Science.gov

Sample records for abundant organic materials

  1. The Abundance and Distribution of Presolar Materials in Cluster IDPS

    NASA Technical Reports Server (NTRS)

    Messenger, Scott; Keller, Lindsay; Nakamura-Messenger, Keiko; Ito, Motoo

    2007-01-01

    Presolar grains and remnants of interstellar organic compounds occur in a wide range of primitive solar system materials, including meteorites, interplanetary dust particles (IDPs), and comet Wild-2 samples. Among the most abundant presolar phases are silicate stardust grains and molecular cloud material. However, these materials have also been susceptible to destruction and alteration during parent body and nebular processing. In addition to their importance as direct samples of remote and ancient astrophysical environments, presolar materials thus provide a measure of how well different primitive bodies have preserved the original solar system starting materials. The matrix normalized abundances of presolar silicate grains in meteorites range from 20 ppm in Semarkona and Bishunpur to 170 ppm for Acfer 094. The lower abundances of presolar silicates in Bishunpur and Semarkona has been ascribed to the destruction of presolar silicates during aqueous processes. Presolar silicates appear to be significantly more abundant in anhydrous IDPs, possibly because these materials did not experience parent body hydrothermal alteration. Among IDPs the estimated abundances of presolar silicates vary by more than an order of magnitude, from 480 to 5500 ppm. The wide disparity in the abundances of presolar silicates of IDPs may be a consequence of the relatively small total area analyzed in those studies and the fine grain sizes of the IDPs. Alternatively, there may be a wide range in presolar silicate abundances between different IDPs. This view is supported by the observation that 15N-rich IDPs have higher presolar silicate abundances than those with isotopically normal N.

  2. The Abundance and Distribution of Presolar Materials in Cluster IDPS

    NASA Technical Reports Server (NTRS)

    Messenger, Scott; Keller, Lindsay; Nakamura-Messenger, Keiko; Ito, Motoo

    2007-01-01

    Presolar grains and remnants of interstellar organic compounds occur in a wide range of primitive solar system materials, including meteorites, interplanetary dust particles (IDPs), and comet Wild-2 samples. Among the most abundant presolar phases are silicate stardust grains and molecular cloud material. However, these materials have also been susceptible to destruction and alteration during parent body and nebular processing. In addition to their importance as direct samples of remote and ancient astrophysical environments, presolar materials thus provide a measure of how well different primitive bodies have preserved the original solar system starting materials.

  3. Porous Organic Molecular Materials

    SciTech Connect

    Tian, Jian; Thallapally, Praveen K.; McGrail, B. Peter

    2012-01-01

    Most nanoporous materials with molecular-scale pores are extended frameworks composed of directional covalent or coordination bonding, such as porous metal-organic frameworks and organic network polymers. By contrast, nanoporous materials comprised of discrete organic molecules, between which there are only weak non-covalent interactions, are seldom encountered. Indeed, most organic molecules pack efficiently in the solid state to minimize the void volume, leading to non-porous materials. In recent years, a significant number of nanoporous organic molecular materials, which may be either crystalline or amorphous, have been confirmed by the studies of gas adsorption and they are surveyed in this Highlight. In addition, the possible advantages of porous organic molecular materials over porous networks are discussed.

  4. Distribution and abundance of organic thiols

    NASA Technical Reports Server (NTRS)

    Fahey, R.

    1985-01-01

    The role of glutathione (GSH) in protecting against the toxicity of oxygen and oxygen by products is well established for all eukaryotes studied except Entamoeba histolytica which lacks mitochrondria, chloroplasts, and microtubules. The GSH is not universal among prokaryotes. Entamoeba histolytica does not produce GSH or key enzymes of GSH metabolism. A general method of thiol analysis based upon fluorescent labeling with monobromobimane and HPLC separation of the resulting thiol derivatives was developed to determine the occurrence of GSH and other low molecular weight thiols in bacteria. Glutathione is the major thiol in cyanobacteria and in most bacteria closely related to the purple photosynthetic bacteria, but GSH was not found in archaebacteria, green bacteria, or GRAM positive bacteria. It suggested that glutathione metabolism was incorporated into eukaryotes at the time that mitochondria and chloroplasts were acquired by endosymbiosis. In Gram positive aerobes, coenzyme A occurs at millimolar levels and CoA disulfide reductases are identified. The CoA, rather than glutathione, may function in the oxygen detoxification processes of these organisms.

  5. Organic nonlinear optical materials

    NASA Technical Reports Server (NTRS)

    Umegaki, S.

    1987-01-01

    Recently, it became clear that organic compounds with delocalized pi electrons show a great nonlinear optical response. Especially, secondary nonlinear optical constants of more than 2 digits were often seen in the molecular level compared to the existing inorganic crystals such as LiNbO3. The crystallization was continuously tried. Organic nonlinear optical crystals have a new future as materials for use in the applied physics such as photomodulation, optical frequency transformation, opto-bistabilization, and phase conjugation optics. Organic nonlinear optical materials, e.g., urea, O2NC6H4NH2, I, II, are reviewed with 50 references.

  6. The Abundance and Isotopic Composition of Hg in Extraterrestrial Materials

    NASA Technical Reports Server (NTRS)

    Lauretta, D. S.

    2004-01-01

    During the past three year grant period we made excellent progress in our study of the abundances and isotopic compositions of Hg and other volatile trace elements in extraterrestrial materials. As part of my startup package I received funds to construct a state-of-the-art experimental facility to study gas-solid reaction kinetics. Much of our effort was spent developing the methodology to measure the abundance and isotopic composition of Hg at ultratrace levels in solid materials. In our first study, the abundance and isotopic composition of Hg was determined in bulk samples of the Murchison (CM) and Allende (CV) carbonaceous chondrites. We have continued our study of mercury in primitive meteorites and expanded the suite of meteorites to include other members of the CM and CV chondrite group as well as CI and CO chondrites. Samples of the CI chondrite Orgueil, the CM chondrites Murray, Nogoya, and Cold Bokkeveld, the CO chondrites Kainsaz, Omans, and Isna, and the CV chondrites Vigarano, Mokoia, and Grosnaja were tested. We have developed a thermal analysis ICP-MS technique and applied it to the study of a suite of thermally labile elements (Zn, As, Se, Cd, In, Sn, Sb, Te, Hg, Au, Tl, Pb, and Bi) in geologic materials as well.

  7. Non-CI refractory lithophile abundances in bulk planetary materials

    NASA Astrophysics Data System (ADS)

    Dauphas, N.

    2015-12-01

    Refractory inclusions in meteorites show evidence for fractionation of refractory lithophile elements relative to one another. For bulk planetary materials, it is most often assumed that refractory lithophile elements (e.g., Ca, Al, Ti, REEs) are in proportions similar to CI carbonaceous chondrites, which is taken to be a proxy for solar composition. A diagnostic feature of REE patterns in refractory inclusions in meteorites is the presence of thulium anomalies, arising from the fact that this heavy REE is more volatile than the highly refractory HREEs surrounding it (Tm/Tm* is defined relative to either Er-Yb or Er-Lu). Tm anomalies thus represent an excellent diagnostic tool to test the assumption that refractory lithophile elements have uniform relative abundances at a bulk planetary scale. Prior to this work, high precision Tm measurements were lacking because it is mono-isotopic and as such is not amenable to high-precision single spike measurements. We have developed a multi-collector REE abundance measurement technique to measure all REEs at high precision, including the mono-isotopic ones. This technique was used to revise the abundance of CI and PAAS REE abundances (Pourmand et al. 2012) and the CI composition agrees well with an independent study (Barrat et al. 2012). The same technique was applied to measure REE patterns in 41 chondrites as well as terrestrial rocks (Dauphas and Pourmand, 2015). Our results reveal the presence of Tm anomalies of about -4.5 % in terrestrial rocks, enstatite and ordinary chondrites, relative to carbonaceous chondrites including CIs. This demonstrates that the assumption that refractory lithophile elements are in constant proportions among planetary bodies is unwarranted. It also shows that carbonaceous chondrites cannot be a major constituent of the Earth. The presence of Tm anomalies in meteorites and terrestrial rocks suggests that either (i) the material in the inner part of the solar system was formed from a gas

  8. Organic materials: Fantastic plastic

    NASA Astrophysics Data System (ADS)

    Gaudiana, Russell; Brabec, Christoph

    2008-05-01

    Polymer materials could bring down the cost of electricity production using photovoltaic technology to below $1 per watt for the first time, and enable mass-market, portable applications for photovoltaic technology.

  9. The Abundance and Isotopic Composition of Hg in Extraterrestrial Materials

    NASA Technical Reports Server (NTRS)

    Blum, J. D.; Klaue, Bjorn

    2005-01-01

    During the three year grant period we made excellent progress in our study of the abundances and isotopic compositions of Hg and other volatile trace elements in extraterrestrial materials. At the time the grant started, our collaborating PI, Dante Lauretts, was a postdoctoral research associate working with Peter Buseck at Arizona State University. The work on chondritic Hg was done in collaboration with Dante Lauretta and Peter Buseck and this study was published in Lauretta et a1 (2001a). In July, 2001 Dante Lauretta accepted a position as an Assistant Professor in the Lunar and Planetary Laboratory at the University of Arizona. His funding was transferred and this grant has supported much of his research activities during his first two years at the U of A. Several other papers are in preparation and will be published soon. We presented papers on this topic at Goldschmidt Conferences, the Lunar and Planetary Science Conferences, and the Annual Meetings of the Meteoritical Society. The work done under this grant has spurred several new directions of inquiry, which we are still pursuing. Included in this paper are the studies of bulk abundances and isotopic compositions of metreoritic Mercury, and the development of a thermal analysis ICP-MS technique applied to thermally liable elements.

  10. Paper Thermoelectrics: Merging Nanotechnology with Naturally Abundant Fibrous Material.

    PubMed

    Sun, Chengjun; Goharpey, Amir Hossein; Rai, Ayush; Zhang, Teng; Ko, Dong-Kyun

    2016-08-31

    The development of paper-based sensors, antennas, and energy-harvesting devices can transform the way electronic devices are manufactured and used. Herein we describe an approach to fabricate paper thermoelectric generators for the first time by directly impregnating naturally abundant cellulose materials with p- or n-type colloidal semiconductor quantum dots. We investigate Seebeck coefficients and electrical conductivities as a function of temperature between 300 and 400 K as well as in-plane thermal conductivities using Angstrom's method. We further demonstrate equipment-free fabrication of flexible thermoelectric modules using p- and n-type paper strips. Leveraged by paper's inherently low thermal conductivity and high flexibility, these paper modules have the potential to efficiently utilize heat available in natural and man-made environments by maximizing the thermal contact to heat sources of arbitrary geometry. PMID:27505304

  11. Oxides for sustainable photovoltaics with earth-abundant materials

    NASA Astrophysics Data System (ADS)

    Wagner, Alexander; Stahl, Mathieu; Ehrhardt, Nikolai; Fahl, Andreas; Ledig, Johannes; Waag, Andreas; Bakin, Andrey

    2014-03-01

    Energy conversion technologies are aiming to extremely high power capacities per year. Nontoxicity and abundance of the materials are the key requirements to a sustainable photovoltaic technology. Oxides are among the key materials to reach these goals. We investigate the influence of thin buffer layers on the performance of an ZnO:Al/buffer/Cu2O solar cells. Introduction of a thin ZnO or Al2O3 buffer layer, grown by thermal ALD, between ZnO:Al and Cu2O resulted in 45% increase of the solar cell efficiency. VPE growth of Cu2O employing elemental copper and pure oxygen as precursor materials is presented. The growth is performed on MgO substrates with the (001) orientation. On- and off- oriented substrates have been employed and the growth results are compared. XRD investigations show the growth of the (110) oriented Cu2O for all temperatures, whereas at a high substrate temperature additional (001) Cu2O growth occurs. An increase of the oxygen partial pressure leads to a more pronounced 2D growth mode, whereby pores between the islands still remain. The implementation of off-axis substrates with 3.5° and 5° does not lead to an improvement of the layer quality. The (110) orientation remains predominant, the grain size decreases and the FWHM of the (220) peak increases. From the AFM images it is concluded, that the (110) surface grows with a tilt angle to the substrate surface.

  12. Organic Materials For Optical Switching

    NASA Technical Reports Server (NTRS)

    Cardelino, Beatriz H.

    1993-01-01

    Equations predict properties of candidate materials. Report presents results of theoretical study of nonlinear optical properties of organic materials. Such materials used in optical switching devices for computers and telecommunications, replacing electronic switches. Optical switching potentially offers extremely high information throughout in compact hardware.

  13. Organic amendments enhance microbial diversity and abundance of functional genes in Australian Soils

    NASA Astrophysics Data System (ADS)

    Aldorri, Sind; McMillan, Mary; Pereg, Lily

    2016-04-01

    Food and cash crops play important roles in Australia's economy with black, grey and red clay soil, widely use for growing cotton, wheat, corn and other crops in rotation. While the majority of cotton growers use nitrogen and phosphate fertilizers only in the form of agrochemicals, a few experiment with the addition of manure or composted plant material before planting. We hypothesized that the use of such organic amendments would enhance the soil microbial function through increased microbial diversity and abundance, thus contribute to improved soil sustainability. To test the hypothesis we collected soil samples from two cotton-growing farms in close geographical proximity and with mostly similar production practices other than one grower has been using composted plants as organic amendment and the second farmer uses only agrochemicals. We applied the Biolog Ecoplate system to study the metabolic signature of microbial communities and used qPCR to estimate the abundance of functional genes in the soil. The soil treated with organic amendments clearly showed higher metabolic activity of a more diverse range of carbon sources as well as higher abundance of genes involved in the nitrogen and phosphorous cycles. Since microbes undertake a large number of soil functions, the use of organic amendments can contribute to the sustainability of agricultural soils.

  14. Plutonium recovery from organic materials

    DOEpatents

    Deaton, R.L.; Silver, G.L.

    1973-12-11

    A method is described for removing plutonium or the like from organic material wherein the organic material is leached with a solution containing a strong reducing agent such as titanium (III) (Ti/sup +3None)/, chromium (II) (Cr/ sup +2/), vanadium (II) (V/sup +2/) ions, or ferrous ethylenediaminetetraacetate (EDTA), the leaching yielding a plutonium-containing solution that is further processed to recover plutonium. The leach solution may also contain citrate or tartrate ion. (Official Gazette)

  15. Organic electroluminescence: materials and devices

    NASA Astrophysics Data System (ADS)

    Kalinowski, Jan

    1996-04-01

    Electroluminescence (EL) inorganics is a phenomenon of both fundamental and practical interest. Defined as direct conversion of electricity into light incorporates many physical processes which are not yet fully understood. Considered originally as an organic analogue of the Destriau effect that is high-field or intrinsic EL found previously in inorganic phosphors, remains still obscure since narrow bands in organic solids rule out electron acceleration to energies allowing impact generation of electronic excited states. Therefore, the search for wide-band organic materials is a challenge to design and to fabricate organic intrinsic EL devices. The recombination radiation following the excess charge carrier injection into a luminescent material stands for injection EL. This type of EL is commonly accepted as a basis for the emission of light from organic materials sandwiched between metal electrodes. In this review, some consequences of the band width and energy level positions in low-molecular weight organic materials and polymers are discussed. Fundamental concepts are illustrated using the notions of recombination ((tau) rec) and transit ((tau) T) times of charge carriers. Injection-controlled ((tau) rec greater than (tau) T) and volume-controlled ((tau) rec less than (tau) T) injection EL modes are distinguished in organic light- emitting-diodes (LEDs). Two routes to fabricate spectrally tunable organic LEDs are discussed: (a) building multilayer devices with various materials as chromophores (emitters) and (b) employing single-layer conjugated polymer systems with different main-chain molecular structures and blending luminescent polymers into the host polymer matrix, or molecularly-doped non-conjugated polymers with appropriate selection of the optically active component. Charge carrier trapping and excitonic interactions are important factors affecting the recombination routes and production of emitting states as is demonstrated on EL from single organic

  16. Self-Organized Porphyrinic Materials

    PubMed Central

    Drain, Charles Michael; Varotto, Alessandro; Radivojevic, Ivana

    2009-01-01

    The self-assembly and self-organization of porphyrins and related macrocycles enables the bottom-up fabrication of photonic materials for fundamental studies of the photophysics of these materials and for diverse applications. This rapidly developing field encompasses a broad range of disciplines including molecular design and synthesis, materials formation and characterization, and the design and evaluation of devices. Since the self-assembly of porphyrins by electrostatic interactions in the late 1980s to the present, there has been an ever increasing degree of sophistication in the design of porphyrins that self-assemble into discrete arrays or self-organize into polymeric systems. These strategies exploit ionic interactions, hydrogen bonding, coordination chemistry, and dispersion forces to form supramolecular systems with varying degrees of hierarchical order. This review concentrates on the methods to form supramolecular porphyrinic systems by intermolecular interactions other than coordination chemistry, the characterization and properties of these photonic materials, and the prospects for using these in devices. The review is heuristically organized by the predominant intermolecular interactions used and emphasizes how the organization affects properties and potential performance in devices. PMID:19253946

  17. Organic electro-optic materials

    NASA Astrophysics Data System (ADS)

    Dalton, Larry R.; Robinson, Bruce H.; Jen, Alex K.; Ried, Philip; Eichinger, Bruce; Jang, Sei-Hum; Luo, Jingdong; Liu, Sen; Liao, Yi; Firestone, Kimberly A.; Bhatambrekar, Nishant P.; Bale, Denise; Haller, Marnie A.; Bhattacharjee, Sanchali; Schendel, Jessica; Sullivan, Philip A.; Hammond, Scott; Buker, Nicholas; Cady, Field; Chen, Antao; Steier, William H.

    2004-12-01

    The potential of organic electro-optic materials for large electro-optic activity and fast response to applied electric fields (leading to 100 GHz device bandwidths) is important and increasingly well-recognized. In this communication, we demonstrate how quantum and statistical mechanical calculations can be used to guide the systematic improvement of both molecular first hyperpolarizability (β) and macroscopic electro-optic activity (r). Femtosecond time-resolved, wavelength-agile Hyper-Rayleigh Scattering (HRS) measurements have been used to measure β values relative to chloroform and to avoid confusion associated with two photon contributions. Electro-optic coefficients have been characterized by simple reflection (Teng-Man method), attenuated total reflection (ATR), and Mach Zehnder interferometry. "Constant bias" modifications of these techniques have been used to permit investigation of optimized poling conditions. Organic electro-optic materials also afford unique advantages for the fabrication of conformal and flexible devices, for the integration of disparate materials, and for exploitation of novel manufacturing technologies such as soft lithography. Both stripline and ring microresonator structures have been fabricated by soft lithography. The integration of organic electro-optic materials with silicon photonics (both split ring microresonators and photonic bandgap circuitry) has been demonstrated.

  18. EELS from organic crystalline materials

    NASA Astrophysics Data System (ADS)

    Brydson, R.; Eddleston, M. D.; Jones, W.; Seabourne, C. R.; Hondow, N.

    2014-06-01

    We report the use of the electron energy loss spectroscopy (EELS) for providing light element chemical composition information from organic, crystalline pharmaceutical materials including theophylline and paracetamol and discuss how this type of data can complement transmission electron microscopy (TEM) imaging and electron diffraction when investigating polymorphism. We also discuss the potential for the extraction of bonding information using electron loss near-edge structure (ELNES).

  19. Water permeation through organic materials

    NASA Astrophysics Data System (ADS)

    Doughty, D. H.; West, I. A.

    1981-09-01

    Atmospheric moisture is routinely excluded from weapon systems by the use of elastomer seals at assembly joints and electrical feedthroughs while internal moisture is minimized by relying on desiccants and on pre-dried components assembled in special low humidity assembly rooms. Published values of the water permeation coefficient for ethylene-propylene rubber and other o-ring materials are subject to some variability and the effects of aging on water permability are unknown. We have thus devised a new and extremely sensitive method for measuring moisture permeation coefficients in organic materials. This method uses dilute tritiated water as a tracer and it is approximately two orders of magnitude more sensitive than other methods. We are therefore able to make measurements on materials under STS temperature and humidity conditions. Rate data showing the approach to equilibrium and water permeability values for a variety of elastomers are presented. The test apparatus is also described.

  20. Anatomy of a cluster IDP. Part 2: Noble gas abundances, trace element geochemistry, isotopic abundances, and trace organic chemistry of several fragments from L2008#5

    NASA Technical Reports Server (NTRS)

    Thomas, K. L.; Clemett, S. J.; Flynn, G. J.; Keller, L. P.; Mckay, David S.; Messenger, S.; Nier, A. O.; Schlutter, D. J.; Sutton, S. R.; Walker, R. M.

    1994-01-01

    The topics discussed include the following: noble gas content and release temperatures; trace element abundances; heating summary of cluster fragments; isotopic measurements; and trace organic chemistry.

  1. Solid Suspension Flow Batteries Using Earth Abundant Materials.

    PubMed

    Mubeen, Syed; Jun, Young-Si; Lee, Joun; McFarland, Eric W

    2016-01-27

    The technical features of solid-electrode batteries (e.g., high energy density, relatively low capital cost ($/kWh)) and flow batteries (e.g., long cycle life, design flexibility) are highly complementary. It is therefore extremely desirable to integrate their advantages into a single storage device for large-scale energy storage applications where lifetime cost ($/kW-h/cycle) is an extremely important parameter. Here, we demonstrate a non-Li-based-flow battery concept that replaces the aqueous solution of redox-active molecules found in typical redox flow batteries with suspensions of hydrophilic carbon particles ("solid suspension electrodes") coated with earth-abundant redox-active metals. The solid suspension electrodes charge by depositing earth-abundant redox-active metals onto the carbon particle suspension, which are then stripped during discharge operation. The electrical contact to the solid suspension electrodes is fed through fixed redox-inert hydrophobic carbon current collectors through "contact charge transfer" mechanism. The hydrophobicity of the current collectors prevents direct plating of redox-active metals onto their surfaces. The above concept was successfully used to demonstrate several non-Li-based battery chemistries including zinc-copper, zinc-manganese oxide, zinc-bromine, and zinc-sulfur, providing a pathway for potential applications in medium and large-scale electrical energy storage. PMID:26727225

  2. 13 ENDOR studies of organic radicals in natural isotopic abundance

    NASA Astrophysics Data System (ADS)

    Kirste, Burkhard

    13C ENDOR studies of phenoxyls, galvinoxyls, triphenylmethyl radicals, nitroxides, and cyclosilane and semiquinone radical anions with natural isotopic distribution are reported. The method is described, and it is shown that 13C coupling constants can be measured precisely; in favorable cases even the determination of signs is possible by general TRIPLE resonance. Studies of the relaxation behavior of 13C ENDOR signals or measurements of hyperfine shifts in liquid-crystalline solutions yield information about dipolar hyperfine interactions and hence π spin populations which is of aid in assignments to molecular positions. Complete sets of 13C coupling constants have been determined for 2,4,6-tri- tert-butylphenoxyl and Coppinger's radical. For the central carbon atoms of tert-butyl groups, a Q parameter of Qτ-Bu C = -34 MHz is proposed, and for a 29Si atom in trimethylsilyl groups, QTMSSi = +49 MHz. Favorable conditions for natural-abundance 13C ENDOR experiments, e.g., small hyperfine anisotropies and use of deuterated compounds, and limitations of the method are discussed.

  3. Spectral abundance fraction estimation of materials using Kalman filters

    NASA Astrophysics Data System (ADS)

    Wang, Su; Chang, Chein; Jensen, Janet L.; Jensen, James O.

    2004-12-01

    Kalman filter has been widely used in statistical signal processing for parameter estimation. Although a Kalman filter approach has been recently developed for spectral unmixing, referred to as Kalman filter-based linear unmixing (KFLU), its applicability to spectral characterization within a single pixel vector has not been explored. This paper presents a new application of Kalman filtering in spectral estimation and quantification. It develops a Kalman filter-based spectral signature esimator (KFSSE) which is different from the KFLU in the sense that the former performs a Kalman filter wavelength by wavelength across a spectral signature as opposed to the latter which implements a Kalman filter pixel vector by pixel vector in an image cube. The idea of the KFSSE is to implement the state equation to characterize the true spectral signature, while the measurement equation is being used to describe the spectral signature to be processed. Additionally, since a Kalman filter can accurately estimate spectral abundance fraction of a signature, our proposed KFSSE can further used for spectral quantification for subpixel targets and mixed pixel vectors, called Kalman filter-based spectral quantifier (KFSQ). Such spectral quantification is particularly important for chemical/biological defense which requires quantification of detected agents for damage control assessment. Several different types of hyperspectral data are used for experiments to demonstrate the ability of the KFSSE in estimation of spectral signature and the utility of the KFSQ in spectral quantification.

  4. Organic materials for electronic devices

    NASA Astrophysics Data System (ADS)

    Zeng, Lichang

    Through light absorption and emission as well as charge carrier generation, transport and recombination, pi-conjugated molecules are central to electronic devices including organic field-effect transistors, organic light-emitting diodes, and organic solar cells. This thesis reports on materials development via molecular design, material synthesis and processing, device fabrication and characterization. Major accomplishments are summarized as follows. A series of oligo(fluorene-co-bithiophene)s, OF2Ts, have been synthesized and characterized for an investigation of the effects of oligomer length and pendant aliphatic structure on thermotropic properties, light absorption and emission, and anisotropic field-effect mobilities. Solvent-vapor annealing at room temperature was shown to be capable of orienting OF2Ts into monodomain glassy-nematic films with an orientational order parameter emulating that achieved with conventional thermal annealing on a rubbed polyimide alignment layer. Comprising hole- and electron-transporting moieties with flexible linkages, non-conjugated bipolar compounds have been developed for use as hosts for electrophosphorescence. These materials are characterized by an elevated glass transition temperature, morphological stability against crystallization, LUMO and HOMO levels unaffected by chemical bonding, and triplet energy unconstrained by the electrochemical energy gap. Phosphorescent OLEDs containing solution-processed emitting layers were fabricated with TRZ-3Cz(MP)2, TRZ-1Cz(MP)2 and Cz(MP)2 hosting Ir(mppy)3 for an illustration of how chemical composition and hence charge transport properties affect device performance. Bulk heterojunction organic solar cells comprising an active layer of P3HT:PCBM blend at a 1:1 mass ratio with thickness from 130 to 1200 mn have been fabricated and characterized before and after thermal annealing. Before thermal annealing, both short circuit current density and power conversion efficiency decrease with

  5. Functional organic materials for electronics industries

    NASA Technical Reports Server (NTRS)

    Shibayama, K.; Ono, H.

    1982-01-01

    Topics closely related with organic, high molecular weight material synthesis are discussed. These are related to applications such as display, recording, sensors, semiconductors, and I.C. correlation. New materials are also discussed. General principles of individual application are not included. Materials discussed include color, electrochromic, thermal recording, organic photoconductors for electrophotography, and photochromic materials.

  6. The activated sludge ecosystem contains a core community of abundant organisms

    PubMed Central

    Saunders, Aaron M; Albertsen, Mads; Vollertsen, Jes; Nielsen, Per H

    2016-01-01

    Understanding the microbial ecology of a system requires that the observed population dynamics can be linked to their metabolic functions. However, functional characterization is laborious and the choice of organisms should be prioritized to those that are frequently abundant (core) or transiently abundant, which are therefore putatively make the greatest contribution to carbon turnover in the system. We analyzed the microbial communities in 13 Danish wastewater treatment plants with nutrient removal in consecutive years and a single plant periodically over 6 years, using Illumina sequencing of 16S ribosomal RNA amplicons of the V4 region. The plants contained a core community of 63 abundant genus-level operational taxonomic units (OTUs) that made up 68% of the total reads. A core community consisting of abundant OTUs was also observed within the incoming wastewater to three plants. The net growth rate for individual OTUs was quantified using mass balance, and it was found that 10% of the total reads in the activated sludge were from slow or non-growing OTUs, and that their measured abundance was primarily because of immigration with the wastewater. Transiently abundant organisms were also identified. Among them the genus Nitrotoga (class Betaproteobacteria) was the most abundant putative nitrite oxidizer in a number of activated sludge plants, which challenges previous assumptions that Nitrospira (phylum Nitrospirae) are the primary nitrite-oxidizers in activated sludge systems with nutrient removal. PMID:26262816

  7. NREL Explores Earth-Abundant Materials for Future Solar Cells (Fact Sheet)

    SciTech Connect

    Not Available

    2012-10-01

    Researchers at the National Renewable Energy Laboratory (NREL) are using a theory-driven technique - sequential cation mutation - to understand the nature and limitations of promising solar cell materials that can replace today's technologies. Finding new materials that use Earth-abundant elements and are easily manufactured is important for large-scale solar electricity deployment.

  8. Consequences of organic farming and landscape heterogeneity for species richness and abundance of farmland birds.

    PubMed

    Smith, Henrik G; Dänhardt, Juliana; Lindström, Ake; Rundlöf, Maj

    2010-04-01

    It has been suggested that organic farming may benefit farmland biodiversity more in landscapes that have lost a significant part of its former landscape heterogeneity. We tested this hypothesis by comparing bird species richness and abundance during the breeding season in organic and conventional farms, matched to eliminate all differences not directly linked to the farming practice, situated in either homogeneous plains with only a little semi-natural habitat or in heterogeneous farmland landscapes with abundant field borders and semi-natural grasslands. The effect of farm management on species richness interacted with landscape structure, such that there was a positive relationship between organic farming and diversity only in homogeneous landscapes. This pattern was mainly dependent on the species richness of passerine birds, in particular those that were invertebrate feeders. Species richness of non-passerines was positively related to organic farming independent of the landscape context. Bird abundance was positively related to landscape heterogeneity but not to farm management. This was mainly because the abundance of passerines, particularly invertebrate feeders, was positively related to landscape heterogeneity. We suggest that invertebrate feeders particularly benefit from organic farming because of improved foraging conditions through increased invertebrate abundances in otherwise depauperate homogeneous landscapes. Although many seed-eaters also benefit from increased insect abundance, they may also utilize crop seed resources in homogeneous landscapes and conventional farms. The occurrence of an interactive effect of organic farming and landscape heterogeneity on bird diversity will have consequences for the optimal allocation of resources to restore the diversity of farmland birds. PMID:20213151

  9. Novel High Efficient Organic Photovoltaic Materials

    NASA Technical Reports Server (NTRS)

    Sun, Sam; Haliburton, James; Fan, Zben; Taft, Charles; Wang, Yi-Qing; Maaref, Shahin; Mackey, Willie R. (Technical Monitor)

    2001-01-01

    In man's mission to the outer space or a remote site, the most abundant, renewable, nonpolluting, and unlimited external energy source is light. Photovoltaic (PV) materials can convert light into electrical power. In order to generate appreciable electrical power in space or on the Earth, it is necessary to collect sunlight from large areas due to the low density of sunlight, and this would be very costly using current commercially available inorganic solar cells. Future organic or polymer based solar cells seemed very attractive due to several reasons. These include lightweight, flexible shape, ultra-fast optoelectronic response time (this also makes organic PV materials attractive for developing ultra-fast photo detectors), tunability of energy band-gaps via molecular design, versatile materials synthesis and device fabrication schemes, and much lower cost on large-scale industrial production. It has been predicted that nano-phase separated block copolymer systems containing electron rich donor blocks and electron deficient acceptor blocks will facilitate the charge separation and migration due to improved electronic ultrastructure and morphology in comparison to current polymer composite photovoltaic system. This presentation will describe our recent progress in the design, synthesis and characterization of a novel donor-bridge-acceptor block copolymer system for potential high-efficient organic optoelectronic applications. Specifically, the donor block contains an electron donating alkyloxy derivatized polyphenylenevinylene, the acceptor block contains an electron withdrawing alkyl-sulfone derivatized polyphenylenevinylene, and the bridge block contains an electronically neutral non-conjugated aliphatic hydrocarbon chain. The key synthetic strategy includes the synthesis of each individual block first, then couple the blocks together. While the donor block stabilizes the holes, the acceptor block stabilizes the electrons. The bridge block is designed to hinder

  10. Method for catalytic destruction of organic materials

    DOEpatents

    Sealock, L.J. Jr.; Baker, E.G.; Elliott, D.C.

    1997-05-20

    A method is disclosed for converting waste organic materials into an innocuous product gas. The method comprises maintaining, in a pressure vessel, in the absence of oxygen, at a temperature of 250 to 500 C and a pressure of at least 50 atmospheres, a fluid organic waste material, water, and a catalyst consisting essentially of reduced nickel in an amount sufficient to catalyze a reaction of the organic waste material to produce an innocuous product gas composed primarily of methane and carbon dioxide. The methane in the product gas may be burned to preheat the organic materials. 7 figs.

  11. Method for catalytic destruction of organic materials

    DOEpatents

    Sealock, Jr., L. John; Baker, Eddie G.; Elliott, Douglas C.

    1997-01-01

    A method is disclosed for converting waste organic materials into an innocuous product gas. The method comprises maintaining, in a pressure vessel, in the absence of oxygen, at a temperature of 250.degree. C. to 500.degree. C. and a pressure of at least 50 atmospheres, a fluid organic waste material, water, and a catalyst consisting essentially of reduced nickel in an amount sufficient to catalyze a reaction of the organic waste material to produce an innocuous product gas composed primarily of methane and carbon dioxide. The methane in the product gas may be burned to preheat the organic materials.

  12. SEASONAL ABUNDANCE OF ORGANIC MOLECULAR MARKERS IN URBAN PARTICULATE MATTER FROM PHILADELPHIA, PA

    EPA Science Inventory

    Organic molecular markers were measured in airborne particulate matter (PM10) from the City of Philadelphia North Broad Street air quality monitoring site to identify the seasonal abundances of key tracer compounds together with their dominant sources. Daily PM10...

  13. Determining carbon-carbon connectivities in natural abundance organic powders using dipolar couplings.

    PubMed

    Dekhil, Myriam; Mollica, Giulia; Bonniot, Tristan Texier; Ziarelli, Fabio; Thureau, Pierre; Viel, Stéphane

    2016-06-30

    We present a solid-state NMR methodology capable of investigating the carbon skeleton of natural abundance organic powders. The methodology is based on the (13)C-(13)C dipolar coupling interaction and allows carbon-carbon connectivities to be unambiguously established for a wide range of organic solids. This methodology is particularly suitable for disordered solids, such as natural or synthetic macromolecules, which cannot be studied using conventional diffraction or NMR techniques. PMID:27319808

  14. Purification of metal-organic framework materials

    SciTech Connect

    Farha, Omar K.; Hupp, Joseph T.

    2012-12-04

    A method of purification of a solid mixture of a metal-organic framework (MOF) material and an unwanted second material by disposing the solid mixture in a liquid separation medium having a density that lies between those of the wanted MOF material and the unwanted material, whereby the solid mixture separates by density differences into a fraction of wanted MOF material and another fraction of unwanted material.

  15. Purification of metal-organic framework materials

    SciTech Connect

    Farha, Omar K.; Hupp, Joseph T.

    2015-06-30

    A method of purification of a solid mixture of a metal-organic framework (MOF) material and an unwanted second material by disposing the solid mixture in a liquid separation medium having a density that lies between those of the wanted MOF material and the unwanted material, whereby the solid mixture separates by density differences into a fraction of wanted MOF material and another fraction of unwanted material.

  16. Organic matter formed from hydrolysis of metal carbides of the iron peak of cosmic elemental abundance

    NASA Astrophysics Data System (ADS)

    Cataldo, Franco

    2003-01-01

    This work is a modern revisitation of an old idea of great chemists of the past such as Berthelot, Mendeleev, Cloez and Moissan: the formation of organic matter under pre-biotic conditions starting from the hydrolysis of metal carbides. This idea was originally proposed for the formation of petroleum in the Earth and was extended to other bodies of the solar system by Sokolov at the end of the 19th century. The reason for this revisitation lies in the fact that complex organic matter resembling a petroleum fraction may exist in certain protoplanetary nebulae. The present work starts with a survey of the theory of the inorganic origin of petroleum and reports on current evidence for its derivation from residues of formerly living matter, but also considers theories that admit both a biogenic and an abiogenic origin for petroleum. By considering the cosmic abundance of elements and the evidence concerning the presence of carbides in meteorites, we discuss the formation, structure and hydrolysis products derived from the metal carbides of the iron peak of cosmic elemental abundance. Chromium carbide (Cr3C2) has then been used as a model compound for all the key carbides of the iron peak of the cosmic abundance (Cr, Fe, Ni, V, Mn, Co) and it has been hydrolysed under different conditions and the hydrocarbons formed have been analysed using electronic spectroscopy, high-performance liquid chromatography with a diode-array detector (HPLC-DAD) and by Fourier-transform infrared (FT-IR) spectroscopy. Methane, a series of about 20 different alkenes with single and conjugated double bonds have been detected. Paraffins are formed simultaneously with the alkene series but no acetylenic hydrocarbons have been detected. This study confirms early works considering the easy hydrolysis of the carbides of Cr, Fe, Ni, Mn and Co with the formation of H2, a series of alkanes including methane and a series of alkenes including ethylene. The peculiar behaviour of copper carbide (copper is

  17. Apparatus and method for oxidizing organic materials

    DOEpatents

    Surma, J.E.; Bryan, G.H.; Geeting, J.G.H.; Butner, R.S.

    1998-01-13

    The invention is a method and apparatus using high cerium concentration in the anolyte of an electrochemical cell to oxidize organic materials. The method and apparatus further use an ultrasonic mixer to enhance the oxidation rate of the organic material in the electrochemical cell. 6 figs.

  18. Apparatus and method for oxidizing organic materials

    DOEpatents

    Surma, Jeffrey E.; Bryan, Garry H.; Geeting, John G. H.; Butner, R. Scott

    1998-01-01

    The invention is a method and apparatus using high cerium concentration in the anolyte of an electrochemical cell to oxidize organic materials. The method and apparatus further use an ultrasonic mixer to enhance the oxidation rate of the organic material in the electrochemical cell.

  19. Spiers memorial lecture. Organic electronics: an organic materials perspective.

    PubMed

    Wudl, Fred

    2014-01-01

    This Introductory Lecture is intended to provide a background to Faraday Discussion 174: "Organic Photonics and Electronics" and will consist of a chronological, subjective review of organic electronics. Starting with "ancient history" (1888) and history (1950-present), the article will take us to the present. The principal developments involved the processes of charge carrier generation and charge transport in molecular solids, starting with insulators (photoconductors) and moving to metals, to semiconductors and ending with the most popular semiconductor devices, such as organic light-emitting diodes (OLEDs), organic field effect transistors (OFETs) and organic photovoltaics (OPVs). The presentation will be from an organic chemistry/materials point of view. PMID:25354490

  20. Organic Matter Degradation Drives Benthic Cyanobacterial Mat Abundance on Caribbean Coral Reefs

    PubMed Central

    Brocke, Hannah J.; Polerecky, Lubos; de Beer, Dirk; Weber, Miriam; Claudet, Joachim; Nugues, Maggy M.

    2015-01-01

    Benthic cyanobacterial mats (BCMs) are impacting coral reefs worldwide. However, the factors and mechanisms driving their proliferation are unclear. We conducted a multi-year survey around the Caribbean island of Curaçao, which revealed highest BCM abundance on sheltered reefs close to urbanised areas. Reefs with high BCM abundance were also characterised by high benthic cover of macroalgae and low cover of corals. Nutrient concentrations in the water-column were consistently low, but markedly increased just above substrata (both sandy and hard) covered with BCMs. This was true for sites with both high and low BCM coverage, suggesting that BCM growth is stimulated by a localised, substrate-linked release of nutrients from the microbial degradation of organic matter. This hypothesis was supported by a higher organic content in sediments on reefs with high BCM coverage, and by an in situ experiment which showed that BCMs grew within days on sediments enriched with organic matter (Spirulina). We propose that nutrient runoff from urbanised areas stimulates phototrophic blooms and enhances organic matter concentrations on the reef. This organic matter is transported by currents and settles on the seabed at sites with low hydrodynamics. Subsequently, nutrients released from the organic matter degradation fuel the growth of BCMs. Improved management of nutrients generated on land should lower organic loading of sediments and other benthos (e.g. turf and macroalgae) to reduce BCM proliferation on coral reefs. PMID:25941812

  1. Organic matter degradation drives benthic cyanobacterial mat abundance on Caribbean coral reefs.

    PubMed

    Brocke, Hannah J; Polerecky, Lubos; de Beer, Dirk; Weber, Miriam; Claudet, Joachim; Nugues, Maggy M

    2015-01-01

    Benthic cyanobacterial mats (BCMs) are impacting coral reefs worldwide. However, the factors and mechanisms driving their proliferation are unclear. We conducted a multi-year survey around the Caribbean island of Curaçao, which revealed highest BCM abundance on sheltered reefs close to urbanised areas. Reefs with high BCM abundance were also characterised by high benthic cover of macroalgae and low cover of corals. Nutrient concentrations in the water-column were consistently low, but markedly increased just above substrata (both sandy and hard) covered with BCMs. This was true for sites with both high and low BCM coverage, suggesting that BCM growth is stimulated by a localised, substrate-linked release of nutrients from the microbial degradation of organic matter. This hypothesis was supported by a higher organic content in sediments on reefs with high BCM coverage, and by an in situ experiment which showed that BCMs grew within days on sediments enriched with organic matter (Spirulina). We propose that nutrient runoff from urbanised areas stimulates phototrophic blooms and enhances organic matter concentrations on the reef. This organic matter is transported by currents and settles on the seabed at sites with low hydrodynamics. Subsequently, nutrients released from the organic matter degradation fuel the growth of BCMs. Improved management of nutrients generated on land should lower organic loading of sediments and other benthos (e.g. turf and macroalgae) to reduce BCM proliferation on coral reefs. PMID:25941812

  2. Organic thermoelectric materials: emerging green energy materials converting heat to electricity directly and efficiently.

    PubMed

    Zhang, Qian; Sun, Yimeng; Xu, Wei; Zhu, Daoben

    2014-10-29

    The abundance of solar thermal energy and the widespread demands for waste heat recovery make thermoelectric generators (TEGs) very attractive in harvesting low-cost energy resources. Meanwhile, thermoelectric refrigeration is promising for local cooling and niche applications. In this context there is currently a growing interest in developing organic thermoelectric materials which are flexible, cost-effective, eco-friendly and potentially energy-efficient. In particular, the past several years have witnessed remarkable progress in organic thermoelectric materials and devices. In this review, thermoelectric properties of conducting polymers and small molecules are summarized, with recent progresses in materials, measurements and devices highlighted. Prospects and suggestions for future research efforts are also presented. The organic thermoelectric materials are emerging candidates for green energy conversion. PMID:24687930

  3. Secondary Ion Mass Spectrometry of Zeolite Materials: Observation of Abundant Aluminosilicate Oligomers Using an Ion Trap

    SciTech Connect

    Groenewold, Gary Steven; Kessinger, Glen Frank; Scott, Jill Rennee; Gianotto, Anita Kay; Appelhans, Anthony David; Delmore, James Edward

    2000-12-01

    Oligomeric oxyanions were observed in the secondary ion mass spectra (SIMS) of zeolite materials. The oxyanions have the general composition AlmSinO2(m+n)H(m-1)- (m + n = 2 to 8) and are termed dehydrates. For a given mass, multiple elemental compositions are possible because (Al + H) is an isovalent and isobaric substitute for Si. Using 18 keV Ga+ as a projectile, oligomer abundances are low relative to the monomers. Oligomer abundance can be increased by using the polyatomic projectile ReO4- (~5 keV). Oligomer abundance can be further increased using an ion trap (IT-) SIMS; in this instrument, long ion lifetimes (tens of ms) and relatively high He pressure result in significant collisional stabilization and increased high-mass abundance. The dehydrates rapidly react with adventitious H2O present in the IT-SIMS to form mono-, di-, and trihydrates. The rapidity of the reaction and comparison to aluminum oxyanion hydration suggest that H2O adds to the aluminosilicate oxyanions in a dissociative fashion, forming covalently bound product ions. In addition to these findings, it was noted that production of abundant oligomeric aluminosilicates could be significantly increased by substituting the countercation (NH4+) with the larger alkali ions Rb+ and Cs+. This constitutes a useful tactic for generating large aluminosilicate oligomers for surface characterization and ion-molecule reactivity studies.

  4. Recent advances in organic semiconducting materials

    NASA Astrophysics Data System (ADS)

    Ostroverkhova, Oksana

    2011-10-01

    Organic semiconductors have attracted attention due to their low cost, easy fabrication, and tunable properties. Applications of organic materials in thin-film transistors, solar cells, light-emitting diodes, sensors, and many other devices have been actively explored. Recent advances in organic synthesis, material processing, and device fabrication led to significant improvements in (opto)electronic device performance. However, a number of challenges remain. These range from lack of understanding of basic physics of intermolecular interactions that determine optical and electronic properties of organic materials to difficulties in controlling film morphology and stability. In this presentation, current state of the field will be reviewed and recent results related to charge carrier and exciton dynamics in organic thin films will be presented.[4pt] In collaboration with Whitney Shepherd, Mark Kendrick, Andrew Platt, Oregon State University; Marsha Loth and John Anthony, University of Kentucky.

  5. Hydrophobic Porous Material Adsorbs Small Organic Molecules

    NASA Technical Reports Server (NTRS)

    Sharma, Pramod K.; Hickey, Gregory S.

    1994-01-01

    Composite molecular-sieve material has pore structure designed specifically for preferential adsorption of organic molecules for sizes ranging from 3 to 6 angstrom. Design based on principle that contaminant molecules become strongly bound to surface of adsorbent when size of contaminant molecules is nearly same as that of pores in adsorbent. Material used to remove small organic contaminant molecules from vacuum systems or from enclosed gaseous environments like closed-loop life-support systems.

  6. Interaction of pesticides with natural organic material

    USGS Publications Warehouse

    Wershaw, R. L.; Burcar, P.J.; Goldberg, M.C.

    1969-01-01

    Two examples of the interaction of pesticides with natural organic materials have been investigated. Sodium humate solubilizes DDT in water and humic acid strongly sorbs 2,4,5-T. These two types of interactions are indicative of the types that one would expect when any organic pesticide is applied to a natural soil-water system.

  7. Organic Nitrogen-Driven Stimulation of Arbuscular Mycorrhizal Fungal Hyphae Correlates with Abundance of Ammonia Oxidizers.

    PubMed

    Bukovská, Petra; Gryndler, Milan; Gryndlerová, Hana; Püschel, David; Jansa, Jan

    2016-01-01

    Large fraction of mineral nutrients in natural soil environments is recycled from complex and heterogeneously distributed organic sources. These sources are explored by both roots and associated mycorrhizal fungi. However, the mechanisms behind the responses of arbuscular mycorrhizal (AM) hyphal networks to soil organic patches of different qualities remain little understood. Therefore, we conducted a multiple-choice experiment examining hyphal responses to different soil patches within the root-free zone by two AM fungal species (Rhizophagus irregularis and Claroideoglomus claroideum) associated with Medicago truncatula, a legume forming nitrogen-fixing root nodules. Hyphal colonization of the patches was assessed microscopically and by quantitative real-time PCR (qPCR) using AM taxon-specific markers, and the prokaryotic and fungal communities in the patches (pooled per organic amendment treatment) were profiled by 454-amplicon sequencing. Specific qPCR markers were then designed and used to quantify the abundance of prokaryotic taxa showing the strongest correlation with the pattern of AM hyphal proliferation in the organic patches as per the 454-sequencing. The hyphal density of both AM fungi increased due to nitrogen (N)-containing organic amendments (i.e., chitin, DNA, albumin, and clover biomass), while no responses as compared to the non-amended soil patch were recorded for cellulose, phytate, or inorganic phosphate amendments. Abundances of several prokaryotes, including Nitrosospira sp. (an ammonium oxidizer) and an unknown prokaryote with affiliation to Acanthamoeba endosymbiont, which were frequently recorded in the 454-sequencing profiles, correlated positively with the hyphal responses of R. irregularis to the soil amendments. Strong correlation between abundance of these two prokaryotes and the hyphal responses to organic soil amendments by both AM fungi was then confirmed by qPCR analyses using all individual replicate patch samples. Further

  8. Organic Nitrogen-Driven Stimulation of Arbuscular Mycorrhizal Fungal Hyphae Correlates with Abundance of Ammonia Oxidizers

    PubMed Central

    Bukovská, Petra; Gryndler, Milan; Gryndlerová, Hana; Püschel, David; Jansa, Jan

    2016-01-01

    Large fraction of mineral nutrients in natural soil environments is recycled from complex and heterogeneously distributed organic sources. These sources are explored by both roots and associated mycorrhizal fungi. However, the mechanisms behind the responses of arbuscular mycorrhizal (AM) hyphal networks to soil organic patches of different qualities remain little understood. Therefore, we conducted a multiple-choice experiment examining hyphal responses to different soil patches within the root-free zone by two AM fungal species (Rhizophagus irregularis and Claroideoglomus claroideum) associated with Medicago truncatula, a legume forming nitrogen-fixing root nodules. Hyphal colonization of the patches was assessed microscopically and by quantitative real-time PCR (qPCR) using AM taxon-specific markers, and the prokaryotic and fungal communities in the patches (pooled per organic amendment treatment) were profiled by 454-amplicon sequencing. Specific qPCR markers were then designed and used to quantify the abundance of prokaryotic taxa showing the strongest correlation with the pattern of AM hyphal proliferation in the organic patches as per the 454-sequencing. The hyphal density of both AM fungi increased due to nitrogen (N)-containing organic amendments (i.e., chitin, DNA, albumin, and clover biomass), while no responses as compared to the non-amended soil patch were recorded for cellulose, phytate, or inorganic phosphate amendments. Abundances of several prokaryotes, including Nitrosospira sp. (an ammonium oxidizer) and an unknown prokaryote with affiliation to Acanthamoeba endosymbiont, which were frequently recorded in the 454-sequencing profiles, correlated positively with the hyphal responses of R. irregularis to the soil amendments. Strong correlation between abundance of these two prokaryotes and the hyphal responses to organic soil amendments by both AM fungi was then confirmed by qPCR analyses using all individual replicate patch samples. Further

  9. Chemoselective single-site Earth-abundant metal catalysts at metal-organic framework nodes.

    PubMed

    Manna, Kuntal; Ji, Pengfei; Lin, Zekai; Greene, Francis X; Urban, Ania; Thacker, Nathan C; Lin, Wenbin

    2016-01-01

    Earth-abundant metal catalysts are critically needed for sustainable chemical synthesis. Here we report a simple, cheap and effective strategy of producing novel earth-abundant metal catalysts at metal-organic framework (MOF) nodes for broad-scope organic transformations. The straightforward metalation of MOF secondary building units (SBUs) with cobalt and iron salts affords highly active and reusable single-site solid catalysts for a range of organic reactions, including chemoselective borylation, silylation and amination of benzylic C-H bonds, as well as hydrogenation and hydroboration of alkenes and ketones. Our structural, spectroscopic and kinetic studies suggest that chemoselective organic transformations occur on site-isolated, electron-deficient and coordinatively unsaturated metal centres at the SBUs via σ-bond metathesis pathways and as a result of the steric environment around the catalytic site. MOFs thus provide a novel platform for the development of highly active and affordable base metal catalysts for the sustainable synthesis of fine chemicals. PMID:27574182

  10. Future Sources of Organic Raw Materials.

    ERIC Educational Resources Information Center

    Shapiro, Irving S.

    1978-01-01

    Examines the need for industrial organization, academic institutions, and national governments to agree on cooperative roles in planning the future raw materials demands of the chemical industry. Political and social concerns, as well as technical and economic considerations, are important to the raw material future of the industry. (MA)

  11. Protective glove material permeation by organic solids.

    PubMed

    Fricker, C; Hardy, J K

    1992-12-01

    A method has been developed for the determination of permeation characteristics of glove materials by organic solids. The system employs a stainless steel exposure cell and allows rapid and uniform contact of either solid disks or powders with minimal membrane bowing. A gas chromatograph equipped with a flame ionization detector was used for monitoring the permeation process, which provided detection limits of 0.9-1.2 ng for the organic solids evaluated. By using an automated system for instrument control and data collection, breakthrough times, steady-state times, and steady-state permeation rates have been determined for five common glove materials when exposed to nine organic solids. PMID:1471595

  12. Constraining the Abundances of Complex Organics in the Inner Regions of Solar-Type Protostars

    NASA Astrophysics Data System (ADS)

    López-Sepulcre, A.; Taquet, V.; Ceccarelli, C.; Neri, R.; Kahane, C.; Charnley, S. B.

    2015-12-01

    We present arcsecond-resolution observations, obtained with the IRAM Plateau de Bure interferometer, of multiple complex organic molecules in two hot corino protostars: IRAS 2A and IRAS 4A, in the NGC 1333 star-forming region. The distribution of the line emission is very compact, indicating the presence of COMs is mostly concentrated in the inner hot corino regions. A comparison of the COMs abundances with astrochemical models favours a gas-phase formation route for CH3OCH3, and a grain formation of C2H5OH, C2H5CN, and HCOCH2OH. The high abundances of methyl formate (HCOOCH3) remain underpredicted by an order of magnitude.

  13. High-resolution NMR of hydrogen in organic solids by DNP enhanced natural abundance deuterium spectroscopy

    NASA Astrophysics Data System (ADS)

    Rossini, Aaron J.; Schlagnitweit, Judith; Lesage, Anne; Emsley, Lyndon

    2015-10-01

    We demonstrate that high field (9.4 T) dynamic nuclear polarization (DNP) at cryogenic (∼100 K) sample temperatures enables the rapid acquisition of natural abundance 1H-2H cross-polarization magic angle spinning (CPMAS) solid-state NMR spectra of organic solids. Spectra were obtained by impregnating substrates with a solution of the stable DNP polarizing agent TEKPol in tetrachloroethane. Tetrachloroethane is a non-solvent for the solids, and the unmodified substrates are then polarized through spin diffusion. High quality natural abundance 2H CPMAS spectra of histidine hydrochloride monohydrate, glycylglycine and theophylline were acquired in less than 2 h, providing direct access to hydrogen chemical shifts and quadrupolar couplings. The spectral resolution of the 2H solid-state NMR spectra is comparable to that of 1H spectra obtained with state of the art homonuclear decoupling techniques.

  14. High-resolution NMR of hydrogen in organic solids by DNP enhanced natural abundance deuterium spectroscopy.

    PubMed

    Rossini, Aaron J; Schlagnitweit, Judith; Lesage, Anne; Emsley, Lyndon

    2015-10-01

    We demonstrate that high field (9.4 T) dynamic nuclear polarization (DNP) at cryogenic (∼100 K) sample temperatures enables the rapid acquisition of natural abundance (1)H-(2)H cross-polarization magic angle spinning (CPMAS) solid-state NMR spectra of organic solids. Spectra were obtained by impregnating substrates with a solution of the stable DNP polarizing agent TEKPol in tetrachloroethane. Tetrachloroethane is a non-solvent for the solids, and the unmodified substrates are then polarized through spin diffusion. High quality natural abundance (2)H CPMAS spectra of histidine hydrochloride monohydrate, glycylglycine and theophylline were acquired in less than 2h, providing direct access to hydrogen chemical shifts and quadrupolar couplings. The spectral resolution of the (2)H solid-state NMR spectra is comparable to that of (1)H spectra obtained with state of the art homonuclear decoupling techniques. PMID:26363582

  15. A human interactome in three quantitative dimensions organized by stoichiometries and abundances.

    PubMed

    Hein, Marco Y; Hubner, Nina C; Poser, Ina; Cox, Jürgen; Nagaraj, Nagarjuna; Toyoda, Yusuke; Gak, Igor A; Weisswange, Ina; Mansfeld, Jörg; Buchholz, Frank; Hyman, Anthony A; Mann, Matthias

    2015-10-22

    The organization of a cell emerges from the interactions in protein networks. The interactome is critically dependent on the strengths of interactions and the cellular abundances of the connected proteins, both of which span orders of magnitude. However, these aspects have not yet been analyzed globally. Here, we have generated a library of HeLa cell lines expressing 1,125 GFP-tagged proteins under near-endogenous control, which we used as input for a next-generation interaction survey. Using quantitative proteomics, we detect specific interactions, estimate interaction stoichiometries, and measure cellular abundances of interacting proteins. These three quantitative dimensions reveal that the protein network is dominated by weak, substoichiometric interactions that play a pivotal role in defining network topology. The minority of stable complexes can be identified by their unique stoichiometry signature. This study provides a rich interaction dataset connecting thousands of proteins and introduces a framework for quantitative network analysis. PMID:26496610

  16. Constraining the Abundances of Complex Organics in the Inner Regions of Solar-type Protostars

    NASA Astrophysics Data System (ADS)

    Taquet, Vianney; López-Sepulcre, Ana; Ceccarelli, Cecilia; Neri, Roberto; Kahane, Claudine; Charnley, Steven B.

    2015-05-01

    The high abundances of Complex Organic Molecules (COMs) with respect to methanol, the most abundant COM, detected toward low-mass protostars, tend to be underpredicted by astrochemical models. This discrepancy might come from the large beam of the single-dish telescopes, encompassing several components of the studied protostar, commonly used to detect COMs. To address this issue, we have carried out multi-line observations of methanol and several COMs toward the two low-mass protostars NGC 1333-IRAS 2A and -IRAS 4A with the Plateau de Bure interferometer at an angular resolution of 2″, resulting in the first multi-line detection of the O-bearing species glycolaldehyde and ethanol and of the N-bearing species ethyl cyanide toward low-mass protostars other than IRAS 16293. The high number of detected transitions from COMs (more than 40 methanol transitions for instance) allowed us to accurately derive the source size of their emission and the COM column densities. The COM abundances with respect to methanol derived toward IRAS 2A and IRAS 4A are slightly, but not substantitally, lower than those derived from previous single-dish observations. The COM abundance ratios do not vary significantly with the protostellar luminosity, over five orders of magnitude, implying that low-mass hot corinos are quite chemically rich as high-mass hot cores. Astrochemical models still underpredict the abundances of key COMs, such as methyl formate or di-methyl ether, suggesting that our understanding of their formation remains incomplete.

  17. Probabilisitc Geobiological Classification Using Elemental Abundance Distributions and Lossless Image Compression in Recent and Modern Organisms

    NASA Technical Reports Server (NTRS)

    Storrie-Lombardi, Michael C.; Hoover, Richard B.

    2005-01-01

    Last year we presented techniques for the detection of fossils during robotic missions to Mars using both structural and chemical signatures[Storrie-Lombardi and Hoover, 2004]. Analyses included lossless compression of photographic images to estimate the relative complexity of a putative fossil compared to the rock matrix [Corsetti and Storrie-Lombardi, 2003] and elemental abundance distributions to provide mineralogical classification of the rock matrix [Storrie-Lombardi and Fisk, 2004]. We presented a classification strategy employing two exploratory classification algorithms (Principal Component Analysis and Hierarchical Cluster Analysis) and non-linear stochastic neural network to produce a Bayesian estimate of classification accuracy. We now present an extension of our previous experiments exploring putative fossil forms morphologically resembling cyanobacteria discovered in the Orgueil meteorite. Elemental abundances (C6, N7, O8, Na11, Mg12, Ai13, Si14, P15, S16, Cl17, K19, Ca20, Fe26) obtained for both extant cyanobacteria and fossil trilobites produce signatures readily distinguishing them from meteorite targets. When compared to elemental abundance signatures for extant cyanobacteria Orgueil structures exhibit decreased abundances for C6, N7, Na11, All3, P15, Cl17, K19, Ca20 and increases in Mg12, S16, Fe26. Diatoms and silicified portions of cyanobacterial sheaths exhibiting high levels of silicon and correspondingly low levels of carbon cluster more closely with terrestrial fossils than with extant cyanobacteria. Compression indices verify that variations in random and redundant textural patterns between perceived forms and the background matrix contribute significantly to morphological visual identification. The results provide a quantitative probabilistic methodology for discriminating putatitive fossils from the surrounding rock matrix and &om extant organisms using both structural and chemical information. The techniques described appear applicable

  18. Determination of Natural 14C Abundances in Dissolved Organic Carbon in Organic-Rich Marine Sediment Porewaters by Thermal Sulfate Reduction

    NASA Astrophysics Data System (ADS)

    Johnson, L.; Komada, T.

    2010-12-01

    The abundances of natural 14C in dissolved organic carbon (DOC) in the marine environment hold clues regarding the processes that influence the biogeochemical cycling of this large carbon reservoir. At present, UV irradiation is the widely accepted method for oxidizing seawater DOC for determination of their 14C abundances. This technique yields precise and accurate values with low blanks, but it requires a dedicated vacuum line, and hence can be difficult to implement. As an alternative technique that can be conducted on a standard preparatory vacuum line, we modified and tested a thermal sulfate reduction method that was previously developed to determine δ13C values of marine DOC (Fry B. et al., 1996. Analysis of marine DOC using a dry combustion method. Mar. Chem., 54: 191-201.) to determine the 14C abundances of DOC in marine sediment porewaters. In this method, the sample is dried in a 100 ml round-bottom Pyrex flask in the presence of excess oxidant (K2SO4) and acid (H3PO4), and combusted at 550 deg.C. The combustion products are cryogenically processed to collect and quantify CO2 using standard procedures. Materials we have oxidized to date range from 6-24 ml in volume, and 95-1500 μgC in size. The oxidation efficiency of this method was tested by processing known amounts of reagent-grade dextrose and sucrose (as examples of labile organic matter), tannic acid and humic acid (as examples of complex natural organic matter), and porewater DOC extracted from organic-rich nearshore sediments. The carbon yields for all of these materials averaged 99±4% (n=18). The 14C abundances of standard materials IAEA C-6 and IAEA C-5 processed by this method using >1mgC aliquots were within error of certified values. The size and the isotopic value of the blank were determined by a standard dilution technique using IAEA C-6 and IAEA C-5 that ranged in size from 150 to 1500 μgC (n=4 and 2, respectively). This yielded a blank size of 6.7±0.7 μgC, and a blank isotopic

  19. Organic Cathode Materials for Rechargeable Batteries

    SciTech Connect

    Cao, Ruiguo; Qian, Jiangfeng; Zhang, Jiguang; Xu, Wu

    2015-06-28

    This chapter will primarily focus on the advances made in recent years and specify the development of organic electrode materials for their applications in rechargeable lithium batteries, sodium batteries and redox flow batteries. Four various organic cathode materials, including conjugated carbonyl compounds, conducting polymers, organosulfides and free radical polymers, are introduced in terms of their electrochemical performances in these three battery systems. Fundamental issues related to the synthesis-structure-activity correlations, involved work principles in energy storage systems, and capacity fading mechanisms are also discussed.

  20. Organic materials for fusion-reactor applications

    SciTech Connect

    Hurley, G.F.; Coltman, R.R. Jr.

    1983-09-01

    Organic materials requirements for fusion-reactor magnets are described with reference to the temperature, radiation, and electrical and mechanical stress environment expected in these magnets. A review is presented of the response to gamma-ray and neutron irradiation at low temperatures of candidate organic materials; i.e. laminates, thin films, and potting compounds. Lifetime-limiting features of this response as well as needed testing under magnet operating conditions not yet adequately investigated are identified and recomendations for future work are made.

  1. TREATMENT OF STORMWATER BY NATURAL ORGANIC MATERIALS

    EPA Science Inventory

    The overall objective of this study was to evaluate the feasibility of using low-cost natural filter materials for stormwater (SW) treatment. Generic mulch, pine bark mulch, and processed jute were evaluated for metal and organic pollutant removal from actual SW samples collected...

  2. Synthetic Organic Materials in Nuclear Powerplants

    NASA Technical Reports Server (NTRS)

    Bouquet, F. L.; Winslow, J. W.

    1985-01-01

    Report aids plant designers and qualification engineers in ensuring that organic materials in nuclear powerplants will perform satisfactorily in such safety-related equipment as insulation on motor windings, pump diaphragms, motor and pump lubricants, and pump seals and gaskets. Report provides information for service that may include both mild and harsh nuclear environments.

  3. ADSORPTION OF ORGANIC CATIONS TO NATURAL MATERIALS

    EPA Science Inventory

    The factors that control the extent of adsorption of amphiphilic organic cations on environmental and pristine surfaces have been studied. he sorbents were kaolinite, montmorillonite, two aquifer materials, and a soil; solutions contained various concentrations of NaCl and CaC12,...

  4. ADSORPTION OF ORGANIC CATIONS TO NATURAL MATERIALS

    EPA Science Inventory

    The factors that control the extent of adsorption of amphiphilic organic cations on environmental and pristine surfaces have been studied. The sorbents were kaolinite, montmorillonite, two aquifer materials, and a soil; solutions contained various concentrations of NaCl and CaCl,...

  5. The Mars Science Laboratory Organic Check Material

    NASA Technical Reports Server (NTRS)

    Conrad, Pamela G.; Eigenbrode, J. E.; Mogensen, C. T.; VonderHeydt, M. O.; Glavin, D. P.; Mahaffy, P. M.; Johnson, J. A.

    2011-01-01

    The Organic Check Material (OCM) has been developed for use on the Mars Science Laboratory mission to serve as a sample standard for verification of organic cleanliness and characterization of potential sample alteration as a function of the sample acquisition and portioning process on the Curiosity rover. OCM samples will be acquired using the same procedures for drilling, portioning and delivery as are used to study martian samples with The Sample Analysis at Mars (SAM) instrument suite during MSL surface operations. Because the SAM suite is highly sensitive to organic molecules, the mission can better verify the cleanliness of Curiosity's sample acquisition hardware if a known material can be processed through SAM and compared with the results obtained from martian samples.

  6. Shock-induced chemistry in organic materials

    SciTech Connect

    Dattelbaum, Dana M; Sheffield, Steve; Engelke, Ray; Manner, Virginia; Chellappa, Raja; Yoo, Choong - Shik

    2011-01-20

    The combined 'extreme' environments of high pressure, temperature, and strain rates, encountered under shock loading, offer enormous potential for the discovery of new paradigms in chemical reactivity not possible under more benign conditions. All organic materials are expected to react under these conditions, yet we currently understand very little about the first bond-breaking steps behind the shock front, such as in the shock initiation of explosives, or shock-induced reactivity of other relevant materials. Here, I will present recent experimental results of shock-induced chemistry in a variety of organic materials under sustained shock conditions. A comparison between the reactivity of different structures is given, and a perspective on the kinetics of reaction completion under shock drives.

  7. Predators alter community organization of coral reef cryptofauna and reduce abundance of coral mutualists

    NASA Astrophysics Data System (ADS)

    Stier, A. C.; Leray, M.

    2014-03-01

    Coral reefs are the most diverse marine systems in the world, yet our understanding of the processes that maintain such extraordinary diversity remains limited and taxonomically biased toward the most conspicuous species. Cryptofauna that live deeply embedded within the interstitial spaces of coral reefs make up the majority of reef diversity, and many of these species provide important protective services to their coral hosts. However, we know very little about the processes governing the diversity and composition of these less conspicuous but functionally important species. Here, we experimentally quantify the role of predation in driving the community organization of small fishes and decapods that live embedded within Pocillopora eydouxi, a structurally complex, reef-building coral found widely across the Indo-Pacific. We use surveys to describe the natural distribution of predators, and then, factorially manipulate two focal predator species to quantify the independent and combined effects of predator density and identity on P. eydouxi-dwelling cryptofauna. Predators reduced abundance (34 %), species richness (20 %), and modified species composition. Rarefaction revealed that observed reductions in species richness were primarily driven by changes in abundance. Additionally, the two predator species uniquely affected the beta diversity and composition of the prey assemblage. Predators reduced the abundance and modified the composition of a number of mutualist fishes and decapods, whose benefit to the coral is known to be both diversity- and density-dependent. We predict that the density and identity of predators present within P. eydouxi may substantially alter coral performance in the face of an increased frequency and intensity of natural and anthropogenic stressors.

  8. Targeted Access to the Genomes of Low Abundance Organisms in Complex Microbial Communities

    SciTech Connect

    Podar, Mircea; Abulencia, Carl; Walcher, Marion; Hutchinson, Don; Zengler, Karsten; Garcia, Joseph; Holland, Trevin; Cotton, Dave; Hauser, Loren John; Keller, Martin

    2007-01-01

    Current metagenomic approaches to the study of complex microbial consortia provide a glimpse into the community metabolism, and occasionally allow genomic assemblies for the most abundant organisms. However, little information is gained for the members of the community present at low frequency, especially those representing yet uncultured taxa-which includes the bulk of the diversity present in most environments. Here we used phylogenetically directed cell separation by fluorescence in situ hybridization and flow cytometry, followed by amplification and sequencing of a fraction of the genomic DNA of several bacterial cells that belong to the TM7 phylum. Partial genomic assembly allowed, for the first time, a look into the evolution and potential metabolism of a soil representative from this group of organisms for which there are no species in stable laboratory cultures. Genomic reconstruction from targeted cells of uncultured organisms directly isolated from the environment represents a powerful approach to access any specific members of a community and an alternative way to assess the community metabolic potential.

  9. Organic materials with nonlinear optical properties

    DOEpatents

    Stupp, S.I.; Son, S.; Lin, H.C.

    1995-05-02

    The present invention is directed to organic materials that have the ability to double or triple the frequency of light that is directed through the materials. Particularly, the present invention is directed to the compound 4-[4-(2R)-2-cyano-7-(4{prime}-pentyloxy-4-biphenylcarbonyloxy)phenylheptylidenephenylcarbonyloxy]benzaldehyde, which can double the frequency of light that is directed through the compound. The invention is also directed to the compound (12-hydroxy-5,7-dodecadiynyl)-4{prime}-[(4{prime}-pentyloxy-4-biphenyl)carbonyloxy]-4-biphenylcarboxylate, and its polymeric form. The polymeric form can triple the frequency of light directed through it. 4 figs.

  10. Optical mirror coated with organic superconducting material

    NASA Astrophysics Data System (ADS)

    Lake, John A.; Heath, William B.

    1988-08-01

    An optical mirror has enhanced reflectivity and reduced thermal distortions when it is composed of a substrate coated with a reflective coating made of an organic superconducting material. The substrate is best constructed of materials which have the most favorable thermal expansion and thermal conduction characteristics at temperatures near 0 K. such as: silicon, diamond, copper, and sapphire. The reflective coating is only a few microns thick and composed of organometallic compounds and is cooled to superconducting or cryogenic temperatures of less than 100 K.

  11. Physics and Materials Issues of Organic Photovoltaics

    NASA Astrophysics Data System (ADS)

    Scully, Shawn R.; McGehee, Michael D.

    Organic materials hold promise for use in photovoltaic (PV) devices because of their potential to reduce the cost of electricity per kWh ultimately to levels below that of electricity produced by coal-fired power plants. Deposition of organics by techniques such as screen printing, doctor blading, inkjet printing, spray deposition, and thermal evaporation lends itself to incorporation in high-throughput low-cost roll-to-roll coating systems. These are low-temperature deposition techniques which allow the organics to be deposited on plastic substrates such that flexible devices can easily be made. In addition to the inherent economics of high-throughput manufacturing, lightweight and flexibility are qualities claimed to offer a simple way to reduce the price of PV panels by reducing installation costs. Flexible PVs also open niche markets like portable power generation and aesthetic-PV in building design.

