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magnesium chloride相关的网络例句

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This paper presents the experimental data of metastable phase equilibrium of Na+, K+, Mg2+∥Cl-, SO2-4-H2O quinary system at 35 ℃, from which the metastable phase diagram is drawn. It consists of nine regions of crystallization saturated with sodium chloride, potassium chloride, glasserite(3K2SO4*Na2SO4), leonite(K2SO4*MgSO4*4H2O), kainite(KCl*MgSO4*2.75H2O), thenardite(Na2SO4), astrankit(MgSO4*Na2SO4*4H2O), carnallite(KCl* MgCl2*6H2O), magnesium sulfate hexahydrite(MgSO4*6H2O) and bischofit(MgCl2*6H2O).

研究得出(Na+, K+, Mg2+∥Cl-, SO2-4-H2O)五元体系35 ℃时的介稳溶解度数据,绘制了该体系35 ℃的介稳相图,共有9个为氯化钠所饱和的结晶区域:氯化钾、钾芒硝(3K2SO4*Na2SO4)、钾镁矾(K2SO4*MgSO4*4H2O)、钾盐镁矾(KCl*MgSO4*2.75H2O)、光卤石(KCl*MgCl2*6H2O)、白钠镁矾(Na2SO4*MgSO4*4H2O)、硫酸钠、六水硫酸镁(MgSO4*6H2O)和水氯镁石(MgCl2*6H2O)。

Using phosphoryl chloride as catalyst, 5,6-O-isopropylidene ascorbic acid was prepared by the reaction of Vc and acetone, then the product was treated with phosphoryl chloride to produce Magnesium L-ascorbate-2-phosphate.

在三氯氧磷催化剂作用下,Vc首先与丙酮反应生成5,6-O-异丙叉-L-抗坏血酸,再与三氯氧磷发生磷酰化反应合成得到。

Through the thermodynamic calculation of the reaction that aluminum and magnesium reduce anhydrous scandium chloride molten salt to prepare aluminium-magnesium-scandium master alloy, we got that the standard equilibrium constant of the reaction is 1.074 ×10~(19), and the experimental equilibrium constant of it is approximately 6.874 × 10~(14)under around 1200 K and 1 standard pressure, which demonstrate that the reaction can take place and proceed thoroughly.

通过铝镁热还原无水氯化钪熔盐制备铝镁钪中间合金反应的热力学计算,得出:在1200K左右温度,1标准大气压下,该反应的标准平衡常数K为1.074×10~(19),经验平衡常数K′约为6.874×10~(14),这说明铝镁热还原无水氯化钪熔盐法制备铝镁钪中间合金的反应能够进行,而且进行的很彻底。

The results of weight-loss tests of many magnesium alloys containing different concentration Al and Rare earth elements showed that the effect by only adding aluminum to improve the corrosion resistance of magnesium alloys in sodium chloride solution was unstable.

不同铝和稀土元素含量的镁合金的失重实验结果发现铝元素对于改善镁合金在NaCl溶液中耐腐蚀性能的作用是不稳定的。

Treating the crude monohydrate magnesium sulfate from the byproduct potassium chloride in the bittern chemical corporation,the process for the technical-grade heptahydrate magnesium sulfate is discussed,which results in increasing additional value and extending the application range of product.

针对苦卤化工企业副产氯化钾所得的粗一水硫酸镁产品,研究将其转化为工业级七水硫酸镁,增加产品附加值,扩大产品的应用范围。

Tetrachloroterephthalic acid was prepared by chlorinating terephthalic acid, oleumsolvent and iodine catalyst. Tetrachloroterephthalic acid was acylated by sulphurous oxychloride in the presence of DMF to form tetrachloroterephthaloyl chloride. The acyl chloride product was fluorinated by potassium fluoride and esterified by methanol to synthesize dimethyl tetrafluoroterephthalate. The ester was reduced with potassium borohydride and lithium chloride to give tetrafluoroterephthalyl alcohol. The above product was bromated in the hydrobromic acid to obtain 4-bromomethyl-2,3,5,6-tetrafluoro-benzene methanol. 4-Methyl-2,3,5,-6-tetrafluorobenzene ethanol was obtained by reducing the bromide with magnesium. In the exist of DCC and DMAP, tefluthrin was got by the condensation reaction between 4-methyl-2,3,5,6-tetrafluoro-benzene methanol and-(1RS,3RS)- 3-(2- chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethyl cycolpropanecar-boxylate acid.

