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reaction rate相关的网络例句

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与 reaction rate 相关的网络例句 [注:此内容来源于网络,仅供参考]

The non-isothermal decomposition kinetics of nylon 1010 and nylon 1010/POSS composites in nitrogen were investigated. POSS significantly increased the activation energy but had little effect on the reaction order.(5) Exploring research was carried out on the reaction between EVM and nylon 1010. The reaction between EVM and TsOH during melt mixing was also invesigated, and related reaction mechanisms were studied in terms of NMR, TGA-FTIR and etc.

五初步研究了乙烯-醋酸乙烯酯橡胶和尼龙1010在高温下的反应性,报道了EVM和TsOH在高温条件下的反应性,通过核磁共振、热重-红外联用等分析表征方法探索了相关的反应机理,EVM和TsOH反应后,EVM的耐溶剂性、玻璃化转变温度和力学性能均有所提高,而体积电阻率则显著下降。

The results show that the reactive characters of macro-kinetics are different from that of intrinsic kinetics under the same experimental conditions. The isobutene dimeric reaction follows 1.5 order reaction because of the effect of inner diffusion, and isooctane dimeric reaction follows zero order reaction.

结果表明,在相同的实验条件下,反应的宏观动力学行为与本征动力学行为有较大的不同,异丁烯的反应级数受内扩散影响由2级变为1.5级,异辛烯的反应级数则为0级。

The reaction kinetics was studied by selecting control-step method as well as modified Debye-Hückel activity coefficient model and Bromley osmotic coefficient model. The results show that the reaction order is 2 and apparent reaction activation energy 85.8 kJ/mol, and the reaction is mainly controlled by precipitation of KB5O8?4H2O.

采用选取控制步骤法并引入修正的Debye-Hückel活度系数模型和Bromley渗透系数模型研究了该反应的动力学的影响规律,得出反应级数为2,表观反应活化能为85.8 kJ/mol,反应主要受四水五硼酸钾晶体析出的控制。

The controlling factor of the polymerization rate is varied from the diffusion rate of monomers to the addition rate. In this case, the variation of polymerization rate is very small, and is close to first-order reaction.

控制聚合速率的主要因素则从单体的扩散速率过渡到单体的滴加速率,而聚合速率几乎不随时间变化、接近一级状态。

The results show that the initial phase is non-homogeneous reaction,solid-liquid mass transfer coefficient is the main factor on the reaction rate,N-methyl-2-pyrrolidone can accelerate the dissolution of polyester film and prompte the alcoholysis reaction into homogeneous process.

结果表明,反应初始阶段为非均相阶段,固-液间传质系数是影响反应速率的主要因素,加入NMP可以加速PET的溶解,促使醇解反应快速进入均相阶段。

The effect to rate of production of the reaction active of different alkaline earth, the reaction efficiency of different low-carbon alcohols and reaction time were investigated.

考察了不同碱土金属、不同低碳醇及反应时间对醇盐产率的影响。

The results indicate that the optimized sulfonylation reaction time is 4 h, the materiel rate of chlorosulfonic acid and 2-chloroimidazo[1,2-α]pyridine is 1.2 : 1, with ethylamine the yield increasing from 15.4% to above 70%; the optimized ammonolysis reaction time is 3 h and the reaction temperature is 27℃, with the acetonitrile yield increasing from 60.1% to above 79.6%.

实验结果表明,磺酰化反应的最佳反应时间为4 h,氯磺酸与2-氯咪唑并[1,-α]吡啶的用量比为1.2:1,加入三乙胺可将收率由15.4%提高到70%以上;氨解反应的最佳反应时间为3 h,反应温度为27 ℃,加入乙腈可将收率由60.1%提高到79.6%;方案经改进后,总反应时间缩短3 h,收率提高了5.5%。

The results show that the oxidation process of arsenopyrite is speeded up with increasing concentration of FeCl3solution and rising temperature of reaction within the temperature range of 15~35℃, whereas the reaction rate of arsenopyrite is reduced at 45℃, and that the arsenic released from the reaction of arsenopyrite with FeCl3acidic solutions whose concentration is lower than 1×10-4mol·kg-1is in the form of As, which is likely to be soon oxidized into As in the FeCl3acidic solution.

结果显示:在温度为 15~35℃内,毒砂的氧化随FeCl3溶液浓度增加和反应温度升高而加速,而45℃时毒砂的反应速率反而降低;毒砂在与氧化剂FeCl3酸性溶液(浓度小于1×10-4mol·kg-1)反应时释放到溶液中的砷为As,As在FeCl3酸性溶液中很快被氧化成As。

The comparison of hydrolysis-polycondensation reaction and microstructure of ORMOSILs derived by TEOS, MTES, VTES, ETES confirms that the influence of organic group such as methyl, vinyl, ethyl and ethoxyl on the hydrolysis and polycondensation reaction rate depends on several factors including electron-donating capability, size and number of ethoxyl group which can participates polycondensation reaction.

确认甲基、乙烯基和乙基和乙氧基等改性基团对硅醇盐水解-缩聚反应速度的影响是取决于有机改性基团的电负性、尺寸和可水解的-OR基团数目等因素综合作用的结果,其水解速度依MTES>TEOS>VTES>ETES的顺序递减。由于Si原子上可聚合的基团数目减少,导致MTES、VTES和ETES的聚合反应速度降低,而与水解速率失配。

The gas-solid reaction mechanism was studied in the tank reactor. It was found that the reaction rate was controlled by the interdiffusion and intrinsic chemical reaction.

在釜式反应器内研究了氯磺化反应的气固相反应机理,发现气体的内扩散和本征化学反应是氯磺化反应的控制步骤。

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