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Sample records for acrylonitrile

  1. Toxicologic profile of acrylonitrile.

    Science.gov (United States)

    Woutersen, R A

    1998-01-01

    Acrylonitrile is a monomer used extensively as a raw material in the manufacturing of acrylic fibers, plastics, synthetic rubbers, and acrylamide. It has been classified as a probable human carcinogen according to the results of numerous chronic rat bioassays. The present report summarizes the toxicity data on acrylonitrile and reviews available data concerning the mechanism (genetic versus epigenetic) by which acrylonitrile is carcinogenic in rats. From the evaluation of the relevant toxicity data, it can be concluded that acrylonitrile is indeed carcinogenic to rats after either oral or inhalational exposure. However, information on other mammalian species is lacking, and, moreover, the exact mechanism of the carcinogenic process is unclear. Therefore, it is recommended to conduct an additional long-term inhalation carcinogenicity study with acrylonitrile in mice, as well as studies into the mechanism by which acrylonitrile induces (brain) tumors in rats (genetic versus epigenetic).

  2. Acrylonitrile: a suspected human carcinogen.

    Science.gov (United States)

    Koerselman, W; van der Graaf, M

    1984-01-01

    The literature on carcinogenicity of acrylonitrile (an important intermediate in the chemical industry) is reviewed. The three main conclusions are: (1) Acrylonitrile has genotoxic effects in various tests in microorganisms and in mammal cells. (2) Chronic exposure to acrylonitrile causes tumours in rats. (3) Results of epidemiological studies indicate that acrylonitrile may be a human carcinogen. From this it is clear that acrylonitrile is very probably carcinogenic to humans. Therefore the authors plead for a reduction of acrylonitrile standards to the lowest practicable limit.

  3. Toxicologic profile of acrylonitrile

    NARCIS (Netherlands)

    Woutersen, R.A.

    1998-01-01

    Acrylonitrile is a monomer used extensively as a raw material in the manufacturing of acrylic fibers, plastics, synthetic rubbers, and acrylamide. It has been classified as a probable human carcinogen according to the results of numerous chronic rat bioassays. The present report summarizes the toxic

  4. The acrylonitrile dimer ion

    Science.gov (United States)

    Ervasti, Henri K.; Jobst, Karl J.; Burgers, Peter C.; Ruttink, Paul J. Ae; Terlouw, Johan K.

    2007-04-01

    Large energy barriers prohibit the rearrangement of solitary acrylonitrile ions, CH2CHCN+, into their more stable hydrogen-shift isomers CH2CCNH+ or CHCH-CNH+. This prompted us to examine if these isomerizations occur by self-catalysis in acrylonitrile dimer ions. Such ions, generated by chemical ionization experiments of acrylonitrile with an excess of carbon dioxide, undergo five dissociations in the [mu]s time frame, as witnessed by peaks at m/z 53, 54, 79, 80 and 105 in their metastable ion mass spectrum. Collision experiments on these product ions, deuterium labeling, and a detailed computational analysis using the CBS-QB3 model chemistry lead to the following conclusions: (i) the m/z 54 ions are ions CH2CHCNH+ generated by self-protonation in ion-dipole stabilized hydrogen-bridged dimer ions [CH2CHCN...H-C(CN)CH2]+ and [CH2CHCN...H-C(H)C(H)CN]+; the proton shifts in these ions are associated with a small reverse barrier; (ii) dissociation of the H-bridged ions into CH2CCNH+ or CHCH-CNH+ by self-catalysis is energetically feasible but kinetically improbable: experiment shows that the m/z 53 ions are CH2CHCN+ ions, generated by back dissociation; (iii) the peaks at m/z 79, 80 and 105 correspond with the losses of HCN, C2H2 and H, respectively. The calculations indicate that these ions are generated from dimer ions that have adopted the (much more stable) covalently bound "head-to-tail" structure [CH2CHCN-C(H2)C(H)CN]+; experiments indicate that the m/z 79 (C5H5N) and m/z 105 (C6H6N2) ions have linear structures but the m/z 80 (C4H4N2) ions consist of ionized pyrimidine in admixture with its stable pyrimidine-2-ylidene isomer. Acrylonitrile is a confirmed species in interstellar space and our study provides experimental and computational evidence that its dimer radical cation yields the ionized prebiotic pyrimidine molecule.

  5. Biobased synthesis of acrylonitrile from glutamic acid

    NARCIS (Netherlands)

    Notre, le J.E.L.; Scott, E.L.; Franssen, M.C.R.; Sanders, J.P.M.

    2011-01-01

    Glutamic acid was transformed into acrylonitrile in a two step procedure involving an oxidative decarboxylation in water to 3-cyanopropanoic acid followed by a decarbonylation-elimination reaction using a palladium catalyst

  6. Acrylonitrile-induced oxidative DNA damage in rat astrocytes.

    Science.gov (United States)

    Pu, Xinzhu; Kamendulis, Lisa M; Klaunig, James E

    2006-10-01

    Chronic administration of acrylonitrile results in a dose-related increase in astrocytomas in rat brain, but the mechanism of acrylonitrile carcinogenicity is not fully understood. The potential of acrylonitrile or its metabolites to induce direct DNA damage as a mechanism for acrylonitrile carcinogenicity has been questioned, and recent studies indicate that the mechanism involves the induction of oxidative stress in rat brain. The present study examined the ability of acrylonitrile to induce DNA damage in the DI TNC1 rat astrocyte cell line using the alkaline Comet assay. Oxidized DNA damage also was evaluated using formamidopyrimidine DNA glycosylase treatment in the modified Comet assay. No increase in direct DNA damage was seen in astrocytes exposed to sublethal concentrations of acrylonitrile (0-1.0 mM) for 24 hr. However, acrylonitrile treatment resulted in a concentration-related increase in oxidative DNA damage after 24 hr. Antioxidant supplementation in the culture media (alpha-tocopherol, (-)-epigallocathechin-3 gallate, or trolox) reduced acrylonitrile-induced oxidative DNA damage. Depletion of glutathione using 0.1 mM DL-buthionine-[S,R]-sulfoximine increased acrylonitrile-induced oxidative DNA damage (22-46%), while cotreatment of acrylonitrile with 2.5 mM L-2-oxothiazolidine-4-carboxylic acid, a precursor for glutathione biosynthesis, significantly reduced acrylonitrile-induced oxidative DNA damage (7-47%). Cotreatment of acrylonitrile with 0.5 mM 1-aminobenzotriazole, a suicidal inhibitor of cytochrome P450, prevented the oxidative DNA damage produced by acrylonitrile. Cyanide (0.1-0.5 mM) increased oxidative DNA damage (44-160%) in astrocytes. These studies demonstrate that while acrylonitrile does not directly damage astrocyte DNA, it does increase oxidative DNA damage. The oxidative DNA damage following acrylonitrile exposure appears to arise mainly through the P450 metabolic pathway; moreover, glutathione depletion may contribute to the

  7. Biological monitoring of acrylonitrile exposure

    Energy Technology Data Exchange (ETDEWEB)

    Houthuijs, D.; Remijn, B.; Willems, H.; Boleij, J.; Biersteker, K.

    1982-01-01

    A study was made of the excretion pattern of acrylonitrile (AN) in urine of 15 AN-exposed workers. During a 7-day working period with the following 2 days off, the workers delivered all their urines separately. Exposure data, collected by personal monitoring, showed a mean 8-hour TWA value of 0.13 ppm. The excretion of AN in urine (AN(U) ) showed a typical pattern; concentrations peaked at the end or shortly after the end of the workday and decreased rapidly until the beginning of the next workday. A control group of 41 nonexposed workers of the same company showed a significant increase of AN(U) with increasing number of cigarettes smoked. The AN(U) concentrations of the exposed workers however were, despite the low exposure, much higher than those of the controls, both during the workdays and during the days off. Biological monitoring of AN-exposed workers by assessing AN(U) therefore seems a very sensitive exposure evaluation method, especially because it accounts for inhalation as well as skin penetration as routes for entering the body.

  8. 21 CFR 181.32 - Acrylonitrile copolymers and resins.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Acrylonitrile copolymers and resins. 181.32 Section... Ingredients § 181.32 Acrylonitrile copolymers and resins. (a) Acrylonitrile copolymers and resins listed in... of the vinyl chloride resin) resin—for use only in contact with oleomargarine. (iv)...

  9. Starch Modification by Graft Copolymerization of Acrylonitrile

    Institute of Scientific and Technical Information of China (English)

    刘瑞贤; 李莉; 茹宗玲; 张黎明; 高建平; 田汝川

    2003-01-01

    The graft copolymerization of acrylonitrile (AN) onto starch under the initiation of potassium permanganate was investigated. The effect of various reaction conditions on the graft copolymerization was studied. The relationships between the grafting rate and the initiator concentration of potassium permanganate, monomer acrylonitrile and backbone starch, as well as reaction temperature were established. The oxidation reaction of starch with manganic ions and valence changes of manganic ions during the graft copolymerization were discussed. The results show that manganic ion Mn7+ underwent a series of valence changes during the graft copolymerization: Mn(Ⅶ) → Mn(Ⅳ) → Mn(Ⅲ) → Mn(Ⅱ). The grafting rate of the graft copolymerization of acrylonitrile onto starch is also given.

  10. Cancer occurrence among workers exposed to acrylonitrile.

    Science.gov (United States)

    Rothman, K J

    1994-10-01

    A MEDLINE search identified 12 published epidemiologic studies that have reported incidence or mortality experience among workers exposed to acrylonitrile. Many of the studies contain scanty descriptions of subject ascertainment, and most do not have good information on exposure assessment. Many also may have suffered from incomplete follow-up, as evinced by an overall deficit in the number of deaths observed, compared with the number expected from general population mortality rates. Such problems are not unique to studies on acrylonitrile, and to some extent they reflect the difficulties of conducting retrospective cohort studies. Despite these drawbacks, a simplified meta-analysis of the mortality experience reported for these cohorts revealed little evidence for carcinogenicity. Approximately the same number of cancer deaths was observed as was expected according to general population mortality rates (standardized mortality ratio 1.03, 90% confidence interval 0.92-1.15). The combined information from these studies is insufficient to support confidence about a lack of carcinogenicity at all sites. Nevertheless, despite the flaws in some of the individual studies, the summarized findings offer reassurance that workers exposed to acrylonitrile face no striking increases in mortality for all cancers or for respiratory cancer.

  11. 21 CFR 177.1480 - Nitrile rubber modified acrylonitrile-methyl acrylate copolymers.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Nitrile rubber modified acrylonitrile-methyl... Nitrile rubber modified acrylonitrile-methyl acrylate copolymers. Nitrile rubber modified acrylonitrile... rubber modified acrylonitrile-methyl acrylate copolymers consist of basic copolymers produced by...

  12. Information draft on the development of air standards for acrylonitrile

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1999-01-01

    Acrylonitrile is a colourless liquid with a faintly sweet and pungent odour. It is widely used as a chemical intermediate in a variety of industrial and commercial products such as acrylic and modacrylic fibres, plastics, styrene-acrylonitrile, nitrile rubber resins, and acrylamide. Although not currently produced in Canada, acrylonitrile is used in the manufacture of industrial and commercial products. Acrylonitrile levels around end-use plants have been found to be significantly higher than at producing facilities. Almost all releases of acrylonitrile are to the atmosphere and one facility is responsible for all releases in Ontario. Human exposure is through air, water and food. Acrylonitrile is absorbed by inhalation, through the mouth and to some extent through the skin. Exposure at concentrations of 7 to 45 microgram/cubic meter for 20 to 45 minutes leads to irritation of the mucous membranes, nausea, headaches, and irritability. Low-grade anaemia, leukocytosis, kidney irritation and mild jaundice have also been observed. Children are more sensitive than adults. Acrylonitrile is classified as probable human carcinogen by the US Environmental Protection Agency. The current ambient air quality criterion (AAQC) in Ontario is 100 microgram/cubic metre and the half-hour interim point of impingement (POI) standard is 300 microgram/cubic meter. Review of world-wide literature showed the existence of standards in several American states. Cancer unit risks estimates have been made by the US Environmental Protection Agency as well as by the World Health Organization. 63 refs., 1 tab., appendix.

  13. Effect of acrylonitrile on the electrode processes ivolving copper cations

    Directory of Open Access Journals (Sweden)

    Viktor F. Vargalyuk

    2016-03-01

    Full Text Available Based on the results of cyclic voltammetry and study of deposits morphology, it has been shown that acrylonitrile does not have significant effect on the mechanism of Cu2+ + 2ē → Cu0 reaction. This distinguishes acrylonitrile from the unsaturated polyfunctional organic substances (acrylic acid, acrylamide which forms stable complexes with Cu2+ ions. Acrylonitrile just inhibits cathodic process by adsorbing on the surface of electrode thus blocking its active sites. But the presence of acrylonitrile significantly changes the mechanism of the anodic process. It has been found that acrylonitrile interacts with surface copper atoms thus forming thermodynamically stable [Cu π-AN]0 π‑complexes. Ionization potential of these π‑complexes is more negative if compare to copper atoms. As the result acceleration of anodic process takes place in the low polarization area. However, since the chemisorption is a slow process the presence of acrylonitrile mainly affects dissolution of the first surface layers of copper atoms. Further ionization of copper atoms runs out directly and requires higher polarization.

  14. Mutagenicity, carcinogenicity, and teratogenicity of acrylonitrile.

    Science.gov (United States)

    Léonard, A; Gerber, G B; Stecca, C; Rueff, J; Borba, H; Farmer, P B; Sram, R J; Czeizel, A E; Kalina, I

    1999-05-01

    Acrylonitrile (AN) is an important intermediary for the synthesis of a variety of organic products, such as artificial fibres, household articles and resins. Although acute effects are the primary concern for an exposure to AN, potential genotoxic, carcinogenic and teratogenic risks of AN have to be taken seriously in view of the large number of workers employed in such industries and the world-wide population using products containing and possibly liberating AN. An understanding of the effect of acrylonitrile must be based on a characterization of its metabolism as well as of the resulting products and their genotoxic properties. Tests for mutagenicity in bacteria have in general been positive, those in plants and on unscheduled DNA synthesis doubtful, and those on chromosome aberrations in vivo negative. Wherever positive results had been obtained, metabolic activation of AN appeared to be a prerequisite. The extent to which such mutagenic effects are significant in man depends, however, also on the conditions of exposure. It appears from the limited data that the ultimate mutagenic factor(s), such as 2-cyanoethylene oxide, may have little opportunity to act under conditions where people are exposed because it is formed only in small amounts and is rapidly degraded. The carcinogenic action of AN has been evaluated by various agencies and ranged from 'reasonably be anticipated to be a human carcinogen' to 'cannot be excluded', the most recent evaluation being 'possibly carcinogenic to humans'. Animal data that confirm the carcinogenic potential of AN have certain limitations with respect to the choice of species, type of tumors and length of follow up. Epidemiological studies which sometimes, but not always, yielded positive results, encounter the usual difficulties of confounding factors in chemical industries. Exposure of workers to AN should continue to be carefully monitored, but AN would not have to be considered a cancer risk to the population provided

  15. Survey of volatile substances in kitchen utensils made from acrylonitrile-butadiene-styrene and acrylonitrile-styrene resin in Japan.

    Science.gov (United States)

    Abe, Yutaka; Yamaguchi, Miku; Mutsuga, Motoh; Kawamura, Yoko; Akiyama, Hiroshi

    2014-05-01

    Residual levels of 14 volatile substances, including 1,3-butadiene, acrylonitrile, benzene, ethylbenzene, and styrene, in 30 kitchen utensils made from acrylonitrile-butadiene-styrene resin (ABS) and acrylonitrile-styrene resin (AS) such as slicers, picks, cups, and lunch boxes in Japan were simultaneously determined using headspace gas chromatography/mass spectroscopy (HS-GC/MS). The maximum residual levels in the ABS and AS samples were found to be 2000 and 2800 μg/g of styrene, respectively. The residual levels of 1,3-butadiene ranged from 0.06 to 1.7 μg/g in ABS, and three of 15 ABS samples exceeded the regulatory limit for this compound as established by the European Union (EU). The residual levels of acrylonitrile ranged from 0.15 to 20 μg/g in ABS and from 19 to 180 μg/g in AS. The levels of this substance in seven ABS and six AS samples exceeded the limit set by the U.S. Food and Drug Administration (FDA). Furthermore, the levels of acrylonitrile in three AS samples exceeded the voluntary standard established by Japanese industries. These results clearly indicate that the residual levels of some volatile compounds are still high in ABS and AS kitchen utensils and further observations are needed.

  16. Commercial Application of the XYA-5 Catalyst in Acrylonitrile Unit

    Institute of Scientific and Technical Information of China (English)

    Li Zhengguang

    2008-01-01

    The XYA-5 catalyst was first applied in commercial scale on an 80-kt/a acrylonitrile unit at the Daqing Refining and Chemical Company.Test results had shown that the once-through yield of acrylonitrile exceeded 80% with the unit consumption of propylene reaching 1032 kg on each ton of acryionitrile.The product quality could be easily put under control and the distribution of reaction products was reasonable with good cleaning performance and stability of the catalyst that was suitable for use on this commercial unit.

  17. Radiation-induced graft copolymerization of binary monomer mixture containing acrylonitrile onto polyethylene films

    Science.gov (United States)

    Choi, Seong-Ho; Nho, Young Chang

    2000-04-01

    Graft copolymerization of acrylonitrile (AN)/acrylic acid (AA), acrylonitrile (AN)/methacrylic acid (MA), and acrylonitrile (AN)/glycidyl methacrylate (GMA) onto pre-irradiated polyethylene (PE) films were studied. The effect of reaction conditions such as solvents, additives, and monomer composition on the grafting yields was investigated. The extent of grafting was found to increase with increasing sulfuric acid concentration when sulfuric acid as an additive was added to the grafting solution. In AN/AA mixture, the proportion of acrylonitrile in the copolymer increased with an increasing AN component in feed monomers. On the other hand, in AN/MA mixture, acrylonitrile component in copolymer was very slight in spite of the increase AN component in feed monomers. In the AN/GMA mixture, the proportion of acrylonitrile in the copolymer increased with increasing acrylonitrile component in AN/GMA feed monomer.

  18. Polyacrylamide polymers derived from acrylonitrile without intermediate isolation

    Energy Technology Data Exchange (ETDEWEB)

    Norton, C.J.; Falk, D.O.

    1977-04-05

    Hydrolyzed and neutralized acrylonitrile is polymerized in solution without isolation to produce a high molecular weight polyacrylamide useful for mobility control in secondary recovery of petroleum. The polyacrylamide optionally may be hydrolyzed, methylolated, and sulfomethylated to further enhance its water-thickening properties. This procedure reduces the cost of making polyacrylamide. (5 claims)

  19. A New Quenching Process and Tower to Improve the Recovery of Acrylonitrile

    Institute of Scientific and Technical Information of China (English)

    甘永胜; 顾军民; 方永成

    2004-01-01

    Quenching process and design of the quenching tower in acrylonitrile production in China were studied in order to decrease the polymerization loss of acrylonitrile in the quenching tower. Based on the research of acrylonitrile polymerization in the quenching tower, a new quenching process was proposed to avoid the disadvantages of the original process. Two kinds of internals were installed to improve the performance of the quenching tower. Through a series of air-flow and real-flow model experiments, the new quenching process and new design were showed to be successful in enhancing the mass and heat transfer in the vapor-liquid system and decreasing the loss of acrylonitrile.Industrial application showed satisfactory results of decrease of the acrylonitrile loss in the quenching tower by about 4.5% and increase of the acrylonitrile recovery of the whole plant by more than 4%.

  20. Thermal Stability of Poly (acrylonitrile-methyl acrylate) Copolymers

    Institute of Scientific and Technical Information of China (English)

    HAN Na; ZHANG Xing-xiang; WANG Xue-chen

    2008-01-01

    Poly (acrylonitrile-methyl acrylate) copolymer was synthesized by water depositing polymerization and has a typical feed ratio of 85/15. And then 1 - 3 wt% lauryl alcohol maleic anhydride (LAM) was adopted as stabilizer to mix with the acrylonitrile based copolymer. The mixtures were characterized by using Fourier Transform Infrared Spectroscopy (FTIR), Nuclear Magnetic Resonance (1H NMR ), Gel Permeation Chromatography ( GPC ), Differential Scanning Calorimetry (DSC), optic microscope and Ubbelohde viscosimetryr etc. The melting point (Tm) and glass transition temperature (Tg) of the 85/15 AN/MA copolymer mixed with LAM all decrease with the increase of stabilizer content. The lowest Tg and Tm were 116.1 ℃ and 209. 1℃ respectively at the heating rate of 100℃/min when the content of LAM is 2 wt%. The 85°/15 AN/MA copolymer mixed with 1 - 3 w t% LAM possess good thermal stability up to 30 min at 220 ℃.

  1. Radiation initiated copolymerization of allyl alcohol with acrylonitrile

    Energy Technology Data Exchange (ETDEWEB)

    Solpan, Dilek; Guven, Olgun [Hacettepe Univ., Ankara (Turkey). Dept. of Chemistry

    1996-07-01

    Copolymerization of allyl alcohol (AA) with acrylonitrile (AN) initiated by {gamma}-rays has been investigated to determine the respective reactivity ratios. Three different experimental techniques, namely Fourier Transform Infrared (FTIR), Ultraviolet (UV/vis) and elemental analysis (EA) have been used for the determination of copolymer compositions. Fineman-Ross (FR), Kelen-Tudos (KT), Non-Linear Least Square (NLLS) Analysis and Q-e methods have been applied to the three sets of experimental data. It has been concluded that data obtained from elemental analysis as applied to the Non-Linear Least Square approach gave the most reliable reactivity ratios as 2.09 and 0.40 for acrylonitrile and allyl alcohol, respectively. (Author).

  2. Radiation initiated copolymerization of allyl alcohol with acrylonitrile

    Science.gov (United States)

    Şolpan, Dilek; Güven, Olgun

    1996-07-01

    Copolymerization of allyl alcohol (AA) with acrylonitrile (AN) initiated by γ-rays has been investigated to determine the respective reactivity ratios. Three different experimental techniques, namely Fourier Transform Infrared (FTIR), Ultraviolet (UV/vis) and elemental analysis (EA) have been used for the determination of copolymer compositions. Fineman-Ross (FR), Kelen-Tüdös (KT), Non-Linear Least Square (NLLS) Analysis and Q-e methods have been applied to the three sets of experimental data. It has been concluded that data obtained from elemental analysis as applied to the Non-Linear Least Square approach gave the most reliable reactivity ratios as 2.09 and 0.40 for acrylonitrile and allyl alcohol, respectively.

  3. Hepatoprotective activity of quercetin against acrylonitrile-induced hepatotoxicity in rats.

    Science.gov (United States)

    Abo-Salem, Osama M; Abd-Ellah, Mohamed F; Ghonaim, Mabrouk M

    2011-01-01

    Acrylonitrile is a potent hepatotoxic, mutagen, and carcinogen. A role for free radical-mediated lipid peroxidation in the toxicity of acrylonitrile has been suggested. The present study was designed to assess the hepatoprotective effect of quercetin against acrylonitrile-induced hepatotoxicity in rats. Liver damage was induced by oral administration of acrylonitrile (50 mg/kg/day/5 weeks). Acrylonitrile produced a significant elevation of malondialdehyde (138.9%) with a marked decrease in reduced glutathione (72.4%), and enzymatic antioxidants; superoxide dismutase (81%), and glutathione peroxidase (53.2%) in the liver. Serum aspartate aminotransferase, alanine aminotransferases, direct bilirubin, and total bilirubin showed a significant increase in acrylonitrile alone treated rats (115.5%, 110.8%, 1006.8%, and 1000.8%, respectively). Pretreatment with quercetin (70 mg/kg/day/6 weeks) and its coadministration with acrylonitrile prevented acrylonitrile-induced alterations in hepatic lipid peroxides and enzymatic antioxidants as well as serum aminotransferases and bilirubin. Histopathological findings supported the biochemical results. We suggest that querectin possess hepatoprotective effect against acrylonitrile-induced hepatotoxicity through its antioxidant activity.

  4. Hydrolyzed Poly(acrylonitrile) Electrospun Ion-Exchange Fibers

    OpenAIRE

    Jassal, Manisha; Bhowmick, Sankha; Sengupta, Sukalyan; Patra, Prabir K.; Walker, Douglas I.

    2014-01-01

    A potential ion-exchange material was developed from poly(acrylonitrile) fibers that were prepared by electrospinning followed by alkaline hydrolysis (to convert the nitrile group to the carboxylate functional group). Characterization studies performed on this material using X-ray photoelectron spectroscopy, scanning electron microscopy, Fourier-Transform infra-red spectroscopy, and ion chromatography confirmed the presence of ion-exchange functional group (carboxylate). Optimum hydrolysis co...

  5. 21 CFR 177.1020 - Acrylonitrile/butadiene/sty-rene co-polymer.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Acrylonitrile/butadiene/sty-rene co-polymer. 177... SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances.../butadiene/sty-rene co-polymer. Acrylonitrile/butadiene/styrene copolymer identified in this section may...

  6. 21 CFR 177.1030 - Acrylonitrile/butadiene/styrene/methyl methacrylate copolymer.

    Science.gov (United States)

    2010-04-01

    ... as determined by a method titled “Analysis of Cycopac Resin for Residual β-(2-Hydroxyethylmercapto... the range of 13.0 to 16.0 percent as determined by Micro-Kjeldahl analysis. (2) Residual acrylonitrile... a gas chromatographic method titled “Determination of Residual Acrylonitrile and Styrene...

  7. Kinetic and equilibrium studies of acrylonitrile binding to cytochrome c peroxidase and oxidation of acrylonitrile by cytochrome c peroxidase compound I

    Energy Technology Data Exchange (ETDEWEB)

    Chinchilla, Diana, E-mail: Diana_Chinchilla@yahoo.com; Kilheeney, Heather, E-mail: raindropszoo@yahoo.com; Vitello, Lidia B., E-mail: lvitello@niu.edu; Erman, James E., E-mail: jerman@niu.edu

    2014-01-03

    Highlights: •Cytochrome c peroxidase (CcP) binds acrylonitrile in a pH-independent fashion. •The spectrum of the CcP/acrylonitrile complex is that of a 6c–ls ferric heme. •The acrylonitrile/CcP complex has a K{sub D} value of 1.1 ± 0.2 M. •CcP compound I oxidizes acrylonitrile with a maximum turnover rate of 0.61 min{sup −1}. -- Abstract: Ferric heme proteins bind weakly basic ligands and the binding affinity is often pH dependent due to protonation of the ligand as well as the protein. In an effort to find a small, neutral ligand without significant acid/base properties to probe ligand binding reactions in ferric heme proteins we were led to consider the organonitriles. Although organonitriles are known to bind to transition metals, we have been unable to find any prior studies of nitrile binding to heme proteins. In this communication we report on the equilibrium and kinetic properties of acrylonitrile binding to cytochrome c peroxidase (CcP) as well as the oxidation of acrylonitrile by CcP compound I. Acrylonitrile binding to CcP is independent of pH between pH 4 and 8. The association and dissociation rate constants are 0.32 ± 0.16 M{sup −1} s{sup −1} and 0.34 ± 0.15 s{sup −1}, respectively, and the independently measured equilibrium dissociation constant for the complex is 1.1 ± 0.2 M. We have demonstrated for the first time that acrylonitrile can bind to a ferric heme protein. The binding mechanism appears to be a simple, one-step association of the ligand with the heme iron. We have also demonstrated that CcP can catalyze the oxidation of acrylonitrile, most likely to 2-cyanoethylene oxide in a “peroxygenase”-type reaction, with rates that are similar to rat liver microsomal cytochrome P450-catalyzed oxidation of acrylonitrile in the monooxygenase reaction. CcP compound I oxidizes acrylonitrile with a maximum turnover number of 0.61 min{sup −1} at pH 6.0.

  8. Characterization and development of new hydrogenated acrylonitrile-butadiene rubber blends

    Science.gov (United States)

    Severe, Geralda

    Characteristics were determined for hydrogenated acrylonitrile-butadiene rubber (HNBR), which is a copolymer of butadiene and acrylonitrile made from hydrogenation of the diene segment in acrylonitrile rubber. There was close attention given to the glass transition behavior of HNBR and its tendency to crystallize in the quiescent and in stretching state. The glass transition behavior in HNBR was similar to that of other ethylene copolymers such as for example ethylene vinyl-acetate etc. The crystallinity in HNBR at high acrylonitrile content was due to alternating sequence of acrylonitrile and hydrogenated trans-1,4 butadiene rubber. Furthermore, the structure of HNBR does not have any effect on it rheological properties at the temperature investigated. HNBR exhibits a zero shear viscosity. It is common knowledge that most polymers are immiscible. However, over the years scientists have found numerous miscible polymers. On that basis we investigated miscibility between HNBR with ethylenic copolymers, chlorinated polymers, diene polymers, and hydrogenated acrylonitrile-butadiene rubber. HNBR is miscible with high chlorine content chlorinated polymers like chlorinated polyethylene (42% Cl), chlorosulfonated polyethylene (43% Cl), PVC and CPVC. We have also developed dynamically vulcanized blends of HNBR with polychloroprene, epoxydized natural rubber, chlorobutyl, and carboxylated acrylonitrile-butadiene copolymer. Most of the blends at 75/25 composition have promising properties.

  9. Acrylonitrile is a multisite carcinogen in male and female B6C3F1 mice.

    Science.gov (United States)

    Ghanayem, Burhan I; Nyska, Abraham; Haseman, Joseph K; Bucher, John R

    2002-07-01

    Acrylonitrile is a heavily produced unsaturated nitrile, which is used in the production of synthetic fibers, plastics, resins, and rubber. Acrylonitrile is a multisite carcinogen in rats after exposure via gavage, drinking water, or inhalation. No carcinogenicity studies of acrylonitrile in a second animal species were available. The current studies were designed to assess the carcinogenicity of acrylonitrile in B6C3F1 mice of both sexes. Acrylonitrile was administered by gavage at 0, 2.5, 10, or 20 mg/kg/day, 5 days per week, for 2 years. Urinary thiocyanate and N-acetyl-S-(2-cyanoethyl)-L-cysteine were measured as markers of exposure to acrylonitrile. In general, there were dose-related increases in urinary thiocyanate and N-acetyl-S-(2-cyanoethyl)-L-cysteine concentrations in all dosed groups of mice and at all time points. Survival was significantly (p acrylonitrile-dosed groups. In female mice, the incidence of benign or malignant granulosa cell tumors (combined) in the ovary in the 10 mg/kg dose group was greater than that in the vehicle control group, but because of a lack of dose response, this was considered an equivocal finding. In addition, the incidences of atrophy and cysts in the ovary of the 10 and 20 mg/kg dose groups were significantly increased. The incidences of alveolar/bronchiolar adenoma or carcinoma (combined) were significantly increased in female mice treated with acrylonitrile at 10 mg/kg/day for 2 years. This was also considered an equivocal result. In conclusion, these studies demonstrated that acrylonitrile causes multiple carcinogenic effects after gavage administration to male and female B6C3F1 mice for 2 years.

  10. Synthesis, Characterization and Photophysical Properties of Pyridine-Carbazole Acrylonitrile Derivatives

    OpenAIRE

    Gabriel Ramos-Ortiz; Enrique Pérez-Gutiérrez; José Luis Maldonado; Chapela, Víctor M.; Margarita Cerón; M. Judith Percino

    2011-01-01

    We synthesized three novel highly fluorescent compounds, 2-(2’-pyridyl)-3-(N-ethyl-(3’-carbazolyl))acrylonitrile, 2-(3”-pyridyl)-3-(N-ethyl-(3’-carbazolyl))acrylonitrile, and 2-(4-pyridyl)-3-(N-ethyl-(3’-carbazolyl))acrylonitrile by Knoevenagel condensation. The first two were synthesized without solvent in the presence of piperidine as a catalyst; the third was synthesized without a catalyst and with N,N-dimethylformamide as a solvent. In solution, the molar absorption coefficients showed ab...

  11. In vivo comet assay of acrylonitrile, 9-aminoacridine hydrochloride monohydrate and ethanol in rats.

    Science.gov (United States)

    Nakagawa, Yuzuki; Toyoizumi, Tomoyasu; Sui, Hajime; Ohta, Ryo; Kumagai, Fumiaki; Usumi, Kenji; Saito, Yoshiaki; Yamakage, Kohji

    2015-07-01

    As part of the Japanese Center for the Validation of Alternative Methods (JaCVAM)-initiative international validation study of the in vivo rat alkaline comet assay, we examined the ability of acrylonitrile, 9-aminoacridine hydrochloride monohydrate (9-AA), and ethanol to induce DNA damage in the liver and glandular stomach of male rats. Acrylonitrile is a genotoxic carcinogen, 9-AA is a genotoxic non-carcinogen, and ethanol is a non-genotoxic carcinogen. Positive results were obtained in the liver cells of male rats treated with known genotoxic compounds, acrylonitrile and 9-AA.

  12. Hydration of acrylonitrile to produce acrylamide using biocatalyst in a membrane dispersion microreactor.

    Science.gov (United States)

    Li, Jiahui; Chen, Jie; Wang, Yujun; Luo, Guangsheng; Yu, Huimin

    2014-10-01

    In this work, a membrane dispersion microreactor was utilized for the hydration of acrylonitrile to produce acrylamide. Through observation using a microscopy, it was found that the acrylonitrile was dispersed into the continuous phase (the aqueous phase contains nitrile hydratase (NHase)) as droplets with a diameter ranged from 25 to 35 μm, hence the mass transfer specific surface area was significantly increased, and the concentration of acrylamide reached 52.5 wt% within 50 min. By contrast, in stirred tanks, the concentration of acrylamide only got 39.5 wt% within 245 min. Moreover, only a few amounts of acrylonitrile were accumulated in this microreactor system. Through optimizing the flow rate, the concentration of acrylamide reached 45.8 wt% within 35 min, the short reaction time greatly weakened the inhibition of acrylonitrile and acrylamide on the enzyme activity, which is suitable for prolonging the life of free cell.

  13. BARRIER PROPERTY AND STRUCTURE OF ACRYLONITRILE/ACRYLIC COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    YANG Zhenghua; LI Yuesheng

    1997-01-01

    A series of acrylonitrile (AN) copolymers with methyl acrylate (MA) or ethyl acrylate (EA) as comonomer (5-23 wt%) was prepared by free-radical copolymerization. The permeability coefficients of the copolymers to oxygen and carbon dioxide were measured at 1.0 MPa and at 30 ℃, and those to water vapor also measured at 100% relative humidity and at 30 ℃. All the AN/acrylic copolymers are semicrystalline. As the acrylate content increase, the permeability coefficients of the copolymers to oxygen and carbon dioxide are increased progressively, but those to water vapor are decreased progressively. The gas permeability coefficients of the polymers were correlated with free-volume fractions or the ratio of free volume to cohesive energy.

  14. Hydrolyzed Poly(acrylonitrile) Electrospun Ion-Exchange Fibers.

    Science.gov (United States)

    Jassal, Manisha; Bhowmick, Sankha; Sengupta, Sukalyan; Patra, Prabir K; Walker, Douglas I

    2014-06-01

    A potential ion-exchange material was developed from poly(acrylonitrile) fibers that were prepared by electrospinning followed by alkaline hydrolysis (to convert the nitrile group to the carboxylate functional group). Characterization studies performed on this material using X-ray photoelectron spectroscopy, scanning electron microscopy, Fourier-Transform infra-red spectroscopy, and ion chromatography confirmed the presence of ion-exchange functional group (carboxylate). Optimum hydrolysis conditions resulted in an ion-exchange capacity of 2.39 meq/g. Ion-exchange fibers were used in a packed-bed column to selectively remove heavy-metal cation from the background of a benign, competing cation at a much higher concentration. The material can be efficiently regenerated and used for multiple cycles of exhaustion and regeneration.

  15. A risk assessment for acrylonitrile in consumer products.

    Science.gov (United States)

    Johnston, P K; Rock, A R

    1990-12-15

    A carcinogenic risk assessment for acrylonitrile in consumer products was prepared as part of the Second Workshop on Pragmatics of Risk Assessment, Bethesda, MD. Data from one inhalation and two oral rat bioassays served as input into several high-to-low-dose mathematical risk extrapolation models. The final unit risk estimates for humans were based on maximum likelihood estimates from the Global83 implementation of the multistage model after adjustments for surface area differences, continuous versus intermittent exposures, and the proportion of lifetime exposed. The unit risk estimates for lifetime exposure to 1 mg kg-1 day-1 by inhalation and ingestion were 0.0531 and 0.2385, respectively. These risks are equivalent to risks of 3.3 x 10(-8) for inhalation of 1 ppt in air and 3.4 x 10(-9) for ingestion of 1 ng day.-1

  16. KINETIC STUDIES ON THE POLYMERIZATION OF ACRYLONITRILE INITIATED BY METALLIC MAGNESIUM-NITRIC ACID SYSTEM

    Institute of Scientific and Technical Information of China (English)

    WU Chinyung

    1983-01-01

    This article reports the polymerization kinetics of acrylonitrile initiated by metallic magnesiumnitric acid system. The rate of polymerization is independent of the amount of magnesium used; when the concentration of nitric acid is higher than acrylonitrile, the equation of polymerization kinetics may be expressed as Rp=1.91 × 105e-15000/RT[Mg]0 [AN]2·2 [HNO3]0·46 The result of copolymerization of acyrlonitrile and methyl acrylate supports a free-radical mechanism.

  17. Perinatal Toxicity and Carcinogenicity Studies of Styrene –Acrylonitrile Trimer, A Ground Water Contaminant

    OpenAIRE

    Behl, Mamta; Elmore, Susan A.; Malarkey, David E.; Hejtmancik, Milton R.; Gerken, Diane K.; Chhabra, Rajendra S.

    2013-01-01

    Styrene Acrylonitrile (SAN) Trimer is a by-product in the production of acrylonitrile styrene plastics. Following a report of a childhood cancer cluster in the Toms River section of Dover Township, New Jersey, SAN Trimer was identified as one of the groundwater contaminants at Reich Farm Superfund site in the township. The contaminants from the Reich Farm site’s ground water plume impacted two wells at the Parkway well field. The National Toxicology Program (NTP) studied the toxicity and carc...

  18. EFFECTS OF SOLVENT POLARITY ON FREE RADICAL COPOLY MERIZATION OF 5-HEXENOIC ACID AND ACRYLONITRILE

    Institute of Scientific and Technical Information of China (English)

    WANG Bing; XIE Shishan; CAO Mengjiun

    1987-01-01

    The effects of solvent polarity on free radical copolymerization of 5-hexenoic acid and acrylonitrile at 60℃ were studied. It was observed that as the polarity of solvents enhanced, both the copolymerization rate and the reactivity ratios r1, r2 increased, while the alternating tendency of monomer units in copolymer chain decreased. It is believed that the solvent polarity raises the reactivities of acrylonitrile monomer and its growing chain radical, but causes no distinct variation in those of 5-hexenoic acid.

  19. Grafting of acrylonitrile onto cellulosic material derived from bamboo (Dendrocalamus strictus

    Directory of Open Access Journals (Sweden)

    2008-01-01

    Full Text Available Bamboo, a lignocellulosic biopolymer material, is of interest as feedstock for production of cellulose derivatives by chemical functionalization. Optimization of grafting of acrylonitrile onto cellulosic material (average Degree of Polymerization 816, isolated from bamboo (Dendrocalamus stictus was performed by varying the process parameters such as duration of soaking of cellulosic material in ceric ammonium nitrate solution, ceric ammonium nitrate concentration, polymerization time, temperature of reaction and acrylonitrile concentration to study their influence on percent grafting and grafting efficiency. Graft copolymerization of acrylonitrile onto cellulosic material derived from bamboo (Dendrocalamus strictus in heterogenous medium can be initiated effectively with ceric ammonium nitrate. The optimum reaction conditions obtained for grafting of acrylonitrile onto cellulosic material were: duration of dipping cellulosic material in ceric ammonium nitrate solution 1 hr, ceric ammonium nitrate concentration 0.02 M, acrylonitrile concentration 24.6 mol/anhydroglucose unit, temperature of reaction 40°C and polymerization time 4 hrs. The percent grafting for optimized samples is 210.3% and grafting efficiency is 97%. The characterization of the grafted products by means of FTIR and Scanning Electron Microscopy furnished the evidence of grafting of acrylonitrile onto the cellulosic material.

  20. The Formation and characteristics of Acrylonitrile/Urea Inclusion Compound

    CERN Document Server

    Zou, Jun-Ting; Pang, Wen-Min; Shi, Lei; Lu, Fei

    2012-01-01

    The formation process and composition of the acrylonitrile/urea inclusion compounds (AN/UIC) with different aging times and AN/urea molar feed ratios are studied by differential scanning calorimetry (DSC) and X-ray diffraction (XRD). It is suggested that DSC could be one of the helpful methods to determine the guest/host ratio and the heat of decomposition. Meanwhile, the guest/host ratio and heat of deformation are obtained, which are 1.17 and 5361.53 J/mol, respectively. It is found that the formation of AN/UIC depends on the aging time. The formation process ends after enough aging time and the composition of AN/UIC becomes stable. It is suggested AN molecules included in urea canal lattice may be packed flat against each other. XRD results reveal that once AN molecules enter urea lattice, AN/UIC are formed, which possess the final structure. When AN molecules are sufficient, the content of AN/UIC increased as aging time prolonging until urea tunnels are saturated by AN.

  1. Recycling of Chrome Tanned Leather Dust in Acrylonitrile Butadiene Rubber

    Science.gov (United States)

    El-Sabbagh, Salwa H.; Mohamed, Ola A.

    2010-06-01

    Concerns on environmental waste problem caused by chrome tanned leather wastes in huge amount have caused an increasing interest in developing this wastes in many composite formation. This leather dust was used as filler in acrylonitrile butadiene rubber (NBR) before treatment and after treatment with ammonia solution and sod. formate. Different formulations of NBR/ leather dust (untreated-treated with ammonia solution—treated with sod. formate) composites are prepared. The formed composite exhibit a considerable improvement in some of their properties such as rheometric characteristics especially with composites loaded with treated leather dust. Tensile strength, modulus at 100% elongation, hardness and youngs modulus were improved then by further loading start to be steady or decrease. Cross linking density in toluene were increased by incorporation of leather dust treated or untreated resulting in decreases in equilibrium swelling. Distinct increase in the ageing coefficient of both treated and untreated leather with drop in NBR vulcanizates without leather dust. Addition of leather dust treated or untreated exhibit better thermal stability.

  2. Lactoperoxidase catalyzes in vitro activation of acrylonitrile to cyanide.

    Science.gov (United States)

    Nasralla, Sherry N; Ghoneim, Asser I; Khalifa, Amani E; Gad, Mohamed Z; Abdel-Naim, Ashraf B

    2009-12-15

    Acrylonitrile (ACN) is a widely used industrial chemical. Although it is a well reported animal carcinogen, its current designation to humans is "possibly carcinogenic". The present study aimed at investigating the ability of LPO enzyme system to oxidize ACN to cyanide (CN(-)) in vitro. Detection of CN(-) served as a marker for the possible generation of free radical intermediates implicated in ACN induced toxicity in the activation process. Optimum conditions for the oxidation of ACN to CN(-) were characterized with respect to pH, temperature and time of incubation as well as ACN, LPO and H(2)O(2) concentrations in incubation mixtures. Maximum reaction velocity (V(max)) and Michaelis-Menten constant (K(m)) were assessed. Addition of nitrite (NO(2)(-)) salts to the reaction mixtures significantly enhanced the rate of the reaction. Free radical scavengers (quercetin and trolox C), LPO enzyme inhibitor (resorcinol) and competitors for LPO binding (sodium azide and indomethacin) were found to reduce the rate of CN(-) production. Inclusion of the sulfhydryl compounds glutathione (GSH), NAC (N-acetylcysteine), D-penicillamine or L-cysteine enhanced the rate of ACN oxidation. The present results demonstrate the ability of LPO enzyme system to oxidize ACN to CN(-) and provide insight for the elucidation of ACN chronic toxicity.

  3. Assessment of risk from exposure to acrylonitrile: the general approach used by a consultant.

    Science.gov (United States)

    Page, N P; Cook, B

    1990-12-15

    The concern from low-level exposure to acrylonitrile is primarily due to its potential for carcinogenicity. Several epidemiology studies provide suggestive evidence for an association of lung cancer in workers exposed to acrylonitrile; however, smoking may be a contributing factor and therefore the role of acrylonitrile as a causative factor is unclear. Seven animal bioassays, using three routes of exposure and two strains of rats, have provided consistent results. Tumors were induced in all studies, with the primary sites of tumor induction being the brain, ear canal, gastrointestinal tract and mammary glands. The linearized multistage model was used for extrapolation purposes. The risk based on brain tumors (astrocytomas) and stomach tumors following oral exposures ranged from 1 x 10(-1) to 4 x 10(-1)mg-1kg-1day-1. The risk of inhalation exposure is somewhat less, (2-3) x 10(-2). Support for carcinogenic potential is obtained from mutagenicity studies. Acrylonitrile has been found to be mutagenic and also binds with DNA. It has been speculated that acrylonitrile is metabolized to 2-cyanoethylene oxide, which is the proximate carcinogen.

  4. Pre-irradiation induced emulsion graft polymerization of acrylonitrile onto polyethylene nonwoven fabric

    Science.gov (United States)

    Liu, Hanzhou; Yu, Ming; Deng, Bo; Li, Linfan; Jiang, Haiqing; Li, Jingye

    2012-01-01

    Acrylonitrile has been widely used in the modification of polymers by graft polymerization. In the present work, pre-irradiation induced emulsion graft polymerization method is used to introduce acrylonitrile onto PE nonwoven fabric instead of the traditional reaction in organic solvents system. The degree of grafting (DG) is measured by gravimetric method and the kinetics of the graft polymerization is studied. The existence of the graft chains is proven by Fourier transform infrared spectroscopy (FT-IR) analysis. Thermal stability of the grafted polymer is measured by Thermogravimetric analysis (TGA).

  5. KINETICS OF POLYMERIZATION OF ACRYLONITRILE INITIATED BY VANADIUM(V) - THIOUREA REDOX SYSTEM

    Institute of Scientific and Technical Information of China (English)

    WU Jinyuan; YANG Chaoxiong; WU Yuxian

    1990-01-01

    The kinetics of polymerization of acrylonitrile (AN) initiated by quinquevalent vanadium (V5+ )-thiourea (TU) redox system has been investigated in aqueous nitric acid in the temperature range from 30 to 50 ℃ . The polymerization rate (Rp) can be expressed as follows:Rp= 2.80×105e- 14,200/RT[AN] 2,2[V5+] 0~1/3[TU] 0~4/3[HNO3] 0.2. In the copolymerization of acrylonitrile with methyl acrylate (MA), the reactivity ratios were found to be 1.0 and 1.1, respectively. The experimental observations suggest that the initiating species is probably a complex consisting of a central ion of Lewis acid-VO+2 and the ligands of Lewis bases-acrylonitrile, thiourea, and nitrate anions, while the initiating system in lower concentration, the polymerization of acrylonitrile does not occur if the thiourea is acidified prior to its reaction with quinquevalent vanadium. This indicates that the primary radicals (or the monomeric radicals in the present article) are produced by associated thiourea rather than isothiourea.

  6. Arylation of Acrylamide and Acrylonitrile with Arenediazonium Salts Catalyzed by Palladium Acetate

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Arylation of acrylamide and acrylonitrile were carried out with various arenediazonium tetrafluoroborates in the presence of a catalytic amount of Pd(OAc)2 in ethanol and a variety of substituted (E)-cinnamamides and (E)-cinnamonitriles were obtained in high yields under mild reaction conditions.

  7. Genotoxicity of Styrene–Acrylonitrile Trimer in Brain, Liver, and Blood Cells of Weanling F344 Rats

    OpenAIRE

    Hobbs, Cheryl A.; Chhabra, Rajendra S.; Recio, Leslie; Streicker, Michael; Witt, Kristine L.

    2012-01-01

    Styrene–acrylonitrile Trimer (SAN Trimer), a by-product in production of acrylonitrile styrene plastics, was identified at a Superfund site in Dover Township, NJ, where childhood cancer incidence rates were elevated for a period of several years. SAN Trimer was therefore tested by the National Toxicology Program in a 2-year perinatal carcinogenicity study in F344/N rats and a bacterial mutagenicity assay; both studies gave negative results. To further characterize its genotoxicity, SAN Trimer...

  8. Dimedone-catalyzed Addition of Amines into Cyano Group: Facile Synthesis of Thiazol-2-yl Substituted E-Acrylonitriles

    Institute of Scientific and Technical Information of China (English)

    朱伟军; 屠兴超; 冯惠; 屠蔓苏; 姜波; 吴飞跃; 屠树江

    2012-01-01

    An efficient dimedone-catalyzed synthesis of highly functionalized thiazol-2-yl substituted E-acrylonitrile derivatives has been established through two-step reaction of a-thiocyanate ketones with malononitrile and amines. The a-thiocyanate ketones were subjected with malononitrile to provide thiazol-2-ylidenemalononitrile derivatives, followed with various amines in the presence of dimedone to yield the final thiazol-2-yl substituted acrylonitrile derivatives.

  9. Nitrilase-catalysed conversion of acrylonitrile by free and immobilized cells of Streptomyces sp.

    Indian Academy of Sciences (India)

    V K Nigam; A K Khandelwal; R K Gothwal; M K Mohan; B Choudhury; A S Vidyarthi; P Ghosh

    2009-03-01

    The biotransformation of acrylonitrile was investigated using thermophilic nitrilase produced from a new isolate Streptomyces sp. MTCC 7546 in both the free and immobilized state. Under optimal conditions, the enzyme converts nitriles to acids without the formation of amides. The whole cells of the isolate were immobilized in agar-agar and the beads so formed were evaluated for 25 cycles at 50°C. The enzyme showed a little loss of activity during reuse. Seventy-one per cent of 0.5 M acrylonitrile was converted to acid at 6 h of incubation at a very low density of immobilized cells, while 100% conversion was observed at 3 h by free cells.

  10. Detection of acrolein and acrylonitrile with a pulsed room temperature quantum cascade laser

    Science.gov (United States)

    Manne, J.; Jäger, W.; Tulip, J.

    2010-06-01

    We investigated the use of a pulsed, distributed feedback quantum cascade laser centered at 957 cm-1 in combination with an astigmatic Herriot cell with 250 m path length for the detection of acrolein and acrylonitrile. These molecules have been identified as hazardous air-pollutants because of their adverse health effects. The spectrometer utilizes the intra-pulse method, where a linear frequency down-chirp, that is induced when a top-hat current pulse is applied to the laser, is used for sweeping across the absorption line. Up to 450 ns long pulses were used for these measurements which resulted in a spectral window of ~2.2 cm-1. A room temperature mercury-cadmium-telluride detector was used, resulting in a completely cryogen free spectrometer. We demonstrated detection limits of ~3 ppb for acrylonitrile and ~6 ppb for acrolein with ~10 s averaging time. Laser characterization and optimization of the operational parameters for sensitivity improvement are discussed.

  11. Bioconversion of acrylonitrile to acrylamide using polyacrylamide entrapped cells of Rhodococcus rhodochrous PA-34.

    Science.gov (United States)

    Raj, J; Prasad, S; Sharma, N N; Bhalla, T C

    2010-09-01

    The nitrile hydratase (NHase) of Rhodococcus rhodochrous PA-34 catalyzed the conversion of acrylonitrile to acrylamide. The resting cells (having NHase activity) (8 %; 1 mL corresponds to 22 mg dry cell mass, DCM) were immobilized in polyacrylamide gel containing 12.5 % acrylamide, 0.6 % bisacrylamide, 0.2 % diammonium persulfate and 0.4 % TEMED. The polyacrylamide entrapped cells (1.12 mg DCM/mL) completely converted acrylonitrile in 3 h at 10 °C, using 0.1 mol/L potassium phosphate buffer. In a partitioned fed batch reactor, 432 g/L acrylamide was accumulated after 1 d. The polyacrylamide discs were recycled up to 3×; 405, 210 and 170 g/L acrylamide was produced in 1st, 2nd and 3rd recycling reactions. In four cycles, a total of 1217 g acrylamide was produced by recycling the same mass of entrapped cells.

  12. Urinary excretion of the acrylonitrile metabolite 2-cyanoethylmercapturic acid is correlated with a variety of biomarkers of tobacco smoke exposure and consumption

    Science.gov (United States)

    Minet, Emmanuel; Cheung, Francis; Errington, Graham; Sterz, Katharina; Scherer, Gerhard

    2011-01-01

    Acrylonitrile is an IARC class 2B carcinogen present in cigarette smoke. Urinary 2-cyanoethylmercapturic acid (CEMA) is an acrylonitrile metabolite and a potential biomarker for acrylonitrile exposure. The objective of this work was to study the dose response of CEMA in urine of non-smokers and smokers of different ISO tar yield cigarettes. We observed that smokers excreted >100-fold higher amounts of urinary CEMA than non-smokers. The CEMA levels in smokers were significantly correlated with ISO tar yield, daily cigarette consumption, and urinary biomarkers of smoke exposure. In conclusion, urinary CEMA is a suitable biomarker for assessing smoking-related exposure to acrylonitrile. PMID:21108560

  13. Urinary excretion of the acrylonitrile metabolite 2-cyanoethylmercapturic acid is correlated with a variety of biomarkers of tobacco smoke exposure and consumption.

    Science.gov (United States)

    Minet, Emmanuel; Cheung, Francis; Errington, Graham; Sterz, Katharina; Scherer, Gerhard

    2011-02-01

    Acrylonitrile is an IARC class 2B carcinogen present in cigarette smoke. Urinary 2-cyanoethylmercapturic acid (CEMA) is an acrylonitrile metabolite and a potential biomarker for acrylonitrile exposure. The objective of this work was to study the dose response of CEMA in urine of non-smokers and smokers of different ISO tar yield cigarettes. We observed that smokers excreted >100-fold higher amounts of urinary CEMA than non-smokers. The CEMA levels in smokers were significantly correlated with ISO tar yield, daily cigarette consumption, and urinary biomarkers of smoke exposure. In conclusion, urinary CEMA is a suitable biomarker for assessing smoking-related exposure to acrylonitrile.

  14. Design and Testing of Digitally Manufactured Paraffin Acrylonitrile-Butadiene-Styrene Hybrid Rocket Motors

    OpenAIRE

    McCulley, Jonathan M.

    2013-01-01

    This research investigates the application of additive manufacturing techniques for fabricating hybrid rocket fuel grains composed of porous Acrylonitrile-butadiene-styrene impregnated with paraffin wax. The digitally manufactured ABS substrate provides mechanical support for the paraffin fuel material and serves as an additional fuel component. The embedded paraffin provides an enhanced fuel regression rate while having no detrimental effect on the thermodynamic burn properties of the fuel g...

  15. Innovative Application of Biopolymer Keratin as a Filler of Synthetic Acrylonitrile-Butadiene Rubber NBR

    OpenAIRE

    Mirosława Prochoń; Anita Przepiórkowska

    2013-01-01

    The current investigations show the influence of keratin, recovered from the tanning industry, on the thermal and mechanical properties of vulcanizates with synthetic rubber acrylonitrile-butadiene rubber NBR. The addition of waste protein to NBR vulcanizates influences the improvement of resistance at high temperatures and mechanical properties like tensile strength and hardness. The introduction of keratin to the mixes of rubber previously blended with zinc oxide (ZnO) before vulcanization ...

  16. Screening-Level Risk Assessment for Styrene-Acrylonitrile (SAN) Trimer Detected in Soil and Groundwater

    OpenAIRE

    Kirman, C. R.; Gargas, M L; Collins, J. J.; Rowlands, J. C.

    2012-01-01

    A screening-level risk assessment was conducted for styrene-acrylonitrile (SAN) Trimer detected at the Reich Farm Superfund site in Toms River, NJ. Consistent with a screening-level approach, on-site and off-site exposure scenarios were evaluated using assumptions that are expected to overestimate actual exposures and hazards at the site. Environmental sampling data collected for soil and groundwater were used to estimate exposure point concentrations. Several exposure scenarios were evaluate...

  17. Synthesis, Characterization and Photophysical Properties of Pyridine-Carbazole Acrylonitrile Derivatives

    OpenAIRE

    Pérez-Gutiérrez,Enrique; Percino, M. Judith; Chapela, Víctor M.; Cerón, Margarita; Maldonado, José Luis; Ramos-Ortiz, Gabriel

    2011-01-01

    in solid state, absorptions were at 398, 390, and 442 nm, respectively. The fluorescence emission was at 540, 540 and 604 nm, respectively, the 2-(4-pyridyl)-3-(N-ethyl-(3’-carbazolyl))acrylonitrile showed a red shift in the emission of 64 nm compared to the other two compounds. The fluorescence quantum yield for the compounds in powder form showed values of 0.05, 0.14, and 0.006, respectively

  18. STUDY ON THE EPOXY RESIN TOUGHENED BY HYDROXY-TERMINATED BUTADIENE-ACRYLONITRILE COPOLYMER

    Institute of Scientific and Technical Information of China (English)

    HAN Xiaozu; LI Shaoying; ZHANG Qingyu

    1990-01-01

    Toughened epoxy resin with excellent properties was obtained by adding organic acid anhydride curing agent and hydroxy-terminated butadiene-acrylonitrile copolymer (HTBN), which is cheaper than CTBN. The anhydride reacts with both epoxy groups on epoxy resin and hydroxyl groups on HTBN. As a result the soft long chains of HTBN and the rigid chain of epoxy resin form one network, giving the resin toughness. Two-phase structure of the toughened resin was observed by SEM and TEM.

  19. Sorption studies on Cr (VI) removal from aqueous solution using cellulose grafted with acrylonitrile monomer.

    Science.gov (United States)

    Hajeeth, T; Sudha, P N; Vijayalakshmi, K; Gomathi, T

    2014-05-01

    Graft copolymerization of acrylonitrile on to cellulosic material derived from sisal fiber can be initiated effectively with ceric ammonium nitrate. The grafting conditions were optimized by changing the concentration of initiator and monomer. The change in crystallinity of the grafted polymeric samples was concluded from the XRD patterns. The prepared cellulose grafted acrylonitrile copolymer was used as an adsorbent to remove Cr (VI) ions from aqueous solutions. The efficiency of the adsorbent was identified from the variation in the percentage of adsorption with contact time, adsorbent dose and pH. From the observed results it was evident that the adsorption of metal ions increases with the increase in contact time and metal ion concentration. An optimum pH was found to be 5.0 for the removal of Cr (VI) from the aqueous solution. The results of the Langmuir, Freundlich, and pseudo first- and second-order studies revealed that the adsorption was found to fit well with Freundlich isotherm and follows pseudo second-order kinetics. From the above results, it was concluded that the cellulose-g-acrylonitrile copolymer was found to be an efficient adsorbent for the removal of Cr (VI) from aqueous waste generated from industries.

  20. Electromechanical responses of poly(3-thiopheneacetic acid/acrylonitrile-butadiene rubbers

    Directory of Open Access Journals (Sweden)

    2008-12-01

    Full Text Available Acrylonitrile-butadiene rubber (NBR and blends of poly(3-thiopheneacetic acid/ acrylonitrile-butadiene rubber, P3TAA/NBR, were fabricated, and the electrorheological properties, dielectric, and electrical conductivities were investigated . The electrorheological properties were determined under an oscillatory shear mode in a frequency range of 0.1 to 100 rad/s at various electric field strengths, from 0 to 2 kV/mm, at a fixed 27°C to observe the effects of acrylonitrile content (ACN in the rubber systems and the conductive particle concentration in the blends. For the pure rubber systems, the storage modulus response (ΔG′ is linearly dependent on its dielectric constant (ε′, and increases with the ACN content. For the NBR/P3TAA blends, the storage modulus response varies nonlinearly with the dielectric constant. The bending responses of the rubbers and the blends were investigated in a vertical cantilever fixture. For the pure rubber system, the bending angle and the dielectrophoresis force vary linearly with electric field strength. For the blend system, the bending angle and the dielectrophoresis force vary nonlinearly with electric field strength.

  1. Adsorption of Acrylonitrile on Some Soils and Minerals from Aqueous Solutions

    Institute of Scientific and Technical Information of China (English)

    WUDE-YI; N.MATSUE; 等

    1993-01-01

    Equilibrium and kinetic studies have been made on the adsorption of acrylonitrile(CH2=CHCN) on three soils and four minerals from aqueous solutions.It was shown that the organic matter was the major factor affecting the adsorption process in the soils.The conformity of the equilibrium data to linear type(one soil) and Langmuir type(two soils) isotherms indicated that different mechanisms were involved in the adsorption.This behavior appears bo be related to the hydrophobicity of soil organic matter due to their composition and E4/E6 ratio of humic acids.The adsorption kinetics were also different among the soils,indicating the difference in porosity of organic matter among the soils,and the kinetics strongly affected the adsorption capacity of soils for acrylonitrile.Acrylonitrile was slightly adsorbed from aqueous solutions on pyrophyllite with electrically neutral and hydrophobic nature,and practically not on montmorillonite and kaolinite saturated with Ca.However,much higher adsorption occurred on the zeolitized coal ash,probably caused by high organic carbon content(107g/kg).

  2. Estimation of the Surface Properties of Styrene-Acrylonitrile Random Copolymers from Contact Angle Measurements.

    Science.gov (United States)

    Adão; Saramago; Fernandes

    1999-09-01

    The surface free energy per unit area of a solid, gamma(S), is a fundamental property of materials and determines their surface and interfacial behavior in processes like wetting and adhesion. In this study the gamma(S) of a series of styrene-acrylonitrile random copolymers is evaluated. Three different approaches are used to determine the components in which the surface free energy can be decomposed. Using the geometric and the harmonic mean approach, the dispersive, gamma(d), and polar, gamma(p), components of the solid surface free energy were determined and compared to the Lifshitz-van der Waals, gamma(LW), and acid-base, gamma(AB), components using the approach developed by C. J. van Oss et al. (1987, Adv. Colloid Interface Sci. 28, 35). The acid-base approach was also used to evaluate the work of adhesion of the test liquids: water, glycerol, and thiodiglycol. It was found that the contact angles of these liquids follow closely the predictions of Cassie equation. The evaluation of the surface free energy components on one hand and the relative magnitude of the work of adhesion components on the other hand, suggest that below 50% of acrylonitrile the polystyrene repeating units are preferentially at the surface. Above 50% of acrylonitrile the segregation of the low-energy homopolymer at the surface decreases. Copyright 1999 Academic Press.

  3. Stepwise mechanism of oxidative ammonolysis of propane to acrylonitrile over gallium-antimony oxide catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Osipova, Z.G.; Sokolovskii, V.D.

    1979-03-01

    The stepwise mechanism of oxidative ammonolysis of propane to acrylonitrile over gallium-antimony oxide catalysts GaSb/sub 19/O/sub x/, GaSb/sub 3/Ni/sub 1.5/0/sub x/, and GaSb/sub 2.5/Ni/sub 1.5/PW/sub 0//sub 0.25/O/sub x/ was studied at 450/sup 0/ and 550/sup 0/C by introducing alternating pulses of 0.5Vertical Bar3< propane/0.6Vertical Bar3< ammonia/helium (to reduce the steady-state catalytic surface) and 0.5Vertical Bar3< propane/0.6Vertical Bar3< ammonia/1.86Vertical Bar3< oxygen/helium mixtures into a fluidized-bed catalytic reactor. Over all the catalysts studied, the rates of acrylonitrile formation during the two types of pulses were very similar, but carbon dioxide was formed much faster during the reducing pulses, particularly at 450/sup 0/C. These findings suggested that acrylonitrile is formed by a stepwise redox mechanism involving consecutive interaction of propane and ammonia with the surface oxygen of the catalysts and oxidation of the reduced catalyst surface by gas-phase oxygen. The formation of carbon dioxide proceeds by both stepwise and associative mechanisms, the latter being more important at higher temperatures. The results are similar to published results for ammoxidation of propylene and olefins.

  4. STUDY ON POLYMERIC CATALYST—PALLADIUM COMPLEX WITH RADIATION GRAFTING ACRYLONITRILE ON INORGANIC COMPOUND

    Institute of Scientific and Technical Information of China (English)

    ZHANGWanxi; CHEJitai

    1993-01-01

    Polymer bound palladium (Pd) complex catalysts with grafting acrylonitrile on inorganic compound(MgO,Y-molecular sieve and SiO2) by pre-radiation method were studies.The palladium-grafting polymers have been investigated by X-ray photoelectron spectrscopy(XPS).It is indicated that peak width of C1s and O1s spectra of MgO-g-PAN-Pd(radiation-induced graft) is wider than that of MgO-PAN-Pd(chemical method) and Peak numbers of former are one more than later.According to the report in reference,this peak is attributed to -O-C group.Thus,the graft acrylonitrile on MgO may complete through oxygen atoms im MgO and β-carbon atoms in acrylonitrile.The polymer catalyst obtained by radiation grafting is a higher active hydrogenation catalyst for olefines and better antioxic than that of one obtained by chemical method,and it has selectivity for hydrogenation catalyst.

  5. Characterisation of recycled acrylonitrile-butadiene-styrene and high-impact polystyrene from waste computer equipment in Brazil.

    Science.gov (United States)

    Hirayama, Denise; Saron, Clodoaldo

    2015-06-01

    Polymeric materials constitute a considerable fraction of waste computer equipment and polymers acrylonitrile-butadiene-styrene and high-impact polystyrene are the main thermoplastic polymeric components found in waste computer equipment. Identification, separation and characterisation of additives present in acrylonitrile-butadiene-styrene and high-impact polystyrene are fundamental procedures to mechanical recycling of these polymers. The aim of this study was to evaluate the methods for identification of acrylonitrile-butadiene-styrene and high-impact polystyrene from waste computer equipment in Brazil, as well as their potential for mechanical recycling. The imprecise utilisation of symbols for identification of the polymers and the presence of additives containing toxic elements in determinate computer devices are some of the difficulties found for recycling of acrylonitrile-butadiene-styrene and high-impact polystyrene from waste computer equipment. However, the considerable performance of mechanical properties of the recycled acrylonitrile-butadiene-styrene and high-impact polystyrene when compared with the virgin materials confirms the potential for mechanical recycling of these polymers.

  6. Control of insects with fumigants at low temperatures: toxicity of mixtures of methyl bromide and acrylonitrile to three species of insects

    Energy Technology Data Exchange (ETDEWEB)

    Bond, E.J.; Buckland, C.T.

    1976-12-15

    Acrylonitrile can be mixed with methyl bromide to increase toxicity so that the quantity of methyl bromide required for control of Sitophilus granarius (L.), Tenebrio molitor L., and Tribolium confusum Jacquelin duval is reduced by one half. Mixtures of methyl bromide and acrylonitrile are considerably more effective at low temperatures than methyl bromide alone.

  7. STUDIES ON THE POLYMERIZATION OF ACRYLONITRILE INITIATED BY METAVANADATE- CONTAINING ANION EXCHANGER-THIOUREA REDOX SYSTEM

    Institute of Scientific and Technical Information of China (English)

    YANG Chaoxiong; WU Jinyuan; WU Yuxian

    1991-01-01

    The polymerization of acrylonitrile (AN) in aqueous nitric acid initiated by metavanadate-containing anion exchange resin (PV)-thiourea (TU) redox system at 20- 40 ℃. has been investigated. The overall rate of polymerization (Rp) is given by Rp= 1.92 × 104 e -6,860/RT [AN]1.2[PV]0.44[TU]1.0[HNO3]1.0 The kinetic parameters differed from those of V5+-TU system indicated that the generation of the primary radicals is mainly a difffusion-controlled reaction . The effect of macromolecular field arisen from the polymer matrix exerts a great influence on the polymerization process.

  8. DEPENDENCE OF ACRYLONITRILE POLYMERIZATION KINETICS ON THE COMPOSITION OF POLYAMID OXIME -THIOUREA SYSTEM

    Institute of Scientific and Technical Information of China (English)

    WU Jinyuan; YANG Chaoxiong; ZHANG Guangzhao

    1993-01-01

    The polymerization of acrylonitrile (AN) initiated by polypropylene based-polyamidoxime (PPAO)- thiourea (TU) system was investigated at [ TU]/[ PPAO] > 0.5 molar ratio. It shows that the variation of the concentrations of PPAO, thiourea and nitric acid does not exert an observable influence on the reaction rate. The overall rate of polymerization (Rp) is Rp = 2.07e - 7,800/RT[AN] 2.0The zero order dependence on PPAO and thiourea concentrations and the lowest value of the collision frequence factor were considered to be a feature of the primary radical termination.

  9. Mechanical properties of products of thermocatalytic and radiolytic styrene - acrylonitrile copolymerization

    Energy Technology Data Exchange (ETDEWEB)

    Gadalla, A.M.; Derini, M.A.E.

    1983-12-01

    The mechanical properties of styrene (S)-acrylonitrile (AN) mixtures, ranging from 20 to 80 wt % S, polymerized by thermocatalytic and radiolytic techniques were studied. Maximum compressive and tensile strength was obtained for the mixture containing 60 wt % styrene. The hardness increased with styrene concentration up to 40 wt % and then remained nearly constant. Radiolytic copolymerization gave stronger copolymers than thermal copolymerization since irradiation enhances crosslinking. For the same composition, as the dose increases, the strength increases to a maximum and then decreases due to competing rates of crosslinking and degradation. 5 figures.

  10. ION CONDUCTION IN COMPLEX OF ACRYLONITRILE-COPOLYMERIZED COMB POLYETHER WITH LITHIUM PERCHLORATE

    Institute of Scientific and Technical Information of China (English)

    XU Kang; DENG Zhenghua; WAN Guoxiang

    1991-01-01

    Poly ( oligoether methacrylate- co- acrylonitrile ) s, P ( MEOn- AN ), with oligoether pendants of different lengths were synthesized and the ion conduction property of their Li-salt complexes was studied as the function of polymer structure. At proper copolymer composition, lithium concentration and pendant length, the ion conductivity reaches 7.0×10-5S/cm at ambient temperature, together with improved mechanical strength. The ion transport in the polymer media is assisted by segmental relaxation ,which is confirmed both by the consistency between ion conductivity and Tg and by the study of TSC.

  11. Adsorptive removal of acrylonitrile by commercial grade activated carbon: kinetics, equilibrium and thermodynamics.

    Science.gov (United States)

    Kumar, Arvind; Prasad, B; Mishra, I M

    2008-04-01

    The potential of activated carbons--powdered (PAC) and granular (GAC), for the adsorption of acrylonitrile (AN) at different initial AN concentrations (50PAC and GAC, respectively. Error analysis also confirmed the efficacy of the R-P isotherm to best fit the experimental data. The pseudo-second order kinetic model best represents the kinetics of the adsorption of AN onto PAC and GAC. Maximum adsorption capacity of PAC and GAC at optimum conditions of AN removal (adsorbent dose approximately 20 g/l of solution, and equilibrium time approximately 5 h) was found to be 51.72 and 46.63 mg/g, respectively.

  12. Theoretical study on the gas phase reaction of acrylonitrile with a hydroxyl radical.

    Science.gov (United States)

    Sun, Jingyu; Wang, Rongshun; Wang, Baoshan

    2011-10-01

    The mechanism and kinetics of the reaction of acrylonitrile (CH(2)=CHCN) with hydroxyl (OH) has been investigated theoretically. This reaction is revealed to be one of the most significant loss processes of acrylonitrile. BHandHLYP and M05-2X methods are employed to obtain initial geometries. The reaction mechanism conforms that OH addition to C[double bond, length as m-dash]C double bond or C atom of -CN group to form the chemically activated adducts, 1-IM1(HOCH(2)=CHCN), 2-IM1(CH(2)=HOCHCN), and 3-IM1(CH(2)=CHCOHN) via low barriers, and direct hydrogen abstraction paths may also occur. Temperature- and pressure-dependent rate constants have been evaluated using the Rice-Ramsperger-Kassel-Marcus theory. The calculated rate constants are in good agreement with the experimental data. At atmospheric pressure with N(2) as bath gas, 1-IM1(OHCH(2)=CHCN) formed by collisional stabilization is the major product in the temperature range of 200-1200 K. The production of CH(2)CCN and CHCHCN via hydrogen abstractions becomes dominant at high temperatures (1200-3000 K).

