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Sample records for aktivatsiya svyazi c-s

  1. Microbial cleavage of organic C-S bonds

    DOEpatents

    Kilbane, II, John J.

    1994-01-01

    A microbial process for selective cleavage of organic C--S bonds which may be used for reducing the sulfur content of sulfur-containing organic carbonaceous materials, Microorganisms of Rhodococcus rhodochrous and Bacillus sphaericus have been found which have the ability of selective cleavage of organic C--S bonds. Particularly preferred microorganisms are Rhodococcus rhodochrous strain ATCC 53968 and Bacillus sphaericus strain ATCC 53969 and their derivatives.

  2. Microbial cleavage of organic C-S bonds

    DOEpatents

    Kilbane, J.J. II.

    1994-10-25

    A microbial process is described for selective cleavage of organic C-S bonds which may be used for reducing the sulfur content of sulfur-containing organic carbonaceous materials. Microorganisms of Rhodococcus rhodochrous and Bacillus sphaericus have been found which have the ability of selective cleavage of organic C-S bonds. Particularly preferred microorganisms are Rhodococcus rhodochrous strain ATCC 53968 and Bacillus sphaericus strain ATCC 53969 and their derivatives.

  3. Bond activation with an apparently benign ethynyl dithiocarbamate Ar-C≡C-S-C(S)NR2.

    PubMed

    Ung, Gaël; Frey, Guido D; Schoeller, Wolfgang W; Bertrand, Guy

    2011-10-10

    The hedgehog molecule: A simple ethynyl dithiocarbamate [Ar-C≡C-S-C(S)NR(2)] is able to cleave a broad range of enthalpically strong σ bonds and to activate carbon dioxide and elemental sulfur. Depending on the substrate, the bond activation process involves either the existence of an equilibrium with the nonobservable mesoionic carbene isomer or the cooperation of the nucleophilic carbon-carbon triple bond and the electrophilic CS carbon atom. PMID:23210141

  4. C. S. Peirce's Dialogical Conception of Sign Processes

    ERIC Educational Resources Information Center

    Bergman, Mats

    2005-01-01

    This article examines the contention that the central concepts of C. S. Peirce's semeiotic are inherently communicational. It is argued that the Peircean approach avoids the pitfalls of objectivism and constructivism, rendering the sign-user neither a passive recipient nor an omnipotent creator of meaning. Consequently, semeiotic may serve as a…

  5. The Use of C. S. Lewis's "Poems" for Oral Interpretation.

    ERIC Educational Resources Information Center

    Keefe, Carolyn

    Suggestions are offered in this paper for adapting C. S. Lewis's poems for oral interpretation. A discussion of Lewis's lifelong correspondence with his friend Arthur Greeves provides insights into Lewis's perceptions of his own writing. Eighty poems selected from Lewis's "Poems" as appropriate for oral interpretation are classified according to…

  6. C-S bond cleavage by a polyketide synthase domain

    PubMed Central

    Ma, Ming; Lohman, Jeremy R.; Liu, Tao; Shen, Ben

    2015-01-01

    Leinamycin (LNM) is a sulfur-containing antitumor antibiotic featuring an unusual 1,3-dioxo-1,2-dithiolane moiety that is spiro-fused to a thiazole-containing 18-membered lactam ring. The 1,3-dioxo-1,2-dithiolane moiety is essential for LNM’s antitumor activity, by virtue of its ability to generate an episulfonium ion intermediate capable of alkylating DNA. We have previously cloned and sequenced the lnm gene cluster from Streptomyces atroolivaceus S-140. In vivo and in vitro characterizations of the LNM biosynthetic machinery have since established that: (i) the 18-membered macrolactam backbone is synthesized by LnmP, LnmQ, LnmJ, LnmI, and LnmG, (ii) the alkyl branch at C-3 of LNM is installed by LnmK, LnmL, LnmM, and LnmF, and (iii) leinamycin E1 (LNM E1), bearing a thiol moiety at C-3, is the nascent product of the LNM hybrid nonribosomal peptide synthetase (NRPS)-acyltransferase (AT)-less type I polyketide synthase (PKS). Sulfur incorporation at C-3 of LNM E1, however, has not been addressed. Here we report that: (i) the bioinformatics analysis reveals a pyridoxal phosphate (PLP)-dependent domain, we termed cysteine lyase (SH) domain (LnmJ-SH), within PKS module-8 of LnmJ; (ii) the LnmJ-SH domain catalyzes C-S bond cleavage by using l-cysteine and l-cysteine S-modified analogs as substrates through a PLP-dependent β-elimination reaction, establishing l-cysteine as the origin of sulfur at C-3 of LNM; and (iii) the LnmJ-SH domain, sharing no sequence homology with any other enzymes catalyzing C-S bond cleavage, represents a new family of PKS domains that expands the chemistry and enzymology of PKSs and might be exploited to incorporate sulfur into polyketide natural products by PKS engineering. PMID:26240335

  7. Surface carbonation of synthetic C-S-H samples: A comparison between fresh and aged C-S-H using X-ray photoelectron spectroscopy

    SciTech Connect

    Black, Leon Garbev, Krassimir; Gee, Ian

    2008-06-15

    This paper presents a continuation of studies into silicate anion structure using X-ray photoelectron spectroscopy (XPS). A series of C-S-H samples have been prepared mechanochemically, and then stored under ambient conditions for six months. Storage led to surface carbonation, the extent of which was dependent upon the calcium/silicon ratio of the fresh sample. Carbonation arose through decalcification of the C-S-H, leading to increased silicate polymerisation. The surfaces of the most calcium-rich phases (C/S = 1.33 and 1.50) underwent complete decalcification to yield silica (possibly containing some silanol groups) and calcium carbonate. Carbonation, and hence changes in silicate anion structure, was minimal for the C-S-H phases with C/S = 0.67 and 0.75.

  8. Spectroscopy study of Zn, Cd, Pb and Cr ions immobilization on C-S-H phase

    NASA Astrophysics Data System (ADS)

    Żak, Renata; Deja, Jan

    2015-01-01

    Calcium silicate hydrates (C-S-H) have a large number of structural sites available for cations and anions to bind. The C-S-H phases are materials which have ability to toxic ions immobilization. Immobilization mechanisms for C-S-H include sorption, phase mixing, substitution and precipitation of insoluble compounds. This study presents the C-S-H (prepared with C/S ratios 1.0) phase as absorbent for immobilization of Zn, Cd, Pb and Cr ions. The C-S-H spectra before and after incorporation of heavy metals ions into the C-S-H structure were obtained. The effect of added heavy metals ions on the hydration phenomena was studied by means of X-ray diffractions analysis. FTIR spectra was measured. The microstructure and phase composition of C-S-H indicate that they can play an essential role in the immobilization of heavy metals. The properties of C-S-H in the presence of Zn, Cd, Pb and Cr cations were studied. The leaching ML test was used to evaluate the level of immobilization of heavy metals in C-S-H. The leached solutions are diluted and analyzed using atomic absorption spectrometry (AAS) and the activated solid particles are separated, washed, desiccated and analyzed by Fourier transform infrared (FTIR) spectroscopy. It was found that the degree of Cd, Zn, Pb and Cr cations immobilization was very high (exceeding 99.96%).

  9. Spectroscopy study of Zn, Cd, Pb and Cr ions immobilization on C-S-H phase.

    PubMed

    Żak, Renata; Deja, Jan

    2015-01-01

    Calcium silicate hydrates (C-S-H) have a large number of structural sites available for cations and anions to bind. The C-S-H phases are materials which have ability to toxic ions immobilization. Immobilization mechanisms for C-S-H include sorption, phase mixing, substitution and precipitation of insoluble compounds. This study presents the C-S-H (prepared with C/S ratios 1.0) phase as absorbent for immobilization of Zn, Cd, Pb and Cr ions. The C-S-H spectra before and after incorporation of heavy metals ions into the C-S-H structure were obtained. The effect of added heavy metals ions on the hydration phenomena was studied by means of X-ray diffractions analysis. FTIR spectra was measured. The microstructure and phase composition of C-S-H indicate that they can play an essential role in the immobilization of heavy metals. The properties of C-S-H in the presence of Zn, Cd, Pb and Cr cations were studied. The leaching ML test was used to evaluate the level of immobilization of heavy metals in C-S-H. The leached solutions are diluted and analyzed using atomic absorption spectrometry (AAS) and the activated solid particles are separated, washed, desiccated and analyzed by Fourier transform infrared (FTIR) spectroscopy. It was found that the degree of Cd, Zn, Pb and Cr cations immobilization was very high (exceeding 99.96%). PMID:25106815

  10. Effect of temperature on the microstructure of calcium silicate hydrate (C-S-H)

    SciTech Connect

    Gallucci, E. Zhang, X.; Scrivener, K.L.

    2013-11-15

    Temperature affects the properties of concrete through its effect on the hydration of cement and its associated microstructural development. This paper focuses on the modifications to C-S-H induced by isothermal curing between 5 and 60 °C. The results show that as the temperature increases (within the range studied) the C/S ratio of C-S-H changes only slightly, with a higher degree of polymerisation of silicate chains, but there is a significant decrease in its bound water content and an increase of apparent density of 25%. This increase seems to come from a different packing of C-S-H at the nanoscale. As a consequence of these changes, the microstructure of the cement paste is much coarser and porous, which explains the lower final strengths obtained by curing at elevated temperatures. -- Highlights: •C-S-H structure studied at the atomic level •Multiple analytical techniques used •Studies conducted at temperatures above and below normal temperatures.

  11. Changes in the elastic moduli of C-S-H due to presence of interlaminar cations

    NASA Astrophysics Data System (ADS)

    Mejia, Shirley; Hoyos, Bibian

    2016-03-01

    A set of models of calcium silicate hydrate (C-S-H) with alkali cations in the interlaminar layer, various calcium/silicon ratios, and each with a density of 2.4 g cm-3 is presented. Using molecular simulation techniques, the objective was to study how the Young’s, bulk, and shear modulus, as well as the Poisson’s ratio changed due to the presence of monovalent ions. The effect of density on the elastic moduli was neglected, thus the NVT ensemble was used. Comparing the different simulation cells, it was found that models with sodium and potassium ions in the structure and an alkali/silicon ratio of 0.18 showed negative effects on the elastic moduli of C-S-H. This could be mainly ascribed to the shielding effect of the alkali on the interlaminar interactions that contribute to the cohesion between the layers of C-S-H.

  12. Incorporation of zinc into calcium silicate hydrates, Part I: formation of C-S-H(I) with C/S=2/3 and its isochemical counterpart gyrolite

    SciTech Connect

    Stumm, Andreas . E-mail: andreas.stumm@itc-wgt.fzk.de; Garbev, Krassimir; Beuchle, Guenter; Black, Leon; Stemmermann, Peter; Nueesch, Rolf

    2005-09-01

    We have investigated the incorporation of zinc into both nanocrystalline and crystalline calcium silicate hydrates with starting C/S ratios of 2/3 (0.66). Zinc was added replacing calcium in the starting mixtures [Zn/(Zn+Ca)=0-1/4; 0-10 wt.% Zn], and the resultant phases were characterised using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), differential thermal analysis-thermogravimetry (DTA-TG) and environmental scanning electron microscopy (ESEM). In both groups of samples, increasing zinc content led to gradual structural changes, until eventually a second phase was formed. Zinc was incorporated to similar limits in both sets of samples. The thermal stability of the structures increased to a certain zinc content, beyond which there was structural destabilisation. Zinc incorporation is possible up to {approx}6 wt.%. Our observations strongly indicate similar zinc incorporation mechanisms in both sample series, namely incorporation of zinc into the interlayer of C-S-H(I) and the X-sheet of gyrolite for nanocrystalline and crystalline samples, respectively.

  13. P.H.Y.S.I.C.S. Can Be Done!

    ERIC Educational Resources Information Center

    Spangler, Lois

    2004-01-01

    P.H.Y.S.I.C.S. (Physics Headstart Yearlong Science Inquiry at Central School) is a series of inquiry investigations and science activities designed to motivate students and teachers and develop a love of physics in our rural agricultural community. The program?s approach infuses physics into the science curriculum while capitalizing on our…

  14. 363. A.C.S., Delineator March 1934 STATE OF CALIFORNIA; DEPARTMENT OF ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    363. A.C.S., Delineator March 1934 STATE OF CALIFORNIA; DEPARTMENT OF PUBLIC WORKS; SAN FRANCISCO - OAKLAND BAY BRIDGE; CONTRACT NO. 6A; SUPERSTRUCTURE - WEST BAY CROSSING; SAN FRANCISCO ANCHORAGE; AMERICAN BRIDGE CO.; AMBRIDGE PLANT; ORDER NO. G4866; SHEET NO E3 - San Francisco Oakland Bay Bridge, Spanning San Francisco Bay, San Francisco, San Francisco County, CA

  15. 378. A.C.S., Delineator March 1933 STATE OF CALIFORNIA; DEPARTMENT OF ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    378. A.C.S., Delineator March 1933 STATE OF CALIFORNIA; DEPARTMENT OF PUBLIC WORKS; SAN FRANCISCO - OAKLAND BAY BRIDGE; CONTRACT NO. 6A; SUPERSTRUCTURE - WEST BAY CROSSING; YERBA BUENA ANCHORAGE & CABLE BENT. AMERICAN BRIDGE CO.; AMBRIDGE PLANT; ORDER NO. G 4866; SHEET NO. E4 - San Francisco Oakland Bay Bridge, Spanning San Francisco Bay, San Francisco, San Francisco County, CA

  16. An Integrated Perspective of Humanism and Supernaturalism for Education: C. S. Lewis's Version of Education

    ERIC Educational Resources Information Center

    Lee, Seung Chun

    2013-01-01

    This paper explores some theoretical reflections on the connection between C. S. Lewis's thoughts on the purpose and process of education and his understanding of supernatural human nature which has been relatively little explored. An introduction about Lewis's career as a college teacher blends into the background of this paper. It is followed by…

  17. Rhodium-Catalyzed ipso-Borylation of Alkylthioarenes via C-S Bond Cleavage.

    PubMed

    Uetake, Yuta; Niwa, Takashi; Hosoya, Takamitsu

    2016-06-01

    Rhodium-catalyzed transformation of alkyl aryl sulfides into arylboronic acid pinacol esters via C-S bond cleavage is reported. In combination with transition-metal-catalyzed sulfanyl group-guided regioselective C-H borylation reactions of alkylthioarenes, this method allows the synthesis of a diverse range of multisubstituted arenes. PMID:27210907

  18. Mathematics, Art, Research, Collaboration, and Storytelling: The High M.A.R.C.S. Project

    ERIC Educational Resources Information Center

    Reilly, Edel M.; Pagnucci, Gian S.

    2007-01-01

    This article describes a curriculum integration project designed to help students better contextualize their learning: The High M.A.R.C.S. Project linked mathematics, art, research, collaboration, and storytelling. The article explains the project in detail, discusses sample student work from the project, and describes how the project work was…

  19. Paradise Lost and Found: Obedience, Disobedience, and Storytelling in C.S. Lewis and Philip Pullman.

    ERIC Educational Resources Information Center

    Wood, Naomi

    2001-01-01

    Considers how in the fantasy series "The Chronicles of Narnia" and "His Dark Materials," by C.S. Lewis and Philip Pullman respectively, the authors use symbols and themes from "Paradise Lost." Notes that each author's narrative choice uses his view of cosmic order to persuade readers that obedience should be understood as central to coming of age.…

  20. Oral Interpretation of C.S. Lewis'"Narnia Tales": A Refracting of "Pictures."

    ERIC Educational Resources Information Center

    Keefe, Carolyn

    "The Chronicles of Narnia" are a series of seven fairy tales written by C.S. Lewis that have become popular with both children and adults. Lewis points to five aspects of the fairy tale form that made the form suitable for expressing the images he saw. The aspects are: (1) no love interest; (2) no close psychology; (3) severe restraints on…

  1. Dorothy L. Sayers and C. S. Lewis: Christian Postmodernism beyond Boundaries

    ERIC Educational Resources Information Center

    Yuasa, Kyoko

    2012-01-01

    Modern critics do not consider science fiction and mystery novels to be "serious reading", but Dorothy L. Sayers and C. S. Lewis questioned the boundaries between "popular" and "serious" literature. Both Christian writers critically discuss the spiritual crisis of the modern world in each fiction genre. This paper will discuss Sayers and Lewis…

  2. Sulfide synthesis through copper-catalyzed C-S bond formation under biomolecule-compatible conditions.

    PubMed

    Zhang, Yonghong; Li, Yiming; Zhang, Xiaomei; Jiang, Xuefeng

    2015-01-18

    We report here an efficient and mild method for constructing C-S bonds. The reactions were carried out with Na2S2O3 as a sulfurating reagent, CuSO4 as a catalyst, and water as solvent without any surfactant. The products were achieved in moderate to excellent yields at room temperature under air. Notably, this reaction is compatible with various biomolecules including amino acids, oligosaccharides, nucleosides, proteins, and cell lysates. PMID:25435202

  3. Ruthenium Catalyzed Intramolecular C-S Coupling Reactions: Synthetic Scope and Mechanistic Insight.

    PubMed

    Sharma, Shivani; Pathare, Ramdas S; Maurya, Antim K; Gopal, Kandasamy; Roy, Tapta Kanchan; Sawant, Devesh M; Pardasani, Ram T

    2016-02-01

    A ruthenium catalyzed intramolecular C-S coupling reaction of N-arylthioureas for the synthesis of 2-aminobenzothiazoles has been developed. Kinetic, isotope labeling, and computational studies reveal the involvement of an electrophilic ruthenation pathway instead of a direct C-H activation. Stereoelectronic effect of meta-substituents on the N-arylthiourea dictates the final regioselective outcome of the reaction. PMID:26761401

  4. The selectionist meaning of C. S. Peirce and B. F. Skinner.

    PubMed

    Moxley, Roy A

    2002-01-01

    The selectionist meaning of C. S. Peirce and B. F. Skinner, which has an empirical existence, is advanced against essentialist meaning, which does not. Against a tradition that advocates essentialist meanings, the development of selectionist meaning is traced from Darwin through Peirce and on to Skinner. The views of Peirce and Skinner on meaning are presented as sharing a compatible conceptual foundation with contrasting but complementary distinctions. Support for selectionist meaning comes from contemporary dictionary construction, pragmatist philosophers, and recent views of scientific verbal behavior. Some implications are discussed. PMID:22477230

  5. The selectionist meaning of C. S. Peirce and B. F. Skinner

    PubMed Central

    Moxley, Roy A.

    2002-01-01

    The selectionist meaning of C. S. Peirce and B. F. Skinner, which has an empirical existence, is advanced against essentialist meaning, which does not. Against a tradition that advocates essentialist meanings, the development of selectionist meaning is traced from Darwin through Peirce and on to Skinner. The views of Peirce and Skinner on meaning are presented as sharing a compatible conceptual foundation with contrasting but complementary distinctions. Support for selectionist meaning comes from contemporary dictionary construction, pragmatist philosophers, and recent views of scientific verbal behavior. Some implications are discussed. PMID:22477230

  6. Manganese-catalyzed regiospecific sp(3) C-S bond formation through C-C bond cleavage of cyclobutanols.

    PubMed

    Ren, Rongguo; Wu, Zhen; Zhu, Chen

    2016-06-21

    A manganese-catalyzed regioselective sp(3) C-S bond formation through C-C bond cleavage of cyclobutanols is described. A variety of primary and secondary alkyl thioethers are efficiently prepared under mild reaction conditions. The mechanistic pathways involving radical-mediated tandem C-C bond cleavage and C-S bond formation are proposed. PMID:27279018

  7. ASM Triggered too Observations of 100,000 C/s Black-Hole Candidates

    NASA Astrophysics Data System (ADS)

    van der Klis, Michiel

    Resubmission accepted Cycle 2-10 proposal. The PCA is unique by the high count rates (~100.000 c/s) it can record, and its resulting extreme sensitivity to weak variability. Only few sources get this bright. Our RXTE work on Sco X-1 and 1744-28 shows that high count rate observations are very rewarding, but also difficult and not without risk. In the life of the satellite probably only one black hole transient (if any) will reach 10^5 cps/5 PCU levels. When this occurs a window of discovery will be opened on black holes, which will nearly certainly close again within a few days. This proposal aims at ensuring that optimal use is made of this opportunity by performing state of the art high count rate observations covering all of the most crusial aspects of the source variability.

  8. ASM Triggered too Observations of 100,000 C/s Black-Hole Candidates

    NASA Astrophysics Data System (ADS)

    van der Klis, Michiel

    Resubmission accepted Cycle 2-11 proposal. The PCA is unique by the high count rates (~100.000 c/s) it can record, and its resulting extreme sensitivity to weak variability. Only few sources get this bright. Our RXTE work on Sco X-1 and 1744-28 shows that high count rate observations are very rewarding, but also difficult and not without risk. In the life of the satellite probably only one black hole transient (if any) will reach 10^5 cps/5 PCU levels. When this occurs a window of discovery will be opened on black holes, which will nearly certainly close again within a few days. This proposal aims at ensuring that optimal use is made of this opportunity by performing state of the art high count rate observations covering all of the most crusial aspects of the source variability.

  9. Effet de la poudre de verre sur le fluage du C-S-H

    NASA Astrophysics Data System (ADS)

    Danilova, Maryna

    Glass is a unique inert material that could be recycled many times without changing its physical and chemical properties. Nevertheless, for some reason, large quantities of glass are still not recycled and therefore are stored as a waste. Its alternative recycling has become, since long, a major environmental problem. Moreover, glass is a potentially useful material for the development of ecological concrete, consequently, this way valorization seems to be imminent. In this research, characterization of the creep of concrete incorporating waste glass in powder form, i.e. glass powder (GP) as a supplementary cementitious material (GP-concrete) was carried out at a macro- and nanolevels. First, results from experimental study on the under load behaviour of GP-concrete are presented. Different types of strain occurring under load or after unload were discussed: quasi-instantaneous deformation, total mechanical deformation due to the maintained uniaxial compressive load during 1 year, total creep, basic creep, elastic recovery and total recovery. Shrinkage under drying conditions and endogenous shrinkage were also studied. After 1 year creep, the effects of constant load and drying on residual strength were also examined. A comparison was made concerning the final state of the porosity. Afterwards, the thesis reveals the results of tests conducted on the cement paste, going down to its composition and properties of the hydrated phases, in particular of calcium silicate hydrates (C-S-H). All of this, in order to conclude on the harmlessness use of GP regarding to the creep. Keywords : Glass powder, Air-entrained concrete, Creep, Shrinkage, C-S-H, Nanoindentation

  10. Progress report for FACETS (Framework Application for Core-Edge Transport Simulations): C.S. SAP

    SciTech Connect

    Epperly, T W

    2008-10-01

    The mission of the Computer Science Scientific Application Partnership (C.S. SAP) at LLNL is to develop and apply leading-edge scientific component technology to FACETS software. Contributions from LLNL's fusion energy program staff towards the underlying physics modules are described in a separate report. FACETS uses component technology to combine selectively multiple physics and solver software modules written in different languages by different institutions together in an tightly-integrated, parallel computing framework for Tokamak reactor modeling. In the past fiscal year, the C.S. SAP has focused on two primary tasks: applying Babel to connect UEDGE into the FACETS framework through UEDGE's existing Python interface and developing a next generation componentization strategy for UEDGE which avoids the use of Python. The FACETS project uses Babel to solve its language interoperability challenges. Specific accomplishments for the year include: (1) Refined SIDL interfaces for UEDGE to meet satisfy the standard interfaces required by FACETS for all physics modules. This required consensus building between framework and UEDGE developers. (2) Wrote prototype C++ driver for UEDGE to demonstrate how UEDGE can be called from C++ using Babel. (3) Supported the FACETS project by adding new features to Babel such as release number tagging, porting to new machines, and adding new configuration options. Babel modifications were delivered to FACETS by testing and publishing development snapshots in the projects software repository. (4) Assisted Tech-X Corporation in testing and debugging of a high level build system for the complete FACETS tool chain--the complete list of third-party software libraries that FACETS depends on directly or indirectly (e.g., MPI, HDF5, PACT, etc.). (5) Designed and implemented a new approach to wrapping UEDGE as a FACETS component without requiring Python. To get simulation results as soon as possible, our initial connection from the FACETS

  11. The electronic spectrum of the C(s)-C11H3 radical.

    PubMed

    Zhao, Dongfeng; Linnartz, Harold; Ubachs, Wim

    2012-02-01

    The electronic gas-phase absorption spectrum of the bent carbon-chain radical, HC(4)CHC(6)H with C(s) symmetry, is recorded in the 595 nm region by cavity ring-down spectroscopy through an expanding hydrogen plasma. An unambiguous spectroscopic identification becomes possible from a systematic deuterium labeling experiment. A comparison of the results with recently reported spectra of the nonlinear HC(4)CHC(4)H and HC(4)C(C(2)H)C(4)H radicals with C(2v) symmetry provides a more comprehensive understanding of the molecular behavior of π-conjugated bent carbon-chain systems upon electronic excitation. We find that the electronic excitation in the bent carbon-chain HC(4)CHC(2n)H (n = 1-4) series exhibits a similar trend as in the linear HC(2n+1)H (n = 3-6) series, shifting optical absorptions towards longer wavelengths for increasing overall bent chain lengths. The π-conjugation in bent HC(4)CHC(2n)H (n = 1-4) chains is found to be generally smaller than in the linear HC(2n+1)H (n = 3-6) case for equivalent numbers of C-atoms. The addition of an electron-donating group to the bent chain causes a slight decrease of the effective conjugation. PMID:22320742

  12. KIF5C S176 Phosphorylation Regulates Microtubule Binding and Transport Efficiency in Mammalian Neurons

    PubMed Central

    Padzik, Artur; Deshpande, Prasannakumar; Hollos, Patrik; Franker, Mariella; Rannikko, Emmy H.; Cai, Dawen; Prus, Piotr; Mågård, Mats; Westerlund, Nina; Verhey, Kristen J.; James, Peter; Hoogenraad, Casper C.; Coffey, Eleanor T.

    2016-01-01

    Increased phosphorylation of the KIF5 anterograde motor is associated with impaired axonal transport and neurodegeneration, but paradoxically also with normal transport, though the details are not fully defined. JNK phosphorylates KIF5C on S176 in the motor domain; a site that we show is phosphorylated in brain. Microtubule pelleting assays demonstrate that phosphomimetic KIF5C(1-560)S176D associates weakly with microtubules compared to KIF5C(1-560)WT. Consistent with this, 50% of KIF5C(1-560)S176D shows diffuse movement in neurons. However, the remaining 50% remains microtubule bound and displays decreased pausing and increased bidirectional movement. The same directionality switching is observed with KIF5C(1-560)WT in the presence of an active JNK chimera, MKK7-JNK. Yet, in cargo trafficking assays where peroxisome cargo is bound, KIF5C(1-560)S176D-GFP-FRB transports normally to microtubule plus ends. We also find that JNK increases the ATP hydrolysis of KIF5C in vitro. These data suggest that phosphorylation of KIF5C-S176 primes the motor to either disengage entirely from microtubule tracks as previously observed in response to stress, or to display improved efficiency. The final outcome may depend on cargo load and motor ensembles. PMID:27013971

  13. Representations of mind: C. S. Sherrington and scientific opinion, c. 1930-1950.

    PubMed

    Smith, R

    2001-12-01

    Recent writers in the brain sciences and the philosophy of mind contrast modern biological theories of consciousness with a mind-body dualism supposedly dominant half-a-century ago which they regard as scientifically sterile. Reference to C. S. Sherrington often signals the rejected dualism. This paper re-examines Sherrington's highly qualified position and links it to the arguments of British scientists for whom he was a figurehead in the 1930s and 1940s. I interpret the mind-body literature as ancillary to debates about cultural values. From this perspective, dualism represents a defense of a threatened conservative culture. Dismissal of scientists' supposed "dualism" does little to illuminate the tension in their thought between defense of values traditionally associated with mind and hope for an integrated mind-body science. This leads to comments on Sherrington's own concept of integration. The conclusion relates these points to the new research in the brain sciences evident by the end of the 1940s. PMID:12174861

  14. Uptake of Np(IV) by C-S-H phases and cement paste: an EXAFS study.

    PubMed

    Gaona, Xavier; Dähn, Rainer; Tits, Jan; Scheinost, Andreas C; Wieland, Erich

    2011-10-15

    Nuclear waste disposal concepts developed worldwide foresee the use of cementitious materials for the immobilization of long-lived intermediate level waste (ILW). This waste form may contain significant amounts of neptunium-237, which is expected to be present as Np(IV) under the reducing conditions encountered after the closure of the repository. Predicting the release of Np(IV) from the cementitious near field of an ILW repository requires a sufficiently detailed understanding of its interaction with the main sorbing components of hardened cement paste (HCP). In this study, the uptake of Np(IV) by calcium silicate hydrates (C-S-H) and HCP has been investigated using extended X-ray absorption fine structure (EXAFS) spectroscopy. The EXAFS studies on Np(IV)-doped C-S-H and HCP samples reveal that Np(IV) is predominantly incorporated in the structure of C-S-H phases having different Ca:Si ratios. The two main species identified correspond to Np(IV) in C-S-H with a Ca:Si mol ratio of 1.65 as in fresh cement and with a Ca:Si mol ratio of 0.75 as in highly degraded cement. The local structure of Np(IV) changes with the Ca:Si mol ratio and does not depend on pH. Furthermore, Np(IV) shows the same coordination environment in C-S-H and HCP samples. This study shows that C-S-H phases are responsible for the Np(IV) uptake by cementitious materials and further that incorporation in the interlayer of the C-S-H structure is the dominant uptake mechanism. PMID:21879756

  15. High performance C/S composite cathodes with conventional carbonate-based electrolytes in Li-S battery.

    PubMed

    Zheng, Shiyou; Han, Pan; Han, Zhuo; Zhang, Huijuan; Tang, Zhihong; Yang, Junhe

    2014-01-01

    High stable C/S composites are fabricated by a novel high-temperature sulfur infusion into micro-mesoporous carbon method following with solvent cleaning treatment. The C/S composite cathodes show high Coulombic efficiency, long cycling stability and good rate capability in the electrolyte of 1.0 M LiPF6 + EC/DEC (1:1 v/v), for instance, the reversible capacity of the treated C/S-50 (50% S) cathode retains around 860 mAh/g even after 500 cycles and the Coulombic efficiency is close to 100%, which demonstrates the best electrochemical performance of carbon-sulfur composite cathodes using the carbonate-based electrolyte reported to date. It is believed that the chemical bond of C-S is responsible for the superior electrochemical properties in Li-S battery, that is, the strong interaction between S and carbon matrix significantly improves the conductivity of S, effectively buffers the structural strain/stress caused by the large volume change during lithiation/delithiation, completely eliminates the formation of high-order polysulfide intermediates, and substantially avoids the shuttle reaction and the side reaction between polysulfide anions and carbonate solvent, and thus enables the C/S cathode to use conventional carbonate-based electrolytes and achieve outstanding electrochemical properties in Li-S battery. The results may substantially contribute to the progress of the Li-S battery technology. PMID:24776750

  16. High Performance C/S Composite Cathodes with Conventional Carbonate-Based Electrolytes in Li-S Battery

    NASA Astrophysics Data System (ADS)

    Zheng, Shiyou; Han, Pan; Han, Zhuo; Zhang, Huijuan; Tang, Zhihong; Yang, Junhe

    2014-04-01

    High stable C/S composites are fabricated by a novel high-temperature sulfur infusion into micro-mesoporous carbon method following with solvent cleaning treatment. The C/S composite cathodes show high Coulombic efficiency, long cycling stability and good rate capability in the electrolyte of 1.0 M LiPF6 + EC/DEC (1:1 v/v), for instance, the reversible capacity of the treated C/S-50 (50% S) cathode retains around 860 mAh/g even after 500 cycles and the Coulombic efficiency is close to 100%, which demonstrates the best electrochemical performance of carbon-sulfur composite cathodes using the carbonate-based electrolyte reported to date. It is believed that the chemical bond of C-S is responsible for the superior electrochemical properties in Li-S battery, that is, the strong interaction between S and carbon matrix significantly improves the conductivity of S, effectively buffers the structural strain/stress caused by the large volume change during lithiation/delithiation, completely eliminates the formation of high-order polysulfide intermediates, and substantially avoids the shuttle reaction and the side reaction between polysulfide anions and carbonate solvent, and thus enables the C/S cathode to use conventional carbonate-based electrolytes and achieve outstanding electrochemical properties in Li-S battery. The results may substantially contribute to the progress of the Li-S battery technology.

