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In 1997. Our company owns a fixed assets of 6 million RMB and a total area of 10,600 square meters. With powerful technical strength, it is the largest production base for r-chloropropyl, ethylene series silane coupler. And it is the member of China Organosilicon Association.

公司现有固定资产600多万元,占地面积10600平方米,科研技术力量雄厚,是全国较大的γ-氯丙基硅烷偶联剂、乙烯基硅烷偶联剂系列产品的生产基地,是中国有机硅协会认证的会员单位。

A steel bar is washed and dried, and then put into a glass pipe which is sealed to obtain stirring magneton; a mixed solvent of Gamma-methacrylate oxide propyl trimethoxy silane and methanol is prepared and added with an organic base to obtain a pre-bonding solvent; the stirring magneton is immerged into the pre-bounding solvent, and the outer surface of the glass pipe of the stirring magneton is bonded with a layer of silane substance with alkenyl; a reactive monomer mixture and a pore-forming agent mixed solvent are evenly mixed and then added into a container, the stirring magneton after the pre-bounding is put into the container which is sealed and then put into a water bath; after reaction, the container is removed, the stirring magneton coated with a polymer is taken out and put into a extractor and extracted by using a solvent; or the stir bar is immersed into the solvent till no impurity can be checked in the solvent, thereby obtaining the product.

将铁条清洗干燥,放入玻璃管内,密封得搅拌磁子;配制γ-甲基丙烯酸氧丙基三甲氧基硅烷与甲醇的混合溶液,加入有机碱得预键合溶液,将搅拌磁子浸入预键合溶液,在搅拌磁子的玻璃管外壁键合一层带烯基的硅烷化物质;将反应单体混合剂和致孔剂混合溶液混匀后倒入容器中,将预键合后的搅拌磁子放入容器,密封后置于水浴中,反应后除去容器,取出涂有聚合物的搅拌磁子,置于提取器中,以溶剂提取,或将搅拌棒置于溶剂中浸泡至溶剂中无杂质检出,得产物。

A self-assembled monolayer film of tolane was fabricated in aqueous solution by using silane coupling agent.

用硅烷偶联剂3-氨丙基-三乙氧基硅烷,通过自组装反应在石英基板表面制备了含有二苯乙炔基的自组装单层膜。

This paper is studied on a new synthesis method of amino-modified organic silicone micro-emulsion of cationic style by one step with a silane-alkyl coupling,3-(2-aminoethyl)-aminopropyl methyl dimethoxy silane while opening-cyclo polymerization of the octa-methyl cyclo tetra siloxane,thus the optimal manufacturing conditions are determined by comparing test of their properties.

采用硅烷偶联剂氨乙基氨丙基甲基二甲氧基硅烷改性,八甲基环四硅氧烷开环聚合,探索一步合成阳离子型氨基改性有机硅微乳新方法,通过其性能测试得出其最佳工艺条件:反应温度:80℃,反应时间:3 h,十六烷基三甲基溴化铵用量:5%,脂肪醇聚氧乙烯醚用量:5%,预乳液滴加时间:2 h。

The silica/Polystyrene monocore-shell nanocomposite particles(95nm in diameter) were synthesized through miniemulsion polymerization by using sodium dodecyl sulfate surfactant,hexadecane costabilizer in the presence of silica particles(50nm in diameter) coated with methacryloxytrimethoxysilane.

采用细乳液聚合法,以3-甲基丙烯酰氧基丙基三甲氧基硅烷(KH570)表面改性的直径50nm的氧化硅粒子为核,在乳化剂、助乳化剂、引发剂存在的情况下制备了小粒径、单核核壳结构氧化硅/聚苯乙烯纳米复合微球。

By using tetramethylammonium hydroxide as catalyst, a new silicone, amino and long-chain alkyl co-modified polysiloxanes was synthesized by bulk polymerization of octamethylcyclotetrasiloxane (D4), N-β-aminoethyl-γ-aminoproylmethyldimethoxysilane (YDH-602), dodecylmethyldimethoxysilane (HD-109) and hexamethyldisiloxane. The optimum experimental conditions were studied.

以八甲基环四硅氧烷(D4)、长链烷基甲基二甲氧基硅烷(HD-109)、N-β-氨乙基-γ-氨丙基甲基二甲氧基硅烷(YDH-602)和六甲基二硅氧烷为原料,在四甲基氢氧化铵催化下,采用本体聚合反应合成了一种新型硅油-氨基与长链烷基共改性硅油。

A quaternary surfactant, N,N-dimethyl-N-dodecylaminopropyltrimethoxy ammonium chloride was synthesized from γ-chloropropyl trimethoxy silane by quaterisation with N,N-dimethyldodecylamine.

利用γ-氯丙基三甲氧基硅烷与 N , N-二甲基十二烷基胺反应,合成了 N , N-二甲基-N-十二烷基氨丙基三甲氧基硅烷氯化铵。

Using tetrabutyl titanate and methyl methacrylateor 2-Hydroxyethylmethacrylate (HEMA as materials, methacryloxylpropyl trimethoxy siliane as coupling agent, HCl as catalyst, Poly-titania(PMMA-TiO2) nanocomposites and Poly-titania(PMMA-TiO2) nanocomposites were synthesized by sol-gel process.

以盐酸作为催化剂,将钛酸四丁酯水解制备二氧化钛(TiO2)溶胶;随后将所制备溶胶与甲基丙烯酸甲酯、硅烷偶联剂(γ-甲基丙烯酰氧丙基三甲氧基硅烷)相混合,以过氧化苯甲酰作为引发剂,经过聚合、缩合和溶胶-凝胶过程,制备了均匀透明的PMMA-TiO2纳米复合材料和PHEMA-TiO2纳米复合材料。

Tetraallylsilane was synthesized by one-step approach through the reaction of silicon tetrachloride with the partially solvated Grignard reagents formed in situ from allyl bromide and magnesium in the mixed solvents of toluene and ether.

采用一步合成方式,将3-溴丙烯与金属镁在以甲苯和供电子溶剂构成的混合溶剂中进行反应,继而与四氯化硅反应,成功合成了四烯丙基硅烷,其产率在乙醚与3-溴丙烯的摩尔比为4(V甲苯/V乙醚=1·1)时达到极值,超过了91%。

UV-curable hyperbranched poly was synthesized via organosilicon polymer bearing silicon hydride end groups and vinyltriallylsilane at the presence of Pt/C catalyst.

通过含硅氢键的超支化聚合物和乙烯基三烯丙基硅烷在铂催化剂作用下反应制备了可紫外光固化的超支化聚硅氧基硅烷。

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