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Sample records for butadiene

  1. The reactivity of 1,3-butadiene with butadiene-derived popcorn polymer.

    Science.gov (United States)

    Levin, M E; Hill, A D; Zimmerman, L W; Paxson, T E

    2004-11-11

    Adiabatic calorimetry performed on butadiene-derived popcorn polymer samples from industrial facilities has revealed exothermic behavior accompanied by non-condensible gas production, indicative of possible decomposition, at elevated temperatures. In the presence of low concentrations of 1,3-butadiene, reactivity is observed at temperatures of 60-70 degrees C; that is, 20-30 degrees C below those usually seen for butadiene alone. Once the butadiene is consumed, the reaction behavior reverts to that of the popcorn polymer alone. At higher butadiene concentrations, the low temperature reaction persists, eventually merging with typical butadiene behavior. The butadiene reactivity with popcorn polymer is attributed to polymerization reaction at free radical sites in the popcorn polymer. Different popcorn polymer samples exhibit distinct extents of reactivity, presumably depending on the nature and concentration of the free radical sites and the structure of the material. Uninhibited butadiene exposed to 100 psia air, which may act to generate peroxide species, shows a small, additional exotherm around 50-80 degrees C. Contact of butadiene with lauroyl peroxide, providing free radicals upon decomposition, generates an exotherm at temperatures as low as 60 degrees C.

  2. HEALTH ASSESSMENT OF 1,3-BUTADIENE | Science ...

    Science.gov (United States)

    This assessment was conducted to review the new information that has become available since EPA's 1985 health assessment of 1,3-butadiene.1,3-Butadiene is a gas used commercially in the production of styrene-butadiene rubber, plastics, and thermoplastic resins. The major environmental source of 1,3-butadiene is the incomplete combustion of fuels from mobile sources (e.g., automobile exhaust). Tobacco smoke can be a significant source of 1,3-butadiene in indoor air.This assessment concludes that 1,3-butadiene is carcinogenic to humans by inhalation, based on the total weight of evidence. The specific mechanisms of 1,3-butadiene-induced carcinogenesis are unknown; however, it is virtually certain that the carcinogenic effects are mediated by genotoxic metabolites of 1,3-butadiene.Animal data suggest that females may be more sensitive than males for cancer effects; nevertheless, there are insufficient data from which to draw any conclusions on potentially sensitive subpopulations.The human incremental lifetime unit cancer (incidence) risk estimate is based on extrapolation from leukemias observed in an occupational epidemiologic study. A twofold adjustment to the epidemiologic-based unit cancer risk is then applied to reflect evidence from the rodent bioassays suggesting that the epidemiologic-based estimate may underestimate total cancer risk from 1,3-butadiene exposure in the general population. 1,3-Butadiene also causes a variety of reproductive and develop

  3. 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.

  4. Industrial emissions of 1,3-butadiene.

    Science.gov (United States)

    Mullins, J A

    1990-06-01

    Sources of industrial emissions of 1,3-butadiene are discussed both by process (production, consumers) and type (equipment leaks, point sources). Quantification of the emissions are presented, as reported by the U.S. Environmental Protection Agency in 1986. The reported emissions attributed to equipment leaks (also known as fugitive emissions) range from about 50 to 95% of the total, depending on the specific production process used. The methods by which these emissions were estimated are discussed, with particular emphasis on the fugitive sources. Industry studies to better quantify the fugitive emissions are described.

  5. Health Assessment Document for 1,3-Butadiene (External ...

    Science.gov (United States)

    This risk assessment of 1,3-butadiene, a gas used commercially in the production of various resins and plastics, concludes that 1,3-butadiene is a known human carcinogen, based on three types of evidence: 1) excess leukemias in workers occupationally exposed to 1,3-butadiene (by inhalation), 2) occurrence of a variety of tumors in mice and rats by inhalation, and 3) evidence in animals and humans that 1,3-butadiene is metabolized into genotoxic metabolites. The best estimate of human lifetime extra cancer risk from chronic exposure to 1,3-butadiene is 9 X 10-3 per ppm based on a linear extrapolation of the increased leukemia risks observed in occupationally exposed workers. The corresponding estimate of the chronic exposure level of 1,3-butadiene resulting in an extra cancer risk of 10-6 (i.e., one in a million) is 0.1 ppb.1,3-Butadiene also causes a variety of reproductive and developmental effects in mice and rats; no human data on these effects are available. There are insufficient data from which to draw any conclusions on potentially sensitive subpopulations.

  6. Dynamic response of acrylonitrile butadiene styrene under impact loading

    National Research Council Canada - National Science Library

    Owolabi, Gbadebo; Peterson, Alex; Habtour, Ed; Riddick, Jaret; Coatney, Michael; Olasumboye, Adewale; Bolling, Denzell

    2016-01-01

    ... rateloading.Tensile tests were conducted on 3-D printed acrylonitrile butadiene styrene (ABS) at differentstrain rates, according to the ASTM D638 standard, to assess its strain rate sensitivity under quasi-staticloads...

  7. Modification of PVC compounds with butadiene-acrylonitrile elastomers

    OpenAIRE

    J. Stabik; M. Rojek

    2006-01-01

    Purpose: The purpose of the paper is to present the research programme on influence of acrylonitrile-butadiene copolymers on properties of plasticized polyvinylchloride as window gaskets material.Design/methodology/approach: Short literature review concerning application of modified PVC as gasket material was presented. In experimental part two types of acrylonitrile-butadiene copolymers were used as elastomeric plasticizers. Compounds with fifteen different levels of modifiers content (up to...

  8. Recent Breakthroughs in the Conversion of Ethanol to Butadiene

    Directory of Open Access Journals (Sweden)

    Guillaume Pomalaza

    2016-12-01

    Full Text Available 1,3-Butadiene is traditionally produced as a byproduct of ethylene production from steam crackers. What is unusual is that the alternative production route for this important commodity chemical via ethanol was developed a long time ago, before World War II. Currently, there is a renewed interest in the production of butadiene from biomass due to the general trend to replace oil in the chemical industry. This review describes the recent progress in the production of butadiene from ethanol (ETB by one or two-step process through intermediate production of acetaldehyde with an emphasis on the new catalytic systems. The different catalysts for butadiene production are compared in terms of structure-catalytic performance relationship, highlighting the key issues and requirements for future developments. The main difficulty in this process is that basic, acid and redox properties have to be combined in one single catalyst for the reactions of condensation, dehydration and hydrogenation. Magnesium and zirconium-based catalysts in the form of oxides or recently proposed silicates and zeolites promoted by metals are prevailing for butadiene synthesis with the highest selectivity of 70% at high ethanol conversion. The major challenge for further application of the process is to increase the butadiene productivity and to enhance the catalyst lifetime by suppression of coke deposition with preservation of active sites.

  9. Fluorescence Efficiency of Tetra-Phenyl-Butadiene

    Science.gov (United States)

    Moore, D. A.; Maassen, J.; Gehman, V. M.; Seibert, S.; Hime, A.; Rielage, K.; Mei, D.; Sun, Y.

    2009-10-01

    Tetra-Phenyl-Butadiene (TPB), a known organic wavelength shifter, converts UV scintillation light into visible light detectable by Photomultiplier Tubes (PMTs). Experiments based in liquid argon, such as CLEAN and DEAP require TPB to correct for the sensitivity of the PMTs. The primary objective of these experiments is detecting WIMPs (Weakly Interacting Massive Particles) that may compose the dark matter in the Universe. We systematically investigated the effects of different wavelengths on TPB-coated acrylic disks using a deuterium lamp as a source of UV light, a monochromator, and a calibrated photodiode detector. We tested a variety of thicknesses of TPB on acrylic disks and blank disks to analyze the spectra and shed new light on several properties and attributes of TPB. We examined the emission spectrum of TPB and evaluated the conversion efficiency (photons out / photons in) in order to broaden the knowledge of how to optimize the visible light collection on the PMTs, while aiding in several modeling processes. I will present our findings on the efficiency and spectral emission of TPB, along with images of the actual setup, as well as possible future research.

  10. On the catalytic gas phase oxidation of butadiene to furan

    Energy Technology Data Exchange (ETDEWEB)

    Kubias, B.; Rodemerck, U. [Institut fuer Angewandte Chemie Berlin-Adlershof e.V., Berlin (Germany); Ritschl, F.; Meisel, M. [Humboldt-Universitaet, Berlin (Germany). Inst. fuer Chemie

    1998-12-31

    Applying the thermochemical selectivity criterion of Hadnett et al. It is shown that the selectivity of the furan formation is not limited by a too low strength of the C-H bonds in furan when compared with the C-H bond dissociation energy in the educt molecule butadiene. In the oxidation of butadiene on a CsH{sub 2}PMo{sub 12}O{sub 40} catalyst a maximum yield of 22 mol% furan has been obtained. To improve this comparatively low furan yield oxidation activity of the catalyst must be lowered to prevent the consecutive reaction to maleic anhydride. (orig.)

  11. Investigation of surface halide modification of nitrile butadiene rubber

    Science.gov (United States)

    Sukhareva, K. V.; Mikhailov, I. A.; Andriasyan, Yu O.; Mastalygina, E. E.; Popov, A. A.

    2017-12-01

    The investigation is devoted to the novel technology of surface halide modification of rubber samples based on nitrile butadiene rubber (NBR). 1,1,2-trifluoro-1,2,2-trichlorethane was used as halide modifier. The developed technology is characterized by production stages reduction to one by means of treating the rubber compound with a halide modifier. The surface halide modification of compounds based on nitrile butadiene rubber (NBR) was determined to result in increase of resistance to thermal oxidation and aggressive media. The conducted research revealed the influence of modification time on chemical resistance and physical-mechanical properties of rubbers under investigation.

  12. Gender differences in the metabolism of 1,3-butadiene to butadiene diepoxide in Sprague-Dawley rats

    Energy Technology Data Exchange (ETDEWEB)

    Thornton-Manning, J.R.; Dahl, A.R.; Bechtold, W.E. [and others

    1995-12-01

    1,3-Butadiene (BD), a gaseous compound used in the production of rubber, is a potent carcinogen in mice and a weak carcinogen in rats. The mechanism of BD-induced carcinogenicity is thought to involve genotoxic effects of its reactive epoxide metabolites butadiene monoepoxide (BDO) and butadiene diepoxide (BDO{sub 2}). Studies in our laboratory have shown that levels of the epoxides, particularly BDO{sub 2}, are greater in mice-the more sensitive species-than rats. While both epoxides are genotoxic in a number of assays, BDO{sub 2} is mutagenic in TK6 human lymphoblastoid cells at concentrations approximately 100-fold lower than BDO. Species differences in carcinogenicity of BD have posed a dilemma to investigators deciding which animal model is most appropriate for BD risk assessment.

  13. Study of the Influence of adding styrene-ethylene/butadiene-styrene in acrylonitrile-butadiene-styrene and polyethylene blends

    OpenAIRE

    M.A. Peydro; F. Parres; Navarro Vidal, Raúl; Sanchez-Caballero, Samuel

    2014-01-01

    This work studies the recovery of two grades of acrylonitrile butadiene styrene (ABS) contaminated with low-density polyethylene (LDPE), by adding styrene ethylene/butadiene styrene (SEBS). To simulate contaminated ABS, virgin ABS was mixed with 1, 2, 4, and 8% of LDPE and then extruded at 220°C. After this, the ABS with the highest percentage of LDPE (8%) was mixed with 1, 2, 4, and 8% of SEBS and then extruded. Different blends were mechanically, rheologically, optically, and dimensionally ...

  14. Chemocatalytic conversion of ethanol into butadiene and other bulk chemicals.

    Science.gov (United States)

    Angelici, Carlo; Weckhuysen, Bert M; Bruijnincx, Pieter C A

    2013-09-01

    The development of new and improved processes for the synthesis of bio-based chemicals is one of the scientific challenges of our time. These new discoveries are not only important from an environmental point of view, but also represent an important economic opportunity, provided that the developed processes are selective and efficient. Bioethanol is currently produced from renewable resources in large amounts and, in addition to its use as biofuel, holds considerable promise as a building block for the chemical industry. Indeed, further improvements in production, both in terms of efficiency and feedstock selection, will guarantee availability at competitive prices. The conversion of bioethanol into commodity chemicals, in particular direct 'drop-in' replacements is, therefore, becoming increasingly attractive, provided that the appropriate (catalytic) technology is in place. The production of green and renewable 1,3-butadiene is a clear example of this approach. The Lebedev process for the one-step catalytic conversion of ethanol to butadiene has been known since the 1930s and has been applied on an industrial scale to produce synthetic rubber. Later, the availability of low-cost oil made it more convenient to obtain butadiene from petrochemical sources. The desire to produce bulk chemicals in a sustainable way and the availability of low-cost bioethanol in large volumes has, however, resulted in a renaissance of this old butadiene production process. This paper reviews the catalytic aspects associated with the synthesis of butadiene via the Lebedev process, as well as the production of other, mechanistically related bulk chemicals that can be obtained from (bio)ethanol. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  15. Modifikation und Molmassenreduktion von Acrylnitril-Butadien-Copolymeren mittels Olefinmetathese

    OpenAIRE

    Schneider, Martin Ferdinand

    2010-01-01

    Hydrierter Nitrilkautschuk (H-NBR) zeichnet sich durch hervorragende mechanische Eigenschaften und sehr gute Beständigkeit gegen hohe Temperaturen sowie Öle aus. Bei der Herstellung einiger H-NBR-Typen wird die Molmasse der Vorstufen, der Acrylnitril-Butadien-Copolymere, durch Olefinmetathese reduziert. Die Untersuchung dieses Metatheseschritts, sowie die Modifikation des Kautschuks mit Hilfe dieser Reaktion war Ziel dieser Arbeit. Es wurden neuartige Katalysatoren getestet, sowie die Eigensc...

  16. Thermal Stability and Flammability of Styrene-Butadiene Rubber-Based (SBR) Ceramifiable Composites

    National Research Council Canada - National Science Library

    Anyszka, Rafał; Bieliński, Dariusz; Pędzich, Zbigniew; Rybiński, Przemysław; Imiela, Mateusz; Siciński, Mariusz; Zarzecka-Napierała, Magdalena; Gozdek, Tomasz; Rutkowski, Paweł

    2016-01-01

    Ceramifiable styrene-butadiene (SBR)-based composites containing low-softening-point-temperature glassy frit promoting ceramification, precipitated silica, one of four thermally stable refractory fillers...

  17. Synthesis and properties of butadiene-alpha-methylstyrene thermoplastic elastomer

    Directory of Open Access Journals (Sweden)

    A. V. Firsova

    2016-01-01

    Full Text Available Butadiene-α-methylstyrene block – copolymer – a thermoplastic elastomer (TPE-R DMST occupies a special place among the ethylene – vinyl aromatic block copolymers. TPE-R DMST comprising as plastic – poly-α-methylstyrene unit and elastic – polybutadiene block. TPE-R DMST has high heat resistance, flexibility, abrasion resistance compared to butadiene-styrene thermoplastic elastomer (TPE DST. The synthesis of block copolymers of butadiene and α-methylstyrene was carried out. The process of polymerization the α-methylstyrene characterized the high speed of polymerization in polar medium and low reaction speed in hydrocarbon solvents. Anionic catalyst nbutyllithium (n-BuLi and high concentration – 60–80% α-methylstyrene in the mixture influenced by synthesis of the 1st block of TPE-R DMST, it’s technologically difficult. Found that the low temperature of polymerization α-methylstyrene (+61 o C, the reversibility of these reactions and the high concentration of residual monomer are very importance. It was revealed that a high polymerization rate α-methylstyrene can be achieved by conducting the reaction in a hydrocarbon solvent with polar additives compounds such as tetrahydrofuran (THF and methyl tert-butyl ether (MTBE. The conditions for the synthesis of P-DMST were developed. The kinetics of polymerization for the first DMST-P unit was obtained. Analysis of physical and mechanical properties DMST-P samples was conducted. The optimum content of bound α-methylstyrene block copolymer provides a good combination of properties in a relatively wide temperature range. The tensile strength at normal and elevated temperatures, the hardness and the stiffness of the polymer increased by increasing the content of bound α-methylstyrene. The elongation and the elasticity reduced by increasing the content of bound α-methylstyrene.

  18. 40 CFR 63.500 - Back-end process provisions-carbon disulfide limitations for styrene butadiene rubber by emulsion...

    Science.gov (United States)

    2010-07-01

    ... disulfide limitations for styrene butadiene rubber by emulsion processes. 63.500 Section 63.500 Protection... limitations for styrene butadiene rubber by emulsion processes. (a) Owners or operators of sources subject to this subpart producing styrene butadiene rubber using an emulsion process shall operate the process...

  19. Excited State Spectra and Dynamics of Phenyl-Substituted Butadienes

    DEFF Research Database (Denmark)

    Wallace-Williams, Stacie E.; Schwartz, Benjamin J.; Møller, Søren

    1994-01-01

    A combination of steady-state and dynamic spectral measurements are used to provide new insights into the nature of the excited-state processes of all-trans-1,4-diphenyl-1,3-butadiene and several analogs: 1,4-diphenyl- 1,3-cyclopentadiene, 1,1,4,4-tetraphenylbutadiene, 1,2,3,4-tetraphenyl-1,3-cyc...... indicate that phenyl torsional motion is not important to the excited-state dynamics and reveal alternative excited-state reaction pathways. The results demonstrate how molecular systems that are structually similar can exhibit different electronic properties and excited-state dynamics....

  20. Devulcanization of styrene butadiene (SBR) waste tire by controlled oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Rios, Rachel R.V.A.; Gontijo, Manuela; Ferraz, Vany P.; Lago, Rochel M.; Araujo, Maria Helena [Minas Gerais Univ., Belo Horizonte, MG (Brazil). Dept. de Quimica]. E-mail: mharaujo@ufmg.br

    2006-05-15

    This work describes the devulcanization of vulcanized SBR (Styrene Butadiene Rubber) based on controlled oxidation with nitric acid. IR, {sup 1}H and {sup 13}C-NMR, CHN elemental analyses, TG, GPC and TPD-MS (Temperature Programmed Decomposition-Mass Spectrometry) experiments suggest that nitric acid promotes two processes: devulcanization by oxidation of the sulfide crosslinks and oxidation of the carbon framework leading to the formation of -COOH and -NO{sub 2} groups. Under aggressive conditions (HNO{sub 3}, reflux) the polymer chain is strongly oxidized and fragmented to a highly oxygenated low molecular weight fraction, which is soluble in water. (author)

  1. [The airborne 1,3-butadiene concentrations in rubber and plastic processing plants].

    Science.gov (United States)

    Yoshida, Toshiaki; Tainaka, Hidetsugu; Matsunaga, Ichiro; Goto, Sumio

    2002-03-01

    Environment pollution by 1,3-butadiene had considerably increased in Japan. The main cause of the pollution is the automotive exhaust gas, and leaks from factories, smoking, and burning of rubber and plastic products are considered to be minor sources. The object of this study was to determine the contamination levels of airborne 1,3-butadiene in factories processing rubber and plastics containing 1,3-butadiene. The concentrations of airborne 1,3-butadiene were measured in 21 plants (10 rubber processing plants and 11 plastics processing plants) in Osaka. 1,3-Butadiene in air was collected for 10 minutes with a charcoal tube and a portable small pump adjusted to a 250 ml/min flow rate. In each plant, indoor air samples at five points and an outdoor air sample at one point outside the plant were collected. The samples were subjected to gas chromatography/mass spectrometry after thermal desorption from the charcoal. The concentrations of airborne 1,3-butadiene in the rubber processing plants and the plastics processing plants were 0.14-2.20 micrograms/m3 (geometric mean: 0.48 microgram/m3) and 0.23-4.51 micrograms/m3 (geometric mean: 0.80 microgram/m3), respectively. In all plants examined, indoor 1,3-butadiene concentrations were higher than the outdoor concentrations around the plants. Therefore, 1,3-butadiene was considered to arise from the processing of rubber or plastics, but the indoor 1,3-butadiene concentrations were much lower than the PEL-TWA (1 ppm = 2.21 mg/m3) of OSHA and the TLV-TWA (2 ppm) of ACGIH. The concentrations in the plants with closed room conditions without ventilation were higher than the concentrations in the other plants. It was suggested that ventilation affected the 1,3-butadiene concentration in the plants.

  2. SYNTHESIS OF STYRENE-BUTADIENE STATISTIC COPOLYMERS CONTAINING MAGNESIUM INITIATOR

    Directory of Open Access Journals (Sweden)

    A. V. Firsova

    2015-01-01

    Full Text Available The article discusses the use of organomagnesium initiators in the synthesis of styrene-butadiene random copolymer (SBR obtained solution polymerization and their influence on the properties of rubber. Selected organic magnesium dialkyl initiator is combined with a modifier, which is a mixed alkoxide of an alkali and alkaline earth metals, which allows to control the micr ostructure of the diene polymer and its molecular weight characteristics. Alcohol derivatives selected high-boiling alcohols tetra (hydroxypropyl ethylenediamine (lapromol 294 and tetrahydrofurfuryl alcohol (TGFS. Selection of high-boiling alcohols due to the fact that the destruction of alkoxide with aqueous polymer degassing they do not fall into the return solvent and almost fall into the exact water. The metal components of alkoxides are lithium, sodium, potassium, magnesium and calcium. The resulting solutions are stable when stored modifier t hroughout the year even at -40 °C. The scheme of obtaining the new catalyst systems based organomagnesium and alcoxide of alkali and alkaline earth metals, which yields as functionalized SBR with a statistical and a distribution block of butadiene and styrene was developed. The process of copolymerization with styrene to butadiene organomagnesium initiators as using an organolithium compound (n-butyllithium was carried out, and without it. Found that the addition of n-butyllithium in the reaction mixture leads to a sharp increase in the rate of reaction. The results of studies of the effect of composition of the initiator system on the structure of diene polymers. It was revealed that a mixed initiator system affords a high conversion of monomers (to 90 % in 1 hour 1,2-polybutadiene content increased to 60 %. The process of polymerization of only a mixture of organomagnesium initiators and alcoxide of alkali and alkaline earth metals are not actively proceeds, conversion of the monomers reaches to 90 % in 4 hours, the microstructure

  3. Preparation of acrylonitrile butadiene styrene fibers by pulse electrospinning

    Directory of Open Access Journals (Sweden)

    Dilyara Igimbayeva

    2014-12-01

    Full Text Available The paper represents the results on the preparation of polymer fibers of acrylonitrile butadiene styrene (ABS with the addition of iron as a modifying additives by pulse electrospinning. The virtue of the method of pulse electrospinning in comparison with classical electrospinning is to obtain fibers with a controlled length. To study the morphology of the fibers obtained samples were used the optical and scanning electron microscopy. To prove the presence of iron inside the fibers methods of elemental analysis and electron paramagnetic resonance were used. The technique and optimal conditions for obtaining fibers have been determined. The effect of technological parameters, concentrations of polymer solutions and modifying additives on the structure and morphology of the fibers were shown.

  4. Reactive processing of recycled polycarbonate/acrylonitrile butadiene styrene.

    Science.gov (United States)

    Jung, Woo-Hyuk; Choi, Yeon-Sil; Moon, Jung-Min; Tortorrela, Nathan; Beatty, Charles L; Lee, Jang-Oo

    2009-04-01

    Cellular phone housings were ground to make original particulates using a knife mill. Foams and adhesives with a lighter density than water were removed from ground mixtures using a sink-float process in water; ground metals, button rubbers, and wires were separated from desired materials by using a sink float process in salt All housing materials, consisting of seven thermoplastics included in cellular phone housings, showed better tensile properties than pure housing materials made of polycarbonate/acrylonitrile butadiene styrene, but they only had about half of the impact strength. In contrast, the low impact strength for all housing materials was improved by adding 25 wt % polyethylene elastomer and/or 2.4 wt % ground epoxy circuit boards for batch mixing. Impact strengths, tensile strengths, and the energy absorption ability of all housing materials were improved by adding 5.4wt% glycidyl methacrylate for twin screw extrusion.

  5. Synthesis of novel N-, S-substituted-polyhalo-1, 3-butadienes and ...

    Indian Academy of Sciences (India)

    polyhalodiene-2-nitro-1, 3-butadiene derivatives. Most of these reactions were found to be highly selective resulting in good to high yields of the products. All new compounds have been characterized by nuclear magnetic resonance spectroscopy (NMR), ...

  6. Crack initiation and propagation on the polymeric material ABS (Acrylonitrile Butadiene Styrene), under ultrasonic fatigue testing

    National Research Council Canada - National Science Library

    G M Domínguez Almaraz; E Correa Gómez; JC Verduzco Juárez; JL Avila Ambriz

    2015-01-01

    ... (Acrylonitrile Butadiene Styrene), under ultrasonic fatigue testing. Three controlled actions were implemented in order to carry out fatigue tests at very high frequency on this material of low thermal conductivity, they are: a...

  7. Impact behaviour of acrylonitrile-butadiene-styrene after temperature and humidity load

    OpenAIRE

    Hylova Lenka; Manas Miroslav

    2017-01-01

    This study deals with acrylonitrile-butadiene-styrene (ABS) which was subjected the drop-weight test before and after temperature and humidity load. ABS is an engineering plastic and also an important engineering terpolymer, which has butadiene part uniformly distributed through the acrylonitrile-styrene matrix and is commonly used in production of automotive interior components. The injection moulded ABS samples were subjected the penetration test at fall height 100 J before and after temper...

  8. Morphology and Phase Transitions in Styrene-Butadiene-Styrene Triblock Copolymer Grafted with Isobutyl Substituted Polyhedral Oligomeric Silsesquioxanes (Postprint)

    National Research Council Canada - National Science Library

    Drazowski, Daniel B; Lee, Andre; Haddad, Timothy S

    2007-01-01

    Two symmetric triblock polystyrene-butadiene-polystyrene (SBS) copolymers with different styrene content were grafted with varying amounts of isobutyl-substituted polyhedral oligomeric silsesquioxane (POSS) molecules...

  9. Fatigue Characteristics of 3D Printed Acrylonitrile Butadiene Styrene (ABS)

    Science.gov (United States)

    Padzi, M. M.; Bazin, M. M.; Muhamad, W. M. W.

    2017-11-01

    Recently, the use of 3D printer technology has become significant to industries, especially when involving the new product development. 3D printing is a technology, which produces the 3D product or prototype using a layer-by-layer technique. However, there becomes less research on the mechanical performance of the 3D printed component. In the present work, fatigue characteristics of 3D printed specimen have been studied. Acrylonitrile butadiene styrene (ABS) has been chosen as a material research due to its wide applications. Two types of specimen used, which is the 3D printing and moulding specimens. Fused deposition modelling (FDM) technique was used to produce the specimens. The dog bone shape part was produced based on ASTM D638 standard and the tensile test has been carried out to get the mechanical properties. Fatigue test was carried out at 40%, 60% and 80% of the tensile strength. The moulded part shows higher fatigue cycles compared to 3D printed part for all loading percentages. Fatigue lives for 40%, 60% and 80%, were 911, 2645 and 26948 cycles, respectively. The results indicated that 3D printed part has a lower fatigue life, which may not suitable for industrial applications. However, the 3D printed part could be improved by using various parameters and may be introduced in low strength application.

  10. Molecular Simulation of Gas Solubility in Nitrile Butadiene Rubber.

    Science.gov (United States)

    Khawaja, M; Sutton, A P; Mostofi, A A

    2017-01-12

    Molecular simulation is used to compute the solubility of small gases in nitrile butadiene rubber (NBR) with a Widom particle-insertion technique biased by local free volume. The convergence of the method is examined as a function of the number of snapshots upon which the insertions are performed and the number of insertions per snapshot and is compared to the convergence of the unbiased Widom insertion technique. The effect of varying the definition of local free volume is also investigated. The acrylonitrile content of the polymer is altered to examine its influence on the solubility of helium, CO2, and H2O, and the solubilities of polar gases are found to be enhanced relative to those of nonpolar gases, in qualitative agreement with experiment. To probe this phenomenon further, the solubilities are decomposed into contributions from the neighborhoods of different atoms, using a Voronoi cell construction, and a strong bias is found for CO2 and H2O in particular to be situated near nitrogen sites in the elastomer. Temperature is shown to suppress the solubility of CO2 and H2O but to increase that of helium. Increasing pressure is found to suppress the solubility of all gases but at different rates, according to a balance between their molecular sizes and electrostatic interactions with the polymer. These results are relevant to the use of NBR seals at elevated temperatures and pressures, such as in oil and gas wells.

  11. Bioaccumulation factors for chlorinated benzenes, chlorinated butadienes and hexachloroethane

    Energy Technology Data Exchange (ETDEWEB)

    Burkhard, L.P. [Environmental Protection Agency, Duluth, MN (United States). National Health and Environmental Effects Research Lab.; Sheedy, B.R. [AScI Corp., Duluth, MN (United States); McCauley, D.J.; DeGraeve, G.M. [Battelle-Great Lakes Environmental Center, Traverse City, MI (United States)

    1997-08-01

    A field study was performed that measured bioaccumulation factors (BAFs) for chlorinated benzenes, chlorinated butadienes, and hexachloroethane in four species, Fundulus heteroclitus (mummichog), Callinectes sapidus (blue crabs), Brevoortia patronus (gulf menhaden), and Micropoganias undulatus (Atlantic croaker). The measured BAFs were not significantly different among the fishes. The measured BAFs for the C. sapidus were in good agreement with those measured for the fishes except for hexachloroethane (HCE), E- and Z-1,1,2,3,4-pentachlorobuta-1,3-diene (E-and Z-PeCBD), and hexachlorobuta-1,3-diene (HCBD). Their measured BAFs were approximately an order of magnitude smaller than those measured for the fishes. The measured BAFs were also in good agreement with BAFs reported/derived from the literature and to BAFs predicted using two methods of the Environmental Protection Agency (EPA) except for HCE, E- and Z-PeCBD, and HCBD in the C. sapidus. These BAFs were much smaller than the reported/derived and predicted BAFs. The smaller BAFs for HCE, E- and Z-PeCBD, and HCBD were consistent with the metabolism abilities for the C. sapidus, and metabolism processes are believed to be the cause for the smaller BAFs. The predicted BAFs were within a factor of five of the measured BAFs for 90% (n = 48) and 94% (n = 32) using the two methods of the EPA.

  12. 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.

  13. Application of Lignin as Antioxidant in Styrene Butadiene Rubber Composite

    Science.gov (United States)

    Liu, Shusheng; Cheng, Xiansu

    2010-11-01

    Lignin isolated from enzymatic hydrolyzed cornstalks (EHL) is a renewable natural polymer, and rubber is one of the most important polymer materials. The application of EHL in rubber industry is of great significance. The influence of EHL and antioxidant RD on the vulcanizing characteristics, thermal oxidative aging stability under free condition, and water extraction resistance of styrene-butadiene rubber (SBR) were investigated. The effect of EHL/antioxidant D composite antioxidant on the thermal oxidative ageing of SBR was also evaluated. Results showed that the protection of SBR from thermal oxidative aging by EHL/antioxidant D composite antioxidant was superior to that of antioxidant D. This is because EHL molecules have hindered phenol group and have excellent auxiliary antioxidant role with antioxidant D. Moreover, the influence of EHL on the vulcanizing characteristics of SBR compounds was better than that of antioxidant RD, and EHL can reduce the cure rate and increase the optimum cure time. It is because that the EHL molecules have hindered phenol group and methoxy group, which can form a special structure to capture free radical and terminate the chain reaction. The retained tensile strength of SBR compounds with EHL was similar to that of the samples with antioxidant RD, while the retained elongation at break of SBR compounds with EHL was higher than that of the samples with antioxidant RD. In addition, the SBR compounds with EHL have a good water extraction resistance property, which was similar to the samples with antioxidant RD. This is because EHL have large molecular weight, good stability and low solubility in water. In conclusion, due to the low price, abundant resources, non-toxic and pollution-free, etc., EHL will have broad application prospect.

  14. Inhalation toxicity studies with 1,3-butadiene. 2. 3 month toxicity study in rats

    Energy Technology Data Exchange (ETDEWEB)

    Crouch, C.N.; Pullinger, D.H.; Gaunt, I.F.

    1979-09-01

    The available toxicological data for 1,3-butadiene are limited and contradictory. Three month toxicity and two year carcinogenicity studies have therefore been initiated to identify any potential hazard to occupationally exposed personnel. The results of the 3 month study are reported in this paper. Five groups of Sprague-Dawley rats were exposed to 1,3-butadiene gas at atmospheric concentrations of 0, 1000, 2000, 4000, and 8000 ppM v/v respectively, 6 hours/day, 5 days/week for 13 weeks. No untoward effects attributable to exposure were observed, except a moderately increased salivation, particularly in female animals during the last 5 to 8 weeks of exposure, at higher concentrations of butadiene.

  15. Chrome-tanned leather shavings as a filler of butadiene-acrylonitrile rubber.

    Science.gov (United States)

    Przepiórkowska, A; Chrońska, K; Zaborski, M

    2007-03-06

    The noxious wastes from the tanning industry such as chrome-tanned leather shavings were used as the only filler of rubber mixes containing carboxylated butadiene-acrylonitrile rubber (XNBR) or butadiene-acrylonitrile rubber (NBR), and a dispersing agent Limanol PEV (Schill & Seilacher). The best form addition of leather powder to the rubber mixes is mixed the waste protein with zinc oxide. The leather powder added to the rubber mixes improves the mechanical properties: tensile strength (T(s)), elongation at break (epsilon(b)) and increase the cross-linking density of carboxylated XNBR and NBR rubber mixes. Satisfactory results of these studies are presented in this work.

  16. Impact behaviour of acrylonitrile-butadiene-styrene after temperature and humidity load

    Directory of Open Access Journals (Sweden)

    Hylova Lenka

    2017-01-01

    Full Text Available This study deals with acrylonitrile-butadiene-styrene (ABS which was subjected the drop-weight test before and after temperature and humidity load. ABS is an engineering plastic and also an important engineering terpolymer, which has butadiene part uniformly distributed through the acrylonitrile-styrene matrix and is commonly used in production of automotive interior components. The injection moulded ABS samples were subjected the penetration test at fall height 100 J before and after temperature and humidity load and the results were subsequently evaluated and discussed. It was found out that ABS after temperature and humidity load has lower impact resistance.

  17. Modeling butadiene adsorption on oxidized graphene surface using density functional theory

    Science.gov (United States)

    Akimenko, Ju. Y.; Akimenko, S. S.; Gorbunov, V. A.

    2017-08-01

    In this paper, the process of chemisorption of cis-butadiene rubber on the surface of oxidized graphene was studied using the density functional theory. The polymer is interacting to a quinone group, an oxygen bridge, and an OH group which was differently located on the surface of the graphene sheet. Based on the calculated value of ΔG298, the possibility of spontaneous formation of the bond between butadiene rubber and these functional groups was estimated. The features of the temperature dependence of the change in free Gibbs energy for thermodynamically possible coupled systems are considered.

  18. Transition-Metal-Free Synthesis of 1,3-Butadiene-Containing π-Conjugated Polymers.

    Science.gov (United States)

    Cai, Xuediao; Liu, Yating; Lu, Tian; Yang, Rui; Luo, Chuxin; Zhang, Qi; Chai, Yonghai

    2016-12-01

    This work describes the synthesis of π-conjugated polymers possessing arylene and 1,3-butadiene alternating units in the main chain by the reaction of α,β-unsaturated ester/nitrile containing γ-H with aromatic/heteroaromatic aldehyde compound. By using 4-(4-formylphenyl)-2-butylene acid ethyl ester as a model monomer, the different polymerization conditions, including catalyst, catalyst amount, and solvent, are optimized. The polymerization of 4-(4-formylphenyl)-2-butylene acid ethyl ester is carried out by refluxing in ethanol for 72 h with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) as a catalyst to give a 1,3-butadiene-containing π-conjugated polymer, poly(phenylene-1,3-butadiene), in 84.3% yield with M¯n and M¯w/M¯n (PDI) estimated as 6172 and 1.65, respectively. Based on this new methodology, a series of π-conjugated polymers containing 1,3-butadiene units with different substituents are obtained in high yields. A possible mechanism is proposed for the polymerization through a six-membered ring transition state and then a 1,5-H shift intermediate. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  19. Highly active catalysts for the telomerization of crude glycerol with 1,3-butadiene

    NARCIS (Netherlands)

    Palkovits, R.; Nieddu, I.; Klein Gebbink, R.J.M.; Weckhuysen, B.M.

    2008-01-01

    The first description of a telomerization reaction came from Smutny in 1967 who was studying the oligomerization and dimerization of 1,3-butadiene and its reactions with nucleophiles. Since then, numerous studies have appeared concentrated on monofunctional alcohols and other simple nucleophiles

  20. Particle reinforced composites from acrylamide modified blend of styrene-butadiene and natural rubber

    Science.gov (United States)

    Blends of styrene-butadiene rubber and natural rubber that provide balanced properties were modified with acrylamide and reinforced with soy protein particles. The rubber composites show improved mechanical properties. Both modified rubber and composites showed a faster curing rate. The crosslinking...

  1. Polymer composites prepared from heat-treated starch and styrene-butadiene latex

    Science.gov (United States)

    Thermoplastic starch/latex polymer composites were prepared using styrene–butadiene (SB) latex and heat-treated cornstarch. The composites were prepared in a compression mold at 130 °C, with starch content 20%. An amylose-free cornstarch, waxy maize, was used for this research and the heat treatment...

  2. Short-term toxicity and reproduction studies in rats with hexachloro-(1,3)-butadiene

    NARCIS (Netherlands)

    Harleman, J.H.; Seinen, W.

    In rats given daily doses of 0. 0.4, 1.0, 2.5, 6.3, and 15.6 mg of hexachloro-(1,3)-buta-diene (HCBD)/kg by gavage for 13 weeks, no effect levels of 1.0 and 2.5 mg/kg were established for females and males, respectively. Inhibition of growth occurred in both sexes at the two highest doses and

  3. 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.

  4. Performance Analysis of Styrene Butadiene Rubber-Latex on Cement Concrete Mixes.

    OpenAIRE

    Er. Kapil Soni; Dr. Y.P Joshi

    2014-01-01

    To improve the performance of concrete, polymers are mixed with concrete. It has been observed that polymer-modified concrete (PMC) is more durable than conventional concrete due to superior strength and high durability. In this research, effect of Styrene-Butadiene Rubber (SBR) latex on compressive strength and flexural strength of concrete has been studied and also the optimum polymer (SBR-Latex) content for concrete is calculated. This research was carried out to establish t...

  5. Microstructural analysis of carbon nanomaterials produced from pyrolysis/combustion of Styrene-Butadiene-Rubber (SBR)

    OpenAIRE

    Alves, Joner Oliveira; Zhuo, Chuanwei; Levendis, Yiannis Angelo; Tenório, Jorge Alberto Soares

    2011-01-01

    Styrene-Butadiene-Rubber (SBR) is a synthetic rubber copolymer used to fabricate several products. This study aims to demonstrate the use of SBR as feedstock for carbon nanomaterials (nanofibers and nanotubes) growth, and therefore to establish a novel process for destination of waste products containing SBR. A three stage electrically heated flow reactor was used. Small pellets of rubber were pyrolyzed at a temperature of 1000 ºC. The pyrolyzates were mixed with oxygen-containing gases and w...

  6. Mechanical and Electrical Properties of Acrylonitrile Butadiene Styrene/Melamine-Functionalized Reduced Graphene Oxide Nanocomposites.

    Science.gov (United States)

    Oh, Miae; Rajagopalan, Balasubramaniyan; Chung, Jin Suk

    2015-11-01

    Nanocomposite of acrylonitrile butadiene styrene (ABS) and melamine functionalized reduced graphene oxide (M-RGO) was prepared by solution blending. The functionalization of graphene oxide was performed with melamine to increase the compatibility between graphene sheets and the ABS matrix. The ABS/M-RGO showed improved storage modulus by 55% at 4.0 wt% of M-RGO in the glassy region and exhibited a low percolation threshold with a high electrical conductivity.

  7. An isotopic dilution approach for 1,3-butadiene tailpipe emissions and ambient air monitoring.

    Science.gov (United States)

    Riservato, Manuela; Rolla, Antonio; Davoli, Enrico

    2004-01-01

    An isotopic dilution approach for 1,3-butadiene analysis in gaseous samples is presented. The methodology is based on active sampling on sorbent tubes and subsequent analysis by thermal desorption into a gas chromatography/mass spectrometry system. By adding a perdeuterated internal standard onto the sorbent tubes before sampling, and using mass spectrometric detection, the methodology gives high accuracy for this unstable analyte. The method has been used to monitor 1,3-butadiene ambient air concentrations in a residential area in proximity to a heavy-traffic roadway over a one-week period, for comparison with other traffic-related pollutants analysed by standard procedures. It has also been used to determine tailpipe emissions of two vehicles by standard emission testing procedures in a dynamometer. These vehicles were chosen as examples of low- and high-end emission rate vehicles, i.e., an old no-catalytic converter Otto engine and a new direct-injection diesel engine with catalytic converter. Exhaust gas emissions were 0.052 and 35.85 mg/km, reflecting differences in fuel, engine design, age, and presence (or not) of a catalytic abatement system. The ambient air results showed a weekly average concentration of 1,3-butadiene of 0.53 microg/m(3). Copyright 2004 John Wiley & Sons, Ltd.

  8. Inhalation developmental toxicology studies: Teratology study of 1,3-butadiene in mice: Final report

    Energy Technology Data Exchange (ETDEWEB)

    Hackett, P.L.; Sikov, M.R.; Mast, T.J.; Brown, M.G.; Buschbom, R.L.; Clark, M.L.; Decker, J.R.; Evanoff, J.J.; Rommereim, R.L.; Rowe, S.E.; Westerberg, R.B.

    1987-11-01

    Maternal toxicity, reproductive performance and developmental toxicology were evaluated in CD-1 mice following whole-body, inhalation exposures to 0, 40, 200 and 1000 ppM of 1,3-butadiene. The female mice, which had mated with unexposed males were exposed to the chemical for 6 hours/day on 6 through 15 dg and sacrificed on 18 dg. Maternal animals were weighed prior to mating and on 0, 6, 11 and 18 dg; the mice were observed for mortality, morbidity and signs of toxicity during exposure and examined for gross tissue abnormalities at necropsy. Live fetuses were weighed and subjected to external, visceral and skeletal examinations to detect growth retardation and morphologic anomalies. Significant concentration-related decreases were detected in a number of maternal body weight measures. There was a significant concentration-related depression of fetal body weights and placental weights. Body weights of male fetuses of all exposed groups were significantly lower than values for control fetuses; weights of female fetuses were significantly depressed in the mice exposed to 200 and 1000 ppM. In the 200- and 1000-ppM exposure groups, weights of placentas of male fetuses were significantly decreased, but placental weights of female fetuses were significantly affected only in litters exposed to the highest 1,3-butadiene concentration. This exposure regimen produced significant signs of maternal toxicity at concentrations of 200 and 1000 ppM 1,3-butadiene.

  9. Polybutadiene and Styrene-Butadiene rubbers for high-dose dosimetry

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Lucas N. [Instituto Federal de Educacao, Ciencia e Tecnologia de Goias-IFG,Campus Goiania, Goiania -GO (Brazil); Instituto de Pesquisas Energeticas e Nucleares -IPEN, Sao Paulo-SP (Brazil); Vieira, Silvio L. [Instituto de Fisica, Universidade Federal de Goias-UFG, Campus Samambaia, Goiania-GO (Brazil); Schimidt, Fernando [Instituto Federal de Educacao, Ciencia e Tecnologia de Goias-IFG,Campus Inhumas, Inhumas-GO (Brazil); Antonio, Patricia L.; Caldas, Linda V.E. [Instituto de Pesquisas Energeticas e Nucleares -IPEN, Sao Paulo-SP (Brazil)

    2015-07-01

    Polybutadiene and Styrene-Butadiene are synthetical rubbers used widely for pneumatic tires manufacturing. In this research, the dosimeter characteristics of those rubbers were studied for application in high-dose dosimetry. The rubber samples were irradiated with doses of 10 Gy up to 10 kGy, using a {sup 60}Co Gamma Cell-220 system (dose rate of 1.089 kGy/h) and their readings were taken on a Fourier Transform Infrared Spectroscopy-FTIR system (model Frontier/Perkin Elmer). The ratios of two absorbance peaks were taken for each kind of rubber spectrum, Polybutadiene (1306/1130 cm{sup -1}) and Styrene-Butadiene (1449/1306 cm{sup -1}). The ratio calculated was used as the response to the irradiation, and is not uniform across the sample. From the results, it can be concluded for both rubbers: a) the dose-response curves may be useful for high-dose dosimetry (greater than 250 Gy); b) their response for reproducibility presented standard deviations lower than 2.5%; c) the relative sensitivity was higher for Styrene-Butadiene (1.86 kGy{sup -1}) than for Polybutadiene (1.81 kGy{sup -1}), d) for doses of 10 kGy to 200 kGy, there was no variation in the dosimetric response. Both types of rubber samples showed usefulness as high-dose dosimeters. (authors)

  10. Enhancing mechanical and thermal properties of styrene-butadiene rubber/carboxylated acrylonitrile butadiene rubber blend by the usage of graphene oxide with diverse oxidation degrees

    Science.gov (United States)

    Xue, Xiaodong; Yin, Qing; Jia, Hongbing; Zhang, Xuming; Wen, Yanwei; Ji, Qingmin; Xu, Zhaodong

    2017-11-01

    Graphene oxide (GO) with various oxidation degrees were prepared through a modified Hummer's method by varying the dosage of oxidizing agent. Styrene-butadiene rubber (SBR)/carboxylated acrylonitrile butadiene rubber (XNBR)/GO nanocomposites were fabricated by aqueous-phase mixing of GO colloidal dispersion with SBR latex and a small loading of XNBR latex, followed by co-coagulation. Effects of GO oxidation degree on the morphology, structure, mechanical and thermal properties of nanocomposites were thoroughly investigated. The results showed that the mechanical strength of nanocomposites were enhanced with the increase of oxidation degree of GO. Especially, when the weight ratio of KMnO4 to graphite was 15/5, the tensile strength, tear strength and thermal conductivity of SBR/XNBR/GO filled with 3 phr (parts per hundred rubber) GO increased by 255.3%, 141.5% and 22.8%, respectively, compared to those of neat SBR/XNBR blend. In addition, the thermal stability and the solvent resistance of the nanocomposites were also improved significantly. This work suggested that GO with higher oxidation degree could effectively improve the properties of SBR/XNBR blend.

  11. Dynamic mechanical analysis of Norsorex/acrylonitrile butadiene rubber blends and their application in vibration control of steel frames

    Directory of Open Access Journals (Sweden)

    Junhong Xu

    2016-08-01

    Full Text Available The damping properties of acrylonitrile butadiene rubber/Norsorex® blends were investigated by dynamic mechanical analysis. The effects of Norsorex on the damping properties of acrylonitrile butadiene rubber/Norsorex blends were also studied. The results showed that 30-phr Norsorex could dramatically improve the damping of 70-phr acrylonitrile butadiene rubber. Compared with acrylonitrile butadiene rubber, the LA value of acrylonitrile butadiene rubber/Norsorex = 70/30 increased to 7.3 × 108 from 3.0 × 108 Pa K and the TA value increased from 26.6 to 28.4 K. To test the new high-damping-performance blends, shaking table tests on a four-story steel frame with viscoelastic damping wall were designed and the simulations were provided for verification. The experimental results indicated that the viscoelastic damping wall controlled the inter-story displacement well under apg = 7 m/s2, which exceeded the specified limit under uncontrolled conditions. The viscoelastic damping wall showed a better control effect on the displacement response than on the acceleration response subjected to El Centro ground motion for the second to fourth stories. The simulation results of SAP2000 structural analysis software showed good agreement with the experimental results. The differences between the acceleration and displacement time-history responses of the steel frame with acrylonitrile butadiene rubber and acrylonitrile butadiene rubber/Norsorex (70/30 were simulated by SAP2000.

  12. Treatment of 1,3-Butadiene in an Air Stream by a Biotrickling Filter and a Biofilter.

    Science.gov (United States)

    Chou, Ming-Shean; Lu, Shu-Ling

    1998-08-01

    This paper presents results obtained from a performance study on the biotreatment of 1,3-butadiene in an air stream using a reactor that consisted of a two-stage, in-series biotrickling filter connected with a three-stage, in-series biofilter. Slags and pig manure-based media were used as packing materials for the biotrickling filter and the biofilter, respectively. Experimental results indicated that, for the biotrickling filter portion, the butadiene elimination capacities were below 5 g/m3/hr for loadings of less than 25 g/m3/hr, and the butadiene removal efficiency was only around 17%. For the biofilter portion, the elimination capacities ranged from 10 to 107 g/m3/hr for loadings of less than 148 g/m3/hr. The average butadiene removal efficiency was 75-84% for superficial gas velocities of 53-142 m/hr and a loading range of 10-120 g/m3/hr. The elimination capacity approached a maximum of 108 g/m3/hr for a loading of 150 g/m3/hr. The elimination rates of butadiene in both the biotrickling filter and biofilter were mass-transfer controlled for influent butadiene concentrations below about 600 ppm for superficial gas velocities of 29-142 m/hr. The elimination capacity was significantly higher in the biofilter than in the biotrickling filter. This discrepancy may be attributed to the higher mass-transfer coefficient and gas-solid interfacial area offered for transferring the gaseous butadiene in the biofilter.

  13. 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. © The Author(s) 2015.

  14. Toxicity of the components of styrene polymers: polystyrene, acrylonitrile-butadiene-styrene (ABS) and styrene-butadiene-rubber (SBR). Reactants and additives.

    Science.gov (United States)

    Fishbein, L

    1984-01-01

    The toxicity of the components of styrene polymers, e.g., polystyrene, ABS and SBR, were reviewed with primary focus on the reactive monomers (except styrene) (e.g., acrylonitrile, butadiene) as well as on impurities and solvents such as benzene, hexane and methylethyl ketone, and additives such as phenyl-2-naphthylamine, di-n-butyl phthalate, and a number of peroxide initiators and flame retardants (e.g., 2,3-dibromopropanol, decadibromodiphenyl oxide and antimony trioxide). It is stressed that toxicity data are generally lacking for the majority of additives employed in the production of styrene polymers. Information is also lacking as to the numbers of individuals at potential risk and the extent of their exposure to the large number of additives employed.

  15. Atmospheric pressure plasma polymerization of 1,3-butadiene for hydrophobic finishing of textile substrates

    Energy Technology Data Exchange (ETDEWEB)

    Samanta, Kartick K; Jassal, Manjeet; Agrawal, Ashwini K, E-mail: ashwini@smita-iitd.co, E-mail: manjeet.jassal@smita-iitd.co [Smart and Innovative Textile Materials Group (SMITA), Department of Textile Technology, Indian Institute of Technology, Hauz Khas, New Delhi-110016 (India)

    2010-02-01

    Atmospheric pressure plasma processing of textile has both ecological and economical advantages over the wet-chemical processing. However, reaction in atmospheric pressure plasma has important challenges to be overcome before it can be successfully used for finishing applications in textile. These challenges are (i) generating stable glow plasma in presence liquid/gaseous monomer, and (ii) keeping the generated radicals active in the presence of contaminants such as oxygen and air. In this study, a stable glow plasma was generated at atmospheric pressure in the mixture of gaseous reactive monomer-1,3-butadiene and He and was made to react with cellulosic textile substrate. After 12 min of plasma treatment, the hydrophilic surface of the cellulosic substrate turned into highly hydrophobic surface. The hydrophobic finish was found to be durable to soap washing. After soap washing, a water drop of 37 {mu}l took around 250 s to get absorbed in the treated sample compared to < 1 s in the untreated samples. The plasma modified samples showed water contact angle of around 134{sup 0}. Both top and bottom sides of the fabric showed similar hydrophobic results in terms of water absorbency and contact angle. The results may be attributed to chemical reaction of butadiene with the cellulosic textile substrate. The surface characterization of the plasma modified samples under SEM and AFM revealed modification of the surface under <100 nm. The results showed that atmospheric pressure plasma can be successfully used for carrying out reaction of 1,3-butadiene with cellulosic textile substrates for producing hydrophobic surface finish.

  16. Inhalation developmental toxicology studies of 1,3-butadiene in the rat: Final report

    Energy Technology Data Exchange (ETDEWEB)

    Hackett, P.L.; Sikov, M.R.; Mast, T.J.; Brown, M.G.; Buschbom, R.L.; Clark, M.L.; Decker, J.R.; Evanoff, J.J.; Rommereim, R.L.; Rowe, S.E.; Westerberg, R.B.

    1987-11-01

    Maternal toxicity, reproductive performance and developmental toxicology were evaluated in Sprague-Dawley-derived rats during and following 6 hours/day, whole-body, inhalation exposures to 0, 40, 200, and 1000 ppM of 1,3-butadiene. The female rats (Ns = 24 to 28), which had mated with unexposed males, were exposed to the chemical from 6 through 15 dg and sacrificed on 20 dg. Maternal animals were weighed prior to mating and on 0, 6, 11, 16 and 20 dg; the rats were observed for mortality, morbidity and signs of toxicity during exposure and examined for gross tissue abnormalities at necropsy. Live fetuses were weighed and subjected to external, visceral and skeletal examinations to detect growth retardation and morphologic anomalies. There were no significant differences among treatment groups in maternal body weights or extragestational weights of rats exposed to 1,3-butadiene concentrations of 40 or 200 ppM, but, in animals exposed to 1000 ppM, significantly depressed body weight gains were observed during the first 5 days of exposure and extragestational weight gains tended to be lower than control values. These results, and the absence of clinical signs of toxicity, were considered to indicate that there was no maternal toxicity at exposure levels of 200 ppM or lower. The percentage of pregnant animals and the number of litters with live fetuses were unaffected by treatment. Under the conditions of this exposure regimen, there was no evidence for a teratogenic response to 1,3-butadiene exposure.

  17. Molecular analysis on the utilization of oil palm empty fruit bunches fiber as reinforcement for acrylonitrile butadiene styrene biocomposites

    Science.gov (United States)

    Hermawan, B.; Nikmatin, S.; Alatas, H.; Sudaryanto; Sukaryo, S. G.

    2017-05-01

    Oil palm empty fruit bunches (OPEFB) was one of the solid waste produced by the palm oil factory and were totally plentiful in biomass. OPEFB fiber used as reinforcement of polymer matrix acrylonitrile butadiene styrene (ABS). The use of FTIR is to see that there is no changes in the molecules of the constituent biocomposite ABS and OPEFB. The reactivity of butadiene and styrene through the double bond- π conjugated system, contributed to the bond reaction with the maleic acid as compatibilizer witch is grafted to the system. It is concluded that the posible grafting reaction occurs by the addition of the MAH to the double bond of the butadiene and styrene. The hydroxyl group of cellulose can interact with this maleic acid to form a bond through the carboxyl group.

  18. Dimensional accuracy of Acrylonitrile Butadiene Styrene injection molded parts produced in a pilot produc

    DEFF Research Database (Denmark)

    Mischkot, Michael; Davoudinejad, Ali; Charalambis, Alessandro

    Injection molding inserts manufactured additively by vat photopolymerization have become a serious option for significantly faster and more economical prototyping and pilot production due to technological progress and advancements in photopolymer materials in the recent years. 10 000 parts...... of a geometry including micro-features have been injection-molded in Acrylonitrile Butadiene Styrene (ABS) with a single 20x20x2.5 mm^3 injection molding insert manufactured in a photopolymer composite material. This research investigates the dimensional accuracy of the injection molded parts as a function...

  19. Metabolic activation and mutagenicity of 4 vinylic monomers (vinyl chloride, styrene, acrylonitrile, butadiene).

    Science.gov (United States)

    Duverger, M; Lambotte, M; Malvoisin, E; de Meester, C; Poncelet, F; Mercier, M

    1981-05-01

    The mutagenic activity and the metabolism of four vinylic monomers; vinyl chloride, styrene, acrylonitrile and butadiene are reviewed. Those chemicals are converted by the mixed function oxidases system of the endoplasmic reticulum into reactive intermediates which can interact with macromolecules within the cell. In order to examine the mutagenic activity of these compounds and their metabolites, different mutagenicity testing systems have been used: tests with S. typhimurium, E. coli, Schizosaccharomyces pombe, Saccharomyces cerevisiae, V79 Chinese Hamster cells, CHO cells, Drosophila melanogaster as well as evaluations of chromosome aberrations.

  20. Influence of the Nanoclay Cloisite 20A Incorporation on Properties of Acrylonitrile Butadiene Styrene (ABS)

    Science.gov (United States)

    Sales, Jorge N.; Silva, Andressa A.; Valenzuela-Diaz, Francisco R.; Moura, Esperidiana A. B.

    This work aims to study the influence of the nanoclay Cloisite 20A incorporation on mechanical properties of ABS (acrylonitrile butadiene styrene). The incorporation of Cloisite 20A was made in two steps; firstly, a masterbatch was preparated and then, it was incorporated in ABS. The Cloisite 20A masterbatch using 40 % of nanoclay and 60 % of SAN (Styrene Acrylonitrile) was prepared in an adiabatic mill. After that, Cloisite 20A masterbarch at 1 and 5 % (wt) was added in ABS. The resulting nanocomposites were characterized by tensile tests and the correlation between properties was discussed.

  1. Precursor effect on the property and catalytic behavior of Fe-TS-1 in butadiene epoxidation

    Science.gov (United States)

    Wu, Mei; Zhao, Huahua; Yang, Jian; Zhao, Jun; Song, Huanling; Chou, Lingjun

    2017-11-01

    The effect of iron precursor on the property and catalytic behavior of iron modified titanium silicalite molecular sieve (Fe-TS-1) catalysts in butadiene selective epoxidation has been studied. Three Fe-TS-1 catalysts were prepared, using iron nitrate, iron chloride and iron sulfate as precursors, which played an important role in adjusting the textural properties and chemical states of TS-1. Of the prepared Fe-TS-1 catalysts, those modified by iron nitrate (FN-TS-1) exhibited a significant enhanced performance in butadiene selective epoxidation compared to those derived from iron sulfate (FS-TS-1) or iron chloride (FC-TS-1) precursors. To obtain a deep understanding of their structure-performance relationship, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Temperature programmed desorption of NH3 (NH3-TPD), Diffuse reflectance UV-Vis spectra (DR UV-Vis), Fourier transformed infrared spectra (FT-IR) and thermal gravimetric analysis (TGA) were conducted to characterize Fe-TS-1 catalysts. Experimental results indicated that textural structures and acid sites of modified catalysts as well as the type of Fe species influenced by the precursors were all responsible for the activity and product distribution.

