WorldWideScience

Sample records for synthesis polyolefin carbocyclizations

  1. Sulfur ylides in the synthesis of heterocyclic and carbocyclic compounds

    International Nuclear Information System (INIS)

    Lakeev, Sergei N; Maydanova, Irina O; Galin, Fanur Z; Tolstikov, Genrikh A

    2001-01-01

    Data on the use of sulfonium ylides in the synthesis of carbocyclic and heterocyclic compounds published over the last 15 years are analysed, systematised and generalised. The bibliography includes 139 references.

  2. Synthesis and Antiviral Activity of Novel 4'-Branched Carbocyclic C-Nucleoside

    Energy Technology Data Exchange (ETDEWEB)

    Jin, Ying Lan; Hong, Joon Hee [Chosun University, Gwangju (Korea, Republic of)

    2005-09-15

    C-Nucleosides have received considerable attention due not only to the chemical stability but also to the interesting biological activities of naturally occurring compounds such as showdomycin, formycins, oxazinomycin, etc. Also, several biologically active synthetic C-nucleosides such as pseudoisocytidine, thiazofurin, and 9-deazaadenosine have been reported. Carbocyclic nucleosides are another class of metabolically stable nucleosides in which a methylene group replaces the oxygen in the furan ring of the natural nucleosides. Another interesting feature of carbocyclic nucleosides is that a number of carbocyclic adenosine analogues are assumed to exert their antiviral action via the inhibition of S-adenosyl-homocysteine hydrolase. Moreover, this mechanism might be exploited in a combination therapy in association with the nucleosides with a different mechanism of action. On the basis of these interesting chemical and biological properties of C-nucleosides and carbocyclic nucleosides, it was of interest to synthesize hybrid nucleosides, carbocyclic C-nucleosides. Although some carbocyclic and C-nucleosides are naturally occurring, so far no natural carbocyclic C-nucleosides have been reported. The history of synthesis of carbocyclic C-nucleosides dates back to the 1960s. Despite the long history of carbocyclic C-nucleosides, only a few carbocyclic C-nucleosides have been synthesized, probably due to the synthetic difficulties of these nucleosides. Herein, we would like to report the synthesis procedure of a novel 4'-branched carbocyclic C-nucleoside.

  3. Synthesis of a Novel Carbocyclic Analog of Bredinin

    Directory of Open Access Journals (Sweden)

    Vasu Nair

    2013-09-01

    Full Text Available The natural nucleoside antibiotic, bredinin, exhibits antiviral and other biological activities. While various nucleosides related to bredinin have been synthesized, its carbocyclic analog has remained unknown. Synthesis of this heretofore unknown analog of bredinin is described. The key precursor, (3aS,4R,6R,6aR-6-((methoxy-methoxymethyl-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-amine (5, was prepared from the commercially available compound, (1R,4S-2-azabicyclo[2.2.1] hept-5-en-3-one (4. Our initial approach used intermediate 6, derived in three transformations from 5, for the key photolytic step to produce the desired ring-opened precursor to the target compound. This photochemical transformation was unsuccessful. However, an appropriately protected and related precursor was synthesized from 5 through the following side-chain functional group transformations: elaboration of the amino group through malonyl ester formation, oximation at the central carbon, conversion of ester to amide and catalytic reduction of the oxime group. This precursor, on treatment with triethylorthoformate and catalytic acetic acid in ethanol, underwent cyclization to produce the desired 4-carbamoyl-imidazolium-5-olate ring. Deprotection of the latter product proceeded smoothly to give the carbocyclic analog of bredinin. This target molecule exhibits antiviral activity, albeit low, against a number of RNA viruses. Further biological evaluations are in progress.

  4. Revaluation of biomass-derived furfuryl alcohol derivatives for the synthesis of carbocyclic nucleoside phosphonate analogues

    OpenAIRE

    Sidi Mohamed, Bemba; P?rigaud, Christian; Math?, Christophe

    2017-01-01

    The racemic synthesis of new carbocyclic nucleoside methylphosphonate analogues bearing purine bases (adenine and guanine) was accomplished using bio-sourced furfuryl alcohol derivatives. All compounds were prepared using a Mitsunobu coupling between the heterocyclic base and an appropriate carbocyclic precursor. After deprotection, the compounds were evaluated for their activity against a large number of viruses. However, none of them showed significant antiviral activity or cytotoxicity.

  5. Model synthesis of six-membered carbocyclic spironucleosides

    Czech Academy of Sciences Publication Activity Database

    Nencka, Radim; Hřebabecký, Hubert; Dračínský, Martin

    2010-01-01

    Roč. 75, č. 12 (2010), s. 1259-1272 ISSN 0010-0765 R&D Projects: GA MŠk 1M0508 Institutional research plan: CEZ:AV0Z40550506 Keywords : spironucleosides * carbocyclic * Bucherer-Bergs reaction * Michaels addition * tandem reaction Subject RIV: CC - Organic Chemistry Impact factor: 0.853, year: 2010

  6. Synthesis of carbocyclic homo-N-nucleosides from iridoids

    DEFF Research Database (Denmark)

    Franzyk, Henrik; Rasmussen, Jon Holbech; Mazzei, Rafaele Antonio

    1998-01-01

    Two iridoid glucosides, antirrhinoside (1) and catalpol (2), were converted into selectively protected polysubstituted cyclopentylmethanols, which were subsequently used to prepare carbocyclic homo-N-nucleosides (5, 6 and 14). A purine moiety was introduced either by the Mitsunobu reaction...... or by substitution of a primary triflate with the tetrabutylammonium salt of 6-iodopurine. The latter method was superior with regard to both ease of purification and yield. The N-9 vs. N-7 regioselectivity of the salts of different 6-substituted purine derivatives was briefly investigated....

  7. Stereoselective synthesis of 2'-fluoro-6'-methylene carbocyclic adenosine via Vince lactam.

    Science.gov (United States)

    Singh, Uma S; Mishra, Ram C; Shankar, Ravi; Chu, Chung K

    2014-05-02

    2'-Fluoro-6'-methylene carbocyclic adenosine (FMCA) is a potent and selective inhibitor of wild type as well as drug-resistant hepatitis B virus (HBV) mutants. FMCA demonstrated excellent anti-HBV activity against both adefovir-resistant and lamivudine-resistant double (rtL180M/rtM204V) mutants as well as in lamivudine/entecavir triple mutants (L180M+S202G+M204V) in vitro. Its monophosphate prodrug (FMCAP) demonstrated a greater than 12-fold increase of anti-HBV activity in comparison to that of the nucleoside without elevation of cellular toxicity. In the preliminary in vivo study in chimeric mice harboring the lamivudine/entecavir triple mutant, FMCAP effectively reduced HBV viral load, while entecavir was not effective. Therefore, it was of great interest to develop an efficient synthetic procedure to support the preclinical investigation. In this article, a new approach for the synthesis of FMCA from a readily available starting material (Vince lactam) in 16 steps is described. An efficient and practical methodology for stereospecific preparation of a versatile carbocyclic key intermediate, D-2'-fluoro-6'-methylene cyclopentanol 14, has been developed from diazotization, elimination, stereoselective epoxidation, fluorination, and oxidation-reduction sequence of the Vince lactam in 14 steps. The utility of D-2'-fluoro-6'-methylene cyclopentanol 14 is demonstrated in the preparation of FMCA using the Mitsunobu coupling to introduce the adenine base to synthesize the final nucleoside.

  8. Synthesis of novel racemic carbocyclic nucleosides derived from 5,6-disubstituted norbornene

    Czech Academy of Sciences Publication Activity Database

    Šála, Michal; Hřebabecký, Hubert; Dračínský, Martin; Masojídková, Milena; De Palma, A. M.; Neyts, J.; Holý, Antonín

    2010-01-01

    Roč. 75, č. 1 (2010), s. 1-20 ISSN 0010-0765 R&D Projects: GA MŠk 1M0508; GA AV ČR 1QS400550501 Institutional research plan: CEZ:AV0Z40550506 Keywords : carbocyclic nucleosides * norbornenes * Coxsackie virus Subject RIV: CC - Organic Chemistry Impact factor: 0.853, year: 2010

  9. Total syntheses of hyperforin and papuaforins A-C, and formal synthesis of nemorosone through a gold(I)-catalyzed carbocyclization.

    Science.gov (United States)

    Bellavance, Gabriel; Barriault, Louis

    2014-06-23

    The remarkable biological activities of polyprenylated polycyclic acylphloroglucinols (PPAPs) combined with their highly decorated bicyclo[3.3.1]nonane-2,4,9-trione frameworks have inspired synthetic organic chemists over the last decade. The concise total syntheses of four natural products PPAPs; hyperforin and papuaforins A-C, and the formal synthesis of nemorosone are reported. Key to the realization of this strategy is the short and scalable synthesis of densely substituted PPAP scaffolds through a gold(I)-catalyzed 6-endo-dig carbocyclization of cyclic enol ethers for late-stage functionalization. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. Asymmetric synthesis of densely functionalized medium-ring carbocycles and lactones through modular assembly and ring-closing metathesis of sulfoximine-substituted trienes and dienynes.

    Science.gov (United States)

    Lejkowski, Michal; Banerjee, Prabal; Schüller, Sabine; Münch, Alexander; Runsink, Jan; Vermeeren, Cornelia; Gais, Hans-Joachim

    2012-03-19

    An asymmetric synthesis of densely functionalized 7-11-membered carbocycles and 9-11-membered lactones has been developed. Its key steps are a modular assembly of sulfoximine-substituted C- and O-tethered trienes and C-tethered dienynes and their Ru-catalyzed ring-closing diene and enyne metathesis (RCDEM and RCEYM). The synthesis of the C-tethered trienes and dienynes includes the following steps: 1) hydroxyalkylation of enantiomerically pure titanated allylic sulfoximines with unsaturated aldehydes, 2) α-lithiation of alkenylsulfoximines, 3) alkylation, hydroxy-alkylation, formylation, and acylation of α-lithioalkenylsulfoximines, and 4) addition of Grignard reagents to α-formyl(acyl)alkenylsulfoximines. The sulfoximine group provided for high asymmetric induction in steps 1) and 4). RCDEM of the sulfoximine-substituted trienes with the second-generation Ru catalyst stereoselectively afforded the corresponding functionalized 7-11-membered carbocyles. RCDEM of diastereomeric silyloxy-substituted 1,6,12-trienes revealed an interesting difference in reactivity. While the (R)-diastereomer gave the 11-membered carbocyle, the (S)-diastereomer delivered in a cascade of cross metathesis and RCDEM 22-membered macrocycles. RCDEM of cyclic trienes furnished bicyclic carbocycles with a bicyclo[7.4.0]tridecane and bicyclo[9.4.0]pentadecane skeleton. Selective transformations of the sulfoximine- and bissilyloxy-substituted carbocycles were performed including deprotection, cross-coupling reaction and reduction of the sulfoximine moiety. Esterification of a sulfoximine-substituted homoallylic alcohol with unsaturated carboxylic acids gave the O-tethered trienes, RCDEM of which yielded the sulfoximine-substituted 9-11-membered lactones. RCEYM of a sulfoximine-substituted 1,7-dien-10-yne showed an unprecedented dichotomy in ring formation depending on the Ru catalyst. While the second-generation Ru catalyst gave the 9-membered exo 1,3-dienyl carbocycle, the first-generation Ru

  11. Synthesis of Carbocyclic Hydantocidins via Regioselective and Diastereoselective Phosphine-Catalyzed [3 + 2]-Cycloadditions to 5-Methylenehydantoins

    Energy Technology Data Exchange (ETDEWEB)

    Pham, Tien Q.; Pyne, Stephen G.; Skelton, Brian W.; White, Allan H. (UWA); (Wollongong)

    2010-07-20

    The phosphine-catalyzed [3 + 2]-cycloaddition of 5-methylenehydantoins 4 with the ylides 5, derived from addition of tributylphosphine to the 2-butynoic acid derivatives, 6a-d, gives spiro-heterocyclic products. The camphor sultam derivative 6b gives optically active products. Noteable was that the ylides derived from ethyl 2-butynoate and the 3-(2-butynoyl)-1,3-oxazolidin-2-one derivatives 6c and 6d gave spiro-heterocyclic products with reverse regioselectivities. The N,N-dibenzylprotected cycloadduct has been converted to carbocyclic hydantocidin and 6,7-diepi-carbocyclic hydantocidin.

  12. Synthesis of novel carbocyclic nucleoside analogues derived from 7-oxabicyclo[2.2.1]heptane-2-methanol

    Czech Academy of Sciences Publication Activity Database

    Hřebabecký, Hubert; Dračínský, Martin; De Palma, A.; Neyts, J.; Holý, Antonín

    2009-01-01

    Roč. 74, č. 3 (2009), s. 487-502 ISSN 0010-0765 R&D Projects: GA MŠk 1M0508; GA AV ČR 1QS400550501 Institutional research plan: CEZ:AV0Z40550506 Keywords : carbocyclic nucleosides * purines * thymine Subject RIV: CC - Organic Chemistry Impact factor: 0.856, year: 2009

  13. Synthesis of novel carbocyclic nucleoside analogues containing bicyclo[2.2.1]hept-2-ene-2-methanol

    Czech Academy of Sciences Publication Activity Database

    Hřebabecký, Hubert; Dračínský, Martin; Holý, Antonín

    2008-01-01

    Roč. 73, č. 1 (2008), s. 44-58 ISSN 0010-0765 R&D Projects: GA MŠk 1M0508; GA AV ČR 1QS400550501; GA ČR GA203/05/0132 Institutional research plan: CEZ:AV0Z40550506 Keywords : carbocyclic nucleosides * purines * norbornenes Subject RIV: CC - Organic Chemistry Impact factor: 0.784, year: 2008

  14. Grafted Cross-Linked Polyolefin Substrates for Peptide Synthesis and Assays

    DEFF Research Database (Denmark)

    1999-01-01

    suited for use in solid-phase biosystems, notably bioassays, such as immunoassays, DNA hybridization assays or PCR amplification. The grafted chains may bear substituents which are such that the polymer-grafted cross-linked polyolefin substrate is swellable by water or aqueous media, in other words...

  15. Rhodium-catalyzed [5 + 2 + 1] cycloaddition of ene-vinylcyclopropanes and CO: reaction design, development, application in natural product synthesis, and inspiration for developing new reactions for synthesis of eight-membered carbocycles.

    Science.gov (United States)

    Wang, Yi; Yu, Zhi-Xiang

    2015-08-18

    Practical syntheses of natural products and their analogues with eight-membered carbocyclic skeletons are important for medicinal and biological investigations. However, methods and strategies to construct the eight-membered carbocycles are limited. Therefore, developing new methods to synthesize the eight-membered carbocycles is highly desired. In this Account, we describe our development of three rhodium-catalyzed cycloadditions for the construction of the eight-membered carbocycles, which have great potential in addressing the challenges in the synthesis of medium-sized ring systems. The first reaction described in this Account is our computationally designed rhodium-catalyzed two-component [5 + 2 + 1] cycloaddition of ene-vinylcyclopropanes (ene-VCPs) and CO for the diastereoselective construction of bi- and tricyclic cyclooctenones. The design of this reaction is based on the hypothesis that the C(sp(3))-C(sp(3)) reductive elimination of the eight-membered rhodacycle intermediate generated from the rhodium-catalyzed cyclopropane cleavage and alkene insertion, giving Wender's [5 + 2] cycloadduct, is not easy. Under CO atmosphere, CO insertion may occur rapidly, converting the eight-membered rhodacycle into a nine-membered rhodacycle, which then undergoes an easy C(sp(2))-C(sp(3)) reductive elimination process and furnishes the [5 + 2 + 1] product. This hypothesis was supported by our preliminary DFT studies and also served as inspiration for the development of two [7 + 1] cycloadditions: the [7 + 1] cycloaddition of buta-1,3-dienylcyclopropanes (BDCPs) and CO for the construction of cyclooctadienones, and the benzo/[7 + 1] cycloaddition of cyclopropyl-benzocyclobutenes (CP-BCBs) and CO to synthesize the benzocyclooctenones. The efficiency of these rhodium-catalyzed cycloadditions can be revealed by the application in natural product synthesis. Two eight-membered ring-containing natural products, (±)-asterisca-3(15),6-diene and (+)-asteriscanolide, have been

  16. Metallocene Based Polyolefin Nanocomposites

    Directory of Open Access Journals (Sweden)

    Walter Kaminsky

    2014-03-01

    Full Text Available One of the most efficient and versatile ways to synthesize polyolefin nanocomposites is the in-situ polymerization of olefins in the presence of nano particles by metallocene catalysts. Metallocene/methylaluminoxane (MAO catalysts are soluble in hydrocarbons and therefore they can be absorbed perfectly in solution onto the surface of particles or fibers and after addition of ethene or propene they can then catalyze a polyolefin film on the surface. Metallocene/MAO and other single site catalysts allow the synthesis of polymers with a precisely defined microstructure, tacticity, and stereoregularity as well as new copolymers with superior properties such as film clarity, high tensile strength and lower content of extractables. The polymer properties can be enlarged by the incorporation of nanofillers. The resulting polyethylene or polypropylene nanocomposites give a tremendous boost to the physical and chemical properties such as dramatically improved stiffness, high gas barrier properties, significant flame retardancy, and high crystallization rates.

  17. Design and Synthesis of Polyimides Based on Carbocyclic Pseudo-Tröger’s Base-Derived Dianhydrides for Membrane Gas Separation Applications

    KAUST Repository

    Ma, Xiaohua

    2017-07-24

    Two novel carbocyclic pseudo-Tröger’s base-derived dianhydrides, 5,6,11,12-tetrahydro-5,11-methanodibenzo[a,e][8]annulene-2,3,8,9-tetracarboxylic anhydride (CTB1) and its dione-substituted analogue 6,12-dioxo-5,6,11,12-tetrahydro-5,11-methanodibenzo[a,e][8]annulene-2,3,8,9-tetracarboxylic dianhydride (CTB2), were made and used for the synthesis of soluble polyimides of intrinsic microporosity with 3,3′-dimethylnaphthidine (DMN). The polyimides CTB1-DMN and CTB2-DMN exhibited excellent thermal stability of ∼500 °C and high BET surface areas of 580 and 469 m2 g–1, respectively. A freshly made dione-substituted CTB2-DMN membrane demonstrated promising gas separation performance with O2 permeability of 206 barrer and O2/N2 selectivity of 5.2. A higher O2 permeability of 320 barrer and lower O2/N2 selectivity of 4.2 were observed for a fresh CTB1-DMN film due to its higher surface area and less tightly packed structure as indicated by weaker charge-transfer complex interactions. Physical aging over 60 days resulted in reduction in gas permeability and moderately enhanced selectivity. CTB2-DMN exhibited notable performance with gas permeation data located between the 2008 and 2015 permeability/selectivity upper bounds for O2/N2 and H2/CH4.

  18. Novel Applications of Donor-Acceptor Cyclopropanes and Dearomatization towards the Expedient Synthesis of Highly Substituted Carbocycles

    Science.gov (United States)

    Mackay, William Daniel

    I. Lewis Acid Catalyzed (3+2)-Annulations of Donor-Acceptor Cyclopropanes and Ynamides. The Sc(OTf)3-catalyzed (3+2)-annulation of donor-acceptor cyclopropanes and ynamides is described, providing the corresponding cyclopentene sulfonamides in good to excellent yield. Deprotection and hydrolysis of the resulting cyclopentenesulfonamides delivers 2,3-substituted cyclopentanones with high diastereoselectivity. II. Kinetic Separation and Asymmetric Reactions of Norcaradiene Cycloadducts: Facilitated Access via H2O-Accelerated Cycloaddition. We exploit the Buchner reaction to access 1,2-disubstituted cyclohexadiene synthons (norcaradienes), which participate in H2O-accelerated cycloaddition with dienophiles to provide cyclopropyl-fused [2.2.2]-bicyclooctene derivatives in good yields. Regioisomeric mixtures can be kinetically separated exploiting different reaction rates in Diels-Alder reactions. meso -Diels-Alder products may be enantioselectively desymmetrized, providing highly substituted cyclohexanes with up to seven contiguous stereocenters. III. The Development of Regioisomerically Enriched Buchner Products for Use as Cyclohexadienyl Synthetic Intermediates. We have investigated two conceptual methods to generate highly regioisomerically enriched norcaradienyl intermediates through arene cyclopropanation. Intermolecular Buchner reaction of aryl diazoacetates under either thermolysis or silver(I) catalysis provide expedient routes to single regioisomeric norcaradienes, in some cases favoring the least sterically encumbered site of cyclopropanation. Intramolecular Buchner reaction of benzyl cyanodiazoacetates allow for the site-selective cyclopropanation of the tethered arene, and the installation of an activated cyclopropane for downstream functionalization. Both methods generate norcaradienes that are amenable to further transformations to generate highly stereochemically complex carbocyclic products.

  19. Synthesis of Highly Branched Polyolefins Using Phenyl Substituted α-Diimine Ni(II Catalysts

    Directory of Open Access Journals (Sweden)

    Fuzhou Wang

    2016-04-01

    Full Text Available A series of α-diimine Ni(II complexes containing bulky phenyl groups, [ArN = C(NaphthC = NAr]NiBr2 (Naphth: 1,8-naphthdiyl, Ar = 2,6-Me2-4-PhC6H2 (C1; Ar = 2,4-Me2-6-PhC6H2 (C2; Ar = 2-Me-4,6-Ph2C6H2 (C3; Ar = 4-Me-2,6-Ph2C6H2 (C4; Ar = 4-Me-2-PhC6H3 (C5; Ar = 2,4,6-Ph3C6H2 (C6, were synthesized and characterized. Upon activation with either diethylaluminum chloride (Et2AlCl or modified methylaluminoxane (MMAO, all Ni(II complexes showed high activities in ethylene polymerization and produced highly branched amorphous polyethylene (up to 145 branches/1000 carbons. Interestingly, the sec-butyl branches were observed in polyethylene depending on polymerization temperature. Polymerization of 1-alkene (1-hexene, 1-octene, 1-decene and 1-hexadecene with C1-MMAO at room temperature resulted in branched polyolefins with narrow Mw/Mn values (ca. 1.2, which suggested a living polymerization. The polymerization results indicated the possibility of precise microstructure control, depending on the polymerization temperature and types of monomers.

  20. Synthesis of novel carbocyclic nucleosides and Pro-Tides derived from 4-oxatricyclo[4.2.1.03,7]nonane-9-methanol

    Czech Academy of Sciences Publication Activity Database

    Hřebabecký, Hubert; Dračínský, Martin; Holý, Antonín

    2007-01-01

    Roč. 72, č. 10 (2007), s. 1331-1349 ISSN 0010-0765 R&D Projects: GA MŠk 1M0508; GA AV ČR 1QS400550501 Institutional research plan: CEZ:AV0Z40550506 Keywords : carbocyclic nucleosides * purines * thymine Subject RIV: CC - Organic Chemistry Impact factor: 0.879, year: 2007

  1. Synthesis of novel conformationally locked carbocyclic nucleosides derived from 3-(hydroxymethyl)bicyclo[2.2.1]heptane-2,5-diol

    Czech Academy of Sciences Publication Activity Database

    Hřebabecký, Hubert; Masojídková, Milena; Dračínský, Martin; Holý, Antonín

    2006-01-01

    Roč. 71, č. 6 (2006), s. 871-888 ISSN 0010-0765 R&D Projects: GA MŠk(CZ) 1M0508; GA ČR(CZ) GA203/05/0132 Institutional research plan: CEZ:AV0Z40550506 Keywords : azides * amines * cyclic sulfates * carbocyclic nucleosides Subject RIV: CC - Organic Chemistry Impact factor: 0.881, year: 2006

  2. Construction of Eight-Membered Carbocycles with Trisubstituted Double Bonds Using the Ring Closing Metathesis Reaction

    Directory of Open Access Journals (Sweden)

    Motoo Tori

    2010-06-01

    Full Text Available Medium sized carbocycles are particularly difficult to synthesize. Ring closing metathesis reactions (RCM have recently been applied to construct eight-membered carbocycles, but trisubstituted double bonds in the eight-membered rings are more difficult to produce using RCM reactions. In this review, model examples and our own results are cited and the importance of the preparation of suitably designed precursors is discussed. Examples of RCM reactions used in the total synthesis of natural products are also outlined.

  3. Synthesis and characterization of a microporous 6FDA-polyimide made from a novel carbocyclic pseudo Tröger's base diamine: Effect of bicyclic bridge on gas transport properties

    KAUST Repository

    Abdulhamid, Mahmoud A.

    2017-10-12

    A newly designed carbocyclic pseudo Tröger\\'s base diamine (CTB) monomer, 2,8-dimethyl-3,9-diamino-5,6,11,12-tetrahydro-5,11-methanodibenzo[a,e][8]annulene (CTBDA) and its isomeric analogue 2,8-dimethyl-(1,7)(4,10)(3,9)-diamino-5,6,11,12-tetrahydro-5,11-methanodibenzo[a,e][8]annulene (iCTBDA), were designed for the synthesis of microporous 6FDA-based polyimides (6FDA-CTBDA and 6FDA-iCTBDA). Both polyimides were soluble, exhibited excellent thermal stability of ∼490 °C, and had high surface areas of 587 m2 g−1 (6FDA-CTBDA) and 562 m2 g−1 (6FDA-iCTBDA). A 6FDA-based polyimide derived from 4,10-dimethyl-3,9-diamino-6H,12H-5,11-methanodibenzo[b,f][1,5]-diazocine (6FDA-TBDA) was made for comparison to investigate the effects of the basic tertiary nitrogen functionality in the Tröger\\'s base diamine on the polymer properties relative to the carbocyclic 6FDA-CTBDA analogue. 6FDA-TBDA displayed lower gas permeabilities but moderately higher gas-pair permselectivities than 6FDA-CTBDA. The enhanced permselectivity of 6FDA-TBDA resulted exclusively from higher diffusion-based selectivity. Direct gas sorption measurements demonstrated that the basicity in the Tröger\\'s base bridge moiety enhanced the sorption capacity of CO2 only slightly and had no effect on the CO2/CH4 solubility selectivity in 6FDA-TBDA vs. 6FDA-CTBDA.

  4. Metallocene Based Polyolefin Nanocomposites

    OpenAIRE

    Walter Kaminsky

    2014-01-01

    One of the most efficient and versatile ways to synthesize polyolefin nanocomposites is the in-situ polymerization of olefins in the presence of nano particles by metallocene catalysts. Metallocene/methylaluminoxane (MAO) catalysts are soluble in hydrocarbons and therefore they can be absorbed perfectly in solution onto the surface of particles or fibers and after addition of ethene or propene they can then catalyze a polyolefin film on the surface. Metallocene/MAO and other single site catal...

  5. Synthetic Strategies for Converting Carbohydrates into Carbocycles by the Use of Olefin Metathesis

    DEFF Research Database (Denmark)

    Madsen, Robert

    2007-01-01

    This microreview covers recent advances in the use of ring-closing metathesis for the synthesis of carbocycles from carbohydrates. Various strategies for the synthesis of a,w-dienes from carbohydrates are presented, which give rise to a large variety of dienes with different stereochemistry, prot...

  6. Functional polyolefins prepared by group 4 diamide complexes through tandem ring-opening metathesis/vinyl insertion polymerization

    OpenAIRE

    Xu, Guangjuan

    2014-01-01

    Since the intense exploration and commercialization of new polymerization technologies based on single-site and metallocene catalysts, polyolefins with new and innovative properties are produced on a multibillion pound scale per year. Although the saturated structure of polyolefins offers many merits, the non-polar nature of polyolefins limits their applications. Unsaturated copolymers hold great potential in materials chemistry, as they allow for the synthesis of functional polyolefins witho...

  7. Functionalized linear and cyclic polyolefins

    Science.gov (United States)

    Tuba, Robert; Grubbs, Robert H.

    2018-02-13

    This invention relates to methods and compositions for preparing linear and cyclic polyolefins. More particularly, the invention relates to methods and compositions for preparing functionalized linear and cyclic polyolefins via olefin metathesis reactions. Polymer products produced via the olefin metathesis reactions of the invention may be utilized for a wide range of materials applications. The invention has utility in the fields of polymer and materials chemistry and manufacture.

  8. Structure-property relationships in model polyolefins

    Science.gov (United States)

    Weimann, Peter Andrew

    Correlations between structure and properties were examined in a variety of model polyolefin blend and block copolymer systems. Anionic polymerization and catalytic hydrogenation were used to prepare the polymers, followed by characterization of structure and the properties of interest. Production of poly(vinylcyclohexane) (PVCH) through hydrogenation of poly(styrene), using a novel Pt/SiOsb2 catalyst, was examined in some detail. Kinetics were established through time sampling of reactions performed under a variety of conditions, followed by characterization of the extent of saturation. The Pt/SiOsb2 catalyst was quantitatively demonstrated to be more efficient than other heterogeneous hydrogenation catalysts for saturation of poly(styrene). Relationships between chain structure and miscibility were explored in blends of isotactic poly(propylene) (i-PP) with a series of model saturated polyolefins. An experimental correlation between conformational symmetry and miscibility in polyolefin blends guided synthesis of several model poly(ethylene/ethylethylene) random copolymers. Using small-angle neutron scattering, melt miscibility was demonstrated for "conformationally symmetric" blends of poly(ethylene/ethylethylene) random copolymers and i-PP, while "conformationally asymmetric" random copolymers phase separated from i-PP. Phase separated poly(ethylene) (PE) - PVCH block copolymers were employed in a study of crystallization of tethered PE chains in confined environments. In these materials, the glassy PVCH forced the PE to crystallize in geometries with well-defined spacing and connectivity. Effects of chain tethering were studied through comparison of "EV" diblocks to "VEV" triblocks. Increasing confinement, reflected by decreasing the domain spacing of the block copolymer, led to a reduction in crystallite size. The geometry and connectivity of the PE component also had a major influence on crystallization. Crystal growth was retarded in block copolymers where

  9. Polyolefins to thrive by 1995

    International Nuclear Information System (INIS)

    Morris, G.D.L.

    1993-01-01

    Five factors will shorten the [current] period of distress for global polyolefins producers, says George T. Scott, v.p. and general manager of olefins and derivatives for Chevron Chemical (Houston): lower feedstock costs, the weaker dollar, higher operating rates, higher converter capacity, and technical improvements at the high end of the market. The next two years will be tough, says Scott, but I am hopeful of a full recovery to reinvestment economics by 1995. Scott made his remarks in the keynote address last week at a technical conference in Houston sponsored by the Society of Plastics Engineers (Brookfield, IL). Of the five factors, lower feedstock costs are the most immediate, with ethylene, and especially propylene, mired in neart-term record lows. However, other market watchers point out that the upstream situation must now include cracker feedslates because more merchant polyolefin producers are integrated back to the monomer. With as little as one-quarter of polymer capacity supplied from the merchant olefin market, by some estimates, a dollars/1,000-cubic-feet number is now more important than a cents/pound number. Technical advances at the top of the market are another intriguing factor. In recent years, says Scott, improvements in catalysts and processes have improved operating efficiencies and costs for high-volume trains. The cutting edge work today, however, is for speciality grades and custom-designed molecules for specific applications. Such advances have the double benefit of bringing high margin materials into the market while not adding many new pounds to an oversupplied business

  10. Two convergent approaches toward novel carbocyclic C-nucleosides

    Czech Academy of Sciences Publication Activity Database

    Nencka, Radim; Šála, Michal; Dejmek, Milan; Dračínský, Martin; Holý, Antonín; Hřebabecký, Hubert

    -, č. 23 (2010), s. 4119-4130 ISSN 0039-7881 R&D Projects: GA MŠk 1M0508 Institutional research plan: CEZ:AV0Z40550506 Keywords : carbocyclic C-nucleosides * convergent approach * uracil * pyrimidines Subject RIV: CC - Organic Chemistry Impact factor: 2.260, year: 2010

  11. Synthesis of novel racemic carbocyclic nucleoside analogues derived from 4,8-dioxatricyclo[4.2.1.0 3,7]nonane-9-methanol and 4-oxatricyclo[4.3.1.0 3,7]decane-10-methanol, compounds with activity against Coxsackie viruses

    Czech Academy of Sciences Publication Activity Database

    Hřebabecký, Hubert; Dračínský, Martin; De Palma, A.; Neyts, J.; Holý, Antonín

    2009-01-01

    Roč. 74, č. 3 (2009), s. 469-485 ISSN 0010-0765 R&D Projects: GA MŠk 1M0508; GA AV ČR 1QS400550501 Institutional research plan: CEZ:AV0Z40550506 Keywords : amines * carbocyclic nucleosides * purines Subject RIV: CC - Organic Chemistry Impact factor: 0.856, year: 2009

  12. Stability of Fentanyl Citrate in Polyolefin Bags.

    Science.gov (United States)

    Donnelly, Ronald F

    2016-01-01

    Fentanyl is used to manage pain because it is a potent lipophilic opiate agonist. The stability of fentanyl in polyolefin bags when diluted to either 10 µg/mL or 50 µg/mL with sodium chloride 0.9% has not been studied. The chemical stability of fentanyl 50 µg/mL packaged in polyvinyl chloride bags has been studied, however, the stability in polyolefin bags is lacking. Polyolefin bags were aseptically filled with either 10-µg/mL or 50-µg/mL fentanyl solution. Containers were then stored at either 5°C and protected from light or 22°C and exposed to light for 93 days. Fentanyl peaks were monitored using a stability-indicatin high-performance liquid chromatographic method. Changes to color, clarity, and pH were also monitored. There were no signs of chemical degradation of fentanyl packaged in polyolefin bags at either 5°C or 22°C after storage for 93 days. Over the course of the study, all solutions remained colorless and clear. The pH showed a slight decrease during the 93 days of storage. The stability of both undiluted (50-µg/mL) and diluted (10-µg/mL) fentanyl solutions when packaged in polyolefin bags was 93 days when stored at either 5°C or 22°C. Copyright© by International Journal of Pharmaceutical Compounding, Inc.

  13. Stochastic modelling of migration from polyolefins

    NARCIS (Netherlands)

    Helmroth, I.E.; Varekamp, C.; Dekker, M.

    2005-01-01

    A method is presented to predict diffusion coefficients in polyolefins using stochastic modelling. A large number of experimental diffusion coefficients, published in the literature as one dataset, was used to derive probability distributions of diffusion coefficients in the polymers low-density

  14. Crack behavior in a welded polyolefin pipe

    Czech Academy of Sciences Publication Activity Database

    Ševčík, Martin; Hutař, Pavel; Náhlík, Luboš

    2011-01-01

    Roč. 47, č. 3 (2011), s. 263-270 ISSN 0191-5665 R&D Projects: GA ČR GD106/09/H035; GA ČR GC101/09/J027 Institutional research plan: CEZ:AV0Z20410507 Keywords : fracture mechanics * polyolefin pipe * polymer weld * stress intensity factor * graded structure Subject RIV: JL - Materials Fatigue, Friction Mechanics Impact factor: 0.409, year: 2011

  15. Magnetic Density Separation of Polyolefin Wastes

    OpenAIRE

    Hu, B.

    2014-01-01

    Polymer recycling has significantly positive impacts on the environment, economics and society. Using recycled polymer to replace virgins reduces the growing amount of post-consumer polymer wastes, decreases the demand for fossil fuel and creates local jobs. As the most used polymer types, polyolefins certainly have attracted attention of recycling. Mechanical sorting has been pointed out as the preferred route for the recovery of relatively clean and homogeneous plastic waste streams. Wherea...

  16. Extreme ultraviolet (EUV) degradation of poly(olefin sulfone)s: Towards applications as EUV photoresists

    International Nuclear Information System (INIS)

    Lawrie, Kirsten; Blakey, Idriss; Blinco, James; Gronheid, Roel; Jack, Kevin; Pollentier, Ivan; Leeson, Michael J.; Younkin, Todd R.; Whittaker, Andrew K.

    2011-01-01

    Poly(olefin sulfone)s, formed by the reaction of sulfur dioxide (SO 2 ) and an olefin, are known to be highly susceptible to degradation by radiation and thus have been identified as candidate materials for chain scission-based extreme ultraviolet lithography (EUVL) resist materials. In order to investigate this further, the synthesis and characterisation of two poly(olefin sulfone)s namely poly(1-pentene sulfone) (PPS) and poly(2-methyl-1-pentene sulfone) (PMPS), was achieved and the two materials were evaluated for possible chain scission EUVL resist applications. It was found that both materials possess high sensitivities to EUV photons; however; the rates of outgassing were extremely high. The only observed degradation products were found to be SO 2 and the respective olefin suggesting that depolymerisation takes place under irradiation in a vacuum environment. In addition to depolymerisation, a concurrent conversion of SO 2 moieties to a sulfide phase was observed using XPS.

  17. Upgrading mixed polyolefin waste with magnetic density separation.

    Science.gov (United States)

    Bakker, E J; Rem, P C; Fraunholcz, N

    2009-05-01

    Polyolefin fractions are often end fractions resulting from the recycling of end-of-life consumer products. Polypropylene (PP) and polyethylene (PE) are present in such fractions as a mixture. For instance, the ratio of PP and PE in car scrap is 70:30 on average. However, the grade of the PP and PE should typically be better than 97% to be reused again as a high quality product. Density separation of the different polyolefins can be a solution. A promising separation technique is the inverse magnetic density separator (IMDS). This paper discusses the potential of shredder residue, one of the possible polyolefin's waste stream sources for the IMDS, in detail. Experiments with the separation of polyolefins with an IMDS prototype show both high grade and high recovery. The paper concludes with the economic opportunities of the IMDS in the recycling of polyolefins.

  18. Diastereoselective Flexible Synthesis of Carbocyclic C-Nucleosides

    Czech Academy of Sciences Publication Activity Database

    Maier, L.; Khirsariya, P.; Hylse, O.; Adla, S.K.; Cernova, L.; Poljak, M.; Krajčovičová, S.; Weis, E.; Drápela, Stanislav; Souček, Karel; Paruch, K.

    2017-01-01

    Roč. 82, č. 7 (2017), s. 3382-3402 ISSN 0022-3263 Institutional support: RVO:68081707 Keywords : mitsunobu * catalysis * alcohols Subject RIV: CC - Organic Chemistry OBOR OECD: Organic chemistry Impact factor: 4.849, year: 2016

  19. Stability of tacrolimus solutions in polyolefin containers.

    Science.gov (United States)

    Lee, Jun H; Goldspiel, Barry R; Ryu, Sujung; Potti, Gopal K

    2016-02-01

    Results of a study to determine the stability of tacrolimus solutions stored in polyolefin containers under various temperature conditions are reported. Triplicate solutions of tacrolimus (0.001, 0.01, and 0.1 mg/mL) in 0.9% sodium chloride injection or 5% dextrose injection were prepared in polyolefin containers. Some samples were stored at room temperature (20-25 °C); others were refrigerated (2-8 °C) for 20 hours and then stored at room temperature for up to 28 hours. The solutions were analyzed by stability-indicating high-performance liquid chromatography (HPLC) assay at specified time points over 48 hours. Solution pH was measured and containers were visually inspected at each time point. Stability was defined as retention of at least 90% of the initial tacrolimus concentration. All tested solutions retained over 90% of the initial tacrolimus concentration at all time points, with the exception of the 0.001-mg/mL solution prepared in 0.9% sodium chloride injection, which was deemed unstable beyond 24 hours. At all evaluated concentrations, mean solution pH values did not change significantly over 48 hours; no particle formation was detected. During storage in polyolefin bags at room temperature, a 0.001-mg/mL solution of tacrolimus was stable for 24 hours when prepared in 0.9% sodium chloride injection and for at least 48 hours when prepared in 5% dextrose injection. Solutions of 0.01 and 0.1 mg/mL prepared in either diluent were stable for at least 48 hours, and the 0.01-mg/mL tacrolimus solution was also found to be stable throughout a sequential temperature protocol. Copyright © 2016 by the American Society of Health-System Pharmacists, Inc. All rights reserved.

  20. Applications of polyolefins in the nuclear industry

    International Nuclear Information System (INIS)

    Erambert, M.; Goavec, P.

    1984-01-01

    The environment of a nuclear power plant often imposes impossible conditions on wires and cables. Cable manufacturers make great use of polymers, and the properties of the latter are limited in all the fields imposed: radiation, ageing, fire, corrosion. ACOME presents a cross-linked fireproof polyolefin, the properties of which have been verified in long-term tests: with very different ageing temperatures and times, very variable dose rates and very long simultaneous cycles. After all the tests proposed, the mechanical characteristics still made winding on cores possible. The electrical characteristics were very good, and fireproofing was unaffected [fr

  1. A compendium of cyclic sugar amino acids and their carbocyclic and heterocyclic nitrogen analogues.

    Science.gov (United States)

    Risseeuw, Martijn; Overhand, Mark; Fleet, George W J; Simone, Michela I

    2013-10-01

    This compendium focuses on functionalised sugar amino acids (SAAs) and their 3- to 6-membered nitrogen heterocyclic and carbocyclic analogues. The main benefit of using SAAs and their related nitrogen and carbon congeners in the production of peptidomimetics and glycomimetics is that their properties can be readily altered via modification of their ring size, chemical manipulation of their numerous functional groups and fine-tuning of the stereochemical arrangement of their ring substituents. These building blocks provide access to hydrophilic and hydrophobic peptide isosteres whose physical properties allow entry to a region of chemotherapeutic space which is still under-explored by medicinal chemists. These building blocks are also important in providing amino acids whose inherent conformational bias leads to predisposition to secondary structure upon oligomerisation in relatively short sequences. These foldamers, particularly those containing ω-amino acids, provide an additional opportunity to expand access to the control of structures by artificial peptides. The synthesis and biological evaluation of these building blocks in glycomimetics and peptidomimetics systems keep expanding the reach of the glycosciences to the medical sciences, provide a greater outlook onto the wide range of cellular functions of saccharides and their derivatives involved and greater insight into the nature of oligosaccharide and protein folding.

  2. Degradation of polyolefine wastes into liquid fuels

    International Nuclear Information System (INIS)

    Tyminski, B.; Zwolinski, K.; Jurczyk, R.

    2006-01-01

    In Poland, the consumption of polymers like polyethylene, polypropylene and polystyrene amounts is nearly one million tons per year. Most of the products made of these polymers becomes wastes in short time. Polymers are very resistant to biodegradation, therefore technologies of their transformation into useful materials should be developed. In our Institute, the technology of catalytic cracking of polyolefines into liquid fuels is studied. Experiments are concentrated on the selection of proper catalyst and on the construction of continuously operated installation for cracking of polyolefine wastes. Experiments on the selection of catalyst were performed in a laboratory scale batch reactor. A big laboratory installation with a yield of ca. 1 kg/h of liquid products was tested with positive results and plans are to construct a pilot plant installation with a yield of 30 kg/h of liquid products. The products of catalytic cracking are separated in a distillation column into gas, gasoline, light oil and heavy oil fractions. The gas is used for heating the reactor. The heavy oil fraction is recycled to the reactor and the gasoline and light oil fractions are the final products. The gasoline fraction can be used as a component of motor gasoline and the light oil fraction can be used as a component of diesel fuel or as a heating oil. (author)

  3. Thermoplastic polyurethane (TPU)/polyolefin (PO) blends

    Science.gov (United States)

    Lu, Qiwei

    Thermoplastic polyurethane (TPU) is a very important material with high versatility and superior physical properties. Melt blending TPU with metallocene polyolefin (PO) can lower TPU cost and improve polyolefin properties like abrasion resistance, adhesion, and paintability. Since TPU and non-polar PO blends are completely immiscible, efficient compatibilizers become the key issue and remain challenging. My main thesis work is to develop and study compatibilized TPU/PO blends. Although reactive compatibilization is considered the most efficient method, fast interfacial reactions between highly reactive functional groups are necessary to generate compatibilizers within usually short processing time. It is known that the urethane linkage (carbamate -NHCOO-) in TPU can reversibly dissociate to generate highly reactive isocyanates at melt temperatures. To find out the best reactive compatibilization, three approaches were employed on different molecular scales: (1) model urethane compound (dibutyl & dioctyl 4,4'-methylenebis(phenyl carbamate)) and small functional molecule (primary amine, secondary amine, hydroxyl, acid, anhydride, and epoxide) reactions at 200°C monitored by nuclear magnetic resonance and Fourier-transform infrared to examine the basic chemistry; (2) short, model TPU's with different chemical structures blended with functional polymers including poly(ethylene glycol) and polybutadiene to explore the effect of interface in immiscible mixtures; (3) melt blending of a commercial TPU with polypropylene (PP), further involving more complicated morphology, using different types of functional PP's (note: amine functional PP's were prepared by melt amination) as compatibilizers followed by rheological, morphological, thermal, and mechanical characterizations. Besides the core thesis project on TPU blends, other related work that has been accomplished includes: (1) adhesion between TPU and PP; (2) rheological properties of TPU; (3) block copolymer formation

  4. Oxidation of nano-reinforced polyolefins

    International Nuclear Information System (INIS)

    Gutierrez Castro, G.G.

    2010-11-01

    Nano-composite materials attract search due to their improvements on barrier properties by incorporating low level of nano-filler of 5%w. Nowadays, organically modified montmorillonite (MMT-O) is the most used filler due to its high aspect ratio which permits stronger clay/polymer interactions. If nano-reinforced materials are highly performing, the ways in which clay presence affects polyolefin durability have not being subject of a rigorous study, thus they are not yet clear. Our goal was to examine unstabilized clay polypropylene and unstabilized clay polyethylene nano composites to get a better comprehension of the clay effects on their thermo-oxidation process under low temperatures. The effects induced by a dual physic-chemical nature of the clay were explored. The problem was tackled from both experimental and theoretical point of views for degradation process not controlled and controlled by oxygen diffusion (homogenous and heterogeneous respectively). It seems that MMT-O speeds up oxidation. This phenomenon was modeled by adding a catalytic reaction between metallic particles initially present in the MMT-O and hydroperoxide groups (main responsible of oxidation). Regarding the oxygen permeability two situations were confronted: for the clay polypropylene system a decrease of 45% of oxygen permeability was measured. On the other hand, no variation was found for the polyethylene case. This effect was attributed to the fact that polyethylene nano-composite reached a blend morphology less developed than those of the polypropylene nano-composite. Kinetics and oxidation products profiles across the sample thickness were simulated for both systems by coupling oxidation reactions with oxygen diffusion equations. For the polyethylene case, the effects induced by oxidation on molar mass and crystalline morphology were also simulated. Finally, based on a structure-property relationship, simulations of mechanic modulus profiles were performed for the heterogeneous

  5. Development of optical marker for polyolefin processes

    International Nuclear Information System (INIS)

    Marchini, Leonardo Guedes

    2013-01-01

    Research and publications about luminescent polymers have been developed in the last years for the academic innovation; however the industrial application has been very limited in this area. Processed Optical markers are few explored due the difficult to process luminescent polymeric materials with stable luminescence. The materials used to process luminescent polypropylene (PP) were polyamide 6 (PA6) doped with europium complex [Eu(tta) 3 (H 2 O) 2 ] obtained through the dilution and casting process. The polyolefins because they are inert, do not fit the common procedure of doping, in consequence, in this work luminescent polypropylene was indirectly prepared by polyamide 6 doped with europium complex through extrusion process. Product characterization was done using Thermal gravimetry analysis (TG), Differential Scanning Calorimetric (DSC), X-Ray Diffraction (XRD), Infrared spectroscopy (FTIR) and spectro fluorescence of emission and excitation. The blend PP/PA6:Eu(tta) 3 presented luminescent properties, after semi-industrial process, as observed in the narrow bands of intra configuration transitions- 4f 6 relatives to energy levels 7 F 0 → 5 L 6 (394nm), 7 F 0 → 5 D 3 (415nm), 7 F 0 → 5 D 2 (464nm), 7 F 0 → 5 D 1 (525nm) e 7 F 0 → 5 D 0 (578nm) of emission spectrum. Red light of the pellets or film is emitted when excited in UV lamp (365nm). TG results showed under O 2 atmosphere that PP doped with PA6:Eu(tta) 3 was more stable than pure PP. In this work was processed luminescent PP/PA6:Eu(tta) 3 with properties of thermal and photo stability which can be used as optical marker in polymer processing. (author)

  6. Enhanced antioxidant activity of polyolefin films integrated with grape tannins.

    Science.gov (United States)

    Olejar, Kenneth J; Ray, Sudip; Kilmartin, Paul A

    2016-06-01

    A natural antioxidant derived from an agro-waste of the wine industry, grape tannin, was incorporated by melt blending into three different polyolefins (high-density polyethylene, linear low-density polyethylene and polypropylene) to introduce antioxidant functionality. Significant antioxidant activity was observed at 1% tannin inclusion in all polymer blends. The antioxidant activity was observed to increase steadily with a greater concentration of grape tannins, the highest increases being seen with polypropylene. The mechanical and thermal properties of the polymer films following antioxidant incorporation were minimally altered with up to 3% grape tannins. All of the polyolefin-grape tannin films successfully passed the leachability test following USP661 standard protocol. Superior antioxidant activity was established in polyolefin thin films by utilization of a bulk grape extract obtained from winery waste. Significant increases in antioxidant activity were seen with 1% extract inclusion. This not only demonstrates the potential for food packaging applications of the polyolefin blends, but also valorizes the agro-waste. © 2015 Society of Chemical Industry. © 2015 Society of Chemical Industry.

  7. Compatibilization as a procedure for recycling of commingled polyolefin waste

    Czech Academy of Sciences Publication Activity Database

    Kruliš, Zdeněk; Kokta, B. V.; Horák, Zdeněk; Michálková, Danuše; Fortelný, Ivan

    2001-01-01

    Roč. 286, č. 3 (2001), s. 156-160 ISSN 1438-7492 R&D Projects: GA AV ČR IBS4050008; GA AV ČR KSK2050602 Institutional research plan: CEZ:AV0Z4050913 Keywords : recycling * reactive compatibilization * polyolefin waste Subject RIV: CD - Macromolecular Chemistry Impact factor: 0.835, year: 2001

  8. Can Latin America fill the U.S. polyolefin deficit?

    International Nuclear Information System (INIS)

    Sagel, E.

    2006-01-01

    Strategic issues for the North American polyolefin industry were discussed with reference to oil and gas price forecasts, oil capacity increases, and high density polyethylene production and ethylene integration costs. The overall polyolefin trade balance in North America was also explored. It was cautioned that unless a significant amount of new capacity is built in the United States, it is anticipated that by 2008, the United States will become a net importer of polyolefin resins. Currently exported product will be used increasingly in the domestic market to meet demand growth. This shift from being a net exporter of resins can be attributed to the high cost of feedstocks and the lack of investment in new capacity throughout the region. In contrast, there have been several proposals for new capacity in Latin America in the past several years. Since there is already an important level of commerce and trade between North and South America, countries with access to the Caribbean basin, are logistically well situated to serve the North American market. The availability of low cost feedstocks in countries such as Trinidad, Venezuela and Bolivia add to the attractiveness of the region for the development of new petrochemical capacity. This paper examined the status of the different proposed projects in Latin America and analyzed the potential opportunities that exist for North American producers to collaborate in those projects. The general trade balance of the continent was reviewed in order to verify if the traditional seclusion of America's polyolefin market can be maintained in the future. It was concluded that even if all projects in Latin America are launched, the Americas will still be in a net deficit position. Under the right circumstances, the Middle East will be the global supplier of commodity polyolefins that could extend to the Americas. It was emphasized that companies should be prepared for feedstock advantaged investments, alliances, acquisitions and

  9. Regio- and stereodivergent antibiotic oxidative carbocyclizations catalysed by Rieske oxygenase-like enzymes

    Science.gov (United States)

    Sydor, Paulina K.; Barry, Sarah M.; Odulate, Olanipekun M.; Barona-Gomez, Francisco; Haynes, Stuart W.; Corre, Christophe; Song, Lijiang; Challis, Gregory L.

    2011-05-01

    Oxidative cyclizations, exemplified by the biosynthetic assembly of the penicillin nucleus from a tripeptide precursor, are arguably the most synthetically powerful implementation of C-H activation reactions in nature. Here, we show that Rieske oxygenase-like enzymes mediate regio- and stereodivergent oxidative cyclizations to form 10- and 12-membered carbocyclic rings in the key steps of the biosynthesis of the antibiotics streptorubin B and metacycloprodigiosin, respectively. These reactions represent the first examples of oxidative carbocyclizations catalysed by non-haem iron-dependent oxidases and define a novel type of catalytic activity for Rieske enzymes. A better understanding of how these enzymes achieve such remarkable regio- and stereocontrol in the functionalization of unactivated hydrocarbon chains will greatly facilitate the development of selective man-made C-H activation catalysts.

  10. Acid-functionalized polyolefin materials and their use in acid-promoted chemical reactions

    Science.gov (United States)

    Oyola, Yatsandra; Tian, Chengcheng; Bauer, John Christopher; Dai, Sheng

    2016-06-07

    An acid-functionalized polyolefin material that can be used as an acid catalyst in a wide range of acid-promoted chemical reactions, wherein the acid-functionalized polyolefin material includes a polyolefin backbone on which acid groups are appended. Also described is a method for the preparation of the acid catalyst in which a precursor polyolefin is subjected to ionizing radiation (e.g., electron beam irradiation) of sufficient power and the irradiated precursor polyolefin reacted with at least one vinyl monomer having an acid group thereon. Further described is a method for conducting an acid-promoted chemical reaction, wherein an acid-reactive organic precursor is contacted in liquid form with a solid heterogeneous acid catalyst comprising a polyolefin backbone of at least 1 micron in one dimension and having carboxylic acid groups and either sulfonic acid or phosphoric acid groups appended thereto.

