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环氧化天然橡胶的研究与应用 总被引:5,自引:0,他引:5
环氧化天然橡胶(ENR)是由NR化学改性而成,笔者阐述了环氧化天然橡胶制备原理和方法、环氧化天然橡胶性能及应用研究、环氧化天然橡胶共混改性研究,其中包括ENR与PVC共混体系的研究、ENR其它共混体系的研究和ENR改性的研究. 相似文献
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研究环氧化天然橡胶(ENR)和偶联剂Si69对芳纶帘线与天然橡胶(NR)粘合性能的影响。结果表明:随着ENR用量的增大,NR胶料的门尼焦烧时间缩短,硫化胶的硬度、拉断伸长率和撕裂强度增大,100%定伸应力和H抽出力先增大后减小,当ENR用量为10份时,NR胶料的综合性能最佳;在间-甲-白粘合体系中,加入偶联剂Si69的NR胶料门尼粘度减小,门尼焦烧时间延长,硫化胶的硬度和定伸应力增大,H抽出力减小,而加入ENR的NR胶料门尼粘度增大,门尼焦烧时间缩短,硫化胶的300%定伸应力减小,H抽出力增大。 相似文献
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就环氧化天然橡胶(ENR)和乙烯丙烯酸酯橡胶(EAA)两组分增容剂对白炭黑填充天然橡胶(NR)/再生胶粉(RRP)并用胶的硫化特性、机械性能、溶胀性和形态进行了研究。结果表明,对于白炭黑填充NR/RRP并用胶,加入ENR/EAA可缩短硫化时间t90,改善加工性能和提高交联密度,还可提高诸如拉伸强度、定伸应力和硬度等机械性能。机械性能的改善是由于加入ENR/EAA两组分增容剂使白炭黑与NR/RRP并用胶之间的交联密度得到提高和相互作用有所改善的缘故。 相似文献
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研究环氧化天然橡胶(ENR)在全钢载重子午线轮胎胎面胶中的应用。结果表明:用ENR部分取代天然橡胶(NR),胶料的门尼粘度增大,焦烧时间延长,强伸性能略有下降,抗湿滑性能显著改善,耐磨陛能提高,压缩生热略有升高。 相似文献
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通过偶联剂KH550改性白炭黑与助分散剂TA修饰石墨烯发生迈克尔加成反应形成强杂化键得到白炭黑/石墨烯杂化填料,研究胶料配方中不同偶联剂KH550用量改性的白炭黑/石墨烯杂化填料在天然橡胶(NR)胶料中的分散性和对NR胶料性能的影响。结果表明,与未使用偶联剂KH550的NR硫化胶相比,用量为2份的偶联剂KH550改性的白炭黑/助分散剂TA修饰的石墨烯杂化填料的NR硫化胶的拉伸强度最大(27.8 MPa)、压缩生热最低、玻璃化温度最低(-37.06 ℃)、热导率最大(在30和150 ℃下的热导率分别为0.168和0.184 W·m-1·K-1),硫化胶中白炭黑的聚集明显减弱,硫化胶的综合性能最佳。 相似文献
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Natural rubber (NR), epoxidized natural rubber (ENR), and chlorosulfonated polyethylene (CSM) composites filled with conductive carbon black and aluminum powder have been prepared by using a two‐roll mill. An electromagnetic interference shielding effectiveness of those rubber composites was carried out in the frequency range of 8–12GHz (X‐band microwave). The increase of filler loading enhanced shielding effectiveness of the rubber composites. Conductive carbon black was more effective in shielding than aluminum powder. Binary filler‐filled rubber composites showed higher shielding effectiveness than that of single filler‐filled rubber composites. It has been observed that the shielding effectiveness of these rubber composites could be ranked in the following order: ENR ≥ CSM > NR, whereas the mechanical properties of the rubber composites were in the order of CSM > ENR > NR. The correlation between shielding effectiveness and electrical conductivity as well as mechanical properties of the rubber composites are also discussed. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 相似文献
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Effect of surface modification of silicon carbide nanoparticles on the properties of nanocomposites based on epoxidized natural rubber/natural rubber blends 下载免费PDF全文
Improvement of the properties of rubber nanocomposites is a challenge for the rubber industry because of the need for higher performance materials. Addition of a nanometer‐sized filler such as silicon carbide (SiC) to enhance the mechanical properties of rubber nanocomposites has rarely been attempted. The main problem associated with using SiC nanoparticles as a reinforcing natural rubber (NR) filler compound is poor dispersion of SiC in the NR matrix because of their incompatibility. To solve this problem, rubber nanocomposites were prepared with SiC that had undergone surface modification with azobisisobutyronitrile (AIBN) and used as a filler in blends of epoxidized natural rubber (ENR) and natural rubber. The effect of surface modification and ENR content on the curing characteristics, dynamic mechanical properties, morphology and heat buildup of the blends were investigated. The results showed that modification of SiC with AIBN resulted in successful bonding to the surface of SiC. It was found that modified SiC nanoparticles were well dispersed in the ENR/NR matrix, leading to good filler‐rubber interaction and improved compatibility between the rubber and filler in comparison with unmodified SiC. The mechanical properties and heat buildup when modified SiC was used as filled in ENR/NR blends were improved. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45289. 相似文献