  2. Aromatic ring formation in opposed-flow diffusive 1,3-butadiene flames

    KAUST Repository

    Moshammer, Kai

    2016-10-17

    This paper is concerned with the formation of one- and two-ring aromatic species in near atmospheric-pressure opposed-flow diffusion flames of 1,3-butadiene (1,3-CH). The chemical structures of two different 1,3-CH/Ar-O/Ar flames were explored using flame-sampling molecular-beam mass spectrometry with both electron and single-photon ionization. We provide mole fraction profiles of 47 components as function of distance from the fuel outlet and compare them to chemically detailed modeling results. To this end, the hierarchically developed model described by Seidel et al. [16] has been updated to accurately comprise the chemistry of 1,3-butadiene. Generally a very good agreement is observed between the experimental and modeling data, allowing for a meaningful reaction path analysis. With regard to the formation of aromatic species up to naphthalene, it was essential to improve the fulvene and the C chemistry description in the mechanism. In particular, benzene is found to be formed mainly via fulvene through the reactions of the CH isomers with CH The n-CH radical reacts with CH forming 1,3-pentadiene (CH), which is subsequently oxidized to form the naphthalene precursor cyclopentadienyl (CH). Oxidation of naphthalene is predicted to be a contributor to the formation of phenylacetylene (CH), indicating that consumption reactions can be of similar importance as molecular growth reactions.

  3. 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.

  4. Stepwise Swelling of a Thin Film of Lamellae-Forming Poly(styrene-b-butadiene) in Cyclohexane Vapor

    DEFF Research Database (Denmark)

    Di, Zhenyu; Posselt, Dorthe; Smilgies, Detlef-M.

    2012-01-01

    We investigated the swelling of a thin film of lamellae-forming poly(styrene-b-butadiene) in cyclohexane vapor. The vapor pressure and thus the degree of swelling of the film are increased in a stepwise manner using a custom-built sample cell. The resulting structural changes during and after eac...

  5. Oxidative Dehydrogenation of n-Butenes to 1,3-Butadiene over Bismuth Molybdate and Ferrite Catalysts: A Review

    KAUST Repository

    Hong, Eunpyo

    2015-11-02

    1,3-Butadiene, an important raw material for a variety of chemical products, can be produced via the oxidative dehydrogenation (ODH) of n-butenes over multicomponent oxide catalysts based on bismuth molybdates and ferrites. In this review, the basic concept, reaction mechanism, and catalysts typically used in an ODH reaction are discussed. © 2015, Springer Science+Business Media New York.

  6. Study of conversion of butadiene to CO2 by rTiO2 nanoparticles: ZINDO/S

    Science.gov (United States)

    Mahdavian, Leila

    2017-02-01

    One of the pollutants emitted from automobile exhaust is unburned hydrocarbons that include benzene, propane, formaldehyde, butadiene, etc. Due to the carcinogenicity of these substances, eliminating and reducing them in the source of production is essential. Catalytic converters have been developed to reduce these pollutions to low-risk materials in automobile exhaust. In this study, the mechanism of converting butadiene to carbon dioxide is simulated and calculated by rutile titanium dioxide (Titania) nanoparticles ( rTiO2-NP). Then the geometric structure of simulated steps (the conversion butadiene to carbon dioxide) is optimized by DFT method and semi-empirical (ZINDO/S) method is used to calculate the thermodynamic properties. There are three different locations of physical chemistry on the rTiO2-NPs to get closer pollutants, namely Ti-O (1), Ti-O (2), and Ti-Ti. The results show the approaching possibility of butadiene to Ti-O (1) is more than other locations, because the bond length, electronegativity and spatial structure of this position are different from others.

  7. Role of Magnesium Silicates in Wet-Kneaded Silica-Magnesia Catalysts for the Lebedev Ethanol-to-Butadiene Process

    NARCIS (Netherlands)

    Chung, Sangho; Angelici, Carlo; Hinterding, Stijn O. M.; Weingarth, Markus; Baldus, Marc; Houben, Klaartje; Weckhuysen, Bert M.; Bruijnincx, Pieter C. A.

    Wet-kneading is a technique commonly used for the synthesis of SiO2–MgO catalysts for the Lebedev ethanol-to-butadiene process, with catalyst performance known to depend heavily on the preparation parameters used in this method. Here, the large influence of Mg precursor and MgO content on

  8. On the form of the strain energy function for a family of SBR materials. [Styrene-Butadiene Rubber

    Science.gov (United States)

    Arenz, R. J.

    1977-01-01

    Styrene-butadiene materials with varying crosslink densities are analyzed through use of a strain energy function of the type introduced by Valanis and Landel (1967). A form of the strain energy function derived from strip biaxial tests proves to be accurate when checked against uniaxial and other biaxial test results.

  9. Ethanol-to-Butadiene Conversion over SiO2-MgO Catalysts: Synthesis-Structure-Performance Relationships

    NARCIS (Netherlands)

    Angelici, C.

    2015-01-01

    The work presented in this PhD Thesis provides new insights into the underlying reasons that make SiO2-MgO materials excellent catalysts for the ethanol-to-butadiene Lebedev process. In particular, the preparation technique of choice affects the structural properties of the resulting SiO2-MgO

  10. Fracture morphologies of carbon-black-loaded SBR (styrene-butadiene rubber) subjected to low-cycle, high-stress fatigue. [Styrene-butadiene rubber

    Energy Technology Data Exchange (ETDEWEB)

    Goldberg, A.; Lesuer, D.R.; Patt, J.

    1988-02-01

    Experimental results, together with an analytical model, related to the loss in tensile strength of styrene-butadiene rubber (SBR) loaded with carbon black (CB) that had been subjected to low-cycle, high-stress fatigue tests were presented in a prior paper. The drop in tensile strength relative to that of a virgin sample was considered to be a measure of damage induced during the fatigue test. The present paper is a continuation of this study dealing with the morphological interpretations of the fractured surfaces, whereby the cyclic-tearing behavior, resulting in the damage, is related to the test and material parameters. It was found that failure is almost always initiated in the bulk of a sample at a material flaw. The size and definition of a flaw increase with an increase in carbon-black loading. Initiation flaw sites are enveloped by fan-shaped or penny-shaped regions which develop during cycling. The size and morphology of a fatigue-tear region appears to be independent of the fatigue load or the extent of the damage (strength loss). By contrast, either an increase in cycling load or an increase in damage at constant load increases the definition of the fatigue-region morphology for all formulations of carbon-black. On the finest scale, the morphology can be described in terms of tearing of individual groups of rubber strands, collapsing to form a cell-like structure. 18 refs., 13 figs.

  11. Environmentally benign electroless nickel plating using supercritical carbon-dioxide on hydrophilically modified acrylonitrile-butadiene-styrene

    Science.gov (United States)

    Tengsuwan, Siwach; Ohshima, Masahiro

    2014-08-01

    Electroless Ni-P plating using supercritical carbon dioxide (scCO2) in conjunction with copolymer-based hydrophilic modification was applied to an acrylonitrile-butadiene-styrene (ABS) substrate. The surface of ABS substrate was hydrophilically modified by blending with a multi-block copolymer, poly(ether-ester-amide)s (PEEA), in injection molding process. The substrate was then impregnated with Pd(II)-hexafluoroacetylacetonate, Pd(hfa)2, using scCO2, followed by the electroless plating reaction. ABS/PEEA substrates with different PEEA to ABS blend ratios and different volume ratios of butadiene to the styrene-acrylonitrile copolymer (SAN) matrix were prepared to investigate how the dispersed PEEA and butadiene domains affected the blend morphology and the adhesive strength of the plating metal-to-polymer contact. Increasing the PEEA copolymer to ABS blend ratio increased the mass transfer rate of the plating solution in the ABS substrate. Consequently, the metal-polymer composite layer became thicker, which increased the adhesive strength of the metal-to-polymer contact because of the anchoring effect. The butadiene domains appeared to attract the Pd catalyst precursor, and thus, the proportion of butadiene in the ABS matrix also affected the adhesive strength of the contact between the metal layer and the substrate. The ABS substrate was successfully plated with a Ni-P metal layer with an average adhesive strength of 9.1 ± 0.5 N cm-1 by choosing appropriate ABS/PEEA blend ratios and a Pd(hfa)2 concentration.

  12. Preparing cellulose nanocrystal/acrylonitrile-butadiene-styrene nanocomposites using the master-batch method.

    Science.gov (United States)

    Ma, Libo; Zhang, Yang; Meng, Yujie; Anusonti-Inthra, Phuriwat; Wang, Siqun

    2015-07-10

    The master-batch method provides a simple way to apply cellulose nanocrystal (CNC) as reinforcement in a hydrophobic matrix. The two-stage process includes making high-CNC content (70 wt%) master batch pellets, then mixing acrylonitrile-butadiene-styrene (ABS) and maleic anhydride grafted polyethylene with the master batch pellets to prepare the ABS/CNC nanocomposite in extruder. SEM image indicates that self-assembled CNC nanosheets disperse evenly throughout the polymer matrix. The improved mechanical properties shown in tensile and DMA tests reveal that the CNC combines well with the ABS. TGA results show that the thermal degradation temperature of CNC in the master batch increases because of the protection of the ABS coating. This approach not only improves the dispersion ability and the thermal stability of CNC, but it is also applicable to use with other hydrophobic thermoplastics in industrial scale production. Copyright © 2015 Elsevier Ltd. All rights reserved.

  13. Thermal recycling of polystyrene and polystyrene-butadiene dissolved in a light cycle oil

    Energy Technology Data Exchange (ETDEWEB)

    Arandes, Jose M.; Erena, Javier; Olazar, Martin; Bilbao, Javier [Departamento de Ingenieria Quimica, Universidad del Pais Vasco, Apartado 644, 48080 Bilbao (Spain); Azkoiti, Miren J. [Departamento de Ingenieria Quimica y del Medio Ambiente, Universidad del Pais Vasco, Plaza de la Casilla 3, 48012 Bilbao (Spain)

    2003-12-01

    A study has been made of the cracking on a mesoporous silica of polystyrene (PS) and polystyrene-butadiene (PS-BD) dissolved in a light cycle oil (LCO) from a product stream of a commercial fluid catalytic cracking (FCC) unit. This study has been carried out in a reactor of short contact time (3 s) in the 723-823 K range. This strategy for simultaneous valorization of plastics and solvent avoids the technological problems inherent to the treatment of solid postconsumer-plastics and the limitation to heat transfer in the process of pyrolysis. The cracking of plastics has a synergistic effect on the conversion of LCO, as it contributes to increasing the yield of gasoline (C{sub 5}-C{sub 12}). The cracking of the PS/LCO blend produces high yields of styrene, whereas the cracking of the PS-BD/LCO blend produces a stream of products with petrochemical interest.

  14. Biodegradation behavior of styrene butadiene rubber (SBR) reinforced with modified coconut shell powder

    Science.gov (United States)

    Sreejith, M. P.; Balan, Aparna K.; Shaniba, V.; Jinitha, T. V.; Subair, N.; Purushothaman, E.

    2017-06-01

    Biodegradation behavior of styrene butadiene rubber composites reinforced with natural filler, coconut shell powder (CSP), with different filler loadings were carried out under soil burial conditions for three to six months. The extent of biodegradation of the composites was evaluated through weight loss, tensile strength and hardness measurements. It was observed that the permanence of the composites was remarkably dependent on filler modification, size of the filler particle and filler content. Composites containing silane modified filler were found to be more resistant to attack by the microbes present in the soil. Mechanical properties such as tensile strength, Young's modulus and hardness were decreased after soil burial testing due to the microbial attack onto the samples.

  15. Application of protective coatings from ultrahigh-molecular weight polyethylene to butadiene-nitrile rubber

    Science.gov (United States)

    Dyakonov, A. A.; Sokolova, M. D.; Shadrinov, N. V.; Sleptsova, S. A.

    2017-12-01

    The paper presents a method of applying a protective coating from ultrahigh molecular weight polyethylene to rubber products. A distinctive feature of the presented method is the prevulcanization of a rubber compound in order to form it into the desired shape and remove an excess rubber material. The application of an ultrahigh molecular weight polyethylene powder to the prepared surface ensures a uniform coating thickness. To achieve an optimal combination of rubber properties, we study how the scorch time affects its physical and mechanical properties, hardness, corrosion, abrasion and thermal resistance. We find the scorch time range in which a spatial elastomeric network forms that influences the penetration of ultrahigh molecular weight polyethylene into butadiene-nitrile rubber.

  16. 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.

  17. Low percolation threshold carbon-black/ nitrile-butadiene-rubber composites and their electromagnetic shielding effects.

    Science.gov (United States)

    Zeng, Min; Zhao, Dongliang; Yu, Ronghai; Feng, Meng; Yang, Bai; Liu, Xiaofang; Zhang, Yanghuan; Wang, Xinlin

    2013-02-01

    Nitrile-butadiene-rubber composites, filled with super conducting carbon black, are successfully prepared with low percolation threshold, high conductivity and electromagnetic shielding effectiveness. Percolation theory is used to represent the system's conductivity, and the corresponding result is close to the experimental value. The fitting curve also gives the weight fraction threshold and conductivity exponent of the conducting polymer. The percolation threshold of the composite is 9.2 phr, which is much smaller than previous homologous findings and lower than the value of short carbon fiber counterparts reported. The volume resistivity becomes 3.17 omega x cm for the 20 phr sample and decreases to 0.66 omega x cm for the 40 phr sample. At 1.8 GHz for 40 phr sample, the shielding effectiveness is -43 dB.

  18. Prediction of the Styrene Butadiene Rubber Performance by Emulsion Polymerization Using Backpropagation Neural Network

    Directory of Open Access Journals (Sweden)

    Yan-jiang Jin

    2013-01-01

    Full Text Available The effect of the amounts of initiator, emulsifier, and molecular weight regulator on the styrene butadiene rubber performance was investigated, based on the industrial original formula. It was found that the polymerization rate was increased with the increased dosage of initiator and emulsifier, and together with replenishing molecular weight regulator will make the Mooney viscosity of rubber meet the national standard when the conversion rate reaches 70%. The backpropagation neural network was trained by the original formula and ameliorated formula on the basis of Levenberg-Marquardt algorithm, and the relative error between the simulation results and experimental data is less than 1%. The good consistency shows that the BP neural network could predict the product performances in different formula conditions. It would pave the way for adjustment of the SBR formulation and prediction of the product performances.

  19. 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.

  20. Performance of asphaltic concrete incorporating styrene butadiene rubber subjected to varying aging condition

    Science.gov (United States)

    Salah, Faisal Mohammed; Jaya, Ramadhansyah Putra; Mohamed, Azman; Hassan, Norhidayah Abdul; Rosni, Nurul Najihah Mad; Mohamed, Abdullahi Ali; Agussabti

    2017-12-01

    The influence of styrene butadiene rubber (SBR) on asphaltic concrete properties at different aging conditions was presented in this study. These aging conditions were named as un-aged, short-term, and long-term aging. The conventional asphalt binder of penetration grade 60/70 was used in this work. Four different levels of SBR addition were employed (i.e., 0 %, 1 %, 3 %, and 5 % by binder weight). Asphalt concrete mixes were prepared at selected optimum asphalt content (5 %). The performance was evaluated based on Marshall Stability, resilient modulus, and dynamic creep tests. Results indicated the improving stability and permanent deformation characteristics that the mixes modified with SBR polymer have under aging conditions. The result also showed that the stability, resilient modulus, and dynamic creep tests have the highest rates compared to the short-term aging and un-aged samples. Thus, the use of 5 % SBR can produce more durable asphalt concrete mixtures with better serviceability.

  1. Morphological and mechanical properties of styrene butadiene rubber/nano copper nanocomposites

    Directory of Open Access Journals (Sweden)

    Maryam Hadizadeh Harandi

    Full Text Available In this research, rubber based nanocomposites with presence of nanoparticle has been studied. Styrene butadiene rubber (SBR/nanocopper (NC composites were prepared using two-roll mill method. Transmission electron microscope (TEM and scanning electron microscope (SEM images showed proper dispersion of NC in the SBR matrix without substantial agglomeration of nanoparticles. To evaluate the curing properties of nanocomposite samples, swelling and cure rheometric tests were conducted. Moreover, the rheological studies were carried out over a range of shear rates. The effect of NC particles was examined on the thermal behavior of the SBR using thermal gravimetric analysis (TGA. Furthermore, tensile tests were employed to investigate the capability of nanoparticles to enhance mechanical behavior of the compounds. The results showed enhancement in tensile properties with incorporation of NC to SBR matrix. Moreover, addition of NC increased shear viscosity and curing time of SBR composites. Keywords: Nanocopper, Rubber, Curing behavior, Rheological properties, Thermal stability, Tensile characteristics

  2. Effect of gamma irradiation on the properties of natural rubber/styrene butadiene rubber blends

    Directory of Open Access Journals (Sweden)

    A.B. Moustafa

    2016-09-01

    Full Text Available Blends of natural rubber (NR with styrene butadiene rubber (SBR with varying ratios have been prepared. Vulcanization of the prepared blends has been induced by irradiation of gamma rays with varying doses up to 250 kGy. Mechanical properties, namely tensile strength, tensile modulus at 100% elongation, elongation at break have been followed up as a function of irradiation dose as well as blend composition. Physical properties, namely gel fraction and swelling number have been followed up using benzene as a solvent. Thermal measurements namely thermogravimetric analysis were carried out. The results indicated that the addition of NR has improved the properties of NR / SBR blends. Also NR/SBR blend is thermally stable than NR alone.

  3. Microstructural analysis of carbon nanotubes produced from pyrolysis/combustion of styrene-butadiene rubber

    Energy Technology Data Exchange (ETDEWEB)

    Alves, Joner O.; Zhuo, Chuanwei; Levendis, Yannis A. [Northeastern Univ., Boston, MA (United States). Coll. of Engineering. Dept. of Mechanical and Industrial Engineering; Tenorio, Jorge A.S. [University of Sao Paulo (USP), SP (Brazil). Polytechnic School. Dept. of Metallurgical and Materials Engineering

    2010-07-01

    Styrene-Butadiene-Rubber (SBR) is a synthetic rubber copolymer used to fabricate several products. This study aims to demonstrate the use of SBR as feedstock for carbon nanotubes (CNTs) growth, and therefore to establish a novel process for destination for wastes produced from SBR. Pellets of this rubber were controlled burned at temperature of 1000 deg C, and a catalyst system was used to synthesize the nanomaterials. CNTs are materials with a wide range of potential applications due to their extraordinary mechanical, thermal and electrical properties. Produced materials were characterized by SEM and TEM, and the hydrocarbons emissions were measured using GC. Results showed that materials with diameters of 30-100 nm and lengths of about 30 {mu}m were formed. That materials presented similar structures of multi-walled CNTs. Therefore, the use of SBR to produce carbon nanotubes showed quite satisfactory and an interesting field for future investments. (author)

  4. The migration of acrylonitrile from acrylonitrile/butadiene/styrene polymers into food-simulating liquids.

    Science.gov (United States)

    Lickly, T D; Markham, D A; Rainey, M L

    1991-01-01

    The correlation of residual acrylonitrile (AN) monomer concentration in AN-containing polymers with AN migration into food simulants is of interest because the US FDA regulates the use of these polymers on the basis of the amount of AN that may migrate into food simulants. Studies of the migration of AN into water from seven acrylonitrile/butadiene/styrene polymers with varying composition and residual AN levels showed that a linear relationship exists between the concentration of AN in the polymer and the amount of AN migrating, for a given set of exposure conditions. A linear relationship was also observed between the diffusion coefficients generated from the experimental data using a simple Fickian diffusion model and the inverse of the absolute temperature of exposure.

  5. The influence of carbon black on curing kinetics and thermal aging of acrylonitrile–butadiene rubber

    Directory of Open Access Journals (Sweden)

    Jaroslava Budinski-Simendić

    2009-10-01

    Full Text Available Elastomers based on a copolymer of butadiene and acrylonitrile (NBR have excellent oil resistance but are very sensitive for degradation at very high temperatures. The aim of this applicative contribution was to determine the effect of high abrasion furnace carbon black with primary particle size 46 nm on aging properties of elastomeric materials based on NBR as network precursor. The curing kinetics was determined using the rheometer with an oscillating disk, in which the network formation process is registered by the torque variation during time. The vulcanizates were obtained in a hydraulic press at 150 °C. The mechanical properties of elastomeric composites were determined before and after thermal aging in an air circulating oven. The reinforcing effect of the filler particles was assessed according to mechanical properties before and after aging.

  6. 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.

  7. Tri-1-Methallyl- and 1-Methallyl-Butadiene Group IV Transition Metal Complexes

    OpenAIRE

    BLENKERS, J; Liefde Meijer, H.J. de; Teuben, J.H.

    1981-01-01

    Reaction of Cp´MCl3 (Cp´ = η5-C5(CH3)5; M = Ti, Zr, Hf) with 2-butenylmagnesium bromide at low temperatures gives Cp´M(1-methallyl)3, which is readily converted into Cp´M(η3-1-methallyl)(η4-butadiene) on heating. Only Cp´Hf(1 methallyl)3 could be isolated; it is fluxional and its NMR and IR spectra indicate that it consists of a complex mixture of isomers containing interconverting η1- and η3-1-methallyl groups. The compounds Cp´M(η3-C4H7)(η4-C4H6) are much more thermally stable; they show fl...

  8. Tensile, swelling and morphological properties of bentonite-filled acrylonitrile butadiene rubber composites

    Science.gov (United States)

    Lotfi, Muhamad Nadhli Amin; Ismail, Hanafi; Othman, Nadras

    2017-10-01

    Tensile, swelling and morphological properties of bentonite filled acrylonitrile butadiene rubber (NBR/Bt) composites were studied. The experiments were conducted at room temperature by using two rolled mill, universal testing machine (INSTRON), and American Standard Testing Method (ASTM) D471 for compounding, tensile testing, and swelling test, respectively. Results obtained indicated that a better tensile strength, elongation at break and tensile modulus were recorded as compared to the pure NBR particularly up to 90 phr of Bt loading. However, swelling (%) exhibited the opposite trend where the liquid uptake by the composites was indirectly proportional with the increasing of Bt loading. Scanning electron microscopy (SEM) used on the tensile fractured surface of the NBR/Bt composites have shown that the fillers were well embedded in the NBR matrix, for Bt loading up to 90 phr. The agglomeration of fillers occurred for Bt loading exceeding 90 phr.

  9. Anionic Polymerization of Styrene and 1,3-Butadiene in the Presence of Phosphazene Superbases

    KAUST Repository

    Ntetsikas, Konstantinos

    2017-10-23

    The anionic polymerization of styrene and 1,3-butadiene in the presence of phosphazene bases (t-BuP4, t-BuP2 and t-BuP1), in benzene at room temperature, was studied. When t-BuP1 was used, the polymerization proceeded in a controlled manner, whereas the obtained homopolymers exhibited the desired molecular weights and narrow polydispersity (Ð < 1.05). In the case of t-BuP2, homopolymers with higher than the theoretical molecular weights and relatively low polydispersity were obtained. On the other hand, in the presence of t-BuP4, the polymerization of styrene was uncontrolled due to the high reactivity of the formed carbanion. The kinetic studies from the polymerization of both monomers showed that the reaction rate follows the order of [t-BuP4]/[sec-BuLi] >>> [t-BuP2]/[sec-BuLi] >> [t-BuP1]/[sec-BuLi] > sec-BuLi. Furthermore, the addition of t-BuP2 and t-BuP1 prior the polymerization of 1,3-butadiene allowed the synthesis of polybutadiene with a high 1,2-microstructure (~45 wt %), due to the delocalization of the negative charge. Finally, the one pot synthesis of well-defined polyester-based copolymers [PS-b-PCL and PS-b-PLLA, PS: Polystyrene, PCL: Poly(ε-caprolactone) and PLLA: Poly(L-lactide)], with predictable molecular weights and a narrow molecular weight distribution (Ð < 1.2), was achieved by sequential copolymerization in the presence of t-BuP2 and t-BuP1.

  10. Dielectric study of Poly(styrene- co -butadiene) Composites with Carbon Black, Silica, and Nanoclay

    KAUST Repository

    Vo, Loan T.

    2011-08-09

    Dielectric spectroscopy is used to measure polymer relaxation in styrene-butadiene rubber (SBR) composites. In addition to the bulk polymer relaxation, the SBR nanocomposites also exhibit a slower relaxation attributed to polymer relaxation at the polymer-nanoparticle interface. The glass transition temperature associated with the slower relaxation is used as a way to quantify the interaction strength between the polymer and the surface. Comparisons were made among composites containing nanoclay, silica, and carbon black. The interfacial relaxation glass transition temperature of SBR-clay nanocomposites is more than 80 °C higher than the SBR bulk glass transition temperature. An interfacial mode was also observed for SBR-silica nanocomposites, but the interfacial glass transition temperature of SBR-silica nanocomposite is somewhat lower than that of clay nanocomposites. An interfacial mode is also seen in the carbon black filled system, but the signal is too weak to analyze quantitatively. The interfacial polymer relaxation in SBR-clay nanocomposites is stronger compared to both SBR-carbon black and SBR-silica composites indicating a stronger interfacial interaction in the nanocomposites containing clay. These results are consistent with dynamic shear rheology and dynamic mechanical analysis measurements showing a more pronounced reinforcement for the clay nanocomposites. Comparisons were also made among clay nanocomposites using different SBRs of varying styrene concentration and architecture. The interfacial glass transition temperature of SBR-clay nanocomposites increases as the amount of styrene in SBR increases indicating that styrene interacts more strongly than butadiene with clay. © 2011 American Chemical Society.

  11. Improved mechanical properties and ozone resistance of radiation-cured SBR. Final report, Dec 88-Jun 91. [Styrene Butadiene Rubber

    Energy Technology Data Exchange (ETDEWEB)

    Basfar, A.A.; Silverman, J.

    1991-08-01

    This report is a continuation and extension of the work of the earlier Army contract, where the superiority of the electron beam cured styrene butadiene rubber (SBR) tank pads to the sulfur cured pads was demonstrated. The focus of the present study is the investigation of the extraordinary ozone resistance of our radiation cured SBR, and also on possible alternatives for SBR, butadiene rubber (BR) in particular, as a tank pad compound. Base formulations of a fully sulfur cured system were established with 5% reproducibility, and results were confirmed by mechanical properties measurements on identical formulations from Belvoir Research Development and Engineering Center (BRDEC). Constant mechanical properties as a function of exposure to ozone indicate either competitive cross-linking and scissioning reactions or a 'protective' effect caused by higher terminal vinyl concentrations in the radiation cured formulations.

  12. Dominant lethal study in CD-1 mice following inhalation exposure to 1,3-butadiene: Final technical report

    Energy Technology Data Exchange (ETDEWEB)

    Hackett, P.L.; Mast, T.J.; Brown, M.G.; Clark, M.L.; Evanoff, J.J.; Rowe, S.E.; McClanahan, B.J.; Buschbom, R.L.; Decker, J.R.; Rommereim, R.L.; Westerberg, R.B.

    1988-04-01

    The effects of whole-body inhalation exposures to 1,3-butadiene on the reproductive system was evaluated. The results of dominant lethality in CD-1 male mice that were exposed to 1,3-butadiene are described. Subsequent to exposure, males were mated with two unexposed females. Mating was continued for 8 weeks with replacement of two females each week. Gravid uteri were removed, and the total number, position and status of implantations were determined. The mice were weighed prior to exposure and at 0, 1, 2, 3, 4, 5, 6, 7, and 8 weeks after exposure and at sacrifice. The animals were observed for mortality, morbidity and signs of toxicity throughout the study. 19 refs., 5 figs., 9 tabs.

  13. Thermomechanical properties of zirconium tungstate/hydrogenated nitrile butadiene rubber (HNBR) composites for low-temperature applications

    OpenAIRE

    Akulichev, Anton G.; Alcock, Ben; Tiwari, Avinash; Echtermeyer, Andreas T.

    2017-01-01

    Rubber compounds for pressure sealing application typically have inferior dimensional stability with temperature fluctuations compared with their steel counterparts. This effect may result in seal leakage failures when subjected to decreases in temperature. Composites of hydrogenated nitrile butadiene rubber (HNBR) and zirconium tungstate as a negative thermal expansion filler were prepared in order to control the thermal expansivity of the material. The amount of zirconium tungstate (ZrW2O8)...

  14. Personal exposure to benzene and 1,3-butadiene during petroleum refinery turnarounds and work in the oil harbour.

    Science.gov (United States)

    Akerstrom, M; Almerud, P; Andersson, E M; Strandberg, B; Sallsten, G

    2016-11-01

    Petroleum refinery workers' exposure to the carcinogens benzene and 1,3-butadiene has decreased during normal operations. However, certain occupational groups or events at the refineries still involve a risk of higher exposures. The aim of this study was to examine the personal exposure to benzene and 1,3-butadiene at refinery turnarounds and during work in the oil harbour. Personal exposure measurements of benzene and 1,3-butadiene were taken during work shifts, with a priori assumed higher benzene exposure, using PerkinElmer diffusive samplers filled with Carbopack X. Mean exposure levels were calculated, and repeated exposure measurements, when available, were assessed using mixed effect models. Group and individual compliance with the Swedish occupational exposure limit (OEL) was tested for the different exposure groups. Mean benzene exposure levels for refinery workers during the three measured turnarounds were 150, 610 and 960 µg/m(3), and mean exposures for oil harbour workers and sewage tanker drivers were 310 and 360 µg/m(3), respectively. Higher exposures were associated with handling benzene-rich products. Most occupational groups did not comply with the Swedish OEL for benzene nor did the individuals within the groups. The exposure to 1,3-butadiene was very low, between refinery industry, with potential exposure to open product streams containing higher fractions of benzene, pose a risk of personal benzene exposures exceeding the OEL. Refinery workers performing these work tasks frequently, such as contractors, sewage tanker drivers and oil harbour workers, need to be identified and protected.

  15. Morphology and Dynamic Mechanical Properties of Diglycidyl Ether of Bisphenol-A Toughened with Carboxyl-Terminated Butadiene-Acrylonitrile

    Science.gov (United States)

    Hong, S. D.; Chung, S. Y.; Fedors, R. F.; Moacanin, J.; Gupta, A.

    1984-01-01

    The fracture toughness of an incorporation of a carboxyl-terminated butadiene acrylonitrile (CTBN) elastomer in diglycidyl ether bisphenol A (DGEBA) resin was investigated. Measurements of dynamic mechanical properties, scanning electron microscopy and small-angle X-ray scattering were carried out to characterize the state of cure, morphology and particle size and size distribution of the neat resins and their graphite fiber reinforced composites.

  16. Effect of concentration and humidity on the formation of porous polymer films using Styrene Butadiene Co-Polymer

    Science.gov (United States)

    Jose, Renu; Sujith, A.; Predeep, P.

    2011-10-01

    Honeycomb structured porous materials from complex polymers are formed using water droplet templating method. In the present work microporous films were prepared from styrene butadiene rubber (SBR) using emulsion technique. The pore sizes can be easily tuned by changing the concentration and the humidity condition. The pore size is characterized by optical microscope and Scanning electron microscope (SEM). These films can be used for various applications in optoelectronics, photonics, catalysis, tissue engineering, bioanalytical purposes etc.

  17. Study of the thermal properties of Acrylonitrile Butadiene Styrene - High Impact Polystyrene blends with Styrene Ethylene Butylene Styrene

    OpenAIRE

    PEYDRO Miguel Angel; JUAREZ David; Sanchez-Caballero, Samuel; PARRES Francisco

    2013-01-01

    A binary blend Acrylonitrile Butadiene Styrene ¿ High Impact Polystyrene (ABS-HIPS 50% wt) was prepared on a twin-screw extruder at 190-210 oC. The different properties were then analyzed using melt flow index (MFI), thermogravimetric analysis (TGA), and Fourier Transform Infrared spectroscopy (FTIR). FTIR analysis indicated heterogeneous distribution of the blend in injected pieces and SEM micrographs show heterogeneous distribution of both phase (ABS and HIPS). On the other hand, we have pr...

  18. 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.

  19. Ag-Promoted ZrBEA Zeolites Obtained by Post-Synthetic Modification for Conversion of Ethanol to Butadiene.

    Science.gov (United States)

    Sushkevich, Vitaly L; Ivanova, Irina I

    2016-08-23

    1,3-Butadiene was synthesized from ethanol using zirconium-containing zeolite beta (ZrBEA) catalysts doped with 1 wt % silver. The Zr was planted using post-synthesis modification by dealumination of the parent zeolite followed by treatment with ZrOCl2 in a DMSO solution. FTIR and NMR spectroscopy were used to investigate the planting process by preparing materials with different Si/Al ratios and crystal sizes. The results showed preferential grafting of Zr to the terminal silanols present on the external surface of the zeolite crystals instead of incorporation of Zr into silanol nests. The grafting yielded highly accessible Zr(OSi)3 OH open sites with high Lewis acidity, as confirmed by FTIR spectroscopy of adsorbed CO. These sites are shown to be extremely active for the conversion of ethanol to butadiene. Ag/ZrBEA catalysts prepared using the post-synthesis method showed significant advantages compared with Ag/ZrBEA catalysts synthesized using a conventional hydrothermal procedure. The best catalyst performance in terms of butadiene formation rate (3 μmol g(-1)  s(-1) ) was observed over Ag/Zr(3.5)BEA(75) (containing 3.5 wt % Zr), which had the smallest crystal size and the highest content of Zr open sites of the prepared catalysts. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  20. Integrated techno-economic and environmental analysis of butadiene production from biomass.

    Science.gov (United States)

    Farzad, Somayeh; Mandegari, Mohsen Ali; Görgens, Johann F

    2017-09-01

    In this study, lignocellulose biorefineries annexed to a typical sugar mill were investigated to produce either ethanol (EtOH) or 1,3-butadiene (BD), utilizing bagasse and trash as feedstock. Aspen simulation of the scenarios were developed and evaluated in terms of economic and environmental performance. The minimum selling prices (MSPs) for bio-based BD and EtOH production were 2.9-3.3 and 1.26-1.38-fold higher than market prices, respectively. Based on the sensitivity analysis results, capital investment, Internal Rate of Return and extension of annual operating time had the greatest impact on the MSP. Monte Carlo simulation demonstrated that EtOH and BD productions could be profitable if the average of ten-year historical price increases by 1.05 and 1.9-fold, respectively. The fossil-based route was found inferior to bio-based pathway across all investigated environmental impact categories, due to burdens associated with oil extraction. Copyright © 2017 Elsevier Ltd. All rights reserved.

  1. Experimental acrylonitrile butadiene styrene and polyamide evisceration implant: a rabbit clinical and histopathology study

    Directory of Open Access Journals (Sweden)

    D.C. Gomes Júnior

    Full Text Available ABSTRACT The purpose of this study was to evaluate acrylonitrile butadiene styrene (ABS and polyamide implants in rabbits submitted to evisceration at the macroscopic and microstructure level and to assess clinical response and histopathological changes as well. For the experimental study implants of 12mm diameter were prepared by rapid prototyping, weighed and the outer and inner surfaces evaluated macroscopically and by electron microscopy. In addition, a compression test was performed and ultrastructural damage was then determined. After evisceration of the left eyeball, nine New Zealand rabbits received ABS implants and nine others received polyamide implants. The animals were assessed daily for 15 days after surgery and every seven days until the end of the study (90 days. Histopathological evaluation was performed at 15, 45 and 90 days after surgery. The ABS implants weighed approximately 0.44g, while the polyamide ones weighed 0.61g. Scanning electron microscopy demonstrated that the ABS implants had regular-sized, equidistant micropores, while the polyamide ones showed micropores of various sizes. The force required to fracture the ABS implant was 14.39 ±0.60 Mpa, while for the polyamide one, it was 16.80 ±1.05 Mpa. Fifteen days after surgery, we observed centripetal tissue infiltration and scarce inflammatory infiltrate. Implants may be used in the filling of anophthalmic cavities, because they are inert, biocompatible and allow tissue integration.

  2. Mechanical and Thermal Properties of Styrene Butadiene Rubber - Functionalized Carbon Nanotubes Nanocomposites

    KAUST Repository

    Laoui, Tahar

    2013-01-01

    The effect of reinforcing styrene butadiene rubber (SBR) with functionalized carbon nanotubes on the mechanical and thermal properties of the nanocomposite was investigated. Multi-walled carbon nanotubes (CNTs) were functionalized with phenol functional group to enhance their dispersion in SBR matrix. Surface functionalization of the CNTs was carried out using acid treatment and FTIR technique was utilized so as to ascertain the presence of phenol functional group. This was followed with the dispersion of the functionalized CNTs into a polymer solution and a subsequent evaporation of the solvent. This study has demonstrated the inherent capability of CNTs as reinforcing filler as demonstrated by the substantial improvement in Young\\'s Modulus, tensile strength and energy of absorption of the nanocomposites. The tensile strength increased from 0.17 MPa (SBR) to 0.48 MPa while the Young\\'s Modulus increased from 0.25 MPa to 0.83 MPa when 10wt% functionalized CNTs was added. With the addition of 1wt% reinforcement-a peak value of 4.1 KJ energy absorption was obtained. The homogenous dispersion of CNT-Phenol is thought to be responsible for the considerable enhancement in the reported properties. Copyright © Taylor & Francis Group, LLC.

  3. 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.

  4. Tensile, Creep, and Fatigue Behaviors of 3D-Printed Acrylonitrile Butadiene Styrene

    Science.gov (United States)

    Zhang, Hanyin; Cai, Linlin; Golub, Michael; Zhang, Yi; Yang, Xuehui; Schlarman, Kate; Zhang, Jing

    2018-01-01

    Acrylonitrile butadiene styrene (ABS) is a widely used thermoplastics in 3D printing. However, there is a lack of thorough investigation of the mechanical properties of 3D-printed ABS components, including orientation-dependent tensile strength and creep fatigue properties. In this work, a systematic characterization is conducted on the mechanical properties of 3D-printed ABS components. Specifically, the effect of printing orientation on the tensile and creep properties is investigated. The results show that, in tensile tests, the 0° printing orientation has the highest Young's modulus of 1.81 GPa, and ultimate strength of 224 MPa. In the creep test, the 90° printing orientation has the lowest k value of 0.2 in the plastics creep model, suggesting 90° is the most creep resistant direction. In the fatigue test, the average cycle number under load of 30 N is 3796 cycles. The average cycle number decreases to 128 cycles when the load is 60 N. Using the Paris law, with an estimated crack size of 0.75 mm, and stress intensity factor is varied from 352 to 700 N√ m, the derived fatigue crack growth rate is 0.0341 mm/cycle. This study provides important mechanical property data that is useful for applying 3D-printed ABS in engineering applications.

  5. Thermal Stability and Flammability of Styrene-Butadiene Rubber-Based (SBR Ceramifiable Composites

    Directory of Open Access Journals (Sweden)

    Rafał Anyszka

    2016-07-01

    Full Text Available Ceramifiable styrene-butadiene (SBR-based composites containing low-softening-point-temperature glassy frit promoting ceramification, precipitated silica, one of four thermally stable refractory fillers (halloysite, calcined kaolin, mica or wollastonite and a sulfur-based curing system were prepared. Kinetics of vulcanization and basic mechanical properties were analyzed and added as Supplementary Materials. Combustibility of the composites was measured by means of cone calorimetry. Their thermal properties were analyzed by means of thermogravimetry and specific heat capacity determination. Activation energy of thermal decomposition was calculated using the Flynn-Wall-Ozawa method. Finally, compression strength of the composites after ceramification was measured and their micromorphology was studied by scanning electron microscopy. The addition of a ceramification-facilitating system resulted in the lowering of combustibility and significant improvement of the thermal stability of the composites. Moreover, the compression strength of the mineral structure formed after ceramification is considerably high. The most promising refractory fillers for SBR-based ceramifiable composites are mica and halloysite.

  6. Tensile, Creep, and Fatigue Behaviors of 3D-Printed Acrylonitrile Butadiene Styrene

    Science.gov (United States)

    Zhang, Hanyin; Cai, Linlin; Golub, Michael; Zhang, Yi; Yang, Xuehui; Schlarman, Kate; Zhang, Jing

    2017-09-01

    Acrylonitrile butadiene styrene (ABS) is a widely used thermoplastics in 3D printing. However, there is a lack of thorough investigation of the mechanical properties of 3D-printed ABS components, including orientation-dependent tensile strength and creep fatigue properties. In this work, a systematic characterization is conducted on the mechanical properties of 3D-printed ABS components. Specifically, the effect of printing orientation on the tensile and creep properties is investigated. The results show that, in tensile tests, the 0° printing orientation has the highest Young's modulus of 1.81 GPa, and ultimate strength of 224 MPa. In the creep test, the 90° printing orientation has the lowest k value of 0.2 in the plastics creep model, suggesting 90° is the most creep resistant direction. In the fatigue test, the average cycle number under load of 30 N is 3796 cycles. The average cycle number decreases to 128 cycles when the load is 60 N. Using the Paris law, with an estimated crack size of 0.75 mm, and stress intensity factor is varied from 352 to 700 N√ m , the derived fatigue crack growth rate is 0.0341 mm/cycle. This study provides important mechanical property data that is useful for applying 3D-printed ABS in engineering applications.

  7. Natural rubber/nitrile butadiene rubber/hindered phenol composites with high-damping properties

    Directory of Open Access Journals (Sweden)

    Xiuying Zhao

    2015-10-01

    Full Text Available New natural rubber (NR/nitrile butadiene rubber (NBR/hindered phenol (AO-80 composites with high-damping properties were prepared in this study. The morphological, structural, and mechanical properties were characterized by atomic force microscopy (AFM, polarized Fourier transform infrared spectrometer (FTIR, dynamic mechanical thermal analyzer (DMTA, and a tensile tester. Each composite consisted of two phases: the NR phase and the NBR/AO-80 phase. There was partial compatibility between the NR phase and the NBR/AO-80 phase, and the NR/NBR/AO-80 (50/50/20 composite exhibited a co-continuous morphology. Strain-induced crystallization occurred in the NR phase at strains higher than 200%, and strain-induced orientation appeared in the NBR/AO-80 phase with the increase of strain from 100% to 500%. The composites had a special stress–strain behavior and mechanical properties because of the simultaneous strain-induced orientation and strain-induced crystallization. In the working temperature range of a seismic isolation bearing, the composites (especially the NR/NBR/AO-80 (50/50/20 composite presented a high loss factor, high area of loss peak (TA, and high hysteresis energy. Therefore, the NR/NBR/AO-80 rubber composites are expected to have important application as a high-performance damping material for rubber bearing.

  8. Styrene-butadiene rubber/halloysite nanotubes nanocomposites modified by methacrylic acid

    Energy Technology Data Exchange (ETDEWEB)

    Guo Baochun [Department of Polymer Materials and Engineering, South China University of Technology, Guangzhou 510640 (China)], E-mail: psbcguo@scut.edu.cn; Lei Yanda; Chen Feng; Liu Xiaoliang; Du Mingliang; Jia Demin [Department of Polymer Materials and Engineering, South China University of Technology, Guangzhou 510640 (China)

    2008-12-30

    Methacrylic acid (MAA) was used to improve the performance of styrene-butadiene rubber (SBR)/halloysite nanotubes (HNTs) nanocomposites by direct blending. The detailed interaction mechanisms of MAA and the in situ formed zinc methacrylate (ZDMA) were revealed by X-ray diffraction (XRD), surface area and porosity analysis, X-ray photoelectron spectroscopy (XPS) together with crosslink density determination. The strong interfacial bonding between HNTs and rubber matrix is resulted through ZDMA and MAA intermediated linkages. ZDMA connects SBR and HNTs via grafting/complexation mechanism. MAA bonds SBR and HNTs through grafting/hydrogen bonding mechanism. Significantly improved dispersion of HNTs in virtue of the interactions between HNTs and MAA or ZDMA was achieved. Effects of MAA content on the vulcanization behavior, morphology and mechanical properties of the nanocomposites were investigated. Promising mechanical properties of MAA modified SBR/HNTs nanocomposites were obtained. The changes in vulcanization behavior, mechanical properties and morphology were correlated with the interactions between HNTs and MAA or ZDMA and the largely improved dispersion of HNTs.

  9. Thermal Stability and Flammability of Styrene-Butadiene Rubber-Based (SBR) Ceramifiable Composites

    Science.gov (United States)

    Anyszka, Rafał; Bieliński, Dariusz M.; Pędzich, Zbigniew; Rybiński, Przemysław; Imiela, Mateusz; Siciński, Mariusz; Zarzecka-Napierała, Magdalena; Gozdek, Tomasz; Rutkowski, Paweł

    2016-01-01

    Ceramifiable styrene-butadiene (SBR)-based composites containing low-softening-point-temperature glassy frit promoting ceramification, precipitated silica, one of four thermally stable refractory fillers (halloysite, calcined kaolin, mica or wollastonite) and a sulfur-based curing system were prepared. Kinetics of vulcanization and basic mechanical properties were analyzed and added as Supplementary Materials. Combustibility of the composites was measured by means of cone calorimetry. Their thermal properties were analyzed by means of thermogravimetry and specific heat capacity determination. Activation energy of thermal decomposition was calculated using the Flynn-Wall-Ozawa method. Finally, compression strength of the composites after ceramification was measured and their micromorphology was studied by scanning electron microscopy. The addition of a ceramification-facilitating system resulted in the lowering of combustibility and significant improvement of the thermal stability of the composites. Moreover, the compression strength of the mineral structure formed after ceramification is considerably high. The most promising refractory fillers for SBR-based ceramifiable composites are mica and halloysite. PMID:28773726

  10. About the cure kinetics in natural rubber/styrene Butadiene rubber blends at 433 K

    Energy Technology Data Exchange (ETDEWEB)

    Mansilla, M.A., E-mail: mmansilla@df.uba.ar [Laboratorio de Polimeros y Materiales Compuestos, Departamento de Fisica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pabellon 1, C1428EGA Buenos Aires (Argentina); Marzocca, A.J. [Laboratorio de Polimeros y Materiales Compuestos, Departamento de Fisica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pabellon 1, C1428EGA Buenos Aires (Argentina)

    2012-08-15

    Vulcanized blends of elastomers are employed in several goods mainly to improve physical properties and reduce costs. One of the most used blends of this kind is that composed by natural rubber (NR) and styrene butadiene rubber (SBR). The cure kinetic of these blends depends mainly on the compound formulation and the cure temperature and time. The preparation method of the blends can influence the mechanical properties of the vulcanized compounds. In this work the cure kinetic at 433 K of NR/SBR blends vulcanized with the system sulfur/TBBS (N-t-butyl-2-benzothiazole sulfenamide) is analyzed in samples prepared by mechanical mixing and solution blending. The two methods produce elastomer domains of NR and SBR, which present different microstructure due to the cure level attained during vulcanization. The cure kinetics is studied by means of rheometer tests and the model proposed by Kamal and Sourour. The analysis of the cure rate is presented and is related to the structure obtained during the vulcanization process.

  11. Novel blends of acrylonitrile butadiene rubber and polyurethane-silica hybrid networks

    Directory of Open Access Journals (Sweden)

    X. P. Wang

    2012-07-01

    Full Text Available Novel blends of acrylonitrile butadiene rubber (NBR and polyurethane-silica (PU-SiO2 hybrid networks have been prepared by melt blending. The PU-SiO2 hybrid networks were formed via the reaction of NCO groups of NCO-terminated PU prepolymer and OH groups of SiO2 in the absence of an external crosslinking agent (i.e. alcohols and amines during the curing process of NBR. Both in the neat PU-SiO2 system and the NBR/(PU-SiO2 system, the NCO-terminated PU prepolymer could be crosslinked by SiO2 to form PU-SiO2 hybrid networks. The effects of PU-SiO2 introduction into the NBR, on the properties of the resulting blends were studied. It was found that the vulcanization was activated by the incorporation of PU-SiO2. Transmission electronic microscopy (TEM studies indicated that the interpenetration and entanglement structures between NBR and PU-SiO2 increased with increasing PU-SiO2 content and the quasi-interpenetrating polymer networks (quasi-IPN structures were formed when the PU-SiO2 was 50 wt% in the NBR/(PU-SiO2 systems. The microstructures formed in the blends led to good compatibility between NBR and PU-SiO2 and significantly improved the mechanical properties, abrasion resistance and flex-fatigue life of the blends.

  12. Zinc chelates as new activators for sulphur vulcanization of acrylonitrile-butadiene elastomer

    Directory of Open Access Journals (Sweden)

    2009-04-01

    Full Text Available The goal of this work was to apply several zinc chelates as activators for sulphur vulcanization of acrylonitrilebutadiene elastomer (NBR, in order to find alternatives for the conventionally used zinc oxide. In this article, we discuss the effects of different zinc complexes on the cure characteristics, crosslinks distribution in the elastomer network and mechanical properties of acrylonitrile-butadiene rubber. Zinc chelates seem to be good substitutes for zinc oxide as activators for sulphur vulcanization of NBR rubber, without detrimental effects on the crosslinking process and physical properties of the obtained vulcanizates. Moreover, application of zinc complexes allows to reduce the amount of zinc ions in rubber compounds by 40% compared to conventionally crosslinked vulcanizates with zinc oxide. It is a very important ecological goal since zinc oxide is classified as toxic to aquatic species and its amount in rubber products must be reduced below 2.5% at least. From a technological point of view it is a very important challenge.

  13. Devulcanization of styrene butadiene rubber by microwave energy: Effect of the presence of ionic liquid

    Directory of Open Access Journals (Sweden)

    S. Seghar

    2015-12-01

    Full Text Available In this study, styrene butadiene rubber (SBR was devulcanized using microwave irradiation. In particular, effect of ionic liquid (IL, pyrrolidinium hydrogen sulfate [Pyrr][HSO4], on the devulcanization performance was studied. It was observed that the evolution of the temperature reached by rubber powder exposed to microwave irradiation for different energy values was favored by the presence of ionic liquid [Pyrr][HSO4] significantly over the whole range of the microwave energy values. Beyond the threshold point of 220 Wh/kg, the soluble fraction after devulcanization sharply increased with increasing devulcanization microwave energy. For the powder mixed with [Pyrr][HSO4], the increase was more significant. Furthermore, the crosslink density was observed to decrease slowly with the microwave energy up to 220 Wh/kg, beyond which the crosslink density decreased significantly for the rubber impregnated with IL. For the rubber with IL, significant and continuous increase in Tg with microwave energy values was observed in comparison with the SBR where no change in transition temperature was observed. Mechanical shearing of rubber gums in the two-roll mill favored the devulcanization process, which indicated that the combination of mechanical loading with microwave energy and IL is an efficient procedure allowing an optimal devulcanization of rubbers.

  14. Microstructural analysis of carbon nanomaterials produced from pyrolysis/combustion of Styrene-Butadiene-Rubber (SBR

    Directory of Open Access Journals (Sweden)

    Joner Oliveira Alves

    2011-12-01

    Full Text Available Styrene-Butadiene-Rubber (SBR is a synthetic rubber copolymer used to fabricate several products. This study aims to demonstrate the use of SBR as feedstock for carbon nanomaterials (nanofibers and nanotubes growth, and therefore to establish a novel process for destination of waste products containing SBR. A three stage electrically heated flow reactor was used. Small pellets of rubber were pyrolyzed at a temperature of 1000 ºC. The pyrolyzates were mixed with oxygen-containing gases and were burned. The products of combustion were used to synthesize the carbon nanomaterials (CNMs at the presence of a catalyst. CNMs have a wide range of potential applications due to their extraordinary mechanical, thermal and electrical properties. Produced materials were characterized by SEM and TEM, whereas combustion products were assessed using GC. Results showed that CNMs with outer diameters of 30-100 nm and lengths of about 30 µm were formed. Therefore, it was demonstrated that waste products containing SBR can be used to generate CNMs which are value-added products of intense technological interest.

  15. Application of Composite Powders Recycled from Graphite Tailings in Styrene-Butadiene Rubber

    Science.gov (United States)

    Hai, Yun; Liao, Libing; Lv, Guocheng; Qin, Faxiang; Mei, Lefu; Wei, Yaozu

    2015-11-01

    With styrene-butadiene rubber (SBR) as matrix and composite powders recycled from graphite tailings as fillers, the influence of the particle size and content of the composite powders on the tensile strength and electrical conductivity of the composite powder-filled SBR were studied. The results showed that composite powder recycled from graphite tailings could reinforce SBR, whose tensile strength was significantly increased with reducing the particle size of the composite powder, but it had little effect on the conductivity of the system. With composite powders as fillers in conjunction with conductive carbon black, the tensile strength and electrical conductivity of the system were greatly improved. The maximum tensile strength of the SBR filled with composite powder and conductive carbon black increased by 47% compared to that of the single composite powder-filled SBR. When the filling content of conductive carbon black was 10 phr and that of composite powder was above 30 phr, the volume resistivity of SBR showed a sharp decline, reaching a minimum about 106 Ω cm at 40 phr. All the results indicated that composite powder recycled from graphite tailings can be applied effectively as filler in SBR. It has great economic and environmental benefits.

  16. Performance of Styrene Butadiene Rubber as a Concrete Repair Material in tropical climate

    Science.gov (United States)

    Radhakrishnan, R.; Prakash, V. Syam; Thampan, C. K.; Varma, Prasad

    2012-11-01

    Deterioration of Concrete due to variety of reasons like corrosion of steel, inferior quality of materials as well as workmanship and exposure to aggressive environment like thermal cycling affect the performance or damage a number of Reinforced cement concrete structures. In order to repair these structures for enhancing the service life, number of methods and materials are available. But the degree of success of any repair in concrete depends mainly on the correct choice and the method of application of repair materials. This paper discusses the details of an experimental investigation on the performance of Styrene ñ Butadiene Rubber (SBR) as a concrete repair material in tropical climatic conditions. Resistance to water penetration and tensile cracking are two important performance criteria for any repair material. Cement mortar cubes of mix proportion 1:3 with SBR added at the rate of 20% of the weight of cement, and control specimens without SBR were made. Compressive strength and sorptivity values of the cubes were determined. Shear Bond strength (by slant shear test) and splitting tensile strength of the repaired cylinder specimens of standard dimensions, in which SBR used as a bonding agent were determined. These values were compared with the values obtained for the similar specimens, in which the bonding agent applied was conventional cement slurry. The influence of thermal cycling on the properties of repaired concrete specimens were also studied. A comparison has also been made with the values required to meet the standard specifications of a repair material.

  17. Functionalized Nanochannels from Self-Assembled and Photomodified Poly(Styrene-b-Butadiene-b-Styrene).

    Science.gov (United States)

    Sutisna, Burhannudin; Polymeropoulos, George; Musteata, Valentina; Sougrat, Rachid; Smilgies, Detlef-M; Peinemann, Klaus-Viktor; Hadjichristidis, Nikolaos; Nunes, Suzana P

    2017-10-04

    Membranes are prepared by self-assembly and casting of 5 and 13 wt% poly(styrene-b-butadiene-b-styrene) (PS-b-PB-b-PS) copolymers solutions in different solvents, followed by immersion in water or ethanol. By controlling the solution-casting gap, porous films of 50 and 1 µm thickness are obtained. A gradient of increasing pore size is generated as the distance from the surface increased. An ordered porous surface layer with continuous nanochannels can be observed. Its formation is investigated, by using time-resolved grazing incident small angle X-ray scattering, electron microscopy, and rheology, suggesting a strong effect of the air-solution interface on the morphology formation. The thin PS-b-PB-b-PS ordered films are modified, by promoting the photolytic addition of thioglycolic acid to the polybutadiene groups, adding chemical functionality and specific transport characteristics on the preformed nanochannels, without sacrificing the membrane morphology. Photomodification increases fivefold the water permeance to around 2 L m(-2) h(-1) bar(-1) , compared to that of the unmodified one. A rejection of 74% is measured for methyl orange in water. The membranes fabrication with tailored nanochannels and chemical functionalities can be demonstrated using relatively lower cost block copolymers. Casting on porous polyacrylonitrile supports makes the membranes even more scalable and competitive in large scale. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Carbon nanotube buckypaper reinforced acrylonitrile-butadiene-styrene composites for electronic applications.

    Science.gov (United States)

    Díez-Pascual, Ana M; Gascón, David

    2013-11-27

    Novel acrylonitrile-butadiene-styrene (ABS) nanocomposites reinforced with pristine or functionalized single- or multiwalled carbon nanotube buckypaper (BP) sheets were manufactured via hot-compression and vacuum infiltration. Their morphology, thermal, mechanical, and electrical properties were comparatively investigated. Scanning electron microscopy and thermogravimetric analysis showed that the infiltration process leads to better BP impregnation than the hot-press technique. BPs made from functionalized or short nanotubes form compact networks that hamper the penetration of the matrix chains, whereas those composed of pristine tubes possess large pores that facilitate the polymer flow, resulting in composites with low degree of porosity and improved mechanical performance. Enhanced thermal and electrical properties are found for samples incorporating functionalized BPs since dense networks lead to more conductive pathways, and a stronger barrier effect to the diffusion of degradation products, thus better thermal stability. According to dynamic mechanical analysis these composites exhibit the highest glass transition temperatures, suggesting enhanced filler-matrix interactions as corroborated by the Raman spectra. The results presented herein demonstrate that the composite performance can be tailored by controlling the BP architecture and offer useful insights into the structure-property relationships of these materials to be used in electronic applications, particularly for EMI shielding and packaging of integrated circuits.

