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Sample records for acrylonitrile butadiene styrene

  1. 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.

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

    OpenAIRE

    McCulley, Jonathan M.

    2013-01-01

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

  3. 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.

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

    Directory of Open Access Journals (Sweden)

    Aboulfazl Barati

    2012-01-01

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

  5. 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.

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

    Institute of Scientific and Technical Information of China (English)

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

    2003-01-01

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

  7. 21 CFR 177.1030 - Acrylonitrile/butadiene/styrene/methyl methacrylate copolymer.

    Science.gov (United States)

    2010-04-01

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

  8. 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.

  9. 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.

  10. 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.

  11. 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.

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

    Institute of Scientific and Technical Information of China (English)

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

    2008-01-01

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

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

    Science.gov (United States)

    McCulley, Jonathan M.

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

  14. 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.

  15. 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

  16. 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.

  17. 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.

  18. 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.

  19. 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.

  20. 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.

  1. 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.

  2. 21 CFR 177.1020 - Acrylonitrile/butadiene/sty-rene co-polymer.

    Science.gov (United States)

    2010-04-01

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

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

    Institute of Scientific and Technical Information of China (English)

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

    2011-01-01

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

  4. 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.

  5. 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.

  6. 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.

  7. 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.

  8. 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.

  9. 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.

  10. 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.

  11. Ionizing radiation effect study by electron beam on acrylonitrile butadiene styrene - ABS terpolymer; Estudo do efeito da radiacao ionizante por feixe de eletrons sobre o terpolimero acrilonitrila butadieno estireno -ABS

    Energy Technology Data Exchange (ETDEWEB)

    Landi, Tania Regina Lourenco

    2003-07-01

    The great advantage in the researches involving development has as objective to increase significantly the quality of the products. The ABS (acrylonitrile, butadiene, styrene) resins are terpolymers formed by an elastomer and two thermoplastics amorphous components. The three different monomeric units from the terpolymer ABS contribute separately to the material characteristics exhibited. The molecular stiffness originating from polystyrene and the benzene ring hanging on the chain is responsible for the flexion module ABS. The acrylonitrile and the styrene incorporated butadiene exercises strong influence in the resistance to the impact because it reduces the bonding among them. The engineering use of this terpolymer became important due their mechanical properties and mainly, for the responses of this to tensions or deformations applied. The polymeric materials, when submitted to the ionizing radiation are modified by the transference of energy to these materials, introducing excitation and ionization of the molecules, generating chemical reactions that can produce permanent modifications in the polymeric physicochemical structure. The induced modifications can result in the polymeric material degradation or crosslinking, which can result in the improvement of some properties. This work has, as objective, to study the electron beam ionizing radiation effect, at different doses, in the properties of the polymer ABS. The studied properties were: tensile strength at break, elongation at break, Izod impact strength, flexural strength, melt flow index, Vicat softening temperature and the thermic distortion temperature. Also researches on Differential Scanning Calorimetry (DSC) and Thermogravimetric Analyses (TGA) were accomplished. From the experimental results, it was showed that for doses until 500 kGy, at 22.6 kGy/s dose rate, in the presence of air, the crosslinking process of ABS prevails. (author)

  12. Blends of Styrene-Butadiene-Styrene Triblock Copolymer with Random Styrene-Maleic Anhydride Copolymers

    NARCIS (Netherlands)

    Piccini, Maria Teresa; Ruggeri, Giacomo; Passaglia, Elisa; Picchioni, Francesco; Aglietto, Mauro

    2002-01-01

    Blends of styrene-butadiene-styrene triblock copolymer (SBS) with random styrene-maleic anhydride copolymers (PS-co-MA), having different MA content, were prepared in a Brabender Plastigraph mixer. The presence of polystyrene (PS) blocks in the SBS copolymer and the high styrene content (93 and 86 w

  13. Rheological properties of styrene butadiene styrene polymer modified road bitumens

    Energy Technology Data Exchange (ETDEWEB)

    Gordon D. Airey [University of Nottingham, Nottingham (United Kingdom). Nottingham Centre for Pavement Engineering, School of Civil Engineering

    2003-10-01

    The use of polymers for the modification of bitumen in road paving applications has been growing rapidly over the last decade as government authorities and paving contractors seek to improve road life in the face of increased traffic. Currently, the most commonly used polymer for bitumen modification is the elastomer styrene butadiene styrene (SBS) followed by other polymers such as styrene butadiene rubber, ethylene vinyl acetate and polyethylene. This paper describes the polymer modification of two penetration grade bitumens with SBS. Six polymer modified bitumens (PMBs) were produced by mixing the bitumens from two crude oil sources with a linear SBS copolymer at three polymer contents. The rheological characteristics of the SBS PMBs were analysed by means of conventional as well as dynamic mechanical analysis using a dynamic shear rheometer (DSR). The results of the investigation indicate that the degree of SBS modification is a function of bitumen source, bitumen polymer compatibility and polymer concentration, with the higher polymer concentrations in a high aromatic content bitumen producing a highly elastic network which increases the viscosity, complex modulus and elastic response of the PMB, particularly at high service temperatures. However, ageing of the SBS PMBs tends to result in a reduction of the molecular size of the SBS copolymer with a decrease in the elastic response of the modified road bitumen. 25 refs., 11 figs., 6 tabs.

  14. Oil Gels Based on Styrene Butadiene Rubber

    Institute of Scientific and Technical Information of China (English)

    ZHOU Mei-hua (周美华); XU Jing-bo(徐静波); Won-jei CHO

    2004-01-01

    Four oil absorbents based on styrene butadiene (SBR),i. e., pure SBR (PS), 4- tert-butylstyrene-SBR (PBS),EPDM-SBR network (PES) and 4-tert-butylstyrene-EPDMSBR ( PBES ), were produced from crosslinking polymerization of uncured styrene butadiene rubber (SBR),4- tert-butylstyrene ( tBS ) and ethylene-propylene-diene terpolymer (EPDM). The reaction took place in toluene using benzoyl peroxide (BPO) as an initiator. Uncured SBR was used as both a pre-polymer and a crosslink agent in this work, and the crosslinked polymer was identified by IR spectroscopy. The oil absorbency of the crosslinked polymer was evaluated with the method ASTM (F726 - 81). The order of maximum oil absorbency was PBES > PBS >PES > PS. The maximum values of oil absorbency of PBES and PBS were 74.0g/g and 69.5g/g, respectively. Gel fractions and swelling kinetic constants, however, had the opposite sequences. The swelling kinetic constant of PS evaluated by an experimental equation was 49. 97 ×10-2h-1.

  15. Blending of styrene-block-butadiene-block-styrene copolymer with sulfonated vinyl aromatic polymers

    OpenAIRE

    Ruggeri, Giacomo; Passaglia, Elisa; Giorgi, Ivan; Picchioni, Francesco; Aglietto, Mauro

    2001-01-01

    Different polymers containing sulfonic groups attached to the phenyl rings were prepared by sulfonation of polystyrene (PS) and styrene-block-(ethylene-co-1-butene)-block-styrene (SEBS). The sulfonation degree (SD) was varied between 1 and 20 mol% of the styrene units. Polyphase materials containing sulfonated units were prepared by blending styrene-block-butadiene-block-styrene (SBS), with both sulfonated PS and sulfonated SEBS in a Brabender mixer. Such a procedure was performed as an alter...

  16. 21 CFR 181.32 - Acrylonitrile copolymers and resins.

    Science.gov (United States)

    2010-04-01

    ... paragraph (b) of this section, may be safely used as follows: (1) Films. (i) Acrylonitrile/butadiene/styrene.../styrene copolymer—no restrictions. (2) Coatings. (i) Acrylonitrile/butadiene copolymer blended with... Paint Branch Pkwy., College Park, MD 20740, or available for inspection at the National Archives and...

  17. 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.

  18. Genetic toxicity of 1,3-butadiene and styrene.

    Science.gov (United States)

    Norppa, H; Sorsa, M

    1993-01-01

    1,3-Butadiene and styrene (vinyl benzene) are indirect genotoxins, which require metabolic activation to an epoxide form in order to bind covalently to DNA. Styrene 7,8-oxide, the active metabolite of styrene, is a carcinogen in rodents and has been shown to be genotoxic in most in-vitro test systems and at various genetic endpoints. The few studies available on the genotoxicity of styrene 7,8-oxide in vivo have yielded negative or (in mice) weakly positive results. Styrene is not usually genotoxic in vitro in assays employing a microsomal preparation from rat liver for metabolic activation, but positive effects have been obtained when other sources of metabolic activation, such as human erythrocytes, were provided. In vivo, styrene has been found repeatedly to be weakly genotoxic in the assay for sister chromatid exchange, especially in mice. Cytogenetic damage (usually chromosomal aberrations) has been reported in many studies of workers, mainly from the reinforced plastics industry where ambient concentrations of styrene may be high (50-100 ppm), while most negative findings are associated with exposure to lower levels. Butadiene is metabolized to two reactive forms, 1,2-epoxy-3-butene and further to 1,2:3,4-diepoxybutane, both of which are genotoxic in various test systems in vitro. The lowest effective dose of the latter is 1-2 orders of magnitude higher than that of the respective monoepoxide. Butadiene itself has not been tested extensively for genotoxicity in vitro. A species-specific difference in the responses of mice and rats at various cytogenetic end-points is seen in vivo, the lowest effective concentrations in rats being clearly higher than those in mice.(ABSTRACT TRUNCATED AT 250 WORDS)

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

    Science.gov (United States)

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

    2010-06-01

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

  20. Perinatal Toxicity and Carcinogenicity Studies of StyreneAcrylonitrile Trimer, A Ground Water Contaminant

    OpenAIRE

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

    2013-01-01

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

  1. Study on the thermal stability of styrene butadiene rubber nanocomposites

    Science.gov (United States)

    Saeb, M. R.; Chenari, T. N.; Parast, O. Yazdan; Jafari, B.; Asadi, H.; Safari, M. Arfavi; Holisaz, H.

    2012-07-01

    This study aims to investigate the thermal stability of the styrene butadiene rubber (SBR) nanocomposites containig surface modified calcium carbonate (MCC). All nanocomposites were produced at various nanofiller contents, utilizing a laboratory scale two-roll mill. The thermal stability parameters including initial decomposing temperature, temperature at maximum rate of weight loss, and char content of the MCC/SBR nanocomposites were then compared. It was found that by increasing the filler content, the decomposition temperature of MCC/SBR nanocomposites increases. Furthermore, the char content at high temperatures rises by increasing nanofiller content.

  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. Durability of styrene-butadiene latex modified concrete

    Energy Technology Data Exchange (ETDEWEB)

    Shaker, F.A.; El-Dieb, A.S.; Reda, M.M. [Ain Shams Univ., Cairo (Egypt). Dept. of Structural Engineering

    1997-05-01

    The durability of reinforced concrete structures represents a major concern to many investigators. The use of latex modified concrete (LMC) in construction has urged researchers to review and investigate its different properties. This study is part of a comprehensive investigation carried on the use of polymers in concrete. The main objective of this study to investigate and evaluate the main durability aspects of Styrene-Butadiene latex modified concrete (LMC) compared to those of conventional concrete. Also, the main microstructural characteristics of LMC were studied using a Scanning Electron Microscope (SEM). The SEM investigation of the LMC showed major differences in its microstructure compared to that of the conventional concrete. The LMC proved to be superior in its durability compared to the durability of conventional concrete especially its water tightness (measured by water penetration, absorption, and sorptivity tests), abrasion, corrosion, and sulphate resistance.

  4. Carbon nanotubes as reinforcement of styrene-butadiene rubber

    Energy Technology Data Exchange (ETDEWEB)

    De Falco, Alejandro [Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Fisica, LPMPyMC, Pabellon 1, Buenos Aires 1428 (Argentina); Goyanes, Silvia [Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Fisica, LPMPyMC, Pabellon 1, Buenos Aires 1428 (Argentina); Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) (Argentina)], E-mail: goyanes@df.uba.ar; Rubiolo, Gerardo H. [Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Fisica, LPMPyMC, Pabellon 1, Buenos Aires 1428 (Argentina); Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) (Argentina); Departamento de Materiales, CNEA, Av. del Libertador 8250, Buenos Aires 1424 (Argentina); Mondragon, Inaki [Materials and Technologies Group, Escuela Univ. Politecnica, Dpto. Ingenieria Quimica y M. Ambiente, Universidad Pais Vasco, Pza. Europa 1, 20018 Donostia-San Sebastian (Spain); Marzocca, Angel [Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Fisica, LPMPyMC, Pabellon 1, Buenos Aires 1428 (Argentina)

    2007-10-31

    This study reports an easy technique to produce cured styrene-butadiene rubber (SBR)/multi-walled carbon nanotubes (MWCNT) composites with a sulphur/accelerator system at 150 deg. C. Significant improvement in Young's modulus and tensile strength were achieved by incorporating 0.66 wt% of filler without sacrificing SBR elastomer high elongation at break. A comparison with carbon black filled SBR was also made. Field emission scanning electron microscopy was used to investigate dispersion and fracture surfaces. Results indicated that the homogeneous dispersion of MWCNT throughout SBR matrix and strong interfacial adhesion between oxidized MWCNT and the matrix are responsible for the considerable enhancement of mechanical properties of the composite.

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

    Institute of Scientific and Technical Information of China (English)

    HAN Xiaozu; LI Shaoying; ZHANG Qingyu

    1990-01-01

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

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

    OpenAIRE

    Mirosława Prochoń; Anita Przepiórkowska

    2013-01-01

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

  7. Evaluation of tri-steps modified styrene-butadiene-styrene block copolymer membrane for wound dressing

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Jen Ming, E-mail: jmyang@mail.cgu.edu.tw; Huang, Huei Tsz

    2012-08-01

    Tri-steps modified styrene-butadiene-styrene block copolymer (SBS) membrane was prepared with epoxidation, ring opening reaction with maleated ionomer and layer-by-layer assembled polyelectrolyte technique. The tri-steps modified SBS membrane was characterized by infrared spectroscopy and X-ray photoelectron spectroscope (XPS). The structures of the modified SBS membranes were identified with methylene blue and azocarmine G. The content of amino group on the surface of the modified membrane was calculated from uptake of an acid dye. The values of the contact angle, water absorption, water vapor transmission rate and the adsorption of fibronectin on the membranes were determined. To evaluate the biocompatibility of the tri-steps modified SBS membrane, the cytotoxicity, antibacterial and growth profile of the cell culture of 3T3 fibroblasts on the membrane were evaluated. The bactericidal activity was found on the modified SBS. From the cell culture of 3T3 fibroblasts on the membrane, it revealed that the cells not only remained viable but also proliferated on the surface of the tri-steps modified SBS membranes. As the membranes are sterile semipermeable with bactericidal activity and transparent allowing wound checks, they can be considered for shallow wound with low exudates. - Highlights: Black-Right-Pointing-Pointer Styrene-butadiene-styrene block copolymer (SBS) was modified with tri-steps. Black-Right-Pointing-Pointer The tri-steps are epoxidation, ring opening reaction and layer-by-layer assembly. Black-Right-Pointing-Pointer Modified SBS membrane for wound dressing is evaluated. Black-Right-Pointing-Pointer Membranes are sterile semipermeable with bactericidal activity and transparent. Black-Right-Pointing-Pointer Membranes can be considered for shallow wound with low exudates.

  8. Preparation of anionically polymerized butadiene-co-styrene copolymer-multiwalled carbon nanotubes nanocomposites

    Institute of Scientific and Technical Information of China (English)

    Zhong Guang; Wang, Jing Hua; Ling Xu

    2012-01-01

    Poly(butadiene-co-styrene) copolymer/multi-walled carbon nanotubes (SB-MWNTs) nanocomposites are prepared via terminating anionically synthesized living poly(butadiene-styryl)lithium with acyl chlorides on the MWNTs,which obtained from the carboxylation and acylation of the MWNTs.Results from the characterization of the SB-MWNTs nanocomposites,including its soluble in solvent,UV-vis and TEM of the dissolved samples,TGA and SEM of nanocomposites are presented and discussed respectively.MWNTs treated by SB can be easily distributed in the SBR (styrene-butadiene rubber) matrix.

  9. 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.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1983-12-01

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

  11. EFFECTS OF STYRENE-BUTADIENE-STYRENE ON STIFFNESS OF ASPHALT CONCRETE AT DIFFERENT TRAFFIC CONDITIONS

    Directory of Open Access Journals (Sweden)

    GHOLAMALI SHAFABAKHSH

    2016-04-01

    Full Text Available The previous studies have explored the effects of Styrene-Butadiene-Styrene (SBS as the most prevalent modifier for asphalt mixtures. The current study intends to compare stiffness modulus of control and SBS modified asphalt mixtures under different traffic loadings. To this end, resilient modulus tests were performed on both conventional and SBS modified specimens. Tests were conducted at 5, 25 and 40°C with loading times of 50, 100, 300, 600 and 1000 milliseconds and 4, 9 and 30 as ratio of rest periods (between loading pulses to loading times (R/L. Using these test parameters and haversine and square loading pulses that represent vertical stress distribution at different depths within an asphalt layer, a variety of traffic densities and vehicle speeds were simulated and their effects on stiffness of asphalt concrete were determined. Results indicated that SBS modification provide higher stiffness under haversine pulse with long loading time at 40°C, so that it was about 3 times of unmodified mixture stiffness. The effect of traffic density that represented by R/L was significant only in long loading time (1000 ms especially under haversine pulse.

  12. Radiation-induced crosslinking of poly(styrene-butadiene-styrene) block copolymers and their sulfonation

    Science.gov (United States)

    Lee, Sun-Young; Song, Ju-Myung; Sohn, Joon-Yong; Shul, Yong-Gun; Shin, Junhwa

    2013-12-01

    Several crosslinked poly(styrene-butadiene-styrene) (c-SBS) block copolymer films were prepared using a gamma ray or electron beam with various irradiation doses and the prepared c-SBS film was then subjected to sulfonation using a chlorosulfonic acid (CSA) solution to introduce a sulfonic acid group. To estimate the degree of crosslinking, the gel fractions and FT-IR spectra of the c-SBS films were used and the results indicate that the degree of crosslinking is increased with an increase in the radiation dose. The surface morphology and mechanical property of the c-SBS films were observed using SEM and UTM instruments, respectively. The sulfonated c-SBS films were investigated by measuring the ion exchange capacity (IEC) and by observing the cross-sectional distribution patterns of sulfonic acid group using an SEM-EDX instrument. The IEC and SEM-EDX studies indicate that the sulfonated c-SBS membranes can be successfully prepared through the radiation crosslinking of the SBS film and the subsequent sulfonation with a diluted CSA solution.

  13. Analysis of styrene-butadiene-styrene polymer modified bitumen using fluorescent microscopy and conventional test methods.

    Science.gov (United States)

    Sengoz, Burak; Isikyakar, Giray

    2008-01-31

    This paper presents a laboratory study of modified bitumen containing styrene-butadiene-styrene (SBS) copolymer. Polymer modified bitumen (PMB) samples have been produced by mixing a 50/70 penetration grade unmodified (base) bitumen with SBS Kraton D1101 copolymer at five different polymer contents. The fundamental characteristics of the SBS PMB samples have been determined using conventional methods. The morphology of the samples as well as the percent area (%) distribution of SBS polymers throughout the base bitumen have been characterized and determined by means of fluorescence microscopy and Qwin Plus image analysis program, respectively. The mechanical properties of the hot-mix asphalt (HMA) containing SBS PMBs have also been analyzed and compared with HMA incorporating base bitumen. The effect of polymer addition on the short and long term aging characteristics of HMA have been evaluated by indirect tensile strength (ITS) test. The results indicated that polymer modification improved the conventional properties (penetration, softening point, etc.) and the mechanical properties (Marshall, ITS, etc.) of the base bitumen. It was also concluded that at low polymer contents, the samples revealed the existence of dispersed polymer particles in a continuous bitumen phase, whereas at high polymer contents a continuous polymer phase has been observed. Moreover, it was found out that the polymer addition minimizes the short and long term aging of HMA.

  14. Influence of styrene-butadiene-styrene polymer modification on bitumen viscosity

    Energy Technology Data Exchange (ETDEWEB)

    Lu, X.; Isacsson, U. [Royal Institute of Technology, Stockholm (Sweden). Division of Highway Engineering

    1997-11-01

    It is reported that the effects of polymer content/structure and bitumen type on viscosity characteristics of styrene-butadiene-styrene (SBS) polymer modified bitumens were investigated. The study indicated that SBS polymers were not inert additives and increases in kinematic and dynamic viscosities of the modified bitumens were not directly proportional to polymer content; a marked viscosity increase was observed when the polymer content increased from 3 to 6% by weight of the blend. Modification with a sufficiently high polymer content also increased the degree of non-Newtonian behaviour of the bitumens. The base bitumens and modified bitumens containing 3% SBS were observed to be essentially shear rate independent, while those containing 6 to 9% SBS displayed shear-thinning behaviour. Compared to the modified bitumens with linear SBS, the modified bitumens with branched SBS demonstrated a higher degree of shear-thinning behaviour. These effects were dependent on ranges of shear rate and temperature. The increased degree of non-Newtonian behaviour was observed to influence the correlations between kinematic and dynamic viscosities. 12 refs., 7 figs., 2 tabs.

  15. 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.

  16. Synthesis And Properties Of Functional Ultra-High Molecular Weight Transparent Styrene-Butadiene Block Copolymer

    Institute of Scientific and Technical Information of China (English)

    GONG Guang-bi; ZHAO Xu-tao; WANG Gui-lun

    2004-01-01

    Functional ultra-high molecular weight transparent styrene-butadiene block copolymer possesses both high transparency and impact resistance and has excellent comprehensive properties prior to other transparent resins. In this paper we not only use anionic polymerization process which includes 1 time addition of initiator and 3 time addition of monomers, but also introduce functional coupling agent for the fist time to prepare mentioned functional block copolymer.The typical preparation process is described as the following: (a) Adding cyclohexane, styrene and initiator to the polymerizer, the polymerization is carried out at 50~75℃; (b) adding a mixture of styrene, butadiene and cyclohexane, the polymerization is carried out at 50~70℃ ;(c) adding a mixture of butadiene and cyclohexane, the polymerization is finished at 60~70℃ ;(d) adding coupling agent which is a substituted trimethoxysilane being expressed as N-silane, O-silane and being converted into a functional group (-NH, -OH) of mentioned block copolymer, coupling at 75~90℃ for 1 hr; (e) The amounts of coupling agent are about one sixth to one third of the initiator; (f) treating the prepared copolymer solution with some water and Carbon dioxide at 50~70℃ for 15 min.The copolymer is from three-arm to six-arm mono-modal radial block copolymer having 75~90%styrene, 10~25% butadiene and functional group of-NH or-OH. of the copolymer, Mw is from 30×104 to 120×104, Mw/Mn from 2.0 to 2.5, Izod notched impact strength 50~65 J/m,light transmission not less 87.5%, tensile strength not less 45 Mpa.The exploratory research shows that the mole ratio and feed rate of the random copolymerized styrene-butadiene, as well as the total ratio of styrene-butadiene have greater influence on the properties of the copolymer. The following model is established:Y=bo +∑3j=1 bjxj+∑3j=1bkjxkxj+∑3j=1bjjx2j (k<j)Where: Y is the light transmission, tensile strength, elongation, Izod notched impact

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

    OpenAIRE

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

    2012-01-01

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

  18. 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.

  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. Blending of styrene-block-butadiene-block-styrene copolymer with sulfonated vinyl aromatic polymers

    NARCIS (Netherlands)

    Ruggeri, Giacomo; Passaglia, Elisa; Giorgi, Ivan; Picchioni, Francesco; Aglietto, Mauro

    2001-01-01

    Different polymers containing sulfonic groups attached to the phenyl rings were prepared by sulfonation of polystyrene (PS) and styrene-block-(ethylene-co-1-butene)-block-styrene (SEBS). The sulfonation degree (SD) was varied between 1 and 20 mol% of the styrene units. Polyphase materials containing

  1. Blending of styrene-block-butadiene-block-styrene copolymer with sulfonated vinyl aromatic polymers

    NARCIS (Netherlands)

    Ruggeri, Giacomo; Passaglia, Elisa; Giorgi, Ivan; Picchioni, Francesco; Aglietto, Mauro

    2001-01-01

    Different polymers containing sulfonic groups attached to the phenyl rings were prepared by sulfonation of polystyrene (PS) and styrene-block-(ethylene-co-1-butene)-block-styrene (SEBS). The sulfonation degree (SD) was varied between 1 and 20 mol% of the styrene units. Polyphase materials containing

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

    OpenAIRE

    A.B. Moustafa; Rania Mounir; A.A. El Miligy; Maysa A. Mohamed

    2016-01-01

    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 u...

  3. MORPHOLOGY,INTERFACIAL INTERACTION AND PROPERTIES OF STYRENE-BUTADIENE RUBBER/MODIFIED HALLOYSITE NANOTUBE NANOCOMPOSITES

    Institute of Scientific and Technical Information of China (English)

    贾德民

    2009-01-01

    A natural nanotubular material,halloysite nanotubes(HNTs),was introduced to prepare styrene-butadiene rubber/modified halloysite nanotube(SBR/m-HNT) nanocomposites.Complex of resorcinol and hexamethylenetetramine (RH) was used as the interfacial modifier.The structure,morphology and mechanical properties of SBR/m-HNT nanocomposites,especially the interfacial interactions,were investigated.SEM and TEM observations showed that RH can not only facilitate the dispersion and orientation of HNTs in SBR matrix ...

  4. Modeling of continuous free-radical butadiene-styrene copolymerization process by the Monte Carlo method

    Directory of Open Access Journals (Sweden)

    T. A. Mikhailova

    2016-01-01

    Full Text Available In the paper the algorithm of modeling of continuous low-temperature free-radical butadiene-styrene copolymerization process in emulsion based on the Monte-Carlo method is offered. This process is the cornerstone of industrial production butadienestyrene synthetic rubber which is the most widespread large-capacity rubber of general purpose. Imitation of growth of each macromolecule of the formed copolymer and tracking of the processes happening to it is the basis of algorithm of modeling. Modeling is carried out taking into account residence-time distribution of particles in system that gives the chance to research the process proceeding in the battery of consistently connected polymerization reactors. At the same time each polymerization reactor represents the continuous stirred tank reactor. Since the process is continuous, it is considered continuous addition of portions to the reaction mixture in the first reactor of battery. The constructed model allows to research molecular-weight and viscous characteristics of the formed copolymerization product, to predict the mass content of butadiene and styrene in copolymer, to carry out calculation of molecular-weight distribution of the received product at any moment of conducting process. According to the results of computational experiments analyzed the influence of mode of the process of the regulator introduced during the maintaining on change of characteristics of the formed butadiene-styrene copolymer. As the considered process takes place with participation of monomers of two types, besides listed the model allows to research compositional heterogeneity of the received product that is to carry out calculation of composite distribution and distribution of macromolecules for the size and structure. On the basis of the proposed algorithm created the software tool that allows you to keep track of changes in the characteristics of the resulting product in the dynamics.

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

    OpenAIRE

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

    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 t...

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

    OpenAIRE

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

    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...

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

    Science.gov (United States)

    Adão; Saramago; Fernandes

    1999-09-01

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

  8. 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)

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

    Directory of Open Access Journals (Sweden)

    Khalil Ahmed

    2015-11-01

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

  10. 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.

  11. 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.

  12. 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.

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

    Institute of Scientific and Technical Information of China (English)

    魏东亚; 何宁; 王兆波

    2015-01-01

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

  14. Investigation on the mechanisms of genotoxicity of butadiene, styrene and their combination in human lymphocytes using the Comet assay.

    Science.gov (United States)

    Cemeli, Eduardo; Mirkova, Ekaterina; Chiuchiarelli, Giorgia; Alexandrova, Elena; Anderson, Diana

    2009-05-12

    The toxicity of butadiene and styrene is exerted by their metabolites. Such metabolites have been extensively scrutinized at the in vitro level demonstrating evident genotoxic properties. In monitoring, a diverse range of outcomes has been produced. Additionally, epidemiological studies in rubber workers face difficulties of data interpretation due to the changeability and multiple exposures of the workers as well as to confounding factors inherent to the cohorts. Nevertheless, toxicity has been associated with a significant trend of increasing the risk of leukaemia in employees at the styrene-butadiene rubber industry. Thus, further effort must be made to distinguish the exposures to each chemical over time and to characterize their interrelationships. The present investigation focuses on the effects and mechanisms of damage of the mixture styrene-butadiene by examining its metabolites: styrene oxide (SO), butadiene monoepoxide (BME) and butadiene diepoxide (BDE) respectively. The in vitro Comet assay on frozen lymphocytes has been employed to ascertain the DNA damage patterns for the styrene-butadiene metabolites combined and on their own. Different patterns were observed for the mixture and each of its components. This study has also led to determining the mechanism of damage of the mixture and the compounds. With regard to the presence of reactive oxygen species (ROS), co-treatment with catalase does not modulate the genotoxicity of the mixture but it does modulate its components. The outcomes also indicate that the mixture induces cross-links and this is due to the influence of BDE in the mixture, being more evident as the concentration of BDE increases. An investigation on the sensitivity of lymphocytes from occupationally un/exposed subjects to in vitro exposure of the mixture and its components revealed that occupationally exposed subjects had a substantially higher background of DNA damage and a lower sensitivity to the metabolites of styrene, 1

  15. Review of the toxicology of styrene.

    Science.gov (United States)

    Bond, J A

    1989-01-01

    Styrene is used in the production of plastics and resins, which include polystyrene resins, acrylonitrile-butadiene-styrene resins, styrene-acrylonitrile resins, styrene-butadiene copolymer resins, styrene-butadiene rubber, and unsaturated polyester resins. In 1985, styrene ranked in the top ten of synthetic organic chemicals produced in the U.S. This review focuses on various aspects of styrene toxicology including acute and chronic toxicity, carcinogenicity, genotoxicity, pharmacokinetics, effects on hepatic and extrahepatic xenobiotic-metabolizing enzymes, pharmacokinetic modeling, and covalent interactions with macromolecules. There appear to be many similarities between the toxicity and metabolism of styrene in rodents and humans. Needed areas of future research on styrene include studies on the molecular dosimetry of styrene in terms of both hemoglobin and DNA adducts. The results of such research should improve our ability to assess the relationship between exposure to styrene and surrogate measures of "effective dose", thereby improving our ability to estimate the effects of low-level human exposures.

  16. Perinatal Toxicity and Carcinogenicity Studies of StyreneAcrylonitrile Trimer, A Ground Water Contaminant

    Science.gov (United States)

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

    2015-01-01

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

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

    Science.gov (United States)

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

    2013-12-06

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

  18. Effect of crosslink density on some properties of electron beam-irradiated styrene-butadiene rubber

    Energy Technology Data Exchange (ETDEWEB)

    Wang Qingguo [Key Laboratory of Rubber-plastics of Ministry of Education, Qingdao University of Science and Technology, Qingdao 266042 (China); School of Polymer Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China)], E-mail: qwang@qust.edu.cn; Wang Fenlan [School of Polymer Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China); Cheng Kuo [Jiangsu Dasheng Heat Shrinkable Material Co., Ltd. Wujiang city 215214 (China)

    2009-11-15

    Crosslink densities of electron beam (EB)-irradiated styrene-butadiene rubber (SBR) samples were measured by using a novel magnetic resonance crosslink density spectrometer (MRCDS). With 1,1,1-trimethylolpropane triacrylate (TMPTA) loading increasing, the crosslink density of EB-irradiated SBR increases up to a certain level, and then decreases in the irradiation dose range 50-200 kGy. Tensile strength, elongation at break, thermal stability and pyrolysis products of the EB-irradiated SBR samples with different crosslink densities were also studied in this paper.

  19. Effect of crosslink density on some properties of electron beam-irradiated styrene-butadiene rubber

    Science.gov (United States)

    Wang, Qingguo; Wang, Fenlan; Cheng, Kuo

    2009-11-01

    Crosslink densities of electron beam (EB)-irradiated styrene-butadiene rubber (SBR) samples were measured by using a novel magnetic resonance crosslink density spectrometer (MRCDS). With 1,1,1-trimethylolpropane triacrylate (TMPTA) loading increasing, the crosslink density of EB-irradiated SBR increases up to a certain level, and then decreases in the irradiation dose range 50-200 kGy. Tensile strength, elongation at break, thermal stability and pyrolysis products of the EB-irradiated SBR samples with different crosslink densities were also studied in this paper.

  20. 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.

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

    Science.gov (United States)

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

    2012-04-01

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

  2. Effect of styrene-butadiene-styrene content on the adhesion properties of bitumen before and after heat aging

    Energy Technology Data Exchange (ETDEWEB)

    Zielinski, K. [Poznan Univ. of Technology, Poznan (Poland). Inst. of Structural Engineering

    2008-05-15

    Styrene-butadiene-styrene (SBS) is a common modifying polymer used in bitumen-based waterproofing building materials. SBS is used to improve the heat aging resistance of bitumen as well as to increase its resistance to temperature changes. This paper compared SBS-modified bitumen products with nonmodified bitumen products. The aim of the study was to assess the effect of heat aging and SBS content on the adhesion properties of 2 bitumen types to concrete and steel substrates. Two types of bitumen were tested: (1) paving-grade bitumen; and (2) an oxidized bitumen with a softening point at 25 degrees C. The thin film oven test was used to heat age the samples. Adhesion properties were measured before and after heat aging. The tests demonstrated that the adhesion strength of bituminous mastics to concrete and steel substrates decreased as SBS content increased. Bitumen products modified with 9 to 12 per cent of SBS showed a weaker bond with concrete and steel substrates than nonmodified equivalents. It was concluded that after heat aging, the adhesion strength of the nonmodified bitumen was higher than that of the bitumen modified with SBS. 7 refs., 4 tabs., 5 figs.

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

    Directory of Open Access Journals (Sweden)

    Er. Kapil Soni

    2014-03-01

    Full Text Available 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 the effects of polymer addition on compressive and flexural strength using concrete with mix design of constant water-cement ratio at local ambient temperature. The mixes were prepared with Styrene-Butadiene Rubber (SBR latex -cement ratio of 0 %, 5%, 10%, 15% and 20%. Slump test was conducted on fresh concrete while compressive strength and flexural strength were determined at different age. A locally available Perma-Latex is used as SBR Latex. It has been observed that SBR latex has negative effect at early age while at 28 days, the addition of SBR latex in concrete results in enhancement of compressive strength and Flexural Strength. Based on the results of this study, latex modified concrete made using Perma-Latex may be recommended to be used with various types of concrete structures. However, for the mixes rich in cement, the dosage of SBR latex needs to be adjusted to maintain required workability of concrete.

  4. 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

    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.%).......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 addition...... of the Psingle bondH containing fire retardants to a double bonds of poly(butadiene) block of SBS were found, affording varied degree of the modification (0.2–21 mol%). Alternatively, a two-step procedure based on an epoxidation step followed by hydrolysis of the epoxides with phosphoric acid was developed...

  5. 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 addition...... resulting in 20 mol% of poly(butadiene) block modification. Based on TGA results, organophosporus-modified SBS was found to be amenable to charring – a property which correlated directly with the reduced flammability of the modified polymer observed in Cone Calorimetry tests. Furthermore, conceptually novel...... 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.%)....

  6. 40 CFR 63.500 - Back-end process provisions-carbon disulfide limitations for styrene butadiene rubber by emulsion...

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 9 2010-07-01 2010-07-01 false Back-end process provisions-carbon disulfide limitations for styrene butadiene rubber by emulsion processes. 63.500 Section 63.500 Protection... Pollutant Emissions: Group I Polymers and Resins § 63.500 Back-end process provisions—carbon disulfide...

  7. 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...

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

    Science.gov (United States)

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

    2013-12-01

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

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

    Indian Academy of Sciences (India)

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

    2016-02-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-09-15

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

  11. 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.