  17. High Performance C/S Composite Cathodes with Conventional Carbonate-Based Electrolytes in Li-S Battery

    PubMed Central

    Zheng, Shiyou; Han, Pan; Han, Zhuo; Zhang, Huijuan; Tang, Zhihong; Yang, Junhe

    2014-01-01

    High stable C/S composites are fabricated by a novel high-temperature sulfur infusion into micro-mesoporous carbon method following with solvent cleaning treatment. The C/S composite cathodes show high Coulombic efficiency, long cycling stability and good rate capability in the electrolyte of 1.0 M LiPF6 + EC/DEC (1:1 v/v), for instance, the reversible capacity of the treated C/S-50 (50% S) cathode retains around 860 mAh/g even after 500 cycles and the Coulombic efficiency is close to 100%, which demonstrates the best electrochemical performance of carbon-sulfur composite cathodes using the carbonate-based electrolyte reported to date. It is believed that the chemical bond of C-S is responsible for the superior electrochemical properties in Li-S battery, that is, the strong interaction between S and carbon matrix significantly improves the conductivity of S, effectively buffers the structural strain/stress caused by the large volume change during lithiation/delithiation, completely eliminates the formation of high-order polysulfide intermediates, and substantially avoids the shuttle reaction and the side reaction between polysulfide anions and carbonate solvent, and thus enables the C/S cathode to use conventional carbonate-based electrolytes and achieve outstanding electrochemical properties in Li-S battery. The results may substantially contribute to the progress of the Li-S battery technology. PMID:24776750

  18. Ransom, Religion, and Red Giants: C.S. Lewis and Fred Hoyle

    NASA Astrophysics Data System (ADS)

    Larsen, Kristine

    2010-01-01

    Famed fantasy writer C.S. Lewis (1898-1963) was known to friends as a well-read astronomy aficionado. However, this medieval scholar and Christian apologist embraced a pre-Copernican universe (with its astrological overtones) in his Chronicles of Narnia series and defended the beauty and relevance of the geocentric model in his final academic work, "The Discarded Image". In the "Ransom Trilogy” ("Out of the Silent Planet", "Perelandra", and "That Hideous Strength") philologist Ransom (loosely based on Lewis's close friend J.R.R. Tolkien) travels to Lewis's visions of Mars and Venus, where he interacts with intelligent extraterrestrials, battles with evil scientists, and aids in the continuation of extraterrestrial Christian values. In the final book, Ransom is joined by a handful of colleagues in open warfare against the satanic N.I.C.E. (National Institute for Coordinated Experiments). Geneticist and evolutionary biologist J.B.S. Haldane criticized Lewis for his scientifically inaccurate descriptions of the planets, and his disdain for the scientific establishment. Lewis responded to the criticism in essays of his own. Another of Lewis's favorite scientific targets was atheist Fred Hoyle, whom he openly criticized for anti-Christian statements in Hoyle's BBC radio series. Writer and Lewis friend Dorothy L. Sayers voiced her own criticism of Hoyle. In a letter, Lewis dismissed Hoyle as "not a great philosopher (and none of my scientific colleagues think much of him as a scientist.” Given Lewis's lack of respect for Hoyle, and use of creative license in describing the planets, and the flat-earth, "geocentric” Narnia, it is surprising that Lewis very carefully includes an astronomically correct description of red giants in two novels in the Narnia series ("The Magician's Nephew" and "The Last Battle"). This inclusion is even more curious given that Fred Hoyle is well-known as one of the pioneers in the field of stellar death and the properties of red giants.

  19. High-resolution Fourier transform synchrotron spectroscopy of the C-S stretching band of methyl mercaptan, CH332SH

    NASA Astrophysics Data System (ADS)

    Lees, R. M.; Xu, Li-Hong; Billinghurst, B. E.

    2016-01-01

    The C-S stretching fundamental band of 12CH332SH, the principal isotopologue of methyl mercaptan, has been investigated by Fourier transform infrared spectroscopy on the Far-Infrared beamline at the Canadian Light Source synchrotron. The band is centered around 710 cm-1 and shows well-resolved a-type parallel structure. Most of the A and E spectral sub-bands have been assigned up to K = 12 for the vt = 0 torsional state and K = 9 for the vt = 1 state, along with a smaller variety of sub-bands for vt = 2. C-S stretching energy term values have been determined employing known ground-state energies, and have been fitted to series expansions in powers of J(J + 1) to determine the substate origins. The origins have in turn been fitted to a Fourier model to characterize the oscillatory torsional energy structure of the C-S stretching state. The amplitude of oscillation of the vt = 0 torsional curves is significantly larger for the C-S stretch state compared to the ground state. A strategy devised to relate this amplitude to an effective torsional barrier height indicates a decrease of about 7% in the effective V3 for the C-S stretch. The vibrational frequency determined for the stretching fundamental from the Fourier fit is 710.3 cm-1. The C-S stretching manifold is crossed by excited vt = 4 torsional levels of the ground state, and strong torsion-vibrational resonant coupling is observed via perturbations in the spectrum together with forbidden sub-bands induced by mixing and intensity borrowing.

  20. Lessons from D.C.'s Evaluation System: Teachers Give IMPACT Low Marks on Support and Professional Development

    ERIC Educational Resources Information Center

    Headden, Susan; Silva, Elena

    2011-01-01

    IMPACT, Washington, D.C.'s controversial evaluation system, sets clear expectations for instruction and holds teachers to well-defined standards of performance. Now into its third year, the program appears to be meeting its goals of rewarding effective teachers and eliminating educators it considers incompetent. And it has given the public reason…

  1. Mechanistic studies of a novel C-S lyase in ergothioneine biosynthesis: the involvement of a sulfenic acid intermediate

    PubMed Central

    Song, Heng; Hu, Wen; Naowarojna, Nathchar; Her, Ampon Sae; Wang, Shu; Desai, Rushil; Qin, Li; Chen, Xiaoping; Liu, Pinghua

    2015-01-01

    Ergothioneine is a histidine thio-derivative isolated in 1909. In ergothioneine biosynthesis, the combination of a mononuclear non-heme iron enzyme catalyzed oxidative C-S bond formation reaction and a PLP-mediated C-S lyase (EgtE) reaction results in a net sulfur transfer from cysteine to histidine side-chain. This demonstrates a new sulfur transfer strategy in the biosynthesis of sulfur-containing natural products. Due to difficulties associated with the overexpression of Mycobacterium smegmatis EgtE protein, the proposed EgtE functionality remained to be verified biochemically. In this study, we have successfully overexpressed and purified M. smegmatis EgtE enzyme and evaluated its activities under different in vitro conditions: C-S lyase reaction using either thioether or sulfoxide as a substrate in the presence or absence of reductants. Results from our biochemical characterizations support the assignment of sulfoxide 4 as the native EgtE substrate and the involvement of a sulfenic acid intermediate in the ergothioneine C-S lyase reaction. PMID:26149121

  2. Mechanistic studies of a novel C-S lyase in ergothioneine biosynthesis: the involvement of a sulfenic acid intermediate.

    PubMed

    Song, Heng; Hu, Wen; Naowarojna, Nathchar; Her, Ampon Sae; Wang, Shu; Desai, Rushil; Qin, Li; Chen, Xiaoping; Liu, Pinghua

    2015-01-01

    Ergothioneine is a histidine thio-derivative isolated in 1909. In ergothioneine biosynthesis, the combination of a mononuclear non-heme iron enzyme catalyzed oxidative C-S bond formation reaction and a PLP-mediated C-S lyase (EgtE) reaction results in a net sulfur transfer from cysteine to histidine side-chain. This demonstrates a new sulfur transfer strategy in the biosynthesis of sulfur-containing natural products. Due to difficulties associated with the overexpression of Mycobacterium smegmatis EgtE protein, the proposed EgtE functionality remained to be verified biochemically. In this study, we have successfully overexpressed and purified M. smegmatis EgtE enzyme and evaluated its activities under different in vitro conditions: C-S lyase reaction using either thioether or sulfoxide as a substrate in the presence or absence of reductants. Results from our biochemical characterizations support the assignment of sulfoxide 4 as the native EgtE substrate and the involvement of a sulfenic acid intermediate in the ergothioneine C-S lyase reaction. PMID:26149121

  3. PONDEROSA-C/S: client-server based software package for automated protein 3D structure determination.

    PubMed

    Lee, Woonghee; Stark, Jaime L; Markley, John L

    2014-11-01

    Peak-picking Of Noe Data Enabled by Restriction Of Shift Assignments-Client Server (PONDEROSA-C/S) builds on the original PONDEROSA software (Lee et al. in Bioinformatics 27:1727-1728. doi: 10.1093/bioinformatics/btr200, 2011) and includes improved features for structure calculation and refinement. PONDEROSA-C/S consists of three programs: Ponderosa Server, Ponderosa Client, and Ponderosa Analyzer. PONDEROSA-C/S takes as input the protein sequence, a list of assigned chemical shifts, and nuclear Overhauser data sets ((13)C- and/or (15)N-NOESY). The output is a set of assigned NOEs and 3D structural models for the protein. Ponderosa Analyzer supports the visualization, validation, and refinement of the results from Ponderosa Server. These tools enable semi-automated NMR-based structure determination of proteins in a rapid and robust fashion. We present examples showing the use of PONDEROSA-C/S in solving structures of four proteins: two that enable comparison with the original PONDEROSA package, and two from the Critical Assessment of automated Structure Determination by NMR (Rosato et al. in Nat Methods 6:625-626. doi: 10.1038/nmeth0909-625 , 2009) competition. The software package can be downloaded freely in binary format from http://pine.nmrfam.wisc.edu/download_packages.html. Registered users of the National Magnetic Resonance Facility at Madison can submit jobs to the PONDEROSA-C/S server at http://ponderosa.nmrfam.wisc.edu, where instructions, tutorials, and instructions can be found. Structures are normally returned within 1-2 days. PMID:25190042

  4. Structural characterization of C-S-H and C-A-S-H samples-Part I: Long-range order investigated by Rietveld analyses

    SciTech Connect

    Renaudin, Guillaume; Russias, Julie; Leroux, Fabrice; Frizon, Fabien; Cau-dit-Coumes, Celine

    2009-12-15

    Rietveld analyses on samples belonging to C-S-H and C-A-S-H series (0.8<=C/S<=1.7) were realized on X-ray powder patterns. The tobermorite M model was successfully used to refine all the powder patterns from C-S-H samples whatever the C/S value. This gives clear indication on the steady change in a unique structural description, corresponding to a 'tobermorite M defect' model, when passing from C-S-H(I) (C/S<1.0) to C-S-H(II) type (C/S>1.0). The possibility for both C-S-H types (from polymerized silicate chains to isolated silicate dimers) to accommodate the same structural model is explained by the continuous evolution of the occupancies of the cationic sites: the interlayer Ca atoms, the Si atoms from paired and bridging silicates. Accurate refinements of the structural and microstructural parameters evidenced the well crystallized feature of C-S-H phase combined with a small coherent domain size. Insertion of Al atoms in the C-S-H structure (C-A-S-H phase) involves a clear disruption into the layered atomic framework. The large increase of layer spacing observed when incorporating aluminum into C-S-H indicates that Al atoms should be located in the interlayer region of the structure in new crystallographic sites. Aluminum atoms are not substituted silicon crystallographic sites or interlayer calcium crystallographic sites. - Graphical abstract: The Tobermorite M model has been successfully used to perform Rietveld analyses on X-ray powder patterns from C-S-H samples. Refinement of the cationic site occupancies explains the evolution from the linear silicate chains to the isolated silicate dimers when increasing the C/S ratio.

  5. The role of Al in C-S-H: NMR, XRD, and compositional results for precipitated samples

    SciTech Connect

    Sun, G.K.; Young, J. Francis; Kirkpatrick, R. James . E-mail: kirkpat@uiuc.edu

    2006-01-15

    X-ray diffraction, compositional analysis, and {sup 29}Si and {sup 27}Al MAS NMR spectroscopy of Al-substituted tobermorite-type C-S-H made by precipitation from solution provide significant new insight into the structural mechanisms of Al-substitution in this important and complicated phase. Al occurs in 4-, 5-, and 6-coordination (Al[4], Al[5], and Al[6]) and plays multiple structural roles. Al[4] occurs on the bridging tetrahedra of the drierkette Al-silicate chains, and Al[5] and Al[6] occur in the interlayer and perhaps on particle surfaces. Al does not enter either the central Ca-O sheet or the pairing tetrahedra of the tobermorite-type layers. Al[4] occurs on three types of bridging sites, Q{sup 3} sites that bridge across the interlayer; Q{sup 2} sites that are charge balanced by interlayer Ca{sup +2}, Na{sup +}, or H{sup +}; and Q{sup 2} sites that are most likely charge balanced by interlayer or surface Al[5] and Al[6] through Al[4]-O-Al[5,6] linkages. Although the data presented here are for relatively well-crystallized tobermorite-type C-S-H with C/S ratios {<=} 1.2, comparable spectral features for hydrated white cement pastes in previously published papers [M.D. Andersen, H.J. Jakobsen, J. Skibsted, Incorporation of aluminum in the calcium silicate hydrate (C-S-H) of hydrated Portland cements: a high-field {sup 27}Al and {sup 29}Si MAS NMR investigation Inorg. Chem. 42 (2003) 2280-2287; M.D. Andersen, H.J. Jakobsen, J. Skibsted, Characterization of white Portland cement hydration and the C-S-H structure in the presence of sodium aliminate by {sup 27}Al and {sup 29}Si MAS NMR spectroscopy, Cem. Concr. Res. 43 (2004) 857-868; M.D. Andersen, H. J. Jakobsen, J. Skibsted, A new aluminum-hydrate phase in hydrated Portland cements characterized by {sup 27}Al and {sup 29}Si MAS NMR spectroscopy, Cem. Concr. Res., submitted for publication.] indicate the presence of similar structural environments in the C-S-H of such pastes, and by implication OPC pastes.

  6. The C-S-H gel of Portland cement mortars: Part I. The interpretation of energy-dispersive X-ray microanalyses from scanning electron microscopy, with some observations on C-S-H, AFm and AFt phase compositions

    SciTech Connect

    Famy, C.; Brough, A.R.; Taylor, H.F.W

    2003-09-01

    Scanning electron microscopy (SEM) microanalyses of the calcium-silicate-hydrate (C-S-H) gel in Portland cement pastes rarely represent single phases. Essential experimental requirements are summarised and new procedures for interpreting the data are described. These include, notably, plots of Si/Ca against other atom ratios, 3D plots to allow three such ratios to be correlated and solution of linear simultaneous equations to test and quantify hypotheses regarding the phases contributing to individual microanalyses. Application of these methods to the C-S-H gel of a 1-day-old mortar identified a phase with Al/Ca=0.67 and S/Ca=0.33, which we consider to be a highly substituted ettringite of probable composition C{sub 6}A{sub 2}S-bar{sub 2}H{sub 34} or {l_brace}Ca{sub 6}[Al(OH){sub 6}]{sub 2}{center_dot}24H{sub 2}O{r_brace}(SO{sub 4}){sub 2}[Al(OH){sub 4}]{sub 2}. If this is true for Portland cements in general, it might explain observed discrepancies between observed and calculated aluminate concentrations in the pore solution. The C-S-H gel of a similar mortar aged 600 days contained unsubstituted ettringite and an AFm phase with S/Ca=0.125.

  7. Layer-by-Layer Assembled C/S Cathode with Trace Binder for Li-S Battery Application.

    PubMed

    Wang, Qian; Yan, Na; Wang, Meiri; Qu, Chao; Yang, Xiaofei; Zhang, Hongzhang; Li, Xianfeng; Zhang, Huamin

    2015-11-18

    The C/S cathode with only 0.5 wt % binder, composed with Nafion and PVP, was assembled layer-by-layer for lithium-sulfur battery (Li-S) application. It achieved excellent binding strength and battery performance compared to the cathode with 10 wt % PVDF, which is promising to further increase the practical energy density of Li-S batteries. PMID:26541216

  8. C-S@PANI composite with a polymer spherical network structure for high performance lithium-sulfur batteries.

    PubMed

    Wang, Junkai; Yue, Kaiqiang; Zhu, Xiaodan; Wang, Kang L; Duan, Lianfeng

    2016-01-01

    A unique C-S@PANI composite with a conductive polymer spherical network (PSN) has been successfully designed and synthesized by a simple processing approach. The PSN framework is formed at the surface of the oxidized carbon black by conductive polymer self-assembly and grafting, followed by pouring elemental sulfur into the pores of the polymer matrix. As the cathode material for lithium-sulfur batteries, the C-S@PANI composite delivered a high specific capacity of 1453 mA h g(-1) at a 0.1 C current rate and a stable cycling performance of 948 mA h g(-1) after 200 cycles. The composite also demonstrated high capacities of 922 and 581 mA h g(-1) at 50 °C and 0 °C, respectively, after 200 cycles. The conductive PANI coatings were connected with the C-S core-shell composites to form a three-dimensional conducting network, which improves the utilization of the active mass and dual conduction of Li(+) and electrons, while at the same time encapsulating sulfur into the PANI hollow spherical network. The structure effectively inhibits the dissolution and migration of polysulfides into the electrolyte, while improving the cycling stability and the coulombic efficiency of the electrode at high current rates, especially the low temperature electrochemical properties of Li-S batteries. PMID:26608624

  9. C/S algorithm based on properties of dual-polarization radar measurements derived from disdrometer data

    NASA Astrophysics Data System (ADS)

    Adirosi, Elisa; Baldini, Luca; Roberto, Nicoletta; Russo, Fabio

    2016-06-01

    The paper proposes a convective/stratiform (C/S) classification algorithm based on dual-polarization radar measurements obtained from disdrometer measurements through an electromagnetic scattering/extinction model. The drop size distributions, collected by a 2D video disdrometer (2DVD) installed in Rome during HyMeX SOP1, have been used to define the algorithm, and the C-band radar measurements, collected by a Polar 55C, have been analyzed to assess the performance of the proposed method.

  10. Hydrogen induced C-C, C-N, and C-S bond activation on Pt and Ni surfaces

    SciTech Connect

    Gland, J.L.

    1992-01-01

    The work has focussed on hydrogen induced bond activation in adsorbed organic molecules and intermediates containin C-S and C-N and C-C bonds on Ni(100), Ni(111), and Pt(111) surfaces. Fluorescence Yield Near Edge Spectroscopy (FYNES) above the carbon K edge was used for adsorbed organic reactants and in-situ kinetic studies of bond activation. Results indicate that the activation is enhanced on Ni relative to Pt. Methylthiolate and methylamine adsorbed on Pt(111) were studied.

  11. Hydrogen induced C-C, C-N, and C-S bond activation on Pt and Ni surfaces

    SciTech Connect

    Gland, J.L.

    1992-12-01

    The work has focussed on hydrogen induced bond activation in adsorbed organic molecules and intermediates containin C-S and C-N and C-C bonds on Ni(100), Ni(111), and Pt(111) surfaces. Fluorescence Yield Near Edge Spectroscopy (FYNES) above the carbon K edge was used for adsorbed organic reactants and in-situ kinetic studies of bond activation. Results indicate that the activation is enhanced on Ni relative to Pt. Methylthiolate and methylamine adsorbed on Pt(111) were studied.

  12. Copper-Catalyzed Domino Synthesis of 2-Arylthiochromanones through Concomitant C-S Bond Formations Using Xanthate as Sulfur Source.

    PubMed

    Sangeetha, Subramani; Muthupandi, Pandi; Sekar, Govindasamy

    2015-12-18

    An efficient domino process for the synthesis of thioflavanones has been described using a copper catalyst without addition of any external ligand. A variety of thioflavanones have been synthesized from easily accessible 2'-iodochalcones or 2'-bromochalcones in excellent yield through in situ incorporation of sulfur using xanthate as an odorless sulfur source. This domino process proceeds through Cu-catalyzed C(aryl)-S bond formation by the coupling reaction of xanthate with 2'-halochalcones followed by C-S bond cleavage of thioester then S-C bond formation by intramolecular Michael addition. PMID:26642368

  13. Composition, morphology and nanostructure of C-S-H in 70% white Portland cement-30% fly ash blends hydrated at 55 {sup o}C

    SciTech Connect

    Girao, A.V.; Richardson, I.G.; Taylor, R.; Brydson, R.M.D.

    2010-09-15

    Outer product C-S-H had a mixture of fibrillar and foil-like morphology in a 28-day-old water-activated paste, and foil- or lath-like morphology in an alkali-activated paste. It was not possible to determine the chemical composition of C-S-H using SEM-EDX because of fine-scale intermixing with other phases; TEM-EDX was necessary. The C-S-H formed in the alkali-activated paste had a lower mean Ca/(Al + Si) ratio than that formed with water. The mean length of the aluminosilicate anions in the C-S-H was similar in both systems and increased with age; those in the Op C-S-H were likely to be shorter than those present in the Ip C-S-H with water activation, but longer (and more protonated) with alkali. The potassium in the alkali-activated paste was present either within the C-S-H structure charge balancing the substitution of Al{sup 3+} for Si{sup 4+}, or adsorbed on the C-S-H charge balancing sulfate ions.

  14. Regulation of CsrB/C sRNA decay by EIIA(Glc) of the phosphoenolpyruvate: carbohydrate phosphotransferase system.

    PubMed

    Leng, Yuanyuan; Vakulskas, Christopher A; Zere, Tesfalem R; Pickering, Bradley S; Watnick, Paula I; Babitzke, Paul; Romeo, Tony

    2016-02-01

    Csr is a conserved global regulatory system, which uses the sequence-specific RNA-binding protein CsrA to activate or repress gene expression by binding to mRNA and altering translation, stability and/or transcript elongation. In Escherichia coli, CsrA activity is regulated by two sRNAs, CsrB and CsrC, which bind to multiple CsrA dimers, thereby sequestering this protein away from its mRNA targets. Turnover of CsrB/C sRNAs is tightly regulated by a GGDEF-EAL domain protein, CsrD, which targets them for cleavage by RNase E. Here, we show that EIIA(Glc) of the glucose-specific PTS system is also required for the normal decay of these sRNAs and that it acts by binding to the EAL domain of CsrD. Only the unphosphorylated form of EIIA(Glc) bound to CsrD in vitro and was capable of activating CsrB/C turnover in vivo. Genetic studies confirmed that this mechanism couples CsrB/C sRNA decay to the availability of a preferred carbon source. These findings reveal a new physiological influence on the workings of the Csr system, a novel function for the EAL domain, and an important new way in which EIIA(Glc) shapes global regulatory circuitry in response to nutritional status. PMID:26507976

  15. Lithium Sulfur Primary Battery with Super High Energy Density: Based on the Cauliflower-like Structured C/S Cathode

    PubMed Central

    Ma, Yiwen; Zhang, Hongzhang; Wu, Baoshan; Wang, Meiri; Li, Xianfeng; Zhang, Huamin

    2015-01-01

    The lithium-sulfur primary batteries, as seldom reported in the previous literatures, were developed in this work. In order to maximize its practical energy density, a novel cauliflower-like hierarchical porous C/S cathode was designed, for facilitating the lithium-ions transport and sulfur accommodation. This kind of cathode could release about 1300 mAh g−1 (S) capacity at sulfur loading of 6 ~ 14 mg cm−2, and showed excellent shelf stability during a month test at room temperature. As a result, the assembled Li-S soft package battery achieved an energy density of 504 Wh kg−1 (654 Wh L−1), which was the highest value ever reported to the best of our knowledge. This work might arouse the interests on developing primary Li-S batteries, with great potential for practical application. PMID:26456914

  16. ASM Triggered too Observations of 100,000 C/s Black-Hole Candidates (core Program)

    NASA Astrophysics Data System (ADS)

    Resubmission accepted Cycle 2-11 proposal. The PCA is unique by the high count rates (~100.000 c/s) it can record, and its resulting extreme sensitivity to weak variability. Only few sources get this bright. Our RXTE work on Sco X-1 and 1744-28 shows that high count rate observations are very rewarding, but also difficult and not without risk. In the life of the satellite probably only one black hole transient (if any) will reach 10^5 cps/5 PCU levels. When this occurs a window of discovery will be opened on black holes, which will nearly certainly close again within a few days. This proposal aims at ensuring that optimal use is made of this opportunity by performing state of the art high count rate observations covering all of the most crusial aspects of the source variability.

  17. Lithium Sulfur Primary Battery with Super High Energy Density: Based on the Cauliflower-like Structured C/S Cathode

    NASA Astrophysics Data System (ADS)

    Ma, Yiwen; Zhang, Hongzhang; Wu, Baoshan; Wang, Meiri; Li, Xianfeng; Zhang, Huamin

    2015-10-01

    The lithium-sulfur primary batteries, as seldom reported in the previous literatures, were developed in this work. In order to maximize its practical energy density, a novel cauliflower-like hierarchical porous C/S cathode was designed, for facilitating the lithium-ions transport and sulfur accommodation. This kind of cathode could release about 1300 mAh g-1 (S) capacity at sulfur loading of 6 ~ 14 mg cm-2, and showed excellent shelf stability during a month test at room temperature. As a result, the assembled Li-S soft package battery achieved an energy density of 504 Wh kg-1 (654 Wh L-1), which was the highest value ever reported to the best of our knowledge. This work might arouse the interests on developing primary Li-S batteries, with great potential for practical application.

  18. Lithium Sulfur Primary Battery with Super High Energy Density: Based on the Cauliflower-like Structured C/S Cathode.

    PubMed

    Ma, Yiwen; Zhang, Hongzhang; Wu, Baoshan; Wang, Meiri; Li, Xianfeng; Zhang, Huamin

    2015-01-01

    The lithium-sulfur primary batteries, as seldom reported in the previous literatures, were developed in this work. In order to maximize its practical energy density, a novel cauliflower-like hierarchical porous C/S cathode was designed, for facilitating the lithium-ions transport and sulfur accommodation. This kind of cathode could release about 1300 mAh g(-1) (S) capacity at sulfur loading of 6 ~ 14 mg cm(-2), and showed excellent shelf stability during a month test at room temperature. As a result, the assembled Li-S soft package battery achieved an energy density of 504 Wh kg(-1) (654 Wh L(-1)), which was the highest value ever reported to the best of our knowledge. This work might arouse the interests on developing primary Li-S batteries, with great potential for practical application. PMID:26456914

  19. Synthesis and nano-mechanical characterization of calcium-silicate-hydrate (C-S-H) made with 1.5 CaO/SiO{sub 2} mixture

    SciTech Connect

    Foley, Emmy M.; Kim, Jung J.; Reda Taha, M.M.

    2012-09-15

    In this study, calcium silicate hydrate (C-S-H) is synthesized and characterized. C-S-H slurry was made with calcium oxide (CaO) to micro-silica (SiO{sub 2}) mixture ratio of 1.5 and enough deionized water. The slurry was continuously mixed for 7 days, then the excess water was removed. Two methods of drying were implemented: one method used the standard d-dry technique and the other was equilibrated to 11% relative humidity (RH). The dried powders were characterized using thermo gravimetric analysis (TGA), X-ray diffraction analysis (XRDA), and {sup 29}Si magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy. The stoichiometric formulas of synthetic C-S-H powders dried to d-dry and 11% RH in this study were approximated as C{sub 1.2}SH{sub 0.7} and C{sub 1.2}SH{sub 2.4} respectively. The powders were then compacted to create specimens with porosities similar to C-S-H in hydrated cement. The specimens underwent nanoindentation to mechanically characterize C-S-H. The experiments provide insight on the nanoscale mechanical characteristics of C-S-H.

  20. Melting and phase relations in the Fe-C-S-O system at high pressure and temperature

    NASA Astrophysics Data System (ADS)

    Fei, Yingwei

    2010-05-01

    The physical state of the core (liquid outer core and solid inner core) could provide tight constraint on the core temperature if melting temperature of core materials is precisely determined at high pressure. On the other hand, the density of the Earth's core is significantly lower than that of pure iron measured experimentally at high pressure and temperature. The density deficit in the core (both liquid outer core and solid inner core) provides inside into the chemistry of the core, suggesting that the core must contain several weight percent of one or more light elements (lighter than iron) in addition to Fe-Ni alloy. Sulfur (S), carbon (C), and oxygen (O) are the prominent candidates among the proposed light elements, because of their high solar abundance and strong chemical affinity for Fe. Determining the effect of pressure on melting relations in the Fe-S, Fe-C, and Fe-O binary systems and multi-component system is crucial for understanding the chemistry, temperature, and evolution of planetary cores. There has been significant progress in determining the melting relations in the system Fe-FeS at high pressure, using multi-anvil apparatus and laser-heating diamond-anvil cell. These studies have revealed new iron-sulfur compounds (Fe3S2, Fe2S, and Fe3S) stable at high pressures, change of melting relations, and pressure effect on eutectic temperature and composition. The behaviors of the Fe-C and Fe-O systems have also been experimentally investigated recently. Experimental data in the Fe-C-S-O system at high pressure have just emerged. In parallel, there are high-quality data on density measurements of solid and liquid phases at high pressure and temperature. In this study, I present recent advances in experimental techniques and melting relations in the Fe-C-S-O system. The emphasis will be on the need to develop thermodynamic models by synthesis of thermochemical, thermophysical, and phase equilibrium data. The systematic approach provides a better

  1. C-S barrier and vibrational analyses of (halocarbonyl)sulfenyl halides XCO-SX (X = F, Cl, and Br).

    PubMed

    Badawi, Hassan M

    2004-09-01

    The structural stability of (halocarbonyl)sulfenyl halides XCO-SX (X is F, Cl, and Br) was investigated by DFT-B3LYP and ab initio MP2 calculations using 6-311 + G(**) basis set. From the calculations the molecules were found to exist predominantly in the trans conformation (two halogen atoms are trans to each other). Full energy optimizations were carried out for the minima and the transition states (TS) at the two levels, from which the rotational barriers about C-S bond in the three molecules were calculated to be about 12-13 kcal mol(-1). The vibrational frequencies of (fluorocarbonyl)sulfenyl fluoride (FCO-SF), (chlorocarbonyl)-sulfenyl chloride (ClCO-SCl), and (bromocarbonyl)-sulfenyl bromide (BrCO-SBr) were computed at the DFT-B3LYP level and the vibrational assignments for the normal modes of the stable forms of the compounds were made on the basis of normal coordinate calculations and experimental data of the chloride. PMID:15294247

  2. Coupled C-S-Fe geochemistry in a rapidly accumulating marine sedimentary system: Diagenetic and depositional implications

    NASA Astrophysics Data System (ADS)

    Peketi, A.; Mazumdar, A.; Joao, H. M.; Patil, D. J.; Usapkar, A.; Dewangan, P.

    2015-09-01

    In the present study, we have investigated the C-S-Fe systematics in a sediment core (MD161-13) from the Krishna-Godavari (K-G) basin, Bay of Bengal. The core covers the late Holocene period with high overall sedimentation rate of ˜573 cm kyr-1. Pore fluid chemical analyses indicate that the depth of the present sulfate methane transition zone (SMTZ) is at ˜6 mbsf. The (ΔTA + ΔCa + ΔMg)/ΔSO42- ratios suggest that both organoclastic degradation and anaerobic oxidation of methane (AOM) drive sulfate reduction at the study site. The positive correlation between total organic carbon content (TOC) and chromium reducible sulfur (CRS) content indicates marked influence of organoclastic sulfate reduction on sulfidization. Coupled occurrence of 34S-enriched iron sulfide (pyrite) with 12C-enriched authigenic carbonate zones is the possible records of paleo-sulfate methane transition zones where AOM-driven-focused sulfate reduction was likely fueled by sustained high methane flux from underlying gas-rich zone. Aluminum normalized poorly reactive iron (FePR/Al) and La/Yb ratios suggest increasing contribution from Deccan basalts relative to that of Archean-Proterozoic granitic complex in sediment flux of Krishna-Godavari basin during the last 4 kyr.

  3. Metatranscriptomic evidence of pervasive and diverse chemolithoautotrophy relevant to C, S, N and Fe cycling in a shallow alluvial aquifer

    PubMed Central

    Jewell, Talia N M; Karaoz, Ulas; Brodie, Eoin L; Williams, Kenneth H; Beller, Harry R

    2016-01-01

    Groundwater ecosystems are conventionally thought to be fueled by surface-derived allochthonous organic matter and dominated by heterotrophic microbes living under often-oligotrophic conditions. However, in a 2-month study of nitrate amendment to a perennially suboxic aquifer in Rifle (CO), strain-resolved metatranscriptomic analysis revealed pervasive and diverse chemolithoautotrophic bacterial activity relevant to C, S, N and Fe cycling. Before nitrate injection, anaerobic ammonia-oxidizing (anammox) bacteria accounted for 16% of overall microbial community gene expression, whereas during the nitrate injection, two other groups of chemolithoautotrophic bacteria collectively accounted for 80% of the metatranscriptome: (1) members of the Fe(II)-oxidizing Gallionellaceae family and (2) strains of the S-oxidizing species, Sulfurimonas denitrificans. Notably, the proportion of the metatranscriptome accounted for by these three groups was considerably greater than the proportion of the metagenome coverage that they represented. Transcriptional analysis revealed some unexpected metabolic couplings, in particular, putative nitrate-dependent Fe(II) and S oxidation among nominally microaerophilic Gallionellaceae strains, including expression of periplasmic (NapAB) and membrane-bound (NarGHI) nitrate reductases. The three most active groups of chemolithoautotrophic bacteria in this study had overlapping metabolisms that allowed them to occupy different yet related metabolic niches throughout the study. Overall, these results highlight the important role that chemolithoautotrophy can have in aquifer biogeochemical cycling, a finding that has broad implications for understanding terrestrial carbon cycling and is supported by recent studies of geochemically diverse aquifers. PMID:26943628

  4. Metatranscriptomic evidence of pervasive and diverse chemolithoautotrophy relevant to C, S, N and Fe cycling in a shallow alluvial aquifer.

