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polymerization相关的网络例句

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与 polymerization 相关的网络例句 [注:此内容来源于网络,仅供参考]

The new type of polymerization was named as in situ ATRP. The in situ ATRP of MMA with TD/FeCl3/PPh3 in bulk and in anisole was well-controlled polymerization.

由引发体系组分间的反应原位产生氯化物引发剂 Et2NCS2Cl和催化剂FeCl2后按ATRP方式反应,称为in situ ATRP。

The graft copolymer has an optimum effect of pour point depressing for the Daqing crude oil when it was synthesized under the conditions of that the mole ratio of EVA and octadecyl maleimide was 1:20, mass fraction peroxidation benzoin formyl was 2.5%, polymerization time was 6h, and the polymerization temperature was 90℃.

以目标物的降凝幅度为评价指标,优选出适合的合成条件为:EVA与十八烷基马来酰亚胺的摩尔比为1:20,引发剂过氧化二苯甲酰的量为2.5%,聚合时间6h,聚合温度为90℃。

The proper in-situ polymerization systems of acidic and basic compounds using amino acid derivatives and cinchona alkaloids as template molecules respectively were adopted for preparation of molecularly imprinted monolithic columns by systematically investigating the effect of polymerization conditions on pore structure and selectivity of resulting polymers. The enantiomers of amino acid derivatives and the diastereomers of cinchona alkaloids were successfully resolved on these columns.

本文分别以氨基酸衍生物和辛可纳生物碱为模板分子,系统研究了制备条件对聚合物孔结构和选择性的影响,建立了合适的酸性化合物和碱性化合物的原位印迹体系。

In order to explore the mechanism of polymerization between lignin from effluent of pulping process and lignin precursors, the method and mechanism of co-polymerization of coniferin with model compound of β-O-4 type lignin were investigated.

为了探讨造纸废水中残余木质素与木质素前驱物之间的聚合反应机理,研究了β-O-4型木质素模型化合物与木质素前驱物松柏醇-β-D-葡萄糖苷-[α-13C]的聚合反应方法及其反应机理。

Poly/melamine cyanurate composite latex particles are prepared via soapless emulsion polymerization. XPS data and TGA analysis reveal that MC particles are encapsulated by PMMA during polymerization, resulting in the formation of a core-shell structure of PMMA/MC composite latex particles. MC can affect the thermal degradation and promote the charring of PMMA. The application of PMMA/MC in nylon 6 (PA6) indicate that the composite latex particles can improve the mechanical pro...

采用原位乳液聚合法制备了聚甲基丙烯酸甲酯/三聚氰胺氰尿酸盐复合胶粒,对其进行X光电子能谱及热重分析结果显示,在MC阻燃剂颗粒表面覆盖了一层PMMA胶膜,形成了具有核-壳结构的PMMA/MC复合胶粒;MC能影响PMMA的热降解过程并促进其成炭;在尼龙6(PA6)中的应用结果表明,PMMA/MC复合胶粒能改善PA6的力学性能和阻燃性能。

New contributions of this work are as follows:(1). Preparation of Spherical MgCl_2-Supported Late-Transition Metal Catalysts for Ethylene Polymerization Facile and effective immobilization of late-transition metal catalysts. 2,3-bis-(2,6-diisopropylphenyl) butane diimine nickel dibromide (1) and 2,6-bis-[1-(2,4,6-trimethylphenylimino)ethyl]pyridine iron dichloride (2), for ethylene polymerization has been achieved, using spherical MgCl_2 supports obtained by thermal dealcoholization of MgCl_2·2.56C_2H_5OH, and the effects of dealcoholization temperature on supported late-transition metal catalysts and the properties of resultant polymers were studied, the results indicated that: 1.Supports with appropriate mechanical strength, high surface area and high porosity could be prepared by thermal dealcoholization of spherical MgCl_2·2.56C_2H_5OH supports; 2.BET, XRD, IR, SEM, GPC and DSC analyses indicate that the activities of the supported late-transition metal catalysts and the properties of resultant polymers are strongly dependent on the dealcoholization temperature.

本工作的新贡献如下:(1)、球形氯化镁负载后过渡金属催化荆催化乙烯聚合本文将配合物2,3-双(2,6-二异丙基苯亚胺)丁烷二溴化镍(1)和配合物2,6-二[1-(2,4,6-三甲基苯亚胺)乙基]吡啶二氯化铁(2)分别直接负载于经不同热脱醇温度处理的球形氯化镁载体上,研究了氯化镁载体的脱醇温度对负载化后过渡金属催化剂及其聚合物的影响,研究表明: 1、通过对球形MgCl_2·2.56C_2H_5OH载体进行热脱醇处理,可以获得合适机械强度、较高比表面积和较高孔隙度的球形氯化镁载体; 2、BET,XRD,IR,SEM,GPC和DSC研究表明,脱醇温度极大地影响负载后过渡金属催化剂的活性和聚合物的性能。

The results show that, the static interfacial polymerization was conducted in organic phase. The optimized conditions for NF membrane preparation were obtained: the concentration of PDMAEMA was 2%, the concentration of p-xylylene dichloride was 1 ~ 1.5%, NaHCO_3 can be used to maintain alkalescence, The polymerization can be carried out at room temperature and the reaction time was 5 hour.

研究结果如下:此界面聚合反应在有机相中进行;较优的制备条件为:PDMAEMA浓度为2%,对二氯苄浓度为1~1.5%,应加入少量的NaHCO_3来维持溶液的微碱性,室温下反应即可进行,反应时间为5小时。

The effect on polymerization reaction and polymer with the catalyst system is systematacially studied in this paper, and the polymerization kinetics of butadiene is determined by dilatometer method.

本文系统的研究了该催化剂体系对聚合反应及其产物的影响,以膨胀计法测定了丁二烯聚合反应动力学。

Studies are carried out on the feasibility of two kinds of sulfates as the dispersion medium of CPAM dispersion polymerization, as well as the impact of different kinds of dispersants on CPAM dispersion polymerization.

考察了CPAM分散聚合中,两种不同硫酸盐作为分散介质的可行性,并详细讨论了不同类型的分散剂对盐水介质中CPAM分散聚合的影响。

Discussed the ratio of alcohol/water for dispersion medium, the polymerization temperature and stirs speed factor and so on to the polymerization system stability, microspheres particle size and its distribution influence.

考察了分散介质的醇水比、聚合温度及搅拌速率等因素对聚合体系的稳定性、微球粒径及其分布的影响。

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