  11. The role of lubracants in reactive compatibilization of polyolefin blends

    Czech Academy of Sciences Publication Activity Database

    Hlavatá, Drahomíra; Kruliš, Zdeněk; Horák, Zdeněk; Lednický, František; Hromádková, Jiřina

    2001-01-01

    Roč. 176, - (2001), s. 93-106 ISSN 1022-1360. [International Conference on Polymer Modification, Degradation and Stabilization /1./. Palermo, 03.09.2000-07.09.2000] R&D Projects: GA ČR GA106/99/0556; GA AV ČR IBS4050008; GA AV ČR KSK2050602 Institutional research plan: CEZ:AV0Z4050913 Keywords : polyolefins * recycling * reactive compatibilization Subject RIV: CD - Macromolecular Chemistry Impact factor: 0.634, year: 2001

  12. Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block Copolymers

    Directory of Open Access Journals (Sweden)

    Chung Sol Kim

    2017-10-01

    Full Text Available Triblock copolymers of polystyrene (PS and a polyolefin (PO, e.g., PS-block-poly(ethylene-co-1-butene-block-PS (SEBS, are attractive materials for use as thermoplastic elastomers and are produced commercially by a two-step process that involves the costly hydrogenation of PS-block-polybutadiene-block-PS. We herein report a one-pot strategy for attaching PS chains to both ends of PO chains to construct PS-block-PO-block-PS directly from olefin and styrene monomers. Dialkylzinc compound containing styrene moieties ((CH2=CHC6H4CH2CH22Zn was prepared, from which poly(ethylene-co-propylene chains were grown via “coordinative chain transfer polymerization” using the pyridylaminohafnium catalyst to afford di-end functional PO chains functionalized with styrene and Zn moieties. Subsequently, PS chains were attached at both ends of the PO chains by introduction of styrene monomers in addition to the anionic initiator Me3SiCH2Li·(pmdeta (pmdeta = pentamethyldiethylenetriamine. We found that the fraction of the extracted PS homopolymer was low (~20% and that molecular weights were evidently increased after the styrene polymerization (ΔMn = 27–54 kDa. Transmission electron microscopy showed spherical and wormlike PS domains measuring several tens of nm segregated within the PO matrix. Optimal tensile properties were observed for the sample containing a propylene mole fraction of 0.25 and a styrene content of 33%. Finally, in the cyclic tensile test, the prepared copolymers exhibited thermoplastic elastomeric properties with no breakage up over 10 cycles, which is comparable to the behavior of commercial-grade SEBS.

  13. Nanocomposite fibers and film containing polyolefin and surface-modified carbon nanotubes

    Science.gov (United States)

    Chu,Benjamin; Hsiao, Benjamin S.

    2010-01-26

    Methods for modifying carbon nanotubes with organic compounds are disclosed. The modified carbon nanotubes have enhanced compatibility with polyolefins. Nanocomposites of the organo-modified carbon nanotubes and polyolefins can be used to produce both fibers and films having enhanced mechanical and electrical properties, especially the elongation-to-break ratio and the toughness of the fibers and/or films.

  14. Method of solution preparation of polyolefin class polymers for electrospinning processing included

    Science.gov (United States)

    Rabolt, John F. (Inventor); Lee, Keun-Hyung (Inventor); Givens, Steven R. (Inventor)

    2011-01-01

    A process to make a polyolefin fiber which has the following steps: mixing at least one polyolefin into a solution at room temperature or a slightly elevated temperature to form a polymer solution and electrospinning at room temperature said polymer solution to form a fiber.

  15. Ring-size-selective construction of fluorine-containing carbocycles via intramolecular iodoarylation of 1,1-difluoro-1-alkenes

    Directory of Open Access Journals (Sweden)

    Takeshi Fujita

    2017-12-01

    Full Text Available 1,1-Difluoro-1-alkenes bearing a biaryl-2-yl group effectively underwent site-selective intramolecular iodoarylation by the appropriate cationic iodine species. Iodoarylation of 2-(2-aryl-3,3-difluoroallylbiaryls proceeded via regioselective carbon–carbon bond formation at the carbon atoms in β-position to the fluorine substituents, thereby constructing dibenzo-fused six-membered carbocycles bearing a difluoroiodomethyl group. In contrast, 2-(3,3-difluoroallylbiaryls underwent a similar cyclization at the α-carbon atoms to afford ring-difluorinated seven-membered carbocycles.

  16. Selection criteria for recycled polyolefins from urban wastes by using TG analysis

    Directory of Open Access Journals (Sweden)

    Adhemar Ruvolo-Filho

    2007-12-01

    Full Text Available The thermal behavior of a mixture of recycled polyolefins (PE/PP mix, variously colored recycled polyolefins, recycled polyolefin blends and recycled polyolefin/PET blends was analyzed by thermogravimetry. Atmospheres of nitrogen and synthetic air were used to compare the effects of inert and oxidative medium. Four characteristic temperatures, T1, T2, T3 and T4, related to oxidative processes and atmospheric conditions, were defined. Relationships between T1, T2, T3 and T4 and comparing pigmented and transparent material allow assessing the effect of different pigments on volatilization, oxidation and onset temperatures of decomposition processes. These analyses provide preliminary parameters for selecting acceptable processing temperature conditions of recycled household and engineering plastics, and provide a few criteria to select colored recycled polyolefins.

  17. Development of highly fire-retardant irradiated polyolefin cables

    International Nuclear Information System (INIS)

    Ueno, Keiji; Inui, Toshifumi; Uda, Ikujiro

    1982-01-01

    In recent years, motors, automobiles, heaters, etc., have been made into light weight and compact form in view of labour-saving and energy-saving. For this purpose, the wires for the electrical appliances used for these equipment are required to reduce insulation thickness and to improve heat resistance. On the other hand, the requirement for fire-retardant property has become severer than before from the viewpoint of safety. As an insulation for the wires which meets such requirement, the polyolefin cross-linked by irradiation was investigated, and the heat-resistant, highly fire-retardant, polyolefin-insulated wires have been developed, which have passed vertical combustion test (VW-1) and have the insulation thickness of 0.4 mm (voltage rating 300V) and UL standard 125 deg C and 150 deg C grades. Fire-retardant polyolefin resin is normally obtained by adding halogen series flame retarders. The selection of flame retarders requires the investigation on high thermal stability, high flame retardation, no impedance to cross-linking, and good dispersion into polymers. The evaluation of heat resistance performed on two points, thermal aging and thermal deformation. The use of oxidation inhibitors is indispensable to improve the anti-thermal aging capability, but it is important to balance the requirements well by combining oxidation inhibitors, considering thermal deformation, colouring and discolouration. By comparative test with silicone rubber, cross-linked polyethylene and cross-linked PVC-insulated wires, the characteristics of highly fire-retardant wires, insulated with polyethylene cross-linked by irradiation, are described about the fireretardation, thermal deformation, thermal aging resistance, electrical characteristics and oil resistance. (Wakatsuki, Y.)

  18. Pyrolysis of polyolefins for increasing the yield of monomers’ recovery

    International Nuclear Information System (INIS)

    Donaj, Pawel J.; Kaminsky, W.; Buzeto, F.; Yang, W.

    2012-01-01

    Highlights: ► Thermal and catalytic pyrolysis of mixed polyolefins in fluidized bed has been studied. ► We tested applicability of a commercial Ziegler–Natta catalyst (Z–N: TiCl 4 /MgCl 2 ). ► The catalyst has a strong influence on product distribution, increasing gas fraction. ► At 650 °C the monomer generation increased by 55% when the catalyst was used. ► We showed the concept of treatment of mixed polyolefins without a need of separation. - Abstract: Pyrolysis of plastic waste is an alternative way of plastic recovery and could be a potential solution for the increasing stream of solid waste. The objective of this work was to increase the yield the gaseous olefins (monomers) as feedstock for polymerization process and to test the applicability of a commercial Ziegler–Natta (Z–N): TiCl 4 /MgCl 2 for cracking a mixture of polyolefins consisted of 46% wt. of low density polyethylene (LDPE), 30% wt. of high density polyethylene (HDPE) and 24% wt. of polypropylene (PP). Two sets of experiments have been carried out at 500 and 650 °C via catalytic pyrolysis (1% of Z–N catalyst) and at 650 and 730 °C via only-thermal pyrolysis. These experiments have been conducted in a lab-scale, fluidized quartz-bed reactor of a capacity of 1–3 kg/h at Hamburg University. The results revealed a strong influence of temperature and presence of catalyst on the product distribution. The ratios of gas/liquid/solid mass fractions via thermal pyrolysis were: 36.9/48.4/15.7% wt. and 42.4/44.7/13.9% wt. at 650 and 730 °C while via catalytic pyrolysis were: 6.5/89.0/4.5% wt. and 54.3/41.9/3.8% wt. at 500 and 650 °C, respectively. At 650 °C the monomer generation increased by 55% up to 23.6% wt. of total pyrolysis products distribution while the catalyst was added. Obtained yields of olefins were compared with the naphtha steam cracking process and other potentially attractive processes for feedstock generation. The concept of closed cycle material flow for

  19. Thermoplastic Adhesives based on polyolefin and olefinic copolymers

    Science.gov (United States)

    Paul, Rituparna

    2014-03-01

    H.B. Fuller has been a leading global industrial adhesive manufacturer for over 125 years. It is a company with a rich history of consistently delivering adhesive innovations for enhancing product performance in the market place. H.B. Fuller technologies/products find application in several markets including packaging, personal hygiene and nonwovens, durable assembly and electronics. In this presentation, H. B. Fuller's technology innovation journey will be shared with emphasis on groundbreaking technologies/products based on polyolefin and olefin copolymers.

  20. New carbocyclic nucleoside analogues built on a bicyclo[2.2.2]octane-2,2-dimethanol template

    Czech Academy of Sciences Publication Activity Database

    Hřebabecký, Hubert; Dračínský, Martin; Holý, Antonín

    2009-01-01

    Roč. 74, č. 9 (2009), s. 1425-1441 ISSN 0010-0765 R&D Projects: GA MŠk 1M0508; GA AV ČR 1QS400550501 Institutional research plan: CEZ:AV0Z40550506 Keywords : carbocyclic nucleosides * purines * Mitsunobu reaction Subject RIV: CC - Organic Chemistry Impact factor: 0.856, year: 2009

  1. New Palladium-Catalyzed Approaches to Heterocycles and Carbocycles

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Qinhua [Iowa State Univ., Ames, IA (United States)

    2004-12-19

    The tert-butylimines of o-(1-alkynyl)benzaldehydes and analogous pyridinecarbaldehydes have been cyclized under very mild reaction conditions in the presence of I2, ICl, PhSeCl, PhSCl and p-O2NC6H4SCl to give the corresponding halogen-, selenium- and sulfur-containing disubstituted isoquinolines and naphthyridines, respectively. Monosubstituted isoquinolines and naphthyridines have been synthesized by the metal-catalyzed ring closure of these same iminoalkynes. This methodology accommodates a variety of iminoalkynes and affords the anticipated heterocycles in moderate to excellent yields. The Pd(II)-catalyzed cyclization of 2-(1-alkynyl)arylaldimines in the presence of various alkenes provides an efficient way to synthesize a variety of 4-(1-alkenyl)-3-arylisoquinolines in moderate to excellent yields. The introduction of an ortho-methoxy group on the arylaldimine promotes the Pd-catalyzed cyclization and stabilizes the resulting Pd(II) intermediate, improving the yields of the isoquinoline products. Highly substituted naphthalenes have been synthesized by the palladium-catalyzed annulation of a variety of internal alkynes, in which two new carbon-carbon bonds are formed in a single step under relatively mild reaction conditions. This method has also been used to synthesize carbazoles, although a higher reaction temperature is necessary. The process involves arylpalladation of the alkyne, followed by intramolecular Heck olefination and double bond isomerization. This method accommodates a variety of functional groups and affords the anticipated highly substituted naphthalenes and carbazoles in good to excellent yields. Novel palladium migratiodarylation methodology for the synthesis of complex fused polycycles has been developed, in which one or more sequential Pd-catalyzed intramolecular migration processes involving C-H activation are employed. The chemistry works best with electron-rich aromatics, which is in agreement

  2. Method for the preparation of carbon fiber from polyolefin fiber precursor

    Energy Technology Data Exchange (ETDEWEB)

    Naskar, Amit Kumar; Hunt, Marcus Andrew; Saito, Tomonori

    2017-11-28

    Methods for the preparation of carbon fiber from polyolefin fiber precursor, wherein the polyolefin fiber precursor is partially sulfonated and then carbonized to produce carbon fiber. Methods for producing hollow carbon fibers, wherein the hollow core is circular- or complex-shaped, are also described. Methods for producing carbon fibers possessing a circular- or complex-shaped outer surface, which may be solid or hollow, are also described.

  3. Rheological characterization of polyolefin composites with reduced flammability

    Science.gov (United States)

    Habrova, Veronika; Kalendova, Alena; Paravanova, Gordana

    2012-07-01

    In this work, the low-flammability halogen-free polyolefin composites were characterized with three rheological methods. In the extrusion process of the studied materials the end-products with a dissimilar surface quality were produced. Therefore, the diverse melt flow behaviours evaluated with common rheological techniques were also expected. Nevertheless, the conventional rotational and capillary rheometries were not able to describe the differences between investigated flame retarded composites in optimal way. Thus, the non-conventional rheological die Shark skin, originally designed to detect flow instabilities, was tested as a third possibility in order to better understand rheology of the filled polymer melts. It was found that the Shark skin technique is able to characterize the studied two kind flame retardants composites and can also be helpful to qualify the production bathes with identical additives/polymer formulation.

  4. Pyrolysis of polyolefins for increasing the yield of monomers' recovery.

    Science.gov (United States)

    Donaj, Pawel J; Kaminsky, W; Buzeto, F; Yang, W

    2012-05-01

    Pyrolysis of plastic waste is an alternative way of plastic recovery and could be a potential solution for the increasing stream of solid waste. The objective of this work was to increase the yield the gaseous olefins (monomers) as feedstock for polymerization process and to test the applicability of a commercial Ziegler-Natta (Z-N): TiCl(4)/MgCl(2) for cracking a mixture of polyolefins consisted of 46%wt. of low density polyethylene (LDPE), 30%wt. of high density polyethylene (HDPE) and 24%wt. of polypropylene (PP). Two sets of experiments have been carried out at 500 and 650°C via catalytic pyrolysis (1% of Z-N catalyst) and at 650 and 730°C via only-thermal pyrolysis. These experiments have been conducted in a lab-scale, fluidized quartz-bed reactor of a capacity of 1-3kg/h at Hamburg University. The results revealed a strong influence of temperature and presence of catalyst on the product distribution. The ratios of gas/liquid/solid mass fractions via thermal pyrolysis were: 36.9/48.4/15.7%wt. and 42.4/44.7/13.9%wt. at 650 and 730°C while via catalytic pyrolysis were: 6.5/89.0/4.5%wt. and 54.3/41.9/3.8%wt. at 500 and 650°C, respectively. At 650°C the monomer generation increased by 55% up to 23.6%wt. of total pyrolysis products distribution while the catalyst was added. Obtained yields of olefins were compared with the naphtha steam cracking process and other potentially attractive processes for feedstock generation. The concept of closed cycle material flow for polyolefins has been discussed, showing the potential benefits of feedstock recycling in a plastic waste management. Copyright © 2011 Elsevier Ltd. All rights reserved.

  5. Carbocyclization versus oxycyclization on the metal-catalyzed reactions of oxyallenyl C3-linked indoles.

    Science.gov (United States)

    Alcaide, Benito; Almendros, Pedro; Alonso, José M; Fernández, Israel

    2013-07-05

    The preparation of previously unknown (indol-3-yl)-α-allenols and -allenones was accomplished from indole-3-carbaldehydes, through indium-mediated Barbier allenylation reaction taking advantage of the N-(2-pyridyl)sulfonyl group. Metal-catalyzed cyclizations of oxyallenyl C3-linked indoles proceeded in two ways depending on the presence or absence of the N-(2-pyridyl)sulfonyl group. For allenols, gold-catalyzed oxycyclization occurred in the presence of the protecting group; in the absence of the protecting group, palladium- and gold-catalyzed benzannulations operated. On the contrary, under gold catalysis furyl-indoles were obtained as exclusive products from NH-allenones, while 5-endo carbocyclization adducts were the major components starting from N-SO2py-protected allenones. These cyclization reactions have been developed experimentally, and their mechanisms have additionally been investigated by a computational study.

  6. Pyrolysis of Polyolefins Using Rotating Arc Plasma Technology for Production of Acetylene

    Directory of Open Access Journals (Sweden)

    Ming Zhang

    2017-04-01

    Full Text Available Polyolefin, as one of the most widely used macromolecule materials, has been one of the most serious threats to the environment. Current treatment methods of waste polyolefin including landfill, incineration, and thermal degradation have suffered from severe problems such as secondary pollution and the generation of other toxic substances. In this article, we report for the first time a high-efficiency method to produce high-value C2H2 from polyolefins using a rotating direct current arc plasma reactor, using polyethylene and polypropylene as feedstocks. The essence of this method is that a reductive atmosphere of pyrolysis enables a thermodynamic preference to C2H2 over other carbon-containing gas and the rotating direct current arc plasma reactor allows for a uniform distribution of high temperature to ensure high conversion of polymers. Thermodynamic simulation of product composition was performed, and the effect of plasma input power, polyolefin feed rate, and working gas flow rate on the pyrolysis results was experimentally investigated. It was found that, with proper parameter control, approximately complete conversion of carbon in polyolefin could be obtained, with a C2H2 selectivity higher than 80% and a C2H2 yield higher than 70%. These results not only create new opportunities for the reuse of polymer waste, but are also instructive for the green production of C2H2.

  7. Radiation degradation of poly(olefin sulphone)s - Fundamental research to practical applications

    International Nuclear Information System (INIS)

    Bowden, M.J.; O'Donnell, J.H.

    1985-01-01

    The degradation of poly(olefin sulphone)s by high energy radiation, particularly by γ-rays and electron beams, provides an example of the application of fundamental science to high technology industry. Scientific interest in the radiation degradation of these polymers was first aroused by the discovery that they underwent highly specific bond scission in the backbone chain as the primary result of absorption of high energy radiation and in fact they were the first polymers in which such an effect had been demonstrated. This conclusion was initially based mainly on evidence from electron spin resonance spectroscopy and was subsequently verified by studies of molecular weight changes. These studies showed that the poly(olefin sulphone)s not only degraded by main chain scission but were also among the most radiation-sensitive polymers known. The extremely high sensitivity of poly(olefin sulphone)s to radiation-induced main-chain scission has found application in the field of microelectronics. Electron beam writing on poly(olefin sulphone) films is used to produce lithographic masks for the manufacture of integrated circuits on silicon wafers. Poly(1-butene sulphone) (PBS) is currently used in the production of a substantial proportion of the masks for the industry. The fundamental aspects of the radiation degradation of poly(olefin sulphone)s and the practical applications to high technology are reviewed. (author)

  8. High-temperature migration of antioxidants from polyolefins.

    Science.gov (United States)

    Goydan, R; Schwope, A D; Reid, R C; Cramer, G

    1990-01-01

    Migration rates of radiolabelled antioxidants, Irganox-1010 (I-1010) and Irganox-1076 (I-1076), were measured from low- and high-density polyethylenes (LDPE, HDPE) and polypropylene (PP) at temperatures up to 135 degrees C. Water, 8 and 95 per cent aqueous ethanol and corn oil were employed as food simulating liquids (FSL). The experiments were conducted in a high-pressure cell in a manner that allowed contact between the polyolefin plaque and the FSL only during the test period and not while being heated. The migrations of the antioxidants varied with the square root of time, and the Fickian diffusion coefficients could be correlated with temperature in an Arrhenius fashion. Under comparable test conditions, antioxidant migrations were largest from PP for aqueous simulants, but for non-aqueous simulants the highest losses were from LDPE. In both instances lowest losses were from HDPE. In most instances there was little difference between the migration behaviour of I-1010 and I-1076. A few tests were conducted to measure the antioxidant migrations to foods. The losses were usually larger than those to water but below those to corn oil.

  9. Functionalization, Compatibilization and Properties of Polyolefin Composites with Natural Fibers

    Directory of Open Access Journals (Sweden)

    Vera Alvarez

    2010-11-01

    Full Text Available The article is focused on analyzing the effect of functionalization and reactive processing on the morphological, thermal, rheological and mechanical properties of composites of isotactic polypropylene (PP, polystyrene (PS, poly(ethylene-vinyl acetate (EVA, with cellulose fibers, hemp or oat as natural fillers. Both polymers and fibers were modified with bi-functional monomers (glycidyl methacrylate, GMA; maleic anhydride, MA capable of facilitating chemical reactions between the components during melt mixing. Polyolefin copolymers containing reactive groups (PP-g-GMA, SEBS-g-MA, PS-co-MA, etc. were used as compatibilizers. Optical and SEM microscopy, FTIR, RX, DSC, TGA, DMTA, rheological and mechanical tests were employed for the composites characterization. The properties of binary and ternary systems have been analyzed as a function of both fiber and compatibilizer content. All compatibilized systems showed enhanced fiber dispersion and interfacial adhesion. The phase behavior and the thermal stability of the composites were affected by the chemical modification of the fibers. Marked changes in the overall crystallization processes and crystal morphology of PP composites were observed owing to the nucleating effect of the fibers. The tensile mechanical behavior of the compatibilized composites generally resulted in a higher stiffness, depending on the fiber amount and the structure and concentration of compatibilizer.

  10. Biomimetic superhydrophobic polyolefin surfaces fabricated with a facile scraping, bonding and peeling method

    Directory of Open Access Journals (Sweden)

    Feng Huanhuan

    2016-01-01

    Full Text Available Inspired by the superhydrophobicity of juicy peach surface, on which microscale hairs are standing vertically to the surface plane, an extremely simple, inexpensive physical method is developed for fabrication of superhydrophobic polyolefin surfaces over large areas. This method includes three steps: abrasive paper scraping, adhesive tape bonding and 90° peeling. Scraping increases the roughness and enhence water contact angles (CAs on polyolefin surfaces. It increases more when the scraped surface are bonded with adhesive types and then then 90° peeled. The CA variation depends on the types of polyolefin and abrasive paper. Superhydrophobic lowdensity polyethylene (LDPE, high-density polyethylene (HDPE and polypropylene (PP surfaces (CA>150° are obtained and they all exhibit very low adhesive force and high resistance to strong acids and bases.

  11. Synthesis and antiviral activity of cyclopropyl-spirocarbocyclic adenosine, (4R,5S,6R,7R)-4-(6-amino-9H-purin-9-yl)-7-(hydroxymethyl)spiro[2.4]heptane-5,6-diol against hepatitis C virus.

    Science.gov (United States)

    Gadthula, Srinivas; Rawal, Ravindra K; Sharon, Ashoke; Wu, Dong; Korba, Brent; Chu, Chung K

    2011-07-01

    An efficient method was developed for the synthesis of 6-exocyclic methylene carbocyclic intermediate 4. The Simmons-Smith cyclopropanation protocol was applied on the 6-exocyclic methylene of intermediate 4 and demonstrated its utility for the synthesis of novel class of a spiro-carbocyclic nucleoside analog 8. The titled compound 8 demonstrated a significant antiviral activity against HCV with EC(50) values of 0.273 and 0.368 μM in genotypes 1A and 1B, respectively. Copyright © 2011 Elsevier Ltd. All rights reserved.

  12. Stability of sodium bicarbonate solutions in polyolefin bags.

    Science.gov (United States)

    Wear, Jennifer; McPherson, Timothy B; Kolling, William M

    2010-06-15

    The stability of sodium bicarbonate solutions in sterile water for injection or 5% dextrose injection stored at 21-24 degrees C or 2-4 degrees C was evaluated. Sodium bicarbonate injection was obtained in 50-mL vials of 8.4% (1 meq/mL). A total of 50, 100, or 150 meq of sodium bicarbonate was added to each 1-L polyolefin bag of either sterile water for injection or 5% dextrose injection. All solutions were prepared in a laminar-airflow hood using aseptic technique. Bags were punctured once to remove headspace air and once for the addition of each 50 meq of sodium bicarbonate. Six replicates of each test solution were prepared. The solutions were stored at 21-24 degrees C and 2-4 degrees C. Control solutions (50 and 150 meq) were similarly prepared in triplicate. Control solutions were sparged with either nitrogen gas or oxygen gas before storage. Sodium bicarbonate stability was assessed by measuring solution pH. Bicarbonate content was measured utilizing titration. Both pH and bicarbonate concentrations were measured immediately upon preparation and on days 3, 5, and 7 for both test and control solutions. All 95% confidence interval values for sample solution pH remained within 7.0-8.5 for seven days at 2-4 degrees C. Sodium bicarbonate solutions of 50, 100, and 150 meq in sterile water for injection or 5% dextrose injection were stable for up to seven days when refrigerated. The 50-meq solution was stable for up to 48 hours when stored at room temperature, and the 100- and 150-meq solutions were stable for up to 30 hours when stored at room temperature.

  13. Biomimetic superhydrophobic polyolefin surfaces fabricated with a facile scraping, bonding and peeling method

    NARCIS (Netherlands)

    Feng, Huanhuan; Zheng, Tingting; Wang, Huiliang

    2016-01-01

    Inspired by the superhydrophobicity of juicy peach surface, on which microscale hairs are standing vertically to the surface plane, an extremely simple, inexpensive physical method is developed for fabrication of superhydrophobic polyolefin surfaces over large areas. This method includes three

  14. The Influence of Ziegler-Natta and Metallocene Catalysts on Polyolefin Structure, Properties, and Processing Ability

    NARCIS (Netherlands)

    Shamiri, A.; Chakrabarti, M.H.; Jahan, S.; Hussain, M.A.; Kaminsky, W.; Aravind, P.V.; Yehye, W.A.

    2014-01-01

    50 years ago, Karl Ziegler and Giulio Natta were awarded the Nobel Prize for their discovery of the catalytic polymerization of ethylene and propylene using titanium compounds and aluminum-alkyls as co-catalysts. Polyolefins have grown to become one of the biggest of all produced polymers. New

  15. Characterization of post-consumer polyolefin wastes by hyperspectral imaging for quality control in recycling processes.

    Science.gov (United States)

    Serranti, Silvia; Gargiulo, Aldo; Bonifazi, Giuseppe

    2011-11-01

    In this paper new analytical inspection strategies, based on hyperspectral imaging (HSI) in the VIS-NIR and NIR wavelength ranges (400-1000 and 1000-1700 nm, respectively), have been investigated and set up in order to define quality control logics that could be applied at industrial plant level for polyolefins recycling. The research was developed inside the European FP7 Project W2Plastics "Magnetic Sorting and Ultrasound Sensor Technologies for Production of High Purity Secondary Polyolefins from Waste". The main aim of the project is the separation of pure polyethylene and polypropylene adopting an innovative process, the magnetic density separation (MDS). Spectra of plastic particles and contaminants resulting from post-consumer complex wastes and of virgin polyolefins have been acquired by HSI and by Raman spectroscopy. The classification results obtained applying principal component analysis (PCA) on HSI data have been compared with those obtained by Raman spectroscopy, in order to validate the proposed innovative methodology. Results showed that HSI sensing techniques allow to identify both polyolefins and contaminants. Results also demonstrated that HSI has a great potentiality as a tool for quality control of feed (identification of contaminants in the plastic waste) and of the two different pure polypropylene and polyethylene flow streams resulting from the MDS-based recycling process. Copyright © 2011 Elsevier Ltd. All rights reserved.

  16. Migration of antioxidant additives from various polyolefinic plastics into oleaginous vehicles.

    Science.gov (United States)

    Marcato, B; Guerra, S; Vianello, M; Scalia, S

    2003-05-12

    The migration of the antioxidant additives pentaerythrityl tetrakis(3,5-di-tert-butyl-4-hydroxyphenyl)propionate (Irganox 1010) and tris(2,4-di-tert-butylphenyl)phosphite (Irgafos 168) from polyolefinic packaging into oily vehicles was investigated. The polyolefins included in the study were from the following classes: isotactic polypropylene homopolymer (PP), ethylene-co-propylene random copolymer (RACO), ethylene-propylene heterophasic copolymer and ethylene-propylene amorphous copolymer blend (EP) and high-density polyethylene (HDPE). Each polymer was additioned with Irganox 1010 (0.15%, w/w) and Irgafos 168 (0.15%, w/w) and processed into blown bottles. To study the antioxidant release process, plastic sheets were cut from the bottles and dipped for various time intervals into a mixture of five oils (caprylic/capric triglyceride, cyclomethicone, dicaprylyl ether, isohexadecane and C(12-15) alkyl benzoate) representative of lipophilic excipients used in pharmaceutical and cosmetic formulations. After exposure to the oil medium, the non-migrated Irganox 1010 and Irgafos 168 were recovered from the polymeric matrices using microwave-assisted extraction with ethyl acetate-hexane and assayed by HPLC. The leaching of the two antioxidants varied remarkably depending on the polyolefin crystallinity and structure. The amount of Irganox 1010 transferred into the contact medium at 25 degrees C decreased in the order EP>RACO>PP>HDPE. The same polyolefin ranking was observed in the case of Irgafos 168, except for PP and HDPE which exhibited similar depletion of this additive. Migration of Irgafos 168 was greater than that of Irganox 1010 and the release of both antioxidants increased at higher temperature (50 degrees C). The obtained data are useful for the selection of polyolefinic matrices as raw-materials for the production of pharmaceutical and cosmetic containers.

  17. Essential work of fracture (EWF): a useful tool for the fracture toughness characterization of particulate polyolefin composites

    OpenAIRE

    Arencón Osuna, David; Antunes, Marcelo de Sousa Pais; Velasco Perero, José Ignacio

    2011-01-01

    The characterization of the fracture toughness of polyolefin composites filled with inorganic particles is commonly solved by means of standardized testing procedures based wherther on the Linear Elastic Fracture Mechanics (LEFM) and the Elastic-Plastic Fracture Mechanics approaches. Fracture parameters as Kc, Gc and Jc are obtained and managed as "material" parameters in plain strain conditions. Nevertheless, particulate polyolefin composites are often in form of film or sheet, making diffi...

  18. Oxygen permeability of nanocomposite-based polyolefin films; Permeabilidade do oxigenio em filmes nanocompositos poliolefinicos

    Energy Technology Data Exchange (ETDEWEB)

    Fujiyama-Novak, Jane H.; Amaral, Rafael A.; Ruffino, Vivianne; Habert, A. Claudio; Borges, Cristiano P., E-mail: jane@peq.coppe.ufrj.br [Coordenacao dos Programas de Pos-Graduacao em Engenharia (PEQ/COPPE/UFRJ), Rio de Janeiro, RJ (Brazil); Mano, Barbara [BRASKEM S.A., Duque de Caxias, RJ (Brazil)

    2015-07-01

    Polyethylene and polypropylene are vastly employed for packaging due to their high versatility and low cost. However, their films are permeable at different degree to small molecules like gases and the use of additives improves the barrier properties. Therefore, the aim of this work is to investigate the effect of organically modified montmorillonite on oxygen transport properties of PE and PP films. Nanocomposites were prepared by means of polymer dissolution in organic solvent and subsequent nanoparticle addition at 3, 5 and 10% (w/w). Scanning electron microscopy images of the films indicate the presence of microcavities and some agglomerated nanoclay. On the other hand, X-rays diffraction analysis shows clay in well-dispersed state independent of polyolefin type. Enhancement of oxygen barrier is achieved, but this property is dependent on the nanoclay content, polyolefin type and film morphology. (author)

  19. On crack propagation in the welded polyolefin pipes with and without the presence of weld beads

    Czech Academy of Sciences Publication Activity Database

    Mikula, Jakub; Hutař, Pavel; Nezbedová, E.; Lach, R.; Arbeiter, F.; Ševčík, Martin; Pinter, G.; Grellmann, W.; Náhlík, Luboš

    2015-01-01

    Roč. 87, DEC (2015), s. 95-104 ISSN 0264-1275 R&D Projects: GA ČR(CZ) GAP108/12/1560; GA MŠk(CZ) EE2.3.30.0063; GA MŠk(CZ) ED1.1.00/02.0068 Institutional support: RVO:68081723 Keywords : Slow crack growth * Butt weld * Lifetime estimation * Polyolefin pipes * Weld bead Subject RIV: JL - Materials Fatigue, Friction Mechanics Impact factor: 3.997, year: 2015

  20. Study of Polyolefines Waste Thermo-Destruction in Large Laboratory and in Industrial Installations

    Science.gov (United States)

    2014-12-15

    century in Poland, processes of thermal destruction of used polyolefines were carried out in vertical modular installations, using bauxite as the catalyst...catalytic process, for the elimination of the majority of deficiencies observed in plants utilizing bauxite as the catalyst, as well as the...hydrocarbons from the degradation of plastics”, Krakow, 2001. [20] Academy of Mining and Metallurgy in Krakow, “The research of energetic properties of the

  1. Stability of cyclosporine solutions stored in polypropylene-polyolefin bags and polypropylene syringes.

    Science.gov (United States)

    Li, Mengqing; Forest, Jean-Marc; Coursol, Christian; Leclair, Grégoire

    2011-09-01

    The stability of cyclosporine diluted to 0.2 or 2.5 mg/mL with 0.9% sodium chloride injection or 5% dextrose injection and stored in polypropylene-polyolefin containers or polypropylene syringes was evaluated. Intravenous cyclosporine solutions (0.2 and 2.5 mg/mL) were aseptically prepared and transferred to 250-mL polypropylene-polyolefin bags or 60-mL polypropylene syringes. Chemical stability was measured using a stability-indicating high-performance liquid chromatography (HPLC) assay. Physical stability was assessed by visual inspection and a dynamic light scattering (DLS) method. After 14 days, HPLC assay showed that the samples of i.v. cyclosporine stored in polypropylene-polyolefin bags remained chemically stable (>98% of initial amount remaining); the physical stability of the samples was confirmed by DLS and visual inspection. The samples stored in polypropylene syringes were found to contain an impurity (attributed to leaching of a syringe component by the solution) that could be detected by HPLC after 1 day; on further investigation, no leaching was detected when the syringes were exposed to undiluted i.v. cyclosporine 50 mg/mL for 10 minutes. Samples of i.v. cyclosporine solutions of 0.2 and 2.5 mg/mL diluted in 0.9% sodium chloride injection or 5% dextrose injection and stored at 25 °C in polypropylene-polyolefin bags were physically and chemically stable for at least 14 days. When stored in polypropylene syringes, the samples were contaminated by an impurity within 1 day; however, the short-term (i.e., ≤10 minutes) use of the syringes for the preparation and transfer of i.v. cyclosporine solution is considered safe.

  2. Influence of radiative irradiation on structure and physical-mechanical properties of polyolefins

    International Nuclear Information System (INIS)

    Kakhramanov, N.T.; Mamedova, N.A.; Gasanova, A.A.

    2014-01-01

    Full text : Today in the world it is synthesized a large number of polymer materials, which in one or another way satisfy the requirements for plastic construction products used in the various branches of industry and agriculture. In this work the main attention is paid to investigation of influence of radiative irradiation dose on structural peculiarities and basic physical-mechanical characteristics of cross-linked polyolefins

  3. Stability of levothyroxine injection in glass, polyvinyl chloride, and polyolefin containers.

    Science.gov (United States)

    Frenette, Anne Julie; MacLean, Robert D; Williamson, David; Marsolais, Pierre; Donnelly, Ronald F

    2011-09-15

    The 24-hour stability of a levothyroxine solution admixed and stored in three common infusion containers and infused through polyvinyl chloride (PVC) tubing was evaluated. Levothyroxine sodium 1-μg/mL injection prepared in glass bottles and PVC and polyolefin bags were assayed using high-performance liquid chromatography at 0, 1, 3, 6, 12, and 24 hours; samples drawn directly from the containers, as well as from the distal end of attached PVC tubing, were assayed. The area under the time-versus-concentration curve (AUC) for predicted and delivered doses was calculated; analysis of variance was used for comparison of the percentages of predicted and actual AUC values. The levothyroxine concentration was stable in glass bottles and polyolefin bags through 24 hours (mean ± S.D. percentage of initial concentration remaining, 103.5% ± 2.5% and 100.0% ± 2.9%, respectively). In the PVC infusion bags, the amount of drug decreased to 90% of the initial concentration within 1 hour and then rose and remained within acceptability limits. The levothyroxine concentration of the samples infused through PVC line from glass and polyolefin containers decreased after 1 hour by about 13%; the loss of the drug from the samples infused from PVC bags was higher (18%), presumably due to additive adsorptive effects. In all samples tested, the drug concentration rebounded and remained above 90% to the end of the study. Levothyroxine sodium 1-μg/mL solution was stable for 24 hours in glass bottles and polyolefin bags but when stored in PVC bags, the concentration decreased by 10% after 1 hour.

  4. Mechanistic Exploration of the Competition Relationship between a Ketone and C═C, C═N, or C═S Bond in the Rh(III)-Catalyzed Carbocyclization Reactions.

    Science.gov (United States)

    Xing, Yang-Yang; Liu, Jian-Biao; Sun, Chuan-Zhi; Huang, Fang; Chen, De-Zhan

    2018-04-02

    The introduction of a C═O, C═C, C═S, or C═N bond has emerged as an effective strategy for carbocycle synthesis. A computational mechanistic study of Rh(III)-catalyzed coupling of alkynes with enaminones, sulfoxonium ylides, or α-carbonyl-nitrones was carried out. Our results uncover the roles of dual directing groups in the three substrates and confirm that the ketone acts as the role of the directing group while the C═C, C═N, or C═S bond serves as the cyclization site. By comparing the coordination of the ketone versus the C═C, C═N, or C═S bond, as well as the chemoselectivity concerning the six- versus five-membered formation, a competition relationship is revealed within the dual directing groups. Furthermore, after the alkyne insertion, instead of the originally proposed direct reductive elimination mechanism, the ketone enolization is found to be essential prior to the reductive elimination. The following C(sp 2 )-C(sp 2 ) reductive elimination is more favorable than the C(sp 3 )-C(sp 2 ) formation, which can be explained by the aromaticity difference in the corresponding transition states. The substituent effect on controlling the selectivity was also discussed.

  5. Material recycling of post-consumer polyolefin bulk plastics: Influences on waste sorting and treatment processes in consideration of product qualities achievable.

    Science.gov (United States)

    Pfeisinger, Christian

    2017-02-01

    Material recycling of post-consumer bulk plastics made up of polyolefins is well developed. In this article, it is examined which effects on waste sorting and treatment processes influence the qualities of polyolefin-recyclats. It is shown that the properties and their changes during the product life-cycle of a polyolefin are defined by its way of polymerisation, its nature as a thermoplast, additives, other compound and composite materials, but also by the mechanical treatments during the production, its use where contact to foreign materials is possible and the waste sorting and treatment processes. Because of the sum of the effects influencing the quality of polyolefin-recyclats, conclusions are drawn for the material recycling of polyolefins to reach high qualities of their recyclats. Also, legal requirements like the EU regulation 1907/2006 concerning the registration, evaluation, authorisation and restrictions on chemicals are considered.

  6. Phosphine-catalyzed synthesis of 3,3-spirocyclopenteneoxindoles from γ-substituted allenoates: systematic studies and targeted applications.

    Science.gov (United States)

    Gomez, Catherine; Gicquel, Maxime; Carry, Jean-Christophe; Schio, Laurent; Retailleau, Pascal; Voituriez, Arnaud; Marinetti, Angela

    2013-02-15

    The phosphine-promoted [3 + 2] cyclizations between γ-substituted allenoates and arylideneoxindoles have been applied to the stereoselective synthesis of spiro(cyclopentene)oxindoles with trisubstituted cyclopentene units. It has been demonstrated that PPh(3) operates a very efficient control of the relative stereochemistry of the three stereogenic centers of the final spiranic products. Focused experiments have been carried out then so as to access carbocyclic analogues of an important series of anticancer agents inhibiting MDM2-p53 interactions.

  7. Evaluation of oxidative behavior of polyolefin geosynthetics utilizing accelerated aging tests based on temperature and pressure

    Science.gov (United States)

    Li, Mengjia

    Polyolefin geosynthetics are susceptible to oxidation, which eventually leads to the reduction in their engineering properties. In the application of polyolefin geosynthetics, a major issue is an estimate of the materials durability (i.e. service lifetime) under various aging conditions. Antioxidant packages are added to the polyolefin products to extend the induction time, during which antioxidants are gradually depleted and polymer oxidation reactions are prevented. In this PhD study, an improved laboratory accelerating aging method under elevated and high pressure environments was applied to evaluate the combined effect of temperature and pressure on the depletion of the antioxidants and the oxidation of polymers. Four types of commercial polyolefn geosynthetic materials selected for aging tests included HDPE geogrid, polypropylene woven and nonwoven geotextiles. A total of 33 different temperature/pressure aging conditions were used, with the incubation duration up to 24 months. The applied oven temperature ranged from 35°C to 105°C and the partial oxygen pressure ranged from 0.005 MPa to 6.3 MPa. Using the Oxidative Induction Time (OIT) test, the antioxidant depletion, which is correlated to the decrease of the OIT value, was found to follow apparent first-order decay. The OIT data also showed that, the antioxidant depletion rate increased with temperature according to the Arrhenius equation, while under constant temperatures, the rate increased exponentially with the partial pressure of oxygen. A modified Arrhenius model was developed to fit the antioxidant depletion rate as a function of temperature and pressure and to predict the antioxidant lifetime under various field conditions. This study has developed new temperature/pressure incubation aging test method with lifetime prediction models. Using this new technique, the antioxidant lifetime prediction results are close to regular temperature aging data while the aging duration can be reduced considerably

  8. Fused 1,2,3-Dithiazoles: Convenient Synthesis, Structural Characterization, and Electrochemical Properties

    Directory of Open Access Journals (Sweden)

    Lidia S. Konstantinova

    2016-05-01

    Full Text Available A new general protocol for synthesis of fused 1,2,3-dithiazoles by the reaction of cyclic oximes with S2Cl2 and pyridine in acetonitrile has been developed. The target 1,2,3-dithiazoles fused with various carbocycles, such as indene, naphthalenone, cyclohexadienone, cyclopentadiene, and benzoannulene, were selectively obtained in low to high yields. In most cases, the hetero ring-closure was accompanied by chlorination of the carbocyclic moieties. With naphthalenone derivatives, a novel dithiazole rearrangement (15→13 featuring unexpected movement of the dithiazole ring from α- to β-position, with respect to keto group, was discovered. Molecular structure of 4-chloro-5H-naphtho[1,2-d][1,2,3]dithiazol-5-one 13 was confirmed by single-crystal X-ray diffraction. Electrochemical properties of 13 were studied by cyclic voltammetry and a complex behavior was observed, most likely including hydrodechlorination at a low potential.

  9. The Influence of Ziegler-Natta and Metallocene Catalysts on Polyolefin Structure, Properties, and Processing Ability

    Directory of Open Access Journals (Sweden)

    Ahmad Shamiri

    2014-07-01

    Full Text Available 50 years ago, Karl Ziegler and Giulio Natta were awarded the Nobel Prize for their discovery of the catalytic polymerization of ethylene and propylene using titanium compounds and aluminum-alkyls as co-catalysts. Polyolefins have grown to become one of the biggest of all produced polymers. New metallocene/methylaluminoxane (MAO catalysts open the possibility to synthesize polymers with highly defined microstructure, tacticity, and steroregularity, as well as long-chain branched, or blocky copolymers with excellent properties. This improvement in polymerization is possible due to the single active sites available on the metallocene catalysts in contrast to their traditional counterparts. Moreover, these catalysts, half titanocenes/MAO, zirconocenes, and other single site catalysts can control various important parameters, such as co-monomer distribution, molecular weight, molecular weight distribution, molecular architecture, stereo-specificity, degree of linearity, and branching of the polymer. However, in most cases research in this area has reduced academia as olefin polymerization has seen significant advancements in the industries. Therefore, this paper aims to further motivate interest in polyolefin research in academia by highlighting promising and open areas for the future.

  10. The Influence of Ziegler-Natta and Metallocene Catalysts on Polyolefin Structure, Properties, and Processing Ability

    Science.gov (United States)

    Shamiri, Ahmad; Chakrabarti, Mohammed H.; Jahan, Shah; Hussain, Mohd Azlan; Kaminsky, Walter; Aravind, Purushothaman V.; Yehye, Wageeh A.

    2014-01-01

    50 years ago, Karl Ziegler and Giulio Natta were awarded the Nobel Prize for their discovery of the catalytic polymerization of ethylene and propylene using titanium compounds and aluminum-alkyls as co-catalysts. Polyolefins have grown to become one of the biggest of all produced polymers. New metallocene/methylaluminoxane (MAO) catalysts open the possibility to synthesize polymers with highly defined microstructure, tacticity, and steroregularity, as well as long-chain branched, or blocky copolymers with excellent properties. This improvement in polymerization is possible due to the single active sites available on the metallocene catalysts in contrast to their traditional counterparts. Moreover, these catalysts, half titanocenes/MAO, zirconocenes, and other single site catalysts can control various important parameters, such as co-monomer distribution, molecular weight, molecular weight distribution, molecular architecture, stereo-specificity, degree of linearity, and branching of the polymer. However, in most cases research in this area has reduced academia as olefin polymerization has seen significant advancements in the industries. Therefore, this paper aims to further motivate interest in polyolefin research in academia by highlighting promising and open areas for the future. PMID:28788120

  11. Output-oriented analysis of the wet mechanical processing of polyolefin-rich waste for feedstock recycling.

    Science.gov (United States)

    Kranzinger, Lukas; Pomberger, Roland; Schwabl, Daniel; Flachberger, Helmut; Bauer, Markus; Lehner, Markus; Hofer, Wolfgang

    2018-03-01

    In recent years, an increasing number of studies have revealed that plastics and their components (e.g. plasticisers) pose an environmental risk. However, it is hard to imagine how our industrialised society could do without these materials, since the fields of application are manifold. One possible approach to tackle this mounting problem is the implementation of a comprehensive and well-functioning collection and recycling system. An international comparison shows that only a small proportion of the total plastics in circulation is collected and recycled. The investigations conducted under the present research project, 'Plastic Reborn', focused on both identification and analysis of the discharge paths of polyolefin-rich waste streams, under the Austrian waste management system. Another objective was determining the utilisation potential of the output fractions of these polyolefin-rich waste streams, generated from a wet mechanical processing pilot plant. Experiments have shown that the polyolefins are successfully separated from the waste streams and that a total polyolefin potential of 429,000 t y -1 remains unexploited in the Austrian waste management system. Thus, these separated plastic fractions can make a significant contribution to the implementation of the European Circular Economy Directive. The residual fractions meet the legal and company-specific requirements for their use as solid recovered fuels in co-combustion plants.

  12. Radical cascade cyclization of 1,n-enynes and diynes for the synthesis of carbocycles and heterocycles.

    Science.gov (United States)

    Xuan, Jun; Studer, Armido

    2017-07-17

    Carbo- and heterocycles are widely found in natural products, biologically active structures, medicinally relevant compounds, and in many other fine chemicals. The development of novel, general and efficient methods for their construction has therefore gained great interest in synthetic organic chemistry. Recently, radical chemistry has become a heavily investigated research field (a renaissance!). Along these lines, radical cascade cyclization of 1,n-enynes and diynes has emerged as a powerful strategy for the preparation of carbo- and heterocycles. In this review, we highlight recent advances in this rapidly growing area also focusing on reaction mechanisms.

  13. Effect of stabilization on the recycling of polyolefins in blow moulding

    Science.gov (United States)

    Pecora, L.; Diraddo, R. W.

    1993-03-01

    Extrusion blow molding experiments were conducted on two polyolefins to demonstrate two classes of degradation that occurs during the recycling or reprocessing of polymers. The two main degradation reactions that reduce product performance are chain scission and crosslinking. Polyethylene undergoes both chain scission and crosslinking, while polypropylene undergoes only chain scission. The degradation reactions cause a shift in the molecular weight distribution of the material in question. This material property shift generally affects parison swell and sag. The changes in parison formation behavior manifest themselves in the final blow molded part. The use of appropriate stabilizers can minimize these changes and render the final part acceptable. Also, the use of stabilization can allow an increase in the amount of recycled feedstock in the final product.

  14. Effect of Composition and Chain Length on χ Parameter of Polyolefin Blends: A Molecular Dynamics Study

    Science.gov (United States)

    Khare, Rajesh; Ravichandran, Ashwin; Chen, Chau-Chyun

    Polymer blends exhibit complex phase behavior which is governed by several factors including temperature, composition and molecular weight of components. The thermodynamics of polymer blends is commonly described using the χ parameter. While variety of experimental studies exist on identifying the factors affecting the χ parameter, a detailed molecular scale understanding of these is a topic of current research. We have studied the effect of blend composition and chain length on χ parameter values for two model polyolefin blends. The blends studied are: polyisobutylene (PIB)/polybutadiene (PBD) and polyethylene (PE)/atactic polypropylene (aPP). Molecular dynamics simulations in combination with the integral equation theory formalism proposed by Schweizer and Curro [Journal of Chemical Physics, 91, 5059 (1989)] are used to determine the χ parameter for these systems and thereby study the effect of blend composition and chain length. The resulting χ parameter values are explained in terms of the molecular structure of these polymeric systems.

  15. Metallocene-based polyolefin foams: effects of oxidative irradiation on mechanical properties

    International Nuclear Information System (INIS)

    Bhatt, Chinmay U.; Khan, Saad A.; Hwang, C. Robin

    1998-01-01

    Metallocene-based polyolefin (MPO) foams are being considered for a wide range of applications because of their uniform composition and low toxicity. In this study, stress relaxation and dynamic rheological experiments are used to probe the effects of oxidative irradiation on the structure and final properties of these novel MPO foams. Experiments conducted on irradiated foams of two different densities reveal significantly different behavior. Gamma irradiation of the lighter foam causes structural degradation due to chain scission reactions. This is manifested in faster stress relaxation rates and lower values of elastic moduli and gel fraction in the irradiated samples. The incorporation of O 2 into the polymer backbone, verified by FTIR analysis, confirms the hypothesis of chain scission occurring at the labile peroxide linkages. In contrast, the denser foam shows a small amount of cross-linking and a concomitant improvement in mechanical properties after oxidative irradiation

  16. Metallocene-based polyolefin foams: effects of oxidative irradiation on mechanical properties

    Energy Technology Data Exchange (ETDEWEB)

    Bhatt, Chinmay U.; Khan, Saad A. [Department of Chemical Engineering, North Carolina State University, Raleigh, NC (United States); Hwang, C. Robin [Becton Dickinson Technologies, Research Triangle Park, NC (United States)

    1998-11-01

    Metallocene-based polyolefin (MPO) foams are being considered for a wide range of applications because of their uniform composition and low toxicity. In this study, stress relaxation and dynamic rheological experiments are used to probe the effects of oxidative irradiation on the structure and final properties of these novel MPO foams. Experiments conducted on irradiated foams of two different densities reveal significantly different behavior. Gamma irradiation of the lighter foam causes structural degradation due to chain scission reactions. This is manifested in faster stress relaxation rates and lower values of elastic moduli and gel fraction in the irradiated samples. The incorporation of O{sub 2} into the polymer backbone, verified by FTIR analysis, confirms the hypothesis of chain scission occurring at the labile peroxide linkages. In contrast, the denser foam shows a small amount of cross-linking and a concomitant improvement in mechanical properties after oxidative irradiation.

  17. Effect of microstructure on the thermo-oxidation of solid isotactic polypropylene-based polyolefins

    Directory of Open Access Journals (Sweden)

    Mario Hoyos, Pilar Tiemblo and José Manuel Gómez-Elvira

    2008-01-01

    Full Text Available In the present work we aim to clarify the role of the microstructure and the crystalline distribution from the thermo-oxidation of solid isotactic PP (iPP and ethylene-propylene (EP copolymers. The effects of the content and quality of the isotacticity interruptions, together with the associated average isotactic length, on the induction time (ti as well as on the activation energy (Eact of the thermo-oxidation are analysed. Both parameters have been found to change markedly at an average isotactic length (n1 of 30 propylene units. While ti reaches a minimum when n1 is approximately 30 units, Eact increases quasi-exponentially as the number of units decreases from 30. This variation can be explained in terms of changes induced in the crystalline interphase, i.e. local molecular dynamics, which are closely linked to the initiation of the thermo-oxidation of isotactic PP-based polyolefins.

  18. Study on the cause of discoloration of radiation-exposed polyolefin

    Energy Technology Data Exchange (ETDEWEB)

    Jeun, Joonpyo; Kang, Philhyun; Oh, Seunghwan; Kim, Hyunbin

    2013-01-15

    Olefinic polymers, such as polyethylene and polypropylene, have a wide variety of known end use applications. Olefinic polymers have been disclosed to be useful in the manufacture of shaped articles for medical used and for food packaging uses where the articles must undergo stabilization for be disinfected. Notwithstanding the significant known advantages of sterilization by means of high energy radiation, several disadvantages are known to be associated with such sterilization techniques. Most of all, when treated with radiation energy in an amount sufficient to achieve the desired sterilization, such polyolefin compositions may become discolored. This coloration may occur for a variety of reasons such as the use of certain additives in the polymer, as well as the presence of high amounts of catalytic residues. In this study, effects of structure of antioxidant and UV stabilizer on the discoloration of olefinic polymer resin were investigated. Furthermore, The mechanism of discoloration of olefinic polymer was suggested.