  12. Acetylene-Based Materials in Organic Photovoltaics

    PubMed Central

    Silvestri, Fabio; Marrocchi, Assunta

    2010-01-01

    Fossil fuel alternatives, such as solar energy, are moving to the forefront in a variety of research fields. Organic photovoltaic systems hold the promise of a lightweight, flexible, cost-effective solar energy conversion platform, which could benefit from simple solution-processing of the active layer. The discovery of semiconductive polyacetylene by Heeger et al. in the late 1970s was a milestone towards the use of organic materials in electronics; the development of efficient protocols for the palladium catalyzed alkynylation reactions and the new conception of steric and conformational advantages of acetylenes have been recently focused the attention on conjugated triple-bond containing systems as a promising class of semiconductors for OPVs applications. We review here the most important and representative (poly)arylacetylenes that have been used in the field. A general introduction to (poly)arylacetylenes, and the most common synthetic approaches directed toward making these materials will be firstly given. After a brief discussion on working principles and critical parameters of OPVs, we will focus on molecular arylacetylenes, (co)polymers containing triple bonds, and metallopolyyne polymers as p-type semiconductor materials. The last section will deal with hybrids in which oligomeric/polymeric structures incorporating acetylenic linkages such as phenylene ethynylenes have been attached onto C60, and their use as the active materials in photovoltaic devices. PMID:20480031

  13. Effects of multiple levels of social organization on survival and abundance.

    PubMed

    Ward, Eric J; Semmens, Brice X; Holmes, Elizabeth E; Balcomb Iii, Ken C

    2011-04-01

    Identifying how social organization shapes individual behavior, survival, and fecundity of animals that live in groups can inform conservation efforts and improve forecasts of population abundance, even when the mechanism responsible for group-level differences is unknown. We constructed a hierarchical Bayesian model to quantify the relative variability in survival rates among different levels of social organization (matrilines and pods) of an endangered population of killer whales (Orcinus orca). Individual killer whales often participate in group activities such as prey sharing and cooperative hunting. The estimated age-specific survival probabilities and survivorship curves differed considerably among pods and to a lesser extent among matrilines (within pods). Across all pods, males had lower life expectancy than females. Differences in survival between pods may be caused by a combination of factors that vary across the population's range, including reduced prey availability, contaminants in prey, and human activity. Our modeling approach could be applied to demographic rates for other species and for parameters other than survival, including reproduction, prey selection, movement, and detection probabilities. PMID:21054527

  14. From molecular design and materials construction to organic nanophotonic devices.

    PubMed

    Zhang, Chuang; Yan, Yongli; Zhao, Yong Sheng; Yao, Jiannian

    2014-12-16

    CONSPECTUS: Nanophotonics has recently received broad research interest, since it may provide an alternative opportunity to overcome the fundamental limitations in electronic circuits. Diverse optical materials down to the wavelength scale are required to develop nanophotonic devices, including functional components for light emission, transmission, and detection. During the past decade, the chemists have made their own contributions to this interdisciplinary field, especially from the controlled fabrication of nanophotonic molecules and materials. In this context, organic micro- or nanocrystals have been developed as a very promising kind of building block in the construction of novel units for integrated nanophotonics, mainly due to the great versatility in organic molecular structures and their flexibility for the subsequent processing. Following the pioneering works on organic nanolasers and optical waveguides, the organic nanophotonic materials and devices have attracted increasing interest and developed rapidly during the past few years. In this Account, we review our research on the photonic performance of molecular micro- or nanostructures and the latest breakthroughs toward organic nanophotonic devices. Overall, the versatile features of organic materials are highlighted, because they brings tunable optical properties based on molecular design, size-dependent light confinement in low-dimensional structures, and various device geometries for nanophotonic integration. The molecular diversity enables abundant optical transitions in conjugated π-electron systems, and thus brings specific photonic functions into molecular aggregates. The morphology of these micro- or nanostructures can be further controlled based on the weak intermolecular interactions during molecular assembly process, making the aggregates show photon confinement or light guiding properties as nanophotonic materials. By adoption of some active processes in the composite of two or more

  15. Photonic crystals with active organic materials

    NASA Astrophysics Data System (ADS)

    Wu, Yeheng

    The concept of photonic crystals, which involves periodically arranged dielectrics that form a new type of material having novel photonic properties, was first proposed about two decades ago. Since then, a number of applications in photonic technology have been explored. Specifically, organic and hybrid photonic crystals are promising because of the unique advantages of the organic materials. A one-dimensional (1D) photonic crystal (multilayer) has high reflectance across a certain wavelength range. We report on studies of 1D multilayer polymer films that were fabricated using spin-coating, free film stacking, and co-extrusion techniques. For example, a stack fabricated by placing a laser dye-doped gain medium between two multilayer reflecting polymer films forms a micro-resonator laser or distributed Bragg laser. The resulting laser system is made entirely of plastic and is only several tens of micrometers in thickness. When the gain, a dye-doped medium, comprises one type of a two-type multilayer film, it results a laser exhibiting distributed feedback. At the edge of the photonic band, the group velocity becomes small and the density of photon states becomes high, which leads to laser emission. Such distributed feedback lasers were fabricated using the co-extrusion technique. The refractive indices and the photonic lattice determine the photonic band gap, which can be tuned by changing these parameters. Materials with Kerr nonlinearity exhibit a change in refractive index depending on the incident intensity of the light. To demonstrate such switching, electrochemical etching techniques on silicon wafers were used to form two-dimensional (2D) photonic crystals. By incorporating the nonlinear organic material into the 2D structure, we have made all-optical switches. The reflection of a beam from the 2D photonic crystal can be controlled by another beam because it induces a refractive index change in the active material by altering the reflection band. A mid

  16. Processes and Materials for Organic Photovoltaics

    NASA Astrophysics Data System (ADS)

    Cox, Marshall

    The field of organic photovoltaics is driven by the desire for better and cheaper solar cells. While showing much promise, current generations of organic photovoltaic (OPV) devices do not exhibit properties that are suited for wide scale commercialization. While much research has been dedicated towards this goal, more yet needs to be done before it can be clear whether this is an achievable goal. This thesis describes new materials investigations for higher efficiency better stability organic photovoltaics, as well as new processes that broaden the application and fabrication space for these devices. The application of electro-polymerization, a deposition process, towards organic thin-film fabrication is discussed. This novel process for OPVs is followed by an analysis of new and interesting materials for OPV devices, including a higher efficiency hole-transporting material, and two hole-transporting molecules that exhibit self-assembly during OPV fabrication. The results of these investigations indicate the possibility for increased fabrication freedom and control, molecular species design that could allow higher efficiency devices, as well as indications of the role that molecular interactions in OPV heterojunctions play. In addition, the possibilities of integrating graphene, the two-dimensional form of carbon, into OPV architectures is discussed. A new process for graphene transfer that allows the integration of graphene into chemically and physically more fragile systems including those composed of small molecule semiconductors is described and experimentally verified. Graphene is then integrated as a cathode in OPVs, and a modeling and experimental investigation is performed to evaluate the potential for integrating graphene as a recombination layer in tandem OPVs. Based on this investigation, the integration of graphene into tandem OPVs could enable higher efficiency devices and significantly broadened architectural freedom for tandem fabrication.

  17. Microporous Metal Organic Materials for Hydrogen Storage

    SciTech Connect

    S. G. Sankar; Jing Li; Karl Johnson

    2008-11-30

    We have examined a number of Metal Organic Framework Materials for their potential in hydrogen storage applications. Results obtained in this study may, in general, be summarized as follows: (1) We have identified a new family of porous metal organic framework materials with the compositions M (bdc) (ted){sub 0.5}, {l_brace}M = Zn or Co, bdc = biphenyl dicarboxylate and ted = triethylene diamine{r_brace} that adsorb large quantities of hydrogen ({approx}4.6 wt%) at 77 K and a hydrogen pressure of 50 atm. The modeling performed on these materials agree reasonably well with the experimental results. (2) In some instances, such as in Y{sub 2}(sdba){sub 3}, even though the modeling predicted the possibility of hydrogen adsorption (although only small quantities, {approx}1.2 wt%, 77 K, 50 atm. hydrogen), our experiments indicate that the sample does not adsorb any hydrogen. This may be related to the fact that the pores are extremely small or may be attributed to the lack of proper activation process. (3) Some samples such as Zn (tbip) (tbip = 5-tert butyl isophthalate) exhibit hysteresis characteristics in hydrogen sorption between adsorption and desorption runs. Modeling studies on this sample show good agreement with the desorption behavior. It is necessary to conduct additional studies to fully understand this behavior. (4) Molecular simulations have demonstrated the need to enhance the solid-fluid potential of interaction in order to achieve much higher adsorption amounts at room temperature. We speculate that this may be accomplished through incorporation of light transition metals, such as titanium and scandium, into the metal organic framework materials.

  18. Adaptation of an abundant Roseobacter RCA organism to pelagic systems revealed by genomic and transcriptomic analyses.

    PubMed

    Voget, Sonja; Wemheuer, Bernd; Brinkhoff, Thorsten; Vollmers, John; Dietrich, Sascha; Giebel, Helge-Ansgar; Beardsley, Christine; Sardemann, Carla; Bakenhus, Insa; Billerbeck, Sara; Daniel, Rolf; Simon, Meinhard

    2015-02-01

    The RCA (Roseobacter clade affiliated) cluster, with an internal 16S rRNA gene sequence similarity of >98%, is the largest cluster of the marine Roseobacter clade and most abundant in temperate to (sub)polar oceans, constituting up to 35% of total bacterioplankton. The genome analysis of the first described species of the RCA cluster, Planktomarina temperata RCA23, revealed that this phylogenetic lineage is deeply branching within the Roseobacter clade. It shares not >65.7% of homologous genes with any other organism of this clade. The genome is the smallest of all closed genomes of the Roseobacter clade, exhibits various features of genome streamlining and encompasses genes for aerobic anoxygenic photosynthesis (AAP) and CO oxidation. In order to assess the biogeochemical significance of the RCA cluster we investigated a phytoplankton spring bloom in the North Sea. This cluster constituted 5.1% of the total, but 10-31% (mean 18.5%) of the active bacterioplankton. A metatranscriptomic analysis showed that the genome of P. temperata RCA23 was transcribed to 94% in the bloom with some variations during day and night. The genome of P. temperata RCA23 was also retrieved to 84% from metagenomic data sets from a Norwegian fjord and to 82% from stations of the Global Ocean Sampling expedition in the northwestern Atlantic. In this region, up to 6.5% of the total reads mapped on the genome of P. temperata RCA23. This abundant taxon appears to be a major player in ocean biogeochemistry. PMID:25083934

  19. Composition of estuarine colloidal material: organic components

    USGS Publications Warehouse

    Sigleo, A.C.; Hoering, T.C.; Helz, G.R.

    1982-01-01

    Colloidal material in the size range 1.2 nm to 0.4 ??m was isolated by ultrafiltration from Chesapeake Bay and Patuxent River waters (U.S.A.). Temperature controlled, stepwise pyrolysis of the freeze-dried material, followed by gas chromatographic-mass spectrometric analyses of the volatile products indicates that the primary organic components of this polymer are carbohydrates and peptides. The major pyrolysis products at the 450??C step are acetic acid, furaldehydes, furoic acid, furanmethanol, diones and lactones characteristic of carbohydrate thermal decomposition. Pyrroles, pyridines, amides and indole (protein derivatives) become more prevalent and dominate the product yield at the 600??C pyrolysis step. Olefins and saturated hydrocarbons, originating from fatty acids, are present only in minor amounts. These results are consistent with the composition of Chesapeake phytoplankton (approximately 50% protein, 30% carbohydrate, 10% lipid and 10% nucleotides by dry weight). The pyrolysis of a cultured phytoplankton and natural particulate samples produced similar oxygen and nitrogencontaining compounds, although the proportions of some components differ relative to the colloidal fraction. There were no lignin derivatives indicative of terrestrial plant detritus in any of these samples. The data suggest that aquatic microorganisms, rather than terrestrial plants, are the dominant source of colloidal organic material in these river and estuarine surface waters. ?? 1982.

  20. Seasonal abundance of organic molecular markers in urban particulate matter from Philadelphia, PA

    NASA Astrophysics Data System (ADS)

    Li, Min; McDow, Stephen R.; Tollerud, David J.; Mazurek, Monica A.

    Organic molecular markers were measured in airborne particulate matter (PM10) from the City of Philadelphia North Broad Street air quality monitoring site to identify the seasonal abundance of key tracer compounds together with their dominant sources. Daily PM10 samples were collected seasonally in 2000 for four 2-week periods (January, April, August, and October). The North Broad Street site is within a heavily populated location in Philadelphia, PA. A suite of 52 individual organic marker compounds was monitored in the PM10 samples. Molecular markers, homologous compound series, and nonpolar and polar organic compounds were detected at ng m -3 ambient concentrations using gas chromatography/ion trap mass spectrometry (GC/IT MS). Organic diacids (C 3-C 9) and monoacids (C 10-C 30) had seasonal mass concentrations ranging from 91.0 (winter) to 261.8 ng m -3 (summer). Total n-alkanes (C 25-C 33) ranged from 25.9 (spring) to 49.5 ng m -3 (fall), total PAHs from 2.1 ng m -3 (summer) to 4.1 ng m -3 (winter), and total hopanes ranged from 4.0 ng m -3 (winter) to 7.4 ng m -3 (fall). The molecular marker ambient mass concentrations were normalized by the annual average mass of PM10 elemental carbon (EC) for the central Philadelphia area. The ambient mass concentrations to EC and OC ratios ranged from 2.6×10 -3 for total PAHs to EC to 115.3×10 -3 for total n-alkanoic acids to EC, 0.5×10 -3 for total PAHs to OC to 23.8×10 -3 for total n-alkanoic acids to OC. Ambient concentrations of individual markers are similar to other reported levels for metropolitan Los Angeles, CA and Atlanta, GA. Seasonal and daily variations of marker compounds are consistent with motor vehicle exhaust, particularly in winter. Summer concentration patterns indicate the importance of secondary organic aerosol to the PM10 ambient mass.

  1. Biomimicry in metal-organic materials

    SciTech Connect

    Zhang, MW; Gu, ZY; Bosch, M; Perry, Z; Zhou, HC

    2015-06-15

    Nature has evolved a great number of biological molecules which serve as excellent constructional or functional units for metal-organic materials (MOMs). Even though the study of biomimetic MOMs is still at its embryonic stage, considerable progress has been made in the past few years. In this critical review, we will highlight the recent advances in the design, development and application of biomimetic MOMs, and illustrate how the incorporation of biological components into MOMs could further enrich their structural and functional diversity. More importantly, this review will provide a systematic overview of different methods for rational design of MOMs with biomimetic features. Published by Elsevier B.V.

  2. Organic material: Asteroids, meteorites, and planetary satellites

    NASA Technical Reports Server (NTRS)

    Cruikshank, Dale P.; Kerridge, John F.

    1992-01-01

    Telescopic observations in in situ spacecraft investigations over the last two decades have shown that many planetary satellites, asteroids, and comets have surfaces containing very dark material that is either neutral (black) or red in color. Although comets are not the focus of this paper, the possible relationship of comets to asteroids, meteorites, and interplanetary dust is briefly discussed in the context of their dark-matter component. The following topics are discussed with respect to their organic content: carbonaceous chondrites; asteroids; low-albedo planetary satellites; and Pluto, Charon, and Triton. Laboratory studies and a summary are also presented.

  3. Supramolecular materials: Self-organized nanostructures

    SciTech Connect

    Stupp, S.I.; LeBonheur, V.; Walker, K.

    1997-04-18

    Miniaturized triblock copolymers have been found to self-assemble into nanostructures that are highly regular in size and shape. Mushroom-shaped supramolecular structures of about 200 kilodaltons form by crystallization of the chemically identical blocks and self-organize into films containing 100 or more layers stacked in a polar arrangement. The polar supramolecular material exhibits spontaneous second-harmonic generation from infrared to green photons and has an adhesive tape-like character with nonadhesive-hydrophobic and hydrophilic-sticky opposite surfaces. The films also have reasonable shear strength and adhere tenaciously to glass surfaces on one side only. The regular and finite size of the supramolecular units is believed to be mediated by repulsive forces among some of the segments in the triblock molecules. A large diversity of multifunctional materials could be formed from regular supramolecular units weighing hundreds of kilodaltons. 21 refs., 10 figs.

  4. Crystalline Organic Cavitands As Microcavity Materials

    NASA Astrophysics Data System (ADS)

    Kane, Christopher Michael

    There has been much interest in inefficiently packed molecular materials and their applications in gas storage, separations, catalysis, etc. Such known materials include metal-organic frameworks (MOFs), polymers of intrinsic microporosity (PIMs), container molecule materials, etc. One way to design inefficiently packed materials is to construct them from compounds that are incapable of close-packing, that is rigid scaffolds with enforced cavities that cannot be filled by self-packing. Cavitand molecules, tetrameric macrocycles derived from calix[4]resorcinarene derivatives, are well known for their propensity to form crystalline inclusion compounds with small molecules; for example, of the 169 examples of calix[4]resorcinarene scaffolds found in the Cambridge Structural Database (CSD), no guest-free forms exist. The guest-free forms of various cavitands, synthesized by literature methods, have been obtained as single crystals by sublimation. Gas inclusion compounds of these cavitands have also been isolated and studied by single crystal x-ray diffraction, thermogravimetric analysis, and 1 H NMR. Furthermore, some cavitand derivatives have shown promise as media for industrial separations (Kr vs. Xe, MeCl vs. DME, Propene vs. Propane).

  5. Computer simulation of metal-organic materials

    NASA Astrophysics Data System (ADS)

    Stern, Abraham C.

    Computer simulations of metal-organic frameworks are conducted to both investigate the mechanism of hydrogen sorption and to elucidate a detailed, molecular-level understanding of the physical interactions that can lead to successful material design strategies. To this end, important intermolecular interactions are identified and individually parameterized to yield a highly accurate representation of the potential energy landscape. Polarization, one such interaction found to play a significant role in H 2 sorption, is included explicitly for the first time in simulations of metal-organic frameworks. Permanent electrostatics are usually accounted for by means of an approximate fit to model compounds. The application of this method to simulations involving metal-organic frameworks introduces several substantial problems that are characterized in this work. To circumvent this, a method is developed and tested in which atomic point partial charges are computed more directly, fit to the fully periodic electrostatic potential. In this manner, long-range electrostatics are explicitly accounted for via Ewald summation. Grand canonical Monte Carlo simulations are conducted employing the force field parameterization developed here. Several of the major findings of this work are: Polarization is found to play a critical role in determining the overall structure of H2 sorbed in metal-organic frameworks, although not always the determining factor in uptake. The parameterization of atomic point charges by means of a fit to the periodic electrostatic potential is a robust, efficient method and consistently results in a reliable description of Coulombic interactions without introducing ambiguity associated with other procedures. After careful development of both hydrogen and framework potential energy functions, quantitatively accurate results have been obtained. Such predictive accuracy will aid greatly in the rational, iterative design cycle between experimental and theoretical

  6. Characterization of a flood-associated deposit on the Waipaoa River shelf using radioisotopes and terrigenous organic matter abundance and composition

    NASA Astrophysics Data System (ADS)

    Kniskern, Tara A.; Mitra, Siddhartha; Orpin, Alan R.; Harris, Courtney K.; Walsh, J. P.; Corbett, D. R.

    2014-09-01

    An ephemeral oceanic-flood deposit adjacent to a well-studied small mountainous river (SMR), the Waipaoa River in northeastern New Zealand, was characterized using multiple proxies, including radioisotopes (234Th, 7Be, and 210Pb), bulk organic carbon abundance and isotopic signature (%OC, δ13C), as well as a biomarker of terrigenous organic matter (lignin). Field sampling was conducted within two weeks after a 1-in-8 year flood that occurred between January 30 and February 6, 2010. Geochemical analyses indicated that initial deposition of fresh riverine material extended alongshore to the north and south from the river mouth. A comparison of prior- and post-flood 7Be inventories revealed that flood sediments were widely dispersed between 20 and 70 m water depth, accounting for 50-80% of the estimated flood load. Surface (0-2 cm) isotopic carbon values increased with distance from Poverty Bay, positively correlating with total 210Pb activities, potentially reflecting increasing marine influence with water depth. Abundances of sedimentary organic carbon (OC) were 0.18-0.76% dry weight, and the total nitrogen varied from 0.02 to 0.13%. Stable isotope signatures of carbon (δ13COC), nitrogen (δ15N), and lignin abundances (λ6) throughout the study area ranged from -23.6 to -27.7‰, 1.9 to 5.3‰, and 0.93 to 9.0 mg 100 mg OC-1, respectively. The spatial distribution pattern of terrigenous organic matter (OM) abundance and interclass ratios (indicative of freshness of organic matter) varied along and across-shelf. Lignin abundances were high and interclass ratios were low in the southern depocenter and inner shelf areas, suggesting that this zone had recently received vascular-plant enriched OM, minimally altered by shelf-bed mixing processes. In contrast, sediments in the northern depocenter and outer shelf also contained elevated amounts of terrigenous sedimentary OM, but this material was generally lower in lignin abundance and had higher interclass ratios

  7. Characterization of Antibiotic Resistance Gene Abundance and Microbiota Composition in Feces of Organic and Conventional Pigs from Four EU Countries.

    PubMed

    Gerzova, Lenka; Babak, Vladimir; Sedlar, Karel; Faldynova, Marcela; Videnska, Petra; Cejkova, Darina; Jensen, Annette Nygaard; Denis, Martine; Kerouanton, Annaelle; Ricci, Antonia; Cibin, Veronica; Österberg, Julia; Rychlik, Ivan

    2015-01-01

    One of the recent trends in animal production is the revival of interest in organic farming. The increased consumer interest in organic animal farming is mainly due to concerns about animal welfare and the use of antibiotics in conventional farming. On the other hand, providing animals with a more natural lifestyle implies their increased exposure to environmental sources of different microorganisms including pathogens. To address these concerns, we determined the abundance of antibiotic resistance and diversity within fecal microbiota in pigs kept under conventional and organic farming systems in Sweden, Denmark, France and Italy. The abundance of sul1, sul2, strA, tet(A), tet(B) and cat antibiotic resistance genes was determined in 468 samples by real-time PCR and the fecal microbiota diversity was characterized in 48 selected samples by pyrosequencing of V3/V4 regions of 16S rRNA. Contrary to our expectations, there were no extensive differences between the abundance of tested antibiotic resistance genes in microbiota originating from organic or conventionally housed pigs within individual countries. There were also no differences in the microbiota composition of organic and conventional pigs. The only significant difference was the difference in the abundance of antibiotic resistance genes in the samples from different countries. Fecal microbiota in the samples originating from southern European countries (Italy, France) exhibited significantly higher antibiotic resistance gene abundance than those from northern parts of Europe (Denmark, Sweden). Therefore, the geographical location of the herd influenced the antibiotic resistance in the fecal microbiota more than farm's status as organic or conventional. PMID:26218075

  8. Novel High Efficient Organic Photovoltaic Materials

    NASA Technical Reports Server (NTRS)

    Sun, Sam; Haliburton, James; Wang, Yi-Qing; Fan, Zhen; Taft, Charles; Maaref, Shahin; Bailey, Sheila (Technical Monitor)

    2003-01-01

    Solar energy is a renewable, nonpolluting, and most abundant energy source for human exploration of a remote site or outer space. In order to generate appreciable electrical power in space or on the earth, it is necessary to collect sunlight from large areas and with high efficiency due to the low density of sunlight. Future organic or polymer (plastic) solar cells appear very attractive due to their unique features such as light weight, flexible shape, tunability of energy band-gaps via versatile molecular or supramolecular design, synthesis, processing and device fabrication schemes, and much lower cost on large scale industrial production. It has been predicted that supramolecular and nano-phase separated block copolymer systems containing electron rich donor blocks and electron deficient acceptor blocks may facilitate the charge carrier separation and migration due to improved electronic ultrastructure and morphology in comparison to polymer composite system. This presentation will describe our recent progress in the design, synthesis and characterization of a novel block copolymer system containing donor and acceptor blocks covalently attached. Specifically, the donor block contains an electron donating alkyloxy derivatized polyphenylenevinylene (RO-PPV), the acceptor block contains an electron withdrawing alkyl-sulfone derivatized polyphenylenevinylene (SF-PPV). The key synthetic strategy includes the synthesis of each individual block first, then couple the blocks together. While the donor block has a strong PL emission at around 560 nm, and acceptor block has a strong PL emission at around 520 nm, the PL emissions of final block copolymers are severely quenched. This verifies the expected electron transfer and charge separation due to interfaces of donor and acceptor nano phase separated blocks. The system therefore has potential for variety light harvesting applications, including high efficient photovoltaic applications.

  9. Preface: Thin films of molecular organic materials

    NASA Astrophysics Data System (ADS)

    Fraxedas, J.

    2008-03-01

    This special issue is devoted to thin films of molecular organic materials and its aim is to assemble numerous different aspects of this topic in order to reach a wide scientific audience. Under the term 'thin films', structures with thicknesses spanning from one monolayer or less up to several micrometers are included. In order to narrow down this relaxed definition (how thin is thin?) I suggest joining the stream that makes a distinction according to the length scale involved, separating nanometer-thick films from micrometer-thick films. While the physical properties of micrometer-thick films tend to mimic those of bulk materials, in the low nanometer regime new structures (e.g., crystallographic and substrate-induced phases) and properties are found. However, one has to bear in mind that some properties of micrometer-thick films are really confined to the film/substrate interface (e.g. charge injection), and are thus of nanometer nature. Supported in this dimensionality framework, this issue covers the most ideal and model 0D case, a single molecule on a surface, through to the more application-oriented 3D case, placing special emphasis on the fascinating 2D domain that is monolayer assembly. Thus, many aspects will be reviewed, such as single molecules, self-organization, monolayer regime, chirality, growth, physical properties and applications. This issue has been intentionally restricted to small molecules, thus leaving out polymers and biomolecules, because for small molecules it is easier to establish structure--property relationships. Traditionally, the preparation of thin films of molecular organic materials has been considered as a secondary, lower-ranked part of the more general field of this class of materials. The coating of diverse surfaces such as silicon, inorganic and organic single crystals, chemically modified substrates, polymers, etc., with interesting molecules was driven by the potential applications of such molecular materials

  10. Quantifying water diffusion in secondary organic material

    NASA Astrophysics Data System (ADS)

    Price, Hannah; Murray, Benjamin; Mattsson, Johan; O'Sullivan, Daniel; Wilson, Theodore; Zhang, Yue; Martin, Scot

    2014-05-01

    Recent research suggests that some secondary organic aerosol (SOA) is highly viscous under certain atmospheric conditions. This may have important consequences for equilibration timescales, SOA growth, heterogeneous chemistry and ice nucleation. In order to quantify these effects, knowledge of the diffusion coefficients of relevant gas species within aerosol particles is vital. In this work, a Raman isotope tracer method is used to quantify water diffusion coefficients over a range of atmospherically relevant humidity and temperature conditions. D2O is observed as it diffuses from the gas phase into a disk of aqueous solution, without the disk changing in size or viscosity. An analytical solution of Fick's second law is then used with a fitting procedure to determine water diffusion coefficients in reference materials for method validation. The technique is then extended to compounds of atmospheric relevance and α-pinene secondary organic material. We produce water diffusion coefficients from 20 to 80 % RH at 23.5° C for sucrose, levoglucosan, M5AS and MgSO4. For levoglucosan we show that under conditions where a particle bounces, water diffusion in aqueous solutions can be fast (a fraction of a second for a 100 nm radius). For sucrose solutions, we also show that the Stokes-Einstein relation breaks down at high viscosity and cannot be used to predict water diffusion timescales with accuracy. In addition, we also quantify water diffusion coefficients in α-pinene SOM from 20-80% RH and over temperatures from 6 to -30° C. Our results suggest that, at 6° C, water diffusion in α-pinene SOA is not kinetically limited on the second timescale, even at 20% RH. As temperatures decrease, however, diffusion slows and may become an increasingly limiting factor for atmospheric processes. A parameterization for the diffusion coefficient of water in α-pinene secondary organic material, as a function of relative humidity and temperature, is presented. The implications for

  11. Inorganic-organic materials incorporating alumoxane nanoparticles

    NASA Astrophysics Data System (ADS)

    Vogelson, Cullen Taylor

    Chemically functionalized alumina nanoparticles (carboxylate-alumoxanes) are used as the inorganic component of a new class of inorganic-organic material. Lysine- or para-hydroxybenzoic acid-derivatized alumoxanes are prepared from the reaction of boehmite, [Al(O)(OH)]n, with the appropriate carboxylic acid. The peripheral hydroxides and amines of these alumoxanes react directly with DER 332 epoxide to form a hybrid material, or in the presence of a resin and hardener system, to form a composite material. Solid state NMR spectroscopy demonstrates that the alumoxanes are chemically bound to the resin matrix. The properties and cure times of the alumoxane materials are distinct from both the pure resins and from a physical blend of the resins with traditional fillers. A significant increase in thermal stability and tensile strength is observed for the resin systems. In order to produce molecular coupling layers, epoxides cross-linked with self-assembled monolayers (SAMs) grown on the native oxide of aluminum thin films on silicon substrates have been investigated. Specifically, SAMs have been formed by the attachment of different carboxylic acids. In order to investigate the cross-linking reaction between carboxylate monolayers and an epoxide, grown monolayers were reacted with a mono-epoxy resin. In addition to these surface materials, aluminum oxide surfaces supporting carboxylate monolayers were reacted in pairs with DER 332 to form a structural adhesive. These materials have been characterized variously by SEM, AFM, XPS, EDX, and contact angle measurements. The particle size dependence on pH of a series of alumoxanes was investigated. For each of the alumoxanes, PCS particle size measurements were obtained as a function of pH. In all cases, particle size control was afforded by variations in pH. Finally, crystal structures of several model compounds were determined by X-ray crystallography, and shown to form either sheets of dimers or tetrameric units. Through a

  12. The abundance and organization of polypeptides associated with antigens of the Rh blood group system.

    PubMed

    Gardner, B; Anstee, D J; Mawby, W J; Tanner, M J; von dem Borne, A E

    1991-06-01

    Twelve murine monoclonal antibodies, which react with human red cells of common Rh phenotype but give weak or negative reactions with Rh null erythrocytes, were used in quantitative binding assays and competitive binding assays to investigate the abundance and organization of polypeptides involved in the expression of antigens of the Rh blood group system. Antibodies of the R6A-type (R6A, BRIC-69, BRIC-207) and the 2D10-type (MB-2D10, LA18.18, LA23.40) recognize related structures and 100,000-200,000 molecules of each antibody bind maximally to erythrocytes of common Rh phenotype. Antibodies of the BRIC-125 type (BRICs 32, 122, 125, 126, 168, 211) recognize structures that are unrelated to those recognized by R6A-type and 2D10-type antibodies and between 10,000 and 50,000 antibody molecules bind maximally to erythrocytes of the common Rh phenotype. The binding of antibodies of the R6A-type and the 2D10-type, but not of antibodies of the BRIC-125-type could be partially inhibited by human anti-D antibodies (polyclonal and monoclonal) and a murine anti-e-like antibody. These results are consistent with evidence (Moore & Green 1987; Avent et al., 1988b) that the Rh blood group antigens are associated with a complex that comprises two groups of related polypeptides of M(r) 30,000 and M(r) 35,000-100,000, respectively, and suggest that there are 1-2 x 10(5) copies of this complex per erythrocyte. The polypeptide recognized by antibodies of the BRIC-125 type is likely to be associated with this complex. PMID:9259831

  13. Molecular characterization of dissolved organic matter in glacial ice: coupling natural abundance 1H NMR and fluorescence spectroscopy.

    PubMed

    Pautler, Brent G; Woods, Gwen C; Dubnick, Ashley; Simpson, André J; Sharp, Martin J; Fitzsimons, Sean J; Simpson, Myrna J

    2012-04-01

    Glaciers and ice sheets are the second largest freshwater reservoir in the global hydrologic cycle, and the onset of global climate warming has necessitated an assessment of their contributions to sea-level rise and the potential release of nutrients to nearby aquatic environments. In particular, the release of dissolved organic matter (DOM) from glacier melt could stimulate microbial activity in both glacial ecosystems and adjacent watersheds, but this would largely depend on the composition of the material released. Using fluorescence and (1)H NMR spectroscopy, we characterize DOM at its natural abundance in unaltered samples from a number of glaciers that differ in geographic location, thermal regime, and sample depth. Parallel factor analysis (PARAFAC) modeling of DOM fluorophores identifies components in the ice that are predominantly proteinaceous in character, while (1)H NMR spectroscopy reveals a mixture of small molecules that likely originate from native microbes. Spectrofluorescence also reveals a terrestrial contribution that was below the detection limits of NMR; however, (1)H nuclei from levoglucosan was identified in Arctic glacier ice samples. This study suggests that the bulk of the DOM from these glaciers is a mixture of biologically labile molecules derived from microbes. PMID:22385100

  14. Optical band gaps of organic semiconductor materials

    NASA Astrophysics Data System (ADS)

    Costa, José C. S.; Taveira, Ricardo J. S.; Lima, Carlos F. R. A. C.; Mendes, Adélio; Santos, Luís M. N. B. F.

    2016-08-01

    UV-Vis can be used as an easy and forthright technique to accurately estimate the band gap energy of organic π-conjugated materials, widely used as thin films/composites in organic and hybrid electronic devices such as OLEDs, OPVs and OFETs. The electronic and optical properties, including HOMO-LUMO energy gaps of π-conjugated systems were evaluated by UV-Vis spectroscopy in CHCl3 solution for a large number of relevant π-conjugated systems: tris-8-hydroxyquinolinatos (Alq3, Gaq3, Inq3, Al(qNO2)3, Al(qCl)3, Al(qBr)3, In(qNO2)3, In(qCl)3 and In(qBr)3); triphenylamine derivatives (DDP, p-TTP, TPB, TPD, TDAB, m-MTDAB, NPB, α-NPD); oligoacenes (naphthalene, anthracene, tetracene and rubrene); oligothiophenes (α-2T, β-2T, α-3T, β-3T, α-4T and α-5T). Additionally, some electronic properties were also explored by quantum chemical calculations. The experimental UV-Vis data are in accordance with the DFT predictions and indicate that the band gap energies of the OSCs dissolved in CHCl3 solution are consistent with the values presented for thin films.

  15. Metal oxide charge transport material doped with organic molecules

    DOEpatents

    Forrest, Stephen R.; Lassiter, Brian E.

    2016-08-30

    Doping metal oxide charge transport material with an organic molecule lowers electrical resistance while maintaining transparency and thus is optimal for use as charge transport materials in various organic optoelectronic devices such as organic photovoltaic devices and organic light emitting devices.

  16. Titan's inventory of organic surface materials

    NASA Astrophysics Data System (ADS)

    Lorenz, Ralph D.; Mitchell, Karl L.; Kirk, Randolph L.; Hayes, Alexander G.; Aharonson, Oded; Zebker, Howard A.; Paillou, Phillipe; Radebaugh, Jani; Lunine, Jonathan I.; Janssen, Michael A.; Wall, Stephen D.; Lopes, Rosaly M.; Stiles, Bryan; Ostro, Steve; Mitri, Giuseppe; Stofan, Ellen R.

    2008-01-01

    Cassini RADAR observations now permit an initial assessment of the inventory of two classes, presumed to be organic, of Titan surface materials: polar lake liquids and equatorial dune sands. Several hundred lakes or seas have been observed, of which dozens are each estimated to contain more hydrocarbon liquid than the entire known oil and gas reserves on Earth. Dark dunes cover some 20% of Titan's surface, and comprise a volume of material several hundred times larger than Earth's coal reserves. Overall, however, the identified surface inventories (>3 × 104 km3 of liquid, and >2 × 105 km3 of dune sands) are small compared with estimated photochemical production on Titan over the age of the solar system. The sand volume is too large to be accounted for simply by erosion in observed river channels or ejecta from observed impact craters. The lakes are adequate in extent to buffer atmospheric methane against photolysis in the short term, but do not contain enough methane to sustain the atmosphere over geologic time. Unless frequent resupply from the interior buffers this greenhouse gas at exactly the right rate, dramatic climate change on Titan is likely in its past, present and future.

  17. Assessment of Hybrid Organic-Inorganic Antimony Sulfides for Earth-Abundant Photovoltaic Applications.

    PubMed

    Yang, Ruo Xi; Butler, Keith T; Walsh, Aron

    2015-12-17

    Hybrid organic-inorganic solar absorbers are currently the subject of intense interest; however, the highest-performing materials contain Pb. Here we assess the potential of three Sb-based semiconductors: (i) Sb2S3, (ii) Cs2Sb8S13, and (iii) (CH3NH3)2Sb8S13. While the crystal structure of Sb2S3 is composed of 1D chains, 2D layers are formed in the ternary cesium and hybrid methylammonium antimony sulfide compounds. In each case, a stereochemically active Sb 5s(2) lone pair is found, resulting in a distorted coordination environment for the Sb cations. The bandgap of the binary sulfide is found to increase, while the ionization potential also changes, upon transition to the more complex compounds. Based on the predicted electronic structure, device configurations are suggested to be suitable for photovoltaic applications. PMID:26624204

  18. Spatial variability in the abundance, composition, and age of organic matter in surficial sediments of the East China Sea

    NASA Astrophysics Data System (ADS)

    Wu, Ying; Eglinton, Timothy; Yang, Liyang; Deng, Bing; Montluçon, Daniel; Zhang, Jing

    2013-12-01

    the sources and fate of organic matter (OM) sequestered in continental margin sediments is of importance because the mode and efficiency of OM burial impact the carbon cycle and the regulation of atmospheric CO2 over long time scales. We carried out molecular (lignin-derived phenols from CuO oxidation), elemental, isotopic (δ13C, Δ14C), and sedimentological (grain size and mineral surface area) analyses in order to examine spatial variability in the abundance, source, age of surface sediments of the East China Sea. Higher terrigenous organic matter values were found in the main accumulating areas of fluvial sediments, including the Changjiang (Yangtze) Estuary and Zhejiang-Fujian coastal zone. Isotopic and biomarker data suggest that the sedimentary OM in the inner shelf region was dominated by aged (Δ14C = -423 ± 42‰) but relatively lignin-rich OM (Λ = 0.94 ± 0.57 mg/100 mg OC) associated with fine-grained sediments, suggesting important contributions from soils. In contrast, samples from the outer shelf, while of similar age (Δ14 C = -450 ± 99‰), are lignin poor (Λ = 0.25 ± 0.14 mg/100 mg OC) and associated with coarse-grained material. Regional variation of lignin phenols and OM ages indicates that OM content is fundamentally controlled by hydrodynamic sorting (especially, sediment redistribution and winnowing) and in situ primary production. Selective sorption of acid to aldehyde in clay fraction also modified the ratios of lignin phenols. The burial of lignin in East China Sea is estimated to be relatively efficient, possibly as a consequence of terrigenous OM recalcitrance and/or relatively high sedimentation rates in the Changjiang Estuary and the adjacent Zhejing-Fujian mud belt.

  19. Removal of organic contaminants from lithographic materials

    NASA Astrophysics Data System (ADS)

    Lytle, Wayne M.

    One of the critical issues still facing the implementation of extreme ultraviolet lithography (EUVL) into mainstream manufacturing for integrated circuit (IC) production is cleanliness. EUV photons at 13.5 nm are easily absorbed by many species, including dust, thin-film layers, and other debris present in the path of the photons. Carrying out EUVL inside a vacuum helps reduce the amount of photon loss for illumination, however contamination in the sys- tem is unavoidable, especially due to carbon growth on the multilayer mirror collectors and to soft defects in the form of organic contamination on the mask. Traditional cleaning methods employ the use of wet chemicals to etch contamination off of a surface, however this is limited in the sub-micron range of contaminant particles due to lack of transport of sufficient liquid chemical to the surface in order to achieve satisfactory particle removal. According to the International Technology Roadmap for Semiconductors (ITRS), the photomask must be particle free at inspection below 30 nm. However, when analyzing the ability of traditional methods to meet the cleaning needs set forth by the ITRS, these methods fall short and often add more contamination to the surface targeted for cleaning. With that in mind, a new cleaning method is being developed to supplant these traditional methods. Preliminary research into a plasma-based method to clean organic contaminants from lithographic materials constructed an experimental device that demonstrated the removal of both polystyrene latex nanoparticles (representing hydrocarbon contamination) in the range of 30 nm to 500 nm, as well as the removal of 30 nm carbon film layers on silicon wafers. This research, called the Plasma-Assisted Cleaning by Metastable Atomic Neutralization (PACMAN) process is being developed with semiconductor manufacturing cleaning in mind. A model of the helium metastable density within the processing chamber has been developed in addition to

  20. Porphyrin Based Near Infrared-Absorbing Materials for Organic Photovoltaics

    NASA Astrophysics Data System (ADS)

    Zhong, Qiwen

    The conservation and transformation of energy is essential to the survival of mankind, and thus concerns every modern society. Solar energy, as an everlasting source of energy, holds one of the key solutions to some of the most urgent problems the world now faces, such as global warming and the oil crisis. Advances in technologies utilizing clean, abundant solar energy, could be the steering wheel of our societies. Solar cells, one of the major advances in converting solar energy into electricity, are now capturing people's interest all over the globe. While solar cells have been commercially available for many years, the manufacturing of solar cells is quite expensive, limiting their broad based implementation. The cost of solar cell based electricity is 15-50 cents per kilowatt hour (¢/kwh), depending on the type of solar cell, compared to 0.7 ¢/kwh for fossil fuel based electricity. Clearly, decreasing the cost of electricity from solar cells is critical for their wide spread deployment. This will require a decrease in the cost of light absorbing materials and material processing used in fabricating the cells. Organic photovoltaics (OPVs) utilize organic materials such as polymers and small molecules. These devices have the advantage of being flexible and lower cost than conventional solar cells built from inorganic semiconductors (e.g. silicon). The low cost of OPVs is tied to lower materials and fabrication costs of organic cells. However, the current power conversion efficiencies of OPVs are still below 15%, while convention crystalline Si cells have efficiencies of 20-25%. A key limitation in OPVs today is their inability to utilize the near infrared (NIR) portion of the solar spectrum. This part of the spectrum comprises nearly half of the energy in sunlight that could be used to make electricity. The first and foremost step in conversion solar energy conversion is the absorption of light, which nature has provided us optimal model of, which is

  1. Enzymatic activities and prokaryotic abundance in relation to organic matter along a West-East Mediterranean transect (TRANSMED cruise).

    PubMed

    Zaccone, R; Boldrin, A; Caruso, G; La Ferla, R; Maimone, G; Santinelli, C; Turchetto, M

    2012-07-01

    The distribution of extracellular enzymatic activities (EEA) [leucine aminopeptidase (LAP), ß-glucosidase (GLU), alkaline phosphatase (AP)], as well as that of prokaryotic abundance (PA) and biomass (PB), dissolved organic carbon (DOC), particulate organic carbon and particulate total nitrogen (POC, PTN), was determined in the epi-, meso-, and bathypelagic waters of the Mediterranean Sea along a West-East transect and at one Atlantic station located outside the Strait of Gibraltar. This study represents a synoptical evaluation of the microbial metabolism during early summer. Decreasing trends with depth were observed for most of the parameters (PA, PB, AP, DOC, POC, PTN). Significant differences between the western and eastern basins of the Mediterranean Sea were found, displaying higher rates of LAP and GLU and lower C/N ratios more in the eastern than in the western areas. Conversely, in the epipelagic layer, PA and PB were found to be higher in the western than in the eastern basins. PB was significantly related to DOC concentration (all data, n = 145, r = 0.53, P < 0.01), while significant correlations of EEA with POC and PTN were found in the epipelagic layer, indicating an active response of microbial metabolism to organic substrates. Specific enzyme activities normalized to cell abundance pointed out high values of LAP and GLU in the bathypelagic layer, especially in the eastern basin, while cell-specific AP was high in the epi- and bathypelagic zone of the eastern basin indicating a rapid regeneration of inorganic P for both prokaryotes and phytoplankton needs. Low activity and abundance characterized the Atlantic station, while opposite trends of these parameters were observed along the Mediterranean transect, showing the uncoupling between abundance and activity data. In the east Mediterranean Sea, decomposition processes increased probably in response to mesoscale structures which lead to organic matter downwelling. PMID:22349935

  2. Metal-organic framework materials with ultrahigh surface areas

    SciTech Connect

    Farha, Omar K.; Hupp, Joseph T.; Wilmer, Christopher E.; Eryazici, Ibrahim; Snurr, Randall Q.; Gomez-Gualdron, Diego A.; Borah, Bhaskarjyoti

    2015-12-22

    A metal organic framework (MOF) material including a Brunauer-Emmett-Teller (BET) surface area greater than 7,010 m.sup.2/g. Also a metal organic framework (MOF) material including hexa-carboxylated linkers including alkyne bond. Also a metal organic framework (MOF) material including three types of cuboctahedron cages fused to provide continuous channels. Also a method of making a metal organic framework (MOF) material including saponifying hexaester precursors having alkyne bonds to form a plurality of hexa-carboxylated linkers including alkyne bonds and performing a solvothermal reaction with the plurality of hexa-carboxylated linkers and one or more metal containing compounds to form the MOF material.

  3. Optoelectronic and Defect Properties in Earth Abundant Photovoltaic Materials: First-principle Calculations

    NASA Astrophysics Data System (ADS)

    Shi, Tingting

    In this dissertation, a series of earth-abundant photovoltaic materials including lead halide perovskites, copper based compounds, and silicon are investigated via density functional theory (DFT). Firstly, we study the unique optoelectronic properties of perovskite CH3NH3PbI3 and CH3NH3PbBr 3. First-principle calculations show that CH3NH3PbI 3 perovskite solar cells exhibit remarkable optoelectronic properties that account for the high open circuit voltage (Voc) and long electron-hole diffusion lengths. Our results reveal that for intrinsic doping, dominant point defects produce only shallow levels. Therefore lead halide perovskites are expected to exhibit intrinsic low non-radiative recombination rates. The conductivity of perovskites can be tuned from p-type to n-type by controlling the growth conditions. For extrinsic defects, the p-type perovskites can be achieved by doping group-IA, -IB, or -VIA elements, such as Na, K, Rb, Cu, and O at I-rich growth conditions. We further show that despite a large band gap of 2.2 eV, the dominant defects in CH3 NH3PbBr3 also create only shallow levels. The photovoltaic properties of CH3NH3PbBr3 - based perovskite absorbers can be tuned via defect engineering. Highly conductive p-type CH3NH3PbBr3 can be synthesized under Br-rich growth conditions. Such CH3NH3PbBr 3 may be potential low-cost hole transporting materials for lead halide perovskite solar cells. All these unique defect properties of perovskites are largely due to the strong Pb lone-pair s orbital and I p (Br p) orbital antibonding coupling and the high ionicity of CH3NH3PbX3 (X=I, Br). Secondly, we study the optoelectronic properties of Cu-V-VI earth abundant compounds. These low cost thin films may have the good electronic and optical properties. We have studied the structural, electronic and optical properties of Cu3-V-VI4 compounds. After testing four different crystal structures, enargite, wurtzite-PMCA, famatinite and zinc-blend-PMCA, we find that Cu3PS4 and

  4. Factors controlling the abundance of organic sulfur in flash pyrolyzates of Upper Cretaceous kerogens from Sergipe Basin, Brazil

    USGS Publications Warehouse

    Carmo, A.M.; Stankiewicz, B.A.; Mastalerz, Maria; Pratt, L.M.

    1997-01-01

    The molecular and elemental composition of immature kerogens isolated from Upper Cretaceous marine carbonates from Sergipe Basin, Brazil were investigated using combined pyrolysis-gas chromatography/mass spectrometry and organic petrographic techniques. The kerogens are predominantly composed of reddish-fluorescing amorphous organic matter (AOM) and variable amounts of yellow-fluorescing alginite and liptodetrinite. The abundance of organic sulfur in the kerogens inferred from the ratio 2-ethyl-5-methylthiophene/(1,2-dimethylbenzene + dec-1-ene) in the pyrolyzates is variable and may be related to changes in the type of primary organic input and/or to variations in rates of bacterial sulfate reduction. A concomitant increase in S/C and O/C ratios determined in situ using the electron microprobe is observed in AOM and alginites and may be related to a progressive oxidation of the organic matter during sulfurization. The S/C ratio of the AOM is systematically higher than the S C ratio of the alginites. Combined with a thiophene distribution characteristic of pyrolyzates of Type II organic matter, the higher S/C of AOM in Sergipe kerogens suggests that sulfurization and incorporation of low-molecular weight lipids derived from normal marine organic matter into the kerogen structure predominated over direct sulfurization of highly aliphatic algal biomacromolecules.The molecular and elemental composition of immature kerogens isolated from Upper Cretaceous marine carbonates from Sergipe Basin, Brazil were investigated using combined pyrolysis-gas chromatography/mass spectrometry and organic petrographic techniques. The kerogens are predominantly composed of reddish-fluorescing amorphous organic matter (AOM) and variable amounts of yellow-fluorescing alginite and liptodetrinite. The abundance of organic sulfur in the kerogens inferred from the ratio 2-ethyl-5-methylthiophene/(1,2-dimethylbenzene+dec-1-ene) in the pyrolyzates is variable and may be related to changes in

  5. Apparatus and method for constant flow oxidizing of organic materials

    DOEpatents

    Surma, Jeffrey E.; Nelson, Norvell; Steward, G. Anthony; Bryan, Garry H.

    1999-01-01

    The invention is a method and apparatus using high cerium concentration in the anolyte of an electrochemical cell to oxidize organic materials. The method and apparatus further use an ultrasonic mixer to enhance the oxidation rate of the organic material in the electrochemical cell. A reaction vessel provides an advantage of independent reaction temperature control and electrochemical cell temperature control. A separate or independent reaction vessel may be used without an ultrasonic mixer to oxidize gaseous phase organic materials.

  6. Formation kinetics and abundance of organic nitrates in α-pinene ozonolysis

    NASA Astrophysics Data System (ADS)

    Berkemeier, Thomas; Ammann, Markus; Pöschl, Ulrich; Shiraiwa, Manabu

    2016-04-01

    Formation of organic nitrates affects the total atmospheric budget of oxidized nitrogen (NOy) and alters the total aerosol mass yield from secondary sources. We investigated the formation of organic nitrate species during ozonolysis of α-pinene and subsequent formation of secondary organic aerosols (SOA) using the short-lived radioactive tracer 13N inside an aerosol flow reactor (Ammann et al., 2001). The results represent direct measurements of the organic nitrate content of α-pinene secondary aerosol and give insight into the kinetics of organic nitrate formation. Organic nitrates constituted up to 40 % of aerosol mass with a pronounced influence during the initial period of particle growth. Kinetic modelling, as well as additional experiments using OH scavengers and UV irradiation, suggests that organic peroxy radicals (RO2) from the reaction of α-pinene with secondarily produced OH are important intermediates in the organic nitrate formation process. Direct oxidation of α-pinene by NO3 was found to be a less efficient pathway for formation of particle phase nitrate. The organic nitrate content decreased very slightly with an increase of relative humidity on the experimental time scale. The experiments show a tight correlation between organic nitrate content and SOA number concentrations, implying that organic nitrates play an important role in nucleation and growth of nanoparticles. Since present in large amounts in organic aerosol, organic nitrates deposited in the lung might have implications for human health as they release nitric acid upon hydrolysis, especially in regions influenced by urban pollution and large sources of monoterpene SOA precursors. References Ammann et al. (2001) Radiochimica Acta 89, 831.

  7. Fabricating porous materials using interpenetrating inorganic-organic composite gels

    DOEpatents

    Seo, Dong-Kyun; Volosin, Alex

    2016-06-14

    Porous materials are fabricated using interpenetrating inorganic-organic composite gels. A mixture or precursor solution including an inorganic gel precursor, an organic polymer gel precursor, and a solvent is treated to form an inorganic wet gel including the organic polymer gel precursor and the solvent. The inorganic wet gel is then treated to form a composite wet gel including an organic polymer network in the body of the inorganic wet gel, producing an interpenetrating inorganic-organic composite gel. The composite wet gel is dried to form a composite material including the organic polymer network and an inorganic network component. The composite material can be treated further to form a porous composite material, a porous polymer or polymer composite, a porous metal oxide, and other porous materials.

  8. Elastomeric organic material for switching application

    SciTech Connect

    Shiju, K. E-mail: pravymon@gmail.com Praveen, T. E-mail: pravymon@gmail.com Preedep, P. E-mail: pravymon@gmail.com

    2014-10-15

    Organic Electronic devices like OLED, Organic Solar Cells etc are promising as, cost effective alternatives to their inorganic counterparts due to various reasons. However the organic semiconductors currently available are not attractive with respect to their high cost and intricate synthesis protocols. Here we demonstrate that Natural Rubber has the potential to become a cost effective solution to this. Here an attempt has been made to fabricate iodine doped poly isoprene based switching device. In this work Poly methyl methacrylate is used as dielectric layer and Aluminium are employed as electrodes.

  9. Accounting for non-independent detection when estimating abundance of organisms with a Bayesian approach

    USGS Publications Warehouse

    Martin, Julien; Royle, J. Andrew; MacKenzie, Darryl I.; Edwards, Holly H.; Kery, Marc; Gardner, Beth

    2011-01-01

    Summary 1. Binomial mixture models use repeated count data to estimate abundance. They are becoming increasingly popular because they provide a simple and cost-effective way to account for imperfect detection. However, these models assume that individuals are detected independently of each other. This assumption may often be violated in the field. For instance, manatees (Trichechus manatus latirostris) may surface in turbid water (i.e. become available for detection during aerial surveys) in a correlated manner (i.e. in groups). However, correlated behaviour, affecting the non-independence of individual detections, may also be relevant in other systems (e.g. correlated patterns of singing in birds and amphibians). 2. We extend binomial mixture models to account for correlated behaviour and therefore to account for non-independent detection of individuals. We simulated correlated behaviour using beta-binomial random variables. Our approach can be used to simultaneously estimate abundance, detection probability and a correlation parameter. 3. Fitting binomial mixture models to data that followed a beta-binomial distribution resulted in an overestimation of abundance even for moderate levels of correlation. In contrast, the beta-binomial mixture model performed considerably better in our simulation scenarios. We also present a goodness-of-fit procedure to evaluate the fit of beta-binomial mixture models. 4. We illustrate our approach by fitting both binomial and beta-binomial mixture models to aerial survey data of manatees in Florida. We found that the binomial mixture model did not fit the data, whereas there was no evidence of lack of fit for the beta-binomial mixture model. This example helps illustrate the importance of using simulations and assessing goodness-of-fit when analysing ecological data with N-mixture models. Indeed, both the simulations and the goodness-of-fit procedure highlighted the limitations of the standard binomial mixture model for aerial

  10. Occurrence and abundance of carbohydrates and amino compounds in sequentially extracted labile soil organic matter fractions.

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This study aimed to investigate the content of carbohydrates and amino compounds in three labile fraction of soil organic matter (SOM). Soil samples were collected from two agricultural fields in southern Italy and the light fraction (LF), the 500–53-µm particulate organic matter (POM) and the mobil...

  11. Weed seed persistence and microbial abundance in long-term organic and conventional cropping systems

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Weed seed persistence in soil can be influenced by many factors, including crop management. This research was conducted to determine whether organic management systems with higher organic amendments and soil microbial biomass could reduce weed seed persistence compared to conventional management sy...

  12. Distribution and abundance of benthic organisms in the Sacramento River, California

    USGS Publications Warehouse

    Ferreira, Rodger F.; Green, D. Brady

    1977-01-01

    General comparisons were made between benthic organism samples collected in 1960-61 and 1972-73 from five sites in the Sacramento River between Red Bluff and Knights Landing, Calif. The composition of benthic organisms from both collection periods was similar. The 1972-73 data showed variable patterns in monthly changes at each site and downstream changes each month with number of organisms per square meter, number of taxa per square meter, and diversity index. Generally, the mean number of taxa per square meter and diversity index for all sampling periods were higher in the upper reach than the lower reach of the Sacramento River. (Woodard-USGS)

  13. X-ray characterization of solid small molecule organic materials

    SciTech Connect

    Billinge, Simon; Shankland, Kenneth; Shankland, Norman; Florence, Alastair

    2014-06-10

    The present invention provides, inter alia, methods of characterizing a small molecule organic material, e.g., a drug or a drug product. This method includes subjecting the solid small molecule organic material to x-ray total scattering analysis at a short wavelength, collecting data generated thereby, and mathematically transforming the data to provide a refined set of data.

  14. THE ORGANIZATION OF NONBOOK MATERIALS IN SCHOOL LIBRARIES.

    ERIC Educational Resources Information Center

    HICKS, WARREN B.; TILLIN, ALMA M.

    A GENERAL GUIDE FOR CATALOGING AND PROCESSING OF NON-BOOK MATERIALS, THIS MANUAL WAS WRITTEN IN RESPONSE TO REQUESTS FOR ASSISTANCE IN ORGANIZING AUDIO-VISUAL MATERIALS FOR USE BY PUPILS AND TEACHERS IN CALIFORNIA SCHOOL LIBRARIES. AS SUCH, THE DECISIONS ON CATALOGING PROCEDURE ARE BASED UPON THE PRINCIPLE THAT THE ORGANIZATION OF ALL…

  15. Pesticide sorption on geologic material of varying organic carbon content.

    PubMed

    Bouchard, D C; Wood, A L

    1988-09-01

    Sorption of three pesticides on geologic material ranging in organic carbon content from 0.33 to 6.9 g kg-1 was measured in soil columns using a miscible displacement technique. An octanol-water partitioning model was shown to be inappropriate for predicting sorption of the less hydrophobic pesticides on the low organic carbon materials. PMID:3255290

  16. Continuous extraction of organic materials from water

    USGS Publications Warehouse

    Goldberg, M.C.; DeLong, L.; Kahn, L.

    1971-01-01

    A continuous liquid solvent extractor, designed to utilize organic solvents that are heavier than water, is described. The extractor is capable of handling input rates up to 2 liters per hour and has a 500-ml. extractant capacity. Extraction efficiency is dependent upon the p-value, the two solvent ratios, rate of flow of the aqueous phase, and rate of reflux of the organic phase. Extractors can be serially coupled to increase extraction efficiency and, when coupled with a lighter-than-water extractor, the system will allow the use of any immiscible solvent.

  17. Process for hot briquetting of organic solid materials

    SciTech Connect

    Janusch, A.

    1982-11-23

    For the purpose of briquetting organic solid materials, such as brown coal or bituminous coal, the materials are heated by hot water and/or steam and under super-atmospheric pressure to temperatures exceeding 160/sup 0/ C. After discharging the organic solid materials, which have become dried to a great extent, the generated steam is separated by sucking off the steam without substantially cooling effect, bitumen-forming substances present within the organic solid materials thereby rapidly becoming homogeneously distributed. These homogeneously distributed binding agents give the compressed briquettes obtained a high strength and good mechanical properties when using substantially reduced compacting pressures as compared with known briquetting processes.

  18. Laboratory reflectance spectra of clay minerals mixed with Mars analog materials: Toward enabling quantitative clay abundances from Mars spectra

    NASA Astrophysics Data System (ADS)

    Roush, Ted L.; Bishop, Janice L.; Brown, Adrian J.; Blake, David F.; Bristow, Thomas F.

    2015-09-01

    Quantitative estimates of clay minerals on the martian surface, via remote sensing observations, provide constraints on activity, timing, duration, and extent of aqueous processes and the geochemical environment in martian history. We describe an analytical study to begin enabling quantitative estimates of phyllosilicates when mixed with martian analog materials. We characterize the chemistry, mineralogy, particle size distribution, and reflectance spectra of the end-member materials: saponite, montmorillonite, pyroxene, and palagonitic soil. Reflectance spectra were obtained for physical mixtures of saponite and montmorillonite with pyroxene, and saponite with palagonitic soil. We analyzed the diagnostic phyllosilicate spectral signatures in the 2.2-2.4 μm wavelength region in detail for the mixtures. This involved fitting the observed ∼2.3 or ∼2.2 μm band depth, associated with the presence of saponite and montmorillonite, respectively, as a function of the abundance of these materials in the mixtures. Based upon the band depth of the spectral features we find that 3-5 wt.% of the clay minerals in the mixture with pyroxene can be recognized and at 25 wt.% their presence is indisputable in the mixtures. When the saponite is mixed with the lower albedo palagonitic soil, its presence is clearly distinguishable via the 1.4 and 2.3 μm features at 25 wt.% abundance. These relationships, between abundance and band depth, provide an ability to quantitatively address the amount of these materials in mixtures. The trends described here provide guidance for estimating the presence of phyllosilicates in matrices on the martian surface.

  19. EDITORIAL Light-induced material organization Light-induced material organization

    NASA Astrophysics Data System (ADS)

    Vainos, Nikos; Rode, Andrei V.

    2010-12-01

    Light-induced material organization extends over a broad area of research, from photon momentum transfer to atoms, molecules and particles, serving the basis for optical trapping, and expands into the laser-induced changes of material properties through photopolymerization, photodarkening, and materials ablation. Relevant phenomena are observed over many orders of magnitude of light intensity, from a few kW cm-2 for the optical trapping of living cells to 1014 W cm-2 encountered in femtosecond laser micromachining and micro-explosion. Relevant interactions reveal a rich palette of novel phenomena in the solid state, from subtle excitations and material organization to phase transformations, non-equilibrium and transient states. The laser-induced material modifications relate to changes in the crystal structure and the molecular bonding, phase transitions in liquid state, ablation and plasma production associated with extreme pressure and temperature conditions towards entirely new states of matter. The underlying physical mechanisms form the foundations for micro-engineering photonic and other functional devices and lead the way to relevant applications. At the same time, they hold the potential for creating non-equilibrium material states and a range of fundamentally new products not available by other means. The fundamental understanding of both materials nature and functional behaviour will ultimately yield novel devices and improved performance in several fields. The far reaching goals of these studies relate to the development of new methods and technologies for micro- and nano-fabrication, not only offering a significant reduction of cost, but also expanding the fabrication capabilities into unexplored areas of biophotonics and nanotechnology. This special issue of Journal of Optics presents some very recent and exciting advances in the field of materials manipulation by laser beams, aiming to underline its current trends. In optical trapping research we

  20. Flexible Organic Electronics in Biology: Materials and Devices.

    PubMed

    Liao, Caizhi; Zhang, Meng; Yao, Mei Yu; Hua, Tao; Li, Li; Yan, Feng

    2015-12-01

    At the convergence of organic electronics and biology, organic bioelectronics attracts great scientific interest. The potential applications of organic semiconductors to reversibly transmit biological signals or stimulate biological tissues inspires many research groups to explore the use of organic electronics in biological systems. Considering the surfaces of movable living tissues being arbitrarily curved at physiological environments, the flexibility of organic bioelectronic devices is of paramount importance in enabling stable and reliable performances by improving the contact and interaction of the devices with biological systems. Significant advances in flexible organic bio-electronics have been achieved in the areas of flexible organic thin film transistors (OTFTs), polymer electrodes, smart textiles, organic electrochemical ion pumps (OEIPs), ion bipolar junction transistors (IBJTs) and chemiresistors. This review will firstly discuss the materials used in flexible organic bioelectronics, which is followed by an overview on various types of flexible organic bioelectronic devices. The versatility of flexible organic bioelectronics promises a bright future for this emerging area. PMID:25393596

  1. Metal-Organic Frameworks as Platforms for Functional Materials.

    PubMed

    Cui, Yuanjing; Li, Bin; He, Huajun; Zhou, Wei; Chen, Banglin; Qian, Guodong

    2016-03-15

    Discoveries of novel functional materials have played very important roles to the development of science and technologies and thus to benefit our daily life. Among the diverse materials, metal-organic framework (MOF) materials are rapidly emerging as a unique type of porous and organic/inorganic hybrid materials which can be simply self-assembled from their corresponding inorganic metal ions/clusters with organic linkers, and can be straightforwardly characterized by various analytical methods. In terms of porosity, they are superior to other well-known porous materials such as zeolites and carbon materials; exhibiting extremely high porosity with surface area up to 7000 m(2)/g, tunable pore sizes, and metrics through the interplay of both organic and inorganic components with the pore sizes ranging from 3 to 100 Å, and lowest framework density down to 0.13 g/cm(3). Such unique features have enabled metal-organic frameworks to exhibit great potentials for a broad range of applications in gas storage, gas separations, enantioselective separations, heterogeneous catalysis, chemical sensing and drug delivery. On the other hand, metal-organic frameworks can be also considered as organic/inorganic self-assembled hybrid materials, we can take advantages of the physical and chemical properties of both organic and inorganic components to develop their functional optical, photonic, and magnetic materials. Furthermore, the pores within MOFs can also be utilized to encapsulate a large number of different species of diverse functions, so a variety of functional MOF/composite materials can be readily synthesized. In this Account, we describe our recent research progress on pore and function engineering to develop functional MOF materials. We have been able to tune and optimize pore spaces, immobilize specific functional groups, and introduce chiral pore environments to target MOF materials for methane storage, light hydrocarbon separations, enantioselective recognitions

  2. Pyrolysis Mass Spectrometry of Complex Organic Materials.

    ERIC Educational Resources Information Center

    Meuzelaar, Henk L. C.; And Others

    1984-01-01

    Illustrates the state of the art in pyrolysis mass spectrometry techniques through applications in: (1) structural determination and quality control of synthetic polymers; (2) quantitative analysis of polymer mixtures; (3) classification and structural characterization of fossil organic matter; and (4) nonsupervised numerical extraction of…

  3. Simple Test For Organic Material In Gas

    NASA Technical Reports Server (NTRS)

    Barzana, Eduardo; Klibanov, Alexander; Karel, Marcus

    1989-01-01

    Dried enzymes and color indicators test sensitively and selectively. Dehydrated enzymes used in convenient method for analyzing gases for specific organic substances, outside laboratory. Method used to detect alcohol in breath or formaldehyde in gas streams. Used for simple semiquantitative detection or for precise quantitative measurement.

  4. Organic polymer materials in the space environment

    NASA Astrophysics Data System (ADS)

    Chen, Jun; Ding, Nengwen; Li, Zhifeng; Wang, Wei

    2016-05-01

    The space environment is a complex environment full of microgravity, high vacuum, high and low temperature, strong radiation and plasma. Polymers used in the space environment will inevitably experience aging and degradation which result in changes of the material mechanics, physics and chemical properties, until they lose usefulness. To make a material that can be used for a long time and whose performance is not changed in the space environment, its ability to resist environmental factors must be excellent. Therefore, this paper provides an introduction to the harmful conditions in the space environment and their effects on the polymers, also it reviews the aging mechanisms of the adhesives used in the space environment and the effect of thermal cycling, stress, electromagnetic radiation and ionizing particles on the properties of polymers and optical devices, to provide the reference basis for selection, modification and reliability analysis of materials used in the space environment.

  5. Photoconversion of gasified organic materials into biologically-degradable plastics

    DOEpatents

    Weaver, Paul F.; Maness, Pin-Ching

    1993-01-01

    A process is described for converting organic materials (such as biomass wastes) into a bioplastic suitable for use as a biodegradable plastic. In a preferred embodiment the process involves thermally gasifying the organic material into primarily carbon monoxide and hydrogen, followed by photosynthetic bacterial assimilation of the gases into cell material. The process is ideally suited for waste recycling and for production of useful biodegradable plastic polymer.

  6. Photoconversion of gasified organic materials into biologically-degradable plastics

    DOEpatents

    Weaver, P.F.; Pinching Maness.

    1993-10-05

    A process is described for converting organic materials (such as biomass wastes) into a bioplastic suitable for use as a biodegradable plastic. In a preferred embodiment the process involves thermally gasifying the organic material into primarily carbon monoxide and hydrogen, followed by photosynthetic bacterial assimilation of the gases into cell material. The process is ideally suited for waste recycling and for production of useful biodegradable plastic polymer. 3 figures.

  7. 78 FR 19637 - National Organic Program: Notice of Draft Guidance on Classification of Materials and Materials...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-04-02

    ...) Bulletin on Agency Good Guidance Practices (GGPs) (January 25, 2007, 72 FR 3432-3440). The purpose of GGPs... on Classification of Materials and Materials for Organic Crop Production AGENCY: Agricultural... materials used for organic crop production, livestock production, and handling. The second set of...

  8. Nonbook Materials: The Organization of Integrated Collections.

    ERIC Educational Resources Information Center

    Weihs, Jean Riddle; And Others

    This book has been written for all types of libraries and media centres which wish to have an omnimedia catalog, i.e., one in which the entries for all materials, both book and nonbook, are interfiled. In order to integrate all entries successfully the same cataloging principles should apply to all media. A practical solution is to enter and…

  9. Metal-Organic and Organic TADF-Materials: Status, Challenges and Characterization.

    PubMed

    Bergmann, Larissa; Zink, Daniel M; Bräse, Stefan; Baumann, Thomas; Volz, Daniel

    2016-06-01

    This section covers both metal-organic and organic materials that feature thermally activated delayed fluorescence (TADF). Such materials are especially useful for organic light-emitting diodes (OLEDs), a technology that was introduced in commercial displays only recently. We compare both material classes to show commonalities and differences, highlighting current issues and challenges. Advanced spectroscopic techniques as valuable tools to develop solutions to those issues are introduced. Finally, we provide an outlook over the field and highlight future trends. PMID:27573262

  10. Human Heart Mitochondrial DNA Is Organized in Complex Catenated Networks Containing Abundant Four-way Junctions and Replication Forks*

    PubMed Central

    Pohjoismäki, Jaakko L. O.; Goffart, Steffi; Tyynismaa, Henna; Willcox, Smaranda; Ide, Tomomi; Kang, Dongchon; Suomalainen, Anu; Karhunen, Pekka J.; Griffith, Jack D.; Holt, Ian J.; Jacobs, Howard T.

    2009-01-01

    Analysis of human heart mitochondrial DNA (mtDNA) by electron microscopy and agarose gel electrophoresis revealed a complete absence of the θ-type replication intermediates seen abundantly in mtDNA from all other tissues. Instead only Y- and X-junctional forms were detected after restriction digestion. Uncut heart mtDNA was organized in tangled complexes of up to 20 or more genome equivalents, which could be resolved to genomic monomers, dimers, and linear fragments by treatment with the decatenating enzyme topoisomerase IV plus the cruciform-cutting T7 endonuclease I. Human and mouse brain also contained a population of such mtDNA forms, which were absent, however, from mouse, rabbit, or pig heart. Overexpression in transgenic mice of two proteins involved in mtDNA replication, namely human mitochondrial transcription factor A or the mouse Twinkle DNA helicase, generated abundant four-way junctions in mtDNA of heart, brain, and skeletal muscle. The organization of mtDNA of human heart as well as of mouse and human brain in complex junctional networks replicating via a presumed non-θ mechanism is unprecedented in mammals. PMID:19525233

  11. Metal free earth abundant elemental red phosphorus: a new class of visible light photocatalyst and photoelectrode materials.

    PubMed

    Ansari, Sajid Ali; Ansari, Mohammad Shahnawaze; Cho, Moo Hwan

    2016-02-01

    Developing a high-performance photocatalyst and a photoelectrode with enhanced visible light harvesting properties is essential for practical visible light photocatalytic applications. Noble metal-free, highly visible light-active, elemental red phosphorus (RP) was prepared by a facile mechanical ball milling method, which is a reproducible, low cost and controllable synthesis process. The synthesis used inexpensive and abundant raw materials because most RP hybrids are based on expensive noble-metals. The novel milled RP showed significantly enhanced photocatalytic and photoelectrochemical performances with a lower charge transfer resistance compared to commercial RP under wide visible photoirradiation, making it a feasible alternative for photocatalytic applications. PMID:26765211

  12. Zirconium and hafnium abundances in some lunar materials and implications of their ratios

    NASA Technical Reports Server (NTRS)

    Chyi, L. L.; Ehmann, W. D.

    1973-01-01

    A new rapid and precise analytical procedure for Zr and Hf has been applied to the study of lunar materials. The results indicate that the Zr/Hf ratios in lunar materials vary in a narrow range from 36.6 to 51.3 while their respective contents vary by a factor of 40. There is a strong Zr, Hf, and major element correlation. This correlation and the Zr and Hf systematics suggest that lunar materials fall into two groups. One group characterized by high Zr and Hf contents and higher Zr/Hf ratios corresponds to materials with a high KREEP content; the other characterized by low Zr and Hf contents and lower Zr/Hf ratios corresponds to materials with high Ti, Fe, Mn, and Mg contents. We believe that the modest Zr and Hf fractionation we observe is related to the extent of stabilization of the metals in the early titanium minerals and a charge disparity under extremely reduced conditions in which Zr exists as 3+, while Hf remains as 4+.

