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环己醇

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Sodium cyclohexanoloxyacetate was synthesized by 1mol︰1.15mol of cyclohexyl sodium alcoholate to sodium chloroacetate at 135145℃.The reaction time was 2.5h and the yield was about 81%.The sodium cyclohexanoloxyacetate was acidified by HCl to get the intermediate product,2-cyclohexanoloxyacetic acid.

以摩尔比为1︰1.15的环己醇钠和氯乙酸钠为原料,在135145℃下反应合成了环己氧基乙酸钠,反应时间为2.5h,收率约为81%,再将环己氧基乙酸钠用盐酸酸化制得中间体环己氧基乙酸。

In the condition of 1 MPa O_2 and 413 K for 4 h, the conversion of cyclohexane is 16.9%, and the total selectivity of cyclohexanol and cyclohexanone is 93%.

在该反应条件下,环己烷的转化率为16.9%,环己酮和环己醇的总选择性为93%。

The major products were cyclohexanecarboxylic acid and cyclohexanol. The possible reaction pathway was similar to that of benzene.

这一体系也可用于环己烷的羰基化反应,产物为环己甲酸和环己醇,反应历程与苯羰基化基本相同。

The catalytic oxidation of cyclohexane to cyclohexanone and cyclohexanol in air as probe reaction was performed without any organic solvent or cocatalyst, and the influences of the amount of metal porphyrin, reaction pressure, reaction temperature and reaction time on the catalytic activity were investigated.

以空气氧化环己烷制备环己酮和环己醇为探针反应,在不加入任何有机溶剂或助催化剂的条件下考察了金属卟啉用量、反应压力、温度、时间等对其催化活性的影响。

Effects of various parameters such as potential scan rate and cyclohexanol concentration on the eletro-oxidation of cyclohexanol were also studied.

初步认为,NiO首先被氧化为NiOOH,NiOOH再与环己醇发生还原反应生成己二酸和NiO,因此,NiOOH可作为较好的催化环己醇氧化反应的催化剂。

It was found that manganese porphyrin had the highest activity, and a maximum 15.4% of cyclohexane conversion and 93.9% selectivity of cyclohexanone and cyclohexanol could be obtained under the suitable conditions.

结果发现,锰卟啉催化活性最好,在适宜反应条件下,环己烷转化率高达15.4%,环己酮和环己醇的总选择性约为93.9%。

The commercial processes of cyclohexane oxidation to cyclohexanone and cyclohexanol generally show many problems, such as low conversion, poor selectivity, complicated technology, high-energy consumption and environmental pollution. So it seems to be of great academic and practical interesting to study and develop highly efficient and environmentally friendly catalytic cyclohexane oxidation processes.

现有的环己烷氧化制环己酮和环己醇生产工艺普遍存在转化率低、选择性差、工艺复杂、耗能大和对环境污染严重等问题,这就使得研究和开发高效、环境友好的环己烷催化氧化工艺具有重要的理论意义和实用价值。

The result of situ-FTIR study on the process of dehydrogenation of CHL, we concluded the reaction mechanism, and proved that monovalence copper had more activity than zero valence copper and the side reaction mainly took place on zero valence copper.

通过对环己醇脱氢反应过程的原位傅立叶变换红外光谱研究,推导出了反应机理,得出Cu〓较Cu〓更具有环己醇脱氢活性,环己醇脱氢的副反应主要发生在Cu〓上。

The catalytic activity of iodine in the esterification reaction was studied by synthesis cyclohexyl acetate from acetic anhydride,cyclohexano and acetic acid,cyclohexano.

以单质碘为催化剂,通过乙酸酐、环己醇及乙酸、环己醇为原料合成乙酸环己酯,对碘的催化活性进行了研究。

Using cyclohexanol as raw material, in presence of sodium tungstate and phosphotungstic acid as catalyst, the technique for oxidizing cyclohexanol to cyclohexanone with hydrogen peroxide were discussed.

环己醇为原料、钨酸钠和磷钨酸配合为催化剂,探讨了双氧水为氧化剂氧化环己醇合成环己酮的工艺方法。

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