  19. Electrochemical properties of polyolefine nonwoven fabric modified with carboxylic acid group for battery separator

    International Nuclear Information System (INIS)

    Choi, Seong-Ho; Park, Keung-Shik; Kang, Hae-Jeong; Ryu, Eun-Nyoung; Lee, Pill-Kwang

    2000-01-01

    Carboxylic acid group was introduced by radiation-induced grafting of acrylic acid (AAc) onto polyolefine nonwoven fabric (PNF), wherein the PNF comprises at least about 60% of a polyethylene having a melting temperature at ∼132degC and no more than about 40% of a second polypropylene having a lower melting temperature at ∼162degC, for a battery separator. The AAc-grafted PNF was characterized by XPS, SEM, DSC, TGA and porosimeter. The wetting speed, electrolyte retention, electrical resistance, and tensile strength were evaluated after grafting of AAc. It was found that the wetting speed, electrolyte retention, thickness, and ion-exchange capacity increased, whereas the electrical resistance decreased with increasing grafting yield. The tensile strength decreased with increasing grafting yield, whereas the elongation decreased with increasing grafting yield. (author)

  20. Electrochemical properties of polyolefin nonwoven fabric modified with carboxylic acid group for battery separator

    International Nuclear Information System (INIS)

    Choi, Seong-Ho; Kang, Hae-Jeong; Ryu, Eun-Nyoung; Lee, Kwang-Pill

    2001-01-01

    Carboxylic acid group was introduced by radiation-induced grafting of acrylic acid (AAc) onto polyolefine nonwoven fabric (PNF), wherein the PNF comprises at least about 60% of a polyethylene having a melting temperature at ∼132 deg. C and no more than about 40% of a second polypropylene having a lower melting temperature at ∼162 deg. C, for a battery separator. The AAc-grafted PNF was characterized by XPS, SEM, DSC, TGA and porosimeter. The wetting speed, electrolyte retention, electrical resistance, and tensile strength were evaluated after grafting of AAc. It was found that the wetting speed, electrolyte retention, thickness, and ion-exchange capacity increased, whereas the electrical resistance decreased with increasing grafting yield. The tensile strength decreased with increasing grafting yield, whereas the elongation decreased with increasing grafting yield. (author)

  1. Compatibility of ondansetron hydrochloride and methylprednisolone sodium succinate in multilayer polyolefin containers.

    Science.gov (United States)

    Bougouin, Christelle; Thelcide, Chloë; Crespin-Maillard, Fabienne; Maillard, Christian; Kinowski, Jean Marie; Favier, Mireille

    2005-10-01

    The compatibility of ondansetron hydrochloride and methylprednisolone sodium succinate in 5% dextrose injection and 0.9% sodium chloride injection was studied. Test solutions of ondansetron hydrochloride 0.16 mg/mL and methylprednisolone sodium succinate 2.4 mg/mL were prepared in triplicate and tested in duplicate. Total volumes of 4 and 2 mL of ondansetron hydrochloride solution and methylprednisolone sodium succinate solution, respectively, were added to 50-mL multilayer polyolefin bags containing 5% dextrose injection or 0.9% sodium chloride injection. Bags were stored for 24 hours at 20-25 degrees C and for 48 hours at 4-8 degrees C. Chemical compatibility was measured with high-performance liquid chromatography, and physical compatibility was determined visually. Ondansetron hydrochloride was stable for up to 24 hours at 20-25 degrees C and up to 48 hours at 4-8 degrees C. Methylprednisolone sodium succinate was stable for up to 48 hours at 4-8 degrees C. When stored at 20-25 degrees C, methylprednisolone sodium succinate was stable for up to 7 hours in 5% dextrose injection and up to 24 hours in 0.9% sodium chloride injection. Compatibility data for solutions containing ondansetron hydrochloride plus methylprednisolone sodium succinate revealed that each drug was stable for up to 24 hours at 20-25 degrees C and up to 48 hours at 4-8 degrees C. Ondansetron 0.16 mg/mL (as the hydrochloride) and methylprednisolone 2.4 mg/mL (as the sodium succinate) mixed in 50-mL multilayer polyolefin bags were stable in both 5% dextrose injection and 0.9% sodium chloride injection for up to 24 hours at 20-25 degrees C and up to 48 hours at 4-8 degrees C.

  2. Stability of 2 mg/mL Adenosine Solution in Polyvinyl Chloride and Polyolefin Infusion Bags.

    Science.gov (United States)

    DeAngelis, Michael; Ferrara, Alexander; Gregory, Kaleigh; Zammit, Kimberly; Zhao, Fang

    2018-04-01

    Adenosine is a potent endogenous mediator of vasodilation. Compounded sterile solutions of adenosine are used in cardiac catheterization lab to perform stress tests on the heart. These tests are used to determine the fractional flow reserve (FFR) and are commonly used in the management and diagnosis of cardiovascular conditions. The purpose of this study was to assess the physical and chemical stability of 2 mg/mL adenosine in 0.9% Sodium Chloride Injection, USP in polyvinyl chloride [PVC]) and polyolefin infusion bags stored at room temperature (20°C-25°C) and under refrigeration (2°C-8°C). The compounding and analytical methods used in this study were very similar to those described in the prior publications from the authors' laboratory. To ensure a uniform starting concentration of all stability samples, a batch of 2 mg/mL adenosine solution was prepared and then packaged into empty PVC and polyolefin infusion bags. These stability samples were prepared in triplicate for each bag type and storage temperature (a total of 12 samples). The infusion bag samples were assessed for stability immediately after preparation and after 1 day, 3 days, 7 days, and 14 days. At each time point, the infusion bags were first visually inspected against a light background for color change, clarity, and particulates. Aliquots were drawn from each sample at each time point for pH analysis and high-performance liquid chromatography (HPLC) analysis. Over 14 days of storage at room temperature or refrigeration, no considerable change in visual appearance or pH was observed in any bags. All samples retained 90% to 110% of the initial drug concentration. No significant degradation peaks were observed in the HPLC chromatograms.

  3. 2'-Fluoro-6'-methylene carbocyclic adenosine and its phosphoramidate prodrug: A novel anti-HBV agent, active against drug-resistant HBV mutants.

    Science.gov (United States)

    Singh, Uma S; Mulamoottil, Varughese A; Chu, Chung K

    2018-05-01

    Chronic hepatitis B (CHB) is one of the major causes of morbidity and mortality worldwide. Currently, clinically approved nucleos(t)ide analogs (NAs) are very efficient in reducing the load of hepatitis B virus (HBV) with minimum side effects. However, the long-term administration of antiviral drugs promotes HBV for potential drug resistance. To overcome this problem, combination therapies are administered, but HBV progressively altered mutations remain a threat. Therefore, optimally designed NAs are urgently needed to treat drug-resistant HBV. Herein, 2'-fluoro-6'-methylene carbocyclic adenosine (FMCA) and its phosphoramidate (FMCAP) have been discovered, which may be utilized in combination therapies for curing drug-resistant chronic hepatitis B. In preclinical studies, these carbocyclic NAs demonstrated potential anti-HBV activity against adefovir, as well as lamivudine (LMV/LAM) drug-resistant mutants. In vitro, these molecules have demonstrated significant activity against LMV/entecavir (ETV) triple mutants (L180M + S202G + M204V). Also, preliminary studies of FMCA/FMCAP in chimeric mice and female Non-obese diabetic/severe combined immunodeficiency (NOD/SCID) mouse models having the LMV/ETV triple mutant have shown a high rate of reduction of HBV DNA levels compared to ETV. In this review, we have summarized preclinical studies of FMCA and its phosphoramidate prodrug (FMCAP). © 2018 Wiley Periodicals, Inc.

  4. Propagation/depropagation equilibrium and structural factors in the radiation degradation of poly(olefin sulfone)s

    International Nuclear Information System (INIS)

    Bowmer, T.N.; O'Donnell, J.H.

    1981-01-01

    The principal volatile products observed after γ irradiation of nine different poly(olefin sulfone)s in the solid state were the two comonomers, i.e., the respective olefin and sulfur dioxide. An exponential increase in yield, G (volatile products), with increasing irradiation temperature, T/sub irr/, was observed for each copolymer through the ceiling temperature, T/sub c/, for the corresponding propagation/depropagation equilibrium. Thus the G value increased by ca. 3 orders of magnitude from T/sub irr/ = 0.7 T/sub c/ to T/sub irr/ = 1.3 T/sub c/ for all of the poly(olefin sulfone)s. Depropagation sensitivity was considered to be best measured by G(SO 2 ) since radiation induced, cationic homopolymerization of the product olefin occurred to a variable extent. Five of the poly(olefin sulfone)s had similar rates of depropagation at their respective T/sub c's/ but the polysulfones of 1-hexene, cyclohexene and 2-butene showed anomalously high depropagation rates. This may be related to greater steric hinderance to segmental chain mobility in the polysulfones of the 1,2 disubstituted olefins. Poly(1-hexene sulfone) appears to be anomalous, as in other respects

  5. Investigation of six-membered carbocyclic compounds as a molecular switch block of room temperature phosphorescence in nondeoxygenated β-cyclodextrin solution

    International Nuclear Information System (INIS)

    Zhang Hairong; Wei Yansheng; Jin Weijun; Liu Changsong

    2003-01-01

    An aerated aqueous solution, intense room temperature phosphorescence (RTP) of nitrogen heterocyclic compounds (NHCs) and polyaromatic hydrocarbons (PAHs) can be observed when micro amounts of six-membered carbocyclic compounds (6-MCCs) are introduced in β-cyclodextrin (β-CD) solution. In order to find the predominating factors of the enhanced phosphorescence observed with this novel approach, 22 typical phosphors of NHCs and PAHs were carefully screened and served as model compounds. The role of the inner heavy atom, the substituent group and the host-guest molecules space-matching on the RTP of different phosphors were investigated. The results demonstrated that the enhancement effects of cyclohexane, bromocyclohexane and cyclohexanol for the RTP of NHCs and PAHs have precedence over traditional halide alkanes such as 1,2-dibromoethane (DBE), exhibiting an obvious sequence as following: cyclohexane > bromocyclohexane > cyclohexanol. This new approach compared with other RTP methods is simple, convenient and fast

  6. Execution of a protocol for the supplier selection of a high density polyolefin

    International Nuclear Information System (INIS)

    Flores Pina, Lizette

    2013-01-01

    A new supplier of high-density polyolefin is selected for a medical industry, as a contingency plan in case the current provider presents problems of raw material supply. The Purchasing Department has coordinated the selection of the new resin supplier, providing high quality standards, deadlines and convenient price. The new resin obtained from the new provider was subjected to the protocol. The necessary tests were established for the comparison between the two resins (resin current and new resin). The tests were executed in a laboratory supported by the company in the United States. The tests most significant have corresponded to infrared Fourier transform tests, differential scanning calorimetry, melt flow rate and thermo gravimetry. Tests have defined the main characteristics of both resins with positive results and complying with the specifications set by the protocol. The two resins were established as such to be used in the production process of the product. Comparison phase of results are completely proceeding to execute the validation of the resin to run a test then preset design [es

  7. Channeling Polyolefin Molecular Structure - Bulk Property Correlation Strategies for Industrial Applicability

    Science.gov (United States)

    Hule, Rohan; Thurman, Derek; Doufas, Antonios

    Polyolefins occupy a significant volume of the polymer products portfolio in commodity and high value applications. Quantifying and optimizing structure-property relationships enables growth in new markets. It is well recognized that coupling lab-based, comprehensive methodologies with bulk properties of interest to industrial environments offer the greatest potential of technology advancement, ultimately leading to commercial success. It is imperative to recognize the existing gap of knowledge translation between lab measurements and industrial-scale operability. This study highlights experimental HDPEs synthesized from dual, single-site, co-supported catalysts that exhibit enhanced solid-state properties such as stiffness, impact and ESCR surpassing conventional trends. Commercial resins across distinct sub-families were included as well. Commonality amongst these resins is bimodality and broad MW distribution with well-defined splits and spreads. Investigations on commercially relevant parameters such as melt strength, melt elasticity and shear thinning established excellent performance for experimental bimodals, corroborating potential benefits compared to commercial HDPEs. To summarize, the effort highlights well-recognized pathways such as improvements in mechanical and melt properties that can be attributed to apposite tuning of polymer chain architecture and MW distribution with implications across myriad markets. Ultimately, this may serve as a pathway for producing innovative products that deliver business success and growth.

  8. Physico-chemical modification of polyolefins irradiated by swift heavy ions

    Science.gov (United States)

    Apel, P. Yu.; Didyk, A. Yu.; Salina, A. G.

    1996-02-01

    The physico-chemical modifications of polypropylene (PP) and polyethylene (PE) induced by 1 MeV/u Xe ions were studied. The irradiated samples were investigated ex situ by means of ultraviolet (UV) spectroscopy, solubility measurements and gel permeation chromatography (GPC). The formation of double bonds, dienes and trienes was observed both in PE and PP. The efficiency of the generation of unsaturated chemical bonds was found to depend on small amounts of aromatic additives in PP. Similarly, the track etch rate in PP increases with increasing concentration of antioxidant molecules. Rough estimates of radiolytic yields of different structures were carried out on the basis of the UV and GPC measurements. It is apparent that there are two basically different processes induced by swift heavy ions passing through the polyolefin: (a) local intratrack reactions; (b) reactions induced by active species leaving the tracks and diffusing into surrounding matrix. The former process leads to the formation of etchable damage. The latter one may cause a mutual influence of tracks even at fairly low ion fluences.

  9. Change of Mechanical Properties of Powder Recyclate Reinforced Polyolefin Based on Gamma Radiation

    Directory of Open Access Journals (Sweden)

    Yilmaz Kismet

    2017-08-01

    Full Text Available In this study, the changes observed in the mechanical properties of standard test specimens that were produced with powder coating reinforced polyolefin (polyethylene and polypropylene due to gamma radiation were examined. Matrix material of these specimens included low density polyethylene and polypropylene and 5%, 10%, 20%, 30%, 40% and 50% electrostatic powder coating waste by weight, and the samples were exposed to 44 kGry gamma-radiation for twenty four hours. Mechanical tests applied to the specimens after radiation demonstrated that the physical bonding mechanism between matrix material and filler material was reinforced. In the mechanical tests, tensile strength, three-point bending strength, and Izod impact strength of the samples were investigated and the results were compared to the results obtained in the mechanical tests when they were not radiated. Thus, the effects of gamma radiation on the mechanical properties of the filler material, and the electrostatic powder coating reinforced polyethylene and polypropylene were determined. Furthermore, section images of the radiated samples were taken with a scanning electron microscope and compared to the section images of irradiated samples to observe the physical bonding mechanism.

  10. Creep and Recovery Behaviour of Polyolefin-Rubber Nanocomposites Developed for Additive Manufacturing

    Directory of Open Access Journals (Sweden)

    Fugen Daver

    2016-12-01

    Full Text Available Nanocomposite application in automotive engineering materials is subject to continual stress fields together with recovery periods, under extremes of temperature variations. The aim is to prepare and characterize polyolefin-rubber nanocomposites developed for additive manufacturing in terms of their time-dependent deformation behaviour as revealed in creep-recovery experiments. The composites consisted of linear low density polyethylene and functionalized rubber particles. Maleic anhydride compatibilizer grafted to polyethylene was used to enhance adhesion between the polyethylene and rubber; and multi-walled carbon nanotubes were introduced to impart electrical conductivity. Various compositions of nanocomposites were tested under constant stress in creep and recovery. A four-element mechanistic Burger model was employed to model the creep phase of the composites, while a Weibull distribution function was employed to model the recovery phase of the composites. Finite element analysis using Abaqus enabled numerical modelling of the creep phase of the composites. Both analytical and numerical solutions were found to be consistent with the experimental results. Creep and recovery were dependent on: (i composite composition; (ii compatibilizers content; (iii carbon nanotubes that formed a percolation network.

  11. Stability of midazolam hydrochloride injection 1-mg/mL solutions in polyvinyl chloride and polyolefin bags.

    Science.gov (United States)

    Karlage, Kelly; Earhart, Zachary; Green-Boesen, Kelly; Myrdal, Paul B

    2011-08-15

    The stability of midazolam hydrochloride injection 1-mg/mL solutions in polyvinyl chloride (PVC) and polyolefin bags under varying conditions was evaluated. Triplicate solutions of midazolam hydrochloride 1-mg/mL were prepared in polyolefin and PVC i.v. bags by diluting midazolam hydrochloride injection 5 mg/mL with 5% dextrose injection. Bags were then stored under refrigeration (3-4 °C), exposed to light at room temperature (20-25 °C), or protected from light in amber bags at room temperature. Samples were taken immediately after preparation (day 0) and on days 1, 2, 3, 6, 13, 20, and 27 for analysis with a stability-indicating high-performance liquid chromatography assay in order to determine solution concentration. Stability was defined as retention of at least 90% of the initial drug concentration. The pH of each solution was also measured weekly. Sterility of the i.v. bags was determined at the end of the study by microbiological testing with culture in growth media. Differences in concentrations under the various storage conditions and bags used were analyzed using analysis of variance. All solutions retained over 98% of the initial midazolam hydrochloride concentration, with no statistically significant (p ≥ 0.05) change in concentration over the four-week period. Stability was not affected by temperature, exposure to light, or bag type. The pH of all solutions remained between 3.2 and 3.4 throughout the study. Sterility after 28 days was retained. Midazolam hydrochloride 1-mg/mL solutions diluted in 5% dextrose injection remained stable over 27 days in both polyolefin and PVC i.v. bags, regardless of storage condition.

  12. Compatibility of butorphanol with granisetron in 0.9% sodium chloride injection packaged in glass bottles or polyolefin bags.

    Science.gov (United States)

    Chen, Fu-Chao; Xiong, Hui; Liu, Hui-Min; Fang, Bao-Xia; Li, Peng

    2015-08-15

    The stability of admixtures containing butorphanol and granisetron in polyolefin bags and glass bottles stored at 4 and 25 °C was studied. Commercial solutions of butorphanol tartrate and granisetron hydrochloride were combined and further diluted with 0.9% sodium chloride injection to final concentrations of butorphanol tartrate 0.08 mg/mL and granisetron 0.03 or 0.06 mg/mL; the resulting mixtures were packaged in polyolefin bags and glass bottles. The admixtures were assessed for periods of up to 48 hours after storage at 25 °C without protection from room light and up to 14 days at 4 °C with protection from room light. The chemical stability of the admixtures was evaluated by a validated high-performance liquid chromatography (HPLC) method and by measurement of pH values. Solution appearance and color were assessed by observing the samples against room light and dark backgrounds. HPLC analysis demonstrated that the percentages of the initial concentrations of butorphanol and granisetron in the various solutions remained above 97% during the testing period. No changes in color or turbidity were observed in any of the prepared solutions. Throughout this period, pH values remained stable. Admixtures of butorphanol tartrate 0.08 mg/mL and granisetron 0.03 or 0.06 mg/mL in 0.9% sodium chloride injection in polyolefin bags or glass bottles remained stable for 48 hours when stored at 25 °C exposed to room light and for 14 days when stored at 4 °C protected from room light. Copyright © 2015 by the American Society of Health-System Pharmacists, Inc. All rights reserved.

  13. Potential environmental benefits of improving recycling of polyolefines – LCA of Magnetic density separation (MDS) developed in the EU FP7 funded project W2Plastic

    DEFF Research Database (Denmark)

    Olsen, Stig Irving; Bonou, Alexandra

    2012-01-01

    The core of the EU FP7 funded project W2Plastic is development of a magnetic density separation (MDS) of polyolefines in order to improve the sorting efficiency of these polymer types in different waste fractions. As part of the project a life cycle assessment is performed in order to firstly...... identify eco-design criteria for the development and secondly to document the potential environmental improvement of polyolefin recycling using the MDS technology. A preliminary study focusing solely on the carbon footprint benefits of recycling plastic waste compared to virgin production of polymers...

  14. Longterm performance of polyolefins in different environments including chlorinated water: antioxidant consumption and migration and polymer degradation

    OpenAIRE

    Lundbäck, Marie

    2005-01-01

    The long-term performance of stabilized polyolefins in different environments was studied with focus on antioxidant consumption and migration. Plaques of linear polyethylene (LPE) and branched polyethylene (BPE) were stabilized with Santonox® R (4,4'-Thiobis(6-tert-butyl-3-methylphenol)), Irganox® 1081 (2,2’-Thiobis(4-methyl-6-tertbutylphenol)), or Lowinox® 22M46 (2,2’-Methylenebis(6-tert-butyl-4-methylphenol)). The samples were aged in water and nitrogen at 75, 90 and 95°C. Antioxidant conce...

  15. Use of Taylor rod-on-anvil impact experiments to investigate high strain rate behavior in polyolefins

    Science.gov (United States)

    Luce, Amanda; Breidenich, Jennifer; Kannan, Abhiram; Thadhani, Naresh; Bucknall, David G.

    2017-01-01

    Taylor rod-on-anvil impact experiments have been performed on a range of polyolefins. At impact velocity greater than 250 m/s there are significant differences observed in the deformation behavior between the four polymers, which cannot be explained based on current understanding. During the initial stages of impact, mechno-luminescence is observed in all polymers and at all impact velocities. The location and length scale of this luminescence is consistent with the observed location of temperature increases that approach, and in some instances, exceed the melt point of the polymers.

  16. Effect of fungal decay on the hygroscopic thickness swelling rate of lignocellulosic filler-polyolefin biocomposites

    Science.gov (United States)

    Kord, B.; Hosseinihashemi, S. Kh.

    2014-01-01

    The influence of fungal decay on the hygroscopic thickness swelling rate of lignocellulosic filler-polyolefin biocomposites has been investigated. Composites based on polypropylene (PP), bagasse fiber (BF), and a coupling agent (PP-g-MA) were made by melt compounding and injection molding. The weigt ratio of BF to PP was controlled at 60/40 for all blends. The amount of coupling agent was fixed at 2% for all formulations. The samples obtained were exposed to the action of brown-rot (Coniophora puteana) and white-rot (Trametes versicolor) fungi for 8, 12, and 16 weeks according to the Kolle-flask method. The thickness swelling of the samples was evaluated by immersing them in water at room temperature for several weeks. The morphology of the composites was characterized using the scanning electron microscopy (SEM). The results indicated that the fungal decay had an adverse affect on the dimensional stability of BF/PP composites due to an increase in the thickness swelling rate. The thickness swelling of white-rotted samples was higher than that of brown-rotted ones and control samples. Also, the thickness swelling of BF/PP composites increased with increasing time of fungal decay. In addition, after 16 weeks of exposure to white-rot fungi, the composites exhibited a higher parameter of swelling rate K SR than control samples. The K SR of the composites was influenced both by the type of rooting and the exposure time. Furthermore, the SEM micrographs showed that the extent of degradation increased with growing exposure time to fungi.

  17. 2- and 3-Fluoro-3-deazaneplanocins, 2-fluoro-3-deazaaristeromycins, and 3-methyl-3-deazaneplanocin: Synthesis and antiviral properties.

    Science.gov (United States)

    Liu, Chong; Chen, Qi; Gorden, John D; Schneller, Stewart W

    2015-09-01

    The 3-deaza analogs of the naturally occurring adenine-based carbocyclic nucleosides aristeromycin and neplanocin possess biological properties that have not been optimized. In that direction, this paper reports the strategic placement of a fluorine atom at the C-2 and C-3 positions and a methyl at the C-3 site of the 3-deazaadenine ring of the aforementioned compounds. The synthesis and S-adenosylhomocysteine hydrolase inhibitory and antiviral properties of these targets are described. Some, but not all, compounds in this series showed significant activity toward herpes, arena, bunya, flavi, and orthomyxoviruses. Copyright © 2015 Elsevier Ltd. All rights reserved.

  18. Heterogeneous polymer modification: Polyolefin maleation in supercritical carbon dioxide and amorphous fluoropolymer surface modification

    Science.gov (United States)

    Hayes, Heather J.

    1999-11-01

    Three distinct heterogeneous polymer modification reactions are explored in this work. The first is a bulk reaction commonly conducted on polyolefins---the free radical addition of maleic anhydride. This reaction was run using supercritical carbon dioxide (SC CO2) as the solvent. The second was the chemical surface modification of an amorphous fluorocopolymer of tetrafluoroethylene and a perfluorodioxole monomer (Teflon AF). Several reactions were explored to reduce the surface of the fluorocopolymer for the enhancement of wettability. The last modification was also on Teflon AF and involved the physical modification of the surface through the transport polymerization of xylylene in order to synthesize a novel bilayer membrane. The bulk maleation of poly-4-methyl-1-pentene (PMP) was the focus of the first project. SC CO2 was utilized as both solvent and swelling agent to promote this heterogeneous reaction and led to successful grafting of anhydride groups on both PMP and linear low density polyethylene. Varying the reaction conditions and reagent concentrations allowed optimization of the reaction. The grafted anhydride units were found to exist as single maleic and succinic grafts, and the PMP became crosslinked upon maleation. The surface of a fluoropolymer can be difficult to alter. An examination of three reactions was made to determine the reactivity of Teflon AF: sodium naphthalenide treatment (Na-Nap), aluminum metal modification through deposition and dissolution, and mercury/ammonia photosensitization. The fluorocopolymer with the lower perfluorodioxole percentage was found to be more reactive towards modification with the Na-Nap treatment. The other modification reactions appeared to be nearly equally reactive toward both fluorocopolymers. The functionality of the Na-Nap-treated surface was examined in detail with the use of several derivatization reactions. In the final project, an asymmetric gas separation membrane was synthesized using Teflon AF as

  19. Metabolism of the carbocyclic analogue of (E)-5-(2-iodovinyl)-2'-deoxyuridine in herpes simplex virus-infected cells. Incorporation of C-IVDU into DNA

    International Nuclear Information System (INIS)

    De Clercq, E.; Bernaerts, R.; Balzarini, J.; Herdewijn, P.; Verbruggen, A.

    1985-01-01

    The carbocyclic analogues of (E)-5-(2-bromovinyl)-2'-deoxyuridine (BVDU) and (E)-5-(2-iodovinyl)-2'-deoxyuridine (IVDU), in which the sugar moiety is replaced by a cyclopentane ring and which have been designated as C-BVDU and C-IVDU, respectively, are, like their parent compounds BVDU and IVDU, potent and selective inhibitors of herpes simplex virus type 1 (HSV-1) and, to a lesser extent, herpes simplex virus type 2 (HSV-2) replication. The authors have now synthesized the radiolabeled C-IVDU analogue, C-[ 125 I]IVDU, and determined its metabolism by HSV-infected and mock-infected Vero cells. C-[ 125 I]IVDU was effectively phosphorylated by HSV-1-infected cells and, to a lesser extent, HSV-2-infected cells. C-[ 125 I]IVDU was not phosphorylated to an appreciable extent by either mock-infected cells or cells that had been infected with a thymidine kinase-deficient mutant of HSV-1. Furthermore, C-[ 125 I]IVDU was incorporated into both viral and cellular DNA of HSV-1-infected Vero cells. This finding represents the first demonstration of the incorporation of a cyclopentylpyrimidine into DNA

  20. Degradação de poliolefinas utilizando catalisadores zeolíticos Degradation of polyolefins using zeolitic catalysts

    Directory of Open Access Journals (Sweden)

    Maria Letícia M. Valle

    2004-03-01

    Full Text Available Neste trabalho foi estudada a degradação de alguns dos principais constituintes dos rejeitos plásticos (polietileno de alta densidade (HDPE, polietileno de baixa densidade (LDPE e polipropileno (PP, empregando-se um catalisador exausto de unidades de craqueamento de fluidos (FCC e um catalisador zeolítico (ADZ3 sintetizado em laboratório. Utilizando técnicas de termogravimetria (TG-DTG e cromatografia gasosa (CG, foi possível avaliar os produtos gerados no craqueamento destas poliolefinas. Na degradação catalítica de poliolefinas com catalisadores zeolíticos, verificou-se a obtenção preferencial de gasolina, GLP e diesel, produtos importantes na matriz energética brasileira. O catalisador de FCC exausto foi mais seletivo para a produção de gasolina e GLP, enquanto que a produção de diesel foi mais favorecida com o catalisador ADZ3.In this work the degradation of some of the main plastics responsible for waste, viz. high density polyethylene (HDPE, low density polyethylene (LDPE and polypropylene (PP, was studied using a spent FCC catalyst (fluid cracking catalyst and a zeolitic catalyst (ADZ3 synthesized in laboratory. Using thermogravimetry (TG-DTG and gas chromatography (GC techniques, it was possible to evaluate the products from these polyolefins cracking. The catalytic degradation of polyolefins led to a preferential production of LPG, diesel and gasoline, which are important products of the Brazilian energetic matrix. The spent FCC catalyst was more selective for production of LPG and gasoline, whereas the diesel production was more favored with the ADZ3 catalyst.

  1. Synthesis of novel conformationally locked carbocyclic nucleosides derived from 5,5- and 6,6-bis(hydroxymethyl)bicyclo[2.2.1]heptan-2-ol

    Czech Academy of Sciences Publication Activity Database

    Hřebabecký, Hubert; Masojídková, Milena; Holý, Antonín

    2005-01-01

    Roč. 70, č. 4 (2005), s. 519-538 ISSN 0010-0765 R&D Projects: GA ČR(CZ) GA203/05/0132 Institutional research plan: CEZ:AV0Z40550506 Keywords : azides * amines * cyclic sulfates Subject RIV: CC - Organic Chemistry Impact factor: 0.949, year: 2005

  2. CATALYZED CYCLIZATION OF [ALPHA],[OMEGA]-DIENES: A VERSATILE PROTOCOL FOR THE SYNTHESIS OF FUNCTIONALIZED CARBOCYCLIC AND HETEROCYCLIC COMPOUNDS. (R826120)

    Science.gov (United States)

    The perspectives, information and conclusions conveyed in research project abstracts, progress reports, final reports, journal abstracts and journal publications convey the viewpoints of the principal investigator and may not represent the views and policies of ORD and EPA. Concl...

  3. Stability of tramadol with three 5-HT3 receptor antagonists in polyolefin bags for patient-controlled delivery systems

    Directory of Open Access Journals (Sweden)

    Chen FC

    2016-06-01

    Full Text Available Fu-chao Chen,1 Jun Zhu,1 Bin Li,1 Fang-jun Yuan,1 Lin-hai Wang2 1Department of Pharmacy, Dongfeng Hospital, 2Department of Pharmacy, Renmin Hospital, Hubei University of Medicine, Shiyan, Hubei, People’s Republic of China Background: Mixing 5-hydroxytryptamine-3 (5-HT3 receptor antagonists with patient-controlled analgesia (PCA solutions of tramadol has been shown to decrease the incidence of nausea and vomiting associated with the use of tramadol PCA for postoperative pain. However, such mixtures are not commercially available, and the stability of the drug combinations has not been duly studied. The study aimed to evaluate the stability of tramadol with three 5-HT3 receptor antagonists in 0.9% sodium chloride injection for PCA administration.Materials and methods: Test samples were prepared by adding 1,000 mg tramadol hydrochloride, 8 mg ondansetron hydrochloride, and 6 mg granisetron hydrochloride or 5 mg tropisetron hydrochloride to 100 mL of 0.9% sodium chloride injection in polyolefin bags. The samples were prepared in triplicates, stored at either 25°C or 4°C for 14 days, and assessed using the following compatibility parameters: precipitation, cloudiness, discoloration, and pH. Chemical stability was also determined using a validated high-pressure liquid chromatography method.Results: All of the mixtures were clear and colorless throughout the initial observation period. No change in the concentration of tramadol hydrochloride occurred with any of the 5-HT3 receptor antagonists during the 14 days. Similarly, little or no loss of the 5-HT3 receptor antagonists occurred over the 14-day period.Conclusion: Our results suggest that mixtures of tramadol hydrochloride, ondansetron hydrochloride, granisetron hydrochloride, or tropisetron hydrochloride in 0.9% sodium chloride injection were physically and chemically stable for 14 days when stored in polyolefin bags at both 4°C and 25°C. Keywords: tramadol, ondansetron, granisetron

  4. Unimpeded permeation of water through biocidal graphene oxide sheets anchored on to 3D porous polyolefinic membranes

    Science.gov (United States)

    Mural, Prasanna Kumar S.; Jain, Shubham; Kumar, Sachin; Madras, Giridhar; Bose, Suryasarathi

    2016-04-01

    3D porous membranes were developed by etching one of the phases (here PEO, polyethylene oxide) from melt-mixed PE/PEO binary blends. Herein, we have systematically discussed the development of these membranes using X-ray micro-computed tomography. The 3D tomograms of the extruded strands and hot-pressed samples revealed a clear picture as to how the morphology develops and coarsens over a function of time during post-processing operations like compression molding. The coarsening of PE/PEO blends was traced using X-ray micro-computed tomography and scanning electron microscopy (SEM) of annealed blends at different times. It is now understood from X-ray micro-computed tomography that by the addition of a compatibilizer (here lightly maleated PE), a stable morphology can be visualized in 3D. In order to anchor biocidal graphene oxide sheets onto these 3D porous membranes, the PE membranes were chemically modified with acid/ethylene diamine treatment to anchor the GO sheets which were further confirmed by Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and surface Raman mapping. The transport properties through the membrane clearly reveal unimpeded permeation of water which suggests that anchoring GO on to the membranes does not clog the pores. Antibacterial studies through the direct contact of bacteria with GO anchored PE membranes resulted in 99% of bacterial inactivation. The possible bacterial inactivation through physical disruption of the bacterial cell wall and/or reactive oxygen species (ROS) is discussed herein. Thus this study opens new avenues in designing polyolefin based antibacterial 3D porous membranes for water purification.3D porous membranes were developed by etching one of the phases (here PEO, polyethylene oxide) from melt-mixed PE/PEO binary blends. Herein, we have systematically discussed the development of these membranes using X-ray micro-computed tomography. The 3D tomograms of the extruded strands and

  5. Physicochemical stability of ternary admixtures of butorphanol, ketamine, and droperidol in polyolefin bags for patient-controlled analgesia use

    Directory of Open Access Journals (Sweden)

    Fang BX

    2016-11-01

    Full Text Available Baoxia Fang,1 Linhai Wang,2 Junfeng Gu,3 Fuchao Chen,1 Xiao-ya Shi1 1Department of Pharmacy, Dongfeng Hospital, 2Department of Pharmacy, 3Department of Anesthesiology, Renmin Hospital, Hubei University of Medicine, Hubei, People’s Republic of China Background: Delivery of drug admixtures by intravenous patient-controlled analgesia is a common practice for the management of postoperative pain; however, analytical confirmation of the compatibility and stability of butorphanol tartrate, ketamine hydrochloride, and droperidol combined in ternary admixtures is not available.Methods: Butorphanol tartrate, ketamine hydrochloride, and droperidol have been examined for compatibility and stability when combined with 0.9% sodium chloride injection stored at 4°C and 25°C with light protection for a total of 14 days. Concentrations were 0.067 mg/mL, 1.33 mg/mL, and 0.033 mg/mL for butorphanol tartrate, ketamine hydrochloride, and droperidol, respectively. Drug concentrations were determined using high-performance liquid chromatographic analysis.Results: All three drugs were very stable (>97% at 4°C and 25°C for 14 days. The ternary admixtures were initially clear and colorless throughout the observation period, and the pH value did not change significantly.Conclusion: The results confirm that the ternary admixture of butorphanol tartrate 0.067 mg/mL, ketamine hydrochloride 1.33 mg/mL, and droperidol 0.033 mg/mL in 0.9% sodium chloride injection were stable for 14 days when stored in polyolefin bags at 4°C and 25°C and protected from light. Keywords: analgesia, patient-controlled analgesia, drug stability, butorphanol, ketamine, droperidol, HPLC

  6. Stability-indicating HPLC method for the determination of the stability of oxytocin parenteral solutions prepared in polyolefin bags.

    Science.gov (United States)

    Kaushal, G; Sayre, B E; Prettyman, T

    2012-02-01

    Oxytocin is very commonly used in clinical settings and is a nonapeptide hormone that stimulates the contraction of uterine smooth muscles. In this study the stability of extemporaneously compounded oxytocin solutions was investigated in polyolefin bags. The sterile preparations of oxytocin were compounded to the strength of 0.02 U/mL in accordance with United States Pharmacopeia (USP) standards. In order to carry out the stability testing of these parenteral products, the solutions were stored under three different temperature conditions of -20°C (frozen), 2-6°C (refrigerated), and 22-25°C (room temperature). Three solutions from each temperature were withdrawn and were assessed for stability on days 0, 7, 15, 21, and 30 as per the USP guidelines. The assay of oxytocin was examined by an HPLC method at each time point. No precipitation, cloudiness or color change was observed during this study at all temperatures. The assay content by HPLC revealed that oxytocin retains greater than at least 90% of the initial concentrations for 21 days. There was no significant change in pH and absorbance values for 21 days under all the conditions of storage. Oxytocin parenteral solutions in the final concentration of 0.02 U/mL and diluted in normal saline are stable for at least 30 days under frozen and refrigerated conditions for 30 days. At the room temperature, the oxytocin solutions were stable for at least 21 days. The stability analysis results show that the shelf-life of 21 days observed in this study was far better than their recommended expiration dates.

  7. The C8-2′-Deoxyguanosine Adduct of 2-Amino-3-methylimidazo[1,2-d]naphthalene, a Carbocyclic Analogue of the Potent Mutagen 2-Amino-3-methylimidazo[4,5-f]quinoline (IQ), is a Block to Replication in Vitro

    Science.gov (United States)

    Christov, Plamen P.; Chowdhury, Goutam; Garmendia, Craig A.; Wang, Feng; Stover, James S.; Elmquist, C. Eric; Kozekova, Albena; Angel, Karen C.; Turesky, Robert J.; Stone, Michael P.; Guengerich, F. Peter; Rizzo, Carmelo J.

    2010-01-01

    2-Amino-3-methylimidazo[4,5-f]naphthelene is a carbocyclic analogue of the dietary carcinogen 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) in which a naphthalene ring system replaces the quinoline unit of IQ. The activity of 2-amino-3-methylimidazo[4,5-f]naphthelene (cIQ) in Ames Salmonella typhimurium tester strain TA98 is known to be 4-5 orders of magnitude lower than IQ. 2-Amino-3-methylimidazo[4,5-f]naphthelene undergoes efficient bioactivation with rat liver microsomes. The C8-dGuo adduct was formed when calf thymus DNA was treated with the N-hydroxy-cIQ metabolite and either acetic anhydride or extracts from cells that overexpress N-acetyl transferase (NAT). These studies indicate that bioactivation, the stability of the N-hydroxylamine ester, and the reactivity of the nitrenium ion with DNA of cIQ are similar to IQ and that none of these factors account for the differences in mutagenic potency of these analogues in Ames assays. Oligonucleotides were synthesized that contain the C8-dGuo adduct of 2-amino-3-methylimidazo[4,5-f]naphthelene in the frameshift-prone CG-dinucleotide repeat unit of the NarI recognition sequence. We have examined the in vitro translesion synthesis of this adduct and find it to be a strong replication block to E. coli DNA polymerase I, Klenow fragment exo− (Kf−), E. coli DNA polymerase II exo− (pol II−), and Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4). Previous studies by Fuchs and coworkers identified E. coli pol II as the polymerase responsible for two-base deletions of the C8-dGuo adduct of N-acetyl-2-aminofluorene in the NarI sequence. Our observation that pol II is strongly inhibited by the C8-dGuo adduct of 2-amino-3-methylimidazo[4,5-f]naphthelene suggests that one of the other SOS inducible polymerases (E. coli pol IV or pol V) is required for its bypass and this accounts for the greatly attenuated mutagenicity in Ames assays compared with IQ. PMID:20377178

  8. Nanosized carbon black combined with Ni2O3 as "universal" catalysts for synergistically catalyzing carbonization of polyolefin wastes to synthesize carbon nanotubes and application for supercapacitors.

    Science.gov (United States)

    Wen, Xin; Chen, Xuecheng; Tian, Nana; Gong, Jiang; Liu, Jie; Rümmeli, Mark H; Chu, Paul K; Mijiwska, Ewa; Tang, Tao

    2014-04-01

    The catalytic carbonization of polyolefin materials to synthesize carbon nanotubes (CNTs) is a promising strategy for the processing and recycling of plastic wastes, but this approach is generally limited due to the selectivity of catalysts and the difficulties in separating the polyolefin mixture. In this study, the influence of nanosized carbon black (CB) and Ni2O3 as a novel combined catalyst system on catalyzing carbonization of polypropylene (PP), polyethylene (PE), polystyrene (PS) and their blends was investigated. We showed that this combination was efficient to promote the carbonization of these polymers to produce CNTs with high yields and of good quality. Catalytic pyrolysis and model carbonization experiments indicated that the carbonization mechanism was attributed to the synergistic effect of the combined catalysts rendered by CB and Ni2O3: CB catalyzed the degradation of PP, PE, and PS to selectively produce more aromatic compounds, which were subsequently dehydrogenated and reassembled into CNTs via the catalytic action of CB together with Ni particles. Moreover, the performance of the synthesized CNTs as the electrode of supercapacitor was investigated. The supercapacitor displayed a high specific capacitance as compared to supercapacitors using commercial CNTs and CB. This difference was attributed to the relatively larger specific surface areas of our synthetic CNTs and their more oxygen-containing groups.

  9. Room-Temperature High-Efficiency Solid-State Triplet-Triplet Annihilation Up-Conversion in Amorphous Poly(olefin sulfone)s.

    Science.gov (United States)

    Turshatov, Andrey; Busko, Dmitry; Kiseleva, Natalia; Grage, Stephan L; Howard, Ian A; Richards, Bryce S

    2017-03-08

    Triplet-triplet annihilation up-conversion (TTA-UC) is a developing technology that can enable spectral conversion under sunlight. Previously, it was found that efficient TTA-UC can be realized in polymer hosts for temperatures above the polymer's glass transition (T > T g ). In contrast, TTA-UC with high quantum yield for temperatures below T g is rarely reported. In this article, we report new polymer hosts in which efficient TTA-UC is observed well below T g , when the polymer is in a fully solid state. The four poly(olefin sulfone) hosts were loaded with upconversion dyes, and absolute quantum yields of TTA-UC (η TTA-UC ) were measured. The highest value of η TTA-UC = 2.1% was measured for poly(1-dodecene sulfone). Importantly, this value was the same in vacuum and at ambient conditions, indicating that the host material acts as a good oxygen barrier. We performed time-resolved luminescence experiments in order to elucidate the impact of elementary steps of TTA-UC. In addition to optical characterization, we used magic angle spinning solid-state NMR experiments to estimate the T2 transverse relaxation time. Relatively long T2 times measured for poly(olefin sulfone)s indicate an enhanced nanoscale fluidity in the studied (co)polymers, which unexpectedly coexists with a rigidity on the macroscale. This would explain the exceptional triplet energy transfer between the guest molecules, despite the macroscopic rigidity.

  10. Long-term stability of morphine hydrochloride in 0.9% NaCl infusion polyolefin bags after freeze-thaw treatment and in polypropylene syringes at 5 degrees C + 3 degrees C.

    Science.gov (United States)

    Hecq, J-D; Godet, M; Gillet, P; Jamart, J; Galanti, L

    2014-01-01

    The aim of this study was to investigate the long-term stability of morphine hydrochloride in 0.9% NaCI infusion polyolefin bags and polypropylene syringes after storage at 5 degrees C + 3 degrees C and to evaluate the influence of initial freezing and microwave thawing on this stability. Ten polyolefin bags and five polypropylene syringes containing 100 mL of 1 mg/mL of morphine hydrochloride solution in 0.9% NaCI were prepared under aseptic conditions. Five polyolefin bags were frozen at -20 degrees C for 90 days before storage. Immediately after the preparation and after thawing, 2 mL of each bag were withdrawn for the initial concentration measurements. All polyolefin bags and polypropylene syringes were then refrigerated at 5 degrees C + 3 degrees C for 58 days during which the morphine concentrations were measured periodically by high-performance liquid chromatography using a reversed-phase column, naloxone as internal standard, a mobile phase consisting of 5% acetonitrile and 95% of KH2PO4 buffer (pH 3.50), and detection with diode array detector at 254 nm. Visual and microscopic observations and spectrophotometric and pH measurements were also performed. Solutions were considered stable if the concentration remained superior to 90% of the initial concentration. The degradation products peaks were not quantitatively significant and were resolved from the native drug. Polyolefin bag and polypropylene syringe solutions were stable when stored at 5 degrees C + 3 degrees C during these 58 days. No color change or precipitation in the solutions was observed. The physical stability was confirmed by visual, microscopic, and spectrophotometric inspection. There was no significant change in pH during storage. Freezing and microwave thawing didn't influence the infusion stability. Morphine hydrochloride infusions may be prepared in advance by centralized intravenous additive service, frozen in polyolefin bags, and microwave thawed before storage under refrigeration

  11. Effect of freezing, long-term storage and microwave thawing on the stability of a mixture of diclofenac and sodium bicarbonate in glucose 5% polyolefin bags.

    Science.gov (United States)

    François, J-H; Hecq, J-D; Vanbeckbergen, D; Jamart, J; Galanti, L

    2009-11-01

    Preparation in advance of intravenous solution could be efficient to improve quality assurance, security, time management and cost saving of drug delivery. The aim of this study was to investigate the stability of a mixture of diclofenac 75 mg/100 ml and sodium bicarbonate 42 mg/100 ml in 5% glucose polyolefin bags after freezing, long-term storage, and microwave thawing. The stability of five polyolefin bags containing approximately 75 mg/100ml of diclofenac and 42 mg/100ml of sodium bicarbonate in 5% glucose prepared under aseptic conditions was studied after freezing for 2 months at -20 degrees C, thawing in a microwave oven with a validated cycle, and stored at 5 + or - 3 degrees C. Diclofenac concentrations were measured by high-pressure liquid chromatography using a reversed-phase column, a mobile phase consisting of 40% of acetonitrile (v/v) in KH(2)PO(4) buffer 0.02 M, pH 8.40 + or - 0.05, and UV detection at 276.0 nm. Visual inspection, microscope observation, spectrophotometric measurements and pH measurement were also performed. No colour change or precipitation occurred in the preparations. No microaggregate was observed with optical microscopy or revealed by a change of absorbance. Based on a shelf-life of 90% residual potency, diclofenac was stable for at least 30 days after freezing and microwave thawing, period where 95% lower confidence limit of the concentration-time profile remained superior to 90% of the initial concentration. During this period, the pH values of drug solutions have not been altered. Within these limits, diclofenac in 5% glucose infusion may be prepared and frozen in advance by a centralized intravenous admixture service, then thawed before use in clinical units.

  12. Thermodynamic analysis of mechanical behaviour in the elastic region of blends of recycled poly (ethylene terephthalate) and recycled polyolefins; Analise termodinamica do comportamento mecanico na regiao elastica de blendas de poli (tereftalato de etileno) reciclado e poliolefinas recicladas

    Energy Technology Data Exchange (ETDEWEB)

    Marconcini, Jose M. [Universidade Federal do Parana Univ. (UFPR), Curitiba, PR (Brazil). Inst. de Tecnologia para o Desenvolvimento; Ruvolo Filho, Adhemar [Universidade Federal de Sao Carlos (UFSCar), SP (Brazil). Dept. de Quimica]. E-mail: adhemar@power.ufscar.br

    2006-10-15

    This work describes the study using mechanical tests with the blend of recycled poly(ethylene terephthalate) (PET) and recycled polyolefin with and without the addition of polypropylene grafted with maleic anhydride and poly(ethylene-co-octene-1). A thermodynamic approach based on the Helmholtz work function was applied in the analysis of mechanical tests, correlating the effects of energy storage and from the compatibilizer on the elastic region of the materials. For the system studied, the polyolefin-rich region shows higher storage of elastic energy corroborating the morphology images obtained from SEM analysis. The thermodynamic analysis seems a useful tool to evaluate the compatibilizer effect in polymeric immiscible blends. In this work, more specifically, this method was used to analyze the mechanical behavior of different compositions of recycled polymeric commodity materials. (author)

  13. Controlled synthesis of stereoblock polypropylene. New trends in the development of elastomers

    International Nuclear Information System (INIS)

    Bravaya, Natal'a M; Nedorezova, Polina M; Tsvetkova, Valentina I

    2002-01-01

    The review generalises published data on the synthesis of elastomeric stereoblock polypropylene, a representative of thermoelastoplastics, which are prepared by random or block copolymerisation of various co-monomers and are widely used in the manufacture of diverse mechanical rubber goods. New unique applications of metallocene and post-metallocene catalysts in the design of polyolefin elastomers with a broad spectrum of physicomechanical characteristics are discussed. Particular attention is given to modern homogeneous catalyst systems based on Group IVB element metallocene complexes, which ensure highly efficient synthesis of polypropylene elastomers with various stereoblock structures. Data on the specific features of the structure and properties of the elastomeric stereoblock polypropylene are analysed. The bibliography includes 160 references.

  14. Long-term Stability of Esomeprazole in 5% Dextrose Infusion Polyolefin Bags at 5 degrees C +/- 3 degrees C after Microwave Freeze-thaw Treatment.

    Science.gov (United States)

    Hecq, Jean-daniel; Rolin, Catherine; Godet, Marie; Gillet, Patricia; Jamart, Jacques; Galanti, Laurence M

    2015-01-01

    To improve quality assurance, security, time management, and cost saving of drug delivery, preparation in advance of intravenous solutions has been developed for several infusion solutions. The objective of this study was to investigate the stability of esomeprazole 0.4 mg/mL and 0.8 mg/mL in 5% dextrose polyolefin bags after freezing, long-term storage, and microwave thawing. The stability of five polyolefin bags containing approximately 0.4 mg/mL of esomeprazole and five other bags containing approximately 0.8 mg/mL in 5% dextrose prepared under aseptic conditions was studied after freezing for 1 month at -20 degrees C, thawing in a microwave oven with a validated cycle, and stored at 5 degrees C +/- 3 degrees C. Esomeprazole concentration was measured by high-pressure liquid chromatography using a reversed-phase column C8, a mobile phase consisting of 35% of acetonitrile and 65% of Na2HPO4 buffer at pH 7.59 with HPO4 (2 M) and NaOH (0.5 M), and detection with a diode array detector at 280 nm. Visual, microscopic, and spectrophotometric observation and pH measurements were also performed. No precipitation occurred in the preparations but little change of color was observed. No microaggregate was observed with optical microscopy or revealed by a change of absorbance at 350, 410, and 550 nm. Based on a shelf life of 90% residual potency, esomeprazole solutions (0.4 and 0.8 mg/mL) were stable for at least 20 or 29 days, respectively, after a freezing and microwave thawing period, where 95% one-side lower confidence limit of the concentration-time profile remained superior to 90% of the initial concentration. During this period, the pH values of drug solutions have been observed to decrease without affecting chromatographic parameters. Within these limits, esomeprazole (0.4 and 0.8 mg/mL) in 5% dextrose infusions may be prepared and frozen in advance by a centralized intravenous admixture service, thawed, and stored at least 20 days at 5 degrees C +/- 3 degrees C

  15. Using synchrotron-based FT-IR microspectroscopy to study erucamide migration in 50-micron-thick bilayer linear low-density polyethylene and polyolefin plastomer films.

    Science.gov (United States)

    Sankhe, Shilpa Y; Hirt, Douglas E

    2003-01-01

    The diffusion of additives in thick (approximately 500 microns) single layer and multilayer films has been characterized using FT-IR microspectroscopy. The objective of this research was to investigate additive migration and concentration profiles in coextruded multilayer films of industrially relevant thicknesses. In particular, the investigation focused on the migration of an erucamide slip agent in 50-micron-thick coextruded bilayer films of linear low-density polyethylene (LLDPE) and a polyolefin plastomer (POP). Erucamide concentration profiles were successfully mapped using synchrotron-based FT-IR microspectroscopy. The synchrotron radiation helped to achieve a higher spatial resolution for the thin films. Meticulous sample preparation was needed to map the thin film samples. Results with FT-IR microspectroscopy showed that the additive-concentration profiles were relatively uniform across the multilayer-film thickness irrespective of the intended initial additive distribution. For example, a bilayer planned for 1 wt % erucamide in an LLDPE layer and no erucamide in a POP layer showed significant additive migration into the POP layer at the extrusion rates used. FT-IR microspectroscopy results also showed that more erucamide migrated to the surface of a POP layer than an LLDPE layer. Attenuated total reflectance (ATR) FT-IR spectroscopy was used to confirm the time-dependent increase of erucamide surface concentration and that the increase was more pronounced at the surface of the POP layers.

  16. 3,7-Dideazaneplanocin: Synthesis and antiviral analysis.

    Science.gov (United States)

    Yin, Xue-Qiang; Schneller, Stewart W

    2017-12-01

    Objective To synthesize 3,7-dideazaneplanocin and evaluate its antiviral potential. Methods The target 3,7-dideazaneplanocin has been prepared in five steps from a readily available cyclopentenol. A thorough in vitro antiviral analysis was conducted versus both DNA and RNA viruses. Results A rational synthesis of 3,7-dideazaneplanocin was conceived and successfully pursued in such a way that it can be adapted to various analogs of 3,7-dideazaneplanocin. Using standard antiviral assays, no activity for 3,7-dideazaneplanocn was found. Conclusion Two structural features are necessary for adenine-based carbocyclic nucleosides (like neplanocin) for potential antiviral properties: (i) inhibition of S-adenosylhomocysteine hydrolase and/or (ii) C-5' activation via the mono-nucleotide. These two requisite adenine structural features to fit these criteria are not present in in the target 3,7-dideazaneplanocin: (i) an N-7 is necessary for inhibition of the hydrolase and the N-3 is claimed to be essential for phosphorylation at C-5'. Thus, it is not surprising that 3,7-dideazaneplaoncin lacked antiviral properties.