  13. Efficient electrolyzer for CO2 splitting in neutral water using earth-abundant materials.

    PubMed

    Tatin, Arnaud; Comminges, Clément; Kokoh, Boniface; Costentin, Cyrille; Robert, Marc; Savéant, Jean-Michel

    2016-05-17

    Low-cost, efficient CO2-to-CO+O2 electrochemical splitting is a key step for liquid-fuel production for renewable energy storage and use of CO2 as a feedstock for chemicals. Heterogeneous catalysts for cathodic CO2-to-CO associated with an O2-evolving anodic reaction in high-energy-efficiency cells are not yet available. An iron porphyrin immobilized into a conductive Nafion/carbon powder layer is a stable cathode producing CO in pH neutral water with 90% faradaic efficiency. It is coupled with a water oxidation phosphate cobalt oxide anode in a home-made electrolyzer by means of a Nafion membrane. Current densities of approximately 1 mA/cm(2) over 30-h electrolysis are achieved at a 2.5-V cell voltage, splitting CO2 and H2O into CO and O2 with a 50% energy efficiency. Remarkably, CO2 reduction outweighs the concurrent water reduction. The setup does not prevent high-efficiency proton transport through the Nafion membrane separator: The ohmic drop loss is only 0.1 V and the pH remains stable. These results demonstrate the possibility to set up an efficient, low-voltage, electrochemical cell that converts CO2 into CO and O2 by associating a cathodic-supported molecular catalyst based on an abundant transition metal with a cheap, easy-to-prepare anodic catalyst oxidizing water into O2. PMID:27140621

  14. Abundance and diversity of total and nitrifying prokaryotes as influenced by biochemical quality of organic inputs combined with mineral nitrogen

    NASA Astrophysics Data System (ADS)

    Muema, Esther; Vanlauwe, Bernard; Röhl, Carolin; Cadisch, Georg; Rasche, Frank

    2014-05-01

    Ammonia-oxidizing bacteria and archaea (AOB, AOA) co-exist in soil, but they respond differently to distinct fertilization strategies in agricultural soils. Accordingly, effects of organic inputs and combination with mineral nitrogen (N) on AOB and AOA remain poorly understood. The aim of this study was to compare soil amendment with contrasting quality of organic inputs (i.e., high quality Tithonia diversifolia (TD; C/N ratio: 13, Lignin: 8.9 %; Polyphenols: 1.7 %), intermediate quality Calliandra calothyrsus (CC; 13; 13; 9.4) and low quality Zea mays (ZM; 59; 5.4; 1.2)), and combination with mineral N on the abundance (i.e., DNA-based gene quantification) and community structure (i.e., T-RFLP analysis) of total bacterial and archaea (16S rRNA gene), as well as AOB and AOA (targeting the amoA gene) communities in a Humic Nitisol. Soils (0-15 cm depth) were sampled prior to the onset of the rainy season in March 2012 in a 10 years old field experiment established in the central highlands of Kenya in 2002. Since the start of the experiment, organic inputs were applied annually at a rate of 4 Mg C ha-1 and mineral N twice a year as calcium ammonium nitrate (5Ca(NO3)2NH4NO3) at a rate of 120 kg N ha-1 growing season-1. Quality of organic inputs posed only a significant effect on the AOB community structure between TD versus ZM and CC versus ZM. Moreover, TD significantly increased the size of AOB over ZM input, while higher abundances for total bacteria, total archaea and AOA were measured in ZM and TD over CC. This was explained by high and available N in TD, but low lignin and polyphenol contents in TD and ZM as opposed to CC. AOB responded sensitively (i.e., complete community structure separation) to mineral N, specifically when combined with low quality ZM. Hence, AOB community was specifically responsive to quality of organic inputs and combination of low organic input with mineral N over AOA and total prokaryotic communities in the studied soil. The results

  15. Abundance and Characterization of Dissolved Organic Carbon in Suburban Streams of Baltimore, Maryland, USA

    NASA Astrophysics Data System (ADS)

    Mora, G.; Fazekas, M.

    2014-12-01

    The contribution of streams and rivers to the carbon cycle is significant, transporting to the oceans ~1.4 Pg C/yr, with dissolved carbon corresponding to as much as 0.7 Pg C/yr. Changes in land use have the potential effect of modifying this flux, particularly in urban areas where impervious areas are common. To investigate the effect of urbanization on riverine carbon transport, we studied four first-order streams in Towson, a suburb of Baltimore, Maryland, USA. The watersheds from the studied streams exhibit different levels of urbanization as measured by the percentage of impervious areas. Samples from these four streams were taken weekly, and several chemical constituents were measured either in the field or in the laboratory. These constituents included nitrate, dissolved organic nitrogen, pH, dissolved organic carbon (DOC), total carbon, dissolved inorganic carbon (DIC), phosphate, the carbon isotopic compositions of DOC and DIC, and fluorescence intensity of the DOC. Results show that DOC concentrations were consistently below 5 mg C/L regardless of the level of imperviousness of the watershed. Similarly, carbon isotope ratios were consistent across the studied streams, with values centered around -26.4 per mil, thus suggesting a significant influx of soil-derived organic carbon originated from C3 plants that are common in the watersheds. Confirming this interpretation, fluorescence spectroscopy data suggest a humic-like origin for the DOC of the streams, thus pointing to the heterotrophic nature of the streams. The combined results suggest that the studied streams exhibit similar DOC concentrations, carbon isotopic values, and fluorescence spectra, despite their level of impervious surfaces in their watersheds.

  16. Abundance of organic compounds photochemically produced in the atmospheres of the Outer Planets

    NASA Technical Reports Server (NTRS)

    Raulin, F.; Bossard, A.; Toupance, G.; Ponnamperuma, C.

    1979-01-01

    Organic photochemical syntheses in the Jovian atmosphere was simulated by irradiating, at 147 nm, gaseous mixtures of methane and ammonia with varying amounts of hydrogen. Some results relevant to the photochemistry of the Jupiter atmosphere at several tens of kilometers above the clouds were obtained: (1) a favorable effect of the pressure of high amounts of H2 on the yield of hydrocarbon synthesis when NH3 is mixed with CH4; (2) a very low yield of synthesis of unsaturated hydrocarbons in such conditions; and (3) the possibility of formation of detectable amounts of HCN and CH3CN.

  17. Development of organic nonlinear optical materials

    NASA Astrophysics Data System (ADS)

    Sounik, J.; Norwood, R.; McCulloch, I.; Song, K.; Demartino, R.

    1992-10-01

    The design of organic polymers as active mediums for nonlinear optics has attracted much attention because their nature of versatility in synthetic chemistry and in fabrication. A series of new side chain polymers were synthesized and characterized for the second and third order NLO applications. Linear copolymers containing maleic anhydride as an active functional group on the main chain were prepared in this work. The maleic anhydride group reacts, by ring opening esterification with an appropriate alcohol containing an NLO functionality. These copolymers were also found to be suitable for branching or crosslinking reactions with alpha, omega-diols. A series of substituted silicon and aluminum phthalocyanines has been synthesized to study their third order nonlinear responses. A nitro/amino substituted aluminum phthalocyanine has been made along with mixtures of benzo-substituted silicon phthalocyanines. A synthetic route has been investigated to directly give donor acceptor phthalocyanines. To increase mechanical property of phthalocyanine compounds, copolymers with MMA have been synthesized and characterized. All of the copolymers show excellent film forming characteristics.

  18. TOTAL ORGANIC CARBON DETERMINATIONS IN NATURAL AND CONTAMINATED AQUIFER MATERIALS

    EPA Science Inventory

    Quantifying the total organic carbon (TOC) content of soils and aquifer materials is essential for understanding subsurface chemistry during environmental site characterization. ontaminant fate and transport, microbial ecology, and effective treatment methodology are all influenc...

  19. Effect of flagellates on free-living bacterial abundance in an organically contaminated aquifer

    USGS Publications Warehouse

    Kinner, N.E.; Harvey, R.W.; Kazmierkiewicz-Tabaka, M.

    1997-01-01

    Little is known about the role of protists in the saturated subsurface. Porous media microcosms containing bacteria and protists, were used to determine whether flagellates from an organically contaminated aquifer could substantively affect the number of free- living bacteria (FLB). When flagellates were present, the 3-40% maximum breakthrough of fluorescent y labelled FLB injected into the microcosms was much lower than the 60-130% observed for killed controls Grazing and clearance rates (3-27 FLB flag-1 h-1 and 12-23 nI flag-1 h-1, respectively) calculated from the data were in the range reported for flagellates in other aqueous environments. The data provide evidence that flagellate bacterivory is an important control on groundwater FLB populations.

  20. Constraints on hydrocarbon and organic acid abundances in hydrothermal fluids at the Von Damm vent field, Mid-Cayman Rise (Invited)

    NASA Astrophysics Data System (ADS)

    McDermott, J. M.; Seewald, J.; German, C. R.; Sylva, S. P.

    2013-12-01

    The generation of organic compounds in vent fluids has been of interest since the discovery of seafloor hydrothermal systems, due to implications for the sustenance of present-day microbial populations and their potential role in the origin of life on early Earth. Possible sources of organic compounds in hydrothermal systems include microbial production, thermogenic degradation of organic material, and abiotic synthesis. Abiotic organic synthesis reactions may occur during active circulation of seawater-derived fluids through the oceanic crust or within olivine-hosted fluid inclusions containing carbon-rich magmatic volatiles. H2-rich end-member fluids at the Von Damm vent field on the Mid-Cayman Rise, where fluid temperatures reach 226°C, provide an exciting opportunity to examine the extent of abiotic carbon transformations in a highly reducing system. Our results indicate multiple sources of carbon compounds in vent fluids at Von Damm. An ultramafic-influenced hydrothermal system located on the Mount Dent oceanic core complex at 2350 m depth, Von Damm vent fluids contain H2, CH4, and C2+ hydrocarbons in high abundance relative to basalt-hosted vent fields, and in similar abundance to other ultramafic-hosted systems, such as Rainbow and Lost City. The CO2 content and isotopic composition in end-member fluids are virtually identical to bottom seawater, suggesting that seawater DIC is unchanged during hydrothermal circulation of seawater-derived fluids. Accordingly, end-member CH4 that is present in slightly greater abundance than CO2 cannot be generated from reduction of aqueous CO2 during hydrothermal circulation. We postulate that CH4 and C2+ hydrocarbons that are abundantly present in Von Damm vent fluids reflect leaching of fluids from carbon- and H2-rich fluid inclusions hosted in plutonic rocks. Geochemical modeling of carbon speciation in the Von Damm fluids suggests that the relative abundances of CH4, C2+ hydrocarbons, and CO2 are consistent with

  1. Organic thin film transistors: from active materials to novel applications

    NASA Astrophysics Data System (ADS)

    Torsi, L.; Cioffi, N.; Di Franco, C.; Sabbatini, L.; Zambonin, P. G.; Bleve-Zacheo, T.

    2001-08-01

    In this paper, a bird's eye view of most of the organic materials employed as n-channel and p-channel transistor active layers is given along with the relevant device performances; organic thin film transistors (OTFT) operation regimes are discussed and an interesting perspective application of OTFT as multi-parameter gas sensor is proposed.

  2. High mobility high efficiency organic films based on pure organic materials

    DOEpatents

    Salzman, Rhonda F.; Forrest, Stephen R.

    2009-01-27

    A method of purifying small molecule organic material, performed as a series of operations beginning with a first sample of the organic small molecule material. The first step is to purify the organic small molecule material by thermal gradient sublimation. The second step is to test the purity of at least one sample from the purified organic small molecule material by spectroscopy. The third step is to repeat the first through third steps on the purified small molecule material if the spectroscopic testing reveals any peaks exceeding a threshold percentage of a magnitude of a characteristic peak of a target organic small molecule. The steps are performed at least twice. The threshold percentage is at most 10%. Preferably the threshold percentage is 5% and more preferably 2%. The threshold percentage may be selected based on the spectra of past samples that achieved target performance characteristics in finished devices.

  3. Organic light emitting device architecture for reducing the number of organic materials

    DOEpatents

    D'Andrade, Brian; Esler, James

    2011-10-18

    An organic light emitting device is provided. The device includes an anode and a cathode. A first emissive layer is disposed between the anode and the cathode. The first emissive layer includes a first non-emitting organic material, which is an organometallic material present in the first emissive layer in a concentration of at least 50 wt %. The first emissive layer also includes a first emitting organic material. A second emissive layer is disposed between the first emissive layer and the cathode, preferably, in direct contact with the first emissive layer. The second emissive material includes a second non-emitting organic material and a second emitting organic material. The first and second non-emitting materials, and the first and second emitting materials, are all different materials. A first non-emissive layer is disposed between the first emissive layer and the anode, and in direct contact with the first emissive layer. The first non- emissive layer comprises the first non-emissive organic material.

  4. New Directions for Organic Spintronics: Novel Materials and Emergent Phenomena

    NASA Astrophysics Data System (ADS)

    Johnston-Halperin, Ezekiel

    Organic and organic-based materials are attractive candidates for applications in magnetoelectronics and spintronics due to their low cost, ease of fabrication, and low spin-orbit coupling (and consequently long spin lifetimes). However, in comparison to the case for inorganic systems, robust intrinsic magnetic ordering in this class of materials is exceedingly rare and as a result the potential of these materials has yet to be fully realized. Here we present a series of recent breakthroughs in the synthesis, encapsulation, and measurement of organic-based magnets that lay the foundation for all organic magnetoelectronic and spintronic devices. We will discuss advances in encapsulation strategies that allow lifetimes of up to 1 month in air for functional magnetoelectronic devices, the use of ligand substitution to generate a library of related magnetic materials, the growth of all-organic and hybrid organic/inorganic magnetic heterostructures, and measurements of the magnetization dynamics that reveal ferromagnetic resonance (FMR) linewidths of ~1 G, comparable to or narrower than corresponding measurements in yttrium iron garnet (YIG). These results establish the validity of organic-based magnets for applications in next-generation magnetoelectronics and provide unique leverage on long-standing challenges in the field of organic spintronics. For example, organic magnetic heterostructures promise to provide an exciting opportunity to explore exchange, dynamic spin injection, and spin transport in all-organic spintronic devices. This work was supported in part by NSF DMR-1507775 and the Center for Emergent Materials (an NSFMRSEC; Award Number DMR-1420451) at The Ohio State University.

  5. Photoconversion of organic materials into single-cell protein

    SciTech Connect

    Weaver, P.F.

    1991-12-31

    A process is described for converting organic materials (such as biomass wastes) into sterile, high-grade bacterial protein suitable for use an animal feed or human food supplements. In a preferred embodiment the process involves thermally gasifying the organic material into primarily carbon monoxide, hydrogen and nitrogen products, followed by photosynthetic bacterial assimilation of the gases into cell material, which can be high as 65% protein. The process is ideally suited for waste recycling and for food production under zero-gravity or extra-terrestrial conditions.

  6. Photoconversion of organic materials into single-cell protein

    DOEpatents

    Weaver, Paul F.

    2001-01-01

    A process is described for converting organic materials (such as biomass wastes) into sterile, high-grade bacterial protein suitable for use an animal feed or human food supplements. In a preferred embodiment the process involves thermally gasifying the organic material into primarily carbon monoxide, hydrogen and nitrogen products, followed by photosynthetic bacterial assimilation of the gases into cell material, which can be as high as 65% protein. The process is ideally suited for waste recycling and for food production under zero-gravity or extra-terrestrial conditions.

  7. Novel solutions for thin film layer deposition for organic materials

    NASA Astrophysics Data System (ADS)

    Keiper, Dietmar; Long, Michael; Schwambera, Markus; Gersdorff, Markus; Kreis, Juergen; Heuken, Michael

    2011-03-01

    Innovative systems for carrier-gas enhanced vapor phase deposition of organic layers offer advanced methods for the precise deposition of complex thin-film layer stacks. The approach inherently avoids potential short-comings from solvent-based polymer deposition and offers new opportunities. The process operates at low pressure (thus avoiding complex vacuum setups), and, by employing AIXTRON's extensive experience in freely scalable solutions, can be adapted to virtually any production process and allows for R&D and production systems alike. Deposition of organic layers and stacks recommends the approach for a wide range of organic small molecule and polymer materials (including layers with gradual change of the composition), for conductive layers, for dielectric layers, for barrier systems, for OLED materials, and surface treatments such as oleophobic / hydrophobic coatings. With the combination of other vapor phase deposition solutions, hybrid systems combining organic and inorganic materials and other advanced stacks can be realized.

  8. Microgravity Processing and Photonic Applications of Organic and Polymeric Materials

    NASA Technical Reports Server (NTRS)

    Frazier, Donald O.; Penn, Benjamin G.; Smith, David D.; Witherow, William K.; Paley, Mark S.; Abdeldayem, Hossin A.

    1997-01-01

    In recent years, a great deal of interest has been directed toward the use of organic materials in the development of high-efficiency optoelectronic and photonic devices. There is a myriad of possibilities among organics which allow flexibility in the design of unique structures with a variety of functional groups. The use of nonlinear optical (NLO) organic materials such as thin-film waveguides allows full exploitation of their desirable qualities by permitting long interaction lengths and large susceptibilities allowing modest power input. There are several methods in use to prepare thin films, such as Langmuir-Blodgett (LB) and self-assembly techniques, vapor deposition, growth from sheared solution or melt, and melt growth between glass plates. Organics have many features that make them desirable for use in optical devices such as high second- and third-order nonlinearities, flexibility of molecular design, and damage resistance to optical radiation. However, their use in devices has been hindered by processing difficulties for crystals and thin films. In this chapter, we discuss photonic and optoelectronic applications of a few organic materials and the potential role of microgravity on processing these materials. It is of interest to note how materials with second- and third-order nonlinear optical behavior may be improved in a diffusion-limited environment and ways in which convection may be detrimental to these materials.

  9. Organic materials and devices for detecting ionizing radiation

    DOEpatents

    Doty, F. Patrick; Chinn, Douglas A.

    2007-03-06

    A .pi.-conjugated organic material for detecting ionizing radiation, and particularly for detecting low energy fission neutrons. The .pi.-conjugated materials comprise a class of organic materials whose members are intrinsic semiconducting materials. Included in this class are .pi.-conjugated polymers, polyaromatic hydrocarbon molecules, and quinolates. Because of their high resistivities (.gtoreq.10.sup.9 ohmcm), these .pi.-conjugated organic materials exhibit very low leakage currents. A device for detecting and measuring ionizing radiation can be made by applying an electric field to a layer of the .pi.-conjugated polymer material to measure electron/hole pair formation. A layer of the .pi.-conjugated polymer material can be made by conventional polymer fabrication methods and can be cast into sheets capable of covering large areas. These sheets of polymer radiation detector material can be deposited between flexible electrodes and rolled up to form a radiation detector occupying a small volume but having a large surface area. The semiconducting polymer material can be easily fabricated in layers about 10 .mu.m to 100 .mu.m thick. These thin polymer layers and their associated electrodes can be stacked to form unique multi-layer detector arrangements that occupy small volume.

  10. An instrument for elemental and isotopic abundance characterization of extra-terrestrial materials

    NASA Astrophysics Data System (ADS)

    Veryovkin, I. V.; Calaway, W. F.; Moore, J. F.; Pellin, M. J.; Savina, M. R.; King, B. V.; Petravić, M.; Burnett, D. S.

    2002-12-01

    prototype instrument and results of recent tests will be presented. This work is supported by the U. S. Department of Energy, BES-Materials Sciences, under Contract W-31-109-ENG-38 and in part by a contract from NASA's Office of Space Science's Cosmochemistry Program.

  11. Microgravity Processing and Photonic Applications of Organic and Polymeric Materials

    NASA Technical Reports Server (NTRS)

    Frazier, Donald 0; Penn, Benjamin G.; Smith, David; Witherow, William K.; Paley, M. S.; Abdeldayem, Hossin A.

    1998-01-01

    In recent years, a great deal of interest has been directed toward the use of organic materials in the development of high-efficiency optoelectronic and photonic devices. There is a myriad of possibilities among organic which allow flexibility in the design of unique structures with a variety of functional groups. The use of nonlinear optical (NLO) organic materials such as thin-film waveguides allows full exploitation of their desirable qualities by permitting long interaction lengths and large susceptibilities allowing modest power input. There are several methods in use to prepare thin films, such as Langmuir-Blodgett (LB) and self-assembly techniques, vapor deposition, growth from sheared solution or melt, and melt growth between glass plates. Organics have many features that make Abstract: them desirable for use in optical devices such as high second- and third-order nonlinearities, flexibility of molecular design, and damage resistance to optical radiation. However, their use in devices has been hindered by processing difficulties for crystals and thin films. In this chapter, we discuss photonic and optoelectronic applications of a few organic materials and the potential role of microgravity on processing these materials. It is of interest to note how materials with second- and third-order nonlinear optical behavior may be improved in a diffusion-limited environment and ways in which convection may be detrimental to these materials. We focus our discussion on third-order materials for all-optical switching, and second-order materials for all-optical switching, and second-order materials for frequency conversion and electrooptics.

  12. Resolving the influence of nitrogen abundances on sediment organic matter in macrophyte-dominated lakes, using fluorescence spectroscopy.

    PubMed

    Yao, Xin; Wang, Shengrui; Jiao, Lixin; Yan, Caihong; Jin, Xiangcan

    2015-01-01

    A controlled experiment was designed to resolve the influence of nitrogen abundance on sediment organic matters in macrophyte-dominated lakes using fluorescence analysis. Macrophyte biomass showed coincident growth trends with time, but different variation rates with nitrogen treatment. All plant growth indexes with nitrogen addition (N, NH4Cl 100, 200, 400mg/kg, respectively) were lower than those of the control group. Four humic-like components, two autochthonous tryptophan-like components, and one autochthonous tyrosine-like component were identified using the parallel factor analysis model. The results suggested that the relative component changes of fluorescence in the colonized sediments were in direct relation to the change of root biomass with time. In the experiment, the root formation parameters of the plants studied were significantly affected by adding N in sediments, which may be related to the reason that the root growth was affected by N addition. Adding a low concentration of N to sediments can play a part in supplying nutrients to the plants. However, the intensive uptake of NH4(+) may result in an increase in the intracellular concentration of ammonia, which is highly toxic to the plant cells. Hence, our experiment results manifested that organic matter cycling in the macrophyte-dominated sediment was influenced by nitrogen enrichment through influencing vegetation and relevant microbial activity. PMID:25597678

  13. Conducting Polymers and Their Hybrids as Organic Thermoelectric Materials

    NASA Astrophysics Data System (ADS)

    Toshima, Naoki; Ichikawa, Shoko

    2015-01-01

    Conducting polymers have received much attention recently as organic thermoelectric materials, because of such advantages as plentiful resources, easy synthesis, easy processing, low cost, low thermal conductivity, and easy fabrication of flexible, light, and printable devices with large area. Many reports on organic thermoelectric materials have recently been published. We have studied conducting polymers as organic thermoelectric materials since 1999. During these investigations, we found that the thermal conductivity of conducting polymers did not increase even though electrical conductivity increased; this was a major advantage of conducting polymers as organic thermoelectric materials. We also observed that molecular alignment was one of the most important factors for improvement of the thermoelectric performance of conducting polymers. Stretching of conducting polymers or their precursors was one of the most common techniques used to achieve good molecular alignment. Recently, alignment of the clusters of conducting polymers by treatment with solvents has been proposed as a means of achieving high electrical conductivity. Hybridization of conducting polymers with inorganic nanoparticles has also been found to improve thermoelectric performance. Here we present a brief history and discuss recent progress of research on conducting polymers as organic thermoelectric materials, and describe the techniques used to improve thermoelectric performance by treatment of conducting polymers with solvents and hybridization of conducting polymers with Bi2Te3 and gold nanoparticles.

  14. Organic materials for second harmonic generation. Final report

    SciTech Connect

    Twieg, R.J.

    1985-03-31

    Materials were chosen by screening the Cambridge Crystallographic Index for new noncentrosymmetric crystalline compounds, by screening commercially available materials or by synthesis of unique new substances. Measurements were then made on the powder form of these materials. Langmuir-Blodgett films were deposited and studied. In addition to the above studies, a computer program was developed to calculate (hyper) polarizabilities of organic molecules and thus aid in the selection of materials for testing. The nonlinear molecules have been divided into three classes according to absorption cutoff: 400 to 500 nm, 300 to 400 nm, and 200 to 300 nm. 108 refs., 7 tabs. (WRF)

  15. New organic-inorganic hybrid molecular systems and highly organized materials in catalysis

    NASA Astrophysics Data System (ADS)

    Kustov, L. M.

    2015-11-01

    Definitions of hybrid materials are suggested, and applications of these materials are considered. Particular attention is focused on the application of hybrid materials in hydrogenation, partial oxidation, plant biomass conversion, and natural gas reforming, primarily on the use of core-shell nanoparticles and decorated metal nanoparticles in these reactions. Application prospects of various hybrid materials, particularly those of metal-organic frameworks, are discussed.

  16. Thermal Desorption/GCMS Analysis of Astrobiologically Relevant Organic Materials

    NASA Technical Reports Server (NTRS)

    McDonald, Gene D.

    2001-01-01

    Several macromolecular organic materials, both biologically-derived (type II kerogen and humic acid) and abiotic in origin (Murchison insoluble organic material, cyanide polymer, and Titan tholin) were subjected to thermal desorption using a Chromatoprobe attachment on a Varian Saturn 2000 GCMS system. Each sample was heated sequentially at 100, 200, and 300 C to release volatile components. The evolved compounds were then separated on a Supelco EC-1 dimethylsilica GC column and detected by the Saturn 2000 ion trap mass spectrometer. The various types of macromolecular organic material subjected to thermal desorption produced distinctly different GCMS chromatograms at each temperature, containing fractions of both low and high chromatographic mobility. The relative amounts of detectable volatiles released at each temperature also differed, with type II kerogen and cyanide polymer containing the highest percentage of low-temperature components. In all the samples, the highest yield of released compounds occurred at 300 C. Only cyanide polymer evolved a homologous hydrocarbon series, suggesting that it is the only material among those examined that contains a truly polymeric structure. Pyrolysis/gas chromatography/mass spectrometry has been used extensively for analysis of terrestrial organic macromolecular materials, and was also part of the instrument package on the Viking landers. Thorough analysis by pyrolysis usually employs temperatures of 500 C or higher, which for in situ analyses can be problematic given spacecraft power and materials constraints. This study demonstrates that heating of organic materials of astrobiological relevance to temperatures as low as 200-300 C for short periods releases volatile components that can be analyzed by gas chromatography and mass spectrometry. Even in the absence of full pyrolysis, useful chemical information on samples can be obtained, and materials from different biological and abiological sources can be distinguished

  17. Effect of natural organic materials on cadmium and neptunium sorption

    SciTech Connect

    Kung, K.S.; Triay, I.R.

    1994-10-01

    In a batch sorption study of the effect of naturally occurring organic materials on the sorption of cadmium and neptunium on oxides and tuff surfaces, the model sorbents were synthetic goethite, boehmite, amorphous silicon oxides, and a crushed tuff material from Yucca Mountain, Nevada. An amino acid, 3-(3,4-dihydroxypheny)-DL-alanine (DOPA), and an aquatic-originated fulvic material, Nordic aquatic fulvic acid (NAFA), were used as model organic chemicals. Sorption isotherm results showed that DOPA sorption followed the order aluminum oxide > iron oxide > silicon oxide and that the amount of DOAP sorption for a given sorbent increased as the solution pH was raised. The sorption of cadmium and neptunium on the iron oxide was about ten times higher than that on the aluminum oxide. The sorption of cadmium and neptunium on natural tuff material was much lower than that on aluminum and iron oxides. The sorption of cadmium on iron and aluminum oxides was found to be influenced by the presence of DOPA, and increasing the amount of DOPA coating resulted in higher cadmium sorption on aluminum oxide. However, for iron oxide, cadmium sorption decreased with increasing DOPA concentration. The presence of the model organic materials DOPA and NAFA did not affect the sorption of neptunium on tuff material or on the iron and aluminum oxides. Spectroscopic results indicate that cadmium complexes strongly with DOPA. Therefore, the effect of the organic material, DOPA, on the cadmium sorption is readily observed. However, neptunium is possibly complexed weakly with organic material. Thus, DOPA and NAFA have little effect on neptunium sorption on all sorbents selected for study.

  18. Chronic hypoxia and VEGF differentially modulate abundance and organization of myosin heavy chain isoforms in fetal and adult ovine arteries.

    PubMed

    Hubbell, Margaret C; Semotiuk, Andrew J; Thorpe, Richard B; Adeoye, Olayemi O; Butler, Stacy M; Williams, James M; Khorram, Omid; Pearce, William J

    2012-11-15

    Chronic hypoxia increases vascular endothelial growth factor (VEGF) and thereby promotes angiogenesis. The present study explores the hypothesis that hypoxic increases in VEGF also remodel artery wall structure and contractility through phenotypic transformation of smooth muscle. Pregnant and nonpregnant ewes were maintained at sea level (normoxia) or 3,820 m (hypoxia) for the final 110 days of gestation. Common carotid arteries harvested from term fetal lambs and nonpregnant adults were denuded of endothelium and studied in vitro. Stretch-dependent contractile stresses were 32 and 77% of normoxic values in hypoxic fetal and adult arteries. Hypoxic hypocontractility was coupled with increased abundance of nonmuscle myosin heavy chain (NM-MHC) in fetal (+37%) and adult (+119%) arteries. Conversely, hypoxia decreased smooth muscle MHC (SM-MHC) abundance by 40% in fetal arteries but increased it 123% in adult arteries. Hypoxia decreased colocalization of NM-MHC with smooth muscle α-actin (SM-αA) in fetal arteries and decreased colocalization of SM-MHC with SM-αA in adult arteries. Organ culture with physiological concentrations (3 ng/ml) of VEGF-A(165) similarly depressed stretch-dependent stresses to 37 and 49% of control fetal and adult values. The VEGF receptor antagonist vatalanib ablated VEGF's effects in adult but not fetal arteries, suggesting age-dependent VEGF receptor signaling. VEGF replicated hypoxic decreases in colocalization of NM-MHC with SM-αA in fetal arteries and decreases in colocalization of SM-MHC with SM-αA in adult arteries. These results suggest that hypoxic increases in VEGF not only promote angiogenesis but may also help mediate hypoxic arterial remodeling through age-dependent changes in smooth muscle phenotype and contractility. PMID:22992677

  19. Low abundance materials at the mars pathfinder landing site: An investigation using spectral mixture analysis and related techniques

    USGS Publications Warehouse

    Bell, J.F., III; Farrand, W. H.; Johnson, J. R.; Morris, R.V.

    2002-01-01

    Recalibrated and geometrically registered multispectral images from the Imager for Mars Pathfinder (IMP) were analyzed using Spectral Mixture Analysis (SMA) and related techniques. SMA models a multispectral image scene as a linear combination of end-member spectra, and anomalous materials which do not fit the model are detected as model residuals. While most of the IMP data studied here are modeled generally well using "Bright Dust," "Gray Rock," and "Shade" image endmembers, additional anomalous materials were detected through careful analysis of root mean square (RMS) error images resulting from SMA. For example, analysis of SMA fraction and RMS images indicates spectral differences within a previously monolithologic Dark Soil class. A type of Dark Soil that has high fractional abundances in rock fraction images (Gray Rock Soil) was identified. Other anomalous materials identified included a previously noted "Black Rock" lithology, a class of possibly indurated, compacted, or partially cemented soils ("Intermediate Soil"), and a unit referred to as "Anomalous Patches" on at least one rock. The Black Rock lithology has a strong 900-1000-nm absorption, and modeling of the derived image endmembers using a laboratory reference endmember modeling (REM) approach produced best-fit model spectra that are most consistent with the presence of high-Ca pyroxenes and/or olivine, crystalline ferric oxide minerals, or mixtures of these materials as important components of the Black Rock endmember. More unique mineralogic identifications could not be obtained using our initial REM analyses. Both Intermediate Soil and Anomalous Patches units exhibit a relatively narrow 860-950-nm absorption that is consistent with the presence of either low-Ca pyroxenes or a cementing crystalline ferric oxide mineral. ?? 2002 Elsevier Science (USA).

  20. Advanced organic composite materials for aircraft structures: Future program

    NASA Technical Reports Server (NTRS)

    1987-01-01

    Revolutionary advances in structural materials have been responsible for revolutionary changes in all fields of engineering. These advances have had and are still having a significant impact on aircraft design and performance. Composites are engineered materials. Their properties are tailored through the use of a mix or blend of different constituents to maximize selected properties of strength and/or stiffness at reduced weights. More than 20 years have passed since the potentials of filamentary composite materials were identified. During the 1970s much lower cost carbon filaments became a reality and gradually designers turned from boron to carbon composites. Despite progress in this field, filamentary composites still have significant unfulfilled potential for increasing aircraft productivity; the rendering of advanced organic composite materials into production aircraft structures was disappointingly slow. Why this is and research and technology development actions that will assist in accelerating the application of advanced organic composites to production aircraft is discussed.

  1. Minerals yearbook, 1991: Nonrenewable organic materials. Annual report

    SciTech Connect

    Simmons, M.R.; Kelly, T.D.

    1993-05-01

    Mrs. Simmons, industrial program manager with the Branch of Materials of the U.S. Bureau of Mines, directs work in the analysis of the petroleum, petrochemical, and plastic industries as related to the application of nonrenewable organic materials in major industrial sectors. Mr. Kelly, materials specialist in the Materials Engineering Group at the Minerals Availability Office of the U.S. Bureau of Mines, has over 6 years of experience in the petroleum industry. Some of the data were prepared by John Sznopeke, materials specialist in the Materials Engineering Group at the Minerals Availability Field Office. The data were obtained from a variety of sources, including the Annual Energy Review 1991 from the Energy Information Administration, U.S. Department of Energy; the Department of Commerce; and a wide variety of industry contacts.

  2. Highly Non-Linear Optical (NLO) organic crystals and films. Electrooptical organic materials

    NASA Technical Reports Server (NTRS)

    Mcmanus, Samuel P.; Rosenberger, Franz; Matthews, John

    1987-01-01

    Devices employing nonlinear optics (NLO) hold great promise for important applications in integrated optics, optical information processing and telecommunications. Properly designed organics possess outstanding optical and electrooptical properties which will substantially advance many technologies including electrooptical switching, optical amplification for communications, and parallel processing for hybrid optical computers. A brief comparison of organic and inorganic materials is given.

  3. Nonlinear optical properties of organic materials: A theoretical study

    NASA Technical Reports Server (NTRS)

    Cardelino, Beatriz H.

    1991-01-01

    Replacement of electronic switching circuits in computing and telecommunication systems with purely optical devices offers the potential for extremely high throughput and compact information processing systems. The potential application of organic materials containing molecules with large nonresonant nonlinear effects in this area have triggered intensive research during the last decade. Interest on this area was due to two facts: (1) that many organic materials show nonlinearities that are orders of magnitude larger than those of conventional inorganic materials such as lithium niobate and potassium dihydrogen phosphate; and (2) that organic materials show much flexibility in terms of molecular designs. Some of the desirable characteristics that these materials should have are that they be transparent to the frequency of the incident laser and its second or third harmonic, that they have a high damage threshold, and, in the case of second-order effects, that their crystal structure or molecular orientation be accentric. Since polymeric assemblages can enhance the nonlinear response of organic molecules severalfold, efforts have been directed toward the synthesis of thin films with interpenetrating lattices of electroactive molecules. The goal of this theoretical investigation is to predict the magnitude of the molecular polarizabilities of organic molecules that could be incorporated into films. These calculations are intended to become a powerful tool to assist material scientists in screening for the best candidates for optical applications. The procedure that was developed for the present calculations is based on the static-field approach, and is a modification to the method developed by Dewar and Stewart, 1984 for calculating molecular linear polarizabilities.

  4. "Candidatus Propionivibrio aalborgensis": A Novel Glycogen Accumulating Organism Abundant in Full-Scale Enhanced Biological Phosphorus Removal Plants.

    PubMed

    Albertsen, Mads; McIlroy, Simon J; Stokholm-Bjerregaard, Mikkel; Karst, Søren M; Nielsen, Per H

    2016-01-01

    Enhanced biological phosphorus removal (EBPR) is widely used to remove phosphorus from wastewater. The process relies on polyphosphate accumulating organisms (PAOs) that are able to take up phosphorus in excess of what is needed for growth, whereby phosphorus can be removed from the wastewater by wasting the biomass. However, glycogen accumulating organisms (GAOs) may reduce the EBPR efficiency as they compete for substrates with PAOs, but do not store excessive amounts of polyphosphate. PAOs and GAOs are thought to be phylogenetically unrelated, with the model PAO being the betaproteobacterial "Candidatus Accumulibacter phosphatis" (Accumulibacter) and the model GAO being the gammaproteobacterial "Candidatus Competibacter phosphatis". Here, we report the discovery of a GAO from the genus Propionivibrio, which is closely related to Accumulibacter. Propionivibrio sp. are targeted by the canonical fluorescence in situ hybridization probes used to target Accumulibacter (PAOmix), but do not store excessive amounts of polyphosphate in situ. A laboratory scale reactor, operated to enrich for PAOs, surprisingly contained co-dominant populations of Propionivibrio and Accumulibacter. Metagenomic sequencing of multiple time-points enabled recovery of near complete population genomes from both genera. Annotation of the Propionivibrio genome confirmed their potential for the GAO phenotype and a basic metabolic model is proposed for their metabolism in the EBPR environment. Using newly designed fluorescence in situ hybridization (FISH) probes, analyses of full-scale EBPR plants revealed that Propionivibrio is a common member of the community, constituting up to 3% of the biovolume. To avoid overestimation of Accumulibacter abundance in situ, we recommend the use of the FISH probe PAO651 instead of the commonly applied PAOmix probe set. PMID:27458436

  5. “Candidatus Propionivibrio aalborgensis”: A Novel Glycogen Accumulating Organism Abundant in Full-Scale Enhanced Biological Phosphorus Removal Plants

    PubMed Central

    Albertsen, Mads; McIlroy, Simon J.; Stokholm-Bjerregaard, Mikkel; Karst, Søren M.; Nielsen, Per H.

    2016-01-01

    Enhanced biological phosphorus removal (EBPR) is widely used to remove phosphorus from wastewater. The process relies on polyphosphate accumulating organisms (PAOs) that are able to take up phosphorus in excess of what is needed for growth, whereby phosphorus can be removed from the wastewater by wasting the biomass. However, glycogen accumulating organisms (GAOs) may reduce the EBPR efficiency as they compete for substrates with PAOs, but do not store excessive amounts of polyphosphate. PAOs and GAOs are thought to be phylogenetically unrelated, with the model PAO being the betaproteobacterial “Candidatus Accumulibacter phosphatis” (Accumulibacter) and the model GAO being the gammaproteobacterial “Candidatus Competibacter phosphatis”. Here, we report the discovery of a GAO from the genus Propionivibrio, which is closely related to Accumulibacter. Propionivibrio sp. are targeted by the canonical fluorescence in situ hybridization probes used to target Accumulibacter (PAOmix), but do not store excessive amounts of polyphosphate in situ. A laboratory scale reactor, operated to enrich for PAOs, surprisingly contained co-dominant populations of Propionivibrio and Accumulibacter. Metagenomic sequencing of multiple time-points enabled recovery of near complete population genomes from both genera. Annotation of the Propionivibrio genome confirmed their potential for the GAO phenotype and a basic metabolic model is proposed for their metabolism in the EBPR environment. Using newly designed fluorescence in situ hybridization (FISH) probes, analyses of full-scale EBPR plants revealed that Propionivibrio is a common member of the community, constituting up to 3% of the biovolume. To avoid overestimation of Accumulibacter abundance in situ, we recommend the use of the FISH probe PAO651 instead of the commonly applied PAOmix probe set. PMID:27458436

  6. Variability in the bulk composition and abundance of dissolved organic matter in the lower Mississippi and Pearl rivers

    NASA Astrophysics Data System (ADS)

    Duan, Shuiwang; Bianchi, Thomas S.; Shiller, Alan M.; Dria, Karl; Hatcher, Patrick G.; Carman, Kevin R.

    2007-06-01

    In this study, we examined the temporal and spatial variability of dissolved organic matter (DOM) abundance and composition in the lower Mississippi and Pearl rivers and effects of human and natural influences. In particular, we looked at bulk C/N ratio, stable isotopes (δ15N and δ13C) and 13C nuclear magnetic resonance (NMR) spectrometry of high molecular weight (HMW; 0.2 μm to 1 kDa) DOM. Monthly water samples were collected at one station in each river from August 2001 to 2003. Surveys of spatial variability of total dissolved organic carbon (DOC) and nitrogen (DON) were also conducted in June 2003, from 390 km downstream in the Mississippi River and from Jackson to Stennis Space Center in the Pearl River. Higher DOC (336-1170 μM), C/N ratio,% aromaticity, and more depleted δ15N (0.76-2.1‰) were observed in the Pearl than in the lower Mississippi River (223-380 μM, 4.7-11.5‰, respectively). DOC, C/N ratio, δ13C, δ15N, and % aromaticity of Pearl River HMW DOM were correlated with water discharge, which indicated a coupling between local soil inputs and regional precipitation events. Conversely, seasonal variability in the lower Mississippi River was more controlled by spatial variability of a larger integrative signal from the watershed as well as in situ DOM processing. Spatially, very little change occurred in total DOC in the downstream survey of the lower Mississippi River, compared to a decrease of 24% in the Pearl River. Differences in DOM between these two rivers were reflective of the Mississippi River having more extensive river processing of terrestrial DOM, more phytoplankton inputs, and greater anthropogenic perturbation than the Pearl River.

  7. Information Identification and Organization. Student Study Guide. Module II: Organization and Acquisition of Information and Materials.

    ERIC Educational Resources Information Center

    Bolvin, Boyd M.; West, Sharon

    This second module in a three module program examines the types of materials and services that are available in a community information center or library and the tools or sources for obtaining them. The module covers: ways in which books and other materials are arranged and organized; descriptions of library catalogs and the basic information…

  8. MODELING THE FATE OF TOXIC ORGANIC MATERIALS IN AQUATIC ENVIRONMENTS

    EPA Science Inventory

    Documentation is given for PEST, a dynamic simulation model for evaluating the fate of toxic organic materials (TOM) in freshwater environments. PEST represents the time-varying concentration (in ppm) of a given TOM in each of as many as 16 carrier compartments; it also computes ...

  9. CHARACTERIZATION OF ORGANIC EMISSIONS FROM SELECTED MATERIALS IN INDOOR USE

    EPA Science Inventory

    The paper provides data from small-chamber testing of a latex caulk and a floor adhesive, as part of EPA's ongoing evaluation of organic emissions from indoor materials. Among the conclusions drawn from presented data are: (1) low air exchange rates promote high concentrations of...

  10. Organic/inorganic hybrid materials: challenges for ab initio methodology.

    PubMed

    Draxl, Claudia; Nabok, Dmitrii; Hannewald, Karsten

    2014-11-18

    CONSPECTUS: Organic/inorganic hybrid structures are most exciting since one can expect new properties that are absent in either of their building blocks. They open new perspectives toward the design and tailoring of materials with desired features and functions. Prerequisite for real progress is, however, the in-depth understanding of what happens on the atomic and electronic scale. In this respect, hybrid materials pose a challenge for electronic-structure theory. Methods that proved useful for describing one side may not be applicable for the other one, and they are likely to fail for the interfaces. In this Account, we address the question to what extent we can quantitatively describe hybrid materials and where we even miss a qualitative description. We note that we are dealing with extended systems and thus adopt a solid-state approach. Therefore, density-functional theory (DFT) and many-body perturbation theory (MBPT), the GW approach for charged and the Bethe-Salpeter equation for neutral excitations, are our methods of choice. We give a brief summary of the used methodology, focusing on those aspects where problems can be expected when materials of different character meet at an interface. These issues are then taken up when discussing hybrid materials. We argue when and why, for example, standard DFT may fall short when it comes to the electronic structure of organic/metal interfaces or where the framework of MBPT can or must take over. Selected examples of organic/inorganic interfaces, structural properties, electronic bands, optical excitation spectra, and charge-transport properties as obtained from DFT and MBPT highlight which properties can be reliably computed for such materials. The crucial role of van der Waals forces is shown for sexiphenyl films, where the subtle interplay between intermolecular and molecule-substrate interactions is decisive for growth and morphologies. With a PTCDA monolayer on metal surfaces we discuss the performance of DFT in

  11. Quantifying singlet fission in novel organic materials using nonlinear optics

    NASA Astrophysics Data System (ADS)

    Busby, Erik; Xia, Jianlong; Yaffe, Omer; Kumar, Bharat; Berkelbach, Timothy; Wu, Qin; Miller, John; Nuckolls, Colin; Zhu, Xiaoyang; Reichman, David; Campos, Luis; Sfeir, Matthew Y.

    2014-10-01

    Singlet fission is a form of multiple exciton generation in which two triplet excitons are produced from the decay of a photoexcited singlet exciton. In a small number of organic materials, most notably pentacene, this conversion process has been shown to occur with unity quantum yield on sub-ps timescales. However, a poorly understood mechanism for fission along with strict energy and geometry requirements have so far limited the observation of this process to a few classes of organic materials, with only a subset of these (most notably the polyacenes) showing both efficient fission and long-lived triplets. Here, we utilize novel organic materials to investigate how the efficiency of the fission process depends on the coupling and the energetic driving force between chromophores in both intra- and intermolecular singlet fission materials. We demonstrate how the triplet yield can be accurately quantified using a combination of traditional transient spectroscopies and recently developed excited state saturable absorption techniques. These results allow us to gain mechanistic insight into the fission process and suggest general strategies for generating new materials that can undergo efficient fission.

  12. Self-organization of functional materials in confinement.

    PubMed

    Gentili, Denis; Valle, Francesco; Albonetti, Cristiano; Liscio, Fabiola; Cavallini, Massimiliano

    2014-08-19

    This Account aims to describe our experience in the use of patterning techniques for addressing the self-organization processes of materials into spatially confined regions on technologically relevant surfaces. Functional properties of materials depend on their chemical structure, their assembly, and spatial distribution at the solid state; the combination of these factors determines their properties and their technological applications. In fact, by controlling the assembly processes and the spatial distribution of the resulting structures, functional materials can be guided to technological and specific applications. We considered the principal self-organizing processes, such as crystallization, dewetting and phase segregation. Usually, these phenomena produce defective molecular films, compromising their use in many technological applications. This issue can be overcome by using patterning techniques, which induce molecules to self-organize into well-defined patterned structures, by means of spatial confinement. In particular, we focus our attention on the confinement effect achieved by stamp-assisted deposition for controlling size, density, and positions of material assemblies, giving them new chemical/physical functionalities. We review the methods and principles of the stamp-assisted spatial confinement and we discuss how they can be advantageously exploited to control crystalline order/orientation, dewetting phenomena, and spontaneous phase segregation. Moreover, we highlight how physical/chemical properties of soluble functional materials can be driven in constructive ways, by integrating them into operating technological devices. PMID:25068634

  13. Vinasse organic matter quality and mineralization potential, as influenced by raw material, fermentation and concentration processes.

    PubMed

    Parnaudeau, V; Condom, N; Oliver, R; Cazevieille, P; Recous, S

    2008-04-01

    Both dilute and concentrated vinasse can be spread on agricultural fields or used as organic fertilizer. The effects of different characteristics of the original raw material on the biochemical composition of vinasse and their C and N mineralization in soil were investigated. Vinasse samples were obtained from similar industrial fermentation processes based on the growth of microorganisms on molasses from different raw material (sugar beet or sugar cane) and vinasse concentration (dilute or concentrated). The nature of the raw material used for fermentation had the greatest effect on the nature and size of the resistant organic pool. This fraction included aromatic compounds originating from the raw material or from complex molecules and seemed to be quantitatively related to acid-insoluble N. Samples derived from sugar beet were richer in N compounds and induced greater net N mineralization. The effect of evaporation varied with the nature of the raw material. Concentration led to a slight increase in the abundance of phenolic compounds, acid-insoluble fraction, and a slight decrease in the labile fraction of vinasses partly or totally derived from sugar beet. The effect of the dilute vinasse from sugar cane was greater. The concentrated vinasse had a smaller labile fraction, induced N immobilization at the beginning of incubation, and exhibited greater N concentration in the acid-insoluble fraction than the dilute vinasse. PMID:17582760

  14. The polymer-like organic material in the Orgueil meteorite

    NASA Technical Reports Server (NTRS)

    Bandurski, E. L.; Nagy, B.

    1976-01-01

    Results are reported for analysis of polymeric organic material contained in powder from the Orgueil chondrite, using a stepwise high-vacuum pyrolysis-gas chromatography-mass spectrometry technique. Pyrolysis products obtained include a series of alkanes and alkenes to C8, an extensive series of alkylbenzene isomers, thiophene, alkylthiophenes, benzothiophene, acetonitrile, acrylonitrile, benzonitrile, acetone, and phenol. Most of these products are shown to be similar both qualitatively and quantitatively to those previously obtained from solvent-extracted Allende powder, indicating a basically aromatic and heteroaromatic polymer matrix with short aliphatic bridges or side chains. The production of acrylonitrile, acetonitrile, and benzonitrile (common breakdown products of amino acids) from the insoluble organic material is taken to suggest that amino acids exist in an insoluble form, perhaps as peptides, in the meteorite's polymeric component. Similarities between the structure of the Orgueil polymeric material and terrestrial kerogen are discussed which raise the possibility that both might have been produced in part by similar reactions.

  15. Light-emitting device with organic electroluminescent material and photoluminescent materials

    DOEpatents

    McNulty, Thomas Francis; Duggal, Anil Raj; Turner, Larry Gene; Shiang, Joseph John

    2005-06-07

    A light-emitting device comprises a light-emitting member, which comprises two electrodes and an organic electroluminescent material disposed between the electrodes, and at least one organic photoluminescent ("PL") material. The light-emitting member emits light having a first spectrum in response to a voltage applied across the two electrodes. The organic PL material absorbs a portion of the light emitted by the light-emitting member and emits light having second spectrum different than the first spectrum. The light-emitting device can include an inorganic PL material that absorbs another portion of the light emitted from the light-emitting member and emits light having a third spectrum different than both the first and the second spectra.

  16. Mesoscale molecular network formation in amorphous organic materials

    PubMed Central

    Savoie, Brett M.; Kohlstedt, Kevin L.; Jackson, Nicholas E.; Chen, Lin X.; Olvera de la Cruz, Monica; Schatz, George C.; Marks, Tobin J.; Ratner, Mark A.

    2014-01-01

    High-performance solution-processed organic semiconductors maintain macroscopic functionality even in the presence of microscopic disorder. Here we show that the functional robustness of certain organic materials arises from the ability of molecules to create connected mesoscopic electrical networks, even in the absence of periodic order. The hierarchical network structures of two families of important organic photovoltaic acceptors, functionalized fullerenes and perylene diimides, are analyzed using a newly developed graph methodology. The results establish a connection between network robustness and molecular topology, and also demonstrate that solubilizing moieties play a large role in disrupting the molecular networks responsible for charge transport. A clear link is established between the success of mono and bis functionalized fullerene acceptors in organic photovoltaics and their ability to construct mesoscopically connected electrical networks over length scales of 10 nm. PMID:24982179

  17. Isotopic characterisation of prebiotic synthesis of organic material

    NASA Technical Reports Server (NTRS)

    Kerridge, J. F.; Chang, S.

    1986-01-01

    Many primitive meteorites contain an insoluble organic material, much like terrestrial kerogen, whose mode of origin is currently unknown. When sujbected to stepwise decomposition, this material, unlike its terrestrial counterpart, reveals characteristic release patterns for the stable isotopes of carbon, hydrogen and nitrogen as a function of fractional release of each element. The purpose of this study is to try to match those release patterns using organic matter synthesised in the laboratory under controlled conditions. If successful, such a study would shed light on the origin of kerogen-like organic matter in the early solar system and, by extension, on prebiotic organic synthesis in general. The range of possible syntheses, starting materials and reaction conditions to be investigated is considerable. Samples analysed to date include: a heavy oil produced by Fischer-Tropsch-type catalysis of CO + H2; a solid residue generated by a plasma discharge in CO + H2 + N2; a solid deposited on the electrodes of a Miller-Urey synthesis operating on CH4 + H2O + N2; and a solid residue formed by polymerization of light hydrocarbons procured by a Miller-Urey discharge acting on CH4. Significant structure is observed in the release patterns for the carbon and hydrogen isotopes from the synthetic samples, though there is little evidence for isotopic fractionation during the analysis itself.

  18. Classification of organic and biological materials with deep ultraviolet excitation.

    PubMed

    Bhartia, Rohit; Hug, Willam F; Salas, Everett C; Reid, Ray D; Sijapati, Kripa K; Tsapin, Alexandre; Abbey, William; Nealson, Kenneth H; Lane, Arthur L; Conrad, Pamela G

    2008-10-01

    We show that native fluorescence can be used to differentiate classes or groups of organic molecules and biological materials when excitation occurs at specific excitation wavelengths in the deep ultraviolet (UV) region. Native fluorescence excitation-emission maps (EEMs) of pure organic materials, microbiological samples, and environmental background materials were compared using excitation wavelengths between 200-400 nm with emission wavelengths from 270 to 500 nm. These samples included polycyclic aromatic hydrocarbons (PAHs), nitrogen- and sulfur-bearing organic heterocycles, bacterial spores, and bacterial vegetative whole cells (both Gram positive and Gram negative). Each sample was categorized into ten distinct groups based on fluorescence properties. Emission spectra at each of 40 excitation wavelengths were analyzed using principal component analysis (PCA). Optimum excitation wavelengths for differentiating groups were determined using two metrics. We show that deep UV excitation at 235 (+/-2) nm optimally separates all organic and biological groups within our dataset with >90% confidence. For the specific case of separation of bacterial spores from all other samples in the database, excitation at wavelengths less than 250 nm provides maximum separation with >6sigma confidence. PMID:18926014

  19. Purely organic electroluminescent material realizing 100% conversion from electricity to light

    PubMed Central

    Kaji, Hironori; Suzuki, Hajime; Fukushima, Tatsuya; Shizu, Katsuyuki; Suzuki, Katsuaki; Kubo, Shosei; Komino, Takeshi; Oiwa, Hajime; Suzuki, Furitsu; Wakamiya, Atsushi; Murata, Yasujiro; Adachi, Chihaya

    2015-01-01

    Efficient organic light-emitting diodes have been developed using emitters containing rare metals, such as platinum and iridium complexes. However, there is an urgent need to develop emitters composed of more abundant materials. Here we show a thermally activated delayed fluorescence material for organic light-emitting diodes, which realizes both approximately 100% photoluminescence quantum yield and approximately 100% up-conversion of the triplet to singlet excited state. The material contains electron-donating diphenylaminocarbazole and electron-accepting triphenyltriazine moieties. The typical trade-off between effective emission and triplet-to-singlet up-conversion is overcome by fine-tuning the highest occupied molecular orbital and lowest unoccupied molecular orbital distributions. The nearly zero singlet–triplet energy gap, smaller than the thermal energy at room temperature, results in an organic light-emitting diode with external quantum efficiency of 29.6%. An external quantum efficiency of 41.5% is obtained when using an out-coupling sheet. The external quantum efficiency is 30.7% even at a high luminance of 3,000 cd m−2. PMID:26477390

  20. Purely organic electroluminescent material realizing 100% conversion from electricity to light.

    PubMed

    Kaji, Hironori; Suzuki, Hajime; Fukushima, Tatsuya; Shizu, Katsuyuki; Suzuki, Katsuaki; Kubo, Shosei; Komino, Takeshi; Oiwa, Hajime; Suzuki, Furitsu; Wakamiya, Atsushi; Murata, Yasujiro; Adachi, Chihaya

    2015-01-01

    Efficient organic light-emitting diodes have been developed using emitters containing rare metals, such as platinum and iridium complexes. However, there is an urgent need to develop emitters composed of more abundant materials. Here we show a thermally activated delayed fluorescence material for organic light-emitting diodes, which realizes both approximately 100% photoluminescence quantum yield and approximately 100% up-conversion of the triplet to singlet excited state. The material contains electron-donating diphenylaminocarbazole and electron-accepting triphenyltriazine moieties. The typical trade-off between effective emission and triplet-to-singlet up-conversion is overcome by fine-tuning the highest occupied molecular orbital and lowest unoccupied molecular orbital distributions. The nearly zero singlet-triplet energy gap, smaller than the thermal energy at room temperature, results in an organic light-emitting diode with external quantum efficiency of 29.6%. An external quantum efficiency of 41.5% is obtained when using an out-coupling sheet. The external quantum efficiency is 30.7% even at a high luminance of 3,000 cd m(-2). PMID:26477390

  1. Purely organic electroluminescent material realizing 100% conversion from electricity to light

    NASA Astrophysics Data System (ADS)

    Kaji, Hironori; Suzuki, Hajime; Fukushima, Tatsuya; Shizu, Katsuyuki; Suzuki, Katsuaki; Kubo, Shosei; Komino, Takeshi; Oiwa, Hajime; Suzuki, Furitsu; Wakamiya, Atsushi; Murata, Yasujiro; Adachi, Chihaya

    2015-10-01

    Efficient organic light-emitting diodes have been developed using emitters containing rare metals, such as platinum and iridium complexes. However, there is an urgent need to develop emitters composed of more abundant materials. Here we show a thermally activated delayed fluorescence material for organic light-emitting diodes, which realizes both approximately 100% photoluminescence quantum yield and approximately 100% up-conversion of the triplet to singlet excited state. The material contains electron-donating diphenylaminocarbazole and electron-accepting triphenyltriazine moieties. The typical trade-off between effective emission and triplet-to-singlet up-conversion is overcome by fine-tuning the highest occupied molecular orbital and lowest unoccupied molecular orbital distributions. The nearly zero singlet-triplet energy gap, smaller than the thermal energy at room temperature, results in an organic light-emitting diode with external quantum efficiency of 29.6%. An external quantum efficiency of 41.5% is obtained when using an out-coupling sheet. The external quantum efficiency is 30.7% even at a high luminance of 3,000 cd m-2.

  2. Terracidiphilus gabretensis gen. nov., sp. nov., an Abundant and Active Forest Soil Acidobacterium Important in Organic Matter Transformation

    PubMed Central

    García-Fraile, Paula; Benada, Oldrich; Cajthaml, Tomáš; Baldrian, Petr

    2015-01-01

    Understanding the activity of bacteria in coniferous forests is highly important, due to the role of these environments as a global carbon sink. In a study of the microbial biodiversity of montane coniferous forest soil in the Bohemian Forest National Park (Czech Republic), we succeeded in isolating bacterial strain S55T, which belongs to one of the most abundant operational taxonomic units (OTUs) in active bacterial populations, according to the analysis of RNA-derived 16S rRNA amplicons. The 16S rRNA gene sequence analysis showed that the species most closely related to strain S55T include Bryocella elongata SN10T (95.4% identity), Acidicapsa ligni WH120T (95.2% identity), and Telmatobacter bradus TPB6017T (95.0% identity), revealing that strain S55T should be classified within the phylum Acidobacteria, subdivision 1. Strain S55T is a rod-like bacterium that grows at acidic pH (3 to 6). Its phylogenetic, genotypic, phenotypic, and chemotaxonomic characteristics indicate that strain S55T corresponds to a new genus within the phylum Acidobacteria; thus, we propose the name Terracidiphilus gabretensis gen. nov., sp. nov. (strain S55T = NBRC 111238T = CECT 8791T). This strain produces extracellular enzymes implicated in the degradation of plant-derived biopolymers. Moreover, analysis of the genome sequence of strain S55T also reveals the presence of enzymatic machinery required for organic matter decomposition. Soil metatranscriptomic analyses found 132 genes from strain S55T being expressed in the forest soil, especially during winter. Our results suggest an important contribution of T. gabretensis S55T in the carbon cycle in the Picea abies coniferous forest. PMID:26546425

  3. Terracidiphilus gabretensis gen. nov., sp. nov., an Abundant and Active Forest Soil Acidobacterium Important in Organic Matter Transformation.

    PubMed

    García-Fraile, Paula; Benada, Oldrich; Cajthaml, Tomáš; Baldrian, Petr; Lladó, Salvador

    2016-01-01

    Understanding the activity of bacteria in coniferous forests is highly important, due to the role of these environments as a global carbon sink. In a study of the microbial biodiversity of montane coniferous forest soil in the Bohemian Forest National Park (Czech Republic), we succeeded in isolating bacterial strain S55(T), which belongs to one of the most abundant operational taxonomic units (OTUs) in active bacterial populations, according to the analysis of RNA-derived 16S rRNA amplicons. The 16S rRNA gene sequence analysis showed that the species most closely related to strain S55(T) include Bryocella elongata SN10(T) (95.4% identity), Acidicapsa ligni WH120(T) (95.2% identity), and Telmatobacter bradus TPB6017(T) (95.0% identity), revealing that strain S55(T) should be classified within the phylum Acidobacteria, subdivision 1. Strain S55(T) is a rod-like bacterium that grows at acidic pH (3 to 6). Its phylogenetic, genotypic, phenotypic, and chemotaxonomic characteristics indicate that strain S55(T) corresponds to a new genus within the phylum Acidobacteria; thus, we propose the name Terracidiphilus gabretensis gen. nov., sp. nov. (strain S55(T) = NBRC 111238(T) = CECT 8791(T)). This strain produces extracellular enzymes implicated in the degradation of plant-derived biopolymers. Moreover, analysis of the genome sequence of strain S55(T) also reveals the presence of enzymatic machinery required for organic matter decomposition. Soil metatranscriptomic analyses found 132 genes from strain S55(T) being expressed in the forest soil, especially during winter. Our results suggest an important contribution of T. gabretensis S55(T) in the carbon cycle in the Picea abies coniferous forest. PMID:26546425

  4. Minerals yearbook, 1993: Nonrenewable organic materials. Annual report

    SciTech Connect

    Cantrell, R.L.

    1995-02-01

    The U.S. nonrenewable organics industry ranks third in terms of value in the United States behind the automotive and petroleum industries, in respective order of importance. In 1993, the organics industry--including feedstocks and salable nonfuel petroleum byproducts--was valued at more than $90 billion, f.o.b. plant, according to the U.S. International Trade Commission (ITC). Basic raw material feedstock costs calculated from U.S. Department of Energy (DOE) information were about $12.5 billion, based on point-of-origin prices for crude petroleum, dry natural gas, and liquid fractions, plus coal and salable downstream residual byproducts.

  5. Parameters for the Pyrolysis of Organic Material - Perchlorate Mixtures

    NASA Astrophysics Data System (ADS)

    Steininger, Harald; Goesmann, Fred; Goetz, Walter

    2013-04-01

    The ESA-lead Mars rover ExoMars (launch in 2018) will carry a suit of instruments, one of the in-struments is the Mars Organic Molecule Analyzer MOMA. Organic material in the Martian soil will be either pyrolyzed at temperatures of up to 1000°C and separated by gas chromatography or volatilized with the help of an UV-laser. A mass spectrometer will be the detector for both methods. Chlorinated organics have been detected in pyroly-sis GC-MS experiments on Mars two times. The first time during the Viking mission in 1976 and a second time with the Sample Analysis on Mars (SAM) in-strument onboard the Curiosity rover in 2012. [1] [2] The presence of perchlorates found by the Phoenix mission in 2008 [3] lead to the discovery that organic molecules not only get oxidized during pyrolysis, but also chlorinated organic compounds can be pro-duced. [4] The parameters used for pyrolysis and the sample composition especially the distribution of organics and perchlorates within the sample and the concentrations of organics and perchlorate have a huge influence on the products created. It is possible to change the condi-tions of the pyrolysis by spatially separating the organ-ics from the perchlorates that the chloromethanes get the major product of the pyrolysis. This might help to understand the results of the (SAM) instrument yield-ing mono-, di- and trichloromethane and a chlorinated 4-hydrocarbon molecule. References: [1] Biemann K et al. (1977) JGR, 82, 4641-4658. [2] Grotzinger J. P et al. (2011) AGU Fall Meeting U13A-01 [3] Hecht M. H., et al. (2009) Science, 325 64-67. [4] Steininger H., Goesmann F., Goetz W. (2011) Planet. & Space Sci., 71, 9-17. Acknowledgments: This work was funded by DLR (FKZ 50QX1001)

  6. Organic Materials for Time-Temperature Integrator Devices.

    PubMed

    Cavallini, Massimiliano; Melucci, Manuela

    2015-08-12

    Time-temperature integrators (TTIs) are devices capable of recording the thermal history of a system. They have an enormous impact in the food and pharmaceutical industries. TTIs exploit several irreversible thermally activated transitions such as recrystallization, dewetting, smoothening, chemical decomposition, and polymorphic transitions, usually considered drawbacks for many technological applications. The aim of this article is to sensitize research groups working in organic synthesis and surface science toward TTI devices, enlarging the prospects of many new materials. We reviewed the principal applications highlighting the need and criticisms of TTIs, which offer a new opportunity for the development of many materials. PMID:26156082

  7. Thermal and Electronic Transport in Inorganic and Organic Thermoelectric Materials

    NASA Astrophysics Data System (ADS)

    Tian, Zhiting

    In this talk, we will first talk about first-principles calculations of phonon and electron transport in inorganic thermoelectric materials. We will start with rocksalt PbTe and PbSe, and move on to wurtzite ZnO. We will emphasize the strategies to reduce the lattice thermal conductivity. Then we apply first-principles calculations to organic thermoelectric materials. The thermoelectric properties of doped polypyrrole (PPy) will be discussed. In addition, we will cover the chain confinement effects observed in amorphous polymer thin films using molecular dynamics simulations, which highlights the fundamental difference in heat conduction between crystalline polymers and amorphous polymers

  8. New materials for organic light-emitting diodes

    SciTech Connect

    Jacobs, S.J.; Pollagi, T.P.; Sinclair, M.B.; Scurlock, R.D.; Ogilby, P.R.

    1995-12-01

    We have investigated the performance of a class of heterocycles, 5, 10-dihetera-5,10-dihydroindeno[3,2b]indenes, as hole transport agents in simple double heterostructure organic light-emitting diodes with tris(8-hydroxyquinoline)aluminum (Alq). The best of these materials, 5,10-dihydroindolo[3,2b]indole, yields devices with luminance and lifetimes comparable to those obtained using N,N{prime}-di-(3-methylphenyl)-N,N{prime}diphenyl-4,4{prime}-diaminobiphenyl (TPD) as a hole transporting material.

  9. Measurement of organic/polymer material by phase modulation ellipsometry

    NASA Astrophysics Data System (ADS)

    Ji, Yong; Teboul, Eric; Kramer, Alan R.

    2004-06-01

    Due to they can be tailored to provide a wide range of physical properties and their easiness of processing and fabrication, polymeric materials have found widespread use in the manufacture of microwave, electronics, photonics and bio-tech systems. This paper presents the basic principle of phase modulation spectroscopic ellipsometer (PMSE) and its advantages over other ellipsometry in measuring polymer film. Used for thin film measurements ultra-thin dielectric, meal film and organic film, the PMSE technique is now used over a wide spectral range from the vacuum ultraviolet to the mid infrared. Film thickness ranging from Angstrom up to 50um can be measured by PMSE. Applications of PMSE on measurement and characterization of polymer/organic material are given in the paper.

  10. Organic Light-Emitting Transistors: Materials, Device Configurations, and Operations.

    PubMed

    Zhang, Congcong; Chen, Penglei; Hu, Wenping

    2016-03-01

    Organic light-emitting transistors (OLETs) represent an emerging class of organic optoelectronic devices, wherein the electrical switching capability of organic field-effect transistors (OFETs) and the light-generation capability of organic light-emitting diodes (OLEDs) are inherently incorporated in a single device. In contrast to conventional OFETs and OLEDs, the planar device geometry and the versatile multifunctional nature of OLETs not only endow them with numerous technological opportunities in the frontier fields of highly integrated organic electronics, but also render them ideal scientific scaffolds to address the fundamental physical events of organic semiconductors and devices. This review article summarizes the recent advancements on OLETs in light of materials, device configurations, operation conditions, etc. Diverse state-of-the-art protocols, including bulk heterojunction, layered heterojunction and laterally arranged heterojunction structures, as well as asymmetric source-drain electrodes, and innovative dielectric layers, which have been developed for the construction of qualified OLETs and for shedding new and deep light on the working principles of OLETs, are highlighted by addressing representative paradigms. This review intends to provide readers with a deeper understanding of the design of future OLETs. PMID:26833896

  11. Particle Rebound and Phase State of Secondary Organic Material

    NASA Astrophysics Data System (ADS)

    Bateman, A.; Bertram, A. K.; Martin, S. T.

    2014-12-01

    Secondary organic material (SOM) is produced in the atmosphere from the oxidation of volatile organic compounds emitted from anthropogenic and biogenic sources. Aerosol particles, composed in part of SOM, play important roles in climate and air quality by scattering/absorbing radiation and serving as cloud condensation nuclei (CCN). The magnitude of climate-relevant perturbations depends on particle chemical composition, hygroscopic growth, and phase state, among other factors. Herein, the hygroscopic influence on particle rebound and the phase state of particles composed of isoprene, toluene, and α-pinene secondary organic material (SOM) was studied. Particle rebound measurements were obtained from 5 to 95% RH using a three-arm impaction apparatus. The experimentally determined rebound fractions were compared with results from a model of the rebound process that took into account the particle kinetic energy, van der Waals forces, and RH-dependent capillary forces. Comparison of the experimental and modeled indicated particles softened due to water uptake. For low RH values, the model explained the rebound behavior for all studied SOMs. At higher RH values specific to each SOM, however, particle rebound was no longer observed, and the model did not capture this behavior. Calibration experiments using sucrose particles of variable known viscosities showed the transition from non-rebounding to rebounding particles occurred for viscosity values from 100 to 1 Pa s, corresponding to a transition from semisolid to liquid material. The implication of the differing RH-dependent behaviors among the SOMs is that each SOM has a specific and quantitatively different interaction with water. A linear correlation between rebound fraction and hygroscopic growth factor was demonstrated, implying that absorbed water volume is the governing factor of viscosity for the studied classes of SOM. The findings of this study suggest that both the chemical composition and the ambient

  12. Evaporation Rate and Saturated Vapor Pressure of Functional Organic Materials

    NASA Astrophysics Data System (ADS)

    Yase, Kiyoshi; Takahashi, Yoshikazu; Ara-kato, Norihiko; Kawazu, Akira

    1995-02-01

    The evaporation rate and saturated vapor pressure (p) for functional organic materials have been evaluated by thermogravimetry in vacuum. A series of metal phthalocyanines (M-Pc) such as Cu-Pc, Ni-Pc, Pb-Pc and TiO-Pc, Tris(8-hydroxy-quinoline) aluminum complex ( Alq3), fullerene (C60) and tetrathiafulvalene (TTF), tetracyanoquinodimethane (TCNQ) and TTF-TCNQ are examined, together with the relationship between p and the enthalpy of evaporation.