  12. Radiation crosslinking of styrene-butadiene rubber containing waste tire rubber and polyfunctional monomers

    Science.gov (United States)

    Yasin, Tariq; Khan, Sara; Shafiq, Muhammad; Gill, Rohama

    2015-01-01

    The objective of this study was to investigate the influence of polyfunctional monomers (PFMs) and absorbed dose on the final characteristics of styrene-butadiene rubber (SBR) mixed with waste tire rubber (WTR). A series of SBR/WTR blends were prepared by varying the ratios of WTR in the presence of PFMs, namely trimethylolpropane trimethacrylate (TMPTMA) and trimethylolpropane triacrylate (TMPTA) and crosslinked using gamma rays. The physicochemical characteristics of the prepared blends were investigated. It was observed that tensile strength, hardness and gel content of the blends increased with absorbed dose while the blends containing TMPTA showed higher tensile strength, gel content and thermal stability as compared to the blends containing TMPTMA. Higher thermal stability was observed in the blends which were crosslinked by radiation as compared to the blends crosslinked by sulfur. These blends exhibited higher rate of swelling in organic solvents, whereas negligible swelling was observed in acidic and basic environment.

  13. Synthesis and characterization of miktoarm star copolymer of styrene and butadiene using multifunctional macromolecular initiator

    Institute of Scientific and Technical Information of China (English)

    Hai Yan Zhang; Xing Ying Zhang

    2009-01-01

    A new kind of multifunctional macromolecular initiator with Sn-C bonds and polydiene arms was synthesized by living anionic polymerization.At first,polydiene-stannum chloride(PD-SnCl3)was prepared by the reaction of n-butyl-Li(n-BuLi),stannic chloride(SnCl4)and diene.Then PD-SnCl3 was used to react with the dilithium initiator to prepare the multifunctional organic macromolecular initiators.The result suggested that the initiators had a remarkable yield by GPC,nearly 90%.By using these multifunctional macromolecular initiators,styrene and butadiene were effectively polymerized via anionic polymerization,which gave birth to novel miktoarm star copolymers.The relative molecular weight and polydispersity index,microstructure contents,copolymerization components,glass transition temperature(Tg)and morphology of the miktoarm star copolymers were investigated by GPC-UV,1H NMR,DSC and TEM,respectively.

  14. Experimental thermal transport evolution of silane activated nano-clay reinforced styrene butadiene elastomeric nanocomposites

    Science.gov (United States)

    Iqbal, S. S.; Iqbal, N.; Jamil, T.; Bashir, A.; Shahid, M.

    2016-08-01

    In this study, silane activated nanoclay was reinforced in styrene butadiene rubber (SBR) to enhance the thermal resistance/stability and mechanical properties of SBR. silane activated nanoclay with variant concentrations was impregnated in the rubber matrix to fabricate polymer nanocomposites under control processing conditions. Experimental thermal transport, thermal oxidation, phase transition study, and mechanical properties of the nanocomposite specimens were carried out. Thermal insulation, thermal stability, and heat flow response were remarkably enhanced with the addition of nanokaolinite in the polymer matrix. Phase transition temperatures, their corresponding enthalpies, tensile strength, elastic modulus, elongation at break and hardness of the rubber composites were positively influenced with the filler incorporation into the host matrix. The Even dispersion of nanoreinforcements, morphological and compositional analyses of the thermal transport tested specimens were performed using scanning electron microscopy and energy dispersive spectroscopy, respectively.

  15. 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.

  16. 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)

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

    Science.gov (United States)

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

    2012-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

    刘健; 程斌

    2011-01-01

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

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

    Directory of Open Access Journals (Sweden)

    S. Benali

    2008-01-01

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

  20. 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.

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

    Science.gov (United States)

    Mansilla, M. A.; Marzocca, A. J.

    2012-08-01

    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.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. MORPHOLOGY, INTERFACIAL INTERACTION AND PROPERTIES OF STYRENE-BUTADIENE RUBBER/MODIFIED HALLOYSITE NANOTUBE NANOCOMPOSITES

    Institute of Scientific and Technical Information of China (English)

    Zhi-xin Jia; Yuan-fang Luo; Shu-yan Yang; Bao-chun Guo; Ming-liang Du; De-min Jia

    2009-01-01

    A natural nanotubular material, halloysite nanotubes (HNTs), was introduced to prepare styrene-butadiene rubber/modified halloysite nanotube (SBR/m-HNT) nanocomposites. Complex of resorcinol and hexamethylenetetramine (RH) was used as the interracial modifier. The structure, morphology and mechanical properties of SBR/m-HNT nanocomposites, especially the interfacial interactions, were investigated. SEM and TEM observations showed that RH can not only facilitate the dispersion and orientation of HNTs in SBR matrix at nanometer scale, but also enhance the interracial combination between HNTs and rubber matrix. FTIR and XPS investigations confirmed that a number of hydrogen bonds were formed between the phenol hydroxyl groups in resorcinol-formaldehyde resin derived from RH and the oxygen atoms in Si-O bonds or hydroxyl groups on HNTs surfaces. The m-HNTs modified with RH have significant reinforcing effect on SBR vulcanizates. RH as a good interfacial modifier can remarkably improve mechanical properties of SBR/HNT composites. The substantial improvement of comprehensive properties for SBR/m-HNT nanocomposites can be attributed to good dispersion and orientation of HNTs in SBR matrix at nanometer scale and the enhanced interracial interaction between HNTs and rubber matrix.

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

    NARCIS (Netherlands)

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

    1994-01-01

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

  9. 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.

  10. 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.

  11. 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.

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

    Science.gov (United States)

    2014-12-01

    explores the fused deposition modeling ( FDM ) and the printing orientation as a means to quantify the potential benefits. These benefits include more cost...effective, time-efficient, in-house fabrication of designs, while optimizing the mechanical and structural integrity. In FDM , CAD software is used to...relationship to the stress experienced in a material at high-strain-rate deformation. For polymers such as ABS, the mechanical properties vary

  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. 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.

  15. Radiation-induced copolymerization of styrene/ n-butyl acrylate in the presence of ultra-fine powdered styrene-butadiene rubber

    Science.gov (United States)

    Yu, Haibo; Peng, Jing; Zhai, Maolin; Li, Jiuqiang; Wei, Genshuan; Qiao, Jinliang

    2007-11-01

    Styrene (St)/ n-butyl acrylate (BA) copolymers were prepared by two-stage polymerization: St/BA was pre-polymerized to a viscous state by bulk polymerization with initiation by benzoyl peroxide (BPO) followed by 60Co γ-ray radiation curing. The resultant copolymers had higher molecular weight and narrower molecular weight distribution than conventional methods. After incorporation of ultra-fine powdered styrene-butadiene rubber (UFSBR) with a particle size of 100 nm in the monomer, the glass transition temperature ( Tg) of St-BA copolymer increased at low rubber content. Both the St-BA copolymer and the St-BA copolymer/UFSBR composites had good transparency at BA content below 40%.

  16. Variation of long periodicity in blends of styrene butadiene, styrene copolymer/polyaniline using small angle X-ray scattering data

    Indian Academy of Sciences (India)

    B G Soares; Fernando G Souza Jr; A Manjunath; H Somashekarappa; R Somashekar; Siddaramaiah

    2007-09-01

    Small angle X-ray scattering data have been recorded for the blends of styrene butadiene, styrene copolymer/polyaniline using the beamline of the LNLS (Laboratorio Nacional de Luz sincroton-Campinas, Brazil). Employing one-dimensional Hosemann's paracrystalline model, we have simulated the meridional reflections of these blends in order to compute the long periodicity and hence to find the variation with concentrations of the blends. Within the region of available experimental data we observe that there is a linear relationship between long periodicity and concentration of blends. These parameters are compared with physical measurements like tensile strength to find the structure–property relation in these blends.

  17. -Styrene)

    KAUST Repository

    Sutisna, Burhannudin

    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.

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

    Institute of Scientific and Technical Information of China (English)

    李再峰; 董慧民; 刘晓丹; 李敏婷; 张成龙; 熊召举

    2011-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

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

    2003-01-01

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

  20. Temperature dependence on free volume in cured natural rubber and styrene-butadiene rubber blends

    Science.gov (United States)

    Salgueiro, W.; Somoza, A.; Silva, L.; Consolati, G.; Quasso, F.; Mansilla, M. A.; Marzocca, A. J.

    2011-05-01

    A systematic study on the evolution of free volume as a function of the temperature in vulcanized at 433 K natural rubber (NR) and styrene butadiene rubber (SBR) in 25-75, 50-50, 75-25 NR-SBR (percent content of pure NR and SBR, respectively) blends was studied by positron annihilation lifetime spectroscopy. All samples were prepared with sulfur and TBBS (n-t-butyl-2-benzothiazole sulfenamide) as accelerator. The glass transition temperatures of the samples studied were determined by differential scanning calorimetry (DSC) and from lifetime data. In general, a sigmoidal-like complex behavior of the long-lived lifetime component, linked to the nanohole free volume, as a function of the temperature was found. For SBR, the slope of the ortho-positronium lifetime against temperature curves could be well-fitted using a linear function. For blends and also for NR, two different linear functions were necessary. This last behavior is explained in terms of the supercooled process involving a reconfiguration of the elastomeric chains. In the case of blends, the state of cure of NR and SBR in each NR-SBR sample was also taken into account in the discussion of the results obtained. Besides, thermal expansion coefficients of the free volumes in the transition and glassy region of all compounds were estimated. The differences observed in the values of this parameter are discussed by taking into account the morphology and formulation of each blend, the crosslink densities, and the role of the interphases formed between both NR and SBR elastomers.

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

    Science.gov (United States)

    Marwat, Zafrullah Khan; Baloch, Musa Kaleem

    2016-11-01

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

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

    Science.gov (United States)

    Osterman-Golkar, S; Bond, J A

    1996-10-01

    The 1990 Clean Air Act Amendments list several volatile organic chemicals as hazardous air pollutants, including ethylene oxide, butadiene, styrene, and acrylonitrile. The toxicology of many of these compounds shares several common elements such as carcinogenicity in laboratory animals, genotoxicity of the epoxide intermediates, involvement of cytochrome P450 for metabolic activation (except ethylene oxide), and involvement of at least two enzymes for detoxication of the epoxides (e.g., hydrolysis or conjugation with glutathione). These similarities facilitate research strategies for identifying and developing biomarkers of exposure. This article reviews the current knowledge about biomarkers of butadiene. Butadiene is carcinogenic in mice and rats, which raises concern for potential carcinogenicity in humans. Butadiene is metabolized to DNA-reactive metabolites, including 1,2-epoxy-3-butene and diepoxybutane. These epoxides are thought to play a critical role in butadiene carcinogenicity. Butadiene and some of its metabolites (e.g., epoxybutene) are volatile. Exhalation of unchanged butadiene and excretion of butadiene metabolites in urine represent major routes of elimination. Therefore, biomonitoring of butadiene exposure could be based on chemical analysis of butadiene in exhaled breath, blood levels of butadiene epoxides, excretion of butadiene metabolites in urine, or adducts of butadiene epoxides with DNA or blood proteins. Mutation induction in specific genes (e.g., HPRT) following butadiene exposure can be potentially used as a biomarker. Excretion of 1,2-dihydroxy-4-(N-acetylcysteinyl-S)butane or the product of epoxybutene with N-7 in guanine in urine, epoxybutene-hemoglobin adducts, and HPRT mutation have been used as biomarkers in recent studies of occupational exposure to butadiene. Data in laboratory animals suggest that diepoxybutane may be a more important genotoxic metabolite than epoxybutene. Biomonitoring methods need to be developed for

  3. 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

  4. 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 ...

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

    OpenAIRE

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

    1996-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

    桂强; 梁琨; 钟启林; 马朋高; 张元寿; 王真琴

    2011-01-01

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

  7. 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.

  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. 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.

  10. Innovative neutron shielding materials composed of natural rubber-styrene butadiene rubber blends, boron oxide and iron(III) oxide

    Science.gov (United States)

    Jumpee, C.; Wongsawaeng, D.

    2015-05-01

    Optimized flexible and lightweight neutron shielding materials were designed using the Monte Carlo N-Particle (MCNP) code. Thicknesses of 10 mm and 100 mm were tested for neutron shielding performances. Simulation results indicated that the 10 mm shielding material of natural rubber (NR) and styrene butadiene rubber (SBR) blend (1:1) with 60 part per hundred rubber (phr) boron oxide (B2O3) and 100 mm shielding material with four alternating layers of NR with 100 phr iron (III) oxide (Fe2O3) and of NR and SBR blend (1:1) with 10 phr B2O3 were most suitable for thermal neutron shielding and all-energy neutron shielding, respectively. Experimental results verified the shielding efficiency of these optimal designs and ease of fabrication.

  11. 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.

  12. 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 butadienestyrene 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.

  13. 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...

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

    Indian Academy of Sciences (India)

    Garima Tripathi; Deepak Srivastava

    2009-04-01

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

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

    Science.gov (United States)

    Li, Daishuang; Xia, Haibing; Peng, Jing; Zhai, Maolin; Wei, Genshuan; Li, Jiuqiang; Qiao, Jinliang

    2007-11-01

    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.

  16. 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.

  17. 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.

  18. Mortality of a cohort of workers in the styrene-butadiene polymer manufacturing industry (1943-1982)

    Energy Technology Data Exchange (ETDEWEB)

    Matanoski, G.M.; Santos-Burgoa, C.; Schwartz, L. (Johns Hopkins School of Hygiene and Public Health, Baltimore, MD (USA))

    1990-06-01

    A cohort of 12,110 male workers employed 1 or more years in eight styrene-butadiene polymer (SBR) manufacturing plants in the United States and Canada has been followed for mortality over a 40-year period, 1943 to 1982. The all-cause mortality of these workers was low (standardized mortality ratio (SMR) = 0.81) compared to that of the general population. However, some specific sites of cancers had SMRs that exceeded 1.00. These sites were then examined by major work divisions. The sites of interest included leukemia and non-Hodgkin's lymphoma in whites. The SMRs for cancers of the digestive tract were higher than expected, especially esophageal cancer in whites and stomach cancer in blacks. The SMR for arteriosclerotic heart disease in black workers was significantly higher than would be expected based on general population rates. Employees were assigned to a work area based on job longest held. The SMRs for specific diseases differed by work area. Production workers showed increased SMRs for hematologic neoplasms and maintenance workers, for digestive cancers. A significant excess SMR for arteriosclerotic heart disease occurred only in black maintenance workers, although excess mortality from this disease occurred in blacks regardless of where they worked the longest. A significant excess SMR for rheumatic heart disease was associated with work in the combined, all-other work areas. For many causes of death, there were significant deficits in the SMRs.

  19. Mortality of a cohort of workers in the styrene-butadiene polymer manufacturing industry (1943-1982).

    Science.gov (United States)

    Matanoski, G M; Santos-Burgoa, C; Schwartz, L

    1990-01-01

    A cohort of 12,110 male workers employed 1 or more years in eight styrene-butadiene polymer (SBR) manufacturing plants in the United States and Canada has been followed for mortality over a 40-year period, 1943 to 1982. The all-cause mortality of these workers was low [standardized mortality ratio (SMR) = 0.81] compared to that of the general population. However, some specific sites of cancers had SMRs that exceeded 1.00. These sites were then examined by major work divisions. The sites of interest included leukemia and non-Hodgkin's lymphoma in whites. The SMRs for cancers of the digestive tract were higher than expected, especially esophageal cancer in whites and stomach cancer in blacks. The SMR for arteriosclerotic heart disease in black workers was significantly higher than would be expected based on general population rates. Employees were assigned to a work area based on job longest held. The SMRs for specific diseases differed by work area. Production workers showed increased SMRs for hematologic neoplasms and maintenance workers, for digestive cancers. A significant excess SMR for arteriosclerotic heart disease occurred only in black maintenance workers, although excess mortality from this disease occurred in blacks regardless of where they worked the longest. A significant excess SMR for rheumatic heart disease was associated with work in the combined, all-other work areas. For many causes of death, there were significant deficits in the SMRs. PMID:2401250

  20. 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.

  1. 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.

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

    Institute of Scientific and Technical Information of China (English)

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

    2012-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

    Osterman-Golkar, S. [Stockholm Univ. (Sweden); Bond, J.A. [Chemical Industry Institute of Toxicology, Research Triangle Park, NC (United States)

    1996-10-01

    The 1990 Clean Air Act Amendments list several volatile organic chemicals as hazardous air pollutants, including ethylene oxide, butadiene, styrene, and acrylonitrile. The toxicology of many of these compounds shares several common elements such as carcinogenicity in laboratory animals, genotoxicity of the epoxide intermediates, involvement of cytochrome P450 for metabolic activation (except ethylene oxide), and involvement of at least two enzymes for detoxication of the epoxides (e.g., hydrolysis or conjugation with glutathione). These similarities facilitate research strategies for identifying and developing biomarkers of exposure. This article reviews the current knowledge about biomarkers of butadiene. Butadiene is carcinogenic in mice and rats, which raises concern for potential carcinogenicity in humans. 85 refs., 1 fig., 2 tabs.

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

    Institute of Scientific and Technical Information of China (English)

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

    2009-01-01

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

  5. STUDY ON THE SEQUENCE STRUCTURE OF BUTADIENE-STYRENE RUBBER BY 13C-NMR METHOD Ⅲ. QUANTITATIVE CHARACTERIZATION OF SEQUENCE STRUCTURE

    Institute of Scientific and Technical Information of China (English)

    CHEN Xiaonong; HU Liping; YAN Baozhen; JIAO Shuke

    1990-01-01

    The quantitative description of the sequence structure of emulsion-processed SBR and solution-processed SBR (by lithium catalyst)was carried out based on their spectral data of 13C-NMR.The calculating formulae which could be used to obtain diad concentration from the peak intensities of carbon spectra, average block length, average number of block, and the microstructure composition of the molecular chain were derived. The quantitative result showed that on the molecular chain styrene unit had the tendency to attach to trans-1,4 butadiene unit. The calculated result of the microstructure was in good agreement with that obtained through IR measurement.

  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.

  7. 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.

  8. 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.

  9. 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.

  10. Poly(styrene-co-butadiene) random copolymer thin films and nanostructures on a mica surface: morphology and contact angles of nanodroplets.

    Science.gov (United States)

    McClements, Jake; Buffone, Cosimo; Shaver, Michael P; Sefiane, Khellil; Koutsos, Vasileios

    2017-09-20

    The self-assembly of poly(styrene-co-butadiene) random copolymers on mica surfaces was studied by varying solution concentrations and polymer molecular weights. Toluene solutions of the poly(styrene-co-butadiene) samples were spin coated onto a mica surface and the resulting polymer morphology was investigated by atomic force microscopy. At higher concentrations, thin films formed with varying thicknesses; some dewetting was observed which depended on the molecular weight. Total dewetting did not occur despite the polymer's low glass transition temperature. Instead, partial dewetting was observed suggesting that the polymer was in a metastable equilibrium state. At lower concentrations, spherical cap shaped nanodroplets formed with varying sizes from single polymer chains to aggregates containing millions of chains. As the molecular weight was increased, fewer aggregates were observed on the surface, albeit with larger sizes resulting from increased solution viscosities and more chain entanglements at higher molecular weights. The contact angles of the nanodroplets were shown to be size dependent. A minimum contact angle occurs for droplets with radii of 100-250 nm at each molecular weight. Droplets smaller than 100 nm showed a sharp increase in contact angle; attributed to an increase in the elastic modulus of the droplets, in addition, to a positive line tension value. Droplets larger than 250 nm also showed an increased contact angle due to surface heterogeneities which cannot be avoided for larger droplets. This increase in contact angle plateaus as the droplet size reaches the macroscopic scale.

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

    Institute of Scientific and Technical Information of China (English)

    王真琴; 吴福生; 梁滔; 龚光碧

    2012-01-01

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

  12. Investigation of mechanisms of polycyclic aromatic hydrocarbons (PAHs) initiated from the thermal degradation of styrene butadiene rubber (SBR) in N2 atmosphere.

    Science.gov (United States)

    Kwon, Eilhann; Castaldi, Marco J

    2008-03-15

    This study has been carried out to characterize the thermal decomposition of styrene-butadiene rubber (SBR), using thermogravimetric analysis (TGA) coupled to online GC/MS, and to investigate the formation and ultimate fate of chemical species produced during gasification of SBR. A preliminary mechanistic understanding has been developed to explain the formation and relationship of light hydrocarbons (C1-C4), substituted aromatics, and polycyclic aromatic hydrocarbons (PAHs) during the decomposition of SBR in a N2 atmosphere. Identification and absolute concentrations of over 50 major and minor species (from hydrogen to benzo[ghi]perylene) have been established, and the measurements have been carried out between 300 and 500 at 10 degrees C/min heating rate in a N2 atmosphere. The concentration of styrene reached 120 PPMV and the concentration of other substituted aromatics, such as toluene and ethyl benzene reached 20 and 5 PPMV, respectively. These measurements indicate PAH formation at a relatively lower temperature as compared to conventional fuel, such as coal and diesel. The PAH sequence is not simply the constructing of larger PAHs from smaller ones to achieve the complex polymer structures. It is possible to generate large PAH molecules while circumventing the typical construction pathway.

  13. SBS辐射交联对SBS/PA6共混物性能的影响%Improving compatibility of styrene-butadiene-styrene/polyamide 6 blends by radiation crosslinking of the SBS

    Institute of Scientific and Technical Information of China (English)

    张艳; 谢雷东; 盛康龙

    2009-01-01

    本文为提高苯乙烯-丁二烯-苯乙烯嵌段共聚物(Styrene-Butadiene-Styrene triblock copolymer,SBS)与尼龙6(PA6)共混物的相容性,利用SBS的辐射交联对其进行辐射改性,赋予共混物更好的性能.SBS在常温空气气氛下~(60)Co γ射线辐照至一定剂量发生化学交联,在共混物内形成三维网络结构,使两相间产生强制互容作用.对改性前后共混物微观形貌,流变性能,机械性能及吸水性的分析与表征.结果表明,辐射交联改性增容后SBS/PA6聚合物合金的性能得到明显提高.

  14. 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)

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2008-11-25

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

  16. 纤维素纳米纤维-丁苯胶乳复合材料的制备与表征%Preparation and characterization of cellulose-nanoifbers/styrene-butadiene latex (NFs/SBL) composites

    Institute of Scientific and Technical Information of China (English)

    宋冰; 石勇; 陆海龙; 马金霞; 周小凡

    2016-01-01

    采用共混法制备不同纤维素纳米纤维含量的纤维素纳米纤维-丁苯胶乳复合材料,并通过拉伸性能、扫描电镜、热重分析以及红外光谱检测该复合材料的相关性能。分析结果表明:纤维素纳米纤维能均匀分散在丁苯胶乳溶液中,对丁苯胶乳有较好的补强效果;和丁苯胶乳相比,制得复合材料的裂断伸长率增大,弹性变好;但纤维素纳米纤维的加入对丁苯胶乳热稳定性的影响不明显。%Cellulose-nanofibers/styrene-butadiene latex(NFs-SBL) composites were prepared by blending different amount of cellulose nanofibers with styrene-butadiene latex(SBL), through the tensile properties testing, scanning electron microscopy (SEM), thermo-gravimetric analysis and infrared spectrometric analysis(FT-IR). The result showed that NFs are dispersed uniformly in styrene-butadiene latex and showed a good reinforcing effect on SBL, composite material breaking elongation increased and elastic becoming good. However, the addition of NFs had a less impact on thermal stability of styrene-butadiene latex.

  17. Dynamic Mechanical Property of Styrene-Butadiene Rubber/Natural Rubber Composite%丁苯橡胶/天然橡胶复合体系动态力学性能

    Institute of Scientific and Technical Information of China (English)

    徐文总; 郝文涛; 马德柱; 梁俐

    2001-01-01

    The dynamic mechanical properties of blends of natural rubberrespectively with three kinds of styrene-butadiene rubbers, two solution polymerized styrene-butadiene rubbers: SSBR(B), SSBR(C) and an emulsion polymerized styrene-butadiene rubber:ESSA have been investigated. The results showed that SSBR(B) had characteristic chain structure and the SSBR/NR composite showed a good compatibility and low heat generation under pressure.%选取乳聚丁苯橡胶、溶聚丁苯橡胶(C)和溶聚丁苯橡胶(B)3种典型的丁苯橡胶,研究了它们与天然橡胶复合体系的动态力学性能.结果表明,溶聚丁苯橡胶SSBR(B)具有特征的链化学结构,与天然橡胶有良好的混容性.溶聚丁苯橡胶/天然橡胶复合体系生热低,而且具有比较均匀的交联网状结构.

  18. Thermal oxidative and ozone oxidative stabilization effect of hybridized functional graphene oxide in a silica-filled solution styrene butadiene elastomer.

    Science.gov (United States)

    Su, Juqiao; Zhao, Zhongguo; Huang, Yajiang; Liao, Xia; Yang, Qi

    2016-10-26

    Hybridization of modified functional graphene oxide (fGO) in silica-filled solution styrene butadiene rubber (SSBR) endows preferable tensile and dynamic properties before and after thermal oxidative aging, and similar mechanical hysteresis performance compared with the composites without fGO. The preventing mechanism of fGO is attributed to its intrinsic peroxy radical scavenging and gas barrier abilities, which significantly reduces the peroxy radical concentration and oxygen permeability of nanocomposites and then prolongs oxidative induction time (OIT), characterized by differential scanning calorimetry (DSC). The ozone resisting effect of different loadings of fGO on nanocomposites have also been investigated by Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM) after ozonization under 50 ppm ozone concentration. As a result, incorporation of fGO apparently suppresses both the formation of oxygenic groups of the olefinic elastomer and crack morphology extension upon ozonization. We propose that fGO protects the SSBR elastomer from ozone attack through the conjugated delocalized π-bonds of the fGO instead of the C[double bond, length as m-dash]C bonds of the elastomer matrix being attacked, and the compared experiments, characterized by X-ray photoelectron spectroscopy (XPS), confirm that this presumption is perhaps reasonable. Moreover, more than 3 phr incorporation of fGO in nanocomposites deteriorates the chemical and mechanical properties of the elastomer during the thermal oxidation and ozonization because of the cleavage influence of oxygenic groups on peroxy radicals.

  19. 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.

  20. 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.

  1. 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.

  2. Fabrication of conducting composite sheets using cost-effective graphite flakes and amorphous styrene acrylonitrile for enhanced thermistor, dielectric, and electromagnetic interference shielding properties

    Energy Technology Data Exchange (ETDEWEB)

    Panwar, Varij, E-mail: varijpanwarcertain@gmail.com [Electronics and Communication Engineering, Graphic Era University, Dehradun, Uttarakhand (India); Gill, Fateh Singh; Rathi, Vikas; Tewari, V.K. [Electronics and Communication Engineering, Graphic Era University, Dehradun, Uttarakhand (India); Mehra, R.M. [Sharda University, Greater Noida (India); Park, Jong-Oh, E-mail: jop@jnu.ac.kr [School of Mechanical Engineering, Chonnam National University, Gwangju (Korea, Republic of); Park, Sukho, E-mail: shpark12@dgist.ac.kr [Department of Robotics Engineering, Daegu Gyeongbuk Institute of Science and Technology, Daegu (Korea, Republic of)

    2017-06-01

    The fabrication of strong conducting composite sheets (CCSs) using a simple technique with cost-effective materials is desirable for capacitor, decoupling capacitor, and electromagnetic interference (EMI) shielding applications. Here, we used cost-effective graphite flakes (GFs) as a conducting filler and amorphous poly (styrene-co-acrylonitrile) (PSAN) as an insulating polymer to fabricate a CCS via a simple mechanical mixing and hot compression molding process in 2.5 h, with the aim to save time and avoid the use of toxic reagents, which are generally used in chemical methods. In the present method, the GFs are connected in diffusively adhere polymer matrix, controlled by temperature and pressure that generate the conduction in the CCSs. The resulting PSAN/GF CCSs were characterized by using scanning electron microscopy (SEM), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and hardness tests. The GFs penetrated the interfacial region of PSAN, thus improving the thermistor and dielectric properties (dielectric constant, AC conductivity, and dissipation factor) of the PSAN/GF CCSs. Furthermore, the PSAN/GF CCSs showed enhanced hardness and EMI shielding effectiveness (SE) properties in the X-band frequency range (8.5–12.5 GHz). The percolation theory was implemented to DC and AC conductivity. To detect the transition of the dielectric properties, the dielectric constant of the CCSs was analyzed with increasing volume fraction of GFs in the radio frequency region. The improved dielectric constant, AC conductivity, and dissipation factor of the PSAN/GF CCS, indicated a significant improvement in their EMI shielding properties in the X-band frequency range, which were measured using the waveguide method. The ac conductivity of PSAN/GF CCS shows stable behavior in the higher frequency ranges. The EMISE of PSAN/GF CCS were found to increase with increasing GF content due to the absorbance mechanism. - Highlights: • Enhanced hardness and

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

    Institute of Scientific and Technical Information of China (English)

    尹国强; 李杨; 申凯华; 张峰; 张东梅; 史晶虹; 王玉荣

    2013-01-01

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

  4. Application of solution polymerized styrene-butadiene rubber 2557-A in tire%溶聚丁苯橡胶2557-A在轮胎中的应用

    Institute of Scientific and Technical Information of China (English)

    徐燕; 孙举涛; 徐文清; 张萍; 孙学红

    2012-01-01

    In accordance with the pure carbon black formula, solution polymerized styrene-butadiene rubber ( SSBR, grade 2557-A) and emulsion styrene-butadiene rubber(ESBR, grade 1712) were applied to crown rubbers of all-steel and semi-steel radial tires seperately, their application results were compared, and the acceptable crown rubber formula of SSBR 2557-A was achieved. The all-steel and semi-steel radial tires were trial-produced, and their performances were tested. The results showed that compared to ESBR 1712 all-ateel crown vulcanizate. The tensile strength, modulus at 100% and 300% , abrasion resistance ( Akron) , compression heat built-up as well as the balance between wet skid resistance and rolling resistance of the equivalent SSBR 2557-A crown vulcani- zate increased, but abrasion resistance ( DIN ) decreased- And compared to ESBR 1712 semi-stell crown vulcanizate, the equivalent SSBR 2557-A also improved semi-steel crown vulcanizate in skid resistance without changing any other performances. The trial tire based on SSBR 2557-A all-steel crown rubber formula passed endurance test, and the tire based on SSBR 2557-A semi-steel crown rubber formula met the national standard in outer dia, strength, unseating resistance, highspeed performance and durability, in addition, it had substantial high wet skid resistance and noise performance.%按照纯炭黑配方,将溶聚丁苯橡胶(SSBR,牌号为2557 -A)同乳聚丁苯橡胶(ESBR,牌号为1712)对比应用于全钢和半钢子午线轮胎胎冠胶配方中,确定了合适的胎冠胶配方,且进行了轮胎的试制和性能检测.结果表明,与ESBR 1712全钢胎冠胶相比,同等用量SSBR 2557 -A的胎冠胶拉伸强度、定伸应力、Akron磨耗性能和压缩生热等性能均得到提高,但DIN磨耗性能有所下降,且具有更优的抗湿滑性和更低的滚动阻力;与ESBR 1712半钢胎冠胶相比,SSBR 2557 -A胎冠胶具有优异的抗湿滑性能,而其他性能相差不大;采用SSBR 2557 -A

  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. Synthesis and characterization of poly(styrene-co-methyl methacrylate); Sintese e caracterizacao do poli(estireno-co-metacrilato de metila)

    Energy Technology Data Exchange (ETDEWEB)

    Augustinho, Tiago R.; Abarca, Silvia A.C.; Machado, Ricardo A.F. [Departamento de Engenharia Quimica e Alimentos - Universidade Federal de Santa Catarina - UFSC, Florianopolis, SC (Brazil)

    2011-07-01

    Polystyrene (PS) is nowadays commonly used due its advantages over competitors. PS presents a lower cost when compared with Acrylonitrile Butadiene Styrene (ABS) and with Polyethylene Tere-phthalate (PET), and can be easier processed than polypropylene (PP). At expandable form (EPS), can be used as projective equipment, thermal insulation, floating boards, refrigerators, isothermal, and low cost applications such as packaging and disposable material. Searching for more resistant materials and with a low cost, researches with copolymers materials are being developed. In this study, copolymerization reactions were carried out by suspension polymerization using monomers styrene and methyl methacrylate (MMA) with styrene. Styrene was in the highest percentage in relation to the MMA. The MMA was selected because is a monomer that presents a higher resistance than PS. The copolymerization was confirmed by performing infrared spectroscopy (IR), nuclear magnetic resonance of hydrogen (RMN{sup 1}H), differential scanning calorimetry (DSC) and thermogravimetry (TGA). (author)

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

    Institute of Scientific and Technical Information of China (English)

    高杜娟; 黄世英; 赵家琳; 刘俊保

    2015-01-01

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

  8. Effect of nano-scaled styrene butadiene rubber based nucleating agent on the thermal, crystallization and physical properties of isotactic polypropylene

    Energy Technology Data Exchange (ETDEWEB)

    Petchwattana, Nawadon [Division of Polymer Materials Technology, Faculty of Agricultural Product Innovation and Technology, Srinakharinwirot University, Sukhumvit 23, Wattana, Bangkok 10110 (Thailand); Covavisaruch, Sirijutaratana, E-mail: sirijutaratana.c@chula.ac.th [Department of Chemical Engineering, Faculty of Engineering, Chulalongkorn University, Pathumwan, Bangkok 10330 (Thailand); Sripanya, Panjapong [Thai Oleochemicals Company Limited (A Subsidiary of PTT Global Chemical Public Company Limited), Mueang Rayong, Rayong 21150 (Thailand)

    2014-01-05

    Highlights: • The effect of a SBR based β-NA on the properties iPP was investigated. • The addition of β-NA led to higher population of nuclei and smaller spherulites. • β to α phase transformation was observed when re-extrusion process was applied. • Impact strength was increased when the β-NA was added from 0.10 to 0.20 wt%. -- Abstract: The influence of a specific nano-scaled styrene butadiene rubber based β-nucleating agent (β-NA) on the properties of isotactic polypropylene (iPP) was investigated in the current research. β-NA was applied at the concentration ranged from 0.05 to 0.50 wt%. Microscopic observation revealed that the neat iPP crystals grew very slowly; they ranged in size from 100 to 200 μm. The addition of β-NA led to higher population of nuclei and smaller spherulites than those found in neat iPP. The addition of only 0.05 wt% β-NA significantly decreased the sizes of the spherulites down to 5 μm; the crystal grew very rapidly, leading to extremely fine morphology. Analysis by X-ray diffraction (XRD) confirmed that iPP/β-NA constituted mainly of β-crystal structure. The transformation of β to α phase was observed upon re-extrusion, it was verified by the lowered fraction of the β-crystalline phase (K{sub β}) although the total degree of crystallinity remained unchanged. A significant improvement in the impact strength of the iPP/β-NA was observed when the β-NA was employed from 0.10 to 0.20 wt%, leading to the formation of tough β-crystals in the β-NA nucleated iPP. The color measurement implied that the iPP nucleated with β-NA was superior in terms of whiteness but it was less transparent, as was evident by the increased haze.

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

    Institute of Scientific and Technical Information of China (English)

    王盎然; 包永忠; 翁志学; 黄志明

    2008-01-01

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

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

    Science.gov (United States)

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

    2016-06-09

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

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

    Directory of Open Access Journals (Sweden)

    Ksenia V. Otvagina

    2016-06-01

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

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

    Institute of Scientific and Technical Information of China (English)

    贺芳; 黄兴宇; 钱晶; 申娟

    2015-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

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

    2012-01-01

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

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

    Directory of Open Access Journals (Sweden)

    2007-06-01

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

  15. Combining ZnO/microwave treatment for changing wettability of WEEE styrene plastics (ABS and HIPS) and their selective separation by froth flotation

    Science.gov (United States)

    Thanh Truc, Nguyen Thi; Lee, Byeong-Kyu

    2017-10-01

    This study reports a simple froth flotation method to separate plastic wastes of acrylonitrile-butadiene-styrene (ABS) and high impact polystyrene (HIPS) after initial hydrophilization by coating the plastics with ZnO and microwave treatment. ABS and HIPS are typical styrene-based WEEE plastics having similar density and hydrophobicity, which hinders their separation for recycling. After coating with ZnO, 2-min microwave treatment rearranged the ABS surface and thus changed its molecular mobility and increased its hydrophilicity. The combined ZnO coating/microwave treatment facilitated the selective separation of ABS and HIPS with 100% and 95.2% recovery and 95.4% and 100% purity in froth flotation, respectively. The combination of ZnO coating-microwave treatment and froth flotation can be utilized as a selective ABS/HIPS separation technique for improved recycling of WEEE plastics.

