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Sample records for 4-styrene sulfonate pss

  1. Electromechanical properties of poly(3,4-ethylenedioxythiophene)/poly(4-styrene sulfonate) films.

    PubMed

    Okuzaki, Hidenori; Suzuki, Hiroki; Ito, Takamichi

    2009-08-20

    Free-standing films made of poly(3,4-ethylenedioxythiophene) doped with poly(4-styrene sulfonate) (PEDOT/PSS) were prepared by casting water dispersion of its colloidal particles. Morphology, water vapor sorption, and electro-active polymer actuating behavior of the resulting films were investigated by means of atomic force microscopy, sorption isotherm, thermal mechanical analysis, and electromechanical analysis. It was found that the PEDOT/PSS film sorbed 60% of moisture at relative water vapor pressure of 0.95. Upon application of 10 V, the film underwent contraction of 2.4% in air at 50% relative humidity (RH) which significantly increased to 4.5% at 90% RH. The principle lay in desorption of water vapor sorbed in the film due to Joule heating, where electric field was capable of controlling the equilibrium of water vapor sorption. The film generated contractile stress as high as 17 MPa under isometric conditions and work capacity attained 174 kJ m(-3), where Young's modulus of the film increased from 1.8 to 2.6 GPa by application of 6 V at 50% RH.

  2. Nanostructured bacterial cellulose-poly(4-styrene sulfonic acid) composite membranes with high storage modulus and protonic conductivity.

    PubMed

    Gadim, Tiago D O; Figueiredo, Andrea G P R; Rosero-Navarro, Nataly C; Vilela, Carla; Gamelas, José A F; Barros-Timmons, Ana; Neto, Carlos Pascoal; Silvestre, Armando J D; Freire, Carmen S R; Figueiredo, Filipe M L

    2014-05-28

    The present study reports the development of a new generation of bio-based nanocomposite proton exchange membranes based on bacterial cellulose (BC) and poly(4-styrene sulfonic acid) (PSSA), produced by in situ free radical polymerization of sodium 4-styrenesulfonate using poly(ethylene glycol) diacrylate (PEGDA) as cross-linker, followed by conversion of the ensuing polymer into the acidic form. The BC nanofibrilar network endows the composite membranes with excellent mechanical properties at least up to 140 °C, a temperature where either pure PSSA or Nafion are soft, as shown by dynamic mechanical analysis. The large concentration of sulfonic acid groups in PSSA is responsible for the high ionic exchange capacity of the composite membranes, reaching 2.25 mmol g(-1) for a composite with 83 wt % PSSA/PEGDA. The through-plane protonic conductivity of the best membrane is in excess of 0.1 S cm(-1) at 94 °C and 98% relative humidity (RH), decreasing to 0.042 S cm(-1) at 60% RH. These values are comparable or even higher than those of ionomers such as Nafion or polyelectrolytes such as PSSA. This combination of electric and viscoelastic properties with low cost underlines the potential of these nanocomposites as a bio-based alternative to other polymer membranes for application in fuel cells, redox flow batteries, or other devices requiring functional proton conducting elements, such as sensors and actuators.

  3. Synthesis of Ru(0.58)In(0.42)O(y)⋅nH(2)O nanoparticles dispersed onto poly(sodium-4-styrene sulfonate)-functionalized multi-walled carbon nanotubes and their application for electrochemical capacitors.

    PubMed

    Yuan, Changzhou; Hou, Linrui; Yang, Long; Li, Diankai; Tan, Jie; Shen, Laifa; Zhang, Fang; Zhang, Xiaogang

    2011-02-15

    In this work, poly(sodium-4-styrene sulfonate) (PSS)-functionalized multi-walled carbon nanotubes (FMWCNTs) were first synthesized via a polymer-assisted technique. Then, Ru(0.58)In(0.42)O(y)⋅nH(2)O nanoparticles (NPs) were mono-dispersed onto the FMWCNTs surfaces under mild hydrothermal condition. Here, PSS with negative charge serves as a bifunctional molecule both for solubilizing and dispersing MWCNTs into aqueous solution and for tethering Ru(3+) and In(3+) to facilitate the good dispersion of Ru(1-)(x)In(x)O(y)⋅nH(2)O NPs onto their surfaces. The good dispersion of Ru(0.58)In(0.42)O(y)⋅nH(2)O NPs onto FMWCNTs makes OH(-) ions and electrons easily contact these NPs with abundant electroactive sites, which results in a large specific capacitance (SC) of 319Fg(-1) for the naocomposites. Moreover, a symmetric electrochemical capacitor (EC) is constructed by using the nanocomposites as electrodes and delivers large specific energy density of 18.1Whkg(-1), desirable power property of 1302Wkg(-1), high electrochemical reversibility and good SC retention of 84.7%.

  4. Direct laser interference patterning of poly(3,4-ethylene dioxythiophene)-poly(styrene sulfonate) (PEDOT-PSS) thin films

    NASA Astrophysics Data System (ADS)

    Lasagni, Andrés F.; Hendricks, Jeffrey L.; Shaw, Charles M.; Yuan, Dajun; Martin, David C.; Das, Suman

    2009-08-01

    We have developed a patterning procedure based on selective ablation using interference patterns with ns-laser pulses to fabricate periodic arrays on large areas of poly(3,4-ethylene dioxythiophene)-poly(4-styrene sulfonic acid) (PEDOT-PSS) thin films over a metallic gold-palladium layer. Single pulse laser-ablation experiments were performed to study the ablation characteristics of the thin films as a function of the film thickness. The ablation threshold fluence of the PEDOT-PSS films was found to be dependent on thickness with values ranging from 43 mJ/cm 2 to 252 mJ/cm 2. Additionally, fluences at which the PEDOT-PSS films could be ablated without inducing damage in the underlying metallic films were observed (128 mJ/cm 2 and 402 mJ/cm 2 for film thicknesses of 70 nm and 825 nm, respectively). Linear periodic arrays with line spacings of 7.82 μm and 13.50 μm were also fabricated. The surface topography of these arrays was analyzed using scanning electron and atomic force microscopy. For thicker polymeric layers, several peeled sub-layers of the conjugated polymer with average thicknesses of about 165-185 nm were observed in the ablation experiments. The size and scale of structures produced by this technique could be suitable for several biomedical applications and devices in which controlling cell adhesion, promoting cell alignment, or improving biocompatibility are important.

  5. Preparation of graphene oxide/poly (3,4-ethylenedioxytriophene): Poly (styrene sulfonate) (PEDOT:PSS) electrospun nanofibers

    NASA Astrophysics Data System (ADS)

    Efelina, Vita; Widianto, Eri; Rusdiana, Dadi; Nugroho, A. A.; Kusumaatmaja, Ahmad; Triyana, Kuwat; Santoso, Iman

    2016-04-01

    Graphene oxide (GO)/Poly (3,4-Ethylenedioxytriophene):Poly (styrene Sulfonate) (PEDOT:PSS) nanofibers have been successfully fabricated by a simple electrospinning technique to develop conductive nanofibers with polyvinyl alcohol (PVA) act as a carrier solution. Graphene oxide has been synthesized by Hummer's method and has been confirmed by Raman Spectroscopy, FTIR and UV-Vis Spectroscopy. GO/PEDOT:PSS composite nanofibers. The structural and morphological properties were characterized by Scanning Electron Microscopy (SEM). The result of SEM show that GO/PEDOT:PSS nanofibers has a relatively uniform morphology nanofiber with diameter between 180 nm - 340 nm with smooth nanofiber surface. The produced nanofibers from this study can be utilized for various applications such as flexible, conductive and transparent electrode.

  6. Preparation of graphene oxide/poly (3,4-ethylenedioxytriophene): Poly (styrene sulfonate) (PEDOT:PSS) electrospun nanofibers

    NASA Astrophysics Data System (ADS)

    Widianto, Eri; Efelina, Vita; Rusdiana, Dadi; Nugroho, A. A.; Kusumaatmaja, Ahmad; Triyana, Kuwat; Santoso, Iman

    2016-04-01

    Graphene oxide (GO)/Poly (3,4-Ethylenedioxytriophene):Poly (styrene Sulfonate) (PEDOT:PSS)nanofibers have been successfully fabricated by a simple electrospinning technique to develop conductive nanofibers with polyvinyl alcohol (PVA) act as a carrier solution. Graphene oxide hasbeen synthesized by Hummer's method and has been confirmed by Raman Spectroscopy, FTIR, and UV-Vis Spectroscopy. The structural and morphological properties of GO/PEDOT:PSS composite nanofiberswere characterized by Scanning Electron Microscopy (SEM). The result of SEM showed that GO/PEDOT:PSS nanofibers have a relatively uniform morphology nanofiber with adiameterof 180 nm - 340 nm with smooth nanofiber surface. The produced nanofibers from this study can be utilized for various applicationssuch as aflexible, conductive and transparent electrode.

  7. Development of bifacial inverted polymer solar cells using a conductivity-controlled transparent PEDOT:PSS and a striped Au electrode on the hole collection side

    NASA Astrophysics Data System (ADS)

    Kuwabara, Takayuki; Katori, Shinji; Arima, Kazuhiro; Omura, Yoshihiro; Yamaguchi, Takahiro; Taima, Tetsuya; Takahashi, Kohshin

    2014-02-01

    An inverted bifacial polymer solar cell was developed using a conductivity-controlled transparent poly(3,4-ethylenedioxylenethiophene):poly(4-styrene sulfonic acid) (PEDOT:PSS) as a hole collection layer and a striped Au electrode with a large open aperture ratio (Rap) as a hole collection electrode. We investigated the performance of the device by varying the interelectrode distance of the striped Au electrode and the sheet resistance of the PEDOT:PSS film. The device using untreated Clevios P (PEDOT:PSS) showed a maximum electric output (Pw) in the Rap range of 50 to 65%. When alcohol-treated Clevios P (Clevios P+) with a lower electrical resistance was used, the maximum Pw increased by 40% compared with that of the device using Clevios P. The maximum Pw was obtained in the Rap range of 84% as the hole collection efficiency of the striped Au electrode improved with the decreased sheet resistance of the PEDOT:PSS.

  8. New 2-in-1 polyelectrolyte step-by-step film buildup without solution alternation: from PEDOT-PSS to polyelectrolyte complexes.

    PubMed

    de Saint-Aubin, Christine; Hemmerlé, Joseph; Boulmedais, Fouzia; Vallat, Marie-France; Nardin, Michel; Schaaf, Pierre

    2012-06-12

    Although never emphasized and increasingly used in organic electronics, PEDOT-PSS (poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate)) layer-by-layer (lbl) film construction violates the alternation of polyanion and polycation rule stated as a prerequisit for a step-by-step film buildup. To demonstrate that this alternation is not always necessary, we studied the step-by-step construction of films using a single solution containing polycation/polyanion complexes. We investigated four different systems: PEDOT-PSS, bPEI-PSS (branched poly(ethylene imine)-poly(sodium 4-styrene sulfonate)), PDADMA-PSS (poly(diallyl dimethyl ammonium)-PSS), and PAH-PSS (poly(allylamine hydrochloride)-PSS). The film buildup obtained by spin-coating or dipping-and-drying process was monitored by ellipsometry, UV-vis-NIR spectrophotometry, and quartz-crystal microbalance. The surface morphology of the films was characterized by atomic force microscopy in tapping mode. After an initial transient regime, the different films have a linear buildup with the number of deposition steps. It appears that, when the particles composed of polyanion-polycation complex and complex aggregates in solution are more or less liquid (case of PEDOT-PSS and bPEI-PSS), our method leads to smooth films (roughness on the order of 1-2 nm). On the other hand, when these complexes are more or less solid particles (case of PDADMA-PSS and PAH-PSS), the resulting films are much rougher (typically 10 nm). Polycation/polyanion molar ratios in monomer unit of the liquid, rinsing, and drying steps are key parameters governing the film buildup process with an optimal polycation/polyanion molar ratio leading to the fastest film growth. This new and general lbl method, designated as 2-in-1 method, allows obtaining regular and controlled film buildup with a single liquid containing polyelectrolyte complexes and opens a new route for surface functionalization with polyelectrolytes.

  9. Dependence of Device Characteristics of Bulk-Heterojunction Organic Thin-Film Solar Cells on Concentration of Glycerol and Sorbitol Addition in Pedot:. PSS Solutions for Fabricating Buffer Layers

    NASA Astrophysics Data System (ADS)

    Yamaki, Yusuke; Marumoto, Kazuhiro; Fujimori, Takuya; Mori, Tatsuo

    We have investigated the dependence of device characteristics of bulk-heterojunction organic thin-film solar cells on the concentration of glycerol and sorbitol addition in poly(3,4-ethylenedioxy thiophene):poly(4-styrene sulfonate) (PEDOT:PSS) solutions for fabricating buffer layers. The device structure is ITO/buffer/regioregular poly(3-hexylthiophene) (P3HT):[6,6]-phenyl C61-butyric acid methylester (PCBM)/Al. Glycerol addition is effective for increasing power conversion efficiency (PCE) from 1.25 to 1.41% because of the increase in short-circuit current density (Jsc) without decreasing open-circuit voltage (Voc). On the other hand, sorbitol addition decreases PCE from 1.25 to 1.04%, owing to the decrease in Voc. This difference in Voc behavior is ascribed to different work function of PEDOT:PSS with glycerol and sorbitol treatment.

  10. Composite films of oxidized multiwall carbon nanotube and poly(3,4-ethylenedioxythiophene): polystyrene sulfonate (PEDOT:PSS) as a contact electrode for transistor and inverter devices.

    PubMed

    Yun, Dong-Jin; Rhee, Shi-Woo

    2012-02-01

    Composite films of multiwall carbon nanotube (MWNT)/poly(3,4-ethylenedioxythiophene) polymerized with poly(4-styrenesulfonate) (PEDOT:PSS) were prepared by spin-coating a mixture solution. The effect of the MWNT loading and the MWNT oxidation, with acid solution or ultraviolet (UV)-ozone treatment, on the film properties such as surface roughness, work function, surface energy, optical transparency and conductivity were studied. Also pentacene thin film transistors and inverters were made with these composite films as a contact metal and the device characteristics were measured. The oxidation of MWNT reduced the conductivity of MWNT/PEDOT:PSS composite film but increased the work function and transparency. UV-ozone treated MWNT/PEDOT:PSS composite film showed higher conductivity (14000 Ω/□) and work function (4.9 eV) than acid-oxidized MWNT/PEDOT:PSS composite film and showed better performance as a source/drain electrode in organic thin film transistor (OTFT) than other types of MWNT/PEDOT:PSS composite films. Hole injection barrier of the UV-ozone treated MWNT/PEDOT:PSS composite film with pentacene was significantly lower than any other films because of the higher work function. PMID:22264140

  11. Phase Behavior of Symmetric Sulfonated Block Copolymers

    SciTech Connect

    Park, Moon Jeong; Balsara, Nitash P.

    2008-08-21

    Phase behavior of poly(styrenesulfonate-methylbutylene) (PSS-PMB) block copolymers was studied by varying molecular weight, sulfonation level, and temperature. Molecular weights of the copolymers range from 2.9 to 117 kg/mol. Ordered lamellar, gyroid, hexagonally perforated lamellae, and hexagonally packed cylinder phases were observed in spite of the fact that the copolymers are nearly symmetric with PSS volume fractions between 0.45 and 0.50. The wide variety of morphologies seen in our copolymers is inconsistent with current theories on block copolymer phase behavior such as self-consistent field theory. Low molecular weight PSS-PMB copolymers (<6.2 kg/mol) show order-order and order-disorder phase transitions as a function of temperature. In contrast, the phase behavior of high molecular weight PSS-PMB copolymers (>7.7 kg/mol) is independent of temperature. Due to the large value of Flory-Huggins interaction parameter, x, between the sulfonated and non-sulfonated blocks, PSS-PMB copolymers with PSS and PMB molecular weights of 1.8 and 1.4 kg/mol, respectively, show the presence of an ordered gyroid phase with a 2.5 nm diameter PSS network. A variety of methods are used to estimate x between PSS and PMB chains as a function of sulfonation level. Some aspects of the observed phase behavior of PSS-PMB copolymers can be rationalized using x.

  12. Electrostatic Effect on the Solution Structure and Dynamics of PEDOT:PSS

    NASA Astrophysics Data System (ADS)

    Leaf, Michael; Muthukumar, Murugappan

    Poly(3,4-ethylenedioxythiophene):poly(styrene sulfonic acid) (PEDOT:PSS) is a popular material used in organic electronic devices as a conductor. It consists of PEDOT polycations complexed with PSS polyanions which are initially suspended in aqueous solution and eventually cast into a film. Various annealing and doping methods dramatically enhance PEDOT:PSS film conductivity. To understand the physical interactions at play, we explore structural and dynamic aspects of PEDOT:PSS solutions through scattering and rheology techniques. We highlight several aspects of the phase behavior of PEDOT:PSS, and the significance of electrostatic interactions.

  13. Ultraviolet-ozone-treated PEDOT:PSS as anode buffer layer for organic solar cells.

    PubMed

    Su, Zisheng; Wang, Lidan; Li, Yantao; Zhao, Haifeng; Chu, Bei; Li, Wenlian

    2012-08-17

    Ultraviolet-ozone-treated poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS)was used as the anode buffer layer in copper phthalocyanine (CuPc)/fullerene-based solar cells. The power conversion efficiency of the cells with appropriated UV-ozone treatment was found to increase about 20% compared to the reference cell. The improved performance is attributed to the increased work function of the PEDOT:PSS layer, which improves the contact condition between PEDOT:PSS and CuPc, hence increasing the extraction efficiency of the photogenerated holes and decreasing the recombination probability of holes and electrons in the active organic layers.

  14. Coarse graining of polystyrene sulfonate

    NASA Astrophysics Data System (ADS)

    Perahia, Dvora; Agrawal, Anupriya; Grest, Gary S.

    2015-03-01

    Capturing large length scales in soft matter while retaining atomistic properties is imperative to computational studies. Here we develop a new coarse-grained model for polystyrene sulfonate (PSS) that often serves as a model system because of its narrow molecular weight distribution and defined degree of sulfonation. Four beads are used to represent polymer where the backbone, the phenyl group, and the sulfonated group are each represented by a different bead and the fourth one represents counterion, which is sodium in our case. Initial atomistic simulations of PSS melt with sulfonation levels of 2-10%, with a dielectric constant ɛ = 1 revealed a ``locked'' phase where motion of the polymer is limited. Dielectric constant of ɛ = 5 was used to accelerate the dynamics. Bonded interactions were obtained using Boltzmann inversion on the bonded distributions extracted from atomistic simulation. Non-bonded interaction of polystyrene monomer was taken from our previous work and potential of mean force was used as the initial guess for interaction of the ionic beads. This set of potential was subsequently iterated to get a good match with radial distribution functions. This potential and its transferability across dielectric constants and temperatures will be presented. Grant DE-SC007908.

  15. Solvation Behavior of Short-chain Polystyrene Sulfonate in Aqueous Electrolyte Solutions: A Molecular Dyamics Study

    SciTech Connect

    Chialvo, Ariel A; Simonson, J Michael {Mike}

    2005-01-01

    We analyze the solvation behavior of short-chain polystyrene sulfonate (PSS) in aqueous electrolyte solutions by isothernal-isochoric molecular dynamics simulation to determine the solvation effects on the structure and conformation of the polyelectrolyte as a function of the aqueous environment. To that end, we study these aqueous systems including the explicit atomistic description of water, the PSS chain, and their interactions with all species in solution. In addition, we investigate the effect of the degree of sulfonation and its distribution along the PSS chain on the resulting conformation as well as solvation structure. Moreover, we assess the impact of added salts on the net charge of the PSS backbone, placing emphasis on the valence of the counterion and the extent of the ion-pair formation between the sulfonate group and the counterions. Finally, we present evidence for the so-called like-charge attraction between sulfonate groups through the formation of counterion-mediated interchain sulfonate-sulfonate and water-mediated intrachain sulfonate-sulfonate bridges, as well as between unlike counterion-counterion interactions.

  16. Aldicarb sulfone

    Integrated Risk Information System (IRIS)

    Aldicarb sulfone ; CASRN 1646 - 88 - 4 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic

  17. PUA/PSS multilayer coated CaCO3 microparticles as smart drug delivery vehicles.

    PubMed

    Du, Chao; Shi, Jun; Shi, Jin; Zhang, Li; Cao, Shaokui

    2013-10-01

    Hybrid CaCO3 microparticles coated by sodium poly(styrene sulfonate) (PSS) and aliphatic poly(urethane-amine) (PUA) were developed as thermal-/pH-responsive drug delivery vehicles via LbL self-assembly technique. The DOX release from the CaCO3 microparticles was higher than 60% within 36 h, whereas the value of PUA/PSS-coated microparticles was only 20%. The results demonstrated that the PUA/PSS multilayer coating could reduce the drug release rate and significantly assuage the initial burst release of DOX. In addition, the drug release of the hybrid microparticles was found to be thermal-/pH-dual responsive. More interestingly, more than 90% of DOX was released in 36 h at pH2.1 and 55 °C owing to the combined action of the dissolution of the CaCO3 core and the shrinkage of aliphatic PUA. PMID:23910272

  18. Increased work function in PEDOT:PSS film under ultraviolet irradiation

    NASA Astrophysics Data System (ADS)

    Xing, Ying-Jie; Qian, Min-Fang; Guo, Deng-Zhu; Zhang, Geng-Min

    2014-03-01

    An increase of work function (0.3 eV) is achieved by irradiating poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) film in vacuum with 254-nm ultraviolet (UV) light. The mechanism for such an improvement is investigated by photoelectron yield spectroscopy, X-ray photo electron energy spectrum, and field emission technique. Surface oxidation and composition change are found as the reasons for work function increase. The UV-treated PEDOT:PSS film is used as the hole injection layer in a hole-only device. Hole injection is improved by UV-treated PEDOT:PSS film without baring the enlargement of film resistance. Our result demonstrates that UV treatment is more suitable for modifying the injection barrier than UV ozone exposure.

  19. PUA/PSS multilayer coated CaCO3 microparticles as smart drug delivery vehicles.

    PubMed

    Du, Chao; Shi, Jun; Shi, Jin; Zhang, Li; Cao, Shaokui

    2013-10-01

    Hybrid CaCO3 microparticles coated by sodium poly(styrene sulfonate) (PSS) and aliphatic poly(urethane-amine) (PUA) were developed as thermal-/pH-responsive drug delivery vehicles via LbL self-assembly technique. The DOX release from the CaCO3 microparticles was higher than 60% within 36 h, whereas the value of PUA/PSS-coated microparticles was only 20%. The results demonstrated that the PUA/PSS multilayer coating could reduce the drug release rate and significantly assuage the initial burst release of DOX. In addition, the drug release of the hybrid microparticles was found to be thermal-/pH-dual responsive. More interestingly, more than 90% of DOX was released in 36 h at pH2.1 and 55 °C owing to the combined action of the dissolution of the CaCO3 core and the shrinkage of aliphatic PUA.

  20. Investigation of the doping efficiency of poly(styrene sulfonic acid) in poly(3,4-ethylenedioxythiophene)/poly(styrene sulfonic acid) dispersions by capillary electrophoresis.

    PubMed

    Diah, Anang W M; Quirino, Joselito P; Belcher, Warwick; Holdsworth, Clovia I

    2014-07-01

    CE can efficiently separate poly(3,4-ethylenedioxythiophene)/poly(styrene sulfonic acid) (PEDOT/PSS) complexes and free PSS in dispersions and can be used to estimate the degree of PSS doping. We investigated the doping efficiency of PSS on PEDOT in dispersions using CE and its effect on the conductivity of the resulting PEDOT/PSS films. Results of this study indicate that dispersions containing 1:2.5-3 EDOT:PSS feed ratio (by weight) exhibiting 72-73% PSS doping generate highly processable and highly conductive films. Conductivity can be optimized by limiting the time of reaction to 12 h. At this point of the reaction, the PEDOT/PSS segments, appearing as broad band in the electropherogram, could still exist in an extended coil conformation favoring charge transport resulting in high conductivity. Above a threshold PEDOT length formed at reaction times longer than 12 h, the PEDOT/PSS complex, appearing as spikes in the electropherogram, most likely have undergone a conformational change to coiled core-shell structure restricting charge transport resulting in low conductivity. The optimal conductivity (5.2 S/cm) of films from dispersions synthesized for 12 h is significantly higher than those from its commercial equivalent Clevios P and other reported values obtained under similar conditions without the addition of codopants. PMID:24782292

  1. Au Nanocluster assisted PCE improvement in PEDOT: PSS - Si Hybrid Devices

    NASA Astrophysics Data System (ADS)

    Sharma, Manisha; Pudasaini, Pushpa Raj; Ayon, Arturo A.

    2015-03-01

    Poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS), a P-type organic polymer is frequently employed in the fabrication of heterojunction p-n solar cell devices due to its proper HOMO-LUMO band gap as well as its tunable conductivity. In this report we describe the incorporation of gold (Au) nanoclusters in the PEDOT:PSS blend and its influence on the power-conversion-efficiency (PCE) on planar silicon (Si) hybrid heterojunction solar cell devices. Specifically, the reference samples without the aforementioned nanoclusters, were measured to exhibit a 6.10% PCE, value that increased to 7.55% upon the addition of the Au nanoclusters. The observed increase in the PCE is attributed to the enhanced electrical conductivity of the PEDOT:PSS films due to the incorporation of the nanoclusters, which is directly reflected in their improved fill factor. It is further theorized that the presence of Au nanoclusters in the insulating PSS layer in the PEDOT:PSS blend have a positive influence in the charge collection effectiveness of the devices produced. Considering that the Au nanoparticles involved in this research exercise had an average size of only 4 nm, it is considered that plasmonic effects did not play a relevant role in the observed PCE improvement.

  2. Improving the electrical conductivity of PEDOT:PSS films by binary secondary doping

    NASA Astrophysics Data System (ADS)

    Zhu, Zhengyou; Liu, Congcong; Xu, Jingkun; Jiang, Qinglin; Shi, Hui; Liu, Endou

    2016-01-01

    In this work, the electrical conductivity of poly(3,4-ethylenedioxythiophene): poly(styrene sulfonate) (PEDOT:PSS) films was effectively enhanced by binary secondary doping. Initially, doping with 5 vol.% dimethyl sulfoxide (DMSO) improved the electrical conductivity from 0.3 S cm-1 to 437 S cm-1 and a further increase to 950 S cm-1 was achieved by adding LiClO4. The conductivity value we report here is one of the highest reported for pretreated PEDOT:PSS films. The obtained maximum electrical conductivity is almost 3000 times higher than that shown by pristine PEDOT:PSS films. The increase in the electrical conductivity is ascribed to the synergistic effect of the two dopants. Fourier transform infrared spectra indicated the absence of any changes to the chemical structure of PEDOT:PSS. Atomic force microscopy images demonstrate an increased surface roughness and suggest the occurrence of conformational changes of PEDOT chains from the coiled to coil-extended one, which is the key reason for the electrical conductivity enhancement. The pretreatments we propose here are rapid, simple and effective for the large-scale preparation of high-conductivity PEDOT:PSS films. [Figure not available: see fulltext.

  3. Effect of glycerol on retention time and electrical properties of polymer bistable memory devices based on glycerol-modified PEDOT:PSS.

    PubMed

    Park, Boongik; Lee, Junhwan; Kim, Ohyun

    2012-01-01

    The addition of glycerol to Poly(3,4-ethylenedioxythiophene):Poly(styrene sulfonate) (PEDOT:PSS) films affected the bipolar switching characteristics of nonvolatile polymer memory devices (PMDs). Increasing the glycerol/PEDOT:PSS ratio caused increase in the OFF-current of the PMDs, but did not affect the ON-current levels. This result demonstrates that highly-conductive current paths occur in the ON-state. The write-read-erase-read cycle test was operated > 10(5) times. And, the ON-retention time is largely dependent on the glycerol to PEDOT:PSS ratio and annealing temperature. In addition, AFM analysis on the G-PEDOT:PSS films to see how the surface morphology of G-PEDOT:PSS layer influences the retention time properties was carried out. PMID:22524004

  4. Cadmium Telluride Solar Cells with PEDOT:PSS Back Contact

    NASA Astrophysics Data System (ADS)

    Mount, Michael; Duarte, Fernanda; Paudel, Naba; Yan, Yanfa; Wang, Weining

    Cadmium Telluride (CdTe) solar cell is one of the most promising thin film solar cells and its highest efficiency has reached 21%. To keep improving the efficiency of CdTe solar cells, a few issues need to be addressed, one of which is the back contact. The back contact of CdTe solar cells are mostly Cu-base, and the problem with Cu-based back contact is that Cu diffuses into the grain boundary and into the CdS/CdTe junction, causing degradation problem at high temperature and under illumination. To continue improving the efficiency of CdTe/CdS solar cells, a good ohmic back contact with high work function and long term stability is needed. In this work, we report our studies on the potential of conducting polymer being used as the back contact of CdTe/CdS solar cells. Conducting polymers are good candidates because they have high work functions and high conductivities, are easy to process, and cost less, meeting all the requirements of a good ohmic back contact for CdTe. In our studies, we used poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) with different conductivities and compared them with traditional Cu-based back contact. It was observed that the CdTe solar cell performance improves as the conductivity of the PEDOT:PSS increase, and the efficiency (9.1%) is approaching those with traditional Cu/Au back contact (12.5%). Cadmium Telluride Solar Cells with PEDOT:PSS Back Contact.

  5. Photo- and Electroluminescence of Substituted Divinyl Dibenzothiophene Sulfone

    NASA Astrophysics Data System (ADS)

    Samsonova, L. G.; Degtyarenko, K. M.; Kopylova, T. N.; Palatova, A. V.; Kukhta, A. V.

    2016-08-01

    The spectral properties of two substituted divinyl dibenzothiophene sulfone in solutions of tetrahydrofuran, polyvinylcarbazole films, and films obtained by thermal vacuum deposition are investigated. The ability of these compounds in thin-layer ITO/PEDOT:PSS/NPD/L/Ca/Al and ITO/PEDOT:PSS/PVK+L/Ca/Al structures (L denotes the examined luminophore) to emit radiation at applied voltage is investigated. It is shown that the spectra of photo- and electroluminescence in the film have a strong red shift of ~100 nm compared to the photoluminescence in solutions. It is suggested that radiation belongs to excimers.

  6. PSS Parameters Tuning Using Genetic Algorithm

    NASA Astrophysics Data System (ADS)

    Abdulrahim, M.; Almoula, Zakaria Fadl; Al-Hafid, Hafid

    2008-10-01

    Optimal tuning of power system stabilizer (PSS) parameters using genetic algorithm with single objective function is presented in this paper. A Single Machine Infinite Bus (SMIB) system is considered. The main objective of this research paper is to investigate the suitability of genetic algorithm for effective tuning of parameters of the power system stabilizer in a single machine infinite bus system. A conventional speed based lead-lag PSS is used. A simple and effective method of tuning the parameters of PSS is proposed which is posed as an optimization formulation by maximizing the damping of modes of oscillations of the SMIB system over a wide range of loading conditions and different system configurations. It is found that GA based PSS with single objective design shows improved dynamic performance over Conventional PSS over a wide range of operating conditions and different system parameters.

  7. Correlation between the fine structure of spin-coated PEDOT:PSS and the photovoltaic performance of organic/crystalline-silicon heterojunction solar cells

    NASA Astrophysics Data System (ADS)

    Funda, Shuji; Ohki, Tatsuya; Liu, Qiming; Hossain, Jaker; Ishimaru, Yoshihiro; Ueno, Keiji; Shirai, Hajime

    2016-07-01

    We investigated the relationship between the fine structure of spin-coated conductive polymer poly(3,4-ethylenedioxythiphene):poly(styrene sulfonate) (PEDOT:PSS) films and the photovoltaic performance of PEDOT:PSS crystalline-Si (PEDOT:PSS/c-Si) heterojunction solar cells. Real-time spectroscopic ellipsometry revealed that there were two different time constants for the formation of the PEDOT:PSS network. Upon removal of the polar solvent, the PEDOT:PSS film became optically anisotropic, indicating a conformational change in the PEDOT and PSS chain. Polarized Fourier transform infrared attenuated total reflection absorption spectroscopy and Raman spectroscopy measurements also indicated that thermal annealing promoted an in-plane π-conjugated Cα = Cβ configuration attributed to a thiophene ring in PEDOT and an out-of-plane configuration of -SO3 groups in the PSS chain with increasing composition ratio of oxidized (benzoid) to neutral (quinoid) PEDOT, Iqui/Iben. The highest power conversion efficiency for the spin-coated PEDOT:PSS/c-Si heterojunction solar cells was 13.3% for Iqui/Iben = 9-10 without employing any light harvesting methods.

  8. Morphology of PEDOT:PSS/SWCNT Composites: Insight into Carbon Nanotube Based Organic Thermoelectric Matrices

    NASA Astrophysics Data System (ADS)

    Etampawala, Thusitha; Tehrani, Mehran; Dadmun, Mark

    2015-03-01

    Carbon nanotube (CNT) loaded poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) nanocomposites are promising materials as the active layer in organic thermoelectric devices. Improvements in the thermoelectric performance of these nanocomposites have been hampered by the lack of an understanding of the correlation between thermo-electrical performance and morphology. In this study, the morphology of highly conducting single walled CNT/PEDOT:PSS nanocomposites were probed by small and ultra-small angle neutron scattering (SANS and USANS respectively) as a function of CNT loading (10wt%, 30wt% and 50wt%,), sonication duration to control the CNT dispersion, and presence and absence of ethylene glycol (EG) in the deposition solution of PEDOT:PSS. The morphology of these composites is currently being correlated to their thermo-electric performance. The SANS and USANS profiles were analyzed with the hierarchical Beaucage model. Further, the USANS data were fit to a two ellipsoidal form factor, which is consistent with the analysis of the USANS data by the Beaucage model and SEM results. These results reveal that the sonication duration and presence of EG effectively de-bundle the CNTs and disperse them in the PEDOT:PSS matrix.

  9. Surface analysis of the selective excimer laser patterning of a thin PEDOT:PSS film on flexible polymer films

    NASA Astrophysics Data System (ADS)

    Schaubroeck, David; De Smet, Jelle; Willems, Wouter; Cools, Pieter; De Geyter, Nathalie; Morent, Rino; De Smet, Herbert; Van Steenbeerge, Geert

    2016-07-01

    Fast patterning of highly conductive polymers like PEDOT:PSS (poly (3,4-ethylene dioxythiophene): polystyrene sulfonate) with lasers can contribute to the development of industrial production of liquid crystal displays on polymer foils. In this article, the selective UV laser patterning of a PEDOT:PSS film on flexible polymer films is investigated. Based on their optical properties, three polymer films are investigated: polyethylene terephthalate (PET), polymethyl methacrylate (PMMA) and cellulose triacetate (TAC). Ablation parameters for a 110 nm PEDOT:PSS film on these polymer films are optimized. A detailed study of the crater depth, topography and surface composition are provided using optical profilometry, scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS), respectively. The electrical insulation of the lines is measured and correlated to the crater analyses for different laser settings. Finally, potential ablation parameters for each of the polymer films are derived.

  10. Structural, morphological and optical properties of PEDOT:PSS/QDs nano-composite films prepared by spin-casting

    NASA Astrophysics Data System (ADS)

    Najeeb, Mansoor Ani; Abdullah, Shahino Mah; Aziz, Fakhra; Ahmad, Zubair; Rafique, Saqib; Wageh, S.; Al-Ghamdi, Ahmed A.; Sulaiman, Khaulah; Touati, Farid; Shakoor, R. A.; Al-Thani, N. J.

    2016-09-01

    This paper describes the structural, morphological and optical properties of the nano-composite of poly (3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) and quantum dots (QDs). The ZnSe and CdSe QDs have been synthesized, with the aid of Mercaptoacetic acid (MAA), by a colloidal method with an average size of ~5 to 7 nm. QDs have been embedded in PEDOT:PSS using a simple solution processing approach and has been deposited as thin films by spin coating technique. The QDs embedded PEDOT:PSS enhances the light absorption spectra of samples, prominently in terms of absorption intensity which may consequently improve sensitivity of the optoelectronic devices.

  11. Segmentation of conducting domains in PEDOT:PSS films induced by an additive for conductivity enhancement

    NASA Astrophysics Data System (ADS)

    Unuma, Takeya; Yoshikawa, Muneki; Nakamura, Arao; Kishida, Hideo

    2016-05-01

    We investigate the relationship between the morphology and in-plane conductivity of poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) films made from aqueous dispersions with/without ethylene glycol additive. Nanometer-scale current images of the films obtained using a conductive atomic-force microscope reveal that PEDOT-rich highly conducting domains are segmented into smaller ones — with the total area of these domains being nearly constant — for larger percentages of ethylene glycol leading to higher in-plane conductivities. The in-plane transport mechanism is found to have a strong dependence on the effective thickness of insulating barriers formed by excess PSS between neighboring highly conducting domains.

  12. A dye-sensitized solar cell based on natural photosensitizers and a PEDOT:PSS/TiO2 film as a counter electrode

    NASA Astrophysics Data System (ADS)

    Jafari, Fatemeh; Behjat, Abbas; Khoshroo, Ali R.; Ghoshani, Maral

    2015-02-01

    Poly(3, 4-ethylendioxythiophene)-poly(styrene sulfonate) mixed with TiO2 nanoparticles (PEDOT:PSS/TiO2) was used as a catalyst for tri-iodide reduction in dye-sensitized solar cells based on natural photosensitizers. A PEDOT:PSS/TiO2 film was coated on a conductive glass substrate by the spin coating method. The solar cells were fabricated, having the PEDOT:PSS/TiO2 film as a counter electrode and Pomegranate juice dye-sensitized TiO2 as an anode. The morphology of PEDOT:PSS/TiO2 films was studied by scanning electron microscopy (SEM) and atomic force microscopy (AFM) images. Cyclic voltammetry (CV) was employed to characterize the catalytic activity of the PEDOT:PSS/TiO2 film. Based on the analysis of CV, the enhancements for the electrochemical and photochemical performance of the PEDOT:PSS/TiO2 electrode are attributed to the fact that the dispersed TiO2 nanoparticles in the PEDOT:PSS matrix provide an improved catalytic activity and a facilitated diffusion for tri-iodide ions. The energy conversion efficiency is significantly improved after TiO2 nanoparticle incorporation. This improvement might be attributed to an increase in the counter electrode catalytic activity. The highest efficiency of 0.73% was obtained by using 100 nm TiO2 nanoparticles in the counter electrode.

  13. Improving the performance of perovskite solar cells with glycerol-doped PEDOT:PSS buffer layer

    NASA Astrophysics Data System (ADS)

    Jian-Feng, Li; Chuang, Zhao; Heng, Zhang; Jun-Feng, Tong; Peng, Zhang; Chun-Yan, Yang; Yang-Jun, Xia; Duo-Wang, Fan

    2016-02-01

    In this paper, we investigate the effects of glycerol doping on transmittance, conductivity and surface morphology of poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate)) (PEDOT:PSS) and its influence on the performance of perovskite solar cells. . The conductivity of PEDOT:PSS is improved obviously by doping glycerol. The maximum of the conductivity is 0.89 S/cm when the doping concentration reaches 6 wt%, which increases about 127 times compared with undoped. The perovskite solar cells are fabricated with a configuration of indium tin oxide (ITO)/PEDOT:PSS/CH3NH3PbI3/PC61BM/Al, where PEDOT:PSS and PC61BM are used as hole and electron transport layers, respectively. The results show an improvement of hole charge transport as well as an increase of short-circuit current density and a reduction of series resistance, owing to the higher conductivity of the doped PEDOT:PSS. Consequently, it improves the whole performance of perovskite solar cell. The power conversion efficiency (PCE) of the device is improved from 8.57% to 11.03% under AM 1.5 G (100 mW/cm2 illumination) after the buffer layer has been modified. Project supported by the National Natural Science Foundation of China (Grant Nos. 61264002, 61166002, 91333206, and 51463011), the Natural Science Foundation of Gansu Province, China (Grant No. 1308RJZA159), the New Century Excellent Talents in University of Ministry of Education of China (Grant No. NCET-13-0840), the Research Project of Graduate Teacher of Gansu Province, China (Grant No. 2014A-0042), and the Postdoctoral Science Foundation from Lanzhou Jiaotong University, China.

  14. Destructive effect of polystyrene sulfonate on the structure of hemoproteins

    NASA Astrophysics Data System (ADS)

    Saburova, E. A.; Basova, L. V.; Dybovskaya, Yu. N.; Sukhorukov, B. I.

    2006-08-01

    The mechanism of the destruction of horse heart hemoglobin (Hb) and spermwhale muscle myoglobin (Mb), two hem-containing proteins, by polystyrene sulfonate, an anionic polyelectrolyte, was studied. Measurements of the optical absorption of the prostetic group of the hem in the visible spectrum and of the circular dichroism in the absorption bands of the peptide groups and aromatic amino acid residues demonstrated that the compact structure of both proteins experiences destruction in the presence of polystyrene sulfonate (PSS) at PSS concentrations ten times as low as that of the protein (in wt %) and that the content of α-helix structure in Hb and Mb decreases from 81% in the native state to 43% in their complexes with PSS. The distinctions in the mechanisms of the destruction of Hb and Mb by PSS were found to be as follows: (1) in contrast to Mb, Hb forms insoluble complexes with PSS at low PSS concentrations and (2) Mb-PSS solutions at Mb-to-PSS ratios >1 were found to contain free hems (that absorb at 397 nm), a feature not observed for Hb; the kinetics of the destruction of both the proteins by the polyelectrolyte was demonstrated to be a two-stage process. The first stage of the destruction of Hb (τ ≈ 24.5 s) was found to be four times as slow as that of Mb (τ ≈ 6 s); the second (slow) stage had a halftime of ˜6 h for both the proteins under study. To determine the localization of regions at the protein molecule surface that are capable of binding polyelectrolyte molecules, the distribution of the electrostatic potential over the surface of the Hb and Mb molecules was numerically calculated with the help of the Poisson-Boltzmann equation at pH 6.2 and an ionic strength of 100 mmol/l. Based on experimental and theoretical studies of the mechanism of the interaction of the polyelectrolyte with the proteins, the structural-functional properties of proteins responsible for their destruction by the polyelectrolyte are determined.

  15. Predictive optimized adaptive PSS in a single machine infinite bus.

    PubMed

    Milla, Freddy; Duarte-Mermoud, Manuel A

    2016-07-01

    Power System Stabilizer (PSS) devices are responsible for providing a damping torque component to generators for reducing fluctuations in the system caused by small perturbations. A Predictive Optimized Adaptive PSS (POA-PSS) to improve the oscillations in a Single Machine Infinite Bus (SMIB) power system is discussed in this paper. POA-PSS provides the optimal design parameters for the classic PSS using an optimization predictive algorithm, which adapts to changes in the inputs of the system. This approach is part of small signal stability analysis, which uses equations in an incremental form around an operating point. Simulation studies on the SMIB power system illustrate that the proposed POA-PSS approach has better performance than the classical PSS. In addition, the effort in the control action of the POA-PSS is much less than that of other approaches considered for comparison.

  16. Fabrication of novel two-dimensional nanopatterned conductive PEDOT:PSS films for organic optoelectronic applications.

    PubMed

    Petti, Lucia; Rippa, Massimo; Capasso, Rossella; Nenna, Giuseppe; De Girolamo Del Mauro, Anna; Pandolfi, Giuseppe; Maglione, Maria Grazia; Minarini, Carla

    2013-06-12

    This paper presents a novel strategy to fabricate two-dimensional poly(3,4 ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) photonic crystals (PCs) combining electron beam lithography (EBL) and plasma etching (PE) processes. The surface morphology of PEDOT:PSS PCs after mild oxygen plasma treatment was investigated by scanning electron microscopy. The effects on light extraction are studied experimentally. Vertical extraction of light was found to be strongly dependent on the geometric parameters of the PCs. By changing the lattice type from triangular to square and the geometrical parameters of the photonic structures, the resonance peak could be tuned from a narrow blue emission at 445 nm up to a green emission at 525 nm with a full width at half-maximum of 20 nm, which is in good agreement with Bragg's diffraction theory and free photon band structure. Both finite-difference time-domain and plane wave expansion methods are used to calculate the resonant frequencies and the photonic band structures in the two-dimensional photonic crystals showing a very good agreement with the experiment results. A 2D nanopatterned transparent anode was also fabricated onto a flexible polyethylene terephthalate (PET) substrate and it was integrated into an organic light-emitting diode (OLED). The obtained results fully confirm the feasibility of the developed process of micro/nano patterning PEDOT:PSS. Engineered polymer electrodes prepared by this unique method are useful in a wide variety of high-performance flexible organic optoelectronics.

  17. Junction formation and current transport mechanisms in hybrid n-Si/PEDOT:PSS solar cells

    NASA Astrophysics Data System (ADS)

    Jäckle, Sara; Mattiza, Matthias; Liebhaber, Martin; Brönstrup, Gerald; Rommel, Mathias; Lips, Klaus; Christiansen, Silke

    2015-08-01

    We investigated hybrid inorganic-organic solar cells combining monocrystalline n-type silicon (n-Si) and a highly conductive polymer poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate) (PEDOT:PSS). The build-in potential, photo- and dark saturation current at this hybrid interface are monitored for varying n-Si doping concentrations. We corroborate that a high build-in potential forms at the hybrid junction leading to strong inversion of the n-Si surface. By extracting work function and valence band edge of the polymer from ultraviolet photoelectron spectroscopy, a band diagram of the hybrid n-Si/PEDOT:PSS heterojunction is presented. The current-voltage characteristics were analyzed using Schottky and abrupt pn-junction models. The magnitude as well as the dependence of dark saturation current on n-Si doping concentration proves that the transport is governed by diffusion of minority charge carriers in the n-Si and not by thermionic emission of majorities over a Schottky barrier. This leads to a comprehensive explanation of the high observed open-circuit voltages of up to 634 mV connected to high conversion efficiency of almost 14%, even for simple planar device structures without antireflection coating or optimized contacts. The presented work clearly shows that PEDOT:PSS forms a hybrid heterojunction with n-Si behaving similar to a conventional pn-junction and not, like commonly assumed, a Schottky junction.

  18. Junction formation and current transport mechanisms in hybrid n-Si/PEDOT:PSS solar cells

    PubMed Central

    Jäckle, Sara; Mattiza, Matthias; Liebhaber, Martin; Brönstrup, Gerald; Rommel, Mathias; Lips, Klaus; Christiansen, Silke

    2015-01-01

    We investigated hybrid inorganic-organic solar cells combining monocrystalline n-type silicon (n-Si) and a highly conductive polymer poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate) (PEDOT:PSS). The build-in potential, photo- and dark saturation current at this hybrid interface are monitored for varying n-Si doping concentrations. We corroborate that a high build-in potential forms at the hybrid junction leading to strong inversion of the n-Si surface. By extracting work function and valence band edge of the polymer from ultraviolet photoelectron spectroscopy, a band diagram of the hybrid n-Si/PEDOT:PSS heterojunction is presented. The current-voltage characteristics were analyzed using Schottky and abrupt pn-junction models. The magnitude as well as the dependence of dark saturation current on n-Si doping concentration proves that the transport is governed by diffusion of minority charge carriers in the n-Si and not by thermionic emission of majorities over a Schottky barrier. This leads to a comprehensive explanation of the high observed open-circuit voltages of up to 634 mV connected to high conversion efficiency of almost 14%, even for simple planar device structures without antireflection coating or optimized contacts. The presented work clearly shows that PEDOT:PSS forms a hybrid heterojunction with n-Si behaving similar to a conventional pn-junction and not, like commonly assumed, a Schottky junction. PMID:26278010

  19. Silver nanoparticles functionalized in situ with the conjugated polymer (PEDOT:PSS).

    PubMed

    Moreno, Karla J; Moggio, Ivana; Arias, Eduardo; Llarena, Irantzu; Moya, Sergio E; Ziolo, Ronald F; Barrientos, Hector

    2009-06-01

    Silver nanoparticles have been functionalized in situ with the electrically conducting polymer, poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate) (PEDOT:PSS) via colloidal synthesis. The formation of the functionalized silver nanoparticles, hereafter designated Ag(PEDOT:PSS), was confirmed by the appearance of the characteristic plasmon absorption peak at 420 nm in the UV-Vis spectrum of the aqueous suspension and by TEM analysis, where spherical particles with a mean size of around 8 nm (metallic core) were observed. Homogeneous thin films with granular topography, as observed by AFM, were prepared by self assembly. Electrical studies of the films showed an increase in electrical conductivity of three orders of magnitude with respect to the polymer film presumably due to the presence of the silver core. The conductive polymer/silver composite films also exhibit interesting electrochromic switching between blue and brown. These properties suggest the possibility of a variety of applications of Ag(PEDOT:PSS) films such as in electro optics devices, smart windows, amperometric sensors and capacitors.

  20. Thermoelectric Power-Generation Characteristics of PEDOT:PSS Thin-Film Devices with Different Thicknesses on Polyimide Substrates

    NASA Astrophysics Data System (ADS)

    Anno, Hiroaki; Nishinaka, Takahiko; Hokazono, Masahiro; Oshima, Nobuaki; Toshima, Naoki

    2015-06-01

    We fabricated cast films of complexes of poly(3,4-ethylenedioxythiophene) and polystyrene sulfonic acid (PEDOT:PSS) at various thicknesses, t = 3-20 μm, on flexible polyimide substrates, and studied their thermoelectric properties. We also fabricated in-plane film devices consisting of five couples of PEDOT:PSS and Ag electrodes, measuring their output power characteristics as a function of film thickness. The Seebeck coefficient and electrical conductivity of a PEDOT:PSS film with a thickness of ˜20 μm on a polyimide substrate were ˜15 μV/K and 500 S/cm, respectively, near room temperature. As the film thickness decreased from ˜10 μm to 3 μm, the electrical conductivity increased remarkably to 1200 S/cm, while the Seebeck coefficient remained almost constant with film thickness. The maximum electric power for an in-plane PEDOT:PSS film device with a thickness of 10 μm was 1.3 μW at Δ T = 100 K. Its open-circuit voltage was 7.3 mV, and its internal resistance was 11 Ω. The measured power-generation characteristics of the film device agreed with values estimated from the dependence of thermoelectric properties on film thickness for PEDOT:PSS films on polyimide substrates. Assuming single PEDOT:PSS legs, defined as the direction of heat transport, we estimated the expected electrical power density at Δ T = 100 K as ˜650 μW/cm2 for a film thickness t = 10 μm, and 1400 μW/cm2 for t = 3 μm.

  1. Characterization of free-standing PEDOT:PSS/iron oxide nanoparticle composite thin films and application as conformable humidity sensors.

    PubMed

    Taccola, Silvia; Greco, Francesco; Zucca, Alessandra; Innocenti, Claudia; Fernández, César de Julián; Campo, Giulio; Sangregorio, Claudio; Mazzolai, Barbara; Mattoli, Virgilio

    2013-07-10

    In this study, a new simple, fast, and inexpensive technique for the preparation of free-standing nanocomposite ultrathin films based on the conductive polymer poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) and embedding iron oxide nanoparticles (NPs) is presented. These nanofilms were fabricated by a single step of spin-coated assisted deposition in conjunction with a release technique ("supporting layer technique") to detach them from the substrate. Free-standing nanofilms can be easily transferred onto several substrates due to their high conformability, preserving their functionalities. The effect of the addition of iron oxide nanoparticles on the structural and functional properties of the PEDOT:PSS nanofilms is investigated through topography, thickness, magnetic, magneto-optical activity, and conductivity characterizations. PEDOT:PSS and PEDOT:PSS/iron oxide NP nanofilms were tested as resistive humidity sensors. Their sensitivity to humidity was found to increase with increasing nanoparticle concentration. On the basis of these results, it is expected that these composites may furnish inexpensive and reliable means for relative humidity detection. PMID:23802632

  2. Graphene oxide/PEDOT:PSS composite hole transport layer for efficient and stable planar heterojunction perovskite solar cells

    NASA Astrophysics Data System (ADS)

    Lee, Da-Young; Na, Seok-In; Kim, Seok-Soon

    2016-01-01

    We investigated a graphene oxide (GO)/poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) composite as a promising candidate for the practical application of a 2-D carbonaceous hole transport layer (HTL) to planar heterojunction perovskite solar cells (PeSCs) consisting of a transparent electrode/HTL/perovskite/fullerene/metal electrode. Both the insulating properties of GO and the non-uniform coating of the transparent electrode with GO cause the poor morphology of perovskite induced low power conversion efficiency (PCE) of 6.4%. On the other hand, PeSCs with a GO/PEDOT:PSS composite HTL, exhibited a higher PCE of 9.7% than that of a device fabricated with conventional PEDOT:PSS showing a PCE of 8.2%. The higher performance is attributed to the decreased series resistance (RS) and increased shunt resistance (RSh). The well-matched work-function between GO (4.9 eV) and PEDOT:PSS (5.1 eV) probably results in more efficient charge transport and an overall decrease in RS. The existence of GO with a large bandgap of ~3.6 eV might induce the effective blocking of electrons, leading to an increase of RSh. Moreover, improvement in the long-term stability under atmospheric conditions was observed.

  3. Ion-beam-spurted dimethyl-sulfate-doped PEDOT:PSS composite-layer-aligning liquid crystal with low residual direct-current voltage

    NASA Astrophysics Data System (ADS)

    Liu, Yang; Lee, Ju Hwan; Seo, Dae-Shik; Li, Xiang-Dan

    2016-09-01

    Thin ion-beam (IB)-spurted dimethyl sulfate/poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (DMS/PEDOT:PSS) layers with improved electro-optic performance are presented for aligning liquid crystals. IB spurting is effective for enhancing the conductivity of such layers, as well as the anchoring energy of the liquid crystals sandwiched between them. Compared with a commercial twisted-nematic cell assembled with polyimide alignment layers, the same cell assembled with 3.0-keV IB-spurted DMS/PEDOT:PSS alignment layers shows a 38% faster switching and a 93% lower residual direct current. The improved electro-optic performance here is likely due to the enhanced electric field effect and the charge-releasing ability of thin IB-spurted DMS/PEDOT:PSS layers.

  4. A highly conductive poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) film with the solvent bath treatment by dimethyl sulfoxide as cathode for polymer tantalum capacitor

    NASA Astrophysics Data System (ADS)

    Ma, Xiaopin; Wang, Xiuyu; Li, Mingxiu; Chen, Tongning; Zhang, Hao; Chen, Qiang; Ding, Bonan; Liu, Yanpeng

    2016-06-01

    The highly conductive poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) films were prepared on porous tantalum pentoxide surface as cathode for polymer tantalum capacitors (PTC). The electrical performances of PTC with PEDOT:PSS films as cathode were optimized by dimethyl sulfoxide (DMSO) bath treatment. With the DMSO-bath treatment of PTC, the equivalent series resistance (ESR) of PTC decreased from 25 mΩ to 9 mΩ. The ultralow ESR led to better capacitance-frequency performance. The device reliability investigation revealed the enhanced environmental stability of PTC. The enhanced performances were attributed to the conductivity improvement of PEDOT:PSS cathode films and the removal of excess PSS from PEDOT:PSS films.

  5. Sulfonated polyphenylene polymers

    DOEpatents

    Cornelius, Christopher J.; Fujimoto, Cy H.; Hickner, Michael A.

    2007-11-27

    Improved sulfonated polyphenylene compositions, improved polymer electrolyte membranes and nanocomposites formed there from for use in fuel cells are described herein. The improved compositions, membranes and nanocomposites formed there from overcome limitations of Nafion.RTM. membranes.

  6. Sodium Polystyrene Sulfonate

    MedlinePlus

    ... is used to treat hyperkalemia (increased amounts of potassium in the body). Sodium polystyrene sulfonate is in a class of medications called potassium-removing agents. It works by removing excess potassium ...

  7. Sensitive and selective turn-on fluorescence method for cetyltrimethylammonium bromide determination based on acridine orange-polystyrene sulfonate complex.

    PubMed

    Li, Na; Hao, Xia; Kang, Bei Hua; Li, Nian Bing; Luo, Hong Qun

    2016-06-01

    This work proposed a rapid and novel fluorescence-sensing system using a complex of acridine orange (AO) and polystyrene sulfonate (PSS) to sensitively recognize and monitor cetyltrimethylammonium bromide (CTAB) in an aqueous medium. AO can interact with PSS and a complex is formed via electrostatic attraction and hydrophobic interaction. The fluorescence of AO is greatly quenched after the introduction of PSS. Upon its subsequent addition, CTAB can interact and form a complex with PSS because the electrostatic attraction between CTAB and PSS is much stronger than that between AO and PSS, which results in significant fluorescence recovery. Interestingly, the proposed method can be applied for the discrimination and detection of surfactants with different hydrocarbon chain lengths due to their different binding affinity toward PSS. The detection limit for CTAB is as low as 0.2 µg/mL and the linear range is from 0.5 to 3.5 µg/mL. Moreover, we applied the sensor to the successful detection of CTAB in water samples. Copyright © 2015 John Wiley & Sons, Ltd.

  8. Cross-linked polystyrene sulfonic acid and polyethylene glycol as a low-fouling material.

    PubMed

    Alghunaim, Abdullah; Zhang Newby, Bi-min

    2016-04-01

    A negatively charged hydrophilic low fouling film was prepared by thermally cross-linking a blend consisting of polystyrene sulfonic acid (PSS) and polyethylene glycol (PEG). The film was found to be stable by dip-washing. The fouling resistance of this material toward bacterial (Escherichia coli) and colloidal (polystyrene particles) attachment, non-specific protein (fibronectin) adsorption and cell (3T3 NIH) adhesion was evaluated and was compared with glass slides modified with polyethylene glycol (PEG) brushes, oxidized 3-mercaptopropyltrimethoxysilane (sulfonic acid, SA), and n-octadecyltrichlorosilane (OTS). The extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) theory and thermodynamic models based on surface energy were used to explain the interaction behaviors of E. coli/polystyrene particles-substrate and protein-substrate interactions, respectively. The cross-linked PSS-PEG film was found to be slightly better than SA and PEG toward resisting non-specific protein adsorption, and showed comparable low attachment results as those of PEG toward particle, bacterial and NIH-3T3 cells adhesion. The low-fouling performance of PSS-PEG, a cross-linked film by a simple thermal curing process, could allow this material to be used for applications in aqueous environments, where most low fouling hydrophilic polymers, such as PSS or PEG, could not be easily retained.

  9. Electrical and Morphological Properties of Inkjet Printed Pedot/PSS Films

    SciTech Connect

    Garnett, E.; Ginley, D.

    2005-01-01

    Organic solar cells and LEDs are becoming more popular because their low cost materials, potential manufacturability, and recent gains in efficiency make them feasible for widespread commercialization in the near future. One significant manufacturing problem, especially for OLEDs, is the cost associated with creating patterned devices with spatially non-specific deposition methods such as spincoating. Inkjet printing can remove this problem. In recent years, inkjet printed polyethylene(3,4-dioxythiophene)/ polystyrene sulfonate (PEDOT/PSS) has been incorporated into many organic devices to help charge transfer, but there has not been much research regarding the effect of different printing parameters on the electrical and morphological film properties. In this work, an atomic force microscope, four point probe, and Kelvin probe were used to study the effects of printing parameters on roughness, conductivity and workfunction. Inkjet printed PEDOT films were also compared to spincoated films to determine how the polymer deposition method affects the above properties. Generally, inkjet printing created rougher but more conductive films with a smaller workfunction. Additionally, it was demonstrated that the workfunction of PEDOT films could be tuned over a range of about 0.5 V by changing the solvent mixture or substrate surface pretreatment. All additives to the as received PEDOT/PSS suspension caused the workfunction to decrease. It was discovered that workfunction decreases as printing voltage increases, but the trend reverses after annealing the films. This phenomenon suggests that when DMSO interacts with PEDOT, the workfunction changes. Finally, the results support previous publications suggesting that DMSO increases conductivity through a screening effect and also by changing the distribution of PEDOT and PSS in the film.

  10. Humidity Sensor Based on PEDOT:PSS and Zinc Stannate Nano-composite

    NASA Astrophysics Data System (ADS)

    Aziz, Shahid; Chang, Dong Eui; Doh, Yang Hoi; Kang, Chul Ung; Choi, Kyung Hyun

    2015-10-01

    A composite of poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) and zinc stannate (ZnSnO3) has been introduced for impedance-based humidity sensing, owing to its high sensitivity, good stability, very fast response (˜0.2 s) and recovery time (˜0.2 s), small hysteresis, repeatability, low-cost fabrication and wide range of sensitivity. Both materials were mixed in three different weight percentage ratios, to optimize the performance of the sensors. Best response was observed for 5 wt.% PEDOT:PSS and 5 wt.% ZnSnO3. The impedance of the sensor was dropped immensely from 1.5 MΩ to 50 kΩ by changing relative humidity from 0% to 90%. The reason for this improvement in sensitivity was analyzed by virtue of sensing mechanisms and different characterizations (three dimensional (3D) nano-profiler, optical microscope, and fourier transform infra-red (FTIR) spectroscopy) revealing the surface morphology and chemical structure of the film. Due to its response and ability to sense human breath and skin humidity, it is suitable for environmental, artificial skin and food industry applications.

  11. Low Work-function Poly(3,4-ethylenedioxylenethiophene): Poly(styrene sulfonate) as Electron-transport Layer for High-efficient and Stable Polymer Solar Cells

    PubMed Central

    Zhang, Yong; Chen, Lie; Hu, Xiaotian; Zhang, Lin; Chen, Yiwang

    2015-01-01

    Low-work-function poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) modified with polyethylenimine (PEIE) was used as an electron transport layer (ETL) for polymer solar cells (PSCs). A thin layer of PEIE film was spin-coated onto the surface on the PEDOT:PSS films, thus substantially changing their charge selectivity from supporting hole transport to supporting electron transport. It was also found that the PEDOT:PSS/PEIE ETL exhibited higher interfacial contact, a more favorable active morphology, and improved charge mobility. By virtue of these beneficial properties, inverted PSCs based on low-bandgap semiconducting photoactive layers achieved a notably improved power conversion efficiency (PCE) of 7.94%, superior even to the corresponding performance of devices with only a ZnO layer. Surpassing our expectations, compared with the extreme degradation of device stability observed when pure PEDOT:PSS is used, PEIE-modified PEDOT:PSS can considerably suppress device degradation because of the hydrophobic and alkaline nature of PEIE, which not only reduces the hygroscopicity of the PEDOT:PSS but also neutralizes the acidic PEDOT:PSS and thus prevents the corrosion of the ITO cathode. These results demonstrate the potential of PEIE-modified PEDOT:PSS for use as an efficient ETL in commercial printed electronic devices. PMID:26239868

  12. Modification of conductive polymer PEDOT:PSS layer by SWCNT

    NASA Astrophysics Data System (ADS)

    Araźna, Aneta; Janeczek, Kamil; Futera, Konrad; Koziol, Andrzej

    2016-01-01

    In this study, the effect of addition of single-walled carbon nanotubes (SWCNTs) on the morphological properties of poly(3,4-ethylenedioxythiophene/poly(4-styrenesulfonate) (PEDOT:PSS) has been investigated using scanning electron microscope (SEM) as well as the surface roughness evaluation by atomic force microscopy (AFM). The spin-coated films of PEDOT:PSS and PEDOT:PSS with addition of SWNTs (0.5 % by wt.) on glass were compared in our study. Experimental results show that surface roughness of PEDOT:PSS layers increases after addition SWNTs to the solution - from 3.50 nm for the samples without SWNTs to 4.65 nm for the samples with SWNTs. The analysis of SEM images showed that there are some agglomerations of SWNTs on the surface of PEDOT:PSS/SWCNT composite film.