  13. Acrylonitrile-methyl Methacrylate Copolymer Films Containing Microencapsulated n-Octadecane

    Institute of Scientific and Technical Information of China (English)

    LI Jun; HAN Na; ZHANG Xing-xiang

    2006-01-01

    Acrylonitrile-methyl methacrylate copolymer was synthesized in aqueous solution by Redox. The copolymer was mixed with 10 - 40 wt% of microencapsulated n-octadecane (MicroPCMs) in water. Copolymer films containing MicroPCMs were cast at room temperature in N, N-Dimethylformamide solution. The copolymer of acrylonitrile-methyl methacrylate and the copolymer films containing MicroPCMs were characterized by using Fourier Transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC), Thermogravimetric Analyzer (TG), X-ray Diffrac tion (XRD) and Scanning Electron Microscopy (SEM), etc.The microcapsules in the films are evenly distributed in the copolymer matrix. The heat-absorbing temperatures and heat-evolving temperatures of the films are almost the same as that of the MicroPCMs, respectively, and fluctuate in a slight range. In addition, the enthalpy efficiency of MicroPCMs rises with the contents of MicroPCMs increasing.The crystallinity of the film increases with the contents of MicroPCMs increasing.

  14. Sensitive detection of acrolein and acrylonitrile with a pulsed quantum-cascade laser

    Science.gov (United States)

    Manne, J.; Lim, A.; Tulip, J.; Jäger, W.

    2012-05-01

    We report on spectroscopic measurements of acrolein and acrylonitrile at atmospheric pressure using a pulsed distributed feedback quantum-cascade laser in combination with intra- and inter-pulse techniques and compare the results. The measurements were done in the frequency region around 957 cm-1. In the inter-pulse technique, the laser is excited with short current pulses (5-10 ns), and the pulse amplitude is modulated with an external current ramp resulting in a ˜2.3 cm-1 frequency scan. In the intra-pulse technique, a linear frequency down-chirp during the pulse is used for sweeping across the absorption line. Long current pulses up to 500 ns were used for these measurements which resulted in a spectral window of ˜2.2 cm-1 during the down-chirp. These comparatively wide spectral windows facilitated the measurements of the relatively broad absorption lines (˜1 cm-1) of acrolein and acrylonitrile. The use of a room-temperature mercury-cadmium-telluride detector resulted in a completely cryogen-free spectrometer. We demonstrate ppb level detection limits within a data acquisition time of ˜10 s with these methodologies.

  15. Efficient polymerization of acrylonitrile catalyzed by diValent lanthanide complex/sodium phenolate systems

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Four divalent lanthanide complexes Sm(ArO)2(THF)4, Yb(ArO)2(THF)3, Eu(ArO)2(THF)3 (ArO = 2,6-ditert-butyl-4-methylphenolate) and (ButCp)2Sm(THF)2 were synthesized. Their catalytic activities on the polymerization of acrylonitrile were studied. The catalytic activities were influenced by the central metal ions involved. The catalytic activities of these divalent lanthanide complexes can be greatly increased by adding NaOC~H2-2,6-But2-4-Me,NaOC6H4-4-But, or NaOC10H6-2-Me. The amount of additive has apparent effect on the catalytic activity, but the additive has no effect on the tacticity of the resulting polyacrylonitrile

  16. Innovative Application of Biopolymer Keratin as a Filler of Synthetic Acrylonitrile-Butadiene Rubber NBR

    Directory of Open Access Journals (Sweden)

    Mirosława Prochoń

    2013-01-01

    Full Text Available The current investigations show the influence of keratin, recovered from the tanning industry, on the thermal and mechanical properties of vulcanizates with synthetic rubber acrylonitrile-butadiene rubber NBR. The addition of waste protein to NBR vulcanizates influences the improvement of resistance at high temperatures and mechanical properties like tensile strength and hardness. The introduction of keratin to the mixes of rubber previously blended with zinc oxide (ZnO before vulcanization process leads to an increase in the cross-linking density of vulcanizates. The polymer materials received including addition of proteins will undergo biodecomposition in natural conditions. After soil test, vulcanizates with keratin especially keratin with ZnO showed much more changes on the surface area than vulcanizates without protein. In that aerobic environment, microorganisms, bacteria, and fungus digested better polymer materials containing natural additives.

  17. Barrierity of hydrogenated butadiene-acrylonitrile rubber and butyl rubber after exposure to organic solvents.

    Science.gov (United States)

    Krzemińska, Sylwia; Rzymski, Władysław M

    2011-01-01

    Resistance of antichemical clothing primarily depends on the type of material it is made from, in particular on the type of polymer used for coating the fabric carrier. This paper reports on systematic investigations on the influence of the cross-linking density of an elastomer and the composition of a cross-linked elastomer on its resistance to permeation of selected organic solvents. Tests of barrier material samples made from nonpolar butyl rubber (IIR) and polar hydrogenated butadiene-acrylonitrile rubber (HNBR) showed that (a) in rubber-solvent systems with medium thermodynamic affinity, cross-linking density influenced resistance to permeation and (b) the polarity of the system had a significant influence on barrierity.

  18. Improved procedure for determination of acrylonitrile in foods and its application to meat.

    Science.gov (United States)

    Page, B D; Charbonneau, C F

    1985-01-01

    The previously described headspace-gas chromatographic procedure for the determination of acrylonitrile (AN) in several foods, with N/P selective detection, has been modified to include packaged luncheon meats. The loss of AN during equilibration at 100 degrees C in meat samples as well as the previously described loss in cold pack cheese and peanut butter has been studied. The loss of AN could be prevented by the addition of 10% phosphoric acid, which increases the acidity of the food-acid-salt slurry to pH 1.2-1.5. This acidification permits detection of AN at 2 ppb (5% FSD at 16 X 10(-2) amp/mV) in all foods studied. AN was not detected in 10 samples of luncheon meat packaged in AN-based plastic which contained up to 2.6 ppm AN.

  19. Thermo-Physical Properties of Kenaf-Filled Acrylonitrile Butadiene Styrene Composites

    Directory of Open Access Journals (Sweden)

    Nikmatin Siti

    2017-01-01

    Full Text Available Studies on advantageous of natural fillers incorporated into polymer composites on thermo-physical and mechanical properties are still intensively investigated. Several evidences suggest that the natural fillers with small contents combined with polymer increase their composite properties. We thus investigate thermo-physical properties of kenaf-filled acrylonitrile butadiene styrene (ABS composites. ABS with 5% kenaf microparticle size (ABS/K5, ABS with 5% kenaf short fiber (ABS/KSF5, and recycled ABS with 5% kenaf microparticle size (RABS/K5 were manufactured. Granular composites were manufactured by the twin screw extruder. Composite properties in terms of X-ray diffractions, surface morphologies, and thermal behaviors were investigated. The present work found that ABS/KSF5 has the highest degree of crystallinity compared to others. No significant difference was found in terms of thermal properties of the composites.

  20. Comparison of cancer risks projected from animal bioassays to epidemiologic studies of acrylonitrile-exposed workers.

    Science.gov (United States)

    Ward, C E; Starr, T B

    1993-10-01

    Bioassay findings have demonstrated that acrylonitrile (ACN) is a rodent carcinogen, but the available epidemiologic evidence provides little support for the human carcinogenicity of ACN. This discordance between laboratory animal and human study findings is explored by determining post hoc the statistical power of 11 epidemiologic studies of ACN-exposed workers to detect the all-site and brain cancer excesses that are projected from rodent drinking water bioassay data. At reasonable estimates of the level and duration of exposures among the occupational cohorts, a majority of the human studies had sufficient power (> 80%) to detect the projected excesses, yet such responses were consistently absent. We conclude, subject to certain caveats, that the upper bound estimate of ACN's inhalation cancer potency of 1.5 x 10(-4) per ppm is too high to be consistent with the human ACN experience.

  1. Carcinogenicity and other health effects of acrylonitrile with reference to occupational exposure limit.

    Science.gov (United States)

    Sakurai, H

    2000-04-01

    The occupational exposure limit for acrylonitrile (AN) has been set by many organizations on the basis of its carcinogenicity. However, recent epidemiological studies do not afford evidence supporting the hypothesis that AN is carcinogenic to humans. Review of the 18 published cohort studies revealed that, although there is not adequate evidence in humans for carcinogenicity of AN, the possibility of a causal association between high exposure to AN and lung cancer in humans cannot be excluded. It was pointed out that carcinogenic potential of AN may be weak, if any, to humans, and the current occupational exposure limit (OEL) for AN of 2 ppm was evaluated as appropriate in view of AN exposure levels reported by epidemiological studies. Based also on review of the literature on health effects other than carcinogenicity, it was concluded that the current OEL for AN is a reasonable value and there is no need for a revision at present.

  2. Flame Retardant Effects of Nano-Clinoptilolite on AcrylonitrileButadiene-Styrene (ABS Nano-Composite

    Directory of Open Access Journals (Sweden)

    Aboulfazl Barati

    2012-01-01

    Full Text Available In recent years, intumescent technology has found a place in polymer science as a method of providing flame retardance to polymeric materials. On heating, fire-retardant intumescent material restricts the action of the heat flux or flame. The proposed mechanism is based on charred layer acting as physical barrier, which slows down heat and mass transfer between the gas and the condensed phases. In this paper, the flammability of intumescent fire-retardant acrylonitrile-butadiene-styrene (ABS matrix composites consisting of hydromagnesite (HMg as an acid source and blowing agent, pentaerythritol (PER as a carbonisation agent and natural zeolite (clinoptilolite rich, Kansar Shargh as a synergistic agent were examined. The flammability of composites was characterized by limiting oxygen index (LOI measurement and horizontal burning tests. A synergistic effect in flame retardancy was observed when natural zeolites were used in combination with HMg and PER.

  3. A flexible Li polymer primary cell with a novel gel electrolyte based on poly(acrylonitrile)

    Science.gov (United States)

    Akashi, Hiroyuki; Tanaka, Ko-ichi; Sekai, Koji

    The performance of a Li polymer primary cell with fire-retardant poly(acrylonitrile) (PAN)-based gel electrolytes is reported. By optimizing electrodes, electrolytes, the packaging material, and the structural design of the polymer cell, we succeeded in developing a "film-like" Li polymer primary cell with sufficient performance for practical use. The cell is flexible and less than 0.5 mm thick, which makes it suitable for a power source for some smart devices, such as an IC card. Fast cation conduction in the gel electrolyte minimizes the drop of the discharge capacity even at -20 °C. The high chemical stability of the gel electrolytes and the new packaging material allow the self-discharge rate to be limited to under 4.3%, which is equivalent to that of conventional coin-shaped or cylindrical Li-MnO 2 cells.

  4. Photoinitiated decomposition of substituted ethylenes: The photodissociation of vinyl chloride and acrylonitrile at 193 nm

    Energy Technology Data Exchange (ETDEWEB)

    Blank, D.A.; Suits, A.G.; Lee, Y.T. [Lawrence Berkeley National Lab., CA (United States)] [and others

    1997-04-01

    Ethylene and its substituted analogues (H{sub 2}CCHX) are important molecules in hydrogen combustion. As the simplest {pi}-bonded hydrocarbons these molecules serve as prototypical systems for understanding the decomposition of this important class of compounds. The authors have used the technique of photofragment translational spectroscopy at beamline 9.0.2.1 to investigate the dissociation of vinyl chloride (X=Cl) and acrylonitrile (X=CN) following absorption at 193 nm. The technique uses a molecular beam of the reactant seeded in helium which is crossed at 90 degrees with the output of an excimer laser operating on the ArF transition, 193.3 nm. The neutral photoproducts which recoil out of the molecular beam travel 15.1 cm where they are photoionized by the VUV undulator radiation, mass selected, and counted as a function of time. The molecular beam source is rotatable about the axis of the dissociation laser. The authors have directly observed all four of the following dissociation channels for both systems: (1) H{sub 2}CCHX {r_arrow} H + C{sub 2}H{sub 2}X; (2) H{sub 2}CCHX {r_arrow} X + C{sub 2}H{sub 3}; (3) H{sub 2}CCHX {r_arrow} H{sub 2} + C{sub 2}HX; and (4) H{sub 2}CCHX {r_arrow} HX + C{sub 2}H{sub 2}. They measured translational energy distributions for all of the observed channels and measured the photoionization onset for many of the photoproducts which provided information about their chemical identity and internal energy content. In the case of acrylonitrile, selective product photoionization provided the ability to discriminate between channels 2 and 4 which result in the same product mass combination.

  5. Perinatal Toxicity and Carcinogenicity Studies of Styrene –Acrylonitrile Trimer, A Ground Water Contaminant

    Science.gov (United States)

    Behl, Mamta; Elmore, Susan A.; Malarkey, David E.; Hejtmancik, Milton R.; Gerken, Diane K.; Chhabra, Rajendra S.

    2015-01-01

    Styrene Acrylonitrile (SAN) Trimer is a by-product in the production of acrylonitrile styrene plastics. Following a report of a childhood cancer cluster in the Toms River section of Dover Township, New Jersey, SAN Trimer was identified as one of the groundwater contaminants at Reich Farm Superfund site in the township. The contaminants from the Reich Farm site’s ground water plume impacted two wells at the Parkway well field. The National Toxicology Program (NTP) studied the toxicity and carcinogenicity of SAN Trimer in rats exposed during their perinatal developmental period and adulthood. The chronic toxicity and carcinogenicity studies in F344/N rats were preceded by 7- and 18-week perinatal toxicity studies to determine the exposure concentrations for the 2-year studies. Subsequently, Fisher 344 pregnant dams were exposed to SAN Trimer containing diet at 400, 800, or 1600 ppm concentrations during gestation, nursing and weaning periods of offspring followed by two year of adult exposures to both male and female pups. There was no statistically significant evidence of carcinogenic activity following SAN-Trimer exposure; however, rare neoplasms in the brain and spinal cord were observed in males and to lesser extent in female rats. These incidences were considered within the range of historical background in the animal model used in the current studies. Therefore, the presence of a few rarely occurring CNS tumors in the treated groups were not judged to be associated with the SAN Trimer exposure. The major finding was a dose-related peripheral neuropathy associated with the sciatic nerves in females and spinal nerve roots in males and females thereby suggesting that SAN trimer is potentially a nervous system toxicant. PMID:24060431

  6. Perinatal toxicity and carcinogenicity studies of styrene-acrylonitrile trimer, a ground water contaminant.

    Science.gov (United States)

    Behl, Mamta; Elmore, Susan A; Malarkey, David E; Hejtmancik, Milton R; Gerken, Diane K; Chhabra, Rajendra S

    2013-12-06

    Styrene acrylonitrile (SAN) trimer is a by-product in the production of acrylonitrile styrene plastics. Following a report of a childhood cancer cluster in the Toms River section of Dover Township, New Jersey, SAN Trimer was identified as one of the groundwater contaminants at Reich Farm Superfund site in the township. The contaminants from the Reich Farm site's ground water plume impacted two wells at the Parkway well field. The National Toxicology Program (NTP) studied the toxicity and carcinogenicity of SAN Trimer in rats exposed during their perinatal developmental period and adulthood. The chronic toxicity and carcinogenicity studies in F344/N rats were preceded by 7- and 18-week perinatal toxicity studies to determine the exposure concentrations for the 2-year studies. Subsequently, Fisher 344 pregnant dams were exposed to SAN Trimer containing diet at 400, 800, or 1600ppm concentrations during gestation, nursing and weaning periods of offspring followed by two year of adult exposures to both male and female pups. There was no statistically significant evidence of carcinogenic activity following SAN-Trimer exposure; however, rare neoplasms in the brain and spinal cord were observed in males and to lesser extent in female rats. These incidences were considered within the range of historical background in the animal model used in the current studies. Therefore, the presence of a few rarely occurring CNS tumors in the treated groups were not judged to be associated with the SAN Trimer exposure. The major finding was a dose-related peripheral neuropathy associated with the sciatic nerves in females and spinal nerve roots in males and females thereby suggesting that SAN Trimer is potentially a nervous system toxicant.

  7. Immunoassay of haemoglobin-acrylonitrile adduct in rat as a biomarker of exposure.

    Science.gov (United States)

    L Wong Yu Ting Zheng Junyu Li Carlo H Tamburro Frederick W Benz, J

    1998-01-01

    Acrylonitrile (AN) is a rat carcinogen. Human exposure may come from chemical industries and smoking. A haemoglobin adduct of acrylonitrile (Hb-AN) has been used as a biomarker of exposure by means of gas chromatography-mass spectrometry (GC-MS) analysis. We have developed specific monoclonal antibodies (Mab) to human Hb-AN and wish to report evaluation of an immunoassay in rats using an Mab that cross-reacts with rat Hb-AN. A dose response study of LD 0, 10, 50, and 90 in Sprague-Dawley rats was undertaken, with each rat receiving \\[2,3-14C]AN at 50 Ci kg-1 sc, and Hb from an aliquot of blood was taken for covalent binding analysis by liquid scintillation spectrometry and fluorescence ELISA. The dose responses of rats at 0.25, 0.5, 1.0, and 2.0 h after AN doses of 20, 50, 80, 115 mg kg-1 were compared by both methods with Hb and globin samples. Regression analysis showed a linear relationship between immunoassay and 14C-AN binding. This indicates that an antigenic form of Hb-AN may be used as a surrogate of Hb-AN adduct. The sensitivity of ELISA was tested in rats exposed for 1 h to sub-toxic doses of AN (10-1.1 mg kg-1). Quantification of Hb-AN by immunoassay was achieved by calibration with a synthetic adduct HbAN4h, a reference adduct prepared by treating rat Hb with excess AN for 4 h. ELISA and GC-MS analysis of N-terminal valine-AN in the Hb-AN adduct were compared and similar detection levels were found. This rat study appears to have validated the new immunoassay method for biomonitoring of AN exposure.

  8. 提高丙烯腈回收率的一种新型急冷工艺和急冷塔%A new quenching process and tower to improve the recovery of acrylonitrile

    Institute of Scientific and Technical Information of China (English)

    甘永胜; 顾军民; 方永成

    2004-01-01

    Quenching process and design of the quenching tower in acrylonitrile production in China were studied in order to decrease the polymerization loss of acrylonitrile in the quenching tower.Based on the research of acrylonitrile polymerization in the quenching tower,a new quenching process was proposed to avoid the disadvantages of the original process.Two kinds of internals were installed to improve the performance of the quenching tower.Through a series of air-flow and real-flow model experiments,the new quenching process and new design were showed to be successful in enhancing the mass and heat transfer in the vapor-liquid system and decreasing the loss of acrylonitrile.Industrial application showed satisfactory results of decrease of the acrylonitrile loss in the quenching tower by about 4.5% and increase of the acrylonitrile recovery of the whole plant by more than 4%.

  9. Synthesis and Thermal Properties of Acrylonitrile/Butyl Acrylate/Fumaronitrile and Acrylonitrile/Ethyl Hexyl Acrylate/Fumaronitrile Terpolymers as a Potential Precursor for Carbon Fiber

    Directory of Open Access Journals (Sweden)

    Siti Nurul Ain Md Jamil

    2014-09-01

    Full Text Available A synthesis of acrylonitrile (AN/butyl acrylate (BA/fumaronitrile (FN and AN/EHA (ethyl hexyl acrylate/FN terpolymers was carried out by redox polymerization using sodium bisulfite (SBS and potassium persulphate (KPS as initiator at 40 °C. The effect of comonomers, BA and EHA and termonomer, FN on the glass transition temperature (Tg and stabilization temperature was studied using Differential Scanning Calorimetry (DSC. The degradation behavior and char yield were obtained by Thermogravimetric Analysis. The conversions of AN, comonomers (BA and EHA and FN were 55%–71%, 85%–91% and 76%–79%, respectively. It was found that with the same comonomer feed (10%, the Tg of AN/EHA copolymer was lower at 63 °C compared to AN/BA copolymer (70 °C. AN/EHA/FN terpolymer also exhibited a lower Tg at 63 °C when compared to that of the AN/BA/FN terpolymer (67 °C. By incorporating BA and EHA into a PAN system, the char yield was reduced to ~38.0% compared to that of AN (~47.7%. It was found that FN reduced the initial cyclization temperature of AN/BA/FN and AN/EHA/FN terpolymers to 228 and 221 °C, respectively, in comparison to that of AN/BA and AN/EHA copolymers (~260 °C. In addition, FN reduced the heat liberation per unit time during the stabilization process that consequently reduced the emission of volatile group during this process. As a result, the char yields of AN/BA/FN and AN/EHA/FN terpolymers are higher at ~45.1% and ~43.9%, respectively, as compared to those of AN/BA copolymer (37.1% and AN/EHA copolymer (38.0%.

  10. REDUCING NONSELECTIVE PROTEIN ADSORPTION AND CELL ADHESION ON POLYACRYLONITRILE FILMS BY COPOLYMERIZATION OF ACRYLONITRILE WITH α-ALLYL GLUCOSIDE

    Institute of Scientific and Technical Information of China (English)

    Rui-qiang Kou; Chao Qu; Zhi-kang Xu; You-yi Xu; Ke Yao

    2003-01-01

    In this work, the surface properties of novel sugar-containing polymers, α-allyl glucoside (AG)/acrylonitrile (AN)copolymers, were studied by contact angle, protein adsorption and cell adhesion measurements. It was found that the contact angle of the copolymer films decreased from 68° to 30° with the increase of AG content in the copolymer. The adsorption amount of bovine serum albumin (BSA) and the adhesive macrophage onto the film surface also decreased significantly with increasing α-allyl glucoside content from 0 to 42 wt% in the copolymer. These preliminary results reveal that both the hydrophilicity and the biocompatibility of polyacrylonitrile-based membranes could be improved by copolymerizing acrylonitrile with vinyl carbohydrates.

  11. Genotoxicity of styrene-acrylonitrile trimer in brain, liver, and blood cells of weanling F344 rats.

    Science.gov (United States)

    Hobbs, Cheryl A; Chhabra, Rajendra S; Recio, Leslie; Streicker, Michael; Witt, Kristine L

    2012-04-01

    Styrene-acrylonitrile Trimer (SAN Trimer), a by-product in production of acrylonitrile styrene plastics, was identified at a Superfund site in Dover Township, NJ, where childhood cancer incidence rates were elevated for a period of several years. SAN Trimer was therefore tested by the National Toxicology Program in a 2-year perinatal carcinogenicity study in F344/N rats and a bacterial mutagenicity assay; both studies gave negative results. To further characterize its genotoxicity, SAN Trimer was subsequently evaluated in a combined micronucleus (MN)/Comet assay in juvenile male and female F344 rats. SAN Trimer (37.5, 75, 150, or 300 mg/kg/day) was administered by gavage once daily for 4 days. Micronucleated reticulocyte (MN-RET) frequencies in blood were determined by flow cytometry, and DNA damage in blood, liver, and brain cells was assessed using the Comet assay. Highly significant dose-related increases (P exposure to SAN Trimer.

  12. Genotoxicity of Styrene–Acrylonitrile Trimer in Brain, Liver, and Blood Cells of Weanling F344 Rats

    Science.gov (United States)

    Hobbs, Cheryl A.; Chhabra, Rajendra S.; Recio, Leslie; Streicker, Michael; Witt, Kristine L.

    2012-01-01

    Styrene–acrylonitrile Trimer (SAN Trimer), a by-product in production of acrylonitrile styrene plastics, was identified at a Superfund site in Dover Township, NJ, where childhood cancer incidence rates were elevated for a period of several years. SAN Trimer was therefore tested by the National Toxicology Program in a 2-year perinatal carcinogenicity study in F344/N rats and a bacterial mutagenicity assay; both studies gave negative results. To further characterize its genotoxicity, SAN Trimer was subsequently evaluated in a combined micronucleus (MN)/Comet assay in juvenile male and female F344 rats. SAN Trimer (37.5, 75, 150, or 300 mg/kg/day) was administered by gavage once daily for 4 days. Micronucleated reticulocyte (MN-RET) frequencies in blood were determined by flow cytometry, and DNA damage in blood, liver, and brain cells was assessed using the Comet assay. Highly significant dose-related increases (P exposure to SAN Trimer. PMID:22351108

  13. Improved Method for Preparation of Amidoxime Modified Poly(acrylonitrile-co-acrylic acid: Characterizations and Adsorption Case Study

    Directory of Open Access Journals (Sweden)

    Nur Amirah Mohd Zahri

    2015-07-01

    Full Text Available Redox polymerization of poly(acrylonitrile-co-acrylic acid (poly(AN-co-AA is performed at 40 °C under N2 gas by varying the ratio of acrylonitrile (AN and acrylic acid (AA in the feed. The yield production of poly(acrylonitrile (PAN is 73% and poly(AN-co-AA with a feed ratio of 93:7 is the highest yield (72%. The PAN and poly(AN-co-AA are further chemically modify with hydroxylamine hydrochloride. The FTIR spectroscopy is used to confirm the copolymerization of poly(AN-co-AA and chemical modification of poly(AN-co-AA. Elemental microanalysis shows that the overall trend percentage of carbon, hydrogen, and nitrogen for all feed ratios are slightly decreasing as the feed ratio of AA is increasing except for poly(AN-co-AA 93:7. The SEM images shows that spherical diameter of poly(AN-co-AA is smaller compared to the PAN and amidoxime (AO modified poly(AN-co-AA. The TGA (thermogravimetric analysis analysis reveals that the poly(AN-co-AA degrades at lower temperatures compared to the PAN but higher than AO modified poly(AN-co-AA. The case study adsorption test showed that the AO modified poly(AN-co-AA 93:7 had the highest percentage removal of Cd2+ and Pb2+.

  14. Experimental Investigations on Tribological Behaviour of Alumina Added Acrylonitrile Butadiene Styrene (ABS Composites

    Directory of Open Access Journals (Sweden)

    T. Panneerselvam

    2016-09-01

    Full Text Available Composite materials are multifunctional in nature, which can be custom-made based on the nature of the applications. The challenge of composite materials lie on complementing the properties of one another i.e. materials which go in the making of composites strengthen each other by inhibiting their weaknesses. Polymers are one of the widely used materials which serve a wide spectrum of engineering needs. In the present work, the tribological behaviour of a composite containing Acrylonitrile Butadiene Styrene (ABS and traces of Alumina is experimentally investigated. Alumina is added to ABS in various percentages such as 1%, and 3% by weight in order to improve the wear resistance of the polymer. Central Composite Design was used to design the experiments and a standard Pin-On-Disk apparatus was used to conduct the experiments. It is observed from the test results that the addition of alumina significantly enhances the wear behavior of the polymer. However, adding more percentage of alumina has led to adverse effect on wear resistance of polymer materials. Abrasive wear mechanism is found to be predominant in the case of alumina added composite materials. It is also found that 1% alumina added composite exhibits excellent wear properties compared to other materials.

  15. Barrier properties of hydrogenated acrylonitrile-butadiene rubber composites containing modified layered aluminosilicates

    Science.gov (United States)

    Krzemińska, S.; Rzymski, W. M.

    2011-12-01

    The resistance to permeation by the selected solvents of flat membranes made of cured hydrogenated acrylonitrile-butadiene rubber (HNBR) materials without any fillers and containing 5 phr of layered aluminosilicate nanofiller (bentonite), modified with various types of ammonium salts or N330 type carbon black, was investigated. The barrier properties were assessed on the basis of the breakthrough time of a liquid with low (cyclohexane) or average (butyl acetate) thermodynamic affinity to HNBR, determined according to EN 6529:2001, through a cured elastomer sample. The addition of bentonite, irrespectively of the method of modification of its particles, was found to increase the cured HNBR breakthrough time by 20 - 35 % in the case of slowly permeating non-polar cyclohexane, and by 50 - 130 % in the case of polar butyl acetate permeating more rapidly, in comparison with the barrier material containing no filler. The layered aluminosilicate nanofillers increased the breakthrough time of the material sample for both the tested solvents. In particular, the breakthrough time for polar butyl acetate was even longer than for conventional carbon black. Additionally, the increase of the breakthrough time was observed to depend on the modifier of bentonite particle surface.

  16. Design and testing of digitally manufactured paraffin Acrylonitrile-butadiene-styrene hybrid rocket motors

    Science.gov (United States)

    McCulley, Jonathan M.

    This research investigates the application of additive manufacturing techniques for fabricating hybrid rocket fuel grains composed of porous Acrylonitrile-butadiene-styrene impregnated with paraffin wax. The digitally manufactured ABS substrate provides mechanical support for the paraffin fuel material and serves as an additional fuel component. The embedded paraffin provides an enhanced fuel regression rate while having no detrimental effect on the thermodynamic burn properties of the fuel grain. Multiple fuel grains with various ABS-to-Paraffin mass ratios were fabricated and burned with nitrous oxide. Analytical predictions for end-to-end motor performance and fuel regression are compared against static test results. Baseline fuel grain regression calculations use an enthalpy balance energy analysis with the material and thermodynamic properties based on the mean paraffin/ABS mass fractions within the fuel grain. In support of these analytical comparisons, a novel method for propagating the fuel port burn surface was developed. In this modeling approach the fuel cross section grid is modeled as an image with white pixels representing the fuel and black pixels representing empty or burned grid cells.

  17. Covalent Immobilization of Lipase on Poly ( acrylonitrile-co-maleic acid) Ultrafiltration Hollow Fiber Membrane

    Institute of Scientific and Technical Information of China (English)

    YE Peng; XU Zhi-kang; WU Jian; DENG Hong-tao; SETA Patrick

    2005-01-01

    Lipase from Candida rugosa was covalently immobilized on the surface of an ultrafiltration hollow fiber membrane fabricated from poly (acrylonitrile-co-maleic acid) (PANCMA) in which the carboxyl groups were activated with 1-ethyl-3-(dimethylaminopropyl) carbodiimide hydrochloride (EDC) and dicyclohexyl carbodiimide (DCC)/N-hydroxyl succinimide(NHS), respectively. The properties of the immobilized lipase were assayed and compared with those of the free enzyme. The maximum activities were observed in a relatively broader pH value range at high temperatures for the immobilized lipase compared to the free one. It was also found that the thermal and pH stabilities of lipase were improved upon immobilization and at 50 ℃ the thermal inactivation rate constant values are 2.1×10-2 for the free lipase, 3.2×10-3 for the immobilized lipase on the EDC-activated PANCMA membrane and 3.5×10-3 for the immobilized lipase on the DCC/NHS-activated PANCMA membrane, respectively.

  18. THERMAL DECOMPOSITION AND FLAMMABILITY OF ACRYLONITRILE-BUTADIENE-STYRENE/MULTI-WALLED CARBON NANOTUBES COMPOSITES

    Institute of Scientific and Technical Information of China (English)

    Li-fang Tong; Hai-yun Ma; Zheng-ping Fang

    2008-01-01

    Thermal and flammability properties of acrylonitrile-butadiene-styrene copolymer (ABS) with the addition of multi-walled carbon nanotubes (MWNTs) were studied. ABS/MWNTs composites were prepared via melt blending with the MWNTs content varied from 0.2% to 4.0% by mass. Thermogravimetry results showed that the addition of MWNTs accelerated the degradation of ABS during the whole process under air atmosphere, and both onset and maximum degradation temperature were lower than those of pure ABS. The destabilization effect of MWNTs on the thermal stability of the composites became unobvious under nitrogen, and the addition of MWNTs could improve the maximum degradation temperature. The heat release rate and time of ignition (tign) for the composites reduced greatly with the addition of MWNTs especially when the concentration of nanotubes was higher than 1.0%. The accumulation of carbon nanotubes with a network structure was observed and the char layer became thicker with increasing nanotubes concentration. Results from Raman spectra showed a higher degree of graphitization for the residues of ABS/MWNTs composites.

  19. An investigation on chloroprene-compatibilized acrylonitrile butadiene rubber/high density polyethylene blends

    Directory of Open Access Journals (Sweden)

    Khalil Ahmed

    2015-11-01

    Full Text Available Blends of acrylonitrile butadiene rubber/high density polyethylene (NBR/HDPE compatibilized by Chloroprene rubber (CR were prepared. A fixed quantity of industrial waste such as marble waste (MW, 40 phr was also included. The effect of the blend ratio and CR on cure characteristics, mechanical and swelling properties of MW-filled NBR/HDPE blends was investigated. The results showed that the MW-filled NBR/HDPE blends revealed an increase in tensile strength, tear, modulus, hardness and cross-link density for increasing weight ratio of HDPE. The minimum torque (ML and maximum torque (MH of blends increased with increasing weight ratio of HDPE while scorch time (ts2 cure time (tc90, compression set and abrasion loss of blends decreased with increasing weight ratio of HDPE. The blends also showed a continuous reduction in elongation at break as well as swelling coefficient with increasing HDPE amount in blends. MW filled blends based on CR provided the most encouraging balance values of overall properties.

  20. Hg(II) adsorption using amidoximated porous acrylonitrile/itaconic copolymers prepared by suspended emulsion polymerization.

    Science.gov (United States)

    Ji, Chunnuan; Qu, Rongjun; Chen, Hou; Liu, Xiguang; Sun, Changmei; Ma, Caixia

    2016-01-01

    Initially, porous acrylonitrile/itaconic acid copolymers (AN/IA) were prepared by suspended emulsion polymerization. Successively, the cyano groups in AN/IA copolymers were converted to amidoxime (AO) groups by the reaction with hydroxylamine hydrochloride. The structures of the AN/IA and amidoximated AN/IA (AO AN/IA) were characterized by infrared spectroscopy, scanning electron microscopy, and porous structural analysis. The adsorption properties of AO AN/IA for Hg(II) were investigated. The results show that AO AN/IA has mesopores and macropores, and surface area of 11.71 m(2) g(-1). It was found that AO AN/IA has higher affinity for Hg(II), with the maximum adsorption capacity of 84.25 mg g(-1). The AO AN/IA also can effectively remove Hg(II) from different binary metal ion mixture systems. Furthermore, the adsorption kinetics and thermodynamics were studied in detail. The adsorption equilibrium can quickly be achieved in 4 h determined by an adsorption kinetics study. The adsorption process is found to belong to the second-order model, and can be described by the Freundlich model.

  1. Peroxydisulfate initiated synthesis of potato starch-graft-poly(acrylonitrile under microwave irradiation

    Directory of Open Access Journals (Sweden)

    2007-01-01

    Full Text Available Potato starch-graft-poly(acrylonitrile could be efficiently synthesized using small concentration of ammonium peroxydisulfate (0.0014M in aqueous medium under microwave irradiation. A representative microwave synthesized graft copolymer was characterized using Fourier Transform Infrared Spectroscopy, X-ray Diffraction, Scanning Electron Microscopy and Thermogravimetric Analysis. Under microwave conditions oxygen removal from the reaction vessel was not required and the graft copolymer was obtained in high yield using very small amount of ammonium peroxydisulfate, however using the same amount of ammonium peroxydisulfate (0.0014M on thermostatic water bath no grafting was observed up to 98°C (even in inert atmosphere. Raising the concentration of the initiator to 0.24 M resulted into 10% grafting at 50 °C but in inert atmosphere.The viscosity/shear stability of the grafted starch (aqueous solution and water/saline retention ability of the microwave synthesized graft copolymer were also studied and compared with that of the native potato starch.

  2. Effects of acrylonitrile on lymphocyte lipid rafts and RAS/RAF/MAPK/ERK signaling pathways.

    Science.gov (United States)

    Li, X J; Li, B; Huang, J S; Shi, J M; Wang, P; Fan, W; Zhou, Y L

    2014-09-26

    Acrylonitrile (ACN) is a widely used chemical in the production of plastics, resins, nitriles, acrylic fibers, and synthetic rubber. Previous epidemiological investigations and animal studies have confirmed that ACN affects the lymphocytes and spleen. However, the immune toxicity mechanism is unknown. Lipid rafts are cell membrane structures that are rich in cholesterol and involved in cell signal transduction. The B cell lymophoma-10 (Bcl10) protein is a joint protein that is important in lymphocyte development and signal pathways. This study was conducted to examine the in vitro effects of ACN. We separated lipid rafts, and analyzed Bcl10 protein and caveolin. Western blotting was used to detect mitogen-activated protein kinase (MAPK) and phosphorylated MAPK levels. The results indicated that with increasing ACN concentration, the total amount of Bcl10 remained stable, but was concentrated mainly in part 4 to part 11 in electrophoretic band district which is high density in gradient centrifugation. Caveolin-1 was evaluated as a lipid raft marker protein; caveolin-1 content and position were relatively unchanged. Western blotting showed that in a certain range, MAPK protein was secreted at a higher level. At some ACN exposure levels, MAPK protein secretion was significantly decreased compared to the control group (P lipid raft structures, causing Bcl10 protein and lipid raft separation and restraining Ras-Raf-MAPK-extracellular signal-regulated kinase signaling pathways.

  3. Regenerated thermosetting styrene-co-acrylonitrile sandwich composite panels reinforced by jute fibre: structures and properties

    Indian Academy of Sciences (India)

    Jinglong Li; Qin Peng; Anrong Zeng; Junlin Li; Xiaole Wu; Xiaofei Liu

    2016-02-01

    Jute fibres-reinforced sandwich regenerated composite panels were fabricated using industrial waste thermosetting styrene-co-acrylonitrile (SAN) foam scraps via compression moulding for the purpose of recycling waste SAN foam and obtaining high physical performance. The jute fibres were, respectively, treated by heat, sodium hydroxide (NaOH) solution (5.0 wt%), and N,N-dimethylacetamide (DMAc) in order to improve the mechanical properties of the composites. The structures and mechanical properties of the composites were studied. The SAN matrix got compact and some crystalline region formed in SAN matrix via compression moulding. The composite reinforced by DMAc-treated jute fibres performed optimum mechanical properties among the regenerated panels whose impact strength, flexural strength, and compressive strength were 19.9 kJ m−2, 41.7 MPa, and 61.0 MPa, respectively. Good interfacial bonding between DMAc-treated fibres and SAN matrix was verified by peel test and exhibited in SEM photographs. Besides, the water absorption of DMAc-treated fibres composite was lower than other SAN/jute fibre-reinforced sandwich composite panels.

  4. Study of the Effect of Grafted Antioxidant on the Acrylonitrile-Butadiene Copolymer Properties

    Directory of Open Access Journals (Sweden)

    Abdulaziz Ibrahim Al-Ghonamy

    2010-01-01

    Full Text Available The grafting of ADPEA onto natural rubber was executed with UV radiation. Benzoyl peroxide was used to initiate the free-radical grafting copolymerization. Natural rubber-graft-N-(4-aminodiphenylether acrylamide (NR-g-ADPEA was characterized with an IR technique. The paper aims interested to determine the crosslinking density by using the ultrasonic technique. The ultrasonic velocities of both longitudinal and shear waves were measured in thermoplastic discs of NBR vulcanizates as a function of aging time. Ultrasonic velocity measurements were taken at 2 MHz ultrasonic frequency using the pulse echo method. We studied the effect of aging on the mechanical properties, crosslinking density, and the swelling and extraction phenomena for acrylonitrile-butadiene copolymer (NBR vulcanizates, which contained the prepared NR-g-ADPEA and a commercial antioxidant, N-isopropyl-−-phenyl-p-phenylenediamine. The prepared antioxidant enhanced both the mechanical properties of the NBR vulcanizates and the permanence of the ingredients in these vulcanizates.

  5. Method for the separation of high impact polystyrene (HIPS) and acrylonitrile butadiene styrene (ABS) plastics

    Science.gov (United States)

    Jody, Bassam J.; Arman, Bayram; Karvelas, Dimitrios E.; Pomykala, Jr., Joseph A.; Daniels, Edward J.

    1997-01-01

    An improved method is provided for separating acrylonitrile butadiene styrene (ABS) and high impact polystyrene (HIPS) plastics from each other. The ABS and HIPS plastics are shredded to provide a selected particle size. The shredded particles of the ABS and HIPS plastics are applied to a solution having a solution density in a predefined range between 1.055 gm/cm.sup.3 and 1.07 gm/cm.sup.3, a predefined surface tension in a range between 22 dynes/cm to 40 dynes/cm and a pH in the range of 1.77 and 2.05. In accordance with a feature of the invention, the novel method is provided for separating ABS and HIPS, two solid thermoplastics which have similar densities by selectively modifying the effective density of the HIPS using a binary solution with the appropriate properties, such as pH, density and surface tension, such as a solution of acetic acid and water or a quaternary solution having the appropriate density, surface tension, and pH.

  6. Acrylonitrile Butadiene Styrene (ABS) plastic based low cost tissue equivalent phantom for verification dosimetry in IMRT.

    Science.gov (United States)

    Kumar, Rajesh; Sharma, S D; Deshpande, Sudesh; Ghadi, Yogesh; Shaiju, V S; Amols, H I; Mayya, Y S

    2009-12-17

    A novel IMRT phantom was designed and fabricated using Acrylonitrile Butadiene Styrene (ABS) plastic. Physical properties of ABS plastic related to radiation interaction and dosimetry were compared with commonly available phantom materials for dose measurements in radiotherapy. The ABS IMRT phantom has provisions to hold various types of detectors such as ion chambers, radiographic/radiochromic films, TLDs, MOSFETs, and gel dosimeters. The measurements related to pre-treatment dose verification in IMRT of carcinoma prostate were carried out using ABS and Scanditronics-Wellhoffer RW3 IMRT phantoms for five different cases. Point dose data were acquired using ionization chamber and TLD discs while Gafchromic EBT and radiographic EDR2 films were used for generating 2-D dose distributions. Treatment planning system (TPS) calculated and measured doses in ABS plastic and RW3 IMRT phantom were in agreement within +/-2%. The dose values at a point in a given patient acquired using ABS and RW3 phantoms were found comparable within 1%. Fluence maps and dose distributions of these patients generated by TPS and measured in ABS IMRT phantom were also found comparable both numerically and spatially. This study indicates that ABS plastic IMRT phantom is a tissue equivalent phantom and dosimetrically it is similar to solid/plastic water IMRT phantoms. Though this material is demonstrated for IMRT dose verification but it can be used as a tissue equivalent phantom material for other dosimetry purposes in radiotherapy.

  7. Induction of oxidative stress and oxidative damage in rat glial cells by acrylonitrile.

    Science.gov (United States)

    Kamendulis, L M; Jiang, J; Xu, Y; Klaunig, J E

    1999-08-01

    Chronic treatment of rats with acrylonitrile (ACN) resulted in a dose-related increase in glial cell tumors (astrocytomas). While the exact mechanism(s) for ACN-induced carcinogenicity remains unresolved, non-genotoxic and possibly tumor promotion modes of action appear to be involved in the induction of glial tumors. Recent studies have shown that ACN induced oxidative stress selectively in rat brain in a dose-responsive manner. The present study examined the ability of ACN to induce oxidative stress in a rat glial cell line, a target tissue, and in cultured rat hepatocytes, a non-target tissue of ACN carcinogenicity. Glial cells and hepatocytes were treated for 1, 4 and 24 h with sublethal concentrations of ACN. ACN induced an increase in oxidative DNA damage, as evidenced by increased production of 8-hydroxy-2'-deoxyguanosine (8-OH-dG) in glial cells but not in rat hepatocytes. Hydroxyl radical formation following ACN treatment was also selectively increased in glial cells. Following 1 and 4 h of ACN exposure, the levels of the non-enzymatic antioxidant glutathione, as well as the activities of the enzymatic antioxidants catalase and superoxide dismutase were significantly decreased in the rat glial cells. Lipid peroxidation and the activity of glutathione peroxidase were not affected by ACN treatment in rat glial cells. No changes in any of these biomarkers of oxidative stress were observed in hepatocytes treated with ACN. These data indicate that ACN selectively induced oxidative stress in rat glial cells.

  8. Weight-of-the-evidence review of acrylonitrile reproductive and developmental toxicity studies.

    Science.gov (United States)

    Neal, Barbara H; Collins, James J; Strother, Dale E; Lamb, James C

    2009-01-01

    Risk assessment of acrylonitrile (AN) toxicity to humans has focused on potential carcinogenicity and acute toxicity. Epidemiological studies from China reported reproductive and developmental effects in AN workers, including infertility, birth defects, and spontaneous abortions. A weight-of-the-evidence (WoE) evaluation of the AN database assessed study strength, characterized toxicity, and identified no-observed-adverse-effect levels (NOAELs). The epidemiological studies do not demonstrate causality and are not sufficiently robust to be used for risk assessment. Rodent developmental studies showed fetotoxicity and malformations at maternally toxic levels; there was no unique developmental susceptibility. NOAELs for oral and inhalation exposures were 10 mg/kg/day and 12 ppm (6 h/day), respectively. Drinking-water and inhalation reproductive toxicity studies showed no clear effects on reproductive performance or fertility. Maternally toxic concentrations caused decreased pup growth. The drinking-water reproductive NOAEL was 100 ppm (moderate confidence due to study limitations). The inhalation exposure reproductive and neonatal toxicity high confidence NOAEL was 45 ppm (first generation 90 ppm) (6 h/day). The inhalation reproductive toxicity study provides the most robust data for risk assessment. Based on the WoE evaluation, AN is not expected to be a developmental or reproductive toxicant in the absence of significant maternal toxicity.

  9. 2-Cyanoethylmercapturic acid (CEMA) in the urine as a possible indicator of exposure to acrylonitrile.

    Science.gov (United States)

    Jakubowski, M; Linhart, I; Pielas, G; Kopecký, J

    1987-12-01

    The aim of this study was to evaluate the efficiency of metabolism of acrylonitrile (ACN) to N-acetyl-S-(2-cyanoethyl)-L-cysteine (2-cyanoethylmercapturic acid (CEMA) in man, the kinetics of excretion of this metabolite, and the relation between the uptake of ACN and the excretion of CEMA in urine. Eleven experiments were performed on six male volunteers exposed for eight hours to ACN at concentrations of 5 or 10 mg/m3. The average respiratory retention of ACN was 52% and 21.8% of the retained ACN was excreted as CEMA in urine. Elimination approximated first order kinetics with half life of about eight hours. The best correlation between the uptake of ACN in the lungs and excretion of CEMA in urine was obtained when the concentration of CEMA in the urine fraction, collected between the sixth and eighth hours after the beginning of exposure, was adjusted to a specific gravity of 1.016 (y = 0.33x-13.3; r = 0.83). CEMA excretion, however, cannot be used as an individual index of exposure.

  10. High-Energy-Density Poly(styrene-co-acrylonitrile) Thin Films

    Science.gov (United States)

    Wen, Fei; Xu, Zhuo; Xia, Weimin; Ye, Hongjun; Wei, Xiaoyong; Zhang, Zhicheng

    2013-12-01

    The dielectric response of poly(styrene-co-acrylonitrile) (PSAN) thin films fabricated by a solution casting process was investigated in this work. Linear dielectric behavior was obtained in PSAN films under an electric field at frequencies from 100 Hz to 1 MHz and temperature of -50°C to 100°C. The polymer films exhibited an intermediate dielectric permittivity of 4 and low dielectric loss (tan δ) of 0.027. Under 400 MV/m, the energy density of the PSAN films was 6.8 J/cm3, which is three times higher than that of biaxially oriented polypropylene (BOPP) (about 1.6 J/cm3). However, their charge-discharge efficiency (about 90%) was rather close to that of BOPP. The calculated effective dielectric permittivity of the PSAN films under high electric field was as high as 9, which may be attributed to the improved displacement of the cyanide groups (-CN) polarized at high electric fields. These high-performance features make PSAN attractive for high-energy-density capacitor applications.

  11. Cobalt-Mediated Radical Polymerization of Vinyl Acetate and Acrylonitrile in Supercritical Carbon Dioxide.

    Science.gov (United States)

    Kermagoret, Anthony; Chau, Ngoc Do Quyen; Grignard, Bruno; Cordella, Daniela; Debuigne, Antoine; Jérôme, Christine; Detrembleur, Christophe

    2016-03-01

    Cobalt-mediated radical polymerization (CMRP) of vinyl acetate (VAc) is successfully achieved in supercritical carbon dioxide (scCO2). CMRP of VAc is conducted using an alkyl-cobalt(III) adduct that is soluble in scCO2. Kinetics studies coupled to visual observations of the polymerization medium highlight that the melt viscosity and PVAc molar mass (Mn) are key parameters that affect the CMRP in scCO2. It is noticed that CMRP is controlled for Mn up to 10 000 g mol(-1), but loss of control is progressively observed for higher molar masses when PVAc precipitates in the polymerization medium. Low molar mass PVAc macroinitiator, prepared by CMRP in scCO2, is then successfully used to initiate the acrylonitrile polymerization. PVAc-b-PAN block copolymer is collected as a free flowing powder at the end of the process although the dispersity of the copolymer increases with the reaction time. Although optimization is required to decrease the dispersity of the polymer formed, this CMRP process opens new perspectives for macromolecular engineering in scCO2 without the utilization of fluorinated comonomers or organic solvents.

  12. Nanostructured synthetic carbons obtained by pyrolysis of spherical acrylonitrile/divinylbenzene copolymers.

    Directory of Open Access Journals (Sweden)

    Danish J Malik

    Full Text Available Novel carbon materials have been prepared by the carbonization of acrylonitrile (AN/divinylbenzene (DVB suspension porous copolymers having nominal crosslinking degrees in the range of 30-70% and obtained in the presence of various amounts of porogens. The carbons were obtained by pre-oxidation of AN/DVB copolymers at 250-350°C in air followed by pyrolysis at 850°C in an N(2 atmosphere. Both processes were carried out in one furnace and the resulting material needed no further activation. Resulting materials were characterized by XPS and low temperature nitrogen adsorption/desorption. It was found that maximum pyrolysis yield was ca. 50% depending on the oxidation conditions but almost independent of the crosslinking degree of the polymers. Porous structure of the carbons was characterized for the presence of micropores and macropores, when obtained from highly crosslinked polymers or polymers oxidized at 350°C and meso- and macropores in all other cases. The latter pores are prevailing in the structure of carbons obtained from less porous AN/DVB resins. Specific surface area (BET of polymer derived carbons can vary between 440 m(2/g and 250 m(2/g depending on the amount of porogen used in the synthesis of the AN/DVB polymeric precursors.

  13. Analysis of acrylonitrile, 1,3-butadiene, and related compounds in acrylonitrile-butadiene-styrene copolymers for kitchen utensils and children's toys by headspace gas chromatography/mass spectrometry.

    Science.gov (United States)

    Ohno, Hiroyuki; Kawamura, Yoko

    2010-01-01

    A headspace gas chromatography/mass spectrometry method was developed for the simultaneous determination of the residual levels of acrylonitrile (AN), 1,3-butadiene (1,3-BD), and their related compounds containing propionitrile (PN) and 4-vinyl-1-cyclohexene (4-VC) in acrylonitrile-butadiene-styrene (ABS) copolymers for kitchen utensils and children's toys. A sample was cut into small pieces, then N,N-dimethylacetamide and an internal standard were added in a sealed headspace vial. The vial was incubated for 1 h at 90 degrees C and the headspace gas was analyzed by gas chromatography/mass spectrometry. The recovery rates of the analytes were 93.3-101.8% and the coefficients of variation were 0.3-6.5%. In ABS copolymers, the levels were 0.3-50.4 microg/g for AN, ND-4.5 microg/g for PN, 0.06-1.58 microg/g for 1,3-BD, and 1.1-295 microg/g for 4-VC. The highest level was found for 4-VC, which is a dimer of 1,3-BD, and the next highest was for AN, which is one of the monomers of the ABS copolymer. Furthermore, the method was also applied to acrylonitrile-styrene (AS) copolymers and polystyrenes (PS) for kitchen utensils, and nitrile-butadiene rubber (NBR) gloves. In AS copolymers, AN and PN were detected at 16.8-54.5 and 0.8-6.9 microg/g, respectively. On the other hand, the levels in PS and NBR samples were all low.

  14. Acrylonitrile quenching of trp phosphorescence in proteins: a probe of the internal flexibility of the globular fold.

    Science.gov (United States)

    Strambini, Giovanni B; Gonnelli, Margherita

    2010-08-04

    Quenching of Trp phosphorescence in proteins by diffusion of solutes of various molecular sizes unveils the frequency-amplitude of structural fluctuations. To cover the sizes gap between O(2) and acrylamide, we examined the potential of acrylonitrile to probe conformational flexibility of proteins. The distance dependence of the through-space acrylonitrile quenching rate was determined in a glass at 77 K, with the indole analog 2-(3-indoyl) ethyl phenyl ketone. Intensity and decay kinetics data were fitted to a rate, k(r) =k(0) exp[-(r -r(0))/r(e)], with an attenuation length r(e) = 0.03 nm and a contact rate k(0) = 3.6 x 10(10) s(-1). At ambient temperature, the bimolecular quenching rate constant (kq) was determined for a series of proteins, appositely selected to test the importance of factors such as the degree of Trp burial and structural rigidity. Relative to kq = 1.9 x 10(9) M(-1)s(-1) for free Trp in water, in proteins kq ranged from 6.5 x 10(6) M(-1)s(-1) for superficial sites to 1.3 x 10(2) M(-1)s(-1) for deep cores. The short-range nature of the interaction and the direct correlation between kq and structural flexibility attest that in the microsecond-second timescale of phosphorescence acrylonitrile readily penetrates even compact protein cores and exhibits significant sensitivity to variations in dynamical structure of the globular fold.

  15. Pre-irradiation induced emulsion co-graft polymerization of acrylonitrile and acrylic acid onto a polyethylene nonwoven fabric

    Science.gov (United States)

    Liu, Hanzhou; Yu, Ming; Ma, Hongjuan; Wang, Ziqiang; Li, Linfan; Li, Jingye

    2014-01-01

    A pre-irradiation induced emulsion co-graft polymerization method was used to introduce acrylonitrile and acrylic acid onto a PE nonwoven fabric. The use of acrylic acid is meant to improve the hydrophilicity of the modified fabric. The kinetics of co-graft polymerization were studied. The existence of polyacrylonitrile (PAN) and poly(acrylic acid) (PAAc) graft chains was proven by Fourier transform infrared spectroscopy (FTIR) analysis. The existence of the nitrile groups in the graft chains indicates that they are ready for further amidoximation and adsorption of heavy metal ions.

  16. TERMINATION AND TRANSFER OF THE CHAIN RADICALS IN THE POLYMERIZATION OF ACRYLONITRILE INITIATED BY VANADIUM(V)-THIOUREA REDOX SYSTEM

    Institute of Scientific and Technical Information of China (English)

    WU Jinyuan; YANG Chaoxiong; WU Yuxian

    1990-01-01

    The dependence of the molecular weights on the concentration of reactants in the polymerization of acrylonitrile initiated by vanadium (V)-thiourea red ox system has been investigated. It was found that the molecular weights of the polymer change nonlinearly with increasing concentrations of nitric acid and thiourea. Probably, the composition of the complexes exert a great influence on the chain initiation and termination. The reaction of "complextermination " gives rise to the decrease of the molecular weights markedly while the concentrations of thiourea and vanadium (V)in the range from one to three molar ratios.

  17. Mechanistic diversity of the van Leusen reaction applied to 6-ketomorphinans and synthetic potential of the resulting acrylonitrile substructures.

    Science.gov (United States)

    Schütz, Johannes; Windisch, Petra; Kristeva, Elka; Wurst, Klaus; Ongania, Karl-Hans; Horvath, Ulrike E I; Schottenberger, Herwig; Laus, Gerhard; Schmidhammer, Helmut

    2005-06-24

    Tosylmethyl isocyanide was used to convert 7,8-didehydro-6-ketomorphinans to 6,7-didehydromorphinan-6-carbonitriles with retainment of the 4,5-epoxy ring. However, ring opening occurred in the presence of NaH giving 5,6,7,8-tetradehydromorphinan-6-carbonitriles. Addition of nucleophiles such as Li diisopropylamide or Grignard reagents to the acrylonitrile substructure yielded ring-opened 5,6-didehydro products. Seven products were characterized by X-ray crystal structure analysis and revealed insight into the mechanistic diversity of the van Leusen reaction.

  18. SELECTIVE SEPARATION OF WATER—ETHANOL MIXTURE THROUGH COPOLYMERIC MEMBRANES.Ⅱ.ACRYLONITRILE AND MALEIC ANHYDRIDE COPOLYMERIC MEMBRANES

    Institute of Scientific and Technical Information of China (English)

    ZHangFuyao; ZhangYifeng; 等

    1993-01-01

    Acrylonitrile(AN) and maleic anhydride(MA) copolymer has been synthesized by radical polymerization using ammonium persulfate and sodium bisulfite as initiator.The pervaporation properties of the copolymeric membranes prepared have been investigated for the first time. The dependences of pervaporation characteristics on coplymer composition,feed concentration and operating temperature have been studied.In order to improve the separation properties of the copolymeric membranes,the membranes were hydrolyzed with 10 wt% soldium hydroxide or potassium hydroxide aqueous solution.The hydrolyzed membranes containing more than 0.069MA mol fraction showed higher tensile strength and separation properties than the original membranes.

  19. Uncertainty and variability in the exposure reconstruction of chemical incidents--the case of acrylonitrile.

    Science.gov (United States)

    Huizer, Daan; Ragas, Ad M J; Oldenkamp, Rik; van Rooij, Joost G M; Huijbregts, Mark A J

    2014-12-15

    The application of human physiologically based pharmacokinetic (PBPK) modeling combined with measured biomonitoring data, has a great potential to backtrack external exposure to chemicals during chemical incidents. So far, an important shortcoming of 'reversed dosimetry' is that uncertainty and variability in the model predictions are often neglected. The aim of this paper is to characterize the variation in predicted environmental air concentrations by means of reversed dosimetry as a result of uncertainty in chemical-specific input data and variability in physiological parameters. Human biomonitoring data (N-2-cyanoethylvaline in blood) from a chemical incident with acrylonitrile (ACN) combined with the BioNormtox PBPK model are used as a case to reconstruct the air concentration and uncertainty thereof at the time of the incident. The influence of uncertainty in chemical-specific properties and exposure duration, and interindividual variability in physiological parameters on the reconstructed air exposure concentrations were quantified via nested Monte Carlo simulation. The range in the reconstructed air concentrations of ACN during the incident was within a factor of 3. Uncertainty in the exact exposure duration directly after the chemical accident was found to have a dominant influence on the model outcomes. It was also shown that uncertainty can be further reduced by collecting human biomonitoring data as soon as possible after the incident. Finally, the collection of specific information about individual physiological parameters from the victims, such as body weight, may further reduce the variation by 5 to 20% in our case study. Future research should include the comparison of reversed dosimetry model outcomes with measured air and biological concentrations to further increase the confidence in the model approach and its implementation in practice.

  20. Screening-level risk assessment for styrene-acrylonitrile (SAN) trimer detected in soil and groundwater.

    Science.gov (United States)

    Kirman, C R; Gargas, M L; Collins, J J; Rowlands, J C

    2012-01-01

    A screening-level risk assessment was conducted for styrene-acrylonitrile (SAN) Trimer detected at the Reich Farm Superfund site in Toms River, NJ. Consistent with a screening-level approach, on-site and off-site exposure scenarios were evaluated using assumptions that are expected to overestimate actual exposures and hazards at the site. Environmental sampling data collected for soil and groundwater were used to estimate exposure point concentrations. Several exposure scenarios were evaluated to assess potential on-site and off-site exposures, using parameter values for exposures to soil (oral, inhalation of particulates, and dermal contact) and groundwater (oral, dermal contact) to reflect central tendency exposure (CTE) and reasonable maximum exposure (RME) conditions. Three reference dose (RfD) values were derived for SAN Trimer for short-term, subchronic, and chronic exposures, based upon its effects on the liver in exposed rats. Benchmark (BMD) methods were used to assess the relationship between exposure and response, and to characterize appropriate points of departure (POD) for each RfD. An uncertainty factor of 300 was applied to each POD to yield RfD values of 0.1, 0.04, and 0.03 mg/kg-d for short-term, subchronic, and chronic exposures, respectively. Because a chronic cancer bioassay for SAN Trimer in rats (NTP 2011a) does not provide evidence of carcinogenicity, a cancer risk assessment is not appropriate for this chemical. Potential health hazards to human health were assessed using a hazard index (HI) approach, which considers the ratio of exposure dose (i.e., average daily dose, mg/kg-d) to toxicity dose (RfD, mg/kg-d) for each scenario. All CTE and RME HI values are well below 1 (where the average daily dose is equivalent to the RfD), indicating that there is no concern for potential noncancer effects in exposed populations even under the conservative assumptions of this screening-level assessment.

  1. Fabrication of Acrylonitrile-Butadiene-Styrene Nanostructures with Anodic Alumina Oxide Templates, Characterization and Biofilm Development Test for Staphylococcus epidermidis.

    Directory of Open Access Journals (Sweden)

    Camille Desrousseaux

    Full Text Available Medical devices can be contaminated by microbial biofilm which causes nosocomial infections. One of the strategies for the prevention of such microbial adhesion is to modify the biomaterials by creating micro or nanofeatures on their surface. This study aimed (1 to nanostructure acrylonitrile-butadiene-styrene (ABS, a polymer composing connectors in perfusion devices, using Anodic Alumina Oxide templates, and to control the reproducibility of this process; (2 to characterize the physico-chemical properties of the nanostructured surfaces such as wettability using captive-bubble contact angle measurement technique; (3 to test the impact of nanostructures on Staphylococcus epidermidis biofilm development. Fabrication of Anodic Alumina Oxide molds was realized by double anodization in oxalic acid. This process was reproducible. The obtained molds present hexagonally arranged 50 nm diameter pores, with a 100 nm interpore distance and a length of 100 nm. Acrylonitrile-butadiene-styrene nanostructures were successfully prepared using a polymer solution and two melt wetting methods. For all methods, the nanopicots were obtained but inside each sample their length was different. One method was selected essentially for industrial purposes and for better reproducibility results. The flat ABS surface presents a slightly hydrophilic character, which remains roughly unchanged after nanostructuration, the increasing apparent wettability observed in that case being explained by roughness effects. Also, the nanostructuration of the polymer surface does not induce any significant effect on Staphylococcus epidermidis adhesion.

  2. Fire and Gas Barrier Properties of Poly(styrene-co-acrylonitrile Nanocomposites Using Polycaprolactone/Clay Nanohybrid Based-Masterbatch

    Directory of Open Access Journals (Sweden)

    S. Benali

    2008-01-01

    Full Text Available Exfoliated nanocomposites are prepared by dispersion of poly(ε-caprolactone (PCL grafted montmorillonite nanohybrids used as masterbatches in poly(styrene-co-acrylonitrile (SAN. The PCL-grafted clay nanohybrids with high inorganic content are synthesized by in situ intercalative ring-opening polymerization of ε-caprolactone between silicate layers organomodified by alkylammonium cations bearing two hydroxyl functions. The polymerization is initiated by tin alcoholate species derived from the exchange reaction of tin(II bis(2-ethylhexanoate with the hydroxyl groups borne by the ammonium cations that organomodified the clay. These highly filled PCL nanocomposites (25 wt% in inorganics are dispersed as masterbatches in commercial poly(styrene-co-acrylonitrile by melt blending. SAN-based nanocomposites containing 3 wt% of inorganics are accordingly prepared. The direct blend of SAN/organomodified clay is also prepared for sake of comparison. The clay dispersion is characterized by wide-angle X-ray diffraction (WAXD, atomic force microscopy (AFM, and solid state NMR spectroscopy measurements. The thermal properties are studied by thermogravimetric analysis. The flame retardancy and gas barrier resistance properties of nanocomposites are discussed both as a function of the clay dispersion and of the matrix/clay interaction.

  3. EFFECT OF AMPHIPHILIC POLY (STYRENE-B-ETHYLENE OXIDE) DIBLOCK COPOLYMER INTERCALATED LAYERED SILICATE AS FILLER ON ACRYLONITRILE-BUTADIENE-STYRENE RESIN

    Institute of Scientific and Technical Information of China (English)

    Guo Tianying; Zhang Jie; Hao Guangjie; Song Moudao; Zhang Banghua

    2003-01-01

    The diblock copolymers intercalated layered silicate was prepared via a melt dispersion technique. Then the effect of intercalated hybrid as filler on acrylonitrile- butadiene-styrene resin was characterized by X-ray diffraction, transmission electron microscopy, stress-strain measurements in elongation.

  4. A COMPARISON BETWEEN THE MORPHOLOGY OF SEMICRYSTALLINE POLYMER BLENDS OF POLY(EPSILON-CAPROLACTONE)/POLY(VINYL METHYL-ETHER) AND POLY(EPSILON-CAPROLACTONE)/(STYRENE-ACRYLONITRILE)

    NARCIS (Netherlands)

    OUDHUIS, AACM; THIEWES, HJ; VANHUTTEN, PF; TENBRINKE, G

    1994-01-01

    The morphology of polymer blends of poly(epsilon-caprolactone) (PCL) and poly(vinyl methyl ether) (PVME) is compared with that of PCL and a random copolymer of styrene and acrylonitrile (SAN). The main objective is to determine the influence of the glass transition temperature of the amorphous compo

  5. Accurate quantification of the mercapturic acids of acrylonitrile and its genotoxic metabolite cyanoethylene-epoxide in human urine by isotope-dilution LC-ESI/MS/MS.

    Science.gov (United States)

    Schettgen, T; Bertram, J; Kraus, T

    2012-08-30

    Acrylonitrile is a highly important industrial chemical with a high production volume worldwide, especially in the plastics industry. It is classified as a possible human carcinogen by the International Agency for Research on Cancer (IARC group 2B). During metabolism of acrylonitrile, the genotoxic metabolite cyanoethylene-epoxide is formed. The urinary mercapturic acids of acrylonitrile, namely N-acetyl-S-(2-cyanoethyl)-L-cysteine (CEMA) and cyanoethylene-epoxide, namely N-acetyl-S-(1-cyano-2-hydroxyethyl)-L-cysteine (CHEMA) are specific biomarkers for the determination of individual internal exposure to acrylonitrile and its highly reactive metabolite. We have developed and validated a sensitive method for the accurate determination of CEMA and CHEMA in human urine with a multidimensional LC/MS/MS-method using deuterium-labelled analogues for both analytes as internal standards. Analytes were stripped from urinary matrix by online extraction on a restricted access material, transferred to the analytical column and determined by tandem mass spectrometry. The limit of quantification (LOQ) for CEMA and CHEMA was 1 μg/L urine and allowed to quantify the background exposure of the (smoking) general population. Precision within and between series for CHEMA ranged from 2.6 to 8.0% at four concentrations ranging from 8.3 to 86 μg/L urine, mean accuracy was between 94 and 100%. For CEMA, precision within and between series ranged from 2.4 to 14.5% at four concentrations ranging from 15.1 to 196 μg/L urine, mean accuracy was between 91 and 104%. We applied the method to spot urine samples of 83 subjects of the general population with no known occupational exposure to acrylonitrile. Median levels (range) for CEMA and CHEMA in urine samples of non-smokers (n=47) were 1.9 μg/L (<1-16.4 μg/L) and<1 μg/L (<1-3 μg/L), while in urine samples of smokers (n=36), median levels were 184 μg/L (2-907 μg/L) and 29.3 μg/L (<1-147 μg/L), respectively. Smokers showed a

  6. Fittings of unplasticized polyvinyl chloride (PVC-U), chlorinated polyvinyl chloride (PVC-C) or acrylonitrile/butadiene/styrene (ABS) with plain sockets for pipes under pressure - Dimensions of sockets - Metric series

    CERN Document Server

    International Organization for Standardization. Geneva

    1985-01-01

    Fittings of unplasticized polyvinyl chloride (PVC-U), chlorinated polyvinyl chloride (PVC-C) or acrylonitrile/butadiene/styrene (ABS) with plain sockets for pipes under pressure - Dimensions of sockets - Metric series

  7. ON THE KINETICS AND MECHANISM OF THE COPOLYMERIZATION OF ACRYLONITRILE WITH STYRENE IN THE PRESENCE OF COPPER CHLORIDE

    Institute of Scientific and Technical Information of China (English)

    Hiroko Sato; Hiroshi Tsuji; Hitoshi Sasaki; Shinichi Ikemura; Yasuhito Gotoh; Junzo Ishikawa; Sei-ichi Nishimoto

    2003-01-01

    The copolymerization of styrene (St) and acrylonitrile (AN) complexed with CuCl2 monomer by a free radical mechanism was performed using benzoyl peroxide as an initiator at 65℃ under N2 atmosphere for 150 min. The rate of polymerization (Rp) was found to increase linearly with the concentration (in mol/L) of CuCl2, AN and St through scaling relations. The activation energy of the copolymerization process in the presence and absence of CuCl2 was found to be 46.5 kJ/mol and 102 kJ/mol, respectively. The viscosity average molecular weight of the copolymer and the kp2/kt ratio were determired to further assess the accelerating effect of CuCl2 on the copolymerization process. The copolymerization process in the presence of CuCl2 has a radical complex mechanism.

  8. STUDY ON THE GASEOUS PRODUCTS OF HIGH TEMPERATURE PYROLYSIS OF ACRYLONITRILE POLYMERS BY ON-LINE FTIR METHOD

    Institute of Scientific and Technical Information of China (English)

    ZHAO Genxiang; CHEN Bangjie

    1987-01-01

    The gaseous products of high temperature pyrolysis (300℃ to 960℃) of acrylonitrile polymers were measured continuously under nitrogen atnosphere by on-line Fourier Transform Infrared Spectroscopic method (FTIR). From the variations of characteristic peaks it was found that the nitrogen of macromolecules evolved were mainly in the form of hydrogen cyanide and ammonia. During the pyrolysis amorphous carbonaceous element was formed, and crosslinked to form network structure. Three kinds of samples were used for comparison. The experimental results show that the gaseous products of volatile small molecules were HCN, NH3, CH4, C2H6 and cyanide. CO and CO2 were also formed when copolymers of PAN were thermally pyrolyzed.

  9. Free radical induced grafting of acrylonitrile on pre-treated rice straw for enhancing its durability and flame retardancy.

    Science.gov (United States)

    Mukherjee, Aparna; Halder, Seema; Datta, Deepshikha; Anupam, Kumar; Hazra, Biren; Kanti Mandal, Mrinal; Halder, Gopinath

    2017-01-01

    The present investigation highlights the feasibility of a polymer grafting process to enhance the durability and flame retardancy of rice straw towards application as a low cost roofing material. The success of this grafting methodology was perceived to depend upon a bi-step pre-treatment process encompassing delignification and inorganic salts dispersion. Subsequently free radical polymer grafting of acrylonitrile onto rice straw was implemented by immersion mechanism initiated by oxalic acid-potassium permanganate initiator. The percentage of grafting, limiting oxygen index (LOI), biodegradability of the grafted rice straw and grafting yield percentage was estimated to be 57%, 27%, 0.02% and 136.67%, respectively. The weight loss of polymer grafted rice straw implied its less biodegradability over raw straw. Thus, the process of grafting contrived in the present analysis can be a promising and reliable technique for the efficient utilization of rice straw as an inexpensive roofing element through the augmentation of its durability and flame retardancy.

  10. Pressure induced graft-co-polymerization of acrylonitrile onto Saccharum cilliare fibre and evaluation of some properties of grafted fibre

    Indian Academy of Sciences (India)

    A S Singha; Anjali Shama; Vijay Kumar Thakur

    2008-02-01

    In the present work, graft co-polymerization of acrylonitrile (AN) onto Saccharum cilliare fibre has been carried out in the presence of potassium persulphate and ferrous ammonium sulphate (FAS–KPS) as redox initiator. The reactions were carried out under pressure in an autoclave. Various reaction parameters such as pressure, time, pH, concentrations of initiator and monomer were optimized to get maximum graft yield (35.59%). Grafted and ungrafted Saccharum cilliare fibres were then subjected to evaluation of some of their properties like swelling behaviour in different solvents, moisture absorbance under different humidity levels, water uptake and resistance towards chemicals such as hydrochloric acid and sodium hydroxide. The characterization of the graft copolymers were carried out by FTIR spectrophotometer, X-ray diffraction (XRD) and scanning electron microscopic (SEM) studies.