  16. A comparison between the effects of gamma radiation and sulfur cure system on the microstructure and crosslink network of (styrene butadiene rubber/ethylene propylene diene monomer) blends in presence of nanoclay

    Science.gov (United States)

    Shoushtari Zadeh Naseri, Aida; Jalali-Arani, Azam

    2015-10-01

    Rubber blends based on (styrene-butadiene rubber (SBR)/ethylene-propylene-diene monomer (EPDM)) with and without organoclay (OC) were prepared through a melt mixing process. The concentration ratio of the rubber phases (EPDM/SBR; 50/50 wt%) and the amount of the OC were kept constant. The samples were then vulcanized by means of gamma radiation using a Co-60 gamma source as well as sulfur cure system. The effect of absorbed dose on the formation of the crosslinks was confirmed by the Fourier transform infrared spectroscopy (FTIR). The effects of absorbed dose, sulfur cure system and OC on the gel content, and crosslink density were evaluated by the chemical tests. Applying the Charlesby-Pinner equation to estimate the radiation chemical yield, revealed that the use of OC in the blend caused 20% reduction in the degradation/crosslinking ratio. Employing the swelling test data, some thermodynamic parameters were determined. Using field emission scanning electron microscopy (FE-SEM) to investigate microstructure of the samples revealed a more homogeneous structure and also an increase in compatibility of the blend components in the sample cured by the irradiation in comparison to that cured by the sulfur curing system.

  17. 丁苯透明抗冲树脂雾度影响因素的研究%Research of Influencing Factors for Haze of Styrene - butadiene Block Transparent Impact Copolymer Resin

    Institute of Scientific and Technical Information of China (English)

    高鹏; 谢云发; 孔春艳

    2012-01-01

    将抚顺的丁苯透明抗冲树脂SBC-03与美国菲利浦斯的KR-03等产品的雾度指标对比,通过对分子结构及工艺条件的分析及试验,找出了影响抚顺SBC-03雾度的因素,确定了抚顺SBC-03的适宜工艺条件,使抚顺SBC-03的雾度指标达到美国菲利浦斯产品的标准.%Haze indices of styrene - butadiene block transparent impact copolymer resin SBC-03 from Fushun petrochemical company and Phillips KR-03 from United States were compared. Through analyzing and testing their molecular structure and technological conditions, influential factors for haze of SBC-03 from Fushun petrochemical company were discovered. Finally, the suitable process condition was determined, which can make haze of Fushun SBC-03 reach to the standard of Phillips KR-03.

  18. 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.

  19. Scientific Opinion on the safety assessment of the substances (butadiene, ethyl acrylate, methyl methacrylate, styrene copolymer either not crosslinked or crosslinked with divinylbenzene or 1,3-butanediol dimethacrylate, in nanoform, for use in food contact materials

    Directory of Open Access Journals (Sweden)

    EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF

    2014-04-01

    Full Text Available This scientific opinion of the EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids deals with the safety assessment of the additives (butadiene, ethyl acrylate, methyl methacrylate, styrene copolymer either not crosslinked or crosslinked with divinylbenzene or 1,3-butanediol dimethacrylate, in nanoform, (FCM substance Nos 998, 859 and 1043, intended to be used up to 10 % w/w as an impact modifier in rigid (unplasticized polyvinylchloride (PVC. The final material is intended to be used for contact with all food types, at room temperature or lower, for long time storage. The monomers constituting the copolymer are listed in Regulation (EU 10/2011. The migration from PVC of the low molecular weight fraction of the additive below 1000 Da was estimated to be about 0.009 mg/kg food. Considering that these low molecular weight oligomers are made from authorised monomers, which by reaction are expected to lack the reactive functional groups, they do not give rise to safety concern. The migration of the additive in nanoparticle form from the PVC was estimated, using conservative migration modelling, to be about 1 x 10-6 mg/kg food and so consumer exposure would be very low, if any. The CEF Panel concluded that there is no safety concern for the consumer if the substances are used as additives individually or in combination at up to a total of 10 % w/w in rigid PVC used in contact with all food types at ambient temperature or below including long-term storage.

  20. COMPATIBILITY OF NATURAL RUBBER OF DIFFERENT CHAIN STRUCTURE WITH BUTADIENE-STYRENE RUBBER%不同链化学结构丁苯橡胶与天然橡胶混容性研究

    Institute of Scientific and Technical Information of China (English)

    马德柱; 郝文涛; 徐文总; 罗筱烈; 梁俐

    2001-01-01

    Three typical styrene-butadiene rubbers(SBR)were chosen:emulsion-SBR(ESBR)and two kinds of solution-SBR(SSBR(C)) and (SSBR(B)). Fourier transform infrared(FTIR) was used to analysis the chain structure; dynamic mechanical analysis (DMA) and differential scanning calorimeter (DSC) were used to study the compatibility of these three SBR with NR. The results show that:the blend system of SSBR(B) with NR is compatible. The blend systems of ESBR and SSBR(C) with NR exhibit two-phase morphology. The differences in compatibility among the three kinds of SBR with NR can be well explained by comparing their chain structure. The content of cis-1,4 polybutadiene (PB) in SSBR(B) is more than that in the other two SBRs and the content of 1,2-add PB is the lowest.%选择了三种丁苯橡胶(SBR)——乳聚丁苯胶(ESBR)、溶聚丁苯C(SSBR(C))及溶聚丁苯B(SSBR(B)),用红外光谱(FTIR)分析了它们的链化学结构.同时,用动态力学谱(DMA)和示差扫描量热谱(DSC)研究了这三种SBR与天然橡胶(NR)的混容性.结果表明,SSBR(B)与NR具有很好的混容性.三种SBR与NR混容性的差别,与SBR链化学结构不同有关.

  1. Preparation and properties of oil swelling polymerized styrene butadiene rubber%遇油膨胀丁苯橡胶的配方设计与性能研究

    Institute of Scientific and Technical Information of China (English)

    周爱军; 万香港; 钟毅; 田智龙; 胡凯; 江学良

    2012-01-01

    以丁苯橡胶(SBR)和自制的高吸油树脂(OAR)为主要原料,以高耐磨炭黑(HAF)为补强剂,以石油树脂为软化剂,使用物理共混方法制备遇油膨胀橡胶(OSR).兼用数学方法对其吸油性能和力学性能进行了研究,结果表明:随着高吸油树脂用量的增加,OSR的吸油性能提高,力学性能降低;随着高耐磨炭黑用量的增加,OSR的吸油性能和断裂伸长率降低,硬度和拉伸强度提高.所建立的数学方程,为预测OSR的性能及优化配方提供了理论参考.%Oil swelling rubber (OSR) was prepared by the way of physical mix, using the polymerized styrene butadiene rubber(SBR) and high oil absorption resin (OAR) as the matrix material, high abrasion furnace black (HAT) as a reinforcing agent,petroleum resin for softener. Oil absorption and mechanical properties were detected by mathematical methods. The results show that; With the amount of high oil absorbing resin increasing, oil absorption of OSR enhances but the mechanical properties decrease; with the increasing of high abrasion furnace black dosage, the oil absorption and the elongation of OSR reduce, tensile strength and hardness increase. This mathematical equation provides a theoretical basis to predict OSR performance and optimization formula.

  2. 纳米碳酸钙填充型粉末丁苯橡胶增韧改性聚氯乙烯%Nano-CaCO3 Filled Powder Styrene-Butadiene Rubber Used as Toughening Modifier for Polyvinyl Chloride

    Institute of Scientific and Technical Information of China (English)

    张周达; 陈雪梅

    2012-01-01

    Nano-CaCOa filled powder styrene-butadiene rubber was used to toughen polyvinyl chloride (PVC), the effect of the nano-CaCO3 content in compound modifier and the addition of the compound modifier on the mechanical properties of PVC was studied, and the impact fracture morphology was analyzed. The results show that the compound modifier could dramatically increase the notched impact strength of PVC. The maximum notched impact strength was 22.9 kJ · m^-2 when the mass ratio of compound modifier to PVC was 15 : 100 and the mass fraction of nano-CaCOa in compound modifier was 70%, and a typical flexible fracture morphology was found on the fracture of the notched impact sample.%将纳米碳酸钙填充型粉末丁苯橡胶作为复合改性剂用于聚氯乙烯(PVC)的增韧改性,研究了复合改性剂中纳米碳酸钙含量和复合改性剂加入量对PVC力学性能的影响,并分析了其冲击断口形貌。结果表明:复合改性剂能大幅度提高PVC的缺口冲击强度;当复合改性剂与PVC的质量比为15:100,复合改性剂中纳米碳酸钙质量分数为70%时,PVC的缺口冲击强度达到最大值22.9kJ·m^-2,缺口冲击试样断口呈典型的韧性断面形貌。

  3. Desempenho físico-químico e mecânico de concreto de cimento Portland com borracha de estireno-butadieno reciclada de pneus Physicochemical and mechanical performance of portland cement concrete with recycled styrene-butadiene tyre-rubber waste

    Directory of Open Access Journals (Sweden)

    Camila Freitas

    2009-01-01

    Full Text Available Physicochemical and mechanical techniques were carried out to characterize three concrete tyre-rubber waste dosages such as 5, 10 and 15%, w/w. The elastomeric material was identified as styrene-butadiene rubber (SBR. It was observed that the growing SBR content in the mixture decreased the concrete performance. The best results were presented by 5% w/w tyre-rubber waste concrete sample. This composition was tested at Mourão hydroelectric powerplant spillway as repairing material.

  4. Caraterização composicional do AES - um copolímero de enxertia de poli(estireno-co-acrilonitrila em poli(etileno-co-propileno-co-dieno Compositional characterization of AES a graft copolymer based on poly(styrene-co-acrylonitrile and poly(etyhlene-co-propylene-co-diene

    Directory of Open Access Journals (Sweden)

    Renato Turchet

    2006-06-01

    Full Text Available O objetivo deste trabalho é a caracterização do AES, um copolímero de enxertia de poli(estireno-co-acrilonitrila, SAN, em poli(etileno-co-propileno-co-dieno, EPDM. Para tanto, o AES foi submetido à extração seletiva de seus componentes: o SAN livre, o EDPM livre, e o copolímero de enxertia EPDM-g-SAN. O AES e suas frações foram caracterizados por espectroscopia de infravermelho, análise elementar, calorimetria diferencial de varredura e ressonância magnética nuclear, RMN¹H e RMN13C. O AES analisado apresenta a seguinte composição em massa: 65% de EPDM-g-SAN, 13% de EPDM livre e 22% de SAN livre. O EPDM apresenta 69,8% em massa de etileno, 26,5% em massa de propileno e 4,6% em massa do dieno, 2-etilideno-5-norboneno, ENB. O SAN apresenta razão em massa acrilonitrila/estireno de 28/72 e distribuição randômica de comonômeros de estireno e acrilonitrila. Estes resultados são concordantes com a composição do AES fornecida pelo fabricante, indicando que a metodologia proposta é adequada.This work aims the characterization of AES, a graft copolymer based on poly(styrene-co-acrylonitrile, SAN, and poly(etyhlene-co-propylene-co-diene, EPDM. AES was submitted to selective extraction of its components: free SAN, EPDM chains and the graft copolymer EPDM-g-SAN. AES and its fractions were characterized by infrared spectroscopy, elemental analysis, differential scanning calorimetry, 13C and ¹H nuclear magnetic resonance. The AES has 65 wt % of EPDM-g-SAN, 13 wt % of free EPDM and 22 wt % of free SAN. EPDM has 69.8 wt % of ethylene, 26.5 wt % of propylene and 4.6 wt % of diene, 2-ethylidene-5-norbonene ENB. SAN presents acrylonitrile/styrene mass ratio of 28/72 and a random distribution of acrylonitrile and styrene comonomers. These results are in agreement with the composition reported by the AES supplier, indicating that the proposed methodology is adequate.

  5. 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.

  6. Properties of a new thermoplastic elastomer-sulfonated styrene-butadiene rubber ionomers and their blends%热塑性橡胶——磺化丁苯橡胶离聚体的性能及其共混

    Institute of Scientific and Technical Information of China (English)

    敖枝平; 谢洪泉

    2001-01-01

    丁苯橡胶(SBR)作为高不饱和度的橡胶被成功地用硫酸乙酸酐作为磺化剂在石油醚及丁酮混合溶剂配成的浓溶液中磺化,并用乙酸盐中和成离聚体。研究了离聚体及其他聚合物的共混物的熔融流动性及力学性能。结果表明,SBR离聚体能很容易在硬脂酸锌存在下熔融加工,其行为象热塑性橡胶,硬脂酸锌能降低布拉本特(Brabender)混和机的扭矩所表示的熔融粘度,并增加流动活化能和离聚体的拉伸强度。离聚体的磺酸基含量能增加熔融粘度及拉伸强度。用于中和的阳离子的种类明显地影响离聚体的性能。离聚体与聚丙烯或SBS的共混物在拉伸强度上表现出协同效应,而它与聚苯乙烯或顺-1,4聚丁二烯则呈现抵消效应。%Styrene-butadiene rubber(SBR)synthesized from emulsion polymerization was sulfonated successfully by sulfuric acid and acetic anhydride in a mixed solvent of petroleum ether and methy ethyl ketone at high concentration and neutralized with metallic acetate to form ionomer.Melt flow and mechanical properties of the ionomers and of their blends with polypropylene,SBS,polystyrene or cis-1,4 polybutadiene were studied.

  7. Research progress of UV degradation of PVC/styrene-containing polymer blends%PVC/苯乙烯类聚合物共混体系紫外光降解研究进展

    Institute of Scientific and Technical Information of China (English)

    江天凯; 张军

    2013-01-01

      综述了丙烯腈-丁二烯-苯乙烯共聚物(ABS)、甲基丙烯酸甲酯-丁二烯-苯乙烯共聚物(MBS)、丙烯腈-氯化聚乙烯-苯乙烯共聚物(ACS)和丙烯腈-苯乙烯-丙烯酸酯共聚物(ASA)等苯乙烯类聚合物与聚氯乙烯共混得到的四种共混体系紫外光降解研究进展。其中,由于ABS和MBS主链结构中含有不饱和双键,在紫外光作用下易氧化降解,所以与聚氯乙烯共混体系耐候性较差;而ACS和ASA主链结构不含有不饱和双键,与聚氯乙烯的共混体系耐候性较好。%  This paper reviewed the research progress of UV degradation of poly(vinyl chloride)(PVC)/styrene-containing polymers blends. The four styrene-containing polymers were acrylonitrile-butadiene-styrene copolymer(ABS), methyl methacrylate-butadiene-styrene copolymer(MBS),acrylonitrile-chlorinated polyethy-lene-styrene copolymer(ACS) and acrylonitrile-styrene-acrylate copolymer(ASA). The reason that the PVC/ABS and PVC/MBS blends showed poor aging resistance was that there were unsaturated double bonds in the main chain of ABS and MBS and the unsaturated double bonds occurred oxidative degradation easily by UV irra-diation. On the contrary, the PVC/ACS and PVC/ASA blends showed relatively good aging resistance since there were no unsaturated double bonds in the main chain of ACS and ASA.

  8. Synthesis of High cis-Polybutadiene in Styrene Solution with Neodymium-Based Catalysts: Towards the Preparation of HIPS and ABS via In Situ Bulk Polymerization

    Directory of Open Access Journals (Sweden)

    Ramón Díaz de León

    2016-01-01

    Full Text Available In a first step, 1,3-butadiene was selectively polymerized at 60°C in styrene as solvent using NdV3/DIBAH/EASC as the catalyst system. The catalyst system activation process, the addition order of monomers and catalyst components, and the molar ratios [Al]/[Nd] and [Cl]/[Nd] were studied. The catalyst system allowed the selective 1,3-butadiene polymerization, reaching conversions between 57.5 and 88.1% with low polystyrene contents in the order of 6.3 to 15.4%. Molecular weights ranging from 39,000 to 150,000 g/mol were obtained, while cis-1,4 content was found in the interval of 94.4 to 96.4%. On the other hand, the glass transition temperatures of synthesized materials were established in the range of −101.9 to −107.4°C, explained by the presence of polystyrene segments in the polybutadiene chains; in the same sense, the polybutadienes did not show the typical melting endotherm of high cis-polybutadienes. In a second step, the resulting styrene/high cis-1,4 polybutadiene solutions were used to synthesize ABS (adding a fraction of acrylonitrile monomer and HIPS via in situ bulk polymerizations and the results were discussed in terms of morphological development, molecular parameters, dynamical mechanical behavior, and mechanical properties.

  9. Toxicologic profile of acrylonitrile.

    Science.gov (United States)

    Woutersen, R A

    1998-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1999-01-01

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

  11. Solubility parameter of poly(styrene-b-butadiene-b-styrene)

    Science.gov (United States)

    Wohlfarth, Ch.

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

  12. 聚乙烯吡咯烷酮改性氧化石墨烯对丁苯橡胶性能的影响%Effect of polyvinyl pyrrolidone modified graphene oxide on properties of styrene-butadiene rubber

    Institute of Scientific and Technical Information of China (English)

    殷标; 何俊宽; 张旭敏; 刘鹏章; 王经逸; 贾红兵

    2016-01-01

    用聚乙烯吡咯烷酮( PVP )改性氧化石墨烯( GO ),再将 PVP 改性 GO ( PGO )与丁苯橡胶(SBR)胶乳共凝制得PGO/SBR硫化胶,通过X射线衍射法(XRD)和扫描电子显微镜(SEM)分析了PGO在SBR基体中的分散状况,考察了PVP用量对SBR硫化胶性能的影响。结果表明,在PGO/SBR硫化胶中,PGO被完全剥离,均匀分散在SBR基体中;当PVP/GO(质量比)为3时,PGO/SBR硫化胶的交联密度达到最大值,比GO/SBR硫化胶增大了46.3%,物理机械性能、热稳定性能、导热性能和耐溶剂性能达到最佳,相比GO/SBR硫化胶,拉伸强度、100%定伸应力和撕裂强度分别提高了43%,315%,22%,最大分解温度升高了5.71℃,导热系数增加了11.7%,平衡溶剂吸附量下降了37.1%。%Graphene oxide ( GO ) was modified with polyvinyl pyrrolidone ( PVP ) , and then PVP modified GO ( PGO )/styrene-butadiene rubber ( SBR) vulcanizates were prepared by coagulation of PGO suspension with SBR latex. The dispersion of PGO in SBR matrix was characterized by X-ray di-ffraction and scanning electron microscope, and the effects of PVP amount on the properties of PGO/SBR vulcanizates were investigated. The results showed that PGO was completely exfoliated and dispersed homogeneously in the SBR matrix. When the mass ratio of PVP/GO was 3 , the maximum crosslinking density of PGO/SBR vulcanizates was achieved, which was increased by 46. 3% compared with that of GO/SBR vulcanizates. Meanwhile, the optimum mechanical properties, thermal stability, thermal conductivity and solvent resistance of PGO/SBR vul-canizates were obtained. The tensile strength, mo dulus at 100% and tear strength of PGO/SBR vulca-nizates were enhanced by 43%, 315% and 22%, respectively,compared with those of GO/SBR vulca-nizates . In additon, the maximum temperature of heat decomposition was improved by 5. 71 ℃, the thermal conductivity had an 11. 7% increment, the equilibrium solvent adsorption was decreased by 37. 1%.

  13. Preparation of Activated Nano-sized Kaolin Clay as Styrene Butadiene Rubber Filler%应用于橡胶补强的活性纳米高岭土制备

    Institute of Scientific and Technical Information of China (English)

    杜艳艳; 王燕民; 潘志东

    2013-01-01

    An activated nano-sized kaolin clay was prepared via an effective process with various methods such as chemical pre-intercalation, ultra-fine grinding, acid etching, drying and surface modification with cetyltrimethyl ammonium bromide (CTAB) and hydrogen silicone. The results show that the micron-sized kaolin clay that is pre-intercalated with urea is ground in a high-eneigy density stirred bead mill to prepare the nano-sized particles with the fineness of 70% < 100 nm and the lamella thickness of 10-30 nm effectively. This hybrid method could reduce the energy consumption in the preparation of the nano-sized kaolin clay, compared to the single ultra-fine grinding method. The acid etching treatment increased the specific surface area of the activated nano-sized kaolin clay without the destruction of the layered structure. The particles coated with CTAB and hydrogen silicone oil appeared a superior hydrophobicity. The azeotropic distillation drying could produce the well-dispersive activated nano-sized kaolin clay, compared to the spray drying. In addition, the as-prepared activated nano-sized kaolin clay could be used as a styrene butadiene rubber filler to improve the tensile strength and rate, and reduce the vulcanizing time.%采用化学插层-超细研磨-酸侵渍活化-干燥-表面改性的方法有效地制备了活性纳米高岭土.结果表明:通过化学插层与超细研磨的复合方法可制备70%的颗粒小于100 nm的高岭土,其片厚为10~30 nm.与单纯采用机械研磨的方法相比,该复合方法可以降低超细研磨所需的能耗.经酸侵渍活化处理可增大活性纳米高岭土的比表面积,但未破坏高岭土特有的层状结构.在活性纳米高岭土表面包覆十六烷基三甲基溴化铵和含氢硅油,可使其具有良好的亲油疏水性能.另外,对比喷雾干燥方法,经共沸蒸馏干燥的活性纳米高岭土粉体具有更好的分散性,制得的活性纳米高岭土作

  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 functional

  15. 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

  16. Effects of different cations on properties of ionomers of maleated styrene-butadiene-styrene triblock copolymer%阳离子对顺酐化苯乙烯-丁二烯-苯乙烯三嵌段共聚物离聚体性能的影响

    Institute of Scientific and Technical Information of China (English)

    刘大刚; 谢洪泉; 高玉

    2011-01-01

    The ionomers containing different cations, such as sodium, lithium, potassium, calcium,zinc, lead, magnesium, and ethyl ammonium were synthesized from the ionization of maleated styrenebutadiene-styrene triblock copolymer ( SBS ) .Effects of different cations on the thermal, mechanical, oil resistance and adhesive properties of the ionomers were studied. The results showed that, in addition to the glass transition temperatures (Tg) of butadiene and styrene blocks, the ionomers exhibited third Tg, which is due to the dissociation of the ionic domains. For the monovalent alkali metal cation neutralized ionomers, the higher the ionic potential, the higher the dissociation temperature of ionic domains, tensile strength and lap shear strength to iron plates and the order from large to small was Li+ > Na+> K+; for the divalent cation neutralized ionomers, the dissociation temperature of ionic domains decreased in the order of Ca2+> Zn2+>Pb2+ , whereas the tensile strength decreased in the order of Ca2+> Zn2 + > Mg2 + , but all were lower than those of the monovalent alkali metal cation neutralized ionomers. The oil resistance of the divalent cation neutralized ionomers was better than that of the monovalent cation neutralized ionomers or SBS.The lap shear strength of zinc ion neutralized ionomer to iron plates was the highest of all, being 0. 594 MPa.%将顺酐化苯乙烯-丁二烯-苯乙烯三嵌段共聚物(SBS)离子化得到含不同阳离子的离聚体,考察了不同阳离子对离聚体热性能、物理机械性能、耐油性能和粘接性能的影响.结果表明,离聚体有3个玻璃化转变温度(Tg),其中2个是SBS固有的Tg,另一个是离子微区的离解温度;对于含1价阳离子的离聚体,离子电离势越高,离聚体的离解温度、拉伸强度和搭接剪切强度基本越高,即从大到小依次为含锂离聚体、含钠离聚体、含钾离聚体;含2价阳离子离聚体的离解温度从大到小依次为含钙离聚

  17. 胶粉稳定苯乙烯-丁二烯-苯乙烯三嵌段共聚物改性沥青的结构与性能%Structure and properties of styrene-butadiene-styrene triblock copolymer modified asphalt stabilized by ground tire rubber

    Institute of Scientific and Technical Information of China (English)

    姚鸿儒; 周帅; 王仕峰; 张勇; 张隐西

    2015-01-01

    将苯乙烯-丁二烯-苯乙烯三嵌段共聚物(SBS)、废旧轮胎胶粉(GTR)和相容剂环氧天然橡胶(ENR)熔融共混,然后再分散到沥青中制备了 SBS/ GTR 复合改性沥青,考察了 ENR 含量、SBS/ GTR (质量比)对复合改性沥青热储存稳定性和基本性能的影响。结果表明,随着 ENR 含量的增加或 SBS含量的减少,SBS/ GTR 复合改性沥青的热储存稳定性提高,当 ENR 质量分数为1.0%、SBS/ GTR 为50/50时,复合改性沥青的热储存稳定性最佳;随着 ENR 含量的增加,SBS/ GTR 复合改性沥青的软化点、针入度、延度和黏度变化不大,但当 ENR 质量分数为10.0%时,改性沥青的软化点明显升高,针入度下降,属于一种比较硬质的改性沥青,具有较好的施工和易性;随着 SBS 含量的减少,SBS/ GTR 复合改性沥青的软化点、黏度和延度均降低。%Storage-stable styrene-butadiene-styrene triblock copolymer (SBS) / ground tire rubber (GTR) hybrid modified asphalts were prepared by dispersing the melt blend of SBS, GTR and epoxidized natural rubber (ENR) into base asphalt. Effects of ENR content, SBS/ GTR(mass ratio) on storage sta-bility, phase structure and properties were studied. The results showed that the storage stability of the modified asphalt was improved with the increase of ENR content or decrease of SBS content, and the modified asphalt achieved the best storage stability when mass fraction of ENR was 1. 0% and SBS/ GTR was 50/ 50. ENR content had a slight influence on the soften-ing points, penetration, ductility and viscosity of hybrid bind-ers, however, when the mass fraction of ENR reached 10. 0% , softening points increased and penetration decreased obviously, and the modified asphalt was hard and easy to oper-ate. The softening points, viscosity and ductility of the modi-fied asphalt all decreased with the decrease of SBS content.

  18. 苯乙烯-丁二烯-苯乙烯嵌段共聚物负载Pt催化肉桂醛制备肉桂醇的研究%Selective Hydrogenation of Cinnamaldehyde over Pt-Supported Styrene-Butadiene-Styrene Block Copolymer

    Institute of Scientific and Technical Information of China (English)

    曹云苹; 张爱清

    2011-01-01

    用紫外光交联的方法制备不同交联度的苯乙烯-丁二烯-苯乙烯嵌段共聚物(SBS)负载Pt的催化膜并探讨其对肉桂醛选择性加氢制备肉桂醇的催化效果.其中催化剂Pt纳米簇用微波法制备,XRD测其平均粒径为3.7 nm.膜载催化剂的负载量、光交联剂三羟甲基丙烷三丙烯酸酯(TMPTA)和光引发剂二苯甲酮(BP)的用量均为3%.用色谱-质谱联用、XRD、紫外分光光度计对膜载催化剂和反应产物进行了表征,结果表明,随着交联度的增加,肉桂醇的催化选择性先增后减,紫外光光照80s时,负载膜交联度23.63%,肉桂醛转化率为91.46,肉桂醇选择性80.98%.质谱分析表明交联度大于30%后,催化产物中开始有膜分解产生的小分子杂质出现,并随交联度的进一步增大而增多;显微镜检测同时说明此时膜结构发生变化,造成肉桂醇选择性的降低.%Photocrosslinked styrene-butadiene-styrene block copolymer (SBS) membrane supported nano platinum catalysts was prepared and their catalytic activity on the selective hydrogenation of cinnamaldehyde was investigated.The platinum nanoclusters with an average diameter of ca 3.7 nm were obtained by reaction of H2PtCl6 with polyols, assisted by microwave irradiation (MW).The SBS membrane was loaded with 3.0 wt% of Pt, benzophenone (BP) and 1,1,1-trimethylolpropane triacrylate (TMPTA), respectively, and varing crosslinking ratios were achieved by adjusting the radiation time.The hydrogenation products were investigated by gas chromatography and mass spectrometry (GC-MS) and UV techniques.As the crosslinking ratio increases, the selectivity for cinnamyl alcohol first increases and reaches 80.98% at a crosslinking ratio of 23.63%, and then decreases.Decomposition products of the SBS meambrane itself begin to appear as the radiaton time is over 30 min (corresponding to a crossling ratio of sightly above 30%).The deterioration of the membrane structure is also evidenced

  19. Application of Environmental Friendly Flame Retardants Made of Gray Aluminum and Boron Mud in Styrene Butadiene Rubber%硼泥、铝灰制备的环保阻燃剂在丁苯橡胶中的应用研究

    Institute of Scientific and Technical Information of China (English)

    仲维娜; 刘大晨

    2012-01-01

    以工业废料铝灰和硼泥制备主要成分为水滑石的环保阻燃剂,并将其添加到丁苯橡胶(SBR)中,研究其对阻燃性能和力学性能的影响.结果表明,随环保阻燃剂用量的增加,SBR的阻燃性能提高.使用硼泥、铝灰制备的环保阻燃剂为主的复配阻燃体系后,阻燃效果更好.但环保阻燃剂的大量使用会导致硫化胶物理机械性能下降,采用偶联剂处理后,SBR力学性能提高.%This research used the environmental friendly flame retardants which were made of some in- dustrial waste, i. e. , Gray aluminum and boron mud and had Layered Double Hydroxide (LDH) as its ma- jor component, and added these flame retardants into styrene butadiene rubber(SBR) to study its effect on the burning behaviour and mechanical characteristics on Emulsion-polymerized styrene butadiene rub- ber. The results showed that the burning behaviour of SBR was improved with increasing amount of these environmental friendly flame retardants. With the mating systems dominated by the environmental friendly flame retardants,it has very good flame residence performance. Using environmental friendly flame retard- ants in large amount will result in reduced physical and mechanical characteristics of vulcanixed rubber, then methods of modified flame retardants and reinforcement of ru6ber are taken into account to improve the mechanical properties of SBR

  20. Determination of butadiene commercial elastomers composition; Determinacao da composicao de elastomeros comerciais a base de butadieno

    Energy Technology Data Exchange (ETDEWEB)

    Tavares, M.I.B.; Mendes, L.C. [Universidade Federal, Rio de Janeiro, RJ (Brazil). Inst. de Macromoleculas

    1997-12-31

    Hydrogen-1 nuclear magnetic resonance was used in the determination of the percentile and conformational composition of commercial samples of styrene-butadiene-copolymer and poly(butadiene) homo-polymer. The results are presented and discussed 3 refs., 5 figs., 1 tab.

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

    Institute of Scientific and Technical Information of China (English)

    彭军勇; 王曦; 苏胜培

    2012-01-01

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

  2. Acrylonitrile: a suspected human carcinogen.

    Science.gov (United States)

    Koerselman, W; van der Graaf, M

    1984-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

    徐慧; 史铁钧; 孙建新; 杨兆攀

    2011-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

    董慧民; 张成龙; 彭汉修; 李再峰

    2011-01-01

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

  5. Surface modification of carbon black for the reinforcement of polycarbonate/acrylonitrile–butadiene–styrene blends

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, B.B. [School of Chemical Engineering, Fuzhou University, Fuzhou 350108 (China); Chen, Y. [School of materials Engineering, Fujian Agriculture and Forestry University, Fuzhou 350002 (China); Wang, F. [School of Chemical Engineering, Fuzhou University, Fuzhou 350108 (China); Hong, R.Y., E-mail: rhong@suda.edu.cn [School of Chemical Engineering, Fuzhou University, Fuzhou 350108 (China); College of Chemistry, Chemical Engineering and Materials Science & Key Laboratory of Organic Synthesis of Jiangsu Province, Soochow University, SIP, Suzhou 215123 (China)

    2015-10-01

    Highlights: • CB was modified through the method of oxygen plasma treatment. • Surface modified CB applied in PC/ABS blends. • The treated CB showed better compatibility in PC/ABS blends. • PC/ABS blends with treated CB showed better mechanical and thermal properties. - Abstract: The surface of carbon black was modified by oxygen plasma treatment for different times (10, 20 and 30 min). In order to increase the applicability of carbon black (CB), functional groups were grafted on the generally inert surface of CB using oxygen plasma. The surface compositional and structural changes that occurred on CB were investigated by SEM, FT-IR, Raman spectroscopy, XRD and BET. Subsequently, CB reinforced polycarbonate (PC)/acrylonitrile-butadiene-styrene (ABS) composites were prepared by internal batch mixing with the addition of different content of CB (3, 6, 9, 12 wt%). The morphology of PC/ABS/CB (7/3/6 wt%) nanocomposites was studied through scanning electron microscopy. Observations of SEM images showed that the plasma-treated CB had a better dispersion in the blend matrix. Moreover, the mechanical tests showed that the tensile strength and impact strength were improved by 32.4% and 22.5%, respectively, with the addition of plasma-treated CB. In addition, the thermal stability was improved and glass transition temperatures of both PC and ABS increased as shown by TGA and DSC, respectively.

  6. Reinforcement of Styrene-Butadiene Rubber with Silica Modified by Silane Coupling Agents: Experimental and Theoretical Chemistry Study%硅烷偶联剂改性白炭黑补强丁苯橡胶:实验和量化研究

    Institute of Scientific and Technical Information of China (English)

    任慧; 屈一新; 赵素合

    2006-01-01

    The properties of styrene-butadiene rubber (SBR) reinforced by modified silica was investigated according to national standards. Silica was modified by silane coupling agents KH-570, KH-590, and KH-792. The optimized geometries of molecular modified silica reinforced SBR were obtained by using B3LYP calculation of density functional theory with the 6-31+G basis sets. The natural bond orbital analyses were carried out. The Si-O bond length of silica modified by KH-792 was the shortest and the electronegative of O was the highest. It indicated that the connection between silica and KH-792 was the tightest. Higher tensile strength and elongation of reinforced SBR was obtained by silica modified with the KH-792. It was caused by large delocalization of lone pair electrons of the two N atoms in KH-792. The S-C bond length in silica modified by KH-590 was longer than the ordinary S-C bond length. Then the sulfur free radical (·S·) was produced more easily in vulcanization. The degree of crosslink was increased by the cross-linkage of the rubber molecule and the sulfur free radical. That was why the highest stress and tear strength of reinforced SBR was produced when silane coupling agent KH-590 was used. The calculation results was in accord with experimental data.

  7. Toxicologic profile of acrylonitrile

    NARCIS (Netherlands)

    Woutersen, R.A.

    1998-01-01

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

  8. Toxicologic profile of acrylonitrile

    NARCIS (Netherlands)

    Woutersen, R.A.

