改性丙烯酸-环氧树脂纳米乳液的制备及应用

介绍了水性丙烯酸-环氧树脂纳米乳液的制备及其在油罐防腐工程中的应用。讨论了亲水侧链聚乙二醇相对分子质量大小对涂膜性能的影响以及乳化剂各组分的用量对乳液粒径的影响。     

两性聚丙烯酰胺的合成方法及应用进展

结合国内外研究情况，从技术路线和实施方法两个角度着重阐述了制备两性聚丙烯酰胺的方法，同时简单介绍了其应用情况，并对今后的研究工作提出了一些建议。     

A Semi‐Batch Process for Nitroxide Mediated Radical Polymerization

Summary: A semi‐batch process using nitroxide mediated polymerization, was explored for the design of low molecular weight solvent‐borne coatings, typical of those used in the automotive industry. While living radical polymerization (LRP) offers many advantages in the control of polymer chain microstructure that may confer important physical and chemical property benefits to coatings, adapting LRP to a semi‐batch process poses significant challenges in the design and operation of the process. Using styrene monomer, various two‐component initiating systems (free radical initiator, 4‐hydroxy‐TEMPO) were studied to understand the effects of different initiators on the course of polymerization. In addition, an alkoxyamine was synthesized and used as the initiating source. The initiators Luperox 7M75 and Luperox 231 give higher polymerization rates and reasonable control over polymerization, while benzoyl peroxide (BPO), Vazo 67, and the alkoxyamine are less effective. The number of polymer chains in the final product is always less than the theoretical value, reflecting poor initiation efficiency, probably resulting from undesirable termination reactions that become important due to the nature of the semi‐batch process. Adding camphorsulfonic acid (CSA) or charging initiator concurrently with monomer during semi‐batch feed, can increase the polymerization rate while maintaining the living character of the polymerization. The copolymerization of styrene and butyl acrylate is also shown to exhibit living character.

Schematic representation of the exchange reaction to produce N‐TEMPO capped polymer chains.     

VAc/AA改性的VAE乳液高速接嘴卷烟胶的研制

介绍了VAc/AA改性的VAE乳液高速接嘴卷烟胶的制备方法。研究了各种因素对胶粘剂性能的影响。结果表明 :VAc/AA用量增加 ,VAE乳液的粘接性能增强。选择与VAE乳液相适应的乳化剂和控制适宜的pH值 ,可以增加VAE乳液的稳定性。采用滴加引发剂和混合单体的方法 ,可以避免过速反应产生及大粒径胶粒生成     

Bulk free radical polymerizations of methyl methacrylateunder non-isothermal conditions and with intermediate additionof initiator: Experiments and modeling

Experimental data on the monomer conversion, x_m, and the weight average molecular weight, M_w, have been generated under several isothermal and non-isothermal conditions for the polymerization of methyl methacrylate in a rheometer-reactor assembly. The non-isothermal results, in particular, can be used to provide more stringent tests of kinetic models than isothermal data alone. A simple empirical model has been used to describe this system that accounts for the gel (Trommsdorff) and glass effects. The model involves only x_m and the temperature, and is quite general. The model parameters are tuned using only three sets of isothermal data. Good agreement is found between the experimental results and model predictions for a whole variety of experimental conditions, including non-isothermal operation and with intermediate addition of initiator. Because of its generality, this model is quite suitable for use for on-line optimizing control as well as for describing industrial reactors.     

纳米碳酸钙原位聚合聚氯乙烯树脂的性能及应用

介绍了纳米碳酸钙原位聚合聚氯乙烯的结构和性能,同时对该树脂进行了有关的应用试验,并对其发展前景作了科学展望。     

改性丙-叔共聚乳液在天然石漆生产中的应用

以丙烯酸酯-叔碳酸乙烯酯共聚乳液为基料生产的天然石漆，具有形象逼真、不褪色、耐水耐碱性好、抗紫外线辐射性强等特点。     

聚氨酯-聚丙烯酸酯复合乳液的动态力学性能

采用种子乳液聚合法合成了聚氨酯一聚丙烯酸乙（丁）酯[PU／PE（B）A]复合乳液。并研究了不同组成对复合乳液性质、相客性、阻尼性能及拉伸性能的影响。耐水性及稳定性测试表明，随PE（B）A含量的增加，涂膜的耐水性变好，而乳液的稳定性变差。动态力学性能测试（DMS）表明，合成的PU／PE（B）A复合乳液为半相容体系，其相容性随PE（B）A含量的增加而增强。DMS和拉伸试验表明PU／PEA／P（B）A（质量比50／25／25）复合乳液具有优良的阻尼性能、抗拉强度和断裂伸长率，可用作宽温域阻尼涂料。     

阻燃MC尼龙的研制

通过分析，考察数种阻燃剂对ＭＣ尼龙聚合的影响，总结了ＭＣ尼龙用阻燃剂的特点，筛选出三种适用性较强的阻燃剂，并对其阻燃效果进行了测试和分析。     

Solid‐state polymerization of poly(ethylene terephthalate). I. Experimental study of the reaction kinetics and properties

The solid‐state polymerization (SSP) reaction kinetics of poly(ethylene terephthalate) were investigated in connection with the initial precursor intrinsic viscosity (IV; molecular weight). Evaluations were performed with otherwise equivalent precursors melt‐polymerized to IVs of 0.50, 0.56, and 0.64 dL/g. The changes in the molecular weight and other properties were monitored as functions of the reaction times at solid‐state temperatures of 160–230°C. Precursors with higher initial molecular weights exhibited higher rates of SSP than those with lower initial values, as discussed in connection with the levels of crystallinity and the carboxyl and hydroxyl end‐group composition. Activation energies decreased at temperatures above 200°C, and this indicated a change in the SSP reaction mechanism. At temperatures of 200–230°C, similar activation energies were required for the polymerization of all three precursors. Lower temperature polymerizations, from 160 to 200°C, required higher activation energies for all precursors, with the 0.50‐IV material requirement almost twice as high as that calculated for the higher IV precursors. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 197–212, 2003