  13. Novel organic-inorganic hybrid and nano-structured materials

    NASA Astrophysics Data System (ADS)

    Jin, Danliang

    Organic polymers, i.e. polymethacrylates and polystyrene, and inorganic silica were successfully integrated covalently into one body, i.e. hybrid materials, at molecular level in a continuum ranging from pure polymer to pure silica via the sol-gel process. The synthetic conditions have been systematically studied and optimized. A fast and convenient method for the synthesis of polymethacrylate-silica hybrids with significantly low volume-shrinkages has been developed to address the intrinsic problems of the sol-gel process, i.e. large volume shrinkage and long drying times. The relationship of properties of the hybrids with the structures and organic-inorganic compositions have been established. The density, hardness and thermal stability increase with the silica content. Atomic force microscopy study of the morphology shows that the transparent hybrid materials, in which the polymer chains have a strong and intimate interaction with the silica matrix, have significantly different surface features from a translucent control sample. The compressive behavior of the hybrid materials is completely different from that of traditional composites. Toughness of the hybrid materials can be maximized and the strength can be dramatically increased by varying the silica content. Possible mechanisms for the formation of hybrid materials are proposed. Potential applications of the hybrid materials as dental fillers and cation exchangers were investigated. Amorphous silica was functionalized by doping with optically active compounds such as scD-glucose, diphenyl tartaric acid and maltose. The resultant nano-structured materials show excellent optical transparency to visible light. Optical rotation of the materials in the solid state was demonstrated quantitatively to be the same as that in solution. The specific rotation can be calculated directly according to Biot's equation. A non-surfactant templating approach has been developed for the preparation of mesoporous silica by

  14. Resistance to forced airflow through layers of composting organic material.

    PubMed

    Teixeira, Denis Leocádio; de Matos, Antonio Teixeira; Melo, Evandro de Castro

    2015-02-01

    The objective of this study was to adjust equations to estimate the static pressure gradient of airflow through layers of organic residues submitted to two stages of biochemical degradation, and to evaluate the static pressure drop of airflow thought the material layer. Measurements of static pressure drop in the layers of sugarcane bagasse and coffee husks mixed with poultry litter on day 0 and after 30 days of composting were performed using a prototype with specific airflow rates ranging from 0.02 to 0.13 m(3) s(-1) m(-2). Static pressure gradient and specific airflow rate data were properly fit to the Shedd, Hukill & Ives and Ergun models, which may be used to predict the static pressure gradient of air to be blown through the organic residue layers. However, the Shedd model was that which best represented the phenomenon studied. The static pressure drop of airflow increased as a power of the material layer thickness and showed tendency for decreasing with the biochemical degradation time of the organic material. PMID:25536861

  15. Solvent extraction of polychlorinated organic compounds from porous materials

    SciTech Connect

    Knowles, V.M.

    1988-07-19

    A method of reducing the level of hexachlorinated organic compounds selected from hexachloroethane, hexachlorobutadiene, hexachlorobenzene, or mixtures thereof to a non-hazardous level in a solid, porous DERAKANE vinyl ester resin, which has been previously used as the material of construction of a cell to produce chlorine, which vinyl ester resin was in contact with chlorine during chlorine manufacture is descried which comprises: (a) contacting the hexachlorinated compound-containing porous vinyl ester resin with an extraction solvent wherein the extraction solvent is selected from chloroform, carbon tetrachloride, trichlorethane, methyl chloroform, tetrachloroethane, perchloroethylene, benzene, toluene, xylene, acetone, methyl ethyl ketone, or mixtures thereof, at a temperature and for a time sufficient to remove the absorbed hexachlorinated organic compound; and (b) separating the hexachlorianated organic compound-containing extraction solvent and vinyl ester resin.

  16. Metal-Organic Frameworks as Sensory Materials and Imaging Agents

    PubMed Central

    Liu, Demin; Lu, Kuangda; Poon, Christopher

    2014-01-01

    Metal-organic frameworks (MOFs) are a class of hybrid materials self-assembled from organic bridging ligands and metal ion/cluster connecting points. The combination of a variety of organic linkers, metal ions/clusters, and structural motifs can lead to an infinite array of new materials with interesting properties for many applications. In this Forum article, we discuss the design and applications of MOFs in chemical sensing and biological imaging. The first half of this article focuses on the development of MOFs as chemical sensors by highlighting how unique attributes of MOFs can be utilized to enhance sensitivity and selectivity. We also discuss some of the issues that need to be addressed in order to develop practically useful MOF sensors. The second half of this article focuses on the design and applications of nanoscale metal-organic frameworks (NMOFs) as imaging contrast agents. NMOFs possess several interesting attributes, such as high cargo loading capacity, ease of post-modification, tunable size and shape, and intrinsic biodegradability, to make them excellent candidates as imaging contrast agents. We discuss the use of representative NMOFs in magnetic resonance imaging (MRI), X-ray computed tomography (CT), and optical imaging (OI). Although still in their infancy, we believe that the compositional tunability and mild synthetic conditions of NMOF imaging agents should greatly facilitate their further development for clinical translation. PMID:24251853

  17. Semivolatile particulate organic material in southern Africa during SAFARI 2000

    NASA Astrophysics Data System (ADS)

    Eatough, D. J.; Eatough, N. L.; Pang, Y.; Sizemore, S.; Kirchstetter, T. W.; Novakov, T.; Hobbs, P. V.

    2003-07-01

    During August and September 2000, the University of Washington's (UW) Cloud and Aerosol Research Group (CARG) with its Convair-580 research aircraft participated in the Southern African Fire-Atmosphere Research Initiative (SAFARI) 2000 field study in southern Africa. Aboard this aircraft was a Particle Concentrator-Brigham Young University Organic Sampling System (PC-BOSS), which was used to determine semivolatile particulate material with a diffusion denuder sampler. Denuded quartz filters and sorbent beds in series were used to measure nonvolatile and semivolatile materials, respectively. Results obtained with the PC-BOSS are compared to those obtained with conventional quartz-quartz and Teflon-quartz filter pack samplers. Various 10-120 min integrated samples were collected during flights through the free troposphere, in the atmospheric boundary layer, and in plumes from savanna fires. Significant fine particulate semivolatile organic compounds (SVOC) were found in all samples. The SVOC was not collected by conventional filter pack samplers and therefore would not have been determined in previous studies that used only filter pack samplers. The SVOC averaged 24% of the fine particulate mass in emissions from the fires and 36% of the fine particulate mass in boundary layer samples heavily impacted by aged emissions from savanna fires. Concentrations of fine particulate material in the atmospheric mixed layer heavily impacted by aged savanna fire emissions averaged 130 μg m-3. This aerosol was 85% carbonaceous material.

  18. Molecular Design of Benzodithiophene-Based Organic Photovoltaic Materials.

    PubMed

    Yao, Huifeng; Ye, Long; Zhang, Hao; Li, Sunsun; Zhang, Shaoqing; Hou, Jianhui

    2016-06-22

    Advances in the design and application of highly efficient conjugated polymers and small molecules over the past years have enabled the rapid progress in the development of organic photovoltaic (OPV) technology as a promising alternative to conventional solar cells. Among the numerous OPV materials, benzodithiophene (BDT)-based polymers and small molecules have come to the fore in achieving outstanding power conversion efficiency (PCE) and breaking 10% efficiency barrier in the single junction OPV devices. Remarkably, the OPV device featured by BDT-based polymer has recently demonstrated an impressive PCE of 11.21%, indicating the great potential of this class of materials in commercial photovoltaic applications. In this review, we offered an overview of the organic photovoltaic materials based on BDT from the aspects of backbones, functional groups, alkyl chains, and device performance, trying to provide a guideline about the structure-performance relationship. We believe more exciting BDT-based photovoltaic materials and devices will be developed in the near future. PMID:27251307

  19. Monothioanthraquinone as an organic active material for greener lithium batteries

    NASA Astrophysics Data System (ADS)

    Iordache, Adriana; Maurel, Vincent; Mouesca, Jean-Marie; Pécaut, Jacques; Dubois, Lionel; Gutel, Thibaut

    2014-12-01

    In order to reduce the environmental impact of human activities especially transportation and portable electronics, a more sustainable way is required to produce and store electrical energy. Actually lithium battery is one of the most promising solutions for energy storage. Unfortunately this technology is based on the use of transition metal-based active materials for electrodes which are rare, expensive, extracted by mining, can be toxic and hard to recycle. Organic materials are an interesting alternative to replace inorganic counterparts due to their high electrochemical performances and the possibility to produce them from renewable resources. A quinone derivative is synthetized and investigated as novel active material for rechargeable lithium ion batteries which shows higher performances.

  20. Microgravity Processing and Photonic Applications of Organic and Polymeric Materials

    NASA Technical Reports Server (NTRS)

    Frazier, Donald O.; Paley, Mark S.; Penn, Benjamin G.; Abdeldayem, Hossin A.; Smith, David D.; Witherow, William K.

    1997-01-01

    Some of the primary purposes of this work are to study important technologies, particularly involving thin films, relevant to organic and polymeric materials for improving applicability to optical circuitry and devices and to assess the contribution of convection on film quality in unit and microgravity environments. Among the most important materials processing techniques of interest in this work are solution-based and by physical vapor transport, both having proven gravitational and acceleration dependence. In particular, PolyDiAcetylenes (PDA's) and PhthaloCyanines (Pc's) are excellent NonLinear Optical (NLO) materials with the promise of significantly improved NLO properties through order and film quality enhancements possible through microgravity processing. Our approach is to focus research on integrated optical circuits and optoelectronic devices relevant to solution-based and vapor processes of interest in the Space Sciences Laboratory at the Marshall Space Flight Center (MSFC). Modification of organic materials is an important aspect of achieving more highly ordered structures in conjunction with microgravity processing. Parallel activities include characterization of materials for particular NLO properties and determination of appropriation device designs consistent with selected applications. One result of this work is the determination, theoretically, that buoyancy-driven convection occurs at low pressures in an ideal gas in a thermalgradient from source to sink. Subsequent experiment supports the theory. We have also determined theoretically that buoyancy-driven convection occurs during photodeposition of PDA, an MSFC-patented process for fabricating complex circuits, which is also supported by experiment. Finally, the discovery of intrinsic optical bistability in metal-free Pc films enables the possibility of the development of logic gate technology on the basis of these materials.

  1. On Organic Material in E Ring Ice Grains

    NASA Astrophysics Data System (ADS)

    Postberg, F.; Khawaja, N.; Reviol, R.; Nölle, L.; Klenner, F.; Hsu, H. W.; Horanyi, M.

    2015-12-01

    Pure water ice dominates the composition of the micron and sub-micron sized dust particles in Saturn's E-ring, a ring constantly replenished by active ice jets of the moon Enceladus [1]. Details about the composition of this tenuous, optically thin ring can only be constrained by in situ measurements. The Cosmic Dust Analyzer (CDA) onboard Cassini investigates the composition of these grains by cationic time-of-flight mass spectra of individual ice grains hitting the instruments target surface. From these spectra three compositional types of E ring ice grains have been identified previously [2,3]: Type-1: Almost pure water, Type-2: Enriched in organics, and Type-3: Enriched in salt. Unlike Type-1 and 3, organic-enriched Type-2 spectra have not yet been investigated in depth. Here we report the first detailed compositional analysis of this type. The spectra analysis is supported by a large-scale laboratory ground campaign yielding a library of analogue spectra for organic material embedded in a water ice matrix. In contrast to Type 1 and 3, Type-2 spectra display a great compositional diversity, which indicates varying contributions of several organic species. So far we have identified characteristic fragment patterns of at least three classes of organic compounds: aromatic species, amines, and carbonyl group species. Work is in progress to quantify concentrations of the identified species and to assign yet un-specified organic mass lines in Type 2 spectra. Due to the dynamical evolution of the orbital elements of E ring grains a large fraction collides with the icy moons embedded in the E ring. Therefore, the organic components identified by CDA can accumulate on the surfaces of these bodies over time. Ref: :[1]Kempf et al., Icarus-206, 2010. [2]Postberg et al., Nature-459, 2009. [3]Postberg et al., Icarus-193, 2008.

  2. Compositional effects of organic material in HC potential assessment

    NASA Astrophysics Data System (ADS)

    Luo, W. P.; Tsai, L. Y.

    2015-12-01

    Studies of petroleum system is the main theme of hydrocarbon potential assessment, in which the characteristics of source rock is especially worth noticed. In recent years, besides the growth of conventional hydrocarbon resources being rapidly utilized, the exploration of unconventional deposits is getting more and more important. Since Taiwan has a strong energy demand and still highly relied on imported fossil fuel, the development of unconventional gas resources needs to be considered. This research discussed the relationship among characteristics and thermal maturity of different organic material versus their hydrocarbon potential. In order to compare the compositional effects from different organic material, torbanites from Huangxian basin, China and Miocene humic coal from Chuhuangkeng Anticline (one of the most productive oil and gas fields), Taiwan were examined and compared. Torbanites from China had relatively low maturation with vitrinite reflectance 0.38~0.51%, whereas the maturation of humic coal from Chuhuangkeng Anticline are a little bit higher with vitrinite reflectance 0.55~0.6%, plus some methane explored. Methods of study include petrographic analysis, vitrinite reflectance measurement (Ro%), Rock-Eval pyrolysis, and other geochemical parameters. The conclusions were derived after comparing experimental results and the regional geologic information of samples studied. In conclude, sample from China is type I kerogen, and its organic matter is mostly algae, whereas the humic coal sample from Taiwan belongs to type III kerogen. The analytic results indicate that the characteristics organic matters affect their maturity. Even though the thermal history and depositional environments are different in Taiwan and China, their organic micelles still exhibit a similar trend in the process of coalification. The role of maceral composition played in HC potential needs to be considered in future shale gas exploration.

  3. Ultra high barrier materials for encapsulation of flexible organic electronics

    NASA Astrophysics Data System (ADS)

    Logothetidis, S.; Laskarakis, A.; Georgiou, D.; Amberg-Schwab, S.; Weber, U.; Noller, K.; Schmidt, M.; Küçükpinar-Niarchos, E.; Lohwasser, W.

    2010-09-01

    The encapsulation of the active layers (organic semiconductors, electrodes, transparent conductive oxides, etc.) of organic electronic devices developed onto flexible polymeric substrates is one of the most challenging issues in the rapidly emerging area of organic electronics. The importance for the protection of the active layers arises from the fact that these are very sensitive when they are subjected to the atmosphere, since the permeation of the atmosphere's water vapour (H2O) and oxygen (O2) gases induces corrosion effects, film delamination and finally, failure of the organic electronic device. In addition, the encapsulation layers contribute to the long-term stability of the whole device enabling its use in outdoor environments (e.g. in the case of flexible photovoltaic cells-OPVs). A promising approach for the encapsulation of flexible organic electronics includes the development of multilayers that consist of hybrid polymer materials and inorganic layers onto flexible polymeric substrates, such as poly(ethylene terephthalate) (PET). This approach leads to a significant improvement of the barrier performance of the whole structure, due to the synergetic effect of the confinement of the permeation to the defect zones of the inorganic layer, and the formation of chemical bonds between the hybrid polymer and the inorganic layer. The knowledge of their optical properties and their correlation with their barrier performance are of major importance since it will contribute towards the optimization of their functionality. In this work, we provide an overview on the results concerning the use of hybrid polymers as ultra high barrier materials and moreover we discuss on the effect of inclusion of SiO2 nano-particles on their optical properties and barrier performance.

  4. Nonlinear optical properties and nonlinear optical probes of organic materials

    NASA Astrophysics Data System (ADS)

    Meredith, Gerald R.

    1992-02-01

    Nonlinear optical processes and electro-optical effects are expected to have increasing importance as the information age matures and photonics augment electronics in various high density and high bandwidth technologies. Whereas for electronics the emphasis is in construction of smaller device structures from a few parent materials, for organic materials the direction of materials research has been reversed. For some time it's been known that some molecular structures engender exceptionally large molecular nonlinear-polarization responses. If such molecules could be assembled in convenient, versatile, and reliable ways, the resulting materials would be very useful or even enabling in various photonics applications. The mature science and art of chemistry allows very good control over molecular composition and structure and, as will be illustrated in this talk, our knowledge of hyperpolarizability structure- property relationships is advancing rapidly. However, the science of fabrication and arrangement in molecular ensembles and polymers is rather primitive. Thus the goal to develop the appropriately structured materials for utilization in nonlinear and electro-optics has fostered the widespread use of nonlinear optical processes to probe the nature of supramolecular order and assembly. Examples of intrinsic and artificially assembled structures of crystals, molecular aggregates, polymeric orientational electrets and molecular mono- and multi-layer thin films will be shown. Nonlinear optical processes, primarily second-harmonic generation, provide unique probes of these structures, their assembly, and evolution.

  5. Application of scatterometry to measure organic material profile

    NASA Astrophysics Data System (ADS)

    Koo, Sunyoung; Ban, Keundo; Lim, Chang-moon; Bok, Cheolkyu; Moon, Seung-Chan; Kim, Jinwoong

    2006-03-01

    Scanning Electron Microscope (SEM) has been typical methods for measuring CD of nanopatterns until ArF process was introduced. However in case of ArF process, this method has serious drawback such as shrinkage of organic material by the irradiation of high-energy electron beam. The optical scatterometry system is considered to be promising method for measuring CD due to no damage on organic materials. Sub-80nm node gate was selected because of its measurement stability. CD, profile and thickness are compared with those measured by CD-SEM, cress-section SEM. The correlation degree is shown as GOF, R2, and Profile. Based on merit of speed, easiness and accurate measurement, optical CD method has been applied to CD uniformity. CD uniformity measured by OCD was very similar to that measured by SEM on gate pattern. Based on this result, OCD was applied for the improvement of CD uniformity combined with ASML's does-mapper in technology. We investigated the variation of thickness of organic BARC over topology of various size line and space patterned poly-Si by OCD.

  6. Secondary organic material formed by methylglyoxal in aqueous aerosol mimics

    NASA Astrophysics Data System (ADS)

    Sareen, N.; Schwier, A. N.; Shapiro, E. L.; Mitroo, D.; McNeill, V. F.

    2010-02-01

    We show that methylglyoxal forms light-absorbing secondary organic material in aqueous ammonium sulfate and ammonium nitrate solutions mimicking tropospheric aerosol particles. The kinetics were characterized using UV-Vis spectrophotometry. The results suggest that the bimolecular reaction of methylglyoxal with an ammonium or hydronium ion is the rate-limiting step for the formation of light-absorbing species, with kNH4+II=5×10-6 M-1 min-1 and kH3O+II≤10-3 M-1 min-1. Evidence of aldol condensation products and oligomeric species up to 759 amu was found using chemical ionization mass spectrometry with a volatilization flow tube inlet (Aerosol-CIMS). Tentative identifications of carbon-nitrogen species and a sulfur-containing compound were also made using Aerosol-CIMS. Aqueous solutions of methylglyoxal, with and without inorganic salts, exhibit significant surface tension depression. These observations add to the growing body of evidence that dicarbonyl compounds may form secondary organic material in the aerosol aqueous phase, and that secondary organic aerosol formation via heterogeneous processes may affect seed aerosol properties.

  7. Two wheat (Triticum aestivum) pathogenesis-related 10 (PR-10) transcripts with distinct patterns of abundance in different organs.

    PubMed

    Mohammadi, Mohsen; Srivastava, Sanjeeva; Hall, Jocelyn C; Kav, Nat N V; Deyholos, Michael K

    2012-06-01

    PR-10 genes encode small, acidic, intracellular proteins that respond to abiotic and biotic stimuli. Transgenic expression of PR-10 genes has been shown to enhance early seedling growth of dicots in saline environments. To identify candidate PR-10 genes in cereals for increasing stress tolerance, we conducted phylogenetic analyses and real-time polymerase chain reaction of representatives of the two major clades of putative PR-10 genes in wheat. We observed that the abundance of BQ752893 was generally greater than the abundance of CV778999, particularly when measured in roots across four wheat genotypes. However, CV778999 transcripts were more abundant than BQ752893 in flag leaves. These data suggest that the transcripts define two functionally divergent groups of PR-10 type genes in wheat, both of which may be suitable targets for biotechnological manipulation under different circumstances. PMID:21818707

  8. Renewable synthetic diesel fuel from triglycerides and organic waste materials

    SciTech Connect

    Hillard, J.C.; Strassburger, R.S.

    1986-03-01

    A renewable, synthetic diesel fuel has been developed that employs ethanol and organic waste materials. These organic materials, such as soybean oil or animal fats, are hydrolized to yield a mixture of solid soap like materials and glycerol. These soaps, now soluble in ethanol, are blended with ethanol; the glycerol is nitrated and added as well as castor oil when necessary. The synthetic fuel is tailored to match petroleum diesel fuel in viscosity, lubricity and cetane quality and, therefore, does not require any engine modifications. Testing in a laboratory engine and in a production Oldsmobile Cutlass has revealed that this synthetic fuel is superior to petroleum diesel fuel in vehicle efficiency, cetane quality, combustion noise, cold start characteristics, exhaust odor and emissions. Performance characteristics are indistinguishable from those of petroleum diesel fuel. These soaps are added to improve the calorific value, lubricity and cetane quality of the ethanol. The glycerol from the hydrolysis process is nitrated and added to the ethanol as an additional cetane quality improver. Caster oil is added to the fuel when necessary to match the viscosity and lubricity of petroleum diesel fuel as well as to act as a corrosion inhibitor, thereby, precluding any engine modifications. The cetane quality of the synthetic fuel is better than that of petroleum diesel as the fuel carries its own oxygen. The synthetic fuel is also completely miscible with petroleum diesel.

  9. Semivolatile Particulate Organic Material Southern Africa during SAFARI 2000

    NASA Technical Reports Server (NTRS)

    Eatough, D. J.; Eatough, N. L.; Pang, Y.; Sizemore, S.; Kirchstetter, T. W.; Novakov, T.

    2005-01-01

    During August and September 2000, the University of Washington's Cloud and Aerosol Research Group (CARG) with its Convair-580 research aircraft participated in the Southern African Fire-Atmosphere Research Initiative (SAFARI) 2000 field study in southern Africa. Aboard this aircraft was a Particle Concentrator-Brigham Young University Organic Sampling System (PC-BOSS), which was used to determine semivolatile particulate material with a diffusion denuder sampler. Denuded quartz filters and sorbent beds in series were used to measure nonvolatile and semivolatile materials, respectively. Results obtained with the PC-BOSS are compared to those obtained with conventional quartz-quartz and Teflon-quartz filter pack samplers. Various 10-120 min integrated samples were collected during flights through the h e troposphere, in the atmospheric boundary layer, and in plumes from savanna fires. Significant fine particulate semivolatile organic compounds (SVOC) were found in all samples. The SVOC was not collected by conventional filter pack samplers and therefore would not have been determined in previous studies that used only filter pack samplers. The SVOC averaged 24% of the fine particulate mass in emissions from the fires and 36% of the fine particulate mass in boundary layer samples heavily impacted by aged emissions from savanna fires. Concentrations of fine particulate material in the atmospheric mixed layer heavily impacted by aged savanna frre emissions averaged 130 micrograms per cubic meter. This aerosol was 85% carbonaceous mated.

  10. Virtual screening of electron acceptor materials for organic photovoltaic applications

    NASA Astrophysics Data System (ADS)

    Halls, Mathew D.; Djurovich, Peter J.; Giesen, David J.; Goldberg, Alexander; Sommer, Jonathan; McAnally, Eric; Thompson, Mark E.

    2013-10-01

    Virtual screening involves the generation of structure libraries, automated analysis to predict properties related to application performance and subsequent screening to identify lead systems and estimate critical structure-property limits across a targeted chemical design space. This approach holds great promise for informing experimental discovery and development efforts for next-generation materials, such as organic semiconductors. In this work, the virtual screening approach is illustrated for nitrogen-substituted pentacene molecules to identify systems for development as electron acceptor materials for use in organic photovoltaic (OPV) devices. A structure library of tetra-azapentacenes (TAPs) was generated by substituting four nitrogens for CH at 12 sites on the pentacene molecular framework. Molecular properties (e.g. ELUMO, Eg and μ) were computed for each candidate structure using hybrid DFT at the B3LYP/6-311G** level of theory. The resulting TAPs library was then analyzed with respect to intrinsic properties associated with OPV acceptor performance. Marcus reorganization energies for charge transport for the most favorable TAP candidates were then calculated to further determine suitability as OPV electron acceptors. The synthesis, characterization and OPV device testing of TAP materials is underway, guided by these results.

  11. Spin-on organic hardmask materials in 70nm devices

    NASA Astrophysics Data System (ADS)

    Oh, Chang-Il; Uh, Dong-Seon; Kim, Do-Hyeon; Lee, Jin-Kuk; Yun, Hui-Chan; Nam, Irina; Kim, Min-Soo; Yoon, Kyong-Ho; Hyung, Kyung-Hee; Tokareva, Nataliya; Cheon, Hwan-Sung; Kim, Jong-Seob; Chang, Tu-Won

    2007-03-01

    In ArF lithography for < 90nm L/S, amorphous carbon layer (ACL) deposition becomes inevitable process because thin ArF resist itself can not provide suitable etch selectivity to sub-layers. One of the problems of ACL hardmask is surface particles which are more problematic in mass production. Limited capacity, high cost-of-ownership, and low process efficiency also make ACL hardmask a dilemma which can not be ignored by device makers. One of the answers to these problems is using a spin-on organic hardmask material instead of ACL hardmask. Therefore, several processes including bi-layer resist process (BLR), tri-layer resist process (TLR), and multi-layer resist process (MLR) have been investigated. In this paper, we have described spin-on organic hardmask materials applicable to 70nm memory devices. Applications to tri-layer resist process (TLR) were investigated in terms of photo property, etch property and process compatibility. Based on the test results described in this paper, our spin-on hardmask materials are expected to be used in mass production.

  12. Radiation effects on organic materials in nuclear plants. Final report

    SciTech Connect

    Bruce, M B; Davis, M V

    1981-11-01

    A literature search was conducted to identify information useful in determining the lowest level at which radiation causes damage to nuclear plant equipment. Information was sought concerning synergistic effects of radiation and other environmental stresses. Organic polymers are often identified as the weak elements in equipment. Data on radiation effects are summarized for 50 generic name plastics and 16 elastomers. Coatings, lubricants, and adhesives are treated as separate groups. Inorganics and metallics are considered briefly. With a few noted exceptions, these are more radiation resistant than organic materials. Some semiconductor devices and electronic assemblies are extremely sensitive to radiation. Any damage threshold including these would be too low to be of practical value. With that exception, equipment exposed to less than 10/sup 4/ rads should not be significantly affected. Equipment containing no Teflon should not be significantly affected by 10/sup 5/ rads. Data concerning synergistic effects and radiation sensitization are discussed. The authors suggest correlations between the two effects.

  13. Two-dimensional nanoarchitectonics: organic and hybrid materials.

    PubMed

    Govindaraju, T; Avinash, M B

    2012-10-21

    Programmed molecular assemblies with molecular-level precision have always intrigued mankind in the quest to master the art of molecular engineering. In this regard, our review seeks to highlight the state of the art in supramolecular engineering. Herein we describe two-dimensional (2D) nanoarchitectonics of organic and organic-inorganic based hybrid materials. Molecular systems ranging from simpler hydrogen bonding driven bis-acylurea and cyclic dipeptide derivatives to complex peptoids, arylenes, cucurbiturils, biphenyls, organosilicons and organometallics, which involve a delicate interplay of multiple noncovalent interactions are discussed. These specifically chosen examples illustrate the molecular design principles and synthetic protocols to realize 2D nanosheets. The description also emphasizes the wide variety of functional properties and technological implications of these 2D nanomaterials besides an outlook for future progress. PMID:22782293

  14. Amplified Spontaneous Emission Properties of Semiconducting Organic Materials

    PubMed Central

    Calzado, Eva M.; Boj, Pedro G.; Díaz-García, María A.

    2010-01-01

    This paper aims to review the recent advances achieved in the field of organic solid-state lasers with respect to the usage of semiconducting organic molecules and oligomers in the form of thin films as active laser media. We mainly focus on the work performed in the last few years by our research group. The amplified spontaneous emission (ASE) properties, by optical pump, of various types of molecules doped into polystyrene films in waveguide configuration, are described. The various systems investigated include N,N′-bis(3-methylphenyl)-N,N′-diphenylbenzidine (TPD), several perilenediimide derivatives (PDIs), as well as two oligo-phenylenevinylene derivatives. The ASE characteristics, i.e., threshold, emission wavelength, linewidth, and photostability are compared with that of other molecular materials investigated in the literature. PMID:20640167

  15. Adsorption of chromate/organic-acid mixtures in aquifer materials

    SciTech Connect

    Fish, W.; Palmer, C.D.

    1991-07-15

    The overall objective of this project is to develop a fuller understanding of the interactions of mixtures of anionic co-contaminants with oxide-mineral surfaces. Our specific focus is on the competitive interactions of chromate and oxalic acid on ferric oxyhydroxide and on natural aquifer materials. Chromate and oxalate are of practical interest as widespread contaminants at many DOE facilities. However, these anions also are excellent model adsorbates for elucidating fundamental aspects of ionic adsorption processes, particularly with respect to organic acids.

  16. Mobility of organic solvents in water-saturated soil materials

    USGS Publications Warehouse

    Roy, W.R.; Griffin, R.A.

    1985-01-01

    This investigation presents an analysis of the mobility of 37 organic solvents in saturated soil-water systems, focusing on adsorption phenomena at the solid-liquid interface This analysis was made, in part, by applying predictive expressions that estimate the potential magnitude of adsorption by soil materials Of the 37 solvents considered, 19 were classified as either "very highly mobile" or "highly mobile" and, thus, would have little tendency to be retained by soils to a significant extent, 12 were considered to have medium mobility and 6 low mobility None of these solvents were in the immobile class The limited information available indicates that these predictive expressions yield satisfactory first approximations of the magnitude of adsorption of these solvents by soil materials ?? 1985 Springer-Verlag New York Inc.

  17. Biochemically designed polymers as self-organized materials

    NASA Astrophysics Data System (ADS)

    Alva, Shridhara; Sarma, Rupmoni; Marx, Kenneth A.; Kumar, Jayant; Tripathy, Sukant K.; Akkara, Joseph A.; Kaplan, David L.

    1997-02-01

    Self assembled molecular systems are a focus of attention for material scientists as they provide an inherent molecular level organization responsible for enhanced material properties. We have developed polymeric molecular systems with interesting optical properties by biochemical engineering, which can be self assembled to thin films. Horseradish peroxidase catalyzed polymerizations of phenolic monomers: 9-hydroxyquinoline-5-sulfonic acid, acid red and decyl ester (d&l isomers) of tyrosine, have been achieved in the presence of hydrogen peroxide. The polymer of 8- hydroxyquinoline-5-sulfonic acid acts as a polymeric ligand that can be used for metal ion sensing. The polymer of acid red, with azo functional groups in the polymer backbone, shows interesting optical properties. Amphiphilic derivatives of tyrosine self assemble into tubules from micelles in aqueous solutions. These tubules have been enzymatically polymerized to polymeric tubules. The tubules are of 5 micrometers average diameter and > 200 micrometers length. The formation and properties of these tubules are discussed.

  18. Organic materials in planetary and protoplanetary systems: nature or nurture?

    NASA Astrophysics Data System (ADS)

    Dalle Ore, C. M.; Fulchignoni, M.; Cruikshank, D. P.; Barucci, M. A.; Brunetto, R.; Campins, H.; de Bergh, C.; Debes, J. H.; Dotto, E.; Emery, J. P.; Grundy, W. M.; Jones, A. P.; Mennella, V.; Orthous-Daunay, F. R.; Owen, T.; Pascucci, I.; Pendleton, Y. J.; Pinilla-Alonso, N.; Quirico, E.; Strazzulla, G.

    2011-09-01

    Aims: The objective of this work is to summarize the discussion of a workshop aimed at investigating the properties, origins, and evolution of the materials that are responsible for the red coloration of the small objects in the outer parts of the solar system. Because of limitations or inconsistencies in the observations and, until recently, the limited availability of laboratory data, there are still many questions on the subject. Our goal is to approach two of the main questions in a systematic way: - Is coloring an original signature of materials that are presolar in origin ("nature") or stems from post-formational chemical alteration, or weathering ("nurture")? - What is the chemical signature of the material that causes spectra to be sloped towards the red in the visible? We examine evidence available both from the laboratory and from observations sampling different parts of the solar system and circumstellar regions (disks). Methods: We present a compilation of brief summaries gathered during the workshop and describe the evidence towards a primordial vs. evolutionary origin for the material that reddens the small objects in the outer parts of our, as well as in other, planetary systems. We proceed by first summarizing laboratory results followed by observational data collected at various distances from the Sun. Results: While laboratory experiments show clear evidence of irradiation effects, particularly from ion bombardment, the first obstacle often resides in the ability to unequivocally identify the organic material in the observations. The lack of extended spectral data of good quality and resolution is at the base of this problem. Furthermore, that both mechanisms, weathering and presolar, act on the icy materials in a spectroscopically indistinguishable way makes our goal of defining the impact of each mechanism challenging. Conclusions: Through a review of some of the workshop presentations and discussions, encompassing laboratory experiments as well

  19. Molecular materials for organic photovoltaics: small is beautiful.

    PubMed

    Roncali, Jean; Leriche, Philippe; Blanchard, Philippe

    2014-06-18

    An overview of some recent developments of the chemistry of molecular donor materials for organic photovoltaics (OPV) is presented. Although molecular materials have been used for the fabrication of OPV cells from the very beginning of the field, the design of molecular donors specifically designed for OPV is a relatively recent research area. In the past few years, molecular donors have been used in both vacuum-deposited and solution-processed OPV cells and both fields have witnessed impressive progress with power conversion efficiencies crossing the symbolic limit of 10 %. However, this progress has been achieved at the price of an increasing complexity of the chemistry of active materials and of the technology of device fabrication. This evolution probably inherent to the progress of research is difficult to reconcile with the necessity for OPV to demonstrate a decisive economic advantage over existing silicon technology. In this short review various classes of molecular donors are discussed with the aim of defining possible basic molecular structures that can combine structural simplicity, low molecular weight, synthetic accessibility, scalability and that can represent possible starting points for the development of simple and cost-effective OPV materials. PMID:24687246

  20. Computational screening of organic materials towards improved photovoltaic properties

    NASA Astrophysics Data System (ADS)

    Dai, Shuo; Olivares-Amaya, Roberto; Amador-Bedolla, Carlos; Aspuru-Guzik, Alan; Borunda, Mario

    2015-03-01

    The world today faces an energy crisis that is an obstruction to the development of the human civilization. One of the most promising solutions is solar energy harvested by economical solar cells. Being the third generation of solar cell materials, organic photovoltaic (OPV) materials is now under active development from both theoretical and experimental points of view. In this study, we constructed a parameter to select the desired molecules based on their optical spectra performance. We applied it to investigate a large collection of potential OPV materials, which were from the CEPDB database set up by the Harvard Clean Energy Project. Time dependent density functional theory (TD-DFT) modeling was used to calculate the absorption spectra of the molecules. Then based on the parameter, we screened out the top performing molecules for their potential OPV usage and suggested experimental efforts toward their synthesis. In addition, from those molecules, we summarized the functional groups that provided molecules certain spectrum capability. It is hoped that useful information could be mined out to provide hints to molecular design of OPV materials.

  1. Charge transport and injection in amorphous organic electronic materials

    NASA Astrophysics Data System (ADS)

    Tse, Shing Chi

    This thesis presents how we use various measuring techniques to study the charge transport and injection in organic electronic materials. Understanding charge transport and injection properties in organic solids is of vital importance for improving performance characteristics of organic electronic devices, including organic-light-emitting diodes (OLEDs), photovoltaic cells (OPVs), and field effect transistors (OFETs). The charge transport properties of amorphous organic materials, commonly used in organic electronic devices, are investigated by the means of carrier mobility measurements. Transient electroluminescence (EL) technique was used to evaluate the electron mobility of an electron transporting material--- tris(8-hydroxyquinoline) aluminum (Alq3). The results are in excellent agreement with independent time-of-flight (TOF) measurements. Then, the effect of dopants on electron transport was also examined. TOF technique was also used to examine the effects of tertiary-butyl (t-Bu) substitutions on anthracene derivatives (ADN). All ADN compounds were found to be ambipolar. As the degree of t-Bu substitution increases, the carrier mobilities decrease progressively. The reduction of carrier mobilities with increasing t-butylation can be attributed to a decrease in the charge-transfer integral or the wavefunction overlap. In addition, from TOF measurements, two naphthylamine-based hole transporters, namely, N,N'-diphenyl-N,N'-bis(1-naphthyl)(1,1'-biphenyl)-4,4'diamine (NPB) and 4,4',4"-tris(n-(2-naphthyl)-n-phenyl-amino)-triphenylamine (2TNATA) were found to possess electron-transporting (ET) abilities. An organic light-emitting diode that employed NPB as the ET material was demonstrated. The electron conducting mechanism of NPB and 2TNATA in relation to the hopping model will be discussed. Furthermore, the ET property of NPB applied in OLEDs will also be examined. Besides transient EL and TOF techniques, we also use dark-injection space-charge-limited current

  2. The effects of the 2010 flood on the composition and abundance of the terrestrial organic matter in sediments along the inner-shelf off the Changjiang Estuary, China

    NASA Astrophysics Data System (ADS)

    Li, X.; Bianchi, T. S.; Allison, M. A.; Chapman, P.; Yang, G.

    2011-12-01

    Surface sediments were collected within the primary depositional pathway along the inner-shelf off the Changjiang Estuary in winter 2009 and fall 2010 - before and after the 2010 flood in the Changjiang River. Multiple proxies (stable isotopes, lignin-phenols, pigments, cutins) were analyzed to examine the influence of this flooding event on the composition and abundance of river-derived terrestrial organic matter in sediments off the Changjiang Estuary. Elemental and stable isotope analyses showed significantly higher molar C/N ratios and enriched δ13C signatures for 2010 samples, which likely reflected inputs of C4 vascular plant materials. Post-flood concentrations of lignin-phenols were significantly lower in concentration than pre-flood concentrations in 2009. Lignin-phenol acid/aldehyde (Ad/Al) ratios, the lignin degradation index, showed significantly more degraded lignin post-flood in 2010 than that in 2009, which suggests greater inputs of lignins that were likely associated more with degraded soils, due to enhanced erosion from the flood, than surface plant litter. This was also in good agreement with higher inputs of another lignin soil proxy, the 3,5-Bd (3,5-dihydroxybenzoic acid) /V. Lignin-phenol source plots showed no significant differences in pre-and post flood sources, with sources largely consisting of a mixture of woody and non-woody gymnosperm and angiosperm inputs. Short lived radionuclides such as 7Be, 234Th analysis showed no apparent short-term sediment accumulation. The lack of evidence for new sediments deposited to the inner shelf after the flood was likely influenced in part, by the effects of extensive upstream damming on the Changjiang, especially the more recently constructed Three Gorges Dam.

  3. Measurement of reflection coefficients of organic and non-organic media and materials in UV spectrum

    NASA Astrophysics Data System (ADS)

    Klimkin, A. V.; Belov, V. V.; Vorobieva, L. P.; Prokopev, V. E.; Kurjak, A. V.; Sokovikov, V. G.

    2015-12-01

    Measurements of the diffuse reflection coefficients of organic and inorganic materials and media in solid, granular and liquid forms were made in the UV field of 230-400 nm. A single channel spectrometer with an integrating sphere was used. Relation between diffuse reflection coefficients and the structure and composition of the samples is discussed. These data allow us to estimate the prospect of machine vision systems application for the UV range in such areas as biology, geology, remote control of materials and media.

  4. Comparison of low-cost and engineered materials for phosphorus removal from organic-rich surface water.

    PubMed

    Boyer, Treavor H; Persaud, Amar; Banerjee, Poulomi; Palomino, Pedro

    2011-10-15

    Excess phosphorus (P) in lakes and rivers remains a major water quality problem on a global scale. As a result, new materials and innovative approaches to P remediation are required. Natural materials and waste byproduct materials from industrial processes have the potential to be effective materials for P removal from surface water. Advantages of natural and waste byproduct materials include their low-cost, abundant supply, and minimal preparation, especially compared with engineered materials, such as ion exchange resins and polymeric adsorbents. As a result, natural and waste byproduct materials are commonly referred to as low-cost materials. Despite the potential advantages of low-cost materials, there are critical gaps in knowledge that are preventing their effective use. In particular, there are limited data on the performance of low-cost materials in surface waters that have high concentrations of natural organic matter (NOM), and there are no systematic studies that track the changes in water chemistry following treatment with low-cost materials or compare their performance with engineered materials. Accordingly, the goal of this work was to evaluate and compare the effectiveness of low-cost and engineered materials for P removal from NOM-rich surface water. Seven low-cost materials and three engineered materials were evaluated using jar tests and mini-column experiments. The test water was a surface water that had a total P concentration of 132-250 μg P/L and a total organic carbon concentration of 15-32 mg C/L. Alum sludge, a byproduct of drinking water treatment, and a hybrid anion exchange resin loaded with nanosize iron oxide were the best performing materials in terms of selective P removal in the presence of NOM and minimum undesirable secondary changes to the water chemistry. PMID:21767859

  5. Decontaminating materials used in ground water sampling devices: Organic contaminants

    SciTech Connect

    Parker, L.V.; Ranney, T.A.

    2000-12-31

    In these studies, the efficiency of various decontamination protocols was tested on small pieces of materials commonly used in ground water sampling devices. Three materials, which ranged in ability to sorb organic solutes, were tested: stainless steel (SS), rigid polyvinyl chloride (PVC), and polytetrafluoroethylene (PTFE). The test pieces were exposed to two aqueous test solutions: One contained three volatile organic compounds (VOCs) and one nitroaromatic compound, and the other contained four pesticides. Also, three types of polymetic tubing were exposed to pesticide solutions. Generally, the contact times were 10 minutes and 24 hours for sorption and desorption. The contaminants were removed from the nonpermeable SS and the less-sorptive rigid PVC test pieces simply by washing with a hot detergent solution and rinsing with hot water. Additional treatment was required for the PTFE test pieces exposed to the VOCs and for the low-density polyethylene (LDPE) tubing exposed to the pesticide test solution. Solvent rinsing did not improve removal of the three VOCs form the PTFE and only marginally improved removal of the residual pesticides from the LDPE. However, a hot water and detergent wash and rinse followed by oven drying at approximately 105 C was effective for removing the VOCs from the PTFE and substantially reduced pesticide contamination from the LDPE.

  6. Structural diversity in hybrid organic-inorganic lead iodide materials.

    PubMed

    Weber, Oliver J; Marshall, Kayleigh L; Dyson, Lewis M; Weller, Mark T

    2015-12-01

    The structural chemistry of hybrid organic-inorganic lead iodide materials has become of increasing significance for energy applications since the discovery and development of perovskite solar cells based on methylammonium lead iodide. Seven new hybrid lead iodide compounds have been synthesized and structurally characterized using single-crystal X-ray diffraction. The lead iodide units in materials templated with bipyridyl, 1,2-bis(4-pyridyl)ethane, 1,2-di(4-pyridyl)ethylene and imidazole adopt one-dimensional chain structures, while crystallization from solutions containing piperazinium cations generates a salt containing isolated [PbI6](4-) octahedral anions. Templating with 4-chlorobenzylammonium lead iodide adopts the well known two-dimensional layered perovskite structure with vertex shared sheets of composition [PbI4](2-) separated by double layers of organic cations. The relationships between the various structures determined, their compositions, stability and hydrogen bonding between the protonated amine and the iodide ions of the PbI6 octahedra are described. PMID:26634723

  7. Supramolecular organization of functional organic materials in the bulk and at organic/organic interfaces: a modeling and computer simulation approach.

    PubMed

    Muccioli, Luca; D'Avino, Gabriele; Berardi, Roberto; Orlandi, Silvia; Pizzirusso, Antonio; Ricci, Matteo; Roscioni, Otello Maria; Zannoni, Claudio

    2014-01-01

    The molecular organization of functional organic materials is one of the research areas where the combination of theoretical modeling and experimental determinations is most fruitful. Here we present a brief summary of the simulation approaches used to investigate the inner structure of organic materials with semiconducting behavior, paying special attention to applications in organic photovoltaics and clarifying the often obscure jargon hindering the access of newcomers to the literature of the field. Special attention is paid to the choice of the computational "engine" (Monte Carlo or Molecular Dynamics) used to generate equilibrium configurations of the molecular system under investigation and, more importantly, to the choice of the chemical details in describing the molecular interactions. Recent literature dealing with the simulation of organic semiconductors is critically reviewed in order of increasing complexity of the system studied, from low molecular weight molecules to semiflexible polymers, including the challenging problem of determining the morphology of heterojunctions between two different materials. PMID:24322782

  8. Testing of organic waste surrogate materials in support of the Hanford organic tank program. Final report

    SciTech Connect

    Turner, D.A.; Miron, Y.

    1994-01-01

    To address safety issues regarding effective waste management efforts of underground organic waste storage tanks at the Hanford Site, the Bureau of Mines conducted a series of tests, at the request of the Westinghouse Hanford company. In this battery of tests, the thermal and explosive characteristics of surrogate materials, chosen by Hanford, were determined. The surrogate materials were mixtures of inorganic and organic sodium salts, representing fuels and oxidants. The oxidants were sodium nitrate and sodium nitrite. The fuels were sodium salts of oxalate, citrate and ethylenediamine tetraacetic acid (EDTA). Polyethylene powder was also used as a fuel with the oxidant(s). Sodium aluminate was used as a diluent. In addition, a sample of FeCN, supplied by Hanford was also investigated.

  9. Organic/inorganic nanocomposite materials by electrospinning and their properties

    NASA Astrophysics Data System (ADS)

    Wang, Guan

    One-dimensional (1D) nanostructures, such as nanowires, nanobelts, nanofibers and nanotubes, have been the focus of intensive research due to their peculiar structures and resultant fascinating properties. However, the applications of 1D nanostructures have been hindered by the slow progress of the synthesis and characterization methods for these nanoscaled materials. Well controlled dimensionality, tailorable morphology and assembly, high phase purity and controllable crystallinity are major concerns when generating these nanostructures. In this work, a relatively simple technique---electrospinning---has been introduced for the preparation of 1D organic/inorganic nanocomposite materials. Materials under investigation include polymer/metal oxide (WO 3, MoO3) composite nanofibers and polymer/MWNT composite nanofibers. Notably, peculiar nanostructures, such as polycrystalline nanowires, nanoplatelets and nanobelts, can also be obtained after post-calcination processing on the nanocomposite materials. Spectroscopy techniques, such as XRD, SEM, TEM, AFM and Raman have been carried out to obtain structural and morphological information from the electrospun composite nanofibers. Meanwhile, some advanced characterization methods and measurements have been developed and designed to investigate the nanofibers from a basic science view point as to their properties. Specific designs of experiment include: synchrotron-based in situ XRD for phase transition monitoring; gas flow control bench for sensitivity measurement; three-point-bending by AFM for mechanical property measurement. In summary, the electrospinning technique provides a versatile method for synthesizing and assembling 1D nanocomposite structures. The electrospun composite nanofibers showed promising electrical and mechanical properties, which may find applications for gas sensors, reinforced fibrous materials and nano-electrical devices.

  10. Temporal fluctuations in grain size, organic materials and iron concentrations in intertidal surface sediment of San Francisco Bay

    USGS Publications Warehouse

    Thomson-Becker, E. A.; Luoma, S.N.

    1985-01-01

    The physical and chemical characteristics of the oxidized surface sediment in an estuary fluctuate temporally in response to physical forces and apparently-fluctuating inputs. These characteristics, which include grain size and concentrations of organic materials and iron, will influence both trace-metal geochemistry and bioavailability. Temporal trends in the abundance of fine particles, total organic carbon content (TOC), absorbance of extractable organic material (EOM), and concentration of extractable iron in the sediment of San Francisco Bay were assessed using data sets containing approximately monthly samples for periods of two to seven years. Changes in wind velocity and runoff result in monthly changes in the abundance of fine particles in the intertidal zone. Fine-grained particles are most abundant in the late fall/early winter when runoff is elevated and wind velocities are low; particles are coarser in the summer when runoff is low and wind velocities are consistently high. Throughout the bay, TOC is linearly related to fine particle abundance (r = 0.61). Temporal variability occurs in this relationship, as particles are poor in TOC relative to percent of fine particles in the early rainy season. Iron-poor particles also appear to enter the estuary during high runoff periods; while iron is enriched on particle surfaces in the summer. Concentrations of extractable iron and absorbance of EOM vary strongly from year to year. Highest absorbances of EOM occurred in the first year following the drought in 1976-77, and in 1982 and 1983 when river discharge was unusually high. Extractable-iron concentrations were also highest in 1976-77, but were very low in 1982 and 1983. ?? 1985 Dr W. Junk Publishers.

  11. Inorganic and organic fertilizers impact the abundance and proportion of antibiotic resistance and integron-integrase genes in agricultural grassland soil.

    PubMed

    Nõlvak, Hiie; Truu, Marika; Kanger, Kärt; Tampere, Mailiis; Espenberg, Mikk; Loit, Evelin; Raave, Henn; Truu, Jaak

    2016-08-15

    Soil fertilization with animal manure or its digestate may facilitate an important antibiotic resistance dissemination route from anthropogenic sources to the environment. This study examines the effect of mineral fertilizer (NH4NO3), cattle slurry and cattle slurry digestate amendment on the abundance and proportion dynamics of five antibiotic resistance genes (ARGs) and two classes of integron-integrase genes (intI1 and intI2) in agricultural grassland soil. Fertilization was performed thrice throughout one vegetation period. The targeted ARGs (sul1, tetA, blaCTX-M, blaOXA2 and qnrS) encode resistance to several major antibiotic classes used in veterinary medicine such as sulfonamides, tetracycline, cephalosporins, penicillin and fluoroquinolones, respectively. The non-fertilized grassland soil contained a stable background of tetA, blaCTX-M and sul1 genes. The type of applied fertilizer significantly affected ARGs and integron-integrase genes abundances and proportions in the bacterial community (p<0.001 in both cases), explaining 67.04% of the abundance and 42.95% of the proportion variations in the grassland soil. Both cattle slurry and cattle slurry digestate proved to be considerable sources of ARGs, especially sul1, as well as integron-integrases. Sul1, intI1 and intI2 levels in grassland soil were elevated in response to each organic fertilizer's application event, but this increase was followed by a stage of decrease, suggesting that microbes possessing these genes were predominantly entrained into soil via cattle slurry or its digestate application and had somewhat limited survival potential in a soil environment. However, the abundance of these three target genes did not decrease to a background level by the end of the study period. TetA was most abundant in mineral fertilizer treated soil and blaCTX-M in cattle slurry digestate amended soil. Despite significantly different abundances, the abundance dynamics of bacteria possessing these genes were

  12. Organic Photovoltaic Cells: Engineering of the Interfaces Electrodes/Organic Material

    NASA Astrophysics Data System (ADS)

    Bernède, J. C.

    2011-10-01

    The power conversion efficiency (PCE) of organic photovoltaic cells (OPV) depends of the efficiency of four steps, exciton generation by light absorption, exciton diffusion to an electron donor/electron acceptor (ED/EA) interface, charge separation giving free holes and electrons and finally, carrier transport and collection. Therefore, in OPV, besides good photoactive materials, the properties of the interfaces between the organic layers and the electrodes are crucial for achieving high carrier collection efficiency and high PCE. Optoelectronic devices require at least one transparent electrode, usually a transparent conductive oxide (TCO). Electrode contacts play a critical role in determining the device efficiencies. Rates of charge collection at the electrodes must be fast and selective. Contact selectivity is often achieved using buffer interlayers interposed between the electrodes and the organic materials. Efficiency of OPV cells, based on organic donor/acceptor heterojunctions can be strongly improved when the transparent conductive anode, is covered by an anode buffer layer (ABL). Currently, indium-tin oxide (ITO) is the most widely used transparent electrode for organic optoelectronic. Here, the effects of different ABLs (0.5 nm of Au, 3 to 4 nm of MoO3 or CuI) onto the ITO anode are studied using electron donors with different HOMO and LUMO levels. The results indicate that a good matching between the work function, of the anode and the HOMO of the organic electron donor, and the value of the anode surface energy, are important factors for an efficient hole transfer. General rules on the ABL efficiency can be deduced from this study.

  13. Morphology characterization of organic solar cell materials and blends

    NASA Astrophysics Data System (ADS)

    Roehling, John Daniel

    The organization of polymers and fullerenes, both in their pure states and mixed together, have a large impact on their macroscopic properties. For mixtures used in organic solar cells, the morphology of the mixture has a very large impact upon the mixture's ability to efficiently convert sunlight into useful electrical energy. Understanding how the morphology can change under certain processing conditions and in turn, affect the characteristics of the solar cell is therefore important to improving the function of organic solar cells. Conventional poly(3-hexylthiophene):phenyl-C61-butyric acid methyl ester (P3HT:PCBM) solar cells have served as a staple system to study organic solar cell function for nearly a decade. Much of the understanding of how to make these "poorly"conductive organic materials efficiently convert sunlight into electricity has come from the study of P3HT:PCBM. It has long been understood that in order for a polymer:fullerene (electron donor and acceptor, respectively) mixture to function well as a solar cell, two major criteria for the morphology must be met; first, the interface between the two materials must be large to efficiently create charges, and secondly, there must be continous pathways through the "pure" materials for charges to be efficiently collected at the electrodes. This makes it advantageous for OPV materials to phase-separate into interconnected domains with very small domain sizes, a structure that P3HT:PCBM seems to naturally self-assemble. Despite P3HT:PCBM's ability to reach an optimal morphology, a complete understanding of exactly how the morphology affects device performance has not been realized. Completely different morphological models can end up predicting the same device performance characteristics. Much of the problem comes from the assumed morphology within a particular model, which can often be incorrect. The problem lies in the fact that obtaining real, accurate morphological information is difficult. An often

  14. Mineral Associations and Character of Isotopically Anomalous Organic Material in the Tagish Lake Carbonaceous Chondrite

    SciTech Connect

    Zega, T.; Alexander, C; Busemann, H; Nittler, L; Hoppe, P; Stroud, R; Young, A

    2010-01-01

    We report a coordinated analytical study of matrix material in the Tagish Lake carbonaceous chondrite in which the same small ({le}20 {micro}m) fragments were measured by secondary ion mass spectrometry (SIMS), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), electron energy-loss spectroscopy (EELS), and X-ray absorption near-edge spectroscopy (XANES). SIMS analysis reveals H and N isotopic anomalies (hotspots), ranging from hundreds to thousands of nanometers in size, which are present throughout the fragments. Although the differences in spatial resolution of the SIMS techniques we have used introduce some uncertainty into the exact location of the hotspots, in general, the H and N isotopic anomalies are spatially correlated with C enrichments, suggesting an organic carrier. TEM analysis, enabled by site-specific extraction using a focused-ion-beam scanning-electron microscope, shows that the hotspots contain an amorphous component, Fe-Ni sulfides, serpentine, and mixed-cation carbonates. TEM imaging reveals that the amorphous component occurs in solid and porous forms, EDS indicates that it contains abundant C, and EELS and XANES at the C K edge reveal that it is largely aromatic. This amorphous component is probably macromolecular C, likely the carrier of the isotopic anomalies, and similar to the material extracted from bulk samples as insoluble organic matter. However, given the large sizes of some of the hotspots, the disparity in spatial resolution among the various techniques employed in our study, and the phases with which they are associated, we cannot entirely rule out that some of the isotopic anomalies are carried by inorganic material, e.g., sheet silicates. The isotopic composition of the organic matter points to an initially primitive origin, quite possibly within cold interstellar clouds or the outer reaches of the solar protoplanetary disk. The association of organic material with secondary phases, e

  15. Optimization of Organic Solar Cells: Materials, Devices and Interfaces

    NASA Astrophysics Data System (ADS)

    Zhou, Nanjia

    Due to the increasing demand for sustainable clean energy, photovoltaic cells have received intensified attention in the past decade in both academia and industry. Among the types of cells, organic photovoltaic (OPV) cells offer promise as alternatives to conventional inorganic-type solar cells owning to several unique advantages such as low material and fabrication cost. To maximize power conversion efficiencies (PCEs), extensive research efforts focus on frontier molecular orbital (FMO) energy engineering of photoactive materials. Towards this objective, a series of novel donor polymers incorporating a new building block, bithiophene imide (BTI) group are developed, with narrow bandgap and low-lying highest occupied molecular orbital (HOMO) energies to increase short circuit current density, Jsc, and open circuit voltage, Voc.. Compared to other PV technologies, OPVs often suffer from large internal recombination loss and relatively low fill factors (FFs) <70%. Through a combination of materials design and device architecture optimization strategies to improve both microscopic and macroscopic thin film morphology, OPVs with PCEs up to 8.7% and unprecedented FF approaching 80% are obtained. Such high FF are close to those typically achieved in amorphous Si solar cells. Systematic variations of polymer chemical structures lead to understanding of structure-property relationships between polymer geometry and the resulting blend film morphology characteristics which are crucial for achieving high local mobilities and long carrier lifetimes. Instead of using fullerene as the acceptors, an alternative type of OPV is developed employing a high electron mobility polymer, P(NDI2OD-T2), as the acceptor. To improve the all-polymer blend film morphology, the influence of basic solvent properties such as solvent boiling point and solubility on polymer phase separation and charge transport properties is investigated, yielding to a high PCE of 2.7% for all-polymer solar cells

  16. Third- and fifth-order optical nonlinearities in organic materials

    NASA Astrophysics Data System (ADS)

    Said, A. A.; Wamsley, C.; Hagan, D. J.; Van Stryland, E. W.; Reinhardt, Bruce A.; Roderer, Paul; Dillard, Ann G.

    1994-10-01

    We measure the nonlinear optical properties of solutions of a bisbenzethiozole-substituted thiophene compound (BBTDOT) and didecyloxy substituted polyphenyl (DDOS) using the Z-scan technique with 532 nm picosecond pulses. Both compounds exhibit two-photon absorption (2PA) and excited-state absorption (ESA) from the 2PA generated excited states. We measure the magnitude and sign of the real (refractive) and imaginary (2PA) parts of the third-order hyperpolarizability, and the excited-state absorptive and refractive cross sections. We observe third-order self-focusing in BBTDOT and self-defocusing in DDOS while both show excited-state defocusing. All these effects were previously observed and modeled in semiconductors giving insight into the nonlinearities occurring in these organic materials.

  17. Calibrated sulfur isotope abundance ratios of three IAEA sulfur isotope reference materials and V-CDT with a reassessment of the atomic weight of sulfur

    NASA Astrophysics Data System (ADS)

    Ding, T.; Valkiers, S.; Kipphardt, H.; De Bièvre, P.; Taylor, P. D. P.; Gonfiantini, R.; Krouse, R.

    2001-09-01

    Calibrated values have been obtained for sulfur isotope abundance ratios of sulfur isotope reference materials distributed by the IAEA (Vienna). For the calibration of the measurements, a set of synthetic isotope mixtures were prepared gravimetrically from high purity Ag 2S materials enriched in 32S, 33S, and 34S. All materials were converted into SF 6 gas and subsequently, their sulfur isotope ratios were measured on the SF 5+ species using a special gas source mass spectrometer equipped with a molecular flow inlet system (IRMM's Avogadro II amount comparator). Values for the 32S/ 34S abundance ratios are 22.650 4(20), 22.142 4(20), and 23.393 3(17) for IAEA-S-1, IAEA-S-2, and IAEA-S-3, respectively. The calculated 32S/ 34S abundance ratio for V-CDT is 22.643 6(20), which is very close to the calibrated ratio obtained by Ding et al. (1999). In this way, the zero point of the VCDT scale is anchored firmly to the international system of units SI. The 32S/ 33S abundance ratios are 126.942(47), 125.473(55), 129.072(32), and 126.948(47) for IAEA-S-1, IAEA-S-2, IAEA-S-3, and V-CDT, respectively. In this way, the linearity of the V-CDT scale is improved over this range. The values of the sulfur molar mass for IAEA-S-1 and V-CDT were calculated to be 32.063 877(56) and 32.063 911(56), respectively, the values with the smallest combined uncertainty ever reported for the sulfur molar masses (atomic weights).

  18. Developing stable isotopic records from organic material preserved in speleothems

    NASA Astrophysics Data System (ADS)

    Blyth, A.; Baker, A.

    2011-12-01

    Speleothems form excellent archives of environmental change as they are easy to date and preserve multiple environmental records. However, although the stable isotopic composition of speleothem calcite is well characterised, the isotopic composition of organic matter in speleothems has not been investigated in-depth. The approach has considerable potential value in providing isotopic records directly linked to the overlying ecosystem. For stable carbon isotopes, this will provide records independent of the calcite signal, and enable identification of the local primary controls (vegetation type, climate, soil conditions). However, the detailed measurement of isotopic records in speleothem organic matter is hindered by methodological constraints, including extraction of sufficient material, and recovery without adding carbon contamination. Here we present results from a number of methodological techniques and discuss which show most potential for future palaeoenvironmental work. Isotopic records in organic matter can be divided into two main types - analyses of the bulk organic fraction, and compound-specific analyses of molecules of interest (e.g. plant waxes, bacterial lipids etc.). From the point of view of sample size, bulk analysis is the most amenable. Our work shows that TOC in stalagmites can be as low as <0.1 mg/g calcite. However, this is still sufficient to produce bulk organic signals at a sample size of between 100 and 500 mg of calcite powder, which provides a workable temporal resolution at a decadal-centennial scale on many samples. The main obstacle is the recovery of bulk organics without carbon contamination, but whilst avoiding excess acid salts which might damage the instrumentation. One method we propose is the use of an iTOC-CDRS analyser, which measures total organic carbon, and also 12C and 13C isotopes. The approach has the advantage of requiring minimal sample preparation, with drilled powders simply being dissolved in acid. The major

  19. Nanoscale Organic Hybrid Materials (NOHMs) - Structure and Dynamics

    NASA Astrophysics Data System (ADS)

    Archer, Lynden

    2014-03-01

    Polymer-particle composites are used today in virtually every field of technology. When the particles approach nanometer dimensions, large interfacial regions are created in their polymer hosts, which present opportunities and challenges for research, as well as for applications. This talk will focus on a novel class of polymer-particle composite fluids created by densely grafting short organic polymer chains or ionic liquid molecules to inorganic nanostructures. By manipulating the nanoparticle size, polymer molecular weight and surface chemistry, we show that it is possible to create self-suspended suspensions of nanoparticles in which each particle in suspension carries around a discrete share of the suspending medium. The talk will explore consequences of the self-suspended state on fluid structure, rheology, and tethered polymer & particle dynamics in these so-called nanoscale organic hybrid materials (NOHMs). The talk will also discuss particle and tethered polymer dynamics in single-component NOHMs and phase stability, structure, and rheology of NOHMs/polymer blends. This presentation is based on work supported in part by the National Science Foundation, Award No. DMR-1006323.

  20. Conversion and Extraction of Insoluble Organic Materials in Meteorites

    NASA Technical Reports Server (NTRS)

    Locke, Darren R.; Burton, Aaron S.; Niles, Paul B.

    2016-01-01

    We endeavor to develop and implement methods in our laboratory to convert and extract insoluble organic materials (IOM) from low car-bon bearing meteorites (such as ordinary chondrites) and Precambrian terrestrial rocks for the purpose of determining IOM structure and prebiotic chemistries preserved in these types of samples. The general scheme of converting and extracting IOM in samples is summarized in Figure 1. First, powdered samples are solvent extracted in a micro-Soxhlet apparatus multiple times using solvents ranging from non-polar to polar (hexane - non-polar, dichloromethane - non-polar to polar, methanol - polar protic, and acetonitrile - polar aprotic). Second, solid residue from solvent extractions is processed using strong acids, hydrochloric and hydrofluoric, to dissolve minerals and isolate IOM. Third, the isolated IOM is subjected to both thermal (pyrolysis) and chemical (oxidation) degradation to release compounds from the macromolecular material. Finally, products from oxidation and pyrolysis are analyzed by gas chromatography - mass spectrometry (GCMS). We are working toward an integrated method and analysis scheme that will allow us to determine prebiotic chemistries in ordinary chondrites and Precambrian terrestrial rocks. Powerful techniques that we are including are stepwise, flash, and gradual pyrolysis and ruthenium tetroxide oxidation. More details of the integrated scheme will be presented.

  1. Active-Site-Accessible, Porphyrinic Metal;#8722;Organic Framework Materials

    SciTech Connect

    Farha, Omar K.; Shultz, Abraham M.; Sarjeant, Amy A.; Nguyen, SonBinh T.; Hupp, Joseph T.

    2012-02-06

    On account of their structural similarity to cofactors found in many metallo-enzymes, metalloporphyrins are obvious potential building blocks for catalytically active, metal-organic framework (MOF) materials. While numerous porphyrin-based MOFs have already been described, versions featuring highly accessible active sites and permanent microporosity are remarkably scarce. Indeed, of the more than 70 previously reported porphyrinic MOFs, only one has been shown to be both permanently microporous and contain internally accessible active sites for chemical catalysis. Attempts to generalize the design approach used in this single successful case have failed. Reported here, however, is the synthesis of an extended family of MOFs that directly incorporate a variety of metalloporphyrins (specifically Al{sup 3+}, Zn{sup 2+}, Pd{sup 2+}, Mn{sup 3+}, and Fe{sup 3+} complexes). These robust porphyrinic materials (RPMs) feature large channels and readily accessible active sites. As an illustrative example, one of the manganese-containing RPMs is shown to be catalytically competent for the oxidation of alkenes and alkanes.

  2. Micromachining of transparent materials by laser ablation of organic solution

    NASA Astrophysics Data System (ADS)

    Wang, Jun; Niino, Hiroyuki; Yabe, Akira

    2000-11-01

    Transparent materials such as fused silica, quartz, calcium fluoride, and fluorocarbon polymer were etched upon irradiation of organic solution containing pyrene with a conventional KrF excimer laser. Threshold fluence for etching was 240 mJ/cm2 for fused silica. Etch rate remarkably depended on a concentration of pyrene: higher etch rate with the increase of pyrene concentration. It means that pyrene molecules play an important role in this process. The etch rate can be easily controlled through changing a laser pulse number, a laser fluence and a concentration of solution. The mechanism for this process is discussed by cyclic multiphotonic absorption of pyrene in the excited states, thermal relaxation, and formation of super-heated solution. As the results, it is suggested that the process is based on the combination of two processes in the interface between the transparent materials and the liquid: one is a heating process by a super-heated liquid and the other is an attacking process by a high temperature and pressure vapor.

  3. Organic-inorganic planar hybrid materials for spasers

    NASA Astrophysics Data System (ADS)

    Toropov, Nikita A.; Kamalieva, Aisylu N.; Vartanyan, Tigran A.

    2015-05-01

    We strive to obtain highly fluorescent planar materials that may be used for the development of nanolasers based on localized plasmons. The promissing candidates for this purpose are materials consisting of mixtures of organic molecules, polymer, and silver nanoparticles. Silver nanoparticles were preliminary deposited on the quartz substrates. These samples were characterized by SEM and absorption spectroscopy. Then, they were covered by the polymer/rhodamine and polymer/coumarin layers using either spin-coating or evaporation techniques and characterized by confocal luminescent microscopy and spectroscopy. As a result of the localized surface plasmon excitation, we observed the enhancement of the rhodamine and coumarine absorption in the near fields of silver nanoparticles. The fluorescence of the thin films of polymer activated by dyes molecules with silver nanoparticles was almost 20-fold more intense than that on the bare dielectric surfaces without silver nanoparticles. In the presence Ag nanoparticles and at increased intensities of excitation we found also slight narrowing of the luminescence spectrum of polymer/coumarin layers.

  4. Microstructural self-organization in granular materials during failure

    NASA Astrophysics Data System (ADS)

    Hadda, Nejib; Nicot, François; Wan, Richard; Darve, Félix

    2015-02-01

    The present paper is concerned with the analysis of microstructural instabilities in granular materials and with their relation to both macroscopic localized and diffuse failure modes. A discrete-element (DEM) computer simulation of deformations in an idealized two-dimensional frictional particle assembly subject to various biaxial loadings-notably drained compression and proportional strain paths-is proposed as a prototype model to investigate the underlying physics of material failure. Based on the transfer of the second-order work criterion to the microscopic level, we seek for contacts tagged as c- within the granular assembly that undergo instabilities during loading history. The DEM computations yield a description of failure as a microstructural self-organization process by which c- contacts aggregate into clusters which can either grow or breakdown as the network of contacts adjusts itself to externally applied loads during deformation history. It is proposed here that there is a close relation between the clustering of c- contacts and the resulting failure mode based on cluster size and spatial distribution. Localized deformations are found to correlate well with sustained growth of the above clusters, while diffuse failure has more to do with smaller clusters experiencing suppressed development. A comprehensive statistical analysis on the clusters lends support to this conclusion.

  5. Organic hydrogels as potential sorbent materials for water purification

    NASA Astrophysics Data System (ADS)

    Linardatos, George; Bekiari, Vlasoula; Bokias, George

    2014-05-01

    Hydrogels are three-dimensional, hydrophilic, polymeric networks capable to adsorb large amounts of water or biological fluids. The networks are composed of homopolymers or copolymers and are insoluble due to the presence of chemical or physical cross-links. Depending on the nature of the structural units, swelling or shrinking of these gels can be activated by several external stimuli, such as solvent, heat, pH, electric stimuli. As a consequence, these materials are attractive for several applications in a variety of fields: drug delivery, muscle mimetic soft linear actuators, hosts of nanoparticles and semiconductors, regenerative medicine etc. Of special interest is the application of hydrogels for water purification, since they can effectively adsorb several water soluble pollutants such as metal ions, inorganic or organic anions, organic dyestaff, etc. In the present work, anionic hydrogels bearing negatively charged -COO- groups were prepared and investigated. These are based on the anionic monomer sodium acrylate (ANa) and the nonionic one N,N-dimethylacrylamide (DMAM). A series of copolymeric hydrogels (P(DMAM-co-ANax) were synthesized. The molar content x of ANa units (expressing the molar charged content of the hydrogel) varies from 0 (nonionic poly(N,N-dimethylacrylamide), PDMAM, hydrogel) up to 1 (fully charged poly(sodium acrylate), PANa, hydrogel). The hydrogels were used to extract organic or inorganic solutes from water. Cationic and anionic model dyes, as well as multivalent inorganic ions, have been studied. It is found that cationic dyes are strongly adsorbed and retained by the hydrogels, while adsorbance of anionic dyes was negligible. Both maximum adsorption and equilibrium binding constant depend on the chemical structure of the dye, the presence of functional chemical groups and the hydrophobic-hydrophilic balance. In the case of metal cations, adsorption depends mostly on the charge of the cation. In addition, crucial factors controlling

  6. Organics on Mars: Laboratory studies of organic material under simulated martian conditions

    NASA Astrophysics Data System (ADS)

    ten Kate, Inge Loes

    2006-01-01

    The search for organic molecules and traces of life on Mars has been a major topic in planetary science for several decades, and is the future perspective of several missions to Mars. In order to determine where and what those missions should be looking for, laboratory experiments under simulated Mars conditions have been performed. This thesis describes the effects of simulated martian surface conditions on organic material (amino acids) and living organisms (halophilic archaea). Experiments have been performed to study the stability of thin films of glycine and alanine against UV irradiation under different conditions. Thin films of glycine and alanine have a half-life of 22 ± 5 hours and 3 ± 1 hours, respectively, when extrapolated to Mars-like UV flux levels in vacuum. The presence of a 7 mbar CO2 atmosphere does not affect these destruction rates. Cooling the thin films to 210 K (average Mars temperature) lowers the destruction rate by a factor of 7. The intrinsic amino acid composition of two martian soil analogues, JSC Mars-1 and Salten Skov, has been investigated. The results demonstrated that these analogues are inappropriate for a life-science study in their raw state. Besides amino acids, the response of the halophilic archaea Natronorubrum sp. strain HG-1 to Mars-like conditions, such as low pressure, UV radiation and low temperatures, has been studied. From the results we concluded that this strain would not be a good model organism to survive on the surface of Mars.

  7. Molecular organic crystalline matrix for hybrid organic-inorganic (nano) composite materials

    NASA Astrophysics Data System (ADS)

    Stanculescu, A.; Tugulea, L.; Alexandru, H. V.; Stanculescu, F.; Socol, M.

    2005-02-01

    Metal-doped benzil crystals have been grown by thermal gradient solidification in a vertical transparent growth configuration to investigate the effect of metallic guest on the ordered organic host. We have identified the conditions for growing homogeneous, optically good crystals of benzil doped with sodium and silver, limiting the effect of supercooling, low thermal conductivity and anisotropy of the growth speed (temperature gradient at the liquid-solid interface: 10-25 °C, moving speed of the growth interface 2.0 mm/h). The nature and concentration of the dopant are parameters affecting, through the growth process, the crystalline perfection and the optical properties of the organic matrix. Bulk optical characterisation, by spectrophotometrical methods, has offered details on some intrinsic properties of the system metal particles/benzil crystalline matrix. Analytical processing of the experimental data emphasised that benzil is a wide optical band gap organic semiconductor Eg=2.65 eV. We also have investigated the effect of sodium and silver on the properties of benzil crystal as potential transparent semiconductor matrix for (nano)composite metal/molecular organic material. With the increase of sodium concentration from c=1 to 6 wt%, a small narrowing of the band gap has been remarked. The same behaviour has been found for benzil doped with silver (c=2 wt%) compared to pure benzil.