    PubMed

    Jewell, Talia N M; Karaoz, Ulas; Brodie, Eoin L; Williams, Kenneth H; Beller, Harry R

    2016-09-01

    Groundwater ecosystems are conventionally thought to be fueled by surface-derived allochthonous organic matter and dominated by heterotrophic microbes living under often-oligotrophic conditions. However, in a 2-month study of nitrate amendment to a perennially suboxic aquifer in Rifle (CO), strain-resolved metatranscriptomic analysis revealed pervasive and diverse chemolithoautotrophic bacterial activity relevant to C, S, N and Fe cycling. Before nitrate injection, anaerobic ammonia-oxidizing (anammox) bacteria accounted for 16% of overall microbial community gene expression, whereas during the nitrate injection, two other groups of chemolithoautotrophic bacteria collectively accounted for 80% of the metatranscriptome: (1) members of the Fe(II)-oxidizing Gallionellaceae family and (2) strains of the S-oxidizing species, Sulfurimonas denitrificans. Notably, the proportion of the metatranscriptome accounted for by these three groups was considerably greater than the proportion of the metagenome coverage that they represented. Transcriptional analysis revealed some unexpected metabolic couplings, in particular, putative nitrate-dependent Fe(II) and S oxidation among nominally microaerophilic Gallionellaceae strains, including expression of periplasmic (NapAB) and membrane-bound (NarGHI) nitrate reductases. The three most active groups of chemolithoautotrophic bacteria in this study had overlapping metabolisms that allowed them to occupy different yet related metabolic niches throughout the study. Overall, these results highlight the important role that chemolithoautotrophy can have in aquifer biogeochemical cycling, a finding that has broad implications for understanding terrestrial carbon cycling and is supported by recent studies of geochemically diverse aquifers. PMID:26943628

  5. Catalytic C-N, C-O, and C-S Bond Formation Promoted by Organoactinide Complexes

    NASA Astrophysics Data System (ADS)

    Eisen, Moris S.

    Throughout this last decade, we have witnessed impressively how the chemistry of electrophilic d0/fn actinides has been prospering either in their new synthetic approaches reaching very interesting compounds or in their use in stoichiometric and catalytic reactions leading to high levels of complexity. The unique rich and complex features of organoactinides prompted the development of this field toward catalysis in demanding chemical transformations. In this review, we present a brief and selective survey of the recent developments in homogenous catalysis of organoactinide complexes, especially toward the formation of new C-N, C-O, and C-S bonds. We start by presenting the synthesis and characterization of the corresponding organoactinide complexes, followed by the homogeneous catalytic chemical transformations that include the hydroamination of terminal alkynes, the polymerization of ɛ-caprolactone and L-lactide, the reduction of azides and hydrazines by high-valent organouranium complexes, the hydrothiolation of terminal alkynes, and the catalytic Tishchenko reaction. For each reaction, the scope and the thermodynamic, kinetic, and mechanistic aspects are presented.

  6. Hydrodesulfurization on Transition Metal Catalysts: Elementary Steps of C-S Bond Activation and Consequences of Bifunctional Synergies

    NASA Astrophysics Data System (ADS)

    Yik, Edwin Shyn-Lo

    The presence of heteroatoms (e.g. S, N) in crude oil poses formidable challenges in petroleum refining processes as a result of their irreversible binding on catalytically active sites at industrially relevant conditions. With increasing pressures from legislation that continues to lower the permissible levels of sulfur content in fuels, hydrodesulfurization (HDS), the aptly named reaction for removing heteroatoms from organosulfur compounds, has become an essential feedstock pretreatment step to remove deleterious species from affecting downstream processing. Extensive research in the area has identified the paradigm catalysts for desulfurization; MoSx or WSx, promoted with Co or Ni metal; however, despite the vast library of both empirical and fundamental studies, a clear understanding of site requirements, the elementary steps of C-S hydrogenolysis, and the properties that govern HDS reactivity and selectivity have been elusive. While such a lack of rigorous assessments has not prevented technological advancements in the field of HDS catalysis, fundamental interpretations can inform rational catalyst and process design, particularly in light of new requirements for "deep" desulfurization and in the absence of significant hydrotreatment catalyst developments in recent decades. We report HDS rates of thiophene, which belongs to a class of compounds that are most resistant to sulfur removal (i.e. substituted alkyldibenzothiophenes), over a range of industrially relevant temperatures and pressures, measured at differential conditions and therefore revealing their true kinetic origins. These rates, normalized by the number of exposed metal atoms, on various SiO 2-supported, monometallic transition metals (Re, Ru, Pt), range several orders of magnitude. Under relevant HDS conditions, Pt and Ru catalysts form a layer of chemisorbed sulfur on surfaces of a metallic bulk, challenging reports that assume the latter exists as its pyrite sulfide phase during reaction. While

  7. Metatranscriptomic Evidence of Chemolithoautotrophy in the Rifle (CO) Subsurface Relevant to C, S, N, and Fe Cycling

    NASA Astrophysics Data System (ADS)

    Beller, H. R.; Jewell, T. N. M.; Karaoz, U.; Thomas, B. C.; Banfield, J. F.; Brodie, E.; Williams, K. H.

    2014-12-01

    Although there is a limited understanding of the chemolithoautotrophic activity of aquifer microorganisms, such subsurface microbial activity could greatly influence the cycling of elements such as C, S, N, and Fe. Here, we present transcriptional (RNA-Seq) evidence of the emergence of such chemolithoautotrophic activities in groundwater filter samples from a 2-month experiment in which up to 1.5 mM nitrate (a native electron acceptor) was injected into a perennially suboxic/anoxic aquifer (Rifle, CO) containing a large reservoir of reduced Fe- and S-containing compounds. Illumina sequence data from rRNA-subtracted cDNA libraries was assembled and mapped to phylogenetically binned Rifle metagenome data. Indicative of the activity of Fe(II)-oxidizing bacteria, many high-abundance transcripts mapped to the Gallionellaceae family, whose known members are chemolithoautotrophic bacteria that catalyze Fe(II) oxidation. For example, included among the most abundant transcripts were a cold-shock protein and an acyl carrier protein with 96-98% protein sequence identity to Gallionella capsiferriformans and a nitrite reductase (nirS) gene likely belonging to a Sideroxydans relative. The apparent activity of Gallionellaceae members is consistent with 16S rRNA iTag analyses of these samples, which indicated that Gallionella-related taxa accounted for up to ~50% of these communities. Evidence of sulfide oxidation also was apparent in these samples. For example, highly expressed subunits of APS reductase were very similar to those of the obligately chemolithoautotrophic S- and Fe(II)-oxidizing Thiobacillus denitrificans in terms of sequence identity (98-99%) and synteny of the mapped scaffold. Also highly expressed were a ß-Proteobacterial Form II RubisCO gene and a hydrazine oxidoreductase gene (93% identity to the planctomycete KSU-1), the latter strongly indicative of anaerobic ammonia oxidation (anammox) activity, which has seldom been reported in aquifer environments. Such

  8. Hydrodesulfurization on Transition Metal Catalysts: Elementary Steps of C-S Bond Activation and Consequences of Bifunctional Synergies

    NASA Astrophysics Data System (ADS)

    Yik, Edwin Shyn-Lo

    The presence of heteroatoms (e.g. S, N) in crude oil poses formidable challenges in petroleum refining processes as a result of their irreversible binding on catalytically active sites at industrially relevant conditions. With increasing pressures from legislation that continues to lower the permissible levels of sulfur content in fuels, hydrodesulfurization (HDS), the aptly named reaction for removing heteroatoms from organosulfur compounds, has become an essential feedstock pretreatment step to remove deleterious species from affecting downstream processing. Extensive research in the area has identified the paradigm catalysts for desulfurization; MoSx or WSx, promoted with Co or Ni metal; however, despite the vast library of both empirical and fundamental studies, a clear understanding of site requirements, the elementary steps of C-S hydrogenolysis, and the properties that govern HDS reactivity and selectivity have been elusive. While such a lack of rigorous assessments has not prevented technological advancements in the field of HDS catalysis, fundamental interpretations can inform rational catalyst and process design, particularly in light of new requirements for "deep" desulfurization and in the absence of significant hydrotreatment catalyst developments in recent decades. We report HDS rates of thiophene, which belongs to a class of compounds that are most resistant to sulfur removal (i.e. substituted alkyldibenzothiophenes), over a range of industrially relevant temperatures and pressures, measured at differential conditions and therefore revealing their true kinetic origins. These rates, normalized by the number of exposed metal atoms, on various SiO 2-supported, monometallic transition metals (Re, Ru, Pt), range several orders of magnitude. Under relevant HDS conditions, Pt and Ru catalysts form a layer of chemisorbed sulfur on surfaces of a metallic bulk, challenging reports that assume the latter exists as its pyrite sulfide phase during reaction. While

  9. Management of a Septic Open Abdomen Patient with Spontaneous Jejunal Perforation after Emergent C/S with Confounding Factor of Mild Acute Pancreatitis

    PubMed Central

    Yetisir, Fahri; Sarer, Akgün Ebru; Acar, Hasan Zafer; Osmanoglu, Gokhan; Özer, Mehmet; Yaylak, Faik

    2016-01-01

    Introduction. We report the management of a septic Open Abdomen (OA) patient by the help of negative pressure therapy (NPT) and abdominal reapproximation anchor (ABRA) system in pregnant woman with spontaneous jejunal perforation after emergent cesarean section (C/S) with confounding factor of mild acute pancreatitis (AP). Presentation of Case. A 29-year-old and 34-week pregnant woman with AP underwent C/S. She was arrested after anesthesia induction and responded to cardiopulmonary resuscitation (CPR). There were only ash-colored serosanguinous fluid within abdomen during C/S. After C/S, she was transferred to intensive care unit (ICU) with vasopressor support. On postoperative 1st day, she underwent reoperation due to fecal fluid coming near the drainage. Leakage point could not be identified exactly and operation had to be deliberately abbreviated due to hemodynamic instability. NPT was applied. Two days later source control was provided by conversion of enteroatmospheric fistula (EAF) to jejunostomy. ABRA was added and OA was closed. No hernia developed at 10-month follow-up period. Conclusion. NPT application in septic OA patient may gain time to patient until adequate source control could be achieved. Using ABRA in conjunction with NPT increases the fascial closure rate in infected OA patient. PMID:27006853

  10. The phylogeny of C/S1 bZIP transcription factors reveals a shared algal ancestry and the pre-angiosperm translational regulation of S1 transcripts

    PubMed Central

    Peviani, Alessia; Lastdrager, Jeroen; Hanson, Johannes; Snel, Berend

    2016-01-01

    Basic leucine zippers (bZIPs) form a large plant transcription factor family. C and S1 bZIP groups can heterodimerize, fulfilling crucial roles in seed development and stress response. S1 sequences also harbor a unique regulatory mechanism, termed Sucrose-Induced Repression of Translation (SIRT). The conservation of both C/S1 bZIP interactions and SIRT remains poorly characterized in non-model species, leaving their evolutionary origin uncertain and limiting crop research. In this work, we explored recently published plant sequencing data to establish a detailed phylogeny of C and S1 bZIPs, investigating their intertwined role in plant evolution, and the origin of SIRT. Our analyses clarified C and S1 bZIP orthology relationships in angiosperms, and identified S1 sequences in gymnosperms. We experimentally showed that the gymnosperm orthologs are regulated by SIRT, tracing back the origin of this unique regulatory mechanism to the ancestor of seed plants. Additionally, we discovered an earlier S ortholog in the charophyte algae Klebsormidium flaccidum, together with a C ortholog. This suggests that C and S groups originated by duplication from a single algal proto-C/S ancestor. Based on our observations, we propose a model wherein the C/S1 bZIP dimer network evolved in seed plants from pre-existing C/S bZIP interactions. PMID:27457880

  11. A Comparison of Positive Outcome Expectancies: A Review of the Theories of M. F. Scheier, C. S. Carver, M. E. P. Seligman, and C. R. Snyder.

    ERIC Educational Resources Information Center

    Bird, William A.

    Research has shown that optimistic and pessimistic outcome expectancy evaluations are associated with adaptive and maladaptive levels of psychological functioning, physical wellness, and health recovery issues. The research of M. F. Scheier, C. S. Carver, M. E. P. Seligman, and C. R. Snyder supports the hypothesis that elevated optimism or…

  12. Application of Thio-Ugi Adducts for the Preparation of Benzo[b]thiophene and S-Heterocycle Library via Copper Catalyzed Intramolecular C-S Bond Formation.

    PubMed

    Kim, Yong-Sang; Kwak, Se Hun; Gong, Young-Dae

    2015-06-01

    Fused heterocycles, such as benzo[b]thiophene, thiochroman, benzo[b][1,4]thiazine, and 1,4-benzothiazepine were generated from thio-Ugi adducts containing a thioamide group through copper-catalyzed intramolecular C-S bond formation under microwave irradiation. PMID:25961783

  13. Structural and nano-mechanical properties of Calcium Silicate Hydrate (C-S-H) formed from alite hydration in the presence of sodium and potassium hydroxide

    SciTech Connect

    Mendoza, Oscar; Giraldo, Carolina; Camargo, Sergio S.

    2015-08-15

    This research evaluates the effect of sodium and potassium hydroxide on the structure and nano-mechanical properties of Calcium Silicate Hydrate (C-S-H) formed from the hydration of pure alite. Monoclinic (MIII) alite was synthesized and hydrated, using water-to-alite ratios of 0.5 and 0.6 and additions of 10% NaOH and KOH by weight of alite. Based on results of X-ray diffraction, isothermal calorimetry, thermogravimetric analysis, Nuclear Magnetic Resonance and nanoindentation, two different effects of the alkaline hydroxides on the hydration reaction of alite, both at early and later ages, can be identified: (i) a differentiated hydration process, attributed to an enhancement in calcium hydroxide (CH) precipitation and a stimulation of the C-S-H nuclei; and (ii) an increase in the elastic modulus of the C-S-H aggregations, attributed to an electrostatic attraction between positive charges from the alkaline cations and negative charges from the C-S-H structure.

  14. The phylogeny of C/S1 bZIP transcription factors reveals a shared algal ancestry and the pre-angiosperm translational regulation of S1 transcripts.

    PubMed

    Peviani, Alessia; Lastdrager, Jeroen; Hanson, Johannes; Snel, Berend

    2016-01-01

    Basic leucine zippers (bZIPs) form a large plant transcription factor family. C and S1 bZIP groups can heterodimerize, fulfilling crucial roles in seed development and stress response. S1 sequences also harbor a unique regulatory mechanism, termed Sucrose-Induced Repression of Translation (SIRT). The conservation of both C/S1 bZIP interactions and SIRT remains poorly characterized in non-model species, leaving their evolutionary origin uncertain and limiting crop research. In this work, we explored recently published plant sequencing data to establish a detailed phylogeny of C and S1 bZIPs, investigating their intertwined role in plant evolution, and the origin of SIRT. Our analyses clarified C and S1 bZIP orthology relationships in angiosperms, and identified S1 sequences in gymnosperms. We experimentally showed that the gymnosperm orthologs are regulated by SIRT, tracing back the origin of this unique regulatory mechanism to the ancestor of seed plants. Additionally, we discovered an earlier S ortholog in the charophyte algae Klebsormidium flaccidum, together with a C ortholog. This suggests that C and S groups originated by duplication from a single algal proto-C/S ancestor. Based on our observations, we propose a model wherein the C/S1 bZIP dimer network evolved in seed plants from pre-existing C/S bZIP interactions. PMID:27457880

  15. An investigation of the structure and phase relations of C-S-H gels. Final report, August 15, 1991--September 14, 1997

    SciTech Connect

    Grutzeck, M.W.; Benesi, A.

    1997-12-14

    Solid state NMR was used to obtain data on the atomic level structure of calcium silicate hydrate (C-S-H) that formed from a variety of starting materials under a variety of conditions. Because C-S-H is the major component of hydrated portland cement, a knowledge of its structure and of its structural evolution will ultimately allow users of cement containing materials such as mortars and concrete to more accurately predict the physical and mechanical behavior of these materials once they are placed into service. From the outset, the goal of the work was to observe the hydration process on the atomic level, integrate the findings with existing data in the literature, and refine hydration models as necessary to accommodate the newly acquired data.

  16. Copper-catalyzed aerobic oxidation and cleavage/formation of C-S bond: a novel synthesis of aryl methyl sulfones from aryl halides and DMSO.

    PubMed

    Yuan, Gaoqing; Zheng, Junhua; Gao, Xiaofang; Li, Xianwei; Huang, Liangbin; Chen, Huoji; Jiang, Huanfeng

    2012-08-01

    With atmospheric oxygen as the oxidant, a novel copper(I)-catalyzed synthesis of aryl methyl sulfones from aryl halides and widely available DMSO is described. The procedure tolerates aryl halides with various functional groups (such as methoxy, acetyl, chloro, fluoro and nitro groups), which could afford aryl methyl sulfones in moderate to high yields. The copper-catalyzed aerobic oxidation and the cleavage/formation of C-S bond are the key steps for this transformation. PMID:22728918

  17. Cu(II)-mediated C-S/N-S bond formation via C-H activation: access to benzoisothiazolones using elemental sulfur.

    PubMed

    Chen, Fa-Jie; Liao, Gang; Li, Xin; Wu, Jun; Shi, Bing-Feng

    2014-11-01

    A copper-mediated C-S/N-S bond-forming reaction via C-H activation that uses elemental sulfur has been developed. The addition of TBAI was found to be crucial for the success of this transformation. The method is scalable, shows excellent functional group tolerance, and is compatible with heterocycle substrates, providing efficient and practical access to benzoisothiazolones. The direct diversification of the benzoisothiazolone products into a variety of sulfur-containing compounds is also demonstrated. PMID:25325568

  18. I/S and C/S mixed layers, some indicators of recent physical-chemical changes in active geothermal systems: The case study of Chipilapa (El Salvador)

    SciTech Connect

    Beaufort, D.; Papapanagiotou, P.; patrier, P.; Fouillac, A.M.; Traineau, H.

    1996-01-24

    I/S and C/S mixed layers from the geothermal field of Chipilapa (El Salvador) have been studied in details in order to reevaluate their potential use as indicator of the thermodynamic conditions in which they were formed. It is funded that overprinting of clay bearing alteration stages is common. For a given alteration stage, the spatial variation of I/S and C/S mixed layer ininerals is controlled by kinetics of mixed layer transformation and not only by temperature. Clay geo-thermometers cannot give reliable results because the present crystal-chemical states of the I/S and C/S mixed layers is not their initial state, it was aquired during the overall hydrothermal history which post dated the nucleation of smectitic clay material at high temperature. Occurrences of smectites or smectite-rich mixed layers at high temperature in reservoirs is a promising guide for reconstruct the zones in which boiling or mixing of non isotherinal fluids occurred very recently or still presently.

  19. Modifications of the C-S-H gel by hydration at 40{sup o}C of belite cements from coal fly ash class C

    SciTech Connect

    Goni, S.; Guerrero, A.

    2008-01-15

    Abstract: The influence of the temperature on two types of hydrated fly ash belite cement (FABC) pastes were investigated at a nanoscale (1-100 nm) by measuring the specific surface area and pore-size distribution by the sorption isotherms of nitrogen gas and the BET method, and at a microscale from the pore-size distribution measured by mercury intrusion porosimetry. The two belite cements were fabricated by the hydrothermal-calcination route of fly ash class C in NaOH 1M solution (FABC-2-N) and demineralized water (FABC-2-W). In the case of FABC-2-W, a densification of the C-S-H gel was produced at the temperature of 40{sup o}C, which favored the formation of pores about 3 nm in diameter leading to higher surface area values, compared with the C-S-H gel formed at 20{sup o}C. At a microscale, the temperature led to an increase of capillary porosity (>0.05 {mu} m) at a later age of hydration and, consequently, a decrease of compressive mechanical strength. In the case of FABC-2-N, the densification of the gel was less evident, but the increase of capillary porosity (pores of diameter >0.05 {mu} m) was higher. Significant direct linear quantitative correlations were found among these nanostructure characteristics of the C-S-H gel and macrostructural engineering property such as the compressive mechanical strength, for the two FABC-2-W and FABC-2-N cements under normal conditions. At 40{sup o}C, the correlations were not so clear probably due to another microstructural factor such as the increase of the larger capillary porosity (>0.05 {mu} m).

  20. Effects of carbon-to-sulfur (C/S) ratio and nitrate (N) dosage on Denitrifying Sulfur cycle-associated Enhanced Biological Phosphorus Removal (DS-EBPR)

    PubMed Central

    Yu, Mei; Lu, Hui; Wu, Di; Zhao, Qing; Meng, Fangang; Wang, Yudan; Hao, Xiaodi; Chen, Guang-Hao

    2016-01-01

    In this study, the Denitrifying Sulfur cycle-associated Enhanced Biological Phosphorous Removal (DS-EBPR) with 20 mg P/L/d of the volumetric P removal rate was successfully achieved in a Sequencing Batch Reactor (SBR). The effects of carbon-to-sulfur (C/S) mass ratio and nitrate (N) dosage were investigated through two batch tests to reveal the role of wastewater compositions in DS-EBPR performance. The optimal specific P release and uptake rates (0.4 and 2.4 mg P/g VSS/h, respectively) were achieved at C/S/P/N mass ratio of 150/200/20/20, and poly-S is supplied as a potential electron and energy storage. The nitrate dosage in a range of 10–50 mg N/L had no significant influence on P uptake rates (2.1 ~ 2.4 mg P/g VSS/h), but significantly affected the storage of inclusion poly-S, the poly-S oxidation rate was increased about 16% while dosing nitrate from 20 to 30 mg N/L. It implies that nitrate is denitrified in the P uptake phase, and excess nitrate is further consumed by poly-S. Moreover, the microbial analysis showed that the functional bacteria should mostly belong to denitrifying bacteria or Unclassified genera. PMID:26983801

  1. Early Permian extensional shearing of an Ordovician granite: The Saint-Eutrope "C/S-like" orthogneiss (Montagne Noire, French Massif Central)

    NASA Astrophysics Data System (ADS)

    Pitra, Pavel; Poujol, Marc; Van Den Driessche, Jean; Poilvet, Jean-Charles; Paquette, Jean-Louis

    2012-08-01

    Dating the magmatic events in the Montagne Noire gneiss dome is a key point to arbitrate between the different interpretations of the Late Carboniferous-Early Permian tectonics in this southern part of the Variscan belt. The Saint-Eutrope orthogneiss crops out along the northern flank of the dome. We show that the protolith of this orthogneiss is an Ordovician granite dated at 455 ± 2 Ma (LA-ICP-MS U-Pb dating on zircon). This age is identical to that previously obtained on the augen orthogneiss of the southern flank, strongly suggesting that both orthogneiss occurrences have the same Ordovician protolith. The Saint-Eutrope orthogneiss experienced intense shearing along the Espinouse extensional detachment at ca. 295 Ma (LA-ICP-MS U-Pb-Th on monazite), an age close to that determined previously on mica by the 39Ar-40Ar method and contemporaneous with the emplacement age of the syntectonic Montalet granite farther to the west. This normal sense shearing reworked previous fabrics related to Variscan thrusting that can be still observed in the augen orthogneiss of the southern flank, and is responsible for the spectacular "C/S-like" pattern of the Saint-Eutrope orthogneiss. This work also shows that care is needed when dealing with C/S-type structures, since they can develop not only in syntectonic intrusions, but also in orthogneisses affected by an intense secondary deformation, at decreasing temperature.

  2. Effects of carbon-to-sulfur (C/S) ratio and nitrate (N) dosage on Denitrifying Sulfur cycle-associated Enhanced Biological Phosphorus Removal (DS-EBPR)

    NASA Astrophysics Data System (ADS)

    Yu, Mei; Lu, Hui; Wu, Di; Zhao, Qing; Meng, Fangang; Wang, Yudan; Hao, Xiaodi; Chen, Guang-Hao

    2016-03-01

    In this study, the Denitrifying Sulfur cycle-associated Enhanced Biological Phosphorous Removal (DS-EBPR) with 20 mg P/L/d of the volumetric P removal rate was successfully achieved in a Sequencing Batch Reactor (SBR). The effects of carbon-to-sulfur (C/S) mass ratio and nitrate (N) dosage were investigated through two batch tests to reveal the role of wastewater compositions in DS-EBPR performance. The optimal specific P release and uptake rates (0.4 and 2.4 mg P/g VSS/h, respectively) were achieved at C/S/P/N mass ratio of 150/200/20/20, and poly-S is supplied as a potential electron and energy storage. The nitrate dosage in a range of 10–50 mg N/L had no significant influence on P uptake rates (2.1 ~ 2.4 mg P/g VSS/h), but significantly affected the storage of inclusion poly-S, the poly-S oxidation rate was increased about 16% while dosing nitrate from 20 to 30 mg N/L. It implies that nitrate is denitrified in the P uptake phase, and excess nitrate is further consumed by poly-S. Moreover, the microbial analysis showed that the functional bacteria should mostly belong to denitrifying bacteria or Unclassified genera.

  3. Effects of carbon-to-sulfur (C/S) ratio and nitrate (N) dosage on Denitrifying Sulfur cycle-associated Enhanced Biological Phosphorus Removal (DS-EBPR).

    PubMed

    Yu, Mei; Lu, Hui; Wu, Di; Zhao, Qing; Meng, Fangang; Wang, Yudan; Hao, Xiaodi; Chen, Guang-Hao

    2016-01-01

    In this study, the Denitrifying Sulfur cycle-associated Enhanced Biological Phosphorous Removal (DS-EBPR) with 20 mg P/L/d of the volumetric P removal rate was successfully achieved in a Sequencing Batch Reactor (SBR). The effects of carbon-to-sulfur (C/S) mass ratio and nitrate (N) dosage were investigated through two batch tests to reveal the role of wastewater compositions in DS-EBPR performance. The optimal specific P release and uptake rates (0.4 and 2.4 mg P/g VSS/h, respectively) were achieved at C/S/P/N mass ratio of 150/200/20/20, and poly-S is supplied as a potential electron and energy storage. The nitrate dosage in a range of 10-50 mg N/L had no significant influence on P uptake rates (2.1 ~ 2.4 mg P/g VSS/h), but significantly affected the storage of inclusion poly-S, the poly-S oxidation rate was increased about 16% while dosing nitrate from 20 to 30 mg N/L. It implies that nitrate is denitrified in the P uptake phase, and excess nitrate is further consumed by poly-S. Moreover, the microbial analysis showed that the functional bacteria should mostly belong to denitrifying bacteria or Unclassified genera. PMID:26983801

  4. D.C.'s Braveheart

    ERIC Educational Resources Information Center

    Kronholz, June

    2010-01-01

    This article discusses Michelle Rhee's style of leadership--as steely as the sound of her peekaboo high heels on a linoleum-tile hallway--which has angered much of Washington, D.C., and baffled the rest since she arrived as schools chancellor in June 2007. But it is also helping her gain control of a school system that has defied management for…

  5. Volatile compounds of sulfur in the Fe-C-S system at 5.3 GPa and 1300°C

    NASA Astrophysics Data System (ADS)

    Zhimulev, E. I.; Sonin, V. M.; Bul'bak, T. A.; Chepurov, A. I.; Tomilenko, A. A.; Pokhilenko, N. P.

    2015-05-01

    This report presents the results of experimental studies of the fluid phase in the Fe-C-S system at high P and T values (5.3 GPa and 1300°C) conforming to diamond synthesis. The samples for experiments were mounted on air; therefore, the volatile compounds detected after the experiments are characterized by a wide variety and complicated composition involving both inorganic and organic components. Among the inorganic compounds, CO2, H2O, N2, SO2, CS2, and COS were detected. The GC/MS analysis revealed hydrocarbons (paraffins, olefins, and arenes), including high-molecular compounds. The formation of heavy hydrocarbons confirms their thermodynamic stability under high pressure. Oxygenated hydrocarbons (alcohols, aldehydes, ketones, carboxylic acids, and ethers) were also detected.

  6. Dissolution rates of coals and graphite in Fe-C-S melts in direct ironmaking: Influence of melt carbon and sulfur on carbon dissolution

    NASA Astrophysics Data System (ADS)

    Wu, C.; Sahajwalla, V.

    2000-04-01

    Carbon dissolution from graphite and coals was investigated by using a carburizer cover technique in an induction furnace. The intent of the study was to investigate the influence of factors governing the rate of carbon dissolution from carbonaceous materials, especially coals, into Fe-C-S melts. The factors studied were the initial melt carbon and sulfur concentrations and the wettability between carbonaceous materials and the melt. It was found that graphite dissolves markedly faster than coal. The rate of carbon dissolution from graphite could be decreased by increasing the sulfur in the melt. Also, poor wetting could retard the rate of carbon dissolution by reducing the surface area for mass transfer. Carbon dissolution from graphite is controlled by mass transfer in the liquid boundary layer adjacent to the solid/liquid interface. The rate of carbon dissolution from coal is more sensitive to the molten iron composition. A higher initial melt carbon and sulfur content retards the rate of carbon dissolution from coal more significantly than from graphite. However, the rate constant of coal char dissolution does not show a strong dependence on the wettability. Carbon dissolution from coals is most likely governed by a mixed-control mechanism that includes liquid-side mass transfer. The mechanisms underlying the influence of bath sulfur on carbon dissolution from graphite and coals are discussed.

  7. Density and water content of nanoscale solid C-S-H formed in alkali-activated slag (AAS) paste and implications for chemical shrinkage

    SciTech Connect

    Thomas, Jeffrey J.; Allen, Andrew J.; Jennings, Hamlin M.

    2012-02-15

    Alkali-activated slag (AAS) paste was analyzed using small-angle neutron scattering (SANS). The scattering response indicates that the microstructure consists of a uniform matrix of hydration product with a high surface area studded with unhydrated cores of slag particles. In contrast with portland cement paste, no surface fractal scattering regime was detected, and elevated temperature curing (at 60 Degree-Sign C) had no detectable effect on the microstructure at any length scale studied. The specific surface area of the AAS pastes is about 25% higher than that of a portland cement paste cured under the same conditions. The composition and mass density of the nanoscale solid C-S-H phase formed in the AAS paste was determined using a previously developed neutron scattering method, in conjunction with a hydration model. The result ((CaO){sub 0.99}-SiO{sub 2}-(Al{sub 2}O{sub 3}){sub 0.06}-(H{sub 2}O){sub 0.97}, d = (2.73 {+-} 0.02) g/cm{sup 3}) is significantly lower in calcium and in water as compared to portland cement or pure tricalcium silicate paste. These values were used to calculate the chemical shrinkage that would result from complete hydration of the AAS paste. The result, (12.2 {+-} 1.5) cm{sup 3} of volumetric shrinkage per 100 g of unhydrated cement, is about twice the amount of chemical shrinkage exhibited by normal cement pastes.

  8. Optimum calcination temperature in the synthesis of a N-C-S co-doped TiO2 photocatalyst, as monitored by neutron diffraction

    NASA Astrophysics Data System (ADS)

    Rozas, Francisco; Bengtsson, Nicklas; Fabelo, Oscar; Puente, Inés; Castellote, Marta

    2014-11-01

    Calcination of a co-doped (N-C-S) TiO2 photocatalyst has been done following the whole process by neutron diffraction (instrument D1B of the ILL) with the objective of study the transition between two crystalline phases: anatase and rutile in order to find the optimum temperature leading to the coexistence of both for this catalyst whose band gap has been shifted to give activity in the visible part of the electromagnetic spectrum. This coexistence is important as it has been established that these catalyst are more efficient than those having only one individual phase. At this respect, it is very important to find the optimum temperature at with synthesis has to be done. In this research it was established that at the heating ramp of 17°C/5 min, the coexistence of both crystalline phases took place within a narrow margin of temperatures between 610°C and 690°C. At higher temperatures only rutile can be identified as the crystalline phase of the TiO2.

  9. Synthesis of 1,2,4-Triazoles via Oxidative Heterocyclization: Selective C-N Bond Over C-S Bond Formation.

    PubMed

    Gogoi, Anupal; Guin, Srimanta; Rajamanickam, Suresh; Rout, Saroj Kumar; Patel, Bhisma K

    2015-09-18

    The higher propensity of C-N over C-S bond forming ability was demonstrated, through formal C-H functionalization during the construction of 4,5-disubstituted 1,2,4-triazole-3-thiones from arylidenearylthiosemicarbazides catalyzed by Cu(II). However, steric factors imparted by the o-disubstituted substrates tend to change the reaction path giving thiodiazole as the major or an exclusive product. Upon prolonging the reaction time, the in situ generated thiones are transformed to 4,5-disubstituted 1,2,4-triazoles via a desulfurization process. Two classes of heterocycles viz. 4,5-disubstituted 1,2,4-triazole-3-thiones and 4,5-disubstituted 1,2,4-triazoles can be synthesized from arylidenearylthiosemicarbazides by simply adjusting the reaction time. Desulfurization of 1,2,4-triazole-3-thiones is assisted by thiophilic Cu to provide 1,2,4-triazoles with concomitant formation of CuS and polynuclear sulfur anions as confirmed from scanning electron microscope and energy dispersive X-ray spectroscopy measurements. A one-pot synthesis of an antimicrobial compound has been successfully achieved following this strategy. PMID:26332253

  10. Disposition of S-1108, a new oral cephem antibiotic, and metabolic fate of pivalic acid liberated from [pivaloyl-14C]S-1108 in rats and dogs.

