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reaction formation相关的网络例句

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

Transmission Electron Microscope and other properties testing results show that the complex emulsifier system is the crucial influence factor of the polymerization process and the properties of products. It may influence the coagulum content and reaction rate of the polymerization process, the performance, particle diameter,viscosity, electrolyte stability and storage stability of the emulsion products and the contact angle of the film.The initiator mainly influences the coagulum content and reaction rate.The acrylic monomers mainly influence the solid content, Minimum Film Formation Temperature of the emulsion and the Glass Transition Temperature of the film.The organic silicone monomer mainly influences the water absorption of the film.The reaction temperature mainly influences the reaction rate and conversion.The stirring intensity mainly influences the coagulum content of the polymerization process.

透射电镜等性能测试结果显示:复合乳化剂体系是硅丙共聚乳液的聚合过程及产品性能的主要影响因素,它可以对聚合过程的凝胶率、反应速率以及乳液的外观、粒径、粘度、耐电解质稳定性及贮存稳定性,还有乳液涂膜的接触角等造成不同程度的影响;引发剂主要影响反应速率和凝胶率;丙烯酸酯单体主要影响到乳液的固含量、最低成膜温度以及涂膜的玻璃化转变温度,有机硅单体主要影响涂膜的吸水率等;聚合反应温度主要影响乳液的反应速率和转化率等;搅拌强度主要是影响到聚合过程的凝胶率。

The first ethynyl group is reacted with the first reactive group in a first carbon-carbon bond formation reaction and the second ethynyl group is reacted with the second reactive group in a second carbon-carbon bond formation reaction to crosslink the first backbone with the second backbone, thereby forming the packaging substrate.

在第一个碳-碳键生成反应中,使第一个乙炔基与第一个反应性基反应,在第二个碳-碳键生成反应中,使第二个乙炔基与第二个反应性基反应,将第一种主链与第二种主链交联,从而制成组装基片。

The whole sintering process of SHS converter fettling materials can be divided into three steps. The first step is the decomposition reaction of carbonates and sodium nitrate, which is an endothermic reaction. The second step is the SHS reaction, i. e. thermite reaction, the metal of Al reacts with CO〓, O〓, NO〓, Fe〓O〓 to form Al〓O〓. The speed of thermite reaction is very quick, and accompanied with large amount of heat emission and temperature rise. The third step is the reaction of spinels formation. The Al〓O〓 produced by SHS reacts with MgO to form spinels.

整个SHS补炉料的烧结过程分三步进行:第一步为碳酸盐、硝酸钠的分解反应,属于吸热反应;第二步为SHS反应即铝热反应,金属铝粉与CO〓、O〓、NO〓、Fe〓O〓等反应生成Al〓O〓,反应速度很快,并伴随有巨大的放热和温度升高;第三步为合成尖晶石的反应,SHS反应产物Al〓O〓与MgO反应生成尖晶石。

At present,the rate laws and reaction mechanisms of pyrite oxidation,pyrite and chalcopyrite formation,uraninite and magnetite dissolution in aqueous solutions are mainly studied,and it is discovered that (1)oxidation rate of pyrite controlled by surface reaction assume fractional dependence on Fe3+ and O2 molalities in acid solutions;(2)Pyrite cannot nucleate directly from solutions below 300 ℃,it can only form initially through sulfidation of a FeS precursor. The rate equation of reaction between FeS and H2S to form pyrite is of the second order;(3)Chalcopyrite is formed by reactions of pyrrhotite or pyrite with Cu2+,the former proceeds via a series of mediate metastable phases of Cu-Fe sulfide,whereas the rate equation of the latter is apparently of the first order which is controlled by surface reaction;(4)The nonlinear behavior of magnetite dissolution at acid pH can be represented by a shrinking core model coupling with surface reaction and diffusion transport.

目前主要研究了水溶液中黄铁矿氧化、黄铁矿和黄铜矿形成、晶质铀矿和磁铁矿溶解的速率定律和反应机理,发现:(1)酸性溶液中黄铁矿的氧化速率对Fe3+和O2浓度呈分数依赖并受表面反应的控制;(2)低于300 ℃时黄铁矿不能从溶液中直接成核,而需初始地通过FeS先驱物的硫化生成,FeS与H2S反应形成黄铁矿的速率方程为二级;(3)磁黄铁矿或黄铁矿与Cu2+反应均可形成黄铜矿,前者经历了一系列准稳的Cu-Fe硫化物的中间物,后者的速率方程为表观一级并受表面反应的控制;(4)酸性pH时磁铁矿的非线性溶解行为可采用表面反应扩散输运耦合的收缩核模型来描述。

Prolonging nitration time and increasing reaction temperature would promote the formation of dinitro products while shortening the nitration time and decreasing reaction temperature would promote the formation of mono-nitro products.

延长反应时间和提高反应温度有利于二硝化产物的形成,缩短反应时间和降低反应温度有利于单硝化产物的形成。

Four phenylalanine derivatives were synthesized with this approach. The condition of the condensation reaction was optimized. The side reaction of the Curtius reaction was studied and a urine by-product was isolated and characterized.b. Through the detailed study of the behavior of various N-acetyl phenylalanine methyl esters under the condition of the Bischler-Napieralski reaction, it was found for the first time that the formation of benzyl oxazole derivatives was a competitive approach with the normal B-N reaction.