  13. PEDOT:PSS Interfaces Support the Development of Neuronal Synaptic Networks with Reduced Neuroglia Response In vitro

    PubMed Central

    Cellot, Giada; Lagonegro, Paola; Tarabella, Giuseppe; Scaini, Denis; Fabbri, Filippo; Iannotta, Salvatore; Prato, Maurizio; Salviati, Giancarlo; Ballerini, Laura

    2016-01-01

    The design of electrodes based on conductive polymers in brain-machine interface technology offers the opportunity to exploit variably manufactured materials to reduce gliosis, indeed the most common brain response to chronically implanted neural electrodes. In fact, the use of conductive polymers, finely tailored in their physical-chemical properties, might result in electrodes with improved adaptability to the brain tissue and increased charge-transfer efficiency. Here we interfaced poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) doped with different amounts of ethylene glycol (EG) with rat hippocampal primary cultures grown for 3 weeks on these synthetic substrates. We used immunofluorescence and scanning electron microscopy (SEM) combined to single cell electrophysiology to assess the biocompatibility of PEDOT:PSS in terms of neuronal growth and synapse formation. We investigated neuronal morphology, density and electrical activity. We reported the novel observation that opposite to neurons, glial cell density was progressively reduced, hinting at the ability of this material to down regulate glial reaction. Thus, PEDOT:PSS is an attractive candidate for the design of new implantable electrodes, controlling the extent of glial reactivity without affecting neuronal viability and function. PMID:26834546

  14. Characterization of Piezoresistive PEDOT:PSS Pressure Sensors with Inter-Digitated and Cross-Point Electrode Structures

    PubMed Central

    Wang, Jer-Chyi; Karmakar, Rajat Subhra; Lu, Yu-Jen; Huang, Chiung-Yin; Wei, Kuo-Chen

    2015-01-01

    The piezoresistive characteristics of poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) pressure sensors with inter-digitated (IDE) and cross-point electrode (CPE) structures have been investigated. A small variation of the resistance of the pressure sensors with IDE without bottom indium-tin-oxide (b-ITO) film and with CPE structures was observed owing to the single carrier-conducting pathway. For the IDE pressure sensors with b-ITO, the piezoresistive characteristics at low and high pressure were similar to those of the pressure sensors with IDE without b-ITO and with CPE structures, respectively, leading to increased piezoresistive pressure sensitivity as the PEDOT:PSS film thickness decreased. A maximum sensitivity of more than 42 kΩ/Pa was achieved. When the normal pressure was applied, the increased number of conducting points or the reduced distance between the PEDOT oligomers within the PEDOT:PSS film resulted in a decrease of the resistance. The piezoresistive pressure sensors with a single carrier-conducting pathway, i.e., IDE without b-ITO and CPE structures, exhibited a small relaxation time and a superior reversible operation, which can be advantageous for fast piezoresistive response applications. PMID:25569756

  15. PEDOT/PSS-Halloysite Nanotubes (HNTs) Hybrid Films: Insulating HNTs Enhance Conductivity of the PEDOT/PSS Films

    NASA Astrophysics Data System (ADS)

    Yan, Hu; Zhang, Ping; Li, Juan; Zhao, Xiao-Li; Zhang, Ke; Zhang, Bing

    2015-12-01

    We have for the first time found that completely insulating Halloysite nanotubes (HNTs) significantly enhance electrical conductivity of PEDOT/PSS films by simply mixing. Based on this accident finding we have created highly porous and conductive PEDOT/PSS films hybridized with the HNTs. Through further optimization of the mixing condition we have obtained flexible and conductive hybrid films with high specific surface area. Based on experimental evidences we proposed a plausible mechanism of the phenomenon where the PEDOT/PSS colloidal particle with particle size of several tens nanometers well pack at the nano-channels into well-ordered structures of PEDOT/PSS particles, which show conductivity as higher as several order of magnitude than that of PEDOT/PSS particles in outside of the HNTs.

  16. Improved performance of poly(3,4-ethylenedioxythiophene):poly(stylene sulfonate)/n-Si hybrid solar cell by incorporating silver nanoparticles

    NASA Astrophysics Data System (ADS)

    Khatri, Ishwor; Liu, Qiming; Ueno, Keiji; Shirai, Hajime

    2014-11-01

    We report an enhancement in the efficiency of poly(3,4-ethylenedioxythiophene):poly(stylene sulfonate) (PEDOT:PSS)/n-Si hybrid solar cell by incorporating silver nanoparticles (AgNPs) with PEDOT:PSS. AgNPs were prepared by reducing silver nitrate in green-tea solution, which showed characteristic absorption peak due to the surface plasmonic resonance effect. AgNPs incorporated PEDOT:PSS/n-Si hybrid device shows power conversion efficiency (η) of 10.21%, which is comparatively higher to the performance of pristine device without AgNPs. Here, we noticed that incorporation of AgNPs decreases sheet resistance and enlarged surface roughness of PEDOT:PSS film for the efficient collection of charges, rather than plasmonic effect.

  17. Electrodeposition of manganese dioxide in three-dimensional poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonic acid)-polyaniline for supercapacitor

    NASA Astrophysics Data System (ADS)

    Liu, Feng-Jiin

    The preparation of composites of precise metal oxides/conducting polymers is important in studies of supercapacitors. In this work, a three-dimensional matrix of poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonic acid)-polyaniline (PEDOT-PSS-PANI) was prepared by interfacial polymerization of ANI into PEDOT-PSS. Conductivity was enhanced by incorporating of PANI into PEDOT-PSS because of the decrease in the distance for electron shuttling along the conjugated polymeric chain. Composite electrodes were prepared by the electrodeposition of manganese dioxide (MnO 2) in a PEDOT-PSS-PANI three-dimensional matrix. The electrodes were characterized by field emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS), and cyclic voltammetry techniques. The results show a significant improvement in the specific capacitance of the composite electrode. For PEDOT-PSS the specific capacitance was of 0.23 F g -1, while PEDOT-PSS-PANI and PEDOT-PSS-PANI-MnO 2 displayed values of 6.7 and 61.5 F g -1, respectively. When only considering the MnO 2 mass, the composite had the specific capacitance of 372 F g -1. The composite also had an excellent cyclic performance.

  18. Interaction between cationic surfactant of 1-methyl-3-tetradecylimidazolium bromide and anionic polymer of sodium polystyrene sulfonate

    NASA Astrophysics Data System (ADS)

    Zhang, Qian; Kang, Wenpei; Sun, Dezhi; Liu, Jie; Wei, Xilian

    2013-08-01

    The interaction between long-chain imidazolium ionic liquid (C14mimBr) and anionic polyelectrolyte of sodium polystyrene sulfonate (NaPSS) has been studied using surface tension, isothermal titration microcalorimetry (ITC), dynamic light scatting (DLS) and conductance methods. The result shows that the surface tension plots have a pronounced hump in the surface tension at surfactant concentrations below the critical micelle concentration (cmc) of the surfactant. The cooperative adsorption of surfactant and polymer on the surface (PSS) and the formation of polymer/surfactant aggregate in bulk solution (PSM) provide a rational explanation about it. The formation of surfactant/polymer complexes is affected by the concentration of the surfactant or NaPSS, which is also ascertained by ITC and DLS measurements. Further, the thermodynamic parameters are derived from calorimetric titration and conductance curves, and the effects of polymer concentration and temperature on the parameters are evaluated in detail.

  19. Super-fast switching of liquid crystals sandwiched between highly conductive graphene oxide/dimethyl sulfate doped PEDOT:PSS composite layers

    NASA Astrophysics Data System (ADS)

    Liu, Yang; Zhang, Yifan; Oh, Byeong-Yun; Seo, Dae-Shik; Li, Xiangdan

    2016-05-01

    Graphene oxide (GO)-doped dimethyl sulfate (DMS)/poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) superconductive alignment layer, aligning liquid crystals (LCs) with super switching and non-residual direct current (non-residual DC) performance, is presented in this manuscript. Doping of GO increased the pristine polar energy of a thin composite layer as well as the corresponding anchoring energy of the LCs sandwiched between these thin layers but only slightly affected the thin layers' morphology. When rubbed GO/DMS/PEDOT:PSS composite layers were used as alignment layers, a homogeneous alignment of nematic LCs was observed with competitive optoelectrical switching properties and non-residual DC performance because of the enhanced field effect and charge transport induced by the doped GO.

  20. Enhancement of Thermoelectric Properties of PEDOT:PSS and Tellurium-PEDOT:PSS Hybrid Composites by Simple Chemical Treatment

    NASA Astrophysics Data System (ADS)

    Jin Bae, Eun; Hun Kang, Young; Jang, Kwang-Suk; Yun Cho, Song

    2016-01-01

    The thermoelectric properties of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) and tellurium-PEDOT:PSS (Te-PEDOT:PSS) hybrid composites were enhanced via simple chemical treatment. The performance of thermoelectric materials is determined by their electrical conductivity, thermal conductivity, and Seebeck coefficient. Significant enhancement of the electrical conductivity of PEDOT:PSS and Te-PEDOT:PSS hybrid composites from 787.99 and 11.01 to 4839.92 and 334.68 S cm-1, respectively was achieved by simple chemical treatment with H2SO4. The power factor of the developed materials could be effectively tuned over a very wide range depending on the concentration of the H2SO4 solution used in the chemical treatment. The power factors of the developed thermoelectric materials were optimized to 51.85 and 284 μW m-1 K-2, respectively, which represent an increase of four orders of magnitude relative to the corresponding parameters of the untreated thermoelectric materials. Using the Te-PEDOT:PSS hybrid composites, a flexible thermoelectric generator that could be embedded in textiles was fabricated by a printing process. This thermoelectric array generates a thermoelectric voltage of 2 mV using human body heat.

  1. Enhancement of Thermoelectric Properties of PEDOT:PSS and Tellurium-PEDOT:PSS Hybrid Composites by Simple Chemical Treatment

    PubMed Central

    Jin Bae, Eun; Hun Kang, Young; Jang, Kwang-Suk; Yun Cho, Song

    2016-01-01

    The thermoelectric properties of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) and tellurium-PEDOT:PSS (Te-PEDOT:PSS) hybrid composites were enhanced via simple chemical treatment. The performance of thermoelectric materials is determined by their electrical conductivity, thermal conductivity, and Seebeck coefficient. Significant enhancement of the electrical conductivity of PEDOT:PSS and Te-PEDOT:PSS hybrid composites from 787.99 and 11.01 to 4839.92 and 334.68 S cm−1, respectively was achieved by simple chemical treatment with H2SO4. The power factor of the developed materials could be effectively tuned over a very wide range depending on the concentration of the H2SO4 solution used in the chemical treatment. The power factors of the developed thermoelectric materials were optimized to 51.85 and 284 μW m−1 K−2, respectively, which represent an increase of four orders of magnitude relative to the corresponding parameters of the untreated thermoelectric materials. Using the Te-PEDOT:PSS hybrid composites, a flexible thermoelectric generator that could be embedded in textiles was fabricated by a printing process. This thermoelectric array generates a thermoelectric voltage of 2 mV using human body heat. PMID:26728992

  2. Colorful Polyelectrolytes: An Atom Transfer Radical Polymerization Route to Fluorescent Polystyrene Sulfonate.

    PubMed

    Huberty, Wayne; Tong, Xiaowei; Balamurugan, Sreelatha; Deville, Kyle; Russo, Paul S; Zhang, Donghui

    2016-03-01

    A labeled green fluorescent polystyrene sulfonate (LNaPSS) has been synthesized using atom transfer radical polymerization of a styrene sulfonate monomer with a fluorescent co-monomer, fluorescein thiocyanate-vinyl aniline. As a result this 100 % sulfonated polymer contains no hydrophobic patches along the chain backbone besides the fluorescent marker itself. The concentration of the fluorescent monomer was kept low to maintain the characteristic properties of the anionic polyelectrolyte, LNaPSS. ATRP conditions facilitated the production of polymers spanning a range of molecular weights from 35,000 to 175,000 in gram-scale batches with polydispersity indices of 1.01-1.24. Molecular weight increased with the monomer to initiator ratio. Gel permeation chromatography results show a unimodal distribution, and the polymer structure was also confirmed by (1)H NMR and FT-IR spectroscopy. Fluorescence spectroscopy confirmed covalent bonding of fluorescein isothiocyanate to the polymer, indicating that the polymer is suitable as a probe in fluorescence microscopy. To demonstrate this ability, the polymer was used to locate structural features in salt crystals formed during drying, as in the evaporation of sea mist. A second application to probe diffusion studies is also demonstrated. PMID:26745991

  3. Probing the PEDOT:PSS/cell interface with conductive colloidal probe AFM-SECM

    NASA Astrophysics Data System (ADS)

    Knittel, P.; Zhang, H.; Kranz, C.; Wallace, G. G.; Higgins, M. J.

    2016-02-01

    Conductive colloidal probe Atomic Force-Scanning Electrochemical Microscopy (AFM-SECM) is a new approach, which employs electrically insulated AFM probes except for a gold-coated colloid located at the end of the cantilever. Hence, force measurements can be performed while biasing the conductive colloid under physiological conditions. Moreover, such colloids can be modified by electrochemical polymerization resulting, e.g. in conductive polymer-coated spheres, which in addition may be loaded with specific dopants. In contrast to other AFM-based single cell force spectroscopy measurements, these probes allow adhesion measurements at the cell-biomaterial interface on multiple cells in a rapid manner while the properties of the polymer can be changed by applying a bias. In addition, spatially resolved electrochemical information e.g., oxygen reduction can be obtained simultaneously. Conductive colloid AFM-SECM probes modified with poly(3,4-ethylenedioxythiophene) doped with polystyrene sulfonate (PEDOT:PSS) are used for single cell force measurements in mouse fibroblasts and single cell interactions are investigated as a function of the applied potential.Conductive colloidal probe Atomic Force-Scanning Electrochemical Microscopy (AFM-SECM) is a new approach, which employs electrically insulated AFM probes except for a gold-coated colloid located at the end of the cantilever. Hence, force measurements can be performed while biasing the conductive colloid under physiological conditions. Moreover, such colloids can be modified by electrochemical polymerization resulting, e.g. in conductive polymer-coated spheres, which in addition may be loaded with specific dopants. In contrast to other AFM-based single cell force spectroscopy measurements, these probes allow adhesion measurements at the cell-biomaterial interface on multiple cells in a rapid manner while the properties of the polymer can be changed by applying a bias. In addition, spatially resolved electrochemical

  4. Surface adsorption of sulfonated poly(phenylene sulfone)/C14TAB mixtures and its correlation with foam film stability.

    PubMed

    Uhlig, Martin; Miller, Reinhard; Klitzing, Regine von

    2016-07-21

    Polyelectrolyte/surfactant mixtures of rigid monosulfonated poly(phenylene sulfone) (sPSO2-220) and tetradecyl trimethylammonium bromide (C14TAB) were investigated by surface tension, surface elasticity and foam film stability measurements. The results were compared to former measurements of polyelectrolyte/surfactant mixtures containing more flexible polyelectrolytes (PAMPS or PSS and C14TAB). For all polyelectrolyte/surfactant mixtures an increased surface adsorption in comparison to the pure surfactant was detected. Moreover, sPSO2-220/C14TAB mixtures showed a much higher surface activity and foam film stability than mixtures with more flexible polyelectrolytes. The results presented give insight into the surface adsorption and foam film formation of rigid polyelectrolyte/surfactant mixtures. Therefore, this study helps to understand the role of polyelectrolyte backbone rigidity in the formation and stabilization of foam films made from polyelectrolyte/surfactant mixtures.

  5. Excimer laser patterning of PEDOT:PSS thin-films on flexible barrier foils: A surface analysis study

    NASA Astrophysics Data System (ADS)

    Naithani, Sanjeev; Schaubroeck, David; Vercammen, Yannick; Mandamparambil, Rajesh; Yakimets, Iryna; Van Vaeck, Luc; Van Steenberge, Geert

    2013-09-01

    Selective laser patterning of thin organic films is an important aspect in the roll-to-roll production of organic electronic devices such as organic light emitting diodes (OLEDs). An excimer laser is well suited for the patterning and structuring of polymer thin films as their UV absorption is significant. Selective removal of a transparent conducting polymer PEDOT:PSS (poly(3,4-ethylene dioxythiophene):polystyrene sulfonate) on a multilayered (inorganic-organic-inorganic) barrier and a flexible PEN (polyethylene napthalate) substrate has been studied using a KrF excimer laser. The ablation craters were characterized with electron microscopy and profilometry. For the first time, chemical surface analysis of the patterned area was performed with Time-Of-Flight Static Secondary Ion Mass Spectrometry (TOF-S-SIMS), providing a detailed insight of the surface composition after laser ablation and plasma post-treatments.

  6. PSS-SQL: protein secondary structure - structured query language.

    PubMed

    Mrozek, Dariusz; Wieczorek, Dominika; Malysiak-Mrozek, Bozena; Kozielski, Stanislaw

    2010-01-01

    Secondary structure representation of proteins provides important information regarding protein general construction and shape. This representation is often used in protein similarity searching. Since existing commercial database management systems do not offer integrated exploration methods for biological data e.g. at the level of the SQL language, the structural similarity searching is usually performed by external tools. In the paper, we present our newly developed PSS-SQL language, which allows searching a database in order to identify proteins having secondary structure similar to the structure specified by the user in a PSS-SQL query. Therefore, we provide a simple and declarative language for protein structure similarity searching.

  7. Potential of Wood-Rotting Fungi to Attack Polystyrene Sulfonate and Its Depolymerisation by Gloeophyllum trabeum via Hydroquinone-Driven Fenton Chemistry.

    PubMed

    Krueger, Martin C; Hofmann, Ulrike; Moeder, Monika; Schlosser, Dietmar

    2015-01-01

    Synthetic polymers often pose environmental hazards due to low biodegradation rates and resulting accumulation. In this study, a selection of wood-rotting fungi representing different lignocellulose decay types was screened for oxidative biodegradation of the polymer polystyrene sulfonate (PSS). Brown-rot basidiomycetes showed PSS depolymerisation of up to 50 % reduction in number-average molecular mass (Mn) within 20 days. In-depth investigations with the most efficient depolymeriser, a Gloeophyllum trabeum strain, pointed at extracellular hydroquinone-driven Fenton chemistry responsible for depolymerisation. Detection of hydroxyl radicals present in the culture supernatants showed good compliance with depolymerisation over the time course of PSS degradation. 2,5-Dimethoxy-1,4-hydroquinone (2,5-DMHQ), which was detected in supernatants of active cultures via liquid chromatography and mass spectrometry, was demonstrated to drive the Fenton processes in G. trabeum cultures. Up to 80% reduction in Mn of PSS where observed when fungal cultures were additionally supplemented with 2,5-dimethoxy benzoquinone, the oxidized from of 2,5-DMHQ. Furthermore, 2,5-DMHQ could initiate the Fenton's reagent-mediated PSS depolymerisation in cell-free systems. In contrast, white-rot fungi were unable to cause substantial depolymerising effects despite the expression of lignin-modifying exo-enzymes. Detailed investigations with laccase from Trametes versicolor revealed that only in presence of certain redox mediators limited PSS depolymerisation occurred. Our results indicate that brown-rot fungi might be suitable organisms for the biodegradation of recalcitrant synthetic polymeric pollutants.

  8. 21 CFR 573.600 - Lignin sulfonates.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Lignin sulfonates. 573.600 Section 573.600 Food... Additive Listing § 573.600 Lignin sulfonates. Lignin sulfonates may be safely used in animal feeds in... feeds, as liquid lignin sulfonate, in an amount not to exceed 11 percent of the molasses. (4) As...

  9. 21 CFR 573.600 - Lignin sulfonates.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Lignin sulfonates. 573.600 Section 573.600 Food... Additive Listing § 573.600 Lignin sulfonates. Lignin sulfonates may be safely used in animal feeds in... feeds, as liquid lignin sulfonate, in an amount not to exceed 11 percent of the molasses. (4) As...

  10. A novel composite material of graphene and PEDOT:PSS

    NASA Astrophysics Data System (ADS)

    Pathak, C. S.; Singh, J. P.; Singh, R.

    2016-05-01

    A novel composite material has been prepared by using graphene and Poly (3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS). It shows excellent electrical conductivity and transparency in visible region. The conductivity is enhanced and the films are highly transparent more than 80% in entire visible region. The highly transparent composite material can be used in optoelectronic devices.

  11. Adsorption of polystyrene sulfonate to the air surface of water by neutron reflectivity

    SciTech Connect

    YIM,HYUN; KENT,MICHAEL S.; MATHESON,AARON J.; IVKOV,R.; SATIJA,S.; MAJEWSKI,J.; SMITH,G.S.

    2000-05-16

    The adsorption of the strong polyelectrolyte polystyrene sulfonate (PSS) to the air surface of dilute aqueous solutions was investigated as a function of molecular weight and salt concentration. Detailed segment profiles of the deuterated polymer were determined by neutron reflection. Surface activity was also examined through surface tension measurements. In general, the segment profiles are composed of a thin layer (10--20 {angstrom} thick) of high concentration at the air surface, followed by a distinct second layer of much lower segment concentration that extends to larger depths into the liquid. The high segment density at the air surface is due to a strong surface attraction, arising from the low surface tension of the PSS backbone relative to the surface tension of water. At low salt concentration, the profiles tend toward a single dense layer, suggesting that the chains lie nearly flat at the interface in that limit. The adsorbed amount increases with salt concentration, with a stronger dependence for higher molecular weight chains. The adsorbed amounts at the air/water interface are higher than reported previously for PSS adsorbed onto neutral solid surfaces, consistent with the fact that the air-liquid interface provides a stronger surface attraction. While the trends of adsorbed amount and layer thickness with salt concentration and molecular weight are in good agreement with numerical self-consistent field lattice calculations, the measured bilayer profiles are rather different from the smoothly decaying theoretical profiles. The surface tensions of the PSS solutions are significantly lowered relative to those of pure salt solutions. Combining the reflectivity and surface tension measurements, an approximately linear relationship is established between the surface pressure and the PSS adsorbed amount.

  12. Solution-processed highly conductive PEDOT:PSS/AgNW/GO transparent film for efficient organic-Si hybrid solar cells.

    PubMed

    Xu, Qiaojing; Song, Tao; Cui, Wei; Liu, Yuqiang; Xu, Weidong; Lee, Shuit-Tong; Sun, Baoquan

    2015-02-11

    Hybrid solar cells based on n-Si/poly(3,4-ethylenedioxythiophene):poly(styrene- sulfonate) (PEDOT:PSS) heterojunction promise to be a low cost photovoltaic technology by using simple device structure and easy fabrication process. However, due to the low conductivity of PEDOT:PSS, a metal grid deposited by vacuum evaporation method is still required to enhance the charge collection efficiency, which complicates the device fabrication process. Here, a solution-processed graphene oxide (GO)-welded silver nanowires (AgNWs) transparent conductive electrode (TCE) was employed to replace the vacuum deposited metal grid. A unique "sandwich" structure was developed by embedding an AgNW network between PEDOT:PSS and GO with a figure-of-merit of 8.6×10(-3) Ω(-1), which was even higher than that of sputtered indium tin oxide electrode (6.6×10(-3) Ω(-1)). A champion power conversion efficiency of 13.3% was achieved, because of the decreased series resistance of the TCEs as well as the enhanced built-in potential (Vbi) in the hybrid solar cells. The TCEs were obtained by facile low-temperature solution process method, which was compatible with cost-effective mass production technology. PMID:25599588

  13. Pseudo-spark switch (PSS) characteristics under different operation conditions

    NASA Astrophysics Data System (ADS)

    Hamad, B. H.; Lateef, K. H.; Ahmad, A. K.

    2016-08-01

    The present paper concentrates on the characteristics of the pseudospark switch (PSS) designed in a previous work. The special characteristics of PSS make it a replacement for other high voltage switches such as thyratrons and ordinary high-pressure spark gaps. PSS is characterized by short rise time and small jitter time. The pseudo park chamber consists of two hollow cylindrical electrodes made of a stainless steel material (type 306L) separated by an insulator. The insulator used in our design is a glazed ceramic 70 mm in diameter and 3.5 mm in thickness. A PSS with an anode voltage of 29.2 kV, and a current of 3.6 kA and 11 ns rise time was achieved and used successfully at a repetition rate of about 2.2 kHz. A simple trigger circuit designed, built, and used effectively reaching more than 1.56 kV trigger pulse which is sufficient to ignite the argon gas inside the cathode to cause a breakdown. A non-inductive dummy load is designed to be a new technique to find the accurate value of the PSS inductance. A jitter time of ±10 ns pulses is observed to occur in a reliable manner for more than 6 h of continuous operation. In this research, the important parameters of this switch like rise time, peak current, and anode voltage were studied at various values of charging capacitance. The lifetime of this system is depending on the kind of the electrode material and on the type of insulation material in the main gap of the pseudospark switch.

  14. Correlation between near infrared-visible absorption, intrinsic local and global sheet resistance of poly(3,4-ethylenedioxy-thiophene) poly(styrene sulfonate) thin films

    NASA Astrophysics Data System (ADS)

    Herrmann, Felix; Engmann, Sebastian; Presselt, Martin; Hoppe, Harald; Shokhovets, Sviatoslav; Gobsch, Gerhard

    2012-04-01

    The ordinary dielectric function of poly(3,4-ethylenedioxy-thiophene) poly(styrene sulfonate) (PEDOT:PSS) thin films was measured using a combination of spectroscopic ellipsometry and photothermal deflection spectroscopy. This method combination allows for a highly sensitive optical characterization of thin films. Hence, even the detection of weak sub-bandgap and intra-band absorptions is enabled. These intraband transitions of free charge carriers were modeled using a Drude-type oscillator to derive an intrinsic resistances for PEDOT:PSS. These optically derived resistances were compared with those determined by a 4-probe measurement setup for two different types of PEDOT:PSS and for varied annealing temperatures. Good agreement between optical and electrical measurements could be obtained for annealing temperatures smaller than 180∘C. Therefore, we conclude that the proposed combination of our two optical methods is well suited to determine electrical resistances of organic layers.

  15. Comparison of properties of polymer organic solar cells prepared using highly conductive modified PEDOT:PSS films by spin- and spray-coating methods

    NASA Astrophysics Data System (ADS)

    Kumar, Palanisamy; Santhakumar, Kannappan; Tatsugi, Jiro; Shin, Paik-Kyun; Ochiai, Shizuyasu

    2014-01-01

    Bulk heterojunction (BHJ) solar cells have made great progress over the past decade and consequently are now attracting extensive academic and commercial interest because of their potential advantages: lightweight, flexible, low cost, and high-throughput production. Polymer conductivity is a key factor for improving the performance of electronic and photonic devices. Poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) is promising for use as a next-generation transparent electrode of optoelectronic devices. In this research, we compare the effect of nanomorphology on conductivity, and power conversion efficiency of polymer organic solar cells prepared by the spin- and spray-coating methods. To improve the conductivity of spray-deposited PEDOT:PSS, we modified the PEDOT:PSS films by simple UV irradiation and by UV irradiation with treatment using various solvents such as methanol, ethanol, acetone, acetonitrile, hydrochloric acid, and sulfuric acid to form a hole transport layer (HTL). The active layer of PTB7:PC70BM is spray-coated on top of the PEDOT:PSS layer. The films were examined by optical spectroscopy, micro-Raman spectroscopy, and conductivity measurements. The surface morphology of the deposited films was examined by atomic force microscopy (AFM). The current density-voltage (J-V) characteristics were measured under illumination with simulated solar light at 100 mW/cm2 (AM 1.5G) using an oriel 1000 W solar simulator. The obtained results are expected to have a considerable impact and suggest a bright future for organic polymer solar cells.

  16. Thermal stability of sulfonated polymers

    SciTech Connect

    Audibert, A.; Argillier, J.F.

    1995-11-01

    Polyacrylamides which are used in oil applications i.e. polymer flooding and water based muds, are hydrolyzed versus time and temperature. This leads to a lack of tolerance towards electrolyte contamination and to a rapid degradation inducing a loss of their properties. Modifications of polyacrylamide structure have been proposed to postpone their thermal stability to higher temperatures. Monomers such as acrylamido methylpropane sulfonate (AMPS) or sulfonated styrene/maleic anhydride can be used to prevent acrylamide comonomer from hydrolysis. The aim of this work is to study under controlled conditions, i.e. anaerobic atmosphere, neutral pH, the stability of sulfonated polymers in order to distinguish between hydrolysis and radical degradation reactions. It has been observed that up to 100 C, the AMPS group is stable and protects the acrylamide function from hydrolysis up to 80%. At higher temperature, even the hydrolysis of the AMPS group occurs, giving acrylate and {beta},{beta} dimethyl taurine, with a kinetics that depends on temperature and time. Degradation in terms of molecular weight then occurs indicating that it follows a radical decarboxylation reaction. It can be limited either by the use of free radical scavenger or when the polymer is in the presence of a mineral phase such as bentonite. These results provide valuable data for the determination of the limits of use of sulfonated copolymers and guidelines for optimizing chemical structure of sulfonated polymers used in water based formulation, in particular to enhance their thermal stability.

  17. Profiling sulfonate ester stability: identification of complementary protecting groups for sulfonates

    PubMed Central

    Miller, Stephen C.

    2010-01-01

    Sulfonation is prized for its ability to impart water-solubility to hydrophobic molecules such as dyes. This modification is usually performed as a final step, since sulfonated molecules are poorly soluble in most organic solvents, which complicates their synthesis and purification. This work compares the intrinsic lability of different sulfonate esters, identifying new sulfonate protecting groups and mild, selective cleavage conditions. PMID:20515067

  18. Electrically conductive poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate)/polyacrylonitrile fabrics for humidity sensors

    NASA Astrophysics Data System (ADS)

    Panapoy, Manop; Singsang, Witawat; Ksapabutr, Bussarin

    2010-05-01

    Humidity sensors based on poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate) (PEDOT-PSS)/polyacrylonitrile (PAN) nanofiber fabric were fabricated by a dip coating of nonwoven PAN nanofiber mat, which was prepared via an electrospinning method, in PEDOT-PSS solution. The influence of PAN solution concentration on their responsiveness to humidity on dynamic testing was monitored as the device was exposed to humidity. With the relative humidity (RH) changing from 0 to 100%, a resistance device response over 110% was achieved, and the curve of the resistance response with RH is of high linearity at the humidity working range of 0-100% RH. The high device reproducibility was demonstrated by carrying out vapor adsorption-desorption dynamic cycles, and the response and recovery times were determined to be of the order of 2-46 and 7-34 s, respectively. These hybrid polymer sensors can be used as disposable handheld instruments due to low cost and light weight.

  19. Sulfone cosurfactants in enhanced oil recovery processes

    SciTech Connect

    Stapp, P. R.

    1984-12-04

    A surfactant system useful for oil recovery consisting essentially of a NaCl, a hydrocarbon sulfonate surfactant, such as a petroleum sulfonate, and a cosurfactant such as a sulfone or sulfolane derivative. In another embodiment, a C/sub 1/ to C/sub 8/ alcohol is additionally present as a cosurfactant.

  20. Safety assessment of xylene sulfonic acid, toluene sulfonic acid, and alkyl aryl sulfonate hydrotropes as used in cosmetics.

    PubMed

    Bergfeld, Wilma F; Belsito, Donald V; Klaassen, Curtis D; Hill, Ronald; Liebler, Daniel; Marks, James G; Shank, Ronald C; Slaga, Thomas J; Snyder, Paul W; Andersen, F Alan

    2011-12-01

    Xylene sulfonic acid, toluene sulfonic acid, and alkyl aryl sulfonate hydrotropes used in cosmetics as surfactants, hydrotropes, were reviewed in this safety assessment. The similar structure, properties, functions, and uses of these ingredients enabled grouping them and using the available toxicological data to assess the safety of the entire group. The Cosmetic Ingredient Review Expert Panel reviewed relevant animal and human data related to these ingredients. The panel concluded that xylene sulfonic acid and alkyl aryl sulfonate hydrotropes are safe as cosmetic ingredients in the present practices of use and concentrations as described in this safety assessment, when formulated to be nonirritating.

  1. Influence of salt and rinsing protocol on the structure of PAH/PSS polyelectrolyte multilayers.

    PubMed

    Feldötö, Zsombor; Varga, Imre; Blomberg, Eva

    2010-11-16

    A quartz crystal microbalance (QCM) and dual polarization interferometry (DPI) have been utilized to study how the structure of poly(allylamine hydrochloride) (PAH)/poly(styrene sulfonate) (PSS) multilayers is affected by the rinsing method (i.e., the termination of polyelectrolyte adsorption). The effect of the type of counterions used in the deposition solution was also investigated, and the polyelectrolyte multilayers were formed in a 0.5 M electrolyte solution (NaCl and KBr). From the measurements, it was observed that thicker layers were obtained when using KBr in the deposition solution than when using NaCl. Three different rinsing protocols have been studied: (i) the same electrolyte solution as used during multilayer formation, (ii) pure water, and (iii) first a salt solution (0.5 M) and then pure water. When the multilayer with PAH as the outermost layer was exposed to pure water, an interesting phenomenon was discovered: a large change in the energy dissipation was measured with the QCM. This could be attributed to the swelling of the layer, and from both QCM and DPI it is obvious that only the outermost PAH layer swells (to a thickness of 25-30 nm) because of a decrease in ionic strength and hence an increase in intra- and interchain repulsion, whereas the underlying layers retain a very rigid and compact structure with a low water content. Interestingly, the outermost PAH layer seems to obtain very similar thicknesses in water independent of the electrolyte used for the multilayer buildup. Another interesting aspect was that the measured thickness with the DPI evaluated by a single-layer model did not correlate with the estimated thickness from the model calculations performed on the QCM-D data. Thus, we applied a two-layer model to evaluate the DPI data and the results were in excellent agreement with the QCM-D results. To our knowledge, this evaluation of DPI data has not been done previously.

  2. p-Chlorophenyl methyl sulfone

    Integrated Risk Information System (IRIS)

    p - Chlorophenyl methyl sulfone ; CASRN 98 - 57 - 7 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for No

  3. Phycotoxicity of linear alkylbenzene sulfonate

    SciTech Connect

    Chawla, G.; Viswanathan, P.N.; Devi, S.

    1988-04-01

    Dose- and time-dependent effects of linear alkylbenzene sulfonate, a major component of synthetic detergent, to the blue-green alga Nostoc muscorum, were studied under laboratory conditions. Toxicity was evident, at doses above 0.001%, from the decrease in biomass, heterocyst number, and protein content and pathomorphological alterations.

  4. Process for sulfonation of gas oils

    SciTech Connect

    Berg, R. C.

    1980-12-23

    A process for the production of oil-soluble sulfonates from a gas oil such as a vacuum gas oil. Water-soluble sulfonic acids are separated from the effluent of the sulfonation zone, and the remainder of the effluent is then passed through a saponification zone to produce oil-soluble sulfonates which are then recovered. The remaining hydrocarbons are fractionated, with the resultant heavy fraction being passed through a reforming zone to produce additional aromatics which are then recycled to the sulfonation zone.

  5. Effect of alcohol vapor treatment on electrical and optical properties of poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate) films for indium tin oxide-free organic light-emitting diodes

    NASA Astrophysics Data System (ADS)

    Fallahzadeh, Ali; Saghaei, Jaber; Yousefi, Mohammad Hassan

    2014-11-01

    A simple alcohol vapor treatment (AVT) technique was proposed to improve the conductivity of poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) films. In this technique, various alcohols, i.e. methanol, ethanol, 2-propanol and ethylene glycol, were applied to treat the surface of the films formed and then they were annealed. The sheet resistance of PEDOT:PSS films was significantly reduced from 130 kΩ/sq to 60 Ω/sq when treated with methanol vapor. The investigation of the vertical resistance of the films showed that the sample treated with methanol vapor displayed the lowest resistance as well. The mechanism of conductivity enhancement of PEDOT:PSS films through AVT method was explained by surface phase images, UV and IR spectra of PEDOT:PSS films. Optical transmittance spectrum of treated films exhibited that AVT has even enhanced the optical transmittance slightly. Improvement in the morphology, electrical and optical properties of PEDOT:PSS films prompted their applications as a transparent anode in the fabrication of ITO-free organic light-emitting diodes (OLEDs). The OLED manufactured based on methanol-treated PEDOT:PSS films demonstrated the highest luminance.

  6. Transparent and conductive PEDOT:PSS/Ag NW/PEDOT:PSS hybrid films prepared by spin-coating at room temperature

    NASA Astrophysics Data System (ADS)

    Qingqing, Yue; Jinliang, Yan; Delan, Meng

    2015-12-01

    PEDOT:PSS/Ag NW/PEDOT:PSS hybrid films were deposited on PET substrates by the spin coating technique at room temperature. The optical transmittance, sheet resistance, crystallization and surface morphology were characterized by using the double beam spectrophotometer, Hall effect system, X-ray diffractometer and field emission scanning electron microscopy. XRD patterns of the hybrid films display characteristic diffraction peaks of Ag (111) and Ag (200), and the Ag NW networks have a polycrystalline structure with a Ag (111) preferred orientation. A high transmittance of 83.95% at the 550 nm wavelength and a low sheet resistance of 21.98 Ω/□ are achieved for 3-PEDOT:PSS/5-Ag NW/3-PEDOT:PSS hybrid films. Project supported by the National Natural Science Foundation of China (No. 10974077), and the Innovation Project of Shandong Graduate Education, China (No. SDYY13093).

  7. Copolymers of fluorinated polydienes and sulfonated polystyrene

    DOEpatents

    Mays, Jimmy W.; Gido, Samuel P.; Huang, Tianzi; Hong, Kunlun

    2009-11-17

    Copolymers of fluorinated polydienes and sulfonated polystyrene and their use in fuel cell membranes, batteries, breathable chemical-biological protective materials, and templates for sol-gel polymerization.

  8. Potential of Wood-Rotting Fungi to Attack Polystyrene Sulfonate and Its Depolymerisation by Gloeophyllum trabeum via Hydroquinone-Driven Fenton Chemistry

    PubMed Central

    Krueger, Martin C.; Hofmann, Ulrike; Moeder, Monika; Schlosser, Dietmar

    2015-01-01

    Synthetic polymers often pose environmental hazards due to low biodegradation rates and resulting accumulation. In this study, a selection of wood-rotting fungi representing different lignocellulose decay types was screened for oxidative biodegradation of the polymer polystyrene sulfonate (PSS). Brown-rot basidiomycetes showed PSS depolymerisation of up to 50 % reduction in number-average molecular mass (Mn) within 20 days. In-depth investigations with the most efficient depolymeriser, a Gloeophyllum trabeum strain, pointed at extracellular hydroquinone-driven Fenton chemistry responsible for depolymerisation. Detection of hydroxyl radicals present in the culture supernatants showed good compliance with depolymerisation over the time course of PSS degradation. 2,5-Dimethoxy-1,4-hydroquinone (2,5-DMHQ), which was detected in supernatants of active cultures via liquid chromatography and mass spectrometry, was demonstrated to drive the Fenton processes in G. trabeum cultures. Up to 80% reduction in Mn of PSS where observed when fungal cultures were additionally supplemented with 2,5-dimethoxy benzoquinone, the oxidized from of 2,5-DMHQ. Furthermore, 2,5-DMHQ could initiate the Fenton's reagent-mediated PSS depolymerisation in cell-free systems. In contrast, white-rot fungi were unable to cause substantial depolymerising effects despite the expression of lignin-modifying exo-enzymes. Detailed investigations with laccase from Trametes versicolor revealed that only in presence of certain redox mediators limited PSS depolymerisation occurred. Our results indicate that brown-rot fungi might be suitable organisms for the biodegradation of recalcitrant synthetic polymeric pollutants. PMID:26147966

  9. Conductivity of PEDOT:PSS on Spin-Coated and Drop Cast Nanofibrillar Cellulose Thin Films

    NASA Astrophysics Data System (ADS)

    Valtakari, Dimitar; Liu, Jun; Kumar, Vinay; Xu, Chunlin; Toivakka, Martti; Saarinen, Jarkko J.

    2015-10-01

    Aqueous dispersion of conductive polymer poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) was deposited on spin-coated and drop cast nanofibrillar cellulose (NFC)-glycerol (G) matrix on a glass substrate. A thin glycerol film was utilized on plasma-treated glass substrate to provide adequate adhesion for the NFC-glycerol (NFC-G) film. The effects of annealing temperature, the coating method of NFC-G, and the coating time intervals on the electrical performance of the PEDOT:PSS were characterized. PEDOT:PSS on drop cast NFC-G resulted in 3 orders of magnitude increase in the electrical conductivity compared to reference PEDOT:PSS film on a reference glass substrate, whereas the optical transmission was only slightly decreased. The results point out the importance of the interaction between the PEDOT:PSS and the NFC-G for the electrical and barrier properties for thin film electronics applications.

  10. Development and calibration of a 3-PSS parallel CMM

    NASA Astrophysics Data System (ADS)

    Wang, Jing; Hu, Penghao; Li, Songyuan; Bao, Xinxin

    2013-01-01

    A new 3-DOF parallel Coordinate Measuring Machine was proposed in this paper, which could realize 3D measured with only one linear grating and one precision guide. A kind of calibration method based on the distance of two points is proposed. In the scheme gauge block is utilized as benchmark, Gauss-Newton method, a non-linear least square computational method, is used to solve the measuring equation of the CMM, to get the precise parameter of the machine. Experimental results show that this method can effectively improve the over-all accuracy of the 3-PSS CMM. The further study is in process, we will identify the actual values of input parameter errors and mechanical errors in the software compensation.

  11. Model Calibration of Exciter and PSS Using Extended Kalman Filter

    SciTech Connect

    Kalsi, Karanjit; Du, Pengwei; Huang, Zhenyu

    2012-07-26

    Power system modeling and controls continue to become more complex with the advent of smart grid technologies and large-scale deployment of renewable energy resources. As demonstrated in recent studies, inaccurate system models could lead to large-scale blackouts, thereby motivating the need for model calibration. Current methods of model calibration rely on manual tuning based on engineering experience, are time consuming and could yield inaccurate parameter estimates. In this paper, the Extended Kalman Filter (EKF) is used as a tool to calibrate exciter and Power System Stabilizer (PSS) models of a particular type of machine in the Western Electricity Coordinating Council (WECC). The EKF-based parameter estimation is a recursive prediction-correction process which uses the mismatch between simulation and measurement to adjust the model parameters at every time step. Numerical simulations using actual field test data demonstrate the effectiveness of the proposed approach in calibrating the parameters.

  12. Role of electroless nickel diffusion barrier on the combinatorial plating characteristics of dense Pd/Ni/PSS composite membranes

    NASA Astrophysics Data System (ADS)

    Pujari, Murali; Agarwal, Amrita; Uppaluri, Ramgopal; Verma, Anil

    2014-06-01

    This work addresses the combinatorial plating characteristics of dense Pd/Ni/porous stainless steel (PSS) composite membranes in comparison with Pd/PSS membranes. While Pd/PSS membranes were fabricated using 0.1 μm nominal pore size PSS supports, Pd/Ni/PSS membranes were fabricated using 0.5 and 0.1 μm nominal pore size PSS supports. Both Ni and Pd films were deposited using an identified novel electroless plating process that characterizes the optimal utilization of surfactant, sonication and reducing agent contacting pattern in Pd electroless plating baths. It was observed that the combinatorial plating characteristics for Pd/Ni/PSS membranes were significantly different and poorer in comparison with those obtained for the Pd/PSS membranes. In summary, it has been inferred that the introduction of nickel interdiffusion barrier was not fruitful to reduce the critical thickness of dense Pd film without jeopardizing upon the pore densification.

  13. Sulfonated poly(arylene ether sulfone)s with phosphine oxide moieties: a promising material for proton exchange membranes.

    PubMed

    Fu, Lingchao; Xiao, Guyu; Yan, Deyue

    2010-06-01

    Sulfonated poly(arylene ether sulfone)s with phosphine oxide moieties (sPESPO) were achieved by polycondensation of bis(4-hydroxyphenyl)phenylphosphine oxide with 3,3'-disulfonate-4,4'-difluorodiphenyl sulfone (SFDPS) and 4-fluorophenyl sulfone (FPSF). Sulfonated poly(arylene ether sulfone)s (sPES) were also synthesized by polymerization of 4,4'-sulfonyldiphenol with SFDPS and FPSF for comparison. The comparative study demonstrates that the sPESPO ionomers exhibit strong intermolecular interactions and high oxidative stability because of the phosphine oxide groups. Furthermore, the sPESPO membrane and the sPES membrane with an equal ion exchange capacity show much different nanophase separation morphology. As a result, the former shows better properties than the latter. The sPESPO membranes exhibit excellent overall properties. For instance, the sPESPO membrane, with a disulfonation degree of 45%, exhibits high thermal and oxidative stability. Moreover, it shows a water uptake of 30.8% and a swelling ratio of 15.8% as well as a proton conductivity of 0.087 S/cm at 80 degrees C.

  14. Transport behavior of hairless mouse skin during constant current DC iontophoresis, part 2: iontophoresis of nonionic molecules with cotransport of polystyrene sulfonate oligomers.

    PubMed

    Liddell, Mark R; Li, S Kevin; Higuchi, William I

    2011-07-01

    The purpose of this study was to characterize changes that occur in the iontophoretic transport of nonionic probe permeants in hairless mouse skin epidermal membrane from the anode to cathode when polystyrene sulfonate (PSS) oligomers are cotransported from the cathode to anode. The experiments were conducted with trace levels of the nonionic probe permeants: urea, mannitol, and raffinose. In order to systematically assess changes that occur as a result of having PSS in the cathodal chamber, the steady-state transport parameters of the membrane and the experimental permeability coefficients of the probe permeants were determined and compared with results obtained from earlier baseline experiments where both the cathodal and anodal chamber media were phosphate buffered saline. In addition, the physicochemical properties of the PSS solutions were determined including the solution viscosity and conductance as well as the mobilities of individual PSS oligomers. The effective pore radii of the transport pathways were calculated using a theoretical expression based on simultaneous diffusion and electroosmosis. Compared with the baseline results, the calculated radii were found to have increased up to around twofold and the iontophoretic fluxes of the probe permeants increased by as much sixfold.

  15. Oil recovery method utilizing an alkylarylpoxyalkylene sulfonate

    SciTech Connect

    McCoy, D.R.

    1984-08-14

    An alkylarylpolyalkoxyalkylene sulfonate alone or combined with a water soluble petroleum sulfonate surfactant is dissolved in water to form an effective surfactant fluid that is stable in high salinity environments. The surfactant fluid is injected into an underground petroleum-containing reservoir in an enhanced oil recovery process.

  16. Influence of solvent treatment with fluoro compounds on the properties of poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) polymer as a hole transport layer in polymer solar cells

    NASA Astrophysics Data System (ADS)

    Kumar, Palanisamy; Kumar, Abhirami; Shin, Paik-Kyun; Ochiai, Shizuyasu

    2014-01-01

    We prepared high conducting poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) by solvent additives for using as a hole transport layer (HTL) in polymer solar cells (PSCs). PEDOT:PSS films treated with fluoro compounds of hexafluoroacetone (HFA) and hexafluoroisoproponal (HFIPA) with various concentrations show a significant enhancement in electrical conductivity without compromising optical transparency. The conductivity increased from 0.2 to 1053 and 746 S/cm after 4 vol. % HFA and 6 vol. % HFIPA treatments, respectively. The high performance of the PEDOT:PSS layer is attributed to preferential phase segregation of PEDOT:PSS with HFA and HFIPA solvent mixture treatment methods. The improved performance of PSC was dependent on the structure of organic solvents and the concentration of fluoro compounds in PEDOT:PSS solution. Using these optimized layers, conjugated PSCs with a poly[[9-(1-octylnonyl)-9H-carbazole-2,7-diyl]-2,5-thiophenediyl-2,1,3-benzothiadiazole-4,7-diyl-2,5 thiophenediyl] polymer:[6,6]-phenyl-C71-butyric acid methyl esters (PCDTBT:PC71BM) bulk heterojunction have been produced. The high power conversion efficiency (PCE) of 4.10% and 3.98% were observed for PEDOT:PSS films treated with 4 vol. % HFA and 6 vol. % HFIPA treatments, respectively. The obtained results show that PEDOT:PSS optimized with HFA and HFIPA organic solvents can be a very promising candidate for transparent anode buffer layer in the low cost organic solar cell devices.

  17. Psychometric properties of a European Spanish version of the Perceived Stress Scale (PSS).

    PubMed

    Remor, Eduardo

    2006-05-01

    This paper presents evidence from a heterogeneous sample of 440 Spanish adults, for the reliability and validity of a European Spanish version of the Perceived Stress Scale (PSS), designed to measure the degree to which situations in one's life are appraised as stressful. The European Spanish version PSS (14-item) demonstrated adequate reliability (internal consistency, alpha = .81, and test-retest, r = .73), validity (concurrent), and sensitivity. Additional data indicate adequate reliability (alpha = .82, test-retest, r = .77), validity, and sensitivity of a 10-item short version of the PSS. PMID:16673626

  18. Correlating electronic structure and chemical durability of sulfonated poly(arylene ether sulfone)s

    NASA Astrophysics Data System (ADS)

    Lawrence, Jimmy; Yamashita, Koichi; Yamaguchi, Takeo

    2015-04-01

    Many different proton-conducting polymeric materials have been developed for polymer electrolyte membrane fuel cells (PEMFCs). The development of perfluorosulfonic acid-based, polymer electrolyte membranes (PFSA-PEMs) was followed by aromatic hydrocarbon-based PEMs (HC-PEMs), which allow for tailored design and optimization of their molecular structures. Although many new PFSA-PEMs and HC-PEMs have shown promising proton conductivity and thermal stability, chemical degradation of these materials in an oxidizing environment remains a significant technical barrier in PEMFC development. Here, we used accelerated degradation tests and electronic structure analysis to examine the chemical stability of sulfonated poly(arylene ether sulfone) (SPES) copolymers, a highly thermally stable HC-PEM. HOMO levels, the presence of main chain-protecting steric groups, and HOMO-LUMO location along the main chain have significant effects on the chain scission modes and degradation rate of SPES copolymers. Rational design of HC-PEMs to suppress midpoint scission can open many opportunities in the development of highly robust polymer electrolytes for fuel cell and other energy storage applications.

  19. PEDOT:PSS as multi-functional composite material for enhanced Li-air-battery air electrodes

    PubMed Central

    Yoon, Dae Ho; Yoon, Seon Hye; Ryu, Kwang-Sun; Park, Yong Joon

    2016-01-01

    We propose PEDOT:PSS as a multi-functional composite material for an enhanced Li-air-battery air electrode. The PEDOT:PSS layer was coated on the surface of carbon (graphene) using simple method. A electrode containing PEDOT:PSS-coated graphene (PEDOT electrode) could be prepared without binder (such as PVDF) because of high adhesion of PEDOT:PSS. PEDOT electrode presented considerable discharge and charge capacity at all current densities. These results shows that PEDOT:PSS acts as a redox reaction matrix and conducting binder in the air electrode. Moreover, after cycling, the accumulation of reaction products due to side reaction in the electrode was significantly reduced through the use of PEDOT:PSS. This implies that PEDOT:PSS coating layer can suppress the undesirable side reactions between the carbon and electrolyte (and/or Li2O2), which causes enhanced Li-air cell cyclic performance. PMID:26813852

  20. PEDOT:PSS as multi-functional composite material for enhanced Li-air-battery air electrodes

    NASA Astrophysics Data System (ADS)

    Yoon, Dae Ho; Yoon, Seon Hye; Ryu, Kwang-Sun; Park, Yong Joon

    2016-01-01

    We propose PEDOT:PSS as a multi-functional composite material for an enhanced Li-air-battery air electrode. The PEDOT:PSS layer was coated on the surface of carbon (graphene) using simple method. A electrode containing PEDOT:PSS-coated graphene (PEDOT electrode) could be prepared without binder (such as PVDF) because of high adhesion of PEDOT:PSS. PEDOT electrode presented considerable discharge and charge capacity at all current densities. These results shows that PEDOT:PSS acts as a redox reaction matrix and conducting binder in the air electrode. Moreover, after cycling, the accumulation of reaction products due to side reaction in the electrode was significantly reduced through the use of PEDOT:PSS. This implies that PEDOT:PSS coating layer can suppress the undesirable side reactions between the carbon and electrolyte (and/or Li2O2), which causes enhanced Li-air cell cyclic performance.

  1. Charge injection and accumulation in organic light-emitting diode with PEDOT:PSS anode

    SciTech Connect

    Weis, Martin; Otsuka, Takako; Taguchi, Dai; Manaka, Takaaki; Iwamoto, Mitsumasa

    2015-04-21

    Organic light-emitting diode (OLED) displays using flexible substrates have many attractive features. Since transparent conductive oxides do not fit the requirements of flexible devices, conductive polymer poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonate) (PEDOT:PSS) has been proposed as an alternative. The charge injection and accumulation in OLED devices with PEDOT:PSS anodes are investigated and compared with indium tin oxide anode devices. Higher current density and electroluminescence light intensity are achieved for the OLED device with a PEDOT:PSS anode. The electric field induced second-harmonic generation technique is used for direct observation of temporal evolution of electric fields. It is clearly demonstrated that the improvement in the device performance of the OLED device with a PEDOT:PSS anode is associated with the smooth charge injection and accumulation.

  2. Improved electrospinning processing of PU/PEDOT:PSS for electronic textile applications

    NASA Astrophysics Data System (ADS)

    Evke, Erin; Clippinger, Aaron; Spackman, Clayson; Samuel, Johnson; Ozisik, Rahmi

    Poly(3,4-ethylenedioxythiophene)/poly(4-styrenesulfonate), PEDOT:PSS, is an electrically conductive polymer used in electronic textile (e-textile) applications, such as eletrochromic textiles, strain sensors, and resistive heaters. In the current study, PEDOT:PSS is blended with varying concentrations of polyurethane (PU) to investigate the flexibility of PU/PEDOT:PSS fibers that are produced via a modified electrospinning process where the jet is collected close to the tip of the needle, thereby, enabling the collection of straight fibers by a rotating spool. The electrical conductivity and mechanical properties of PU/PEDOT:PSS fibers are characterized to understand the effect of PU concentration and the processing parameters. This material is based upon work supported by the National Science Foundation under Grant No. CMMI-1538730.

  3. Enhanced optical and electrical properties of PEDOT:PSS/Gold nanocomposite system

    NASA Astrophysics Data System (ADS)

    Thappily, Praveen; Shiju, K.

    2014-10-01

    In this paper, we report modification of the electrical and optical properties of widely used transparent conducting polymer, PEDOT:PSS by the incorporation of gold nanoparticles (Au NPs) synthesized using aloe barbadensis leaf extract as reducing agent. The variation of workfunction of the PEDOT:PSS with Au Nanoparticles content is investigated and it has been seen that the work function of PEDOT:PSS can be tuned by incorporating nanoparticles. Further the optical absorption of the composite is found to be increasing considerably in the visible region. It has been demonstrated that there exists an optimum weight percentage of Au NPs for the composite formation with highest workfunction and enhanced light absorption in the visible region than pristine PEDOT:PSS.

  4. Aromatic sulfide/sulfone polymer production

    SciTech Connect

    Scoggins, L.E.; Hoover, K.C.; Shang, W.W.

    1991-05-14

    This patent describes a process for the production of aromatic sulfide/sulfone polymer. It comprises: contacting at least one lactam, at least one alkali metal hydrosulfide, water, and at least one base selected from the group consisting of alkali metal hydroxides and mixtures of alkali metal hydroxides with alkali metal carbonates under reaction conditions of time and temperature sufficient to produce a mixture containing a complex which comprises the at least one alkali metal hydrosulfide and contacting the mixture produced with a least one dihaloaromatic sulfone under polymerization conditions for a period of time sufficient to form an aromatic sulfide/sulfone polymer.

  5. Enhanced charge transport in highly conducting PEDOT-PSS films after acid treatment

    NASA Astrophysics Data System (ADS)

    Shiva, V. Akshaya; Bhatia, Ravi; Menon, Reghu

    The high electrical conductivity, good stability, high strength, flexibility and good transparency of poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT-PSS), make it useful for many applications including polymeric anodes for organic photovoltaics, light-emitting diodes, flexible electrodes, supercapacitors, electrochromic devices, field-effect transistors and antistatic-coatings. However, the electrical conductivity of PEDOT-PSS has to be increased significantly for replacement of indium tin oxide (ITO) as the transparent electrode in optoelectronic devices. The as prepared (pristine) PEDOT-PSS film prepared from the PEDOT-PSS aqueous solution usually has conductivity below 1Scm-1, remarkably lower than ITO. Significant conductivity enhancement has been observed on transparent and conductive PEDOT-PSS films after a treatment with inorganic acids. Our study investigates the charge transport in pristine and H2SO4, HNO3, HCl treated PEDOT-PSS films. We have treated the films with various concentrations of acids to probe the effect of the acid treatment on the conduction mechanism. The study includes the measurement of dc and electric field dependent conductivity of films in the temperature range of 4.2K-300K. We have also performed magneto-resistance measurements in the range of 0-5T. An enhancement by a factor of~103 has been observed in the room temperature conductivity. The detailed magneto-transport studies explain the various mechanisms for the conductivity enhancement observed.

  6. Characterizing hydrocarbon sulfonates and utilization of hydrocarbon sulfonates in oil recovery

    SciTech Connect

    Glinsmann, G.R.; Hedges, J.H.

    1982-05-18

    A method for determining the average equivalent weight of hydrocarbon sulfonates and the optimal salinity and unique salinity of surfactant systems containing such hydrocarbon sulfonates is based on the discovery that the average equivalent weights of hydrocarbon sulfonates vary inversely and linearly as the optimal salinities and unique salinities of surfactant systems containing such hydrocarbon sulfonates vary. Methods of preparing surfactant systems for the displacement of oil from subterranean reservoirs and for the displacement of oil from subterranean reservoirs, based on the above-mentioned relationships, are also disclosed.

  7. Chlorine resistant desalination membranes based on directly sulfonated poly(arylene ether sulfone) copolymers

    DOEpatents

    McGrath, James E.; Park, Ho Bum; Freeman, Benny D.

    2011-10-04

    The present invention provides a membrane, kit, and method of making a hydrophilic-hydrophobic random copolymer membrane. The hydrophilic-hydrophobic random copolymer membrane includes a hydrophilic-hydrophobic random copolymer. The hydrophilic-hydrophobic random copolymer includes one or more hydrophilic monomers having a sulfonated polyarylsulfone monomer and a second monomer and one or more hydrophobic monomers having a non-sulfonated third monomer and a fourth monomer. The sulfonated polyarylsulfone monomer introduces a sulfonate into the hydrophilic-hydrophobic random copolymer prior to polymerization.

  8. Direct methanol fuel cell performance using sulfonated poly (arylene ether sulfone) random copolymers as electrolytes.

    SciTech Connect

    Zawodzinski, T. A. , Jr.; Zelenay, P.; Hickner, M.; Wang, F.; McGrath, James E.; Pivovar, B. S.

    2001-01-01

    Sulfonated poly(arylene ether sulfone) random copolymers are a new series of sulfonic acid containing polymers that have shown promise as fuel cell electrolytes. Here, we report on direct methanol fuel cell (DMFC) performance of this class of polymers at sulfonation levels ranging from 40 to 60% (monomer basis). The DMFC performance of these polymers is compared to that of Nafion 117, the long standing standard in fuel cell testing. These polymers show a higher selectivity for protons over methanol for all the sulfonation levels tested, with the 40% sulfonated polymer showing 2.5 times the selectivity of Nafion. While the higher sulfonated forms (50 and 60%) did show a higher selectivity, only the lower sulfonation levels (40 and 45%) have shown improved performance in DMFC testing. The results of these experiments will be discussed in terms of the relevant test conditions, and experimentally determined membrane properties. The relevant DMFC properties of these polymers will be discussed in terms of sulfonation level and compared to those of Nafion 117.

  9. Synthesis of sulfonate analogs of bile acids.

    PubMed

    Kihira, K; Mikami, T; Ikawa, S; Okamoto, A; Yoshii, M; Miki, S; Mosbach, E H; Hoshita, T

    1992-04-01

    Sulfonate analogs of C23 and C24 bile acids were synthesized from norcholic, norchenodeoxycholic, norursodeoxycholic, nordeoxycholic, norhyodeoxycholic, cholic, deoxycholic, hyodeoxycholic, and lithocholic acids. The principal reactions used were (1) reduction of the bile acids with NaBH4 to the corresponding bile alcohols, (2) selective tosylation of the terminal hydroxyl group, (3) iodination of the tosyl esters with NaI, and (4) treatment of the iodides with Na2SO3 to form the sulfonate analogs of the bile acids. The sulfonate analogs showed polarity similar to that of taurine-conjugated bile acids on thin-layer chromatography. The carbon 13 nuclear magnetic resonance spectral data for the sulfonate analogs were tabulated.

  10. Crystal structure of zwitterionic bisimidazolium sulfonates

    NASA Astrophysics Data System (ADS)

    Kohmoto, Shigeo; Okuyama, Shinpei; Yokota, Nobuyuki; Takahashi, Masahiro; Kishikawa, Keiki; Masu, Hyuma; Azumaya, Isao

    2012-05-01

    Crystal structures of three zwitterionic bisimidazolium salts 1-3 in which imidazolium sulfonate moieties were connected with aromatic linkers, p-xylylene, 4,4'-dimethylenebiphenyl, and phenylene, respectively, were examined. The latter two were obtained as hydrates. An S-shaped molecular structure in which the sulfonate moiety was placed on the imidazolium ring was observed for 1. A helical array of hydrated water molecules was obtained for 2 while a linear array of hydrated water molecules was observed for 3.