    PubMed Central

    Mizojiri, K; Futaguchi, S; Norikura, R; Katsuyama, Y; Nagasaki, T; Yoshimori, T; Nakanishi, M

    1995-01-01

    [pivaloyl-14C]S-1108, which is 14C labeled at the pivalic acid moiety of the pivaloyloxymethyl side chain of S-1108, was administered orally to rats and dogs, and the disposition of pivalic acid cleft from S-1108 was examined. Besides pivaloylcarnitine and pivaloylglucuronide, pivaloylglycine was identified in dog urine as a metabolite of pivalic acid by thin-layer chromatography and high-performance liquid chromatography analysis. The concentrations in the plasma of rats to which doses of 6.65, 26.6, and 532 mg/kg of body weight were administered showed dose-proportionate levels. The radioactivity was eliminated rapidly, with a half-life of approximately 3 h until 24 h at both the 6.65- and 26.6-mg/kg doses. Free pivalic acid in plasma accounted for more than 80% of the concentration of radioactivity. Radioactivity was distributed throughout the body and was eliminated quickly at a rate similar to that of radioactivity from plasma. Most of the absorbed radioactivity was excreted in the urine, and it was completed within 24 h after administration. In dogs, the half-life of radioactivity in plasma was longer than that in the rats. The ratio of free pivalic acid in plasma was 60 to 70% of the radioactivity in plasma. The concentration of radioactivity in the liver, cortex of the kidney, and skeletal muscle 144 h after oral dosing was more than 10 times higher than the concentration in plasma for all doses. Urinary excretion in dogs was slower than that in rats. The differences in the disposition of pivalic acid between dogs and rats may account for differences in the degree of skeletal muscle disorders. The safety in humans of S-1108 given at 200 mg three times a day is discussed in relation to the metabolic formation of the carnitine conjugate of pivalic acid and the reduction of the carnitine concentration in plasma. PMID:7492083

  11. Jargonial-Obfuscation(J-O) DISambiguation Elimination via Siegel-Baez Cognition Category-Semantics(C-S) in Siegel FUZZYICS=CATEGORYICS (Son of TRIZ)/(F=C) Tabular List-Format Dichotomy Truth-Table Matrix Analytics

    NASA Astrophysics Data System (ADS)

    Siegel, Carl Ludwig; Siegel, Edward Carl-Ludwig

    2011-03-01

    NOT "philosophy" per se but raising serious salient Arnol'd [Huygens and Barrow, Newton and Hooke(96)] questions begged is Rota empiricism Husserl VS. Frege maths-objects Dichotomy controversy: Hill-Haddock[Husserl or Frege?(00)]as manifestly-demonstrated by Hintikka[B.U.]-Critchey[Derrida Deconstruction Ethics(78)] deconstruction; Altshuler TRIZ; Siegel F=C/C-S; Siegel-Baez(UCR) Cognition C-S = "Category-theory ``+'' Cognitive-Semantics[Wierzbica-Langacker-Lakoff-Nunez[Where Maths Comes From(00)]-Fauconnier-Turner[Blending(98)]-Coulson[Semantic-Leaps (00)

  12. Computational modeling of the bHLH domain of the transcription factor TWIST1 and R118C, S144R and K145E mutants

    PubMed Central

    2012-01-01

    Background Human TWIST1 is a highly conserved member of the regulatory basic helix-loop-helix (bHLH) transcription factors. TWIST1 forms homo- or heterodimers with E-box proteins, such as E2A (isoforms E12 and E47), MYOD and HAND2. Haploinsufficiency germ-line mutations of the twist1 gene in humans are the main cause of Saethre-Chotzen syndrome (SCS), which is characterized by limb abnormalities and premature fusion of cranial sutures. Because of the importance of TWIST1 in the regulation of embryonic development and its relationship with SCS, along with the lack of an experimentally solved 3D structure, we performed comparative modeling for the TWIST1 bHLH region arranged into wild-type homodimers and heterodimers with E47. In addition, three mutations that promote DNA binding failure (R118C, S144R and K145E) were studied on the TWIST1 monomer. We also explored the behavior of the mutant forms in aqueous solution using molecular dynamics (MD) simulations, focusing on the structural changes of the wild-type versus mutant dimers. Results The solvent-accessible surface area of the homodimers was smaller on wild-type dimers, which indicates that the cleft between the monomers remained more open on the mutant homodimers. RMSD and RMSF analyses indicated that mutated dimers presented values that were higher than those for the wild-type dimers. For a more careful investigation, the monomer was subdivided into four regions: basic, helix I, loop and helix II. The basic domain presented a higher flexibility in all of the parameters that were analyzed, and the mutant dimer basic domains presented values that were higher than the wild-type dimers. The essential dynamic analysis also indicated a higher collective motion for the basic domain. Conclusions Our results suggest the mutations studied turned the dimers into more unstable structures with a wider cleft, which may be a reason for the loss of DNA binding capacity observed for in vitro circumstances. PMID:22839202

  13. Microstructural and compositional change of NaOH-activated high calcium fly ash by incorporating Na-aluminate and co-existence of geopolymeric gel and C-S-H(I)

    SciTech Connect

    Oh, Jae Eun; Moon, Juhyuk; Oh, Sang-Gyun; Clark, Simon M.; Monteiro, Paulo J.M.

    2012-05-15

    This study explores the reaction products of alkali-activated Class C fly ash-based aluminosilicate samples by means of high-resolution synchrotron X-ray diffraction (HSXRD), scanning electron microscope (SEM), and compressive strength tests to investigate how the readily available aluminum affects the reaction. Class C fly ash-based aluminosilicate raw materials were prepared by incorporating Na-aluminate into the original fly ashes, then alkali-activated by 10 M NaOH solution. Incorporating Na-aluminate reduced the compressive strength of samples, with the reduction magnitude relatively constant regardless of length of curing period. The HSXRD provides evidence of the co-existence of C-S-H with geopolymeric gels and strongly suggests that the C-S-H formed in the current system is C-S-H(I). The back-scattered electron images suggest that the C-S-H(I) phase exists as small grains in a finely intermixed form with geopolymeric gels. Despite providing extra source of aluminum, adding Na-aluminate to the mixes did not decrease the Si/Al ratio of the geopolymeric gel.

  14. Carbon Storage in the Mid- to Deep- Upper Mantle Constrained by Phase Relations in the Fe-Ni-Cu-C-S system

    NASA Astrophysics Data System (ADS)

    Tsuno, K.; Dasgupta, R.

    2014-12-01

    Carbon is a key element for evolution of terrestrial planets as it has influence on the chemistry and habitability of surficial environment as well as impact on mantle processes such as partial melting and element mobility. Because mantle is arguably the largest reservoir of extractable carbon, the stable form of carbon in various mantle domains needs to be constrained. In the reduced, mid- to deep- upper mantle, the host of deep carbon is graphite/diamond and/or Fe-Ni-bearing alloy melt [1]. However, high solubility of carbon in Fe-Ni alloy melt [2] suggests that diamond saturation may be restricted only to C-rich mantle domains. But such suggestions do not take into account the role of sulfides, which must interact with alloy-carbon mantle subsystems. In order to constrain the stable forms of carbon in the reduced mantle where Ni-rich alloy is likely present [3], we explore the phase relations and C solubility in Ni-rich portion of the Fe-Ni-±Cu-C-S systems. Experiments were performed in a MgO capsule using a multi-anvil with six starting mixes (Ni/(Fe+Ni) wt. ratio of 0.50-0.61, 8-16 % wt.% S, 2.0-2.5 wt.% C, and 0-0.7 wt.% Cu) at 6-8 GPa and 800-1400 °C. Low-temperature runs for all starting mixes contain C-bearing, solid Fe-Ni alloy + alloy melt + graphite, and solid alloy-out boundary is constrained, for example, at 1000-1050 °C at 6 GPa and 900-1000 °C at 8 GPa for the S-rich starting mix. The carbon solubility in the alloy melt (0.8~2.1 wt.% at 8 GPa and 1400 °C) decreases with increasing S content from 8 to 24 wt.%, increasing pressure for S-rich (18-24 wt.%) melt, and decreasing Ni/(Fe+Ni) from 0.65 to 0.53. For a mantle with ~0.1 wt.% alloy (~250 km depth) [3], diamond is likely stable coexisting with an S-rich alloy melt for ≥10 ppm bulk C. This is owing to the influence of S, which suppresses the incorporation of C in the alloy melt to stabilize diamond. Our results thus imply that diamond is a stable form of carbon even in depleted mantle

  15. Calculation of vibrational energy levels of triatomic molecules with the C 2v and C s symmetries by summing divergent series of the Rayleigh-Schrödinger perturbation theory

    NASA Astrophysics Data System (ADS)

    Bykov, A. D.; Kalinin, K. V.

    2012-03-01

    The Rayleigh-Schrödinger perturbation theory is applied to calculation of vibrational energy levels of triatomic molecules with the C 2v and C s symmetries: SO2, H2S, F2O, HOF, HOCl, and DOCl. Particular attention is given to the states coupled by anharmonic resonances; for such states, the perturbation theory series diverge. To sum these series, the known methods of Padé, Padé-Borel, and Padé-Hermite and the method of power moments are used. For low-lying levels, all the summation methods give satisfactory results, while the method of quadratic Padé-Hermite approximants appears to be more efficient for high-excited states. Using these approximants, the structure of singularities of the vibrational energy, as a function in the complex plane, is studied.

  16. Physics Proofs of Four Millennium-Problems(MP) via CATEGORY-SEMANTICS(C-S)/F=C Aristotle SQUARE-of-OPPOSITION(SoO) DEduction-LOGIC DichotomY

    NASA Astrophysics Data System (ADS)

    Clay, London; Siegel, Edward Carl-Ludwig

    2011-03-01

    Siegel-Baez Cognitive-Category-Semantics"(C-C-S) tabular list-format matrix truth-table analytics SoO jargonial-obfuscation elimination query WHAT? yields four "pure"-maths MP "Feet of Clay!!!" proofs: (1) Siegel [AMS Natl.Mtg.(02)-Abs.973-03-126: (CCNY;64)(94;Wiles)] Fermat's: Last-Thm. = Least-Action Ppl.; (2) P=/=NP TRIVIAL simple Euclid geometry/dimensions: NO computer anything"Feet of Clay!!!"; (3) Birch-Swinnerton-Dyer conjecture; (4) Riemann-hypotheses via COMBO.: Siegel[AMS Natl.Mtg.(02)-Abs.973-60-124] digits log-law inversion to ONLY BEQS with ONLY zero-digit BEC, AND Rayleigh[1870;graph-thy."short-CUT method"[Doyle-Snell, Random-Walks & Electric-Nets,MAA(81)]-"Anderson"[(58)] critical-strip C-localization!!! SoO DichotomY ("V") IdentitY: #s:(Euler v Bernoulli) = (Sets v Multisets) = Quantum-Statistics(FD v BE) = Power-Spectra(1/f(0) v 1/f(1)) = Conic-Sections(Ellipse v Hyperbola) = Extent(Locality v Globality);Siegel[(89)] (so MIScalled) "complexity" as UTTER-SIMPLICITY(!!!) v COMPLICATEDNESS MEASURE(S) definition.

  17. Physics Proofs of Four Millennium-Problems(MP) via CATEGORY-SEMANTICS(C-S)/F=C Aristotle SQUARE-of-OPPOSITION(SoO) DEduction-LOGIC DichotomY

    NASA Astrophysics Data System (ADS)

    Clay, L.; Siegel, E.

    2010-03-01

    Siegel-Baez C-S/F=C tabular list-format matrix truth-table analytics SoO jargonial-obfuscation elimination query WHAT? yields four ``pure''-maths MP ``Feet of Clay!!!'' proofs:(1)Siegel [AMS Natl.Mtg.(2002)-Abs.#:973-03-126:(@CCNY;1964!!!)<<<(1994; Wiles)]Fermat's: Last-Theorem = Least-Action Principle; (2) P=/=NP TRIVIAL simple Euclid geometry/dimensions: NO computer anything;``Feet of Clay!!!''; (3)Birch-Swinnerton-Dyer conjecture; (4)Riemann-hypotheses via combination of: Siegel [AMS Natl.Mtg. (2002)-Abs.#:973-60-124 digits logarithmic-law simple algebraic- inversion to ONLY BEQS with ONLY zero-digit BEC, AND Rayleigh [(1870);graph-theory ``short-CUT method''[Doyle- Snell,Random- Walks & Electric-Networks,MAA(1981)]-``Anderson'' [PRL(1958)] critical-strip 1/2 complex-plane localization!!! SoO DichotomY (``v'') IdentitY: numbers(Euler v Bernoulli) = (Sets v Multisets) = Quantum-Statistics(F.-D. v B.-E.) = Power- Spectra(1/f^(0) v 1/f^(1.000...) = Conic-Sections(Ellipse v (Parabola) v Hyperbola) = Extent(Locality v Globality); Siegel [MRS Fractals Symp.(1989)](so MIScalled)``complexity'' as UTTER- SIMPLICITY (!!!) v COMPLICATEDNESS MEASURE(S) definition.

  18. Fe-Ni-Cu-C-S phase relations at high pressures and temperatures - The role of sulfur in carbon storage and diamond stability at mid- to deep-upper mantle

    NASA Astrophysics Data System (ADS)

    Tsuno, Kyusei; Dasgupta, Rajdeep

    2015-02-01

    Constraining the stable form of carbon in the deep mantle is important because carbon has key influence on mantle processes such as partial melting and element mobility, thereby affecting the efficiency of carbon exchange between the endogenic and exogenic reservoirs. In the reduced, mid- to deep-upper mantle, the chief host of deep carbon is expected to be graphite/diamond but in the presence of Fe-Ni alloy melt in the reduced mantle and owing to high solubility of carbon in such alloy phase, diamond may become unstable. To investigate the nature of stable, C-bearing phases in the reduced, mid- to deep-upper mantle, here we have performed experiments to examine the effect of sulfur on the phase relations of the Ni-rich portion of Fe-Ni ± Cu-C-S system, and carbon solubility in the Fe-Ni solid and Fe-Ni-S liquid alloys at 6-8 GPa and 800-1400 °C using a multianvil press. Low-temperature experiments for six starting mixes (Ni/(Fe + Ni) ∼ 0.61, 8-16 wt.% S) contain C-bearing, solid Fe-Ni alloy + Fe-Ni-C-S alloy melt + metastable graphite, and the solid alloy-out boundary is constrained, at 1150-1200 °C at 6 GPa and 900-1000 °C at 8 GPa for S-poor starting mix, and at 1000-1050 °C at 6 GPa and 900-1000 °C at 8 GPa for the S-rich starting mix. The carbon solubility in the liquid alloy significantly diminishes from 2.1 to 0.8 wt.% with sulfur in the melt increasing from 8 to 24 wt.%, irrespective of temperature. We also observed a slight decrease of carbon solubility in the liquid alloy with increasing pressure when alloy liquid contains >∼18 wt.% S, and with decreasing Ni/(Fe + Ni) ratio from 0.65 to ∼0.53. Based on our results, diamond, coexisting with Ni-rich sulfide liquid alloy is expected to be stable in the reduced, alloy-bearing oceanic mantle with C content as low as 20 to 5 ppm for mantle S varying between 100 and 200 ppm. Deep, reduced root of cratonic mantle, on the other hand, is expected to have C distributed among solid alloy, liquid alloy

  19. Two molecular pathways (NMD and ERAD) contribute to a genetic epilepsy associated with the GABA(A) receptor GABRA1 PTC mutation, 975delC, S326fs328X.

    PubMed

    Kang, Jing-Qiong; Shen, Wangzhen; Macdonald, Robert L

    2009-03-01

    Approximately one-third of human genetic diseases are caused by premature translation-termination codon (PTC)-generating mutations. These mutations in sodium channel and GABA(A) receptor genes have been associated with idiopathic generalized epilepsies, but the cellular consequences of the PTCs on the mutant channel subunit biogenesis and function are unknown. The PTCs could result in translation of a truncated subunit, or more likely, trigger mRNA degradation through nonsense-mediated mRNA decay (NMD), thus preventing or reducing production of mutant subunit at the transcriptional level. The GABA(A) receptor alpha1 subunit mutation, 975delC, S326fs328X, is an autosomal dominant mutation associated with childhood absence epilepsy that generates a PTC in exon 8 of the 9 exon GABRA1 gene that is 74 bp upstream of intron 8. Using an intron 8-inclusion minigene that supports NMD, we demonstrated that mutant mRNA was substantially reduced, but not absent. Loss of mutant transcripts was blocked by ribosome inhibition or by silencing the NMD-essential gene hUPF-1. In both neurons and non-neuronal cells, the PTC caused substantial loss of mutant alpha1(S326fs328X) subunit mRNA through NMD with a minor portion of the mRNA escaping NMD and producing a mutant protein. The translated mutant protein had reduced stability due to endoplasmic reticulum associated degradation (ERAD) and had enhanced association with molecular chaperones. This study suggests that loss of mRNA due to activation of NMD and activation of ERAD by the mutant protein may contribute to epileptogenesis. The molecular mechanisms outlined here delineate a model for the pathogenesis of many PTC-generating mutations. PMID:19261879

  20. X-ray crystallographic characterization of new soluble endohedral fullerenes utilizing the popular C82 bucky cage. Isolation and structural characterization of Sm@C3v(7)-C82, Sm@C(s)(6)-C82, and Sm@C2(5)-C82.

    PubMed

    Yang, Hua; Jin, Hongxiao; Wang, Xinqing; Liu, Ziyang; Yu, Meilan; Zhao, Fukun; Mercado, Brandon Q; Olmstead, Marilyn M; Balch, Alan L

    2012-08-29

    Three isomers of Sm@C(82) that are soluble in organic solvents were obtained from the carbon soot produced by vaporization of hollow carbon rods doped with Sm(2)O(3)/graphite powder in an electric arc. These isomers were numbered as Sm@C(82)(I), Sm@C(82)(II), and Sm@C(82)(III) in order of their elution times from HPLC chromatography on a Buckyprep column with toluene as the eluent. The identities of isomers, Sm@C(82)(I) as Sm@C(s)(6)-C(82), Sm@C(82)(II) as Sm@C(3v)(7)-C(82), and Sm@C(82)(III) as Sm@C(2)(5)-C(82), were determined by single-crystal X-ray diffraction on cocrystals formed with Ni(octaethylporphyrin). For endohedral fullerenes like La@C(82), which have three electrons transferred to the cage to produce the M(3+)@(C(82))(3-) electronic distribution, generally only two soluble isomers (e.g., La@C(2v)(9)-C(82) (major) and La@C(s)(6)-C(82) (minor)) are observed. In contrast, with samarium, which generates the M(2+)@(C(82))(2-) electronic distribution, five soluble isomers of Sm@C(82) have been detected, three in this study, the other two in two related prior studies. The structures of the four Sm@C(82) isomers that are currently established are Sm@C(2)(5)-C(82), Sm@C(s)(6)-C(82), Sm@C(3v)(7)-C(82), and Sm@C(2v)(9)-C(82). All of these isomers obey the isolated pentagon rule (IPR) and are sequentially interconvertable through Stone-Wales transformations. PMID:22860880

  1. A,B,C`s of nuclear science

    SciTech Connect

    Noto, V.A.; Norman, E.B.; Chan, Yuen-Dat; Dairiki, J.; Matis, H.S.; McMahan, M.A.; Otto, R.

    1995-08-07

    This introductory level presentation contains information on nuclear structure, radioactivity, alpha decay, beta decay, gamma decay, half-life, nuclear reactions, fusion, fission, cosmic rays, and radiation protection. Nine experiments with procedures and test questions are included.

  2. D.C.'s Chancellor Makes Her Case

    ERIC Educational Resources Information Center

    Maxwell, Lesli A.

    2008-01-01

    Michelle A. Rhee, the chancellor of the public schools in Washington D.C. since June 2007, has become a favorite of the school reform set due to her bold efforts to remake the public schools in the nation's capital. For Rhee, exposing mismanagement, incompetence, and wide disparities in teaching quality has been a deliberate tactic as she builds…

  3. Special catalyst improves c-s compounds conversion

    SciTech Connect

    Pearson, M.J.

    1981-04-01

    Carbon-sulfur compounds normally formed in the Claus furnace can be almost totally decomposed when a promoted catalyst is used rather than a standard unpromoted catalyst. Compound formation and decomposition chemistries are described. The use of a promoted active alumina is shown to yield better results compared with a standard active alumina catalyst.

  4. Hemoglobin C, S-C, and E Diseases

    MedlinePlus

    ... Drug Information, Search Drug Names, Generic and Brand Natural Products, Search Drug Interactions Pill Identifier News & Commentary ALL NEWS > Resources First Aid Videos Figures Images Audio Pronunciations The ...

  5. Unexpected reactions of 2,5-dimethylthiopene (2,5-Me{sub 2}t) in Cp{sup *}Ir({eta}{sup 5}-2,5-Me{sub 2}T){sup 2+}, Cp{sup *}Ir({eta}{sup 4}-2,5-Me{sub 2}T), and Cp{sup *}Ir(C,S-2,5-Me{sub 2}T) with cobaltocene

    SciTech Connect

    Chen, J.; Daniels, L.M.; Angelica, R.J. |

    1996-02-20

    The reaction of Cp{sup *}Ir({eta}{sup 5}-2,5-Me{sub 2}T){sup 2+} (1) (Cp{sup *} = {eta}{sup 5}-C{sub 5}Me{sub 5}) with the reducing agent Cp{sub 2}Co yields Cp{sup *}Ir({eta}{sup 4}-2,5-Me{sub 2}T) (2) and Cp{sup *}Ir(C,S-2,5-Me{sub 2}T) (3), as well as the unexpected Cp{sup *}Ir({eta}{sup 4}-2,5-Me{sub 2}T{center_dot}C{sub 5}H{sub 4}) (4), which can also be prepared by reacting 1 with Cp{sup -}. An X-ray diffraction study of 4 shows the {eta}{sup 4}-2,5-Me{sub 2}T{center_dot}C{sub 5}H{sub 5} ligand to be a ring-opened 2,5-Me{sub 2}T allyl thiolate conjugated to a cyclopentadienylidene unit. The reduced products 2 and 3 react with Cp{sub 2}Co to give a ferrole-type product Cp{sup *}[IrC(Me)=CHCH=C(Me)]CoCp in which the planar iridacyclopentadiene ring is {pi}-bonded to the cobalt, as established by a structural investigation. The Cp{sup *}Co analog of 5 is prepared by the reaction of 2 or 3 with Cp{sup *}Co(CH{sub 2}=CH{sub 2}){sub 2}. These studies demonstrate that cobaltocene and Cp{sup *}Co(CH{sub 2}=CH{sub 2}){sub 2} readily desulfurize the 2,5-dimethylthiophene ligand in 2 and 3, which supports a previously proposed mechanism for the thiophene hydrodesulfurization. 37 refs., 2 figs., 5 tabs.

  6. Portal vein thrombosis with protein C-S deficiency in a non-cirrhotic patient

    PubMed Central

    Rodríguez-Leal, Gustavo A; Morán, Segundo; Corona-Cedillo, Roberto; Brom-Valladares, Rocío

    2014-01-01

    There are several conditions that can lead to portal vein thrombosis (PVT), including including infection, malignancies, and coagulation disorders. Anew condition of interest is protein C and S deficiencies, associated with hypercoagulation and recurrent venous thromboembolism. We report the case of a non-cirrhotic 63-year-old male diagnosed with acute superior mesenteric vein thrombosis and PVT and combined deficiencies in proteins C and S, recanalized by short-term low molecular heparin plus oral warfarin therapy. PMID:25068006

  7. The F. C. C.'s Clear Channel Radio Policies: Regulation in the Slow Lane.

    ERIC Educational Resources Information Center

    Jassem, Harvey C.

    In 1928, the Federal Radio Commission (the precursor of the Federal Communications Commission--FCC) noted the need for special radio channels that could carry radio across the United States free from interference from other radio stations. Many of these "clear channels" still exist as protected entities. Perhaps no other FCC policy better reflects…

  8. Role of TBATB in nano indium oxide catalyzed C-S bond formation

    PubMed Central

    Gogoi, Prasanta; Hazarika, Sukanya; Barman, Pranjit

    2015-01-01

    Nano sized indium oxide is found to be an efficient catalyst for the conversion of thiols to sulfides using Na2CO3 as base and TBATB as reagent in DMSO at 110 °C. Here in situ generation of bromo intermediate by TBATB takes place through indium surface. A variety of aryl sulfides can be synthesized in excellent yields from less reactive chlorides, boronic acids and thiols. PMID:26415729

  9. Success in College: From "C"s in High School to "A"s in College

    ERIC Educational Resources Information Center

    Burns, Peter F.

    2006-01-01

    This book provides important information and advice that students need in order to learn more and receive higher grades offers strategies for test and note taking, studying, writing papers, and making class schedules. This book also gives an insider's guide to the academic semester, in-class behavior, and how and when to approach professors.…

  10. {sup 15}N(p,{alpha}{sub 0}){sup 12}C S factor

    SciTech Connect

    Barker, F. C.

    2008-10-15

    Experimental values of the astrophysical S factor for the {sup 15}N(p,{alpha}{sub 0}){sup 12}C reaction are available both from direct measurements and from the Trojan horse method. We here use R-matrix formulas to fit these values and to extrapolate to zero energy to obtain values of S(0)

  11. Creep of a C-S-H gel: a micromechanical approach.

    PubMed

    Sanahuja, Julien; Dormieux, Luc

    2010-03-01

    Both clays and calcium silicate hydrates(the main hydration products of Portland cements) exhibit a microstructure made up of lamellar particles. The microscopic mechanism responsible for the macroscopic creep of such materials is often described as the relative sliding of the sheets. This paper proposes a micromechanical approach to estimate the macroscopic creep behavior rising from this microscopic mechanism. The asymptotic evolution of creep at both short- and long-term is especially investigated. More precisely, a non-vanishing initial elastic strain is retrieved. At long-term, a threshold on porosity appears. At lower porosities, the creep evolution admits an asymptotic strain. At higher porosities, it admits an asymptotic strain rate. PMID:20209241

  12. D.C.'s Achievement Gap: Why Place Matters. Data Snapshot

    ERIC Educational Resources Information Center

    DC Action for Children, 2012

    2012-01-01

    Every child deserves educational opportunity and the chance to achieve, no matter his or her school, neighborhood or background. Unfortunately, large and persistent disparities in achievement among public school students in the District of Columbia indicate that all children here may not have the same opportunities. This Data Snapshot examines…

  13. New Leaders for Troubled Schools: Jacquelyn Davis Works with D.C.'s Education Bureaucracy

    ERIC Educational Resources Information Center

    Currie, Tyler

    2007-01-01

    In this article the author presents Jacquelyn Davis, the executive director of the Washington office of New Leaders for New Schools (NLNS), a nonprofit dedicated to training recruits drawn from a range of sectors for leadership in failing school systems. Davis is overseeing a rapidly expanding crop of new principals who are promising to revitalize…

  14. Biostimulation induces syntrophic interactions that impact C, S and N cycling in a sediment microbial community

    SciTech Connect

    Handley, KM; Verberkmoes, Nathan C; Steefel, Carl I; Sharon, I; Williams, Ken; Miller, CS; Frischkorn, Kyle C; Chourey, Karuna; Thomas, Brian; Shah, Manesh B; Long, Phil; Hettich, Robert {Bob} L; Banfield, Jillian F.

    2013-01-01

    Stimulation of subsurface microorganisms to induce reductive immobilization of metals is a promising approach for bioremediation, yet the overall microbial community response is typically poorly understood. Here we used community proteogenomics to test the hypothesis that excess input of acetate activates syntrophic interactions among autotrophs and heterotrophs. A flow-through sediment column was incubated in a groundwater well of an acetate-amended aquifer. Genomic sequences from the community recovered during microbial sulfate reduction were used to econstruct, de novo, near-complete genomes for Desulfobacter (Deltaproteobacteria) and relatives of Sulfurovum and Sulfurimonas (Epsilonproteobacteria), and Bacteroidetes. Partial genomes were obtained for Clostridiales (Firmicutes) and Desulfuromonadales-like Deltaproteobacteria. The majority of proteins identified by mass spectrometry corresponded to Desulfobacter-like species, and demonstrate the role of this organism in sulfate reduction (Dsr and APS), nitrogen-fixation (Nif) and acetate oxidation to CO2 during amendment. Results suggest less abundant Desulfuromonadales and Bacteroidetes also actively contributed to CO2 production via the TCA cycle. Proteomic data indicate that sulfide was partially re-oxidized by Epsilonproteobacteria through nitrate-dependent sulfide oxidation (using Nap, Nir, Nos, SQR and Sox), with CO2 fixed using the reverse TCA cycle. Modeling shows that this reaction was thermodynamically possible, and kinetically favorable relative to acetate-dependent denitrification. We conclude that high-levels of carbon amendment aimed to stimulate anaerobic heterotrophy led to carbon fixation in co-dependent chemoautotrophs. These results have implications for understanding complex ecosystem behavior, and show that high levels of organic carbon supplementation can expand the range of microbial functionalities accessible for ecosystem manipulation.

  15. Social Studies in the Nineties: An N.H.C.S.S. Statement.

    ERIC Educational Resources Information Center

    Adams, Ron; And Others

    The goal of the New Hampshire Council for the Social Studies is to actively work to improve social studies instruction in New Hampshire in the 1990s. This guide outlines the basic goals, structure, and methods of the social studies curriculum, K-12, for New Hampshire. The guide provides a definition along with a rationale for social studies…

  16. Global nuclear material monitoring with NDA and C/S data through integrated facility monitoring

    SciTech Connect

    Howell, J.A.; Menlove, H.O.; Argo, P.; Goulding, C.; Klosterbuer, S.; Halbig, J.

    1996-09-01

    This paper focuses on a flexible, integrated demonstration of a monitoring approach for nuclear material monitoring. This includes aspects of item signature identification, perimeter portal monitoring, advanced data analysis, and communication as a part of an unattended continuous monitoring system in an operating nuclear facility. Advanced analysis is applied to the integrated nondestructive assay and containment and surveillance data that are synchronized in time. End result will be the foundation for a cost-effective monitoring system that could provide the necessary transparency even in areas that are denied to foreign nationals of both US and Russia should these processes and materials come under full-scope safeguards or bilateral agreements. Monitoring systems of this kind have the potential to provide additional benefits including improved nuclear facility security and safeguards and lower personnel radiation exposures. Demonstration facilities in this paper include VTRAP-prototype, Los Alamos Critical Assemblies Facility, Kazakhstan BM-350 Reactor monitor, DUPIC radiation monitoring, and JOYO and MONJU radiation monitoring.

  17. A Multicultural Social Studies Series for C.S.L. Students. Book 1. Europe.

    ERIC Educational Resources Information Center

    Chan, Yiu Man

    This text is written primarily for students of Chinese as a second language who are continuing in the ESEA Title VII Chinese Bilingual Pilot Program at the secondary level, and introduces different aspects and general knowledge of Europe. The text is divided into twenty-five lessons, having the following headings: European Countries, Class, On the…

  18. Late-Type Stars in M31. II. C-, S-, and M-Star Spectra

    NASA Astrophysics Data System (ADS)

    Brewer, James P.; Richer, Harvey B.; Crabtree, Dennis R.

    1996-08-01

    We present spectra of AGB stars in M31 for which observations had been previously secured using a four-band photometric system (FBPS). The FBPS had been used to identify M-, S-, and carbon-star (C-star) candidates, and we use the spectra to show that the FBPS did an excellent job at identifying C- and M-stars. Of the 48 C-stars for which spectra were obtained, 7 have strongly enhanced ^13^C bands (J-stars), 2 have strong Hα emission, while 3 are found to exhibit enhanced Li absorption (Li-stars). Both the J- and Li-stars are fainter than predicted by current theoretical models, while the colors of the Hα stars suggest they may be in the terminal phases of their evolution. The C_2_ and CN bandstrengths of the C-stars are measured, and no correlation between these bandstrengths and either M_bol_ or (V-I) is found. It is suggested that this lack of correlation is due to an age spread. The spectra of the first confirmed S-star in M31 is presented, and two evolutionary pathways are suggested to account for this star's high luminosity.

