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In this paper the emulsion of polyacrylamide was synthesized in the polyglycol solutions, acryl amide and acrylic acid sodium was used as the monomer. In more detail, we investigated the effect of the concentration of the monomers, the ratio of monomer and PEG, the ratio of monomers, temperature, and emulsifier on the stability of the HPAM emulsion and the molecular weight of the HPAM.

为了提高聚丙烯酰胺相对分子质量,以丙烯酰胺与丙烯酸钠为原料,在聚乙二醇水溶液中合成了聚丙烯酰胺水包水乳液,考察了初始单体质量分数、共聚单体与聚乙二醇摩尔比、共聚单体摩尔比、聚合反应温度、乳化剂种类及其浓度对HPAM水包水乳液稳定性及相对分子质量的影响,所得共聚产物相对分子质量可达1.5×10^7。

In this study, Polyurethane/hydrogel composites were fabricated for wound repair applications. The hydrogel was copolymer of thermosensitive N-isopropyl acrylamide and acrylic acid.γ-ray irradiation was employed to copolymerize NIPAAm with AAc and to graft hydrogel onto porous PU simultaneously.

本研究以聚胺基甲酸酯为基材,将感温性异丙基丙烯醯胺(N-isopropyl acrylamide, NIPAAm)和丙烯酸(Acrylic acid, AAc)以γ-ray照射聚合法进行聚合,并同时将水胶接枝在多孔PU上,制备出PU/水胶复材之人工敷料,应用於伤口修复。

The third part of this thesis is reactive simulating calculation In this section, some well-known auxiliaries are selected to compute in density functional theory B3LYP on Gaussian 03, from which the relationship between reaction active energies of transition states and enantiomeric excess of chiral products homoallylic alcohols isobtained based on relative reactive ratio theory. Using this relationship, calculations on the reaction of more than eight auxiliaries with four other aldehydes are carried out in AMI and MNDO, proving that N,N\'-dibenzyl tartamide has higher enantioselectivity than others in this reaction.

第三部分为计算化学部分,运用密度泛函理论B3LYP方法在Gaussian03软件上对已经报道的几种手性配体参与的醛不对称烯丙基化反应过程进行模拟计算,基于相对反应速率理论找出两种构型过渡态间活化能的差异与产物光学收率之间的关系;并以此为基础,用AM1和MNDO方法对上述合成的几种配体控制的反应过程进行量化计算,从而在理论上证实了N-苄基酒石酸二酰胺配体在醛的不对称烯丙基化反应中具有较高的立体选择性。

In a similar way, using N,N\'-dibenzyl tartamide as auxiliary,-(2-methyl)allyl-2-chloro-phenyl-methyl azide, a vital intermediate of Repaglinide, can be prepared via asymmetric allylation of o-chlorobenzaldehyde in

产物经氧化和碘加成内酯化反应得到阿伐他汀中间体(3R,5S)-3-羟基-5-碘甲基戊内酯(10);将N-苄基酒石酸二酰胺用于邻氯苯甲醛的不对称烯丙基化反应以较高光学收率得-甲基烯丙基-2-氯苯基-甲基醇

The polymerization reacts from the inverse emulsion . Selecting white oil as continuous medium , Span60 and TX-10 as the complex emulsifier , AM-01﹑(NH4)2S2O4 and NaHSO3 as new-type complex initiator , the copolymerization of dimethylamino ethyl acrylate methyl chloride/acrylamide was developed . The effects of the concentration of monomer﹑emulsifier and initiator﹑ temperature﹑reaction time and pH on the molecular weight﹑intrinsic viscostity﹑conversion ratio and cation degree of copolymer were studied .

以反相乳液为初始聚合体系,油酸失水山梨醇酯Span60和辛基酚聚氧乙烯醚TX-10构成复配乳化剂,白油为连续介质,AM-01、过硫酸铵和亚硫酸氢钠组成新型复合引发体系,进行丙烯酰胺/(2-甲基丙烯酰氧乙基)三甲基氯化铵的反相准微乳液共聚合,研究了单体浓度、乳化剂、反应温度、反应时间、pH等因素对聚合产品分子量、特性粘数、转化率及阳离子度的影响。

The graft copolymerization of acryalmide and methyl acrylacyl oxyethyl trimethyl ammonium chloride onto chitosan under microwave radiation was studied. The effect of synthesis conditions on graft ratio and graft efficiency, on the strengthening efficacy of the product for wheat straw pulp was studied.

摘 要:研究了用微波辐射的方法进行壳聚糖和丙烯酰胺及甲基丙烯酰氧乙基三甲基氯化铵的接枝共聚反应,讨论了反应条件与产物的接枝效果对麦草浆的增强作用的影响。

It is found that the stereochemistry of the reactions of telluronium allylide,crotonylide and trimethylsilyallylide with α,β-unsaturated esters and amides can be tuned by thechoice of reaction conditions.

利用反应条件的变化首次实现了烯丙基、巴豆基、含硅烯丙基碲叶立德与α,β-不饱和酯、酰胺进行环丙烷反应的立体化学调控,能高立体选择性地、高效率地合成两种不同几何异构体中的一个。

In this article, the factors that affect molecular weight and solubility of polyacrylamide are studied and suitable initiator system is selected. The optimum parameters of copolymerizing process are obtained as follows: the molar proportion of acrylamide and sodium acrylate is 7:3, the monomer concentration is 30%, pH value of solution is 12, the oxidizer (K2S2O8) concentration is 0.1%, the reducing agent (NH2CONH2) concentration is 1%, the chain-transfer agent concentration is 0.4%. The initial reaction temperature is 35℃.

讨论了影响聚丙烯酰胺分子量和溶解性能的因素,选取了合适的氧化-还原引发体系,确定了制备超高分子量速溶型部分水解聚丙烯酰胺的优化聚合工艺参数:起始共聚合反应温度为35℃,保持在密闭条件下的共聚合反应2.5h后,再将聚合反应温度升高到55℃,继续反应2h,反应结束;反应溶液单体总浓度:30%,共聚合反应溶液pH值:12,氧化剂K_2S_2O_8:0.1%,还原剂NH_2CONH_2:1%,共聚合反应中两种单体的投料比:丙烯酰胺:丙烯酸钠=7:3,异丙醇链转移剂:0.4%。

In addition, 65% ee was obtained for 1, 3-dimethylprop-2-enyl acetate. Interestingly, the reactivities of these ligands are all very high.

对于1, 3-二苯基烯丙基醋酸酯的烷基化和胺化反应, ee 值最高分别为93%和98%,此外,在对1, 3-二甲基烯丙基醋酸酯的烷基化反应中 ee 值最高也可达65%。

The results of IR and DSC indicated that the curing reaction of BMI-modified phenolic resin mainly consists of two steps: the allyl groups in the Novolak resin react with maleimide group via"Ene"addition, and addition reactions of the C=C bonds formed thereby are followed.

IR与DSC方法研究表明:BMI改性酚醛树脂的固化反应主要是Novolak树脂上的烯丙基首先与酰亚胺基团的烯加成反应,然后烯加成反应所形成的C=C双键发生进一步加成。

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