一、基于Bischler-Napieralski反应设计了以苯丙氨酸衍生物为原料的路线,在这条路线的研究中,主要取得了以下结果:、建立了一条以芳香醛和丙二酸单甲酯为原料,通过缩合、氢化、Curtius等反应制备苯丙氨酸甲酯的通用合成路线,对其中的缩合反应条件及Curtius反应中的副反应进行了深入的研究,利用这条路线合成了四个芳环取代的苯丙氨酸单甲酯衍生物。

The side reaction of the Curtius reaction was studied and a urine by-product was isolated and characterized.b. Through the detailed study of the behavior of various N-acetyl phenylalanine methyl esters under the condition of the Bischler-Napieralski reaction, it was found for the first time that the formation of benzyl oxazole derivatives was a competitive approach with the normal B-N reaction. A convincing mechanism was suggested and a rule governing the reaction was summarized.c.

一、基于Bischler-Napieralski反应设计了以苯丙氨酸衍生物为原料的路线,在这条路线的研究中,主要取得了以下结果:、建立了一条以芳香醛和丙二酸单甲酯为原料,通过缩合、氢化、Curtius等反应制备苯丙氨酸甲酯的通用合成路线,对其中的缩合反应条件及Curtius反应中的副反应进行了深入的研究,利用这条路线合成了四个芳环取代的苯丙氨酸单甲酯衍生物。

The first step in the degradation is most probably the classical ester scission reaction to give a carboxylic acid and olefinic end groups. Further ester scission on the adjacent ester groups of carboxylic acid and olefinic molecular chains can then lead to the formation of lower weight pyrolytic products, such as: CH〓=CHOCOPhCOOCH=CH〓、CH〓=CHOCOPhCOOH and HOOCPhCOOH, and they can pyrolyze continually to produce substrate pyrolytic compounds, such as: HOOCPhCOCH〓、PhCOOH、PhH、PhCOCH〓 and CO、CO〓. At the same time, a corsslinking cyclization reaction occurred of the formation of the gas products during the degradation of PET.

断裂大分子链端邻近羰基和乙烯基的酯键持续断裂,不断地形成小分子裂解产物,如:CH〓=CHOCOPhCOOCH=CH〓、CH〓=CHOCOPhCOOH以及HOOCPhCOOH,这些产物还会进一步裂解成分子量更低的小分子裂解产物,如:HOOCPhCOCH〓、PhCOOH、PhH、PhCOCH〓以及CO、CO〓等,与此同时,一部分乙烯基酯端基的大分子链碎片会发生支化而相互连接,再经&链脱离&和环化反应形成难燃的交联产物。

The effect of single factor indicated that lower concentration of tea polyphenols and oxidant, temperature, ester proportion and pH value, shorter reaction time were favorable to the formation and accumulation of TFs, higher concentration of tea polyphenols, temperature, ester proportion and pH value, longer reaction time were favorable to the formation and accumulation of TRs.

借助参数模型研究各参数因子对TFs和TRs形成的影响,结果表明:茶多酚浓度、温度、酯比例及pH值对TFs和TRs形成与积累均有显著影响,反应时间对TFs影响显著,氧化剂对TRs影响显著;单因素效应显示:较低的茶多酚和氧化剂浓度、适当的低温和较短的时间、低的酯比例和pH较有利于TFs形成与积累,而有利于TRs形成与积累的参数则相反。

The interfacial chemistry, synergistic effects and interfacial kinetics of thesynergistic extraction system D_2EHPA-MPA-Fe~(3+) have been studied, where MPA is amono-alkyl phosphate extraction with long carbon chain. D_2EHPA in the mixed extractionsystem strongly exhibits the effect on the thermodynamics of micella formation and interfaceproperties of MPA. Some thermodynamic parameters of micella formation were obtained.The interfacial adsorption behaviour of D_2EHPA is opposite to that of MPA. Theemulsification for single MPA and the mixed system was discussed. The synergistic effectswere found in this mixed extraction system. It is proved that the process of Fe~(3+) extractionfor non-mixed extraction system is controlled by chemical reaction, the controlling reactionoccurs at the interface, and the reaction rate equation is obtained.

本文研究了协同萃取体系D_2EHPA—MPA—Fe~(3+的胶团形成热力学、界面特性、协萃效应和界面动力学(动力学控制机制和反应速率方程)研究发现,混合萃取体系中的D_2EHPA强烈地影响MPA的胶团形成热力学和界面吸附行为,得到了胶团生成常数、胶团形成自由能和临界胶团浓度的热力学参数D_2EHPA和MPA具有相反的界面吸附行为研究发现D_2EHPA—MPA混合萃取剂体系对Fe~(3+)产生了协萃效应动力学和界面化学的研究结果还证实了非胶束混合萃取体系的Fe~(3+)的萃取过程是受化学反应控制的,控制反应发生在界面上

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