  19. A Multicultural Social Studies Series for C.S.L. Students, Book 2.

    ERIC Educational Resources Information Center

    Moy, Mary C.; And Others

    A multicultural social studies text for junior high school students of Chinese as a second language is presented. This level two text is designed for the Chinese Bilingual Pilot Program sponsored through the Elementary and Secondary Education Act, Title VII. The book consists of 25 lessons with no more than 50 characters each. Each lesson has a…

  20. Biostimulation induces syntrophic interactions that impact C, S and N cycling in a sediment microbial community

    PubMed Central

    Handley, Kim M; VerBerkmoes, Nathan C; Steefel, Carl I; Williams, Kenneth H; Sharon, Itai; Miller, Christopher S; Frischkorn, Kyle R; Chourey, Karuna; Thomas, Brian C; Shah, Manesh B; Long, Philip E; Hettich, Robert L; Banfield, Jillian F

    2013-01-01

    Stimulation of subsurface microorganisms to induce reductive immobilization of metals is a promising approach for bioremediation, yet the overall microbial community response is typically poorly understood. Here we used proteogenomics to test the hypothesis that excess input of acetate activates complex community functioning and syntrophic interactions among autotrophs and heterotrophs. A flow-through sediment column was incubated in a groundwater well of an acetate-amended aquifer and recovered during microbial sulfate reduction. De novo reconstruction of community sequences yielded near-complete genomes of Desulfobacter (Deltaproteobacteria), Sulfurovum- and Sulfurimonas-like Epsilonproteobacteria and Bacteroidetes. Partial genomes were obtained for Clostridiales (Firmicutes) and Desulfuromonadales-like Deltaproteobacteria. The majority of proteins identified by mass spectrometry corresponded to Desulfobacter-like species, and demonstrate the role of this organism in sulfate reduction (Dsr and APS), nitrogen fixation and acetate oxidation to CO2 during amendment. Results indicate less abundant Desulfuromonadales, and possibly Bacteroidetes, also actively contributed to CO2 production via the tricarboxylic acid (TCA) cycle. Proteomic data indicate that sulfide was partially re-oxidized by Epsilonproteobacteria through nitrate-dependent sulfide oxidation (using Nap, Nir, Nos, SQR and Sox), with CO2 fixed using the reverse TCA cycle. We infer that high acetate concentrations, aimed at stimulating anaerobic heterotrophy, led to the co-enrichment of, and carbon fixation in Epsilonproteobacteria. Results give an insight into ecosystem behavior following addition of simple organic carbon to the subsurface, and demonstrate a range of biological processes and community interactions were stimulated. PMID:23190730

  1. Homolytic S-S bond dissociation of 11 bis(thiocarbonyl)disulfides R-C(=S)-S-S-C(=S)R and prediction of a novel rubber vulcanization accelerator.

    PubMed

    Mak, Adrian Matthew; Steudel, Ralf; Wong, Ming Wah

    2008-06-01

    The structures and energetics of eight substituted bis(thiocarbonyl)disulfides (RCS(2))(2), their associated radicals RCS(2)(*), and their coordination compounds with a lithium cation have been studied at the G3X(MP2) level of theory for R = H, Me, F, Cl, OMe, SMe, NMe(2), and PMe(2). The effects of substituents on the dissociation of (RCS(2))(2) to RCS(2)(*) were analyzed using isodesmic stabilization reactions. Electron-donating groups with an unshared pair of electrons have a pronounced stabilization effect on both (RCS(2))(2) and RCS(2)(*). The S-S bond dissociation enthalpy of tetramethylthiuram disulfide (TMTD, R = NMe(2)) is the lowest in the above series (155 kJ mol(-1)), attributed to the particular stability of the formed Me(2)NCS(2)(*) radical. Both (RCS(2))(2) and the fragmented radicals RCS(2)(*) form stable chelate complexes with a Li(+) cation. The S-S homolytic bond cleavage in (RCS(2))(2) is facilitated by the reaction [Li(RCS(2))(2)](+)+Li(+)-->2 [Li(RCS(2))](*+). Three other substituted bis(thiocarbonyl) disulfides with the unconventional substituents R = OSF(5), Gu(1), and Gu(2) have been explored to find suitable alternative rubber vulcanization accelerators. Bis(thiocarbonyl)disulfide with a guanidine-type substituent, (Gu(1)CS(2))(2), is predicted to be an effective accelerator in sulfur vulcanization of rubber. Compared to TMTD, (Gu(1)CS(2))(2) is calculated to have a lower bond dissociation enthalpy and smaller associated barrier for the S-S homolysis. PMID:18418826

  2. Heterogeneous Decomposition of Volatile Organic Compounds by Visible-Light Activated N, C, S-Embedded Titania.

    PubMed

    Chun, Ho-Hwan; Jo, Wan-Kuen

    2016-05-01

    In this study, a N-, C-, and S-doped titania (NCS-TiO2) composite was prepared by combining the titanium precursor with a single dopant source, and the photocatalytic activity of this system for the decomposition of volatile organic compounds (VOCs) at indoor-concentration levels, under exposure to visible light, was examined. The NCS-TiO2 composite and the pure TiO2 photocatalyst, used as a reference, were characterized via X-ray diffraction, scanning electron microscopy, ultraviolet-visible diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy, and Fourier transform infrared spectroscopy. The average efficiencies of benzene, toluene, ethyl benzene, and o-xylene decomposition using NCS-TiO2 for were 70, 87, -100, and -100%, respectively, whereas the values obtained using the pure TiO2 powder were -0, 18, 49, and 51%, respectively. These results suggested that, for the photocatalytic decomposition of toxic VOCs under visible-light exposure conditions, NCS-TiO2 was superior to the reference photocatalyst. The decomposition efficiencies of the target VOCs were inversely related to the initial concentration and relative humidity as well as to the air-flow rate. The decomposition efficiencies of the target chemicals achieved with a conventional lamp/NCS-TiO2 system were higher than those achieved with a light emitting diode/NCS-TiO2 system. Overall, NCS-TiO2 can be used for the efficient decomposition of VOCs under visible-light exposure, if the operational conditions are optimized. PMID:27483788

  3. Reid's Read-Alouds 2: Modern-Day Classics from C.S. Lewis to Lemony Snicket

    ERIC Educational Resources Information Center

    Reid, Rob

    2011-01-01

    Need a one-stop resource for jumpstarting sleepy library visitors? Ready to add punch to classroom discussions? In this companion to his best-selling book "Reid's Read-Alouds", children's lit guru Reid dips back into the classics to highlight outstanding titles published between 1950 and 1999 that continue to connect with kids and teens today.…

  4. The Career Information Center Handbook. A Guide for Developing C.I.C.'s in Local Schools.

    ERIC Educational Resources Information Center

    Holiman, Marjorie A., Ed.; And Others

    The Career Information Center (CIC) handbook is designed to serve as a reference work or blueprint containing a rationale and specific how-to suggestions to support and guide the user's development of a CIC that fits local needs. The format of the handbook is intended to indicate the major steps in the planning, development, and operation of a…

  5. Hydrographic variability in Bahia De La Paz, B. C. S, Mexico, during the 1997 1998 El Niño

    NASA Astrophysics Data System (ADS)

    Obeso-Nieblas, M.; Shirasago, B.; Sánchez-Velasco, L.; Gaviño-Rodriguez, J. H.

    2004-03-01

    Bahı´a de La Paz is an integral part of the coast of the Gulf of California and is the biggest bay of the eastern side of the Baja California Peninsula. Dynamic forcing and water interchange occur between the bay and the gulf through two different openings, the main and deep North Mouth with 350-m depth and the shallow San Lorenzo Channel with an average depth of 10 m. To determine the oceanographic conditions before and during El Niño 1997-1998 in Bahia de La Paz, CTD data were collected in four surveys aboard the research yacht CICIMAR XV during July 1996, March 1997, July 1997, and March 1998. The results revealed important variations in the hydrographic structure of the bay, both in space and time. The two summers had a complete absence of the mixed layer with a sharper thermocline during summer 1996 (0.25°C/m) than in summer 1997 (0.21°C/m). Additionally, the entire water column experienced an average temperature increase from 1.5°C at the surface with a maximum of 4.2°C to 28 m and around 1°C between 100 and 350 m, showing a halocline structure in summer 1997. At the end of the winters of 1997 and 1998, a 50-m mixed layer was detected, with higher average temperatures of 2.3°C in winter 1998. The temperature differences decreased with depth and were the same at 340 m with no traces of the halocline in winter 1998. The increase of temperature observed in the study area during the periods affected by El Niño 1997-1998 resulted in a sinking of the thermocline and isotherms, showing the strongest effect of this warming (>4°C) in the surface layer to 70 m during summer 1997. The stratification increased during the El Niño and was more evident in the period of small stratification in the region (winter) as showed by the φ parameter with values of 45 J/m3 in 1998 and 29 J/m3 in 1997, whereas during the strong stratification period (summer) the difference was small, with values of 137 J/m3 in 1996 and 139 J/m3 in 1997. In periods not affected by El Niño, the Gulf of California and the Subtropical Subsurface Waters are usually present in the bay, but during this episode their presence varies in space. Additionally, Surface Equatorial Water was found in the bay, mainly at the end of winter 1998 and with some traces in summer 1997.

  6. An Analysis of Qualities of Self-Directedness as Related to Selected Characteristics of I.S.C.S. Students

    ERIC Educational Resources Information Center

    McCurdy, D. W.

    1975-01-01

    Reports a study to assess the relationship between student self ratings on ten variables considered skills of self-direction and (1) success in the course, (2) level of the student in the Intermediate Science Curriculum Study program, (3) school where the student attended, and (4) sex of the student. (GS)

  7. An Analysis of Qualities of Self-Directedness as Related to Selected Characteristics of I.S.C.S. Students.

    ERIC Educational Resources Information Center

    McCurdy, Donald W.

    This research project provides an individualized format for a three-year integrated junior high school science curriculum. The purpose of the study was to assess the relationship between student self-ratings on such variables as (1) ability to operate independently of the teacher, (2) use class time effectively, (3) develop their own plan for…

  8. Challenging the Objectivist Paradigm: Teaching Biblical Theology with J. R. R. Tolkien, C. S. Lewis, and Guillermo del Toro

    ERIC Educational Resources Information Center

    Lief, Jason

    2009-01-01

    The dissimilarity that exists between the historical and cultural situation of North American college students and the world described by the biblical authors poses a problem for theological and religious education. While the biblical authors tell fantastic stories of miracle and magic, the scientific and technological paradigm prevalent in…

  9. Hydrodynamical description of 200{bold {ital A}} GeV/{ital c} S+Au collisions: Hadron and electromagnetic spectra

    SciTech Connect

    Sollfrank, J.; Huovinen, P.; Kataja, M.; Ruuskanen, P.V.; Prakash, M.; Venugopalan, R.

    1997-01-01

    We study relativistic S+Au collisions at 200A GeV/c using a hydrodynamical approach. We test various equations of state (EOS{close_quote}s), which are used to describe the strongly interacting matter at densities attainable in the CERN-SPS heavy ion experiments. For each EOS, suitable initial conditions can be determined to reproduce the experimental hadron spectra; this emphasizes the ambiguity between the initial conditions and the EOS in such an approach. Simultaneously, we calculate the resulting thermal photon and dielectron spectra, and compare with experiments. If one allows the excitation of resonance states with increasing temperature, the electromagnetic signals from scenarios with and without phase transition are very similar and are not resolvable within the current experimental resolution. Only EOS{close_quote}s with a few degrees of freedom up to very high temperatures can be ruled out presently. We deduce an upper bound of about 250 MeV for the initial temperature from the single photon spectra of WA80. With regard to the CERES dilepton data, none of the EOS{close_quote}s considered, in conjunction with the standard leading order dilepton rates, succeed in reproducing the observed excess of dileptons below the {rho} peak. Our work, however, suggests that an improved measurement of the photon and dilepton spectra has the potential to strongly constrain the EOS. {copyright} {ital 1997} {ital The American Physical Society}

  10. Insight into elastic behavior of calcium silicate hydrated oxide (C-S-H) under pressure and composition effect

    SciTech Connect

    Zaoui, Ali

    2012-02-15

    The present work relates to the study of structural and elastic properties of Tobermorite 11 A as a function of external pressure and composition in terms of calcium to silicon ratio. Basing on the lattice dynamics method, the main aim of this work is precisely to shed light, for the first time, on the high pressure structural phase transition in Tobermorite 11 A and the possible correlation with some elastic quantities. In order to check the transferability of the potentials used we have, additionally, performed a single calculation based on the density functional theory (DFT) for a pressure of 15 GPa in the case of Ca/Si = 1. The variation of the unit cell parameters with pressure indicates that Tobermorite 11 A undergoes a structural instability around 15 GPa along b-axis and around 20 GPa along a-axis which is confirmed from our calculations of X-Rays diffraction patterns at various pressure values. We have also observed the anisotropic character of the Tobermorite structure for both cases (Ca/Si = 1 and Ca/Si = 0.83). Our results show that around 20 GPa an important change appears in the elastic behaviour of Tobermorite. As pressure increases the calculated elastic quantities for Ca/Si = 1 became closer to those evaluated for Ca/Si = 0.83, which may stimulate further experimental and theoretical research on the matter.

  11. Hydrogen Induced C-C, C-N, & C-S Bond Activation on Pt & Ni Surfaces

    SciTech Connect

    Gland, J. L.

    2004-07-29

    The primary reactions investigated were chosen based on their importance in fuel and chemical production as well as in environmental remediation, and include reactions for hydrodesulfurization (HDS), hydrodenitrogenation (HDN), carbon-carbon hydrogenolysis, and hydrocarbon oxidation.

  12. [Hydrogen induced C-C, C-N, and C-S bond activities on Pi and Ni surfaces]: Summary

    SciTech Connect

    Gland, J.L.

    1994-12-31

    This document summarizes research applied to chemical bond activation studies. Topics summarized include: Carbon nitrogen bonds experimentation with aniline on Ni(111), Mi(100), and Pt(111) surfaces; carbon sulfur bonds experimentation with methanethiol, phenylthiol, and dimethyl disulfide on Pt(111) and Ni(111) surfaces; carbon-carbon bonds experimentation on Ni(100), Ni(111) and Pt(111) surfaces; and in-situ fluorescence yield near edge spectroscopy.

  13. Chemical model for cement-based materials: Thermodynamic data assessment for phases other than C-S-H

    SciTech Connect

    Blanc, Ph.; Bourbon, X.; Lassin, A.; Gaucher, E.C.

    2010-09-15

    In the context of waste confinement, concrete may be used both as a confinement and as a building material. Concerning radwaste, the heat released during radioactive decay will modify the equilibrium constants of the minerals forming the concrete. The present work aims to elucidate the temperature dependency of the thermodynamic functions related to minerals from the concrete or associated with some of its degradation products. A large set of experimental data has been collected, for the chemical systems SO{sub 3}-Al{sub 2}O{sub 3}-CaO-CO{sub 2}-Cl-H{sub 2}O and SiO{sub 2}-Al{sub 2}O{sub 3}-CaO-H{sub 2}O, including iron and magnesium bearing phases. Most of the data collected concern experiments in aqueous media but results from calorimetric studies were also included, when available. Based on selected thermodynamic properties for each phase, predominance diagrams were drawn for the chemical elements listed above. Phase relations reported into predominance diagram appear rather consistent with most of the literature results. The case of katoite has been especially discussed, because it shows inconsistencies with respect to a hydrogarnet-grossular solid solution and with respect to phase relations reported into already published works. Finally, we underline the chemical compatibility of Portland cement pastes with carbonate aggregates, compared to silicates, for long-term storage applications.

  14. Simultaneous N, C, S isotopic analyses using purge and trap EA technology. Application to δ34S analyses of natural phosphate material NBS120c and BCR32

    NASA Astrophysics Data System (ADS)

    Fourel, F. P.; Lecuyer, C.; Martineau, F.

    2013-12-01

    The first example of stable isotope analyses in continuous flow mode by Preston et al in 19861 involved Elemental Analyser Isotopic Ratio Mass Spectrometry (EA-IRMS) dedicated to carbon isotopes in combustion mode. EA-IRMS has since then evolved to allow 34S/32S determinations still in combustion mode and mainly to access pyrolysis reaction for O and H isotopes. As far as combustion EA-IRMS is concerned the technique itself has remained unchanged since the development of 'purge and trap' separation techniques online with IRMS instruments. Here we have used a high-precision, easy, low-cost and rapid method of simultaneous carbon, nitrogen and sulphur isotope analysis using this new type of elemental analyser based on 'purge and trap' technology 2,3. Simultaneous determinations, performed on the same aliquot of 13C, 15N and 34S are demonstrated. Emphasis is put on the high quality of 34S/32S determinations. First concentrating on peak shapes, yields of conversion and preliminary results. Then the reliability and accuracy of such a technique is illustrated using analyses from various international reference materials. Alongside international reference material working NCS calibrated material has been selected and characterized prior to apply this technology to calibrate natural phosphate material used as compositional reference material BCR32 and NBS120c. δ34S values of respectively 15.62×0.32‰ and 16.5×0.17‰ are proposed for those samples with sulphur concentrations below the 1% level. The possibility to reliably measure S isotopes on that kind of samples opens up new fields of investigation especially for paleoenvironmental reconstructions. Keywords: carbon, nitrogen, sulfur, isotope, combustion, phosphate, elemental-analyser 1. T. Preston, N.J.P. Owens: Preliminary 13C Measurements using a Gas Chromatograph Interfaced to an Isotope Ratio Mass Spectrometer. Biomedical. Mass Spectrom. 1985, 12-9, 510. 2. H.P. Sieper, H.J. Kupka, L. Lange, A. Rossmann, N. Tanz , H.L. Schmidt. Essential methodological improvements in the oxygen isotope ratio analysis of N-containing organic compounds Rapid Commun. Mass Spectrom. 2010, 24, 2849. 3. F. Fourel, F.Martineau, C. Lecuyer, H.J. Kupka, L. Lange, C. Ojeimi and M. Seed. 18O/16O ratio measurements of inorganic and organic materials by EA-Pyrolysis-IRMS continuous flow techniques. 2011, Rapid Commun.Mass Spectrom. 2011, 25, 2691.

  15. The C-S Lyases of Higher Plants : Direct Comparison of the Physical Properties of Homogeneous Alliin Lyase of Garlic (Allium sativum) and Onion (Allium cepa).

    PubMed

    Nock, L P; Mazelis, M

    1987-12-01

    Garlic and onion alliin lyases, although from closely related species, have many differences. The two enzymes differ in their K(m) values, pH optima, and isoelectric points. There is a major difference in their molecular weight and subunit structure. The garlic holoenzyme has a molecular weight of 85,000 and consists of two subunits of molecular weight 42,000. The onion enzyme has a holoenzyme molecular weight of 200,000 composed of four subunits of molecular weight 50,000. The onion enzyme is much more difficult to dissociate into its subunits which suggests differences in subunit interaction between the two enzymes. The dimeric stucture of the garlic and the tetrameric structure of the onion enzyme is consistent with a coenzyme content (pyridoxal-5'-phosphate) equivalent to one mole per subunit. The two enzymes vary vastly in their spectra, the onion enzyme having a lower pyridoxal-5'-phosphate absorbance at 430 nanomoles and an inability to react with l-cysteine. Both enzymes are glycoproteins and bind to concanavalin A-Sepharose columns. The onion alliin lyase binds more tightly than the garlic enzyme. The amino acid content of both enzymes is similar as is the carbohydrate content. However, upon hydrolysis the onion lyase does yield more mannose units than the garlic enzyme which is consistent with the former's stronger affinity for concanavalin A. PMID:16665807

  16. Effect of three cooking methods on nutrient components and antioxidant capacities of bamboo shoot (Phyllostachys praecox C.D. Chu et C.S. Chao)*

    PubMed Central

    Zhang, Jin-jie; Ji, Rong; Hu, Ya-qin; Chen, Jian-chu; Ye, Xing-qian

    2011-01-01

    Three cooking methods, namely boiling, steaming, and stir-frying for 5 to 10 min, were used to evaluate the effect on nutrient components, free amino acids, L-ascorbic acid, total phenolic contents, and antioxidant capacities of bamboo shoots (Phyllostachys praecox). Results showed that boiling and stir-frying had a great effect on the nutrient components and they decreased the contents of protein, soluble sugar, and ash, and caused a great loss in the total free amino acids (decreased by 38.35% and 34.86%, respectively). Significant differences (P<0.05) in free amino acids were observed in the samples cooked by different methods. Stir-fried bamboo shoots had a high fat content which increased by 528.57% because of the addition of edible oil. After boiling, the L-ascorbic acid and total phenolic contents were significantly reduced, while steaming increased total phenolic content by 3.98% and stir-frying well-preserved L-ascorbic acid (78.87% of its previous content). Results of the antioxidative property study showed that stir-frying could increase antioxidant capacities of bamboo shoots. It is concluded that stir-frying is more suitable for bamboo shoots because it could obtain the maximum retention of antioxidant capacities. PMID:21887851

  17. Recognition of a novel type X═N-Hal···Hal (X = C, S, P; Hal = F, Cl, Br, I) halogen bonding.

    PubMed

    Gushchin, Pavel V; Kuznetsov, Maxim L; Haukka, Matti; Kukushkin, Vadim Yu

    2013-04-01

    The chlorination of the eight-membered platinum(II) chelates [PtCl2{NH═C(NR2)N(Ph)C(═NH)N(Ph)C(NR2)═NH}] (R = Me (1); R2 = (CH2)5 (2)) with uncomplexed imino group with Cl2 gives complexes bearing the ═N-Cl moiety [PtCl4{NH═C(NR2)N(Ph)C(═NCl)N(Ph)C(NR2)═NH}] (R = Me (3); R2 = (CH2)5 (4)). X-ray study for 3 revealed a novel type intermolecular halogen bonding ═N-Cl···Cl(-), formed between the Cl atom of the chlorinated imine and the chloride bound to the platinum(IV) center. The processing relevant structural data retrieved from the Cambridge Structural Database (CSDB) shows that this type of halogen bonding is realized in 18 more molecular species having X═N-Hal moieties (X = C, P, S, V, W; Hal = Cl, Br, I), but this weak ═N-Hal···Hal(-) bonding was totally neglected in the previous works. The presence of the halogen bonding in 3 was confirmed by theoretical calculations at the density functional theory (DFT, M06-2X) level, and its nature was analyzed. PMID:23469756

  18. Determination of acidic sulfate aerosols in urban atmospheres in Erfurt (F.R.G.) and Sokolov (Former C.S.S.R.)

    NASA Astrophysics Data System (ADS)

    Cyrys, J.; Gutschmidt, K.; Brauer, M.; Dumyahn, T.; Heinrich, J.; Spengler, J. D.; Wichmann, H. E.

    Acidic sulfate aerosols were sampled from the atmosphere with the Harvard Impactor-Honeycomb Denuder System. This sampler incorporates a citric-acid-coated denuder to remove NH 3 and an impactor with a 50% size cutoff of 2.5 μm ( da). Fine particles were collected on a Teflon filter. The sampling (24 h) lasted from December 1990 until June 1992. The sampling sites were in Erfurt and Sokolov, two eastern European cities with high SO 2 concentrations. At the same time approximately 230 asthmatic children and adults were followed by daily peak flow measurements and symptom diaries. Despite the high SO 2 pollution with daily averages of 62 μg m -3 and peaks of nearly 500 jug m -3, the mean SO 4-2 concentration for Erfurt, 9.8 μg m -3, and that for Sokolov, 8.9 μg m -3, were moderate. In addition, the average H + concentration over the entire period was low in Erfurt (0.3 μg m -3, H + as H 2SO 4) as well as in Sokolov (0.4 μg m -3). H + concentrations tended, however, to be higher during the cold winter months and the hot summer months. In Sokolov, there were three episodes in the winter when measurements exceeded 3.5 μg m -3. The measurements suggest that the environmental conditions in Erfurt and Sokolov produce a low SO 2 oxidation rate and have a high H 2SO 4 neutralization potential. Daily PM 10 concentrations (59.90 μg m -3 in Erfurt and 53.8 μg m -3 in Sokolov) were in the same range for both cities with higher values in winter. Of note was the decrease of all pollutants during the period of observation.

  19. Rhodium-Catalyzed C-S and C-N Functionalization of Arenes: Combination of C-H Activation and Hypervalent Iodine Chemistry.

    PubMed

    Wang, Fen; Yu, Xinzhang; Qi, Zisong; Li, Xingwei

    2016-01-11

    Rhodium-catalyzed sulfonylation, thioetherification, thiocyanation, and other heterofunctionalizations of arenes bearing a heterocyclic directing group have been realized. The reaction proceeds by initial Rh(III) -catalyzed C-H hyperiodination of arene at room temperature followed by uncatalyzed nucleophilic functionalization. A diaryliodonium salt is isolated as an intermediate, which represents umpolung of the arene substrate, in contrast to previous studies that suggested umpolung of the coupling partner. PMID:26538162

  20. Rhodium(III)-Catalyzed Directed ortho-C-H Bond Functionalization of Aromatic Ketazines via C-S and C-C Coupling.

    PubMed

    Wen, Jing; Wu, An; Wang, Mingyang; Zhu, Jin

    2015-11-01

    Described herein is a convenient and efficient method for sulfuration and olefination of aromatic ketazines via rhodium-catalyzed oxidative C-H bond activation. A range of substituted substrates are supported, and a possible mechanism is proposed according to experimental results of kinetic isotopic effect, reversibility studies, and catalysis of rhodacycle intermediate c1. PMID:26417874

  1. Will the S.C.C.'s Decision on Physician-Assisted Death Apply to Persons Suffering from Severe Mental Illness?

    PubMed

    Walker-Renshaw, Barbara; Finley, Margot

    2016-02-01

    In this article, the authors address the question of whether the Supreme Court of Canada's decision in Carter v. Canada leaves open the possibility that persons with severe, treatment-refractory mental illness may lawfully seek a physician-assisted death. If so, how will health care providers distinguish between suicidal ideation and intent that is a symptom of the pathology of a treatable mental illness, on the one hand; and suicidal ideation and intent that is, perhaps, a capable and thoughtful response to a "grievous and irremediable" condition, on the other hand? Mental illness is the most common risk factor for suicide. If physician-assisted death becomes an accepted practice in mental health care, how will that be reconciled with the well-established impetus in mental health care to prevent suicide? The authors consider the competing ethical values of beneficence and promoting patient autonomy, in the context of the recovery movement in mental health care. PMID:27169201

  2. G.I. Joe Meets Barbie, Software Engineer Meets Caregiver: Males and Females in B.C.'s Public Schools and Beyond. BCTF Research Report.

    ERIC Educational Resources Information Center

    Schaefer, Anne C.

    Following a referral from the March 2000 Annual General Meeting of the British Columbia (B.C.) Teachers' Federation, the Spring 2000 Representative Assembly passed a motion that recommended research be collected, conducted, and disseminated on the current status of students in the province. This research report identifies current information on…

  3. Charlotte, N.C.'s Project L.I.F.T.: One Teacher's View of Becoming a Paid Teacher-Leader. An Opportunity Culture Case Study

    ERIC Educational Resources Information Center

    Han, Jiye Grace; Barrett, Sharon Kebschull

    2013-01-01

    Romain Bertrand is a middle school math teacher and Opportunity Culture enthusiast. As the 2012-13 school year wound down, he was already thoroughly looking forward to the next--when he will become a multi-classroom leader at Ranson IB Middle School, taking accountability for the learning results of 700 students. At Ranson, a Project L.I.F.T.…

  4. Prevalence of mandibular fractures reported at C.S.M.S.S Dental College, aurangabad from february 2008 to september 2009

    PubMed Central

    Ghodke, Monali H.; Bhoyar, Subhash C.; Shah, Seemit V.

    2013-01-01

    Aim: The aim of this study is to determine the etiology, frequency of mandibular fractures among different age and sex, to determine the frequency of anatomic distribution, and to report the different modalities of treatment provided to the patients reported at our institution from February 2008 to September 2009. Materials and Methods: All patients fulfilling the selection criteria and having mandible fracture were selected for the study. Patient information was collected by means of a medical data form specifically designed for the present study. The values were subjected to Z and Chi-square tests. Results: Out of 35 patients, thirty one were males (88.57%) and four were females (11.43%) with a male:female ratio of 8:1. We found a peak occurrence in young adults, aged 21-30 years (n = 15, 42.86%). In case of etiology of fracture, road traffic accidents (RTAs) was the most common (n = 25, 71.43%) and condyle was most frequently involved site (n = 19, 38.78%). In most (n = 16, 45.71%) of the patients, an open reduction and rigid internal fixation using bone plate and screws was done. Conclusion: In the present study, the prevalence of mandible fractures was more prevalent in male patients, especially during the 3rd decade of life. The most common cause was road traffic accident and the more frequently affected region was condyle of the mandible. Open reduction and rigid internal fixation using miniplates and screws was the most commonly used treatment. PMID:24778980

  5. Comparison of the kinetics and thermodynamics for methyl radical addition to C=C, C=O, and C=S double bonds.

    PubMed

    Henry, David J; Coote, Michelle L; Gómez-Balderas, Rodolfo; Radom, Leo

    2004-02-18

    The barriers, enthalpies, and rate constants for the addition of methyl radical to the double bonds of a selection of alkene, carbonyl, and thiocarbonyl species (CH(2)=Z, CH(3)CH=Z, and (CH(3))(2)C=Z, where Z = CH(2), O, or S) and for the reverse beta-scission reactions have been investigated using high-level ab inito calculations. The results are rationalized with the aid of the curve-crossing model. The addition reactions proceed via early transition structures in all cases. The barriers for addition of methyl radical to C=C bonds are largely determined by the reaction exothermicities. Addition to the unsubstituted carbon center of C=C double bonds is favored over addition to the substituted carbon center, both kinetically (lower barriers) and thermodynamically (greater exothermicities). The barriers for addition to C=O bonds are influenced by both the reaction exothermicity and the singlet-triplet gap of the substrate. Addition to the carbon center is favored over addition to the oxygen, also both thermodynamically and kinetically. For the thiocarbonyl systems, addition to the carbon center is thermodynamically favored over addition to sulfur. However, in this case, the reaction is contrathermodynamic, addition to the sulfur center having a lower barrier due to spin density considerations. Entropic differences among corresponding addition and beta-scission reactions are relatively minor, and the differences in reaction rates are thus dominated by differences in the respective reaction barriers. PMID:14871104

  6. An Investigation of Two Formal Operational Schemata in Adolescents Enrolled in the I.S.C.S. Classrooms of Three Selected Teachers.

    ERIC Educational Resources Information Center

    Hale, James Patrick

    Reported is an investigation of formal operational thinking, measured by using four Piaget-related tasks, in adolescents. One hundred eight randomly selected eighth-grade students, enrolled in three Intermediate Science Curriculum Study (ISCS) test center classrooms, participated. The students were interviewed using the tasks. A description of the…

  7. Geochemical and isotopic (Sr, O, C, S) evidence for multiple fluid sources for the Muþ barite deposits, SE Anatolia, Turkey

    NASA Astrophysics Data System (ADS)

    Kumral, M.; Baran, A.; Budakoglu, M.

    2009-05-01

    Barite mineralizations are observed in recrystalized and dolomitic limestones relating to Devonian aged Ground Formation, and in forms of veins, clearance filling ; and they are mostly hydrothermal characterized. It was defined by the results of field observations and analysis that barite mineralization is accompanied by the elements like copper, lead and zinc. That 18O and 87Sr/86Sr isotope values of limestones and barites which are wall rocks are very close reminds same origin formation. According to the relations of ore and wall rock, the most natural source that may cause mineralization is Devonian sea water, but mineralization has higher trace element and rare earth element concentrations. That Eu characterizing continental climate from rare earth elements was found high and Ce, characteristic of sea water, was negative preoccupy that mineralization in the area did not create any formation. In addition, considering that high 34S (‰ 17-44) and 18O values (‰ 12-20) and 87Sr/86Sr isotopes characterize the continental crust, a complicate formation mechanism is seen. It is thought that the solution causing mineralization is the Devonian sea water affected from continental crust. 34S ve 18O are enriched when Devonian sea water, in continental crust, enters a hydrothermal cycle which is permanently heatened by granitic intrusion and in consequence of bacterial activities occured during this process. It dissolves and incorporates Ba, Sr, Pb, Cu and Zn during this cycle. Eventually, mineralization occured through impregnation of these elements into piling in parts sedimentation continued.

  8. A mixture of mantle and crustal derived He-Ar-C-S ore-forming fluids at the Baogutu reduced porphyry Cu deposit, western Junggar

    NASA Astrophysics Data System (ADS)

    Cao, MingJian; Qin, KeZhang; Li, GuangMing; Evans, Noreen J.; He, HuaiYu; Jin, LuYing

    2015-02-01

    Most large to huge porphyry Cu deposits (PCDs) are oxidized, making the Baogutu reduced porphyry Cu deposit (RPCD) a relative rarity. CH4-bearing ore-forming fluids formed at several hydrothermal stages, however, their source is still unclear. To address this issue, isotopic investigations of sulfide He-Ar-S and calcite C were conducted. Fluid inclusions hosted in sulfides (arsenopyrite, chalcopyrite and pyrite) showed 3He/4He ratios of 0.06-0.30 Ra (Ra is the 3He/4He ratio of air = 1.39 × 10-6), 40Ar/36Ar of 311-405, 40Ar∗/4He of 0.06-1.01, and F4He ratios of 902-11,074 (sample BGT-Py 2 yielded a ratio of 100), indicating a predominantly crustal source for the fluids with minor mantle input (less than 5%). The δ13C values of carbonate yielded a value of -7.8‰ (n = 3), implying that CO2 was probably sourced from mantle or juvenile lower crust. According to the restricted sulfide δ34S values, the total S isotopic composition of the hydrothermal system was estimated to be 0.0-0.5‰, suggesting that the sulfur was derived from mantle or lower crust magmatic source. According to the published granitoids Nd isotopic compositions at the Baogutu RPCD, fairly young TDM model ages (450-650 Ma) suggest that the granitoids were derived from partial melting of a juvenile basaltic lower crust. Thus, we propose that small proportion of mantle-derived fluids (less than 5%), probably rise up and then mix with the fluids of juvenile lower crust under an extensional tectonic setting, forming the mantle-derived Sr-Nd-Pb-S-C but crustal He-Ar isotopic compositions.

  9. Biological activity at the limits of life: Microbial cycling of C, S and N in cold, permanently stratified, hypersaline Lake Vanda, Antarctica.

    NASA Astrophysics Data System (ADS)

    Joye, S. B.; Schutte, C.; Samarkin, V.; Casciotti, K. L.; Madigan, M.; Saxton, M.