    1998-01-01

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

  9. Nanocomposites of PA6/ABS blends compatibilized with styrene-maleic anhydride copolymer;Nanocompositos de blendas de PA6/ABS compatibilizadas com copolimero estireno-anidrido maleico

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Amanda D. de, E-mail: amandaengmat@yahoo.com.b [Universidade Federal de Sao Carlos (PPG-CEM/UFSCar), SP (Brazil). Programa de Pos-Graduacao em Ciencia e Engenharia de Materiais; Araujo, Edcleide M. [Universidade Federal de Campina Grande (UFCG), PB (Brazil); Pessan, Luiz A. [Universidade Federal de Sao Carlos (DEMa/UFSCar), SP (Brazil). Dept. de Engenharia de Materiais

    2009-07-01

    To achieve a balance between stiffness and toughness, ternary nanocomposites based on blends of polyamide 6 (PA6) and acrylonitrile-butadiene-styrene (ABS) were prepared by the melt intercalation using the organoclay Cloisite{sup R} 30B (OMMT) and the styrene-maleic anhydride copolymer (SMA) as compatibilizer. Four blending sequences were used to prepare studied systems and their mechanical properties studied through the Young's modulus and notched Izod impact. It was observed that the materials prepared by all blending sequences studied showed an increase in the Young's modulus compared to the neat PA6. However, a decrease in the toughness was observed for the systems with the addition of the organoclay. The DRX results showed an intercalated structure for the some systems that used ABS in their compositions. HDT measurements of the nanocomposites showed an increase in this property compared to the neat PA6. The use of nanoclay lead to a reinforcement of the polymeric matrix. (author)

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

    OpenAIRE

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

    2012-01-01

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

  11. Intumescent flame retardant prepared by inverse suspension polymerization and its application in styrene-butadiene rubber%用反相悬浮聚合法制备膨胀型阻燃剂及其在丁苯橡胶中的应用

    Institute of Scientific and Technical Information of China (English)

    朱启龙

    2012-01-01

    The sodium polyacrylate-in situ encapsulated intumescent flame retardant ( IFR ) was prepared in the inverse suspension polymerization of sodium acrylate by adding ammonium polyphosphate, pentaerythritol and melamine, and Fourier transform infrared spectroscopy was used to characterize the structure of the flame retardant. The effects of melamine amount and the mass ratio of ammonium polyphosphate to pentaerythritol on the flame retar-dancy of styrene-butadiene rubber ( SBR ) vulcani-zates were investigated, the thermal property of flame retardant SBR was studied by thermogravime-try, and the combustion surface morphology of SBR filled with IFR was observed by scanning electron microscopy. The results showed that when the mass fraction of melamine was 3. 0% in IFR system, the mass ratio of ammonium polyphosphate to pentaerythritol was 4. 00 to 5. 67, the carbon residue yield of the system was the highest and the flame retardan-cy was better. The flame retardancy of SBR with IFR was improved correspondingly. When the IFR mass fraction was 30% in styrene-butadiene rubber vul-canizate, the oxygen index of the flame retardant rubber could achieve up to 27. 5% ; the SBR filled with IFR could form a relatively dense layer of carbon foam when it was burned, indicating that the IFR had a better intumescent flame retardant effect on SBR.%采用反相悬浮法聚合丙烯酸钠,同时将化学膨胀阻燃体系( IFR)三组分聚磷酸铵、季戊四醇和三聚氰胺加入到聚合体系中进行原位包裹,用傅里叶变换红外光谱时聚合产物的结构进行了表征,研究了三聚氰胺用量和聚磷酸铵与季戊四醇配比对丁苯橡胶硫化胶阻燃效果的影响,采用热重法分析了阻燃丁苯橡胶的热性能,并通过扫描电镜观察了添加IFR的丁苯橡胶在燃烧后表面的微现形态.结果表明,三聚氰胺的质量分数为IFR体系的3.0%、聚磷酸铵与季戊四醇的质量比为4.00~5.67时IFR体系的剩炭率最高,阻

  12. 橡胶助剂Silane-M对丁苯橡胶/白炭黑复合材料硫化性能的影响%Effect of rubber additive Silane-M on vulcanization property of styrene butadiene rubber/silica composites

    Institute of Scientific and Technical Information of China (English)

    彭华龙; 刘岚; 罗远芳; 高宏; 贾德民

    2009-01-01

    用硫化仪考察了橡胶助剂3-苯并噻唑硫代-1-丙基-三乙氧基硅烷(Silane-M)对丁苯橡胶/白炭黑复合材料硫化性能的影响.结果表明,Silane-M可明显缩短丁苯橡胶/白炭黑复合材料的正硫化时间,但不影响其焦烧时间.Silane-M具有一定的促进作用,可以加快硫化速率.未添加和添加6份(质量)Silane-M的丁苯橡胶/白炭黑复合材料在135~160 ℃的硫化温度系数和硫化反应表观活化能均比较接近,2种复合材料的硫化性能对温度的依赖性基本一致.%The effect of rubber additive 3-benzothiazolthio-1-propyl-triethoxylsilane(Silane-M) on vulcanization behavior of styrene butadiene rubber(SBR)/silica composites was investigated with rubber curometer. The results showed that Silane-M shortered vulcanization time, but had no effect on scorching time. It could accelerate rubber vulcanization process. The vulcanization temperature coefficient and apparent vulcanization activation energy of silica filled rubber without and with 6 phr Silane-M at 135-160 ℃ were approximately equal. The temperature dependence of vulcanization behavior of two kinds of composites were basically consistent.

  13. The acrylonitrile dimer ion

    Science.gov (United States)

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

    2007-04-01

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

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

    Science.gov (United States)

    Wohlfarth, Ch.

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

  15. 硬脂酸改性硅藻土及其对天然橡胶/丁苯橡胶增强性能的影响%Surface Modification of Diatomite by Steatic Acid and It's Effects on Reinforcing for Natural Rubber/Styrene Butadiene Rubber Blend

    Institute of Scientific and Technical Information of China (English)

    廖经慧; 杜高翔; 薛强; 丁浩

    2011-01-01

    Diatomite was surface modified by stearic acid. The effect of modification on the reinforcement for natural robber/styrene butadiene rubber blends (NR/SBR) was investigated by adding modified diatomite instead of amorphous silica. The activation index and sedimentation time in organic solution were examined. The mechanism of the modification was analyzed via Fourier transform infrared spectroscopy. The results indicated that the activation index of modified diatomite reached 83.0% and the sedimentation time was 5 min in kerosene when the dosage of stearic acid was 2.0% (mass fraction) of diatomite. The surface of diatomite panicles after modification appeared hydrophobic to some extent. When modified diatomite with 2.0% stearic acid was used, the tensile strength,tear strength and stress at 300% elongation of NR/SBR were increased by 14.1%, 17.8% and 40.0%, respectively, however, the elongation at break was decreased by 14.1%. There was a physical adsorption between stearic acid and diatomite.%采用硬脂酸对硅藻土进行表面改性,将改性后的硅藻土替代白炭黑添加到天然橡胶/丁苯橡胶混合物中,研究了经硬脂酸改性的硅藻土对橡胶增强性能的影响.通过活化指数和在有机溶液中的沉降时间等测试,结合Fourier红外光谱分析对硬脂酸改性硅藻土的效果和机理进行了探讨.结果表明:硬脂酸的最佳用量为2.0%(质量分数),改性后硅藻土的活化指数为83.0%,在煤油中的沉降时间为5 min,硅藻土颗粒表面呈现一定的疏水性:添加由2.0%硬脂酸改性的硅藻土后,所得橡胶制品的拉伸强度提高了14.1%,撕裂强度提高了17.8%,300%定伸应力提高了40.0%,但扯断伸长率降低了14.1%;硬脂酸与硅藻土颗粒的吸附方式为物理吸附.

  16. 环保型填充油的乳化工艺及对丁苯橡胶充油效果的影响%Emulsification process of environmental-friendly extending oil and its influence on oil-extending effect of styrene-butadiene rubber

    Institute of Scientific and Technical Information of China (English)

    李晶; 王永峰; 吴宇

    2013-01-01

    Environmental-friendly oil-extended styrene-butadiene rubber ( SBR) was prepared with high Mooney viscosity SBR 1723 latex and environmental-friendly extending oil in which the mass fraction of polycyclic aromatic hydrocarbons was less than 3. 0% as materials, and the influences of emulsification process on emulsification effect of extending oil and properties of environmental-frendly oil-extended SBR were investigated. The results showed that the properties of the obtained environmental-friendly oil-extended SBR met the requirements of technical indicators under the conditions of emulsifying temperature 70 ℃ , extending oil/water/emulsi-fier (mass ratio) 100/200/2, stirring rate of agglomeration 163 r/min, agglomerating temperature 65 -70℃ when the emulsification process was used, by which the emulsifier disproportionated rosin acid soap was added into extending oil and stirred first and then the water was added.%以高门尼黏度丁苯橡胶(SBR) 1723基础胶浆和稠环芳烃质量分数低于3.0%的环保型橡胶填充油为原料制备环保型充油SBR,考察了乳化工艺对填充油乳化效果的影响以及所制得的环保型充油SBR的性能.结果表明,在以歧化松香酸钾皂为乳化剂、先将乳化剂加入填充油中搅拌一段时间后再加入水的油乳化方式、油乳化温度为70℃、填充油/水/乳化剂(质量比)为100/200/2以及凝聚时搅拌转速为163r/min、凝聚温度为65~70℃的条件下,所得产品的各项性能指标满足产品标准的要求.

  17. 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

  18. 不同环保型操作的性质及对乳聚丁苯橡胶性能的影响%Properties of different environmental-friendly processing oils and their influences on properties of emulsion polymerized styrene-butadiene rubber

    Institute of Scientific and Technical Information of China (English)

    胡海华; 刘春芳; 赵洪国; 吴宇; 何连成; 李波

    2013-01-01

    分析了牌号为NAP-10和AP 15以及处理的馏出芳烃抽出物(TDAE)的性质,考察了以其作操作油对乳聚丁苯橡胶(ESBR)门尼黏度、硫化特性、力学性能、耐老化性能、耐磨性能以及制品外观的影响,并与芳烃油作操作油进行了对比.结果表明,NAP-10、TDAE和AP 15中的多环芳烃质量分数均小于3.00%,属于环保型操作油.3种环保型操作油对ESBR的软化能力和加工安全性均高于芳烃油.采用3种环保型操作油制备的ESBR硫化胶的力学性能、耐老化性能和耐磨性能略逊于以芳烃油为操作油的硫化胶,且放置一段时间后橡胶制品均有油品析出现象,随着操作油中芳烃含量的增加,油品析出减少,其中用AP 15作操作油制备的硫化胶的耐磨性能和制品外观最好.%The properties of brand NAP-10, AP 15 and triple distillate aromatic extracts (TDAE) were analyzed, their influences as processing oils on properties, such as Mooney viscosity, curing characteristics, mechanical properties, aging resistance and abrasion resistance as well as appearance of manufactures of emulsion polymerized styrene-butadiene rubber ( ESBR ) were investigated and compared with those of aromatic oil as processing oil. The results showed that the mass fraction of polycy-clic aromatic hydrocarbons in NAP-10, AP 15 and TDAE were less than 3. 00% , so they were all environmental-friendly processing oils. The softening ability and processing safety when using these three as processing oil of ESBR were higher than those of aromatic oil as processing oil. The mechanical properties, aging resistance and abrasion resistance of ESBR vulcanizates with the three kinds of environmental-friendly processing oils were inferior to those of ESBR vulcanizates with aromatic oil, and there were oil stains on surface of ESBR manufactures after stored for a period, the phenomenon decreased with increasing aromatics content in the processing oils. The abrasion resistance

  19. POLYMER-SUPPORTED LANTHANIDE COMPLEXES FOR THE POLYMERIZATION OF BUTADIENE

    Institute of Scientific and Technical Information of China (English)

    YU Guangqian; LI Yuliang; LIU Chongming

    1992-01-01

    The characteristics of styrene-acrylic acid copolymer supported lanthanide complexes(SAAC Ln)(Ln=La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu) were described.butadiene, a peak in activity appeared at Nd and Pr, Sm, Eu and the heavy lanthanides exhibited low or no activities. The effects of some factors on the activities were discussed. The microstructure of the polymers obtained with all the lanthanides in the series were the same and the content of cis-1,4 polybutadiene attained was more than 98%.

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

    NARCIS (Netherlands)

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

    1997-01-01

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

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

    NARCIS (Netherlands)

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

    1997-01-01

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

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

    NARCIS (Netherlands)

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

    1996-01-01

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

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

    NARCIS (Netherlands)

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

    1995-01-01

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

  4. Biobased synthesis of acrylonitrile from glutamic acid

    NARCIS (Netherlands)

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

    2011-01-01

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

  5. Biobased synthesis of acrylonitrile from glutamic acid

    NARCIS (Netherlands)

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

    2011-01-01

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

  6. 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.

  7. Species differences in metabolism of 1,3-butadiene

    Energy Technology Data Exchange (ETDEWEB)

    Henderson, R.F.

    1995-02-01

    1,3-Butadiene (BD) is a 4-carbon gaseous compound with two double bonds. Used in high tonnage to make styrene-butadiene polymers in the rubber industry. Because of large amounts in use, BD was tested for toxicity in 2-year inhalation exposures of both Sprague-Dawley rats and B6C3F{sub 1} mice. The results of the two-species studies were dramatically different. In the initial study in mice, BD was shown to be a potent multiple-site carcinogen at exposure levels of 625 and 1250 ppM. There were increased incidences of neoplasia in the heart, lung, mammary gland, and ovary; malignant lymphomas resulted in early deaths of the mice so that the planned 2-year study was stopped after only 61 weeks of exposure. The second study in mice was conducted at much lower exposure concentrations (6.25, 20, 62.5, 200, and 625 ppM) and lasted 104 weeks. Increased incidences of hemangiosarcomas of the heart and lung neoplasia were observed in males exposed to 62.5 ppM BD, while females had increased lung neoplasia even at the 6.25 ppM exposure level. Early deaths from lymphomas were again observed at the high exposure concentration (625 ppm). A noncancer toxicity observed in mice was a macrocytic, megaloblastic anemia.

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

    Science.gov (United States)

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

    2012-01-01

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

  9. 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.

  10. Biological monitoring of acrylonitrile exposure

    Energy Technology Data Exchange (ETDEWEB)

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

    1982-01-01

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

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

    Science.gov (United States)

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

    2006-10-01

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

  12. Starch Modification by Graft Copolymerization of Acrylonitrile

    Institute of Scientific and Technical Information of China (English)

    刘瑞贤; 李莉; 茹宗玲; 张黎明; 高建平; 田汝川

    2003-01-01

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

  13. Organic chemistry. A rhodium catalyst for single-step styrene production from benzene and ethylene.

    Science.gov (United States)

    Vaughan, Benjamin A; Webster-Gardiner, Michael S; Cundari, Thomas R; Gunnoe, T Brent

    2015-04-24

    Rising global demand for fossil resources has prompted a renewed interest in catalyst technologies that increase the efficiency of conversion of hydrocarbons from petroleum and natural gas to higher-value materials. Styrene is currently produced from benzene and ethylene through the intermediacy of ethylbenzene, which must be dehydrogenated in a separate step. The direct oxidative conversion of benzene and ethylene to styrene could provide a more efficient route, but achieving high selectivity and yield for this reaction has been challenging. Here, we report that the Rh catalyst ((Fl)DAB)Rh(TFA)(η(2)-C2H4) [(Fl)DAB is N,N'-bis(pentafluorophenyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene; TFA is trifluoroacetate] converts benzene, ethylene, and Cu(II) acetate to styrene, Cu(I) acetate, and acetic acid with 100% selectivity and yields ≥95%. Turnover numbers >800 have been demonstrated, with catalyst stability up to 96 hours.

  14. 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.

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

    Science.gov (United States)

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

    2016-08-01

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

  16. Cancer occurrence among workers exposed to acrylonitrile.

    Science.gov (United States)

    Rothman, K J

    1994-10-01

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

  17. 21 CFR 177.1040 - Acrylonitrile/styrene copoly-mer.

    Science.gov (United States)

    2010-04-01

    ... this section may contain adjuvant substances required in their production, with the exception that they...: Substances Limitation Condensation polymer of toluene sulfonamide and formaldehyde 0.15 pct maximum. (c...

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

    Science.gov (United States)

    2007-01-01

    thickness. The copolymer samples were dissolved in a toluene, a neutral solvent, in a 3.0 wt % concentration. Approximately 0.1 wt % Irganox 1010 ...self- assembled microstructure on the nanometer scale, which has led to applications in membranes, templates for nanoparticle synthesis , photonic

  19. The influence of UV aging of a styrene/butadiene/styrene modified bitumen: comparison between laboratory and on site aging

    Energy Technology Data Exchange (ETDEWEB)

    Francoise Durrieu; Fabienne Farcas; Virginie Mouillet [Service Physico-chimie des Materiaux, Paris (France). Laboratoire Central des Ponts et Chaussees

    2007-07-15

    During the service life in a pavement, neat bitumen and modified bitumen age as the result of the mixing with aggregates, the process of laying, the climatic conditions and the traffic. Laboratory methods for simulating the short-term and long-term ageing (RTFOT and PAV, respectively) are standardized. None of them takes into account the influence of UV radiations. In the particular case of a pavement located in south France, a comparison is drawn through Fourier Transformed InfraRed (FTIR) analysis. Three types of ageing are compared: the standard simulated ageings, the actual on site ageing after 12 and 26 months of road service and the ageing when UV exposure in a weathering oven follows RTFOT simulation. According to carbonyle function evolution by FTIR spectroscopy, this work shows that for all tested binders, the same ageing level as the one simulated by PAV is reached in a few hours when a thin film of binder is submitted to UV exposure after RTFOT. It is also to be noted that the level of the on site ageing of a SBS Polymer modified Bitumen (PmB) reaches the simulated PAV ageing after 12 months of pavement life. 23 refs., 7 figs., 4 tabs.

  20. A NOVEL ACRYLONITRILE DERIVATIVE HAVING PHOTOVOLTAIC PERFORMANCE

    Directory of Open Access Journals (Sweden)

    Cigdem Yorur-Goreci

    2016-10-01

    Full Text Available A new acrylonitrile derivative 3 (BPCPFA which offer potential application as organic solar cell material was synthesized with three steps. The structures of the molecules synthesized in these steps were characterized using various spectral analyses. BPCPFA was investigated as an electron acceptor molecule in next generation organic solar cells. Theoretical prediction and experimental studies for photovoltaic performance were performed. Based on these results, it is concluded that BPCPFA with extended conjugated system has good and promising photovoltaic performance with Voc value as 0.96 V.

  1. Investigation of protein-styrene oxide adducts as a molecularbiomarker of human exposed to styrene

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Hemoglobin-styrene oxide adducts in blood has been studied as a molecular biomarker of worker exposed to styrene.Determination of protein-styrene oxide adducts in different biological samples with modified Raney-Ni procedure is described in this paper. The following biological samples have been investigated: fresh rat blood reacted with styrene oxide in vitro; rat blood reacted with styrene or styrene oxide in vivo; vein blood from workers exposed to styrene in two factories. The data showed that there was a good linear dose-response relationship between reacting dose of styrene oxide or styrene and amount of protein-styrene oxide adducts in both in vitro and in vivo experiments. For human samples, a dose-response relationship between protein adducts and styrene exposure can be found in glass fiber factory, but not in piano manufacture plant.

  2. A VUV photoionization study of the multichannel reaction of phenyl radicals with 1,3-butadiene under combustion relevant conditions.

    Science.gov (United States)

    Golan, Amir; Ahmed, Musahid; Mebel, Alexander M; Kaiser, Ralf I

    2013-01-07

    We studied the reaction of phenyl radicals (C(6)H(5)) with 1,3-butadiene (H(2)CCHCHCH(2)) exploiting a high temperature chemical reactor under combustion-like conditions (300 Torr, 873 K). The reaction products were probed in a supersonic beam by utilizing VUV radiation from the Advanced Light Source and by recording the experimental PIE curves at mass-to-charge ratios of m/z = 130 (C(10)H(10)(+)), 116 (C(9)H(8)(+)), and 104 (C(8)H(8)(+)). Our data suggest that the atomic hydrogen (H), methyl (CH(3)), and vinyl (C(2)H(3)) losses are open with estimated branching ratios of about 86 ± 4%, 8 ± 2%, and 6 ± 2%, respectively. The isomer distributions were probed further by fitting the experimentally recorded PIE curves with a linear combination of the PIE curves of individual C(10)H(10), C(9)H(8), and C(8)H(8) isomers. These fits indicate the formation of three C(10)H(10) isomers (trans-1,3-butadienylbenzene, 1,4-dihydronaphthalene, 1-methylindene), three C(9)H(8) isomers (indene, phenylallene, 1-phenyl-1-methylacetylene), and a C(8)H(8) isomer (styrene). A comparison with results from recent crossed molecular beam studies of the 1,3-butadiene-phenyl radical reaction and electronic structure calculations suggests that trans-1,3-butadienylbenzene (130 amu), 1,4-dihydronaphthalene (130 amu), and styrene (104 amu) are reaction products formed as a consequence of a bimolecular reaction between the phenyl radical and 1,3-butadiene. 1-Methylindene (130 amu), indene (116 amu), phenylallene (116 amu), and 1-phenyl-1-methylacetylene (116 amu) are synthesized upon reaction of the phenyl radical with three C(4)H(6) isomers: 1,2-butadiene (H(2)CCCH(CH(3))), 1-butyne (HCCC(2)H(5)), and 2-butyne (CH(3)CCCH(3)); these C(4)H(6) isomers can be formed from 1,3-butadiene via hydrogen atom assisted isomerization reactions or via thermal rearrangements of 1,3-butadiene involving hydrogen shifts in the high temperature chemical reactor.

  3. Palladium phosphine complexes for the telomerization of butadiene

    DEFF Research Database (Denmark)

    2010-01-01

    A phosphine ligand suitable for use in telomerizing butadiene comprises two phenyl groups and a xanthene moiety.......A phosphine ligand suitable for use in telomerizing butadiene comprises two phenyl groups and a xanthene moiety....

  4. CHARACTERIZATION OF IRON COMPLEXES SUPPORTED ON POLYMER AND THEIR CATALYTIC ACTIVITY IN BUTADIENE POLYMERIZATION

    Institute of Scientific and Technical Information of China (English)

    YU Guangqian; LI Yuliang; YANG Zhifan; WANG Hong

    1990-01-01

    Styrene-acrylic acid copolymer (SAAC)-supported iron complex (SAAC·Fe)was characterized and the effect of the characteristic parameters on the catalytic activity of the complex was investigated. IR spectrum suggested that the complex SAAC·Fe possesses a structure of(C) and the Fe-O bond is higher in covalency. R-C-O-Fe-O-Fe(C) The complex SAAC Fe with the structure of(C) showed a higher catalytic activity in butadiene polymerization. When Fe/- COOH molar ratio in SAAC·Fe was about 0.2 the complex gave optimum catalytic activity. The catalytic activity of SAAC Fe with the higher content of long sequence of acrylic acid units was low. When the content of the short sequence of acrylic acid units was predominant and at the same time the content of the short sequence was approximately equal to that of the long sequence for stryrene, the activity of the complex was high.

  5. 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.

  6. Low temperature decomposition of styrene-butadiene rubber and used tire

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Won Il; Hong, In Kwon [Department of Chemical Engineering, Dankook University, Seoul (Korea); Kim, Hyung Jin [Department of Environmental and Civil Engineering, Kimpo College, Kimpo (Korea)

    2000-04-01

    The disposal of automotive tires is an increasing environmental and economic problem but few methods have been proposed to tackle the problematic wastes in a systematic and efficient way. Therefore there is a demand for new recycling systems for automotive tires. Tire and raw material of tire i.e., SBR were degraded using supercritical fluid (SCF) process that is the low temperature degradation process relative to the convectional thermal degradation process. The oil yield was increased and that of char was decreased with the increased reaction temperature and pressure in SCF process. Byt the effect of temperature was larger than those of pressure. The oil yields of tire were 33.8-59.2% and 49.1-72.8% using THF and benzene respectively. So, benzene was suitable solvent in SCF process. The number average molecular weights of SBR and tire were decreased with the increased reaction time and temperature. The oil components were mostly 20 aromatic compounds. The optimum condition of SCF process was 320 degree C, 4000 psi in the case of benzene as a supercritical fluid. 16 refs., 9 figs., 2 tabs.

  7. 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...

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

    Directory of Open Access Journals (Sweden)

    Viktor F. Vargalyuk

    2016-03-01

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

  9. Mutagenicity, carcinogenicity, and teratogenicity of acrylonitrile.

    Science.gov (United States)

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

    1999-05-01

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

  10. Thermodynamics of coil-hyperbranched poly(styrene-b-acrylated epoxidized soybean oil) block copolymers

    Science.gov (United States)

    Lin, Fang-Yi; Hohmann, Austin; Hernández, Nacú; Cochran, Eric

    Here we present the phase behavior of a new type of coil-hyperbranched diblock copolymer: poly(styrene- b-acrylated epoxidized soybean oil), or PS-PAESO. PS-PAESO is an example of a biorenewable thermoplastic elastomer (bio-TPE). To date, we have shown that bio-TPEs can be economical commercial substitutes for their petrochemically derived analogues--such as poly(styrene- b-butadiene- b-styrene) (SBS)--in a range of applications including pressure sensitive adhesives and bitumen modification. From a polymer physics perspective, PS-PAESO is an interesting material in that it couples a linear coil-like block with a highly branched block. Thus in contrast to the past five decades of studies on linear AB diblock copolymers, coil-hyperbranched block copolymers are relatively unknown to the community and can be expected to deviate substantially from the standard ``universal'' phase behavior in the AB systems. To explore these new materials, we have constructed a library of PS-PAESO materials spanning a range of molecular weight and composition values. The phase transition behavior and the morphology information will be interpreted by isochronal temperature scanning in dynamic shear rheology, small angle X-ray scattering and the corresponding transmission electron microscopy.

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

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Nitrile rubber modified acrylonitrile-methyl... Nitrile rubber modified acrylonitrile-methyl acrylate copolymers. Nitrile rubber modified acrylonitrile... this chapter, subject to the provisions of this section. (a) For the purpose of this section, nitrile...

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

    Institute of Scientific and Technical Information of China (English)

    Li Zhengguang

    2008-01-01

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

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

    Science.gov (United States)

    Choi, Seong-Ho; Nho, Young Chang

    2000-04-01

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

  14. Helbredsrisici ved eksponering for styren i glasfiberplastindustrien

    DEFF Research Database (Denmark)

    Kolstad, Henrik Albert; Ebbehøj, Nielse; Bonde, Jens Peter

    2012-01-01

    or relevant exposure levels. We recommend reconsideration of the current Danish threshold limit value of 25 ppm, biological monitoring of styrene exposed workers, and epidemiological analyses of styrene exposure levels and long-term health effects among employees of the Danish reinforced plastics industry....

  15. Polyacrylamide polymers derived from acrylonitrile without intermediate isolation

    Energy Technology Data Exchange (ETDEWEB)

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

    1977-04-05

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

  16. Helbredsrisici ved eksponering for styren i glasfiberplastindustrien

    DEFF Research Database (Denmark)

    Kolstad, Henrik Albert; Ebbehøj, Nielse; Bonde, Jens Peter;

    2012-01-01

    This is a summary of the health risks of occupational styrene exposure based on recent reviews. We conclude about the exposure levels that there is strong evidence that styrene causes acute irritation of eyes and respiratory tract above 25 ppm, genotoxic effects above 10 ppm, and persistent nervous...... system effects with for instance reduced psychological performance, colour discrimination and hearing level following long-term styrene exposure above 10 ppm. There is moderate evidence of a causal association with cancer, but data are not sufficient to allow us to pinpoint specific cancers at risk...

  17. Laboratory-scale biofiltration of acrylonitrile by Rhodococcus rhodochrous DAP 96622 in a trickling bed bioreactor.

    Science.gov (United States)

    Zhang, Jie; Pierce, George E

    2009-07-01

    Acrylonitrile (ACN), a volatile component of the waste generated during the production of acrylamide, also is often associated with aromatic contaminants such as toluene and styrene. Biofiltration, considered an effective technique for the treatment of volatile hydrocarbons, has not been used to treat volatile nitriles. An experimental laboratory-scale trickling bed bioreactor using cells of Rhodococcus rhodochrous DAP 96622 supported on granular activated carbon (GAC) was developed and evaluated to assess the ability of biofiltration to treat ACN. In addition to following the course of treatability of ACN, kinetics of ACN biodegradation during both recycle batch and open modes of operation by immobilized and free cells were evaluated. For fed-batch mode bioreactor with immobilized cells, almost complete ACN removal (>95%) was achieved at a flow rate of 0.1 microl/min ACN and 0.8 microl/min toluene (TOL) (for comparative purposes this is equivalent to 6.9 mg l(-1) h(-1) ACN and 83.52 mg l(-1) h(-1) TOL). In a single-pass mode bioreactor with immobilized cells, at ACN inlet loads of 100-200 mg l(-1) h(-1) and TOL inlet load of approximately 400 mg l(-1) h(-1), with empty bed retention time (EBRT) of 8 min, ACN removal efficiency was approximately 90%. The three-dimensional structure and characteristics of the biofilm were investigated using confocal scanning laser microscopy (CSLM). CLSM images revealed a robust and heterogeneous biofilm, with microcolonies interspersed with voids and channels. Analysis of the precise measurement of biofilm characteristics using COMSTAT agreed with the assumption that both biomass and biofilm thickness increased along the carbon column depth.

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

    Institute of Scientific and Technical Information of China (English)

    甘永胜; 顾军民; 方永成

    2004-01-01

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

  19. Design, synthesis and physical properties of poly(styrene–butadiene–styrene)/poly(thiourea-azo-sulfone) blends

    Indian Academy of Sciences (India)

    Ayesha Kausar

    2014-06-01

    A new aromatic azo-polymer, poly(thiourea-azo-sulfone), has been synthesized using 1-(4-thiocarbamoylaminophenylsulfonylphenyl)thiourea and diazonium salt solution. Conducting and thermally stable rubbery blends of poly(styrene-block-butadiene-block-styrene) (SBS) triblock copolymer and poly(thiourea-azo-sulfone) (PTAS) were produced by solution blending technique. PTAS possessed fine solubility in polar solvents and high molar mass 63 × 103 g moL-1. Microscopic analysis on SBS/PTAS blends revealed good adhesion between the two polymers without macro phase separation. Electrical conductivity measurement recommended that blending of SBS with 60% PTAS was sufficiently conducting 1.43 S cm-1. A relationship between PTAS loading and thermal stability of blends was observed. With the increasing PTAS content, 10% gravimetric loss was increased from 481 to 497 °C, while glass transition improved from 123 to 136 °C (better than neat SBS but lower than PTAS). The blends also established higher tensile strength (52.40–59.96 MPa) relative to SBS. Fine balance of properties renders new SBS/PTAS, potential engineering plastics for a number of aerospace relevance.

  20. Radiation initiated copolymerization of allyl alcohol with acrylonitrile

    Energy Technology Data Exchange (ETDEWEB)

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

    1996-07-01

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

  1. Radiation initiated copolymerization of allyl alcohol with acrylonitrile

    Science.gov (United States)

    Şolpan, Dilek; Güven, Olgun

    1996-07-01

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

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

    Institute of Scientific and Technical Information of China (English)

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

    2008-01-01

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

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

    OpenAIRE

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

    2014-01-01

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

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

    Science.gov (United States)

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

    2011-01-01

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

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

    NARCIS (Netherlands)

    Saggiomo, V.; Velders, A.H.

    2015-01-01

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

  6. Evaluation of the Impact of an Additive Manufacturing Enhanced CubeSat Architecture on the CubeSat Development Process

    Science.gov (United States)

    2016-09-15

    fabrication method ideally suited to low- quantity, highly customized builds, leading to interest in the application of AM techniques to satellite...x List of Acronyms and Definitions ...................................................................................... xi...of Acronyms and Definitions 1U 10 cm x 10 cm x 10cm, unit volume size for CubeSats 3D Three-Dimensional ABS Acrylonitrile Butadiene Styrene ABS-M20

  7. 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,...

  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. STUDIES ON MICELLE BEHAVIORS OF STYRENE-BUTADIENE-STYRENE (SBS) TRIBLOCK COPOLYMERS IN METHYL ETHYL KETONE (MEK) BY POSITRON ANNIHILATION TECHNIQUE

    Institute of Scientific and Technical Information of China (English)

    YANG Rongjie; YE Meiling; SHI Lianghe; WANG Yunyu

    1992-01-01

    Positron annihilation technique was used to study the micelle behaviors of two SBS triblock copolymers in MEK solvent at different temperatures. Annihilation lifetime τ3 of ortho-positronium(o-Ps) exhibited an obvious transition from shorter lifetime to longer lifetime with temperature. It was attributed to the change of micelle behavior of SBS copolymer molecules in the solution. Experimental results of sedimentation velocity of ultracentrifuge were also reported.

  10. Organocatalytic atroposelective synthesis of axially chiral styrenes

    Science.gov (United States)

    Zheng, Sheng-Cai; Wu, San; Zhou, Qinghai; Chung, Lung Wa; Ye, Liu; Tan, Bin

    2017-05-01

    Axially chiral compounds are widespread in biologically active compounds and are useful chiral ligands or organocatalysts in asymmetric catalysis. It is well-known that styrenes are one of the most abundant and principal feedstocks and thus represent excellent prospective building blocks for chemical synthesis. Driven by the development of atroposelective synthesis of axially chiral styrene derivatives, we discovered herein the asymmetric organocatalytic approach via direct Michael addition reaction of substituted diones/ketone esters/malononitrile to alkynals. The axially chiral styrene compounds were produced with good chemical yields, enantioselectivities and almost complete E/Z-selectivities through a secondary amine-catalysed iminium activation strategy under mild conditions. Such structural motifs are important precursors for further transformations into biologically active compounds and synthetic useful intermediates and may have potential applications in asymmetric synthesis as olefin ligands or organocatalysts.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-01-03

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

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

    OpenAIRE

    Jiu Huang; Zhengfu Bian; Shaogang Lei

    2015-01-01

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

  13. 46 CFR 154.1750 - Butadiene or vinyl chloride: Refrigeration system.

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Butadiene or vinyl chloride: Refrigeration system. 154... and Operating Requirements § 154.1750 Butadiene or vinyl chloride: Refrigeration system. A refrigeration system for butadiene or vinyl chloride must not use vapor compression unless it: (a) Avoids...

  14. Effects of polystyrene-b-poly(aminomethyl styrene)s as stabilizers on dispersion polymerization of styrene in alcoholic media.

    Science.gov (United States)

    Itoh, Tomomichi; Fukutani, Kaori; Hino, Masato; Ihara, Eiji; Inoue, Kenzo

    2009-02-15

    The effects of polystyrene-b-poly(aminomethyl styrene) (PS(n)-b-PAMS(m)) stabilizers on the particle size (D(n)) and size distribution (PSD) in dispersion polymerization of styrene were investigated. The block copolymers, PS(n)-b-PAMS(m), were prepared as follows: (i) atom transfer radical polymerization (ATRP) of styrene (PS-Br), (ii) ATRP of vinylbenzylphthalimide with the PS-Br (PS-b-PVBP), and (iii) treatment of the PS-b-PVBP with hydrazine. When the dispersion polymerization of styrene proceeded at 60 degrees C in ethanol with PS(19)-b-PAMS(130) stabilizer, spherical polystyrene particles with D(n)=0.91 microm (PSD=1.01) were obtained. The particle size was strongly affected by the copolymer composition. With an increase in PAMS block length from m=54 to 100 in PS(17)-b-PAMS(m), particle diameter became smaller from 1.55 to 0.91 microm. On the other hand, an increase in the length from m=20 to 82 in PS(34)-b-PAMS(m)s caused an increase in particle size from 0.35 to 0.70 microm. Titration of the particles suggests that 14-81% of stabilizers used in the polymerization system were attached on the polystyrene particle surfaces, depending on the composition of the block copolymers. Thus, for the dispersion polymerization of styrene, PS(n)-b-PAMS(m) block copolymers have both functions as a stabilizer during polymerization and surface-modification sites of polystyrene particles.

  15. Palladium-Catalyzed Intramolecular Aminofluorination of Styrenes%Palladium-Catalyzed Intramolecular Aminofluorination of Styrenes

    Institute of Scientific and Technical Information of China (English)

    徐涛; 邱水发; 刘国生

    2011-01-01

    A novel palladium-catalyzed intramolecular oxidative aminofluorination of styrenes has been developed by using NFSI as fluorinating reagent. This reaction represented an efficient method for the synthesis of 2-aryl-3-fluoropyrrolidine derivatives.

  16. Rh-catalyzed linear hydroformylation of styrene

    NARCIS (Netherlands)

    Boymans, E.; Janssen, Michèle; Müller, Christian; Lutz, M.|info:eu-repo/dai/nl/304828971; Vogt, D.

    2012-01-01

    Usually the Rh-catalyzed hydroformylation of styrene predominantly yields the branched, chiral aldehyde. An inversion of regioselectivity can be achieved using strong π-acceptor ligands. Binaphthol-based diphosphite and bis(dipyrrolyl-phosphorodiamidite) ligands were applied in the Rh-catalyzed hydr

  17. 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.)

  18. 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.

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

    Science.gov (United States)

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

    2002-07-01

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

  20. 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.

  1. 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.

  2. 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.

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

    Science.gov (United States)

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

    2015-07-01

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

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

    OpenAIRE

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

    2011-01-01

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

  5. 共聚物-深剂体系的气液平衡:新UNIFAC基团热力学模型与实验研究%Vapor-Liquid Equilibrium of Copolymer+solvent Systems:Experimental Data and Thermodynamic Modeling with New UNIFAC groups

    Institute of Scientific and Technical Information of China (English)

    Rogério A.G. Sé; Martín Aznar

    2008-01-01

    Vapor-liquid equilibrium (VLE)data for copolymer solutions are necessary for several chemical processes.However,VLE data for copolymer solutions in the published report are rare.In this study.experimental VLE data for binary systems copolymer+solvent were obtained using a gravimetric-sorption apparatus.The studied systems were hexane+poly(21%acrylonitrile-co-butadiene),hexanc+poly(33%acrylonitrile-co-butadiene),hexane+poly(51%acrylonitrile-co-butadiene),hexanc+poly(23%styrene-co-butadiene),hexane+poly(45%styrene-co-butadiene),and benzene+poly(44%styrene-co-methyl methacrylate)in the range 50-70℃.The experimental data were correlated with the UNIFAC and Elbro-FV group contribution models for the activity coefficient.Two sets of functional groups had been used to represent the monomers in copolymers:literature groups and new proposed groups.The mean deviations between experimental and calculated mass fractions about 2.4%with ElbroFV and 13.3%witll Zhong were observed when the groups proposed in this study were USed.and of 3.5%for E1bro-FV and 13.2%for Zhong when literature groups were used.

