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benzal相关的网络例句

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与 benzal 相关的网络例句 [注:此内容来源于网络,仅供参考]

The study on the technology and kinetics of chlorination of benzyl chloride is rather essential to the design of reactive distillation column in that the new technology about combination of reaction and distillation is used in the production of benzal chloride.

因为拟采用新型反应精馏耦合技术进行苄叉二氯的生产,研究氯化苄氯化工艺和动力学对于反应精馏塔的设计很有必要。

Using benzyl chloride and chlorine as starting materials, benzal chloride is prepared through photo-chlorination in loop reactor.

采用环流反应器、以氯化苄和氯气为原料进行光氯化反应,制备苄叉二氯;将制得的苄叉二氯粗品进行真空精馏得到高纯度的精品;然后用一种新型醇胺类相转移催化剂,分别以盐酸和水作为介质,在 90~ 110℃水解后得到了高纯度的苯甲醛。

By verifying the model, the value of model calculated coincided with the experiment value was obtained. hydrolysis ; benzal chloride ; phase transfer catalyst ; kinetic model

最近通用的方法是采用可溶性的金属锌盐(ZnCl2等)做水解催化剂,在此反应过程中,水的量对催化作用起着决定性的影响,必

The simplified peseudo-first-order kinetic model for hydrolyzation of benzal chloride was proposed according to the character of hydrolyzation reaction and the apparent reaction rate constant and activity energy was obtained. The activity energy is 17.73KJ/mol in the temperature range from 900C to 1100C and the model values and experimental values tally well.

根据水解反应的特点,提出了简化的苄叉二氯水解反应拟一级动力学模型,经参数估计,得出了水解反应的宏观反应速率常数和活化能,在900C~1100C温度范围内,反应活化能为E1=17.73kJ/mol,模型计算值与实验值吻合较好。

The procedure of benzal chloride and benzylchloride was obtained by chlorination toluene, then through catalytic acidic hydrolysis and oxidation, produced benzaldehyde.

本文研究了甲苯氯化得到苄叉二氯和氯化苄混合物,然后经催化酸解氧化制备苯甲醛,并探讨了氯化催化酸解及氧化的反应条件。

Substitutes on benzal benzene ring of BFP have different effects on .

BFP 苄基苯环上2-Cl、3-Cl、2-CH3、4-CH3、3-OCH3取代,可增强体外清除。

Substitutes on benzal benzene ring of BFP have different effects on ·OH scavenging activity in vitro. 2-Cl,3-Cl,2-CH3,4-CH3 and 3-OCH3 may enhance the activity. 3-CH3 may not change the activity.

BFP苄基苯环上2-Cl、3-Cl、2-CH3、4-CH3、3-OCH3取代,可增强体外清除·OH活性;3-CH3取代,体外清除·OH活性基本不变;2-OCH3、4-OCH3取代,体外清除·OH活性降低。

Substitutes on benzal benzene ring of BFP have different effects on ·OH scavenging activity in vitro. 2-Cl,3-Cl,2-CH3,4-CH3 and 3-OCH3 may enhance the activity. 3-CH3 may not change the activity. 2-OCH3 and 4-OCH3 may reduce the activity.

BFP苄基苯环上2-Cl、3-Cl、2-CH3、4-CH3、3-OCH3取代,可增强体外清除·OH活性;3-CH3取代,体外清除·OH活性基本不变;2-OCH3、4-OCH3取代,体外清除·OH活性降低。

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