    2014-12-01

    The lakes of the McMurdo Dry Valleys (MCM) are the only perennially ice covered lakes on Earth and are the primary refuge for life in this hyper-arid polar desert. As a result of the ice cover and an uncoupled day/night cycle, the physical and biogeochemical processes in the lakes are highly unusual, with biogeochemical gradients and concentrations of specific compounds often exceeding those found in other aquatic ecosystems on Earth. These lakes are ideal systems for the study of redox-sensitive biogeochemical processes, model systems for understanding the effects of global climate change on polar ecosystems, end-member systems that provide insight into biogeochemical and limnological dynamics in meromictic lakes, analogues for life on other planets, and perfect systems to study microbial life at its thermodynamic limits. Lake Vanda, in the Wright valley, is relatively deep (73 m), hypersaline and has anoxic bottom water. High concentrations of chacotrophic salts results in low water activities that exert further challenges on microbial life. We collected details geochemical profiles of nutrients, major ions, dissolved gases, and redox metabolites and measured rates of microbially-mediated processes that cycle carbon, nitrogen and sulfur in the lakes waters and sediments. Despite the harsh and extreme nature of Lake Vanda and the thermodynamic barriers to microbially-mediated geochemical reactions, microorganisms are not only present in the lake but they mediate a diverse suite of geochemical processes. Statistical correlations between geochemical parameters, microbial activity and microbial community composition shed light on the factors that regulate and limit microbial activity in this unique extreme environment.

  10. Charlotte, N.C.'s Project L.I.F.T.: New Teaching Roles Create Culture of Excellence in High-Need Schools. An Opportunity Culture Case Study

    ERIC Educational Resources Information Center

    Han, Jiye Grace; Barrett, Sharon Kebschull

    2013-01-01

    This case study reports on the work of Denise Watts, who in 2011 was the newly named Project L.I.F.T. executive director and a Charlotte-Mecklenburg Schools zone superintendent. She approached Public Impact for help in meeting the new Project L.I.F.T. (Leadership and Investment for Transformation) goals. Facing urgent needs for real change, Watts…

  11. Prato and Bingel-Hirsch cycloaddition to heptagon-containing LaSc2N@C(s)(hept)-C80: importance of pentalene units.

    PubMed

    Deng, Qingming; Popov, Alexey A

    2015-04-01

    Possible cycloaddition sites in the heptagon-containing fullerene LaSc2N@Cs(hept)-C80 are studied computationally. Thermodynamically controlled Prato addition is predicted to proceed regioselectively across the pentagon/pentagon (p/p) edges, whereas in the kinetically-controlled Bingel-Hirsch reaction the most reactive are carbons next to the p/p edge. PMID:25704065

  12. Charlotte, N.C.'s Project L.I.F.T.: Ranson IB Middle School Launches an Opportunty Culture. An Opportunity Culture Case Study

    ERIC Educational Resources Information Center

    Barrett, Sharon Kebschull; Han, Jiye Grace

    2015-01-01

    Principal Alison Harris is blunt in describing what she confronted on her arrival to Ranson IB Middle School in 2011. "I was placed in what many people would call an impossible situation," she says. During her initial visit to the school in 2009-10, she watched as students changed classes--while teachers pressed against the lockers to…

  13. An Investigation on the Relationship between the School Level of Funding and Performance at K.C.S.E. in Mumias District, Western Province, Kenya

    ERIC Educational Resources Information Center

    Sisungo, Z.; Kaberia, L.; Buhere, P.

    2014-01-01

    The Kenyan government has been spending between 20% to 40% of its revenue on education with the aim to improving access and quality. Much of these resources have been devoted towards establishment and procurement of school inputs such as classrooms, teachers and textbooks. This study investigated the effects of funding on performance in Mumias…

  14. Dicarbonyl­chlorido(phen­oxy­thio­carbonyl-κ2 C,S)bis­(triphenyl­phosphane-κP)molybdenum(II)

    PubMed Central

    Lee, Gene-Hsiang; Wang, Hsiao-Fen; Yih, Kuang-Hway; Huang, Shou-Ling

    2011-01-01

    In the title complex, [Mo(C7H5OS)Cl(C18H15P)2(CO)2], the geometry around the metal atom is a capped octa­hedron. The phen­oxy­thio­carbonyl ligand coordinates the MoII atom through the C and S atoms. A one-dimensional structure is formed by π–π inter­molecular inter­actions and a supra­molecular aggregation is determined by inter­molecular C—H⋯O, C—H⋯Cl, C—H⋯π(arene) hydrogen bonds and CO⋯π(arene) inter­actions [O⋯centroid distances = 3.485 (4) and 3.722 (3) Å]. PMID:21522529

  15. A facile method for the synthesis of copper modified amine-functionalized mesoporous zirconia and its catalytic evaluation in C-S coupling reaction.

    PubMed

    Mallick, Sujata; Rana, Surjyakanta; Parida, Kulamani

    2011-09-28

    A new copper modified amine functionalized zirconia has been synthesized by a co-condensation method using zirconium butoxide and aminopropyltriethoxy-silane (APTES) in the presence of a cationic surfactant CTAB followed by impregnation of copper. Nitrogen adsorption-desorption, X-ray powder diffraction, Fourier-transform infrared spectroscopy (FT-IR), (13)C nuclear magnetic resonance (NMR), scanning electron micrography (SEM), transmittance electron micrography (TEM), thermo gravimetric analysis-differential thermal analysis (TGA-DTA), X-ray photoelectron spectroscopy (XPS) and UV-vis DRS spectroscopic tools are used to characterize the materials. FT-IR and DRS results indicated the incorporation of Cu and amino groups on the surface of zirconia. This Cu-anchored mesoporous material acts as an efficient, reusable catalyst in the aryl-sulfur coupling reaction between aryl iodide and thiophenol for the synthesis of value added diarylsulfides. PMID:21826356

  16. Eye-Tracking Investigations Exploring How Students Learn Geology from Photographs and The Structural Setting of Hydrothermal Gold Deposits in the San Antonio Area, B.C.S., MX

    NASA Astrophysics Data System (ADS)

    Coyan, Joshua

    Geoscience educators commonly teach geology by projecting a photograph in front of the class. Geologic photographs often contain animals, people, and inanimate objects that help convey the scale of features in the photograph. Although scale items seem innocuous to instructors and other experts, the presence of such items is distracting and has a profound effect on student learning behavior. To evaluate how students visually interact with distracting scale items in photographs and to determine if cueing or signaling is an effective means to direct students to pertinent information, students were eye tracked while looking at geologically-rich photographs. Eye-tracking data revealed that learners primarily looked at the center of an image, focused on faces of both humans and animals if they were present, and repeatedly returned to looking at the scale item (distractor) for the duration an image was displayed. The presence of a distractor caused learners to look at less of an image than when a distractor was not present. Learners who received signaling tended to look at the distractor less, look at the geology more, and surveyed more of the photograph than learners who did not receive signaling. The San Antonio area in the southern part of the Baja California Peninsula is host to hydrothermal gold deposits. A field study, including drill-core analysis and detailed geologic mapping, was conducted to determine the types of mineralization present, the types of structures present, and the relationship between the two. This investigation revealed that two phases of mineralization have occurred in the area; the first is hydrothermal deposition of gold associated with sulfide deposits and the second is oxidation of sulfides to hematite, goethite, and jarosite. Mineralization varies as a function of depth, whereas sulfides occurring at depth, while minerals indicative of oxidation are limited to shallow depths. A structural analysis revealed that the oldest structures in the study area include low-grade to medium-grade metamorphic foliation and ductile mylonitic shear zones overprinted by brittle-ductile mylonitic fabrics, which were later overprinted by brittle deformation. Both primary and secondary mineralization in the area is restricted to the later brittle features. Alteration-bearing structures have an average NNW strike consistent with northeast-southwest-directed extension, whereas unaltered structures have an average NNE strike consistent with more recent northwest-southeast-directed extension.

  17. Charlotte, N.C.'s Project L.I.F.T.: Ashley Park PreK-8 Launches Multi-Classroom Leadership and Blended Learning. An Opportunity Culture Case Study

    ERIC Educational Resources Information Center

    Barrett, Sharon Kebschull; Han, Jiye Grace

    2015-01-01

    Tonya Kales came to Ashley Park PreK-8 as its principal (2009-2013), and confronted a school at the end of its rope. Ashley Park was a beautiful facility, but there was no learning going on in the building, it was a chaotic environment for both kids and adults. It was a hostile environment--had adults that were totally incompetent in their…

  18. Sulfur in coal: Model studies of the role of ArS radicals in C-C and C-S bond formation and structural evolution in coal liquefaction

    SciTech Connect

    Alnajjar, M.S.; Franz, J.A.

    1987-06-01

    Experiments in this paper show the importance of thiyl radicals in sulfur containing coals during coal liquefaction processes. The presence of arylthiyl radicals enhances the cleavage of C-C, C=C, and C=C bonds in these otherwise refactory systems. Abstraction reactions, 1,2-phenyl migration from sulfur to carbon and displacement reactions at sulfur may be important mechanisms of structural evolution during liquefaction. In addition to cleavage of arylalkyl structures, the results also show that undesirable retrograde formation of inert diaryl- and triarylmethanes may be a consequence of the presence of sulfur and the attending aryl thiol structures. Thus, while a reaction medium including sulfur and hydrogen has been demonstrated to lead to the enhance cleavage of the bibenzyl model structure the present results suggest that retrograde reactions may be significant undesired pathways in coal liquefaction in the presence of sulfur. 17 refs.

  19. Late Quaternary Normal Faulting and Hanging Wall Basin Evolution of the Southwestern Rift Margin from Gravity and Geology, B.C.S., MX and Exploring the Influence of Text-Figure Format on Introductory Geology Learning

    ERIC Educational Resources Information Center

    Busch, Melanie M. D.

    2011-01-01

    An array of north-striking, left-stepping, active normal faults is situated along the southwestern margin of the Gulf of California. This normal fault system is the marginal fault system of the oblique-divergent plate boundary within the Gulf of California. To better understand the role of upper-crustal processes during development of an obliquely…

  20. Gold deposition by sulfidation of ferrous Fe in the lacustrine sediments of the Pueblo Viejo district (Dominican Republic): The effect of Fe-C-S diagenesis on later hydrothermal mineralization in a Maar-Diatreme complex

    USGS Publications Warehouse

    Kettler, R.M.; Rye, R.O.; Kesler, S.E.; Meyers, P.A.; Polanco, J.; Russell, N.

    1992-01-01

    The Pueblo Viejo district, located in the Cordillera Central of the Dominican Republic, contains large Au-Ag deposits associated with acid-sulfate alteration within spilites, conglomerates and carbonaceous sedimentary rocks that were deposited in a maar-diatreme complex. Much of the Au mineralization occurs in pyritic, carbonaceous siltstones of the Pueblo Viejo Maar-Diatreme Member of the Cretaceous Los Ranchos Formation. Pyrite is the only Fe-bearing phase in mineralized rock, whereas siderite is the dominant Fe-bearing phase in siltstones distal to mineralization. Disseminated pyrite occurs as framboids, cubes, pyritohedra, concretions and cement. Early framboids occur throughout the district. Au occurs as inclusions in later non-framboid disseminated pyrite (NFDP); an occurrence that is interpreted to be indicative of contemporaneous deposition. Pyrite framboids exhibit a wide range of ??34Scdt-values (-17.5 to +4.8???) and are interpreted to have formed during biogenic reduction of pore-water sulfate. The NFDP yield restricted ??34Scdt-values ( x ?? = -5.2???, s = ??2.4???, n = 43) similar to those obtained from later vein pyrite ( x ?? = -6.4???, s = ??1.5???, n = 12). Alunite and barite have ??34S-values ranging from +18.8 to +21.6???. The interpretation that the NFDP, vein pyrite, alunite and barite, and possibly even the framboidal pyrite share a common source of igneous sulfur is supported by the ??34S data. Siderite occurs as concretions and cement, contains abundant Mg (Fe0.75Mg0.19Mn0.03Ca0.02CO3) and has ??13Cpdb- and ??18Osmow-values ranging from -2.5 to +1.1%. and +14.6 to +19.5???, respectively. These data are consistent with the interpretation that the siderite formed in lacustrine sediments and that the carbonate in the siderite is probably methanogenic, although contributions from oxidation of organic matter during biogenic sulfate reduction, thermal decarboxylation of organic matter, or magmatic vapor cannot be ruled out. Disseminated Au mineralization in the sedimentary rocks formed when a hydrothermal fluid encountered reactive Fe2+ in diagenetic siderite. The ensuing pyrite deposition consumed H2S and destabilized the Au (HS)-2 complex, leading to precipitation of Au. The capacity of the sedimentary rocks to consume H2S and precipitate Au was controlled by the amount of non-pyrite Fe present as siderite. The abundance of siderite was controlled by the extent of pyrite formation during diagenesis. ?? 1992.

  1. Riemann-Hypothesis Millennium-Problem(MP) Physics Proof via CATEGORY-SEMANTICS(C-S)/F=C Aristotle SQUARE-of-OPPOSITION(SoO) DEduction-LOGIC DichotomY

    NASA Astrophysics Data System (ADS)

    Baez, J.; Lapidaryus, M.; Siegel, Edward Carl-Ludwig

    2011-03-01

    Riemann-hypothesis physics-proof combines: Siegel-Antonoff-Smith[AMS Joint Mtg.(2002)-Abs.973-03-126] digits on-average statistics HIll[Am. J. Math 123, 3, 887(1996)] logarithm-function's (1,0)-fixed-point base=units=scale-invariance proven Newcomb[Am. J. Math. 4, 39(1881)]-Weyl[Goett. Nachr.(1914); Math. Ann. 7, 313(1916)]-Benford[Proc. Am. Phil. Soc. 78, 4, 51(1938)]-law [Kac, Math. of Stat.-Reasoning(1955); Raimi, Sci. Am. 221, 109(1969)] algebraic-inversion to ONLY Bose-Einstein quantum-statistics(BEQS) with digit d = 0 gapFUL Bose-Einstein Condensation(BEC) insight that digits are quanta are bosons were always digits, via Siegel-Baez category-semantics tabular list-format matrix truth-table analytics in Plato-Aristotle classic "square-of-opposition" : FUZZYICS=CATEGORYICS/Category-Semantics, with Goodkind Bose-Einstein condensation(BEC) ABOVE ground-state with/and Rayleigh(cut-limit of "short-cut method";1870)-Polya(1922)-"Anderson"(1958) localization [Doyle and Snell, Random-Walks and Electrical-Networks, MAA(1981)-p.99-100!!!].

  2. Riemann-Hypothesis Millennium-Problem(MP) Physics Proof via CATEGORY-SEMANTICS(C-S)/F =C Aristotle SQUARE-of-OPPOSITION(SoO) DEduction-LOGIC DichotomY

    NASA Astrophysics Data System (ADS)

    Baez, Joao-Joan; Lapidaryus, Michelle; Siegel, Edward Carl-Ludwig

    2013-03-01

    Riemann-hypothesis physics-proof combines: Siegel-Antono®-Smith[AMS Joint Mtg.(2002)- Abs.973-03-126] digits on-average statistics HIll[Am. J. Math 123, 3, 887(1996)] logarithm-function's (1,0)- xed-point base =units =scale-invariance proven Newcomb [Am. J. Math. 4, 39(1881)]-Weyl[Goett. Nachr.(1914); Math. Ann.7, 313(1916)]-Benford[Proc. Am. Phil. Soc. 78, 4, 51(1938)]-law [Kac,Math. of Stat.-Reasoning(1955); Raimi, Sci. Am. 221, 109(1969)] algebraic-inversion to ONLY Bose-Einstein quantum-statistics(BEQS) with digit d = 0 gapFUL Bose-Einstein Condensation(BEC) insight that digits are quanta are bosons because bosons are and always were quanta are and always were digits, via Siegel-Baez category-semantics tabular list-format matrix truth-table analytics in Plato-Aristotle classic ''square-of-opposition'' : FUZZYICS =CATEGORYICS/Category-Semantics, with Goodkind Bose-Einstein Condensation (BEC) ABOVE ground-state with/and Rayleigh(cut-limit of ''short-cut method''1870)-Polya(1922)-''Anderson''(1958) localization [Doyle and Snell,Random-Walks and Electrical-Networks, MAA(1981)-p.99-100!!!] in Brillouin[Wave-Propagation in Periodic-Structures(1946) Dover(1922)]-Hubbard-Beeby[J.Phys.C(1967)] Siegel[J.Nonxline-Sol.40,453(1980)] generalized-disorder collective-boson negative-dispersion mode-softening universality-principle(G...P) first use of the ``square-of-opposition'' in physics since Plato and Aristote!!!

  3. Cu-catalyzed Fe-driven C(sp)-C(sp) and C(s)p-C(sp2) cross-coupling: an access to 1,3-diynes and 1,3-enynes.

    PubMed

    Ahammed, Sabir; Kundu, Debasish; Ranu, Brindaban C

    2014-08-15

    An efficient Csp-Csp cross-coupling of alkynyl bromide and pinacol ester of alkynyl boronic acid catalyzed by CuFe2O4 nanoparticles has been accomplished in dimethyl carbonate to produce unsymmetric 1,3-diynes. This protocol is also extended for the Csp-Csp2 coupling of alkynyl bromide and alkenyl boronic acid to provide conjugated 1,3-enynes. The aliphatic, aromatic, and heteroaromatic alkynes couple with various substituted alkynyl/alkenyl boronates/boronic acids by this procedure to furnish a library of 1,3-diynes and enynes in high yields. The catalyst was easily separated by an external magnet and recycled 10 times. PMID:25046329

  4. Late Quaternary Normal Faulting and Hanging Wall Basin Evolution of the Southwestern Rift Margin From Gravity and Geology, B.C.S., MX and Exploring the Influence of Text-Figure Format on Introductory Geology Learning

    NASA Astrophysics Data System (ADS)

    Busch, Melanie M. D.

    2011-12-01

    An array of north-striking, left-stepping, active normal faults is situated along the southwestern margin of the Gulf of California. This normal fault system is the marginal fault system of the oblique-divergent plate boundary within the Gulf of California. To better understand the role of upper-crustal processes during development of an obliquely rifted plate margin, gravity surveys were conducted across the normal-fault-bounded basins within the gulf-margin array and, along with optically stimulated luminescence dating of offset surfaces, fault-slip rates were estimated and fault patterns across basins were assessed, providing insight into sedimentary basin evolution. Additionally, detailed geologic and geomorphic maps were constructed along two faults within the system, leading to a more complete understanding of the role of individual normal faults within a larger array. These faults slip at a low rate (0.1--1 mm/yr) and have relatively shallow hanging wall basins (˜500--3000 m). Overall, the gulf-margin faults accommodate protracted, distributed deformation at a low rate and provide a minor contribution to overall rifting. Integrating figures with text can lead to greater science learning than when either medium is presented alone. Textbooks, composed of text and graphics, are a primary source of content in most geology classes. It is essential to understand how students approach learning from text and figures in textbook-style learning materials and how the arrangement of the text and figures influences their learning approach. Introductory geology students were eye tracked while learning from textbook-style materials composed of text and graphics. Eye fixation data showed that students spent less time examining the figure than the text, but the students who more frequently examined the figure tended to improve more from the pretest to the posttest. In general, students tended to examine the figure at natural breaks in the reading. Textbook-style materials should, therefore, be formatted to include a number of natural breaks so that learners can pause to inspect the figure without the risk of losing their place in the reading and to provide a chance to process the material in small chunks. Multimedia instructional materials should be designed to support the cognitive processes of the learner.

  5. The Dramatic Effects of C-S-O-H-Cl on the Melt-Fluid Partitioning of Cl and the Challenge of Accurately Modeling Cl Concentrations of Evolving Magmatic Fluids

    NASA Astrophysics Data System (ADS)

    Webster, J. D.; Sintoni, M. F.; de Vivo, B.

    2007-12-01

    New experimental constraints on the distribution of Cl between Vesuvius phonolite melt and H2O-, CO2-, SO2-, and Cl-bearing vapor, vapor plus saline liquid, or saline liquid have been determined at 200 MPa and 900°C. Some experiments involve melts saturated in all four volatile components. The addition of small quantities of SO2, CO2, and SO2 plus CO2 to fluids dominated by water and alkali chlorides causes dramatic reductions in DXCl (mole fraction Cl in fluid(s)/mole fraction Cl in silicate melt). Experiments with XCO2fluid of 0.15 or XSO2fluid of 0.15 are characterized by values of DXCl that are an order of magnitude lower than those of S- and C-free runs. This observation has important consequences for open systems that exsolve CO2- and/or SO2-enriched fluids "early" in the chemical differentiation of magma. Extrapolation of our experimental results to other pressures and for other melt compositions indicates that CO2- and/or SO2-bearing fluids will not sequester significant abundances of Cl from magma. Thus, CO2- and/or SO2-enriched fluids that exsolve and escape "early" from magma will not dramatically alter the magmatic Cl content. This is consistent with the oft-quoted, general degassing order of: C (first), S, Cl, and H2O (last) associated with decreasing pressure. To apply these new partitioning data to models of the exsolution and chemical evolution of magmatic fluids, they must be integrated with experimental constraints on other parameters that also strongly influence the distribution of Cl between melts and fluids (e.g., pressure, temperature, melt composition, and the Cl content of the bulk system). Expressed as DXCl, published values for Cl partitioning range from 20 (with felsic melts) to ca. 0.4 (with mafic melts), but DXCl is a complex function of these parameters. For example, DXCl increases by an order of magnitude as temperature decreases from 1000° to 800°C with vapor-saturated felsic melts at 200 MPa. Conversely, DXCl decreases by an order of magnitude in experiments involving a pressure reduction of 280 to 80 MPa with phonolite melt saturated in Cl-bearing aqueous fluid(s), but other experiments show that DXCl increases with decreasing pressure. DXCl also varies positively with the Cl concentration of the bulk system. In addition, the chemical evolution of fluid-saturated magma from basaltic to rhyolitic melt compositions also involves an order of magnitude increase in DXCl with all other parameters equal. In summary, as magmas ascend through the crust, cool, and differentiate, values of DXCl (and hence the Cl content of coexisting fluids) tend to increase due to the attendant reduction in temperature, because of the evolution of magma to increasingly felsic compositions, and due to the potential loss of CO2 and/or SO2 from magma to fluids that exsolve and escape "early". Conversely, values of DXCl (and the Cl content of coexisting fluids) may also tend to decrease because of the reduction in pressure during ascent. Moreover, the crystallization of Cl-free and Cl-poor minerals will tend to increase the Cl content of the magma and increase values of DXCl; whereas, the loss of Cl to C- and S-poor aqueous fluid(s) in open magmatic systems will reduce the Cl content of the system and tend to reduce DXCl during late-stage fluid-melt interactions.

  6. Bis(carbonyl-κC)(N,N-dimethyl­thio­carbamoyl-κ2 C,S)(pyridine-2-thiol­ato-κ2 N,S)(triphenyl­phosphine-κP)molybdenum(II)

    PubMed Central

    Yih, Kuang-Hway; Wang, Hsiao-Fen; Lee, Gene-Hsiang

    2010-01-01

    There are two independent mol­ecules with similar configurations in the title complex, [Mo(C3H6NS)(C5H4NS)(C18H15P)(CO)2]. The geometry around the metal atom is that of a capped octa­hedron. The thio­cabamoyl and pyridine-2-thiol­ate ligands coordinate to the molybdenum metal center through the C and S atoms, and N and S atoms, respectively. NMR, IR and MS analyses are in agreement with the structure of the title compound. PMID:21587354

  7. Rapid analysis for metabolites of 11C-labelled drugs: fate of [11C]-S-4-(tert.-butylamino-2-hydroxypropoxy)-benzimidazol-2-one in the dog.

    PubMed

    Jones, H A; Rhodes, C G; Law, M P; Becket, J M; Clark, J C; Boobis, A R; Taylor, G W

    1991-10-01

    Positron emission tomography (PET) requires the use of compounds labelled with short-lived, positron-emitting isotopes (e.g., t1/2 of 11C approximately 120 min). As the concentration of unbound, non-metabolised drug is required as the input function for modeling, this presents particular problems for the study of the kinetics and metabolism of such compounds. We have now developed a rapid extraction procedure, followed by high-performance liquid chromatography using a short analytical column coupled to an on-line gamma-detector to determine the metabolism and kinetics of a non-selective beta-adrenergic antagonist of high affinity, S-4-(tert.-butylamino-2-hydroxypropoxy)benzimidazol-2-one. This antagonist is potentially well suited to the non-invasive localisation of beta-receptors in vivo. The ligand was rapidly taken up into the beta-receptor pool or excreted in urine, with less than 5% of the drug converted to metabolites. Plasma protein binding was only 16%. No significant metabolism of the ligand was observed in the anaesthetised dog, and, therefore, no correction for blood metabolite concentration is required for kinetic analysis of the 11C-labelled ligand during PET studies in this species. The analytical method reported here should be widely applicable: quantification of metabolites enables accurate estimation of the input function and is critical to the interpretation of PET data. PMID:1686775

  8. Lasp1 gene disruption is linked to enhanced cell migration and tumor formation Address for reprint requests and other correspondence: C. S. Chew, Inst. of Molecular Medicine and Genetics, Sanders R&E Bldg., Rm. CB 2803, Medical College of Georgia, Augusta, GA 30912-3175 (e-mail: cchew@mcg.edu).

    PubMed Central

    Zhang, Han; Chen, Xunsheng; Bollag, Wendy B.; Bollag, Roni J.; Sheehan, Daniel J.; Chew, Catherine S.

    2009-01-01

    Lasp1 is an actin-binding, signaling pathway-regulated phosphoprotein that is overexpressed in several cancers. siRNA knockdown in cell lines retards cell migration, suggesting the possibility that Lasp1 upregulation influences cancer metastasis. Herein, we utilized a recently developed gene knockout model to assess the role of Lasp1 in modulating nontransformed cell functions. Wound healing and tumor initiation progressed more rapidly in Lasp1−/− mice compared with Lasp1+/+ controls. Embryonic fibroblasts (MEFs) derived from Lasp1−/− mice also migrated more rapidly in vitro. These MEFs characteristically possessed increased focal adhesion numbers and displayed more rapid attachment compared with wild-type MEFs. Differential microarray analyses revealed alterations in message expression for proteins implicated in cell migration, adhesion, and cytoskeletal organization. Notably, the focal adhesion protein, lipoma preferred partner (LPP), a zyxin family member and putative Lasp1 binding protein, was increased about twofold. Because LPP gene disruption reduces cell migration, we hypothesize that LPP plays a role in enhancing the migratory capacity of Lasp1−/− MEFs, perhaps by modifying the subcellular localization of other motility-associated proteins. The striking contrast in the functional effects of loss of Lasp1 in innate cells compared with cell lines reveals distinct differences in mechanisms of motility and attachment in these models. PMID:19531578

  9. Total Syntheses and Initial Evaluation of [Ψ[C(=S)NH]Tpg4]vancomycin, [Ψ[C(=NH)NH]Tpg4]vancomycin, [Ψ[CH2NH]Tpg4]vancomycin and their (4-Chlorobiphenyl)methyl Derivatives: Synergistic Binding Pocket and Peripheral Modifications for the Glycopeptide Antibiotics

    PubMed Central

    Okano, Akinori; Nakayama, Atsushi; Wu, Kejia; Lindsey, Erick A.; Schammel, Alex W.; Feng, Yiqing; Collins, Karen C.

    2015-01-01

    Full details of studies are disclosed on the total synthesis of binding pocket analogues of vancomycin, bearing the peripheral L-vancosaminyl-1,2-D-glucosyl disaccharide, that contain changes to a key single atom in the residue 4 amide (residue 4 carbonyl O → S, NH, H2) designed to directly address the underlying molecular basis of resistance to vancomycin. Also disclosed are studies piloting the late stage transformations conducted on the synthetically more accessible C-terminus hydroxymethyl aglycon derivatives and full details of the peripheral chlorobiphenyl functionalization of all the binding pocket modified vancomycin analogues designed for dual D-Ala-D-Ala/D-Ala-D-Lac binding are reported. Their collective assessment indicate that combined binding pocket and chlorobiphenyl peripherally modified analogues exhibit a remarkable spectrum of antimicrobial activity (VSSA, MRSA, VanA and VanB VRE) and impressive potencies against both vancomycin-sensitive and vancomycin-resistant bacteria (MICs = 0.06–0.005 μg/mL and 0.5–0.06 μg/mL for the amidine and methylene analogues, respectively) and likely benefit from two independent and synergistic mechanisms of action, only one of which is dependent on D-Ala-D-Ala/D-Ala-D-Lac binding. Such analogues are likely to display especially durable antibiotic activity not prone to rapidly acquired clinical resistance. PMID:25750995

  10. Blending soil conservation with production: Assessment of diverse crop rotations under no-till soil management for agronomic yield and soil C sequestration

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Diversified crop rotations, which reduce risk associated with adoption of no-till soil management, may influence soil C sequestration and soil quality. This study measured effects of corn-soybean (C-S), corn-soybean-oat/pea hay (C-S-H), or corn-soybean-oat/pea hay-alfalfa-alfalfa (C-S-H-A-A) annual...

  11. The effect of chronic osmotic disturbance on the concentrations of cations in cerebrospinal fluid.

    PubMed

    Bradbury, M W; Kleeman, C R

    1969-09-01

    1. Adult cats were rendered hypo- and hypernatraemic by peritoneal dialysis. These states were maintained for periods of 2-5 days.2. The concentrations in cerebrospinal fluid (c.s.f.) of the cations, potassium, calcium and magnesium all decreased in the hyponatraemic animals and increased in the hypernatraemic animals. These shifts in c.s.f. cation concentrations did not relate to plasma changes in the same cations, which were often in the opposite direction.3. The relations of the cation concentrations to c.s.f. sodium were not linear and, in the cases of calcium and magnesium, the relevant cation concentration related better to the square rather than the first power of the c.s.f. sodium concentration.4. Brain water changed much less in the hypo- and hypernatraemic animals than might be anticipated from the shifts in blood osmolarity, plasma sodium concentration and muscle water.5. Isotonicity of the fluids in brain with blood plasma and c.s.f. appeared to be largely maintained by loss or gain of sodium and chloride ions by this tissue.6. The c.s.f. results may be partly due to a constant influx of the cation in question being diluted with more formed c.s.f. in hyponatraemia and less c.s.f. in hypernatraemia, but the deviations from linearity in the plots of c.s.f. cation against c.s.f. sodium suggest the influence of other factors. PMID:5352043

  12. 77 FR 63419 - Unblocking of Specially Designated Nationals and Blocked Persons Pursuant to the Foreign...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-10-16

    ... the Kingpin Act: Individuals 1. ROMERO BARRERA, Benedicto, c/o AGROFUTURO R.H. Y CIA. S.C.S., Medellin...) (individual) . Entities 1. AGROFUTURO R.H. Y CIA. S.C.S., Calle 80 Sur No. 47D-65 Bod. 114, Medellin, Colombia..., Carlos Arturo, c/o AGROFUTURO R.H. Y CIA. S.C.S., Medellin, Colombia; c/o COMERCIALIZADORA...

  13. Susceptibility Testing

    MedlinePlus

    ... page helpful? Also known as: Sensitivity Testing; Drug Resistance Testing; Culture and Sensitivity; C & S; Antimicrobial Susceptibility Formal name: Bacterial and Fungal Susceptibility Testing Related tests: Urine Culture ; ...

  14. X-ray photoelectron spectroscopic investigation of nanocrystalline calcium silicate hydrates synthesised by reactive milling

    SciTech Connect

    Black, Leon . E-mail: l.black@shu.ac.uk; Garbev, Krassimir; Beuchle, Guenter; Stemmermann, Peter; Schild, Dieter

    2006-06-15

    X-ray photoelectron spectroscopy (XPS) has been used to analyse a series of mechanochemically synthesised, nanocrystalline calcium silicate hydrates (C-S-H). The samples, with Ca/Si ratios of 0.2 to 1.5, showed structural features of C-S-H(I). XPS analysis revealed changes in the extent of silicate polymerisation. Si 2p, Ca 2p and O 1s spectra showed that, unlike for the crystalline calcium silicate hydrate phases studied previously, there was no evidence of silicate sheets (Q{sup 3}) at low Ca/Si ratios. Si 2p and O 1s spectra indicated silicate depolymerisation, expressed by decreasing silicate chain length, with increasing C/S. In all spectra, peak narrowing was observed with increasing Ca/Si, indicating increased structural ordering. The rapid changes of the slope of FWHM of Si 2p, {delta} {sub Ca-Si} and {delta} {sub NBO-BO} as function of C/S ratio indicated a possible miscibility gap in the C-S-H-solid solution series between C/S 5/6 and 1. The modified Auger parameter ({alpha}') of nanocrystalline C-S-H decreased with increasing silicate polymerisation, a trend already observed studying crystalline C-S-H. Absolute values of {alpha}' were shifted about - 0.7 eV with respect to crystalline phases of equal C/S ratio, due to reduced crystallinity.