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Thermoplastic natural rubber based on polyamide‐12 (PA‐12) blend was prepared by melt blending technique. Influence of blending techniques (i.e., simple blend and dynamic vulcanization) and types of natural rubber (i.e., unmodified natural rubber (NR) and epoxidized natural rubber (ENR)) on properties of the blends were investigated. It was found that the simple blends with the proportion of rubber ~ 60 wt % exhibited cocontinuous phase structure while the dynamically cured blends showed dispersed morphology. Furthermore, the blend of ENR exhibited superior mechanical properties, stress relaxation behavior, and fine grain morphology than those of the blend of the unmodified NR. This is attributed to chemical interaction between oxirane groups in ENR molecules and polar functional groups in PA‐12 molecules which caused higher interfacial adhesion. It was also found that the dynamic vulcanization caused enhancement of strength and hardness properties. Temperature scanning stress relaxation measurement revealed improvement of stress relaxation properties and thermal resistance of the dynamically cured ENR/PA‐12 blend. This is attributed to synergistic effects of dynamic vulcanization of ENR and chemical reaction of the ENR and PA‐12 molecules. Furthermore, the dynamically cured ENR/PA‐12 blend exhibited smaller rubber particles dispersed in the PA‐12 matrix. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011 相似文献
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P. L. Teh Z. A. Mohd Ishak A. S. Hashim J. Karger‐Kocsis U. S. Ishiaku 《应用聚合物科学杂志》2004,94(6):2438-2445
Onium modified montmorillonite (organoclay) was compounded with natural rubber (NR) in an internal mixer and cured by using a conventional sulfuric system. Epoxidized natural rubber with 50 mol % epoxidation (ENR 50) in 10 parts per hundred rubber (phr) was used as a compatibilizer in this study. For comparison purposes, two commercial fillers: carbon black (grade N330) and silica (grade vulcasil‐S) were used. Cure characteristics were carried out on a Monsanto MDR2000 Rheometer. Organoclay filled vulcanizate showed the lowest values of torque maximum, torque minimum, scorch, and cure times. The kinetics of cure reaction showed organoclay could behave as a cocuring agent. The mechanical testing of the vulcanizates involved the determination of tensile and tear properties. The improvement of tensile strength, elongation at break, and tear properties in organoclay filled vulcanizate were significantly higher compared to silica and carbon black filled vulcanizates. In terms of reinforcing efficiency (RE), organoclay exhibited the highest stiffness followed by silica and carbon black filled vulcanizates. Scanning electron microscopy revealed that incorporation of various types of fillers has transformed the failure mechanism of the resulting NR vulcanizates compared to the gum vulcanizates. Dynamic mechanical thermal analysis (DMTA) revealed that the stiffness and molecular relaxation of NR vulcanizates are strongly affected by the filler–rubber interactions. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 2438–2445, 2004 相似文献
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Rubber toughened poly(lactic acid) (PLA) was prepared by blending with natural rubber (NR)‐based polymers. The blends contained 10 wt % of rubber and melt blended with a twin screw extruder. Enhancement of impact strength of PLA was primarily concernced. This study was focused on the effect of rubber polarity, rubber viscosity and molecular weight on mechanical properties of the blends. Three types of rubbers were used: NR, epoxidized natural rubber (ENR25 and ENR50), and natural rubber grafted with poly(methyl methacrylate) (NR‐g‐PMMA). Effect of viscosity and molecular weight of NR, rubber mastication with a two‐roll mill was investigated. It was found that all blends showed higher impact strength than PLA and NR became the best toughening agent. Viscosity and molecular weight of NR decreased with increasing number of mastication. Impact strength of PLA/NR blends increased after applying NR mastication due to appropriate particle size. DMTA and DSC characterization were determined as well. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011 相似文献
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