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potassium acid carbonate相关的网络例句

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Preparation of the cathode includes:shaping under the press of 40Mpa, sintering at 550℃for 1 hour and at 900℃for 8 hours and threading with molybdenum bar; Considering the literatures we choose CaCl2 as salt for preparation titanium. Pretreatment of salt is for 1 hour at 100℃and for 2 hours at 300℃. Partial pressure of oxygen which need lower than 5.11×10-7Pa to reduct titanium oxides and hygroscopic property of salt need a sealed equipment to electrolyse. And finally successfully designed a satisfied one and the results show that the equipment can be satisfied the requirment of the experiment. Flow of the inert gas is 1.5L/min, the voltage is 2.8 V, temperature is 850℃and time is 2 hours during pre-electrolysis. Flow of the inert gas is 0.2L/min, the voltage is 3.1 V, temperature is 900℃and time changes with the mass of TiO2 during electrolysis, namely the greater need the longer time; To eliminate influence of salt and other impurities, the products need to wash with distilled water and dilute chlorhydric acid , then wash with dilute hydrochloric acid under supersonic wave assistant. Finally, electrometical properties of the electrolysis of TiO2 is researched by cyclic voltammetry and chronoamperometry, and results show that there are two main reodox steps, namely from TiO2 to TiO and from TiO to Ti.

阴极制备主要包括40MPa压力下模压成型、两段式烧结(1小时内升至550℃保温1小时,再1小时升温至900℃保温8小时)及烧结后TiO2块打孔用钼棒串接三个主要环节;实验中选用CaCl2作为电解熔盐,并对其进行预处理(100℃,保温1小时; 300℃,保温2小时);经热力学计算,还原钛氧化物的氧分压至少要低于5.11×10-7Pa,结合电解过程中所用熔盐CaCl2有极强的吸水性的特点,电解装置应有较高的密封性,自行设计了一套密封性可靠的电解装置,便于实验过程中熔盐预处理和氧分压的控制;通过干燥处理预电解过程中Ar流量大约为1.5L/min、电压为2.8 V、温度为850℃、时间为2小时,电解过程中Ar流量大约为0.2L/min、电压为3.1V、温度为900℃,实验结果表明电解时间与TiO2质量密切相关,质量越大需要电解的时间越长;通过自来水冲洗—稀盐酸浸泡、洗涤—在超声波辅助作用下稀盐酸洗涤,可减少熔盐及其它杂质对电解产物检测结果的影响;最后,通过循环伏安法、计时电流法对电解机理的研究,确定电解还原TiO2制备金属钛主要经历了TiO2-TiO-Ti的过程。

Activation with dilute chloric acid or sulfuric acid solution was adopted as pretreatment of traditional citric gold plating .

传统的柠檬酸盐镀金工艺前处理采用稀盐酸或稀硫酸活化,活化液可能被带入镀金溶液,造成SO2-4、Cl-积累,严重影响柠檬酸镀金溶液的稳定性和镀层质量。

The result of chemistry show-colour analysis shows ,β―sitosterol extract was soluted in chloroform , and add vitriol , the interface of double liquid layer showed rose colour .β―sitosterol extract was soluted in acetic acid and add three chloridize iron--acetic acid—vitriol solution , it showed blue , then became pansy .

显色反应的结果显示,β―谷甾醇提取物于氯仿和浓硫酸反应后呈现玫瑰红色,与三氯化铁-乙酸-浓硫酸溶液反应后呈现蓝色,再变为紫罗兰色。

The mechanism for chlorinate acetic acid to monochloroacetic acid by using acetic anhydride or sulfur as catalysts respectively was studied.

通过对硫磺和乙酐催化氯化制备氯乙酸反应机理的分析研究,采用硫磺及乙酐复合催化剂,并且对氯化温度、氯化气氛、尾气回收等进行了过程优化,实现了乙酸氯化反应工艺条件的重大突破,使得氯乙酸的收率达到92.1%。

The optimum synthetic conditions of ethyl chloroacetate are: molar ratio of chloroacetic acid to ethanol is 1:8, the quantity of catalyst[Fe2(SO4)3 xH2O] is 10% of the mass of chloroacetic acid, reaction time is 1 hour, 5A zeolite was used as dehydrating agent. In these conditions, the yield of ethyl chloroacetate was up to 73%.

用Fe_2(SO_4)_3·xH_2O作为催化剂合成氯乙酸乙酯的较佳反应条件是:酸醇物质的量之比为1:8,催化剂用量为氯乙酸质量的10%,以5A分子筛作为脱水剂,回流时间1h,收率达73%以上。

Annual production: 10,000 tons of chloroacetic acid, amino acid 8000 tons, 35,000 tons hydrochloride.

公司年生产:氯乙酸10000吨、氨基乙酸8000吨、盐酸35000吨。

After pioneering the development of recent years has become a larger national, Henan The largest amino acid, chloroacetic acid production base.

经过近几年的创业发展,已成为全国较大、河南最大的氨基乙酸、氯乙酸生产基地。

The article introduced that α-Naphthaleneacitic acid was synthesized from naphthalene and chloroacetic acid in presence of aluminium powder.

介绍了萘和氯乙酸在铝粉催化下合成α—萘乙酸的研究。

The use of chemically-methyl phenol and chloroacetic acid to synthesize methyl-phenoxyacetic acid.

利用化学方法将间甲基苯酚和氯乙酸合成为间甲基苯氧乙酸。

Naphthoxyacetic acid was synthesized from 2-naphthol , sodium hydroxide and chloroacetic acid under the microwave radiation.

在微波辐射下,以2-萘酚、氢氧化钠和氯乙酸为原料合成了2-萘氧乙酸。

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