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研究天然橡胶(NR)的相对分子质量对全钢载重子午线轮胎胎体胶性能的影响,并使用不同方法对NR的相对分子质量进行表征。结果表明:NR的相对分子质量与胶料的门尼粘度呈正相关性,与胶料的门尼焦烧时间和自粘性呈负相关性;RSS3硫化胶的综合物理性能最优,10#标准胶硫化胶的综合物理性能最差;在一定区间内的NR相对分子质量与硫化胶的H抽出力呈强相关性;NR的塑性初值和门尼粘度只能粗略地表征NR的相对分子质量,复数粘度可以有效地表征NR的相对分子质量。 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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研究相对分子质量(门尼粘度)及其分布对反式1,4-丁二烯-异戊二烯共聚橡胶(TBIR)性能的影响。结果表明,TBIR的塑炼、混炼性能随着门尼粘度的减小逐渐改善,门尼粘度大于60的TBIR混炼难度增大、加工性能变差;TBIR的综合物理性能随着门尼粘度的增大而提高,但当门尼粘度大于55之后胶料物理性能和动态性能改善效果不显著,TBIR胶料综合性能在门尼粘度为50~60时达到最佳。相对分子质量分布呈双峰的TBIR生胶和硫化胶的强伸性能、磨耗性能和生热性能较优;相对分子质量分布呈单峰的TBIR硫化胶耐屈挠性能得到很大提高。 相似文献
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研究反式异戊橡胶(TPI)的门尼粘度对天然橡胶(NR)/TPI减震性能的影响。结果表明:与NR硫化胶相比,NR/TPI硫化胶的硬度增大,拉伸性能和抗撕裂性能降低,压缩永久变形减小,在-30,23和70 ℃下的耐屈挠龟裂性能提高,但在100 ℃×48 h热老化后23 ℃下的耐屈挠龟裂性能降低;随着TPI门尼粘度的提高,NR/TPI硫化胶的拉伸性能、撕裂强度和回弹值提高,静态压缩永久变形、动静刚度比和损耗因子减小,耐压缩疲劳性能以及在-30,23和70 ℃下的耐屈挠龟裂性能提高;高门尼粘度TPI在橡胶减震制品中的应用性能更优异。 相似文献
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将纳米微珠二氧化硅添加至空气弹簧用天然橡胶(NR)胶料中,研究纳米二氧化硅用量对NR胶料的加工性能和物理性能以及空气弹簧耐疲劳性能的影响。结果表明:随着纳米微珠二氧化硅用量的增大,NR胶料的硫化特性和门尼粘度未发生明显变化,NR硫化胶的邵尔A型硬度先减小后增大,300%定伸应力无明显变化,拉伸强度和拉断伸长率呈减小趋势;当纳米微珠二氧化硅用量为10~15份时,NR硫化胶的耐屈挠性能较佳;在空气弹簧用NR胶料中加入10份纳米微珠二氧化硅能够有效地提高空气弹簧的耐常温疲劳性能和耐高温疲劳性能。 相似文献
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研究有机硅乳液用量对天然橡胶(NR)/丁苯橡胶(SBR)并用胶性能的影响。结果表明:随着有机硅乳液用量的增大,NR/SBR并用胶的门尼粘度和FL减小,表明有机硅乳液可改善并用胶的加工性能;NR/SBR并用胶的t10和t90缩短,表明有机硅乳液会降低并用胶的加工安全性,但可提高并用胶的硫化速率;NR/SBR并用胶的拉伸强度、拉断伸长率和撕裂强度和DIN磨耗量先增大后减小,Payne效应先增强后减弱。当有机硅乳液用量为6.8份时,NR/SBR并用胶的物理性能、耐磨性能和炭黑分散性最好。 相似文献
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研究了ZnO、硬脂酸(SA)对天然橡胶(NR)开炼机塑炼特性的影响。结果表明,开炼机薄通法塑炼NR时,长分子链率先断裂,导致相对分子质量分布变窄,中等相对分子质量级分数量增多,小分子级分变化不大;ZnO和SA均能加快NR长分子链的断裂,门尼粘度下降更快,SA对NR有化学塑解剂的作用,塑炼胶中中等相对分子质量和低相对分子质量级分增多,可以减少薄通次数3~5次;ZnO和SA同时加入NR中塑炼时,塑炼胶的门尼粘度下降很快,塑炼胶中中等相对分子质量和低相对分子质量级分明显增多,较纯NR塑炼可以减少薄通次数8~10次,大大提高了开炼机薄通法塑炼效率。 相似文献
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苯乙烯是重要的石油化工原料。本文介绍了国内外苯乙烯生产的发展概况,合成乙苯,苯乙烯所用的催化剂种类,并就苯乙烯生产及催化剂的发展趋势提出了自己的观点。 相似文献
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Synthesis and characterization of homopolymers and copolymers of various acrylates and acrylonitrile
Various homopolymers and copolymers of methyl acrylate, ethyl acrylate, butyl acrylate, and acrylonitrile in different feed ratios were synthesized. These were characterized by IR, 13C-NMR, DSC, DTA, and TGA. Spectroscopic characterization helped in differentiating copolymers of different mol ratios. Thermal analysis revealed different degradation patterns for homopolymers and copolymers. The temperature and energy changes associated with various phase transitions were dependent on the chemical composition of homo- and copolymers, as expected. © 1993 John Wiley & Sons, Inc. 相似文献