对苯二甲酸与氯气在碘存在下以发烟硫酸为溶剂进行氯化制备四氯对苯二甲酸;再以DMF为催化剂与二氯亚砜反应生成四氯对苯二甲酰氯;以氟化钾为氟化剂,环丁砜为溶剂置换氟化,再与甲醇酯化得到四氟对苯二甲酸甲酯;以KBH4-LiCl为还原剂二甲醚为溶剂反应制得四氟对苯二甲基苄醇;以氯苯为溶剂在溴化氢溶液中溴化得到溴化产物;在乙醇溶液中经镁粉还原得到4-甲基-2,3,5,6-四氟苄醇;甲基苄醇与功夫酸在催化剂二环己基碳二亚胺和4-二甲氨基吡啶作用下缩合得到七氟菊酯,总收率达43.6%。

High temperature or isobutyl aluminum pre-treated magnesium chloride was unfavorable for increase of the catalytic activity.

高温及使用异丁基铝预处理氯化镁均不利于提高催化活性,振动球磨较滚动球磨有利于提高催化活性,高活性催化剂的制备时间应大于15h。

Methods 4-Hydroxy- benzonitrile was treated with sodium hydrogen sulfide and anhydrous magnesium chloride in dimethyl formamide to give thioamide, which was then directly cyclized with ethyl 2-chloroacetoacetate without separation to give ethyl 2-(4-hydroxyphenyl)-4-methylthiazole-5-carboxylate(2) in one-pot; then 2 was formylated with Duff reaction adopting hexamethylenetetramine in trifluoroacetic acid to give ethyl 2-(3-formyl-4-hydroxyphenyl)-4-methylthiazole-5-carboxylate(3); finally, the target compound was obtained by the treatment of 3 with hydroxylamine hydrochloride and sodium formate in formic acid.

采用&一勺烩&方法,以4-羟基苯甲腈为起始原料,首先与硫氢化钠和无水氯化镁在N,N-二甲基甲酰胺中反应,所得中间体不经分离,直接加入2-氯乙酰乙酸乙酯进行环合反应,得到2-(4-羟基)苯基-4-甲基-5-噻唑甲酸乙酯(2);然后通过六亚甲基四胺/三氟乙酸进行Duff反应,得到2-(3-甲酰基-4-羟基)苯基-4-甲基-5-噻唑甲酸乙酯(3);再经盐酸羟胺/甲酸/甲酸钠体系脱水得到目标化合物。

Computation makes clear as a result, the smooth balance of power that 6 ammonia in 6 ammonia magnesium chloride form in nucleus and other electron breaks up in field, cent is two class, the first class 4 ammonia, the 2nd class 2 ammonia, when outside ambient changes, it is to shuck off 4 ammonia element likely most, additionally 2 ammonia are shucked off again after warming up, this one conclusion accords with experimental result to agree.

计算结果表明,六氨氯化镁中的6个氨在原子核和其它电子形成的平均势场中分裂,分为两级,第一级4个氨,第二级2个氨,当外界条件变化时,最有可能是脱去4个氨分子,升温后再脱去另外2个氨,这一结论符合实验结果一致。

Light calcium carbonate, ACC, nanometer superfine calcium carbonate, magnesium carbonate, trihydrate alumina, silica white, strontium carbonate, barium carbonate, potassium carbonate, rubberlith, rongalite, permanent white, lemery, microspheroidal catalyst, magnesium hydrate, bluestone, nickel salt, sodium molybdate, sodium chloride, potassium chloride, calcium chloride, sodium fluoride, cryolite, iron oxide red, lithium hydroxide, zirconium hydroxide, calcium phosphate, sulfur, etc.

轻质碳酸钙、活性碳酸钙、纳米级超细碳酸钙、碳酸镁、氢氧化铝、白炭黑、碳酸锶、碳酸钡、碳酸钾、立德粉、保险粉、硫酸钡、硫酸钾、微球催化剂、氢氧化镁、硫酸铜、硫酸镍、镍酸铵、钼酸钠、氯化钠、氯化钾、氯化钙、氟化钠、冰晶石、氧化铁红、氢氧化锂、氢氧化镍、氢氧化锆、磷酸钙、硫磺等。

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