  19. Olfactory loss in poly (acrylonitrile-butadiene-styrene) plastic injection-moulding workers.

    Science.gov (United States)

    Cheng, Shu-Fang; Chen, Mei-Lien; Hung, Po-Chen; Chen, Chiou-Jong; Mao, I-Fang

    2004-10-01

    Plastics manufacturing factories are the fifth largest category of factories in industrial estates in Taiwan. It is known that complex airborne compounds and pungent odours are emitted during plastic injection-moulding processes. Workers exposed to acrylonitrile-butadiene-styrene (ABS) thermal decomposition products (TDP) may have olfactory loss. This study examined olfactory loss in injection-moulding workers exposed to ABS TDP. The method recommended by the Connecticut Chemosensory Clinical Research Center (CCCRC) was used to test the olfactory function of subjects, including 1-butanol threshold and odour identification, both pre- and post-work. The study sample included 52 ABS plastic injection-moulding workers (exposed group), as well as 72 workers from other departments (reference group). The results revealed that the exposed group had lower olfactory function after work than the reference group. The decrease in olfactory function after 1 workday was statistically significant. The prevalence of abnormal olfactory function post-work in the exposed group was higher than in the reference group. The findings of this study implied the ABS plastic injection-moulding process may worsen olfactory function among workers. Notably, this effect decreased olfactory threshold scores, not odour identification scores.

  20. Crack initiation and propagation on the polymeric material ABS (Acrylonitrile Butadiene Styrene, under ultrasonic fatigue testing

    Directory of Open Access Journals (Sweden)

    G. M. Domínguez Almaraz

    2015-10-01

    Full Text Available Crack initiation and propagation have been investigated on the polymeric material ABS (Acrylonitrile Butadiene Styrene, under ultrasonic fatigue testing. Three controlled actions were implemented in order to carry out fatigue tests at very high frequency on this material of low thermal conductivity, they are: a The applying load was low to limit heat dissipation at the specimen neck section, b The dimensions of testing specimen were small (but fitting the resonance condition, in order to restraint the temperature gradient at the specimen narrow section, c Temperature at the specimen neck section was restrained by immersion in water or oil during ultrasonic fatigue testing. Experimental results are discussed on the basis of thermo-mechanical behaviour: the tail phenomenon at the initial stage of fatigue, initial shear yielding deformation, crazed development on the later stage, plastic strain on the fracture surface and the transition from low to high crack growth rate. In addition, a numerical analysis is developed to evaluate the J integral of energy dissipation and the stress intensity factor K, with the crack length

  1. Biological monitoring to determine worker dose in a butadiene processing plant

    Energy Technology Data Exchange (ETDEWEB)

    Bechtold, W.E.; Hayes, R.B. [National Cancer Inst., Bethesda, MD (United States)

    1995-12-01

    Butadiene (BD) is a reactive gas used extensively in the rubber industry and is also found in combustion products. Although BD is genotoxic and acts as an animal carcinogen, the evidence for carcinogenicity in humans is limited. Extrapolation from animal studies on BD carcinogenicity to risk in humans has been controversial because of uncertainties regarding relative biologic exposure and related effects in humans vs. experimental animals. To reduce this uncertainty, a study was designed to characterize exposure to BD at a polymer production facility and to relate this exposure to mutational and cytogenetic effects. Biological monitoring was used to better assess the internal dose of BD received by the workers. Measurement of 1,2-dihydroxy-4-(N-acetylcysteinyl) butane (M1) in urine served as the biomarker in this study. M1 has been shown to correlate with area monitoring in previous studies. Most studies that relate exposure to a toxic chemical with its biological effects rely on exposure concentration as the dose metric; however, exposure concentration may or may not reflect the actual internal dose of the chemical.

  2. SYNTHESIS AND PHARMACOLOGICAL EFFECTS OF BUTADIENE AND CYCLOPENTADIENE ADDUCTS OF METHANDROSTENOLONE IN RATS

    Directory of Open Access Journals (Sweden)

    FAZEL SHAMSA

    2006-06-01

    Full Text Available In this study the reactivity of methandrostenolone or [(17b-17-hydroxy-17-methylandrosta-1, 4-diene-3-one], as a dienophil in a Diels-Alder type cycloaddition reaction was investigated. The purpose of this approach was to investigate whether the 1-dehydro position of methandrostenolone 1 undergoes a cycloaddition reaction with dienes, such as 1, 3 butadiene or cyclopentadiene, and to investigate the biological behavior of the reaction adducts, i.e, compound 3 {(17b-17-hydroxy-17-methyl androsta [1a, 2a] cyclohex 3’, 4-diene-3-one} and compound 4 {(17b-17-hydroxy-17-methyl androsta [1a, 2a] cyclohex (2’,5’ methylene 3’, 4-diene-3-one}, relative to compound 1. The results indicated that thedDiels-Alder reactionddid notpproceed under the usual circumstances of high pressure and temperature, but could proceed in the presence of a Lewis acid (AlCl3. The structures of compounds 3 and 4 were confirmed by spectroscopic methods. The androgenic behavior of compounds 3 and 4 in comparison to compound 1 in the apomorphine test indicated that both compounds were almost devoid of androgenic activity, but prevented apomorphine mediated penile erection in male rats in a similar manner as cyproterone acetate.

  3. Microstructure evolution and tribological properties of acrylonitrile-butadiene rubber surface modified by atmospheric plasma treatment

    Science.gov (United States)

    Shen, Ming-xue; Zhang, Zhao-xiang; Peng, Xu-dong; Lin, Xiu-zhou

    2017-09-01

    For the purpose of prolonging the service life for rubber sealing elements, the frictional behavior of acrylonitrile-butadiene rubber (NBR) surface by dielectric barrier discharge plasma treatments was investigated in this paper. Surface microstructure and chemical composition were measured by atomic force microscopy, field-emission scanning electron microscopy, and X-ray photoelectron spectroscopy, respectively. Water contact angles of the modified rubber surface were also measured to evaluate the correlation between surface wettability and tribological properties. The results show that plasma treatments can improve the properties of the NBR against friction and wear effectively, the surface microstructure and roughness of plasma-modified NBR surface had an important influence on the surface tribological behavior, and the wear depth first decreased and then increased along with the change of plasma treatment time. It was found that the wettability of the modified surface was gradually improved, which was mainly due to the change of the chemical composition after the treatment. This study suggests that the plasma treatment could effectively improve the tribological properties of the NBR surface, and also provides information for developing wear-resistant NBR for industrial applications.

  4. Styrene-butadiene rubber/halloysite nanotubes nanocomposites modified by sorbic acid

    Energy Technology Data Exchange (ETDEWEB)

    Guo Baochun, E-mail: psbcguo@scut.edu.cn [Department of Polymer Materials and Engineering, South China University of Technology, Guangzhou 510640 (China); Chen Feng; Lei Yanda; Liu Xiaoliang; Wan Jingjing; Jia Demin [Department of Polymer Materials and Engineering, South China University of Technology, Guangzhou 510640 (China)

    2009-05-30

    Sorbic acid (SA) was used to improve the performance of styrene-butadiene rubber (SBR)/halloysite nanotubes (HNTs) nanocomposites by direct blending. The detailed mechanisms for the largely improved performance were studied by X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), differential scanning calorimetry (DSC), porosity analysis and crosslink density determination. The strong interfacial bonding between HNTs and rubber matrix is resulted through SA intermediated linkages. SA bonds SBR and HNTs through grafting copolymerization/hydrogen bonding mechanism. Significantly improved dispersion of HNTs in virtue of the interactions between HNTs and SA was achieved. Formation of zinc disorbate (ZDS) was revealed during the vulcanization of the composites. However, in the present systems, the contribution of ZDS to the reinforcement was limited. Effects of SA content on the vulcanization behavior, morphology and mechanical properties of the nanocomposites were investigated. Promising mechanical properties of SA modified SBR/HNTs nanocomposites were obtained. The changes in vulcanization behavior, mechanical properties and morphology were correlated with the interactions between HNTs and SA and the largely improved dispersion of HNTs.

  5. Styrene-butadiene rubber/halloysite nanotubes nanocomposites modified by sorbic acid

    Science.gov (United States)

    Guo, Baochun; Chen, Feng; Lei, Yanda; Liu, Xiaoliang; Wan, Jingjing; Jia, Demin

    2009-05-01

    Sorbic acid (SA) was used to improve the performance of styrene-butadiene rubber (SBR)/halloysite nanotubes (HNTs) nanocomposites by direct blending. The detailed mechanisms for the largely improved performance were studied by X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), differential scanning calorimetry (DSC), porosity analysis and crosslink density determination. The strong interfacial bonding between HNTs and rubber matrix is resulted through SA intermediated linkages. SA bonds SBR and HNTs through grafting copolymerization/hydrogen bonding mechanism. Significantly improved dispersion of HNTs in virtue of the interactions between HNTs and SA was achieved. Formation of zinc disorbate (ZDS) was revealed during the vulcanization of the composites. However, in the present systems, the contribution of ZDS to the reinforcement was limited. Effects of SA content on the vulcanization behavior, morphology and mechanical properties of the nanocomposites were investigated. Promising mechanical properties of SA modified SBR/HNTs nanocomposites were obtained. The changes in vulcanization behavior, mechanical properties and morphology were correlated with the interactions between HNTs and SA and the largely improved dispersion of HNTs.

  6. 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.

  7. 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.

  8. 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.

  9. 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.

  10. Bond Characteristics of Macro Polypropylene Fiber in Cementitious Composites Containing Nanosilica and Styrene Butadiene Latex Polymer

    Directory of Open Access Journals (Sweden)

    Jae-Woong Han

    2015-01-01

    Full Text Available This study evaluated the bond properties of polypropylene (PP fiber in plain cementitious composites (PCCs and styrene butadiene latex polymer cementitious composites (LCCs at different nanosilica contents. The bond tests were evaluated according to JCI SF-8, in which the contents of nanosilica in the cement were 0, 2, 4, 6, 8, and 10 wt%, based on cement weight. The addition of nanosilica significantly affected the bond properties between macro PP fiber and cementitious composites. For PCCs, the addition of 0–2 wt% nanosilica enhanced bond strength and interface toughness, whereas the addition of 4 wt% or more reduced bond strength and interface toughness. The bond strength and interfacial toughness of LCCs also increased with the addition of up to 6% nanosilica. The analysis of the relative bond strength showed that the addition of nanosilica affects the bond properties of both PCC and LCC. This result was confirmed via microstructural analysis of the macro PP fiber surface after the bond tests, which revealed an increase in scratches due to frictional forces and fiber tearing.

  11. Methods for measurement of reactive metabolites as a basis for cancer risk assessment: Application to 1,3-butadiene and isoprene

    Energy Technology Data Exchange (ETDEWEB)

    Fred, Charlotta [Stockholm Univ. (Sweden). Dept. of Environmental Chemistry

    2005-02-01

    1,3-Butadiene is a general air pollutant associated with combustion of organic matter and is also an extensively used monomer in polymer production. The cancer risk estimation of 1,3-butadiene is encumbered with large uncertainties. Extrapolation from tumour frequencies in long-term animal tests has led to a relatively high figure for the risk associated with 1,3-butadiene exposure. This is mainly based on observations of very high tumour incidences in butadiene-exposed mice, which in this respect are about 100 times more sensitive than rats. It has been hypothesized that a high cancer risk from 1,3-butadiene could be associated with its metabolism to the bifunctional 1,2:3,4-diepoxybutane (DEB) which, in comparison with monofunctional epoxides, 1,2-epoxy-3-butene (EB) and 1,2-epoxy-3,4-butanediol (EBdiol), is a highly effective mutagen, i.e. cancer initiator. Measurement of in vivo doses of DEB is therefore essential for the risk assessment of 1,3-butadiene. Reaction products with hemoglobin offer a possibility of measuring reactive metabolites in vivo. Hemoglobin adducts from EBdiol have in this study been measured with available methods, which are, however, not applicable to the bifunctional DEB, and method development was therefore needed. This work presents a procedure for measurement of a specific, ring-closed adduct, Pyr-Val, formed from the reaction of DEB with N-terminal valines in hemoglobin. It is based on LC-ESI-MS/MS analysis of the Pyr-modified N-terminal peptides enriched after trypsin digestion of globin. Mouse and rat could be compared regarding the metabolism of EB, DEB and EBdiol. From the data it was concluded that, in 1,3-butadiene exposure, about 60 times higher levels of DEB are formed in mice compared to rats. Estimates of in vivo doses in published cancer tests showed that carcinogenesis in mice is mainly due to DEB, whereas in rat, and possibly man, the monofunctional EBdiol is the predominant causative factor. Preliminarily, the cancer

  12. 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.

  13. Synthesis of Ethylene or Propylene/1,3-Butadiene Copolymers Possessing Pendant Vinyl Groups with Virtually No Internal Olefins

    Directory of Open Access Journals (Sweden)

    Kenji Michiue

    2015-11-01

    Full Text Available In general, ethylene/1,3-butadiene copolymerizations provides copolymers possessing both pendant vinyls and vinylenes as olefinic moieties. We, at MCI, studied the substituent effects of C2-symmetric zirconocene complexes, rac-[Me2Si(Indenyl’2]ZrCl2 (Indenyl’ = generic substituted indenyl, after activation on the ratio of the pendant vinyls and vinylenes of the resultant copolymers. Complexes examined in this study were rac-dimethylsilylbis (1-indenylzirconium dichloride (1, rac-dimethylsilyl-bis[1-(2-methyl-4,5-benzoindenyl] zirconium dichloride (2, rac-dimethylsilyl-bis[l-(2-methyl -4-phenylindenyl]zirconium dichloride (3, rac-dimethy1si1y1- bis(2-ethyl-4-phenylindenyl zirconium dichloride (4, rac-dimethylsilyl-bis[l-(2-n-propyl -4-(1-naphthylindenyl]zirconium dichloride (5, rac-dimethylsilyl-[1-(2-ethyl-4-(5-(2,2-dimethyl-2,3-dihydro-1H-cyclopenta [a]naphthalenylindenyl][1-(2-n-propyl-4-(5-(2,2-dimethyl-2,3-dihydro-1H-cyclopenta[a] naphthalenylindenyl]zirconium dichloride (6, rac-dimethylsilyl-bis[1-(2-ethyl-4-(9-phenanthrylindenyl]zirconium dichloride (7, and rac-dimethylsilyl-bis[l-(2-n-propyl-4-(9-phenanthrylindenyl]zirconium dichloride (8. We found that the ratio of the pendant vinyls and vinylenes is strongly affected by the bulkiness of the substituent on the complexes examined. The vinyl content increased linearly in the following order, 8 > 7 > 6 > 5 > 4 > 3 > 2 > 1. Notably, complex 8/DMAO formed ethylene/1,3-butadiene copolymers possessing predominant vinyl groups, which can be crucial precursors for functionalized polyolefins. Likewise, complex 8/DMAO afforded propylene/1,3-butadiene copolymers with predominant vinyl groups.

  14. Products of the gas-phase reactions of 1,3-butadiene with OH and NO{sub 3} radicals

    Energy Technology Data Exchange (ETDEWEB)

    Tuazon, E.C.; Alvarado, A.; Aschmann, S.M.; Atkinson, R.; Arey, J.

    1999-10-15

    1,3-Butadiene is emitted into the atmosphere from a number of sources including combustion sources and is listed in the US as a hazardous air pollutant. In the atmosphere, 1,3-butadiene reacts with OH radicals, NO{sub 3} radicals, and O{sub 3} with the dominant tropospheric removal processes being daytime reaction with the OH radical and nighttime reaction with the NO{sub 3} radical. The authors have used gas chromatography, in situ Fourier transform infrared (FT-IR) absorption spectroscopy, and in situ atmospheric pressure ionization tandem mass spectrometry (API-MS) to identify and quantify the products formed from the reactions of 1,3-butadiene with OH radicals (in the presence of NO) and NO{sub 3} radicals. Acrolein, formaldehyde, and furan were identified and quantified from the OH radical-initiated reaction, with formation yields of 0.58 {+-} 0.04, 0.62 {+-} 0.05, and 0.03--0.04, respectively. Organic nitrates were observed by FT-IR spectroscopy with an estimated yield of 0.07 {+-} 0.03, and the API-MS analyses indicated that these organic nitrates are mainly the hydroxynitrate HOCH{sub 2}CH=CHCH{sub 2}ONO{sub 2} and/or its isomers. API-MS analyses showed the formation of a hydroxycarbonyl with the formula C{sub 4}H{sub 6}O{sub 2}, attributed to HOCH{sub 2}CH=CHCHO and/or its isomers. The major products of the NO{sub 3} radical-initiated reaction were organic nitrates; the API-MS analyses indicated the formation of acrolein, 1,2-epoxy-3-butene, and unsaturated C{sub 4}-hydroxycarbonyls, hydroxynitrates, carbonyl nitrates, and nitrooxyhydroperoxides. Acrolein, HCHO, and furan were again quantified by gas chromatographic and FT-IR analyses. The data is compared with previous literature studies, and detailed reaction mechanisms are presented and discussed.

  15. C,C Couplings in the Reactions of Unsaturated Group 4 Metal s-cis-Butadiene Complexes with 2,6-Xylyl Isocyanide

    OpenAIRE

    Hessen, Bart; Blenkers, Joop; Teuben, Jan H.; Helgesson, Göran; Jagner, Susan

    1989-01-01

    A group of electronically unsaturated (14-electron) diene complexes of Hf and Ti has been reacted with 2,6-xylyl isocyanide. Cp*Hf(diene)Cl (diene = 2,3-dimethyl-1,3-butadiene, 2-methyl-1,3-butadiene; Cp* = η-C5Me5) reacts with 2 mol of isocyanide to form the unusual heterospiro complexes Cp*Hf(Cl)N(xy)CCH2C(Me)=C(R)CH=CHN(xy) (R = H, Me; xy = 2,6-xylyl) involving a 1,2-hydrogen shift and a ring closure after insertion of isocyanide into the Hf-diene bond. In Cp*Hf(2,3-dimethyl-1,3-butadiene)...

  16. Preparation, characterization and conductivity study of nitro-mercurated styrene butadiene rubber/silver doped zinc oxide nanocomposites

    Science.gov (United States)

    Anilkumar, T.; Naik, Adarsh Ajith; Ramesan, M. T.

    2017-06-01

    Here we report the preparation of nitromercurated styrene butadiene rubber (NMSBR)/silver doped zinc oxide nanocomposite by inexpensive and ecofriendly two roll mill mixing. The composites were characterized by UV, FTIR, XRD, SEM, TGA and conductivity measurements. UV and FTIR spectrum indicated the interfacial interaction between the polymer and nanoparticles.XRD and SEM images showed the uniform arrangement of nanoparticles within the macromolecular chain. TGA study indicated the better thermal resistance of the composite. The dielectric properties and AC conductivity ofnanocomposites were much greater than nitromercurated SBR and they may be used as multifunctional materials for nanoelectronic devices.

  17. Effect of crosslinking density on biaxial relaxation of SBR by using reduced variables. [Styrene-Butadiene Rubber

    Science.gov (United States)

    Arenz, R. J.

    1974-01-01

    The use of reduced variables to account for the effect of crosslinking density in a styrene-butadiene rubber (SBR) system is demonstrated for general biaxial stress states. Recently published results from stress relaxation tests on five SBR vulcanizates crosslinked to different degrees by tetramethylthiuram disulfide were superposed by using the crosslinking density as a reduction variable. The equilibrium shear modulus calculated from the master relaxation curve at long reduced times was in satisfactory agreement with other results for SBR. The time-axis shifts were related in a linear logarithmic manner to the crosslinking density but had a slope slightly less than values previously reported for elastomer systems.

  18. Study of the mechanical properties of Acrylonitrile Butadiene Styrene - High Impact Polystyrene blends with Styrene Ethylene Butylene Styrene

    OpenAIRE

    PEYDRO Miguel Angel; JUAREZ David; Sanchez-Caballero, Samuel; PARRES Francisco

    2013-01-01

    A binary blend Acrylonitrile Butadiene Styrene ¿ High Impact Polystyrene (ABS-HIPS 50% wt) was prepared on a twin-screw extruder at 190-210 oC. The different mechanical properties were then analyzed using tensile strength and impact tests. The analysis of mechanical properties showed a decrease in elongation at break and impact strength. On the other hand, we have prepared ternary blends of ABS-HIPS- Styrene Ethylene Butylene Styrene (SEBS), varying the percentage of SEBS from 10 to 30 %wt us...

  19. Measurement of acrolein and 1,3-butadiene in a single puff of cigarette smoke using lead-salt tunable diode laser infrared spectroscopy

    Science.gov (United States)

    Thweatt, W. Dave; Harward, Charles N., Sr.; Parrish, Milton E.

    2007-05-01

    Acrolein and 1,3-butadiene in cigarette smoke generally are measured using two separate analytical methods, a carbonyl derivative HPLC method for acrolein and a volatile organic compound (VOC) GC/MS method for 1,3-butadiene. However, a single analytical method having improved sensitivity and real-time per puff measurement will offer more specific information for evaluating experimental carbon filtered cigarettes designed to reduce the smoke deliveries of these constituents. This paper describes an infrared technique using two lead-salt tunable diode lasers (TDLs) operating with liquid nitrogen cooling with emissions at 958.8 cm -1 and 891.0 cm -1 respectively for the simultaneous measurement of acrolein and 1,3-butadiene, respectively, in each puff of mainstream cigarette smoke in real time. The dual TDL system uses a 3.1 l volume, 100 m astigmatic multiple pass absorption gas cell. Quantitation is based on a spectral fit that uses previously determined infrared molecular line parameters generated in our laboratory, including line positions, line strengths and nitrogen-broadened half-widths for these species. Since acrolein and ethylene absorption lines overlap and 1,3-butadiene, ethylene and propylene absorption lines overlap, the per puff deliveries of ethylene and propylene were determined since their overlapping absorption lines must be taken into account by the spectral fit. The acrolein and 1,3-butadiene total cigarette deliveries for the 1R5F Kentucky Reference cigarette were in agreement with the HPLC and GC/MS methods, respectively. The limit of detection (LOD) for 1,3-butadiene and acrolein was 4 ng/puff and 24 ng/puff, respectively, which is more than adequate to determine at which puff they break through the carbon filter. The retention and breakthrough behavior for the two primary smoke constituents depend on the cigarette design and characteristics of the carbon filter being evaluated.

  20. Chemo-, regio-, and stereoselective cyclizations of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with alpha-chloroacetic acid chlorides and alpha-chloroacetic acetals.

    Science.gov (United States)

    Langer, P; Krummel, T

    2001-04-17

    Treatment of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with alpha-chlorocarboxylic acid chlorides resulted in chemo- and regioselective formation of 6-chloro3,5-dioxo esters, which were regioselectively converted into functionalised 3(2H)furanones. Chemo- and regioselective condensation of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with alpha-chloroacetic dimethyl acetal afforded 6-chloro-5-methoxy-3-oxo esters, which could be regio- and stereoselectively transformed into 2-alkylidene-4-methoxytetrahydrofurans.

  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. Analysis of recycled poly (styrene-co-butadiene) sulfonation: a new approach in solid catalysts for biodiesel production.

    Science.gov (United States)

    Aguilar-Garnica, Efrén; Paredes-Casillas, Mario; Herrera-Larrasilla, Tito E; Rodríguez-Palomera, Felicia; Ramírez-Arreola, Daniel E

    2013-01-01

    The disposal of solid waste is a serious problem worldwide that is made worse in developing countries due to inadequate planning and unsustainable solid waste management. In Mexico, only 2% of total urban solid waste is recycled. One non-recyclable material is poly (styrene-co-butadiene), which is commonly used in consumer products (like components of appliances and toys), in the automotive industry (in instrument panels) and in food services (e.g. hot and cold drinking cups and glasses). In this paper, a lab-scale strategy is proposed for recycling poly (styrene-co-butadiene) waste by sulfonation with fuming sulfuric acid. Tests of the sulfonation strategy were carried out at various reaction conditions. The results show that 75°C and 2.5 h are the operating conditions that maximize the sulfonation level expressed as number of acid sites. The modified resin is tested as a heterogeneous catalyst in the first step (known as esterification) of biodiesel production from a mixture containing tallow fat and canola oil with 59% of free fatty acids. The preliminary results show that esterification can reach 91% conversion in the presence of the sulfonated polymeric catalyst compared with 67% conversion when the reaction is performed without catalyst.

  3. Inhalation toxicity studies with 1,3-butadiene 3 two year toxicity/carcinogenicity study in rats

    Energy Technology Data Exchange (ETDEWEB)

    Owen, P.E.; Glaister, J.R.; Gaunt, I.F.; Pullinger, D.H.

    1987-05-01

    Groups of 110 male and 110 female CD (Sprague-Dawley) rats were exposed to atmospheres containing 0 (control), 1000 or 8000 ppm v/v butadiene for 6 hr/day and 5 days/week. Ten of each sex from each group were killed at 52 weeks. The study was terminated when it was predicted that survival would drop to 20% to 25%. High dose rats had wet, ruffled fur and showed slight incoordination during the first exposure each week. During the second year, mortality in both treated female groups was increased because of humanitarian sacrifice of animals with large subcutaneous masses, while increased mortality in the high dose males was accompanied by an increase of the severity of nephropathy. Body weight was slightly lower than controls in both sexes at the high dose, but statistically significant only over the first 12 weeks. There were no effects in hematological analyses or tests of neuromuscular function that definitely could be associated with treatment. Liver weights at both doses were increased in both sexes with no associated pathological change. Kidney weight was increased in males at the high dose, together with an increase in the severity of nephrosis. There were increases in the incidences of pancreatic exocrine adenoma; uterine sarcoma; Zymbal gland carcinoma; mammary tumors; thyroid follicular cell tumors; and testis Leydig-cell tumors. These data suggest the butadiene is a weak oncogen to the rat under the conditions of exposure used in this study.

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

    Science.gov (United States)

    Desrousseaux, Camille; Cueff, Régis; Aumeran, Claire; Garrait, Ghislain; Mailhot-Jensen, Bénédicte; Traoré, Ousmane; Sautou, Valérie

    2015-01-01

    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.

  5. Inner Stucture of Thin Films of Lamellar Poly(styrene-b-butadiene) Diblock Copolymers as revealed by Grazing-Incidence Small-Angle Scattering

    DEFF Research Database (Denmark)

    Busch, Peter; Posselt, Dorthe; Smilgies, Detlef-Matthias

    2007-01-01

    The lamellar orientation in supported, thin films of poly(styrene-b-butadiene) (P(S-b-B)) depends on block copolymer molar mass. We have studied films from nine block copolymer samples with molar masses between 13.9 and 183 kg/mol using grazing-incidence small-angle X-ray scattering (GISAXS) and ...

  6. Pd/TOMPP-catalysed telomerisation of 1,3-butadiene with lignin-type phenols and thermal Claisen rearrangement of linear telomers

    NARCIS (Netherlands)

    Hausoul, P.J.C.; Tefera, S.D.; Blekxtoon, J.; Bruijnincx, P.C.A.; Klein Gebbink, R.J.M.; Weckhuysen, B.M.

    2013-01-01

    The Pd/TOMPP-catalysed (TOMPP = tris(2-methoxyphenyl)phosphine) telomerisation of 1,3-butadiene was studied under solvent- and base-free conditions with phenolic substrates that can be potentially derived from lignin. Large differences in catalytic activity were observed, with reactivity increasing

  7. Pathway and Surface Mechanism Studies of 1,3-butadiene Selective Oxidation Over Vanadium-Molybdenum-Oxygen Catalysts

    Energy Technology Data Exchange (ETDEWEB)

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

    2001-01-01

    The partial oxidation of 1,3-butadiene has been investigated over VMoO catalysts synthesized by sol-gel techniques. Surface areas were 9-14 m2/g, and compositions were within the solid solution regime, i.e. below 15.0 mol % MoO3/(MoO3 + V2O5). Laser Raman Spectroscopy and XRD data indicated that solid solutions were formed, and pre- and post-reaction XPS data indicated that catalyst surfaces contained some V+4 and were further reduced in 1,3-butadiene oxidation. A reaction pathway for 1,3-butadiene partial oxidation to maleic anhydride was shown to involve intermediates such as 3,4-epoxy-1-butene, crotonaldehyde, furan, and 2-butene-1,4-dial. The addition of water to the reaction stream substantially increased catalyst activity and improved selectivity to crotonaldehyde and furan at specific reaction temperatures. At higher water addition concentrations, furan selectivity increased from 12% to over 25%. The catalytic effects of water addition were related to competitive adsorption with various V2O5-based surface sites, including the vanadyl V=O, corner sharing V-O-V and edge sharing V-O oxygen. Higher levels of water addition were proposed to impose acidic character by dissociative adsorption. In addition, a novel combinatorial synthesis technique for VMoO was used to investigate the phase transitions of V2O5, solid solutions of Mo in V2O5, V9Mo6O40, and other reduced VMoO compounds, characterized by laser Raman spectroscopy. The natural composition gradient imposed by the sputter deposition apparatus was used to create VMoO arrays containing 225 samples ranging from 7.0-42 mol% MoO3/(V2O5 + MoO3), determined by EDS analysis.

  8. Effect of Zinc Oxide Modified Silica Particles on the Molecular Dynamics of Carboxylated Acrylonitrile-Butadiene Rubber Composites

    Directory of Open Access Journals (Sweden)

    Magdalena Gaca

    2017-11-01

    Full Text Available This work examines the molecular dynamics of carboxylated acrylonitrile-butadiene rubber crosslinked with zinc oxide modified silica particles. ZnO/SiO2 with the wide range of ZnO concentrations were used as both a crosslinking agent and filler. A series of thermal measurements were applied to the characterization of the samples: differential scanning calorimetry, dynamical mechanical thermal analysis, and dielectric relaxation spectroscopy. A complementary experimental technique, which is equilibrium swelling in solvents, confirms the presence of ionic crosslinks, which are created between zinc ions and the functional carboxyl groups of the rubber, within the structure of the vulcanizates. These interactions influenced not only the affinity of the vulcanizates to solvents, but also their dynamic mechanical and dielectric properties. In these investigations, the influence of concentration of ZnO on the surface of the ZnO/SiO2 on the properties of the vulcanizates are described.

  9. Hardness and swelling behaviour of epoxidized natural rubber/recycled acrylonitrile-butadiene rubber (ENR 50/NBRr) blends

    Science.gov (United States)

    Ahmad, Hazwani Syaza; Ismail, Hanafi; Rashid, Azura A.

    2017-07-01

    This recent work is to investigate the hardness and swelling behaviour of epoxidized natural rubber/recycled acrylonitrile-butadiene rubber (ENR 50/NBRr) blends. ENR 50/NBRr blends were prepared by two-roll mills with five different loading of NBRr from 5 to 35 phr. Results indicated that the hardness of ENR 50/NBRr blends increased as recycled NBR increased due to the improvement in crosslink density of the blends. Increasing NBRr content gives ENR 50/NBRr blends better resistance towards swelling. Higher degree of crosslinking will increase the swelling resistance and reduce the penetration of toluene into the blends. The presence of polar group in ENR 50 and NBRr give better hardness properties and swelling behaviour of the ENR 50/NBRr blends compared to the NR/NBRr blends.

  10. Studies on gel electrolyte based on nitrile-butadiene copolymers. Final report, 1 November 1991-30 November 1992

    Energy Technology Data Exchange (ETDEWEB)

    Sircar, A.K.; Kumar, B.; Linden, S.M.; Weissman, P.T.

    1993-06-01

    This study is concerned with the preparation of a hybrid electrolyte, suitable for solid-polymer batteries. Based on the study of ionic conductivity in the presence of LiBF4 of a number of nitrile-butadiene copolymers (NBR), hydrogenated NBR (HNBR) was selected as the host polymer. DC conductivity studies with three different lithium salts in different plasticizers showed the highest conductivity for LiBF4. Conductivity of LiBF4 in different plasticizers decreases in the order DMF > DMAC > Gamma butyrolactone > NMP > PC=gamma-valerolactone > glymes. NMP was chosen as the plasticizer for hybrid films based on its moderate conductivity, low vapor pressure, and low freezing point. Polymer electrolytes, Gel electrolytes, Ionic conductivity.

  11. A styrene-butadiene rubber (SBR)/carbon nanotube-based smart force sensor for automotive tire deformation monitoring

    Science.gov (United States)

    Cho, Min-Young; Kim, Ji-Sik; Lee, Ho-Geun; Choi, Seung-Bok; Kim, Gi-Woo

    2016-04-01

    This paper provides a preliminary study on the piezoresistive effect of a styrene-butadiene Rubber (SBR), one of the main ingredients of automotive tire, dispersed with carbon nanotubes (CNTs) to explore its feasibility as a force sensor embedded in automotive tires. Typically, the application of CNTs has been successfully applied to the mechanical sensing technology such as a stress/strain and impact sensor. In this study, the potential of using the SBR/CNT as a force sensor for monitoring automotive tire deformation is evaluated for the first time. Experimental results show that the electrical resistance of the SBR/CNT composite changes in response to the sinusoidal loading, as well as static compressive load. These piezoresistive responses of the SBR/CNT composite will be used for sensing the tire deformation caused by the vehicle loading or cracks of tires.

  12. Prediction of Flexural Strength of Concretes Containing Silica Fume and Styrene-Butadiene Rubber (SBR) with an Empirical Model

    Science.gov (United States)

    Shafieyzadeh, M.

    2015-12-01

    In the flexural test, the theoretical maximum tensile stress at the bottom fiber of a test beam is known as the modulus of rupture or flexural strength. This work deals with the effects of Silica Fume and Styrene-Butadiene Latex (SBR) on flexural strength of concrete. An extensive experimentation was carried out to determine the effects of silica fume and SBR on flexural strength of concrete. Two water-binder ratios and several percentages of silica fume and SBR were considered. Abrams' Law, which was originally formulated for conventional concrete containing cement as the only cementations material, is used for prediction of flexural strength of these concretes. The aim of this work is to construct an empirical model to predict the flexural strength of silica fume-SBR concretes using concrete ingredients and time of curing in water. Also, the obtained results for flexural strength tests have been compared with predicted results.

  13. Organic Semiconducting Materials in Film and Powder Forms from a Co-polymeric Elastomer-Styrene Butadiene Rubber

    Science.gov (United States)

    Santhamma, G.; Predeep, P.

    2008-04-01

    Semiconducting materials in both film and powder forms are prepared by Antimony Pentachloride (SBCl5) doping in Styrene Butadiene Rubber (SBR). SBR is a synthetic co-polymeric elastomer, insulating in undoped state, is mainly used for manufacturing tires, tubes etc. Synthesized conducting materials are proposed to have tremendous application potentials in optoelectronic, electronic and electrical industries. For example conducting films can be used as active elements for fabrication of organic light emitting diodes, photovoltaic cells etc. Electrical and optical properties of prepared samples are studied by measuring electrical conductivity and analyzing spectroscopic data. Electrical conductivity of samples lies in the range of that of semi-conducting materials. Presence of conjugated sequences in the back bone of prepared conducting materials, which is regarded as pre-requisite condition for a polymer to conductive, is confirmed by studying UV/Vis spectra.

  14. [Determination of lead, cadmium, mercury, chromium and arsenic in acrylonitrile-butadiene-styrene copolymer using microwave digestion-ICP-MS].

    Science.gov (United States)

    Wang, Ying-Feng; Shi, Yan-Zhi; Zhang, Hua; Chen, Yu-Hong; Lau, John; Wilbur, Steven; Li, Ping

    2008-01-01

    A method was studied for the analysis of Cr, As, Cd, Hg and Pb in acrylonitrile-butadiene-styrene copolymer by using ICP-MS. The instrument parameters were optimized and the introduction system was developed systematically. The sample is decomposed by microwave digestion. The digestion condition was optimized concerning digestion system, proportion of acids and digestion procedure, which affords reference for the preparation of the same kinds of polymer samples. The detection limits of the method for all sample elements were 0.7-6.5 ng x g(-1), the recoveries were 89.8%-110.8%, and the RSDs were 2.8%-11.3%. The analytical method presented was characterized with good precision and accuracy, simplicity, rapidness, low limits of detection and no matrix matching requirements.

  15. Modification of asphaltic concrete with a mineral polymeric additive based on butadiene-styrene rubber and chemically precipitated calcium carbonate

    Directory of Open Access Journals (Sweden)

    S. I. Niftaliev

    2016-01-01

    Full Text Available Modification of asphaltic concrete with a mineral polymeric additive based on butadiene – styrene rubber and chemically precipitated calcium carbonate. This paper presents the results of the study of physical – mechanical and service properties of the asphaltic concrete modified with the mineral polymeric composition. Calcium carbonate is used both as a filler and a coagulant. The chalk was preliminarily ground and hydrophobizated by stearic acid. These operations contribute to even distribution of the filler and interfere with lump coagulation. As a result of the experiments, it was found that the best results were obtained by combining the operations of dispersion and hydrophobization. The optimal amount of stearic acid providing the finest grinding in a ball mill is a content from 3 to 5% by weight. The optimal grinding time of the filler was found (4–6 hours. With increasing dispersion time the particles form agglomerates. Filling the butadiene styrene latex with the hydrophobic fine-grained calcium carbonate was carried out in the laboratory mixer. As a result of the experimental works, it was found that the best distribution of the filler takes place with ratio of rubber: chalk – 100:400. The resulting modifier was subjected to the thermal analysis on the derivatograph to determine its application temperature interval. A marked reduction in weight of the mineral polymeric modifier begins at 350 °C. Thus, high temperature of the modifier destruction allows to use it at the temperature of the technological process of asphaltic concrete preparation (up to 170 °C. It was found that an increase in the amount of the carbonate filler in the rubber SKS 30АRК significantly increases its thermal resistance and connection of the polymer with the chalk in the composition.

  16. 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

  17. Plastics piping systems for industrial applications : acrylonitrile-butadiene- styrene (ABS), unplasticized poly(vinyl chloride) (PVC-U) and chlorinated poly(vinyl chloride) (PVC-C) : specifications for components and the system : metric series

    CERN Document Server

    International Organization for Standardization. Geneva

    2003-01-01

    Plastics piping systems for industrial applications : acrylonitrile-butadiene- styrene (ABS), unplasticized poly(vinyl chloride) (PVC-U) and chlorinated poly(vinyl chloride) (PVC-C) : specifications for components and the system : metric series

  18. Radiation preparation of nano-powdered styrene-butadiene rubber (SBR) and its toughening effect for polystyrene and high-impact polystyrene

    Energy Technology Data Exchange (ETDEWEB)

    Li Daishuang; Xia Haibing [Department of Applied Chemistry, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China); Peng Jing [Department of Applied Chemistry, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China)], E-mail: jpeng@pku.edu.cn; Zhai Maolin; Wei Genshuan; Li Jiuqiang [Department of Applied Chemistry, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China); Qiao Jinliang [Department of Applied Chemistry, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China); SINOPEC, Beijing Research Institute of Chemical Industry, Beijing 100013 (China)

    2007-11-15

    Nano-powdered styrene-butadiene rubber (NPSBR) was synthesized based on the styrene-butadiene rubber (SBR) latex via gamma radiation crosslinking followed by spray drying. Two functional monomers, 2-ethyl hexyl acrylate (2-EHA) and trimethylolpropane triacrylate (TMPTA) were used as crosslinking agents. It was found that both 2-EHA and TMPTA can improve the radiation crosslinking of SBR latex. Transmission electron microscope (TEM) and scanning electron microscope (SEM) revealed that the NPSBR has a particle size similar to that of SBR latex with a diameter of 100 nm due to the high degree of crosslinking of SBR. Mechanical testing results showed that NPSBR could toughen polystyrene (PS) and high-impact polystyrene (HIPS) effectively. In addition, NPSBR is more suitable to toughen HIPS than PS at low rubber content.

  19. The Diels-Alder Cycloaddition Reaction of Substituted Hemifullerenes with 1,3-Butadiene: Effect of Electron-Donating and Electron-Withdrawing Substituents.

    Science.gov (United States)

    Mojica, Martha; Méndez, Francisco; Alonso, Julio A

    2016-02-12

    The Diels-Alder (DA) reaction provides an attractive route to increase the number of six member rings in substituted Polycyclic Aromatic Hydrocarbons (PAHs). The density functional theory (DFT) B3LYP method has been used in this work to inquire if the substitution of H over the edge of triindenetriphenylene (pristine hemifullerene 1) and pentacyclopentacorannulene (pristine hemifullerene 2), could improve the DA cycloaddition reaction with 1,3-butadiene. The substituents tested include electron-donating (NH₂, OMe, OH, Me, i-Pr) and electron-withdrawing groups (F, COOH, CF₃, CHO, CN, NO₂). The electronic, kinetic and thermodynamic parameters of the DA reactions of the substituted hemifullerenes with 1,3-butadiene have been analyzed. The most promising results were obtained for the NO₂ substituent; the activation energy barriers for reactions using this substituent were lower than the barriers for the pristine hemifullerenes. This leads us to expect that the cycloadditions to a starting fullerene fragment will be possible.

  20. Synthesis of oxa-bridged derivatives from Diels–Alder bis-adducts of butadiene and 1,2,3,4-tetrahalo-5,5-dimethoxycyclopentadiene

    Directory of Open Access Journals (Sweden)

    Faiz Ahmed Khan

    2010-06-01

    Full Text Available Bis-adducts of 1,2,3,4-tetrahalo-5,5-dimethoxycyclopentadiene and 1,3-butadiene, generated in situ from 3-sulfolene, have been synthesized in excellent yield. Ruthenium catalyzed oxidation of the bis-adducts followed by a one-pot transformation of the resulting α-diketone furnished oxa-bridged compounds. Unambiguous stereochemical assignments of both diastereomeric series are reported.

  1. Thio-Pybox and Thio-Phebox complexes of chromium, iron, cobalt and nickel and their application in ethylene and butadiene polymerisation catalysis.

    Science.gov (United States)

    Nobbs, James D; Tomov, Atanas K; Cariou, Renan; Gibson, Vernon C; White, Andrew J P; Britovsek, George J P

    2012-05-21

    A series of bis(thiazolinyl)- and bis(thiazolyl)pyridine Thio-Pybox ligands and their metal complexes of chromium(III), iron(II), cobalt(II) and nickel(II) has been prepared, as well as a nickel(II) complex containing a monoanionic bis(thiazolinyl)phenyl Thio-Phebox ligand. These new metal complexes have been characterised and used as catalysts, in combination with the co-catalyst MAO, for the polymerisation of ethylene and for the polymerisation of butadiene. In the case of ethylene polymerisation, the Thio-Pybox and Thio-Phebox metal complexes have shown relatively low polymerisation activities, much lower compared to the related bis(imino)pyridine complexes of the same metals. In the polymerisation of butadiene, several Thio-Pybox cobalt(II) complexes show very high activities, significantly higher than the other metal complexes with the same ligand. It is the metal, rather than the ligand, that appears to have the most profound effect on the catalytic activity in butadiene polymerisation, unlike in the polymerisation of ethylene, where bis(imino)pyridine ligands provide highly active catalysts for a range of 1st row transition metals.

  2. Rheological properties of styrene-butadiene rubber filled with electron beam modified surface treated dual phase fillers[Styrene-butadiene rubber (SBR); Electron beam; Filler; Rheology; Die swell; Activation energy

    Energy Technology Data Exchange (ETDEWEB)

    Shanmugharaj, A.M.; Bhowmick, A.K. E-mail: anilkb@rtc.iitkgp.ernet.in

    2004-01-01

    The rheological properties of styrene-butadiene rubber (SBR) loaded with dual phase filler were measured using Monsanto Processability Tester (MPT) at three different temperatures (100 deg. C, 110 deg. C and 130 deg. C) and four different shear rates (61.3, 306.3, 613, and 1004.5 s{sup -1}). The effect of electron beam modification of dual phase filler in absence and presence of trimethylol propane triacrylate (TMPTA) or triethoxysilylpropyltetrasulphide (Si-69) on melt flow properties of SBR was also studied. The viscosity of all the systems decreases with shear rate indicating their pseudoplastic or shear thinning nature. The higher shear viscosity for the SBR loaded with the electron beam modified filler is explained in terms of variation in structure of the filler upon electron beam irradiation. Die swell of the modified filler loaded SBR is slightly higher than that of the unmodified filler loaded rubber, which is explained by calculating normal stress difference for the systems. Activation energy of the modified filler loaded SBR systems is also slightly higher than that of the control filler loaded SBR system.

  3. Crossed beam reactions of the phenyl (C6H5; X(2)A1) and phenyl-d5 radical (C6D5; X(2)A1) with 1,2-butadiene (H2CCCHCH3; X(1)A').

    Science.gov (United States)

    Yang, Tao; Parker, Dorian S N; Dangi, Beni B; Kaiser, Ralf I; Kislov, Vadim V; Mebel, Alexander M

    2014-06-26

    We explored the reactions on the phenyl (C6H5; X(2)A1) and phenyl-d5 (C6D5; X(2)A1) radical with 1,2-butadiene (C4H6; X(1)A') at a collision energy of about 52 ± 3 kJ mol(-1) in a crossed molecular beam apparatus. The reaction of phenyl with 1,2-butadiene is initiated by adding the phenyl radical with its radical center to the π electron density at the C1/C3 carbon atom of 1,2-butadiene. Later, the initial collision complexes isomerize via phenyl group migration from the C1/C3 carbon atoms to the C2 carbon atom of the allene moiety of 1,2-butadiene. The resulting intermediate undergoes unimolecular decomposition through hydrogen atom emission from the methyl group of the 1,2-butadiene moiety via a rather loose exit transition state leading to 2-phenyl-1,3-butadiene in an overall exoergic reaction (ΔRG = -72 ± 10 kJ mol(-1)). This finding reveals the strong collision-energy dependence of this system when the data are compared with those of the phenyl radical with 1,2-butadiene previously recorded at collision energies up to 160 kJ mol(-1), with the previous study exhibiting the thermodynamically less stable 1-phenyl-3-methylallene (ΔRG = -33 ± 10 kJ mol(-1)) and 1-phenyl-2-butyne (ΔRG = -24 ± 10 kJ mol(-1)) to be the dominant products.

  4. The filler-rubber interface in styrene butadiene nanocomposites with anisotropic silica particles: morphology and dynamic properties.

    Science.gov (United States)

    Tadiello, L; D'Arienzo, M; Di Credico, B; Hanel, T; Matejka, L; Mauri, M; Morazzoni, F; Simonutti, R; Spirkova, M; Scotti, R

    2015-05-28

    Silica-styrene butadiene rubber (SBR) nanocomposites were prepared by using shape-controlled spherical and rod-like silica nanoparticles (NPs) with different aspect ratios (AR = 1-5), obtained by a sol-gel route assisted by a structure directing agent. The nanocomposites were used as models to study the influence of the particle shape on the formation of nanoscale immobilized rubber at the silica-rubber interface and its effect on the dynamic-mechanical behavior. TEM and AFM tapping mode analyses of nanocomposites demonstrated that the silica particles are surrounded by a rubber layer immobilized at the particle surface. The spherical filler showed small contact zones between neighboring particles in contact with thin rubber layers, while anisotropic particles (AR > 2) formed domains of rods preferentially aligned along the main axis. A detailed analysis of the polymer chain mobility by different time domain nuclear magnetic resonance (TD-NMR) techniques evidenced a population of rigid rubber chains surrounding particles, whose amount increases with the particle anisotropy, even in the absence of significant differences in terms of chemical crosslinking. Dynamic measurements demonstrate that rod-like particles induce stronger reinforcement of rubber, increasing with the AR. This was related to the self-alignment of the anisotropic silica particles in domains able to immobilize rubber.

  5. Hybrid joining of polyamide and hydrogenated acrylonitrile butadiene rubber through heat-resistant functional layer of silane coupling agent

    Science.gov (United States)

    Sang, Jing; Sato, Riku; Aisawa, Sumio; Hirahara, Hidetoshi; Mori, Kunio

    2017-08-01

    A simple, direct adhesion method was developed to join polyamide (PA6) to hydrogenated acrylonitrile butadiene rubber (HNBR) by grafting a functional layer of a silane coupling agent on plasma functionalized PA6 surfaces. The functional layer of the silane coupling agent was prepared using a self-assembly method, which greatly improved the heat resistance of PA6 from 153 °C up to 325 °C and the resulting PA6/HNBR joints showed excellent adhesion properties with cohesive failure between PA6 and HNBR. X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), and nanoscale infrared microscopy and chemical imaging (Nano-IR, AFM-IR) were employed to characterize the surfaces and interfaces. The Nano-IR analysis method was employed for the first time to analyze the chemical structures of the adhesion interfaces between different materials and to establish the interface formation mechanism. This study is of significant value for interface research and the study of adhesion between resins and rubbers. There is a promising future for heat-resistant functional layers on resin surfaces, with potential application in fuel hose composite materials for the automotive and aeronautical industries.

  6. Thermomechanical properties of zirconium tungstate/hydrogenated nitrile butadiene rubber (HNBR) composites for low-temperature applications

    Science.gov (United States)

    Akulichev, Anton G.; Alcock, Ben; Tiwari, Avinash; Echtermeyer, Andreas T.

    2016-12-01

    Rubber compounds for pressure sealing application typically have inferior dimensional stability with temperature fluctuations compared with their steel counterparts. This effect may result in seal leakage failures when subjected to decreases in temperature. Composites of hydrogenated nitrile butadiene rubber (HNBR) and zirconium tungstate as a negative thermal expansion filler were prepared in order to control the thermal expansivity of the material. The amount of zirconium tungstate (ZrW2O8) was varied in the range of 0 to about 40 vol%. The coefficient of thermal expansion (CTE), bulk modulus, uniaxial extension and compression set properties were measured. The CTE of the ZrW2O8-filled HNBR decreases with the filler content and it is reduced by a factor of 2 at the highest filler concentration used. The filler effect on CTE is found to be stronger when HNBR is below the glass transition temperature. The experimental thermal expansion data of the composites are compared with the theoretical estimates and predictions given by FEA. The effect of ZrW2O8 on the mechanical characteristics and compression set of these materials is also discussed.

  7. Stepwise swelling of a thin film of lamellae-forming poly(styrene-b- butadiene) in cyclohexane vapor

    KAUST Repository

    Di, Zhenyu

    2012-06-26

    We investigated the swelling of a thin film of lamellae-forming poly(styrene-b-butadiene) in cyclohexane vapor. The vapor pressure and thus the degree of swelling of the film are increased in a stepwise manner using a custom-built sample cell. The resulting structural changes during and after each step were followed in situ using time-resolved grazing-incidence small-angle X-ray scattering (GISAXS). During the first step, the lamellar thickness increases strongly, before it decreases again. At the same time, the full width at half-maximum (FWHM) of the diffuse Bragg reflection along the film normal has a sharp maximum. These observations point to the formation of new lamellae. During the subsequent swelling steps, the lamellar thickness overshoots only weakly. The behavior thus resembles qualitatively our previous results on a similar thin film during swelling in saturated vapor of cyclohexane; however, it deviates from earlier theoretical predictions. We propose a theory that is quantitatively correct for the description of the dependence of the lamellar thickness on the polymer volume fraction in the late stage of the swelling steps. © 2012 American Chemical Society.

  8. Trans-1,4 selective polymerization of 1,3-butadiene with symmetry pincer chromium complexes activated by MMAO

    KAUST Repository

    Gong, Dirong

    2014-09-01

    Tridentate chromium complexes (Cr1-Cr7) incorporated with symmetrical pincer ligand bis(arylimino)pyridine and bis(pyrzaolyl)pyridine have been synthesized and characterized by elemental analyis, FT-IR as well as ESI-MS. X-ray diffraction reveals solids-state structures of Cr2, Cr4 and Cr6 all adopt pseudo-octahedral coordination environment with respect to metal center. All complexes have been tested in stereoregulated polymerization of butadiene under various polymerization conditions. The trans-1,4 and cis-1,4 enchainment of resultant polymer are found to be dependent on the structure of ligand and amount of activator used. Under the optimized condition, free ortho-substitutes Cr catalysts Cr1, Cr3, Cr4 and Cr6 are capable of initiating high trans-1,4 selectivity (trans-1,4: 89.2%-92.0%) with good polymer yields (71.5%-78.0%), while counterparts with ortho-positioned alkyl groups Cr2, Cr5 and Cr7 display mixed selectivities with moderate polymer yields. The sterical effect of ligand and amount of MMAO on the catalytic performance, in particular, the stereoselectivity and polymer yield, has been also elucidated by conjugated diene polymerization mechanism. © 2014 Elsevier B.V. All rights reserved.

  9. 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.

  10. Surface modification of halloysite nanotubes by vulcanization accelerator and properties of styrene-butadiene rubber nanocomposites with modified halloysite nanotubes

    Science.gov (United States)

    Zhong, Bangchao; Jia, Zhixin; Hu, Dechao; Luo, Yuanfang; Guo, Baochun; Jia, Demin

    2016-03-01

    Vulcanization accelerant N-cyclohexyl-2-benzothiazole sulfenamide (CZ) was used as a surface modifier and chemically grafted on the surface of halloysite nanotubes (HNTs) to obtain CZ-functionalized HNTs (HNTs-s-CZ). It was found that HNTs-s-CZ could be homogeneously dispersed into styrene-butadiene rubber (SBR). The grafted CZ molecules, exactly located at the filler-rubber interface, reduced the activation energy of vulcanization of SBR/HNTs-s-CZ compounds. Besides, the density of chain segments introduced by the interfacial phase of SBR/HNTs-s-CZ nanocomposites was higher than the other nanocomposites with silane-modified HNTs (m-HNTs) or pristine HNTs, manifesting an indication of enhanced filler-rubber interfacial interaction in SBR/HNTs-s-CZ nanocomposites. Consequently, SBR/HNTs-s-CZ nanocomposites showed excellent mechanical properties. The tensile strength could be enhanced by as much as 38.6% and 102.5% compared to those of SBR/m-HNTs and SBR/HNTs nanocomposites, respectively, though containing equivalent accelerant component. The value of this work lies in the fact that apparent properties improvement of elastomer composites has been achieved by the incorporation of vulcanization accelerant-functionalized HNTs, which may be fruitful for the rational design of filler surface treatment and offer new scientific and technological opportunities for the preparation of high performance elastomer composites.

  11. Research of operational properties of compound based on high viscosity styrene-butadiene rubber SSBR-2560 TDAE HV

    Directory of Open Access Journals (Sweden)

    M. I. Falyakhov

    2016-01-01

    Full Text Available The article consider the influence of replacement of SSBR-2560 TDAE batch production on high viscosity SSBR-2560-TDAE HV in the tread recipe on the tire performance properties. Obtained samples were highly viscosity styrene butadiene rubber did not differ in the microstructure of the SSBR-2560 TDAE batch production. Increasing the molecular weight possible to increase the Mooney viscosity of the rubber, however, is known to one of adverse factors is the deterioration of processability of rubber compounds based on polymers. In this connection, investigated the behavior in the step mixing compound based on high viscosity SSBR rubber. We chose recipes tread of the tire with a high content of organic silicon filler. It is established that the equivalent replacement of the polymer in the tread recipe does not lead to significant changes in the basic parameters of rubber mixing. We observed a slight increase in the energy consumption for the preparation of the rubber compounds, as well as the discharge temperature at each stage. It was shown to improve the distribution of the filler in the polymer matrix for the compound based on SSBR-2560 TDAE HV. The results showed that compound based on high viscosity SSBR improves rolling resistance and traction characteristics, while maintaining abrasion in comparison with the SSBR-2560-M27 batch production. Recommended use this brand in the production of rubber car tires.

  12. 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.

  13. Influence of gamma irradiation on mechanical and thermal properties of waste polyethylene/nitrile butadiene rubber blend

    Directory of Open Access Journals (Sweden)

    Raouf O. Aly

    2016-11-01

    Full Text Available Gamma irradiation radical–radical interaction crosslinking of elastomers and thermoplastic is a special type of crosslinking technique that has gained importance over conventional chemical crosslinking method as process is fast, pollution free, and simple. In this work a blend polymer, based on waste polyethylene and nitrile butadiene rubber, has been irradiated with gamma-rays, mechanically and thermally investigated at varying NBR content. FTIR and SEM techniques were used in addition to the swelling behavior to emphasize the blend formation. Mechanical properties like tensile strength, elongation at break and modulus at different elongations were studied and compared with those of unirradiated ones. A relatively low-radiation dose was found effective in improving the level of mechanical properties. Differential scanning calorimeter and thermogravimetric analysis were used to study the thermal characteristics of the irradiated polymer. Enhancement in thermal stability has been observed for higher NBR containing blends and via radiation-induced crosslinking up to ≈50 kGy.

  14. Plane-interface-induced lignin-based nanosheets and its reinforcing effect on styrene-butadiene rubber

    Directory of Open Access Journals (Sweden)

    C. Jiang

    2014-09-01

    Full Text Available Lignin was viewed as a spherical microgel in aqueous alkali. While spread out in a monolayer or adsorbed on a surface, lignin was made up of flexible, disk-like molecules with approximately the same thickness of 2 nm. According to this principle, we employed the lamina of montmorillonite (MMT as a plane template to anchor cationic lignin (CL on its two sides, resulting in the formation of CL-MMT hybrid materials (CLM. The isotherm adsorption behavior and structure characteristics of CLM were studied. The results showed that CLM was individually dispersed nanosheets with a thickness of about 5 nm when the mass ratio of CL to MMT is more than 2:1 and prepared at acidic or neutral pH. Compared to the cocoagulation of lignin and styrene-butadiene rubber (SBR, CLM obviously accelerated the coagulation rate, due to the reduction of surface activity of CL restricted by MMT. The nanoscale dispersion of CLM in SBR matrix significantly improved the tensile strength of CLM/SBR nanocomposites to 14.1 MPa by adding only 10 phr CLM and cardanol glycidyl ether (CGE as compatibilizer. Dynamic mechanical analysis (DMA showed that the glass transition temperature of SBR/CLM nanocomposites decreased with increasing CLM loading. Correspondingly, a special interfacial structure was proposed.

