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The resultedα-methylamine was protected by acetyl chloride, and then was chlorosulfonated bychlorosulforic acid at -5℃-0℃followed by treatment with aqueous ammonia givingcompound A in 52.3% yield.

甲基胺再用乙酰基进行保护后,以HSO3Cl为试剂进行氯磺化反应,再用浓氨水进行反应,制得了乙酰基保护的苯磺酰胺类化合物。

The products include antioxidants,blowing agents,organic solvents, intermediates for pesticides,drugs and dyestuffs,perfumes,water glass,silicates,molybdenum compounds,graphite series,activated carbon,plasticizers,flame retardant,heat stabilizers,food additives and chemical reagents,etc.

注册商标有&鹿牌&合成樟脑,&桃浦&牌合成樟脑副产物和其他化工产品,&金牛&牌抗氧剂,发泡剂,水合肼,二甲基乙酰胺,二甲基乙醇胺,&海球&牌硅胶系列,&飞铃&牌磷氯,双乙烯酮衍生物,磷酸酯,乙烯利等,&泉字&牌,&水晶&牌各类泡化碱系列,&上胶&牌钼类化合物,石墨类产品系列。

Two new methods about preparation of nano-inorganic coated polymer microsphere have been found. The research mainly focused on controlled precipitation of inorganic precurdors onto the polymer microspheres, technique of preparation and size distribution of transition metal oxides and sulfides emulsion particles, nano-paticles''surface modification and the HLB values adjustment, emulsification of oil-soluble monomer in inorganic colloid and emulsion stability, emulsion polymerization that inorganic particles act as medi-phase, the preparation of inorganic nano-particle/polymer hybrid microspheres, preparation of hybrid materials in inverse emulsion, inverse emulsion polymerization of acrylamide and its phase behavior. Inorganic nano-particles we studied concerning TiO2、SiO2、Fe3O4、ZnO、ZnS、Ag and black carbon. Also we studied the morphology and capability of the hybrid materials.

主要内容有:无机物在高分子乳胶模板体系的界面定位沉积研究;过渡金属氧化物、硫化物纳米胶体粒子的制备工艺与胶粒尺寸分布研究;纳米粒子的表面修饰及其亲水亲油平衡值的调制;油溶性单体在无机胶体中的乳化行为与乳液稳定性研究;以无机纳米粒子做中介相的乳液聚合与无机纳米粒子/高分子复合微球制备研究;反相体系中杂化材料的制备;丙烯酰胺水溶液反相乳液聚合、相行为与稳定性;丙烯酰胺反相体系中无机粒子的制备研究;涉及到TiO2、SiO2、Fe3O4、ZnO、ZnS、Ag、碳黑等纳米无机物,系统考察了相关材料的形态与性能,为其应用开发奠定了基础。

The pKa values of the amide nitrogen atom are calculated at various hybridization states in amides.

在酰胺中,计算了不同杂化状态时,酰胺氮原子的不同pKa值。

For the first time,our group found that lanthanide amides can initiate the Cannizarro disproportionation reaction of aromatic aldehydes.

我们小组首次发现了通过稀土胺基化合物引发芳香醛发生Cannizzaro-型歧化反应,生成相应的酰胺和醇。

Thermal imidization of the polyamic acid derived from BPADA and BAPS was investigated mainly by GPC and FTIR equipped with an in-situ hot cell.

利用GPC、原位FTIR测定了长链聚酰胺酸PAA由双酚A二酐与 4 ,4′-二(4-胺基苯氧基二苯酚制备的热环化过程。

Based on the experimental results, it could be consequentially concluded that N-methoxycarbonylation of aromatic amines was followed by the exclusive N-methylation of methyl N-aryl carbamates during the reaction process.

苯环上有钝化基团的一级芳胺反应活性比较好,获得N-甲基-N-芳基氨基甲酸甲酯的产率较高,反应时间也较短;而苯环上活化基团的存在,则会降低一级芳胺的反应活性。

The SmI2-mediated reductions of ketones,imines and α,β-unsaturated esters have been shown to be instantaneous in the presence of H2O,an amine and in THF.

在水、胺以及四氢呋喃存在下二碘化钐参与的还原酮、亚胺以及α,β不饱和酯的反应能够在瞬间完成。

The complexes areneutral as shown by values of molar conductivity in aqueous solution, namely,〓 The crystal structure determinations show that, in complexes, metal ions werecoordinated by four nitrogen atoms and form slightly distorted square planar configuration,relationship between fluorene ring plane and coordination plane is similar to those betweenpeptide planes of β-folding in proteins. The complex molecules linked by hydrogen bonds formone dimension chain or two dimension network structure.

摩尔电导测定表明他们都是二氧四胺中酰胺氮去质子化后形成的产物。X-射线衍射晶体结构测定表明〓的铜、镍配合物的配位多面体都是稍微畸变的平面正方形,配合物分子中芴基平面与配位平面的关系类似于蛋白质β-折叠结构中肽平面之间的关系,配合物分子之间通过氢键连接成一维链状或二维网状结构。

In this research, liposoluble chlorogenic laurate was synthesized by the acylation with lauroy chloride in the existence of alkali catalyst in non-water phase, and yellowish CGL powders with a yield of 81.24% were obtained under the optimal synthesis conditions determined via single-factor tests and orthogonal experiments, that is, carrying out the acylation at 35℃ for 8h with a n:n: n ratio of 1:1:1.5 and with dimethylformamide as the solvating agent and the thinner.

文中对绿原酸进行了改性,即在碱性催化剂催化的条件下使其与月桂酰氯进行非水相的酯化反应,得到了脂溶性的绿原酸月桂酸酯。经过单因素及正交试验,确定了最佳合成条件为:以N,N-二甲基甲酰胺作为溶解、稀释剂,绿原酸/月桂酰氯/三乙胺的摩尔比为1:1:1.5,温度控制在35℃,反应时间8h。

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