  8. Organic/inorganic interfaced field-effect transistor properties with a novel organic semiconducting material

    NASA Astrophysics Data System (ADS)

    Demir, Ahmet; Atahan, Alparslan; Bağcı, Sadık; Aslan, Metin; Saif Islam, M.

    2016-01-01

    A novel 1,3,4-oxadiazole-substituted benzo[b]triphenylene was synthesized by three-step synthetic procedure and OFET device design was successfully designed after theoretical calculations made using Gaussian software. For investigating the field-effect properties of designed organic electronic device, a SiO2 (300 nm) was thermally grown on p-Si wafer at 1000 °C as a dielectric layer and gate, source and drain contacts have been deposited using Au metal with physical vapour deposition. 1,3,4-Oxadiazole-substituted benzo[b]triphenylene was spin coated on the source and drain electrodes of our device, forming organic/inorganic interfaced field-effect transistors. Surface morphology and thin film properties were investigated using AFM. All electrical measurements were done in air ambient. The device showed a typical p-type channel behaviour with increasing negative gate bias voltage values. Our results have surprisingly shown that the saturation regime of this device has high mobility (μFET), excellent on/off ratio (Ion/Ioff), high transconductance (gm) and a small threshold voltage (VTh). The values of μFET, Ion/Ioff, gm and VTh were found as 5.02 cm2/Vs, 0.7 × 103, 5.64 μS/mm and 1.37 V, respectively. These values show that our novel organic material could be a potential candidate for organic electronic device applications in the future.

  9. Seasonal relationships between planktonic microorganisms and dissolved organic material in an alpine stream

    USGS Publications Warehouse

    McKnight, Diane M.; Smith, R.L.; Harnish, R.A.; Miller, C.L.; Bencala, K.E.

    1993-01-01

    The relationships between the abundance and activity of planktonic, heterotrophic microorganisms and the quantity and characteristics of dissolved organic carbon (DOC) in a Rocky Mountain stream were evaluated. Peak values of glucose uptake, 2.1 nmol L-1 hr-1, and glucose concentration, 333 nM, occurred during spring snowmelt when the water temperature was 4.0??C and the DOC concentration was greatest. The turnover time of the in situ glucose pool ranged seasonally from 40-1110 hours, with a mean of 272 hr. Seasonal uptake of3H-glucose, particulate ATP concentrations, and direct counts of microbial biomass were independent of temperature, but were positively correlated with DOC concentrations and negatively correlated with stream discharge. Heterotrophic activity in melted snow was generally low, but patchy. In the summer, planktonic heterotrophic activity and microbial biomass exhibited small-scale diel cycles which did not appear to be related to fluctuations in discharge or DOC, but could be related to the activity of benthic invertebrates. Leaf-packs placed under the snow progressively lost weight and leachable organic material during the winter, indicating that the annual litterfall in the watershed may be one source of the spring flush of DOC. These results indicate that the availability of labile DOC to the stream ecosystem is the primary control on seasonal variation in heterotrophic activity of planktonic microbial populations. ?? 1993 Kluwer Academic Publishers.

  10. Inorganic-organic electrolyte materials for energy applications

    NASA Astrophysics Data System (ADS)

    Fei, Shih-To

    This thesis research is devoted to the development of phosphazene-based electrolyte materials for use in various energy applications. Phosphazenes are inorganic-organic materials that provide unusal synthetic advantages and unique process features that make them useful in energy research. This particular thesis consists of six chapters and is focused on four specific aspects: lithium battery, solar cell, and fuel cell electrolytes, and artificial muscles. Chapter 1 is written as an introduction and review of phosphazene electrolytes used in energy applications. In this introduction the basic history and characteristics of the phosphazenes are discussed briefly, followed by examples of current and future applications of phosphazene electrolytes related to energy. Notes are included on how the rest of the chapters relate to previous work. Chapters 2 and 3 discuss the conductivity and fire safety of ethyleneoxy phosphazene gel electrolytes. The current highly flammable configurations for rechargeable lithium batteries generate serious safety concerns. Although commercial fire retardant additives have been investigated, they tend to decrease the overall efficiency of the battery. In these two chapters the discussion is focused on ionically conductive, non-halogenated lithium battery additives based on a methoxyethoxyethoxyphosphazene oligomer and the corresponding high polymer, both of which can increase the fire resistance of a battery while retaining a high energy efficiency. Conductivities in the range of 10 -4 Scm-1 have been obtained for self-extinguishing, ion-conductive methoxyethoxyethoxyphosphazene oligomers. The addition of 25 wt% high polymeric poly[bis(methoxyethoxyethoxy)phosphazene] to propylene carbonate electrolytes lowers the flammability by 90% while maintaining a good ionic conductivity of 2.5x10--3 Scm -1 Chapter 2 is focused more on the electrochemical properties of the electrolytes and how they compare to other similar materials, while Chapter 3

  11. The secondary history of Sutter's Mill CM carbonaceous chondrite based on water abundance and the structure of its organic matter from two clasts

    NASA Astrophysics Data System (ADS)

    Beck, P.; Quirico, E.; Garenne, A.; Yin, Q.-Z.; Bonal, L.; Schmitt, B.; Montes-Hernandez, G.; Montagnac, G.; Chiriac, R.; Toche, F.

    2014-11-01

    Sutter's Mill is a regolith breccia composed of both heavily altered clasts and more reduced xenoliths. Here, we present a detailed investigation of fragments of SM18 and SM51. We have characterized the water content and the mineralogy by infrared (IR) and thermogravimetric analysis (TGA) and the structure of the organic compounds by Raman spectroscopy, to characterize the secondary history of the clasts, including aqueous alteration and thermal metamorphism. The three methods used in this study suggest that SM18 was significantly heated. The amount of water contained in phyllosilicates derived by TGA is estimated to be approximately 3.2 wt%. This value is quite low compared with other CM chondrites that typically range from 6 to 12 wt%. The infrared transmission spectra of SM18 show that the mineralogy of the sample is dominated by a mixture of phyllosilicate and olivine. SM18 shows an intense peak at 11.2 μm indicative of olivine (Fig. 1). If we compare SM18 with other CM and metamorphosed CM chondrites, it shows one of the most intense olivine signatures, and therefore a lower proportion of phyllosilicate minerals. The Raman results tend to support a short-duration heating hypothesis. In the ID/IG versus FWHM-D diagram, SM18 appears to be unusual compared to most CM samples, and close to the metamorphosed CM chondrites Pecora Escarpment (PCA) 91008 and PCA 02012. In the case of SM51, infrared spectroscopy reveals that olivine is less abundant than in SM18 and the 10 μm silicate feature is more similar to that of moderately altered CM chondrites (like Murchison or Queen Alexandra Range [QUE] 97990). Raman spectroscopy does not clearly point to a heating event for SM51 in the ID/IG versus FWHM-D diagram. However, TGA analysis suggests that SM51 was slightly dehydrated as the amount of water contained in phyllosilicates is approximately 3.7 wt%, which is higher than SM18, but still lower than phyllosilicate water contents in weakly altered CM chondrites

  12. Ecotoxicity of selected nano-materials to aquatic organisms.

    PubMed

    Blaise, C; Gagné, F; Férard, J F; Eullaffroy, P

    2008-10-01

    Present knowledge concerning the ecotoxic effects of nano-materials is very limited and merits to be documented more fully. For this purpose, we appraised the toxicity of nine metallic nano-powders (copper zinc iron oxide, nickel zinc iron oxide, yttrium iron oxide, titanium dioxide, strontium ferrite, indium tin oxide, samarium oxide, erbium oxide, and holmium oxide) and of two organic nano- powders (fullerene-C60 and single-walled carbon nanotube or SWCNT). After a simple process where nano-powders (NPs) were prepared in aqueous solution and filtered, they were then bioassayed across several taxonomic groups including decomposers (bacteria), primary producers (micro-algae), as well as primary and secondary consumers (micro-invertebrates and fish). Toxicity data generated on the 11 NPs reflected a wide spectrum of sensitivity that was biological level-, test-, and endpoint-specific. With all acute and chronic tests confounded for these 11 NPs, toxicity responses spanned over three orders of magnitude: >463 mg/L (24 h LC50 of the invertebrate Thamnoplatyurus platyurus for fullerene-C60) / 0.3 mg/L (96 h EC50 of the invertebrate Hydra attenuata for indium tin oxide), that is a ratio of 1543. On the basis of the MARA (Microbial Array for Risk Assessment) assay toxic fingerprint concept, it is intimated that NPs may have different modes of toxic action. When mixed in a 1:1 ratio with a certified reference material (CRM) sediment, two solid phase assays and an elutriate assay, respectively, showed that five NPs (copper zinc iron oxide, samarium oxide, erbium oxide, holmium oxide, and SWCNT) were able to increase both CRM sediment toxicity and its elutriate toxicity. This initial investigation suggests that chemicals emerging from nanotechnology may pose a risk to aquatic life in water column and sediment compartments and that further studies on their adverse effects are to be encouraged. PMID:18528913

  13. Supramolecularly self-organized nanomaterials: A voyage from inorganic particles to organic light-harvesting materials

    NASA Astrophysics Data System (ADS)

    Varotto, Alessandro

    In 2009 the U.S. National Science Foundation announced the realignment of the Chemistry Divisions introducing the new interdisciplinary program of "Macromolecular, Supramolecular and Nanochemistry." This statement officially recognizes a field of studies that has already seen the publication of many thousands of works in the past 20 years. Nanotechnology and supramolecular chemistry can be found in the most diverse disciplines, from biology to engineering, to physics. Furthermore, many technologies rely on nanoscale dimensions for more than one component. Nanomaterials and technologies are on the market with a range of applications from composite materials, to electronics, to medicine, to sensing and more. This thesis will introduce a variety of studies and applications of supramolecular chemistry to form nanoscale photonic materials from soft matter. We will first illustrate a method to synthesize metallic nanoparticles using plasmids DNA as a mold. The circular DNA functions as a sacrificial template to shape the particles into narrowly monodispersed nanodiscs. Secondly, we will describe the synthesis of a highly fluorinated porphyrin derivative and how the fluorines improve the formation of ultra thin films when the porphyrin is blended with fullerene C60. Finally, we will show how to increase the short-circuit current in a solar cell built with an internal parallel tandem light harvesting design. A blend of phthalocyanines, each with a decreasing optical band gap, is supramolecularly self-organized with pyridyl-C60 within thin films. The different band gaps of the single phthalocyanines capture a wider segment of the solar spectrum increasing the overall efficiency of the device. In conclusion, we have presented a number of studies for the preparation of inorganic and organic nanomaterials and their application in supramolecularly organized photonic devices.

  14. Computational Design of Photovoltaic Materials with Self Organized Nano Structures

    NASA Astrophysics Data System (ADS)

    Sato, Kazunori; Katayama-Yoshida, Hiroshi

    2013-03-01

    Chalcopyrite and II-VI semiconductors, such as Cu(In, Ga)Se2, Cu2ZnSn(S, Se)4 and Cd(S, Te), are one of the most promising materials for low cost photovoltaic solar-cells. In this paper, based on first-principles calculations, we propose that self-organized nano-structures in these compounds will enhance the conversion efficiency. Our calculations are based on the KKR-CPA-LDA with the self-interaction correction. We also use VASP package for calculating mixing energy and effective interactions of the systems by using the cluster expansion method. For phase separating systems, we simulate nano-structure formation by using the Monte Carlo method. It is expected that the photo-generated electron-hole pairs are efficiently separated by the type-II interface and then effectively transferred along the quasi-one-dimensional structures. Moreover, we can expect multiplication of generated carriers due to the multi-exciton effects in nano-structures.

  15. Impact of plasma exposure on organic low-k materials

    NASA Astrophysics Data System (ADS)

    Smirnov, E.; Ferchichi, A. K.; Huffman, C.; Baklanov, M. R.

    2010-02-01

    The impact of different etch plasmas on advanced porous organic low-k material is studied. Several analytical techniques such as Ellipsometric porosimetry (porosity and pore size), Water Contact Angle (hydrophilicity) and FTIR spectroscopy (chemical composition) are used for evaluation. The wafers were exposed in three different chambers (ICP, CCP and μWave) with various gas mixtures. The highest etch rate is obtained in O2/Cl2 and H2/N2 plasma in an inductively coupled plasma (ICP chamber) and the capacitevly coupled plasma (CCP chamber) respectively. Exposure of the low-k films in CCP plasma chamber with C4F8 / CH2F2 / Ar/N2 gas mixture can be used for the further damage prevention, because completely seals the pores. The surface of the sealed films remains hydrophobic (WCA=88°). The He/H2, C4F8/CH2F2/O2/Ar/N2, CF4/CH2F2 gas mixtures in CCP chamber provide partial pore sealing. The measured refractive indices showed no significant change between the damaged and pristine samples, however the plasma exposure in O2/Cl2 shows a tendency of C=O groups formation which may act as further centers of moisture adsorption.

  16. The potential of organic polymer-based hydrogen storage materials.

    PubMed

    Budd, Peter M; Butler, Anna; Selbie, James; Mahmood, Khalid; McKeown, Neil B; Ghanem, Bader; Msayib, Kadhum; Book, David; Walton, Allan

    2007-04-21

    The challenge of storing hydrogen at high volumetric and gravimetric density for automotive applications has prompted investigations into the potential of cryo-adsorption on the internal surface area of microporous organic polymers. A range of Polymers of Intrinsic Microporosity (PIMs) has been studied, the best PIM to date (a network-PIM incorporating a triptycene subunit) taking up 2.7% H(2) by mass at 10 bar/77 K. HyperCrosslinked Polymers (HCPs) also show promising performance as H(2) storage materials, particularly at pressures >10 bar. The N(2) and H(2) adsorption behaviour at 77 K of six PIMs and a HCP are compared. Surface areas based on Langmuir plots of H(2) adsorption at high pressure are shown to provide a useful guide to hydrogen capacity, but Langmuir plots based on low pressure data underestimate the potential H(2) uptake. The micropore distribution influences the form of the H(2) isotherm, a higher concentration of ultramicropores (pore size <0.7 nm) being associated with enhanced low pressure adsorption. PMID:17415491

  17. Centrosomes are autocatalytic droplets of pericentriolar material organized by centrioles

    NASA Astrophysics Data System (ADS)

    Zwicker, David; Decker, Markus; Jaensch, Steffen; Hyman, Anthony A.; Jülicher, Frank

    2014-03-01

    We propose a physical description of the centrosome, a membrane-less organelle involved in cell division. In our model, centrosome material occurs in a soluble form in the cytosol and a form that tends to undergo phase separation from the cytosol. We find that an autocatalytic chemical transition between these forms accounts for the temporal evolution observed in experiments. Interestingly, the nucleation of centrosomes can be controlled by an enzymatic activity of the centrioles, which are present at the core of all centrosomes. This non-equilibrium feature also allows for multiple stable centrosomes, a situation which is unstable in equilibrium phase separation. Our theory explains the growth dynamics of centrosomes for all cell sizes down to the eight-cell stage of the C. elegans embryo. It also accounts for data acquired in experiments with aberrant numbers of centrosomes and altered cell volumes. Furthermore, our model can describe unequal centrosome sizes observed in cells with disturbed centrioles. Our example suggests a general picture of the organization of membrane-less organelles.

  18. Development of polyatomic ion beam system using liquid organic materials

    NASA Astrophysics Data System (ADS)

    Takaoka, G. H.; Nishida, Y.; Yamamoto, T.; Kawashita, M.

    2005-08-01

    We have developed a new type of polyatomic ion beam system using liquid organic materials such as octane and ethanol, which consists of a capillary type of nozzle, an ionizer, a mass-separator and a substrate holder. Ion current extracted after ionization was 430 μA for octane and 200 μA for ethanol, respectively. The mass-analysis was realized using a compact E × B mass filter, and the mass-analyzed ion beams were transferred toward the substrate. The ion current density at the substrate was a few μA/cm2 for the mass-separated ion species. Interactions of polyatomic ion beams with silicon (Si) surfaces were investigated by utilizing the ellipsometry measurement. It was found that the damaged layer thickness irradiated by the polyatomic ions with a mass number of about 40 was smaller than that by Ar ion irradiation at the same incident energy and ion fluence. The result indicated that the rupture of polyatomic ions occurred upon its impact on the Si surface with an incident energy larger than a few keV. In addition, the chemical modification of Si surfaces such as wettability could be achieved by adjusting the incident energy for the ethanol ions, which included all the fragment ions.

  19. Centrosomes are autocatalytic droplets of pericentriolar material organized by centrioles

    PubMed Central

    Zwicker, David; Decker, Markus; Jaensch, Steffen; Hyman, Anthony A.; Jülicher, Frank

    2014-01-01

    Centrosomes are highly dynamic, spherical organelles without a membrane. Their physical nature and their assembly are not understood. Using the concept of phase separation, we propose a theoretical description of centrosomes as liquid droplets. In our model, centrosome material occurs in a form soluble in the cytosol and a form that tends to undergo phase separation from the cytosol. We show that an autocatalytic chemical transition between these forms accounts for the temporal evolution observed in experiments. Interestingly, the nucleation of centrosomes can be controlled by an enzymatic activity of the centrioles, which are present at the core of all centrosomes. This nonequilibrium feature also allows for multiple stable centrosomes, a situation that is unstable in equilibrium phase separation. Our theory explains the growth dynamics of centrosomes for all cell sizes down to the eight-cell stage of the Caenorhabditis elegans embryo, and it also accounts for data acquired in experiments with aberrant numbers of centrosomes and altered cell volumes. Furthermore, the model can describe unequal centrosome sizes observed in cells with perturbed centrioles. We also propose an interpretation of the molecular details of the involved proteins in the case of C. elegans. Our example suggests a general picture of the organization of membraneless organelles. PMID:24979791

  20. Spatiotemporal variations in the abundance and composition of bulk and chromophoric dissolved organic matter in seasonally hypoxia-influenced Green Bay, Lake Michigan, USA.

    PubMed

    DeVilbiss, Stephen E; Zhou, Zhengzhen; Klump, J Val; Guo, Laodong

    2016-09-15

    Green Bay, Lake Michigan, USA, is the largest freshwater estuary in the Laurentian Great Lakes and receives disproportional terrestrial inputs as a result of a high watershed to bay surface area ratio. While seasonal hypoxia and the formation of "dead zones" in Green Bay have received increasing attention, there are no systematic studies on the dynamics of dissolved organic matter (DOM) and its linkage to the development of hypoxia. During summer 2014, bulk dissolved organic carbon (DOC) analysis, UV-vis spectroscopy, and fluorescence excitation-emission matrices (EEMs) coupled with PARAFAC analysis were used to quantify the abundance, composition and source of DOM and their spatiotemporal variations in Green Bay, Lake Michigan. Concentrations of DOC ranged from 202 to 571μM-C (average=361±73μM-C) in June and from 279 to 610μM-C (average=349±64μM-C) in August. In both months, absorption coefficient at 254nm (a254) was strongly correlated to bulk DOC and was most abundant in the Fox River, attesting a dominant terrestrial input. Non-chromophoric DOC comprised, on average, ~32% of bulk DOC in June with higher terrestrial DOM and ~47% in August with higher aquagenic DOM, indicating that autochthonous and more degraded DOM is of lower optical activity. PARAFAC modeling on EEM data resulted in four major fluorescent DOM components, including two terrestrial humic-like, one aquagenic humic-like, and one protein-like component. Variations in the abundance of DOM components further supported changes in DOM sources. Mixing behavior of DOM components also indicated that while bulk DOM behaved quasi-conservatively, significant compositional changes occurred during transport from the Fox River to the open bay. PMID:27243792

  1. Robust and Porous β-Diketiminate-Functionalized Metal-Organic Frameworks for Earth-Abundant-Metal-Catalyzed C-H Amination and Hydrogenation.

    PubMed

    Thacker, Nathan C; Lin, Zekai; Zhang, Teng; Gilhula, James C; Abney, Carter W; Lin, Wenbin

    2016-03-16

    We have designed a strategy for postsynthesis installation of the β-diketiminate (NacNac) functionality in a metal-organic framework (MOF) of UiO-topology. Metalation of the NacNac-MOF (I) with earth-abundant metal salts afforded the desired MOF-supported NacNac-M complexes (M = Fe, Cu, and Co) with coordination environments established by detailed EXAFS studies. The NacNac-Fe-MOF catalyst, I•Fe(Me), efficiently catalyzed the challenging intramolecular sp(3) C-H amination of a series of alkyl azides to afford α-substituted pyrrolidines. The NacNac-Cu-MOF catalyst, I•Cu(THF), was effective in promoting the intermolecular sp(3) C-H amination of cyclohexene using unprotected anilines to provide access to secondary amines in excellent selectivity. Finally, the NacNac-Co-MOF catalyst, I•Co(H), was used to catalyze alkene hydrogenation with turnover numbers (TONs) as high as 700 000. All of the NacNac-M-MOF catalysts were more effective than their analogous homogeneous catalysts and could be recycled and reused without a noticeable decrease in yield. The NacNac-MOFs thus provide a novel platform for engineering recyclable earth-abundant-element-based single-site solid catalysts for many important organic transformations. PMID:26885768

  2. Flexible n-type thermoelectric materials by organic intercalation of layered transition metal dichalcogenide TiS2.

    PubMed

    Wan, Chunlei; Gu, Xiaokun; Dang, Feng; Itoh, Tomohiro; Wang, Yifeng; Sasaki, Hitoshi; Kondo, Mami; Koga, Kenji; Yabuki, Kazuhisa; Snyder, G Jeffrey; Yang, Ronggui; Koumoto, Kunihito

    2015-06-01

    Organic semiconductors are attracting increasing interest as flexible thermoelectric materials owing to material abundance, easy processing and low thermal conductivity. Although progress in p-type polymers and composites has been reported, their n-type counterpart has fallen behind owing to difficulties in n-type doping of organic semiconductors. Here, we present an approach to synthesize n-type flexible thermoelectric materials through a facile electrochemical intercalation method, fabricating a hybrid superlattice of alternating inorganic TiS2 monolayers and organic cations. Electrons were externally injected into the inorganic layers and then stabilized by organic cations, providing n-type carriers for current and energy transport. An electrical conductivity of 790 S cm(-1) and a power factor of 0.45 mW m(-1) K(-2) were obtained for a hybrid superlattice of TiS2/[(hexylammonium)x(H2O)y(DMSO)z], with an in-plane lattice thermal conductivity of 0.12 ± 0.03 W m(-1) K(-1), which is two orders of magnitude smaller than the thermal conductivities of the single-layer and bulk TiS2. High power factor and low thermal conductivity contributed to a thermoelectric figure of merit, ZT, of 0.28 at 373 K, which might find application in wearable electronics. PMID:25849369

  3. A Review of Patterned Organic Bioelectronic Materials and their Biomedical Applications.

    PubMed

    Park, SooHyun; Kang, You Jung; Majd, Sheereen

    2015-12-01

    Organic electronic materials are rapidly emerging as superior replacements for a number of conventional electronic materials, such as metals and semiconductors. Conducting polymers, carbon nanotubes, graphenes, organic light-emitting diodes, and diamond films fabricated via chemical vapor deposition are the most popular organic bioelectronic materials that are currently under active research and development. Besides the capability to translate biological signals to electrical signals or vice versa, organic bioelectronic materials entail greater biocompatibility and biodegradability compared to conventional electronic materials, which makes them more suitable for biomedical applications. When patterned, these materials bring about numerous capabilities to perform various tasks in a more-sophisticated and high-throughput manner. Here, we provide an overview of the unique properties of organic bioelectronic materials, different strategies applied to pattern these materials, and finally their applications in the field of biomedical engineering, particularly biosensing, cell and tissue engineering, actuators, and drug delivery. PMID:26397962

  4. Viscosity of α-pinene secondary organic material and implications for particle growth and reactivity.

    PubMed

    Renbaum-Wolff, Lindsay; Grayson, James W; Bateman, Adam P; Kuwata, Mikinori; Sellier, Mathieu; Murray, Benjamin J; Shilling, John E; Martin, Scot T; Bertram, Allan K

    2013-05-14

    Particles composed of secondary organic material (SOM) are abundant in the lower troposphere. The viscosity of these particles is a fundamental property that is presently poorly quantified yet required for accurate modeling of their formation, growth, evaporation, and environmental impacts. Using two unique techniques, namely a "bead-mobility" technique and a "poke-flow" technique, in conjunction with simulations of fluid flow, the viscosity of the water-soluble component of SOM produced by α-pinene ozonolysis is quantified for 20- to 50-μm particles at 293-295 K. The viscosity is comparable to that of honey at 90% relative humidity (RH), similar to that of peanut butter at 70% RH, and at least as viscous as bitumen at ≤30% RH, implying that the studied SOM ranges from liquid to semisolid or solid across the range of atmospheric RH. These data combined with simple calculations or previous modeling studies are used to show the following: (i) the growth of SOM by the exchange of organic molecules between gas and particle may be confined to the surface region of the particles for RH ≤ 30%; (ii) at ≤30% RH, the particle-mass concentrations of semivolatile and low-volatility organic compounds may be overpredicted by an order of magnitude if instantaneous equilibrium partitioning is assumed in the bulk of SOM particles; and (iii) the diffusivity of semireactive atmospheric oxidants such as ozone may decrease by two to five orders of magnitude for a drop in RH from 90% to 30%. These findings have possible consequences for predictions of air quality, visibility, and climate. PMID:23620520

  5. Viscosity of α-pinene secondary organic material and implications for particle growth and reactivity

    SciTech Connect

    Renbaum-Wolff, Lindsay; Grayson, James W.; Bateman, Adam P.; Kuwata, Mikinori; Sellier, Mathieu; Murray, Benjamin J.; Shilling, John E.; Martin, Scot T.; Bertram, Allan K.

    2013-05-14

    Particles composed of secondary organic material (SOM) are abundant in the lower troposphere and play important roles in climate, air quality, and health. The viscosity of these particles is a fundamental property that is presently poorly quantified for conditions relevant to the lower troposphere. Using two new techniques, namely a bead-mobility technique and a poke-flow technique, in conjunction with simulations of fluid flow, we measure the viscosity of the watersoluble component of SOM produced by α-pinene ozonolysis. The viscosity is comparable to that of honey at 90% relative humidity (RH), comparable to that of peanut butter at 70% RH and greater than or comparable to that of bitumen for ≤ 30% RH, implying that the studied SOM ranges from liquid to semisolid/solid at ambient relative humidities. With the Stokes-Einstein relation, the measured viscosities further imply that the growth and evaporation of SOM by the exchange of organic molecules between the gas and condensed phases may be confined to the surface region when RH ≤ 30%, suggesting the importance of an adsorption-type mechanism for partitioning in this regime. By comparison, for RH ≥ 70% partitioning of organic molecules may effectively occur by an absorption mechanism throughout the bulk of the particle. Finally, the net uptake rates of semi-reactive atmospheric oxidants such as O3 are expected to decrease by two to five orders of magnitude for a change in RH from 90% to ≤ 30% RH, with possible implications for the rates of chemical aging of SOM particles in the atmosphere.

  6. Viscosity of α-pinene secondary organic material and implications for particle growth and reactivity

    PubMed Central

    Renbaum-Wolff, Lindsay; Grayson, James W.; Bateman, Adam P.; Kuwata, Mikinori; Sellier, Mathieu; Murray, Benjamin J.; Shilling, John E.; Martin, Scot T.; Bertram, Allan K.

    2013-01-01

    Particles composed of secondary organic material (SOM) are abundant in the lower troposphere. The viscosity of these particles is a fundamental property that is presently poorly quantified yet required for accurate modeling of their formation, growth, evaporation, and environmental impacts. Using two unique techniques, namely a “bead-mobility” technique and a “poke-flow” technique, in conjunction with simulations of fluid flow, the viscosity of the water-soluble component of SOM produced by α-pinene ozonolysis is quantified for 20- to 50-μm particles at 293–295 K. The viscosity is comparable to that of honey at 90% relative humidity (RH), similar to that of peanut butter at 70% RH, and at least as viscous as bitumen at ≤30% RH, implying that the studied SOM ranges from liquid to semisolid or solid across the range of atmospheric RH. These data combined with simple calculations or previous modeling studies are used to show the following: (i) the growth of SOM by the exchange of organic molecules between gas and particle may be confined to the surface region of the particles for RH ≤ 30%; (ii) at ≤30% RH, the particle-mass concentrations of semivolatile and low-volatility organic compounds may be overpredicted by an order of magnitude if instantaneous equilibrium partitioning is assumed in the bulk of SOM particles; and (iii) the diffusivity of semireactive atmospheric oxidants such as ozone may decrease by two to five orders of magnitude for a drop in RH from 90% to 30%. These findings have possible consequences for predictions of air quality, visibility, and climate. PMID:23620520

  7. The influence of semi-volatile and reactive primary emissions on the abundance and properties of global organic aerosol

    NASA Astrophysics Data System (ADS)

    Jathar, S. H.; Farina, S. C.; Robinson, A. L.; Adams, P. J.

    2012-04-01

    Semi-volatile and reactive primary organic aerosols are modeled on a global scale using the GISS GCM II' "unified" climate model. We employ the volatility basis set framework to simulate emissions, chemical reactions and phase partitioning of primary and secondary organic aerosol (POA and SOA). The model also incorporates the emissions and reactions of intermediate volatility organic compounds (IVOCs) as a source of organic aerosol (OA), one that has been missing in most prior work. Model predictions are evaluated against a broad set of observational constraints including mass concentrations, degree of oxygenation, volatility and isotopic composition. A traditional model that treats POA as non-volatile and non-reactive is also compared to the same set of observations to highlight the progress made in this effort. The revised model predicts a global dominance of SOA and brings the POA/SOA split into better agreement with ambient measurements. This change is due to traditionally defined POA evaporating and the evaporated vapors oxidizing to form non-traditional SOA. IVOCs (traditionally not included in chemical transport models) oxidize to form condensable products that account for a third of total OA, suggesting that global models have been missing a large source of OA. Predictions of the revised model for the SOA fraction at 17 different locations compared much better to observations than predictions from the traditional model. Model-predicted volatility is compared with thermodenuder data collected at three different field campaigns: FAME-2008, MILAGRO-2006 and SOAR-2005. The revised model predicts the OA volatility much more closely than the traditional model. When compared against monthly averaged OA mass concentrations measured by the IMPROVE network, predictions of both the revised and traditional model lie within a factor of two in summer and mostly within a factor of five during winter. A sensitivity analysis indicates that the winter comparison can be

  8. Interstellar/Precometary Organic Material and the Photochemical Evolution of Complex Organics

    NASA Technical Reports Server (NTRS)

    Allamandola, Lou J.; Bernstein, Max; Sandford, Scott; Witteborn, Fred (Technical Monitor)

    1996-01-01

    During the past two decades ground-, air-, and space-based infrared spectroscopic observations, combined with realistic laboratory simulations, have revolutionized our understanding of interstellar ice and dust, the raw materials from which planets, comets and stars form. Most interstellar material is concentrated in Large molecular clouds where simple molecules are formed by dust grain and gas phase reactions. Gaseous species striking the cold (10 K) dust will stick, forming an icy grain mantle. This accretion, coupled with energetic particle bombardment and UV photolysis, will produce a complex chemical mixture containing volatile, non-volatile, and isotopically fractionated species. Ices in molecular clouds contain the very simple molecules H2O, CH3OH, CO, CO2, H2, and perhaps some NH3 and H2CO, as well as more complex species including nitriles and ketones or esters. The evidence for these compounds as well as carbon rich materials such as polycyclic aromatic hydrocarbons (PAHs), microdiamonds, and amorphous carbon will be reviewed and the possible connections with comets and meteorites will be presented in the first part of the talk. The second part of the presentation will focus on interstellar/precometary ice photochemical evolution. The chemical composition and photochemical evolution of realistic interstellar/pre-cometary ice analogs containing methanol will be discussed. ultraviolet photolysis of these ices produces H2, H2CO, CO2, CO, CH4, HCO, and more complex molecules. Infrared spectroscopy, H-1 and C-13 nuclear magnetic resonance (NMR) spectroscopy, and gas chromatography-mass spectrometry demonstrate that when ices representative of interstellar grains and comets are exposed to UV radiation at low temperature a series of moderately complex organic molecules are formed in the ice including: CH3CH2OH (ethanol), HC(=O)NH2 (formamide), CH3C(=O)NH2 (acetamide), and R-C(integral)N (nitriles). Several of these are already known to be in the interstellar

  9. High liquid yield process for retorting various organic materials including oil shale

    DOEpatents

    Coburn, Thomas T.

    1990-01-01

    This invention is a continuous retorting process for various high molecular weight organic materials, including oil shale, that yields an enhanced output of liquid product. The organic material, mineral matter, and an acidic catalyst, that appreciably adsorbs alkenes on surface sites at prescribed temperatures, are mixed and introduced into a pyrolyzer. A circulating stream of olefin enriched pyrolysis gas is continuously swept through the organic material and catalyst, whereupon, as the result of pyrolysis, the enhanced liquid product output is provided. Mixed spent organic material, mineral matter, and cool catalyst are continuously withdrawn from the pyrolyzer. Combustion of the spent organic material and mineral matter serves to reheat the catalyst. Olefin depleted pyrolysis gas, from the pyrolyzer, is enriched in olefins and recycled into the pyrolyzer. The reheated acidic catalyst is separated from the mineral matter and again mixed with fresh organic material, to maintain the continuously cyclic process.

  10. A high liquid yield process for retorting various organic materials including oil shale

    DOEpatents

    Coburn, T.T.

    1988-07-26

    This invention is a continuous retorting process for various high molecular weight organic materials, including oil shale, that yields an enhanced output of liquid product. The organic material, mineral matter, and an acidic catalyst, that appreciably adsorbs alkenes on surface sites at prescribed temperatures, are mixed and introduced into a pyrolyzer. A circulating stream of olefin enriched pyrolysis gas is continuously swept through the organic material and catalyst, whereupon, as the result of pyrolysis, the enhanced liquid product output is provided. Mixed spent organic material, mineral matter, and cool catalyst are continuously withdrawn from the pyrolyzer. Combustion of the spent organic material and mineral matter serves to reheat the catalyst. Olefin depleted pyrolysis gas, from the pyrolyzer, is enriched in olefins and recycled into the pyrolyzer. The reheated acidic catalyst is separated from the mineral matter and again mixed with fresh organic material, to maintain the continuously cyclic process. 2 figs.

  11. Effect of petroleum products on the decomposition of soil organic matter as assessed by 13C natural abundance

    NASA Astrophysics Data System (ADS)

    Stelmach, Wioleta; Szarlip, Paweł; Trembaczowski, Andrzej; Bieganowski, Andrzej

    2016-04-01

    Petroleum products are common contaminants in soils due to human activities. They are toxic for microorganisms and threat their functions, including decomposition of soil organic matter (SOM). The direct estimation of altered SOM decomposition - based on the CO2 emission - is impossible after oil contamination, because oil decomposition also contributes to the CO2 release. We used the natural differences in the isotopic signature (δ13C) of SOM and of oil products to partition the total CO2 for both sources and to analyze the suppression of SOM decomposition. The dynamics of 13C fractionation during the mineralization of gasoline and diesel was measured during 42 days. The 13C fractionation varied between -8.8‰ and +3.6‰ within the first 10 days, and stabilized thereafter at about -5.3‰ for gasoline and +3.2‰ for diesel. These 13C fractionations and δ13C values of CO2 emitted from the soil were used for correct partitioning of the total CO2. Contamination with gasoline reduced the CO2 efflux from SOM decomposition by a factor of 25 (from 151 to 6 mg C-CO2 kg‑1 soil during 42 days). The negative effect of diesel was much lower: the CO2 efflux from SOM was decreased by less than a factor of 2. The strong effect of gasoline versus diesel reflects the lower absorption of gasoline to mineral particles and the development of a thin film on water surfaces, leading to toxicity for microorganisms. We conclude that the small differences of 13C of SOM and of organic pollutants can be used to partition CO2 fluxes and analyze pollutant effects on SOM decomposition.

  12. Structured organic materials and devices using low-energy particle beams

    DOEpatents

    Vardeny, Z. Valy; Li, Sergey; Delong, Matthew C.; Jiang, Xiaomei

    2005-09-13

    Organic materials exposed to an electron beam for patterning a substrate (1) to make an optoelectronic organic device which includes a source, a drain, gate dielectric layer (4), and a substrate for emitting light.

  13. Synthesis of Linearly Fused Benzodipyrrole Based Organic Materials.

    PubMed

    Vlasselaer, Maarten; Dehaen, Wim

    2016-01-01

    The objective of this review is to give an overview of the synthetic methods to prepare different indolo[3,2-b]carbazoles and similar systems with a potential use in electro-optical devices such as OLEDs (organic light emitting diode), OPVs (organic photovoltaic) and OFETs (organic field effect transistor). Some further modifications to the core units and their implications for specific applications are also discussed. PMID:27322228

  14. Model-measurement comparison of functional group abundance in α-pinene and 1,3,5-trimethylbenzene secondary organic aerosol formation

    NASA Astrophysics Data System (ADS)

    Ruggeri, Giulia; Bernhard, Fabian A.; Henderson, Barron H.; Takahama, Satoshi

    2016-07-01

    Secondary organic aerosol (SOA) formed by α-pinene and 1,3,5-trimethylbenzene photooxidation under different NOx regimes is simulated using the Master Chemical Mechanism v3.2 (MCM) coupled with an absorptive gas-particle partitioning module. Vapor pressures for individual compounds are estimated with the SIMPOL.1 group contribution model for determining apportionment of reaction products to each phase. We apply chemoinformatic tools to harvest functional group (FG) composition from the simulations and estimate their contributions to the overall oxygen to carbon ratio. Furthermore, we compare FG abundances in simulated SOA to measurements of FGs reported in previous chamber studies using Fourier transform infrared spectroscopy. These simulations qualitatively capture the dynamics of FG composition of SOA formed from both α-pinene and 1,3,5-trimethylbenzene in low-NOx conditions, especially in the first hours after start of photooxidation. Higher discrepancies are found after several hours of simulation; the nature of these discrepancies indicates sources of uncertainty or types of reactions in the condensed or gas phase missing from current model implementation. Higher discrepancies are found in the case of α-pinene photooxidation under different NOx concentration regimes, which are reasoned through the domination by a few polyfunctional compounds that disproportionately impact the simulated FG abundance in the aerosol phase. This manuscript illustrates the usefulness of FG analysis to complement existing methods for model-measurement evaluation.

  15. A porous proton-relaying metal-organic framework material that accelerates electrochemical hydrogen evolution.

    PubMed

    Hod, Idan; Deria, Pravas; Bury, Wojciech; Mondloch, Joseph E; Kung, Chung-Wei; So, Monica; Sampson, Matthew D; Peters, Aaron W; Kubiak, Cliff P; Farha, Omar K; Hupp, Joseph T

    2015-01-01

    The availability of efficient hydrogen evolution reaction (HER) catalysts is of high importance for solar fuel technologies aimed at reducing future carbon emissions. Even though Pt electrodes are excellent HER electrocatalysts, commercialization of large-scale hydrogen production technology requires finding an equally efficient, low-cost, earth-abundant alternative. Here, high porosity, metal-organic framework (MOF) films have been used as scaffolds for the deposition of a Ni-S electrocatalyst. Compared with an MOF-free Ni-S, the resulting hybrid materials exhibit significantly enhanced performance for HER from aqueous acid, decreasing the kinetic overpotential by more than 200 mV at a benchmark current density of 10 mA cm(-2). Although the initial aim was to improve electrocatalytic activity by greatly boosting the active area of the Ni-S catalyst, the performance enhancements instead were found to arise primarily from the ability of the proton-conductive MOF to favourably modify the immediate chemical environment of the sulfide-based catalyst. PMID:26365764

  16. A porous proton-relaying metal-organic framework material that accelerates electrochemical hydrogen evolution

    SciTech Connect

    Hod, Idan; Deria, Pravas; Bury, Wojciech; Mondloch, Joseph E.; Kung, Chung-Wei; So, Monica; Sampson, Matthew D.; Peters, Aaron W.; Kubiak, Cliff P.; Farha, Omar K.; Hupp, Joseph T.

    2015-09-14

    The availability of efficient hydrogen evolution reaction (HER) catalysts is of high importance for solar fuel technologies aimed at reducing future carbon emissions. Even though Pt electrodes are excellent HER electrocatalysts, commercialization of large-scale hydrogen production technology requires finding an equally efficient, low-cost, earth-abundant alternative. Here, high porosity, metal-organic framework (MOF) films have been used as scaffolds for the deposition of a Ni-S electrocatalyst. Compared with an MOF-free Ni-S, the resulting hybrid materials exhibit significantly enhanced performance for HER from aqueous acid, decreasing the kinetic overpotential by more than 200 mV at a benchmark current density of 10 mA cm−2. In conclusion, although the initial aim was to improve electrocatalytic activity by greatly boosting the active area of the Ni-S catalyst, the performance enhancements instead were found to arise primarily from the ability of the proton-conductive MOF to favourably modify the immediate chemical environment of the sulfide-based catalyst.

  17. A porous proton-relaying metal-organic framework material that accelerates electrochemical hydrogen evolution

    DOE PAGESBeta

    Hod, Idan; Deria, Pravas; Bury, Wojciech; Mondloch, Joseph E.; Kung, Chung-Wei; So, Monica; Sampson, Matthew D.; Peters, Aaron W.; Kubiak, Cliff P.; Farha, Omar K.; et al

    2015-09-14

    The availability of efficient hydrogen evolution reaction (HER) catalysts is of high importance for solar fuel technologies aimed at reducing future carbon emissions. Even though Pt electrodes are excellent HER electrocatalysts, commercialization of large-scale hydrogen production technology requires finding an equally efficient, low-cost, earth-abundant alternative. Here, high porosity, metal-organic framework (MOF) films have been used as scaffolds for the deposition of a Ni-S electrocatalyst. Compared with an MOF-free Ni-S, the resulting hybrid materials exhibit significantly enhanced performance for HER from aqueous acid, decreasing the kinetic overpotential by more than 200 mV at a benchmark current density of 10 mA cm−2. In conclusion, althoughmore » the initial aim was to improve electrocatalytic activity by greatly boosting the active area of the Ni-S catalyst, the performance enhancements instead were found to arise primarily from the ability of the proton-conductive MOF to favourably modify the immediate chemical environment of the sulfide-based catalyst.« less

  18. A porous proton-relaying metal-organic framework material that accelerates electrochemical hydrogen evolution

    NASA Astrophysics Data System (ADS)

    Hod, Idan; Deria, Pravas; Bury, Wojciech; Mondloch, Joseph E.; Kung, Chung-Wei; So, Monica; Sampson, Matthew D.; Peters, Aaron W.; Kubiak, Cliff P.; Farha, Omar K.; Hupp, Joseph T.

    2015-09-01

    The availability of efficient hydrogen evolution reaction (HER) catalysts is of high importance for solar fuel technologies aimed at reducing future carbon emissions. Even though Pt electrodes are excellent HER electrocatalysts, commercialization of large-scale hydrogen production technology requires finding an equally efficient, low-cost, earth-abundant alternative. Here, high porosity, metal-organic framework (MOF) films have been used as scaffolds for the deposition of a Ni-S electrocatalyst. Compared with an MOF-free Ni-S, the resulting hybrid materials exhibit significantly enhanced performance for HER from aqueous acid, decreasing the kinetic overpotential by more than 200 mV at a benchmark current density of 10 mA cm-2. Although the initial aim was to improve electrocatalytic activity by greatly boosting the active area of the Ni-S catalyst, the performance enhancements instead were found to arise primarily from the ability of the proton-conductive MOF to favourably modify the immediate chemical environment of the sulfide-based catalyst.

  19. A porous proton-relaying metal-organic framework material that accelerates electrochemical hydrogen evolution

    PubMed Central

    Hod, Idan; Deria, Pravas; Bury, Wojciech; Mondloch, Joseph E.; Kung, Chung-Wei; So, Monica; Sampson, Matthew D.; Peters, Aaron W.; Kubiak, Cliff P.; Farha, Omar K.; Hupp, Joseph T.

    2015-01-01

    The availability of efficient hydrogen evolution reaction (HER) catalysts is of high importance for solar fuel technologies aimed at reducing future carbon emissions. Even though Pt electrodes are excellent HER electrocatalysts, commercialization of large-scale hydrogen production technology requires finding an equally efficient, low-cost, earth-abundant alternative. Here, high porosity, metal-organic framework (MOF) films have been used as scaffolds for the deposition of a Ni-S electrocatalyst. Compared with an MOF-free Ni-S, the resulting hybrid materials exhibit significantly enhanced performance for HER from aqueous acid, decreasing the kinetic overpotential by more than 200 mV at a benchmark current density of 10 mA cm−2. Although the initial aim was to improve electrocatalytic activity by greatly boosting the active area of the Ni-S catalyst, the performance enhancements instead were found to arise primarily from the ability of the proton-conductive MOF to favourably modify the immediate chemical environment of the sulfide-based catalyst. PMID:26365764

  20. High-precision optical measurements of 13C/12C isotope ratios in organic compounds at natural abundance

    PubMed Central

    Zare, Richard N.; Kuramoto, Douglas S.; Haase, Christa; Tan, Sze M.; Crosson, Eric R.; Saad, Nabil M. R.

    2009-01-01

    A continuous-flow cavity ring-down spectroscopy (CRDS) system integrating a chromatographic separation technique, a catalytic combustor, and an isotopic 13C/12C optical analyzer is described for the isotopic analysis of a mixture of organic compounds. A demonstration of its potential is made for the geochemically important class of short-chain hydrocarbons. The system proved to be linear over a 3-fold injection volume dynamic range with an average precision of 0.95‰ and 0.67‰ for ethane and propane, respectively. The calibrated accuracy for methane, ethane, and propane is within 3‰ of the values determined using isotope ratio mass spectrometry (IRMS), which is the current method of choice for compound-specific isotope analysis. With anticipated improvements, the low-cost, portable, and easy-to-use CRDS-based instrumental setup is poised to evolve into a credible challenge to the high-cost and complex IRMS-based technique. PMID:19564619

  1. Ultrafast Spectroscopy in Conjugated Organic and Biological Materials

    NASA Astrophysics Data System (ADS)

    Yan, Ming

    The dynamics of two kinds of conjugated materials, the visual pigment rhodopsin and the organic polymer poly(p -phenylene vinylene), have been studied utilizing femtosecond spectroscopy. The 11-cis to all-trans torsional isomerization of the retinal chromophore in rhodopsin for both protonated and deuterated aqueous environments have been studied by time-resolved absorption measurements at room temperature. The kinetic results are well modeled by rate equations based on the scheme which involves the isomerization along the torsional coordinate of the 11-cis bond of the retinal chromophore. A metastable intermediate 90 degree twisted state is formed within 200 fs on the excited state surface by rotation around the C_{11} -C_{12} double bond, and it takes 3 ps to form the fully isomerized all -trans photoproduct known as bathorhodopsin and to repopulate the ground state rhodopsin. These results agree well with the semiempirical energy level and molecular dynamics calculations. The observed dynamics are insensitive to deuteration of the exchangeable protons which suggest that proton translocation is unimportant at physiological temperatures. The conjugated polymer, Poly(p-phenylene vinylene) (PPV) in a stretch oriented film, has been studied using polarized time-resolved absorption with subpicosecond resolution and transient luminescence measurements. Excitations are generated by photoexcitation near the band edge (500nm -540nm) with a 200 fs pulse and the resulting spectral changes are probed with a white light pulse. Lattice stabilized (singlet) self-trapped excitons are formed within 200 fs which are observed by measuring the stimulated gain in their emission band which decay at 10 ps. The agreement of the photoinduced exciton gain spectrum (<1ps), the transient luminescence spectrum (10 ps) and the steady state luminescence spectrum suggest that the singlet excitons are not further trapped after 200fs of their formation time. Excitation wavelength dependence

  2. ADSORPTION OF ORGANIC CATIONS TO SOILS AND SUBSURFACE MATERIALS

    EPA Science Inventory

    A study of the fundamentals of adsorption of amphiphilic organic cations on natural and pristine surfaces was conducted to elucidate (i) the factors that influence the extent of adsorption and (ii) indirect effects of adsorption of organic cations: the competitive adsorption of o...

  3. Small organic solutes in sticky droplets from orb webs of the spider Zygiella atrica (Araneae; Araneidae): β-alaninamide is a novel and abundant component.

    PubMed

    Townley, Mark A; Pu, Qinglin; Zercher, Charles K; Neefus, Christopher D; Tillinghast, Edward K

    2012-10-01

    In northeastern North America, Zygiella atrica often build their orb webs near the ocean. We analyzed individual field-built Z. atrica webs to determine if organic low-molecular-mass solutes (LMM) in their sticky droplets showed any unusual features not previously seen in orb webs of other species living in less salty environments. While two of the three most abundant organic LMM (putrescine (butane-1,4-diamine) and GABamide (4-aminobutanamide)) are already well-known from webs of inland spiders, the third major LMM, β-alaninamide (3-aminopropanamide), a homolog of GABamide, has not been detected in sticky droplets from any other araneoid spiders (27 species). It remains to be established, however, whether or not use of β-alaninamide is related to proximity to saltwater. We observed variability in organic LMM composition in Z. atrica webs that appeared to be influenced more by an undetermined factor associated with different collecting locations and/or collection dates than by different genders or instars. Shifts in composition when adult females were transferred from the field to the laboratory were also observed. Structural similarities and inverse correlations among β-alaninamide, GABamide, and N-acetylputrescine suggest that they may form a series of LMM fulfilling essentially the same, as yet unknown, role in the webs of those species in which they occur. PMID:23081916

  4. Ionic and electronic behaviors of earth-abundant semiconductor materials and their applications toward solar energy harvesting

    NASA Astrophysics Data System (ADS)

    Mayer, Matthew T.

    Semiconductor devices offer promise for efficient conversion of sunlight into other useful forms of energy, in either photovoltaic or photoelectrochemical cell configurations to produce electrical power or chemical energy, respectively. This dissertation examines ionic and electronic phenomena in some candidate semiconductors and seeks to understand their implications toward solar energy conversion applications. First, copper sulfide (Cu2S) was examined as a candidate photovoltaic material. It was discovered that its unique property of cation diffusion allows the room-temperature synthesis of vertically-aligned nanowire arrays, a morphology which facilitates study of the diffusion processes. This diffusivity was found to induce hysteresis in the electronic behavior, leading to the phenomena of resistive switching and negative differential resistance. The Cu2S were then demonstrated as morphological templates for solid-state conversion into different types of heterostructures, including segmented and rod-in-tube morphologies. Near-complete conversion to ZnS, enabled by the out-diffusion of Cu back into the substrate, was also achieved. While the ion diffusion property likely hinders the reliability of Cu 2S in photovoltaic applications, it was shown to enable useful electronic and ionic behaviors. Secondly, iron oxide (Fe2O3, hematite) was examined as a photoanode for photoelectrochemical water splitting. Its energetic limitations toward the water electrolysis reactions were addressed using two approaches aimed at achieving greater photovoltages and thereby improved water splitting efficiencies. In the first, a built-in n-p junction produced an internal field to drive charge separation and generate photovoltage. In the second, Fe 2O3 was deposited onto a smaller band gap material, silicon, to form a device capable of producing enhanced total photovoltage by a dual-absorber Z-scheme mechanism. Both approaches resulted in a cathodic shift of the photocurrent onset

  5. MEASUREMENT OF POLYCYCLIC ORGANIC MATERIALS AND OTHER HAZARDOUS ORGANIC COMPOUNDS IN STACK GASES - STATE OF THE ART

    EPA Science Inventory

    This report documents and reviews state-of-the-art methods for the measurement of polycyclic organic matter (POM) and other hazardous organic materials which are present in industrial stack emissions. Measurement methods for many hazardous compounds, such as POM and nitrosamines,...

  6. Growth of bulk single crystals of organic materials for nonlinear optical devices - An overview

    NASA Technical Reports Server (NTRS)

    Penn, Benjamin G.; Cardelino, Beatriz H.; Moore, Craig E.; Shields, Angela W.; Frazier, D. O.

    1991-01-01

    Highly perfect single crystals of nonlinear optical organic materials are required for use in optical devices. An overview of the bulk crystal growth of these materials by melt, vapor, and solution processes is presented. Additionally, methods that may be used to purify starting materials, detect impurities at low levels, screen materials for crystal growth, and process grown crystals are discussed.

  7. Biomimetic synthesis of shaped and chiral silica entities templated by organic objective materials.

    PubMed

    Jin, Ren-Hua; Yao, Dong-Dong; Levi, Rumi Tamoto

    2014-06-10

    Organic molecules with accompanying self-organization have been a great subject in chemistry, material science and nanotechnology in the past two decades. One of the most important roles of organized organic molecules is the capability of templating complexly structured inorganic materials. The focus of this Minireview is on nanostructured silica with divergent morphologies and/or integrated chirality directed by organic templates of self-assembled polyamine/polypeptides/block copolymers, chiral organogels, self-organized chiral amphiphiles and chiral crystalline complexes, etc., by biomimetic silicification and conventional sol-gel reaction. Among them, biosilica (diatoms and sponges)-inspired biomimetic silicifications are particularly highlighted. PMID:24861362

  8. Influence of pregnancy in mid-to-late gestation on circulating metabolites, visceral organ mass, and abundance of proteins relating to energy metabolism in mature beef cows.

    PubMed

    Wood, K M; Awda, B J; Fitzsimmons, C; Miller, S P; McBride, B W; Swanson, K C

    2013-12-01

    In mid-to-late gestation, nutrient demand increases to meet the growth requirements of the conceptus and cows may alter metabolism in response to energy demands of pregnancy. By better understanding the metabolic role of pregnancy, there may be opportunities to better understand maintenance energy costs and improve overall feed efficiency. Eighteen mature Simmental/Angus crossbred cows, pregnant (PREG; n = 9) and nonpregnant (OPEN; n = 9), were used to investigate the effect of pregnancy on BW change, carcass traits, visceral organ mass, and circulating serum metabolites. Cows were blocked by day of expected parturition such that each block was slaughtered 4 to 5 wk before parturition. Cows were individually fed for ad libitum intake using Calan gates for 89 to 105 d. Cows were weighed, ultrasounded for rib (over the 12th and 13th rib) and rump fat, and a serum sample obtained at d 1, 56, and 3 to 5 d before slaughter. At slaughter, organs were removed, trimmed of fat, and weighed. Serum was analyzed for β-hydroxybutyrate (BHBA), NEFA, glucose, urea, total cholesterol, and triiodothyronine (T3). Tissue samples from liver, kidney, sternomandibularis muscle, ruminal papillae, pancreas, and small intestinal mucosa were collected at slaughter and snap frozen in liquid N. Western blots were conducted to quantify abundance of: proliferating cell nuclear antigen (PCNA), ATP synthase, ubiquitin, and Na(+)/K+ ATPase for all tissues; PPARγ, PPARγ coactivator 1α (PGC1-α), 5'-adenosine monophosphate-activated protein kinase (AMPK) and phosphorylated-AMPK (pAMPK) for liver, muscle, and rumen; phosphoenolpyruvate carboxykinase (PEPCK) for liver and kidney; and uncoupling protein 2 (UCP2) for liver. Data were analyzed using PROC MIXED in SAS as a replicated randomized complete block. Liver weights (actual, relative to BW, relative to HCW) were heavier (P ≤ 0.02) in OPEN. Rumen mass and kidney fat weight, both relative to BW, were also greater (P ≤ 0.04) in OPEN. On d 56

  9. The Purification, Properties, and Localization of an Abundant Legume Seed Lectin Cross-Reactive Material from Spartium junceum 1

    PubMed Central

    Hankins, Charles N.; Herman, Eliot M.; Kindinger, Juanita; Shannon, Leland M.

    1991-01-01

    The seeds of Spartium junceum contained a large quantity of lectin-like protein that did not appear to be either a hemagglutinin or active lectin. The cross-reactive material (CRM), like most legume seed lectins, was a tetrameric glycoprotein of about 130,000 Mr. The singlesized subunits of about 33,000 Mr were not covalently associated. The amino acid composition was typical of legume lectins and was rich in hydroxy-amino acids and poor in sulfur-containing amino acids. The Spartium CRM contained about 3.5% covalently associated carbohydrate, most likely of the high-mannose type, since the CRM was precipitated by concanavalin A. The CRM was localized by electron-microscopic immunocytochemistry and found to be exclusively in protein-filled vacuoles (protein bodies). Because this protein was so similar immunologically, structurally, and in its physiology, to classic legume seed lectins, it is most likely a lectin homolog. Similar seed lectin CRMs appear to be both common and widespread in the Leguminosae. ImagesFigure 1Figure 2Figure 3Figure 4 PMID:16668191

  10. U, Th, Pb and REE abundances and Pb 207/Pb 206 ages of individual minerals in returned lunar material by ion microprobe mass analysis.

    NASA Technical Reports Server (NTRS)

    Andersen, C. A.; Hinthorne, J. R.

    1972-01-01

    Results of ion microprobe analyses of Apollo 11, 12 and 14 material, showing that U, Th, Pb and REE are concentrated in accessory minerals such as apatite, whitlockite, zircon, baddeleyite, zirkelite, and tranquillityite. Th/U ratios are found to vary by over a factor of 40 in these minerals. K, Ba, Rb and Sr have been localized in a K rich, U and Th poor glass phase that is commonly associated with the U and Th bearing accessory minerals. Li is observed to be fairly evenly distributed between the various accessory phases. The phosphates have been found to have REE abundance patterns (normalized to the chondrite abundances) that are fairly flat, while the Zr bearing minerals have patterns that rise steeply, by factors of ten or more, from La to Gd. All the accessory minerals have large negative Eu anomalies. Radiometric age dates (Pb 207/Pb 206) of the individual U and Th bearing minerals compare favorably with the Pb 207/Pb 206 age of the bulk rocks.

  11. The Suzaku Observation of the Nucleus of the Radio Loud Active Galaxy Centaurus A: Constraints on Abundances in the Accreting Material

    NASA Technical Reports Server (NTRS)

    Markowitz, A.; Takahashi, T.A; Watanabe, S.; Nakazawa, K.; Fukazawa, Y.; Kokubun, M.; Makishima, K.; Awaki, H.; Bamba, A.; Isobe, N.; Kataoka, J.; Madejski, G.; Mushotzky, R.; Okajima, T.; Ptak, A.; Reeves, J. N.; Ueda, Y.; Yamasaki, T.; Yaqoob, T.

    2007-01-01

    A Suzaku observation of the nucleus of the radio-loud AGN Centaurus A in 2005 has yielded a broadband spectrum spanning 0.3 to 250 keV. The hard X-rays are fit by two power laws, absorbed by columns of 1.5 and 7 x 10(exp 23) per square centimeter. The dual power-laws are consistent with previous suggestions that the powerlaw components are X-ray emission from the sub-pc VLBI jet and from Bondi accretion at the core, or are consistent with a partial covering interpretation. The soft band is dominated by thermal emission from the diffuse plasma and is fit well by a two-temperature VAPEC model, plus a third power-law component to account for scattered nuclear emission, kpc-scale jet emission, and emission from X-ray Binaries and other point sources. Narrow fluorescent emission lines from Fe, Si, S, Ar, Ca and Ni are detected. The width of the Fe Ka line yields a 200 light-day lower limit on the distance from the black hole to the line-emitting gas. K-shell absorption edges due to Fe, Ca, and S are detected. Elemental abundances are constrained via the fluorescent lines strengths, absorption edge depths and the diffuse plasma emission lines. The high metallicity ([Fe/H]=+0.l) of the circumnuclear material compared to that in the metal-poor outer halo suggests that the accreting material could not have originated in the outer halo unless enrichment by local star formation has occurred. Relative abundances are consistent with enrichment from Type II and Ia supernovae.

  12. Integrated Charge Transfer in Organic Ferroelectrics for Flexible Multisensing Materials.

    PubMed

    Xu, Beibei; Ren, Shenqiang

    2016-09-01

    The ultimate or end point of functional materials development is the realization of strong coupling between all energy regimes (optical, electronic, magnetic, and elastic), enabling the same material to be utilized for multifunctionalities. However, the integration of multifunctionalities in soft materials with the existence of various coupling is still in its early stage. Here, the coupling between ferroelectricity and charge transfer by combining bis(ethylenedithio)tetrathiafulvalene-C60 charge-transfer crystals with ferroelectric polyvinylidene fluoride polymer matrix is reported, which enables external stimuli-controlled polarization, optoelectronic and magnetic field sensing properties. Such flexible composite films also display a superior strain-dependent capacitance and resistance change with a giant piezoresistance coefficient of 7.89 × 10(-6) Pa(-1) . This mutual coupled material with the realization of enhanced couplings across these energy domains opens up the potential for multisensing applications. PMID:27378088

  13. Selective Bifunctional Modification of a Non-catenated Metal-Organic Framework Material via 'Click' Chemistry

    SciTech Connect

    Gadzikwa, Tendai; Farha, Omar K.; Malliakas, Christos D.; Kanatzidis, Mercouri G.; Hupp, Joseph T.; Nguyen, SonBinh T.; NWU

    2009-12-01

    A noncatenated, Zn-based metal-organic framework (MOF) material bearing silyl-protected acetylenes was constructed and postsynthetically modified using 'click' chemistry. Using a solvent-based, selective deprotection strategy, two different organic azides were 'clicked' onto the MOF crystals, resulting in a porous material whose internal and external surfaces are differently functionalized.

  14. Nicotine, acetanilide and urea multi-level2H-,13C- and15N-abundance reference materials for continuous-flow isotope ratio mass spectrometry

    USGS Publications Warehouse

    Schimmelmann, A.; Albertino, A.; Sauer, P.E.; Qi, H.; Molinie, R.; Mesnard, F.

    2009-01-01

    Accurate determinations of stable isotope ratios require a calibration using at least two reference materials with different isotopic compositions to anchor the isotopic scale and compensate for differences in machine slope. Ideally, the S values of these reference materials should bracket the isotopic range of samples with unknown S values. While the practice of analyzing two isotopically distinct reference materials is common for water (VSMOW-SLAP) and carbonates (NBS 19 and L-SVEC), the lack of widely available organic reference materials with distinct isotopic composition has hindered the practice when analyzing organic materials by elemental analysis/isotope ratio mass spectrometry (EA-IRMS). At present only L-glutamic acids USGS40 and USGS41 satisfy these requirements for ??13C and ??13N, with the limitation that L-glutamic acid is not suitable for analysis by gas chromatography (GC). We describe the development and quality testing of (i) four nicotine laboratory reference materials for on-line (i.e. continuous flow) hydrogen reductive gas chromatography-isotope ratio mass-spectrometry (GC-IRMS), (ii) five nicotines for oxidative C, N gas chromatography-combustion-isotope ratio mass-spectrometry (GC-C-IRMS, or GC-IRMS), and (iii) also three acetanilide and three urea reference materials for on-line oxidative EA-IRMS for C and N. Isotopic off-line calibration against international stable isotope measurement standards at Indiana University adhered to the 'principle of identical treatment'. The new reference materials cover the following isotopic ranges: ??2Hnicotine -162 to -45%o, ??13Cnicotine -30.05 to +7.72%, ?? 15Nnicotine -6.03 to +33.62%; ??15N acetanilide +1-18 to +40.57%; ??13Curea -34.13 to +11.71%, ??15Nurea +0.26 to +40.61% (recommended ?? values refer to calibration with NBS 19, L-SVEC, IAEA-N-1, and IAEA-N-2). Nicotines fill a gap as the first organic nitrogen stable isotope reference materials for GC-IRMS that are available with different ??13N

  15. Nicotine, acetanilide and urea multi-level 2H-, 13C- and 15N-abundance reference materials for continuous-flow isotope ratio mass spectrometry.

    PubMed

    Schimmelmann, Arndt; Albertino, Andrea; Sauer, Peter E; Qi, Haiping; Molinie, Roland; Mesnard, François

    2009-11-01

    Accurate determinations of stable isotope ratios require a calibration using at least two reference materials with different isotopic compositions to anchor the isotopic scale and compensate for differences in machine slope. Ideally, the delta values of these reference materials should bracket the isotopic range of samples with unknown delta values. While the practice of analyzing two isotopically distinct reference materials is common for water (VSMOW-SLAP) and carbonates (NBS 19 and L-SVEC), the lack of widely available organic reference materials with distinct isotopic composition has hindered the practice when analyzing organic materials by elemental analysis/isotope ratio mass spectrometry (EA-IRMS). At present only L-glutamic acids USGS40 and USGS41 satisfy these requirements for delta13C and delta15N, with the limitation that L-glutamic acid is not suitable for analysis by gas chromatography (GC). We describe the development and quality testing of (i) four nicotine laboratory reference materials for on-line (i.e. continuous flow) hydrogen reductive gas chromatography-isotope ratio mass-spectrometry (GC-IRMS), (ii) five nicotines for oxidative C, N gas chromatography-combustion-isotope ratio mass-spectrometry (GC-C-IRMS, or GC-IRMS), and (iii) also three acetanilide and three urea reference materials for on-line oxidative EA-IRMS for C and N. Isotopic off-line calibration against international stable isotope measurement standards at Indiana University adhered to the 'principle of identical treatment'. The new reference materials cover the following isotopic ranges: delta2H(nicotine) -162 to -45 per thousand, delta13C(nicotine) -30.05 to +7.72 per thousand, delta15N(nicotine) -6.03 to +33.62 per thousand; delta15N(acetanilide) +1.18 to +40.57 per thousand; delta13C(urea) -34.13 to +11.71 per thousand, delta15N(urea) +0.26 to +40.61 per thousand (recommended delta values refer to calibration with NBS 19, L-SVEC, IAEA-N-1, and IAEA-N-2). Nicotines fill a gap as

  16. The origin of charge localization observed in organic photovoltaic materials.

    PubMed

    Johns, James E; Muller, Eric A; Frechet, Jean M J; Harris, Charles B

    2010-11-10

    Two of the primary hurdles facing organic electronics and photovoltaics are their low charge mobility and the inability to disentangle morphological and molecular effects on charge transport. Specific chemical groups such as alkyl side chains are often added to enable spin-casting and to improve overall power efficiency and morphologies, but their exact influence on mobility is poorly understood. Here, we use two-photon photoemission spectroscopy to study the charge transport properties of two organic semiconductors, one with and one without alkyl substituents (sexithiophene and dihexyl-sexithiophene). We show that the hydrocarbon side chains are responsible for charge localization within 230 fs. This implies that other chemical groups should be used instead of alkyl ligands to achieve the highest performance in organic photovoltaics and electronics. PMID:20961096

  17. Advances in phosphors based on organic materials for light emitting devices

    NASA Astrophysics Data System (ADS)

    Sharma, Kashma; Kumar, Vijay; Kumar, Vinod; Swart, Hendrik C.

    2016-01-01

    A brief overview is presented in the light emitting diodes (LEDs) based on purely organic materials. Organic LEDs are of great interest to the research community because of their outstanding properties and flexibility. Comparison between devices made using different organic materials and their derivatives with respect to synthetic protocols, characterizations, quantum efficiencies, sensitivity, specificity and their applications in various fields have been discussed. This review also discusses the essential requirement and scientific issues that arise in synthesizing cost-effective and environmental friendly organic LEDs diodes based on purely organic materials. This mini review aims to capture and convey some of the key current developments in phosphors formed by purely organic materials and highlights some possible future applications. Hence, this study comes up with a widespread discussion on the various contents in a single platform. Also, it offers avenues for new researchers for futuristic development in the area.

  18. Bismuth Interfacial Doping of Organic Small Molecules for High Performance n-type Thermoelectric Materials.

    PubMed

    Huang, Dazhen; Wang, Chao; Zou, Ye; Shen, Xingxing; Zang, Yaping; Shen, Hongguang; Gao, Xike; Yi, Yuanping; Xu, Wei; Di, Chong-An; Zhu, Daoben

    2016-08-26

    Development of chemically doped high performance n-type organic thermoelectric (TE) materials is of vital importance for flexible power generating applications. For the first time, bismuth (Bi) n-type chemical doping of organic semiconductors is described, enabling high performance TE materials. The Bi interfacial doping of thiophene-diketopyrrolopyrrole-based quinoidal (TDPPQ) molecules endows the film with a balanced electrical conductivity of 3.3 S cm(-1) and a Seebeck coefficient of 585 μV K(-1) . The newly developed TE material possesses a maximum power factor of 113 μW m(-1)  K(-2) , which is at the forefront for organic small molecule-based n-type TE materials. These studies reveal that fine-tuning of the heavy metal doping of organic semiconductors opens up a new strategy for exploring high performance organic TE materials. PMID:27496293

  19. High Performance Organic Photovoltaics via Novel Materials Combinations

    SciTech Connect

    Laird, Dr Darin; McGuiness, Dr Christine; Storch, Mark

    2011-01-20

    OPV cell efficiencies have increased significantly over the last decade and verified champion efficiencies are currently at 8.3% for both single and multi-junction device types. These increases in efficiency have been driven through the development and optimization of the donor and acceptor materials in bulk heterojunction active layers. Plextronics and Solarmer Energy Inc. are two of the world leading developers of these donor and acceptor materials. Solarmer Energy has reported NREL certified 6.77% efficiencies using optimized low band gap donor materials in combination with PC61BM and PC71BM acceptors and recently reported a champion NREL certified efficiency of 8.1%. Plextronics has reported Newport certified efficiencies of 6.7% using PC71BM acceptors with low band gap materials. In addition, Plextronics has also demonstrated that OPV efficiency of P3HT based materials can be improved by 50% by improving the Voc using alternative acceptors (indene substituted C60 and C70) to PC61BM and PC71BM. However, performance of these alternative acceptors in combination with low band gap materials has not been investigated and the potential for efficiency improvement is evident. In this collaboration, four low band gap donor materials from Solarmer Energy Inc were combined with Plextronics’ indene-class acceptors Plextronics’ indene substituted C60 and C70 acceptors to demonstrate OPV performance greater than 7%. Two main indene class C60 acceptors (codenamed Mono-indene[C60] Mono-indene[C60] , Bis-indene[C60] ) were screened with the Solarmer polymers. These four polymers were screened and optimized with the indene class acceptors at both Plextronics and Solarmer. A combination was identified which produced 6.7% (internal measurement) with a Solarmer polymer and a Plextronics fullerene acceptor. This was accomplished primarily by improving the Voc as well as improving the current (Jsc) and FF.

  20. WOWBugs: Materials Development and Classroom Implementation of a Novel Organism.

    ERIC Educational Resources Information Center

    Koballa, Thomas R., Jr.; And Others

    The purpose of the WOWBug project was to promote "Melittobia digitata," a fruit-fly sized wasp, as a new organism for life science instruction and to determine the potential usefulness of the wasp to teach fundamental life science concepts. Fifty-five middle school teachers were introduced to the WOWBug and practiced with prototype activities in…

  1. Curriculum Materials for Vocational Youth Organizations: An Innovation Approach

    ERIC Educational Resources Information Center

    Feldhusen, John F.; And Others

    1977-01-01

    Leadership training is a form of instruction. As such, it should be guided by a model of instruction. Describes how the Three-Stage Model of Instruction (Feldhusen, Ames and Linden, 1973, 1974) was used to guide the development of thirteen units of leadership instruction for high school youth in vocational organizations. (Author/RK)

  2. Organic underlayer materials with exceptionally high thermal stability

    NASA Astrophysics Data System (ADS)

    Cheon, Hwan-Sung; Yoon, Kyong-Ho; Kim, Min-Soo; Oh, Sung Bae; Song, Jee-Yun; Tokareva, Nataliya; Kim, Jong-Seob; Chang, Tuwon

    2009-03-01

    Multilayer hardmask (MLHM) schemes have been implemented as an indispensable process for ArF lithography which continues to demand thinner photoresist films. There are many variations of MLHM and semiconductor manufacturers choose to adopt their own designs, depending on their specific needs and technical advances. The quad-layer stack consisting of photoresist, organic ARC, CVD Si hardmask, and spin-on carbon underlayer is one of them. Despite the need for wafer transporting between the spin track and CVD equipment, this scheme is attractive because it can avoid laborious elaboration of sophisticated etching chemistries for spin-on Si-ARC and carbon underlayer. One of the issues arising from the mixed film forming process is the thermal stability of carbon underlayer at high temperatures during the CVD process of the Si hardmask. Organic underlayer which shows high thermal stability is crucial for this mixed hardmask process. These types of thermally stable organic film can also be used for other applications such as the spacer patterning technique for pitch size shrinkage. In this paper, we discuss the development of organic resins with high thermal stability, their physical properties, and their lithographic behaviors in the MLHM schemes.