  11. Study on Exothermic Oxidation of Acrylonitrile-butadiene-styrene (ABS Resin Powder with Application to ABS Processing Safety

    Directory of Open Access Journals (Sweden)

    Jenq-Renn Chen

    2010-08-01

    Full Text Available Oxidative degradation of commercial grade ABS (Acrylonitrile-butadiene-styrene resin powders was studied by thermal analysis. The instabilities of ABS containing different polybutadiene (PB contents with respect to temperature were studied by Differential Scanning Calorimeter (DSC. Thermograms of isothermal test and dynamic scanning were performed. Three exothermic peaks were observed and related to auto-oxidation, degradation and oxidative decomposition, respectively. Onset temperature of the auto-oxidation was determined to be around 193 °C. However, threshold temperature of oxidation was found to be as low as 140 °C by DSC isothermal testing. Another scan of the powder after degeneration in air showed an onset temperature of 127 °C. Reactive hazards of ABS powders were verified to be the exothermic oxidation of unsaturated PB domains, not the SAN (poly(styrene-acrylonitrile matrix. Heat of oxidation was first determined to be 2,800 ± 40 J per gram of ABS or 4,720 ± 20 J per gram of PB. Thermal hazards of processing ABS powder are assessed by adiabatic temperature rise at process conditions. IR spectroscopy associated with heat of oxidation verified the oxidative mechanism, and these evidences excluded the heat source from the degradation of SAN. A specially prepared powder of ABS without adding anti-oxidant was analyzed by DSC for comparing the exothermic behaviors. Exothermic onset temperatures were determined to be 120 °C and 80 °C by dynamic scanning and isothermal test, respectively. The assessment successfully explained fires and explosions in an ABS powder dryer and an ABS extruder.

  12. Theoretical and experimental investigations of the 2-(4-chlorophenyl)-3-{[5-(2-cyano-2-phenylethenyl)]furan-2-yl}acrylonitrile molecule as a potential acceptor in organic solar cells

    Science.gov (United States)

    Kazici, Mehmet; Bozar, Sinem; Aydin Yuksel, Sureyya; Ongul, Fatih; Gokce, Halil; Gunes, Serap; Yorur Goreci, Cigdem

    2016-06-01

    A novel soluble asymmetric acrylonitrile derivative, 2-(4-Chlorophenyl)-3-{[5-(2-cyano-2-phenylethenyl)]furan-2-yl}acrylonitrile (CPCPFA, 3) was synthesized in three steps by Knoevenagel condensation. The structure of the CPCPFA was characterized using UV-vis, FTIR, 1H NMR, 13C NMR, and LC-MS. CPCPFA was evaluated as an electron acceptor in bulk heterojunction organic solar cells. Its optical and electronic properties as well as photovoltaic performance were investigated.

  13. 丙烯腈生殖毒理学研究概况%An Overview of the Study of Acrylonitrile on Reproductive Toxiocology

    Institute of Scientific and Technical Information of China (English)

    吴鑫; 金泰; 钟先玖

    2000-01-01

    @@ 丙烯腈(acrylonitrile,ACN)为有机合成工业中广泛应用的一种重要单体物质,可合成腈纶纤维,丁腈橡胶,ABS工程塑料及某些树脂.1994年全世界的ACN生产量超过30亿磅,1995年已达到100亿磅的生产能力[1].

  14. IMPORTANT DESIGN POINTS FOR WASTE WATER INCINERATOR OF ACRYLONITRILE PLANT [39]%丙烯腈装置废水焚烧炉设计要点

    Institute of Scientific and Technical Information of China (English)

    丁天才

    2012-01-01

    Waste water incinerator of acryloni- trile plant treats the wastewater from the acrylo- nitrile plant to reach the environmental emission requirements and reclaims the waste heat. So it is the key equipment for the acrylonitrile plant. Taking a waste water incinerator of an acrylonitrile plant as an example, this article introduces and analyzes the process plan selection, refractory lining design and the Nox control of the waste water incinerator of acrylonitrile plant.%丙烯腈装置废水焚烧炉是丙烯腈装置的关键设备,处理来自丙烯腈装置的废水,使之达到环保的排放要求,同时回收废热,以某丙烯腈项目废水焚烧炉为例,介绍和分析了丙烯腈废水焚烧炉的工艺方案选择、耐火材料选择和NOx控制.

  15. Melt-processable hydrophobic acrylonitrile-based copolymer systems with adjustable elastic properties designed for biomedical applications.

    Science.gov (United States)

    Cui, J; Trescher, K; Kratz, K; Jung, F; Hiebl, B; Lendlein, A

    2010-01-01

    Acrylonitrile-based polymer systems (PAN) are comprehensively explored as versatile biomaterials having various potential biomedical applications, such as membranes for extra corporal devices or matrixes for guided skin reconstruction. The surface properties (e.g. hydrophilicity or charges) of such materials can be tailored over a wide range by variation of molecular parameters such as different co-monomers or their sequence structure. Some of these materials show interesting biofunctionalities such as capability for selective cell cultivation. So far, the majority of AN-based copolymers, which were investigated in physiological environments, were processed from the solution (e.g. membranes), as these materials are thermo-sensitive and might degrade when heated. In this work we aimed at the synthesis of hydrophobic, melt-processable AN-based copolymers with adjustable elastic properties for preparation of model scaffolds with controlled pore geometry and size. For this purpose a series of copolymers from acrylonitrile and n-butyl acrylate (nBA) was synthesized via free radical copolymerisation technique. The content of nBA in the copolymer varied from 45 wt% to 70 wt%, which was confirmed by 1H-NMR spectroscopy. The glass transition temperatures (Tg) of the P(AN-co-nBA) copolymers determined by differential scanning calorimetry (DSC) decreased from 58 degrees C to 20 degrees C with increasing nBA-content, which was in excellent agreement with the prediction of the Gordon-Taylor equation based on the Tgs of the homopolymers. The Young's modulus obtained in tensile tests was found to decrease significantly with rising nBA-content from 1062 MPa to 1.2 MPa. All copolymers could be successfully processed from the melt with processing temperatures ranging from 50 degrees C to 170 degrees C, whereby thermally induced decomposition was only observed at temperatures higher than 320 degrees C in thermal gravimetric analysis (TGA). Finally, the melt processed P

  16. Determination of Bound Acrylonitrile Content in Acrylonitrile-butadiene Rubber(NBR) by Infrared Spectroscopy Method%红外光谱法测定丁腈橡胶中的结合丙烯腈含量

    Institute of Scientific and Technical Information of China (English)

    高杜娟; 黄世英; 赵家琳; 刘俊保

    2015-01-01

    Infrared spectrometry in this article was used to determinate the bound acrylonitrile content in nitrile rubber( NBR). In the process of experimenting,the sample preparation conditions were determined and the stand-ard values of seven substitute standard sample were confirmed by Kjeldahl method,through which the quantitative calculation formula was get. And finally,the results were compared with the method of element analysis.%本文采用红外光谱法测定丁腈橡胶( NBR)中的结合丙烯腈含量,确定了样品前处理条件,通过凯氏定氮法确定7个代用标准胶中结合丙烯腈含量的标准值,得出了结合丙烯腈含量的定量计算公式,测试结果与元素分析法进行了对比。

  17. TEMPERATURE AND pH RESPONSE, AND SWELLING BEHAVIOR OF POROUS ACRYLONITRILE-ACRYLIC ACID COPOLYMER HYDROGELS

    Institute of Scientific and Technical Information of China (English)

    Jian Huang; Zhi-ming Huang; Yong-zhong Bao; Zhi-xue Weng

    2006-01-01

    Macroporous acrylonitrile-acrylic acid (AN-AA) copolymer hydrogels were synthesized by free-radical solution polymerizations, using ammonium persulfate (APS)/N,N,N',N'-tetramethylethylenediamine (TEMED) redox initiator system and alcohols porogens. The morphology, temperature and pH sensitive swelling behavior, and swelling kinetics of the resulting hydrogels were investigated. It was found that alcohol type and concentration had great influences on the pore structure and porosity of hydrogels. The pore size of hydrogel increases with the moderate increase of the length of alcohol alkyl chain. However, a further increase of alkyl length would result in the formation of cauliflower-like structure and the decrease of pore size. The porosity of hydrogels increases with the increase of porogen concentration in the polymerization medium. The hydrogels with macroporous structure swell or shrink much faster in response to the change of pH in comparison with the conventional hydrogel without macroporous structure. Furthermore, the response rate is closely related to the porosity of the hydrogels, which could be easily controlled by modulating the concentration of the porogen in the medium. The circular swelling behavior of hydrogels indicated the formation of a relaxing three-dimensional network.

  18. Free radical induced grafting of acrylonitrile on pre-treated rice straw for enhancing its durability and flame retardancy

    Directory of Open Access Journals (Sweden)

    Aparna Mukherjee

    2017-01-01

    Full Text Available The present investigation highlights the feasibility of a polymer grafting process to enhance the durability and flame retardancy of rice straw towards application as a low cost roofing material. The success of this grafting methodology was perceived to depend upon a bi-step pre-treatment process encompassing delignification and inorganic salts dispersion. Subsequently free radical polymer grafting of acrylonitrile onto rice straw was implemented by immersion mechanism initiated by oxalic acid-potassium permanganate initiator. The percentage of grafting, limiting oxygen index (LOI, biodegradability of the grafted rice straw and grafting yield percentage was estimated to be 57%, 27%, 0.02% and 136.67%, respectively. The weight loss of polymer grafted rice straw implied its less biodegradability over raw straw. Thus, the process of grafting contrived in the present analysis can be a promising and reliable technique for the efficient utilization of rice straw as an inexpensive roofing element through the augmentation of its durability and flame retardancy.

  19. STUDY ON THE POLYMERIZATION OF ACRYLONITRILE INITIATED BY POLYPROPYLENE-BASED VANADYL POLYIMIDODIACETATE——THIOUREA REDOX SYSTEM

    Institute of Scientific and Technical Information of China (English)

    Yang Chaoxiong; Wu Jinyun; Liang Zhenming; Feng Zhouquan

    1989-01-01

    The present paper deals with the kinetics of polymerization of acrylonitrile ( AN ) initiated by the redox system of polypropylene-based vanadyl polyimidodiacetate (PV)-thiourea (TU)in aqueous sulfuric acid in the temperature range from 25 to 40 ℃ . The polymerization rate was measured by varying the concentrations of monomer, vanadyl polyimidodiacetate, thiourea and sulfuric acid. The overall rate of polymerization was summarized as RP =2.2 × 105e-6.860/RT[AN]1.0[PV]0.50[ TU]1.5[H2SO4]2.0 The molecular weight of polyacrylonitrile based on the experimental data was:(-M)n=k·1/T·[AN]/[PV]0.50[TU]1.5[H2SO4]2.0 These results indicated that the chain radicals are terminated by combination and/or disproportionation rather than chain transfer. The cooperation effect of carboxylic groups and the macromolecular field effect of polymer supporter are the characters of vanadyl polyimidodiacetate such as the case reported in early paper[ 1 ].

  20. Correlation Between Miscibility and Rheological Characteristics of the Polystyrene (PS) and Poly(styrene-co-acrylonitrile) (PSAN) Blends

    Science.gov (United States)

    Marwat, Zafrullah Khan; Baloch, Musa Kaleem

    2016-11-01

    Rheological measurement has been an effective technique to characterize the miscibility of polymer blends. This article investigates the viscoelastic behavior of poly(styrene) (PS) and poly(styrene-co-acrylonitrile) (PSAN) binary solutions in tetrahydrofuran (THF) relative to PS/PSAN/THF ternary solutions mainly reporting the findings of the authors involving the correlation between the miscibility and rheological behavior. Rheological properties, such as shear viscosity, and shear stress as a function of shear rate were investigated for different blend compositions. Moreover, complex viscosity, loss and storage moduli were also investigated as functions of both the frequency and blend composition. The criterion of miscibility based on the rule of mixture has been discussed. The present study revealed very small window of miscibility as only composition, 50/50 showed values close to the additivity rule or intermediate to those of the neat polymers, thereby indicating very weak interactions between the blend components. On the basis of various findings during the rheological investigation, the blend under study is classified almost immiscible. Moreover, the obtained results also suggested that the miscibility depends on the blend composition and frequency.

  1. Carboxyl-terminated butadiene-acrylonitrile-toughened epoxy/carboxyl-modified carbon nanotube nanocomposites: Thermal and mechanical properties

    Directory of Open Access Journals (Sweden)

    H. F. Xie

    2012-09-01

    Full Text Available Carboxyl-modified multi-walled carbon nanotubes (MWCNT–COOHs as nanofillers were incorporated into diglycidyl ether of bisphenol A (DGEBA toughened with carboxyl-terminated butadiene-acrylonitrile (CTBN. The carboxyl functional carbon nanotubes were characterized by Fourier-transform infrared spectroscopy and thermogravimetric analysis. Furthermore, cure kinetics, glass transition temperature (Tg, mechanical properties, thermal stability and morphology of DGEBA/CTBN/MWCNT–COOHs nanocomposites were investigated by differential scanning calorimetry (DSC, dynamic mechanical analysis (DMA, universal test machine, thermogravimetric analysis and scanning electron microscopy (SEM. DSC kinetic studies showed that the addition of MWCNT–COOHs accelerated the curing reaction of the rubber-toughened epoxy resin. DMA results revealed that Tg of rubber-toughened epoxy nanocomposites lowered with MWCNT–COOH contents. The tensile strength, elongation at break, flexural strength and flexural modulus of DGEBA/CTBN/MWCNT-COOHs nanocomposites were increased at lower MWCNT-COOH concentration. A homogenous dispersion of nanocomposites at lower MWCNT–COOH concentration was observed by SEM.

  2. Molecular mechanism of gelation upon the addition of water to a solution of poly(acrylonitrile) in dimethylsulfoxide

    Science.gov (United States)

    Vettegren, V. I.; Kulik, V. B.; Savitskii, A. V.; Fetisov, O. I.; Usov, V. V.

    2010-05-01

    The solidification of a solution of poly(acrylonitrile) (PAN) in dimethylsulfoxide (DMSO) upon introduction of water into the solution is studied by Raman spectroscopy. In the absence of water, DMSO molecules are found to produce dipole-dipole bonds with PAN molecules. Upon the introduction of water, DMSO molecules produce hydrogen bonds with it and bands at 1005 and 1015 cm-1 appear in the Raman spectrum, which are assigned to the valence vibrations of S=O bonds involved in the hydrogen bonds. Simultaneously, water molecules produce hydrogen bonds with PAN molecules: R-C≡N...H-O-H...N≡C-R, where R is the carbon skeleton of a PAN molecule. Accordingly, a band at 2250 cm-1 arises in the Raman spectrum, which is assigned to the valence vibrations of C≡N bonds producing hydrogen bonds with a water molecule. When the water content is low and the DMSO concentration is high, the length of the hydrogen bonds varies in wide limits and the band at 2250 cm-1 is wide. As the water content rises, DMSO molecules come out of PAN, the variation of the hydrogen bond length in it decreases (the band at 2250 cm-1 narrows), and a high-viscosity system (gel) arises that consists of PAN molecules bonded to water molecules via “equally strong” hydrogen bonds.

  3. Reclamation of post-consumer plastics for development of polycarbonate and acrylonitrile butadiene styrene based nanocomposites with nanoclay

    Science.gov (United States)

    Zicans, Janis; Meri, Remo Merijs; Ivanova, Tatjana; Berzina, Rita; Saldabola, Ruuta; Maksimov, Robert

    2016-05-01

    Suitability of recycled acrylonitrile-butadiene-styrene (R-ABS) and recycled polycarbonate (R-PC) for the development of polymer matrix nanocomposites with organically modified nanoclay (OMMT) is evaluated in comparison to virgin polymers (V-ABS and V-PC) based systems. The influence of OMMT content on the structure as well as calorimetric, mechanical and thermal properties of virgin and recycled polymers containing systems is revealed. Increase in stiffness and strength of virgin and recycled polymers based systems is observed along with rising nanoclay content. However, it is observed that reinforcing efficiency of clays on the R-ABS containing systems is reduced to certain extent in comparison to those, based on virgin polymers. It is shown, that in the presence of OMMT approximation of glass transition temperatures of both polymeric components is observed, which can testify about certain improvement of compatibility between PC and ABS. Increment of the modulus of elasticity and yield strength of the nanocomposites is associated with anisodiametric shape of OMMT, as well as with intercalation of polymer within the interlaminar space of the clay nanoparticles. It is also demonstrated that addition of nanoclay improves thermogravimetric behavior of the investigated compositions. Consequently, it is suggested that nanoclays can be used as promising functional additives and replace halogenated flame-retardants, without reducing mechanical properties of the composites.

  4. Effect of PAHM (Poly-acrylonitrile Hollow Microsphere) addition on the Lightweight and Firing Behavior of Whiteware

    Science.gov (United States)

    Choi, H. S.; Pee, J. H.; Kim, G. H.; Kim, J. Y.; Cho, W. S.; Kim, K. J.

    2011-10-01

    The pore generation technology using PAHM (Poly-acrylonitrile Hollow Microsphere) was studied in order to reduce the weights of tableware. In this study, we verify the property of modified slurry and plasticity of green body by adding PAHM. The modified slurry was prepared by adding 25~55vol% of PAHM to the slurry for whiteware. The viscosity of slurry was controlled to be low value (25~45vol%). However, the viscosity of modified slurry increased and the plasticity of modified green body decreased inside the 45~55vol% range. The formed specimen by slip casting was fired at 1225 °C, 1240°C. As the amount of PAHM content increased, the weight decreased and the addition of 45vol/% of PAHM resulted in a weight drop of 39%. However, when the PAHM content increased, the strength decreases over 50%. This is caused by the presence of a large volume of surface defects (pores) and defects from the agglomeration of PAHM.

  5. N-acetyl-S-(1-cyano-2-hydroxyethyl)-L-cysteine, a new urinary metabolite of acrylonitrile and oxiranecarbonitrile.

    Science.gov (United States)

    Linhart, I; Smejkal, J; Novák, J

    1988-01-01

    Two mercapturic acids, i.e., N-acetyl-S-(1-cyano-2-hydroxyethyl)-L-cysteine (CHEMA) and N-acetyl-S-(2-hydroxyethyl)-L-cysteine (HEMA), were isolated from the urine of rats dosed with four successive doses of oxiranecarbonitrile (glycidonitrile, GN), 5 mg/kg, a reactive metabolic intermediate of acrylonitrile (AN). GC-MS analysis of methylated urine extracts from both AN- and GN-dosed rats showed another mercapturate which was identified as N-acetyl-S-(1-cyanoethenyl)-L-cysteine (1-CEMA) methyl ester using an authentic reference sample. The mass spectrum of this compound was very similar to that of a methylated metabolite of AN tentatively identified by Langvardt et al. (1980) as N-acetyl-3-carboxy-5-cyanothiazane (ACCT). In contrast, no ACCT was found in rats dosed with either GN or AN. Hence, there is no evidence for the formation of ACCT or its isomers in rats dosed with AN or GN. The methyl ester of 1-CEMA is formed artificially by dehydration of CHEMA methyl ester in the injector of the gas chromatograph.

  6. Identification of alkylbenzene sulfonate surfactants leaching from an acrylonitrile butadiene rubber as novel inhibitors of calcineurin activity.

    Science.gov (United States)

    Ito, Noboru; Shibuguchi, Nao; Ishikawa, Ryoki; Tanaka, Susumu; Tokita, Yoshiharu; Nakajima-Shimada, Junko; Hosaka, Kohei

    2013-01-01

    Calcineurin (CN) is a Ca(2+)/calmodulin (CaM) dependent serine/threonine protein phosphatase and plays important role in several cellular functions in both higher and lower eukaryotes. Here we report inhibition of CN by linear alkylbenzene sulfonate. The clue to the finding was obtained while identifying the inhibitory material leaching from acrylonitrile butadiene rubber used for packing. Using standard dodecylbenzene sulfonate (C12-LAS), we obtained strong inhibition of CN with a half maximal inhibitory concentration of 9.3 µM, whereas analogs such as p-octylbenzene sulfonate and SDS hardly or only slightly affected CN activity. Three alkaline phosphatases, derived from shrimp, bacteria, and calf-intestine, which exhibit similar enzymatic activities to CN, were not inhibited by C12-LAS at concentrations of up to 100 µM. Furthermore, C12-LAS did not inhibit Ca(2+)/CaM-dependent myosin light chain kinase activity when tested at concentrations of up to 36 µM. The results indicate that C12-LAS is a potent selective inhibitor of CN activity.

  7. Properties of hydrogenated butadiene-acrylonitrile rubber plasticized by hydroxyl terminated poly (butadiene-co-acrylonitrile)%端羟基液体丁腈橡胶增塑氢化丁腈橡胶的性能

    Institute of Scientific and Technical Information of China (English)

    李再峰; 董慧民; 刘晓丹; 李敏婷; 张成龙; 熊召举

    2011-01-01

    The hydrogenated butadiene-acrylonitrile( HNBR ) was plasticized by hydroxyl terminated poly ( butadiene-co-acrylonitrile ) ( HTBN ), the structure and properties of plasticized rubber were characterized with pulsed nuclear magnetic resonance, differential scanning calorimetry, thermogravimetric analysis and stress-strain test, and the plasticization effect of HTBN was compared with plasticizer TP-95,TP-90 B and TP-759. The results indicated that HTBN worked as the common plasticizer like TP-95, TP-90 B and TP-759, resulting in the decrease of HNBR Mooney viscosity, on the other hand, it worked as a reactive species, the free radical in the vulcanization system intiated the adjacent crosslinking reaction between HTBN double bond and HNBR macromolecular backbone , thus increasing the crosslinking density, tensile strength,modulus at 100% and Shore A hardness of vulcanizates, improving the heat resistance but the glass transition temperature ( no significant change ) .When HTBN was 3 phr, the tensile strength of HNBR vulcanizate reached 41. 7 MPa, the Mooney viscosity was lower and the heat aging property was better.%利用核磁共振仪、差示扫描量热仪、热重分析仪和材料拉伸试验机等研究了端羟基液体丁腈橡胶增塑氢化丁腈橡胶的结构与性能,并与增塑剂TP-95、TP-90 B及TP-759的增塑效果进行了对比.结果表明,端羟基液体丁腈橡胶增塑氢化丁腈橡胶后,一方面起到了与TP-95、TP-90 B和TP-759类似的增塑作用,如降低了混炼胶的门尼黏度;另一方面作为一种反应性增塑剂,在体系中自由基的引发下其结构双键与氢化丁腈橡胶分子主链发生了邻接交联反应,使硫化胶的交联密度、拉伸强度、100%定伸应力和硬度都增大,耐热性能提高,而玻璃化转变温度没有变化.端羟基液体丁腈橡胶用量为3份(质量)时其所增塑氢化丁腈橡胶的拉伸强度高达41.7 MPa,且具有较低的门尼黏度和较好的热老化性能.

  8. 丁腈橡胶臭氧化制备羧基丁腈橡胶%Preparation of carboxylated acrylonitrile-butadiene rubber by ozonization of acrylonitrile-butadiene rubber

    Institute of Scientific and Technical Information of China (English)

    刘健; 程斌

    2011-01-01

    Carboxylated acrylnitrile-butadiene rubber(CNBR) was prepared via ozonization of acrylonitrile-butadiene rubber(NBR) in butyl acetate.Effects of reaction time, reaction temperature, the ozone flow rate and NBR concentration on intrinsic viscosity and acid value of CNBR were investigated.The results showed that higher reaction temperature,higher ozone flow rate and lower concentration of NBR could obviously increase the content of carboxylic group in CNBR and shorten the chain length of NBR. However, the factor of reaction time had a different performance. At the beginning, the intrinsic viscosity of CNBR rapidly dropped, but kept unchanged from some moment. And there was no influence of reaction time on acid value of CNBR.%以臭氧氧化丁腈橡胶合成了羧基丁腈橡胶,研究了反应时间、反应温度、臭氧通入量及丁腈橡胶胶液质量浓度对产物特性黏数和酸值的影响.结果表明,以丁腈橡胶臭氧化制备羧基丁腈橡胶,在实验范围内,反应温度升高、增大臭氧通入量和降低丁腈橡胶胶液质量浓度可以提高羧基丁腈橡胶的羧基含量,降低丁腈橡胶的相对分子质量.但是反应时间的影响较为复杂,开始时丁腈橡胶相对分子质量降低很快,到达某个时刻后保持不变.反应时间对羧基丁腈橡胶的酸值没有影响.

  9. Preparation of acrylonitrile butadiene rubber by soap-free emulsion polymerization%无皂乳液聚合制备丁二烯-丙烯腈橡胶

    Institute of Scientific and Technical Information of China (English)

    桂强; 梁琨; 钟启林; 马朋高; 张元寿; 王真琴

    2011-01-01

    In this paper,soap-free acrylonitrile butadiene rubber was prepared using sulfate polymerisable emulsifier KD SE-10 by emulsion copolymerization at low temperature. The article studied the influence of the amount of polymerisable emulsifier on mooney viscosity, bound acrylonitrile content, the gel ratio, tensile strength and molecular weight. And the amount of KD SE-10 was determined as 2. 7%~3.0wt%. Acrylonitrile butadiene rubber prepared has the remarkable characteristics of high-strength,excellent oil resistance and narrow molecular weight distribution.%采用硫酸盐类可聚合乳化剂烯丙氧基壬基苯氧基丙醇聚氧乙烯醚硫酸铵(KD SE-10)通过低温乳液聚合法制备无皂丁腈橡胶.详细考察了可聚合乳化剂用量对门尼粘度、结合丙烯腈含量、凝胶量、拉伸强度、相对分子质量的影响情况,并确定了KD SE-10用量为2.7%~3.0%(质量分数).制得的无皂丁腈橡胶相比普通丁腈橡胶具有显著的高强度、更优良的耐油性、相对分子质量分布窄的特点.

  10. Role of cytochrome P450 2E1 in the metabolism of acrylamide and acrylonitrile in mice.

    Science.gov (United States)

    Sumner, S C; Fennell, T R; Moore, T A; Chanas, B; Gonzalez, F; Ghanayem, B I

    1999-11-01

    Acrylonitrile (AN) and acrylamide (AM) are commonly used in the synthesis of plastics and polymers. In rodents, AM and AN are metabolized to the epoxides glycidamide and cyanoethylene oxide, respectively. The aim of this study was to determine the role of cytochrome P450 in the metabolism of AM and AN in vivo. Wild-type (WT) mice, WT mice pretreated with aminobenzotriazole (ABT, 50 mg/kg ip, 2 h pre-exposure), and mice devoid of cytochrome P450 2E1 (P450 2E1-null) were treated with 50 mg/kg [(13)C]AM po. WT mice and P450 2E1-null mice were treated with 2.5 or 10 mg/kg [(13)C]AN po. Urine was collected for 24 h, and metabolites were characterized using (13)C NMR. WT mice excreted metabolites derived from the epoxides and from direct GSH conjugation with AM or AN. Only metabolites derived from direct GSH conjugation with AM or AN were observed in the urine from ABT-pretreated WT mice and P450 2E1-null mice. On the basis of evaluation of urinary metabolites at these doses, these data suggest that P450 2E1 is possibly the only cytochrome P450 enzyme involved in the metabolism of AM and AN in mice, that inhibiting total P450 activity does not result in new pathways of non-P450 metabolism of AM, and that mice devoid of P450 2E1 do not excrete metabolites of AM or AN that would be produced by oxidation by other cytochrome P450s. P450 2E1-null mice may be an appropriate model for the investigation of the role of oxidative metabolism in the toxicity or carcinogenicity of these compounds.

  11. Bacterial colonization and endotoxin content of a new renal dialysis water system composed of acrylonitrile butadiene styrene.

    Science.gov (United States)

    du Moulin, G C; Coleman, E C; Hedley-Whyte, J

    1987-06-01

    We measured endotoxin and bacterial levels in tap water, in water purified by reverse osmosis, and in dialysate samples over a 4-month period in a new 10-bed renal dialysis unit. Water treated by reverse osmosis is conducted to the 10 stations through 111 m of piping composed of acrylonitrile butadiene styrene (ABS). All determinations were made prior to the opening of the unit and after the system was purged for 35 h with all bedside station taps open. Formaldehyde disinfection of the piping system was attempted with a recommended protocol after 11 weeks by feeding 2.5 liters of 37% formaldehyde (0.85%, vol/vol) into the delivery system. Prior to water purging, 24 ng of endotoxin per ml was detected. This level decreased to 2.0 ng of endotoxin after the purging. Levels of endotoxin remained below 1.0 ng of endotoxin per ml throughout the duration of the study. In contrast, the level of viable microorganisms recovered from the treated water was approximately 3.5 X 10(4) CFU/100 ml. Even after disinfection of the system, there was no significant decrease in culturable bacteria from the water even though endotoxin levels were lower. Species isolated from the renal dialysis system were predominately pseudomonads, whereas species isolated from the tap water were Bacillus and Flavobacterium species. ABS provides a surface suitable for long-term colonization and growth of bacteria. Currently recommended decontamination protocols are ineffective in removing potentially pathogenic bacteria from ABS pipes and thus constitute an increased risk to patients undergoing dialysis.

  12. Simultaneous quantitation of urinary cotinine and acrylonitrile-derived mercapturic acids with ultraperformance liquid chromatography-tandem mass spectrometry.

    Science.gov (United States)

    Wu, Chia-Fang; Uang, Shi-Nian; Chiang, Su-Yin; Shih, Wei-Chung; Huang, Yu-Fang; Wu, Kuen-Yuh

    2012-02-01

    Acrylonitrile (AN), a widely used industrial chemical also found in tobacco smoke, has been classified as a possible human carcinogen (group 2B) by the International Agency for Research on Cancer. AN can be detoxified by glutathione S-transferase (GST) to form glutathione (GSH) conjugates in vivo. It can be metabolically activated by cytochrome P450 2E1 to form 2-cyanoethylene oxide, which can also be detoxified by GST to generate GSH conjugates. The GSH conjugates can be further metabolized to mercapturic acids (MAs), namely, N-acetyl-S-(2-cyanoethyl)cysteine (CEMA), N-acetyl-S-(2-hydroxyethyl)cysteine (HEMA), and N-acetyl-S-(1-cyano-2-hydroxyethyl)cysteine (CHEMA). This study developed an ultraperformance liquid chromatography coupled with tandem mass spectrometry (UPLC-MS/MS) method to quantitatively profile the major AN urinary metabolites (CEMA, HEMA, and CHEMA) to assess AN exposure, as well as analyze urinary cotinine (COT) as an indicator for tobacco smoke exposure. The limits of quantitation were 0.1, 0.1, 1.0, and 0.05 μg/L for HEMA, CEMA, CHEMA, and COT, respectively. This method was applied to analyze the three AN-derived MAs in 36 volunteers with no prior occupational AN exposure. Data analysis showed significant correlations between the level of COT and the levels of these MAs, suggesting them as biomarkers for exposure to low levels of AN. The results demonstrate that a highly specific and sensitive UPLC-MS/MS method has been successfully developed to quantitatively profile the major urinary metabolites of AN in humans to assess low AN exposure.

  13. Removal of As(V), Cr(III) and Cr(VI) from aqueous environments by poly(acrylonitril-co-acrylamidopropyl-trimethyl ammonium chloride)-based hydrogels.

    Science.gov (United States)

    Dudu, Tuba Ersen; Sahiner, Mehtap; Alpaslan, Duygu; Demirci, Sahin; Aktas, Nahit

    2015-09-15

    Cationic poly(Acrylonitril-co-Acrylamidopropyl-trimethyl Ammonium Chloride) (p(AN-co-APTMACl)) hydrogels in bulk were synthesized by using acrylonitrile (AN) and 3-acrylamidopropyl-trimethyl ammonium chloride (APTMACl) as monomers. The prepared hydrogels were exposed to amidoximation reaction to replace hydrophobic nitrile groups with hydrophilic amidoxime groups that have metal ion binding ability. Those replacements were increased the hydrogels absorption capacity for As(V) and Cr(VI). Langmuir and Freundlich isotherms equations were utilized to obtain the best-fitted isotherm model for the absorption of the ions at different metal ion concentrations. The absorption data of As(V) ion were fitted well to Freundlich isotherm while those of Cr(VI) and Cr(III) ions were fitted well to Langmuir isotherm. The maximum absorption of poly(3-acrylamidopropyl-trimethyl ammonium chloride (p(APTMACl)) and amid-p(AN-co-APTMACl) macro gels were 22.39 mg and 21.83 mg for As(V), and 30.65 mg and 18.16 mg for Cr(VI) ion per unit gram dried gel, respectively. Kinetically, the absorption behaviors of Cr(III) and Cr(VI) ions were fitted well to a pseudo 2nd-order kinetic model and those of As(V) ions were fitted well to a pseudo 1st order kinetic model.

  14. Spatial distribution of stabilizer-derived nitroxide radicals during thermal degradation of poly(acrylonitrile-butadiene-styrene) copolymers: a unified picture from pulsed ELDOR and ESR imaging.

    Science.gov (United States)

    Jeschke, Gunnar; Schlick, Shulamith

    2006-09-21

    Double Electron-Electron Resonance (DEER) provides information on the spatial distribution of radicals on the length scale of a few nanometres, while Electron Spin Resonance Imaging (ESRI) provides information on a length scale of millimetres with a resolution of about 100 micrometres. Despite the gap between these length scales, results from the two techniques are found to complement and support each other in the characterization of the identity and distribution of nitroxide radicals derived from the Hindered Amine Stabilizer (HAS) Tinuvin 770 in poly(acrylonitrile-butadiene-styrene) (ABS) copolymers. DEER measurements demonstrate that there is no significant formation of biradicals from the bifunctional HAS, and provide the distributions of local radical concentrations. These distributions are poorly resolved for model-free analysis of the DEER data by the Tikhonov regularization; the resolution was significantly improved by utilizing information obtained by ESRI. DEER data can be fitted with only one adjustable parameter, namely the average radical concentration, if 1D and 2D spectral--spatial ESRI results on both the spatial distribution of nitroxides and their distribution between the acrylonitrile--styrene-rich (SAN) and butadiene-rich (B) microphases are considered.

  15. Synthesis of novel well-defined poly(vinyl acetate)-b-poly(acrylonitrile) and derivatized water-soluble poly(vinyl alcohol)-b-poly(acrylic acid) block copolymers by cobalt-mediated radical polymerization

    NARCIS (Netherlands)

    Debuigne, A.; Warnant, J.; Jerome, R.; Voets, I.K.; Keizer, de A.; Cohen Stuart, M.A.; Detrembleur, C.

    2008-01-01

    Poly(vinyl acetate)¿Co(acac)2 macroinitiators, prepared by cobalt-mediated radical polymerization of vinyl acetate (VAc), were used to synthesize well-defined poly(vinyl acetate)-b-poly(acrylonitrile) (PVAc-b-PAN) block copolymers. Different solvents and temperatures were tested for the polymerizati

  16. Effect of ultrasound in the free radical polymerization of acrylonitrile under a new multi-site phase-transfer catalyst - a kinetic study.

    Science.gov (United States)

    Selvaraj, Varathan; Sakthivel, Perumal; Rajendran, Venugopal

    2015-01-01

    The kinetics of polymerization of acrylonitrile (AN) was carried out under heterogeneous condition using a new multi-site phase-transfer catalyst (MPTC), viz., N,N'-dihexyl-4,4'-bipyridinium dibromide in the presence of water soluble initiator, potassium peroxydisulphate (PDS) under chlorobenzene/water two phase system assisted by ultrasound irradiation at constant temperature 60+1°C under nitrogen atmosphere. The rate of polymerization increases with an increasing the concentrations of AN, MPTC and PDS. The order with respect to [AN], [MPTC], and [PDS] were found to be 1.01, 1.03 and 0.52, respectively. Based on the observed results a suitable mechanism has been proposed to account for the experimental observations followed by a discussion on its significance.

  17. One-step Preparation and Antibacterial Property of Poly(N-iso- propyl-acrylamide) Grafted Poly(acrylonitrile/styrene) Micro- spheres Immobilized with Silver Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    FENG,Jiao; FAN,Liheng; CHU,Hong; XIONG,Wanbin; JIANG,Jinqiang; CHEN,Mingqing

    2009-01-01

    Monodispersed silver nanoparticles were immobilized onto the surface of poly(N-isopropylacrylamide) grafted poly(acrylonitrile/styrene) (PNIPAAm-g-PAN/PSt) microspheres by a one-step method using AgNO3 as a silver source. This process was performed via the coordination interaction between Ag ions and amide groups on PNIPAAm-g-PAN/PSt microsphere surfaces with the reduction of the corresponding ions by ethanol taking place simultaneously. Fourier transform infrared (FTIR) spectroscopy and ultraviolet (UV)-visible spectra illustrated that the silver nanoparticles were successfully immobilized onto the PNIPAAm-g-PAN/PSt microspheres. The size and morphology of silvered microspheres were characterized by transmission electron microscopy (TEM). The weight percent of silver nanoparticles immobilized onto the microspheres was 12% based on the determination of thermogravimetric analysis (TGA). The antibacterial tests demonstrated that the as-prepared silvered microspheres showed activity against Gram-negative bacteria.

  18. FINITE ELEMENT SIMULATION FOR YIELD STRESS OF HARD POLY(VINYL CHLORIDE)/ACRYLONITRILE-BUTADIENE-STYRENE BLENDS AT DIFFERENT CROSSHEAD SPEEDS

    Institute of Scientific and Technical Information of China (English)

    Pei-hua Du; Jie Yu; Peng-fei Lin; Yi-hu Song; Qiang Zneng

    2011-01-01

    Hard poly(vinyl chloride) (PVC)/acrylonitrile-butadiene-styrene (ABS) blends were prepared using injectionmolding and influence of crosshead speed on mechanical properties was examined.Based on morphology parameters obtained from transmission electron microscopy photography and the material parameters from true stress-strain curves of neat PVC and ABS,yield stresses of the blends at different crosshead speeds were simulated employing a two-dimensional nine-particle model based on the finite element analysis (FEA).The FEA results were compared with the experimental yielding stress and the good agreement validated the simulation approach.The FEA approach allowed establishing a yielding criterion related to local yielding of the interstitial matrix between ABS particles.

  19. Studies on blends of cycloaliphatic epoxy resin with varying concentrations of carboxyl terminated butadiene acrylonitrile copolymer I: Thermal and morphological properties

    Indian Academy of Sciences (India)

    Garima Tripathi; Deepak Srivastava

    2009-04-01

    Differential scanning calorimetric (DSC), thermogravimetric analysis (TGA) and dynamic mechanical analysis (DMA) of the blends of cycloaliphatic epoxy (CAE) resin toughened with liquid elastomer such as carboxyl terminated butadiene acrylonitrile copolymer (CTBN) have been carried out. Exothermal heat of reaction due to cross linking of the resin in the presence of diamino diphenyl sulphone (DDS, an amine hardener) showed a decreasing trend with increasing rubber concentration. Enhancement of thermal stability as well as lower mass loss of the epoxy–rubber blends with increasing rubber concentration have been observed in thermogravimetric analysis (TGA). Dynamic mechanical properties reflected a monotonic decrease in the storage modulus (′) with increasing rubber concentration. The loss modulus (″) and the loss tangent (tan ) values, however, showed an increasing trend with rise of temperature up to a maximum (peak) followed by a gradual fall in both cases.

  20. Thermosensitive Poly(N-isopropylacrylamide-co-acrylonitrile) Hydrogels with Rapid Response%非离子型凝胶球在水中的溶胀行为

    Institute of Scientific and Technical Information of China (English)

    黄健; 黄志明; 包永忠; 翁志学

    2006-01-01

    Acrylonitrile (AN) was copolymerized with N-isopropylacrylamide (NIPA) to synthesize thermosensitive bydrogels, and the on-off switch behavior of poly(NIPA-co-AN) hydrogels with different fraction of hydrophobic component (AN) was investigated. It is found that the lower critical solution temperature (LCST), the swelling ratio at certain temperature and the reswelling rate of poly(NIPA-co-AN) hydrogels decreased as AN unit fraction in copolymers increased. In order to improve the responsive rate of poly(NIPA-co-AN) hydrogels, they were further treated by surface crosslinking using N, N'-methylene bisacrylamide (BIS) as a crosslinking agent. The swelling and deswelling behaviors of these copolymers were compared with those of the untreated hydrogels. The results indicated that the responsive rate of poly(NIPA-co-AN) hydrogel was improved by surface crosslinking. The resulting hydrogels bearing cyano groups with fast response have potential applications in the field of drug-controlled release and immobilization of biomolecules.

  1. Modification on liquid retention property of cassava starch by radiation grafting with acrylonitrile. I. Effect of γ-irradiation on grafting parameters

    Science.gov (United States)

    Kiatkamjornwong, S.; Chvajarernpun, J.; Nakason, C.

    1993-07-01

    Radiation modification on liquid retention properties of native cassava starch, gelatinized at 85°C, by graft copolymerization with acrylonitrile was carried out by mutual irradiation to gamma-rays. A thin aluminum foil was used to cover the inner wall of the reaction vessel, so that the homopolymer concentration was reduced to be less than 1.0% with a distilled water retention value of 665 g/g of the dry weight of the saponified grafted product. Confirmation of graft copolymerization and saponification reactions was made by the infrared spectrophotometric technique. The combined effect of radiation parameters in terms of an irradiation time and a dose rate to the total dose on the extent of the grafting reaction expressed in terms of grafting parameters which directly influenced liquid retention values was evaluated in conjunction with statistical analysis.

  2. NIOSH (National Institute for Occupational Safety and Health) testimony to DOL (Department of Labor) on occupational exposure to acrylonitrile, by R. Yodaiken, M. D. , March 3, 1978

    Energy Technology Data Exchange (ETDEWEB)

    1978-03-03

    Testimony was presented concerning the establishment of an occupational exposure standard for acrylonitrile (AN) to which an estimated 125,000 workers were potentially exposed. Two-year feeding and inhalation studies with animals indicated the chemical to be carcinogenic, producing tumors of the central nervous system (CNS), cerebral tumors, squamous cell neoplasms of the Zymbal gland, adenocarcinoma of the small intestine and large intestine, along with numerous benign tumors. Other findings included papillomata in the stomach, hemangioma of the kidney, fibroadenomas of the mammary gland, benign tumors of the uterus, and tumors of the ear canal. Teratogenicity studies indicated increased incidence of fetal malformation. Cases of AN as an allergen causing contact dermatitis and ulcers have been widely documented. It was recommended that drugs essential to the treatment of acute intoxication from AN be kept in the medical facility of all facilities using AN, and that employers institute a respiratory-protection program in accordance with requirements.

  3. SELECTIVE SEPARATION OF WATER-ETHANOL MIXTURES THROUGH COPOLYMERIC MEMBRANES:Ⅰ. ACRYLIC ACID AND ACRYLONITRILE COPOLYMER AND ITS IONIZED MEMBRANES

    Institute of Scientific and Technical Information of China (English)

    ZHANG Fuyao; ZHANG Yifeng; ZHAO Zhuomin; SHEN Zhiquan

    1993-01-01

    The copolymer of acrylic acid and acrylonitrile has been synthesized and pervaporation properties of the copolymeric membranes have been investigated. In order to elucidate the influence of membrane-permeate interaction on the pervaporation of water-ethanol mixtures and to prepare much improved membranes, the membranes have been treated with alkali metal, alkali earth metal and transition metal salt aqueous solutions. The treated membranes (ionized membranes)exhibited higher separation factors than the untreated membranes. The separation factors of various alkali metal cation membranes decreased in the following order: Li+>Na+>K+, and the permeation rates showed an opposite tendency. The dependence of pervaporation behavior on the copolymer composition ,feed concentration and operating temperature have been studied with both ionized and non-ionized membranes. The apparent activation energies of water and ethanol permeation were calculated.

  4. 光照射下丙烯腈活性自由基聚合的研究%Photo-induced Living Radical Polymerization of Acrylonitrile

    Institute of Scientific and Technical Information of China (English)

    何斌鸿

    2015-01-01

    Acrylonitrile as monomer, azobisisobutyronitrile as initiator, hexamethylenetetramine as ligand, copper chloride dihydrate as catalyst and Vitamin C as reducing agent, polyacrylonitrile was synthesized in N,N-dimethylformamide under the light irradiation. The effects of the amount of monomer, initiator, catalyst, hexamethylenetetramine and Vitamin C on the photo-induced polymerization of acrylonitrile have been invetigated. On the basis of experiments, it is concluded that the best polymerization conditions were that the amount of monomer is 0.2 mol and the usage of azobisisobutyronitrile, copper chloride dihydrate, hexamethylenetetramine and vitamin C was 1%, 0.75%, 1%, 4 % of the mole of monomer, respectively. The best reaction time is 11 h.%以丙烯腈作为单体,偶氮二异丁腈为引发剂,六次亚甲基四胺为配体,二水氯化铜为催化剂,维生素C为还原剂,在光的照射下,于溶剂 N,N-二甲基甲酰胺中采用自由基聚合的原理制得聚丙烯腈,并探究改变单一反应物的用量时对该聚合反应的影响,最后得出最佳的聚合条件为:在室温20℃下反应时,最佳单体用量为0.2mol,引发剂偶氮二异丁腈、催化剂二水氯化铜、配体六次亚甲基四胺、还原剂维生素C分别为单体摩尔总量的1%、0.75%、1%、4%,最佳反应时间为11 h.

  5. Study on Secondary Pollutant Emissions from Incineration of Acrylonitrile Waste Water%丙烯腈废液焚烧二次污染物排放的特性研究

    Institute of Scientific and Technical Information of China (English)

    陈高; 李传凯

    2012-01-01

    The experiment of acrylonitrile waste water incineration are carried out to investigate the influence rule of secondary pollutant CO, NOx emissions by changing the incineration temperature, residence time of incineration, the oxygen content of furnace on acrylonitrile waste water incinerator test apparatus.%在废液焚烧炉实验台上进行丙烯腈废液焚烧实验,通过改变废液焚烧温度、焚烧停留时间、烟气中氧含量等参数,研究分析各种因素对丙烯腈废液焚烧二次污染物CO、NOx排放的影响规律.

  6. A method for the quantification of biomarkers of exposure to acrylonitrile and 1,3-butadiene in human urine by column-switching liquid chromatography-tandem mass spectrometry.

    Science.gov (United States)

    Schettgen, T; Musiol, A; Alt, A; Ochsmann, E; Kraus, T

    2009-02-01

    1,3-Butadiene and acrylonitrile are important industrial chemicals that have a high production volume and are ubiquitous environmental pollutants. The urinary mercapturic acids of 1,3-butadiene and acrylonitrile-N-acetyl-S-(3,4-dihydroxybutyl)cysteine (DHBMA) and MHBMA (an isomeric mixture of N-acetyl-S-((1-hydroxymethyl)-2-propenyl)cysteine and N-acetyl-S-((2-hydroxymethyl)-3-propenyl)cysteine) for the former and N-acetyl-S-2-cyanoethylcysteine (CEMA) for the latter-are specific biomarkers for the determination of individual internal exposure to these chemicals. We have developed and validated a fast, specific, and very sensitive method for the simultaneous determination of DHBMA, MHBMA, and CEMA in human urine using an automated multidimensional LC/MS/MS method that requires no additional sample preparation. Analytes are stripped from urinary matrix by online extraction on a restricted access material, transferred to the analytical column, and subsequently determined by tandem mass spectrometry using labeled internal standards. The limits of quantification (LOQs) for DHBMA, MHBMA, and CEMA were 10 microg/L, 2 microg/L, and 1 microg/L urine, respectively, and were sufficient to quantify the background exposure of the general population. Precision within series and between series for all analytes ranged from 5.4 to 9.9%; mean accuracy was between 95 and 115%. We applied the method on spot urine samples from 210 subjects from the general population with no occupational exposure to 1,3-butadiene or acrylonitrile. A background exposure of the general population to acrylonitrile was discovered that is basically influenced by individual exposure to passive smoke as well as active smoking habits. Smokers showed a significantly higher excretion of MHBMA, whereas DHBMA levels did not differ significantly. Owing to its automation, our method is well suited for application in occupational or environmental studies.

  7. 顶空-气相色谱法测定水中乙醛、丙烯醛和丙烯腈%Determination of Acetaldehyde,Acrylaldehyde and Acrylonitrile in Water with Headspace Gas Chromatography

    Institute of Scientific and Technical Information of China (English)

    何芸菁

    2013-01-01

    A headspace gas chromatography method was developed for acetaldehyde, acrylaldehyde and acrylonitrile in water. This method shows good separating effect and high sensitivity. The lowest detection limits were 0.03mg/L for acetaldehyde, 0.07mg/L for acrylaldehyde , 0.04mg/L for acrylonitrile. The recovery rates were 86% ~115% for acetaldehyde, 81%~110%for acrylaldehyde , 80%~108%for acrylonitrile. Experiment results show that the advantages of this method are simple, rapid, accurate for determination of acetaldehyde, acrylaldehyde and acrylonitrile in surface water and wastewater.%建立了顶空-气相色谱法测定水中乙醛、丙烯醛和丙烯腈的分析方法。该方法分离度好,灵敏度高,水中乙醛、丙烯醛和丙烯腈的检出浓度为0.03mg/L、0.07mg/L、0.04mg/L,回收率分别为86%~115%、81%~110%、80%~108%。结果表明,顶空-气相色谱法测定水中乙醛、丙烯醛和丙烯腈方法简单快捷,准确,适合地表水、废水中乙醛、丙烯醛和丙烯腈的同时测定。

  8. 顶空气相色谱法同时测定水中乙醛、丙烯醛和丙烯腈%Determination of Acetaldehyde, Acrylaldehyde and Acrylonitrile in Water with Headspace Gas Chromatography

    Institute of Scientific and Technical Information of China (English)

    於香湘; 缪建军; 吴鹏; 项徐伟

    2011-01-01

    A headspace gas chromatography method was developed for the simultaneous determination of acetaldehyde,acrylaldehyde and acrylonitrile in water. Acetaldehyde, acrylaldehyde and acrylonitrile in water samples were extracted by headspace technology,then seperated with HP-innowax capillary column and detected by FID. Retention time of the peaks was used for qualitative analysis,while external standard method was used for quantitative analysis. The lowest detection limits were 0.04 mg/L for acetaldehyde, 0.02 mg/L for acrylaldehyde and 0.01 mg/L for acrylonitrile. The recovery rates were 95.2% ~ 98.7% for acetaldehyde, 95.8% ~ 97.9% for acrylaldehyde and 96.7% ~ 99.6% for acrylonitrile. And RSD (n = 6)were lower than 5.2%. This method is simple, rapid, accurate and applicable for determination of acetaldehyde,acrylaldehyde and acrylonitrile in various water samples.%建立水中微量乙醛、丙烯醛和丙烯腈的顶空气相色谱(HS-GC)测定方法,经项空进样,用HP-INNOWAX毛细管色谱柱程序升温分离,FID检测,以保留时间定性,外标法定量.水中乙醛、丙烯醛和丙烯腈的检出质量浓度分别为0.04,0.02和0.01 mg/L.样品加标回收率乙醛为952%~98.7%,丙烯醛为95.8%~97.9%,丙烯腈为96.7%~99.6%,6次平行测定结果的相对标准差不大于5.2%.该方法简便、快速、准确、重现性好,适合各种水中乙醛、丙烯醛和丙烯腈的同时测定.

  9. Evaluation of image uniformity and radiolucency for computed tomography phantom made of 3-dimensional printing of fused deposition modeling technology by using acrylonitrile but audience styrene resin

    Energy Technology Data Exchange (ETDEWEB)

    Seoung, Youl Hun [Dept. of of Radiological Science, Cheongju University, Cheongju (Korea, Republic of)

    2016-09-15

    The purpose of this study was to evaluate the radiolucency for the phantom output to the 3D printing technology. The 3D printing technology was applied for FDM (fused deposition modeling) method and was used the material of ABS (acrylonitrile butadiene styrene) resin. The phantom was designed in cylindrical uniformity. An image uniformity was measured by a cross-sectional images of the 3D printed phantom obtained from the CT equipment. The evaluation of radiolucency was measured exposure dose by the inserted ion-chamber from the 3D printed phantom. As a results, the average of uniformity in the cross-sectional CT image was 2.70 HU and the correlation of radiolucency between PMMA CT phantom and 3D printed ABS phantom is found to have a high correlation to 0.976. In the future, this results will be expected to be used as the basis for the phantom production of the radiation quality control by used 3D printing technology.

  10. Microwave absorption properties of lightweight absorber based on Fe50Ni50-coated poly(acrylonitrile) microspheres and reduced graphene oxide composites

    Science.gov (United States)

    Zhang, Bin; Wang, Jun; Wang, Junpeng; Huo, Siqi; Zhang, Bin; Tang, Yushan

    2016-09-01

    In this paper, we proposed a facile method to obtain the lightweight composites consisting of surface modified Fe50Ni50-coated poly(acrylonitrile) microspheres (PANS@SMF), reduced graphene oxide (RGO) and epoxy resin. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), vibrating sample magnetometry (VSM) and vector network analyzer (VNA). Impedance matching condition and electromagnetic wave attenuation characteristic were used for the reflection loss (RL) performance of the composites. Compared with pure PANS@SMF and RGO composites, the -10 dB absorption bandwidth and the minimum RL of the hybrid composites were enhanced. The bandwidth less than -10 dB was almost 4.5 GHz in the range of 10 GHz to 14.5 GHz, with a matching thickness of 2.5 mm. The density of the hybrid composites was in the range of 0.25-0.34 g/cm3. Therefore, the hybrid composite can be considered as a potential lightweight microwave absorber.

  11. Mechanistic insight into selective catalytic combustion of acrylonitrile (C2H3CN): NCO formation and its further transformation towards N2.

    Science.gov (United States)

    Liu, Ning; Yuan, Xiaoning; Zhang, Runduo; Xu, Rongrong; Li, Yingxia

    2017-03-15

    A series of zeolite catalysts, M(Cu, Fe, Co)-ZSM-5, was prepared by an impregnation method and evaluated for the selective catalytic combustion of acrylonitrile (AN-SCC). Cu-ZSM-5, exhibiting the highest AN conversion activity and best N2 yield, was further selected for an AN-SCC mechanism investigation, wherein both experimental [in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS)] and theoretical [density functional theory (DFT)] approaches were employed. The in situ DRIFTS revealed that AN-SCC followed a hydrolysis mechanism at T 300 °C via an intermediate of NCO. The DFT simulations gave much deeper insights suggesting that: (i) the NCO could be generated by oxidation of AN over [Cu](+) active sites, with an assistance of dissociated atomic O from gaseous O2; (ii) three types of reaction routes could be proposed for the further reaction of NCO to produce N2, namely NCO direct dissociation, NCO coupling, and NO + NCO reaction; and (iii) the last route (NO + NCO), possessing the lowest energy barrier, was the most probable reaction pathway, wherein the NO could be produced by oxidation of NCO. The DFT energy calculation results and microkinetic analyses revealed that the NCO generation step, possessing an energy barrier of 17.0 kcal mol(-1) and a forward reaction rate constant of 2.20 × 10(7) s(-1), was the rate-determining step of the whole catalytic cycle.

  12. Three-dimensional Printed Acrylonitrile Butadiene Styrene Framework Coated with Cu-BTC Metal-organic Frameworks for the Removal of Methylene Blue

    Science.gov (United States)

    Wang, Zongyuan; Wang, Jiajun; Li, Minyue; Sun, Kaihang; Liu, Chang-Jun

    2014-08-01

    Three-dimensional (3D) printing was applied for the fabrication of acrylonitrile butadiene styrene (ABS) framework. Functionalization of the ABS framework was then performed by coating of porous Cu-BTC (BTC = benzene tricarboxylic acid) metal-organic frameworks on it using a step-by-step in-situ growth. The size of the Cu-BTC particles on ABS was ranged from 200 nm to 900 nm. The Cu-BTC/ABS framework can take up most of the space of the tubular reactor that makes the adsorption effective with no need of stirring. Methylene blue (MB) can be readily removed from aqueous solution by this Cu-BTC/ABS framework. The MB removal efficiency for solutions with concentrations of 10 and 5 mg/L was 93.3% and 98.3%, respectively, within 10 min. After MB adsorption, the Cu-BTC/ABS composite can easily be recovered without the need for centrifugation or filtration and the composite is reusable. In addition the ABS framework can be recovered for subsequent reuse. A significant advantage of 3D-printed frameworks is that different frameworks can be easily fabricated to meet the needs of different applications. This is a promising strategy to synthesize new frameworks using MOFs and polymers to develop materials for applications beyond adsorption.

  13. Co-recycling of acrylonitrile-butadiene-styrene waste plastic and nonmetal particles from waste printed circuit boards to manufacture reproduction composites.

    Science.gov (United States)

    Sun, Zhixing; Shen, Zhigang; Zhang, Xiaojing; Ma, Shulin

    2015-01-01

    This study investigated the feasibility of using acrylonitrile-butadiene-styrene (ABS) waste plastic and nonmetal particles from waste printed circuit boards (WPCB) to manufacture reproduction composites (RC), with the aim of co-recycling these two waste resources. The composites were prepared in a twin-crew extruder and investigated by means of mechanical testing, in situ flexural observation, thermogravimatric analysis, and dimensional stability evaluation. The results showed that the presence of nonmetal particles significantly improved the mechanical properties and the physical performance of the RC. A loading of 30 wt% nonmetal particles could achieve a flexural strength of 72.6 MPa, a flexural modulus of 3.57 GPa, and an impact strength of 15.5 kJ/m2. Moreover, it was found that the application of maleic anhydride-grafted ABS as compatilizer could effectively promote the interfacial adhesion between the ABS plastic and the nonmetal particles. This research provides a novel method to reuse waste ABS and WPCB nonmetals for manufacturing high value-added product, which represents a promising way for waste recycling and resolving the environmental problem.

  14. Study on ion conductivity and crystallinity of composite polymer electrolytes based on poly(ethylene oxide)/poly(acrylonitrile) containing nano-sized Al2O3 fillers.

    Science.gov (United States)

    Kim, Mingyeong; Lee, Lyungyu; Jung, Yongju; Kim, Seok

    2013-12-01

    In this paper, composite polymer electrolytes were prepared by a blend of poly(ethylene oxide) (PEO) and poly(acrylonitrile) (PAN) as a polymer matrix, ethylene carbonate as a plasticizer, LiClO4 as a salt, and by containing a different content of nano-sized Al2O3. The composite films were prepared by using the solution casting method. The crystallinity and ionic conductivity of the polymer electrolytes was investigated using X-ray diffraction (XRD) and AC impedance method, respectively. The morphology of composite polymer electrolyte film was analyzed by SEM method. From the experimental results, by increasing the Al2O3 content, the crystallinity of PEO was reduced, and the ionic conductivity was increased. In particular, by a doping of 15 wt.% Al2O3 in PEO/PAN polymer blend, the CPEs showed the superior ionic conductivity. However, when Al2O3 content exceeds 15 wt.%, the ionic conductivity was decreased. From the surface morphology, it was concluded that the ionic conductivity was decreased because the CPEs showed a heterogenous morphology due to immiscibility or aggregation of the ceramic filler within the polymer matrix.

  15. Preparation and Characterization of Carboxyl-terminated Poly (butadiene-co-acrylonitrile)-epoxy Resin Prepolymers for Fusion-bonded-epoxy Powder Coating

    Institute of Scientific and Technical Information of China (English)

    LIU Jingcheng; JIA Xiuli; ZHANG Shengwen; LIU Ren; LIU Xiaoya

    2012-01-01

    Liquid carboxyl-terminated poly(butadiene-co-acrylonitrile)(CTBN)-epoxy resin(EP)prepolymers were prepared with different contents of CTBN.The chemical reactions between EP and CTBN were characterized by Fourier ransform infrared (FTIR) spectroscopy and gel permeation chromatography (GPC).The scanning electron micrograph (SEM) and dynamic mechanical analysis (DMA) of curing films showed phase separation,and the rubber particles were finely dispersed in the epoxy matrix.Mechanical properties analysis of curing films showed that impact strength and elongation at break increased significantly upon the addition of CTBN,indicating good toughness of the modified epoxy resins.Thermogravimetric analysis (TGA) showed that the incorporation of CTBN had little effect on the thermal stability of EP.Fusion-bondedepoxy (FBE) powder coatings modified with CTBN-EP prepolymers were prepared.The experimental results demonstrate the ability of CTBN-EP prepolymers,toughening technology to dramatically enhance the flexibility and impact resistance of FBE coatings without compromising other key properties such as corrosion protection.

  16. Poly(acrylonitrile-co-butadiene-co-styrene Reinforced with Hollow Glass Microspheres: Evaluation of Extrusion Parameters and Their Effects on the Composite Properties

    Directory of Open Access Journals (Sweden)

    Marina Panozzo Cunha

    2016-01-01

    Full Text Available Hollow glass microspheres (HGMs filled poly(acrylonitrile-co-butadiene-co-styrene (ABS composites were prepared by means of a twin-screw extruder. S038 HGMs were incorporated at different percentages of 2.5, 5.0, and 7.5 wt%. The HGMs were added into the twin-screw extruder at two different feeding zones, and the effect of HGMs loading and specific feeding zone addition on the composites produced was evaluated with regard to morphological, thermal, rheological, physical, and mechanical properties. As a result, the composite density was reduced while the thermal stability, storage modulus, complex viscosity, and tensile and flexural modulus were improved when compared with the ABS matrix. The results also indicate that the addition of 5.0 wt% of HGMs at the feeding zone closer to the die maintains the integrity of the HGMs and promotes composites with higher mechanical properties and lower density when compared with the composites obtained with the addition of HGMs closer to the hopper.

  17. Molecular Structure and Crystal Packing of n-Type Semiconducting Material 3′,3′-(1,4-Phenylene)bis{2′-(4′′-trifluoromethyl)phenyl}acrylonitrile

    OpenAIRE

    Tetsuji Moriguchi; Shuichi Nagamatsu; Tatsuo Okauchi; Akihiko Tsuge; Wataru Takashima; Shuji Hayase

    2014-01-01

    The exact molecular structure and the crystal packing of the n-type semiconducting material 3′,3′-(1,4-phenylene)bis{2′-(4′′-trifluoromethyl)phenyl}acrylonitrile was determined by a single crystal X-ray diffraction with twin treatment technique. The air-stable product was crystallized from dichloromethane-hexane mixed solution. The solid-state structure is the example of a typical π-π stacking with side intermolecular CN–H short contact networks.

  18. Simultaneous determination of acrylonitrile and trichloroethylene in the air of workplace by gas chromatography%气相色谱法同时测定工作场所空气中的丙烯腈和三氯乙烯

    Institute of Scientific and Technical Information of China (English)

    刘云富; 谭广辉

    2013-01-01

    Objective: To establish a method for the simultaneous determination of acrylonitrile and trichloroethyl-ene in the air of workplace by gas chromatography. Methods: Acrylonitrile and trichloroethylene in the air of workplace were collected with charcoal tube, then desorbed with carbon disulfide, and finally separated with a Rtx(R) -Wax capillary column (30 m ×0. 25 mm ×0. 25 μm) and detected with flame ionization detector. Results: The linearity ranges were 0.5 μg/ml ~200 μg/ml,2.6 μg/ml ~250 μg/ml for acrylonitrile and trichloroethylene, respectively. The coefficients of correlation were 0. 9999, 0. 9992 and the limits of detection were 0. 5 μg/ml and 2. 6 μg/ml. Conclusion: Separation effect of the two organic compounds was good, the method is suitable for determining acrylonitrile and trichloroethylene in the air of workplace simultaneously.%目的:建立工作场所空气中丙烯腈和三氯乙烯的气相色谱同时测定方法.方法:采用活性炭管吸附工作场所空气中丙烯腈和三氯乙烯,经二硫化碳解吸后进样,使用Rtx@-Wax毛细管柱(30 m×0.25 mm×0.25μm)分离和火焰离子化检测器检测.结果:丙烯腈、三氯乙烯的线性范围分别为0.5μg/ml ~200μg/ml和2.6 μg/ml ~ 250 μg/ml;相关系数分别为0.9999和0.9992;检出限分别为0.5 μg/ml和2.6 μg/ml,解吸效率分别为89%和95%,相对标准偏差为1.2% ~6.4%、0.9% ~4.7%.结论:该方法对两种物质的分离效果好,适合工作场所空气中丙烯腈和三氯乙烯的同时测定.

  19. Microwave absorption properties of lightweight absorber based on Fe{sub 50}Ni{sub 50}-coated poly(acrylonitrile) microspheres and reduced graphene oxide composites

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Bin [School of Material Science And Engineering, Wuhan University of Technology, Wuhan 430070 (China); Wang, Jun, E-mail: wgdfrp@whut.edu.cn [School of Material Science And Engineering, Wuhan University of Technology, Wuhan 430070 (China); Wang, Junpeng; Huo, Siqi [School of Material Science And Engineering, Wuhan University of Technology, Wuhan 430070 (China); Zhang, Bin [School of Science, Wuhan University of Technology, Wuhan 430070 (China); Tang, Yushan [School of Material Science And Engineering, Wuhan University of Technology, Wuhan 430070 (China)

    2016-09-01

    In this paper, we proposed a facile method to obtain the lightweight composites consisting of surface modified Fe{sub 50}Ni{sub 50}-coated poly(acrylonitrile) microspheres (PANS@SMF), reduced graphene oxide (RGO) and epoxy resin. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), vibrating sample magnetometry (VSM) and vector network analyzer (VNA). Impedance matching condition and electromagnetic wave attenuation characteristic were used for the reflection loss (RL) performance of the composites. Compared with pure PANS@SMF and RGO composites, the −10 dB absorption bandwidth and the minimum RL of the hybrid composites were enhanced. The bandwidth less than −10 dB was almost 4.5 GHz in the range of 10 GHz to 14.5 GHz, with a matching thickness of 2.5 mm. The density of the hybrid composites was in the range of 0.25–0.34 g/cm{sup 3}. Therefore, the hybrid composite can be considered as a potential lightweight microwave absorber. - Highlights: • PANS@SMF – RGO epoxy composite was fabricated by a facile method. • The absorption bandwidth less than −10 dB can reach up to 4.5 GHz with layer thickness of 2.5 mm. • The density of the composites is in the range of 0.25–0.34 g/cm{sup 3} and can be considered as a lightweight microwave absorber.

  20. Improvement in the etching performance of the acrylonitrile-butadiene-styrene resin by MnO2-H3PO4-H2SO4 colloid.

    Science.gov (United States)

    Zhao, Wenxia; Ding, Jie; Wang, Zenglin

    2013-05-21

    The present study aimed to evaluate the surface etching of the acrylonitrile-butadiene-styrene (ABS) resin in the MnO2-H3PO4-H2SO4 colloid. To enhance the soluble Mn(IV) ion concentration and improve the etching performance of ABS resin, H3PO4 was added as a complexing agent into the MnO2-H2SO4 etching system. The effects of the H2SO4 concentration and etching time on the surface topography, surface roughness, adhesion strength, and the surface chemistry of the ABS substrates were investigated. The optimal oxidation potentials of MnO2 in the colloids decreased from 1.426 to 1.369 V with the addition of H3PO4. Though the etching conditions changed from 70 °C for 20 min to 60 °C for 10 min, the adhesion strength between the ABS substrates and electroless copper film increased from 1.19 to 1.33 KN/m after etching treatment. This could be attributed to the significant increase of the soluble Mn(IV) ion concentration in the MnO2-H3PO4-H2SO4 colloid. The surface chemistry results demonstrated that the oxidation reaction of -C═C- bonds in the polybutadiene phase was accelerated in the etching process by the addition of H3PO4, and the abundant -COOH and -OH groups were formed rapidly on the ABS surface with the etching treatment. These results were in agreement with the results of surface scanning electron microscopic observations and adhesion strength measurement. The results suggested that the MnO2-H3PO4-H2SO4 colloid was an effective surface etching system for the ABS surface roughness.

  1. 丙烯腈吸收过程模拟优化%Simulation and Optimization of the Absorption Process to a Acrylonitrile Plant

    Institute of Scientific and Technical Information of China (English)

    杨家军; 霍凤华; 崔吉成

    2015-01-01

    Throughout its history,chemical process simulation software has been widely used in chemical process design,operational evaluation and optimization.As well known by chemical technicans,the PROII software was used for the simulation of the absorption process of acrylonitrile production plant in the study.Firstly,the operating parameters of the absorption process were analyzed to determine the optimization variables.After that, the absorption tower was simulated with PROII software.By comparing the simulation results of different conditions,the process parameters related to the sbsorption process were analyzed,such as the comsuption of absorption water and side withdrawing,and the operating pressure. The optimum values in the corresponding conditions were obtained.%化工过程模拟软件发展至今已被广泛地应用于化工过程的设计计算、操作评估和优化中。该文应用化工技术人员熟知的PROII软件对丙烯腈的吸收过程进行模拟研究。首先对年产20万吨的丙烯腈生产过程吸收塔单元中的操作参数进行分析,确定要优化的参数。然后应用PROII软件对丙烯腈吸收塔进行模拟,通过改变操作参数后模拟结果的比较对操作参数中的吸收水用量、侧线采出量和吸收塔的操作压力进行了模拟分析,并得到相应条件下的最佳值。

  2. Surface hydrophilic modification of acrylonitrile-butadiene-styrene terpolymer by poly(ethylene glycol-co-1,4-cyclohexanedimethanol terephthalate): Preparation, characterization, and properties studies

    Science.gov (United States)

    Chen, Tingting; Zhang, Jun

    2016-12-01

    Surface hydrophilic modified acrylonitrile-butadiene-styrene (ABS) terpolymer was prepared by melt blending with poly(ethylene glycol-co-1,4-cyclohexanedimethanol terephthalate) (PETG) random copolymer as the modifier. Attenuated total reflectance-Fourier transform-infrared spectroscopy (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS) were used for surface analysis. Through the contact angle measurement, the relationship between surface properties of the ABS/PETG blends and PETG content was investigated. Scanning electron microscope (SEM) and dynamical mechanical thermal analysis (DMTA) were used to characterize interface morphology and compatibility of the blends. The effect of PETG content on the mechanical and rheological properties was examined. The ATR-FTIR and XPS analysis suggested that the hydrophilic groups were enriched on the surface with increasing PETG content in the blend. The decrease of the water contact angle and the increase of the polarity for the blends with increasing PETG content indicated that the hydrophilic property of the blends was enhanced with increasing PETG content. The ABS/PETG blends were partially miscible. And the blends with ≤50 wt% PETG had better compatibility than the blends with above 50 wt% PETG. It was clear that below 50 wt% PETG, the PETG phase was dispersed in spherical form and the ABS phase was continuous. Above 50 wt% PETG, the PETG phase became continuous and the ABS phase was dispersed in irregular form. Moreover, the tensile strength and flexural strength of the blends were enhanced with increasing PETG content. The flexural modulus almost remained constant. And the impact strength was decreased when the content of PETG was increasing.

  3. 液体丁腈橡胶-26特性黏数快速测定%Rapid determination of intrinsic viscosity for liquid acrylonitrile-butadiene rubber-26

    Institute of Scientific and Technical Information of China (English)

    王真琴; 吴福生; 梁滔; 龚光碧

    2012-01-01

    The intrinsic viscosity of liquid acrylonitrile-butadiene rubber - 26 was determined by dilution method with acetone as solvent,and the constants Κ,Β in Huggins and Kraemer equations were calculated. When Κ and Β met 0.180≤Κ≤0. 472,Κ+β≈0.5, the rapid method could be used to calculate intrinsic viscosity of liquid acrylonitrile - butadiene rubber -26. The relative error and the standard deviation of the rapid method were less than 3% ,0. 150%respectively.%将液体丁腈橡胶-26溶解于丙酮中,采用稀释法测定试样的特性黏数,同时计算出Huggins 方程和Kraemer方程的κ,β常数,当二者满足0.180≤κ≤0.472,κ+β≈0.5,可以用快速法计算液体丁腈橡胶-26的特性黏数.结果表明,快速法相对误差小于3%,最大标准偏差小于0.150%.

  4. Simultaneous quantification of haemoglobin adducts of ethylene oxide, propylene oxide, acrylonitrile, acrylamide and glycidamide in human blood by isotope-dilution GC/NCI-MS/MS.