  15. Developing Consumer/Survivor/Recovering Voice and Its Impact on Services and Research: Our Experience with the SAMHSA Women, Co-Occurring Disorders and Violence Study

    ERIC Educational Resources Information Center

    Mockus, Susan; Mars, Laura Cinq; Ovard, Dorothy Guazzo; Mazelis, Ruta; Bjelajac, Paula; Grady, Janice; LaClair, Christine; Livingston, Cardenia; Slavin, Sharon; Williams, Susan; McKinney, Jacki

    2005-01-01

    Integrating consumer/survivor/recovering (C/S/R) women in the Substance Abuse and Mental Health Services Administration's Women, Co-Occurring Disorders and Violence Study involved both struggles and growth. The C/S/R women and all of our professional allies, both individually and collectively, greatly enhanced the study by overcoming what earlier…

  16. Chiari Malformation: Treatment

    MedlinePlus

    ... endorse any doctors, procedures, or products. © 2012 C&S Patient Education Foundation, ® Treatment Options Patients evaluated for Chiari-like ... when there is a significant syrinx © 2012 C&S Patient Education Foundation, ® This presentation is for informational purposes, consult ...

  17. A realistic molecular model of cement hydrates

    PubMed Central

    Pellenq, Roland J.-M.; Kushima, Akihiro; Shahsavari, Rouzbeh; Van Vliet, Krystyn J.; Buehler, Markus J.; Yip, Sidney; Ulm, Franz-Josef

    2009-01-01

    Despite decades of studies of calcium-silicate-hydrate (C-S-H), the structurally complex binder phase of concrete, the interplay between chemical composition and density remains essentially unexplored. Together these characteristics of C-S-H define and modulate the physical and mechanical properties of this “liquid stone” gel phase. With the recent determination of the calcium/silicon (C/S = 1.7) ratio and the density of the C-S-H particle (2.6 g/cm3) by neutron scattering measurements, there is new urgency to the challenge of explaining these essential properties. Here we propose a molecular model of C-S-H based on a bottom-up atomistic simulation approach that considers only the chemical specificity of the system as the overriding constraint. By allowing for short silica chains distributed as monomers, dimers, and pentamers, this C-S-H archetype of a molecular description of interacting CaO, SiO2, and H2O units provides not only realistic values of the C/S ratio and the density computed by grand canonical Monte Carlo simulation of water adsorption at 300 K. The model, with a chemical composition of (CaO)1.65(SiO2)(H2O)1.75, also predicts other essential structural features and fundamental physical properties amenable to experimental validation, which suggest that the C-S-H gel structure includes both glass-like short-range order and crystalline features of the mineral tobermorite. Additionally, we probe the mechanical stiffness, strength, and hydrolytic shear response of our molecular model, as compared to experimentally measured properties of C-S-H. The latter results illustrate the prospect of treating cement on equal footing with metals and ceramics in the current application of mechanism-based models and multiscale simulations to study inelastic deformation and cracking. PMID:19805265

  18. Design and Implementation of Network Management System Based on Mixed-mode

    NASA Astrophysics Data System (ADS)

    Wei, Xianmin

    With the growth of network scale size, structure is getting more and more sophisticated, how to effectively manage the network has been increasingly paid attention to. Development of network management systems, there are mainly two system models, that is, C/S mode and B/S mode. This paper focuses on analysis of advantages and disadvantages in the C/S mode and B/S mode, design and implementation network management system based on the mixed mode with C/S mode and B/S mode.

  19. Mild Cognitive Impairment and Progession to Dementia: New Findings

    MedlinePlus

    ... Karceski, MD Mild cognitive impairment and progression to dementia New findings John C.S. Breitner, MD, MPH WHAT ... many people with MCI go on to develop dementia after a few years. But other people show ...

  20. 77 FR 14593 - Unblocking of Specially Designated Nationals and Blocked Persons Pursuant to Executive Order 12978

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-12

    ...) (``IEEPA''), issued Executive Order 12978 (60 FR 54579, October 24, 1995) (the ``Order''). In the Order...) (individual) ] 2. CARRERO BURBANO, Emma Alexandra, c/o DROMARCA Y CIA. S.C.S., Bogota, Colombia; c/o...

  1. Parents Often Don't Get Rid of Leftover Prescription Opioids

    MedlinePlus

    ... what to do with leftover medication," said Sarah Clark, co-director of the C.S. Mott Children's Hospital ... opportunity to prevent prescription drug misuse among children," Clark added in a statement from the University of ...

  2. 12 CFR 560.31 - Election regarding categorization of loans or investments and related calculations.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ...) If a loan or other investment is authorized under more than one section of the HOLA, as amended, or... with HOLA section 5(c)'s investment limitations only to the extent that funds have been advanced...

  3. Zw 229-15 returning to higher X-ray flux state

    NASA Astrophysics Data System (ADS)

    Edelson, Rick; Mushotzky, Richard

    2011-07-01

    An earlier telegram (ATel #3458) reported that the narrow-line Seyfert 1 galaxy Zw 229-15 (19h05m25.9s +42d27m40s) exhibited a dramatic decrease in X-ray flux during Swift monitoring, with the count rate dropping from a mean of 0.096 c/s during the ~18 days from May 29 through June 17 to a mean of 0.026 c/s during the ~17 days from June 18 through July 5. (All dates/times UT.) The maximum count rate was 0.172 c/s at 2011 June 2 22:35 and the minimum was 0.005 c/s at June 27 00:23.

  4. 77 FR 61581 - Notice of Advisory Committee Closed Meeting; U.S. Strategic Command Strategic Advisory Group

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-10-10

    ..., Command and Control, Science and Technology, Missile Defense. Meeting Accessibility: Pursuant to 5 U.S.C...'s FACA Database-- https://www.fido.gov/facadatabase/public.asp . Written statements that do...

  5. Chiari Malformation: Symptoms

    MedlinePlus

    ... may cause tinnitus (ringing in the ears), depth perception, running into walls and tripping. © 2012 C&S Patient ... Of or pertaining to the mental processes of perception, memory, judgment, and reasoning What We Know: Many ...

  6. The Copper-nicotinamide complex: sustainable applications in coupling and cycloaddition reactions

    EPA Science Inventory

    Crystalline copper (II)-nicotinamide complex, synthesized via simple mixing of copper chloride and nicotinamide solution at room temperature, catalyzes the C-S, C-N bond forming and cycloaddition reactions under a variety of sustainable reaction conditions.

  7. 12 CFR 160.31 - Election regarding categorization of loans or investments and related calculations.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... section of the HOLA, as amended, or this part, a Federal savings association may designate under which... purposes of calculating compliance with HOLA section 5(c)'s investment limitations only to the extent...

  8. 12 CFR 160.31 - Election regarding categorization of loans or investments and related calculations.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... section of the HOLA, as amended, or this part, a Federal savings association may designate under which... purposes of calculating compliance with HOLA section 5(c)'s investment limitations only to the extent...

  9. 12 CFR 560.31 - Election regarding categorization of loans or investments and related calculations.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ...) If a loan or other investment is authorized under more than one section of the HOLA, as amended, or... with HOLA section 5(c)'s investment limitations only to the extent that funds have been advanced...

  10. 12 CFR 560.31 - Election regarding categorization of loans or investments and related calculations.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ...) If a loan or other investment is authorized under more than one section of the HOLA, as amended, or... with HOLA section 5(c)'s investment limitations only to the extent that funds have been advanced...

  11. 12 CFR 160.31 - Election regarding categorization of loans or investments and related calculations.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... section of the HOLA, as amended, or this part, a Federal savings association may designate under which... purposes of calculating compliance with HOLA section 5(c)'s investment limitations only to the extent...

  12. 12 CFR 560.31 - Election regarding categorization of loans or investments and related calculations.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ...) If a loan or other investment is authorized under more than one section of the HOLA, as amended, or... with HOLA section 5(c)'s investment limitations only to the extent that funds have been advanced...

  13. 12 CFR 560.31 - Election regarding categorization of loans or investments and related calculations.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ...) If a loan or other investment is authorized under more than one section of the HOLA, as amended, or... with HOLA section 5(c)'s investment limitations only to the extent that funds have been advanced...

  14. The effects of moisture on the microstructure of cement-based materials. Progress report

    SciTech Connect

    Jennings, H.M.

    1993-07-15

    New information about shrinkage at the microstructural level has been acquired. Experiments and computer analysis serve as a basis for modeling. Some highlights: C-S-H (shrinking phase) shrinks and values for dimensional change are being determined. There may be two types of C-S-H, only one of which shrinks. All other phases serve as restraints to shrinkage. Pores expand on drying and therefore may be a mechanism for the ``size effect``, in addition to microcracks.

  15. Enantioselective autocatalysis. III. Configurational and conformational studies on a 1,4-benzodiazepinooxazole derivative

    NASA Astrophysics Data System (ADS)

    Miller, Benjamin L.; Bonner, William A.

    1995-12-01

    We report here on configurational and conformational studies undertaken on the bromofluoro-1,4-benzodiazepinooxazole derivative I, which has previously been found capable of undergoing total spontaneous resolution under racemizing conditions. Due to its bridgehead N-atom I may exist in any of four diastereomeric forms,C r N r (orC s N s ) andC r N s (orC s N r ). Molecular mechanics calculations revealed that in their lowest energy conformations theC r N r (orC s N s ) diastereomers were favored over theC r N s (orC s N r ) diastereomers by some 3.42 kcal/mol, while semi-empirical quantum mechanical calculations indicated heats of formation also favoring theC r N (orC s N s ) diastereomers by 3.83 kcal/mol. The1H NMR spectra of the three crystalline modifications (α, β andγ) of I were examined in acetone, and found to be identical. These data, combined with the results of the above calculations, suggest that I exists in methanol or methanol-acetone solutions as theC r N (orC s N s ) enantiomer prior to its racemization.

  16. Structures and energies of coadsorbed CO and H2 on Fe5C2(001), Fe5C2(110), and Fe5C2(100).

    PubMed

    Cao, Dong-Bo; Zhang, Fu-Qiang; Li, Yong-Wang; Wang, Jianguo; Jiao, Haijun

    2005-06-01

    Density functional theory calculations have been carried out on the CO/H2 coadsorption on the (001), (110), and (100) surfaces of Fe5C2 for the understanding of the Fischer-Tropsch synthesis (FTS) mechanism. The stable surface species changes with the variation of the H2 and CO coverage. Along with dissociated hydrogen and adsorbed CO in 2-, 3-, and 4-fold configurations, methylidyne (C(s)H) (C(s), surface carbon), ketenylidene (C(s)CO), ketenyl (C(s)HCO), ketene (C(s)H2CO), and carbon suboxide (C(s)C2O2) are computed as thermodynamically stable surface species on Fe5C2(001) and Fe5C2(110) containing both surface iron and carbon atoms. These surface carbon species can be considered as the preliminary stages for FTS. On Fe5C2(100) with only iron atoms on the surface layer, the stable surface species is dissociated hydrogen and CO with top and 2-fold configurations. The bonding nature of these adsorbed carbon species has been analyzed. PMID:16852330

  17. Constitutive activation of Stat5 promotes its cytoplasmic localization and association with PI3-kinase in myeloid leukemias.

    PubMed

    Harir, Noria; Pecquet, Christian; Kerenyi, Marc; Sonneck, Karoline; Kovacic, Boris; Nyga, Remy; Brevet, Marie; Dhennin, Isabelle; Gouilleux-Gruart, Valerie; Beug, Hartmut; Valent, Peter; Lassoued, Kaiss; Moriggl, Richard; Gouilleux, Fabrice

    2007-02-15

    Persistent activation of Stat5 is frequently found in hematologic neoplasms. Studies conducted with constitutively active Stat5 mutants (Stat51*6 and cS5F) have shown that deregulated Stat5 activity promotes leukemogenesis. To investigate the oncogenic properties of these mutants, we used cS5F-expressing bone marrow cells which induce a multilineage leukemia when transplanted into recipient mice. Here, we show by immunocytochemistry that cS5F is localized mainly in the cytoplasmic compartment of leukemic cells, suggesting that the transforming nature of cS5F may be associated with a cytoplasmic function. In support of this hypothesis, we found that cS5F forms a complex with the p85 subunit of the phosphatidylinositol 3-kinase (PI3-K) and the scaffolding adapter Gab2 in leukemic bone marrow cells, resulting in the activation of Akt/PKB, a crucial downstream target of PI3-K. By using transducible TAT-Gab2 or TAT-Akt recombinant proteins, we were able to demonstrate that activation of the PI3-kinase/Akt pathway by cS5F molecules through Gab2 is essential for induction of cell growth. We also found that persistently phosphorylated Stat5 in primary cells from patients with myeloid leukemias has a cytoplasmic localization. These data suggest that oncogenic Stat5 proteins exert dual transforming capabilities not only as transcriptional activators but also as cytoplasmic signaling effectors. PMID:17038539

  18. Tailoring magnetic and photoluminescence properties in ZnS/ZnO core/shell nanostructures through Cr doping

    NASA Astrophysics Data System (ADS)

    Chawla, Santa; Sharma, Simmi; Kotnala, R. K.

    2013-11-01

    Work on doped inverted core/shell semiconductor structure and study of their magnetic and luminescence properties is very rare. We have successfully prepared core/shell (C/S) nanostructure of important semiconductors ZnS core/ZnO shell with doping of chromium in both core and shell regions for tailoring magnetic and luminescence properties. Cooperative exchange of pinned spins at the interface of core and shell magnetic regions lead to ferromagnetism in ZnS:Cr/ZnO:Cr C/S nanoparticles (NP) at room temperature. Ferromagnetic interaction enhances at low temperature. Growth of hexagonal ZnO shell on cubic ZnS NPs in coprepitous aqueous solution has been confirmed by XRD and HRTEM analysis. Substitutional transition metal Cr in ZnS core and/or ZnO shell region could induce magnetic moments, create spin ordering and pinning while on C/S interface and also domain alignment leading to different magnetic states in varied C/S architecture. Cr also induces blue photoluminescence in doped ZnS/ZnO C/S NPs thus paving a possibility of tailoring multifunctional properties in C/S semiconductors architecture.

  19. Interaction grand potential between calcium-silicate-hydrate nanoparticles at the molecular level.

    PubMed

    Bonnaud, Patrick A; Labbez, Christophe; Miura, Ryuji; Suzuki, Ai; Miyamoto, Naoto; Hatakeyama, Nozomu; Miyamoto, Akira; Van Vliet, Krystyn J

    2016-02-21

    Calcium-silicate-hydrate (or C-S-H), an inosilicate, is the major binding phase in cement pastes and concretes and a porous hydrated material made up of a percolated and dense network of crystalline nanoparticles of a mean apparent spherical diameter of ∼5 nm that are each stacks of multiple C-S-H layers. Interaction forces between these nanoparticles are at the origin of C-S-H chemical, physical, and mechanical properties at the meso- and macroscales. These particle interactions and the resulting properties may be affected significantly by nanoparticle density and environmental conditions such as the temperature, relative humidity, or concentration of chemical species in the bulk solution. In this study, we combined grand canonical Monte Carlo simulations and an extension of the mean force integration method to derive the pair potentials. This approach enables realistic simulation of the physical environment surrounding the C-S-H particles. We thus constructed the pair potentials for C-S-H nanoparticles of defined chemical stoichiometry at 10% relative humidity (RH), varying the relative crystallographic orientations at a constant particle density of ρpart ∼ 2.21 mmol L(-1). We found that cohesion between nanoparticles is affected strongly by both the aspect ratio and the crystallographic misorientation of interacting particles. This method and the findings underscore the importance of accounting for relative dimensions and orientation among C-S-H nanoparticles in descriptions of physical and simulated multiparticle aggregates or mesoscale systems. PMID:26866999

  20. Cyclic adenosine 3', 5'-monophosphate in cerebrospinal fluid during thermoregulation and fever.

    PubMed Central

    Dascombe, M J; Milton, A S

    1976-01-01

    1. Samples of cerebrospinal fluid (c.s.f.) have been taken from the cisterna magna of unanaesthetized cats, whilst rectal temperature was recorded, during exposure of the animals to various ambient temperatures and during fever induced by pyrogen. The concentration of adenosine 3', 5'-monophosphate (cyclic AMP) in samples of c.s.f. has been assayed. 2. Cats exposed to low ambient temperatures (-2 to +2 degrees C) for 3 h maintained body temperature by both behavioural and autonomic heat gain activity. Exposure of cats to high ambient temperatures (44 - 45 degrees C) for 3.5 h caused a rise in body temperatures of about 2.5 degrees C, despite behavioural and autonomic heat loss activity. Neither cold nor heat stress had a significant effect on c.s.f. cyclic AMP. 3. Fever induced by intravenous Shigella dysenteriae (2 and 20 mug/kg) was associated with a dose-related increase in the concentration of cyclic AMP in c.s.f. Paracetamol (75 mg/kg) injected I.P. before the onset of fever, suppressed the increase in both temperature and c.s.f. cyclic AMP in response to pyrogen. Paracetamol (50 and 100 mg/kg), injected after the onset of fever, caused a fall in temperature, which was not associated with a decrease in the concentration of cyclic AMP in c.s.f. 4. Fever induced in cats by intravenous Shigella dysenteriae (20 mug/kg) was associated with an increase in the concentration of cyclic AMP in plasma as well as in c.s.f. 5. The sodium salt of cyclic AMP (0.1-10 mg/kg) injected I.V. into unanaesthetized cats caused a dose-related hypothermia, which was associated with autonomic heat loss activity and a dose-related increase in the concentration of cyclic AMP in cisternal c.s.f., which was not mimicked by adenosine. 6. It is concluded that the raised concentrations of cyclic AMP in c.s.f., in response to pyrogen I.V., do not mediate fever in the cat and that the concentration of cyclic AMP in cisternal c.s.f. may be affected by changes in the plasma concentration of the

  1. Studies of the development of brain barrier systems to lipid insoluble molecules in fetal sheep.

    PubMed Central

    Dziegielewska, K M; Evans, C A; Malinowska, D H; Møllgård, K; Reynolds, J M; Reynolds, M L; Saunders, N R

    1979-01-01

    1. The development of the blood-brain and blood-c.s.f barriers to lipid insoluble substances of different molecular radii has been studied in fetal sheep, early (60 days) and late (125 days) in gestation, using labelled erythritol (C14), sucrose (3H or 14C), inulin (3H or 14C) and albumin (125I), or albumin and IgG detected by immunoassay. 2. Morphological studies of fetal brain and choroid plexus at the same gestational stages were carried out using thin section electron microscopy and the freeze fracture techniques. 3. Penetration of markers into c.s.f. was substantially greater at 60 days than at 125 days, but at both ages the steady-state level achieved appeared to be related to molecular size. 4. A simple model describing penetration from blood into c.s.f. at 60 days is proposed. It involves the assumption that c.s.f. and brain extracellular fluid are effectively separate compartments; morphological and permeability data which supports this assumption is presented. The data for c.s.f. at 60 days are consistent with the suggestion that the markers penetrate into c.s.f. by diffusion and are not restricted by small pores in the interface between blood and c.s.f. 5. The reduction in penetration which occurred by 125 days for all markers except erythritol appears to be accounted for by an increase in the sink effect and a decrease in the effective surface area for exchange between blood and c.s.f. 6. Intercellular tight junctions of both cerebral endothelial cells and choroid plexus epithelial cells were well formed at 60 days gestation. There was no change in junctional characteristics previously thought to correlate with transepithelial permeability (tight junction depth and strand number) between the two ages studied, although there were marked changes in permeability. 7. Evidence is advanced in support of the hypothesis that in the fetus much of the penetration of lipid insoluble non-polar substances across the blood-c.s.f. barrier and perhaps across the blood

  2. Differences in airway reactivity in normal and allergic sheep after exposure to sulfur dioxide

    SciTech Connect

    Abraham, W.M.; Oliver, W. Jr.; Welker, M.J.; King, M.M.; Wanner, A.; Sackner, M.A.

    1981-12-01

    The effect of breathing 5 ppm sulfur dioxide (SO/sub 2/) on airway reactivity was studied in both normal and allergic conscious sheep. Allergic sheep were defined as animals in which inhalation of Axcaris suum extract resulted in bronchospasm as evidenced by an increase in mean pulmonary flow resistance (RL), hyperinflation, and a fall in dynamic compliance. Airway reactivity was assessed by measuring the increase of RL after 18 breaths of 0.25% carbachol (c), from an initial RL value obtained after 18 breaths of buffered saline (s) (RL(c-s)). RL and RL(c-s) were determined prior to, immediately after, and 24 h after exposure to 5 ppm SO/sub 2/ for 4 h. In both groups RL remained unchanged after SO/sub 2/ exposure. Prior to exposure, RL(c-s) was not significantly different in seven normal (0.3 +/- 0.1) and seven allergic sheep (0.4 +/- 0.2 (SD) cmH/sub 2/O.l/sup -1/.s), and there was no significant change in RL (c-s) immediately after SO/sub 2/ exposure in either group. Twenty-four h later, RL(c-s) RL(c-s) increased to 0.7 +/- 0.8 (P < 0.2) in normal and to 1.8 +/- 0.9 cmH/sub 2/O.l/sup -1/.s (P < 0.01) in allergic sheep. Because the increase in RL(c-s) after 24 h was greater (P < 0.01) in allergic than in normal sheep, we conclude that SO/sub 2/ exposure increased airway reactivity more in the former than in the latter.

  3. Monte Carlo evaluation of the convolution/superposition algorithm of Hi-Art tomotherapy in heterogeneous phantoms and clinical cases

    SciTech Connect

    Sterpin, E.; Salvat, F.; Olivera, G.; Vynckier, S.

    2009-05-15

    The reliability of the convolution/superposition (C/S) algorithm of the Hi-Art tomotherapy system is evaluated by using the Monte Carlo model TomoPen, which has been already validated for homogeneous phantoms. The study was performed in three stages. First, measurements with EBT Gafchromic film for a 1.25x2.5 cm{sup 2} field in a heterogeneous phantom consisting of two slabs of polystyrene separated with Styrofoam were compared to simulation results from TomoPen. The excellent agreement found in this comparison justifies the use of TomoPen as the reference for the remaining parts of this work. Second, to allow analysis and interpretation of the results in clinical cases, dose distributions calculated with TomoPen and C/S were compared for a similar phantom geometry, with multiple slabs of various densities. Even in conditions of lack of lateral electronic equilibrium, overall good agreement was obtained between C/S and TomoPen results, with deviations within 3%/2 mm, showing that the C/S algorithm accounts for modifications in secondary electron transport due to the presence of a low density medium. Finally, calculations were performed with TomoPen and C/S of dose distributions in various clinical cases, from large bilateral head and neck tumors to small lung tumors with diameter of <3 cm. To ensure a ''fair'' comparison, identical dose calculation grid and dose-volume histogram calculator were used. Very good agreement was obtained for most of the cases, with no significant differences between the DVHs obtained from both calculations. However, deviations of up to 4% for the dose received by 95% of the target volume were found for the small lung tumors. Therefore, the approximations in the C/S algorithm slightly influence the accuracy in small lung tumors even though the C/S algorithm of the tomotherapy system shows very good overall behavior.

  4. Physical properties of the OMC-2 and OMC-3 cores from CS and C(18)O observations

    NASA Technical Reports Server (NTRS)

    Castets, A.; Langer, W. D.

    1995-01-01

    We have investigated the properties of the OMC-2 and OMC-3 cores in the Orion giant molecular cloud using high spatial spectral resolution observations of several transitions of the (13)CO, C(18)O, C(S-32) and C(S-34) molecules taken with the SEST telescope. The OMC-2 core consists of one clump (22 solar mass) with a radius of 0.11 pc surrounded by a cluster of 11 discrete infrared sources. The H2 column density and volume density in the center of this clump are 2 x 10(exp 22)/sq cm and 9 x 10(exp 5)/cu cm respectively. From a comparison between physical parameters derived from C(18)O and C(S-32) observations we conclude that the molecular envelope around the core has been completely removed by these sources and that only the very dense gas is left. OMC-3 shows a more complex elongated structure in C(18)O and CS than OMC-2. The C(S-32) and C(S-34) maps show that the denser region can be separated into at least sub-cores of roughly equal sizes (radius approximately equals 0.13 pc), with n(H2) = 6 x 10(exp 5)/cu cm, and a mass of 10 solar mass (from C(S-32)). The very different masses obtained for the central core from C(18)O and C(S-32) (55 and 12 solar mass respectively) indicate that a massive envelope is still present around the very dense sub-cores. We report the first detection of several molecular outflows in OMC-3. The presence of an IRAS source and the first detection of these outflows confirm that star formation is going on in OMC-3. Based on the different physical properties of these regions compared with OMC-1, OMC-2 appears to be in an intermediate evolutionary stage between OMC-1 and OMC-3.

  5. Structures and phase relations of aluminum-substituted calcium silicate hydrate

    SciTech Connect

    Kwan, S.; LaRosa-Thompson, J.; Grutzeck, M.W.

    1996-04-01

    The structures of aluminum-substituted calcium silicate hydrate (C-S-H) forming in a series of aqueous suspensions formulated with colloidal silica, reactive alumina, and lime and aged for 1 year have been studied using {sup 29}Si and {sup 27}Al magic angle spinning nuclear magnetic resonance spectroscopy (with and without cross polarization (CP)), solution pH, electron microscopy, and X-ray diffraction. As in earlier work dealing with the nature of C-S-H in the system CaO-SiO{sub 2}-H{sub 2}O, two aluminum-substituted C-S-H phases, having distinctly different anionic structures on the atomic level (Q{sub 2} versus Q{sub 1}Q{sub 2}), were found to extend into the system CaO-Al{sub 2}O{sub 3}-SiO{sub 2}-H{sub 2}O. X-ray diffraction patterns of the two aluminum-containing C-S-H phases are nearly identical, suggesting that their intermediate-range order is very similar, but MASNMR spectra show that these two phases have markedly different silicate structures on the atomic-level scale. Both C-S-H structures can accommodate approximately 5 mol% of Al{sub 2}O{sub 3} in tetrahedral and possibly octahedral coordination as well.

  6. Protocols for the selective cleavage of carbon-sulfur bonds in coal. Quarterly report, September 1, 1991--November 30, 1991

    SciTech Connect

    Bausch, M.

    1991-12-31

    Removal of the organic sulfur in coal constitutes one of the major challenges facing fossil fuel scientists today. A cost--effective of desulfurizing Illinois coal is non-existent at the present time. Research in our group aims to develop a simple protocol for sulfur removal by gaining understanding of how various additives can enhance the rates of C-S bond cleavage in Illinois coal and coal model compounds, relative to fragmentation of the coal macromolecule via C-C, C-O, and C-N bond cleavage. During this funding period, we plan to carry out examinations of: (a) the effects of various reaction conditions on radical-initiated and Lewis acid-catalyzed C-S bond cleavages; (b) the effects of caustic impregnation and subsequent alcoholic reflux on C-S bond cleavage strategies; (c) the reactions of coal model compounds with electron-deficient substrates; (d) examinations of photooxidative C-S bond cleavage reactions; (e) the effects of moderate (300--400{degrees}C) temperatures and pressures as well as ultrasonic radiation on (a) - (c). Also planned are differential scanning calorimetric (DSC) examinations of selected C-S bond cleavage protocols, including those on Illinois coals that possess varying amounts of organic and inorganic sulfur.

  7. Protocols for the selective cleavage of carbon-sulfur bonds in coal

    SciTech Connect

    Bausch, M.

    1991-01-01

    Removal of the organic sulfur in coal constitutes one of the major challenges facing fossil fuel scientists today. A cost--effective of desulfurizing Illinois coal is non-existent at the present time. Research in our group aims to develop a simple protocol for sulfur removal by gaining understanding of how various additives can enhance the rates of C-S bond cleavage in Illinois coal and coal model compounds, relative to fragmentation of the coal macromolecule via C-C, C-O, and C-N bond cleavage. During this funding period, we plan to carry out examinations of: (a) the effects of various reaction conditions on radical-initiated and Lewis acid-catalyzed C-S bond cleavages; (b) the effects of caustic impregnation and subsequent alcoholic reflux on C-S bond cleavage strategies; (c) the reactions of coal model compounds with electron-deficient substrates; (d) examinations of photooxidative C-S bond cleavage reactions; (e) the effects of moderate (300--400{degrees}C) temperatures and pressures as well as ultrasonic radiation on (a) - (c). Also planned are differential scanning calorimetric (DSC) examinations of selected C-S bond cleavage protocols, including those on Illinois coals that possess varying amounts of organic and inorganic sulfur.

  8. Elastic properties of swollen polyelectrolyte gels in aqueous salt solutions.

    PubMed

    Sasaki, Shigeo

    2006-03-01

    The elastic relaxation responding to a uniaxially stretched poly(acrylic acid) rodlike gel in the aqueous NaCl solution was investigated. The relaxation elucidated the shear (mu) and bulk (K) moduli and the frictional coefficients (sigma) of the fully ionized gel at pH above 9 as functions of the degree of swelling, which was controlled by the NaCl concentration (C(S)) of the solution. Two gels, cross-linked chains of which consist of 500 (GelA500) and 50 (GelA50) monomeric units, were examined to investigate the effect of the chain length on the elastic behavior. The moduli of GelA500 increased with swelling at C(S) below 100 mM and decreased at C(S) above it. The mu values of both gels can be characterized by the power function of gel diameter, d as mu proportional, variantd(beta). The beta values being -1 at C(S) above 100 mM transitionally changed to 1.2 at C(S) about 100 mM. That is, the dimensionality of space for the chains to distribute, n(dim) [= (beta+5)/(beta+2) according to the conventional theory [Sasaki et al., J. Chem. Phys. 102, 5694 (1995)

  9. Structure and phase investigations on crystallization of 11 A tobermorite in lime sand pellets

    SciTech Connect

    Hartmann, A. . E-mail: a.hartmann@tudelft.nl; Buhl, J.-Ch.; Breugel, K. van

    2007-01-15

    The present work examines the crystallization behaviour of 11 A tobermorite and its dependence on the reactivity of different silica sources (quartz sand, grain-size {<=} 0.30 mm; quartz powder, grain-size {<=} 0.08 mm; inflated clay sand, grain-size {<=} 0.50 mm and raw perlite, grain-size {<=} 1 mm). The influence of different C/S ratios (calcium/silica ratio: 0.53, 0.83) was also investigated. For simulation of the industrial production process of lime sand products, a synthesis of lime sand pellets was carried out with a hydrothermal treatment (T = 200 deg. C, t = 40.5 h). The C-S-H phases were characterized by ESEM, EDX and X-ray powder diffraction. The investigations revealed that the grain-size, C/S ratio and porosity of the silica sources influence the formation of 11 A tobermorite. A formation of 11 A tobermorite using inflated clay sand with a grain-size {<=} 0.50 mm and a high porosity was only found with a C/S ratio of 0.53. This indicates a negative influence of an increase of lime content inside the synthesis mixture for tobermorite crystallization. Besides, a formation of xonotlite inside big pores of the lime sand pellet with inflated clay sand could be observed. The formation of portlandite and calcite was detected in all samples. The amount of calcite increased with the grain-size and with a higher C/S ratio.

  10. Neural control of playing a reversed piano: empirical evidence for an unusual cortical organization of musical functions.

    PubMed

    Jäncke, Lutz; Baumann, Simon; Koeneke, Susan; Meyer, Martin; Laeng, Bruno; Peters, Michael; Lutz, Kai

    2006-03-20

    Using functional magnetic imaging techniques and neuropsychological tests, we studied a young male musician (C.S.) who performs at a professional level both on a regular piano keyboard and on a reverse keyboard (reversed right to left). The participant was left-handed, had left dominance for language but, remarkably, right dominance for the control of piano playing on both keyboards. With respect to music perception, C.S. showed left-sided activation dominance within the left superior temporal sulcus, which is normally associated with higher order auditory processing and right-sided activations in the secondary sensory cortex extending into the supramarginal gyrus. We suggest that C.S.'s pattern of functional asymmetry, characterized by audio-motor control using a right-sided network, could be a factor in his exceptional piano-playing ability on both the standard and reversed keyboard. PMID:16514374

  11. Laser heating and detection of bilayer microcantilevers for non-contact thermodynamic measurements

    NASA Astrophysics Data System (ADS)

    Burke, Brian G.; LaVan, David A.

    2013-01-01

    We describe a method for optical detection (frequency and position) and heating of bilayer microcantilevers (BMCs) to high temperatures at fast heating rates (106°C/s to 109°C/s) for non-contact thermodynamic measurements of small quantities of materials in the femtogram range. The current experimental apparatus with a 2 μm × 10 μm BMC achieves a deflection sensitivity of 0.1 Å, heating rate of 3.0 × 106°C/s, and heat sensitivity of 18 pJ in a 3 kHz bandwidth in air. By measuring the resonant frequency shift after sample loading, we achieve a mass resolution of 2.67 fg.

  12. Grain Boundary Segregation Behavior of Boron in Low-Alloy Steel

    NASA Astrophysics Data System (ADS)

    Shigesato, Genichi; Fujishiro, Taishi; Hara, Takuya

    2014-04-01

    The boron concentration profiles around prior austenite grain boundaries in Fe-0.05C-0.5Mo-0.001B (mass pct) are examined using aberration-corrected STEM-EELS. In order to obtain the precise distribution of boron around the boundaries, tilt series measurements with thin specimens (<30 nm) are performed and the EEL spectra are analyzed by principal component analysis (PCA) and multivariate curve resolution (MCR). The boron concentration profile changes with the cooling rate from the solid solution temperature. The concentration at grain boundaries is maximized at a medium rate (30 °C/s), where the concentration reaches 8 at. pct, and it decreases at a larger (250 °C/s) or smaller (5 °C/s) rate. On the other hand, the boron distribution becomes wider as the cooling rate becomes smaller. The current results suggest that the boron segregation in the alloy is formed by the "non-equilibrium segregation mechanism."

