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81.
High temperature, high pressure e.s.r. measurements of the hydrogenation reaction of Taiheiyo coal in the presence of catalysts were carried out to understand the stabilization of thermally and/or catalytically induced free radicals. A decrease in free radical concentration with increasing temperature was observed for ZnCl2 and SnCl2 · 2H2O catalysts at 10MPa under hydrogen gas. High pressure modified single-cell d.t.a. and p.d.a. equipment augmented the uniquely designed high temperature, high pressure e.s.r. cell. The hydrogenation reaction was monitored under the same experimental conditions as for e.s.r. From the results of the combination of high temperature, high pressure e.s.r. with high pressure d.t.a. and p.d.a., it was established that H2 molecules can react efficiently with free radicals from coal molecules created by the presence of ZnCl2 and SnCl2 · 2H2O catalysts.  相似文献   
82.
Four cocatalysts, referred to as ethylaluminoxanes, were synthesized by the reaction between triethylaluminium (AIEt3) and water under various molar ratios of H2O/Al at ?78°C. Aluminoxanes were used as cocatalysts for a MgCl2‐supported Ziegler–Natta catalyst for propylene polymerization at temperatures ranging from 70 to 100°C. When the polymerization was activated by AlEt3, the activity as well as the molecular weight and isotacticity of the resulting polymer gradually dropped as the temperature varied from 70 to 100°C. When ethylaluminoxane was employed as the cocatalyst, good activity and high molecular weight and isotacticity were obtained at 100°C. Furthermore, when the cocatalyst varied from AlEt3 to ethylaluminoxane, the atactic fraction and polymer fraction with moderate isotacticity decreased and the high isotactic fraction slightly increased, which indicated that the variation of the cocatalyst significantly affects the isospecificity of active sites. It was suggested that the reactivity of the Al‐Et group and the size of the cocatalyst were correlated to the performance of the Ziegler–Natta catalyst at different temperatures. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1978–1982, 2006  相似文献   
83.
Taisuke Ito 《Polymer》1982,23(10):1412-1434
Results for the compressibilities of a wide range of polymer crystals along the fibre- and the transverse crystal axes are presented. Good agreement is found between the theoretical and the experimental results of different authors.  相似文献   
84.
M.K.V. Chan  J.G. Williams 《Polymer》1983,24(2):234-244
The phenomenon of slow stable crack growth in polyethylene is investigated using notched specimens subject to constant load and the concepts of fracture mechanics. The effect of specimen geometry and dimension, the loading and the mode of loading on the applied stress intensity factor versus crack speed (Kc-a?) curves has been studied to demonstrate that Kc is the controlling stress parameter for crack growth under suitable conditions. Kc-a? curves are obtained for a high density polyethylene homopolymer in distilled water and in a diluted detergent solution at four different temperatures. Results are also obtained for a much tougher medium density polyethylene copolymer whenever possible. Several mechanisms can be identified from the form of the Kc-a? curves. Two, in particular, have been observed but not explained before: (i) crack growth with a time dependence of 0.25, and (ii) the high Kc-a? slopes for crack growth in a tough copolymer. With the help of scanning electron microscopic studies of the fracture surfaces, (i) is postulated to be due to diffusion controlled void growth process and (ii) is considered to be the result of crack tip blunting effects. From the temperature dependence of crack growth, the activation energy of the diffusion controlled crack growth process is found to coincide with that of the x-relaxation process in polyethylene implying that diffusion controlled crack growth may be related to the motion of main chains in the polymer.  相似文献   
85.
徐德锋 《云南化工》1997,(1):48-49,5
采用Nova-Pak C18不锈钢色谱柱进行反相液相色谱分析,以甲醇:水=65:35(V/V)为注动相,以邻苯二甲醇二乙酯为内标物,用内标法测定田草灵除草剂中苄嘧黄隆和异丙甲草胺的含量,结果表明,各有效成分与内标物色谱峰分离完全,杂质无干扰,测定结果,苄嘧黄隆和异丙甲草胺的变异系数分别为0.74%和1.07%,回收率分别为99.4% ̄100.8%和99.1% ̄101.3%。  相似文献   
86.
The creep and creep fracture behavior of two hot-pressed aluminas are presented, for both flexural and tensile testing. Steady-state power-law creep is observed with a stress exponent of about 2 for each material. Three distinct fracture regimes are found. At high stress in flexure, fracture occurs by slow crack growth with a high stress dependence of the failure time. At intermediate stresses, in both flexure and tension, creep fracture occurs by multiple microcracking after modest strains. Failure times exhibit a modest stress dependence (stress exponent of 2.5 in tension and 3 in flexure), with a constant failure strain equal to 0.09. The failure times are considerably longer in flexure than in tension, because of the constraint imposed on crack growth by the bending geometry. We conclude that flexure cannot be used for creep lifetime assessment, even in simple, single-phase materials such as Al2O3. At low stresses, in tension, failure also exhibits a modest stress dependence but with a much higher failure strain. The material shows the onset of super-plastic behavior.  相似文献   
87.
通过对高抗冲聚苯乙烯树脂出现产品落锤指标偏低问题的分析,从橡胶配量及其粒径大小上进行了改进,同时改进了工艺操作,采取了提高反应釜搅拌速度、降低乙苯浓度等措施。结果产品合格率达到99%以上,优级品率达到98%以上。  相似文献   
88.
原位聚合制备尼龙6/纳米SiO2复合材料研究   总被引:10,自引:0,他引:10  
对原位聚合制备尼龙6/纳米SiO2进行研究。结果表明,无论是否对纳米SiO2复合材料进行偶联化处理,其表面均将在原位聚合过程中与尼龙6产生接枝;SiO2表面接枝物的生成,可在某种程度上造成体系结晶程度的降低,但复合体系的力学性能主要由SiO2粒子的分散程度、粒子和其体之间的相界面性质等因素决定;采用经偶联剂处理并具有较小粒径和较大比表面积的SiO2对尼龙6进行复合,可使复合体系的力学性能指标达到较高的水平,且硅烷偶联剂的最佳用是为SiO2的3%左右。  相似文献   
89.
在使用无底柱分段崩落法的矿山,大都存在着地压现象。其主要表现是采矿进路和联络道的变形破坏。对采矿进路在开挖和回采过程中各阶段受力情况的分析表明,进路的变形、破坏主要是受到岩体初始静应力、爆破动应力和矿柱支撑应力的综合作用的结果。  相似文献   
90.
I. Narisawa  T. Murayama  H. Ogawa 《Polymer》1982,23(2):291-294
The brittle fracture of round-notched epoxy resin bars subjected to plane strain bending has been studied at varying strain rates. Observations of fracture processes and surface morphologies revealed that the internal crack was nucleated at the plastic-elastic boundary when the plastic deformation zone at the notch root reached a certain size. A slip-line field theory allows calculation of the stress components at the plastic-elastic boundary from a knowledge of the location of the internal crack. An analysis of the data concluded that the triaxial stress level ahead of the plastic zone was raised by plastic constraints to an ideal fracture stress which is considerably larger than that of glassy thermoplastics.  相似文献   
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