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Kinetics analysis showed that the photochemical reaction kinetics of 4,4'-DI3B was pseudo-first order reaction in n-hexane solution, and the reaction was a process of debromination step by step.

动力学分析表明,4,4'-DBB在正己烷中的光化学反应为准一级反应,是一个逐步脱溴的反应过程。

The analysis of thermal behavior and chemical structure show that the three main reactions do not initiate simultaneously. Dehydrogenization and cyclization reactions begin at the initial stage of stabilization, while oxidation reaction takes place on the precondition of cyclization reaction. Cyclization reaction has induction period that is influenced by temperature and heating rate.

热分析和化学结构分析的结果表明,预氧化过程中的三大主要反应并非同时进行,脱氢反应和环化反应从预氧化初期开始,而氧化反应需要以环化反应为前提条件,随后进行;环化反应具有一定的诱导期;在氧化性气氛中,首先发生脱氢反应,氧对环化反应起到了阻碍作用,使整个过程顺利可控。

Two estolide are that the ester melts an agent take amylum as raw material , with smooth butylene , the ester carrying out the solid room's spends reaction under the situation of there being no menstruum,ester composing smooth amylum butylene diacid Shan, and by having optimized reaction condition , having improved reaction efficiency.

以淀粉为原料,以顺丁烯二酸酐为酯化剂,在无溶剂的情况下,进行固体间的酯化反应,合成淀粉顺丁烯二酸单酯,并通过优化反应条件,提高了反应效率。

The synthetic process of dialkyl phosphate by reaction of long -chain alcohol with phosphorus oxychloride was studied. The influence of molar ratio of reactants, reaction temperature, reaction time on process of esterification and hydrolysis was investigated too.

研究了以三氯氧磷与正构偶数高碳醇为原料合成磷酸二长直链烷基酯(C10~16-DAP)的工艺条件,考察了物料配比、反应温度和反应时间等因素对酯化反应与水解反应进程的影响,通过正交实验方法,确定了优化的合成工艺条件。

The third part of this thesis is reactive simulating calculation In this section, some well-known auxiliaries are selected to compute in density functional theory B3LYP on Gaussian 03, from which the relationship between reaction active energies of transition states and enantiomeric excess of chiral products homoallylic alcohols isobtained based on relative reactive ratio theory. Using this relationship, calculations on the reaction of more than eight auxiliaries with four other aldehydes are carried out in AMI and MNDO, proving that N,N\'-dibenzyl tartamide has higher enantioselectivity than others in this reaction.

第三部分为计算化学部分,运用密度泛函理论B3LYP方法在Gaussian03软件上对已经报道的几种手性配体参与的醛不对称烯丙基化反应过程进行模拟计算,基于相对反应速率理论找出两种构型过渡态间活化能的差异与产物光学收率之间的关系;并以此为基础,用AM1和MNDO方法对上述合成的几种配体控制的反应过程进行量化计算,从而在理论上证实了N-苄基酒石酸二酰胺配体在醛的不对称烯丙基化反应中具有较高的立体选择性。

Utilizing 6 and several kinds of diazides prepared in our lab, polys containing 1,2,3-triazolyl and perfluorocyclobutane units were synthesized by "Click chemistry". Utilizing the polycondensation reaction between 6 and several commercially available aromatic diphenol or copolymerization reaction after adding another active aromatic dichloride, fluorinated polys containing phenylphosphine oxide units were synthesized. Utilizing the polycondensation reaction between 6 and several commercially available aromatic dianhydride, fluorinated polys containing PPO units were synthesized.Secondly, structure characterization of fluorinated polys.

利用化合物6同各种自制的二叠氮化合物,通过&Click chemistry&,合成了具有1,2,3-三唑环结构单元的全氟环丁基类聚芳醚;利用化合物22同各种商业化的芳香二元酚类化合物进行缩聚反应或者再加入另外一种活性芳香二氯代物进行三元共聚反应,制备了具有苯基氧膦结构单元的含氟聚芳醚;通过化合物25同各种商业化的芳香二元酸酐类化合物进行缩聚反应,得到了具有PPO结构单元的含氟聚醚酰亚胺。

The reaction performance of Pt-Sn-Li/Al_2O3/FeCrAl catalyst was measured,and the properties of the catalyst were characterized.It was found that reaction temperature,LHSV and the molar ratio of hydrogen to alkane have greatly affected on the catalytic performance of the Pt-Sn-Li/Al_2O_3/FeCrAl catalyst.Under a set of optimal reaction conditions,at 0.1 MPa,470℃,the molar ratio of hydrogen to alkane of 4 and LHSV of 0.14 mL·m~(-2)·h~(-1),the dodecane conversion is 6%,and the dodecene selectivity is about 72%.

结果表明:工业催化剂的催化性能比至今实验室制备的γ-Al_2O_3和SBA-15颗粒负载型颗粒状催化剂的性能好;反应温度、液时空速和氢烃摩尔比对Pt-Sn-Li/Al_2O_3/FeCrAl金属基整体式催化剂脱氢性能都有重要影响,最适宜的反应条件是压力为0.1 MPa,反应温度为470℃,进料氢烃摩尔比为4和LHSV为0.14 mL·m~(-2)·h~(-1),此时十二烷的转化率约为6%,十二烯的选择性约为72%;活性组分涂层与金属基体结合良好。

In this paper, synthetic process of PTT and cationic dyeable PTT was studied, including molar ratio, catalyst concentration, reaction time and temperature, types of antioxidants in the esterification reaction and the condensation reaction.

研究了聚对苯二甲酸丙二醇酯、阳离子染料可染PTT的合成工艺条件中各因素对酯化及缩聚反应的影响,包括单体物质的量比、催化剂浓度、反应时间和温度、抗氧剂种类等。

He best reaction conditions of TMAA were as follows: p-benzenediol as the polymerization inhibitor and the amount 1% of acrylic acid, reaction temperature 180 ℃,reaction time 3 h, raw material mass ratio of methyl eleostearate /acrylic acid 1:0.247 and the yield of TMAA was 85%.

MAA的最佳合成条件为:反应温度180℃,反应时间3 h,桐酸甲酯和丙烯酸的质量比为1:0.247,阻聚剂对苯二酚的加入量为丙烯酸质量的1%,产率为85%。

Thirdly,in the view of some different results between the reaction of complexes(2)、(3)and[(Me_3Si)_2N]_3LnLi_3 with aromatic aldehydes, the reaction of 2 equiv of aromatic aldehydes with 1 equiv of lithium amide(1) catalyzed by the YCl_3 was subsequently studied,and better yields of the corresponding amides and alcohols can be isolated.These results indicated that the enolate ligand in complexes(2)、(3)may have impact on the Cannizzaro disproportionation reaction.

第三,鉴于上述配合物2、3和[(Me_3Si_2)2_N]_3LnLi_3与芳香醛反应结果上的一些差别,我们又以三氯化钇为催化剂,将两当量的芳香醛与一当量化合物1的锂盐直接进行反应,结果以较好的产率得到了相应的酰胺和醇,这说明配合物2、3中所含的乙烯醇基可能对此Cannizzaro-型歧化反应存在一定的影响。

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