  13. Chemical structure of cement aged at normal and elevated temperatures and pressures, Part II: Low permeability class G oilwell cement

    SciTech Connect

    Le Saout, Gwenn . E-mail: gwenn.lesaout@epfl.ch; Lecolier, Eric; Rivereau, Alain; Zanni, Helene

    2006-03-15

    Recently, Low Permeability Cement formulation has been developed for oilwell cementing. Therefore, it is important to understand the physical and chemical processes causing cement degradation in the downhole environment. In this study, we have characterised a Low Permeability Class G oilwell Cement immersed for one year in brine at T = 293 K, p = 10{sup 5} Pa and T = 353 K, p = 7 x 10{sup 6} Pa using {sup 29}Si, {sup 27}Al NMR and XRD techniques. Elevated temperature and pressure conditions increase the rate of the pozzolanic reaction and have significant effects on the polymerisation of C-S-H and on the incorporation of Al in the C-S-H structure. Leaching resulted in the formation of calcite and a more polymerised C-S-H with the appearance of tobermorite in the sample cured at elevated temperature and pressure.

  14. Retention of alkali ions by hydrated low-pH cements: Mechanism and Na{sup +}/K{sup +} selectivity

    SciTech Connect

    Bach, T.T.H.; Chabas, E.; Cau Dit Coumes, C.; Frizon, F.

    2013-09-15

    Low-pH cements, also referred to as low-alkalinity cements, can be designed by replacing significant amounts of Portland cement by pozzolanic materials. Their pore solution is characterized by a pH near 11, and an alkali concentration much lower than that of Portland cement. This work investigates the retention of sodium and potassium by a hydrated low-pH cement comprising 60% Portland cement and 40% silica fume. It is shown that sorption of potassium is higher than that of sodium and mainly results from counterion charge balancing of the C-S-H negative surface charge. To explain the greater retention of potassium compared to sodium, it is postulated that potassium, unlike sodium, may enter the interlayer of C-S-H to compensate the negative charges in the interlayer, in addition to the external surfaces. This assumption is supported by structural characterization of C-S-H using X-ray diffraction.

  15. In situ time-resolved X-ray diffraction of tobermorite formation in autoclaved aerated concrete: Influence of silica source reactivity and Al addition

    SciTech Connect

    Matsui, Kunio; Kikuma, Jun; Tsunashima, Masamichi; Ishikawa, Tetsuji; Matsuno, Shin-ya; Ogawa, Akihiro; Sato, Masugu

    2011-05-15

    The hydrothermal formation of tobermorite during the processing of autoclaved aerated concrete was investigated by in situ X-ray diffraction (XRD) analysis. High-energy X-rays from a synchrotron radiation source in combination with a newly developed autoclave cell and a photon-counting pixel array detector were used. To investigate the effects of the silica source, reactive quartz from chert and less-reactive quartz from quartz sand were used as starting materials. The effect of Al addition on tobermorite formation was also studied. In all cases, C-S-H, hydroxylellestadite and katoite were clearly observed as intermediates. Acceleration of tobermorite formation by Al addition was clearly observed. However, Al addition did not affect the dissolution rate of quartz. Two pathways, via C-S-H and katoite, were also observed in the Al-containing system. These results suggest that the structure of initially formed C-S-H is important for the subsequent tobermorite formation reactions.

  16. Interaction grand potential between calcium-silicate-hydrate nanoparticles at the molecular level

    NASA Astrophysics Data System (ADS)

    Bonnaud, Patrick A.; Labbez, Christophe; Miura, Ryuji; Suzuki, Ai; Miyamoto, Naoto; Hatakeyama, Nozomu; Miyamoto, Akira; van Vliet, Krystyn J.

    2016-02-01

    Calcium-silicate-hydrate (or C-S-H), an inosilicate, is the major binding phase in cement pastes and concretes and a porous hydrated material made up of a percolated and dense network of crystalline nanoparticles of a mean apparent spherical diameter of ~5 nm that are each stacks of multiple C-S-H layers. Interaction forces between these nanoparticles are at the origin of C-S-H chemical, physical, and mechanical properties at the meso- and macroscales. These particle interactions and the resulting properties may be affected significantly by nanoparticle density and environmental conditions such as the temperature, relative humidity, or concentration of chemical species in the bulk solution. In this study, we combined grand canonical Monte Carlo simulations and an extension of the mean force integration method to derive the pair potentials. This approach enables realistic simulation of the physical environment surrounding the C-S-H particles. We thus constructed the pair potentials for C-S-H nanoparticles of defined chemical stoichiometry at 10% relative humidity (RH), varying the relative crystallographic orientations at a constant particle density of ρpart ~ 2.21 mmol L-1. We found that cohesion between nanoparticles is affected strongly by both the aspect ratio and the crystallographic misorientation of interacting particles. This method and the findings underscore the importance of accounting for relative dimensions and orientation among C-S-H nanoparticles in descriptions of physical and simulated multiparticle aggregates or mesoscale systems.Calcium-silicate-hydrate (or C-S-H), an inosilicate, is the major binding phase in cement pastes and concretes and a porous hydrated material made up of a percolated and dense network of crystalline nanoparticles of a mean apparent spherical diameter of ~5 nm that are each stacks of multiple C-S-H layers. Interaction forces between these nanoparticles are at the origin of C-S-H chemical, physical, and mechanical

  17. Drugs Modulate Interactions between the First Nucleotide-Binding Domain and the Fourth Cytoplasmic Loop of Human P-Glycoprotein.

    PubMed

    Loo, Tip W; Clarke, David M

    2016-05-24

    Drug substrates stimulate ATPase activity of the P-glycoprotein (P-gp) ATP-binding cassette drug pump by an unknown mechanism. Cross-linking analysis was performed to test if drug substrates stimulate P-gp ATPase activity by altering cross-talk at the first transmission interface linking the drug-binding [intracellular loop 4 (S909C)] and first nucleotide-binding domains [NBD1 (V472C or L443C)]. In the absence of lipid (inactive P-gp), only V472C/S909C showed cross-linking. Drugs blocked V472C/S909C cross-linking. In the presence of lipids (active P-gp), drug substrates promoted only L443C/S909C cross-linking. This suggests that drug substrates stimulate ATPase activity through a conformational change that shifts Ser909 away from Val472 and toward Leu443. PMID:27159830

  18. Model for the developing microstructure in Portland cement pastes

    SciTech Connect

    Jennings, H.M.; Tennis, P.D. )

    1994-12-01

    A method is proposed for quantitatively predicting the volume of the major phases in hydrated cement pastes as a function of (1) the composition of the cement, (2) the degree of reaction, and (3) the initial water: cement ratio. This procedure is then used to develop a quantitative model for the surface area and volume of porosity that is accessible to nitrogen in calcium silicate hydrate (C-S-H). Published values for surface areas and volume of pores are compared with the predictions made by the model. An implication of the model is that there are two types of C-S-H, or perhaps regions within the C-S-H: one that nitrogen can penetrate and one that it cannot.

  19. Stability of the aqueous suspensions of nanotubes in the presence of nonionic surfactant.

    PubMed

    Lisunova, Milana O; Lebovka, Nikolai I; Melezhyk, Olexander V; Boiko, Yurie P

    2006-07-15

    Stability of aqueous suspensions of multiwalled carbon nanotubes (MWNTs) and their percolation behavior are investigated. Nanotubes of aqueous suspensions show a strong tendency to aggregation and networking into electroconductive clusters. The percolation threshold of the electrical conductivity is rather low and of order phi approximately 0.01 (where phi is the volume fraction), which can be explained by the high aspect ratio of MWNTs. Strong influence of the nonionic surfactant Triton X-305 on the colloidal stability of aqueous suspensions of MWNTs is observed. Addition of surfactant exerts a stabilizing effect at surfactant concentration C(s) proportional to the weight concentration C of MWNTs, C(s) approximately C mol/dm3. The transient behavior of electrical conductivity in the aqueous suspensions is explained by fractal aggregation processes. The fractal dimension is shown to be sensitive to the surfactant concentration C(s). PMID:16600279

  20. Obstructed Defecation Syndrome After Delivery Trauma

    PubMed Central

    Mehrvarz, Shaban; Towliat, Seyed Mohsem; Mohebbi, Hassan Ali; Heydari, Soleyman; Farahani, Mahdi; Rasouli, Hamid Reza

    2015-01-01

    Background: Obstructed defecation syndrome (ODS) occurs in about 7% of adults; it seems that the etiology of pelvic floor disorders is multifactorial. Pregnancy and childbirth damage to the pelvic nerve and muscles are proposed causes for this condition. The precise role of vaginal delivery (VD) is not clearly defined, although in recent studies association of pelvic floor disorder with Operative vaginal delivery and episiotomy has been proposed. Objectives: In this prospective study, we assessed the outcome of stapled transanal rectal resection (STARR) in females with one of the two modes of delivery (VD or caesarean section (C/S). Patients and Methods: We used Longo’s ODS score for the assessment of the severity of pelvic floor malfunction. Stapled Trans Anal Rectal Resection (STARR) procedure was performed using two circular staplers. Follow-up was done 12 months after the discharge. To assess the role of episiotomy in patient with VD, we divided them into two subgroups; females who had VD with episiotomy (Vd + epi) and females who had VD alone. Data were analyzed using SPSS version 20 software. P values less than 0.05 were considered statistically significant. Results: In 30 consecutive females undergoing STARR for the treatment of ODS, who enrolled in this prospective study, 19 (63.3%) had Vaginal Delivery VD and 11 (36.7%) had Cesarean Section (C/S). The ODS score before the surgery was higher in females who had C/S, although there was no significant difference between VD and C/S groups in terms of the percentage of the ODS score improvement after the STARR surgery. Conclusions: Higher ODS score in females who had C/S showed that C/S could not protect the pelvic organ from pregnancy and delivery trauma. It seems that episiotomy has a protective effect during VD; it can reduce the severity of trauma in pelvic organs during childbearing. PMID:26839863

  1. P-glycoprotein ATPase activity requires lipids to activate a switch at the first transmission interface.

    PubMed

    Loo, Tip W; Clarke, David M

    2016-04-01

    P-glycoprotein (P-gp) is an ABC (ATP-Binding Cassette) drug pump. A common feature of ABC proteins is that they are organized into two wings. Each wing contains a transmembrane domain (TMD) and a nucleotide-binding domain (NBD). Drug substrates and ATP bind at the interface between the TMDs and NBDs, respectively. Drug transport involves ATP-dependent conformational changes between inward- (open, NBDs far apart) and outward-facing (closed, NBDs close together) conformations. P-gps crystallized in the presence of detergent show an open structure. Human P-gp is inactive in detergent but basal ATPase activity is restored upon addition of lipids. The lipids might cause closure of the wings to bring the NBDs close together to allow ATP hydrolysis. We show however, that cross-linking the wings together did not activate ATPase activity when lipids were absent suggesting that lipids may induce other structural changes required for ATPase activity. We then tested the effect of lipids on disulfide cross-linking of mutants at the first transmission interface between intracellular loop 4 (TMD2) and NBD1. Mutants L443C/S909C and L443C/R905C but not G471C/S909C and V472C/S909C were cross-linked with oxidant when in membranes. The mutants were then purified and cross-linked with or without lipids. Mutants G471C/S909C and V472C/S909C cross-linked only in the absence of lipids whereas mutants L443C/S909C and L443C/R905C were cross-linked only in the presence of lipids. The results suggest that lipids activate a switch at the first transmission interface and that the structure of P-gp is different in detergents and lipids. PMID:26944019

  2. Mesoscale texture of cement hydrates.

    PubMed

    Ioannidou, Katerina; Krakowiak, Konrad J; Bauchy, Mathieu; Hoover, Christian G; Masoero, Enrico; Yip, Sidney; Ulm, Franz-Josef; Levitz, Pierre; Pellenq, Roland J-M; Del Gado, Emanuela

    2016-02-23

    Strength and other mechanical properties of cement and concrete rely upon the formation of calcium-silicate-hydrates (C-S-H) during cement hydration. Controlling structure and properties of the C-S-H phase is a challenge, due to the complexity of this hydration product and of the mechanisms that drive its precipitation from the ionic solution upon dissolution of cement grains in water. Departing from traditional models mostly focused on length scales above the micrometer, recent research addressed the molecular structure of C-S-H. However, small-angle neutron scattering, electron-microscopy imaging, and nanoindentation experiments suggest that its mesoscale organization, extending over hundreds of nanometers, may be more important. Here we unveil the C-S-H mesoscale texture, a crucial step to connect the fundamental scales to the macroscale of engineering properties. We use simulations that combine information of the nanoscale building units of C-S-H and their effective interactions, obtained from atomistic simulations and experiments, into a statistical physics framework for aggregating nanoparticles. We compute small-angle scattering intensities, pore size distributions, specific surface area, local densities, indentation modulus, and hardness of the material, providing quantitative understanding of different experimental investigations. Our results provide insight into how the heterogeneities developed during the early stages of hydration persist in the structure of C-S-H and impact the mechanical performance of the hardened cement paste. Unraveling such links in cement hydrates can be groundbreaking and controlling them can be the key to smarter mix designs of cementitious materials. PMID:26858450

  3. Containment and surveillance -- A principal IAEA safeguards measure

    SciTech Connect

    Drayer, D.D.; Dupree, S.A.; Sonnier, C.S.

    1997-12-31

    The growth of the safeguards inspectorate of the Agency, spanning more than 40 years, has produced a variety of interesting subjects (legal, technical, political, etc.) for recollection, discussion, and study. Although the Agency was established in 1957, the first practical inspections did not occur until the early 1960s. In the early inspections, thee was little C/S equipment available, and no optical surveillance was used. However, by the third decade of the IAEA, the 1980s, many technology advances were made, and the level of C/S equipment activities increased. By the late 1980s, some 200 Twin Minolta film camera systems were deployed by the Agency for safeguards use. At the present time, the Agency is evaluating and beginning to implement remote monitoring as part of the Strengthened Safeguards System. However, adoption of remote monitoring by international agencies cannot occur rapidly because of the many technical and policy issues associated with this activity. A glimpse into the future indicates that an important element of safeguards instrumentation will be the merging of C/S and NDA equipment into integrated systems. The use of modern interior area monitors in International Safeguards also offers a great potential for advancing C/S measures. The research in microsensors is in its infancy, and the opportunities for their reducing the cost, increasing the life time, and increasing the reliability of sensors for safeguards applications are manifold. A period may be approaching in which the terminology of C/S will no longer have its original meaning, as integrated systems combining NDA instruments and C/S instruments are already in use and are expected to be the norm in the near future.

  4. A multi-technique investigation of the nanoporosity of cement paste

    SciTech Connect

    Jennings, Hamlin M. . E-mail: h-jennings@northwestern.edu; Thomas, Jeffrey J. . E-mail: jthomas@northwestern.edu; Gevrenov, Julia S.; Constantinides, Georgios; Ulm, Franz-Josef

    2007-03-15

    The nanometer-scale structure of cement paste, which is dominated by the colloidal-scale porosity within the C-S-H gel phase, has a controlling effect on concrete properties but is difficult to study due to its delicate structure and lack of long-range order. Here we present results from three experimental techniques that are particularly suited to analyzing disordered nanoporous materials: small-angle neutron scattering (SANS), weight and length changes during equilibrium drying, and nanoindentation. Particular attention is paid to differences between pastes of different ages and cured at different temperatures. The SANS and equilibrium drying results indicate that hydration of cement paste at 20 deg. C forms a low-density (LD) C-S-H gel structure with a range of gel pore sizes and a relatively low packing fraction of solid particles. This fine structure may persist indefinitely under saturated conditions. However, if the paste is dried or is cured at elevated temperatures (60 deg. C or greater) the structure collapses toward a denser (less porous) and more stable configuration with fewer large gel pores, resulting in a greater amount of capillary porosity. Nanoindentation measurements of pastes cured at different temperatures demonstrate in all cases the existence of two C-S-H structures with different characteristic values of the indentation modulus. The average value of the modulus of the LD C-S-H is the same for all pastes tested to date, and a micromechanical analysis indicates that this value corresponds to the denser and more stable configuration of LD C-S-H. The experimental results presented here are interpreted in terms of a previously proposed quantitative 'colloid' model of C-S-H gel, resulting in an improved understanding of the microstructural changes associated with drying and heat curing.

  5. DNA Three Way Junction Core Decorated with Amino Acids-Like Residues-Synthesis and Characterization.

    PubMed

    Addamiano, Claudia; Gerland, Béatrice; Payrastre, Corinne; Escudier, Jean-Marc

    2016-01-01

    Construction and physico-chemical behavior of DNA three way junction (3WJ) functionalized by protein-like residues (imidazole, alcohol and carboxylic acid) at unpaired positions at the core is described. One 5'-C(S)-propargyl-thymidine nucleotide was specifically incorporated on each strand to react through a post synthetic CuACC reaction with either protected imidazolyl-, hydroxyl- or carboxyl-azide. Structural impacts of 5'-C(S)-functionalization were investigated to evaluate how 3WJ flexibility/stability is affected. PMID:27563857

  6. High performance fiber-coupled NbTiN superconducting nanowire single photon detectors with Gifford-McMahon cryocooler.

    PubMed

    Miki, Shigehito; Yamashita, Taro; Terai, Hirotaka; Wang, Zhen

    2013-04-22

    We present high performance fiber-coupled niobium titanium nitride superconducting nanowire single photon detectors fabricated on thermally oxidized silicon substrates. The best device showed a system detection efficiency (DE) of 74%, dark count rate of 100 c/s, and full width at half maximum timing jitter of 68 ps under a bias current of 18.0 μA with a practical Gifford-McMahon cryocooler system. We also introduced six detectors into the cryocooler and confirmed that the system DE of all detectors was higher than 67% at the dark count rate of 100 c/s. PMID:23609728

  7. Knowledge, attitude and practices for design for safety: A study on civil & structural engineers.

    PubMed

    Goh, Yang Miang; Chua, Sijie

    2016-08-01

    Design for safety (DfS) (also known as prevention through design, safe design and Construction (Design and Management)) promotes early consideration of safety and health hazards during the design phase of a construction project. With early intervention, hazards can be more effectively eliminated or controlled leading to safer worksites and construction processes. DfS is practiced in many countries, including Australia, the UK, and Singapore. In Singapore, the Manpower Ministry enacted the DfS Regulations in July 2015, which will be enforced from August 2016 onwards. Due to the critical role of civil and structural (C&S) engineers during design and construction, the DfS knowledge, attitude and practices (KAP) of C&S engineers have significant impact on the successful implementation of DfS. Thus, this study aims to explore the DfS KAP of C&S engineers so as to guide further research in measuring and improving DfS KAP of designers. During the study, it was found that there is a lack of KAP studies in construction management. Therefore, this study also aims to provide useful lessons for future applications of the KAP framework in construction management research. A questionnaire was developed to assess the DfS KAP of C&S engineers. The responses provided by 43 C&S engineers were analyzed. In addition, interviews with experienced construction professionals were carried out to further understand perceptions of DfS and related issues. The results suggest that C&S engineers are supportive of DfS, but the level of DfS knowledge and practices need to be improved. More DfS guidelines and training should be made available to the engineers. To ensure that DfS can be implemented successfully, there is a need to study the contractual arrangements between clients and designers and the effectiveness of different implementation approaches for the DfS process. The questionnaire and findings in this study provided the foundation for a baseline survey with larger sample size, which is

  8. Manufacture of bulk superconducting YBa2Cu3O(7-delta) by a continuous process

    NASA Technical Reports Server (NTRS)

    Meng, R. L.; Kinalidis, C.; Sun, Y. Y.; Gao, L.; Tao, Y. K.

    1990-01-01

    The development of a continuous process for fabricating large bulk superconductors with a predetermined grain orientation is reported. A bar of the 123 compound with dimensions 5 x 0.5 x about 0.3 cm with excellent grain alignment has been fabricated continuously. The bulk 123 thus obtained has magnetically determined J(c)s of about 30,000 and 12,000 A/sq cm at 0 and 1 T, respectively, and transport J(c)s of 20,000, 11,000, and 7500 A-sq cm at 0, 0.54, and 0.83 T.

  9. Experiments with powdered CMN thermometers between 10 mK and 4K, and a comparison with an NBS SRM 768 fixed-point device

    SciTech Connect

    Fogle, W.E.; Hornung, E.W.; Mayberry, M.C.; Phillips, N.E.

    1981-08-01

    Comparison of a powdered CMN thermometer with an NBS fixed point device demonstrates an internal inconsistency in the T/sub c/'s assigned to the fixed point device. T/sub c/'s between 100 and 200 mK are in excellent agreement with a temperature scale interpolated between He vapor pressure temperatures and nuclear orientation temperatures, but there is a discrepancy of 8% at the 15 mK point. Evidence for different susceptibility-temperature relations for superficially similar CMN thermometers is also presented.

  10. INSAT-2A and 2B development mechanisms

    NASA Technical Reports Server (NTRS)

    Sathyanarayan, M. N.; Rao, M. Nageswara; Nataraju, B. S.; Viswanatha, N.; Chary, M. Laxmana; Balan, K. S.; Murthy, V. Sridhara; Aller, Raju; Kumar, H. N. Suresha

    1994-01-01

    The Indian National Satellite (INSAT) 2A and 2B have deployment mechanisms for deploying the solar array, two C/S band antenna reflectors and a coilable lattice boom with sail. The mechanisms have worked flawlessly on both satellites. The configuration details, precautions taken during the design phase, the test philosophy, and some of the critical analysis activities are discussed.

  11. Early age hydration and pozzolanic reaction in natural zeolite blended cements: Reaction kinetics and products by in situ synchrotron X-ray powder diffraction

    SciTech Connect

    Snellings, R.; Mertens, G.; Cizer, O.; Elsen, J.

    2010-12-15

    The in situ early-age hydration and pozzolanic reaction in cements blended with natural zeolites were investigated by time-resolved synchrotron X-ray powder diffraction with Rietveld quantitative phase analysis. Chabazite and Na-, K-, and Ca-exchanged clinoptilolite materials were mixed with Portland cement in a 3:7 weight ratio and hydrated in situ at 40 {sup o}C. The evolution of phase contents showed that the addition of natural zeolites accelerates the onset of C{sub 3}S hydration and precipitation of CH and AFt. Kinetic analysis of the consumption of C{sub 3}S indicates that the enveloping C-S-H layer is thinner and/or less dense in the presence of alkali-exchanged clinoptilolite pozzolans. The zeolite pozzolanic activity is interpreted to depend on the zeolite exchangeable cation content and on the crystallinity. The addition of natural zeolites alters the structural evolution of the C-S-H product. Longer silicate chains and a lower C/S ratio are deduced from the evolution of the C-S-H b-cell parameter.

  12. Camelina growing degree hour and base temperature requirements

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Oilseed crops show potential as biofuel feedstocks that can diversify spring wheat rotations in the northern Great Plains. Camelina is a relatively new oilseed crop, with limited emergence information available. A 70-day incubator study investigated the impact of temperature (0, 2, 4, and 16 °C), s...

  13. 6. DETAIL VIEW OF BRIDGE DATEPLATE WHICH READS '1930, WHITE ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    6. DETAIL VIEW OF BRIDGE DATEPLATE WHICH READS '1930, WHITE RIVER BRIDGE, ARKANSAS HIGHWAY COMMISSION, DWIGHT BLACKWOOD, CHAIRMAN, JUSTIN MATTHEWS, J. LAN WILLIAMS, J.S. PARKS, SAM J. WILSON, COMMISSIONERS, C.S. CHRISTIAN, STATE HIGHWAY ENGINEER, IRA HEDRICK, INC., CONSULTING ENGINEERS, PARHAM CONT. CO., CONTRACTOR' - Augusta Bridge, Spanning White River at Highway 64, Augusta, Woodruff County, AR

  14. CENTRAL DOPAMINE AND SEROTONIN TURNOVER IN SCHIZOPHRENIA

    PubMed Central

    Pandey, R.S.; Rao, B.S.S.; Subash, M.N.; Subba Krishna, D.K.; Srinivas, K.N.

    1987-01-01

    SUMMARY Comparison of C.S. F. H. V. A and 5-HIAA levels of 20 Schizophrenics and 9 non-schizophrenic controls revealed no statistically significant difference between HVA levels but the 5-HIAA levels were significantly less in Schizophrenics (p < 0.05) than in controls. The significance of these findings is discussed. PMID:21927240

  15. 32 CFR 246.3 - Definitions.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... STARS AND STRIPES (S&S) NEWSPAPER AND BUSINESS OPERATIONS § 246.3 Definitions. (a) Adverse Conditions... publisher of the Stars and Stripes produced by that organization. (c) S&S Management Action Group (MAG) and... issues. Neither the DoD S&S Steering Committee, nor the S&S MAG, involve themselves in Stars and...

  16. 32 CFR 246.3 - Definitions.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... STARS AND STRIPES (S&S) NEWSPAPER AND BUSINESS OPERATIONS § 246.3 Definitions. (a) Adverse Conditions... publisher of the Stars and Stripes produced by that organization. (c) S&S Management Action Group (MAG) and... issues. Neither the DoD S&S Steering Committee, nor the S&S MAG, involve themselves in Stars and...

  17. 32 CFR 246.3 - Definitions.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... STARS AND STRIPES (S&S) NEWSPAPER AND BUSINESS OPERATIONS § 246.3 Definitions. (a) Adverse Conditions... publisher of the Stars and Stripes produced by that organization. (c) S&S Management Action Group (MAG) and... issues. Neither the DoD S&S Steering Committee, nor the S&S MAG, involve themselves in Stars and...

  18. 32 CFR 246.3 - Definitions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... STARS AND STRIPES (S&S) NEWSPAPER AND BUSINESS OPERATIONS § 246.3 Definitions. (a) Adverse Conditions... publisher of the Stars and Stripes produced by that organization. (c) S&S Management Action Group (MAG) and... issues. Neither the DoD S&S Steering Committee, nor the S&S MAG, involve themselves in Stars and...

  19. 32 CFR 246.3 - Definitions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... STARS AND STRIPES (S&S) NEWSPAPER AND BUSINESS OPERATIONS § 246.3 Definitions. (a) Adverse Conditions... publisher of the Stars and Stripes produced by that organization. (c) S&S Management Action Group (MAG) and... issues. Neither the DoD S&S Steering Committee, nor the S&S MAG, involve themselves in Stars and...

  20. The Effects of Cooling Mode on Precipitation and Mechanical Properties of a Ti-Nb Microalloyed Steel

    NASA Astrophysics Data System (ADS)

    Hu, Zhangwei; Xu, Guang; Yang, Hailin; Zhang, Chen; Yu, Ru

    2014-12-01

    Laboratory experiments of a high-strength Ti-Nb microalloyed steel were conducted with two cooling modes, i.e., a large (35 °C s-1) cooling rate in the initial stage followed by slow (8.5 °C s-1) cooling rate (termed as FFC) and a slow (8.5 °C s-1) cooling rate in the initial stage followed by large (35 °C s-1) cooling rate (LFC) during cooling process. Based on the results of laboratory experiments, an industrial trial was performed with similar steel on a continuous hot strip production mill. The grain size in LFC sample (2.83 μm) is smaller than that in FFC sample (3.80 μm), and the volume fraction of precipitates in LFC sample (1.04%) is more than that in FFC sample (0.81%). Both results of laboratory experiments and industrial tests confirm that the strengthening effect of the LFC mode is much better than that of the FFC mode from the viewpoints of both fine-grain strengthening and precipitation strengthening. The present study provides a new approach to improve the property of microalloyed steels produced by continuous hot rolling technology.

  1. John Donne: A Collection of Critical Essays. Twentieth Century Views Series.

    ERIC Educational Resources Information Center

    Gardner, Helen, Ed.

    One of a series of works aimed at presenting contemporary opinion on major authors, this collection includes essays by Helen Gardner, George Saintsbury, Herbert J. C. Grierson, Pierre Legouis, William Empson, Mario Praz, J. E. V. Crofts, C. S. Lewis, Cleanth Brooks, J. B. Leishman, Evelyn M. Simpson, Louis L. Martz, and A. J. Smith--all dealing…

  2. Codes and standards research, development and demonstration roadmap

    SciTech Connect

    None, None

    2008-07-22

    C&S RD&D Roadmap - 2008: This Roadmap is a guide to the Research, Development & Demonstration activities that will provide data required for Standards Development Organizations (SDOs) to develop performance-based codes and standards for a commercial hydrogen fueled transportation sector in the U.S.

  3. Michigan Youth Farm Stand Project: Facets of Participant Motivation

    ERIC Educational Resources Information Center

    Rivera-Caudill, Jennifer; Brander, Ashley A.

    2008-01-01

    The purpose of the exploratory study was to understand what youth motivations in the Michigan Youth Farm Stand Project (YFSP) offered by the C.S Mott Group for Sustainable Food Systems at Michigan State University. The qualitative study included interviews and observations to explore the motivations of youth participants. An opportunity to earn…

  4. 75 FR 28672 - Bureau of International Security and Nonproliferation; Lifting of Nonproliferation Measures...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-05-21

    ... January 8, 1999 (see 64 FR 2935). Dated: May 17, 2010. C.S. Eliot Kang, Acting Assistant Secretary of... of International Security and Nonproliferation; Lifting of Nonproliferation Measures Against Two... measures on two Russian entities. DATES: Effective Date: May 21, 2010. FOR FURTHER INFORMATION...

  5. 75 FR 5836 - Lifting of Nonproliferation Measures Against One Russian Entity

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-02-04

    ... July 30, 1998 (see 63 FR 42089). Dated: January 29, 2010. C.S. Eliot Kang, Acting Assistant Secretary... of Nonproliferation Measures Against One Russian Entity AGENCY: Department of State. ACTION: Notice..., 1994, as amended, to remove nonproliferation measures on one Russian entity. DATES: Effective...

  6. Jane Austen: A Collection of Critical Essays. Twentieth Century Views Series.

    ERIC Educational Resources Information Center

    Watt, Ian, Ed.

    One of a series of works aimed at presenting contemporary critical opinion on major authors, this collection includes essays by Virginia Woolf, C. S. Lewis, Edmund Wilson, Ian Watt, Alan D. McKillop, Reuben A. Brower, Marvin Mudrick, Mark Schorer, Arnold Kettle, Lionel Trilling, Kingsley Amis, Andrew H. Wright, Donald J. Greene, and D. W.…

  7. Aggregates of Isotactic Poly(methacrylic acid) Chains in Aqueous CsCl Solutions: a Static and Dynamic Light Scattering Study.

    PubMed

    Hočevar, Katarina; Sitar, Simona; Kogej, Ksenija

    2015-01-01

    Properties of isotactic polymethacrylic acid, iPMA, chains were studied at 25°C in aqueous solutions at various CsCl concentrations, c(s) (= 0.05-0.20 M), in dependence on degree of neutralization of the polyion's carboxyl groups, α(N), using static, SLS, and dynamic light scattering, DLS, measurements. It was demonstrated that iPMA chains with α(N) somewhat above the solubility limit of iPMA in aqueous solutions (in the present case at α(N) ≈ 0.27) are strongly aggregated. The size of the aggregates increases with increasing c(s), whereas the shape parameter, ρ, is approximately constant (ρ ≈ 0.6), irrespective of c(s). The low ρ value suggests that the aggregates have characteristics of microgel particles with a dense core surrounded by a less dense corona. The diffusion of iPMA chains was investigated also at higher α(N), up to α(N) = 1. The polyion slow mode arising from electrostatic interactions between charged chains was observed for α(N) exceeding the value 0.27 even at the highest c(s) (= 0.20 M). The diffusion coefficients for the show mode were nearly independent of α(N) and cs at the studied polymer concentration. PMID:26454588

  8. China-U.S. Conference on Education. Collected Papers. (Beijing, People's Republic of China, July 9-13, 1997).

    ERIC Educational Resources Information Center

    Walz, Garry R.

    This book contains papers presented by educators during the China-U.S. Conference on Education in July, 1997. Only papers prepared by American authors were received and included in this collection. Chapters included are (1) "Art, Education, and Community: Arts Genesis, Inc." (C. S. Kestler); (2) "Applications of Portfolio Assessment in a Teaching…

  9. Shakespeare, The Tragedies: A collection of Critical Essays. Twentieth Century Views Series.

    ERIC Educational Resources Information Center

    Harbage, Alfred, Ed.

    One of a series of works aimed at presenting contemporary critical opinion on major authors, this collection includes essays by Alfred Harbage, H. B. Charlton, Willard Farnham, H. T. Price, Donald A. Stauffer, Brents Stirling, Maynard Mack, Helen Gardner, C. S. Lewis, Alvin Kernan, Bernard Spivack, L. C. Knights, Francis Fergusson, G. Wilson…

  10. 20 CFR 645.212 - Who may be served under the general eligibility and noncustodial parent eligibility (primary...

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... individuals (as well as children of noncustodial parents) exempted from the time limits due to hardship under...); or (c) (S)he is a noncustodial parent of a minor child if: (1) The noncustodial parent is: (i... minor child, or the custodial parent of the minor child, meets the long-term recipient of...