  17. Development of a Unified Enantioselective, Convergent Synthetic Approach Toward the Furanobutenolide-Derived Polycyclic Norcembranoid Diterpenes: Asymmetric Formation of the Polycyclic Norditerpenoid Carbocyclic Core by Tandem Annulation Cascade.

    Science.gov (United States)

    Craig, Robert A; Smith, Russell C; Roizen, Jennifer L; Jones, Amanda C; Virgil, Scott C; Stoltz, Brian M

    2018-04-06

    An enantioselective and diastereoselective approach toward the synthesis of the tetracyclic scaffold of the furanobutenolide-derived polycyclic norditerpenoids is described. Focusing on synthetic efforts toward ineleganolide, the synthetic approach utilizes a palladium-catalyzed enantioselective allylic alkylation for the construction of the requisite chiral tertiary ether. A diastereoselective cyclopropanation-Cope rearrangement cascade enabled the convergent assembly of the ineleganolide [6,7,5,5]-tetracyclic scaffold. Investigation of substrates for this critical tandem annulation process is discussed along with synthetic manipulations of the [6,7,5,5]-tetracyclic scaffold and the attempted interconversion of the [6,7,5,5]-tetracyclic scaffold of ineleganolide to the isomeric [7,6,5,5]-core of scabrolide A and its naturally occurring isomers. Computational evaluation of ground-state energies of late-stage synthetic intermediates was used to guide synthetic development and aid in the investigation of the conformational rigidity of these highly constrained and compact polycyclic structures.

  18. Total synthesis of eudesmane terpenes by site-selective C-H oxidations.

    Science.gov (United States)

    Chen, Ke; Baran, Phil S

    2009-06-11

    From menthol to cholesterol to Taxol, terpenes are a ubiquitous group of molecules (over 55,000 members isolated so far) that have long provided humans with flavours, fragrances, hormones, medicines and even commercial products such as rubber. Although they possess a seemingly endless variety of architectural complexities, the biosynthesis of terpenes often occurs in a unified fashion as a 'two-phase' process. In the first phase (the cyclase phase), simple linear hydrocarbon phosphate building blocks are stitched together by means of 'prenyl coupling', followed by enzymatically controlled molecular cyclizations and rearrangements. In the second phase (the oxidase phase), oxidation of alkenes and carbon-hydrogen bonds results in a large array of structural diversity. Although organic chemists have made great progress in developing the logic needed for the cyclase phase of terpene synthesis, particularly in the area of polyene cyclizations, much remains to be learned if the oxidase phase is to be mimicked in the laboratory. Here we show how the logic of terpene biosynthesis has inspired the highly efficient and stereocontrolled syntheses of five oxidized members of the eudesmane family of terpenes in a modicum of steps by a series of simple carbocycle-forming reactions followed by multiple site-selective inter- and intramolecular carbon-hydrogen oxidations. This work establishes an intellectual framework in which to conceive the laboratory synthesis of other complex terpenes using a 'two-phase' approach.

  19. Produtos poliolefínicos reciclados com desempenho superior aos materiais virgens correspondentes Recycled polyolefin products with higher performance than the corresponding virgin materials

    Directory of Open Access Journals (Sweden)

    Agnes F. Martins

    1999-12-01

    Full Text Available O balanço das reações de reticulação e cisão em cadeias poliolefínicas, quando expostas a condições ambientais de radicais livres, pode resultar em boas propriedades e novas aplicações. Materiais descartados de alta qualidade despertam cada vez mais interesse para reciclagem. Os resíduos plásticos de embalagens alimentícias, assim como peças descartadas de grandes dimensões, provenientes da indústria automotiva, são exemplos daqueles materiais. No presente trabalho, são relatadas as propriedades mecânicas da madeira plástica IMAWOOD, obtida a partir de resíduos sólidos urbanos, principalmente embalagens de polietileno, e do material IMACAR, recuperado de pára-choques descartados de carros de passeio, constituído basicamente de misturas PP/EPDM. Verificou-se que o IMAWOOD mostrou comportamento mecânico melhorado por efeito da radiação-gama, enquanto que o IMACAR revelou alta resistência ao impacto, muito superior ao material virgem de composição correspondente.The balance of crosslinking and scission reactions in polyolefin chains when exposed to free-radical, environmental conditions may result in good properties and new applications. Discarded, post-consumer high quality materials are more and more attractive for recycling. The plastic residues from food packages and large dimension automobile residues, as car bumpers, are good examples of those materials. In the present work, we report mechanical properties of IMAWOOD®, plastic lumber from urban solid waste, mostly PE packaging residues, and IMACAR, from discarded car bumpers, mainly PP/EPDM blends. IMAWOOD® showed improved mechanical behavior after gamma-irradiation. IMACAR® was highly resistant to impact.

  20. Effect of freeze-thawing on the long-term stability of calcium levofolinate in 5% dextrose stored on polyolefin infusion bags.

    Science.gov (United States)

    Lebitasy, M; Hecq, J-D; Athanassopoulos, A; Vanbeckbergen, D; Jamart, J; Galanti, L

    2009-08-01

    Calcium levofolinate infusions could be prepared in advance by a centralized intravenous additive service (CIVAS) to improve safety and time management. To investigate the effect of freezing, microwave thawing and long-term storage at 5 +/- 3 degrees C on the stability of calcium levofolinate in 5% dextrose solution. Solutions of 250 mL of 5% dextrose in polyolefin bags (n = 5) containing approximately 400 mg of calcium levofolinate were prepared under aseptic conditions and frozen for 95 days at -20 degrees C. The solutions were then thawed using microwaves and stored at 5 +/- 3 degrees C for 1 month. The calcium levofolinate concentrations were measured by high performance liquid chromatography (HPLC). Visual inspection was performed and pH was measured periodically during the storage at 5 +/- 3 degrees C. Stability of the solution was defined as a concentration remaining superior to 90% of the initial concentration by regression analysis as recommended by the Food and Drug Administration (FDA). No colour change or precipitation in the solutions was observed. Calcium levofolinate infusions were stable when stored at 5 +/- 3 degrees C during 1 month after freeze-thaw treatment. Throughout this period, the lower confidence limit of the estimated regression line of concentration-time profile remained above 90% of the initial concentration. Slight change in pH values from 6.52 +/- 0.01 to 6.50 +/- 0.01 during storage time did not affect retention time on HPLC and has no clinical consequence, the solutions remaining in the acceptable range for perfusion (4

  1. Synthesis of racemic 9-(6- and 2,6-substituted 9H-purin-9-yl)-5-oxatricyclo[4.2.1.03,7]nonane-3-methanols, novel conformationally locked carbocyclic nucleosides

    Czech Academy of Sciences Publication Activity Database

    Hřebabecký, Hubert; Masojídková, Milena; Holý, Antonín

    2005-01-01

    Roč. 70, č. 1 (2005), s. 103-123 ISSN 0010-0765 Institutional research plan: CEZ:AV0Z40550506 Keywords : amines * oximes * nucleosides Subject RIV: CC - Organic Chemistry Impact factor: 0.949, year: 2005

  2. Contribuições recentes da reação de hidroformilação na síntese de produtos farmacêuticos: parte II Current improvement to the synthesis of pharmaceuticals by hydrofor-mylation reaction: part II

    Directory of Open Access Journals (Sweden)

    Carlo Botteghi

    1997-02-01

    Full Text Available The hydroformylation reaction represents one of the most important C1-chemistry area in the chemical industry. This catalytic process, which has been developed up to now mainly to the production of commodities chemicals, has shown a remarkable potential for the preparation of several categories of specialty chemicals and in particular pharmaceutical compounds. Arylpropanoic acids, various amines containing aryl groups, and intermediates for the preparation of vitamins, carbocyclic and heterocyclic compounds and many other classes of organic molecules endowed with pharmacological activity are currently accessible in good-to-high yields through hydroformylation of selected olefinic substrates. The asymmetric hydroformylation is going to reach the stage of maturity and hence to contribute in solving many troublesome synthetic problems connected with the preparation of pharmacologically active compounds with very high enantiomeric purity. The present survey emphasizes the usefulness of synthesis gas as a starting material in fine chemistry, which is expected to be important for industry.

  3. Thermal Oxidation of Polyolefins by Mild Pro-Oxidant Additives Based on Iron Carboxylates and Lipophilic Amines: Degradability in the Absence of Light and Effect on the Adhesion to Paperboard

    Directory of Open Access Journals (Sweden)

    Tuan-Anh Nguyen

    2015-08-01

    Full Text Available Marine and inland pollution by non-degradable plastic bags and other plastic articles is a topic of great concern. Natural degradation processes based on oxidation of plastic pollutants could possibly contribute to limit the extent of pollution. Thermal degradation of polyolefins in the absence of light by non-polluting pro-oxidants has not been presented before. In this study, we show that two amines, stearyl amine and [(3-(11-aminoundecanoyl amino propane-1-] silsesquioxane (amino-POSS in combination with ferric stearate (FeSt3 tremendously accelerate the thermal oxidation of polyolefins compared with reference samples. Both amines and FeSt3 are to a large extent based on renewable resources. Polyethylene and polypropylene samples containing less than 100 ppm of iron and 1% of amine were extremely brittle after 10 days in a circulation oven in the absence of light. No significant degradation could be seen with samples containing iron but no amine. In a different application, the initial oxidation of polyethylene can be used in order to increase its adhesion to cardboard. Excellent adhesion between polyethylene and cardboard is important for liquid packaging based on renewable resources. Amino-POSS has been chosen for food packaging applications due to its expected lower leakage from polyethylene (PE compared with stearyl amine. Film samples of PE/amino-POSS/FeSt3 blends were partly oxidized in a circulation oven. The oxidation was documented by increased carbonyl index (CI and melt flow index (MFI. The limited extent of oxidation has been proved by unchanged tensile strength and only moderate changes in elongation at break when compared to reference polyethylene films containing no FeSt3 or amino-POSS. The PE/amino-POSS/FeSt3 blends were compression moulded to paperboard. The adhesion of non-aged blends to paperboard decreased with increasing amino-POSS content which is in good compliance with an earlier reported lubricant effect of high

  4. Carbocyclic Carbohydrate Mimics as Potential Glycosidase Inhibitors

    DEFF Research Database (Denmark)

    Fanefjord, Mette; Lundt, Inge

    It has been proven that aminocyclopentanols having the aminogroup adjacent to a carbon sidechain could be potential anomer-selective glycosidase inhibitors [1]. A successful pathway for synthesising mimics to L-carbohydrates 2, by introducing nitrogen to the C6 position in compound 1, has been...... developed in our group. A similar strategy has been used for synthesising mimics of D-carbohydrates. The α,β-unsaturated lactone 3 was cyclised to compound 4 which was further transformed into 5. The nitrogen functionality in compound 7 is introduced by an Overman rearrangement of 6 and the hydroxyl...

  5. Long-term stability of temocillin in dextrose 5% and in sodium chloride 0.9% polyolefin bags at 5 ± 3°C after freeze-thaw treatment.

    Science.gov (United States)

    Rolin, C; Hecq, J-D; Tulkens, P; Vanbeckbergen, D; Jamart, J; Galanti, L

    2011-11-01

    The aim of this study was to investigate the stability of a mixture of temocillin 20mg/ml in 5% dextrose and in 0.9% sodium chloride polyolefin bags after freezing, microwave thawing and long-term storage at 5±3°C. The stability of ten polyolefin bags containing 20mg/ml of temocillin, five bags in 5% dextrose and five bags in 0.9% sodium chloride, prepared under aseptic conditions was studied after freezing for 1 month at -20°C, thawing in a microwave oven with a validated cycle, and stored at 5±3°C. Over 30 days, temocillin concentrations were measured by high-pressure liquid chromatography. Visual inspections, microscope observation, spectrophotometric measurements and pH measurements were also performed. No precipitation occurred in the preparations but minor colour change was observed. No microaggregate was observed with optical microscopy or revealed by a change of absorbance. Based on a shelf life of 95% residual potency, temocillin infusions were stable at least 11 days in 5% dextrose and 14 days in 0.9% sodium chloride after freezing and microwave thawing (corresponding at the period where 95% lower confidence limit of the concentration-time profile remained superior to 95% of the initial concentration). During this period, the pH values of drug solutions have been observed to decrease without affecting chromatographic parameters. Within these limits, temocillin in 5% dextrose and in 0.9% sodium chloride infusions may be prepared and frozen in advance by a centralized intravenous admixture service then thawed before use in clinical units. Copyright © 2011 Elsevier Masson SAS. All rights reserved.

  6. Polyolefin nanocomposites in situ polymerization

    International Nuclear Information System (INIS)

    Galland, Griselda Barrera; Fim, Fabiana de C.; Milani, Marceo A.; Silva, Silene P. da; Forest, Tadeu; Radaelli, Gislaine; Basso, Nara R.S.; Quijada, Raul

    2011-01-01

    Polyethylene and polypropylene nanocomposites using grapheme nanosheets and treated chrysotile have been synthesized by in situ polymerization using metallocene catalysts. The fillers have been submitted to acid, thermal and/ou ultrasound treatments before to introduce them into the polymerization reactor. A complete characterization of the fillers has been done. The nanocomposites have been characterized by SEM, TEM, DRX and AFM. The thermal, mechanic -dynamic, mechanical and electrical properties of the nanocomposites are discussed. (author)

  7. Radiation-stable polyolefin compositions

    International Nuclear Information System (INIS)

    Rekers, J.W.

    1986-01-01

    This invention relates to compositions of olefinic polymers suitable for high energy radiation treatment. In particular, the invention relates to olefinic polymer compositions that are stable to sterilizing dosages of high energy radiation such as a gamma radiation. Stabilizers are described that include benzhydrol and benzhydrol derivatives; these stabilizers may be used alone or in combination with secondary antioxidants or synergists

  8. Organic synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Thomas, S.E.

    1991-01-01

    This paper reports on reactions of organoboranes. Organoboron routes to unsaturated hydrocarbons. Boronic ester homologation. Properties of organosilicon compounds. Alkene synthesis (Peterson olefination). Allylsilanes and acylsilanes.

  9. Fire Synthesis

    Indian Academy of Sciences (India)

    1000ºC or special infrastructure which require careful maintenance. In such a situation fire synthesis is a simpler method that can be adopted for the bulk production of high purity alumina and related oxides. Fire Synthesis. Preparation of Alumina ...

  10. Organic synthesis

    International Nuclear Information System (INIS)

    Lallemand, J.Y.; Fetizon, M.

    1988-01-01

    The 1988 progress report of the Organic Synthesis Chemistry laboratory (Polytechnic School, France), is presented. The laboratory activities are centered on the chemistry of natural products, which have a biological activity and on the development of new reactions, useful in the organic synthesis. The research works involve the following domains: the natural products chemistry which are applied in pharmacology, the plants and insects chemistry, the organic synthesis, the radical chemistry new reactions and the bio-organic physicochemistry. The published papers, the congress communications and the thesis are listed [fr

  11. Fire Synthesis

    Indian Academy of Sciences (India)

    her PhD degree from. Bangalore University. She is currently working as a Research Associate at the Department of. Inorganic and Physical. Chemistry, Indian. Institute of Science,. Bangalore, on the synthesis of .... This method uses the experiences of propellant chemistry in making the redox mixture. The . stoichiometry or ...

  12. Fire Synthesis

    Indian Academy of Sciences (India)

    special infrastructure which require careful maintenance. In such situation fire synthesis is a simpler method that can be adopted for the bulk production of high purity .... reaction between Ti and B to form titanium boride. The reaction between titanium (fuel- electron donor) and boron (oxidiser-electron acceptor) once initiated ...

  13. Fire Synthesis

    Indian Academy of Sciences (India)

    Home; Journals; Resonance – Journal of Science Education; Volume 16; Issue 12. Fire Synthesis - Preparation of Alumina Products. Tanu Mimani. Volume 16 Issue 12 December 2011 pp 1324-1332. Fulltext. Click here to view fulltext PDF. Permanent link: http://www.ias.ac.in/article/fulltext/reso/016/12/1324-1332 ...

  14. Fire Synthesis

    Indian Academy of Sciences (India)

    Home; Journals; Resonance – Journal of Science Education; Volume 5; Issue 2. Fire Synthesis - Preparation of Alumina Products. Tanu Mimani. General Article Volume 5 Issue 2 February 2000 pp 50-57. Fulltext. Click here to view fulltext PDF. Permanent link: http://www.ias.ac.in/article/fulltext/reso/005/02/0050-0057 ...

  15. Influence of clay type on the performance of Ziegler-Natta catalyst for the synthesis of nanocomposites of PE and PP; Influencia do tipo de argila no desempenho de catalisadores Ziegler-Natta para a sintese de nanocompositos de PE e PP

    Energy Technology Data Exchange (ETDEWEB)

    Almeida, Lidiane A.; Marques, Maria F.V., E-mail: fmarques@ima.ufrj.br [Instituto de Macromoleculas Professora Eloisa Mano (UFRJ), Centro de Tecnologia, RJ (Brazil); Oliveira, Jaqueline S. [Escola de Quimica - (EQ/UFRJ), Centro de Tecnologia, Rio de Janeiro, RJ (Brazil)

    2011-07-01

    Polymer nanocomposites present highly improved general properties in comparison with original polymer and their conventional composites. The mayor disadvantage in preparing these materials is the difficulty in the dispersion of the nanofillers in the polymer matrix. In the present work, the synthesis of bisupported (MgCl{sub 2}/clay) catalyst was performed for obtaining polyethylene and polypropylene nanocomposites by in situ polymerization with the aim to achieve higher dispersion of the nanofillers in the polyolefin matrix. Moreover, the influence of ammonium salt (employed in the organophilization of the clay) on the fixation of the catalyst components and therefore, on the catalyst activity was evaluated. The catalysts were characterized by TGA, SEM, EDX, and XRD. Polymers were characterized by DSC, isotactic index through heptane extractables (HS), TGA, EDX, XRD, and optical microscopy (OM). The results showed that the type of clay modifier has a great influence on the catalyst performance. (author)

  16. Long-term stability of acyclovir in 0.9% NaCl infusion polyolefin bags at 5±3°C after freeze-thaw treatment: a generic product versus the brand name.

    Science.gov (United States)

    Dewulf, J; Galanti, L; Godet, M; Gillet, P; Jamart, J; Hecq, J-D

    2015-03-01

    The aim of the study was to investigate the long-term stability of acyclovir 5 mg/mL (a generic product versus the brand name) in NaCl 0.9% after storage at 5±3°C and to evaluate the influence of initial freezing and microwave thawing on this stability. Five bags of Acyclovir® Hospira 5 mg/mL (A) and five bags of Zovirax® GSK 5 mg/mL (B) were prepared under aseptic conditions and stored 3 months at -20°C, then thawed and stored 30 days at 4°C. Five bags of Acyclovir® 5 mg/mL (C) and five bags of Zovirax® 5 mg/mL (D) were also prepared under aseptic conditions and stored 30 days at 5±3°C. Optic density measurement at different wavelengths, pH measurement and optic microscope observations were performed periodically during the storage. A forced degradation test with HCl 12 M and NaOH 5 M before and after heating at 100°C was also performed. The concentrations were measured by HPLC-PDA. The only one forced degradation test that yielded chromatograms with degradation products peak was the test with the acid solution heated at 100°C without interference with the native product. No significant change in pH values or optic densities were seen during the study for both products. No crystals were seen with the optic microscope during the study. Acyclovir® and Zovirax® solutions were stable for at least 21 days according to the FDA recommendations. Moreover, there was no statistical difference between regression lines of those two products and two storage conditions. Under the conditions of this study, Acyclovir® 5 mg/mL in 100 mL of NaCl 0.9% infusion remains stable at least for 21 days at 5±3°C with or without freezing at -20°C during the three previous months. There is no statistical difference between the brand name and a generic product. Acyclovir may be prepared in advanced by a centralized intravenous additive service, frozen in polyolefin bags and microwave thawed before storage under refrigeration until 21 days. Copyright © 2014 Elsevier Masson

  17. Crack propagation in a welded polyolefin pipe

    Czech Academy of Sciences Publication Activity Database

    Ševčík, Martin; Hutař, Pavel; Náhlík, Luboš; Lach, R.; Knésl, Zdeněk; Grellmann, W.

    2012-01-01

    Roč. 3, č. 2 (2012), s. 148 ISSN 1757-9864 R&D Projects: GA ČR GC101/09/J027 Institutional support: RVO:68081723 Keywords : polymers * pipes * butt weld * crack Subject RIV: JL - Materials Fatigue, Friction Mechanics

  18. Multifunctional Polyolefin Matrix Composite Structures, Phase II

    Data.gov (United States)

    National Aeronautics and Space Administration — Polyethylene, and ultrahigh molecular weight polyethylene (UHMWPE) in particular, is an outstanding material for radiation shielding in the sense that its...

  19. Halogen-free flame retardant polyolefin foams

    OpenAIRE

    Redondo Realinho, Vera Cristina de; Antunes, Marcelo de Sousa Pais; Santana Pérez, Orlando Onofre; Velasco Perero, José Ignacio

    2012-01-01

    The present work deals with the preparation and characterizacion of an improved fire-resistant ethylene-acrylate foamed material containing calcium carbonate and a silicon elastomer. This grade, usually employed on the cable industry sector, was modified two differents synergistic FR systems : silica/zinc borate (S/ZB) and montmorillonite/graphite nanoplatelets(N). The different formulations were prepared by melt-blending and the foams by a compression-molding foaming process using Azodicarbo...

  20. Magnetic Density Separation of Polyolefin Wastes

    NARCIS (Netherlands)

    Hu, B.

    2014-01-01

    Polymer recycling has significantly positive impacts on the environment, economics and society. Using recycled polymer to replace virgins reduces the growing amount of post-consumer polymer wastes, decreases the demand for fossil fuel and creates local jobs. As the most used polymer types,

  1. Total synthesis of ciguatoxin.

    Science.gov (United States)

    Hamajima, Akinari; Isobe, Minoru

    2009-01-01

    Something fishy: Ciguatoxin (see structure) is one of the principal toxins involved in ciguatera poisoning and the target of a total synthesis involving the coupling of three segments. The key transformations in this synthesis feature acetylene-dicobalthexacarbonyl complexation.

  2. Microwave-promoted synthesis of bicyclic azocine-β-lactams from bis(allenes).

    Science.gov (United States)

    Alcaide, Benito; Almendros, Pedro; Aragoncillo, Cristina; Fernández, Israel; Gómez-Campillos, Gonzalo

    2014-08-01

    A metal-free preparation of structurally novel bicyclic azocine-β-lactams has been developed. The first examples accounting for the preparation of eight-membered rings from bis(allenes) in the absence of metals have been achieved by the thermolysis of nonconjugated 2-azetidinone-tethered bis(allenes) on application of microwave irradiation. This selective carbocyclization reaction has been studied experimentally, and additionally, its mechanism has been investigated by a DFT study.

  3. Análise termodinâmica do comportamento mecânico na região elástica de blendas de poli (tereftalato de etileno reciclado e poliolefinas recicladas Thermodynamic analysis of mechanical behaviour in the elastic region of blends of recycled poly (ethylene terephthalate and recycled polyolefins

    Directory of Open Access Journals (Sweden)

    José M. Marconcini

    2006-12-01

    Full Text Available Este trabalho descreve o estudo de blendas de poli(tereftalato de etileno reciclado e poliolefinas recicladas, com e sem adição de polipropileno funcionalizado com anidrido maleico e poli(etileno-co-octeno-1 utilizando ensaios mecânicos e microscopia eletrônica de varredura. Foi aplicado um formalismo termodinâmico com base na função trabalho de Helmholtz para o comportamento mecânico na região elástica, correlacionando-se com o armazenamento de energia elástica para os materiais estudados. Também foi analisada a dissipação de energia relativa ao fenômeno elasto-plástico na região de baixas deformações. Para as blendas estudadas, observou-se que o armazenamento de energia e o efeito do compatibilizante são muito mais acentuados na região rica em poliolefinas, corroborando com as imagens da morfologia observadas via microscopia eletrônica. A análise termodinâmica apresentada mostrou-se uma ferramenta útil e confiável e de baixo custo, para avaliar o efeito de compatibilização de sistemas poliméricos imiscíveis. No presente trabalho, particularmente para a avaliação do comportamento mecânico de misturas de materiais "commodities" reciclados.This work describes the study using mechanical tests with the blend of recycled poly(ethylene terephthalate (PET and recycled polyolefin with and without the addition of polypropylene grafted with maleic anhydride and poly(ethylene-co-octene-1. A thermodynamic approach based on the Helmholtz work function was applied in the analysis of mechanical tests, correlating the effects of energy storage and from the compatibilizer on the elastic region of the materials. For the system studied, the polyolefin-rich region shows higher storage of elastic energy corroborating the morphology images obtained from SEM analysis. The thermodynamic analysis seems a useful tool to evaluate the compatibilizer effect in polymeric immiscible blends. In this work, more specifically, this method was

  4. Synthesis of Mechanisms

    DEFF Research Database (Denmark)

    Hansen, John Michael

    1999-01-01

    These notes describe an automated procedure for analysis and synthesis of mechanisms. The analysis method is based on the body coordinate formulation, and the synthesis is based on applying optimization methods, used to minimize the difference between an actual and a desired behaviour......These notes describe an automated procedure for analysis and synthesis of mechanisms. The analysis method is based on the body coordinate formulation, and the synthesis is based on applying optimization methods, used to minimize the difference between an actual and a desired behaviour...

  5. Total Synthesis of Avrainvilleol.

    Science.gov (United States)

    Wegener, Aaron; Miller, Kenneth A

    2017-11-03

    The first total synthesis of the marine natural product avrainvilleol is reported. The total synthesis features the first application of the transition-metal-free coupling of a tosyl hydrazone and a boronic acid to the preparation of a complex natural product, and the first example of this coupling with a hindered diortho substituted hydrazone substrate.

  6. Difluoromethylenephosphonates: synthesis and transformations

    International Nuclear Information System (INIS)

    Chunikhin, Konstantin S; Kadyrov, A A; Pasternak, P V; Chkanikov, Nikolai D

    2010-01-01

    The data on the synthesis of organic compounds containing the difluoromethylenephosphonate group are analyzed and generalized. The attention is focused on the introduction of this group into various organic molecules and subsequent transformations of the compounds thus formed. Individual sections are devoted to the synthesis of heterocyclic compounds and analogues of natural substances containing difluoromethylenephosphonate groups.

  7. Synthesis of Isoiminosugars

    DEFF Research Database (Denmark)

    Hyldtoft, Lene; Godskesen, Michael Anders; Lundt, Inge

    1998-01-01

    A short synthesis of isoiminosugars have been developed. Bromolactones are diastereoselectively alkylated at C-2 followed by ring closure to the corresponding lactams. Reduction of these then gives isoiminosugars......A short synthesis of isoiminosugars have been developed. Bromolactones are diastereoselectively alkylated at C-2 followed by ring closure to the corresponding lactams. Reduction of these then gives isoiminosugars...

  8. Synthesis of oligonucleotide phosphorodithioates

    DEFF Research Database (Denmark)

    Beaton, G.; Brill, W. K D; Grandas, A.

    1991-01-01

    The synthesis of DNA containing sulfur at the two nonbonding internucleotide valencies is reported. Several different routes using either tervalent or pentavalent mononucleotide synthons are described.......The synthesis of DNA containing sulfur at the two nonbonding internucleotide valencies is reported. Several different routes using either tervalent or pentavalent mononucleotide synthons are described....

  9. VHDL for logic synthesis

    CERN Document Server

    Rushton, Andrew

    2011-01-01

    Many engineers encountering VHDL (very high speed integrated circuits hardware description language) for the first time can feel overwhelmed by it. This book bridges the gap between the VHDL language and the hardware that results from logic synthesis with clear organisation, progressing from the basics of combinational logic, types, and operators; through special structures such as tristate buses, register banks and memories, to advanced themes such as developing your own packages, writing test benches and using the full range of synthesis types. This third edition has been substantially rewritten to include the new VHDL-2008 features that enable synthesis of fixed-point and floating-point hardware. Extensively updated throughout to reflect modern logic synthesis usage, it also contains a complete case study to demonstrate the updated features. Features to this edition include: * a common VHDL subset which will work across a range of different synthesis systems, targeting a very wide range of technologies...

  10. Lewis base additives improve the zeolite ferrierite-catalyzed synthesis of isostearic acid

    Science.gov (United States)

    Isostearic acid (IA) is of interest for industrial purposes especially in the area of biolubricants, such as cosmetics and slip additives for polyolefin and related copolymer films. This study was designed to develop a zeolitic catalysis process for IA production through isomerization of fatty aci...

  11. Asymmetric synthesis v.4

    CERN Document Server

    Morrison, James

    1984-01-01

    Asymmetric Synthesis, Volume 4: The Chiral Carbon Pool and Chiral Sulfur, Nitrogen, Phosphorus, and Silicon Centers describes the practical methods of obtaining chiral fragments. Divided into five chapters, this book specifically examines initial chiral transmission and extension. The opening chapter describes the so-called chiral carbon pool, the readily available chiral carbon fragments used as building blocks in synthesis. This chapter also provides a list of 375 chiral building blocks, along with their commercial sources, approximate prices, and methods of synthesis. Schemes involving

  12. SYNTHESIS, CHARACTERIZATION AND ANTIBACTERIAL ...

    African Journals Online (AJOL)

    Preferred Customer

    E-mail: a-ahmadi@kiau.ac.ir; ahmadikiau@yahoo.com. SYNTHESIS, CHARACTERIZATION AND ANTIBACTERIAL EVALUATION OF. SOME NOVEL DERIVATIVES OF 2-BROMOMETHYL-BENZIMIDAZOLE. Abbas Ahmadi*. Department of Medicinal Chemistry, Pharmaceutical Sciences Branch, Islamic Azad University,.

  13. 2002 Annual report: synthesis

    International Nuclear Information System (INIS)

    2003-01-01

    This synthesis of the Annual Report 2002 presents information of the main activities on the scope of the radiation protection and nuclear safety of the Nuclear Regulatory Authority (ARN) of the Argentina during 2002

  14. 2001 Annual report: synthesis

    International Nuclear Information System (INIS)

    2001-01-01

    This synthesis of the Annual Report 2001 presents information of the main activities on the scope of the radiation protection and nuclear safety of the Nuclear Regulatory Authority (ARN) of the Argentina during 2001

  15. 2000 Annual report: synthesis

    International Nuclear Information System (INIS)

    2001-01-01

    This synthesis of the Annual Report 2000 present information of the main activities on the scope of the radiation protection and nuclear safety of the Nuclear Regulatory Authority (NRA) of the Argentina during 2000

  16. Synthesis of Acetylhomoagmatine

    Directory of Open Access Journals (Sweden)

    Carmenza Duque

    2006-08-01

    Full Text Available Abstract: The first total synthesis of acetylhomoagmatine, a natural product isolated form the methanolic extracts from the sponge Cliona celata, is performed in four steps in a very high yield.

  17. Instrument Modeling and Synthesis

    Science.gov (United States)

    Horner, Andrew B.; Beauchamp, James W.

    During the 1970s and 1980s, before synthesizers based on direct sampling of musical sounds became popular, replicating musical instruments using frequency modulation (FM) or wavetable synthesis was one of the “holy grails” of music synthesis. Synthesizers such as the Yamaha DX7 allowed users great flexibility in mixing and matching sounds, but were notoriously difficult to coerce into producing sounds like those of a given instrument. Instrument design wizards practiced the mysteries of FM instrument design.

  18. Detonation-synthesis nanodiamonds: synthesis, structure, properties and applications

    International Nuclear Information System (INIS)

    Dolmatov, Valerii Yu

    2007-01-01

    The review outlines the theoretical foundations and industrial implementations of modern detonation synthesis of nanodiamonds and chemical purification of the nanodiamonds thus obtained. The structure, key properties and promising fields of application of detonation-synthesis nanodiamonds are considered.

  19. Synthesis of phenanthrenes

    International Nuclear Information System (INIS)

    Clarke, C.

    1983-01-01

    A new and improved synthesis of 7-methoxy-12-methyl-2-oxo-2,3,4,9,10,12-hexahydrophenanthrene has been described. The compound is an important intermediate for the synthesis of many di- and tri-terpenes, and was required in this work for the synthesis of 17-acetyl-5α-etiojerva-12,14,16-trien-3β-ol. This compound is a known starting material for the synthesis of the veratrum alkaloids jervine, veratramine and verarine. Two synthetic routes to the synthesis of 7-methoxy-12-methyl-2-oxo-2,3,4,9,10,12-hexahydrophenanthrene were investigated. The first route required preparation of the intermediate 1-(5-methyl-2-furyl)-3-(3'-methoxyphenyl)propane which, by simple manipulation involving mainly the furan ring, gave the desired compound in 33% yield. All of the reactions involved are suitable for both large and small scale preparations. The synthesis of 17-acetyl-5α-etiojerva-12,14,16-trien-3B-ol can be achieved by the hyde and 3-methoxyacetophenone, followed by hydrogeneration and Wolff-Kishner reduction. A less successful synthesis of the above compound was achieved by condensing the Grignard derivative of 2-(3'-methoxyphenyl)ethyl bromide with 5-methylfurfuraldehyde to form a furyl alcohol, which was oxidized and reduced to give 1-(5-methyl-2-furyl)-3-(3'-methoxyphenyl)propane in only 7% overall yield, but the starting materials are inexpensive and readily available. The compound was also prepared in 40% yield by condensing 2-lithio-5-methylfuran with 3-(3'methoxyphenyl)propyl bromide. An appendix describes the reaction of 3-ethoxy-cyclohex-2-en-1-one with ethylmagnesium bromide, followed by aromatization. A second appendix describes the reductive alkylation of 8-methoxy-12-methyl-2-oxo-2,3,4,9,10,12-hexahydrophenanthrene

  20. Ionic Liquids in Electro-active Devices (ILED)

    Science.gov (United States)

    2013-12-12

    of Physical Chemistry B, (03 2010): . doi: B. aitken, M. Lee, M. Hunley, H. Gibson, K. Wagener . Synthesis of Precision Ionic Polyolefins Derived...2008): . doi: B. Aitken, M. Lee, M. Hunley, H. Gibson, K. Wagener . Synthesis of precision ionic polyolefins derived from ionic liquids...Harry W. Gibson, Karen I. Winey, Brian S. Aitken, Kenneth B. Wagener . Precision Ionomers: Synthesis and Thermal/Mechanical Characterization

  1. Behavioral synthesis of asynchronous circuits

    DEFF Research Database (Denmark)

    Nielsen, Sune Fallgaard

    2005-01-01

    This thesis presents a method for behavioral synthesis of asynchronous circuits, which aims at providing a synthesis flow which uses and tranfers methods from synchronous circuits to asynchronous circuits. We move the synchronous behavioral synthesis abstraction into the asynchronous handshake...... is idle. This reduces unnecessary switching activity in the individual functional units and therefore the energy consumption of the entire circuit. A collection of behavioral synthesis algorithms have been developed allowing the designer to perform time and power constrained design space exploration...

  2. Synthesis of organosilicon compounds

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, G. [Iowa State Univ., Ames, IA (United States)

    1996-01-01

    Silicon-containing polymers have been a focus of synthesis and study in Dr. Barton`s group because of their chemistry and properties which are not offered by other systems or materials. For example, the polymer -[-SiMe2C≡C-]n-can be easily processed to films or fibers from melt or solution, and thermally converted to a SiC-containing ceramic in high yield at high temperature. In recent years, carbosilane dendritic polymers have been of great interests in many research groups. However, no synthesis of carbosilane dendrimers with functionalties both inside and outside the dendrimer has been reported. Functionality is very important in the synthesis of preceramic polymers. This thesis will be devoted to exploring several new organosilicon polymer systems.

  3. Total Synthesis of Strychnine.

    Science.gov (United States)

    Lee, Geun Seok; Namkoong, Gil; Park, Jisook; Chen, David Y-K

    2017-11-16

    The total synthesis of the flagship Strychnos indole alkaloid, strychnine, has been accomplished. The developed synthetic sequence features a novel vinylogous 1,4-addition, a challenging iodinium salt mediated silyl enol ether arylation, a palladium-catalyzed Heck reaction, and a streamlined late-stage conversion to strychnine. Furthermore, an application of asymmetric counterion-directed catalysis (ACDC) in the context of target-oriented organic synthesis has been rendered access to an optically active material. The synthetic sequence described herein represents the most concise entry to optically active strychnine to date. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  4. Supercritical Synthesis of Biodiesel

    Directory of Open Access Journals (Sweden)

    Michel Vaultier

    2012-07-01

    Full Text Available The synthesis of biodiesel fuel from lipids (vegetable oils and animal fats has gained in importance as a possible source of renewable non-fossil energy in an attempt to reduce our dependence on petroleum-based fuels. The catalytic processes commonly used for the production of biodiesel fuel present a series of limitations and drawbacks, among them the high energy consumption required for complex purification operations and undesirable side reactions. Supercritical fluid (SCF technologies offer an interesting alternative to conventional processes for preparing biodiesel. This review highlights the advances, advantages, drawbacks and new tendencies involved in the use of supercritical fluids (SCFs for biodiesel synthesis.

  5. Direct dimethyl ether synthesis from synthesis gas: The influence of methanol dehydration on methanol synthesis reaction

    OpenAIRE

    Dadgar, Farbod; Myrstad, Rune; Pfeifer, Peter; Holmen, Anders; Venvik, Hilde Johnsen

    2016-01-01

    Direct dimethyl ether (DME) synthesis from synthesis gas is studied with regard to potential effects of methanol dehydration on methanol formation and copper-based catalyst performance. For this, the influence of the operating conditions (space velocity, temperature, pressure, time-on-stream and syngas composition) on activity, selectivity and stability of the catalyst was studied and compared for methanol synthesis and direct DME synthesis. The advantage of the direct over the two-step DME s...

  6. An Approach to Interface Synthesis

    DEFF Research Database (Denmark)

    Madsen, Jan; Hald, Bjarne

    1995-01-01

    Presents a novel interface synthesis approach based on a one-sided interface description. Whereas most other approaches consider interface synthesis as optimizing a channel to existing client/server modules, we consider the interface synthesis as part of the client/server module synthesis (which...... may contain the re-use of existing modules). The interface synthesis approach describes the basic transformations needed to transform the server interface description into an interface description on the client side of the communication medium. The synthesis approach is illustrated through a point......-to-point communication, but is applicable to synthesis of a multiple client/server environment. The interface description is based on a formalization of communication events....

  7. Enzymatic synthesis of vanillin

    NARCIS (Netherlands)

    van den Heuvel, RHH; Fraaije, MW; Laane, C; van Berkel, WJH; Heuvel, Robert H.H. van den; Berkel, Willem J.H. van

    Due to increasing interest in natural vanillin, two enzymatic routes for the synthesis of vanillin were developed. The flavoprotein vanillyl alcohol oxidase (VAO) acts on a wide range of phenolic compounds and converts both creosol and vanillylamine to vanillin with high yield. The VAO-mediated

  8. Enzymatic synthesis of vanillin

    NARCIS (Netherlands)

    Heuvel, van den R.H.H.; Fraaije, M.W.; Laane, C.; Berkel, van W.J.H.

    2001-01-01

    Due to increasing interest in natural vanillin, two enzymatic routes for the synthesis of vanillin were developed. The flavoprotein vanillyl alcohol oxidase (VAO) acts on a wide range of phenolic compounds and converts both creosol and vanillylamine to vanillin with high yield. The VAO-mediated

  9. Design synthesis exercise 2012

    NARCIS (Netherlands)

    Melkert, J.A.

    2013-01-01

    The design synthesis exercise forms the closing piece of the third year of the Bachelor degree curriculum of the Faculty of Aerospace Engineering at TU Delft. In this exercise the students learn to apply their acquired knowledge from all aerospace disciplines in one complete design. The object of

  10. Asymmetric synthesis of acetomycin

    NARCIS (Netherlands)

    Kinderman, S.S.; Feringa, B.L.

    1998-01-01

    The synthesis of (-)-acetomycin, a highly functionalized γ-lactone with antitumor activity, was achieved in five steps with nearly complete enantioselectivity. The key step was realized by a large scale lipase R catalyzed esterification of 5-hydroxy-4-methyl-2(5H)-furanone providing

  11. Synthesis de 1-dotriacotanol

    International Nuclear Information System (INIS)

    Hernandez, L.; Gonzalez, J.C.

    1996-01-01

    In order to prepare isotopic labeled long chain aliphatic primary alcohol's, the synthesis overall yielding and chemical purity of 1-dotriacotanol were 41% and 98%, respectively. This procedure is very useful for carbon-14 and tritium labeling at Beta position of saturated fatty alcohol's

  12. Synthesis of Camalexin

    Directory of Open Access Journals (Sweden)

    V. Kovacik

    2001-08-01

    Full Text Available In this paper we describe a new method for the synthesis of camalexin (1 based on the reaction of 1-(tert-butoxycarbonylindole-3-carboxaldehyde with methyl Lcysteinate hydrochloride, followed by oxidation and decarboxylation. Compounds 1, and intermediates 5-7 were identified by elemental analysis, 1H NMR, 13C NMR and mass spectroscopy.

  13. Synthesis of Camalexin

    OpenAIRE

    Dzurilla, M.; Kutschy, P.; Zaletova, J.; Ruzinsky, M.; Kovacik, V.

    2001-01-01

    In this paper we describe a new method for the synthesis of camalexin (1) based on the reaction of 1-(tert-butoxycarbonyl)indole-3-carboxaldehyde with methyl Lcysteinate hydrochloride, followed by oxidation and decarboxylation. Compounds 1, and intermediates 5-7 were identified by elemental analysis, 1H NMR, 13C NMR and mass spectroscopy.

  14. Synthesis of acrylic prepolymer

    International Nuclear Information System (INIS)

    Hussin bin Mohd Nor; Dahlan bin Haji Mohd; Mohamad Hilmi bin Mahmood.

    1988-04-01

    An acrylic prepolymer was synthesized from glycidyl methacrylate (GMA), butyl methacrylate (BMA), methyl methacrylate (MMA) and acrylic acid (AA). Butyl acetate (BAc), benzoyl peroxide (BzO), 4-methoxyphenol (MPh) and triethylamine (TEA) were used as solvent, initiator, inhibitor and catalyst respectively. Observations of the synthesis leading to the formation of acrylic prepolymer are described. (author)

  15. Synthesis, characterization and properties

    Indian Academy of Sciences (India)

    Unknown

    C−H⋅⋅⋅O bonds leading to an intricate hydrogen bonding network. Keywords. Synthesis .... in the refinement riding on their respective parent atoms. ..... nent peaks at 326 and 255 nm which can be assigned to transitions of the intramolecularly hydrogen-bon- ded salicylidenimino chromophore. Cotton effects of negative ...

  16. Synthesis of new radiotracers

    International Nuclear Information System (INIS)

    Chahed, Ahlem

    2008-01-01

    The brain's sensibility besides to the rigorous selectivity of changes taking place on brain's barriers leads us to synthesis specifics radiotracers based on diamine ethylene and marked with technetium radioisotope to form a radiotracer able to pass these barriers and diagnose illnesses in an early stage. These radiotracers are tested by a biodistribution on a small animal to be ratified. (Author)

  17. Synthesis of arabinoxylan fragments

    DEFF Research Database (Denmark)

    Underlin, Emilie Nørmølle; Böhm, Maximilian F.; Madsen, Robert

    , or production of commercial chemicals which are mainly obtained from fossil fuels today.The arbinoxylan fragments have a backbone of β-1,4-linked xylans with α-L-arabinose units attached at specific positions. The synthesis ultilises an efficient synthetic route, where all the xylan units can be derived from D...

  18. Total synthesis of aquatolide

    NARCIS (Netherlands)

    Saya, J.M.; Vos, K.; Klein Nijenhuis, R.A.; van Maarseveen, J.H.; Ingemann, S.; Hiemstra, H.

    2015-01-01

    A total synthesis of the sesquiterpene lactone aquatolide has been accomplished. The central step is an intramolecular [2 + 2]-photocycloaddition of an allene onto an alpha,beta-unsaturated delta-lactone. Other key steps are an intramolecular Horner-Wadsworth-Emmons reaction to close the lactone and

  19. The synthesis of gemcitabine.

    Science.gov (United States)

    Brown, Kylie; Dixey, Michael; Weymouth-Wilson, Alex; Linclau, Bruno

    2014-03-31

    Gemcitabine is a fluorinated nucleoside currently administered against a number of cancers. It consists of a cytosine base and a 2-deoxy-2,2-difluororibose sugar. The synthetic challenges associated with the introduction of the fluorine atoms, as well as with nucleobase introduction of 2,2-difluorinated sugars, combined with the requirement to have an efficient process suitable for large scale synthesis, have spurred significant activity towards the synthesis of gemcitabine exploring a wide variety of synthetic approaches. In addition, many methods have been developed for selective crystallisation of diastereomeric (including anomeric) mixtures. In that regard, the 2-deoxy-2,2-difluororibose sugar is one of the most investigated fluorinated carbohydrates in terms of its synthesis. The versatility of synthetic methods employed is illustrative of the current state of the art of fluorination methodology for the synthesis of CF2-containing carbohydrates, and involves the use of fluorinated building blocks, as well as nucleophilic and electrophilic fluorination of sugar precursors. Copyright © 2014. Published by Elsevier Ltd.

  20. Synthesis of the catalyst

    Indian Academy of Sciences (India)

    Admin

    62 11; Palhagen S, Canger R, Henriksen O, Van Parys J A, Riviere M E and Karolchyk M A 2001 Rufinamide: a double-blind, placebo-controlled proof of principle trial in patients with epilepsy; Epilepsy Res. 43, 115; Bakunov S A, Bakunova S M, Wenzler T, Ghebru M, Werbovetz K A, Brun R and Tidwell R R 2010 Synthesis ...

  1. Industrial scale gene synthesis.

    Science.gov (United States)

    Notka, Frank; Liss, Michael; Wagner, Ralf

    2011-01-01

    The most recent developments in the area of deep DNA sequencing and downstream quantitative and functional analysis are rapidly adding a new dimension to understanding biochemical pathways and metabolic interdependencies. These increasing insights pave the way to designing new strategies that address public needs, including environmental applications and therapeutic inventions, or novel cell factories for sustainable and reconcilable energy or chemicals sources. Adding yet another level is building upon nonnaturally occurring networks and pathways. Recent developments in synthetic biology have created economic and reliable options for designing and synthesizing genes, operons, and eventually complete genomes. Meanwhile, high-throughput design and synthesis of extremely comprehensive DNA sequences have evolved into an enabling technology already indispensable in various life science sectors today. Here, we describe the industrial perspective of modern gene synthesis and its relationship with synthetic biology. Gene synthesis contributed significantly to the emergence of synthetic biology by not only providing the genetic material in high quality and quantity but also enabling its assembly, according to engineering design principles, in a standardized format. Synthetic biology on the other hand, added the need for assembling complex circuits and large complexes, thus fostering the development of appropriate methods and expanding the scope of applications. Synthetic biology has also stimulated interdisciplinary collaboration as well as integration of the broader public by addressing socioeconomic, philosophical, ethical, political, and legal opportunities and concerns. The demand-driven technological achievements of gene synthesis and the implemented processes are exemplified by an industrial setting of large-scale gene synthesis, describing production from order to delivery. Copyright © 2011 Elsevier Inc. All rights reserved.

  2. Voice synthesis application

    Science.gov (United States)

    Lightstone, P. C.; Davidson, W. M.

    1982-04-01

    The military detection assessment laboratory houses an experimental field system which assesses different alarm indicators such as fence disturbance sensors, MILES cables, and microwave Racons. A speech synthesis board which could be interfaced, by means of a computer, to an alarm logger making verbal acknowledgement of alarms possible was purchased. Different products and different types of voice synthesis were analyzed before a linear predictive code device produced by Telesensory Speech Systems of Palo Alto, California was chosen. This device is called the Speech 1000 Board and has a dedicated 8085 processor. A multiplexer card was designed and the Sp 1000 interfaced through the card into a TMS 990/100M Texas Instrument microcomputer. It was also necessary to design the software with the capability of recognizing and flagging an alarm on any 1 of 32 possible lines. The experimental field system was then packaged with a dc power supply, LED indicators, speakers, and switches, and deployed in the field performing reliably.

  3. Synthesis of quantum dots

    Science.gov (United States)

    McDaniel, Hunter

    2017-10-17

    Common approaches to synthesizing alloyed quantum dots employ high-cost, air-sensitive phosphine complexes as the selenium precursor. Disclosed quantum dot synthesis embodiments avoid these hazardous and air-sensitive selenium precursors. Certain embodiments utilize a combination comprising a thiol and an amine that together reduce and complex the elemental selenium to form a highly reactive selenium precursor at room temperature. The same combination of thiol and amine acts as the reaction solvent, stabilizing ligand, and sulfur source in the synthesis of quantum dot cores. A non-injection approach may also be used. The optical properties of the quantum dots synthesized by this new approach can be finely tuned for a variety of applications by controlling size and/or composition of size and composition. Further, using the same approach, a shell can be grown around a quantum dot core that improves stability, luminescence efficiency, and may reduce toxicity.

  4. Prebiotic synthesis of histidine

    Science.gov (United States)

    Shen, C.; Yang, L.; Miller, S. L.; Oro, J.

    1990-01-01

    The prebiotic formation of histidine (His) has been accomplished experimentally by the reaction of erythrose with formamidine followed by a Strecker synthesis. In the first step of this reaction sequence, the formation of imidazole-4-acetaldehyde took place by the condensation of erythrose and formamidine, two compounds that are known to be formed under prebiotic conditions. In a second step, the imidazole-4-acetaldehyde was converted to His, without isolation of the reaction products by adding HCN and ammonia to the reaction mixture. LC, HPLC, thermospray liquid chromatography-mass spectrometry, and tandem mass spectrometry were used to identify the product, which was obtained in a yield of 3.5% based on the ratio of His/erythrose. This is a new chemical synthesis of one of the basic amino acids which had not been synthesized prebiotically until now.

  5. Distributed PROMPT-LTL Synthesis

    Directory of Open Access Journals (Sweden)

    Swen Jacobs

    2016-09-01

    Full Text Available We consider the synthesis of distributed implementations for specifications in Prompt Linear Temporal Logic (PROMPT-LTL, which extends LTL by temporal operators equipped with parameters that bound their scope. For single process synthesis it is well-established that such parametric extensions do not increase worst-case complexities. For synchronous systems, we show that, despite being more powerful, the distributed realizability problem for PROMPT-LTL is not harder than its LTL counterpart. For asynchronous systems we have to consider an assume-guarantee synthesis problem, as we have to express scheduling assumptions. As asynchronous distributed synthesis is already undecidable for LTL, we give a semi-decision procedure for the PROMPT-LTL assume-guarantee synthesis problem based on bounded synthesis.

  6. Microwave multicomponent synthesis.

    Science.gov (United States)

    Hügel, Helmut M

    2009-12-01

    In the manner that very important research is often performed by multidisciplinary research teams, the applications of multicomponent reactions involving the combination of multiple starting materials with different functional groups leading to the higher efficiency and environmentally friendly construction of multifunctional/complex target molecules is growing in importance. This review will explore the advances and advantages in microwave multicomponent synthesis (MMS) that have been achieved over the last five years.

  7. Microwave Multicomponent Synthesis

    Directory of Open Access Journals (Sweden)

    Helmut M. Hügel

    2009-12-01

    Full Text Available In the manner that very important research is often performed by multidisciplinary research teams, the applications of multicomponent reactions involving the combination of multiple starting materials with different functional groups leading to the higher efficiency and environmentally friendly construction of multifunctional/complex target molecules is growing in importance. This review will explore the advances and advantages in microwave multicomponent synthesis (MMS that have been achieved over the last five years.

  8. Microwave Multicomponent Synthesis

    OpenAIRE

    Helmut M. Hügel

    2009-01-01

    In the manner that very important research is often performed by multidisciplinary research teams, the applications of multicomponent reactions involving the combination of multiple starting materials with different functional groups leading to the higher efficiency and environmentally friendly construction of multifunctional/complex target molecules is growing in importance. This review will explore the advances and advantages in microwave multicomponent synthesis (MMS) that have been achiev...

  9. Synthesis of functionalised sulfonamides

    OpenAIRE

    Mok, B. L.

    2008-01-01

    Sulfonamides are important therapeutic agents and have a diverse array of biological functions in biology and medicine. Their means of synthesis has often involved the use of unstable sulfonyl chloride species; however, recent research has established pentafluorophenyl (PFP) sulfonate esters as a useful stable alternative to such species. This thesis describes the use of PFP vinyl sulfonate in a [3+2] cycloaddition with a variety of N-methyl-nitrones, providing access to the corresponding...

  10. Phase contrast image synthesis

    DEFF Research Database (Denmark)

    Glückstad, J.

    1996-01-01

    A new method is presented for synthesizing arbitrary intensity patterns based on phase contrast imaging. The concept is grounded on an extension of the Zernike phase contrast method into the domain of full range [0; 2 pi] phase modulation. By controlling the average value of the input phase funct...... function and by choosing appropriate phase retardation at the phase contrast filter, a pure phase to intensity imaging is accomplished. The method presented is also directly applicable in dark field image synthesis....

  11. Integrated methanol synthesis

    International Nuclear Information System (INIS)

    Jaeger, W.