    Science.gov (United States)

    Schettgen, T; Müller, J; Fromme, H; Angerer, J

    2010-10-01

    Haemoglobin adducts are highly valuable biomarkers of cumulative exposure to carcinogenic substances. We have developed and applied an analytical method for the simultaneous quantification of five haemoglobin adducts of important occupational and environmental carcinogens. The N-terminal adducts were determined with gas chromatography as pentafluorophenylthiohydantoine derivatives according to the modified Edman-procedure and subsequent acetonization of the glycidamide adduct N-(R,S)-2-hydroxy-2-carbamoylethylvaline (GAVal). The use of self-synthesized labelled internal standards in combination with tandem mass spectrometry using negative chemical ionisation guarantees both high accuracy and sensitivity of our determination. The limit of detection for N-2-hydroxyethylvaline (HEVal), N-(R,S)-2-hydroxypropylvaline (HPVal), N-2-carbamoylethylvaline (AAVal) and N-(R,S)-2-hydroxy-2-carbamoylethylvaline (GAVal) was 2 pmol/g globin, for N-2-cyanoethylvaline (CEVal) it was determined as 0.5 pmol/g globin, which was sufficient to determine the background levels of these adducts in the non-smoking general population. The between-day-precision for all analytes using a human blood sample as quality control material ranged from 4.7 to 12.3%. We investigated blood samples of a small group (n=104) of non-smoking persons of the general population for the background levels of these haemoglobin adducts. The median values for HEVal, HPVal, CEVal, AAVal and GAVal in a group of 92 non-smoking persons were 18.1, 4.1, <0.5, 29.9 and 35.2 pmol/g globin, respectively. The adduct levels in 12 persons reporting exposure to passive smoke at home were similar for most adducts with median values of 17.2, 4.1, 1.0, 24.9 and 29.7 pmol/g globin for HEVal, HPVal, CEVal, AAVal and GAVal, respectively. Our results point to an elevated uptake of acrylonitrile caused by passive smoking as indicated by higher levels of the corresponding haemoglobin adduct CEVal.

  5. Studies on the physico-mechanical and thermal characteristics of blends of DGEBA epoxy, 3,4 epoxy cyclohexylmethyl, 3',4'-epoxycylohexane carboxylate and carboxyl terminated butadiene co-acrylonitrile (CTBN)

    Energy Technology Data Exchange (ETDEWEB)

    Tripathi, Garima [Department of Plastic Technology, H. B. Technological Institute, Kanpur 208002 (India); Srivastava, Deepak [Department of Plastic Technology, H. B. Technological Institute, Kanpur 208002 (India)], E-mail: deepak_sri92@rediffmail.com

    2008-11-25

    Toughening of blend of diglycidyl ether of bisphenol-A (DGEBA) and 3,4 epoxy cyclohexylmethyl, 3',4'-epoxycylohexane carboxylate, i.e. cycloaliphatic epoxy resin (CAE) with varying weight ratios (0-25 wt%) of carboxyl terminated butadiene acrylonitrile (CTBN) copolymer have been investigated. Fourier transform infrared (FTIR) spectroscopic analysis established that the interaction between oxirane groups of DGEBA, CAE and CTBN were responsible for characteristics peak shifts in the blends compared to their counterparts. Physico-mechanical properties of the prepared samples, e.g. tensile, flexural and impact strengths showed an optimum concentration of CTBN (15 wt%) into epoxy matrix, which offered maximum toughening. Thermal stability of the prepared samples was analyzed by dynamic thermogravimetric runs. Cross-sections of the cured samples which failed during impact testing have been critically studied through scanning electron microscopic (SEM) analysis to gain insight into the phase morphology.

  6. Study on Teratogenicity of Acrylonitrile in Rats by Subcutaneous Injection%皮下注射丙烯腈对大鼠致畸作用研究

    Institute of Scientific and Technical Information of China (English)

    崔金山; 杨衍凯; 付守林; 张玉敏; 段志文; 李海山; 王瀛; 张岸舸

    2001-01-01

    目的评价丙烯腈对雌性大鼠有无致畸作用。方法于雌性大鼠妊娠第7~16天皮下注射丙烯腈(AN)15,25,35 mg·kg-1,常规方法检测AN的胚胎毒性和致畸作用。结果 25 mg·kg-1组死胎率、吸收胎率升高,胎鼠平均体重、体长、尾长减小,与阴性对照组比较差异有显著性(P<0.05);35 mg·kg-1组除窝平均活胎数减少,差异有显著性( P<0.05),其余各指标与阴性对照组比较差异有非常显著性(P <0.01);25,35 mg·kg-1组畸胎率、母体畸胎率、活胎畸形率升高,与对照组相比差异有显著性和/或非常显著性(P<0.05或P <0.01),且有明确的剂量效应或剂量反应关系。本实验皮下注射AN染毒的致畸最低剂量为 15 mg·kg-1,致畸指数为6.3,以骨骼畸形为主,外观畸形主要为无尾、短尾等。结论丙烯腈皮下注射染毒有明显的胚胎毒性,致畸剂量小于经口染毒阈剂量,是一种弱致畸物。%Objective The teratogenicity of acrylonitrile(AN)on fe male rats was evaluated.Methods 15,25 and 35 mg/kg AN were administ ered by subcutaneous injection to rats on the time 7~16 d of gestation.Embryoto x icity and teratogenicity of AN were examined by a traditional teratogenic method .Results At the dosage of 25 mg/kg,AN could induce higher incidence of fetal resorption and death,and decrease the average fetal body weight and le ngth with significant difference(P<0.05)when compared with neg ative controls.At the dosage of 35 mg/kg,AN could decrease average vital fet us p er litter with significant difference(P<0.05),and induce chang es of other indexes with highly significant difference(P<0.0 1).At the dosage of 25 and 35 mg/kg,AN could induce higher teras rate,maternal t eras rate and malformation rate of vital fetus with significant and/or highly s ignificant difference(P<0.05 or P<0.01),resp ectively.There existed a dose-effect or dose-response relationship between abo ve

  7. GC Determination of Acetaldehyde, Acrolein and Acrylonitrile in Water with Purge and Trap Technique%吹扫捕集-气相色谱法测定水中乙醛、丙烯醛、丙烯腈

    Institute of Scientific and Technical Information of China (English)

    陆文娟; 王晋宇; 陈玲瑚; 赵辰

    2011-01-01

    Purge and trap technique was applied in the GC determination of acetaldehyde, acrolein and acrylonitrile in water. The analytes were purged, trapped and thermodesorbed using the Trap Vocarb 3000, and determined by CR2 with flame ionization detector (FID). Linear relationships between values of peak area and mass concentration of acetaldehyde, acrolein and acrylonitrile obtained were same in the range of 0. 020--0.20 mg·L^-1 , with detection limits (3S/N) of 0. 005, 0. 010, 0. 001mg·L^-1 respectively. Tests for recovery and precision were made by standard addition method, values of recovery found were in the range of 90. 0%-110.0% and values of RSD's (n=7) were less than 50%.%提出了吹扫捕集-气相色谱法测定水中乙醛、丙烯醛和丙烯腈的分析方法。样品用Trap Vocarb 3000捕集阱吹扫、捕集及热解析后,用气相色谱法氢火焰离子化检测器分析。3种化合物的质量浓度在0.020~0.20mg·L^-1的相同范围内与其峰面积呈线性关系,方法的检出限(3S/N)分别为0.005,0.010,0.001mg·L^-。标准加入回收率在90.0%~110.0%之间,相对标准偏差(n=7)均小于5%。

  8. Fast Determination of Acrolein and Acrylonitrile in Water by the Portable GC-MS and Selected Ion Monitoring%便携式GC-MS选择离子快速测定水中丙烯醛和丙烯腈

    Institute of Scientific and Technical Information of China (English)

    邓敏军; 罗艳; 黄小佳; 邓超冰; 梁柳玲; 杨安平

    2012-01-01

    Portable gas chromatography mass spectrometry (GC-MS) can simultaneously carry out qualitative and quantitative analysis of multi-component complex organic compounds and plays an increasingly important role in environmental monitoring, especially in the spot emergent monitoring. The Method of Fast Determination of Acrolein and Acrylonitrile in Water was established by the portable headspace gas chromatography and mass spectrometry (GC-MS) in this paper. It is suitable for environmental emergency monitoring and laboratory for analysis of acrolein and acrylonitrile in water because this method possessed relativity r >0. 997 , detection limits 5-10 μg/L and the average recoveries 93. 3% -99. 5% .%便携式气相色谱-质谱仪(GC-MS)能同时对多组分复杂有机物进行定性、定量分析,在环境监测尤其是事故现场应急监测中发挥越来越重要的作用.文章建立了便携式顶空-GC-MS选择离子测定水中丙烯醛、丙烯腈的分析方法,其相关性大于0.997,检测限为5~ 10μg/L,回收率为93.3%~99.5%,该方法适用于水中丙烯腈、丙烯醛的应急现场及日常实验室分析工作.

  9. Uterotrophic and Hershberber Assays for Acrylonitrile in Rats%丙烯腈类性激素作用的整体动物筛检试验

    Institute of Scientific and Technical Information of China (English)

    王宁; 荣顺兴; 朱菊一; 黄简抒; 周元陵; 金泰廙

    2005-01-01

    [目的]研究丙烯腈(AN)的类性激素样作用.[方法]①采用经典大鼠子宫增重方法测试丙烯腈的类雌激素样作用,对去卵巢SD大鼠皮下注射剂量分别为0、10、15、25、40、60 mg/kg受试物丙烯腈,每天一次、连续3天;同时皮下注射剂量为0.001 mg/kg雌二醇玉米油溶液为阳性对照组.最后一次给药24 h后,将大鼠麻醉后取血并处死,观察受试动物子宫湿重、干重、肝重、肾重等指标.②研究丙烯腈的抗雄激素作用.采用OECD推荐的内分泌干扰体内筛检实验方法(Hershberger试验),对雄性去势大鼠皮下注射剂量为0.4mg/kg体重丙酸睾酮,同时经口灌胃剂量分别为0,10,20,30,40,50 mg/kg体重的受试物丙烯腈以及25 mg/kg体重的阳性参照物氟他胺(flutamide,FLU),每天一次,连续10天.最后一次给药24 h后,将大鼠麻醉后取血并处死,观察受试动物前列腺、精囊腺、阴茎、肛提肌/球体海绵体肌、尿道球腺等附性腺组织(sex accessorytissue,SAT)重量和肝重、肾重等指标.[结果]①子宫增重实验:丙烯腈各剂量组大鼠子宫干重、湿重与溶剂对照组无显著差异(P>0.05),阳性对照组与溶剂对照组及丙烯腈各剂量组比较,子宫干重、湿重差异存在显著性(P<0.05).②Hershberger试验:丙烯腈各剂量组与阴性对照组相比,SAT重量差异无显著性(P>0.05),阳性对照组(FLU)与阴性对照组相比,SAT重量差别具有显著性(P<0.05).丙烯腈各剂量组肝、肾重量与阴性对照组差别无显著性(P>0.05),提示受试动物无明显系统毒性.[结论]采用子宫增重测试和Hershberger体内筛检试验未发现丙烯腈具有类性激素作用.%[ Objective ] To assess the estrogenic and anti-androgenic effects of acrylonitrile (AN) by in-vivo uterotrophic and Hershberger assays proposed by the OECD. [ Methods ] For the uterotrophic assay, AN was injected subcutaneously at the doses of 0, 10, 15, 25, 40 and 60mg/kg to

  10. 丙烯腈-苯乙烯磺酸共聚物/层状双金属氢氧化物纳米复合质子传导聚合物电解质的制备与表征%Synthesis and characterization of proton-conducting polymer electrolytes based on acrylonitrile-styrene sulfonic acid copolymer/layered double hydroxides nanocomposites

    Institute of Scientific and Technical Information of China (English)

    王盎然; 包永忠; 翁志学; 黄志明

    2008-01-01

    Acrylonitrile-sodium styrene sulfonate copolymer/layered double hydroxides nanocomposites were prepared by in situ aqueous precipitation copolymerization of acrylonitrile (AN) and sodium styrene sulfonate (SSS) in the presence of 4-vinylbenzene sulfonate intercalated layered double hydroxides (MgAl-VBS LDHs) and transferred to acrylonitrile-styrene sulfonic acid (AN-SSA) copolymer/LDHs nanocomposites as a proton-conducting polymer electrolyte. MgAl-VBS LDHs were prepared by a coprecipitation method, and the structure and composition of MgAl-VBS LDHs were determined by X-ray diffraction (XRD), infrared spectroscopy, and elemental analysis. X-ray diffraction result of AN-SSS copolymer/LDHs nanocomposites indicated that the LDHs layers were well dispersed in the AN-SSS copolymer matrix. All the AN-SSS copolymer/LDHs nanocomposites showed significant enhancement of the decomposition temperatures compared with the pristine AN-SSS copolymer, as identified by the thermogravimetric analysis. The methanol crossover was decreased and the proton conductivity was highly enhanced for the AN-SSA copolymer/LDHs nanocomposite electrolyte systems In the case of the nanocomposite electrolyte containing 2% (by mass) LDHs, the proton conductivity of 2.60×10-3 S·m-1 was achieved for the polymer electrolyte.

  11. Evaluation of the detoxication efficiencies for acrylonitrile wastewater treated by a combined anaerobic oxic-aerobic biological fluidized tank (A/O-ABFT) process: Acute toxicity and zebrafish embryo toxicity.

    Science.gov (United States)

    Na, Chunhong; Zhang, Ying; Deng, Minjie; Quan, Xie; Chen, Shuo; Zhang, Yaobin

    2016-07-01

    Acrylonitrile (ACN) wastewater generated during ACN production has been reported to be toxic to many aquatic organisms. However, few studies have evaluated toxicity removal of ACN wastewater during and after the treatment process. In this study, the detoxication ability of an ACN wastewater treatment plant (WWTP) was evaluated using Daphnia magna, Danio rerio and zebrafish embryo. This ACN WWTP has a combined anaerobic oxic-aerobic biological fluidized tank (A/O-ABFT) process upgraded from the traditional anaerobic oxic (A/O) process. Moreover, the potential toxicants of the ACN wastewaters were identified by gas chromatography-mass spectrometry (GC-MS). The raw ACN wastewater showed high acute and embryo toxicity. 3-Cyanopyridine, succinonitrile and a series of nitriles were detected as the toxic contributors of ACN wastewater. The A/O process was effective for the acute and embryo toxicity removal, as well as the organic toxicants. However, the A/O effluent still showed acute and embryo toxicity which was attributed by the undegraded and the newly generated toxicants during the A/O process. The residual acute and embryo toxicity as well as the organic toxicants in the A/O effluent were further reduced after going through the downstream ABFT process system. The final effluent displayed no significant acute and embryo toxicity, and less organic toxicants were detected in the final effluent. The upgrade of this ACN WWTP results in the improved removal efficiencies for acute and embryo toxicity, as well as the organic toxicants.

  12. Preparation and Characterization of Facilitated Transport Membranes Composed of Chitosan-Styrene and Chitosan-Acrylonitrile Copolymers Modified by Methylimidazolium Based Ionic Liquids for CO₂ Separation from CH₄ and N₂.

    Science.gov (United States)

    Otvagina, Ksenia V; Mochalova, Alla E; Sazanova, Tatyana S; Petukhov, Anton N; Moskvichev, Alexandr A; Vorotyntsev, Andrey V; Afonso, Carlos A M; Vorotyntsev, Ilya V

    2016-06-09

    CO₂ separation was found to be facilitated by transport membranes based on novel chitosan (CS)-poly(styrene) (PS) and chitosan (CS)-poly(acrylonitrile) (PAN) copolymer matrices doped with methylimidazolium based ionic liquids: [bmim][BF₄], [bmim][PF₆], and [bmim][Tf₂N] (IL). CS plays the role of biodegradable film former and selectivity promoter. Copolymers were prepared implementing the latest achievements in radical copolymerization with chosen monomers, which enabled the achievement of outstanding mechanical strength values for the CS-based membranes (75-104 MPa for CS-PAN and 69-75 MPa for CS-PS). Ionic liquid (IL) doping affected the surface and mechanical properties of the membranes as well as the gas separation properties. The highest CO₂ permeability 400 Barrers belongs to CS-b-PS/[bmim][BF₄]. The highest selectivity α (CO₂/N₂) = 15.5 was achieved for CS-b-PAN/[bmim][BF₄]. The operational temperature of the membranes is under 220 °C.

  13. Preparation and Characterization of Facilitated Transport Membranes Composed of Chitosan-Styrene and Chitosan-Acrylonitrile Copolymers Modified by Methylimidazolium Based Ionic Liquids for CO2 Separation from CH4 and N2

    Directory of Open Access Journals (Sweden)

    Ksenia V. Otvagina

    2016-06-01

    Full Text Available CO2 separation was found to be facilitated by transport membranes based on novel chitosan (CS–poly(styrene (PS and chitosan (CS–poly(acrylonitrile (PAN copolymer matrices doped with methylimidazolium based ionic liquids: [bmim][BF4], [bmim][PF6], and [bmim][Tf2N] (IL. CS plays the role of biodegradable film former and selectivity promoter. Copolymers were prepared implementing the latest achievements in radical copolymerization with chosen monomers, which enabled the achievement of outstanding mechanical strength values for the CS-based membranes (75–104 MPa for CS-PAN and 69–75 MPa for CS-PS. Ionic liquid (IL doping affected the surface and mechanical properties of the membranes as well as the gas separation properties. The highest CO2 permeability 400 Barrers belongs to CS-b-PS/[bmim][BF4]. The highest selectivity α (CO2/N2 = 15.5 was achieved for CS-b-PAN/[bmim][BF4]. The operational temperature of the membranes is under 220 °C.

  14. Morphology, mechanical, cross-linking, thermal, and tribological properties of nitrile and hydrogenated nitrile rubber/multi-walled carbon nanotubes composites prepared by melt compounding: The effect of acrylonitrile content and hydrogenation

    Energy Technology Data Exchange (ETDEWEB)

    Likozar, Blaz, E-mail: blaz.likozar@fkkt.uni-lj.si [Polymer Competence Center Leoben GmbH, Montanuniversitaet Leoben, Roseggerstrasse 12, A-8700 Leoben (Austria); Major, Zoltan, E-mail: zoltan.major@jku.at [Polymer Competence Center Leoben GmbH, Montanuniversitaet Leoben, Roseggerstrasse 12, A-8700 Leoben (Austria)

    2010-11-01

    The purpose of this work was to prepare nanocomposites by mixing multi-walled carbon nanotubes (MWCNT) with nitrile and hydrogenated nitrile elastomers (NBR and HNBR). Utilization of transmission electronic microscopy (TEM), scanning electron microscopy (SEM), and small- and wide-angle X-ray scattering techniques (SAXS and WAXS) for advanced morphology observation of conducting filler-reinforced nitrile and hydrogenated nitrile rubber composites is reported. Principal results were increases in hardness (maximally 97 Shore, type A), elastic modulus (maximally 981 MPa), tensile strength (maximally 27.7 MPa), elongation at break (maximally 216%), cross-link density (maximally 7.94 x 10{sup 28} m{sup -3}), density (maximally 1.16 g cm{sup -3}), and tear strength (11.2 kN m{sup -1}), which were clearly visible at particular acrylonitrile contents both for unhydrogenated and hydrogenated polymers due to enhanced distribution of carbon nanotubes (CNT) and their aggregated particles in the applied rubber matrix. Conclusion was that multi-walled carbon nanotubes improved the performance of nitrile and hydrogenated nitrile rubber nanocomposites prepared by melt compounding.

  15. Morphology, mechanical, cross-linking, thermal, and tribological properties of nitrile and hydrogenated nitrile rubber/multi-walled carbon nanotubes composites prepared by melt compounding: The effect of acrylonitrile content and hydrogenation

    Science.gov (United States)

    Likozar, Blaž; Major, Zoltan

    2010-11-01

    The purpose of this work was to prepare nanocomposites by mixing multi-walled carbon nanotubes (MWCNT) with nitrile and hydrogenated nitrile elastomers (NBR and HNBR). Utilization of transmission electronic microscopy (TEM), scanning electron microscopy (SEM), and small- and wide-angle X-ray scattering techniques (SAXS and WAXS) for advanced morphology observation of conducting filler-reinforced nitrile and hydrogenated nitrile rubber composites is reported. Principal results were increases in hardness (maximally 97 Shore, type A), elastic modulus (maximally 981 MPa), tensile strength (maximally 27.7 MPa), elongation at break (maximally 216%), cross-link density (maximally 7.94 × 1028 m-3), density (maximally 1.16 g cm-3), and tear strength (11.2 kN m-1), which were clearly visible at particular acrylonitrile contents both for unhydrogenated and hydrogenated polymers due to enhanced distribution of carbon nanotubes (CNT) and their aggregated particles in the applied rubber matrix. Conclusion was that multi-walled carbon nanotubes improved the performance of nitrile and hydrogenated nitrile rubber nanocomposites prepared by melt compounding.

  16. The effect of graphene oxide on the polymerization of acrylonitrile and its rheological properties%氧化石墨烯对丙烯腈聚合及溶液流变性能的影响

    Institute of Scientific and Technical Information of China (English)

    巩娜娟; 吕永根; 杨常玲; 陆叶涛

    2013-01-01

    Graphene oxide modified polyacrylonitrile (GO/PAN) was prepared by in situ polymerization. The effects of the GO on the polymeration of acrylonitrile and the rheological properties of PAN solution were studied. The results showed that GO slightly hindered the polymerization, and the molecular weight and conversion rate of GO/PAN solution decreased with the increasing content of GO. GO facilitated the fluidity of PAN solution. All the storage modulus, loss modulus and viscosity of the GO/PAN solution decreased with the increasing content of GO, and the GO/PAN solution is prone to be viscous with increasing content of GO.%采用原位聚合法制备了氧化石墨烯/聚丙烯腈(GO/PAN)共聚物,研究了GO对丙烯腈聚合及PAN纺丝溶液流变性能的影响.结果表明,GO对聚合反应有一定的抑制作用,GO/PAN的相对分子质量和转化率均随着GO质量分数的增加而减小;GO的加入增加了PAN的流动性,GO/PAN溶液的储能模量、损耗模量和粘度均随着GO质量分数的增加而减小,并且随着GO质量分数的增加更倾向于粘性.

  17. Poly(methyl methacrylate-acrylonitrile-ethyl acrylate) terpolymer based gel electrolyte for LiNi0.5Mn1.5O4 cathode of high voltage lithium ion battery

    Science.gov (United States)

    Sun, Ping; Liao, Youhao; Xie, Huili; Chen, Tingting; Rao, Mumin; Li, Weishan

    2014-12-01

    A novel gel polymer electrolyte (GPE), based on poly(methyl methacrylate-acrylonitrile-ethyl acrylate) (P(MMA-AN-EA)) terpolymer, is designed to match LiNi0.5Mn1.5O4 cathode of 5 V lithium ion battery. The performances of the synthesized P(MMA-AN-EA) terpolymer and the corresponding membrane and GPE are investigated by scanning electron microscope, energy dispersive spectroscopy, nuclear magnetic resonance spectra, Fourier transform infrared spectra, thermogravimetric analyzer, electrochemical impedance spectroscopy, linear sweep voltammetry, and charge/discharge test. It is found that the pore structure of P(MMA-AN-EA) membrane is affected by the dose of pore forming agent, polyethylene glycol (PEG400). The membrane with 3 wt% PEG400 presents the best pore structure, in which pores are dispersed uniformly and interconnected, and exhibits the largest electrolyte uptake, resulting in the highest ionic conductivity of 3.82 × 10-3 S cm-1 for the corresponding GPE at room temperature. The GPE has improved compatibility with lithium anode and is electrochemically stable up to 5.2 V (vs. Li/Li+). The high voltage LiNi0.5Mn1.5O4 cathode using the resulting GPE exhibits excellent cyclic stability, maintaining 97.9% of its initial discharge capacity after 100 cycles compared to that of 79.7% for the liquid electrolyte at 0.5 C.

  18. Inlfuence of Different Toughness Agents on Weatherability of Acrylonitrile-Styrene Copolymer%不同增韧剂对丙烯腈-苯乙烯共聚物耐候性的影响

    Institute of Scientific and Technical Information of China (English)

    贺芳; 黄兴宇; 钱晶; 申娟

    2015-01-01

    Using seven different toughness agents in acrylonitrile-styrene copolymer(SAN Resin)was studied,the influence of high glue powder,acrylic resin(ACR),maleic anhydride grafted EPDM (EPDM–g–MAH),styrene copolymer(MBS),ethylene butyl acrylate(EBA),maleic anhydride grafted PE–LD(PE–LD–g–MAH)and ethylene methyl acrylate(EMA) on mechanical properties of acrylonitrile styrene copolymer(SAN resin)was respectively researched. And temperature test machine and xenon lamp climate chamber were used to analysis of the influence of different toughness agents on the weatherability of SAN. The results show that compared with other toughness agents,the impact strength of SAN resin with MBS is the best. The impact strength of SAN resin is decreasing with the lower temperature,EBA and EPDM–g–MAH could improve the impact strength of SAN resin in low temperature. And Xenon lamp aging test results show that the SAN resin will appear the phenomenon of xanthochroia after xenon lamp aging test,but EPDM–g–MAH,MBS and EBA could improve the light resistance properties of SAN resin,and the effect of EPDM–g–MAH is the best.%采用7种增韧剂:高胶粉、丙烯酸酯类树脂(ACR),马来酸酐接枝三元乙丙橡胶(EPDM–g–MAH),苯乙烯三元共聚物(MBS),乙烯丙烯酸丁酯(EBA),马来酸酐接枝低密度聚乙烯(PE–LD–g–MAH),乙烯–甲基丙烯酸酯(EMA)对丙烯腈-苯乙烯共聚物(SAN)进行增韧改性,通过高低温实验箱和氙灯人工气候试验箱来研究各增韧剂对SAN耐候性的影响。结果表明,添加增韧剂MBS的SAN冲击强度最高;随着温度的降低,SAN的冲击强度是下降的, EBA,EPDM–g–MAH能改善SAN的低温冲击强度;氙灯光照老化试验结果表明,SAN经过光照老化后都会出现黄变现象,而添加了EPDM–g–MAH,MBS,EBA的SAN的耐光照老化性能都有所提高,其中添加了EPDM–g–MAH的耐光照老化性最好。

  19. Performance improvement of gel- and solid-state dye-sensitized solar cells by utilization the blending effect of poly (vinylidene fluoride-co-hexafluropropylene) and poly (acrylonitrile-co-vinyl acetate) co-polymers

    Science.gov (United States)

    Venkatesan, Shanmugam; Obadja, Nesia; Chang, Ting-Wei; Chen, Li-Tung; Lee, Yuh-Lang

    2014-12-01

    Poly (vinylidene fluoride-co-hexafluropropylene) (PVDF-HFP) and poly (acrylonitrile-co-vinyl acetate) (PAN-VA) are used as gelator to prepare gel- and solid-state polymer electrolytes for dye sensitized solar cells (DSSCs) applications. The electrolytes prepared using PVDF-HFP have higher conductivities than those prepared using PAN-VA. In blended polymers, the conductivities of the electrolytes increase with increasing composition of PVDF-HFP; at 75% PVDF-HFP, conductivity of the blended polymer surpassed that of pure polymers. It is also found that the viscosity of the electrolyte prepared by PAN-VA (1.2 kPaS) is much lower than that by PVDF-HFP (11 kPaS). Therefore, increasing PAN-VA composition can decrease the viscosity of the electrolyte, improving the penetration of electrolytes in the TiO2 matrix. By controlling the ratio of PVDF-HFP/PAN-VA, the conductivity and viscosity of the electrolyte can be regulated and an optimal ratio based on the conversion efficiency of the gel- and solid state DSSCs is obtained at the ratio of 3/1. The highest efficiency achieved by the gel- and solid-state cells using the blending polymers are 6.3% and 4.88%, respectively, which are higher than those prepared using pure polymers (5.53% and 4.56%, respectively). The introduction of TiO2 fillers to the solid electrolyte can further increase the cell efficiency to 5.34%.

  20. 丙烯腈-三元乙丙橡胶-苯乙烯接枝共聚物AES的表征%Characterization of graft copolymer of styrene and acrylonitrile onto EPDM (AES)

    Institute of Scientific and Technical Information of China (English)

    董颖; 王辉; 金春玉; 赵彦广; 裴洪; 温冬梅; 刘洪伟; 邹向阳

    2012-01-01

    采用苯乙烯和丙烯腈接枝三元乙丙橡胶合成丙烯腈-三元乙丙橡胶-苯乙烯接枝共聚物AES,用其和苯乙烯-丙烯腈(SAN)树脂共混得到AES树脂.对合成的AES树脂样品进行常温相对分子质量及相对分子质量分布的测定,红外光谱、热稳定性与微观结构表征,并与目标样品进行对比.得出三元乙丙橡胶已接枝上SAN支链,即三元乙丙橡胶与苯乙烯及丙烯腈发生了接枝共聚合反应;合成样品相对分子质量及相对分子质量分布数据、热稳定性数据及微观结构与目标样品接近;合成样品AES粉料和SAN树脂基本均匀混合的结论.%In this paper, the graft copolymer of styrene and acrylonitrile onto EPDM(AES) was prepared and blended with SAN resin, the synthesized AES was characterized by infrared spectrum. Relative molecular weight and its distribution, heat stability, and microcosmic structure of the AES were determined and compared with the target AES. Results showed that the graft copolymerization of AES has happended,the properties of AES are near to that of the target AES.

  1. 腈纶皂化制备电流变液悬浮粒子的研究%Studies on Saponification of Acrylonitrile Terpolymer for Suspending Particles of Electrorheological Fluids

    Institute of Scientific and Technical Information of China (English)

    吴孟强; 陈艾

    2001-01-01

    In order to prepare suspending particles for electrorheological fluids, hetergeneous hydrolysis of acrylonitrile terpolymer is conducted in presence of saponifying agent(sodium hydroxide) in this paper. The effects of the saponification conditions such as the amount of added sodium hydroxide, time duration and temperature on the degree of saponification are studied in detail. Meanwhile, the conversion of nitrile groups is discussed with the result that the saponification of nitrile groups of the terpolymer initially yields amide groups, then slows down to carboxylic groups. The research sets a way for the preparation of dispersing particles of water-free electrorheological fluids tentatively used for controlling light transmittance.%为了制备无水电流变液用悬浮粒子,研究了腈纶在碱性条件下的多相水解。详细考察了皂化试剂氢氧化钾的用量,皂化时间和温度等皂化条件对皂化程度的影响; 讨论了氰基转化过程。研究结果表明,在皂化初期,腈纶分子链上的氰基转化为酰胺基,然后缓慢转化为羧基。给出了一条制备无水电流变液用悬浮粒子的方法,并初步考察了该类电流变液的控光特性。

  2. 淀粉丙烯腈接枝共聚物皂化制备吸水剂%The Preparation Technology of Water-Absorbent by the Saponification of the Graft Copolymer of Starch and Acrylonitrile

    Institute of Scientific and Technical Information of China (English)

    顾正彪; 吴嘉根

    2001-01-01

    通过对淀粉丙烯腈接枝共聚物(SPAN)皂化制备吸水剂HSPAN的研究表明:HSPAN为水不溶性凝胶,但具有很强的吸水能力.以氢氧化钾皂化,酸作沉淀剂,经洗涤、分散和干燥制备HSPAN的工艺路线较为理想.皂化工艺条件在用碱量为SPAN中接枝链部分摩尔数的1.1倍、皂化温度95°C以上、皂化时间大于3h,且HSPAN的平板干燥温度在70°C时最好.当SPAN接枝百分率在70%左右时,制得的HSPAN吸水率最高.%Studies on the Preparation Technology of Water-absorbent (HSPAN)by the Saponification of the graft Copolymer of Starch and Acrylonitrile (SPAN) showed that, HSPAN was a kind of gel which was insoluble in water but could absorb a great amount of water. The best technology for the preparation of HSPAN was that,after SPAN was saponified by potassium hydroxide, precipited by sulfuric acid, washed and dispersed in water again, HSPAN was obtained by drying it on a plate. Moreover, the best conditions were that,the quantity of potassium hydroxide used in saponification was 1.1 as much as the mole of polyacrylonitrile in SPAN, saponifying temperature over 95°C, reaction time more than 3 h and drying temperature at 70°C. In addition, the highest water-absorbing capacity could be obtained from the SPAN in which grafted ratio was 70% or so.

  3. 高负荷下臭氧催化氧化深度处理丙烯腈废水运行特性%Operation characteristics of catalytic ozonation under the high load condition for the treatment of acrylonitrile wastewater

    Institute of Scientific and Technical Information of China (English)

    陈中英

    2015-01-01

    采用臭氧催化氧化技术对大庆炼化公司丙烯腈废水进行深度处理,处理能力为20 m3/h。在实际进水COD远远高于设计进水浓度条件下,臭氧催化氧化装置对COD的去除总量大大高于设计值(1 kg/h),平均为1.88 kg/h。在高负荷条件下,该装置处理效果优于预期,但同时也存在催化剂污染等问题。通过每周1次的定期气水联合反洗,可保证装置稳定运行并维持良好的处理效果。%Catalytic ozo nation technology has been used for the advanced treatment of the acrylonitrile wastewater from Daqing Branch,Oil Refinery Chemical Co.,CNPC,whose treatment capacity is 20 m3/h. Under the condition that the COD of actual influent is much higher than the designed influent concentration ,the total amount of COD removing capacity is averagely 1.88 kg/h,much higher than the initially designed value,1 kg/h. Under the high load condition,the treatment effect of this system is better than what was expected,but in the meanwhile,problems,such as catalyst pollution,etc.,have occurred. By means of periodic air-water backwashing once a week,the system can run steadily and keep good treatment effect.

  4. Effect of heat treatment on the mechanical properties of Casein-g-Poly(acrylonitrile) fibers%热处理对酪蛋白改性丙烯腈纤维力学性能的影响

    Institute of Scientific and Technical Information of China (English)

    高晶; 俞建勇; 任海龙

    2009-01-01

    对4种不同投料比酪蛋白接枝丙烯腈纤维的不同热处理条件下机械性能进行了研究.结果显示,酪蛋白接枝改性丙烯进纤维的性能随温度变化比较敏感,且酪蛋白投料比含量越大,高温处理对纤维交互作用的影响越显著,纤维的断裂强度和断裂伸长均有所提高.但高温处理后酪蛋白纤维由于热氧化分解而使其颜色逐渐发黄.纤维的横截面SEM图像显示了不同投料比改性纤维的内部结构.%Four kinds of casein-g-poly (acrylonitrile) fibers with different casein content were prepared, and mechanical properties were investigated after different heat treatment. The results show that the grafted casein fibers were sensitive to temperature. With the increase of casein content, the effect of cross-linking performance in fiber increased after high temperature treatment. The strength and elongation at break both trended to increase. But the colors of fibers gradually changed into yellow under the higher temperature, due to the thermal oxidative decomposition of casein. SEM observations on the cross-section surface of modified fibers show the different structures in grafted casein fibers with different casein contents.

  5. NMR measurement of identical polymer samples by round robin method. 4. Analysis of composition and monomer sequence distribution in poly(methyl methacrylate-co-acrylonitrile) leading to determinations of monomer reactivity ratios

    Energy Technology Data Exchange (ETDEWEB)

    Hatada, Koichi; Kitayama, Tatsuki; Terawaki, Yoshio [Osaka Univ., Toyonaka (Japan). Faculty of Engineering Science] [and others

    1995-11-01

    In order to assess the reliability of NMR measurement of polymers, {sup 1}H and {sup 13}C NMR data for three copolymers of methyl methacrylate (MMA) and acrylonitrile (AN) prepared with AIBN were collected from 46 spectrometers whose resonance frequencies for {sup 1}H NMR measurements ranging from 90 to 500 MHz. {sup 1}H and {sup 13}C NMR spectra were measured in nitrobenzene-d{sub 5} at 110degC and acetonitrile-d{sub 3} at 70degC, respectively. Standard deviations ({sigma}`s) for chemical shift measurements of the {sup 1}H and {sup 13}C NMR signals were 0.003-0.008 ppm and 0.03-0.05 ppm, respectively. Compositions of the copolymers were determined from the relative intensities of the signals due to the OCH{sub 3} (MMA) and CH (AN) protons, and the {sigma} values for the determinations were 3.7-9.5%. The compositions determined from {sup 13}C NMR (C = O for MMA unit, CN for AN unit) agreed well with those obtained from {sup 1}H NMR. Monomer reactivity ratios r{sub ij} (i,j = 1 or 2) for a penultimate model were determined from monomer feed ratios and triad fractions obtained from the C = O (MMA) and CH (AN) carbon signals. Most of the {sigma} values for r{sub ij} determinations were 5-14%. While r{sub 22} and r{sub 12} are nearly equivalent, r{sub 11} and r{sub 21} are significantly different from each other, indicating a possible existence of the penultimate-unit effect in the copolymerization of MMA and AN. Terminal model reactivity ratios, r{sub 1} and r{sub 2}, determined formally from the compositions of three samples by Fineman-Ross method showed large {sigma} values (22-24%). (author).

  6. Stability improvement of gel-state dye-sensitized solar cells by utilization the co-solvent effect of propionitrile/acetonitrile and 3-methoxypropionitrile/acetonitrile with poly(acrylonitrile-co-vinyl acetate)

    Science.gov (United States)

    Venkatesan, Shanmugam; Su, Song-Chuan; Kao, Shon-Chen; Teng, Hsisheng; Lee, Yuh-Lang

    2015-01-01

    Propionitrile (PPN) or 3-methoxypropionitrile (MPN) is mixed with acetonitrile (ACN) to prepare ACN/PPN and ACN/MPN co-solvents and used to fabricate polymer gel electrolytes (PGEs) of dye-sensitized solar cells (DSSCs), aiming at improving the stability of gel-state DSSCs. Co-solvents with various ratios are utilized to prepare PGEs using poly(acrylonitrile-co-vinyl acetate) (PAN-VA) as the gelator. The ratio effects of the co-solvents on the properties of PGEs and the performances of the corresponding DSSCs are studied. The results show that in-situ gelation of the gel-electrolytes can still be performed at the presence of 40% PPN or 30% MPN. However, increasing the composition of PPN and MPN in the co-solvents triggers a decrease in the diffusivity and conductivity of the PGEs, but an increase in the viscosity. Therefore, the energy conversion efficiencies of the cells decrease as a result. However, the introduction of PPN and MPN elevates the gel-to-liquid transition temperature (Tp) of the PGEs which significantly increases the stability of the gel-state DSSCs. Comparing between the effects of the two co-solvents, PPN and MPN have similar effect on elevation of Tp, but the conductivity of PGEs and the corresponding cell efficiency are higher for the ACN/PPN system, attributed to its lower viscosity compared with ACN/MPN system. By using the ACN/PPN (60/40) co-solvent at the presence of TiO2 fillers, gel-state cell with an efficiency of 8.3% can be achieved, which is even higher than that obtained by the liquid state cell (8%). After 500 h test at 60 °C, the cell can retain 95.4% of its initial efficiency.

  7. Synthesis of (Z)-2-Methyl-2-Butenedioic Acid-l-Methyl Ester and Determination of Apparent Reactivity Ratio of Copolymerization with Acrylonitrile%2-甲基-2-丁烯二酸单甲酯的合成及其与丙烯腈二元共聚的表观竞聚率的测定

    Institute of Scientific and Technical Information of China (English)

    杨俊锋; 陆国林; 谭久青; 黄晓宇; 陈惠芳; 潘鼎

    2008-01-01

    以柠糠酸酐为原料,合成了一种可以与丙烯(AN,acrylonitrile)共的新单体:2-甲基-2-丁烯二酸单甲酯(MBAME).以偶氮二异丁腈(AIBN,2,2'-azobis isobutyronitrle)为引发剂,70℃下引发MBAME与AN在N,N-二甲基甲酰胺(DMF,N,N-dimethylformamide)中进行无规共聚,通过Fineman-Ross法测定了两者在DMF溶液聚合体系的表观竞聚率,γ1(AN)=7.985,γ2(MBAME)=0.599,有助于优化聚丙烯腈基碳纤维用树脂的生产工艺.

  8. Mechanism of Graft Polymerization of Methyl Methacrylate-Acrylonitrile onto Poly (ethene-co-1-butene)%PEB/MMA-AN悬浮接枝共聚反应机理

    Institute of Scientific and Technical Information of China (English)

    熊凯; 朱勇平; 王霞; 王炼石; 蔡彤曼; 张安强; 曾祥斌

    2012-01-01

    研究了乙烯-1-丁烯共聚物(PEB)弹性体与甲基丙烯酸甲酯(MMA)-丙烯腈(AN)悬浮接枝共聚反应行为及接枝共聚产物对SAN树脂增韧作用随反应时间的变化规律,用凝胶渗透色谱法和傅里叶变换红外光谱法对接枝共聚产物进行了表征,分析了接枝共聚反应机理,推算了接枝链分子量.结果表明,体系首先发生链增长自由基向PEB转移终止形成非接枝共聚物(MANL)和PEB大分子自由基引发单体共聚形成接枝链(g-MAN)的反应,接枝反应结束后体系发生明显的非接枝共聚形成非接枝共聚物(MANH)的反应;MANL的分子量低于g-MAN的分子量,而g-MAN的分子量明显低于MANH的分子量;在接枝共聚过程中发生已接枝和未接枝PEB断链并随机再接生成多嵌段共聚物的副反应;在反应初期,接枝链的AN单元含量接近于非接枝共聚物的AN单元含量,在反应中后期前者远低于后者.%The effects of reaction time on reaction behavior of suspension grafting copolymerization of methyl methacrylate(MMA)-acrylonitrile( AN) onto poly(ethene-co-l-butene) (PEB) and toughening effect of PEB-g-MAN on SAN resin were investigated. The grafting polymerization product was characterized by GPC and FTTR analysis, the grafting copolymerization mechanism was investigated and the formula of calculating molecular weight of grafted chain was established. The results show that firstly the polymerization is mainly forming non-grafted copolymer with low molecular weight( MANL) of the transferring terminating polymerization of chain propagating free radicals and forming the grafted chains(g-MAN) of the transferring graft polymerization, and then the polymerization is mainly forming non-grafted copolymer with high molecular weight( MANH) of bimolecular terminating polymerization of chain propagating free radicals; molecular weight of MANL is less than that of g-M AN and molecular weight of g-M AN is less than that of MANH; there

  9. Study on Sulfomethylation of Cellulose Copolymer Copolymerized with Acrylonitrile and Acrylamide%纤维素-丙烯腈-丙烯酰胺共聚物磺甲基化改性研究

    Institute of Scientific and Technical Information of China (English)

    黄统琳; 刘明华; 刘剑锋; 詹怀宇

    2011-01-01

    The nitrile spherical cellulose adsorbent (SCAN) was prepared by sulfomethylating the prepared copolymer of grafting acrylonitrile and acrylamide onto the spherical cellulose beads, doing so is in order to provide reference data for getting higher application value of cellulose. The spherical cellulose beads were prepared by NMMO (N-methylmorpholine-N-oxide) process and sequential cooling technique. The sulfomethylation process was optimized through the orthogonal experiments and single-factor experiments. The results indicate that the adsorbent prepared has a specific surface area of 207.9 m2g-1, and sulfonation degree of 56.32% can be obtained under following optimal operating conditions: the solution pH=12, the mass ratio of HCHO, NaHSO3 and copolymer is 4:6:10, the reaction temperature is 50℃ and the reaction time is 5 h. In addition, the effect of sulfonation degree on the adsorption capacity of SCAN was also studied by using berberine hydrochloride as adsorbate. The results indicate that the increase of sulfonation degree is beneficial to the adsorption capacity, the maximum adsorption capacity of SCAN could reach 16.64 mg-g-1.%研制和开发新型改性纤维素类吸附剂,将是吸附剂研究的一个焦点.研究在球形纤维素珠体接枝丙烯腈和丙烯酰胺的基础上对其进行磺甲基化改性,制备出一种含腈基球形纤维素吸附剂(SCAN),以期为纤维素高值化利用提供参考数据.球形纤维素珠体由NMMO法和程序降温法制备.并通过正交试验和单因素实验进行工艺优化.实验结果表明,SCAN具有较大比表面积—207.9 m2·g-1,且在溶液pH=12,m(HCHO)∶m(NaHSO3)∶m(copolymer)=4∶6∶10,反应温度50℃下反应5h时的磺化度最高,为56.32%,以盐酸小檗碱为吸附质,研究磺化度对吸附剂吸附效果的影响,结果表明,在实验研究的磺化度范围内,磺化度越高,吸附效果越好,最大吸附量达16.64 mg·g-1.

  10. Synthesis and Properties of Melt Processable Acrylonitrile-N-vinylimidazole Copolymers and Fiber†%可熔融丙烯腈-N-乙烯基咪唑共聚物及纤维的制备与性能

    Institute of Scientific and Technical Information of China (English)

    韩娜; 李慧慧; 李传宝; 张兴祥; 李伟; 王栋

    2015-01-01

    采用自由基溶液聚合法制备了不同投料摩尔比的丙烯腈( AN)-N-乙烯基咪唑( VIM)共聚物[P(AN-co-VIM)].将 n(AN): n(VIM)为82:18和80:20的 P(AN-co-VIM)共聚物于210~220℃熔融纺丝制备了P(AN-co-VIM)初生纤维.通过傅里叶变换红外光谱、核磁共振(1 H NMR)谱、差示扫描量热分析、X 射线衍射分析和热台显微镜对 P(AN-co-VIM)共聚物的组成、热力学和结晶行为进行了表征.结果表明,自由基溶液聚合法可成功制备 P(AN-co-VIM)共聚物,当 VIM 的摩尔分数大于10%时,共聚物具有可熔融加工性.随着 VIM 摩尔分数的增加,共聚物的熔点降低,当 VIM 含量为20%时,共聚物的熔点从317℃降低至180℃,其分解温度最高为313.7℃.扫描电子显微镜(SEM)和电子单纤维强力测试.结果表明,纤维的表面光滑,断面结构致密,初生纤维的断裂强度为1.58 cN/ dtex,断裂伸长率为11.2%,有望广泛应用于碳纤维领域.%Polyacrylonitrile(PAN) and acrylonitrile(AN)-N-vinylimidazole(VIM) copolymers[ abbreviated as P(AN-co-VIM)] with various n(AN) : n(VIM)(93 : 7—80 : 20) were synthesized by free-radical solution copolymerization in dimethyl formamide ( DMF). The P ( AN-co-VIM) copolymers (82 : 18 and 80 : 20) possessed good melt processability, which were melt spun at the temperature of 210—220 ℃. The crystallinity, thermodynamics behavior and the composition of P(AN-co-VIM) copolymers were studied and characterized by ubbelodhe viscosimeter, Fourier transform infrared spectroscopy( FTIR), nuclear magnetic resonance ( 1 H NMR), differential scanning calorimetry( DSC), X-ray diffraction( XRD) analyses and hot stage microscope. The results revealed that P(AN-co-VIM) could be synthesized successfully by free-radical solution copolymerization. P( AN-co-VIM) could be melt processable as VIM molar fraction is higher than 10% . The melting temperature of P ( AN-co-VIM) shifts continuously to the lower temperature with the

  11. 29 CFR 1910.1045 - Acrylonitrile.

    Science.gov (United States)

    2010-07-01

    ...), strong bases, copper, copper alloys, ammonia, and amines. C. Sources of ignition such as smoking and open..., ammonia, and amines may start serious decomposition. 3. Hazardous decompostion products: Toxic gases and... monomer; synthesis of acrylic fibers, ABS, SAN, and nitrile barrier plastics and resins, nitrile...

  12. Fast Determination of Acrylonitrile, Crotonaldehyde, Pyridine and Quinoline in Environmental Tobacco Smoke with APCI-MS/MS%APCI-MS/MS法快速测定环境烟气中的丙烯腈、巴豆醛、吡啶和喹啉

    Institute of Scientific and Technical Information of China (English)

    蒋成勇; 王慧; 孙世豪; 宗永立; 王宏伟; 张建勋; 李炎强

    2013-01-01

    In order to determine the chemical pollutants in environmental tobacco smoke (ETS) which might possess potential risks to human health and environment, an atmospheric pressure chemical ionization (APCI)-tandem mass spectrometry (MS/MS) method was established to fast analyze four volatile and semi-volatile organic compounds (acrylonitrile, crotonaldehyde, pyridine and quinoline) in ETS. The ETS samples without any pretreatment was directed into a modified APCI ion source via inlet end of mass spectrometer and analyzed under multi-reaction monitoring (MRM) mode. The results showed that the calibration curves of the four compounds exhibited good linear relations (R2>0.999) with the limits of detection from 0.39 to 0.70 ng/L and the relative standard deviations (RSDs) from 5.14% to 9.42%. This method is simple in operation and features higher sensitivity, it is suitable for the fast analysis of acrylonitrile, crotonaldehyde, pyridine, and quinoline in ETS.%为了测定环境烟气(ETS)中对人体和环境有潜在危害的化学污染物,建立了一种快速分析丙烯腈、巴豆醛、吡啶和喹啉4种挥发性、半挥发性有机化合物的大气压化学电离(APCI)-串联质谱(MS/MS)方法.采集的ETS样品不经任何前处理,由质谱进样端直接引入到改造后的APCI离子源内,采用多反应监测模式(MRM)对其进行快速定量分析.结果表明:4种有机化合物的定量分析标准工作曲线线性关系较好(R2>0.999),检测限和相对标准偏差分别为0.39 ~ 0.70 ng/L和5.14% ~ 9.42%.该方法操作简单、灵敏度高,适合于快速检测ETS中的丙烯腈、巴豆醛、吡啶和喹啉.

  13. 丙烯腈生产中吸收塔尾气焚烧炉烟气余热的回收利用%Recovery and utilization of waste heat in flue gas from absorber off gas incinerator in acrylonitrile production

    Institute of Scientific and Technical Information of China (English)

    刘进阳; 卢苇; 刘纪云; 徐昆; 陈汉; 许浩

    2016-01-01

    结合某200 kt丙烯腈生产项目设计氨水吸收式梯级制冷系统,用以回收丙烯腈项目排出的吸收塔尾气焚烧炉(AOGI)烟气余热。通过该系统既可制取-10℃的盐水,替代此项目原有螺杆乙二醇制冷机达到丙烯腈单元的生产要求;又可制取-5℃的冰,可以应用于餐饮行业保存食物等。应用MATLAB软件对设计系统进行仿真,并采用夹点技术进行分析计算。实验结果表明,系统共回收AOGI烟气量1.67×105 Nm3/h,可制取621 kW的冷量,共节约电量187.11 kW,一年可节省人民币约95万元。%A multiple ammonia-water absorption refrigeration system was designed to recover and utilize waste heat in flue gas from Absorber Off Gas Incinerator(AOGI) in a 200 kt acrylonitrile production unit. The designed system could get-10℃ inorganic salt water solution to replace the former screw glycol refrigerating machine in the unit. It could meet the production requirement for the acrylonitrile unit and the system could product-5℃ ice at the same time And the ice may be applied in food industry to preserve food,etc. The designed system was simulated by means of the MATLAB software and was calculated by pinch technology. It could be concluded that this system could recover the AOGI flue gas volume of 1.67×105 Nm3/h,gain the cooling capacity of 621 kW,save electric power of 187.11 kW and economize about¥950,000 per year.

  14. Effects of milk and coenzyme Q10 on the interference of acrylonitrile on vascular endothelial functions%牛奶和辅酶Q10对丙烯腈致血管内皮功能紊乱的影响

    Institute of Scientific and Technical Information of China (English)

    郭进; 王卫群; 龚辉

    2011-01-01

    目的 探讨牛奶或辅酶Q10预处理对丙烯腈致大鼠血管内皮功能紊乱的影响.方法 将80只大鼠分为4组:对照组、单纯丙烯腈组、牛奶组、辅酶Q10组.采用灌胃染毒法,对照组仅予玉米油(丙烯腈的溶剂,1 ml/100 g),其他3组予丙烯腈25 mg/kg染毒.牛奶组和辅酶Q10组在染毒前30 min分别给予牛奶、辅酶Q10预处理.染毒12周后检测血清及主动脉组织中诱导型一氧化氮合酶(iNOS)和内皮型一氧化氮合酶(eNOS)的活力.结果 单纯丙烯腈组、牛奶组、辅酶Q10组血清iNOS水平[(42.9±2.5)U/ml、(26.5±4.4)U/ml、(26.7±3.3)U/ml]比对照组[(21.9±1.6)U/ml,P<0.05]升高.主动脉组织中iNOS在单纯丙烯腈组、牛奶组、辅酶Q10组[(0.812±0.008)、(0.773±0.019)、(0.622±0.013)U/mg蛋白]比对照组[(0.540±0.028)U/mg蛋白,P<0.05]高;而辅酶Q10组的主动脉eNOS活力[(0.471±0.011)U/mg蛋白]高于对照组、单纯丙烯腈组和牛奶组[(0.371±0.029)、(0.380±0.016)、(0.425±0.020)U/mg蛋白,P<0.05].结论 牛奶和辅酶Ql0可以缓解丙烯腈致血管内皮功能紊乱作用.%Objective To explore the influences of milk or coenzyme Q10 pretreatment to acrylonitrile on vascular endothelial functions in rats.Methods A total of 80 rats were randomly divided into 4 groups:control group(Con),acrylonitrile exposure group(ACN),milk pretreatment group (M + ACN)and coenzyme Q10 pretreatment group(Q10 + ACN).The experiment was conducted by the method of gavage exposure in rats.Control group was exposed to corn oil;acrylonitrile was administered to other three groups at the doses of 25 mg/kg.The M + ACN and Q10 + ACN groups were pretreated by milk or coenzyme Q10 at 30 minutes before acrylonitrile exposureAfter a 12-week exposure,the activities of inducible nitric oxide synthase(iNOS)and endothelial nitric oxide synthase(eNOS)were measured in serum and aortal tissues.Results As compared with Con group[(21.9 ± 1.6)U/ml],the activity of blood serum i

  15. Preparation, characterization and properties of butyl acrylate-styrene- acrylonitrile copolymer/titanium dioxide composite film%丙烯酸丁酯-苯乙烯-丙烯腈共聚物/二氧化钛复合薄膜的制备、表征及性能

    Institute of Scientific and Technical Information of China (English)

    徐慧; 史铁钧; 孙建新; 杨兆攀

    2011-01-01

    先以丙烯酸丁酯、苯乙烯和丙烯腈为原料,通过种子乳液聚合制得了以聚丙烯酸丁酯为核、苯乙烯-丙烯腈共聚物为壳的核壳接枝共聚物ASA;再以钛酸正四丁酯和偶联剂γ-(甲基丙烯酰氧基)丙基三甲氧基硅(KH-570)为原料,经水解缩合生成KH-570-g-TiO粒子.将ASA与KH-570-g-TiO粒子按照一定比例溶解并超声共混,在普通玻璃表面制得了ASA/TiO复合薄膜.用傅里叶变换红外光谱、热重分析、透射电镜及紫外可见光谱等对产物和薄膜进行了分析表征.结果显示,制得的ASA接枝共聚物具有明显的核壳结构,乳液粒子大小均匀,聚丙烯酸丁酯核的平均粒径为60 nm左右,壳的平均厚为20 nm.KH-570水解的羟基与纳米TiO表面的羟基发生了缩合反应.与纯ASA薄膜相比,ASA/TiO复合薄膜在紫外区的吸收更强,且最大吸收波长蓝移;复合薄膜的耐热性能要优于纯ASA薄膜,同时耐酸碱性能有所提高.%Butyl acrylate-styrene-acrylonitrile core-shell graft copolymer( ASA ) with poly( butyl acrylate ) as core and styrene-acrylonitrile copolymer as shell was synthesized by seeded emulsion polymerization, KH-570-g-TiO2 particle was prepared through hydrolysis condensation of coupling agent KH-570 and tetra-n-butyl titanate, and ASA and KH-570-g-TiO2 were blended with a certain ratio by ultrasonic mixing. Finally , the composite films were prepared on a glass substrate and characterized by Fourier transform-infrared spectroscopy, thermogravimetric analysis, transmission electron microscope and ultraviolet-visible spectroscopy. The results showed that the ASA graft copolymer had an obvious core-shell structure and the particle size of the emulsion was homogeneous. The average diameter of poly( butyl acrylate ) core was about 60 nm,and the shell thickness was about 20 nm. The condensation reaction occurred between the hydroxyl groups from the hydrolysis of KH-570 and on TiO2 surface. The ASA-TiO2 composite

  16. Simultaneous Determination of Acetaldehyde,Acrolein,Acrylonitrile and Pyridine in Water by Purge-and-trap-Gas Chromatography-Mass Spectrometry%吹扫捕集-气相色谱/质谱法测定水中的乙醛、丙烯醛、丙烯腈和吡啶

    Institute of Scientific and Technical Information of China (English)

    许家慧; 普学伟; 施艳峰; 觉玉峰

    2015-01-01

    水中的乙醛、丙烯醛、丙烯腈和吡啶经吹扫捕集、解吸后,用HP-VOC毛细管色谱柱进行GC分离,用GC-MS法选择离子模式( SIM)下进行检测,外标法定量。结果表明,选择取样量25 mL,吹扫流量为40 mL/min,吹扫温度为40℃,吹扫时间为15 min,解吸时间为2 min,解吸温度为200℃,烘焙时间20 min,乙醛和吡啶质量浓度在0.025~0.60 mg/L之间,丙烯醛和丙烯腈质量浓度在0.0025~0.10 mg/L之间时,校准曲线呈线性关系,相关系数r>0.995,乙醛、丙烯醛、丙烯腈和吡啶的方法检出限分别为0.0016,0.0013,0.0005和0.0021 mg/L。对3个不同浓度样品进行空白加标实验,测量的回收率为87.8%~114.3%,相对标准偏差(n=6)为2.51%~10.4%。对3批实际水样进行分析,其中一个废水水样加标回收率为79.2%~103.8%,相对标准偏差(n=6)为3.04%~6.39%。%A method for simultaneous determination of acetaldehyde,acrolein,acrylonitrile and pyridine in water by purge-and-trap-gas chromatography-mass spectrometry ( GC-MS) was reported.These compounds were concentrated by purging and trapping fol-lowed by desorption before GC-MS measurement using the HP-VOC capillary column for separation and selective ion mode ( SIM) for MS detection.External calibration was used for quantification.The following experimental conditions were used:the sampling vol-ume was 25 mL,purging gas flow was 40 mL/min,purging temperature was 40 ℃,purging time was 15 min,desorption time was 2 min,desorption temperature was 200℃,and baking time was 20 min.Under this condition,it was determined that the concentrations of acetaldehyde and pyridine were between 0.025 and 0.60 mg/L,and acrolein and acrylonitrile were between 0.002 5 and 0.10 mg/L.The calibration curve showed good linearity with the correlation coefficient r>0.995.The method detection limits of acetalde-hyde,acrolein,acrylonitrile

  17. Effects of Acrylonitrile on Gene Expression of Androgen Binding Protein and Inhibin in Testes of Spraque-Dawley Rats%丙烯腈对大鼠睾丸中雄激素结合蛋白和抑制素基因表达的影响

    Institute of Scientific and Technical Information of China (English)

    钟先玖; 吴鑫; 周元陵; 黄简抒; 金泰廙

    2005-01-01

    [目的]研究丙烯腈(acrylonitrile,ACN)对大鼠睾丸中雄激素结合蛋白(Androgen Binding Protein,ABP)和抑制素基因表达的影响.[方法]SD雄性大鼠随机分为4组,1组为对照组,另3组为染毒组,剂量分别为7.5、15.0和30.0 mg/kg体重,每天腹腔注射染毒1次,每周5次,连续13周,分别于4、8和13周末分批处死,取睾丸组织50~100mg,加1 ml Trizol磨成匀浆,加氯仿振摇,12 000 r/min,4℃下离心,取上清液,加异丙醇沉淀,75%乙醇洗涤,得到的RNA用紫外分光光度法测定其纯度,用一步法逆转录扩增(reverse transcription-polymerase chain reaction,RT-PCR)目的基因,用内参标进行半定量检测.[结果]ACN染毒未引起ABP和抑制素基因表达缺失.低、中剂量组睾丸中ABP和抑制素基因表达水平无明显变化.高剂量组,染毒4周后,ABP基因表达水平显著升高(P<0.05),染毒8周后下降,但与其他组无明显差异,13周后显著下降,与其他组有显著性差异(P<0.05).高剂量组染毒4周后,抑制素基因表达水平有下降趋势,且随染毒时间延长下降显著;中、高组在染毒8周后,抑制素基因表达水平下降显著,与对照组比较差异有显著性(P<0.01).[结论]ACN对大鼠睾丸中ABP和抑制素基因表达水平有影响,提示丙烯腈对睾丸中支持细胞可能有损伤作用.

  18. Study on the Preparation and Characterization of Flame-retardant Acrylonitrile-butadiene Rubber/Chlorinated Polypropylene Rubber-plastic Composites%阻燃型丁腈橡胶/氯化聚丙烯橡塑复合材料的制备与性能研究

    Institute of Scientific and Technical Information of China (English)

    彭军勇; 王曦; 苏胜培

    2012-01-01

    The flame-retardant acrylonitrile-butadiene rubber (NBR)/chlorinated polypropylene (CPP)rubber- plastic composites were prepared by adding antimony trioxide (Sb1O3) which is synergistic flame-retardant. The influences of the loading of Sb2O3 on curing characteristics, mechanical properties and flammability properties were evaluated. The experimental results showed that the processability of the blend system was not reduced with the increase of Sb2O3 loading. When the loading of Sb2O3 was at 10.0 phr., the tensile strength, 300% modulus and Shore A hardness of the composites were respectively improved by 15.7%, 112% and 10.9%. The limiting oxygen index (LOI) of the composites was increased with the increase of Sb2O3 loading. When the content of Sb2O3 was 2.5 phr, the LOI of the composites was up to 27.4%, which indicated that the inflammability of the composites was distinctly enhanced.%通过在丁腈橡胶(NBR)/氯化聚丙烯(CPP)橡塑复合材料中添加协同阻燃剂三氧化二锑,制备了阻燃型NBR/CPP橡塑复合材料,考察了三氧化二锑用量对NBR/CPP橡塑复合材料硫化特性、力学性能和燃烧性能的影响.实验结果表明:三氧化二锑的加入没有降低NBR/CPP橡塑复合材料的加工性能;当三氧化二锑用量为10.0份时,NBR/CPP橡塑复合材料的拉伸强度、300%定伸应力和邵氏硬度分别增加了15.7%、112%和10.9%;复合材料的氧指数(LOI)随三氧化二锑用量的增加逐渐增大,当三氧化二锑用量为2.5份时,复合材料氧指数为27.4%,达到自熄级阻燃效果.

  19. 热致相分离法制备丙烯腈-丙烯酸甲酯/纳米 TiO2复合膜及膜性能研究%Preparation and characterization of acrylonitrile-methyl acrylate/TiO2 composite membrane by thermally induced phase separation

    Institute of Scientific and Technical Information of China (English)

    王争争; 韩娜; 陈素梅; 张兴祥; 李伟

    2014-01-01

    以自制的可熔融丙烯腈(AN)-丙烯酸甲酯(MA)共聚物为基体,以碳酸乙烯酯(EC)与柠檬酸三乙酯(TEC)为复配稀释剂,采用热致相分离法(TIPS)制备丙烯腈-丙烯酸甲酯(AN-MA)/纳米二氧化钛(TiO2)复合膜。借助场发射扫描电子显微镜(FESEM)、X-射线衍射仪(XRD)和万能试验机,从微孔膜的力学性能、水通量、孔隙率、晶型等方面对膜的结构与性能进行表征。结果表明,添加 TiO2纳米粒子可以显著提高 AN-MA 微孔膜的机械强度和水通量。随着 TiO2含量的增加,微孔膜的机械强度先增加后降低,TiO2质量分数为0.1%时,断裂强度最高可达8.0 MPa,比未添加 TiO2的样品高36%。纳米 TiO2的加入一定程度上抑制了大孔的产生,微孔膜结构更加均一。随着凝固浴温度的升高,微孔膜的力学性能逐渐提高,通量出现下降趋势。%Acrylonitrile-methyl acrylate (AN-MA)/TiO2 composite membrane was prepared by thermally induced phase separa-tion (TIPS),using melt AN-MA copolymer as matrix,ethylene carbonate (EC)and triethyl citrate (TEC)as a complex diluent. With the help of field emission scanning electron microscope (FESEM),X-ray diffraction (XRD)and universal testing machine, the mechanical property,water flux,porosity and crystal form of the membrane were tested.The results show that the addition of TiO2 nanoparticles can significantly improve the mechanical strength and the water flux of AN-MA/TiO2 composite membrane. With the increase of TiO2 content,the mechanical strength of the composite membrane first increased and then decreased.When TiO2 mass fraction is 0.1%,the breaking strength of AN-MA/TiO2 composite membrane is up to 8.0 MPa,increased by 36%compared with pure AN-MA membrane.Addition of nano-TiO2 can suppress macrovoid to a certain degree,resulting in a more u-niform pore structure.With the coagulation bath temperature rising

  20. 丙烯腈诱导的氧化应激对大鼠睾丸NF-κB信号通路的影响%Effects of Oxidative Stress Induced via Acrylonitrile on NF-κB Signaling Pathway in Rats Testis

    Institute of Scientific and Technical Information of China (English)

    赵乾龙; 罗波艳; 潘丽; 魏倩; 张瑞萍; 党瑜慧; 李芝兰

    2016-01-01

    为探索丙烯腈(acrylonitrile,ACN)诱导的氧化应激对大鼠睾丸NF-κB信号通路的影响,将50只SPF级健康SD雄性大鼠按体重随机分为12.5、25、50 mg·kg-1 ACN染毒组,50 mg·kg-1 ACN+300 mg·kg-1 N-乙酰半胱氨酸(N-acetyleysteine,NAC)干预组(NAC干预组),对照组(给予等体积玉米油),每组10只,灌胃,1次/天,6天/周,共90 d.可见光分光光度法检测睾丸组织中超氧化物歧化酶(superoxide dismutase,SOD)、谷胱甘肽过氧化物酶(glutathione peroxidase,GSH-Px)、还原型谷胱甘肽/氧化型谷胱甘肽比值(glutathione/oxidized glutathione,GSH/GSSG)、丙二醛(malondialdehyde,MDA).免疫荧光染色法检测睾丸核因子-κB(nuclear factor κB,NF-κB)激活及核转移.Western Blot检测睾丸p65、IκB蛋白表达.结果显示,低、高剂量染毒组大鼠睾丸GSH/GSSG比值、GSH-Px酶活性与对照组比较降低(P,<0.05).中、高剂量染毒组大鼠睾丸MDA含量与对照组比较升高(P,<0.05).NAC干预组大鼠睾丸MDA含量与高ACN组比较降低(P<0.05);NAC干预组大鼠睾丸GSH/GSSG比值与高ACN组比较升高(P<0.05);免疫荧光结果显示,高ACN组大鼠睾丸NF-κB被激活,并转移入细胞核.NAC干预组与高ACN组比较p65蛋白表达及核转移显著减少.Western Blot结果显示,高剂量染毒组大鼠睾丸p65蛋白表达与对照组比较升高(P<0.05),IκB蛋白表达与对照组比较降低(P<0.05);NAC干预组大鼠睾丸p65蛋白表达与高ACN组比较降低,IκB蛋白表达与高ACN组比较升高,差异有统计学意义(P<0.05).结果表明丙烯腈引起的氧化应激激活了大鼠睾丸生殖细胞NF-κB信号通路.

  1. 吸水膨胀型丙烯腈-丁二烯-苯乙烯共聚物/丁腈橡胶热塑性硫化胶的性能及微观形貌%Properties and morphology of water-swellable acrylonitrile-butadiene-styrene copolymer/nitrile rubber thermoplastic vulcanizate

    Institute of Scientific and Technical Information of China (English)

    魏东亚; 何宁; 王兆波

    2015-01-01

    以交联聚丙烯酸钠(CPNaAA)为吸水材料,通过动态硫化法制备了基于丙烯腈-丁二烯-苯乙烯共聚物(ABS)/丁腈橡胶(NBR)/氯化聚乙烯(CM)热塑性硫化胶(TPV)的吸水膨胀橡胶(WSR),考察了 CPNaAA 用量对 WSR 物理机械性能和吸水性能的影响,研究了 WSR 的微观形貌。结果表明,在实验范围内,ABS/ NBR/ CM/ CPNaAA WSR 的应力-应变行为均表现出“软而韧”的弹性体特征,随着CPNaAA 用量的增加,WSR 的拉伸强度、扯断伸长率、永久变形和撕裂强度均呈下降趋势,邵尔 A 硬度略有提高,WSR 的吸水率、吸水速率及脱水失重率提高,当 CPNaAA 用量为70份时,室温下95 h WSR即达到吸水平衡状态,此时吸水率为369.8%;与第1次的最大吸水率相比,第2次及第3次的最大吸水率仅有小幅降低,但第2次及第3次的初始吸水速率远大于第1次的初始吸水速率,脱水失重率明显降低;CPNaAA 在 TPV 中分散均匀,未出现团聚现象,但表面结构松散,与 TPV 之间的界面作用较弱;WSR吸水干燥后表面出现明显的缝隙和孔洞。%The water-swellable rubber ( WSR) was pre-pared by dynamically vulcanization with acrylonitrile-butadi-ene-styrene copolymer/ nitrile rubber/ chlorinated polyethylene thermoplastic vulcanizate (TPV) as matrix and crosslinked po-ly( sodium acrylate) ( CPNaAA) as super water-absorbent. Effects of CPNaAA amount on the mechanical properties, wa-ter-swelling behavior and morphology of the prepared WSR were investigated. The results showed that all the stress -strain curves of the WSR behaved as a typical elastomer with soft and tough characters. With increasing CPNaAA, the ten-sile strength, elongation at break, permanent set and tear strength of the WSR decreased, Shore A hardness increased slightly, and the water-swelling ratio, water-swelling rate and mass loss increased significantly. Moreover, the WSR with 70 phr CPNaAA incorporation achieved the equilibrium swell

  2. SYNTHESIS OF ACRYLONITRILE-N-ISOPROPYLACRYLAMIDE GRAFT COPOLYMERS FOR THE PREPARATION OF THERMAL RESPONSIVE POLYACRYLONITRILE MEMBRANAES%丙烯腈-N-异丙基丙烯酰胺接枝共聚物的合成及其对聚丙烯腈分离膜的改性

    Institute of Scientific and Technical Information of China (English)

    费正东; 万灵书; 钟明强; 徐志康

    2012-01-01

    PNIPAAm with terminal amino groups was synthesized using 2-aminoethanethiol hydrochloride ( AESH) as a chain transfer agent. It was then reacted with methacryloyl chloride to result in macromer, vinly PNIPAAm. A graft copolymer,P( AN-g-NIPAAm) was synthesized through the copolymerization of acrylonitrile (AN) and vinyl PNIPAAm. Using this graft copolymer as an additive, thermal responsive PAN-based membranes were prepared by the immersion precipitation phase inversion method (IPPI). Results from FTIR and NMR indicate that the molecular weight of PNIPAAm can be effectively modulated by changing the concentration of AESH. Then, the weight average molecular weight ( Mw ) was measured by laser scattering. Results of captive bubble contact angle measurements and turbidity analysis show that the graft copolymers are still thermally responsive, which is more remarkable with higher PNIPAAm content. XPS analysis proves thatthe PNIPAAm graft chains are enriched at the membrane surface and pore surface during the course of IPPI because of the hydrophilicity of PNIPAAm. Pure water flux at 40℃ (above the LCST of PNIPAAm) is almost twice as that at 25℃ (below the LCST of PNIPAAm) ,which is due to the conformation change of PNIPAAm chains. All these results demonstrate the synthesized graft copolymers are effective additives for the preparation of thermal responsive PAN membranes.%以巯基乙胺盐酸盐( AESH)为链转移剂、2,2′-偶氮二异丁腈为引发剂,合成了具有端氨基的聚(N-异丙基丙烯酰胺)(PNIPAAm);与甲基丙烯酰氯反应,得到可聚合的PNIPAAm大分子单体;进而与丙烯腈共聚,合成了丙烯腈-N-异丙基丙烯酰胺接枝共聚物(P(AN-g-NIPAAm)).基于浸没沉淀相转化法制备了聚丙烯腈/P(AN-g-NIPAAm)共混膜.红外及核磁分析表明,通过调控AESH的浓度可制备得到不同链长的PNIPAAm大分子单体;用激光光散射进一步测定了共聚物的重均分子量;采用鼓泡接触角及浊度

  3. Solubility parameter of poly(styrene-co-acrylonitrile)

    Science.gov (United States)

    Wohlfarth, Ch.

    This document is part of Subvolume D2 'Polymer Solutions - Physical Properties and their Relations I (Thermodynamic Properties: PVT -Data and miscellaneous Properties of polymer Solutions) of Volume 6 `Polymers' of Landolt-Börnstein - Group VIII `Advanced Materials and Technologies'.

