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研究钕系顺丁橡胶(Nd BR)在全钢载重子午线轮胎胎面胶[天然橡胶(NR)/顺丁橡胶(BR)并用胶]中的应用。结果表明:在全钢载重子午线轮胎胎面胶中采用Nd BR(BR CB22和BR CB24)等量替代镍系顺丁橡胶(Ni BR)(BR9000),胶料的F_(max)较大,t_(90)和t_(100)延长,抗硫化返原性能改善,拉伸性能、抗撕裂性能、耐磨性能、耐老化性能和耐疲劳性能提高,动态生热和压缩疲劳生热降低;与采用BR CB24的胎面胶相比,采用BR CB22的胎面胶的动态生热和压缩疲劳生热更低,综合性能更好;采用BR CB22的胎面胶的成品轮胎滚动阻力降低。 相似文献
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研究两种国产稀土顺丁橡胶(Nd BR)Nd-40和Nd-60分别在全天候轮胎和冬季轮胎胎面胶中的应用性能,并与传统镍系顺丁橡胶(BR9000)进行对比。结果表明:与BR9000相比,两种Nd BR与填料的结合能力较好,加工工艺性能可满足现场生产要求;两种Nd BR硫化胶的综合物理性能和耐热老化性能较优,抗湿滑性能相近,滞后损失小,生热低,成品轮胎的高速和耐久性能均符合产品设计要求;在全天候轮胎胎面胶中加入Nd-40,硫化胶的耐磨性能提高,成品轮胎的滚动阻力降低。 相似文献
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《轮胎工业》2018,(8)
研究高乙烯基聚丁二烯橡胶(HVBR)等量部分替代溶聚丁苯橡胶(SSBR)或天然橡胶(NR)在高性能半钢子午线轮胎胎面胶中的应用。结果表明:HVBR等量部分替代NR用于轮胎胎面胶,其拉伸强度、撕裂强度、拉断伸长率、弹性和耐压缩疲劳性能均得以改善,但其耐磨性能、动态生热性能及滚动阻力性能均变差;HVBR等量部分替代SSBR用于轮胎胎面胶,可在保证高抗湿滑性能的同时,提高胶料的力学强度、硬度、耐压缩疲劳性能和耐磨性能,并降低动态生热、滚动阻力和密度,满足"绿色轮胎"的节能和高性能轮胎的性能要求。成品轮胎测试结果表明,相比于生产配方轮胎,采用HVBR等量部分替代SSBR胎面胶的轮胎耐磨性能略好,动力性能较好,滚动阻力、高速和耐久性能、干地操控性能和经济性相当。 相似文献
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对载重斜交轮胎胎面胶配方进行改进。通过减小NR用量,增大BR9000用量,以白炭黑部分替代炭黑,可改善炭黑的分散性,提高胶料的耐压缩疲劳性能和耐磨性能,有利于消除胎面胶在实际使用中出现的崩花、掉块现象,降低滚动阻力和生热,提高成品轮胎的速度性能和耐久性。 相似文献
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研究超细全硫化粉末丁苯橡胶(UFPSBR)对天然橡胶(NR)/丁苯橡胶/顺丁橡胶(BR)胎面胶性能的影响。结果表明:与未加UFPSBR的胎面胶相比,加入2~3份UFPSBR的NR/溶聚丁苯橡胶/BR胎面胶拉伸强度略有减小,耐磨性能和抗湿滑性能提高,生热降低;加入1~2份UFPSBR的NR/乳聚丁苯橡胶/BR胎面胶拉伸强度增大,抗湿滑性能略有提高,滚动阻力变化不大,耐磨性能下降。 相似文献
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我厂3号回转窑(Φ4m×60m)生产线在1996年年底由SP窑(产量912t/d)改为NSP窑(产量1320t/d),预分解系统为四级旋风预热器带离线式分解炉 相似文献
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乙烯酮(双乙烯酮)是十分重要的化工中间体,其下游产品较多。江苏某化工厂开发生产乙烯酮(双乙烯酮)下游产品三十多个,年生产规模三万多吨,是国内以乙烯酮(双乙烯酮)为中间体生产精细化学品的综合骨干企业。针对乙烯酮(双乙烯酮)下游产品废水特点,该厂结合企业实际,开展了产品优化,结构调整,清洁生产,资源循环利用,节水降耗等工作,从源头削减了污染物的生产。同时投资二千多万元新建预处理装置三套,6000m3/d废水生化处理装置一套,使全厂乙烯酮(双乙烯酮)下游产品的废水得到了有效的治理。 相似文献
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The miscibility of various amorphous polybutadienes with mixed microstructures of 1,4 addition units (cis, 1,4 and trans 1,4) and 1,2 addition units have been investigated. The studies here involved optical transparency, differential scanning calorimetry, and small angle light scattering. It was found that a 90 percent (cis) 1, 4 addition polybutadiene was immiscible with high (91 percent) 1,2 addition polybutadiene. Reduction of the 1,2 content to 71 percent induced an upper critical solution temperature (UCST) with the cis 1,4 polymer. Polybutadienes with 50 percent and 10 percent 1,2 contents were miscible above the crystalline melting temperature of the cis 1,4 polybutadiene. Immiscibility of the 91 percent 1,2 addition polymer was also found with a 10 percent 1,2 polybutadiene. The latter polymer also exhibits an UCST with the 71 percent 1,2 polymer. The results are used to interpret the characteristics of blends of polybutadienes of varying microstructure. 相似文献
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以F类粉煤灰为例,详细介绍了测定粉煤灰中烧失量的步骤、计算数学模型、影响测量不确定度的因素以及各项测量不确定度分量评定,人员、设备、材料、方法、环境都是影响测量不确定的因素。 相似文献
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The objective of the study was to explore the effect of the degree of deacetylation (DD) of the chitosan used on the degradation rate and rate constant during ultrasonic degradation. Chitin was extracted from red shrimp process waste. Four different DD chitosans were prepared from chitin by alkali deacetylation. Those chitosans were degraded by ultrasonic radiation to different molecular weights. Changes of the molecular weight were determined by light scattering, and data of molecular weight changes were used to calculate the degradation rate and rate constant. The results were as follows: The molecular weight of chitosans decreased with an increasing ultrasonication time. The curves of the molecular weight versus the ultrasonication time were broken at 1‐h treatment. The degradation rate and rate constant of sonolysis decreased with an increasing ultrasonication time. This may be because the chances of being attacked by the cavitation energy increased with an increasing molecular weight species and may be because smaller molecular weight species have shorter relaxation times and, thus, can alleviate the sonication stress easier. However, the degradation rate and rate constant of sonolysis increased with an increasing DD of the chitosan used. This may be because the flexibilitier molecules of higher DD chitosans are more susceptible to the shear force of elongation flow generated by the cavitation field or due to the bond energy difference of acetamido and β‐1,4‐glucoside linkage or hydrogen bonds. Breakage of the β‐1,4‐glucoside linkage will result in lower molecular weight and an increasing reaction rate and rate constant. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 3526–3531, 2003 相似文献