  11. PssP2 Is a Polysaccharide Co-Polymerase Involved in Exopolysaccharide Chain-Length Determination in Rhizobium leguminosarum

    PubMed Central

    Marczak, Małgorzata; Matysiak, Paulina; Kutkowska, Jolanta; Skorupska, Anna

    2014-01-01

    Production of extracellular polysaccharides is a complex process engaging proteins localized in different subcellular compartments, yet communicating with each other or even directly interacting in multicomponent complexes. Proteins involved in polymerization and transport of exopolysaccharide (EPS) in Rhizobium leguminosarum are encoded within the chromosomal Pss-I cluster. However, genes implicated in polysaccharide synthesis are common in rhizobia, with several homologues of pss genes identified in other regions of the R. leguminosarum genome. One such region is chromosomally located Pss-II encoding proteins homologous to known components of the Wzx/Wzy-dependent polysaccharide synthesis and transport systems. The pssP2 gene encodes a protein similar to polysaccharide co-polymerases involved in determination of the length of polysaccharide chains in capsule and O-antigen biosynthesis. In this work, a mutant with a disrupted pssP2 gene was constructed and its capabilities to produce EPS and enter into a symbiotic relationship with clover were studied. The pssP2 mutant, while not altered in lipopolysaccharide (LPS), displayed changes in molecular mass distribution profile of EPS. Lack of the full-length PssP2 protein resulted in a reduction of high molecular weight EPS, yet polymerized to a longer length than in the RtTA1 wild type. The mutant strain was also more efficient in symbiotic performance. The functional interrelation between PssP2 and proteins encoded within the Pss-I region was further supported by data from bacterial two-hybrid assays providing evidence for PssP2 interactions with PssT polymerase, as well as glycosyltransferase PssC. A possible role for PssP2 in a complex involved in EPS chain-length determination is discussed. PMID:25268738

  12. In-situ characterization of electrochromism based on ITO/PEDOT:PSS towards preparation of high performance device

    NASA Astrophysics Data System (ADS)

    Xue-Jin, Wang; Zheng-Fei, Guo; Jing-Yu, Qu; Kun, Pan; Zheng, Qi; Li, Hong

    2016-02-01

    Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is usually sandwiched between indium tin oxide (ITO) and a functional polymer in order to improve the performance of the device. However, because of the strong acidic nature of PEDOT:PSS, the instability of ITO/PEDOT:PSS interface is also observed. The mechanism of degradation of the device remains is unclear and needs to be further studied. In this article, we investigate the in-situ electrochromism of PEDOT:PSS to disclose the cause of the degradation. X-ray photoelectron spectroscopy (XPS) was used to characterize the PEDOT:PSS films, as well as the PEDOT:PSS plus polyethylene glycol (PEG) films with and without indium ions. The electrochromic devices (ECD) based on PEDOT:PSS and PEG with and without indium ions are carried out by in-situ micro-Raman and laser reflective measurement (LRM). For comparison, ECD based on PEDOT:PSS and PEG films with LiCl, KCl, NaCl or InCl3 are also investigated by LRM. The results show that PEDOT:PSS is further reduced when negatively biased, and oxidized when positively biased. This could identify that PEDOT:PSS with indium ions from PEDOT:PSS etching ITO will lose dopants when negatively biased. The LRM shows that the device with indium ions has a stronger effect on the reduction property of PEDOT:PSS-PEG film than the device without indium ions. The contrast of the former device is 44%, that of the latter device is about 3%. The LRM also shows that the contrasts of the device based on PEDOT:PSS+PEG with LiCl, KCl, NaCl, InCl3 are 30%, 27%, 15%, and 18%, respectively. Project supported by the National High Technology Research and Development Program of China (Grant No. 2015AA034201) and the Chinese Universities Scientific Fund (Grant No. 2015LX002).

  13. Total dynamic response of a PSS vehicle negotiating asymmetric road excitations

    NASA Astrophysics Data System (ADS)

    Zhu, Jian Jun; Khajepour, Amir; Esmailzadeh, Ebrahim

    2012-12-01

    A planar suspension system (PSS) is a novel automobile suspension system in which an individual spring-damper strut is implemented in both the vertical and longitudinal directions, respectively. The wheels in a vehicle with such a suspension system can move back and forth relative to the chassis. When a PSS vehicle experiences asymmetric road excitations, the relative longitudinal motion of wheels with respect to the chassis in two sides of the same axle are not identical, and thus the two wheels at one axle will not be aligned in the same axis. The total dynamic responses, including those of the bounce, pitch and the roll of the PSS vehicle, to the asymmetric road excitation may exhibit different characteristics from those of a conventional vehicle. This paper presents an investigation into the comprehensive dynamic behaviour of a vehicle with the PSS, in such a road condition, on both the straight and curved roads. The study was carried out using an 18 DOF full-car model incorporating a radial-spring tyre-ground contact model and a 2D tyre-ground dynamic friction model. Results demonstrate that the total dynamic behaviour of a PSS vehicle is generally comparable with that of the conventional vehicle, while PSS exhibits significant improvement in absorbing the impact forces along the longitudinal direction when compared to the conventional suspension system. The PSS vehicle is found to be more stable than the conventional vehicle in terms of the directional performance against the disturbance of the road potholes on a straight line manoeuvre, while exhibiting a very similar handling performance on a curved line.

  14. Investigating the chemical mist deposition technique for poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) on textured crystalline-silicon for organic/crystalline-silicon heterojunction solar cells

    NASA Astrophysics Data System (ADS)

    Hossain, Jaker; Ohki, Tatsuya; Ichikawa, Koki; Fujiyama, Kazuhiko; Ueno, Keiji; Fujii, Yasuhiko; Hanajiri, Tatsuro; Shirai, Hajime

    2016-03-01

    Chemical mist deposition (CMD) of poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) was investigated in terms of cavitation frequency f, solvent, flow rate of nitrogen, substrate temperature Ts, and substrate dc bias Vs as variables for efficient PEDOT:PSS/crystalline silicon (c-Si) heterojunction solar cells. The high-speed-camera and differential mobility analysis characterizations revealed that the average size and flux of PEDOT:PSS mist depend on f, type of solvent, and Vs. Film deposition occurred when positive Vs was applied to the c-Si substrate at Ts of 30-40 °C, whereas no deposition of films occurred with negative Vs, implying that the film is deposited mainly from negatively charged mist. The uniform deposition of PEDOT:PSS films occurred on textured c-Si(100) substrates by adjusting Ts and Vs. The adhesion of CMD PEDOT:PSS film to c-Si was greatly enhanced by applying substrate dc bias Vs compared with that of spin-coated film. The CMD PEDOT:PSS/c-Si heterojunction solar cell devices on textured c-Si(100) in 2 × 2 cm2 exhibited a power conversion efficiency η of 11.0% with better uniformity of the solar cell parameters. Furthermore, η was increased to 12.5% by adding an AR coating layer of molybdenum oxide MoOx formed by CMD. These findings suggest that CMD with negatively charged mist has great potential for the uniform deposition of organic and inorganic materials on textured c-Si substrates by suitably adjusting Ts and Vs.

  15. Primary biodegradation of linear alkyltoluene and alkylbenzene sulfonates.

    PubMed

    Singh, M; Satish, S

    1989-01-01

    Studies on the primary biodegradation of linear dodecylbenzene sulfonate, linear dodecyltoluene sulfonate, linear C(10-14) benzene sulfonate, linear C(10-14) toluene sulfonate, commercial samples of linear C(10-14) benzene sulfonate and branched dodecylbenzene sulfonate (DDBS) were carried out using a microbial culture developed from garden soil. Results show that linear alkyl toluene (LAT) is as degradable as linear alkylbenzene (LAB) in 7 days. However, a slower rate of degradation was noted with LAT. Various distributions of the positional isomers of the phenyl ring in the alkane chain of C(10-14) LAB showed no change in the pattern of primary biodegradation.

  16. Co-ordinated Design of AVR-PSS Using Multi Objective Genetic Algorithm

    NASA Astrophysics Data System (ADS)

    Selvabala, B.; Devaraj, D.

    Automatic Voltage Regulator (AVR) regulates the generator terminal voltage by controlling the amount of current supplied to the generator field winding by the exciter. Power system stabilizer (PSS) is installed with AVR to damp the low frequency oscillations in power system by providing a supplementary signal to the excitation system. Optimal tuning of AVR controller and PSS parameters is necessary for the satisfactory operation of the power system. When applying tuning method to obtain the optimal controller parameters individually, AVR improves the voltage regulation of the system and PSS improves the damping of the system. Simultaneous tuning of AVR and PSS is necessary to obtain better both voltage regulation and oscillation damping in the system. This paper deals with the optimal tuning of AVR controller and PSS parameters in the synchronous machine. The problem of obtaining the optimal controller parameters is formulated as an optimization problem and Multi-Objective Genetic Algorithm (MOGA) is applied to solve the optimization problem. The suitability of the proposed approach has been demonstrated through computer simulation in a Single Machine Infinite Bus (SMIB) system.

  17. Charge and spin transport in PEDOT:PSS nanoscale lateral devices.

    PubMed

    de Oliveira, Thales V A G; Gobbi, Marco; Porro, José M; Hueso, Luis E; Bittner, Alexander M

    2013-11-29

    The electrical transport of the highly conductive poly-(3,4-ethylenedioxythiophene):poly(styrenesulfonic acid) (PEDOT:PSS) is investigated with Ohmic and spin-polarized tunnel contacts at nanoscale lateral dimensions. Temperature-dependent charge transport measurements reveal that electrical conductivity scales non-linearly as a function of electrode spacing, which is attributed to the localization of carriers induced by the disorder introduced by the PSS polyelectrolyte. In addition, we demonstrate the integration of this conducting polymer in nanoscale lateral spin-valve devices by increasing the pH of the PEDOT:PSS solution. We present charge and magnetotransport measurement results of NiFe/AlOx/PEDOT:PSS/AlOx/NiFe lateral structures for various thicknesses of the alumina tunnel barriers. We discuss the absence of magnetoresistance of our spin valves within the framework of Valet-Fert theory, and estimate an upper limit for the spin lifetime of carriers in PEDOT:PSS to τsf ≤ 50 ns. PMID:24177495

  18. Susceptibility of Candida albicans to new synthetic sulfone derivatives.

    PubMed

    Staniszewska, Monika; Bondaryk, Małgorzata; Ochal, Zbigniew

    2015-02-01

    The influence of halogenated methyl sulfones, i.e. bromodichloromethyl-4-chloro-3-nitrophenyl sulfone (named halogenated methyl sulfone 1), dichloromethyl-4-chloro-3-nitrophenyl sulfone (halogenated methyl sulfone 2), and chlorodibromomethyl-4-hydrazino-3-nitrophenyl sulfone (halogenated methyl sulfone 3), on cell growth inhibition, aspartic protease gene (SAP4-6) expression, adhesion to epithelium, and filamentation was investigated. Antifungal susceptibility of the halogenated methyl sulfones was determined with the M27-A3 protocol in the range of 16-0.0313 µg/mL. Adherence to Caco-2 cells was performed in 24-well plates; relative quantification was normalized against ACT1 in cells after 18 h of growth in YEPD and on Caco-2 cells. SAP4-6 expression was analyzed using RT-PCR. Structure-activity relationship studies suggested that halogenated methyl sulfone 1 containing bromodichloromethyl or dichloromethyl function at C-4 (halogenated methyl sulfone 2) of the phenyl ring showed the best activity (100% cell inhibition at 0.5 µg/mL), while hydrazine at C-1 (halogenated methyl sulfone 3) reduced the sulfone potential (100% = 4 µg/mL). SAP4-6 were up- or down-regulated depending on the strains' genetic background and the substitutions on the phenyl ring. Halogenated methyl sulfone 2 repressed germination and affected adherence to epithelium (P ≤ 0.05). The tested halogenated methyl sulfones interfered with the adhesion of Candida albicans cells to the epithelial tissues, without affecting their viability after 90 min of incubation. The mode of action of the halogenated methyl sulfones was attributed to the reduced virulence of C. albicans. SAP5 and SAP6 contribute to halogenated methyl sulfones resistance. Thus, halogenated methyl sulfones can inhibit biofilm formation due to their interference with adherence and with the yeast-to-hyphae transition.

  19. Direct AFM force measurements between air bubbles in aqueous polydisperse sodium poly(styrene sulfonate) solutions: effect of collision speed, polyelectrolyte concentration and molar mass.

    PubMed

    Browne, Christine; Tabor, Rico F; Grieser, Franz; Dagastine, Raymond R

    2015-07-01

    Interactions between colliding air bubbles in aqueous solutions of polydisperse sodium poly(styrene sulfonate) (NaPSS) using direct force measurements were studied. The forces measured with deformable interfaces were shown to be more sensitive to the presence of the polyelectrolytes when compared to similar measurements using rigid interfaces. The experimental factors that were examined were NaPSS concentration, bubble collision velocity and polyelectrolyte molar mass. These measurements were then compared with an analytical model based on polyelectrolyte scaling theory in order to explain the effects of concentration and bubble deformation on the interaction between bubbles. Typically structural forces from the presence of monodisperse polyelectrolyte between interacting surfaces may be expected, however, it was found that the polydispersity in molar mass resulted in the structural forces to be smoothed and only a depletion interaction was able to be measured between interacting bubbles. It was found that an increase in number density of NaPSS molecules resulted in an increase in the magnitude of the depletion interaction. Conversely this interaction was overwhelmed by an increase in the fluid flow in the system at higher bubble collision velocities. Polymer molar mass dispersity plays a significant role in the interactions present between the bubbles and has implications that also affect the polyelectrolyte overlap concentration of the solution. Further understanding of these implications can be expected to play a role in the improvement in operations in such fields as water treatment and mineral processing where polyelectrolytes are used extensively.

  20. Enhanced conductivity of poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) film by acid treatment for indium tin oxide-free organic solar cells

    NASA Astrophysics Data System (ADS)

    Lin, Chun-Chiao; Huang, Chih-Kuo; Hung, Yu-Chieh; Chang, Mei-Ying

    2016-08-01

    An acid treatment is used in the enhancement of the conductivity of the conducting polymer poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) thin film, which is often used as the anode in organic solar cells. There are three types of acid treatment for PEDOT:PSS thin film: hydrochloric, sulfuric, and phosphoric acid treatments. In this study, we examine and compare these three ways with each other for differences in conductivity. Hydrochloric acid results in the highest conductivity enhancement, from 0.3 to 1109 S/cm. We also discuss the optical transmittance, conductivity, surface roughness, surface morphology, and stability, as well as the factors that can influence device efficiency. The devices are fabricated using an acid-treated PEDOT:PSS thin film as the anode. The highest power conversion efficiency was 1.32%, which is a large improvement over that of the unmodified organic solar cell (0.21%). It is comparable to that obtained when using indium tin oxide (ITO) as an electrode, ca. 1.46%.

  1. Highly stable multi-wall carbon nanotubes@poly(3,4-ethylenedioxythiophene)/poly(styrene sulfonate) core-shell composites with three-dimensional porous nano-network for electrochemical capacitors

    NASA Astrophysics Data System (ADS)

    Zhou, Haihan; Han, Gaoyi; Chang, Yunzhen; Fu, Dongying; Xiao, Yaoming

    2015-01-01

    A facile and feasible electrochemical polymerization method has been used to construct the multi-wall carbon nanotubes@poly(3,4-ethylenedioxythiophene)/poly(styrene sulfonate) (MWCNTs@PEDOT/PSS) core-shell composites with three-dimensional (3D) porous nano-network microstructure. The composites are characterized with Fourier transform infrared spectroscopy, scanning electron microscope, and transmission electron microscopy. This special core-shell nanostructure can significantly reduce the ions diffusion distance and the 3D porous nano-network microstructure effectively enlarges the electrode/electrolyte interface. The electrochemical tests including cyclic voltammetry, galvanostatic charge/discharge measurements, and electrochemical impedance spectroscopy tests are performed, the results manifest the MWCNTs@PEDOT/PSS core-shell composites have superior capacitive behaviors and excellent cyclic stability, and a high areal capacitance of 98.1 mF cm-2 is achieved at 5 mV s-1 cyclic voltammetry scan. Furthermore, the MWCNTs@PEDOT/PSS composites exhibit obviously superior capacitive performance than that of PEDOT/PSS and PEDOT/Cl electrodes, indicating the effective composite of MWCNTs and PEDOT noticeably boosts the capacitive performance of PEDOT-based electrodes for electrochemical energy storage. Such a highly stable core-shell 3D network structural composite is very promising to be used as electrode materials for the high-performance electrochemical capacitors.

  2. Waterflooding employing mixtures of sulfonate surfactants

    SciTech Connect

    Savins, J.G.; Waite, J.M.; Burdyn, R.F.

    1980-11-04

    A new waterflooding process is described in which at least a portion of the injected fluid comprises a viscous aqueous liquid having a monovalent salt salinity within the range of 1.5 to 4.0% by wt and containing first and second sulfonate surfactants. The first surfactant is a petroleum sulfonate having a relatively broad molecular weight distribution and the second surfactant is a synthetic alkyl or alkylaryl sulfonate having a molecular weight distribution narrower than that of the first surfactant. The first and second surfactants are present in the aqueous liquid in relative amounts such that the ratio of the concentration of the first surfactant to the concentration of the second surfactant is within the range of 1:3 to 1:1. The thickened aqueous liquid containing the above described multicomponent surfactant system also contains a water-soluble C3-C6 aliphatic alcohol. 11 claims.

  3. Simulation study of sulfonate cluster swelling in ionomers

    NASA Astrophysics Data System (ADS)

    Allahyarov, Elshad; Taylor, Philip L.; Löwen, Hartmut

    2009-12-01

    We have performed simulations to study how increasing humidity affects the structure of Nafion-like ionomers under conditions of low sulfonate concentration and low humidity. At the onset of membrane hydration, the clusters split into smaller parts. These subsequently swell, but then maintain constant the number of sulfonates per cluster. We find that the distribution of water in low-sulfonate membranes depends strongly on the sulfonate concentration. For a relatively low sulfonate concentration, nearly all the side-chain terminal groups are within cluster formations, and the average water loading per cluster matches the water content of membrane. However, for a relatively higher sulfonate concentration the water-to-sulfonate ratio becomes nonuniform. The clusters become wetter, while the intercluster bridges become drier. We note the formation of unusual shells of water-rich material that surround the sulfonate clusters.

  4. Reliability, Validity and Preliminary Hypothesis Tests for the English Version of the Psychological Strain Scales (PSS)1

    PubMed Central

    Zhang, Jie; Lyu, Juncheng

    2014-01-01

    Background The original Psychological Strain Scales (PSS) was published with data from a sample of a Chinese population, which consisted of four strain scales: value strain, aspiration strain, deprivation strain, coping strain. This study aims to validate and develop the English version of the PSS instrument. Method Together with the PSS, Moos’s Coping Response Inventory (CRI), Spielberger Trait-Anxiety scale, CES-D depression scale, and the NCS suicidal behavior scales were administered in a survey to a sample (N=280) of American college students. Item-total statistics, Cronbach’s Alpha, Guttman Split-Half coefficient, factor analyses, correlation analysis and t tests were applied to test the reliability and validity of the English version of the PSS. Univariate and multivariable regression analyses were operated to know how extent the PSS predicts psychopathology such as anxiety, depression and suicidal behaviors. Results Cronbach’s Alpha coefficient of PSS was 0.936. The Split-Half Coefficient of PSS was 0.839. The reliability of the PSS was excellent. The factor analysis results demonstrated strong construct validity of each scale. The criterion validity and the discriminant validity were both excellent for the English version of PSS instrument. Conclusions With the excellent scores on both reliability and validity, the English version of the PSS scales can be an excellent measurement for estimating the psychological strain levels of American college students as well as predicting their psychopathology. The PSS can be applicable for research to evaluate and predict suicidal behaviors and mental disorders. PMID:24856556

  5. Characterization of doped PEDOT: PSS and its influence on the performance and degradation of organic solar cells

    NASA Astrophysics Data System (ADS)

    Singh, Vinamrita; Arora, Swati; Arora, Manoj; Sharma, Vishal; Tandon, R. P.

    2014-04-01

    The present work is a detailed study of the optical, morphological and electrical properties of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate), PEDOT:PSS, films doped with ethylene glycol (EG) and multi-walled carbon nanotubes (MWCNT). The conductivity of PEDOT:PSS films doped with EG and MWCNT is higher than pristine PEDOT:PSS film. The optical transparency of PEDOT:PSS film decreases insignificantly after addition of MWCNT and EG. The films were further studied using atomic force microscopy, x-ray diffraction, Raman spectroscopy and Kelvin probe work function measurement, after which films of PEDOT:PSS with EG and MWCNT were optimized for the fabrication of solar cells. The optimized film was used as a hole extracting layer in a typical ITO/PEDOT:PSS/P3HT:PCBM/Al solar cell. The suitable concentration for an optimized film was found to be 4% MWCNT and 1:4 ratio of EG to PEDOT:PSS. The performance of the device with doped PEDOT:PSS was found to improve in terms of short circuit current density (JSC) and efficiency (η). The solar cell with a doped PEDOT:PSS layer showed higher JSC and η due to the increase in the interchains among PEDOT chains along with the introduction of MWCNT channels in PEDOT:PSS matrix. The degradation behavior of the cells was studied and it was found that both pristine and doped PEDOT:PSS cells showed similar trends of degradation. The performance degradation with time was also studied under variable environmental conditions, which showed different aging rates for the two devices.

  6. Solvent-induced changes in PEDOT:PSS films for organic electrochemical transistors

    SciTech Connect

    Zhang, Shiming; Kumar, Prajwal; Nouas, Amel Sarah; Fontaine, Laurie; Tang, Hao; Cicoira, Fabio

    2015-01-01

    Organic electrochemical transistors based on the conducting polymer poly(3,4-ethylenedioxythiophene) doped with poly(styrenesulfonate) (PEDOT:PSS) are of interest for several bioelectronic applications. In this letter, we investigate the changes induced by immersion of PEDOT:PSS films, processed by spin coating from different mixtures, in water and other solvents of different polarities. We found that the film thickness decreases upon immersion in polar solvents, while the electrical conductivity remains unchanged. The decrease in film thickness is minimized via the addition of a cross-linking agent to the mixture used for the spin coating of the films.

  7. A way for studying the impact of PEDOT:PSS interface layer on carrier transport in PCDTBT:PC{sub 71}BM bulk hetero junction solar cells by electric field induced optical second harmonic generation measurement

    SciTech Connect

    Ahmad, Zubair Abdullah, Shahino Mah; Sulaiman, Khaulah; Taguchi, Dai; Iwamoto, Mitsumasa

    2015-04-28

    Electric-field-induced optical second-harmonic generation (EFISHG) measurement was employed to study the impact of poly(3,4-ethylenedioxythiophene)-polystyrene sulfonate (PEDOT:PSS) interface layer on the carrier transport mechanism of the PCDTBT:PC{sub 71}BM bulk heterojunction (BHJ) organic solar cells (OSCs). We revealed that the electric fields in the PCDTBT and PC{sub 71}BM were allowed to be measured individually by choosing fundamental laser wavelengths of 1000 nm and 1060 nm, respectively, in dark and under illumination. The results showed that the direction of the internal electric fields in the PCDTBT:PC{sub 71}BM BHJ layer is reversed by introducing the PEDOT:PSS layer, and this results in longer electron transport time in the BHJ layer. We conclude that TR-EFISHG can be used as a novel way for studying the impact of interfacial layer on the transport of electrons and holes in the bulk-heterojunction OSCs.

  8. 40 CFR 721.1625 - Alkylbenzene sulfonate, amine salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Alkylbenzene sulfonate, amine salt... Substances § 721.1625 Alkylbenzene sulfonate, amine salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as alkylbenzene sulfonate,...

  9. 40 CFR 721.10035 - Alkylbenzene sulfonate (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Alkylbenzene sulfonate (generic). 721... Substances § 721.10035 Alkylbenzene sulfonate (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as alkylbenzene sulfonate...

  10. 40 CFR 721.10035 - Alkylbenzene sulfonate (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Alkylbenzene sulfonate (generic). 721... Substances § 721.10035 Alkylbenzene sulfonate (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as alkylbenzene sulfonate...

  11. 40 CFR 721.1625 - Alkylbenzene sulfonate, amine salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Alkylbenzene sulfonate, amine salt... Substances § 721.1625 Alkylbenzene sulfonate, amine salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as alkylbenzene sulfonate,...

  12. 21 CFR 173.395 - Trifluoromethane sulfonic acid.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Trifluoromethane sulfonic acid. 173.395 Section... HUMAN CONSUMPTION Specific Usage Additives § 173.395 Trifluoromethane sulfonic acid. Trifluoromethane sulfonic acid has the empirical formula CF3SO3H (CAS Reg. No. 1493-13-6). The catalyst...

  13. 21 CFR 177.2500 - Polyphenylene sulfone resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyphenylene sulfone resins. 177.2500 Section 177... Components of Articles Intended for Repeated Use § 177.2500 Polyphenylene sulfone resins. The polyphenylene sulfone resins (CAS Reg. No. 31833-61-1) identified in paragraph (a) of this section may be safely used...

  14. 21 CFR 177.2500 - Polyphenylene sulfone resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyphenylene sulfone resins. 177.2500 Section 177... Components of Articles Intended for Repeated Use § 177.2500 Polyphenylene sulfone resins. The polyphenylene sulfone resins (CAS Reg. No. 31833-61-1) identified in paragraph (a) of this section may be safely used...

  15. 21 CFR 173.395 - Trifluoromethane sulfonic acid.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Trifluoromethane sulfonic acid. 173.395 Section... HUMAN CONSUMPTION Specific Usage Additives § 173.395 Trifluoromethane sulfonic acid. Trifluoromethane sulfonic acid has the empirical formula CF3SO3H (CAS Reg. No. 1493-13-6). The catalyst...

  16. 21 CFR 173.395 - Trifluoromethane sulfonic acid.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Trifluoromethane sulfonic acid. 173.395 Section... HUMAN CONSUMPTION Specific Usage Additives § 173.395 Trifluoromethane sulfonic acid. Trifluoromethane sulfonic acid has the empirical formula CF3SO3H (CAS Reg. No. 1493-13-6). The catalyst...

  17. 40 CFR 721.1625 - Alkylbenzene sulfonate, amine salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Alkylbenzene sulfonate, amine salt... Substances § 721.1625 Alkylbenzene sulfonate, amine salt. Link to an amendment published at 79 FR 34636, June... substance identified generically as alkylbenzene sulfonate, amine salt (PMN P-90-456) is subject...

  18. A dual-responsive superparamagnetic Fe 3O 4/Silica/PAH/PSS material used for controlled release of chemotherapeutic agent, keggin polyoxotungstate, PM-19

    NASA Astrophysics Data System (ADS)

    Xu, Rui; Sun, Guoying; Li, Qiuyu; Wang, Enbo; Gu, Jianmin

    2010-10-01

    A bicontrollable drug release system was developed by layer-by-layer assembly of poly(allylamine hydrochloride) (PAH)/sodium poly(styrene sulfonate) (PSS) multilayers onto a Fe 3O 4/SiO 2 composite core. The saturated magnetization of this system reaches up to 38.6 emu/g at RT, making targeting easily controlled by an external magnetic field. Meanwhile, the packing of the polyelectrolyte multilayers is sensitive to pH values, generating a pH-switch on-off mode for the release of loaded drugs. In this specific case, the release of a chemotherapeutic polyoxometalate K 7Ti 2W 10PO 40·6H 2O (PM-19) was tested. Transmission electron microscopy (TEM) was used to examine the nanostructure of the composite drug release system. UV-vis absorption was used to monitor the drug release. Fourier transform infrared (FTIR), Powder X-ray diffraction, and Elemental analyses were used to study the composition of tested systems. The structure and composition of the composite system was also studied using magnetism measurement and nitrogen adsorption-desorption.

  19. Resistive Switching Memory Phenomena in PEDOT PSS: Coexistence of Switchable Diode Effect and Write Once Read Many Memory.

    PubMed

    Nguyen, Viet Cuong; Lee, Pooi See

    2016-01-01

    We study resistive switching memory phenomena in conducting polymer PEDOT PSS. In the same film, there are two types of memory behavior coexisting; namely, the switchable diode effect and write once read many memory. This is the first report on switchable diode phenomenon based on conducting organic materials. The effect was explained as charge trapping of PEDOT PSS film and movement of proton. The same PEDOT PSS device also exhibits write once read many memory (WORM) phenomenon which arises due to redox reaction that reduces PEDOT PSS and renders it non-conducting. The revelation of these two types of memory phenomena in PEDOT PSS highlights the remarkable versatility of this conducting conjugated polymer. PMID:26806868

  20. Resistive Switching Memory Phenomena in PEDOT PSS: Coexistence of Switchable Diode Effect and Write Once Read Many Memory

    PubMed Central

    Nguyen, Viet Cuong; Lee, Pooi See

    2016-01-01

    We study resistive switching memory phenomena in conducting polymer PEDOT PSS. In the same film, there are two types of memory behavior coexisting; namely, the switchable diode effect and write once read many memory. This is the first report on switchable diode phenomenon based on conducting organic materials. The effect was explained as charge trapping of PEDOT PSS film and movement of proton. The same PEDOT PSS device also exhibits write once read many memory (WORM) phenomenon which arises due to redox reaction that reduces PEDOT PSS and renders it non-conducting. The revelation of these two types of memory phenomena in PEDOT PSS highlights the remarkable versatility of this conducting conjugated polymer. PMID:26806868

  1. Resistive Switching Memory Phenomena in PEDOT PSS: Coexistence of Switchable Diode Effect and Write Once Read Many Memory

    NASA Astrophysics Data System (ADS)

    Nguyen, Viet Cuong; Lee, Pooi See

    2016-01-01

    We study resistive switching memory phenomena in conducting polymer PEDOT PSS. In the same film, there are two types of memory behavior coexisting; namely, the switchable diode effect and write once read many memory. This is the first report on switchable diode phenomenon based on conducting organic materials. The effect was explained as charge trapping of PEDOT PSS film and movement of proton. The same PEDOT PSS device also exhibits write once read many memory (WORM) phenomenon which arises due to redox reaction that reduces PEDOT PSS and renders it non-conducting. The revelation of these two types of memory phenomena in PEDOT PSS highlights the remarkable versatility of this conducting conjugated polymer.

  2. Perfluorooctane sulfonate (PFOS) depletion in beef cattle

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Perfluorooctane sulfonate (PFOS) is an industrial chemical that is used as a surfactant in several manufactured consumer products but is also a breakdown product from other chemical surfactants. As a result of its extensive use, PFOS is ubiquitous in the environment and is often detected in biosoli...

  3. Sulfonated Polymerized Ionic Liquid Block Copolymers.

    PubMed

    Meek, Kelly M; Elabd, Yossef A

    2016-07-01

    The successful synthesis of a new diblock copolymer, referred to as sulfonated polymerized ionic liquid (PIL) block copolymer, poly(SS-Li-b-AEBIm-TFSI), is reported, which contains both sulfonated blocks (sulfonated styrene: SS) and PIL blocks (1-[(2-acryloyloxy)ethyl]-3-butylimidazolium: AEBIm) with both mobile cations (lithium: Li(+) ) and mobile anions (bis(trifluoromethylsulfonyl)imide: TFSI(-) ). Synthesis consists of polymerization via reversible addition-fragmentation chain transfer, followed by post-functionalization reactions to covalently attach the imidazolium cations and sulfonic acid anions to their respective blocks, followed by ion exchange metathesis resulting in mobile Li(+) cations and mobile TFSI(-) anions. Solid-state films containing 1 m Li-TFSI salt dissolved in ionic liquid result in an ion conductivity of >1.5 mS cm(-1) at 70 °C, where small-angle X-ray scattering data indicate a weakly ordered microphase-separated morphology. These results demonstrate a new ion-conducting block copolymer containing both mobile cations and mobile anions. PMID:27125600

  4. 21 CFR 573.600 - Lignin sulfonates.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food... accordance with the following prescribed conditions: (a) For the purpose of this section, the food additive... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Lignin sulfonates. 573.600 Section 573.600...

  5. 21 CFR 573.600 - Lignin sulfonates.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food... accordance with the following prescribed conditions: (a) For the purpose of this section, the food additive... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Lignin sulfonates. 573.600 Section 573.600...

  6. 21 CFR 573.600 - Lignin sulfonates.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food... accordance with the following prescribed conditions: (a) For the purpose of this section, the food additive... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Lignin sulfonates. 573.600 Section 573.600...

  7. Toxicity of pyrolysis gases from polyether sulfone

    NASA Technical Reports Server (NTRS)

    Hilado, C. J.; Olcomendy, E. M.

    1979-01-01

    A sample of polyether sulfone was evaluated for toxicity of pyrolysis gases, using the toxicity screening test method developed at the University of San Francisco. Animal response times were relatively short at pyrolysis temperatures of 600 to 800 C, with death occurring within 6 min. The principal toxicant appeared to be a compound other than carbon monoxide.

  8. Properties of polypyrrole doped with alkylbenzene sulfonates

    NASA Astrophysics Data System (ADS)

    Bay, Lasse; Skaarup, Steen; West, Keld; Mazur, Tanja; Joergensen, Ole; Rasmussen, Helle D.

    2001-07-01

    Conducting polymers such as polypyrrole (PPy) doped with large anionic detergents have high stability in aqueous systems. PPy can be reversibly oxidised and reduced electrochemically. The redox change of PPy is accompanied by a change in volume of the polymer. This is partly ascribed to take-up of ions and solvent molecules. This volume change can be used as a polymer actuator (artificial muscle) working in a narrow voltage range (less than 1 V). The properties of the PPy polymer are largely determined by the dopant ions and also by the deposition conditions and the substrate. A free-standing 10 micrometers thick film is prepared electrochemically at a constant current from an aqueous solution of pyrrole and sodium alkylbenzene sulfonate. The mechanical properties of the film (tensile strength and Young's modulus) and the reversible linear elongation between the oxidised and reduced states are measured. Alkylbenzene sulfonates with alkyl chain lengths between 1 and 22 carbon atoms are used as dopant anion. The films made with the different anions have highly different properties and are here compared to outline the influence of the size of the anion. A maximum in linear elongation is found for p-(n-octyl)benzene sulfonate and in conductivity for p-(n-butyl)benzene sulfonate.

  9. Measuring Malaysia School Resource Centers' Standards through iQ-PSS: An Online Management Information System

    ERIC Educational Resources Information Center

    Zainudin, Fadzliaton; Ismail, Kamarulzaman

    2010-01-01

    The Ministry of Education has come up with an innovative way to monitor the progress of 9,843 School Resource Centers (SRCs) using an online management information system called iQ-PSS (Quality Index of SRC). This paper aims to describe the data collection method and analyze the current state of SRCs in Malaysia and explain how the results can be…

  10. Growth and Characterization of PEDOT:PSS and Carbon Nanotube Composite Structures for Excitonic Solar Cells

    NASA Astrophysics Data System (ADS)

    Owens, Constance; Hettiarachchi, Chaminda; Mateo-Feliciano, Domingo; Hyde, Robert; Witanachchi, Sarath

    2013-03-01

    Harnessing solar energy is one of the most promising ways to tackle today's energy issues. Though solar cells are comprised of many different layers, our focus is on a single layer. The main goal of this study is to create thin film composite structures of poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS) and carbon nanotubes (CNT), more specifically with multiple wall carbon nanotubes (MWCNT) by employing a spray method that utilizes Bernoulli's principle. We believe that a spray method will produce a better uniform layer than other methods that are utilized for creating thin films. Uniformity within a thin film is of the upmost importance because as uniformity is improved, many properties are enhanced. PEDOT:PSS was mixed separately with both dimethylformamide (DMF) and water. By the Dektak 3030ST, a profilometer device, it was discovered that the PEDOT:PSS containing DMF dispersed better than the PEDOT:PSS mixed with water, thus creating a more uniform film. Also it is well known that CNTs possess many excellent properties that can make them very useful in the field of solar technology. In this study we also combine MWCNTs into our thin films to see how they affect thickness, transparency and conductivity by using the Lambda 950, a UV/VIS spectrometer, and a four point probe.

  11. Electrode patterning on PEDOT:PSS thin films by pulsed ultraviolet laser for touch panel screens

    NASA Astrophysics Data System (ADS)

    Tseng, Shih-Feng; Hsiao, Wen-Tse; Huang, Kuo-Cheng; Chiang, Donyau

    2013-07-01

    Laser dry etching by a laser driven direct writing apparatus has been extensively used for the micro- and nano-patterning on the solid surface. The purpose of this study is to pattern the PEDOT:PSS thin film coated on the soda-lime glass substrates by a nano-second pulsed ultraviolet laser processing system. The patterned PEDOT:PSS film structure provides the electrical isolation and prevents the electrical contact from each region for capacitive touch screens. The surface morphology, geometric dimension, and edge quality of ablated area after the variety of laser patternings were measured by a 3D confocal laser scanning microscope. After the single pulse laser irradiation, the ablation threshold of the PEDOT:PSS film conducted by the nano-second pulsed UV laser was determined to be 0.135±0.003 J/cm2. The single pulse laser interacted region and the ablated line depth increased with increasing the laser fluence. Moreover, the inner line width of ablated PEDOT:PSS films along the patterned line path increased with increasing the laser fluence but the shoulder width increased with decreasing fluence, respectively. The clean, smooth, and straight ablated edges were accomplished after the electrode patterning with the laser fluence of 1.7 J/cm2 and 90 % overlapping rate.

  12. Low-cost and broadband terahertz antireflection coatings based on DMSO-doped PEDOT/PSS.

    PubMed

    Yan, Fei; Parrott, Edward P J; Liu, Xu Dong; Pickwell-MacPherson, Emma

    2015-06-15

    We report the potential application of 6% dimethylsulfoxide (DMSO)-doped poly (3, 4-ethylenedioxythiophene)/poly (4-styrenesulfonate) (PEDOT/PSS) as a low cost and broadband terahertz (THz) antireflection coating based on the impedance matching effect. The reflected pulses from the quartz and silicon substrates are observed to change with the thickness of the PEDOT/PSS layer. Theoretical analysis based on an equivalent transmission line circuit model and FDTD computational simulations have been used to understand the experimental results. Excellent impedance matching is achieved by a ∼39-nm-thick 6% DMSO-doped PEDOT/PSS layer on quartz, and a ∼101-nm-thick 6% DMSO-doped PEDOT/PSS layer on silicon due to the almost-frequency-independent conductivity of the thin film between 0.3 and 2.5 THz. In the critical conditions, the normalized main pulse transmission remains as high as 74% and 64%, for the quartz and silicon substrates, respectively, significantly higher than the existing state of the art THz antireflection coatings. PMID:26076287

  13. Enhanced Performance and Stability in Polymer Photovoltaic Cells Using Ultraviolet-Treated PEDOT:PSS

    NASA Astrophysics Data System (ADS)

    Xu, Xue-Jian; Yang, Li-Ying; Tian, Hui; Qin, Wen-Jing; Yin, Shou-Gen; Zhang, Fengling

    2013-07-01

    We investigate the effects of ultraviolet (UV) irradiation treatment with varying irradiation intensities for different treatment times of poly(3, 4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) film on the performance and stability of polymer solar cells (PSCs) based on regioregular poly(3-hexylthiophene) (P3HT) and methanofullerene [6,6]-phenyl C61-butyric acid methyl ester (PCBM) blend. Ultraviolet-visible transmission spectra, x-ray photoelectron spectroscopy, contact angle measurement, atomic force microscopy and the Kelvin probe method are conducted to characterize the UV-treated PEDOT:PSS film. The results demonstrate that UV treatment can improve the power conversion efficiency (PCE) and stability of PSCs effectively. The best performance is achieved under 1200 μW/cm2 UV treatment for 50 min. Compared to the control device, the optimized device exhibits enhanced performance with a Voc of 0.59 V, Jsc of 12.3 mA/cm2, fill factor of 51%, and PCE of 3.64%, increased by 3.5%, 33%, 8.7% and 50%, respectively. The stability of the PSCs is enhanced by 2.5 times simply through the UV treatment on the PEDOT:PSS buffer layer. The improvement in the device performance and stability is attributed to the improvement in the wettability property and the increase in the work function of the PEDOT:PSS film by UV treatment, while the impact of UV treatment on the transparency of the PEDOT:PSS film is negligible. The strategy of using UV treatment to improve device performance and stability is attractive due to its simplicity, cost-effectiveness, and because it is suitable for large-scale commercial production.

  14. Fabrication of water-dispersible and highly conductive PSS-doped PANI/graphene nanocomposites using a high-molecular weight PSS dopant and their application in H2S detection.

    PubMed

    Cho, Sunghun; Lee, Jun Seop; Jun, Jaemoon; Kim, Sung Gun; Jang, Jyongsik

    2014-12-21

    This work describes the fabrication of poly(4-styrenesulfonic acid)-doped polyaniline/graphene (PSS-doped PANI/graphene) nanocomposites and their use as sensing elements for hydrogen sulfide (H2S) detection. PSS with a weight-average molecular weight (Mw) of 1.96 × 10(6) was synthesized using low-temperature free-radical polymerization. The PSS was used as both a doping agent and a binding agent for the polymerization of aniline monomers in a biphasic system (water-chloroform) at -50 °C. The high Mw of PSS resulted in relatively large particle sizes and smooth surfaces of the PSS-doped PANI. These physical characteristics, in turn, resulted in low interparticle resistance and high conductivity. In addition, the PSS allowed homogeneous dispersion of reduced graphene sheets through electrostatic repulsion. The prepared PSS-doped PANI/graphene solutions showed good compatibility with flexible poly(ethylene terephthalate) (PET) substrates, making them suitable for flexible sensor electrodes. Changes in the charge-transport properties, such as protonation level, conjugation length, crystalline structure, and charge-transfer resistance, of the electrode materials were the main factors influencing the electrical and sensor performance of the PSS-doped PANI-based electrodes. PSS-doped PANI/graphene composites containing 30 wt% graphene showed the highest conductivity (168.4 S cm(-1)) and the lowest minimum detection level (MDL) for H2S gas (1 ppm). This result is consistent with the observed improvements in charge transport in the electrode materials via strong π-π stacking interactions between the PANI and the graphene sheets.

  15. Fabrication of water-dispersible and highly conductive PSS-doped PANI/graphene nanocomposites using a high-molecular weight PSS dopant and their application in H2S detection

    NASA Astrophysics Data System (ADS)

    Cho, Sunghun; Lee, Jun Seop; Jun, Jaemoon; Kim, Sung Gun; Jang, Jyongsik

    2014-11-01

    This work describes the fabrication of poly(4-styrenesulfonic acid)-doped polyaniline/graphene (PSS-doped PANI/graphene) nanocomposites and their use as sensing elements for hydrogen sulfide (H2S) detection. PSS with a weight-average molecular weight (Mw) of 1.96 × 106 was synthesized using low-temperature free-radical polymerization. The PSS was used as both a doping agent and a binding agent for the polymerization of aniline monomers in a biphasic system (water-chloroform) at -50 °C. The high Mw of PSS resulted in relatively large particle sizes and smooth surfaces of the PSS-doped PANI. These physical characteristics, in turn, resulted in low interparticle resistance and high conductivity. In addition, the PSS allowed homogeneous dispersion of reduced graphene sheets through electrostatic repulsion. The prepared PSS-doped PANI/graphene solutions showed good compatibility with flexible poly(ethylene terephthalate) (PET) substrates, making them suitable for flexible sensor electrodes. Changes in the charge-transport properties, such as protonation level, conjugation length, crystalline structure, and charge-transfer resistance, of the electrode materials were the main factors influencing the electrical and sensor performance of the PSS-doped PANI-based electrodes. PSS-doped PANI/graphene composites containing 30 wt% graphene showed the highest conductivity (168.4 S cm-1) and the lowest minimum detection level (MDL) for H2S gas (1 ppm). This result is consistent with the observed improvements in charge transport in the electrode materials via strong π-π stacking interactions between the PANI and the graphene sheets.This work describes the fabrication of poly(4-styrenesulfonic acid)-doped polyaniline/graphene (PSS-doped PANI/graphene) nanocomposites and their use as sensing elements for hydrogen sulfide (H2S) detection. PSS with a weight-average molecular weight (Mw) of 1.96 × 106 was synthesized using low-temperature free-radical polymerization. The PSS was

  16. Highly branched sulfonated poly(fluorenyl ether ketone sulfone)s membrane for energy efficient vanadium redox flow battery

    NASA Astrophysics Data System (ADS)

    Yin, Bibo; Li, Zhaohua; Dai, Wenjing; Wang, Lei; Yu, Lihong; Xi, Jingyu

    2015-07-01

    A series of highly branched sulfonated poly (fluorenyl ether ketone sulfone)s (HSPAEK) are synthesized by direct polycondensation reactions. The HSPAEK with 8% degree of branching is further investigated as membrane for vanadium redox flow battery (VRFB). The HSPAEK membrane prepared by solution casting method exhibits smooth, dense and tough morphology. It possesses very low VO2+ permeability and high ion selectivity compared to those of Nafion 117 membrane. When applied to VRFB, this novel membrane shows higher coulombic efficiency (CE, 99%) and energy efficiency (EE, 84%) than Nafion 117 membrane (CE, 92% and EE, 78%) at current density of 80 mA cm-2. Besides, the HSPAEK membrane shows super stable CE and EE as well as excellent discharge capacity retention (83%) during 100 cycles life test. After being soaked in 1.5 mol L-1 VO2+ solution for 21 days, the weight loss of HSPAEK membrane and the amount of VO2+ reduced from VO2+ are only 0.26% and 0.7%, respectively, indicating the superior chemical stability of the membrane.

  17. Morphologies in Sulfonated Styrenic Pentablock Copolymer Membranes

    NASA Astrophysics Data System (ADS)

    Choi, Jae-Hong; Bramson, Matt; Winey, Karen I.

    2010-03-01

    Membranes of pentablock and triblock copolymers consisting of poly(tert-butyl styrene) (TBS), hydrogenated polyisoprene (HI), and partially sulfonated poly(styrene-ran-styrene sulfonate) (SS) were studied using small angle X-ray scattering (SAXS) and transmission electron microscopy (TEM). The TBS-HI-SS-HI-TBS pentablock and TBS-HI-SS triblock copolymer membranes exhibit anisotropic microphase separated morphologies. Because the pentablock and triblock copolymers can be expected to have complex morphologies, thermal annealing was conducted to promote well-defined morphologies. The annealed membranes exhibit stronger peaks and more high order reflections in SAXS patterns, as well as better defined microstructures in the TEM. Electron microcopy studies with various staining protocols are underway to establish the morphology of the pentablock copolymer membranes including the size and shape of the three microdomains (TBS, HI and SS). We gratefully acknowledge Kraton Polymers, Inc. for materials.

  18. Sorption of sodium dodecylbenzene sulfonate by montmorillonite.

    PubMed

    Yang, Kun; Zhu, Lizhong; Xing, Baoshan

    2007-01-01

    Sorption of linear alkylbenzene sulfonates by soils and sediments is an important process that may affect their fate, transport, toxicity and their application in remediation of contaminated soil and groundwater. In this study, batch experiments were conducted to elucidate the sorption of a widely used anionic surfactant, sodium dodecylbenzene sulfonate (SDBS), by montmorillonite. It was observed that: (i) SDBS was sorbed significantly by montmorillonite saturated with Ca(2+), but little by Na-saturated montmorillonite; (ii) the amount of SDBS sorbed by Ca(2+)-montmorillonite was enhanced by NaCl; and (iii) no significant intercalation of SDBS into Ca(2+)-montmorillonite was observed by X-ray diffraction (XRD) analysis. These results indicate that the removal of SDBS by Ca(2+)-montmorillonite was primarily attributed to the precipitation between DBS(-) and Ca(2+) in solution which was released from montmorillonite via cation exchange. These results will help us to understand the sorption behavior and environmental effects of anionic surfactants. PMID:16759775

  19. Sorption of sodium dodecylbenzene sulfonate by montmorillonite.

    PubMed

    Yang, Kun; Zhu, Lizhong; Xing, Baoshan

    2007-01-01

    Sorption of linear alkylbenzene sulfonates by soils and sediments is an important process that may affect their fate, transport, toxicity and their application in remediation of contaminated soil and groundwater. In this study, batch experiments were conducted to elucidate the sorption of a widely used anionic surfactant, sodium dodecylbenzene sulfonate (SDBS), by montmorillonite. It was observed that: (i) SDBS was sorbed significantly by montmorillonite saturated with Ca(2+), but little by Na-saturated montmorillonite; (ii) the amount of SDBS sorbed by Ca(2+)-montmorillonite was enhanced by NaCl; and (iii) no significant intercalation of SDBS into Ca(2+)-montmorillonite was observed by X-ray diffraction (XRD) analysis. These results indicate that the removal of SDBS by Ca(2+)-montmorillonite was primarily attributed to the precipitation between DBS(-) and Ca(2+) in solution which was released from montmorillonite via cation exchange. These results will help us to understand the sorption behavior and environmental effects of anionic surfactants.

  20. Phase behavior of simple salt tolerant sulfonates

    SciTech Connect

    Barakat, Y.; Fortney, L.N.; Lalanne-Cassou, C.; Schechter, R.S.; Wade, W.H.; Yiv, S.H.

    1982-01-01

    Alkane and /alpha/-olefin sulfonates can be utilized to produce optimal microemulsion formulations which have very high salinity (including divalent ion) tolerance while maintaining large solubilization parameters and low interfacial tensions. Such molecules require elevated temperatures or higher alcohol concentrations to suppress liquid crystal formulation. As found for other species, solubilization is inversely related to width of the three phase regime, and interfacial tension and solubilization are strongly coupled. 18 refs.

  1. Phase behavior of simple salt tolerant sulfonates

    SciTech Connect

    Barakat, Y.; Fortney, L.N.; Lalanne-Cassou, C.; Schechter, R.S.; Wade, W.H.; Yiv, S.H.

    1982-01-01

    Alkane and ..cap alpha..-olefin sulfonates can be utilized to produce optimal microemulsion formulations which have very high salinity (including divalent ion) tolerance while maintaining large solubilization parameters and low interfacial tensions. Such molecules require elevated temperatures or higher alcohol concentrations to suppress liquid crystal formation. As found for other species, solubilization is inversely related to width of the three phase regime, and interfacial tension and solubilization are strongly coupled.

  2. High Lipophilicty of Perfluoroalkyl Carboxylate and Sulfonate

    PubMed Central

    Jing, Ping; Rodgers, Patrick J.; Amemiya, Shigeru

    2009-01-01

    Here we report on remarkably high lipophilicity of perfluoroalkyl carboxylate and sulfonate. A lipophilic nature of this emerging class of organic pollutants has been hypothesized as an origin of their bioaccumulation and toxicity. Both carboxylate and sulfonate, however, are considered hydrophilic while perfluroalkyl groups are not only hydrophobic but also oleophobic. Partition coefficients of homologous series of perfluoroalkyl and alkyl carboxylates between water and n-octanol were determined as a measure of their lipophilicity by ion-transfer cyclic voltammetry. Very similar lipophilicity of perfluoroalkyl and alkyl chains with the same length is demonstrated experimentally for the first time by fragment analysis of the partition coefficients. This finding is important for pharmaceutical and biomedical applications of perfluoroalkyl compounds. Interestingly, ∼2 orders of magnitude higher lipophilicity of a perfluoroalkyl carboxylate or sulfonate in comparison to its alkyl counterpart is ascribed nearly exclusively to their oxoanion groups. The higher lipophilicity originates from a strong electron-withdrawing effect of the perfluoroalkyl group on the adjacent oxoanion group, which is weakly hydrated to decrease its hydrophilicity. In fact, the inductive effect is dramatically reduced for a fluorotelomer with an ethylene spacer between perfluorohexyl and carboxylate groups, which is only as lipophilic as its alkyl counterpart, nonanoate, and is 400 times less lipophilic than perfluorononanoate. The high lipophilicity of perfluoroalkyl carboxylate and sulfonate implies that their permeation across such a thin lipophilic membrane as a bilayer lipid membrane is limited by their transfer at a membrane/water interface. The limiting permeability is lower and less dependent on their lipophilicity than the permeability controlled by their diffusion in the membrane interior as assumed in the classical solubility-diffusion model. PMID:19170492

  3. Preparation of Chitosan/Polystyrene Sulfonate Multilayered Composite Metal Nanoparticles and Its Application.

    PubMed

    Xiong, Fangxin; Chen, Chunxiao; Liu, Shantang

    2016-06-01

    Metal-Chitosan (CTS) composite was first synthesized through the metal composition of chitosan (CTS) and metal ions. The formed composite was alternately deposited on the base with sodium polystyrene sulfonate (PSS) through a layer-by-layer self-assembling technique, followed by an in situ reduction by sodium borohydride to produce a polyelectrolyte nanocomposite thin film containing metal nanoparticles. Assembly, surface morphology and electrochemical properties of the composite membrane were analyzed by UV-visible absorption spectroscopy (UV-vis), atomic force microscopy (AFM) and cyclic voltammetry (CV). The UV-Vis results indicated that the absorbance of the multilayer film at the characteristic absorption peak increased as the membrane bilayers increased, in a good linear relationship, which demonstrated that the multilayer film was uniformly assembled on the base. AFM images showed that the surface of the multilayer thin-film composite had some degree of roughness and metal nanoparticles of 10-20 nm in size were generated on the membrane. The CV results indicated that the metal nanocomposite film had excellent electrocatalytic activity to glucose and had a potential for applications in electrochemical sensors.

  4. Preparation of Chitosan/Polystyrene Sulfonate Multilayered Composite Metal Nanoparticles and Its Application.

    PubMed

    Xiong, Fangxin; Chen, Chunxiao; Liu, Shantang

    2016-06-01

    Metal-Chitosan (CTS) composite was first synthesized through the metal composition of chitosan (CTS) and metal ions. The formed composite was alternately deposited on the base with sodium polystyrene sulfonate (PSS) through a layer-by-layer self-assembling technique, followed by an in situ reduction by sodium borohydride to produce a polyelectrolyte nanocomposite thin film containing metal nanoparticles. Assembly, surface morphology and electrochemical properties of the composite membrane were analyzed by UV-visible absorption spectroscopy (UV-vis), atomic force microscopy (AFM) and cyclic voltammetry (CV). The UV-Vis results indicated that the absorbance of the multilayer film at the characteristic absorption peak increased as the membrane bilayers increased, in a good linear relationship, which demonstrated that the multilayer film was uniformly assembled on the base. AFM images showed that the surface of the multilayer thin-film composite had some degree of roughness and metal nanoparticles of 10-20 nm in size were generated on the membrane. The CV results indicated that the metal nanocomposite film had excellent electrocatalytic activity to glucose and had a potential for applications in electrochemical sensors. PMID:27427666

  5. Exciton quenching at PEDOT:PSS anode in polymer blue-light-emitting diodes

    SciTech Connect

    Abbaszadeh, D.; Wetzelaer, G. A. H.; Nicolai, H. T.

    2014-12-14

    The quenching of excitons at the poly(3,4-ethylenedioxythiophene):poly(styrenesulfonic acid) (PEDOT:PSS) anode in blue polyalkoxyspirobifluorene-arylamine polymer light-emitting diodes is investigated. Due to the combination of a higher electron mobility and the presence of electron traps, the recombination zone shifts from the cathode to the anode with increasing voltage. The exciton quenching at the anode at higher voltages leads to an efficiency roll-off. The voltage dependence of the luminous efficiency is reproduced by a drift-diffusion model under the condition that quenching of excitons at the PEDOT:PSS anode and metallic cathode is of equal strength. Experimentally, the efficiency roll-off at high voltages due to anode quenching is eliminated by the use of an electron-blocking layer between the anode and the light-emitting polymer.

  6. PEDOT:PSS/GO nanocomposites: Determination of the aspect ratio by indirect measurements

    NASA Astrophysics Data System (ADS)

    Giuri, Antonella; Colella, Silvia; Listorti, Andrea; Rizzo, Aurora; Corcione, Carola Esposito

    2016-05-01

    Polymer nanocomposites properties significantly depend on the average size of the fillers dispersed into the matrix and on the grade of the dispersion, the latter influenced by the process techniques. In this work, we determined the aspect ratio of graphene oxide (GO) dispersed into Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS), starting from the indirect measurement of the rheological behavior of polymer/filler mixtures, as a function of the shear rate and the volumetric composition. PEDOT:PSS+GO nanocomposite films were also realized by spin coating on different substrates and characterized by Scanning electron microscopy (SEM) and X-ray diffraction (XRD), in order to analyze the quality of the dispersion, even by direct measurements.

  7. A synthetic approach for enhanced thermoelectric properties of PEDOT:PSS bulk composites

    NASA Astrophysics Data System (ADS)

    Wei, Kaya; Stedman, Troy; Ge, Zhen-Hua; Woods, Lilia M.; Nolas, George S.

    2015-10-01

    The thermoelectric properties of PEDOT:PSS/Bi0.5Sb1.5Te3 polymer/inorganic bulk composites with different Bi0.5Sb1.5Te3 content were investigated. The composites were prepared at various concentrations of Bi0.5Sb1.5Te3 by a solution-phase process before grinding to fine powders in liquid N2 for hot pressing into bulk polymer composite materials. The measured transport properties are well described within a theoretical model for effective media involving a tunneling mechanism induced by thermal voltage fluctuations. Our results present a strategy for the preparation of bulk polymer composites and demonstrate an avenue for optimization of the thermoelectric properties of PEDOT:PSS/Bi0.5Sb1.5Te3 bulk composites.

  8. Planar silver nanowire, carbon nanotube and PEDOT:PSS nanocomposite transparent electrodes

    NASA Astrophysics Data System (ADS)

    Stapleton, Andrew J.; Yambem, Soniya D.; Johns, Ashley H.; Afre, Rakesh A.; Ellis, Amanda V.; Shapter, Joe G.; Andersson, Gunther G.; Quinton, Jamie S.; Burn, Paul L.; Meredith, Paul; Lewis, David A.

    2015-04-01

    Highly conductive, transparent and flexible planar electrodes were fabricated using interwoven silver nanowires and single-walled carbon nanotubes (AgNW:SWCNT) in a PEDOT:PSS matrix via an epoxy transfer method from a silicon template. The planar electrodes achieved a sheet resistance of 6.6 ± 0.0 Ω/□ and an average transmission of 86% between 400 and 800 nm. A high figure of merit of 367 Ω-1 is reported for the electrodes, which is much higher than that measured for indium tin oxide and reported for other AgNW composites. The AgNW:SWCNT:PEDOT:PSS electrode was used to fabricate low temperature (annealing free) devices demonstrating their potential to function with a range of organic semiconducting polymer:fullerene bulk heterojunction blend systems.

  9. P-doped organic semiconductor: Potential replacement for PEDOT:PSS in organic photodetectors

    NASA Astrophysics Data System (ADS)

    Herrbach, J.; Revaux, A.; Vuillaume, D.; Kahn, A.

    2016-08-01

    In this work, we present an alternative to the use of PEDOT:PSS as hole transport and electron blocking layers in organic photodetectors processed by solution. As Poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) is known to be sensitive to humidity, oxygen, and UV, removing this layer is essential for lifetime improvements. As a first step to achieving this goal, we need to find an alternative layer that fulfills the same role in order to obtain a working diode with similar or better performance. As a replacement, a layer of poly[(4,8-bis-(2-ethylhexyloxy)-benzo(1,2-b:4,5-b')dithiophene)-2,6-diyl-alt-(4-(2-ethylhexanoyl)-thieno[3,4-b]thiophene-)-2-6-diyl)] (PBDTTT-c) p-doped with the dopant tris-[1-(trifluoroethanoyl)-2-(trifluoromethyl)ethane-1,2-dithiolene] (Mo(tfd-COCF3)3) is used. This p-doped layer effectively lowers the hole injection barrier, and the low electron affinity of the polymer prevents the injection of electrons into the active layer. We show similar device performance under light and the improvements of detection performance with the doped layer in comparison with PEDOT:PSS, leading to a detectivity of 1.9 × 1013 cm (Hz)1/2 (W)-1, competitive with silicon diodes used in imaging applications. Moreover, contrary to PEDOT:PSS, no localization of the p-doped layer is needed, leading to a diode active area defined by the patterned electrodes.

  10. Electrodeposition and characterisation of polypyrroles containing sulfonated carbon nanotubes.

    PubMed

    Lynam, Carol; Wallace, Gordon G; Officer, David L

    2007-10-01

    Using facile diazonium chemistry, sulfonate groups have been covalently attached to single wall carbon nanotubes. The resulting sulfonated tubes form a stable aqueous dispersion in the presence of pyrrole monomer. Subsequent electropolymerisation results in a conductive, electroactive polypyrrole doped with sulfonated tubes being formed at unusually low potentials. The potential of this material as a host matrix for biomolecules has been demonstrated by entrapping horse-radish peroxidase directly in the polypyrrole during composite formation.

  11. Selective detection of dopamine with an all PEDOT:PSS Organic Electrochemical Transistor

    PubMed Central

    Gualandi, Isacco; Tonelli, Domenica; Mariani, Federica; Scavetta, Erika; Marzocchi, Marco; Fraboni, Beatrice

    2016-01-01

    An all PEDOT:PSS Organic Electrochemical Transistor (OECT) has been developed and used for the selective detection of dopamine (DA) in the presence of interfering compounds (ascorbic acid, AA and uric acid, UA). The selective response has been implemented using a potentiodynamic approach, by varying the operating gate voltage and the scan rate. The trans-conductance curves allow to obtain a linear calibration plot for AA, UA and DA and to separate the redox waves associated to each compound; for this purpose, the scan rate is an important parameter to achieve a good resolution. The sensitivities and limits of detection obtained with the OECT have been compared with those obtained by potential step amperometric techniques (cyclic voltammetry and differential pulse voltammetry), employing a PEDOT:PSS working electrode: our results prove that the all-PEDOT:PSS OECT sensitivities and limits of detection are comparable or even better than those obtained by DPV, a technique that employs a sophisticate potential wave and read-out system in order to maximize the performance of electrochemical sensors and that can hardly be considered a viable readout method in practical applications. PMID:27739467

  12. Growth Mechanism of Strain-Dependent Morphological Change in PEDOT:PSS Films

    PubMed Central

    Lee, Yoo-Yong; Choi, Gwang Mook; Lim, Seung-Min; Cho, Ju-Young; Choi, In-Suk; Nam, Ki Tae; Joo, Young-Chang

    2016-01-01

    Understanding the mechanism of the strain-dependent conductivity change in polymers in stretched conditions is important. We observed a strain-induced growth of the conductive regions of PEDOT:PSS films, induced by a coalescence of conductive PEDOT-rich cores. This growth due to coalescence leads to a gradual decrease in the electrical resistivity up to 95%, independent of the thickness of the PEDOT:PSS films. The primary mechanism for the evolution of the PEDOT-rich cores proceeds by the cores growing larger as they consuming relatively smaller cores. This process is caused by a strain-induced local rearrangement of PEDOT segments in the vicinity of PSS shells around the cores and also changes the chemical environment in PEDOT, induced by the electron-withdrawing effects around the PEDOT chains. The strain-induced growth mechanism is beneficial to understanding the phenomenon of polymeric chain rearrangement in mechanical deformation and to modulating the electrical conductivity for practical applications. PMID:27125340

  13. Effect of incorporation of ethylene glycol into PEDOT:PSS on electron phonon coupling and conductivity

    SciTech Connect

    Lin, Yow-Jon Ni, Wei-Shih; Lee, Jhe-You

    2015-06-07

    The effect of incorporation of ethylene glycol (EG) into poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) on electron phonon coupling and conductivity is investigated. It is shown that the carrier density (N{sub C}) increases significantly and the carrier mobility (μ) increases slightly at 300 K. The increased intensity of the Raman spectrum between 1400 and 1450 cm{sup −1}, following EG treatment (that is, the quinoid-dominated structures of the PEDOT chain), leads to an increase in the number of polarons (bipolarons), which leads to an increase in N{sub C}. In addition, μ in PEDOT:PSS samples with or without EG addition exhibits a strong temperature dependence, which demonstrates the dominance of tunneling (hopping) at low (high) temperatures. The high conductivity of PEDOT:PSS samples with the addition of EG is attributed to the combined effect of the modification of the electron-phonon coupling and the increase in N{sub C} (μ)

  14. Anticoagulant and antithrombotic activities of low-molecular-weight propylene glycol alginate sodium sulfate (PSS).

    PubMed

    Xin, Meng; Ren, Li; Sun, Yang; Li, Hai-hua; Guan, Hua-Shi; He, Xiao-Xi; Li, Chun-Xia

    2016-05-23

    Propylene glycol alginate sodium sulfate (PSS), a sulfated polysaccharide derivative, has been used as a heparinoid drug to prevent and treat hyperlipidemia and ischemic cardio-cerebrovascular diseases in China for nearly 30 years. To extend the applications of PSS, a series of low-molecular-weight PSSs (named FPs) were prepared by oxidative-reductive depolymerization, and the antithrombotic activities were investigated thoroughly in vitro and in vivo. The bioactivity evaluation demonstrated a positive correlation between the molecular weight and the anticoagulant and antithrombotic activities of FPs. FPs could prolong the APTT and clotting time and reduce platelet aggregation significantly. FPs could also effectively inhibit factor IIa in the presence of AT-III and HC-II. FPs decreased the wet weights and lengths of the thrombus and increased occlusion times in vivo. FP-6k, a PSS fragment with a molecular weight of 6 kDa, is an optimal antithrombotic candidate for further study and showed little chance for hemorrhagic action.