  4. From Green Aerogels to Porous Graphite by Emulsion Gelation of Acrylonitrile

    Science.gov (United States)

    2012-01-01

    of the corresponding aerogels were fitted with the Beaucage Unified Model46 as described for other organic aerogels recently.8,10b,47 While the...Lekner, J. Phys. Rev. 1966, 145, 83−90. (46) (a) Beaucage , G. J. Appl. Crystallogr. 1995, 28, 717−728. (b) Beaucage , G. J. Appl. Crystallogr. 1996, 29

  5. Coconut shell powder as cost effective filler in copolymer of acrylonitrile and butadiene rubber.

    Science.gov (United States)

    Keerthika, B; Umayavalli, M; Jeyalalitha, T; Krishnaveni, N

    2016-08-01

    Filler is one of the major additives in rubber compounds to enhance the physical properties. Even though numerous benefits obtained from agricultural by products like coconut shell, rice husk etc., still they constitute a large source of environmental pollution. In this investigation, one of the agricultural bye product coconut shell powder (CSP) is used as filler in the compounding KNB rubber. It shows the positive and satisfied result was achieved only by the use of filler Fast Extrusion Furnace (FEF) and coconut shell powder (CSP) which was used 50% in each. The effect of these fillers on the mechanical properties of a rubber material at various loading raging from 0 to 60PHP was studied. Mercaptodibanzothiazole disulphide (MBTS) was used as an accelerator. The result shows that presence of 25% and 50% of the composites has better mechanical properties like Hardness, Tensile strength, Elongation at break and Specific gravity when compared with other two combinations. Even though both 25% and 50% of composites shows good mechanical properties, 50% of CSP have more efficient than 25% of CSP.

  6. 76 FR 77267 - Acrylonitrile Standard; Extension of the Office of Management and Budget's (OMB) Approval of...

    Science.gov (United States)

    2011-12-12

    ... not publicly available to read or download through the Web site. All submissions, including... information is in the desired format, reporting burden (time and costs) is minimal, collection instruments are... operating small businesses, and to reduce to the maximum extent feasible unnecessary duplication of...

  7. 76 FR 38387 - Draft Toxicological Review of Acrylonitrile: In Support of Summary Information on the Integrated...

    Science.gov (United States)

    2011-06-30

    ... will need audio-visual equipment (e.g., laptop computer and slide projector). In general, each... p.m., Eastern Daylight Time, or when the last presentation has been completed. To attend the... and provide the length of your presentation. The following are instructions for registering: To...

  8. NONCONVENTIONAL EMULSION POLYMERIZATION OF ACRYLONITRILE CATALYZED BY in situ METAL COMPLEX

    Institute of Scientific and Technical Information of China (English)

    Bijayashree Samal; Prafulla K.Sahoo

    2007-01-01

    Nano-sized polyacrylonitrile (PAN) particles were prepared under the catalytic effect of in situ developed CoCl2/EDTA complex with ammonium persulfate as the initiator in the absence of any added emulsifier.The emulsion polymerization was studied at varying concentrations of the initiator,monomer,complex and solvent over a temperature range of 30-70℃.The overall activation energy(Ea,49.79 kJ/mol),energy of dissociation of initiator(Ed,82.68kJ/mol),number of micelles(0.163 × 1018)and the viscosity average molecular weight of the polymer were computed.The distribution of particle sizes was determined by transmission electron microscopy(TEM).It was found that the oil-in-water polymerization was stabilized by the presence of the CoCl2/EDTA in situ complex reducing the particle size into the nano order.The average diameters of PAN nano particles,obtained by TEM,were in the range of 50-150 nm at the maximum conversion.The experimental particle size was mainly dependent on the concentration of the complex and temperature.

  9. A comparison of the characteristics of excimer and femtosecond laser ablation of acrylonitrile butadiene styrene (ABS)

    Science.gov (United States)

    See, Tian Long; Liu, Zhu; Li, Lin; Zhong, Xiang Li

    2016-02-01

    This paper presents an investigation on the ablation characteristics of excimer laser (λ = 248 nm, τ = 15 ns) and femtosecond laser (λ = 800 nm, τ = 100 fs) on ABS polymer sheets. The laser-material interaction parameters (ablation threshold, optical penetration depth and incubation factor) and the changes in material chemical properties were evaluated and compared between the two lasers. The work shows that the ablation threshold and effective optical penetration depth values are dependent on the wavelength of laser beam (photon energy) and the pulse width. The ablation threshold value is lower for the excimer laser ablation of ABS (Fth = 0.087 J/cm2) than that for the femtosecond laser ablation of ABS (Fth = 1.576 J/cm2), demonstrating a more dominating role of laser wavelength than the pulse width in influencing the ablation threshold. The ablation depth versus the logarithmic scale of laser fluence shows two linear regions for the fs laser ablation, not previously known for polymers. The effective optical penetration depth value is lower for excimer laser ablation (α-1 = 223 nm) than that for femtosecond laser ablation (α-1 = 2917 nm). The ablation threshold decreases with increasing number of pulses (NOP) due to the chain scission process that shortens the polymeric chains, resulting in a weaker polymeric configuration and the dependency is governed by the incubation factor. Excimer laser treatment of ABS eliminates the Cdbnd C bond completely through the chain scission process whereas Cdbnd C bond is partially eliminated through the femtosecond laser treatment due to the difference in photon energy of the two laser beams. A reduction in the Cdbnd C bond through the chain scission process creates free radical carbons which then form crosslinks with each other or react with oxygen, nitrogen and water in air producing oxygen-rich (Csbnd O and Cdbnd O bond) and nitrogen-rich (Csbnd N) functional groups.

  10. Synthesis, Characterization and Photophysical Properties of Pyridine-Carbazole Acrylonitrile Derivatives

    Directory of Open Access Journals (Sweden)

    Gabriel Ramos-Ortiz

    2011-03-01

    Full Text Available We synthesized three novel highly fluorescent compounds, 2-(2’-pyridyl-3-(N-ethyl-(3’-carbazolylacrylonitrile, 2-(3”-pyridyl-3-(N-ethyl-(3’-carbazolylacrylonitrile, and 2-(4-pyridyl-3-(N-ethyl-(3’-carbazolylacrylonitrile by Knoevenagel condensation. The first two were synthesized without solvent in the presence of piperidine as a catalyst; the third was synthesized without a catalyst and with N,N-dimethylformamide as a solvent. In solution, the molar absorption coefficients showed absorptions at 380, 378, and 396 nm, respectively; in solid state, absorptions were at 398, 390, and 442 nm, respectively. The fluorescence emission was at 540, 540 and 604 nm, respectively, the 2-(4-pyridyl-3-(N-ethyl-(3’-carbazolylacrylonitrile showed a red shift in the emission of 64 nm compared to the other two compounds. The fluorescence quantum yield for the compounds in powder form showed values of 0.05, 0.14, and 0.006, respectively; compared with the value measured for the Alq3 reference, 2-(3”-pyridyl-3-(N-ethyl-(3’-carbazolylacrylonitrile had a lightly higher value. The third harmonic generation measurement for 2-(2’-pyridyl-3-(N-ethyl-(3’-carbazolylacrylonitrile yielded a χ(3 value of 5.5 × 10−12 esu, similar to that reported for commercial polymers.

  11. Molecular Imprinting Fibrous Membranes of Poly(acrylonitrile-co-acrylic acid) Prepared by Electrospinning

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    @@ Introduction Over the past few decades, molecular imprinting has been described as a technology for preparing "molecular doors" which can be matched to "template keys". It has been found to be a simple and effective approach to introduce specific recognition sites into synthetic polymers, namely, to create molecular imprinting polymers[1-4]. Remarkable features such as stability,ease of preparation and low cost, have made molecular imprinting polymers particularly attractive in chemical sensors, catalysis, drug delivery, and dedicated separations.

  12. A comparison of the characteristics of excimer and femtosecond laser ablation of acrylonitrile butadiene styrene (ABS)

    Energy Technology Data Exchange (ETDEWEB)

    See, Tian Long, E-mail: tianlong.see@postgrad.manchester.ac.uk [Corrosion and Protection Centre, School of Materials, The Mill, The University of Manchester, M13 9PL Manchester (United Kingdom); Laser Processing Research Centre, School of Mechanical, Aerospace and Civil Engineering, The University of Manchester, M13 9PL Manchester (United Kingdom); Liu, Zhu [Corrosion and Protection Centre, School of Materials, The Mill, The University of Manchester, M13 9PL Manchester (United Kingdom); Li, Lin [Laser Processing Research Centre, School of Mechanical, Aerospace and Civil Engineering, The University of Manchester, M13 9PL Manchester (United Kingdom); Zhong, Xiang Li [Corrosion and Protection Centre, School of Materials, The Mill, The University of Manchester, M13 9PL Manchester (United Kingdom)

    2016-02-28

    Highlights: • Ablation threshold for excimer laser is lower compared to femtosecond laser. • Effective optical penetration depth for excimer laser is lower compared to femtosecond laser. • Two ablation characteristic regimes are observed for femtosecond laser ablation. • Reduction of C=C bond following excimer or fs laser ablation is observed. • Addition of oxygen- and nitrogen-rich functional groups is observed. - Abstract: This paper presents an investigation on the ablation characteristics of excimer laser (λ = 248 nm, τ = 15 ns) and femtosecond laser (λ = 800 nm, τ = 100 fs) on ABS polymer sheets. The laser–material interaction parameters (ablation threshold, optical penetration depth and incubation factor) and the changes in material chemical properties were evaluated and compared between the two lasers. The work shows that the ablation threshold and effective optical penetration depth values are dependent on the wavelength of laser beam (photon energy) and the pulse width. The ablation threshold value is lower for the excimer laser ablation of ABS (F{sub th} = 0.087 J/cm{sup 2}) than that for the femtosecond laser ablation of ABS (F{sub th} = 1.576 J/cm{sup 2}), demonstrating a more dominating role of laser wavelength than the pulse width in influencing the ablation threshold. The ablation depth versus the logarithmic scale of laser fluence shows two linear regions for the fs laser ablation, not previously known for polymers. The effective optical penetration depth value is lower for excimer laser ablation (α{sup −1} = 223 nm) than that for femtosecond laser ablation (α{sup −1} = 2917 nm). The ablation threshold decreases with increasing number of pulses (NOP) due to the chain scission process that shortens the polymeric chains, resulting in a weaker polymeric configuration and the dependency is governed by the incubation factor. Excimer laser treatment of ABS eliminates the C=C bond completely through the chain scission process whereas C=C bond is partially eliminated through the femtosecond laser treatment due to the difference in photon energy of the two laser beams. A reduction in the C=C bond through the chain scission process creates free radical carbons which then form crosslinks with each other or react with oxygen, nitrogen and water in air producing oxygen-rich (C−O and C=O bond) and nitrogen-rich (C−N) functional groups.

  13. Resistivity and Its Anisotropy Characterization of 3D-Printed Acrylonitrile Butadiene Styrene Copolymer (ABS/Carbon Black (CB Composites

    Directory of Open Access Journals (Sweden)

    Jie Zhang

    2017-01-01

    Full Text Available The rapid printing of 3D parts with desired electrical properties enables numerous applications. Fused deposition modeling (FDM using conductive thermoplastic composites has been a valuable approach for such fabrication. The parts produced by FDM possess various controllable structural features, but the effects of the structural features on the electrical properties remain to be determined. This study investigated the effects of these features on the electrical resistivity and resistivity anisotropy of 3D-printed ABS/CB composites. The effects of the process parameters of FDM, including the layer thickness, raster width, and air gap, on the resistivity in both the vertical and horizontal directions for cubic samples were studied because the internal structure of the printed parts depended on those process parameters. The resistivities of printed parts in different parameter combinations were measured by an impedance analyzer and finite element models were created to investigate the relationship between the resistivity and the internal structure. The results indicated that the parameters remarkably affected the resistivity due to the influence of voids and the bonding condition between adjacent fibers. The resistivity in the vertical direction ranged from 70.40 ± 2.88 Ω·m to 180.33 ± 8.21 Ω·m, and the resistivity in the horizontal direction ranged from 41.91 ± 2.29 Ω·m to 58.35 ± 0.61 Ω·m at the frequency of 1 kHz. Moreover, by adjusting the resistivities in different directions, the resistivity anisotropy of the printed parts can be manipulated from 1.01 to 3.59. This research may serve as a reference to fabricate parts with sophisticated geometry with desired electrical resistivity and resistivity anisotropy.

  14. Conformational and Molecular Structures of α,β-Unsaturated Acrylonitrile Derivatives: Photophysical Properties and Their Frontier Orbitals

    OpenAIRE

    María Judith Percino; Margarita Cerón; Oscar Rodríguez; Guillermo Soriano-Moro; María Eugenia Castro; Chapela, Víctor M.; Siegler, Maxime A.; Enrique Pérez-Gutiérrez

    2016-01-01

    We report single crystal X-ray diffraction (hereafter, SCXRD) analyses of derivatives featuring the electron-donor N-ethylcarbazole or the (4-diphenylamino)phenyl moieties associated with a -CN group attached to a double bond. The compounds are (2Z)-3-(4-(diphenylamino)-phenyl)-2-(pyridin-3-yl)prop-2-enenitrile (I), (2Z)-3-(4-(diphenylamino)phenyl)-2-(pyridin-4-yl)-prop-2-enenitrile (II) and (2Z)-3-(9-ethyl-9H-carbazol-3-yl)-2-(pyridin-2-yl)enenitrile (III). SCXRD analyses reveal that I and I...

  15. THE EFFECTS OF N-2-HYDROXYETHYL-N-METHYL-P-TOLUIDINE ON METHYL METHACRYLATE RADICAL POLYMERIZATION AND ACRYLONITRILE PHOTOINDUCED POLYMERIZATION

    Institute of Scientific and Technical Information of China (English)

    QIU Kunyuan; ZHANG Zhanghua; FENG Xinde

    1992-01-01

    The effects of N-2-hydroxyethyl-N-methyl-p-toluidine (HMT) on MMA polymerization using organic peroxide as an initiator and on AN photoinduced polymerization have been investigated respectively. The kinetics of polymerization and the overall activation energy of polymerization were determined. Based on kinetics study and the end group analysis of the polymer obtained by UV spectrum method, the initiation mechanism is proposed.

  16. Thermal behavior of vehicle plastic blends contained acrylonitrile-butadiene-styrene (ABS) in pyrolysis using TG-FTIR.

    Science.gov (United States)

    Liu, Guicai; Liao, Yanfen; Ma, Xiaoqian

    2017-03-01

    As important plastic blends in End-of-Life vehicles (ELV), pyrolysis profiles of ABS/PVC, ABS/PA6 and ABS/PC were investigated using thermogravimetric-Fourier transform infrared spectrometer (TG-FTIR). Also, CaCO3 was added as plastic filler to discuss its effects on the pyrolysis of these plastics. The results showed that the interaction between ABS and PVC made PVC pyrolysis earlier and HCl emission slightly accelerated. The mixing of ABS and PA6 made their decomposition temperature closer, and ketones in PA6 pyrolysis products were reduced. The presence of ABS made PC pyrolysis earlier, and phenyl compounds in PC pyrolysis products could be transferred into alcohol or H2O. The interaction between ABS and other polymers in pyrolysis could be attributed to the intermolecular radical transfer, and free radicals from the polymer firstly decomposed led to a fast initiation the decomposition of the other polymer. As plastic filler, CaCO3 promoted the thermal decomposition of PA6 and PC, and had no obvious effects on ABS and PVC pyrolysis process. Also, CaCO3 made the pyrolysis products from PA6 and PC further decomposed into small-molecule compounds like CO2. The kinetics analysis showed that isoconversional method like Starink method was more suitable for these polymer blends. Starink method showed the average activation energy of ABS50/PVC50, ABS50/PA50 and ABS50/PC50 was 186.63kJ/mol, 239.61kJ/mol and 248.95kJ/mol, respectively, and the interaction among them could be reflected by the activation energy variation.

  17. Effect of winding layer and speed on kenaf/glass fiber hybrid reinforced acrylonitrile butadiene styrene (ABS) composites

    Science.gov (United States)

    Khoni, Norizzahthul Ainaa Abdul; Sharifah Shahnaz S., B.; Ghazali, Che Mohd Ruzaidi

    2016-07-01

    The usage of natural fiber is becoming significant in composite industries due to their good performance. Single and continuous natural fibers have relatively high mechanical properties; especially their young modulus can be as high as glass fibers. Filament winding is a method to produce technically aligned composites which have high fibers content. The properties of filament winding can be tailored to meet the end product requirements. This research studied the compression properties of kenaf/glass fibers hybrid reinforced composites. Kenaf/glass fibers hybrid composite samples were fabricated by filament winding technique and their properties were compared with the properties of neat kenaf fiber and glass fibers composites. The kenaf/glass fiber hybrid composites exhibited higher strength compared to the neat glass fibers composites. Composites of helical pattern, which produced at low winding speed showed better compression resistance than hoop pattern winding, which produced at high winding speed. As predicted, kenaf composite showed highest water absorption; followed by kenaf/glass fiber hybrid composites while neat glass fiber has lowest water absorption capability.

  18. Conformational and Molecular Structures of α,β-Unsaturated Acrylonitrile Derivatives: Photophysical Properties and Their Frontier Orbitals

    Directory of Open Access Journals (Sweden)

    María Judith Percino

    2016-03-01

    Full Text Available We report single crystal X-ray diffraction (hereafter, SCXRD analyses of derivatives featuring the electron-donor N-ethylcarbazole or the (4-diphenylaminophenyl moieties associated with a -CN group attached to a double bond. The compounds are (2Z-3-(4-(diphenylamino-phenyl-2-(pyridin-3-ylprop-2-enenitrile (I, (2Z-3-(4-(diphenylaminophenyl-2-(pyridin-4-yl-prop-2-enenitrile (II and (2Z-3-(9-ethyl-9H-carbazol-3-yl-2-(pyridin-2-ylenenitrile (III. SCXRD analyses reveal that I and III crystallize in the monoclinic space groups P2/c with Z’ = 2 and C2/c with Z’ = 1, respectively. Compound II crystallized in the orthorhombic space group Pbcn with Z’ = 1. The molecular packing analysis was conducted to examine the pyridine core effect, depending on the ortho, meta- and para-positions of the nitrogen atom, with respect to the optical properties and number of independent molecules (Z’. It is found that the double bond bearing a diphenylamino moiety introduced properties to exhibit a strong π-π-interaction in the solid state. The compounds were examined to evaluate the effects of solvent polarity, the role of the molecular structure, and the molecular interactions on their self-assembly behaviors. Compound I crystallized with a cell with two conformers, anti and syn, due to interaction with solvent. DFT calculations indicated the anti and syn structures of I are energetically stable (less than 1 eV. Also electrochemical and photophysical properties of the compounds were investigated, as well as the determination of optimization calculations in gas and different solvent (chloroform, cyclohexane, methanol, ethanol, tetrahydrofuran, dichloromethane and dimethyl sulfoxide in the Gaussian09 program. The effect of solvent by PCM method was also investigated. The frontier HOMO and LUMO energies and gap energies are reported.

  19. Conformational and Molecular Structures of α,β-Unsaturated Acrylonitrile Derivatives: Photophysical Properties and Their Frontier Orbitals.

    Science.gov (United States)

    Percino, María Judith; Cerón, Margarita; Rodríguez, Oscar; Soriano-Moro, Guillermo; Castro, María Eugenia; Chapela, Víctor M; Siegler, Maxime A; Pérez-Gutiérrez, Enrique

    2016-03-28

    We report single crystal X-ray diffraction (hereafter, SCXRD) analyses of derivatives featuring the electron-donor N-ethylcarbazole or the (4-diphenylamino)phenyl moieties associated with a -CN group attached to a double bond. The compounds are (2Z)-3-(4-(diphenylamino)-phenyl)-2-(pyridin-3-yl)prop-2-enenitrile (I), (2Z)-3-(4-(diphenylamino)phenyl)-2-(pyridin-4-yl)-prop-2-enenitrile (II) and (2Z)-3-(9-ethyl-9H-carbazol-3-yl)-2-(pyridin-2-yl)enenitrile (III). SCXRD analyses reveal that I and III crystallize in the monoclinic space groups P2/c with Z' = 2 and C2/c with Z' = 1, respectively. Compound II crystallized in the orthorhombic space group Pbcn with Z' = 1. The molecular packing analysis was conducted to examine the pyridine core effect, depending on the ortho, meta- and para-positions of the nitrogen atom, with respect to the optical properties and number of independent molecules (Z'). It is found that the double bond bearing a diphenylamino moiety introduced properties to exhibit a strong π-π-interaction in the solid state. The compounds were examined to evaluate the effects of solvent polarity, the role of the molecular structure, and the molecular interactions on their self-assembly behaviors. Compound I crystallized with a cell with two conformers, anti and syn, due to interaction with solvent. DFT calculations indicated the anti and syn structures of I are energetically stable (less than 1 eV). Also electrochemical and photophysical properties of the compounds were investigated, as well as the determination of optimization calculations in gas and different solvent (chloroform, cyclohexane, methanol, ethanol, tetrahydrofuran, dichloromethane and dimethyl sulfoxide) in the Gaussian09 program. The effect of solvent by PCM method was also investigated. The frontier HOMO and LUMO energies and gap energies are reported.

  20. Electrospinning of Poly[acrylonitrile-co-(glycidyl methacrylate)] Nanofibrous Mats for the Immobilization of Candida Antarctica Lipase B

    NARCIS (Netherlands)

    Dai, Tianhe; Miletic, Nemanja; Loos, Katja; Elbahri, Mady; Abetz, Volker; Miletić, Nemanja

    2011-01-01

    PANGMA nanofibers and nanomats with fiber diameters of 200-300 nanometers were fabricated by electrospinning. Cal-B was covalently immobilized onto the PANGMA nanomats via three different immobilization routes. The properties of the Cal-B-immobilized PANGMA nanomats were assayed and compared with th

  1. (Z-2-(4-{[(E-2-Hydroxybenzylidene]amino}phenyl-3-[4-(1,4,7,10-tetraoxa-13-azacyclopentadecan-13-ylphenyl]acrylonitrile

    Directory of Open Access Journals (Sweden)

    Xin Zhang

    2016-10-01

    Full Text Available The title compound, C32H35N3O5, is an important fluorescence probe. It is composed of a 1,4,7,10-tetraoxa-13λ2-azacyclopentadecane unit linked to a twisted (Z-2-(4-{[(E-2-hydroxybenzylidene]amino}phenyl-3-phenylacrylonitrile chain. In the molecule, an O—H...N hydrogen bond forms an S(6 ring motif. There is also in intramolecular C—H...N hydrogen bond in the azacrown ether moiety, which also forms an S(6 ring motif. In the crystal, molecules are linked via pairs of C—H...O hydrogen bonds, forming inversion dimers.

  2. Phase Partition of Acrylonitrile (AN) in Vinylidene Chloride (VDC)/Water System and Its Effect on VDC-AN Copolymer Composition

    Institute of Scientific and Technical Information of China (English)

    周树学; 翁志学; 黄志明; 潘祖仁

    1999-01-01

    phase partition of acrylvnitrile in the vlnylidene chloride/water system at different temperature and under pressure was studied, A calculation method for average VDC-AN copolymer compeeition with AN phmm partition considered was proposed. The conversion results are in good agreement with the experimental data nearly the entire conversion rauge. VDC-AN copolymer with narrower composltion distribution can be prepared in the suspension process and interpreted with dynamic equilibrium of AN between the oil and water phases continuously.

  3. 丙烯腈对蝾螈睾丸精原细胞DNA的诱导损伤%DNA Damage on Newt Testicle Spermatogonia Induced by Acrylonitrile

    Institute of Scientific and Technical Information of China (English)

    黄简抒; 吴鑫; 钟先玖

    2006-01-01

    目的探讨丙烯腈(ACN)对睾丸精原细胞DNA的损伤作用及经肝微粒体酶活化前后该损伤程度的差异.方法用体外培养方法分离蝾螈睾丸精原细胞,不同浓度(0,0.1,0.4,0.8,1.6 μmol/ml)ACN染毒3 h,每个浓度分活化组(加S9)和非活化组(不加S9),另设2个阳性对照组(丝裂霉素C,1.6μg/ml,加S9)和(环磷酰胺,80μg/ml,不加S9),用单细胞凝胶电泳法检测DNA损伤程度.结果未活化ACN浓度≥0.8μmol/ml及活化后ACN浓度≥0.4 μmol/ml时,蝾螈精原细胞DNA损伤程度明显升高,彗星发生率、长尾彗星率及彗星细胞平均尾长均明显高于对照组(P<0.05),并存在剂量-反应关系,经S9活化后,ACN对DNA损伤程度比同浓度未活化组明显增强.结论ACN能诱导蝾螈睾丸精原细胞DNA损伤,并且经肝微粒体酶活化后损伤能力明显增强.

  4. Preparation of 1,3-Disubstituted-5-cyano-4,5-dihydropyrazoles via 1,3-Dipolar Cycloaddition of Nitrile Imine with Acrylonitrile

    Institute of Scientific and Technical Information of China (English)

    SONG,Li-Ping(宋力平); ZHU,Shi-Zheng(朱士正); HUANG,Ji-Ling(黄吉玲)

    2002-01-01

    Oxidation of aldehyde 4-chloro-2, 3, 5, 6-tetrafluorophhenylhydrazones (1) with [bis(acetoxy)iodo]benzene leads to the formation of nitrile imines (2) which can react in situ with acryloniprile to produce 1-(4-chloro-2, 3, 5, 6-tetrafluorophenyl)-3-substituted-5-cyano-4, 5-dihydropyrazoles (3) in moderate to good yields. The structures of new compounds were fully confirmed by their spectral data and elemental analyses. A plausible reaction mechanism for the generation of nitrile imine is proposed.

  5. 丙烯腈对小鼠睾丸组织形态学的影响%Influence of acrylonitrile on morphology of testicle tissue in mice

    Institute of Scientific and Technical Information of China (English)

    肖卫; 刘小宁

    2006-01-01

    丙烯腈对雄性小鼠生殖系统具有细胞毒作用,我们通过雄性小鼠腹腔注射染毒,光镜结合病理图像分析仪定量测定,探讨丙烯腈染毒后小鼠睾丸组织学形态改变.

  6. The reaction of the acrylonitrile ion CH 2dbnd CH-C tbnd N rad + with HCN: Proton-transport catalysis vs formation of ionized pyrimidine

    Science.gov (United States)

    Ervasti, Henri K.; Jobst, Karl J.; Gerbaux, Pascal; Burgers, Peter C.; Ruttink, Paul J. A.; Terlouw, Johan K.

    2009-11-01

    The CBS-QB3 model chemistry predicts that the title ion-molecule reaction, of potential interest in astrochemistry, yields a stable head-to-tail dimer, [HC dbnd N-CH 2C(H)C tbnd N] rad + ( D1). Cyclization of D1 into ionized pyrimidine seems possible, but the initiating 1,2-H shift is close in energy to back-dissociation into CH 2dbnd C(H)CN rad + ( AN) + HCN. Less energy demanding is formation of the H-bridged isomers [CH 2dbnd C(CN)H--N tbnd CH] rad + and [HC tbnd N--HC(H) dbnd C(H)CN] rad +, whose HCN component may catalyze isomerization of AN into CH 2dbnd C dbnd C dbnd NH rad + ( AN1) and CH dbnd C(H)C dbnd NH rad + ( AN2) respectively. Tandem mass spectrometry based experiments using 15N/ 13C labelling show that cyclization of D1 does not occur and that AN1 is the predominant reaction product instead.

  7. Preparation and Characterization of a Hybrid Solid Polymer Electrolyte Consisting of Poly(Ethyleneoxide) and Poly(Acrylonitrile) for Polymer-Battery Application

    OpenAIRE

    Nookala, Munichandraiah; Scanlon, Lawrence G; Marsh, Richard A

    1997-01-01

    For application in an ambient temperature solid state lithium battery a highly dimensionally-stable polymer electrolyte based on polyethyleneoxide (PEO) suffers from low ionic conductivity, whereas a highly conducting gel electrolyte based on polyacrylonitrile (PAN) suffers from low dimensional stability. In order to overcome these problems, a hybrid solid polymer electrolyte (HSPE) was prepared using PEO, PAN, propylene carbonate (PC), ethylene carbonate (EC) and lithium perchlorate. The HSP...

  8. Morphology and contact angle studies of poly(styrene-co-acrylonitrile modified epoxy resin blends and their glass fibre reinforced composites

    Directory of Open Access Journals (Sweden)

    2007-06-01

    Full Text Available In this study, the surface characteristics of blends and composites of epoxy resin were investigated. Poly(styrene-co-acylonitrile (SAN was used to modify diglycedyl ether of bisphenol-A (DGEBA type epoxy resin cured with diamino diphenyl sulfone (DDS and the modified epoxy resin was used as the matrix for fibre reinforced composites (FRP’s. E-glass fibre was used as the fibre reinforcement. The scanning electron micrographs of the fractured surfaces of the blends and composites were analyzed. Morphological analysis revealed different morphologies such as dispersed, cocontinuous and phase-inverted structures for the blends. Contact angle studies were carried out using water and methylene iodide at room temperature. The solid surface energy was calculated using harmonic mean equations. Blending of epoxy resin increases its contact angle. The surface free energy, work of adhesion, interfacial free energy, spreading coefficient and Girifalco-Good’s interaction parameter were changed significantly in the case of blends and composites. The incorporation of thermoplastic and glass fibre reduces the wetting and hydrophilicity of epoxy resin.

  9. Performance of CTBN(carboxyl-terminated poly (butadiene-co-acrylonitrile))-EP(diglycidyl ether of bisphenol-A(DGEBA)) Prepolymers and CTBN-EP/polyetheramine (PEA) System

    Institute of Scientific and Technical Information of China (English)

    SHI Minxian; HUANG Zhixiong; LI Yaming; YANG Guorui

    2009-01-01

    CTBN-EP prepolymers were synthesized from CTBN and epoxy resin under the catalysis of HTMAB.FTIR analyses indicate the formation of ester group between the carboxyl group of CTBN and the oxirane group of epoxy resin.The viscosity of modified prepolymer increases with CTBN content increasing,but the epoxy value of the prepolymer decreases greatly.DSC analyses verify that CTBN affects the curing process of CTBN-EP/PEA system.Mechanical testing presents the improved toughness of CTBN-EP/PEA curings for the decrease of tensile strength,flexural strength and compressive strength,and increase of impact strength and elongation-at-break with the CTBN content increasing.SEM micrographs show the rubber phase with many holes in diameter about 0.5-1.5μm is formed when CTBN content is lower than 10 phr.However,the pattern of SEM graph shows some stalactite-like strips when CTBN content is higher than 15 phr.Furthermore,the SEM image of 25 phr CTBN sample forms a kind of co-continuous structure.

  10. Poly (vinylidene fluoride) / Poly (acrylonitrile)-based Superior Hydrophobic Piezoelectric Solid Derived by Aligned Carbon Nanotube in Electrospinning: Fabrication, the Phase Conversion and Surface Energy.

    Science.gov (United States)

    Aqeel, Salem M; Wang, Zhe; Than, Lisa; Sreenivasulu, Gollapudi; Zeng, Xiangqun

    2015-01-01

    Multifunctional materials have attracted many interests from both fundamental and practical aspects, such as field-effect transistor, electric protection, transducers and biosensor. Here we demonstrated the first superior hydrophobic piezoelectric surface based on the polymer blend of polyvinylidene fluoride (PVDF)-polyacrilonitrile (PAN) assisted with functionalized multiwalled nanotubes (MWNTs), by a modified electrospinning method. Typically the β-phase polyvinylidene fluoride (PVDF) was considered as the excellent piezoelectric and pyroelectric materials. However, polar β-phase of PVDF exhibited a natural high hydrophilicity. As a well-known fact, the wettability of the surface is dominated by two major factors: surface composition and surface roughness. The significant conversions derived by the incorporation of MWNTs, from nonpolar α-phase to highly polar β-phase of PVDF, were confirmed by FTIR. Meanwhile, the effects of MWNTs on the improvement of the roughness and the hydrophobicity of polymer blend were evaluated by atomic force microscopy (AFM) and contact angle (CA). Molar free energy of wetting of the polymer nanocomposite decreases with increasing the wt.% of MWNTs. All molar free energy of wetting of PVDF-PAN/MWNTs were negative, which means the non-wettability of film. The combination of surface roughness and low-surface-energy modification in nanostructured composites leads to high hydrophobicity. Particularly, fabrication of superior hydrophobic surfaces not only has fundamental interest but also various possible functional applications in micro- and nano-materials and devices.

  11. Poly (vinylidene fluoride) / Poly (acrylonitrile)–based Superior Hydrophobic Piezoelectric Solid Derived by Aligned Carbon Nanotube in Electrospinning: Fabrication, the Phase Conversion and Surface Energy

    Science.gov (United States)

    Aqeel, Salem M.; Than, Lisa; Sreenivasulu, Gollapudi

    2015-01-01

    Multifunctional materials have attracted many interests from both fundamental and practical aspects, such as field–effect transistor, electric protection, transducers and biosensor. Here we demonstrated the first superior hydrophobic piezoelectric surface based on the polymer blend of polyvinylidene fluoride (PVDF)–polyacrilonitrile (PAN) assisted with functionalized multiwalled nanotubes (MWNTs), by a modified electrospinning method. Typically the β–phase polyvinylidene fluoride (PVDF) was considered as the excellent piezoelectric and pyroelectric materials. However, polar β–phase of PVDF exhibited a natural high hydrophilicity. As a well–known fact, the wettability of the surface is dominated by two major factors: surface composition and surface roughness. The significant conversions derived by the incorporation of MWNTs, from nonpolar α–phase to highly polar β–phase of PVDF, were confirmed by FTIR. Meanwhile, the effects of MWNTs on the improvement of the roughness and the hydrophobicity of polymer blend were evaluated by atomic force microscopy (AFM) and contact angle (CA). Molar free energy of wetting of the polymer nanocomposite decreases with increasing the wt.% of MWNTs. All molar free energy of wetting of PVDF–PAN/MWNTs were negative, which means the non–wettability of film. The combination of surface roughness and low–surface–energy modification in nanostructured composites leads to high hydrophobicity. Particularly, fabrication of superior hydrophobic surfaces not only has fundamental interest but also various possible functional applications in micro– and nano–materials and devices. PMID:26989486

  12. Effect of using batch or semi-batch reactor on the chemical composition distribution of styrene-maleic anhydride-acrylonitrile terpolymers

    OpenAIRE

    Cunha, Regina de J. S.; Ailton S. Gomes

    1997-01-01

    Texto completo: acesso restrito. p.595-600 The influence of the reactor type on distribution of chemical composition of STY AN/MA terpolymers obtained by free-radical polymerization is shown. When a batch reactor was used we have obtained polymers with broad chemical composition distribution. However, if a semi-batch reactor with appropriate addition protocol was used it can be possible to synthesize terpolymers with homogeneous chemical composition.

  13. Electrospun Poly(acrylonitrile-co-acrylic acid) Nanofibrous Membranes for Catalase Immobilization:Effect of Porphyrin Filling on the Enzyme Activity

    Institute of Scientific and Technical Information of China (English)

    KE Bei-bei; WAN Ling-shu; HUANG Xiao-jun; XU Zhi-kang

    2011-01-01

    Porphyrin-filled nanofibrous membranes were facilely prepared by electrospinning of the mixtures of poly(acryionitrile-co-acrylic acid)(PANCAA) and porphyrins. 5,10,15,20-Tetraphenyiporphyrin(TPP) and its metalloderivatives(ZnTPP and CuTPP) were studied as filling mediators for the immobilization of redox enzyme. Results indicate that the introduction of TPP, ZnTPP and CuTPP improves the retention activity of the immobilized catalase.Among these three porphyrins, the ZnTPP-filled PANCAA nanofibrous membrane exhibits an activity retention of 93%, which is an exciting improvement. This improvement is attributed to both the strong catalase-porphyrin affinity and the possible facilitated electron transfer induced by the porphyrin as evidenced by quartz crystal microbalance (QCM) and fluorescence spectroscopy studies.

  14. Morphology Structure and Properties of Hydrogenated Acrylonitrile Butadiene Rubber/Ultra-Fine Full-Vulcanized Acrylonitrile Butadiene Rubber Powder Blends%氢化丁腈橡胶/超细全硫化粉末丁腈橡胶共混物的结构与性能研究

    Institute of Scientific and Technical Information of China (English)

    刘俊杰; 张立群; 刘力; 高富强; 肖大玲; 卢咏来

    2009-01-01

    采用熔融共混工艺制备了氢化丁腈橡胶(HNBR)/超细全硫化粉末丁腈橡胶(UFPNBR)共混物,研究了共混物相态结构、动态力学性能、力学性能及老化性能,并与HNBR/NBR共混物作了对比.透射电镜观察表明:在HNBR/UFPNBR体系中,HNBR容易形成连续相,UFPNBR为分散相;在HNBR/NBR体系中容易形成双连续相结构. DMA动态力学性能分析表明:2种共混物都只有一个tanδ峰,且相容性较好.HNBR/UFPNBR共混物在玻璃化转变区的tanδ峰值逐渐降低,而HNBR/NBR体系的tanδ峰值先减小后增大.加入适量的UFPNBR能降低HNBR/UFPNBR共混物的压缩永久变形;与常规共混胶相比,HNBR/UFPNBR具有低脆性温度和良好的耐老化性能,但力学性能略低.

  15. Toxicity of Acrylonitrile (ACN) on Rat Sertoli Cells in Primary Dual-chamber Culture%丙烯腈对原代双室培养的大鼠睾丸支持细胞的毒性

    Institute of Scientific and Technical Information of China (English)

    钟先玖; 吴鑫; 韩志英; 钱海雷; 金泰廙

    2006-01-01

    [目的]研究丙烯腈(ACN)对原代双室培养的大鼠睾丸支持细胞(Sertoli cell,Sc)的毒性,以探讨ACN诱导雄性生殖毒性机制.[方法]用已分离纯化的大鼠睾丸SC为材料,用原代双室培养方法,加和不加S9,以浓度为0、0.5、5.0、25.0μg/ml ACN染毒,于4、12、24、48 h后检测跨细胞上皮电阻(TER);染毒24、48 h后检测转铁蛋白(Trf)浓度,评价ACN体外染毒对大鼠睾丸SC的损伤.[结果]ACN浓度≥5.0μg/ml时,对TER的形成有明显抑制作用;5.0 μg/ml培养48 h、25.0μg/ml培养12 h后对已形成的TER引起下降;加S9(+S9)与不加S9(-S9),TER值接近(如25.0 μg/ml组培养12 h后+S9组为480.3,-S9组为486.3),无明显差异.浓度为25.0μg/ml时,ACN染毒引起外室Trf浓度升高,明显高于对照及其他组(P<0.05),内室Trf浓度变化不明显,因此内室与外室之间Trf浓度差值缩小.[结论]结果表明ACN对双室培养的SCTER的形成有抑制作用,对已形成的TER有降低作用;提示ACN可能对SC形成的紧密连接和"血睾屏障"有影响.

  16. 丙烯腈对雄性大小鼠血清中性激素水平的影响%Effects of Acrylonitrile on Levels of Sexual Hormone in Sera of Rats and Mice

    Institute of Scientific and Technical Information of China (English)

    黄简抒; 吴鑫; 钟先玖

    2005-01-01

    目的通过研究丙烯腈(ACN)对雄性大鼠、小鼠生殖性激素水平的影响,探讨ACN诱导生殖毒性的可能机制.方法选用ICR和昆明种小鼠用不同剂量的ACN(0,6.0,12.0,24.0 mg/kg)灌胃染毒8周,选用SD雄性大鼠用不同剂量的ACN(0,7.5,15.0,30.0 mg/kg)腹腔注射染毒13周,用放射免疫分析法(RIA)检测血清中睾酮(T)及雌二醇(E\\-2)水平;选用出生后22~25 d的SD雌性大鼠,一次性腹腔注射不同剂量的ACN(5.0,15.0,30.0 mg/kg)染毒,设阴性对照组(溶剂)和阳性对照组(β-雌二醇,剂量30 μg/kg), 染毒后6 h取子宫称重.结果 ACN染毒8周后,ICR小鼠血清中T水平均低于对照组,高剂量组与对照组比较差异有显著性(P<0.01); 昆明种小鼠血清中T水平也降低,中剂量组与对照组比较,差异有显著性(P<0.05).大鼠ACN染毒13周后,低剂量组E\\-2水平明显高于对照组(P<0.05),高剂量组T水平和E\\-2水平明显低于低剂量组(P<0.05), 但与对照组比较差异无显著性.雌性SD大鼠染毒后,各剂量组子宫重量与阴性对照组之间差异无显著性,但明显低于阳性对照组.结论 ACN能诱导雄性大鼠、小鼠血清性激素水平改变,对雄性大鼠、小鼠生殖内分泌系统有影响,在本实验条件下ACN没有出现雌激素样作用.

  17. Effect of Acrylonitrile Exposure on Reproductive Outcomes of Fathers and Parents%父亲和双亲接触丙烯腈对生殖结局的影响

    Institute of Scientific and Technical Information of China (English)

    王婷; 尚慧; 张建华; 郭宝清; 李林云

    2003-01-01

    目的探讨丙烯腈(ACN)对男女工生殖功能的影响.方法选择510名接触ACN作业工人,其中331名男工为父亲接触组,179人为双亲接触组,另选无ACN接触史的男工503人为对照组,比较女方的生殖结局.同时进行动物实验,小鼠静式吸入ACN,处死后取附睾检查精子畸变率.结果对接触组与对照组配偶生殖结局调查结果的比较发现,其过期产数、周岁患病例数差异均有显著性,但子代出生缺陷差异无显著性.父亲接触组和双亲接触组女方生殖结局调查结果的比较发现,其不孕率差异有显著性.动物实验结果显示,吸入ACN后,小鼠精子畸变率随着染毒时间的延长和ACN浓度的增高而增高,与对照组比较差异有显著性.结论ACN对男、女生殖系统都有一定的毒作用.

  18. 丙烯腈对小鼠肺成纤维细胞增殖分化的影响%Effect of Acrylonitrile on Proliferation and Differentiation of Mouse Lung Fibroblasts in Vitro

    Institute of Scientific and Technical Information of China (English)

    端礼荣; 吴全义; 张志坚

    2006-01-01

    目的 研究丙烯腈(ACN)对小鼠肺成纤维细胞增殖分化的影响.方法 将ICR小鼠肺成纤维细胞纯化后进行细胞培养,加入二甲亚砜和浓度分别为0.01、0.5、1.0、10.0、50.0、100.0、200.0μg/ml的ACN,作为对照组和染毒组,每组10个平行样.从细胞形态学角度,通过细胞计数,观察细胞生长与分化的过程,同时测定蛋白质含量、丙二醛(MDA)含量和超氧化物歧化酶(SOD)活力.结果 浓度为0.01、0.5、1.0、10.0μg/ml的ACN对小鼠肺成纤维细胞生长无抑制作用,而浓度达到50.0、100.0、200.0μg/ml时,小鼠肺成纤维细胞的增殖和分化明显受到抑制,集落形成率明显减少,细胞体积变小,且随着ACN浓度的加大,其抑制作用增大.当ACN剂量为50.0、100.0、200.0μg/ml时,小鼠肺成纤维细胞相对蛋白质含量低于对照组(P<0.05).当ACN剂量为10.0、50.0、100.0、200.0μg/ml时,小鼠肺成纤维细胞MDA的含量高于对照组(P<0.01).当ACN剂量为10.0、50.0、100.0、200.0μg/ml时,小鼠肺成纤维细胞SOD活力低于对照组(P<0.05).结论 ACN能抑制小鼠肺成纤维细胞增殖和分化,可能与其能抑制蛋白质合成,并引起脂质过氧化有关.

  19. Preparation of Graft Copolymer of Acrylonitrile and Cassava Starch and Its Application in Paper Coating%乳液接枝共聚法改性淀粉的制备及其在涂布纸中的应用

    Institute of Scientific and Technical Information of China (English)

    李楠; 张光华; 刘静

    2008-01-01

    以氧化木薯淀粉为原料,过硫酸钠.亚硫酸氢钠为引发剂,在酸性介质中与单体丙烯腈进行接枝共聚反应,并以此接枝共聚改性淀粉为胶黏剂配制涂料进行涂布,考察了不同的反应单体浓度和木薯淀粉不同的氧化程度下制备的改性淀粉对涂布性能的影响.结果表明,接枝共聚淀粉作为胶黏剂进行纸张涂布后,涂布纸具有理想的表面强度及平滑度.

  20. 丙烯腈-酪素在硫氰酸钠浓溶液中接枝共聚的研究%Study on Graft Copolymerization of Acrylonitrile onto Casein in Concentrated Solution of Sodium Sulfocyanate

    Institute of Scientific and Technical Information of China (English)

    李华雨

    2001-01-01

    丙烯腈、酪素在硫氰酸钠浓水溶液中均相接枝共聚,研究了反应时间、单体质量分数、引发剂质量分数、反应温度对接枝共聚的影响,在共聚反应时间100min,AN 12.8%,Casein 5.4%,AIBN 0.18%,NaSCN 44%,温度72℃时,接枝率为88.4%~91.1%,产率为90.1%~91.1%,接枝效率77.4%~77.5%.

  1. Study on Graft Copolymerization of Acrylonitrile onto Casein in Concentration Aqueous Solution of Sodium Thiocyanate%在硫氰酸钠浓水溶液中丙烯腈-酪素接枝共聚的研究

    Institute of Scientific and Technical Information of China (English)

    董擎之; 唐闻群; 顾利霞

    2000-01-01

    采用傅利叶红外光谱表征了在硫氰酸钠(NaSCN)浓水溶液中丙烯腈(AN)、酪素(Casein)均相接枝共聚制得的接枝共聚主产物为AN-g-Casein接枝共聚物,研究了反应时间、单体质量分数、引发剂质量分数、反应温度对接枝共聚的影响,讨论了反应前酪素的溶解条件.

  2. The investigation of polyethylene surface modification by cold plasma induced grafting polymerization of acrylonitrile%等离子体引发接枝聚合丙烯腈对聚乙烯表面改性的研究

    Institute of Scientific and Technical Information of China (English)

    刘艳璞; 施来顺; 巴换粉; 郭芳

    2009-01-01

    研究了等离子体引发单体接枝聚合对聚合物的表面改性.选取PE为聚合物底材接枝丙烯腈,研究了接枝反应条件对接枝率的影响规律.反应温度愈高,接枝率愈大,当反应温度达到溶液的沸点时,接枝率急剧增大;随着单体浓度的增大,接枝率几乎呈现出线性增长的趋势;接枝率随反应时间的延长而增大.溶剂对接枝反应有较大的影响,当选用(甲醇+水)作为混合溶剂时,接枝率随着水与醇的体积比R(R=V(H_2O)/V(C_nH_(2n+1)OH))的增加而增加.当选用(乙醇+水)或(异丙醇+水)作为混合溶剂时,水醇体积比R为零(即溶剂为纯乙醇或异丙醇时)接枝率最大,当溶剂中有水参与时,接枝率下降.并利用ATR-FTIR分析证明了丙烯腈单体接枝到聚合物薄膜样品表面.

  3. Quick Analysis of Acrylamide and Acrylonitrile by Refraction Method and Timed Gas Chromatography%折射法与定时进样气相色谱法快速测定丙烯酰胺和丙烯腈

    Institute of Scientific and Technical Information of China (English)

    孙旭东; 于慧敏; 史悦; 沈忠耀

    2005-01-01

    为了满足游离细胞催化、多级膜生物反应器连续转化生产丙烯酰胺的新工艺对丙烯酰胺和丙烯腈浓度进行监控的需要,分别提出了采用阿贝折射仪快速分析丙烯酰胺和定时进样气相色谱外标法快速分析丙烯腈浓度的新方法.与传统的丙烯酰胺和丙烯腈的气相色谱内标方法相比,新方法在保持原有气相色谱分析精度的基础上,显著提高了分析的时效性,可以对各级成分变化做准确及时的分析和监控,从而保证了多级膜反应器连续转化过程的操作稳定性.

  4. 丙烯酸偕二硝基丙酯聚合动力学及与丙烯腈的共聚合%Kinetics of 2,2-Dinitropropyl Acrylate Polymerization and the Copolymerization with Acrylonitrile

    Institute of Scientific and Technical Information of China (English)

    张公正; 王芳; 向星

    2010-01-01

    采用膨胀计法研究了丙烯酸偕二硝基丙酯(DNPA)在甲苯溶液中聚合动力学,确定了聚合速率方程,并研究了丙烯酸偕二硝基丙酯与丙烯腈(AN)在甲苯溶液中共聚合的动力学行为,利用红外光谱法测定了共聚物的组成,从而测得了丙烯酸偕二硝基丙酯与丙烯腈的竞聚率.研究结果表明,丙烯酸偕二硝基丙酯聚合速率方程为Rp=k[M]1.18[I]0.60,说明链终止为单基终止和双基终止并存终止方式,引发过程与单体浓度有关;采用Fineman-Ross方法,求得丙烯酸偕二硝基丙酯和丙烯腈两单体的竞聚率分别为γAN=0.508,γDNPA=0.157.

  5. Effect of environmental friendly plasticizer cashew nut shell liquid on properties of acrylonitrile-butadiene rubber%环保型增塑剂腰果壳油对丁腈橡胶性能的影响

    Institute of Scientific and Technical Information of China (English)

    戴洪雁; 陈福林; 岑兰; 周彦豪

    2010-01-01

    研究了腰果壳油(CNSL)用量对丁腈橡胶胶料的硫化特性和硫化胶性能的影响,并与使用邻苯二甲酸二辛酯和环氧大豆油作为增塑剂进行了对比.结果表明,在0~30份(质量)用量内,加入CNSL后胶料的焦烧时间和正硫化时间有所缩短.与加入相同用量的邻苯二甲酸二辛酯和环氧大豆油的胶料及硫化胶相比,使用CNSL的胶料在硫化曲线上的最小转矩和最大转矩以及硫化胶的硬度、定伸应力和耐ASTM 1#标准油体积增加率较小;硫化胶的拉伸强度、撕裂强度、扯断伸长率和耐ASTM 3#标准油体积增加率较大;硫化胶的耐热空气老化性能较好.

  6. Synthesis of Acrylonitrile-butadiene-styrene Copolymer by Styrene-isoprene-butadiene Copolymer Latex%苯乙烯-异戊二烯-丁二烯三元集成胶乳增韧ABS树脂

    Institute of Scientific and Technical Information of China (English)

    尹国强; 李杨; 申凯华; 张峰; 张东梅; 史晶虹; 王玉荣

    2013-01-01

    采用自由基乳液聚合方法,通过苯乙烯-异戊二烯-丁二烯三元共聚合技术,设计合成了新型三元集成胶乳(SIBL)替代传统成本较高的聚丁二烯胶乳(PBL),制备丙烯腈-丁二烯-苯乙烯共聚物(ABS树脂).将高温乳液法制备的SIBL进行附聚,再经过乳液接枝法制备高胶含量的ABS粉料,最后将ABS粉料与本体苯乙烯-丙烯腈共聚物(SAN树脂)掺混、熔融挤出、造粒,制备了低成本新型ABS树脂.考察3种单体配比对SIBL聚合动力学和粒径大小、分布、凝胶含量、玻璃化转变温度(Tg)和ABS树脂性能的影响.结果表明,采用自由基乳液聚合制备三元集成胶乳的方法可行,得到的增韧ABS树脂综合性能优异,悬臂梁缺口冲击强度由139 J/m提高到233 J/m.

  7. Carbon Fibers: Reexamination of the Critical Low-Temperature (200-300C) Stabilization of Polyacrylonitrile,

    Science.gov (United States)

    CARBON FIBERS , SYNTHESIS(CHEMISTRY)), (*ACRYLONITRILE POLYMERS, CARBON FIBERS ), SHEETS, CARBON, FILMS, OXIDATION, THERMAL ANALYSIS, CHEMICAL BONDS, INFRARED SPECTRA, MOLECULAR STRUCTURE, HEAT TREATMENT

  8. 40 CFR 63.11398 - What definitions apply to this subpart?

    Science.gov (United States)

    2010-07-01

    ... acrylonitrile units but less than 85 percent by weight of acrylonitrile units. Monomer recovery process..., monomer vacuum pump flush drum, and drum filter vacuum pump flush drum. Polymerization process equipment... atmosphere (or point of entry into a control device, if any) of a gas stream from the acrylic and...

  9. Compatibilization of blends of low density polyethylene and poly(vinyl chloride) by segmented EB(SAN-block-EB)n block copolymers

    NARCIS (Netherlands)

    Kroeze, E.; Brinke, G. ten; Hadziioannou, G.

    1997-01-01

    Hydrogenated segmented poly[butadiene-block-((styrene-co-acrylonitrile)-block-butadiene)n] block copolymers, which were developed by use of the polymeric iniferter technique, were tested for their compatibilizing capacities for (10/90) LDPE/PVC blends. The acrylonitrile content of the SAN blocks of

  10. Compatibilization of blends of low density polyethylene and poly(vinyl chloride) by segmented EB(SAN-block-EB)(n) block copolymers

    NARCIS (Netherlands)

    Kroeze, E; ten Brinke, G.; Hadziioannou, G

    1997-01-01

    Hydrogenated segmented poly[butadiene-block-((styrene-co-acrylonitrile)-block-butadiene)(n)] block copolymers, which were developed by use of the polymeric iniferter technique, were tested for their compatibilizing capacities for (10/90) LDPE/PVC blends. The acrylonitrile content of the SAN blocks o

  11. Synthesis of SAN-PB-SAN triblock copolymers via a ''living'' copolymerization with macro-photoiniferters

    NARCIS (Netherlands)

    Kroeze, E; de Boer, B.; ten Brinke, G.; Hadziioannou, G

    1996-01-01

    A technique is described for the synthesis of poly((styrene-co-acrylonitrile)-block-butadiene-block-(styrene-co-acrylonitrile)) (SAN-PB-SAN) triblock copolymers through polybutadiene-based photo-iniferters. Dihydroxy- and dicarboxy-terminated polybutadienes were transformed into the chloro-terminate

  12. 77 FR 67726 - Department of State: State Department Sanctions Information and Guidance

    Science.gov (United States)

    2012-11-13

    ... potentially sanctionable. ``Petrochemical products'' includes any aromatic, olefin, and synthesis gas, and any of their derivatives, including ethylene, propylene, butadiene, benzene, toluene, xylene, ammonia..., acrylonitrile butadiene styrene, alachlor, ammonium nitrate, ammonium sulfate, anhydrous ammonia,...

  13. MW-assisted synthesis of carboxymethyl tamarind kernel polysaccharide-g-polyacrylonitrile: optimization and characterization.

    Science.gov (United States)

    Meenkashi; Ahuja, Munish; Verma, Purnima

    2014-11-26

    Microwave-assisted synthesis of graft copolymer of carboxymethyl tamarind seed polysaccharide and polyacrylonitrile was carried out. The effect of formulation and process variables on grafting efficiency of carboxymethyl tamarind kernel polysaccharide-g-poly(acrylonitrile) was studied using response surface methodology. The results revealed that the significant factors affecting grafting efficiency were concentrations of ammonium persulphate, acrylonitrile and interaction effects of ammonium persulphate and acrylonitrile concentrations. The optimal calculated parameters were found to be microwave exposure time-99.48 s, microwave exposure power-160 W, concentration of acrylonitrile-0.10% (w/v), concentration of ammonium persulphate--40 mmol/l, which provided graft copolymer with grafting efficiency of 96%. The formation of graft copolymer was confirmed by FT-IR studies and validated by scanning electron micrographs. Thermogravimetric analysis indicated higher thermal stability of graft copolymer and X-ray diffraction study revealed increase in crystallinity on graft polymerization. Further, the graft copolymer showed pH dependant swelling.

  14. Recycling of engineering plastics from waste electrical and electronic equipments: influence of virgin polycarbonate and impact modifier on the final performance of blends.

    Science.gov (United States)

    Ramesh, V; Biswal, Manoranjan; Mohanty, Smita; Nayak, Sanjay K

    2014-05-01

    This study is focused on the recovery and recycling of plastics waste, primarily polycarbonate, poly(acrylonitrile-butadiene-styrene) and high impact polystyrene, from end-of-life waste electrical and electronic equipments. Recycling of used polycarbonate, acrylonitrile-butadiene-styrene, polycarbonate/acrylonitrile-butadiene-styrene and acrylonitrile-butadiene-styrene/high impact polystrene material was carried out using material recycling through a melt blending process. An optimized blend composition was formulated to achieve desired properties from different plastics present in the waste electrical and electronic equipments. The toughness of blended plastics was improved with the addition of 10 wt% of virgin polycarbonate and impact modifier (ethylene-acrylic ester-glycidyl methacrylate). The mechanical, thermal, dynamic-mechanical and morphological properties of recycled blend were investigated. Improved properties of blended plastics indicate better miscibility in the presence of a compatibilizer suitable for high-end application.

  15. Synthesis and E/Z Configuration Determination of Novel Derivatives of 3-Aryl-2-(benzothiazol-2'-ylthio Acrylonitrile, 3-(Benzothiazol-2'-ylthio-4-(furan-2''-yl-3-buten-2-one and 2-(1-(Furan-2''-yl-3'-oxobut-1''-en-2-ylthio-3-phenylquinazolin-4(3H-one

    Directory of Open Access Journals (Sweden)

    Adel Abou El-Khair

    2011-07-01

    Full Text Available Knoevenagel condensation of 2-(benzothiazol-2-ylthio acetonitrile (2 with either furan-2-carbaldehyde or thiophene-2-carbaldehydes leads to E-isomers 4a–b exclusively, while the condensation of the compound 2 with benzaldehyde or para-substituted benzaldehydes with an electron-donating group afforded E/Z mixtures 4c–e with preferentially formation of the E-isomer. Condensation of furan-2-carbaldehyde (3a with either 1-(benzothiazol-2'-ylthio propan-2-one (5 or 2-(2'-oxo propylthio-3-phenyl-quinazolin-4(3H-one (9 leads exclusively to the Z-isomers of 6 and 10, respectively. The structures of the newly synthesized compounds were elucidated by elemental analyses, 1H-NMR and 13C-NMR spectra, COSY, HSQC, HMBC, NOE, MS and X-ray crystallographic investigations.

  16. 丙烯腈对中国仓鼠肺细胞细胞活力和间隙连接通讯功能的影响%The effects of acrylonitrile on viability and gap junctional intercellular communication in CHL cells

    Institute of Scientific and Technical Information of China (English)

    张正东; 金复生; 朱瑞娟; 范卫; 金锡鹏

    2001-01-01

    目的探讨丙烯腈(ACN)对中国仓鼠肺细胞(CHL)细胞活力及细胞间隙连接通讯(GJIC)功能的影响.方法镜下观察细胞形态学改变,采用MTT法测定细胞生长半数抑制浓度(IC50),应用荧光染料示踪技术观测ACN对CHL细胞GJIC的影响.结果 ACN染毒12和24 h,细胞生长IC50分别为435.73和251.09 μg/ml.低剂量组(12.5和25.0 μg/ml)细胞形态与对照组相比无明显改变,较高剂量组(50.0~200.0 μg/ml)细胞轻度受损(0~Ⅰ级),高剂量组(800.0 μg/ml)细胞明显受损(Ⅲ级).ACN原形在无明显细胞毒性剂量(10.0~50.0 μg/ml)时即可抑制GJIC,并呈持续抑制作用,存在剂量-效应和时间-效应关系.ACN经代谢活化后,可加重对细胞GJIC的抑制作用和细胞受损程度,但在染毒12 h后停止接触,该作用在一定程度上可逆转.牛磺酸作为一种重要的抗氧化剂,预处理细胞(牛磺酸剂量为10和20 mmol/L)可明显抑制ACN对细胞GJIC的下调作用.结论 ACN在较高剂量时对CHL细胞具有毒性作用,但在无明显细胞损伤剂量时即能明显抑制细胞GJIC功能,该抑制作用在停止接触ACN或有抗氧化剂存在时可逆转,提示氧化应激在ACN所致细胞GJIC功能下调中具有重要作用.

  17. Effect of acrylonitrile on proliferation and differentiation of rat embryo spinal cord nerve cells in vitro%丙烯腈对体外培养大鼠胚胎脊髓神经细胞增殖分化的影响

    Institute of Scientific and Technical Information of China (English)

    端礼荣; 吴全义; 陆荣柱

    2005-01-01

    目的研究丙烯腈(ACN)对体外培养的大鼠胚胎脊髓神经细胞增殖分化的影响.方法 16 d的大鼠胚胎脊髓组织作原代细胞培养,从细胞形态学及细胞计数观察研究细胞生长与分化过程,同时测定蛋白质含量和丙二醛(MDA)含量并与对照组进行比较.结果 10.0~100.0 mg/L ACN组明显抑制脊髓神经细胞分化、增殖、集落形成率明显减少,细胞体积小,细胞内MDA含量增加,蛋白质相对含量降低,并显示浓度效应关系.结论 ACN引起的大鼠胚胎脊髓神经细胞的增殖和分化抑制,可能与ACN诱发蛋白质合成下降和脂质过氧化物有关.

  18. pH响应型聚丙烯腈-丙烯酰胺-丙烯酸多孔水凝胶的制备及其在环境污染方面的应用%Preparation of pH sensitive poly(acrylonitrile-acrylamide-acrylic acid) hydrogel and its application in enviromental pollution

    Institute of Scientific and Technical Information of China (English)

    李宪华; 郭永存; 朱涛

    2013-01-01

    Pb2+离子是一种重要的污染源,因此有效的移走不仅是对环境更是对人类健康具有重要意义.我们利用pH响应型聚丙烯腈-丙烯酰胺-丙烯酸多孔水凝胶作为吸附剂来移走Pb2+离子.探讨了时间、pH和温度对吸附能力的影响.结果表明在pH为5,温度为25℃时,有最大的吸附能力,达到了1.578mg.更为有趣的是可以通过改变pH来改变聚合物链相变的办法实现水凝胶的重复利用.

  19. 聚(丙烯腈-对羟基苯乙烯)与聚碳酸酯及聚四甲基双酚-A碳酸酯的相容性研究%MISCIBILITY OF POLY( ACRYLONITRILE-co-4-VINYLPHENOL) WITH BISPHENOL-A POLYCARBONATE AND TETRAMETHYL BISPHENOL-A POLYCARBONATE

    Institute of Scientific and Technical Information of China (English)

    孟诗云; 姜苏俊; 李光宪

    2004-01-01

    在聚(丙烯腈-苯乙烯)[P(S-AN)]中苯乙烯(S)苯环的对位引入羟基基团获得聚(丙烯腈-对羟基苯乙烯)[P(AN-VPh)],P(AN-VPh)与聚碳酸酯(PC)体系及P(AN-VPh)与聚四甲基双酚-A碳酸酯(TMPC)体系的相容性实验结果表明,由于对羟基苯乙烯(VPh)的引入,使体系中同时存在"分子间特殊相互作用"和"分子内排斥性相互作用"两种效应,从而使体系的相容性获得改善.P(AN-VPh)共聚物中AN的摩尔百分含量在12.3%~49.5%范围内时,P(AN-VPh)/PC共混物体系为热力学均相体系,采用TMPC替代PC与P(AN-VPh)共混时,共聚物中AN的摩尔百分含量在0~58.9 mol%范围内TMPC/P(AN-VPh)共混物体系为热力学相容体系.通过Flory-Huggins平均场理论计算与拟合所获得的相容窗口相图与实验值较为吻合,同时获得相互作用参数TMPC-VPh=-0.19.

  20. Preparation and Properties of Epoxidized Acrylonitrile-butadiene rubber/Carboxylic Carbon Nanotubes Composites%环氧化丁腈橡胶/羧基化碳纳米管复合材料的制备与性能研究

    Institute of Scientific and Technical Information of China (English)

    徐绍彬; 任文坛; 张勇; 张隐西

    2010-01-01

    采用无溶剂反应性加工技术,以叔丁基过氧化氢为氧化剂、三氧化钼为催化剂,在哈克转矩流变仪中实施了原位催化环氧化反应.产物的全反射红外光谱证实了环氧化丁腈橡胶的生成,用化学滴定法测定了其环氧化度为3.6%;将环氧化丁腈橡胶与羧基化多壁碳纳米管(MWNT-COOH)直接共混制备复合材料,研究了MWNT-COOH对复合材料的硫化性能、动态力学性能、热性能的影响.结果表明,复合材料在150℃~190℃范围内表现出较好的硫化性能,MWNT-COOH含量提高可促进橡胶的交联;复合材料在温度低于Tg时,MWNT-COOH可显著提高材料的储能模量;复合材料的热稳定性能随MWNT-COOH用量的增加而提高,其中4份用量的MWNT-COOH可使环氧化丁腈橡胶的最大热失重速率温度由465℃提高到471℃.

  1. 2-氰基-3-(6-氯-3-吡啶甲基)胺基-3-脂肪胺基丙烯腈的合成与生物活性%Synthesis and Biological Activities of 2-Cyano-3-(6-Chloro-3-Pyridylmethyl)Amino-3-Aliphatic Amine Acrylonitrile

    Institute of Scientific and Technical Information of China (English)

    余申义; 李正名

    2001-01-01

    以3-氨甲基吡啶和2-氯-5-氨甲基吡啶为原料先与2-氰基-3,3-二甲硫基丙烯腈反应,产物不经分离再与脂肪胺反应合成了14个未见文献报道的开环类吡虫啉结构类似物.所有目标化合物均经元素分析、1H NMR确证.初步活性测试结果表明含硫化合物的杀虫活性优于双氨基化合物,其中4c对豆蚜的抑制率最高达87.6%.

  2. Effects of acrylonitrile on T lymphocytes' the lipid raft protein Caveolin-1 and the MEK protein in vitro%丙烯腈T淋巴细胞体外染毒对其脂筏Caveolin-1蛋白、MEK蛋白的影响

    Institute of Scientific and Technical Information of China (English)

    李秀菊; 黄简抒; 王朋; 周元陵; 范卫

    2013-01-01

    目的 丙烯腈染毒T淋巴细胞,分析膜脂筏及Ras/Raf/MEK/ERK信号通路中MEK蛋白变化,探讨丙烯腈免疫毒性的可能作用机制.方法 采取体外细胞培养技术,以T淋巴细胞Jurkat细胞株为研究对象,分为空白对照组、低浓度、中浓度、高浓度丙烯腈(0、20、100和500μmol/l)细胞染毒组,分析膜脂筏Caveolin-1蛋白、MEK蛋白变化.结果 随染毒浓度增加,受检细胞经处理4h后各染毒组与对照组细胞膜胆固醇含量差异有统计学意义(P<0.05),细胞膜胆固醇的含量下降,间接表明脂筏的数量越少;Caveolin-1蛋白定位改变,变构便于信号传递;p-MEK蛋白随浓度增高条带变浅.结论 丙烯腈可能通过破坏脂筏结构,脂筏数量减少,Caveolin-1蛋白位移变构,Ras/Raf/MEK/ERK信号传导过程受到抑制而发挥免疫毒性.

  3. Preparation and properties of adjacency crosslinked hydroxyl-terminated liquid butadiene-acrylonitrile rubber based polyurethane elastomers%邻接交联型端羟基液体丁腈橡胶基聚氨酯弹性体的制备与性能

    Institute of Scientific and Technical Information of China (English)

    董慧民; 张成龙; 彭汉修; 李再峰

    2011-01-01

    The styrene-butadiene rubber ( SBR ) / boehmite( BM) composites were prepared by directly blending. The effects of BM content and its surface modification with silane coupling agent bis-[γ-( trie-thoxysilyl) -propyl ] -tetrasulfide (Si 69 ) on mechanical properties, micro morphology, curing characteristics and dynamic mechanical properties of the composites were investigated. The results showed that BM could improve the mechanical properties of SBR vulcanizates effectively. The mechanical properties and interfacial bonding of SBR/BM composites could be further improved when BM was treated with Si 69. The scorching time and optimum curing timeof the two kinds of composites were shortened with increasing BM content at lower BM loading. Compared with the SBR/silica composites, SBR/BM composites exhibited higher mechanical loss in the low temperature range ( -20-0℃ ) and the SBR/ Si 69 modified BM exhibited lower mechanical loss in the high temperature range (50-70℃) when the filler content was the same.%以端羟基液体丁腈橡胶、二苯基甲烷二异氰酸酯及扩链剂1,4 -丁二醇为原料,加入自由基引发剂2,5-二甲基-2,5-双(过氧化叔丁基)己烷和交联助剂三烯丙基异三聚氰酸酯( TAIC),制备了邻接交联型聚氨酯弹性体(PUE),考察了 TAIC的用量对PUE力学性能的影响,并对PUE的热性能进行了研究.结果表明,随着TA IC用量的增加,PUE的交联密度增大,分子柔顺性降低,材料的力学性能逐渐提高,耐热性增强,玻璃化转变温度升高.

  4. Determination of Reactivity Ratio of Free Radical Copolymerization of Macrocyclic Monoazacrown Ether and Acrylonitrile and Study on Its Copolymer Thermoproperty%大环单氮杂冠醚与丙烯腈的自由基共聚反应竞聚率的测定及其共聚物的热力学性质研究

    Institute of Scientific and Technical Information of China (English)

    侯瑞斌; 陈铁; 金龙一

    2008-01-01

    利用Fineman-Ross方法,在甲苯溶剂中测定了大环N-(4-乙烯基苄基)-1-单氮杂-m-亚苯基-34-冠-11单体与丙烯腈的共聚合反应的单体竞聚率,其值分别为3.99和0.19,并采用TGA和DSC简略地研究了共聚物的热力学性质.

  5. 纳米氧化镁对甲基丙烯酸-丙烯腈共聚体系竞聚率的影响%Impact of nano-sized magnesium oxide on the reactivity ratios of methacrylic acid-acrylonitrile copolymerization system

    Institute of Scientific and Technical Information of China (English)

    贺海龙; 李玲

    2013-01-01

      要: 以偶氮二异丁腈(AIBN)为引发剂,引发甲基丙烯酸(MAA)和丙烯腈(AN)本体聚合.采用滴定法和称重法测定了在低转化率(小于10%)下不同单体配比的共聚物组成,并采用Fineman-Ross法及Kelen-Tudos法计算、作图得到两种单体的竞聚率,它们的最大差值为0.09,说明滴定法和称重法具有一定的可信度.用上述方法测定了反应体系在纳米MgO存在下共聚单体竞聚率的变化,结果表明:加入纳米MgO,MAA和AN的竞聚率均下降.%The copolymer of methacrylic acid (MAA) and acrylonitrile (AN) was synthesized by using azobisisobutyronitrile (AIBN) as initiator via bulk polymerization. The composition of the copolymer with mono-mers in different ratios were determined by titration and gravimetric method at a low conversion rate (less than 10%), and the reactivity ratios of the two monomers were calculated with Fineman-Ross (FR) and Kelen-Tudos (KT) method. The maximum difference in reactivity ratio between FR and KT method was 0.09, indicat-ing that titration and gravimetric method both had certain credibility. The changes of the reactivity ratios of the monomers were determined with the mentioned methods in the presence of nano-sized magnesium oxide in the system. The results showed that nano-sized magnesium oxide made both of the two monomers′ reactivity ratios decline.

  6. 丙烯腈-丙烯酸共聚物超细纤维的制备及其pH响应性能的研究%Preparation and pH-responsive properties of poly (acrylonitrile-co-acrylic acid) ultrafine fibers

    Institute of Scientific and Technical Information of China (English)

    王兵; 林义; 彭锦荣; 李瑞霞; 吴大诚

    2010-01-01

    以N,N-二甲基甲酰胺(DMF)为溶剂,通过气流-静电纺丝法制备了具有pH响应性能的丙烯腈-丙烯酸共聚物(Poly(AN-co-AA))超细纤维.利用扫描电镜(SEM)对超细纤维形貌进行表征,研究了聚合单体中丙烯酸(AA)的含量、纺丝溶液中L-苯丙氨酸 (L-Phe)的含量和浸泡时间对Poly(AN-co-AA)超细纤维形貌的影响,并从缓冲溶液的pH值及其与纤维直径变化的可逆性等方面研究了Poly(AN-co-AA)超细纤维的pH响应性能,确定了制备具有pH响应性能的Poly(AN-co-AA)超细纤维的最佳工艺参数.