  3. Ideas for Organizing, Storing, and Using Equipment/Materials.

    ERIC Educational Resources Information Center

    United Cerebral Palsy Associations, Inc., Washington, DC.

    This document lists 55 ideas for organizing and lending computer equipment, switches, adapters, and software. The first section lists general organizational hints, including labeling of equipment, maintaining regular inventories, and establishing a crisis phone number and contact person to help people figure things out. The second section lists…

  4. 9 CFR 95.17 - Glands, organs, ox gall, and like materials; requirements for unrestricted entry.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 9 Animals and Animal Products 1 2012-01-01 2012-01-01 false Glands, organs, ox gall, and like... STRAW, OFFERED FOR ENTRY INTO THE UNITED STATES § 95.17 Glands, organs, ox gall, and like materials; requirements for unrestricted entry. Glands, organs, ox gall or bile, bone marrow, and various like...

  5. 9 CFR 95.17 - Glands, organs, ox gall, and like materials; requirements for unrestricted entry.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 9 Animals and Animal Products 1 2010-01-01 2010-01-01 false Glands, organs, ox gall, and like... STRAW, OFFERED FOR ENTRY INTO THE UNITED STATES § 95.17 Glands, organs, ox gall, and like materials; requirements for unrestricted entry. Glands, organs, ox gall or bile, bone marrow, and various like...

  6. 9 CFR 95.17 - Glands, organs, ox gall, and like materials; requirements for unrestricted entry.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 9 Animals and Animal Products 1 2011-01-01 2011-01-01 false Glands, organs, ox gall, and like... STRAW, OFFERED FOR ENTRY INTO THE UNITED STATES § 95.17 Glands, organs, ox gall, and like materials; requirements for unrestricted entry. Glands, organs, ox gall or bile, bone marrow, and various like...

  7. Electroactive materials for organic electronics: preparation strategies, structural aspects and characterization techniques.

    PubMed

    Pron, Adam; Gawrys, Pawel; Zagorska, Malgorzata; Djurado, David; Demadrille, Renaud

    2010-07-01

    This critical review discusses specific chemical and physicochemical requirements which must be met for organic compounds to be considered as promising materials for applications in organic electronics. Although emphasis is put on molecules and macromolecules suitable for fabrication of field effect transistors (FETs), a large fraction of the discussed compounds can also be applied in other organic or hybrid (organic-inorganic) electronic devices such as photodiodes, light emitting diodes, photovoltaic cells, etc. It should be of interest to chemists, physicists, material scientists and electrical engineers working in the domain of organic electronics (423 references). PMID:20393644

  8. Low Noise, High Detectivity Photodetectors based on Organic Materials

    NASA Astrophysics Data System (ADS)

    Guo, Fawen

    Organic photodetectors (OPDs) are potentially useful in many applications because of their light weight, flexibility and good form factors. Despite the high detectivities that have been frequently reported for OPDs recently, the application of these OPDs for weak light detection has been rarely demonstrated. In this thesis, low noise, high gain photodetectors based on organic and ZnO nanoparticles were proposed and demonstrated for highly sensitive UV light detection. The nanocomposite photodetector works in a hybrid mode of photodiode and photoconductor with the transition controlled by the UV light illumination. The nanocomposite detector shows two orders of magnitude higher sensitivity than silicon detectors in the UV range, which is the first time an organic, solution-processed detector has been shown to significantly outperform the inorganic photonic devices. In the fullerene-based photodetector, the dark-current has been successfully reduced by a cross-linked TPD (C-TPD) buffer layer. The high detectivity of 3.6 x 1011 cm Hz½ W-1 (Jones) at 370 nm and the wide Linear dynamic range (LDR) of 90 dB, along with a response speed faster than 20 kHz, suggests that the fullerene-based organic photodetectors proposed here can open the way for many potential applications. The ZnO nanoparticles have been introduced into the C-TPD buffer layer of the fullerene-based photodetector to increase the photoconductive gain and reduce the noise current. The peak external quantum efficiency (EQE) value of approximately 400% and the peak specific detectivity of 6.5 x 10 12 Jones at the wavelength of 390 nm, along with the record high LDR of 120 dB, enable the photodetector to be used in wide range of applications such as imaging, communication, and defense. The extremely high sensitivity of the photodetector also makes it particularly attractive for very weak light detection.

  9. Deterioration of organic packing materials commonly used in air biofiltration: effect of VOC-packing interactions.

    PubMed

    Lebrero, Raquel; Estrada, José M; Muñoz, Raúl; Quijano, Guillermo

    2014-05-01

    The abiotic deterioration of three conventional organic packing materials used in biofiltration (compost, wood bark and Macadamia nutshells) caused by their interaction with toluene (used as a model volatile organic compound) was here studied. The deterioration of the materials was evaluated in terms of structural damage, release of co-substrates and increase of the packing biodegradability. After 21 days of exposure to toluene, all packing materials released co-substrates able to support microbial growth, which were not released by the control materials not exposed to toluene. Likewise, the exposure to toluene increased the packing material biodegradability by 26% in wood bark, 20% in compost and 17% in Macadamia nutshells. Finally, scanning electron microscopy analysis confirmed the deterioration in the structure of the packing materials evaluated due to the exposure to toluene, Macadamia nutshells being the material with the highest resistance to volatile organic compound attack. PMID:24603032

  10. Organizing Learning Materials through Hierarchical Topic Maps: An Illustration through Chinese Herb Medication

    ERIC Educational Resources Information Center

    Shih, B.-J.; Shih, J.-L.; Chen, R.-L.

    2007-01-01

    This research aims to use hierarchical topic maps to compile digital learning material and to discuss its design and application possibilities. The system renders tremendous original assets and then embeds a self-organizing map (SOM) in the material database to produce topical learning materials, as in this case, an illustration through Chinese…

  11. Organic-inorganic hybrid materials: nanoparticle containing organogels with myriad applications.

    PubMed

    Peveler, William J; Bear, Joseph C; Southern, Paul; Parkin, Ivan P

    2014-11-28

    The synthesis of hybrid inorganic-organic materials from a single-component organogelator is reported. Varied functional inorganic materials were included and the resultant physico-chemical properties of the gels are presented. These materials are quick, versatile, can be cast into virtually any form, and the nanoparticles are easily reclaimed. PMID:25302345

  12. Abundance of Soil-Borne Entomopathogenic Fungi in Organic and Conventional Fields in the Midwestern USA with an Emphasis on the Effect of Herbicides and Fungicides on Fungal Persistence.

    PubMed

    Clifton, Eric H; Jaronski, Stefan T; Hodgson, Erin W; Gassmann, Aaron J

    2015-01-01

    Entomopathogenic fungi (EPF) are widespread in agricultural fields and help suppress crop pests. These natural enemies may be hindered by certain agronomic practices associated with conventional agriculture including the use of pesticides. We tested whether the abundance of EPF differed between organic and conventional fields, and whether specific cropping practices and soil properties were correlated with their abundance. In one year of the survey, soil from organic fields and accompanying margins had significantly more EPF than conventional fields and accompanying margins. Regression analysis revealed that the percentage of silt and the application of organic fertilizer were positively correlated with EPF abundance; but nitrogen concentration, tillage, conventional fields, and margins of conventional fields were negatively correlated with EPF abundance. A greenhouse experiment in which fungicides and herbicides were applied to the soil surface showed no significant effect on EPF. Though organic fields were perceived to be more suitable environments for EPF, abiotic factors and cropping practices such as tillage may have greater impacts on the abundance of EPF. Also, fungicides and herbicides may not be as toxic to soil-borne EPF as originally thought. PMID:26191815

  13. Abundance of Soil-Borne Entomopathogenic Fungi in Organic and Conventional Fields in the Midwestern USA with an Emphasis on the Effect of Herbicides and Fungicides on Fungal Persistence

    PubMed Central

    Clifton, Eric H.; Jaronski, Stefan T.; Hodgson, Erin W.; Gassmann, Aaron J.

    2015-01-01

    Entomopathogenic fungi (EPF) are widespread in agricultural fields and help suppress crop pests. These natural enemies may be hindered by certain agronomic practices associated with conventional agriculture including the use of pesticides. We tested whether the abundance of EPF differed between organic and conventional fields, and whether specific cropping practices and soil properties were correlated with their abundance. In one year of the survey, soil from organic fields and accompanying margins had significantly more EPF than conventional fields and accompanying margins. Regression analysis revealed that the percentage of silt and the application of organic fertilizer were positively correlated with EPF abundance; but nitrogen concentration, tillage, conventional fields, and margins of conventional fields were negatively correlated with EPF abundance. A greenhouse experiment in which fungicides and herbicides were applied to the soil surface showed no significant effect on EPF. Though organic fields were perceived to be more suitable environments for EPF, abiotic factors and cropping practices such as tillage may have greater impacts on the abundance of EPF. Also, fungicides and herbicides may not be as toxic to soil-borne EPF as originally thought. PMID:26191815

  14. The Suzaku Observation of the Nucleus of theRadio-Loud Active Galaxy Centaurus A: Constraints on Abundances of the Accreting Material

    SciTech Connect

    Markowitz, A.; Takahashi, T.; Watanabe, S.; Nakazawa, K.; Fukazawa, Y.; Kokubun, M.; Makishima, K.; Awaki, H.; Bamba, A.; Isobe, N.; Kataoka, J.; Madejski, G.; Mushotzky, R.; Okajima, T.; Ptak, A.; Reeves, J.N.; Ueda, Y.; Yamasaki, T.; Yaqoob, T.

    2007-06-27

    A Suzaku observation of the nucleus of the radio-loud AGN Centaurus A in 2005 has yielded a broadband spectrum spanning 0.3 to 250 keV. The net exposure times after screening were: 70 ks per X-ray Imaging Spectrometer (XIS) camera, 60.8 ks for the Hard X-ray Detector (HXD) PIN, and 17.1 ks for the HXD-GSO. The hard X-rays are fit by two power-laws of the same slope, absorbed by columns of 1.5 and 7 x 10{sup 23} cm{sup -2} respectively. The spectrum is consistent with previous suggestions that the power-law components are X-ray emission from the sub-pc VLBI jet and from Bondi accretion at the core, but it is also consistent with a partial covering interpretation. The soft band is dominated by thermal emission from the diffuse plasma and is fit well by a two-temperature vapec model, plus a third power-law component to account for scattered nuclear emission, jet emission, and emission from X-ray Binaries and other point sources. Narrow fluorescent emission lines from Fe, Si, S, Ar, Ca and Ni are detected. The Fe K{alpha} line width yields a 200 light-day lower limit on the distance from the black hole to the line-emitting gas. Fe, Ca, and S K-shell absorption edges are detected. Elemental abundances are constrained via absorption edge depths and strengths of the fluorescent and diffuse plasma emission lines. The high metallicity ([Fe/H]=+0.1) of the circumnuclear material suggests that it could not have originated in the relatively metal-poor outer halo unless enrichment by local star formation has occurred. Relative abundances are consistent with enrichment from Type II and Ia supernovae.

  15. Highly Efficient Organic Hole Transporting Materials for Perovskite and Organic Solar Cells with Long-Term Stability.

    PubMed

    Reddy, Saripally Sudhaker; Gunasekar, Kumarasamy; Heo, Jin Hyuck; Im, Sang Hyuk; Kim, Chang Su; Kim, Dong-Ho; Moon, Jong Hun; Lee, Jin Yong; Song, Myungkwan; Jin, Sung-Ho

    2016-01-27

    Small molecules based on N-atom-linked phenylcarbazole-fluorene as the main scaffold, end-capped with spirobifluorene derivatives, are developed as organic hole-transporting materials for highly efficient perovskite solar cells (PSCs) and bulk heterojunction (BHJ) inverted organic solar cells (IOSCs). The CzPAF-SBF-based devices show remarkable device performance with excellent long-term stability in PSCs and BHJ IOSCs with a maximum PCE of 17.21% and 7.93%, respectively. PMID:26619180

  16. Fuel pellet and process for making it by shaping under pressure an organic fibrous material

    SciTech Connect

    Gunnerman, R.W.

    1981-12-29

    An organic fibrous material such as bagasse, tree bark, sawdust, straw, peat moss, tree twigs and the like is mixed with a waxy material which is compatible with natural waxy substances contained by the organic fibrous material. The mixture is shaped into a substantially symmetrical pellet having a density of at least about 62.5 pounds per cubic foot with a maximum dimension in section of one-half inch or less in a pelletizing mill under an applied pressure whereby the natural waxy substance contained by the organic fibrous material are exuded to the surface of the resulting pellet and mixed with the added waxy materials to form a substantially uniform continuous coating over the surfaces of an organic fibrous core. The coated pellet releases more energy at a faster rate than the uncoated core when burned alone.

  17. Viscosity of α-pinene secondary organic material and implications for particle growth and reactivity

    NASA Astrophysics Data System (ADS)

    Renbaum-Wolff, Lindsay; Grayson, James W.; Kuwata, Mikinori; Bateman, Adam P.; Sellier, Mathieu; Murray, Benjamin J.; Shilling, John; Martin, Scot T.; Bertram, Allan K.

    2013-04-01

    Secondary organic particles are abundant in the troposphere, and may play an important role in climate, air quality, and health. Viscosity is a physical property of particles that is poorly understood and may influence particle sizes and concentrations in the troposphere, as well as reaction rates with various atmospheric oxidants. In order to predict the effects of particle viscosity on various atmospheric processes, the viscosities must be quantified. A major obstacle to measuring viscosities of atmospheric or environmental chamber samples is the small sample volumes (typically on the order of milligrams after long collection times). The minimum sample volumes required for current microviscometry techniques are on the order of 10's of μL's. Those techniques, however, are limited to measuring viscosities <0.1 Pa s, in the low viscosity liquid regime. The viscometers currently available to measure higher viscosities require much greater sample volumes, which are not realistically achievable in any atmospheric sampling or chamber experiments. Presented here are two novel approaches to measuring the viscosity of environmental chamber and atmospheric samples, which are capable of measuring a wide range of viscosities using significantly less than 1mg of material, and applicable across the ambient tropospheric RH range. The first is a bead-mobility technique, where small (~1μm), insoluble beads are observed as they circulate within 20-50 μm particles. The second is a poke-flow technique, whereby 20-70 μm particles are poked with a needle, and the flow rate of these particles after poking is used to determine viscosity. These techniques not only provide visual evidence that the water-soluble fraction of atmospheric samples behave as semi-solids or solids, but also quantitative information as to their viscosities.

  18. Using an organic radical precursor as an electron injection material for efficient and stable organic light-emitting diodes.

    PubMed

    Bin, Zhengyang; Liu, Ziyang; Wei, Pengcheng; Duan, Lian; Qiu, Yong

    2016-04-29

    Materials with strong reducibility have been used as electron injection layers (EILs) to lower the work function of cathodes and reduce the driving voltage of organic light-emitting diodes (OLEDs). However, the most prominent electron injection materials presented so far are high-temperature-evaporable inorganic salts based on alkaline metals, which suffer from a high tendency of metal diffusion throughout the organic layer and thus reduce the device efficiency and stability. Here, we introduce a new kind of EIL based on a stable precursor of a strongly reducing organic radical. By using an organic precursor, we are able to take the advantage of the low-evaporation-temperature and avoid the problem of metal diffusion, thus improving the device efficiency and stability. Ultraviolet photoelectron spectroscopy (UPS) study indicates that inserting a thin layer of organic radical between the electron transport layer and cathode could greatly reduce the electron injection barrier due to the strong interaction of radical with cathode and the electron transporting material. As a result, OLEDs with an organic radical as the EIL showed a 25.2% higher efficiency and 2.2 times longer lifetime than the control device with conventional LiF as the EIL. PMID:26988713

  19. Using an organic radical precursor as an electron injection material for efficient and stable organic light-emitting diodes

    NASA Astrophysics Data System (ADS)

    Bin, Zhengyang; Liu, Ziyang; Wei, Pengcheng; Duan, Lian; Qiu, Yong

    2016-04-01

    Materials with strong reducibility have been used as electron injection layers (EILs) to lower the work function of cathodes and reduce the driving voltage of organic light-emitting diodes (OLEDs). However, the most prominent electron injection materials presented so far are high-temperature-evaporable inorganic salts based on alkaline metals, which suffer from a high tendency of metal diffusion throughout the organic layer and thus reduce the device efficiency and stability. Here, we introduce a new kind of EIL based on a stable precursor of a strongly reducing organic radical. By using an organic precursor, we are able to take the advantage of the low-evaporation-temperature and avoid the problem of metal diffusion, thus improving the device efficiency and stability. Ultraviolet photoelectron spectroscopy (UPS) study indicates that inserting a thin layer of organic radical between the electron transport layer and cathode could greatly reduce the electron injection barrier due to the strong interaction of radical with cathode and the electron transporting material. As a result, OLEDs with an organic radical as the EIL showed a 25.2% higher efficiency and 2.2 times longer lifetime than the control device with conventional LiF as the EIL.

  20. Abundance of volatile and organic species in intermediate temperature fluids from the Von Damm and Piccard deep sea hydrothermal fields, Mid-Cayman Rise

    NASA Astrophysics Data System (ADS)

    McDermott, J. M.; Seewald, J.; Reeves, E. P.; German, C. R.; Sylva, S. P.; Klein, F.

    2012-12-01

    vent fluids, and imply the presence of a CO2 sink. Von Damm fluid CO2/CH4 ratios are relatively constant at 1.0 to 1.5 (mol/mol) in the higher temperature fluids, and are low compared with CO2/CH4 ratios of 200 to 250 (mol/mol) in the higher temperature Piccard fluids. All vent fluids at Von Damm are enriched in CH4 and longer-chain n-alkanes. Von Damm fluid H2 and H2S abundances are consistent with those at Rainbow and other ultramafic-influenced systems. At the Von Damm vent field, H2 shows non-conservative behavior in intermediate fluids at temperatures ≤114 °C. Such behavior is consistent with previous studies, which attributed non-conservative H2 behavior in ~30 °C vent fluids to microbial consumption (e.g. Von Damm and Lilley, 2004). Similar activity may be occurring at Von Damm. At Piccard, H2 shows non-conservative mixing behavior at temperatures ≤149 °C. H2 depletion at Piccard occurs at higher temperatures than at Von Damm, in excess of the currently known limit for life at 122 °C (Takei et al., 2008), suggesting that abiotic as well as microbial processes may be affecting H2 abundance. Methylated organic compounds, including methanethiol and methanol, were also observed in vent fluids at Piccard and Von Damm, and further organic compound analyses are ongoing.

  1. Polytellurophenes as Solution Processable Materials for Applications in Organic Electronics

    NASA Astrophysics Data System (ADS)

    Jahnke, Ashlee Anne

    With very few previous publications on polytellurophenes prior to 2009, this is a largely unexplored class of conjugated polymers. This thesis details investigations into two types of tellurophene polymers. The synthesis of four novel tellurophene containing polymers is described and the characterization of their optical, solid-state, and electronic properties is discussed. The first chapter provides an introduction to the history of the field of polytellurophenes and provides context for the work presented in this thesis. The second chapter describes the synthesis of a novel bitellurophene monomer and its use in palladium-catalyzed polymerization. Once synthesized, the polymer is used to explore the unique chemistry of tellurium and its ability to form coordination species with bromine. Upon treatment with elemental bromine, changes in the optical properties of the system are observed. In chapter three, the synthesis of the first examples of soluble tellurophene homopolymers is presented. These poly(3-alkyltellurophene)s are solution processable materials and are fully characterized in solution and the solid-state. Chapter four describes further studies into the thin-film morphology of the materials presented in chapter three. Furthermore, semiconductor:insulator blends are prepared using poly(3-alkyltellurophene)s and high-density polyethylene. Taking advantage of the elemental contrast provided by the tellurium heavy atom, the micro- and nanostructure of the blend thin-films are investigated with various microscopy techniques providing insight into these types of blends that was previously unavailable. In the final chapter, the performance of these materials in thin-film field-effect transistors was investigated.

  2. Sucrose: A prospering and sustainable organic raw material.

    PubMed

    Peters, Siegfried; Rose, Thomas; Moser, Matthias

    2010-01-01

    Sucrose (alpha-D-glucopyranosyl-(1-->2)-beta-D-fructofuranoside) is an inexpensive chemical produced by sugar cane and sugar beet cultivation. Chemical and/or biochemical transformations convert it into highly valuable synthetic intermediates such as 5-hydroxymethylfurfural (HMF), bioethylene, 1,2-propylene glycol and levulinic acid. Sucrose can also be converted into biodegradable polymers such as polyesters and polyurethanes, as well as into novel carbohydrates such as isomaltulose, trehalulose, inulin, levan, Neo-amylose, and dextran, highly valuable additives for food and cosmetics and materials for separation and purification technologies. PMID:21626746

  3. Sucrose: A Prospering and Sustainable Organic Raw Material

    NASA Astrophysics Data System (ADS)

    Peters, Siegfried; Rose, Thomas; Moser, Matthias

    Sucrose (α-d-glucopyranosyl-(1→2)-β-d-fructofuranoside) is an inexpensive chemical produced by sugar cane and sugar beet cultivation. Chemical and/or biochemical transformations convert it into highly valuable synthetic intermediates such as 5-hydroxymethylfurfural (HMF), bioethylene, 1,2-propylene glycol and levulinic acid. Sucrose can also be converted into biodegradable polymers such as polyesters and polyurethanes, as well as into novel carbohydrates such as isomaltulose, trehalulose, inulin, levan, Neo-amylose, and dextran, highly valuable additives for food and cosmetics and materials for separation and purification technologies.

  4. Containerless synthesis of amorphous and nanophase organic materials

    DOEpatents

    Benmore, Chris J.; Weber, Johann R.

    2016-05-03

    The invention provides a method for producing a mixture of amorphous compounds, the method comprising supplying a solution containing the compounds; and allowing at least a portion of the solvent of the solution to evaporate while preventing the solute of the solution from contacting a nucleation point. Also provided is a method for transforming solids to amorphous material, the method comprising heating the solids in an environment to form a melt, wherein the environment contains no nucleation points; and cooling the melt in the environment.

  5. Hybrid exciton recombination dynamics in inorganic-organic materials

    SciTech Connect

    Mastour, N. Bouchriha, H.

    2013-12-16

    A systematic analysis of hybrid Frenkel–Wannier–Mott excitons recombination dynamics in nanocomposite material (organic–inorganic) is performed. A theoretical model based on the rate equation is used in the calculation of the light intensity and relative quantum efficiency. Numerical results have been presented for low and high concentration of quantum dots (Qds). Our results show that the light emission and relative quantum efficiency are significantly enhanced by incorporation of Qds in polymer matrix. Moreover our calculations were found to be in good agreement with the experimental data.

  6. Influence of dissolved organic materials on turbid water optical properties and remote-sensing reflectance

    NASA Technical Reports Server (NTRS)

    Witte, W. G.; Whitlock, C. H.; Harriss, R. C.; Usry, J. W.; Poole, L. R.; Houghton, W. M.; Morris, W. D.; Gurganus, E. A.

    1982-01-01

    The effects of dissolved organic materials on turbid-water optical properties are assessed, by means of field measurements and laboratory simulations in which upwelled reflectance, attenuation, absorption, and backscatter spectral properties at wavelengths from 450 to 800 nm are examined in relation to water chemistry. The data show that dissolved organic materials decrease upwelled reflectance from turbid waters, and that the decrease in reflectance is a nonlinear function of concentration with the largest gradients at low carbon concentrations, depending on wavelength. Upwelled reflectance is found to be highly correlated with two backscatter-absorption parameters used in some optical models, which are nonlinear with dissolved organic material concentration change.

  7. Quantitative Probes of Electron-Phonon Coupling in an Organic Charge-Transfer Material

    NASA Astrophysics Data System (ADS)

    Rury, Aaron; Sorenson, Shayne; Driscoll, Eric; Dawlaty, Jahan

    While organic charge transfer (CT) materials may provide alternatives to inorganic materials in electronics and photonics applications, properties central to applications remain understudied in these organic materials. Specifically, electron-phonon coupling plays a pivotal role in electronic applications yet this coupling in CT materials remains difficult to directly characterize. To better understand the suitability of organic CT materials for electronic applications, we have devised an experimental technique that can directly assess electron-phonon coupling in a model organic CT material. Upon non-resonant interaction with an ultrafast laser pulse, we show that coherent excitation of Raman-active lattice vibrations of quinhydrone, a 1:1 co-crystal of the hydroquinone and p-benzoquinone, modulates the energies of electronic transitions probed by a white light pulse. Using a well-established theoretical framework of vibrational quantum beat spectra across the probe bandwidth, we quantitatively extract the parameters describing these electronic transitions to characterize electron-phonon coupling in this material. In conjunction with temperature-dependent resonance Raman measurements, we assess the hypothesis that several sharp transitions in the near-IR correspond to previously unknown excitonic states of this material. These results and their interpretation set the foundation for further elucidation of the one of the most important parameters in the application of organic charge-transfer materials to electronics and photonics.

  8. Interlaboratory study of a method for determining nonvolatile organic carbon in aquifer materials

    USGS Publications Warehouse

    Caughey, M.E.; Barcelona, M.J.; Powell, R.M.; Cahill, R.A.; Gron, C.; Lawrenz, D.; Meschi, P.L.

    1995-01-01

    The organic carbon fraction in aquifer materials exerts a major influence on the subsurface mobilities of organic and organic-associated contaminants. The spatial distribution of total organic carbon (TOC) in aquifer materials must be determined before the transport of hydrophobic organic pollutants in aquifers can be modeled accurately. Previous interlaboratory studies showed that it is difficult to measure TOC concentrations 1%. We have tested a new analytical method designed to improve the accuracy and precision of nonvolatile TOC quantitation in geologic materials that also contain carbonate minerals. Four authentic aquifer materials and one NIST standard reference material were selected as test materials for a blind collaborative study. Nonvolatile TOC in these materials ranged from 0.05 to 1.4%, while TIC ranged from 0.46 to 12.6%. Sample replicates were digested with sulfurous acid, dried at 40??C, and then combusted at 950??C using LECO or UIC instruments. For the three test materials that contained >2% TIC, incomplete acidification resulted in a systematic positive bias of TOC values reported by five of the six laboratories that used the test method. Participants did not have enough time to become proficient with the new method before they analyzed the test materials. A seventh laboratory successfully used an alternative method that analyzed separate liquid and solid fractions of the acidified sample residues. ?? 1995 Springer-Verlag.

  9. Short interspersed nuclear elements (SINEs) are abundant in Solanaceae and have a family-specific impact on gene structure and genome organization.

    PubMed

    Seibt, Kathrin M; Wenke, Torsten; Muders, Katja; Truberg, Bernd; Schmidt, Thomas

    2016-05-01

    Short interspersed nuclear elements (SINEs) are highly abundant non-autonomous retrotransposons that are widespread in plants. They are short in size, non-coding, show high sequence diversity, and are therefore mostly not or not correctly annotated in plant genome sequences. Hence, comparative studies on genomic SINE populations are rare. To explore the structural organization and impact of SINEs, we comparatively investigated the genome sequences of the Solanaceae species potato (Solanum tuberosum), tomato (Solanum lycopersicum), wild tomato (Solanum pennellii), and two pepper cultivars (Capsicum annuum). Based on 8.5 Gbp sequence data, we annotated 82 983 SINE copies belonging to 10 families and subfamilies on a base pair level. Solanaceae SINEs are dispersed over all chromosomes with enrichments in distal regions. Depending on the genome assemblies and gene predictions, 30% of all SINE copies are associated with genes, particularly frequent in introns and untranslated regions (UTRs). The close association with genes is family specific. More than 10% of all genes annotated in the Solanaceae species investigated contain at least one SINE insertion, and we found genes harbouring up to 16 SINE copies. We demonstrate the involvement of SINEs in gene and genome evolution including the donation of splice sites, start and stop codons and exons to genes, enlargement of introns and UTRs, generation of tandem-like duplications and transduction of adjacent sequence regions. PMID:26996788

  10. A New Tool for NMR Crystallography: Complete (13)C/(15)N Assignment of Organic Molecules at Natural Isotopic Abundance Using DNP-Enhanced Solid-State NMR.

    PubMed

    Märker, Katharina; Pingret, Morgane; Mouesca, Jean-Marie; Gasparutto, Didier; Hediger, Sabine; De Paëpe, Gaël

    2015-11-01

    NMR crystallography of organic molecules at natural isotopic abundance (NA) strongly relies on the comparison of assigned experimental and computed NMR chemical shifts. However, a broad applicability of this approach is often hampered by the still limited (1)H resolution and/or difficulties in assigning (13)C and (15)N resonances without the use of structure-based chemical shift calculations. As shown here, such difficulties can be overcome by (13)C-(13)C and for the first time (15)N-(13)C correlation experiments, recorded with the help of dynamic nuclear polarization. We present the complete de novo (13)C and (15)N resonance assignment at NA of a self-assembled 2'-deoxyguanosine derivative presenting two different molecules in the asymmetric crystallographic unit cell. This de novo assignment method is exclusively based on aforementioned correlation spectra and is an important addition to the NMR crystallography approach, rendering firstly (1)H assignment straightforward, and being secondly a prerequisite for distance measurements with solid-state NMR. PMID:26485326

  11. Novel High Efficient Organic Photovoltaic Materials: Final Summary of Research

    NASA Technical Reports Server (NTRS)

    Sun, Sam

    2002-01-01

    The objectives and goals of this project were to investigate and develop high efficient, lightweight, and cost effective materials for potential photovoltaic applications, such as solar energy conversion or photo detector devices. Specifically, as described in the original project proposal, the target material to be developed was a block copolymer system containing an electron donating (or p-type) conjugated polymer block coupled to an electron withdrawing (or n-type) conjugated polymer block through a non-conjugated bridge unit. Due to several special requirements of the targeted block copolymer systems, such as electron donating and withdrawing substituents, conjugated block structures, processing requirement, stability requirement, size controllability, phase separation and self ordering requirement, etc., many traditional or commonly used block copolymer synthetic schemes are not suitable for this system. Therefore, the investigation and development of applicable and effective synthetic protocols became the most critical and challenging part of this project. During the entire project period, and despite the lack of a proposed synthetic polymer postdoctoral research associate due to severe shortage of qualified personnel in the field, several important accomplishments were achieved in this project and are briefly listed and elaborated. A more detailed research and experimental data is listed in the Appendix.

  12. Hybrid metal organic scintillator materials system and particle detector

    DOEpatents

    Bauer, Christina A.; Allendorf, Mark D.; Doty, F. Patrick; Simmons, Blake A.

    2011-07-26

    We describe the preparation and characterization of two zinc hybrid luminescent structures based on the flexible and emissive linker molecule, trans-(4-R,4'-R') stilbene, where R and R' are mono- or poly-coordinating groups, which retain their luminescence within these solid materials. For example, reaction of trans-4,4'-stilbenedicarboxylic acid and zinc nitrate in the solvent dimethylformamide (DMF) yielded a dense 2-D network featuring zinc in both octahedral and tetrahedral coordination environments connected by trans-stilbene links. Similar reaction in diethylformamide (DEF) at higher temperatures resulted in a porous, 3-D framework structure consisting of two interpenetrating cubic lattices, each featuring basic to zinc carboxylate vertices joined by trans-stilbene, analogous to the isoreticular MOF (IRMOF) series. We demonstrate that the optical properties of both embodiments correlate directly with the local ligand environments observed in the crystal structures. We further demonstrate that these materials produce high luminescent response to proton radiation and high radiation tolerance relative to prior scintillators. These features can be used to create sophisticated scintillating detection sensors.

  13. Boron Subphthalocyanines as Triplet Harvesting Materials within Organic Photovoltaics.

    PubMed

    Castrucci, Jeffrey S; Josey, David S; Thibau, Emmanuel; Lu, Zheng-Hong; Bender, Timothy P

    2015-08-01

    Singlet fission, the generation of two excited triplet states from a single absorbed photon, is currently an area of significant interest to photovoltaic researchers. In this Letter, we outline how a polychlorinated boron subphthalocyanine, previously hypothesized to be an effective harvester of singlet fission derived triplets from pentacene, is relatively efficient at facilitating the process. As expected, we found a major increase in photocurrent generation at the expense of device voltage. For a direct point of comparison, we also have paired the same polychlorinated boron subphthalocyanine with α-sexithiophene to probe the alternative technique of complementary absorption engineering. The sum of these efforts have let us present new guidelines for the molecular design of boron subphthalocyanine for organic photovoltaic applications. PMID:26267212

  14. Self-organization in periodically sheared granular materials

    NASA Astrophysics Data System (ADS)

    Wilken, Sam; Hunter, Gary L.; Chaikin, Paul M.

    2015-03-01

    Self-organization as a result of periodic shear is becoming a feature observed in an increasing number of systems. In our experiments, we enforce cyclic shear on a three dimensional system of non-Brownian particles to investigate the global packing behavior of the granular assembly. By starting with a dilated, loosely packed system and measuring the packing fraction after each shear cycle, we find the system compacts to reach a steady state with a well defined packing fraction. The shear amplitude determines the steady state packing fraction, where large amplitude shear produces a lower packing density and small amplitude shear produces a higher packing density. We also study the phase diagram of this system which exhibits caged motion and a transition to vorticity.

  15. Grown organic matter as a fuel raw material resource

    NASA Technical Reports Server (NTRS)

    Roller, W. L.; Keener, H. M.; Kline, R. D.; Mederski, H. J.; Curry, R. B.

    1975-01-01

    An extensive search was made on biomass production from the standpoint of climatic zones, water, nutrients, costs and energy requirements for many species. No exotic species were uncovered that gave hope for a bonanza of biomass production under culture, location, and management markedly different from those of existing agricultural concepts. A simulation analysis of biomass production was carried out for six species using conventional production methods, including their production costs and energy requirements. These estimates were compared with data on food, fiber, and feed production. The alternative possibility of using residues from food, feed, or lumber was evaluated. It was concluded that great doubt must be cast on the feasibility of producing grown organic matter for fuel, in competition with food, feed, or fiber. The feasibility of collecting residues may be nearer, but the competition for the residues for return to the soil or cellulosic production is formidable.

  16. 3D printing of natural organic materials by photochemistry

    NASA Astrophysics Data System (ADS)

    Da Silva Gonçalves, Joyce Laura; Valandro, Silvano Rodrigo; Wu, Hsiu-Fen; Lee, Yi-Hsiung; Mettra, Bastien; Monnereau, Cyrille; Schmitt Cavalheiro, Carla Cristina; Pawlicka, Agnieszka; Focsan, Monica; Lin, Chih-Lang; Baldeck, Patrice L.

    2016-03-01

    In previous works, we have used two-photon induced photochemistry to fabricate 3D microstructures based on proteins, anti-bodies, and enzymes for different types of bio-applications. Among them, we can cite collagen lines to guide the movement of living cells, peptide modified GFP biosensing pads to detect Gram positive bacteria, anti-body pads to determine the type of red blood cells, and trypsin columns in a microfluidic channel to obtain a real time biochemical micro-reactor. In this paper, we report for the first time on two-photon 3D microfabrication of DNA material. We also present our preliminary results on using a commercial 3D printer based on a video projector to polymerize slicing layers of gelatine-objects.

  17. Organization and diffusion in biological and material fabrication problems

    NASA Astrophysics Data System (ADS)

    Mangan, Niall Mari

    anhydrase and RuBisCO in a smaller volume raises the concentration of carbon dioxide around RuBisCO by switching from a regime where the carbonic anhydrase is saturated to non-saturated. Hyper-doping with femto-second lasers offers a versatile method for creating new materials including semi-conductor materials doped at beyond the equilibrium solubility limit. Silicon hyper-doped with sulfur has been shown to absorb highly in the infra-red region. Hyper-doped silicon already is already used in night-vision infra-red sensors and is being explored for other applications such as photovoltaics. Being able to finely tune the dopant profile in the material will allow us to achieve more efficient and effective devices. To better control the doping profile, we develop a model which correctly represents the physics of melting of Si and diffusion of dopant into the material. The thermal and solute diffusion model produces melt dynamics and dopant profiles consistent with experimental data. We present the results of numerical simulations. We identify two distinct mechanisms which account for the characteristic dopant profiles in experiments. A change in laser absorption such that the melt depth increases or a change in the mechanism of dopant integration from an "instant surface dose" to a surface flux can both account for changes in dopant profile with subsequent laser pulses.

  18. Photochemical aging of light-absorbing secondary organic aerosol material.

    PubMed

    Sareen, Neha; Moussa, Samar G; McNeill, V Faye

    2013-04-11

    Dark reactions of methylglyoxal with NH4(+) in aqueous aerosols yield light-absorbing and surface-active products that can influence the physical properties of the particles. Little is known about how the product mixture and its optical properties will change due to photolysis as well as oxidative aging by O3 and OH in the atmosphere. Here, we report the results of kinetics and product studies of the photochemical aging of aerosols formed by atomizing aqueous solutions of methylglyoxal and ammonium sulfate. Experiments were performed using aerosol flow tube reactors coupled with an aerosol chemical ionization mass spectrometer (Aerosol-CIMS) for monitoring gas- and particle-phase compositions. Particles were also impacted onto quartz windows in order to assess changes in their UV-visible absorption upon oxidation. Photooxidation of the aerosols leads to the formation of small, volatile organic acids including formic acid, acetic acid, and glyoxylic acid. The atmospheric lifetime of these species during the daytime is predicted to be on the order of minutes, with photolysis being an important mechanism of degradation. The lifetime with respect to O3 oxidation was observed to be on the order of hours. O3 oxidation also leads to a net increase in light absorption by the particles due to the formation of additional carbonyl compounds. Our results are consistent with field observations of high brown carbon absorption in the early morning. PMID:23506538

  19. Nanostructured organic electronic materials: Synthesis and sensor applications

    NASA Astrophysics Data System (ADS)

    Dua, Vineet

    2009-12-01

    This study is an investigation into (a) the process by which one obtains bulk quantities of nanofibers of parent polythiophene, (b) in-situ deposition of nanofibers of polythiophene on flexible substrate and its application in vapor sensing, and (c) inkjet printing of graphene on flexible substrate and its application as a detector. (a) The 2 nd chapter of the thesis is an extension of "seeding" method from aqueous to organic solvents to synthesize parent polythiophene nanofibers. Bulk quantities of parent polythiophene nanofibers were synthesized in one step using catalytic amounts of freeze dried V2O5. This work is published in Chemistry Letters 2008 37(5), 526--527. (b) The 3rd chapter deals with in-situ films of polythiophene nanofibers on plastic substrates. In this a one step method to directly deposit nanofibers of parent polythiophene on flexible substrate is discussed. These films show a reversible detection of highly oxidizing vapors such as NO2, Cl2 and SO 2 at ppb levels under ambient conditions. This work is published in Macromolecules 2009, 42, 5414--5415. (c) The 4 th chapter describes the synthesis of reduced graphene oxide (RGO) using a mild reducing agent ascorbic acid (Vitamin C) rather than traditionally used harsh reducing agents (N2H4). Dispersions of RGO were inkjet printed on flexible substrate and has been shown to detect aggressive vapors NO2 and Cl2 at ambient conditions. This work is accepted for publication in Angewandte Chemie (Nov 2009).

  20. Purchasing and Materials Management Organization, Sandia National Laboratories annual report, fiscal year 1993

    SciTech Connect

    Martin, D.R.

    1994-02-01

    This report summarizes the purchasing and transportation activities of the Purchasing and Materials Management Organization for Fiscal Year 1993. Activities for both the New Mexico and California locations are included.

  1. EVALUATION OF THREE FISH SPECIES AS BIOASSAY ORGANISMS FOR DREDGED MATERIAL TESTING

    EPA Science Inventory

    Three fish species, Cyprinodon variegatus, Fundulus similis, and Menidia menidia, were evaluated to determine which is most suitable as a bioassay organism for solid phase testing of dredged material. Acute toxicity and bioaccumulation of polychlorinated biphenyls (PCBs) were mon...

  2. Metal-organic framework materials based on icosahedral boranes and carboranes

    DOEpatents

    Mirkin, Chad A.; Hupp, Joseph T.; Farha, Omar K.; Spokoyny, Alexander M.; Mulfort, Karen L.

    2010-11-02

    Disclosed herein are metal-organic frameworks of metals and boron rich ligands, such as carboranes and icosahedral boranes. Methods of synthesizing and using these materials in gas uptake are disclosed.

  3. Evaluation and Validation of Organic Materials for Advanced Stirling Convertors (ASCs): Overview

    NASA Technical Reports Server (NTRS)

    Shin, Euy-Sik Eugene

    2015-01-01

    Various organic materials are used as essential parts in Stirling Convertors for their unique properties and functionalities such as bonding, potting, sealing, thread locking, insulation, and lubrication. More efficient Advanced Stirling Convertors (ASC) are being developed for future space applications especially with a long mission cycle, sometimes up to 17 years, such as deep space exploration or lunar surface power or Mars rovers, and others. Thus, performance, durability, and reliability of those organics should be critically evaluated in every possible material-process-fabrication-service environment relations based on their mission specifications. In general, thermal stability, radiation hardness, outgassing, and material compatibility of the selected organics have been systematically evaluated while their process and fabrication conditions and procedures were being optimized. Service environment-simulated long term aging tests up to 4 years were performed as a function of temperature for durability assessment of the most critical organic material systems.

  4. REFERENCE MATERIALS AND QUALITY ASSURANCE FOR THE CHARACTERIZATION OF ORGANIC COMPOUNDS IN PARTICULATE MATTER

    EPA Science Inventory

    One of the first environmental matrix Standard Reference Materials (SRMs) developed by the National Institute of Standards and Technology (NIST) for determination of organic species was SRM 1649 Urban Dust, ambient total suspended particulate matter (PM) collected in Washington D...

  5. Hybrid Organic-Inorganic Coordination Complexes as Tunable Optical Response Materials.

    PubMed

    Travis, Will; Knapp, Caroline E; Savory, Christopher N; Ganose, Alex M; Kafourou, Panagiota; Song, Xingchi; Sharif, Zainab; Cockcroft, Jeremy K; Scanlon, David O; Bronstein, Hugo; Palgrave, Robert G

    2016-04-01

    Novel lead and bismuth dipyrido complexes have been synthesized and characterized by single-crystal X-ray diffraction, which shows their structures to be directed by highly oriented π-stacking of planar fully conjugated organic ligands. Optical band gaps are influenced by the identity of both the organic and inorganic component. Density functional theory calculations show optical excitation leads to exciton separation between inorganic and organic components. Using UV-vis, photoluminescence, and X-ray photoemission spectroscopies, we have determined the materials' frontier energy levels and show their suitability for photovoltaic device fabrication by use of electron- and hole-transport materials such as TiO2 and spiro-OMeTAD respectively. Such organic/inorganic hybrid materials promise greater electronic tunability than the inflexible methylammonium lead iodide structure through variation of both the metal and organic components. PMID:26974692

  6. Implantation blocking characteristics study of organic BARC materials

    NASA Astrophysics Data System (ADS)

    Kim, Myoung-Soo; Seo, Jae-Wook; Shim, Kew-Chan; Jin, Seung-Woo; Kim, Hak-Joon; Gil, Myung-Goon; Song, Yong-Wook

    2006-03-01

    In this study, the four different types of ArF and KrF OBARC have been evaluated to know the implantation blocking and gap fill performance for 80nm node device application. The boron implantation conditions of 11B and 49BF2 are processed and the minimum energy for implantation blocking of these OBARC are obtained by SIMS analysis. The minimum energy of ArF and KrF OBARC are about 13.0KeV and 15.0KeV, respectively. The chemical density of each OBARC is also calculated from the minimum blocking energy. Their values of ArF and KrF OBARC are about 0.8g/cm 3 and 1.0g/cm 3, respectively. The minimum energy trends among the tested materials show the almost similar results with those of chemical density as expected. Even though the OBARC are composed of the similar chemical structure, they induce the different chemical density because of their own molecular weight and other additional structure as like chromophore. Both of KrF and ArF OBARC show the good gap fill performance on 0.2μm size of via substrate and real topology pattern without void. It seems that the gap fill property is not much affected by the chemical structure or molecular weight of OBARC. It is thought that OBARC is an effective material for gap fill application than other resists, especially for deep topology patterns. In general, the etch rate of OBARC is slightly faster than that of ArF resist or similar with that in this experimental condition. The OBARC having high chemical density shows the slower etch rate and that of OBARC is inversely proportional to the chemical density of it. Therefore, it is confirmed that the OBARC is able to apply for implantation blocking purpose without gap fill void in real device below 80nm, since they have the good characteristics for gap fill, reflectivity control from substrate and implantation blocking property at a certain coating thickness.

  7. Hybrid Organic/Inorganic Materials Depth Profiling Using Low Energy Cesium Ions

    NASA Astrophysics Data System (ADS)

    Noël, Céline; Houssiau, Laurent

    2016-02-01

    The structures developed in organic electronics, such as organic light emitting diodes (OLEDs) or organic photovoltaics (OPVs) devices always involve hybrid interfaces, joining metal or oxide layers with organic layers. No satisfactory method to probe these hybrid interfaces physical chemistry currently exists. One promising way to analyze such interfaces is to use in situ ion beam etching, but this requires ion beams able to depth profile both inorganic and organic layers. Mono- or diatomic ion beams commonly used to depth profile inorganic materials usually perform badly on organics, while cluster ion beams perform excellently on organics but yield poor results when organics and inorganics are mixed. Conversely, low energy Cs+ beams (<500 eV) allow organic and inorganic materials depth profiling with comparable erosion rates. This paper shows a successful depth profiling of a model hybrid system made of metallic (Au, Cr) and organic (tyrosine) layers, sputtered with 500 eV Cs+ ions. Tyrosine layers capped with metallic overlayers are depth profiled easily, with high intensities for the characteristic molecular ions and other specific fragments. Metallic Au or Cr atoms are recoiled into the organic layer where they cause some damage near the hybrid interface as well as changes in the erosion rate. However, these recoil implanted metallic atoms do not appear to severely degrade the depth profile overall quality. This first successful hybrid depth profiling report opens new possibilities for the study of OLEDs, organic solar cells, or other hybrid devices.

  8. Hybrid Organic/Inorganic Materials Depth Profiling Using Low Energy Cesium Ions.

    PubMed

    Noël, Céline; Houssiau, Laurent

    2016-05-01

    The structures developed in organic electronics, such as organic light emitting diodes (OLEDs) or organic photovoltaics (OPVs) devices always involve hybrid interfaces, joining metal or oxide layers with organic layers. No satisfactory method to probe these hybrid interfaces physical chemistry currently exists. One promising way to analyze such interfaces is to use in situ ion beam etching, but this requires ion beams able to depth profile both inorganic and organic layers. Mono- or diatomic ion beams commonly used to depth profile inorganic materials usually perform badly on organics, while cluster ion beams perform excellently on organics but yield poor results when organics and inorganics are mixed. Conversely, low energy Cs(+) beams (<500 eV) allow organic and inorganic materials depth profiling with comparable erosion rates. This paper shows a successful depth profiling of a model hybrid system made of metallic (Au, Cr) and organic (tyrosine) layers, sputtered with 500 eV Cs(+) ions. Tyrosine layers capped with metallic overlayers are depth profiled easily, with high intensities for the characteristic molecular ions and other specific fragments. Metallic Au or Cr atoms are recoiled into the organic layer where they cause some damage near the hybrid interface as well as changes in the erosion rate. However, these recoil implanted metallic atoms do not appear to severely degrade the depth profile overall quality. This first successful hybrid depth profiling report opens new possibilities for the study of OLEDs, organic solar cells, or other hybrid devices. PMID:26883532

  9. Hybrid Organic/Inorganic Materials Depth Profiling Using Low Energy Cesium Ions

    NASA Astrophysics Data System (ADS)

    Noël, Céline; Houssiau, Laurent

    2016-05-01

    The structures developed in organic electronics, such as organic light emitting diodes (OLEDs) or organic photovoltaics (OPVs) devices always involve hybrid interfaces, joining metal or oxide layers with organic layers. No satisfactory method to probe these hybrid interfaces physical chemistry currently exists. One promising way to analyze such interfaces is to use in situ ion beam etching, but this requires ion beams able to depth profile both inorganic and organic layers. Mono- or diatomic ion beams commonly used to depth profile inorganic materials usually perform badly on organics, while cluster ion beams perform excellently on organics but yield poor results when organics and inorganics are mixed. Conversely, low energy Cs+ beams (<500 eV) allow organic and inorganic materials depth profiling with comparable erosion rates. This paper shows a successful depth profiling of a model hybrid system made of metallic (Au, Cr) and organic (tyrosine) layers, sputtered with 500 eV Cs+ ions. Tyrosine layers capped with metallic overlayers are depth profiled easily, with high intensities for the characteristic molecular ions and other specific fragments. Metallic Au or Cr atoms are recoiled into the organic layer where they cause some damage near the hybrid interface as well as changes in the erosion rate. However, these recoil implanted metallic atoms do not appear to severely degrade the depth profile overall quality. This first successful hybrid depth profiling report opens new possibilities for the study of OLEDs, organic solar cells, or other hybrid devices.

  10. Simulation of Singlet Exciton Diffusion in Bulk Organic Materials.

    PubMed

    Kranz, Julian J; Elstner, Marcus

    2016-09-13

    We present a scheme for nonadiabatic direct dynamics simulation of Frenkel exciton diffusion in bulk molecular systems. The fluctuations of exciton couplings caused by the molecular motion can crucially influence exciton transport in such materials. This effect can be conveniently taken into account by computing the exciton couplings along molecular dynamics trajectories, as shown recently. In this work, we combine Molecular Dynamics simulations with a Frenkel Hamiltonian into a combined quantum-mechanical/molecular mechanics approach in order to allow for a simultaneous propagation of nuclear and electronic degrees of freedom using nonadiabatic dynamics propagation schemes. To reach the necessary time and length scales, we use classical force-fields and the semiempirical time-dependent density functional tight-binding method in combination with a fragmentation of the electronic structure. Fewest-switches surface-hopping, with adaptions to handle trivial crossings, and the Boltzmann-corrected Ehrenfest method are used to follow the excitonic quantum dynamics according to the classical evolution of the nuclei. As an application, we present the simulation of singlet exciton diffusion in crystalline anthracene, which allows us to address strengths and shortcomings of the presented methodology in detail. PMID:27434173

  11. Abundant Solar Nebula Solids in Comets

    NASA Technical Reports Server (NTRS)

    Messenger, S.; Keller, L. P.; Nakamura-Messenger, K.; Nguyen, A. N.; Clemett, S.

    2016-01-01

    Comets have been proposed to consist of unprocessed interstellar materials together with a variable amount of thermally annealed interstellar grains. Recent studies of cometary solids in the laboratory have shown that comets instead consist of a wide range of materials from across the protoplanetary disk, in addition to a minor complement of interstellar materials. These advances were made possible by the return of direct samples of comet 81P/Wild 2 coma dust by the NASA Stardust mission and recent advances in microscale analytical techniques. Isotopic studies of 'cometary' chondritic porous interplanetary dust particles (CP-IDPs) and comet 81P/Wild 2 Stardust samples show that preserved interstellar materials are more abundant in comets than in any class of meteorite. Identified interstellar materials include sub-micron-sized presolar silicates, oxides, and SiC dust grains and some fraction of the organic material that binds the samples together. Presolar grain abundances reach 1 weight percentage in the most stardust-rich CP-IDPs, 50 times greater than in meteorites. Yet, order of magnitude variations in presolar grain abundances among CP-IDPs suggest cometary solids experienced significant variations in the degree of processing in the solar nebula. Comets contain a surprisingly high abundance of nebular solids formed or altered at high temperatures. Comet 81P/Wild 2 samples include 10-40 micron-sized, refractory Ca- Al-rich inclusion (CAI)-, chondrule-, and ameboid olivine aggregate (AOA)-like materials. The O isotopic compositions of these refractory materials are remarkably similar to their meteoritic counterparts, ranging from 5 percent enrichments in (sup 16) O to near-terrestrial values. Comet 81P/Wild 2 and CP-IDPs also contain abundant Mg-Fe crystalline and amorphous silicates whose O isotopic compositions are also consistent with Solar System origins. Unlike meteorites, that are dominated by locally-produced materials, comets appear to be composed of

  12. The Enigmatic Diffuse Interstellar Bands: A Reservoir of Organic Material

    NASA Astrophysics Data System (ADS)

    McCall, Benjamin

    2008-05-01

    The diffuse interstellar medium of our galaxy contains about 3 billion solar masses of atomic hydrogen, or ˜3x10^66 H atoms. The inventory of identified heavy-atom-containing molecules in diffuse clouds includes CH, CH^+, NH, OH, C2, CN, C2H, and C3H2, and totals to roughly ˜10^59 in number. However, a ubiquitous set of optical absorption lines known as the diffuse interstellar bands (DIBs) belies the likely presence of ˜10^58 large organic molecules that have yet to be identified. The first of the DIBs were observed in 1919, but despite many decades of intensive efforts by laboratory spectroscopists and astronomers the identities of the molecular carriers of the DIBs remain a mystery. After reviewing the history of the DIBs, I will discuss some preliminary results from a large-scale DIBs observing campaign that was conducted on over 119 nights between 1999 and 2003, using the 3.5-meter telescope at the Apache Point Observatory. This survey, undertaken by a collaboration led by Don York at the University of Chicago, has produced high-resolution, high signal-to-noise ratio spectra of over 160 stars, spanning the entire optical region from 3600--10200 å. In particular, I will focus on two ongoing efforts. The first is the generation of a comprehensive spectral atlas of the DIBs based on four heavily reddened sightlines; this atlas will be of great use to spectroscopists who wish to compare their laboratory spectra to interstellar spectra (in hopes of finding a match!). The second is the search for correlations among the different DIBs, and especially the search for sets of DIBs that always have the same relative intensities in different sightlines. Such sets would represent the electronic spectra of individual molecular carriers of the DIBs, and could provide hints about which species should be considered for additional laboratory spectroscopic studies.

  13. Recovery of organic material by supercritical toluene from Turkish Goynuk oil shale

    SciTech Connect

    Yurum, Y.; Karabakan, A. )

    1990-01-01

    The authors describe the effect of the mineral matrix on the recovery of organic material by supercritical toluene extraction from Turkish Goynuk oil shale. Samples were prepared by successive demineralization procedures to study the interaction of different mineral groups during the supercritical interaction. Extraction experiments were done in a stainless steel autoclave of 75 ml capacity at 350{sup 0}C for 60 minutes. Effect of the toluene/kerogen ratio and reaction time on the recovery of organic material was studied.

  14. MOELCULAR SIZE EXCLUSION BY SOIL ORGANIC MATERIALS ESTIMATED FROM THEIR SWELLING IN ORGANIC SOLVENTS

    EPA Science Inventory

    A published method previously developed to measure the swelling characteristics of pow dered coal samples has been adapted for swelling measurements on various peat, pollen, chain, and cellulose samples The swelling of these macromolecular materials is the volumetric manifestatio...

  15. An intuitive thermal-induced surface zwitterionization for versatile, well-controlled haemocompatible organic and inorganic materials.

    PubMed

    Sin, Mei-Chan; Lou, Pei-Tzu; Cho, Chia-He; Chinnathambi, Arunachalam; Alharbi, Sulaiman Ali; Chang, Yung

    2015-03-01

    In this study, a facile and effective strategy is presented for the preparation of a series of zwitterionic poly(sulfobetaine methacrylate) (pSBMA)-grafted organic and inorganic biomaterials with well-controlled haemocompatibility via intuitive thermal-induced graft polymerization. The research focused on the effects of zwitterionic surface packing density on human blood compatibility by varying the SBMA monomer concentration on the silanized silicon wafer substrates. A 0.2 M SBMA monomer solution was found to not only produce Si wafer surfaces with ideal zwitterionic surface packing density and uniform, evenly distributed pSBMA grafting coverage but also yield optimal hydrophilicity and haemocompatibility. SBMA monomer concentrations lower and greater than 0.2 M yielded a zwitterionic surface with low grafting coverage. This study also demonstrated that the same, intuitive thermal-induced graft polymerization strategy could be applied to a variety of organic polymeric, inorganic ceramic and metal oxide biomaterials to improve haemocompatibility. Among the tested organic and inorganic materials, however, it was found that inorganic biomaterials demonstrated greater resistance to protein and platelet adhesions. It was hypothesized that the ozone treatment, which generated an abundance of hydroxide groups on inorganic substrate interfaces, might have given the inorganic biomaterials a more stable silanized layer yielding a preferable reaction state and resulted in sturdier and more durable pSBMA grafting. PMID:25638723

  16. Methods for associating or dissociating guest materials with a metal organic framework, systems for associating or dissociating guest materials within a series of metal organic frameworks, thermal energy transfer assemblies, and methods for transferring thermal energy

    DOEpatents

    McGrail, B. Peter; Brown, Daryl R.; Thallapally, Praveen K.

    2016-08-02

    Methods for releasing associated guest materials from a metal organic framework are provided. Methods for associating guest materials with a metal organic framework are also provided. Methods are provided for selectively associating or dissociating guest materials with a metal organic framework. Systems for associating or dissociating guest materials within a series of metal organic frameworks are provided. Thermal energy transfer assemblies are provided. Methods for transferring thermal energy are also provided.

  17. Methods for associating or dissociating guest materials with a metal organic framework, systems for associating or dissociating guest materials within a series of metal organic frameworks, thermal energy transfer assemblies, and methods for transferring thermal energy

    DOEpatents

    McGrail, B. Peter; Brown, Daryl R.; Thallapally, Praveen K.

    2014-08-05

    Methods for releasing associated guest materials from a metal organic framework are provided. Methods for associating guest materials with a metal organic framework are also provided. Methods are provided for selectively associating or dissociating guest materials with a metal organic framework. Systems for associating or dissociating guest materials within a series of metal organic frameworks are provided. Thermal energy transfer assemblies are provided. Methods for transferring thermal energy are also provided.

  18. Thermal storage in drywall using organic phase-change material

    SciTech Connect

    Shapiro, M.M.; Feldman, D.; Hawes, D.; Banu, D.

    1987-01-01

    Two mixtures of phase-change material (PCM), 49% butyl stearate with 48% butyl palmitate, and 55% lauric acid with 45% capric acid, diluted 10% with fire retardant, were diffused into 13-mm (0.5-in.) wallboard. No exudation of liquid PCM occurs below 25% by weight. In the wallboard, initial PCM freezing points were 21/sup 0/ and 22/sup 0/C (70/sup 0/ and 72/sup 0/F), respectively, with melting points of 17/sup 0/ and 18/sup 0/C (63/sup 0/ and 64/sup 0/F). For a 4/sup 0/C (7/sup 0/F) temperature swing, thermal storage capacities up to 350 kJ/m/sup 2/ (31 Btu/ft/sup 2/) and 317 kJ/m/sup 2/ (28 Btu/ft/sup 2/), respectively, are available. These are equivalent to about 3.8 cm (1.5 in.) of concrete cycled through 7/sup 0/C (13/sup 0/F). Preliminary tests showed little extra flame spread beyond that of unloaded wallboard. The thermal conductivity of the wallboard increased from 0.19 to 0.22 W/m /sup 0/C (0.11 to 0.13 Btu/h ft /sup 0/F) with liquid PCM. During melting, the effective thermal diffusivity falls from 2.1 x 10/sup -7/ m/sup 2//s (2.3 x 10/sup -6/ ft/sup 2//s) for the unloaded wallboard to 1.4 x 10/sup -7/ m/sup 2//s (1.5 x 10/sup -6/ ft/sup 2//s) with 23.4% butyl stearate-palmitate and to 1.6 x 10/sup -7/ m/sup 2//s (1.7 x 10/sup -6/ ft/sup 2//s) with 28% of the lauric-capric mixture. (The mixture fraction is defined as the ratio of PCM mass to gypsum mass.)

  19. Organic Materials in the Undergraduate Laboratory: Microscale Synthesis and Investigation of a Donor-Acceptor Molecule

    ERIC Educational Resources Information Center

    Pappenfus, Ted M.; Schliep, Karl B.; Dissanayake, Anudaththa; Ludden, Trevor; Nieto-Ortega, Belen; Lopez Navarrete, Juan T.; Ruiz Delgado, M. Carmen; Casado, Juan

    2012-01-01

    A series of experiments for undergraduate courses (e.g., organic, physical) have been developed in the area of small molecule organic materials. These experiments focus on understanding the electronic and redox properties of a donor-acceptor molecule that is prepared in a convenient one-step microscale reaction. The resulting intensely colored…

  20. Method of loading organic materials with group III plus lanthanide and actinide elements

    DOEpatents

    Bell, Zane W.; Huei-Ho, Chuen; Brown, Gilbert M.; Hurlbut, Charles

    2003-04-08

    Disclosed is a composition of matter comprising a tributyl phosphate complex of a group 3, lanthanide, actinide, or group 13 salt in an organic carrier and a method of making the complex. These materials are suitable for use in solid or liquid organic scintillators, as in x-ray absorption standards, x-ray fluorescence standards, and neutron detector calibration standards.

  1. Lithium-Ion-Battery Anode Materials with Improved Capacity from a Metal-Organic Framework.

    PubMed

    Lin, Xiao-Ming; Niu, Ji-Liang; Lin, Jia; Wei, Lei-Ming; Hu, Lei; Zhang, Gang; Cai, Yue-Peng

    2016-09-01

    We present a porous metal-organic framework (MOF) with remarkable thermal stability that exhibits a discharge capacity of 300 mAh g(-1) as an anode material for a lithium-ion battery. Pyrolysis of the obtained MOF gives an anode material with improved capacity (741 mAh g(-1)) and superior cyclic stability. PMID:27548622

  2. Organizing and Planning. Developing Publication Materials. Student Manual and Instructor's Manual.

    ERIC Educational Resources Information Center

    Chapman, Pat

    Supporting performance objective 3 of the V-TECS (Vocational-Technical Education Consortium of States) Secretarial Catalog, both a set of student materials and an instructor's manual on developing publication materials are included in this packet. (The packet is the second in a set of three on organizing and planning--CE 016 987-989.) The student…

  3. An Annotated Bibliography of Materials Designed and Organized for Adult Use in Discussion Groups.

    ERIC Educational Resources Information Center

    Ellison, John W.

    This first annotated bibliography of materials designed and organized for adult use in disucssion groups includes both book and nonbook material. Areas dealt with are: art, censorship, change, child guidance, communication, crime, democracy, economics, education, evolution, food, foreign affairs, forgetting, generation gap, gold, good and evil,…

  4. Factors Affecting the Battery Performance of Anthraquinone-based Organic Cathode Materials

    SciTech Connect

    Xu, Wu; Read, Adam L.; Koech, Phillip K.; Hu, Dehong; Wang, Chong M.; Xiao, Jie; Padmaperuma, Asanga B.; Graff, Gordon L.; Liu, Jun; Zhang, Jiguang

    2012-02-01

    Two organic cathode materials based on poly(anthraquinonyl sulfide) structure with different substitution positions were synthesized and their electrochemical behavior and battery performances were investigated. The substitution positions on the anthraquinone structure, binders for electrode preparation and electrolyte formulations have been found to have significant effects on the battery performances of such organic cathode materials. The substitution position with less steric stress has higher capacity, longer cycle life and better high-rate capability. Polyvinylidene fluoride binder and ether-based electrolytes are favorable for the high capacity and long cycle life of the quinonyl organic cathodes.

  5. Field-verification program (aquatic disposal): comparison of field and laboratory bioaccumulation of organic and inorganic contaminants from Black Rock Harbor dredged material. Final report

    SciTech Connect

    Lake, J.L.; Galloway, W.; Hoffman, G.; Nelson, W.; Scott, K.J.

    1988-05-01

    The utility of laboratory tests for predicting bioaccumulation of contaminants in the field was evaluated by comparing the identities, relative abundances, and quantities of organic and inorganic contaminants accumulated by organisms exposed to dredged material in both laboratory and field studies. The organisms used were Mytilus edulis (a filter-feeding bivalve) and Nephtys incisa (a benthic polychaete). These organisms were exposed in the laboratory and in the field to a contaminated dredged material from Black Rock Harbor (BRH), Connecticut. Both organisms had positive and negative attributes for these exposure studies. Mytilus edulis appeared to reach steady-state in laboratory-exposure studies. However, the determination of field-exposure concentrations was precluded due to limitations on obtaining an integrated water sample during the exposure period in the field. Nephtys incisa did not appear to reach steady-state in laboratory studies and, although field-exposure data (sediment concentrations) were obtained, the exposure zone for these organisms could not be determined. Estimates of field exposures were made using laboratory-derived exposure-residue relationships and residues from field-exposed organisms. These field-exposure estimates were compared with those estimated using exposure data from the field. A comparison of these estimates showed the same general trends in the exposure-residue relationships from the laboratory and the field and further supports the laboratory predictive approach.

  6. Apparatus for measuring the Seebeck coefficients of highly resistive organic semiconducting materials

    NASA Astrophysics Data System (ADS)

    Cai, H. Y.; Cui, D. F.; Li, Y. T.; Chen, X.; Zhang, L. L.; Sun, J. H.

    2013-04-01

    A Seebeck coefficient measurement apparatus for high resistance organic semiconductor materials has been designed and built. It can measure materials with resistance over 7 × 1012 Ω. This is the highest material resistance value ever reported for Seebeck coefficient measurement. A cyclic temperature gradient generation technique and a corresponding algorithm are proposed to eliminate the negative effects of the long term drift of Seebeck voltage. Sources of errors in these measurements are discussed.

  7. Electrical, optical, and magnetic properties of organic solid-state materials IV. Materials Research Society, symposium proceedings Volume 488

    SciTech Connect

    Reynolds, J.R.; Jen, A.K.Y.; Rubner, M.F.; Chiang, L.Y.; Dalton, L.R.

    1998-07-01

    The symposium, Electrical, Optical, and Magnetic Properties of Organic Solid-State Materials IV, was sponsored by the Materials Research Society and held December 1--5, 1997, in Boston, Massachusetts. Early studies of charge transport in conducting polymers have evolved from the elucidation of fundamental structure/function relationships to applications as batteries, simple electrical devices such as diodes, chemical sensors, antistatic coatings, microwave and millimeter wave-absorbing materials, and photochromic devices. A particularly exciting evolution has been the discovery and development of organic light-emitting diodes (OLEDs) which appear to be nearing commercialization in an amazingly short period of time. This application is of particular interest because both electrical and optical properties must be considered, and these have been important parallel themes of the conference. Moreover, nanostructure control is important for OLEDs, and nanoscale architectural engineering has been an increasingly important theme of the conference. Indeed, not only has the study of conjugated (quasidelocalized) electrons in organic solid-state materials resulted in interesting physical properties and device applications, but the desire to exploit these properties has promoted the development of new synthesis and processing methodologies to achieve special nanoscale and microscale structures. One hundred five papers have been processed separately for inclusion on the data base.

  8. Capacitance measurements to directly investigate exciton behaviors in organic photovoltaic materials

    NASA Astrophysics Data System (ADS)

    Yu, Haomiao; Yi, Ruichen; Li, Wenbin; Zhang, Jiawei; He, Yun; Zeng, Qi; Hou, Xiaoyuan

    2015-11-01

    The major obstacle to directly determining exciton behaviors in common organic photovoltaic materials (e.g. fullerene) is the absence of room-temperature luminescence. Regarding this issue, the capacitance dependences on incident light intensity and electric field are investigated for several typical organic photovoltaic materials. Distinctive correlations between capacitance and light intensity/electric field are observed for different samples. Moreover, the exciton dissociation probability of fullerene and the charge density of pentacene are extracted from the capacitance-voltage (C-V) characteristics. All these results demonstrate a straight pathway to survey exciton behaviors in those materials with almost no luminescence at room temperature.

  9. Material organizations in the 1994 Addenda ASME Code Section III, Division I

    SciTech Connect

    Bressler, M.N.; Kist, N.C.

    1995-12-01

    This paper provides a history of the requirements for materials in ASME Code Section 3, Nuclear Power Plant Components, from its inception to the present 1992 Edition and the new 1994 Addenda. Major events in the development of the Code are listed, and the organizations involved in materials that are covered by this standard arc described. Changes to duties and responsibilities of individuals and organizations performing Section 3 material activities are identified, and the requirements for accreditation and qualification are discussed. A Code Case to provide alternatives to compliance is presented.

  10. Bridged polysilsesquioxane xerogels: A molecular based approach for the preparation of porous hybrid organic-inorganic materials

    SciTech Connect

    Small, J.H.; Shea, K.J.; Loy, D.A.

    1995-06-01

    Bridged polysilsesquioxanes represent an interesting family of hybrid organic-inorganic composite materials. It has been shown that manipulation of the organic bridging component offers the potential for the synthesis of a variety of materials with a range of surface areas and porosities. In addition, incorporation of a heteroatom within the bridging organic component allows for further chemical transformation of the polysilsesquioxane material.

  11. Heterogeneous Chemical Transformation of Incident Exogenous Organic Material in Earth's Upper Atmosphere

    NASA Astrophysics Data System (ADS)

    Belle, C. L.; Kress, M. E.; Iraci, L. T.

    2009-12-01

    On average, 10^8 g of solar system debris impinges on the Earth system each day. It is estimated that a few percent of this material is carbonaceous in nature, yet the fate of this organic material once it enters our atmosphere is unexplored. Much of this incoming material arrives in the form of micrometeoroids which are large enough to suffer drag heating and volatilize their organic material. Preliminary work shows that the organic material contained in particles with diameters on the order of 10-100 um is expected to be volatilized at altitudes of 100-120 km. Observed species include aromatic compounds such as alkybenzenes, phenol, benzonitrile, naphthalene, and styrene. Once liberated, these molecules may be transformed by processes at the boundary of space, or may survive to be mixed throughout the atmosphere. Sulfuric acid particles exist in Earth's upper atmosphere, and organic compounds often react strongly with this acid. We will report the results of laboratory and theoretical investigations of the interaction of aromatic compounds with surrogate matrices which mimic upper atmospheric particles. These studies will explore how exogenous organic compounds are altered after liberation at altitudes near 100 km and will determine if they survive to reach the surface of the Earth, where they may have provided the starting materials for the evolution of life on Earth or on other bodies.

  12. Method for monitoring the crystallization of an organic material from a liquid

    DOEpatents

    Asay, Blaine W.; Henson, Bryan F.; Sander, Robert K.; Robinson, Jeanne M.; Son, Steven F.; Dickson, Peter M.

    2004-10-05

    Method for monitoring the crystallization of at least one organic material from a liquid. According to the method, a liquid having at least one organic material capable of existing in at least one non-centrosymmetric phase is prepared. The liquid is interrogated with a laser beam at a chosen wavelength. As at least a portion of the at least one organic material crystallizes from the liquid, the intensity of any light scattered by the crystallized material at a wavelength equal to one-half the chosen wavelength of the interrogating laser beam is monitored. If the intensity of this scattered light, increases, then the crystals that form include at least one non-cetrosymmetric phase.

  13. Humic and fluvic acids and organic colloidal materials in the environment

    SciTech Connect

    Gaffney, J.S.; Marley, N.A.; Clark, S.B.