  6. Recycling tires? Reversible crosslinking of poly(butadiene).

    Science.gov (United States)

    Trovatti, Eliane; Lacerda, Talita M; Carvalho, Antonio J F; Gandini, Alessandro

    2015-04-01

    Furan-modified poly(butadiene) prepared by the thiol-ene click reaction is crosslinked with bismaleimides through the Diels-Alder reaction, giving rise to a novel recyclable elastomer. This is possible because of the thermal reversibility of the adducts responsible for the formation of the network. The use of this strategy provides the possibility to produce recyclable tires.

  7. A risk assessment for acrylonitrile in consumer products.

    Science.gov (United States)

    Johnston, P K; Rock, A R

    1990-12-15

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

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

    Science.gov (United States)

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

    2014-06-01

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

  9. BARRIER PROPERTY AND STRUCTURE OF ACRYLONITRILE/ACRYLIC COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    YANG Zhenghua; LI Yuesheng

    1997-01-01

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

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

    Science.gov (United States)

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

    2014-10-01

    In this work, a membrane dispersion microreactor was utilized for the hydration of acrylonitrile to produce acrylamide. Through observation using a microscopy, it was found that the acrylonitrile was dispersed into the continuous phase (the aqueous phase contains nitrile hydratase (NHase)) as droplets with a diameter ranged from 25 to 35 μm, hence the mass transfer specific surface area was significantly increased, and the concentration of acrylamide reached 52.5 wt% within 50 min. By contrast, in stirred tanks, the concentration of acrylamide only got 39.5 wt% within 245 min. Moreover, only a few amounts of acrylonitrile were accumulated in this microreactor system. Through optimizing the flow rate, the concentration of acrylamide reached 45.8 wt% within 35 min, the short reaction time greatly weakened the inhibition of acrylonitrile and acrylamide on the enzyme activity, which is suitable for prolonging the life of free cell. Copyright © 2014 Elsevier Ltd. All rights reserved.

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

    Institute of Scientific and Technical Information of China (English)

    WU Chinyung

    1983-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

    WANG Bing; XIE Shishan; CAO Mengjiun

    1987-01-01

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

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

    Science.gov (United States)

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

    2011-01-01

    We synthesized three novel highly fluorescent compounds, 2-(2’-pyridyl)-3-(N-ethyl-(3’-carbazolyl))acrylonitrile, 2-(3”-pyridyl)-3-(N-ethyl-(3’-carbazolyl))acrylonitrile, and 2-(4-pyridyl)-3-(N-ethyl-(3’-carbazolyl))acrylonitrile by Knoevenagel condensation. The first two were synthesized without solvent in the presence of piperidine as a catalyst; the third was synthesized without a catalyst and with N,N-dimethylformamide as a solvent. In solution, the molar absorption coefficients showed absorptions at 380, 378, and 396 nm, respectively; in solid state, absorptions were at 398, 390, and 442 nm, respectively. The fluorescence emission was at 540, 540 and 604 nm, respectively, the 2-(4-pyridyl)-3-(N-ethyl-(3’-carbazolyl))acrylonitrile showed a red shift in the emission of 64 nm compared to the other two compounds. The fluorescence quantum yield for the compounds in powder form showed values of 0.05, 0.14, and 0.006, respectively; compared with the value measured for the Alq3 reference, 2-(3”-pyridyl)-3-(N-ethyl-(3’-carbazolyl))acrylonitrile had a lightly higher value. The third harmonic generation measurement for 2-(2’-pyridyl)-3-(N-ethyl-(3’-carbazolyl))acrylonitrile yielded a χ(3) value of 5.5 × 10−12 esu, similar to that reported for commercial polymers. PMID:28880006

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

    Directory of Open Access Journals (Sweden)

    2008-01-01

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

  15. CYP2E1 Metabolism of Styrene Involves Allostery

    OpenAIRE

    2012-01-01

    We are the first to report allosterism during styrene oxidation by recombinant CYP2E1 and human liver microsomes. At low styrene concentrations, oxidation is inefficient because of weak binding to CYP2E1 (Ks = 830 μM). A second styrene molecule then binds CYP2E1 with higher affinity (Kss = 110 μM) and significantly improves oxidation to achieve a kcat of 6.3 nmol · min−1 · nmol CYP2E1−1. The transition between these metabolic cycles coincides with reported styrene concentrations in blood from...

  16. Styrene polymerization in three-component cationic microemulsions

    Energy Technology Data Exchange (ETDEWEB)

    Perez-Luna, V.H.; Puig, J.E. (Universidad de Guadalajara (Mexico)); Castano, V.M. (Instituto de Fisica (Mexico)); Rodriguez, B.E.; Murthy, A.K.; Kaler, E.W. (Univ. of Delaware, Newark (USA))

    1990-06-01

    The polymerization of styrene in three-component dodecyltrimethylammonium bromide (DTAB) microemulsions is reported. The structure of the unpolymerized microemulsions, determined by conductimetry and quasielastic light scattering (QLS), is consistent with styrene-swollen micelles in equilibrium with regular micelles, both dispersed in an aqueous phase. Polymerization of these transparent microemulsions, monitored by QLS an dilatometry, produced stable, bluish monodisperse microlatices with particle radii ranging from 20 to 30 nm, depending on styrene content. Polymerization initiation appears to occur in the styrene-swollen micelles, and the polymer particles grow by recruiting monomer and surfactant from uninitiated droplets and small micelles.

  17. Synthesis of Poly(styrene-b-isoprene-b-styrene) via Nitroxide-mediated Radical Polymerization by a Novel Alkoxyamine

    Institute of Scientific and Technical Information of China (English)

    GAO Long-cheng; PAN Qi-wei; FAN Xing-he; CHEN Xiao-fang; WAN Xin-hua; ZHOU Qi-feng

    2005-01-01

    Bifunctional alkoxyamine bis-TIPNO derived from 2,2,5-trimethyl-4-phenyl-3-azahexane-3-oxyl(TIPNO) and α, ω-alkyl bromide by atom transfer radical addition(ATRA) was employed as "biradical initiator" for nitroxide-mediated radical polymerization(NMRP) of isoprene and styrene. The kinetics study for the polymerization of styrene at different time showed living features. The poly(styrene-b-isoprene-b-styrene)(SIS) copolymers have two glass transition temperatures, indicating the immiscibility of the corresponding blocks.

  18. Scintillation of thin tetraphenyl butadiene films under alpha particle excitation

    Energy Technology Data Exchange (ETDEWEB)

    Pollmann, Tina, E-mail: tina@owl.phy.queensu.c [Department of Physics, Engineering Physics, and Astronomy, Queens University, Kingston, Ontario, K7L 3N6 (Canada); Boulay, Mark; Kuzniak, Marcin [Department of Physics, Engineering Physics, and Astronomy, Queens University, Kingston, Ontario, K7L 3N6 (Canada)

    2011-04-11

    The alpha induced scintillation of the wavelength shifter 1,1,4,4-tetraphenyl-1,3-butadiene (TPB) was studied to improve the understanding of possible surface alpha backgrounds in the DEAP dark matter search experiment. We found that vacuum deposited thin TPB films emit 882{+-}210 photons per MeV under alpha particle excitation. The scintillation pulse shape consists of a double exponential decay with lifetimes of 11{+-}5 and 275{+-}10ns.

  19. Conversion of 2,3-butanediol to butadiene

    Energy Technology Data Exchange (ETDEWEB)

    Lilga, Michael A.; Frye, Jr, John G.; Lee, Suh-Jane; Albrecht, Karl O.

    2016-09-06

    A composition comprising 2,3-butanediol is dehydrated to methyl vinyl carbinol and/or 1,3-butadiene by exposure to a catalyst comprising (a) M.sub.xO.sub.y wherein M is a rare earth metal, a group IIIA metal, Zr, or a combination thereof, and x and y are based upon an oxidation state of M, or (b) M.sup.3.sub.a(PO.sub.4).sub.b where M.sup.3 is a group IA, a group IIA metal, a group IIIA metal, or a combination thereof, and a and b are based upon the oxidation state of M.sup.3. Embodiments of the catalyst comprising M.sub.xO.sub.y may further include M.sup.2, wherein M.sup.2 is a rare earth metal, a group IIA metal, Zr, Al, or a combination thereof. In some embodiments, 2,3-butanediol is dehydrated to methyl vinyl carbinol and/or 1,3-butadiene by a catalyst comprising M.sub.xO.sub.y, and the methyl vinyl carbinol is subsequently dehydrated to 1,3-butadiene by exposure to a solid acid catalyst.

  20. COPOLYMER BLENDS OF STYRENE AND ORTHO-FLUOROSTYRENE

    NARCIS (Netherlands)

    TENBRINKE, G; KARASZ, FE

    1991-01-01

    The traditional method, using differential scanning calorimetry, to study phase behaviour in blends containing styrene and fluorinated styrene is hampered by the fact that the glass transition temperatures of fluorinated polystyrenes are almost independent of the degree of fluorination. To deal with

  1. 21 CFR 177.1810 - Styrene block polymers.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Styrene block polymers. 177.1810 Section 177.1810... FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1810 Styrene block polymers. The...

  2. 40 CFR 721.10151 - Modified styrene, divinylbenzene polymer (generic).

    Science.gov (United States)

    2010-07-01

    ... polymer (generic). 721.10151 Section 721.10151 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.10151 Modified styrene, divinylbenzene polymer (generic). (a) Chemical... as modified styrene, divinylbenzene polymer (PMN P-07-642) is subject to reporting under this section...

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

    CERN Document Server

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

    2012-01-01

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

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

    Science.gov (United States)

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

    2009-12-15

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

  5. Selective Vulnerability of the Cochlear Basal Turn to Acrylonitrile and Noise

    Directory of Open Access Journals (Sweden)

    B. Pouyatos

    2009-01-01

    Full Text Available Exposure to acrylonitrile, a high-production industrial chemical, can promote noise-induced hearing loss (NIHL in the rat even though this agent does not itself produce permanent hearing loss. The mechanism by which acrylonitrile promotes NIHL includes oxidative stress as antioxidant drugs can partially protect the cochlea from acrylonitrile+noise. Acrylonitrile depletes glutathione levels while noise can increase the formation of reactive oxygen species. It was previously noted that the high-frequency or basal turn of the cochlea was particularly vulnerable to the combined effects of acrylonitrile and noise when the octave band noise (OBN was centered at 8 kHz. Normally, such a noise would be expected to yield damage at a more apical region of the cochlea. The present study was designed to determine whether the basal cochlea is selectively sensitive to acrylonitrile or whether, by adjusting the frequency of the noise band, it would be possible to control the region of the auditory impairment. Rats were exposed to one of three different OBNs centered at different frequencies (4 kHz, 110 dB and 8 or 16 kHz at 97 dB for 5 days, with and without administration of acrylonitrile (50 mg/kg/day. The noise was set to cause limited NIHL by itself. Auditory function was monitored by recording distortion products, by compound action potentials, and by performing cochlear histology. While the ACN-only and noise-only exposures induced no or little permanent auditory loss, the three exposures to acrylonitrile+noise produced similar auditory and cochlear impairments above 16 kHz, despite the fact that the noise exposures covered 2 octaves. These observations show that the basal cochlea is much more sensitive to acrylonitrile+noise than the apical partition. They provide an initial basis for distinguishing the pattern of cochlear injury that results from noise exposure from that which occurs due to the combined effects of noise and a chemical

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

    Science.gov (United States)

    Page, N P; Cook, B

    1990-12-15

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

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

    Institute of Scientific and Technical Information of China (English)

    SHI Minxian; HUANG Zhixiong; LI Yaming; YANG Guorui

    2009-01-01

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

  8. Biofiltration of a styrene/acetone vapor mixture in two reactor types under conditions of styrene overloading

    Directory of Open Access Journals (Sweden)

    Lubos Zapotocky

    2014-10-01

    Full Text Available This aim of study was to compare the performance of a biofilter (BF and trickle bed reactor (TBR under increased styrene loading with a constant acetone load, 2 gc/m3/h. At styrene loading rates up to 30 gc/m3/h, the BF showed higher styrene removal than TBR. However, the BF efficiency started to drop beyond this threshold loading and could never reach steady state, whereas the TBR continued to yield a 50% styrene removal. The acetone removal remained constant (93-98% in both the reactors at any styrene loading. Once the overloading was lifted, the BF recovered within 26 min, whereas the TBR efficiency bounced back only to 95%, gradually returning to complete removal only in 10 h.

  9. Biocompatibility and characterization of polylactic acid/styrene-ethylene-butylene-styrene composites.

    Science.gov (United States)

    Tsou, Chi-Hui; Kao, Bo-Jyue; Yang, Ming-Chien; Suen, Maw-Cherng; Lee, Yi-Hsuan; Chen, Jui-Chin; Yao, Wei-Hua; Lin, Shang-Ming; Tsou, Chih-Yuan; Huang, Shu-Hsien; De Guzman, Manuel; Hung, Wei-Song

    2015-01-01

    Polylactic acid (PLA)/styrene-ethylene-butylene-styrene (SEBS) composites were prepared by melt blending. Differential scanning calorimetry (DSC) and wide angle X-ray diffraction (WXRD) were used to characterize PLA and PLA/SEBS composites in terms of their melting behavior and crystallization. Curves from thermal gravimetric analysis (TGA) illustrated that thermostability increased with SEBS content. Further morphological analysis of PLA/SEBS composites revealed that SEBS molecules were not miscible with PLA molecules in PLA/SEBS composites. The tensile testing for PLA and PLA/SEBS composites showed that the elongation at the break was enhanced, but tensile strength decreased with increasing SEBS content. L929 fibroblast cells were chosen to assess the cytocompatibility; the cell growth of PLA was found to decrease with increasing SEBS content. This study proposes possible reasons for these properties of PLA/SEBS composites.

  10. Sulfonated Styrene-(ethylene-co-butylene-styrene/Montmorillonite Clay Nanocomposites: Synthesis, Morphology, and Properties

    Directory of Open Access Journals (Sweden)

    Ganguly Anirban

    2007-01-01

    Full Text Available AbstractSulfonated styrene-(ethylene-butylene-styrene triblock copolymer (SSEBS was synthesized by reaction of acetyl sulfate with SEBS. SSESB-clay nanocomposites were then prepared from hydrophilic Na-montmorillonite (MT and organically (quaternary amine modified hydrophobic nanoclay (OMT at very low loading. SEBS did not show improvement in properties with MT-based nanocomposites. On sulfonation (3 and 6 weight% of SEBS, hydrophilic MT clay-based nanocomposites exhibited better mechanical, dynamic mechanical, and thermal properties, and also controlled water–methanol mixture uptake and permeation and AC resistance. Microstructure determined by X-ray diffraction, atomic force microscopy, and transmission electron microscopy due to better dispersion of MT nanoclay particles and interaction of MT with SSEBS matrix was responsible for this effect. The resulting nanocomposites have potential as proton transfer membranes for Fuel Cell applications.

  11. Metabolism and toxicity of styrene in microsomal epoxide hydrolase-deficient mice.

    Science.gov (United States)

    Carlson, Gary P

    2010-01-01

    Styrene, which is widely used in manufacturing, is both acutely and chronically toxic to mice. Styrene is metabolized by cytochromes P-450 to the toxic metabolite styrene oxide, which is detoxified via hydrolysis with microsomal epoxide hydrolase (mEH) playing a major role. The purpose of these studies was to characterize the importance of this pathway by determining the hepatotoxicity and pneumotoxicity of styrene in wild-type and mEH-deficient (mEH(-/-)) mice. While the mEH(-/-) mice metabolized styrene to styrene oxide at the same rate as the wild-type mice, as expected there was minimal metabolism of styrene oxide to glycol. mEH(-/-) mice were more susceptible to the lethal effects of styrene. Twenty-four hours following the administration of 200 mg/kg ip styrene, mice demonstrated a greater hepatotoxic response due to styrene, as measured by increased serum sorbitol dehydrogenase activity and greater pneumotoxicity as shown by increased protein levels, cell numbers, and lactate dehydrogenase activity in bronchioalveolar lavage fluid. mEH(-/-) mice were also more susceptible to styrene-induced oxidative stress, as indicated by greater decreases in hepatic glutathione levels 3 h after styrene. Styrene oxide at a dose of 150 mg/kg did not produce hepatotoxicity in either wild-type or mEH(-/-) mice. However, styrene oxide produced pneumotoxicity that was similar in the two strains. Thus, mEH plays an important role in the detoxification of styrene but not for exogenously administered styrene oxide.

  12. Neuropharmacological and cochleotoxic effects of styrene. Consequences on noise exposures.

    Science.gov (United States)

    Campo, Pierre; Venet, Thomas; Thomas, Aurélie; Cour, Chantal; Brochard, Céline; Cosnier, Frédéric

    2014-01-01

    Occupational noise exposure can damage workers' hearing, particularly when combined with exposure to cochleotoxic chemicals such as styrene. Although styrene-induced cochlear impairments only become apparent after a long incubation period, the pharmacological impact of styrene on the central nervous system (CNS) can be rapidly measured by determining the threshold of the middle-ear acoustic reflex (MER) trigger. The aim of the study was to evaluate the effects of a noise (both continuous and impulse), and a low concentration of styrene [300ppmnoise was lower (80dB SPL sound pressure level) than that of the continuous noise (85dB SPL), it appeared more detrimental to the peripheral auditory receptors. A co-exposure to styrene and continuous noise was less damaging than exposure to continuous noise alone. In contrast, the traumatic effects of impulse noise on the organ of Corti were enhanced by co-exposure to styrene. The pharmacological effects of the solvent on the CNS were discussed to put forward a plausible explanation of these surprising results. We hypothesize that CNS effects of styrene may account for this apparent paradox. Based on the present results, the temporal structure of the noise should be reintroduced as a key parameter in hearing conservation regulations.

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

    Science.gov (United States)

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

    2012-01-01

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

  14. CYP2E1 Metabolism of Styrene Involves Allostery

    Science.gov (United States)

    Hartman, Jessica H.; Boysen, Gunnar

    2012-01-01

    We are the first to report allosterism during styrene oxidation by recombinant CYP2E1 and human liver microsomes. At low styrene concentrations, oxidation is inefficient because of weak binding to CYP2E1 (Ks = 830 μM). A second styrene molecule then binds CYP2E1 with higher affinity (Kss = 110 μM) and significantly improves oxidation to achieve a kcat of 6.3 nmol · min−1 · nmol CYP2E1−1. The transition between these metabolic cycles coincides with reported styrene concentrations in blood from exposed workers; thus, this CYP2E1 mechanism may be relevant in vivo. Scaled modeling of the in vitro-positive allosteric mechanism for styrene metabolism to its in vivo clearance led to significant deviations from the traditional model based on Michaelis-Menten kinetics. Low styrene levels were notably much less toxic than generally assumed. We interrogated the allosteric mechanism using the CYP2E1-specific inhibitor and drug 4-methylpyrazole, which we have shown binds two CYP2E1 sites. From the current studies, styrene was a positive allosteric effector on 4-methylpyrazole binding, based on a 10-fold increase in 4-methylpyrazole binding affinity from Ki 0.51 to Ksi 0.043 μM. The inhibitor was a negative allosteric effector on styrene oxidation, because kcat decreased 6-fold to 0.98 nmol · min−1 · nmol CYP2E1−1. Consequently, mixtures of styrene and other molecules can induce allosteric effects on binding and metabolism by CYP2E1 and thus mitigate the efficiency of their metabolism and corresponding effects on human health. Taken together, our elucidation of mechanisms for these allosteric reactions provides a powerful tool for further investigating the complexities of CYP2E1 metabolism of drugs and pollutants. PMID:22807108

  15. Polynuclear hafnium polyhydrides with a 1,3-butadiene-1,4-diyl fragment from hydrogenolysis of a butadiene alkyl complex

    NARCIS (Netherlands)

    Visser, Cindy; Hende, Johannes R. van den; Meetsma, Auke; Hessen, Bart

    2003-01-01

    Hydrogenolysis of (eta(5)-C5Me5)Hf(2,3-dimethyl-1,3-butadiene)CH2SiMe3 leads to the formation of the mixed-valence tetranuclear polyhydride (eta(5)-C5Me5)(4)Hf-4-(sigma(1):sigma(1):eta(4):eta(4)C(6)H(8)(mu-H)(6) , with a central 2,3-dimethyl-1,3-butadiene-1,4-diyl fragment. The same reaction in the

  16. 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....

  17. Pressure dependence of the Boson peak in poly(butadiene)

    CERN Document Server

    Frick, B

    2002-01-01

    Variation of pressure and temperature in inelastic neutron scattering experiments allows us to separate density and thermal energy contributions. We summarise briefly the influence of pressure and temperature on the dynamic scattering law of the polymer glass former poly(butadiene) far below the glass transition. We also show the advantage of using a liquid-niobium pressure cell in such studies. The effect of pressure on the boson peak is to shift the peak towards higher energies and to reduce the low-frequency modes more strongly below the boson-peak maximum than above. A decrease in the Debye-Waller factor with increasing pressure is observed. (orig.)

  18. Structure and Tunneling Dynamics of gauche-1,3-BUTADIENE

    Science.gov (United States)

    Changala, Bryan; Baraban, Joshua H.; Martin-Drumel, Marie-Aline; Eibenberger, Sandra; Patterson, David; Stanton, John F.; Ellison, Barney; McCarthy, Michael C.

    2017-06-01

    We have recently shown that gauche-1,3-butadiene is unambiguously non-planar, with a C=C-C=C dihedral angle of about 34°, and readily tunnels between two equivalent gauche structures. In this talk, subsequent microwave studies of gauche-1,3-butadiene and its isotopologues as well as the empirical equilibrium structure will be summarized. The experiments have utilized the complementary techniques of cavity enhanced Fourier transform microwave (FTMW) spectroscopy with a supersonic expansion and chirped-pulse FTMW in a cryogenic buffer gas cell. The structural characterization is complicated by the effects of facile tunneling, and full dimensional ab initio rotational-VMP2 calculations have been performed to address this issue. We will show how the tunneling splitting frequency, which ranges between about 0.5 and 2.0 cm^{-1} (depending on the isotopologue), can be extracted from the experimental spectra by careful examination of tunneling-rotation perturbations. M.-A. Martin-Drumel et al., ISMS 2016, MI11

  19. Styrene-based shape memory foam: fabrication and mathematical modeling

    Science.gov (United States)

    Yao, Yongtao; Zhou, Tianyang; Qin, Chao; Liu, Yanju; Leng, Jinsong

    2016-10-01

    Shape memory polymer foam is a promising kind of structure in the biomedical and aerospace field. Shape memory styrene foam with uniform and controlled open-cell structure was successfully fabricated using a salt particulate leaching method. Shape recovery capability exists for foam programming in both high-temperature compression and low-temperature compression (Ashby as well as differential micromechanics theory were applied to predict Young’s modulus and the mechanical behavior of SMP styrene foams during the compression process.

  20. Metal and organo-catalysed asymmetric hydroaminomethylation of styrenes

    Institute of Scientific and Technical Information of China (English)

    Barbara Villa-Marcos; Jianliang Xiao

    2015-01-01

    A new protocol that enables asymmetric hydroaminomethylation of styrenes to afford chiral amines has been developed. Catalysed by an Rh‐phosphine species and a chiral phosphoric acid, styrenes are converted intoβ‐chiral amines with good enantioselectivities under syngas in the presence of an amine and Hantzsch ester. The reaction involves two key steps, hydroformylation and reductive amination, with the former catalysed by the Rh species whilst the latter by the phosphoric acid.

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

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

    WU Jinyuan; YANG Chaoxiong; WU Yuxian

    1990-01-01

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

  3. High throughput HPLC-ESI(-)-MS/MS methodology for mercapturic acid metabolites of 1,3-butadiene: Biomarkers of exposure and bioactivation.

    Science.gov (United States)

    Kotapati, Srikanth; Esades, Amanda; Matter, Brock; Le, Chap; Tretyakova, Natalia

    2015-11-05

    1,3-Butadiene (BD) is an important industrial and environmental carcinogen present in cigarette smoke, automobile exhaust, and urban air. The major urinary metabolites of BD in humans are 2-(N-acetyl-L-cystein-S-yl)-1-hydroxybut-3-ene/1-(N-acetyl-L-cystein-S-yl)-2-hydroxybut-3-ene (MHBMA), 4-(N-acetyl-L-cystein-S-yl)-1,2-dihydroxybutane (DHBMA), and 4-(N-acetyl-L-cystein-S-yl)-1,2,3-trihydroxybutyl mercapturic acid (THBMA), which are formed from the electrophilic metabolites of BD, 3,4-epoxy-1-butene (EB), hydroxymethyl vinyl ketone (HMVK), and 3,4-epoxy-1,2-diol (EBD), respectively. In the present work, a sensitive high-throughput HPLC-ESI(-)-MS/MS method was developed for simultaneous quantification of MHBMA and DHBMA in small volumes of human urine (200 μl). The method employs a 96 well Oasis HLB SPE enrichment step, followed by isotope dilution HPLC-ESI(-)-MS/MS analysis on a triple quadrupole mass spectrometer. The validated method was used to quantify MHBMA and DHBMA in urine of workers from a BD monomer and styrene-butadiene rubber production facility (40 controls and 32 occupationally exposed to BD). Urinary THBMA concentrations were also determined in the same samples. The concentrations of all three BD-mercapturic acids and the metabolic ratio (MHBMA/(MHBMA+DHBMA+THBMA)) were significantly higher in the occupationally exposed group as compared to controls and correlated with BD exposure, with each other, and with BD-hemoglobin biomarkers. This improved high throughput methodology for MHBMA and DHBMA will be useful for future epidemiological studies in smokers and occupationally exposed workers.

  4. Styrene-Associated Health Outcomes at a Windblade Manufacturing Plant

    Science.gov (United States)

    McCague, Anna-Binney; Cox-Ganser, Jean M.; Harney, Joshua M.; Alwis, K. Udeni; Blount, Benjamin C.; Cummings, Kristin J.; Edwards, Nicole; Kreiss, Kathleen

    2015-01-01

    Background Health risks of using styrene to manufacture windblades for the green energy sector are unknown. Methods Using data collected from 355 (73%) current windblade workers and regression analysis, we investigated associations between health outcomes and styrene exposure estimates derived from urinary styrene metabolites. Results The median current styrene exposure was 53.6 mg/g creatinine (interquartile range: 19.5–94.4). Color blindness in men and women (standardized morbidity ratios 2.3 and 16.6, respectively) was not associated with exposure estimates, but was the type previously reported with styrene. Visual contrast sensitivity decreased and chest tightness increased (odds ratio 2.9) with increasing current exposure. Decreases in spirometric parameters and FeNO, and increases in the odds of wheeze and asthma-like symptoms (odds ratios 1.3 and 1.2, respectively) occurred with increasing cumulative exposure. Conclusions Despite styrene exposures below the recommended 400 mg/g creatinine, visual and respiratory effects indicate the need for additional preventative measures in this industry. PMID:26305283

  5. Rapid prototyping of polymeric microstructures with a UV laser

    DEFF Research Database (Denmark)

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

    2003-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2011-07-01

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

  7. Terahertz (THz) Optical Parameters of Three-Dimensional (3-D) Printing Materials

    Science.gov (United States)

    2017-03-01

    acrylonitrile butadiene styrene (ABS), and polylactic acid (PLA). All three materials are common, low-cost, 3-D printed materials. Pictures of... Lewis , R. A., “3D Printed Terahertz Diffraction Gratings and Lenses,” Journal of Infrared Millimeter and Terahertz Waves, Volume 36, pp. 72-80...Impact polystyrene mm millimeters ns nanosecond PLA polylactic acid pp p-polarized R Reflection ss s-polarized T Transmission THz

  8. Proceedings of the Japan - U.S. Conference on Composite Materials (6th) Held in Orlando, Florida on June 22-24, 1992

    Science.gov (United States)

    1993-03-01

    and phenolic resin(FE), polyethylene terephthalate ( PET ) were studied as listed in Table 1. Among various plastics, PET and PBT were selected, then...damping value of Tabie I Samples of plastics Symbol Name ABS Acrylonitrile/butadiene/styrene PC Polycarbonate FE Phenol resin PE Polyethylene PET Poly...Poly(vinyl chloride) PBT Poly(butylene terephthalate ) HDPE High density polyethylene Table 2 Samples of FRP PET /glass fiber(O-50vol%) PBT/glass fiber(O

  9. 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.

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

    OpenAIRE

    Mohammad Shakerkhatibi; Mohammad Mosaferi; Khaled Zorufchi Benis; Zahra Akbari

    2016-01-01

    Background: The measurement data regarding the influent and effluent of wastewater treatment plant (WWTP) provides a general overview, demonstrating an overall performance of WWTP. Nevertheless, these data do not provide the suitable operational information for the optimization of individual units involved in a WWTP. A full-scale evolution of WWTP was carried out in this study via a reconciled data. Methods: A full-scale evolution of acrylonitrile, butadiene and styrene (ABS) r...

  11. Microwave Study of Recycled ABS Resins

    Institute of Scientific and Technical Information of China (English)

    A; M; Hasna

    2002-01-01

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

  12. WATER RESISTANCE OF WOOD - PLASTIC COMPOSITES MADE FROM WASTE MATERIALS RESULTED IN THE FURNITURE MANUFACTURING PROCESS

    OpenAIRE

    Camelia COŞEREANU; Dumitru LICA; Ioan CURTU; Mariana-Domnica STANCIU

    2014-01-01

    The purpose of this paper is to present innovative wood-plastic composites made from waste materials such as ABS (acrylonitrile butadiene styrene) and wood shavings resulted in the furniture manufacturing process. From previous investigations (with regard to physical integrity and compactness of the panels), only mixtures ranging from a ratio of 100% ABS: 0% shavings to 80% ABS: 20% shavings were selected for water resistance testing. Swelling in thickness and water absorption for...

  13. Glutathione transferases and glutathionylated hemoglobin in workers exposed to low doses of 1,3-butadiene.

    Science.gov (United States)

    Primavera, Alessandra; Fustinoni, Silvia; Biroccio, Antonino; Ballerini, Sabrina; Urbani, Andrea; Bernardini, Sergio; Federici, Giorgio; Capucci, Enrico; Manno, Maurizio; Lo Bello, Mario

    2008-11-01

    We evaluated glutathione transferase (GST) activities and the levels of glutathionylated hemoglobin in the RBC of 42 workers exposed to 1,3-butadiene in a petrochemical plant, using 43 workers not exposed to 1,3-butadiene and 82 foresters as internal and external controls, respectively. Median 1,3-butadiene exposure levels were 1.5, 0.4, and 0.1 microg/m3 in 1,3-butadiene-exposed workers, in workers not directly exposed to 1,3-butadiene, and in foresters, respectively. In addition, we determined in the peripheral blood lymphocytes of the same individuals the presence of GST polymorphic genes GSTT1 and GSTM1 and the distribution of GSTP1 allelic variants. Comparing the mean values observed in petrochemical workers with those of control foresters, we found a marked decrease of GST enzymatic activity and a significant increase of glutathionylated hemoglobin in the petrochemical workers. A weak but significant negative correlation was found between levels of 1,3-butadiene exposure and GST activity, whereas a positive correlation was found between 1,3-butadiene exposure and glutathionylated hemoglobin. A negative correlation was also observed between GST activity and glutathionylated hemoglobin. No influence of confounders was observed. Using a multiple linear regression model, up to 50.6% and 41.9% of the variability observed in glutathionylated hemoglobin and GST activity, respectively, were explained by 1,3-butadiene exposure, working setting, and GSTT1 genotype. These results indicate that occupational exposure to 1,3-butadiene induces an oxidative stress that impairs the GST balance in RBC, and suggest that GST activity and glutathionylated hemoglobin could be recommended as promising biomarkers of effect in petrochemical workers.

  14. Thermo Stability of Highly Sulfonated Poly(Styrene-Isobutylene-Styrene) Block Copolymers: Effects of Sulfonation and Counter-Ion Substitution

    Science.gov (United States)

    2008-01-01

    poly(styrene-isobutylene- styrene) (SIBS) tri-block co-polymer (2, 3). The major component of the tri-block co-polymer is polyisobutylene ( PIB ...which comprises 70% by weight of the base polymer. The PIB gives the material low temperature flexibility as well as excellent barrier properties. The... PIB matrix (4). The fraction of PS controls the resultant morphology, which can be for example cylinders, lamellae, spheres, or a complex mixture

  15. Optimization of injection molding parameters for poly(styrene-isobutylene-styrene) block copolymer

    Science.gov (United States)

    Fittipaldi, Mauro; Garcia, Carla; Rodriguez, Luis A.; Grace, Landon R.

    2016-03-01

    Poly(styrene-isobutylene-styrene) (SIBS) is a widely used thermoplastic elastomer in bioimplantable devices due to its inherent stability in vivo. However, the properties of the material are highly dependent on the fabrication conditions, molecular weight, and styrene content. An optimization method for injection molding is herein proposed which can be applied to varying SIBS formulations in order to maximize ultimate tensile strength, which is critical to certain load-bearing implantable applications. The number of injection molded samples required to ascertain the optimum conditions for maximum ultimate tensile strength is limited in order to minimize experimental time and effort. Injection molding parameters including nozzle temperature (three levels: 218, 246, and 274 °C), mold temperature (three levels: 50, 85, and 120 °C), injection speed (three levels: slow, medium and fast) and holding pressure time (three levels: 2, 6, and 10 seconds) were varied to fabricate dumbbell specimens for tensile testing. A three-level L9 Taguchi method utilizing orthogonal arrays was used in order to rank the importance of the different injection molding parameters and to find an optimal parameter setting to maximize the ultimate tensile strength of the thermoplastic elastomer. Based on the Taguchi design results, a Response Surface Methodology (RSM) was applied in order to build a model to predict the tensile strength of the material at different injection parameters. Finally, the model was optimized to find the injection molding parameters providing maximum ultimate tensile strength. Subsequently, the theoretically-optimum injection molding parameters were used to fabricate additional dumbbell specimens. The experimentally-determined ultimate tensile strength of these samples was found to be in close agreement (1.2%) with the theoretical results, successfully demonstrating the suitability of the Taguchi Method and RSM for optimizing injection molding parameters of SIBS.

  16. Metabolism of styrene to styrene oxide and vinylphenols in cytochrome P450 2F2- and P450 2E1-knockout mouse liver and lung microsomes.

    Science.gov (United States)

    Shen, Shuijie; Li, Lei; Ding, Xinxin; Zheng, Jiang

    2014-01-21

    Pulmonary toxicity of styrene is initiated by cytochromes P450-dependent metabolic activation. P450 2E1 and P450 2F2 are considered to be two main cytochrome P450 enzymes responsible for styrene metabolism in mice. The objective of the current study was to determine the correlation between the formation of styrene metabolites (i.e., styrene oxide and 4-vinylphenol) and pulmonary toxicity of styrene, using Cyp2e1- and Cyp2f2-null mouse models. A dramatic decrease in the formation of styrene glycol and 4-vinylphenol was found in Cyp2f2-null mouse lung microsomes relative to that in the wild-type mouse lung microsomes; however, no significant difference in the production of the styrene metabolites was observed between lung microsomes obtained from Cyp2e1-null and the wild-type mice. The knockout and wild-type mice were treated with styrene (6.0 mmol/kg, ip), and cell counts and LDH activity in bronchoalveolar lavage fluids were monitored to evaluate the pulmonary toxicity induced by styrene. Cyp2e1-null mice displayed a susceptibility to lung toxicity of styrene similar to that of the wild-type animals; however, Cyp2f2-null mice were resistant to styrene-induced pulmonary toxicity. In conclusion, both P450 2E1 and P450 2F2 are responsible for the metabolic activation of styrene. The latter enzyme plays an important role in styrene-induced pulmonary toxicity. Both styrene oxide and 4-vinylphenol are suggested to participate in the development of lung injury induced by styrene.