  7. Composite Materials Handbook. Volume 1. Polymer Matrix Composites Guidelines for Characterization of Structural Materials

    Science.gov (United States)

    2007-11-02

    Carbon Fibers -- Fibers produced by the pyrolysis of organic precursor fibers such as rayon, poly- acrylonitrile (PAN), and pitch in an inert atmosphere...derived from the controlled pyrolysis of poly(acrylonitrile) fiber. Parallel Laminate -- A laminate of woven fabric in which the plies are aligned in...content and void content. At a given void content, laminate fiber volume fraction is en- tirely dependent upon resin content. Furthermore, for a given

  8. Jet Engine Exhaust Analysis by Subtractive Chromatography

    Science.gov (United States)

    1978-12-01

    and J. J. Brooks. Development of a portable miniature collection system for the exposure as- sessment within the microenvironment for carcinogens ...65 A-2. Recovery of acrylonitrile from standard sample generation system ...... ............. 66 B-I. Jet engine exhaust sampling and analysis...7 n-Butane 0.16 2.6 minutes 8 Propylene oxide 3.14 52 minutes 9 Acrylonitrile 9.35 2.6 hours 10 Phenanthrene 1.9 x 106 61 years 11 4-Bromodiphenyl

  9. 丙烯腈对大鼠脑组织和神经胶质细胞中核因子-kB信号传导通路活性及相关基因表达的影响%Effects of acrylonitrile on the activation of nuclear factor-kB signaling pathways and related gene expression in rat brain and rat glial cells

    Institute of Scientific and Technical Information of China (English)

    焦振泉; 裴晓燕; 郭云昌; 徐勇

    2008-01-01

    目的 丙烯腈(ACN)对大鼠脑组织和大鼠神经胶质细胞中核因子KB(NF-kB)信号传导通路活性及相关基因表达的影响.方法 利用micorarray和EMSA实验测定了SD大鼠经0和200mg/kg ACN分别作用14、28和90天后,大鼠脑组织NF-kB信号传导通路活性的变化及相关基因表达的变化;大鼠神经胶质细胞经0、25、50和75μg/ml ACN作用4和24h后细胞NF-kB信号传导通路活性的变化及相关基因表达的变化.结果 ACN促进大鼠脑组织(体内)和神经胶质细胞(体外)NF-kB信号传导通路相关基因(NIK、IKK、NF-kB1、NF-KB2、IkBa和c-myc)的表达.EMSA实验也进一步证实了ACN可激活大鼠脑组织和大鼠神经胶质细胞中NF-kB信号传导通路.结论 ACN诱导的氧化应激和ACN激活NF-kB信号传导通路具有一定的关系.

  10. (Z-3-(1-Benzofuran-2-yl-2-(3,4,5-trimethoxyphenylacrylonitrile

    Directory of Open Access Journals (Sweden)

    Sean Parkin

    2012-03-01

    Full Text Available In the title compound, C20H17NO4, the double bond of the acrylonitrile group separating the 1-benzofuran moiety from the 3,4,5-trimethoxyphenyl ring has Z geometry. The 1-benzofuran groups are π–π stacked with inversion-related counterparts such that the furan ring centroid–centroid distance is 3.804 (5 Å. The dihedral angle between the planes of the trimethoxyphenyl ring and the acrylonitrile group is 24.2 (2°.

  11. Effect of heating rate on toxicity of pyrolysis gases from some elastomers

    Science.gov (United States)

    Hilado, C. J.; Kosola, K. L.; Solis, A. N.

    1977-01-01

    The effect of heating rate on the toxicity of the pyrolysis gases from six elastomers was investigated, using a screening test method. The elastomers were polyisoprene (natural rubber), styrene-butadiene rubber (SBR), ethylene propylene diene terpolymer (EPDM), acrylonitrile rubber, chlorosulfonated polyethylene rubber, and polychloroprene. The rising temperature and fixed temperature programs produced exactly the same rank order of materials based on time to death. Acrylonitrile rubber exhibited the greatest toxicity under these test conditions, and carbon monoxide was not found in sufficient concentrations to be the primary cause of death.

  12. Electrically Conducting Polymer-Copper Sulphide Composite Films, Preparation by Treatment of Polymer-Copper (2) Acetate Composites with Hydrogen Sulfide

    Science.gov (United States)

    Yamamoto, Takakazu; Kamigaki, Takahira; Kubota, Etsuo

    1988-01-01

    Polymer copper sulfide composite films were prepared by treatment of polymer poly(vinyl chloride), poly(acrylonitrile), copolymer of vinyl chloride and vinyl acetate (90:10), and ABS resin copper (2) acetate composites with hydrogen sulfide. The films showed electrical conductivity higher than 0.015 S/cm when they contained more than 20 wt percent of copper sulfide. A poly(acrylonitrile)-copper sulfide composite film containing 40 to 50 wt percent of copper sulfide showed electrical conductivity of 10 to 150.0 S/cm and had relatively high mechanical strength to be used in practical purposes.

  13. Regioselective Synthesis of Some Pyrazole Scaffolds Attached to Benzothiazole and Benzimidazole Moieties

    Directory of Open Access Journals (Sweden)

    Nabila A. Kheder

    2014-01-01

    Full Text Available Condensation of 2-(benzothiazol-2-ylacetonitrile (1 or 2-(1-methyl-1H-benzimidazol-2-ylacetonitrile (2 with thiophene-2-carbaldehyde afforded the corresponding acrylonitrile derivatives 3 or 4, respectively. The 1,3-dipolar cycloaddition reaction of the acrylonitrile 3 or 4 with nitrile-imine 6 gave novel pyrazole derivatives pendant to benzothiazole and benzimidazole. The pyrazoline derivative 7 was converted into the corresponding pyrazole derivative 11 via thermal elimination of hydrogen cyanide upon heating in sodium ethoxide solution. The structures of the synthesized products were confirmed by IR, 1H NMR, and mass spectral techniques.

  14. Simple 3D Printed Scaffold-Removal Method for the Fabrication of Intricate Microfl uidic Devices

    NARCIS (Netherlands)

    Saggiomo, V.; Velders, A.H.

    2015-01-01

    An easy and cheap fabrication method for intricate polydimethylsiloxane microfluidic devices is presented. The acrylonitrile butadiene styrene scaffold-removal method uses cheap, off-the-shelf materials and equipment for the fabrication of intricate microfluidic devices. The versatility of the metho

  15. Inducing Expression and Reaction Characteristic of Nitrile Hydratase from Rhodococcus sp. SHZ-1%Rhodococcus sp.SHZ-1腈水合酶的诱导表达和稳定性研究

    Institute of Scientific and Technical Information of China (English)

    王超; 张根林; 徐小琳; 李春

    2007-01-01

    Inducing expression and the reaction characteristic of nitrile hydratase (NHase) from Rhodococcus sp.SHZ-1 were investigated. The results showed that the expression of NHase was greatly enhanced with the cooperation of acrylonitrile and ammonium chloride as inducer in the medium and the specific activity of NHase was increased of 44%. Then the temperature, pH, concentration of acrylonitrile and acrylamide were evaluated, which affected the activity and reaction characteristic of NHase. It was found that the temperature and concentration of acrylamide were the most important factors for the catalyzation of NHase. The optimal catalysis temperature of NHase from Rhodococcus sp. SHZ-1 was 30℃, and the activation energy of the hydration of NHase was 90.2kJ·mol-1 in the temperature range from 5℃ to 30℃. Km of NHase was 0.095mol.L-1 using acrylonitrile(AN)as substrate, and NHase activity was inhibited seriously when acrylonitrile concentration was up to 40g·L-1, the substrate inhibition constant Ki is 0.283mol·L-1. Moreover, the NHase from Rhodococcus sp. SHZ-1 had very strong tolerance to acrylamide, in which the final concentration of acrylamide reached to 642g·L-1 and the residual activity of NHase still maintained 8.6% of the initial enzyme activity.

  16. Selective Oxidative Decarboxylation of Amino Acids to Produce Industrially Relevant Nitriles by Vanadium Chloroperoxidase

    NARCIS (Netherlands)

    But, A.; Notre, le J.E.L.; Scott, E.L.; Wever, R.; Sanders, J.P.M.

    2012-01-01

    Industrial nitriles from biomass: Vanadium-chloroperoxidase is successfully used to transform selectively glutamic acid into 3-cyanopropanoic acid, a key intermediate for the synthesis of bio-succinonitrile and bio-acrylonitrile, by using a catalytic amount of a halide salt. This clean oxidative dec

  17. Insight into the transport of hexane-solute systems through tailor-made composite membranes

    NARCIS (Netherlands)

    Stafie, N.; Stamatialis, D.F.; Wessling, M.

    2004-01-01

    This work presents composite membranes comprising poly(acrylonitrile) (PAN) as the support and polydimethylsiloxane (PDMS) as the selective top layer. For sunflower oil/hexane and polyisobutylene (PIB)/hexane, the permeation characteristics of these membranes for various feed concentrations and pres

  18. Exceptionally large banded spherulites

    Science.gov (United States)

    Lagasse, R. R.

    1994-07-01

    This article concerns the crystallization of maleic anhydride from a blend containing 2 wt% of poly(acrylonitrile). High speed photography and temperature measurements during the crystallization as well as X-ray diffraction from the blend after crystallization are consistent with a banded spherulitic morphology.

  19. Fast ethylamine gas sensing based on intermolecular charge-transfer complexation

    Institute of Scientific and Technical Information of China (English)

    Eun Mi Lee; Seon Young Gwon; Young A Son; Sung Hoon Kim

    2012-01-01

    We have investigated the fast ethylamine gas sensing of 2-chloro-3,5-dinitrobenzotrifluoride (CDBF) loaded poly(acrylonitrile)nanofiber based on an intermolecular charge-transfer complexation.Reversible response and recovery were achieved using alternating gas exposure.This system shows a fast ethylamine gas sensing within 0.4 s.

  20. A method for the production of weakly acidic cation exchange resins

    Science.gov (United States)

    Heller, H.; Werner, F.; Mitschker, A.; Diehl, H. V.; Schaefer, A.

    1991-12-01

    The invention relates to a nonpolluting method for the production of weakly acidic cation exchange resins by saponification of cross-linked acrylonitrile bead polymers, with an alkaline saponification agent at elevated temperature, according to which method the bead polymer and alkaline saponification agent are jointly added only at elevated temperature.

  1. Morita–Baylis–Hillman reaction of acrylamide with isatin derivatives

    Directory of Open Access Journals (Sweden)

    Radhey M. Singh

    2014-12-01

    Full Text Available The Morita–Baylis–Hillman reaction of acrylamide, as an activated alkene, has seen little development due to its low reactivity. We have developed the reaction using isatin derivatives with acrylamide, DABCO as a promoter and phenol as an additive in acetonitrile. The corresponding aza version with acrylate and acrylonitrile has also been developed resulting in high product yields.

  2. Syntheses and Surface Properties of Polyacrylonitrile-based Copolymer Membranes Containing Sugar Moieties

    Institute of Scientific and Technical Information of China (English)

    HUANG Xiao-jun; WAN Ling-shu; DAI Zheng-wei; KOU Rui-qiang; XU Zhi-kang

    2005-01-01

    To improve the hydrophilicity of polyacrylonitrile-based membranes, sugar moieties were incorporated into acrylonitrile-based copolymers via the radical copolymerization of α-allyl glucoside(AG) with acrylonitrile(AN) with 2,2'-azobis-iso-butyronitrile(AIBN) as the initiator in dimethyl sulphoxide(DMSO). It was found that the yield increased with the increase of the initiator concentration and reaction time, while it decreased with the increase of the monomer molar ratio of AG to AN. Raising the AG proportion in the monomer mixture resulted in the increase of the AG content in the copolymer. Mv of the copolymers decreased with increasing the AG monomer fraction in feed. The copolymers were fabricated into dense membranes and their surface properties were studied by means of the water contact angle measurement and platelet adhesion tests. It was found that the static water contact angle on the membrane decreased significantly from 70° to 33° with the increase of the AG content. The adhesive number of platelets on the membrane surface also decreased significantly with increasing AG content in the copolymers. These results demonstrate that the hydrophilicity and biocompatibility of the acrylonitrile-based copolymer membranes could be improved efficiently by the copolymerization of acrylonitrile with vinyl carbohydrates.

  3. 铸造技术

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    A new polymer electrolyte poly(acrylonitrile)-dimethylsulphoxide-salt for electrochemical capacitors,A study ofyttria stabilized zirconia sheets fabricated,An investigation on fine-grain formation and structuralcharacter in cast IN718 superalloy,Automobile components made of magncsium-aluminium composites.

  4. Powder diffraction in structural characterization of dienediaminoketones of the indolin-3-one series

    Indian Academy of Sciences (India)

    Vladimir V Chernyshev; Natalia S Monakhova

    2010-09-01

    Crystal structures of five derivatives of dienediaminoketones - 3-amino-3-(dimethylamino)-2-[(3-oxo-1,3-dihydro-2H-indol-2-ylidene)methyl]acrylonitrile (1); 3-amino-2-[(3-oxo-1,3-dihydro-2Hindol-2-ylidene)methyl]-3-pyperidin-1-ylacrylonitrile (2); 3-amino-3-morpholin-4-yl-2-[(3-oxo-1,3-dihydro-2H-indol-2-ylidene)methyl]acrylonitrile (3); 3-amino-3-[(4-methoxyphenyl)amino]-2-[(3-oxo-1,3-dihydro-2H-indol-2-ylidene)methyl]acrylonitrile (4) and 3-amino-3-(benzylamino)-2-[(3-oxo-1,3-dihydro-2H-indol-2-ylidene)methyl]acrylonitrile (5) - were determined from powder patterns measured with the laboratory powder diffractometer. The single crystal structure of the hydrate of ethanol solvate of 3 - 3·0.33C2H6O·0.33H2O (3a) - is also presented. The hydrogen-bonding patterns of all compounds are discussed.

  5. NBR Demand Up

    Institute of Scientific and Technical Information of China (English)

    Wang Yuying

    2007-01-01

    @@ 1 Output decreased in 2006 By the end of 2006 the capacity of to make NBR (acrylonitrile-butadiene rubber) in China was still maintained at 49.5 thousand t/a, but the output was only 35 thousand tons in 2006, a drop of 9.9% from 2005.

  6. Acrylamide synthesis using agar entrapped cells of Rhodococcus rhodochrous PA-34 in a partitioned fed batch reactor.

    Science.gov (United States)

    Raj, Jog; Sharma, Nitya Nand; Prasad, Shreenath; Bhalla, Tek Chand

    2008-01-01

    The nitrile hydratase (Nhase) induced cells of Rhodococcus rhodochrous PA-34 catalyzed the conversion of acrylonitrile to acrylamide. The cells of R. rhodochrous PA-34 immobilized in 2% (w/v) agar (1.76 mg dcw/ml agar matrix) exhibited maximum Nhase activity (8.25 U/mg dcw) for conversion of acrylonitrile to acrylamide at 10 degrees C in the reaction mixture containing 0.1 M potassium phosphate buffer (pH 7.5), 8% (w/v) acrylonitrile and immobilized cells equivalent to 1.12 mg dcw (dry cell weight) per ml. In a partitioned fed batch reaction at 10 degrees C, using 1.12 g dcw immobilized cells in a final volume of 1 l, a total of 372 g of acrylonitrile was completely hydrated to acrylamide (498 g) in 24 h. From the above reaction mixture 87% acrylamide (432 g) was recovered through crystallization at 4 degrees C. By recycling the immobilized biocatalyst (six times), a total of 2,115 g acrylamide was produced.

  7. Biomarker of Exposure and Mechanism of Action of Toxic Industrial Chemicals (TICs)

    Science.gov (United States)

    2013-07-01

    primary chemicals used, 10 employee 37 samples with a rank of 1 and 10 with a rank of 6. In addition, since AN is a constituent of tobacco smoke and...is/are at least partly responsible for the toxicity and perhaps carcinogenicity of acrylonitrile. Using proteomic approaches we identified 385

  8. Determination of Selected Volatiles in Cigarette Mainstream Smoke. The CORESTA 2009 Collaborative Study and Recommended Method

    Directory of Open Access Journals (Sweden)

    Intorp M

    2014-12-01

    Full Text Available A recommended method has been developed and published by CORESTA, applicable to the quantification of selected volatiles (1,3-butadiene, isoprene, acrylonitrile, benzene, and toluene in the gas phase of cigarette mainstream smoke. The method involved smoke collection in impinger traps and detection and measurement using gas chromatography/mass spectrometry techniques.

  9. A column-switching liquid chromatography-tandem mass spectrometry method for quantitation of 2-cyanoethylmercapturic acid and 2-hydroxyethylmercapturic acid in Chinese smokers.

    Science.gov (United States)

    Hou, Hongwei; Xiong, Wei; Gao, Na; Zhang, Xiaotao; Tang, Gangling; Hu, Qingyuan

    2012-11-01

    The acrylonitrile metabolites 2-cyanoethylmercapturic acid (CEMA) and 2-hydroxyethylmercapturic acid (HEMA) have been determined in human urine using an automated column-switching procedure. A diluted sample was centrifuged just prior to being injected into a reusable precolumn packed with a restricted access material and coupled to a liquid chromatography-tandem mass spectrometry system. This method achieved satisfactory reproducibility and accuracy. Average intra- and interday variations (% relative standard deviations) ranged from 2.4 to 3.8% for CEMA and from 2.7 to 10.5% for HEMA. The limits of quantification were 0.003 and 0.099ng/ml for CEMA and HEMA, respectively. It was used to study the uptake of acrylonitrile from smoke constituents by both nonsmokers and smokers of different tar yield cigarettes under ISO 3308 smoking condition. Metabolite concentrations in smoker urine samples were approximately 12 times higher compared with those in nonsmokers for CEMA and 3 times higher for HEMA. Urinary CEMA levels show a clear dose-response relationship with daily cigarette consumption and urinary cotinine. CEMA can also discriminate between smokers of different ISO cigarettes. Because HEMA is not specific, it is only slightly related to smoking and acrylonitrile exposure. The validated biomarker CEMA will continue to be useful for studies of acrylonitrile uptake by smokers.

  10. Synthesis of segmented (pb(ps-block-pb)(n)) and (pb(san-block- pb)(n)) block-copolymers via polymeric thermal iniferters

    NARCIS (Netherlands)

    Kroeze, E; ten Brinke, G.; Hadziioannou, G

    1995-01-01

    A technique is described for the synthesis of segmented poly(butadiene-block-styrene) block copolymers and segmented poly(butadiene-block-(styrene-co-acrylonitrile)) block copolymers through polybutadiene-based thermal iniferters. Dihydroxy- and dicarboxy-terminated polybutadienes were transformed i

  11. 16 CFR 1500.86 - Exemptions from classification as a banned toy or other banned article for use by children.

    Science.gov (United States)

    2010-01-01

    ... coil springs which expand when the article is subjected to a force that will extend the spring to its... (acrylonitrile butadiene styrene), nylon, and high-impact polystyrene) that are injection-molded and possess high..., or high-impact polystyrene) though exempt from the requirements that there be no internal voids,...

  12. Performance evaluation of a full-scale ABS resin manufacturing wastewater treatment plant: a case study in Tabriz Petrochemical Complex

    Directory of Open Access Journals (Sweden)

    Mohammad Shakerkhatibi

    2016-08-01

    Full Text Available Background: The measurement data regarding the influent and effluent of wastewater treatment plant (WWTP provides a general overview, demonstrating an overall performance of WWTP. Nevertheless, these data do not provide the suitable operational information for the optimization of individual units involved in a WWTP. A full-scale evolution of WWTP was carried out in this study via a reconciled data. Methods: A full-scale evolution of acrylonitrile, butadiene and styrene (ABS resin manufacturing WWTP was carried out. Data reconciliation technique was employed to fulfil the mass conservation law and also enhance the accuracy of the flow measurements. Daily average values from long-term measurements by the WWTP library along with the results of four sampling runs, were utilized for data reconciliation with further performance evaluation and characterization of WWTP. Results: The full-scale evaluation, based on balanced data showed that removal efficiency based on chemical oxygen demand (COD and biochemical oxygen demand (BOD5 through the WWTP were 80% and 90%, respectively, from which only 28% of COD and 20% of BOD5 removal had occurred in biological reactor. In addition, the removal efficiency of styrene and acrylonitrile, throughout the plant, was approximately 90%. Estimation results employing Toxchem model showed that 43% of acrylonitrile and 85% of styrene were emitted into the atmosphere above water surfaces. Conclusion: It can be concluded that the volatilization of styrene and acrylonitrile is the main mechanism for their removal along with corresponded COD elimination from the WWTP.

  13. High Technology Mass Spectrometry Laboratory

    Science.gov (United States)

    2010-08-01

    Corbett, F.W. Benz and R.S. Doyle. Acrylonitrile induces autolysis Bacillus subtilis. FEMS Microbiology Letters 182: 255-258 (2000). 25. Nerland, D.E., J...Supplement, 391 (1999). 24. Benz, F.W., J Li, D Corbett, T.S. Chen and D E Nerland. Neither Direct Chemical Nor Cyanide Antagonism Can Fully Explain The

  14. Preparation and characterization of poly(lithium acrylate-arcylonitrile)/LiClO4-LiNO3-LiBr solid polymer electrolytes

    Institute of Scientific and Technical Information of China (English)

    PAN Chun-yue; YUAN Yun-lan; CHEN Zhen-hua; XU Xian-hua; ZHANG Jian

    2005-01-01

    Through orthogonal experiment, a new type of LiClO4-LiNO3-LiBr eutectic salt with optimum mole ratio of n(LiClO4):n(LiNO3):n(LiBr)=1.6:3.8:1.0 was prepared. The poly(lithium acrylate-acrylonitrile)/LiClO4-LiNO3-LiBr solid polymer electrolytes were prepared with poly(lithium acrylate-acrylonitrile) and LiClO4-LiNO3-LiBr eutectic salts. The effect of LiClO4-LiNO3-LiBr eutectic salts content on the conductivity of solid polymer electrolytes was studied by alternating current impedance method, and the structures of eutectic salts and solid polymer electrolytes were characterized by differential thermal analysis, infrared spectroscopy and X-ray diffractometry. The results show that the room temperature conductivity of LiClO4-LiNO3-LiBr eutectic salts reaches 3.11×10-4 S·cm-1. The poly(lithium acrylate-acrylonitrile)/LiClO4-LiNO3-LiBr solid polymer electrolytes possess the highest room temperature conductivity at 70% LiClO4-LiNO3-LiBr eutectic salts content, and exhibit lower glass transition temperature of 75 ℃ compared with that of poly(lithium acrylate-acrylonitrile) of 105 ℃. A complex may be formed in the solid polymer electrolytes from the differential thermal analysis and infrared spectroscopy analysis. X-ray diffraction results show that the poly(lithium acrylate-acrylonitrile) can suppress the crystallization of eutectic salts in this system.

  15. Towards developing an efficient sensitive element for trinitrotoluene detection: TiO2 thin films functionalized with molecularly imprinted copolymer films

    Science.gov (United States)

    Lazau, Carmen; Iordache, Tanta-Verona; Florea, Ana-Mihaela; Orha, Corina; Bandas, Cornelia; Radu, Anita-Laura; Sarbu, Andrei; Rotariu, Traian

    2016-10-01

    In this study, TiO2 films were successfully grown in-situ onto a FTO substrate by a hydrothermal method, using TiCl4 as Ti precursor, and further on functionalized with a 2,4,6-trinitrotoluene-molecularly imprinted polymer (TNT-MIP) film as a preliminary step in developing a trinitrotoluene (TNT) reusable sensor to overcome the international security issues. For investigating the TiO2 film thickness, crystalline structure and morphology, the films were autoclaved at 200 °C at different times. The X-ray diffraction showed that TiO2 films possessed a rutile structure, with no cracks visible by atomic force microscopy (AFM), and the films morphology observed by scanning electron microscopy (SEM) was highly dependent upon the hydrothermal treatment time. Yet, the TiO2 films with a more porous surface were more suitable for TNT-MIP film deposit. Rheology of precursor polymer film solutions, based on poly (acrylonitrile-co-acrylic acid), poly (acrylonitrile-co-methacrylic acid) or poly (acrylonitrile- co-itaconic acid), and the structure and adherence of TNT-MIP films were investigated in order to establish the correct recipe of the MIP. The removal yield of TNT from the imprinted films, the thickness, the porosity and the compatibility with the inorganic TiO2 film were adequate for the poly (acrylonitrile-co-acrylic acid) system with an acrylonitrile: acrylic acid practical ratio of 86.1:13.9 (wt./wt.). Farmore, AFM morphology corroborated with SEM results highlighted the effect of TNT imprinting in the copolymer matrix as the surface of the imprinted layer was quite different from that of the non-imprinted layer.

  16. Enzymatic degradation of nitriles by a Candida guilliermondii UFMG-Y65.

    Science.gov (United States)

    Dias, J C; Rezende, R P; Rosa, C A; Lachance, M A; Linardi, V R

    2000-06-01

    Candida guilliermondii UFMG-Y65, isolated from a gold mine, was able to utilize different nitriles and the corresponding amides as sole source of nitrogen, at concentrations up to 2 M. Resting cells cultivated on YCB-acetonitrile medium showed nitrile hydrolyzing enzyme activities against acrylonitrile and benzonitrile. These enzymes were inducible and intracellular; the optimum pH was 7.0-8.0, and the optimum temperature 25 degrees C-30 degrees C. Liquid chromatographic analysis indicated that C. guilliermondii UFMG-Y65 metabolized 12 mM benzonitrile to 11 mM benzoic acid and 10 mM acrylonitrile to 7.9 mM acrylic acid. The results suggest that C. guilliermondii UFMG-Y65 may be useful for the bioproduction of amides and acids, and for the bioremediation of environments contaminated with nitriles.

  17. Synthesis of quaternary derivatives of ortho-coco di-amido toluene and investigation of these compounds as cationic bitumen emulsifier

    Energy Technology Data Exchange (ETDEWEB)

    Hassanzadeh, Masoumeh; Tayebi, Leila; Dezfouli, Hedieh; Kambarani, Masoud; Avval, Parviz Ahmadi [Tehran Univ. (Iran, Islamic Republic of). ACECR, Designing Chemical Process Research Group

    2012-05-15

    Bitumen emulsions are preferred over conventional pavement systems due to their biologically and environmentally acceptable formulation, safety, low viscosity, storage stability, and cost effectiveness. The present investigation deals with the systematic study to synthesize ortho-cocodi-amido toluene and four quaternary derivatives by amidation of coconut oil and ortho toluene diamine (OTD), followed by quaternization with formaldehyde, formic acid mixture, and acrylonitrile, resulted in a new quaternary compound useful as cationic emulsifier in bitumen emulsions. The roles of temperature and reaction time in determining optimum conditions were investigated as well. Emulsifying behavior of these quaternary compounds was studied by sieve residue test, settlement and storage stability test of emulsified asphalt, and water solubility. The results show that the acrylonitrile imidazolinium derivative of o-cocodi-amido toluene (VI) can be used as a rapid-medium setting emulsifier. (orig.)

  18. Rubber curing chemistry governing the orientation of layered silicate

    Directory of Open Access Journals (Sweden)

    2007-11-01

    Full Text Available The effect of curing systems on the orientation and the dispersion of the layered silicates in acrylonitrile butadiene rubber nanocomposite is reported. Significant differences in X-ray diffraction pattern between peroxide curing and sulfur curing was observed. Intense X-ray scattering values in the XRD experiments from peroxide cured vulcanizates indicate an orientation of the layers in a preferred direction as evinced by transmission electron micrographs. However, sulfur cured vulcanizates show no preferential orientation of the silicate particles. Nevertheless, a closer inspection of transmission electron microscopy (TEM images of peroxide and sulfur cured samples shows exfoliated silicate layers in the acrylonitrile butadiene rubber (NBR matrix. It was revealed in the prevailing study that the use of an excess amount of stearic acid in the formulation of the sulfur curing package leads to almost exfoliated type X-ray scattering pattern.

  19. Polybenzoxazole-filled nitrile butadiene rubber compositions

    Science.gov (United States)

    Gajiwala, Himansu M. (Inventor); Guillot, David G. (Inventor)

    2008-01-01

    An insulation composition that comprises at least one nitrile butadiene rubber (NBR) having an acrylonitrile content that ranges from approximately 26% by weight to approximately 35% by weight and polybenzoxazole (PBO) fibers. The NBR may be a copolymer of acrylonitrile and butadiene and may be present in the insulation composition in a range of from approximately 45% by weight to approximately 56% by weight of a total weight of the insulation composition. The PBO fibers may be present in a range of from approximately 3% by weight to approximately 10% by weight of a total weight of the insulation composition. A rocket motor including the insulation composition and a method of insulating a rocket motor are also disclosed.

  20. Preparation of n-tetradecane-containing microcapsules with different shell materials by phase separation method

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Rui [Department of Chemical Engineering, Tsinghua University, Beijing (China); Zhang, Yan; Zhang, Qingwu [Department of Chemical Engineering, China University of Mining and Technology, Beijing (China); Wang, Xin; Zhang, Yinping [Department of Building Science, Tsinghua University, Beijing (China)

    2009-10-15

    Microcapsules for thermal energy storage and heat-transfer enhancement have attracted great attention. Microencapsulation of n-tetradecane with different shell materials was carried out by phase separation method in this paper. Acrylonitrile-styrene copolymer (AS), acrylonitrile-styrene-butadiene copolymer (ABS) and polycarbonate (PC) were used as the shell materials. The structures, morphologies and the thermal capacities of the microcapsules were characterized using Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and differential scanning calorimetry (DSC). The ternary phase diagrams showed the potential encapsulation capabilities of the three shell materials. The effects of the shell/core ratio and the molecular weight of the shell material on the encapsulation efficiency and the thermal capacity of the microcapsules were also discussed. Microcapsules with melting enthalpy > 100 J/g, encapsulation efficiency 66-75%, particle size<1 {mu}m were obtained for all three shell materials. (author)

  1. Investigation of free volume and the interfacial, and toughening behavior for epoxy resin/rubber composites by positron annihilation

    Science.gov (United States)

    Minfeng, Zeng; Xudong, Sun; Huiquan, Xiao; Genzhong, Ji; Xuewen, Jiang; Baoyi, Wang; Chenze, Qi

    2008-03-01

    An epoxy resin (EP) matrix has been modified with carboxyl-randomized butadiene-acrylonitrile (CRBN) rubber and hydroxyl-terminated butadiene-acrylonitrile rubber (HTBN). When the rubber content was low (⩽5%), the free volume size varied slowly, meanwhile, the free volume size of EP/HTBN system was smaller than EP/CRBN system. With further addition of rubber component (⩾7%), the free volume size of the composite increased quickly. In this case, the free volume size of EP/HTBN system was larger than EP/CRBN system. The intermediate positron lifetime component ( I2) was affected by the structure of the interface layer between rubber particles and EP matrix. The different free volume properties could be attributed to the compatibility between rubber and EP.

  2. Investigation of free volume and the interfacial, and toughening behavior for epoxy resin/rubber composites by positron annihilation

    Energy Technology Data Exchange (ETDEWEB)

    Zeng Minfeng; Sun Xudong; Xiao Huiquan; Ji Genzhong; Jiang Xuewen [Institute of Applied Chemistry, Shaoxing University, Shaoxing 312000 (China); Wang Baoyi [Institute of High Energy Physics, Chinese Academy of Science, Beijing 100049 (China); Qi Chenze [Institute of Applied Chemistry, Shaoxing University, Shaoxing 312000 (China)], E-mail: Qichenze@zscas.edu.cn

    2008-03-15

    An epoxy resin (EP) matrix has been modified with carboxyl-randomized butadiene-acrylonitrile (CRBN) rubber and hydroxyl-terminated butadiene-acrylonitrile rubber (HTBN). When the rubber content was low ({<=}5%), the free volume size varied slowly, meanwhile, the free volume size of EP/HTBN system was smaller than EP/CRBN system. With further addition of rubber component ({>=}7%), the free volume size of the composite increased quickly. In this case, the free volume size of EP/HTBN system was larger than EP/CRBN system. The intermediate positron lifetime component (I{sub 2}) was affected by the structure of the interface layer between rubber particles and EP matrix. The different free volume properties could be attributed to the compatibility between rubber and EP.

  3. Blending protocol effect in structural properties of PA6/ABS nanocomposites compatibilized with SAN-MA; Influencia do protocolo de mistura nas propriedades estruturais de nanocompositos PA6/ABS compatibilizados com SAN-MA

    Energy Technology Data Exchange (ETDEWEB)

    Castro, Lucas D.C. de; Oliveira, Amanda D.; Pessan, Luiz Antonio, E-mail: lucasdanielcastro@hotmail.com, E-mail: pessan@ufscar.br [Universidade Federal de Sao Carlos (UFSCar), Sao Carlos, SP (Brazil). Programa de Pos-Graduacao em Ciencia e Engenharia de Materiais

    2013-07-01

    Nanocomposites based on polyamide 6 (PA6) and acrylonitrile-butadiene-styrene (ABS) compatibilized with styrene acrylonitrile-co-maleic anhydride were prepared using different blending protocols in a twin screw extruder. Specimen were prepared though injection molding. The organoclay (OMMT) incorporation and blending sequence effect on structural properties were investigated. X-ray diffraction analysis (XRD) indicates a complete exfoliated structure for all samples. Rheological measurements show an increasing in nanocomposites complex viscosities and storage modulus values when compared with the ternary blend. However, no significant effects in the rheological behavior were observed due the blending sequence. Differential scanning calorimetry (DSC) measurements suggests the incorporation of OMMT and different blending protocols may influence the polyamide polymorphism and degree of crystallinity. (author)

  4. Nitrile bioconversion by Microbacterium imperiale CBS 498-74 resting cells in batch and ultrafiltration membrane bioreactors.

    Science.gov (United States)

    Cantarella, M; Cantarella, L; Gallifuoco, A; Spera, A

    2006-03-01

    The biohydration of acrylonitrile, propionitrile and benzonitrile catalysed by the NHase activity contained in resting cells of Microbacterium imperiale CBS 498-74 was operated at 5, 10 and 20 degrees C in laboratory-scale batch and membrane bioreactors. The bioreactions were conducted in buffered medium (50 mM Na(2)HPO(4)/NaH(2)PO(4), pH 7.0) in the presence of distilled water or tap-water, to simulate a possible end-pipe biotreatment process. The integral bioreactor performances were studied with a cell loading (dry cell weight; DCW) varying from 0.1 mg(DCW) per reactor to 16 mg(DCW) per reactor, in order to realize near 100% bioconversion of acrylonitrile, propionitrile and benzonitrile without consistent loss of NHase activity.

  5. Rapid prototyping of polymeric microstructures with a UV laser

    DEFF Research Database (Denmark)

    Jensen, Martin F.; McCormack, John E.; Helbo, Bjarne

    2003-01-01

    ion implantation of the master tool to prolong the lifetime has also been investigated. For injection moulding, where the pressure and temperature is higher than in hot embossing a positive laser ablated Acrylonitrile-butadien-styrene co-polymer (ABS) structure was used, which subsequently has been...... electroplated to achieve a negative metal mould insert. The preliminary results have been encouraging. The total time from concept to realisation of a series of prototypes is 4-5 working days....

  6. Polar, Functional Diene-Based Materials: Free Radical Polymerization of 2-Cyanomethyl-1,3-Butadiene

    Energy Technology Data Exchange (ETDEWEB)

    Jing, Y [Iowa State Univ., Ames, IA (United States)

    2000-09-12

    This thesis presented here focuses on the synthesis of 2-cyanomethyl-l ,3-butadiene and the free-radical polymerization of this monomer. In addition to the bulk, solution and emulsion polymerizations,, copolymerization with styrene and acrylonitrile will also be discussed. The comonomers were chosen due to the potential applications mentioned above. Furthermore, the thermal properties and rnicrostructures of the homopolymers and the copolymers are examined.

  7. Toxicity of Pyrolysis Gases from Elastomers

    Science.gov (United States)

    Hilado, Carlos J.; Kosola, Kay L.; Solis, Alida N.; Kourtides, Demetrius A.; Parker, John A.

    1977-01-01

    The toxicity of the pyrolysis gases from six elastomers was investigated. The elastomers were polyisoprene (natural rubber), styrene-butadiene rubber (SBR), ethylene propylene diene terpolymer (EPDM), acrylonitrile rubber, chlorosulfonated polyethylene rubber, and polychloroprene. The rising temperature and fixed temperature programs produced exactly the same rank order of materials based on time to death. Acryltonitrile rubber exhibited the greatest toxicity under these test conditions; carbon monoxide was not found in sufficient concentrations to be the primary cause of death.

  8. Microwave Study of Recycled ABS Resins

    Institute of Scientific and Technical Information of China (English)

    A; M; Hasna

    2002-01-01

    This article provides a review of the research unde rt aken in order to determine the suitability of utilizing microwave technology in the production of Recycled ABS Acrylonitrile Butadiene Styrene resin for mouldin gs. The experimental investigation determined the suitability of the existing re cycled ABS material, the mould material used with respect to performance and lon gevity, potential commercial plant and equipment, end mould compression. Introduction Frequency Characterization of ABS The first ...

  9. Development of Carcinogenesis Bioassay Models: Response of Small Fish Species to Various Classes of Carcinogens

    Science.gov (United States)

    1991-12-20

    applications are pupfish (Poeciliopsis spp.), zebrafish (Brachydanio rerio), and platyfish/swordtail hybrids. 1 Number of animals and statistical design...I Introduction 1,2-Dibromoethane (DBE; ethylene dibromide) is a halogenated aliphatic hydrocarbon that has been used as a pesticide and gasoline...fumigant for stored tobacco, for flour milling and bakery food processing equipment, and in pesticides . As an industrial chemical, acrylonitrile is widely

  10. APPLICATION OF TIME-TEMPERATURE SUPERPOSITION PRINCIPLE TO EVALUATION OF SCATTERING INTENSITY EVOLUTION IN PHASE SEPARATION FOR PMMA/SAN BLENDS

    Institute of Scientific and Technical Information of China (English)

    Mao Peng; Qiang Zheng

    2000-01-01

    Spinodal phase separation behavior of poly(methyl methacrylate)/poly(styrene-co-acrylonitrile) (PMMA/SAN)blends was investigated by the time-resolved small angle light scattering (SALS) technique. It was found that the influence of temperature on the scattering intensity evolution followed the time-temperature superposition principle. The relationship between temperature and the relaxation time of scattering intensity I(t) can be well described by the Williams-Landel-Ferry (WLF) function.

  11. Ionic Liquids Applied to Improve the Dispersion of Coagent Particles in an Elastomer

    OpenAIRE

    Magdalena Maciejewska; Marian Zaborski

    2013-01-01

    The aim of this work was to study the activity of several ionic liquids (alkylimidazolium salts) that are used to improve the dispersion of coagent particles in peroxide-cross-linked hydrogenated acrylonitrile butadiene elastomer (HNBR). Hydrotalcite grafted with monoallyl maleate was applied as a coagent for the HNBR vulcanization. In this paper, we discuss the effect of the ionic liquids (alkylimidazolium salts) with respect to their anion (bromide, chloride, tetrafluoroborate, and hexafluo...

  12. PHOTOCOPOLYMERIZATION OF MALEIC ANHYDRIDE AND VINYL ACETATE

    Institute of Scientific and Technical Information of China (English)

    LI Xiaofang; LI Shanjun; QIN Anwei; YU Tongyin

    1990-01-01

    The charge-transfer complex of maleic anhydride and vinyl acetate was copolymerized under UV light. The chain composition and structure of the copolymer were analyzed with conductometry and NMR, and the chain sequence was determined as alternating. The copolymerization rates at different feed ratios, temperatures and in different solvents were investigated, giving evidence to the very active involvement of the CT complexes in the copolymerization. Terpolymerization with acrylonitrile also showed that the complex mechanism was a proper one for this system.

  13. Feasibility Study of Sensor Aided Impact Acoustic Sorting of Plastic Materials from End-of-Life Vehicles (ELVs)

    OpenAIRE

    Jiu Huang; Zhengfu Bian; Shaogang Lei

    2015-01-01

    The purpose of this feasibility research was to study a novel sensor based separation method for recycling of plastic materials from end-of-life vehicles (ELVs) by using eigen-frequency response of impact acoustic emission. In this research three kinds of commonly used plastics, polypropylene (PP), acrylonitrile-butadiene-styrene (ABS), and styrene-maleic-anhydride (SMA) sampled from end-of-life vehicles, were researched. Almost all the crushed plastic scraps had a flake structure, theoretica...

  14. Radiation Induced Crosslinking of Polyethylene in the Presence of Bifunctional Vinyl Monomers

    DEFF Research Database (Denmark)

    Joshi, M. S.; Singer, Klaus Albert Julius; Silverman, J.

    1977-01-01

    Several reports have been published showing that the radiation induced grafting of bifunctional vinyl monomers to low density polyethylene results in a product with an unusually high density of crosslinks. The same grafting reactions are shown to reduce the incipient gel dose by more than a factor...... of fifty. This paper is concerned with the apparent crosslinking produced by the radiation grafting of two monomers to polyethylene: acrylic acid and acrylonitrile....

  15. 40 CFR 60.667 - Chemicals affected by subpart NNN.

    Science.gov (United States)

    2010-07-01

    ... 107-89-1 Acetic acid 64-19-7 Acetic anhydride 108-24-7 Acetone 67-64-1 Acetone cyanohydrin 75-86-5 Acetylene 74-86-2 Acrylic acid 79-10-7 Acrylonitrile 107-13-1 Adipic acid 124-04-9 Adiponitrile 111-69-3... Butenes, mixed n-Butyl acetate 123-86-4 Butyl acrylate 141-32-2 n-Butyl alcohol 71-36-3 sec-Butyl...

  16. 40 CFR Table 1 to Subpart Eeee of... - Organic Hazardous Air Pollutants

    Science.gov (United States)

    2010-07-01

    ....2406. Compound name CAS No.1 2,4-D salts and esters 94-75-7 Acetaldehyde 75-07-0 Acetonitrile 75-05-8 Acetophenone 98-86-2 Acrolein 107-02-8 Acrylamide 79-06-1 Acrylic acid 79-10-7 Acrylonitrile 107-13-1 Allyl chloride 107-05-1 Aniline 62-53-3 Benzene 71-43-2 Biphenyl 92-52-4 Butadiene (1,3-) 106-99-0...

  17. Rheology of ABS and binary of organo clay nanocomposites; Reologia de nanocompositos de ABS e mistura binaria de argilas montmorilonita organofilicas

    Energy Technology Data Exchange (ETDEWEB)

    Galvan, Danieli; Mazzucco, Mateus; Carneiro, Fabio; Bartoli, Julio R.; Morales, Ana Rita, E-mail: bartoli@unicamp.br [Fac. de Engenharia Quimica/Universidade Estadual de Campinas-DTP/FEQ/UNICAMP-, SP (Brazil); D' Avila, Marcos A. [Fac. de Engenharia Mecanica/Universidade Estadual de Campinas - DEMA/FEM/UNICAMP, SP (Brazil)

    2011-07-01

    nanocomposites of poly(acrylonitrile-butadiene-styrene) and organically modified montmorillonite clays by melt intercalation on a co-rotating twin-screw extruder were prepared and characterized. It was studied the effects of screw torque and a binary mixture of organically modified montmorillonites on the intercalation/exfoliation of organoclays in the polymer matrix, characterized by X-ray diffraction morphological analyses and by capillary and parallel plates rheological analyses. (author)

  18. Rubber-Modified Epoxies. II. Morphology, Transitions, and Mechanical Properties.

    Science.gov (United States)

    1984-11-01

    tetrafunctional aromatic diamine-cured diglycidyl ether of bisphenol A ( DGEBA )-type epoxy resin was selected as the neat system because of its high ETgm (1670C...was a DGEBA -type epoxy resin (DER 331, Dow Chemical Co.) cured with tri- methylene glycol di-p-aminobenzoate (ITMABO, i.e. Polacure 740M, Polaroid...Chemical "o.) with excess of DGEBA resin. The second system, denoted DTAxl6, was iodified with a commercial amino-terminated butadiene-acrylonitrile

  19. Influence of the morphology on mechanical properties of toughened epoxies with CTBN

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Presents a toughened-epoxy risen based on diglycidylether of bisphenol A (DGEBA) cured with ethylene-diamine (EDA) and modified with a carboxyl-terminated acrylonitrile-butadiene (CTBN), studies morphologies with different rubber content and analyses the influence of rubber-phase morphology corresponding to different rubber contents on mechanical properties (elastic modulus, uniaxial compression yield stress, shearing strength, uneven tensile strength, critical stress intensity factor Kic and strain energy release rate Gic) of toughened epoxies.

  20. Biomonitoring of 1,3-butadiene and related compounds.

    OpenAIRE

    Osterman-Golkar, S; Bond, J. A.

    1996-01-01

    The 1990 Clean Air Act Amendments list several volatile organic chemicals as hazardous air pollutants, including ethylene oxide, butadiene, styrene, and acrylonitrile. The toxicology of many of these compounds shares several common elements such as carcinogenicity in laboratory animals, genotoxicity of the epoxide intermediates, involvement of cytochrome P450 for metabolic activation (except ethylene oxide), and involvement of at least two enzymes for detoxication of the epoxides (e.g., hydro...

  1. Polymer/Solvent and Polymer/Polymer Interaction Studies

    Science.gov (United States)

    1979-08-01

    experiment. The solvent trap prevents noxious, toxic, corrosive and carcinogenic solvents from escaping to the atmosphere. The sample is injected into the...a new apparatus was constructed to reflux the o-chlorophenol containing the PBT flakes without exposure to oxygen after the distillation. The reflux...Perfluorotributylamine J23 Dio-idomethane 01 Acetonitile J24 Pentachloroethane 02 Acrylonitrile J25 Tetrachloroethylene 03 Propionitrile J26 t,ct

  2. USSR Report, Chemistry

    Science.gov (United States)

    2007-11-02

    Sep 84) 89 Benzoyl Peroxide Initiated Polymerization of Acrylonitrile in Dimethylformamide (B. M. Sogomdnyan, G. S. Simonyan; ARMYANSKIY...sulfur, nitrogen, and metals, carbon monoxide, and carcinogenic substances— products of incomplete pyrolysis of organic fuels. 31 Of all the types of...factors to be considered. This is particularly troublesome since human exposure to a nitrogen atmosphere containing 6-10% oxygen has an insidious onset

  3. Validation of the U.S. Army’s Current Hazardous Waste Data

    Science.gov (United States)

    1990-04-01

    100 RATIO OF TOTAL SCORE TO POSSIBLE SCORE. I Z I 44 APPENDIX E: CARCINOGEN LIST Acetamide Acetophenetidin Acrylamide Acrylonitrile Actinomycin D... Carcinogen List 45 APPENDIX F: Priority Pollutants 48 APPENDIX G: Prioritization Example 52 DISTRIBUTION Acoession For NTIS GRA&I DTIC TAB Q Unannounced...Restoration Program (IRP) sites and the resulting exposure to humans and the environment rather than the materials themselves RCRA 3002 (b) requires that

  4. Synthetic Analogs of Phospholipid Metabolites as Antimalarials.

    Science.gov (United States)

    1979-07-01

    sintered glass funnel without exposure to air, and washed with water, 99% ethanol, and finally heptane. The catalyst in heptane was washed into the reaction...potent carcinogen , is likely to form. It is unlikely that the market for bis(hydroxymethyl)phosphinic acid is sufficient to justify a commercial... acrylonitrile either by itself or through its monoalkyl ester. Monoethyl hydrogen chloromethylphosphonite was pre- pared from chloromethylphosphonous

  5. Environmental Compliance Assessment and Management Program

    Science.gov (United States)

    1994-04-01

    2.12. Carcinogenic Hazardous Air Pollutant - any hazardous air pollutant recognized as known, prob- able, or potential human carcinogen by the U.S...Acetamide 60355 Acetonitrile 75058 Acetophenone 98862 2-Acetylaminofluorene 53963 Acrolein 107028 Acrylamide 79061 Acrylic acid 79107 Acrylonitrile ...health effects following short-term exposure from accidental releases and which are listed in Part 355 of 40 Code of Federal Regulations (CFR). 3.3

  6. Kinetics and Degradation Products of Trichloroethene.

    Science.gov (United States)

    1986-05-01

    hindrance. In early copolymerization studies the relative rates of addition of acrylonitrile , vinylacetate and styrene radical were determined. The...human carcinogen . 6. Anaerobic biodegradation of TCE operates via reductive dehalogenation. 7. More studies are needed to investigate these findings...Again, due to convection and direct exposure to air, volatilization would be expected to be a dominant fate mechanism. 72 D. VADOSE ZONE Much of the

  7. WATER RESISTANCE OF WOOD - PLASTIC COMPOSITES MADE FROM WASTE MATERIALS RESULTED IN THE FURNITURE MANUFACTURING PROCESS

    OpenAIRE

    Camelia COŞEREANU; Dumitru LICA; Ioan CURTU; Mariana-Domnica STANCIU

    2014-01-01

    The purpose of this paper is to present innovative wood-plastic composites made from waste materials such as ABS (acrylonitrile butadiene styrene) and wood shavings resulted in the furniture manufacturing process. From previous investigations (with regard to physical integrity and compactness of the panels), only mixtures ranging from a ratio of 100% ABS: 0% shavings to 80% ABS: 20% shavings were selected for water resistance testing. Swelling in thickness and water absorption for...

  8. Carbon fibers: precursor systems, processing, structure, and properties.

    Science.gov (United States)

    Frank, Erik; Steudle, Lisa M; Ingildeev, Denis; Spörl, Johanna M; Buchmeiser, Michael R

    2014-05-19

    This Review gives an overview of precursor systems, their processing, and the final precursor-dependent structure of carbon fibers (CFs) including new developments in precursor systems for low-cost CFs. The following CF precursor systems are discussed: poly(acrylonitrile)-based copolymers, pitch, cellulose, lignin, poly(ethylene), and new synthetic polymeric precursors for high-end CFs. In addition, structure-property relationships and the different models for describing both the structure and morphology of CFs will be presented.

  9. 共聚物-深剂体系的气液平衡:新UNIFAC基团热力学模型与实验研究%Vapor-Liquid Equilibrium of Copolymer+solvent Systems:Experimental Data and Thermodynamic Modeling with New UNIFAC groups

    Institute of Scientific and Technical Information of China (English)

    Rogério A.G. Sé; Martín Aznar

    2008-01-01

    Vapor-liquid equilibrium (VLE)data for copolymer solutions are necessary for several chemical processes.However,VLE data for copolymer solutions in the published report are rare.In this study.experimental VLE data for binary systems copolymer+solvent were obtained using a gravimetric-sorption apparatus.The studied systems were hexane+poly(21%acrylonitrile-co-butadiene),hexanc+poly(33%acrylonitrile-co-butadiene),hexane+poly(51%acrylonitrile-co-butadiene),hexanc+poly(23%styrene-co-butadiene),hexane+poly(45%styrene-co-butadiene),and benzene+poly(44%styrene-co-methyl methacrylate)in the range 50-70℃.The experimental data were correlated with the UNIFAC and Elbro-FV group contribution models for the activity coefficient.Two sets of functional groups had been used to represent the monomers in copolymers:literature groups and new proposed groups.The mean deviations between experimental and calculated mass fractions about 2.4%with ElbroFV and 13.3%witll Zhong were observed when the groups proposed in this study were USed.and of 3.5%for E1bro-FV and 13.2%for Zhong when literature groups were used.

  10. High-level expression in Corynebacterium glutamicum of nitrile hydratase from Rhodococcus rhodochrous for acrylamide production.

    Science.gov (United States)

    Kang, Mi-Suk; Han, Sang-Soo; Kim, Mi-Young; Kim, Bu-Youn; Huh, Jong-Pil; Kim, Hak-Sung; Lee, Jin-Ho

    2014-05-01

    The nhhBAG gene of Rhodococcus rhodochrous M33 that encodes nitrile hydratase (NHase), converting acrylonitrile into acrylamide, was cloned and expressed in Corynebacterium glutamicum under the control of an ilvC promoter. The specific enzyme activity in recombinant C. glutamicum cells was about 13.6 μmol/min/mg dry cell weight (DCW). To overexpress the NHase, five types of plasmid variants were constructed by introducing mutations into 80 nucleotides near the translational initiation region (TIR) of nhhB. Of them, pNBM4 with seven mutations showed the highest NHase activity, exhibiting higher expression levels of NhhB and NhhA than wild-type pNBW33, mainly owing to decreased secondary-structure stability and an introduction of a conserved Shine-Dalgarno sequence in the translational initiation region. In a fed-batch culture of recombinant Corynebacterium cells harboring pNBM4, the cell density reached 53.4 g DCW/L within 18 h, and the specific and total enzyme activities were estimated to be 37.3 μmol/min/mg DCW and 1,992 μmol/min/mL, respectively. The use of recombinant Corynebacterium cells for the production of acrylamide from acrylonitrile resulted in a conversion yield of 93 % and a final acrylamide concentration of 42.5 % within 6 h when the total amount of fed acrylonitrile was 456 g.

  11. Real-Time Small-Angle X-ray Scattering from Rubber-Modified Thermoplastics

    Science.gov (United States)

    Bubeck, R. A.

    1997-03-01

    Real-time small-angle X-ray scattering (RTSAXS) studies have been performed on a series of rubber-modified thermoplastics. These include: High Impact Polystyrene (HIPS), (2) Acrylonitrile Butadiene Styrene copolymers (ABS), (3) weatherable ABS-type resins containing grafted rubber particles derived from acrylonitrile ethylene styrene (AES) or acrylonitrile styrene acrylate (ASA), and (4) rubber-toughened syndiotactic polystyrene (sPS). Scattering patterns were measured at successive time intervals of from 2 to 3 ms. and were analyzed to determine the plastic strain due to crazing. Simultaneous measurements of the absorption of the primary beam by the sample allowed the total plastic strain to be computed. The plastic strain due to other deformation mechanisms (e.g. particle cavitation and macroscopic shear deformation) was determined by the difference. The contribution from microscopic shear deformation was determined from video-based optical data obtained along with the RTSAXS data. One example is an experimental AES system in an SAN matrix with insufficient gel particle graft which was found to lack substantial contributions from crazing and microshear yielding mechanisms. Manipulating the graft and cross linking levels in the AES system results in a ten-fold increase in microshear yield, but not much additional cavitation and crazing.

  12. Shock induced chemistry in liquids studied with ultrafast dynamic ellipsometry and visible transient absorption spectroscopy.

    Science.gov (United States)

    Dang, N C; Bolme, C A; Moore, D S; McGrane, S D

    2012-10-25

    The response to ultrafast laser shock loading of nine liquids was monitored in an effort to reveal evidence of chemical changes occurring during the first 350 ps following the shock front. In an effort to compare molecular structures possessing a variety of common bonding patterns, data were acquired for the liquids: cyclohexane, cyclohexene, 1,3-cyclohexadiene, benzene, water, acetonitrile, acrylonitrile, tert-butylacetylene, and phenylacetylene. Transient absorption spectra were measured in the spectral region from 440 to 780 nm over shock stress states from 7 to 20 GPa. Ultrafast dynamic ellipsometry was used to measure the shock and particle velocity as well as the shocked refractive index. Significant transient absorption attributed to chemical reaction was observed for shocked phenylacetylene and acrylonitrile. Evidence of volume decreasing chemical reactions was also observed in the ultrafast dynamic ellipsometry data for phenylacetylene and acrylonitrile. The liquid 1,3-cyclohexadiene exhibited volume decreasing reaction in the ultrafast dynamic ellipsometry data but did not exhibit an increase in the transient absorption spectra. There was no evidence of chemical reaction in cyclohexane, cyclohexene, benzene, water, acetonitrile, or tert-butylacetylene in the first 350 ps, despite the application of shock stress that was in many cases well above the reaction threshold observed at microsecond time scales.

  13. Towards developing an efficient sensitive element for trinitrotoluene detection: TiO{sub 2} thin films functionalized with molecularly imprinted copolymer films

    Energy Technology Data Exchange (ETDEWEB)

    Lazau, Carmen [National Institute for Research and Development in Electrochemistry and Condensed Matter, Condensed Matter Department, 1 P. Andronescu Street, 300224 Timisoara (Romania); Iordache, Tanta-Verona [National Research and Development Institute for Chemistry and Petrochemistry INCDCP-ICECHIM, Advanced Polymer Materials and Polymer Recycling, 202 Splaiul Independentei, 060021 Bucharest (Romania); Florea, Ana-Mihaela [National Research and Development Institute for Chemistry and Petrochemistry INCDCP-ICECHIM, Advanced Polymer Materials and Polymer Recycling, 202 Splaiul Independentei, 060021 Bucharest (Romania); University Politehnica of Bucharest, The Faculty of Applied Chemistry and Materials Science, Bioresources and Polymer Science Department, 1-7 Polizu, 011061 Bucharest (Romania); Orha, Corina [National Institute for Research and Development in Electrochemistry and Condensed Matter, Condensed Matter Department, 1 P. Andronescu Street, 300224 Timisoara (Romania); Bandas, Cornelia, E-mail: cornelia.bandas@gmail.com [National Institute for Research and Development in Electrochemistry and Condensed Matter, Condensed Matter Department, 1 P. Andronescu Street, 300224 Timisoara (Romania); Radu, Anita-Laura; Sarbu, Andrei [National Research and Development Institute for Chemistry and Petrochemistry INCDCP-ICECHIM, Advanced Polymer Materials and Polymer Recycling, 202 Splaiul Independentei, 060021 Bucharest (Romania); Rotariu, Traian [Technical Military Academy, Chemistry Department, Bucharest (Romania)

    2016-10-30

    Highlights: • A new concept for creating reusable and more sensitive sensors for trinitrotoluene. • Titanium oxide thin films as transducers deposited by a new hydrothermal process. • Trinitrotoluene-molecularly imprinted receptors obtained by a two-step procedure. - Abstract: In this study, TiO{sub 2} films were successfully grown in-situ onto a FTO substrate by a hydrothermal method, using TiCl{sub 4} as Ti precursor, and further on functionalized with a 2,4,6-trinitrotoluene-molecularly imprinted polymer (TNT-MIP) film as a preliminary step in developing a trinitrotoluene (TNT) reusable sensor to overcome the international security issues. For investigating the TiO{sub 2} film thickness, crystalline structure and morphology, the films were autoclaved at 200 °C at different times. The X-ray diffraction showed that TiO{sub 2} films possessed a rutile structure, with no cracks visible by atomic force microscopy (AFM), and the films morphology observed by scanning electron microscopy (SEM) was highly dependent upon the hydrothermal treatment time. Yet, the TiO{sub 2} films with a more porous surface were more suitable for TNT-MIP film deposit. Rheology of precursor polymer film solutions, based on poly (acrylonitrile-co-acrylic acid), poly (acrylonitrile-co-methacrylic acid) or poly (acrylonitrile- co-itaconic acid), and the structure and adherence of TNT-MIP films were investigated in order to establish the correct recipe of the MIP. The removal yield of TNT from the imprinted films, the thickness, the porosity and the compatibility with the inorganic TiO{sub 2} film were adequate for the poly (acrylonitrile-co-acrylic acid) system with an acrylonitrile: acrylic acid practical ratio of 86.1:13.9 (wt./wt.). Farmore, AFM morphology corroborated with SEM results highlighted the effect of TNT imprinting in the copolymer matrix as the surface of the imprinted layer was quite different from that of the non-imprinted layer.

  14. Graft copolymerization of acrylo–nitrile onto delignified native bamboo (Bambusa vulgaris cellulosic and its utilization potential for heavy metal uptake from aqueous medium

    Directory of Open Access Journals (Sweden)

    M.O. EKEBAFE

    2011-06-01

    Full Text Available Graft polymerization of acrylonitrile onto delingnified cellulosic material obtained from Nigeria grown bamboo (Bambusa vulgaris could be initiated by a ceric ammonium nitrate redox system. Optimization of grafting of acrylonitrile onto cellulosic material was performed by varying the reaction conditions, such as the duration of soaking of cellulosic material in ceric ammonium nitrate solution, concentration of ceric ammonium nitrate solution, polymerization time, temperature of reaction, and acrylonitrile concentration and saponification time, in order to study their influence on percent grafting yield and grafting efficiency. The resulting cellulosic-g-polyacrylonitrile (PAN copolymers were fractionated by extraction at 33 C with N,N’-dimethylformamide. Fractions were characterized by determining both the % add-on and the free polymer. Saponification of grafted copolymer was done by reaction with sodium hydroxide followed by methanol precipitation. The absorbent polymer so produced gave fair water retention values. The optimum reaction conditions obtained were: 20 mmol/L ceric ammonium nitrate solution in 1% nitric acid, soaking duration of 0.5 h at 40 C for a polymerization time of 2 h and saponification time of 3 h. The percent grafting was 167.89%, grafting efficiency was 93.52% and water retention value was 389 g/g. The grafting was confirmed using FTIR. Sorption of different metal ions in the mixture, e.g. Cr, Mn, Ni, Cu and Pb, by grafted cellulosic and the hydrogel was also investigated. Hydrolysis increases the sorption affinity of grafted cellulose toward water and metal ions.

  15. [The novel copolymer coated capillary columns of electrophoresis and their applications to separation of proteins].

    Science.gov (United States)

    Lu, G; Gao, D; Gu, J; Fu, R; Li, F; Zhang, H

    1999-01-01

    The copolymer of acrylonitrile, methyl acrylate, hydroxy ethyl acrylate (ZB-004), the copolymer of acrylonitrile, methyl acrylate, hydroxy ethyl acrylate, acrylamide (ZB-014) and the copolymer of acrylonitrile, hydroxy ethyl acrylate (ZB-016) were coated on the inner surface of fused-silica capillaries by just filling the capillary with solutions containing these copolymers followed by flushing the capillary with nitrogen. The physically adsorbed layer can reduce both protein adsorption and electroosmotic flow in the pH range of 3-5. Electroosmotic flow decreased by raising the concentrations of the copolymers. Separation performance of ZB-004 layer is better than those of other two layers due to its low hydrophilicity, but with higher pH values, appreciable peak deformation and increase in electroosmosis were observed. The intra day and inter day migration reproducibility were investigated in terms of relative standard deviation (RSD) with four basic proteins at pH 4.0. The RSDs of the intra day migration times were less than 2%. The RSDs of the inter day migration times were less than 4%. At pH 5.0, the RSDs of the migration times in two ZB-004-coated capillaries made on two different days were less than 1%. Separation efficiencies of four basic proteins in a ZB-004-coated capillary which stored in a buffer (pH 4.0) for fifteen days after being used for 14 days decreased 15%. These coatings were stable and exhibited reproducible separations from intra day, inter day and inter column under acidic conditions.

  16. Influence of Layer Thickness and Raster Angle on the Mechanical Properties of 3D-Printed PEEK and a Comparative Mechanical Study between PEEK and ABS

    Directory of Open Access Journals (Sweden)

    Wenzheng Wu

    2015-09-01

    Full Text Available Fused deposition modeling (FDM is a rapidly growing 3D printing technology. However, printing materials are restricted to acrylonitrile butadiene styrene (ABS or poly (lactic acid (PLA in most Fused deposition modeling (FDM equipment. Here, we report on a new high-performance printing material, polyether-ether-ketone (PEEK, which could surmount these shortcomings. This paper is devoted to studying the influence of layer thickness and raster angle on the mechanical properties of 3D-printed PEEK. Samples with three different layer thicknesses (200, 300 and 400 μm and raster angles (0°, 30° and 45° were built using a polyether-ether-ketone (PEEK 3D printing system and their tensile, compressive and bending strengths were tested. The optimal mechanical properties of polyether-ether-ketone (PEEK samples were found at a layer thickness of 300 μm and a raster angle of 0°. To evaluate the printing performance of polyether-ether-ketone (PEEK samples, a comparison was made between the mechanical properties of 3D-printed polyether-ether-ketone (PEEK and acrylonitrile butadiene styrene (ABS parts. The results suggest that the average tensile strengths of polyether-ether-ketone (PEEK parts were 108% higher than those for acrylonitrile butadiene styrene (ABS, and compressive strengths were 114% and bending strengths were 115%. However, the modulus of elasticity for both materials was similar. These results indicate that the mechanical properties of 3D-printed polyether-ether-ketone (PEEK are superior to 3D-printed ABS.

  17. Research progress of UV degradation of PVC/styrene-containing polymer blends%PVC/苯乙烯类聚合物共混体系紫外光降解研究进展

    Institute of Scientific and Technical Information of China (English)

    江天凯; 张军

    2013-01-01

      综述了丙烯腈-丁二烯-苯乙烯共聚物(ABS)、甲基丙烯酸甲酯-丁二烯-苯乙烯共聚物(MBS)、丙烯腈-氯化聚乙烯-苯乙烯共聚物(ACS)和丙烯腈-苯乙烯-丙烯酸酯共聚物(ASA)等苯乙烯类聚合物与聚氯乙烯共混得到的四种共混体系紫外光降解研究进展。其中,由于ABS和MBS主链结构中含有不饱和双键,在紫外光作用下易氧化降解,所以与聚氯乙烯共混体系耐候性较差;而ACS和ASA主链结构不含有不饱和双键,与聚氯乙烯的共混体系耐候性较好。%  This paper reviewed the research progress of UV degradation of poly(vinyl chloride)(PVC)/styrene-containing polymers blends. The four styrene-containing polymers were acrylonitrile-butadiene-styrene copolymer(ABS), methyl methacrylate-butadiene-styrene copolymer(MBS),acrylonitrile-chlorinated polyethy-lene-styrene copolymer(ACS) and acrylonitrile-styrene-acrylate copolymer(ASA). The reason that the PVC/ABS and PVC/MBS blends showed poor aging resistance was that there were unsaturated double bonds in the main chain of ABS and MBS and the unsaturated double bonds occurred oxidative degradation easily by UV irra-diation. On the contrary, the PVC/ACS and PVC/ASA blends showed relatively good aging resistance since there were no unsaturated double bonds in the main chain of ACS and ASA.

  18. Experimental study on nanofiltration treatment of high-concentration acryionitrile industrial wastewater%纳滤处理高浓度丙烯腈工业废水的实验研究

    Institute of Scientific and Technical Information of China (English)

    李薇; 展侠; 李继定; 郑冬菊

    2011-01-01

    The existing treatment technologies for high concentration acrylonitrile industrial wastewater are unsatisfactory. Aiming at the high concentration acrylonitrile industrial wastewater, the flocculation effects of five different flocculants were experimented by flocculation and nanofiltration processing. The optimal flocculant and amount were chosen, and the effect of nanofiltration was investigated. About 20% CODCr in the wastewater was removed through the flocculation process, and about 70% CODCr was removed through nanofiltration process. After nanofiltration in twice, the colourity and turbidity of wastewater come up to standard, which is very important for the circulating utilization of acrylonitrile industrial wastewater.%高浓度丙烯腈工业废水的处理技术在工业生产中都不理想,针对高浓度丙烯腈工业废水,采用絮凝和纳滤进行处理,测试了5种不同的絮凝剂的絮凝效果,选择最佳的絮凝剂及其用量,考察了纳滤处理高浓度丙烯腈废水的效果.经过絮凝过程除去废水中约20%的CODcr,纳滤过程除去约70%的CODcr,经过二次纳滤,废水出水色度、浊度已经达到出水指标,为实现丙烯腈生产中工业废水的绿色循环利用和零排放奠定了基础.

  19. No-carrier-added [1.sup.11 c]putrescine

    Science.gov (United States)

    McPherson, Daniel W.; Fowler, Joanna S.; Wolf, Alfred P.

    1989-01-01

    The invention relates to a new radiolabeled imaging agent, no-carrier-added [1-.sup.11 C]putrescine, and to the use of this very pure material as a radiotracer with positron emission tomography for imaging brain tumors. The invention further relates to the synthesis of no-carrier-added [1-.sup.11 C]putrescine based on the Michael addition of potassium .sup.11 C-labeled cyanide to acrylonitrile followed by reduction of the .sup.11 C-labeled dinitrile. The new method is rapid and efficient and provides radiotracer with a specific activity greater than 1.4 curies per millimol and in a purity greater than 95%.

  20. A low-cost lead-acid battery with high specific-energy

    Indian Academy of Sciences (India)

    S K Martha; B Hariprakash; S A Gaffoor; D C Trivedi; A K Shukla

    2006-01-01

    Lightweight grids for lead-acid battery grids have been prepared from acrylonitrile butadiene styrene (ABS) copolymer followed by coating with lead. Subsequently, the grids have been electrochemically coated with a conductive and corrosion-resistant layer of polyaniline. These grids are about 75% lighter than those employed in conventional lead-acid batteries. Commercial-grade 6V/3.5Ah (C20-rate) lead-acid batteries have been assembled and characterized employing positive and negative plates constituting these grids. The specific energy of such a lead-acid battery is about 50 Wh/kg. The batteries can withstand fast charge-discharge duty cycles.

  1. Investigation of thermal oxidative break-down of polyethylene films modified with grafted polyacrylonitrile. [Gamma radiation

    Energy Technology Data Exchange (ETDEWEB)

    Krul, L.P.; Gert, E.V. (Belorusskij Gosudarstvennyj Univ., Minsk)

    1981-11-01

    Thermal oxidative destruction of polyethylene (PE) films modified by radiation (..gamma..-radiation, dose rate is 0.56 Mrad/hr) liquid-phase graft polymerization of acrylonitrile (AN) has been studied. Comparative stability of grafted copolymers, homopolymers and mechanical mixtures of PE and PAN (polyacrylonitrile) to thermal oxidative destruction is studied using the derivatographic method. It is shown that graft of PAN considerably decelerates the development of oxidative and destructive processes in PE, at that, the efficiency of PE chain stabilization increases with the increase of grafted PAN amount. The sample with PAN content x=0.367 (in parts of the mass of grafted film) possesses the highest stability.

  2. SUSPENSION-SWELLING GRAFT COPOLYMERIZATION——SYNTHESIS OF ACS RESINS

    Institute of Scientific and Technical Information of China (English)

    WENG Zhixue; LOU Jianfeng; HUANG Zhiming; PAN Zuren

    1993-01-01

    Acrylonitrile (AN)-chlorinated polyethylene (CPE)-styrene (St) (ACS) terpolymer was synthesized by suspen sion-swelling graft copolymerization method, in which two key factors such as dispersing system and swelling time were studied. Highly effective complex dispersing system was chosen and determine, and two-layer protection modelwas put forward to clarify the stable effect mechanism. Varying the swelling time of CPE in AN and St monomer mixture, some results such as grafting effect, particle characteristics, rubber particle morphology and its size distribution, and properties of ACS resins were investigated , thus the optimum swelling time was proposed.

  3. Production of super-smooth articles

    Energy Technology Data Exchange (ETDEWEB)

    Duchane, D.V.

    1981-05-29

    Super-smooth rounded or formed articles made of thermoplastic materials including various poly(methyl methacrylate) or acrylonitrile-butadiene-styrene copolymers are produced by immersing the articles into a bath, the composition of which is slowly changed with time. The starting composition of the bath is made up of at least one solvent for the polymer and a diluent made up of at least one nonsolvent for the polymer and optional materials which are soluble in the bath. The resulting extremely smooth articles are useful as mandrels for laser fusion and should be useful for a wide variety of other purposes, for example lenses.

  4. OPTIMIZATION AND APPLICATIONS OF REVERSE-FLOW CYCLONES

    Institute of Scientific and Technical Information of China (English)

    Guogang Sun; Jianyi Chen; Mingxian Shi

    2005-01-01

    An optimum design approach to reverse-flow cyclones based on the concept of optimizing cyclone dimensions is introduced in this paper. This approach involves optimizing cyclone dimensions by categories, calculating cyclone performance by correlating similitude numbers and optimizing the combination of four cyclone parameters, D, KA,(-d- and vi, which has been proven to be applicable not only for single-stage cyclone, but also for multistage cyclone separators. Applications of the designed cyclones in FCC units and acrylonitrile reactors are also presented.

  5. Oxidation of phenyl alanine by pyridinium chlorochromate in acidic DMF–water medium: A kinetic study

    Directory of Open Access Journals (Sweden)

    B.L. Hiran

    2016-11-01

    Full Text Available The kinetics of oxidation of phenyl alanine by pyridinium chlorochromate in DMF–water (70:30% mixture in presence of perchloric acid leads to the formation of corresponding aldehyde. The reaction is of first order each in [PCC], [HClO4] and [AA]. Michaelis–Menten type kinetics was observed with phenyl alanine. The reaction rates were determined at different temperatures [25, 30, 35, 40, 45, 50 °C] and the activation parameters were calculated. The reaction does not induce polymerization of acrylonitrile. With an increase in the amount of DMF in its aqueous mixture, the rate increases. A suitable mechanism for the reaction was postulated.