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The variation of the Au 4f binding energy of Au clusters with the cluster size has been established by measuring the binding energies of clusters whose size distributions were independently determined by HREM and STM. The binding energy increases significantly when the cluster size is less than 2 nm. Au-Cu bimetallic clusters of the composition Cu3Au have been deposited for the first time on carbon substrates. The shifts in the core level binding energies of the bimetallic clusters show the effect of alloying in the case of large clusters, but show effects of both alloying and cluster size in the case of the small clusters. The interaction of CO with Cu3Au clusters is stronger than with a bulk Cu metal. The interaction of CO with small Cu clusters also seems to be stronger than with bulk Cu or with large Cu clusters. 相似文献
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《国际聚合物材料杂志》2012,61(1-4):113-122
Abstract Kinetics and mechanisms of oxidation of 6 acetals by molecular oxygen and ozone in liquid phase have been studied. Reaction with molecular oxygen (70°C, 15–16 hr) leads to the formation monoethers of the corresponding glycols with 68–90% selectivity. Salts of metals and complexes with crown-ethers have increased the reaction rate significally. Ozone have reacted with acetals with formation similar products. The mechanisms of intermediate stages have been proposed. 相似文献
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G. R. Hamed 《The Journal of Adhesion》1983,16(1):31-39
A substantially greater detachment energy is required to strip a polyethylene tereph-thalate (Mylar) film from a styrene-butadiene-styrene (SBS) triblock copolymer compared to that for peeling from a random styrene-butadiene (SBR) copolymer. This is true even though the intrinsic interaction between the Mylar and each elastomer is expected to be similar because of their virtually identical chemical composition. It is proposed that this difference in peel strength (between the SBS and SBR) is a consequence of the much higher dissipative capacity of the former elastomer. Another manifestation of this is the higher cohesive tear strength of the SBS compared to the SBR. Extents of energy dissipation within each elastomer during detachment of the Mylar adherend are consistent with the hypothesis that the average maximum stress experience before detachment is some similar fraction of each elastomer's tensile strength. 相似文献
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Polypentafluorostyrene (PPFS), polymethylacrylate (PMA), and poly(pentafluorostyrene-co-methylacrylate), poly(PFS-co-MA) were prepared and the wetting characteristics of polymer blends of PPFS and PMA were compared with that of poly(PFS-co-MA) via contact angle measurements. The critical surface tension of polypentafluorostyrene was found to be 22.6 dyne/cm, which is comparable to the value reported for polytrifluoroethylene (22 dyne/cm). The critical surface tension of poly(PFS-co-MA) is not linearly related to its composition. The polymer blends of PPFS and PMA exhibit significant surface enrichment of the fluoropolymer. The harmonic-mean method1 was employed to determine surface tensions of these polymers and many known polymers. It is found that the method produces useful surface tension data provided the contact angle values are derived from testing liquids of dissimilar polarity. 相似文献
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