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We also developed this extracting method for NO detection in aqueous phase by using another organic solvent butanol.

我们还以正丁醇为溶剂,进一步发展了这种有机溶剂提取的方法,使之适用于水相中NO的检测。

In the system,cetyltrimethylammonium bromide was used as surfactant,octane was used as solvent and butanol was used as co-solvent.

在反胶束体系中采用十六烷基三甲基溴化铵作为表面活性剂,正辛烷和丁醇作为溶剂及助溶剂

In the dilution of the solvents, additional polar solvent such as butanone, isopropyl alcohol, ethanol, and so on to ethhyl.

在不浓缩的溶剂洋,补增极性溶剂,如丁酮、异丙醇、乙醇等,多用乙酯。

Outlined solvents like, butanone ethyl acetate, acetone, methybenzene ethanol are quick drying solvents.

以上列举的溶剂中象醋酸乙酯、丁酮、丙酮、甲苯、乙醇都属快干溶剂

Resin and rubber used as the solvent, to dissolve polystyrene, ABS, PMMA, polyvinyl butyral, polysulfone, polyether chloride, styrene butadiene rubber, solvent-based adhesive preparation

用作树脂和橡胶的溶剂,能溶解聚苯乙烯、ABS、聚甲基丙烯酸甲酯、聚乙烯醇缩丁醛、聚砜、氯化聚醚、丁苯橡胶等,配制溶剂型胶粘剂

By studying the membrane preparation process for the typical membrane materials of polystyrene and cellulose acetate as well as a new type membrane material of polyvinyl butyral,the effects of operating parameters on the membranes structure are determined.By the study on the thermodynamics involved in the ternary systerms of ScCO_2/solvent/polymer and the calculation of theoretical ternary phase diagrams,the phase demixing behavior during the membranes formation by ScCO_2 induced phase separation process are described.By studying thermodynamics involved in the quaternary systerms of ScCO_2/solvent/additive/polymer,the effect of a low molecular weight additive on the quaternary phase diagram and dimixing speed are revealed.

通过对传统膜材料聚苯乙烯、醋酸纤维素及新型膜材料聚乙烯醇缩丁醛进行ScCO_2诱导相转化制膜工艺的实验研究,给出了操作参数对膜形态结构的影响规律;通过研究ScCO_2/溶剂/聚合物三元体系热力学问题,并计算出相应铸膜体系的三元相图,对ScCO_2诱导相转化膜制备过程的分相成膜行为进行了分析与描述;通过研究ScCO_2/溶剂/小分子添加剂/聚合物四元铸膜体系的热力学问题,并借助于四元体系理论相图计算的结果,分析了小分子添加剂对相分离过程的影响。

The microparticles were prepared by the solvent/non-solvent method, using biodegradable poly-3-hydroxybutyrate PHB as the scaffold to capsulate the 5-Fu.

为降低该类药物的释放速度,首先利用溶剂溶剂法,以生物可降解的聚羟基丁酸酯为骨架,制备了抗癌药物5-氟尿嘧啶的微粒。

Therefore, when configuration resolver leather lustre-coating agent uses the alkyd resin and the melamine xylenol-formaldehyde resin and the cellulose nitrate mix method, the retention cellulose nitrate Cheng Mo merit, improves it not to bear the aging, the cold resistant bad shortcoming, undergoes the repeated test, compounds the successful resolver lustre-coating agent to have the very good radiance and softness, bears the stretch, bears scours, becomes the membrane to be smooth.

因此,在配制溶剂型皮革光亮剂时采用醇酸树脂和三聚氰胺甲醛树脂与硝化纤维混合的方法,保留硝化纤维成膜的优点,改进其不耐老化,耐寒性较差的缺点,经过反复试验,配制成功的溶剂型光亮剂有很好的光亮度及柔软度,耐拉伸,耐擦洗,成膜光滑。

The invention discloses an InP quantum point preparing method, comprising the steps of:(1) mixing InCl3 with trioctylphosphine oxide, and preserving heat at 90-110DEG C to prepare a solution whose In content is 0.1-0.3mol/L;(2) raising temperature to 130-180DEG C, and charging argon gas;(3) injecting PSi(CH333 into InCl3-TOPO compound in the molar ratio of 1 to 1-1 to 2;(4) when the solution color turns into transparent red or orange, raising temperature to 260-270DEG C and preserving heat;(5) lowering temperature to 90-110DEG C and injecting dodecyl amine, decyl amine or mercaptan;(6) dissolving reacting mixture in nonpolar solvent to form transparent colloidal solution, then adding in polar solution until the colloidal solution is muddy, and centrifugally separating and obtaining deposits and supernatant; and (7) centrifugally separating the supernatant, where the above steps (1)-(5) are performed.

本发明公开了一种InP量子点的制备方法,其步骤为:①将InCl 3 与三辛基氧膦混合,在90~110℃保温制得In含量为0.1~0.3mol/L的溶液;②升温到130~180℃,通入氩气;③将PSi(CH 3 3 3 注射入InCl 3 -TOPO复合物中,其摩尔比为1∶1~1∶2;④待溶液颜色变为透明的红色或橙红色,将升温260~270℃保温;⑤降温到90~110℃,注入十二胺、癸胺或硫醇;⑥将反应混合物溶于非极性溶剂,形成透明的胶体溶液,然后加入极性溶剂,直至胶体溶液出现混浊状,然后离心分离获得沉积物和上层清液;⑦取上层清液进行离心分离。上述步骤①~⑤在保护气氛下进行。

In addition, the devices with optimizing the mixture of chloroform and cyclohexanone, and mixture of chloroform and chlorobenzene showed a current efficiency as 0.468 and 0.816 cd/A, respectively.

另外,本实验中氯仿和环己酮混合溶剂的最佳电流亮度效率为0.468 cd/A,氯仿和氯苯混合溶剂的0.816 cd/A。

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