  15. Degree of Mechanochemical Devulcanization of Model Styrene-Butadiene Rubber Compounds Containing Different Amount of Poly-, Di- and Monosulphidic Bonds

    Science.gov (United States)

    Sangari, Samra; Anita, Hill; Dumitru, Pavel

    2004-03-01

    There have been significant attempts to devulcanize waste elastomers to facilitate reusing these valuable resources in applications requiring the unique properties of rubber. The difficulty in recycling of elastomers has traditionally been with devulcanizing the elastomer without comprising its properties due to degradation of main chains. This research aimed to devulcanize model styrene-butadiene rubber (SBR) compounds, which had various amounts of poly-, di- and monosulfidic crosslinks using a mechanochemical process. Three model compounds were prepared using SBR using a laboratory two-roll mill. They were then vulcanized in a compression molding press at 140r C. The prepared vulcanized compounds were then ground and devulcanized in an internal mixer using a chemical mixture at a constant rotor speed and temperature. The crosslink density of the compounds before and after the devulcanization was calculated using volume-swelling measurements. The obtained data was used to establish the correlation between crosslink density of the compounds and the degree of devulcanization. The results showed that mechanochemical devulcanization caused a significant decrease in the crosslink density of the compounds by breaking the sulfidic linkages. The break up of polysulfidic crosslinks was predominant, meaning that mechanochemical process selectively affected different types of crosslinks.

  16. Denitrification with acrylonitrile as a substrate using pure bacteria cultures isolated from acrylonitrile-butadiene-styrene wastewater.

    Science.gov (United States)

    Wang, C C; Lee, C M

    2001-04-01

    This study attempted to isolate and identify the denitrifying bacteria that utilize acrylonitrile as a substrate from acrylonitrile-butadiene-styrene (ABS) resin wastewater. The performance of the denitrifying bacteria for treating different initial acrylonitrile concentrations was also investigated under anoxic conditions. The results showed that seven strains of denitrifying bacteria that can use acrylonitrile or acrylic acid as a substrate were isolated from the denitrification tank of a wastewater treatment plant in a ABS resin manufacturing plant and a lab-scale anoxic granular activated carbon-fluidized bed. The bacteria strains Acidovorax facilis B and Pseudomonas nautica could utilize acrylonitrile up to 279 mg/l as a substrate for denitrification. For complete nitrate removal, an adequate supply of acrylonitrile was necessary. Under the assumption that the acrylic acid would be completely removed, the removal of 1 mg/l nitrate by A. facilis B or P. nautica, about 0.64-0.74 mg/l acrylonitrile or 0.87-1 mg/l acrylic acid was needed. Because strains A. facilis B and P. nautica could utilize acrylonitrile for denitrification, they are expected to play an important role in the treatment of acrylonitrile in the wastewater treatment plant (denitrification and nitrification processes) and lab-scale granular activated carbon-fluidized bed.

  17. Isolation of the epsilon-caprolactam denitrifying bacteria from a wastewater treatment system manufactured with acrylonitrile-butadiene-styrene resin.

    Science.gov (United States)

    Wang, Chun-Chin; Lee, Chi-Mei

    2007-06-25

    epsilon-Caprolactam has high COD and toxicity, so its discharge to natural water and soil systems may lead to an adverse environmental effect on water quality, endangering public health and welfare. This investigation attempts to isolate epsilon-caprolactam denitrifying bacteria from a wastewater treatment system manufactured with acrylonitrile-butadiene-styrene (ABS) resin. The goal is to elucidate the effectiveness of isolated pure strain and ABS mixed strains in treating epsilon-caprolactam from synthetic wastewater. The results reveal that Paracoccus versutus MDC-3 was isolated from the wastewater treatment system manufactured with ABS resin. The ABS mixed strains and P. versutus MDC-3 can consume up to 1539mg/l epsilon-caprolactam to denitrify from synthetic wastewater. Complete epsilon-caprolactam removal depended on the supply of sufficient electron acceptors (nitrate). Strain P. versutus MDC-3, Hyphomicrobium sp. HM, Methylosinus pucelana and Magnetospirillum sp. CC-26 are related closely, according to the phylogenetic analyses of 16S rDNA sequences.

  18. Use of an acrylonitrile-butadiene-styrene (ABS) plastic ring as a matrix in the recovery of bite mark evidence.

    Science.gov (United States)

    Sweet, D J; Bastien, R B

    1991-09-01

    Valuable forensic information can be obtained from analysis of human bite mark injuries after careful retrieval of such evidence from living or deceased victims. It is difficult, however, to maintain the anatomical configuration of the skin, especially where body contours complicate the recovery process. Transillumination of the injury pattern in the skin after removal and preservation of the tissue from a deceased victim can provide significant information in the investigation process. A dimensionally stable matrix is required to support the skin's anatomical configuration during and after its removal. The authors have developed a unique and convenient method of heating and contouring a ring of acrylonitrile-butadiene-styrene (ABS) plastic using table salt over a heat source. When this ring is applied to the deceased victim's skin, and a backing material is added for support, removal of the skin and the bite mark can be accomplished more predictably while maintaining the anatomical contour. It is important to record bite marks accurately as soon after discovery as possible; the authors believe that this technique will significantly aid recovery of such evidence either at the crime scene or in the laboratory. A method of inscribing appropriate anatomical markers and case numbers on the rings is also described.

  19. Denitrification with acrylamide by pure culture of bacteria isolated from acrylonitrile-butadiene-styrene resin manufactured wastewater treatment system.

    Science.gov (United States)

    Wang, C C; Lee, C M

    2001-08-01

    Acrylamide is widely used in industrial applications as cement binder and solidification agent. Due to its carcinogenicity and toxicity, discharge of acrylamide to the natural water and soil systems may lead to an adverse environmental impact on water quality and thus endanger public health and welfare. This study attempts to isolate and identify the denitrifying bacteria, which utilize acrylamide as the substrate from the acrylonitrile-butadiene-styrene resin manufactured wastewater treatment system. The performance of the denitrifying bacteria for treating different initial acrylamide concentrations was also investigated under aerobic and anaerobic conditions. The test results indicated that the Pseudomonas stutzeri could remove acrylamide at concentrations below 440 mg/l under aerobic conditions. The acrylic acid and ammonia intermediates were used as carbon and nitrogen sources, respectively. However, P. stutzeri did not show the capability of metabolizing acrylonitrile under aerobic conditions. Furthermore, the P. stutzeri could utilize both acrylamide and acrylic acid in the presence of nitrate (denitrification) and acrylamide could be removed completely from the wastewater.

  20. Effects of heat treatments and UV exposures on mechanical properties of 3D printed acrylonitrile butadiene styrene specimens

    Science.gov (United States)

    Hughes, Shawn M.; Alamir, Mohammed; Neas, Brian; Alzahrani, Naif; Asmatulu, Ramazan

    2017-04-01

    Over the last few years, tremendous amount of research efforts has been conducted on 3D printing materials, methods and systems. Various 3D printer materials in different size, shape and geometry can be used for advanced designs, modeling, and manufacturing for different industrial applications. In the present study, dog bone shape specimen was designed via a CATIA CAD model, and then printed by a 3D printer using a polymeric filament (acrylonitrile butadiene styrene - ABS). Some of the prepared samples were heat treated at 40 °C, 60 °C, and 80 °C for 30 minutes, while the others were exposed to the UV light in a chamber for 0, 5, 10, 15 and 20 days. The surface and mechanical properties of the conditioned samples were determined using water contact angle and tensile test units, respectively. The test results indicated that the heat treatment process increased the mechanical properties; however, the UV exposure tests significantly reduced the water contact angle and properties of the samples. During these studies, undergraduate engineering students were involved in the tests, and gained a lot of hands-on research experiences.

  1. 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.

  2. Wear resistance and friction reduction in acrylo nitrile butadiene rubber through hybrid combination of graphite flakes and nano tungsten disulphide

    Energy Technology Data Exchange (ETDEWEB)

    Agrawal, Neha, E-mail: neha87bhu@gmail.com [Defence Material Store Research Development and Establishment (DMSRDE), DRDO, GT Road, Kanpur 208013, U.P (India); Indian Institute of Technology Bombay, Powai, Mumbai 400076, Maharashtra (India); Pandey, Akanksha; Parihar, A. S.; Mishra, A. K.; Mukhopadhyay, K.; Prasad, N. E. [Defence Material Store Research Development and Establishment (DMSRDE), DRDO, GT Road, Kanpur 208013, U.P (India); Gandhi, M. N.; Bhattacharyya, A. R. [Indian Institute of Technology Bombay, Powai, Mumbai 400076, Maharashtra (India)

    2016-05-06

    Friction and wear have considerable role in the life span of two interacting parts. Incorporation of nanofillers in polymers/elastomers matrix causes commendable changes in its tribologicalproperties. The main purpose of this work is to reduce the coefficient of friction and wear rate of Acrylo Nitrile Butadiene rubber (NBR). To achieve such objective traditionally well knownlubricants graphite(G), tungsten disulphide (WS{sub 2}) and there hybrid combination was incorporated in NBR matrix. Effect of applied load (force) and concentration of fillers on tribological properties of NBR had been studied. The filler incorporation enhanced the hardnessby 8%, showed resistance to hydraulic oil and aging effect also got improved significantly. A particular optimized concentration of NBR with hybrid combination of 2% WS{sub 2} and 4% Graphite showed minimum coefficient of friction as well as wear rate. A hypothesis could be attributed that similar lamellar structure of WS{sub 2} and Graphite along with formation of a stable nanoscale disulfide tribofilmcould result in lowering of friction. These substantially improved properties of nanoreinforced rubber materials would definitely pave promising path for plethora of potential technological applications.

  3. Gas Uptake of 3-D Printed Acrylonitrile Butadiene Styrene (ABS) Using a Vacuum Apparatus Designed for Absorption and Desorption Studies.

    Science.gov (United States)

    Sefa, Makfir; Ahmed, Zeeshan; Fedchak, James A; Scherschligt, Julia; Klimov, Nikolai

    2016-11-01

    We describe a vacuum apparatus for determining the outgassing rate into vacuum, the diffusion coefficient, and the amount of gas absorbed for various materials. The diffusion coefficient is determined from a model applied to time-dependent desorption data taken using a throughput method. We used this method to determine the diffusion coefficient, D, for H2O in 3-D printed acrylonitrile butadiene styrene (ABS). We found DH2O = 8.3 × 10-8 cm2/s ± 1.3 × 10-8 cm2/s (k = 1; 67% confidence interval) at 23.2 °C. This result was compared to the diffusion coefficient determined another by a gravimetric method, in which the sample weight was monitored as it absorbed gas from the atmosphere. The two methods agreed to within 3%, which is well within the uncertainty of the measurement. We also found that at least 80% of the atmospheric gas (air) absorbed by the ABS is water. The total amount of all atmospheric gas absorbed by ABS was about 0.35% by weight when exposed to ambient air in the laboratory, which was at a pressure of 101 kPa with a relative humidity of 57% at 22.2 °C.

  4. Separation of polycarbonate and acrylonitrile-butadiene-styrene waste plastics by froth flotation combined with ammonia pretreatment.

    Science.gov (United States)

    Wang, Chong-Qing; Wang, Hui; Liu, Qun; Fu, Jian-Gang; Liu, You-Nian

    2014-12-01

    The objective of this research is flotation separation of polycarbonate (PC) and acrylonitrile-butadiene-styrene (ABS) waste plastics combined with ammonia pretreatment. The PC and ABS plastics show similar hydrophobicity, and ammonia treatment changes selectively floatability of PC plastic while ABS is insensitive to ammonia treatment. The contact angle measurement indicates the dropping of flotation recovery of PC is ascribed to a decline of contact angle. X-ray photoelectron spectroscopy demonstrates reactions occur on PC surface, which makes PC surface more hydrophilic. Separation of PC and ABS waste plastics was conducted based on the flotation behavior of single plastic. At different temperatures, PC and ABS mixtures were separated efficiently through froth flotation with ammonia pretreatment for different time (13 min at 23 °C, 18 min at 18 °C and 30 min at 23 °C). For both PC and ABS, the purity and recovery is more than 95.31% and 95.35%, respectively; the purity of PC and ABS is up to 99.72% and 99.23%, respectively. PC and ABS mixtures with different particle sizes were separated effectively, implying that ammonia treatment possesses superior applicability. Copyright © 2014 Elsevier Ltd. All rights reserved.

  5. DISTRIBUTION OF THE MIXTURE THROUGH THE REACTORS CASCADE IN THE PRODUCTION OF LOW MOLECULAR COPOLYMERS OF BUTADIENE WITH STYRENE

    Directory of Open Access Journals (Sweden)

    V. F. Lebedev

    2014-01-01

    Full Text Available Summary. In the polymerization of butadiene with styrene heat removal is the main factor limiting the output of the cascade reactor. Thus the residence time of the monomers in the reactor exceeds significantly the time necessary to complete the process on the basis of kinetic regularities. To increase the output of the mixture the distribution in the reactor cascade is made. It is necessary to distribute the flow of mixture through the reactor of the cascade to have the resulting polymer of the same viscosity at the outlet of each reactor. The algorithm of distribution of the mixture in the reactor cascade with regard to the synthesis parameters (temperature in the reactor and the feed rate of the mixture, the ratio of the modifier and the initiator in the complex, the number of reactors and a determined dynamic viscosity is developed. In accordance with the developed algorithm the calculation of the velocity of the mixture feed in each reactor of the cascade is made. It is shown that the flow of mixture in each polymerization unit depends on the overall output of the installation and the number of reactors in the cascade. The algorithm for the distribution of the initial mixture in the reactor cascade is developed to provide maximum output of the installation and set the quality of the obtained polymer. To determine the degree of conversion of monomers and temperature conditions of the process of polymerization under the calculated speed of the feed mixture in the first polymerization cascade the basic technological parameters of the polymerization process in real time mode, the calculation using a mathematical model is made. The analysis of the simulation results shows that during the first hour, the concentration of monomers does not exceed of 0.085 mol/l, which corresponds to the degree of conversion of monomer to 99 %, while the temperature in the reactor corresponds to the optimal mode - from 65 to 85 0C.

  6. Synthesis of mixed-ligand cobalt complexes and their applications in high cis-1,4-selective butadiene polymerization

    KAUST Repository

    Liu, Wen

    2015-08-03

    Incomplete oxidation of (N-di-tert-butylphosphino)-6-(2-methyl-2’H-benzoimidazole)-2-aminepyridine dichlorocobalt (PN3CoCl2) in DMF results in a unique co-crystal I formed with three parts including DMF, unit A and unit B complex with Co1 and Co2, respectively, (PN3 ligand in unit A: (N-di-tert-butylphosphino)-6-(2’-methyl-2’H-benzoimidazole)-2-aminepyridine, and O=PN3 ligand in unit B: (N-di-tert-butylphosphinoxide)-6-(2’-methyl-2’H-benzoimidazole)-2-aminepyridine) with 1:1:1 molar ratio. Co1 and Co2 complexes both display a five-coordinated distorted-square-pyramidal geometry around the metal center. The Co1 center is coordinated with PN3 ligand via two N atoms from pyridine, benzoimidazole moiety as well as one P atom, and the Co2 center is coordinated with the oxidized ligandO=PN3 via two N atoms from pyridine, benzoimidazole moiety as well as one O atom from DMF molecule, while the oxidized phosphine moiety (O=P) being excluded from the coordination sphere. Activated with AlEt2Cl, the co-crystallized complexes I are able to actively convert butadiene to polybutadiene, affording cis-1,4 polybutadiene with cis-1,4 unit up to 95.5-97.8% and number average molecular weight of cal. 105g/mol. The high cis-1,4 selectivity and monomodal GPC curve of resultant polymer imply that the identical active species generated from two distinctive cobalt centers.

  7. Hybrid joining of polyamide and hydrogenated acrylonitrile butadiene rubber through heat-resistant functional layer of silane coupling agent

    Energy Technology Data Exchange (ETDEWEB)

    Sang, Jing; Sato, Riku [Department of Frontier Materials and Function Engineering, Graduate School of Engineering, Iwate University, 4-3-5 Ueda, Morioka 020-8551 (Japan); Aisawa, Sumio, E-mail: aisawa@iwate-u.ac.jp [Department of Frontier Materials and Function Engineering, Graduate School of Engineering, Iwate University, 4-3-5 Ueda, Morioka 020-8551 (Japan); Hirahara, Hidetoshi [Department of Frontier Materials and Function Engineering, Graduate School of Engineering, Iwate University, 4-3-5 Ueda, Morioka 020-8551 (Japan); Mori, Kunio [Department of Frontier Materials and Function Engineering, Graduate School of Engineering, Iwate University, 4-3-5 Ueda, Morioka 020-8551 (Japan); Sulfur Chemical Institute, 210, Collabo MIU, 4-3-5, Ueda, Morioka 020-0066 (Japan)

    2017-08-01

    Highlights: • We modify PA6 surface using silane coupling agent layer of APTMS to link HNBR. • APTMS greatly improved heat resistance of PA6 from 153 °C up to 325 °C. • A PA6/HNBR joined body was obtained, and it exhibits high adhesion strength with cohesive failure. • Chemical structures of the adhesion interfaces of PA6/HNBR were confirmed by Nano-IR. - Abstract: A simple, direct adhesion method was developed to join polyamide (PA6) to hydrogenated acrylonitrile butadiene rubber (HNBR) by grafting a functional layer of a silane coupling agent on plasma functionalized PA6 surfaces. The functional layer of the silane coupling agent was prepared using a self-assembly method, which greatly improved the heat resistance of PA6 from 153 °C up to 325 °C and the resulting PA6/HNBR joints showed excellent adhesion properties with cohesive failure between PA6 and HNBR. X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), and nanoscale infrared microscopy and chemical imaging (Nano-IR, AFM-IR) were employed to characterize the surfaces and interfaces. The Nano-IR analysis method was employed for the first time to analyze the chemical structures of the adhesion interfaces between different materials and to establish the interface formation mechanism. This study is of significant value for interface research and the study of adhesion between resins and rubbers. There is a promising future for heat-resistant functional layers on resin surfaces, with potential application in fuel hose composite materials for the automotive and aeronautical industries.

  8. 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.

  9. Effect of magnetic and thermal properties of iron oxide nanoparticles (IONs) in nitrile butadiene rubber (NBR) latex

    Science.gov (United States)

    Ong, Hun Tiar; Julkapli, Nurhidayatullaili Muhd; Hamid, Sharifah Bee Abd; Boondamnoen, O.; Tai, Mun Foong

    2015-12-01

    Nitrile butadiene rubber (NBR) gloves are one of the most important personal protective equipments but they are possible to tear off and contaminate food or pharmaceutical and healthcare products during manufacturing and packaging process. High tendency of torn glove remaining in food or products due to white or light flesh-coloured glove is not easy to be detected by naked eyes. In this paper, iron oxide nanoparticles (IONs) selected as additive for NBR to improve its detectability by mean of magnetic properties. IONs synthesized via precipitation method and compounded with NBR latex before casting on petri dish. The properties of IONs were investigated by X-ray Diffractometry (XRD), Transmission Electron Microscope (TEM), Raman Spectroscopy and Vibrating Sample Magnetometer (VSM). Meanwhile NBR/IONs composites were studied by Thermogravimetry Analysis (TGA), Differential Scanning Calorimetry (DSC) and Vibrating Sample Magnetometer (VSM). It observed that, synthesized IONs shows of 25.28 nm crystallite with 25.86 nm semipherical (changed as) shape. Meanwhile, Magnetite and maghemite phase are found in range of 670 cm-1 and 700 cm-1 respectively, which it contributes magnetization saturation of 73.96 emu/g at 10,000 G by VSM. Thermal stability and magnetic properties were increased with incorporating IONs into NBR latex up to 20 phr. NBR/IONs 5 phr has the optimum thermal stability, lowest glass transition temperature (-14.83 °C) and acceptable range of magnetization saturation (3.83 emu/g at 10,000 G) to form NBR gloves with magnetic detectability.

  10. Surface modification of halloysite nanotubes by vulcanization accelerator and properties of styrene-butadiene rubber nanocomposites with modified halloysite nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Zhong, Bangchao; Jia, Zhixin, E-mail: zxjia@scut.edu.cn; Hu, Dechao; Luo, Yuanfang; Guo, Baochun; Jia, Demin

    2016-03-15

    Graphical abstract: - Highlights: • Vulcanization accelerant was used to modify halloysite nanotubes (HNTs). • The modified HNTs reduced the activation energy of vulcanization. • Strong filler–rubber interaction was achieved in rubber/modified HNTs composites. • The modified HNTs exhibited excellent reinforcement effect on rubber. - Abstract: Vulcanization accelerant N-cyclohexyl-2-benzothiazole sulfenamide (CZ) was used as a surface modifier and chemically grafted on the surface of halloysite nanotubes (HNTs) to obtain CZ-functionalized HNTs (HNTs-s-CZ). It was found that HNTs-s-CZ could be homogeneously dispersed into styrene-butadiene rubber (SBR). The grafted CZ molecules, exactly located at the filler-rubber interface, reduced the activation energy of vulcanization of SBR/HNTs-s-CZ compounds. Besides, the density of chain segments introduced by the interfacial phase of SBR/HNTs-s-CZ nanocomposites was higher than the other nanocomposites with silane-modified HNTs (m-HNTs) or pristine HNTs, manifesting an indication of enhanced filler-rubber interfacial interaction in SBR/HNTs-s-CZ nanocomposites. Consequently, SBR/HNTs-s-CZ nanocomposites showed excellent mechanical properties. The tensile strength could be enhanced by as much as 38.6% and 102.5% compared to those of SBR/m-HNTs and SBR/HNTs nanocomposites, respectively, though containing equivalent accelerant component. The value of this work lies in the fact that apparent properties improvement of elastomer composites has been achieved by the incorporation of vulcanization accelerant-functionalized HNTs, which may be fruitful for the rational design of filler surface treatment and offer new scientific and technological opportunities for the preparation of high performance elastomer composites.

  11. Damping of Mechanical Waves with Styrene/Butadiene Rubber Filled with Polystyrene Particle: Effects of Particles Size and Wave Frequency

    Directory of Open Access Journals (Sweden)

    M. Haghgo

    2007-08-01

    Full Text Available Utilizing polymeric materials for damping mechanical waves is of great importance in various fields of applications such as military camouflage, prevention of structural vibrational energy transfer, and noise attenuation. This ability originates from segmental dynamics of chain-like polymer molecules. Damping properties of styrene-butadiene rubbercontaining 10 wt% of monosize polystyrene particles with different diameters (from 80 nm to 500 μm was investigated in the frequency range of vibration, sound, and ultrasound via dynamic mechanical thermal analysis, normalsound adsorption test, and ultrasound attenuation coefficient measurement. The obtained results indicated that for different systems, containing different sizes of polystyrene particles, the area under the damping curve does not show significant change comparing to the neat SBR in the frequency range studied. However, addition of polystyrene particles, specifically nanosized particles, resulted in emergence of a secondary glass transition temperature which could be attributed to the modified dynamics of a layer of matrix molecules near the surface of PS particles. In the range of sound frequency, 0.5 to 6.3 kHz, the maximum damping was observed for the system containing polystyrene nanoparticles. However the single damping curve of neat SBR was separated into two or even three distinct curves owing to the presence of the particles. The maximum damping in the ultrasound frequency range was found for the system containing 0.5 mm polystyrene particles. This is attributed to different contributions from matrix chains dynamics and the reflection of mechanical waves from particles-matrix interface at different frequency ranges. On other words, the increase in the glass transition temperature of the elastomeric matrix phase with increasing the mechanical wave frequency causes a reduction in the contribution from matrix chains dynamics while the contribution due to diffraction from dispersed

  12. 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.

  13. Dynamics of phase separation in poly(acrylonitrile-butadiene-styrene)-modified epoxy/DDS system: kinetics and viscoelastic effects.

    Science.gov (United States)

    Jyotishkumar, P; Özdilek, Ceren; Moldenaers, Paula; Sinturel, Christophe; Janke, Andreas; Pionteck, Jürgen; Thomas, Sabu

    2010-10-28

    The dynamics of phase separation and final morphologies of poly(acrylonitrile-butadiene-styrene) (ABS)-modified epoxy system based on diglycidyl ether of bisphenol A (DGEBA) cured with 4,4'-diaminodiphenylsulfone (DDS) have been monitored in situ throughout the entire curing process by using optical microscopy (OM), differential scanning calorimetry (DSC), rheometry, and small-angle laser light scattering (SALLS). The evolution of phase separation and final morphologies with substructures were explored by OM. The final morphologies of the blend cured at 150 and 165 °C are of phase-inverted type and are quite different from the final morphologies of the same blend cured at 180 °C, in which the final morphologies are cocontinuous. AFM observations of the fully cured sample confirmed the existence of three different phases, the epoxy continuous phase, SAN (styrene/acrylonitrile) continuous phase, and PB droplets at the interface, with a strong tendency to stay at SAN continuous phase. Furthermore, the continuous epoxy phase contains SAN particles and the continuous SAN phase contains epoxy particles. Cure kinetics and rheological results correspond well with the viscoelastic phase separation revealed by OM. The SALLS results display clearly that the phase separation takes place according to nucleation and growth mechanism followed by spinodal decomposition. The development of light scattering patterns during the second stage phase separation follows the Cahn-Hilliard model of spinodal demixing. Furthermore, the evolution of the scattering vector follows a Maxwell-type relaxation equation establishing the viscoelastic behavior of phase separation. The relaxation time of phase separation can be described by the Williams-Landel-Ferry equation for viscoelasticity. As a whole, the dependence of phase separation on cure temperature and the development of final morphologies and the associated mechanisms were explored in detail for the complex epoxy/ABS system.

  14. The influence of mechanical properties in the electrical breakdown in poly-styrene-ethylene-butadiene-styrene thermoplastic elastomer

    Science.gov (United States)

    Kollosche, Matthias; Melzer, Michael; Becker, Andre; Stoyanov, Hristian; McCarthy, Denis N.; Ragusch, Hülya; Kofod, Guggi

    2009-03-01

    Dielectric elastomer actuators (DEA) are a class of eletro-active polymers with promising properties for a number of applications, however, such actuators are prone to failure. One of the leading failure mechanisms is the electrical breakdown. It is already well-known that the electro-mechanical actuation properties of DEA are strongly influenced by the mechanical properties of the elastomer and compliant electrodes. It was recently suggested that also the electrical breakdown in such soft materials is influenced by the mechanical properties of the elastomer. Here, we present stress-strain measurements obtained on two tri-block thermoplastic elastomers (SEBS 500040 and SEBS 500120, poly-styrene-ethylene-butadiene-styrene), with resulting large differences in mechanical properties, and compare them to measurements on the commonly used VHB 4910. Materials were prepared by either direct heat-pressing of the raw material, or by dissolving in toluene, centrifuging and drop-casting. Experiments showed that materials prepared with identical processing steps showed a difference in stiffness of about 20%, where centrifuged and drop-casted films were seen to be softer than heat-pressed films. Electric breakdown measurements showed that for identically processed materials, the stiffness seemed to be a strong indicator of the electrical breakdown strength. It was therefore found that processing leads to differences in both stiffness and electrical breakdown strength. However, unexpectedly, the softer drop-cast films had a much higher breakdown strength than the heatpressed films. We attribute this effect to impurities still present in the heat-pressed films, since these were not purified by centrifuging.

  15. Structure Sensitivity in Pt Nanoparticle Catalysts for Hydrogenation of 1,3-Butadiene: In Situ Study of Reaction Intermediates Using SFG Vibrational Spectroscopy

    KAUST Repository

    Michalak, William D.

    2013-01-31

    The product selectivity during 1,3-butadiene hydrogenation on monodisperse, colloidally synthesized, Pt nanoparticles was studied under reaction conditions with kinetic measurements and in situ sum frequency generation (SFG) vibrational spectroscopy. SFG was performed with the capping ligands intact in order to maintain nanoparticle size by reduced sintering. Four products are formed at 75 C: 1-butene, cis-2-butene, trans-2-butene, and n-butane. Ensembles of Pt nanoparticles with average diameters of 0.9 and 1.8 nm exhibit a ∼30% and ∼20% increase in the full hydrogenation products, respectively, as compared to Pt nanoparticles with average diameters of 4.6 and 6.7 nm. Methyl and methylene vibrational stretches of reaction intermediates observed under working conditions using SFG were used to correlate the stable reaction intermediates with the product distribution. Kinetic and SFG results correlate with previous DFT predictions for two parallel reaction pathways of 1,3-butadiene hydrogenation. Hydrogenation of 1,3-butadiene can initiate with H-addition at internal or terminal carbons leading to the formation of 1-buten-4-yl radical (metallocycle) and 2-buten-1-yl radical intermediates, respectively. Small (0.9 and 1.8 nm) nanoparticles exhibited vibrational resonances originating from both intermediates, while the large (4.6 and 6.7 nm) particles exhibited vibrational resonances originating predominately from the 2-buten-1-yl radical. This suggests each reaction pathway competes for partial and full hydrogenation and the nanoparticle size affects the kinetic preference for the two pathways. The reaction pathway through the metallocycle intermediate on the small nanoparticles is likely due to the presence of low-coordinated sites. © 2012 American Chemical Society.

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

    OpenAIRE

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

    2014-01-01

    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...

  17. The use of styrene-butadiene rubber waste as a potential filler in nitrile rubber: order of addition and size of waste particles

    OpenAIRE

    Baeta,D. A.; Zattera,J. A.; Oliveira,M. G.; Oliveira,P. J.

    2009-01-01

    Styrene-butadiene rubber (SBR) has large applications in the shoe industry, especially as expanded sheets used to produce insoles and inner soles. According to TG analysis, the rubber content in SBR residues (SBR-r) was found to be around 26-wt%. Based on that data, a cost-effective technique for the reuse of SBR-r in Nitrile rubber (NBR) was developed. Later, the effect of SBR-r on the cure behavior, mechanical performance, swelling, and crosslink density of reused rubber was investigated, w...

  18. Gas chromatographic head-space determination of residual acrylonitrile in acrylonitrile-butadiene-styrene resins and migration into a simulated fatty foodstuffs liquid.

    Science.gov (United States)

    Di Pasquale, G; Di Iorio, G; Capaccioli, T

    1978-10-11

    Head-space methods are described for the determination of residual acrylonitrile in acrylonitrile-butadiene-styrene resins and in olive oil, which simulates fatty foodstuffs. Dimethylformamide was used as solvent for the resin, with flame ionization detection. The injection of water into the resin dispersion prior to head-space analysis greatly enhances the detection capabilities. The use of a nitrogen-selective detector required dimethyl sulphoxide as the solvent. The determination of acrylonitrile in olive oil was carried out employing both types of detector. The detection sensitivity was much greater with the nitrogen-selective detector.

  19. Gas chromatographic-mass spectrometric analysis of some potential toxicants amongst volatile compounds emitted during large-scale thermal degradation of poly(acrylonitrile-butadiene-styrene) plastic.

    Science.gov (United States)

    Shapi, M M; Hesso, A

    1991-01-02

    A number of compounds emitted during the thermal degradation of plastics are potentially toxic. This study was aimed at identifying the volatile compounds emitted during large-scale thermal degradation of poly(acrylonitrile-butadiene-styrene). About 5 g of the sample were degraded at between 25 and 470 degrees C in air and nitrogen in a device that can simulate temperature-programmed thermogravimetry. The volatiles were collected in dichloromethane using the solvent trap technique. Some of the 92 compounds identified by gas chromatography-mass spectrometry were found to have no hitherto documented toxicological profiles, even though they are potentially dangerous.

  20. A computational study of the Diels-Alder reactions between 2,3-dibromo-1,3-butadiene and maleic anhydride

    Science.gov (United States)

    Rivero, Uxía; Meuwly, Markus; Willitsch, Stefan

    2017-09-01

    The neutral and cationic Diels-Alder-type reactions between 2,3-dibromo-1,3-butadiene and maleic anhydride have been computationally explored as the first step of a combined experimental and theoretical study. Density functional theory calculations show that the neutral reaction is concerted while the cationic reaction can be either concerted or stepwise. Further isomerizations of the Diels-Alder products have been studied in order to predict possible fragmentation pathways in gas-phase experiments. Rice-Ramsperger-Kassel-Marcus (RRKM) calculations suggest that under single-collision experimental conditions the neutral product may reform the reactants and the cationic product will most likely eliminate CO2.

  1. Comparison of two-body and three-body decomposition of ethanedial, propanal, propenal, n-butane, 1-butene, and 1,3-butadiene.

    Science.gov (United States)

    Chin, Chih-Hao; Lee, Shih-Huang

    2012-01-14

    We investigated two-body (binary) and three-body (triple) dissociations of ethanedial, propanal, propenal, n-butane, 1-butene, and 1,3-butadiene on the ground potential-energy surfaces using quantum-chemical and Rice-Ramsperger-Kassel-Marcus calculations; most attention is paid on the triple dissociation mechanisms. The triple dissociation includes elimination of a hydrogen molecule from a combination of two separate terminal hydrogen atoms; meanwhile, the rest part simultaneously decomposes to two stable fragments, e.g., C(2)H(4), C(2)H(2), or CO. Transition structures corresponding to the concerted triple dissociation were identified using the B3LYP/6-311G(d,p) level of theory and total energies were computed using the method CCSD(T)/6-311+G(3df, 2p). The forward barrier height of triple dissociation has a trend of ethanedial butane butane, 1-butene, and 1,3-butadiene were investigated for the first time. To outline a whole picture of dissociation mechanisms, some significant two-body dissociation channels were investigated for the calculations of product branching ratios. The triple dissociation plays an important role in the three carbonyl compounds, but plays a minor or negligible role in the three hydrocarbons.

  2. Preparation, characterization and evaluation of proton-conducting hybrid membranes based on sulfonated hydrogenated styrene-butadiene and polysiloxanes for fuel cell applications

    Energy Technology Data Exchange (ETDEWEB)

    Monroy-Barreto, M.; Aguilar, J.C.; Rodriguez de San Miguel, E.; de Gyves, J. [Departamento de Quimica Analitica, Facultad de Quimica, UNAM, Ciudad Universitaria, 04360 Mexico, D.F. (Mexico); Acosta, J.L.; del Rio, C.; Ojeda, M.C. [Instituto de Ciencia y Tecnologia de Polimeros (CSIC), c/Juan de la Cierva 3, 28006 Madrid (Spain); Munoz, M. [Departament de Quimica Analitica, Facultat de Ciencies, U.A.B., Bellaterra 08193 Barcelona (Spain)

    2010-12-15

    This paper describes the preparation of proton-conducting hybrid membranes (HMs) obtained by a solvent casting procedure using a solution containing sulfonated hydrogenated styrene-butadiene (HSBS-S) and an inorganic-organic mixture (polysiloxanes) previously prepared by a sol-gel route. HSBS-S copolymers with different sulfonation degrees were obtained and characterized by means of elemental analysis (EA), chemical titration and electrochemical impedance spectroscopy (EIS). HSBS-S with the best properties in terms of proton conductivity and solubility for the casting procedure was selected to prepare the HMs. The solvent casting procedure permitted the two phases to be homogeneously distributed while maintaining a relatively high proton conductivity in the membrane. HMs with different blend ratios were characterized using structural (Fourier transform infrared-attenuated total reflectance (FTIR-ATR), dynamic mechanical analysis (DMA), differential scanning calorimetry (DSC)), electrical (EIS), physicochemical (water uptake, ion-exchange capacity) and thermal (TGA-MS) methods. Finally, the optimized HSBS-S membrane and HMs were tested in hydrogen single fuel cells to obtain the polarization and power curves at different cell temperatures and gas pressures. Results indicate that HMs show a considerable improvement in performance compared to the optimized HSBS-S membrane denoting the benefit of incorporating the inorganic-organic network in the hydrogenated styrene-butadiene matrix. A Nafion membrane was used as reference material throughout this work. (author)

  3. Selective hydrogenation of 1,3-butadiene from crude C{sub 4} cracker stream with a solid catalyst with ionic liquid layer (SCILL). DSC and solubility study

    Energy Technology Data Exchange (ETDEWEB)

    Mangartz, T.; Korth, W.; Kern, C.; Jess, A. [Bayreuth Univ. (Germany). Dept. of Chemical Engineering

    2013-11-01

    In petroleum as well as in fine chemical industry, selective catalytic hydrogenation is an important reaction. The selective hydrogenation of 1,3-butadiene (BD) to butene (trans-,1- and cis-butene) from the crude C4 steam cracker fraction represents one example, but under today's technical conditions undesired butane forms inevitably in relevant amounts. To increase the butene yield, the concept of Solid Catalyst with Ionic Liquid Layer (SCILL) was employed. The SCILL catalyst, in contrast to the uncoated catalyst, yielded a remarkably high selectivity to butenes (S{sub butenes} > 99 %) even at high residence times or at high hydrogen partial pressure. Nearly no butane (S{sub butane} {approx} 0 %) was analytically detected. We expected that due to different solubility, the poorer soluble compounds discharged from the ionic liquid and, thus, caused the shift in selectivity to a great extent. Temperature dependent solubility measurements in the used ionic liquid ([DMIM][DMP]) revealed that the order of increasing solubility is 1,3-butadiene > butenes > butane which matches the assumption. However, since differences in solubility cannot explain this SCILL effect satisfyingly, ionic liquids are expected to affect the surface of the catalyst (side-specific ligand-type effect). Investigations using spectroscopic methods (e.g. FTIR) confirmed this suggestion. (orig.)

  4. 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.

  5. Sperm-head morphology study in B6C3F1 mice following inhalation exposure to 1,3-butadiene: Final technical report

    Energy Technology Data Exchange (ETDEWEB)

    Hackett, P.L.; McClanahan, B.J.; Brown, M.G.; Buschbom, R.L.; Clark, M.L.; Decker, J.R.; Evanoff, J.J.; Rommereim, R.L.; Rowe, S.E.; Westerberg, R.B.

    1988-04-01

    The present report describes the results of a study of the morphology of epididymal sperm heads of B6C3F1 mice that were exposed to varying concentrations of 1,3-butadiene. During the fifth post-exposure week, the animals were killed and examined for gross lesions of the reproductive tract; suspensions of the epididymal sperm were prepared for morphologic evaluations. No mortality was observed in any of the inhalation exposure groups. Transient toxic signs, including piloerection and dyspnea, were evident during a 20- to 30-minute period following exposure to 5000 ppM. Mean values for body weights and weight gains of the mice exposed to 1,3-butadiene were not significantly different from control values. A concentration-related increase in the incidence of sperm-head abnormalities was evident and the percentage of sperm heads that were morphologically abnormal was significantly higher in mice exposed to 1000 and 5000 ppM than in the controls. 23 refs., 2 figs., 6 tabs.

  6. Untapped potentials of acrylonitrile-butadiene-styrene/polyurethane (ABS/PU) blend membrane to purify dye wastewater.

    Science.gov (United States)

    Mandegari, Mansoor; Fashandi, Hossein

    2017-07-15

    Production of acrylonitrile-butadiene-styrene/polyurethane (ABS/PU) blend membrane with high rejection efficiency for disperse and vat dyes, is introduced as a facile and cost effective technique to purify textile wastewater. In this respect, membranes are produced using commercially available polymers, i.e. ABS and PU, with different compositions (ABS/PU: 100/0, 80/20, 70/30, 60/40 and 50/50 w/w) through wet casting. Casting solutions with concentration of 30 wt% are prepared using two different solvents, i.e. dimethylformamide (DMF) and N-methyl-2- pyrrolidone (NMP). The prepared membranes are characterized using a variety of analytical techniques including SEM imaging, FTIR spectroscopy, dry and wet gas permeation, evaluation of reusability, antifouling and mechanical properties, photostability, surface hydrophilicity and pure water permeability (PWP) of the produced membranes. According to the results, irrespective of solvent type, ABS/PU membranes with higher PU content have lower porosity and smaller pore size both of which contribute to enhanced dye rejection efficiency. This is while the impact of PU content on the photostability of ABS/PU membranes was found to be negligible. Additionally, the produced ABS/PU membranes exhibit good reusability and antifouling properties. However, the mechanical properties of ABS/PU membranes with higher PU contents are inferior to those with lower PU contents. This contrast highlights the prominence of optimum PU content to make a trade-off between dye rejection efficiency and mechanical properties. In this regard, ABS/PU (60/40 w/w) membrane is recognized as the one with optimum composition. Furthermore, it was found that regardless of PU content, membranes cast from DMF-based solutions exhibit superior rejection performance over those cast from NMP-based solutions. Overall, one can witness that employing ABS/PU membranes provides a meritorious and clean approach to refine disperse and vat dye wastewaters, a great threat

  7. Effect of magnetic and thermal properties of iron oxide nanoparticles (IONs) in nitrile butadiene rubber (NBR) latex

    Energy Technology Data Exchange (ETDEWEB)

    Ong, Hun Tiar; Julkapli, Nurhidayatullaili Muhd; Hamid, Sharifah Bee Abd, E-mail: sharifahbee@um.edu.my; Boondamnoen, O.; Tai, Mun Foong

    2015-12-01

    Nitrile butadiene rubber (NBR) gloves are one of the most important personal protective equipments but they are possible to tear off and contaminate food or pharmaceutical and healthcare products during manufacturing and packaging process. High tendency of torn glove remaining in food or products due to white or light flesh-coloured glove is not easy to be detected by naked eyes. In this paper, iron oxide nanoparticles (IONs) selected as additive for NBR to improve its detectability by mean of magnetic properties. IONs synthesized via precipitation method and compounded with NBR latex before casting on petri dish. The properties of IONs were investigated by X-ray Diffractometry (XRD), Transmission Electron Microscope (TEM), Raman Spectroscopy and Vibrating Sample Magnetometer (VSM). Meanwhile NBR/IONs composites were studied by Thermogravimetry Analysis (TGA), Differential Scanning Calorimetry (DSC) and Vibrating Sample Magnetometer (VSM). It observed that, synthesized IONs shows of 25.28 nm crystallite with 25.86 nm semipherical (changed as) shape. Meanwhile, Magnetite and maghemite phase are found in range of 670 cm{sup −1} and 700 cm{sup −1} respectively, which it contributes magnetization saturation of 73.96 emu/g at 10,000 G by VSM. Thermal stability and magnetic properties were increased with incorporating IONs into NBR latex up to 20 phr. NBR/IONs 5 phr has the optimum thermal stability, lowest glass transition temperature (−14.83 °C) and acceptable range of magnetization saturation (3.83 emu/g at 10,000 G) to form NBR gloves with magnetic detectability. - Highlights: • We synthesized IONs with high magnetization saturation (M{sub s}). • High M{sub s} of IONs were incorporated into NBR latex in order to induce magnetic properties in the NBR composite. • Introduction of IONs into NBR latex would improve thermal properties. • The produced NBR/IONs 5 phr composite exceeded the minimum magnetic moment sensor of the detector. • They have high

  8. Theoretical Kinetics Analysis for Ḣ Atom Addition to 1,3-Butadiene and Related Reactions on the Ċ4H7Potential Energy Surface.

    Science.gov (United States)

    Li, Yang; Klippenstein, Stephen J; Zhou, Chong-Wen; Curran, Henry J

    2017-10-12

    The oxidation chemistry of the simplest conjugated hydrocarbon, 1,3-butadiene, can provide a first step in understanding the role of polyunsaturated hydrocarbons in combustion and, in particular, an understanding of their contribution toward soot formation. On the basis of our previous work on propene and the butene isomers (1-, 2-, and isobutene), it was found that the reaction kinetics of Ḣ-atom addition to the C═C double bond plays a significant role in fuel consumption kinetics and influences the predictions of high-temperature ignition delay times, product species concentrations, and flame speed measurements. In this study, the rate constants and thermodynamic properties for Ḣ-atom addition to 1,3-butadiene and related reactions on the Ċ 4 H 7 potential energy surface have been calculated using two different series of quantum chemical methods and two different kinetic codes. Excellent agreement is obtained between the two different kinetics codes. The calculated results including zero-point energies, single-point energies, rate constants, barrier heights, and thermochemistry are systematically compared among the two quantum chemical methods. 1-Methylallyl (Ċ 4 H 7 1-3) and 3-buten-1-yl (Ċ 4 H 7 1-4) radicals and C 2 H 4 + Ċ 2 H 3 are found to be the most important channels and reactivity-promoting products, respectively. We calculated that terminal addition is dominant (>80%) compared to internal Ḣ-atom addition at all temperatures in the range 298-2000 K. However, this dominance decreases with increasing temperature. The calculated rate constants for the bimolecular reaction C 4 H 6 + Ḣ → products and C 2 H 4 + Ċ 2 H 3 → products are in excellent agreement with both experimental and theoretical results from the literature. For selected C 4 species, the calculated thermochemical values are also in good agreement with literature data. In addition, the rate constants for H atom abstraction by Ḣ atoms have also been calculated, and it is

  9. Cytotoxicity, genotoxicity, and mutagenicity of 1-chloro-2-hydroxy-3-butene and 1-chloro-3-buten-2-one, two alternative metabolites of 1,3-butadiene

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Xin-Jie; Zeng, Fang-Mao; An, Jing; Yu, Ying-Xin [Institute of Environmental Pollution and Health, School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444 (China); Zhang, Xin-Yu, E-mail: xyzhang999@shu.edu.cn [Institute of Environmental Pollution and Health, School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444 (China); Elfarra, Adnan A., E-mail: elfarra@svm.vetmed.wisc.edu [Department of Comparative Biosciences, University of Wisconsin-Madison, Madison, WI 53706 (United States); Molecular and Environmental Toxicology Center, University of Wisconsin-Madison, Madison, WI 53706 (United States)

    2013-08-15

    The cytotoxicity, genotoxicity, and mutagenicity of 1-chloro-2-hydroxy-3-butene (CHB), a known in vitro metabolite of the human carcinogen 1,3-butadiene, have not previously been investigated. Because CHB can be bioactivated by alcohol dehydrogenases to yield 1-chloro-3-buten-2-one (CBO), a bifunctional alkylating agent that caused globin-chain cross-links in erythrocytes, in the present study we investigated the cytotoxic and genotoxic potential of CHB and CBO in human normal hepatocyte L02 cells using the MTT assay, the relative cloning efficiency assay and the comet assay. We also investigated the mutagenic potential of these compounds with the Ames test using Salmonella strains TA1535 and TA1537. The results provide clear evidence for CHB and CBO being both cytotoxic and genotoxic with CBO being approximately 100-fold more potent than CHB. Interestingly, CHB generated both single-strand breaks and alkali-labile sites on DNA, whereas CBO produced only alkali-labile sites. CHB did not directly result in DNA breaks, whereas CBO was capable of directly generating breaks on DNA. Interestingly, both compounds did not induce DNA cross-links as examined by the comet assay. The Ames test results showed that CHB induced point mutation but not frameshift mutation, whereas the toxic effects of CBO made it difficult to reliably assess the mutagenic potential of CBO in the two strains. Collectively, the results suggest that CHB and CBO may play a role in the mutagenicity and carcinogenicity of 1,3-butadiene. - Highlights: • 1-Chloro-2-hydroxy-3-butene (CHB) is cytotoxic and genotoxic in human liver cells. • The CHB metabolite, 1-chloro-3-buten-2-one (CBO) is ∼ 100-fold more toxic than CHB. • CHB and CBO cause DNA alkali-labile sites, but only CBO directly causes DNA breaks. • CHB is mutagenic in the Ames test, but CBO is too toxic in the assay. • The results suggest a role for CHB in 1,3-butadiene genotoxicity and mutagenicity.

  10. The effect of the central donor in bis(benzimidazole)-based cobalt catalysts for the selective cis-1,4-polymerisation of butadiene.

    Science.gov (United States)

    Cariou, Renan; Chirinos, Juan J; Gibson, Vernon C; Jacobsen, Grant; Tomov, Atanas K; Britovsek, George J P; White, Andrew J P

    2010-10-14

    A series of bis(benzimidazole)-based cobalt(II) dichloride complexes containing a range of different central donors has been synthesized and characterized. The nature of the central donor affects the binding of the ligand to the cobalt centre and determines the coordination geometry of the metal complexes. All complexes have been shown to catalyse the polymerization of butadiene, in combination with MAO as the co-catalyst, to give cis-1,4-polybutadiene with high selectivity. The nature of the central donor has a marked influence on the polymerization activity of the catalysts, but does not affect the polymer microstructure. The addition of PPh(3) generally increases the polymerization activity of these cobalt catalysts and results in predominantly (60-70%) 1,2-vinyl-polybutadiene.

  11. Observations made during stretching, tearing and failure of NR (natural rubber) and SBR (styrene-butadiene rubber) loaded with various amounts of carbon black

    Energy Technology Data Exchange (ETDEWEB)

    Goldberg, A.; Lesuer, D.R.; Patt, J.

    1988-02-01

    In order to effectively utilize fractography as an aid in identifying the influence of material and service (or test) parameters on material properties, one must first understand the origin of the morphological features developed during the tearing and fracturing of these elastomers. At our laboratory, we have made extensive fractographic studies while evaluating the effects of material formulations, temperature, and loading rates on the loading response, tearing energy, induced damage, and tearing phenomena in SBR (Styrene Butadiene Rubber) containing different amounts of CB (Carbon Black) filler. We have also examined failures in tank track pads, as well as laboratory-tested samples cut from new track pads. In this paper we report on observations made during the actual stretching, tearing and failure of elastomeric samples pulled in tension at a constraint stroke-diplacement rate. 15 refs., 12 figs.

  12. Copolymerization of 1-hexene and 1-dodecene with 1,3-butadiene by a versatate/diisobutylaluminum hydride/t-butyl chloride catalyst system

    Directory of Open Access Journals (Sweden)

    Gustavo Monteiro da Silva

    2014-01-01

    Full Text Available The aim of this study was to incorporate an alpha-olefin (1-hexene or 1-dodecene in a high cis polybutadiene chain, using a neodymium versatate/diisobutylaluminum hydride/t-butyl chloride catalyst system. The influence of alpha-olefin on polymerization reaction and polymer characteristics, using different weight ratios of butadiene/α-olefin, was evaluated. The copolymers were characterized by SEC, FTIR, NMR, TGA and viscosimetric analysis. The thermal stability of the polymer tended to increase with incorporation of alpha-olefins, while its microstructure was not affected. The weight average molecular mass (Mw tended to increase and the polymerization conversion tended to decrease with increasing alpha-olefins content. The copolymers showed a lower intrinsic viscosity than for the homopolymer. The results indicated that the alpha-olefins were incorporated in the polybutadiene chain.

  13. Effect of carbon black composition with sludge palm oil on the curing characteristic and mechanical properties of natural rubber/styrene butadiene rubber compound

    Science.gov (United States)

    Mohamed, R.; Nurazzi, N. Mohd; Huzaifah, M.

    2017-07-01

    This study was conducted to investigate the possibility of utilizing sludge palm oil (SPO) as processing oil, with various amount of carbon black as its reinforcing filler, and its effects on the curing characteristics and mechanical properties of natural rubber/styrene butadiene rubber (NR/SBR) compound. Rubber compound with fixed 15 pphr of SPO loading, and different carbon black loading from 20 to 50 pphr, was prepared using two roll mills. The cure characteristics and mechanical tests that have been conducted are the scorch and cure time analysis, tensile strength and tear strength. Scorch time (ts5) and cure time (t90) of the compound increases with the increasing carbon black loading. The mechanical properties of NR/SBR compound viz. the tensile strength, modulus at 300% strain and tear strength were also improved by the increasing carbon black loading.

  14. Effect of porosity and environment on the mechanical behavior of acrylic bone cement modified with acrylonitrile-butadiene-styrene particles: part II. Fatigue crack propagation.

    Science.gov (United States)

    Vila, M M; Ginebra, M P; Gil, F J; Planell, J A

    1999-01-01

    The aim of this study was to investigate the effect of adding an elastomeric second phase, acrylonitrile-butadiene-styrene, on the fatigue crack propagation behavior of poly(methyl methacrylate) bone cement. Moreover, the influence of porosity and environmental conditions was studied. When comparing the plain cement to the modified cement, a decrease in the crack propagation rate was observed at between 1 and 2 orders of magnitude. The storage in a physiological environment (saline solution at 37 degrees C) also caused a decrease in the crack propagation rate of about 2 orders of magnitude for the plain and modified cement prepared in air or under a vacuum. Porosity did not have any noticeable effect on the fatigue crack propagation behavior of the cement.

  15. Effect of porosity and environment on the mechanical behavior of acrylic bone cement modified with acrylonitrile-butadiene-styrene particles: I. Fracture toughness.

    Science.gov (United States)

    Vila, M M; Ginebra, M P; Gil, F J; Planell, J A

    1999-01-01

    The elastomeric copolymer acrylonitrile-butadiene-styrene (ABS) was added to a conventional acrylic bone cement matrix. The results obtained show that although strength and stiffness decreased with an increasing second phase volume fraction, ductility and toughness both increased. The crack propagation became stable for specimens containing over a 5% volume fraction of the second phase. The fracture toughness increased up to 60% when the amount of ABS reached 20% (v/v). For larger amounts linear elastic fracture mechanics techniques could not be used properly. The effects of porosity and environmental conditions on the mechanical behavior were also studied. The mechanisms that control the fracture process were investigated by means of scanning electron microscopy.

  16. Synchrotron-based FTIR microspectroscopy for the mapping of photo-oxidation and additives in acrylonitrile-butadiene-styrene model samples and historical objects.

    Science.gov (United States)

    Saviello, Daniela; Pouyet, Emeline; Toniolo, Lucia; Cotte, Marine; Nevin, Austin

    2014-09-16

    Synchrotron-based Fourier transform infrared micro-spectroscopy (SR-μFTIR) was used to map photo-oxidative degradation of acrylonitrile-butadiene-styrene (ABS) and to investigate the presence and the migration of additives in historical samples from important Italian design objects. High resolution (3×3 μm(2)) molecular maps were obtained by FTIR microspectroscopy in transmission mode, using a new method for the preparation of polymer thin sections. The depth of photo-oxidation in samples was evaluated and accompanied by the formation of ketones, aldehydes, esters, and unsaturated carbonyl compounds. This study demonstrates selective surface oxidation and a probable passivation of material against further degradation. In polymer fragments from design objects made of ABS from the 1960s, UV-stabilizers were detected and mapped, and microscopic inclusions of proteinaceous material were identified and mapped for the first time. Copyright © 2014 Elsevier B.V. All rights reserved.

  17. The individual and cumulative effect of brominated flame retardant and polyvinylchloride (PVC) on thermal degradation of acrylonitrile-butadiene-styrene (ABS) copolymer.

    Science.gov (United States)

    Brebu, Mihai; Bhaskar, Thallada; Murai, Kazuya; Muto, Akinori; Sakata, Yusaku; Uddin, Md Azhar

    2004-08-01

    Acrylonitrile-butadiene-styrene (ABS) copolymers without and with a polybrominated epoxy type flame retardant were thermally degraded at 450 degrees C alone (10 g) and mixed with polyvinylchloride (PVC) (8 g/2 g). Gaseous and liquid products of degradation were analysed by various gas chromatographic methods (GC with TCD, FID, AED, MSD) in order to determine the individual and cumulative effect of bromine and chlorine on the quality and quantity of degradation compounds. It was found that nitrogen, chlorine, bromine and oxygen are present as organic compounds in liquid products, their quantity depends on the pyrolysed polymer or polymer mixture. Bromophenol and dibromophenols were the main brominated compounds that come from the flame retardant. 1-Chloroethylbenzene was the main chlorine compound observed in liquid products. It was also determined that interactions appear at high temperatures during decomposition between the flame retardant, PVC and the ABS copolymer.

  18. Principais aspectos da polimerização do 1,3-butadieno Principles aspects of butadiene 1,3 polymerization

    Directory of Open Access Journals (Sweden)

    Denise S. S. Nunes

    2005-11-01

    Full Text Available Atualmente, há uma grande demanda pelo polibutadieno com alto teor de unidades 1,4-cis, devido às suas excelentes propriedades físicas, tais como alta resistência à abrasão, baixo desenvolvimento de calor, baixa resistência ao rolamento, maior resistência à tensão, alta resistência à fadiga, baixa histerese e alta resistência à fratura. Tais características fazem com que esse elastômero seja cada vez mais utilizado na indústria pneumática. Assim, este trabalho apresenta uma breve revisão sobre a polimerização do 1,3-butadieno com diferentes sistemas catalíticos, sendo os sistemas à base de lantanídeos o principal foco desta revisão, pois esses sistemas são os mais estereoespecíficos para a polimerização 1,4-cis do butadieno.Nowadays, there is a great demand for polybutadiene with high contents of cis groups owing to its excellent physical properties, such as high abrasion resistance and low heat build up. These characteristics make this elastomer one of the most used in pneumatic industry. Thus, this paper presents a brief review about the 1,3-butadiene polymerization by different catalysts systems, with the systems based on lanthanides being the main focus, as they are the most stereospecific for cis-1,4 polymerization of butadiene.

  19. Reaction of C5(CH3)5Hf(2,3-dimethyl-1,3-butadiene)Cl with Acetylene : Formation of an Asymmetric, Disubstituted 1,3-Dihafnacyclobutane

    NARCIS (Netherlands)

    Hessen, Bart; Bolhuis, Fré van; Teuben, Jan H.

    Cp*Hf(2,3-dimethyl-1,3-butadiene)Cl (Cp* = η5-C5Me5) reacts with 1 mol of acetylene to form a disubstituted 1,3-dihafnacyclobutane complex, {Cp*Hf(Cl)[μCHCHCH2C(Me)=C(Me)CH2]}2, which was characterized by X-ray analysis (triclinic space group P1, a = 8.446 (7) Å, b = 10.518 (2) Å, c = 10.792 (1) Å,

  20. Volume shrinkage and rheological studies of epoxidised and unepoxidised poly(styrene-block-butadiene-block-styrene) triblock copolymer modified epoxy resin-diamino diphenyl methane nanostructured blend systems.