    1982-01-01

    This invention concerns a plant for methanol manufacture from gasified coal, particularly using nuclear power. In order to reduce the cost of the hydrogen circuits, the methanol synthesis is integrated in the coal gasification plant. The coal used is gasified with hydration by means of hydrogen and the crude gas emerging, after cooling and separating the carbon dioxide and hydrogen sulphide, is mixed with the synthetic gas leaving the methane cracking furnace. This mixture is taken to the methanol synthesis and more than 90% is converted into methanol in one pass. The gas mixture remaning after condensation and separation of methanol is decomposed into three fractions in low temperature gas decomposition with a high proportion of unconverted carbon monoxide. The flow of methane is taken to the cracking furnace with steam, the flow of hydrogen is taken to the hydrating coal gasifier, and the flow of carbon monoxide is taken to the methanol synthesis. The heat required for cracking the methane can either be provided by a nuclear reactor or by the coke left after hydrating gasification. (orig./RB) [de

  12. Gold Nanoparticle Microwave Synthesis

    International Nuclear Information System (INIS)

    Krantz, Kelsie E.; Christian, Jonathan H.; Coopersmith, Kaitlin; Washington II, Aaron L.; Murph, Simona H.

    2016-01-01

    At the nanometer scale, numerous compounds display different properties than those found in bulk material that can prove useful in areas such as medicinal chemistry. Gold nanoparticles, for example, display promise in newly developed hyperthermia therapies for cancer treatment. Currently, gold nanoparticle synthesis is performed via the hot injection technique which has large variability in final particle size and a longer reaction time. One underdeveloped area by which these particles could be produced is through microwave synthesis. To initiate heating, microwaves agitate polar molecules creating a vibration that gives off the heat energy needed. Previous studies have used microwaves for gold nanoparticle synthesis; however, polar solvents were used that partially absorbed incident microwaves, leading to partial thermal heating of the sample rather than taking full advantage of the microwave to solely heat the gold nanoparticle precursors in a non-polar solution. Through this project, microwaves were utilized as the sole heat source, and non-polar solvents were used to explore the effects of microwave heating only as pertains to the precursor material. Our findings show that the use of non-polar solvents allows for more rapid heating as compared to polar solvents, and a reduction in reaction time from 10 minutes to 1 minute; this maximizes the efficiency of the reaction, and allows for reproducibility in the size/shape of the fabricated nanoparticles.

  13. Gold Nanoparticle Microwave Synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Krantz, Kelsie E. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Christian, Jonathan H. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Coopersmith, Kaitlin [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Washington, II, Aaron L. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Murph, Simona H. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2016-07-27

    At the nanometer scale, numerous compounds display different properties than those found in bulk material that can prove useful in areas such as medicinal chemistry. Gold nanoparticles, for example, display promise in newly developed hyperthermia therapies for cancer treatment. Currently, gold nanoparticle synthesis is performed via the hot injection technique which has large variability in final particle size and a longer reaction time. One underdeveloped area by which these particles could be produced is through microwave synthesis. To initiate heating, microwaves agitate polar molecules creating a vibration that gives off the heat energy needed. Previous studies have used microwaves for gold nanoparticle synthesis; however, polar solvents were used that partially absorbed incident microwaves, leading to partial thermal heating of the sample rather than taking full advantage of the microwave to solely heat the gold nanoparticle precursors in a non-polar solution. Through this project, microwaves were utilized as the sole heat source, and non-polar solvents were used to explore the effects of microwave heating only as pertains to the precursor material. Our findings show that the use of non-polar solvents allows for more rapid heating as compared to polar solvents, and a reduction in reaction time from 10 minutes to 1 minute; this maximizes the efficiency of the reaction, and allows for reproducibility in the size/shape of the fabricated nanoparticles.

  14. Application of chalcones in heterocycles synthesis: Synthesis of 2 ...

    Indian Academy of Sciences (India)

    Home; Journals; Journal of Chemical Sciences; Volume 125; Issue 3. Application of chalcones in heterocycles synthesis: Synthesis of 2-(isoxazolo, pyrazolo and pyrimido) substituted analogues of 1,4-benzodiazepin-5-carboxamides linked through an oxyphenyl bridge. N Kaur D Kishore. Volume 125 Issue 3 May 2013 pp ...

  15. Gene Synthesis with HG Khorana

    Indian Academy of Sciences (India)

    Home; Journals; Resonance – Journal of Science Education; Volume 17; Issue 12. Gene Synthesis with H G Khorana. Marvin H Caruthers. General Article Volume 17 Issue 12 December 2012 pp ... Keywords. Chemical synthesis of genes for yeast alanine tRNA and E. coli supressor tRNA; Khorana's philosophy on science.

  16. Organic synthesis with stable isotopes

    International Nuclear Information System (INIS)

    Blazer, R.M.; Daub, G.H.; Kerr, V.N.; Williams, D.L.; Whaley, T.W.

    1982-01-01

    Described is a scheme for the synthesis of L-arginine-1- 13 C utilizing methods developed for the synthesis of L-ornithine-1- 13 C from L-ornithine-2- 13 C and then converting ornithine into arginine with the enzyme acylase

  17. Chemical synthesis on SU-8

    DEFF Research Database (Denmark)

    Qvortrup, Katrine; Taveras, Kennedy; Thastrup, Ole

    2011-01-01

    In this paper we describe a highly effective surface modification of SU-8 microparticles, the attachment of appropriate linkers for solid-supported synthesis, and the successful chemical modification of these particles via controlled multi-step organic synthesis leading to molecules attached...

  18. Organic Synthesis using Clay Catalysts

    Indian Academy of Sciences (India)

    His work includes organic synthesis and reaction mechanisms mainly in the area of organosilicon chemistry. Presently he is also working on organic synthesis under solvent- free conditions and using clay-catalyses. Keywords. Montmorillonite, ion-exchange, clay-nanomaterials, dehydration pyrolysis, rearrangement, steric.

  19. First total synthesis of Boehmenan

    Indian Academy of Sciences (India)

    The first total synthesis of dilignan Boehmenan has been achieved. A biomimetic oxidative coupling of the ferulic acid methyl ester in the presence of silver oxide is the crucial step in the synthesis sequence, generating the dihydrobenzofuran skeleton. Hydroxyl group was protected with DHP and reducted with LiAlH4 to ...

  20. SHORT COMMUNICATION SYNTHESIS AND ANTIBACTERIAL ...

    African Journals Online (AJOL)

    Admin

    a. sodium nitrite, b. ethylacetoacetate, c. phenyl hydrazine, d. hydrazine hydrate, e. hydroxyl- amine hydrochloride, f. Salycylaldehye, g. chloroacetyl chloride, h. thioglycollic acid. Scheme 1. Synthesis of heterocyclic derivatives of sulfanilamide. Synthesis of compound 1 and 2a-e were done as per the reported method [7-8] ...

  1. Total synthesis of proposed auranthine.

    Science.gov (United States)

    Kshirsagar, Umesh A; Puranik, Vedavati G; Argade, Narshinha P

    2010-04-16

    Starting from CBz-protected glutamic anhydride and Boc-protected o-aminobenzyl amine, the first total synthesis of proposed structure of auranthine has been reported. An intramolecular aza-Wittig reaction involving a lactam carbonyl group that delivered the diazepine core unit was the key step in the synthesis.

  2. First total synthesis of Boehmenan

    Indian Academy of Sciences (India)

    Home; Journals; Journal of Chemical Sciences; Volume 126; Issue 3 ... The first total synthesis of dilignan Boehmenan has been achieved. A biomimetic oxidative coupling of the ferulic acid methyl ester in the presence of silver oxide is the crucial step in the synthesis sequence, generating the dihydrobenzofuran skeleton.

  3. Stereoselective total synthesis of sphingolipids

    Indian Academy of Sciences (India)

    Home; Journals; Journal of Chemical Sciences; Volume 128; Issue 11. Stereoselective total synthesis of sphingolipids. PARAMESH JANGILI PERLA ... Keywords. 1,2-Diacetyl D-erythro-sphinganine; 1,2-diacetyl L-threo-sphinganine; D-erythro-sphinganine triacetate; sphingolipids; total synthesis; Garner aldehyde.

  4. Chemical Synthesis of Antimicrobial Peptides.

    Science.gov (United States)

    Münzker, Lena; Oddo, Alberto; Hansen, Paul R

    2017-01-01

    Solid-phase peptide synthesis (SPPS) is the method of choice for chemical synthesis of peptides. In this nonspecialist review, we describe commonly used resins, linkers, protecting groups, and coupling reagents in 9-fluorenylmethyloxycarbonyl (Fmoc) SPPS. Finally, a detailed protocol for manual Fmoc SPPS is presented.

  5. Methyltrioctylammonium chloride catalysed sonochemical synthesis ...

    Indian Academy of Sciences (India)

    Home; Journals; Journal of Chemical Sciences; Volume 125; Issue 5. Methyltrioctylammonium chloride catalysed sonochemical synthesis of acridine diones ... The greener, clean and efficient protocol for the synthesis of acridine diones derivatives has been achieved by reacting aromatic aldehyde, dimedone and amines ...

  6. Lactobacillusassisted synthesis of titanium nanoparticles

    Directory of Open Access Journals (Sweden)

    Jha Anal

    2007-01-01

    Full Text Available AbstractAn eco-friendlylactobacillussp. (microbe assisted synthesis of titanium nanoparticles is reported. The synthesis is performed at room temperature. X-ray and transmission electron microscopy analyses are performed to ascertain the formation of Ti nanoparticles. Individual nanoparticles as well as a number of aggregates almost spherical in shape having a size of 40–60 nm are found.

  7. Microemulsion Synthesis of Nanoparticles

    Directory of Open Access Journals (Sweden)

    Gotić, M.

    2013-11-01

    Full Text Available Nanoparticles and nanomaterials have wide applications in electronics, physics, material design, being also utilized as sensors, catalysts, and more and more in biomedicine. Microemulsions are an exceptionally suitable medium for the synthesis of nanoparticles due to their thermodynamical stability, great solubility of both polar and nonpolar components, as well as their ability to control the size, dispersity and shape of the particles. This review presents microemulsion techniques for the synthesis of inorganic nanoparticles. It takes place in water-in-oil microemulsions by mixing one microemulsion with a cationic precursor, and the other with a precipitating or reducing agent, or by direct addition of reducing agents or gas (O2, NH3 ili CO2 into microemul sion (Fig. 1. Metal nanoparticles are used as catalysts, sensors, ferrofluids etc. They are produced by reducing the metal cation with a suitable reducing agent. In a similar way, one can prepare nanoparticles of alloys from the metal salts, provided that the metals are mutually soluble. The microemulsion technique is also suitable for depositing nanoparticles onto various surfaces. Highly active catalysts made from nanoparticles of Pt, Pd, Rh and other noble metals may be obtained in this way. Metal oxides and hydroxides may be prepared by hydrolysis or precipitation in the water core of microemulsion. Precipitation can be initiated by adding the base or precipitating agent into the microemulsion with water solution of metal ions. Similarly, nanoparticles may be prepared of sulphides, halogenides, cyanides, carbonates, sulphates and other insoluble metal salts. To prevent oxidation of nanoparticles, especially Fe, the particles are coated with inert metals, oxides, various polymers etc. Coating may provide additional functionality; e.g. coating with gold allows subsequent functionalization with organic compounds containing sulphur, due to the strong Au–S bond. Polymer coatings decrease

  8. Total Synthesis of Hyperforin.

    Science.gov (United States)

    Ting, Chi P; Maimone, Thomas J

    2015-08-26

    A 10-step total synthesis of the polycyclic polyprenylated acylphloroglucinol (PPAP) natural product hyperforin from 2-methylcyclopent-2-en-1-one is reported. This route was enabled by a diketene annulation reaction and an oxidative ring expansion strategy designed to complement the presumed biosynthesis of this complex meroterpene. The described work enables the preparation of a highly substituted bicyclo[3.3.1]nonane-1,3,5-trione motif in only six steps and thus serves as a platform for the construction of easily synthesized, highly diverse PPAPs modifiable at every position.

  9. Dibutylphosphoric acid synthesis

    International Nuclear Information System (INIS)

    Elias, H.; Boumaout, R.; Kellou, N.; Amedjkouh, A.; Hamidi, A.

    1995-09-01

    This work consists on the synthesis of dibutylphosphoric acis (DBP) by reaction of butanol with phosphorus pentoxid and on its separation by liquid-liquid extraction. It also deals with the characterization of DBP by some physicochemical analysis methods such as : chromatography, pH-metry and infrared and ultraviolet spectrophotometries. this study showed essentialy, that DBP can be formed in an appreciable amount (55%) when the reaction is realised with butanol/pentoxid molar ratio upper than 3 at temperature of 95 C

  10. Catalytic Oligopeptide Synthesis.

    Science.gov (United States)

    Liu, Zijian; Noda, Hidetoshi; Shibasaki, Masakatsu; Kumagai, Naoya

    2018-02-02

    Waste-free catalytic assembly of α-amino acids is fueled by a multiboron catalyst that features a characteristic B 3 NO 2 heterocycle, providing a versatile catalytic protocol wherein functionalized natural α-amino acid units are accommodated and commonly used protecting groups are tolerated. The facile dehydrative conditions eliminate the use of engineered peptide coupling reagents, exemplifying a greener catalytic alternative for peptide coupling. The catalysis is sufficiently robust to enable pentapeptide synthesis, constructing all four amide bond linkages in a catalytic fashion.

  11. Learning via Query Synthesis

    KAUST Repository

    Alabdulmohsin, Ibrahim Mansour

    2017-05-07

    Active learning is a subfield of machine learning that has been successfully used in many applications. One of the main branches of active learning is query synthe- sis, where the learning agent constructs artificial queries from scratch in order to reveal sensitive information about the underlying decision boundary. It has found applications in areas, such as adversarial reverse engineering, automated science, and computational chemistry. Nevertheless, the existing literature on membership query synthesis has, generally, focused on finite concept classes or toy problems, with a limited extension to real-world applications. In this thesis, I develop two spectral algorithms for learning halfspaces via query synthesis. The first algorithm is a maximum-determinant convex optimization method while the second algorithm is a Markovian method that relies on Khachiyan’s classical update formulas for solving linear programs. The general theme of these methods is to construct an ellipsoidal approximation of the version space and to synthesize queries, afterward, via spectral decomposition. Moreover, I also describe how these algorithms can be extended to other settings as well, such as pool-based active learning. Having demonstrated that halfspaces can be learned quite efficiently via query synthesis, the second part of this thesis proposes strategies for mitigating the risk of reverse engineering in adversarial environments. One approach that can be used to render query synthesis algorithms ineffective is to implement a randomized response. In this thesis, I propose a semidefinite program (SDP) for learning a distribution of classifiers, subject to the constraint that any individual classifier picked at random from this distributions provides reliable predictions with a high probability. This algorithm is, then, justified both theoretically and empirically. A second approach is to use a non-parametric classification method, such as similarity-based classification. In this

  12. Synthesis of deuterated clenbuterol

    Energy Technology Data Exchange (ETDEWEB)

    Joergensen, Ole [Risoe National Lab., Roskilde (Denmark). Solid State Physics Dept.; Egsgaard, Helge; Larsen, Elfinn [Risoe National Lab., Roskilde (Denmark). Science and Technology Dept.

    1996-11-01

    The synthesis of D{sub 9}-clenbuterol (I) and D{sub 3}-clenbuterol (II) is described. D{sub 9}-clenbuterol (I) was prepared from 4-amino-{alpha}-bromo-3, 5-dichloroacetophenone by reaction with D{sub 9}-tert-butylamine followed by reduction of the keto group with NaBH{sub 4}. D{sub 3}-clenbuterol (II) was prepared from 4-amino-{alpha}-tert-butylamino-3, 5-dichloroacetophenone by an exchange reaction of the {alpha}-hydrogens with deuterium followed by reduction of the keto group with NaBD{sub 4}. The eventual products were characterized by mass spectrometry and NMR. (author).

  13. Synthesis in land change science

    DEFF Research Database (Denmark)

    Magliocca, Nicholas R.; Rudel, Thomas K.; Verburg, Peter H.

    2015-01-01

    of these changes, land change science (LCS) draws on a wide array synthetic and meta-study techniques to generate global and regional knowledge from local case studies of land change. Here, we review the characteristics and applications of synthesis methods in LCS and assess the current state of synthetic research...... based on a meta-analysis of synthesis studies from 1995 to 2012. Publication of synthesis research is accelerating, with a clear trend toward increasingly sophisticated and quantitative methods, including meta-analysis. Detailed trends in synthesis objectives, methods, and land change phenomena......, synthesis methods based on local case studies will remain essential for generating systematic global and regional understanding of local land change for the foreseeable future, and multiple opportunities exist to accelerate and enhance the reliability of synthetic LCS research in the future. Demand...

  14. Inhibition of radiation degradation of polyolefins by hydroaromatics

    Science.gov (United States)

    Kubo, Junichi; Otsuhata, Kazushige

    Heavy hydroaromatics from petroleum (HHAP) which has evident inhibiting ability toward deterioration of hydrocarbon oils was added to high density polyethylene (PE) and isotactic polypropylene (PP), and the additive effects were examined. After the confirmation of the prominent effects to thermal oxidation of PE and PP, the additive effects to radiation degradation were tested by γ-ray and electron beam irradiations in air. The addition of HHAP was obviously effective in radiation degradation, and the crosslinking of PE was distinctly suppressed by HHAP.

  15. Blends of Amphiphilic, Hyperbranched Polyesters and Different Polyolefins

    NARCIS (Netherlands)

    Schmaljohann, D.; Pötschke, P.; Hässler, R.; Voit, B.I.; Froehling, P.E.; Mostert, B.; Loontjens, J.A.

    1999-01-01

    A hyperbranched polyester based on 3,5-dihydroxybenzoic acid was completely modified with dodecanoyl chloride to result in an amphiphilic, globular polymer, which has a polar core and a nonpolar outer sphere with the ability both to incorporate an organic dye and to interact with a nonpolar matrix.

  16. Radio-Oxidation in Polyolefins: Non-Stationary Kinetic Conditions

    International Nuclear Information System (INIS)

    Dely, N.

    2006-01-01

    In the last fifty years, many authors have been interested in the radio-oxidation processes occurring in polymers. The polymer degradation under ionising radiations in presence of dioxygen is well described by a radical chemistry. The radio-oxidation process occurs in three steps: the first one is the production of radicals P degree by interaction between the polymer and the ionising radiations; then radicals P degree react spontaneously with O 2 solved in the polymer giving a peroxy radical POO degree which attacks the polymer forming a hydroperoxide POOH and a new radical P degree (propagation). The third step corresponds to the termination step, that is bimolecular reactions between radicals. It is generally assumed that the stationary state is rapidly reached and consequently that the oxidation induced during the built-up period of the radical concentration can be neglected. However, to our best knowledge, the temporal evolution of radical concentrations before reaching the steady state regime has never been studied in details. We recently performed a complete study of oxygen consumption under electron irradiation for an EPDM elastomer. An analysis, as function of dose rate and oxygen pressure, and assuming steady state conditions, allowed extracting all the kinetic constants. Starting for these experimental data, we calculated the build-up of the radical concentration by solving numerically the differential equations with help of the Minichem code. We conclude that, in fact, the oxidation induced during the built-up period is negligible. In this paper we show that [P degree] could present a quasi-stationary plateau before reaching its stationary level. Consequently, the full radical time evolution is essentially determined by two characteristic times for reaching the quasi and stationary levels and three concentrations: [P degree] and [POO degree] at the stationary level and [P degree] at the quasi-stationary plateau. We show that realistic approximations can be found in order to establish analytical expressions of the temporal evolution of [P degree] and [POO degree]. The time evolution obtained analytically is in total agreement with the exact numerical solution. We want to emphasize that the analytical approximations show that the different parameters governing the build-up period are very simply linked to some kinetic constants of the radio-oxidation mechanism. This clearly shows that time-resolved experiments are a very attractive approach for determining accurately the kinetic parameters governing radio-oxidation

  17. Polyolefin-Nanocrystal Composites for Radiation Shielding, Phase I

    Data.gov (United States)

    National Aeronautics and Space Administration — EIC Laboratories Inc. is proposing a lightweight multifunctional polymer/nanoparticle composite for radiation shielding during long-duration lunar missions. Isolated...

  18. New multicomponent compatibilization system for polyolefin/polystyrene blends

    Czech Academy of Sciences Publication Activity Database

    Starý, Zdeněk; Kruliš, Zdeněk; Hromádková, Jiřina; Šlouf, Miroslav; Kotek, Jiří; Fortelný, Ivan

    2006-01-01

    Roč. 21, č. 3 (2006), s. 222-229 ISSN 0930-777X R&D Projects: GA AV ČR IBS4050008 Institutional research plan: CEZ:AV0Z40500505 Keywords : compatibilization * blends * mechanical properties Subject RIV: CD - Macromolecular Chemistry Impact factor: 0.563, year: 2006

  19. New Method for Online Observation of Growing Polyolefin Particles

    NARCIS (Netherlands)

    Pater, J.T.M.; Weickert, G.; van Swaaij, Willibrordus Petrus Maria

    2001-01-01

    In classical experimental research work on catalytic olefin polymerization, kinetics and powder properties are always determined as an average value over a large number of polymer particles. When studying the properties of the polymer, the powder has to be evacuated from the reactor system. This

  20. Point load effect on the buried polyolefin pipes lifetime

    Czech Academy of Sciences Publication Activity Database

    Majer, Z.; Hutař, Pavel; Frank, A.; Ševčík, Martin; Zouhar, Michal; Pinter, G.; Náhlík, Luboš

    2016-01-01

    Roč. 56, č. 1 (2016), s. 79-86 ISSN 0032-3888 R&D Projects: GA MŠk(CZ) ED1.1.00/02.0068 Institutional support: RVO:68081723 Keywords : INTERNAL-PRESSURE * PREDICTION * CRACK * STRESS * POLYETHYLENE * FAILURE * CONSTANT * GROWTH Subject RIV: JL - Materials Fatigue, Friction Mechanics Impact factor: 1.449, year: 2016 http://onlinelibrary.wiley.com/doi/10.1002/pen.24194/abstract

  1. Phenols and aromatic amines as thermal stabilizers in polyolefin processing

    Czech Academy of Sciences Publication Activity Database

    Pospíšil, Jan; Habicher, W. D.; Al-Malaika, S.; Zweifel, H.; Nešpůrek, Stanislav

    2001-01-01

    Roč. 176, - (2001), s. 55-63 ISSN 1022-1360. [International Conference on Polymer Modification, Degradation and Stabilization /1./. Palermo, 03.09.2000-07.09.2000] R&D Projects: GA AV ČR IAA1050901; GA MŠk ME 184; GA MŠk ME 372; GA AV ČR KSK4050111 Institutional research plan: CEZ:AV0Z4050913 Keywords : thermal stabilizers * phenols * aromatic amines Subject RIV: CD - Macromolecular Chemistry Impact factor: 0.634, year: 2001

  2. Microporous membranes from polyolefin-polyamide blend materials

    Czech Academy of Sciences Publication Activity Database

    Meier-Haack, J.; Valko, M.; Lunkwitz, K.; Bleha, Miroslav

    2004-01-01

    Roč. 163, 1-3 (2004), s. 215-221 ISSN 0011-9164. [Membrane Science and Technology Conference PERMEA 2003. Tatranské Matliare, 07.09.2003-11.09.2003] Institutional research plan: CEZ:AV0Z4050913 Keywords : microporous membranes * polypropylene polyamide blends * reactive extrusion Subject RIV: CD - Macromolecular Chemistry Impact factor: 1.057, year: 2004

  3. Reactive compatibilization of polyolefins using low molecular weight polybutadiene

    Czech Academy of Sciences Publication Activity Database

    Kruliš, Zdeněk; Horák, Zdeněk; Lednický, František; Pospíšil, Jan; Sufčák, M.

    1998-01-01

    Roč. 258, č. 4537 (1998), s. 63-68 ISSN 0003-3146 R&D Projects: GA ČR GA106/96/1377 Grant - others:Copernicus(XE) IC15-CT96-0731 Subject RIV: CD - Macromolecular Chemistry Impact factor: 0.488, year: 1998

  4. Reevaluating synthesis by biology.

    Science.gov (United States)

    Yadav, Vikramaditya G; Stephanopoulos, Gregory

    2010-06-01

    The two cornerstones of synthetic biology are the introduction of the new technology of chemical DNA synthesis and its subsequent emphasis on the use of standardized biological parts in the construction of genetic systems aimed at eliciting of desired cellular behavior. A number of high-impact applications have been proposed for this technology, notable among them being the biological synthesis of valuable compounds for chemical or pharmaceutical use. To this end, synthetic biologists propose assembling metabolic pathways in toto by combining genes isolated from a variety of sources. While pathway construction is similar to approaches established long ago by Metabolic Engineering, the two methods deviate significantly when it comes to pathway optimization. Synthetic biologists opt for gene-combinatorial methods whereby large numbers of pathways, comprising several combinations of genes from different sources, and their mutants, are evaluated in search for an optimal pathway configuration. Metabolic engineering, on the contrary, aims to optimize pathways by tuning the activity of the intermediate reaction steps. Both, rational methods based on kinetics and regulation, as well as combinatorial methods, typically in this order, are used to this end. We argue that a systematic approach consisting of fine-tuning the properties of individual pathway components, prominently enzymes, is a superior strategy to searches spanning large genetic spaces in engineering optimal microbes for the production of chemical and pharmaceutical products. Copyright 2010 Elsevier Ltd. All rights reserved.

  5. Synthesis of Lysophospholipids

    Directory of Open Access Journals (Sweden)

    Paola D’Arrigo

    2010-03-01

    Full Text Available New synthetic methods for the preparation of biologically active phospholipids and lysophospholipids (LPLs are very important in solving problems of membrane–chemistry and biochemistry. Traditionally considered just as second-messenger molecules regulating intracellular signalling pathways, LPLs have recently shown to be involved in many physiological and pathological processes such as inflammation, reproduction, angiogenesis, tumorogenesis, atherosclerosis and nervous system regulation. Elucidation of the mechanistic details involved in the enzymological, cell-biological and membrane-biophysical roles of LPLs relies obviously on the availability of structurally diverse compounds. A variety of chemical and enzymatic routes have been reported in the literature for the synthesis of LPLs: the enzymatic transformation of natural glycerophospholipids (GPLs using regiospecific enzymes such as phospholipases A1 (PLA1, A2 (PLA2 phospholipase D (PLD and different lipases, the coupling of enzymatic processes with chemical transformations, the complete chemical synthesis of LPLs starting from glycerol or derivatives. In this review, chemo-enzymatic procedures leading to 1- and 2-LPLs will be described.

  6. Oxygenates vs. synthesis gas

    Energy Technology Data Exchange (ETDEWEB)

    Kamil Klier; Richard G. Herman; Alessandra Beretta; Maria A. Burcham; Qun Sun; Yeping Cai; Biswanath Roy

    1999-04-01

    Methanol synthesis from H{sub 2}/CO has been carried out at 7.6 MPa over zirconia-supported copper catalysts. Catalysts with nominal compositions of 10/90 mol% and 30/70 mol% Cu/ZrO{sub 2} were used in this study. Additionally, a 3 mol% cesium-doped 10/90 catalyst was prepared to study the effect of doping with heavy alkali, and this promoter greatly increased the methanol productivity. The effects of CO{sub 2} addition, water injection, reaction temperature, and H{sub 2}/C0 ratio have been investigated. Both CO{sub 2} addition to the synthesis gas and cesium doping of the catalyst promoted methanol synthesis, while inhibiting the synthesis of dimethyl ether. Injection of water, however, was found to slightly suppress methanol and dimethyl ether formation while being converted to CO{sub 2} via the water gas shift reaction over these catalysts. There was no clear correlation between copper surface area and catalyst activity. Surface analysis of the tested samples revealed that copper tended to migrate and enrich the catalyst surface. The concept of employing a double-bed reactor with a pronounced temperature gradient to enhance higher alcohol synthesis was explored, and it was found that utilization of a Cs-promoted Cu/ZnO/Cr{sub 2}O{sub 3} catalyst as a first lower temperature bed and a Cs-promoted ZnO/Cr{sub 2}O{sub 3} catalyst as a second high-temperature bed significantly promoted the productivity of 2-methyl-1-propanol (isobutanol) from H{sub 2}/CO synthesis gas mixtures. While the conversion of CO to C{sub 2+} oxygenates over the double-bed configuration was comparable to that observed over the single Cu-based catalyst, major changes in the product distribution occurred by the coupling to the zinc chromite catalyst; that is, the productivity of the C{sub 1}-C{sub 3} alcohols decreased dramatically, and 2-methyl branched alcohols were selectively formed. The desirable methanol/2-methyl oxygenate molar ratios close to 1 were obtained in the present double

  7. Truncated borrelidin analogues: synthesis by sequential cross metathesis/olefination for the southern fragment and biological evaluation.

    Science.gov (United States)

    Gündemir-Durmaz, Tülay; Schmid, Fabian; El Baz, Yana; Häusser, Annette; Schneider, Carmen; Bilitewski, Ursula; Rauhut, Guntram; Garnier, Delphine; Baro, Angelika; Laschat, Sabine

    2016-09-21

    The construction of novel borrelidin analogues is reported in which the northern fragment is truncated to a simple hydroxyundecanecarboxylate and the original cyclopentanecarboxylic acid in the southern fragment is replaced with different six-membered rings. The required precursors were prepared by cross metathesis of the appropriate carbocycle-based homoallylic alcohol with crotonaldehyde followed by HWE olefination of the resulting enal with bromocyanophosphonate. The key aldehyde for intramolecular cross coupling was accessible by oxidation of the hydroxy group of the linked undecanecarboxylate unit. Grignard mediated macrocyclization finally yielded the borrelidin related products. The investigation is complemented by SAR studies and quantum-chemical calculations.

  8. Synthesis of 2-phosphaadamantane derivatives

    International Nuclear Information System (INIS)

    Zemlyanoi, V.N.; Aleksandrov, A.M.; Kukhar', V.P.

    1986-01-01

    The authors describe the synthesis and properties of 2-phosphadamantane derivatives. For the synthesis of 2-phosphaadamantane derivatives they decided to use the methodology of the synthesis of 2-thiaadamantane. The IR spectra were determined on CHCl 3 solutions with a Specord 711R spectrometer, the PMR spectra were determined on Tesla BS-467 (60 MHz) and Bruker WP-200 (200 MHz) spectrometers, external standard hexamethyldisiloxane, the 31 P NMR spectra were determined on Tesla BS-487 C (30 MHz) and Bruker WP-200 (81 MHz) spectrometers, external standard 85% phosphoric acid, and the mass spectra were determined on an MS-1302 spectrometer

  9. Synthesis of C-vinylpyrroles

    International Nuclear Information System (INIS)

    Sobenina, Lyubov N; Demenev, Andrei P; Mikhaleva, Albina I; Trofimov, Boris A

    2002-01-01

    The latest advances in the synthesis of C-vinylpyrroles are generalised and systematised. Methods for the synthesis based on reactions of acylpyrroles and dicarbonyl compounds or their synthetic equivalents are still of most importance. New promising methods for the synthesis of C-vinylpyrroles are considered, among them the reactions of alkenyl ketone oximes with acetylene in the KOH-DMSO system and base-catalysed condensation of pyrrolecarbodithioates, which have recently become available, with CH-acids. The bibliography includes 195 references.

  10. Hypericin: chemical synthesis and biosynthesis.

    Science.gov (United States)

    Huang, Lin-Fang; Wang, Zeng-Hui; Chen, Shi-Lin

    2014-02-01

    Hypericin is one of the most important phenanthoperylene quinones extracted mainly from plants of the genus Hypericum belonging to the sections Euhypericum and Campylosporus of Keller's classification. Widespread attention to the antiviral and anti-tumor properties of hypericin has spurred investigations of the chemical synthesis and biosynthesis of this unique compound. However, the synthetic strategies are challenging for organic and biological chemists. In this review, specific significant advances in total synthesis, semi-synthesis, and biosynthesis in the past decades are summarized. Copyright © 2014 China Pharmaceutical University. Published by Elsevier B.V. All rights reserved.

  11. Journal of Chemical Sciences | Indian Academy of Sciences

    Indian Academy of Sciences (India)

    More Details Abstract Fulltext PDF. pp 1831-1840 Regular Article. Study towards diversity oriented synthesis of optically active substituted cyclopentane fused carbocyclic and oxacyclic medium-sized rings: Competition between Grubbs-II catalyzed ring closing olefin metathesis and ring closing carbonyl-olefin metathesis.

  12. JCSC_128_12_1831_1840_SI.docx

    Indian Academy of Sciences (India)

    S Roy

    Study towards diversity oriented synthesis of optically active substituted cyclopentane fused carbocyclic and oxacyclic medium-sized rings: Competition between Grubbs-II catalyzed ring closing olefin metathesis and ring closing carbonyl-olefin metathesis. P CHAKRABORTY and S C ROY*. Department of Organic ...

  13. Synthesis of radium silicate

    International Nuclear Information System (INIS)

    Garibov, A.A; Agayev, T.N; Mansimov, Z.A

    2010-01-01

    Full text :One of the possible ways of implementation of the processes of molecular hydrogen radiologic of the elements in the differential heat of water as a catalyst for the collapse of the creation of a special nuclear reactors. A chemical process in radiation-4-oxide-silicon compounds, which is one of the radium, is of great importance. Research in the silicon-oxide-radiumun different activity-4 has been synthesized. As initial substances for the synthesis of tetra etiolate silicate and radium chloride solutions were used. At the same time to remove reaction products from the reaction intermediate in acetate acid was used. The intermediate product was reacted with ethyl alcohol ethyl acetate ether acetate acid that forms from the reaction of the temperature effect is broken. As a result, 4-oxide was initially pure silicon.

  14. The synthesis of clopidogrel

    Science.gov (United States)

    Huang, Yuanjun; Zhu, Qingxin

    2017-12-01

    Cardiac and cerebrovascular disease is a common disease. It is well recognized that antiplatelet agent is effective in the prevention and treatment of thrombosis. Clopidogrel is one of thieno pyridine derivatives, which can inhibit ADP-induced platelet aggregation. The preparation methods of Clopidogrel were reviewed and Clopidogrel was finally synthesized from 2-chlorobenzyl cyanide via bromination, condensation, hydrolyze, esterification, resolution, Finally with the sulfate, re-crystallization product of the target compound clopidogrel. The overall yield is 16%. Synthesis of the intermediate product and finally the structure of the product through ESI and 1H-NMR corroboration. The improved synthetic procedure has the advantage of low cost and is suitable for industrial production.

  15. Synthesis of cyclododeciptycene quinones.

    Science.gov (United States)

    Lou, Kaiyan; Prior, Allan M; Wiredu, Bernard; Desper, John; Hua, Duy H

    2010-12-15

    Cycloiptycenes are elusive and synthetically challenging molecules. We report the first synthesis of two substituted cyclododeciptycene tetraquinones via a sequence of intermolecular and intramolecular Diels-Alder reactions from cis,cis-heptiptycene tetraquinone 2 and substituted 7,16-dihydro-7,16-(o-benzeno)heptacenes 3. Heptiptycene tetraquinone 2 was made from triptycene bisquinone 4 and 1,4-dimethoxyanthracene in three steps, and 6,8,15,17-tetramethoxy-7,16-dihydro-7,16-(o-benzeno)heptacene (3a) was synthesized from triptycene bisquinone 4 and 1,4-dihydro-2,3-benzoxathiin-3-oxide in four steps. The structure of a cyclododeciptycene, 1a, was determined by a single-crystal X-ray analysis. The synthetic sequence is general and should allow the incorporation of various alkoxy and acetoxy substituents appended to the cycloiptycene framework.

  16. De Novo Glutamine Synthesis

    Science.gov (United States)

    He, Qiao; Shi, Xinchong; Zhang, Linqi; Yi, Chang; Zhang, Xuezhen

    2016-01-01

    Purpose: The aim of this study was to investigate the role of de novo glutamine (Gln) synthesis in the proliferation of C6 glioma cells and its detection with 13N-ammonia. Methods: Chronic Gln-deprived C6 glioma (0.06C6) cells were established. The proliferation rates of C6 and 0.06C6 cells were measured under the conditions of Gln deprivation along with or without the addition of ammonia or glutamine synthetase (GS) inhibitor. 13N-ammonia uptake was assessed in C6 cells by gamma counting and in rats with C6 and 0.06C6 xenografts by micro–positron emission tomography (PET) scanning. The expression of GS in C6 cells and xenografts was assessed by Western blotting and immunohistochemistry, respectively. Results: The Gln-deprived C6 cells showed decreased proliferation ability but had a significant increase in GS expression. Furthermore, we found that low concentration of ammonia was sufficient to maintain the proliferation of Gln-deprived C6 cells, and 13N-ammonia uptake in C6 cells showed Gln-dependent decrease, whereas inhibition of GS markedly reduced the proliferation of C6 cells as well as the uptake of 13N-ammoina. Additionally, microPET/computed tomography exhibited that subcutaneous 0.06C6 xenografts had higher 13N-ammonia uptake and GS expression in contrast to C6 xenografts. Conclusion: De novo Gln synthesis through ammonia–glutamate reaction plays an important role in the proliferation of C6 cells. 13N-ammonia can be a potential metabolic PET tracer for Gln-dependent tumors. PMID:27118759

  17. Vanillin Synthesis from 4-Hydroxybenzaldehyde

    Science.gov (United States)

    Taber, Douglass F.; Patel, Shweta; Hambleton, Travis M.; Winkel, Emma E.

    2007-01-01

    A regioselective, safe and efficient method for the synthesis of vanillin from 4-hydroxybenzaldehyde is being described. The vanillin derived from the process is cheap and can be used as a flavor or in the paper industry.

  18. Methyltrioctylammonium chloride catalysed sonochemical synthesis ...

    Indian Academy of Sciences (India)

    The greener, clean and efficient protocol for the synthesis of acridine diones derivatives has been achieved by reacting aromatic aldehyde, dimedone and amines using methyltrioctylammonium chloride (Aliquate 336) as a catalyst under ultrasonic irradiations.

  19. Green chemistry for nanoparticle synthesis.

    Science.gov (United States)

    Duan, Haohong; Wang, Dingsheng; Li, Yadong

    2015-08-21

    The application of the twelve principles of green chemistry in nanoparticle synthesis is a relatively new emerging issue concerning the sustainability. This field has received great attention in recent years due to its capability to design alternative, safer, energy efficient, and less toxic routes towards synthesis. These routes have been associated with the rational utilization of various substances in the nanoparticle preparations and synthetic methods, which have been broadly discussed in this tutorial review. This article is not meant to provide an exhaustive overview of green synthesis of nanoparticles, but to present several pivotal aspects of synthesis with environmental concerns, involving the selection and evaluation of nontoxic capping and reducing agents, the choice of innocuous solvents and the development of energy-efficient synthetic methods.

  20. Enzymatic synthesis of organophosphorus compounds

    International Nuclear Information System (INIS)

    Kolodiazhnyi, Oleg I

    2011-01-01

    Data on biocatalytic methods for the preparation of chiral organophosphorus compounds are generalized and described systematically. Various examples of enzymatic and microbiological synthesis of hydroxyphosphonates, aminophosphonates, phosphinites, phosphine oxides and tertiary phosphines are discussed. The bibliography includes 154 references.

  1. CLEAN CHEMICAL SYNTHESIS IN WATER

    Science.gov (United States)

    Newer green chemistry approach to accomplish chemical synthesis in water is summarized. Recent global developments pertaining to C-C bond forming reactions using metallic reagents and direct use of the renewable materials such as carbohydrates without derivatization are described...

  2. Gestural Control Of Wavefield synthesis

    DEFF Research Database (Denmark)

    Grani, Francesco; Di Carlo, Diego; Portillo, Jorge Madrid

    2016-01-01

    We present a report covering our preliminary research on the control of spatial sound sources in wavefield synthesis through gesture based interfaces. After a short general introduction on spatial sound and few basic concepts on wavefield synthesis, we presents a graphical application called sp......AAce which let users to con- trol real-time movements of sound sources by drawing tra- jectories on a screen. The first prototype of this application has been developed bound to WFSCollider, an open-source software based on Supercollider which let users control wavefield synthesis. The spAAce application has...... Wi- iMote game controller to “throw” sounding objects towards them. Aim of this project was to create a gestural interface for a game based on auditory cues only, and to investigate how convolution reverberation can affects people’s percep- tion of distance in a wavefield synthesis setup environment....

  3. Enzymatic synthesis of organophosphorus compounds

    Science.gov (United States)

    Kolodiazhnyi, Oleg I.

    2011-09-01

    Data on biocatalytic methods for the preparation of chiral organophosphorus compounds are generalized and described systematically. Various examples of enzymatic and microbiological synthesis of hydroxyphosphonates, aminophosphonates, phosphinites, phosphine oxides and tertiary phosphines are discussed. The bibliography includes 154 references.

  4. Essentials of inorganic materials synthesis

    CERN Document Server

    Rao, C N R

    2015-01-01

    This compact handbook describes all the important methods of synthesis employed today for synthesizing inorganic materials. Some features: Focuses on modern inorganic materials with applications in nanotechnology, energy materials, and sustainability Synthesis is a crucial component of materials science and technology; this book provides a simple introduction as well as an updated description of methods Written in a very simple style, providing references to the literature to get details of the methods of preparation when required

  5. Levulinic acid in organic synthesis

    International Nuclear Information System (INIS)

    Timokhin, Boris V; Baransky, V A; Eliseeva, G D

    1999-01-01

    Data concerning the methods of synthesis, chemical transformations and application of levulinic acid are analysed and generalised. The wide synthetic potential of levulinic acid, particularly as a key compound in the synthesis of various heterocyclic systems, saturated and unsaturated ketones and diketones, difficultly accessible acids and other compounds is demonstrated. The accessibility of levulinic acid from hexose-containing wood-processing and agricultural wastes is noted. The bibliography includes 260 references.

  6. Diamond Synthesis Employing Nanoparticle Seeds

    Science.gov (United States)

    Uppireddi, Kishore (Inventor); Morell, Gerardo (Inventor); Weiner, Brad R. (Inventor)

    2014-01-01

    Iron nanoparticles were employed to induce the synthesis of diamond on molybdenum, silicon, and quartz substrates. Diamond films were grown using conventional conditions for diamond synthesis by hot filament chemical vapor deposition, except that dispersed iron oxide nanoparticles replaced the seeding. This approach to diamond induction can be combined with dip pen nanolithography for the selective deposition of diamond and diamond patterning while avoiding surface damage associated to diamond-seeding methods.

  7. Principles of digital image synthesis

    CERN Document Server

    Glassner, Andrew S

    1995-01-01

    Image synthesis, or rendering, is a field of transformation: it changesgeometry and physics into meaningful images. Because the most popularalgorithms frequently change, it is increasingly important for researchersand implementors to have a basic understanding of the principles of imagesynthesis. Focusing on theory, Andrew Glassner provides a comprehensiveexplanation of the three core fields of study that come together to formdigital image synthesis: the human visual system, digital signalprocessing, and the interaction of matter and light. Assuming no more thana basic background in calculus,

  8. Isolation and synthesis of curcumin

    OpenAIRE

    Zetterström, Susanna

    2012-01-01

    The aim of this thesis was to evaluate pre-existing methods for isolation and synthesis of curcumin. Two different isolation methods were used, where only the extraction step differs from each other. To obtain pure curcumin, column chromatography was needed to separate the compound from its analogues. As for the isolation the synthesis was also carried out by two different methods, the first in a conventional way and the second one by using irradiation of microwaves. The result of the experim...

  9. Synthesis of ferroelectric nanostructures

    Energy Technology Data Exchange (ETDEWEB)

    Roervik, Per Martin

    2008-12-15

    The increasing miniaturization of electric and mechanical components makes the synthesis and assembly of nanoscale structures an important step in modern technology. Functional materials, such as the ferroelectric perovskites, are vital to the integration and utility value of nanotechnology in the future. In the present work, chemical methods to synthesize one-dimensional (1D) nanostructures of ferroelectric perovskites have been studied. To successfully and controllably make 1D nanostructures by chemical methods it is very important to understand the growth mechanism of these nanostructures, in order to design the structures for use in various applications. For the integration of 1D nanostructures into devices it is also very important to be able to make arrays and large-area designed structures from the building blocks that single nanostructures constitute. As functional materials, it is of course also vital to study the properties of the nanostructures. The characterization of properties of single nanostructures is challenging, but essential to the use of such structures. The aim of this work has been to synthesize high quality single-crystalline 1D nanostructures of ferroelectric perovskites with emphasis on PbTiO3 , to make arrays or hierarchical nanostructures of 1D nanostructures on substrates, to understand the growth mechanisms of the 1D nanostructures, and to investigate the ferroelectric and piezoelectric properties of the 1D nanostructures. In Paper I, a molten salt synthesis route, previously reported to yield BaTiO3 , PbTiO3 and Na2Ti6O13 nanorods, was re-examined in order to elucidate the role of volatile chlorides. A precursor mixture containing barium (or lead) and titanium was annealed in the presence of NaCl at 760 degrees Celsius or 820 degrees Celsius. The main products were respectively isometric nanocrystalline BaTiO3 and PbTiO3. Nanorods were also detected, but electron diffraction revealed that the composition of the nanorods was

  10. Synthesis of nanostructured polyaniline

    Science.gov (United States)

    Surwade, Sumedh P.

    The organization of my thesis is as follows: (a) Chapter III describes the synthesis of bulk quantities of polyaniline nanofibers in one step using a simple and versatile high ionic strength aqueous system (HCl/NaCl) that permits the use of pure H2O2 as a mild oxidant without any added metal or enzyme catalyst. Polyaniline nanofibers obtained are highly conducting, sigma˜1--5 S/cm, and spectroscopically similar to conventional polyaniline synthesized using stronger oxidants. The synthesis method is further extended to the synthesis of oligoanilines of controlled molecular weight, e.g., aniline tetramer, octamer, and hexadecamer. Microns long tetramer nanofibers are synthesized using this method. (b) Chapter IV describes the mechanism of nanofiber formation in polyaniline. It is proposed that the surfaces such as the walls of the reaction vessel and/or intentionally added surfaces play a dramatic role in the evolution of nanofibrillar morphology. Nucleation sites on surfaces promote the accumulation of aniline dimer that reacts further to yield aniline tetramer, which (surprisingly) is entirely in form of nanofibers and whose morphology is transcribed to the bulk by a double heterogeneous nucleation mechanism. This unexpected phenomenon could form the basis of nanofiber formation in all classes of precipitation polymerization systems. (c) Chapter V is the mechanistic study on the formation of oligoanilines during the chemical oxidation of aniline in weakly acidic, neutral or basic media using peroxydisulfate oxidant. It is proposed that the reaction proceeds via the intermediacy of benzoquinone monoimine that is formed as a result of a Boyland-Sims rearrangement of aniline. The initial role of peroxydisulfate is to provide a pathway for the formation of benzoquinone monoimine intermediate that is followed by a conjugate Michael-type addition reaction with aniline or sulfated anilines. The products isolated in pH 2.5--10.0 buffers are intermediate species at various

  11. Electrifying Organic Synthesis.

    Science.gov (United States)

    Wiebe, Anton; Gieshoff, Tile; Möhle, Sabine; Rodrigo, Eduardo; Zirbes, Michael; Waldvogel, Siegfried R

    2018-01-02

    The direct synthetic organic use of electricity is currently experiencing a renaissance. More synthetically oriented laboratories working in this area are exploiting both novel and more traditional concepts, paving the way to broader applications of this niche technology. As only electrons serve as reagents, the generation of reagent waste is efficiently avoided. Moreover, stoichiometric reagents can be regenerated and allow a transformation to be conducted in an electrocatalytic fashion. However, the application of electroorganic transformations is more than minimizing the waste footprint, it rather gives rise to inherently safe processes, reduces the number of steps of many syntheses, allows for milder reaction conditions, provides alternative means to access desired structural entities, and creates intellectual property (IP) space. When the electricity originates from renewable resources, this surplus might be directly employed as a terminal oxidizing or reducing agent, providing an ultra-sustainable and therefore highly attractive technique. This Review surveys recent developments in electrochemical synthesis that will influence the future of this area. © 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.

  12. Synthesis of P005091

    Directory of Open Access Journals (Sweden)

    Ping YU

    2016-06-01

    Full Text Available To improve the synthesis method of P005091 (1-(5-((2,3-dichlorophenyl thio-4-nitro-2-thienyl ethanone, with 2-chlorothiophene as the starting material, acetyl chloride as the acetylation reagent and aluminium trichloride as the catalyst, acetyl is introduced in the 5th position of 2-chlorothiophene to get 2-acetyl-5-chlorothiophene (compound 2, and the yield is 91%; then with concentrated sulfuric acid as solvent and mixed acid as nitrating agent, 5-acetyl-2-chloro-3-nitrothiophene (compound 3 is obtained by nitration reaction with compound 2, and the yield is 64%; thioetherfication reaction of compound 3 and 2,3-dichlorobenzenethiol in DMF solution under the function of potassium carbonate takes place to obtain the target product P005091, and the yield is 76%. The structure of P005091 is confirmed by mp, 1H-NMR, 13C-NMR and MS, and the overall yield is 44%. The improved method has the advantages of low cost, simple operation, and a milder reaction condition compared with the former references, avoiding using the reagent with higher toxicity, and high yield on the premise that the product purity is assured.

  13. Synthesis and Properties of New Polymer Having Hindered Phenol Antioxidants

    International Nuclear Information System (INIS)

    Kim, Taek Hyeon; Song, Yi Rang; Kim, Jae Nyoung

    2003-01-01

    Polymeric antioxidants was successfully prepared by the copolymerization of monomeric maleimide with MMA. The copolymers possess some stabilizing effect against thermal oxidation with oven aging in air at 120 .deg. C for 5 days and also have the some resistance to water extraction. It is well known that the addition of antioxidants is the most convenient and effective way to block the thermal oxidation of polyolefins. Hindered phenol antioxidants, which contain the 2,6-di-tert-butylphenol functional group, are very effective primary antioxidants. However, low molecular weight (MW) antioxidants are easily lost from the polymers by the physical loss such as migration, evaporation, and extraction by liquid. The effectiveness of low MW antioxidants is limited. Therefore a new trend for antioxidant development is to prepare antioxidant with higher MW. The copolymerization or homopolymerization of the functional monomer bearing hindered phenol antioxidants is a conventional method for preparing polymeric antioxidants

  14. Synthesis of ammonia using sodium melt

    OpenAIRE

    Kawamura, Fumio; Taniguchi, Takashi

    2017-01-01

    Research into inexpensive ammonia synthesis has increased recently because ammonia can be used as a hydrogen carrier or as a next generation fuel which does not emit CO2. Furthermore, improving the efficiency of ammonia synthesis is necessary, because current synthesis methods emit significant amounts of CO2. To achieve these goals, catalysts that can effectively reduce the synthesis temperature and pressure, relative to those required in the Haber-Bosch process, are required. Although severa...

  15. Stereocontrolled Syntheses of Seven-Membered Carbocycles by Tandem Allene Aziridination/[4+3] Reaction.

    Science.gov (United States)

    Gerstner, Nels C; Adams, Christopher S; Tretbar, Maik; Schomaker, Jennifer M

    2016-10-10

    A tandem allene aziridination/[4+3]/reduction sequence converts simple homoallenic sulfamates into densely functionalized aminated cycloheptenes, where the relative stereochemistry at five contiguous asymmetric centers can be controlled through the choice of the solvent and the reductant. The products resulting from this chemistry can be readily transformed into complex molecular scaffolds which contain up to seven contiguous stereocenters. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. Gold catalyzed carbocyclization of dienyl acetates to construct mutifunctionalized 3-vinyl cyclohexanol derivatives.

    Science.gov (United States)

    Zhu, Li-Li; Wang, Ya-Hui; Zhang, Yu-Xin; Li, Xiao-Xiao; Liu, Heng; Chen, Zili

    2011-01-21

    A convenient new method was developed to construct six-membered 3-vinylcyclohexanols (and piperidine products) and 6-oxabicyclo[3.2.1]octan-7-one derivatives with high diastereoselectivities from 1,6-dienyl acetates via gold catalysis. The reaction proceeded through the nucleophilic addition of the alkenes onto the allylic cation group via a 6-endo-trig process. The substrate's structure affected the configuration orientation of the allylic cation group in a boatlike transition state, which afforded either the trans-cyclohexanols or cis-piperidine derivatives.

  17. A versatile synthon for the preparation for the preparation of carbasugars and carbocyclic nucleosides:

    DEFF Research Database (Denmark)

    Johansen, Steen Karsk

    Der er i det sidste decennium været stor forskningsaktivitet i relation til at fremstille og undersøge egenskaber af nye kulhydrat mimics da enzyminhibitorer er interessante i mange biologisk sammenhænge.Den kemiske udfordringen er at fremstille sådanne molekyler i en optisk aktiv form. Dette kan...

  18. Stereoselective Hydrogenation and Ozonolysis of Iridoids. Conversion into Carbocyclic Nucleoside Analogues

    DEFF Research Database (Denmark)

    Franzyk, Henrik; Stermitz, Frank R.

    1999-01-01

    Stereoselective hydrogenation of the iridoids geniposide (9) and aucubin (19) was achieved by using the 1-methyl-1-methoxyethyl ether (MIP) as protecting group for the allylic alcohol, as it enhanced the stereoselectivity and prevented undesired hydrogenolysis. Ozonolysis of the hydrogenation...

  19. INDIUM AND ZINC MEDIATED ONE-ATOM CARBOCYCLE ENLARGEMENT IN WATER. (R822668)

    Science.gov (United States)

    AbstractSix-, seven-, eight-membered rings are enlarged by one carbon-atom into seven-, eight- and nine-membered ring derivatives respectively, via indium or zinc mediated reactions in aqueous medium.