  17. MODELING STYRENE HYDROGENATION KINETICS USING PALLADIUM CATALYSTS

    Directory of Open Access Journals (Sweden)

    G. T. Justino

    Full Text Available Abstract The high octane number of pyrolysis gasoline (PYGAS explains its insertion in the gasoline pool. However, its use is troublesome due to the presence of gum-forming chemicals which, in turn, can be removed via hydrogenation. The use of Langmuir-Hinshelwood kinetic models was evaluated for hydrogenation of styrene, a typical gum monomer, using Pd/9%Nb2O5-Al2O3 as catalyst. Kinetic models accounting for hydrogen dissociative and non-dissociative adsorption were considered. The availability of one or two kinds of catalytic sites was analyzed. Experiments were carried out in a semi-batch reactor at constant temperature and pressure in the absence of transport limitations. The conditions used in each experiment varied between 16 - 56 bar and 60 - 100 ºC for pressure and temperature, respectively. The kinetic models were evaluated using MATLAB and EMSO software. Models using adsorption of hydrogen and organic molecules on the same type of site fitted the data best.

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

    Science.gov (United States)

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

    1977-01-01

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

  19. [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

    2017-06-27

    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.

  20. Response of Primary Human Bone Marrow Mesenchymal Stromal Cells and Dermal Keratinocytes to Thermal Printer Materials In Vitro.

    Science.gov (United States)

    Schmelzer, Eva; Over, Patrick; Gridelli, Bruno; Gerlach, Jörg C

    Advancement in thermal three-dimensional printing techniques has greatly increased the possible applications of various materials in medical applications and tissue engineering. Yet, potential toxic effects on primary human cells have been rarely investigated. Therefore, we compared four materials commonly used in thermal printing for bioengineering, namely thermally printed acrylonitrile butadiene styrene, MED610, polycarbonate, and polylactic acid, and investigated their effects on primary human adult skin epidermal keratinocytes and bone marrow mesenchymal stromal cells (BM-MSCs) in vitro. We investigated indirect effects on both cell types caused by potential liberation of soluble substances from the materials, and also analyzed BM-MSCs in direct contact with the materials. We found that even in culture without direct contact with the materials, the culture with MED610 (and to a lesser extent acrylonitrile butadiene styrene) significantly affected keratinocytes, reducing cell numbers and proliferation marker Ki67 expression, and increasing glucose consumption, lactate secretion, and expression of differentiation-associated genes. BM-MSCs had decreased metabolic activity, and exhibited increased cell death in direct culture on the materials. MED610 and acrylonitrile butadiene styrene induced the strongest expression of genes associated to differentiation and estrogen receptor activation. In conclusion, we found strong cell-type-specific effects of the materials, suggesting that materials for applications in regenerative medicine should be carefully selected not only based on their mechanical properties but also based on their cell-type-specific biological effects.

  1. Photodegradation Mechanisms of Tetraphenyl Butadiene Coatings for Liquid Argon Detectors

    CERN Document Server

    Jones, B J P; Conrad, J M; Pla-Dalmau, A

    2013-01-01

    We report on studies of degradation mechanisms of tetraphenyl butadiene (TPB) coatings of the type used in neutrino and dark matter liquid argon experiments. Using gas chromatography coupled to mass spectrometry we have detected the ultraviolet-blocking impurity benzophenone (BP). We monitored the drop in performance and increase of benzophenone concentration in TPB plates with exposure to ultraviolet (UV) light, and demonstrate the correlation between these two variables. Based on the presence and initially exponential increase in the concentration of benzophenone observed, we propose that TPB degradation is a free radical-mediated photooxidation reaction, which is subsequently confirmed by displaying delayed degradation using a free radical inhibitor. Finally we show that the performance of wavelength-shifting coatings of the type envisioned for the LBNE experiment can be improved by 10-20%, with significantly delayed UV degradation, by using a 20% admixture of 4-tert-Butylcatechol.

  2. A Study of the Fluorescence Response of Tetraphenyl-butadiene

    CERN Document Server

    Jerry, R; Bugel, L; Conrad, J M

    2010-01-01

    Tetraphenyl-butadiene (TPB) is a widely used fluorescent wavelength-shifter. A common application is in liquid-argon-based particle detectors, where scintillation light is produced in the UV at 128 nm. In liquid argon experiments, TPB is often employed to shift the scintillation light to the visible range in order to allow detection via standard photomultiplier tubes. This paper presents studies on the stability of TPB with time under exposure to light. We also examine batch-to-batch variations. We compare scintillation-grade TPB to 99% pure TPB response. In the 99% pure samples, we report a yellowing effect, and full degradation of the TPB emission-peak, upon extended exposure to light.

  3. Styrene-Isoprene-Styrene Triblock Copolymer (SIS)/Polydiphenylamine Blends for Actuator Application

    Science.gov (United States)

    Thongsak, Kraipop; Sirivat, Anuvat

    2008-03-01

    Styrene-Isoprene-Styrene triblock copolymer (SIS) is a dielectric material exhibiting many properties similar to polyisoprene elastomer, which has been widely studied for eletroactive applications. In our work, SIS films were prepared via film casting at various polystyrene (PS) contents (19 wt %, 29 wt %, and 44 wt %), yielding three different morphology films as characterized by an optical microscope, SEM, and TEM. Polydiphenylamine (PDPA), a conductive polymer, was synthesized by the oxidative polymerization and doped with HCl. For electroactive applications, electrorheological properties of pure SIS films and SIS/PDPA blends under stretching at a fixed temperature of 25^oC were measured to determine the effects of morphology (spherical, cylindrical, and lamella morphology), particle concentration, and doping level on the electrorheological properties measured: the storage and the loss modulii (G' and G''), the storage modulus responses (δG'2kV/mm), and the storage modulus sensitivities (δG'2kV/mm/G'0), under applied electric field strength varying from 0 to 2 kV/mm.

  4. Spectrophotometric study of the interaction of methylene blue with poly(styrene-co-sodium styrene sulfonate

    Directory of Open Access Journals (Sweden)

    Souha Ben Mahmoud

    2016-05-01

    Full Text Available The interaction of the cationic phenothiazine dye, the Methylene Blue (MB with poly-(sodium styrene sulfonatef–co-(styrene1-f, (PSSNa f, has been investigated by spectrophotometric method. The polyelectrolyte induced metachromasy resulting in a blue shift of the absorption maxima of the dye, in agreement with the formation of dye H-aggregates. The stability of the PSSNa-MB complexes was studied as a function of polyelectrolyte chain length, polyelectrolyte electrostatic charge density f, polyelectrolyte concentration, NaCl salt addition, tetrahydrofurane (THF addition and THF treatment. The stoichiometry of PSSNa-MB complex evaluated by the molar ratio method was found 4:1 for the fully charged PSSNa f = 1. Reversal of metachromasy was observed upon salt and THF addition, while THF treatment does not affect the complex and allows recovering the initial complex. Finally, thermodynamic parameters of the interaction between the polyelectrolyte and the dye at different temperatures, namely free energy DG, the enthalpy DH and the entropy DS have been evaluated to determine the binding constant and as a consequence the stability of the complex. The metachromasy effect was found to be more high as the chemical charge f increases and reaches its maximum value f = 1, when operating at optimal conditions. So, the PSSNa f = 1-MB complex is the most stable in comparison to the others based on lower charge density PSSNa f.

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

    Institute of Scientific and Technical Information of China (English)

    朱伟军; 屠兴超; 冯惠; 屠蔓苏; 姜波; 吴飞跃; 屠树江

    2012-01-01

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

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

    OpenAIRE

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

    1997-01-01

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

  7. (η(4)-Butadiene)Sn(0) Complexes: A New Approach for Zero-Valent p-Block Elements Utilizing a Butadiene as a 4π-Electron Donor.

    Science.gov (United States)

    Kuwabara, Takuya; Nakada, Marisa; Hamada, Jumpei; Guo, Jing Dong; Nagase, Shigeru; Saito, Masaichi

    2016-09-07

    Research on zero-valent p-block elements is a recent hot topic in synthetic and theoretical chemistry because of their novel electronic states having two lone pairs in both the s- and p-orbitals. It is considered that σ-donating ligands bearing large substituents are essential to stabilize these species. Herein, we propose a new approach using butadiene as a 4π-electron donor to stabilize zero-valent group 14 elements. During our study to explore the coordination chemistry of stannacyclopentadienyl ligands, unexpected products, in which the tin atom is coordinated by a butadiene in a η(4)-fashion, were obtained. Because butadiene is a neutral 4π-electron donating ligand, the formal oxidation number of the tin atoms of the products should be zero, which is supported by X-ray diffraction analysis and theoretical calculations. A mechanism for the formation of the products is also described.

  8. Influence of Cyclodextrin on the Styrene Polymerization

    Institute of Scientific and Technical Information of China (English)

    HU Jie; LIU Bai-ling

    2004-01-01

    Cyclodextrin (CD) are oligosaccharides consisting of 6( α ), 7( β ), 8( γ ) units of1,4-linked glucose. Due to their polar hydrophilic outer shell and relatively hydrophobic cavity, theyare able to build up host-guest complexes by inclusion of suitable hydrophobic molecules. Theformation of these complexes leads to significant changes of the solubility and reactivity of the guestmolecules, but without any chemical modification. Thus, water insoluble molecules may becomecompletely water soluble simply by mixing with an aqueous solution of native CD or CD-derivatives.Hydrogen bonds or hydrophobic interactions are responsible for the stability of the complexes and itturned out that the complexed monomers could be successfully polymerized by free radicalpolymerization in water.In our present work, using styrene as monomer, potassium peroxodisulfate as radical initiator thatreacted in water in the presence ofβ-CD but without any additional surfactant, the effect ofcyclodextrin on the polymerization was described. Additionally, the acceleration mechanism ofcyclodextrin in the polymerization was also explained based on dynamic study.Table 1 Effect of CD on the monomer reactivityIt is found that β -CD could greatly accelerate the polymerization, enhance the final conversion ofmonomer. And the more the amount of β-CD was introduced, the faster the polymerization wasobtained. From Figure 1, after 5 hours reaction at 80℃, the monomer conversion in the presence of1.0g cyclodextrin reached to 95%. However, that in absence of cyclodextrin was only 60%. And themonomer conversion was not to exceed 75% even reacted for 8 hours when no CD in reactionsystem.In order to describe the acceleration of CD in the polymerization quantitatively, based onCD and without CD. As shown in Table 1, CD produced significant effect on the monomer reactivity.The relative relativities of monomer were greatly increased with the increase of the amount of CD.

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

    Institute of Scientific and Technical Information of China (English)

    刘俊杰; 张立群; 刘力; 高富强; 肖大玲; 卢咏来

    2009-01-01

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

  10. Styrene removal from wate gas by the fungus Exophiala Jeanselmei in a biofilter

    NARCIS (Netherlands)

    Cox, Hubertus Henricus Jacobus

    1995-01-01

    Styrene is an environmental pollutant, emitted in large quantities to the atmosphere by various industrial sectors. Legislation requires industry to reduce the emission of styrene. One option to purify industrial waste gases is biological treatment in biofilters. ... Zie: Summary

  11. Styrene removal from wate gas by the fungus Exophiala Jeanselmei in a biofilter

    NARCIS (Netherlands)

    Cox, Hubertus Henricus Jacobus

    1995-01-01

    Styrene is an environmental pollutant, emitted in large quantities to the atmosphere by various industrial sectors. Legislation requires industry to reduce the emission of styrene. One option to purify industrial waste gases is biological treatment in biofilters. ... Zie: Summary

  12. Styrene removal from waste gas by the fungus Exophiala jeanselmei in a biofilter

    NARCIS (Netherlands)

    Cox, H.H.J.

    1995-01-01

    Styrene is an environmental pollutant, emitted in large quantities to the atmosphere by various industrial sectors. Legislation requires industry to reduce the emission of styrene. One option to purify industrial waste gases is biological treatment in biofilters.

  13. Oxidation of Styrene with Molecular Oxygen in Supercritical CO2

    Institute of Scientific and Technical Information of China (English)

    Tao JIANG; Bu Xing HAN; Guo Ying ZHAO; Zhong Hao LI; Yan Hong CHANG; Hai Xiang GAO; Jun Chun LI

    2004-01-01

    The oxidation of styrene with molecular oxygen catalyzed by PdCl2+CuCl2 has been investigated in supercritical CO2 with a batch reactor. The oxidative system of styrene contains four components at the beginning and seven components during the reaction. The critical temperature, critical pressure, and critical density at different conversions are determined by using a high-pressure view cell. The effect of phase behavior on the conversion and selectivity were studied. Experimental results showed that the critical parameters of the reaction mixture at fixed initial molar ratio changed with the conversion of reactant. The conversion of styrene reached maximum near the critical density of the reaction mixture. Product selectivity also varied with density of reaction mixture and could be tuned to some degree.

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

    Indian Academy of Sciences (India)

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

    2009-03-01

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

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

    Science.gov (United States)

    Manne, J.; Jäger, W.; Tulip, J.

    2010-06-01

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

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

    Science.gov (United States)

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

    2010-09-01

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

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

    OpenAIRE

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

    2011-01-01

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

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

    Science.gov (United States)

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

    2011-02-01

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

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

    Science.gov (United States)

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

    2011-01-01

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

  20. Multi-ring Aggregate Formation in Styrene Polymers

    Institute of Scientific and Technical Information of China (English)

    何炳林; 王国昌; 叶彦春; 栗凤珍; 高传喜

    1994-01-01

    The photophysical properties of some cross-linked/linear styrene polymers are studied.Ithas been further demonstrated that the phenyl multi-ring aggregate forms not only in excited state instyrene/divinylbenzene cross-linked polymers hut also in ground state.Moreover,the similar multi-ring ag-gregate has also been observed in linear polystyrene with structural heterogeneity.These results are ex-plained in terms of "superdense structure" formed by chemical cross-linking and physical gelation,whichcharacterize the morphological heterogeneity in styrene polymers.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1979-03-01

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

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

    Science.gov (United States)

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

    2014-05-01

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

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

    Institute of Scientific and Technical Information of China (English)

    WUDE-YI; N.MATSUE; 等

    1993-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

    ZHANGWanxi; CHEJitai

    1993-01-01

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

  5. Conceptual process design of extractive distillation processes for ethylbenzene/styrene separation

    NARCIS (Netherlands)

    Jongmans, Mark; Hermens, E.; Raijmakers, M.; Maassen, J.I.W.; Schuur, Boelo; de Haan, A.B.

    2012-01-01

    In the current styrene production process the distillation of the close-boiling ethylbenzene/styrene mixture to obtain an ethylbenzene impurity level of 100 ppm in styrene accounts for 75–80% of the energy requirements. The future target is to reach a level of 1–10 ppm, which will increase the

  6. 40 CFR 721.3700 - Fatty acid, ester with styrenated phenol, ethylene oxide adduct.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Fatty acid, ester with styrenated... Significant New Uses for Specific Chemical Substances § 721.3700 Fatty acid, ester with styrenated phenol... chemical substance identified generically as fatty acid, ester with styrenated phenol, ethylene...

  7. 40 CFR 721.3800 - Formaldehyde, condensated polyoxyethylene fatty acid, ester with styrenated phenol, ethylene...

    Science.gov (United States)

    2010-07-01

    ... polyoxyethylene fatty acid, ester with styrenated phenol, ethylene oxide adduct. 721.3800 Section 721.3800... Formaldehyde, condensated polyoxyethylene fatty acid, ester with styrenated phenol, ethylene oxide adduct. (a... generically as formaldehyde, condensated polyoxyethylene fatty acid, ester with styrenated phenol,...

  8. Side chain alkylation of toluene with methanol over basic zeolites - novel production route towards styrene?

    NARCIS (Netherlands)

    Rep, M.; Rep, M.

    2002-01-01

    Styrene is an important monomer for the production of different types of (co-) polymers that are used in, e.g., toys, medical devices, food packaging, paper coatings etc. Styrene is produced with several different industrial processes. In 1998, the production of styrene monomer was approximately 21

  9. 40 CFR 721.9492 - Polymers of styrene, cyclohexyl methacrylate and substituted methacrylate.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Polymers of styrene, cyclohexyl... Significant New Uses for Specific Chemical Substances § 721.9492 Polymers of styrene, cyclohexyl methacrylate...) The chemical substances identified generically as polymers of styrene, cyclohexyl methacrylate...

  10. Side chain alkylation of toluene with methanol over basic zeolites - novel production route towards styrene?

    NARCIS (Netherlands)

    Rep, Marco

    2002-01-01

    Styrene is an important monomer for the production of different types of (co-) polymers that are used in, e.g., toys, medical devices, food packaging, paper coatings etc. Styrene is produced with several different industrial processes. In 1998, the production of styrene monomer was approximately 21

  11. 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

  12. 环氧树脂阳离子无皂苯丙乳液用于纸张的表面施胶%Application of Cationic Styrene-Acrylic Emulsion Modified by Epoxy Resin on Surface Sizing

    Institute of Scientific and Technical Information of China (English)

    王西锋; 张光华; 牛恒

    2011-01-01

    以丙烯腈改性淀粉为分散剂,苯乙烯(St)、丙烯酸丁酯(BA)、甲基丙烯酸二甲基氨基乙酯(DM)为单体,丙烯酰胺(AM)为交联单体,环氧树脂(E-44)为功能单体,过硫酸钾(K2S2O3)为引发剂,采用无皂乳液聚合技术合成了一种阳离子苯丙乳液表面施胶剂,并对文化纸进行表面施胶。最佳合成工艺是:w(DM)=3%,m(St):m(BA)=3,w(AM)=4%,w(E=44)=0.3%,w(K2S2O8)=0.5%。%The cationic surface sizing of styrene-acrylic polymers were synthesized by soap-free emulsion technology, using acrylonitrile modified starch as dispersant, dimethylaminoethyl methacrylate, styrene and butyl acrylate as monomers, acrylamide as cross-link

  13. 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.

  14. Photoreductive degradation of sulfur hexafluoride in the presence of styrene

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Sulfur hexafluoride (SF6) is known as one of the most powerful greenhouse gases in the atmosphere. Reductive photodegradation of SM6 by styrene has been studied with the purpose of developing a novel remediation for sulfur hexafluoride pollution. Effects of reaction conditions on the destruction and removal efficiency (DRE) of SF6 are examined in this study. Both initial styrene-to-SF6 ratio and initial oxygen concentration exert a significant influence on DRE. SF6 removal efficiency reaches a maximum value at the initial styrene-to-SF6 ratio of 0.2. It is found that DRE increases with oxygen concentration over the range of 0 to 0.09 mol/m3 and then decreases with increasing oxygen concentration. When water vapor is fed into the gas mixture, DRE is slightly enhanced over the whole studied time scale. The X-ray Photoelectron Spectroscopy (XPS) analysis, together with gas chromatography-mass spectrometry (GC-MS) and Fourier Transform Infrared spectroscopy (FT-IR) analysis, prove that nearly all the initial fluorine residing in the gas phase is in the form of SiF4, whereas, the initial sulfur is deposited in the form of elemental sulfur, after photodegradation. Free from toxic byproducts, photodegradation in the presence of styrene may serve as a promising technique for SF6 abatement.

  15. POLYMER-SUPPORTED RARE EARTH CATALYSTS FOR STYRENE POLYMERIZATION

    Institute of Scientific and Technical Information of China (English)

    ZHAO Jian; YANG Mujie; ZHENG Yi; SHEN Zhiquan

    1991-01-01

    The neodymium complex supported on styrene-maleic anhydride copolymer (SMA·Nd) has been prepared for the first time and found to be a highly effective catalyst for the polymerization of styrene. The SMA · Nd polymeric complex is characterized by IR and its catalytic activity, and the polymerization features have been investigated in comparison with that of the conventional Ziegler-Natta catalysts. When [Nd] = 1×10-3 mol/L, [M]=5 mol/L, Al/Nd = 170 (mol ratio ) and CCl4/Nd=50(mol ratio), the polymerization conversion of styrene gets to 51.6% in six hours, and the catalytic activity reaches 1852 gPS/gNd, which is much higher than that of conventional rare earth catalysts. The polymerization reaction has an induction period and shows some characteristics of chain polymerization. The polymerization rate is the first order with respect to the concentration of styrene monomer. Addition of FeCl3 does not suppress the polymerization.

  16. Microstructure and properties of styrene acrylate polymer cement concrete

    NARCIS (Netherlands)

    Zhao Su

    1995-01-01

    The paper systematically describes the evolution of the microstructure of a styrene acrylate polymer cement concrete in relation to its mechanical properties and durability. The results presented and discussed at the present paper involve the interaction of the polymer dispersion with portland cemen

  17. Synthesis and photooxidation of styrene copolymer bearing camphorquinone pendant groups

    Directory of Open Access Journals (Sweden)

    Branislav Husár

    2012-03-01

    Full Text Available (±-10-Methacryloyloxycamphorquinone (MCQ was synthesized from (±-10-camphorsulfonic acid either by a known seven-step synthetic route or by a novel, shorter five-step synthetic route. MCQ was copolymerized with styrene (S and the photochemical behavior of the copolymer MCQ/S was compared with that of a formerly studied copolymer of styrene with monomers containing the benzil (BZ moiety (another 1,2-dicarbonyl. Irradiation (λ > 380 nm of aerated films of styrene copolymers with monomers containing the BZ moiety leads to the insertion of two oxygen atoms between the carbonyl groups of BZ and to the formation of benzoyl peroxide (BP as pendant groups on the polymer backbone. An equivalent irradiation of MCQ/S led mainly to the insertion of only one oxygen atom between the carbonyl groups of camphorquinone (CQ and to the formation of camphoric anhydride (11 covalently bound to the polymer backbone. While the decomposition of pendant BP groups formed in irradiated films of styrene copolymers with pendant BZ groups leads to crosslinking, only small molecular-weight changes in irradiated MCQ/S were observed.

  18. Secondary organic aerosol formation from the photooxidation of isoprene, 1,3-butadiene, and 2,3-dimethyl-1,3-butadiene under high NOx conditions

    Directory of Open Access Journals (Sweden)

    D. R. Cocker III

    2011-02-01

    Full Text Available Secondary organic aerosol (SOA formation from atmospheric oxidation of isoprene has been the subject of multiple studies in recent years; however, reactions of other conjugated dienes emitted from anthropogenic sources remain poorly understood. SOA formation from the photooxidation of isoprene, isoprene-1-13C, 1,3-butadiene, and 2,3-dimethyl-1,3-butadiene is investigated for high NOx conditions. The SOA yield measured in the 1,3-butadiene/NOx/H2O2 irradiation system (0.089–0.178 was close to or slightly higher than that measured with isoprene under similar NOx conditions (0.077–0.103, suggesting that the photooxidation of 1,3-butadiene is a possible source of SOA in urban air. In contrast, a very small amount of SOA particles was produced in experiments with 2,3-dimethyl-1,3-butadiene. Off-line liquid chromatography – mass spectrometry analysis revealed oligoesters as the major SOA products observed from all dienes investigated. The oligoesters originate from the unsaturated aldehyde gas-phase diene reaction products, which undergo oligoester formation through heterogeneous oxidation under high NOx conditions. Oligoesters produced by the dehydration reaction between nitrooxypolyol and 2-methylglyceric acid monomer or its oligomer were also discovered in these experiments with isoprene as the starting diene. These oligomers are possible sources of the 2-methyltetrols found in ambient aerosol samples collected under high NOx conditions. Furthermore, in low-temperature experiments also conducted in this study, the SOA yield measured with isoprene at 278 K was 2–3 times as high as that measured at 300 K under similar concentration conditions. Although oligomerization plays an important role in SOA formation from isoprene photooxidation, the observed temperature dependence of SOA yield is largely explained by gas/particle partitioning of semi-volatile compounds.

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

    Directory of Open Access Journals (Sweden)

    Mohammad Shakerkhatibi

    2016-08-01

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

  20. Morphology-properties relationship on nanocomposite films based on poly(styrene-block-diene-block-styrene copolymers and silver nanoparticles

    Directory of Open Access Journals (Sweden)

    2011-02-01

    Full Text Available A comparative study on the self-assembled nanostructured morphology and the rheological and mechanical properties of four different triblock copolymers, based on poly(styrene-block-diene-block-styrene and poly(styrene-block-diene-block-styrene matrices, and of their respective nanocomposites with 1 wt% silver nanoparticles, is reported in this work. In order to obtain well-dispersed nanoparticles in the block copolymer matrix, dodecanethiol was used as surfactant, showing good affinity with both nanoparticles and the polystyrene phase of the matrices as predicted by the solubility parameters calculated based on Hoftyzer and Van Krevelen theory. The block copolymer with the highest PS content shows the highest tensile modulus and tensile strength, but also the smallest elongation at break. When silver nanoparticles treated with surfactant were added to the block copolymer matrices, each system studied shows higher mechanical properties due to the good dispersion and the good interface of Ag nanoparticles in the matrices. Furthermore, it has been shown that semiempirical models such as Guth and Gold equation and Halpin-Tsai model can be used to predict the tensile modulus of the analyzed nanocomposites.

  1. The acrylonitrile dimer ion: A study of its dissociation via self-catalysis, self-protonation and cyclization into the pyrimidine radical cation

    NARCIS (Netherlands)

    Ervasti, H.K.; Jobst, K.J.; Burgers, P.C.; Ruttink, P.J.A.; Terlouw, J.K.

    2007-01-01

    Large energy barriers prohibit the rearrangement of solitary acrylonitrile ions, CH2CHCN+, into their more stable hydrogen-shift isomers CH2CCNH+ or CHCH–CNH+. This prompted us to examine if these isomerizations occur by self-catalysis in acrylonitrile dimer ions. Such ions, generated by chemical

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1976-12-15

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

  3. New sulfonated polystyrene and styrene-ethylene/butylene-styrene block copolymers for applications in electrodialysis.

    Science.gov (United States)

    Müller, Franciélli; Ferreira, Carlos A; Franco, Lourdes; Puiggalí, Jordi; Alemán, Carlos; Armelin, Elaine

    2012-09-27

    In this study we prepared blends of polystyrene (PS) and high-impact polystyrene (HIPS) with poly(styrene-ethylene-butylene) (SEBS) triblock copolymer. After sulfonation, blends were used to fabricate ion-exchange membranes by solvent-casting and subsequent thermal treatment to obtain homogeneous packing densities. The morphology and structure of the blends were investigated by scanning electron microscopy, atomic force microscopy, and FTIR spectroscopy. Furthermore, the thermal transitions and stability of all the blends were characterized using calorimetric techniques and compared with those of the individual polymers. Analyses of the physical properties (i.e., ionic conductivity, ion-exchange capacity, water uptake, dimensional stability, mechanical properties, etc.) showed that the performance of the PS-containing membranes is, in general, higher than that of the HIPS containing one. Furthermore, the highest sulfonation degree was also found for the PS/SEBS membranes. The capabilities of the membranes were tested by investigating the extraction of Na(+) by electrodyalisis. Comparison of the percentage of extracted ions indicates that the incorporation of SEBS results in a significant improvement with respect to membranes made of individual polymers.

  4. 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.

  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. Genetic effects of 1,3-butadiene on the mouse testis.

    Science.gov (United States)

    Brinkworth, M H; Anderson, D; Hughes, J A; Jackson, L I; Yu, T W; Nieschlag, E

    1998-01-16

    1,3-Butadiene is a known male mouse germ-cell mutagen, to which humans may either be occupationally or environmentally exposed. Prolonged exposure to moderate or high doses in male mice can cause dominant lethal mutations and one report has indicated that 10 week inhalation administration of low doses can result in the production of malformed foetuses. The present study had dual purposes: (a) to attempt to clarify the suspected ability of sub-chronic (6 h/day, 5 days/wk, 10 weeks) low-dose exposure to 1,3-butadiene to induce heritable mutations in mouse male germ cells: (b) investigation of the relationships between testicular DNA damage, testicular DNA repair and foetal outcome. Adult male mice were exposed to low or moderate doses of 1,3-butadiene by inhalation sub-chronically or for a single 6 h period and either used for mating (sub-chronic exposure only) or for studies of DNA damage and repair. Litter size, dominant lethality and numbers of abnormal foetuses were determined the day preceding the normal day of parturition. Testicular DNA damage and repair were assessed by the Comet assay (for DNA damage) and the unscheduled DNA synthesis assay (for DNA repair). 1,3-Butadiene caused a statistically significant increase in dominant lethality at 125 ppm but not 12.5 ppm. No significant increase in DNA repair was found with either dose level or exposure period while only 6 h exposure to 125 ppm caused a small but significant increase in DNA damage as detected by the Comet assay. These effects demonstrate the reproductive genotoxicity of (125 ppm) 1,3-butadiene but do not confirm its ability to cause abnormalities in the offspring via the sperm. It is suggested that the relationship between 1,3-butadiene-induced DNA damage, DNA repair and heritable defects in the offspring may depend on the pattern of metabolites produced.

  7. Evaporative emissions of 1,3-butadiene from petrol-fuelled motor vehicles

    Science.gov (United States)

    Ye, Y.; Galbally, I. E.; Weeks, I. A.; Duffy, B. L.; Nelson, P. F.

    This study reports the identification and quantification of 1,3-butadiene in petrol and in the evaporative emissions from Australian light-duty passenger vehicles. The mass fraction of 1,3-butadiene in each of the different grades of any brand of Australian petrol was found to be relatively constant for a given marketing area. However, the mass fractions vary significantly between the different brands (or refineries) from 0.004±0.001% to 0.047±0.008%. The measurements of the evaporative emissions of 1,3-butadiene from in-service motor vehicles were performed using standard Australian Design Rule 37/00 (ADR 37/00) Sealed Housing Evaporative Determination (SHED) tests. For post-1985 catalyst equipped vehicles fuelled with unleaded petrol, average evaporative emissions of 1,3-butadiene were 9.4 (0.7-22) and 5.0 (0.1-23) mg per test for diurnal and hot soak SHED tests, respectively. The corresponding average evaporative emissions for the older, pre-1986 non-catalyst equipped vehicles fuelled with leaded petrol were 26.5 (11.7-45.4) and 9.2 (4.3-13.1) mg per test, respectively, about double the observed emissions from newer vehicles. For the complete vehicle set (all ages), the average mass fraction of 1,3-butadiene in the total hydrocarbon (sum of C 1-C 10 hydrocarbons) emission was 0.21±0.14% from the diurnal phase and was 0.11±0.06% from the hot-soak phase. Evaporative emissions were estimated to contribute about 4% (ranging from 1-15%) of the total (exhaust and evaporative) emissions of 1,3-butadiene from Australian motor vehicles.

  8. Removal of styrene from waste gas stream using a biofilter

    Directory of Open Access Journals (Sweden)

    B Bina

    2004-12-01

    Full Text Available Background: Styrene is produced in large quantities in the chemical industries and it has been listed among the 189 hazardous and toxic atmospheric contaminants under Clean Air Act Amendments, 1990, due to its adverse effects on human health. The biofiltration has been widely and efficiently applied during recent decades for the treatment of air streams contaminated by volatile organic compounds at low concentrations. Also this technology has been applied widely and efficiently in the removal of styrene from waste gas streams. Methods: Biofiltration of waste gas stream polluted by styrene vapor was investigated in a three-stage bench scale reactor. Yard waste compost using shredded hard plastics as a bulking agent in a 75:25 v/v mix of plastics:compost was used to packing biofilter. The system inoculation was achieved by adding thickened activated sludge obtained from municipal wastewater treatment plant and the effects of loading rate, inlet concentration, and empty bed retention time variations on the performance and operation of biofilter were studied. Results: Microbial acclimation to styrene was achieved with inlet concentration of 65 ± 11 ppm and bed contact time of 360 s after 57 days of operation. Under steady state conditions experimental results showed equal average removal efficiency of about 84% at loading rates of 60 and 80 g m-3 h-1 with empty bed retention time of 60 s. Maximum elimination capacity was obtained up to 81 g m-3 h-1 with organic loading rate of about 120 g m-3 h-1. Reduction in performance was observed at inlet concentrations of upper than 650 ppm related to organic loading rates up to 160 g m-3 h-1 and then removal efficiency was decreased sharply. Evaluation of the concentration profile along the bed height of column indicated that the most value of elimination capacity occurred in the first section of biofilter. Elimination capacity also showed higher performance when empty bed retention time was reduced to 30 s

  9. Sequential shape-selective adsorption and photocatalytic transformation of acrylonitrile production wastewater.

    Science.gov (United States)

    Dai, Yunrong; Song, Yonghui; Tu, Xiang; Jiang, Yanpeng; Yuan, Yu

    2015-11-15

    Acrylonitrile production wastewater has been widely recognized as one type of refractory organic wastewater because of its complicated composition and low bioavailability. It usually contains plenty of micromolecular nitrile and pyridine, resulting in high chemical oxygen demand (CODCr), total organic carbon (TOC) and total nitrogen (TN) concentrations. In this study, a novel microporous zeolite, CS-Z1, was developed as an adsorbent for rapidly shape-selective adsorption of the micromolecular pollutants from the acrylonitrile production wastewater, and a visible light-driven Ti-β-Bi2O3 photocatalysis was introduced to sequentially treat the residual macromolecular pollutants for complete purification. The adsorption processes by CS-Z1 were mostly achieved within the first 5 min, and the equilibrium was reached quickly after 30 min, where the CODCr, TOC and TN removal efficiencies of the wastewater were as high as 93.5%, 92.2% and 96.8%, respectively, much higher than those by other adsorbents. Furthermore, the adsorption efficiencies of CS-Z1 were barely affected by the variation of pH value and temperature, which was mainly attributed to the shape-selective adsorption mechanism of the CS-Z1 zeolite. The Ti-β-Bi2O3 photocatalysis could remove more than 95% of the residual macromolecular pollutants in the wastewater, where a synergistic mechanism of reduction-oxidation/polymerization was proposed. In a 108 h of CS-Z1 adsorption and Ti-β-Bi2O3 photocatalysis sequential process, the CODCr, TOC and TN concentrations was reduced to below 20, 7 and 5 mg L(-1), respectively, demonstrating the excellent practical potential of the sequential treatment system for acrylonitrile production wastewater. Copyright © 2015 Elsevier Ltd. All rights reserved.

  10. Simulation of Particle Growth in Gas Phase Polymerization of Butadiene by the Multigrain Model

    Institute of Scientific and Technical Information of China (English)

    孙建中; 赵军子; 何斯征; 周其云

    2001-01-01

    Gas phase polymerization of butadiene by neodymium catalyst was modeled. The effects of mass and heat transfer resistances in the external boundary layer and within particles, sorption of butadiene in polybutadiene,and deactivation of active sites on polymer particle growth and morphology were studied. Simulation results show that the effects of intraparticle mass and heat transfer resistances on the growth rate of polymer particles are insignificant, and that there is no significant effect of mass transfer resistance on the morphology of polymer particles.The simulation results were compared with the experimental results.

  11. Azidated Ether-Butadiene-Ether Block Copolymers as Binders for Solid Propellants

    Science.gov (United States)

    Cappello, Miriam; Lamia, Pietro; Mura, Claudio; Polacco, Giovanni; Filippi, Sara

    2016-07-01

    Polymeric binders for solid propellants are usually based on hydroxyl-terminated polybutadiene (HTPB), which does not contribute to the overall energy output. Azidic polyethers represent an interesting alternative but may have poorer mechanical properties. Polybutadiene-polyether copolymers may combine the advantages of both. Four different ether-butadiene-ether triblock copolymers were prepared and azidated starting from halogenated and/or tosylated monomers using HTPB as initiator. The presence of the butadiene block complicates the azidation step and reduces the storage stability of the azidic polymer. Nevertheless, the procedure allows modifying the binder properties by varying the type and lengths of the energetic blocks.