    Science.gov (United States)

    George, Sajeev Martin; Puglia, Debora; Kenny, Josè M; Parameswaranpillai, Jyotishkumar; Vijayan P, Poornima; Pionteck, Jűrgen; Thomas, Sabu

    2015-05-21

    Styrene-block-butadiene-block-styrene (SBS) copolymers epoxidised at different epoxidation degrees were used as modifiers for diglycidyl ether of the bisphenol A-diamino diphenyl methane (DGEBA-DDM) system. Epoxy systems containing modified epoxidised styrene-block-butadiene-block-styrene (eSBS) triblock copolymer with compositions ranging from 0 to 30 wt% were prepared and the curing reaction was monitored in situ using rheometry and pressure-volume-temperature (PVT) analysis. By controlling the mole percent of epoxidation, we could generate vesicles, worm-like micelles and core-shell nanodomains. At the highest mole percent of epoxidation, the fraction of the epoxy miscible component in the triblock copolymer (epoxidised polybutadiene (PB)) was maximum. This gave rise to core-shell nanodomains having a size of 10-15 nm, in which the incompatible polystyrene (PS) becomes the core, the unepoxidised PB becomes the shell and the epoxidised PB interpenetrates with the epoxy phase. On the other hand, the low level of epoxidation gave rise to bigger domains having a size of ∼1 μm and the intermediate epoxidation level resulted in a worm-like structure. This investigation specifically focused on the importance of cure rheology on nanostructure formation, using rheometry. The reaction induced phase separation of the PS phase in the epoxy matrix was carefully explored through rheological measurements. PVT measurements during curing were carried out to understand the volume shrinkage of the blend, confirming that shrinkage behaviour is related to the block copolymer phase separation process during curing. The volume shrinkage was found to be maximum in the case of blends with unmodified SBS, where a heterogeneous morphology was observed, while a decrease in the shrinkage was evidenced in the case of SBS epoxidation. It could be explained by two effects: (1) solubility of the epoxidised block copolymer in the DGEBA leads to the formation of nanoscopic domains upon

  1. Kinetic and Mechanistic Studies for the Gas-phase Reaction of Ozone with 2, 3-Dimethyl-2-Butene and 1, 3-Butadiene

    Directory of Open Access Journals (Sweden)

    Ismael Abdulsatar AL Mulla

    2017-09-01

    Full Text Available The reactions of ozone with 2,3-Dimethyl-2-Butene (CH32C=C(CH32 and 1,3-Butadiene CH2=CHCH=CH2 have been investigated under atmospheric conditions at 298±3K in air using both relative and absolute rate techniques, and the measured rate coefficients are found to be in good agreement in both techniques used. The obtained results show the addition of ozone to the double bond in these compounds and how it acts as function of the methyl group substituent situated on the double bond. The yields of all the main products have been determined using FTIR and GC-FID and the product studies of these reactions establish a very good idea for the decomposition pathways for the primary formed compounds (ozonides and give a good information for the effect of the methyl group on the degradation pathways. The results have been discussed from the view point of their importance in the atmospheric oxidation of these pollutants.

  2. The effect of multifunctional monomers/oligomers Additives on electron beam radiation crosslinking of poly (styrene-block-isoprene/butadiene-block-styrene) (SIBS)

    Science.gov (United States)

    Wu, Jinping; Soucek, Mark D.

    2016-02-01

    The effect of multifunctional monomers or oligomers (MFM/O) additives on electron beam (E-beam) radiation induced crosslinking of poly (styrene-block-isoprene/butadiene-block-styrene) (SIBS) was studied. Ten types of MFM/O were investigated, including trimethylolpropane trimethacrylate (TMPTMA), trimethylolpropane triacrylate (TMPTA), triallyl cyanurate (TAC), polybutadiene diacrylate (PB-diacrylate), ethylene glycol dimethylacrylate (EGDMA), butylene glycol dimethacrylate (BGDMA), 1,2-polybutadiene. The effects of MFM/O concentration and E-beam radiation dose on properties of SIBS were studied including tensile strength, elongation-at-break, modulus, gel content, equilibrium swelling and crosslink density. TMPTA significantly improved the tensile modulus and crosslink density of SIBS. SIBS with TMPTMA and TMTPMA with inhibitor showed a 50% increase in tensile strength. The solubility of MFM/O in SIBS was also investigated by a selective swelling method. The MFM/O were found to be soluble in both phases of SIBS. The viscosity of SIBS with methacrylate type MFM/O was stable at 200 °C.

  3. Process Window for Direct Recycling of Acrylonitrile-Butadiene-Styrene and High-Impact Polystyrene from Electrical and Electronic Equipment Waste.

    Science.gov (United States)

    Vazquez, Yamila V; Barbosa, Silvia E

    2017-01-01

    The aim of this paper is to assess recycling process window of ABS (Acrylonitrile-Butadiene-Styrene) and HIPS (High impact Polystyrene) from WEEE (waste from electrical and electronic equipment) through a final properties/structure screening study on their blends. Main motivation is to evaluate which amount of one plastic WEEE can be included into the other at least keeping their properties. In this sense, a wider margin of error during sorting could be admitted to obtain recycling materials with similar technological application of recycled ABS and HIPS by themselves. Results are discussed in terms of final blend structure, focusing in the interaction, within blends, of copolymers phases and fillers presents in WEEE. The comparative analysis of mechanical performance and morphology of HIPS/ABS blends indicates that the addition of 50wt% HIPS to ABS even improves 50% the elongation at break maintaining the strength. On the opposite, HIPS maintains its properties with 20wt% of ABS added. This study allows enlarging composition process window of recycling plastic WEEE for similar applications. This could be a sustainable way to improve benefit of e-scrap with low costs and easy processability. In consequence, social interest in the recycling of this kind of plastic scrap could be encourage from either ecological or economical points of view. Copyright © 2016 Elsevier Ltd. All rights reserved.

  4. Heat shrinkable behavior, physico-mechanical and structure properties of electron beam cross-linked blends of high-density polyethylene with acrylonitrile-butadiene rubber

    Science.gov (United States)

    Reinholds, Ingars; Kalkis, Valdis; Merijs-Meri, Remo; Zicans, Janis; Grigalovica, Agnese

    2016-03-01

    In this study, heat-shrinkable composites of electron beam irradiated high-density polyethylene (HDPE) composites with acrylonitrile-butadiene rubber (NBR) were investigated. HDPE/NBR blends at a ratio of components 100/0, 90/10, 80/20, 50/50 and 20/80 wt% were prepared using a two-roll mill. The compression molded films were irradiated high-energy (5 MeV) accelerated electrons up to irradiation absorbed doses of 100-300 kGy. The effect of electron beam induced cross-linking was evaluated by the changes of mechanical properties, gel content and by the differences of thermal properties, detected by differential scanning calorimetry. The thermo-shrinkage forces were determined as the kinetics of thermorelaxation and the residual shrinkage stresses of previously oriented (stretched up to 100% at above melting temperature of HDPE and followed by cooling to room temperature) specimens of irradiated HDPE/NBR blends under isometric heating-cooling mode. The compatibility between the both components was enhanced due to the formation of cross-linked sites at amorphous interphase. The results showed increase of mechanical stiffness of composites with increase of irradiation dose. The values of gel fraction compared to thermorelaxation stresses increased with the growth of irradiation dose level, as a result of formation cross-linked sites in amorphous PP/NBR interphase.

  5. Adhesion properties of styrene-butadiene rubber (SBR/Standard Malaysian Rubber (SMR L-based adhesives in the presence of phenol formaldehyde resin

    Directory of Open Access Journals (Sweden)

    2007-10-01

    Full Text Available The adhesion properties, i. e. viscosity, tack and peel strength of styrene-butadiene rubber (SBR/Standard Malaysian Rubber (SMR L-based pressure-sensitive adhesive was studied using phenol formaldehyde resin as the tackifying resin. Toluene was used as the solvent throughout the experiment. SBR composition in SBR/SMR L blend used was 0, 20, 40, 60, 80, 100%. Three different resin loadings, i. e. 40, 80 and 120 parts per hundred parts of rubber (phr were used in the adhesive formulation. The viscosity of adhesive was determined by a HAAKE Rotary Viscometer whereas loop tack and peel strength of paper/polyethylene terephthalate (PET film were measured using a Lloyd Adhesion Tester operating at 30 cm/min. Results indicate that the viscosity of adhesive decreases with increasing % SBR whereas loop tack passes through a maximum value at 20% SBR for all resin loadings. Except for the control sample (without resin, the peel strength shows a maximum value at 60% SBR for the three modes of peel tests. For a fixed % SBR, adhesive sample containing 40 phr phenol formaldehyde resin always exhibits the highest loop tack and peel strength, an observation which is associated to the optimum wettability of adhesive on the substrate.

  6. Iminopyridine-Based Cobalt(II and Nickel(II Complexes: Synthesis, Characterization, and Their Catalytic Behaviors for 1,3-Butadiene Polymerization

    Directory of Open Access Journals (Sweden)

    Quanquan Dai

    2016-01-01

    Full Text Available A series of iminopyridine ligated Co(II (1a–7a and Ni(II (1b–7b complexes were synthesized. The structures of complexes 3a, 4a, 5a, 7a, 5b, and 6b were determined by X-ray crystallographic analyses. Complex 3a formed a chloro-bridged dimer, whereas 4a, 5a, and 7a, having a substituent (4a, 5a: CH3; 7a: Br at the 6-position of pyridine, producing the solid structures with a single ligand coordinated to the central metal. The nickel atom in complex 5b features distorted trigonal-bipyramidal geometry with one THF molecule ligating to the metal center. All the complexes activated by ethylaluminum sesquichloride (EASC were evaluated in 1,3-butadiene polymerization. The catalytic activity and selectivity were significantly influenced by the ligand structure and central metal. Comparing with the nickel complexes, the cobalt complexes exhibited higher catalytic activity and cis-1,4-selectivity. For both the cobalt and nickel complexes, the aldimine-based complexes showed higher catalyst activity than their ketimine counterparts.

  7. Effect of polypropylene maleic anhydride (PPMAH) on mechanical and morphological properties of polypropylene (PP)/recycled acrylonitrile butadiene rubber (NBRr)/empty fruit bunch (EFB) composites

    Science.gov (United States)

    Othman, Nurul Syazwani; Santiagoo, Ragunathan; Abdillahi, Khalid Mohamed; Ismail, Hanafi

    2017-07-01

    The fabrication of polypropylene (PP)/ recycled acrylonitrile butadiene rubber (NBRr)/ empty fruit bunch (EFB) composites were investigated. The effects of polypropylene maleic anhydride (PPMAH) as a compatibilizer on the mechanical and morphological properties of PP/NBRr/EFB composites were studied. Composites were prepared through melt mixing using heated two roll mill at 180 °C for 9 minutes and rotor speed of 15 rpm. NBRr loading were varied from 0 to 60 phr and PPMAH was fixed for 5 phr. The composites were moulded into a 1 mm thin sheet using hot press machine and then cut into dumbbell shape. The mechanical and morphological properties of composites were examined using universal tensile machine (UTM) and scanning electron microscope (SEM), respectively. Tensile strength and Young's modulus of PP/NBRr/EFB composites decreased with increasing NBRr loading, whilst increasing the elongation at break. However, PPMAH compatibilized composites have resulted 27% to 40% and 25% to 42% higher tensile strength and Young's modulus, respectively, higher compared to uncompatibilized composites. This was due to the better adhesion between PP/NBRr matrices and EFB filler with the presence of maleic anhydride moieties. From the morphological study, the micrograph of PPMAH compatibilized composites has proved the well bonded and good attachments of EFB filler with PP/NBRr matrices which results better tensile strength to the PP/NBRr/EFB composites.

  8. Shape Memory Polymer Composites of Poly(styrene-b-butadiene-b-styrene Copolymer/Liner Low Density Polyethylene/Fe3O4 Nanoparticles for Remote Activation

    Directory of Open Access Journals (Sweden)

    Yongkun Wang

    2016-11-01

    Full Text Available Magnetically sensitive shape memory poly(styrene-b-butadiene-b-styrene copolymer (SBS/liner low density polyethylene (LLDPE composites filled with various contents of Fe3O4 nanoparticles were prepared. The influence of the Fe3O4 nanoparticles content on the thermal properties, mechanical properties, fracture morphology, magnetic behavior, and shape memory effect of SBS/LLDPE/Fe3O4 composites was systematically studied in this paper. The results indicated that homogeneously dispersed Fe3O4 nanoparticles ensured the uniform heat generation and transfer in the alternating magnetic field, and endowed the SBS/LLDPE/Fe3O4 composites with an excellent magnetically responsive shape memory effect. When the shape memory composites were in the alternating magnetic field (f = 60 kHz, H = 21.21 kA·m−1, the best shape recovery ratio reached 99%, the shape retention ratio reached 99.4%, and the shape recovery speed increased significantly with the increment of Fe3O4 nanoparticles. It is anticipated that tagging products with this novel shape memory composite is helpful for the purpose of an intravascular delivery system in Micro-Electro-Mechanical System (MEMS devices.

  9. Synthesis and Molecular Structures of Two [1,4-bis(3-pyridyl-2,3-diazo-1,3-butadiene]-dichloro-Zn(II Coordination Polymers

    Directory of Open Access Journals (Sweden)

    Hsin-Ta Wang

    2006-08-01

    Full Text Available Two novel coordination polymers with 3D metal-organic frameworks (MOFs have been synthesized by reacting 1,4-bis(3-pyridyl-2,3-diazo-1,3-butadiene (L with zinc dichloride. Both compounds have the same repeating unit consisting of a distorted tetrahedral Zn(II center coordinated by two chlorides and two pyridyl nitrogen atoms of two bridging bismonodentate L ligands, however, different structural conformations have been found, one forming a helical chain and the other producing a square-wave chain. The intermolecular C−H···Cl hydrogen bonds in 1 and 2 play important roles in the formation of three-dimensional coordination polymers. Compound 1 crystallized in an orthorhombic space group Pna21 with a = 7.9652(3, b = 21.4716(7, c = 8.2491(3Å, V = 1410.81(9 Å 3 and Z = 4. Compound 2 crystallized in a monoclinic space group P21/n with a = 9.1752(3, b = 14.5976(4, c = 10.3666(3 Å , β = 98.231(2°, V = 1374.16(7 Å 3 and Z = 4.

  10. Utilizing carbon dioxide as a reaction medium to mitigate production of polycyclic aromatic hydrocarbons from the thermal decomposition of styrene butadiene rubber.

    Science.gov (United States)

    Kwon, Eilhann E; Yi, Haakrho; Castaldi, Marco J

    2012-10-02

    The CO(2) cofeed impact on the pyrolysis of styrene butadiene rubber (SBR) was investigated using thermogravimetric analysis (TGA) coupled to online gas chromatography/mass spectroscopy (GC/MS). The direct comparison of the chemical species evolved from the thermal degradation of SBR in N(2) and CO(2) led to a preliminary mechanistic understanding of the formation and relationship of light hydrocarbons (C(1-4)), aromatic derivatives, and polycyclic aromatic hydrocarbons (PAHs), clarifying the role of CO(2) in the thermal degradation of SBR. The identification and quantification of over 50 major and minor chemical species from hydrogen and benzo[ghi]perylene were carried out experimentally in the temperature regime between 300 and 500 °C in N(2) and CO(2). The significant amounts of benzene derivatives from the direct bond dissociation of the backbone of SBR, induced by thermal degradation, provided favorable conditions for PAHs by the gas-phase addition reaction at a relatively low temperature compared to that with conventional fuels such as coal and petroleum-derived fuels. However, the formation of PAHs in a CO(2) atmosphere was decreased considerably (i.e., ∼50%) by the enhanced thermal cracking behavior, and the ultimate fates of these species were determined by different pathways in CO(2) and N(2) atmospheres. Consequently, this work has provided a new approach to mitigate PAHs by utilizing CO(2) as a reaction medium in thermochemical processes.

  11. Characterization of free volume during vulcanization of styrene butadiene rubber by means of positron annihilation lifetime spectroscopy and dynamic mechanical test.

    Science.gov (United States)

    Marzocca, A J; Cerveny, S; Salgueiro, W; Somoza, A; Gonzalez, L

    2002-02-01

    An experimental investigation was performed to study the effect on the free volume of the advance of the cross-linking reaction in a copolymer of styrene butadiene rubber by sulfur vulcanization. The dynamic modulus and loss tangent were evaluated over samples cured for different times at 433 K by dynamic mechanical tests over a range of frequencies between 5 and 80 Hz at temperatures between 200 and 300 K. Using the William-Landel-Ferry relationship, master curves were obtained at a reference temperature of 298 K and the coefficients c(0)(1) and c(0)(2) were evaluated. From these parameters the dependence of the free volume on the cure time is obtained. Positron annihilation lifetime spectroscopy was also used to estimate the size and number density of free volume sites in the material. The spectra were analyzed in terms of continuous distributions of free volume size. The results suggest an increase of the lower free volume size when cross linking takes place. Both techniques give similar results for the dependence of free volume on the time of cure of the polymer.

  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. The use of styrene-butadiene rubber waste as a potential filler in nitrile rubber: order of addition and size of waste particles

    Directory of Open Access Journals (Sweden)

    D. A. Baeta

    2009-03-01

    Full Text Available Styrene-butadiene rubber (SBR has large applications in the shoe industry, especially as expanded sheets used to produce insoles and inner soles. According to TG analysis, the rubber content in SBR residues (SBR-r was found to be around 26-wt%. Based on that data, a cost-effective technique for the reuse of SBR-r in Nitrile rubber (NBR was developed. Later, the effect of SBR-r on the cure behavior, mechanical performance, swelling, and crosslink density of reused rubber was investigated, with more emphasis placed on the effect of both particle size and loading of waste filler. Cure characteristics such as optimum cure time and scorch time were then reduced by the increasing amount of SBR-r filler. Owing to the reinforced nature of the largest particle size SBR-r, the best results for the mechanical properties of NBR were those in which SBR-r was added at the end of the cure process. The study has thus shown that SBR residue (SBR-r can be used as an economical alternative filler in NBR.

  14. Water soluble styrene butadiene rubber and sodium carboxyl methyl cellulose binder for ZnFe2O4 anode electrodes in lithium ion batteries

    Science.gov (United States)

    Zhang, Rongyu; Yang, Xu; Zhang, Dong; Qiu, Hailong; Fu, Qiang; Na, Hui; Guo, Zhendong; Du, Fei; Chen, Gang; Wei, Yingjin

    2015-07-01

    ZnFe2O4 nano particles as an anode material for lithium ion batteries are prepared by the glycine-nitrate combustion method. The mixture of styrene butadiene rubber and sodium carboxyl methyl cellulose (SBR/CMC) with the weight ratio of 1:1 is used as the binder for ZnFe2O4 electrode. Compared with the conventional polyvinylidene-fluoride (PVDF) binder, the SBR/CMC binder is much cheaper and environment benign. More significantly, this water soluble binder significantly improves the rate capability and cycle stability of ZnFe2O4. A discharge capacity of 873.8 mAh g-1 is obtained after 100 cycles at the 0.1C rate, with a very little capacity fading rate of 0.06% per cycle. Studies show that the SBR/CMC binder enhances the adhesion of the electrode film to the current collector, and constructs an effective three-dimensional network for electrons transport. In addition, the SBR/CMC binder helps to form a uniform SEI film thus prohibiting the formation of lithium dendrite. Electrochemical impedance spectroscopy shows that the SBR/CMC binder lowers the ohmic resistance of the electrode, depresses the formation of SEI film and facilitates the charge transfer reactions at the electrode/electrolyte interface. These advantages highlight the potential applications of SBR/CMC binder in lithium ion batteries.

  15. Mechanical and optical effects of elastomer interaction in polypropylene modification: Ethylene-propylene rubber, poly-(ethylene-co-octene and styrene-butadiene elastomers

    Directory of Open Access Journals (Sweden)

    M. Gahleitner

    2012-09-01

    Full Text Available The interaction between binary combinations of three different elastomer classes commonly applied in impact modification of isotactic polypropylene (iPP was studied. Blends based on a homogeneous ethylene-propylene (EP random copolymer (EP-RACO and a heterophasic EP impact copolymer comprising ethylene-propylene rubber (EPR with different external elastomer types, one homogeneous ethylene-1-octene copolymer (EOC, and two hydrogenated styrenebutadiene-styrene triblock copolymers (SEBS with different styrene content, were prepared. The phase morphology, mobility as a function of temperature, mechanical and optical properties were studied. Special effects could be achieved for the combination of two different elastomer types. The results clearly demonstrate the possibility to achieve attractive property combinations in ternary systems consisting of a crystalline PP matrix and two different types of elastomer, EPR or EOC on the one hand and SEBS on the other hand. A combination of density matching and compatibilization effects allows reaching good low temperature impact strength together with a transparency close to matrix level when selecting a butadiene-rich SEBS type.

  16. Effects of single and repeated exposures to thermo-oxidative degradation products of poly(acrylonitrile-butadiene-styrene) (ABS) on rat lung, liver, kidney, and brain.

    Science.gov (United States)

    Zitting, A; Savolainen, H

    1980-12-01

    Male Wistar rats were exposed to thermo-oxidative degradation products of heated poly(acrylonitrile-butadiene-styrene) (ABS). The exposures were conducted once, three times or ten times (5 nights/week, 6 h/night) in the nighttime. The degradation products included styrene, various nitriles, aldehydes, acids, and a significant aerosol fraction. The oxygen concentration in the exposure chamber was constantly above 20%. The shortest exposures caused a significant reduction of the 0-deethylation activity in lung and kidney but not in liver, as well as a decrease in tissue reduced glutathione concentration in liver and kidney but not in lung. These effects well-nigh disappeared during the two-week exposure. In these rats the cerebral glutathione was below the control range. Superoxide dismutase activity increased in liver and brain during the three-day exposure. In liver the activity reached the control value after the two-week exposure but the cerebral activity was significantly lower than in controls. The complex mixture of noxious compounds in the ABS fumes does not readily allow identification of causative agents. Nitrile-dependent histotoxic, peroxidative and reactive metabolite mediated mechanisms may be involved.

  17. Comprehensive analysis of the toxic and refractory pollutants in acrylonitrile-butadiene-styrene resin manufacturing wastewater by gas chromatography spectrometry with a mass or flame ionization detector.

    Science.gov (United States)

    Lai, Bo; Zhou, Yuexi; Yang, Ping; Wang, Ke

    2012-06-29

    Acrylonitrile-butadiene-styrene (ABS) resin manufacturing wastewater is a complicated, toxic and refractory industrial wastewater. Comprehensive and accurate analysis of the typical pollutants in ABS resin manufacturing wastewater is critical to develop cost-effective wastewater treatment technologies. In this paper, a comprehensively qualitative analysis combined with three complementary methods has been developed for the detection of typical pollutants in ABS resin manufacturing wastewater from three production sections, and thirty-seven compounds had been detected and further confirmed by this analysis method with standards. Simultaneous chromatographic separation and quantification of seven representative pollutants, including three mononuclear aromatics, three acrylonitrile dimers and one acrylonitrile derivative, were achieved by GC-FID system. The detection limits of this method for seven representative pollutants were in the range of 0.007-0.89 mg/L. The within-day and between-day precisions of this method were less than 6.5% (RSD, n=6). The recoveries of the representative pollutants reached 90-120%. The ABS resin manufacturing wastewater from E zone was successfully determined by this method, with two mononuclear aromatics and three acrylonitrile dimers accounting for 57.73% and 40.63% of the selected seven compounds, respectively. These results reveal that the removal of mononuclear aromatics and acrylonitrile dimers is a key to treat this wastewater. Crown Copyright © 2012. Published by Elsevier B.V. All rights reserved.

  18. One-step preparation of superhydrophobic acrylonitrile-butadiene-styrene copolymer coating for ultrafast separation of water-in-oil emulsions.

    Science.gov (United States)

    Deng, Wanshun; Long, Mengying; Zhou, Qiannan; Wen, Ni; Deng, Wenli

    2017-09-23

    Superhydrophobic membranes with opposite wettability toward water and oil are able to separate water-in-oil emulsions. By constructing porous and hierarchal-structured superhydrophobic coating on filter paper, we hope a quick separation process could be achieved due to the acceleration of both demulsification and penetration process. Here, superhydrophobic coatings were prepared by simply spraying environmental and cost-effective acrylonitrile-butadiene-styrene copolymer (ABS) colloid in dichloromethane onto filter paper. The morphologies and wettability of the obtained coatings were carefully studied. Moreover, the separation performances in dealing with various surfactant-stabilized water-in-oil emulsions (SSWOE) were also investigated to verify our hypothesis. The morphologies of the ABS coatings varied with its weight concentration in dichloromethane and they changed from porous and plain surface into porous and hierarchal-structured surface. Besides, the hydrophobicity of the above coatings varied form hydrophobic to superhydrophobic. Moreover, the resulted superhydrophobic membranes show great separation capability in separating various span 80-stabilized water-in-oil emulsions with oil filtrate purities larger than 99.90% and huge penetration fluxes whose maximum is over 13,000L/(m(2)h). Thus, we envision that such membrane can be a practical candidate in dealing with water-in-oil emulsions to obtain pure oils. Copyright © 2017. Published by Elsevier Inc.

  19. 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.

  20. 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

    2014-08-04

    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.

  1. 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.

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

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Tingting; Zhang, Jun, E-mail: zhangjun@njtech.edu.cn

    2016-12-01

    Highlights: • Surface hydrophilic modified ABS was prepared by melt blending with PETG. • O= C−O groups were enriched on the surface with increasing PETG content. • Hydrophilic property of the blends was enhanced with increasing PETG content. • Phase inversion behavior of the blends occurred around intermediate composition. • Tensile and flexural strength were enhanced with increasing PETG content. - Abstract: 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

  4. Mechanical Characterization of Hybrid Vesicles Based on Linear Poly(Dimethylsiloxane-b-Ethylene Oxide and Poly(Butadiene-b-Ethylene Oxide Block Copolymers

    Directory of Open Access Journals (Sweden)

    Jeffery Gaspard

    2016-03-01

    Full Text Available Poly(dimethylsiloxane-ethylene oxide (PDMS-PEO and poly(butadiene-b-ethylene oxide (PBd-PEO are two block copolymers which separately form vesicles with disparate membrane permeabilities and fluidities. Thus, hybrid vesicles formed from both PDMS-PEO and PBd-PEO may ultimately allow for systematic, application-specific tuning of vesicle membrane fluidity and permeability. However, given the relatively low strength previously noted for comb-type PDMS-PEO vesicles, the mechanical robustness of the resulting hybrid vesicles must first be confirmed. Toward this end, we have characterized the mechanical behavior of vesicles formed from mixtures of linear PDMS-PEO and linear PBd-PEO using micropipette aspiration. Tension versus strain plots of pure PDMS12-PEO46 vesicles revealed a non-linear response in the high tension regime, in contrast to the approximately linear response of pure PBd33-PEO20 vesicles. Remarkably, the area expansion modulus, critical tension, and cohesive energy density of PDMS12-PEO46 vesicles were each significantly greater than for PBd33-PEO20 vesicles, although critical strain was not significantly different between these vesicle types. PDMS12-PEO46/PBd33-PEO20 hybrid vesicles generally displayed graded responses in between that of the pure component vesicles. Thus, the PDMS12-PEO46/PBd33-PEO20 hybrid vesicles retained or exceeded the strength and toughness characteristic of pure PBd-PEO vesicles, indicating that future assessment of the membrane permeability and fluidity of these hybrid vesicles may be warranted.

  5. Comparative acute toxicity of leachates from plastic products made of polypropylene, polyethylene, PVC, acrylonitrile-butadiene-styrene, and epoxy to Daphnia magna.

    Science.gov (United States)

    Lithner, Delilah; Nordensvan, Ildikó; Dave, Göran

    2012-06-01

    The large global production of plastics and their presence everywhere in the society and the environment create a need for assessing chemical hazards and risks associated with plastic products. The aims of this study were to determine and compare the toxicity of leachates from plastic products made of five plastics types and to identify the class of compounds that is causing the toxicity. Selected plastic types were those with the largest global annual production, that is, polypropylene, polyethylene, and polyvinyl chloride (PVC), or those composed of hazardous monomers (e.g., PVC, acrylonitrile-butadiene-styrene [ABS], and epoxy). Altogether 26 plastic products were leached in deionized water (3 days at 50°C), and the water phases were tested for acute toxicity to Daphnia magna. Initial Toxicity Identification Evaluations (C18 filtration and EDTA addition) were performed on six leachates. For eleven leachates (42%) 48-h EC50s (i.e the concentration that causes effect in 50 percent of the test organisms) were below the highest test concentration, 250 g plastic/L. All leachates from plasticized PVC (5/5) and epoxy (5/5) products were toxic (48-h EC50s ranging from 2 to 235 g plastic/L). None of the leachates from polypropylene (5/5), ABS (5/5), and rigid PVC (1/1) products showed toxicity, but one of the five tested HDPE leachates was toxic (48-h EC50 17-24 g plastic/L). Toxicity Identification Evaluations indicated that mainly hydrophobic organics were causing the toxicity and that metals were the main cause for one leachate (metal release was also confirmed by chemical analysis). Toxic chemicals leached even during the short-term leaching in water, mainly from plasticized PVC and epoxy products.

  6. 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.

  7. Polymerization of 1,3-butadiene catalyzed by pincer cobalt(II) complexes derived from 2-(1-arylimino)-6-(pyrazol-1-yl)pyridine ligands

    KAUST Repository

    Gong, Dirong

    2013-08-01

    A new class of air stable and structurally well-defined cobalt complexes with unsymmetrical pincer type ligands ([2-(ArNCMe)-6-(Py)C5H 3N]CoCl2) (Ar = C6H5, Py = pyrazol-1-yl, 5a; Ar = 2,4,6-Me3C6H2, Py = pyrazol-1-yl, 5b; Ar = 2,6-iPr2C6H3, Py = pyrazol-1-yl, 5c; Ar = C6H5, Py = 3,5-Me 2pyrazol-1-yl, 5d; Ar = 2,4,6-Me3C6H 2, Py = 3,5-Me2pyrazol-1-yl, 5e; Ar = 2,6- iPr2C6H3, Py = 3,5-Me 2pyrazol-1-yl, 5f; Ar = 2,6-iPr2C 6H3, Py = 3,5-iPr2pyrazol-1-yl, 5g and [2-(OCMe)-6-(3,5-diphenylpyrazol-1-yl)C5H3N]CoCl 2 5h) were prepared and the molecular structures of 5a, 5c and 5f were determined by single crystal X-ray crystallography. Upon activation by methylaluminoxane (MAO) in toluene at room temperature, all complexes initiate polymerization of 1,3-butadiene (polymer yields: 65-99%), affording polybutadiene with excellent cis-1,4 regularity (97.5-98.7%). The polymer yields and properties in terms of molecular weight and distribution are well controlled by the substituents on iminoaryl rings and pyrazole rings. Selectivity switch from cis-1,4 to syndio-1,2 was also achievable by adding phosphine as microstructure regulator. © 2013 Elsevier B.V. All rights reserved.

  8. 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.

  9. Principais copolímeros elastoméricos à base de butadieno utilizados na indústria automobilística The most important butadiene based elastomers employed in the automotive industry

    Directory of Open Access Journals (Sweden)

    Tereza C. J. Rocha

    2007-12-01

    Full Text Available Copolímeros elastoméricos à base de butadieno são amplamente utilizados na indústria automobilística. Dentre esses destacam-se os copolímeros de butadieno-estireno (SBR e butadieno-acrilonitrila (NBR. O SBR apresenta maior importância comercial, devido a sua aplicação na produção de pneus. Quando SBR é utilizado juntamente com o homopolímero de butadieno BR-alto cis, excelentes propriedades são obtidas para sua aplicação na banda de rodagem de pneus. O copolímero elastomérico NBR é empregado em artefatos em que é necessária boa resistência a solventes orgânicos e a óleos. Nos últimos anos, as empresas automobilísticas e produtoras de pneumáticos vêm se preocupando com o meio-ambiente e, conseqüentemente, têm investido em novos processos de síntese, mais limpos, para a produção desses elastômeros. Assim, o objetivo deste artigo é apresentar uma revisão sobre dois importantes copolímeros elastoméricos à base de butadieno, SBR e NBR, abordando os processos de síntese, características principais, processamento e aplicações.Elastomer copolymers based on butadiene are widely applied in the automotive industry. Among those copolymers the most important ones are styrene-butadiene (SBR and nitrile-butadiene (NBR. SBR presents higher commercial interest, due to its application in the tire production. When SBR is mixed with high cis-1,4 polybutadiene, excellent properties are attained for application on the pneumatics treads. NBR can be used in a wide variety of application areas requiring oil, fuel, and chemical resistance. In the last years, the automotive and pneumatic industries have been increasingly concerned with environmental issues, and have invested in synthesis processes for elastomers that are less aggressive to the environment. Thus, the purpose of this article is to present a review on two important butadiene elastomer copolymers, SBR and NBR, with emphasis on the polymerization processes. The main

  10. Regio- and stereo-selective polymerization of 1,3-butadiene catalyzed by phosphorus–nitrogen PN3-pincer cobalt(ii) complexes

    KAUST Repository

    Gong, Dirong

    2016-11-11

    A new family of cobalt complexes (CoCl2-H, CoCl2-Me, CoCl2-iPr, CoBr2-H, CoBr2-Me, CoBr2-iPr, CoI2-H, CoI2-Me, and CoI2-iPr) supported by a PN3 ligand (6-(N,N′-di-t-butylphosphino)-2-pyrazol-yl-aminopyridine) have been prepared and fully characterized by FT-IR, elemental analysis, and X-ray analysis. The X-ray analysis reveals a trigonal bipyramidal conformation in the solid state for all representative complexes, CoCl2-H, CoBr2-H, CoBr2-iPr and CoI2-Me. The cobalt center is chelated by the PN3 ligand through the pyridinyl nitrogen, the pyrazol nitrogen and the phosphorus donor, with a long Co-P bond distance indicating a labile character. On activation with AlEt2Cl, Al2Et3Cl3, MAO, [Ph3C]+[B(C6F5)4]-/AliBu3 or AliBu3, cis-1,4 selective butadiene polymerization was achieved with up to 98.6% selectivity. The polymerization results show that the cis-1,4 selectivity is influenced by the steric hindrance, increasing with the bulkiness of the substituent groups (CoX2-iPr > CoX2-Me > CoX2-H) at the 3,5-positions of the pyrazole moiety, together with a slight decrease in activity. The activity changes in the order CoCl2L ≈ CoBr2L > CoI2L (for the same ligand L) when MAO is used as the activator, while the high level of cis-1,4 selectivity is maintained. It is possible to switch the selectivity from cis-1,4 to syndiotactic-1,2 by adding PPh3 © The Royal Society of Chemistry.

  11. Novel synthesis of magnesium hydroxide nanoparticles modified with organic phosphate and their effect on the flammability of acrylonitrile-butadiene styrene nanocomposites

    Energy Technology Data Exchange (ETDEWEB)

    Attia, Nour F., E-mail: drnour2005@yahoo.com [Fire Protection Laboratory, Chemistry Division, National Institute of Standards, 136, Giza 12211 (Egypt); Goda, Emad S.; Nour, M.A. [Fire Protection Laboratory, Chemistry Division, National Institute of Standards, 136, Giza 12211 (Egypt); Sabaa, M.W. [Chemistry Department, Faculty of Science, Cairo University, NahdetMisr Street, Giza 12613 (Egypt); Hassan, M.A., E-mail: Mohamed_a_hassan@hotmail.com [Fire Protection Laboratory, Chemistry Division, National Institute of Standards, 136, Giza 12211 (Egypt)

    2015-11-15

    New and facile method for the synthesis and modification of magnesium hydroxide nanoparticles has been developed. The organic phosphate was used to facilitate the synthesis and wrapping of magnesium hydroxide nanoparticles with organic phosphate shell. The size of the nanoparticles wrapped with phosphate has an average diameter range from 46 to 125 nm. The preparation method has governed the nanoparticles diameter based on reaction time. Thermal stability and morphological properties of the new nanoparticles coated phosphates were investigated. The developed magnesium hydroxide nanoparticles-organic phosphate achieved a very good compatibility when dispersed in acrylonitrile-butadiene styrene polymer (ABS) produced dispersed nanocomposites. The flammability and thermal properties of the new polymer nanocomposites were studied. The rate of burning of the nanocomposites was reduced to 9.8 mm/min compared to 15, 21.9 and 42.5 mm/min for polymer-conventional magnesium hydroxide composite, polymer-conventional magnesium hydroxide-organic phosphate composite and virgin polymer, respectively. The peak heat release rate (PHRR) and total heat release (THR) of the new nanocomposites were recorded as 243.4 kW/m{sup 2} and 19.2 MJ/m{sup 2}, respectively, achieved 71% reduction for PHRR and 55% for THR. The synergism between magnesium hydroxide nanoparticles and organic phosphates shell was also studied. The developed nanoparticles suppressed the emission of toxic gases. The different materials were characterized using thermal gravimetric analysis, fourier transform infrared spectroscopy, transmission electron microscopy. The flammability properties were evaluated using UL94 horizontal method and cone calorimeter. The dispersion of magnesium hydroxide nanoparticles-organic phosphate in ABS was studied using scanning electron microscope. - Highlights: • Novel and facile nanoparticles synthesis and modification have developed. • Magnesium hydroxide nanoparticles size has

  12. Complex phase separation in poly(acrylonitrile-butadiene-styrene)-modified epoxy/4,4'-diaminodiphenyl sulfone blends: generation of new micro- and nanosubstructures.

    Science.gov (United States)

    Jyotishkumar, P; Koetz, Joachim; Tiersch, Brigitte; Strehmel, Veronika; Ozdilek, Ceren; Moldenaers, Paula; Hässler, Rudiger; Thomas, Sabu

    2009-04-23

    The epoxy system containing diglycidyl ether of bisphenol A and 4,4'-diaminodiphenyl sulfone is modified with poly(acrylonitrile-butadiene-styrene) (ABS) to explore the effects of the ABS content on the phase morphology, mechanism of phase separation, and viscoelastic properties. The amount of ABS in the blends was 5, 10, 15, and 20 parts per hundred of epoxy resin (phr). Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) were employed to investigate the final morphology of ABS-modified epoxy blends. Scanning electron microscopic studies of 15 phr ABS-modified epoxy blends reveal a bicontinuous structure in which both epoxy and ABS are continuous, with substructures of the ABS phase dispersed in the continuous epoxy phase and substructures of the epoxy phase dispersed in the continuous ABS phase. TEM micrographs of 15 phr ABS-modified epoxy blends confirm the results observed by SEM. TEM micrographs reveal the existence of nanosubstructures of ABS in 20 phr ABS-modified epoxy blends. To the best of our knowledge, to date, nanosubstructures have never been reported in any epoxy/thermoplastic blends. The influence of the concentration of the thermoplastic on the generated morphology as analyzed by SEM and TEM was explained in detail. The evolution and mechanism of phase separation was investigated in detail by optical microscopy (OM) and small-angle laser light scattering (SALLS). At concentrations lower than 10 phr the system phase separates through nucleation and growth (NG). However, at higher concentrations, 15 and 20 phr, the blends phase separate through both NG and spinodal decomposition mechanisms. On the basis of OM and SALLS, we conclude that the phenomenon of complex substructure formation in dynamic asymmetric blends is due to the combined effect of hydrodynamics and viscoelasticity. Additionally, dynamic mechanical analysis was carried out to evaluate the viscoelastic behavior of the cross-linked epoxy/ABS blends. Finally

  13. In vivo doses of butadiene epoxides as estimated from in vitro enzyme kinetics by using cob(I)alamin and measured hemoglobin adducts: An inter-species extrapolation approach

    Energy Technology Data Exchange (ETDEWEB)

    Motwani, Hitesh V., E-mail: hitesh.motwani@mmk.su.se; Törnqvist, Margareta

    2014-12-15

    1,3-Butadiene (BD) is a rodent and human carcinogen. In the cancer tests, mice have been much more susceptible than rats with regard to BD-induced carcinogenicity. The species-differences are dependent on metabolic formation/disappearance of the genotoxic BD epoxy-metabolites that lead to variations in the respective in vivo doses, i.e. “area under the concentration-time curve” (AUC). Differences in AUC of the most gentoxic BD epoxy-metabolite, diepoxybutane (DEB), are considered important with regard to cancer susceptibility. The present work describes: the application of cob(I)alamin for accurate measurements of in vitro enzyme kinetic parameters associated with BD epoxy-metabolites in human, mouse and rat; the use of published data on hemoglobin (Hb) adduct levels of BD epoxides from BD exposure studies on the three species to calculate the corresponding AUCs in blood; and a parallelogram approach for extrapolation of AUC of DEB based on the in vitro metabolism studies and adduct data from in vivo measurements. The predicted value of AUC of DEB for humans from the parallelogram approach was 0.078 nM · h for 1 ppm · h of BD exposure compared to 0.023 nM · h/ppm · h as calculated from Hb adduct levels observed in occupational exposure. The corresponding values in nM · h/ppm · h were for mice 41 vs. 38 and for rats 1.26 vs. 1.37 from the parallelogram approach vs. experimental exposures, respectively, showing a good agreement. This quantitative inter-species extrapolation approach will be further explored for the clarification of metabolic rates/pharmacokinetics and the AUC of other genotoxic electrophilic compounds/metabolites, and has a potential to reduce and refine animal experiments. - Highlights: • In vitro metabolism to in vivo dose extrapolation of butadiene metabolites was proposed. • A parallelogram approach was introduced to estimate dose (AUC) in humans and rodents. • AUC of diepoxybutane predicted in humans was 0.078 nM h/ppm h

  14. Theoretical Kinetics Analysis for $\\dot{H}$ Atom Addition to 1,3-Butadiene and Related Reactions on the $\\dot{C}$4H7 Potential Energy Surface

    Energy Technology Data Exchange (ETDEWEB)

    Li, Yang [National Univ. of Ireland, Galway (Ireland). Combustion Chemistry Centre; Klippenstein, Stephen J. [Argonne National Lab. (ANL), Argonne, IL (United States). Chemical Sciences and Engineering Division; Zhou, Chong-Wen [Beihang Univ., Beihang (China). School of Energy and Power Engineering; Curran, Henry J. [National Univ. of Ireland, Galway (Ireland). Combustion Chemistry Centre

    2017-09-29

    The oxidation chemistry of the simplest conjugated hydrocarbon, 1,3-butadiene, can provide a first step in understanding the role of poly-unsaturated hydrocarbons in combustion and, in particular, an understanding of their contribution towards soot formation. Based on our previous work on propene and the butene isomers (1-, 2- and isobutene), it was found that the reaction kinetics of H-atom addition to the C=C double bond plays a significant role in fuel consumption kinetics and influences the predictions of high-temperature ignition delay times, product species concentrations and flame speed measurements. In this study, the rate constants and thermodynamic properties for $\\dot{H}$-atom addition to 1,3-butadiene and related reactions on the $\\dot{C}$4H7 potential energy surface have been calculated using two different series of quantum chemical methods and two different kinetic codes. Excellent agreement is obtained between the two different kinetics codes. The calculated results including zero point energies, single point energies, rate constants, barrier heights and thermochemistry are systematically compared among the two quantum chemical methods. 1-methylallyl ($\\dot{C}$4H71-3) and 3-buten-1- yl ($\\dot{C}$4H71-4) radicals and C2H4 + $\\dot{C}$2H3 are found to be the most important channels and reactivity promoting products, respectively. We calculated that terminal addition is dominant (> 80%) compared to internal $\\dot{H}$-atom addition at all temperatures in the range 298 – 2000 K. However, this dominance decreases with increasing temperature. The calculated rate constants for the bimolecular reaction C4H6 + $\\dot{H}$ → products and C2H4 + $\\dot{C}$2H3 → products are in excellent agreement with both experimental and theoretical results from the literature. For selected C4 species the

  15. Synthesis, structure and reactivity study of magnesium amidinato complexes derived from carbodiimides and N,N'-bis(2,6-diisopropylphenyl)-1,4-diaza-butadiene ligands.

    Science.gov (United States)

    Anga, Srinivas; Bhattacharjee, Jayeeta; Harinath, Adimulam; Panda, Tarun K

    2015-01-21

    We report an amidinato ligand-supported series of magnesium complexes obtained from the insertion of a magnesium-carbon bond into a carbon-nitrogen double bond of different carbodiimides and α-diimine ligands. The magnesium complexes [Mg(CH2Ph){CyN[double bond, length as m-dash]C(CH2Ph)NCy}]2 (), [Mg(CH2Ph){(i)PrN[double bond, length as m-dash]C(CH2Ph)N(i)Pr}]2 () and the homoleptic [Mg{(t)BuN[double bond, length as m-dash]C(CH2Ph)N(t)Bu}2] () (Cy = cyclohexyl, (i)Pr = isopropyl, (t)Bu = tert-butyl) were prepared by the reaction of dibenzyl magnesium [Mg(CH2Ph)2(Et2O)2] with the respective carbodiimides either in 1 : 1 or 1 : 2 molar ratio in toluene. The analogous reaction of [Mg(CH2Ph)2(Et2O)2] with the N,N'-bis(2,6-diisopropylphenyl)-1,4-diaza-1,3-butadiene (Dipp2DAD) ligand afforded the corresponding homoleptic magnesium complex [Mg{DippN[double bond, length as m-dash]C(CH2Ph)CH2NDipp}2] () (Dipp = 2,6 diisopropylphenyl) in good yield. The solid-state structures of magnesium complexes were confirmed by single-crystal X-ray diffraction analysis. It was observed that in each case, a magnesium-carbon bond was inserted into the carbon-nitrogen double bond of either carbodiimides or Dipp2DAD resulting in a monoanionic amido-imino ligand. In a further reaction between and N-aryliminopyrrolyl ligand 2-(2,6-(i)Pr2C6H3N[double bond, length as m-dash]CH)C4H3NH (ImpDipp-H) in 1 : 2 molar ratio, a new magnesium complex [Mg(ImpDipp)2{CyN[double bond, length as m-dash]C(CH2Ph)NHCy}] (), with one amidinato and two aryliminopyrrolyl ligands in the coordination sphere, was obtained in good yield. In contrast, the homoleptic magnesium complex reacted with one equivalent of N-aryliminopyrrolyl ligand (ImpDipp-H) to produce another mixed ligated magnesium complex [Mg{DippN[double bond, length as m-dash]C(CH2Ph)CH2NDipp}(ImpDipp)] (), with a benzylated DAD ligand and aryliminopyrrolyl ligands in the coordination sphere. Further reaction of complex with benzyl alcohol

  16. Use of laser-induced breakdown spectroscopy for the determination of polycarbonate (PC) and acrylonitrile-butadiene-styrene (ABS) concentrations in PC/ABS plastics from e-waste.

    Science.gov (United States)

    Costa, Vinicius Câmara; Aquino, Francisco Wendel Batista; Paranhos, Caio Marcio; Pereira-Filho, Edenir Rodrigues

    2017-12-01

    Due to the continual increase in waste generated from electronic devices, the management of plastics, which represents between 10 and 30% by weight of waste electrical and electronic equipment (WEEE or e-waste), becomes indispensable in terms of environmental and economic impacts. Considering the importance of acrylonitrile-butadiene-styrene (ABS), polycarbonate (PC), and their blends in the electronics and other industries, this study presents a new application of laser-induced breakdown spectroscopy (LIBS) for the fast and direct determination of PC and ABS concentrations in blends of these plastics obtained from samples of e-waste. From the LIBS spectra acquired for the PC/ABS blend, multivariate calibration models were built using partial least squares (PLS) regression. In general, it was possible to infer that the relative errors between the theoretical or reference and predicted values for the spiked samples were lower than 10%. Copyright © 2017 Elsevier Ltd. All rights reserved.

  17. Effect of adding of the styrene-butadiene-styrene (SBS) copolymer in chemical and rheological properties of the brazilian asphalt; Efeito da adicao de SBS nas propriedades quimicas e reologicas de asfalto oriundo de petroleo brasileiro

    Energy Technology Data Exchange (ETDEWEB)

    Lucena, M.C.C.; Soares, S.A. [Ceara Univ., Fortaleza, CE (Brazil). Dept. de Quimica Organica e Inorganica]. E-mail: mccl@dqoi.ufc.br; sas@ufc.br; Soares, J.B. [Ceara Univ., Fortaleza, CE (Brazil). Dept. de Engenharia de Transportes]. E-mail: jsoares@det.ufc.br

    2003-07-01

    Chemical and rheological characterization of the asphalt cement (AC) from the Fazenda Alegre petroleum, and the effect of adding 4.5% of the styrene-butadiene-styrene (SBS) copolymer were investigated. Structural characteristics were analyzed by infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR). A structure similar to the Arabian and Venezuelan petroleum was observed. The simulated aging led to structural modification noticed by the increment in the carbonyl and sulphoxide groups. Thermogravimetry (TGA) showed that SBS did not affect the AC thermal decomposition at both inert and oxidative atmosphere. However, the differential scanning calorimetry (DSC) showed a decrease in the glass transition temperature of the material when SBS was added. The effect of SBS on the absolute viscosity revealed that SBS is not an inert additive and causes an increase in viscosity, in a nonlinear fashion. The commonly found Newtonian behavior of asphalt binders under high temperatures was also found on the SBS modified binder. Dynamic mechanical tests have shown that SBS increases the binder performance grade. (author)

  18. Sum Frequency Generation Vibrational Spectroscopy of 1,3-Butadiene Hydrogenation on 4 nm Pt@SiO 2 , Pd@SiO 2 , and Rh@SiO 2 Core–Shell Catalysts

    KAUST Repository

    Krier, James M.

    2015-01-14

    © 2014 American Chemical Society. 1,3-Butadiene (1,3-BD) hydrogenation was performed on 4 nm Pt, Pd, and Rh nanoparticles (NPs) encapsulated in SiO2 shells at 20, 60, and 100 °C. The core-shells were grown around polyvinylpyrrolidone (PVP) coated NPs (Stöber encapsulation) prepared by colloidal synthesis. Sum frequency generation (SFG) vibrational spectroscopy was performed to correlate surface intermediates observed in situ with reaction selectivity. It is shown that calcination is effective in removing PVP, and the SFG signal can be generated from the metal surface. Using SFG, it is possible to compare the surface vibrational spectrum of Pt@SiO2 (1,3-BD is hydrogenated through multiple paths and produces butane, 1-butene, and cis/trans-2-butene) to Pd@SiO2 (1,3-BD favors one path and produces 1-butene and cis/trans-2-butene). In contrast to Pt@SiO2 and Pd@SiO2, SFG and kinetic experiments of Rh@SiO2 show a permanent accumulation of organic material.

  19. Influence of pyrolytic carbon black and pyrolytic oil made from used tires on the curing and (dynamic mechanical properties of natural rubber (NR/styrene-butadiene rubber (SBR blends

    Directory of Open Access Journals (Sweden)

    F. Karabork

    2016-01-01

    Full Text Available Pyrolytic carbon black (CBp and pyrolytic oil (Op made from used tires were used in natural rubber (NR/styrene-butadiene rubber (SBR blends. The effects of CBp and Op on the processing properties, the mechanical properties and the dynamic mechanical properties of the NR/SBR blends were investigated and compared with a control sample that was prepared with N550 and commercial process oil. It was found that the effect of CBp on the processing properties of the NR/SBR blends was similar to that of N550. With the increase of the CBp content, the curing properties of the NR/SBR blends changed little. The reinforcing effect of CBp was inferior to that of N550. With the increase of the CBp content, the tensile strength, tear strength and modulus at 100% elongation of the NR/SBR vulcanizates decreased significantly. Dynamic mechanical properties of the NR/SBR blends were also affected and all samples comprising CBp have a higher tan δ than control sample. It is suggested that the low surface area and high ash content of CBp strongly effects all of these property changes of the NR/SBR blends. The morphology and distribution of the carbon black particles are studied using a scanning electron microscope. It was also found that with the increase of the Op content, the properties of the NR/SBR blends were strongly affected due to the high sulfur content of Op, which produced a high crosslinking density.

  20. Influence of Type and Amount of Carbon in Cigarette Filters on Smokers’ Mouth Level Exposure to “Tar”, Nicotine, 1,3-Butadiene, Benzene, Toluene, Isoprene, and Acrylonitrile

    Directory of Open Access Journals (Sweden)

    Nother Kathryn

    2016-04-01

    Full Text Available Activated carbons are effective adsorbents for many volatile organic compounds and are used in cigarette filters to remove selected smoke toxicants. Polymer-derived carbon is more effective in removing many vapour phase toxicants found in cigarette smoke than coconut-shell-derived carbon. We compared mouth-level exposure to “tar”, nicotine and five vapour phase constituents (1,3- butadiene, benzene, toluene, isoprene, acrylonitrile in two groups of Romanian smokers of 4-mg or 8-mg International Organization for Standardization (ISO “tar” bands. Test cigarettes with 4 and 8 mg ISO “tar” were manufactured for the study with two target levels of polymer-derived carbon (30 mg and 56 mg, along with control cigarettes containing a target level of 56 mg of coconut-shell-derived carbon in both “tar” bands. No significant differences were found between mouth-level exposure to “tar” or nicotine yields obtained from control and test products (p > 0.05 in either ISO “tar” band. Mouth-level exposure to each of the five vapour phase constituents was significantly lower from the test products with polymer-derived carbon (p < 0.0001 than from control cigarettes with coconut-shell-derived carbon, by an average of 25% with 30 mg polymer-derived carbon and around 50% with 56 mg. [Beitr. Tabakforsch. Int. 27 (2016 40-53

  1. An Investigation on the Extraction and Quantitation of a Hexavalent Chromium in Acrylonitrile Butadiene Styrene Copolymer (ABS) and Printed Circuit Board (PCB) by Ion Chromatography Coupled with Inductively Coupled Plasma Atomic Emission Spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Nam, Sang Ho; Kim, Yu Na [Mokpo National University, Muan (Korea, Republic of)

    2012-06-15

    A hexavalent chromium (Cr (VI)) is one of the hazardous substances regulated by the RoHS. The determination of Cr (VI) in various polymers and printed circuit board (PCB) has been very important. In this study, the three different analytical methods were investigated for the determination of a hexavalent chromium in Acrylonitrile Butadiene Styrene copolymer (ABS) and PCB. The results by three analytical methods were obtained and compared. An analytical method by UV-Visible spectrometer has been generally used for the determination of Cr (VI) in a sample, but a hexavalent chromium should complex with diphenylcarbazide for the detection in the method. The complexation did make an adverse effect on the quantitative analysis of Cr (VI) in ABS. The analytical method using diphenylcarbazide was also not applicable to printed circuit board (PCB) because PCB contained lots of irons. The irons interfered with the analysis of hexavalent chromium because those also could complex with diphenylcarbazide. In this study, hexavalent chromiums in PCB have been separated by ion chromatography (IC), then directly and selectively detected by inductively coupled plasma atomic emission spectrometry (ICP-AES). The quantity of Cr (VI) in PCB was 0.1 mg/kg

  2. Effect of γ-aminopropyltriethoxy silane (γ-APS) coupling agent on mechanical and morphological properties of high density polyethylene (HDPE)/acrylonitrile butadiene rubber (NBR)/palm pressed fibre (PPF) composites

    Science.gov (United States)

    Norizan, Nabila Najwa; Santiagoo, Ragunathan; Ismail, Hanafi

    2017-07-01

    The fabrication of High Density Polyethylene (HDPE)/ Acrylonitrile-butadiene rubber (NBR)/ Palm Pressed Fibre (PPF) composite were investigated. The effect of γ-Aminopropyltriethoxy Silane (APS) as coupling agent on the properties of HDPE/ NBR/ PPF composite were studied. The composites were melt mixed using heated two roll mill at 180°C and speed of 15rpm with six different loading (100/0/10, 80/20/10, 70/30/10, 60/40/10, 50/50/10, and 40/60/10). The effects of γ-APS silane on mechanical, and morphological properties were examined using universal tensile machine (UTM) and scanning electron microscopy (SEM), respectively. Tensile strength and Young's modulus of HDPE/ NBR/ PPF composites decrease with increasing of NBR loading, whilst increasing the elongation at break. However, treated composites have resulted 3% to 29%, and 9% to 19%, higher in tensile strength and young's modulus compared to untreated composites. This was due to the better adhesion between HDPE/ NBR matrices and PPF filler with the presence of silanol moieties. From the morphological study, the micrograph of treated composites has proved the well bonded and good attachment of PPF filler with HDPE/ NBR matrices which resulted to better tensile strength to the HDPE/ NBR/ PPF composites.

  3. Tunable regioselectivity in 1,3-butadiene polymerization by using 2,6-bis(dimethyl-2-oxazolin-2-yl)pyridine incorporated transition metal (Cr, Fe and Co) catalysts

    KAUST Repository

    Gong, Dirong

    2015-05-21

    Tridentate complexes Cr(III)Cl3L, [L = 2,6-bis(dimethyl-2-oxazolin-2-yl) pyridine], Fe(III)Cl3L, Fe(II)Cl2L and Co(II)Cl2L have been prepared and fully characterized. The solid structures of Cr(III)Cl3L, Fe(III)Cl3L and Co(II)Cl2L have been revealed by single crystal X-ray diffraction, and the Cr(III)Cl3L and Fe(III)Cl3L complexes both exhibit a distorted octahedral geometry, while the Co(II)Cl2L complex has a trigonal bipyramidal conformation. Four complexes have been examined in regioselective polymerization of butadiene in combination with MAO in toluene at room temperature. The trans-1,4, cis-1,4 enchainment of resultant polybutadiene are controlled by the metal center. Activated by MAO, complex Cr(III)Cl3L produces high level of trans-1,4 selectivity (trans-1,4 up to 93.3%) with moderate polymer yield, complexes Fe(III)Cl3L and Fe(II)Cl2L both show equal cis-1,4 and trans-1,4 with minor 1,2 selectivity (<10%), and Co(II)Cl2L catalyst displays predominated cis-1,4 selectivity, which can be shifted to 1,2 selectivity by adding PPh3 as an additive. Thus, tuning of the cis-1,4, trans-1,4 and 1,2 selectivity in full range via central metal and additive chosen by these 2,6-bis(dimethyl-2-oxazolin-2-yl) pyridine supported catalysts has been achieved. © 2015 Elsevier B.V. All rights reserved.

  4. In vivo doses of butadiene epoxides as estimated from in vitro enzyme kinetics by using cob(I)alamin and measured hemoglobin adducts: an inter-species extrapolation approach.