    1996-04-01

    Humic substances are ubiquitous in the environment, occurring in all soils, waters, and sediments of the ecosphere. Humic substances arise from the decomposition of plant and animal tissues yet are more stable than their precursors. Their size, molecular weight, elemental composition, structure, and the number and position of functional groups vary, depending on the origin and age of the material. Humic and fulvic substances have been studied extensively for more than 200 years; however, much remains unknown regarding their structure and properties. Humic substances are those organic compounds found in the environment that cannot be classified as any other chemical class of compounds. They are traditionally defined according to their solubilities. Fulvic acids are those organic materials that are soluble in water at all pH values. Humic acids are those materials that are insoluble at acidic pH values (pH < 2) but are soluble at higher pH values. Humin is the fraction of natural organic materials that is insoluble in water at all pH values. These definitions reflect the traditional methods for separating the different fractions from the original mixture. The humic content of soils varies from 0 to almost 10%. In surface waters, the humic content, expressed as dissolved organic carbon (DOC), varies from 0.1 to 50 ppm in dark-water swamps. In ocean waters, the DOC varies from 0.5 to 1.2 ppm at the surface, and the DOC in samples from deep groundwaters varies from 0.1 to 10 ppm. In addition, about 10% of the DOC in surface waters is found in suspended matter, either as organic or organically coated inorganic particulates. Humic materials function as surfactants, with the ability to bind both hydrophobic and hydrophyllic materials, making numic and fluvic materials effective agents in transporting both organic and inorganic contaminants in the environment.

  14. A homochiral metal-organic porous material for enantioselective separation and catalysis

    NASA Astrophysics Data System (ADS)

    Seo, Jung Soo; Whang, Dongmok; Lee, Hyoyoung; Jun, Sung Im; Oh, Jinho; Jeon, Young Jin; Kim, Kimoon

    2000-04-01

    Inorganic zeolites are used for many practical applications that exploit the microporosity intrinsic to their crystal structures. Organic analogues, which are assembled from modular organic building blocks linked through non-covalent interactions, are of interest for similar applications. These range from catalysis, separation and sensor technology to optoelectronics, with enantioselective separation and catalysis being especially important for the chemical and pharmaceutical industries. The modular construction of these analogues allows flexible and rational design, as both the architecture and chemical functionality of the micropores can, in principle, be precisely controlled. Porous organic solids with large voids and high framework stability have been produced, and investigations into the range of accessible pore functionalities have been initiated. For example, catalytically active organic zeolite analogues are known, as are chiral metal-organic open-framework materials. However, the latter are only available as racemic mixtures, or lack the degree of framework stability or void space that is required for practical applications. Here we report the synthesis of a homochiral metal-organic porous material that allows the enantioselective inclusion of metal complexes in its pores and catalyses a transesterification reaction in an enantioselective manner. Our synthesis strategy, which uses enantiopure metal-organic clusters as secondary building blocks, should be readily applicable to chemically modified cluster components and thus provide access to a wide range of porous organic materials suitable for enantioselective separation and catalysis.

  15. Hydrogen-Bonded Organic Frameworks (HOFs): A New Class of Porous Crystalline Proton-Conducting Materials.

    PubMed

    Karmakar, Avishek; Illathvalappil, Rajith; Anothumakkool, Bihag; Sen, Arunabha; Samanta, Partha; Desai, Aamod V; Kurungot, Sreekumar; Ghosh, Sujit K

    2016-08-26

    Two porous hydrogen-bonded organic frameworks (HOFs) based on arene sulfonates and guanidinium ions are reported. As a result of the presence of ionic backbones appended with protonic source, the compounds exhibit ultra-high proton conduction values (σ) 0.75× 10(-2)  S cm(-1) and 1.8×10(-2)  S cm(-1) under humidified conditions. Also, they have very low activation energy values and the highest proton conductivity at ambient conditions (low humidity and at moderate temperature) among porous crystalline materials, such as metal-organic frameworks (MOFs) and covalent organic frameworks (COFs). These values are not only comparable to the conventionally used proton exchange membranes, such as Nafion used in fuel cell technologies, but is also the highest value reported in organic-based porous architectures. Notably, this report inaugurates the usage of crystalline hydrogen-bonded porous organic frameworks as solid-state proton conducting materials. PMID:27464784

  16. A Comparison of Dissolved and Particulate Organic Material in Two Southwestern Desert River Systems

    NASA Astrophysics Data System (ADS)

    Haas, P. A.; Brooks, P.

    2001-12-01

    Desert river systems of the southwestern U.S. acquire a substantial fraction of their dissolved organic matter (DOM) from the terrestrial environment during episodic rain events. This DOM provides carbon for stream metabolism and nitrogen, which is limiting in lower order streams in this environment. The San Pedro and Rio Grande Rivers represent two endpoints of catchment scale, discharge, and land use in the southwest. The San Pedro is a protected riparian corridor (San Pedro Riparian National Conservation Area), while the middle Rio Grande is a large river with extensive agriculture, irrigation, and reservoirs. Relative abundance and spectral properties of fulvic acids isolated from filtered samples were used to determine the source of dissolved organic carbon (DOC). Total DOC and particulate organic carbon (POC) changes with respect to episodic flooding events were compared for the two river systems. The San Pedro River DOC concentrations remain low approximately 2.2 to 3.3 ppm unless a relatively large storm event occurs when concentrations may go above 5.5 ppm (1000cfs flow). In contrast typical concentrations for the Rio Grande were approximately 5 ppm during the monsoon season. Particulate organic matter (POM) appears to be a more significant source of organic matter to the San Pedro than DOM. The relative importance of terrestrial vs. aquatic and dissolved vs. particulate organic matter with respect to aquatic ecosystems will be discussed.

  17. A material sensitivity study on the accuracy of deformable organ registration using linear biomechanical models

    SciTech Connect

    Chi, Y.; Liang, J.; Yan, D.

    2006-02-15

    Model-based deformable organ registration techniques using the finite element method (FEM) have recently been investigated intensively and applied to image-guided adaptive radiotherapy (IGART). These techniques assume that human organs are linearly elastic material, and their mechanical properties are predetermined. Unfortunately, the accurate measurement of the tissue material properties is challenging and the properties usually vary between patients. A common issue is therefore the achievable accuracy of the calculation due to the limited access to tissue elastic material constants. In this study, we performed a systematic investigation on this subject based on tissue biomechanics and computer simulations to establish the relationships between achievable registration accuracy and tissue mechanical and organ geometrical properties. Primarily we focused on image registration for three organs: rectal wall, bladder wall, and prostate. The tissue anisotropy due to orientation preference in tissue fiber alignment is captured by using an orthotropic or a transversely isotropic elastic model. First we developed biomechanical models for the rectal wall, bladder wall, and prostate using simplified geometries and investigated the effect of varying material parameters on the resulting organ deformation. Then computer models based on patient image data were constructed, and image registrations were performed. The sensitivity of registration errors was studied by perturbating the tissue material properties from their mean values while fixing the boundary conditions. The simulation results demonstrated that registration error for a subvolume increases as its distance from the boundary increases. Also, a variable associated with material stability was found to be a dominant factor in registration accuracy in the context of material uncertainty. For hollow thin organs such as rectal walls and bladder walls, the registration errors are limited. Given 30% in material uncertainty

  18. Interactions between organisms and parent materials of a constructed Technosol shape its hydrostructural properties

    NASA Astrophysics Data System (ADS)

    Deeb, Maha; Grimaldi, Michel; Lerch, Thomas Z.; Pando, Anne; Gigon, Agnès; Blouin, Manuel

    2016-04-01

    There is no information on how organisms influence hydrostructural properties of constructed Technosols and how such influence will be affected by the parent-material composition factor. In a laboratory experiment, parent materials, which were excavated deep horizons of soils and green waste compost (GWC), were mixed at six levels of GWC (from 0 to 50 %). Each mixture was set up in the presence/absence of plants and/or earthworms, in a full factorial design (n = 96). After 21 weeks, hydrostructural properties of constructed Technosols were characterized by soil shrinkage curves. Organisms explained the variance of hydrostructural characteristics (19 %) a little better than parent-material composition (14 %). The interaction between the effects of organisms and parent-material composition explained the variance far better (39 %) than each single factor. To summarize, compost and plants played a positive role in increasing available water in macropores and micropores; plants were extending the positive effect of compost up to 40 and 50 % GWC. Earthworms affected the void ratio for mixtures from 0 to 30 % GWC and available water in micropores, but not in macropores. Earthworms also acted synergistically with plants by increasing their root biomass, resulting in positive effects on available water in macropores. Organisms and their interaction with parent materials positively affected the hydrostructural properties of constructed Technosols, with potential positive consequences on resistance to drought or compaction. Considering organisms when creating Technosols could be a promising approach to improve their fertility.

  19. Temperature response of litter and soil organic matter decomposition is determined by chemical composition of organic material.

    PubMed

    Erhagen, Björn; Öquist, Mats; Sparrman, Tobias; Haei, Mahsa; Ilstedt, Ulrik; Hedenström, Mattias; Schleucher, Jürgen; Nilsson, Mats B

    2013-12-01

    The global soil carbon pool is approximately three times larger than the contemporary atmospheric pool, therefore even minor changes to its integrity may have major implications for atmospheric CO2 concentrations. While theory predicts that the chemical composition of organic matter should constitute a master control on the temperature response of its decomposition, this relationship has not yet been fully demonstrated. We used laboratory incubations of forest soil organic matter (SOM) and fresh litter material together with NMR spectroscopy to make this connection between organic chemical composition and temperature sensitivity of decomposition. Temperature response of decomposition in both fresh litter and SOM was directly related to the chemical composition of the constituent organic matter, explaining 90% and 70% of the variance in Q10 in litter and SOM, respectively. The Q10 of litter decreased with increasing proportions of aromatic and O-aromatic compounds, and increased with increased contents of alkyl- and O-alkyl carbons. In contrast, in SOM, decomposition was affected only by carbonyl compounds. To reveal why a certain group of organic chemical compounds affected the temperature sensitivity of organic matter decomposition in litter and SOM, a more detailed characterization of the (13) C aromatic region using Heteronuclear Single Quantum Coherence (HSQC) was conducted. The results revealed considerable differences in the aromatic region between litter and SOM. This suggests that the correlation between chemical composition of organic matter and the temperature response of decomposition differed between litter and SOM. The temperature response of soil decomposition processes can thus be described by the chemical composition of its constituent organic matter, this paves the way for improved ecosystem modeling of biosphere feedbacks under a changing climate. PMID:23907960

  20. Size-controlled hydroxyapatite nanoparticles as self-organized organic-inorganic composite materials.

    PubMed

    Rusu, Viorel Marin; Ng, Chuen-How; Wilke, Max; Tiersch, Brigitte; Fratzl, Peter; Peter, Martin G

    2005-09-01

    This paper presents some results concerning the size-controlled hydroxyapatite nanoparticles obtained in aqueous media in a biopolymer matrix from soluble precursors salts. Taking the inspiration from nature, where composite materials made of a polymer matrix and inorganic fillers are often found, e.g. bone, shell of crustaceans, shell of eggs, etc., the feasibility on making composite materials containing chitosan and nanosized hydroxyapatite was investigated. A stepwise co-precipitation approach was used to obtain different types of composites by means of different ratio between components. The synthesis of hydroxyapatite was carried out in the chitosan matrix from calcium chloride and sodium dihydrogenphosphate in alkaline solutions at moderate pH of 10-11 for 24 h. Our research is focused on studying and understanding the structure of this class of composites, aiming at the development of novel materials, controlled at the nanolevel scale. The X-ray diffraction technique was employed in order to study the kinetic of hydroxyapatite formation in the chitosan matrix as well as to determine the HAp crystallite sizes in the composite samples. The hydroxyapatite synthesized using this route was found to be nano-sized (15-50 nm). Moreover, applying an original approach to analyze the (002) XRD diffraction peak profile of hydroxyapatite by using a sum of two Gauss functions, the bimodal distribution of nanosized hydroxyapatite within the chitosan matrix was revealed. Two types of size distribution domains such as cluster-like (between 200 and 400 nm), which are the habitat of ''small'' hydroxyapatite nanocrystallites and scattered-like, which are the habitat of ''large'' hydroxyapatite nanocrystallites was probed by TEM and CSLM. The structural features of composites suggest that self-assembly processes might be involved. The composites contain nanosized hydroxyapatite with structural features close to those of biological apatites that make them attractive for bone

  1. Complex Organic Materials on Planetary Satellites and Other Small Bodies of the Solar System

    NASA Technical Reports Server (NTRS)

    Cruikshank, Dale P.

    2006-01-01

    The search for organic materials on small bodies of the Solar System is conducted spectroscopically from Earth-based telescopes and from spacecraft. Although the carbonaceous meteorites carry a significant inventory of complex organic solids, the sources of these meteorites have not been identified. Infrared spectra of a sample of the suspected sources, the C- and D-class asteroids, including new data from the Spitzer Space Telescope, show signatures of silicates, but none diagnostic of organic compounds. In the absence of discrete spectral features, the low albedos and colors in the visible and near-IR spectral regions are the principal links between the organic-bearing meteorites and the asteroids. While Pluto and a few trans-neptunian objects show spectral signatures of frozen CH4. Solid CH3OH has been identified on two Centaur objects in the outer Solar System. In some cases the red colors of those objects suggest the presence of tholins. The VIMS instrument aboard the Cassini spacecraft in orbit around Saturn has detected near-IR spectral features on at least three of Saturn's satellites that are indicative or suggestive of organic molecules. One entire hemisphere of the satellite Iapetus is covered with low-albedo material that shows a spectral signature of aromatic hydrocarbons (3.3 microns) and the -CH2 stretching mode bands of an aliphatic component. Organics absorbing at 3.44 microns are suspected in the region of the south pole of Enceladus, and also on the surface of Phoebe. Organic material may originate on icy bodies in the current epoch by various processes of energy deposition into native material, or they may fall to the surface from an external (probably cometary) source. Some organic material may be pre-solar, having originated in the interstellar medium before the formation of the Solar System. Using the techniques of remote sensing, its detection and analysis are slow and difficult.

  2. The Impact and Oxidation Survival of Selected Meteoritic Compounds: Signatures of Asteroid Organic Material on Planetary Surfaces

    NASA Technical Reports Server (NTRS)

    Cooper, George; Horz, Fred; Oleary, Alanna; Chang, Sherwood

    2013-01-01

    Polar, non-volatile organic compounds may be present on the surfaces (or near surfaces) of multiple Solar System bodies. If found, by current or future missions, it would be desirable to determine the origin(s) of such compounds, e.g., asteroidal or in situ. To test the possible survival of meteoritic compounds both during impacts with planetary surfaces and under subsequent (possibly) harsh ambient conditions, we subjected known meteoritic compounds to relatively high impact-shock pressures and/or to varying oxidizing/corrosive conditions. Tested compounds include sulfonic and phosphonic acids (S&P), polyaromatic hydrocarbons (PAHs) amino acids, keto acids, dicarboxylic acids, deoxy sugar acids, and hydroxy tricarboxylic acids (Table 1). Meteoritic sulfonic acids were found to be relatively abundant in the Murchison meteorite and to possess unusual S-33 isotope anomalies (non mass-dependent isotope fractionations). Combined with distinctive C-S and C-P bonds, the S&P are potential signatures of asteroidal organic material.

  3. Recent advances in porous polyoxometalate-based metal-organic framework materials.

    PubMed

    Du, Dong-Ying; Qin, Jun-Sheng; Li, Shun-Li; Su, Zhong-Min; Lan, Ya-Qian

    2014-07-01

    Polyoxometalate (POM)-based metal-organic framework (MOF) materials contain POM units and generally generate MOF materials with open networks. POM-based MOF materials, which utilize the advantages of both POMs and MOFs, have received increasing attention, and much effort has been devoted to their preparation and relevant applications over the past few decades. They have good prospects in catalysis owing to the electronic and physical properties of POMs that are tunable by varying constituent elements. In this review, we present recent developments in porous POM-based MOF materials, including their classification, synthesis strategies, and applications, especially in the field of catalysis. PMID:24676127

  4. Estimated temperatures of organic materials in the TMI-2 reactor building during hydrogen burn

    SciTech Connect

    Schutz, H.W.; Nagata, P.K.

    1982-12-01

    Maximum surface temperatures attained by certain materials during the hydrogen burn associated with the March 1979 accident at TMI-2 are estimated, using photographs and material samples from the reactor building. Thermal degradation, melting, and charring noted in the photographs, and the chemical and thermal analyses of polymeric and organic materials indicated an increase in temperature with elevation in the reactor building. The maximum material surface temperatures estimated ranged from 360 to 500/sup 0/F (455 to 533/sup 0/K). Analyses were performed to estimate the damage to electrical cables and insulation. Based on temperatures reached and approximate duration, greater than 90% of cable insulation life remains.

  5. Microbial population in the biomass adhering to supporting material in a packed-bed reactor degrading organic solid waste.

    PubMed

    Sasaki, Kengo; Haruta, Shin; Ueno, Yoshiyuki; Ishii, Masaharu; Igarashi, Yasuo

    2007-06-01

    An anaerobic packed-bed reactor using carbon fiber textiles (CFT) as the supporting material was continuously operated using an artificial garbage slurry. 16S rRNA gene analysis showed that many bacteria in the biomass adhering to CFT were closely related to those observed from other anaerobic environments, although a wide variety of unidentified bacteria were also found. Dot blot hybridization results clarified that 16S rRNA levels of methanogens in the adhering biomass were higher than those in the effluent. Based on microscopic observation, the adhering biomass consisted of microorganisms, organic material, and void areas. Bacteria and Archaea detected by fluorescence in situ hybridization were distributed from the surface to the inner regions of the adhering biomass. Methanosarcina sp. tended to be more abundant in the inner part of the adhering biomass than at the surface. This is the first report to elucidate the structure of the microbial community on CFT in a packed-bed reactor. PMID:17334757

  6. Response of Organic Materials to Hypervelocity Impacts (up to 11.2 km/sec)

    NASA Astrophysics Data System (ADS)

    Bass, D. S.; Murphy, W. M.; Miller, G. P.; Grosch, D. J.; Walker, J. D.; Mullin, A.; Waite, J. H.

    1998-09-01

    It is speculated that organic-rich planetesimals played a role in the origin of life on Earth. However, the mechanism by which organics could have been delivered from space to a planetary surface is difficult to determine. Particularly problematic is the question of the stability of organic material under hypervelocity impact conditions. Although some evidence suggests organic molecules cannot survive impacts from projectile velocities greater than about 10 km/sec [1], other investigators have found that impacts create a favorable environment for post-shock recombination of organic molecules in the plume phase [2, 3]. Understanding the mechanisms involved in delivering organics to a planetary surface remains difficult to assess due to the lack of experimental results of hypervelocity impacts, particularly in the velocity range of tens of km/sec. Organic material preservation and destruction from impact shocks, the synthesis of organics in the post-impact plume environment, and implications of these processes for Earth and Mars can be investigated by launching an inorganic projectile into an analog planetesimal-and-bolide organic-rich target. We explored the pressure and temperature ranges of hypervelocity impacts (11.2 km/sec) through simulations with CTH impact physics computer code. Using an inhibited shaped-charge launcher, we also experimentally determined the response of organic material to hypervelocity impacts. Initial work focused on saturating well-characterized zeolitic tuff with an aqueous solution containing dissolved naphthalene, a common polycyclic aromatic hydrocarbon (PAH). Porosity measurements, thin section, and x-ray diffraction analyses were performed to determine that the tuff is primarily fine-grained clinoptilolite. In order to distinguish between contaminants and compounds generated or destroyed in the impact, we tagged the aqueous component of our target with deuterium. Experimental tests revealed that to first order, naphthalene survived

  7. Relating desorption of polycyclic aromatic hydrocarbons from harbour sludges to type of organic material

    NASA Astrophysics Data System (ADS)

    Heister, K.; Pols, S.; Loch, J. P. G.; Bosma, T.

    2009-04-01

    For decades, polycyclic aromatic hydrocarbons (PAH) cause great concern as environmental pollutants. Especially river and marine harbour sediments are frequently polluted with PAH derived from surface runoff, fuel and oil spills due to shipping and industrial activities, industrial waste and atmospheric deposition. Harbour sediments contain large amounts of organic carbon and clay minerals and are therefore not easy to remediate and have to be stored in sludge depositories after dredging to maintain sufficient water depth for shipping. The organic contaminants will be adsorbed to particles, leached in association with dissolved organic material or microbially degraded. However, compounds of high molecular weight are very persistent, particularly under anaerobic conditions, thus giving rise to the potential to become desorbed again. PAH adsorb mainly to organic material. It has been shown that components of the organic material with a low polarity and a high hydrophobicity like aliphatic and aromatic components exhibit a high sorption capacity for hydrophobic organic contaminants like PAH. Accordingly, not only the amount but also the type of organic material needs to be determined in order to be able to predict contaminant behaviour. In this study, desorption behaviour of the 16 EPA-PAH in two different harbour sludges from the port of Rotterdam, the Netherlands, has been investigated. The Beerkanaal (BK) site is located relatively close to the North Sea and represents a brackish environment; the Beneden Merwede River (BMR) site originates from a fresh water environment and is close to industrial sites. The samples were placed in dialysis membranes and brought into contact with water for a period of 130 days. At several time intervals, water samples were retrieved for analysis of pH, dissolved organic carbon (DOC) content, electrical conductivity and PAH concentrations. The experiment was conducted at 4 and at 20°C. Although the samples were initially treated with

  8. Fibrin structure in organized thrombotic material removed during pulmonary artery endarterectormy: the effect of vessel calibre.

    PubMed

    Mazur, Piotr; Gawęda, Bogusław; Natorska, Joanna; Ząbczyk, Michał; Undas, Anetta; Sadowski, Jerzy; Kopeć, Grzegorz; Waligóra, Marcin; Podolec, Piotr; Kapelak, Bogusław

    2016-08-01

    Pulmonary endarterectomy (PEA) is a curative therapeutic approach in patients with chronic thromboembolic pulmonary hypertension (CTEPH). The location-dependent structural differences of thrombotic material found in pulmonary arteries in CTEPH are poorly investigated. We present the case of a 47-year-old woman with antiphospholipid syndrome, diabetes mellitus and abnormal fibrin phenotype, who underwent PEA for CTEPH. Intravascular material removed bilaterally during PEA (from lobar, segmental and sub-segmental arteries) has been studied using light and scanning electron microscopy (SEM). Light microscopy showed tighter fibrous network in the portions of intraluminal thrombotic material facing the vessel wall, which contained collagen and fibrin fibers, and abundant cells. Cells, evaluated by immunostaining, were present in the whole removed material. Tissue factor expression was also observed with the highest values in the portions of intravascular material facing the vessel wall. In the main pulmonary arteries, SEM images revealed thick fibers of fibrous proteins loosly meshed and few erythrocytes and platelets between them (both dysmorphic "wedged" and fresh cells were present). In the fibrotic layers, containing mainly collagen and fibrin, removed from the lobar/segmental pulmonary arteries we found a stepwise increase in fiber density with decreasing vessel calibre, followed by denser fibrous networks composed of thinner fibers. Elastic fibers in the lobar and segmental arteries were aligned along the blood flow vector. These findings demonstrate differences in the structure of endarterectomized PEA material dependent on the vessel calibre and might contribute to understanding of CTEPH pathophysiology. PMID:27256342

  9. Method for the catalytic conversion of organic materials into a product gas

    DOEpatents

    Elliott, D.C.; Sealock, L.J. Jr.; Baker, E.G.

    1997-04-01

    A method for converting organic material into a product gas includes: (a) providing a liquid reactant mixture containing liquid water and liquid organic material within a pressure reactor; (b) providing an effective amount of a reduced metal catalyst selected from the group consisting of ruthenium, rhodium, osmium and iridium or mixtures thereof within the pressure reactor; and (c) maintaining the liquid reactant mixture and effective amount of reduced metal catalyst in the pressure reactor at temperature and pressure conditions of from about 300 C to about 450 C; and at least 130 atmospheres for a period of time, the temperature and pressure conditions being effective to maintain the reactant mixture substantially as liquid, the effective amount of reduced metal catalyst and the period of time being sufficient to catalyze a reaction of the liquid organic material to produce a product gas composed primarily of methane, carbon dioxide and hydrogen. 5 figs.

  10. Method for the catalytic conversion of organic materials into a product gas

    DOEpatents

    Elliott, Douglas C.; Sealock, Jr., L. John; Baker, Eddie G.

    1997-01-01

    A method for converting organic material into a product gas includes: a) providing a liquid reactant mixture containing liquid water and liquid organic material within a pressure reactor; b) providing an effective amount of a reduced metal catalyst selected from the group consisting of ruthenium, rhodium, osmium and iridium or mixtures thereof within the pressure reactor; and c) maintaining the liquid reactant mixture and effective amount of reduced metal catalyst in the pressure reactor at temperature and pressure conditions of from about 300.degree. C. to about 450.degree. C.; and at least 130 atmospheres for a period of time, the temperature and pressure conditions being effective to maintain the reactant mixture substantially as liquid, the effective amount of reduced metal catalyst and the period of time being sufficient to catalyze a reaction of the liquid organic material to produce a product gas composed primarily of methane, carbon dioxide and hydrogen.

  11. Designing small molecule polyaromatic p- and n-type semiconductor materials for organic electronics

    NASA Astrophysics Data System (ADS)

    Collis, Gavin E.

    2015-12-01

    By combining computational aided design with synthetic chemistry, we are able to identify core 2D polyaromatic small molecule templates with the necessary optoelectronic properties for p- and n-type materials. By judicious selection of the functional groups, we can tune the physical properties of the material making them amenable to solution and vacuum deposition. In addition to solubility, we observe that the functional group can influence the thin film molecular packing. By developing structure-property relationships (SPRs) for these families of compounds we observe that some compounds are better suited for use in organic solar cells, while others, varying only slightly in structure, are favoured in organic field effect transistor devices. We also find that the processing conditions can have a dramatic impact on molecular packing (i.e. 1D vs 2D polymorphism) and charge mobility; this has implications for material and device long term stability. We have developed small molecule p- and n-type materials for organic solar cells with efficiencies exceeding 2%. Subtle variations in the functional groups of these materials produces p- and ntype materials with mobilities higher than 0.3 cm2/Vs. We are also interested in using our SPR approach to develop materials for sensor and bioelectronic applications.

  12. CONTRIBUTION OF SEMI-VOLATILE ORGANIC MATERIAL TO AMBIENT PM2.5

    SciTech Connect

    Delbert J. Eatough; William K. Modey; Rebecca Sizemore; Michael Simpson

    2004-04-01

    Both annual 24-h average and seasonal diurnal samples collected at NETL during the research program have been analyzed. The fine particulate components determined include PM{sub 2.5} mass, ammonium sulfate, ammonium nitrate, elemental and organic carbonaceous material and trace elements. The analysis of the nitrate and organic material includes both the identification of nonvolatile material retained by the particle collection filter and semi-volatile material lost from the particles during sample collection. The results obtained in these analyses indicate that both the semivolatile and nonvolatile organic material in the fine particles sampled at the NETL site originate from mobile emissions in the local area. However, the majority of the nonvolatile material is associated with primary emissions and the majority of the semi-volatile material is secondary, being formed from photochemical processes in the atmosphere. In contrast, the fine particulate sulfate does not originate from the local area but is transported into the study region, mostly from sources in the Ohio River Valley. These observations have been supported by both detailed meteorological and apportionment analysis of the data.

  13. Preparative free-flow electrophoresis as a method of fractionation of natural organic materials

    USGS Publications Warehouse

    Leenheer, J.A.; Malcolm, R.L.

    1973-01-01

    Preparative free-flow electrophoresis was found to be an efficient method of conducting large-scale fractionations of the natural organic polyelectrolytes occurring in many surface waters and soils. The method of free-flow electrophoresis obviates, the problem of adsorption upon a supporting medium and permits the use of high potential gradients and currents because of an efficient cooling system. Separations were monitored by determining organic carbon concentration with a dissolved carbon analyzer, and color was measured by absorbance at 400 nanometers. Organic materials from waters and soils were purified by filtration, hydrogen exchange, and dialysis and were concentrated by freeze drying or freeze concentration. In electrophoretic fractionations of natural organic materials typically found in surface waters and soils, color was found to increase with the charge of the fraction.

  14. Exploration of a calcium-organic framework as an anode material for sodium-ion batteries.

    PubMed

    Zhang, Yan; Niu, Yubin; Wang, Min-Qiang; Yang, Jingang; Lu, Shiyu; Han, Jin; Bao, Shu-Juan; Xu, Maowen

    2016-08-01

    In this communication, we designed and synthesized a novel calcium-organic framework and presented it as an anode material for sodium-ion batteries. The results show that it delivers a reversible capacity of higher than 140 mA h g(-1) even after 300 cycles. The remarkable performance is attributed to the high structural stability and extremely low solubility of the calcium-organic framework in electrolytes. PMID:27440582

  15. Effect of organic materials and rice cultivars on methane emission from rice field.

    PubMed

    Khosa, Maninder Kaur; Sidhu, B S; Benbi, D K

    2010-05-01

    A field experiment was conducted for two years on a sandy loam (Typic Ustochrept) soil of Punjab to study the effect of organic materials and rice cultivars on methane emission from rice fields. The methane flux varied between 0.04 and 0.93 mg m(-2) hr(-1) in bare soil and transplanting of rice crop doubled the methane flux (0.07 to 2.06 mg m(-2) hr(-1)). Among rice cultivars, significantly (p < 0.05) higher amount of methane was emitted from Pusa 44 compared to PR 118 and PR 111. Application of organic materials enhanced methane emission from rice fields and resulted in increased soil organic carbon content. The greatest seasonal methane flux was observed in wheat straw amended plots (229.6 kg ha(-1)) followed by farmyard manure (111.6 kg ha(-1)), green manure (85.4 kg ha(-1)) and the least from rice straw compost amended plots (36.9 kg ha(-1)) as compared to control (21.5 kg ha(-1)). The differential effect of organic materials in enhancing methane flux was related to total carbon or C:N ratio of the material. The results showed that incorporation of humified organic matter such as rice straw compost could minimize methane emission from rice fields with co-benefits of increased soil fertility and crop productivity. PMID:21046997

  16. Interfacial Structures and Properties of Organic Materials for Biosensors: An Overview

    PubMed Central

    Zhou, Yan; Chiu, Cheng-Wei; Liang, Hong

    2012-01-01

    The capabilities of biosensors for bio-environmental monitoring have profound influences on medical, pharmaceutical, and environmental applications. This paper provides an overview on the background and applications of the state-of-the-art biosensors. Different types of biosensors are summarized and sensing mechanisms are discussed. A review of organic materials used in biosensors is given. Specifically, this review focuses on self-assembled monolayers (SAM) due to their high sensitivity and high versatility. The kinetics, chemistry, and the immobilization strategies of biomolecules are discussed. Other representative organic materials, such as graphene, carbon nanotubes (CNTs), and conductive polymers are also introduced in this review. PMID:23202199

  17. Hybrid organic inorganic materials: Layered hydroxy double salts intercalated with substituted thiophene monomers

    NASA Astrophysics Data System (ADS)

    Tronto, Jairo; Leroux, Fabrice; Dubois, Marc; Taviot-Gueho, Christine; Valim, João Barros

    2006-05-01

    The present paper describes the synthesis and characterization of Layered Hydroxy Double Salts (HDSs) containing substituted thiophene anions (2-thiophenecarboxylate, 3-thiophenecarboxylate, and 3-thiopheneacetate). The HDSs host was synthesized via hydrothermal method and the organic anions were incorporated between the sheets by anion-exchange reaction. The materials were characterized by powder X-ray diffraction (PXRD), thermal gravimetric (TG) analysis and electron spin resonance (ESR) spectroscopy. For the 2D-hybrid materials, the basal spacing is found to be consistent with the formation of bilayers of the intercalated organic monomers. For the hybrid material formed after intercalation of 3-thiopheneacetate anion, the ESR signals suggest that the monomers connect each other directly forming small oligomers, whereas this process is not occurring for the two other monomers presenting short alkyl chain. The TG analyses show different stages of thermal decomposition between HDSs host and 2D-hybrid materials, underlining the enhanced thermal stability of the hybrid assembly.

  18. Metal-organic frameworks for electronics: emerging second order nonlinear optical and dielectric materials

    NASA Astrophysics Data System (ADS)

    Mendiratta, Shruti; Lee, Cheng-Hua; Usman, Muhammad; Lu, Kuang-Lieh

    2015-10-01

    Metal-organic frameworks (MOFs) have been intensively studied over the past decade because they represent a new category of hybrid inorganic-organic materials with extensive surface areas, ultrahigh porosity, along with the extraordinary tailorability of structure, shape and dimensions. In this highlight, we summarize the current state of MOF research and report on structure-property relationships for nonlinear optical (NLO) and dielectric applications. We focus on the design principles and structural elements needed to develop potential NLO and low dielectric (low-κ) MOFs with an emphasis on enhancing material performance. In addition, we highlight experimental evidence for the design of devices for low-dielectric applications. These results motivate us to develop better low-dielectric and NLO materials and to perform in-depth studies related to deposition techniques, patterning and the mechanical performance of these materials in the future.

  19. Novel triplet host materials with high energy gap and thermal stability for organic electrophosphorescent devices

    NASA Astrophysics Data System (ADS)

    Qiao, Juan; Wang, Li D.; Qiu, Yong

    2006-04-01

    Organic electrophosphorescent materials and devices are the prime focus of organic light-emitting diodes research due to their high external quantum efficiency and power efficiency. The host materials with both high triplet energy level and high thermal stability are especially formidable for blue phosphorescent emitters. Herewith we report a novel triplet host material based on fluorene, 9,9-bis(4'-carbazol-phenyl)fluorene (CPF), in which two phenyl-carbazole moieties are connected to C9 carbon of the fluorene. This compound possesses not only desirably high triplet (2.9 eV) energies, but also extremely high glass transition temperature (Tg = 165 °C) and thermal stability. By using CPF as the host material, blue-emitting phosphorescent devices exhibited much higher efficiency and longer lifetime than those with CBP host.

  20. Diffraction Studies from Minerals to Organics - Lessons Learned from Materials Analyses

    SciTech Connect

    Whitfield, Pamela S

    2014-01-01

    In many regards the study of materials and minerals by powder diffraction techniques are complimentary, with techniques honed in one field equally applicable to the other. As a long-time materials researcher many of the examples are of techniques developed for materials analysis applied to minerals. However in a couple of cases the study of new minerals was the initiation into techniques later used in materials-based studies. Hopefully they will show that the study of new minerals structures can provide opportunities to add new methodologies and approaches to future problems. In keeping with the AXAA many of the examples have an Australian connection, the materials ranging from organics to battery materials.

  1. Organic Light-Emitting Diodes (OLEDs) and Optically-Detected Magnetic Resonance (ODMR) studies on organic materials

    SciTech Connect

    Cai, Min

    2011-01-01

    Organic semiconductors have evolved rapidly over the last decades and currently are considered as the next-generation technology for many applications, such as organic light-emitting diodes (OLEDs) in flat-panel displays (FPDs) and solid state lighting (SSL), and organic solar cells (OSCs) in clean renewable energy. This dissertation focuses mainly on OLEDs. Although the commercialization of the OLED technology in FPDs is growing and appears to be just around the corner for SSL, there are still several key issues that need to be addressed: (1) the cost of OLEDs is very high, largely due to the costly current manufacturing process; (2) the efficiency of OLEDs needs to be improved. This is vital to the success of OLEDs in the FPD and SSL industries; (3) the lifetime of OLEDs, especially blue OLEDs, is the biggest technical challenge. All these issues raise the demand for new organic materials, new device structures, and continued lower-cost fabrication methods. In an attempt to address these issues, we used solution-processing methods to fabricate highly efficient small molecule OLEDs (SMOLEDs); this approach is costeffective in comparison to the more common thermal vacuum evaporation. We also successfully made efficient indium tin oxide (ITO)-free SMOLEDs to further improve the efficiency of the OLEDs. We employed the spin-dependent optically-detected magnetic resonance (ODMR) technique to study the luminescence quenching processes in OLEDs and organic materials in order to understand the intrinsic degradation mechanisms. We also fabricated polymer LEDs (PLEDs) based on a new electron-accepting blue-emitting polymer and studied the effect of molecular weight on the efficiency of PLEDs. All these studies helped us to better understand the underlying relationship between the organic semiconductor materials and the OLEDs’ performance, and will subsequently assist in further enhancing the efficiency of OLEDs. With strongly improved device performance (in addition to

  2. Organic Light-Emitting Diodes (OLEDs) and Optically-Detected Magnetic Resonance (ODMR) studies on organic materials

    NASA Astrophysics Data System (ADS)

    Cai, Min

    Organic semiconductors have evolved rapidly over the last decades and currently are considered as the next-generation technology for many applications, such as organic light-emitting diodes (OLEDs) in flat-panel displays (FPDs) and solid state lighting (SSL), and organic solar cells (OSCs) in clean renewable energy. This dissertation focuses mainly on OLEDs. Although the commercialization of the OLED technology in FPDs is growing and appears to be just around the corner for SSL, there are still several key issues that need to be addressed: (1) the cost of OLEDs is very high, largely due to the costly current manufacturing process; (2) the efficiency of OLEDs needs to be improved. This is vital to the success of OLEDs in the FPD and SSL industries; (3) the lifetime of OLEDs, especially blue OLEDs, is the biggest technical challenge. All these issues raise the demand for new organic materials, new device structures, and continued lower-cost fabrication methods. In an attempt to address these issues, we used solution-processing methods to fabricate highly efficient small molecule OLEDs (SMOLEDs); this approach is cost-effective in comparison to the more common thermal vacuum evaporation. We also successfully made efficient indium tin oxide (ITO)-free SMOLEDs to further improve the efficiency of the OLEDs. We employed the spin-dependent optically-detected magnetic resonance (ODMR) technique to study the luminescence quenching processes in OLEDs and organic materials in order to understand the intrinsic degradation mechanisms. We also fabricated polymer LEDs (PLEDs) based on a new electron-accepting blue-emitting polymer and studied the effect of molecular weight on the efficiency of PLEDs. All these studies helped us to better understand the underlying relationship between the organic semiconductor materials and the OLEDs' performance, and will subsequently assist in further enhancing the efficiency of OLEDs. With strongly improved device performance (in addition to

  3. [THE THROMBUS FORMATION IN THE PROSTHESIS AS A REACTION OF ORGANISM ON ITS MATERIAL].

    PubMed

    Alekseyeva, T A; Gupalo, Yu M; Kolomoets, A M; Lazarenko, O N; Lazarenko, G O; Litvin, P M; Lohs, I V; Smorzhevskiy, V J; Stepkin, V I

    2016-04-01

    Abstract Vascular prostheses, excised because of their functional properties loss, were studied. Using different methods there was established, that this complication is caused by the thrombus formation as a reaction of organism on the prosthesis material. The testing procedure on compatibility was proposed, using atomic-power microscope. Components of a patient immunity may identify the prosthesis material and start the rejection mechanisms in case of negative reaction. PMID:27434951

  4. Novel Light-Emitting Organic Materials with Variable Electron and Hole Conductivities

    SciTech Connect

    Chen, A.C.-A.; Wallace, J.U.; Zeng, L.; Wei, S.K.-H.; Chen, S.H.

    2005-11-17

    Novel organic materials are constructed by attaching monodisperse oligofluorenes to a hole- or an electron-conducting core through a flexible spacer. These materials exhibit desirable properties for use in polarized and unpolarized light-emitting diodes, such as the ability to form morphologically stable glassy liquid crystalline and amorphous films with elevated glass transition temperatures, capability for full-color emission, tunability of charge injection and transport, and ultimately achieving superior OLED device efficiency and lifetime.

  5. Low consumption power variable optical attenuator with sol-gel derived organic/inorganic hybrid materials

    NASA Astrophysics Data System (ADS)

    Li, Dongxiao; Zhang, Yanwu; Liu, Liying; Xu, Lei

    2006-06-01

    An integrated optical waveguide variable optical attenuator (VOA) made of organic/inorganic hybrid materials was fabricated. At 1550 nm, the VOA showed a very low activation power of about 13 mW, due to the large thermo-optic coefficients of the hybrid materials. The optical power attenuations achieved were more than 25 dB for both TE and TM polarization. The response time of the device was less than 4.7 ms.

  6. Explorating coupled production of dissolved organic material and methyl mercury in a tidal wetland using the intrinsic chemical composition of the organic material

    NASA Astrophysics Data System (ADS)

    Bergamaschi, B. A.; Fleck, J. A.; Downing, B.; Stephenson, M.; Hernes, P. J.; Boss, E.

    2007-12-01

    Elevated methyl mercury (MeHg) levels found in biota of the San Francisco Estuary have been attributed to methylation processes in the peat-rich tidal wetlands of the Estuary, where the concentration of dissolved organic matter (DOM) is tightly coupled to that of MeHg (r2=0.95). We sought to understand the geochemical processes that contribute to MeHg production by examining the composition of the co-occurring DOM. We measured spectral absorbance and fluorescence properties of DOM, as well as intrinsic chemical properties such as isotopic composition, lignin content, carbohydrate content, and bulk chemical functionality (by CPMAS-NMR). Carbon quality parameters independent of concentration such as specific UV absorbance, lignin abundance, aromatic content, biodegradability, and others were closely coupled to MeHg concentrations. This coupling, combined with the hydrologic forcing within the wetland, suggest that the zones of MeHg production are biogeochemically related to the zones of DOM release, thus providing a means to examine the underlying processes. The observed relationships were robust through the winter, spring, and fall seasons, despite a three- fold variation in MeHg and DOM concentration. The pattern of variation suggests sources of DOM and MeHg within peat pore waters rather than within the litter layer or water column. The various relationships with individual parameters will be discussed.

  7. Scalable Sub-micron Patterning of Organic Materials Toward High Density Soft Electronics

    PubMed Central

    Kim, Jaekyun; Kim, Myung-Gil; Kim, Jaehyun; Jo, Sangho; Kang, Jingu; Jo, Jeong-Wan; Lee, Woobin; Hwang, Chahwan; Moon, Juhyuk; Yang, Lin; Kim, Yun-Hi; Noh, Yong-Young; Yun Jaung, Jae; Kim, Yong-Hoon; Kyu Park, Sung

    2015-01-01

    The success of silicon based high density integrated circuits ignited explosive expansion of microelectronics. Although the inorganic semiconductors have shown superior carrier mobilities for conventional high speed switching devices, the emergence of unconventional applications, such as flexible electronics, highly sensitive photosensors, large area sensor array, and tailored optoelectronics, brought intensive research on next generation electronic materials. The rationally designed multifunctional soft electronic materials, organic and carbon-based semiconductors, are demonstrated with low-cost solution process, exceptional mechanical stability, and on-demand optoelectronic properties. Unfortunately, the industrial implementation of the soft electronic materials has been hindered due to lack of scalable fine-patterning methods. In this report, we demonstrated facile general route for high throughput sub-micron patterning of soft materials, using spatially selective deep-ultraviolet irradiation. For organic and carbon-based materials, the highly energetic photons (e.g. deep-ultraviolet rays) enable direct photo-conversion from conducting/semiconducting to insulating state through molecular dissociation and disordering with spatial resolution down to a sub-μm-scale. The successful demonstration of organic semiconductor circuitry promise our result proliferate industrial adoption of soft materials for next generation electronics. PMID:26411932

  8. Scalable sub-micron patterning of organic materials toward high density soft electronics

    SciTech Connect

    Kim, Jaekyun; Kim, Myung -Gil; Kim, Jaehyun; Jo, Sangho; Kang, Jingu; Jo, Jeong -Wan; Lee, Woobin; Hwang, Chahwan; Moon, Juhyuk; Yang, Lin; Kim, Yun -Hi; Noh, Yong -Young; Yun Jaung, Jae; Kim, Yong -Hoon; Kyu Park, Sung

    2015-09-28

    The success of silicon based high density integrated circuits ignited explosive expansion of microelectronics. Although the inorganic semiconductors have shown superior carrier mobilities for conventional high speed switching devices, the emergence of unconventional applications, such as flexible electronics, highly sensitive photosensors, large area sensor array, and tailored optoelectronics, brought intensive research on next generation electronic materials. The rationally designed multifunctional soft electronic materials, organic and carbon-based semiconductors, are demonstrated with low-cost solution process, exceptional mechanical stability, and on-demand optoelectronic properties. Unfortunately, the industrial implementation of the soft electronic materials has been hindered due to lack of scalable fine-patterning methods. In this report, we demonstrated facile general route for high throughput sub-micron patterning of soft materials, using spatially selective deep-ultraviolet irradiation. For organic and carbon-based materials, the highly energetic photons (e.g. deep-ultraviolet rays) enable direct photo-conversion from conducting/semiconducting to insulating state through molecular dissociation and disordering with spatial resolution down to a sub-μm-scale. As a result, the successful demonstration of organic semiconductor circuitry promise our result proliferate industrial adoption of soft materials for next generation electronics.

  9. Scalable sub-micron patterning of organic materials toward high density soft electronics

    DOE PAGESBeta

    Kim, Jaekyun; Kim, Myung -Gil; Kim, Jaehyun; Jo, Sangho; Kang, Jingu; Jo, Jeong -Wan; Lee, Woobin; Hwang, Chahwan; Moon, Juhyuk; Yang, Lin; et al

    2015-09-28

    The success of silicon based high density integrated circuits ignited explosive expansion of microelectronics. Although the inorganic semiconductors have shown superior carrier mobilities for conventional high speed switching devices, the emergence of unconventional applications, such as flexible electronics, highly sensitive photosensors, large area sensor array, and tailored optoelectronics, brought intensive research on next generation electronic materials. The rationally designed multifunctional soft electronic materials, organic and carbon-based semiconductors, are demonstrated with low-cost solution process, exceptional mechanical stability, and on-demand optoelectronic properties. Unfortunately, the industrial implementation of the soft electronic materials has been hindered due to lack of scalable fine-patterning methods. Inmore » this report, we demonstrated facile general route for high throughput sub-micron patterning of soft materials, using spatially selective deep-ultraviolet irradiation. For organic and carbon-based materials, the highly energetic photons (e.g. deep-ultraviolet rays) enable direct photo-conversion from conducting/semiconducting to insulating state through molecular dissociation and disordering with spatial resolution down to a sub-μm-scale. As a result, the successful demonstration of organic semiconductor circuitry promise our result proliferate industrial adoption of soft materials for next generation electronics.« less

  10. Scalable Sub-micron Patterning of Organic Materials Toward High Density Soft Electronics

    NASA Astrophysics Data System (ADS)

    Kim, Jaekyun; Kim, Myung-Gil; Kim, Jaehyun; Jo, Sangho; Kang, Jingu; Jo, Jeong-Wan; Lee, Woobin; Hwang, Chahwan; Moon, Juhyuk; Yang, Lin; Kim, Yun-Hi; Noh, Yong-Young; Yun Jaung, Jae; Kim, Yong-Hoon; Kyu Park, Sung

    2015-09-01

    The success of silicon based high density integrated circuits ignited explosive expansion of microelectronics. Although the inorganic semiconductors have shown superior carrier mobilities for conventional high speed switching devices, the emergence of unconventional applications, such as flexible electronics, highly sensitive photosensors, large area sensor array, and tailored optoelectronics, brought intensive research on next generation electronic materials. The rationally designed multifunctional soft electronic materials, organic and carbon-based semiconductors, are demonstrated with low-cost solution process, exceptional mechanical stability, and on-demand optoelectronic properties. Unfortunately, the industrial implementation of the soft electronic materials has been hindered due to lack of scalable fine-patterning methods. In this report, we demonstrated facile general route for high throughput sub-micron patterning of soft materials, using spatially selective deep-ultraviolet irradiation. For organic and carbon-based materials, the highly energetic photons (e.g. deep-ultraviolet rays) enable direct photo-conversion from conducting/semiconducting to insulating state through molecular dissociation and disordering with spatial resolution down to a sub-μm-scale. The successful demonstration of organic semiconductor circuitry promise our result proliferate industrial adoption of soft materials for next generation electronics.

  11. Scalable Sub-micron Patterning of Organic Materials Toward High Density Soft Electronics.

    PubMed

    Kim, Jaekyun; Kim, Myung-Gil; Kim, Jaehyun; Jo, Sangho; Kang, Jingu; Jo, Jeong-Wan; Lee, Woobin; Hwang, Chahwan; Moon, Juhyuk; Yang, Lin; Kim, Yun-Hi; Noh, Yong-Young; Jaung, Jae Yun; Kim, Yong-Hoon; Park, Sung Kyu

    2015-01-01

    The success of silicon based high density integrated circuits ignited explosive expansion of microelectronics. Although the inorganic semiconductors have shown superior carrier mobilities for conventional high speed switching devices, the emergence of unconventional applications, such as flexible electronics, highly sensitive photosensors, large area sensor array, and tailored optoelectronics, brought intensive research on next generation electronic materials. The rationally designed multifunctional soft electronic materials, organic and carbon-based semiconductors, are demonstrated with low-cost solution process, exceptional mechanical stability, and on-demand optoelectronic properties. Unfortunately, the industrial implementation of the soft electronic materials has been hindered due to lack of scalable fine-patterning methods. In this report, we demonstrated facile general route for high throughput sub-micron patterning of soft materials, using spatially selective deep-ultraviolet irradiation. For organic and carbon-based materials, the highly energetic photons (e.g. deep-ultraviolet rays) enable direct photo-conversion from conducting/semiconducting to insulating state through molecular dissociation and disordering with spatial resolution down to a sub-μm-scale. The successful demonstration of organic semiconductor circuitry promise our result proliferate industrial adoption of soft materials for next generation electronics. PMID:26411932

  12. Superconductivity and Magnetism in Organic Materials Studied with μSR

    NASA Astrophysics Data System (ADS)

    Pratt, Francis

    2016-09-01

    A review is given of the current status and recent progress in the use of μSR for the study of superconductivity and magnetism in organic materials. For organic superconductors, important factors are discussed that influence the observed μSR line widths and their field and temperature dependences in the superconducting state. The accumulated μSR results give direct information about the scaling relationship between superfluid stiffness and transition temperature that provides a strong constraint for theories of organic superconductors. For organic magnetism, μSR offers a sensitive probe for detecting various weak magnetic phenomena ranging from spin-density-wave transitions through spin dynamics and 3D ordering of Heisenberg chain systems to field induced magnetism of quantum spin liquids. Finally, experiments are described that focus on two current issues in organic spintronics: direct measurement of the spin coherence length and the identification of the relative importance of different mechanisms of spin decoherence.

  13. Assessment of survivability of liquid water and organic materials through modeling of large-scale impacts

    NASA Astrophysics Data System (ADS)

    Blank, Jennifer

    Comets, estimated to contain up to 25 wt.% organic material as both ices and more complex, refractory compounds, have been proposed as a vehicle for the delivery of organic compounds to the early Earth and other rocky planets. Successful delivery requires that some of the organic materials survive the extreme temperatures associated with impact, but the response of organic compounds to impact (shock) processing under these conditions is unknown. Several researchers have explored organic-delivery scenarios computationally and experimentally. Here, I will summarize work that addresses the issue of impact delivery and focus on current efforts to track the phase-state of water during a modeled comet-earth collision over a range of impact angles. On the basis of model results generated using a three-dimensional shock physics code (GEODYN), I will infer survivability of organic compounds and liquid water in a range of impact scenarios for comet-Earth and asteroid-Earth collisions. These results will be described in the context of the flux of astromaterials, and organic matter in particular, to young planets.

  14. Potential of organic filter materials for treating greywater to achieve irrigation quality: a review.

    PubMed

    Dalahmeh, Sahar S; Hylander, Lars D; Vinnerås, Björn; Pell, Mikael; Oborn, Ingrid; Jönsson, Håkan

    2011-01-01

    The objectives of this literature review were to: (i) evaluate the impact of greywater generated in rural communities, with the emphasis on Jordanian conditions, on soil, plant and public health and assess the need for treatment of this greywater before it is used for irrigation, and (ii) assess the potential of different types of organic by-products as carrier material in different filter units for removal of pollutants from greywater. Greywater with high BOD5, COD, high concentrations of SS, fat, oil and grease and high levels of surfactants is commonly found in rural areas in Jordan. Oxygen depletion, odour emission, hydrophobic soil phenomena, plant toxicity, blockage of piping systems and microbiological health risks are common problems associated with greywater without previous treatment. Organic by-products such as wood chips, bark, peat, wheat straw and corncob may be used as carrier material in so-called mulch filters for treating wastewater and greywater from different sources. A down-flow-mode vertical filter is a common setup used in mulch filters. Wastewaters with a wide range of SS, cBOD5 and COD fed into different mulch filters have been studied. The different mulch materials achieved SS removal ranging between 51 and 91%, a BOD5 reduction range of 55-99.9%, and COD removal of 51-98%. Most types of mulches achieved a higher organic matter removal than that achieved by an ordinary septic tank. Bark, peat and wood chips filters removed organic matter better than sand and trickling filters, under similar conditions. Release of filter material and increase in COD in the effluent was reported using some mulch materials. In conclusion, some mulch materials such as bark, peat and woodchips seem to have a great potential for treatment of greywater in robust, low-tech systems. They can be expected to be resilient in dealing with variable low and high organic loads and shock loads. PMID:21902020

  15. [Vermicomposting of different organic materials and three-dimensional excitation emission matrix fluorescence spectroscopic characterization of their dissolved organic matter].

    PubMed

    Yang, Wei; Wang, Dong-sheng; Liu, Man-qiang; Hu, Feng; Li, Hui-xin; Huang, Zhong-yang; Chang, Yi-jun; Jiao, Jia-guo

    2015-10-01

    In this experiment, different proportions of the cattle manure, tea-leaf, herb and mushroom residues, were used as food for earthworm (Eisenia fetida) to study the growth of the earth-worm. Then the characteristics and transformation of nutrient content and three-dimensional excitation emission matrix fluorescence (3DEEM) of dissolved organic matter (DOM) during vermistabilization were investigated by means of chemical and spectroscopic methods. The result showed that the mixture of different ratios of cattle manure with herb residue, and cattle manure with tea-leaf were conducive to the growth of earthworm, while the materials compounded with mushroom residue inhibited the growth of earthworm. With the increasing time of verimcomposting, the pH in vermicompost tended to be circumneutral and weakly acidic, and there were increases in electrical conductivity, and the contents of total nitrogen, total phosphorus, available nitrogen, and available phosphorus, while the total potassium and available potassium increased first and then decreased, and the organic matter content decreased. 3DEEM and fluorescence regional integration results indicated that, the fluorescence of protein-like fluorescence peaks declined significantly, while the intensity of humic-like fluorescence peak increased significantly in DOM. Vermicomposting process might change the compositions of DOM with elevated concentrations of humic acid and fulvic acid in the organics. In all, this study suggested the suitability of 3DEEM for monitoring the organics transformation and assessing the maturity in the vermicomposting. PMID:26995929

  16. Self-aligned optical couplings by self-organized waveguides toward luminescent targets in organic/inorganic hybrid materials.

    PubMed

    Yoshimura, Tetsuzo; Iida, Makoto; Nawata, Hideyuki

    2014-06-15

    Self-organization of optical waveguides is observed between two opposed optical fibers placed in a photosensitive organic/inorganic hybrid material, Sunconnect. A luminescent target containing coumarin 481 was deposited onto the edge of one of the two fibers at the core. When a 448-nm write beam was introduced from the other fiber, the write beam and the luminescence from the photoexcited target increased the refractive index of Sunconnect to induce self-focusing. Traces of waveguides were seen to grow from the cores of both fibers and merged into a single self-aligned optical coupling between the fibers. This optical solder functionality enabled increases in both coupling efficiency and tolerance to lateral misalignment of the fibers. PMID:24978520

  17. Guard Flow-enhanced Organic Vapor Jet Printing of Molecular Materials in Air

    NASA Astrophysics Data System (ADS)

    Biswas, Shaurjo

    Rapid advances in the research and development of organic electronics have re-sulted in many exciting discoveries and applications, including OLEDs, OPVs and OTFTs. Devices based on small molecular organic materials often call for sharp interfaces and highly pure materials for improved device performance. Solvent-free deposition and additive patterning of the active layers without the use of vacuum is preferred, calling for specialized processing approaches. Guard flow-enhanced organic vapor jet printing (GF-OVJP), enables addi-tive, rapid, mask-free, solvent-free printing of molecular organic semiconductors in ambient atmosphere by evaporating organic source material into an inert carrier gas jet and collimating and impinging it onto a substrate where the organic molecules condense. A surrounding annular "guard flow" hydrodynamically focuses the primary jet carrying the hot organic vapor and shields it from contact with the ambient oxygen and moisture, enabling device-quality deposits. Deposition in air entails non-trivial effects at the boundary between ambient surroundings and the gas jet carrying the semiconductor vapor that influence the morphology and properties of the resulting electronic devices. This thesis demonstrates the deposition of active layers of OLEDs, OPVs and OTFTs by GF-OVJP in air. Process-structure-property relationships are elucidated, using a combination of film deposition and structural characterization (e.g. AFM, XRD, SEM, spectroscopies), device fabrication and testing, as well as compressible fluid flow, heat and mass transport modeling, thus laying the groundwork for rigorous, quantitative design of film deposition apparatus and small molecular organic semiconductor processing.

  18. Introduction of bridging and pendant organic groups into mesoporous alumina materials.

    PubMed

    Grant, Stacy M; Woods, Stephan M; Gericke, Arne; Jaroniec, Mietek

    2011-11-01

    Incorporation of organic functionalities into soft-templated mesoporous alumina was performed via organosilane-assisted evaporation induced self-assembly using aluminum alkoxide precursors and block copolymer templates. This strategy permits one to obtain mesoporous alumina-based materials with tailorable adsorption, surface and structural properties. Isocyanurate, ethane, mercaptopropyl, and ureidopropyl-functionalized mesoporous alumina materials were synthesized with relatively high surface area and large pore volume with uniform and wormhole-like mesopores. The presence of organosilyl groups within these hybrid materials was confirmed by IR or Raman spectroscopy and their concentration was determined by elemental analysis. PMID:21988174

  19. Relative Humidity and Temperature Effects on the Viscosity of Secondary Organic Material from α-pinene Ozonolysis

    NASA Astrophysics Data System (ADS)

    Wolff, L. R.; Grayson, J. W.; Bateman, A. P.; Kuwata, M.; Sellier, M.; Murray, B. J.; Shilling, J. E.; Martin, S. T.; Bertram, A. K.

    2013-12-01

    Secondary organic aerosol particles are abundant in the troposphere, comprising the majority of the total particle mass in some areas. Secondary organic particles may play an important role in climate, air quality, and health. Particle viscosity may influence atmospheric particle sizes and concentrations in the troposphere, as well as reaction rates with various atmospheric oxidants. A quantitative measure of particle viscosity is needed in order to predict the effects of particle viscosity on various atmospheric processes. To date, the viscosities of atmospheric particles including SOA particles remains poorly understood. Furthermore, the relative humidity and temperature dependence of the particle viscosities remain uncertain. A major obstacle to measuring viscosities of atmospheric or environmental chamber samples is the small sample volumes typically collected from these media (on the order of milligrams after long collection times). The minimum sample volumes required for existing microviscometry techniques are on the order of 10's of μL's and are limited to measuring viscosities of low-viscosity liquids (<0.1 Pa s). Other existing viscometers for measuring higher viscosities require much greater sample volumes. Presented here are the results of two novel approaches to measuring the viscosity of organic aerosol particles, which together are capable of measuring a wide range of viscosities using significantly less than 1mg of material. These techniques are applied across the ambient tropospheric RH range. A third technique is used to determine the extent to which the particle viscosity may change over a wide range of tropospheric temperatures (-10 to 20 degrees C). These techniques not only provide visual evidence that the water-soluble fraction of atmospheric samples may behave as semi-solids or solids under tropospheric relative humidity and temperature conditions, but also provide quantitative information as to their viscosities.

  20. The Effects of Ground and Space Processing on the Properties of Organic, Polymeric, and Colloidal Materials

    NASA Technical Reports Server (NTRS)

    Frazier, Donald O.; Penn, Benjamin G.; Paley, M. S.; Abdeldayem, Hossain A.; Witherow, W. K.; Smith, D.

    1998-01-01

    In recent years, a great deal of interest has been directed toward the use of organic materials in the development of high-efficiency optoelectronic and phototonic devices. There is a myriad of possibilities among organic materials which allow flexibility in the design of unique structures with a variety of functional groups. The use of nonlinear optical (NLO) organic materials as thin film wave-guides allows full exploitation of their desirable qualifies by permitting long interaction lengths and large susceptibilities allowing modest power input. There are several methods in use to prepare thin films such as Langmuir-Blodgett (LB) and self-assembly techniques, vapor deposition, growth from sheared solution or melt, and melt growth between glass plates. Organic-based materials have many features that make them desirable for use in optical devices, such as high second-and third-order nonlinearity, flexibility of molecular design, and damage resistance to optical radiation. However, their use in devices has been hindered by processing difficulties for crystals and thin films. We discuss the potential role of microgravity processing of a few organic and polymeric materials. It is of interest to note how materials with second-and third-order NLO behavior may be improved in a diffusion-limited environment and ways in which convection may be detrimental to these materials. We focus our discussion on third-order materials for all-optical switching, and second-order materials for frequency conversion and electrooptics. The goal of minimizing optical loss obviously depends on processing methods. For solution-based processes, such as solution crystal growth and solution photopolymerization, it is well known that thermal and solutal density gradients can initiate buoyancy-driven convection. Resultant fluid flows can affect transport of material to and from growth interfaces and become manifest in the morphology and homogeneity of the growing film or crystal. Likewise

  1. Pyrolysis characteristics and pyrolysis products separation for recycling organic materials from waste liquid crystal display panels.

    PubMed

    Wang, Ruixue; Xu, Zhenming

    2016-01-25

    Waste liquid crystal display (LCD) panels mainly contain inorganic materials (glass substrate with indium-tin oxide film), and organic materials (polarizing film and liquid crystal). The organic materials should be removed beforehand since the organic matters would hinder the indium recycling process. In the present study, pyrolysis process is used to remove the organic materials and recycle acetic as well as and triphenyl phosphate (TPP) from waste LCD panels in an environmental friendly way. Several highlights of this study are summarized as follows: (i) Pyrolysis characteristics and pyrolysis kinetics analysis are conducted which is significant to get a better understanding of the pyrolysis process. (ii) Optimum design is developed by applying Box-Behnken Design (BBD) under response surface methodology (RSM) for engineering application which is significant to guide the further industrial recycling process. The oil yield could reach 70.53 wt% and the residue rate could reach 14.05 wt% when the pyrolysis temperature is 570 °C, nitrogen flow rate is 6 L min(-1) and the particle size is 0.5 mm. (iii) Furthermore, acetic acid and TPP are recycled, and then separated by rotary evaporation, which could reduce the consumption of fossil energy for producing acetic acid, and be reused in electronics manufacturing industry. PMID:26444486

  2. INTERLABORATORY METHODS COMPARISON FOR THE TOTAL ORGANIC CARBON ANALYSIS OF AQUIFER MATERIALS

    EPA Science Inventory

    The total organic carbon (TOC) content of aquifer materials has been found to have significant effects on the movement of pollutants in the subsurface environment. Accurate quantification of TOC is therefore of great importance to research in groundwater contamination. owever, la...

  3. Using Organic Light-Emitting Electrochemical Thin-Film Devices to Teach Materials Science

    ERIC Educational Resources Information Center

    Sevian, Hannah; Muller, Sean; Rudmann, Hartmut; Rubner, Michael F.

    2004-01-01

    Materials science can be taught by applying organic light-emitting electrochemical thin-film devices and in this method students were allowed to make a light-emitting device by spin coating a thin film containing ruthenium (II) complex ions onto a glass slide. Through this laboratory method students are provided with the opportunity to learn about…

  4. Nanosized titanium dioxide reduces copper toxicity--the role of organic material and the crystalline phase.

    PubMed

    Rosenfeldt, Ricki R; Seitz, Frank; Senn, Lilli; Schilde, Carsten; Schulz, Ralf; Bundschuh, Mirco

    2015-02-01

    Titanium dioxide nanoparticles (nTiO2) are expected to interact with natural substances and other chemicals in the environment, however little is known about their combined effects. Therefore, this study assessed the toxicity of copper (Cu) in combination with varying crystalline phases (anatase, rutile, and the mixture) of nTiO2 and differing organic materials on Daphnia magna. The nanoparticles reduced the Cu-toxicity depending on the product (0.3- to 2-fold higher 48-h EC50). This decrease in toxicity coincided with a lowered Cu-concentration in the water column, which was driven by the adsorption of Cu to nTiO2-depending on available surface area and structure-and their subsequent sedimentation. In the presence of organic material and nTiO2, the Cu-toxicity was further reduced (up to 7-fold higher 48-h EC50). This observation can be explained by a reduced Cu-bioavailability as a result of complexation and adsorption by the organic material and nTiO2, respectively. Thus, the crystalline phase composition, which is determining the surface area and structure of nTiO2, seems to be of major importance for the toxicity reduction of heavy metals, while the influence of the organic materials was mainly driven by the quantity and quality of humic substances. PMID:25556663

  5. Effects of surfactants on the desorption of organic contaminants from aquifer materials. Doctoral thesis

    SciTech Connect

    Brickell, J.L.

    1989-08-01

    The efficiency of removing organic contaminants from groundwater aquifers by the pump and treat process is adversely affected by the retardation of the contaminant's mobility due to adsorption onto aquifer material. The use of surfactants in conjunction with the pump and treat process has the potential for improving contaminant mobility by solubilizing the adsorbed contaminant.

  6. Compost feedstock characteristics and ratio modelling for organic waste materials co-composting in Malaysia.

    PubMed

    Chai, E W; H'ng, P S; Peng, S H; Wan-Azha, W M; Chin, K L; Chow, M J; Wong, W Z

    2013-01-01

    In Malaysia, large amounts of organic materials, which lead to disposal problems, are generated from agricultural residues especially from palm oil industries. Increasing landfill costs and regulations, which limit many types of waste accepted at landfills, have increased the interest in composting as a component of waste management. The objectives of this study were to characterize compost feedstock properties of common organic waste materials available in Malaysia. Thus, a ratio modelling of matching ingredients for empty fruit bunches (EFBs) co-composting using different organic materials in Malaysia was done. Organic waste materials with a C/N ratio of < 30 can be applied as a nitrogen source in EFB co-composting. The outcome of this study suggested that the percentage of EFB ranged between 50% and 60%, which is considered as the ideal mixing ratio in EFB co-composting. Conclusively, EFB can be utilized in composting if appropriate feedstock in term of physical and chemical characteristics is coordinated in the co-composting process. PMID:24527651

  7. Effects of the Integrated Online Advance Organizer Teaching Materials on Students' Science Achievement and Attitude

    ERIC Educational Resources Information Center

    Korur, Fikret; Toker, Sacip; Eryilmaz, Ali

    2016-01-01

    This two-group quasi-experimental study investigated the effects of the Online Advance Organizer Concept Teaching Material (ONACOM) integrated with inquiry teaching and expository teaching methods. Grade 7 students' posttest performances on the light unit achievement and light unit attitude tests controlled for gender, previous semester science…

  8. AUDIT MATERIALS FOR SEMIVOLATILE ORGANIC MEASUREMENTS DURING HAZARDOUS WASTE TRIAL BURNS

    EPA Science Inventory

    Two new performance audit materials utilizing different sorbents have neen developed to assess the overall accuracy and precision of the sampling, desorption, and analysis of semivolatile organic compounds by EPA, SW 846 Method 0010 (i.e., the Modified Method 5 sampling train). h...

  9. 9 CFR 95.17 - Glands, organs, ox gall, and like materials; requirements for unrestricted entry.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 9 Animals and Animal Products 1 2013-01-01 2013-01-01 false Glands, organs, ox gall, and like materials; requirements for unrestricted entry. 95.17 Section 95.17 Animals and Animal Products ANIMAL AND PLANT HEALTH INSPECTION SERVICE, DEPARTMENT OF AGRICULTURE EXPORTATION AND IMPORTATION OF ANIMALS (INCLUDING POULTRY) AND ANIMAL PRODUCTS...

  10. INTERLABORATORY METHODS COMPARISON FOR THE TOTAL ORGANIC CARBON ANALYSIS OF AQUIFER MATERIALS

    EPA Science Inventory

    The total organic carbon (TOC) content of aquifer materials has been found to have significant effects on the movement of pollutants in the subsurface environment. Accurate quantification of TOC is therefore of great im- portance to research in groundwater contamination. However,...

  11. How Microstructure Defines Function in Organic Conjugated Materials: Insights from Modelling

    NASA Astrophysics Data System (ADS)

    Olivier, Yoann

    Organic conjugated materials have attracted an increasing interest over the years for their use in organic opto- electronic devices such as light-emitting diodes, solar cells, or field- effect transistors as a result of their low cost, light weight and ease of processing from solution. The improvement of the device performances requires a deep understanding of the electronic processes taking place in these devices down to the molecular scale. Especially, the way organic conjugated molecules or polymer chains organize in the solid state appears as a critical parameter to control in order to fine tune the materials electronic and photophysical properties. In our laboratory, we have developed a multi-faceted modeling scheme that encompasses classical molecular dynamics, quantum-chemistry, non-adiabatic quantum dynamics and kinetic Monte Carlo simulations to assess multiple fundamental opto- electronic processes occurring in conjugated materials used in devices. Here, we will more specifically review work dealing with the modeling of charge transport in conjugated polymers as well as singlet fission and exciton transport in small molecules. In all cases, we will highlight how these processes are sensitive to the relative arrangement of the materials at the nanoscale.

  12. 77 FR 12202 - Public Inspection of Material Relating to Tax-Exempt Organizations

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-02-29

    ... Register (72 FR 45394-01) on August 14, 2007. One comment was received from the public in response to the... status filed by the political organization shall be open to public inspection. (c) Letters or documents... Internal Revenue Service 26 CFR Part 301 RIN 1545-BG60 Public Inspection of Material Relating to...

  13. Graphitization of Organic Material in a Progressively Metamorphosed Precambrian Iron Formation.

    PubMed

    French, B M

    1964-11-13

    Organic matter in the sedimentary Biwabik iron formation in northern Minnesota shows a progressive increase in crystallinity where the formation is metamorphosed by the intrusive Duluth gabbro complex. X-ray diffraction of acid-insoluble residues shows that there is a complete range in crystallinity, from amorphous material in the unmetamorphosed sediments to completely crystalline graphite adjacent to the gabbro. PMID:17777057

  14. Water holding capacity and evaporative loss from organic bedding materials used in livestock facilities

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Physical and chemical characteristics of organic bedding materials determine how well they will absorb and retain moisture and may influence the environment in livestock facilities where bedding is used. The objective of this study was to determine water holding capacity (WHC) and rate of evaporativ...

  15. 9 CFR 95.17 - Glands, organs, ox gall, and like materials; requirements for unrestricted entry.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 9 Animals and Animal Products 1 2014-01-01 2014-01-01 false Glands, organs, ox gall, and like materials; requirements for unrestricted entry. 95.17 Section 95.17 Animals and Animal Products ANIMAL AND PLANT HEALTH INSPECTION SERVICE, DEPARTMENT OF AGRICULTURE EXPORTATION AND IMPORTATION OF ANIMALS (INCLUDING POULTRY) AND ANIMAL PRODUCTS...

  16. Advantage of terahertz radiation versus X-ray to detect hidden organic materials in sealed vessels

    NASA Astrophysics Data System (ADS)

    Bessou, Maryelle; Duday, Henri; Caumes, Jean-Pascal; Salort, Simon; Chassagne, Bruno; Dautant, Alain; Ziéglé, Anne; Abraham, Emmanuel

    2012-10-01

    Terahertz imaging and conventional X-ray have been used to investigate a sealed Ancient Egyptian jar preserved at the Museum of Aquitaine (France). Terahertz radiation revealed an unknown content that could not have been visualized by X-ray. By comparison with a model object, we concluded that this content was composed of organic materials explaining their relative radiolucency.