  20. METAL-MEDIATED TWO-ATOM CARBOCYCLE ENLARGEMENT IN AQUEOUS MEDIUM. (R822668)

    Science.gov (United States)

    The perspectives, information and conclusions conveyed in research project abstracts, progress reports, final reports, journal abstracts and journal publications convey the viewpoints of the principal investigator and may not represent the views and policies of ORD and EPA. Concl...

  1. Stereoselective Hydrogenation and Ozonolysis of Iridoids. Conversion into Carbocyclic Nucleoside Analogues

    DEFF Research Database (Denmark)

    Franzyk, Henrik; Stermitz, Frank R.

    1999-01-01

    product from 9, adoxoside (11), with reductive work-up, afforded either a chiral lactone (25) or a chiral polyol (26), depending on the reduction conditions. Polyol 26 was subjected to protecting group manipulation and subsequent oxidation and reductions to yield cyclopentane building blocks (29......Stereoselective hydrogenation of the iridoids geniposide (9) and aucubin (19) was achieved by using the 1-methyl-1-methoxyethyl ether (MIP) as protecting group for the allylic alcohol, as it enhanced the stereoselectivity and prevented undesired hydrogenolysis. Ozonolysis of the hydrogenation...

  2. Efforts toward rapid construction of the cortistatin A carbocyclic core via enyne-ene metathesis

    KAUST Repository

    Baumgartner, Corinne

    2010-01-01

    Our efforts toward the construction of the carbocylic core of cortistatin A via an enyne-ene metathesis are disclosed. Interestingly, an attempted S N2 inversion of a secondary mesylate in our five-membered D-ring piece gave a product with retention of stereochemistry. © 2010 The Royal Society of Chemistry.

  3. Sustainable Process Synthesis-Intensification

    DEFF Research Database (Denmark)

    Babi, Deenesh Kavi; Holtbruegge, Johannes; Lutze, Philip

    2014-01-01

    Sustainable process design can be achieved by performing process synthesis and process intensification together. This approach first defines a design target through a sustainability analysis and then finds design alternatives that match the target through process intensification. A systematic......, multi-stage framework for process synthesis- intensification that identifies more sustainable process designs has been developed. At stages 1-2, the working scale is at the level of unit operations, where a base case design is identified and analyzed with respect to sustainability metrics. At stages 3......, a phenomena-based process synthesis method is applied, where the phenomena involved in each tasks are identified, manipulated and recombined to generate new and/or existing unit operations configured into flowsheets that are more sustainable from those found in the previous levels. An overview of the key...

  4. Synthesis through Trans-disciplinarity

    DEFF Research Database (Denmark)

    Hansen, Hanne Tine Ring

    2006-01-01

    , architecture and landscape provides a great architectural experience. Another is Jörn Utzon's church in Bagsvaerd, Denmark, where the treatment of construction, acoustics and daylight ingeniously fuses with the church's function and architectural expression, once again offering a unique architectural...... experience. In relation to ‘environmentally sustainable' architecture the importance of synthesis becomes even more apparent, however, as the success of the design depends on how, and if, a synthesis is achieved between technology and architectural design.[2] This understanding has led me to consider how...... synthesis is a requirement for creating successful ‘environmentally sustainable' architecture through the application of trans-disciplinarity, which leads to an increased awareness of the differences in decision-making as well as that of communication barriers between the different professions...

  5. Sustainable Process Synthesis-Intensification

    DEFF Research Database (Denmark)

    Babi, Deenesh Kavi; Holtbruegge, Johannes; Lutze, Philip

    2014-01-01

    Sustainable process design can be achieved by performing process synthesis and process intensification together. This approach first defines a design target through a sustainability analysis and then finds design alternatives that match the target through process intensification. A systematic, mu...... concepts and the framework are presented together with the results from a case study highlighting the application of the framework to the sustainable design of a production process for dimethyl carbonate.......Sustainable process design can be achieved by performing process synthesis and process intensification together. This approach first defines a design target through a sustainability analysis and then finds design alternatives that match the target through process intensification. A systematic......, multi-stage framework for process synthesis- intensification that identifies more sustainable process designs has been developed. At stages 1-2, the working scale is at the level of unit operations, where a base case design is identified and analyzed with respect to sustainability metrics. At stages 3...

  6. The KTH synthesis of singing

    Directory of Open Access Journals (Sweden)

    Johan Sundberg

    2006-01-01

    Full Text Available This is an overview of the work with synthesizing singing that has been carried out at the Speech Music Hearing Department, KTH since 1977. The origin of the work, a hardware synthesis machine, is described and some aspects of the control program, a modified version of a text-to-speech conversion system are reviewed. Three applications are described in which the synthesis system has paved the way for investigations of specific aspects of the singing voice. One concerns the perceptual relevance of the center frequency of the singer's formant, one deals with characteristics of an ugly voice, and one regards intonation. The article is accompanied by 18 sound examples, several of which were not published before. Finally, limitations and advantages of singing synthesis are discussed.

  7. Structural synthesis of parallel robots

    CERN Document Server

    Gogu, Grigore

    This book represents the fifth part of a larger work dedicated to the structural synthesis of parallel robots. The originality of this work resides in the fact that it combines new formulae for mobility, connectivity, redundancy and overconstraints with evolutionary morphology in a unified structural synthesis approach that yields interesting and innovative solutions for parallel robotic manipulators.  This is the first book on robotics that presents solutions for coupled, decoupled, uncoupled, fully-isotropic and maximally regular robotic manipulators with Schönflies motions systematically generated by using the structural synthesis approach proposed in Part 1.  Overconstrained non-redundant/overactuated/redundantly actuated solutions with simple/complex limbs are proposed. Many solutions are presented here for the first time in the literature. The author had to make a difficult and challenging choice between protecting these solutions through patents and releasing them directly into the public domain. T...

  8. Woodward's Synthesis of Vitamin B12

    Indian Academy of Sciences (India)

    The synthesis of this molecule was a landmark in organic synthesis. It involved the masterful control of shapes of molecules to create 9 chiral centres with known absolute and relative configurations. The concepts of absolute and induced asymmetric synthesis are here explained. Robert B. Woodward was one of the greatest ...

  9. STICS: surface-tethered iterative carbohydrate synthesis.

    Science.gov (United States)

    Pornsuriyasak, Papapida; Ranade, Sneha C; Li, Aixiao; Parlato, M Cristina; Sims, Charles R; Shulga, Olga V; Stine, Keith J; Demchenko, Alexei V

    2009-04-14

    A new surface-tethered iterative carbohydrate synthesis (STICS) technology is presented in which a surface functionalized 'stick' made of chemically stable high surface area porous gold allows one to perform cost efficient and simple synthesis of oligosaccharide chains; at the end of the synthesis, the oligosaccharide can be cleaved off and the stick reused for subsequent syntheses.

  10. Formal synthesis of naturally occurring norephedrine

    Indian Academy of Sciences (India)

    A concise and simple synthesis of 1-hydroxy-phenethylamine derivatives has been achieved following classical organic transformations using commercially available chiral pools. The said derivatives were explored for the synthesis of naturally occurring bio-active small molecules. Formal synthesis of norephedrine, virolin ...

  11. Ferroic materials synthesis and applications

    CERN Document Server

    Virk, Hardev Singh

    2015-01-01

    Ferroics is the generic name given to the study of ferromagnets, ferroelectrics, and ferroelastics. The basis of this study is to understand the large changes in physical characteristics that occur over a very narrow temperature range. In recent years, a new class of ferroic materials has been attracting increased interest. These multiferroics exhibit more than one ferroic property simultaneously in a single phase. The present volume: ""Ferroic Materials: Synthesis and Applications"" has ten Chapters, spread over areas as diverse as Magnetic Oxide Nanomaterials, Ferrites Synthesis, Hexaferrite

  12. Impaired glutathione synthesis in schizophrenia

    DEFF Research Database (Denmark)

    Gysin, René; Kraftsik, Rudolf; Sandell, Julie

    2007-01-01

    Schizophrenia is a complex multifactorial brain disorder with a genetic component. Convergent evidence has implicated oxidative stress and glutathione (GSH) deficits in the pathogenesis of this disease. The aim of the present study was to test whether schizophrenia is associated with a deficit...... of GSH synthesis. Cultured skin fibroblasts from schizophrenia patients and control subjects were challenged with oxidative stress, and parameters of the rate-limiting enzyme for the GSH synthesis, the glutamate cysteine ligase (GCL), were measured. Stressed cells of patients had a 26% (P = 0.......002) decreased GCL activity as compared with controls. This reduction correlated with a 29% (P schizophrenia in two...

  13. Sequential logic analysis and synthesis

    CERN Document Server

    Cavanagh, Joseph

    2007-01-01

    Until now, there was no single resource for actual digital system design. Using both basic and advanced concepts, Sequential Logic: Analysis and Synthesis offers a thorough exposition of the analysis and synthesis of both synchronous and asynchronous sequential machines. With 25 years of experience in designing computing equipment, the author stresses the practical design of state machines. He clearly delineates each step of the structured and rigorous design principles that can be applied to practical applications. The book begins by reviewing the analysis of combinatorial logic and Boolean a

  14. Tunable synthesis of copper nanotubes

    International Nuclear Information System (INIS)

    Kaniukov, E; Yakimchuk, D; Kozlovsky, A; Shlimas, D; Zdorovets, M; Kadyrzhanov, K

    2016-01-01

    Simple method of tunable synthesis of copper nanotubes based on template synthesis was developed. A comprehensive study of the structural, morphological and electrical characteristics of the obtained nanostructures was carried out. Characterization of structural features was made by methods of scanning electron microscopy, energy dispersive spectroscopy and X-ray diffractometry analysis. Evaluation of wall thickness is made by methods of gas permeability. Electrical conductivity of nanotubes was define in the study of their current-voltage characteristics. The possibility to control of copper nanotubes physical properties by variation of the deposition parameters was shown. (paper)

  15. A Short Synthesis of (+)-Cyclophellitol

    DEFF Research Database (Denmark)

    Hansen, Flemming Gundorph; Bundgaard, Eva; Madsen, Robert

    2005-01-01

    A new synthesis of (+)-cyclophellitol, a potent b-glucosidase inhibitor, has been completed in nine steps from D-xylose. The key transformations involve a zinc-mediated fragmentation of benzyl-protected methyl 5-deoxy-5-iodo-xylofuranoside followed by a highly diastereoselective indium-mediated c......-mediated coupling with ethyl 4-bromocrotonate. Subsequent ring-closing olefin metathesis, ester reduction, olefin epoxidation, and deprotection then afford the natural product. This constitutes the shortest synthesis of (+)-cyclophellitol reported to date....

  16. Synthesis of magnetic polymeric microspheres

    Energy Technology Data Exchange (ETDEWEB)

    Gervald, A Yu; Gritskova, Inessa A; Prokopov, Nikolai I [M.V. Lomonosov Moscow State Academy of Fine Chemical Technology, Moscow (Russian Federation)

    2010-05-13

    The key types of magnetic polymeric microspheres are considered. Methods of synthesis of different types of magnetic nanoparticles and of preparation of stable magnetic fluids on their basis are outlined. The overview of the methods for the manufacture of magnetic polymeric microspheres is presented. The effect of the synthesis conditions on the characteristics of magnetic polymeric microspheres such as the diameter and the particle size distribution and the content of magnetic material is discussed by particular examples. The application fields of magnetic polymeric microspheres are briefly surveyed.

  17. Synthesis of magnetic polymeric microspheres

    International Nuclear Information System (INIS)

    Gervald, A Yu; Gritskova, Inessa A; Prokopov, Nikolai I

    2010-01-01

    The key types of magnetic polymeric microspheres are considered. Methods of synthesis of different types of magnetic nanoparticles and of preparation of stable magnetic fluids on their basis are outlined. The overview of the methods for the manufacture of magnetic polymeric microspheres is presented. The effect of the synthesis conditions on the characteristics of magnetic polymeric microspheres such as the diameter and the particle size distribution and the content of magnetic material is discussed by particular examples. The application fields of magnetic polymeric microspheres are briefly surveyed.

  18. β-Enaminonitriles in heterocylic synthesis: Synthesis of new ...

    Indian Academy of Sciences (India)

    WINTEC

    gicides and solvatochromatic dyes. Recently, a num- ber of papers and patents concerning the importance of β-enaminonitriles in the synthesis of biologically active compounds, dihydropyridines analogous to nifedipine and amlodipine as potential calcium channel blockers in the treatment of angina and hypertension have ...

  19. The Effect of Synthesis Parameters on the Catalytic Synthesis of ...

    African Journals Online (AJOL)

    NJD

    Synthesis of Multiwalled Carbon Nanotubes using. Fe-Co/CaCO. 3. Catalysts. Sabelo D. Mhlangaa,b, Kartick C. Mondala,b, Robin Cartera,b, Michael J. Witcombb,c and Neil J. Covillea,b*. aMolecular Sciences Institute and School of Chemistry, University of the Witwatersrand, Johannesburg, WITS 2050, South Africa.

  20. Enantiomeric 3-deaza-1',6'-isoneplanocin and its 3-bromo analogue: Synthesis by the Ullmann reaction and their antiviral properties.

    Science.gov (United States)

    Liu, Chong; Chen, Qi; Schneller, Stewart W

    2016-02-01

    The 1',6'-isomer of neplanocin A possesses biological properties that have not been optimised through rationally conceived analogues. In that direction, this Letter reports the use of the Ullmann reaction to achieve enantiomeric 3-deaza-1',6'-isoneplanocin and 3-bromo-3-deaza-1',6'-isoneplanocin. These four compounds showed significant Ebola activity that is not specifically due to their inhibition of S-adenonosylhomocysteine hydrolase, as might have been expected for 3-deazaadenine carbocyclic nucleosides. For some members of this group, antiviral activity was also found against human cytomegalovirus, hepatitis B, norovirus, and measles. Copyright © 2015 Elsevier Ltd. All rights reserved.

  1. Plant mediated green synthesis: modified approaches

    Science.gov (United States)

    Das, Ratul Kumar; Brar, Satinder Kaur

    2013-10-01

    Plant mediated green synthesis of different metallic nanoparticles has emerged as one of the options for implementation of green chemistry principles, and successfully made an important contribution towards green nanotechnology. However, beyond the synthesis and application aspects, the science of green synthesis has carried some wrong perceptions in an unforeseen fashion. In this review, some of the key issues related to the green synthesis of metallic nanoparticles employing plants as reducing/capping agents have been addressed. Random selection of plants and its overall impact on the different aspects of green synthesis have been discussed. Emphasis is given to the setting of some standard selection criteria to be adopted for selecting a plant for use in green synthesis. How selection of a plant can positively or negatively influence both procedure and products of a green synthesis process is the prime concern of this article. In addition to selection, the key issue of biocompatibility associated with green synthesized metallic nanoparticles has been considered. Both selection of plant and biocompatibility were reconsidered for their minute details in terms of synthesis, analysis and data interpretation in the green synthesis approach. The key factors capable of fine tuning the core meaning of ``green'' in the synthesis of any metallic nanoparticles were taken into consideration. This article is an effort towards keeping the core meaning of green synthesis.

  2. Plant mediated green synthesis: modified approaches.

    Science.gov (United States)

    Das, Ratul Kumar; Brar, Satinder Kaur

    2013-11-07

    Plant mediated green synthesis of different metallic nanoparticles has emerged as one of the options for implementation of green chemistry principles, and successfully made an important contribution towards green nanotechnology. However, beyond the synthesis and application aspects, the science of green synthesis has carried some wrong perceptions in an unforeseen fashion. In this review, some of the key issues related to the green synthesis of metallic nanoparticles employing plants as reducing/capping agents have been addressed. Random selection of plants and its overall impact on the different aspects of green synthesis have been discussed. Emphasis is given to the setting of some standard selection criteria to be adopted for selecting a plant for use in green synthesis. How selection of a plant can positively or negatively influence both procedure and products of a green synthesis process is the prime concern of this article. In addition to selection, the key issue of biocompatibility associated with green synthesized metallic nanoparticles has been considered. Both selection of plant and biocompatibility were reconsidered for their minute details in terms of synthesis, analysis and data interpretation in the green synthesis approach. The key factors capable of fine tuning the core meaning of "green" in the synthesis of any metallic nanoparticles were taken into consideration. This article is an effort towards keeping the core meaning of green synthesis.

  3. Green chemistry for chemical synthesis

    Science.gov (United States)

    Li, Chao-Jun; Trost, Barry M.

    2008-01-01

    Green chemistry for chemical synthesis addresses our future challenges in working with chemical processes and products by inventing novel reactions that can maximize the desired products and minimize by-products, designing new synthetic schemes and apparati that can simplify operations in chemical productions, and seeking greener solvents that are inherently environmentally and ecologically benign. PMID:18768813

  4. Efficient synthesis of substituted dihydrotetraazapentacenes.

    Science.gov (United States)

    Seillan, Claire; Brisset, Hugues; Siri, Olivier

    2008-09-18

    We describe a versatile and very efficient synthesis of previously unknown substituted 5,14-dihydro-5,7,12,14-tetraazapentacenes (DHTAPs). A structural study by NMR spectroscopy showed that the conjugated pi-system of the pentacyclic skeleton rearranges depending on the electronic effect of the substituent(s).

  5. Analysis and synthesis of laughter

    Science.gov (United States)

    Sundaram, Shiva; Narayanan, Shrikanth

    2004-10-01

    There is much enthusiasm in the text-to-speech community for synthesis of emotional and natural speech. One idea being proposed is to include emotion dependent paralinguistic cues during synthesis to convey emotions effectively. This requires modeling and synthesis techniques of various cues for different emotions. Motivated by this, a technique to synthesize human laughter is proposed. Laughter is a complex mechanism of expression and has high variability in terms of types and usage in human-human communication. People have their own characteristic way of laughing. Laughter can be seen as a controlled/uncontrolled physiological process of a person resulting from an initial excitation in context. A parametric model based on damped simple harmonic motion to effectively capture these diversities and also maintain the individuals characteristics is developed here. Limited laughter/speech data from actual humans and synthesis ease are the constraints imposed on the accuracy of the model. Analysis techniques are also developed to determine the parameters of the model for a given individual or laughter type. Finally, the effectiveness of the model to capture the individual characteristics and naturalness compared to real human laughter has been analyzed. Through this the factors involved in individual human laughter and their importance can be better understood.

  6. Methyltrioctylammonium chloride catalysed sonochemical synthesis ...

    Indian Academy of Sciences (India)

    Methyltrioctylammonium chloride catalysed sonochemical synthesis of acridine diones. BHUPINDER KAUR and HARISH KUMAR. ∗. Department of Chemistry, Sant Longowal Institute of Engineering and Technology, Longowal 148 106, India e-mail: choprahk67@gmail.com. MS received 21 May 2012; revised 30 January ...

  7. SYNTHESIS, CHARACTERIZATION AND DENSITY FUNCTIONAL ...

    African Journals Online (AJOL)

    Preferred Customer

    KEY WORDS: Monoacyl aniline, Synthesis, Density functional theory, Rotation barrier. INTRODUCTION ... on the electron density in the phenyl ring and the respective accelerating and decelerating effects on the rate of ... compounds were determined using Nujol mulls and of liquids either in dichloromethane or chloroform ...

  8. Hydrothermal synthesis, characterization and luminescent ...

    Indian Academy of Sciences (India)

    Home; Journals; Bulletin of Materials Science; Volume 39; Issue 4. Hydrothermal synthesis, characterization and luminescent properties of lanthanide-doped NaLaF 4 nanoparticles. JIGMET LADOL HEENA KHAJURIA SONIKA KHAJURIA ... Keywords. Citric acid; X-ray diffraction; down-conversion emission; energy transfer.

  9. Methanol synthesis beyond chemical equilibrium

    NARCIS (Netherlands)

    van Bennekom, J. G.; Venderbosch, R. H.; Winkelman, J. G. M.; Wilbers, E.; Assink, D.; Lemmens, K. P. J.; Heeres, H. J.

    2013-01-01

    In commercial methanol production from syngas, the conversion is thermodynamically limited to 0.3-0.7 leading to large recycles of non-converted syngas. This problem can be overcome to a significant extent by in situ condensation of methanol during its synthesis which is possible nowadays due to the

  10. Total Synthesis of a Gene

    Indian Academy of Sciences (India)

    Home; Journals; Resonance – Journal of Science Education; Volume 17; Issue 12. Total Synthesis of a Gene. H G Khorana. Classics Volume 17 Issue 12 December 2012 pp 1174-1197 ... Author Affiliations. H G Khorana1. Professor of Biology and Chemestry, Massachusetts Institute of Technology, Cambridge 02139.

  11. Brassinosteroids: synthesis and biological activities

    Czech Academy of Sciences Publication Activity Database

    Oklešťková, Jana; Rárová, Lucie; Kvasnica, Miroslav; Strnad, Miroslav

    2015-01-01

    Roč. 14, č. 6 (2015), s. 1053-1072 ISSN 1568-7767 R&D Projects: GA MŠk(CZ) LO1204 Institutional support: RVO:61389030 Keywords : Brassinosteroids * Chemical synthesis * Plant biological activity Subject RIV: EB - Genetics ; Molecular Biology Impact factor: 2.686, year: 2015

  12. Synthesis of partially stabilized leucite

    Czech Academy of Sciences Publication Activity Database

    Kloužková, A.; Mrázová, M.; Kohoutková, Martina

    2007-01-01

    Roč. 68, 5-6 (2007), s. 1207-1210 ISSN 0022-3697 R&D Projects: GA MPO 2A-1TP1/063 Institutional research plan: CEZ:AV0Z40320502 Keywords : ceramics * chemical synthesis * X-ray diffraction Subject RIV: CA - Inorganic Chemistry Impact factor: 0.899, year: 2007

  13. Methyltrioctylammonium chloride catalysed sonochemical synthesis ...

    Indian Academy of Sciences (India)

    of the researchers because of their use as drugs for car- diovascular diseases, such as angina pectoris,7 hyper- tension,8 antitumour agents,9–11 DNA-binding moieties and DNA-intercalating anticancer drugs.12,13 There- fore, the synthesis of ... properties of ionic liquids they are emerging as a 'green reaction media'. ∗.

  14. Protein synthesis controls phosphate homeostasis.

    Science.gov (United States)

    Pontes, Mauricio H; Groisman, Eduardo A

    2018-01-01

    Phosphorus is an essential element assimilated largely as orthophosphate (Pi). Cells respond to Pi starvation by importing Pi from their surroundings. We now report that impaired protein synthesis alone triggers a Pi starvation response even when Pi is plentiful in the extracellular milieu. In the bacterium Salmonella enterica serovar Typhimurium , this response entails phosphorylation of the regulatory protein PhoB and transcription of PhoB-dependent Pi transporter genes and is eliminated upon stimulation of adenosine triphosphate (ATP) hydrolysis. When protein synthesis is impaired due to low cytoplasmic magnesium (Mg 2+ ), Salmonella triggers the Pi starvation response because ribosomes are destabilized, which reduces ATP consumption and thus free cytoplasmic Pi. This response is transient because low cytoplasmic Mg 2+ promotes an uptake in Mg 2+ and a decrease in ATP levels, which stabilizes ribosomes, resulting in ATP consumption and Pi increase, thus ending the response. Notably, pharmacological inhibition of protein synthesis also elicited a Pi starvation response in the bacterium Escherichia coli and the yeast Saccharomyces cerevisiae Our findings identify a regulatory connection between protein synthesis and Pi homeostasis that is widespread in nature. © 2018 Pontes and Groisman; Published by Cold Spring Harbor Laboratory Press.

  15. Phytochelatin synthesis in tomato cells

    International Nuclear Information System (INIS)

    Goldsbrough, P.; Gupta, S.; Huang, B.; Scheller, H.

    1987-01-01

    Tomato cells that are exposed to cadmium and other heavy metals synthesize phytochelatins (PCs), a family of peptides that bind heavy metals and are structurally related to glutathione (GSH). PCs have the structure (γ-glutamyl-cysteinyl) glycine; for PCs, n=2-10; GSH, n=1. GSH levels decline rapidly in tomato cells exposed to Cd 2+ . Buthionine sulfoximine (BSO), an inhibitor of GSH synthesis, prevents sustained synthesis of PC. However the addition of GSH to the medium of BSO-treated cells restores PC production. In vivo labeling studies indicate that 35 [S]-cysteine is incorporated into PC via GSH, rather than being added directly to GSH or pre-formed PC. Initial synthesis of PCs is not inhibited by cycloheximide. Tomato cell cultures that are tolerant of high levels of Cd 2+ contain large amounts of PCs. However, when sensitive and tolerant cells that have been grown in the absence of Cd 2+ are exposed to relatively low concentrations of Cd 2+ , they synthesize PCs at similar rates. These and other results suggest that, although PCs are necessary, increased PC synthesis is not sufficient for expression of the Cd 2+ tolerant phenotype

  16. Synthesis of Glucose Spiropiperazinone Derivatives

    OpenAIRE

    Vasiļjevs, D

    2013-01-01

    Piperazinone derivatives аге noticeable peptidometics; therefore, they сап replace peptides, such as RGD and Leu-enkephalin in different biological processes. Some piperazinone derivatives are anticoagulants, others act like neurotransmitters. Herein, we report an approach for the synthesis of поуеl piperazinone ring containing spiro-derivatives of glucose.

  17. Catalysis and prebiotic RNA synthesis

    Science.gov (United States)

    Ferris, James P.

    1993-01-01

    The essential role of catalysis for the origins of life is discussed. The status of the prebiotic synthesis of 2',5'- and 3'5'-linked oligomers of RNA is reviewed. Examples of the role of metal ion and mineral catalysis in RNA oligomer formation are discussed.

  18. SYNTHESIS AND CHARACTERIZATION OF FUNCTIONALIZED ...

    African Journals Online (AJOL)

    2016-07-30

    E-mail: b_mohtat@yahoo.com. This work is licensed under the Creative Commons ... Department of Chemistry, Islamic Azad University, Karaj Branch, Karaj, Iran. (Received July 30, 2016; revised ..... Chem. 2013, 9, 2846-2851. 7. Mohamed, K.S.; Soliman, M.A.; El-Remaily, M.A.A.; Abdel-Ghany, H. Eco-friendly synthesis of ...

  19. Northwest Forest Plan research synthesis.

    Science.gov (United States)

    Richard W. Haynes; Gloria E. Perez; [tech. eds.].

    2000-01-01

    This document synthesizes research accomplishments initiated and funded under the Northwest Forest Plan or the President’s Forest Plan (hereafter referred to as the Forest Plan) since its inception in 1994. Three major parts in this document cover, the context for this effort, eight Forest Plan research accomplishments, and a synthesis. The eight accomplishments...

  20. Multicomponent reactions in polymer synthesis.

    Science.gov (United States)

    Kakuchi, Ryohei

    2014-01-03

    More participants, yet efficient reactions: Multicomponent reactions (MCRs) have found application in polymer chemistry both in the synthesis of multifunctional monomers and in post-polymerization modification. Examples include the Passerini three-component reaction, the Ugi four-component reaction, and the copper-catalyzed MCR. Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  1. IONOTHERMAL SYNTHESIS, STRUCTURES AND SUPRAMOLE

    African Journals Online (AJOL)

    Preferred Customer

    2Department of Chemistry, University of Aveiro, CICECO, 3810-193 Aveiro, Portugal. (Received October 14 ... The principal feature of ionothermal synthesis is that the ionic liquids (ILs) act as both the “designed” green solvents ... purification except [EMI]Br. [EMI]Br was synthesized from the reaction of ethylbromide with.

  2. Green chemistry for chemical synthesis

    OpenAIRE

    Li, Chao-Jun; Trost, Barry M.

    2008-01-01

    Green chemistry for chemical synthesis addresses our future challenges in working with chemical processes and products by inventing novel reactions that can maximize the desired products and minimize by-products, designing new synthetic schemes and apparati that can simplify operations in chemical productions, and seeking greener solvents that are inherently environmentally and ecologically benign.

  3. Green chemistry for chemical synthesis.

    Science.gov (United States)

    Li, Chao-Jun; Trost, Barry M

    2008-09-09

    Green chemistry for chemical synthesis addresses our future challenges in working with chemical processes and products by inventing novel reactions that can maximize the desired products and minimize by-products, designing new synthetic schemes and apparati that can simplify operations in chemical productions, and seeking greener solvents that are inherently environmentally and ecologically benign.

  4. Synthesis of [14C] alaproclate

    International Nuclear Information System (INIS)

    Gawell, Lars

    1986-01-01

    The synthesis of carbon-14 labelled alaproclate from [2- 14 C]acetone in three steps is described. The label is introduced by the reaction of a benzylic Grignard reagent with the ketone yielding a tertiary alcohol. Subsequent esterification with an α-bromocarboxylic acid chloride and amination produced the title compound in a 13% overall radiochemical yield. (author)

  5. The Total Synthesis of Chlorophyll

    Indian Academy of Sciences (India)

    Home; Journals; Resonance – Journal of Science Education; Volume 19; Issue 7. The Total Synthesis of Chlorophyll. Setty Mallikarjuna Babu Subramania Ranganathan. General Article Volume 19 Issue 7 July 2014 pp 645-648. Fulltext. Click here to view fulltext PDF. Permanent link:

  6. Organic Synthesis using Clay Catalysts

    Indian Academy of Sciences (India)

    Home; Journals; Resonance – Journal of Science Education; Volume 7; Issue 1. Organic Synthesis using Clay Catalysts - Clays for 'Green Chemistry'. Gopalpur Nagendrappa. General Article Volume 7 Issue 1 January 2002 pp 64-77. Fulltext. Click here to view fulltext PDF. Permanent link:

  7. Hydrothermal synthesis, characterization and luminescent ...

    Indian Academy of Sciences (India)

    Home; Journals; Bulletin of Materials Science; Volume 39; Issue 4. Hydrothermal synthesis, characterization and luminescent properties of lanthanide-doped NaLaF 4 nanoparticles. JIGMET LADOL HEENA KHAJURIA SONIKA KHAJURIA HAQ NAWAZ SHEIKH. Volume 39 Issue 4 August 2016 pp 943-952 ...

  8. The Total Synthesis of Strychnine

    Indian Academy of Sciences (India)

    IAS Admin

    The Total Synthesis of Strychnine. Edited by Setty Mallikarjuna Babu and Subramania Ranganathan. Keywords. Strychnine. N. N. O. H. H. H. H. O. H. Strychnine! No other molecule has captured the popular imagina- tion as strychnine, perhaps because thousands of writers of fiction have used it to dispatch the recipient and ...

  9. SYNTHESIS, STRUCTURE AND PHOTOLUMINESCENCE OF ...

    African Journals Online (AJOL)

    Preferred Customer

    dimensional supramolecular framework. ... The growing interest in the field of the crystal engineering of inorganic-organic hybrid materials .... Synthesis, structure and photoluminescence of (HgCl3)n(C6NO2H6)n(C6NO2H5)n nH2O. Bull. Chem.

  10. Haber Process for Ammonia Synthesis

    Indian Academy of Sciences (India)

    Home; Journals; Resonance – Journal of Science Education; Volume 16; Issue 12. Haber Process for Ammonia Synthesis. Jayant M Modak. Volume 16 Issue 12 December 2011 pp 1159-1167. Fulltext. Click here to view fulltext PDF. Permanent link: https://www.ias.ac.in/article/fulltext/reso/016/12/1159-1167. Keywords.

  11. Solid-phase peptide synthesis

    DEFF Research Database (Denmark)

    Jensen, Knud Jørgen

    2013-01-01

    This chapter provides an introduction to and overview of peptide chemistry with a focus on solid-phase peptide synthesis. The background, the most common reagents, and some mechanisms are presented. This chapter also points to the different chapters and puts them into perspective....

  12. Microstructured Reactors for Electroorganic Synthesis

    Czech Academy of Sciences Publication Activity Database

    Bouzek, K.; Jiřičný, Vladimír; Kodým, R.; Křišťál, Jiří; Bystroň, T.

    2010-01-01

    Roč. 55, č. 7 (2010), s. 8172-8181 ISSN 0013-4686. [Annual Meeting of ISE /60./. Beijing, 16.08.2009-21.08.2009] Institutional research plan: CEZ:AV0Z40720504 Keywords : microstructured reactor * bipolar * electroorganic synthesis Subject RIV: CI - Industrial Chemistry, Chemical Engineering Impact factor: 3.642, year: 2010

  13. Synthesis of Polycyclic Natural Products

    Energy Technology Data Exchange (ETDEWEB)

    Nguyen, Tuan Hoang [Iowa State Univ., Ames, IA (United States)

    2003-01-01

    With the continuous advancements in molecular biology and modern medicine, organic synthesis has become vital to the support and extension of those discoveries. The isolations of new natural products allow for the understanding of their biological activities and therapeutic value. Organic synthesis is employed to aid in the determination of the relationship between structure and function of these natural products. The development of synthetic methodologies in the course of total syntheses is imperative for the expansion of this highly interdisciplinary field of science. In addition to the practical applications of total syntheses, the structural complexity of natural products represents a worthwhile challenge in itself. The pursuit of concise and efficient syntheses of complex molecules is both gratifying and enjoyable.

  14. Stereoselective Halogenation in Natural Product Synthesis.

    Science.gov (United States)

    Chung, Won-jin; Vanderwal, Christopher D

    2016-03-24

    At last count, nearly 5000 halogenated natural products have been discovered. In approximately half of these compounds, the carbon atom to which the halogen is bound is sp(3) -hybridized; therefore, there are an enormous number of natural products for which stereocontrolled halogenation must be a critical component of any synthesis strategy. In this Review, we critically discuss the methods and strategies used for stereoselective introduction of halogen atoms in the context of natural product synthesis. Using the successes of the past, we also attempt to identify gaps in our synthesis technology that would aid the synthesis of halogenated natural products, as well as existing methods that have not yet seen application in complex molecule synthesis. The chemistry described herein demonstrates yet again how natural products continue to provide the inspiration for critical advances in chemical synthesis. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  15. Physical synthesis of quantum circuits using templates

    Science.gov (United States)

    Mirkhani, Zahra; Mohammadzadeh, Naser

    2016-10-01

    Similar to traditional CMOS circuits, quantum circuit design flow is divided into two main processes: logic synthesis and physical design. Addressing the limitations imposed on optimization of the quantum circuit metrics because of no information sharing between logic synthesis and physical design processes, the concept of " physical synthesis" was introduced for quantum circuit flow, and a few techniques were proposed for it. Following that concept, in this paper a new approach for physical synthesis inspired by template matching idea in quantum logic synthesis is proposed to improve the latency of quantum circuits. Experiments show that by using template matching as a physical synthesis approach, the latency of quantum circuits can be improved by more than 23.55 % on average.

  16. Environment and hydroelectricity colloquium - Synthesis

    International Nuclear Information System (INIS)

    Aelbrecht, Denis; Abadie, Marc; Baril, Dominique; Delacoux, Jean-Yves; Delaunay, Alexis; Loudiere, Daniel; Penalba, Anne; Pont, Didier; Rocq, Sylvie; Roult, Didier; Sheibani, Neda; Thevenet, Regis; Weisrock, Ghislain

    2010-10-01

    This document proposes a synthesis of a colloquium dedicated to the interactions between hydroelectric installations and the environment. The four sessions respectively addressed the impacts of hydroelectric installations on ecosystems and more particularly on pisciculture populations (strategies for migration restoration, development of fish-friendly turbines), the sedimentary management of hydroelectric installations, the implementation of the Water Framework European Directive (Austrian experience, biological assessment criteria), and examples of environmental integration of existing or projected installations

  17. Macrocyclic cyclodiphosphazane : synthesis of chalcogen ...

    Indian Academy of Sciences (India)

    VITTHALRAO S KASHID

    2017-09-06

    Sep 6, 2017 ... Abstract. The synthesis of a Schiff base-appended macrocycle [{P(μ-tBuN)}2(O − m − C6H4CHNCH2)2]2. (1) containing cyclodiphosphazane moieties is described. Reactions of 1 with H2O2 and elemental selenium yielded derivatives tetrakis(oxide) [{P(O)(μ-tBuN)}2(O − m − C6H4CHNCH2)2]2 (2) and.

  18. Expertise synthesis on the CSPE

    International Nuclear Information System (INIS)

    Blonde, G.; Poizat, F.

    2008-01-01

    This document presents a synthesis of the results of an expertise realized on the CSPE, the compensation tax of the electric public service. This tax concerns the management of the electricity production additional costs in isolated areas, the solidarity, a policy to favor the energy efficiency and the renewable energies. The document explains the historical aspects of the tax elaboration, its financial importance, the consequences and the impacts on the competition. (A.L.B.)

  19. Asymmetric Synthesis of Apratoxin E.

    Science.gov (United States)

    Mao, Zhuo-Ya; Si, Chang-Mei; Liu, Yi-Wen; Dong, Han-Qing; Wei, Bang-Guo; Lin, Guo-Qiang

    2016-10-21

    An efficient method for asymmetric synthesis of apratoxin E 2 is described in this report. The chiral lactone 8, recycled from the degradation of saponin glycosides, was utilized to prepare the non-peptide fragment 6. In addition to this "from nature to nature" strategy, olefin cross-metathesis (CM) was applied as an alternative approach for the formation of the double bond. Moreover, pentafluorophenyl diphenylphosphinate was found to be an efficient condensation reagent for the macrocyclization.

  20. A Sustainable Multicomponent Pyrimidine Synthesis.

    Science.gov (United States)

    Deibl, Nicklas; Ament, Kevin; Kempe, Rhett

    2015-10-14

    Since alcohols are accessible from indigestible biomass (lignocellulose), the development of novel preferentially catalytic reactions in which alcohols are converted into important classes of fine chemicals is a central topic of sustainable synthesis. Multicomponent reactions are especially attractive in organic chemistry as they allow the synthesis of large libraries of diversely functionalized products in a short time when run in a combinatorial fashion. Herein, we report a novel, regioselective, iridium-catalyzed multicomponent synthesis of pyrimidines from amidines and up to three (different) alcohols. This reaction proceeds via a sequence of condensation and dehydrogenation steps which give rise to selective C-C and C-N bond formations. While the condensation steps deoxygenate the alcohol components, the dehydrogenations lead to aromatization. Two equiv of hydrogen and water are liberated in the course of the reactions. PN5P-Ir-pincer complexes, recently developed in our laboratory, catalyze this sustainable multicomponent process most efficiently. A total of 38 different pyrimidines were synthesized in isolated yields of up to 93%. Strong points of the new protocol are its regioselectivity and thus the immediate access to pyrimidines that are highly and unsymmetrically decorated with alkyl or aryl substituents. The combination of this novel protocol with established methods for converting alcohols to nitriles now allows to selectively assemble pyrimidines from four alcohol building blocks and 2 equiv of ammonia.

  1. Zeolite membranes for efficient synthesis of biofuels

    OpenAIRE

    Sandström, Linda

    2009-01-01

    The greenhouse effect and the limited fossil oil resources have increased the demand of renewable fuels. Zeolite membranes have potential applications in numerous separation processes, and could be useful in the development of efficient processes for renewable fuel production. Methanol synthesis from synthesis gas is equilibrium limited, and continuous removal of products in a zeolite membrane reactor could improve the productivity of a conventional methanol synthesis process. In this work, m...

  2. Automatic Synthesis of Multilevel Combinational Logic

    DEFF Research Database (Denmark)

    Andersen, Anders C.; Madsen, Jan; Madsen, J.R.

    1989-01-01

    This paper describes a system for the synthesis of multilevel combinational logic, transforming functional description into mask layout. The system includes a logic synthesis part, partly consisting of tools developed at Eindhoven University of Technology, which has been interfaced to the layout ...... synthesis part in the CATOE-system, developed at the DesignCenter of Electronics Institute. The various steps in the transformation are presented together with a complete design example, implementing a multi-output combinational decoder function....

  3. Synthesis by plasma of halogenated poly anilines

    International Nuclear Information System (INIS)

    Enriquez, M.A.; Olayo, M.G.; Cruz, G.J.

    2002-01-01

    In this work polymerization by plasma of aniline with iodine and chlorine bonded chemically to the aniline ring were realized. The results of the synthesis and characterizations are compared with those ones obtained starting from the poly aniline synthesis (P An) doped with iodine, where the dopant was aggregated in the moment of the polymerization. The objective is to study the dopant behavior in the synthesis by plasma in function of the properties of these polymers. (Author)

  4. Matrix-assisted peptide synthesis on nanoparticles.

    Science.gov (United States)

    Khandadash, Raz; Machtey, Victoria; Weiss, Aryeh; Byk, Gerardo

    2014-09-01

    We report a new method for multistep peptide synthesis on polymeric nanoparticles of differing sizes. Polymeric nanoparticles were functionalized via their temporary embedment into a magnetic inorganic matrix that allows multistep peptide synthesis. The matrix is removed at the end of the process for obtaining nanoparticles functionalized with peptides. The matrix-assisted synthesis on nanoparticles was proved by generating various biologically relevant peptides. Copyright © 2014 European Peptide Society and John Wiley & Sons, Ltd.

  5. Shape-Controlled Gold Nanoparticle Synthesis

    Science.gov (United States)

    2013-09-01

    Shankar, S. S.; Bhargava, S.; Sastry, M. Synthesis of Gold Nanospheres and Nanotriangles by the Turkevich Approach. Journal of Nanoscience and...Accounts of Chemical Research 2008, 41, 1587–1595. 22. Sun, Y.; Xia, Y. Shape-Controlled Synthesis of Gold And Silver Nanoparticles. Science...N.; Griep, M. H.; and Karna, S. P. Chemical vs. Sonochemical Synthesis and Characterization of Silver , Gold, and Hybrid Nanoparticles; ARL-TR-5764

  6. New Hybrid Route to Biomimetic Synthesis

    National Research Council Canada - National Science Library

    Morse, Daniel

    2003-01-01

    To develop economical low-temperature routes to biomimetic synthesis of high-performance composite materials, with control of composition and structure based on the molecular mechanisms controlling...

  7. Quest for the chemical synthesis of proteins.

    Science.gov (United States)

    Engelhard, Martin

    2016-05-01

    The chemical synthesis of proteins has been the wish of chemists since the early 19th century. There were decisive methodological steps necessary to accomplish this aim. Cornerstones were the introduction of the Z-protecting group of Bergmann and Zervas, the development of Solid-phase Peptide Synthesis of Merrifield, and the establishment of Native Chemical Ligation by Kent. Chemical synthesis of proteins has now become generally applicable technique for the synthesis of proteins with tailor made properties which can be applied not only in vitro but also in vivo .Copyright © 2016 European Peptide Society and John Wiley & Sons, Ltd. Copyright © 2016 European Peptide Society and John Wiley & Sons, Ltd.

  8. Synthesis of carbasugars from aldonolactones, part III - A study on the allylic substitution of (1R,5R,8R)- and (1R,5R,8S)-8-hydroxy-2-oxabicyclo[3.3.0]oct-6-en-3-one derivatives - Preparation of (1S,2R,3R)-9-[2-hydroxy-3-(2-hydroxyethyl)cyclopent-4-en-1-yl]-9H-adenine

    DEFF Research Database (Denmark)

    Johansen, Steen Karsk; Lundt, Inge

    2001-01-01

    with these nucleophiles. Additionally, Mitsunobu substitution of (1R,5R,8R)-8-hydroxy-2-oxabicyclo[3.3.0]oct-B-en-3-one (3) with 6-chloropurine, followed by reduction of the lactone moiety and treatment with Liquid ammonia, gave the carbocyclic nucleoside (1S,2R,3R)-9-[2-hydroxy-3-(2-hydroxyethyl)cyclopent-4-en-1-yl]-9H...

  9. Astrobiology - The New Synthesis

    Science.gov (United States)

    Sik, A.; Simon, T.

    á vált sötétebb helyekre való költöztetése: mélyen a föld alá helyezik, a forró vulkáni kőzetek hasadékaiba, ahol bőségesen találhatott magának ként, vasat, hidrogént és szenet. A genetikai bizonyítékok alapján a hő- és mélységkedvelők es- 4 nek legközelebb az egyetemes őshöz. [16]. The synthesis Mindezek alapján a földi extremofilek vizsgálata során deríthetjük ki, hogy más égitesteken (egyelőre a Naprendszerben) hol kell keresnünk az életet, és mit kell keresnünk a planetológiai kutatások során egyre jobban megismert szélsőséges környezetekben. Segítségükkel megtudhatjuk, melyek azok az alak- tani, geokémiai, esetleg biokémiai jegyek, amelyek életre utalhatnak; melyek az élet azon alapvető jellemzői, amelyek elég általánosak és biztonsággal kimu- tathatók, milyen műszerekkel kell felszerelnünk a jövő űrszondáit, milyen módszereket kell alkalmaznunk, hogy sikerrel kutathassunk a Földön kívüli élet után. References [1] H. Hargitai et. al., XXXIII. LPSC (2002), Houston, #1261; [2] Origins Roadmap, 2000, JPL; [3] http://www.obspm.fr/encycl/catalog.html [4] http://www.physics.sfsu.edu/~gmarcy/planetsearch/ upsand/upsand.html [5] http://tpf.jpl.nasa.gov/ [6] A. Kereszturi, and A. Sik, XXXI. LPSC (2000), Houston, #1216; [7] S. W. Squyres et. al. (1992) in H. H. Kieffer, et. al.: Mars, University of Arizona Press, Tucson, 523-554; [8] http://www.jpl.nasa.gov/europaorbiter/ [9] www.nineplanets.org [10] http://www.jpl.nasa.gov/cassini/ [11] http://www- curator.jsc.nasa.gov/curator/antmet/ marsmets/alh84001/sample.htm [12] P. Davies: The fifth miracle - The search for the origin of life (1998), Orion; [13] M. T. Madigan and B. L. Marrs: Extremophiles, Scientific American (1997), 276, 82-87; [14] J. A. Lake et al.: Methanococcus Genome, Science (1996), 274, 901-905; [15] N. C. Kyrpides and G. J. Olsen: Archaeal and bacterial hyperthermophiles: Horizontal gene exchange or common ancestry?, Trends in

  10. Web-Mediated Knowledge Synthesis for Educators

    Science.gov (United States)

    DeSchryver, Michael

    2015-01-01

    Ubiquitous and instant access to information on the Web is challenging what constitutes 21st century literacies. This article explores the notion of Web-mediated knowledge synthesis, an approach to integrating Web-based learning that may result in generative synthesis of ideas. This article describes the skills and strategies that may support…

  11. Heteropolyacids in synthesis of benzoyl hydrazone derivatives

    Directory of Open Access Journals (Sweden)

    Sodeh Sadjadi

    2009-12-01

    Full Text Available Keggin type of heteropolyacids as green reusable and efficient catalyst was used in the synthesis of benzoyl hydrazones from reaction of benzoic acid hydrazide and aldehyde and ketone derivatives. The synthesis of N-acetyl and N-benzoyl derivatives has also been performed by the reaction of obtained benzoyl hydrazones with acylcholorides in presence of this kind of heteropolyacids.

  12. Synthesis and characterization of saturated polyester and ...

    Indian Academy of Sciences (India)

    Synthesis and characterization of saturated polyester and nanocomposites derived from glycolyzed PET waste ... construction industries. PET is widely used in the packaging of beverages and drugs. ... ing the synthesis of saturated polyester (from GPET waste). This has been done for the estimation of the maximum. 277 ...

  13. Natural Synthesis: Where culture met academics | Chinyere ...

    African Journals Online (AJOL)

    This study attempts a detailed analysis of Natural Synthesis, the first meeting point of culture and academics in Nigeria. The study contextualized Natural Synthesis and the Nigerian traditional art and culture in relations to its transformation through the proponents of the philosophy. It discusses in details the genesis of the ...

  14. Alum an Efficient Catalyst for Erlenmeyer Synthesis

    African Journals Online (AJOL)

    NICO

    found to be useful precursors for the synthesis of amino acids,2 peptides,3 and ... tuted imidazoles,21h etc. However, there are no examples of the use of alum as a catalyst for the synthesis of azlactone deriva- tives. 2. Result and Discussion .... 12 P.S. Rao and R.V. Venkataratnam, Indian J. Chem, 1994, 33B, 984–985.

  15. Synthesis of Lipophilic Guanine N-9 Derivatives

    DEFF Research Database (Denmark)

    Wamberg, Michael C; Pedersen, Pernille L; Löffler, Philipp M G

    2017-01-01

    the synthesis of five new guanine-N9 derivatives bearing alkyl chains with different attachment chemistries, exploiting a synthesis pathway that allows a flexible choice of hydrophobic anchor moiety. In this study, these guanine derivatives were functionalized with C10 chains for insertion into decanoic acid...

  16. Urea synthesis in patients with chronic pancreatitis

    DEFF Research Database (Denmark)

    Hamberg, Ole; Andersen, Vibeke; Sonne, J

    2001-01-01

    Up-regulation of urea synthesis by amino acids and dietary protein intake may be impaired in patients with chronic pancreatitis (CP) due to the reduced glucagon secretion. Conversely, urea synthesis may be increased as a result of the chronic inflammation. The aims of the study were to determine...

  17. Combustion synthesis and photoluminescence study of silicate ...

    Indian Academy of Sciences (India)

    Silicate based bioceramics are promising candidates as biomaterials for tissue engineering. The combustion synthesis method provides control on the morphology and particle size of the synthesized material. This paper discusses the combustion synthesis of akermanite (Ca2MgSi2O7 and Sr2MgSi2O7), which has been ...

  18. Woodward's Synthesis of Vitamin B12

    Indian Academy of Sciences (India)

    Woodward's Synthesis of Vitamin B12. Adil Ghani Khan is a final year student of BSc. (Honours) in Chemistry at. St. Stephen's College,. Delhi University. S V Eswaran is an accomplished Organic. Chemist and principal of. Deshbandhu College,. Delhi University. Keywords. Asymmetric synthesis, chira!. Adil Ghani Khan and ...

  19. Swelling of rat hepatocytes stimulates glycogen synthesis

    NARCIS (Netherlands)

    Baquet, A.; Hue, L.; Meijer, A. J.; van Woerkom, G. M.; Plomp, P. J.

    1990-01-01

    In hepatocytes from fasted rats, several amino acids are known to stimulate glycogen synthesis via activation of glycogen synthase. The hypothesis that an increase in cell volume resulting from amino acid uptake may be involved in the stimulation of glycogen synthesis is supported by the following

  20. Novel Green Synthesis and Characterization of Nanopolymer ...

    African Journals Online (AJOL)

    Purpose: To develop a novel approach to green synthesis of nano-polymer porous gold oxide nanoparticles, and examine the effects of the temperatures on their surface. Methods: Green synthesis of nano-polymer porous gold oxide nanoparticles (GONPs) using cetyle trimethylammonium bromide (CTAB) surfactant with a ...

  1. Synthesis of graphene using gamma radiations

    Indian Academy of Sciences (India)

    Abstract. Considering the advantages of radiolytic synthesis such as the absence of toxic chemical as a reducing agent, uniform distribution of reducing agent and high purity of product, the synthesis of graphene (rGO) from graphene oxide (GO) by the gamma irradiation technique using a relatively low dose rate of 0.24 kGy ...

  2. Synthesis of graphene using gamma radiations

    Indian Academy of Sciences (India)

    Considering the advantages of radiolytic synthesis such as the absence of toxic chemical as a reducing agent, uniform distribution of reducing agent and high purity of product, the synthesis of graphene (rGO) from graphene oxide (GO) by the gamma irradiation technique using a relatively low dose rate of 0.24 kGy h−1 has ...

  3. Synthesis, spectroscopic characterization and electronic structure of ...

    Indian Academy of Sciences (India)

    Unknown

    Copper(I) carbene complex; carbene complex synthesis; Cu(I)–carbene electronic structure. 1. Introduction. Metal carbene complexes are arguably the most ver- satile organometallic reagents that have been devel- oped for organic synthesis.1 Different reactions of these complexes have been reported since their dis-.

  4. Sulfonated graphenes catalyzed synthesis of expanded porphyrins ...

    Indian Academy of Sciences (India)

    A newer synthesis of sulfonic acid functionalized graphenes have been developed, which have been characterized, examined as heterogeneous solid acid carbocatalyst in the synthesis of selected expanded porphyrins in different reaction conditions. This environment-friendly catalyst avoids the use of toxic catalysts and ...

  5. HMM Adaptation for child speech synthesis

    CSIR Research Space (South Africa)

    Govender, Avashna

    2015-09-01

    Full Text Available Hidden Markov Model (HMM)-based synthesis in combination with speaker adaptation has proven to be an approach that is well-suited for child speech synthesis. This paper describes the development and evaluation of different HMM-based child speech...

  6. Synthesis, characterization and application of semiconducting oxide ...

    Indian Academy of Sciences (India)

    Nanostructured; Cu2O nanostructures; electrolysis based oxidation; aligned ZnO nanorods. Abstract. In the present study, we report the synthesis, characterization and application of nanostructured oxide materials. The oxide ... The copper electrode served as a sacrificial anode for the synthesis of different nanostructures.

  7. Automatic Synthesis of Robust and Optimal Controllers

    DEFF Research Database (Denmark)

    Cassez, Franck; Jessen, Jan Jacob; Larsen, Kim Guldstrand

    2009-01-01

    In this paper, we show how to apply recent tools for the automatic synthesis of robust and near-optimal controllers for a real industrial case study. We show how to use three different classes of models and their supporting existing tools, Uppaal-TiGA for synthesis, phaver for verification...