    Science.gov (United States)

    Motwani, Hitesh V; Törnqvist, Margareta

    2014-12-15

    1,3-Butadiene (BD) is a rodent and human carcinogen. In the cancer tests, mice have been much more susceptible than rats with regard to BD-induced carcinogenicity. The species-differences are dependent on metabolic formation/disappearance of the genotoxic BD epoxy-metabolites that lead to variations in the respective in vivo doses, i.e. "area under the concentration-time curve" (AUC). Differences in AUC of the most gentoxic BD epoxy-metabolite, diepoxybutane (DEB), are considered important with regard to cancer susceptibility. The present work describes: the application of cob(I)alamin for accurate measurements of in vitro enzyme kinetic parameters associated with BD epoxy-metabolites in human, mouse and rat; the use of published data on hemoglobin (Hb) adduct levels of BD epoxides from BD exposure studies on the three species to calculate the corresponding AUCs in blood; and a parallelogram approach for extrapolation of AUC of DEB based on the in vitro metabolism studies and adduct data from in vivo measurements. The predicted value of AUC of DEB for humans from the parallelogram approach was 0.078 nM · h for 1 ppm · h of BD exposure compared to 0.023 nM · h/ppm · h as calculated from Hb adduct levels observed in occupational exposure. The corresponding values in nM · h/ppm · h were for mice 41 vs. 38 and for rats 1.26 vs. 1.37 from the parallelogram approach vs. experimental exposures, respectively, showing a good agreement. This quantitative inter-species extrapolation approach will be further explored for the clarification of metabolic rates/pharmacokinetics and the AUC of other genotoxic electrophilic compounds/metabolites, and has a potential to reduce and refine animal experiments. Copyright © 2014 Elsevier Inc. All rights reserved.

  5. New insights into the effects of styrene-butadiene-styrene polymer modifier on the structure, properties, and performance of asphalt binder: The case of AP-5 asphalt and solvent deasphalting pitch

    Energy Technology Data Exchange (ETDEWEB)

    Nciri, Nader, E-mail: nader.nciri@koreatech.ac.kr [Department of Energy, Materials, and Chemical Engineering, Korea University of Technology and Education, 1600 Chungjeol-ro, Byeongcheon-myeon, Dongnam-gu, Cheonan-City, Chungnam-Province 330-708 (Korea, Republic of); Kim, Namho [Department of Architectural Engineering, Korea University of Technology and Education, 1600 Chungjeol-ro, Byeongcheon-myeon, Dongnam-gu, Cheonan-City, Chungnam-Province 330-708 (Korea, Republic of); Cho, Namjun, E-mail: njuncho@koreatech.ac.kr [Department of Energy, Materials, and Chemical Engineering, Korea University of Technology and Education, 1600 Chungjeol-ro, Byeongcheon-myeon, Dongnam-gu, Cheonan-City, Chungnam-Province 330-708 (Korea, Republic of)

    2017-06-01

    This paper deals with the poorly understood effects of styrene-butadiene-styrene (SBS) copolymer on the bitumen performance. It focuses on determining the impact of various concentrations (e.g., 0, 4, 8, and 12 wt. %) of SBS on the attributes of two types of asphalt namely AP-5 asphalt and solvent deasphalting (SDA) pitch. The unmodified and modified binders were investigated in terms of their chemical compositions, microstructures, thermo-analytical behaviors, and physical properties. The intricate chemical compositions were evaluated by elemental analysis and thin layer chromatography-ionization detection (TLC-FID). Fourier transform infrared (FT-IR) and nuclear magnetic resonance (NMR) spectroscopies, scanning electron microscopy (SEM), and X-ray diffraction (XRD) were utilized to examine the microstructures. Whereas, thermal characteristics were evaluated by thermogravimetric analysis (TGA/DTGA) and differential scanning calorimetry (DSC). The physical behaviors were monitored through the softening point, penetration, viscosity, and ductility tests. The findings showed that the blending of asphalt with different amounts of SBS resulted into different rheological behaviors. This was reflected from the difference in the SARA (i.e., saturates, aromatics, resins, and asphaltenes) compositions and colloidal instability indexes of the modified asphalts. SEM exhibited a continuous asphalt phase with distributed SBS particles, a continuous polymer phase with distributed asphalt globules, or two interconnected continuous phases. FT-IR, {sup 1}H {sup 13}C NMR, and XRD data revealed that the AP-5 asphalt and SDA pitch experienced a number of distinct structural changes. TGA/DSC studies determined the occurrence of diverse events during thermal treatment. It is concluded that the degree of SBS modification depends strongly on SARA composition and polymer content. If the polymers are molded at higher concentrations along with aromatics-rich SDA pitches, then the mixtures

  6. Comparison of sodium naphthenate and air-ionization corona discharge as surface treatments for the ethylene-tetrafluoroethylene polymer (ETFE) to improve adhesion between ETFE and acrylonitrile-butadiene-styrene polymer (ABS) in the presence of a cyanoacrylate adhesive (CAA)

    Science.gov (United States)

    Lucía Johanning-Solís, Ana; Stradi-Granados, Benito A.

    2014-09-01

    This study compares two ethylene-tetrafluoroethylene (ETFE) surface activation treatments, namely chemical attack with a solution of sodium naphthenate and plasma erosion via air-ionization corona discharge in order to improve the adhesive properties of the ETFE. An experimental design was prepared for both treatments in order to assess the effect of the treatment characteristics on the tensile load needed to break the bond between the ETFE and the acrylonitrile-butadiene-styrene polymer (ABS) formed with a cyanoacrylate adhesive (CAA) applied between them. The reason for the selection of this problem is that both polymers are frequently used in the biomedical industry for their properties, and they need to be joined firmly in biomedical devices, and the cyanoacrylate adhesive is the adhesive traditionally used for fluoropolymers, in this case the ETFE, and the same CAA has also shown good adhesion with ABS. However, the strength of the bond for the triplet ETFE-CAA-ABS has not been reported and the improvement of the strength of the bond with surface treatments is not found in scholarly journals for modern medical devices such as stents and snares. Both treatments were compared based on the aforementioned design of experiments. The case where ETFE receives no surface treatment serves as the reference. The results indicated that the three factors evaluated (initial drying of the material, temperature of the chemical bath, and immersion time), and their interactions have no significant effect over the tensile load at failure (tensile strength) of the adhesive bond being evaluated. For the air-ionization corona discharge treatment, two factors were evaluated: discharge exposition time and air pressure. The results obtained from this experimental design indicate that there is no significant difference between the levels of the factors evaluated. These results were unexpected as the ranges used were representative of the maximum ranges permissible in manufacturing

  7. Comparative study of the monomer grafting: ethylene, acetylene, 1,3-butadiene and estyrene in the matrix of recycled polytetrafluoroethylene (PTFE); Estudo comparativo da enxertia dos monomeros: etileno, acetileno, 1,3-butadieno e estireno na matriz de politetrafluoroetileno (PTFE) reciclado

    Energy Technology Data Exchange (ETDEWEB)

    Ikari, Carolina T.; Rosner, Gerhardyne O.; Oliveira, Ana C.F. [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Centro de Quimica e Meio Ambiente (CQMA); Faculdades Oswaldo Cruz, Sao Paulo, SP (Brazil); Ferreto, Helio F.R.; Lima, Luiz F.C.P.; Lugao, Ademar B., E-mail: hferreto@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Centro de Quimica e Meio Ambiente (CQMA); Moreira, Otavio M. [Faculdades Oswaldo Cruz, Sao Paulo, SP (Brazil)

    2009-07-01

    In this study it is used the recycled polytetrafluoroethylene (PTFE), that with the gamma radiation under inert atmosphere or in presence of air, it is obtained free radicals and a posterior the monomer grafting (ethylene, acetylene, styrene or 1.3 butadiene), obtaining the copolymer polytetrafluoroethylene-g-monomer. It is studied the obtention of the polymer by two methods: by direct way, via grafting, where the polymer is irradiated in presence of monomer, and via grafting when the polymer is irradiated in absence of monomer and under inert or air. The characterization of the copolymer was performed by the techniques of infrared region absorption spectroscopy with Fourier transformation (FTIR), thermogravimetric (TGA) and derivative thermogravimetry (DTG), and percentage of mass grafting (DOG)

  8. Development of analytical methods for the gas chromatographic determination of 1,2-epoxy-3-butene, 1,2:3,4-diepoxybutane, 3-butene-1,2-diol, 3,4-epoxybutane-1,2-diol and crotonaldehyde from perfusate samples of 1,3-butadiene exposed isolated mouse and rat livers

    Energy Technology Data Exchange (ETDEWEB)

    Bhowmik, S.; Schuster, A.; Filser, J.G.

    2003-07-01

    Mutagenicity and carcinogenicity of 1,3-butadiene (BD) highly probably results from epoxide metabolites as 1,2-epoxy-3-butene (EB), 1,2:3,4-diepoxybutane (DEB) and 3,4-epoxybutane-1,2-diol (EBD). A further metabolite crotonaldehyde (CA) has also been discussed to be relevant. So far, in BD exposed rodents only EB and DEB concentrations had been quantified. However, the methods used were either not very sensitive or instrumentally expensive. Therefore, the goal of the present work was to establish simple analytical methods selective and sensitive enough to determine all of these compounds and a further secondary BD intermediate, 3-butene-1,2-diol (B-diol), in BD exposed rodent livers. The once-through perfused liver system was chosen for testing the applicability of the methods to be developed, since it enables BD exposures of this quantitatively most relevant metabolising organ near to the in-vivo situation. All the metabolites were extracted from the aqueous perfusion medium and analysed using a gas chromatograph equipped with a mass selective detector (GC/MS) in the PCI mode. (orig.)

  9. Valorisation de la coupe C4 de vapocraquage via l'hydrogénation du butadiène, l'isomérisation des butènes et la métathèse, en MTBE ou en propylène Upgrading the C4 Cut from Steam Cracking via the Hydrogenation of Butadiene, the Isomerization of Butenes and Metathesis Into Mtbe Or Propylene

    Directory of Open Access Journals (Sweden)

    Chaumette S.

    2006-11-01

    Full Text Available Le surplus de butadiène au niveau mondial contraint les pétrochimistes à recycler la coupe C4 au vapocraqueur. De plus en plus, le butadiène est hydrogéné avant de recraquer toute la coupe. Une fois hydrogénée, cette coupe peut être beaucoup mieux valorisée, soit en MTBE avec isomérisation des n-butènes (procédé ISO-4, soit en propylène et MTBE en utilisant le procédé META-4. L'étude technico-économique montre que cette dernière voie offre la meilleure rentabilité (TRI = 21,5 %. Si le vapocraqueur est intégré à une raffinerie, les butènes peuvent également être transformés en alkylats ou en MTBE, pour répondre à une demande en octane ou en oxygénés pour les carburants. Ces diverses voies de valorisation sont plus intéressantes que la production de MTBE à partir des butanes via la déshydrogénation de l'isobutane ou que la production du propylène par déshydrogénation du propane. Une étude de sensibilité aux différents prix des produits envisagés permet d'établir des courbes d'isorentabilités, délimitant des zones de prix favorables à l'un ou l'autre des produits, pris deux à deux. The evolution of the outlets for C4 cuts from steam cracking shows quite contradictory results. On one hand, European and Asian petrochemists are more constrained to recycle this type of effluent, which contains butadiene and isobutene, to the steam cracker. Likewise, the demand for isobutene for MTBE production is such that it has to be produced by the dehydrogenation of isobutane. This situation is effectively caused by the surplus of butadiene, a by-product of ethylene, and for which the demand is not increasing as fast as the demand for ethylene. To improve cracking performances during the recycling of the C4 Cut, butadiene is more and more selectively hydrogenated. Under these conditions, rather than cracking it, the new processes could make it possible to better upgrade it. Indeed, after selective hydrogenation, most

  10. Influência do agente de cloração do catalisador à base de veodímio e da razão molar Cl: Nd na polimerização do butadieno Influence of the chlorinating agent of neodymium based catalysts and Cl: Nd molar ratio on butadiene polymerization

    Directory of Open Access Journals (Sweden)

    Cintia N. Ferreira

    2009-06-01

    Full Text Available Neste trabalho foi utilizado um sistema catalítico composto por hidreto de diisobutilalumínio (DIBAH, versatato de neodímio (NdV e um agente de cloração para avaliar a influência da fonte de cloro e da razão molar Cl:Nd nas características da reação de polimerização (conversão e constante de velocidade de propagação e do polibutadieno (massa molecular e microestrutura. Os agentes de cloração estudados foram cloreto de t-butila (t-BuCl, sesquicloreto de etilalumínio (EASC e cloreto de dietilalumínio (DEAC. As razões molares Cl:Nd utilizadas foram: 1:1, 3:1 e 5:1 para o t-BuCl; 0,5:1, 1:1 e 3:1 para o EASC e 1:1, 1,5:1, 3:1 e 5:1 para o DEAC. Foi observada a existência, para cada agente de cloração, de um valor ótimo de razão molar Cl:Nd para o qual a conversão foi máxima. O DEAC apresentou uma maior conversão em relação aos outros agentes de cloração; em contrapartida, o t-BuCl produziu polibutadienos com maior teor de unidades 1,4-cis e maior massa molecular (n e wIn this work catalyst systems consisting of diisobutylaluminium hydride (DIBAH, neodymium versatate (NdV and a chlorinating agent were employed to study the influence of the chloride source and Cl:Nd molar ratio on 1,3-butadiene polymerization and polybutadiene's characteristics (molecular weight and microstructure. The chloride sources studied were t-butyl chloride, ethylaluminium sesquichloride (EASC and diethylaluminium chloride (DEAC. The Cl:Nd molar ratios used were 1:1, 3:1 e 5:1 for t-butyl chloride; 0.5:1, 1:1 and 3:1 for EASC and 1:1, 1.5:1, 3:1 and 5:1 for DEAC. A maximum value of Cl:Nd molar ratio exists. Moreover, DEAC showed to be more reactive than EASC and t-BuCl but t-BuCl produced higher molecular weight and cis-1,4 units contents.

  11. Variation of long periodicity in blends of styrene butadiene, styrene ...

    Indian Academy of Sciences (India)

    1. Instituto de Macromoleculas, Universidade Federal do Rio de Janeiro,. Centro de Tecnologia, Bl. J, Ilha do Fundo, 21945-970, Rio de Jeneiro, RJ, Brazil. 2. Department of Physics, Yuvaraja's College, University of Mysore, Mysore 570 005, India. 3. Department of Studies in Physics, University of Mysore, Manasagangothri,.

  12. Variation of long periodicity in blends of styrene butadiene, styrene ...

    Indian Academy of Sciences (India)

    Instituto de Macromoleculas, Universidade Federal do Rio de Janeiro, Centro de Tecnologia, Bl. J, Ilha do Fundo, 21945-970, Rio de Jeneiro, RJ, Brazil; Department of Physics, Yuvaraja's College, University of Mysore, Mysore 570 005, India; Department of Studies in Physics, University of Mysore, Manasagangothri, ...

  13. 29 CFR 1910.1051 - 1,3-Butadiene.

    Science.gov (United States)

    2010-07-01

    ... an employee including: (A) The name of the employee, (B) Type of respirator, (C) Brand and size of...) Availability. (i) The employer, upon written request, shall make all records required to be maintained by this...

  14. Molecular simulation of gas solubility in nitrile butadiene rubber

    OpenAIRE

    Khawaja, M.; Sutton, AP; Mostofi, AA

    2016-01-01

    Molecular simulation is used to compute the solubility of small gases in nitrile bu- tadiene rubber (NBR) with a Widom particle-insertion technique biased by local free volume. The convergence of the method is examined as a function of the number of snapshots upon which the insertions are performed and the number of insertions per snapshot, and is compared to the convergence of the unbiased Widom insertion technique. The effect of varying the definition of the local free volume is also invest...

  15. Carboxylated nitrile butadiene rubber/hybrid filler composites

    Directory of Open Access Journals (Sweden)

    Ahmad Mousa

    2012-08-01

    Full Text Available The surface properties of the OSW and NLS are measured with the dynamic contact-angle technique. The x-ray photoelectron spectroscopy (XPS of the OSW reveals that the OSW possesses various reactive functional groups namely hydroxyl groups (OH. Hybrid filler from NLS and OSW were incorporated into carboxylated nitrile rubber (XNBR to produce XNBR hybrid composites. The reaction of OH groups from the OSW with COOH of the XNBR is checked by attenuated total reflectance spectra (ATR-IR of the composites. The degree of curing ΔM (maximum torque-minimum torque as a function of hybrid filler as derived from moving die rheometer (MDR is reported. The stress-strain behavior of the hybrid composites as well as the dynamic mechanical thermal analysis (DMTA is studied. Bonding quality and dispersion of the hybrid filler with and in XNBR are examined using scanning-transmission electron microscopy (STEM in SEM.

  16. Functionalization of [60] fullerene with butadienes: A DFT study

    Energy Technology Data Exchange (ETDEWEB)

    Beheshtian, Javad [Department of Chemistry, Shahid Rajaee Teacher Training University, P.O. Box: 16875-163, Tehran (Iran, Islamic Republic of); Peyghan, Ali Ahmadi, E-mail: ahmadi.iau@gmail.com [Young Researchers Club, Islamic Azad University, Islamshahr Branch, Tehran (Iran, Islamic Republic of); Bagheri, Zargham [Physics group, Science department, Islamic Azad University, Islamshahr Branch, P.O. Box: 33135-369, Islamshahr, Tehran (Iran, Islamic Republic of)

    2012-09-01

    Highlights: Black-Right-Pointing-Pointer Reaction of C{sub 60} with 2,3-dimethylbutadiene (DMB) is theoretically investigated. Black-Right-Pointing-Pointer The HOMO of DMB interacts with the LUMO of C{sub 60} via a Diels Alder reaction. Black-Right-Pointing-Pointer Work function of C{sub 60} is decreased by increasing the number of DMB molecules. Black-Right-Pointing-Pointer The reaction may facilitate the field electron emission from C{sub 60} surface. - Abstract: We have performed a density functional study on the reaction of C{sub 60} fullerene with one to six 2,3-dimethylbutadiene (DMB) molecule(s) which has previously been investigated by experimental researchers. Based on the obtained results, it has been found that (1) the reaction is regioselective, so that the DMB molecule prefers to be adsorbed atop a C-C bond which is shared between two hexagonal rings of C{sub 60} (in good agreement with the experimental results) with reaction energy of -0.98 eV; (2) the HOMO of DMB interacts with the LUMO of C{sub 60} via a Diels Alder reaction; (3) the energy of reaction and work function of C{sub 60} are decreased by increasing the number of adsorbed DMB molecules; (4) the HOMO-LUMO energy gap of C{sub 60} is slightly changed upon the reaction; (5) the reaction reduces the potential barrier of the field electron emission of C{sub 60} surface.

  17. Kinetics of CN reactions with allene, butadiene, propylene and acrylonitrile

    Science.gov (United States)

    Butterfield, Michelle T.; Yu, T.; Lin, M. C.

    1993-01-01

    The two-laser pump-probe technique has been used to study the kinetics of the reaction of CN radicals with C 3H 6, CD 3C 2H 3, C 3D 6, C 2H 3CN, C 3H 4 and C 4H 6 at temperatures between 297 and 740 K. CN was generaged by 248-nm photolysis of ICN. Laser-induced fluorescence of the CN radical has been used for its detection by CN (B←X) excitation. The values for the rate constants, given in units of cm 3/s, are reported as: k(C 3H 6)=10 -9.88±0.10exp(+244±96.3/ T), k(C 3H 3D 3) = 10 -9.76±0.04 exp (+143.4±35.1/ T), k(C 3D 6)=10 -9.87±0.05exp(+231.4±47.01/ T, k(C 2H 3CN)=10 -10.52±0.02exp(+103.6±20.3/ T), k(C 3H 4)=10 -9.58±0.08 ×exp(+167.4±73.7/ T), k(C 4H 6)=10 -9.59±0.04exp(+169.2±33.1/ T). The absolute rates of CN reactions with CH 3CHCH 2, CD 3CHCH 2 and CD 3CDCD 2 are essentially the same and are somewhat faster than that of the CN+C 2H 4 reaction. This suggests that the CN+C 3H 6 reaction occurs primarily by addition to the unsaturated bond and the CH 3 group enhances the addition process slightly. The rate of the CN+CH 2CHCN reaction, however, was found to be a factor of six slower than that of CN+C 2H 4, indicating a substantial electron withdrawing effect of the CN group in vinyl cyanide which results in the reduction in the addition rate. The rates for CN reaction with CH 2CCH 2 and CH 2CHCHCH 2 are approximately the same and are twice that of CN+C 2H 4.

  18. Caracterização de artefatos elastoméricos obtidos por revulcanização de resíduo industrial de SBR (copolímero de butadieno e estireno Characterization of elastomeric artifacts obtained by revulcanization of SBR industrial waste (Styrene-butadiene Rubber

    Directory of Open Access Journals (Sweden)

    Tatiana Weber

    2011-01-01

    Full Text Available A reciclagem de resíduos de borracha é de extrema importância nos dias de hoje, tanto em relação aos impactos ambientais quanto à conservação de energia. Considerando que a maioria dos trabalhos publicados atualmente se refere à reciclagem de pneus, o objetivo deste trabalho foi desenvolver e caracterizar formulações contendo um tipo de resíduo industrial, proveniente da fabricação de perfis automotivos, à base de copolímero de butadieno e estireno (SBR para possível aplicação na própria empresa. As composições foram preparadas e caracterizadas pela determinação das propriedades térmicas (calorimetria diferencial de varredura, reológicas (analisador de processamento de borracha, reométricas (reômetria de disco oscilatório, mecânicas (resistência à tração e ao rasgamento, químicas (densidade de ligações cruzadas e morfológicas (microscopia eletrônica de varredura. Os resultados obtidos para as composições foram comparados aos de uma amostra controle, de mesma composição, que foi fornecida pela empresa geradora do resíduo de SBR. Os resultados mecânicos indicaram que o processo de revulcanização proposto foi efetivo. Os valores dos parâmetros de tensão na ruptura e resistência ao rasgamento foram de 70 e 50%, respectivamente, em relação aos valores encontrados para a amostra controle, indicando a possibilidade do uso desse resíduo em artefatos de menor exigência técnica.The recycling of waste rubber has very important significances, such as protection of the environment and conservation of energy. Considering that most of published works concerning this subject are about tire recycling, the objective of this work was to develop and characterize formulations containing a type of industrial waste, from the manufacture of automotive profiles, based on styrene-butadiene rubber (SBR for possible application in the industry. The compositions were formulated and characterized by thermal (differential

  19. Recycling cycle of materials applied to acrylonitrile-butadiene-styrene/policarbonate blends with styrene-butadiene-styrene copolymer addition

    Science.gov (United States)

    Cândido, L. H. A.; Ferreira, D. B.; Júnior, W. Kindlein; Demori, R.; Mauler, R. S.

    2014-05-01

    The scope of this research is the recycling of polymers from mobile phones hulls discarded and the performance evaluation when they are submitted to the Recycling Cycle of Materials (RCM). The studied material was the ABS/PC blend in a 70/30 proportion. Different compositions were evaluated adding virgin material, recycled material and using the copolymer SBS as impact modifier. In order to evaluate the properties of material's composition, the samples were characterized by TGA, FTIR, SEM, IZOD impact strength and tensile strength tests. At the first stage, the presented results suggest the composition containing 25% of recycled material and 5% of SBS combines good mechanical performance to the higher content of recycled material and lower content of impact modifier providing major benefits to recycling plans. Five cycles (RCM) were applied in the second stage; they evidenced a decrease trend considering the impact strength. At first and second cycle the impact strength was higher than reference material (ABS/PC blend) and from the fourth cycle it was lower. The superiority impact strength in the first and second cycles can be attributed to impact modifier effect. The thermal tests and the spectrometry didn't show the presence of degradation process in the material and the TGA curves demonstrated the process stability. The impact surface of each sample was observed at SEM. The microstructures are not homogeneous presenting voids and lamellar appearance, although the outer surface presents no defects, demonstrating good moldability. The present work aims to assess the life cycle of the material from the successive recycling processes.

  20. 40 CFR 63.190 - Applicability and designation of source.

    Science.gov (United States)

    2010-07-01

    ...-styrene resins (MBS) (iii) Butadiene-furfural cotrimer, (iv) Methylmethacrylate-acrylonitrile-butadiene.... (1) Styrene-butadiene rubber production (butadiene and styrene emissions only). (2) Polybutadiene rubber production (butadiene emissions only). (3) The processes producing the agricultural chemicals...

  1. New dual-phase polymer electrolytes prepared from NBR/SBR lattices. [polyacryloNitrile-Butadiene Rubber/poly(Styrene-Butadiene) copolymer Rubber

    Energy Technology Data Exchange (ETDEWEB)

    Matsumoto, Morihiko; Ichino, Toshihiro; Rutt, J.S.; Nishi, Shiro (Nippon Telegraph and Telephone Corp., Tokyo (Japan). NTT Interdisciplinary Research Lab.)

    1993-10-01

    A new type of Li[sup +] ion conducting polymer electrolytes consisting of two phases, one of which is a highly polar region (impregnated with lithium salt solution), forming ion-conductive channels, while the other is a nonpolar region, forming supporting polymer matrices have been prepared from NBR/SBR lattices. TEM measurement and EDX analysis show evidence that dual-phase structure is constructed in the electrolyte. Ionic conductivity of the electrolyte increases with increase of lithium salt solution content. Maximum ionic conductivity of 2.2 [times] 10[sup [minus]3] S/cm is obtained at the lithium salt solution content of 60.5% (w/w). The electrolyte retains rubber-like film with good mechanical strength despite the presence of the solution.

  2. Dynamic Response of Acrylonitrile Butadiene Styrene Under Impact Loading (Open Access)

    Science.gov (United States)

    2016-03-16

    Fig. 3 Material build direction 0/90 orientation Fig. 4 Experimental setup prior to testing Fig. 2 ASTM D638-03 dog bone (International et al. 2004...deformation and fracture behaviour of Ti– 6Al–4V alloy loaded with high strain rate under various temperatures. Materials Science and Engineering A, 24...C. R., Walley, S. M., Proud, W. G., & Field, J. E. (2006). Mechanical behaviour of polymers at high rates of strain. Journal De Physique IV., 134, 949

  3. Dynamic Evaluation of Acrylonitrile Butadiene Styrene Subjected to High-Strain-Rate Compressive Loads

    Science.gov (United States)

    2014-12-01

    Conclusions 10 5. References 11 Distribution List 13 iv List of Figures Figure 1. ASTM D 638-03 dog bone...1. ASTM D 638-03 dog bone. When designing the specimen for tensile testing, it is important that the tensile specimen be built such that the...2006, 45 (1), 18–24. 8. Lee, W. S.; Lin, C. F. Plastic Deformation and Fracture Behaviour of Ti–6Al–4V Alloy Loaded With High Strain Rate Under

  4. Birchwood biochar as partial carbon black replacement in styrene-butadiene rubber composites

    Science.gov (United States)

    Birchwood feedstock was used to make slow pyrolysis biochar that contained 89% carbon and rubber. Composites made from blended fillers of 25/75 biochar/carbon black were equivalent to or superior to their 100% carbo...

  5. Ultrafast spectroscopic studies of the photophysics of phenyl- substituted butadienes in liquids

    Energy Technology Data Exchange (ETDEWEB)

    Hoff, R.L.

    1991-08-01

    The transient absorption decay times of tetraphenylbutadiene (TPB) and tetraphenylmethylbutadiene (TPMB) are measured as a function of solvent viscosity and of probe wavelength. The TPB spectra suggest that after excitation, TPB relaxes to the bottom of the excited state well where it relaxes radiatively to the ground state surface. TPMB transient absorption spectra taken using different probe wavelengths decay on different timescales. 71 refs., 38 figs., 6 tabs.

  6. Synthesis of novel N-, S-substituted-polyhalo-1, 3-butadienes and ...

    Indian Academy of Sciences (India)

    once prior to use. 2.2 Crystal structure determination and refinement. Yellow crystals of compound 8c18 suitable for X-ray diffraction analysis were obtained by slow ... −37 ≤ l ≤ 36. Reflections collected. 24008. Independent reflections. 5444 [Rint = 0.083]. Data/restraints/parameters. 4570/0/334. Goodness of fit indicator.

  7. Reinforcement effect of soy protein/carbohydrate ratio in styrene-butadiene polymer

    Science.gov (United States)

    Soy protein and carbohydrate at different ratios were blended with latex to form composites. The variation of protein to carbohydrate ratio has a sifnificant effect on the composite properties and the results from dynamic mechanical method showed a substantial reinforcement effect. The composites ...

  8. Reinforcement Effect of Alkali Hydrolyzed Wheat Gluten and Starch in Carboxylated Styrene-Butadiene Composites

    Science.gov (United States)

    Wheat gluten (WG) and wheat starch (WS) are the protein and carbohydrate obtained from wheat flours. Wheat gluten is not water soluble or dispersible due to its hydrophobic nature. To prepare wheat gluten dispersions, an alkali hydrolysis reaction was carried out to produce a stable aqueous disper...

  9. ARTICLE Crossed Beams Study on the Dynamics of F Atom Reaction with 1,2-Butadiene

    Science.gov (United States)

    Xiao, Chong-fa; Shen, Guan-lin; Wang, Xiu-yan; Yang, Xue-ming

    2010-12-01

    We have investigated the dynamics of the F+C4H6 reaction using the universal crossed molecular beam method. The C4H5F+H reaction channel was observed in this experiment. Angular resolved time-of-flight spectra have been measured for the C4H5F product. Product angular distributions as well as kinetic energy distributions were determined for this product channel. Experimental results show that the C4H5F product is largely backward scattered with considerable forward scattering signal, relative to the F atom beam direction. This suggests that the reaction channel mainly proceeds via a long-lived complex formation mechanism, with possible contribution from a direct SN2 type mechanism.

  10. Modification of poly(styrene-block-butadiene-block-styrene) [SBS] with phosphorus containing fire retardants

    DEFF Research Database (Denmark)

    Chernyy, Sergey; Ullah, Saif; Jomaas, Grunde

    2015-01-01

    An elaborate survey of the chemical modification methods for endowing highly flammable SBS with increased fire resistant properties by means of chemical modification of the polymer backbone with phosphorus containing fire retardant species is presented. Optimal conditions for free radical additio...... application of the H3PO4 modified SBS as a fire retardant additive for bitumen material, in combination with synergetic melamine species, offered 25% better self-extinguishing properties of such formulation already at a low loading level of the fire retardant components (3.5 wt.%)....

  11. Influence of dispersants on aging and frost elastomeric compositions based on butadiene acrylonitrile rubbers

    Directory of Open Access Journals (Sweden)

    R. M. Dolinskaya

    2016-01-01

    Full Text Available The possibility of use of dispergators of various nature for production of rubber technical products with expanded temperature conditions of operation is studied. It is investigated influences of dispergators of Dispergator FL and INT 159 on properties of rubber mixes for receiving products with high resistance to thermal aging or frost resistance. Research of influence of modifiers was conducted for rubber mixes on the basis of butadienenitrile rubbers synthetic (BNRS-18 and BNRS-28. I’s established that at addition of a dispergator of Dispergator FL the indicator of relative deformatstion of compression (RDC and respectively heat stability of rubbers increases. Introduction to structure of elastomeric composition of a dispergator of INT 159 practically doesn’t influence frost resistance, and Dispergator FL worsens her (the coefficient of frost resistance decreases by 15.4–17.8%. Possibly it is connected with the fact that at the lowered temperatures in the presence of Dispergator FL there is a bigger delay of relaxation processes and decrease in energy of the thermal movement of links of macromolecules of rubbers. It becomes insufficient for overcoming of intermolecular interaction in the modified system and commission of conformational transitions of macromolecules under the influence of external loading. Mechanical energy is to a large extent mentioned not on change of a form of macromolecules, and on their mechanodestruction. However, it increases heat stability since it that is higher, than molecular mobility is lower. INT 159 dispergator components, settling down on borders of supramolecular formations of elastomers, increase mobility of links of macromolecules of rubbers, weaken chemical bonds in them, reduce thermal stability, but at the same time INT 159 dispergator practically doesn’t reduce frost resistance therefore it is expedient to apply it when receiving frost-resistant elastomeric composition. Thus, when receiving thermostable elastomeric compositions it is necessary to use Dispergator FL, and frost-resistant – INT 159 dispergator.

  12. Silyl- and disilanyl-1,3-butadiyne polymers from hexachloro-1,3-butadiene

    Science.gov (United States)

    Barton, T.J.; Ijadi-Maghsoodi, S.

    1990-10-23

    Organosilane polymers having recurring silylene-1,3-butadiyne and/or disilylene-1,3-butadiyne units are prepared in a one-pot synthesis from hexachlorobutadiene. Depending on the organic substituents (R and R[prime]), these polymers have useful film-forming properties, and are converted to the ceramic, silicon carbide upon heating a very uniform high char yields. They can also be pulled into fibers. The polymers are thermally crosslinked above 100 C.

  13. 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.

  14. 21 CFR 177.1020 - Acrylonitrile/butadiene/sty-rene co-polymer.

    Science.gov (United States)

    2010-04-01

    ... percent acetic acid, or n-heptane for 8 days at 120 °F. (2) The finished food-contact article shall yield... water and 3 percent acetic acid at 150 °F for 15 days when analyzed by a polarographic method titled... production. Such adjuvants may include substances generally recognized as safe in food, substances used in...

  15. 21 CFR 177.1030 - Acrylonitrile/butadiene/styrene/methyl methacrylate copolymer.

    Science.gov (United States)

    2010-04-01

    ... acetic acid, 50 percent ethanol, and n-heptane for 10 days at 120 °F. (2) The finished food-contact... to distilled water, 3 percent acetic acid and n-heptane at 190 °F for 2 hours, cooled to 120 °F (80... section may contain adjuvant substances required in its production. Such adjuvants may include substances...

  16. 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.

  17. Penelitian penggunaan campuran karet alam RSS dengan stiren butadien rubber (SBR dalam pembuatan soft rubber lining

    Directory of Open Access Journals (Sweden)

    Penny Setyowati

    1995-06-01

    Full Text Available The objective of this research is to obtain optimum composition of RSS and SBR compound for making soft rubber lining compound. Based on seven combination of trials in compound formulation proved that formulation with composition of RSS 50 parts and SBR 50 parts give the best physical properties and highly cemented on steel by using “Desmodur R” adhesive solution.

  18. Production of Acrylonitrile Butadiene Styrene/High-Density Polyethylene Composites from Waste Sources by Using Coupling Agents

    Science.gov (United States)

    Miskolczi, N.; Szakacs, H.; Sedlarik, V.; Kucharczyk, P.; Riegel, E.

    2014-07-01

    A possible way of recycling plastic wastes has been investigated. Polyalkenyl-poly-maleic-anhydride derivates were synthesized and employed in ABS and HDPE blends to eliminate their immiscibility. By this way, the recycling of ABS and HDPE could be performed with improved mechanical properties of reshaped specimens.

  19. 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.

  20. Graft modification of styrene-butadiene rubber with. gamma. -mercaptpropyltrimethoxysilane. Gamma. -mercaptpropyltrimethoxysilane wo mochiita SBR no graft kaishitsu

    Energy Technology Data Exchange (ETDEWEB)

    Kodama, S.; Kawasaki, H.; Mitsuishi, K.; Nishi, K. (Industrial Technology Center of Okayama, Okayama (Japan))

    1991-08-05

    The method of irradiation to rubber sheet kneaded with {gamma}-MPS (mercaptpropyltrimethoxysilane) is studied as a simple rubber modification method, and the blended effect of silica on the reformed rubber sheet is investigated. Graft modification can be made by using a photo-initiator. The graft efficiency reaches near 90% in nitrogen gas flow with 90 minute irradiation. However, the reaction in air is slow with low graft efficiency, and gelation of rubber is observed. The 300% modulus of the modified vulcanized rubber has comparatively low graft rate which is larger than unreformed one or the one blended with {gamma}-MPS surface reforming silica, and the tear strength, compression permanent deformation, wear resistance, etc. are also improved. The interface adhesive between rubber and filler is better than that in the case where {gamma}-MPS is used as the surface reformer for silica. If the specimen is left at room temperature after irradiation, remarkable gelation is observed. 7 refs., 7 figs., 3 tabs.

  1. Effect of electron beam irradiation on the properties of natural rubber (NR)/styrene-butadiene rubber (SBR) blend

    Energy Technology Data Exchange (ETDEWEB)

    Manshaie, R. [Department of Chemical Engineering, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Nouri Khorasani, S., E-mail: saied@cc.iut.ac.i [Department of Chemical Engineering, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Jahanbani Veshare, S. [Department of Chemical Engineering, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Rezaei Abadchi, M. [Department of Polymer Engineering, Amirkabir University of Technology, Tehran (Iran, Islamic Republic of)

    2011-01-15

    In this study, physico-mechanical properties of NR/SBR blends cured by electron beam irradiation and sulfur were compared. The NR/SBR blends were prepared using a two-roll mill. Electron beam irradiations of 100-400 kGy were applied to cure the blends and changes in physico-mechanical properties were studied as a function of irradiation. Also, oil resistance and the effect of thermal ageing on mechanical properties of the blends were investigated. The results show that the irradiated blends have better mechanical properties than those cured by sulfur system. The irradiation cured samples also exhibited better heat stability than the sulfur cured samples. The blend cured by the highest dose shows the lowest swelling and high oil resistance compared with the other samples cured by irradiation.

  2. Influence of notch depth on tearing morphology and tearing energy in carbon-black-loaded SBR (styrene butadiene rubber)

    Energy Technology Data Exchange (ETDEWEB)

    Goldberg, A.; LeMay, J.D.; Sanchez, R.J.; Stone, J.C.; Patt, J.

    1987-01-30

    Tearing energies (T) have been evaluated for carbon-black-reinforced SBR tested in uniaxial tension. The influence of notch depth on T and fracture morphology have also been determined. The influence of notch depth on the stress-strain behavior and on the failure stress and failure strain is also illustrated. The ratio of recovered-to-input energy as a function of both stress and strain was determined for notched and notch-free samples.

  3. Effect of electron beam irradiation on the properties of natural rubber (NR)/styrene-butadiene rubber (SBR) blend

    Science.gov (United States)

    Manshaie, R.; Nouri Khorasani, S.; Jahanbani Veshare, S.; Rezaei Abadchi, M.

    2011-01-01

    In this study, physico-mechanical properties of NR/SBR blends cured by electron beam irradiation and sulfur were compared. The NR/SBR blends were prepared using a two-roll mill. Electron beam irradiations of 100-400 kGy were applied to cure the blends and changes in physico-mechanical properties were studied as a function of irradiation. Also, oil resistance and the effect of thermal ageing on mechanical properties of the blends were investigated. The results show that the irradiated blends have better mechanical properties than those cured by sulfur system. The irradiation cured samples also exhibited better heat stability than the sulfur cured samples. The blend cured by the highest dose shows the lowest swelling and high oil resistance compared with the other samples cured by irradiation.

  4. Synergistic effect of plasma-modified halloysite nanotubes and carbon black in natural rubber-butadiene rubber blend

    NARCIS (Netherlands)

    Poikelispaa, Minna; Das, Amit; Dierkes, Wilma K.; Vuorinen, Jyrki

    2013-01-01

    Halloysite nanotubes (HNTs) were investigated concerning their suitability for rubber reinforcement. As they have geometrical similarity with carbon nanotubes, they were expected to impart a significant reinforcement effect on the rubber compounds but the dispersion of the nanofillers is difficult.

  5. Reinforcing effect of plasma modified halloysite nanotubes in a carbon black filled natural rubber-butadien rubber matrix

    NARCIS (Netherlands)

    Poikelispaa, Minna; Das, Amit; Dierkes, Wilma K.; Vuorinen, Jyrki

    2011-01-01

    Rubber composites are generally produced by the direct incorporation of fillers like carbon black and/or silica into the rubber matrix. The incorporation of different types of nanofillers is the subject of recent research with the aim of preparing composites with special compositions and properties.

  6. 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. Copyright © 2017 Elsevier Ltd. All rights reserved.

  7. Reinforcement Effect of Alkali-Hydrolyzed Wheat Gluten and Shear-Degraded Wheat Starch in Carboxylated Styrene-Butadiene Composites

    Science.gov (United States)

    Wheat gluten (WG) and wheat starch (WS) are the protein and carbohydrate obtained from wheat flours. Wheat gluten is not water soluble or dispersible due to its hydrophobic nature. To prepare wheat gluten dispersions, an alkali hydrolysis reaction was carried out to produce a stable aqueous disper...

  8. Application of gamma irradiation for incorporation of rubber powder in the formulations of acrylonitrile-butadiene rubber (NBR)

    Energy Technology Data Exchange (ETDEWEB)

    Kiyan, Ludmila Y.P.; Parra, Duclerc Fernandes, E-mail: ludmilapozzo@gmail.com [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Centro de Quimica e Meio Ambiente (CQMA)

    2013-07-01

    Full text: Polymeric materials do not decompose easily, disposal of waste polymers is a major environmental problem of global character. Recycling is an economical alternative and environmentally recommended for polymers consumed and discarded by society. As regards the rubber in object, its natural decomposition is much slower due to their highly crosslinked, in three-dimensional networks, structures which makes it an infusible and insoluble material. Moreover, these three dimensional structures entails several problems for their recovery and reprocessing. The aim of this paper was to study the behavior of NBR rubber recycle. It was used rubber powder from industry. The powder was irradiated in master-batch composition and used directly in classical formulations for rubber vulcanization. The master-batch processed was irradiated at doses of 50, 100 and 150kGy in {sup 60}Co source at 5 kGy s{sup -1} rate, at room temperature. Gamma radiation created active sites during devulcanization that promoted further integration of the rubber powder in formulations for commercial use. The processes were compared and their products were characterized by analytical methods of the physical properties such as tensile strength and elongation. The greatest change in the properties of polymeric materials by exposure to ionizing radiation resulted mainly of two main reactions occurring in the polymer molecule: chains scission (degradation) and crosslinking. Although these two processes occur simultaneously in all the polymers, the predominance of one or other effect depends mainly of the chemical structure of each polymer, and the irradiation conditions. In the results was observed the behavior of nitrile rubber under different doses and radiation improvement of the mechanical properties. (author)

  9. 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.

  10. Preparation, characterization, dielectric properties and diffusion studies of styrene butadiene rubber (SBR)/manganous tungstate (MnWO4) nanocomposites

    Science.gov (United States)

    Jasna, V. C.; Ramesan, M. T.

    2017-06-01

    Nanocomposites based on SBR with different content of manganous tungstate nanoparticles were prepared and characterized by FTIR, UV-visible spectroscopy, XRD, SEM, TGA, DSC and impedance analysis. The interaction between nanoparticles and the elastomer was clear from the shift in peaks of UV and FTIR. XRD and SEM analysis showed the uniform arrangement of nanoparticles in SBR matrix. Glass transition temperature, thermal stability and dielectric properties of composites were enhanced by the addition of nanoparticles. Sorption studies of nanocomposites were done in aromatic solvents at different temperature. Sorption data obtained were used to estimate the thermodynamic properties.

  11. Effects of interfacial interaction on the properties of poly(vinyl chloride)/styrene-butadiene rubber blends

    Science.gov (United States)

    Zhu, Shuihan

    PVC/SBR blends---new thermoplastic elastomer material---were developed. They have potential applications due to low costs and low-temperature elasticity. A unique compatibilization method was employed to enhance the mechanical properties of the materials a compatibilizer miscible with one of the blend components can react chemically with the other component(s). Improvements in tensile and impact behavior were observed as a result of the compatibilization. A novel characterization technique to study the interface of PVC/SBR blends was developed. This technique involves the observation of the unstained sample under electron beam irradiation by a transmission electron microscope (TEM). An enrichment of rubber at the interface between PVC and SBR was detected in the compatiblized PVC/SBR blends. Magnetic relaxation measurements show that the rubber concentration in the proximity of PVC increases with the degree of covulcanization between NBR and SBR. The interface development and the rheological effect during processing were investigated. The interfacial concentration profile and the interfacial thickness were obtained by grayscale measurements on TEM micrographs, evaluation of SIMS images, and measurements of micromechanical properties.

  12. Acrylic acid removal by acrylic acid utilizing bacteria from acrylonitrile-butadiene-styrene resin manufactured wastewater treatment system.

    Science.gov (United States)

    Wang, C C; Lee, C M

    2006-01-01

    The aim of this study is to isolate the acrylic acid utilizing bacteria from the ABS resin manufactured wastewater treatment system. The bacteria should have the ability to remove acrylic acid and tolerate the acrylonitrile and acrylamide toxicity. The aim is also to understand the performance of isolated pure strain for treating different initial acrylic acid concentrations from synthetic wastewater. The results are: twenty strains were isolated from the ABS resin manufactured wastewater treatment system and twelve of them could utilize 600 mg/l acrylic acid for growth. Seven of twelve strains could tolerate the acrylonitrile and acrylamide toxicity, when the concentration was below 300 mg/l. Bacillus thuringiensis was one of the seven strains and the optimum growth temperature was 32 degrees C. Bacillus thuringiensis could utilize acrylic acid for growth, when the initial acrylic acid concentration was below 1,690.4 mg/l. Besides this, when the initial acrylic acid concentration was below 606.8 mg/l, the acrylic acid removal efficiency exceeded 96.3%. Bacillus thuringiensis could tolerate 295.7 mg/l acrylamide and 198.4 mg/l acrylonitrile toxicity but could not tolerate 297.3 mg/l epsilon-caprolactam.

  13. Aggregate structure and effect of phthalic anhydride modified soy protein on the mechanical properties of styrene-butadiene copolymer

    Science.gov (United States)

    The aggregate structure of phthalic anhydride (PA) modified soy protein isolate (SPI) was investigated by estimating its fractal dimension from the equilibrated dynamic strain sweep experiments. The estimated fractal dimensions of the filler aggregates were less than 2, indicating that these partic...

  14. Base-free Pd/TOMPP-Catalyzed Telomerization of 1,3-Butadiene with Carbohydrates and sugar alcohols

    NARCIS (Netherlands)

    Hausoul, P.J.C.|info:eu-repo/dai/nl/313957630; Bruijnincx, P.C.A.|info:eu-repo/dai/nl/33799529X; Klein Gebbink, R.J.M.|info:eu-repo/dai/nl/166032646; Weckhuysen, B.M.|info:eu-repo/dai/nl/285484397

    2009-01-01

    Sugar and alcohol - a superior combo: The telomerization activity of the Pd/TOMPP catalyst is screened using thirteen different biomass-derived carbohydrates and sugar alcohols. High substrate conversions are achieved by using low Pd loading and without the use of an added base. In terms of

  15. 21 CFR 177.1050 - Acrylonitrile/styrene copoly-mer modified with butadiene/styrene elastomer.

    Science.gov (United States)

    2010-04-01

    ... milliliters of 3 percent acetic acid in a Pyrex glass pressure bottle. (3) The pyrex glass pressure bottle is... contain adjuvant substances required in its production. Such adjuvants may include substances generally...

  16. Surface treatment with Fenton for separation of acrylonitrile-butadiene-styrene and polyvinylchloride waste plastics by flotation.

    Science.gov (United States)

    Wang, Jian-Chao; Wang, Hui; Huang, Luo-Luo; Wang, Chong-Qing

    2017-09-01

    Surface treatment with Fenton was applied to flotation separation of acrylonitrile-butadienestyrene (ABS) and polyvinylchloride (PVC). After treatment, the floatability of ABS has a dramatic decrease, while the floatability of PVC is not affected. Fourier transform infrared spectroscopy (FT-IR) spectra and X-ray photoelectron spectroscopy (XPS) spectra were recorded to ascertain the mechanism of Fenton treatment. FT-IR and XPS analysis confirms that the introduction of oxygen-containing group occurs on the surface of ABS. The optimum conditions are molar ration (H 2 O 2 :Fe 2+ ) 10000, H 2 O 2 concentration 0.4M/L, pH 5.8, treatment time 2min and temperature 25°C, frother concentration 15mg/L and flotation time 3min. Particle sizes and mixing ratios were also investigated. Plastic mixtures of ABS and PVC with different particle sizes and mixing ratios can be effectively separated. The purity of ABS and PVC are up to 100% and 99.78%, respectively; the recovery of ABS and PVC are up to 99.89% and 100%, respectively. A practical, environmentally friendly and effective reagent, namely Fenton, was originally applied to surface treatment of ABS and PVC waste plastics for flotation separation of their mixtures. Copyright © 2017 Elsevier Ltd. All rights reserved.

  17. 21 CFR 175.125 - Pressure-sensitive adhesives.

    Science.gov (United States)

    2010-04-01

    .... Butadiene-acrylonitrile copolymer. Butadiene-acrylonitrile-styrene copolymer. Butadiene-styrene copolymer.... Isobutylene-styrene copolymer. Petrolatum. Polybutene-1. Polybutene, hydrogenated; complying with the identity... contain not more than 1 percent by weight of triisopropanolamine). (c) Acrylonitrile copolymers identified...

  18. A DFT study on the aldol condensation reaction on MgO in the process of ethanol to 1,3-butadiene: understanding the structure-activity relationship.

    Science.gov (United States)

    Fan, Dan; Dong, Xiuqin; Yu, Yingzhe; Zhang, Minhua

    2017-09-27

    Using periodic density functional theory calculations, the aldol condensation of acetaldehyde to 3-hydroxybutanal over dehydroxylated MgO surfaces with and without structure defects was investigated. Compared with the C-C coupling step, the enolization step via proton transfer of the α-hydrogen of acetaldehyde to the MgO surface or the proton back-transfer step to form the desired 3-hydroxybutanal has a higher energy barrier, indicating that the proton transfer process is the key step for the aldol condensation on MgO. To highlight the effect of water, we also calculated the proton transfer steps in the presence of water and studied the reaction pathways over the partially hydroxylated MgO surface. The results show that water can participate in the proton back-transfer step by donating a proton to the alkoxide anion to form the 3-hydroxybutanal, thus reducing the activation energy; the surface OH groups induce a lowering of the activation energy barriers for the overall reaction. The results of the electronic structure analysis indicate that a strong Lewis acid-weak/medium base pair may have the best performance for aldol condensation, such as Mg3C-O4C-D produced by divacancy defects and Mg4C-O2CH produced by the dissociative adsorption of water. A strong Lewis acid generated by low-coordinated Mg2+ can adsorb and stabilize the acetaldehyde molecule near the catalyst surface which is beneficial for the abstraction of an α-proton from an acetaldehyde molecule, and a medium or weak Brønsted base is favorable for the proton back-transfer step.

  19. On the molecular structures of the prevailing anti conformers of gaseous cis-1 and trans-1-chloro-1,3-butadiene

    Science.gov (United States)

    Gundersen, Grete; Thomassen, Hanne G.; Boggs, James E.; Collins, Michael L.

    1989-10-01

    The molecular structures of the title compounds have been investigated by ab initio MO calculations and by analyses of room-temperature electron diffraction data alone, as well as by conjoint use of these data and literature ground-state rotational constants of eleven isotopic species. Models for the structures were specified in terms of geometrically consistent rα-parameters under the assumption of Cs molecular symmetry. Literature molecular force fields were used to calculate vibrational amplitude parameter quantities needed for vibrational corrections and for making the three methods compatible. Results of the computed structures were incorporated into the structure analyses so as to reduce the geometry-defining variables for the hydrogen positions from ten to four, and ultimately to constrain the difference parameter Δ a(CC) = ra(C 1C 2) - ra (C 3C 4), to 0.37 and 0.40 pm respectively for the cis and trans isomer. The final structures obtained by conjoint consideration of computational, electron diffraction and spectroscopic evidence then have the following principal distances ( ra in pm) and angle (∠C α in degrees) with estimated standard deviations in parentheses: the cis isomer, r(C 1C 2) = 134.2(2), r(C 3C 4) = 134.5(2), r(C 2C 3) = 146.6(3), r(C-Cl) = 173.0(2), ∠C 1C 2C 3 = 125.5(2), ∠C 4C 3C 2 = 122.3(4), ∠C 2C 1Cl = 123.9(2); the trans isomer, r(C 1C 2) = 134.0(2), r(C 3C 4) = 134.4(2), r(C 2C 3) = 146.1(3), r(CCl) = 172.8(2), ∠C 1C 2C 3 = 122.5(4), ∠C 4C 3C 2 = 123.3(3), ∠C 2C 1Cl = 122.5(2). It is shown that the computational results and the GED structures are not in conflict with the rotational constants used to obtain the literature rs-structures which are however not in good agreement with the present results.

  20. Sifat fisika dan analisis gugus fungsi karet seal o-ring dari bahan termoplastik elastomer nitrile butadiene rubber (NBR) dan polyvinyl chloride (PVC)

    OpenAIRE

    Arum Yuniari; Nursamsi Sarengat

    2013-01-01

    The purpose of this research was to determine the physical properties and functional groups on O-ring rubber seals made of thermoplastic elastomers blend NBR and PVC. Composition of the NBR / PVC were successively varied : 90/10; 85/15; 80/20; 75/25; 70/30 and 65/35 phr. Mixing process between NBR/PVC with additive used a two roll mill within a temperature of 60º - 80 ºC, the vulcanization process used a hydraulic press at a temperature of 170 oC and pressure of 150 kg/cm2. The...

  1. Sifat Fisika Dan Analisis Gugus Fungsi Karet Seal O-ring Dari Bahan Termoplastik Elastomer Nitrile Butadiene Rubber (NBR) Dan Polyvinyl Chloride (PVC)

    OpenAIRE

    Yuniari, Arum; Sarengat, Nursamsi

    2013-01-01

    The purpose of this research was to determine the physical properties and functionalgroups on O-ring rubber seals made of thermoplastic elastomers blend NBR and PVC.Composition of the NBR / PVC were successively varied : 90/10; 85/15; 80/20; 75/25; 70/30 and65/35 phr. Mixing process between NBR/PVC with additive used a two roll mill within atemperature of 60º - 80 ºC, the vulcanization process used a hydraulic press at a temperature of170 oC and pressure of 150 kg/cm2. The physical properties...

  2. The vibrational structure of (E,E’)-1,4-diphenyl-1,3-butadiene. Linear dichroism FTIR spectroscopy and quantum chemical calculations

    DEFF Research Database (Denmark)

    Hansen, Bjarke Knud Vilster; Møller, Søren; Spanget-Larsen, Jens

    2006-01-01

    The title compound (DPB) was investigated by FTIR spectroscopy in liquid solutions and by FTIR linear dichroism (LD) measurements on samples aligned in stretched polyethylene. The LD data provided experimental assignments of molecular transition moment directions and vibrational symmetries for more...... of a nearly complete assignment of the IR active fundamentals of DPB, involving reassignment of a number of transitions. In addition, previously published Raman spectra of DPB were well predicted by the B3LYP/cc-pVTZ calculations....

  3. Plant Growth and Water Purification of Porous Vegetation Concrete Formed of Blast Furnace Slag, Natural Jute Fiber and Styrene Butadiene Latex

    Directory of Open Access Journals (Sweden)

    Hwang-Hee Kim

    2016-04-01

    Full Text Available The purpose of this study is to investigate porous vegetation concrete formed using the industrial by-products blast furnace slag powder and blast furnace slag aggregates. We investigated the void ratio, compressive strength, freeze–thaw resistance, plant growth and water purification properties using concretes containing these by-products, natural jute fiber and latex. The target performance was a compressive strength of ≥12 MPa, a void ratio of ≥25% and a residual compressive strength of ≥80% following 100 freeze–thaw cycles. Using these target performance metrics and test results for plant growth and water purification, an optimal mixing ratio was identified. The study characterized the physical and mechanical properties of the optimal mix, and found that the compressive strength decreased compared with the default mix, but that the void ratio and the freeze–thaw resistance increased. When latex was used, the compressive strength, void ratio and freeze–thaw resistance all improved, satisfying the target performance metrics. Vegetation growth tests showed that plant growth was more active when the blast furnace slag aggregate was used. Furthermore, the use of latex was also found to promote vegetation growth, which is attributed to the latex forming a film coating that suppresses leaching of toxic components from the cement. Water purification tests showed no so significant differences between different mixing ratios; however, a comparison of mixes with and without vegetation indicated improved water purification in terms of the total phosphorus content when vegetation had been allowed to grow.

  4. EPR Spectroscopy of catalytic systems based on nickel complexes of 1,4-diaza-1,3-butadiene (α-diimine) ligands in hydrogenation and polymerization reactions

    Science.gov (United States)

    Titova, Yu. Yu.; Belykh, L. B.; Schmidt, F. K.

    2015-01-01

    EPR spectroscopy is used to study catalytic hydration and polymerization reaction systems based on α-diimine complexes of Ni(0) and Ni(II) with the general formula NiBr2(DAD-R) (R = -C3H7 or -CH3) or Ni(DAD-CH3)2 (DAD(-C3H7) = 1,4-bis(2,6-diiso-propylphenyl)-2,3-(dimethyl-1,4-diazabuta-1,3-diene, DAD(-CH3) = 1,4-bis(2,6-dimethylphenyl)-2,3-dimethyl-1,4-diazabuta-1,3-diene)), in combination with Lewis acids (AlEt3, AlEt2Cl, AlEtCl2, B(F5C6)3, BF3.OEt2). Ni(I) complexes of the form (DAD-R)NiX2AlX'y(C2H5)3-y composition (an aluminum atom can be replaced by a boron atom) were identified, where R = -CH3 or -C3H7, X = Br, and X' = Cl or -C2H5 and α-diimine anion radicals are included in derivatives of aluminum or boron. Oxidation reactions of the Ni(DAD-CH3)2 complex with aluminum alkyl halides and boron derivatives with formation of paramagnetic nickel complexes are observed. It is found that there is no direct relationship between the polymerization activity of ethylene or hydration of the alkenes and the concentration of paramagnetic particles.