  17. USE OF CATIONIC SURFACTANTS TO MODIFY AQUIFER MATERIALS TO REDUCE THE MOBILITY OF HYDROPHOBIC ORGANIC COMPOUNDS

    EPA Science Inventory

    Cationic surfactants can be used to modify surfaces of soils and subsurface materials to promote sorption of hydrophobic organic compounds (HOC) and retard their migration. or example, cationic surfactants could be injected into an aquifer downgradient from a source of HOC contam...

  18. Metal-organic magnetic materials based on cobalt phthalocyanine and possibilities of their application in medicine

    NASA Astrophysics Data System (ADS)

    Harutyunyan, Avetik R.; Kuznetsov, Anatoly A.; Kuznetsov, Oleg A.; Kaliya, O. L.

    1999-04-01

    Cobalt phthalocyanines (CoPc), doped with sodium, exhibit ferromagnetic ordering at room temperature. Magnetic dilution or variation in dopant concentration leads to the formation of new magnetic materials. A proposed scheme of oncological disease treatment includes magnetic concentration of CoPc particles in the tumor zone and ascorbic acid injection into the organism for stimulation of oxidation reactions, which destroy the tumor.

  19. Sorption of trace organics and engineered nanomaterials onto wetland plant material.

    PubMed

    Sharif, Fariya; Westerhoff, Paul; Herckes, Pierre

    2013-01-01

    Wastewater treatment plant (WWTP) effluents are sources for emerging pollutants, including organic compounds and engineered nanomaterials (ENMs), which then flow into aquatic systems. In this article, natural attenuation of pollutants by constructed wetland plants was investigated using lab-scale microcosm and batch sorption studies. The microcosms were operated at varying hydraulic residence times (HRTs) and contained decaying plant materials. Representative organic compounds and ENMs were simultaneously spiked into the microcosm influent, along with a conservative tracer (bromide), and then monitored in the effluent over time. It was observed that a more hydrophobic compound-natural estrogen achieved better removal than a polar organic compound – para-chlorobenzoic acid (pCBA), which mimics the behaviour of the tracer. Batch sorption experiments showed that estrogen has higher sorption affinity than pCBA, highlighting the importance of sorption to the plant materials as a removal process for the organic contaminants in the microcosms. Wetland plants were also found a potential sorbent for ENMs. Two different ENMs (nano-silver and aqueous fullerenes) were included in this study, both of which experienced comparable removal in the microcosms. Relative to the tracer, the highest removal of ENMs and trace organics was 60% and 70%, respectively. A more than two-fold increase in HRT increased the removal efficiency of the contaminants in the range of 20–60%. The outcome of this study supports that plant materials of wetlands can play an important role in removing emerging pollutants from WWTP effluent. PMID:24592444

  20. Facile Preparation of Bright-Fluorescent Soft Materials from Small Organic Molecules.

    PubMed

    Wang, Hang-Xing; Yang, Ze; Liu, Zhong-Guo; Wan, Jia-Yun; Xiao, Juan; Zhang, Hao-Li

    2016-06-01

    Highly fluorescent and biocompatible soft materials are desirable for many potential applications, but their synthetic processes are somehow complicated. Herein, we have explored the feasibility of synthesis of unconventional fluorescence soft materials from small organic molecules under mild conditions. A new blue-fluorescent soft material with high quantum yield (89.6 %) and eutectic feature prepared by simple heat treatment of citric acid (CA) and cysteine (Cys) aqueous mixtures below 100 °C in air was reported. The as-prepared fluorescent material has the features of facile preparation, low cost, scalable production and easy to process, making it suitable for applications like fluorescent labeling and light-emitting devices. This new finding opens a new venue for the preparation of fluorescent soft materials. PMID:27194639

  1. Distribution and compositional change of organic materials with the evolution or a protoplanetary disk

    NASA Astrophysics Data System (ADS)

    Nagahara, Hiroko

    2015-08-01

    A protoplanetary disk evolves dynamically, which changes the physical and chemical conditions temporally and spatially. Evolution of organic materials derived from the previous molecular cloud has been extensively studied by chemical network calculation assuming chemical reaction on the surface of grains. Such surface reaction would have played important roles at the very early stage of disk evolution or low temperature outer region; however, thermal processes should have been the dominant reaction at later or high temperature (~above the melting point of water ice) regions. Those organics should have been incorporated into planetesimals that would be a precursor material of life.We have developed a protoplanetary disk evolution model by combining fluid dynamics and chemical change of organics with the molecular cloud origin. On the basis of calculation, we discuss the temporal and spatial change of organics within the inner region of the disk. The organics initially has a composition of cometary organics, which is assume not to change up to T~250K, becomes rich in C up to T~400K, and changed into almost pure C at T>500K. At the early stage of disk evolution (t<105 years), a significant fraction of refractory organics (enriched in C and depleted in H, O, and N) is present in the asteroid belt, and the primitive (max T< 250K) organics are distributed beyond several AU, whereas, the primitive organics reached at the inner edge of the asteroid belt. Primitive organics are not present at ~1AU through the disk evolution.The results strongly suggests that the Earth does not contain primitive organics if all the embryos that formed the Earth were derived within ~2AU. On the other hand, some fraction of organics in the asteroid belt would be primitive that retain primitive nature originated in the molecular cloud with heavy isotope enrichments. If the disk was heavy and the high temperature region extended to outer regions, organics supplied to the steroidal belt should be

  2. Nano-structure fabrication by using self-organizing properties of materials

    SciTech Connect

    Hayashi, T.; Maruno, T.; Ishii, Y.

    1994-12-31

    Self-organizing properties of materials can be used to fabricate well-ordered nanostructures on a large scale and also to develop new advanced materials. Three examples of self-organized nanostructures are described in this paper. A unidirectionally ordered metallo-phthalocyanine thin film was formed over the entire surface of a sapphire (1{bar 1}02) substrate by using a newly synthesized dibenzo[b,t] phthalocyaninato-Zn(II), which has a unique two-fold symmetrical molecular structure. A buried SiO{sub 2} layer with atomically abrupt Si/SiO{sub 2} interface was formed by oxygen ion implantation into silicon and subsequent annealing. A nano-particle consisting of outer graphitic shells and a core nano-crystal of LaC{sub 2} was formed in a self-organizing manner when a hot carbon-lanthanum particle was cooled on an arc-discharge electrode in a He atmosphere.

  3. Milk and serum standard reference materials for monitoring organic contaminants in human samples.

    PubMed

    Schantz, Michele M; Eppe, Gauthier; Focant, Jean-François; Hamilton, Coreen; Heckert, N Alan; Heltsley, Rebecca M; Hoover, Dale; Keller, Jennifer M; Leigh, Stefan D; Patterson, Donald G; Pintar, Adam L; Sharpless, Katherine E; Sjödin, Andreas; Turner, Wayman E; Vander Pol, Stacy S; Wise, Stephen A

    2013-02-01

    Four new Standard Reference Materials (SRMs) have been developed to assist in the quality assurance of chemical contaminant measurements required for human biomonitoring studies, SRM 1953 Organic Contaminants in Non-Fortified Human Milk, SRM 1954 Organic Contaminants in Fortified Human Milk, SRM 1957 Organic Contaminants in Non-Fortified Human Serum, and SRM 1958 Organic Contaminants in Fortified Human Serum. These materials were developed as part of a collaboration between the National Institute of Standards and Technology (NIST) and the Centers for Disease Control and Prevention (CDC) with both agencies contributing data used in the certification of mass fraction values for a wide range of organic contaminants including polychlorinated biphenyl (PCB) congeners, chlorinated pesticides, polybrominated diphenyl ether (PBDE) congeners, and polychlorinated dibenzo-p-dioxin (PCDD) and dibenzofuran (PCDF) congeners. The certified mass fractions of the organic contaminants in unfortified samples, SRM 1953 and SRM 1957, ranged from 12 ng/kg to 2200 ng/kg with the exception of 4,4'-DDE in SRM 1953 at 7400 ng/kg with expanded uncertainties generally <14 %. This agreement suggests that there were no significant biases existing among the multiple methods used for analysis. PMID:23132544

  4. Fumed silica nanoparticle mediated biomimicry for optimal cell-material interactions for artificial organ development.

    PubMed

    de Mel, Achala; Ramesh, Bala; Scurr, David J; Alexander, Morgan R; Hamilton, George; Birchall, Martin; Seifalian, Alexander M

    2014-03-01

    Replacement of irreversibly damaged organs due to chronic disease, with suitable tissue engineered implants is now a familiar area of interest to clinicians and multidisciplinary scientists. Ideal tissue engineering approaches require scaffolds to be tailor made to mimic physiological environments of interest with specific surface topographical and biological properties for optimal cell-material interactions. This study demonstrates a single-step procedure for inducing biomimicry in a novel nanocomposite base material scaffold, to re-create the extracellular matrix, which is required for stem cell integration and differentiation to mature cells. Fumed silica nanoparticle mediated procedure of scaffold functionalization, can be potentially adapted with multiple bioactive molecules to induce cellular biomimicry, in the development human organs. The proposed nanocomposite materials already in patients for number of implants, including world first synthetic trachea, tear ducts and vascular bypass graft. PMID:24243739

  5. Organic Materials Ionizing Radiation Susceptibility for the Outer Planet/Solar Probe Radioisotope Power Source

    NASA Technical Reports Server (NTRS)

    Golliher, Eric L.; Pepper, Stephen V.

    2001-01-01

    The Department of Energy is considering the current Stirling Technology Corporation 55 We Stirling Technology Demonstration Convertor as a baseline option for an advanced radioisotope power source for the Outer Planets/Solar Probe project of Jet Propulsion Laboratory and other missions. However, since the Technology Demonstration Convertor contains organic materials chosen without any special consideration of flight readiness, and without any consideration of the extremely high radiation environment of Europa, a preliminary investigation was performed to address the radiation susceptibility of the current organic materials used in the Technology Demonstration Convertor. This report documents the results of the investigation. The results of the investigation show that candidate replacement materials have been identified to be acceptable in the harsh Europa radiation environment.

  6. Light-Emitting Organic Materials with Variable Charge Injection and Transport Properties

    SciTech Connect

    Chen, A. C.-A.; Wallace, J. U.; Wei, S. K.-H.; Zeng, L.; Shen, S. H.; Blenton, T. N.

    2006-01-01

    Novel light-emitting organic materials comprising conjugated oligomers chemically attached via a flexible spacer to an electron- or hole-conducting core were designed for tunable charge injection and transport properties. Representative glassy-isentropic and glassy-liquid-crystalline (i.e., noncrystaline solid) materials were synthesized and characterized; they were found to exhibit a glass transition temperature and a clearing point close to 140 and 250 C, respectively; an orientational order parameter of 0.75; a photoluminescence quantum yield up to 51%; and HOMO and LUMO energy levels intermediate between those of blue-emitting oligofluorenes and the ITO and Mg/Ag electrodes commonly used in organic light-emitting diodes, OLEDs. This class of materials will help to balance charge injection and transport and to spread out the charge recombination zone, thereby significantly improving the device efficiency and lifetime of unpolarized and polarized OLEDs.

  7. Organic nanophotonic materials: the relationship between excited-state processes and photonic performances.

    PubMed

    Zhang, Wei; Zhao, Yong Sheng

    2016-07-12

    Nanophotonics have recently captured broad attention because of their great potential in information processing and communication, which may allow rates and bandwidth beyond what is feasible in the realm of electronics. Organic materials could be well suitable for such applications due to their ability to generate, transmit, modulate and detect light in their lightweight and flexible nanoarchitectures. Their distinct nanophotonic properties strongly depend on their extrinsic morphologies and intrinsic molecular excited-state processes. In this feature article, we mainly focus on a comprehensive understanding of the relationship between molecular excited-state processes and the advanced photonic functionalities of organic micro/nano-crystals in recent organic nanophotonic research, and then expect to provide enlightenment for the design and development of tiny photonic devices with broadband tunable properties by tailoring the excited-state processes of organic microcrystals. PMID:26883812

  8. Subdiffraction-resolution fluorescence microscopy reveals a domain of the centrosome critical for pericentriolar material organization.

    PubMed

    Mennella, V; Keszthelyi, B; McDonald, K L; Chhun, B; Kan, F; Rogers, G C; Huang, B; Agard, D A

    2012-11-01

    As the main microtubule-organizing centre in animal cells, the centrosome has a fundamental role in cell function. Surrounding the centrioles, the pericentriolar material (PCM) provides a dynamic platform for nucleating microtubules. Although the importance of the PCM is established, its amorphous electron-dense nature has made it refractory to structural investigation. By using SIM and STORM subdiffraction-resolution microscopies to visualize proteins critical for centrosome maturation, we demonstrate that the PCM is organized into two main structural domains: a layer juxtaposed to the centriole wall, and proteins extending farther away from the centriole organized in a matrix. Analysis of Pericentrin-like protein (PLP) reveals that its carboxy terminus is positioned at the centriole wall, it radiates outwards into the matrix and is organized in clusters having quasi-nine-fold symmetry. By RNA-mediated interference (RNAi), we show that PLP fibrils are required for interphase recruitment and proper mitotic assembly of the PCM matrix. PMID:23086239

  9. Charge Carrier Transport Through the Interface Between Hybrid Electrodes and Organic Materials in Flexible Organic Light Emitting Diodes.

    PubMed

    Zhou, Huanyu; Cheong, Hahn-Gil; Park, Jin-Woo

    2016-05-01

    We investigated the electronic properties of composite-type hybrid transparent conductive electrodes (h-TCEs) based on Ag nanowire networks (AgNWs) and indium tin oxide (ITO). These h-TCEs were developed to replace ITO, and their mechanical flexibility is superior to that of ITO. However, the characteristics of charge carriers and the mechanism of charge-carrier transport through the interface between the h-TCE and an organic material are not well understood when the h-TCE is used as the anode in a flexible organic light-emitting diode (f-OLED). AgNWs were spin coated onto polymer substrates, and ITO was sputtered atop the AgNWs. The electronic energy structures of h-TCEs were investigated by ultraviolet photoelectron spectroscopy. f-OLEDs were fabricated on both h-TCEs and ITO for comparison. The chemical bond formation at the interface between the h-TCE and the organic layer in f-OLEDs was investigated by X-ray photoelectron spectroscopy. The performances of f-OLEDs were compared based on the analysis results. PMID:27483896

  10. Impact of materials used in lab and field experiments on the recovery of organic micropollutants

    NASA Astrophysics Data System (ADS)

    Hebig, Klaus; Nödler, Karsten; Licha, Tobias; Scheytt, Traugott

    2015-04-01

    Organic micropollutants are frequently detected in the aquatic environment. There-fore, a large number of field and laboratory studies have been conducted in order to study their fate in the environment. Due to the diversity of chemical properties among these compounds some of them may interact with materials commonly used in field and laboratory studies like tubes, filters, or sample bottles. The aim of our experiment was to study the interaction between those materials and an aqueous solution of 43 widely detected basic, neutral, and acidic organic micropollutants hereby covering a broad range of polarities. Experiments with materials were conducted as a batch study using spiked tap water and for different syringe filters by filtration with subsequent fraction collection. The best recoveries over a wide range of organic compounds were observed for batches in contact with the following materials (in descending order) acryl glass, PTFE, HDPE, and PP. The use of Pharmed©, silicone, NBR70, Tygon©, and LDPE should be avoided. Flexible tubing materials especially influence many of the investigated compounds here. Filtration with most of the tested filter types leads to no significant loss of almost all of the investigated micropollutants. Nonetheless, significant mass losses of some compounds (loratadine, fluoxetine, sertraline, and diuron) were observed during the first mL of the filtration process. No systematic correlation between compound properties, tested materials, and ob-served mass losses could be identified in this study. The behavior of each compound is specific and thus, not predictable. It is therefore suggested to study the interaction of compounds with filters and material prior to the actual experiment or include blank studies.

  11. Impact of materials used in lab and field experiments on the recovery of organic micropollutants.

    PubMed

    Hebig, Klaus H; Nödler, Karsten; Licha, Tobias; Scheytt, Traugott J

    2014-03-01

    Organic micropollutants are frequently detected in the aquatic environment. Therefore, a large number of field and laboratory studies have been conducted in order to study their fate in the environment. Due to the diversity of chemical properties among these compounds some of them may interact with materials commonly used in field and laboratory studies like tubes, filters, or sample bottles. The aim of our experiment was to study the interaction between those materials and an aqueous solution of 43 widely detected basic, neutral, and acidic organic micropollutants hereby covering a broad range of polarities. Experiments with materials were conducted as a batch study using spiked tap water and for different syringe filters by filtration with subsequent fraction collection. The best recoveries over a wide range of organic compounds were observed for batches in contact with the following materials (in descending order) acryl glass, PTFE, HDPE, and PP. The use of Pharmed©, silicone, NBR70, Tygon©, and LDPE should be avoided. Flexible tubing materials especially influence many of the investigated compounds here. Filtration with most of the tested filter types leads to no significant loss of almost all of the investigated micropollutants. Nonetheless, significant mass losses of some compounds (loratadine, fluoxetine, sertraline, and diuron) were observed during the first mL of the filtration process. No systematic correlation between compound properties, tested materials, and observed mass losses could be identified in this study. The behavior of each compound is specific and thus, not predictable. It is therefore suggested to study the interaction of compounds with filters and material prior to the actual experiment or include blank studies. PMID:24365588

  12. Single crystal films and waveguides of organic materials: Preparation and nonlinear optical properties

    NASA Astrophysics Data System (ADS)

    Thakur, Mrinal

    1994-03-01

    The objective of this program is to establish a generic method for the growth of thin single crystal films of important organic nonlinear optical materials and measurement of their nonlinear optical properties. Through the last year's effort we have successfully prepared single crystal films of three organic materials which are: (1) (N-(4-Nitrophenyl)-L-prolinol) abbreviated as NPP, (2) 2-cyclooctylamino- 5-nitropyridine, abbreviated as COANP, and (3) 4'-N, N-dimethylamino- 4-N-methylstilbazolium toluene-p-sulfonate, abbreviated as DAST. These materials have very large second order susceptibilities. Both NPP and COANP have an amphiphillic molecular structure, while DAST is an organic molecular salt. The single crystal films were prepared by a method called the shear method, with appropriate choice of the growth conditions. The shear method involves crystal growth at an interface and was originally applied to the growth of polydiacetylene films. Our results show that using the principles involved in the shear method, if the growth conditions are properly optimized for each compound, then molecules other than diacetylene are possible to organize as single crystal films. The only major condition that needs to be satisfied for this method to be applicable is that the molecule must be of an elongated shape with polar chemical groups at one or both ends.

  13. Processing of organic electro-optic materials: solution-phase assisted reorientation of chromophores

    NASA Astrophysics Data System (ADS)

    Olbricht, Benjamin C.; Eng, David L. K.; Kozacik, Stephen T.; Ross, Dylan; Prather, Dennis W.

    2013-03-01

    Organic EO materials, sometimes called EO polymers, offer a variety of very promising properties that have improved at remarkable rates over the last decade, and will continue to improve. However, these materials rely on a "poling" process to afford EO activity, which is commonly cited as the bottleneck for the widespread implementation of organic EO material-containing devices. The Solution Phase-Assisted Reorientation of Chromophores (SPARC) is a process that utilizes the mobility of chromophores in the solution phase to afford acentric molecular order during deposition. The electric field can be generated by a corona discharge in a carefully-controlled gas environment. The absence of a poling director during conventional spin deposition forms centric pairs of chromophores which may compromise the efficacy of thermal poling. Direct spectroscopic evidence of linear dichroism in modern organic EO materials has estimated the poling-induced order of the chromophores to be 10-15% of its theoretical maximum, offering the potential for a manyfold enhancement in EO activity if poling is improved. SPARC is designed to overcome these limitations and also to allow the poling of polymeric hosts with temporal thermal (alignment) stabilities greater than the decomposition temperature of the guest chromophore. In this report evidence supporting the theory motivating the SPARC process and the resulting EO activities will be presented. Additionally, the results of trials towards a device demonstration of the SPARC process will be discussed.

  14. Reaction mechanisms of oxygen plasma interaction with organosilicate low-k materials containing organic crosslinking groups

    SciTech Connect

    Chaudhari, Mrunalkumar; Du Jincheng

    2012-11-15

    Integration of low dielectric constant (k) materials such as organosilicate glasses (OSG) into microelectronic processing demands a better of understanding the plasma/OSG interactions during plasma etching and ashing of these materials, based on which low-k materials with higher radiation resistance and better mechanical behaviors can be developed and optimized plasma processing conditions can be introduced to ensure continued miniaturization of semiconductor devices. Introducing organic crosslinking (e.g., -CH{sub 2}-) in OSG has been shown to be an effective measure to improve the mechanical properties but their effect on plasma interaction is still not fully understood. In this paper, ab initio based molecular dynamics simulations have been employed to investigate the effect of the oxygen plasma on the carbon-bridged silicate networks in the OSG material. The results show that organic crosslinking in the Si-O-Si network leads to lower energy reaction pathways with atomic oxygen radicals that result in breakage of Si-CH{sub 2}-Si linkages instead of Si-CH{sub 3} bonds and, consequently, a decrease in carbon removal. The incorporation of organic crosslinking groups can thus improve the resistance to oxygen plasma damage of OSG and, together with better mechanical properties, can lead to the design of stronger low-k dielectric films.

  15. Next generation organic light-emitting materials and devices (Presentation Recording)

    NASA Astrophysics Data System (ADS)

    Kippelen, Bernard

    2015-10-01

    In this talk, we will discuss recent innovations in organic light-emitting materials and devices. First, we will report on organic light-emitting diodes (OLEDs) based on thermally activated delayed fluorescence (TADF). We will show that devices based on the emitter 4CzIPN doped in a novel ambipolar host can yield a current efficacy of 81 cd/A and a maximum external quantum efficiency of 26.5%. These devices exhibit a low turn-on voltage of 3.2 V at 10 cd/m2, as well as reduced efficiency roll-off at high current densities. The performance of these devices is comparable to that of electrophosphorescent devices based on organic-metallic compounds that contain precious metals such as Iridium. In a second part we will report on highly efficient green-emitting organic light-emitting diodes (OLEDs) fabricated on shape memory polymer (SMP) substrates for flexible electronic applications. SMPs are a class of mechanically active materials that can change and store shape upon activation by a stimulus. The combination of the unique properties of SMP substrates with the light-emitting properties of OLEDs pave to the way for new applications, including conformable smart skin devices, minimally invasive biomedical devices, and flexible lighting/display technologies. Finally, we will present OLEDs fabricated on substrates made from cellulose nanocrystals (CNC) and discuss how such substrates can reduce the environmental footprint of printable organic electronics.

  16. Conversion of organic material by black soldier fly larvae: establishing optimal feeding rates.

    PubMed

    Diener, Stefan; Zurbrügg, Christian; Tockner, Klement

    2009-09-01

    Larvae of the black soldier fly, Hermetia illucens (Diptera: Stratiomyidae), are voracious feeders of organic material and may thus be used in simple engineered systems to reduce organic waste in low- and middle-income countries. Controlled feeding experiments with standard fodder were conducted to assess the optimum amount of organic waste to be added to a CORS system (Conversion of Organic Refuse by Saprophages). A daily feeding rate of 100 mg chicken feed (60% moisture content) per larva resulted in an optimum trade-off between material reduction efficiency (41.8%, SE 0.61) and biomass production (prepupal dry weight: 48.0 mg, SE 2.0). Applied to market waste and human faeces, this corresponds to a potential daily feeding capacity of 3-5 kg/m(2) and 6.5 kg/m(2), respectively. In addition, H. illucens prepupae quality was assessed to determine their suitability to substitute fishmeal in animal feed production. The chitin-corrected crude protein content ranged from 28.2 to 42.5%, depending on the amount of food provided to the larvae. Based on our study, a waste processing unit could yield a daily prepupal biomass of 145 g (dry mass) per m(2). We conclude that larvae of the black soldier fly are potentially capable of converting large amounts of organic waste into protein-rich biomass to substitute fishmeal, thereby contributing to sustainable aquaculture. PMID:19502252

  17. Material properties and field-effect transistor characteristics of hybrid organic/graphene active layers

    NASA Astrophysics Data System (ADS)

    Ha, Tae-Jun; Lee, Jongho; Chowdhury, Sk. Fahad; Akinwande, Deji; Dodabalapur, Ananth

    2012-10-01

    We report on the material properties and device characteristics of field-effect transistors (FETs) consisting of hybrid mono-layer graphene/organic semiconductor active layers. By capping with selected organic and polymeric layers, transformation of the electronic characteristics of mono-layer graphene FETs was observed. The off-state current is reduced while the on-state current and field-effect mobility are either unaffected or increased after depositing π-conjugated organic semiconductors. Significantly, capping mono-layer graphene FETs with fluoropolymer improved the on-off current ratio from 5 to 10 as well as increased the field-effect mobility by factor of two compared to plain graphene FETs. Removal of π-conjugated organic semiconductors or fluoropolymer from graphene FETs results in a return to the original electronic properties of mono-layer graphene FETs. This suggests that weak reversible electronic interactions between graphene and π-conjugated organic semiconductors/fluoropolymer favorably tune the material and electrical characteristics of mono-layer graphene.

  18. Extraction of Organic Molecules from Terrestrial Material: Quantitative Yields from Heat and Water Extractions

    NASA Technical Reports Server (NTRS)

    Beegle, L. W.; Abbey, W. A.; Tsapin, A. T.; Dragoi, D.; Kanik, I.

    2004-01-01

    In the robotic search for life on Mars, different proposed missions will analyze the chemical and biological signatures of life using different platforms. The analysis of samples via analytical instrumentation on the surface of Mars has thus far only been attempted by the two Viking missions. Robotic arms scooped relogith material into a pyrolysis oven attached to a GC/MS. No trace of organic material was found on any of the two different samples at either of the two different landing sites. This null result puts an upper limit on the amount of organics that might be present in Martian soil/rocks, although the level of detection for each individual molecular species is still debated. Determining the absolute limit of detection for each analytical instrument is essential so that null results can be understood. This includes investigating the trade off of using pyrolysis versus liquid solvent extraction to release organic materials (in terms of extraction efficiencies and the complexity of the sample extraction process.) Extraction of organics from field samples can be accomplished by a variety of methods such utilizing various solvents including HCl, pure water, supercritical fluid and Soxhelt extraction. Utilizing 6N HCl is one of the most commonly used method and frequently utilized for extraction of organics from meteorites but it is probably infeasible for robotic exploration due to difficulty of storage and transport. Extraction utilizing H2O is promising, but it could be less efficient than 6N HCl. Both supercritical fluid and Soxhelt extraction methods require bulky hardware and require complex steps, inappropriate for inclusion on rover spacecraft. This investigation reports the efficiencies of pyrolysis and solvent extraction methods for amino acids for different terrestrial samples. The samples studied here, initially created in aqueous environments, are sedimentary in nature. These particular samples were chosen because they possibly represent one of the

  19. Material degradation of liquid organic semiconductors analyzed by nuclear magnetic resonance spectroscopy

    SciTech Connect

    Fukushima, Tatsuya; Yamamoto, Junichi; Fukuchi, Masashi; Kaji, Hironori; Hirata, Shuzo; Jung, Heo Hyo; Adachi, Chihaya; Hirata, Osamu; Shibano, Yuki

    2015-08-15

    Liquid organic light-emitting diodes (liquid OLEDs) are unique devices consisting only of liquid organic semiconductors in the active layer, and the device performances have been investigated recently. However, the device degradation, especially, the origin has been unknown. In this study, we show that material degradation occurs in liquid OLEDs, whose active layer is composed of carbazole with an ethylene glycol chain. Nuclear magnetic resonance (NMR) experiments clearly exhibit that the dimerization reaction of carbazole moiety occurs in the liquid OLEDs during driving the devices. In contrast, cleavages of the ethylene glycol chain are not detected within experimental error. The dimerization reaction is considered to be related to the device degradation.

  20. Metal-organic frameworks as host materials of confined supercooled liquids

    NASA Astrophysics Data System (ADS)

    Fischer, J. K. H.; Sippel, P.; Denysenko, D.; Lunkenheimer, P.; Volkmer, D.; Loidl, A.

    2015-10-01

    In this work, we examine the use of metal-organic framework (MOF) systems as host materials for the investigation of glassy dynamics in confined geometry. We investigate the confinement of the molecular glass former glycerol in three MFU-type MOFs with different pore sizes (MFU stands for "Metal-Organic Framework Ulm-University") and study the dynamics of the confined liquid via dielectric spectroscopy. In accord with previous reports on confined glass formers, we find different degrees of deviations from bulk behavior depending on pore size, demonstrating that MOFs are well-suited host systems for confinement investigations.

  1. Remotely operated organic liquid waste incinerator for the fuels and materials examination facility

    SciTech Connect

    Sales, W.L.; Barker, R.E.; Hershey, R.B.

    1980-01-01

    The search for a practical method for the disposal of small quantities of oraganic liquid waste, a waste product of metallographic sample preparation at the Fuels and Materials Examination Facility has led to the design of an incinerator/off-gas system to burn organic liquid wastes and selected organic solids. The incinerator is to be installed in a shielded inert-atmosphere cell, and will be remotely operated and maintained. The off-gas system is a wet-scrubber and filter system designed to release particulate-free off-gas to the FMEF Building Exhaust System.

  2. Sorption Characteristics of Organic Powder Sorption Material in Fluidized Bed with a Cooling Pipe

    NASA Astrophysics Data System (ADS)

    Horibe, Akihiko; Husain, Syahrul; Inaba, Hideo; Haruki, Naoto

    The dynamic sorption characteristics of organic sorbent materials have been studied by using fluidized bed with a cooling pipe. The organic powder type sorbent made from a bridged complex of sodium polyacrylate which is one of the sorption polymers is adopted in this study. Sorption rate of water vapor and the variation of temperature in the sorbent bed with time were measured under various conditions. As a result, sorption ratio increases and the completion time for the sorption process decreases by using a cooling pipe. Furthermore, the non-dimensional correlation equations were obtained for water vapor mass transfer under sorption process in terms of relevant non-dimensional parameters.

  3. Effect of experimental crude oil contamination on abundance, mortality and resettlement of representative mud flat organisms in the mesohaline area of the elbe estuary

    NASA Astrophysics Data System (ADS)

    Van Bernem, K. H.

    After repeated experimental contamination with small doses of the crude oils Arabian light, Kuwait crude and Iranian light on a silty mud flat in the Elbe estuary, neither an increased mortality nor emigration was found in Macoma balthica or Nereis diversicolor. Oligochaetes increased in abundance. The entire population of Corophium volutator tried to leave the contaminated sediment. Most specimens came into contact with the oil coating of the sediment and were killed. Twelve weeks after the beginning of the contaminations the original community structure had reestablished. Different effects between the 3 crude oils tested were not significant.

  4. Characterization of dissolved organic materials in surface waters within the blast zone of Mount St Helens, Washington

    USGS Publications Warehouse

    McKnight, Diane M.; Pereira, W.E.; Ceazan, M.L.; Wissmar, Robert C.

    1982-01-01

    After the May 18, 1980, eruption of Mount St Helens, the concentration of dissolved organic material in surface waters near the volcano increased significantly as a result of the destruction of the surrounding conifer forest. Low molecular weight organic compounds identified in the blast zone surface waters were derived from pyrolysis of plant and soil organic materials incorporated into pyroclastic flow, mud flow and debris avalanche deposits. A major fraction of the dissolved organic material consisted of high molecular weight, colored, organic acids that are similar in their general properties to aquatic fulvic acids found in more typical surface waters except for greater sulfur contents. The other major fraction of the dissolved organic material consisted of hydrophilic acids, which may include compounds capable of supporting heterotrophic microorganisms, and precursors in the formation of aquatic fulvic acids. The organic chemistry of blast zone surface waters will probably be greatly influenced by the May 18, 1980, eruption for many years. ?? 1982.

  5. Zirconia-based luminescent organic-inorganic hybrid materials with ternary europium (III) complexes bonded

    NASA Astrophysics Data System (ADS)

    Yang, Jing; Li, Zhiqiang; Xu, Yang; Wang, Yige

    2016-05-01

    In this work, a novel red-emitting organic-inorganic hybrid material with europium (III) lanthanide β-diketonate complexes linked to a zirconia was reported, which was realized by adduct formation with zirconia-tethered terpyridine moieties. Luminescence enhancement of the hybrid material has been observed compared with pure Eu(tta)3·2H2O. Transparent and strongly luminescent thin films based on PMMA were also prepared at room temperature, which are highly luminescent under UV-light irradiation and possess a promising prospect in the area of optics.

  6. Application of micro-scale thermography to the thermal analysis of polymeric and organic materials

    NASA Astrophysics Data System (ADS)

    Morikawa, Junko; Hayakawa, Eita; Hashimoto, Toshimasa

    2011-05-01

    The applications of uncooled micro-bolometer VOx FPA to the micro-scale thermal analysis of polymeric & organic materials are presented. The latent heat during phase transition is analyzed with the emissivity correction calculation for all pixels that include the calibration algorithm using a real time direct impose signal system. It enables to visualize the exothermic latent heat of freezing biological cells at minus temperature. In comparison with the previously obtained data by using the InSb FPA sensor, the limitation and the possibility of the un-cooled micro-bolometer in view of application in thermal analysis of materials characterization are discussed.

  7. Smart Organic Two-Dimensional Materials Based on a Rational Combination of Non-covalent Interactions.

    PubMed

    Bai, Wei; Jiang, Ziwen; Ribbe, Alexander E; Thayumanavan, S

    2016-08-26

    Rational design of organic 2D (O2D) materials has made some progress, but it is still in its infancy. A class of self-assembling small molecules is presented that form nano/microscale supramolecular 2D materials in aqueous media. A judicial combination of four different intermolecular interactions forms the basis for the robust formation of these ultrathin assemblies. These assemblies can be programmed to disassemble in response to a specific protein and release its non-covalently bound guest molecules. PMID:27490155

  8. Self-organization of dissipationless solitons in positive- and negative-refractive-index materials

    SciTech Connect

    Skarka, V.; Aleksic, N. B.; Berezhiani, V. I.

    2010-04-15

    A generalized Ginzburg-Landau equation describing dissipative solitons dynamics in negative-refractive-index materials is derived from Maxwell equations. This equation having only real terms with opposite sign differs from the usual Ginzburg-Landau equation for positive-refractive-index media. A cross-compensation between the saturating nonlinearity excess, losses, and gain makes obtained self-organized solitons dissipationless and exceptionally robust. In the presence of such solitons medium becomes effectively dissipationless. The compensation of losses is of particular interest for media with resonant character of interactions like negative-refractive-index materials.

  9. Carbon dioxide capturing technologies: a review focusing on metal organic framework materials (MOFs).

    PubMed

    Sabouni, Rana; Kazemian, Hossein; Rohani, Sohrab

    2014-04-01

    In this study, a relevant literature has been reviewed focusing on the carbon dioxide capture technologies in general, such as amine-based absorption as conventional carbon dioxide capturing technology, aqueous ammonia-based absorption, membranes, and adsorption material (e.g., zeolites, and activated carbons). In more details, metal organic frameworks (MOFs) as new emerging technologies for carbon dioxide adsorption are discussed. The MOFs section is intended to provide a comprehensive overview of MOFs including material characteristics and synthesis, structural features, CO2 adsorption capacity, heat of adsorption and selectivity of CO2. PMID:24338107

  10. Benzophenones as Generic Host Materials for Phosphorescent Organic Light-Emitting Diodes.

    PubMed

    Jhulki, Samik; Seth, Saona; Ghosh, Avijit; Chow, Tahsin J; Moorthy, Jarugu Narasimha

    2016-01-20

    Despite the fact that benzophenone has traditionally served as a prototype molecular system for establishing triplet state chemistry, materials based on molecular systems containing the benzophenone moiety as an integral part have not been exploited as generic host materials in phosphorescent organic light-emitting diodes (PhOLEDs). We have designed and synthesized three novel host materials, i.e., BP2-BP4, which contain benzophenone as the active triplet sensitizing molecular component. It is shown that their high band gap (3.91-3.93 eV) as well as triplet energies (2.95-2.97 eV) permit their applicability as universal host materials for blue, green, yellow, and red phosphors. While they serve reasonably well for all types of dopants, excellent performance characteristics observed for yellow and green devices are indeed the hallmark of benzophenone-based host materials. For example, maximum external quantum efficiencies of the order of 19.2% and 17.0% were obtained from the devices fabricated with yellow and green phosphors using BP2 as the host material. White light emission, albeit with rather poor efficiencies, has been demonstrated as a proof-of-concept by fabrication of co-doped and stacked devices with blue and yellow phosphors using BP2 as the host material. PMID:26690799

  11. Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials.

    PubMed

    Blair, L H; Colakel, A; Vrcelj, R M; Sinclair, I; Coles, S J

    2015-08-01

    A new approach to formulating pyrotechnic materials is presented whereby constituent ingredients are bound together in a solid-state lattice. This reduces the batch inconsistencies arising from the traditional approach of combining powders by ensuring the key ingredients are 'mixed' in appropriate quantities and are in intimate contact. Further benefits of these types of material are increased safety levels as well as simpler logistics, storage and manufacture. A systematic series of new frameworks comprising fuel and oxidiser agents (group 1 and 2 metal nodes & terephthalic acid derivatives as linkers) has been synthesised and structurally characterised. These new materials have been assessed for pyrotechnic effect by calorimetry and burn tests. Results indicate that these materials exhibit the desired pyrotechnic material properties and the effect can be correlated to the dimensionality of the structure. A new approach to formulating pyrotechnic materials is proposed whereby constituent ingredients are bound together in a solid-state lattice. A series of Metal-organic framework frameworks comprising fuel and oxidiser agents exhibits the desired properties of a pyrotechnic material and this effect is correlated to the dimensionality of the structure. PMID:26138789

  12. An Investigation into the Physico-chemical Factors Affecting the Abundance and Diversity of Aquatic Insects in Organically Manured Aquadams and Their Utilization by Oreochromis mossambicus (Perciformes: Cichlidae).

    PubMed

    Rapatsa, M M; Moyo, N A G

    2015-08-01

    The interaction between the fish Oreochromis mossambicus (Percifomes: Cichlidae) and aquatic insects after application of chicken, cow, and pig manure was studied in 7,000-liter plastic aquadams. Principal component analysis showed that most of the variation in water quality after application of manure was accounted for by potassium, nitrogen, dissolved oxygen, phosphate, and alkalinity. Canonical correspondence analysis showed that Gyrinidae, Elminidae, Hydrophilidae, Hydraenidae, and Athericidae were associated with high nutrient levels (nitrogen, phosphorus, and potassium) characteristic of the chicken manure. However, the most abundant aquatic insects Gerridae, Notonectidae, and Culicidae were close to the centre of the ordination and not defined by any nutrient gradient. The Shannon-Wiener diversity was highest in the aquadams treated with chicken manure. The most frequently occurring aquatic insects in the diet of O. mossambicus were culicid mosquitoes in all the treatments. However, in the laboratory, Chironomidae were the most preferred because they lacked refuge. Notonectidae and Gerridae were not recorded in the diet of O. mossambicus despite their abundance. This may be because of their anti-predation strategies. Laboratory experiments showed that Notonectidae, Gyrinidae, and Gerridae fed on Chironomidae and Culicidae. This implies that aquatic predatory insects competed for food with O. mossambicus. PMID:26314044

  13. First discovery of the organic materials in deep-sea iron cosmic spherule

    NASA Technical Reports Server (NTRS)

    Hanchang, Peng; Peicang, XU

    1993-01-01

    The dust impact mass analyzer (PUMA) carried by the spacecraft Vega 1, Vega 2 and Giotto has provided the first direct measurements of the physical and chemical properties of cometary dust. The results indicate that most of the cometary dust particles are rich in light elements such as H, C, N, and O, suggesting the validity of models that describe the cometary dust as including organic material. Up to now, there were none found with the organic material from the deep-sea cosmic spherules. We have determined this from the deep-sea iron cosmic spherules collected from the North Pacific. An iron cosmic spherule (382 microns in diameter) was determined by the Laser Raman Microprobe.

  14. Quantum spin Hall and Z2 metallic states in an organic material

    NASA Astrophysics Data System (ADS)

    Zhao, Bao; Zhang, Jiayong; Feng, Wanxiang; Yao, Yugui; Yang, Zhongqin

    2014-11-01

    Motivated by recently searching for topological states in organic materials as well as successful experimental synthesis of a graphitelike metal-organic framework Ni3(C18H12N6 )2 [Sheberla et al., J. Am. Chem. Soc. 136, 8859 (2014), 10.1021/ja502765n], we systematically investigated the electronic and topological properties of the Ni3(C18H12N6 )2 monolayer using an ab initio method combined with a tight-binding model. Our calculations demonstrate that the material can be in a quantum spin Hall or Z2 metallic state in different electron-doped concentrations, which are experimentally accessible with currently electrostatic gating technologies. The tight-binding model also shows that the real next-nearest-neighbor interaction is essential to drive the Z2 metallic phase in Ni3(C18H12N6 )2-type lattices.

  15. Suppressing molecular motions for enhanced room-temperature phosphorescence of metal-free organic materials

    PubMed Central

    Kwon, Min Sang; Yu, Youngchang; Coburn, Caleb; Phillips, Andrew W.; Chung, Kyeongwoon; Shanker, Apoorv; Jung, Jaehun; Kim, Gunho; Pipe, Kevin; Forrest, Stephen R.; Youk, Ji Ho; Gierschner, Johannes; Kim, Jinsang

    2015-01-01

    Metal-free organic phosphorescent materials are attractive alternatives to the predominantly used organometallic phosphors but are generally dimmer and are relatively rare, as, without heavy-metal atoms, spin–orbit coupling is less efficient and phosphorescence usually cannot compete with radiationless relaxation processes. Here we present a general design rule and a method to effectively reduce radiationless transitions and hence greatly enhance phosphorescence efficiency of metal-free organic materials in a variety of amorphous polymer matrices, based on the restriction of molecular motions in the proximity of embedded phosphors. Covalent cross-linking between phosphors and polymer matrices via Diels–Alder click chemistry is devised as a method. A sharp increase in phosphorescence quantum efficiency is observed in a variety of polymer matrices with this method, which is ca. two to five times higher than that of phosphor-doped polymer systems having no such covalent linkage. PMID:26626796

  16. Photochromic organic-inorganic composite materials prepared by sol-gel processing: Properties and potentials

    SciTech Connect

    Hou, L. |; Mennig, M.; Schmidt, H.

    1994-12-31

    The sol-gel method which features a low-temperature wet-chemical process opens vast possibilities to incorporating organic dyes into solid matrices for various optical applications. In this paper the authors present their experimental results on the sol-gel derived photochromic organic-inorganic composite (Ormocer) materials following an introductory description of the sol-gel process and a brief review on the state of the art of the photochromic solids prepared using this method. Their photochromic spirooxazine-Ormocer gels and coatings possess better photochromic response and color-change speed than the corresponding photochromic polymer coatings and similar photochemical stability to the latter. Further developments are proposed as to tackle the temperature dependence problem and further tap the potentialities of the photochromic dye-Ormocer material for practical applications.

  17. Dependence on material choice of degradation of organic solar cells following exposure to humid air

    PubMed Central

    Glen, Tom S.; Scarratt, Nicholas W.; Yi, Hunan; Iraqi, Ahmed; Wang, Tao; Kingsley, James; Buckley, Alastair R.; Lidzey, David G.

    2015-01-01

    ABSTRACT Electron microscopy has been used to study the degradation of organic solar cells when exposed to humid air. Devices with various different combinations of commonly used organic solar cell hole transport layers and cathode materials have been investigated. In this way the ingress of water and the effect it has on devices could be studied. It was found that calcium and aluminum in the cathode both react with water, causing voids and delamination within the device. The use of poly(3,4‐ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) was found to increase the degradation by easing water ingress into the device. Replacing these materials removed these degradation features. © 2015 The Authors. Journal of Polymer Science Part B: Polymer Physics published by Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016, 54, 216–224 PMID:27594763

  18. Interfacial Charge Transport in Organic Electronic Materials: the Key to a New Electronics Technology

    SciTech Connect

    Smith, D.L.; Campbell, I.H.; Davids, P.S.; Heller, C.M.; Laurich, B.K.; Crone, B.K.; Saxena, A.; Bishop, A.R.; Ferraris, J.P.; Yu, Z.G.

    1999-06-04

    This is the final report of a three-year, Laboratory Directed Research and Development (LDRD) project at Los Alamos National Laboratory (LANL). The primary aim of this project is to obtain a basic scientific understanding of electrical transport processes at interfaces that contain an organic electronic material. Because of their processing advantages and the tunability of their electronic properties, organic electronic materials are revolutionizing major technological areas such as information display. We completed an investigation of the fundamental electronic excitation energies in the prototype conjugated polymer MEH-PPV. We completed a combined theoretical/experimental study of the energy relation between charged excitations in a conjugated polymer and the metal at a polymer/metal interface. We developed a theoretical model that explains injection currents at polymer/metal interfaces. We have made electrical measurements on devices fabricated using the conjugated polymer MEH-PPV a nd a series of metals.

  19. Suppressing molecular motions for enhanced room-temperature phosphorescence of metal-free organic materials.

    PubMed

    Kwon, Min Sang; Yu, Youngchang; Coburn, Caleb; Phillips, Andrew W; Chung, Kyeongwoon; Shanker, Apoorv; Jung, Jaehun; Kim, Gunho; Pipe, Kevin; Forrest, Stephen R; Youk, Ji Ho; Gierschner, Johannes; Kim, Jinsang

    2015-01-01

    Metal-free organic phosphorescent materials are attractive alternatives to the predominantly used organometallic phosphors but are generally dimmer and are relatively rare, as, without heavy-metal atoms, spin-orbit coupling is less efficient and phosphorescence usually cannot compete with radiationless relaxation processes. Here we present a general design rule and a method to effectively reduce radiationless transitions and hence greatly enhance phosphorescence efficiency of metal-free organic materials in a variety of amorphous polymer matrices, based on the restriction of molecular motions in the proximity of embedded phosphors. Covalent cross-linking between phosphors and polymer matrices via Diels-Alder click chemistry is devised as a method. A sharp increase in phosphorescence quantum efficiency is observed in a variety of polymer matrices with this method, which is ca. two to five times higher than that of phosphor-doped polymer systems having no such covalent linkage. PMID:26626796

  20. Methods of chemical analysis for organic waste constituents in radioactive materials: A literature review

    SciTech Connect

    Clauss, S.A.; Bean, R.M.

    1993-02-01

    Most of the waste generated during the production of defense materials at Hanford is presently stored in 177 underground tanks. Because of the many waste treatment processes used at Hanford, the operations conducted to move and consolidate the waste, and the long-term storage conditions at elevated temperatures and radiolytic conditions, little is known about most of the organic constituents in the tanks. Organics are a factor in the production of hydrogen from storage tank 101-SY and represent an unresolved safety question in the case of tanks containing high organic carbon content. In preparation for activities that will lead to the characterization of organic components in Hanford waste storage tanks, a thorough search of the literature has been conducted to identify those procedures that have been found useful for identifying and quantifying organic components in radioactive matrices. The information is to be used in the planning of method development activities needed to characterize the organics in tank wastes and will prevent duplication of effort in the development of needed methods.

  1. Reactive Uptake of Ammonia and Formation of Organic Nitrogen Species for Non-Liquid/Liquid Secondary Organic Material

    NASA Astrophysics Data System (ADS)

    Martin, S. T.; Li, Y.; Liu, P.

    2015-12-01

    Formation of ammonium and organic nitrogen (ON) species was studied for secondary organic material (SOM) of variable viscosity, ranging from non-liquid to liquid physical states. The SOM was produced as particles of 50 to 150 nm in diameter in aerosol form from six precursors, including three terpenoid and three aromatic species. The viscosity of the hygroscopic SOM was adjusted by exposure to relative humidity (RH) from <5% to >90% RH in steps of 10% at 293 ± 2 K. The aerosol was subsequently exposed to 5 ppm NH3 for mean reaction times of 30, 370, or 5230 s. Ammonium and ON were characterized by high-resolution time-of-flight aerosol mass spectrometry (HR-ToF-AMS). The ammonium-to-organic ratio of mass concentrations (MNH4/MOrg) in the particles increased monotonically from <5% RH to a limiting value at a threshold RH, implicating a switchover in the reaction kinetics from a system limited by diffusivity within the SOM for low RH to one limited by other factors, such as saturated uptake, at higher RH. Formation of ON was observed for aromatic-derived SOMs, but not significant for terpenoid-derived SOMs. For aromatic-derived SOMs, the ON-to-organic ratio of mass concentrations (MON/MOrg) was negligible for RH <20%, increased monotonically from 20% to 60% RH, and stayed constant for RH >60%. The threshold RH for the switchover from kinetically controlled regime to a non-kinetically-controlled one was thus different between formation of ammonium and ON. This difference suggests that water may play a role in the slow reactions of ON formation as a reactant or a catalyst, in addition to affecting the reactant diffusion as in the fast reaction of ammonium formation. The implication is that formation of ammonium salts and organic nitrogen species by certain SOMs should be treated separately in chemical transport models to reflect the different roles of water that may affect the phase state of the SOMs or may act as a reactant or a catalyst.

  2. Metal-organic frameworks as cathode materials for Li-O2 batteries.

    PubMed

    Wu, Doufeng; Guo, Ziyang; Yin, Xinbo; Pang, Qingqing; Tu, Binbin; Zhang, Lijuan; Wang, Yong-Gang; Li, Qiaowei

    2014-05-28

    Metal-organic frameworks (MOFs) with open metal sites enrich the population of O2 in the pores significantly and assist the Li-O2 reaction when employed as a cell electrode material. A primary capacity of 9420 mA h g(-1) is achieved in a cell with Mn-MOF-74; more than four times higher than the value obtained in a cell without an MOF. PMID:24616022

  3. Development and Utilization of Host Materials for White Phosphorescent Organic Light-Emitting Diodes

    SciTech Connect

    Tang, Ching; Chen, Shaw

    2013-05-31

    Our project was primarily focused on the MYPP 2015 goal for white phosphorescent organic devices (PhOLEDs or phosphorescent organic light-emitting diodes) for solid-state lighting with long lifetimes and high efficiencies. Our central activity was to synthesize and evaluate a new class of host materials for blue phosphors in the PhOLEDs, known to be a weak link in the device operating lifetime. The work was a collaborative effort between three groups, one primarily responsible for chemical design and characterization (Chen), one primarily responsible for device development (Tang) and one primarily responsible for mechanistic studies and degradation analysis (Rothberg). The host materials were designed with a novel architecture that chemically links groups with good ability to move electrons with those having good ability to move “holes” (positive charges), the main premise being that we could suppress the instability associated with physical separation and crystallization of the electron conducting and hole conducting materials that might cause the devices to fail. We found that these materials do prevent crystallization and that this will increase device lifetimes but that efficiencies were reduced substantially due to interactions between the materials creating new low energy “charge transfer” states that are non-luminescent. Therefore, while our proposed strategy could in principle improve device lifetimes, we were unable to find a materials combination where the efficiency was not substantially compromised. In the course of our project, we made several important contributions that are peripherally related to the main project goal. First, we were able to prepare the proposed new family of materials and develop synthetic routes to make them efficiently. These types of materials that can transport both electrons and holes may yet have important roles to play in organic device technology. Second we developed an important new method for controlling the

  4. Characterization of aging in organic materials on atomic-, meso- and macro-length scales by {sup 13}C NMR spectroscopy

    SciTech Connect

    Assink, R.A.; Jamison, G.M.; Alam, T.M.; Gillen, K.T.

    1997-10-01

    A fundamental understanding of aging in an organic material requires that one understand how aging affects the chemical structure of a material, and how these chemical changes are related to the material`s macroscopic properties. This level of understanding is usually achieved by examining the material on a variety of length scales ranging from atomic to meso-scale to macroscopic. The authors are developing and applying several {sup 13}C nuclear magnetic resonance (NMR) spectroscopy experiments to characterize the aging process of organic materials over a broad range of length scales. Examples of studies which range from atomic to macroscopic will be presented.

  5. Extraction of organic materials from red water by metal-impregnated lignite activated carbon.

    PubMed

    Wei, Fangfang; Zhang, Yihe; Lv, Fengzhu; Chu, Paul K; Ye, Zhengfang

    2011-12-15

    Extraction of organic materials from 2,4,6-trinitrotoluene (TNT) red water by lignite activated carbon (LAC) impregnated with Cu(2+), Ba(2+), Sn(2+), Fe(3+), Ca(2+) and Ag(+) was investigated. The affinity to organic materials in red water was found to follow the order: Cu/LAC>Sn/LAC>Ag/LAC>Ba/LAC>Fe/LAC>Ca/LAC, which was explained by the hard and soft acid base (HSAB) theory. Cu(2+) showed the best performance and several parameters were further studied. X-ray photoelectron spectroscopy (XPS) verified effective loading of Cu(2+) on the LAC surface. The water quality before and after treated by Cu/LAC was evaluated using high performance liquid chromatograph, Gas Chromatography/Mass Spectroscopy (GC/MS), UV-vis spectroscopy and other analyses. The extraction performances and mechanism of organic materials on Cu/LAC were investigated through static methods. The experimental results showed that Cu/LAC possessed stronger extraction ability for the sulfonated nitrotoluenes than the non-sulfonated nitrotoluenes, the kinetic data fitted the pseudo-second-order kinetic model well. In addition, the leaching out of Cu(2+) from Cu/LAC was found much lower in the 100 times diluted red water (0.074%) than in the raw water (10.201%). Column adsorptions with more concentrated red water were also studied. Finally, Cu/LAC was observed to possess excellent reusability as well. PMID:22015039

  6. Electrochemical properties of new organic radical materials for lithium secondary batteries

    NASA Astrophysics Data System (ADS)

    Lee, Seo Hwan; Kim, Jae-Kwang; Cheruvally, Gouri; Choi, Jae-Won; Ahn, Jou-Hyeon; Chauhan, Ghanshyam S.; Song, Choong Eui

    The use of ionic liquid (IL)-supported organic radicals as cathode-active materials in lithium secondary batteries is reported in this article. Two different types of IL-supported organic radicals based on the 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) radical and imidazolium hexafluorophosphate IL were synthesized. The first type is a mono-radical with one unit of TEMPO and the second is a symmetrical di-radical with 2 U of TEMPO; both are viscous liquids at 25 °C. The radicals exhibit electrochemical activity at ∼3.5 V versus Li/Li + as revealed in the cyclic voltammetry tests. The organic radical batteries (ORBs) with these materials as the cathode, a lithium metal anode and 1 M LiPF 6 in EC/DMC electrolyte exhibited good performance at room temperature during the charge-discharge and cycling tests. The batteries exhibited specific capacities of 59 and 80 mAh g -1 at 1 C-rate with the mono- and di-radicals as the cathodes, respectively, resulting in 100% utilization of the materials. The performance degradation with increasing C-rate is very minimal for the ORBs, thus demonstrating good rate capability.

  7. Processing of meteoritic organic materials as a possible analog of early molecular evolution in planetary environments

    PubMed Central

    Pizzarello, Sandra; Davidowski, Stephen K.; Holland, Gregory P.; Williams, Lynda B.

    2013-01-01

    The composition of the Sutter’s Mill meteorite insoluble organic material was studied both in toto by solid-state NMR spectroscopy of the powders and by gas chromatography–mass spectrometry analyses of compounds released upon their hydrothermal treatment. Results were compared with those obtained for other meteorites of diverse classifications (Murray, GRA 95229, Murchison, Orgueil, and Tagish Lake) and found to be so far unique in regard to the molecular species released. These include, in addition to O-containing aromatic compounds, complex polyether- and ester-containing alkyl molecules of prebiotic appeal and never detected in meteorites before. The Sutter’s Mill fragments we analyzed had likely been altered by heat, and the hydrothermal conditions of the experiments realistically mimic early Earth settings, such as near volcanic activity or impact craters. On this basis, the data suggest a far larger availability of meteoritic organic materials for planetary environments than previously assumed and that molecular evolution on the early Earth could have benefited from accretion of carbonaceous meteorites both directly with soluble compounds and, for a more protracted time, through alteration, processing, and release from their insoluble organic materials. PMID:24019471

  8. Evaluation of surface damage on organic materials irradiated with Ar cluster ion beam

    SciTech Connect

    Yamamoto, Y.; Ichiki, K.; Ninomiya, S.; Matsuo, J.; Seki, T.; Aoki, T.

    2011-01-07

    The sputtering yields of organic materials under large cluster ion bombardment are much higher than those under conventional monomer ion bombardment. The sputtering rate of arginine remains constant with fluence for an Ar cluster ion beam, but decreases with fluence for Ar monomer. Additionally, because Ar cluster etching induces little damage, Ar cluster ion can be used to achieve molecular depth profiling of organic materials. In this study, we evaluated the damage to poly methyl methacrylate (PMMA) and arginine samples irradiated with Ar atomic and Ar cluster ion beams. Arginine samples were analyzed by secondary ion mass spectrometry (SIMS) and PMMA samples were analyzed by X-ray photoelectron spectroscopy (XPS). The chemical structure of organic materials remained unchanged after Ar cluster irradiation, but was seriously damaged. These results indicated that bombardment with Ar cluster ions induced less surface damage than bombardment with Ar atomic ion. The damage layer thickness with 5 keV Ar cluster ion bombardment was less than 1 nm.

  9. New organic-inorganic hybrid material based on functional cellulose nanowhisker, polypseudorotaxane and Au nanorods.

    PubMed

    Garavand, Ali; Dadkhah Tehrani, Abbas

    2016-11-01

    Organic-inorganic functional hybrid materials play a major role in the development of advanced functional materials and recently have gained growing interest of the worldwide community. In this context, new hybrid organic-inorganic gel consisting of cellulose nanowhisker xanthate (CNWX) and S-H functionalized polypseudorotaxane (PPR) as organic parts of gel and gold nanorods (GNRs) as inorganic cross-linking agent were prepared. Firstly, thiolated α-cyclodextrin (α-CD-SH) was threaded onto poly-(ethylene glycol) bis (mercaptoethanoate ester) (PEG-SH) to give polypseudorotaxane (PPR) and then it reacted with GNRs in the presence of CNWX to give the new hybrid gel material. The new synthesized gel and its components characterized by spectroscopic measurement methods such as FT-IR, UV-vis and NMR spectroscopy. Interestingly, hybrid gel showed new polygonal plate like morphology with 45-60nm thickness and 400-600nm width. The obtained gel may have potential application in many fields especially in biomedical applications. PMID:27516265

  10. The Role of Synthetic and Biologic Materials in the Treatment of Pelvic Organ Prolapse

    PubMed Central

    Brown, Ramon A.; Ellis, C. Neal

    2014-01-01

    Pelvic organ prolapse is a significant medical problem that poses a diagnostic and management dilemma. These diseases cause serious morbidity in those affected and treatment is sought for relief of pelvic pain, rectal bleeding, chronic constipation, obstructed defecation, and fecal incontinence. Numerous procedures have been proposed to treat these conditions; however, the search continues as colorectal surgeons attempt to find the procedure that would optimally treat these conditions. The use of prosthetics in the repair of pelvic organ prolapse has become prevalent as the benefits of their use are realized. While advances in biologic mesh and new surgical techniques promise improved functional outcomes with decreased complication rates without de novo symptoms, the debate concerning the best prosthetic material, synthetic or biologic, remains controversial. Furthermore, laparoscopic ventral mesh rectopexy has emerged as a procedure that could potentially fill this role and is rapidly becoming the procedure of choice for the surgical treatment of pelvic organ prolapse. PMID:25435827

  11. Reclaiming a natural beauty: whole-organ engineering with natural extracellular materials.

    PubMed

    Traphagen, Samantha; Yelick, Pamela C

    2009-09-01

    The ability to engineer whole organs as replacements for allografts and xenografts is an ongoing pursuit in regenerative medicine. While challenges remain, including systemic tissue integration with angiogenesis, lymphatiogenesis and neurogenesis, ongoing efforts are working to develop novel technologies to produce implantable engineered scaffolds and potentially engineered whole organs. Natural extracellular matrix materials, commonly utilized in vitro, are now being used as effective, natural, acellular allografts, and are being integrated into nanoscale scaffolds and matrices with programmable responsiveness. Based on the significant use of natural scaffolds for tissue regeneration and bioengineering strategies, this review focuses on recent and ongoing efforts to engineer whole organs, such as the tooth, featuring natural extracellular matrix molecules. PMID:19761399

  12. Quantitative EDXS analysis of organic materials using the ζ-factor method.

    PubMed

    Fladischer, Stefanie; Grogger, Werner

    2014-01-01

    In this study we successfully applied the ζ-factor method to perform quantitative X-ray analysis of organic thin films consisting of light elements. With its ability to intrinsically correct for X-ray absorption, this method significantly improved the quality of the quantification as well as the accuracy of the results compared to conventional techniques in particular regarding the quantification of light elements. We describe in detail the process of determining sensitivity factors (ζ-factors) using a single standard specimen and the involved parameter optimization for the estimation of ζ-factors for elements not contained in the standard. The ζ-factor method was then applied to perform quantitative analysis of organic semiconducting materials frequently used in organic electronics. Finally, the results were verified and discussed concerning validity and accuracy. PMID:24012932

  13. Different materials as a cathode modification layer on the impact of organic solar cells

    NASA Astrophysics Data System (ADS)

    Zhong, Jian; Huang, Qiuyan; Yu, Junsheng; Jiang, Yadong

    2010-10-01

    Organic thin film solar cells based on conjugated polymer or small molecules have showed an interesting approach to energy conversion since Tang reported a single donor-accepter hetero-junction solar cell. The power conversion efficiency of organic solar cells has increased steadily over last decade. Small-molecular weight organic double heterojunction donor-acceptor layer organic solar cells (OSC) with a structure of indium-tin-oxide (ITO)/CuPc(200Å)/C60(400Å)/x/Ag(1000Å), using CuPc(copper Phthalocyanine)as donor layer, and Alq3(8-Hydroxyquinoline aluminum salt), BCP(Bromocresol purple sodium salt) and Bphen(4'7-diphyenyl-1,10-phenanthroline) as cathode modification layer, respectively were fabricated. The performance of OSC was studied as a function of the different materials as an cathode modification layer to optimize the structure. The current-voltage characteristic of the solar cell under AM1.5 solar illumination at an intensity of 100 mw/cm2 showed that the power conversion efficiency (PCE) was dependent of the different materials of the cathode modification layer. the efficiency along with the different materials as an cathode modification layer will diminish under that standard solar illumination(AM1.5)was obtained. Using a double heterostructure of ITO/CuPc(200Å)/C60(400Å)/Alq3(60Å)/Ag(1000Å) with high-vacuum evaporation technology, the efficiency was 0.587%.the efficiency was 0.967% when the material of the cathode modification layer was BCP, with the structure of ITO/CuPc(200Å)/C60(400Å)/BCP(35Å)/Ag(1000Å), and the efficiency was 0.742% when the material of the cathode modification layer was Bphen, with the structure of ITO/CuPc(200Å)/C60(400Å)/ Bphen(50Å)/Ag(1000Å).Using different materials as a cathode modification layer, it can be seen that the material which matches the energy level could even eventually be able to improve the energy conversion efficiency more.

  14. Plant growth response in experimental soilless mixes prepared from coal combustion products and organic waste materials

    SciTech Connect

    Bardhan, S.; Watson, M.; Dick, W.A.

    2008-07-15

    Large quantities of organic materials such as animal manures, yard trimmings, and biosolids are produced each year. Beneficial use options for them are often limited, and composting has been proposed as a way to better manage these organic materials. Similarly, burning of coal created 125 million tons of coal combustion products (CCP) in the United States in 2006. An estimated 53 million tons of CCP were reused, whereas the remainder was deposited in landfills. By combining CCP and composted organic materials (COM), we were able to create soilless plant growth mixes with physicochemical conditions that can support excellent plant growth. An additional benefit is the conservation of natural raw materials, such as peat, which is generally used for making soilless mixes. Experimental mixes were formulated by combining CCP and COM at ratios ranging from 2:8 to 8:2 (vol/vol), respectively. Water content at saturation for the created mixes was 63% to 72%, whereas for the commercial control, it was 77%. pH values for the best performing mixes ranged between 5.9 and 6.8. Electrical conductivity and concentrations of required plant nutrient were also within plant growth recommendations for container media. Significantly (P < 0.0001) higher plant biomass growth (7%-130%) was observed in the experimental mixes compared with a commercial mix. No additional fertilizers were provided during the experiment, and reduced fertilization costs can thus accrue as an added benefit to the grower. In summary, combining CCP and COM, derived from source materials often viewed as wastes, can create highly productive plant growth mixes.

  15. Search for greener Li-ion batteries: an alternative offered by organic electroactive materials

    NASA Astrophysics Data System (ADS)

    Geng, Joaquin; Renault, Stéven; Poizot, Philippe; Dolhem, Franck

    2011-06-01

    The threats of climate change and the issues of secure energy supply are among the fundamental challenges of the 21stcentury that push humanity to adopt a sustainable development and to favour the use of renewable sources of energy. In addition to their historical use, LIBs seem on the road to power the next "Zero Emission" vehicles or could be used to assist the integration of renewable energy sources both on- and off-the-grid. Consequently, production of LIBs is expected to keep on growing. However LIBs are nearly exclusively based on inorganic compounds, non-renewable and energy-greedy materials. Thus in parallel with regular research on inorganic-based LIBs, we have recently proposed to probe an alternative pathway by searching for redox-active organic materials, easier to discard while possibly derived from biomass resources. As solid-state electrochemistry of organics is not that well documented, our current approach consists in a global survey of selected organic structures in order to grasp relevant parameters that affect the redox potential, the stability upon cycling and so on. In this report, we extend our current database of redox-active organic structures by evaluating vs. Li bulky pyrazine-based structures and dilithium polyporate as a supplementary specimen of p-benzoquinone derivatives.

  16. Abundance of Cosmogenic Noble Gases as a Marker of the Organic Degradation by Cosmic Rays in the Surface Martian Rocks. Implications to MSL and Mars 2020

    NASA Astrophysics Data System (ADS)

    Pavlov, A. A.; Vasilyev, G. I.; Ostryakov, V. M.; Pavlov, A. K.; Mahaffy, P.

    2014-07-01

    We conducted a modeling study which links the rates of cosmogenic isotopes production with the radiation accumulation rates on Mars. We calculated the degradation level of the organic molecules at Cumberland based on the observed cosmogenic isotopes.

  17. Carbon dioxide emissions from agricultural soils amended with livestock-derived organic materials

    NASA Astrophysics Data System (ADS)

    Pezzolla, D.; Said-Pullicino, D.; Gigliotti, G.

    2009-04-01

    Carbon dioxide gas xchange between terrestrial ecosystems and the atmosphere, as well as the carbon sink strength of various arable land ecosystems, is of primary interest for global change research. Measures for increasing soil C inputs include the preferential use of livestock-derived organic materials (e.g. animal manure and slurries, digestate from biogas production plants and compost). The application of such materials to agricultural soils returns essential nutrients for plant growth and organic matter to maintain long-term fertility. Whether or not such practices ultimately result in sustained C sequestration at the ecosystem level will depend on their mineralization rates. This work presents preliminary results from a laboratory incubation trial to evaluate carbon dioxide fluxes from two agricultural soils (a calcareous silt loam and a silty clay loam) amended with agricultural doses of (i) pig slurry (PSL), (ii) the digestate from the anaerobic fermentation of pig slurries (AAS) and (ii) a compost from the aerobic stabilisation of the digestate (LDC). These subsequent steps of slurry stabilisation resulted in a decrease in the content of labile organic matter which was reflected in a reduction in maximum carbon dioxide emission rates from amended soils. Measurements have shown that peak emissions from soils occur immediately after application of these organic materials (within 5 days) and decrease in the order PSL > AAS > LDC. Moreover, mean cumulative emissions over the first 40 days showed that a higher percentage (about 44%) of the C added with PSL was mineralised respect to C added with AAS (39%) and LDC (25%). Although it was hypothesised that apart from the quantity and stability of the added organic materials, even soil characteristics could influence C mineralisation rates, no significant differences were observed between emission fluxes for similarly treated soils. Mean cumulative emission fluxes after 40 days from treatment were of 114, 103 and

  18. Hydroxyl-decorated Graphene Systems: Organic metal-free Ferroelectrics, Multiferroics, and Proton battery Cathode Materials

    NASA Astrophysics Data System (ADS)

    Wu, Menghao; Burton, J. D.; Tsymbal, Evgeny; Zeng, Xiao; Jena, Puru; Jena's Group Team, Prof.; Burton's Group Team, Prof.; Tsymbal's Group Team, Prof.; Zeng's Group Team, Prof.

    2013-03-01

    Through density-functional-theory calculations we show that hydroxylized graphene systems are ideal candidates for light-weight organic ferroelectric materials with giant polarizations. For example, the polarization of semi-hydroxylized graphane and graphone as well as fully hydroxylized graphane are, respectively, 41.1, 43.7, 67.7 μC/cm2, much higher than any organic ferroelectric materials known to date. In addition, hydroxylized graphone is multiferroic due to the coexistence of ferroeletricity and ferromagnetism. Zigzag graphene nanoribbons decorated by hydroxyl groups also exhibit ferroelectric properties with a large polarization of 27.0 μC/cm2. Moreover, proton vacancies at the end of ribbons can induce large dipole moments that can be reversed by both hopping of protons and rotation of O-H bonds under an electric field. These materials have the potential as high-capacity cathode materials with specific capacity six times larger than lead-acid batteries and five times that of lithium-ion batteries.

  19. Anisotropic hybrid organic/inorganic (azopolymer/SiO2 NP) materials with enhanced photoinduced birefringence.

    PubMed

    Nazarova, Dimana; Nedelchev, Lian; Sharlandjiev, Peter; Dragostinova, Violeta

    2013-08-01

    Hybrid materials based on combination of polymers and inorganic nanoparticles (NP) attracted considerable attention in the last decade due to their advantageous electrical, optical, or mechanical properties. Recently, we reported a significant improvement of the photoresponse by doping azopolymers with ZnO NP. To study the influence of the composition of the dopant, in our present work we have synthesized anisotropic organic/inorganic nanocomposite materials by incorporating 5-15 nm sized SiO2 NP in a side-chain azopolymer. As a result we observe an enhancement of the photoinduced birefringence in these composite materials with about 20% compared to the nondoped sample. Additionally, we discuss possible mechanisms leading to this enhancement related with the scattering caused by the NP and the increased mobility of the azochromophores in the vicinity of NP. PMID:23913084

  20. Synthesis of Inorganic-Organic Hybrid Materials Designed for Radiation Detection, Luminescence, and Gas Storage

    NASA Astrophysics Data System (ADS)

    Vaughn, Shae Anne

    Materials discovery is the driving force behind the research presented herein. Basic research has been conducted in order to obtain a better understanding of coordination chemistry and structural outcomes, particularly within the area of trivalent lanthanides. Discovering new materials is one route to further advancement of technology; another one is the focus on incremental changes to already existing materials. Often the building blocks of a compound are chosen in an effort to synthesize a material that makes use of the properties of each individual component and may result in a better, more robust, applicable material. The combination of organic and inorganic components for the synthesis of novel materials with potential applications such as scintillation photoluminescence, catalysis, and gas storage are the focus of the research presented herein. The first part focuses on lanthanide organic hybrid materials, where the synthesis of a new family of potential scintillating materials was undertaken and yielded improved understanding of the control that can be achieved over the topological structure of these materials by controlling the coordinating crystallization solvents. This research has led to the synthesis of an array of unique motifs, ranging from dimeric complexes, tetrameric complexes, to 1-D chains, and most intriguing of all, catenated tetradecanuclear rings. These rings represent the largest lanthanide rings synthesized to date, the next largest multinuclear rings, until now, were dodecanuclear complexes of alkoxides. From a basic research standpoint this is an exciting new development in lanthanide coordination chemistry and illustrates the importance of steric effects upon a system. These complexes are potential scintillators, supported by their luminescence and measurements of similar compounds that demonstrate surprising scintillation efficiencies. In the second part, other hybrid materials that have also been prepared are discussed, including the