  15. PEDOT:PSS emitters on multicrystalline silicon thin-film absorbers for hybrid solar cells

    SciTech Connect

    Junghanns, Marcus; Plentz, Jonathan Andrä, Gudrun; Gawlik, Annett; Höger, Ingmar; Falk, Fritz

    2015-02-23

    We fabricated an efficient hybrid solar cell by spin coating poly(3,4-ethylene-dioxythiophene):polystyrenesulfonate (PEDOT:PSS) on planar multicrystalline Si (mc-Si) thin films. The only 5 μm thin Si absorber layers were prepared by diode laser crystallization of amorphous Si deposited by electron beam evaporation on glass. On these absorber layers, we studied the effect of SiO{sub x} and Al{sub 2}O{sub 3} terminated Si surfaces. The short circuit density and power conversion efficiency (PCE) of the mc-Si/Al{sub 2}O{sub 3}/PEDOT:PSS solar cell increase from 20.6 to 25.4 mA/cm{sup 2} and from 7.3% to 10.3%, respectively, as compared to the mc-Si/SiO{sub x}/PEDOT:PSS cell. Al{sub 2}O{sub 3} lowers the interface recombination and improves the adhesion of the polymer film on the hydrophobic mc-Si thin film. Open circuit voltages up to 604 mV were reached. This study demonstrates the highest PCE so far of a hybrid solar cell with a planar thin film Si absorber.

  16. Si/PEDOT:PSS Hybrid Solar Cells with Advanced Antireflection and Back Surface Field Designs

    NASA Astrophysics Data System (ADS)

    Sun, Yiling; Yang, Zhenhai; Gao, Pingqi; He, Jian; Yang, Xi; Sheng, Jiang; Wu, Sudong; Xiang, Yong; Ye, Jichun

    2016-08-01

    Molybdenum oxide (MoO3) is one of most suitable antireflection (AR) layers for silicon/poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (Si/PEDOT:PSS) hybrid solar cells due to its well-matched refractive index (2.1). A simulation model was employed to predict the optical characteristics of Si/PEDOT:PSS hybrid solar cells with the MoO3 layers as antireflection coatings (ARCs), as well as to analyze the loss in current density. By adding an optimum thickness of a 34-nm-thick ARC of MoO3 on the front side and an effective rear back surface field (BSF) of phosphorus-diffused N + layer at the rear side, the hybrid cells displayed higher light response in the visible and near infrared regions, boosting a short-circuit current density ( J sc) up to 28.7 mA/cm2. The average power conversion efficiency (PCE) of the Si/PEDOT:PSS hybrid solar cells was thus increased up to 11.90 %, greater than the value of 9.23 % for the reference devices.

  17. Improved PEDOT:PSS/c-Si hybrid solar cell using inverted structure and effective passivation

    NASA Astrophysics Data System (ADS)

    Zhang, Xisheng; Yang, Dong; Yang, Zhou; Guo, Xiaojia; Liu, Bin; Ren, Xiaodong; Liu, Shengzhong (Frank)

    2016-10-01

    The PEDOT:PSS is often used as the window layer in the normal structured PEDOT:PSS/c-Si hybrid solar cell (HSC), leading to significantly reduced response, especially in red and near-infrared region. By depositing the PEDOT:PSS on the rear side of the c-Si wafer, we developed an inverted structured HSC with much higher solar cell response in the red and near-infrared spectrum. Passivating the other side with hydrogenated amorphous silicon (a-Si:H) before electrode deposition, the minority carrier lifetime has been significantly increased and the power conversion efficiency (PCE) of the inverted HSC is improved to as high as 16.1% with an open-circuit voltage (Voc) of 634 mV, fill factor (FF) of 70.5%, and short-circuit current density (Jsc) of 36.2 mA cm‑2, an improvement of 33% over the control device. The improvements are ascribed to inverted configuration and a-Si:H passivation, which can increase photon carrier generation and reduce carrier recombination, respectively. Both of them will benefit the photovoltaic performance and should be considered as effective design strategies to improve the performance of organic/c-Si HSCs.

  18. Electrical transport characterization of benzenedithiol and methylbenzenethiol molecular junctions with PEDOT:PSS interlayer electrodes

    NASA Astrophysics Data System (ADS)

    Jeong, Inho; Song, Hyunwook

    2016-08-01

    We have fabricated and characterized molecular electronic devices using benzene-based molecular monolayers and PEDOT:PSS (3,4-ethylenedioxythiophene) interlayer electrodes. In particular, we compared the electrical characteristics of two different benzenethiol molecules, 4-methylbenzenethiol (MBT) and 1,4-benzenedithiol (BDT), which have the same backbone structure but different top-end groups. From statistically representative data, we observed that the current density of the MBT devices was greater than that of the BDT devices by a factor of ˜4. The difference in current density between the two molecular electronic devices was attributed to the difference in the contact properties between the MBT and BDT molecules with the PEDOT:PSS interlayer electrodes. We also found an increase in the current density with increasing temperature within the range of 300 - 400 K, which could be caused by changes in the interfacial properties of the PEDOT:PSS-molecule contact and by removal of residual solvent or water from the interface.

  19. Growth Mechanism of Strain-Dependent Morphological Change in PEDOT:PSS Films

    NASA Astrophysics Data System (ADS)

    Lee, Yoo-Yong; Choi, Gwang Mook; Lim, Seung-Min; Cho, Ju-Young; Choi, In-Suk; Nam, Ki Tae; Joo, Young-Chang

    2016-04-01

    Understanding the mechanism of the strain-dependent conductivity change in polymers in stretched conditions is important. We observed a strain-induced growth of the conductive regions of PEDOT:PSS films, induced by a coalescence of conductive PEDOT-rich cores. This growth due to coalescence leads to a gradual decrease in the electrical resistivity up to 95%, independent of the thickness of the PEDOT:PSS films. The primary mechanism for the evolution of the PEDOT-rich cores proceeds by the cores growing larger as they consuming relatively smaller cores. This process is caused by a strain-induced local rearrangement of PEDOT segments in the vicinity of PSS shells around the cores and also changes the chemical environment in PEDOT, induced by the electron-withdrawing effects around the PEDOT chains. The strain-induced growth mechanism is beneficial to understanding the phenomenon of polymeric chain rearrangement in mechanical deformation and to modulating the electrical conductivity for practical applications.

  20. Improved PEDOT:PSS/c-Si hybrid solar cell using inverted structure and effective passivation

    PubMed Central

    Zhang, Xisheng; Yang, Dong; Yang, Zhou; Guo, Xiaojia; Liu, Bin; Ren, Xiaodong; Liu, Shengzhong (Frank)

    2016-01-01

    The PEDOT:PSS is often used as the window layer in the normal structured PEDOT:PSS/c-Si hybrid solar cell (HSC), leading to significantly reduced response, especially in red and near-infrared region. By depositing the PEDOT:PSS on the rear side of the c-Si wafer, we developed an inverted structured HSC with much higher solar cell response in the red and near-infrared spectrum. Passivating the other side with hydrogenated amorphous silicon (a-Si:H) before electrode deposition, the minority carrier lifetime has been significantly increased and the power conversion efficiency (PCE) of the inverted HSC is improved to as high as 16.1% with an open-circuit voltage (Voc) of 634 mV, fill factor (FF) of 70.5%, and short-circuit current density (Jsc) of 36.2 mA cm−2, an improvement of 33% over the control device. The improvements are ascribed to inverted configuration and a-Si:H passivation, which can increase photon carrier generation and reduce carrier recombination, respectively. Both of them will benefit the photovoltaic performance and should be considered as effective design strategies to improve the performance of organic/c-Si HSCs. PMID:27725714

  1. Selective detection of dopamine with an all PEDOT:PSS Organic Electrochemical Transistor

    NASA Astrophysics Data System (ADS)

    Gualandi, Isacco; Tonelli, Domenica; Mariani, Federica; Scavetta, Erika; Marzocchi, Marco; Fraboni, Beatrice

    2016-10-01

    An all PEDOT:PSS Organic Electrochemical Transistor (OECT) has been developed and used for the selective detection of dopamine (DA) in the presence of interfering compounds (ascorbic acid, AA and uric acid, UA). The selective response has been implemented using a potentiodynamic approach, by varying the operating gate voltage and the scan rate. The trans-conductance curves allow to obtain a linear calibration plot for AA, UA and DA and to separate the redox waves associated to each compound; for this purpose, the scan rate is an important parameter to achieve a good resolution. The sensitivities and limits of detection obtained with the OECT have been compared with those obtained by potential step amperometric techniques (cyclic voltammetry and differential pulse voltammetry), employing a PEDOT:PSS working electrode: our results prove that the all-PEDOT:PSS OECT sensitivities and limits of detection are comparable or even better than those obtained by DPV, a technique that employs a sophisticate potential wave and read-out system in order to maximize the performance of electrochemical sensors and that can hardly be considered a viable readout method in practical applications.

  2. Anticoagulant and antithrombotic activities of low-molecular-weight propylene glycol alginate sodium sulfate (PSS).

    PubMed

    Xin, Meng; Ren, Li; Sun, Yang; Li, Hai-hua; Guan, Hua-Shi; He, Xiao-Xi; Li, Chun-Xia

    2016-05-23

    Propylene glycol alginate sodium sulfate (PSS), a sulfated polysaccharide derivative, has been used as a heparinoid drug to prevent and treat hyperlipidemia and ischemic cardio-cerebrovascular diseases in China for nearly 30 years. To extend the applications of PSS, a series of low-molecular-weight PSSs (named FPs) were prepared by oxidative-reductive depolymerization, and the antithrombotic activities were investigated thoroughly in vitro and in vivo. The bioactivity evaluation demonstrated a positive correlation between the molecular weight and the anticoagulant and antithrombotic activities of FPs. FPs could prolong the APTT and clotting time and reduce platelet aggregation significantly. FPs could also effectively inhibit factor IIa in the presence of AT-III and HC-II. FPs decreased the wet weights and lengths of the thrombus and increased occlusion times in vivo. FP-6k, a PSS fragment with a molecular weight of 6 kDa, is an optimal antithrombotic candidate for further study and showed little chance for hemorrhagic action. PMID:26974373

  3. Effect of low energy ion irradiation on the transport and structural behavior of PEDOT:PSS systems

    NASA Astrophysics Data System (ADS)

    Shilpa, S.; Venkatachalaiah, K. N.; Damle, R.; Kumar, Pravin; Kanjilal, D.; Kumaraswamy, G. N.

    2016-05-01

    In the past two decades, organic conductors have been widely explored for use in different applications. One of the extensively studied organic material for the use in the field of electronic devices is PEDOT:PSS. Organic/inorganic nanocomposite systems have been developed to improve the properties of organic materials. In the present study, we have made an attempt to understand the effect of low energy oxygen ion beam irradiation on the electrical and structural properties of PEDOT:PSS and PEDOT:PSS/TiO2 nanocomposites. The observed reduction in electrical properties in PEDOT:PSS systems may be linked to radiation induced phase change. The nanocomposite systems show better stability to the ion irradiation compared to the pure systems.

  4. Efficacy of Heparinoid PSS in Treating Cardiovascular Diseases and Beyond-A Review of 27 Years Clinical Experiences in China.

    PubMed

    Zeng, Yangyang; Yang, Desheng; Qiu, Peiju; Han, Zhangrun; Zeng, Pengjiao; He, Yanli; Guo, Zhihua; Xu, Lingling; Cui, Yidi; Zhou, Zijing; Zhang, Meng; Hao, Jiejie; Zhang, Lijuan

    2016-04-01

    Propylene glycol alginate sodium sulfate (PSS) is the world's first oral heparinoid approved by Chinese Food and Drug Administration in 1987. Propylene glycol alginate sodium sulfate is produced by modifying partially hydrolyzed alginate, one of the most abundant marine polysaccharides isolated from brown algae, by epoxypropane esterification and by chemical sulfation. It is used for treating and preventing cardiovascular-related diseases. The low cost (US$1.29/100 tablets, ∼4 tablets/day), remarkable clinical effects, and convenient oral administration make PSS an ideal long-term prevention drug. Propylene glycol alginate sodium sulfate is available in most drug stores in China, and millions of patients take PSS routinely during the past 27 years. The 22 784 reported clinical cases as well as the structure, preparation, clinical efficacy, adverse reactions, pharmacokinetics, pharmacodynamics, and future perspectives of PSS based on the results of peer-reviewed publications will be discussed. This review should bring the knowledge of PSS gained in China to the world to stimulate in depth academic and clinical studies of PSS.

  5. Sulfonimide-containing poly(arylene ether)s and poly(arylene ether sulfone)s, methods for producing the same, and uses thereof

    DOEpatents

    Hofmann, Michael A.

    2006-11-14

    The present invention is directed to sulfonimide-containing polymers, specifically sulfonimide-containing poly(arylene ether)s and sulfonimide-containing poly(arylene ether sulfone)s, and processes for making the sulfonimide-containing poly(arylene ether)s and sulfonimide-containing poly(arylene ether sulfone)s, for use conductive membranes and fuel cells.

  6. Acid-mediated formation of trifluoromethyl sulfonates from sulfonic acids and a hypervalent iodine trifluoromethylating agent.

    PubMed

    Koller, Raffael; Huchet, Quentin; Battaglia, Philip; Welch, Jan M; Togni, Antonio

    2009-10-28

    A variety of sulfonic acids have been trifluoromethylated using 1-trifluoromethyl-1,2-benziodoxol-3(1H)-one under mild conditions in good to excellent yields. Initial mechanistic investigations of this reaction show a clean second-order kinetics and only very weak substrate electronic effects.

  7. Molecular sieve/sulfonated poly(ether ketone ether sulfone) composite membrane as proton exchange membrane

    NASA Astrophysics Data System (ADS)

    Changkhamchom, Sairung; Sirivat, Anuvat

    2012-02-01

    A proton exchange membrane (PEM) is an electrolyte membrane used in both polymer electrolyte membrane fuel cells (PEMFC) and direct methanol fuel cells (DMFCs). Currently, PEMs typically used for PEMFCs are mainly the commercially available Nafion^ membranes, which is high cost and loss of proton conductivity at elevated temperature. In this work, the Sulfonated poly(ether ketone ether sulfone), (S-PEKES), was synthesized by the nucleophilic aromatic substitution polycondensation between bisphenol S and 4,4'-dichlorobenzophenone, and followed by the sulfonation reaction with concentrated sulfuric acid. The molecular sieve was added in the S-PEKES matrix at various ratios to form composite membranes to be the candidate for PEM. Properties of both pure sulfonated polymer and composite membranes were compared with the commercial Nafion^ 117 membrane from Dupont. S-PEKES membranes cast from these materials were evaluated as a polymer electrolyte membrane for direct methanol fuel cells. The main properties investigated were the proton conductivity, methanol permeability, thermal, chemical, oxidative, and mechanical stabilities by using a LCR meter, Gas Chromatography, Thermogravimetric Analysis, Fourier Transform Infrared Spectroscopy, Fenton's reagent, and Universal Testing Machine. The addition of the molecular sieve helped to increase both the proton conductivity and the methanol stability. These composite membranes are shown as to be potential candidates for use as a Proton Exchange Membrane (PEM).

  8. Boiling significantly promotes photodegradation of perfluorooctane sulfonate.

    PubMed

    Lyu, Xian-Jin; Li, Wen-Wei; Lam, Paul K S; Yu, Han-Qing

    2015-11-01

    The application of photochemical processes for perfluorooctane sulfonate (PFOS) degradation has been limited by a low treatment efficiency. This study reports a significant acceleration of PFOS photodegradation under boiling condition compared with the non-boiling control. The PFOS decomposition rate increased with the increasing boiling intensity, but declined at a higher hydronium level or under oxygenation. These results suggest that the boiling state of solution resulted in higher effective concentrations of reactants at the gas-liquid interface and enhanced the interfacial mass transfer, thereby accelerating the PFOS decomposition. This study broadens our knowledge of PFOS photodegradation process and may have implications for development of efficient photodegradation technologies. PMID:26117498

  9. Boiling significantly promotes photodegradation of perfluorooctane sulfonate.

    PubMed

    Lyu, Xian-Jin; Li, Wen-Wei; Lam, Paul K S; Yu, Han-Qing

    2015-11-01

    The application of photochemical processes for perfluorooctane sulfonate (PFOS) degradation has been limited by a low treatment efficiency. This study reports a significant acceleration of PFOS photodegradation under boiling condition compared with the non-boiling control. The PFOS decomposition rate increased with the increasing boiling intensity, but declined at a higher hydronium level or under oxygenation. These results suggest that the boiling state of solution resulted in higher effective concentrations of reactants at the gas-liquid interface and enhanced the interfacial mass transfer, thereby accelerating the PFOS decomposition. This study broadens our knowledge of PFOS photodegradation process and may have implications for development of efficient photodegradation technologies.

  10. Interaction between amphiphilic ionic liquid 1-butyl-3-methylimidazolium octyl sulfate and anionic polymer of sodium polystyrene sulfonate in aqueous medium

    NASA Astrophysics Data System (ADS)

    Barhoumi, Z.; Saini, M.; Amdouni, N.; Pal, A.

    2016-09-01

    The micellization of an aqueous solution of the surface active ionic liquid (SAIL), 1-butyl-3-methylimidazolium octylsufate (C4mim)(C8OSO3) and its interaction with an anionic polymer sodium polystyrene sulfonate, (NaPSS) were studied using conductimetry, tensiometry and fluorimetry. Surface tension profile shows a more dramatic increase in the value of surface tension of aqueous (C4mim)(C8OSO3) before the critical micelle concentration (cmc) of IL. The critical micelle concentration (cmc) value of this surfactant was found out from conductance measurements. The thermodynamic parameters, i.e., Gibb's free energy, enthalpy, and entropy of micellization of the IL in aqueous solution have been calculated. Behavior of fluorescence probe confirms the binding interactions between SAIL and the polyelectrolyte.

  11. Synthesis of cyclic sulfones by ring-closing metathesis.

    PubMed

    Yao, Qingwei

    2002-02-01

    A general and highly efficient synthesis of cyclic sulfones based on ring-closing metathesis has been developed. The synthetic utility of the resulting cyclic sulfones was demonstrated by their participation in stereoselective Diels-Alder reactions and transformation to cyclic dienes by the Ramberg-Bäcklund reaction. PMID:11820896

  12. Synthesis of basic and overbasic sulfonate detergent additives

    SciTech Connect

    Abou El Naga, H.H.; Abd El-Azim, W.M.; Bendary, S.A.; Awad, N.G.

    1993-12-01

    Heavy alkylbenzene, which accumulates as a by-product from linear alkylbenzene synthesis, is evaluated as a starting material for preparation of basic and over basic sulfonate detergent additives. Chemical structure analysis showed that this by-product contains several components in different proportions. Most of these components, as traced via mass spectrometry, showed the presence of paraffinic side chains within the carbon range C{sub 11}--C{sub 22}. Accordingly, sulfonation conditions for it were adjusted to optimize the reaction yield and sulfonic quality. Neutralization of the sulfonic acid was carried out by adding CaO in the presence of methanol as a promoter. Preparation of over basic sulfonate was run via a carbonation process at 55--60 C. Evaluations of synthesized basic calcium sulfonate in comparison to a commercial additive is supported by its efficiency as a detergent additive. The synthesized product has a higher total base number and Ca content than those for the commercial one. On the other hand, evaluation of the synthesized overbasic calcium sulfonate compared with overbasic commercial additives with medium and high alkalinity indicated that the synthesized product can be classified as overbasic calcium sulfonate with medium alkalinity, good dispersive power, and detergent efficiency.

  13. 21 CFR 177.2210 - Ethylene polymer, chloro-sulfonated.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Ethylene polymer, chloro-sulfonated. 177.2210... (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use Only as Components of Articles Intended for Repeated Use § 177.2210 Ethylene polymer, chloro-sulfonated. Ethylene polymer, chlorosulfonated...

  14. Sulfonated Nanoplates in Proton Conducting Membranes for Fuel Cells

    SciTech Connect

    Chen, W.F.; Ni’mah, H.; Yu-Cheng Shen, Y.-C.; Kuo, P.-L.

    2011-09-29

    Surface-functionalized nanoplates are synthesized by anchoring sulfonic acid containing siloxanes on zirconium phosphate, and in turn blended with Nafion to fabricate proton conducting membranes. The effects of these sulfonated nanoplates on proton conduction, hydro-characteristics and fuel cell performance are reported.

  15. Synthesis of cyclic sulfones by ring-closing metathesis.

    PubMed

    Yao, Qingwei

    2002-02-01

    A general and highly efficient synthesis of cyclic sulfones based on ring-closing metathesis has been developed. The synthetic utility of the resulting cyclic sulfones was demonstrated by their participation in stereoselective Diels-Alder reactions and transformation to cyclic dienes by the Ramberg-Bäcklund reaction.

  16. MATERNAL AND DEVELOPMENTAL TOXICITY OF PERFLUOROOCTANE SULFONATE IN THE RAT

    EPA Science Inventory

    MATERNAL AND DEVELOPMENTAL TOXICITY OF PERFLUOROOCTANE SULFONATE IN THE RAT.
    C. Lau and J.M. Rogers, Reproductive Toxicology Division, NHEERL, ORD, USEPA, Research Triangle Park, NC, USA

    Perfluorooctane sulfonate (PFOS), an environmentally persistent compound used ...

  17. 40 CFR 721.1625 - Alkylbenzene sulfonate, amine salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Alkylbenzene sulfonate, amine salt... Substances § 721.1625 Alkylbenzene sulfonate, amine salt. (a) Chemical substance and significant new uses... salt (PMN P-90-456) is subject to reporting under this section for the significant new use described...

  18. 40 CFR 721.1625 - Alkylbenzene sulfonate, amine salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Alkylbenzene sulfonate, amine salt... Substances § 721.1625 Alkylbenzene sulfonate, amine salt. (a) Chemical substance and significant new uses... salt (PMN P-90-456) is subject to reporting under this section for the significant new use described...

  19. Anaerobic degradation of linear alkylbenzene sulfonate.

    PubMed

    Mogensen, Anders S; Haagensen, Frank; Ahring, Birgitte K

    2003-04-01

    Linear alkylbenzene sulfonate (LAS) found in wastewater is removed in the wastewater treatment facilities by sorption and aerobic biodegradation. The anaerobic digestion of sewage sludge has not been shown to contribute to the removal. The concentration of LAS based on dry matter typically increases during anaerobic stabilization due to transformation of easily degradable organic matter. Hence, LAS is regarded as resistant to biodegradation under anaerobic conditions. We present data from a lab-scale semi-continuously stirred tank reactor (CSTR) spiked with linear dodecylbenzene sulfonate (C12 LAS), which show that C12 LAS was biodegradable under methanogenic conditions. Sorption of C12 LAS on sewage sludge was described with a Freundlich isotherm. The C12 LAS sorption was determined with different concentrations of total solids (TS). In the semi-continuously stirred tank reactor, 18% of the added C12 LAS was bioavailable and 20% was biotransformed when spiking with 100 mg/L of C12 LAS and a TS concentration of 14.2 mg/L. Enhanced bioavailability of C12 LAS was obtained in an upflow anaerobic sludge blanket (UASB) reactor inoculated with granular sludge and sewage sludge. Biodegradation under thermophilic conditions was 37% with LAS as sole carbon source. Benzaldehyde was produced in the UASB reactor during LAS transformation.

  20. pH-responsive ion transport in polyelectrolyte multilayers of poly(diallyldimethylammonium chloride) (PDADMAC) and poly(4-styrenesulfonic acid-co-maleic acid) (PSS-MA) bearing strong- and weak anionic groups.

    PubMed

    Maza, Eliana; Tuninetti, Jimena S; Politakos, Nikolaos; Knoll, Wolfgang; Moya, Sergio; Azzaroni, Omar

    2015-11-28

    The layer-by-layer construction of interfacial architectures displaying stimuli-responsive control of mass transport is attracting increasing interest in materials science. In this work, we describe the creation of interfacial architectures displaying pH-dependent ionic transport properties which until now have not been observed in polyelectrolyte multilayers. We describe a novel approach to create pH-controlled ion-rectifying systems employing polyelectrolyte multilayers assembled from a copolymer containing both weakly and strongly charged pendant groups, poly(4-styrenesulfonic acid-co-maleic acid) (PSS-MA), alternately deposited with poly(diallyldimethylammonium chloride) (PDADMAC). The conceptual framework is based on the very contrasting and differential interactions of PSS and MA units with PDADMAC. In our setting, sulfonate groups play a structural role by conferring stability to the multilayer due to the strong electrostatic interactions with the polycations, while the weakly interacting MA groups remain "silent" within the film and then act as on-demand pH-responsive units. When these multilayers are combined with a strong cationic capping layer that repels the passage of cationic probes, a pH-gateable rectified transport of anions is observed. Concomitantly, we also observed that these functional properties are significantly affected when multilayers are subjected to extensive pH cycling as a consequence of irreversible morphological changes taking place in the film. We envision that the synergy derived from combining weak and strong interactions within the same multilayer will play a key role in the construction of new interfacial architectures displaying tailorable ion transport properties. PMID:26489595

  1. Modelling of organic field effect transistors with inkjet printed poly(3,4-ethylenedioxythiophene): poly(styrene sulfonate) electrodes: study of the annealing effects.

    PubMed

    Grimaldi, Immacolata Angelica; Del Mauro, Anna de Girolamo; Loffredo, Fausta; Morvillo, Pasquale; Villani, Fulvia

    2013-07-01

    In the present work, the transport mechanism of organic transistors with bottom-gate/top-contact structure, manufactured by employing traditional and inkjet printing techniques, was studied. Poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) conductive polymer was used for realizing printed source, drain and gate electrodes. The influence of the printing parameters (substrate temperature, drop overlapping degree, drop emission frequency) on the uniformity and morphology of the PEDOT:PSS layer was investigated. Polymethyl methacrylate (PMMA) was used as organic dielectric and pentacene, deposited by thermal evaporation, was employed as p-type semiconductor. Organic field effect transistors (OFETs) were fabricated and electrically characterized before and after the thermal annealing process at 120 degrees C for 1 h in nitrogen ambient. The effect of the annealing on the performances of the OFETs was investigated by modelling the measured electrical characteristics and analyzing them in terms of mobility, characteristic temperature and energy distribution of the density of localized states (DOS). In addition, the OFET working under electrical stress in ambient conditions was observed and discussed. PMID:23901549

  2. Morphology, conductivity, and wetting characteristics of PEDOT:PSS thin films deposited by spin and spray coating

    NASA Astrophysics Data System (ADS)

    Zabihi, F.; Xie, Y.; Gao, S.; Eslamian, M.

    2015-05-01

    The goal of this paper is to study the characteristics of PEDOT:PSS thin films and the effects of varying the processing parameters on the structure, functionality, and surface wetting of spun-on and spray-on PEDOT:PSS thin films. PEDOT:PSS is a polymer mixture, which is electrically conductive and transparent and, therefore, is an attractive material for some optoelectronic applications, such as organic and perovskite solar cells. In this work, the films are fabricated using spin coating (a lab-scale method) and spray coating (an up-scalable method). The effects of spinning speed, drying time, and post-annealing temperature on spun-on samples and the effects of the substrate temperature and number of spray passes (deposition layers) on spray-on samples, as well as the effect of precursor solution concentration on both cases are investigated. Various characterization tools, such as AFM, SEM, XRD, confocal laser scanning microscopy (CLSM), and electrical conductivity measurements are used to determine the film roughness, thickness, structure, and morphology. The solution precursor physical data, such as contact angle on glass substrates, viscosity, and interfacial tension, are also obtained within a practical range of temperatures and concentrations. It is found that in both spin and spray coating routes, only well-controlled operating conditions result in the formation of conductive and defect-free PEDOT:PSS films. The formation of PEDOT:PSS thin films with small grains composed of PEDOT forming the core of the grains and PSS forming a shell or coating, which are evenly distributed in a PSS-rich matrix, is favored. Conditions leading to the above-mentioned electrically conductive scenario are identified. Other topics, such as the formation of defects and dewetting, are also elucidated.

  3. Biomimetic shoulder complex based on 3-PSS/S spherical parallel mechanism

    NASA Astrophysics Data System (ADS)

    Hou, Yulei; Hu, Xinzhe; Zeng, Daxing; Zhou, Yulin

    2015-01-01

    The application of the parallel mechanism is still limited in the humanoid robot fields, and the existing parallel humanoid robot joint has not yet been reflected the characteristics of the parallel mechanism completely, also failed to solve the problem, such as small workspace, effectively. From the structural and functional bionic point of view, a three degrees of freedom(DOFs) spherical parallel mechanism for the shoulder complex of the humanoid robot is presented. According to the structure and kinetic characteristics analysis of the human shoulder complex, 3-PSS/S(P for prismatic pair, S for spherical pair) is chosen as the original configuration for the shouder complex. Using genetic algorithm, the optimization of the 3-PSS/S spherical parallel mechanism is performed, and the orientation workspace of the prototype mechanism is enlarged obviously. Combining the practical structure characteristics of the human shouder complex, an offset output mode, which means the output rod of the mechanism turn to any direction at the point a certain distance from the rotation center of the mechanism, is put forward, which provide possibility for the consistent of the workspace of the mechanism and the actual motion space of the human body shoulder joint. The relationship of the attitude angles between different coordinate system is derived, which establishs the foundation for the motion descriptions under different conditions and control development. The 3-PSS/S spherical parallel mechanism is proposed for the shoulder complex, and the consistence of the workspace of the mechanism and the human shoulder complex is realized by the stuctural parameter optimization and the offset output design.

  4. PEDOT:PSS self-assembled films to methanol crossover reduction in Nafion® membranes

    NASA Astrophysics Data System (ADS)

    Almeida, Tiago P.; Miyazaki, Celina M.; Paganin, Valdecir A.; Ferreira, Marystela; Saeki, Margarida J.; Perez, Joelma; Riul, Antonio

    2014-12-01

    Alternative energy sources are on a global demand, with fuel cells as promising devices from mobile to stationary applications. Nafion® is at the heart of many of these appliances, being mostly used due to its high proton conduction and good chemical stability at ambient temperature in proton exchange membranes (PEM). Therefore, methanol permeation throughout Nafion® films reduces drastically the performance of direct methanol fuel cells (DMFC). We present here the deposition of layer-by-layer (LbL) nanostructured thin films of poly(allylamine hydrochloride) (PAH) and poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS) onto commercial Nafion® 212 membranes. It was observed a good adherence of the LbL films onto Nafion® 212, with UV-vis results displaying a linear characteristic growth, indicative that the same amount of material was deposited at each deposition step during the layer-by-layer assembly. In addition, the LbL films also act as a good barrier to avoid methanol crossover, with an observed reduction in the methanol permeation from 5.5 × 10-6 cm2 s-1 to 3.2 × 10-6 cm2 s-1, respectively to pristine Nafion® 212 and a 5-bilayer PAH/PEDOT:PSS LbL film deposited on Nafion®212. The measured power density in a DMFC set-up was not significantly changed (∼12 mW cm-2) due to the LbL films, since the PAH/PEDOT:PSS nanostructure is impeding water and ion transport, consequently affecting the proton conduction throughout the membrane.

  5. Photovoltaic performance of hybrid ITO/PEDOT:PSS/n-SnS/Al solar cell structure

    NASA Astrophysics Data System (ADS)

    Jain, Priyal; Arun, P.

    2016-07-01

    The present paper discusses the performance of ITO/PEDOT:PSS/n-SnS/Al structured solar cells fabricated by thermal evaporation. The performance characterizing parameters such as the open circuit voltage, short circuit current density, series resistance, parallel resistance, ideality factor and the overall efficiency were found to be dependent on the SnS grain size in the nano-meter regime and incident light intensity. The experimental work directly reconfirms the theoretical results and ideas raised in the literature by early researchers.

  6. Ultra fast UV-photo detector based on single-walled carbon nanotube/PEDOT-PSS composites.

    PubMed

    Najeeb, Choolakadavil Khalid; Lee, Jae-Hyoek; Chang, Jingbo; Kang, Won-Seok; Kim, Jae-Ho

    2009-12-01

    Single-walled carbon nanotube (SWNT)/Poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT-PSS), composites (SWNT/PEDOT-PSS) have been prepared using SWNTs surface modified with a natural gum, 'gum arabic' by simple mixing process. Thin films of SWNTs, PEDOT-PSS and the composites were prepared by vacuum filtration technique and were exposed to ultraviolet (UV) radiations for photoconductivity measurements. The surface resistivity of pristine SWNTs film increased from initial value of 50 omega to 92 omega and that of the polymer film decreased from 6.7 Komega to 3.1 Komega while the resistivity of the composite film decreased from 267 omega to 232 omega upon UV illumination. When the lamp was switched off, the initial resistivities of PEDOT: PSS and SWNTs films were recovered very slowly. Interestingly, on the other hand the composite films demonstrated a very fast relaxation within a few minutes. An on-off cycle ruled out the possibility of local heating effect and revealed that the switching property was originated from the fast transport of charge and heat in the composite films. This property of composite film might open up optoelectronic applications involving photoconductivity, such as photo sensors, organic light emitting diodes (OLED) and organic solar cells. Here in, we demonstrate the application of the SWNT/PEDOT-PSS composite film based device as a UV sensor.

  7. Effects of pentacene-doped PEDOT:PSS as a hole-conducting layer on the performance characteristics of polymer photovoltaic cells.

    PubMed

    Kim, Hyunsoo; Lee, Jungrae; Ok, Sunseong; Choe, Youngson

    2012-01-05

    We have investigated the effect of pentacene-doped poly(3,4-ethylenedioxythiophene:poly(4-styrenesulfonate) [PEDOT:PSS] films as a hole-conducting layer on the performance of polymer photovoltaic cells. By increasing the amount of pentacene and the annealing temperature of pentacene-doped PEDOT:PSS layer, the changes of performance characteristics were evaluated. Pentacene-doped PEDOT:PSS thin films were prepared by dissolving pentacene in 1-methyl-2-pyrrolidinone solvent and mixing with PEDOT:PSS. As the amount of pentacene in the PEDOT:PSS solution was increased, UV-visible transmittance also increased dramatically. By increasing the amount of pentacene in PEDOT:PSS films, dramatic decreases in both the work function and surface resistance were observed. However, the work function and surface resistance began to sharply increase above the doping amount of pentacene at 7.7 and 9.9 mg, respectively. As the annealing temperature was increased, the surface roughness of pentacene-doped PEDOT:PSS films also increased, leading to the formation of PEDOT:PSS aggregates. The films of pentacene-doped PEDOT:PSS were characterized by AFM, SEM, UV-visible transmittance, surface analyzer, surface resistance, and photovoltaic response analysis.

  8. Improving the stability of bulk heterojunction solar cells by incorporating pH-neutral PEDOT:PSS as the hole transport layer.

    PubMed

    Meng, Yanhong; Hu, Zhanhao; Ai, Na; Jiang, Zhixiong; Wang, Jian; Peng, Junbiao; Cao, Yong

    2014-04-01

    In the application of traditional bulk heterojunction polymer solar cells, to prevent the etching of ITO by the acidic poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) and thereby improve the device stability, pH-neutral PEDOT:PSS is introduced as the hole transport layer (HTL). After treating the neutral PEDOT:PSS with UV-ozone and with an oxygen plasma, the average power conversion efficiency (PCE) of the device increases from 3.44% to 6.60%. Such surface treatments reduce the energy level offset between the HTL and the active layer, which increases the open circuit voltage and enhances hole transportation, leading to the PCE improvement. Moreover, the devices with the neutral PEDOT:PSS HTL are more stable in air than those with the acidic PEDOT:PSS HTL. The PCE of the devices with the acidic PEDOT:PSS HTL decreases by 20% after 7 days and 45% after 50 days under ambient conditions, whereas the PCE of the devices with the pH-neutral PEDOT:PSS HTL decreases by only 9 and 20% after 7 and 50 days, respectively. X-ray photoelectron spectroscopy shows that the acidic PEDOT:PSS etches the indium from the indium-tin-oxide (ITO) electrode, which is responsible for the degradation of the device. In comparison, the diffusion of the indium is much slower in the devices with the pH-neutral PEDOT:PSS HTL. PMID:24611433

  9. Improving the stability of bulk heterojunction solar cells by incorporating pH-neutral PEDOT:PSS as the hole transport layer.

    PubMed

    Meng, Yanhong; Hu, Zhanhao; Ai, Na; Jiang, Zhixiong; Wang, Jian; Peng, Junbiao; Cao, Yong

    2014-04-01

    In the application of traditional bulk heterojunction polymer solar cells, to prevent the etching of ITO by the acidic poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) and thereby improve the device stability, pH-neutral PEDOT:PSS is introduced as the hole transport layer (HTL). After treating the neutral PEDOT:PSS with UV-ozone and with an oxygen plasma, the average power conversion efficiency (PCE) of the device increases from 3.44% to 6.60%. Such surface treatments reduce the energy level offset between the HTL and the active layer, which increases the open circuit voltage and enhances hole transportation, leading to the PCE improvement. Moreover, the devices with the neutral PEDOT:PSS HTL are more stable in air than those with the acidic PEDOT:PSS HTL. The PCE of the devices with the acidic PEDOT:PSS HTL decreases by 20% after 7 days and 45% after 50 days under ambient conditions, whereas the PCE of the devices with the pH-neutral PEDOT:PSS HTL decreases by only 9 and 20% after 7 and 50 days, respectively. X-ray photoelectron spectroscopy shows that the acidic PEDOT:PSS etches the indium from the indium-tin-oxide (ITO) electrode, which is responsible for the degradation of the device. In comparison, the diffusion of the indium is much slower in the devices with the pH-neutral PEDOT:PSS HTL.

  10. Chitin nanowhisker-supported sulfonated poly(ether sulfone) proton exchange for fuel cell applications.

    PubMed

    Zhang, Chan; Zhuang, Xupin; Li, Xiaojie; Wang, Wei; Cheng, Bowen; Kang, Weimin; Cai, Zhanjun; Li, Mengqin

    2016-04-20

    To balance the relationship among proton conductivity and mechanic strength of sulfonated poly(ether sulfone) (SPES) membrane, chitin nanowhisker-supported nanocomposite membranes were prepared by incorporating whiskers into SPES. The as-prepared chitin whiskers were prepared by 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO) mediated oxidation of α-chitin from crab shells. The structure and properties of the composite membranes were examined as proton exchange membrane (PEM). Results showed that chitin nanowhiskers were dispersed incompactly in the SPES matrix. Thermal stability, mechanical properties, water uptake and proton conductivity of the nanocomposite films were improved from those of the pure SPES film with increasing whisker content, which ascribed to strong interactions between whiskers and between SPES molecules and chitin whiskers via hydrogen bonding. These indicated that composition of filler and matrix got good properties and whisker-supported membranes are promising materials for PEM.

  11. Cycling performance and efficiency of sulfonated poly(sulfone) membranes in vanadium redox flow batteries

    SciTech Connect

    Kim, Soowhan; Yan, Jingling; Schwenzer, Birgit; Zhang, Jianlu; Li, Liyu; Liu, Jun; Yang, Zhenguo; Hickner, Michael A.

    2010-11-30

    As an alternative to the expensive Nafion® ion exchange membrane, an inexpensive commercially-available Radel® polymer was sulfonated, fabricated into a thin membrane, and evaluated for its performance in a vanadium redox flow battery (VRFB). The sulfonated Radel (S-Radel) membrane showed almost an order of magnitude lower permeability of V (IV) ions (2.07×10-7 cm2/min), compared to Nafion 117 (1.29×10-6 cm2/min), resulting in better coulombic efficiency (~98% vs. 95% at 50 mA/cm2) and lower capacity loss per cycle. Even though the S-Radel membrane had slightly higher membrane resistance, the energy efficiency of the VRFB with the S-Radel membrane was comparable to that of Nafion due to its better coulombic efficiency. The S-Radel membrane exhibited good performance up to 40 cycles, but a decay in performance at later cycles was observed.

  12. Chemical and Mechanical Degradation of Sulfonated Poly(sulfone) Membranes in Vanadium Redox Flow Batteries

    SciTech Connect

    Kim, Soowhan; Tighe, Timothy B.; Schwenzer, Birgit; Yan, Jingling; Zhang, Jianlu; Liu, Jun; Yang, Zhenguo; Hickner, Michael A.

    2011-10-01

    A sulfonated poly(sulfone) (S-Radel{reg_sign}) membrane with high proton conductivity and low vanadium ion diffusion showed high initial performance in a vanadium redox flow battery (VRFB) but suffered damage during charge/discharge cycling. The S-Radel membrane had different degradation behaviors in flow cell cycling and ex-situ vanadium ion immersion tests. The S-Radel membrane immersed in V5+ solution cracked into small pieces, but in the VRFB cell, the membrane underwent internal delamination preferentially on the side of the membrane that faced the positive electrode. A vanadium-rich interface was observed near the membrane surface that experienced delamination and Raman spectroscopic analysis of the surfaces of the membrane indicated a slightly depressed 1026 cm-1 band corresponding to the sulfonate SO2 stretch for the degraded surface. Even though the S-Radel membrane underwent severe mechanical damage during the flow cell cycling, significant chemical degradation was not obvious from the spectroscopic analyses. For the VRFB containing an S-Radel membrane, an increase in membrane resistance caused an abnormal voltage depression during the discharge cycle. The reversible increase in membrane resistance and severe mechanical degradation of the membrane during cycling may be attributed repeated formation and dissolution of particles inside the membrane. The mechanical stresses imposed by the particles coupled with a small amount of chemical degradation of the polymer by V5+, are likely degradation mechanisms of the S-Radel membrane in VRFBs under high state-of-charge conditions.

  13. Electrical conductivity of sulfonated poly(ether ether ketone) based composite membranes containing sulfonated polyhedral oligosilsesquioxane

    NASA Astrophysics Data System (ADS)

    Celso, Fabricio; Mikhailenko, Serguei D.; Rodrigues, Marco A. S.; Mauler, Raquel S.; Kaliaguine, Serge

    2016-02-01

    Composite proton exchange membranes (PEMs) intended for fuel cell applications were prepared by embedding of various amounts of dispersed tri-sulfonic acid ethyl POSS (S-Et-POSS) and tri-sulfonic acid butyl POSS (S-Bu-POSS) in thin films of sulfonated poly ether-ether ketone. The electrical properties of the PEMs were studied by Impedance spectroscopy and it was found that their conductivity σ changes with the filler content following a curve with a maximum. The water uptake of these PEMs showed the same dependence. The investigation of initial isolated S-POSS substances revealed the properties of typical electrolytes, which however in both cases possessed low conductivities of 1. 17 × 10-5 S cm-1 (S-Et-POSS) and 3.52 × 10-5 S cm-1 (S-Bu-POSS). At the same time, the insoluble in water S-POSS was found forming highly conductive interface layer when wetted with liquid water and hence producing a strong positive impact on the conductivity of the composite PEM. Electrical properties of the composites were analysed within the frameworks of effective medium theory and bounding models, allowing to evaluate analytically the range of possible conductivity values. It was found that these approaches produced quite good approximation of the experimental data and constituted a fair basis for interpretation of the observed relationship.

  14. Neutron powder diffraction study of perdeuterodimethyl sulfone.

    PubMed

    Ibberson, R M

    2007-05-01

    The crystal structure of perdeuterodimethyl sulfone, (CD(3))(2)SO(2) or C(2)D(6)O(2)S, has been refined at 4.5 K against high-resolution neutron powder diffraction data. The structure determined previously by Sands [Z. Kristallogr. (1963), 119, 245-251] at ambient temperature is shown to remain down to liquid helium temperature, and at 4.5 K the S-C and S-O bond distances are 1.441 (2) and 1.760 (2) A, respectively. The molecules are distorted tetrahedra with C(2v) point symmetry (crystallographic symmetry m2m for S and m for C, O and one D atom) and are linked through a network of weak hydrogen bonds in the C-centred orthorhombic structure.

  15. Reclamation of waste polystyrene by sulfonation

    SciTech Connect

    Inagaki, Yasuhito; Kuromiya, Miyuki; Noguchi, Tsutomu; Watanabe, Haruo

    1999-06-08

    Waste polystyrene containing additives was converted into a polymeric flocculant by a chemical modification. Specifically, waste polystyrene and waste high-impact polystyrene (HI-PS) containing rubber components or a coloring agent were sulfonated to produce a water-soluble polymer whose molecular weight ranged from 400,000 to 700,000. The polymer provides superior purification of the supernatant after flocculating a kaolin suspension than a conventional polymeric flocculant such as a partially hydrolyzed polyacrylamide (hereafter abbreviate PAA). Moreover, using the polymer and a PAA together provides a higher sedimentation rate and a purer supernatant in the treatment of actual wastewater than using each one separately. A new reclamation technology to convert waste plastic into a functional polymer is reported.

  16. Microtexturing of the conductive PEDOT:PSS polymer for superhydrophobic organic electrochemical transistors.

    PubMed

    Gentile, Francesco; Coppedè, Nicola; Tarabella, Giuseppe; Villani, Marco; Calestani, Davide; Candeloro, Patrizio; Iannotta, Salvatore; Di Fabrizio, Enzo

    2014-01-01

    Superhydrophobic surfaces are bioinspired, nanotechnology artifacts, which feature a reduced friction coefficient, whereby they can be used for a number of very practical applications including, on the medical side, the manipulation of biological solutions. In this work, we integrated superhydrophobic patterns with the conducting polymer PEDOT:PSS, one of the most used polymers in organic electronics because highly sensitive to ionized species in solution. In doing so, we combined geometry and materials science to obtain an advanced device where, on account of the superhydrophobicity of the system, the solutions of interest can be manipulated and, on account of the conductive PEDOT:PSS polymer, the charged molecules dispersed inside can be quantitatively measured. This original substrate preparation allowed to perform electrochemical measurements on ionized species in solution with decreasing concentration down to 10(-7) molar. Moreover, it was demonstrated the ability of the device of realizing specific, combined time and space resolved analysis of the sample. Collectively, these results demonstrate how a tight, interweaving integration of different disciplines can provide realistic tools for the detection of pathologies. The scheme here introduced offers breakthrough capabilities that are expected to radically improve both the pace and the productivity of biomedical research, creating an access revolution. PMID:24579079

  17. Inkjet-Printed Graphene/PEDOT:PSS Temperature Sensors on a Skin-Conformable Polyurethane Substrate

    PubMed Central

    Vuorinen, Tiina; Niittynen, Juha; Kankkunen, Timo; Kraft, Thomas M.; Mäntysalo, Matti

    2016-01-01

    Epidermal electronic systems (EESs) are skin-like electronic systems, which can be used to measure several physiological parameters from the skin. This paper presents materials and a simple, straightforward fabrication process for skin-conformable inkjet-printed temperature sensors. Epidermal temperature sensors are already presented in some studies, but they are mainly fabricated using traditional photolithography processes. These traditional fabrication routes have several processing steps and they create a substantial amount of material waste. Hence utilizing printing processes, the EES may become attractive for disposable systems by decreasing the manufacturing costs and reducing the wasted materials. In this study, the sensors are fabricated with inkjet-printed graphene/PEDOT:PSS ink and the printing is done on top of a skin-conformable polyurethane plaster (adhesive bandage). Sensor characterization was conducted both in inert and ambient atmosphere and the graphene/PEDOT:PSS temperature sensors (thermistors) were able reach higher than 0.06% per degree Celsius sensitivity in an optimal environment exhibiting negative temperature dependence. PMID:27752050

  18. Developing the Psychological Strain Scales (PSS): Reliability, Validity, and Preliminary Hypothesis Tests1

    PubMed Central

    Zhang, Jie; Lu, Juncheng; Zhao, Sibo; Lamis, Dorian A.; Li, Ning; Kong, Yuanyuan; Jia, Cunxian; Zhou, Li; Ma, Zhenyu

    2012-01-01

    Since its inception, the Strain Theory of Suicide has been tested and supported in a number of empirical studies. This social psychological theory can be employed as a complementary conceptualization to account for suicidal behaviors as well as mental disorders. However, the lack of consistent measurements of the strains limits the application of the theory in scientific research. Our research team has developed such scales for future testing of the Strain Theory of Suicide in a more systematic approach. For the initial items to measure the four strains (value, aspiration, deprivation, and coping), we solicited approximately 40 items for each strain with high face validity by about 30 fellow researchers. A preliminary examination of about 160 items for consistency and validity, with a sample of about 300 college students, yielded 20 consistent items for each of the four strain scales. Then, a second study was conducted at a different university with approximately 500 students to further streamline each of the four strain scales and test the validity of each with corresponding established scales and variables. As a result, 15 items were selected for each of the four Psychological Strain Scales (PSS). In correlation and multiple regression analyses, we found support for the hypotheses regarding the positive associations between psychological strains measured by the PSS and psychopathology including suicidal ideation. Follow up research with the new scales needs to be carried out in order to test the effects of psychological strains on suicide and mental disorders for various populations. PMID:24443628

  19. Microtexturing of the conductive PEDOT:PSS polymer for superhydrophobic organic electrochemical transistors.

    PubMed

    Gentile, Francesco; Coppedè, Nicola; Tarabella, Giuseppe; Villani, Marco; Calestani, Davide; Candeloro, Patrizio; Iannotta, Salvatore; Di Fabrizio, Enzo

    2014-01-01

    Superhydrophobic surfaces are bioinspired, nanotechnology artifacts, which feature a reduced friction coefficient, whereby they can be used for a number of very practical applications including, on the medical side, the manipulation of biological solutions. In this work, we integrated superhydrophobic patterns with the conducting polymer PEDOT:PSS, one of the most used polymers in organic electronics because highly sensitive to ionized species in solution. In doing so, we combined geometry and materials science to obtain an advanced device where, on account of the superhydrophobicity of the system, the solutions of interest can be manipulated and, on account of the conductive PEDOT:PSS polymer, the charged molecules dispersed inside can be quantitatively measured. This original substrate preparation allowed to perform electrochemical measurements on ionized species in solution with decreasing concentration down to 10(-7) molar. Moreover, it was demonstrated the ability of the device of realizing specific, combined time and space resolved analysis of the sample. Collectively, these results demonstrate how a tight, interweaving integration of different disciplines can provide realistic tools for the detection of pathologies. The scheme here introduced offers breakthrough capabilities that are expected to radically improve both the pace and the productivity of biomedical research, creating an access revolution.

  20. Hybrid device based on GaN nanoneedles and MEH-PPV/PEDOT:PSS polymer

    SciTech Connect

    Shin, Min Jeong; Gwon, Dong-Oh; Lee, Chan-Mi; Lee, Gang Seok; Jeon, In-Jun; Ahn, Hyung Soo; Yi, Sam Nyung; Ha, Dong Han

    2015-08-15

    Highlights: • A hybrid device was demonstrated by using MEH-PPV, PEDOT:PSS, and GaN nanoneedles. • I–V curve of the hybrid device showed its rectification behaviour, similar to a diode. • EL peak originated by the different potential barriers at MEH-PPV and GaN interface. - Abstract: A hybrid device that combines the properties of organic and inorganic semiconductors was fabricated and studied. It incorporated poly[2-methoxy-5-(2-ethylhexyloxy)- 1,4-phenylenevinylene] (MEH-PPV) and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) as organic polymers and GaN nanoneedles as an inorganic semiconductor. Layers of the two polymers were spin coated on to the GaN nanoneedles. The one peak in the electroluminescence spectrum originated from the MEH-PPV layer owing to the different potential barriers of electrons and holes at its interface with the GaN nanoneedles. However, the photoluminescence spectrum showed peaks due to both GaN nanoneedles and MEH-PPV. Such hybrid structures, suitably developed, might be able to improve the efficiency of optoelectronic devices.

  1. Polymer bulk heterojunction solar cells with PEDOT:PSS bilayer structure as hole extraction layer.

    PubMed

    Kim, Wanjung; Kim, Namhun; Kim, Jung Kyu; Park, Insun; Choi, Yeong Suk; Wang, Dong Hwan; Chae, Heeyeop; Park, Jong Hyeok

    2013-06-01

    A high current density obtained in a limited, nanometer-thick region is important for high efficiency polymer solar cells (PSCs). The conversion of incident photons to charge carriers only occurs in confined active layers; therefore, charge-carrier extraction from the active layer within the device by using solar light has an important impact on the current density and the related to power conversion efficiency. In this study, we observed a surprising result, that is, extracting the charge carrier generated in the active layer of a PSC device, with a thickness-controlled PEDOT:PSS bilayer that acted as a hole extraction layer (HEL), yielded a dramatically improved power conversion efficiency in two different model systems (P3HT:PC₆₀BM and PCDTBT:PC₇₀BM). To understand this phenomenon, we conducted optical strength simulation, photocurrent-voltage measurements, incident photon to charge carrier efficiency measurements, ultraviolet photoelectron spectroscopy, and AFM studies. The results revealed that approximately 60 nm was the optimum PEDOT:PSS bilayer HEL thickness in PSCs for producing the maximum power conversion efficiency.

  2. Development of the scale of perceived social support in HIV (PSS-HIV).

    PubMed

    Cortes, Aaron; Hunt, Nigel; McHale, Sue

    2014-12-01

    Social support (SS) plays a key role for HIV/AIDS prevention and disease management. Numerous general and disease-specific SS instruments have been developed and perception of support has been increasingly considered, though no scales have been specifically developed to measure perceived social support (PSS) in HIV/AIDS. To help fill this gap a 12-item scale was developed. The study comprised 406 (HIV(+) and HIV(-)) participants from Chile and the UK. A principal component factor analysis yielded three factors explaining 77.0 % of the total variance: Belonging, Esteem and Self-development with Cronbach α of 0.759, 0.882 and 0.927 respectively and 0.893 on the full scale. The PSS-HIV is brief, easy-to-apply, available in English and Spanish and evaluates the perception of supportive social interactions. Further research is needed to corroborate its capacity to detect psycho-socio-immune interactions, its connection with Maslow's hierarchy of need theory and to evaluate its properties for different health states.

  3. AN/PSS-14 mine detection performance on beaches and in the surf zone

    NASA Astrophysics Data System (ADS)

    Steinway, William J.; Perry, Larry; Maningo, Richard; Ngan, Peter; Locke, Mark

    2004-04-01

    Data collections were conducted using the AN/PSS-14 mine detector on three beach areas in Florida. A few samples of inert anti-tank (AT) and anti-personnel (AP) mines were buried at Jacksonville Beach, Cocoa Beach, and Clearwater Beach. The mines were buried in a variety of sand conditions varying from dry to saturated. The saturated sand conditions included the surf zone with up to two feet of water surge over the buried mine area. Test results indicate a good probability of detection (Pd) of all the buried mines by the AN/PSS-14 Ground Penetration Radar (GPR) and Metal Detector (MD), with a low false alarm rate. This paper will detail test conditions under which the mines were buried, soil dielectric and attenuation parameters measured versus water content in each condition, and interpretation of data in such highly attenuated (400-600 dB attenuation per meter) and extremely conductive soil. In addition, the theory of evanescent electromagnetic waves will be discussed in terms of the performance.

  4. Substantial Improvement of Short Wavelength Response in n-SiNW/PEDOT:PSS Solar Cell

    NASA Astrophysics Data System (ADS)

    Ge, Zhaoyun; Xu, Ling; Cao, Yunqing; Wu, Tao; Song, Hucheng; Ma, Zhongyuan; Xu, Jun; Chen, Kunji

    2015-08-01

    We report herein on the effects of silicon nanowire with different morphology on the device performance of n-SiNW/PEDOT:PSS hybrid solar cells. The power conversion efficiency (PCE) and external quantum efficiency (EQE) of the SiNW/PEDOT:PSS hybrid solar cells can be optimized by varying the length of the silicon nanowires. The optimal length of silicon nanowires is 0.23 μm, and the hybrid solar cell with the optimal length has the V oc of 569 mV, J sc of 30.1 mA/cm2, and PCE of 9.3 %. We fabricated more isolated silicon nanowires with the diluted etching solution. And the J sc of the hybrid solar cell with more isolated nanowires has a significant enhancement, from 30.1 to 33.2 mA/cm2. The remarkable EQE in the wavelength region of 300 and 600 nm was also obtained, which are in excess of 80 %. Our work provides a simple method to substantially improve the EQE of hybrid solar cell in the short wavelength region.

  5. Thermoelectric Properties of Hybrid Thin Films of PEDOT-PSS and Silver Nanowires

    NASA Astrophysics Data System (ADS)

    Yoshida, Akihito; Toshima, Naoki

    2016-06-01

    We report the thermoelectric (TE) properties of organic-inorganic hybrid thin films composed of conductive polymer, poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT-PSS), and inorganic silver nanowire (AgNW). Two kinds of AgNW with different wire length, 3 μm and 27 μm, were used in this study. The AgNW/PEDOT-PSS hybrid films showed an increase in electrical conductivity ( σ) with increase in AgNW concentration. The maximum value of σ obtained in this system was ca. 10,000 S cm-1. The films containing long AgNWs (L-AgNWs) showed higher σ relative to short AgNWs (S-AgNWs) at given concentration, which results from the fact that longer nanowires can easily form a percolated structure. The formation of a percolated structure was confirmed by scanning electron microscopy (SEM) observation. On the other hand, the Seebeck coefficient ( S) of the hybrid films showed the opposite dependence on AgNW concentration. This decrease in S with increasing AgNW concentration is probably because of increase in carrier number due to the AgNWs. These results suggest that the presented organic-inorganic hybrid system is one example where the electrical conductivity and TE properties can be tuned by use of a nanocomposite.

  6. Characteristics of a silicon nanowires/PEDOT:PSS heterojunction and its effect on the solar cell performance.

    PubMed

    Liang, Zhimin; Su, Mingze; Wang, Hao; Gong, Yuting; Xie, Fangyan; Gong, Li; Meng, Hui; Liu, Pengyi; Chen, Huanjun; Xie, Weiguang; Chen, Jian

    2015-03-18

    The interfacial energy-level alignment of a silicon nanowires (SiNWs)/PEDOT:PSS heterojunction is investigated using Kelvin probe force microscopy. The potential difference and electrical distribution in the junction are systematically revealed. When the PEDOT:PSS layer is covered at the bottom of the SiNW array, an abrupt junction is formed at the interface whose characteristics are mainly determined by the uniformly doped Si bulk. When the PEDOT:PSS layer is covered on the top, a hyperabrupt junction localized at the top of the SiNWs forms, and this characteristic depends on the surface properties of the SiNWs. Because the calculation shows that the absorption of light from the SiNWs and the Si bulk are equally important, the bottom-coverage structure leads to better position matching between the depletion and absorption area and therefore shows better photovoltaic performance. The dependence of JSC and VOC on the junction characteristic is discussed.

  7. Alkyl phosphonic acids and sulfonic acids in the Murchison meteorite

    NASA Technical Reports Server (NTRS)

    Cooper, George W.; Onwo, Wilfred M.; Cronin, John R.

    1992-01-01

    Homologous series of alkyl phosphonic acids and alkyl sulfonic acids, along with inorganic orthophosphate and sulfate, are identified in water extracts of the Murchison meteorite after conversion to their t-butyl dimethylsilyl derivatives. The methyl, ethyl, propyl, and butyl compounds are observed in both series. Five of the eight possible alkyl phosphonic acids and seven of the eight possible alkyl sulfonic acids through C4 are identified. Abundances decrease with increasing carbon number as observed of other homologous series indigenous to Murchison. Concentrations range downward from approximately 380 nmol/gram in the alkyl sulfonic acid series, and from 9 nmol/gram in the alkyl phosphonic acid series.

  8. The kinesin AtPSS1 promotes synapsis and is required for proper crossover distribution in meiosis.

    PubMed

    Duroc, Yann; Lemhemdi, Afef; Larchevêque, Cécile; Hurel, Aurélie; Cuacos, Maria; Cromer, Laurence; Horlow, Christine; Armstrong, Susan J; Chelysheva, Liudmila; Mercier, Raphael

    2014-10-01

    Meiotic crossovers (COs) shape genetic diversity by mixing homologous chromosomes at each generation. CO distribution is a highly regulated process. CO assurance forces the occurrence of at least one obligatory CO per chromosome pair, CO homeostasis smoothes out the number of COs when faced with variation in precursor number and CO interference keeps multiple COs away from each other along a chromosome. In several organisms, it has been shown that cytoskeleton forces are transduced to the meiotic nucleus via KASH- and SUN-domain proteins, to promote chromosome synapsis and recombination. Here we show that the Arabidopsis kinesin AtPSS1 plays a major role in chromosome synapsis and regulation of CO distribution. In Atpss1 meiotic cells, chromosome axes and DNA double strand breaks (DSBs) appear to form normally but only a variable portion of the genome synapses and is competent for CO formation. Some chromosomes fail to form the obligatory CO, while there is an increased CO density in competent regions. However, the total number of COs per cell is unaffected. We further show that the kinesin motor domain of AtPSS1 is required for its meiotic function, and that AtPSS1 interacts directly with WIP1 and WIP2, two KASH-domain proteins. Finally, meiocytes missing AtPSS1 and/or SUN proteins show similar meiotic defects suggesting that AtPSS1 and SUNs act in the same pathway. This suggests that forces produced by the AtPSS1 kinesin and transduced by WIPs/SUNs, are required to authorize complete synapsis and regulate maturation of recombination intermediates into COs. We suggest that a form of homeostasis applies, which maintains the total number of COs per cell even if only a part of the genome is competent for CO formation. PMID:25330379

  9. Electrochemical Windows of Sulfone-Based Electrolytes for High-Voltage Li-Ion Batteries

    SciTech Connect

    Shao, Nan; Sun, Xiao-Guang; Dai, Sheng; Jiang, Deen

    2011-01-01

    Further development of high-voltage lithium-ion batteries requires electrolytes with electrochemical windows greater than 5 V. Sulfone-based electrolytes are promising for such a purpose. Here we compute the electrochemical windows for experimentally tested sulfone electrolytes by different levels of theory in combination with various solvation models. The MP2 method combined with the polarizable continuum model is shown to be the most accurate method to predict oxidation potentials of sulfone-based electrolytes with mean deviation less than 0.29 V. Mulliken charge analysis shows that the oxidation happens on the sulfone group for ethylmethyl sulfone and tetramethylene sulfone, and on the ether group for ether functionalized sulfones. Large electrochemical windows of sulfone-based electrolytes are mainly contributed by the sulfone group in the molecules which helps lower the HOMO level. This study can help understand the voltage limits imposed by the sulfone-based electrolytes and aid in designing new electrolytes with greater electrochemical windows.

  10. ITO-free polymer solar cells with inkjet-printed highly-conductive PEDOT:PSS anode

    NASA Astrophysics Data System (ADS)

    Grimaldi, I. A.; Del Mauro, A. De Girolamo; Diana, R.; Loffredo, F.; Morvillo, P.; Villani, F.; Minarini, C.