  6. Crosslinked blends and coextruded films by electron beam

    Science.gov (United States)

    Vallat, M. F.; Marouani, S.; Perraud, S.; Mendoza Patlan, N.

    2005-07-01

    Morphology, thermal and mechanical properties of polymer blends and coextruded films of hydrogenated copolymer of butadiene and acrylonitrile (HNBR) and polyethylene-co-octene (PE-co-O) are considered before and after electron beam crosslinking. It is known that the properties are depending not only on the crosslinks in the bulk of the polymers but also on that created in the interfacial domain. It is however very difficult to have direct evidence of the interfacial crosslinks. Moreover the two polymers are not compatible and the addition of an ethylene vinyl acetate copolymer as a potential polymer compatibiliser is considered.

  7. Environmental Exposure and Accelerated Testing of Rubber-to-Metal Vulcanized Bonded Assemblies

    Science.gov (United States)

    1974-11-01

    subjected to the hydrolytic stability test or when exposed to the severe climatic conditions at Panama. EPDM and nitrile vulcanized bonded-specimens...butadiene acrylonitrile rubber bonded Sassembliesshowed a severe loes of 100 percent in bond strength; the EPDM bond.ed assemblies shcwed a 40 percent lose...02 ~ 4 -0 04 0: 00 V 4 o ~no 󈧄 0 80 EPDM Spgcimens aged up to 450°F are .shown .in Table 7. At 3000F, all - bonding agents provided good retention

  8. Thin flexible intercalation anodes

    Energy Technology Data Exchange (ETDEWEB)

    Levy, S.C.; Cieslak, W.R.; Klassen, S.E.; Lagasse, R.R.

    1994-10-01

    Poly(acrylonitrile) fibers have been pyrolyzed under various conditions to form flexible carbon yarns capable of intercalating lithium ions. These fibers have also been formed into both woven and non woven cloths. Potentiostatic, potentiodynamic and galvanostatic tests have been conducted with these materials in several electrolytes. In some tests, a potential hold was used after each constant current charge and discharge. These tests have shown some of these flexible materials to reversibly intercalate lithium ions to levels that are suitable for use as a practical battery anode.

  9. Charpy Impact Test on Polymeric Molded Parts

    Directory of Open Access Journals (Sweden)

    Alexandra Raicu

    2012-09-01

    Full Text Available The paper presents the Charpy impact tests on the AcrylonitrileButadiene-Styrene (ABS polymeric material parts. The Charpy impact test, also known as the Charpy V-notch test, is a standardized strain rate test which determines the amount of energy absorbed by a material during fracture. This is a typical method described in ASTM Standard D 6110. We use for testing an Instron - Dynatup equipment which have a fully integrated hardware and software package that let us capture load information at very high speed from the impact tests.

  10. Development of recycled plastic composites for structural applications from CEA plastics

    Science.gov (United States)

    Bhalla, Agrim

    Plastic waste from consumer electronic appliances (CEAs) such as computer and printer parts including Polystyrene (PS), Acrylonitrile Butadiene Styrene (ABS), Polystyrene (PS) and PC/ABS were collected using handheld FTIR Spectrophotometer. The blends of these plastics with High Density Polyethylene (HDPE) are manufactured under special processing conditions in a single screw compounding injection molding machine. The blends are thermoplastics have high stiffness and strength, which may enhance the mechanical properties of HDPE like tensile modulus, ultimate tensile strength, tensile break and tensile yield. These composites have a potential to be used for the future application of recycled plastic lumber, thus replacing the traditional wood lumber.

  11. Aza-Michael Mono-addition Using Acidic Alumina under Solventless Conditions

    Directory of Open Access Journals (Sweden)

    Giovanna Bosica

    2016-06-01

    Full Text Available Aza-Michael reactions between primary aliphatic and aromatic amines and various Michael acceptors have been performed under environmentally-friendly solventless conditions using acidic alumina as a heterogeneous catalyst to selectively obtain the corresponding mono-adducts in high yields. Ethyl acrylate was the main acceptor used, although others such as acrylonitrile, methyl acrylate and acrylamide were also utilized successfully. Bi-functional amines also gave the mono-adducts in good to excellent yields. Such compounds can serve as intermediates for the synthesis of anti-cancer and antibiotic drugs.

  12. Synthesis and characterization of castor oil based polyurethane–polyacrylonitrile interpenetrating polymer networks

    Indian Academy of Sciences (India)

    P Mallu; Siddaramaiah; R Somashekar

    2000-10-01

    A series of interpenetrating polymer networks (IPNs) of castor oil based polyurethane/polyacrylonitrile (PU/PAN: 80/20, 60/40, 50/50, 40/60 and 20/80) were synthesized by condensation reaction of castor oil with methylene diisocyanate and acrylonitrile, employing benzoyl peroxide (BPO) and ethylene glycol dimethylacrylate (EGDM) as initiator and crosslinkers respectively. The physical, chemical, optical and some of the mechanical properties of PU/PAN were studied. Phase stabilization in IPNs was investigated by wide angle X-ray (WAXS) profile analysis. Variation of crystal size distribution was studied in these polymer networks.

  13. 40 CFR Table 1 to Subpart Dd of... - List of Hazardous Air Pollutants (HAP) for Subpart DD

    Science.gov (United States)

    2010-07-01

    ...-05-8 Acetonitrile 0.989 98-86-2 Acetophenone 0.314 107-02-8 Acrolein 1.000 107-13-1 Acrylonitrile 0.999 107-05-1 Allyl chloride 1.000 71-43-2 Benzene (includes benzene in gasoline) 1.000 98-07-7...(chloromethyl)ether b 0.999 75-25-2 Bromoform 0.998 106-99-0 1,3-Butadiene 1.000 75-15-0 Carbon disulfide...

  14. Advanced resin systems for graphite epoxy composites

    Science.gov (United States)

    Gilwee, W. J.; Jayarajan, A.

    1980-01-01

    The value of resin/carbon fiber composites as lightweight structures for aircraft and other vehicle applications is dependent on many properties: environmental stability, strength, toughness, resistance to burning, smoke produced when burning, raw material costs, and complexity of processing. A number of woven carbon fiber and epoxy resin composites were made. The epoxy resin was commercially available tetraglycidylmethylene dianiline. In addition, composites were made using epoxy resin modified with amine and carboxyl terminated butadiene acrylonitrile copolymer. Strength and toughness in flexure as well as oxygen index flammability and NBS smoke chamber tests of the composites are reported.

  15. Temperature Effect on Mechanical Properties of NBR-based Stator Rubber for Progressing Cavity Pump%螺杆泵定子用丁腈基橡胶的温度力学效应

    Institute of Scientific and Technical Information of China (English)

    赵海超; 王世杰; 王慧明; 吕晓仁

    2015-01-01

    In order to improve the service life of stator rubber used in the progressing cavity pump stator, NBR based rubbers with different acrylonitrile contents are chosen as the experimental materials and their variations in weight, volume, tensile strength and so on before and after immersion experiment are investigated according to the actual work environment. The results show that with an increase in the tempera-ture of crude oil, the weight, volume and elongation at break of the NBR rubber with low acrylonitrile content increase and its hardness de-creases, while the NBR rubber with high acrylonitrile content shows the opposite tendency. The tensile strength of three kinds of NBR rub-bers decreases with the increase in the temperature of crude oil. The NBR rubber with high acrylonitrile content shows the better heat resis-tance and mechanical performance due to its dense microstructure.%为提高螺杆泵定子橡胶的使用寿命,从螺杆泵的实际工作环境出发,以不同丙烯腈含量的丁腈橡胶为试验材料,通过测试试样在原油介质中质量、体积以及抗拉强度的一系列变化,研究定子橡胶的温度力学效应。结果表明:随着原油温度的升高,低丙烯腈丁腈橡胶的质量、体积和扯断伸长率逐渐增大,硬度逐渐降低;而高丙烯腈丁腈橡胶则显示相反的规律。三种橡胶的抗拉强度随着原油温度的升高逐渐降低。高丙烯腈含量的丁腈橡胶由于致密的组织结构具有良好的耐热性和力学性能。

  16. Mechanical Spectroscopy of Nanostructured Composite Materials

    Energy Technology Data Exchange (ETDEWEB)

    Mari, Daniele; Schaller, Robert; Mazaheri, Mehdi, E-mail: daniele.mari@epfl.ch [Ecole Polytechnique Federale de Lausanne, Laboratoire de Physique de la Matiere Complexe, Groupe de Spectroscopie Mecanique, CH-1015 Lausanne (Switzerland)

    2011-07-06

    The thermo-mechanical behavior of different nano-structured composite materials, which were processed within the SAPHIR European Integrated Project, has been characterized by mechanical spectroscopy. The obtained results show clearly that creep resistance of fine grain ceramics such as zirconia can be improved by carbon nano-tube (CNT) reinforcements. On the other hand the elastic modulus and the damping capacity of aluminum matrix composites were increased by SiC nano-particle additions. It has also been observed that CNT additions are responsible for a better thermal stability of polymer such as ABS (Acrylonitrile-Butadiene-Styrene) used in automotive industry.

  17. STUDY ON STABILITY OF STRUCTURE AND PROPERTIES OF TIOPC/SAN PHOTOCONDUCTIVE COMPOSITES

    Institute of Scientific and Technical Information of China (English)

    Qiang Zheng; Li-fang Tong; Li-wei Li; Mang Wang

    2003-01-01

    The influence of the condensed structure of poly(styrene-co-acrylonitrile) (SAN) and traces of tetrahydrofuran (THF) that remained in titanyl phthalocyanine (TiOPc)/SAN films after fabrication on the photoconductive stability of TiOPc/SAN composites is studied. The results reveal that the existence of traces of THF results in the increase of the photoconductivity and the charging voltage. The main factors responsible for the unstable photoconductivity of the photoconductors are believed to be the relaxation of SAN and the slow volatilization of THF.

  18. Cross metathesis of unsaturated epoxides for the synthesis of polyfunctional building blocks

    Directory of Open Access Journals (Sweden)

    Meriem K. Abderrezak

    2015-10-01

    Full Text Available The cross metathesis of 1,2-epoxy-5-hexene (1 with methyl acrylate and acrylonitrile was investigated as an entry to the synthesis of polyfunctional compounds. The resulting cross metathesis products were hydrogenated in a tandem fashion employing the residual ruthenium from the metathesis step as the hydrogenation catalyst. Interestingly, the epoxide ring remained unreactive toward this hydrogenation method. The saturated compound resulting from the cross metathesis of 1 with methyl acrylate was transformed by means of nucleophilic ring-opening of the epoxide to furnish a diol, an alkoxy alcohol and an amino alcohol in high yields.

  19. A -cyanostilbene-modified Schiff base as efficient turn-on fluorescent chemosensor for Zn2+

    Indian Academy of Sciences (India)

    Aixiang Ding; Fang Tang; Tao Wang; Xutang Tao; Jiaxiang Yang

    2015-03-01

    A novel Schiff base derivative (Z)-3-(4-(hexyloxy)phenyl)-2-(4-((E)-2-hydroxybenzylidene amino)phenyl)acrylonitrile (L) was designed, synthesized and characterized. L was used as a Zn2+ selective, turn-on, fluorescent chemosensor with a detection limit of 0.1M in DMF. 1:1 stoichiometric complex formation of L wih Zn2+ was confirmed through fluorescent titration experiments and Job’s plot. The enhancement of fluorescence intensity of L with addition of Zn2+ is the consequence of the inhibited isomerization of the C=N bond, namely chelation-enhanced fluorescence (CHEF) effect.

  20. Short Fibre and Particulate-reinforced Rubber Composites

    Directory of Open Access Journals (Sweden)

    Kavita Agarwal

    2002-07-01

    Full Text Available Particulate fillers (carbon black and silica and short fibre (aromatic polyamide, Kevlar have been utilised to produce rubber composites based on acrylonitrile-co-butadiene rubber (NBR. Mechanical properties of these composites have been determined and compared with unfilled rubber vulcanisate. The effect of surface treatment on the improvement of strength, in case of Kevlar, has also been considered. The influence of elevated temperature on tear strength, an important failure criterion, has been evaluated. Scanning electron microscopy has been used as a tool to correlate the topographical features associated with changes in the tear strength of the composites.

  1. Cooling simulation of plastic injection molding

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Analyses the cooling of mold and plastic part during injectionmolding and the continued cooling of plastic part after being ejected from mold using the heat transfer theory and Boundary Element Method (BEM) to predict the temperature distribution in both mold and plastic part,and presents the experiments carried out with plates of ABS (Acrylonitrile-Butadiene-Styrene) to verify the validity of the cooling analysis software used to simulate the temperature distribution in ABS plate parts, and concludes that the analysis software agree qualitatively well with actual experimental findings.

  2. The cross linking of EPDM and NBR rubber

    Directory of Open Access Journals (Sweden)

    Samardžija-Jovanović Suzana

    2005-01-01

    Full Text Available In the process of macromolecule cross linking, the choice of type and quantity of the components and the experimental conditions are important to obtain the new cross linked materials with better mechanical and chemical characteristics. The cross linking method depends on the rubber type and structure. Intermolecular cross linking results in the formation elastomer network. The basis of the cross linking process, between ethylene propylene diene rubber (EPDM and acrylonitrile butadiene rubber (NBR, is a chemical reaction. Fillers and other additives are present in different mass ratios in the material. The exploitation properties of the cross linked materials depend on the quantity of additive in the cross linked systems.

  3. Fatigue Crack Propagation Behavior of Rubber-toughened Epoxy Resin

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Fatigue crack propagation (FCP) behaviors of mass fraction 15% CTBN (carboxyl-terminated butadiene-acrylonitrile), 15% Qishi toughening-agent toughened anhydride-cured epoxy resins (EP), and pure anhydride-cured EP were measured. The results showed that the two main toughening mechanisms, localized shear yielding and void plastics growth, which occurred near the threshold region because the rubber size is much less than the plastics size at the crack front, improved the near threshold FCP behavior and increased the threshold. The stable FCP behavior was obviously improved with the FCP rates decreased to less than 21%.

  4. Preparation of Impact and Weather Resistant Copolymer

    Institute of Scientific and Technical Information of China (English)

    LIANG Tao

    2001-01-01

    @@ Synthesis method of the resin is that crosslinked polybutyl acrylate latex is used as base latex. Styrene (St) and acrylonitrile (AN) are grafted onto polybutyl acrylate latex particle and turn into core-shell copolymer. The resin is a good resin's impact modifier. There are study of influence regularity about additive emulsifier, initiator, monomer concentration, the ratio of St to AN, chain transfer to graft polymerization. A kind of core-shell resin used as impact modifier is obtained. (A) Preparation of Crosslinked Butyl Acrylate Rubber Latex

  5. Preparation of Impact and Weather Resistant Copolymer

    Institute of Scientific and Technical Information of China (English)

    LIANG; Tao

    2001-01-01

    Synthesis method of the resin is that crosslinked polybutyl acrylate latex is used as base latex. Styrene (St) and acrylonitrile (AN) are grafted onto polybutyl acrylate latex particle and turn into core-shell copolymer. The resin is a good resin's impact modifier. There are study of influence regularity about additive emulsifier, initiator, monomer concentration, the ratio of St to AN, chain transfer to graft polymerization. A kind of core-shell resin used as impact modifier is obtained. (A) Preparation of Crosslinked Butyl Acrylate Rubber Latex  ……

  6. Triphenylphosphine-Catalyzed Michael Addition of Alcohols to Acrylic Compounds

    Institute of Scientific and Technical Information of China (English)

    LIU, Hai-Ling; JIANG, Huan-Feng; WANG, Yu-Gang

    2007-01-01

    A facile triphenylphosphine-catalyzed Michael addition of alcohols to acrylic compounds was described. The reaction was carried out in open air at refluxing temperature in the presence of 10 mol% PPh3. Michael addition of saturated and unsaturated alcohols to acrylonitrile or acrylates has been examined. The reaction gaveβ-alkoxy derivatives with isolated yields of 5%-79%. PPh3 is cheaper and more stable than those trialkylphosphines previously used for the similar reactions, and the products can be easily separated from the reaction mixture via distillation.

  7. Crystal structure of 2-(4-chlorophenyl-3-(4-methoxyphenyl-3-(methylsulfanylacrylonitrile

    Directory of Open Access Journals (Sweden)

    Shamantha Kumar

    2014-11-01

    Full Text Available In the title compound, C17H14ClNOS, the aromatic rings are inclined to one another by 64.22 (9°. The acrylonitrile group (C=C—C[triple-bond]N is planar to within 0.003 (2 Å, with the S atom and the methyl C atom displaced from this plane by 0.2317 (6 and −0.637 (2 Å, respectively. In the crystal, molecules are linked via pairs of C—H...π interactions, forming inversion dimers. There are no other significant intermolecular interactions present.

  8. Creation of Robotic Snake to Validate Contact Modeling in Simulation

    Science.gov (United States)

    2013-12-01

    acrylonitrile butadiene styrene (PC-ABS) plastic connected by MX-28 Dynamixel motors. The links were designed so that the robot could be tracked using a...of a series of links designed using SolidWorks CAD software joined together by MX-28 Dynamixel motors (figure 1). The diameter of the links was...chosen so they would be close to the diameter of the original CMU links and still be able to contain the Dynamixel motors being used to drive the snake

  9. Surface Termination of M1 Phase and Rational Design of Propane Ammoxidation Catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Guliants, Vadim

    2015-02-16

    This final report describes major accomplishments in this research project which has demonstrated that the M1 phase is the only crystalline phase required for propane ammoxidation to acrylonitrile and that a surface monolayer terminating the ab planes of the M1 phase is responsible for their activity and selectivity in this reaction. Fundamental studies of the topmost surface chemistry and mechanism of propane ammoxidation over the Mo-V-(Te,Sb)-(Nb,Ta)-O M1 and M2 phases resulted in the development of quantitative understanding of the surface molecular structure – reactivity relationships for this unique catalytic system. These oxides possess unique catalytic properties among mixed metal oxides, because they selectively catalyze three alkane transformation reactions, namely propane ammoxidation to acrylonitrile, propane oxidation to acrylic acid and ethane oxidative dehydrogenation, all of considerable economic significance. Therefore, the larger goal of this research was to expand this catalysis to other alkanes of commercial interest, and more broadly, demonstrate successful approaches to rational design of improved catalysts that can be applied to other selective (amm)oxidation processes.

  10. A Green Platform for Preparation of the Well-Defined Polyacrylonitrile: 60Co γ-ray Irradiation-Initiated RAFT Polymerization at Room Temperature

    Directory of Open Access Journals (Sweden)

    Shuangshuang Zhang

    2017-01-01

    Full Text Available 60Co γ-ray irradiation-initiated reversible addition–fragmentation chain transfer (RAFT polymerization at room temperature with 2-cyanoprop-2-yl 1-dithionaphthalate (CPDN as the chain transfer agent was first applied to acrylonitrile (AN polymerization, providing a “green” platform for preparing polyacrylonitrile (PAN-based carbon fibers using an environment-friendly energy source. Various effects of dose rate, molar ratio of the monomer to the chain transfer agent, monomer concentration and reaction time on the AN polymerization behaviors were performed to improve the controllability of molecular the weight and molecular weight distribution of the obtained PAN. The feature of the controlled polymerization was proven by the first-order kinetics, linear increase of the molecular weight with the monomer conversion and a successful chain-extension experiment. The molecular weight and molecular weight distribution of PAN were characterized by size exclusion chromatography (SEC. 1H NMR and Matrix assisted laser desorption ionization/time of flight mass spectra (MALDI-TOF-MS confirmed the chain-end functionality of PAN, which also was supported by the successful chain-extension experiments of original PANs with acrylonitrile and styrene as the second monomers respectively.

  11. Experimental toxicology of pyrolysis and combustion hazards.

    Science.gov (United States)

    Cornish, H H; Hahn, K J; Barth, M L

    1975-06-01

    Data are presented on the acute toxicity (mortality only) of the thermal degradation products of polymers obtained by two methods of degradation. One system utilized a slowly increasing temperature (5 degrees C/min) and gradual degradation of the polymer with the rats being exposed to degradation products as they were evolved. In this system the more toxic polymers included wool, polypropylene, poly(vinyl chloride), and urethane foam. The second system utilized conditions of rapid combustion and exposure of rats to the total products of combustion for a period of 4 hr. In this system the more toxic materials included red oak, cotton, acrylonitrile-butadiene-styrene (ABS), and styrene-acrylonitrile. It is of interest to note that the natural product wool is among the least toxic under these rapid combustion conditions and among the most toxic under slow pyrolysis conditions. Other materials also vary in the comparative toxicity of their thermal degradation products, depending upon the conditions of degradation and animal exposure. The two experimental techniques presented here may well represent the two extreme conditions of rapid combustion versus slow pyrolysis. Intermediate types of fire situations might be expected to result in relative acute toxicities somewhere between these two extremes. This report deals with acute toxicity on the basis of mortality data only and does not include other parameters of toxicity such as organ weights and histopathology.

  12. Quasi-solid state dye-sensitized solar cells based on pyridine or imidazole containing copolymer chemically crosslinked gel electrolytes

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Quasi-solid state dye-sensitized solar cells based on chemically crosslinking with backbone polymers of poly(vinylpyridine-co-acrylonitrile) (P(VP-co-AN)) or poly(vinylimidazole-co-acrylonitrile) (P(VIM-co- AN)) and diiodide compounds of I(CH2)6I or I(CH2CH2O)nCH2CH2I solidified EC/PC/KI/I2 gel electrolytes have been fabricated. The ionic conductivities and apparent diffusion coefficients of I3-Of the electrolytes and cell performances have been investigated. Providing chemically crosslinking points, pyridine or imidazole from the backbone polymers benefited the open circuit voltage and fill factor of the cells. Consequently, the overall energy conversion efficiencies of the quasi-solid DSSCs improved over 10% even near 20% from that of the liquid electrolyte before solidification. Besides, the employing of crosslinker I(CH2CH2O)nCH2CH2I showed higher electrolytic and cell characters than that of I(CH2)6I.

  13. Pollution characteristics and health risk assessment of volatile organic compounds emitted from different plastic solid waste recycling workshops.

    Science.gov (United States)

    He, Zhigui; Li, Guiying; Chen, Jiangyao; Huang, Yong; An, Taicheng; Zhang, Chaosheng

    2015-04-01

    The pollution profiles of volatile organic compounds (VOCs) emitted from different recycling workshops processing different types of plastic solid waste (PSW) and their health risks were investigated. A total of 64 VOCs including alkanes, alkenes, monoaromatics, oxygenated VOCs (OVOCs), chlorinated VOCs (ClVOCs) and acrylonitrile during the melting extrusion procedure were identified and quantified. The highest concentration of total VOCs (TVOC) occurred in the poly(acrylonitrile-butadiene styrene) (ABS) recycling workshop, followed by the polystyrene (PS), polypropylene (PP), polyamide (PA), polyvinyl chloride (PVC), polyethylene (PE) and polycarbonate (PC) workshops. Monoaromatics were found as the major component emitted from the ABS and PS recycling workshops, while alkanes were mainly emitted from the PE and PP recycling processes, and OVOCs from the PVC and PA recycling workshops. According to the occupational exposure limits' (OEL) assessment, the workers suffered acute and chronic health risks in the ABS and PS recycling workshops. Meanwhile, it was found that most VOCs in the indoor microenvironments were originated from the melting extrusion process, while the highest TVOC concentration was observed in the PS rather than in the ABS recycling workshop. Non-cancer hazard indices (HIs) of all individual VOCs were <1.0, whereas the total HI in the PS recycling workshop was 1.9, posing an adverse chronic health threat. Lifetime cancer risk assessment suggested that the residents also suffered from definite cancer risk in the PS, PA, ABS and PVC recycling workshops.

  14. Novel Poly(imide dioxime) Sorbents: Development and testing for enhanced extraction of uranium from natural seawater

    Energy Technology Data Exchange (ETDEWEB)

    Das, Sadananda; Brown, Suree S.; Mayes, Richard T.; Janke, Christopher J.; Tsouris, Costas; Kuo, Li-Jung; Gill, Gary A.; Dai, Sheng

    2016-04-09

    A new series of amidoxime-based polymer adsorbents were synthesized at the Oak Ridge National Laboratory (ORNL) by electron beam induced grafting of acrylonitrile and itaconic acid onto polyethylene fiber. Hydroxylamine derivatives of poly(acrylonitrile) (PAN) moiety are demonstrated to possess two kinds of functional groups: open-chain amidoxime and cyclic imide dioxime. The open-chain amidoxime is shown to convert to imide dioxime on heat treatment in the presence of an aprotic solvent, like dimethylsulfoxide (DMSO). The formation of amidoxime and imide dioxime was confirmed by 13-C CPMAS spectra. The adsorbents were evaluated for uranium adsorption efficiency at ORNL with simulated seawater spiked with 8 ppm uranium and 5 gallon seawater in a batch reactor, and in flow-through columns with natural seawater at the Marine Science Laboratory (MSL) of Pacific Northwest National Laboratory (PNNL) at Sequim Bay, WA. The DMSO-heat-treated sorbents adsorbed uranium as high as 4.48 g-U/kg-ads. from seawater. Experimental evidence is presented that the poly(imide dioxime) is primarily responsible for enhanced uranium adsorption capacity from natural seawater. The conjugated system in the imide dioxime ligand possesses increased electron donation ability, which is believed to significantly enhance the uranyl coordination in seawater

  15. COORDINATION CROSSLINKING OF NITRILE RUBBER FILLED WITH COPPER SULFATE PARTICLES

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    By incorporating copper sulfate (CuSO4) particles into acrylonitrile butadiene rubber (NBR) followed by heat pressing.a novel vulcanization method is developed in rubber through the formation of coordination crosslinking.This method totally differs from traditional covalent or non-covalent vulcanization approaches of rubber.No other vulcanizing agent or additional additive is involved in this process.By analyzing the results of DMA,XPS and FT-IR,it is found that the crosslinking of CuSO4 particles filled NBR was induced by in situ coordination between nitrogen atoms of nitrile groups (-CN) and copper ions (Cu2+) from CuSO4.SEM and EDX results revealed the generation of a core (CuSO4 solid particle) shell (adherent NBR) structure,which leads to a result that the crosslinked rubber has excellent mechanical properties.Moreover,poly (vinyl chloride)(PVC) and liquid acrylonitrile-butadiene rubber (LNBR) were used as mobilizer to improve the coordination crosslinking of CuSO4/NBR.The addition of PVC or LNBR could lead to higher crosslink density and better mechanical properties of coordination vulcanization.In addition,crystal water in CuSO4 played a positive role to coordination crosslinking of rubber because it decreased the metal point of CuSO4 and promoted the metal ionization.

  16. Graphene networks with low percolation threshold in ABS nanocomposites: selective localization and electrical and rheological properties.

    Science.gov (United States)

    Gao, Chong; Zhang, Shimin; Wang, Feng; Wen, Bin; Han, Chunchun; Ding, Yanfen; Yang, Mingshu

    2014-08-13

    Acrylonitrile-butadiene-styrene resin (ABS)/graphene nanocomposites were prepared through a facile coagulation method. Because the chemical reduction of graphene oxide was in situ conducted in the presence of ABS at the dispersion stage, the aggregation of the graphene nanosheets was avoided. It was shown by transmission electron microscopy that the graphene nanosheets were selectively located and homogeneously dispersed in the styrene-acrylonitrile (SAN) phase. The electrical conductivity and linear viscoelastic behavior of the nanocomposites were systematically studied. With increasing filler content, graphene networks were established in the SAN phase. Consequently, the nanocomposites underwent a transition from electrical insulator to conductor at a percolation threshold of 0.13 vol %, which is smaller than that of other ABS composites. Such a low percolation threshold results from extreme geometry, selective localization, and homogeneous dispersion of the graphene nanosheets in SAN phase. Similarly, the rheological response of the nanocomposites also showed a transition to solid-like behavior. Due to the thermal reduction of graphene nanosheets and structure improvement of graphene networks, enhanced electrical conductivity of the nanocomposites was obtained after annealing.

  17. Improved synthesis of seven aromatic Baylis-Hillman adducts (BHA): evaluation against Artemia salina Leach. and Leishmania chagasi.

    Science.gov (United States)

    Barbosa, Ticiano P; Junior, Cláudio G L; Silva, Fábio P L; Lopes, Horacimone M; Figueiredo, Lucas R F; Sousa, Suervy C O; Batista, Guilherme N; da Silva, Thiago G; Silva, Tania M S; de Oliveira, Márcia R; Vasconcellos, Mário L A A

    2009-04-01

    We described a very efficient procedure to prepare seven aromatic compounds (1-7), a new class of antileishmanial substances, through Baylis-Hillman reaction (BHR). With one, all the Baylis-Hillman adducts were prepared in quantitative yields by reaction of the corresponding aromatic aldehydes in acrylonitrile at 0 degrees C in only 10-40min reaction time. We present our results about the toxicities of these compounds evaluated on the microcrustaceous Artemia salina Leach. and against promastigote Leishmania chagasi. All substances evaluated in this work have showed high bioactivity. The 3-hydroxy-2-methylene-3-(4-bromopheny)propanenitrile (4) (LC(50)=30.9 microg/mL on A. salina; IC(50)=25.2 microM on L. chagasi) was the most active compound evaluated on A. salina Leach. and on promastigote L. chagasi. The 2-[hydroxy(pyridin-4-yl)methyl]acrylonitrile (7) (LC(50)=30.9 microg/mL on A. salina Leach.; IC(50)=4.8 microg/mL on L. chagasi) was also a very active substance evaluated in this work on promastigote L. chagasi.

  18. Carcinogenicity and mechanistic insights on the behavior of epoxides and epoxide-forming chemicals.

    Science.gov (United States)

    Melnick, Ronald L

    2002-12-01

    Many epoxides and their precursors are high production volume chemicals that have major uses in the polymer industry and as intermediates in the manufacture of other chemicals. Several of these chemicals were demonstrated to be carcinogenic in laboratory animal studies conducted by the Ramazzini Foundation (e.g., vinyl chloride, acrylonitrile, styrene, styrene oxide, and benzene) and by the National Toxicology Program (e.g., ethylene oxide, 1,3-butadiene, isoprene, chloroprene, acrylonitrile, glycidol, and benzene). The most common sites of tumor induction were lung, liver, harderian gland, and circulatory system in mice; Zymbal's gland and brain in rats; and mammary gland and forestomach in both species. Differences in cancer outcome among studies of epoxide chemicals may be related to differences in study design (e.g., dose, duration, and route of exposure; observation period; animal strains), as well as biological factors affecting target organ dosimetry of the DNA-reactive epoxide (toxicokinetics) and tissue response (toxicodynamics). N7-Alkylguanine, N1-alkyladenine, and cyclic etheno adducts, as well as K-ras and p53 mutations, have been detected in animals and/or workers exposed to several of these chemicals. The classifications of these chemical carcinogens by IARC and NTP are based on animal and human data and results of mechanistic studies. Reducing occupational and environmental exposures to these chemicals will certainly reduce human cancer risks.

  19. Review of the toxicology of styrene.

    Science.gov (United States)

    Bond, J A

    1989-01-01

    Styrene is used in the production of plastics and resins, which include polystyrene resins, acrylonitrile-butadiene-styrene resins, styrene-acrylonitrile resins, styrene-butadiene copolymer resins, styrene-butadiene rubber, and unsaturated polyester resins. In 1985, styrene ranked in the top ten of synthetic organic chemicals produced in the U.S. This review focuses on various aspects of styrene toxicology including acute and chronic toxicity, carcinogenicity, genotoxicity, pharmacokinetics, effects on hepatic and extrahepatic xenobiotic-metabolizing enzymes, pharmacokinetic modeling, and covalent interactions with macromolecules. There appear to be many similarities between the toxicity and metabolism of styrene in rodents and humans. Needed areas of future research on styrene include studies on the molecular dosimetry of styrene in terms of both hemoglobin and DNA adducts. The results of such research should improve our ability to assess the relationship between exposure to styrene and surrogate measures of "effective dose", thereby improving our ability to estimate the effects of low-level human exposures.

  20. Morphology Formation in PC/ABS Blends during Thermal Processing and the Effect of the Viscosity Ratio of Blend Partners

    Directory of Open Access Journals (Sweden)

    Stefanie Bärwinkel

    2016-08-01

    Full Text Available Morphology formation during compounding, as well as injection molding of blends containing 60 wt % polycarbonate (PC and 40 wt % polybutadiene rubber-modified styrene-acrylonitrile copolymers (ABS, has been investigated by transmission electron microscopy (TEM. Profiles of the blend morphology have been recorded in injection-molded specimens and significant morphology gradients observed between their skin and core. A <10 µm thick surface layer with strongly dispersed and elongated nano-scale (streak-like styrene acrylonitrile (SAN phases and well-dispersed, isolated SAN-grafted polybutadiene rubber particles is followed by a 50–150 µm thick skin layer in which polymer morphology is characterized by lamellar SAN/ABS phases. Thickness of these lamellae increases with the distance from the specimen’s surface. In the core of the specimens the SAN-grafted polybutadiene rubber particles are exclusively present within the SAN phases, which exhibit a much coarser and less oriented, dispersed morphology compared to the skin. The effects of the viscosity of the SAN in the PC/ABS blends on phase morphologies and correlations with fracture mechanics in tensile and impact tests were investigated, including scanning electron microscopy (SEM assessment of the fracture surfaces. A model explaining the mechanisms of morphology formation during injection molding of PC/ABS blends is discussed.

  1. SYNTHESIS AND BIOLOGICAL EVALUATION OF 3-AMINO-2-CYANO-5- (SUBSTITUTED AMINO-4-[(UN SUBSTITUTEDPHENYL] THIOPHENES AS ANTI-TUBERCULAR AGENTS

    Directory of Open Access Journals (Sweden)

    Kapupara Pankaj P

    2010-09-01

    Full Text Available Tuberculosis, due to its relentless nature, is now a major public health threat. The concomitant resurgence of TB with the MDR- or XDR-TB and HIV/AIDS pandemic has exposed the frailties of the current drug armatorium. Based on good structural similarity between BM-212, a novel antimycobacterial agent undergoing clinical trials, and diaryl thiophenes, we have designed novel diaryl thiophenes. Alkyl or aryl isothiocyanates were reacted with substituted phenylacetonitrile in the presence of NaH to afforded 3-mercapto-3-(substitutedamino-2- [(unsubstitutedphenyl]acrylonitrile (5a-h. The designed molecules, 3-amino-2-cyano-5-(substitutedamino-4- [(unsubstitutedphenyl]thiophenes (6a-h were synthesized by cyclocondention of 3-mercapto-3-(substitutedamino- 2-[(unsubstitutedphenyl]acrylonitrile (5a-h with chloroacetonitrile in ethanol. All the compounds were screened for their antimycobacterial activity on mycobacterium tuberculosis using H37Rv strain by 1% proportion method. Some of the synthesized compounds exhibited potent antimycobacterial activity with MIC values in the range of 12.5-100 µg/mL.

  2. Simultaneous measurement of N-Acetyl-S-(2-cyanoethyl)-cysteine and N-acetyl-S-(2-hydroxyethyl)-cysteine in human urine by liquid chromatography-tandem mass spectrometry.

    Science.gov (United States)

    Xiaotao, Zhang; Hongwei, Hou; Wei, Xiong; Qingyuan, Hu

    2014-08-01

    Acrylonitrile, possibly carcinogenic to humans, is mainly present in tobacco smoke and undergoes metabolism to form N-acetyl-S-(2-cyanoethyl)-cysteine (CEMA) and N-acetyl-S-(2-hydroxyethyl)-cysteine (HEMA). A method based on the direct dilution to simultaneously identify and quantify CEMA and HEMA in human urine by rapid resolution liquid chromatography-electrospray ionization tandem mass spectrometry (RRLC-MS-MS) was validated for assessing smoking-related acrylonitrile exposure. The recovery rates of the whole analytical procedure were 98.2-106.0% and 97.1-112.7% for HEMA and CEMA, respectively. The linear range of standard solutions was 0.5-100.0 ng/mL for CEMA and was 0.2-40.0 ng/mL for HEMA. RRLC using a small particle size column was combined with a tandem mass spectrometry system, which lowered the detection limit of analytes, reduced the ion suppression of mass and shortened the analysis time. The proposed method was successfully applied for the analysis of 126 urine samples from smokers and nonsmokers.

  3. 顶空-GC/FID测定水中乙醛丙烯腈吡啶

    Institute of Scientific and Technical Information of China (English)

    张琢; 谷宇

    2015-01-01

    We successfully build a standard analytical method for the detection of acetaldehyde, acrylonitrile, and pyridine in water using gas chromatography-flame ionization detector (GC-FID).Three samples with concentration of 0.005 mg/L, 0.05 mg/L and 0.50mg/L were analyzed and showed a high recovery rate between 82%and 98%and a low relative standard deviation from 2.4%to 5.0%. These results confirm that this method has high accuracy, high precision and high reproducibility, which, consequently, is appropriate for detecting and analyzing acetaldehyde, acrylonitrile, and pyridine in water.%建立了顶空-气相色谱-氢火焰离子化检测器(GC-FID)检测水中乙醛丙烯腈吡啶的方法。根据加标浓度为0.005mg/L、0.05mg/L和0.50mg/L,回收率在82-98%之间,相对标准偏差为2.4-5.0%之间的测定结果,说明该方法准确度高、精确性高、重现性良好,符合水质测定乙醛丙烯腈吡啶的分析。

  4. Milestone Report - Complete New Adsorbent Materials for Marine Testing to Demonstrate 4.5 g-U/kg Adsorbent

    Energy Technology Data Exchange (ETDEWEB)

    Janke, Christopher James [ORNL; Das, Sadananda [ORNL; Oyola, Yatsandra [ORNL; Mayes, Richard T. [ORNL; Saito, Tomonori [ORNL; Brown, Suree [ORNL; Gill, Gary [PNNL; Kuo, Li-Jung [PNNL; Wood, Jordana [PNNL

    2014-08-01

    This report describes work on the successful completion of Milestone M2FT-14OR03100115 (8/20/2014) entitled, “Complete new adsorbent materials for marine testing to demonstrate 4.5 g-U/kg adsorbent”. This effort is part of the Seawater Uranium Recovery Program, sponsored by the U.S. Department of Energy, Office of Nuclear Energy, and involved the development of new adsorbent materials at the Oak Ridge National Laboratory (ORNL) and marine testing at the Pacific Northwest National Laboratory (PNNL). ORNL has recently developed two new families of fiber adsorbents that have demonstrated uranium adsorption capacities greater than 4.5 g-U/kg adsorbent after marine testing at PNNL. One adsorbent was synthesized by radiation-induced graft polymerization of itaconic acid and acrylonitrile onto high surface area polyethylene fibers followed by amidoximation and base conditioning. This fiber showed a capacity of 4.6 g-U/kg adsorbent in marine testing at PNNL. The second adsorbent was prepared by atom-transfer radical polymerization of t-butyl acrylate and acrylonitrile onto halide-functionalized round fibers followed by amidoximation and base hydrolysis. This fiber demonstrated uranium adsorption capacity of 5.4 g-U/kg adsorbent in marine testing at PNNL.

  5. A New Astrobiological Model of the Atmosphere of Titan

    Science.gov (United States)

    Willacy, K.; Allen, M.; Yung, Y.

    2016-10-01

    We present results of an investigation into the formation of nitrogen-bearing molecules in the atmosphere of Titan. We extend a previous model to cover the region below the tropopause, so the new model treats the atmosphere from Titan’s surface to an altitude of 1500 km. We consider the effects of condensation and sublimation using a continuous, numerically stable method. This is coupled with parameterized treatments of the sedimentation of the aerosols and their condensates, and the formation of haze particles. These processes affect the abundances of heavier species such as the nitrogen-bearing molecules, but have less effect on the abundances of lighter molecules. Removal of molecules to form aerosols also plays a role in determining the mixing ratios, particularly of HNC, HC3N, and HCN. We find good agreement with the recently detected mixing ratios of C2H5CN, with condensation playing an important role in determining the abundance of this molecule below 500 km. Of particular interest is the chemistry of acrylonitrile (C2H3CN) which has been suggested by Stevenson et al. as a molecule that could form biological membranes in an oxygen-deficient environment. With the inclusion of haze formation, we find good agreement of our model predictions of acrylonitrile with the available observations.

  6. Methods of fiber surface grafting for interphase design and tailored composite response

    Science.gov (United States)

    Arnold, Jesse Judson

    1997-11-01

    The objective of this research was to develop methods of fiber surface grafting for interphase formation, and to experimentally evaluate and model these interphases in order to further elucidate their role in fiber-reinforced composites. Surface modification by sp{60}Co gamma irradiation was used initially to graft acrylic polymers on the surface of ultra-high modulus (UHMPE) fibers. This technique utilized low dose rates and low total doses, and achieved grafting with retention of the exceptional UHMPE properties. The surface properties of the fibers were evaluated using fourier transform infra-red spectroscopy (FTIR), electron spectroscopy for chemical analysis (ESCA), and mechanical tests and dynamic mechanical spectrometry (DMS) of discontinuous fiber composites. Depending on the glass transition temperature, Tg, and chemical structure of the graft, the fiber/matrix adhesion and the interfacial failure mechanism was tailored to provide either enhanced reinforcement or toughening. Using a three-phase block model, the DMS characteristics of the composites were modeled and the reinforcement efficiencies extrapolated as a function of surface treatment. The model successfully predicts the tan delta response of the composite and the appearance of additional loss dispersions associated with the interphase. However, the interactions between the high-energy gamma radiation and the fiber and grafts yield interphases that are difficult to characterize and control. The hydroperoxidation grafting method was subsequently developed, which permitted the grafting of tethered, linear chains by a free radical-type polymerization. Poly(styrene-stat-acrylonitrile) was grafted initially, in which the nitrogen in acrylonitrile was used as a marker to verify grafting and to estimate the grafting efficiency by ESCA analysis. Tapping modesp{TM} atomic force microscopy (TMAFM) images of the grafted fibers revealed a nodular surface topography with dimensions that were correlated to the

  7. Investigating the Impact of Acetone Vapor Smoothing on the Strength and Elongation of Printed ABS Parts

    Science.gov (United States)

    Gao, Harry; Kaweesa, Dorcas V.; Moore, Jacob; Meisel, Nicholas A.

    2017-03-01

    Acetone vapor smoothing is a chemical treatment that "melts" the surface of additively manufactured acrylonitrile butadiene styrene parts. The process fuses layers together and allows them to reform when vapor is removed, resulting in a smooth surface finish. Although commonly used to improve aesthetics, recent work has begun to investigate the effects of vapor smoothing on part strength. Nevertheless, most of this work has failed to take into account the anisotropic nature of printed parts. Prior research has shown that vapor smoothing reduces strength under best-case loading conditions, when the tensile load is parallel with the direction of the layers. In this article, the authors hypothesize that vapor smoothing may increase strength under nonoptimal loading conditions as a result of increased cohesion between layers and a reduction in stress concentrations. They use a design of experiments approach to identify the combined impact of printing and vapor smoothing parameters on part material properties.

  8. Kinetics and mechanism of the oxidation of some substituted aldonitrones by quinolinium chlorochromate in aqueous DMF medium in the absence and presence of oxalic acid

    Directory of Open Access Journals (Sweden)

    GOVINDASAMY RAJARAJAN

    2009-02-01

    Full Text Available The kinetics of the oxidation of aldonitrones (nitrone by quinolinium chlorochromate (QCC was determined in 50 % DMF–water in the absence and presence of oxalic acid in order to study the effect of oxalic acid. It was considered worthwhile to investigate whether it undergoes co-oxidation or just functions as a catalyst in the reaction. The reaction was followed iodometrically. Under the employed experimental conditions, the reaction is first order each with respect to concentration of nitrone, QCC, and oxalic acid and fractional order with respect to H+ concentration. There was no discernible effect with increasing in ionic strength but the rate of oxidation decreased with decreasing dielectric constant of the medium. Addition of MnSO4 had a significant and acrylonitrile no effect on the reaction rate. A mechanism involving protonated nitrone and QCC as the reactive oxidant is proposed. The activation parameters were calculated and are presented.

  9. Synthesis, Characterization and Antimicrobial Activities of Some New Heterocyclic Schiff Bases Derived from Thiocarbohydrazide.

    Science.gov (United States)

    El-Mahdy, Kamelia; El-Kazak, Azza; Abdel-Megid, Mohamed; Seada, Magdyand; Farouk, Osama

    2016-01-01

    The reaction of prazolobenzothienopyrimidine-3-carbaldehyde 1 with thiocarbohydrazide afforded the Schiff's base 3. The latter compound reacted with some electrophilic reagents to give 1,2,4-triazoles 4-6 and 1,2,4-triazines 7-9. Treatment of compound 3 with 2-cyano-3,3-bis(methylthio)acrylonitrile gave the corresponding 5-amino-4-cyano-3-methylthiopyrazole derivative 11. The reaction of pyrazole 11 with carbon disulfide afforded dithioxopyrazolopyrimidine 12. Acylation of compound 11 by using acetic anhydride yielded acetamide 13. On the other hand, the cyclocondensation of pyrazole 11 with acetic anhydride in pyridine yielded pyrazolopyrimidine derivative 14. The reactivity of compound 11 towards formamide and phenylisothiocyanate to give the pyrazolopyrimidines 15 and 16 was studied. The newly synthesized compounds were screened for their antimicrobial activity.

  10. Covalent immobilization of rabbit-antiaflatoxin-antibodies onto the poly-acrylamideacrylonitrile as well as hybrid material UREASIL and developing an optical immunosensor

    Science.gov (United States)

    Slavova, M.; Georgieva-Nikolova, R.; Hristov, H.; Nikolova, M.

    2017-03-01

    The aim of this work is to describe a covalent immobilization of antibodies onto the poly- acrylamide-acrylonitrile or hybrid material UREASIL and creation of optical immunosensor for determination of aflatoxin Bl. For this purpose, mouse-anti-aflatoxin B1 antibodies with oxidized carbohydrate moieties were covalently immobilized on the membranes of polyacrylamide- polyacrylonitrile copolymer, as well as the hybrid material UREASIL. To determine the affinity> binding of the immobilized antibody with afatoxin Bl was used "sandwich" method. Associated with the immobilized antibody sought ingredients interact with a surplus of secondary' signal antibodies. The described method has been developed as a model system, which can easily be applied for the determination of aflatoxins in samples of different origin. To the best of our knowledge, this is the first study to show that in the establishment of biosensor was used hybrid material UREASIL.

  11. A fabrication method of unique Nafion® shapes by painting for ionic polymer-metal composites

    Science.gov (United States)

    Trabia, Sarah; Hwang, Taeseon; Kim, Kwang J.

    2016-08-01

    Ionic polymer-metal composites (IPMC) are useful actuators because of their ability to be fabricated in different shapes and move in various ways. However, producing unique or intricate shapes can be difficult based upon the current fabrication techniques. Presented here is a fabrication method of producing the Nafion® membrane or thin film through a painting method. Using an airbrush, a Nafion water dispersion is sprayed onto an acrylonitrile butadiene styrene surface with a stencil of the desired shape. To verify that this method of fabrication produces a Nafion membrane similar to that which is commercially available, a sample that was made using the painting method and Nafion 117 purchased from DuPont™ were tested for various characteristics and compared. The results show promising similarities. The painted Nafion sample was chemically plated with platinum and compared with a traditional IPMC for its displacement and blocking force capabilities. The painted IPMC sample showed comparable results.

  12. Colour-Difference Measurement Method for Evaluation of Quality of Electrolessly Deposited Copper on Polymer after Laser-Induced Selective Activation

    Science.gov (United States)

    Gedvilas, Mindaugas; Ratautas, Karolis; Kacar, Elif; Stankevičienė, Ina; Jagminienė, Aldona; Norkus, Eugenijus; Li Pira, Nello; Račiukaitis, Gediminas

    2016-03-01

    In this work a novel colour-difference measurement method for the quality evaluation of copper deposited on a polymer is proposed. Laser-induced selective activation (LISA) was performed onto the surface of the polycarbonate/acrylonitrile butadiene styrene (PC/ABS) polymer by using nanosecond laser irradiation. The laser activated PC/ABS polymer was copper plated by using the electroless copper plating (ECP) procedure. The sheet resistance measured by using a four-point probe technique was found to decrease by the power law with the colour-difference of the sample images after LISA and ECP procedures. The percolation theory of the electrical conductivity of the insulator conductor mixture has been adopted in order to explain the experimental results. The new proposed method was used to determine an optimal set of the laser processing parameters for best plating conditions.

  13. Structural and Electrochemical Analysis of PMMA Based Gel Electrolyte Membranes

    Directory of Open Access Journals (Sweden)

    Chithra M. Mathew

    2015-01-01

    Full Text Available New gel polymer electrolytes containing poly(vinylidene chloride-co-acrylonitrile and poly(methyl methacrylate are prepared by solution casting method. With the addition of 60 wt.% of EC to PVdC-AN/PMMA blend, ionic conductivity value 0.398×10-6 S cm−1 has been achieved. XRD and FT-IR studies have been conducted to investigate the structure and complexation in the polymer gel electrolytes. The FT-IR spectra show that the functional groups C=O and C≡N play major role in ion conduction. Thermal stability of the prepared membranes is found to be about 180°C.

  14. Modified and Unmodified Zinc Oxide as Coagent in Elastomer Compounds

    Directory of Open Access Journals (Sweden)

    Kołodziejczak-Radzimska Agnieszka

    2014-09-01

    Full Text Available The aim of this work was to study the activity of unmodified and modified ZnO in the peroxide crosslinking of hydrogenated acrylonitrile-butadiene elastomer (HNBR and ethylene-propylene copolymer (EPM. In the first step, zinc oxide was obtained by emulsion precipitation. Maleic acid was introduced onto the surface of ZnO using an in situ method. The unmodified and modified zinc oxide was characterized using dispersive and morphological analysis, BET surface area analysis, and elemental, spectroscopic and thermal analysis. In the second stage of the research, the ZnO/MA systems were incorporated into the structure of elastomer compounds improving the kinetic and mechanical properties of vulcanizates. The proposed modification method had a favorable effect on the physicochemical properties of the zinc oxide and on the kinetic and mechanical properties of the vulcanizates. This study demonstrated that modification of zinc oxide by maleic acid is a promising technique.

  15. Kinetics and mechanism of oxidation of chloramphenicol by 1-chlorobenzotriazole in acidic medium

    Indian Academy of Sciences (India)

    R C Hiremath; R V Jagadeesh; Puttaswamy; S M Mayanna

    2005-07-01

    Chloramphenicol (CAP) is an antibiotic drug having a wide spectrum of activity. The kinetics of oxidation of chloramphenicol by 1-chlorobenzotriazole (CBT) in HClO4 medium over the temperature range 293-323 K has been investigated. The reaction exhibits first-order kinetics with respect to [CBT]o and zero-order with respect to [CAP]o. The fractional-order dependence of rate on [H+] suggests complex formation between CBT and H+. It fails to induce polymerization of acrylonitrile under the experimental conditions employed. Activation parameters are evaluated. The observed solvent isotope effect indicates the absence of hydride transfer during oxidation. Effects of dielectric constant and ionic strength of the medium on the reaction rate have been studied. Oxidation products are identified. A suitable reaction scheme is proposed and an appropriate rate law is deduced to account for the observed kinetic data.

  16. Rethinking Timber: Investigation into the Use of Waste Macadamia Nut Shells for Additive Manufacturing

    Science.gov (United States)

    Girdis, Jordan; Gaudion, Lauren; Proust, Gwénaëlle; Löschke, Sandra; Dong, Andy

    2017-03-01

    In this article, the feasibility of turning macadamia nutshells, a waste product from the forestry and agricultural industries, into a three-dimensional (3D) printed, innovative, microtimber product is examined by composing a wood plastic feed stock for fusion deposition modeling. Different ratios of micro-ground macadamia nutshells and acrylonitrile butadiene styrene (ABS) plastics were mixed with a binding agent to extrude a range of filaments. By using a commercial 3D printer, these filaments helped to fabricate specimens that were tested in tension and compression. The results show that printed samples of macadamia-nutshell—ABS composites offer a viable alternative to commercially available wood polymer composite filaments. Although they possess similar mechanical properties, they have a lower density, making them suitable for a range of lightweight product applications. The research demonstrates that there are new opportunities for the use of macadamia nutshell filament in additive manufacturing as a result of its enhanced properties compared with traditional wood filaments.

  17. Mechanism of Surface Modification for Sericite

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Surface modification of sericite by wet method was conducted with the addition of 1.0% (w/w) silane. The resulting wetting contact angle and activity ratio of sericite were 130° and 98% respectively.Good pre-evaluation indexes of oil value (40.8%) and dispersivity (14.0 mL) were obtained. When 30% of sericite was filled into acrylonitrile butadiene styrene(ABS) plastic, the bending strength and tensile strength of the composite material were reduced by 7% and 14.3% in comparison to those of pure ABS plastic, while the rigidity was increased by 3 times, and the impact strength and breaking elongation were reduced significantly.The mechanism of surface modification was investigated and the configuration of silane coupling agent on the surface of sericite was given. Infrared (IR) spectroscopic analysis indicates that the adsorption of silane on the surface of sericite belongs to chemical adsorption.

  18. VINYL RADICAL POLYMERIZATION INITIATED WITH CERIC ION AND ETHYL N,N-DIETHYLDITHIOCARBAMYL ACETATE SYSTEM

    Institute of Scientific and Technical Information of China (English)

    XU Shoujun; QIU Kunyuan

    1997-01-01

    Acrylamide polymerization initiated with a redox initiation system consisting of ceric ion and ethyl N, N-diethyldithiocarbamyl acetate (EDCA) has been studied. It was found that the polymerization rate equation is in good agreement with that of a redox initiated polymerization, and the overall activation energy of the polymerization was determined to be 25.2 kJ·mol-1. Accordingly, the system belongs to a redox initiator. The initiation mechanism was proposed based on the end group analysis using FT-IR, UV spectroscopies.Analysis results revealed that the N, N-diethyldithiocarbamyl radical produced from the redox reaction of EDCA with ceric ion can initiate acrylonitrile (AN) polymerization and form the end group on PAN. The resulting PAN was photopolymerized with butyl acrylate (BA) to form PAN-b-PBA block copolymer.

  19. Heat sterilizable solid-propellant development

    Science.gov (United States)

    Kalfayan, S. H.

    1981-01-01

    The binders tested were polyurethanes made from two hydroxy-terminated polybutadienes, R-45 and Butarez HT, one hydroxy-terminated butadiene-acrylonitrile copolymer, Hycar 1300X 17, and a hydroxy-terminated prepolymer, Esterdiol 560, made from the dimerized fatty acid Empol 1010. The isocyanates used most extensively were isophorone diisocyanate (IPDI) and a polymeric diisocyanate, DDI. Stress relaxation was used to examine the chemical changes that took place in the binder when subjected to the sterilization temperatures. The thermal stability of the oxidizer, ammonium perchlorate (AP), was tested by thermogravimetry in the isothermal and nonisothermal modes. The effect of particle size, recrystallization, moisture content, and doping on the heat stability of AP could be evaluated by this method. The volatile degradation products, obtained when AP samples were aged at 135 C for prolonged periods, were analyzed by mass spectroscopy.

  20. THE DURABILITY OF LARGE-SCALE ADDITIVE MANUFACTURING COMPOSITE MOLDS

    Energy Technology Data Exchange (ETDEWEB)

    Post, Brian K [ORNL; Love, Lonnie J [ORNL; Duty, Chad [University of Tennessee (UTK) and Oak Ridge National Laboratory (ORNL); Vaidya, Uday [University of Tennessee, Knoxville (UTK); Pipes, R. Byron [Purdue University; Kunc, Vlastimil [ORNL

    2016-01-01

    Oak Ridge National Laboratory s Big Area Additive Manufacturing (BAAM) technology permits the rapid production of thermoplastic composite molds using a carbon fiber filled Acrylonitrile-Butadiene-Styrene (ABS) thermoplastic. Demonstration tools (i.e. 0.965 m X 0.559 m X 0.152 m) for composite part fabrication have been printed, coated, and finished with a traditional tooling gel. We present validation results demonstrating the stability of thermoplastic printed molds for room temperature Vacuum Assisted Resin Transfer Molding (VARTM) processes. Arkema s Elium thermoplastic resin was investigated with a variety of reinforcement materials. Experimental results include dimensional characterization of the tool surface using laser scanning technique following demolding of 10 parts. Thermoplastic composite molds offer rapid production compared to traditionally built thermoset molds in that near-net deposition allows direct digital production of the net geometry at production rate of 45 kg/hr.

  1. EFFECT OF ORGANOPHILIZATION AND INTERLAMELLAR SILYLATION OF MONTMORILLONITE ON COMPATIBLIZATION OF POLYMER COMPOSITES

    Directory of Open Access Journals (Sweden)

    Mamdouh Abdel Rahim

    2016-12-01

    Full Text Available Sodium montmorillonite (Na-Mt was modified by cetyltriemethylammoniumbromide (CTAB through cation exchange technique followed by grafting with 3-aminopropyltriethoxysilane (APT. The effects of organophillic surface treatments of montmorillonite on compatibilization of natural rubber (NR /acrylonitrile butadiene rubber (NBR blends was investigated. Physico-mechanical properties of rubber nanocomposites compatibilized with organomodified montmorillonite revealed strong nanocomposite with high tensile properties, impact strength and good resistance to flex fatigue, abrasion and compression set. Dynamic mechanical thermal analysis (DMTA revealed a marked increase in storage modulus (E' and lesser damping characteristics of organically modified clay mineral polymer nanocomposites (CPN due to intercalation of organophilic montmorillonite by rubber matrix. The morphology of the blends became homogeneous and smoother with the presence of exofoliated/intercalated organically modified montmorillonite. Organomodified layered silicate sheets of montmorillonite greatly enhanced barrier properties by creating tortuous path that retarded the progress of solvent molecules through rubber matrix.

  2. OPTIMIZATION STUDY IN MANUFACTURING PROCESS FOR PC/ABS BLENDS

    Institute of Scientific and Technical Information of China (English)

    Huang Chenghung; Fung Chinping; Chang Shihhsing; Hwang Jiunren; Doong Jiliang

    2003-01-01

    The optimization of injection molding process for polycarbonate/acrylonitrile-butadiene-styrene (PC/ABS) blends is studied using Taguchi method and principal component analysis (PCA). Four controllable process factors are studied at three levels each in the manufacturing process. The L9 orthogonal array is conducted to determine the optimum process factor/level combination for single quality of mechanical properties. In addition, the principal component analysis is employed to transform the correlated mechanical properties to a set of uncorrelated components and to evaluate a comprehensive index for multi-response cases. Then the optimum process factor/level combination for multiple qualities can be determined. Finally, the analysis of variance is used to find out the most influential injection molding parameter for single and multiple qualities problems.

  3. Energetics and Compatibility of Plasticizers in Composite Solid Propellants

    Directory of Open Access Journals (Sweden)

    Rm. Muthiah

    1989-04-01

    Full Text Available In this paper a comparative analysis on the energetics of ester type plasticizers such as dioctyl adipate (DOA, dioctyl phthalate (DOP,dibutyl sebacate (DBS, isodecyl pelargonate (IDP, trioctylphosphate (TOF, diethyl phthalate (DEP, tricresyl phosphate (TCPand dibutyl phthalate (DBP and hydrocarbon type plasticizers such as polybutene (PB, spindle oil, naphthenic oil, polymer extender oil(PEO and poly isobutylene (PIB and the impact of some of the plasticizers on the work ability, pot life and mechanical properties of propellants based on two selected polymeric binders namely polybutadiene-acrylic acid-acrylonitrile (PBAN ter polymer andhydroxyl terminated polybutadiene (HTPB have been reported. The compatibility of all the plasticizers on HTPB binder was also studied at different concentration levels and temperatures using Brookfield viscometer and reported. The mechanism of plasticization is also reviewed.

  4. Effect of the structure of ethylene-propylene-diene-graft-polystyrene graft copolymers on morphology and mechanical properties of SAN/EPDM blends

    Directory of Open Access Journals (Sweden)

    2007-03-01

    Full Text Available Ethylene-propylene-diene-graft-polystyrene (EPDM-g-PS copolymers were synthesized to obtain different structures of graft copolymers with different graft lengths and graft densities. The structure of synthesized EPDM-g-PS copolymers was characterized by gel permeation chromatography (GPC and by Fourier transforms infrared spectroscopy (FTIR. These presynthesized graft copolymers were added (5 phr to styrene-acrylonitrile (SAN and ethylene-propylene-diene (EPDM blends, prepared to maintain the following SAN/EPDM ratios a 95/5 and b 90/10. SAN/EPDM blends were characterized by the determination of mechanical properties (tensile strength, elongation at break while their morphology was inspected by scanning electronic microscopy, SEM. The obtained results show that various structures of EPDM-g-PS copolymers influence the miscibility in SAN/EPDM blends. Optimal concentration of side branches of graft copolymers provide the finest morphology and enhance mechanical properties.

  5. Catalytic oxidative conversion of alkanes to olefines and oxygenates

    Energy Technology Data Exchange (ETDEWEB)

    Baerns, M. [Institut fuer Angewandte Chemie Berlin-Adlershof e.V., Berlin (Germany)

    1998-12-31

    All of the direct reaction schemes described and the corresponding process schemes are still in an exploratory state. Ethylene by oxidative coupling of methane could become competitive if process schemes are developed with significantly less expenditures for separation of the product from unconverted feed. No encouragement for formaldehyde from methane can be presently derived from the existing knowledge. Liquid-phase oxidation of methane to methanol appears to be attractive but no final judgement is possible at present. Oxidative dehydrogenation of ethylene and propane look promising although further catalyst improvement is required. Acetic acid from ethane and acrylonitrile from propane have a certain potential as an alternative to present technology. The outlook for acrolein and acrylic acid from propane is less favourable; new concepts for catalyst design are necessary. (orig.)

  6. 回收ABS增韧研究%Study on Toughening of Recycled ABS

    Institute of Scientific and Technical Information of China (English)

    戴伟民

    2011-01-01

    Acrylonitrile-butadiene-styrene (ABS) high-rubber powder (HRP),SBS and TPU were used to toughen recycled ABS. The results show that the toughening effect of ABS HRP is better than that of TPU and SBS.TPU toughening recycled ABS can keep the other aspects of the mechanical properties of ABS and improve flow properties of ABS.%研究了丙烯腈-丁二烯-苯乙烯共聚物(ABS)高胶粉(HRP)、苯乙烯-丁二烯-苯乙烯共聚物(SBS)、热塑性聚氨酯(TPU)对回收ABS的增韧效果.研究表明,ABS高胶粉的增韧效果最佳,而TPU在增韧回收ABS的同时可保持ABS的其他方面的力学性能并提高其流动性.

  7. Diode laser welding of ABS: Experiments and process modeling

    CERN Document Server

    Ilie, Mariana; Mattei, Simone; Cicala, Eugen; Stoica, Virgil; 10.1016/j.optlastec.2008.10.005

    2010-01-01

    The laser beam weldability of acrylonitrile/butadiene/styrene (ABS) plates is determined by combining both experimental and theoretical aspects. In modeling the process, an optical model is used to determine how the laser beam is attenuated by the first material and to obtain the laser beam profile at the interface. Using this information as the input data to a thermal model, the evolution of the temperature field within the two components can be estimated. The thermal model is based on the first principles of heat transfer and utilizes the temperature variation laws of material properties. Corroborating the numerical results with the experimental results, some important insights concerning the fundamental phenomena that govern the process could be extracted. This approach proved to be an efficient tool in determining the weldability of polimeric materials and assures a significant reduction of time and costs with the experimental exploration.

  8. Friction and wear of HNBR with different fillers under dry rolling and sliding conditions

    Directory of Open Access Journals (Sweden)

    2009-02-01

    Full Text Available Peroxide cured hydrogenated acrylonitrile/butadiene rubber (HNBR compounds with 20 parts per hundred rubber (phr active fillers, such as carbon black (CB, multiwall carbon nanotube (MWCNT and silica were produced and their friction and wear properties under unlubricated rolling and sliding conditions were evaluated. The network-related properties of the HNBR compounds were deduced from dynamic-mechanical thermal analysis (DMTA. The coefficient of friction (COF and the specific wear rate (Ws were determined in different home-made test rigs. The CB and MWCNT containing HNBR compounds exhibited the best resistance to rolling and sliding wear, respectively, among the HNBR systems studied. The worn surfaces were inspected in scanning electron microscope (SEM and the wear mechanisms were analyzed and discussed in respect to the types of wear and fillers.

  9. The use of white-rot fungi as active biofilters

    Energy Technology Data Exchange (ETDEWEB)

    Braun-Luellemann, A.; Johannes, C.; Majcherczyk, A.; Huettermann, A. [Univ. Goettingen (Germany). Forstbotanisches Inst.

    1995-12-31

    White-rot fungi, growing on lignocellulosic substrates, have been successfully used as active organisms in biofilters. Filters using these fungi have a very high biological active surface area, allowing for high degrees of retention, a comparatively low pressure drop, and a high physical stability. The unspecific action of the extracellular enzymes of the white-rot fungi allows for the degradation of a wide variety of substances by the same organism. Degradation of several compounds in the gas phase by the white-rot fungi Trametes versicolor, Pleurotus ostreatus, Bjerkandera adusta, and Phanerochaete chrysosporium was tested. Among the aromatic solvents, styrene was the compound that was most readily degraded, followed by ethylbenzene, xylenes, and toluene. Tetrahydrofuran and dichloromethane were also degraded, whereas dioxane could not be attacked by fungi under the conditions used. Acrylonitrile and aniline were degraded very well, whereas pyridine was resistant to degradation. The process for removing styrene is now in the scaling-up stage.

  10. Synthesis of Gemcitabine-13C, 15N2 and Gemcitabine-13C, 15N2 Metabolites

    Directory of Open Access Journals (Sweden)

    ZHU Cheng-gu;YANG Shao-zu;YAN Sheng-wang;FANG Ning-jing;CAI Ding-long;LI Gang

    2014-02-01

    Full Text Available Homemade urea-13C, 15N2 was used to react with 3-methyl acrylonitrile closure to form cytosine-13C, 15N2 (2,which was protected by trimethylsilylation with BSA and condensed with 2-deoxy-2,2-difluoro-D-erythro-pentofuranose-3,5-dibenzoate-1-methanesulfonate at 120 ℃ to afford blocked gemcitabine-13C, 15N2. Hydrolytic removal of the blocking groups of gemcitabine-13C, 15N2 with NaOH gave gemcitabine-13C, 15N2, and its metabolite was obtained by further hydrolytic deamination of gemcitabine-13C, 15N2. The final products were characterized and detected by HPLC, LC-MS and NMR, and confirmed that the chemical purities were higher than 98%, isotopic abundances were 99% 13C, 98% 15N, and they were suitable for drug metabolism studies.

  11. Adsorption Profile of Basic Dye onto Novel Fabricated Carboxylated Functionalized Co-Polymer Nanofibers

    Directory of Open Access Journals (Sweden)

    Marwa F. Elkady

    2016-04-01

    Full Text Available Acrylonitrile-Styrene co-polymer was prepared by solution polymerization and fabricated into nanofibers using the electrospinning technique. The nanofiber polarization was enhanced through its surface functionalization with carboxylic acid groups by simple chemical modification. The carboxylic groups’ presence was dedicated using the FT-IR technique. SEM showed that the nanofiber attains a uniform and porous structure. The equilibrium and kinetic behaviors of basic violet 14 dye sorption onto the nanofibers were examined. Both Langmuir and Temkin models are capable of expressing the dye sorption process at equilibrium. The intraparticle diffusion and Boyd kinetic models specified that the intraparticle diffusion step was the main decolorization rate controlling the process.

  12. Soundproofing effect of nano particle reinforced polymer composites

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Jae Chul; Hong, Young Sun; Nan, Ri Guang; Ahn, Sung Hoon; Kang, Yeon Jun [Seoul National University, Seoul (Korea, Republic of); Jang, Moon Kyu [LS Cable Ltd., Anyang (Korea, Republic of); Lee, Caroline S. [Hanyang University, Ansan (Korea, Republic of)

    2008-08-15

    In this paper, the effects of soundproofing by polymer and carbon-nanotube (CNT) composites were investigated. The specimens for sound insulation measurement were fabricated with Acrylonitrile Butadiene Styrene (ABS)/CNT composites. Tests showed that sound transmission loss of ABS/CNT 15 vol.% composite was higher by 21.7% (4.1 dB) than that of pure ABS specimen at a frequency of 3400 Hz. It was found that the principal factor influencing the improvement of sound insulations of ABS/CNT composites was increased stiffness by CNT additives. To demonstrate the practical applicability of polymer/CNT composites, tests were conducted for the reduction of operational noise from mechanical relay

  13. Tuning the dispersion of multiwall carbon nanotubes in co-continuous polymer blends: a generic approach

    Energy Technology Data Exchange (ETDEWEB)

    Bose, Suryasarathi; Bhattacharyya, Arup R; Khare, Rupesh A; Kulkarni, Ajit R [Department of Metallurgical Engineering and Materials Science, Indian Institute of Technology Bombay, Powai, Mumbai-400076 (India); Patro, T Umasankar [Chemical Engineering Department, Indian Institute of Technology Bombay, Powai, Mumbai-400076 (India); Sivaraman, P [Naval Materials Research Laboratory, Shil-Badlapur Road, Anand Nagar, Ambernath-421506 (India)], E-mail: arupranjan@iitb.ac.in

    2008-08-20

    Melt-mixed blends of polyamide 6 and acrylonitrile-butadiene-styrene (PA6/ABS) with multiwall carbon nanotubes (MWNTs) were prepared with the intention to develop conducting composites. A generic strategy, namely specific interactions combined with reactive coupling, was adopted to facilitate and to retain the 'network-like' structure of MWNTs during melt-mixing. This was facilitated by the sodium salt of 6-amino hexanoic acid (Na-AHA) and certain phosphonium based modifiers, where it was envisaged that these modifiers would establish specific interactions (either 'cation-{pi}' or '{pi}-{pi}' ) with the '{pi}-electron' clouds of MWNTs, as well as restricting them in the PA6 phase of the blends via reactive coupling. This route eventually led to a remarkable increase in the electrical conductivity and dielectric constant in the blends with MWNTs. Raman, FTIR and TEM investigations further supported these observations.

  14. New trends in biotechnology. Biotechnology no atarashii choryu

    Energy Technology Data Exchange (ETDEWEB)

    Karube, I. (The University of Tokyo, Tokyo (Japan). Research Center for Advanced Science and Technology)

    1993-11-30

    This paper focuses on application of the recent biotechnology and introduces its new trends. What has triggered the boom in the application is when the technology has been applied to medicines in the 1970's. Beginning with insulin and interferon, various fibrinolytic agents including tPA and monoclonals have been put on markets one after another in 1991. Progress in humangenomic analysis has led to implementation of gene therapies and diagnoses using genes on gene diseases. Sweeteners used in a large quantity in the foodstuff field are fructoses made by isomerizing glucose produced by using enzymatic bioreactors. Needless to say about production of amino acid, organic acids, saccharides, antibiotics, steroids, and nucleic acid-based compounds by using enzymatic bioreactors, chemicals including acrylic amide from acrylonitrile, enzyme detergents, and bio-herbicides are available commercially. Progress in the technology is seen in all of the fields, including electronics industry and environmental preservation. 6 refs., 4 figs.

  15. HBS-1: A Modular Child-Size 3D Printed Humanoid

    Directory of Open Access Journals (Sweden)

    Lianjun Wu

    2016-01-01

    Full Text Available An affordable, highly articulated, child-size humanoid robot could potentially be used for various purposes, widening the design space of humanoids for further study. Several findings indicated that normal children and children with autism interact well with humanoids. This paper presents a child-sized humanoid robot (HBS-1 intended primarily for children’s education and rehabilitation. The design approach is based on the design for manufacturing (DFM and the design for assembly (DFA philosophies to realize the robot fully using additive manufacturing. Most parts of the robot are fabricated with acrylonitrile butadiene styrene (ABS using rapid prototyping technology. Servomotors and shape memory alloy actuators are used as actuating mechanisms. The mechanical design, analysis and characterization of the robot are presented in both theoretical and experimental frameworks.

