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苯酰胺

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Acenaphthene was dehydrogenated to afford acenaphthylene by photochemical reaction with N bromosuccinimide in benzene with the addition of quinoline at room temperature and atmospheric pressure was studied.

在常温常压下,以苯作为溶剂,加入喹啉,使苊与N-溴代丁二酰亚胺发生光化学脱氢反应生成苊烯。

High molecular weight polymer Ⅰ and Ⅱ with decomposition temperature of 560℃ were prepared from condensation of two diamine and terephthaloyl chloride respectively.

两种二胺分别与对苯二甲酰氯进行直接缩聚反应,得到的聚合物分别为缩聚物Ⅰ和Ⅱ,两种缩聚物的热分解温度均超过560℃。

Purified water, euphorbia cerifera wax, glyceryl stearate, ammonium acrylates copolymer, butylene glycol, copernica cerifera wax, stearic acid, sucrose acetate isobutyrate, acrylates copolymer, bentonite, tromethamine, hexylene glycol, silk amino acids, cholesterol, glycine, synthetic wax, ethylhexyl glycerin, alanine, PEG-9 dimethicone, nylon-6, lecithin, silica, simethicone, caprylyl glycol, xanthan gum, propylene glycol, isostearic acid, sodium laureth-12 slfate, ceteareth-20, polyvinyl alcohol, sodium chloride, sodium acetate, disodium EDTA, benzyl alcohol, chlorphenesin, phenoxyethanol, methylparaben, ethylparaben, propylparaben, butylparaben, isobutylparaben, may contain /- mica, iron oxides (CI 77491, CI 77492, CI 77499), titanium dioxide (CI 77891), ferric ferrocyanide (CI 77150), ultramarines (CI 77007), blue 1 lake (CI 42090), bronze powder (CI 77400), aluminum powder (CI 77000), bismuth oxychloride (CI 77163), carmine (CI 75740), chromium hydroxide green (CI 77289), chromium oxide greens (CI 77288), yellow 5 lake CI 19140

水,小烛树蜡,硬脂酸甘油酯,丙烯酸铵共聚物,1,3-丁二醇,巴西棕榈蜡,硬脂酸,异丁酸醋酸蔗糖酯,丙烯酸酯共聚物,蒙脱土,二吡喃乙酸乙酯胺,已烯醇,丝氨酸,胆固醇,甘油,合成蜡,异丁基甘油,丙胺酸,PEG-9二甲基硅油,尼龙-6,卵磷酯,硅粉,硅氧烷,癸酰基乙二醇,汉生胶,丙二醇,异硬脂酸,月桂基醚-12硫酸钠,十六十八醇醚-20,聚乙烯醇,氯化钠,醋酸钠,EDTA二钠,苯氧乙醇,氯代苯酚,卞醇,尼泊金甲酯,尼泊金乙酯,尼泊金丙酯,尼泊金丁酯,尼泊金异丁酯,[可能还含有云母,铁黑(CI 77491, CI 77492, CI 77499),钛白粉(CI 77891),氰化亚铁(CI 77150),靛蓝(CI 77007),蓝1号(CI 42090),青铜粉(CI 77400),铝粉(CI 77000),氯氧化铋(CI 77163),洋红色素(CI 75740),氢氧化铬绿(CI 77289),氧化铬绿(CI 77288),黄5号(CI 19140)]文章来自网络,不代表本网站立场,版权归原作者所有,转载请注明出处!

Based on this monomer, several novel polyimides bearing side chain s composed of cyano-biphenyl mesogenic end groups and hexylene spacer were prepared.

合成了一种含氰基联苯氧基侧链的二元胺单体,然后通过两步法热酰亚胺化工艺制备了新型的含氰基联苯基团侧链的聚酰亚胺。

N,N '- ditertbutyl nitroxyl radical, 2, 2,6,6- tetramethyl-4 - hydroxyl piperdinehy droxylamine and its nitroxyl radical, as inhibitors of the BPO- initiated copolymerization of styrene (M 1 ) with acrylonitrile (M2 ), at 60℃,has been studied.

研究了二叔丁基羟胺,二叔丁基氮氧自由基,2,2,6,6-四甲基-4-羟基哌啶羟胺和2,2,6,6-四甲基-4-羟基哌啶-1-氧自由基对过氧化苯甲酰60℃引发的苯乙烯(M1)-丙烯腈(M2)共聚合的阻聚行为。

Mainly engaged in sodium azide, barium azide, three phosphorus nitride Friday, phenyl isothiocyanate, 1 - phenyl -5 - mercapto-tetrazole, 4 - dimethylamino-pyridine, 2 - mercapto--5 -- methyl-1,3,4 thiadiazole, N-hydroxy phthalimide, anhydrous betaine and betaine hydrochloride, such as fine chemical raw materials and medicine, pesticide intermediates of the development, production and sales.

主要从事叠氮化钠,叠氮化钡,五氮化三磷,异硫氰酸苯酯,1-苯基-5-巯基四氮唑,4-二甲氨基吡啶,2-巯基-5-甲基-1,3,4噻二唑,N-羟基邻苯二甲酰亚胺,无水甜菜碱及甜菜碱盐酸盐等精细化工原料及医药、农药中间体的开发、生产和销售。

Triphosgene ; carbamic acid ethyl ester ; phthalimide

三光气;胺基甲酸乙酯;邻苯二甲酰亚胺

With the in-situ single-stage self-metallization protocol,surface-silvered polyimide film has been prepared using pyromellitic dianhydride/ 4,4\'-oxydianiline-based polyimide as the matrix and (1,1,1-trifluoro-2,4-pentadionato)silveras the silver precursor.

在原位一步自金属化法中,以均苯四甲酸酐/4,4\'-二胺基二苯醚基聚酰亚胺为基体,以三氟乙酰丙酮银作为银的母体制备出了表面金属化的聚酰亚胺银复合薄膜。

Model compounds were synthesized from benzoyl chloride and diamine Ⅰ or diamine Ⅱ in NMP with anhydrous lithium chloride. Structures of model compounds were measured by melting point, FT-IR, element analysis and 〓H NMR. Reaction mechanism was from model reaction.

二胺Ⅰ和二胺Ⅱ分别与苯甲酰氯在含有LiCl的NMP溶液中合成模型化合物,采用熔点,FT-IR,元素分析,〓H NMR等方法对模型化合物的结构进行了表征,根据模型反应确定反应机理。

Seven biogenic amines were extracted from a sample with 6% perchloric acid, then derivatized with benzoyl chloride. 0.02 mol/L borate buffer (pH 9.2) containing 0.06 mol/L sodium deoxycholate-methanol (95∶5, v/v)was used as a running buffer. The detection wavelength was set at 214 nm. The separation was achieved within 12 min. Good linearities were observed from the calibration plots in the concentration ranges.

样品经6%过氯酸萃取后,由苯甲酰氯衍生化,以含0.06 mol/L脱氧胆酸钠的0.02 mol/L硼酸(pH 9.2)-甲醇(体积比为95∶5)混合液为电泳介质,电泳电压25 kV,温度25 ℃,检测波长214 nm,在12 min内实现了7种生物胺的完全分离。7种生物胺的浓度与其峰面积在一定的范围呈良好的线性关系,检出限除组胺为15 μg/g外,其余均为5 μg/g。

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