    2012-07-01

    Actually the most promising polymer solar cell architecture utilizes ITO as transparent conductve anodic electrode. The limited flexibility of ITO and the increasing cost of indium make this kind of electrode not desirable for realizations of low-cost and flexible solar cells. For this reason, it is necessary to develop low-cost, highly flexible and transparent electrodes that can replace the widely used ITO. In this paper, we investigated a new commercial dispersion of PEDOT:PSS suitably modified with dimethyl sulfoxide in solution in order to obtain a highly transparent and conductive manufactured film (HC-PEDOT:PSS) by inkjet printing.

  11. An LQG based PSS design for controlling the SSR in power systems with series-compensated lines

    SciTech Connect

    Seo, J.C.; Kim, T.H.; Park, J.K.; Moon, S.I.

    1996-06-01

    This paper presents a linear quadratic Gaussian (LQG) based power system stabilizer (PSS) to control the subsynchronous resonance (SSR) that may occur in a series capacitor compensated power system. This paper investigates the dominant parameters on the SSR using the critical compensation level (CCL), and selects the design parameters to confirm the stability robustness. The complete SSR simulation system based on the IEEE first benchmark is employed in this study. Eigenvalue analysis and time domain simulations using a nonlinear system model show that the proposed PSS can control the SSR efficiently.

  12. Structure-Property Relationships in Sulfonated Pentablock Copolymers

    NASA Astrophysics Data System (ADS)

    Choi, Jae-Hong; Willis, Carl; Winey, Karen I.

    2011-03-01

    Membranes of pentablock copolymers consisting of poly(tert-butyl styrene) (TBS), hydrogenated polyisoprene (HI), and partially sulfonated poly(styrene-ran-styrene sulfonate) (SS) were studied using small angle X-ray scattering (SAXS) and transmission electron microscopy (TEM). The TBS-HI-SS-HI-TBS pentablock copolymer in solution forms spherical micelles with a core of SS and a corona of solvated HI and TBS. The spherical micelles in solution compact as the solvent evaporates and some of SS cores merge to form interconnected SS microdomains without substantially changing their shape. The number of connections increases with the volume fraction of the SS block, which increases with sulfonation level. The structure does not have long-range order, because strong ionic interactions prevent extensive rearrangement. The morphologies of the sulfonated pentablock copolymers will be correlated with their transport properties.

  13. Affinity labelling enzymes with esters of aromatic sulfonic acids

    DOEpatents

    Wong, Show-Chu; Shaw, Elliott

    1977-01-01

    Novel esters of aromatic sulfonic acids are disclosed. The specific esters are nitrophenyl p- and m-amidinophenylmethanesulfonate. Also disclosed is a method for specific inactivation of the enzyme, thrombin, employing nitrophenyl p-amidinophenylmethanesulfonate.

  14. Spray coated indium-tin-oxide-free organic photodiodes with PEDOT:PSS anodes

    SciTech Connect

    Schmidt, Morten Falco, Aniello; Loch, Marius; Lugli, Paolo; Scarpa, Giuseppe

    2014-10-15

    In this paper we report on Indium Tin Oxide (ITO)-free spray coated organic photodiodes with an active layer consisting of a poly(3-hexylthiophen) (P3HT) and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) blend and patterned poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) electrodes. External quantum efficiency and current voltage characteristics under illuminated and dark conditions as well as cut-off frequencies for devices with varying active and hole conducting layer thicknesses were measured in order to characterize the fabricated devices. 60% quantum efficiency as well as nearly four orders of magnitude on-off ratios have been achieved. Those values are comparable with standard ITO devices.

  15. Magneto-Seebeck effect in an ITO/PEDOT:PSS/Au thin-film device

    NASA Astrophysics Data System (ADS)

    Wang, Hongfeng; Liu, Qing; Tisdale, Jeremy; Xu, Ling; Liu, Yuchun; Hu, Bin

    2016-04-01

    This article reports giant magnetic field effects on the Seebeck coefficient by exerting a Lorentz force on charge diffusion based on vertical multi-layer ITO/PEDOT:PSS/Au thin-film devices. The Lorentz force, induced by an external magnetic field, changes the charge transport and consequently generates angular dependent magnetoresistance. The proposed mechanism of the magneto-Seebeck effect is proved by measuring the magnetoresistance at a parallel, 45o and perpendicular angle to the temperature gradient. The gradual change of the magnetoresistance from a parallel to perpendicular angle indicates that the Lorentz force is a key driving force to develop the magneto-Seebeck effect. Therefore, our experimental results demonstrate a magnetic approach to control the thermoelectric properties in organic materials.

  16. Current-voltage-temperature characteristics of PEDOT:PSS/ZnO thin film-based Schottky barrier diodes

    NASA Astrophysics Data System (ADS)

    Hernandez-Como, N.; Rodriguez-Lopez, A.; Hernandez-Cuevas, F. J.; Munguia, J.; Garcia, R.; Baca-Arroyo, R.; Aleman, M.

    2016-11-01

    In this work, we report the temperature dependence of the electrical parameters of PEDOT:PSS/ZnO Schottky barrier diodes (SBDs) grown on glass substrates. To understand the current conduction mechanism, the current-voltage-temperature characteristics of PEDOT:PSS/ZnO thin film SBDs were studied. The electrical parameters were extracted with both thermionic emission and Cheung models. The obtained Richardson constant and effective barrier height were 5 A cm-2 °K-2 and 0.74 eV, respectively. The diode ideality factor was 1.5 and the series resistance was 36 Ω. All these electrical parameters turned out to be temperature independent which was associated with the dominant transport mechanisms of thermionic emission. The Richardson constant slightly deviates from theoretical values due to the presence of interfacial defects created by the preparation and deposition of PEDOT:PSS and the ZnO film crystallinity. The conductive polymer PEDOT:PSS, as a Schottky contact to ZnO, arises as an alternative to the expensive noble metals: Pt, Pd, Ag and metal oxides: IrOx, PdOx, PtOx.

  17. Flexible, Transparent and Conductive Carbon Nanotube Aerogels /PEDOT:PSS Electrodes created by Top-bottom Fabrication

    NASA Astrophysics Data System (ADS)

    Martinez, Patricia M.; Cerdan Pasaran, Andrea; Zakhidov, Anvar; University of Guanajuato, Mexico Collaboration

    The sheets of Carbon Nanotubes (CNT) have proven to be a good substitute for ITO. To improve their conductivity and increase optical transparency we have created composites which incorporate silver nanowires or other evaporated metals. Coating CNT/metals with PEDOT:PSS is important for creating hole transport/electron barrier layer functionality, but it is not easy to achieve using PEDOT:PSS solutions due to the hydrophobicity of CNT. We report a new top-to-bottom approach for the fabrication of highly flexible, transparent and conductive carbon nanotube-based electrodes using PDMS as a substrate. A uniform and smooth layer of approximately 50 nm of PEDOT:PSS was spin coated on top of a PDMS stamp followed by the deposition of vapor densified freestanding Multiwall Carbon Nanotube (MWNT) aerogels. An incorporation of silver nanowires, silver or Aluminum thin layer can be sprayed or evaporated on top of the freestanding MWNT aerogels in order to lower the sheet resistance even further. The PDMS substrate is drop cast on top of the configuration then the PDMS stamp is lifted-up. The PEDOT:PSS layer is selectively deposited on top of the MWNT only. The composite electrodes can be laminated on photovoltaic devices and on LEDs.

  18. Preparation of Pt/{PDDA-GN/PSS-GN}n multilayer films and their electrocatalytic activity regarding methanol oxidation.

    PubMed

    Huang, Xiaomei; Li, Zhongshui; Zhang, Xiaofeng; He, Xiaolei; Lin, Shen

    2013-03-01

    The stable aqueous dispersion solutions of polymer-modified graphene were prepared by reduction with hydrazine hydrate in situ from exfoliated graphite oxides in the presence of poly (diallyldimethylammonium chloride) (PDDA) and poly(sodium 4-styrenesulfonate) (PSS), respectively. The multilayer films consisting of PDDA-GN and PSS-GN were fabricated on the substrate by layer-by-layer self-assembly technique and characterized by ultraviolet-visible spectroscopy (UV-vis). The multilayer films were used as a novel catalyst support for electrodeposition of Pt nanoparticle clusters in situ. X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscope (FE-SEM), and X-ray diffraction (XRD) analysis demonstrated that Pt particles had been immobilized on the surface of {PDDA-GN/PSS-GN}(n) multilayer films. Cyclic voltammetry and chronoamperometric curves were used to study electrocatalytic activity of Pt/{PDDA-GN/PSS-GN}(n) multilayer films regarding methanol oxidation. The results indicated good electrocatalytic activity of the titled multilayer composites toward methanol oxidation in the 0.5 M H(2)SO(4). PMID:23200343

  19. Ion Exchange Formation via Sulfonated Bicomponent Nonwovens

    NASA Astrophysics Data System (ADS)

    Stoughton, Hannah L.

    For many years ion exchange resins were used to: remove heavy metals from water, recover materials from wastewater, and eliminate harmful gases from the air. While use of these resin beads dominates the ion exchange industry, the beads have limitations that should be considered when decisions are made to employ them. For instance, officials must balance the inherent zero sum surface area and porosity of the materials. This series of studies investigates the use of bicomponent nonwovens as a base substrate for producing high surface area ion exchange materials for the removal of heavy metal ions. Functionalized materials were produced in a two-step process: (1) PET/PE spunbond bicomponent fibers were fractured completely, producing the high surface area nonwoven to be used as the base ion exchange material, and (2) the conditions for functionalizing the PET fibers of the nonwoven webs were investigated where an epoxy containing monomer was grafted to the surface followed by sulfonation of the monomer. The functionalization reactions of the PET fibers were monitored based on: weight gain, FTIR, TOF-SIMS, and SEM. Ion exchange properties were evaluated using titration and copper ion removal capacity from test solutions. The relationship between web structure and removal efficiency of the metal ions was defined through a comparison of the bicomponent and homocomponent nonwovens for copper ion removal efficiency. The investigation revealed that utilizing the high surface area, fractured bicomponent nonwoven ion exchange materials with capacities comparable to commercially available ion exchange resins could be produced.

  20. Dwindling the resistance value of PEDOT:PSS - coated on fabric yarns

    NASA Astrophysics Data System (ADS)

    Amba Sankar K., N.; Mohanta, Kallol

    2016-05-01

    Herein we describe by dip coating method to transform typical fabric yarn to conductive fiber. Different types of yarns have been used to coat from a known conductive polymer, Poly (3,4ethylenedioxythiophene) Poly (styrene sulfonic acid). We have optimized the method to have lesser resistance of the conductive yarns. The minimum resistance achieved has a value of 77 Ω/cm. This value is not high as metals but could be comparable to that of metal oxides or semiconducting materials. However, flexibility of yarns and feeling of fabric combining with the conductivity developed in this process is suitable for wearable electronics and also as gas sensors, electromagnetic shielding.

  1. Studies of the condensation of sulfones with ketones and aldehydes.

    PubMed

    Garst, Michael E; Dolby, Lloyd J; Esfandiari, Shervin; Okrent, Rachel A; Avey, Alfred A

    2006-01-20

    [reaction: see text] The condensation of ketones or aldehydes with sulfones was shown to give a variety of products. Condensation of 2-methylcyclohexanone with dimethyl sulfone using potassium t-butoxide as base gave useful yields of 1,2-dimethylenecyclohexane. Under the same conditions, cycloheptanone, 3-methyl-2-butanone, and 2-butanone were converted to dienes. Remarkably, these reaction conditions converted acetophenone into p-terphenyl (10%) and (E)-1,4-diphenyl-3-penten-1-one (44%). Propiophenone was converted to 2'-methyl-p-terphenyl (61%). Using alpha-tetralone produced 1-methynaphthalene and naphthalene. No reaction took place with beta-tetralone. Using diethyl sulfone with alpha-tetralone lead to pure naphthalene. Condensation of isobutyraldehyde and dimethyl sulfone using potassium t-butoxide gave isoprene in low yield. Using benzaldehyde and benzyl phenyl sulfone in N,N-dimethylacetamide gave 1,2-diphenyl-1-phenylsulfonylethylene, N,N-dimethylcinnamide, and a complex condensation product. Only 1,2-diphenyl-1-phenylsulfonylethylene was obtained when the solvent was THF. PMID:16408963

  2. Sulfonation Pathway Inhibitors Block Reactivation of Latent HIV-1

    PubMed Central

    Murry, Jeffrey P.; Godoy, Joseph; Mukim, Amey; Swann, Justine; Bruce, James W.; Ahlquist, Paul; Bosque, Alberto; Planelles, Vicente; Spina, Celsa A.; Young, John A. T.

    2015-01-01

    Long-lived pools of latently infected cells are a significant barrier to the development of a cure for HIV-1 infection. A better understanding of the mechanisms of reactivation from latency is needed to facilitate the development of novel therapies that address this problem. Here we show that chemical inhibitors of the sulfonation pathway prevent virus reactivation, both in latently infected J-Lat and U1 cell lines and in a primary human CD4+ T cell model of latency. In each of these models, sulfonation inhibitors decreased transcription initiation from the HIV-1 promoter. These inhibitors block transcription initiation at a step that lies downstream of nucleosome remodeling and affects RNA polymerase II recruitment to the viral promoter. These results suggest that the sulfonation pathway acts by a novel mechanism to regulate efficient virus transcription initiation during reactivation from latency, and further that augmentation of this pathway could be therapeutically useful. PMID:25310595

  3. Sulfur and hydrogen isotope anomalies in meteorite sulfonic acids.

    PubMed

    Cooper, G W; Thiemens, M H; Jackson, T L; Chang, S

    1997-08-22

    Intramolecular carbon, hydrogen, and sulfur isotope ratios were measured on a homologous series of organic sulfonic acids discovered in the Murchison meteorite. Mass-independent sulfur isotope fractionations were observed along with high deuterium/hydrogen ratios. The deuterium enrichments indicate formation of the hydrocarbon portion of these compounds in a low-temperature environment that is consistent with that of interstellar clouds. Sulfur-33 enrichments observed in methanesulfonic acid could have resulted from gas-phase ultraviolet irradiation of a precursor, carbon disulfide. The source of the sulfonic acid precursors may have been the reactive interstellar molecule carbon monosulfide.

  4. Sulfur and Hydrogen Isotope Anomalies in Meteorite Sulfonic Acids

    NASA Technical Reports Server (NTRS)

    Cooper, George W.; Thiemens, Mark H.; Jackson, Teresa L.; Chang, Sherwood

    1997-01-01

    Intramolecular carbon, hydrogen, and sulfur isotope ratios were measured on a homologous series of organic sulfonic acids discovered in the Murchison meteorite. Mass-independent sulfur isotope fractionations were observed along with high deuterium/hydrogen ratios. The deuterium enrichments indicate formation of the hydrocarbon portion of these compounds in a low-temperature environment that is consistent with that of interstellar clouds. Sulfur-33 enrichments observed in methanesulfonic acid could have resulted from gas-phase ultraviolet irradiation of a precursor, carbon disulfide. The source of the sulfonic acid precursors may have been the reactive interstellar molecule carbon monosulfide.

  5. Thermal response of transparent silver nanowire/PEDOT:PSS film heaters.

    PubMed

    Ji, Shulin; He, Weiwei; Wang, Ke; Ran, Yunxia; Ye, Changhui

    2014-12-10

    Thermal response behavior of transparent silver nanowire/PEDOT:PSS film heaters are intensively studied for manipulating heating temperature, response time, and power consumption. Influences of substrate heat capacity, heat transfer coefficient between air and heater, sheet resistance and dimension of Ag nanowire film, on the thermal response are investigated from thermodynamic analysis. Suggestion is given for practical applications that if other parameters are fixed, Ag nanowire coverage can be utilized as an effective parameter to adjust the thermal response. The heat transfer coefficient plays opposite roles on thermal response speed and achievable steady temperature. A value of ≈32 W m(-2) K(-1) is obtained from transient process analysis after correcting it by considering heater resistance variation during heating tests. Guidance of designing heaters with a given response time is provided by forming Ag nanowire film with a suitable sheet resistance on substrate of appropriate material and a certain thickness. Thermal response tests of designed Ag heaters are performed to show higher heating temperature, shorter response time, and lower power consumption (179 °C cm(2) W(-1)) than ITO/FTO heaters, as well as homogeneous temperature distribution and stability for repeated use. Potential applications of the Ag heaters in window defogging, sensing and thermochromism are manifested.

  6. Thin Film Silicon Nanowire/PEDOT:PSS Hybrid Solar Cells with Surface Treatment

    NASA Astrophysics Data System (ADS)

    Wang, Hao; Wang, Jianxiong; Hong, Lei; Tan, Yew Heng; Tan, Chuan Seng; Rusli

    2016-06-01

    SiNW/PEDOT:PSS hybrid solar cells are fabricated on 10.6-μm-thick crystalline Si thin films. Cells with Si nanowires (SiNWs) of different lengths fabricated using the metal-catalyzed electroless etching (MCEE) technique have been investigated. A surface treatment process using oxygen plasma has been applied to improve the surface quality of the SiNWs, and the optimized cell with 0.7-μm-long SiNWs achieved a power conversion efficiency (PCE) of 7.83 %. The surface treatment process is found to remove surface defects and passivate the SiNWs and substantially improve the average open circuit voltage from 0.461 to 0.562 V for the optimized cell. The light harvesting capability of the SiNWs has also been investigated theoretically using optical simulation. It is found that the inherent randomness of the MCEE SiNWs, in terms of their diameter and spacing, accounts for the excellent light harvesting capability. In comparison, periodic SiNWs of comparable dimensions have been shown to exhibit much poorer trapping and absorption of light.

  7. Thin Film Silicon Nanowire/PEDOT:PSS Hybrid Solar Cells with Surface Treatment.

    PubMed

    Wang, Hao; Wang, Jianxiong; Hong, Lei; Tan, Yew Heng; Tan, Chuan Seng; Rusli

    2016-12-01

    SiNW/PEDOT:PSS hybrid solar cells are fabricated on 10.6-μm-thick crystalline Si thin films. Cells with Si nanowires (SiNWs) of different lengths fabricated using the metal-catalyzed electroless etching (MCEE) technique have been investigated. A surface treatment process using oxygen plasma has been applied to improve the surface quality of the SiNWs, and the optimized cell with 0.7-μm-long SiNWs achieved a power conversion efficiency (PCE) of 7.83 %. The surface treatment process is found to remove surface defects and passivate the SiNWs and substantially improve the average open circuit voltage from 0.461 to 0.562 V for the optimized cell. The light harvesting capability of the SiNWs has also been investigated theoretically using optical simulation. It is found that the inherent randomness of the MCEE SiNWs, in terms of their diameter and spacing, accounts for the excellent light harvesting capability. In comparison, periodic SiNWs of comparable dimensions have been shown to exhibit much poorer trapping and absorption of light.

  8. Modification of electrical properties of PEDOT:PSS/p-Si heterojunction diodes by doping with dimethyl sulfoxide

    NASA Astrophysics Data System (ADS)

    Pathak, C. S.; Singh, J. P.; Singh, R.

    2016-05-01

    We report about the fabrication and electrical characterization of heterojunction diodes between poly (3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS) doped with dimethyl sulfoxide (DMSO) and p-Si. Electrical characterization of the heterojunction diodes was performed using current-voltage (I-V) measurements. The heterojunction diodes showed good rectifying behavior. Interestingly, for 5 vol.% doping concentration of DMSO, the heterojunction diode showed the best diode characteristics with an ideality factor of 1.9. The doping of DMSO into PEDOT:PSS solution resulted in an increase in the conductivity of films by two orders of magnitude and the films showed high optical transmission (>85%) in the visible region.

  9. High-Performance Flexible All-Solid-State Supercapacitor from Large Free-Standing Graphene-PEDOT/PSS Films

    NASA Astrophysics Data System (ADS)

    Liu, Yuqing; Weng, Bo; Razal, Joselito M.; Xu, Qun; Zhao, Chen; Hou, Yuyang; Seyedin, Shayan; Jalili, Rouhollah; Wallace, Gordon G.; Chen, Jun

    2015-11-01

    Although great attention has been paid to wearable electronic devices in recent years, flexible lightweight batteries or supercapacitors with high performance are still not readily available due to the limitations of the flexible electrode inventory. In this work, highly flexible, bendable and conductive rGO-PEDOT/PSS films were prepared using a simple bar-coating method. The assembled device using rGO-PEDOT/PSS electrode could be bent and rolled up without any decrease in electrochemical performance. A relatively high areal capacitance of 448 mF cm-2 was achieved at a scan rate of 10 mV s-1 using the composite electrode with a high mass loading (8.49 mg cm-2), indicating the potential to be used in practical applications. To demonstrate this applicability, a roll-up supercapacitor device was constructed, which illustrated the operation of a green LED light for 20 seconds when fully charged.

  10. Solvent-treated PEDOT:PSS on the improvement PTB7 based on polymer solar cells performance

    NASA Astrophysics Data System (ADS)

    Huang, Di; Xu, Zheng; Zhao, Suling; Li, Yang; Zhao, Ling; Jin, Shi Qi

    2015-10-01

    In this manuscript, the effect of the 2-propanol(IPA)-treated poly(3,4-ethylenedioxy-thiophene):poly(styrenesulfonate) (PEDOT:PSS) on the performance enhancement of polymer solar cells(PSCs) based on poly[[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b‧]dithiophene-2,6-diyl][3-fluoro-2-[(2-ethylhexyl)carbonyl]thieno[3,4-b]thiophenediyl

  11. Highly conductive PEDOT:PSS on flexible substrate as ITO-free anode for polymer solar cells

    SciTech Connect

    Del Mauro, A. De Girolamo; Ricciardi, R.; Montanino, M.; Morvillo, P.; Minarini, C.

    2014-05-15

    In this work, highly conductive anode based on PEDOT:PSS is proposed as substitute of Indio-Tin Oxide (ITO) in flexible solar cells. The anodic conductive polymer was spin coated on a 125 μm thick polyethylene naphthalate (PEN) substrate. The obtained film was characterized in terms of structure and physical- chemical proprieties. The obtained results are very promising and the conductive film will be investigated in future as electrode in a complete polymeric solar cell.

  12. 40 CFR 417.110 - Applicability; description of the SO3 solvent and vacuum sulfonation subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... solvent and vacuum sulfonation subcategory. 417.110 Section 417.110 Protection of Environment... POINT SOURCE CATEGORY SO3 Solvent and Vacuum Sulfonation Subcategory § 417.110 Applicability; description of the SO3 solvent and vacuum sulfonation subcategory. The provisions of this subpart...

  13. 40 CFR 417.110 - Applicability; description of the SO3 solvent and vacuum sulfonation subcategory.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... solvent and vacuum sulfonation subcategory. 417.110 Section 417.110 Protection of Environment... POINT SOURCE CATEGORY SO3 Solvent and Vacuum Sulfonation Subcategory § 417.110 Applicability; description of the SO3 solvent and vacuum sulfonation subcategory. The provisions of this subpart...

  14. 40 CFR 417.110 - Applicability; description of the SO3 solvent and vacuum sulfonation subcategory.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... solvent and vacuum sulfonation subcategory. 417.110 Section 417.110 Protection of Environment... POINT SOURCE CATEGORY SO3 Solvent and Vacuum Sulfonation Subcategory § 417.110 Applicability; description of the SO3 solvent and vacuum sulfonation subcategory. The provisions of this subpart...

  15. 40 CFR 417.110 - Applicability; description of the SO3 solvent and vacuum sulfonation subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... solvent and vacuum sulfonation subcategory. 417.110 Section 417.110 Protection of Environment... POINT SOURCE CATEGORY SO3 Solvent and Vacuum Sulfonation Subcategory § 417.110 Applicability; description of the SO3 solvent and vacuum sulfonation subcategory. The provisions of this subpart...

  16. 40 CFR 417.110 - Applicability; description of the SO3 solvent and vacuum sulfonation subcategory.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... solvent and vacuum sulfonation subcategory. 417.110 Section 417.110 Protection of Environment... POINT SOURCE CATEGORY SO3 Solvent and Vacuum Sulfonation Subcategory § 417.110 Applicability; description of the SO3 solvent and vacuum sulfonation subcategory. The provisions of this subpart...

  17. 40 CFR 721.6220 - Aryl sulfonate of a fatty acid mixture, polyamine condensate.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Aryl sulfonate of a fatty acid mixture... Specific Chemical Substances § 721.6220 Aryl sulfonate of a fatty acid mixture, polyamine condensate. (a... generically as an aryl sulfonate of a fatty acid mixture, polyamine condensate (PMN P-91-584) is subject...

  18. 40 CFR 721.5425 - α-Olefin sulfonate, potassium salts.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false α-Olefin sulfonate, potassium salts... Substances § 721.5425 α-Olefin sulfonate, potassium salts. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as an α-olefin sulfonate, potassium salt...

  19. 40 CFR 721.6220 - Aryl sulfonate of a fatty acid mixture, polyamine condensate.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Aryl sulfonate of a fatty acid mixture... Specific Chemical Substances § 721.6220 Aryl sulfonate of a fatty acid mixture, polyamine condensate. (a... generically as an aryl sulfonate of a fatty acid mixture, polyamine condensate (PMN P-91-584) is subject...

  20. 40 CFR 721.2565 - Alkylated sulfonated diphenyl oxide, alkali and amine salts.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Alkylated sulfonated diphenyl oxide... New Uses for Specific Chemical Substances § 721.2565 Alkylated sulfonated diphenyl oxide, alkali and... substances identified as alkylated sulfonated diphenyl oxide, alkali salt (PMN P-93-352) and...

  1. 40 CFR 721.950 - Sodium salt of an alkylated, sulfonated aromatic (generic name).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ..., sulfonated aromatic (generic name). 721.950 Section 721.950 Protection of Environment ENVIRONMENTAL... Significant New Uses for Specific Chemical Substances § 721.950 Sodium salt of an alkylated, sulfonated... chemical substance identified generically as a sodium salt of an alkylated, sulfonated aromatic (PMN...

  2. 40 CFR 721.9597 - Salt of a substituted sulfonated aryl azo compound (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Salt of a substituted sulfonated aryl... New Uses for Specific Chemical Substances § 721.9597 Salt of a substituted sulfonated aryl azo... substance identified generically as salt of a substituted sulfonated aryl azo compound (PMN P-00-0094)...

  3. 40 CFR 721.5450 - α-Olefin sulfonate, sodium salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false α-Olefin sulfonate, sodium salt. 721... Substances § 721.5450 α-Olefin sulfonate, sodium salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as α-olefin sulfonate, sodium...

  4. 40 CFR 721.950 - Sodium salt of an alkylated, sulfonated aromatic (generic name).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ..., sulfonated aromatic (generic name). 721.950 Section 721.950 Protection of Environment ENVIRONMENTAL... Significant New Uses for Specific Chemical Substances § 721.950 Sodium salt of an alkylated, sulfonated... chemical substance identified generically as a sodium salt of an alkylated, sulfonated aromatic (PMN...

  5. 40 CFR 721.9597 - Salt of a substituted sulfonated aryl azo compound (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Salt of a substituted sulfonated aryl... New Uses for Specific Chemical Substances § 721.9597 Salt of a substituted sulfonated aryl azo... substance identified generically as salt of a substituted sulfonated aryl azo compound (PMN P-00-0094)...

  6. 40 CFR 721.2565 - Alkylated sulfonated diphenyl oxide, alkali and amine salts.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Alkylated sulfonated diphenyl oxide... New Uses for Specific Chemical Substances § 721.2565 Alkylated sulfonated diphenyl oxide, alkali and... substances identified as alkylated sulfonated diphenyl oxide, alkali salt (PMN P-93-352) and...

  7. 40 CFR 721.5450 - α-Olefin sulfonate, sodium salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false α-Olefin sulfonate, sodium salt. 721... Substances § 721.5450 α-Olefin sulfonate, sodium salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as α-olefin sulfonate, sodium...

  8. 40 CFR 721.9620 - Aromatic sulfonic acid compound with amine.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Aromatic sulfonic acid compound with... Specific Chemical Substances § 721.9620 Aromatic sulfonic acid compound with amine. (a) Chemical substance... aromatic sulfonic acid compound with amine (PMN P-93-832) is subject to reporting under this section...

  9. 40 CFR 721.10437 - Sulfonic acid, linear xylene alkylate, mono, sodium salts (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Sulfonic acid, linear xylene alkylate... Significant New Uses for Specific Chemical Substances § 721.10437 Sulfonic acid, linear xylene alkylate, mono... chemical substances identified generically as sulfonic acid, linear xylene alkylate, mono, sodium...

  10. 40 CFR 721.9620 - Aromatic sulfonic acid compound with amine.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Aromatic sulfonic acid compound with... Specific Chemical Substances § 721.9620 Aromatic sulfonic acid compound with amine. (a) Chemical substance... aromatic sulfonic acid compound with amine (PMN P-93-832) is subject to reporting under this section...

  11. 40 CFR 721.10437 - Sulfonic acid, linear xylene alkylate, mono, sodium salts (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Sulfonic acid, linear xylene alkylate... Significant New Uses for Specific Chemical Substances § 721.10437 Sulfonic acid, linear xylene alkylate, mono... chemical substances identified generically as sulfonic acid, linear xylene alkylate, mono, sodium...

  12. 40 CFR 721.9620 - Aromatic sulfonic acid compound with amine.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Aromatic sulfonic acid compound with... Specific Chemical Substances § 721.9620 Aromatic sulfonic acid compound with amine. (a) Chemical substance... aromatic sulfonic acid compound with amine (PMN P-93-832) is subject to reporting under this section...

  13. 40 CFR 721.9620 - Aromatic sulfonic acid compound with amine.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Aromatic sulfonic acid compound with... Specific Chemical Substances § 721.9620 Aromatic sulfonic acid compound with amine. (a) Chemical substance... aromatic sulfonic acid compound with amine (PMN P-93-832) is subject to reporting under this section...

  14. 40 CFR 721.644 - Amines, C12-14-tert-alkyl, sulfonates.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Amines, C12-14-tert-alkyl, sulfonates... Substances § 721.644 Amines, C12-14-tert-alkyl, sulfonates. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as amines, C12-14-tert-alkyl, sulfonates...

  15. 40 CFR 721.644 - Amines, C12-14-tert-alkyl, sulfonates.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Amines, C12-14-tert-alkyl, sulfonates... Substances § 721.644 Amines, C12-14-tert-alkyl, sulfonates. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as amines, C12-14-tert-alkyl, sulfonates...

  16. 40 CFR 721.644 - Amines, C12-14-tert-alkyl, sulfonates.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Amines, C12-14-tert-alkyl, sulfonates... Substances § 721.644 Amines, C12-14-tert-alkyl, sulfonates. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as amines, C12-14-tert-alkyl, sulfonates...

  17. 40 CFR 721.644 - Amines, C12-14-tert-alkyl, sulfonates.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Amines, C12-14-tert-alkyl, sulfonates... Substances § 721.644 Amines, C12-14-tert-alkyl, sulfonates. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as amines, C12-14-tert-alkyl, sulfonates...

  18. 40 CFR 721.644 - Amines, C12-14-tert-alkyl, sulfonates.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Amines, C12-14-tert-alkyl, sulfonates... Substances § 721.644 Amines, C12-14-tert-alkyl, sulfonates. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as amines, C12-14-tert-alkyl, sulfonates...

  19. 40 CFR 721.10564 - Mixed amino diaryl sulfone isomers (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Mixed amino diaryl sulfone isomers... Specific Chemical Substances § 721.10564 Mixed amino diaryl sulfone isomers (generic). (a) Chemical... as mixed amino diaryl sulfone isomers (PMN P-08-39) is subject to reporting under this section...

  20. 40 CFR 721.10564 - Mixed amino diaryl sulfone isomers (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Mixed amino diaryl sulfone isomers... Specific Chemical Substances § 721.10564 Mixed amino diaryl sulfone isomers (generic). (a) Chemical... as mixed amino diaryl sulfone isomers (PMN P-08-39) is subject to reporting under this section...

  1. 40 CFR 721.9674 - Sulfonated-copper phthalocyanine salt of a triarylmethane dye (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Sulfonated-copper phthalocyanine salt... Significant New Uses for Specific Chemical Substances § 721.9674 Sulfonated-copper phthalocyanine salt of a... chemical substance identified generically as sulfonated-copper phthalocyanine salt of a triarylmethane...

  2. 40 CFR 721.9674 - Sulfonated-copper phthalocyanine salt of a triarylmethane dye (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Sulfonated-copper phthalocyanine salt... Significant New Uses for Specific Chemical Substances § 721.9674 Sulfonated-copper phthalocyanine salt of a... chemical substance identified generically as sulfonated-copper phthalocyanine salt of a triarylmethane...

  3. 40 CFR 721.9674 - Sulfonated-copper phthalocyanine salt of a triarylmethane dye (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Sulfonated-copper phthalocyanine salt... Significant New Uses for Specific Chemical Substances § 721.9674 Sulfonated-copper phthalocyanine salt of a... chemical substance identified generically as sulfonated-copper phthalocyanine salt of a triarylmethane...

  4. 40 CFR 721.9674 - Sulfonated-copper phthalocyanine salt of a triarylmethane dye (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Sulfonated-copper phthalocyanine salt... Significant New Uses for Specific Chemical Substances § 721.9674 Sulfonated-copper phthalocyanine salt of a... chemical substance identified generically as sulfonated-copper phthalocyanine salt of a triarylmethane...

  5. 40 CFR 721.9674 - Sulfonated-copper phthalocyanine salt of a triarylmethane dye (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Sulfonated-copper phthalocyanine salt... Significant New Uses for Specific Chemical Substances § 721.9674 Sulfonated-copper phthalocyanine salt of a... chemical substance identified generically as sulfonated-copper phthalocyanine salt of a triarylmethane...

  6. 40 CFR 721.5425 - α-Olefin sulfonate, potassium salts.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false α-Olefin sulfonate, potassium salts... Substances § 721.5425 α-Olefin sulfonate, potassium salts. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as an α-olefin sulfonate, potassium salt...

  7. 40 CFR 721.9595 - Alkyl benzene sulfonic acids and alkyl sulfates, amine salts (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Alkyl benzene sulfonic acids and alkyl... Significant New Uses for Specific Chemical Substances § 721.9595 Alkyl benzene sulfonic acids and alkyl...) The chemical substances identified generically as alkyl benzene sulfonic acids and alkyl...

  8. 40 CFR 721.9595 - Alkyl benzene sulfonic acids and alkyl sulfates, amine salts (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Alkyl benzene sulfonic acids and alkyl... Significant New Uses for Specific Chemical Substances § 721.9595 Alkyl benzene sulfonic acids and alkyl...) The chemical substances identified generically as alkyl benzene sulfonic acids and alkyl...

  9. 40 CFR 721.9595 - Alkyl benzene sulfonic acids and alkyl sulfates, amine salts (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Alkyl benzene sulfonic acids and alkyl... Significant New Uses for Specific Chemical Substances § 721.9595 Alkyl benzene sulfonic acids and alkyl...) The chemical substances identified generically as alkyl benzene sulfonic acids and alkyl...

  10. 40 CFR 721.9595 - Alkyl benzene sulfonic acids and alkyl sulfates, amine salts (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Alkyl benzene sulfonic acids and alkyl... Significant New Uses for Specific Chemical Substances § 721.9595 Alkyl benzene sulfonic acids and alkyl...) The chemical substances identified generically as alkyl benzene sulfonic acids and alkyl...

  11. 40 CFR 721.9595 - Alkyl benzene sulfonic acids and alkyl sulfates, amine salts (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Alkyl benzene sulfonic acids and alkyl... Significant New Uses for Specific Chemical Substances § 721.9595 Alkyl benzene sulfonic acids and alkyl...) The chemical substances identified generically as alkyl benzene sulfonic acids and alkyl...

  12. 40 CFR 721.9620 - Aromatic sulfonic acid compound with amine.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Aromatic sulfonic acid compound with... Specific Chemical Substances § 721.9620 Aromatic sulfonic acid compound with amine. (a) Chemical substance... aromatic sulfonic acid compound with amine (PMN P-93-832) is subject to reporting under this section...

  13. 40 CFR 721.5450 - α-Olefin sulfonate, sodium salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false α-Olefin sulfonate, sodium salt. 721... Substances § 721.5450 α-Olefin sulfonate, sodium salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as α-olefin sulfonate, sodium...

  14. 40 CFR 721.5425 - α-Olefin sulfonate, potassium salts.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false α-Olefin sulfonate, potassium salts... Substances § 721.5425 α-Olefin sulfonate, potassium salts. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as an α-olefin sulfonate, potassium salt...

  15. 40 CFR 721.5425 - α-Olefin sulfonate, potassium salts.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false α-Olefin sulfonate, potassium salts... Substances § 721.5425 α-Olefin sulfonate, potassium salts. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as an α-olefin sulfonate, potassium salt...

  16. 40 CFR 721.5450 - α-Olefin sulfonate, sodium salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false α-Olefin sulfonate, sodium salt. 721... Substances § 721.5450 α-Olefin sulfonate, sodium salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as α-olefin sulfonate, sodium...

  17. 40 CFR 721.5450 - α-Olefin sulfonate, sodium salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false α-Olefin sulfonate, sodium salt. 721... Substances § 721.5450 α-Olefin sulfonate, sodium salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as α-olefin sulfonate, sodium...

  18. 40 CFR 721.5425 - α-Olefin sulfonate, potassium salts.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false α-Olefin sulfonate, potassium salts... Substances § 721.5425 α-Olefin sulfonate, potassium salts. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as an α-olefin sulfonate, potassium salt...

  19. 40 CFR 721.10474 - Substituted amino ethane sulfonic acid salt (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Substituted amino ethane sulfonic acid... Specific Chemical Substances § 721.10474 Substituted amino ethane sulfonic acid salt (generic). (a... generically as substituted amino ethane sulfonic acid salt (PMN P-04-107) is subject to reporting under...

  20. 40 CFR 721.10474 - Substituted amino ethane sulfonic acid salt (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Substituted amino ethane sulfonic acid... Specific Chemical Substances § 721.10474 Substituted amino ethane sulfonic acid salt (generic). (a... generically as substituted amino ethane sulfonic acid salt (PMN P-04-107) is subject to reporting under...

  1. 40 CFR 721.10633 - Aromatic sulfonic acid amino azo dye salts (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Aromatic sulfonic acid amino azo dye... Specific Chemical Substances § 721.10633 Aromatic sulfonic acid amino azo dye salts (generic). (a) Chemical... as aromatic sulfonic acid amino azo dye salts (PMN P-12-276) is subject to reporting under...

  2. 40 CFR 721.6220 - Aryl sulfonate of a fatty acid mixture, polyamine condensate.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Aryl sulfonate of a fatty acid mixture... Specific Chemical Substances § 721.6220 Aryl sulfonate of a fatty acid mixture, polyamine condensate. (a... generically as an aryl sulfonate of a fatty acid mixture, polyamine condensate (PMN P-91-584) is subject...

  3. 40 CFR 721.6220 - Aryl sulfonate of a fatty acid mixture, polyamine condensate.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Aryl sulfonate of a fatty acid mixture... Specific Chemical Substances § 721.6220 Aryl sulfonate of a fatty acid mixture, polyamine condensate. (a... generically as an aryl sulfonate of a fatty acid mixture, polyamine condensate (PMN P-91-584) is subject...

  4. 40 CFR 721.6220 - Aryl sulfonate of a fatty acid mixture, polyamine condensate.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Aryl sulfonate of a fatty acid mixture... Specific Chemical Substances § 721.6220 Aryl sulfonate of a fatty acid mixture, polyamine condensate. (a... generically as an aryl sulfonate of a fatty acid mixture, polyamine condensate (PMN P-91-584) is subject...

  5. pHEMA Encapsulated PEDOT-PSS-CNT Microsphere Microelectrodes for Recording Single Unit Activity in the Brain

    PubMed Central

    Castagnola, Elisa; Maggiolini, Emma; Ceseracciu, Luca; Ciarpella, Francesca; Zucchini, Elena; De Faveri, Sara; Fadiga, Luciano; Ricci, Davide

    2016-01-01

    The long-term reliability of neural interfaces and stability of high-quality recordings are still unsolved issues in neuroscience research. High surface area PEDOT-PSS-CNT composites are able to greatly improve the performance of recording and stimulation for traditional intracortical metal microelectrodes by decreasing their impedance and increasing their charge transfer capability. This enhancement significantly reduces the size of the implantable device though preserving excellent electrical performances. On the other hand, the presence of nanomaterials often rises concerns regarding possible health hazards, especially when considering a clinical application of the devices. For this reason, we decided to explore the problem from a new perspective by designing and testing an innovative device based on nanostructured microspheres grown on a thin tether, integrating PEDOT-PSS-CNT nanocomposites with a soft synthetic permanent biocompatible hydrogel. The pHEMA hydrogel preserves the electrochemical performance and high quality recording ability of PEDOT-PSS-CNT coated devices, reduces the mechanical mismatch between soft brain tissue and stiff devices and also avoids direct contact between the neural tissue and the nanocomposite, by acting as a biocompatible protective barrier against potential nanomaterial detachment. Moreover, the spherical shape of the electrode together with the surface area increase provided by the nanocomposite deposited on it, maximize the electrical contact and may improve recording stability over time. These results have a good potential to contribute to fulfill the grand challenge of obtaining stable neural interfaces for long-term applications. PMID:27147944

  6. WO3 nanopaticles and PEDOT:PSS/WO3 composite thin films studied for photocatalytic and electrochromic applications

    NASA Astrophysics Data System (ADS)

    Ivanov Boyadjiev, Stefan; Manduca, Bruno; Szűcs, Júlia; Miklós Szilágyi, Imre

    2016-03-01

    WO3 is a widely studied material for electrochromic and photocatalytic applications. In the present study, WO3 nanoparticles with a controlled structure (monoclinic or hexagonal) were obtained by controlled thermal decomposition of hexagonal ammonium tungsten bronze in air at 500 °C and 600 °C, respectively. The formation, morphology, structure and composition of the as-prepared nanoparticles were studied by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), and scanning electron microscopy combined with energy-dispersive X-ray spectroscopy (SEM-EDX). The photocatalytic activity of the monoclinic and hexagonal WO3 nanoparticles was studied by decomposing methyl orange in aqueous solution under UV light irradiation. In order to study the electrochromic properties of the WO3 nanoparticles, as well to introduce them for self-cleaning photocatalytic surface applications, thin films were prepared from the WO3 particles together with a conductive polymer. For this, PEDOT:PSS was used, which gives excellent opportunities for obtaining transparent and conductive thin films, suitable for both electrochromic and photocatalytic applications. By spin-coating, transparent PEDOT:PSS/WO3 composite thin films were prepared, on which cyclic voltammetry measurements were performed, and the coloring and bleaching states were studied. Our initial results for the PEDOT:PSS/WO3 composite thin films are promising, suggesting that such composites, after further development, might be successfully used in electrochromic devices and photocatalysis.

  7. PEDOT:PSS with embedded TiO2 nanoparticles as light trapping electrode for organic photovoltaics

    NASA Astrophysics Data System (ADS)

    Park, Yoonseok; Müller-Meskamp, Lars; Vandewal, Koen; Leo, Karl

    2016-06-01

    The performance of organic optoelectronic devices can be improved by employing a suitable optical cavity design beyond the standard plane layer approach, e.g., by the inclusion of periodically or randomly textured structures which increase light incoupling or extraction. One of the simplest approaches is to add an additional layer containing light scattering particles into the device stack. Solution processed poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) thin films are promising for replacing the brittle and expensive indium tin oxide transparent electrode. We use a blend of 100 nm TiO2 scattering particles in PEDOT:PSS solution to fabricate transparent electrode films which also functions as a scattering layer. When utilized in an organic photovoltaic device, a power conversion efficiency of 7.92% is achieved, which is an 8.6% relative improvement compared to a device with a neat PEDOT:PSS electrode without the nanoparticles. This improvement is caused by an increase in short-circuit current due to an improved photon harvesting in the 320 nm-700 nm spectral wavelength range.

  8. Porous spherical CaO-based sorbents via PSS-assisted fast precipitation for CO2 capture.

    PubMed

    Wang, Shengping; Fan, Lijing; Li, Chun; Zhao, Yujun; Ma, Xinbin

    2014-10-22

    In this paper, we report the development of synthetic CaO-based sorbents via a fast precipitation method with the assistance of sodium poly(styrenesulfonate) (PSS). The effect of PSS on physical properties of the CaO sorbents and their CO2 capture performance were investigated. The presence of PSS dispersed the CaO particles effectively as well as increased their specific surface area and pore volume remarkably. The obtained porous spherical structure facilitated CO2 to diffuse and react with inner CaO effectively, resulting in a significant improvement in initial CO2 carbonation capacity. A proper amount of Mg(2+) precursor solution was doped during a fast precipitation process to gain CaO-based sorbents with a high anti-sintering property, which maintained the porous spherical structure with the high specific surface area. CaO-based sorbents derived from a MgxCa1-xCO3 precursor existed in the form of CaO and MgO. The homogeneous distribution of MgO in the CaO-based sorbents effectively prevented the CaO crystallite from growing and sintering, further resulting in the favorable long-term durability with carbonation capacity of about 52.0% after 30 carbonation/calcination cycles.

  9. pHEMA Encapsulated PEDOT-PSS-CNT Microsphere Microelectrodes for Recording Single Unit Activity in the Brain.

    PubMed

    Castagnola, Elisa; Maggiolini, Emma; Ceseracciu, Luca; Ciarpella, Francesca; Zucchini, Elena; De Faveri, Sara; Fadiga, Luciano; Ricci, Davide

    2016-01-01

    The long-term reliability of neural interfaces and stability of high-quality recordings are still unsolved issues in neuroscience research. High surface area PEDOT-PSS-CNT composites are able to greatly improve the performance of recording and stimulation for traditional intracortical metal microelectrodes by decreasing their impedance and increasing their charge transfer capability. This enhancement significantly reduces the size of the implantable device though preserving excellent electrical performances. On the other hand, the presence of nanomaterials often rises concerns regarding possible health hazards, especially when considering a clinical application of the devices. For this reason, we decided to explore the problem from a new perspective by designing and testing an innovative device based on nanostructured microspheres grown on a thin tether, integrating PEDOT-PSS-CNT nanocomposites with a soft synthetic permanent biocompatible hydrogel. The pHEMA hydrogel preserves the electrochemical performance and high quality recording ability of PEDOT-PSS-CNT coated devices, reduces the mechanical mismatch between soft brain tissue and stiff devices and also avoids direct contact between the neural tissue and the nanocomposite, by acting as a biocompatible protective barrier against potential nanomaterial detachment. Moreover, the spherical shape of the electrode together with the surface area increase provided by the nanocomposite deposited on it, maximize the electrical contact and may improve recording stability over time. These results have a good potential to contribute to fulfill the grand challenge of obtaining stable neural interfaces for long-term applications. PMID:27147944

  10. Study of PEDOT: PSS and BCP thicknesses effect on SubPc/C60 organic solar cell efficiency

    NASA Astrophysics Data System (ADS)

    Mendil, Nesrine; Daoudi, Mebarka; Berkai, Zakarya; Belghachi, Abderrahmane

    2015-09-01

    A high-performance of a planar hetejunction structure is demonstrated by using Fullerene (C60) and Boron Subphthalocyanine Chloride (SubPc) sandwiched between a cathode and an anode, indium tin oxide (ITO) and aluminum (Al), respectively. Often, there will also exist a buffer layer such as Poly 3,4-EthyleneDioxyThiophene : Poly- Styrene Sulphonate (PEDOT:PSS) and Bathocuproine (BCP) between any active layer and adjacent electrode, which is responsible for increasing efficiency through modifying the work function and controlling exciton diffusion. The cell that we studied is composed of the following structure: ITO(30nm)/PEDOT:PSS(xnm)/SubPc(25nm)/C60(35nm)/BCP(ynm)/Al(30nm), with different value of x=5,10,12,15,20 nm and y=8,10,12,14,16nm. So, the aim of our work is to investigate the effect of PEDOT: PSS and BCP thicknesses on the efficiency of this organic solar cell.

  11. pHEMA Encapsulated PEDOT-PSS-CNT Microsphere Microelectrodes for Recording Single Unit Activity in the Brain.

    PubMed

    Castagnola, Elisa; Maggiolini, Emma; Ceseracciu, Luca; Ciarpella, Francesca; Zucchini, Elena; De Faveri, Sara; Fadiga, Luciano; Ricci, Davide

    2016-01-01

    The long-term reliability of neural interfaces and stability of high-quality recordings are still unsolved issues in neuroscience research. High surface area PEDOT-PSS-CNT composites are able to greatly improve the performance of recording and stimulation for traditional intracortical metal microelectrodes by decreasing their impedance and increasing their charge transfer capability. This enhancement significantly reduces the size of the implantable device though preserving excellent electrical performances. On the other hand, the presence of nanomaterials often rises concerns regarding possible health hazards, especially when considering a clinical application of the devices. For this reason, we decided to explore the problem from a new perspective by designing and testing an innovative device based on nanostructured microspheres grown on a thin tether, integrating PEDOT-PSS-CNT nanocomposites with a soft synthetic permanent biocompatible hydrogel. The pHEMA hydrogel preserves the electrochemical performance and high quality recording ability of PEDOT-PSS-CNT coated devices, reduces the mechanical mismatch between soft brain tissue and stiff devices and also avoids direct contact between the neural tissue and the nanocomposite, by acting as a biocompatible protective barrier against potential nanomaterial detachment. Moreover, the spherical shape of the electrode together with the surface area increase provided by the nanocomposite deposited on it, maximize the electrical contact and may improve recording stability over time. These results have a good potential to contribute to fulfill the grand challenge of obtaining stable neural interfaces for long-term applications.

  12. Flexible white phosphorescent organic light emitting diodes based on multilayered graphene/PEDOT:PSS transparent conducting film

    NASA Astrophysics Data System (ADS)

    Wu, Xiaoxiao; Li, Fushan; Wu, Wei; Guo, Tailiang

    2014-03-01

    A double-layered graphene/poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) conductive film was prepared, in which the PEDOT:PSS layer was obtained by using spray-coating technique. A flexible white phosphorescent organic light-emitting devices based on the graphene/PEDOT:PSS conductive film was fabricated. Phosphorescent material tris(2-phenylpyridine) iridium (Ir(ppy)3) and the fluorescent dye 5,6,11,12-tetraphenylnapthacene (Rubrene) were co-doped into 4,4‧-N,N‧-dicarbazole-biphenyl (CBP) host. N,N‧-diphenyl-N,N‧-bis(1-naphthyl)-(1,1‧-biphenyl)-4,4‧-diamine (NPB) and 4,7-diphenyl-1,10-phenanthroline (Bphen) were used as hole-transporting and electron-transporting layer, respectively, and 4,4‧-bis(2,2‧-diphenylvinyl)-1,1‧-biphenyl (DPVBi) was used as blue light-emitting layer. The device presented pure white light emission with a Commission Internationale De I'Eclairage coordinates of (0.31, 0.33) and exhibited an excellent light-emitting stability during the bending cycle test with a radius of curvature of 10 mm.

  13. 21 CFR 177.2210 - Ethylene polymer, chloro-sulfonated.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ethylene polymer, chloro-sulfonated. 177.2210... (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use Only as Components of Articles Intended for Repeated Use § 177.2210 Ethylene polymer,...

  14. 21 CFR 177.2210 - Ethylene polymer, chloro-sulfonated.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Ethylene polymer, chloro-sulfonated. 177.2210... (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use Only as Components of Articles Intended for Repeated Use § 177.2210 Ethylene polymer,...

  15. Identification of sulfonic acids as efficient ecto-5'-nucleotidase inhibitors.

    PubMed

    Iqbal, Jamshed; Saeed, Aamer; Raza, Rabia; Matin, Abdul; Hameed, Abdul; Furtmann, Norbert; Lecka, Joanna; Sévigny, Jean; Bajorath, Jürgen

    2013-01-01

    Ecto-5'-nucleotidase (CD73) is well known for its implication in cancer. Inhibition of ecto-5'-nucleotidases is thought to provide an attractive approach to cancer therapy. This study identifies sulfonic acid compounds as efficient inhibitors of ecto-5'-nucleotidases. The compounds were tested against recombinant human and rat ecto-5'-nucleotidases. The most potent new sulfonic acid inhibitor 6-amino-4-hydroxynaphthalene-2-sulfonic acid (1) of ecto-5'-nucleotidase had an IC₅₀ of 1.32 ± 0.09 μM for the human and 10.4 ± 3.3 μM for the rat enzyme. Generally, all compounds were more active against the human enzyme. Plausible binding mode models were developed for this new class of inhibitors. Furthermore, several sulfonic acid inhibitors were efficient cytotoxic agents when tested on H157 cancer cell lines. Hence, new ecto-5'-nucleotidases inhibitors displayed significant potential for further development as compounds for anti-cancer therapy.

  16. Complexes of poly-N-vinylpyrrolidone with sulfonated tetraphenylporphins

    SciTech Connect

    Kulvelis, Yu. V. Lebedev, V. T.; Toeroek, Gy.; Klyubin, V. V.

    2007-05-15

    The interaction of sulfonated tetraphenylporphins H{sub 2}TPPS{sub 4}(HCl){sub 2} and in CuTPPS{sub 4} with poly-N-vinylpyrrolidone (PVP) is studied using small-angle neutron scattering, dynamic light scattering, visible spectrophotometry, and viscometry. It is shown that porphyrin molecules form complexes with PVP, thus charging the polymeric chain.

  17. Toxicokinetics of perfluorooctane sulfonate in rainbow trout (Oncorhynchus mykiss)

    EPA Science Inventory

    Rainbow trout (Oncorhynchus mykiss) confined to respirometer-metabolism chambers were dosed with perfluorooctane sulfonate (PFOS) by intra-arterial injection and sampled to obtain concentration time-course data for plasma, and either urine or expired water. The data were then an...

  18. EVALUATION OF PERFLUOROOCTANE SULFONATE IN THE RAT BRAIN

    EPA Science Inventory

    Perfluorooctane Sulfonate (PFOS) is an environmentally persistent chemical that has been detected in humans and wildlife. PFOS is primarily distributed in liver and blood. The current study evaluated the level of PFOS in the adult and neonatal rat brain and determined whether t...

  19. Use of amine neutralized sulfonated polystyrenes for particle flocculation

    SciTech Connect

    Mintz, D.J.; Peiffer, D.G.; Thaler, W.A.; Duvdevani, I.

    1987-10-20

    A process is described for flocculating solid fines selected from the group consisting of coke films, catalyst fines, synthetic fuel fines, coal fines, and shale fines from a solution comprising the solid fines and an organic liquid which comprises the steps of: (a) adding with mixing about 5 to about 10,000 ppm of the water insoluble unneutralized or neutralized sulfonated polystyrene to the solution wherein the sulfonated polystyrene is dissolved in a dissolving organic liquid at a concentration level of about 0.01 to about 20 weight percent, and has about 0.5 to about 100 mole percent of sulfonate groups; and (b) heating at about 25/sup 0/C to about 350/sup 0/C for about 1 to about 45 minutes the mixture of the solution and the unneutralized or neutralized polystyrene wherein the sulfonated polystrene is absorbed on the surface of the solid fines, and the solid fines collide to form agglomerates which precipitate out of the solution.

  20. PERFLUOROOCTANE SULFONATE (PFOS) DISRUPTS THE THYROID STATUS IN LABORATORY RODENTS

    EPA Science Inventory

    PERFLUOROOCTANE SULFONATE (PFOS) DISRUPTS THE THYROID STATUS IN LABORATORY RODENTS. C. Lau, J.R. Thibodeaux, R.G. Hanson, B.E. Gray and J.M. Rogers. Reprod. Tox. Div. NHEERL, US EPA, Research Triangle Park, NC.

    PFOS is an environmental contaminant ubiquitously found in h...

  1. Epoxy-crosslinked sulfonated poly (phenylene) copolymer proton exchange membranes

    DOEpatents

    Hibbs, Michael; Fujimoto, Cy H.; Norman, Kirsten; Hickner, Michael A.

    2010-10-19

    An epoxy-crosslinked sulfonated poly(phenylene) copolymer composition used as proton exchange membranes, methods of making the same, and their use as proton exchange membranes (PEM) in hydrogen fuel cells, direct methanol fuel cell, in electrode casting solutions and electrodes, and in sulfur dioxide electrolyzers. These improved membranes are tougher, have higher temperature capability, and lower SO.sub.2 crossover rates.

  2. 21 CFR 177.2500 - Polyphenylene sulfone resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyphenylene sulfone resins. 177.2500 Section 177.2500 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use Only...

  3. 21 CFR 177.2500 - Polyphenylene sulfone resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyphenylene sulfone resins. 177.2500 Section 177.2500 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use Only...

  4. 21 CFR 177.2500 - Polyphenylene sulfone resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyphenylene sulfone resins. 177.2500 Section 177.2500 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use Only as Components of Articles Intended for...

  5. Absorption and distribution of perfluorooctane sulfonate (PFOS) in beef cattle

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Perfluorooctane sulfonate (PFOS) is an industrial chemical that is found in biosolids, and the application of these biosolids to pastures has raised concerns about human exposure through the accumulation of PFOS in edible tissues of these animals. The United States Department of Agriculture (USDA) h...

  6. Hydrogen-bonding patterns in pyrimethaminium pyridine-3-sulfonate

    PubMed Central

    Nirmalram, Jeyaraman Selvaraj; Thomas Muthiah, Packianathan

    2010-01-01

    In the asymmetric unit of the title salt [systematic name: 2,4-diamino-5-(4-chloro­phen­yl)-6-ethyl­pyrimidin-1-ium pyri­dine-3-sulfonate], C12H14N4Cl+·C5H4NSO3 −, there are two independent pyrimethaminium cations and two 3-pyridine sulfonate anions. Each sulfonate group inter­acts with the corresponding protonated pyrimidine ring through two N—H⋯O hydrogen bonds, forming a cyclic hydrogen-bonded bimolecular R 2 2(8) motif. Even though the primary mode of association is the same, the next higher level of supra­molecular architectures are different due to different hydrogen-bonded networks. In one of the independent molecules in the asymmetric unit, the pyrimethamine cation is paired centrosymmetrically through N—H⋯N hydrogen bonds, generating an R 2 2(8) ring motif. In the other molecule, the pyrimethamine cation does not form any base pairs; instead it forms hydrogen bonds with the 3-pyridine sulfonate anion. The structure is further stabilized by C—H⋯O, C—H⋯N and π–π stacking [centroid–centroid distance = 3.9465 (13) Å] inter­actions. PMID:21588411

  7. 21 CFR 177.2210 - Ethylene polymer, chloro-sulfonated.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ethylene polymer, chloro-sulfonated. 177.2210... (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use Only as Components of Articles Intended for Repeated Use § 177.2210 Ethylene polymer,...

  8. 21 CFR 177.2210 - Ethylene polymer, chloro-sulfonated.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ethylene polymer, chloro-sulfonated. 177.2210... (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use Only as Components of Articles Intended for Repeated Use § 177.2210 Ethylene polymer,...

  9. Pyrolysis Pathways of Sulfonated Polyethylene, an Alternative Carbon Fiber Precursor

    SciTech Connect

    Younker, Jarod M; Saito, Tomonori; Hunt, Marcus A; Beste, Ariana; Naskar, Amit K

    2013-01-01

    Sulfonated polyethylene is an emerging precursor for the production of carbon fibers. Pyrolysis of sulfonated polyethylene was characterized by thermogravimetric analysis (TGA). n-heptane-4-sulfonic acid (H4S) was selected as a model compound for the study of sulfonated polyethylene. Density functional theory and conventional transition state theory were used to determine the rate constants of pyrolysis for H4S from 300-1000 K. Multiple reaction channels from two different mechanisms were explored: 1) internal five-centered elimination (Ei 5) and 2) radical chain reaction. The pyrolysis of H4S was simulated with kinetic Monte Carlo (kMC) to obtain TGA plots that compared favorably to experiment. We observed that at tem- peratures < 550 K, the radical mechanism was dominant and yielded the trans-alkene, whereas cis-alkene was formed at higher temperatures from the internal elimination. The maximum rates of % mass loss became independent of initial OH radical concentration at 440-480 K. Experimentally, the maximum % mass loss occurred from 440-460 K (heating rate dependent). Activation energies derived from the kMC-simulated TGAs of H4S (26-29 kcal/mol) agreed with experiment for sulfonated polyethylene ( 31 kcal/mol). The simulations revealed that in this region, decomposition of radical HOSO2 became competitive to H abstraction by HOSO2, making OH the carrying radical for the reaction chain. The maximum rate of % mass loss for internal elimination was observed at temperatures > 600 K. Low-scale carbonization utilizes temperatures < 620 K; thus, internal elimination will not be competitive. Ei5 elimination has been studied for sulfoxides and sulfones, but this represents the first study of internal elimination in sulfonic acids. Nonlinear Arrhenius plots were found for all bimolecular reactions. The most significant nonlinear behavior was observed for reactions where the barrier was small. For reactions with low activation barriers, nonlinearity was traced to

  10. Maskless selective laser patterning of PEDOT:PSS on barrier/foil for organic electronics applications

    NASA Astrophysics Data System (ADS)

    Karnakis, Dimitris; Stephens, Tim; Chabrol, Gregoire

    2013-03-01

    Rapid developments in organic electronics promise low cost devices for applications such as OLED, organic transistors and organic photovoltaics on large-area glass or flexible substrates in the near future. The technology is very attractive as most device layers can be solution printed. But when directly patterned deposition is impossible, a post-patterning step is required and laser processing is gradually emerging as a key-enabling tool. DPSS lasers offer several advantages including maskless, non-contact, dry patterning, but also scalable large area processing, well suited to roll-to-roll manufacturing at μm resolutions. However, very few reports discuss in detail the merits of DPSS laser patterning technology, especially on flexible substrates. This paper describes the potential of ultrafast DPSS laser technology for OLED fabrication on foil and, specifically, picosecond laser ablation of PEDOT:PSS on multilayered barrier/foil or metal grids aimed as a synthetic alternative to inorganic transparent conductive electrodes. Key requirements include: (a) the complete removal of PEDOT layers without residue, (b) the complete absence of surface contamination from redeposited laser debris to avoid short circuiting and (c) no loss in performance of from laser exposure. We will demonstrate that with careful optimisation and appropriate choice of ultrafast laser, the above criteria can be fulfilled. A suitable process window exists resulting in clean laser structuring without damage to the underlying heat sensitive barrier layers whilst also containing laser debris. A low temperature ablation most likely proceeds via a stress-assisted (film fracture and ejection) process as opposed to vaporisation or other phase change commonly encountered with longer pulse lasers.

  11. Process for recovering 4,4 prime dihydroxydiphenyl sulfone from an isomer mixture

    SciTech Connect

    Zemlanicky, F.; Cooker, B.

    1991-03-19

    This patent describes a process for the recovery of 4,4{prime}-bisphenol sulfone from an isomer mixture comprising 4,4{prime}-bisphenol sulfone and 2,4{prime}-bisphenol sulfone. It comprises dissolving the isomer mixture in a basic aqueous solution comprising about one mole of base per mole of the mixture of 4,4{prime}-bisphenol sulfone and 2,4{prime}-bisphenol sulfone to form a basic isomer solution and adding acid to the isomer solution in an amount of from about 0.85 to 0.95 mole per mole of the 4,4{prime}-bisphenol sulfone wherein the acid is added in an amount sufficient to cause selective precipitation of crystals of 4,4{prime}-bisphenol sulfone yet in an amount less than sufficient to neutralize the isomer solution and removing the crystals of 4,4{prime}-bisphenol from the aqueous solution.