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

    Institute of Scientific and Technical Information of China (English)

    YANG Chaoxiong; WU Jinyuan; WU Yuxian

    1991-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

    WU Jinyuan; YANG Chaoxiong; ZHANG Guangzhao

    1993-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

    XU Kang; DENG Zhenghua; WAN Guoxiang

    1991-01-01

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

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

    Science.gov (United States)

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

    2008-04-01

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

  16. Crystallization analysis fractionation of poly(ethylene-co-styrene) produced by metallocene catalysts

    KAUST Repository

    Kamal, Muhammad Shahzad

    2013-06-06

    Ethylene homo polymer and ethylene-styrene copolymers were synthesized using Cp2ZrCl2 (1)/methyl aluminoxane (MAO) and rac-silylene-bis (indenyl) zirconium dichloride (2)/MAO catalyst systems by varying styrene concentration and reaction conditions. Crystallization analysis fractionation (CRYSTAF), DSC, FTIR and 1H NMR spectroscopy were used for characterizing the synthesized polymers. Interestingly, styrene was able to increase the activity of 1/MAO and 2/MAO catalyst systems at low concentrations, but at higher concentrations the activity decreases. The 1/MAO system at low and high pressure was unable to incorporate styrene, and the final product was pure polyethylene. On the other hand, with 2/MAO polymerization of ethylene and styrene yielded copolymer containing both styrene and ethylene. Results obtained from CRYSTAF and DSC reveal that on using 1/MAO system at high pressure, the resulting polymer in the presence of styrene has similar crystallinity as the polymer produced without styrene. Using both 1/MAO at low pressure and 2/MAO leads to decrease in crystallinity with increase in styrene concentration, even though the former does not incorporate styrene. © 2013 Springer-Verlag Berlin Heidelberg.

  17. Grafting of diethyl maleate and maleic anhydride onto styrene-b-(ethylene-co-1-butene)-b-styrene triblock copolymer (SEBS)

    NARCIS (Netherlands)

    Picchioni, F.; Ghetti, S.; Passaglia, E.; Ruggeri, G.

    2000-01-01

    In this paper a study of the bulk functionalization of styrene-b-(ethylene-co-1-butene)-b-styrene triblock copolymer (SEBS) with diethyl maleate (DEM) or maleic anhydride (MAH) and dicumyl peroxide (DCP) as initiator in a Brabender mixer is described. The determination of the functionalization degre

  18. SYNTHESIS OF STYRENIC TONER PARTICLES BY SPG EMULSIFICATION TECHNIQUE

    Institute of Scientific and Technical Information of China (English)

    Suda Kiatkamjornwong; Roongkan Nuisin; Guang-Hui Ma; Shinzo Omi

    2000-01-01

    This research studied the initiator efficiency for producing polymeric particles of poly(styrene-co-methyl methacrylate) copolymers by a Shirasu porous glass membrane (SPG) emulsification technique followed by suspension copolymerization. BPO, ADVN, and AIBN were used as initiators and we found that BPO is the most suitable initiator.Copolymers for various feed ratios of styrene/methyl methacrylate were thus synthesized by benzoyl peroxide, and their copolymer particle size, molecular weight distribution and particle size distribution were characterized. Then n-BMA or 2-EHMA was added as the third monomer to decrease the terpolymcr glass transition temperature. This article describes the preparation technique, recipes and polymerization conditions for producing both copolymer and terpolymer particles, particle size changes, the corresponding particle morphologies and glass transition temperatures.

  19. Effect of ultrasonic pretreatment on emulsion polymerization of styrene.

    Science.gov (United States)

    Nagatomo, Daichi; Horie, Takafumi; Hongo, Chizuru; Ohmura, Naoto

    2016-07-01

    This study investigated the effect of pretreatment of ultrasonic irradiation on emulsion polymerization of styrene to propose a process intensification method which gives high conversion, high reaction rate, and high energy efficiency. The solution containing styrene monomer was irradiated by a horn mounted on the ultrasonic transducer with the diameter of 5mm diameter and the frequency of 28 kHz before starting polymerization. The pretreatment of ultrasound irradiation as short as 1 min drastically improved monomer dispersion and increased reaction rate even under the agitation condition with low rotational speed of impeller. Furthermore, the ultrasonic pretreatment resulted in higher monomer concentration in polymer particles and produced larger polymer particles than conventional polymerization without ultrasonic pretreatment.

  20. Modification of isotactic polypropylene with styrene block-copolymers

    OpenAIRE

    DENAC, Matjaž; Musil, Vojko; Makarovič, Matjaž

    2015-01-01

    With a modification the current properties of polymeric material can be improved, and even some new properties can be obtained. The success of polymeric modifiers mostly depend on the interaction intensity at the phase boundary of the polymer/modifier. The influence of polymeric modifiers on polypropylene matrices were investigated. Different sorts and types of styrene block-copolymers were used in a concentration range up to 20 vol.%. Samples were prepared by melt-mixing in a Brabender knead...

  1. Electrochemical Dicarboxylation of Styrene: Synthesis of 2-Phenylsuccinic Acid

    Institute of Scientific and Technical Information of China (English)

    WANG, Huan; LIN, Mei-Yu; FANG, Hui-Jue; CHEN, Ting-Ting; LU, Jia-Xing

    2007-01-01

    Electrochemical dicarboxylation of styrene in the presence of atmospheric pressure of CO2 with a Ti cathode monium bromide to give 2-phenylsuccinic acid. Influences of the nature of the electrodes, the current density, the passed charge and the temperature on electrolysis were studied to optimize the electrolytic conditions, with the maximal isolated yield to be 86.07%. The mechanism of the elelctrocarboxylation process has been studied by cyclic voltammetry.

  2. Styrene biofiltration in a trickle-bed reactor

    Directory of Open Access Journals (Sweden)

    V. Novak

    2008-04-01

    Full Text Available The biological treatment of styrene waste gas in a trickle-bed filter (TBF was investigated. The bioreactor consisted of a two-part glass cylinder (ID 150 mm filled with 25 mm polypropylene Pall rings serving as packing material. The bed height was 1m. Although the laboratory temperature was maintained at 22 ºC, the water temperature in the trickle-bed filter was slightly lower (about 18 ºC.The main aim of our study was to observe the effect of empty-bed residence time (EBRT on bioreactor performance at a constant pollutant concentration over an extended time period. The bioreactor was inoculated with a mixed microbial consortium isolated from a styrene-degrading biofilter that had been running for the previous two years. After three weeks of acclimation period, the bioreactor was loaded with styrene (100 mg.m-3. EBRT was in the range of 53 s to 13 s. A maximum elimination capacity (EC of 11.3 gC.m-3.h-1 was reached at an organic loading (OL rate of 18.6 gC.m-3.h-1.

  3. 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)

  4. Quantitation of DNA Adducts Induced by 1,3-Butadiene

    Science.gov (United States)

    Sangaraju, Dewakar; Villalta, Peter W.; Wickramaratne, Susith; Swenberg, James; Tretyakova, Natalia

    2014-07-01

    Human exposure to 1,3-butadiene (BD) present in automobile exhaust, cigarette smoke, and forest fires is of great concern because of its potent carcinogenicity. The adverse health effects of BD are mediated by its epoxide metabolites such as 3,4-epoxy-1-butene (EB), which covalently modify genomic DNA to form promutagenic nucleobase adducts. Because of their direct role in cancer, BD-DNA adducts can be used as mechanism-based biomarkers of BD exposure. In the present work, a mass spectrometry-based methodology was developed for accurate, sensitive, and precise quantification of EB-induced N-7-(1-hydroxy-3-buten-2-yl) guanine (EB-GII) DNA adducts in vivo. In our approach, EB-GII adducts are selectively released from DNA backbone by neutral thermal hydrolysis, followed by ultrafiltration, offline HPLC purification, and isotope dilution nanoLC/ESI+-HRMS3 analysis on an Orbitrap Velos mass spectrometer. Following method validation, EB-GII lesions were quantified in human fibrosarcoma (HT1080) cells treated with micromolar concentrations of EB and in liver tissues of rats exposed to sub-ppm concentrations of BD (0.5-1.5 ppm). EB-GII concentrations increased linearly from 1.15 ± 0.23 to 10.11 ± 0.45 adducts per 106 nucleotides in HT1080 cells treated with 0.5-10 μM DEB. EB-GII concentrations in DNA of laboratory rats exposed to 0.5, 1.0, and 1.5 ppm BD were 0.17 ± 0.05, 0.33 ± 0.08, and 0.50 ± 0.04 adducts per 106 nucleotides, respectively. We also used the new method to determine the in vivo half-life of EB-GII adducts in rat liver DNA (2.20 ± 0.12 d) and to detect EB-GII in human blood DNA. To our knowledge, this is the first application of nanoLC/ESI+-HRMS3 Orbitrap methodology to quantitative analysis of DNA adducts in vivo.

  5. Sulfonate-containing Copolymers Prepared by Semi-Continuous Emulsion Copolymerizaiton of Styrene and Sodium Styrene Sulfonate

    Institute of Scientific and Technical Information of China (English)

    Shiming HUANG; Wei XIE; Chengyou KAN; Yajie LI; Deshan LIU

    2005-01-01

    @@ 1Introduction Soap-free emulsion copolymerization of styrene (St) and sodium sulfonate styrene (NaSS) could yield homodisperse sulfonate-containing particles with clean surface. But the incorporation of NaSS could never be increased beyond 2.6 % by weight in the conventional batch and seeded emulsion copolymerization in the absence of emulsifier because large amounts of soluble polyelectrolyte would unstablize the reaction system if excessive amount of NaSS was used[1]. In our work, semi-continuous copolymerizations were carried out in the presence of mixed emulsifiers, and a new method to purify the latex polymer was developed. The influences of the NaSS mole ratio in the total monomers and the monomer addition time on the S content in the purified copolymer were investigated by elemental analysis.

  6. Characterization of a Poly(styrene-block-methylacrylate-random-octadecylacrylate-block-styrene) Shape Memory ABA Triblock Copolymer

    Science.gov (United States)

    Fei, Pengzhan; Cavicchi, Kevin

    2011-03-01

    A new ABA triblock copolymer of poly(styrene-block- methylacrylate-random-octadecylacrylate-block-styrene) (PS-b- PMA-r-PODA-b-PS) was synthesized by reversible addition fragmentation chain transfer polymerization. The triblock copolymer can generate a three-dimensional, physically crosslinked network by self-assembly, where the glassy PS domains physically crosslink the midblock chains. The side chain crystallization of the polyoctadecylacrylare (PODA) side chain generates a second reversible network enabling shape memory properties. Shape memory tests by uniaxial deformation and recovery of molded dog-bone shape samples demonstrate that shape fixities above 96% and shape recoveries above 98% were obtained for extensional strains up to 300%. An outstanding advantage of this shape memory material is that it can be very easily shaped and remolded by elevating the temperature to 140circ; C, and after remolding the initial shape memory properties are totally recovered by eliminating the defects introduced by the previous deformation cycling.

  7. Stabilization of polypropylene, polypropylene blends with poly (styrene-b-(ethylene-co-butylene)-b-styrene) under irradiation: A comparative investigation

    Energy Technology Data Exchange (ETDEWEB)

    Luan Shifang; Yang Huawei; Shi Hengchong; Zhao Jie [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Wang Jianwei [Shandong Weigao Group Medical Polymer Company Limited, Weihai 264209 (China); Yin Jinghua, E-mail: yinjh@ciac.jl.c [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China)

    2011-01-15

    The aim of this paper is to investigate the stabilization of polypropylene in the poly (styrene-b-(ethylene-co-butylene)-b-styrene) (SEBS)/polypropylene (PP) blends under irradiation with respect to PP. The PP films, SEBS/PP films were subjected to electron beam irradiation and characterized by wide angle X-ray diffraction (WAXD), differential scanning calorimetry (DSC), gel permeation chromatography (GPC), and dynamic mechanical thermal analysis (DMTA). It demonstrated that upon irradiation, the molecular weight of PP had a pronounced decrease due to the major chain scission, and the minor chain cross-linking or chain branching occurred at the higher irradiation dose. Stabilization of PP was improved in the presence of SEBS, exhibiting an enhanced irradiation resistance.

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

    Institute of Scientific and Technical Information of China (English)

    LI Jun; HAN Na; ZHANG Xing-xiang

    2006-01-01

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

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

    Science.gov (United States)

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

    2012-05-01

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

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

    Science.gov (United States)

    Sun, Jingyu; Wang, Rongshun; Wang, Baoshan

    2011-10-01

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

  11. Toxicity of the styrene metabolite, phenylglyoxylic acid, in rats after three months' oral dosing

    DEFF Research Database (Denmark)

    Ladefoged, Ole; Lam, Henrik Rye; Ostergaard, G.

    1998-01-01

    of the effects on kidney, peripheral nerves, and vision, which have previously been reported after exposure to styrene, might be induced by the styrene metabolite, PGA. If PGA has ototoxic effects in rats, the dosing in the present study is not sufficient to induce the necessary ototoxic concentration in blood....... Alternatively, the ototoxicity of styrene, like toluene, may be caused the parent compound itself and not by a metabolite like PGA. (C) 1998 Inter Press, inc....

  12. Cooperative effects for CYP2E1 differ between styrene and its metabolites

    OpenAIRE

    2013-01-01

    Cooperative interactions are frequently observed in the metabolism of drugs and pollutants by cytochrome P450s; nevertheless, the molecular determinants for cooperativity remain elusive. Previously, we demonstrated that steady-state styrene metabolism by CYP2E1 exhibits positive cooperativity.We hypothesized that styrene metabolites have lower affinity than styrene toward CYP2E1 and limited ability to induce cooperative effects during metabolism. To test the hypothesis, we determined the pote...

  13. Biomonitoring of benzene and 1,3-butadiene exposure and early biological effects in traffic policemen.

    Science.gov (United States)

    Arayasiri, Manaswee; Mahidol, Chulabhorn; Navasumrit, Panida; Autrup, Herman; Ruchirawat, Mathuros

    2010-09-15

    The objective of this study was to determine benzene and 1,3-butadiene exposure through ambient air and personal air monitoring, as well as through biomarkers of exposure, and to evaluate the potential health risk of exposure through the use of biomarkers of early biological effects in central Bangkok traffic policemen. Ambient air concentrations of benzene and 1,3-butadiene at the roadsides were significantly higher than in police offices used as control sites (pbutadiene (median 3.08 microg/m(3)) than office policemen (median 6.17 microg/m(3) for benzene and 0.37 microg/m(3) for 1,3-butadiene) (pbutadiene metabolite, monohydroxy-butenyl mercapturic acid. Biomarkers of early biological effects, 8-hydroxy-2'-deoxyguanosine in leukocytes (8-OHdG), DNA-strand breaks, and DNA-repair capacity, measured as an increase in gamma ray-induced chromosome aberrations were significantly higher in traffic policemen than controls (pbutadiene exposure were significantly associated with 8-OHdG and olive tail moment at pbutadiene on DNA damage. These results indicated that traffic policemen, who are exposed to benzene and 1,3-butadiene at the roadside in central Bangkok, are potentially at a higher risk for development of diseases such as cancer than office policemen.

  14. Emission of 1,3-butadiene from petrol-driven motor vehicles

    Science.gov (United States)

    Ye, Y.; Galbally, I. E.; Weeks, I. A.

    This study reports the measurement of 1,3-butadiene emissions from 30 petrol-driven vehicles from the Australian car fleet using the Australian Design Rule 37/00 vehicle test procedure. Six of the cars tested were not equipped with catalytic converters and used leaded petrol as fuel. The remaining 24 cars were fitted with catalytic converters and used unleaded petrol. 1,3-Butadiene in exhaust samples was found to degrade rapidly in SUMMA treated stainless steel canisters and the degradation followed first-order kinetics. The rate coefficient of the decay can be represented by a linear dependence on the concentration of nitrogen oxides in the exhaust ( r2 = 0.79, n = 43), and the gas-phase reaction of NO 2 and 1,3-butadiene may have a major role in this loss. The 1,3-butadiene concentrations used to estimate vehicle emissions were corrected for this loss using the decay rate constant either observed from replicate analyses or from the NO x concentrations in the samples. The measurements showed that 1,3-butadiene was emitted at a rate of 20.7 ± 9.2 mg km -1 from 6 non-catalyst vehicles. There was considerable scatter in the observations from catalyst equipped vehicles and we infer that this was due to the malfunction of the emission control devices on some vehicles. The 19 vehicles that appeared to have functioning catalyst emission control devices had an average emission rate of 2.1 ± 1.5 mg km -1. These emission rates are consistent with atmospheric observations and are much higher than those reported previously. We calculate that more than 90% of the 1,3-butadiene in engine exhaust comes from the common alkane and aromatic constituents of the fuel. A comparison of emissions in the different phases of the drive cycle indicates that current emission controls remove more than 90% of the 1,3-butadiene from the initial exhaust mixture.

  15. Exposure and risk assessment of 1,3-butadiene in Japan.

    Science.gov (United States)

    Higashino, Haruyuki; Mita, Kazuaki; Yoshikado, Hiroshi; Iwata, Mitsuo; Nakanishi, Junko

    2007-03-20

    1,3-Butadiene is on the list of Substances Requiring Priority Action published by the Central Environmental Council of Japan in 1996. Emission of 1,3-butadiene has been controlled by a voluntary reduction program since 1997. Although the industrial emission of 1,3-butadiene in Japan has decreased in recent years, primarily due to a voluntary industrial emissions reduction program, the risks of exposure to it remain largely unknown. We assessed the risks and consequences of exposure to 1,3-butadiene on human health. A remarkable advantage of our risk assessment approach is the detailed assessment of exposure. Previously, we developed two different models that can be applied for the assessment of exposure: the first, the AIST-ADMER model estimates regional concentration distributions, whereas the second, the METI-LIS model estimates concentration distributions in the vicinity of factories. Both models were used for the assessment of exposure to 1,3-butadiene. Using exposure concentration and carcinogenic potency determined and reported by Environment Canada and Health Canada, we evaluated the excess lifetime cancer risk for persons exposed to 1,3-butadiene over the course of a lifetime. The results suggested that the majority of the population in Japan has an excess lifetime cancer risk of less than 10(-5), whereas a small number of people living close to industrial sources had a risk of greater than 10(-5). The results of the present assessment also showed that 1,3-butadiene in the general environment originates primarily from automobile emissions, such that a countermeasure of reducing emissions from cars is expected to be effective at reducing the total cancer risk among Japanese. On the other hand, individual risks among a population living in the vicinity of certain industrial sources were found to be significantly higher than those of the population living elsewhere, such that a reduction in emissions from a small number of specific industrial sources should be

  16. Cooperative effects for CYP2E1 differ between styrene and its metabolites

    Science.gov (United States)

    Hartman, Jessica H.; Boysen, Gunnar; Miller, Grover P.

    2014-01-01

    Cooperative interactions are frequently observed in the metabolism of drugs and pollutants by cytochrome P450s; nevertheless, the molecular determinants for cooperativity remain elusive. Previously, we demonstrated that steady-state styrene metabolism by CYP2E1 exhibits positive cooperativity.We hypothesized that styrene metabolites have lower affinity than styrene toward CYP2E1 and limited ability to induce cooperative effects during metabolism. To test the hypothesis, we determined the potency and mechanism of inhibition for styrene and its metabolites toward oxidation of 4-nitrophenol using CYP2E1 Supersomes® and human liver microsomes.Styrene inhibited the reaction through a mixed cooperative mechanism with high affinity for the catalytic site (67 μM) and lower affinity for the cooperative site (1100 μM), while increasing substrate turnover at high concentrations. Styrene oxide and 4-vinylphenol possessed similar affinity for CYP2E1. Styrene oxide behaved cooperatively like styrene, but 4-vinylphenol decreased turnover at high concentrations. Styrene glycol was a very poor competitive inhibitor. Among all compounds, there was a positive correlation with binding and hydrophobicity.Taken together, these findings for CYP2E1 further validate contributions of cooperative mechanisms to metabolic processes, demonstrate the role of molecular structure on those mechanisms and underscore the potential for heterotropic cooperative effects between different compounds. PMID:23327532

  17. Evaluation of long-term occupational exposure to styrene vapor on olfactory function.

    Science.gov (United States)

    Dalton, Pamela; Lees, Peter S J; Gould, Michele; Dilks, Daniel; Stefaniak, Aleksandr; Bader, Michael; Ihrig, Andreas; Triebig, Gerhard

    2007-10-01

    The primary sensory neurons of the olfactory system are chronically exposed to the ambient environment and may therefore be susceptible to damage from occupational exposure to many volatile chemicals. To investigate whether occupational exposure to styrene was associated with olfactory impairment, we examined olfactory function in 2 groups: workers in a German reinforced-plastics boat-manufacturing facility having a minimum of 2 years of styrene exposure (15-25 ppm as calculated from urinary metabolite concentrations, with historical exposures up to 85 ppm) and a group of age-matched workers from the same facility with lower styrene exposures. The results were also compared with normative data previously collected from healthy, unexposed individuals. Multiple measures of olfactory function were evaluated using a standardized battery of clinical assessments from the Monell-Jefferson Chemosensory Clinical Research Center that included tests of threshold sensitivity for phenylethyl alcohol (PEA) and odor identification ability. Thresholds for styrene were also obtained as a measure of occupational olfactory adaptation. Styrene exposure history was calculated through the use of past biological monitoring results for urinary metabolites of styrene (mandelic acid [MA], phenylglyoxylic acid [PGA]); current exposure was determined for each individual using passive air sampling for styrene and biological monitoring for styrene urinary metabolites. Current mean effective styrene exposure during the day of olfactory testing for the group of workers who worked directly with styrene resins was 18 ppm styrene (standard deviation [SD] = 14), 371 g/g creatinine MA + PGA (SD = 289) and that of the group of workers with lower exposures was 4.8 ppm (SD = 5.2), 93 g/g creatinine MA+PGA (SD = 100). Historic annual average exposures for all workers were greater by a factor of up to 6x. No differences unequivocally attributable to exposure status were observed between the Exposed and

  18. Bacterial degradation of styrene in waste gases using a peat filter

    Energy Technology Data Exchange (ETDEWEB)

    Arnold, M.; Reittu, A. [Kuopio Univ. (Finland). Dept. of Environmental Sciences; Wright, A. von; Suihko, M.L. [VTT Biotechnology and Food Research (Finland); Martikainen, P.J. [Kuopio Univ. (Finland). Dept. of Environmental Sciences]|[National Public Health Inst., Lab. of Environmental Microbiology, Kuopio (Finland)

    1997-12-31

    A biofiltration process was developed for styrene-containing off-gases using peat as filter material. The average styrene reduction ratio after 190 days of operation was 70% (max. 98%) and the mean styrene elimination capacity was 12 g m{sup -3} h{sup -1} (max. 30 g m{sup -3} h{sup -1}). Efficient styrene degradation required addition of nutrients to the peat, adjustment of the pH to a neutral level and efficient control of the humidity. Maintenance of the water balance was easier in a down-flow than in an up-flow process, the former consequently resulting in much better filtration efficiency. The optimum operation temperature was around 23 C, but the styrene removal was still satisfactory at 12 C. Seven different bacterial isolates belonging to the genera Tsukamurella, Pseudomonas, Sphingomonas, Xanthomonas and an unidentified genus in the {gamma} group of the Proteobacteria isolated from the microflora of active peat filter material were capable of styrene degradation. The isolates differed in their capacity to decompose styrene to carbon dioxide and assimilate it to biomass. No toxic intermediate degradation products of styrene were detected in the filter outlet gas or in growing cultures of isolated bacteria. The use of these isolates in industrial biofilters is beneficial at low styrene concentrations and is safe from both the environmental and public health points of view. (orig.)

  19. Nanostructured carbon-crystalline titania composites from microphase separation of poly(ethylene oxide-b-acrylonitrile) and titania sols.

    Science.gov (United States)

    Stefik, Morgan; Lee, Jinwoo; Wiesner, Ulrich

    2009-05-14

    A simple "one-pot" method utilizing a graphitic carbon source containing poly(ethylene oxide-b-acrylonitrile) diblock copolymer as a structure directing agent was used to synthesize carbon-crystalline titania composites as well as crystalline mesoporous titania materials after oxidative carbon removal.

  20. In vivo and in vitro characterization of poly(styrene-b-isobutylene-b-styrene) copolymer stent coatings for biostability, vascular compatibility and mechanical integrity.

    Science.gov (United States)

    Strickler, Fred; Richard, Robert; McFadden, Sharon; Lindquist, Jeff; Schwarz, Marlene C; Faust, Rudolf; Wilson, Gregory J; Boden, Mark

    2010-02-01

    The TAXUS Express 2 Paclitaxel Eluting Coronary Stent System employs a coating consisting of the thermoplastic elastomer, poly(styrene-b-isobutylene-b-styrene; SIBS), selected for its drug-eluting characteristics, vascular compatibility, mechanical properties, and biostability. This study was conducted to evaluate the impact of different SIBS (17-51 mole % styrene) compositions on mechanical properties, chemical stability, and vascular compatibility. Mechanical property (stress-strain measurements) and stability studies were conducted on polymer films with five different styrene contents (17, 24, 32, 39, and 51 mole %). The ultimate tensile strength did not change significantly with composition, but the elongation at break decreased with increased styrene content. A pulsatile fatigue test further confirmed the mechanical stability of SIBS up to 39 mole % styrene. The vascular compatibility of five different SIBS compositions was assessed using SIBS-only coated stents, in the coronary and carotid arteries in a porcine model study. The stability of the vessel wall, rate/degree of endothelialization, inflammation, and thrombus at timepoints from 30 to 180 days were evaluated. The results confirm vascular compatibility over the range of 17-51 mole % styrene.

  1. Absorption cross-sections of the C-h overtone of volatile organic compounds: 2 methyl-1,3-butadiene (isoprene), 1,3-butadiene, and 2,3-dimethyl-1,3-butadiene.

    Science.gov (United States)

    Cias, Pawel; Wang, Chuji; Dibble, Theodore S

    2007-02-01

    Many molecules or transient radicals have well-documented absorption cross-sections in the ultraviolet (UV) region, but their absorption cross-sections in the near-infrared (NIR) region are much less often known and are difficult to measure. We propose a method to determine the unknown NIR absorption cross-sections using the known absorption cross-sections in the UV region, in which single-path UV absorption spectroscopy and NIR continuous wave cavity ringdown spectroscopy (cw-CRDS) are employed in a cross-arm reaction chamber for simultaneous measurements. Without knowing the actual sample partial pressures (or concentrations), the NIR absorption cross-sections can be accurately determined through the two sets of measurements. The method is demonstrated by measuring the NIR absorption cross-section of the first overtone of the asymmetric C-H stretch of 2-methyl-1,3-butadiene (isoprene) (3.24 (+/-0.16) x 10(-22) cm(2) molecule(-1)) at 1651.52 nm using the known value of the absorption cross-section at 220 nm. The diode laser wavelength was calibrated by atmospheric cavity ringdown spectra of CH(4), CO(2), and H(2)O. By comparison with sample pressure measurements, this method can also be used as a pressure calibration means for the reaction chamber, and this has been demonstrated with two additional measurements of the absorption cross-sections of 1,3-butadiene and 2,3-dimethyl-1,3-butadiene (2.50 (+/- 0.08) x 10(-22) and 2.82 (+/-0.16) x 10(-22) cm(2) molecule(-1), respectively) at 1651.52 nm. The applicability of the method to determining absorption cross-sections using the simultaneous measurements of cw-CRDS and single-path absorption spectroscopy is discussed.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2009-10-15

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2013-07-01

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

  4. Synthesis of novel N-, S-substituted-polyhalo-1, 3-butadienes and crystal structure of dibutadienyl homopiperazine

    Indian Academy of Sciences (India)

    Nahide Gulsah Deniz; Cemil Ibis

    2013-07-01

    Polyhalogenated-2-nitro-1, 3-butadienes are important synthetic precursors for a variety of polyfunctionalized bioactive heterocycles. Herein, we report the reactions of 1, 1, 3, 4, 4-pentachloro-2-nitro-1, 3-butadiene 1 and 4-bromo-1, 1, 3, 4-tetrachloro-2-nitro-1, 3-butadiene 2 with amino and thiol containing nucleophiles to obtain highly functionalized (E)-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), mass spectrometry (MS) and Fourier transform infrared spectroscopy (FT-IR) spectroscopic data. Single crystal X-ray structure analysis of compound 8c is reported.

  5. Conversion of ethanol to 1,3-butadiene over Na doped ZnxZryOz mixed metal oxides

    Energy Technology Data Exchange (ETDEWEB)

    Baylon, Rebecca A.; Sun, Junming; Wang, Yong

    2016-01-01

    Despite numerous studies on different oxide catalysts for the ethanol to 1,3-butadiene reaction, few have identified active sites (i.e., type of acidity) correlated to the catalytic performances. In this work, the type of acidity needed for ethanol to 1,3-butadiene conversion has been studied over Zn/Zr mixed oxide catalysts. Specifically, synthesis method, Zn/Zr ratio, and Na doping have been used to control the surface acid-base properties, as confirmed by characterizations such as NH3-TPD and IR-Py techniques. The 2000 ppm Na doped Zn1Zr10Oz-H with balanced base and weak Bronsted acid sites was found to give not only high selectivity to 1,3-butadiene (47%) at near complete ethanol conversion (97%), but also exhibited a much higher 1,3-butadiene productivity than other mixed oxides studied.

  6. PHOTOINDUCED CHARGE TRANSFER POLYMERIZATION OF STYRENE INITIATED BY ELECTRON ACCEPTOR

    Institute of Scientific and Technical Information of China (English)

    CAO Weixiao; ZHANG Peng; FENG Xinde

    1995-01-01

    Photoinduced charge transfer polymerization of styrene(St) with electron acceptor as initiator was investigated. In case of fumaronitrile (FN) or maleic anhydride (MA) as initiator the polymerization takes place regularly, whereas the tetrachloro-1, 4-benzenequinone (TCQ), 2, 3-dichloro-5, 6-dicyano-1, 4-benzenequinone (DDQ) . or tetracyano ethylene (TCNE) as initiator the polymerization proceeds reluctantly only after the photoaddition reaction. A mechanism was proposed that free radicals would be formed following the charge and proton transfer in the exciplex formed between St and electron acceptors.

  7. Poly(styrene-acrylic acid) magnetic polymer microspheres

    Institute of Scientific and Technical Information of China (English)

    Yanling CHENG; Liuqiang MA; Ruohui LI

    2008-01-01

    Magnetic polymer microspheres have been considered as a kind of new biopolymer materials with great advantages in bioseparation engineering and biome-dicine engineering because they have not only polymer functional groups but also magnetic characteristics. Styrene-acrylic acid copolymer (p(S-AA)) magnetic microspheres were synthesized by dispersion polymeriza-tion with Fe3O4 as core and p(S-AA) as shell. The micro-spheres were characterized by SEM, size analysis, molecular weight and solid content measurement. All of them indicate that the microspheres are small in size, nar-row in distribution, stable in chemistry and rich in func-tional groups on their surface.

  8. Copolymerization of Styrene with Dodecyl Methacrylate and Octadecyl Methacrylate

    OpenAIRE

    Vidović, Elvira; SARIĆ, Karla; JANOVIĆ, Zvonimir

    2002-01-01

    Styrene (Sty) was copolymerized with dodecyl methacrylate (DDMA) and with octadecyl methacrylate (ODMA) in toluene solution using 2,2'-azobis(isobutyronitrile) (AIBN) as a free radical initiator over a wide composition and conversion range. The copolymer composi-tion was determined from NMR spectra. The copolymerization reactivity ratios were found to be r1 = 0.52 (Sty) and r2 = 0.42 (DDMA) for the Sty-DDMA system, and r1 = 0.58 (Sty) and r2 = 0.45 (ODMA) for the Sty-ODMA system, showing a te...

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

    Science.gov (United States)

    Ward, C E; Starr, T B

    1993-10-01

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

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

    Science.gov (United States)

    Sakurai, H

    2000-04-01

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

  11. Reversible Addition-Fragmentation Chain Transfer Polymerization of Acrylonitrile under Irradiation of Blue LED Light

    Directory of Open Access Journals (Sweden)

    Zhicheng Huang

    2016-12-01

    Full Text Available Compared to unhealthy UV or γ-ray and high-energy-consumption thermal external stimuli, the promising light emitting diode (LED external stimulus has some outstanding technological merits such as narrow wavelength distribution, low heat generation and energy consumption, and safety for human beings. In this work, a novel reversible addition-fragmentation transfer (RAFT polymerization system for acrylonitrile (AN was developed under the irradiation of blue LED light at room temperature, using 1,2,3,5-tetrakis(carbazol-9-yl-4,6-dicyanobenzene (4CzIPN as a novel radical initiator and 2-cyanoprop-2-yl-1-dithionaphthalate (CPDN as the typical chain transfer agent. Well-defined polyacrylonitrile (PAN with a controlled molecular weight and narrow molecular weight distribution was successfully synthesized. This strategy may provide another effective method for scientific researchers or the industrial community to synthesize a PAN-based precursor of carbon fibers.

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

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

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

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

    Science.gov (United States)

    Page, B D; Charbonneau, C F

    1985-01-01

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

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

    Science.gov (United States)

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

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

  15. Exploiting Framework Flexibility of a Metal-Organic Framework for Selective Adsorption of Styrene over Ethylbenzene

    NARCIS (Netherlands)

    Mukherjee, S.; Joarder, B.; Desai, A.V.; Manna, B.; Krishna, R.; Ghosh, S.K.

    2015-01-01

    The separation of styrene and ethylbenzene mixtures is industrially important and is currently performed in highly energy-intensive vacuum distillation columns. The primary objective of our investigation is to offer an energy-efficient alternative for selective adsorption of styrene by a flexible me

  16. Letter to the Editor: Styrene-producing microbes in food-stuff

    Science.gov (United States)

    An article was published in Journal of Food Science, August 2009 (Vol. 74, Nr 6) entitled “Natural formation of styrene by cinnamon mold flora”. In the article, the authors reported on the production of styrene from several fungi typically found on cinnamon, and used cinnamic acid and similar analog...

  17. EVALUATION OF STYRENE EMISSIONS FROM A SHOWER STALL/BATHTUB MANUFACTURING FACILITY

    Science.gov (United States)

    The report gives results of emissions measurements carried out at a representative facility (Eljer Plumbingware in Wilson, NC) that manufactures polyester-resin-reinforced shower stalls and bathtubs by spraying styrene-based resins onto molds in vented, open, spray booths. Styren...

  18. 21 CFR 173.70 - Chloromethylated aminated styrene-divinylbenzene resin.

    Science.gov (United States)

    2010-04-01

    ... resin. 173.70 Section 173.70 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN... Chloromethylated aminated styrene-divinylbenzene resin. Chloromethylated aminated styrene-divinylbenzene copolymer... resin dispersion. (c) The additive is used as a decolorizing and clarification agent for treatment...

  19. Interaction of styrene with DODAB bilayer vesicles. influence on vesicle morphology and bilayer properties

    NARCIS (Netherlands)

    Jung, M.; Hubert, D.H.W.; Veldhoven, van E.; Frederik, P.M.; Blandamer, M.J.; Briggs, B.; Visser, A.J.W.G.; Herk, van A.M.; German, A.L.

    2000-01-01

    The solubilization of styrene in large unilamellar DODAB vesicles is investigated at a styrene to DODAB molar ratio of 2:1. The combination of various vesicle characterization methods allows a simultaneous look at vesicle morphology (cryo-TEM, DLS) and molecular interactions (micro-DSC, various fluo

  20. Exploiting Framework Flexibility of a Metal-Organic Framework for Selective Adsorption of Styrene over Ethylbenzene

    NARCIS (Netherlands)

    Mukherjee, S.; Joarder, B.; Desai, A.V.; Manna, B.; Krishna, R.; Ghosh, S.K.

    2015-01-01

    The separation of styrene and ethylbenzene mixtures is industrially important and is currently performed in highly energy-intensive vacuum distillation columns. The primary objective of our investigation is to offer an energy-efficient alternative for selective adsorption of styrene by a flexible

  1. Coke formation in the oxidative dehydrogenation of ethylbenzene to styrene by TEOM

    NARCIS (Netherlands)

    Nederlof, C.; Vijfhuizen, P.; Zarubina, V.; Melian-Cabrera, I.; Kapteijn, F.; Makkee, M.

    2014-01-01

    A packed bed microbalance reactor setup (TEOM-GC) is used to investigate the formation of coke as a function of time-on-stream on gamma-Al2O3 and 3P/SiO2 catalyst samples under different conditions for the ODH reaction of ethylbenzene to styrene. All samples show a linear correlation of the styrene

  2. Coke formation in the oxidative dehydrogenation of ethylbenzene to styrene by TEOM

    NARCIS (Netherlands)

    C. Nederlof; P. Vijfhuizen; V. Zarubina; I. Melián-Cabrera; F. Kapteijn; M. Makkee

    2014-01-01

    A packed bed microbalance reactor setup (TEOM-GC) is used to investigate the formation of coke as a function of time-on-stream on γ-Al2O3 and 3P/SiO2 catalyst samples under different conditions for the ODH reaction of ethylbenzene to styrene. All samples show a linear correlation of the styrene sele

  3. EVALUATION OF TRICKLE-BED AIR BIOFILTER PERFORMANCE FOR STYRENE REMOVAL

    Science.gov (United States)

    A pilot-scale trickle-bed air biofilter (TBAB) was evaluated for the removal of styrene from a waste gas stream. Six-millimeter (6 mm) Celite pellets (R-635) were used as the biological attachment medium. The operating parameters considered in the study included the styrene vol...