  5. DFT studies of the effectiveness of p-substituted diphenyl amine antioxidants in styrene-butadiene rubber through their Cu(II) coordination ability

    Science.gov (United States)

    Puškárová, Ingrid; Breza, Martin

    2017-07-01

    Structures of a series of diphenyl amine (DPA) antioxidants and of their complexes with Cu2+ were optimized at B3LYP level of theory. DPAs may be divided into two groups according to their molar antioxidant effectiveness (AEM). The effectiveness of high-AEM DPA antioxidants at 130 °C rises with decreasing spin densities at Cu atoms and with the increasing electron density Laplacian at Cu-N bond critical points in the 2[DPA…Cu]2+ complexes similarly as in the case of p-phenylene diamine antioxidants. No such trends are observed at 25 °C and for low- AEM DPA antioxidants.

  6. Sifat fisika dan analisis gugus fungsi karet seal o-ring dari bahan termoplastik elastomer nitrile butadiene rubber (NBR dan polyvinyl chloride (PVC

    Directory of Open Access Journals (Sweden)

    Arum Yuniari

    2013-06-01

    Full Text Available The purpose of this research was to determine the physical properties and functional groups on O-ring rubber seals made of thermoplastic elastomers blend NBR and PVC. Composition of the NBR / PVC were successively varied : 90/10; 85/15; 80/20; 75/25; 70/30 and 65/35 phr. Mixing process between NBR/PVC with additive used a two roll mill within a temperature of 60º - 80 ºC, the vulcanization process used a hydraulic press at a temperature of 170 oC and pressure of 150 kg/cm2. The physical properties were evaluated including tensile strength, elongation at break, hardness, before and after aging, hardness after immersion in isooctane and swelling while analysis of functional groups was also carried out by method of Fourier Transform Infrared Spectrophotometer (FTIR. The result of the best vulcanized was characterized by tensile strength 188.93 kg/cm2, the change of tensile strength after aging 2.50%, elongation at break of 400%, the change of elongation at break after aging was 12.5%, hardness 75 shore A, the change of hardness after aging 0%, the change of hardness after immersion in isooctane 1.3%, swelling 0.8% and functional group of vulcanisate was indicated by new peak (OH at wave band of 3468 cm-1. Those formula met the requirements of the technical specifications of ASTM D 2000 seal O-ring.

  7. 40 CFR 721.6900 - Polymer of bisphenol A di-glyc-i-dal ether, substituted al-kenes, and but-a-diene.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Polymer of bisphenol A di-glyc-i-dal... SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.6900 Polymer of bisphenol A di-glyc-i... subject to reporting. (1) The chemical substances identified generically as polymer of bisphenol A...

  8. Mechanical Properties and Vulcanization Characteristics of Styrene-Butadiene Rubber (sbr) Based Compounds Filled with Eggshell Powder as a Bio-Filler

    Science.gov (United States)

    Saeb, Mohammad Reza; Dakhel, Hadi Ramezani; Ghaffari, Akbar

    2008-08-01

    Egg shell is an ordered bioceramic composite with five different layers [1, 2]. In this study, the effect of using various types of eggshell powder including after and before hatching eggshell and boiled eggshell on the mechanical properties and vulcanization characteristics of SBR compounds has been investigated. The obtained results were compared with calcium carbonate filled compounds. Evaluation of mechanical properties exhibited that incorporation of eggshell increased almost all of the mechanical properties of the compounds. BET test demonstrated higher specific area of eggshell powders compare with calcium carbonate. Some of the observed results attributed to higher specific area of eggshell powder. However, there is no definitive reason for some other results at this time. Vulcanization characteristics of the compounds showed that incorporation of eggshell powder had no considerable effect on curing time. The results of this research showed that all kinds of eggshell powders can be used in SBR based compounds successfully.

  9. Effet des Plastifiants sur la Temperature de Transition Vitreuse, Tg, du Butadiene a Terminaison Hydroxy et du Polyazoture de Glycidyle - Simulations et Experiences (Effect of the Plasticizers on the Vitreous Transition Temperature, Tg, of the Butadiene to Termination Hydroxy and the Polyazoture of Glycidyle - Simulations and Experiences)

    Science.gov (United States)

    2008-09-01

    informatique de Puniversite Laval de leur soutien precieux sur le plan informatique , ainsi que les autres membres du centre de bio- informatique . Viii DRDC...Materials Studio de Accelrys Inc., installe sur un ordinateur SGI Altix 3000 du Centre de calcul bio- informatique de l’Universite Laval. Le champ de

  10. Development of bio-based polymers for use in asphalt.

    Science.gov (United States)

    2014-02-01

    Asphalt binder is typically modified with poly type (styrene-butadiene-styrene or SBS) polymers to improve its rheological properties and performance grade. The elastic and principal component of SBS polymers is butadiene. For the last decade, butadi...

  11. Ex Situ and Operando Studies on the Role of Copper in Cu-Promoted SiO2-MgO Catalysts for the Lebedev Ethanol-to-Butadiene Process

    NARCIS (Netherlands)

    Angelici, Carlo; Meirer, Florian; van der Eerden, Ad M. J.; Schaink, Herrick L.; Goryachev, Andrey; Hofmann, Jan P.; Hensen, Emiel J. M.; Weckhuysen, Bert M.; Bruijnincx, Pieter C. A.

    2015-01-01

    Dehydrogenation promoters greatly enhance the performance of SiO2-MgO catalysts in the Lebedev process. Here, the effect of preparation method and order of addition of Cu on the structure and performance of Cu-promoted SiO2-MgO materials is detailed. Addition of Cu to MgO via incipient wetness

  12. Elastomer Suitable for Track Pad Use that will Change from the Amorphous to the Crystalline State on Stress Application

    Science.gov (United States)

    1986-06-08

    Ziegler-Nata polymerizations of: * cis and trans isoprene * cis and trans butadiene * piperylene (1,3 pentadiene) o myrcene (2 methyl-6-methylene-2,7...been reported by Corish’. A tire tread compound with solution polymerized styrene-butadiene copolymers that have a relatively high 1,2 butadiene content...groups: 1) mechanical blends with low MW crystals, 2) mechanical blends with polymeric materials, 3) solution blends with low MW crystals and, 4) solution

  13. Federal Specification MMM-A-1617B for Adhesive, Rubber-Base, General-Purpose HAP-Free Replacement

    Science.gov (United States)

    2011-05-01

    classified into three types (3): • Type I: Non-oil-resistant natural rubber base, synthetic natural (polyisoprene), styrene butadiene (SBR), reclaim...or combinations. • Type II: Oil-resistant polychloroprene rubber base. • Type III: Fuel-resistant butadiene acrylonitrile (nitrile) rubber base...all contained a nitrile polymer base, also known as acrylonitrile butadiene . Nitrile has good resistance to oil, water, and heat. The adhesive

  14. Pengaruh Penambahan SBR Bervariasi Pada Perapat Pintu Air

    OpenAIRE

    pramono, Pramono; Musthofa, Hadi

    1994-01-01

    The aim of research is to find out the effect of styrene butadiene rubber used to the tensile strength, compression set, and the Hardness of the seal. The variation of styrene butadiene rubber are 20, 30 and 40 phr; Statistical analysis Paint out that there is signify difference often tensile strength but unsignify difference at the compression set and hardness.

  15. Pengaruh penambahan SBR bervariasi pada perapat pintu air

    Directory of Open Access Journals (Sweden)

    Pramono Pramono

    1994-04-01

    Full Text Available The aim of research is to find out the effect of styrene butadiene rubber used to the tensile strength, compression set, and the Hardness of the seal. The variation of styrene butadiene rubber are 20, 30 and 40 phr; Statistical analysis Paint out that there is signify difference often tensile strength but unsignify difference at the compression set and hardness.

  16. Kinetics of the thermal decomposition of tetramethylsilane behind ...

    Indian Academy of Sciences (India)

    equal concentrations via reaction 1. It was further con- firmed that, 1,3-butadiene does not decompose in the investigated range of the temperatures, by carrying out its decomposition independently. Skinner et al.,37 and. Hidaka et al.,38 also have reported that 1,3-butadiene does not decompose in this temperature range.

  17. Importance of fullerenic active sites in surface modification of carbon black by plasma polymerisation

    NARCIS (Netherlands)

    Mathew, T.; Datta, Rabin; Dierkes, Wilma K.; Ooij, W.J.; Noordermeer, Jacobus W.M.; Probst, N.; Gruenberger, T.M.; Probst, N.

    2009-01-01

    Carbon black is widely used as an active filler in rubber to improve the physical properties. The surface energy of carbon black is high compared to that of various elastomers like Styrene–Butadiene rubber, Butadiene rubber and Ethylene–Propylene Diene rubber. Reducing the surface energy and

  18. 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

    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

  19. Effect of shearing on the reinforcement properties of vital wheat gluten

    Science.gov (United States)

    The reinforcement properties of vital wheat gluten as a biomaterial filler for a carboxylated styrene-butadiene rubber were examined to assess its effectiveness as a filler for carboxylated styrene-butadiene rubber composites. Composites were formulated using 10-40% vital wheat gluten by mixing aqu...

  20. 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...3 using a FORTUS three-dimensional (3-D) printer using polycarbonate and acrylonitrile butadiene styrene (PC-ABS) plastic. After all of the pieces

  1. 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

  2. to view fulltext PDF

    Indian Academy of Sciences (India)

    1, 3-butadiene. Synthesis of novel N-, S-substituted-polyhalo-1, 3- butadienes and crystal structure of dibutadienyl homo- piperazine. 755. 1-3-diaminopropane. Synthesis and evaluation of some novel precursors of oxazolidinone analogues of chloroquinoline for their antimicrobial and cytotoxic potential. 1093.

  3. Abstracts. 1978 AFOSR Contractors Meeting on Air-Breathing Combustion Dynamics and Kinetics, Ramada Inn-Downtown Dayton, Ohio, 10 - 13 October 1978

    Science.gov (United States)

    1978-10-13

    Advanced Diagnostic Techniques 9:30 45 Laser Induced Fluorescence Spec- J.W. Daily troscopy for Species Concentration Univ. of California/Berkeley...selected physical properties. The generic polymers that were evaluated included: acrylonitrile butadiene styrene, bisphenol A polycarbonate, 9,9 bis...rated as follows, in order of increased fire safety: polyphenylene oxide; acrylonitrile butadiene styrene; bisphenol A polycarbonate; chlorinated

  4. Polar Diels-Alder reactions using electrophilic nitrobenzothiophenes. A combined experimental and DFT study

    Science.gov (United States)

    Della Rosa, Claudia D.; Mancini, Pedro M. E.; Kneeteman, Maria N.; Lopez Baena, Anna F.; Suligoy, Melisa A.; Domingo, Luis R.

    2015-01-01

    The reactions between 2- and 3-nitrobenzothiophenes with three dienes of different nucleophilicity, 1-methoxy-3-trimethylsilyloxy-1,3-butadiene, 1-trimethylsilyloxy-1,3-butadiene and isoprene developed in anhydrous benzene and alternative under microwave irradiation with molecular solvents or in free solvent conditions, respectively, for produce dibenzothiophenes permit to conclude that both nitroheterocycles act as electrophile with the cited dienes. In the cases of the dienes 1-methoxy-3-trimethylsilyloxy-1,3-butadiene and 1-trimethylsilyloxy-1,3-butadiene which posses major nucleophilicity the observed product is the normal cycloaddition one. However when the diene is isoprene the product with both electrophiles follow the hetero Diels-Alder way. These reactions are considered polar cycloaddition reactions and the yields are reasonables. Moreover the polar Diels-Alder reactions of nitrobenzothiophenes with electron rich dienes 1-trimethylsilyloxy-1,3-butadiene have been theoretically studied using DFT methods.

  5. Polimerização 1,4 - cis de butadieno com o sistema catalítico tetracloreto de titânio/triisobutilalumínio/iodo 1,4 cis-Polymerization of butadiene by the catalyst system titanium tetrachloride/triisobutylaluminium/iodine

    Directory of Open Access Journals (Sweden)

    Neusa M. T. Pires

    2000-12-01

    Full Text Available Foi utilizado o sistema catalítico tipo Ziegler-Natta modificado, constituído por TiCl4/I2/Al(i-Bu3 para a síntese de polibutadieno com alto teor de unidades 1,4-cis. Foi estudada a influência da variação da composição do sistema catalítico e da temperatura reacional na atividade catalítica, no massa molar e na microestrutura do polibutadieno. Os polímeros foram caracterizados por espectroscopia na região do infravermelho, cromatografia por exclusão por tamanho e calorimetria diferencial de varredura. Foi obtido polibutadieno com até 92% de unidades 1,4-cis e baixo teor de gel. A massa molar ponderal média variou, com a composição do sistema catalítico e com a temperatura reacional, na faixa de 3 a 50 x 10(4 e a polidispersão variou na faixa de 1,8 a 3,3. A atividade catalítica máxima foi obtida para as razões molares Al/Ti = 5 e I2/Ti = 2.A modified Ziegler-Natta type catalytic system consisting of TiCl4/I2/Al(i-Bu3 was used to produce polybutadiene with high content of 1,4-cis repeating units. The influence of the catalytic system composition and temperature on the catalyst activity, molecular weight and microstructure of the polybutadiene was studied. The polymers were characterized by infrared spectroscopy and size exclusion chromatography. Polybutadiene with up to 92% of 1,4-cis repeating units and low gel content was produced. The polymer molecular weight was dependent on the catalytic system composition and reaction temperature. The weight-average molecular weight varied from 3 to 50 x 10(4; the molecular weight distribution was low, ranging, from 1.8 to 3.3. The maximum catalytic activity was achieved at molar ratios Al/Ti = 5 and I2/Ti = 2.

  6. The evaluation of tetrabutylamonium bis(4-ethylphenylsulphonyldithiocarbimate)zincate(II) (ZNIBU) efficiency as a reclaiming agent for styrene-butadiene rubber (SBR); Avalicao da eficiencia do bis(4-metilfenilsulfonilditiocarbimato)zincato(II) de tetrabutilamonio (ZNIBU) como agente de regeneracao para borracha de butadieno-estireno (SBR)

    Energy Technology Data Exchange (ETDEWEB)

    Moreno, Pedro H.H.; Visconte, Leila L.Y.; Pacheco, Elen B.A.V., E-mail: pedro_hhm@ima.ufrj.br [Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ (Brazil); Tavares, Eder C. [Universidade Federal de Itajuba (UNIFEI), Itajuba, MG (Brazil)

    2015-07-01

    In recent years, the production of rubber waste has been reported as a serious environmental problem. The chemical structure of rubbers (crosslinked, insoluble and infusible polymers) makes its reprocessing very difficult, unlike thermoplastics. The most common methods to treat rubber waste are of thermal, mechanical and chemical nature, wherein the chemical methods the purpose is to regenerate the rubber. Early studies with tetrabutylamonium bis(4-methylphenylsulphonyldithiocarbimate)zincate(II) (ZNIBU) point to its ability as an accelerator in the rubber curing process. In this work, this zinc complex was evaluated as a chemical regeneration agent. ZNIBU was synthesized and characterized by Nuclear Magnetic Resonance ({sup 13}C NMR) and Fourier Transform Infrared Spectroscopy (FTIR). The mixture of virgin SBR with vulcanization ingredients was performed in a two-roll mill, and the composition was then vulcanized and molded on a hydraulic press. The synthesized ZNIBU was then mixed with the vulcanized rubber and devulcanization was observed. Finally, the devulcanized elastomeric composition was revulcanized. The revulcanization of SBR regenerated with ZNIBU led to the formation of a rubber with maximum torque near the maximum torque of the virgin vulcanized rubber. After adjusting the optimal conditions of regeneration, mechanical tests will be carried out (tensile strength, tear strength and hardness) for the specimens of both vulcanized and revulcanized rubbers in order to compare their mechanical properties. (author)

  7. 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.

  8. Polymer Coating of Carbon Nanotube Fibers for Electric Microcables

    National Research Council Canada - National Science Library

    Alvarez, Noe; Ochmann, Timothy; Kienzle, Nicholas; Ruff, Brad; Haase, Mark; Hopkins, Tracy; Pixley, Sarah; Mast, David; Schulz, Mark; Shanov, Vesselin

    2014-01-01

    .... Ideally, a flexible insulator such as hydrogenated nitrile butadiene rubber (HNBR) on the CNT fiber can allow fabrication of CNT coils that can be assembled into lightweight, corrosion resistant...

  9. A novel method for recovery of acidic sludge of used-motor oil reprocessing industries to bitumen using bentonite and SBS

    National Research Council Canada - National Science Library

    Ahmad Jonidi Jafari; malek hassanpour; Mitra Gholam; Mehdi Farzadkia

    2014-01-01

    .... The acidic sludge contains unsaturated compounds that are polar and asphaltene. The bitumen under certain conditions is produced from mixing of bentonite, polymer styrene – butadiene – styrene (SBS), and acidic sludge...

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

    National Research Council Canada - National Science Library

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

    2014-01-01

    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...

  11. STUDY OF TECHNICAL AND TECHNOLOGICAL PROPERTIES STIROTEP-65

    Directory of Open Access Journals (Sweden)

    V. A. Sedyh

    2013-01-01

    Full Text Available Elastic-strength properties and rheology of the styrene-butadiene block copolymer StiroTEP-65 were studied. In order to expand the sphere of application StiroTEP-65 studied its compatibility with PMMA.

  12. Investigation of the use of recycled polymer-modified asphalt in asphaltic concrete pavements.

    Science.gov (United States)

    2004-06-30

    This report presents issues associated with recycling polymer modified asphalt cements (PMACs), particularly blending aged PMAC with new PMAC. A styrene-butadiene-styrene (SBS) PMAC was selected and graded using the Superpave Performance Grading (PG)...

  13. 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.

  14. SUPPLEMENTARY INFORMATION REGULAR ARTICLE ...

    Indian Academy of Sciences (India)

    butadiene: A DFT study. SAFA ALI-ASGARI[1], JAFAR IZADI NIA and SAMIRA ZALI. Department of Chemistry, Shahrood Branch, Islamic Azad University, Shahrood, Iran. E-mail: safa1308@yahoo.com; s_aliasgari@iau-shahrood.ac.ir.

  15. Investigation to Identify Performance Criteria and Test Methods for Evaluating Single-Ply Roofing Systems.

    Science.gov (United States)

    1987-03-01

    compounded from PVC, butadiene- acrylonitrile copolymers, nonvolatile polymeric plasticizers, and other proprietary ingredients. The membranes usually...carbon arc weatherometer, fluorescent UV-condensation apparatus, South Florida direct inland weathering, and the Equatorial Mount With Mirrors for

  16. Acta Aeronautica et Astronautica Sinica (Selected Articles),

    Science.gov (United States)

    1984-01-30

    Using the diglycidyl ether of biphenol A--butadiene-acrylo- nitrile rubber with random carboxyl groups--2-ethyl-4-methylimi- dazol epoxy resin system as...4 The results of the study showed that after being modified by butadiene rubber with a random carboxyl group and biphenol A, the fracture surface...energy of the biphenol A epoxy resin was increased by 1-4 times. The 106 impact strength was increased by 2-10 times. The toughness modu- lus (the area

  17. Perbandingan Sifat Mekanik Fisik Vulkanisat Sbr Dan Sbr/nr Menggunakan Bahan Pengisi Pati Termodifikasi Resorcinol Formaldehyde

    OpenAIRE

    Susanto, Tri

    2016-01-01

    Penelitian ini bertujuan untuk mengetahui perbandingan karakteristik vulkanisat komposit Styrene Butadiene Rubber (SBR) dan campuran Styrene Butadiene Rubber dan Natural Rubber (SBR/NR) yang keduanya menggunakan bahan pengisi starch (pati) termodifikasi Resorcinol Formaldehyde (SRF) sebagai bahan substituen Carbon Black (CB). Rasio CB/SRF untuk tiap vulkanisat yang digunakan berturut-turut 60/0; 55/5; 50/10; 45/15; 40/20 phr. Pengamatan dilakukan dengan menguji sifat physco-mechanic vulkanisa...

  18. Growth of Fullerene Fragments Using the Diels-Alder Cycloaddition Reaction: First Step towards a C60 Synthesis by Dimerization

    Directory of Open Access Journals (Sweden)

    Julio A. Alonso

    2013-02-01

    Full Text Available Density Functional Theory has been used to model the Diels-Alder reactions of the fullerene fragments triindenetriphenilene and pentacyclopentacorannulene with ethylene and 1,3-butadiene. The purpose is to prove the feasibility of using Diels-Alder cycloaddition reactions to grow fullerene fragments step by step, and to dimerize fullerene fragments, as a way to obtain C60. The dienophile character of the fullerene fragments is dominant, and the reaction of butadiene with pentacyclopentacorannulene is favored.

  19. Compatibility Studies on Elastomers and Polymers with Ethanol Blended Gasoline

    OpenAIRE

    Dhaliwal, J S; M. S. Negi; G. S. Kapur; Shashi Kant

    2014-01-01

    This paper reports the compatibility studies of 10% ethanol blended gasoline (E10) with four types of elastomer materials, namely, Neoprene rubber, Nitrile rubber, hydrogenated Nitrile butadiene rubber (HNBR), and Polyvinyl chloride/Nitrile butadiene rubber blend (PVC/NBR), and two types of plastic materials, namely, Nylon-66 and Polyoxymethylene (Delrin). These materials have applications in automotives as engine seals, gaskets, fuel system seals and hoses, and so forth. Two types of the eth...

  20. Growth of fullerene fragments using the Diels-Alder cycloaddition reaction: first step towards a C60 synthesis by dimerization.

    Science.gov (United States)

    Mojica, Martha; Méndez, Francisco; Alonso, Julio A

    2013-02-13

    Density Functional Theory has been used to model the Diels-Alder reactions of the fullerene fragments triindenetriphenilene and pentacyclopentacorannulene with ethylene and 1,3-butadiene. The purpose is to prove the feasibility of using Diels-Alder cycloaddition reactions to grow fullerene fragments step by step, and to dimerize fullerene fragments, as a way to obtain C₆₀. The dienophile character of the fullerene fragments is dominant, and the reaction of butadiene with pentacyclopentacorannulene is favored.

  1. Melt processing and property testing of a model system of plastics contained in waste from electrical and electronic equipment.

    Science.gov (United States)

    Triantou, Marianna I; Tarantili, Petroula A; Andreopoulos, Andreas G

    2015-05-01

    In the present research, blending of polymers used in electrical and electronic equipment, i.e. acrylonitrile-butadiene-styrene terpolymer, polycarbonate and polypropylene, was performed in a twin-screw extruder, in order to explore the effect process parameters on the mixture properties, in an attempt to determine some characteristics of a fast and economical procedure for waste management. The addition of polycarbonate in acrylonitrile-butadiene-styrene terpolymer seemed to increase its thermal stability. Also, the addition of polypropylene in acrylonitrile-butadiene-styrene terpolymer facilitates its melt processing, whereas the addition of acrylonitrile-butadiene-styrene terpolymer in polypropylene improves its mechanical performance. Moreover, the upgrading of the above blends by incorporating 2 phr organically modified montmorillonite was investigated. The prepared nanocomposites exhibit greater tensile strength, elastic modulus and storage modulus, as well as higher melt viscosity, compared with the unreinforced blends. The incorporation of montmorillonite nanoplatelets in polycarbonate-rich acrylonitrile-butadiene-styrene terpolymer/polycarbonate blends turns the thermal degradation mechanism into a two-stage process. Alternatively to mechanical recycling, the energy recovery from the combustion of acrylonitrile-butadiene-styrene terpolymer/polycarbonate and acrylonitrile-butadiene-styrene terpolymer/polypropylene blends was recorded by measuring the gross calorific value. Comparing the investigated polymers, polypropylene presents the higher gross calorific value, followed by acrylonitrile-butadiene-styrene terpolymer and then polycarbonate. The above study allows a rough comparative evaluation of various methodologies for treating plastics from waste from electrical and electronic equipment. © The Author(s) 2015.

  2. 2,3-Bis{[2,3-dimethyl-6-(phenyl-vin-yl)phen-yl]imino}-butane.

    Science.gov (United States)

    Zhao, Jie; Yuan, Jianchao; Xu, Weibing; Chen, Jingjing; Mu, Yanqiong

    2014-02-01

    In the title compound, C36H36N2, a product of the condensation reaction of 2,3-dimethyl-6-phenyl-vinyl-benzenamine and 2,3-butane-dione, the complete mol-ecule is generated by the application of an inversion centre. The central C-C bond in the 1,4-di-aza-butadiene fragment is trans-configured and situated about the inversion center. The dihedral angle between the ring attached to N and the 1,4-di-aza-butadiene plane is 78.24 (36)°, while the 1,4-di-aza-butadiene plane makes an angle of 30.71 (26)° with the phenyl ring.

  3. Exploring Reaction Mechanism on Generalized Force Modified Potential Energy Surfaces (G-FMPES) for Diels-Alder Reaction

    Science.gov (United States)

    Jha, Sanjiv; Brown, Katie; Subramanian, Gopinath

    We apply a recent formulation for searching minimum energy reaction path (MERP) and saddle point to atomic systems subjected to an external force. We demonstrate the effect of a loading modality resembling hydrostatic pressure on the trans to cis conformational change of 1,3-butadiene, and the simplest Diels-Alder reaction between ethylene and 1,3-butadiene. The calculated MERP and saddle points on the generalized force modified potential energy surface (G-FMPES) are compared with the corresponding quantities on an unmodified potential energy surface. Our study is performed using electronic structure calculations at the HF/6-31G** level as implemented in the AIMS-MOLPRO code. Our calculations suggest that the added compressive pressure lowers the energy of cis butadiene. The activation energy barrier for the concerted Diels-Alder reaction is found to decrease progressively with increasing compressive pressure.

  4. Upgrading of lignocellulosic biorefinery to value-added chemicals: Sustainability and economics of bioethanol-derivatives

    DEFF Research Database (Denmark)

    Cheali, Peam; Posada, John A.; Gernaey, Krist

    2015-01-01

    of operating profit for biorefineries producing bioethanol-derived chemicals (247 MM$/a and 241 MM$/a for diethyl ether and 1,3-butadiene, respectively). Second, the optimal designs for upgrading bioethanol (i.e. production of 1,3-butadiene and diethyl ether) performed also better with respect...... to sustainability compared with the petroleum-based processes. In both cases, the effects of the market price uncertainties were also analyzed by performing quantitative economic risk analysis and presented a significant risk of investment for a lignocellulosic biorefinery (12 MM$/a and 92 MM$/a for diethyl ether...

  5. Various Carbon to Carbon Bond Lengths Inter-related via the Golden Ratio, and their Linear Dependence on Bond Energies

    OpenAIRE

    Heyrovska, Raji

    2008-01-01

    This work presents the relations between the carbon to carbon bond lengths in the single, double and triple bonds and in graphite, butadiene and benzene. The Golden ratio, which was shown to divide the Bohr radius into two parts pertaining to the charged particles, the electron and proton, and to divide inter-atomic distances into their cationic and anionic radii, also plays a role in the carbon-carbon bonds and in the ionic/polar character of those in graphite, butadiene and benzene. Further...

  6. Absolute rate constants for the reaction of NO3 radicals with a series of dienes at 295 K

    DEFF Research Database (Denmark)

    Ellermann, T.; Nielsen, O.J.; Skov, H.

    1992-01-01

    The rate constants for the reaction of NO3 radicals with a series of 7 dienes, 1,3-butadiene, isoprene, 2,3-dimethyl-1,3-butadiene, trans-1,3-pentadiene, cis-1,3-pentadiene, trans,trans-2,4-hexadiene, and 1,3-cyclohexadiene, were measured at 295 K and at a total pressure of 1 atm. The rate constant...... were obtained using the absolute technique of pulse radiolysis combined with kinetic UV-VIS spectroscopy. The results are discussed in terms of reactivity trends and previous literature data....

  7. High Performance Graphene Oxide Based Rubber Composites

    OpenAIRE

    Yingyan Mao; Shipeng Wen; Yulong Chen; Fazhong Zhang; Pierre Panine; Tung W. Chan; Liqun Zhang; Yongri Liang; Li Liu

    2013-01-01

    In this paper, graphene oxide/styrene-butadiene rubber (GO/SBR) composites with complete exfoliation of GO sheets were prepared by aqueous-phase mixing of GO colloid with SBR latex and a small loading of butadiene-styrene-vinyl-pyridine rubber (VPR) latex, followed by their co-coagulation. During co-coagulation, VPR not only plays a key role in the prevention of aggregation of GO sheets but also acts as an interface-bridge between GO and SBR. The results demonstrated that the mechanical prope...

  8. Predicting the glass transition temperature as function of crosslink density and polymer interactions in rubber compounds

    Science.gov (United States)

    D'Escamard, Gabriella; De Rosa, Claudio; Auriemma, Finizia

    2016-05-01

    Crosslink sulfur density in rubber compounds and interactions in polymer blends are two of the composition elements that affect the rubber compound properties and glass transition temperature (Tg), which is a marker of polymer properties related to its applications. Natural rubber (NR), butadiene rubber (BR) and styrene-butadiene rubber (SBR) compounds were investigated using calorimetry (DSC) and dynamic mechanical analysis (DMA). The results indicate that the Di Marzio's and Schneider's Models predict with accuracy the dependence of Tg on crosslink density and composition in miscible blends, respectively, and that the two model may represent the base to study the relevant "in service" properties of real rubber compounds.

  9. Hybride Nanocomposites aus Ruß, Nanoclay und NR/BR

    NARCIS (Netherlands)

    Sapkota, Brahmananda; Poikelispää, M.; Das, A.; Dierkes, Wilma K.; Vuorinen, J.

    2013-01-01

    The influence of partial replacement of carbon black (CB) by nanoclay on the curing kinetics of natural rubber/butadiene rubber-based hybrid nanocomposites was studied. The successive replacement of CB by organically modified nanoclays significantly influenced the curing behaviour of the compound:

  10. DFT Studies on cis-1,4-Polymerization of Dienes Catalyzed by a Cationic Rare-Earth Metal Complex Bearing an Ancillary PNP Ligand

    Directory of Open Access Journals (Sweden)

    Xingbao Wang

    2017-02-01

    Full Text Available Dnsity functional theory (DFT calculations have been carried out for the highly selective cis-1,4-polymerization of butadiene catalyzed by a cationic rare-earth metal complex bearing an ancillary PNP ligand. It has been found that the chain initiation and propagation of butadiene polymerization occurs via the favorable cis-1,4-insertion route. The trans-1,4 and 1,2-insertion are unfavorable both kinetically and thermodynamically. The chain growth follows the π-allyl-insertion mechanism. The analyses of energy decomposition of transition states indicate that the likelihood of rival insertion pathways is predominantly controlled by the interaction energy of butadiene with a metal center and the deformation energy of butadiene moiety. The electronic factor of the central metal has a decisive influence on the cis- vs. trans-insertion and the regioselectivity (cis-1,4- vs. cis-1,2-insertion is mainly determined by steric hindrance. Tetrahydrofuran (THF coordination made monomer insertion less favorable compared with THF-free case and had more noticeable impact on the trans-monomer insertion compared with the cis case. During the chain propagation, cis-insertion of monomer facilitates THF de-coordination and the THF molecule could therefore dissociate from the central metal.

  11. Cure and mechanical properties of recycled NdFeB–natural rubber ...

    Indian Academy of Sciences (India)

    Administrator

    composite that can be used as flexible magnets and microwave shields. Several types of elastomers such as natural rubber (NR), butyl rubber (IIR), and acrylonitrile butadiene rubber (NBR) have been tested as polymer matrix for ferrite fillers (Anantharaman et al 2001;. Dishovsky et al 2001; Malini et al 2001, 2003; Moham-.

  12. The effect of heat treatment on the internal structure of nanostructured block copolymer films

    DEFF Research Database (Denmark)

    Sepe, Alessandro; Hoppe, E T; Jaksch, S

    2011-01-01

    We report on the temperature dependence of the nanostructure of thin block copolymer films, as studied using in situ grazing-incidence small-angle x-ray scattering (GISAXS). We focus on spin-coated poly(styrene-b-butadiene) diblock copolymer thin films featuring lamellae perpendicular to the subs...

  13. Magnetron reactively sputtered Ti-DLC coatings on HNBR rubber : The influence of substrate bias

    NARCIS (Netherlands)

    Bui, X.L.; Pei, Y.T.; Hosson, J.Th.M. De

    2008-01-01

    In this study, Ti-containing diamond-like carbon (Ti-DLC) coatings have been deposited on HNBR (hydrogenated nitrile butadiene) rubber and also on Si wafer as reference via unbalanced magnetroli reactive sputtering from a Ti target in C2H2/Ar plasma. The deposition rates of coatings on rubber and Si

  14. Tribological behavior of W-DLC coated rubber seals

    NARCIS (Netherlands)

    Pei, Y.T.; Bui, X.L.; Zhou, X.B.; Hosson, J.Th.M. De

    2008-01-01

    Tungsten-containing diamond-like carbon (W-DLC) coatings have been deposited on FKM (fluorocarbon) and HNBR (hydrogenated nitrile butadiene) rubbers via unbalanced magnetron reactive sputtering from a WC target in a C2H2/Ar plasma. The surface morphology and fracture cross sections of uncoated and

  15. Modification of rubber surface with hydrogenated diamond-like carbon thin films

    NARCIS (Netherlands)

    Pei, Y. T.; Bui, X. L.; De Hosson, J. Th. M.; Laudon, M; Romanowicz, B

    2009-01-01

    Thin films of hydrogenated diamond-like carbon (DLC) have been deposited on hydrogenated nitrile butadiene rubber (HNBR) for reduction of friction and enhancement of wear resistance of dynamic rubber seals, by sputtering graphite targets in C(2)H(2)/Ar plasma. The wax removal and pre-deposition

  16. Modification of rubber surface with DLC thin films for low friction and self lubrication

    NARCIS (Netherlands)

    Bui, X. L.; Pei, Y. T.; Mulder, E. D. G.; De Hosson, J. Th. M.; DeHosson, JTM; Brebbia, CA

    2009-01-01

    Thin films of hydrogenated diamond-like carbon (DLC) have been deposited on hydrogenated nitrile butadiene rubber (HNBR) via magnetron-enhanced plasma chemical vapor deposition (ME-PCVD). Pre-deposition plasma treatment of HNBR substrate is proven to be crucial for the improvement of film

  17. Microstructure and tribological performance of diamond-like carbon films deposited on hydrogenated rubber

    NARCIS (Netherlands)

    Pal, J.P. van der; Martinez Martinez, Diego; Pei, Y.T.; Rudolf, P.; Hosson, J.Th.M. De

    2012-01-01

    In this paper, the microstructure and tribological performance of diamond-like carbon (DLC) films prepared by plasma chemical vapor deposition on hydrogenated nitrile butadiene rubbers (HNBR) are studied. Different negative variations of temperature during film growth were selected by proper changes

  18. Deposition and characterization of hydrogenated diamond-like carbon thin films on rubber seals

    NARCIS (Netherlands)

    Pei, Y.T.; Bui, X.L.; Hosson, J.Th.M. De

    2010-01-01

    Thin films of hydrogenated diamond-like carbon (DLC) have been deposited on hydrogenated nitrile butadiene rubber (HNBR) for reduction of friction and enhancement of wear resistance of dynamic rubber seals. The wax removal and pre-deposition plasma treatment of HNBR substrates are proven to be

  19. Flexible diamond-like carbon films on rubber : On the origin of self-acting segmentation and film flexibility

    NARCIS (Netherlands)

    Pei, Y.T.; Bui, X.L.; Pal, J.P. van der; Martinez-Martinez, D.; Zhou, X.B.; Hosson, J.Th.M. De

    This paper reports an experimental approach to deposit flexible diamond-like carbon (DLC) films on hydrogenated nitrile butadiene rubber (HNBR) with plasma-assisted chemical vapor deposition and an analytical model to describe the self-segmentation mechanism of the DLC films. By making use of the

  20. Microstructure and tribological behavior of tungsten-containing diamondlike carbon coated rubbers

    NARCIS (Netherlands)

    Pei, Y.T.; Bui, X.L.; Zhou, Xiao; Hosson, J.Th.M. De

    2008-01-01

    Tungsten-containing diamondlike carbon (W-DLC) coatings have been deposited on FKM (fluorocarbon), ACM (acrylate), and HNBR (hydrogenated nitrile butadiene) rubbers via unbalanced magnetron reactive sputtering from a WC target in C2H2/Ar plasma. The surface morphology and, fracture cross sections of

  1. Adhesion improvement of hydrogenated diamond-like carbon thin films by pre-deposition plasma treatment of rubber substrate

    NARCIS (Netherlands)

    Bui, X.L.; Pei, Y.T.; Mulder, E.D.G.; Hosson, J.Th.M. De

    2009-01-01

    For reduction of friction and enhancement of wear resistance of dynamic rubber seals, thin films of hydrogenated diamond-like carbon (DLC) have been deposited on hydrogenated nitrile butadiene rubber (HNBR) via magnetron-enhanced plasma chemical vapor deposition (ME-PCVD). Pre-deposition plasma

  2. 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, must...

  3. Three Dimensional (3 D) Printed Sierpinski Patch Antenna

    Science.gov (United States)

    2017-10-25

    the expertise in this field is also rapidly expanding . The 4-year hiring trends in the field of additive manufacturing are shown in Figure 1. The...Testing of Acrylonitrile Butadiene Styrene (ABS), High Impact Polystyrene (HIPS) and Polylactic Acid (PLA) Plastics: A Comparative Study Between

  4. 3D Printing in Makerspaces: Health and Safety Concerns

    Science.gov (United States)

    Bharti, Neelam

    2017-01-01

    3D (three-dimensional) printing is included in makerspaces around the world and has become increasingly affordable and useful. Most makerspaces use Fused Deposition Modeling (FDM)-based 3D printers, using polylactic acid (PLA) and acrylonitrile butadiene styrene (ABS) as printing materials. However, heating PLA and ABS to high temperatures emits…

  5. Structure–property relationships of ‘safe’ aromatic oil based passenger car tire tread rubber compounds

    NARCIS (Netherlands)

    Rathi, Akansha; Hernández, M.; Dierkes, Wilma K.; Bergmann, C.; Noordermeer, Jacobus W.M.; Trimbach, J.; Blume, Anke

    2015-01-01

    In this study, the effect of Treated Distillate Aromatic Extract (TDAE) was investigated in medium styrene/high vinyl solution styrene butadiene rubber (S-SBR) and high cis-polybutadiene rubber (BR). Three properties were evaluated: (i) molecular structure (polarity/aromaticity), (ii) molecular

  6. Structure–property relationships of ‘safe’ aromatic oil based passenger car tire tread rubber compounds

    NARCIS (Netherlands)

    Rathi, Akansha; Hernández, M.; Dierkes, Wilma K.; Bergmann, C.; Trimbach, J.; Blume, Anke

    2016-01-01

    In this study, the effect of TDAE-oil was investigated in functionalized, medium styrene/high vinyl solution styrene butadiene rubber (FsS-SBR) and high cispolybutadiene rubber (BR). Three properties were evaluated: (i) molecular structure (polarity/aromaticity), (ii) molecular weight and (iii)

  7. Accuracy Enhancement of CT Measurements using Data Filtering

    DEFF Research Database (Denmark)

    Stolfi, Alessandro; Kallasse, Maarja-Helena; Carli, Lorenzo

    2016-01-01

    polycarbonate (PC) and acrylonitrile butadiene styrene (ABS), respectively. 3D median filters with different window sizes were taken in account as influence factors, while a variety of dimensional and geometrical tolerances were used as evaluation parameters. All measurands were calibrated using a tactile CMM...

  8. Disease: H00005 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available 04390] ... 1,3-Butadiene [CPD:C16450] Ethylene oxide [CPD:C06548] Rubber industry Beta-2-microglobulin (B2M) [... ... Meta-analysis of mortality and cancer incidence among workers in the synthetic rubber-producing indus...try. ... JOURNAL ... Am J Epidemiol 164:405-20 (2006) DOI:10.1093/aje/kwj252 ... (drug) ...

  9. Disease: H00004 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available ] [KO:K06621] p53 (mutation) [HSA:7157] [KO:K04451] RB1 (mutation) [HSA:5925] [KO:K06618] ... 1,3-Butadiene [CPD:C16450] Rubber industr..., Delzell E. ... TITLE ... An updated study of mortality among North American synthetic rubber industry worker

  10. Synthesis of pyrrolizines by intramolecular capture of 1,4-dipolar intermediates in reactions of enamines with dimethyl acetylenedicarboxylate

    NARCIS (Netherlands)

    Verboom, Willem; Visser, G.W.; Trompenaars, W.P.; Reinhoudt, David; Harkema, Sybolt; van Hummel, G.J.

    1981-01-01

    Solvent polarity and reaction temperature strongly influence the reactions of dimethyl acetylenedicar-boxylate (DMAD) with 1-pyrrolidinyl enamines of acyclic and cyclic ketones. Whereas DMAD and 1-[1-phenyl-2-(phenylthio)ethenyl]pyrrolidine (3) give only a mixture of the isomeric 1,3-butadienes (5)

  11. 3D Printing in Makerspaces: Health and Safety Concerns

    Science.gov (United States)

    Bharti, Neelam

    3D (three-dimensional) printing is included in makerspaces around the world and has become increasingly affordable and useful. Most makerspaces use Fused Deposition Modeling (FDM)-based 3D printers, using polylactic acid (PLA) and acrylonitrile butadiene styrene (ABS) as printing materials. However, heating PLA and ABS to high temperatures emits…

  12. Direct synthesis of inverse hexagonally ordered diblock copolymer/polyoxometalate nanocomposite films

    NARCIS (Netherlands)

    Lunkenbein, T.; Kamperman, M.M.G.; Li, Z.; Bojer, C.; Drechsler, M.; Forster, S.; Wiesner, U.; Muller, A.; Breu, J.

    2012-01-01

    Nanostructured inverse hexagonal polyoxometalate composite films were cast directly from solution using poly(butadiene-block-2-(dimethylamino)ethyl methacrylate) (PB-b-PDMAEMA) diblock copolymers as structure directing agents for phosphomolybdic acid (H(3)[PMo(12)O(40)], H(3)PMo). H(3)PMo units are

  13. Guest driven structural transformation studies of a luminescent metal ...

    Indian Academy of Sciences (India)

    2(DCM).xG] (1 ⊃ G) (OTf = trifluoro methane sulfonate, DCM = Dichloromethane, L (1, 4-bis (4-pyridyl)-2, 3-diaza-1, 3-butadiene) synthesized at room temperature. Free guests DCM were encapsulated in the pores of the MOF. On air drying ...

  14. Controlled Functionalization of Olefin/styrene Copolymers through Free Radical Processes

    NARCIS (Netherlands)

    Passaglia, Elisa; Aglietto, Mauro; Ciardelli, Francesco; Picchioni, Francesco

    2000-01-01

    The functionalization of styrene-b-(ethylene-co-1-butene)-b-styrene triblock copolymer (SEBS) and styrene-co-butadiene (SBR) random copolymer by free radical processes is presented. SEBS was functionalized in the melt with diethyl maleate (DEM) and dicumyl peroxide (DCP) as initiator. The

  15. 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.

  16. Uncertainties in early-stage capital cost estimation of process design – a case study on biorefinery design

    DEFF Research Database (Denmark)

    Cheali, Peam; Gernaey, Krist; Sin, Gürkan

    2015-01-01

    robust decision-making under uncertainties. One of the results using order-of-magnitude estimates shows that the production of diethyl ether and 1,3-butadiene are the most promising with the lowest economic risks (among the alternatives considered) of 0.24 MM$/a and 4.6 MM$/a, respectively....

  17. Economic risk analysis and critical comparison of optimal biorefinery concepts

    DEFF Research Database (Denmark)

    Cheali, Peam; Posada, John A.; Gernaey, Krist

    2016-01-01

    value-added chemicals (diethyl ether and 1,3-butadiene), provides an improved resilience and robustness against market price fluctuations by reducing economic loss by 140 MM$/a (17% IRR); (iii) the economic analysis favors biochemical conversion technologies for a small production/processing capacity...

  18. Role of polyvinyl alcohol in the conductivity behaviour of ...

    Indian Academy of Sciences (India)

    poly(MMA–VC), poly(styrene–AN) and poly(styrene–butadiene) [8–11]. Within this framework, an attempt has been made in the present work to develop a polyethylene glycol-based polymer composite gel electrolyte, namely, polyethylene glycol–polyvinyl alcohol–NH4SCN system. This system has been studied on ac-.

  19. A low-cost lead-acid battery with high specific-energy

    Indian Academy of Sciences (India)

    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 ...

  20. Studies on ethylene-propylene-diene rubber modification by N-chlorothio-N-butyl-benzenesulfonamide

    NARCIS (Netherlands)

    Zhang, Hongmei; Datta, Rabin; Talma, Auke; Noordermeer, Jacobus W.M.

    2009-01-01

    N-Chlorothiosulfonamides have been used to modify ethylene-propylene-diene rubber (EPDM) to enhance the compatibility of EPDM in, e.g., natural rubber (NR)/butadiene rubber (BR)/EPDM blends for ozone resistance. N-Chlorothio-N-butyl-benzenesulfonamide (CTBBS) was selected as a representative for

  1. Development of Low-Friction Elastomers for Stern-Tube Bearings.

    Science.gov (United States)

    1980-07-31

    POLYMER (PHR) Acrylonitrile Butadiene Copolymer ACN 40.0% 100.0 Carbon Black N-774 Particle size 60.0 Carbon Black N-550 Particle size 40.0 Zinc Oxide...pecirie. shall then be rer.-oed from :he bottle and weighed in distilled water (WI ) in immnediate consecutive prucedure to deterni.e the di- ipl .,ce

  2. Studies on blends of cycloaliphatic epoxy resin with varying ...

    Indian Academy of Sciences (India)

    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 ...

  3. Producing alpha-olefins using polyketide synthases

    Energy Technology Data Exchange (ETDEWEB)

    Fortman, Jeffrey L.; Katz, Leonard; Steen, Eric J.; Keasling, Jay D.

    2018-01-02

    The present invention provides for a polyketide synthase (PKS) capable of synthesizing an .alpha.-olefin, such as 1-hexene or butadiene. The present invention also provides for a host cell comprising the PKS and when cultured produces the .alpha.-olefin.

  4. Fractal dimensions of soy protein nanoparticle aggregates determined by dynamic mechanical method

    Science.gov (United States)

    The fractal dimension of the protein aggregates can be estimated by dynamic mechanical methods when the particle aggregates are imbedded in a polymer matrix. Nanocomposites were formed by mixing hydrolyzed soy protein isolate (HSPI) nanoparticle aggregates with styrene-butadiene (SB) latex, followe...

  5. Air sampling and analysis in a rubber vulcanization area.

    Science.gov (United States)

    Rappaport, S M; Fraser, D A

    1977-05-01

    Results of sampling and analysis of air in a rubber vulcanization area are described. Organic compounds were collected on activated charcoal, desorbed with carbon disulfide and analyzed by gas chromatography. Several previously identified substances were quantitated, including styrene, toluene, ethylbenzene, and several oligomers of 1,3-butadiene. Concentrations ranged from 0.007 to 1.1 ppm.

  6. Rheology of high melt strength polypropylene for additive manufacturing

    DEFF Research Database (Denmark)

    Jagenteufel, Ralf; Hofstätter, Thomas; Kamleitner, Florian

    2017-01-01

    Rheological measurements of high melt strength polypropylene (HMS-PP) were used in order to generate master curves describing the shear-dependent viscosity in comparison to acrylonitrile butadiene styrene copolymer (ABS). The latter material showed specific disadvantages in terms of thermal stabi...

  7. Rheological and chemical evaluation on the ageing properties of SBS polymer modified bitumen: From the laboratory to the field

    NARCIS (Netherlands)

    Liu, G.; Nielsen, E.; Komacka, J.; Greet, L.; Ven, M.V.D.

    2014-01-01

    This study investigated the ageing properties of the styrene-butadiene- styrene polymer modified bitumen (SBS PMB) from the laboratory to the field. The virgin SBS PMB had been kept for 23 years and its field-aged binder was extracted from the reclaimed stone matrix asphalt (SMA) after the 22-year

  8. The challenges of silica-silane reinforcement of natural rubber

    NARCIS (Netherlands)

    Dierkes, Wilma K.; Sarkawi, S.S.; Noordermeer, Jacobus W.M.

    2012-01-01

    In recent years, highly-dispersible silica has become the preferred alternative to carbon-black as reinforcing filler for low rolling-resistance tires. However, the application of this filler system is so far limited to passenger car tires, as their treads contain styrene butadiene rubber (SBR). In

  9. Thermal modelling of extrusion based additive manufacturing of composite materials

    DEFF Research Database (Denmark)

    Jensen, Mathias Laustsen; Sonne, Mads Rostgaard; Hattel, Jesper Henri

    -butadiene-styrene (ABS) and thermosetting polyurethane (PU) material extrusion processes. During the experimental evaluation of the produced models it is found that some critical material properties needs to be further investigated to increase the precision of the model. It is however also found that even with only...

  10. Best Practice for the Devulcanization of Sulfur-cured SBR Rubber

    NARCIS (Netherlands)

    Saiwari, Sitisaiyidah; Dierkes, Wilma K.; Noordermeer, Jacobus W.M.; Blume, Anke

    2015-01-01

    In the present paper, special attention will be devoted to thermo-chemical devulcanization of sulfur-cured styrene butadiene rubber (SBR) using diphenyldisulfide (DPDS) as devulcanization aid. SBR is the main component in whole passenger car tire rubber and, at the same time, the most critical one

  11. Pathway for high-quality reclaim by thermal treatment of sulfur-vulcanized SBR

    NARCIS (Netherlands)

    Saiwari, Sitisaiyidah; Dierkes, Wilma K.; Noordermeer, Jacobus W.M.

    2011-01-01

    De-vulcanization of SBR (Styrene Butadiene Rubber) is a challenge, as the broken polymer chains tend to re-arrange. This influences the properties of the reclaimed and re-vulcanized rubber, and reduces the quality of the recycled material. Within this study, the breakdown of sulfur-cured SBR in a

  12. A comparison of flexural strengths of polymer (SBR and PVA) modified, roller compacted concrete.

    Science.gov (United States)

    Karadelis, John N; Lin, Yougui

    2015-09-01

    This brief article aims to reveal the flexural performance, including the equivalent flexural strength of PVA (Polyvinyl Alcohol) modified concrete by comparing it primarily with that of SBR (Styrene Butadiene Rubber) concrete. This data article is directly related to Karadelis and Lin [6].

  13. Chemical Contaminant and Decontaminant Test Methodology Source Document. Second Edition

    Science.gov (United States)

    2012-07-01

    rubber – styrene butadiene rubber ( SBR ); 60A hardness; black color, fabric-reinforced SBR rubber , 1/8 in. thick. Navy Ship Topcoat- Painted Carbon... APPLICATIONS INTERNATIONAL CORPORATION Gunpowder, MD 21010-0068 July 2012 Approved for public release; distribution is unlimited... APPLICATIONS INTERNATIONAL CORPORATION Gunpowder, MD 21010-0068 REPORT DOCUMENTATION PAGE Form Approved OMB No. 0704-0188 Public reporting

  14. A comparison of flexural strengths of polymer (SBR and PVA modified, roller compacted concrete

    Directory of Open Access Journals (Sweden)

    John N. Karadelis

    2015-09-01

    Full Text Available This brief article aims to reveal the flexural performance, including the equivalent flexural strength of PVA (Polyvinyl Alcohol modified concrete by comparing it primarily with that of SBR (Styrene Butadiene Rubber concrete. This data article is directly related to Karadelis and Lin [6].

  15. Improved natural rubber composites reinforced with a complex filler network of biobased nanoparticles and ionomer

    Science.gov (United States)

    Biobased rubber composites are renewable and sustainable. Significant improvement in modulus of rubber composite reinforced with hydrophilic filler was achieved with the inclusion of ionomers. Soy particles aided with ionomer, carboxylated styrene-butadiene (CSB), formed a strong complex filler netw...

  16. 21 CFR 177.1200 - Cellophane.

    Science.gov (United States)

    2010-04-01

    ...-butadiene-styrene copolymer resins Do. Acrylonitrile-styrene copolymer resins Do. Acrylonitrile-vinyl...-vinyl acetate copolymers complying with § 177.1350 2-Ethylhexyl alcohol 0.1 percent for use only as... cellophane base sheet. Polypropylene complying with § 177.1520 Polystyrene As the basic polymer. Polyvinyl...

  17. 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

  18. Simple 3D Printed Scaffold-Removal Method for the Fabrication of Intricate Microfluidic 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

  19. Effect of coagulant dosage on molecular weight of the rubber fractions allocated and vulcanizates physical-mechanical properties

    Directory of Open Access Journals (Sweden)

    I. N. Pugacheva

    2013-01-01

    Full Text Available The influence of dosage and nature of coagulation agents on molecular weight secreted butadiene-styrene rubber is considered. It is established that the increase of coagulant expense is accompanied by increase of molecular weight that is reflected in indicators received vulcanizates.

  20. Pramana – Journal of Physics | Indian Academy of Sciences

    Indian Academy of Sciences (India)

    2015-11-27

    Nov 27, 2015 ... Home; Journals; Pramana – Journal of Physics. B G Soares. Articles written in Pramana – Journal of Physics. Volume 69 Issue 3 September 2007 pp 435-443 Research Articles. Variation of long periodicity in blends of styrene butadiene, styrene copolymer/polyaniline using small angle X-ray scattering data.

  1. STRUCTURAL TRANSFORMATIONS IN FILLED WITH ACTIVE TECHNICAL CARBON SKB AT DEFORMATION THROUGH A CAPILLARY

    Directory of Open Access Journals (Sweden)

    V. I. Korchagin

    2012-01-01

    Full Text Available Use capillary viscometry has allowed to receive empirical dependences of change of the maintenance carbon-kauchuvogo of gel from speed of shift, degree of filling, temperatures and durations of influence in filled with technical carbon of mark К-354 butadien-stirolnom rubber SKS-30ARK.

  2. N,N-Diethyl-1-Tosyl-3-Indoleglyoxylamide as a Dienophile in Diels-Alder Reactions. Hyperbaric vs. Thermal Conditions

    Directory of Open Access Journals (Sweden)

    B. Biolatto

    2000-03-01

    Full Text Available Under high pressure conditions, the Diels-Alder reaction involving N,N-diethyl-1-tosyl-3-indoleglyoxylamide and 1-(N-acetyl-N-propylamino-1,3-butadiene produces a highly functionalized intermediate for the synthesis of Indole Alkaloids, in shorter times and higher yields than under thermal conditions.

  3. Effect of Phthalic Anhydride Modified Soy Protein on Viscoelastic Properties of Polymer Composites

    Science.gov (United States)

    Phthalic anhydride (PA) modified soy protein isolates (SPI), both hydrolyzed and un-hydrolyzed, are investigated as reinforcement fillers in styrene-butadiene (SB) composites. The modification of SPI by PA increases the number of carboxylic acid functional groups on the protein surface and therefor...

  4. Effects of the Hydrophobicity of the Reactants on Diels-Alder Reactions in Water

    NARCIS (Netherlands)

    Meijer, Ale; Otto, Sijbren; Engberts, Jan B.F.N.

    1998-01-01

    To assess the importance of the hydrophobicity of different parts of diene and dienophile on the aqueous acceleration of Diels-Alder reactions, second-order rate constants have been determined for the reactions of cyclopentadiene (1), 2,3-dimethyl-1,3-butadiene (4), and 1,3-cyclohexadiene (6) with

  5. Polybutadiene (Jumping Rubber)

    Science.gov (United States)

    Fine, Leonard W.

    1996-01-01

    This laboratory procedure starts with a violet suspension of an 'alfin' catalyst being added to a bottle containing a solution of 1,3-butadiene in pentane. The bottle is corked and shaken for several seconds. The mixture sets to a gel, and within 2 minutes the contents erupt from the bottle.

  6. A comparison of reflectance properties on polymer micro-structured functional surface

    DEFF Research Database (Denmark)

    Regi, Francesco; Li, Dongya; Nielsen, Jannik Boll

    by their pitch distance and their angle in respect to the surface (Figure 2). The geometry was obtained by precision milling of a tool steel bar and replicated through silicone replica technology [2], and by hot embossing using Acrylonitrile Butadiene Styrene (ABS). A digital microscope has been used...

  7. 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...

  8. Simultaneous determination of the styrene unit content and assessment of molecular weight of triblock copolymers in adhesives by a size exclusion chromatography method.

    Science.gov (United States)

    Wang, Mingfang; Wang, Yuerong; Luo, Pei; Zhang, Hongyang; Zhang, Min; Hu, Ping

    2017-10-01

    The content of styrene units in nonhydrogenated and hydrogenated styrene-butadiene-styrene and styrene-isoprene-styrene triblock copolymers significantly influences product performance. A size exclusion chromatography method was developed to determine the average styrene content of triblock copolymers blended with tackifier in adhesives. A complete separation of the triblock copolymer from the other additives was realized with size exclusion chromatography. The peak area ratio of the UV and refraction index signals of the copolymers at the same effective elution volume was correlated to the average styrene unit content using nuclear magnetic resonance spectroscopy with commercial copolymers as standards. The obtained calibration curves showed good linearity for both the hydrogenated and nonhydrogenated styrene-butadiene-styrene and styrene-isoprene-styrene triblock copolymers (r = 0.974 for styrene contents of 19.3-46.3% for nonhydrogenated ones and r = 0.970 for the styrene contents of 23-58.2% for hydrogenated ones). For copolymer blends, the developed method provided more accurate average styrene unit contents than nuclear magnetic resonance spectroscopy provided. These results were validated using two known copolymer blends consisting of either styrene-isoprene-styrene or hydrogenated styrene-butadiene-styrene and a hydrocarbon tackifying resin as well as an unknown adhesive with styrene-butadiene-styrene and an aromatic tackifying resin. The methodology can be readily applied to styrene-containing polymers in blends such as poly(acrylonitrile-butadiene styrene). © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  9. 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.

