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oxidation相关的网络例句

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The experimental results showed that, monochloroacetic acid and dichloroacetic acid enhanced photocatalytic hydrogen generation activity, but trichloroacetic acid did not improve it. The amount of produced H_2 increases almost proportionally to the irradiation time within 5 h irradiation. The photocatalytic oxidation of monochloroacetic acid and dichloroacetic acid mainly produced CO_2, HC1 and CH_2O, the photocatalytic oxidation of trichloroacetic acid mainly produced CO_2 and HCl.

实验表明,一氯乙酸、二氯乙酸的存在明显地提高了制氢反应效率,而三氯乙酸的存在却不能起到促进作用;反应5h内,反应生成氢的量与反应时间成线性关系;一氯乙酸、二氯乙酸光降解产物主要是CO_2、HCl和CH_2O,三氯乙酸光降解产物主要是CO_2和HCl;研究了溶液pH值对放氢反应的影响;在实验浓度范围内,一氯乙酸、二氯乙酸浓度对放氢反应的影响,表观上符合Langmuir-Hinshelwood关系式;考察了一氯乙酸、二氯乙酸在光催化剂表面的吸附。

Single ozone oxidation,single active carbon absorption and ozone oxidation-active carbon absorption technology were studied in order to discuss the practicability of removal of micro-content nitrobenzol in drinking water.

通过对O3氧化、活性炭吸附和O3氧化-活性炭吸附工艺的研究,探讨O3-活性炭工艺去除饮用水中少量硝基苯的可行性。

Department of Chemical Engineering, Chengde Petroleum College, Chengde, Hebei 067000, China)Single ozone oxidation, single active carbon absorption and ozone oxidation-active carbon absorption technology were studied in order to discuss the practicability of removal of micro-content nitrobenzol in drinking water.

承德石油高等专科学校化学工程系,河北承德067000 摘要:通过对0 氧化、活性炭吸附和0 氧化一活性炭吸附工艺的研究,探讨0 一活性炭工艺去除饮用水中少量硝基苯的可行性。

Results showed that single ozone oxidation can only remove about 50% nitrobenzol, single active carbon absorption can reduce nitrobenzol to a standard index mark when empty-bed station time exceeded 15 minutes, but ozone oxidation-active carbon absorption technology can remove nitrobenzol completely when the time exceeded 10 minutes.

研究发现:单独采用0 氧化能去除约50%的硝基苯;单独采用活性炭吸附,在空床停留时间大于15 min时可使出水指标达到标准要求;而对于O 氧化一活性炭吸附工艺,当停留时间在10 min 以上时,可完全去除水中的硝基苯。

It is found that NaOH exhibited significant cocatalytic action on the oxidation of o and p nitrotoluenes and had no cocatalytic action on the oxidation of m nitrotoluene, and the cocatalytic action of alkali NaOH increased as the concentrations of NaOH increased.

发现NaOH对氧气氧化邻、对硝基甲苯有明显的助催化作用,且碱的助催化作用随着NaOH浓度的增加而增加;而对氧气氧化间硝基甲苯则没有助催化作用。

Titania-supported nonprecious oxides catalysts have been prepared by impregnation and coprecipitation, respectively, and tested for carbon monoxide oxidation. The supported copper oxide catalyst showed higher catalytic activity for CO oxidation.

对浸渍法和共沉淀法制备得到的各种TiO2负载氧化物催化剂进行了活性组分的筛选,结果发现,两种方法得到的CuO催化剂均具有优良的CO氧化催化性能。

Recent developments of clean oxidation systems catalyzed by polyoxometalates are summarized in detail. The emphasis is on the epoxidation reaction of olefinic compounds, oxidation of alkanes and aromatic compounds with the comparatively ideal oxidants, hydrogen peroxide and molecular oxygen respectively.

文本总结了多金属氧酸盐在液相清洁催化氧化方面的进展,主要针对以过氧化氢和分子氧为氧化剂的烯烃类化合物的环氧化反应、烷烃和芳香族化合物的氧化反应,并详细探讨了此类氧化反应的反应机理。

It has been a difficult problem to figure out efficient methods in treating coking plant wastewater because the degradation is difficult. Homogeneous Fenton reagent is one of oxidation methods which applies H_2O_2 as oxidation and Fe~(2+) as catalyst. In reaction,·OH is one of free radicals with excellent oxidizability.

Fenton试剂法是一种采用过氧化氢为氧化剂、以亚铁盐为催化剂的均相催化氧化法,反应中产生的·OH是一种氧化能力很强的自由基,能氧化废水中有机物,从而降低废水的色度和COD值。

The optimum conditions were obtained as follows: the weight ratio of fatty acids and 85%acetic acid is 1:4, ozonolysis temperature is 20-25℃, manganese/copper acetate as catalyst, and the amount of catalyst is 0.15% of fatty acids, oxidation decomposition temperature and oxidation decomposition time are 90-95℃ and 4 hours respectively. the yields of azelaic acid and pelargonic acid are 57.4% and 51.6% respectively.

以菜油酸为原料、85%醋酸水溶液为溶剂,经臭氧化、氧化分解、重结晶等过程制备壬二酸和十三烷二酸的最佳反应条件为:m:m(85%醋酸)=1:4,臭氧化温度20-25℃;氧化分解温度80-85℃,催化剂醋酸锰/醋酸铜用量为原料菜油酸质量的0.12%,氧化分解时间3h,重结晶溶剂壬酸的用量为5倍质量的氧化分解产物时,十三烷二酸的收率为58.3%,壬二酸的收率为57.2%。

The smaller the electronegativity is, the higher oxidation activity is. Thus phosphomolybdic acid shows better catalytic oxidation activity than phosphotungstic acid.

由于磷钨酸中的钨可以脱出并少量沉积到催化剂表面,而且从电负性来说Mo-O的键能小于W-O,键能小的杂多酸有较强的氧化性,所以钼系杂多酸催化活性要好于钨系杂多酸。

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