  4. SYNTHESIS AND CHARACTERIZATION OF COPOLYMER OF 2,5-BIS[(4-METHOXYPHENYL)OXYCARBONYL]STYRENE AND STYRENE WITH HIGH MOLECULAR WEIGHT

    Institute of Scientific and Technical Information of China (English)

    Jiao-li Li; Xing-he Fan; Yong-feng Zhao; Xiao-fang Chen; Qi-feng Zhou

    2004-01-01

    The random copolymers of styrene and 2,5-bis[(4-methoxyphenyloxycarbonyl)styrene] (MPCS) with different copolymerization ratio were synthesized by conventional free radical polymerization. The copolymer having high molecular weight was experimentally elucidated using a combination of proton nuclear magnetic resonance spectroscopy and gel permeation chromatography. The liquid crystalline behavior of the copolymer was studied using differential scanning calorimetry, X-ray diffractometry and polarized optical microscopy. It was found that the liquid crystalline behavior was dependent on the content of styrene. Experimental results show that the copolymer could turn into a liquid crystalline phase at about 180℃ when the content of styrene was less than 20%. The mechanical properties of the copolymer were also studied. Preliminary results indicate that the tensile strength decreases while the tensile modulus increases as the content of MPCS is increased.

  5. The Reproductive Effects Assessment Group's report on the mutagenicity of 1,3-butadiene and its reactive metabolites.

    Science.gov (United States)

    Rosenthal, S L

    1985-01-01

    A major data gap for assessing heritable risk from exposure to 1,3-butadiene is the lack of mammalian mutagenicity data. The data base on the mutagenic potential of 1,3-butadiene is limited to three bacterial studies from the same laboratory. Two of these studies were positive only in the presence of liver S9 mix from chemically pretreated animals. In vitro data suggest that 1,3-butadiene is metabolized to two epoxide intermediates. 3,4-Epoxybutene, one potential reactive metabolite of 1,3-butadiene, is a monofunctional alkylating agent and is a direct-acting mutagen in bacteria. In addition, unpublished data suggest that 3,4-epoxy-butene induces DNA damage and chromosomal aberrations in mice. Another potential reactive metabolite, 1,2:3,4-diepoxybutane, is a bifunctional alkylating agent and is mutagenic in a wide variety of organisms (bacteria, fungi, and the germ cells of Drosophila). This metabolite also induces DNA damage in mice and in cultured hamster cells, is clastogenic in fungi and cultured rat cells, and produces chromosome damage/breakage in Drosophila germ cells. These data, when combined with evidence that 1,3-butadiene is carcinogenic in rodent gonadal tissues and is associated with gonadal atrophy in mice, constitute suggestive evidence that 1,3-butadiene may be a human germ cell mutagen. However, because the mutagenicity of 1,3-butadiene has been studied only in bacteria, studies in mammalian test systems are needed to further characterize the mutagenic potential of 1,3-butadiene.

  6. The Effect of Uncertainty in Exposure Estimation on the Exposure-Response Relation between 1,3-Butadiene and Leukemia

    Directory of Open Access Journals (Sweden)

    George Maldonado

    2009-09-01

    Full Text Available Abstract: In a follow-up study of mortality among North American synthetic rubber industry workers, cumulative exposure to 1,3-butadiene was positively associated with leukemia. Problems with historical exposure estimation, however, may have distorted the association. To evaluate the impact of potential inaccuracies in exposure estimation, we conducted uncertainty analyses of the relation between cumulative exposure to butadiene and leukemia. We created the 1,000 sets of butadiene estimates using job-exposure matrices consisting of exposure values that corresponded to randomly selected percentiles of the approximate probability distribution of plant-, work area/job group-, and year specific butadiene ppm. We then analyzed the relation between cumulative exposure to butadiene and leukemia for each of the 1,000 sets of butadiene estimates. In the uncertainty analysis, the point estimate of the RR for the first non zero exposure category (>0–<37.5 ppm-years was most likely to be about 1.5. The rate ratio for the second exposure category (37.5–<184.7 ppm-years was most likely to range from 1.5 to 1.8. The RR for category 3 of exposure (184.7–<425.0 ppm-years was most likely between 2.1 and 3.0. The RR for the highest exposure category (425.0+ ppm-years was likely to be between 2.9 and 3.7. This range off RR point estimates can best be interpreted as a probability distribution that describes our uncertainty in RR point estimates due to uncertainty in exposure estimation. After considering the complete probability distributions of butadiene exposure estimates, the exposure-response association of butadiene and leukemia was maintained. This exercise was a unique example of how uncertainty analyses can be used to investigate and support an observed measure of effect when occupational exposure estimates are employed in the absence of direct exposure measurements.

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

    Science.gov (United States)

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

    1998-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1997-04-01

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

  9. Synthesis and Characterization of Styrene- Ethylene-Propylene-Styrene (SEPS Grafted with Maleic Anhydride (MAH for Use as Coupling Agent in Wood Polymer Composite

    Directory of Open Access Journals (Sweden)

    M. Acevedo-Morantes

    2015-10-01

    Full Text Available Styrene-Ethylene-Propylene-Styrene (SEPS block copolymer was grafted with maleic anhydride (MAH by reactive extrusion (SEPS-g-MAH using an organic peroxide as initiator in the grafting. SEPS-g-MAH was synthesized for use as coupling agent in wood polymer composite (WPC. Identification of this compatibilizer was made using Fourier transform infrared spectroscopy (FTIR and the grafting degree was determinate with titration. The characteristic peaks in FTIR analysis indicated the presence of MAH in the copolymer.

  10. An integrated approach to biomonitoring exposure to styrene and styrene-(7,8)-oxide using a repeated measurements sampling design.

    Science.gov (United States)

    Fustinoni, S; Campo, L; Manini, P; Buratti, M; Waidyanatha, S; De Palma, G; Mutti, A; Foa, V; Colombi, A; Rappaport, S M

    2008-09-01

    The aim of this work was to investigate urinary analytes and haemoglobin and albumin adducts as biomarkers of exposure to airborne styrene (Sty) and styrene-(7,8)-oxide (StyOX) and to evaluate the influence of smoking habit and genetic polymorphism of metabolic enzymes GSTM1 and GSTT1 on these biomarkers. We obtained three or four air and urine samples from each exposed worker (eight reinforced plastics workers and 13 varnish workers), one air and urine samples from 22 control workers (automobile mechanics) and one blood sample from all subjects. Median levels of exposure to Sty and StyOX, respectively, were 18.2 mg m(-3) and 133 microg m(-3) for reinforced plastics workers, 3.4 mg m(-3) and 12 microg m(-3) for varnish workers, and <0.3 mg m(-3) and <5 microg m(-3) for controls. Urinary levels of styrene, mandelic acid, phenylglyoxylic acid, phenylglycine (PHG), 4-vinylphenol (VP) and mercapturic acids (M1+M2), as well as cysteinyl adducts of serum albumin (but not those of haemoglobin) were significantly associated with exposure status (controls

  11. Influence of the water content and water activity on styrene degeneration by Exophiala jeanselmei in biofilters

    Energy Technology Data Exchange (ETDEWEB)

    Cox, H.H.J. [TNO Inst. of Environmenal Sciences, Energy Research and Process Inovation, Dept. of Environmental Biotechnology, Delf (Netherlands); Magielsen, F.J. [TNO Inst. of Environmenal Sciences, Energy Research and Process Inovation, Dept. of Environmental Biotechnology, Delf (Netherlands); Doddema, H.J. [TNO Inst. of Environmenal Sciences, Energy Research and Process Inovation, Dept. of Environmental Biotechnology, Delf (Netherlands); Harder, W. [TNO Inst. of Environmenal Sciences, Energy Research and Process Inovation, Dept. of Environmental Biotechnology, Delf (Netherlands)

    1996-12-31

    The performance at low water availability of styrene-degrading biofilters with the fungus Exophiala jeanselmei growing on perlite, the inert support, was investigated. E. jeanselmei degrades styrene at a water activity of 0.91-1. In biofilters, the styrene elimination capacity at a water activity of 0.91 is 5% of the maximal elimination capacity of 79 g m{sup -3} h{sup -1} (water activity 1). Application of dry air results in a rapid loss of styrene degradation activity, even at 40%-60% (w/w) water in the filter bed and at a water activity of 1. Humidification of the gas and an additional supply of water to the filter bed are necessary to maintain a high and stable styrene elimination capacity. (orig.)

  12. Organocatalytic chemo- and regioselective oxyarylation of styrenes via a cascade reaction: remote activation of hydroxyl groups.

    Science.gov (United States)

    Zhang, Yu-Chen; Jiang, Fei; Wang, Shu-Liang; Shi, Feng; Tu, Shu-Jiang

    2014-07-01

    The first organocatalytic oxyarylation of styrenes has been established through a cascade of vinylogous Michael addition/alkoxyl transfer reactions of o- or p-hydroxylstyrenes with quinone imine ketals. The process leads to a highly chemo- and regioselective oxyarylation of styrenes and provides access to m-alkylated anilines in generally high yields and excellent diastereoselectivity (up to 99% yield, >95:5 dr). An investigation of the reaction pathway revealed that the existence and position of the hydroxyl group of styrene played crucial roles in the cascade reaction, suggesting that the two reactants were simultaneously activated by binaphthyl-derived phosphoric acid via hydrogen bonding interactions and long-distance conjugative effects. In addition, the activating group of the hydroxyl functionality in the products can be easily removed or transformed, demonstrating the applicability and utility of this strategy in styrene oxyarylation and in the synthesis of styrene-based compounds.

  13. Catalytic and hydrodynamic properties of styrene monooxygenases from Rhocodoccus opacus 1CP are modulated by cofactor binding.

    NARCIS (Netherlands)

    Riedel, A.; Heine, T.; Westphal, A.H.; Conrad, C.; Rathsack, P.; Berkel, van W.J.H.; Tischler, D.

    2015-01-01

    Styrene monooxygenases (SMOs) are flavoenzymes catalyzing the epoxidation of styrene into styrene oxide. SMOs are composed of a monooxygenase (StyA) and a reductase (StyB). The latter delivers reduced FAD to StyA on the expense of NADH. We identified Rhodococcus opacus 1CP as the first microorganism

  14. 40 CFR 721.7020 - Distillates (petroleum), C(3-6), polymers with styrene and mixed terpenes (generic name).

    Science.gov (United States)

    2010-07-01

    ...), polymers with styrene and mixed terpenes (generic name). 721.7020 Section 721.7020 Protection of...), C(3-6), polymers with styrene and mixed terpenes (generic name). (a) Chemical substance and...), polymers with styrene and mixed terpenes (PMN P-89-676) is subject to reporting under this section for...

  15. Genetic and reproductive toxicity of butadiene and isoprene.

    Science.gov (United States)

    Anderson, D

    2001-06-01

    Butadiene (BD) and its 2-methyl analogue, isoprene, have been extensively studied in animals and BD in population studies. Both chemicals are metabolised by liver cytochrome P450 dependent monogenases to monoepoxide and diepoxide intermediates. The diepoxide intermediates of both compounds were mutagenic in Salmonella typhimurium. However, unlike the monoepoxide of BD, the monoepoxides of isoprene were not mutagenic. It appears that they have no alkylating capacity. BD did not induce somatic cell mutation and recombination or sex-linked recessive lethal mutation in Drosophila melanogaster and isoprene produced no increase in chromosomal aberrations in CHO cells in vitro. Comparative concentrations of haemoglobin adducts in the blood of mice and rats after exposure to BD indicated that reaction with blood may decrease the levels of reactive intermediates available to tissues in rats, but not in mice contributing to greater potency of BD in the mouse. For isoprene, the adducts reach approximately the same concentrations in both species. DNA adducts have also been detected in testicular and lung cells of mice after BD exposure. The level of epoxybutene haemoglobin adducts was significantly elevated in BD-exposed workers, but lower than in rats and mice. In conjunction with the toxicology and carcinogenesis studies for BD and isoprene, additional mice were included for the evaluation of cytogenetic effects. Both chemicals produced increases in sister chromatid exchanges in bone marrow cells and in the frequency of micronuclei in normochromatic and polychromatic erythrocytes, but only BD produced an increase in the percent of bone marrow cells with chromosomal aberrations. At similar doses, the effects with BD were 2-3 times larger than with isoprene. There were also increased hprt mutation frequencies in rats and mice after BD exposure. Biomonitoring studies with hprt mutations in lymphocytes showed conflicting results, with both positive and negative findings. BD has

  16. Sulfonated Poly(styrene) Chains Grafted on Magnetic Nanoparticles

    Science.gov (United States)

    Jiao, Yang; Yevelev, Anton; Parra, Javier; Akcora, Pinar; Stevens Institute of Technology Team

    2014-03-01

    Iron oxide nanoparticles functionalized with poly(styrene) (PS) chains at various grafting densities and loadings present stable and ordered nanostructures for tuning the mechanical and conductive properties in polymer composites. Strings, spherical and anisotropic clusters and well-dispersed particles are achieved with PS-grafted Fe3O4 nanoparticles in PS matrices upon varying the system parameters. In this work, we report the effect of sulfonic group locations on the aggregation state of polymer-grafted nanoparticles. Structures formed by the random and diblock copolymers of PS-poly(styrene sulfonate) (PSS) grafted particles will be discussed with small-angle x-ray scattering (SAXS) measurements in solution and melts. The conformational changes in PS-grafted chains and ion-containing grafts will be also presented in small-angle neutron-scattering (SANS) results to understand the role of polymer on the assembly of particles at the low grafting density. We acknowledge support by NSF-CAREER-DMR (#1048865).

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

    Directory of Open Access Journals (Sweden)

    Siti Nurul Ain Md Jamil

    2014-09-01

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

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

    Institute of Scientific and Technical Information of China (English)

    甘永胜; 顾军民; 方永成

    2004-01-01

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

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

    NARCIS (Netherlands)

    Harleman, J.H.; Seinen, W.

    1979-01-01

    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 degene

  20. Palladium-catalyzed 1,4-difunctionalization of butadiene to form skipped polyenes.

    Science.gov (United States)

    McCammant, Matthew S; Liao, Longyan; Sigman, Matthew S

    2013-03-20

    A palladium-catalyzed 1,4-addition across the commodity chemical 1,3-butadiene to afford skipped polyene products is reported. Through a palladium σ → π → σ allyl isomerization, two new carbon-carbon bonds are formed with high regioselectivity and trans stereoselectivity of the newly formed alkene. The utility of this method is highlighted by the successful synthesis of the ripostatin A skipped triene core.

  1. Mechanical Properties of Injection Molded and Compression Molded Samples from Nature-Butadiene Rubber

    OpenAIRE

    Skrobak Adam; Janoštík Václav; Stanek Michal; Manas David; Ovsik Martin; Senkerik Vojtech; Reznicek Martin

    2016-01-01

    The aim of this paper is to show what extent there is an impact on the mechanical properties (tensile strength and tear strength) of a standardized testing sample made of rubber compound based on nature rubber and butadiene rubber produced by injection molding in comparison with a sample produced by classic preparation (cutting out a compression molded plate) according to the standard ISO 23529. For realization of this study it was necessary to design and produce an injection mold for all typ...

  2. Evidence of delayed light emission of TetraPhenyl Butadiene excited by liquid Argon scintillation light

    CERN Document Server

    Segreto, Ettore

    2014-01-01

    TetraPhenyl Butadiene is the wavelength shifter most widely used in combination with liquid Argon. The latter emits scintillation photons with a wavelength of 127 nm that need to be downshifted to be detected by photomultipliers with glass or quartz windows. TetraPhenyl Butadiene has been demonstrated to have an extremely high conversion efficiency, possibly higher than 100% for 127 nm photons, while there is no precise information about the time dependence of its emission. It is usually assumed to be exponentially decaying with a characteristic time of the order of one ns, as an extrapolation from measurements with exciting radiation in the near UV. This work shows that TetraPhenyl Butadiene, when excited by 127 nm photons, reemits photons not only with a very short decay time, but also with slower ones due to triplet states de-excitations. This fact can strongly contribute to clarify the anomalies of liquid Argon scintillation light reported in literature since seventies, namely the inconsistency in the mea...

  3. 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.

  4. 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).

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

    Institute of Scientific and Technical Information of China (English)

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

    2003-01-01

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

  6. In Situ IR Spectroscopic Study on the Hydrogenation of 1,3-Butadiene on Fresh Mo2C/γ-Al2O3 Catalyst

    Institute of Scientific and Technical Information of China (English)

    Zhang Jing; Wu Weicheng; Liu Shiyang

    2014-01-01

    The surface species formed from the adsorption of 1,3-butadiene and 1,3-butadiene hydrogenation over the fresh Mo2C/γ-Al2O3 catalyst was studied by in situ IR spectroscopy. It is found that 1,3-butadiene adsorption on the Mo2C/γ-Al2O3 catalyst mainly formsπ-adsorbed butadiene (πs andπd) andσ-bonded surface species. These species are adsorbed mainly on the surface Moδ+(0<δ<2) sites as evidenced by co-adsorption of 1,3-butadiene and CO on the fresh Mo2C/γ-Al2O3 catalyst. The IR spectrometric analysis show that hydrogenation of 1,3-butadiene over fresh Mo2C/γ-Al2O3 catalyst produces mainly butane coupled with a small portion of butene. The selectivity of butene during the hydrogenation of 1,3-butadiene over fresh Mo2C/γ-Al2O3 catalyst might be explained by the adsorption mode of adsorbed 1,3-butadiene. Additionally, the active sites of the fresh Mo2C/γ-Al2O3 catalyst may be covered by coke during the hydrogenation reaction of 1,3-butadiene. The treatment with hydrogen at 673 K cannot remove the coke deposits from the surface of the Mo2C/γ-Al2O3 catalyst.

  7. Leaching of styrene and other aromatic compounds in drinking water from PS bottles

    Institute of Scientific and Technical Information of China (English)

    Maqbool Ahmad; Ahmad S.Bajahlan

    2007-01-01

    Bottled water may not be safer, or healthier, than tap water. The present studies have proved that styrene and some other aromatic compounds leach continuously from polystyrene (PS) bottles used locally for packaging. Water sapmles in contact with PS were extracted by a preconcentration technique called as "purge and trap" and analysed by gas chromatograph-mass spectrometer (GC/MS). Eleven aromatic compounds were identified in these studies. Maximum concentration of styrene in PS bottles was 29.5 μg/L. Apart from styrene, ethyl benzene, toluene and benzene were also quantified but their concentrations were much less than WHO guide line values. All other compounds were in traces. Quality of plastic and storage time were the major factor in leaching of styrene. Concentration of styrene was increased to 69.53 μg/L after one-year storage time. In Styrofoam and PS cups studies, hot water was found to be contaminated with styrene and other aromatic compounds. It was observed that temperature played a major role in the leaching of styrene monomer from Styrofoam cups. Paper cups were found to be safe for hot drinks.

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

    Directory of Open Access Journals (Sweden)

    Nur Amirah Mohd Zahri

    2015-07-01

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

  9. Cooperativity in CYP2E1 metabolism of acetaminophen and styrene mixtures.

    Science.gov (United States)

    Hartman, Jessica H; Letzig, Lynda G; Roberts, Dean W; James, Laura P; Fifer, E Kim; Miller, Grover P

    2015-10-01

    Risk assessment for exposure to mixtures of drugs and pollutants relies heavily on in vitro characterization of their bioactivation and/or metabolism individually and extrapolation to mixtures assuming no interaction. Herein, we demonstrated that in vitro CYP2E1 metabolic activation of acetaminophen and styrene mixtures could not be explained through the Michaelis-Menten mechanism or any models relying on that premise. As a baseline for mixture studies with styrene, steady-state analysis of acetaminophen oxidation revealed a biphasic kinetic profile that was best described by negative cooperativity (Hill coefficient=0.72). The best-fit mechanism for this relationship involved two binding sites with differing affinities (Ks=830μM and Kss=32mM). Introduction of styrene inhibited that reaction less than predicted by simple competition and thus provided evidence for a cooperative mechanism within the mixture. Likewise, acetaminophen acted through a mixed-type inhibition mechanism to impact styrene epoxidation. In this case, acetaminophen competed with styrene for CYP2E1 (Ki=830μM and Ksi=180μM for catalytic and effector sites, respectively) and resulted in cooperative impacts on binding and catalysis. Based on modeling of in vivo clearance, cooperative interactions between acetaminophen and styrene resulted in profoundly increased styrene activation at low styrene exposure levels and therapeutic acetaminophen levels. Current Michaelis-Menten based toxicological models for mixtures such as styrene and acetaminophen would fail to detect this concentration-dependent relationship. Hence, future studies must assess the role of alternate CYP2E1 mechanisms in bioactivation of compounds to improve the accuracy of interpretations and predictions of toxicity.

  10. Organolanthanide Compounds Containing Methanesulfonate and Pyrazinamide Ligand in Styrene Polymerization

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The synthesis of organolanthanide compounds identified as LnCp*(MS)2PzA, Ln=Sm, Tb, Yb (MS=methanesulfonate, Cp*=pentamethylcyclopentadienyl, and PzA=pyrazinamide), by the reaction of coordination compounds Ln(MS)3(PzA)4 with NaCp in THF was reported. The complexes were formulated according to elemental analyses, complexometric titration with EDTA (%Ln), and 1H NMR. IR spectroscopy revealed that PzA coordinates with lanthanide(Ⅲ) ions and methanesulfonate coordinates via oxygen atoms in a non-equivalent manner. In preliminary catalytic studies, these compounds were active in styrene polymerization that used MAO as a cocatalyst with an activity of 12.3 kg PS mol Sm-1h-1. Differential scanning calorimetry (DSC) of polystyrene showed that the polymer was mainly atactic.

  11. Interacting Blends of Novel Unsaturated Polyester Amide Resin with Styrene

    Directory of Open Access Journals (Sweden)

    Hasmukh S. Patel

    2004-01-01

    Full Text Available Novel unsaturated poly (ester-amide resins (UPEAs were prepared by the reaction between an epoxy resin, namely diglycidyl ether of bisphenol–A (DGEBA and unsaturated aliphatic bisamic acids using a base catalyst. These UPEAs were then blended with a vinyl monomer namely, Styrene (STY. to produce a homogeneous resin syrup. The curing of these UPEAs-STY. resin blends was carried out by using benzoyl peroxide (BPO as a catalyst and was monitored by using a differential scanning calorimeter (DSC. The glass fibre reinforced composites (i.e. laminates of these UPEA-STY. resin blends were fabricated using the DSC data. The chemical, mechanical and electrical properties of the glass fibre composites have also been evaluated. The unreinforced cured samples of the UPEA-STY. resin blends were also analyzed by thermogravimetry (TGA.

  12. Simulation of styrene polymerization reactors: kinetic and thermodynamic modeling

    Directory of Open Access Journals (Sweden)

    A. S. Almeida

    2008-06-01

    Full Text Available A mathematical model for the free radical polymerization of styrene is developed to predict the steady-state and dynamic behavior of a continuous process. Special emphasis is given for the kinetic and thermodynamic models, where the most sensitive parameters were estimated using data from an industrial plant. The thermodynamic model is based on a cubic equation of state and a mixing rule applied to the low-pressure vapor-liquid equilibrium of polymeric solutions, suitable for modeling the auto-refrigerated polymerization reactors, which use the vaporization rate to remove the reaction heat from the exothermic reactions. The simulation results show the high predictive capability of the proposed model when compared with plant data for conversion, average molecular weights, polydispersity, melt flow index, and thermal properties for different polymer grades.

  13. 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.

  14. 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.

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

    Institute of Scientific and Technical Information of China (English)

    戴洪雁; 陈福林; 岑兰; 周彦豪

    2010-01-01

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

  16. 2-Cyanoethylmercapturic acid (CEMA) in the urine as a possible indicator of exposure to acrylonitrile.

    Science.gov (United States)

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

    1987-12-01

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

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

    Science.gov (United States)

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

    2014-09-26

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

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

    Science.gov (United States)

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

    1999-08-01

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

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

    Science.gov (United States)

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

    2009-01-01

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

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

    Directory of Open Access Journals (Sweden)

    2007-01-01

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

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

    Science.gov (United States)

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

    2016-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

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

    2005-01-01

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

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

    Science.gov (United States)

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

    2016-03-01

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

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

    Directory of Open Access Journals (Sweden)

    Danish J Malik

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

  5. Reaction of pyrocatechol and resorcinol with styrene in the presence of aluminum phenolate

    Energy Technology Data Exchange (ETDEWEB)

    Kozlikovskii, Y.B.; Butov, S.A.; Koshchii, V.A.

    1986-08-01

    The alkylation of pyrocatechol and resorcinol with styrene in the presence of aluminum phenolate leads to a mixture of isomeric (..cap alpha..-methylbenzyl)dihydroxybenzenes, in which the ortho-alkylation products as a rule predominate.

  6. EPR investigation on radiation-induced graft copolymerization of styrene onto polyethylene: Energy transfer effects

    Science.gov (United States)

    Salih, M. A.; Buttafava, A.; Ravasio, U.; Mariani, M.; Faucitano, A.

    2007-08-01

    In this paper, energy transfer phenomena concerning the in-source graft copolymerization of styrene onto LDPE were investigated through the EPR analysis of the radical intermediates. The model solution experiments have shown a substantial deviation of the experimental G (radicals) values with respect to the additivity law, which reflect the negative effect of the styrene monomer concentration on the initiation rate of the graft copolymerization. The EPR measurements performed on polyethylene- co-styrene graft copolymers of various composition following low-temperature vacuum gamma irradiation have confirmed the decrease of the total radical yields with increasing the styrene concentration. The effect was partly attributed to the heterogeneity of the graft copolymer matrix and to the lack of molecular mobility in the solid state at low temperature, which prevents the attainment of the favourable geometrical configurations in intermolecular energy and charge transfer events.

  7. 21 CFR 573.870 - Poly(2-vinylpyridine-co-styrene).

    Science.gov (United States)

    2010-04-01

    ...-vinylpyridine-co-styrene) may be safely used as nutrient protectant in feed for beef cattle and dairy cattle and... rumen-stable, abomasum-dispersible nutrient(s) for beef cattle and dairy cattle and replacement dairy...

  8. PALLADIUM-CATALYZED OXIDATION OF STYRENE AND ALKENES IN PRESENCE OF IONIC LIQUIDS (WACKER REACTION)

    Science.gov (United States)

    The use of ionic liquids in various synthetic transformations is gaining significance due to the enhanced reaction rates, potential for recycling and compatibility with various organic compounds and organometallic catalysts. Palladium-catalyzed oxidation of styrene and other alk...

  9. Prediction of Phase Behavior for Styrene/CO2/Polystyrene Mixtures

    Institute of Scientific and Technical Information of China (English)

    吴家龙; 潘勤敏; 等

    2002-01-01

    A lattice fluid model,Sanchez-Lacombe equation,is used to predict the phase behavior for a styrene/CO2/polystyrene ternary system.The binary parameters involved in the equation were optimized using experimental data.Phase diagrams and the distribution coefficients of styrene between polymer phase and fluid phase are obtained over a wide rang of pressure,temperature and composition.The analysis of ternary phase diagrams indicates that this system at relatively high pressure or low temperature may display two-phase equilibrium,and at low pressures or high temperatures three-phase equilibrium may appear.The distribution coefficients of styrene between the fluid phase and the polymer phase increase asymptotically to unity when the concentration of styrene increases.The results provide thermodynamic knowledge for further exploitation of supercritical carbon dioxide assisted devolatilization and impregnation.

  10. Combustion products of 1,3-butadiene inhibit catalase activity and induce expression of oxidative DNA damage repair enzymes in human bronchial epithelial cells

    OpenAIRE

    2008-01-01

    1,3-Butadiene, an important petrochemical, is commonly burned off when excess amounts need to be destroyed. This combustion process produces butadiene soot (BDS), which is composed of a complex mixture of polyaromatic hydrocarbons in particulates ranging in size from

  11. Updated evaluation of the migration of styrene monomer and oligomers from polystyrene food contact materials to foods and food simulants.

    Science.gov (United States)

    Genualdi, Susan; Nyman, Patricia; Begley, Timothy

    2014-04-01

    Due to the 2011 labelling of styrene monomer as "reasonably anticipated to be a human carcinogen" by the National Institutes of Health's National Toxicology Program (NTP) and the controversy over whether styrene oligomers mimic the physiological effects of estrogen, an updated review of styrene monomer and oligomers in food and food contact materials (FCMs) was performed. The concentrations of styrene monomer and oligomers were determined in 24 polystyrene (PS) products and ranged from 9.3 to 3100 mg kg(-1) for the styrene monomer, 130-2900 mg kg(-1) for the sum of three styrene dimers, and 220-16,000 mg kg(-1) for the sum of six styrene trimers. Foods in contact with PS packaging had styrene monomer concentrations ranging from 2.6 to 163 ng g(-1); dimer concentrations from the limit of quantitation (LOQ) to 4.8 ng g(-1) and trimer concentrations were all below the LOQ (2 ng g(-1)). Diffusion coefficients (Dp) and partition coefficients (K) were also calculated for styrene dimers and trimers. The results presented here indicate that styrene monomer concentrations in foods have not significantly changed since the 1980s and monomer concentrations in food packaging quantified in this study were all below USFDA limits. Although styrene dimers and trimers are present in higher concentrations in PS FCMs than the monomer, their migration to food is limited because of their high K values (4 × 10(2) to 2 × 10(6)) and their low diffusion coefficients in PS products. Additionally, diffusion coefficients calculated using USFDA-recommended food simulants and Arrhenius plots describing the temperature dependence of styrene dimers and trimers can be used in future calculations of dietary intake of the styrene oligomers.

  12. THE EFFECT OF POLAR ADDITIVES ON THE γ RADIATION INDUCED POLYMERIZATION OF STYRENE

    Institute of Scientific and Technical Information of China (English)

    ZHANG Xujia; HA Hongfei; WU Jilan; WEI Genshuan

    1994-01-01

    The γ induced polymerization of styrene in the presence of polar additives such as tributyl phosphate, triethyl amine and ethanol was studied at dose rate of 5.0 × 1017 eV/ml. min. The result shows that radiation induced polymerization of styrene was sensitized by the three kinds of additives at the approximate same rate and the experimental results were in agreement with the theoretical calculation of WAS equation. The cause of sensitization is due to the proton transfer.

  13. Mechanical and molecular studies of biocomposites filled with oil palm empty fruit bunches microfibers

    Science.gov (United States)

    Nikmatin, S.; Saepulloh, D. R.; Irmansyah; Syafiuddin, A.

    2017-05-01

    The present work aims to investigate mechanical and molecular characteristics of acrylonitrile butadiene styrene (ABS) composites filled with oil palm empty fruit bunches (OPEFB) microfibers. OPEFB microfibers were produced using mechanical milling. Composite granules were fabricated using single screw extruder. These composites were then used for fabricating helmet according to the Indonesian National Standard (SNI). Mechanical testing confirms that the helmet produced using this biocomposites are suitable to the SNI. Molecular interaction between matrix with OPEFB can be described using orbital hybridization theory. In general, this study has successfully investigated mechanical and molecular properties of the biocomposites.

  14. Development of recycled plastic composites for structural applications from CEA plastics

    Science.gov (United States)

    Bhalla, Agrim

    Plastic waste from consumer electronic appliances (CEAs) such as computer and printer parts including Polystyrene (PS), Acrylonitrile Butadiene Styrene (ABS), Polystyrene (PS) and PC/ABS were collected using handheld FTIR Spectrophotometer. The blends of these plastics with High Density Polyethylene (HDPE) are manufactured under special processing conditions in a single screw compounding injection molding machine. The blends are thermoplastics have high stiffness and strength, which may enhance the mechanical properties of HDPE like tensile modulus, ultimate tensile strength, tensile break and tensile yield. These composites have a potential to be used for the future application of recycled plastic lumber, thus replacing the traditional wood lumber.

  15. Rapid prototyping of polymeric microstructures with a UV laser

    DEFF Research Database (Denmark)

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

    2003-01-01

    By laser ablation of Poly-Ether-Ether-Ketone (PEEK), a negative master of the microsystem was produced. This master is then used for hot embossing of a number of polystyrene (PS) parts. A few hundred replications can be made without warping and alteration of the dimensions. The possibility of using...... 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...

  16. Analysis of Strength on Thick Plate Part using Genetic Algorithm Optimisation Method

    Directory of Open Access Journals (Sweden)

    Azlan S.M.

    2016-01-01

    Full Text Available This study focuses on the optimisation of the injection moulding parameters to maximise the strength ofmoulded parts using a simulation software. The moulded parts were injected with Acrylonitrile- Butadiene-Styrene (ABS whereas mould temperature, melt temperature, packing pressure and packing time were selected as variable process parameters. The polynomial model obtained using Design of Experiment (DOE was integrated with the Response Surface Methodology (RSM and Centre Composite Design (CCD. The RSM was supported with Genetic Algorithm (GA to anticipate the optimum value of processing parameters with the highest strength. It was found that strength of the parts can be improved 2.2% using the methodology reported herein.

  17. Production of super-smooth articles

    Energy Technology Data Exchange (ETDEWEB)

    Duchane, D.V.

    1981-05-29

    Super-smooth rounded or formed articles made of thermoplastic materials including various poly(methyl methacrylate) or acrylonitrile-butadiene-styrene copolymers are produced by immersing the articles into a bath, the composition of which is slowly changed with time. The starting composition of the bath is made up of at least one solvent for the polymer and a diluent made up of at least one nonsolvent for the polymer and optional materials which are soluble in the bath. The resulting extremely smooth articles are useful as mandrels for laser fusion and should be useful for a wide variety of other purposes, for example lenses.

  18. Cooling simulation of plastic injection molding

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Analyses the cooling of mold and plastic part during injectionmolding and the continued cooling of plastic part after being ejected from mold using the heat transfer theory and Boundary Element Method (BEM) to predict the temperature distribution in both mold and plastic part,and presents the experiments carried out with plates of ABS (Acrylonitrile-Butadiene-Styrene) to verify the validity of the cooling analysis software used to simulate the temperature distribution in ABS plate parts, and concludes that the analysis software agree qualitatively well with actual experimental findings.

  19. A low-cost lead-acid battery with high specific-energy

    Indian Academy of Sciences (India)

    S K Martha; B Hariprakash; S A Gaffoor; D C Trivedi; A K Shukla

    2006-01-01

    Lightweight grids for lead-acid battery grids have been prepared from acrylonitrile butadiene styrene (ABS) copolymer followed by coating with lead. Subsequently, the grids have been electrochemically coated with a conductive and corrosion-resistant layer of polyaniline. These grids are about 75% lighter than those employed in conventional lead-acid batteries. Commercial-grade 6V/3.5Ah (C20-rate) lead-acid batteries have been assembled and characterized employing positive and negative plates constituting these grids. The specific energy of such a lead-acid battery is about 50 Wh/kg. The batteries can withstand fast charge-discharge duty cycles.

  20. Mechanical Spectroscopy of Nanostructured Composite Materials

    Energy Technology Data Exchange (ETDEWEB)

    Mari, Daniele; Schaller, Robert; Mazaheri, Mehdi, E-mail: daniele.mari@epfl.ch [Ecole Polytechnique Federale de Lausanne, Laboratoire de Physique de la Matiere Complexe, Groupe de Spectroscopie Mecanique, CH-1015 Lausanne (Switzerland)

    2011-07-06

    The thermo-mechanical behavior of different nano-structured composite materials, which were processed within the SAPHIR European Integrated Project, has been characterized by mechanical spectroscopy. The obtained results show clearly that creep resistance of fine grain ceramics such as zirconia can be improved by carbon nano-tube (CNT) reinforcements. On the other hand the elastic modulus and the damping capacity of aluminum matrix composites were increased by SiC nano-particle additions. It has also been observed that CNT additions are responsible for a better thermal stability of polymer such as ABS (Acrylonitrile-Butadiene-Styrene) used in automotive industry.