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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 synthesized PCU was then characterized by infrared spectroscopy, differential scanning calorimetry, thermogravimetric analysis, small-angle X-ray scattering, and tensile strength measurement. The IR showed that the polymer synthesized by the above two methods both have the polycarbonate-urethane structure and the tensile measurement showed good mechanical performance of the polymer. The DSC and TGA data showed that there is an obvious soft-hard glass transition area, which indicated the existence of the micro-phase separation structure. The extent of the phase separation was affected by the ratio of starting materials, the molecular weight of PCD, and the polymerization method. The decomposition upon heating was observed in two steps. SAXS result showed that the radius (r_2), the distance between domains (d_2), and gyral radius (R_2) of hard segment micro-domain were fairly affected by the starting materials ratio and soft segment content.

IR结果表明两种方法合成的聚合产物均具有聚碳酸酯聚氨酯的结构;拉伸实验表明聚合产物具有良好的力学性能;DSC、TG结果表明,聚合物呈现出较为明显的软硬段玻璃化转变区,表明存在微相分离的结构,相分离的程度受原料配比、软段分子量、聚合方法的影响,其热分解分为明显的两个阶段; SAXS结果表明,聚合物原料配比、软段含量的变化对硬段微区回旋半径R_2,微区间距d_2,微区半径r_2影响不大其值分别为9.5(A|°、29、7.4,但对软段的微区半径及间距影响较大,随着软段含量的增大,软段微区的半径r1和间距d1都增大。

The stability of isophorone disocyanate and the affecting factors of in-situ miniemulsion polymerization have been studied to carry out the simutaneous or two-step procesure of polyaddition and radical polymerization.

本文主要研究了水敏性单体IPDI的稳定性和原位细乳液聚合规律,探索在细乳液中分步或同步实现缩聚反应与自由基聚合的新方法,提出了水敏性单体的细乳液聚合实施方法。

The photopolymerization led to stable latices and they were obtained with neither coagulation during synthesis nor destabilization over time. It was found that the obtained MMA homopolymers exhibited relatively narrow molecular weight distributions(PDI=1.27—1.36), which was characterized by GPC. The plots of number-average molecular weight vs. conversion and ln([M0]/) vs. time were linear respectively, indicating that the reaction was a controlled/living free radical polymerization.

结果表明,该细乳液体系非常稳定,在整个聚合过程中即没有絮凝物产生,也没有沉淀析出,获得了良好的ln([M0]/)与时间、数均分子量与转化率之间的线性动力学关系,并且在整个聚合反应过程中MMA均聚物的分子量分布比较窄,其多分散性指数较低(PDI=1.27~1.36),具有明显的活性聚合特征。

The result indicate that P has much greater initiation ability in comparison with monomeric MABP, but P does not.

聚合的引发体系的优点在于它不仅能够引发聚合而且能够参与聚合,进人聚合物链中。

The aim of this study was to develop a novel amphiphilic functional block poly(ε-caprolactone) bearing ketone groups MPEG-b-P(OPD-co-CL. 2-oxepane-1, 5-dione was copolymerized with ε-caprolatone in which methoxy poly (MPEG, Mn=5 000) and stannous octoate were used as initiator and catalyst, respectively. The syntheses were conducted by bulk and solution polymerization. 1H NMR results showed that peak position and splitting of the polymers synthesized through solution polymerization were consistent with theoretical data, demonstrating the products were designed block copolymers. While in the bulk polymerization, polymer peak position was changed due to their high reaction temperature, suggesting their structural variation.

将带有羰基官能团的4-羰基己内酯和ε-己内酯分别在甲氧基聚乙二醇(MPEG,Mn=5 000)为引发剂,异辛酸亚锡为催化剂溶液和本体体系中开环聚合,合成了两亲性侧基带有羰基官能团的聚己内酯嵌段共聚物MPEG-b-P(OPD-co-CL.1H NMR结果表明采用溶液聚合法合成的聚合物各峰的峰位置和分裂情况与理论一致,证明了产物是实验所设计的嵌段共聚物,而采用本体聚合法合成的聚合物由于温度的影响,聚合物各峰的峰位置发生了变化,说明其结构发生了变化;差示扫描量热法分析结果表明随着OPD单体含量的增加,聚合物的熔点,玻璃化转变温度和熔融焓增加;热失重测试结果表明OPD单体的引入增加了聚合物的热敏感性。

In this article, star-high vinyl content polybutadiene was prepared using a multi-functional organolithium anionic initiator by " one-step " process. On the basis of 250ml glassware experiment ,we improved the experiment in 2L metal kettle. The polymerization condition was got as follows: polymerization temperature : 50-60 ℃, monomer content : 8-llg/100ml, polymerization time : 3~4 hours.Chracterizations were carried out by 'H-NMR, IR and GPC.

本文首次采用多官能团有机锂引发剂一步法合成出了星型高乙烯基聚丁二烯,在250ml玻璃瓶的基础上,进行2L金属斧的扩大实验,确定了以下聚合工艺参数:聚合反应温度:50~60℃,单体浓度:8~11g/100ml,聚合反应时间:3~4小时。

The electric conductivity of solid polyiodides increases largely as the aggrandizement of polyiodide anions"polymerization degree. The solid polyiodides have excellent sterilizing effects and the effect of tetra-n-butyl ammonium undecaiodide is the best of them, and the sterilizing effects increase as the aggrandizement of polyiodide anions" polymerization degree. The sterilizing effects of resinic polyiodides increase as the aggrandizement of polyiodide anions polymerization degree, the heptaiodide resinic polyiodide has better sterilizing effects than the triiodide and pentaiodide.

固体高聚碘系列化合物的电导率随着高聚碘阴离子聚合度的增加而增加,并且增幅较大;固体高聚碘对常见细菌均具有很好的杀灭作用,并且随着高聚碘阴离子聚合度的增加,杀菌能力也随着增强,其中正四丁基十一碘化铵杀菌剂的效果最佳;树脂高聚碘随着高聚碘阴离子聚合度的增加,杀菌能力增强,碘七树脂高聚碘的杀菌效果要明显好于碘三树脂和碘五树脂高聚碘。

For VC suspended emulsion polymerization initiated by potassium persulphate, the initial polymerization rate is proportional to 133 and proportional to RpJ0 72, where

以 KPS为引发剂进行的 VC悬浮态乳液聚合,基本上是在隔离的小水滴内进行的,类似于乳液聚合机理,但齐聚物自由基的相转移可以引发少量的单体相聚人采用优化的聚合工艺条件,得到转化率大于70%、颗粒仍由基本不熔结的初级粒子组成、吸油率为 19。

By using the hydrochloric acid pickling wastewater and scrap iron asraw materials ,the polysilicic acid - polyferric chloride flocculant isprepared under different conditions.

以盐酸酸洗废液和废铁屑为原料,制备了聚硅酸聚合氯化铁复合型絮凝剂,研究了聚铁中铁浓度、聚合硅酸浓度、聚合硅酸pH值、n∶n及复合熟化时间等因素对絮凝性能的影响。

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