  16. Polymer thin-film transistor based on a high dielectric constant gate insulator

    Institute of Scientific and Technical Information of China (English)

    Lü Wen; Peng Jun-Biao; Yang Kai-Xia; Lan Lin-Feng; Niu Qiao-Li; Cao Yong

    2007-01-01

    In this paper full polymer thin-film transistors (PTFTs) based on Poly (acrylonitrile) (PAN) as the gate dielectric and poly (2-methoxy-5-(2'-ethyl-hexyloxy)-1,4-phenylene-vinylene) (MEH-PPV) as the semiconductor layer were investigated by using different channel width/length ratios. Relatively high dielectric constant of the polymer dielectric layer (6.27) can remarkably reduce the threshold voltage of the transistors to below-3 V. Hole field-effect mobility of MEH-PPV of the PTFTs was about 4.8 × 10-4 cm2/Vs, and on/off current ratio was larger than 102, which was comparable with that of transistors with widely used Poly (4-vinyl phenol) (PVP) or SiO2 as gate dielectrics.

  17. Fast Quantum Molecular Dynamics Simulations of Simple Organic Liquids under Shock Compression

    Science.gov (United States)

    Cawkwell, Marc; Niklasson, Anders; Manner, Virginia; McGrane, Shawn; Dattelbaum, Dana

    2013-06-01

    The responses of liquid formic acid, acrylonitrile, and nitromethane to shock compression have been studied using quantum-based molecular dynamics simulations with the self-consistent tight-binding code LATTE. Microcanonical Born-Oppenheimer trajectories with precise energy conservation were computed without relying on an iterative self-consistent field optimization of the electronic degrees of freedom at each time step via the Fast Quantum Mechanical Molecular Dynamics formalism. The input shock pressures required to initiate chemistry in our simulations agree very well with recent laser- and flyer-plate-driven shock compression experiments. On-the-fly analysis of the electronic structure of the liquids over hundreds of picoseconds after dynamic compression revealed that their reactivity is strongly correlated with the temperature and pressure dependence of their HOMO-LUMO gap.

  18. Investigation of the interfacial bonding in composite propellants. 1,3,5-Trisubstituted isocyanurates as universal bonding agents

    Directory of Open Access Journals (Sweden)

    GORDANA S. USCUMLIC

    2006-05-01

    Full Text Available A series of 1,3,5-trisubstituted isocyanurates (substituents: CH2CH2OH, CH2CH=CH2 and CH2CH2COOH was synthesized according to a modified literature procedure. Experimental investigations included modification of the synthetic procedure in terms of the starting materials, solvents, temperature, isolation techniques, as well as purification and identification of the products. All the synthesized isocyanurates were identified by their melting point and FTIR, 1H NMR and UV spectroscopic data. Fourier transform infrared spectrophotometry was also used to study the interaction between ammonium perchlorate, hydroxyl terminated poly(butadiene, carboxyl terminated poly(butadiene, poly(butadiene-co-acrylonitrile, poly(propylene ether, cyclotrimethylenetrinitramine and the compounds synthesized in this work, which can serve as bonding agents. The results show that tris(2-hydroxyethylisocyanurate is a universal bonding agent for the ammonium perchlorate/carboxyl terminated poly(butadiene/cyclotrimethylenetrinitramine composite propellant system.

  19. Millimeter Wave Spectrum of the Weakly Bound Complex CH2═CHCN·H2O: Structure, Dynamics, and Implications for Astronomical Search.

    Science.gov (United States)

    Calabrese, Camilla; Vigorito, Annalisa; Maris, Assimo; Mariotti, Sergio; Fathi, Pantea; Geppert, Wolf D; Melandri, Sonia

    2015-12-03

    The weakly bound 1:1 complex between acrylonitrile (CH2═CHCN) and water has been characterized spectroscopically in the millimeter wave range (59.6-74.4 GHz) using a Free Jet Absorption Millimeter Wave spectrometer. Precise values of the rotational and quartic centrifugal distortion constants have been obtained from the measured frequencies of the normal and isotopically substituted water moiety (DOH, DOD, H(18)OH). Structural parameters have been estimated from the rotational constants and their differences among isotopologues: the complex has a planar structure with the two subunits held together by a O-H···N (2.331(3) Å) and a C-H···O (2.508(4) Å) interaction. The ab initio intermolecular binding energy, obtained at the counterpoise corrected MP2/aug-cc-pVTZ level of calculation, is De = 24.4 kJ mol(-1).

  20. Synthesis and characterization of poly(styrene-co-methyl methacrylate); Sintese e caracterizacao do poli(estireno-co-metacrilato de metila)

    Energy Technology Data Exchange (ETDEWEB)

    Augustinho, Tiago R.; Abarca, Silvia A.C.; Machado, Ricardo A.F. [Departamento de Engenharia Quimica e Alimentos - Universidade Federal de Santa Catarina - UFSC, Florianopolis, SC (Brazil)

    2011-07-01

    Polystyrene (PS) is nowadays commonly used due its advantages over competitors. PS presents a lower cost when compared with Acrylonitrile Butadiene Styrene (ABS) and with Polyethylene Tere-phthalate (PET), and can be easier processed than polypropylene (PP). At expandable form (EPS), can be used as projective equipment, thermal insulation, floating boards, refrigerators, isothermal, and low cost applications such as packaging and disposable material. Searching for more resistant materials and with a low cost, researches with copolymers materials are being developed. In this study, copolymerization reactions were carried out by suspension polymerization using monomers styrene and methyl methacrylate (MMA) with styrene. Styrene was in the highest percentage in relation to the MMA. The MMA was selected because is a monomer that presents a higher resistance than PS. The copolymerization was confirmed by performing infrared spectroscopy (IR), nuclear magnetic resonance of hydrogen (RMN{sup 1}H), differential scanning calorimetry (DSC) and thermogravimetry (TGA). (author)

  1. Tensile deformation mechanisms of ABS/PMMA/EMA blends

    Science.gov (United States)

    Wang, S. H.; Gao, J.; Lin, S. X.; Zhang, P.; Huang, J.; Xu, L. L.

    2014-08-01

    The tensile deformation mechanisms of acrylonitrile - butadiene - styrene (ABS) / polymethyl methacrylate (PMMA) blends toughened by ethylene methacrylate (EMA) copolymer was investigated by analysing the fracture morphology. ABS/PMMA was blended with EMA copolymer by melt mixing technique using co-rotating twin extruder. Tensile tests show that the elongation at break of ABS/PMMA blends can be efficiently improved with the increase in EMA content. Fracture morphology of ABS/PMMA/EMA blends reveals that the material yield induced by hollowing-out of EMA particles and its propagation into yield zone is the main toughening mechanism. Moreover, the appearance that EMA particles in the central area are given priority to hollowing-out may be related to the skin-core structure of the injection moulded parts caused by the different cooling rate between surface and inside in the process of injection moulding.

  2. Polymer concrete composites for the production of high strength pipe and linings in high temperature corrosive environments

    Science.gov (United States)

    Zeldin, A.; Carciello, N.; Fontana, J.; Kukacka, L.

    High temperature corrosive resistant, non-aqueous polymer concrete composites are described. They comprise about 12 to 20% by weight of a water-insoluble polymer binder polymerized in situ from a liquid monomer mixture consisting essentially of about 40 to 70% by weight of styrene, about 25 to 45% by weight acrylonitrile and about 2.5 to 7.5% by weight acrylamide or methacrylamide and about 1 to 10% by weight of a crosslinking agent. This agent is selected from the group consisting of trimethylolpropane trimethacrylate and divinyl benzene; and about 80 to 88% by weight of an inert inorganic filler system containing silica sand and portland cement, and optionally Fe/sub 2/O/sub 3/ or carbon black or mica. A free radical initiator such as di-tert-butyl peroxide, azobisisobutyronitrile, benzoyl peroxide, lauryl peroxide, other organic peroxides and combinations thereof to initiate crosspolymerization of the monomer mixture in the presence of said inorganic filler.

  3. High temperature chemically resistant polymer concrete

    Science.gov (United States)

    Sugama, T.; Kukacka, L.E.

    High temperature chemically resistant, non-aqueous polymer concrete composites consist of about 12 to 20% by weight of a water-insoluble polymer binder. The binder is polymerized in situ from a liquid vinyl-type monomer or mixture of vinyl containing monomers such as triallylcyanurate, styrene, acrylonitrile, acrylamide, methacrylamide, methyl-methacrylate, trimethylolpropane trimethacrylate and divinyl benzene. About 5 to 40% by weight of a reactive inorganic filler selected from the group consisting of tricalcium silicate and dicalcium silicate and mixtures containing less than 2% free lime, and about 48 to 83% by weight of silica sand/ and a free radical initiator such as di-tert-butyl peroxide, azobisisobutyronitrile, benzoyl peroxide, lauryl peroxide, other orgaic peroxides and combinations to initiate polymerization of the monomer in the presence of the inorganic filers are used.

  4. SUPPRESSION OF CELL ADHESION ON POLYACRYLONITRILE-BASED MEMBRANES BY THE ANCHORING OF PHOSPHOLIPID MOIETIES

    Institute of Scientific and Technical Information of China (English)

    Xiao-jun Huang; Xiao-dan Huang; Ai-fu Che; Zhi-kang Xu; Ke Yao

    2006-01-01

    In this work, the membrane surface of poly(acrylonitrile-co-2-hydroxyethyl methacrylate) (PANCHEMA) waschemically modified by anchoring of phospholipid moieties. The process involved the reaction of hydroxyl groups on the membrane surface with 2-chloro-2-oxo-1,3,2-dioxaphospholane (COP) followed by the ring-opening reaction of COP with trimethylamine. Chemical differences between the original and the modified membranes were characterized by FT-IR and XPS. It was found that the amount of macrophage adhered on the modified membrane surface is substantially lower than that on polyacrylonitrile (PAN) and PANCHEMA membranes under the same condition. The morphological change of the adherent cell is also suppressed by the generation ofphospholipid moieties on the membrane surface.

  5. Preparation of carbon monoliths having tailored pore structure from porous polymer precursors

    Energy Technology Data Exchange (ETDEWEB)

    Lagasse, R.R.

    1993-04-01

    This work concerns preparing tailored porous carbon monoliths by pyrolyzing porous polymer precursors. Prior work in this laboratory (1) demonstrated that a low density (0.05 g/cm{sup 3}), high void fraction (97 vol%) carbon monolith could be prepared by pyrolyzing a porous poly(acrylonitrile) (PAN) precursor. A higher density, more robust carbon material is preferred for certain applications, such as electrodes for electrochemical devices. The present work demonstrates that porous carbon monoliths having mass density of 0.7 g/cm{sup 3} can be prepared from a porous PAN precursor if the pyrolysis is controlled carefully. The macropore structure of the carbon is adjusted by changing the pore structure of the PAN precursor, and the finer scale structure (such as the crystallite size L{sub c}) is adjusted by varying the pyrolysis or heat treatment temperature.

  6. Preparation of carbon monoliths having tailored pore structure from porous polymer precursors

    Energy Technology Data Exchange (ETDEWEB)

    Lagasse, R.R.

    1993-01-01

    This work concerns preparing tailored porous carbon monoliths by pyrolyzing porous polymer precursors. Prior work in this laboratory (1) demonstrated that a low density (0.05 g/cm[sup 3]), high void fraction (97 vol%) carbon monolith could be prepared by pyrolyzing a porous poly(acrylonitrile) (PAN) precursor. A higher density, more robust carbon material is preferred for certain applications, such as electrodes for electrochemical devices. The present work demonstrates that porous carbon monoliths having mass density of 0.7 g/cm[sup 3] can be prepared from a porous PAN precursor if the pyrolysis is controlled carefully. The macropore structure of the carbon is adjusted by changing the pore structure of the PAN precursor, and the finer scale structure (such as the crystallite size L[sub c]) is adjusted by varying the pyrolysis or heat treatment temperature.

  7. Puncture-Healing Thermoplastic Resin Carbon-Fiber-Reinforced Composites

    Science.gov (United States)

    Gordon, Keith L. (Inventor); Siochi, Emilie J. (Inventor); Grimsley, Brian W. (Inventor); Cano, Roberto J. (Inventor); Czabaj, Michael W. (Inventor)

    2015-01-01

    A composite comprising a combination of a self-healing polymer matrix and a carbon fiber reinforcement is described. In one embodiment, the matrix is a polybutadiene graft copolymer matrix, such as polybutadiene graft copolymer comprising poly(butadiene)-graft-poly(methyl acrylate-co-acrylonitrile). A method of fabricating the composite is also described, comprising the steps of manufacturing a pre-impregnated unidirectional carbon fiber preform by wetting a plurality of carbon fibers with a solution, the solution comprising a self-healing polymer and a solvent, and curing the preform. A method of repairing a structure made from the composite of the invention is described. A novel prepreg material used to manufacture the composite of the invention is described.

  8. A low volume 3D-printed temperature-controllable cuvette for UV visible spectroscopy.

    Science.gov (United States)

    Pisaruka, Jelena; Dymond, Marcus K

    2016-10-01

    We report the fabrication of a 3D-printed water-heated cuvette that fits into a standard UV visible spectrophotometer. Full 3D-printable designs are provided and 3D-printing conditions have been optimised to provide options to print the cuvette in either acrylonitrile butadiene styrene or polylactic acid polymers, extending the range of solvents that are compatible with the design. We demonstrate the efficacy of the cuvette by determining the critical micelle concentration of sodium dodecyl sulphate at 40 °C, the molar extinction coefficients of cobalt nitrate and dsDNA and by reproducing the thermochromic UV visible spectrum of a mixture of cobalt chloride, water and propan-2-ol.

  9. Evaluation of 3D printed materials used to print WR10 horn antennas

    Science.gov (United States)

    Köhler, Elof; Rahiminejad, Sofia; Enoksson, Peter

    2016-10-01

    A WR10 waveguide horn antenna is 3D printed with three different materials. The antennas are printed on a fusion deposition modeling delta 3D printer built in house at Chalmers University of Technology. The different plastic materials used are an electrically conductive Acrylonitrile butadiene styrene (ABS), a thermally conductive polylactic acid containing 35% copper, and a tough Amphora polymer containing at least 20% carbon fiber. The antennas are all printed with a 0.25 mm nozzle and 100 μm layer thickness and the software settings are tuned to give maximum quality for each material. The three 3D printed horn antennas are compared when it comes to cost, time and material properties.

  10. ABS和PS—HI在加工过程中的降解研究进展%Research Progress in Degradation of ABS and PS-HI During Processing

    Institute of Scientific and Technical Information of China (English)

    白晓涓

    2012-01-01

    Some studies on the effects of processing cycle and processing temperature as well as accelerated aging on the degradation of acrylonitrile-butadiene-styrene (ABS) copolymer and high impact polystyrene (PS-HI) were introduced to supply information for the people who processed and recycled ABS and PS-HI.%综述了多次加工和加速老化对丙烯腈。丁二烯-苯乙烯共聚物(ABS)和高抗冲聚苯乙烯(PS-HI)性能的影响以及不同加工温度对ABS和PS-HI性能的影响方面的研究进展,为加工、回收ABS和PS-HI提供参考。

  11. Investigating the Influence of Electroplating Layer Thickness on the Tensile Strength for Fused Deposition Processed ABS Thermoplastics

    Directory of Open Access Journals (Sweden)

    S.Kannan

    2014-05-01

    Full Text Available Fused Deposition Modeling (FDM is a kind of Rapid prototyping (RP technique, which allows direct transformation of CAD files into physical models. This paper attempts to identify and study the influence of electroplating layer thickness on the mechanical strength of Acrylonitrile butadiene styrene (ABS samples developed from the FDM process. The study is conducted on the tensile test samples of ABS, built on Stratasys FDM vantage SE machine, and tested under IS specified test conditions. The electroplated samples were also subjected to acetic acid tests and surface roughness measurements to check for proper adhesion of plating. The electroplating thickness adopted was 60, 70 and 80 μm. The electroplated tensile samples indicated an increase in the tensile strength with the corresponding increase in the plating thickness. 60 μm sample exhibited lower ductility and 70, 80 μm samples exhibited enhanced ductility.

  12. Chemical Reaction Route Selection Based on Green Chemical Engineering%基于绿色化工的化学反应路径选择

    Institute of Scientific and Technical Information of China (English)

    何潮洪; 葛挺峰; S.H.Yang; D.W.Edwards

    2004-01-01

    In the preliminary stage of chemical process design, the choice of chemical reaction route is the key design decision, and the concepts of atom utilization and environmental quotient have become extremely useful tools. However, the waste quality such as chemical toxicity and other engineering factors have not been taken into account. Therefore, a synthetic route selection index, Iroute, is proposed to determine the suitability of a chemical route in this paper. Iroute considers the effects of "extended atom economy", material renewability, chemical characteristics and some engineering factors. The extended atom economy concept regards not only the value of the desired product but also the value of byproducts. The methodology by using Iroute to compare different routes is illustrated in case study of cyclohexanone oxime and acrylonitrile manufacture.

  13. EB radiation crosslinking of elastomers [rapid communication

    Science.gov (United States)

    Bik, J.; Głuszewski, W.; Rzymski, W. M.; Zagórski, Z. P.

    2003-06-01

    Radiation-induced crosslinking is proposed as successful alternative to conventional, chemical methods of crosslinking of elastomers. Hydrogenated acrylonitrile-butadiene rubber was irradiated with 10 MeV electron beam to doses up to 300 kGy. Irradiated samples were investigated for the extent of crosslinking and for properties important for understanding of mechanisms. It follows from sol-gel analysis, that for 100 crosslinking acts there are 6-9 acts of chain scission. It is less than expected from the 20% participation of multi-ionization spurs, also in the solid state, as announced during the previous 9th Tihany Conference (Radiat. Phys. Chem. 56 (1999) 559). However, the apparent too low yield of multi-ionization spurs could be explained by partial conversion of scission products into crosslinks of specific trifunctional Y type. Our investigations confirm the usefulness of consideration of different radiation spurs in polymers, as well as in all, low LET irradiated media.

  14. EB radiation crosslinking of elastomers

    Energy Technology Data Exchange (ETDEWEB)

    Bik, J.; Gluszewski, W.; Rzymski, W.M.; Zagorski, Z.P. E-mail: zagorski@ichtj.waw.pl

    2003-06-01

    Radiation-induced crosslinking is proposed as successful alternative to conventional, chemical methods of crosslinking of elastomers. Hydrogenated acrylonitrile-butadiene rubber was irradiated with 10 MeV electron beam to doses up to 300 kGy. Irradiated samples were investigated for the extent of crosslinking and for properties important for understanding of mechanisms. It follows from sol-gel analysis, that for 100 crosslinking acts there are 6-9 acts of chain scission. It is less than expected from the 20% participation of multi-ionization spurs, also in the solid state, as announced during the previous 9th Tihany Conference (Radiat. Phys. Chem. 56 (1999) 559). However, the apparent too low yield of multi-ionization spurs could be explained by partial conversion of scission products into crosslinks of specific trifunctional Y type. Our investigations confirm the usefulness of consideration of different radiation spurs in polymers, as well as in all, low LET irradiated media.

  15. Amine and Titanium (IV Chloride, Boron (III Chloride or Zirconium (IV Chloride-Promoted Baylis-Hillman Reactions

    Directory of Open Access Journals (Sweden)

    Shi-Cong Cui

    2001-10-01

    Full Text Available The Baylis-Hillman reactions of various aryl aldehydes with methyl vinyl ketone at temperatures below -20oC using Lewis acids such as titanium (IV chloride, boron (III chloride or zirconium (IV chloride in the presence of a catalytic amount of selected amines used as a Lewis bases afford the chlorinated compounds 1 as the major product in very high yields. Acrylonitrile can also undergo the same reaction to give the corresponding chlorinated product in moderate yield. A plausible reaction mechanism is proposed. However, if the reaction was carried out at room temperature (ca. 20oC, then the Z-configuration of the elimination product 3, derived from 1, was formed as the major product.

  16. Effect of Reprocessing and Accelerated Weathering on Impact-Modified Recycled Blend

    Science.gov (United States)

    Ramesh, V.; Mohanty, Smita; Biswal, Manoranjan; Nayak, Sanjay K.

    2015-12-01

    Recovery of recycled polycarbonate, acrylonitrile butadiene styrene, high-impact polystyrene, and its blends from waste electrical and electronic equipment plastics products properties were enhanced by the addition of virgin polycarbonate and impact modifier. The optimized blend formulation was processed through five cycles, at processing temperature, 220-240 °C and accelerated weathering up to 700 h. Moreover, the effect of reprocessing and accelerated weathering in the physical properties of the modified blends was investigated by mechanical, thermal, rheological, and morphological studies. The results show that in each reprocessing cycle, the tensile strength and impact strength decreased significantly and the similar behavior has been observed from accelerated weathering. Subsequently, the viscosity decreases and this decrease becomes the effect of thermal and photo-oxidative degradation. This can be correlated with FTIR analysis.

  17. Does the ion-molecule reaction between HC tbnd CH rad + and HCN lead to CH 2dbnd CH-C tbnd N rad + ? A computational and experimental study of the reverse process

    Science.gov (United States)

    Jobst, Karl J.; Hasan, Syed A.; Terlouw, Johan K.

    2008-01-01

    The title ion-molecule reaction has been proposed to play an important role in interstellar chemistry if it yields acrylonitrile ions CH 2dbnd CH-C tbnd N rad + . This question was probed by examining the formation of HC tbnd CH rad + and HCN from low-energy ions CH 2dbnd CH-C tbnd N rad + and related isomers, using tandem mass spectrometry based experiments (D and 13C labelling) in conjunction with model chemistry calculations (CBS-QB3/APNO). We conclude that the title reaction is a barrierless multistep rearrangement that may not effectively compete with the straightforward formation of stable distonic ions HC dbnd CH-N dbnd CH rad + from HC tbnd CH rad + (ion)-HCN(dipole) encounter complexes.

  18. Updates of CORESTA Recommended Methods after Further Collaborative Studies Carried Out under Both ISO and Health Canada Intense Smoking Regimes

    Directory of Open Access Journals (Sweden)

    Purkis SW

    2014-12-01

    Full Text Available During 2012, three CORESTA Recommended Methods (CRMs (1-3 were updated to include smoke yield and variability data under both ISO (4 and the Canadian Intense (CI (5 smoking regimes. At that time, repeatability and reproducibility data under the CI regime on smoke analytes other than “tar”, nicotine and carbon monoxide (6 and tobacco-specific nitrosamines (TSNAs (7 were not available in the public literature. The subsequent work involved the determination of the mainstream smoke yields of benzo[a]-pyrene, selected volatiles (benzene, toluene, 1,3-butadiene, isoprene, acrylonitrile, and selected carbonyls (acetaldehyde, formaldehyde, propionaldehyde, butyraldehyde, crotonaldehyde, acrolein, acetone and 2-butanone in ten cigarette products followed by statistical analyses according to the ISO protocol (8. This paper provides some additional perspective on the data variability under the ISO and CI smoking regimes not given in the CRMs.

  19. Clarkson airshed study : a scientific approach to improving air quality : addendum to part 2

    Energy Technology Data Exchange (ETDEWEB)

    Edwards, S. [Ontario Ministry of the Environment, Toronto, ON (Canada)

    2009-04-15

    In the second part of the Clarkson Airshed ambient air monitoring program, detectable concentrations of acrolein were occasionally measured at three monitoring stations in south Mississauga. This report focused on the results for acrolein, acrylonitrile and dichloromethane sampling in ambient air in the vicinity of industrial sources near Winston Churchill Boulevard on Royal Windsor Drive only. Detailed information of these sampling conditions were presented in an appendix and the results were discussed in a memorandum. A photograph of volatile organic compounds in ambient air sampling locations in the summer of 2007 in Clarkson. It was concluded that the results from the three sampling locations and the twelve samples, coupled with Phase 2 results, were statistically insufficient to determine the source contributing to the acrolein exceedances. Based upon poor correlation with wind direction, no one particular point source can be attributed to exclusively contributing to the elevated acrolein concentrations measured. 1 tab., 6 figs., 1 appendix.

  20. Electrospinning to Forcespinning™

    Directory of Open Access Journals (Sweden)

    Kamal Sarkar

    2010-11-01

    Full Text Available A new process called Forcespinning™ has been developed to make nanofibers from a wide range of materials. This new method uses centrifugal force, rather than electrostatic force as in the electrospinning process. The Forcespinning™ method uses either solutions or solid materials that are solution or melt spun into nanofibers. Key parameters to control the geometry and morphology of the nanofibers include rotational speed of the spinneret, collection system and temperature. Orifices of the spinneret can have arbitrary geometric shapes to provide corresponding cross-section of nanofibers. The Forcespinning™ method has been successfully used to make nanofibers of poly-ethylene oxide, poly-lactic acid, bismuth, polypropylene, acrylonitrile-butadiene-styrene, polyvinyl pyrrolidone, and polystyrene among others.

  1. Study of processing conditions on properties of ABS and clay organically modified nanocomposites; Estudo das condicoes de processamento nas propriedades de nanocompositos de ABS e argilas organofilicas

    Energy Technology Data Exchange (ETDEWEB)

    Galvan, Danieli; Massucato, Felipe; Bartoli, Julio R., E-mail: bartoli@feq.unicamp.br [Fac. de Engenharia Quimica/Universidade Estadual de Campinas - DTP/FEQ/UNICAMP, Campinas, SP (Brazil); D' Avila, Marcos A. [Fac. de Engenharia Mecanica/Universidade Estadual de Campinas - DEMA/FEM/UNICAMP, Campinas, SP (Brazil); Fernandes, Elizabeth G. [Tezca P and D Celulas Solares, Campinas, SP (Brazil)

    2011-07-01

    Nanocomposites of poly(acrylonitrile-butadiene-styrene) and organically modified montmorillonite clay were prepared by melt intercalation on a co-rotating twin-screw extruder. The independent variables studied were the kind of organoclay (Cloisite 20A and Cloisite 30B) and the screw torque at levels of 45 and 70%. The effect of these variables on the intercalation/exfoliation were accessed by means of the morphological characteristics using X-ray diffraction and the mechanical properties of uniaxial tensile test. The experimental results showed that the incorporation of clay in the polymeric matrix improved the mechanical properties of elastic modulus, yield stress and tensile strength of nanocomposites, being more significant for that containing Cloisite 30B. Torque was also a significant variable for the responses studied. (author)

  2. Effect of surface modification of Grewia optiva fibres on their physicochemical and thermal properties

    Indian Academy of Sciences (India)

    Amar S Singha; Ashvinder K Rana

    2012-12-01

    This paper deals with the surface modification of Grewia optiva fibre through benzoylation and graft copolymerization process. Benzoylation of Grewia optiva fibre has been carried out on mercerized fibre with varying concentrations of benzoyl chloride solution. Graft copolymerization of acrylonitrile (AN) onto Grewia optiva fibre was carried out with ceric ammonium nitrate as the redox initiator in aqueous medium under the influence of microwave radiation. Raw, graft copolymerized and benzoylated fibres were subjected to evaluation of some of their properties like swelling behaviour, moisture absorbance and chemical resistance behaviour. It has been observed that 5% benzoyl chloride treated and graft copolymerized Grewia optiva show more resistance towards moisture, water and chemicals when compared with that of raw fibre. Further morphological, structural changes, thermal stability and crystallinity of raw, graft copolymerized, pretreated and benzoylated fibres have also been studied by SEM, FTIR, TGA and XRD techniques.

  3. Payne effect in NBR nanocomposites with organophilic montmorillonite; Efeito Payne em nanocompositos de NBR com montmorilonita organofilica

    Energy Technology Data Exchange (ETDEWEB)

    Bezerra, Fernando de O. [Instituto Federal de Educacao, Ciencia e Tecnologia do Rio de Janeiro (IFRJ), Campus Realengo, Rio de Janeiro, RJ (Brazil); Nunes, Regina C.R.; Gomes, Ailton S., E-mail: rcnunes@ima.ufrj.br [Universidade Federal do Rio de Janeiro (IMA/UFRJ), RJ (Brazil). Instituto de Macromoleculas Professora Eloisa Mano; Oliveira, Marcia G. [Instituto Nacional de Tecnologia (INT), Rio de Janeiro, RJ (Brazil); Ito, Edson N. [Universidade Federal do Rio Grande do Norte (UFRN), Natal, RN (Brazil)

    2013-07-01

    In this work the Payne effect was evaluated as a measure of the filler-filler and filler-polymer interactions in nanocomposites of organo montmorillonite (MMTorg) on acrylonitrile-butadiene-rubber (NBR) by using the Rubber Process Analyzer – RPA 2000. The nanocomposites of NBR and MMTorg were prepared on a Berstorff two-roll mill and the evaluation of the Payne effect was carried out in unvulcanized pure gum and varying the MMTorg content from 5, 10, 15 and 20 phr. The composition with 5 phr of MMTorg showed the best filler-polymer interaction as a consequence of the smaller amount of agglomerates of the filler in the elastomeric matrix. (author)

  4. Macromolecular peroxo complexes of Vanadium(V) and Molybdenum(VI): Catalytic activities and biochemical relevance

    Indian Academy of Sciences (India)

    Nashreen S Islam; Jeena Jyoti Boruah

    2015-05-01

    Our recent achievements concerning the synthesis and characterization of water soluble peroxo complexes of V(V) and Mo(VI) in macroligand environment, as well as some key features of biological relevance of these compounds, such as their hydrolytic stability, activity with phosphohydrolase enzyme vis-à-vis free peroxovanadium (pV) or peroxomolybdenum (pMo) complexes, and their activity in biomimetic oxidative bromination are presented here. Immobilization of pMo species on insoluble polymer matrices viz., amino acid functionalized Merrifield resins and poly(acrylonitrile) on the other hand, afforded a set of heterogeneous catalysts highly effective in facile organic transformations such as selective oxidation of organic sulfides and oxidative bromination of aromatic substrates by H2O2, at ambient temperature. The methodologies are straightforward, high-yielding, halogen-free and the catalysts afford easy regeneration. Our findings illustrate the various features which make the procedures sustainable and synthetically useful.

  5. 40 CFR Appendix V to Part 266 - Risk Specific Doses (10−5)

    Science.gov (United States)

    2010-07-01

    ...−04 4.5E−02 1,4-Dioxane 123-91-1 1.4E−06 7.1E+00 Epichlorohydrin 106-89-8 1.2E−06 8.3E+00 Ethylene.... Unit risk (m3/μg) RsD (μg/m3) Acrylamide 79-06-1 1.3E−03 7.7E−03 Acrylonitrile 107-13-1 6.8E−05 1.5E−01 Aldrin 309-00-2 4.9E−03 2.0E−03 Aniline 62-53-3 7.4E−06 1.4E+00 Arsenic 7440-38-2 4.3E−03 2.3E−03...

  6. Rethinking Timber: Investigation into the Use of Waste Macadamia Nut Shells for Additive Manufacturing

    Science.gov (United States)

    Girdis, Jordan; Gaudion, Lauren; Proust, Gwénaëlle; Löschke, Sandra; Dong, Andy

    2016-12-01

    In this article, the feasibility of turning macadamia nutshells, a waste product from the forestry and agricultural industries, into a three-dimensional (3D) printed, innovative, microtimber product is examined by composing a wood plastic feed stock for fusion deposition modeling. Different ratios of micro-ground macadamia nutshells and acrylonitrile butadiene styrene (ABS) plastics were mixed with a binding agent to extrude a range of filaments. By using a commercial 3D printer, these filaments helped to fabricate specimens that were tested in tension and compression. The results show that printed samples of macadamia-nutshell—ABS composites offer a viable alternative to commercially available wood polymer composite filaments. Although they possess similar mechanical properties, they have a lower density, making them suitable for a range of lightweight product applications. The research demonstrates that there are new opportunities for the use of macadamia nutshell filament in additive manufacturing as a result of its enhanced properties compared with traditional wood filaments.

  7. Preparation and characterization of chelating fibers based on natural wool for removal of Hg(II), Cu(II) and Co(II) metal ions from aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Monier, M., E-mail: monierchem@yahoo.com [Chemistry Department, Faculty of Science, Mansoura University, 35516 (Egypt); Nawar, N., E-mail: nnawar@mans.edu.eg [Chemistry Department, Faculty of Science, Mansoura University, 35516 (Egypt); Abdel-Latif, D.A. [Chemistry Department, Faculty of Science, Mansoura University, 35516 (Egypt)

    2010-12-15

    The graft copolymerization of acrylonitrile (AN) onto natural wool fibers initiated by KMnO{sub 4} and oxalic acid combined redox initiator system in limited aqueous medium was carried out in heterogeneous media. Moreover, modification of the grafted wool fibers was done by changing the nitrile group (-CN) into cyano-acetic acid {alpha}-amino-acrylic-hydrazide through the reaction with hydrazine hydrate followed by ethylcyanoacetate which eventually produce wool-grafted-poly(cyano-acetic acid {alpha}-amino-acrylic-hydrazide) (wool-g-PCAH) chelating fibers. The application of the modified fibers for metal ion uptake was studied using Hg{sup 2+}, Cu{sup 2+} and Co{sup 2+}. The modified chelating fibers were characterized using FTIR spectroscopy, SEM and X-ray diffraction.

  8. Erosive Burning Study Utilizing Ultrasonic Measurement Techniques

    Science.gov (United States)

    Furfaro, James A.

    2003-01-01

    A 6-segment subscale motor was developed to generate a range of internal environments from which multiple propellants could be characterized for erosive burning. The motor test bed was designed to provide a high Mach number, high mass flux environment. Propellant regression rates were monitored for each segment utilizing ultrasonic measurement techniques. These data were obtained for three propellants RSRM, ETM- 03, and Castor@ IVA, which span two propellant types, PBAN (polybutadiene acrylonitrile) and HTPB (hydroxyl terminated polybutadiene). The characterization of these propellants indicates a remarkably similar erosive burning response to the induced flow environment. Propellant burnrates for each type had a conventional response with respect to pressure up to a bulk flow velocity threshold. Each propellant, however, had a unique threshold at which it would experience an increase in observed propellant burn rate. Above the observed threshold each propellant again demonstrated a similar enhanced burn rate response corresponding to the local flow environment.

  9. Synthesis of N-decyl-1,3-diaminopropanes and its flotation properties on aluminium silicate minerals

    Institute of Scientific and Technical Information of China (English)

    胡岳华; 曹学锋; 李海普; 蒋玉仁; 杜平

    2003-01-01

    N-decyl-1, 3-diaminopropanes (DNs) were synthesized from alkyl-amine acrylonitrile at ambient pressure. With the synthesized DNs as collectors, the flotation of kaolinite, pyrophyllite and illite was conducted and the results were interpreted in terms of the structure-activity relationship. The DNs are found to be more effective collectors than dodecyl amine, exhibiting the highest recovery over a pH range of 4-6. Among the DNs examined, DN12 shows the highest flotation efficiency. The flotation mechanisms were explained in view of the structures of reagents and aluminium silicate minerals. It is demonstrated that DNs can become new selective collectors for reverse floatation to remove aluminium silicate minerals from bauxite.

  10. Reaction of (Ph2N)2Sm(THF)4 with Azobenzene: Synthesis, X-ray Structure and Catalytic Behavior of [(Ph2N)(DME)Sm]2(μ-η2:η2-N2Ph2)2

    Institute of Scientific and Technical Information of China (English)

    袁福根; 刘秀娟; 张勇

    2005-01-01

    Reaction of divalent (Ph2N)2Sm(THF)4 with 1 equiv, of azobenzene in THF and then crystallization of the product in DME-Et2O mixed solvent produced the complex of [(PhEN)(DME)Sm]E(μ-η2:η2-N2Ph2)2 (1) in 65.0% yield. In complex 1, azobenzene molecules were reduced to be dianionic Ph2N22- ligands, bridging two samarium ions in two η2:η2 fashions. One samarium ion was bonded to a DME molecule and a diphenyl amido ligand besides two Ph2N22- ligands. The unusual Ln-η2-arene close interaction was found for the first time for diphenyl amido lanthanides. Complex 1 could catalyze the polymerization of methyl methacrylate and acrylonitrile

  11. A Study on the Influence of Process Parameters on the Viscoelastic Properties of ABS Components Manufactured by FDM Process

    Science.gov (United States)

    Dakshinamurthy, Devika; Gupta, Srinivasa

    2016-06-01

    Fused Deposition Modelling (FDM) is a fast growing Rapid Prototyping (RP) technology due to its ability to build parts having complex geometrical shape in reasonable time period. The quality of built parts depends on many process variables. In this study, the influence of three FDM process parameters namely, slice height, raster angle and raster width on viscoelastic properties of Acrylonitrile Butadiene Styrene (ABS) RP-specimen is studied. Statistically designed experiments have been conducted for finding the optimum process parameter setting for enhancing the storage modulus. Dynamic Mechanical Analysis has been used to understand the viscoelastic properties at various parameter settings. At the optimal parameter setting the storage modulus and loss modulus of the ABS-RP specimen was 1008 and 259.9 MPa respectively. The relative percentage contribution of slice height and raster width on the viscoelastic properties of the FDM-RP components was found to be 55 and 31 % respectively.

  12. On the Strain Rate Sensitivity of Abs and Abs Plus Fused Deposition Modeling Parts

    Science.gov (United States)

    Vairis, A.; Petousis, M.; Vidakis, N.; Savvakis, K.

    2016-09-01

    In this work the effect of strain rate on the tensile strength of fused deposition modeling parts built with Acrylonitrile-butadiene-styrene (ABS) and ABS plus material is presented. ASTM D638-02a specimens were built with ABS and ABS plus and they were tested on a Schenck Trebel Co. tensile test machine at three different test speeds, equal, lower, and higher to the test speed required by the ASTM D638-02a standard. The experimental tensile strength results were compared and evaluated. The fracture surfaces of selected specimens were examined with a scanning electron microscope, to determine failure mode of the filament strands. It was found that, as the test speed increases, specimens develop higher tensile strength and have higher elastic modulus. Specimens tested in the highest speed of the experiment had on average about 10% higher elastic modulus and developed on average about 11% higher tensile strength.

  13. ABS polymer electroless plating through a one-step poly(acrylic acid) covalent grafting.

    Science.gov (United States)

    Garcia, Alexandre; Berthelot, Thomas; Viel, Pascal; Mesnage, Alice; Jégou, Pascale; Nekelson, Fabien; Roussel, Sébastien; Palacin, Serge

    2010-04-01

    A new, efficient, palladium- and chromium-free process for the electroless plating of acrylonitrile-butadiene-styrene (ABS) polymers has been developed. The process is based on the ion-exchange properties of poly(acrylic acid) (PAA) chemically grafted onto ABS via a simple and one-step method that prevents using classical surface conditioning. Hence, ABS electroless plating can be obtained in three steps, namely: (i) the grafting of PAA onto ABS, (ii) the copper Cu(0) seeding of the ABS surface, and (iii) the nickel or copper metallization using commercial-like electroless plating bath. IR, XPS, and SEM were used to characterize each step of the process, and the Cu loading was quantified by atomic absorption spectroscopy. This process successfully compares with the commercial one based on chromic acid etching and palladium-based seed layer, because the final metallic layer showed excellent adhesion with the ABS substrate.

  14. Fabrication of polystyrene/agave particle biocomposites using compression molding technique: evaluation of flammability, biodegradability, mechanical and thermal behaviour

    Indian Academy of Sciences (India)

    A S Singha; Raj K Rana

    2013-12-01

    Polystyrene (PS) composites reinforced with ungrafted and acrylonitrile (AN) grafted agave particles (AgP) have been prepared with 10–30% particle content by weight using compression molding technique. The composite specimens thus prepared were subjected to the evaluation of mechanical, chemical, flammability and biodegradability properties. PS composites with 20% particle loading exhibited optimum mechanical properties. AN grafted AgP/PS composites exhibited higher mechanical strength as compared to ungrafted AgP/PS composites. Further AN grafted AgP/PS composites exhibited better thermal properties and biodegradability as compared to PS matrix. Addition of fire retardant fillers such as magnesium hydroxide Mg(OH)2 and zinc borate lowered burning rate of PS composites considerably. Scanning electron microscopy (SEM) of tensile fracture surfaces of AN grafted AgP/PS composites showed better particle/matrix adhesion.

  15. SIMULATION OF ELECTRICAL FIELD FOR THE FORMATION MECHANISM OF BIRD'S NEST PATTERNED STRUCTURES BY ELECTROSPINNING

    Institute of Scientific and Technical Information of China (English)

    Xiang-yu Ye; Yi-ning Jin; Xiao-jun Huang; Lei Luo; Zhi-kang Xu

    2013-01-01

    In our previous work,it was found that large Bird's Nest patterned nanofibrous membranes can be simply electrospun from chlorinated polypropylene solution doped with an ionic liquid,and a plausible formation mechanism of Bird's Nest patterned architectures was proposed.Here,we use Ansoft Maxwell version 12 software (3D,electrostatic solver) to simulate the electrical field distribution of the electrospirming setup,and to clarify the rationality of proposed formation mechanism.Calculation results clearly show that the introduction of charged nanofibrous bundles would produce a similar patterned electrical field distribution,which definitely confirms the important role of surface residual charges.The proposed mechanism can be well extended to other polymer systems including polystyrene,poly(acrylonitrile-co-acrylic acid) and chitosan/poly(ethvlene oxide).

  16. Biomonitoring of 1,3-butadiene and related compounds

    Energy Technology Data Exchange (ETDEWEB)

    Osterman-Golkar, S. [Stockholm Univ. (Sweden); Bond, J.A. [Chemical Industry Institute of Toxicology, Research Triangle Park, NC (United States)

    1996-10-01

    The 1990 Clean Air Act Amendments list several volatile organic chemicals as hazardous air pollutants, including ethylene oxide, butadiene, styrene, and acrylonitrile. The toxicology of many of these compounds shares several common elements such as carcinogenicity in laboratory animals, genotoxicity of the epoxide intermediates, involvement of cytochrome P450 for metabolic activation (except ethylene oxide), and involvement of at least two enzymes for detoxication of the epoxides (e.g., hydrolysis or conjugation with glutathione). These similarities facilitate research strategies for identifying and developing biomarkers of exposure. This article reviews the current knowledge about biomarkers of butadiene. Butadiene is carcinogenic in mice and rats, which raises concern for potential carcinogenicity in humans. 85 refs., 1 fig., 2 tabs.

  17. JPRS Report Environmental Issues

    Science.gov (United States)

    1990-08-28

    Acrylonitrile ’ - 2.0 0.5 — 2.0 0.5 2 Acetaldehyde 20.0 10.0 2.5 10.0 5.0 1.3 3 Methyl alcohol 1,000.0 500.0 130.0 200.0 100.0 25.0 4 Ammonia 400.04 200.0 51.0...residual tar, which is a carcinogene . Unfortunately, this can be demonstrated only with sophisticated equipment, which we don’t have." Nevertheless...tests of human hair and nails, soil samples, water and food. Simultaneously, they will evaluate the clinico-medical consequences of the exposure to

  18. Study on Reaction of Tolylene Diisocyanate with Polyolefine Polyols

    Institute of Scientific and Technical Information of China (English)

    Zhang; Fa-Ai

    2001-01-01

    Polyurethane(PU) has been used widely. It is produced by polyisocyanate with polyol. There are many polyisocyanates and polyols. For polyols it is mainly concentrated on polyester and polyether, there is any study on polyolefine polyol. The paper mainly discuss it.By using tolylene diisocyanate(TDI,C6H4CH3(NCO)2) to react with hydroxyterminated polybutadiene(HTPB,HO-[-CH2-CH=CH-CH2-]n-OH,Mn=3805,) and hydroxy-terminated poly(butadiene-co-acrylonitrile)(HTBN, HO-[(-CH2-CH=CHCH2-)x-(-CHCN-CH2)y-]n-OH,Mn=2267), various NCO/OH equivalent ratio NCOterminated polyurethane(PU) prepolymers are synthesized.  ……

  19. Study on Reaction of Tolylene Diisocyanate with Polyolefine Polyols

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    @@ Polyurethane(PU) has been used widely. It is produced by polyisocyanate with polyol. There are many polyisocyanates and polyols. For polyols it is mainly concentrated on polyester and polyether, there is any study on polyolefine polyol. The paper mainly discuss it.By using tolylene diisocyanate(TDI,C6H4CH3(NCO)2) to react with hydroxyterminated polybutadiene(HTPB,HO-[-CH2-CH=CH-CH2-]n-OH,Mn=3805,) and hydroxy-terminated poly(butadiene-co-acrylonitrile)(HTBN, HO-[(-CH2-CH=CHCH2-)x-(-CHCN-CH2)y-]n-OH,Mn=2267), various NCO/OH equivalent ratio NCOterminated polyurethane(PU) prepolymers are synthesized.

  20. Correlation analysis of reactivity in the oxidation of methionine by benzimidazolium fluorochromate in different mole fractions of acetic acid–water mixture

    Directory of Open Access Journals (Sweden)

    S. Sheik Mansoor

    2016-09-01

    Full Text Available The kinetics of oxidation of methionine (Met by benzimidazolium fluorochromate (BIFC has been studied in the presence of chloroacetic acid. The reaction is first order with respect to methionine, BIFC and acid. The reaction rate has been determined at different temperatures and activation parameters calculated. With an increase in the mole fraction of acetic acid in its aqueous mixture, the rate increases. The solvent effect has been analyzed using the Kamlet’s multi parametric equation. A correlation of data with the Kamlet–Taft solvatochromic parameters (α, β, π∗ suggests that the specific solute–solvent interactions play a major role in governing the reactivity. The reaction does not induce polymerization of acrylonitrile. A suitable mechanism has been proposed.

  1. Investigation of the Properties of Immobilized Horseradish Peroxidase on Magnetic Particles

    Directory of Open Access Journals (Sweden)

    Ivanov T.

    2008-12-01

    Full Text Available Magnetic particles coated with copolymer of acrylamide and acrylonitrile have been prepared. Those particles were used as a matrix for a covalent binding of peroxidase. The periodic-oxidized enzyme was bound to the matrix by immobilization procedure at 4°C for 18 hours. The immobilized enzyme showed relative activity of 86%. The following results were obtained for pH and optimum temperature of the immobilized enzyme - 7.0 and 30°C, respectively. The analysis of the kinetic parameters of the immobilized enzyme showed values of Vmax - 0.0517 M.10-6/sec and Km - 2.3x10-4 M.

  2. Advances in DCC Process and Catalyst for Propylene Production from Heavy Oils

    Institute of Scientific and Technical Information of China (English)

    Xie Chaogang; Gao Yongcan

    2008-01-01

    Deep Catalytic Cracking (DCC) developed by RIPP (Research Institute of Petroleum Processing),SINOPEC is a catalytic conversion process derived from the FCC process using heavy feedstocks for producing raw materials used in the petrochemical industry,such as ethylene and propylene.It was firstly demonstrated in 1990 and has been commercialized since 1994.Up to now,seven units have been put into production inside and outside China,and many other DCC units are under construction and in the phase of design now.Products of propylene and ethylene from DCCU have been used as feedstock for manufacturing high quality polypropylene,polyethylene and acrylonitrile.Many innovations on technological process,and preparation of catalytic materials used in the DCC process will be presented in this paper.

  3. Design, synthesis, and evaluation of 2 beta-alkenyl penam sulfone acids as inhibitors of beta-lactamases.

    Science.gov (United States)

    Richter, H G; Angehrn, P; Hubschwerlen, C; Kania, M; Page, M G; Specklin, J L; Winkler, F K

    1996-09-13

    A general method for synthesis of 2 beta-alkenyl penam sulfones has been developed. The new compounds inhibited most of the common types of beta-lactamase. The level of activity depended very strongly on the nature of the substituent in the 2 beta-alkenyl group. The inhibited species formed with the beta-lactamase from Citrobacter freundii 1205 was sufficiently stable for X-ray crystallographic studies. These, together with UV absorption spectroscopy and studies of chemical degradation, suggested a novel reaction mechanism for the new inhibitors that might account for their broad spectrum of action. The (Z)-2 beta-acrylonitrile penam sulfone Ro 48-1220 was the most active inhibitor from this class of compound. The inhibitor enhanced the action of, for example, ceftriaxone against a broad selection of organisms producing beta-lactamases. The organisms included strains of Enterobacteriaceae that produce cephalosporinases, which is an exceptional activity for penam sulfones.

  4. Influence of the association of the EVA and NBR on the characteristics of modified bitumen

    Science.gov (United States)

    Bensaada, A.; Soudani, K.; Haddadi, S.; Saoula, S.

    2015-03-01

    Durability and the performance of pavement depend mainly on the characteristics of materials which change over time like all other organic substances. They are subject to significant changes due to environmental conditions during the different phases of use. In the present work we investigated experimentally the influence of the association of ethyl vinyl acetate polymer (EVA) with an industrial waste, acrylonitrile-butadiene rubber (NBR) on the modification of bitumen AC 35-50 and its rheological behavior. The incorporation of NBR and EVA in the bitumen improved its intrinsic characteristics (softening point, penetration and ductility). In addition to improving the characteristics of bituminous binders that will affect the durability of bituminous structures, the environment will be preserved by the recycling of industrial waste.

  5. WATER RESISTANCE OF WOOD - PLASTIC COMPOSITES MADE FROM WASTE MATERIALS RESULTED IN THE FURNITURE MANUFACTURING PROCESS

    Directory of Open Access Journals (Sweden)

    Camelia COŞEREANU

    2014-12-01

    Full Text Available The purpose of this paper is to present innovative wood-plastic composites made from waste materials such as ABS (acrylonitrile butadiene styrene and wood shavings resulted in the furniture manufacturing process. From previous investigations (with regard to physical integrity and compactness of the panels, only mixtures ranging from a ratio of 100% ABS: 0% shavings to 80% ABS: 20% shavings were selected for water resistance testing. Swelling in thickness and water absorption for 2h and 24h were determined for the proposed wood-plastic composites. The results have shown that only a participation of up to 10% of wood shavings in the tested panels conducted to a good performance

  6. A New Approach toward Transition State Spectroscopy

    CERN Document Server

    Prozument, Kirill; Ciuba, Monika A; Muenter, John S; Park, G Barratt; Stanton, John F; Guo, Hua; Wong, Bryan M; Perry, David S; Field, Robert W

    2013-01-01

    Chirped-Pulse millimetre-Wave (CPmmW) rotational spectroscopy provides a new class of information about photolysis transition state(s). Measured intensities in rotational spectra determine species-isomer-vibrational populations, provided that rotational populations can be thermalized. The formation and detection of S0 vinylidene is discussed in the limits of low and high initial rotational excitation. CPmmW spectra of 193 nm photolysis of Vinyl Cyanide (Acrylonitrile) contain J=0-1 transitions in more than 20 vibrational levels of HCN, HNC, but no transitions in vinylidene or highly excited local-bender vibrational levels of acetylene. Reasons for the non-observation of the vinylidene co-product of HCN are discussed.

  7. Designing of epoxy resin systems for cryogenic use

    Science.gov (United States)

    Ueki, T.; Nishijima, S.; Izumi, Y.

    2005-02-01

    The mechanical and thermal properties of several types of epoxy systems were designed based on the chemical structure, network structure and morphology aiming at cryogenic application. In this research di-epoxies or multifunctional epoxies were cured by several kinds of hardeners such as anhydride, amine or phenol and were blended with polycarbonate, carboxyl-terminated butadiene acrylonitrile copolymer or phenoxy. The mechanical properties and thermal properties of these cured epoxies were measured at room and liquid nitrogen temperature. It was found that the two-dimensional network structured linear polymer shows high performance even at cryogenic temperature. It was concluded that the controls of the structures are very important to optimize epoxy systems for cryogenic application.

  8. Impact property enhancement of poly (lactic acid) with different flexible copolymers

    Science.gov (United States)

    Likittanaprasong, N.; Seadan, M.; Suttiruengwong, S.

    2015-07-01

    The objective of this work was to improve the impact property of Poly (lactic acid) (PLA) by blending with different copolymers. Six flexible copolymers, namely, acrylonitrile butadiene styrene (ABS) powder, Biomax, polybutyrate adipate co-terephthalate (PBAT), polyether block amide (PEBAX), ethylene-vinyl acetate (EVA) and ethylene acrylic elastomer (EAE), with loading less than 20wt% were used and compared. The rheological, mechanical and morphological properties of samples were investigated by melt flow index, tensile testing, impact testing and scanning electron microscope (SEM), respectively. It was found that PLA added 20wt% EAE showed the highest impact strength (59.5 kJ/m2), which was 22 times higher than neat PLA. The elongation at break was also increased by 12 folds compared to neat PLA. The SEM images showed good interface and distribution for PLA containing 20wt% EAE, 15 phr Biomax and 20 wt% PEBAX.

  9. Kinetics and mechanism of the oxidation of some neutral and acidic -amino acids by tetrabutylammonium tribromide

    Indian Academy of Sciences (India)

    Raghvendra Shukla; Pradeep K Sharma; Kalyan K Banerji

    2004-03-01

    The oxidation of eleven amino acids by tetrabutylammonium tribromide (TBATB) in aqueous acetic acid results in the formation of the corresponding carbonyl compounds and ammonia. The reaction is first order with respect to TBATB. Michaelis-Menten type kinetics is observed with some of the amino acids while others exhibit second-order dependence. It failed to induce polymerization of acrylonitrile. The effect of solvent composition indicate that the rate of reaction increases with increase in the polarity of the medium. Addition of tetrabutylammonium chloride has no effect on the rate of oxidation. Addition of bromide ion causes decrease in the oxidation rate but only to a limiting value. The reaction is susceptible to both polar and steric effects of the substituents. A suitable mechanism has been proposed.

  10. Kinetics and mechanism of oxidation of aliphatic alcohols by tetrabutylammonium tribromide

    Indian Academy of Sciences (India)

    Manju Baghmar; Pradeep K Sharma

    2001-04-01

    Oxidation of nine primary aliphatic alcohols by tetrabutylammonium tribromide (TBATB) in aqueous acetic acid leads to the formation of the corresponding aldehydes. The reaction is first order with respect to TBATB. Michaelis-Menten type kinetics is observed with respect to alcohols. The reaction failed to induce the polymerization of acrylonitrile. Tetrabutylammonium chloride has no effect on the reaction rate. The proposed reactive oxidizing species is the tribromide ion. The oxidation of [1,1-2H2]ethanol exhibits a substantial kinetic isotope effect. The effect of solvent composition indicates that the rate increases with increase in the polarity of the solvent. The reaction is susceptible to both polar and steric effects of substituents. A mechanism involving transfer of a hydride ion in the ratedetermining step has been proposed.

  11. Preparation of thin film nanofibrous composite NF membrane based on EDC/NHS modified PAN-AA nanofibrous substrate

    Science.gov (United States)

    Yang, Y.; Wang, X.; Hsiao, B. S.

    2016-07-01

    A novel kind of thin-film nanofibrous composite (TFNC) nanofiltration (NF) membranes consisting of a polyamide (PA) barrier layer were successfully fabricated by interfacial polymerization (IFP) based on electrospun double-layer nanofibrous substrates, which have an ultrathin poly (acrylonitrile-co-acrylic acid) (PAN-AA) nanofibrous layer as top layer and a thicker polyacrylonitrile (PAN) nanofiber layer as bottom porous support layer. Immersing PAN/PAN-AA nanofibrous substrates into 1-ethyl-(3-3-dimethylaminopropyl) carbodiimide hydrochloride/N-hydroxysuccinimide (EDC/NHS) aqueous solution and piperazine (PIP) aqueous solution (0.20 wt%) sequentially for a period of time, the carboxyl groups on PAN-AA nanofibers were activated by carbodiimide and then reacted with the amide groups. The as prepared composite membrane has an integrated structure with high rejection rate (98.0%); high permeate flux (40.4 L/m2h) for MgSO4 aqueous solution (2 g/L).

  12. 氢化丁腈橡胶的结构与性能研究%Molecular Structure and Properties of Hydrogenated Nitrile Rubber

    Institute of Scientific and Technical Information of China (English)

    章菊华; 王珍; 张洪雁; 苏正涛

    2011-01-01

    使用红外光谱(IR)、差示扫描量热法(DSC),热失重(TGA)等方法研究氢化丁腈橡胶(HNBR)分子结构与其低温、高温下物理性能之间的关系.研究结果显示,HNBR橡胶在720~730cm-1处具有明显的(CH2)n(n>4)红外特征吸收峰,由此可以鉴别HNBR与丁腈橡胶(NBR);随丙烯腈含量及氢化度的增大,HNBR的初始热分解温度升高;分子结构中丙烯腈含量越大,玻璃化转变温度越高,其硫化胶的拉伸强度和恒定压缩永久变形越大,这与HNBR分子中交替结构单元增多引起的结晶有关.%A relationship of molecular structure and physical properties at low and high temperatures of hydrogenated nitrile rubber (HNBR) was investigated by Infrared (IR) Spectroscopy, Differential Scanning Caloricity (DSC)and Thermo Gravimetric Analysis (TGA). It is shown that HNBR has characteristic peak of the (CH2)n (n>4)in the backbone at 720-730cm-1 for identified HNBR from NBR. The initial decomposition temperature rose with the increase of the acrylonitrile content and hydrogenation. It is also concluded that the higher acrylonitrile content, the higher Tg, tensile strength and compression set of HNBR, which could be attributed to the crystallization caused by more content of repeat units.

  13. The emissions of monoaromatic hydrocarbons from small polymeric toys placed in chocolate food products.

    Science.gov (United States)

    Marć, Mariusz; Formela, Krzysztof; Klein, Marek; Namieśnik, Jacek; Zabiegała, Bożena

    2015-10-15

    The article presents findings on the emissions of selected monoaromatic hydrocarbons from children's toys placed in chocolate food products. The emission test system involved the application of a new type of microscale stationary emission chamber, μ-CTE™ 250. In order to determine the type of the applied polymer in the manufacture of the tested toys, Fourier transform infrared spectroscopy and thermogravimetric analysis coupled with differential scanning calorimetry were used. It was found that the tested toy components or the whole toys (figurines) are made of two main types of polymers: polyamide and acrylonitrile-butadiene-styrene copolymer. Total number of studied small polymeric toys was 52. The average emissions of selected monoaromatic hydrocarbons from studied toys made of polyamide were as follows: benzene: 0.45 ± 0.33 ng/g; toluene: 3.3 ± 2.6 ng/g; ethylbenzene: 1.4 ± 1.4 ng/g; p,m-xylene: 2.5 ± 4.5 ng/g; and styrene: 8.2 ± 9.9 ng/g. In the case of studied toys made of acrylonitrile-butadiene-styrene copolymer the average emissions of benzene, toluene, ethylbeznene, p,m-xylene and styrene were: 0.31 ± 0.29 ng/g; 2.5 ± 1.4 ng/g; 4.6 ± 8.9 ng/g; 1.4 ± 1.1 ng/g; and 36 ± 44 ng/g, respectively.

  14. New phosphine-diamine and phosphine-amino-alcohol tridentate ligands for ruthenium catalysed enantioselective hydrogenation of ketones and a concise lactone synthesis enabled by asymmetric reduction of cyano-ketones

    Directory of Open Access Journals (Sweden)

    Fuentes José A

    2012-12-01

    Full Text Available Abstract Enantioselective hydrogenation of ketones is a key reaction in organic chemistry. In the past, we have attempted to deal with some unsolved challenges in this arena by introducing chiral tridentate phosphine-diamine/Ru catalysts. New catalysts and new applications are presented here, including the synthesis of phosphine-amino-alcohol P,N,OH ligands derived from (R,S-1-amino-2-indanol, (S,S-1-amino-2-indanol and a new chiral P,N,N ligand derived from (R,R-1,2-diphenylethylenediamine. Ruthenium pre-catalysts of type [RuCl2(L(DMSO] were isolated and then examined in the hydrogenation of ketones. While the new P,N,OH ligand based catalysts are poor, the new P,N,N system gives up to 98% e.e. on substrates that do not react at all with most catalysts. A preliminary attempt at realising a new delta lactone synthesis by organocatalytic Michael addition between acetophenone and acrylonitrile, followed by asymmetric hydrogenation of the nitrile functionalised ketone is challenging in part due to the Michael addition chemistry, but also since Noyori pressure hydrogenation catalysts gave massively reduced reactivity relative to their performance for other acetophenone derivatives. The Ru phosphine-diamine system allowed quantitative conversion and around 50% e.e. The product can be converted into a delta lactone by treatment with KOH with complete retention of enantiomeric excess. This approach potentially offers access to this class of chiral molecules in three steps from the extremely cheap building blocks acrylonitrile and methyl-ketones; we encourage researchers to improve on our efforts in this potentially useful but currently flawed process.

  15. Assessment of Exposure to VOCs among Pregnant Women in the National Children’s Study

    Directory of Open Access Journals (Sweden)

    Elizabeth Barksdale Boyle

    2016-03-01

    Full Text Available Epidemiologic studies can measure exposure to volatile organic compounds (VOCs using environmental samples, biomarkers, questionnaires, or observations. These different exposure assessment approaches each have advantages and disadvantages; thus, evaluating relationships is an important consideration. In the National Children’s Vanguard Study from 2009 to 2010, participants completed questionnaires and data collectors observed VOC exposure sources and collected urine samples from 488 third trimester pregnant women at in-person study visits. From urine, we simultaneously quantified 28 VOC metabolites of exposure to acrolein, acrylamide, acrylonitrile, benzene, 1-bromopropane, 1,3-butadiene, carbon disulfide, crotonaldehyde, cyanide, N,N-dimethylformamide, ethylbenzene, ethylene oxide, propylene oxide, styrene, tetrachloroethylene, toluene, trichloroethylene, vinyl chloride, and xylene exposures using ultra high performance liquid chromatography coupled with an electrospray ionization tandem mass spectrometry (UPLC-ESI/MSMS method. Urinary thiocyanate was measured using an ion chromatography coupled with an electrospray ionization tandem mass spectrometry method (IC-ESI/MSMS. We modeled the relationship between urinary VOC metabolite concentrations and sources of VOC exposure. Sources of exposure were assessed by participant report via questionnaire (use of air fresheners, aerosols, paint or varnish, organic solvents, and passive/active smoking and by observations by a trained data collector (presence of scented products in homes. We found several significant (p < 0.01 relationships between the urinary metabolites of VOCs and sources of VOC exposure. Smoking was positively associated with metabolites of the tobacco constituents acrolein, acrylamide, acrylonitrile, 1,3-butadiene, crotonaldehyde, cyanide, ethylene oxide, N,N-dimethylformamide, propylene oxide, styrene, and xylene. Study location was negatively associated with the toluene metabolite

  16. 静态顶空气相色谱法对土壤中乙醛等物质分析及研究%Analysis and Research of the Substances in Soils Such as Acetaldehyde by Static Headspace-Gas Chromatography

    Institute of Scientific and Technical Information of China (English)

    郭艳

    2015-01-01

    In this research, static headspace technology is used for preliminary treatment of soils and a detection and analysis method of determination of acetaldehyde, acrolein, acrylonitrile and pyridine in soils is set up by static headspace–gas chromatography. Under a certain condition of static headspace-gas chromatography, time and temperature for static headspace is optimized and detection limits for determination of acetaldehyde, acrolein, acrylonitrile, and pyridine in soils by static headspace–gas chromatography are identified, with satisfactory separation efect, linear regression equation, precision and accuracy achieved. The results indicate that analysis of the target compounds in soils by headspace-gas chromatography can reduce the loss of the organic matter in soils to be determined and improve sensitivity and accuracy of the experimentalanalysis.%研究用静态顶空技术处理土壤,从而建立了静态顶空-气相色谱(GC-FID)测定土壤中的乙醛、丙烯醛、丙烯腈和吡啶的检测分析方法。在一定的静态顶空和气相色谱条件下,进行了顶空的时间和温度优化,确定了静态顶空气相色谱法测定土壤中乙醛、丙烯醛、丙烯腈和吡啶方法的检出限,并取得了满意的分离效果、线性回归方程、精密度和准确度。结果表明:用顶空气相色谱法处理土壤样品,可以减少土壤中待测有机物的损失,提高实验分析的灵敏度和准确度。

  17. Recycling of mixed plastic waste from electrical and electronic equipment. Added value by compatibilization.

    Science.gov (United States)

    Vazquez, Yamila V; Barbosa, Silvia E

    2016-07-01

    Plastic waste from electrical and electronic equipment (WEEE) grows up exponentially fast in the last two decades. Either consumption increase of technological products, like cellphones or computers, or the short lifetime of this products contributes to this rise generating an accumulation of specific plastic materials such ABS (Acrylonitrile-Butadiene-Styrene), HIPS (High impact Polystyrene), PC (Polycarbonate), among others. All of they can be recycled by themselves. However, to separate them by type is neither easy nor economically viable, then an alternative is recycling them together as a blend. Taking into account that could be a deterioration in final properties, to enhance phase adhesion and add value to a new plastic WEEE blend a compatibilization is needed. In this work, a systematical study of different compatibilizers for blends of HIPS and ABS from WEEE was performed. A screening analysis was carried out by adding two different compatibilizer concentration (2wt% and 20wt%) on a HIPS/ABS physical blend 80/20 proportion from plastic e-waste. Three copolymers were selected as possible compatibilizers by their possible affinity with initial plastic WEEE. A complete characterization of each WEEE was performed and compatibilization efficiency was evaluated by comparing either mechanical or morphological blends aspects. Considering blends analyzed in this work, the best performance was achieved by using 2% of styrene-acrylonitrile rubber, obtaining a compatibilized blend with double ultimate strength and modulus respect to the physical blend, and also improve mechanical properties of initial WEEE plastics. The proposed way is a promise route to improve benefit of e-scrap with sustainable, low costs and easy handling process. Consequently, social recycling interest will be encouraged by both ecological and economical points of view.

  18. Radiation synthesis of a new amidoximated UHMWPE fibrous adsorbent with high adsorption selectivity for uranium over vanadium in simulated seawater

    Science.gov (United States)

    Gao, Qianhong; Hu, Jiangtao; Li, Rong; Xing, Zhe; Xu, Lu; Wang, Mouhua; Guo, Xiaojing; Wu, Guozhong

    2016-05-01

    A new kind of highly efficient adsorbent material has been fabricated in this study for the purpose of extracting uranium from seawater. Ultra-high molecular weight polyethylene (UHMWPE) fiber was used as a trunk material for the adsorbent, which was prepared by a series of modification reactions, as follows: (1) grafting of glycidyl methacrylate (GMA) and methyl acrylate (MA) onto UHMWPE fibers via 60Co γ-ray pre-irradiation; (2) aminolyzation of UHMWPE fiber by the ring-opening reaction between of epoxy groups PGMA and ethylene diamine (EDA); (3) Michael addition of amino groups with acrylonitrile (AN) to yield nitrile groups; (4) amidoximation of the attached nitrile moieties by hydroxylamine in dimethyl sulfoxide-water mixture. Modified UHMWPE fibers were characterized by means of attenuated total reflectance-Fourier transformed infrared spectroscopy (ATR-FTIR), thermogravimetric analysis (TGA) and scanning electron microscopy (SEM) to confirm the attachment of amidoxime (AO) groups onto the UHMWPE fibers. The results of X-ray diffraction (XRD) and single fiber tensile strength verified that the modified UHMWPE fiber retained excellent mechanical properties at a low absorbed radiation dose. The adsorption performance of the UHMWPE fibrous adsorbent was evaluated by subjecting it to an adsorption test in simulated seawater using a continuous-flow mode. The amount of uranium adsorbed by this AO-based UHMWPE fibrous adsorbent was 1.97 mg-U/g after 42 days. This new adsorbent also showed high selectivity for the uranyl ion, and its selectivity for metal ions was found to decrease in the following order: U>Cu>Fe>Ca>Mg>Ni>Zn>Pb>V>Co. The adsorption selectivity for uranium is significantly higher than that for vanadium. In addition, preparation of this modified adsorbent consumes much smaller amounts of the toxic acrylonitrile monomer than the conventional preparation methods of AO-based polyethylene fibers.

  19. Assessment of Exposure to VOCs among Pregnant Women in the National Children’s Study

    Science.gov (United States)

    Boyle, Elizabeth Barksdale; Viet, Susan M.; Wright, David J.; Merrill, Lori S.; Alwis, K. Udeni; Blount, Benjamin C.; Mortensen, Mary E.; Moye, John; Dellarco, Michael

    2016-01-01

    Epidemiologic studies can measure exposure to volatile organic compounds (VOCs) using environmental samples, biomarkers, questionnaires, or observations. These different exposure assessment approaches each have advantages and disadvantages; thus, evaluating relationships is an important consideration. In the National Children’s Vanguard Study from 2009 to 2010, participants completed questionnaires and data collectors observed VOC exposure sources and collected urine samples from 488 third trimester pregnant women at in-person study visits. From urine, we simultaneously quantified 28 VOC metabolites of exposure to acrolein, acrylamide, acrylonitrile, benzene, 1-bromopropane, 1,3-butadiene, carbon disulfide, crotonaldehyde, cyanide, N,N-dimethylformamide, ethylbenzene, ethylene oxide, propylene oxide, styrene, tetrachloroethylene, toluene, trichloroethylene, vinyl chloride, and xylene exposures using ultra high performance liquid chromatography coupled with an electrospray ionization tandem mass spectrometry (UPLC-ESI/MSMS) method. Urinary thiocyanate was measured using an ion chromatography coupled with an electrospray ionization tandem mass spectrometry method (IC-ESI/MSMS). We modeled the relationship between urinary VOC metabolite concentrations and sources of VOC exposure. Sources of exposure were assessed by participant report via questionnaire (use of air fresheners, aerosols, paint or varnish, organic solvents, and passive/active smoking) and by observations by a trained data collector (presence of scented products in homes). We found several significant (p < 0.01) relationships between the urinary metabolites of VOCs and sources of VOC exposure. Smoking was positively associated with metabolites of the tobacco constituents acrolein, acrylamide, acrylonitrile, 1,3-butadiene, crotonaldehyde, cyanide, ethylene oxide, N,N-dimethylformamide, propylene oxide, styrene, and xylene. Study location was negatively associated with the toluene metabolite N

  20. Determination of methyl-, 2-hydroxyethyl- and 2-cyanoethylmercapturic acids as biomarkers of exposure to alkylating agents in cigarette smoke.

    Science.gov (United States)

    Scherer, Gerhard; Urban, Michael; Hagedorn, Heinz-Werner; Serafin, Richard; Feng, Shixia; Kapur, Sunil; Muhammad, Raheema; Jin, Yan; Sarkar, Mohamadi; Roethig, Hans-Juergen

    2010-10-01

    Alkylating agents occur in the environment and are formed endogenously. Tobacco smoke contains a variety of alkylating agents or precursors including, among others, N-nitrosodimethylamine (NDMA), 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), acrylonitrile and ethylene oxide. We developed and validated a method for the simultaneous determination of methylmercapturic acid (MMA, biomarker for methylating agents such as NDMA and NNK), 2-hydroxyethylmercapturic acid (HEMA, biomarker for ethylene oxide) and 2-cyanoethylmercapturic acid (CEMA, biomarker for acrylonitrile) in human urine using deuterated internal standards of each compound. The method involves liquid/liquid extraction of the urine sample, solid phase extraction on anion exchange cartridges, derivatization with pentafluorobenzyl bromide (PFBBr), liquid/liquid extraction of the reaction mixture and LC-MS/MS analysis with positive electrospray ionization. The method was linear in the ranges of 5.00-600, 1.00-50.0 and 1.50-900 ng/ml for MMA, HEMA and CEMA, respectively. The method was applied to two clinical studies in adult smokers of conventional cigarettes who either continued smoking conventional cigarettes, were switched to test cigarettes consisting of either an electrically heated cigarette smoking system (EHCSS) or having a highly activated carbon granule filter that were shown to have reduced exposure to specific smoke constituents, or stopped smoking. Urinary excretion of MMA was found to be unaffected by switching to the test cigarettes or stop smoking. Urinary HEMA excretion decreased by 46 to 54% after switching to test cigarettes and by approximately 74% when stopping smoking. Urinary CEMA excretion decreased by 74-77% when switching to test cigarettes and by approximately 90% when stopping smoking. This validated method for urinary alkylmercapturic acids is suitable to distinguish differences in exposure not only between smokers and nonsmokers but also between smoking of conventional and