  12. Arabidopsis nonhost resistance gene PSS1 confers immunity against an oomycete and a fungal pathogen but not a bacterial pathogen that cause diseases in soybean

    PubMed Central

    2012-01-01

    Background Nonhost resistance (NHR) provides immunity to all members of a plant species against all isolates of a microorganism that is pathogenic to other plant species. Three Arabidopsis thaliana PEN (penetration deficient) genes, PEN1, 2 and 3 have been shown to provide NHR against the barley pathogen Blumeria graminis f. sp. hordei at the prehaustorial level. Arabidopsis pen1-1 mutant lacking the PEN1 gene is penetrated by the hemibiotrophic oomycete pathogen Phytophthora sojae, the causal organism of the root and stem rot disease in soybean. We investigated if there is any novel nonhost resistance mechanism in Arabidopsis against the soybean pathogen, P. sojae. Results The P.sojaesusceptible (pss) 1 mutant was identified by screening a mutant population created in the Arabidopsis pen1-1 mutant that lacks penetration resistance against the non adapted barley biotrophic fungal pathogen, Blumeria graminis f. sp. hordei. Segregation data suggested that PEN1 is not epistatic to PSS1. Responses of pss1 and pen1-1 to P. sojae invasion were distinct and suggest that PSS1 may act at both pre- and post-haustorial levels, while PEN1 acts at the pre-haustorial level against this soybean pathogen. Therefore, PSS1 encodes a new form of nonhost resistance. The pss1 mutant is also infected by the necrotrophic fungal pathogen, Fusarium virguliforme, which causes sudden death syndrome in soybean. Thus, a common NHR mechanism is operative in Arabidopsis against both hemibiotrophic oomycetes and necrotrophic fungal pathogens that are pathogenic to soybean. However, PSS1 does not play any role in immunity against the bacterial pathogen, Pseudomonas syringae pv. glycinea, that causes bacterial blight in soybean. We mapped PSS1 to a region very close to the southern telomere of chromosome 3 that carries no known disease resistance genes. Conclusions The study revealed that Arabidopsis PSS1 is a novel nonhost resistance gene that confers a new form of nonhost resistance against both

  13. Isotopic Measurements of Organic Sulfonates From The Murchison Meteorite

    NASA Technical Reports Server (NTRS)

    Cooper, G. W.; Chang, S.; DeVincenzi, Donald L. (Technical Monitor)

    1995-01-01

    Organic sulfonates and phosphonates have been extracted from the Murchison meteorite for stable isotope measurements. Preliminary stable isotope measurements of individual alkyl sulfonates, R-SO3H (R=C(sub n)H(sub 2n+l)), are shown. These compounds were found in aqueous extracts of Murchison. Both groups show trends similar to other homologous series of organic compounds indigenous to Murchison. Molecular abundances decrease with increasing carbon number, and all possible isomers at each carbon number (through C-4) are present. Carbon isotope measurements of the sulfonates show a decrease in the C-13/C-12 ratio with increasing carbon number. The overall objectives of this project are to obtain dime element carbon, hydrogen, and sulfur - intramolecular isotopic analyses of individual sulfonates, and isotopic measurement of carbon and hydrogen of the phosphonates as a group. The Murchison meteorite is the best characterized carbonaceous chondrite with respect to organic chemistry. The finding of organic sulfonates and phosphonates in Murchison is of interest because they are the first well-characterized series of sulfur and phosphorus containing organic compounds found in meteorites. Also, meteorites, comets, and interplanetary dust particles may have been involved in chemical evolution on the early Earth. Because of the critical role of organic phosphorus and sulfur in all living systems, it is particularly interesting to see examples of abiotic syntheses of these classes of compounds. The study of the isotopic composition of the sulfonates and phosphonates can yield insight into their possible interstellar origin as well as their mechanisms of synthesis in the early solar system. Previous isotopic analyses of other classes of organic compounds indigenous to meteorites, e.g., amino acids, carboxylic acids, and hydrocarbons indicate the possibility that interstellar molecules were incorporated into meteorite parent bodies. In these compounds the ratios of heavy to

  14. A Novel and Facile One-Pot Solvothermal Synthesis of PEDOT-PSS/Ni-Mn-Co-O Hybrid as an Advanced Supercapacitor Electrode Material.

    PubMed

    Yin, Chengjie; Yang, Chunming; Jiang, Min; Deng, Cuifen; Yang, Lishan; Li, Junhua; Qian, Dong

    2016-02-01

    In this work, a novel and facile one-pot method has been developed for the synthesis of a hybrid consisting of Ni-Mn-Co ternary oxide and poly(3,4-ethylenedioxythiophene)-polystyrenesulfonate (PEDOT-PSS/NMCO) with a hierarchical three-dimensional net structure via a solvothermal-coprecipitation coupled with oxidative polymerization route. Apart from the achievement of polymerization, coprecipitation, and solvothermal in one pot, the hydroxyl (OH(-)) ions generated from the oxidative polymerization of organic monomer by neutral KMnO4 solution were skillfully employed as precipitants for metal ions. As compared with the PEDOT-PSS/Ni-Mn binary oxide, PEDOT-PSS/Co-Mn binary oxide, and PEDOT-PSS/MnO2, PEDOT-PSS1.5/NMCO exhibits overwhelmingly superior supercapacitive performance, more specifically, a high specific capacitance of 1234.5 F g(-1) at a current density of 1 A g(-1), a good capacitance retention of 83.7% at a high current density of 5 A g(-1) after 1000 cycles, an energy density of 51.9 W h kg(-1) at a power density of 275 W kg(-1), and an energy density of 21.4 W h kg(-1) at an extremely elevated power density of 5500 W kg(-1). Noticeably, the energy density and power density of PEDOT-PSS/NMCO are by far higher than those of the existing analogues recently reported. The exceptional performance of PEDOT-PSS/NMCO benefits from its unique mesoporous architecture, which could provide a larger reaction surface area, faster ion and electron transfer ability, and good structural stability. The desirable integrated performance enables the multicomponent composite to be a promising electrode material for energy storage applications. PMID:26794146

  15. Improvement of the SiOx passivation layer for high-efficiency Si/PEDOT:PSS heterojunction solar cells.

    PubMed

    Sheng, Jiang; Fan, Ke; Wang, Dan; Han, Can; Fang, Junfeng; Gao, Pingqi; Ye, Jichun

    2014-09-24

    Interfacial properties currently hinder the performance of Si/organic heterojunction solar cells for an alternative to high-efficiency and low-cost photovoltaics. Here, we present a simple and repeatable wet oxidation method for developing the surface passivation layer, SiOx, on the Si surface for the fabrication of high-efficiency Si/poly(3,4-ethylene-dioxythiophene):polystyrenesulfonate (PEDOT:PSS) heterojunction solar cells. The uniform and dense SiOx thin layer introduced by the oxidizing aqueous solution of H2O2 or HNO3 provided the better surface passivation and stronger wettability of the Si surface, compared to those in the native oxide case. These two types of progress helped create a lower defect density at the Si/PEDOT:PSS interface and thus a high-quality p-n junction with a lower interface recombination velocity. As a result, the HNO3-oxidized device displayed better performance with a power conversion efficiency (PCE) of 11%, representing a 28.96% enhancement from the PCE of 8.53% in the native oxide case. The effects on the performance of the Si/PEDOT:PSS hybrid solar cells of the wet oxidation treatment procedure, including the differences in surface roughness and wettability of the Si substrate, the quality and thickness of the SiOx, etc., were explored extensively. Such a simple and controllable oxidizing treatment could be an effective way to promote the interfacial properties that are an important cornerstone for more efficient Si/organic hybrid solar cells.

  16. Covalent bonding of YIGSR and RGD to PEDOT/PSS/MWCNT-COOH composite material to improve the neural interface

    NASA Astrophysics Data System (ADS)

    Wang, Kun; Tang, Rong-Yu; Zhao, Xiao-Bo; Li, Jun-Jie; Lang, Yi-Ran; Jiang, Xiao-Xia; Sun, Hong-Ji; Lin, Qiu-Xia; Wang, Chang-Yong

    2015-11-01

    The development of coating materials for neural interfaces has been a pursued to improve the electrical, mechanical and biological performances. For these goals, a bioactive coating was developed in this work featuring a poly(3,4-ethylenedioxythiophene) (PEDOT)/carbon nanotube (CNT) composite and covalently bonded YIGSR and RGD. Its biological effect and electrical characteristics were assessed in vivo on microwire arrays (MWA). The coated electrodes exhibited a significantly higher charge storage capacity (CSC) and lower electrochemical impedance at 1 kHz which are desired to improve the stimulating and recording performances, respectively. Acute neural recording experiments revealed that coated MWA possess a higher signal/noise ratio capturing spikes undetected by uncoated electrodes. Moreover, coated MWA possessed more active sites and single units, and the noise floor of coated electrodes was lower than that of uncoated electrodes. There is little information in the literature concerning the chronic performance of bioactively modified neural interfaces in vivo. Therefore in this work, chronic in vivo tests were conducted and the PEDOT/PSS/MWCNT-polypeptide coated arrays exhibited excellent performances with the highest mean maximal amplitude from day 4 to day 12 during which the acute response severely compromised the performance of the electrodes. In brief, we developed a simple method of covalently bonding YIGSR and RGD to a PEDOT/PSS/MWCNT-COOH composite improving both the biocompatibility and electrical performance of the neural interface. Our findings suggest that YIGSR and RGD modified PEDOT/PSS/MWCNT is a promising bioactivated composite coating for neural recording and stimulating.

  17. Covalent bonding of YIGSR and RGD to PEDOT/PSS/MWCNT-COOH composite material to improve the neural interface.

    PubMed

    Wang, Kun; Tang, Rong-Yu; Zhao, Xiao-Bo; Li, Jun-Jie; Lang, Yi-Ran; Jiang, Xiao-Xia; Sun, Hong-Ji; Lin, Qiu-Xia; Wang, Chang-Yong

    2015-11-28

    The development of coating materials for neural interfaces has been a pursued to improve the electrical, mechanical and biological performances. For these goals, a bioactive coating was developed in this work featuring a poly(3,4-ethylenedioxythiophene) (PEDOT)/carbon nanotube (CNT) composite and covalently bonded YIGSR and RGD. Its biological effect and electrical characteristics were assessed in vivo on microwire arrays (MWA). The coated electrodes exhibited a significantly higher charge storage capacity (CSC) and lower electrochemical impedance at 1 kHz which are desired to improve the stimulating and recording performances, respectively. Acute neural recording experiments revealed that coated MWA possess a higher signal/noise ratio capturing spikes undetected by uncoated electrodes. Moreover, coated MWA possessed more active sites and single units, and the noise floor of coated electrodes was lower than that of uncoated electrodes. There is little information in the literature concerning the chronic performance of bioactively modified neural interfaces in vivo. Therefore in this work, chronic in vivo tests were conducted and the PEDOT/PSS/MWCNT-polypeptide coated arrays exhibited excellent performances with the highest mean maximal amplitude from day 4 to day 12 during which the acute response severely compromised the performance of the electrodes. In brief, we developed a simple method of covalently bonding YIGSR and RGD to a PEDOT/PSS/MWCNT-COOH composite improving both the biocompatibility and electrical performance of the neural interface. Our findings suggest that YIGSR and RGD modified PEDOT/PSS/MWCNT is a promising bioactivated composite coating for neural recording and stimulating.

  18. Preparation of allenic sulfones and allenes from the selenosulfonation of acetylenes

    SciTech Connect

    Back, T.G.; Krishna, M.V.; Muralidharan, K.R. )

    1989-08-18

    {beta}-(phenylseleno)vinyl sulfones 2 are readily obtained from the free-radical selenosulfonation of acetylenes. Compounds 2 isomerize to allyl sulfones 4 under base-catalyzed conditions in nearly quantitative yield, with high stereoselectivity favoring the Z configuration. Allyl sulfones 4 afford generally high yields of allenic sulfones 1 when subjected to oxidation with m-chloroperbenzoic acid or tert-butyl hydroperoxide, followed by selenoxide syn-elimination. The sulfone-stabilized anion intermediates in the isomerizations of 2 to 4 can be alkylated, deuterated, or silylated in the {alpha}-position prior to oxidation, providing allenic sulfones with an additional {alpha}-substituent. In some cases, spontaneous elimination of the phenylseleno group occurred, producing the allenic sulfone without the need for an oxidation step. Desulfonylation of allyl sulfones 4f, 4c, and 25 with sodium amalgam afforded vinyl selenides that were converted to allenes in moderate to good yields by oxidation-elimination. The copper-catalyzed coupling of allyl sulfones 4 with Grignard reagents comprises an alternative route to vinyl selenide precursors of allenes. These procedures permit the synthesis of various {alpha}- and {gamma}-substituted allenic sulfones and allenes from acetylenes.

  19. Regioselective synthesis of chiral dimethyl-bis(ethylenedithio)tetrathiafulvalene sulfones

    PubMed Central

    Pop, Flavia

    2015-01-01

    Summary Enantiopure (R,R) and (S,S)-dimethyl-bis(ethylenedithio)tetrathiafulvalene monosulfones have been synthesized by the aerial oxidation of the chiral dithiolates generated from the propionitrile-protected precursors. Both enantiomers crystallize in the orthorhombic chiral space group P212121. They show a boat-type conformation of the TTF moiety, a rather rigid dithiin sulfone ring and the methyl groups in a bisequatorial conformation. Cyclic voltammetry measurements indicate fully reversible oxidation in radical cation and dication species. PMID:26199666

  20. The phase behavior of simple salt-tolerant sulfonates

    SciTech Connect

    Barakat, Y.; Fortney, L.N.; LaLanne-Cassou, C.; Schecter, R.S.; Wade, W.H.; Weerasooriya, U.; Yiv, S.

    1983-12-01

    Alkane and ..cap alpha..-olefin sulfonates can be used to produce optimal microemulsion formulations having very high salinity tolerance (including divalent ion) while maintaining large solubilization parameters and low interfacial tensions (IFT's). Such molecules require elevated temperatures or higher alcohol concentrations to suppress liquid crystal formation. As in other species, solubilization is inversely related to width of the threephase regime, and IFT and solubilization are strongly coupled.

  1. Ultrasound assisted regioselective sulfonation of aromatic compounds with sulfuric acid.

    PubMed

    Qureshi, Ziyauddin S; Deshmukh, Krishna M; Jagtap, Sachin R; Nandurkar, Nitin S; Bhanage, Bhalchandra M

    2009-03-01

    A simple and convenient methodology for selective sulfonation of aromatic compounds using sulfuric acid under sonication is described. The present methodology shows a considerable enhancement in the reaction rate along with improved selectivity compared with the reactions performed under silent conditions. The effect of various parameters such as agitation speed, sulfuric acid concentration, and temperature on reaction system have been investigated and are explained on the basis of ultrasonically generated cavitational effects. PMID:19014895

  2. Formulation of soluble oils with synthetic and petroleum sulfonates

    SciTech Connect

    Eckard, A.; Riff, I.; Weaver, J.

    1997-06-01

    Metalworking fluids for metal removal are formulated to provide cooling, lubrication, and rust protection when cutting and machining metals. There are basically four types of cutting fluids: straight oils, synthetics, semisynthetic fluids and soluble oils. The last type is the most widely used for metal removal operations such as cutting, drilling and grinding. Soluble oils used for metalworking operations are normally the oil-in-water type, with oil as the internal phase and water as the external phase. The soluble oils can have rather complex compositions, usually containing two or more emulsifiers and coupling agents, as well as additives to provide rust inhibition, lubricity, detergency, resistance to bacterial attack and foam control. The dominant emulsifier in a soluble oil is usually sodium sulfonate which also has the secondary benefit of being a rust inhibitor. Soluble oil emulsions based on petroleum or synthetic sulfonates have been found to improve lubrication and cleaning of metal parts and equipment. As has been done previously, a series of emulsification studies were conducted using petroleum and synthetic sulfonates. Emulsifier level, coemulsifiers and minor formulation adjustments were made to optimize each system. This study was made using naphthenic oil basestock. Formulations were evaluated using criteria including concentrate stability, hard and soft water emulsion stability, emulsibility, foaming tendency and response to defoamers, antirust properties and cost effectiveness of individual formulations. The results of these evaluations are presented in the present paper.

  3. Electric current-producing device having sulfone-based electrolyte

    SciTech Connect

    Angell, Charles Austen; Sun, Xiao-Guang

    2010-11-16

    Electrolytic solvents and applications of such solvents including electric current-producing devices. For example, a solvent can include a sulfone compound of R1--SO2--R2, with R1 being an alkyl group and R2 a partially oxygenated alkyl group, to exhibit high chemical and thermal stability and high oxidation resistance. For another example, a battery can include, between an anode and a cathode, an electrolyte which includes ionic electrolyte salts and a non-aqueous electrolyte solvent which includes a non-symmetrical, non-cyclic sulfone. The sulfone has a formula of R1--SO2--R2, wherein R1 is a linear or branched alkyl or partially or fully fluorinated linear or branched alkyl group having 1 to 7 carbon atoms, and R2 is a linear or branched or partially or fully fluorinated linear or branched oxygen containing alkyl group having 1 to 7 carbon atoms. The electrolyte can include an electrolyte co-solvent and an electrolyte additive for protective layer formation.

  4. Composite plasma polymerized sulfonated polystyrene membrane for PEMFC

    SciTech Connect

    Nath, Bhabesh Kumar; Khan, Aziz; Chutia, Joyanti

    2015-10-15

    Highlights: • Methyl methane sulfonate (MMS) is used as the sulfonating agent. • The proton conductivity of the membrane is found to be 0.141 S cm{sup −1}. • Power density of fuel cell with styrene/MMS membrane is 0.5 W cm{sup −2}. • The membrane exhibits thermal stability up to 140 °C. - Abstract: This work presents the introduction of an organic compound methyl methane sulfonate (MMS) for the first time in fabrication of polystyrene based proton exchange membrane (PEM) by plasma polymerization process. The membrane is fabricated by co-polymerizing styrene and MMS in capacitively coupled continuous RF plasma. The chemical composition of the plasma polymerized polymer membrane is investigated using Fourier Transform Infrared Spectroscopy which reveals the formation of composite structure of styrene and MMS. The surface morphology studied using AFM and SEM depicts the effect of higher partial pressure of MMS on surface topography of the membrane. The proton transport property of the membrane studied using electrochemical impedance spectroscopy shows the achievement of maximum proton conductivity of 0.141 S cm{sup −1} which is comparable to Nafion 117 membrane. Fuel cell performance test of the synthesized membrane shows a maximum power density of 500 mW cm{sup −2} and current density of 0.62 A cm{sup −2} at 0.6 V.

  5. Amperometric urea biosensors based on sulfonated graphene/polyaniline nanocomposite

    PubMed Central

    Das, Gautam; Yoon, Hyon Hee

    2015-01-01

    An electrochemical biosensor based on sulfonated graphene/polyaniline nanocomposite was developed for urea analysis. Oxidative polymerization of aniline in the presence of sulfonated graphene oxide was carried out by electrochemical methods in an aqueous environment. The structural properties of the nanocomposite were characterized by Fourier-transform infrared, Raman spectroscopy, X-ray photoelectron spectroscopy, and scanning electron microscopy techniques. The urease enzyme-immobilized sulfonated graphene/polyaniline nanocomposite film showed impressive performance in the electroanalytical detection of urea with a detection limit of 0.050 mM and a sensitivity of 0.85 (μA · cm−2·mM−1. The biosensor achieved a broad linear range of detection (0.12–12.3 mM) with a notable response time of approximately 5 seconds. Moreover, the fabricated biosensor retained 81% of its initial activity (based on sensitivity) after 15 days of storage at 4°C. The ease of fabrication coupled with the low cost and good electrochemical performance of this system holds potential for the development of solid-state biosensors for urea detection. PMID:26346240

  6. Amperometric urea biosensors based on sulfonated graphene/polyaniline nanocomposite.

    PubMed

    Das, Gautam; Yoon, Hyon Hee

    2015-01-01

    An electrochemical biosensor based on sulfonated graphene/polyaniline nanocomposite was developed for urea analysis. Oxidative polymerization of aniline in the presence of sulfonated graphene oxide was carried out by electrochemical methods in an aqueous environment. The structural properties of the nanocomposite were characterized by Fourier-transform infrared, Raman spectroscopy, X-ray photoelectron spectroscopy, and scanning electron microscopy techniques. The urease enzyme-immobilized sulfonated graphene/polyaniline nanocomposite film showed impressive performance in the electroanalytical detection of urea with a detection limit of 0.050 mM and a sensitivity of 0.85 (μA · cm(-2)·mM(-1). The biosensor achieved a broad linear range of detection (0.12-12.3 mM) with a notable response time of approximately 5 seconds. Moreover, the fabricated biosensor retained 81% of its initial activity (based on sensitivity) after 15 days of storage at 4°C. The ease of fabrication coupled with the low cost and good electrochemical performance of this system holds potential for the development of solid-state biosensors for urea detection.

  7. Effect of additives on the performance and morphology of sulfonated copoly (phthalazinone biphenyl ether sulfone) composite nanofiltration membranes☆

    NASA Astrophysics Data System (ADS)

    Guan, Shanshan; Zhang, Shouhai; Liu, Peng; Zhang, Guozhen; Jian, Xigao

    2014-03-01

    Sulfonated copoly (phthalazinone biphenyl ether sulfone) (SPPBES) composite nanofiltration membranes were fabricated by adding low molecular weight additives into SPPBES coating solutions during a dip coating process. Three selected additives: glycol, glycerol and hydroquinone were used in this work. The effect of additives on the membrane performance was studied and discussed in terms of rejection and permeation flux. Among all the composite membranes, the membrane prepared with glycol as an additive achieved the highest Na2SO4 rejection, and the membrane fabricated with glycerol as an additive exhibited the highest flux. The salts rejection of SPPBES composite membranes increased in the following order MgCl2 < NaCl ≤ MgSO4 < Na2SO4. The morphologies of the SPPBES composite membranes were characterized by SEM, it was found that the membrane prepared with hydroquinone showed a rough membrane surface. Composite membrane fabricated with glycol or glycerol as the additive showed very good chemical stability.

  8. Proton Conduction in Sulfonated Organic-Inorganic Hybrid Monoliths with Hierarchical Pore Structure.

    PubMed

    von der Lehr, Martin; Seidler, Christopher F; Taffa, Dereje H; Wark, Michael; Smarsly, Bernd M; Marschall, Roland

    2016-09-28

    Porous organic-inorganic hybrid monoliths with hierarchical porosity exhibiting macro- and mesopores are prepared via sol-gel process under variation of the mesopore size. Organic moieties in the pore walls are incorporated by substituting up to 10% of the silicon precursor tetramethylorthosilicate with bisilylated benzene molecules. After functionalization with sulfonic acid groups, the resulting sulfonated hybrid monoliths featuring a bimodal pore structure are investigated regarding proton conduction depending on temperature and relative humidity. The hierarchical pore system and controlled mesopore design turn out to be crucial for sulfonation and proton conduction. These sulfonated hybrid hierarchical monoliths containing only 10% organic precursor exhibit higher proton conduction at different relative humidities than sulfonated periodic mesoporous organosilica made of 100% bisilylated precursors exhibiting solely mesopores, even with a lower concentration of sulfonic acid groups. PMID:27598017

  9. Proton Conduction in Sulfonated Organic-Inorganic Hybrid Monoliths with Hierarchical Pore Structure.

    PubMed

    von der Lehr, Martin; Seidler, Christopher F; Taffa, Dereje H; Wark, Michael; Smarsly, Bernd M; Marschall, Roland

    2016-09-28

    Porous organic-inorganic hybrid monoliths with hierarchical porosity exhibiting macro- and mesopores are prepared via sol-gel process under variation of the mesopore size. Organic moieties in the pore walls are incorporated by substituting up to 10% of the silicon precursor tetramethylorthosilicate with bisilylated benzene molecules. After functionalization with sulfonic acid groups, the resulting sulfonated hybrid monoliths featuring a bimodal pore structure are investigated regarding proton conduction depending on temperature and relative humidity. The hierarchical pore system and controlled mesopore design turn out to be crucial for sulfonation and proton conduction. These sulfonated hybrid hierarchical monoliths containing only 10% organic precursor exhibit higher proton conduction at different relative humidities than sulfonated periodic mesoporous organosilica made of 100% bisilylated precursors exhibiting solely mesopores, even with a lower concentration of sulfonic acid groups.

  10. Poly(ether sulfone) as a negative resist for electron beam lithography

    NASA Astrophysics Data System (ADS)

    Bryce, R. M.; Freeman, M. R.; Aktary, M.

    2007-05-01

    The sulfone containing polymer poly(butene sulfone) has long been used as positive electron beam resist due to the high scission rate of sulfone under electron irradiation. The authors demonstrate that poly(ether sulfone) acts as a high resolution negative electron beam resist which displays good chemical and dry-etch resistance. The electron beam exposure sensitivity at 10kV was found to be approximately 230μC/cm2 for poly(ether sulfone), roughly 2.3 times that of poly(methyl methacrylate). As poly(ether sulfone) is a robust engineering polymer that can withstand etching this polymer is a suitable mask material and has properties of interest for direct incorporation in devices.

  11. High-Performance Flexible All-Solid-State Supercapacitor from Large Free-Standing Graphene-PEDOT/PSS Films

    PubMed Central

    Liu, Yuqing; Weng, Bo; Razal, Joselito M.; Xu, Qun; Zhao, Chen; Hou, Yuyang; Seyedin, Shayan; Jalili, Rouhollah; Wallace, Gordon G.; Chen, Jun

    2015-01-01

    Although great attention has been paid to wearable electronic devices in recent years, flexible lightweight batteries or supercapacitors with high performance are still not readily available due to the limitations of the flexible electrode inventory. In this work, highly flexible, bendable and conductive rGO-PEDOT/PSS films were prepared using a simple bar-coating method. The assembled device using rGO-PEDOT/PSS electrode could be bent and rolled up without any decrease in electrochemical performance. A relatively high areal capacitance of 448 mF cm−2 was achieved at a scan rate of 10 mV s−1 using the composite electrode with a high mass loading (8.49 mg cm−2), indicating the potential to be used in practical applications. To demonstrate this applicability, a roll-up supercapacitor device was constructed, which illustrated the operation of a green LED light for 20 seconds when fully charged. PMID:26586106

  12. Heterojunction solar cell fabricated by spin-coating of a CNT/PEDOT:PSS heteroemitter on top of a crystalline silicon absorber

    NASA Astrophysics Data System (ADS)

    Neitzert, Heinz-Christoph; Schwertheim, Stefan; Meusinger, Katrin; Leinhos, Marcel; Fahrner, Wolfgang R.

    2009-05-01

    Crystalline silicon / organic thin film heterojunction based solar cells have been realized using spin-coating deposition. Devices with different organic films, all based on PEDOT:PSS, which in some cases have been mixed with double-walled or multi-walled carbon nanotubes, have been compared. Highest conversion efficiencies have been obtained either with a highly conductive PEDOT:PSS emitter withut nanotubes or with a nanocomposite emitter consisting of low conductive PEDOT:PSS emitter mixed with multi-walled carbon nanotubes. Using the nanocomposite emitter, rather high values for the solar cell shunt resistances have been obtained without any etching procedure in order to improve the lateral current confinement. A comparison with a Schottky diode, realized as reference device by the evaporation of the top metal contact directly on top of the crystalline silicon substrate, showed that the heterodiode characteristics was not dominated by leakage current paths and short circuits through the organic layer.

  13. Impedimetric Sensing Proprieties of ITO Electrodes Functionalized with PEDOT:PSS/Azo-Calix[4]Arene for the Detection of Al3+ Ions Under Light Excitation

    NASA Astrophysics Data System (ADS)

    Echabaane, M.; Rouis, A.; Mahjoub, M. A.; Bonnamour, I.; Ben Ouada, H.

    2016-08-01

    This study describes an investigation of the sensitivity of the azo-calix[4]arene/poly(3,4-ethylenedioxythiophene)/poly-(styrenesulfonate) (PEDOT:PSS) thin film deposited on the indium tin oxide (ITO) electrode surface toward aluminum ions (Al3+) under light excitation. Thin films were deposited by the spin-coating technique. Adhesion of these films to the ITO surface was highlighted by performing contact angle measurements. Then, interfaces of the azo-calix[4]arene/PEDOT:PSS thin film were characterized by impedance measurements using electrochemical impedance spectroscopy. Obtained impedance spectra were fitted using an equivalent circuit. Finally, evolutions of the different components of this circuit were studied. These evolutions show that the sensitivity of the azo-calix[4]arene/PEDOT:PSS/ITO electrode is remarkably improved under illumination.

  14. Solution synthesis of telluride-based nano-barbell structures coated with PEDOT:PSS for spray-printed thermoelectric generators

    NASA Astrophysics Data System (ADS)

    Bae, Eun Jin; Kang, Young Hun; Jang, Kwang-Suk; Lee, Changjin; Cho, Song Yun

    2016-05-01

    Solution-processable telluride-based heterostructures coated with poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (Te-Bi2Te3/PEDOT:PSS) were synthesized through a solution-phase reaction at low temperatures. The water-based synthesis yielded PEDOT:PSS-coated Te-Bi2Te3 nano-barbell structures with a high Seebeck coefficient that can be stably dispersed in water. These hybrid solutions were deposited onto a substrate by the spray-printing method to prepare thermoelectric generators. The thermoelectric properties of the Te-Bi2Te3/PEDOT:PSS hybrid films were significantly enhanced by a simple acid treatment due to the increased electrical conductivity, and the power factor of those materials can be effectively tuned over a wide range depending on the acid concentration of the treatment. The power factors of the synthesized Te-Bi2Te3/PEDOT:PSS hybrids were optimized to 60.05 μW m-1 K-2 with a Seebeck coefficient of 93.63 μV K-1 and an electrical conductivity of 69.99 S cm-1. The flexible thermoelectric generator fabricated by spray-printing Te-Bi2Te3/PEDOT:PSS hybrid solutions showed an open-circuit voltage of 1.54 mV with six legs at ΔT = 10 °C. This approach presents the potential for realizing printing-processable hybrid thermoelectric materials for application in flexible thermoelectric generators.Solution-processable telluride-based heterostructures coated with poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (Te-Bi2Te3/PEDOT:PSS) were synthesized through a solution-phase reaction at low temperatures. The water-based synthesis yielded PEDOT:PSS-coated Te-Bi2Te3 nano-barbell structures with a high Seebeck coefficient that can be stably dispersed in water. These hybrid solutions were deposited onto a substrate by the spray-printing method to prepare thermoelectric generators. The thermoelectric properties of the Te-Bi2Te3/PEDOT:PSS hybrid films were significantly enhanced by a simple acid treatment due to the increased electrical conductivity, and

  15. Sulfonates: A novel class of organic sulfur compounds in marine sediments

    NASA Astrophysics Data System (ADS)

    Vairavamurthy, Appathurai; Zhou, Weiqing; Eglinton, Timothy; Manowitz, Bernard

    1994-11-01

    X-ray absorption near-edge structure spectroscopy (XANES) used to measure sulfur speciation in a variety of organic-rich marine sediments has established sulfonates as a novel and major component of sedimentary organic sulfur. The origins of sulfonates in sediments are not clear, although both biological and geochemical mechanisms are possible. The accumulation of oxidized sulfonate sulfur in reducing marine sediments was not known previously; hence, a new perspective in sulfur geochemistry is established. The biogeochemical implications of the presence of sulfonates in marine sediments are discussed.

  16. 3D conductive nanocomposite scaffold for bone tissue engineering

    PubMed Central

    Shahini, Aref; Yazdimamaghani, Mostafa; Walker, Kenneth J; Eastman, Margaret A; Hatami-Marbini, Hamed; Smith, Brenda J; Ricci, John L; Madihally, Sundar V; Vashaee, Daryoosh; Tayebi, Lobat

    2014-01-01

    Bone healing can be significantly expedited by applying electrical stimuli in the injured region. Therefore, a three-dimensional (3D) ceramic conductive tissue engineering scaffold for large bone defects that can locally deliver the electrical stimuli is highly desired. In the present study, 3D conductive scaffolds were prepared by employing a biocompatible conductive polymer, ie, poly(3,4-ethylenedioxythiophene) poly(4-styrene sulfonate) (PEDOT:PSS), in the optimized nanocomposite of gelatin and bioactive glass. For in vitro analysis, adult human mesenchymal stem cells were seeded in the scaffolds. Material characterizations using hydrogen-1 nuclear magnetic resonance, in vitro degradation, as well as thermal and mechanical analysis showed that incorporation of PEDOT:PSS increased the physiochemical stability of the composite, resulting in improved mechanical properties and biodegradation resistance. The outcomes indicate that PEDOT:PSS and polypeptide chains have close interaction, most likely by forming salt bridges between arginine side chains and sulfonate groups. The morphology of the scaffolds and cultured human mesenchymal stem cells were observed and analyzed via scanning electron microscope, micro-computed tomography, and confocal fluorescent microscope. Increasing the concentration of the conductive polymer in the scaffold enhanced the cell viability, indicating the improved microstructure of the scaffolds or boosted electrical signaling among cells. These results show that these conductive scaffolds are not only structurally more favorable for bone tissue engineering, but also can be a step forward in combining the tissue engineering techniques with the method of enhancing the bone healing by electrical stimuli. PMID:24399874

  17. Sulfone/Ester Polymers Containing Pendent Ethynyl Groups

    NASA Technical Reports Server (NTRS)

    Hergenrother, P. M.; Jensen, B. J.

    1986-01-01

    Two processes make high-performance polymers resistant to solvents, without compromising mechanical characteristics. Polymers show improved solvent resistance while retaining high toughness, thermoformability, and mechanical performance. Multistep process involves conversion of pendent bromo group to ethynyl group, while direct process involves reacting hydroxy-terminated sulfone oligomers or polymers with stoichiometric amount of 5-(4-ethynylphenoxy) isophthaloyl chloride. Applications for new polymers include adhesives, composite resin matrices, moldings, ultrafiltration membranes, protective coatings, and such electrical insulators as thin films for microelectronic circuitry.

  18. The Palladium-Catalyzed Trifluoromethylation of Vinyl Sulfonates

    PubMed Central

    Cho, Eun Jin; Buchwald, Stephen L.

    2011-01-01

    A method for the palladium-catalyzed trifluoromethylation of cyclohexenyl sulfonates has been developed. Various cyclohexenyl triflates and nonaflates underwent trifluoromethylation under mild reaction conditions using a catalyst system composed of Pd(dba)2 or [(allyl)PdCl]2 and the monodentate biaryl phosphine ligand tBuXPhos. The trifluoromethyl anion (CF3−) or its equivalent for the process was generated in situ from TMSCF3 in combination with KF or TESCF3 in combintion with RbF. PMID:22111687

  19. Bis(3-amino-phen-yl) sulfone acetonitrile solvate.

    PubMed

    Yao, Wei; Li, Fang-Shi; Yu, Da-Sheng; Lu, Chui; Zhu, Jin-Na

    2008-05-21

    In the sulfone mol-ecule of the title compound, C(12)H(12)N(2)O(2)S·C(2)H(3)N, the two benzene rings are oriented at a dihedral angle of 80.69 (3)°. Weak intra-molecular C-H⋯O hydrogen bonds result in the formation of two five-membered rings, which both have envelope conformations. In the crystal structure, inter-molecular N-H⋯O hydrogen bonds link the mol-ecules.

  20. Study on the disparate transition behaviors of the electrical/physical properties in PEDOT:PSS film depending on solvent species under a follow-up solution-treatment process

    NASA Astrophysics Data System (ADS)

    Yun, Dong-Jin; Kim, Jung-Hwa; Kim, Seong Heon; Seol, Minsu; Yu, DaEun; Kwon, Hyukju; Ham, Yongnam; Chung, JaeGwan; Kim, Yongsu; Heo, Sung

    2016-04-01

    In most solution-processed organic devices, a poly(3,4-ethylenedioxythiophene) (PEDOT) polymerized with poly(4-styrenesulfonate) (PSS) film is inevitably affected by various conditions during the subsequent solution-coating processes. To investigate the effects of direct solvent exposure on the properties of PEDOT polymerized with PSS (PEDOT:PSS) films, photoemission spectroscopy-based analytical methods were used before and after solvent-coating processes. Our results clearly indicate that PEDOT:PSS films undergo a different transition mechanism depending on the solubility of the solvent in water. The water-miscible solvents induce the solvation of hydrophilic PSS chains. As a result, this process allows the solvent to diffuse into the PEDOT:PSS film, and a conformational change between PEDOT and PSS occurs. On the other hand, the water-immiscible organic solvents cause the partial adsorption of solvent molecules at the PE surface, which leads to changes in the surface properties, including work function. Based on our finding, we demonstrate that the energy-level alignments at the organic semiconductor/electrode interface for the PEDOT:PSS films can be controlled by simple solvent treatments.

  1. Rh(III)-catalyzed synthesis of sultones through C-H activation directed by a sulfonic acid group.

    PubMed

    Qi, Zisong; Wang, Mei; Li, Xingwei

    2014-09-01

    A new rhodium-catalyzed synthesis of sultones via the oxidative coupling of sulfonic acids with internal alkynes is described. The reaction proceeds via aryl C-H activation assisted by a sulfonic acid group.

  2. The role of MgBr2 to enhance the ionic conductivity of PVA/PEDOT:PSS polymer composite

    PubMed Central

    Sheha, Eslam M.; Nasr, Mona M.; El-Mansy, Mabrouk K.

    2014-01-01

    A solid polymer electrolyte system based on poly(vinyl alcohol) (PVA) and poly(3,4-Etylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) complexed with magnesium bromide (MgBr2) salt was prepared using solution cast technique. The ionic conductivity is observed to increase with increasing MgBr2 concentration. The maximum conductivity was found to be 9.89 × 10−6 S/cm for optimum polymer composite film (30 wt.% MgBr2) at room temperature. The increase in the conductivity is attributed to the increase in the number of ions as the salt concentration is increased. This has been proven by dielectric studies. The increase in conductivity is also attributable to the increase in the fraction of amorphous region in the electrolyte films as confirmed by their structural, thermal, electrical and optical properties. PMID:26199746

  3. Arylative Desulfonation of Diarylmethyl Phenyl Sulfone with Arenes Catalyzed by Scandium Triflate.

    PubMed

    Nambo, Masakazu; Ariki, Zachary T; Canseco-Gonzalez, Daniel; Beattie, D Dawson; Crudden, Cathleen M

    2016-05-20

    A scandium-triflate-catalyzed arylative desulfonation of diarylmethyl phenyl sulfones with arenes and heteroarenes was established. A variety of both sulfone and arene substrates were reacted to afford symmetric and nonsymmetric triarylmethanes in good yields. Further transformations of the resulting triarylmethanes and application to the concise synthesis of a bactericidal agent analogue were also demonstrated.

  4. Oil recovery method utilizing a dialkyl phenol polyethoxy alkyl sulfonate as a solubilizing co-surfactant

    SciTech Connect

    Dunn, N.G.; Hughes, J.W.; Kudchadker, M.V.

    1980-09-02

    The dialkylbenzene polyethoxy alkyl sulfonate is combined with a water soluble petroleum sulfonate surfactant to form an effective surfactant solution that is stable in high salinity environments. The surfactant solution is injected into an underground petroleum reservoir in order to recover crude oil therefrom.

  5. Arylative Desulfonation of Diarylmethyl Phenyl Sulfone with Arenes Catalyzed by Scandium Triflate.

    PubMed

    Nambo, Masakazu; Ariki, Zachary T; Canseco-Gonzalez, Daniel; Beattie, D Dawson; Crudden, Cathleen M

    2016-05-20

    A scandium-triflate-catalyzed arylative desulfonation of diarylmethyl phenyl sulfones with arenes and heteroarenes was established. A variety of both sulfone and arene substrates were reacted to afford symmetric and nonsymmetric triarylmethanes in good yields. Further transformations of the resulting triarylmethanes and application to the concise synthesis of a bactericidal agent analogue were also demonstrated. PMID:27124389

  6. 40 CFR 721.10045 - Diazotized substituted heteromonocycle coupled with naphthalene sulfonic acid derivative, nickel...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... coupled with naphthalene sulfonic acid derivative, nickel complex, alkaline salt (generic). 721.10045... derivative, nickel complex, alkaline salt (generic). (a) Chemical substance and significant new uses subject... heteromonocycle coupled with naphthalene sulfonic acid derivative, nickel complex, alkaline salt (PMN P-02-737)...

  7. 40 CFR 721.10045 - Diazotized substituted heteromonocycle coupled with naphthalene sulfonic acid derivative, nickel...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... coupled with naphthalene sulfonic acid derivative, nickel complex, alkaline salt (generic). 721.10045... derivative, nickel complex, alkaline salt (generic). (a) Chemical substance and significant new uses subject... heteromonocycle coupled with naphthalene sulfonic acid derivative, nickel complex, alkaline salt (PMN P-02-737)...

  8. 40 CFR 721.10045 - Diazotized substituted heteromonocycle coupled with naphthalene sulfonic acid derivative, nickel...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... coupled with naphthalene sulfonic acid derivative, nickel complex, alkaline salt (generic). 721.10045... derivative, nickel complex, alkaline salt (generic). (a) Chemical substance and significant new uses subject... heteromonocycle coupled with naphthalene sulfonic acid derivative, nickel complex, alkaline salt (PMN P-02-737)...

  9. 40 CFR 721.10045 - Diazotized substituted heteromonocycle coupled with naphthalene sulfonic acid derivative, nickel...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... coupled with naphthalene sulfonic acid derivative, nickel complex, alkaline salt (generic). 721.10045... derivative, nickel complex, alkaline salt (generic). (a) Chemical substance and significant new uses subject... heteromonocycle coupled with naphthalene sulfonic acid derivative, nickel complex, alkaline salt (PMN P-02-737)...

  10. 40 CFR 721.10045 - Diazotized substituted heteromonocycle coupled with naphthalene sulfonic acid derivative, nickel...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... coupled with naphthalene sulfonic acid derivative, nickel complex, alkaline salt (generic). 721.10045... derivative, nickel complex, alkaline salt (generic). (a) Chemical substance and significant new uses subject... heteromonocycle coupled with naphthalene sulfonic acid derivative, nickel complex, alkaline salt (PMN P-02-737)...

  11. Bis-sulfonic acid ionic liquids for the conversion of fructose to 5-hydroxymethyl-2-furfural.

    PubMed

    Sim, Sang Eun; Kwon, Sunjeong; Koo, Sangho

    2012-10-31

    Homogenous bis-sulfonic acid ionic liquids (1 mol equiv.) in DMSO (10 mol equiv.) at 100 °C efficiently mediated the conversion of D-fructose into 5-hydroxymethyl-2-furfural in 75% isolated yield, which was roughly a 10% increment compared to the case of the mono-sulfonic acid ionic liquids.

  12. Synthesis and Structure-Property Relationships of Poly(sulfone)s for Anion Exchange Membranes

    SciTech Connect

    Yan, JL; Moore, HD; Hibbs, MR; Hickner, MA

    2013-10-05

    Membranes based on cationic polymers that conduct anions are important for enabling alkaline membrane fuel cells and other solid-state electrochemical devices that operate at high pH. Anion exchange membranes with poly(arylene ether sulfone) backbones are demonstrated by two routes: chloromethylation of commercially available poly(sulfone)s or radical bromination of benzylmethyl moieties in poly(sulfone)s containing tetramethylbisphenol A monomer residues. Polymers with tethered trimethylbenzyl ammonium moieties resulted from conversion of the halomethyl groups by quaternization with trimethyl amine. The water uptake of the chloromethylated polymers was dependent on the type of poly(sulfone) backbone for a given IEC. Bisphenol A-based Udel (R) poly(sulfone) membranes swelled in water to a large extent while membranes from biphenol-based Radel (R) poly(sulfone), a stiffer backbone than Udel, only showed moderate water uptake. The water uptake of cationic poly(sulfone)s was further reduced by synthesizing tetramethylbisphenol A and 4,4-biphenol-containing poly(sulfone) copolymers where the ionic groups were clustered on the tetramethylbisphenol A residues. The conductivity of all samples scaled with the bulk water uptake. The hydration number of the membranes could be increased by casting membranes from the ionic form polymers versus converting the halomethyl form cast polymers to ionic form in the solid state. (c) 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2013, 51, 1790-1798, 2013

  13. Enantioselective transformation of Na2SO3 into allylic sulfonic acids under Pd catalysis.

    PubMed

    Liu, Wei; Zhao, Xiao-ming; Zhang, Hong-bo; Zhang, Liang

    2015-01-14

    Pd-catalyzed asymmetric allylic sulfonation of di-aryl-substituted allylic acetates with sodium sulfite (Na2SO3) in THF-H2O at room temperature was described. This method directly provided allylic sulfonic acids in up to excellent yield and enantioselectivity. PMID:25415622

  14. Colonic necrosis due to calcium polystyrene sulfonate (Kalimate) not suspended in sorbitol.

    PubMed

    Castillo-Cejas, María Dolores; de-Torres-Ramírez, Inés; Alonso-Cotoner, Carmen

    2013-04-01

    Cation-exchange resins are used in the management of hyperkalemia, particularly in patients with end-stage renal disease. These resins were associated with gastrointestinal tract lesions, especially sodium polystyrene sulfonate (Kayexalate) mixed with sorbitol. We present a case of colonic necrosis after the administration of calcium polystyrene sulfonate (Kalimate) not suspended in sorbitol.

  15. Calix[4]arene sulfonate as a template for forming fluorescent thiazole orange H-aggregates.

    PubMed

    Lau, Vivian; Heyne, Belinda

    2010-05-28

    The unexpected interaction between thiazole orange (TO) and calix[4]arene sulfonate is reported herein. H-Aggregates of TO switching on their fluorescence in solution are observed. Surprisingly, fluorescence enhancement is not linked to host-guest inclusion, but rather to calix[4]arene sulfonate serving as a template for several TO molecules.

  16. 40 CFR 721.10487 - Alkylbenzenes sulfonic acids, metal salts (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... salts (generic). 721.10487 Section 721.10487 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.10487 Alkylbenzenes sulfonic acids, metal salts (generic). (a) Chemical... as alkylbenzenes sulfonic acids, metal salts (PMNs P-04-599, P-04-600, P-04-605, and P-04-606)...

  17. Performance and Long-Term Stability of Pd/PSS and Pd/Al2O3 Membranes for Hydrogen Separation.

    PubMed

    Liguori, Simona; Iulianelli, Adolfo; Dalena, Francesco; Pinacci, Pietro; Drago, Francesca; Broglia, Maria; Huang, Yan; Basile, Angelo

    2014-03-06

    The present work is focused on the investigation of the performance and long-term stability of two composite palladium membranes under different operating conditions. One membrane (Pd/porous stainless steel (PSS)) is characterized by a ~10 µm-thick palladium layer on a porous stainless steel substrate, which is pretreated by means of surface modification and oxidation; the other membrane (Pd/Al2O3) is constituted by a ~7 µm-thick palladium layer on an asymmetric microporous Al2O3 substrate. The operating temperature and pressure ranges, used for studying the performance of these two kinds of membranes, are 350-450 °C and 200-800 kPa, respectively. The H2 permeances and the H2/N2 selectivities of both membranes were investigated and compared with literature data. At 400 °C and 200 kPa as pressure difference, Pd/PSS and Pd/Al2O3 membranes exhibited an H2/N2 ideal selectivity equal to 11700 and 6200, respectively, showing stability for 600 h. Thereafter, H2/N2 selectivity of both membranes progressively decreased and after around 2000 h, dropped dramatically to 55 and 310 for the Pd/PSS and Pd/Al2O3 membranes, respectively. As evidenced by Scanning Electron Microscope (SEM) analyses, the pinholes appear on the whole surface of the Pd/PSS membrane and this is probably due to release of sulphur from the graphite seal rings.

  18. Sensitive voltammetric sensor based on isopropanol-Nafion-PSS-GR nanocomposite modified glassy carbon electrode for determination of clenbuterol in pork.

    PubMed

    Wang, Ling; Yang, Ran; Chen, Jing; Li, Jianjun; Qu, Lingbo; de B Harrington, Peter

    2014-12-01

    In the present study, poly(sodium 4-styrenesulfonate) (PSS) functionalized graphene (GR) was synthesised via a simple one-step chemical reduction of exfoliated graphite oxides in the presence of PSS. Characterisation of as-made nanocomposite using Fourier transform infrared spectroscopy (FT-IR) and ultraviolet and visible spectroscopy (UV-vis) clearly demonstrate the successful attachment of PSS to graphene sheets. A novel clenbuterol (CLB) electrochemical sensor was fabricated based on isopropanol-Nafion-PSS-GR composite film modified glassy carbon electrode. In the Britton-Robinson buffer (pH 1.2), the sensor exhibited superior electrocatalytic activity towards the oxidation of CLB. Applying linear sweep voltammetry, a good linear relationship of the oxidation peak current with respect to concentrations of CLB cross the range of 7.5 × 10(-8)-2.5 × 10(-5)mol L(-1) and a detection limit of 2.2 × 10(-8) mol L(-1) were achieved. The proposed method was successfully applied for the determination of CLB in pork.

  19. Performance and Long-Term Stability of Pd/PSS and Pd/Al2O3 Membranes for Hydrogen Separation

    PubMed Central

    Liguori, Simona; Iulianelli, Adolfo; Dalena, Francesco; Pinacci, Pietro; Drago, Francesca; Broglia, Maria; Huang, Yan; Basile, Angelo

    2014-01-01

    The present work is focused on the investigation of the performance and long-term stability of two composite palladium membranes under different operating conditions. One membrane (Pd/porous stainless steel (PSS)) is characterized by a ~10 µm-thick palladium layer on a porous stainless steel substrate, which is pretreated by means of surface modification and oxidation; the other membrane (Pd/Al2O3) is constituted by a ~7 µm-thick palladium layer on an asymmetric microporous Al2O3 substrate. The operating temperature and pressure ranges, used for studying the performance of these two kinds of membranes, are 350–450 °C and 200–800 kPa, respectively. The H2 permeances and the H2/N2 selectivities of both membranes were investigated and compared with literature data. At 400 °C and 200 kPa as pressure difference, Pd/PSS and Pd/Al2O3 membranes exhibited an H2/N2 ideal selectivity equal to 11700 and 6200, respectively, showing stability for 600 h. Thereafter, H2/N2 selectivity of both membranes progressively decreased and after around 2000 h, dropped dramatically to 55 and 310 for the Pd/PSS and Pd/Al2O3 membranes, respectively. As evidenced by Scanning Electron Microscope (SEM) analyses, the pinholes appear on the whole surface of the Pd/PSS membrane and this is probably due to release of sulphur from the graphite seal rings. PMID:24957126

  20. Aryl sulfonates as neutral photoacid generators (PAGs) for EUV lithography

    NASA Astrophysics Data System (ADS)

    Sulc, Robert; Blackwell, James M.; Younkin, Todd R.; Putna, E. Steve; Esswein, Katherine; DiPasquale, Antonio G.; Callahan, Ryan; Tsubaki, Hideaki; Tsuchihashi, Tooru

    2009-03-01

    EUV lithography (EUVL) is a leading candidate for printing sub-32 nm hp patterns. In order for EUVL to be commercially viable at these dimensions, a continuous evolution of the photoresist material set is required to simultaneously meet the aggressive specifications for resolution, resist sensitivity, LWR, and outgassing rate. Alternative PAG designs, especially if tailored for EUVL, may aid in the formation of a material set that helps achieve these aggressive targets. We describe the preparation, characterization, and lithographic evaluation of aryl sulfonates as non-ionic or neutral photoacid generators (PAGs) for EUVL. Full lithographic characterization is reported for our first generation resist formulation using compound H, MAP-1H-2.5. It is benchmarked against MAP-1P-5.0, which contains the well-known sulfonium PAG, triphenylsulfonium triflate (compound P). Z-factor analysis indicates nZ32 = 81.4 and 16.8 respectively, indicating that our first generation aryl sulfonate formulations require about 4.8x improvement to match the results achieved with a model onium PAG. Improving the acid generation efficiency and use of the generated byproducts is key to the continued optimization of this class of PAGs. To that end, we believe EI-MS fragmentation patterns and molecular simulations can be used to understand and optimize the nature and efficiency of electron-induced PAG fragmentation.

  1. Nanostructured membranes and electrodes with sulfonic acid functionalized carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Tripathi, Bijay P.; Schieda, M.; Shahi, Vinod K.; Nunes, Suzana P.

    Herein we report the covalent functionalization of multiwall carbon nanotubes by grafting sulfanilic acid and their dispersion into sulfonated poly(ether ether ketone). The nanocomposites were explored as an option for tuning the proton and electron conductivity, swelling, water and alcohol permeability aiming at nanostructured membranes and electrodes for application in alcohol or hydrogen fuel cells and other electrochemical devices. The nanocomposites were extensively characterized, by studying their physicochemical and electrochemical properties. They were processed as self-supporting films with high mechanical stability, proton conductivity of 4.47 × 10 -2 S cm -1 at 30 °C and 16.8 × 10 -2 S cm -1 at 80 °C and 100% humidity level, electron conductivity much higher than for the plain polymer. The methanol permeability could be reduced to 1/20, keeping water permeability at reasonable values. The ratio of bound water also increases with increasing content of sulfonated filler, helping in keeping water in the polymer in conditions of low external humidity level.

  2. Rapid screening and quantification of sulfonate derivatives in white peony root by UHPLC-MS-MS.

    PubMed

    Yan, Zhixiang; Chen, Chen; Xie, Xiabing; Fu, Bo; Yang, Xinghao

    2012-02-01

    A rapid ultra-high-performance liquid chromatographic-tandem mass spectrometric (UHPLC-MS-MS) method has been developed for rapid screening and quantitative analysis of sulfonate derivatives (SDs) in commercial white peony root. Separation was performed on an Agilent Zorbax Eclipse Plus-C18 column by gradient elution with acetonitrile-0.1% (v/v) formic acid as the mobile phase. In-source fragmentation was used to generate the characteristic fragment ion at m/z 259 and to screen for nine SDs. Detection of these SDs was further performed in multiple reaction monitoring (MRM) mode to improve sensitivity and to quantify the two SDs paeoniflorin sulfonate and benzoylpaeoniflorin sulfonate. The method was validated for specificity, linearity, limits of detection and quantification, precision, accuracy, and matrix effects. Nine commercial white peony root samples were examined by use of this method, which revealed great variety in the paeoniflorin sulfonate and benzoylpaeoniflorin sulfonate content.

  3. Solid Sulfonic Acid Catalysts Based on Porous Carbons and Carbon-Silica Composites

    NASA Astrophysics Data System (ADS)

    Tian, Xiao Ning; Luo, Lijuan; Jiang, Zhongqing; Zhao, X. S.

    Mesoporous carbons prepared using a templating method under different carbonization temperatures are sulfonated with concentrated H2SO4. Without the moving of silica template carbon-silica composites were prepared, which can maintain the pore structure well during sulfonation reaction process. The resultant samples are characterized using nitrogen adsorption, transmission electron microscope, field-emission scanning electron microscope, X-ray diffraction, X-ray photoelectron spectroscopy, and elemental analysis techniques. The catalytic performances of the sulfonated carbons and composites are evaluated by esterification reaction of methanol with acetic acid. The results show that a low-temperature carbonization process is favorable for improving the reaction conversion of acetic acid. In addition, the sulfonated carbon-silica composites show a higher acetic acid conversion than the sulfonated mesoporous carbons.

  4. Synthesis and polymerization of substituted ammonium sulfonate monomers for advanced materials applications.

    PubMed

    Cavicchi, Kevin A

    2012-02-01

    Sulfonated polymers have found use as ion-exchange membranes for use in fuel cells, water purification, electroactive devices, and inorganic materials templating and synthesis. Improving the materials for these applications and opening up new applications requires the ability to synthesis targeted or more complex sulfonated polymers, which includes tailoring the chemistry (copolymerization across a wider range of solubility) and/or polymer architecture (block, graft, nanoparticle). This article will summarize the recent work using sulfonated monomers with substituted ammonium counterions as a versatile route for enabling this goal. Two main benefits of these monomers are as follows. First, they are useful for preparing amphiphilic copolymers, which is a challenge using traditional acidic or alkali salt forms of sulfonated monomers. Second, sulfonated polymers with substituted ammonium counterions are useful polymers for obtaining unique material properties, such as organo-gelation of low polarity solvents or obtaining ionic liquid polymers for the fabrication of solid polymer electrolytes.

  5. 40 CFR 417.140 - Applicability; description of the neutralization of sulfuric acid esters and sulfonic acids...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... neutralization of sulfuric acid esters and sulfonic acids subcategory. 417.140 Section 417.140 Protection of... MANUFACTURING POINT SOURCE CATEGORY Neutralization of Sulfuric Acid Esters and Sulfonic Acids Subcategory § 417.140 Applicability; description of the neutralization of sulfuric acid esters and sulfonic...

  6. 40 CFR 417.140 - Applicability; description of the neutralization of sulfuric acid esters and sulfonic acids...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... neutralization of sulfuric acid esters and sulfonic acids subcategory. 417.140 Section 417.140 Protection of... MANUFACTURING POINT SOURCE CATEGORY Neutralization of Sulfuric Acid Esters and Sulfonic Acids Subcategory § 417.140 Applicability; description of the neutralization of sulfuric acid esters and sulfonic...

  7. 40 CFR 417.140 - Applicability; description of the neutralization of sulfuric acid esters and sulfonic acids...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... neutralization of sulfuric acid esters and sulfonic acids subcategory. 417.140 Section 417.140 Protection of... MANUFACTURING POINT SOURCE CATEGORY Neutralization of Sulfuric Acid Esters and Sulfonic Acids Subcategory § 417.140 Applicability; description of the neutralization of sulfuric acid esters and sulfonic...

  8. 40 CFR 417.140 - Applicability; description of the neutralization of sulfuric acid esters and sulfonic acids...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... neutralization of sulfuric acid esters and sulfonic acids subcategory. 417.140 Section 417.140 Protection of... MANUFACTURING POINT SOURCE CATEGORY Neutralization of Sulfuric Acid Esters and Sulfonic Acids Subcategory § 417.140 Applicability; description of the neutralization of sulfuric acid esters and sulfonic...

  9. 40 CFR 417.140 - Applicability; description of the neutralization of sulfuric acid esters and sulfonic acids...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... neutralization of sulfuric acid esters and sulfonic acids subcategory. 417.140 Section 417.140 Protection of... MANUFACTURING POINT SOURCE CATEGORY Neutralization of Sulfuric Acid Esters and Sulfonic Acids Subcategory § 417.140 Applicability; description of the neutralization of sulfuric acid esters and sulfonic...

  10. Coupling hydrogen separation with butanone hydrogenation in an electrochemical hydrogen pump with sulfonated poly (phthalazinone ether sulfone ketone) membrane

    NASA Astrophysics Data System (ADS)

    Huang, Shiqi; Wang, Tao; Wu, Xuemei; Xiao, Wu; Yu, Miao; Chen, Wei; Zhang, Fengxiang; He, Gaohong

    2016-09-01

    This work reports the novel work of coupling H2/CO2 separation with biomass-derived butanone hydrogenation in non-fluorinated sulfonated poly (phthalazinone ether sulfone ketone) (SPPESK) electrochemical hydrogen pump (EHP) reactor. Due to higher resistance to swelling, SPPESK-based EHP reactor exhibits more excellent reaction rate in elevated temperature (60 °C) and higher butanone concentration (2 M) as 270, 260 nmol cm-2 s-1, respectively, higher than 240, 200 nmol cm-2 s-1of Nafion-based EHP reactors. Also, the SPPESK-based EHP reactor remains 90% of initial hydrogenation rate after 4 batches, better than that of Nafion-based EHP reactors, which is only 62%. The energy efficiency of EHP separator reaches 40% under H2/CO2 mixture feed mode, and electricity of about 0.3 kWh is consumed per Nm3 H2 product, being superior to energy consumption compared with alternative processes like PSA and electrolysis of water. In addition, SPPESK-based EHP exhibits better hydrogenation stability due to lower CO2 permeation than Nafion. With increasing CO2 content in H2 feed, hydrogenation rate almost keeps constant at around 210 nmol cm-2 s-1 in SPPESK-based EHP reactor while decreases fast to 50 nmol cm-2 s-1 in Nafion/PTFE-based EHP reactor. These results show integration of gas separation with hydrogenation reactor is feasible in SPPESK-based EHP reactor.

  11. Method of increasing enhanced oil recovery by using a novel low sulfonate phase in the polymer slug

    SciTech Connect

    Carlin, J.T.; Haferkamp, G.L.

    1987-03-10

    A process is described for enhanced hydrocarbon recovery comprising injecting into a well a surfactant fluid comprising the fraction having the highest sulfonate content which separates after settling from a mixture of water, petroleum sulfonate surfactant, solubilizer and polymer. Thereafter the remaining fraction of surfactant fluid which contains the lower sulfonate content is added to a polymer slug, injecting the polymer slug and forcing the high sulfonate content surfactant slug and subsequently the low sulfonate polymer slug through the formation and recovering the hydrocarbons.

  12. Fully aromatic block copolymers for fuel cell membranes with densely sulfonated nanophase domains.

    PubMed

    Takamuku, Shogo; Jannasch, Patric

    2011-03-01

    Two multiblock copoly(arylene ether sulfone)s with similar block lengths and ion exchange capacities (IECs) were prepared by a coupling reaction between a non-sulfonated precursor block and a highly sulfonated precursor block containing either fully disulfonated diarylsulfone or fully tetrasulfonated tetraaryldisulfone segments. The latter two precursor blocks were sulfonated via lithiation-sulfination reactions whereby the sulfonic acid groups were exclusively placed in ortho positions to the many sulfone bridges, giving these blocks IECs of 4.1 and 4.6 meq·g⁻¹, respectively. Copolymer membranes with IECs of 1.4 meq·g⁻¹ displayed well-connected hydrophilic nanophase domains and had decomposition temperatures at, or above, 300 °C under air. The copolymer with the tetrasulfonated tetraaryldisulfone segments showed a proton conductivity of 0.13 S·cm⁻¹ at 80 °C under fully humidified conditions, and surpassed that of a perfluorosulfonic acid membrane (NRE212) by a factor of 5 at -20 °C over time.

  13. Pneumocystis carinii mutations are associated with duration of sulfa or sulfone prophylaxis exposure in AIDS patients.

    PubMed

    Kazanjian, P; Armstrong, W; Hossler, P A; Burman, W; Richardson, J; Lee, C H; Crane, L; Katz, J; Meshnick, S R

    2000-08-01

    This study was conducted to determine whether Pneumocystis carinii dyhydropteroate synthase (DHPS) gene mutations in AIDS patients with P. carinii pneumonia (PCP) are affected by duration of sulfa or sulfone prophylaxis and influence response to sulfa or sulfone therapy. The P. carinii DHPS genes from 97 AIDS patients with PCP between 1991 and 1999 from 4 medical centers were amplified, using polymerase chain reaction (PCR), and sequenced. Mutations were observed in 76% of isolates from patients exposed to sulfa or sulfone prophylaxis compared with 23% of isolates from patients not exposed (P=.001). Duration of prophylaxis increased the risk of mutations (relative risk [RR] for each exposure month, 1.06; P=.02). Twenty-eight percent of patients with mutations failed sulfa or sulfone treatment; mutations increased the risk of sulfa or sulfone treatment failure (RR, 2.1; P=0.01). Thus, an increased duration of sulfa or sulfone prophylaxis increases the chance of developing a P. carinii mutation. The majority of patients with mutations respond to sulfa or sulfone therapy.