  10. Phase Control of BR/SBR Blends by Silica Particles

    Science.gov (United States)

    Inai, Motoyuki; Aizawa, Seiji; Ito, Masayoshi

    A phase control of butadiene rubber (BR)/styrene-butadiene rubber (SBR) blends was examined by using silica particles. The phase structure of the blends was qualitatively evaluated from transmission electron microscope (TEM) observation and temperature dependence of mechanical tanδ. It was found that the temperature dependence of tanδ was dependent on the size of agglomerate formed by silica particles in the blend. The vulcanized blends with small agglomerates showed a single tanδ peak suggesting a pseudo-miscible state. The vulcanized blends with large agglomerates showed two tanδ peaks corresponding to the Tgs of BR and SBR. The mutual dissolution of BR and SBR phases above the UCST line where the vulcanization was carried out might be disturbed by large agglomerates formed by silica particles in the blends.

  11. Influence of Adhesive System on Performance of SiO/C Lithium-ion Battery

    Directory of Open Access Journals (Sweden)

    Teng Xin

    2015-01-01

    Full Text Available Silicon based anode material is turning into the research hot point of lithium-ion battery material field due to Si inside supporting higher capacity. Furthermore binder applied as major accessory material of anode system could bring anode material & current collector together, thus the influence given by binder system to battery performance becomes the key point. The paper describes the procedure of adopting commercial LiCoO2 SiO/C as composite material & electrolyte, with using styrene butadiene rubber and acrylic acid copolymer as binder to figure out lithium-ion battery with 2.5Ah, which is testified to present better performance on cold temperature & cycle life plus having a little bit swelling compared with the lithium-ion battery using only styrene butadiene rubber as binder.

  12. Properties of Elastomeric Composites with Functionalized Carbon Nanomaterial

    Science.gov (United States)

    Shashok, Zh. S.; Prokopchuk, N. R.; Vishnevskii, K. V.; Krauklis, A. V.; Borisevich, K. O.; Borisevich, I. O.; Zhdanok, S. A.

    2017-03-01

    The influence of two different nanomaterials on the properties of elastomeric composites based on general- and special-purpose rubbers has been investigated. For the elastomeric matrix, we used a combination of synthetic polyisopropene (SKI-3) and stereoregular butadiene (SKD) caoutchoucs in one case and butadiene-nitrile caoutchouc containing 27-30% of bound acrylic acid nitrile (BNKS-28) in the other case. For additives, nanomaterials of two types were used. To determine the degree of interaction of the additives with the elastomeric matrix, complex tests of rubber mixes and vulcanizates based on them were carried out, in which the following indices were determined: the Mooney viscosity, the relaxation and vulcanization characteristics of the mixes, the elastic-strength properties of the vulcanizates before and after thermal ageing, their resistance to thermal ageing, and the mechanical loss tangent.

  13. Pengaruh suhu vulkanisasi terhadap sifat mekanis vulkanisat karet alam dan karet akrilonitril-butadiena

    Directory of Open Access Journals (Sweden)

    Norma Arisanti Kinasih

    2015-12-01

    Full Text Available Natural and acrylonitrile-butadiene rubbers possess different vulcanization characteristics. Selection of the vulcanization system and temperature affects the mechanical properties of vulcanized natural rubber (NR and acrylonitrile-butadiene rubber (NBR. In the present work, the effect of vulcanization temperature (150, 160, 170 and 180oC on the mechanical properties of NR and NBR vulcanizates was studied. The effect of different vulcanization system (semi efficient, efficient and sulfur donor was studied in NR blends, while the effect of different acrylonitrile content (26, 28 and 33 wt % was studied in NBR blends. The NBR curing characteristics and mechanical properties data showed that vulcanization at low temperature (150oC was suitable for low acrylonitrile-NBR, whereas that at high temperature (170oC was suitable for high acrylonitrile-NBR. In addition, the semi efficient system at low temperature vulcanization (150oC was suitable for natural rubber.

  14. Covalent Fluorination Strategies for the Surface Modification of Polydienes.

    Science.gov (United States)

    De Bruycker, Kevin; Delahaye, Maarten; Cools, Pieter; Winne, Johan; Prez, Filip E Du

    2017-06-01

    Nonreactive additives are widely applied to enhance polymer properties but can leach out of the material over time. In this work, two essentially different fluorinated additives bearing a triazolinedione moiety are synthesized and grafted on several polydiene backbones (acrylonitrile-butadiene-styrene, styrene-butadiene, and styrene-isoprene-styrene (SIS) copolymers), either by dip-coating or by reaction in solution. The resulting polymers are analyzed by contact angle goniometry, size exclusion chromatography, and NMR, infrared, and X-ray photoelectron spectroscopy. Independent of the modification procedure, the fluorophilic perfluoroalkyl additive is found at the material surface, thereby yielding a more hydrophobic surface. For SIS thermoplastic elastomers, for example, contact angles up to 125° can be obtained. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  15. The mechanism of vinylacetylene (VA) hydrochlorination

    Energy Technology Data Exchange (ETDEWEB)

    Shestakov, G.K.; Belskii, F.I.; Airyan, S.M.; Temkin, O.N.

    1978-03-01

    The mechanism of vinylacetylene (VA) hydrochlorination in a cupric chloride solution was studied at 50/sup 0/C in a gradientless flow reactor, and chromatographic analysis identified 2- and 1-chloro-1,3-butadienes as the main products. Analysis of the reaction kinetics showed that CuCl catalyzed both 1,4 and 1,2 (Markovnikov and anti-Markovnikov types) addition of HCl to VA and that no VA conversion occurred without CuCl. The formation of both products occurred via similar many-route mechanisms, with at least one of the routes involving formation and isomerization of 4-chloro-1,2-butadiene (''allene''). Based on the results of this study together with published data on hydrochlorination and hydration of acetylene and methylacetylene, some conclusions on the effect of substituents on the mechanism of hydrochlorination of acetylene compounds were reached. Tables, graphs, and 15 references.

  16. Single-atom gold catalysis in the context of developments in parahydrogen-induced polarization.

    Science.gov (United States)

    Corma, Avelino; Salnikov, Oleg G; Barskiy, Danila A; Kovtunov, Kirill V; Koptyug, Igor V

    2015-05-04

    A highly isolated monoatomic gold catalyst, with single gold atoms dispersed on multiwalled carbon nanotubes (MWCNTs), has been synthesized, characterized, and tested in heterogeneous hydrogenation of 1,3-butadiene and 1-butyne with parahydrogen to maximize the polarization level and the contribution of the pairwise hydrogen addition route. The Au/MWCNTs catalyst was found to be active and efficient in pairwise hydrogen addition and the estimated contributions from the pairwise hydrogen addition route are at least an order of magnitude higher than those for supported metal nanoparticle catalysts. Therefore, the use of the highly isolated monoatomic catalysts is very promising for production of hyperpolarized fluids that can be used for the significant enhancement of NMR signals. A mechanism of 1,3-butadiene hydrogenation with parahydrogen over the highly isolated monoatomic Au/MWCNTs catalyst is also proposed. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  17. FTIR analysis on aging characteristics of ABS/PC blend under UV-irradiation in air

    Science.gov (United States)

    Li, Jiarong; Chen, Fu; Yang, Long; Jiang, Long; Dan, Yi

    2017-09-01

    Fourier Transform Infrared Spectroscopy (FTIR) is adopted to study the aging characteristics of poly(acrylonitrile-butadiene-styrene)/polycarbonate (ABS/PC) blend under UV-irradiation in air by analyzing the variation of the three main absorbance at about 967 cm- 1, 1720 cm- 1 and 3420 cm- 1 associated with carbon-hydrogen bonds belonging to 1,4 butadiene, carbonyl and hydroxyl groups, respectively. Results indicate that, under UV-irradiation in air, the photo-oxidation of the blend is not a simple combination of the photo-oxidation of corresponding ABS and PC themselves and takes place predominantly at the ABS component. Due to the interaction between the two components and the Fries rearrangement taken place in the PC component during the UV-irradiation in air, the ABS/PC blends behave higher photo-stability than ABS has.

  18. Physical and Mechanical Characteristics of Kevlar Fiber-Reinforced PC/ABS Composites

    OpenAIRE

    Kuljira Sujirote; Parkpoom Lorjai; Sarawut Rimdusit; Sunan Tiptipakorn

    2012-01-01

    In this research, the composites between polycarbonate (PC) and acrylonitrile-butadiene-styrene (ABS) alloy and Kevlar fiber were prepared. The flexural and tensile properties of PC/ABS alloy and its composites were determined using a universal testing machine. The synergistic behavior of flexural modulus was observed for all regions of PC contents, while the synergism of flexural strength and tensile strength were found in some PC contents. It was found that the optimum weight ratio of PC:AB...

  19. Estudi de la funcionalitat dels monòmers en la síntesi de polímers per l'acabat de la pell

    OpenAIRE

    Gutiérrez Muntada, Jordi

    2017-01-01

    In the leather industry, the finish process uses many types of resins including butadiene, acrylic and polyurethanes, aided by auxiliaries as pigments, waxes etc. that give touch to different articles that are currently marketed. This project tries to characterize a very particular time and extensive resins, acrylic resins. This is from a base polymer incorporating different functional groups; these groups will shape the functional acrylic resin and consequently will configure particular...

  20. 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...

  1. Frictional behaviour of some sealing elastomers in lubricated sliding

    OpenAIRE

    M Mofidi; Prakash, Braham

    2012-01-01

    Frictional behaviour of four sealing elastomers, including an acrylonitrile butadienerubber (NBR), a hydrogenated acrylonitrile butadiene rubber (HNBR), an acrylate rubber(ACM) and a fluoroelastomer (FKM), sliding against a steel surface under unidirectionallubricated conditions have been studied. The lubricant used in this study was paraffinic oilwith no additive and the experiments were conducted under a block-on-ring testconfiguration. The friction coefficients of the elastomers have been ...

  2. A novel method for recovery of acidic sludge of used-motor oil reprocessing industries to bitumen using bentonite and SBS

    OpenAIRE

    Ahmad Jonidi Jafari; malek hassanpour; Mitra Gholam; Mehdi Farzadkia

    2014-01-01

    ABSTRACT Acidic sludge is a by-product from used motor oil reprocessing industries, which thousand tons of this sludge are disposed into the environment as a hazardous waste material daily. The acidic sludge contains unsaturated compounds that are polar and asphaltene. The bitumen under certain conditions is produced from mixing of bentonite, polymer styrene – butadiene – styrene (SBS), and acidic sludge. Context and purpose: The objective of this study was the recovery of acidic sludge...

  3. Polymer modification of bitumen : Advances and challenges

    OpenAIRE

    Zhu, Jiqing; Birgisson, Björn; Kringos, Niki

    2014-01-01

    Advances and challenges in the field of bitumen polymer modification for road construction during the last 40 years are reviewed in this paper. The history of bitumen polymer modification is described chronologically. Some popular plastomers and thermoplastic elastomers in bitumen modification are discussed regarding their advantages and disadvantages, including polyethylene (PE), polypropylene (PP), ethylene-vinyl acetate (EVA), ethylene-butyl acrylate (EBA), styrene-butadiene-styrene (SBS),...

  4. Elastomers for Tracked Vehicles: 1980-1997 Program to Improve Durability of Rubber Tank Pads for Army Tracked Vehicles

    Science.gov (United States)

    2015-06-01

    into more stable single bonds. Because of the reduction in double bonds, HNBR provides superior resistance to ozone , weathering, and heat when compared...PBD-2. Synpol E-BR 8418 (containing 20 parts of high aromatic oil ) and Nipol BR-1245 BRs were used in formulations PBD-5 and PBD-8, respectively...methods for rubber-evaluation of SBR (styrene-butadiene rubber) including mixtures with oil . West Conshohocken (PA): ASTM International; 2010. ASTM D

  5. Relaxation of Spin Polarized $^3$He in Mixtures of $^3$He and $^4$He at $\\sim$330 mK

    CERN Document Server

    Ye, Q; Zheng, W; Dutta, D; Dubose, F; Golub, R; Huffman, P; Swank, C; Korobkina, E; 10.1103/PhysRevA.80.023403

    2009-01-01

    We report the measurements of depolarization probabilities of polarized $^3$He in a rectangular acrylic cell with a deuterated tetraphenyl butadiene-doped deuterated polystyrene coating filled with superfluid $^4$He at $\\sim$330 mk with a magnetic holding field of $\\sim$7.3 G. We achieve a wall depolarization probability of $\\sim1.0\\times10^{-7}$. Such a surface will find application in a new experiment searching for the neutron electric dipole moment and other applications.

  6. Impacts of compact growth and electric vehicles on future air quality and urban exposures may be mixed.

    Science.gov (United States)

    Yu, Haofei; Stuart, Amy L

    2017-01-15

    'Smart' growth and electric vehicles are potential solutions to the negative impacts of worldwide urbanization on air pollution and health. However, the effects of planning strategies on distinct types of pollutants, and on human exposures, remain understudied. The goal of this work was to investigate the potential impacts of alternative urban designs for the area around Tampa, Florida USA, on emissions, ambient concentrations, and exposures to oxides of nitrogen (NOx), 1,3-butadiene, and benzene. We studied three potential future scenarios: sprawling growth, compact growth, and 100% vehicle fleet electrification with compact growth. We projected emissions in the seven-county region to 2050 based on One Bay regional visioning plan data. We estimated pollutant concentrations in the county that contains Tampa using the CALPUFF dispersion model. We applied residential population projections to forecast acute (highest hour) and chronic (annual average) exposure. The compact scenario was projected to result in lower regional emissions of all pollutants than sprawl, with differences of -18%, -3%, and -14% for NOx, butadiene, and benzene, respectively. Within Hillsborough County, the compact form also had lower emissions, concentrations, and exposures than sprawl for NOx (-16%/-5% for acute/chronic exposures, respectively), but higher exposures for butadiene (+41%/+30%) and benzene (+21%/+9%). The addition of complete vehicle fleet electrification to the compact scenario mitigated these in-county increases for the latter pollutants, lowering predicted exposures to butadiene (-25%/-39%) and benzene (-5%/-19%), but also resulted in higher exposures to NOx (+81%/+30%) due to increased demand on power plants. These results suggest that compact forms may have mixed impacts on exposures and health. 'Smart' urban designs should consider multiple pollutants and the diverse mix of pollutant sources. Cleaner power generation will also likely be needed to support aggressive adoption

  7. Thermomechanical behavior of SBR reinforced with nanotubes functionalized with polyvinylpyridine

    Science.gov (United States)

    De Falco, A.; Lamanna, M.; Goyanes, S.; D'Accorso, N. B.; Fascio, M. L.

    2012-08-01

    The mechanical and thermal behavior of composites consisting on a styrene-butadiene rubber (SBR) matrix with a sulphur/accelerator system and multiwalled carbon nanotubes functionalized with poly-4-vinylpyridine (MWCNT-PVP) as reinforcement, were studied. The materials were tested with stress-strain tensile tests, DMTA and DSC for thermal properties. A strong increase in the plastic behavior with slight decrease of its elastic Modulus and Tg led to unexpected results.

  8. Synthesis and Characterization of Polypyrrole Coated SBR Composites

    Science.gov (United States)

    Mathew, Anisha Mary; Neena, P.; Prasanth, S.; Panwar, N. S.; Pradeep, P.

    2008-04-01

    Conducting polymer of styrene butadiene rubber has been synthesized by chemical doping method. Subsequently the samples were coated with an intrinsically conducting polymer shell (ICP) of polypyrrole. The polymer shell was synthesized by chemical route method after the preparation of conducting polymer powder of SBR. The chemical structure of the composite was analyzed by taking the FTIR spectra. Electrical conductivity of the new hybrid material is found to be same as the conductivity of polypyrrole.

  9. Group 4 Metal Polyhydrides : Synthesis, Structure, and Reactivity of Tetrakis[(pentamethylcyclopentadienyl)hafnium dihydride chloride

    NARCIS (Netherlands)

    Booij, Martin; Blenkers, Joop; Sinnema, Jacobus C.M.; Meetsma, Auke; Bolhuis, Fré van; Teuben, Jan H.

    The polyhydride [Cp*HfH2Cl]4 was prepared by high-pressure hydrogenation of Cp*Hf(C6H10)Cl (C6H10 = 2,3-dimethyl-1,3-butadiene) or Cp*Hf(COT)Cl (COT = cyclooctatetraene). The structure of [Cp*HfH2Cl]4 was determined by X-ray diffraction. The compound crystallizes in the tetragonal space group P421m

  10. Inhalation Toxicology Research Institute Annual Report, 1992-1993

    Science.gov (United States)

    1993-11-01

    butadiene are the mono- and diepoxide; both have been shown to be mutagenic and are the putative ultimate carcinogens. Mice are much more efficient at...by either cytochrome P-450 or by myeloperoxidase. Our results support earlier findings (Tice, R. R. et al. Environ. Mutagen . 9: 235, 1987) that one...particulate matter ( TPM )/m3, except during the first week when the rats were exposed to 50% of the target concentrations. Table 1 Experimental Design

  11. Design, synthesis, characterization and study of novel conjugated polymers

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Wu [Iowa State Univ., Ames, IA (United States)

    1997-06-24

    After introducing the subject of conjugated polymers, the thesis has three sections each containing a literature survey, results and discussion, conclusions, and experimental methods on the following: synthesis, characterization of electroluminescent polymers containing conjugated aryl, olefinic, thiophene and acetylenic units and their studies for use in light-emitting diodes; synthesis, characterization and study of conjugated polymers containing silole unit in the main chain; and synthesis, characterization and study of silicon-bridged and butadiene-linked polythiophenes.

  12. Thermomechanical behavior of SBR reinforced with nanotubes functionalized with polyvinylpyridine

    Energy Technology Data Exchange (ETDEWEB)

    De Falco, A. [Universidad de Buenos Aires, FCEyN, Depto. de Fisica, LPyMC, Pabellon I, Buenos Aires 1428 (Argentina); Lamanna, M. [Universidad de Buenos Aires, FCEyN, Depto. de Quimica Organica, Centro de Investigaciones en Hidratos de Carbono (CIHIDECAR) (Argentina); Goyanes, S. [Universidad de Buenos Aires, FCEyN, Depto. de Fisica, LPyMC, Pabellon I, Buenos Aires 1428 (Argentina); Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) (Argentina); D' Accorso, N.B. [Universidad de Buenos Aires, FCEyN, Depto. de Quimica Organica, Centro de Investigaciones en Hidratos de Carbono (CIHIDECAR) (Argentina); Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) (Argentina); Fascio, M.L., E-mail: mfascio@qo.fcen.uba.ar [Universidad de Buenos Aires, FCEyN, Depto. de Quimica Organica, Centro de Investigaciones en Hidratos de Carbono (CIHIDECAR) (Argentina)

    2012-08-15

    The mechanical and thermal behavior of composites consisting on a styrene-butadiene rubber (SBR) matrix with a sulphur/accelerator system and multiwalled carbon nanotubes functionalized with poly-4-vinylpyridine (MWCNT-PVP) as reinforcement, were studied. The materials were tested with stress-strain tensile tests, DMTA and DSC for thermal properties. A strong increase in the plastic behavior with slight decrease of its elastic Modulus and Tg led to unexpected results.

  13. Removal of organobromine compounds from the pyrolysis oils of flame retarded plastics using zeolite catalysts\\ud

    OpenAIRE

    Hall, W.J.; Williams, P.T.

    2008-01-01

    Two flame retarded plastics have been pyrolysed in the presence of two Zeolite catalysts to remove the organobromine compounds from the derived pyrolysis oil. The flame retarded plastics were, acrylonitrile – butadiene – styrene (ABS) that was flame retarded with tetrabromobisphenol A and high-impact-polystyrene (HIPS) that was flame retarded with decabromodiphenyl ether. The two catalysts investigated were Zeolite ZSM-5 and Y-Zeolite. Pyrolysis was carried out in a fixed bed reactor at a fin...

  14. Stored energy function of rubberlike materials derived from simple tensile data.

    Science.gov (United States)

    Peng, T. J.; Landel, R. F.

    1972-01-01

    An explicit formulation is developed to obtain the stored energy function, based on the Valanis-Landel separable symmetric stored energy function. This formulation is applicable to any multiaxial stress state, from simple tensile data alone, for those cases in which the stored energy function is a separable function of the stretch ratios. By direct comparison, it is also shown that styrene butadiene rubber, at least over a specific range, follows this postulated separable form.

  15. 3D-Printed Millimeter Wave Structures

    Science.gov (United States)

    2016-03-14

    demonstrates the resolution of the printer with a 10 micron nozzle. Figure 2: Measured loss tangent of SEBS and SBS samples. 3D - Printed Millimeter... 3D printing of styrene-butadiene-styrene (SBS) and styrene ethylene/butylene-styrene (SEBS) is used to demonstrate the feasibility of 3D - printed ...Additionally, a dielectric lens is printed which improves the antenna gain of an open-ended WR-28 waveguide from 7 to 8.5 dBi. Keywords: 3D printing

  16. Scramjet Combustor Simulations Using Reduced Chemical Kinetics for Practical Fuels

    Science.gov (United States)

    2003-12-01

    mol% n-dodecane, 5.5 mol% iso-octane, 10 mol% methylcyclohexane, 11 mol% toluene , and 1 mol% benzene. The mechanism reproduces the profiles of fuel...C12H25, butadiene, butene, isobutane, C5H10, methyl-cylcohexane, H2O, CO, CO2, O2, OH, H2O2, C7H14, CH2O, CH2CO, benzaldehyde , iso-octane, dodecane

  17. The relative fire resistance of select thermoplastic materials. [for aircraft interiors

    Science.gov (United States)

    Kourtides, D. A.; Parker, J. A.

    1978-01-01

    The relative thermal stability, flammability, and related thermochemical properties of some thermoplastic materials currently used in aircraft interiors as well as of some candidate thermoplastics were investigated. Currently used materials that were evaluated include acrylonitrile butadiene styrene, bisphenol A polycarbonate, polyphenylene oxide, and polyvinyl fluoride. Candidate thermoplastic materials evaluated include: 9,9-bis(4-hydroxyphenyl)fluorene polycarbonate-poly(dimethylsiloxane) block polymer, chlorinated polyvinylchloride homopolymer, phenolphthalein polycarbonate, polyethersulfone, polyphenylene sulfide, polyarylsulfone, and polyvinylidene fluoride.

  18. Lithium metal doped electrodes for lithium-ion rechargeable chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Gao; Battaglia, Vince; Wang, Lei

    2016-09-13

    An embodiment of the invention combines the superior performance of a polyvinylidene difluoride (PVDF) or polyethyleneoxide (POE) binder, the strong binding force of a styrene-butadiene (SBR) binder, and a source of lithium ions in the form of solid lithium metal powder (SLMP) to form an electrode system that has improved performance as compared to PVDF/SBR binder based electrodes. This invention will provide a new way to achieve improved results at a much reduced cost.

  19. Thermal Analysis Characterization of Elastomers and Carbon Black Filled Rubber Composites for Army Applications

    Science.gov (United States)

    1985-06-01

    RUBBER COMPOSITES FOR ARMY APPLICATIONS 6. PERFORMING ORO. REPORT NUMBER 7. AUTHOR(q) S. CONTRACT OR GRANT NUMBER(41) Robert E. Sacher, Domenic P...Roadwheei Side SP - Standard Products SBR - Styrene-butadiene Rubber SR - Synthetic Rubber ( SBR or SBR -BR) TR - Track Rubber U - Uncured iii... applications ranging from automotive and aircraft tires to rubber belts, hoses, and seals. Although thermal studies on rubber materials closely

  20. Environmentally Friendly Adhesives and Sealants for Army Applications

    Science.gov (United States)

    2008-12-01

    styrene-butadiene rubber ( SBR ), and nitrile. One brush coat of the adhesive material was applied to the prepared surfaces of the rubber strips...Unclassified Title Environmentally Friendly Adhesives and Sealants for Army Applications 3. Author(s) Faye R. Toulan, Felicia Levine, Leslie...TYPE N/A 3. DATES COVERED - 4. TITLE AND SUBTITLE Environmentally Friendly Adhesives And Sealants For Army Applications 5a. CONTRACT NUMBER

  1. Improved Mechanical Integrity of ALD-Coated Composite Electrodes for Li-Ion Batteries

    Science.gov (United States)

    2011-01-01

    car- boxymethyl cellulose CMC and styrene butadiene rubber SBR binders,5 and heat-treatment,6 as well as carbon-based matrices.7 However, many of...potential of these coatings for high-energy density Li-ion batteries suitable for vehicular applications . © 2010 The Electrochemical Society. DOI: 10.1149...these methods may be quite difficult to scale for Li-ion battery production for vehicular applications . In our previous work, we showed considerable

  2. Waterborne Polymeric Films.

    Science.gov (United States)

    1979-12-01

    in the preparation of synthetic rubber for tires. Even in the modern world the term SBR rubber is a common phrase. Since the styrene-butadiene...homopolymers (TgI . . Tan).12 For applications requiring toughness and moisture barrier properties, it is frequently desirable to incorporate styrene (12a...acrylic or styrenated acrylics. Other applications may require features attributed to other vinyl containing compounds such as halides (12b), ethers

  3. Demonstration/Validation of Hazardous Air Pollutant-Free Adhesive Replacement for Federal Specification MMM-A-1617 Used on the M109A6 Paladin Heavy Brigade Combat Vehicle

    Science.gov (United States)

    2013-09-01

    perimeter of the hatch door. ......................................6 Figure 5. Adhesive application on rubber seal (left) and aluminum channel...natural rubber base, synthetic natural (polyisoprene), styrene butadiene ( SBR ), reclaim, or combination. • Type II: Oil-resistant polychloroprene rubber ...FA-1051) for specification MMM-A-1617 with the HAP- free alternative (3M-847). The specific application was to replace the rubber gasket of the

  4. Study of Polymer Material Aging by Laser Mass Spectrometry, UV-Visible Spectroscopy, and Environmental Scanning Electron Microscopy

    OpenAIRE

    Junien Exposito; Claude Becker; David Ruch; Frédéric Aubriet

    2007-01-01

    Dyed natural rubber (NR) and styrene butadiene rubber (SBR), designed for outdoor applications, were exposed to an accelerated artificial aging in xenon light. The aging results in the deterioration of the exposed surface material properties. The ability of dyed polymers to withstand prolonged sunlight exposure without fading or undergoing any physical deterioration is largely determined not only by the photochemical characteristics of the absorbing dyestuff itself but also by the polymer str...

  5. 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.

  6. Improved TPB-coated light guides for liquid argon TPC light detection systems

    OpenAIRE

    Moss, Z.; Bugel, L.; Collin, G.; Conrad, J. M.; Jones, B.J.P.; Moon, J.; Toups, M; Wongjirad, T1

    2015-01-01

    Scintillation light produced in liquid argon (LAr) must be shifted from 128 nm to visible wavelengths in light detection systems used for liquid argon time-projection chambers (LArTPCs). To date, LArTPC light collection systems have employed tetraphenyl butadiene (TPB) coatings on photomultiplier tubes (PMTs) or plates placed in front of the PMTs. Recently, a new approach using TPB-coated light guides was proposed. In this paper, we report on light guides with improved attenuation lengths abo...

  7. Polysiloxane-Based Organoclay Nanocomposites as Flame Retardants

    Science.gov (United States)

    2013-01-01

    appeared to typically gener- ate more thermally stable composites. These results are comparable to organoclay blends with a polyvinyl chloride...phenylalanine for the preparation of new poly( vinyl alcohol)= organoclay bionanocomposite films. Polym.-Plast. Technol. Eng. 2012, 51 (3), 321–327. 12. He...properties of polyvinyl chloride=acrylonitrile-butadiene- styrene. Polym.-Plast. Technol. Eng. 2012, 51 (4), 413–418. 22. Jafari, S.H.; Asadinezhad, A

  8. Warpage analysis on thin shell part using glowworm swarm optimisation (GSO)

    Science.gov (United States)

    Zulhasif, Z.; Shayfull, Z.; Nasir, S. M.; Fathullah, M.; Hazwan, M. H. M.

    2017-09-01

    The Autodesk Moldflow Insight (AMI) software was used in this study to focuses on the analysis in plastic injection moulding process associate the input parameter and output parameter. The material used in this study is Acrylonitrile Butadiene Styrene (ABS) as the moulded material to produced the plastic part. The MATLAB sortware is a method was used to find the best setting parameter. The variables was selected in this study were melt temperature, packing pressure, coolant temperature and cooling time.

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

    OpenAIRE

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

    2014-01-01

    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, respectivel...

  10. Molecular dynamics simulation aiming at interfacial characteristics of polymer chains on nanotubes with different layers

    Science.gov (United States)

    Li, Kun; Gu, Boqin; Zhu, Wanfu

    2017-03-01

    A molecular dynamics (MD) simulations study is performed on multiwalled carbon nanotubes (MWNTs)/acrylonitrile-butadiene rubber (NBR) composites. The physisorption and interfacial characteristics between the various MWNTs and polymer macromolecular chains are identified. The effects of nanotube layers on the nanotubes/polymer interactions are examined. Each of the situation result and surface features is characterized by binding energy (Eb). It is shown that the binding energy (Eb) increase with the number of layers.

  11. Mercaptosilane-assisted synthesis of sub-nanosized Pt particles within hierarchically porous ZSM-5/SBA-15 materials and their enhanced hydrogenation properties.

    Science.gov (United States)

    Gao, Daowei; Zheng, Anmin; Zhang, Xin; Sun, Hui; Dai, Xiaoping; Yang, Ying; Wang, Hai; Qin, Yuchen; Xu, Shutao; Duan, Aijun

    2015-07-07

    A novel catalyst that consists of sub-nanosized Pt particles within hierarchically porous ZSM-5/SBA-15 materials was synthesized. This catalyst exhibited high stability and a hierarchically porous structure of a micro-mesoporous composite and possessed a high density of active sites by confinement of sub-nanosized Pt particles within small-pore zeolites, showing high catalytic properties for the hydrogenation of 1,3-butadiene and cyclooctadiene at room temperature.

  12. The chemical, mechanical, and physical properties of 3D printed materials composed of TiO2-ABS nanocomposites

    OpenAIRE

    Skorski, Matthew R.; Skorski, Matthew; Esenther, Jake; Esenther, Jake M.; Ahmed, Zeeshan; Miller, Abigail E; Hartings, Matthew R.

    2016-01-01

    Abstract To expand the chemical capabilities of 3D printed structures generated from commercial thermoplastic printers, we have produced and printed polymer filaments that contain inorganic nanoparticles. TiO2 was dispersed into acrylonitrile butadiene styrene (ABS) and extruded into filaments with 1.75?mm diameters. We produced filaments with TiO2 compositions of 1, 5, and 10% (kg/kg) and printed structures using a commercial 3D printer. Our experiments suggest that ABS undergoes minor degra...

  13. Annual Report of the Inhalation Toxicology Research Institute 1991-1992

    Science.gov (United States)

    1992-12-01

    dense cellular aggregates composed mostly of lymphocytes. Accumulation of macrophages, many of which were binucleate or multinucleate giant cells ...type in the lungs. One exception to the morphologic similarities between the lesions in the two species is the rarity in the mice of Langhans giant ...Fluid: An Indicator of Type II Cell Secretions? 97 R. F. Henderson, G. C. Scott, and J. J. Waide Multidimensional HPLC Analysis of Butadiene Monoepoxide

  14. Electron spin resonance study of oriented allyl-type free radicals of butene and butadienecarboxylic acids and derivatives

    Energy Technology Data Exchange (ETDEWEB)

    Muszkat, L.

    1981-10-01

    Single-crystal electron spin resonance studies of free radicals formed by ..gamma.. irradiation were performed on a series of unsaturated carboxylic acids and their derivatives. As a rule, allyl-type extended ..pi..-electron free radicals are the most persistent species observed in the butene series molecules (2- and 3-hexenedioic acids) and in the butadiene series molecules (sorbic acid, sorbamide, and dimethyl muconate).

  15. Ni- or Cu-catalyzed cross-coupling reaction of alkyl fluorides with Grignard reagents.

    Science.gov (United States)

    Terao, Jun; Ikumi, Aki; Kuniyasu, Hitoshi; Kambe, Nobuaki

    2003-05-14

    n-Octyl fluoride underwent a cross-coupling reaction with n-propylmagnesium bromide in the presence of 1,3-butadiene using NiCl2 as a catalyst at room temperature to give undecane in moderate yields. This alkyl-alkyl cross-coupling proceeded more efficiently when CuCl2 was employed instead of NiCl2. Addition of 1,3-butadiene dramatically improved the yields of the coupling products from primary alkyl Grignard reagents in both Ni- and Cu-catalyzed reactions. Alkyl fluorides efficiently reacted with tertiary alkyl and phenyl Grignard reagents using CuCl2 in the absence of 1,3-butadiene to afford the coupling products in high yields. The competitive reaction of a mixture of alkyl halides (R-X; X = F, Cl, Br) with nC5H11MgBr showed that the reactivities of the halides increase in the order R-Cl R-F R-Br. In contrast, in the Cu-catalyzed reaction with PhMgBr, the reactivities increase in the order R-Cl R-Br R-F.

  16. [3D printing in neurosurgery: a specific model for patients with craniosynostosis].

    Science.gov (United States)

    Jiménez Ormabera, Borja; Díez Valle, Ricardo; Zaratiegui Fernández, Javier; Llorente Ortega, Marcos; Unamuno Iñurritegui, Xabier; Tejada Solís, Sonia

    Craniosynostosis is a rare condition and requires a personalised surgical approach, which is why we consider the use of 3D printed models beneficial in the surgical planning of this procedure. Acrylonitrile butadiene styrene plastic skull models were designed and printed from CT images of patients between 3 and 6 months of age with craniosynostosis of different sutures. The models were used to simulate surgical procedures. Four models of four patients with craniosynostosis were produced: two with closure of the metopic suture and two with sagittal suture closure. The mean age of the patients was 5 months (3-6m) and the mean duration of the surgery was 286min (127-380min). The acrylonitrile butadiene styrene plastic models printed for the project proved to be optimal for the simulation of craniosynostosis surgeries, both anatomically and in terms of mechanical properties and reaction to surgical instruments. 3D printers have a wide range of medical applications and they offer an easy and affordable way to produce skull models. The acrylonitrile butadiene styrene material is suitable for the production of operable bone models as it faithfully reproduces the mechanical characteristics of bone tissue. Copyright © 2017 Sociedad Española de Neurocirugía. Publicado por Elsevier España, S.L.U. All rights reserved.

  17. Spatial distribution of a midblock-associating homopolymer blended into a triblock copolymer

    Energy Technology Data Exchange (ETDEWEB)

    Lee, S.H.; Koberstein, J.T. (Univ. of Connecticut, Storrs, CT (United States). Dept. of Chemical Engineering); Quan, X. (AT T Bell Labs., Murray Hill, NJ (United States)); Gancarz, I. (Technical Univ. of Wroclaw (Poland)); Wignall, G.D. (Oak Ridge National Lab., TN (United States)); Wilson, F.C. (E.I. Du Pont de Nemours, Inc., Wilmington, DE (United States))

    1994-06-06

    The spatial distribution of midblock associating homopolymer confined within the lamellar microdomain structure of a triblock copolymer is probed with small angle neutron scattering experiments. The materials examined are poly(styrene-b-[saturated 1,2-butadiene]-b-styrene) triblock copolymers to which a low molecular weight poly(saturated 1,2-butadiene) homopolymer has been added. The butadienes are saturated with either hydrogen, deuterium, or mixtures of the two gases in order to vary their neutron scattering contrast with respect to polystyrene. The results of contrast matching experiments demonstrate that there is a strong tendency for the homopolymer to localize at the center of the midblock microdomain. Experimental scattering profiles are modeled using one-dimensional scattering density profiles in order to obtain a quantitative description of the blend morphologies. This modeling indicates that two distinct scenarios exist for homopolymer localization in a triblock copolymer: one wherein the microdomain structure contracts and a second wherein there is an expansion of the microdomain. Possible origins of this behavior are proposed on the basis of the consideration of the configuration available to the midblock sequence, that is, tie chains that traverse the midblock domain, or loops that enter and exit the midblock microdomain through the same interface.

  18. Effect of rubber polarity on selective wetting of carbon nanotubes in ternary blends

    Directory of Open Access Journals (Sweden)

    H. H. Le

    2015-11-01

    Full Text Available Based on atomic force microscopy (AFM and Fourier transform infrared spectroscopy (FTIR analysis of the rubber-filler gel (wetting concept the kinetics of selective wetting of carbon nanotubes (CNTs in ternary styrene butadiene rubber (SBR/butadiene rubber (BR/natural rubber (NR blends was qualitatively and quantitatively characterized. Almost all CNTs are found to be wetted by the non-polar NR but not by the other non-polar rubber like BR or weakly polar SBR. It was proposed that phospholipids, which are linked to the α-terminal of NR can interact with the CNT surface through cation-π interactions forming strong bonding between NR and CNTs. Using the corrected surface tension value of NR, which involves the effect of phospholipids found in our previous work the selective wetting of CNTs in ternary rubber blends can be well predicted using the Z-model for a thermodynamic equilibrium state. By replacing the non-polar BR by a polar rubber like nitrile butadiene rubber (NBR as a blend component CNTs are wetted by NBR slightly more than by NR thanks to the strong interaction between CNTs and nitrile groups of NBR. SBR remains unbound to CNTs in both blends.

  19. Factors influencing particle number concentrations, size distributions and modal parameters at a roof-level and roadside site in Leicester, UK

    Energy Technology Data Exchange (ETDEWEB)

    Agus, Emily L.; Young, David T. [Energy and Resources Research Institute, University of Leeds, LS2 9JT (United Kingdom); Lingard, Justin J.N. [Energy and Resources Research Institute, University of Leeds, LS2 9JT (United Kingdom); Institute for Atmospheric Science, School of Earth and Environment, University of Leeds, LS2 9JT (United Kingdom); Smalley, Robert J. [Energy and Resources Research Institute, University of Leeds, LS2 9JT (United Kingdom); Bureau of Meteorology Research Centre, Bureau of Meteorology, GPO Box 1289, Melbourne VIC 3001 (Australia); Tate, James E.; Goodman, Paul S. [Institute for Transport Studies, University of Leeds, LS2 9JT (United Kingdom); Tomlin, Alison S. [Energy and Resources Research Institute, University of Leeds, LS2 9JT (United Kingdom)], E-mail: A.S.Tomlin@leeds.ac.uk

    2007-11-01

    Measurements of urban particle number concentrations and size distributions in the range 5-1000 nm were taken at elevated (roof-level) and roadside sampling sites on Narborough Road in Leicester, UK, along with simultaneous measurements of traffic, NO{sub x}, CO and 1,3-butadiene concentrations and meteorological parameters. A fitting program was used to determine the characteristics of up to five modal groups present in the particle size distributions. All particle modal concentrations peaked during the morning and evening rush hours. Additional events associated with the smallest mode, that were not observed to be connected to primary emissions, were also present suggesting that this mode consisted of newly formed secondary particles. These events included peaks in concentration which coincided with peaks in solar radiation, and lower concentrations of the larger modes. Investigation into the relationships between traffic flow and occupancy indicated three flow regimes; free-flow, unstable and congested. During free-flow conditions, positive linear relationships existed between traffic flow and particle modal number concentrations. However, during unstable and congested periods, this relationship was shown to break-down. Similar trends were observed for concentrations of the gas phase pollutants NO{sub x}, CO and 1,3-butadiene. Strong linear relationships existed between NO{sub x}, CO, 1,3-butadiene concentrations, nucleation and Aitken mode concentrations at both sampling locations, indicating a local traffic related emission source. At the roadside, both nucleation and Aitken mode are best represented by a decreasing exponential function with wind speed, whereas at the roof-level this relationship only occurred for Aitken mode particles. The differing relationships at the two sampling locations are most likely due to a combination of meteorological factors and distance from the local emission source.

  20. 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.

  1. Volatile Organic Compound (VOC) Removal by Vapor Permeation at Low VOC Concentrations: Laboratory Scale Results and Modeling for Scale Up.

    Science.gov (United States)

    Rebollar-Perez, Georgette; Carretier, Emilie; Lesage, Nicolas; Moulin, Philippe

    2011-03-03

    Petroleum transformation industries have applied membrane processes for solvent and hydrocarbon recovery as an economic alternative to reduce their emissions and reuse evaporated components. Separation of the volatile organic compounds (VOCs) (toluene-propylene-butadiene) from air was performed using a poly dimethyl siloxane (PDMS)/α-alumina membrane. The experimental set-up followed the constant pressure/variable flow set-up and was operated at ~21 °C. The membrane is held in a stainless steel module and has a separation area of 55 × 10-4 m². Feed stream was set to atmospheric pressure and permeate side to vacuum between 3 and 5 mbar. To determine the performance of the module, the removed fraction of VOC was analyzed by Gas Chromatography/Flame Ionization Detector (GC/FID). The separation of the binary, ternary and quaternary hydrocarbon mixtures from air was performed at different flow rates and more especially at low concentrations. The permeate flux, permeance, enrichment factor, separation efficiency and the recovery extent of the membrane were determined as a function of these operating conditions. The permeability coefficients and the permeate flux through the composite PDMS-alumina membrane follow the order given by the Hildebrand parameter: toluene > 1,3-butadiene > propylene. The simulated data for the binary VOC/air mixtures showed fairly good agreement with the experimental results in the case of 1,3-butadiene and propylene. The discrepancies observed for toluene permeation could be minimized by taking into account the effects of the porous support and an influence of the concentration polarization. Finally, the installation of a 0.02 m2 membrane module would reduce 95% of the VOC content introduced at real concentration conditions used in the oil industry.

  2. Intake of toxic and carcinogenic volatile organic compounds from secondhand smoke in motor vehicles.

    Science.gov (United States)

    St Helen, Gideon; Jacob, Peyton; Peng, Margaret; Dempsey, Delia A; Hammond, S Katharine; Benowitz, Neal L

    2014-12-01

    Volatile organic compounds (VOC) from tobacco smoke are associated with cancer, cardiovascular, and respiratory diseases. The objective of this study was to characterize the exposure of nonsmokers to VOCs from secondhand smoke (SHS) in vehicles using mercapturic acid metabolites. Fourteen nonsmokers were individually exposed in the backseat to one hour of SHS from a smoker seated in the driver's seat who smoked three cigarettes at 20-minute intervals in a stationary car with windows opened by 10 cm. Baseline and 0- to 8-hour postexposure mercapturic acid metabolites of nine VOCs were measured in urine. Air-to-urine VOC ratios were estimated on the basis of respirable particulate matter (PM2.5) or air nicotine concentration, and lifetime excess risk (LER) of cancer death from exposure to acrylonitrile, benzene, and 1,3-butadiene was estimated for adults. The greatest increase in 0- to 8-hour postexposure concentrations of mercapturic acids from baseline was MHBMA-3 (parent, 1,3-butadiene; 2.1-fold), then CNEMA (acrylonitrile; 1.7-fold), PMA (benzene; 1.6-fold), MMA (methylating agents; 1.6-fold), and HEMA (ethylene oxide; 1.3-fold). The LER of cancer death from exposure to acrylonitrile, benzene, and 1,3-butadiene in SHS for 5 hours a week ranged from 15.5 × 10(-6) to 28.1 × 10(-6) for adults, using air nicotine and PM2.5 to predict air VOC exposure, respectively. Nonsmokers have significant intake of multiple VOCs from breathing SHS in cars, corresponding to health risks that exceed the acceptable level. Smoking in cars may be associated with increased risks of cancer, respiratory, and cardiovascular diseases among nonsmokers. ©2014 American Association for Cancer Research.

  3. Volatile Organic Compound (VOC Removal by Vapor Permeation at Low VOC Concentrations: Laboratory Scale Results and Modeling for Scale Up

    Directory of Open Access Journals (Sweden)

    Philippe Moulin

    2011-03-01

    Full Text Available Petroleum transformation industries have applied membrane processes for solvent and hydrocarbon recovery as an economic alternative to reduce their emissions and reuse evaporated components. Separation of the volatile organic compounds (VOCs (toluene-propylene-butadiene from air was performed using a poly dimethyl siloxane (PDMS/α-alumina membrane. The experimental set-up followed the constant pressure/variable flow set-up and was operated at ~21 °C. The membrane is held in a stainless steel module and has a separation area of 55 × 10−4 m². Feed stream was set to atmospheric pressure and permeate side to vacuum between 3 and 5 mbar. To determine the performance of the module, the removed fraction of VOC was analyzed by Gas Chromatography/Flame Ionization Detector (GC/FID. The separation of the binary, ternary and quaternary hydrocarbon mixtures from air was performed at different flow rates and more especially at low concentrations. The permeate flux, permeance, enrichment factor, separation efficiency and the recovery extent of the membrane were determined as a function of these operating conditions. The permeability coefficients and the permeate flux through the composite PDMS-alumina membrane follow the order given by the Hildebrand parameter: toluene > 1,3-butadiene > propylene. The simulated data for the binary VOC/air mixtures showed fairly good agreement with the experimental results in the case of 1,3-butadiene and propylene. The discrepancies observed for toluene permeation could be minimized by taking into account the effects of the porous support and an influence of the concentration polarization. Finally, the installation of a 0.02 m2 membrane module would reduce 95% of the VOC content introduced at real concentration conditions used in the oil industry.

  4. Influence of Layer Thickness and Raster Angle on the Mechanical Properties of 3D-Printed PEEK and a Comparative Mechanical Study between PEEK and ABS

    Science.gov (United States)

    Wu, Wenzheng; Geng, Peng; Li, Guiwei; Zhao, Di; Zhang, Haibo; Zhao, Ji

    2015-01-01

    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. PMID:28793537

  5. Air quality in the Industrial Heartland of Alberta, Canada and potential impacts on human health

    Science.gov (United States)

    Simpson, Isobel J.; Marrero, Josette E.; Batterman, Stuart; Meinardi, Simone; Barletta, Barbara; Blake, Donald R.

    2015-01-01

    The “Industrial Heartland” of Alberta is Canada’s largest hydrocarbon processing center, with more than 40 major chemical, petrochemical, and oil and gas facilities. Emissions from these industries affect local air quality and human health. This paper characterizes ambient levels of 77 volatile organic compounds (VOCs) in the region using high-precision measurements collected in summer 2010. Remarkably strong enhancements of 43 VOCs were detected, and concentrations in the industrial plumes were often similar to or even higher than levels measured in some of the world’s largest cities and industrial regions. For example maximum levels of propene and i-pentane exceeded 100 ppbv, and 1,3-butadiene, a known carcinogen, reached 27 ppbv. Major VOC sources included propene fractionation, diluent separation and bitumen processing. Emissions of the measured VOCs increased the hydroxyl radical reactivity (kOH), a measure of the potential to form downwind ozone, from 3.4 s−1 in background air to 62 s−1 in the most concentrated plumes. The plume value was comparable to polluted megacity values, and acetaldehyde, propene and 1,3-butadiene contributed over half of the plume kOH. Based on a 13-year record (1994–2006) at the county level, the incidence of male hematopoietic cancers (leukemia and non-Hodgkin lymphoma) was higher in communities closest to the Industrial Heartland compared to neighboring counties. While a causal association between these cancers and exposure to industrial emissions cannot be confirmed, this pattern and the elevated VOC levels warrant actions to reduce emissions of known carcinogens, including benzene and 1,3-butadiene. PMID:25685050

  6. Influence of Layer Thickness and Raster Angle on the Mechanical Properties of 3D-Printed PEEK and a Comparative Mechanical Study between PEEK and ABS.

    Science.gov (United States)

    Wu, Wenzheng; Geng, Peng; Li, Guiwei; Zhao, Di; Zhang, Haibo; Zhao, Ji

    2015-09-01

    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.

  7. Warpage analysis on thin shell part using response surface methodology (RSM)

    Science.gov (United States)

    Zulhasif, Z.; Shayfull, Z.; Nasir, S. M.; Fathullah, M.; Hazwan, M. H. M.

    2017-09-01

    The optimisation of moulding parameters appropriate to reduce warpage defects produce using Autodesk Moldflow Insight (AMI) 2012 software The product is injected by using Acrylonitrile-Butadiene-Styrene (ABS) materials. This analysis has processing parameter that varies in melting temperature, mould temperature, packing pressure and packing time. Design of Experiments (DOE) has been integrated to obtain a polynomial model using Response Surface Methodology (RSM). The Glowworm Swarm Optimisation (GSO) method is used to predict a best combination parameters to minimise warpage defect in order to produce high quality parts.

  8. 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.

  9. Levels of selected urinary metabolites of volatile organic compounds among children aged 6-11 years.

    Science.gov (United States)

    Jain, Ram B

    2015-10-01

    Data from National Health and Nutrition Examination Survey for the years 2011-2012 were used to evaluate variability in the observed levels of 20 urinary metabolites of volatile organic compounds (VOCs) by age, gender, and race/ethnicity among children aged 6-11 years. Exposure to environmental tobacco smoke was positively associated with the levels of selected metabolites of acrylonitrile, 1,3-butadiene, cyanide, and propylene oxide in a dose-response manner. Levels of the selected metabolites of acrolein, acrylonitrile, 1,3-butadiene, styrene, toluene, and xylene decreased with increase in age. Levels of 1-bromopropane decreased with number of rooms in the house but the reverse was true for 1,3-butadiene, carbon-disulfide, and N,N-dimethylformamide. Levels of most of the 20 metabolites did not vary with gender. Non-Hispanic white children had higher adjusted levels of N-Acetyl-S-(3,4-dihydroxybutyl)-L-cysteine (DHBMA), N-Acetyl-S-(N-methylcarbamoyl)-L-cysteine (AMCC), and phenylglyoxylic acid (PGA) than non-Hispanic black children. Non-Hispanic white children had statistically significantly higher adjusted levels of N-Acetyl-S-(2-carbamoyl-2-hydroxyethyl)-L-cysteine (GAMA), trans, trans-Muconic acid (MU), and N-Acetyl-S-(N-methylcarbamoyl)-L-cysteine (AMCC) than non-Hispanic Asian children but statistically significantly lower levels of N-Acetyl-S-(n-propyl)-L-cysteine (BPMA) than non-Hispanic Asian children. Non-Hispanic Asian children had the lowest levels of 13 of the 20 metabolites among four major racial/ethnic groups but highest levels for three metabolites. For selected metabolites of acrolein, acrylamide, acrylonitrile-vinyl chloride-ethylene oxide, benzene, 1,3-butadien, crotonaldehyde, cyanide, ethylbenzene-styrene, and toluene, children had statistically significantly higher levels than nonsmoking adults. These results demonstrate how vulnerable children are to being exposed to harmful chemicals like VOCs in their own homes. Copyright © 2015 Elsevier

  10. 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.

  11. Hydrothermal Synthesis of Bi2S3 Nanostructures and ABS-Based Polymeric Nanocomposite

    Directory of Open Access Journals (Sweden)

    D. Ghanbari

    2014-04-01

    Full Text Available Bismuth sulfide nano-rods and nano-flowers were synthesized via a hydrothermal reaction at a relatively low temperature. Thioglycolic acid is used as sulfur source and capping agent simultaneously. Bi2S3 nanostructures were then added to acrylonitrile-butadiene-styrene (ABS copolymer. The thermal stability behavior of ABS filled with bismuth sulfide nano-rods were investigated by thermogravimetric analysis (TGA. Nanostructures were characterized by X-ray diffraction (XRD, scanning electron microscopy (SEM and atomic force microscopy (AFM. The flame retardancy behavior of ABS-Bi2S3 was studied by UL-94 analysis.

  12. 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.

  13. Magnetron reactively sputtered Ti-DLC coatings on HNBR rubber: The influence of substrate bias

    OpenAIRE

    Bui, X.L.; Pei, Y.T.; De Hosson, J. Th. M.

    2008-01-01

    In this study, Ti-containing diamond-like carbon (Ti-DLC) coatings have been deposited on HNBR (hydrogenated nitrile butadiene) rubber and also on Si wafer as reference via unbalanced magnetroli reactive sputtering from a Ti target in C2H2/Ar plasma. The deposition rates of coatings on rubber and Si wafer were about the same. Columnar structures resulting from a rough interface were often observed in the coatings deposited on rubbers. Only at a high bias voltage of -300 V the coating on HNBR ...

  14. Studies on the rubber phase stability in gamma irradiated polystyrene-SBR blends by using FT-IR and Raman spectroscopy[Gamma irradiation; Polystyrene-SBR blends; Izod impact; FTIR; Raman

    Energy Technology Data Exchange (ETDEWEB)

    Martinez-Barrera, G.; Lopez, H.; Castano, V.M.; Rodriguez, R. E-mail: rogelior@servidor.unam.mx

    2004-02-01

    Improvement in the impact properties of polystyrene-SBR blends produced by different concentrations and types of styrene-butadiene rubber (SBR) was studied. The samples were gamma irradiated at different doses to achieve good adhesion, and consequently good stability, between the rubbery phase and the polystyrene matrix, producing an improvement in the impact properties. The results show that the best Izod impact was obtained for a blend with 10% SBR and with a dose of 100 kGy. Several samples with 0%, 3%, 5% and 10% of SBR were prepared and characterized by FT-IR and FT-Raman spectroscopies.

  15. Effect of silica fume and SBR latex on the pasteaggregate interfacial transition zone

    Directory of Open Access Journals (Sweden)

    João Adriano Rossignolo

    2007-03-01

    Full Text Available This paper deals with the effect of silica fume and styrene-butadiene latex (SBR on the microstructure of the interfacial transition zone (ITZ between Portland cement paste and aggregates (basalt. Scanning Electron Microscope (SEM equipped with energy dispersive x ray analysis system (EDX was used to determine the ITZ thickness. In the plain concrete a marked ITZ around the aggregate particles (55 µm was observed, while in concretes with silica fume or latex SBR the ITZ was less pronounced (35-40 µm. However, better results were observed in concretes with silica fume and latex SBR (20-25 µm.

  16. Evolution of the crosslink structure in the elastomers NR and SBR

    Energy Technology Data Exchange (ETDEWEB)

    Salgueiro, W. [IFIMAT-UNCentro and CICPBA, Pinto 399, B7000GHG Tandil (Argentina)]. E-mail: wsalgue@exa.unicen.edu.ar; Somozaa, A. [IFIMAT-UNCentro and CICPBA, Pinto 399, B7000GHG Tandil (Argentina); Marzocca, A.J. [LPMPyMC, Depto. de Fisica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pabellon I, 1428 Buenos Aires (Argentina); Consolati, G. [Dipartimento di Fisica, Politecnico di Milano, Piazza Leonardo da Vinci 32, I-20133 Milan (Italy); Quasso, F. [Dipartimento di Fisica, Politecnico di Milano, Piazza Leonardo da Vinci 32, I-20133 Milan (Italy)

    2007-02-15

    An experimental positron annihilation lifetime spectroscopy (PALS), differential scanning calorimetry (DSC) and small angle X-ray scattering (SAXS) study of the effect of the advance of the crosslinking reaction on the free volume in a copolymer of styrene-butadiene and natural rubbers was carried out. The crosslink density developed in SBR specimens with different sulfur contents and cure temperatures was studied. SAXS technique was applied to study the process of crosslinking in NR as a function of the cure temperature. Finally, a study of different SBR/NR blends is presented using PALS and DSC.

  17. Evolution of the crosslink structure in the elastomers NR and SBR

    Science.gov (United States)

    Salgueiro, W.; Somozaa, A.; Marzocca, A. J.; Consolati, G.; Quasso, F.

    2007-02-01

    An experimental positron annihilation lifetime spectroscopy (PALS), differential scanning calorimetry (DSC) and small angle X-ray scattering (SAXS) study of the effect of the advance of the crosslinking reaction on the free volume in a copolymer of styrene-butadiene and natural rubbers was carried out. The crosslink density developed in SBR specimens with different sulfur contents and cure temperatures was studied. SAXS technique was applied to study the process of crosslinking in NR as a function of the cure temperature. Finally, a study of different SBR/NR blends is presented using PALS and DSC.

  18. Devulcanization of styrenebutadiene (SBR waste tire by controlled oxidation

    Directory of Open Access Journals (Sweden)

    Rios Rachel R.V.A.

    2006-01-01

    Full Text Available This work describes the devulcanization of vulcanized SBR (Styrene Butadiene Rubber based on controlled oxidation with nitric acid. IR, ¹H and 13C-NMR, CHN elemental analyses, TG, GPC and TPD-MS (Temperature Programmed Decomposition-Mass Spectrometry experiments suggest that nitric acid promotes two processes: (i devulcanization by oxidation of the sulfide crosslinks and (ii oxidation of the carbon framework leading to the formation of -COOH and -NO2 groups. Under aggressive conditions (HNO3, reflux the polymer chain is strongly oxidized and fragmented to a highly oxygenated low molecular weight fraction, which is soluble in water.

  19. Electronic states of model hydrocarbon chromophores investigated by Synchrotron Radiation Linear Dichroism (SRLD) spectroscopy on aligned samples

    DEFF Research Database (Denmark)

    Nguyen, Duy Duc; Hoffmann, Søren Vrønning; Jones, Nykola

    2010-01-01

    Conventional UV-VIS absorption spectroscopy provides information on transition energies and intensities. Linear dichroism (LD) spectroscopy on aligned molecular samples yields additional information on transition moment directions, thereby frequently leading to resolution of otherwise overlapping...... for four hydrocarbons which are of interest as model compounds for molecular wires and switches: 1)  Diphenylethyne (tolane, DPA) 2)  1,4-Bis(phenylethynyl)benzene (BPEB) 3)  (E)-1,2-Diphenylethene (stilbene, DPE) 4)  (E,E’)-1,4-Diphenyl-1,3-butadiene (DPB)...

  20. Triplet State Resonance Raman Spectrum of all-trans-diphenylbutadiene

    DEFF Research Database (Denmark)

    Wilbrandt, Robert Walter; Grossman, W.E.L.; Killough, P.M

    1984-01-01

    The resonance Raman spectrum of all-trans-diphenylbutadiene (DPB) in its ground state and the resonance Raman spectrum (RRS) of DPB in its short-lived electronically excited triplet state are reported. Transient spectra were obtained by a pump-probe technique using two pulsed lasers....... The preresonance spectrum of the ground state is not significantly changed from that of the nonresonance spectrum. In the resonance spectrum of the triplet state the double-bond stretching mode of the butadiene part is shifted by 43 cm-1 downward to 1582 cm-1 whereas the single-bond stretching mode is essentially...