  8. Synthesis of ammonia with microwave plasma

    International Nuclear Information System (INIS)

    Xu Wenguo; Yu Aimin; Liu Jun; Jin Qinhan

    1991-01-01

    THe synthesis of ammonia absorbed on 13X zeolite with the aid of microwave plasma is described. The ammonia molecule absorbed on 13X zeolite as ammonium ions were detected by IR spectroscopy. The results obtained show that the ammonia synthesis is facilitated by the surface reactions of NH x (x = 1, 2) radicals adsorbed on zeolite with hydrogen atoms

  9. Synthesis, Characterization and Antibacterial Activity of Imidazole ...

    African Journals Online (AJOL)

    NICO

    Synthesis, Characterization and Antibacterial Activity of. Imidazole Derivatives of 1,10-Phenanthroline and their .... Synthesis of Ligands (L1, L2). Ligands (L1. , L2) were synthesized by a method similar to one ... (50 mL). Dropwise addition of concentrated aqueaus ammonia to neutralize gave a yellow precipitate, which was ...

  10. Conceptual problems with remote element synthesis

    Indian Academy of Sciences (India)

    The notion of remote element synthesis has recently been modified to explain the presence of nucleogenetic isotopic anomalies and decay products of short-lived nuclides by injection of a small amount of exotic nucleogenetic material. Even with this modification, remote element synthesis seems inconsistent with the ...

  11. Standardized chemical synthesis of Pseudomonas aeruginosa pyocyanin

    Directory of Open Access Journals (Sweden)

    Rajkumar Cheluvappa

    2014-01-01

    As we have extracted pyocyanin both from P. aeruginosa cultures, and via chemical synthesis; we know the procedural and product-quality differences. We endorse the relative ease, safety, and convenience of using the chemical synthesis described here. Crucially, our “naturally endotoxin-free” pyocyanin can be extracted easily without using infectious bacteria.

  12. Heteropolyacids in synthesis of benzoyl hydrazone derivatives ...

    African Journals Online (AJOL)

    Keggin type of heteropolyacids as green reusable and efficient catalyst was used in the synthesis of benzoyl hydrazones from reaction of benzoic acid hydrazide and aldehyde and ketone derivatives. The synthesis of N-acetyl and N-benzoyl derivatives has also been performed by the reaction of obtained benzoyl ...

  13. MICROWAVE-ASSISTED SYNTHESIS OF SOME NITRO ...

    African Journals Online (AJOL)

    Chem. Life Sci. 2014, 347, 387-397. 32. Menteşe, E. Efficient microwave assisted synthesis of some new benzimidazoles containing the mebendazole nucleus. J. Chem. Res. 2013, 37, 168-170. 33. Menteşe, E.; Yılmaz, F.; Mutlu, F.; Kahveci, B. Synthesis of new coumarin containing benzimidazole derivatives. J. Chem. Res.

  14. Properties and synthesis of milrinone

    Directory of Open Access Journals (Sweden)

    Mirković Jelena M.

    2013-01-01

    Full Text Available Milrinone, 1,6-dihydro-2-methyl-6-oxo-[3,4’-bipyridine]-5-carbonitrile, is a positive inotropic cardiotonic agent with vasodilator properties that acts as selective phosphodiesterase 3 inhibitor in cardiac and vascular smooth muscle. Trade names of milrinone are Primacor, Corotrop, Corotrope, and Milrila. Milrinone, an amrinone derivative, is 20 to 50 times more active than amrinone and possesses reduced propensity to side effects. The use of milrinone has created controversy in the medical as the result of increased mortality rate among patients that received high amounts of milrinone in oral form. Reaserch show that it can be benifitial for patients with severe congestive heart failure when used as short-time intravenous therapy. Milrinone properties, stability, as well as mechanism of action and synthesis under laboratory and industry conditions have been described in this paper. For industrial purposes milrinone is synthesized by condensation of cyanoacetamide with 4-(dimethylamino-3-(4-pyridinyl-3-buten-2-one and 4-ethoxy-3-(4-pyridinyl-3-buten-2-one in presence of a base, or by the reaction of 1-(4-pyridinyl- 2-propanone with ethoxymethylenmalononitrile or 4-alkoxy-3-(4-pyridinyl-3-buten-2-one with malononitrile without the use of external base. The starting compound for these syntheses is 4-picoline. Alternative synthesis of milrinone starts from 2-methyl-3-(4-pyridylidiene-1,1,5-tricyano-1,4-pentadiene-5-carboxamide and 2-methyl-6-oxo-1,6-dihydro-3,4’-bipyridine-5-carboxamide. Lastly, methods for milrinone synthesis in laboratory, injection preparation and purification have been summarized.

  15. A Concise Synthesis of Forskolin.

    Science.gov (United States)

    Hylse, Ondřej; Maier, Lukáš; Kučera, Roman; Perečko, Tomáš; Svobodová, Aneta; Kubala, Lukáš; Paruch, Kamil; Švenda, Jakub

    2017-10-02

    A 24-step synthesis of (±)-forskolin is presented, which delivered hundred milligram quantities of this complex diterpene in one pass. Transformations key to our approach include: a) a strategic allylic transposition, b) stepwise assembly of a sterically encumbered isoxazole ring, and c) citric acid-modified Upjohn dihydroxylation of a resilient tetrasubstituted olefin. The developed route has exciting potential for the preparation of new forskolin analogues inaccessible by semisynthesis. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. Cellulose Synthesis in Agrobacterium tumefaciens

    Energy Technology Data Exchange (ETDEWEB)

    Alan R. White; Ann G. Matthysse

    2004-07-31

    We have cloned the celC gene and its homologue from E. coli, yhjM, in an expression vector and expressed the both genes in E. coli; we have determined that the YhjM protein is able to complement in vitro cellulose synthesis by extracts of A. tumefaciens celC mutants, we have purified the YhjM protein product and are currently examining its enzymatic activity; we have examined whole cell extracts of CelC and various other cellulose mutants and wild type bacteria for the presence of cellulose oligomers and cellulose; we have examined the ability of extracts of wild type and cellulose mutants including CelC to incorporate UDP-14C-glucose into cellulose and into water-soluble, ethanol-insoluble oligosaccharides; we have made mutants which synthesize greater amounts of cellulose than the wild type; and we have examined the role of cellulose in the formation of biofilms by A. tumefaciens. In addition we have examined the ability of a putative cellulose synthase gene from the tunicate Ciona savignyi to complement an A. tumefaciens celA mutant. The greatest difference between our knowledge of bacterial cellulose synthesis when we started this project and current knowledge is that in 1999 when we wrote the original grant very few bacteria were known to synthesize cellulose and genes involved in this synthesis were sequenced only from Acetobacter species, A. tumefaciens and Rhizobium leguminosarum. Currently many bacteria are known to synthesize cellulose and genes that may be involved have been sequenced from more than 10 species of bacteria. This additional information has raised the possibility of attempting to use genes from one bacterium to complement mutants in another bacterium. This will enable us to examine the question of which genes are responsible for the three dimensional structure of cellulose (since this differs among bacterial species) and also to examine the interactions between the various proteins required for cellulose synthesis. We have carried out one

  17. Synthesis document of the presentations

    International Nuclear Information System (INIS)

    Vrousos, C.; Choudat, D.; Dutrillaux, B.

    2001-01-01

    This colloquium has been organized to answer questions from health professionals. They are more and more confronted to public information about public health and to patient anxiety. The aim of the interventions is to realize a clearly and comprehensive synthesis of events concerning the nuclear and health domain during 2000. The following three sessions deal with this subject: occupational diseases and ionizing radiation; the public information and attitude facing nuclear accidents and especially Chernobyl; medical and sanitary aspects of a nuclear accident: management and follow up of people. (A.L.B.)

  18. Ibuprofen: Synthesis, production and properties

    Directory of Open Access Journals (Sweden)

    Mijin Dušan Ž.

    2003-01-01

    Full Text Available Since its introduction in 1969, ibuprofen has become one of the most common painkillers in the world. Ibuprofen in an NSAID (non-steroidal anti-inflammatory drug and like other drugs of its class it possesses analgetic, antipyretic and anti-inflammatory properties. While ibuprofen is a relatively simple molecule, there is still sufficient structural complexity to ensure that a large number of different synthetic approaches are possible. Since the introduction of pharmaceutical products containing ibuprofen, industrial and academic scientists have developed many potential production processes. This paper describes the history, synthesis and production, as well as the properties and stability of ibuprofen.

  19. Biological synthesis of silver nanoparticles

    International Nuclear Information System (INIS)

    Maliszewska, I; Szewczyk, K; Waszak, K

    2009-01-01

    Fungus-mediated synthesis of silver nanoparticles is reported. The nanosilver was formed in contact with the cell-free filtrate of Penicillium strain studied. The nanoparticles were characterized by means of the UV-Vis spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The synthesized nanosilver showed a absorbed maximum at 425 nm in the visible region. The SEM characterization of the fungus cells treated with silver nitrite indicated that the protein might be responsible for the reduction of silver ions. Transmission electron microscopy (TEM) micrograph showed formation of silver nanoparticles in the range of 10-100 nm.

  20. EXOPOLYSACCHARIDES SYNTHESIS ON INDUSTRIAL WASTES

    Directory of Open Access Journals (Sweden)

    T.P.

    2016-04-01

    Full Text Available Data from the literature and our own studies on the synthesis of microbial exopolysaccharides on various industrial waste (food industry, agricultural sector, biodiesel production, etc. are reviewed here. Utilization of industrial waste to obtain exopolysaccharides will solve not only the problem of secondary raw materials accumulation, but also will reduce the costs of the biosynthesis of practically valuable metabolites. In addition, some kinds of waste have a number of advantages compared to traditional carbohydrate substrates: aside from environmental health benefits, there are technological ones, like the presence of growth factors. There is also no need to use anti-foam substances and substrate sterilization in the latter case.

  1. The synthesis paradigm in genetics.

    Science.gov (United States)

    Rice, William R

    2014-02-01

    Experimental genetics with model organisms and mathematically explicit genetic theory are generally considered to be the major paradigms by which progress in genetics is achieved. Here I argue that this view is incomplete and that pivotal advances in genetics--and other fields of biology--are also made by synthesizing disparate threads of extant information rather than generating new information from experiments or formal theory. Because of the explosive expansion of information in numerous "-omics" data banks, and the fragmentation of genetics into numerous subdisciplines, the importance of the synthesis paradigm will likely expand with time.

  2. Computer Music Synthesis and Composition

    Science.gov (United States)

    Ayers, Lydia

    What is computer music composition? Composers are using the computer for everything from MIDI instruments communicating with computer sequencers, pitch trackers analyzing the sounds of acoustic instruments and converting them to pitch information, live performers with recorded music, performers with interactive computer programs, computer music produced by dancers using sensors, automatic music composition with the computer programs composing the music, composing with sounds or parts of sounds rather than notes, how to structure the use of time, composing with timbres, or the colors of sounds, and timbre morphing, such as a gong morphing to a voice, composing with textures and texture morphing, such as fluttertonguing morphing to pitch, granular synthesis, trills and convolution.

  3. Total Synthesis of Calophyline A.

    Science.gov (United States)

    Li, Guang; Xie, Xiaoni; Zu, Liansuo

    2016-08-22

    Reported herein is the total synthesis of calophyline A, an indoline natural product possessing distinct ring connectivity which has not been synthesized previously. The synthetic route features several key transformations, including an aza-pinacol rearrangement to construct the nitrogen-containing bridged [3.2.2] bicycle, a Heck cyclization to assemble the fused 6/5/6/5 ring system, and a challenging late-stage aldol reaction to generate both a neopentyl quaternary stereogenic center and an oxygen-containing bridged [3.2.1] bicycle. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  4. Synthesis of colloidal silica dumbbells.

    Science.gov (United States)

    Johnson, Patrick M; van Kats, Carlos M; van Blaaderen, Alfons

    2005-11-22

    We describe the synthesis and characterization of stable suspensions of monodisperse fluorescently labeled silica dumbbell particles. Pure dispersions of silica dumbbells with center-to-center lengths from 174 nm to 2.3 microm were produced with a variety of aspect ratios. Individual particles in concentrated dispersions of these particles could be imaged with confocal microscopy. These particles can be used as a colloidal model system for addressing fundamental questions about crystal and glass formation of low-aspect-ratio anisotropic particles. They also have potential in photonic applications and electro-optical devices.

  5. Synthesis of Ru alkylidene complexes

    Directory of Open Access Journals (Sweden)

    Renat Kadyrov

    2011-01-01

    Full Text Available The present work describes the robust synthesis of Ru alkylidene complexes (PCy32Cl2Ru=CHR – precursors for metathesis catalysts. Moreover, the dynamic behavior of complexes where R = 2-naphthyl and 2-thienyl was studied. 1H NMR techniques were employed to establish the preferred conformations in solution for both complexes and the energy barrier for rotation around single (Ru=CH–C(thienyl bond was estimated (ΔG≠303K = 12.6 kcal/mol.

  6. Ammonia synthesis at low temperatures

    DEFF Research Database (Denmark)

    Rod, Thomas Holm; Logadottir, Ashildur; Nørskov, Jens Kehlet

    2000-01-01

    Density functional theory (DFT) calculations of reaction paths and energies for the industrial and the biological catalytic ammonia synthesis processes are compared. The industrial catalyst is modeled by a ruthenium surface, while the active part of the enzyme is modeled by a MoFe6S9 complex...... have been carried out to evaluate its feasibility. The calculations suggest that it might be possible to catalytically produce ammonia from molecular nitrogen at low temperatures and pressures, in particular if energy is fed into the process electrochemically. (C) 2000 American Institute of Physics....

  7. Organic synthesis with stable isotopes

    International Nuclear Information System (INIS)

    Daub, G.H.; Kerr, V.N.; Williams, D.L.; Whaley, T.W.

    1978-01-01

    Some general considerations concerning organic synthesis with stable isotopes are presented. Illustrative examples are described and discussed. The examples include DL-2-amino-3-methyl- 13 C-butanoic-3,4- 13 C 2 acid (DL-valine- 13 C 3 ); methyl oleate-1- 13 C; thymine-2,6- 13 C 2 ; 2-aminoethanesulfonic- 13 C acid (taurine- 13 C); D-glucose-6- 13 C; DL-2-amino-3-methylpentanoic-3,4- 13 C 2 acid (DL-isoleucine- 13 C 2 ); benzidine- 15 N 2 ; and 4-ethylsulfonyl-1-naphthalene-sulfonamide- 15 N

  8. Synthesis of nanoparticles and nanomaterials biological approaches

    CERN Document Server

    Abdullaeva, Zhypargul

    2017-01-01

    This book covers biological synthesis approaches for nanomaterials and nanoparticles, including introductory material on their structure, phase compositions and morphology, nanomaterials chemical, physical, and biological properties. The chapters of this book describe in sequence the synthesis of various nanoparticles by microorganisms, bacteria, yeast, algae, and actynomycetes; plant and plant extract-based synthesis; and green synthesis methods. Each chapter provides basic knowledge on the synthesis of nanomaterials, defines fundamental terms, and aims to build a solid foundation of knowledge, followed by explanations, examples, visual photographs, schemes, tables and illustrations. Each chapter also contains control questions, problem drills, as well as case studies that clarify theory and the explanations given in the text. This book is ideal for researchers and advanced graduate students in materials engineering, biotechnology, and nanotechnology fields. As a reference book this work is also appropriate ...

  9. Protein chemical synthesis in drug discovery.

    Science.gov (United States)

    Liu, Fa; Mayer, John P

    2015-01-01

    The discovery of novel therapeutics to combat human disease has traditionally been among the most important goals of research chemists. After a century of innovation, state-of-the-art chemical protein synthesis is now capable of efficiently assembling proteins of up to several hundred residues in length from individual amino acids. By virtue of its unique ability to incorporate non-native structural elements, chemical protein synthesis has been seminal in the recent development of several novel drug discovery technologies. In this chapter, we review the key advances in peptide and protein chemistry which have enabled our current synthetic capabilities. We also discuss the synthesis of D-proteins and their applications in mirror image phage-display and racemic protein crystallography, the synthesis of enzymes for structure-based drug discovery, and the direct synthesis of homogenous protein pharmaceuticals.

  10. Feature-aware natural texture synthesis

    KAUST Repository

    Wu, Fuzhang

    2014-12-04

    This article presents a framework for natural texture synthesis and processing. This framework is motivated by the observation that given examples captured in natural scene, texture synthesis addresses a critical problem, namely, that synthesis quality can be affected adversely if the texture elements in an example display spatially varied patterns, such as perspective distortion, the composition of different sub-textures, and variations in global color pattern as a result of complex illumination. This issue is common in natural textures and is a fundamental challenge for previously developed methods. Thus, we address it from a feature point of view and propose a feature-aware approach to synthesize natural textures. The synthesis process is guided by a feature map that represents the visual characteristics of the input texture. Moreover, we present a novel adaptive initialization algorithm that can effectively avoid the repeat and verbatim copying artifacts. Our approach improves texture synthesis in many images that cannot be handled effectively with traditional technologies.

  11. Synthesis in the liquid phase

    Energy Technology Data Exchange (ETDEWEB)

    1943-03-11

    Justification is presented for an I.G. Farben patent on synthesis of hydrocarbons from carbon monoxide and hydrogen in the liquid phase. Tracing the history of the process, the report notes that Pier worked out the basic patent in 1928. Duftschmid of Farben/Oppau subsequently worked out a variation of the process using for the fluid medium a synthesis product consisting mainly of products vaporizing in the reaction. The process used fixed-bed catalysts. Ruhrchemie A.G. objected to this patent on grounds that the process was already known. Meanwhile, Michael of Farben/Ludwigshafen devised another variation using mainly a finely distributed sintered catalyst and very fast stirring. The process required a high boiling, practically non-volatile liquid phase to keep the finely distributed catalyst in motion in the liquid during the reaction. A good distribution of carbon monoxide, hydrogen, and catalyst was obtained by having the gases enter either through a filter plate or by a rapid stirring of the liquid. The report concludes that since Michael's process was not for fixed catalysts, it was in no way dependent on the Duftschmid process or on Oppau's patent rights. A detailed chronology of work on the processes is included.

  12. Homeobox genes and melatonin synthesis

    DEFF Research Database (Denmark)

    Rohde, Kristian; Møller, Morten; Rath, Martin Fredensborg

    2014-01-01

    Nocturnal synthesis of melatonin in the pineal gland is controlled by a circadian rhythm in arylalkylamine N-acetyltransferase (AANAT) enzyme activity. In the rodent, Aanat gene expression displays a marked circadian rhythm; release of norepinephrine in the gland at night causes a cAMP-based indu......Nocturnal synthesis of melatonin in the pineal gland is controlled by a circadian rhythm in arylalkylamine N-acetyltransferase (AANAT) enzyme activity. In the rodent, Aanat gene expression displays a marked circadian rhythm; release of norepinephrine in the gland at night causes a c......AMP-based induction of Aanat transcription. However, additional transcriptional control mechanisms exist. Homeobox genes, which are generally known to encode transcription factors controlling developmental processes, are also expressed in the mature rodent pineal gland. Among these, the cone-rod homeobox (CRX......) transcription factor is believed to control pineal-specific Aanat expression. Based on recent advances in our understanding of Crx in the rodent pineal gland, we here suggest that homeobox genes play a role in adult pineal physiology both by ensuring pineal-specific Aanat expression and by facilitating c...

  13. Mixed Alcohol Synthesis Catalyst Screening

    Energy Technology Data Exchange (ETDEWEB)

    Gerber, Mark A.; White, James F.; Stevens, Don J.

    2007-09-03

    National Renewable Energy Laboratory (NREL) and Pacific Northwest National Laboratory (PNNL) are conducting research to investigate the feasibility of producing mixed alcohols from biomass-derived synthesis gas (syngas). PNNL is tasked with obtaining commercially available or preparing promising mixed-alcohol catalysts and screening them in a laboratory-scale reactor system. Commercially available catalysts and the most promising experimental catalysts are provided to NREL for testing using a slipstream from a pilot-scale biomass gasifier. From the standpoint of producing C2+ alcohols as the major product, it appears that the rhodium catalyst is the best choice in terms of both selectivity and space-time yield (STY). However, unless the rhodium catalyst can be improved to provide minimally acceptable STYs for commercial operation, mixed alcohol synthesis will involve significant production of other liquid coproducts. The modified Fischer-Tropsch catalyst shows the most promise for providing both an acceptable selectivity to C2+ alcohols and total liquid STY. However, further optimization of the Fischer-Tropsch catalysts to improve selectivity to higher alcohols is highly desired. Selection of a preferred catalyst will likely entail a decision on the preferred coproduct slate. No other catalysts tested appear amenable to the significant improvements needed for acceptable STYs.

  14. Fluxnet Synthesis Dataset Collaboration Infrastructure

    Energy Technology Data Exchange (ETDEWEB)

    Agarwal, Deborah A. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Humphrey, Marty [Univ. of Virginia, Charlottesville, VA (United States); van Ingen, Catharine [Microsoft. San Francisco, CA (United States); Beekwilder, Norm [Univ. of Virginia, Charlottesville, VA (United States); Goode, Monte [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Jackson, Keith [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Rodriguez, Matt [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Weber, Robin [Univ. of California, Berkeley, CA (United States)

    2008-02-06

    The Fluxnet synthesis dataset originally compiled for the La Thuile workshop contained approximately 600 site years. Since the workshop, several additional site years have been added and the dataset now contains over 920 site years from over 240 sites. A data refresh update is expected to increase those numbers in the next few months. The ancillary data describing the sites continues to evolve as well. There are on the order of 120 site contacts and 60proposals have been approved to use thedata. These proposals involve around 120 researchers. The size and complexity of the dataset and collaboration has led to a new approach to providing access to the data and collaboration support and the support team attended the workshop and worked closely with the attendees and the Fluxnet project office to define the requirements for the support infrastructure. As a result of this effort, a new website (http://www.fluxdata.org) has been created to provide access to the Fluxnet synthesis dataset. This new web site is based on a scientific data server which enables browsing of the data on-line, data download, and version tracking. We leverage database and data analysis tools such as OLAP data cubes and web reports to enable browser and Excel pivot table access to the data.

  15. Clinical documentation: composition or synthesis?

    Science.gov (United States)

    Mamykina, Lena; Vawdrey, David K; Stetson, Peter D; Zheng, Kai; Hripcsak, George

    2012-01-01

    To understand the nature of emerging electronic documentation practices, disconnects between documentation workflows and computing systems designed to support them, and ways to improve the design of electronic documentation systems. Time-and-motion study of resident physicians' note-writing practices using a commercial electronic health record system that includes an electronic documentation module. The study was conducted in the general medicine unit of a large academic hospital. During the study, 96 note-writing sessions by 11 resident physicians, resulting in close to 100 h of observations were seen. Seven of the 10 most common transitions between activities during note composition were between documenting, and gathering and reviewing patient data, and updating the plan of care. The high frequency of transitions seen in the study suggested that clinical documentation is fundamentally a synthesis activity, in which clinicians review available patient data and summarize their impressions and judgments. At the same time, most electronic health record systems are optimized to support documentation as uninterrupted composition. This mismatch leads to fragmentation in clinical work, and results in inefficiencies and workarounds. In contrast, we propose that documentation can be best supported with tools that facilitate data exploration and search for relevant information, selective reading and annotation, and composition of a note as a temporal structure. Time-and-motion study of clinicians' electronic documentation practices revealed a high level of fragmentation of documentation activities and frequent task transitions. Treating documentation as synthesis rather than composition suggests new possibilities for supporting it more effectively with electronic systems.

  16. Abiogenic synthesis on terrestrial orbit

    Science.gov (United States)

    Simakov, Michael B.; Kuzicheva, Evgenia; Gontareva, Natalia

    Meteorites probably played a central role in the evolution of life. Due to the structure, they tend to adsorb organic compounds and catalyze a variety of organic reactions critical to scenarios of life’s origins. We have shown experimentally that extraterrestrial minerals can catalyze the formation of peptides and nucleotides. The present study was performed onboard different Russian space stations (BION, COSMOS, and MIR) with various duration, altitude, and radiation conditions. Irradiation of solid samples, free or admixed with certain minerals, was the major task of future space flight experiments, planned for performing onboard Russian space satellite Bion-M. The «simulated space ice conditions» experiments have shown the synthesis of simple biochemical compounds in the form of amino acid’s precursors and pyrimidine bases (uracil, cyrosine and thymine) of the nucleic acids. Our investigation dealt with further reaction of nucleic acid components to nucleotides - main components of RNA and DNA, and single aminoacids to oligopeptides. We investigated two types of reactions: (1) abiogenic synthesis of nucleotides from mixtures of nucleoside + inorganic phosphate; (2) abiogenic synthesis of dipeptides from mixtures of simple amino acids. The reaction mixture in the form of a solid film contains (1) nucleoside and dihydrogen phosphate; (2) two different amino acids. Seven different nucleosides (thymidine, cytidine, uracil, adenosine or deoxyadenosine, guanosine or deoxyguanosine) and four mixtures of aromatic (tyrosine or triptophan) and aliphatic (glycine or alanine) amino acids were investigated. Mixtures were irradiated as solid films with different sources of energy: (1) VUV-light of 145 nm; (2) high energy protons (2-6 MeV); and (3) were installed on the surface of biosputnik in outstanding container when they were exposed to the action of all spectra of the open space energy sources during the entire time of flight. We have shown experimentally that the

  17. Bioinspired synthesis of magnetic nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    David, Anand [Iowa State Univ., Ames, IA (United States)

    2009-01-01

    The synthesis of magnetic nanoparticles has long been an area of active research. Magnetic nanoparticles can be used in a wide variety of applications such as magnetic inks, magnetic memory devices, drug delivery, magnetic resonance imaging (MRI) contrast agents, and pathogen detection in foods. In applications such as MRI, particle uniformity is particularly crucial, as is the magnetic response of the particles. Uniform magnetic particles with good magnetic properties are therefore required. One particularly effective technique for synthesizing nanoparticles involves biomineralization, which is a naturally occurring process that can produce highly complex nanostructures. Also, the technique involves mild conditions (ambient temperature and close to neutral pH) that make this approach suitable for a wide variety of materials. The term 'bioinspired' is important because biomineralization research is inspired by the naturally occurring process, which occurs in certain microorganisms called 'magnetotactic bacteria'. Magnetotactic bacteria use biomineralization proteins to produce magnetite crystals having very good uniformity in size and morphology. The bacteria use these magnetic particles to navigate according to external magnetic fields. Because these bacteria synthesize high quality crystals, research has focused on imitating aspects of this biomineralization in vitro. In particular, a biomineralization iron-binding protein found in a certain species of magnetotactic bacteria, magnetospirillum magneticum, AMB-1, has been extracted and used for in vitro magnetite synthesis; Pluronic F127 gel was used to increase the viscosity of the reaction medium to better mimic the conditions in the bacteria. It was shown that the biomineralization protein mms6 was able to facilitate uniform magnetite synthesis. In addition, a similar biomineralization process using mms6 and a shorter version of this protein, C25, has been used to synthesize cobalt ferrite

  18. Method of production of ammonia synthesis gas

    Energy Technology Data Exchange (ETDEWEB)

    1943-09-10

    In the catalytic synthesis of complicated hydrocarbons from carbon monoxide and hydrogen at normal or slightly increased pressures by the Fischer--Tropsch process, or carried out at higher pressures in some other proposals, the synthesis gas was incompletely transformed. After the conclusion of the synthesis, the residual gas, upon the separation of the liquid constituents, contained, in addition to the unreacted carbon moxoxide and hydrogen, also considerable amounts of methane, carbon dioxide, and nitrogen from the original synthesis gas. This residual gas had been used as fuel. It was, however, pure and contained no sulfur or other catalyst poisons and burning it was considered uneconomical. It was proposed to make better use of it by using it as fuel. It was, however, pure and contained no sulfur or other catalyst poisons and burning it was considered uneconomical. It was proposed to make better use of it by using it as a raw material for the production of synthesis gas by decomposing the methane present in it with steam according to the equation CH/sub 4/ + H/sub 2/O = CO + 3H/sub 2/. This conversion was to be brought about either by a return to the producers or else in special splitting units. Also, it had been found that the residual gas, possibly even in the presence of oxygen compounds, could be conveniently used for the synthesis of ammonia. Several examples of ammonia synthesis were discussed.

  19. Synthesis of ammonia using sodium melt.

    Science.gov (United States)

    Kawamura, Fumio; Taniguchi, Takashi

    2017-09-14

    Research into inexpensive ammonia synthesis has increased recently because ammonia can be used as a hydrogen carrier or as a next generation fuel which does not emit CO 2 . Furthermore, improving the efficiency of ammonia synthesis is necessary, because current synthesis methods emit significant amounts of CO 2 . To achieve these goals, catalysts that can effectively reduce the synthesis temperature and pressure, relative to those required in the Haber-Bosch process, are required. Although several catalysts and novel ammonia synthesis methods have been developed previously, expensive materials or low conversion efficiency have prevented the displacement of the Haber-Bosch process. Herein, we present novel ammonia synthesis route using a Na-melt as a catalyst. Using this route, ammonia can be synthesized using a simple process in which H 2 -N 2 mixed gas passes through the Na-melt at 500-590 °C under atmospheric pressure. Nitrogen molecules dissociated by reaction with sodium then react with hydrogen, resulting in the formation of ammonia. Because of the high catalytic efficiency and low-cost of this molten-Na catalyst, it provides new opportunities for the inexpensive synthesis of ammonia and the utilization of ammonia as an energy carrier and next generation fuel.

  20. Exergy analysis of industrial ammonia synthesis

    International Nuclear Information System (INIS)

    Kirova-Yordanova, Zornitza

    2004-01-01

    Exergy consumption of ammonia production plants depends strongly on the ammonia synthesis loop design. Due to the thermodynamically limited low degree of conversion of hydrogen-nitrogen mixture to ammonia, industrial ammonia synthesis is implemented as recycle process (so-called 'ammonia synthesis loop'). Significant quantities of reactants are recycled back to reactor, after the removal of ammonia at low temperatures. Modern ammonia synthesis plants use well-developed heat- and cold recovery to improve the reaction heat utilisation and to reduce the refrigeration costs. In this work, the exergy method is applied to estimate the effect of the most important process parameters on the exergy efficiency of industrial ammonia synthesis. A specific approach, including suitable definitions of the system boundaries and process parameters, is proposed. Exergy efficiency indexes are discussed in order to make the results applicable to ammonia synthesis loops of various designs. The dependence of the exergy losses on properly selected independent process parameters is studied. Some results from detailed exergy analysis of the most commonly used ammonia synthesis loop design configurations at a wide range of selected parameters values are shown

  1. Drug Development of the Antimalarial Agent Artemisinin: Total Synthesis, Analog Synthesis, and Structure-Activity Relationship Studies

    Science.gov (United States)

    1990-08-15

    jHoluenesulfonyl hydrazide in tetrahydrofuran (THF), solvolysis of the ketal group and subsequent hydrazone formation was observed. Under base...ARTEMISININ: TOTAL SYNTHESIS , ANALOG SYNTHESIS , AND STRUCTURE-ACTIVITY RELATIONSHIP STUDIES mc Mitchell A. Avery, Ph.D. SRI International...Antimalarial Agent Artemisinin: Total Synthesis , Analog Synthesis and Structure-Activity Relationship Studies 12 PERSONAL AUTHOR(S) Mitchell A

  2. Synthesis and Characterization of Cluster-Derived Supported Bimetallic Catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Adams, Richard D; Amiridis, Michael D

    2008-10-10

    New procedures have been developed for synthesizing di- and tri-metallic cluster complexes. The chemical properties of the new complexes have been investigated, particularly toward the activation of molecular hydrogen. These complexes were then converted into bi- and tri-metallic nanoparticles on silica and alumina supports. These nanoparticles were characterized by electron microscopy and were then tested for their ability to produce catalytic hydrogenation of unsaturated hydrocarbons and for the preferential oxidation of CO in the presence of hydrogen. The bi- and tri-metallic nanoparticles exhibited far superior activity and selectivity as hydrogenation catalysts when compared to the individual metallic components. It was found that the addition of tin greatly improved the selectivity of the catalysts for the hydrogenation of polyolefins. The addition of iron improves the catalysts for the selective oxidation of CO by platinum in the presence of hydrogen. The observations should lead to the development of lower cost routes to molecules that can be used to produce polymers and plastics for use by the general public and for procedures to purify hydrogen for use as an alternative energy in the hydrogen economy of the future.

  3. Synthesis

    International Nuclear Information System (INIS)

    Voinis, Sylvie; Lalieux, Philippe; Thury, Marc; Horseman, Steve

    2001-01-01

    To prevent radioactive contamination and undue exposure to the public, it is required that long-lived and/or high-level radioactive wastes be isolated from the human environment for a very long period of time. For the purpose of isolating such wastes, the basic concept of deep disposal is to place packaged waste in a geological formation such as clay. One of main functions of the geological formation is to isolate waste from moving groundwater, thus minimising lixiviation of waste and advective radionuclide transport and, hence the amount of radionuclides that could reach the human environment. Improving our understanding of processes that might affect the containment properties of the geological barrier can reduce uncertainties about the performance of the repository. In particular, during the stepwise development of the research programme, it is important to clarify if fractures that might be induced by the excavation of the underground facilities might have a significant impact on the radiological safety of a repository in a host formation such as clay. In this framework, the self- healing properties of argillaceous media - often quoted as one of the advantages of such host formations - play a major role, notably in reducing the long-term impacts of such induced fracturing. Twenty-six participants representing several national waste management organisations, regulatory authorities, government agencies and the academic community from the OECD member countries and the EC took part in the Topical Session. The session was mainly aimed at exchanging information on: The general point of view on self-healing from geomechanical and geochemical experts; The approaches that are or will be followed by the various organisations in order to deal with the self-healing. The geological settings covered in the presentations related to the whole range of argillaceous media relevant to the disposal of radioactive wastes, including poorly indurated clays and indurated mud-stones, and shales. The purpose of these proceedings is to provide on the one hand a brief summary of the technical presentations and a record of the main conclusions and outcomes and, on the other hand, a compilation of the presentations' abstracts. very informative presentations provided an overview of the spectrum of the topic; such multidisciplinary overview was - to the knowledge of the Clay Club members - not available before the session; they demonstrated the necessity to consider self-healing in all types of argillaceous media considered as potential host formation; they illustrated the need to reconcile the geomechanical and the geochemical approaches vis-a-vis the self-healing. The discussions focused initially on the clarification of the two phrases 'self-healing' and 'self-sealing'

  4. Synthesis,

    Directory of Open Access Journals (Sweden)

    Ganesan Vanangamudi

    2017-02-01

    Full Text Available Twelve 2,5-dimethyl-3-thienyl chalcones [E-1-(2,5-dimethyl-3-thienyl-3-(substituted phenyl-2-propen-1-ones] have been synthesized by Claisen–Schmidt condensation of 3-acetyl-2,5-dimethyl furon and substituted benzaldehydes. Yields of the chalcones are more than 80%. These chalcones were characterized by their physical constants and spectral data. The group frequencies of infrared ν(cm−1 of CO s-cis and s-trans, CH in-plane and out of plane, CHCH out of plane, >CC< out of plane modes, NMR chemical shifts δ(ppm of Hα, Hβ, CO, Cα and Cβ of these chalcones were correlated with Hammett substituent constants, F and R parameters using single and multi-regression analyses. From the results of statistical analyses, the effects of substituents on the group frequencies are explained. Antibacterial, antifungal, antioxidant and insect antifeedant activities of these chalcones have been studied.

  5. Synthesis

    Directory of Open Access Journals (Sweden)

    Emel Pelit

    2016-05-01

    Full Text Available New optically active aminoalkylnaphthols were obtained by condensation of 2-naphthol, substituted aromatic and heteroaromatic aldehydes and (R-(+-1-phenylethylamine or (S-(−-1-phenylethylamine under conventional methods and ultrasonic irradiation. The enantiopure aminoalkylnaphthol derivatives were converted in ring-closure reaction with formaldehyde to the corresponding naphthoxazine derivatives.

  6. Synthesis of semiconductor polymers by inductive plasma

    International Nuclear Information System (INIS)

    Fernandez, G.; Cruz, G.; Olayo, M.G.; Morales, J.

    2003-01-01

    When carrying out the synthesis of semiconductor polymers by plasma it is important to consider the electric arrangement of the discharge since this it influences in the distribution of the energy of the particles in the reactor. The main electric arrangements in those that are developed the brightness discharges of radio frequency are resistive, capacitive and inductive. In the Laboratory of Materials processing by plasma of the ININ its have been worked different synthesis of polymers with resistive arrangements with good results. In this work the results of the synthesis and characterization of poly aniline and chlorate polyethylene by inductive plasma are presented. (Author)

  7. Sonochemical Synthesis of Cobalt Ferrite Nanoparticles

    Directory of Open Access Journals (Sweden)

    Partha P. Goswami

    2013-01-01

    Full Text Available Cobalt ferrite being a hard magnetic material with high coercivity and moderate magnetization has found wide-spread applications. In this paper, we have reported the sonochemical synthesis of cobalt ferrite nanoparticles using metal acetate precursors. The ferrite synthesis occurs in three steps (hydrolysis of acetates, oxidation of hydroxides, and in situ microcalcination of metal oxides that are facilitated by physical and chemical effects of cavitation bubbles. The physical and magnetic properties of the ferrite nano-particles thus synthesized have been found to be comparable with those reported in the literature using other synthesis techniques.

  8. Thermodynamics of carbothermic synthesis of actinide mononitrides

    International Nuclear Information System (INIS)

    Ogawa, T.; Shirasu, Y.; Minato, K.; Serizawa, H.

    1997-01-01

    Carbothermic synthesis will be further applied to the fabrication of nitride fuels containing minor actinides (MA) such as neptunium, americium and curium. A thorough understanding of the carbothermic synthesis of UN will be beneficial in the development of the MA-containing fuels. Thermodynamic analysis was carried out for conditions of practical interest in order to better understand the recent fabrication experiences. Two types of solution phases, oxynitride and carbonitride phases, were taken into account. The Pu-N-O ternary isotherm was assessed for the modelling of M(C, N, O). With the understanding of the UN synthesis, the fabrication problems of Am-containing nitrides are discussed. (orig.)

  9. Synthesis of plant hormones labelled by tritium

    International Nuclear Information System (INIS)

    Sidorov, G.V.; Myasoedov, N.F.

    1999-01-01

    Reaction of solid-phase catalytic hydrogenation, isotopic exchange with enriched tritium water, catalytic heterogenous isotopic exchange with gaseous tritium, hydrogenolysis as applied to synthesis of plants labelled by tritium were studied. Auxins, cytokinins, gibberellins, fusicoccins - representatives of the basic hormones of plants - were objects of investigations. In dependence on synthesis method compounds labelled by tritium were prepared with molar radioactivity from 5 up to 155 Ci/mmol. Order of universal approaches to synthesis of plant hormones labelled by tritium was formulated [ru

  10. Total synthesis of (±)-antroquinonol d.

    Science.gov (United States)

    Sulake, Rohidas S; Jiang, Yan-Feng; Lin, Hsiao-Han; Chen, Chinpiao

    2014-11-21

    Total synthesis of (±)-antroquinonol D, which is isolated from very expensive and rarely found Antrodia camphorata and which has potential anticancer properties, was achieved from 4-methoxyphenol. In addition, a Michael addition to dimethoxy cyclohexadienones was studied. The main step involved chelation and substrate-controlled diastereoselective reduction of cyclohexenone and lactonization. Lactone synthesis facilitated the diastereoselective reduction of ketone, which help control the desired stereochemistry at the crucial stereogenic center in the natural product. Other key reactions in the synthesis involved a Michael addition of dimethyl malonate on cyclohexadienone, dihydroxylation, and Wittig olefination. A sesquiterpene side chain was synthesized through coupling with geranyl phenyl sulfide and Bouveault-Blanc reduction.

  11. Convenient synthesis of deuterated aluminium hydrides

    Energy Technology Data Exchange (ETDEWEB)

    Pawelke, Roland H.; Felderhoff, Michael; Weidenthaler, Claudia [Max-Planck-Institut fuer Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Muelheim an der Ruhr (Germany); Schueth, Ferdi [Max-Planck-Institut fuer Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Muelheim an der Ruhr (Germany)], E-mail: schueth@mpi-muelheim.mpg.de

    2008-09-15

    We describe the ball-milling synthesis of alkali metal deuterides from commercial lithium aluminium deuteride. This reaction principle was exemplified by the mechanochemical synthesis of NaAlD{sub 4} and KAlD{sub 4}. NaAlD{sub 4} was prepared on the multi-gram scale by this procedure and purified by standard wet-chemical separation. Pure NaAlD{sub 4} was obtained and used for the synthesis of Ca(AlD{sub 4}){sub 2}. The formation of all products was verified by X-ray diffraction.

  12. Green chemistry oriented organic synthesis in water.

    Science.gov (United States)

    Simon, Marc-Olivier; Li, Chao-Jun

    2012-02-21

    The use of water as solvent features many benefits such as improving reactivities and selectivities, simplifying the workup procedures, enabling the recycling of the catalyst and allowing mild reaction conditions and protecting-group free synthesis in addition to being benign itself. In addition, exploring organic chemistry in water can lead to uncommon reactivities and selectivities complementing the organic chemists' synthetic toolbox in organic solvents. Studying chemistry in water also allows insight to be gained into Nature's way of chemical synthesis. However, using water as solvent is not always green. This tutorial review briefly discusses organic synthesis in water with a Green Chemistry perspective.

  13. Combinatorial synthesis of natural products

    DEFF Research Database (Denmark)

    Nielsen, John

    2002-01-01

    Combinatorial syntheses allow production of compound libraries in an expeditious and organized manner immediately applicable for high-throughput screening. Natural products possess a pedigree to justify quality and appreciation in drug discovery and development. Currently, we are seeing a rapid...... increase in application of natural products in combinatorial chemistry and vice versa. The therapeutic areas of infectious disease and oncology still dominate but many new areas are emerging. Several complex natural products have now been synthesised by solid-phase methods and have created the foundation...... for preparation of combinatorial libraries. In other examples, natural products or intermediates have served as building blocks or scaffolds in the synthesis of complex natural products, bioactive analogues or designed hybrid molecules. Finally, structural motifs from the biologically active parent molecule have...

  14. Synthesis and characterization of Taurine

    Directory of Open Access Journals (Sweden)

    B Bayarmaa

    2014-10-01

    Full Text Available Have been obtained 2-aminoethanesulfonic acid (taurine from ethanolamine, sulfuric acid and sodium sulfite during the synthesis in laboratory condition. The process involves two steps of reactions, the first was esterification of ethanolamine with sulfuric acid to produce the intermediate product of 2-aminoethyl ester which than was extended to the second step by sulfonation with sodium sulfite to produce 2-aminoethanesulfonic acid. Resulting product was analyzed using 1H-NMR, IR, FAB-MS analysis and examined purity characterizations of the synthesized products. DOI: http://dx.doi.org/10.5564/mjc.v14i0.200 Mongolian Journal of Chemistry 14 (40, 2013, p57-60

  15. Combustion synthesis continuous flow reactor

    Energy Technology Data Exchange (ETDEWEB)

    Maupin, G.D.; Chick, L.A.; Kurosky, R.P.

    1998-01-06

    The present invention is a reactor for combustion synthesis of inorganic powders. The reactor includes a reaction vessel having a length and a first end and a second end. The reaction vessel further has a solution inlet and a carrier gas inlet. The reactor further has a heater for heating both the solution and the carrier gas. In a preferred embodiment, the reaction vessel is heated and the solution is in contact with the heated reaction vessel. It is further preferred that the reaction vessel be cylindrical and that the carrier gas is introduced tangentially into the reaction vessel so that the solution flows helically along the interior wall of the reaction vessel. As the solution evaporates and combustion produces inorganic material powder, the carrier gas entrains the powder and carries it out of the reactor. 10 figs.

  16. Combustion synthesis continuous flow reactor

    Energy Technology Data Exchange (ETDEWEB)

    Maupin, Gary D. (Richland, WA); Chick, Lawrence A. (West Richland, WA); Kurosky, Randal P. (Maple Valley, WA)

    1998-01-01

    The present invention is a reactor for combustion synthesis of inorganic powders. The reactor includes a reaction vessel having a length and a first end and a second end. The reaction vessel further has a solution inlet and a carrier gas inlet. The reactor further has a heater for heating both the solution and the carrier gas. In a preferred embodiment, the reaction vessel is heated and the solution is in contact with the heated reaction vessel. It is further preferred that the reaction vessel be cylindrical and that the carrier gas is introduced tangentially into the reaction vessel so that the solution flows helically along the interior wall of the reaction vessel. As the solution evaporates and combustion produces inorganic material powder, the carrier gas entrains the powder and carries it out of the reactor.

  17. Electrochemical synthesis of multisegmented nanowires

    Energy Technology Data Exchange (ETDEWEB)

    Kok, Kuan-Ying; Ng, Inn-Khuan; Saidin, Nur Ubaidah [Malaysian Nuclear Agency, Bangi, 43000 Kajang (Malaysia)

    2012-11-27

    Electrochemical deposition has emerged as a promising route for nanostructure fabrication in recent years due to the many inherent advantages it possesses. This study focuses on the synthesis of high-aspect-ratio multisegmented Au/Ni nanowires using template-directed sequential electrochemical deposition techniques. By selectively removing the Ni segments in the nanowires, high-yield of pure gold nanorods of predetermined lengths was obtained. Alternatively, the sacrificial Ni segments in the nanowires can be galvanically displaced with Bi and Te to form barbells structures with Bi{sub x}Te{sub y} nanotubes attached to neighbouring gold segments. Detailed studies on the nanostructures obtained were carried out using various microscopy, diffraction and probebased techniques for structural, morphological and chemical characterizations.

  18. Total synthesis of mycalamide A.

    Science.gov (United States)

    Sohn, Jeong-Hun; Waizumi, Nobuaki; Zhong, H Marlon; Rawal, Viresh H

    2005-05-25

    This communication describes a concise and efficient total synthesis of mycalamide A by the convergent coupling of pederic acid unit with the mycalamine unit. The left-half, (+)-7-benzoylpederic acid, was synthesized from (2R,3R)-3-methylpent-4-en-2-ol in seven steps and 34.6% overall yield through a route that features a one-step Pd(II)-catalyzed tandem Wacker/Heck cyclization reaction to prepare the tetrahydropyran ring system. The right-half, the mycalamine unit, was synthesized in 21 steps and 10.5% overall yield from diethyl d-tartrate. Effective, stereoselective methods were developed for the assembly of the two parts to yield either mycalamide A or C(10)-epi-mycalamide A.

  19. Triboluminescence theory, synthesis, and application

    CERN Document Server

    Okoli, Okenwa; Fontenot, Ross; Hollerman, William

    2016-01-01

    This book expounds on progress made over the last 35 years in the theory, synthesis, and application of triboluminescence for creating smart structures. It presents in detail the research into utilization of the triboluminescent properties of certain crystals as new sensor systems for smart engineering structures, as well as triboluminescence-based sensor systems that have the potential to enable wireless, in-situ, real time and distributed (WIRD) structural health monitoring of composite structures. The sensor component of any structural health monitoring (SHM) technology — measures the effects of the external load/event and provides the necessary inputs for appropriate preventive/corrective action to be taken in a smart structure — sits at the heart of such a system. This volume explores advances in materials properties and structural behavior underlying creation of smart composite structures and sensor systems for structural health monitoring of critical engineering structures, such as bridges, aircraf...

  20. Fluid Mechanics Optimising Organic Synthesis

    Science.gov (United States)

    Leivadarou, Evgenia; Dalziel, Stuart

    2015-11-01

    The Vortex Fluidic Device (VFD) is a new ``green'' approach in the synthesis of organic chemicals with many industrial applications in biodiesel generation, cosmetics, protein folding and pharmaceutical production. The VFD is a rapidly rotating tube that can operate with a jet feeding drops of liquid reactants to the base of the tube. The aim of this project is to explain the fluid mechanics of the VFD that influence the rate of reactions. The reaction rate is intimately related to the intense shearing that promotes collision between reactant molecules. In the VFD, the highest shears are found at the bottom of the tube in the Rayleigh and the Ekman layer and at the walls in the Stewardson layers. As a step towards optimising the performance of the VFD we present experiments conducted in order to establish the minimum drop volume and maximum rotation rate for maximum axisymmetric spreading without fingering instability. PhD candidate, Department of Applied Mathematics and Theoretical Physics.

  1. Synthesis of B6 vitamin

    Directory of Open Access Journals (Sweden)

    Vučijak Nevena Ž.

    2009-01-01

    Full Text Available The importance of vitamin B6 has been known since its discovery in the 1940's. Chemical tests, elestrometric titration determinations, and absorption spectrum studies showed that this vitamin exists in three major chemical forms: pyridoxine (an alcohol, pyridoxal (an aldehyde, and pyridoxamine (a primary amine. Vitamin B6 is needed for more than 100 enzymes involved in protein metabolism, and it is assumed that this vitamin is cofactor of metabolic processes more important than any other substance. A deficiency of vitamin B6 in the human diet leads to severe disorders. Vitamin B6 is necessary for the proper function of the immune and nervous system, and helps the body convert protein to energy. This paper describes the history, properties and applications of vitamin B6, elucidation of chemical structure, and different procedures for synthesis of pyridoxine and pyridoxamine.

  2. Solution synthesis of germanium nanocrystals

    Science.gov (United States)

    Gerung, Henry [Albuquerque, NM; Boyle, Timothy J [Kensington, MD; Bunge, Scott D [Cuyahoga Falls, OH

    2009-09-22

    A method for providing a route for the synthesis of a Ge(0) nanometer-sized material from. A Ge(II) precursor is dissolved in a ligand heated to a temperature, generally between approximately 100.degree. C. and 400.degree. C., sufficient to thermally reduce the Ge(II) to Ge(0), where the ligand is a compound that can bond to the surface of the germanium nanomaterials to subsequently prevent agglomeration of the nanomaterials. The ligand encapsulates the surface of the Ge(0) material to prevent agglomeration. The resulting solution is cooled for handling, with the cooling characteristics useful in controlling the size and size distribution of the Ge(0) materials. The characteristics of the Ge(II) precursor determine whether the Ge(0) materials that result will be nanocrystals or nanowires.

  3. Silica Aerogel: Synthesis and Applications

    Directory of Open Access Journals (Sweden)

    Jyoti L. Gurav

    2010-01-01

    Full Text Available Silica aerogels have drawn a lot of interest both in science and technology because of their low bulk density (up to 95% of their volume is air, hydrophobicity, low thermal conductivity, high surface area, and optical transparency. Aerogels are synthesized from molecular precursors by sol-gel processing. Special drying techniques must be applied to replace the pore liquid with air while maintaining the solid network. Supercritical drying is most common; however, recently developed methods allow removal of the liquid at atmospheric pressure after chemical modification of the inner surface of the gels, leaving only a porous silica network filled with air. Therefore, by considering the surprising properties of aerogels, the present review addresses synthesis of silica aerogels by the sol-gel method, as well as drying techniques and applications in current industrial development and scientific research.

  4. Control synthesis of switched systems

    CERN Document Server

    Zhao, Xudong; Niu, Ben; Wu, Tingting

    2017-01-01

    This book offers its readers a detailed overview of the synthesis of switched systems, with a focus on switching stabilization and intelligent control. The problems investigated are not only previously unsolved theoretically but also of practical importance in many applications: voltage conversion, naval piloting and navigation and robotics, for example. The book considers general switched-system models and provides more efficient design methods to bring together theory and application more closely than was possible using classical methods. It also discusses several different classes of switched systems. For general switched linear systems and switched nonlinear systems comprising unstable subsystems, it introduces novel ideas such as invariant subspace theory and the time-scheduled Lyapunov function method of designing switching signals to stabilize the underlying systems. For some typical switched nonlinear systems affected by various complex dynamics, the book proposes novel design approaches based on inte...

  5. Synthesis gas method and apparatus

    Science.gov (United States)

    Kelly, Sean M.; Kromer, Brian R.; Litwin, Michael M.; Rosen, Lee J.; Christie, Gervase Maxwell; Wilson, Jamie R.; Kosowski, Lawrence W.; Robinson, Charles

    2013-01-08

    A method and apparatus for producing a synthesis gas product having one or more oxygen transport membrane elements thermally coupled to one or more catalytic reactors such that heat generated from the oxygen transport membrane element supplies endothermic heating requirements for steam methane reforming reactions occurring within the catalytic reactor through radiation and convention heat transfer. A hydrogen containing stream containing no more than 20 percent methane is combusted within the oxygen transport membrane element to produce the heat and a heated combustion product stream. The heated combustion product stream is combined with a reactant stream to form a combined stream that is subjected to the reforming within the catalytic reactor. The apparatus may include modules in which tubular membrane elements surround a central reactor tube.

  6. SPARSE FARADAY ROTATION MEASURE SYNTHESIS

    International Nuclear Information System (INIS)

    Andrecut, M.; Stil, J. M.; Taylor, A. R.

    2012-01-01

    Faraday rotation measure synthesis is a method for analyzing multichannel polarized radio emissions, and it has emerged as an important tool in the study of Galactic and extragalactic magnetic fields. The method requires the recovery of the Faraday dispersion function from measurements restricted to limited wavelength ranges, which is an ill-conditioned deconvolution problem. Here, we discuss a recovery method that assumes a sparse approximation of the Faraday dispersion function in an overcomplete dictionary of functions. We discuss the general case when both thin and thick components are included in the model, and we present the implementation of a greedy deconvolution algorithm. We illustrate the method with several numerical simulations that emphasize the effect of the covered range and sampling resolution in the Faraday depth space, and the effect of noise on the observed data.