  14. Celecoxib influences steroid sulfonation catalyzed by human recombinant sulfotransferase 2A1

    PubMed Central

    Ambadapadi, Sriram; Wang, Peter L.; Palii, Sergiu P.; James, Margaret O.

    2015-01-01

    Celecoxib has been reported to switch the human SULT2A1-catalyzed sulfonation of 17βestradiol (17β-E2) from the 3- to the 17-position. The effects of celecoxib on the sulfonation of selected steroids catalyzed by human SULT2A1 were assessed through in vitro and in silico studies. Celecoxib inhibited SULT2A1-catalyzed sulfonation of dehydroepiandrosterone (DHEA), androst-5-ene-3β, 17β-diol (AD), testosterone (T) and epitestosterone (Epi-T) in a concentration-dependent manner. Low μM concentrations of celecoxib strikingly enhanced the formation of the 17-sulfates of 6-dehydroestradiol (6D-E2), 17β-dihydroequilenin (17β-Eqn), 17β-dihydroequilin (17β-Eq), and 9-dehydroestradiol (9D-E2) as well as the overall rate of sulfonation. For 6D-E2, 9D-E2 and 17β-Eqn, celecoxib inhibited 3-sulfonation, however 3-sulfonation of 17β-Eq was stimulated at celecoxib concentrations below 40 μM. Ligand docking studies in silico suggest that celecoxib binds in the substrate-binding site of SULT2A1 in a manner that prohibits the usual binding of substrates but facilitates, for appropriately shaped substrates, a binding mode that favors 17-sulfonation. PMID:25960318

  15. A model survey meter using undoped poly (ether sulfone)

    NASA Astrophysics Data System (ADS)

    Nakamura, Hidehito; Shirakawa, Yoshiyuki; Kanayama, Masaya; Sato, Nobuhiro; Kitamura, Hisashi; Takahashi, Sentaro

    2015-04-01

    The large region surrounding the damaged Fukushima Daiichi Nuclear Power Plant has necessitated the use of numerous radiation survey meters with large, robust substrates. The survey meters require efficient scintillation materials that do not require doping and have dimensional stability, such as poly (ether sulfone) (PES) resins. Here, we demonstrate the performance of a model survey meter that uses large PES plates with polished, mirrored surfaces and rough, scattering surfaces. Light collection efficiencies from plates having one or more of these surfaces were quantitatively Characterised with 36Cl-, 60Co-, 137Cs-radioactive sources. The count rates of plates having a combination of mirrored/scattering-surfaces are >1.6 times that for plates having two mirrored surfaces. In addition, a significant amount of radiation-induced light generated in the PES is trapped inside the plate because of its relatively high refractive index. The results indicate that large, undoped PES plates can be used in radiation survey meters.

  16. Synthesis and physical properties of highly sulfonated polyaniline. Technical report

    SciTech Connect

    Wei, X.L.; Bobeczko, C.; Epstein, A.J.

    1996-03-01

    Sulfonated polyaniline (EB-SPAN) is a self-doped conducting polymer. It has a high water solubility and a novel pH-dependent DC conductivity that is of interest for fundamental science and also for applications in such areas as rechargeable battery and pH control technologies. The authors report here the extensive characterization and details of synthesis of a new form of sulfonated polyaniline (LEB-SPAN) which shows novel or significantly improved chemical and physical properties. LEB-SPAN has a much high sulfur to nitrogen ratio (S/N) of N approx. 0.75, 50% larger than that previously reported for EB-SPAN, S/N approx. 0.50. This change in composition leads to significant alteration of the properties including an order of magnitude increase in the room temperature DC conductivity to approx. 1 S./cm, nearly double the solubility in water, and a completely different pH-dependence of the oxidation potential (E1/2). For LEB-SPAN the DC conductivity is unaffected by pH over the range 0 < or = pH < or = 14, strikingly different from the behavior of both parent polyaniline and EB-SPAN which become insulating for pH > or = 3 and pH > or = 7.5; respectively. Temperature-dependent DC conductivity and EPR measurements for LEB-SPAN reveal a lower activation energy for the conductivity and a higher density of states at the Fermi energy as compared with EB-SPAN. The dramatic differences in the pH-dependence of the DC conductivity, cyclic voltammetry (CV), FTIR, and UV-Vis results for LEB-SPAN and EB-SPAN are shown to be a consequence of the much higher S/N ratio in LEB-SPAN.

  17. Design, fabrication and evaluation of intelligent sulfone-selective polybenzimidazole nanofibers.

    PubMed

    Ogunlaja, Adeniyi S; du Sautoy, Carol; Torto, Nelson; Tshentu, Zenixole R

    2014-08-01

    Molecularly imprinted polybenzimidazole nanofibers fabricated for the adsorption of oxidized organosulfur compounds are presented. The imprinted polymers exhibited better selectivity for their target model sulfone-containing compounds with adsorption capacities of 28.5±0.4mg g(-1), 29.8±2.2mg g(-1) and 20.1±1.4mg g(-1) observed for benzothiophene sulfone (BTO2), dibenzothiophene sulfone (DBTO2) and 4,6-dimethyldibenzothiophene sulfone (4,6-DMDBTO2) respectively. Molecular modeling based upon the density functional theory (DFT) indicated that hydrogen bond interactions may take place between sulfone oxygen groups with NH groups of the PBI. Further DFT also confirmed the feasibility of π-π interactions between the benzimidazole rings and the aromatic sulfone compounds. The adsorption mode followed the Freundlich (multi-layered) adsorption isotherm which indicated possible sulfone-sulfone interactions. A home-made pressurized hot water extraction (PHWE) system was employed for the extraction/desorption of sulfone compounds within imprinted nanofibers at 1mL min(-1), 150°C and 30 bar. PHWE used a green solvent (water) and achieved better extraction yields compared to the Soxhlet extraction process. The application of molecularly imprinted polybenzimidazole (PBI) nanofibers displayed excellent sulfur removal, with sulfur in fuel after adsorption falling below the determined limit of detection (LOD), which is 2.4mg L(-1)S, and with a sulfur adsorption capacity of 5.3±0.4mg g(-1) observed for application in the fuel matrix.

  18. Catalytic conjugate additions of geminal bis(sulfone)s: expanding the chemistry of sulfones as simple alkyl anion equivalents.

    PubMed

    Landa, Aitor; Puente, Angel; Santos, J Ignacio; Vera, Silvia; Oiarbide, Mikel; Palomo, Claudio

    2009-11-01

    The value of cyclic gem-bis(sulfone) 4 as a simple alkyl nucleophile equivalent in catalytic C-C bond-forming reactions is demonstrated. The 1,4-type nucleophilic additions of bis(sulfone) 4 to alpha,beta-unsaturated ketones take place by assistance of catalytic guanidine base. On the other hand, pyrrolidines are able to catalyze the conjugate addition of 4 to both enones and enals, likely by means of iminium ion activation. Upon exploration of the best chiral pyrrolidine catalyst, it has been found that the addition of 4 to enals catalyzed by diphenylprolinol silyl ether 10 proceeds with very high enantioselectivity (beta-aryl-substituted enals >95% ee; beta-alkyl substituted enals up to 94% ee; ee = enantiomeric excess). Further reductive desulfonation of adducts gives rise to the corresponding beta-methyl aldehydes, as well as the derived alcohols, acetals, and methyl esters after simple (Mg, MeOH) well-established protocols. Application of the procedure to the synthesis of biologically relevant phenethyl building blocks is shown. Most interestingly, alpha-alkylation of initially obtained bis(sulfone) adducts can be done even with less reactive alkylating reagents, such as long linear-chain or branched-chain alkyl halides. Accordingly, upon the desulfonation process, a general, experimentally simple and highly enantioselective access to beta-branched aldehydes, alcohols, or esters is possible. Further exploration of the method includes the use of chiral alpha,beta-unsaturated aldehydes derived from citronellal as the Michael acceptor partners. In these instances, the sense of the conjugate addition of 4 is controlled by the chirality of the pyrrolidine catalyst, thus allowing for a stereochemically predictable access to 1,3-dimethyl arrays, such as those present in deoxygenated polyketide-type natural products. The intramolecular variation of this technology by using doubly unsaturated aldehyde-ester 22 illustrated the site selectivity of the procedure and its

  19. Magnetic graphene - polystyrene sulfonic acid nano composite: A dispersive cation exchange sorbent for the enrichment of aminoalcohols and ethanolamines from environmental aqueous samples.

    PubMed

    Chinthakindi, Sridhar; Purohit, Ajay; Singh, Varoon; Tak, Vijay; Dubey, D K; Pardasani, Deepak

    2015-12-01

    Present study aimed at graphene surface modification to achieve selective analyte binding in dispersive solid phase extraction. Magnetic graphene - polystyrene sulfonic acid (MG-PSS) cation exchange nano-composite was prepared by non-covalent wrapping method. Composite was characterized by FT-IR and zeta potential. Material exhibited good dispersion in water and high exchange capacity of 1.97±0.16mMg(-1). Prepared nano-sorbent was then exploited for the cation exchange extraction and gas chromatography mass spectrometric analysis of Chemical Weapons Convention relevant aminoalcohols and ethanolamines from aqueous samples. Extraction parameters such as sorbent amount, extraction time, desorption conditions and sample pH were optimized and effect of common matrix interferences such as polyethylene glycol and metal salts was also studied. Three milligram of sorbent per mL of sample with 20min of extraction time at room temperature afforded 70-81% recoveries of the selected analytes spiked at concentration level of 1μgmL(-1). Method showed good linearity in the studied range with r(2)≥0.993. The limits of detection and limits of quantification ranged from 23 to 54ngmL(-1) and 72 to 147ngmL(-1), respectively. The relative standard deviation for intra- and inter-day precision ranged from 4.6 to 10.2% and 7.4 to 14.8% respectively. Applicability of the method to different environmental samples as well as the proficiency tests conducted by the Organization for the Prohibition of Chemical Weapons (OPCW) was also ascertained.

  20. The influence of ionic strength and mixing ratio on the colloidal stability of PDAC/PSS polyelectrolyte complexes.

    PubMed

    Zhang, Yanpu; Yildirim, Erol; Antila, Hanne S; Valenzuela, Luis D; Sammalkorpi, Maria; Lutkenhaus, Jodie L

    2015-10-01

    Polyelectrolyte complexes (PECs) form by mixing polycation and polyanion solutions together, and have been explored for a variety of applications. One challenge for PEC processing and application is that under certain conditions the as-formed PECs aggregate and precipitate out of suspension over the course of minutes to days. This aggregation is governed by several factors such as electrostatic repulsion, van der Waals attractions, and hydrophobic interactions. In this work, we explore the boundary between colloidally stable and unstable complexes as it is influenced by polycation/polyanion mixing ratio and ionic strength. The polymers examined are poly(diallyldimethylammonium chloride) (PDAC) and poly(sodium 4-styrenesulfonate) (PSS). Physical properties such as turbidity, hydrodynamic size, and zeta potential are investigated upon complex formation. We also perform detailed molecular dynamics simulations to examine the structure and effective charge distribution of the PECs at varying mixing ratios and salt concentrations to support the experimental findings. The results suggest that the colloidally stable/unstable boundary possibly marks the screening effects from added salt, resulting in weakly charged complexes that aggregate. At higher salt concentrations, the complexes initially form and then gradually dissolve into solution.

  1. 13.2% efficiency Si nanowire/PEDOT:PSS hybrid solar cell using a transfer-imprinted Au mesh electrode

    NASA Astrophysics Data System (ADS)

    Park, Kwang-Tae; Kim, Han-Jung; Park, Min-Joon; Jeong, Jun-Ho; Lee, Jihye; Choi, Dae-Geun; Lee, Jung-Ho; Choi, Jun-Hyuk

    2015-07-01

    In recent years, inorganic/organic hybrid solar cell concept has received growing attention for alternative energy solution because of the potential for facile and low-cost fabrication and high efficiency. Here, we report highly efficient hybrid solar cells based on silicon nanowires (SiNWs) and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) using transfer-imprinted metal mesh front electrodes. Such a structure increases the optical absorption and shortens the carrier transport distance, thus, it greatly increases the charge carrier collection efficiency. Compared with hybrid cells formed using indium tin oxide (ITO) electrodes, we find an increase in power conversion efficiency from 5.95% to 13.2%, which is attributed to improvements in both the electrical and optical properties of the Au mesh electrode. Our fabrication strategy for metal mesh electrode is suitable for the large-scale fabrication of flexible transparent electrodes, paving the way towards low-cost, high-efficiency, flexible solar cells.

  2. 13.2% efficiency Si nanowire/PEDOT:PSS hybrid solar cell using a transfer-imprinted Au mesh electrode

    PubMed Central

    Park, Kwang-Tae; Kim, Han-Jung; Park, Min-Joon; Jeong, Jun-Ho; Lee, Jihye; Choi, Dae-Geun; Lee, Jung-Ho; Choi, Jun-Hyuk

    2015-01-01

    In recent years, inorganic/organic hybrid solar cell concept has received growing attention for alternative energy solution because of the potential for facile and low-cost fabrication and high efficiency. Here, we report highly efficient hybrid solar cells based on silicon nanowires (SiNWs) and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) using transfer-imprinted metal mesh front electrodes. Such a structure increases the optical absorption and shortens the carrier transport distance, thus, it greatly increases the charge carrier collection efficiency. Compared with hybrid cells formed using indium tin oxide (ITO) electrodes, we find an increase in power conversion efficiency from 5.95% to 13.2%, which is attributed to improvements in both the electrical and optical properties of the Au mesh electrode. Our fabrication strategy for metal mesh electrode is suitable for the large-scale fabrication of flexible transparent electrodes, paving the way towards low-cost, high-efficiency, flexible solar cells. PMID:26174964

  3. Improved performances of CuPc/C60-based solar cell by using randomly and irregularly embossed PEDOT:PSS as anode buffer layer

    NASA Astrophysics Data System (ADS)

    Zhang, Haiqing; Hao, Yuying; Zhang, Fan; Sun, Qinjun; Li, Zhanfeng; Cui, Yanxia; Wang, Hua; Shi, Fang

    2015-07-01

    An unique organic solar cell (OSC) based on copper phthalocyanine (CuPc) and fullerene C60 as the electron donor and acceptor materials is demonstrated with randomly and irregularly embossed poly (3, 4-ethylenedioxythiophene) poly (styrenesulfonate) (PEDOT: PSS) as anode buffer layer. The effect of PEDOT:PSS nanostructure is characterized by optical and electrical measurements. The results indicate that introducing irregular nanostructure with random distribution into OSC leads to longer light paths by efficient scattering of the incident light and thus higher light absorption in active layer. Moreover, such a nanostructure increases the junction area, allowing more efficient exciton dissociation and charge carrier transfer/collection. These combined effects result in a prominent enhancement of 25.5% in average power conversion efficiency relative to the non-structured OSC due to the increases in short-circuit current and fill factor.

  4. Enhanced Dispersion of TiO2 Nanoparticles in a TiO2/PEDOT:PSS Hybrid Nanocomposite via Plasma-Liquid Interactions

    PubMed Central

    Liu, Yazi; Sun, Dan; Askari, Sadegh; Patel, Jenish; Macias-Montero, Manuel; Mitra, Somak; Zhang, Richao; Lin, Wen-Feng; Mariotti, Davide; Maguire, Paul

    2015-01-01

    A facile method to synthesize a TiO2/PEDOT:PSS hybrid nanocomposite material in aqueous solution through direct current (DC) plasma processing at atmospheric pressure and room temperature has been demonstrated. The dispersion of the TiO2 nanoparticles is enhanced and TiO2/polymer hybrid nanoparticles with a distinct core shell structure have been obtained. Increased electrical conductivity was observed for the plasma treated TiO2/PEDOT:PSS nanocomposite. The improvement in nanocomposite properties is due to the enhanced dispersion and stability in liquid polymer of microplasma treated TiO2 nanoparticles. Both plasma induced surface charge and nanoparticle surface termination with specific plasma chemical species are proposed to provide an enhanced barrier to nanoparticle agglomeration and promote nanoparticle-polymer binding. PMID:26497265

  5. Multiscale analysis of the effect of micro-phase separation on the charge transfer at the PEDOT:PSS and P3HT:PCBM layer interface

    NASA Astrophysics Data System (ADS)

    Huang, Min

    2015-09-01

    The influence of micro phase behavior on the charge transfer at the interface between PEDOT:PSS and P3HT:PCBM layers was studied using multiscale analysis. Calculated Flory- Huggins parameters indicated that the PEDOT attracts P3HT and repulses PCBM that agrees well with the experimental observation of the development of P3HT rich interface during the BHJ layer formation. Based on the calculated Flory-Huggins parameters, mesoscale DPD simulations were conducted for PEDOT:PSS and P3HT:PCBM layers. Results were mapped to the CG (coarse grained) and then atomistic scales where atomistic details of the interface were studied. The density of nonbonding close contacts including that from reorientation between PEDOT and P3HT was quantified, vibronic coupling and carrier transfer efficiency were discussed.

  6. Enhanced Dispersion of TiO2 Nanoparticles in a TiO2/PEDOT:PSS Hybrid Nanocomposite via Plasma-Liquid Interactions

    NASA Astrophysics Data System (ADS)

    Liu, Yazi; Sun, Dan; Askari, Sadegh; Patel, Jenish; Macias-Montero, Manuel; Mitra, Somak; Zhang, Richao; Lin, Wen-Feng; Mariotti, Davide; Maguire, Paul

    2015-10-01

    A facile method to synthesize a TiO2/PEDOT:PSS hybrid nanocomposite material in aqueous solution through direct current (DC) plasma processing at atmospheric pressure and room temperature has been demonstrated. The dispersion of the TiO2 nanoparticles is enhanced and TiO2/polymer hybrid nanoparticles with a distinct core shell structure have been obtained. Increased electrical conductivity was observed for the plasma treated TiO2/PEDOT:PSS nanocomposite. The improvement in nanocomposite properties is due to the enhanced dispersion and stability in liquid polymer of microplasma treated TiO2 nanoparticles. Both plasma induced surface charge and nanoparticle surface termination with specific plasma chemical species are proposed to provide an enhanced barrier to nanoparticle agglomeration and promote nanoparticle-polymer binding.

  7. Method of increasing enhanced oil recovery by using a higher sulfonate phase obtained on polymer addition

    SciTech Connect

    Carlin, J.T.

    1987-01-13

    A process is described for enhanced hydrocarbon recovery comprising: dissolving a polymer from the group consisting of polyacrylamides and polysaccharides in a surfactant flood fluid resulting from mixing water, petroleum sulfonate-containing surfactant and solubilizer; allowing the mixture to separate; using the fraction with the highest sulfonate content as a surfactant fluid; forcing the fluid through the formation and recovering the hydrocarbons, wherein the proportion of the sulfonate-containing surfactant, solubilizer and polymer is about 0.5% to 20.0% of total solute by weight of petroleum sulfonate surfactant, about 0.1% to about 5% by weight of a solubilizer and about 0.1% to 10% by weight of polymer.

  8. Morphology and Proton Transport in Sulfonated Block Copolymer and Mesoporous Polymer Electrolyte Membranes

    NASA Astrophysics Data System (ADS)

    Chen, Chelsea; Wong, David; Beers, Keith; Balsara, Nitash

    2013-03-01

    In an effort to understand the fundamentals of proton transport in polymer electrolyte membranes (PEMs), we have developed a series of poly(styrene-b-ethylene-b-styrene) (SES) membranes. The SES membranes were subsequently sulfonated to yield proton conducting S-SES membranes. We examine the effects of sulfonation level, temperature and thermal history on the morphology of S-SES membranes in both dry and hydrated states. The effects of these parameters on water uptake and proton transport characteristics of the membranes are also examined. Furthermore, building upon the strategy we deployed in sulfonating the SES membranes, we fabricated mesoporous S-SES membranes, with pores lined up with the proton conducting channels. These membranes have three distinct phases: structural block, proton-conducting block, and void. We examine the effects of pore size, domain structure and sulfonation level on water uptake and proton conductivity of the mesoporous PEMs at different temperatures. This work is funded by Department of Energy.

  9. Titania-based molecularly imprinted polymer for sulfonic acid dyes prepared by sol-gel method.

    PubMed

    Li, Man; Li, Rong; Tan, Jin; Jiang, Zi-Tao

    2013-03-30

    A novel titania-based molecularly imprinted polymer (MIP) was synthesized through sol-gel process with sunset yellow (Sun) as template, without use of functional monomer. MIP was used as a solid-phase extraction material for the isolation and enrichment of sulfonic acid dyes in beverages. The results showed that MIP exhibited better selectivity, higher recovery and adsorption capacity for the sulfonic acid dyes compared to the non-imprinted polymer (NIP). MIP presented highest extraction selectivity to Sun when pH less than or equal to 3. The adsorption capacity was 485.9 mg g(-1), which was larger than that of NIP (384.7 mg g(-1)). The better clean-up ability demonstrated the capability of MIP for the isolation and enrichment of sulfonic acid dyes in complicated food samples. The mean recoveries for the sulfonic acid dyes on MIP were from 81.9% to 97.2% in spiked soft drink.

  10. EFFECTS OF PRENATAL PERFLUOROOCTANE SULFONATE (PFOS) EXPOSURE ON LUNG MATURATION IN THE PERINATAL RAT

    EPA Science Inventory

    Background: Perfluorooctane sulfonate (PFOS), found widely in wildlife and humans, is environmentally and metabolically stable. Environmental PFOS may be from its use as a surfactant, hydrolysis of perfluorooctanesulfonyl fluoride, and degradation of N-alkyl-perfluorooctanesulfon...

  11. Preparation of a sulfonated carbonaceous material from lignosulfonate and its usefulness as an esterification catalyst.

    PubMed

    Lee, Duckhee

    2013-07-10

    Sulfonated carbonaceous material useful as a solid acid catalyst was prepared from lignosulfonate, a waste of the paper-making industry sulfite pulping process, and characterized by 13C-NMR, FT-IR, TGA, SEM and elemental analysis, etc. The sulfonic acid group density and total density of all acid groups in the sulfonated carbonaceous material was determined by titration to be 1.24 mmol/g and 5.90 mmol/g, respectively. Its catalytic activity in the esterification of cyclohexanecarboxylic acid with anhydrous ethanol was shown to be comparable to that of the ionic exchange resin Amberlyst-15, when they were used in the same amount. In the meantime, the sulfonic acid group was found to be leached out by 26%-29% after it was exposed to hot water (95 °C) for 5 h. The catalytic usefulness of the prepared carbonaceous material was investigated by performing esterifications.

  12. Effective catalytic conversion of cellulose into high yields of methyl glucosides over sulfonated carbon based catalyst.

    PubMed

    Dora, Sambha; Bhaskar, Thallada; Singh, Rawel; Naik, Desavath Viswanatha; Adhikari, Dilip Kumar

    2012-09-01

    An amorphous carbon based catalyst was prepared by sulfonation of the bio-char obtained from fast pyrolysis (N(2) atm; ≈ 550°C) of biomass. The sulfonated carbon catalyst contained high acidity of 6.28 mmol/g as determined by temperature programmed desorption of ammonia of sulfonated carbon catalyst and exhibited high catalytic performance for the hydrolysis of cellulose. Amorphous carbon based catalyst containing -SO(3)H groups was successfully tested and the complete conversion of cellulose in methanol at moderate temperatures with high yields ca. ≥ 90% of α, β-methyl glucosides in short reaction times was achieved. The methyl glucosides formed in methanol are more stable for further conversion than the products formed in water. The carbon catalyst was demonstrated to be stable for five cycles with slight loss in catalytic activity. The utilization of bio-char as a sulfonated carbon catalyst provides a green and efficient process for cellulose conversion. PMID:22776237

  13. Magnetite-supported sulfonic acid: a retrievable nanocatalyst for the Ritter reaction and multicomponent reactions

    EPA Science Inventory

    Magnetite-sulfonic acid (NanocatFe-OSO3H), prepared by wet-impregnation method, serves as a magnetically retrievable sustainable catalyst for the Ritter reaction which can be used in several reaction cycles without any loss of activity.

  14. Synthesis and characterizations of electrospun sulfonated poly (ether ether ketone) SPEEK nanofiber membrane

    NASA Astrophysics Data System (ADS)

    Hasbullah, N.; Sekak, K. A.; Ibrahim, I.

    2016-07-01

    A novel electrospun polymer electrolyte membrane (PEM) based on Sulfonated Poly (ether ether ketone) were prepared and characterized. The poly (ether ether ketone) PEEK was sulfonated using concentrated sulfuric acid at room temperature for 60 hours reaction time. The degree sulfonation (DS) of the SPEEK are 58% was determined by H1 NMR using area under the peak of the hydrogen shielding at aromatic ring of the SPEEK. Then, the functional group of the SPEEK was determined using Fourier transfer infrared (FTIR) showed O-H vibration at 3433 cm-1 of the sulfonated group (SO2-OH). The effect of the solvent and polymer concentration toward the electrospinning process was investigated which, the DMAc has electrospun ability compared to the DMSO. While, at 20 wt.% of the polymer concentration able to form a fine and uniform nanofiber, this was confirmed by FESEM that shown electrospun fiber mat SPEEK surface at nano scale diameter.

  15. Effect of sulfonation and diethanolamine addition on the mechanical and physicochemical properties of SEPS copolymer

    NASA Astrophysics Data System (ADS)

    Patiño, D.; Correa, E.; Acevedo-Morantes, M.

    2016-02-01

    Modification techniques have been developed to achieve changes in the processing of polymers, and modification of their mechanical, thermal and morphological properties, as well as their hydrophobicity and conductivity. Sulfonation improves ion conductivity, antistatic behaviour, hydrophilicity and solubility of the polymers. These characteristics are related to the presence of sulfonic groups in the polymer matrix. This research project focuses on the evaluation of mechanical, physical and chemical properties of membranes that are based on a sulfonated Styrene-Ethylene-Propylene-Styrene (SEPS) copolymer. The membranes were functionalized with diethanolamine at 5, 15 and 30% w/w, to separate carbon dioxide. FTIR and XRD analyses were used to characterize the membranes. The sulfonated-loaded membrane with 15% of diethanolamine showed the best results in each characterization.

  16. Anhydrous state proton and lithium ion conducting solid polymer electrolytes based on sulfonated bisphenol-A-poly(arylene ethers)

    NASA Astrophysics Data System (ADS)

    Guha Thakurta, Soma

    Sulfonated polymer based solid polymer electrolytes (SPEs) have received considerable interest in recent years because of their wide variety of applications particularly in fuel cells, batteries, supercapacitors, and electrochromic devices. The present research was focused on three interrelated subtopics. First, two different bisphenol-A-poly(arylene ethers), polyetherimide (PEI) and polysulfone (PSU) were sulfonated by a post sulfonation method to various degrees of sulfonation, and their thermal and mechanical properties were examined. The effects of poly(arylene ether) chemical structure, reaction time, concentration, and types of sulfonating agents on sulfonation reaction were investigated. It was found that deactivation of bisphenol A unit caused by the electron withdrawing imide, retarded the sulfonation of PEI compared to PSU. Sulfonation conducted with a high concentration of sulfonating agent and/or prolonged reaction time exhibited evidence of degradation at the isopropylidene unit. The degradation occurred through the same mechanistic pathway with the two different sulfonating agents, chlorosulfonic acid (CSA) and trimethylsilyl chlorosulfonate (TMSCS). The degradation was faster with CSA than its silyl ester, TMSCS, and was evident even at low acid concentration. Second, novel anhydrous proton conducting solid polymer electrolytes (SPEs) were prepared by the incorporation of 1H-1,2,4-triazole (Taz) as a proton solvent in sulfonated polyetherimide (SPEI) matrix. The size, shape, and state of dispersion (crystal morphology) of triazole crystals in SPEI were examined as a function of degree of sulfonation and triazole concentration. Increasing sulfonic acid content caused reduction of triazole crystallite size, hence the depression of melting temperature and their uniform distribution throughout the sulfonated polymer matrix. The increased rate of structure diffusion within the smaller size crystals due to the improved molecular mobility contributed

  17. Synthesis, structure, theoretical calculations and biological activity of sulfonate active ester new derivatives

    NASA Astrophysics Data System (ADS)

    Ghazzali, Mohamed; Khattab, Sherine A. N.; Elnakady, Yasser A.; Al-Mekhlafi, Fahd A.; Al-Farhan, Khalid; El-Faham, Ayman

    2013-08-01

    A series of naphthyl and tolyl sulfonate ester were synthesized and characterized by H NMR. X-ray single crystal diffraction experiments established the molecular structure of three new sulfonate esters derivatives, and spectral data agree with these in solution. The observed hydrogen bonding is discussed on the basis of crystal structural analyses and DFT/MP2 geometry optimization quantum calculations. Antimicrobial activities were screened for selected compounds against three human cancer cell lines and Mosquito Culex pipiens larvae.

  18. Asymmetrical Self-assembly From Fluorinated and Sulfonated Block Copolymers in Aqueous Media

    SciTech Connect

    Wang, Xiaojun; Hong, Kunlun; Baskaran, Durairaj; Goswami, Monojoy; Sumpter, Bobby G; Mays, Jimmy

    2011-01-01

    Block copolymers of fluorinated isoprene and partially sulfonated styrene form novel tapered rods and ribbon-like micelles in aqueous media due to a distribution of sulfonation sites and a large Flory-Huggins interaction parameter. A combination of microscopy, light scattering, and simulation demonstrates the presence of these unique nanostructures. This study sheds light on the micellization behavior of amphiphilic block polymers by revealing a new mechanism of self-assembly.

  19. Sulfonate-cosurfactant mixtures for use in hard brines during oil recovery operations

    SciTech Connect

    Meister, J. J.

    1981-05-12

    Alkyl vinyl ether-maleic anhydride copolymers, alone or in combination with ethoxylated acids and/or ethoxylated amides and, optionally, together with polyalkoxylated carboxylic acids, polyalkoxylated amides and sulfated derivatives thereof, ethoxylated alkyl phenols, ethoxylated alcohols and the corresponding sulfated derivatives, sulfated aliphatic alcohols and alkylene oxide block copolymers, are useful to stabilize sulfonate surfactants, E.G., petroleum sulfonates, E.G., for use in tertiary oil recovery.

  20. Characterization of three deoxynivalenol sulfonates formed by reaction of deoxynivalenol with sulfur reagents.

    PubMed

    Schwartz, Heidi Elisabeth; Hametner, Christian; Slavik, Veronika; Greitbauer, Oliver; Bichl, Gerlinde; Kunz-Vekiru, Elisavet; Schatzmayr, Dian; Berthiller, Franz

    2013-09-18

    Reduction of the Fusarium mycotoxin deoxynivalenol (DON) in animal feed by treatment with sodium bisulfite and sodium metabisulfite has been successfully demonstrated in several studies. All of them reported formation of one DON sulfonate of strongly reduced toxicity compared to DON. The starting point of the present work was investigation of different sulfur reagents for reduction of DON. In the course of these experiments, three different DON sulfonates termed DON sulfonate 1 (1), DON sulfonate 2 (2), and DON sulfonate 3 (3) were identified and structurally elucidated by UHPLC-HRMS/MS as well as NMR spectroscopy. Compound 1 is characterized by loss of the epoxide group, and 2 by formation of a hemiketal. Compound 3 is an equilibrating mixture of two isomers, a ketone and a hemiketal. The MS/MS pattern can be used to differentiate the three DON sulfonates, despite their same mass and molecular formula. Investigation of parameters influencing formation and stability of DON sulfonates revealed that rapid formation of 1 and 2 occurs at alkaline pH, whereas at acidic pH, slow formation of 3 takes place, irrespective of the sulfur reagent used. Whereas 1 and 2 are stable across a broad pH range, 3 decomposes to DON, 1, and 2 at alkaline pH. In addition, both 2 and 3 are unstable in solid form. The formation, characterization, and stability of three novel DON sulfonates with respect to results from previous studies are discussed, providing insights of relevance for detoxification of DON-containing animal feed.

  1. Activated-sludge nitrification in the presence of linear and branched-chain alkyl benzene sulfonates.

    PubMed

    Baillod, C R; Boyle, W C

    1968-01-01

    The effects of biodegradable linear alkyl benzene sulfonate and branched-chain alkyl benzene sulfonate detergents on activated-sludge nitrification were investigated by administering a synthetic waste containing up to 23 mg of each detergent per liter to eight bench-scale, batch, activated-sludge units. It was found that both detergents tended to promote complete oxidation of ammonia to nitrate, whereas control units produced approximately equal amounts of nitrite and nitrate. Various hypotheses are offered to explain the phenomenon.

  2. Viscoelastic Behavior of Low Molecular Weight Sulfonated Polystyrene Ionomers

    NASA Astrophysics Data System (ADS)

    Zhao, Hongying

    Ionomers are those hydrophobic polymers having small amounts of bonded ionic groups. The introduction of the ionic groups into polymer chain produces large changes in the physical, mechanical and rheological properties of the parent polymer. Characterization of the effect of the ionic interactions on the rheology is complicated by the difficulty in separating effects due to molecular entanglements and the ionic interactions. In this study, low molecular weight (Mw=4000) sulfonated polystyrene (SPS) was used to study the dynamic and steady shear rheology of SPS ionomers. The polymer chain length used was far below the entanglement molecular weight of polystyrene and effects of molecular entanglements will be absent. Any polymer chain entanglements or lengthening behavior on the melt rheology should be due to the ionic interactions. Random SPS ionomers with two sulfonation levels were examined, 2.5 and 4.8 mol%, which corresponded, respectively, to one and two sulfonate groups per chain on average. The metal counterions was varied across the alkali metal series of the periodic table. Morphology of the ionomer was characterized by using small angle x-ray scattering (SAXS) analysis, and dynamic and steady shear measurements were performed to investigate rheological behavior of the ionomers. Glass transition temperatures of the ionomers increased with increasing ion concentration but were insensitive to cation used. The scattering peak in SAXS indicates the existence of the nanophase separated ionic clusters. The strong ionic nanophase persist up to very high temperatures and is not sensitive to the external stress. Time-temperature superposition (TTS) of G' worked reasonably well while TTS of G" failed for most ionomers. Ionic interactions increased the terminal relaxation time of the melts as much as seven orders of magnitude greater than the unentangled PS melt. The zero shear viscosity and first normal stress coefficients scaled with cq/a, where c was the

  3. Composite proton exchange membrane based on sulfonated organic nanoparticles

    NASA Astrophysics Data System (ADS)

    Pitia, Emmanuel Sokiri

    As the world sets its sight into the future, energy remains a great challenge. Proton exchange membrane (PEM) fuel cell is part of the solution to the energy challenge because of its high efficiency and diverse application. The purpose of the PEM is to provide a path for proton transport and to prevent direct mixing of hydrogen and oxygen at the anode and the cathode, respectively. Hence, PEMs must have good proton conductivity, excellent chemical stability, and mechanical durability. The current state-of-the-art PEM is a perfluorosulfonate ionomer, Nafion®. Although Nafion® has many desirable properties, it has high methanol crossover and it is expensive. The objective of this research was to develop a cost effective two-phase, composite PEM wherein a dispersed conductive organic phase preferentially aligned in the transport direction controls proton transport, and a continuous hydrophobic phase provides mechanical durability to the PEM. The hypothesis that was driving this research was that one might expect better dispersion, higher surface to volume ratio and improved proton conductivity of a composite membrane if the dispersed particles were nanometer in size and had high ion exchange capacity (IEC, = [mmol sulfonic acid]/gram of polymer). In view of this, considerable efforts were employed in the synthesis of high IEC organic nanoparticles and fabrication of a composite membrane with controlled microstructure. High IEC, ~ 4.5 meq/g (in acid form, theoretical limit is 5.4 meq/g) nanoparticles were achieved by emulsion copolymerization of a quaternary alkyl ammonium (QAA) neutralized-sulfonated styrene (QAA-SS), styrene, and divinylbenzene (DVB). The effects of varying the counterion of the sulfonated styrene (SS) monomer (alkali metal and QAA cations), SS concentration, and the addition of a crosslinking agent (DVB) on the ability to stabilize the nanoparticles to higher IECs were assessed. The nanoparticles were ion exchanged to acid form. The extent of ion

  4. Rear-Sided Passivation by SiNx:H Dielectric Layer for Improved Si/PEDOT:PSS Hybrid Heterojunction Solar Cells

    NASA Astrophysics Data System (ADS)

    Sun, Yiling; Gao, Pingqi; He, Jian; Zhou, Suqiong; Ying, Zhiqin; Yang, Xi; Xiang, Yong; Ye, Jichun

    2016-06-01

    Silicon/organic hybrid solar cells have recently attracted great attention because they combine the advantages of silicon (Si) and the organic cells. In this study, we added a patterned passivation layer of silicon nitride (SiNx:H) onto the rear surface of the Si substrate in a Si/poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) hybrid solar cell, enabling an improvement of 0.6 % in the power conversion efficiency (PCE). The addition of the SiNx:H layer boosted the open circuit voltage ( V oc) from 0.523 to 0.557 V, suggesting the well-passivation property of the patterned SiNx:H thin layer that was created by plasma-enhanced chemical vapor deposition and lithography processes. The passivation properties that stemmed from front PEDOT:PSS, rear-SiNx:H, front PEDOT:PSS/rear-SiNx:H, etc. are thoroughly investigated, in consideration of the process-related variations.

  5. Aligned/unaligned conducting polymer cryogels with three-dimensional macroporous architectures from ice-segregation-induced self-assembly of PEDOT-PSS.

    PubMed

    Zhang, Xuetong; Li, Chunyan; Luo, Yunjun

    2011-03-01

    Porous conducting polymers are of great interest because of the huge potential to combine high surface areas in the dry state with physical properties relevant to organic electronics. Aligned or unaligned conducting polymer cryogels with 3D macroporous architectures have been prepared using the ice-segregation-induced self-assembly (ISISA) of different poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT-PSS) freezing precursors as a dispersion or a formed hydrogel. The chemical composition and molecular structure of the resulting conducting polymer cryogels have been investigated by X-ray photoelectron spectroscopy and Raman spectroscopy, respectively. The morphologies of the PEDOT-PSS cryogels, together with their textural structures, have been revealed by scanning electron microscopy, mercury porosimetry, and nitrogen sorption tests. Processing PEDOT-PSS via ISISA endows the conducting polymers with novel properties, as demonstrated by a series of X-ray diffraction, differential scanning calorimetry, and electrical conductivity tests. These conducting polymer cryogels with aligned/unaligned macroporous architectures suggest the potential in the development of electronic components, tissue engineering, and next-generation catalytic and separation supports. PMID:21247212

  6. Polymer electrolytes based on sulfonated polysulfone for direct methanol fuel cells

    NASA Astrophysics Data System (ADS)

    Lufrano, F.; Baglio, V.; Staiti, P.; Arico', A. S.; Antonucci, V.

    This paper reports the development and characterization of sulfonated polysulfone (SPSf) polymer electrolytes for direct methanol fuel cells. The synthesis of sulfonated polysulfone was performed by a post sulfonation method using trimethyl silyl chlorosulfonate as a mild sulfonating agent. Bare polysulfone membranes were prepared with two different sulfonation levels (60%, SPSf-60 and 70%, SPSf-70), whereas, a composite membrane of SPSf-60 was prepared with 5 wt% silica filler. These membranes were investigated in direct methanol fuel cells (DMFCs) operating at low (30-40 °C) and high temperatures (100-120 °C). DMFC power densities were about 140 mW cm -2 at 100 °C with the bare SPSf-60 membrane and 180 mW cm -2 at 120 °C with the SPSf-60-SiO2 composite membrane. The best performance achieved at ambient temperature using a membrane with high degree of sulfonation (70%, SPSf-70) was 20 mW cm -2 at atmospheric pressure. This makes the polysulfone-based DMFC suitable for application in portable devices.

  7. Quantitative determination of fluorotelomer sulfonates in groundwater by LC MS/MS.

    PubMed

    Schultz, Melissa M; Barofsky, Douglas F; Field, Jennifer A

    2004-03-15

    Aqueous film-forming foams (AFFF) are complex mixtures containing fluorocarbon- and hydrocarbon-based surfactants that are used to fight hydrocarbon-fueled fires. The military is the largest consumer of AFFF in the United States, and fire-training activities conducted at military bases have led to groundwater contamination by unspent fuels and AFFF chemicals. A direct-injection, liquid-chromatography tandem mass spectrometry (LC MS/MS) method was developed to quantify a suite of fluorotelomer sulfonate surfactants in groundwater collected from military bases where fire-training activities were conducted. The 4:2, 6:2, and 8:2 fluorotelomer sulfonates were detected and quantified in groundwater from two of the three military bases. The total fluorotelomer sulfonate concentrations observed at Wurtsmith AFB, MI, and Tyndall AFB, FL, ranged respectively from below quantitation (< or = 0.60) to 182 microg/L and from 1100 to 14,600 microg/L. Analyses of a fluorotelomer-based AFFF concentrate by negative ion fast atom bombardment/mass spectrometry and LC MS/MS analyses indicate that the AFFF concentrate contains only a small amount of fluorotelomer sulfonates and that fluoroalkylthioamido sulfonates are the main anionic fluorosurfactant in the mixtures. More research is needed to determine the fate of fluoroalkylthioamido sulfonates in the environment.

  8. Sulfonation and anticoagulant activity of fungal exocellular β-(1→6)-D-glucan (lasiodiplodan).

    PubMed

    Vasconcelos, Ana Flora D; Dekker, Robert F H; Barbosa, Aneli M; Carbonero, Elaine R; Silveira, Joana L M; Glauser, Bianca; Pereira, Mariana Sá; Corradi da Silva, Maria de Lourdes

    2013-02-15

    An exocellular β-(1→6)-D-glucan (lasiodiplodan) produced by a strain of Lasiodiplodia theobromae (MMLR) grown on sucrose was derivatized by sulfonation to promote anticoagulant activity. The structural features of the sulfonated β-(1→6)-D-glucan were investigated by UV-vis, FT-IR and (13)C NMR spectroscopy, and the anticoagulant activity was investigated by the classical coagulation assays APTT, PT and TT using heparin as standard. The content of sulfur and degree of substitution of the sulfonated glucan was 11.73% and 0.95, respectively. UV spectroscopy showed a band at 261 nm due to the unsaturated bond formed in the sulfonation reaction. Results of FT-IR and (13)C NMR indicated that sulfonyl groups were inserted on the polysaccharide. The sulfonated β-(1→6)-D-glucan presented anticoagulant activity as demonstrated by the increase in dose dependence of APTT and TT, and these actions most likely occurred because of the inserted sulfonate groups on the polysaccharide. The lasiodiplodan did not inhibit the coagulation tests. PMID:23399236

  9. Synthesis and properties of radiopaque polymer hydrogels II: copolymers of 2,4,6-triiodophenyl- or N-(3-carboxy-2,4,6-triiodophenyl)- acrylamide and p-styrene sulfonate

    NASA Astrophysics Data System (ADS)

    Okamura, Masahiko; Yamanobe, Takeshi; Arai, Tomohiro; Uehara, Hiroki; Komoto, Tadashi; Hosoi, Seiichi; Kumazaki, Tatsuo

    2002-01-01

    In order to pursue a possibility of application of radiopaque polymer hydrogels to vascular embolization, studies were made on synthesis of iodine containing copolyanions and properties of their hydrogels with polycation via formation of polyion complexes (PIC). Acrylamide derivatives having triiodophenyl groups were synthesized and copolymerized with sodium styrene sulfonate (SS) under several conditions. It was found that N-(3-carboxy-2,4,6-triiodophenyl)-acrylamide (CIPA) and 2,4,6-triiodophenylacrylamide (TIPA) monomers are effectively copolymerized with SS, while N-allyl-2,3,5-triiodobenzamide (ATIBA) are hardly copolymerized. Hydrogels were prepared by mixing aqueous solutions of polyanions, i.e. the copolymers (PCIPA and PTIPA) and polyallylamine (PAAn). 13C NMR spectra of PCIPA/PAAn and PTIPA/PAAn hydrogels gave peaks for both polyanion and polycation. This means that there remained free anionic and cationic monomer units, which did not form ion pairs because of spatial hindrance. Time dependence of 1H T2 showed quick increment and plateau for PSS/PAAn and gradual increments for PCIPA/PAAn. Therefore, PIC containing the radiopaque copolymer retains the hydrogel state for a long time. Embolization was examined by injection of PCIPA/PAAn hydrogels into the vein of a removed porcine kidney as a preliminary test for transcatheter arterial embolization (TAE). X-ray radiograms of the embolized organ were reasonably explained based on the structure and mobility of hydrogels.

  10. Rituximab Effectiveness and Safety for Treating Primary Sjögren’s Syndrome (pSS): Systematic Review and Meta-Analysis

    PubMed Central

    Souza, Francine Bertolais do Valle; Porfírio, Gustavo José Martiniano; Andriolo, Brenda Nazaré Gomes; de Albuquerque, Julia Vajda; Trevisani, Virginia Fernandes Moça

    2016-01-01

    Background Primary Sjögren’s Syndrome (pSS) is a systemic autoimmune disease that involves the exocrine glands and internal organs. pSS leads to destruction and loss of secretory function due to intense lymphoplasmacytic infiltration. Therapeutic options include mainly symptomatic and supportive measures, and traditional immunosuppressant drugs have shown no effectiveness in randomized trials. Rituximab (RTX) is a chimeric antibody anti-CD20 that leads to B cell depletion by diverse mechanisms. There is evidence that this drug may be effective for treating pSS. The objective of this systematic review was to evaluate Rituximab effectiveness and safety for treating pSS. Methods and Findings We conducted a systematic review of RCTs published until December 2015, with no language restriction. We registered a protocol on Plataforma Brasil (40654814.6.0000.5505) and developed search strategies for the following scientific databases: MEDLINE, EMBASE, CENTRAL and LILACS. We included adults with established pSS diagnosis and considered the use of Rituximab as intervention and the use of other drugs or placebo as control. Four studies met our eligibility criteria: three with low risk of bias and one with uncertain risk of bias. The total number of participants was 276 (145 RTX, 131 placebo). We assessed the risk of bias of each included study and evaluated the following as primary outcomes: lacrimal gland function, salivary gland function, fatigue improvement and adverse events. We found no significant differences between the groups in the Schirmer test at week 24 meta-analysis (MD 3.59, 95% CI -2.89 to 10.07). Only one study evaluated the lissamine green test and reported a statistically significant difference between the groups at week 24 (MD -2.00, 95% CI -3.52 to -0.48). There was a significant difference between the groups regarding salivary flow rate (MD 0.09, 95% CI 0.02 to 0.16) and improvement in fatigue VAS at weeks 6 (RR 3.98, 95% CI 1.61 to 9.82) and week 16

  11. Perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) contamination from textiles.

    PubMed

    Supreeyasunthorn, Phenpimuk; Boontanon, Suwanna K; Boontanon, Narin

    2016-01-01

    The goals of this study were to determine the concentrations of perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) in textiles and to determine PFOS and PFOA contamination in textile washing water. Quantification analysis was performed by high performance liquid chromatography coupled with tandem mass spectrometry. Analysis of 32 textile samples by methanol extraction revealed that the average concentrations of PFOS and PFOA were 0.18 µg m(-2) (0.02 to 0.61 µg m(-2)) and 2.74 µg m(-2) (0.31 to 14.14 µg m(-2)), respectively. Although the average concentration of PFOS found in textile samples was below European Union (EU) Commission regulations (<1 µg m(-2)), the average concentration of PFOA was 2.74 µg m(-2), and 68.75% of textile samples had PFOA concentrations exceeding 1 µg m(-2). Thus, based on these results, the concentration of PFOA in products should also be regulated. Experiments on PFOS and PFOA leaching into washing water were conducted. The maximum concentrations of PFOS and PFOA were measured after the first washing; the concentrations gradually decreased with each subsequent washing. PFOS and PFOA migrated from textiles and were released into the environment, with disappearance percentages of 29.8% for PFOS and 99% for PFOA. The data presented in this study showed that textiles could be a significant direct and indirect source of PFOS and PFOA exposure for both humans and the environment.

  12. Photodynamic therapy for experimental intraocular melanoma using chloroaluminum sulfonated phthalocyanine

    SciTech Connect

    Panagopoulos, J.A.; Svitra, P.P.; Puliafito, C.A.; Gragoudas, E.S.

    1989-06-01

    Chloroaluminum sulfonated phthalocyanine (CASPc), a novel photosensitizing dye, was evaluated for treatment of experimental intraocular melanoma in 33 rabbit eyes. An argon ion pumped dye laser, operating at an emission of 675 nm, was used in a nonthermal mode to irradiate iris tumors in rabbits 24 hours after they received in intravenous dye injection (23 eyes). The effects of laser irradiation alone and dye alone were examined in ten control eyes. A threshold tumoricidal dose was established for photodynamic therapy with CASPc and laser irradiation. Vascular occlusion was produced in a well-circumscribed area corresponding to the boundaries of laser irradiation after CASPc injection. Tumors successfully treated with CASPc and laser irradiation were arrested in growth and exhibited no viable tumor cells on histologic examination. Control tumors continued rapid growth, unaffected by dye or laser. Our data indicate that CASPc demonstrates a strong photosensitizing effect on both tumor and normal tissue. These results suggest that CASPc is a potential photosensitizing compound that may be useful in the treatment of choroidal melanoma.

  13. Phthalocyanines And Their Sulfonated Derivatives As Photosensitizers In Photodynamic Therapy.

    NASA Astrophysics Data System (ADS)

    Riesz, Peter; Krishna, C. Murali

    1988-02-01

    Photodynamic therapy (PDT) of human tumors with hematoporphyrin derivative (HpD) has achieved encouraging results. However, HpD is a complex mixture whose composition varies in different preparations and with time of storage. The future promise of PDT for cancer treatment depends on the development of new chemically defined sensitizers which absorb more strongly than HpD in the 600-800 nm region. A shift to higher wavelengths is desirable since it allows increased light penetration in human tissues. In vivo, these sensitizers should be non-toxic, localize selectively in tumors and generate cytotoxic species upon illumination with a high quantum yield. These damaging species may be singlet oxygen (1O2) produced by the transfer of energy from the triplet state of the sensitizer to oxygen (Type II) or superoxide anion radicals formed by electron transfer to oxygen or substrate radicals generated by electron or hydrogen transfer directly from the sensitizer (Type I). The recent work of several groups indicating that phthalocyanines and their water soluble derivatives are promising candidates for PDT is reviewed. The photophysics, photochemistry, photosensitized killing of cultured mammalian cells and the use for in vivo photodynamic therapy of phthalocyanines is outlined. Our studies of the post-illumination photohemolysis of human red blood cells as a model system for membrane photomodification sensitized by phthalocyanine sulfonates are consistent with the predominant role of 1O2 as the damaging species.

  14. Determination of perfluoroalkyl carboxylic, sulfonic, and phosphonic acids in food.

    PubMed

    Ullah, Shahid; Alsberg, Tomas; Vestergren, Robin; Berger, Urs

    2012-11-01

    A sensitive and accurate method was developed and validated for simultaneous analysis of perfluoroalkyl carboxylic acids, sulfonic acids, and phosphonic acids (PFPAs) at low picograms per gram concentrations in a variety of food matrices. The method employed extraction with acetonitrile/water and cleanup on a mixed-mode co-polymeric sorbent (C8 + quaternary amine) using solid-phase extraction. High-performance liquid chromatographic separation was achieved on a C18 column using a mobile phase gradient containing 5 mM 1-methyl piperidine for optimal chromatographic resolution of PFPAs. A quadrupole time-of-flight high-resolution mass spectrometer operating in negative ion mode was used as detector. Method detection limits were in the range of 0.002 to 0.02 ng g(-1) for all analytes. Sample preparation (extraction and cleanup) recoveries at a spiking level of 0.1 ng g(-1) to a baby food composite were in the range of 59 to 98 %. A strong matrix effect was observed in the analysis of PFPAs in food extracts, which was tentatively assigned to sorption of PFPAs to the injection vial in the solvent-based calibration standard. The method was successfully applied to a range of different food matrices including duplicate diet samples, vegetables, meat, and fish samples.

  15. Fate of linear alkylbenzene sulfonate in the Mississippi River

    USGS Publications Warehouse

    Tabor, C.F.; Barber, L.B.

    1996-01-01

    The 2 800-km reach of the Mississippi River between Minneapolis, MN, and New Orleans, LA, was examined for the occurrence and fate of linear alkylbenzene sulfonate (LAS), a common anionic surfactant found in municipal sewage effluents. River water and bottom sediment were sampled in the summer and fall of 1991 and in the spring of 1992. LAS was analyzed using solid- phase extraction/derivatization/gas chromatography/mass spectrometry. LAS was present on all bottom sediments at concentrations ranging from 0.01 to 20 mg/kg and was identified in 21% of the water samples at concentrations ranging from 0.1 to 28.2 ??g/L. The results indicate that LAS is a ubiquitous contaminant on Mississippi River bottom sediments and that dissolved LAS is present mainly downstream from the sewage outfalls of major cities. The removal of the higher LAS homologs and external isomers indicates that sorption and biodegradation are the principal processes affecting dissolved LAS. Sorbed LAS appears to degrade slowly.

  16. Amitriptyline, clomipramine, and doxepin adsorption onto sodium polystyrene sulfonate

    PubMed Central

    2014-01-01

    Purpose of the study Comparative in vitro studies were carried out to determine the adsorption characteristics of 3 drugs on activated charcoal (AC) and sodium polystyrene sulfonate (SPS). Activated charcoal (AC) has been long used as gastric decontamination agent for tricyclic antidepressants (TCA). Methods Solutions containing drugs (amitriptyline, clomipramine, or doxepin) and variable amount of AC or SPS were incubated for 30 minutes. Results At pH 1.2 the adsorbent: drug mass ratio varied from 2 : 1 to 40 : 1 for AC, and from 0.4 : 1 to 8 : 1 for SPS. UV–VIS spectrophotometer was used for the determination of free drug concentrations. The qmax of amitriptyline was 0.055 mg/mg AC and 0.574 mg/mg SPS, qmax of clomipramine was 0.053 mg/mg AC and 0.572 mg/mg SPS, and qmax of doxepin was 0.045 mg/mg AC and 0.556 mg/mg SPS. The results of adsorption experiments with SPS revealed higher values for the qmax parameters in comparison with AC. Conclusion In vitro gastric decontamination experiments for antidepressant amitriptyline, clomipramine, and doxepin showed that SPS has higher qmax values than the corresponding experiments with AC. Therefore, we suggest SPS is a better gastric decontaminating agent for the management of acute TCA intoxication. PMID:24450391

  17. Partitioning characteristics of perfluorooctane sulfonate between water and foods.

    PubMed

    Xiao, Feng; Simcik, Matt F; Gulliver, John S

    2012-01-01

    As a persistent, bioaccumulative, and toxic organic pollutant, perfluorooctane sulfonate (PFOS) has been found ubiquitously in the environment, including in tap water. For the first time, we studied PFOS sorption from water to foods (nine commonly consumed vegetables, three meats, and cereals) at two temperatures to estimate the daily intake of PFOS attributable to cooking and food preparation. The values of the food water-distribution coefficient (KF/W, l/kg) of PFOS ranged from 7 to 19 l/kg for most vegetables and from 19 to 38 l/kg for meats. Celery exhibited the highest affinity toward PFOS (KF/W=39.8±3.4 l/kg), whereas onions showed the lowest affinity toward PFOS (KF/W=1.1±0.4 l/kg). Adding table salt (sodium chloride) greatly increased PFOS sorption in most foods, except for celery and meats. The results indicate that human exposure to PFOS could result from the sorption of PFOS from water to food during food preparation, especially when using table salt. The average daily intake of PFOS through this route was estimated. Furthermore, raw and unprocessed foods (vegetables, meats, and cereals) bought from farmers' markets and grocery stores were basically free of PFOS and other long-chain perfluoroalkyl acids.

  18. Partitioning characteristics of perfluorooctane sulfonate between water and foods.

    PubMed

    Xiao, Feng; Simcik, Matt F; Gulliver, John S

    2012-01-01

    As a persistent, bioaccumulative, and toxic organic pollutant, perfluorooctane sulfonate (PFOS) has been found ubiquitously in the environment, including in tap water. For the first time, we studied PFOS sorption from water to foods (nine commonly consumed vegetables, three meats, and cereals) at two temperatures to estimate the daily intake of PFOS attributable to cooking and food preparation. The values of the food water-distribution coefficient (KF/W, l/kg) of PFOS ranged from 7 to 19 l/kg for most vegetables and from 19 to 38 l/kg for meats. Celery exhibited the highest affinity toward PFOS (KF/W=39.8±3.4 l/kg), whereas onions showed the lowest affinity toward PFOS (KF/W=1.1±0.4 l/kg). Adding table salt (sodium chloride) greatly increased PFOS sorption in most foods, except for celery and meats. The results indicate that human exposure to PFOS could result from the sorption of PFOS from water to food during food preparation, especially when using table salt. The average daily intake of PFOS through this route was estimated. Furthermore, raw and unprocessed foods (vegetables, meats, and cereals) bought from farmers' markets and grocery stores were basically free of PFOS and other long-chain perfluoroalkyl acids. PMID:21597984

  19. Interfacial dynamic and dilational rheology of polyelectrolyte/surfactant two-component nanoparticle systems at air-water interface

    NASA Astrophysics Data System (ADS)

    Tong, L. J.; Bao, M. T.; Li, Y. M.; Gong, H. Y.

    2014-10-01

    The interfacial characteristics of nanoparticles and consequent inter-particle interactions at the interface are poorly understood. In this work, the interfacial dynamic and corresponding dilational surface rheology of self-assembled polyelectrolyte/surfactant nanoparticles at the air-water interface are characterized. The nanoparticles are prepared from dodecyltrimethylammonium (DTAB) and poly (sodium 4-styrene-sulfonate) (PSS) by mixing them in aqueous solution. The interfacial dynamic characteristics have been carried out by comparing the surface pressure with the dilational rheological response of these nanoparticles at interface. The results indicate that this type of nanoparticles can adsorb at the interface forming a nanoparticle monolayer, which leads to the surface tension decreased markedly. The dependence of surface pressure on time shows the instability and disassembly process of nanoparticles at the interface. On the basis of these observations, it is proposed that the nanoparticles undergo a dynamic process that interface induced nanoparticles disassembly into DTAB/PSS complexes. The presence of PSS in the subphase can promote the process of nanoparticles disassembly. A transition point in dilational elasticity and viscosity response of the nanoparticles versus oscillation frequency further validate the micro dynamic process of nanoparticles and the formation of polyelectrolyte/surfactant complex monolayer at the interface.

  20. The effect of guanidinium functionalization on the structural properties and anion affinity of polyelectrolyte multilayers.

    PubMed

    Cao, Zheng; Gordiichuk, Pavlo I; Loos, Katja; Sudhölter, Ernst J R; de Smet, Louis C P M

    2016-02-01

    Poly(allylamine hydrochloride) (PAH) is chemically functionalized with guanidinium (Gu) moieties in water at room temperature. The resulting PAH-Gu is used to prepare polyelectrolyte multilayers (PEMs) with poly(sodium 4-styrene sulfonate) (PSS) via layer-by-layer deposition. The polyelectrolyte (PE) adsorption processes are monitored real-time by optical reflectometry and a quartz crystal microbalance with dissipation monitoring (QCM-D). Compared to the reference PSS/PAH PEMs, the PSS/PAH-Gu PEMs show a lower amount of deposited PE materials, lower wet thickness, higher stability under alkaline conditions and higher rigidity. These differences are rationalized by the additional Gu-SO3(-) interactions, also affecting the conformation of the PE chains in the PEM. The interactions between the PEMs and various sodium salts (NaCl, NaNO3, Na2SO4 and NaH2PO4) are also monitored using QCM-D. From the changes in the frequency, dissipation responses and supportive Reflection Absorption Infrared Spectroscopy it is concluded that Gu-functionalized PEMs absorb more H2PO4(-) compared to the Gu-free reference PEMs. This can be understood by strong interactions between Gu and H2PO4(-), the differences in the anion hydration energy and the anion valency. It is anticipated that compounds like the presented Gu-functionalized PE may facilitate the further development of H2PO4(-) sensors and ion separation/recovery systems. PMID:26658499

  1. Improved Power System Stability Using Backtracking Search Algorithm for Coordination Design of PSS and TCSC Damping Controller.

    PubMed

    Niamul Islam, Naz; Hannan, M A; Mohamed, Azah; Shareef, Hussain

    2016-01-01

    Power system oscillation is a serious threat to the stability of multimachine power systems. The coordinated control of power system stabilizers (PSS) and thyristor-controlled series compensation (TCSC) damping controllers is a commonly used technique to provide the required damping over different modes of growing oscillations. However, their coordinated design is a complex multimodal optimization problem that is very hard to solve using traditional tuning techniques. In addition, several limitations of traditionally used techniques prevent the optimum design of coordinated controllers. In this paper, an alternate technique for robust damping over oscillation is presented using backtracking search algorithm (BSA). A 5-area 16-machine benchmark power system is considered to evaluate the design efficiency. The complete design process is conducted in a linear time-invariant (LTI) model of a power system. It includes the design formulation into a multi-objective function from the system eigenvalues. Later on, nonlinear time-domain simulations are used to compare the damping performances for different local and inter-area modes of power system oscillations. The performance of the BSA technique is compared against that of the popular particle swarm optimization (PSO) for coordinated design efficiency. Damping performances using different design techniques are compared in term of settling time and overshoot of oscillations. The results obtained verify that the BSA-based design improves the system stability significantly. The stability of the multimachine power system is improved by up to 74.47% and 79.93% for an inter-area mode and a local mode of oscillation, respectively. Thus, the proposed technique for coordinated design has great potential to improve power system stability and to maintain its secure operation. PMID:26745265

  2. Improved Power System Stability Using Backtracking Search Algorithm for Coordination Design of PSS and TCSC Damping Controller

    PubMed Central

    Niamul Islam, Naz; Hannan, M. A.; Mohamed, Azah; Shareef, Hussain

    2016-01-01

    Power system oscillation is a serious threat to the stability of multimachine power systems. The coordinated control of power system stabilizers (PSS) and thyristor-controlled series compensation (TCSC) damping controllers is a commonly used technique to provide the required damping over different modes of growing oscillations. However, their coordinated design is a complex multimodal optimization problem that is very hard to solve using traditional tuning techniques. In addition, several limitations of traditionally used techniques prevent the optimum design of coordinated controllers. In this paper, an alternate technique for robust damping over oscillation is presented using backtracking search algorithm (BSA). A 5-area 16-machine benchmark power system is considered to evaluate the design efficiency. The complete design process is conducted in a linear time-invariant (LTI) model of a power system. It includes the design formulation into a multi-objective function from the system eigenvalues. Later on, nonlinear time-domain simulations are used to compare the damping performances for different local and inter-area modes of power system oscillations. The performance of the BSA technique is compared against that of the popular particle swarm optimization (PSO) for coordinated design efficiency. Damping performances using different design techniques are compared in term of settling time and overshoot of oscillations. The results obtained verify that the BSA-based design improves the system stability significantly. The stability of the multimachine power system is improved by up to 74.47% and 79.93% for an inter-area mode and a local mode of oscillation, respectively. Thus, the proposed technique for coordinated design has great potential to improve power system stability and to maintain its secure operation. PMID:26745265

  3. Nitric Acid Dehydration Using Perfluoro Carboxylate and Mixed Sulfonate/Carboxylate Membranes

    SciTech Connect

    Ames, Richard L.

