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When substrate molar ratio(ethyl caprylate/fish oil)15∶1 and 10% immobilized Lipozyme RM IM with added 30% water are mixed for 11 h at 45℃ SC-CO_2 and SC-CO_2 pressure 12.5 MPa,the interesterification activity of lipase is most effective and the highest incorporation of caprylic acid with triacylglycerol is obtained.

当反应温度为45℃,底物摩尔比为15∶1,酶用量为底物总量的10%,添加水量为酶量的30%,反应时间为11h,超临界CO2压力为12 5MPa时,脂肪酶LipozymeRMIM的催化效果最好,辛酸结合率在反应产物甘三酯中达最大值。

In this paper, grafting of crotonic acid, undecylenic acid, oleic acid, and acrylic acid onto acrylonitrile-butadiene-styrene terpolymer were studied. Experimental factors influencing grafting, kinetics and mechanism of grafting, the reactivity of grafted polymer, and the compatibilization effects of grafted ABS on ABS blends were investigated.

本文主要研究反式丁烯酸、10-十一烯酸、油酸、丙烯酸接枝ABS树脂的影响因素、接枝反应机理和动力学、接枝物的反应活性,以及接枝物对ABS共混物的增容作用。

The photocycloaddition of 1-naphthonitrile (1-NpCN) and 2,3-dimethyl-2-butene in cyclohexane or benzene gave cyclobutane 3 primarily,but that of 2-NpCN gave azetine 6 asthe major and cyclobutane 5 as the minor product in low conversion photolysis.

在低转化光解情况下,1-萘甲腈(1-NpCN)和2,3-二甲基丁烯-2在环已烷或苯中的光环加成反应主要得到环丁烷3,但2-NpCN主要得到氮杂环丁烯6和少量的环丁烷5,三氟醋酸量增加抑制1-NpCN和DMB的光环加成反应,表明TFA与基态及单激发态1-NpCN生成非光反应的复合物,它也淬灭(1-NpCN-DMB)激基复合物。

The photocycloaddn. of 1-naphthonitrile (1-NpCN) and 2,3-dimethyl-2-butene in cyclohexane or benzene gave cyclobutane I primarily, but that of 2-NpCN gave azetine II as the major and cyclobutane III as the minor product in low conversion photolysis. The photocycloaddn. of 1-NpCN with DMB is retarded by increasing amts. of trifluoroacetic acid which is shown to form non-photoreactive complexes with ground state as well as with singlet excited state 1-NpCN. It also quenches the *(1-NpCN-DMB) exciplex.

在低转光解情况下,1-萘甲腈(1-NpCN)和2,3-二甲基丁烯-2在环已烷或苯中的光环加成反应主要得到环丁烷3,但2-NpCN主要得到氨杂环丁烯6和少量的环丁烷5,三氟醋酸量增加抑制1-NpCN和DMB的光环加成反应,表明TFA与基态及单激发态1-NpCN生成非光反应的复合物,它也淬灭^*(1-NpCN-DMB)激基复合物。

To further extend the scope of this type Cannizzaro disproportionation reaction and the reactivity of enolate ligand in complex with aldehyde,we designed to synthesis new rare earth complexes containing arylamido and.enolate mixed ligands,studied their reactivity with aromatic aldehydes for the disproportionation reaction.

为了进一步探索这种歧化反应的应用范围及配合物中作为配体的乙烯醇基与醛的反应性,我们设计合成了含胺基、乙烯醇基混合配体的新型稀土配合物,并研究了其与芳香醛的反应。

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。

The results showed that the reaction activity between glycinin (7S subunit) and maltodextrin was high, and the reaction proceeds quantitatively regardless of the variation of protein and polysaccharide mass ratio. The molecular properties of the formed conjugates are also highly uniform. The reaction activity between β-conglycinin (11S subunit) and maltodextrin is relatively lower Compared to that of glycinin, and the molecular properties of these conjugates are affected by the variation of the R values.

电泳分析表明:7S亚基与麦芽糊精的反应性较高,而且在文中所研究的蛋白质与多糖质量比的范围内,7S亚基都能与麦芽糊精发生定量的共聚合反应,形成分子特性高度一致的共聚物;而11S亚基与麦芽糊精间的反应性较低,共聚物的分子特性受蛋白质与多糖质量比的影响。

The transesterification reaction among poly,poly(ethylene 2,6- naphthalate),and PET/PEN copolymer were studied with1H-NMR.

通过用1H-NMR对聚对苯二甲酸乙二酯与聚2,6-萘甲酸乙二酯、PET/PEN共聚物的共混物酯交换反应的研究,测得了反应速率常数、反应活化能和诱导期。

Photodissociation spectroscopy of the complexes Mg~+-NCSCH_3 Mg~+-S_2(CH_3_2 in the spectral region of 230-440nm was oberserved. As to Mg~+-NCSCH_3 of photo-induced reaction, there were three channels. And there are the products Mg~+ from nonreaction quenching and reactive products Mg~+NC, Mg~+NCS in the reaction throughout the whole wavelength range.

观察了复合物Mg~+-NCSCH_3Mg~+-S_2(CH_3_2在230~440nm范围的光解离光谱,在此波段内的复合物光诱导产物的质谱显示,对Mg~+-NCSCH_3:光诱导反应有三个通道,存在着非反应猝灭产物Mg~+和反应产物Mg~+NC、Mg~+NCS。

The infection of the reaction rate of the virous monomers was reviewed respectively by the different THF dosage, TMEDA dosage, t-BuOK dosage, t-AmOK dosage and different temperature. The monomers apparent reaction rate constant was obtained.And the polymer composition at different conversion was reviewed, too.The effect of modifier and temperature on heat effect was also studied. In addition, the sequence structure and microstructure of the terpolymer was reviewed at different modifier dosage, and the structure was characterized by the ~1H—NMR.

分别考察了不同THF、TMEDA、t-BuOK、t-AmOK加入量以及聚合温度对各单体及总的反应速率的影响规律,得到了各单体及总的表观反应速率常数,求得了不同转化率下各单体在共聚物中的分布情况,同时考察了调节剂加入量对聚合温升热效应的影响规律;研究了在三种聚合体系下,通过~1H—NMR对共聚物的结构进行了表征,分别考察了不同调节剂加入量对共聚物的序列结构及微观结构的影响规律。

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