  7. Synthesis of nanoparticles using ethanol

    Science.gov (United States)

    Wang, Jia Xu

    2017-01-24

    The present disclosure relates to methods for producing nanoparticles. The nanoparticles may be made using ethanol as the solvent and the reductant to fabricate noble-metal nanoparticles with a narrow particle size distributions, and to coat a thin metal shell on other metal cores. With or without carbon supports, particle size is controlled by fine-tuning the reduction power of ethanol, by adjusting the temperature, and by adding an alkaline solution during syntheses. The thickness of the added or coated metal shell can be varied easily from sub-monolayer to multiple layers in a seed-mediated growth process. The entire synthesis of designed core-shell catalysts can be completed using metal salts as the precursors with more than 98% yield; and, substantially no cleaning processes are necessary apart from simple rinsing. Accordingly, this method is considered to be a "green" chemistry method.

  8. Synthesis and characterization of tetraethylammonium tetrachloro ...

    Indian Academy of Sciences (India)

    Unknown

    Synthesis and characterization of tetraethylammonium tetrachloro- cobaltate crystals. M A KANDHASWAMY and V SRINIVASAN*. Department of Physics, Sri Ramakrishna Mission Vidyalaya College of Arts and Science, Coimbatore 641 020, India. MS received 7 February 2000; revised 27 December 2001. Abstract.

  9. Synthesis, Spectroscopic and Pharmacological Studies of Bivalent ...

    African Journals Online (AJOL)

    Synthesis, Spectroscopic and Pharmacological Studies of Bivalent Copper, Zinc and Mercury Complexes of Thiourea. ... All the metal complexes were characterized by elemental chemical analysis, molar conductance, magnetic susceptibility measurements and IR spectroscopy. Cu(II) complexes were additionally ...

  10. Biological synthesis and characterization of silver nanoparticles ...

    Indian Academy of Sciences (India)

    Biological synthesis and characterization of silver nanoparticles using. Eclipta alba leaf extract and evaluation of its cytotoxic and antimicrobial potential. PARAMASIVAM PREMASUDHA1, MUDILI VENKATARAMANA2,∗, MARRIAPPAN ABIRAMI3,. PERIYASAMY VANATHI4, KADIRVELU KRISHNA2 and RAMASAMY ...

  11. Iterative perceptual learning for social behavior synthesis

    NARCIS (Netherlands)

    de Kok, I.A.; Poppe, Ronald Walter; Heylen, Dirk K.J.

    We introduce Iterative Perceptual Learning (IPL), a novel approach to learn computational models for social behavior synthesis from corpora of human–human interactions. IPL combines perceptual evaluation with iterative model refinement. Human observers rate the appropriateness of synthesized

  12. Iterative Perceptual Learning for Social Behavior Synthesis

    NARCIS (Netherlands)

    de Kok, I.A.; Poppe, Ronald Walter; Heylen, Dirk K.J.

    We introduce Iterative Perceptual Learning (IPL), a novel approach for learning computational models for social behavior synthesis from corpora of human-human interactions. The IPL approach combines perceptual evaluation with iterative model refinement. Human observers rate the appropriateness of

  13. An introduction to statistical parametric speech synthesis

    Indian Academy of Sciences (India)

    - like models, has become competitive with established concatenative techniques over the last few years. This paper offers a non-mathematical introduction to this method of speech synthesis. It is intended to be complementary to the wide ...

  14. Synthesis of dehydrobenzoannulenes with pyrene core

    Indian Academy of Sciences (India)

    -diethynylpyrene and. 1,3,6,8-tetraethynylpyrene as building blocks is reported. A sequence involving Sonogashira coupling, Corey–. Fuchs reaction and oxidative coupling (Eglinton coupling) is used for the synthesis of pyrene-based dehy-.

  15. Combustion synthesis of bulk nanocrystalline iron alloys

    Directory of Open Access Journals (Sweden)

    Licai Fu

    2016-02-01

    Full Text Available The controlled synthesis of large-scale nanocrystalline metals and alloys with predefined architecture is in general a big challenge, and making full use of these materials in applications still requires greatly effort. The combustion synthesis technique has been successfully extended to prepare large-scale nanocrystalline metals and alloys, especially iron alloy, such as FeC, FeNi, FeCu, FeSi, FeB, FeAl, FeSiAl, FeSiB, and the microstructure can be designed. In this issue, recent progress on the synthesis of nanocrystalline metals and alloys prepared by combustion synthesis technique are reviewed. Then, the mechanical and tribological properties of these materials with microstructure control are discussed.

  16. Allyl functionalized phosphinite and phosphonite ligands: Synthesis ...

    Indian Academy of Sciences (India)

    Allyl functionalized phosphinite and phosphonite ligands: Synthesis, transition metal chemistry and orthopalladation reactions. SINGAPPAGUDEM GOVINDARAJUa, GUDDEKOPPA S ANANTHNAGa, SUSMITA NAIKa,. SHAIKH M MOBINb and MARAVANJI S BALAKRISHNAa,∗. aPhosphorus Laboratory, Department of ...

  17. FUNCTIONALIZED CALIXSPHERANDS - SYNTHESIS AND PEPTIDE COUPLING

    NARCIS (Netherlands)

    BAKKER, WII; HAAS, M; DENHERTOG, HJ; VERBOOM, W; DEZEEUW, D; BRUINS, AP; REINHOUDT, DN

    1994-01-01

    Calixspherands, like 1, form kinetically stable complexes with alkali metal cations. For practical in vivo applications coupling of these complexes with carrier molecules is mandatory, Therefore, a general method for the synthesis of functionalized calixspherand 17 was developed starting from

  18. Polymer nanotube nanocomposites: synthesis, properties, and applications

    National Research Council Canada - National Science Library

    Mittal, Vikas

    2010-01-01

    ... in these commercially important areas of polymer technology. It sums up recent advances in nanotube composite synthesis technology, provides basic introduction to polymer nanotubes nanocomposite technology for the readers new to this field, provides valuable...

  19. Synthesis of asymmetrical multiantennary human milk oligosaccharides

    NARCIS (Netherlands)

    Prudden, Anthony R; Liu, Lin; Capicciotti, Chantelle J.; Wolfert, Margreet A; Wang, Shuo; Gao, Zhongwei; Meng, Lu; Moremen, Kelley W; Boons, Geert-Jan

    2017-01-01

    Despite mammalian glycans typically having highly complex asymmetrical multiantennary architectures, chemical and chemoenzymatic synthesis has almost exclusively focused on the preparation of simpler symmetrical structures. This deficiency hampers investigations into the biology of glycan-binding

  20. Synthesis and biological activities of substituted N ...

    African Journals Online (AJOL)

    use

    2011-12-07

    Dec 7, 2011 ... The present study describes the synthesis, antioxidant and antibacterial activities of substituted N'- benzoylhydrazone derivatives, to ... addition, the dramatically rising prevalence of multidrug- resistant microbial infections has ...... extract of Chinese green tea (Camellia sinensis) on Listeria monocytogenes.

  1. Copper catalysed synthesis of indolylquinazolinone alkaloid ...

    Indian Academy of Sciences (India)

    We describe the total synthesis of indolylquinazolinone alkaloid bouchardatine and some of the quinazolinone derivatives. The aerobic oxidation induced by copper(I) bromide, followed by Vilsmeier-Haack formylation gives the natural product bouchardatine alkaloid in good yield.

  2. Non-covalent synthesis of organic nanostructures

    NARCIS (Netherlands)

    Prins, L.J.; Timmerman, P.; Reinhoudt, David

    1998-01-01

    This review describes the synthesis, characterization and functionalization of hydrogen bonded, box-like assemblies. These assemblies are formed upon mixing bismelamine calix[4]arenes with a complementary barbiturate in apolar solvents. Various techniques for the characterization have been used,

  3. SHORT COMMUNICATION CONVENIENT AND MILD SYNTHESIS ...

    African Journals Online (AJOL)

    Preferred Customer

    , Synthesis. INTRODUCTION. Schiff bases are reagents, which are becoming increasingly important in the pharmaceutical, dye and plastic industries as well as for liquid-crystal technology and mechanistic investigations of the drugs used in ...

  4. Synthesis algorithm of VLSI multipliers for ASIC

    Science.gov (United States)

    Chua, O. H.; Eldin, A. G.

    1993-01-01

    Multipliers are critical sub-blocks in ASIC design, especially for digital signal processing and communications applications. A flexible multiplier synthesis tool is developed which is capable of generating multiplier blocks for word size in the range of 4 to 256 bits. A comparison of existing multiplier algorithms is made in terms of speed, silicon area, and suitability for automated synthesis and verification of its VLSI implementation. The algorithm divides the range of supported word sizes into sub-ranges and provides each sub-range with a specific multiplier architecture for optimal speed and area. The algorithm of the synthesis tool and the multiplier architectures are presented. Circuit implementation and the automated synthesis methodology are discussed.

  5. Diagnosis, Synthesis and Analysis of Probabilistic Models

    NARCIS (Netherlands)

    Han, Tingting

    2009-01-01

    This dissertation considers three important aspects of model checking Markov models: diagnosis — generating counterexamples, synthesis — providing valid parameter values and analysis — verifying linear real-time properties. The three aspects are relatively independent while all contribute to

  6. Synthesis methodology and applied heterocyclic chemistry

    International Nuclear Information System (INIS)

    Suzenet, F.

    2007-11-01

    Among the researches activities presented in this work, is described the synthesis of extracting molecules for the reprocessing of nuclear wastes. The use of some elaborated ligands for the detection of metallic cations has been considered. (O.M.)

  7. Albumin synthesis in protein energy malnutrition

    International Nuclear Information System (INIS)

    Duggan, C.; Hardy, S.; Kleinman, R.E.; Lembcke, J.; Young, V.E.

    1994-01-01

    The dietary treatment of protein-energy malnutrition (PEM) has been designed on an empirical basis, with outcomes for successful management including body weight gain and resolution of apathy. We propose using the measurements of protein synthesis as a more objective measure of renourishment. We will therefore randomize a group of malnourished children (weigh-for-height Z score 13 C-leucine and serial measurements of 13 C-enrichment of albumin. Isotope infusions will be performed on days one and three, following a standard three hour fast. Since albumin synthesis is reduced under the influence of cytokines which mediate the inflammatory response, results will be stratified according to the presence or absence of clinically apparent infections. We hypothesize that the provision of added dietary protein will optimize albumin synthesis rates in PEM as well as attenuate the reduction in albumin synthesis seen in the presence of infections. (author). 20 refs

  8. Anthrax carbohydrates, synthesis and uses thereof

    Science.gov (United States)

    Carlson, Russell W.; Boons, Geert-Jan; Quinn, Conrad; Vasan, Mahalakshmi; Wolfert, Margreet A.; Choudhury, Biswa; Kannenberg, Elmar; Leoff, Christine; Mehta, Alok; Saile, Elke; Rauvolfova, Jana; Wilkins, Patricia; Harvey, Alex J.

    2013-04-16

    The present invention presents the isolation, characterization and synthesis of oligosaccharides of Bacillus anthracis. Also presented are antibodies that bind to such saccharide moieties and various methods of use for such saccharide moieties and antibodies.

  9. Solving fault diagnosis problems linear synthesis techniques

    CERN Document Server

    Varga, Andreas

    2017-01-01

    This book addresses fault detection and isolation topics from a computational perspective. Unlike most existing literature, it bridges the gap between the existing well-developed theoretical results and the realm of reliable computational synthesis procedures. The model-based approach to fault detection and diagnosis has been the subject of ongoing research for the past few decades. While the theoretical aspects of fault diagnosis on the basis of linear models are well understood, most of the computational methods proposed for the synthesis of fault detection and isolation filters are not satisfactory from a numerical standpoint. Several features make this book unique in the fault detection literature: Solution of standard synthesis problems in the most general setting, for both continuous- and discrete-time systems, regardless of whether they are proper or not; consequently, the proposed synthesis procedures can solve a specific problem whenever a solution exists Emphasis on the best numerical algorithms to ...

  10. Microwave chemistry for inorganic nanomaterials synthesis.

    Science.gov (United States)

    Bilecka, Idalia; Niederberger, Markus

    2010-08-01

    This Feature Article gives an overview of microwave-assisted liquid phase routes to inorganic nanomaterials. Whereas microwave chemistry is a well-established technique in organic synthesis, its use in inorganic nanomaterials' synthesis is still at the beginning and far away from having reached its full potential. However, the rapidly growing number of publications in this field suggests that microwave chemistry will play an outstanding role in the broad field of Nanoscience and Nanotechnology. This article is not meant to give an exhaustive overview of all nanomaterials synthesized by the microwave technique, but to discuss the new opportunities that arise as a result of the unique features of microwave chemistry. Principles, advantages and limitations of microwave chemistry are introduced, its application in the synthesis of different classes of functional nanomaterials is discussed, and finally expected benefits for nanomaterials' synthesis are elaborated.

  11. Synthesis of substituted 2-cyanoarylboronic esters

    DEFF Research Database (Denmark)

    Lysén, Morten; Hansen, Henriette M; Begtrup, Mikael

    2006-01-01

    The synthesis of substituted 2-cyanoarylboronic esters is described via lithiation/in situ trapping of the corresponding methoxy-, trifluoromethyl-, fluoro-, chloro-, and bromobenzonitriles. The crude arylboronic esters were obtained in high yields and purities and with good regioselectivities....

  12. Synthesis, mechanical, thermal and chemical properties of ...

    Indian Academy of Sciences (India)

    Unknown

    Synthesis, mechanical, thermal and chemical properties of polyurethanes based on cardanol. C V MYTHILI, A MALAR RETNA and S GOPALAKRISHNAN*. Department of Chemistry, Manonmaniam Sundaranar University, Abishekapatti, Tirunelveli 627 012, India. MS received 28 August 2003; revised 19 February 2004.

  13. Microbiological synthesis of methyl ethyl ketone

    Directory of Open Access Journals (Sweden)

    Astashkina Anna

    2016-01-01

    Full Text Available Optimal conditions for the microbiological synthesis of methyl ethyl ketone (MEK on the mineral medium with butanol-1, butanol-2, 2-methylpropanol-2 by hydrocarbon-oxidizing bacteria Pseudomonas spp. were chosen. Optimal conditions for microbiological synthesis are liquid mineral Adkins’ medium containing 3% (vol. of the substrate, stirring speed – 80-100 rev/min, temperature – 37° C, and synthesis time 24-48 hours. The specific growth rate and time of culture generation during the microbial synthesis were determined. It was found that methyl ethyl ketone is formed in the reaction mixture after 8, 48 and 72 hours when using 2-methylpropanol-2, butanol-2, butanol-1 as substrates, respectively. Maximum methyl ethyl ketone yield in the reaction mixture is observed after 12 hours in the case of using 2-methylpropanol-2 as a carbon source and accounts for 10%.

  14. Synthesis, characterization and ion exchange properties of ...

    Indian Academy of Sciences (India)

    –1 dry exchanger, respectively. The material ... been found to have better properties than the simple salts of metals. The selectivity may be enhanced ... capacity and higher stability at elevated temperature. This paper deals with the synthesis, ...

  15. Iridium catalysed synthesis of piperazines from diols

    DEFF Research Database (Denmark)

    Nordstrøm, Lars Ulrik Rubæk; Madsen, Robert

    2007-01-01

    A green and atom-economical method has been developed for the synthesis of piperazines by cyclocondensation of diols and amines in aqueous media in the presence of a catalytic amount of [Cp*IrCl2]2....

  16. Synthesis, antioxidant and antimicrobial evaluation of thiazolidinone ...

    Indian Academy of Sciences (India)

    Vol. 124, No. 2, March 2012, pp. 469–481. c Indian Academy of Sciences. Synthesis, antioxidant and antimicrobial evaluation of thiazolidinone, azetidinone encompassing indolylthienopyrimidines. ANAND RAGHUNATH SAUNDANE. ∗. , MANJUNATHA YARLAKATTI,. PRABHAKER WALMIK and VIJAYKUMAR KATKAR.

  17. Variational inference & deep learning : A new synthesis

    NARCIS (Netherlands)

    Kingma, D.P.

    2017-01-01

    In this thesis, Variational Inference and Deep Learning: A New Synthesis, we propose novel solutions to the problems of variational (Bayesian) inference, generative modeling, representation learning, semi-supervised learning, and stochastic optimization.

  18. Surface active monomers synthesis, properties, and application

    CERN Document Server

    Borzenkov, Mykola

    2014-01-01

    This brief includes information on the background?of and development of synthesis of various types of surface active monomers. The authors explain the importance of utilization of surface active monomers for creation of surface active polymers? and the various biomedical applications of such compounds . This brief introduces techniques for the synthesis of novel types of surface active monomers, their colloidal and polymerizable properties and application for needs of medicine and biology.

  19. Embedded System Synthesis under Memory Constraints

    DEFF Research Database (Denmark)

    Madsen, Jan; Bjørn-Jørgensen, Peter

    1999-01-01

    This paper presents a genetic algorithm to solve the system synthesis problem of mapping a time constrained single-rate system specification onto a given heterogeneous architecture which may contain irregular interconnection structures. The synthesis is performed under memory constraints, that is......, the algorithm takes into account the memory size of processors and the size of interface buffers of communication links, and in particular the complicated interplay of these. The presented algorithm is implemented as part of the LY-COS cosynthesis system....

  20. Synthesis of disk-on-rod antennas

    Science.gov (United States)

    Dubrovka, F. F.; Lenivenko, V. A.

    1993-05-01

    The analysis and synthesis of disk-on-rod antennas (DORAs) with canonical and stepwise disk shapes are considered. A comparison of theoretical and experimental results shows that mathematical models and software developed by solving the appropriate boundary value problems can be used for the design of optimal DORAs. A broadband centimeter-wave DORA is considered as an example of the application of the proposed method for the constructive synthesis of DORAs using multicriterial optimization.

  1. Protein synthesis in the growing rat lung

    International Nuclear Information System (INIS)

    Kelley, J.; Chrin, L.

    1986-01-01

    Developmental control of protein synthesis in the postnatal growth of the lung has not been systematically studied. In male Fischer 344 rats, lung growth continues linearly as a function of body weight (from 75 to 450 g body weight). To study total protein synthesis in lungs of growing rats, we used the technique of constant intravenous infusion of tritiated leucine, an essential amino acid. Lungs of sacrificed animals were used to determine the leucine incorporation rate into newly synthesized protein. The specific radioactivity of the leucine associated with tRNA extracted from the same lungs served as an absolute index of the precursor leucine pool used for lung protein synthesis. On the basis of these measurements, we were able to calculate the fractional synthesis rate (the proportion of total protein destroyed and replaced each day) of pulmonary proteins for each rat. Under the conditions of isotope infusion, leucyl-tRNA very rapidly equilibrates with free leucine of the plasma and of the extracellular space of the lung. Infusions lasting 30 minutes or less yielded linear rates of protein synthesis without evidence of contamination of lung proteins by newly labeled intravascular albumin. The fractional synthesis rate is considerably higher in juvenile animals (55% per day) than in adult rats (20% per day). After approximately 12 weeks of age, the fractional synthesis rate remains extremely constant in spite of continued slow growth of the lung. It is apparent from these data that in both young and adult rats the bulk of total protein synthesis is devoted to rapidly turning over proteins and that less than 4 percent of newly made protein is committed to tissue growth

  2. Organosilicon and organogermanium peroxides: synthesis and reactions

    International Nuclear Information System (INIS)

    Terent'ev, Alexander O; Platonov, Maksim M; Levitsky, D O; Dembitsky, V M

    2011-01-01

    The methods of synthesis and reactions of organosilicon and organogermanium peroxides are surveyed. The emphasis is placed on the studies reported in the last two decades, because in this period, the use of singlet oxygen and the Isayama–Mukaiyama reaction for the synthesis of organosilicon peroxides started. The use of these compounds in the development of antiparasitic agents is considered. The bibliography includes 220 references.

  3. Hypoxia. 3. Hypoxia and neurotransmitter synthesis

    OpenAIRE

    Kumar, Ganesh K.

    2011-01-01

    Central and peripheral neurons as well as neuroendocrine cells express a variety of neurotransmitters/modulators that play critical roles in regulation of physiological systems. The synthesis of several neurotransmitters/modulators is regulated by O2-requiring rate-limiting enzymes. Consequently, hypoxia resulting from perturbations in O2 homeostasis can affect neuronal functions by altering neurotransmitter synthesis. Two broad categories of hypoxia are frequently encountered: continuous hyp...

  4. ANALYTICAL SYNTHESIS OF CHEMICAL REACTOR CONTROL SYSTEM

    Directory of Open Access Journals (Sweden)

    Alexander Labutin

    2017-02-01

    Full Text Available The problem of the analytical synthesis of the synergetic control system of chemical reactor for the realization of a complex series-parallel exothermal reaction has been solved. The synthesis of control principles is performed using the analytical design method of aggregated regulators. Synthesized nonlinear control system solves the problem of stabilization of the concentration of target component at the exit of reactor and also enables one to automatically transfer to new production using the equipment.

  5. Synthesis of Polyfunctionalized 4H-Pyrans

    Directory of Open Access Journals (Sweden)

    Manisha Bihani

    2013-01-01

    Full Text Available Amberlyst A21 catalyzed one-pot three-component coupling of aldehyde and malononitrile with active methylene compounds such as acetylacetone and ethyl acetoacetate for the synthesis of pharmaceutically important polyfunctionalized 4H-pyrans has been reported. Simple experimental procedure, no chromatographic purification, no hazardous organic solvents, easy recovery and reusability of the catalyst, and room temperature reaction conditions are some of the highlights of this protocol for the synthesis of pharmaceutically relevant focused libraries.

  6. An improved pattern synthesis algorithm based on metric modes

    Science.gov (United States)

    Tan, Yongqian; Zeng, Fanju; Zhang, Song; Yang, Yongliang

    2017-08-01

    Based on the principle of texture image synthesis of block splicing, the application of texture synthesis algorithm in pattern synthesis is studied. Through the study of the characteristics of texture image and texture pattern, it is found that texture is a special image with both localization and stability, and the pattern is a kind of whole structure with stronger structure. Texture synthesis algorithm in the more texture image synthesis, can achieve a more satisfactory results, but the synthesis of the pattern cannot achieve better synthesis results. In this paper, through the study of the characteristics of the pattern, on the basis of the texture synthesis algorithm, by improving the measurement method, when judging the similarity of two matching blocks, while the color and gradient of the image block as the two matching blocks are similar between the important parameters. Experiments show that the improved algorithm can achieve better synthesis effect when synthesizing most of the patterns.

  7. Histidine as a catalyst in organic synthesis: A facile in situ synthesis ...

    Indian Academy of Sciences (India)

    Unknown

    Nitrones are versatile synthetic intermediates in organic synthesis 1–8. Some nitrones are used for trapping and identification of reactive free radicals 9, particularly in biomedical research 10. They are also used in the synthesis of many nitrogen-containing biologically active compounds 11,12. Recently, we synthesized ...

  8. Biocatalyzed Regioselective Synthesis in Undergraduate Organic Laboratories: Multistep Synthesis of 2-Arachidonoylglycerol

    Science.gov (United States)

    Johnston, Meghan R.; Makriyannis, Alexandros; Whitten, Kyle M.; Drew, Olivia C.; Best, Fiona A.

    2016-01-01

    In order to introduce the concepts of biocatalysis and its utility in synthesis to organic chemistry students, a multistep synthesis of endogenous cannabinergic ligand 2-arachidonoylglycerol (2-AG) was tailored for use as a laboratory exercise. Over four weeks, students successfully produced 2-AG, purifying and characterizing products at each…

  9. Histidine as a catalyst in organic synthesis: A facile in situ synthesis ...

    Indian Academy of Sciences (India)

    Home; Journals; Journal of Chemical Sciences; Volume 113; Issue 4. Histidine as a catalyst in organic synthesis: A facile in situ synthesis of , N-diarylnitrones. H Mallesha K R Ravi Kumar B K Vishu Kumar K Mantelingu K S Rangappa. Organic Volume 113 Issue 4 August 2001 pp 291-296 ...

  10. Synthesis of polyaryl rigid-core carbosilane dendrimers for supported organic synthesis

    NARCIS (Netherlands)

    Wander, M.; Hausoul, P.J.C.; Sliedregt, L.A.J.M.; van Steen, B.J.; van Koten, G.; Klein Gebbink, R.J.M.

    2009-01-01

    Carbosilane dendrimers can be used as soluble supports for organic synthesis, since their structure allows separation of excess reagents from the supported products, eventually yielding products of high purity and in high yield, as in solid-phase organic synthesis (SPOS). In previous studies often

  11. Synthesis of derivatives of tetronic acid and pulvinic acid. Total synthesis of norbadione A

    International Nuclear Information System (INIS)

    Mallinger, A.

    2008-11-01

    When vegetables like mushrooms are contaminated by radioactive caesium 137, this radioactive caesium is associated to norbadione A, a natural pigment present in two mushroom species and which can be used as a caesium decorporation agent or maybe as protection agent against ionizing radiations. Within this perspective, this research report describes the biosynthesis and the structure and properties of the norbadione A and of pulvinic acids (physicochemical properties, anti-oxidizing properties). Then, it presents the various tetronic acids (3-acyl-, 3-alkyl-, 3-alkoxy-, 3-aryl-tetronic acids and non 3-substituted tetronic acids), their synthesis path as they are described in the literature, and presents a new synthesis approach using a tandem reaction (with different esters or hydroxy esters) and the synthesis of tetronic acids. The author also proposes a new synthesis way for methyl pulvinates, and finally reports the work on the development of a total synthesis of the norbadione A

  12. Effect of hemodialysis on protein synthesis.

    Science.gov (United States)

    Löfberg, E; Essén, P; McNurlan, M; Wernerman, J; Garlick, P; Anderstam, B; Bergström, J; Alvestrand, A

    2000-10-01

    Earlier studies have shown that hemodialysis (HD) treatment stimulates net protein catabolism. Several factors associated with HD affect protein catabolism, such as an inflammatory effect due to blood-membrane contact and loss of amino acids and glucose into the dialysate. We have studied protein synthesis in skeletal muscle of healthy volunteers (n = 9) before and after a single heparin-free HD. Protein synthesis (PS) was studied, using 2 independent techniques: the incorporation of labeled 2H5-phenylalanine into muscle protein, which gives a quantitative measure of the fractional synthesis rate of muscle proteins, and the concentration and size distribution of ribosomes, which gives a qualitative estimate of protein synthesis. Furthermore, free amino acid concentrations were determined in muscle and plasma. The rate of PS, expressed as the fractional synthesis rate, decreased by 13% during HD (p muscle free amino acid concentrations were determined at four time points; before and after the phenylalanine incorporation period, before dialysis and before and after the second incorporation period after dialysis. Immediately after dialysis, there was a decrease in plasma asparagine, histidine, alanine, taurine, valine and tryptophane. In muscle, no changes occurred except for a slight increase in leucine after dialysis. In blood, the glucose concentration decreased and the total amount of glucose lost to the dialysate was 21 +/- 3.0 g. In summary, one single hemodialysis treatment decreases fractional protein synthesis rate in skeletal muscle. The results demonstrate substantial losses of amino acids and glucose to the dialysate and decreased amino acid concentrations in plasma, but only minimal changes in the intracellular amino acid concentrations in muscle, suggesting that the decreased PS is caused not by lack of amino acid precursors at the site of the synthesis activity, but by other mechanisms.

  13. Sustainable processes synthesis for renewable resources

    International Nuclear Information System (INIS)

    Halasz, L.; Povoden, G.; Narodoslawsky, M.

    2005-01-01

    Renewable resources pose special challenges to process synthesis. Due to decentral raw material generation, usually low transport densities and the perishable character of most renewable raw materials in combination with their time dependent availability, logistical questions as well as adaptation to regional agricultural structures are necessary. This calls for synthesis of structures not only of single processes but of the whole value chain attached to the utilisation of a certain resource. As most of the innovative technologies proposed to build on a renewable raw material base face stiff economic competition from fossil based processes, economic optimality of the value chain is crucial to their implementation. On top of this widening of the process definition for synthesis, many processes on the base of renewable resources apply technologies (like membrane separations, chromatographic purification steps, etc.) for which the heuristic knowledge is still slim. This reduces the choice of methods for process synthesis, mainly to methods based on combinatorial principles. The paper investigates applicability as well as impact on technology development of process synthesis for renewable raw material utilisation. It takes logistic considerations into account and applies process synthesis to the case study of the green biorefinery concept. The results show the great potential of process synthesis for technology development of renewable resource utilisation. Applied early in the development phase, it can point towards the most promising utilisation pathways, thus guiding the engineering work. On top of that, and even more important, it can help avoid costly development flops as it also clearly indicates 'blind alleys' that have to be avoided

  14. Ammonia Synthesis at Low Pressure.

    Science.gov (United States)

    Cussler, Edward; McCormick, Alon; Reese, Michael; Malmali, Mahdi

    2017-08-23

    Ammonia can be synthesized at low pressure by the use of an ammonia selective absorbent. The process can be driven with wind energy, available locally in areas requiring ammonia for synthetic fertilizer. Such wind energy is often called "stranded," because it is only available far from population centers where it can be directly used. In the proposed low pressure process, nitrogen is made from air using pressure swing absorption, and hydrogen is produced by electrolysis of water. While these gases can react at approximately 400 °C in the presence of a promoted conventional catalyst, the conversion is often limited by the reverse reaction, which makes this reaction only feasible at high pressures. This limitation can be removed by absorption on an ammine-like calcium or magnesium chloride. Such alkaline metal halides can effectively remove ammonia, thus suppressing the equilibrium constraints of the reaction. In the proposed absorption-enhanced ammonia synthesis process, the rate of reaction may then be controlled not by the chemical kinetics nor the absorption rates, but by the rate of the recycle of unreacted gases. The results compare favorably with ammonia made from a conventional small scale Haber-Bosch process.

  15. Mechanochemical synthesis of bismuth ferrite

    Directory of Open Access Journals (Sweden)

    Marinković-Stanojevića Z.

    2013-01-01

    Full Text Available A powder mixture of Bi2O3 and Fe2O3 was mechanically treated in a planetary ball mill in an air from 30 to 720 minutes. It was shown that the mechanochemical formation of BiFeO3 (BFO phase was initiated after 60 min and its amount increased gradually with increasing milling time. A detailed XRPD structural analysis is realized by Rietveld’s structure refinement method. The resulting lattice parameters, relative phase abundances, crystallite sizes and crystal lattice microstrains were determined as a function of milling time. Microstructural analysis showed a little difference in morphology of obtained powders. The primary particles, irregular in shape and smaller than 400 nm are observed clearly, although they have assembled together to form agglomerates with varying size and morphology. Dense BFO ceramics were prepared by conventional solid-state reaction at the temperature of 810ºC for 1h followed immediately by quenching process. [Projekat Ministarstva nauke Republike Srbije, br. III45007: Zero- to Three-Dimensional Nanostructures for Application in Electronics and Renewable Energy Sources: Synthesis, Characterization and Processing

  16. Asymmetric catalysis in organic synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Reilly, S.D.; Click, D.R.; Grumbine, S.K.; Scott, B.L.; Watkins, J.G.

    1998-11-01

    This is the final report of a three-year, Laboratory Directed Research and Development (LDRD) project at the Los Alamos National Laboratory (LANL). The goal of the project was to prepare new catalyst systems, which would perform chemical reactions in an enantioselective manner so as to produce only one of the possible optical isomers of the product molecule. The authors have investigated the use of lanthanide metals bearing both diolate and Schiff-base ligands as catalysts for the enantioselective reduction of prochiral ketones to secondary alcohols. The ligands were prepared from cheap, readily available starting materials, and their synthesis was performed in a ''modular'' manner such that tailoring of specific groups within the ligand could be carried out without repeating the entire synthetic procedure. In addition, they have developed a new ligand system for Group IV and lanthanide-based olefin polymerization catalysts. The ligand system is easily prepared from readily available starting materials and offers the opportunity to rapidly prepare a wide range of closely related ligands that differ only in their substitution patterns at an aromatic ring. When attached to a metal center, the ligand system has the potential to carry out polymerization reactions in a stereocontrolled manner.

  17. De novo Synthesis of Monosaccharides

    Science.gov (United States)

    Vogel, Pierre; Robina, Inmaculada

    Recent approaches to asymmetric total synthesis of monosaccharides and derivatives are reviewed. They imply biochemical methods or chemical methods, or combinations of both. Aldoses, alditols, deoxysugars, aminodeoxymonosaccharides, and their analogues are considered, including aza- and thiosugars (with nitrogen and sulfur in the pyranose or furanose ring). Most common monosaccharides have three to six carbon-chains, but examples of long-chain and branched-chain carbohydrates will also be described. Organization of the review is based on the synthetic methodology rather than on the types of targeted sugar, starting with aldolase-catalyzed aldol reactions of achiral precursors, and the now popular amino-acid-catalyzed aldol and Mannich reactions. Chain elongations of small aldose derivatives with one, two, three, or four carbons remain very useful approaches as they allow one to reach a large structural and stereochemical diversity. Other methods apply Diels-Alder or hetero-Diels-Alder additions. Enantiomerically pure monosaccharides have been derived from achiral alkene, diene, and triene derivatives. Almost any targeted natural or non-natural sugar and derivative can be obtained in a few synthetic steps from inexpensive starting materials.

  18. Stereodivergent synthesis with a programmable molecular machine

    Science.gov (United States)

    Kassem, Salma; Lee, Alan T. L.; Leigh, David A.; Marcos, Vanesa; Palmer, Leoni I.; Pisano, Simone

    2017-09-01

    It has been convincingly argued that molecular machines that manipulate individual atoms, or highly reactive clusters of atoms, with Ångström precision are unlikely to be realized. However, biological molecular machines routinely position rather less reactive substrates in order to direct chemical reaction sequences, from sequence-specific synthesis by the ribosome to polyketide synthases, where tethered molecules are passed from active site to active site in multi-enzyme complexes. Artificial molecular machines have been developed for tasks that include sequence-specific oligomer synthesis and the switching of product chirality, a photo-responsive host molecule has been described that is able to mechanically twist a bound molecular guest, and molecular fragments have been selectively transported in either direction between sites on a molecular platform through a ratchet mechanism. Here we detail an artificial molecular machine that moves a substrate between different activating sites to achieve different product outcomes from chemical synthesis. This molecular robot can be programmed to stereoselectively produce, in a sequential one-pot operation, an excess of any one of four possible diastereoisomers from the addition of a thiol and an alkene to an α,β-unsaturated aldehyde in a tandem reaction process. The stereodivergent synthesis includes diastereoisomers that cannot be selectively synthesized through conventional iminium-enamine organocatalysis. We anticipate that future generations of programmable molecular machines may have significant roles in chemical synthesis and molecular manufacturing.

  19. Synthesis of Siloxanes Directly from Amorphous Silica

    International Nuclear Information System (INIS)

    Myint Sandar Win

    2011-12-01

    A direct synthesis of oligomeric-siloxanes from amorphous silica has been achieved. The compound prepared was caedonal-siloxane. Cardonal is a mono hydroxyphenolic compound with a bulky group in the meta position. It was derived as a by-product from the renewable resources cashew nut shell liquid (CNSL). In the synthesis, one pot synthesis was carried out by using ethylene glycol (EG) as solvent. In the reaction ethylene glycol served as a primary precursor chelating ligand in the synthesised product. The one pot synthesis was enhanced by the strong base, triethylenetetramine (TETA) which served as the promoter catalyst. In the synthesis, optimal conditions were established on the basic of the yield percent of organo-siloxane compounds with respect to the variation of the weight fraction of TETA and to the variation of reaction time. Experimental runs were carried out at (ca 210 2c) which was nearly above the boiling point of the solvent. The substituted organo-silicon compounds obtained were characterized by FT- ir, Thermal analysis, XRD and SEM.

  20. Microwave mediated synthesis of semiconductor quantum dots

    Energy Technology Data Exchange (ETDEWEB)

    Afrasiabi, Roodabeh; Sugunan, Abhilash; Shahid, Robina; Toprak, Muhammet S.; Muhammed, Mamoun [Division of Functional Materials, Royal Institute of Technology (KTH), Stockholm (Sweden)

    2012-07-15

    Colloidal quantum dots (QD) have tuneable optoelectronic properties and can be easily handled by simple solution processing techniques, making them very attractive for a wide range of applications. Over the past decade synthesis of morphology controlled high quality (crystalline, monodisperse) colloidal QDs by thermal decomposition of organometallic precursors has matured and is well studied. Recently, synthesis of colloidal QDs by microwave irradiation as heating source is being studied due to the inherently different mechanisms of heat transfer, when compared to solvent convection based heating. Under microwave irradiation, polar precursor molecules directly absorb the microwave energy and heat up more efficiently. Here we report synthesis of colloidal II-VI semiconductor QDs (CdS, CdSe, CdTe) by microwave irradiation and compare it with conventional synthesis based on convection heating. Our findings show that QD synthesis by microwave heating is more efficient and the chalcogenide precursor strongly absorbs the microwave radiation shortening the reaction time and giving a high reaction yield (copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  1. Modelling of the enzymatic kinetically controlled synthesis of cephalexin

    NARCIS (Netherlands)

    Schroën, C.G.P.H.; Fretz, C.B.; Bruin, de V.H.; Berendsen, W.; Moody, H.M.; Roos, E.C.; Roon, van J.L.; Kroon, P.J.; Strubel, M.; Janssen, A.E.M.; Tramper, J.

    2002-01-01

    In this study the influence of diffusion limitation on enzymatic kinetically controlled cephalexin synthesis from phenylglycine amide and 7-aminodeacetoxycephalosporinic acid (7-ADCA) was investigated systematically. It was found that if diffusion limitation occurred, both the synthesis/hydrolysis

  2. Sustainable Alternatives for the Synthesis of Organics and Nanomaterials

    Science.gov (United States)

    The presentation summarizes recent activity in eco-friendly chemical synthesis, which involves benign alternatives, such as the use of supported reagents, and greener reaction medium in aqueous or solvent-free conditions. The synthesis of heterocyclic compounds, coupling reaction...

  3. RNA synthesis during cleavage of the Lymnaea egg

    NARCIS (Netherlands)

    Biggelaar, J.A.M. van den

    In eggs of Lymnaea RNA synthesis can be detected autoradiographically from the 8- to the 16-cell stage. From the 16- to the 24-cell stage distinct nucleoli reappear which are immediately engaged in RNA synthesis.

  4. Versatile three-component procedure for combinatorial synthesis of ...

    Indian Academy of Sciences (India)

    10. In recent years, several methods for the synthesis of spiro-oxindoles with fused 4H-chromenes via multi- component condensation reactions have been reported. The conventional synthesis involves a three-component condensation of ...

  5. PROTEIN SYNTHESIS INHIBITION AND MEMORY: FORMATION VS AMNESIA1

    OpenAIRE

    Gold, Paul E.

    2007-01-01

    Studies using protein synthesis inhibitors have provided key support for the prevalent view that memory formation requires the initiation of protein synthesis as a primary element of the molecular biology of memory. However, many other interpretations of the amnesia data have received far less attention. These include: a) Protein synthesis may play a constitutive role in memory formation, providing proteins prior to an experience that can be activated by training; b) Protein synthesis may be ...

  6. Synthesis of radio-metallofullerenols

    International Nuclear Information System (INIS)

    Keisuke Sueki; Yu Iwai

    2005-01-01

    Water-soluble fullerene derivatives have been investigated to date mostly within the framework of biological and medical applications. For example, C 60 derivatives have been applied as HIV inhibitors, radical scavenging capabilities and anti-cancer. The C 60 fullerenols, C 60 (OH) n , have been synthesized and have shown excellent water solubility. Kitazawa and co-workers also reported a more efficient reaction to obtain C 60 (OH) n , using NaOH aq and tetrabutylammonium hydroxide as a phase transfer catalyst. Water-soluble endohedral metallofullerene derivatives are particularly interesting because of their possible applications to radiotracers and magnetic resonance imaging (MRI) contrast agents. We investigate to trace the synthesis process of metallofullalnols using radioactivity, and obtain the effective process of radio-metallofullerenols. Carbon soot containing Sm endohedoral metallofullerenes was produced by the dc arc discharge method. The resulting soot was extracted with o-dichlorobenzene by reflux for 5 h. The obtained crude was irradiated for 30 min in the JRR4, After irradiation, crude was dissolved by toluene and filtrated by 0.2 μm pore size filter. The separation of the Sm doped C 82 including 153 Sm tracer from the crude was achieved by HPLC method which is a HPLC process on the Buckyprep column. We obtained fraction containing of three kinds of Sm doped C 82 . Details of the syntheses of endohedral metallofullerenols have been reported elsewhere. Briefly, toluene solutions of isolated Sm doped C 82 including 153 Sm with C 60 were vigorously vibrated with saturation KOH aq containing few drops of TBAH (10 % in water) as catalyst at room temperature. The reaction times were changed from l minute to 8 hours. The reaction mixture was filtrated by 0.2 μm filter. The residue was rinsed with methanol to ensure the removal of the catalyst and KOH. The rinsed residue was dissolved in water for 7 hours. The resultant brown- solution was the passed down

  7. Synthesis of Zirconium Lower Chlorides

    International Nuclear Information System (INIS)

    Gaviria, Juan P.

    2002-01-01

    This research is accurately related to the Halox concept of research reactor spent fuel element treatment.The aim of this project is to work the conditioning through selected chlorination of the element that make the spent fuel element. This research studied the physical chemistry conditions which produce formation of the lower zirconium chlorides through the reaction between metallic Zr and gaseous ZrCl 4 in a silica reactor.This work focused special attention in the analysis and confrontation of the published results among the different authors in order to reveal coincidences and contradictions.Experimental section consisted in a set of synthesis with different reaction conditions and reactor design. After reaction were analyzed the products on Zr shavings and the deposit growth on wall reactor.The products were strongly dependent of reactor design. It was observed that as the distance between Zr and wall reactor increased greater was tendency to lower chlorides formation.In reactors with small distance the reaction follows other way without formation of lower chlorides.Analysis on deposit growth on reactor showed that may be formed to a mixture of Si x Zr y intermetallics and zirconium oxides.Presence of oxygen in Zr and Zr-Si compounds on wall reactor reveals that there is an interaction between quartz and reactants.This interaction is in gaseous phase because contamination is observed in experiences where Zr was not in contact with reactor.Finally, it was made a global analysis of all experiences and a possible mechanism that interprets reaction ways is proposed

  8. Quantum chemistry-assisted synthesis route development

    International Nuclear Information System (INIS)

    Hori, Kenji; Sumimoto, Michinori; Murafuji, Toshihiro

    2015-01-01

    We have been investigating “quantum chemistry-assisted synthesis route development” using in silico screenings and applied the method to several targets. Another example was conducted to develop synthesis routes for a urea derivative, namely 1-(4-(trifluoromethyl)-2-oxo-2H-chromen-7-yl)urea. While five synthesis routes were examined, only three routes passed the second in silico screening. Among them, the reaction of 7-amino-4-(trifluoromethyl)-2H-chromen-2-one and O-methyl carbamate with BF 3 as an additive was ranked as the first choice for synthetic work. We were able to experimentally obtain the target compound even though its yield was as low as 21 %. The theoretical result was thus consistent with that observed. The summary of transition state data base (TSDB) is also provided. TSDB is the key to reducing time of in silico screenings

  9. Quantum chemistry-assisted synthesis route development

    Energy Technology Data Exchange (ETDEWEB)

    Hori, Kenji; Sumimoto, Michinori [Graduate School of Science and Engineering, Yamaguchi University, Tokiwadai, Ube, Yamaguchi 755-8611 (Japan); Murafuji, Toshihiro [Graduate School of Medicine, Yamaguchi University, Yamaguchi, Yamaguchi 753-8512 (Japan)

    2015-12-31

    We have been investigating “quantum chemistry-assisted synthesis route development” using in silico screenings and applied the method to several targets. Another example was conducted to develop synthesis routes for a urea derivative, namely 1-(4-(trifluoromethyl)-2-oxo-2H-chromen-7-yl)urea. While five synthesis routes were examined, only three routes passed the second in silico screening. Among them, the reaction of 7-amino-4-(trifluoromethyl)-2H-chromen-2-one and O-methyl carbamate with BF{sub 3} as an additive was ranked as the first choice for synthetic work. We were able to experimentally obtain the target compound even though its yield was as low as 21 %. The theoretical result was thus consistent with that observed. The summary of transition state data base (TSDB) is also provided. TSDB is the key to reducing time of in silico screenings.

  10. Green Chemistry Techniques for Gold Nanoparticles Synthesis

    Science.gov (United States)

    Cannavino, Sarah A.; King, Christy A.; Ferrara, Davon W.

    Gold nanoparticles (AuNPs) are often utilized in many technological and research applications ranging from the detection of tumors, molecular and biological sensors, and as nanoantennas to probe physical processes. As these applications move from the research laboratory to industrial settings, there is a need to develop efficient and sustainable synthesis techniques. Recent research has shown that several food products and beverages containing polyphenols, a common antioxidant, can be used as reducing agents in the synthesis of AuNPs in solution. In this study, we explore a variety of products to determine which allow for the most reproducible solution of nanoparticles based on the size and shapes of particles present. We analyzed the AuNPs solutions using extinction spectroscopy and atomic force microscopy. We also develop a laboratory activity to introduce introductory chemistry and physics students to AuNP synthesis techniques and analysis.

  11. Inorganic materials synthesis in ionic liquids

    Directory of Open Access Journals (Sweden)

    Christoph Janiak

    2014-01-01

    Full Text Available The field of "inorganic materials from ionic liquids" (ILs is a young and dynamically growing research area for less than 10 years. The ionothermal synthesis in ILs is often connected with the preparation of nanomaterials, the use of microwave heating and in part also ultrasound. Inorganic material synthesis in ILs allows obtaining phases which are not accessible in conventional organic or aqueous solvents or with standard methods of solid-state chemistry or under such mild conditions. Cases at hand include "ligand-free" metal nanoparticles without added stabilizing capping ligands, inorganic or inorganic-organic hybrid solid-state compounds, large polyhedral clusters and exfoliated graphene from low-temperature synthesis. There are great expectations that ILs open routes towards new, possibly unknown, inorganic materials with advantageous properties that cannot (or only with great difficulty be made via conventional processes.

  12. An efficient synthesis of loline alkaloids

    Science.gov (United States)

    Cakmak, Mesut; Mayer, Peter; Trauner, Dirk

    2011-07-01

    Loline (1) is a small alkaloid that, in spite of its simple-looking structure, has posed surprising challenges to synthetic chemists. It has been known for more than a century and has been the subject of extensive biological investigations, but only two total syntheses have been achieved to date. Here, we report an asymmetric total synthesis of loline that, with less then ten steps, is remarkably short. Our synthesis incorporates a Sharpless epoxidation, a Grubbs olefin metathesis and an unprecedented transannular aminobromination, which converts an eight-membered cyclic carbamate into a bromopyrrolizidine. The synthesis is marked by a high degree of chemo- and stereoselectivity and gives access to several members of the loline alkaloid family. It delivers sufficient material to support a programme aimed at studying the complex interactions between plants, fungi, insects and bacteria brokered by loline alkaloids.

  13. A review: radiolabeled synthesis of pesticides

    International Nuclear Information System (INIS)

    Li Juying; Han Ailiang; Wang Haiyan; Wang Wei; Ye Qingfu

    2010-01-01

    Isotope tracer technique has been widely applied in studies of metabolism, mode action, fate and environmental behavior of pesticides. In such studies, the key point is to obtain suitable radiolabelled compounds. However, the radiotracers, especially the labelled pesticides which are novel compounds with complex structures and longer synthesis routes, are usually unavailable from domestic and /or foreign markets. Therefore, it is essential to explore the synthesis methods of radiolabelled pesticides, which are quite different from the conventional nonradiosynthesis, and are requested to obtain higher yield. This article is a review on current status of choosing the available radionuclide and labelled position, the main synthesis methods and problems in the process of preparing radiolabelled pesticides. (authors)

  14. Computer-assisted spectral design and synthesis

    Science.gov (United States)

    Vadakkumpadan, Fijoy; Wang, Qiqi; Sun, Yinlong

    2005-01-01

    In this paper, we propose a computer-assisted approach for spectral design and synthesis. This approach starts with some initial spectrum, modifies it interactively, evaluates the change, and decides the optimal spectrum. Given a requested change as function of wavelength, we model the change function using a Gaussian function. When there is the metameric constraint, from the Gaussian function of request change, we propose a method to generate the change function such that the result spectrum has the same color as the initial spectrum. We have tested the proposed method with different initial spectra and change functions, and implemented an interactive graphics environment for spectral design and synthesis. The proposed approach and graphics implementation for spectral design and synthesis can be helpful for a number of applications such as lighting of building interiors, textile coloration, and pigment development of automobile paints, and spectral computer graphics.

  15. Mapping Out Biogenetic Hypotheses by Chemical Synthesis.

    Science.gov (United States)

    Liffert, Raphael; Gademann, Karl

    2017-12-01

    Synthesis of natural products via their postulated or established biosynthetic intermediates ('biomimetic synthesis' or 'bio-inspired synthesis') has the power to identify both yet undiscovered intermediates and undiscovered mechanistic pathways for their formation. In this account, we report on our recent studies on unusual hypotheses for biosynthetic transformations, such as a late-stage aldol reaction (periconianone A), benzilic acid rearrangement (taiwaniaquinone H), a redox-neutral light-driven C-H activation (taiwaniaquinol A and cyclocoulterone), a hetero Diels-Alder reaction (obtusinones), aziridinium chemistry (Securinega alkaloids), and a [3+2] nitrone olefin cycloaddition (virosaine A). All these studies provided evidence on the molecular level for the feasibility of these transformations, and suggest that further studies investigating the relevance of these hypotheses in biological systems are warranted.

  16. Processing of hydroxyapatite obtained by combustion synthesis

    International Nuclear Information System (INIS)

    Canillas, M.; Rivero, R.; García-Carrodeguas, R.; Barba, F.; Rodríguez, M.A.

    2017-01-01

    One of the reasons of implants failure are the stress forces appearing in the material–tissue interface due to the differences between their mechanical properties. For this reason, similar mechanical properties to the surrounding tissue are desirable. The synthesis of hydroxyapatite by solution combustion method and its processing have been studied in order to obtain fully dense ceramic bodies with improved mechanical strength. Combustion synthesis provides nanostructured powders characterized by a high surface area to facilitate the following sintering. Moreover, synthesis was conducted in aqueous and oxidizing media. Oxidizing media improve homogenization and increase the energy released during combustion. It gives rise to particles whose morphology and size suggest lower surface energies compared with aqueous media. The obtained powders were sintered by using a controlled sintering rate schedule. Lower surfaces energies minimize the shrinkage during sintering and relative densities measurements and diametral compression test confirm improved densification and consequently mechanical properties. [es

  17. Processing of hydroxyapatite obtained by combustion synthesis

    Directory of Open Access Journals (Sweden)

    M. Canillas

    2017-09-01

    Full Text Available One of the reasons of implants failure are the stress forces appearing in the material–tissue interface due to the differences between their mechanical properties. For this reason, similar mechanical properties to the surrounding tissue are desirable. The synthesis of hydroxyapatite by solution combustion method and its processing have been studied in order to obtain fully dense ceramic bodies with improved mechanical strength. Combustion synthesis provides nanostructured powders characterized by a high surface area to facilitate the following sintering. Moreover, synthesis was conducted in aqueous and oxidizing media. Oxidizing media improve homogenization and increase the energy released during combustion. It gives rise to particles whose morphology and size suggest lower surface energies compared with aqueous media. The obtained powders were sintered by using a controlled sintering rate schedule. Lower surfaces energies minimize the shrinkage during sintering and relative densities measurements and diametral compression test confirm improved densification and consequently mechanical properties.

  18. Asymmetric synthesis II more methods and applications

    CERN Document Server

    Christmann, Mathias

    2012-01-01

    After the overwhelming success of 'Asymmetric Synthesis - The Essentials', narrating the colorful history of asymmetric synthesis, this is the second edition with latest subjects and authors. While the aim of the first edition was mainly to honor the achievements of the pioneers in asymmetric syntheses, the aim of this new edition was bringing the current developments, especially from younger colleagues, to the attention of students. The format of the book remained unchanged, i.e. short conceptual overviews by young leaders in their field including a short biography of the authors. The growing multidisciplinary research within chemistry is reflected in the selection of topics including metal catalysis, organocatalysis, physical organic chemistry, analytical chemistry, and its applications in total synthesis. The prospective reader of this book is a graduate or undergraduate student of advanced organic chemistry as well as the industrial chemist who wants to get a brief update on the current developments in th...

  19. Synthesis and processing of nanostructured materials

    International Nuclear Information System (INIS)

    Siegel, R.W.

    1992-12-01

    Significant and growing interest is being exhibited in the novel and enhanced properties of nanostructured materials. These materials, with their constituent phase or grain structures modulated on a length scale less than 100 nm, are artificially synthesized by a wide variety of physical, chemical, and mechanical methods. In this NATO Advanced Study Institute, where mechanical behavior is emphasized, nanostructured materials with modulation dimensionalities from one (multilayers) to three (nanophase materials) are mainly considered. No attempt is made in this review to cover in detail all of the diverse methods available for the synthesis of nanostructured materials. Rather, the basic principles involved in their synthesis are discussed in terms of the special properties sought using examples of particular synthesis and processing methodologies. Some examples of the property changes that can result from one of these methods, cluster assembly of nanophase materials, are presented

  20. Synthesis, Transfer, and Characterization of Nanoscale 2-Dimensional Materials

    Science.gov (United States)

    2015-09-01

    stack is floating on top of the DDI water surface. Instead of removing the stack with the target substrate, a graphene/copper foil substrate (graphene...demonstrated the synthesis of graphene, hexagonal boron nitride, and bismuth telluride using chemical and physical vapor deposition techniques. Making...for material synthesis, transfer, and characterization. 15. SUBJECT TERMS graphene, hexagonal boron nitride, bismuth telluride, synthesis, transfer