    2004-09-01

    Perfluoro ionomer membranes are tetrafluoro ethylene-based materials with microheterogeneous structures consisting of a hydrophobic polymer backbone and a hydrophilic side-chain cluster region. Due to the ionomer cluster morphology, these films exhibit unique transport properties. Recent investigations with perfluoro sulfonate and perfluoro sulfonate/carboxylate composite polymers have demonstrated their value in the dehydration of nitric acid and they show potential as an alternative to conventional, energy intensive unit operations in the concentration of acid feeds. As a result, investigations were conducted to determine the feasibility of using pure perfluoro carboxylate and mixed perfluoro sulfonate/carboxylate films for the dehydration of nitric acid because of the speculation of improved water selectivity of the carboxylate pendant chain. During the first phase of these investigations the effort was focused on generating a thin, solution cast perfluoro carboxylate ionomer film, to evaluate the general, chemical and physical characteristics of the polymer, and to assess the material's aqueous transport performance (flux and nitrate separation efficiencies) in pervaporation and high-pressure environments. Results demonstrated that generating robust solution-cast films was difficult yet a number of membranes survived high trans-membrane pressures up to 700 psig. General characterization of the solution cast product showed reduced ion exchange capacities when compared with thicker, ''as received'' perfluoro carboxylate and similar sulfonate films. Small angle x-ray scattering analysis results suggested that the solution cast carboxylate films contained a small fraction of sulfonate terminated side-chains. Aqueous transport experimentation showed that permeate fluxes for both pure water and nitric acid were approximately two orders of magnitude smaller for the carboxylate solution cast membranes when compared to their sulfonate counterparts of similar thickness

  4. Ag (I)-based 2D metal frameworks with helical structures decorated by the homochiral camphor-10-sulfonic acid

    NASA Astrophysics Data System (ADS)

    Guo, Peng; Wang, Jing; Wang, Jun; Pan, Daocheng; Xu, Guohai

    2010-12-01

    Two two-dimension homochiral Ag (I) metal frameworks constructed from enantiopure camphor-10-sulfonic acid and hexamethylenetetramine have been synthesized at the room temperature. These two complexes with (6, 3) topology decorated by the homochiral camphor-10-sulfonic acid possess the unique helical structures. The result of Circular Dichroism (CD) spectroscopy confirms that the bulk materials are homochiral and also indicates the handedness of the single crystals can be controlled by the chirality of the camphor-10-sulfonic acid.

  5. Surface modification of carbon fibers by a polyether sulfone emulsion sizing for increased interfacial adhesion with polyether sulfone

    NASA Astrophysics Data System (ADS)

    Yuan, Haojie; Zhang, Shouchun; Lu, Chunxiang

    2014-10-01

    Interests on carbon fiber-reinforced thermoplastic composites are growing rapidly, but the challenges with poor interfacial adhesion have slowed their adoption. In this work, a polyether sulfone (PES) emulsion sizing was prepared successfully for increased interfacial adhesion of carbon fiber/PES composites. To obtain a high-quality PES emulsion sizing, the key factor, emulsifier concentration, was studied by dynamic light scattering technique. The results demonstrated that the suitable weight ratio of PES to emulsifier was 8:3, and the resulting PES emulsion sizing had an average particle diameter of 117 nm and Zeta potential of -52.6 mV. After sizing, the surface oxygen-containing functional groups, free energy and wettability of carbon fibers increased significantly, which were advantageous to promote molecular-level contact between carbon fiber and PES. Finally, short beam shear tests were performed to evaluate the interfacial adhesion of carbon fiber/PES composites. The results indicated that PES emulsion sizing played a critical role for the enhanced interfacial adhesion in carbon fiber/PES composites, and a 26% increase of interlaminar shear strength was achieved, because of the improved fiber surface wettability and interfacial compatibility between carbon fiber and PES.

  6. Advances in membrane materials: desalination membranes based on directly copolymerized disulfonated poly(arylene ether sulfone) random copolymers.

    PubMed

    Xie, Wei; Park, Ho-Bum; Cook, Joseph; Lee, Chang Hyun; Byun, Gwangsu; Freeman, Benny D; McGrath, James E

    2010-01-01

    The water and salt transport properties of chlorine tolerant disulfonated poly(arylene ether sulfone) (BPS) copolymers have been characterized. Cast BPS membranes of both salt form and acid form with sulfonation levels from 20% to 40% were investigated. Water permeability of BPS films increases more than one order of magnitude as sulfonation level increases from 20% to 40%, while the salt permeability of the corresponding membranes increases two orders of magnitude. Moderate salt rejection (98.2%) was achieved by a BPS salt form membrane with a sulfonation level of 20%.

  7. [Studies for analyzing restricted ingredients such as phenylbenzoimidazole sulfonic acid].

    PubMed

    Tokunaga, Hiroshi; Mori, Kenichiro; Onuki, Nahomi; Nosaka, Tomio; Doi, Kayo; Sakaguchi, Hiroshi; Fujii, Makiko; Takano, Katuhiro; Hayashi, Masato; Yoshizawa, Kenichi; Shimamura, Kimio; Sato, Nobuo

    2006-01-01

    Phenylbenzoimidazol sulfonic acid (PBS) is a kind of sunscreens in cosmetics and is nominated as the restricted ingredients in cosmetics in Japanese Pharmaceutical Affairs Act. So the analytical method for PBS was investigated by HPLC. 1.0 g of the lotions with 1.0% PBS was exactly weighed, put into a 50-mL volumetric flask. Water was added to make exactly 50 mL and this mixture was used as the sample solution. On the other hand, 1.0 g of the creams with 1.0% PBS was exactly weighed, put into a beaker. After adding 1 mL of tetrahydrofuran and dissolving the cream, that mixture was transferred to a 50-mL volumetric flask. And then the beaker was rinsed with 1 mL of tetrahydrofuran and the rinsed solution was put together into the volumetric flask. After adding water to the volumetric flask to make exactly 50 mL, this mixture was used as the sample solution. If necessary, the mixture was filtrated with a membrane filter (0.45 microm). 5.0 mL of the sample solution was pipetted and put into a 200-mL volumetric flask. After adding water to make exactly 200 mL, 20 microL of this solution was analyzed by HPLC using the ODS column (CAPCELL PAK C18 column, 4.6 mm i.d. x 250 mm), the mixture of 40 mmol/L acetic buffer (pH 3.4) and acetonitrile (3:1) with 0.8 mmol/L dodecyltrimethyl ammonium bromide and the detection wavelength of 305 nm. The working curve from 0.5 to 20.0 microg/mL showed a linear line between the concentrations of PBS and the peak areas. There was no interference of peak of PBS from the lotion and cream.

  8. Fate of linear alkylbenzene sulfonate (LAS) in activated sludge plants.

    PubMed

    Temmink, H; Klapwijk, Bram

    2004-02-01

    Monitoring data were collected in a pilot-scale municipal activated sludge plant to assess the fate of the C12-homologue of linear alkyl benzene sulfonate (LAS-C12). The pilot-plant was operated at influent LAS-C12 concentrations between 2 and 12 mg l(-1) and at sludge retention times of 10 and 27 days. Effluent and waste sludge concentrations varied between 5 and 10 microg l(-1) and between 37 and 69 microg g(-1) VSS, respectively. In the sludge samples only 2-8% was present as dissolved LAS-C12, whereas the remaining 92-98% was found to be adsorbed to the sludge. In spite of this high degree of sorption, more than 99% of the LAS-C12 load was removed by biodegradation, showing that not only the soluble fraction but also the adsorbed fraction of LAS-C12 is readily available for biodegradation. Sorption and biodegradation of LAS-C12 were also investigated separately. Sorption was an extremely fast and reversible process and could be described by a linear isotherm with a partition coefficient of 3.2 l g(-1) volatile suspended solids. From the results of biodegradation kinetic tests it was concluded that primary biodegradation of LAS-C12 cannot be described by a (growth) Monod model, but a secondary utilisation model should be used instead. The apparent affinity of the sludge to biodegrade LAS-C12 increased when the sludge was loaded with higher influent concentrations of LAS-C12.

  9. Grafting titanium nitride surfaces with sodium styrene sulfonate thin films.

    PubMed

    Zorn, Gilad; Migonney, Véronique; Castner, David G

    2014-09-01

    The importance of titanium nitride lies in its high hardness and its remarkable resistance to wear and corrosion, which has led to its use as a coating for the heads of hip prostheses, dental implants and dental surgery tools. However, the usefulness of titanium nitride coatings for biomedical applications could be significantly enhanced by modifying their surface with a bioactive polymer film. The main focus of the present work was to graft a bioactive poly(sodium styrene sulfonate) (pNaSS) thin film from titanium nitride surfaces via a two-step procedure: first modifying the surface with 3-methacryloxypropyltrimethoxysilane (MPS) and then grafting the pNaSS film from the MPS modified titanium through free radical polymerization. X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS) were used after each step to characterize success and completeness of each reaction. The surface region of the titanium nitride prior to MPS functionalization and NaSS grafting contained a mixture of titanium nitride, oxy-nitride, oxide species as well as adventitious surface contaminants. After MPS functionalization, Si was detected by XPS, and characteristic MPS fragments were detected by ToF-SIMS. After NaSS grafting, Na and S were detected by XPS and characteristic NaSS fragments were detected by ToF-SIMS. The XPS determined thicknesses of the MPS and NaSS overlayers were ∼1.5 and ∼1.7 nm, respectively. The pNaSS film density was estimated by the toluidine blue colorimetric assay to be 260 ± 70 ng/cm(2).

  10. Mechanisms for selective toxicity of fipronil insecticide and its sulfone metabolite and desulfinyl photoproduct.

    PubMed

    Hainzl, D; Cole, L M; Casida, J E

    1998-12-01

    Fipronil, an N-phenylpyrazole with a trifluoromethylsulfinyl substituent, initiated the second generation of insecticides acting at the gamma-aminobutyric acid (GABA) receptor to block the chloride channel. The first generation includes the polychlorocycloalkanes alpha-endosulfan and lindane. In this study, we examine the mechanisms for selective toxicity of the sulfoxide fipronil and its sulfone metabolite and desulfinyl photoproduct relative to their target site interactions in vitro and ex vivo and the importance in fipronil action of biooxidation to the sulfone. Differences in GABA receptor sensitivity, assayed by displacement of 4'-ethynyl-4-n-[2, 3-3H2]propylbicycloorthobenzoate ([3H]EBOB) from the noncompetitive blocker site, appear to be a major factor in fipronil being much more toxic to the insects (housefly and fruit fly) than to the vertebrates (humans, dogs, mice, chickens, quail, and salmon) examined; in insects, the IC50s range from 3 to 12 nM for fipronil and its sulfone and desulfinyl derivatives, while in vertebrates, the IC50 average values are 1103, 175, and 129 nM for fipronil, fipronil sulfone, and desulfinyl fipronil, respectively. The insect relative to the vertebrate specificity decreases in the following order: fipronil > lindane > desulfinyl fipronil > fipronil sulfone > alpha-endosulfan. Ex vivo inhibition of [3H]EBOB binding in mouse brain is similar for fipronil and its sulfone and desulfinyl derivatives at the LD50 dose, but surprisingly, at higher doses fipronil can be lethal without detectably blocking the [3H]EBOB site. The P450 inhibitor piperonyl butoxide, acting in houseflies, increases the metabolic stability and effectiveness of fipronil and the sulfone but not those of the desulfinyl compound, and in mice it completely blocks the sulfoxide to sulfone conversion without altering the poisoning. Thus, the selective toxicity of fipronil and fipronil-derived residues is due in part to the higher potency of the parent compound at

  11. Enhanced osteoblast-like cell adhesion and proliferation using sulfonate-bearing polymeric scaffolds.

    PubMed

    Chaterji, Somali; Gemeinhart, Richard A

    2007-12-15

    Orthopedic malfunction, degeneration, or damage remains a serious healthcare issue despite advances in medical technology. Proactive extracellular matrix (ECM)-mimetic scaffolds are being researched to orchestrate the activation of diverse osteogenic signaling cascades, facilitating osteointegration. We hypothesized that sulfonated functionalities incorporated into synthetic hydrogels would simulate anionic, sulfate-bearing proteoglycans, abundant in the ECM. Using this rationale, we successfully developed differentially sulfonated hydrogels, polymerizing a range of sulfopropyl acrylate potassium-acrylamide (SPAK-AM) mole ratios as monomer feeds under room temperature conditions. For anchorage-dependent cells, such as osteoblasts, adhesion is a critical prerequisite for subsequent osteointegration and cell specialization. The introduction of the sulfonated monomer, SPAK, resulted in favorable uptake of serum proteins with proportional increase in adhesion and proliferation rates of model cell lines, which included NIH/3T3 fibroblasts, MG-63 osteoblasts, and MC3T3-E1 subclone 4 preosteoblasts. In fact, higher proportions of sulfonate content (pSPAK75, pSPAK100) exhibited comparable or even higher degrees of adhesion and proliferation, relative to commercial grade tissue culture polystyrene in vitro. These results indicate promising potentials of sulfonated ECM-mimetic hydrogels as potential osteogenic tissue engineering scaffolds. PMID:17584889

  12. [New synthesis of the anticoagulant pentasaccharide idraparinux and preparation of its analogues containing sulfonic acid moieties].

    PubMed

    Herczeg, Mihály

    2012-01-01

    Two novel synthetic pathways were elaborated for the preparation of idraparinux, a heparin-related fully O-sulfated, O-methylated anticoagulant pentasaccharide. Both methods based upon a [2+3] block synthesis utilizing the same trisaccharide acceptor which was coupled to either a uronic acid disaccharide donor or its nonoxidized precursor. Two bioisosteric sulfonic acid analogues of idraparinux were also prepared, in which two or three primary sulfate esters were replaced by sodium-sulfonatomethyl moieties. The sulfonic acid groups were formed on a monosaccharide level and the obtained carbohydrate sulfonic acid esters were found to be excellent donors and acceptors in the glycosylation reactions. The disulfonic-acid analogue was prepared in a [2+3] block synthesis by using a trisaccharide disulfonic acid as an acceptor and a glucuronide disaccharide as a donor. For the synthesis of the pentasaccharide trisulfonic acid, a more-efficient approach, which involved elongation of the trisaccharide acceptor with a non-oxidized precursor of the glucuronic acid followed by post-glycosidation oxidation at the tetrasaccharide level and a subsequent [1+4] coupling reaction, was elaborated. In vitro evaluation of the anticoagulant activity of the reference compound idraparinux and the new sulfonic acid derivatives revealed that the disulfonate analogue inhibited the blood-coagulation-proteinase factor Xa with outstanding efficacy; however, the introduction of the third sulfonic acid moiety resulted in a notable decrease in the anti-Xa activity.

  13. Copoly(arlene ether)s containing pendant sulfonic acid groups as proton exchange membrane

    SciTech Connect

    Kim, Yu Seung; Kim, Dae Sik; Robertson, Gilles; Guiver, Michael

    2008-01-01

    A copoly(arylene ether) (PAE) with high fluorine content and a copoly(arylene ether nitrile) (PAEN) with high nitrile content, each containing pendant phenyl sulfonic acids were synthesized. The P AE and PAEN were prepared from decafluorobiphenyl (DFBP) and difluorobenzonitrile (DFBN) respectively, by polycondensation with 2-phenylhydroquinone (PHQ) by conventional aromatic nucleophilic substitution reactions. The sulfonic acid groups were introduced by mild post-sulfonation exclusively on the para-position of the pendant phenyl ring in PHQ. The membrane properties of the resulting sulfonated copolymers sP AE and sP AEN were compared for fuel cell applications. The copolymers sPAE and sPAEN, each having a degree of sulfonation (DS) of 1.0 had high ion exchange capacities (IEC{sub v}(wet) (volume-based, wet state)) of 1.77 and 2.55 meq./cm{sup 3}, high proton conductivities of 135.4 and 140.1 mS/cm at 80 C, and acceptable volume-based water uptake of 44.5-51.9 vol% at 80 C, respectively, compared to Nafion. The data points of these copolymer membranes are located in the area of outstanding properties in the trade-off plot of alternative hydrocarbon polyelectrolyte membranes (PEM) for the relationship between proton conductivity versus water uptake (weight based or volume based). Furthermore, the relative selectivity derived from proton conductivity and methanol permeability is higher than that of Nafion.

  14. The enhancement of PCR amplification by low molecular-weight sulfones.

    PubMed

    Chakrabarti, R; Schutt, C E

    2001-08-22

    DNA amplification by polymerase chain reaction (PCR) is frequently complicated by the problems of low yield and specificity, especially when the GC content of the target sequence is high. A common approach to the optimization of such reactions is the addition of small quantities of certain organic chemicals, such as dimethylsulfoxide (DMSO), betaine, polyethylene glycol and formamide, to the reaction mixture. Even in the presence of such additives, however, the amplification of GC-rich templates is often ineffective. In this paper, we introduce a novel class of PCR-enhancing compounds, the low molecular-weight sulfones, that are effective in the optimization of high GC template amplification. We describe here the results of an extensive structure-activity investigation in which we studied the effects of a series of six different sulfones on PCR amplification. We identify two sulfones, sulfolane and methyl sulfone, that are especially potent enhancers of high GC template amplification, and show that these compounds often outperform DMSO and betaine, two of the most effective PCR enhancers currently used. We conclude with a brief discussion of the role that the sulfone functional group may play in such enhancement.

  15. Tin Coatings Electrodeposited from Sulfonic Acid-Based Electrolytes: Tribological Behavior

    NASA Astrophysics Data System (ADS)

    Bengoa, L. N.; Tuckart, W. R.; Zabala, N.; Prieto, G.; Egli, W. A.

    2015-06-01

    A high efficiency methane sulfonic acid electrolyte used for tin electrodeposition was studied, and the properties of the resulting deposits were compared to those of tin coatings obtained from an industrial phenol sulfonic acid electrolyte. Cyclic voltammetry was used to study the effect of organic additives on the reduction process to define the composition of the electrolytic bath. Thick tin electrodeposits were obtained on rotating cylinder steel electrodes, and their surface morphology, preferred crystal orientation, surface roughness, micro hardness, and tribological behavior were measured. Smooth, adherent, and bright tin coatings were obtained from the methane sulfonic acid electrolyte, which differed in morphology and texture from tin electrodeposited from the industrial bath. Influence of organic additives on preferred crystal orientation of the coatings was found to be stronger than changing the supporting sulfonic acid type. Tribological tests showed that the two types of deposits have a similar coefficient of friction. However, tin coatings obtained from methane sulfonic electrolytes presented a lower wear resistance and underwent galling at lower loads.

  16. [New synthesis of the anticoagulant pentasaccharide idraparinux and preparation of its analogues containing sulfonic acid moieties].

    PubMed

    Herczeg, Mihály

    2012-01-01

    Two novel synthetic pathways were elaborated for the preparation of idraparinux, a heparin-related fully O-sulfated, O-methylated anticoagulant pentasaccharide. Both methods based upon a [2+3] block synthesis utilizing the same trisaccharide acceptor which was coupled to either a uronic acid disaccharide donor or its nonoxidized precursor. Two bioisosteric sulfonic acid analogues of idraparinux were also prepared, in which two or three primary sulfate esters were replaced by sodium-sulfonatomethyl moieties. The sulfonic acid groups were formed on a monosaccharide level and the obtained carbohydrate sulfonic acid esters were found to be excellent donors and acceptors in the glycosylation reactions. The disulfonic-acid analogue was prepared in a [2+3] block synthesis by using a trisaccharide disulfonic acid as an acceptor and a glucuronide disaccharide as a donor. For the synthesis of the pentasaccharide trisulfonic acid, a more-efficient approach, which involved elongation of the trisaccharide acceptor with a non-oxidized precursor of the glucuronic acid followed by post-glycosidation oxidation at the tetrasaccharide level and a subsequent [1+4] coupling reaction, was elaborated. In vitro evaluation of the anticoagulant activity of the reference compound idraparinux and the new sulfonic acid derivatives revealed that the disulfonate analogue inhibited the blood-coagulation-proteinase factor Xa with outstanding efficacy; however, the introduction of the third sulfonic acid moiety resulted in a notable decrease in the anti-Xa activity. PMID:23230650

  17. Polymer electrolyte membranes from fluorinated polyisoprene-block-sulfonated polystyrene: Membrane structure and transport properties

    SciTech Connect

    Sodeye, Akinbode; Huang, Tianzi; Gido, Samuel; Mays, Jimmy

    2011-01-01

    With a view to optimizing morphology and ultimately properties, membranes have been cast from relatively inexpensive block copolymer ionomers of fluorinated polyisoprene-block-sulfonated polystyrene (FISS) with various sulfonation levels, in both the acid form and the cesium neutralized form. The morphology of these membranes was characterized by transmission electron microscopy and ultra-small angle X-ray scattering, as well as water uptake, proton conductivity and methanol permeability within the temperature range from 20 to 60 C. Random phase separated morphologies were obtained for all samples except the cesium sample with 50 mol% sulfonation. The transport properties increased with increasing degree of sulfonation and temperature for all samples. The acid form samples absorbed more water than the cesium samples with a maximum swelling of 595% recorded at 60 C for the acid sample having 50 mol% sulfonation. Methanol permeability for the latter sample was more than an order of magnitude less than for Nafion 112 but so was the proton conductivity within the plane of the membrane at 20 C. Across the plane of the membrane this sample had half the conductivity of Nafion 112 at 60 C.

  18. Poly(thieno[3,4-b]thiophene)-poly(styrene sulfonate): a low band gap, water dispersible conjugated polymer.

    PubMed

    Lee, Byoungchul; Seshadri, Venkataramanan; Sotzing, Gregory A

    2005-11-01

    Herein we report the oxidative chemical polymerization of thieno[3,4-b]thiophene (T34bT) using several different oxidants including ferric sulfate, ammonium persulfate, and hydrogen peroxide in the presence of poly(styrenesulfonic acid) in water and properties of the resulting poly(thieno[3,4-b]thiophene)-poly(styrenesulfonic acid) (PT34bT-PSS) dispersion. The PT34bT-PSS is rendered a colloidal dispersion in water with a particle size diameter ranging between 180 and 220 nm depending on the oxidant used for polymerization. PT34bT-PSS films have band gaps of ca. 1 eV (1260 nm) as determined by the onset of the pi to pi transition from the vis-NIR spectrum with absorption maxima ranging from 1.4 eV (912 nm) to 1.7 eV (724 nm). The neutral and oxidized forms of PT34bT-PSS prepared from ferric sulfate dispersed in water were blue and lime green, respectively, whereas the neutral and oxidized forms of PT34bT-PSS prepared from ammonium persulfate and hydrogen peroxide were blue and blue-green, respectively. Spectral properties of the PT34bT-PSS dispersion can be tuned by the combination of oxidants. PT34bT-PSS films showed ca. 100% cation dominant ion transport behavior as determined by electrochemical gravimetry with each charge-discharge cycle and the doping level of the polymer was calculated to be 26%. Electrical conductivities for these polymers were found to be dependent on chemical oxidants used and varied from 10(-2) to 10(-4) S/cm. PMID:16262354

  19. Facile construction of vertically aligned ZnO nanorod/PEDOT:PSS hybrid heterojunction-based ultraviolet light sensors: efficient performance and mechanism

    NASA Astrophysics Data System (ADS)

    Ranjith, K. S.; Rajendra Kumar, R. T.

    2016-03-01

    We demonstrate a simple, planar manufacturing process-compatible fabrication of highly efficient UV sensors based on a hybrid heterojunction of an array of vertically aligned ZnO nanorods (NRs) and PEDOT:PSS. The ZnO NR array was grown by the solution growth process and the aspect ratio (length 1 to 4 μm, diameter ˜80 nm) of the rods was controlled by varying the growth time. UV sensors based on (i) naked ZnO NRs and (ii) ZnO NR/PEDOT:PSS heterojunctions were fabricated and tested. The UV sensitivity of bare ZnO NRs was found to increase with increasing aspect ratio of the NRs due to the increase in the photogenerated charge carriers as the fraction of material interacting with the light increases. Under 5 V bias, naked ZnO NR arrays showed a photocurrent of 8.84 × 10-5 A, a responsivity of 0.538 A W-1 and a sensitivity of 4.80 under UV (λ = 256 nm, 130 μW) illumination. ZnO NR/PEDOT:PSS hybrid heterojunctions showed diode-like behavior with a leakage current less than 2.54 × 10-8 A at -5 V and forward turn-on voltage of 1.1 V. ZnO NR/polymer-based hybrid heterojunctions show a photocurrent of 6.74 × 10-4 A, responsivity of 5.046 A W-1 and excellent sensitivity of 37.65 under UV (λ = 256 nm, 130 μW) illumination. Compared with bare ZnO NR arrays, the ZnO NR/polymer heterojunction device shows responsivity enhanced by a factor of 10, sensitivity enhanced by a factor of 8 and faster rise and decay time. The enhanced performance may be due to effective charge separation guided by the built-in potential formed at the interface between ZnO NRs and PEDOT:PSS.

  20. PEDOT:PSS-Based Piezo-Resistive Sensors Applied to Reinforcement Glass Fibres for in Situ Measurement during the Composite Material Weaving Process

    PubMed Central

    Trifigny, Nicolas; Kelly, Fern M.; Cochrane, Cédric; Boussu, François; Koncar, Vladan; Soulat, Damien

    2013-01-01

    The quality of fibrous reinforcements used in composite materials can be monitored during the weaving process. Fibrous sensors previously developed in our laboratory, based on PEDOT:PSS, have been adapted so as to directly measure the mechanical stress on fabrics under static or dynamic conditions. The objective of our research has been to develop new sensor yarns, with the ability to locally detect mechanical stresses all along the warp or weft yarn. This local detection is undertaken inside the weaving loom in real time during the weaving process. Suitable electronic devices have been designed in order to record in situ measurements delivered by this new fibrous sensor yarn. PMID:23959238

  1. PEDOT:PSS-based piezo-resistive sensors applied to reinforcement glass fibres for in situ measurement during the composite material weaving process.

    PubMed

    Trifigny, Nicolas; Kelly, Fern M; Cochrane, Cédric; Boussu, François; Koncar, Vladan; Soulat, Damien

    2013-08-16

    The quality of fibrous reinforcements used in composite materials can be monitored during the weaving process. Fibrous sensors previously developed in our laboratory, based on PEDOT:PSS, have been adapted so as to directly measure the mechanical stress on fabrics under static or dynamic conditions. The objective of our research has been to develop new sensor yarns, with the ability to locally detect mechanical stresses all along the warp or weft yarn. This local detection is undertaken inside the weaving loom in real time during the weaving process. Suitable electronic devices have been designed in order to record in situ measurements delivered by this new fibrous sensor yarn.

  2. Synthesis of Unsymmetrical Sulfides and Their Oxidation to Sulfones to Discover Potent Antileishmanial Agents.

    PubMed

    Dar, Ajaz A; Enjamuri, Nagasuresh; Shadab, Md; Ali, Nahid; Khan, Abu T

    2015-11-01

    Unsymmetrical sulfides were first synthesized using combinations of a 1,3-dicarbonyl, an aromatic aldehyde and a thiol in the presence of 10 mol % ethanolic piperidine. These sulfides derivatives were subsequently converted into corresponding sulfones via oxidation in the presence of m-chloroperoxybenzoic acid (m-CPBA) at ice-bath to room temperature. The former reaction was achieved at room temperature through one-pot three-component. The later was obtained in good yields using mild reaction conditions with flexibility in choice from a range of substrates. The antimicrobial properties of the newly synthesized sulfone derivatives were investigated against the protozoan parasite, Leishmania donovani, a causative agent of visceral leishmaniasis (VL). Nine sulfone derivatives were found to be efficacious and exhibited significant antimicrobial activity. Further, these compounds were nontoxic on murine peritoneal macrophages thus eliminating potential cytoxicity in the host cells. These compounds may be indicated as potential leads in the treatment of visceral leishmaniasis. PMID:26441303

  3. Synthesis of porous sulfonated carbon as a potential adsorbent for phenol wastewater.

    PubMed

    Prabhu, Azhagapillai; Al Shoaibi, Ahmed; Srinivasakannan, C

    2015-01-01

    The work reports a facile synthesis procedure for preparation of porous sulfonated carbons and its suitability for adsorption of phenol. The sulfonated carbon was synthesized utilizing a simplified, single-step, shorter duration process by sulfonation, dehydration and carbonization of sucrose in sulfuric acid and tetraethylorthosilicate. The surface and internal structures of the adsorbents were characterized utilizing various characterization techniques to understand the porous nature and surface functional groups of the porous matrix. Adsorption capacity was found to be highest for the sample heat treated at 600 °C, with the maximum adsorption capacity of 440 mg/g at 30 °C. The adsorption isotherms were tested with the Freundlich and Langmuir adsorption isotherms models to identify the appropriate adsorption mechanism.

  4. Sulfonated dyes attenuate the toxic effects of beta-amyloid in a structure-specific fashion.

    PubMed

    Pollack, S J; Sadler, I I; Hawtin, S R; Tailor, V J; Shearman, M S

    1995-09-15

    We recently reported that several sulfate-containing glycosaminoglycans, a class of compounds associated with the beta-amyloid plaques of Alzheimer's disease, attenuate the toxic effects of beta-amyloid fragments beta 25-35 and beta 1-40. The amyloid-binding sulfonated dye Congo Red was shown to have a similar effect. Using two clonal cell lines, we now demonstrate that several sulfonated dyes attenuate beta-amyloid toxicity and that the protective effect appears specific for compounds whose sulfonate groups can interact with the beta-pleated structure of aggregated amyloid. These results suggest that by binding beta-amyloid these compounds may prevent toxic interactions of the peptide with cells.

  5. Nuclear Magnetic Resonance Identification of New Sulfonic Acid Metabolites of Chloroacetanilide Herbicides

    USGS Publications Warehouse

    Morton, M.D.; Walters, F.H.; Aga, D.S.; Thurman, E.M.; Larive, C.K.

    1997-01-01

    The detection of the sulfonic acid metabolites of the chloroacetanilide herbicides acetochlor, alachlor, butachlor, propachlor, and, more recently, metolachlor in surface and ground water suggests that a common mechanism for dechlorination exists via the glutathione conjugation pathway. The identification of these herbicides and their metabolites is important due to growing public awareness and concern about pesticide levels in drinking water. Although these herbicides are regulated, little is known about the fate of their metabolites in soil. The sulfonic acid metabolites were synthesized by reaction of the parent compounds with an excess of sodium sulfite. Acetochlor, alachlor, butachlor, metolachlor, and propachlor and their sulfonic acid metabolites were studied by nuclear magnetic resonance spectroscopy and fast atom bombardment mass spectrometry. This paper provides a direct method for the preparation and characterization of these compounds that will be useful in the analysis and study of chloracetanilide herbicides and their metabolites.

  6. QENS investigation of proton confined motions in hydrated perfluorinated sulfonic membranes and self-assembled surfactants

    NASA Astrophysics Data System (ADS)

    Berrod, Quentin; Lyonnard, Sandrine; Guillermo, Armel; Ollivier, Jacques; Frick, Bernhard; Gébel, Gérard

    2015-01-01

    We report on QuasiElastic Neutron Scattering (QENS) investigations of the dynamics of protons and water molecules confined in nanostructured perfluorinated sulfonic acid (PFSA) materials, namely a commercial Aquivion membrane and the perfluorooctane sulfonic acid (PFOS) surfactant. The former is used as electrolyte in low-temperature fuel cells, while the latter forms mesomorphous self-assembled phases in water. The dynamics was investigated as a function of the hydration level, in a wide time range by combining time-of-flight and backscattering incoherent QENS experiments. Analysis of the quasielastic broadening revealed for both systems the existence of localized translational diffusive motions, fast rotational motions and slow hopping of protons in the vicinity of the sulfonic charges. The characteristic times and diffusion coefficients have been found to exhibit a very similar behaviour in both membrane and surfactant structures. Our study provides a comprehensive picture of the proton motion mechanisms and the dynamics of confined water in model and real PFSA nanostructures.

  7. Improving the Serum Stability of Site-Specific Antibody Conjugates with Sulfone Linkers

    PubMed Central

    2015-01-01

    Current routes for synthesizing antibody–drug conjugates commonly rely on maleimide linkers to react with cysteine thiols. However, thioether exchange with metabolites and serum proteins can compromise conjugate stability and diminish in vivo efficacy. We report the application of a phenyloxadiazole sulfone linker for the preparation of trastuzumab conjugates. This sulfone linker site-specifically labeled engineered cysteine residues in THIOMABs and improved antibody conjugate stability in human plasma at sites previously shown to be labile for maleimide conjugates. Similarly, sulfone conjugation with selenocysteine in an anti-ROR1 scFv-Fc improved human plasma stability relative to maleimide conjugation. Kinetically controlled labeling of a THIOMAB containing two cysteine substitutions was also achieved, offering a strategy for producing antibody conjugates with expanded valency. PMID:25099687

  8. Mechanoassisted Synthesis of Sulfonated Covalent Organic Frameworks with High Intrinsic Proton Conductivity.

    PubMed

    Peng, Yongwu; Xu, Guodong; Hu, Zhigang; Cheng, Youdong; Chi, Chenglong; Yuan, Daqiang; Cheng, Hansong; Zhao, Dan

    2016-07-20

    It is challenging to introduce pendent sulfonic acid groups into modularly built crystalline porous frameworks for intrinsic proton conduction. Herein, we report the mechanoassisted synthesis of two sulfonated covalent organic frameworks (COFs) possessing one-dimensional nanoporous channels decorated with pendent sulfonic acid groups. These COFs exhibit high intrinsic proton conductivity as high as 3.96 × 10(-2) S cm(-1) with long-term stability at ambient temperature and 97% relative humidity (RH). In addition, they were blended with nonconductive polyvinylidene fluoride (PVDF) affording a series of mixed-matrix membranes (MMMs) with proton conductivity up to 1.58 × 10(-2) S cm(-1) and low activation energy of 0.21 eV suggesting the Grotthuss mechanism for proton conduction. Our study has demonstrated the high intrinsic proton conductivity of COFs shedding lights on their wide applications in proton exchange membranes.

  9. Mechanoassisted Synthesis of Sulfonated Covalent Organic Frameworks with High Intrinsic Proton Conductivity.

    PubMed

    Peng, Yongwu; Xu, Guodong; Hu, Zhigang; Cheng, Youdong; Chi, Chenglong; Yuan, Daqiang; Cheng, Hansong; Zhao, Dan

    2016-07-20

    It is challenging to introduce pendent sulfonic acid groups into modularly built crystalline porous frameworks for intrinsic proton conduction. Herein, we report the mechanoassisted synthesis of two sulfonated covalent organic frameworks (COFs) possessing one-dimensional nanoporous channels decorated with pendent sulfonic acid groups. These COFs exhibit high intrinsic proton conductivity as high as 3.96 × 10(-2) S cm(-1) with long-term stability at ambient temperature and 97% relative humidity (RH). In addition, they were blended with nonconductive polyvinylidene fluoride (PVDF) affording a series of mixed-matrix membranes (MMMs) with proton conductivity up to 1.58 × 10(-2) S cm(-1) and low activation energy of 0.21 eV suggesting the Grotthuss mechanism for proton conduction. Our study has demonstrated the high intrinsic proton conductivity of COFs shedding lights on their wide applications in proton exchange membranes. PMID:27385672

  10. Polymer electrolyte membranes from fluorinated polyisoprene-block-sulfonated polystyrene: Structural evolution with hydration and heating

    SciTech Connect

    Sodeye, Akinbode; Huang, Tianzi; Gido, Samuel; Mays, Jimmy

    2011-01-01

    Small-angle neutron scattering (SANS) and ultra-small-angle X-ray scattering (USAXS) have been used to study the structural changes in fluorinated polyisoprene/sulfonated polystyrene (FISS) diblock copolymers as they evolved from the dry state to the water swollen state. A dilation of the nanometer-scale hydrophilic domains has been observed as hydration increased, with greater dilation occurring in the more highly sulfonated samples or upon hydration at higher temperatures. Furthermore, a decrease in the order in these phase separated structures is observed upon swelling. The glass transition temperatures of the fluorinated blocks have been observed to decrease upon hydration of these materials, and at the highest hydration levels, differential scanning calorimetry (DSC) has shown the presence of tightly bound water. A precipitous drop in the mechanical integrity of the 50% sulfonated materials is also observed upon exceeding the glass transition temperature (Tg), as measured by dynamic mechanical analysis (DMA).

  11. Functionalization of overbased calcium sulfonates-synthesis and evaluation of antiwear and extreme-pressure performances

    SciTech Connect

    Delfort, B.; Born, M.; Daoudal, B.

    1995-12-01

    To improve antiwear and extreme-pressure performances of overbased calcium sulfonates, three overbased substrates with different colloidal characteristics were modified by partial neutralization with two sulfur-containing carboxylic acids, dithiodigylcolic acid and 4,4{prime} -(1,3,4-thiadiazole-2,5-diyl) bis (thiabutanoic) acid (DMTD/AA). In this way, six modified overbased calcium sulfonates were prepared. For each product, the colloidal nature of the calcium carboxylate was demonstrated, and all modified and non-modified compounds were evaluated as antiwear and extreme-pressure additives at different concentrations in oil in four-ball tests. The results of this evaluation show that the antiwear performances of basic overbased calcium sulfonates depends on the colloidal structure, while extreme-pressure properties depend on the total calcium carbonate amount in oil. Functionalization significantly enhances the extreme-pressure performances without affecting the initial good antiwear behavior. 20 refs., 9 figs., 4 tabs.

  12. Use of esters of sulfonic acids as anti-sludge agents during the acidizing of formations containing sludging crude oils

    SciTech Connect

    Looney, J.R.; McDougall, L.A.

    1984-04-10

    An anti-sludge agent useful for acid stimulated hydrocarbon containing formations is an ester of sulfonic acid, e.g. monoethoxylated dodecyl benzene sulfonic acid, preferably used in combination with from 0.1 to 2 parts by weight of a surfactant.

  13. Generation of Sulfonyl Radicals from Aryldiazonium Tetrafluoroborates and Sulfur Dioxide: The Synthesis of 3-Sulfonated Coumarins.

    PubMed

    Zheng, Danqing; Yu, Jiyao; Wu, Jie

    2016-09-19

    A catalyst-free approach for the generation of sulfonyl radicals from aryldiazonium tetrafluoroborates in the presence of DABCO⋅(SO2 )2 is realized. The combination of aryldiazonium tetrafluoroborates, DABCO⋅(SO2 )2 , and aryl propiolates affords 3-sulfonated coumarins in good to excellent yields. This tandem reaction process involves radical addition, spirocyclization, and 1,2-migration of esters. Additionally, the in situ diazotization of a number of anilines allows the directional synthesis of desired 3-sulfonated coumarins in a one-pot, two-step process. PMID:27603499

  14. Ruthenium(II)-catalyzed oxidative C-H alkenylations of sulfonic acids, sulfonyl chlorides and sulfonamides.

    PubMed

    Ma, Wenbo; Mei, Ruhuai; Tenti, Giammarco; Ackermann, Lutz

    2014-11-10

    Twofold C-H functionalization of aromatic sulfonic acids was achieved with an in situ generated ruthenium(II) catalyst. The optimized cross-dehydrogenative alkenylation protocol proved applicable to differently substituted arenes and a variety of alkenes, including vinyl arenes, sulfones, nitriles and ketones. The robustness of the ruthenium(II) catalyst was demonstrated by the chemoselective oxidative olefination of sulfonamides as well as sulfonyl chlorides. Mechanistic studies provided support for a reversible, acetate-assisted C-H ruthenation, along with a subsequent olefin insertion.

  15. Synthesis of chlorovinyl sulfones as structural analogs of chalcones and their antiplasmodial activities.

    PubMed

    Dominguez, Jose N; Leon, Caritza; Rodrigues, Juan; Gamboa de Dominguez, Neira; Gut, Jiri; Rosenthal, Philip J

    2009-04-01

    The synthesis of novel chlorovinyl sulfone-like chalcone derivatives and their antimalarial activity against cultured Plasmodium falciparum parasites, hemozoin formation, hemoglobin hydrolysis and murine malaria model are described. Compounds were prepared via Claisen-Schmidt condensation from available chloromethylphenyl sulfones with substituted aldehydes. Antiplasmodial IC(50) activity of these compounds ranged between 0.025 and 10 microM, those that blocked P. falciparum development at low micro molar concentrations were tested in a murine Plasmodium berghei model, and these compounds delayed the progression of malaria but did not eradicate infections. Much effort and attention are needed for discovery and development of new and less toxic antimalarial drugs.

  16. Calorimetric and computational study of 1,4-dithiacyclohexane 1,1-dioxide (1,4-dithiane sulfone).

    PubMed

    Roux, María Victoria; Temprado, Manuel; Jiménez, Pilar; Notario, Rafael; Guzman-Mejía, Ramón; Juaristi, Eusebio

    2006-03-31

    This work reports the enthalpies of formation in the condensed and gas state of 1,4-dithiacyclohexane 1,1-dioxide (1,4-dithiane sulfone, 5), derived from the enthalpy of combustion in oxygen, measured by a rotating bomb calorimeter and the variation of vapor pressures with temperatures determined by the Knudsen effusion technique. The theoretically estimated enthalpy of formation was calculated from high-level ab initio molecular orbital calculations at the G2(MP2) level. The theoretical calculations appear to be in very good agreement with experiment. A comparison of the conversion of thiane sulfone 3 to 1,3-dithiane sulfone 4 and 1,4-dithiane sulfone 5 clearly shows the 1,3 isomer to be 6.7 kJ mol(-1) less stable, probably owing to diminished electrostatic repulsion between the sulfur heteroatoms in 1,4-sulfone 5. PMID:16555808

  17. Synthesis and characterization of two sulfonated resorcinarenes: a new example of a linear array of sodium centers and macrocycles.

    PubMed

    Sanabria, Edilma; Esteso, Miguel Ángel; Pérez-Redondo, Adrián; Vargas, Edgar; Maldonado, Mauricio

    2015-01-01

    Two sulfonated resorcinarenes were synthesized by reacting C-tetra(butyl) resorcinarene or C-tetra(2-(methylthio)ethyl)resorcinarene with formaldehyde in the presence of sodium sulfite. Their structures were determined via FT-IR, 1H-NMR, 13C-NMR and mass spectrometry. Thermal gravimetric analyses of the derivatives were also carried out and revealed the presence of water molecules in the solid state. The sulfonated product of C-tetra(butyl)resorcinarene was characterized by an X-ray crystal structure determination. The asymmetric unit contains eight molecules of water and two of acetone, and analysis indicated that sulfonated resorcinarene prefers a cone configuration (rccc conformation) in the solid state. In the crystal array, classical hydrogen bond interactions O-H···O and intermolecular contacts were observed. In the crystal packing, a linear array of capsules of sulfonated resorcinarenes was generated for a chain of sodium atoms and sulfonate groups. PMID:26029860

  18. Facile synthesis of 4H-chromene derivatives via base-mediated annulation of ortho-hydroxychalcones and 2-bromoallyl sulfones

    PubMed Central

    Thadkapally, Srinivas; Kunjachan, Athira C

    2016-01-01

    Summary The cesium carbonate-mediated reaction of 2-bromoallyl sulfones and ortho-hydroxychalcones furnished 3-arylsulfonyl-4H-chromene derivatives in 58–67% yield (18 examples). 2-Bromoallyl sulfones functioned as synthetic surrogates for allenyl sulfones in the reaction. PMID:26877804

  19. Sulfonic Acid- and Lithium Sulfonate-Grafted Poly(Vinylidene Fluoride) Electrospun Mats As Ionic Liquid Host for Electrochromic Device and Lithium-Ion Battery.

    PubMed

    Zhou, Rui; Liu, Wanshuang; Leong, Yew Wei; Xu, Jianwei; Lu, Xuehong

    2015-08-01

    Electrospun polymer nanofibrous mats loaded with ionic liquids (ILs) are promising nonvolatile electrolytes with high ionic conductivity. The large cations of ILs are, however, difficult to diffuse into solid electrodes, making them unappealing for application in some electrochemical devices. To address this issue, a new strategy is used to introduce proton conduction into an IL-based electrolyte. Poly(vinylidene fluoride-co-hexafluoropropylene) (P(VDF-HFP)) copolymer is functionalized with sulfonic acid through covalent attachment of taurine. The sulfonic acid-grafted P(VDF-HFP) electrospun mats consist of interconnected nanofibers, leading to remarkable improvement in dimensional stability of the mats. IL-based polymer electrolytes are prepared by immersing the modified mats in 1-butyl-3-methylimidazolium tetrafluoroborate (BMIM(+)BF4(-)). It is found that the SO3(-) groups can have Lewis acid-base interactions with the cations (BMIM(+)) of IL to promote the dissociation of ILs, and provide additional proton conduction, resulting in significantly improved ionic conductivity. Using this novel electrolyte, polyaniline-based electrochromic devices show higher transmittance contrast and faster switching behavior. Furthermore, the sulfonic acid-grafted P(VDF-HFP) electrospun mats can also be lithiated, giving additional lithium ion conduction for the IL-based electrolyte, with which Li/LiCoO2 batteries display enhanced C-rate performance.

  20. Sulfonated graphene oxide as effective catalyst for conversion of 5-(hydroxymethyl)-2-furfural into biofuels.

    PubMed

    Antunes, Margarida M; Russo, Patrícia A; Wiper, Paul V; Veiga, Jacinto M; Pillinger, Martyn; Mafra, Luís; Evtuguin, Dmitry V; Pinna, Nicola; Valente, Anabela A

    2014-03-01

    The acid-catalyzed reaction of 5-(hydroxymethyl)-2-furfural with ethanol is a promising route to produce biofuels or fuel additives within the carbohydrate platform; specifically, this reaction may give 5-ethoxymethylfurfural, 5-(ethoxymethyl)furfural diethylacetal, and/or ethyl levulinate (bioEs). It is shown that sulfonated, partially reduced graphene oxide (S-RGO) exhibits a more superior catalytic performance for the production of bioEs than several other acid catalysts, which include sulfonated carbons and the commercial acid resin Amberlyst-15, which has a much higher sulfonic acid content and stronger acidity. This was attributed to the cooperative effects of the sulfonic acid groups and other types of acid sites (e.g., carboxylic acids), and to the enhanced accessibility to the active sites as a result of the 2D structure. Moreover, the acidic functionalities bonded to the S-RGO surface were more stable under the catalytic reaction conditions than those of the other solids tested, which allowed its efficient reuse.

  1. Effect of some petroleum sulfonate surfactants on the apparent water solubility of organic compounds

    SciTech Connect

    Kile, D.E.; Chiou, C.T. ); Helburn, R.S. )

    1990-02-01

    Water solubility enhancements of 1,1-bis(p-chlorophenyl)-2,2,2-trichloroethane (DDT) and 1,2,3-trichlorobenzene (TCB) by some commercial petroleum sulfonates (Petronate L, Petronate HL, and Pyronate 40) were studied at room temperature. Unlike conventional surfactants, the petroleum sulfonate surfactants are mixtures of sulfonated hydrocarbons and free mineral oils, which form stable emulsions in water and thus behave much like a bulk organic phase in concentrating organic solutes. The extent of solubility enhancement is linearly proportional to the concentration of the petroleum sulfonate-oil (PSO) emulsion, in contrast with the effect of a conventional surfactant in which a sharp inflection occurs in the vicinity of the critical micelle concentration (CMC). The enhancement effect of the PSO surfactant is 1.5-3 orders of magnitude greater than that of ordinary surfactant monomers below the CMC. The partition coefficient of the solute between the emulsified PSO phase and water (K{sub em}) is closely related to the nonpolar content of the PSO surfactant; the normalized K{sub em} values are about the same order of magnitude as the solvent (octanol)-water partition coefficients of the solutes.

  2. Distribution and excretion of perfluorooctane sulfonate (PFOS) in beef cattle (Bos taurus)

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Perfluorooctane sulfonate (PFOS), a perfluoroalkyl surfactant used in many industrial products, is present in industrial wastes and in wastewater treatment plant biosolids. Biosolids are commonly applied to pastures and crops used for animal feed; consequently, PFOS may accumulate in the edible tis...

  3. Hierarchical porous carbon derived from sulfonated pitch for electrical double layer capacitors

    NASA Astrophysics Data System (ADS)

    Guo, Yan; Shi, Zhi-qiang; Chen, Ming-ming; Wang, Cheng-yang

    2014-04-01

    Hierarchical porous carbon (HPC) has been synthesized using sulfonated pitch as a precursor with a simple KOH activation process. Sulfonated pitch has a high content of oxygen-containing groups which enable it to be easily wetted in KOH solution and facilitate the activation process. The effect of the activation agent to precursor ratio on the porosity and the specific surface area is studied by nitrogen adsorption-desorption. A maximum specific surface area of 3548 m2 g-1 is achieved with a KOH to sulfonated pitch ratio of 3 and this produces a structure with micro-, meso- and macropores. Among the various HPC samples, the sample prepared with an activation agent to precursor ratio of 1.5 exhibits the best electrochemical performance as an electrode in an electrical double layer capacitor (EDLC) in 6 M KOH electrolyte. Its gravimetric specific capacitance is 157 F g-1 at a current density of 100 A g-1 and it has a capacitance retention ratio of 98.4% even after 10,000 cycles. The sample also presents outstanding electrochemical performance in 1 M Li2SO4 and 1 M TEA BF4/PC electrolytes. Thus, HPC derived from sulfonated pitch is a promising electrode material for EDLCs.

  4. SWELLING OF PEATS IN LIQUID METHYL, TETRAMETHYLENE AND PROPYL SULFOXIDES AND IN LIQUID PROPYL SULFONE

    EPA Science Inventory

    The interactions of methyl, tetramethylene, and propyl sulfoxides and propyl sulfone during sorption onto four de-waxed, acid-form peats have been studied by means of swelling measurements. The results for sulfoxides are displayed as het-eromolecular sorption isotherms, which plo...

  5. POLYSTYRENE SULFONIC ACID CATALYZED GREENER SYNTHESIS OF HYDRAZONES IN AQUEOUS MEDIUM USING MICROWAVES

    EPA Science Inventory

    An environmentally benign aqueous protocol for the synthesis of cyclic, bi-cyclic, and heterocyclic hydrazones using polystyrene sulfonic acid (PSSA) as a catalyst has been developed; the simple reaction proceeds efficiently in water in the absence of any organic solvent under mi...

  6. Rh-catalyzed sulfonic acid group directed ortho C-H olefination of arenes.

    PubMed

    Dong, Yi; Liu, Gang

    2013-09-21

    A Rh-catalyzed ortho C-H olefination of arenes directed by a sulfonic acid group was developed with good yields and a broad reaction scope. Efficient performance of the catalyst caused this electron-poor aromatic C-H to be activated effectively and unactivated alkenes are also suitable for this reaction.

  7. Adsorption of cadmium ions on thiol or sulfonic-functionalized poly(dimethylsiloxane) networks.

    PubMed

    Silva, Fábio A B; Pissetti, Fábio L

    2014-02-15

    Thiol or sulfonic-functionalized poly(dimethylsiloxane) elastomeric networks were prepared from 3-mercaptopropyltrimethoxysilane or the oxidized silane. The characterization of these materials using infrared spectroscopy (IR) and (13)C/(29)Si nuclear magnetic resonance (NMR) suggested that the materials were functionalized with the aforementioned groups and that the networks are composed of linear segments of PDMS crosslinked by nodes of silsesquioxanes, which contain T(3) and/or T(2) type silicon. The thermogravimetric analysis of the polymeric networks revealed that they exhibit good thermal stability. The adsorption capacities for cadmium ions in ethanolic solutions were 0.33 and 0.89 mmol g(-1) for the thiol- and sulfonic-functionalized PDMS networks, respectively. In water solution the material with thiol group do not adsorbed Cd (II), however, the network with sulfonic group adsorbed 0.70 mmol g(-1). In ethanol, the linearization of the adsorption isotherms revealed that the Langmuir model describes the interaction between the adsorbate-adsorbent, in water, the Freundlich adsorption model described the metal adsorption for the sulfonic-functionalized PDMS.

  8. Effective and selective bisphenol A synthesis on a layered silicate with spatially arranged sulfonic acid.

    PubMed

    Ide, Yusuke; Kagawa, Noriko; Itakura, Masaya; Imae, Ichiro; Sadakane, Masahiro; Sano, Tsuneji

    2012-04-01

    The silylated derivatives of a layered alkali silicate, magadiite, modified with propylsulfonic or arylsulfonic acid were synthesized and used as catalysts for an acid-catalyzed condensation of phenol with acetone. The propylsulfonated magadiites with a different amount of the attached silyl group were synthesized by the silylation of the dodecylammonium-exchanged magadiite with the tuned amount of 3-(mercaptopropyl)trimethoxysilane and the subsequent oxidation of the attached thiol to sulfonic acid. The arylsulfonated magadiite was synthesized by the silylation of the dodecylammonium-exchanged magadiite with 2-(4-chlorosulfonylphenyl)ethyltrimethoxysilane and the subsequent hydrolysis of the attached sulfonyl chloride to sulfonic acid. The X-ray diffraction (XRD) patterns and elemental mappings of the products, and the photoluminescent spectra of the Eu(3+)-exchanged products suggested that propylsulfonic or arylsulfonic acid was homogeneously distributed in the interlayer space. When all the sulfonated materials were used as an acid catalyst for condensation between phenol and acetone, p,p' bisphenol A selectively formed over the o,p' isomer, and higher yield and selectivity were attained on the catalysts with larger amount of the attached sulfonic acid. When the interlayer space of the propylsulfonated magadiite was expanded by the co-attachment of octadecylsilyl group, lower selectivity was obtained. The arylsulfonated magadiite showed considerably higher p,p' bisphenol A yield than the propylsulfonated magadiites.

  9. Wine metabolomics reveals new sulfonated products in bottled white wines, promoted by small amounts of oxygen.

    PubMed

    Arapitsas, Panagiotis; Ugliano, Maurizio; Perenzoni, Daniele; Angeli, Andrea; Pangrazzi, Paolo; Mattivi, Fulvio

    2016-01-15

    The impact of minute amounts of oxygen in the headspace on the post-bottling development of wine is generally considered to be very important, since oxygen can either damage or improve the quality of wine. This project aimed to gain new experimental evidence about the chemistry of the interaction between wine and oxygen. The experimental design included 216 bottles of 12 different white wines produced from 6 different cultivars (Inzolia, Muller Thurgau, Chardonnay, Grillo, Traminer and Pinot gris). Half of them were bottled using the standard industrial process with inert headspace and the other half without inert gas and with extra headspace. After 60 days of storage at room temperature, the wines were analysed using an untargeted LC-MS method. The use of a detailed holistic analysis workflow, with several levels of quality control and marker selection, gave 35 metabolites putatively induced by the different amounts of oxygen. These metabolite markers included ascorbic acid, tartaric acid and various sulfonated compounds observed in wine for the first time (e.g. S-sulfonated cysteine, glutathione and pantetheine; and sulfonated indole-3-lactic acid hexoside and tryptophol). The consumption of SO2 mediated by these sulfonation reactions was promoted by the presence of higher levels of oxygen on bottling. PMID:26709023

  10. Crystal structure of sodium (1S)-d-lyxit-1-yl-sulfonate.

    PubMed

    Haines, Alan H; Hughes, David L

    2016-05-01

    The title compound, Na(+)·C5H11O8S(-) [systematic name: sodium (1S,2S,3S,4R)-1,2,3,4,5-penta-hydroxy-pentane-1-sulfonate], is formed by reaction of d-lyxose with sodium bis-ulfite (sodium hydrogen sulfite) in water. The anion has an open-chain structure in which one of the oxygen atoms of the sulfonate residue, the S atom, the C atoms of the sugar chain and the O atom of the hy-droxy-methyl group form an essentially planar zigzag chain with the corresponding torsion angles lying between 179.80 (11) and 167.74 (14)°. A three-dimensional bonding network exists in the crystal structure involving hexa-coordination of sodium ions by O atoms, three of which are provided by a single d-lyxose-sulfonate unit and the other three by two sulfonate groups and one hy-droxy-methyl group, each from separate units of the adduct. Extensive inter-molecular O-H⋯O hydrogen bonding supplements this bonding network. PMID:27308005

  11. EFFECTS OF PERFLUOROOCTANE SULFONATE (PFOS) ON MATERNAL AND DEVELOPMENTAL THYROID STATUS IN THE RAT

    EPA Science Inventory

    EFFECTS OF PERFLUOROOCTANE SULFONATE (PFOS) ON MATERNAL AND DEVELOPMENTAL THYROID STATUS IN THE RAT. JR Thibodeaux1, R Hanson1, B Grey1, JM Rogers1, ME Stanton2, and C Lau1. 1Reproductive Toxicology Division; 2Neurotoxicology Division, NHEERL, ORD, US EPA, Research Triangle P...

  12. Pharmacokinetic profiles of perfluorobutane sulfonate and activation of hepatic genes in mice

    EPA Science Inventory

    Polyfluoroalkyl substances (PFAS) are organic chemicals with wide industrial and consumer uses. They are found ubiquitously at low levels in the environment and detectable in humans and wildlife. Perfluorobutane Sulfonate (PFBS) is a short-chained PFAS used to replace perfluorooc...

  13. Perfluoroctane sulfonate-induced changes in fetal rat liver gene expression

    EPA Science Inventory

    In utero exposure of rats to perfluorooctane sulfonate (PFOS, C8F17SO3), a widely disseminated product of the surfactant and coating industries, is associated with residual hepatoxic complications in the surviving offspring. This hepatocellular hypertrophy resembles that observe...

  14. Synthesis of sulfonated porous carbon nanospheres solid acid by a facile chemical activation route

    NASA Astrophysics Data System (ADS)

    Chang, Binbin; Guo, Yanzhen; Yin, Hang; Zhang, Shouren; Yang, Baocheng

    2015-01-01

    Generally, porous carbon nanospheres materials are usually prepared via a template method, which is a multi-steps and high-cost strategy. Here, we reported a porous carbon nanosphere solid acid with high surface area and superior porosity, as well as uniform nanospheical morphology, which prepared by a facile chemical activation with ZnCl2 using resorcinol-formaldehyde (RF) resins spheres as precursor. The activation of RF resins spheres by ZnCl2 at 400 °C brought high surface area and large volume, and simultaneously retained numerous oxygen-containing and hydrogen-containing groups due to the relatively low processing temperature. The presence of these functional groups is favorable for the modification of -SO3H groups by a followed sulfonation treating with sulphuric acid and organic sulfonic acid. The results of N2 adsorption-desorption and electron microscopy clearly showed the preservation of porous structure and nanospherical morphology. Infrared spectra certified the variation of surface functional groups after activation and the successful modification of -SO3H groups after sulfonation. The acidities of catalysts were estimated by an indirect titration method and the modified amount of -SO3H groups were examined by energy dispersive spectra. The results suggested sulfonated porous carbon nanospheres catalysts possessed high acidities and -SO3H densities, which endowed their significantly catalytic activities for biodiesel production. Furthermore, their excellent stability and recycling property were also demonstrated by five consecutive cycles.

  15. Sulfonated mesoporous silica-carbon composites and their use as solid acid catalysts

    NASA Astrophysics Data System (ADS)

    Valle-Vigón, Patricia; Sevilla, Marta; Fuertes, Antonio B.

    2012-11-01

    The synthesis of highly functionalized porous silica-carbon composites made up of sulfonic groups attached to a carbon layer coating the pores of three types of mesostructured silica (i.e. SBA-15, KIT-6 and mesocellular silica) is presented. The synthesis procedure involves the following steps: (a) removal of the surfactant, (b) impregnation of the silica pores with a carbon precursor, (c) carbonization and (d) sulfonation. The resulting silica-carbon composites contain ˜30 wt % of carbonaceous matter with a high density of acidic groups attached to the deposited carbon (i.e.sbnd SO3H, sbnd COOH and sbnd OH). The structural characteristics of the parent silica are retained in the composite materials, which exhibit a high surface area, a large pore volume and a well-ordered porosity made up uniform mesopores. The high density of the sulfonic groups in combination with the mesoporous structure of the composites ensures that a large number of active sites are easily accessible to reactants. These sulfonated silica-carbon composites behave as eco-friendly, active, selective, water tolerant and recyclable solid acids. In this study we demonstrate the usefulness of these composites as solid acid catalysts for the esterification of maleic anhydride, succinic acid and oleic acid with ethanol. These composites exhibit a superior intrinsic catalytic activity to other commercial solid acids such as Amberlyst-15.

  16. GENE PROFILING IN WILD-TYPE AND PPARα-NULL MICE EXPOSED TO PERFLUOROOCTANE SULFONATE

    EPA Science Inventory

    Perfluorooctane sulfonate (PFOS), a perfluoroalkyl acid (PFAA), is a persistent environmental contaminant found in the tissues of humans and wildlife. Over the last decade, health concerns have been raised, in part, because of the long half-life of PFOS and other PFAAs in humans,...

  17. Synthesis and characterization of silica-based hyper-crosslinked sulfonate-modified reversed stationary phases

    PubMed Central

    Luo, Hao; Ma, Lianjia; Zhang, Yu; Carr, Peter W.

    2011-01-01

    A novel type of silica-based sulfonate-modified reversed phase (−SO3-HC-C8 ) has been synthesized; it is based on a newly developed acid stable “hyper-crosslinked” C8 derivatized reversed phase, denoted HC-C8. The −SO3-HC-C8 phases containing controlled amounts of sulfonyl groups were made by sulfonating the aromatic hyper-crosslinked network of the HC-C8 phase at different temperatures. The −SO3-HC-C8 phases are only slightly less hydrophobic than the parent HC-C8 phase. The added sulfonyl groups provide a unique strong cation-exchange selectivity to the hydrophobic hyper-crosslinked substrate as indicated by the very large C coefficient as shown by Snyder’s hydrophobic subtraction reversed-phase characterization method. This cation-exchange activity clearly distinguishes the sulfonated phase from all other reversed phases as confirmed by the extraordinary high values of Snyder’s column comparison function Fs. In addition, as was found in previous studies of silica-based and zirconia-based reversed phases, a strong correlation between the cation-exchange interaction and hydrophobic interaction was observed for these sulfonated phases in studies of the retention of cationic solutes. The overall chromatographic selectivity of these −SO3-HC-C8 phases is greatly enhanced by its high hydrophobicity through a “hydrophobically assisted” ion-exchange retention process. PMID:18207150

  18. 40 CFR 721.9597 - Salt of a substituted sulfonated aryl azo compound (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... azo compound (generic). 721.9597 Section 721.9597 Protection of Environment ENVIRONMENTAL PROTECTION... compound (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as salt of a substituted sulfonated aryl azo compound (PMN P-00-0094)...

  19. 40 CFR 721.9597 - Salt of a substituted sulfonated aryl azo compound (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... azo compound (generic). 721.9597 Section 721.9597 Protection of Environment ENVIRONMENTAL PROTECTION... compound (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as salt of a substituted sulfonated aryl azo compound (PMN P-00-0094)...

  20. 40 CFR 721.9597 - Salt of a substituted sulfonated aryl azo compound (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... azo compound (generic). 721.9597 Section 721.9597 Protection of Environment ENVIRONMENTAL PROTECTION... compound (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as salt of a substituted sulfonated aryl azo compound (PMN P-00-0094)...