Preparation and properties of novel polyurethane insulating coatings based on glycerin‐terminated urethane prepolymers and blocked isocyanate

Novel polyurethane insulating coatings were prepared from the reaction of glycerin‐terminated polyurethane prepolymers (GPUPs) and a blocked isocyanate curing agent (BIC). The GPUPs were prepared from the reaction of one equivalent of polycaprolactone polyol (CAPA 210) with an excess amount of 4,4′‐methylene bis(phenyl isocyanate) (MDI) and subsequent reaction of the NCO‐terminated polyurethane with glycerin. The BIC was prepared from the reaction of trimethylol propane (TMP), toluene diisocyanate (TDI) and N‐methylaniline (NMA). The polyols and curing agent were characterized by conventional methods while the curing condition was optimized via gel content measurements. The curing kinetics of the polyurethane coating were investigated and the kinetic parameters derived. The crosslink densities of the samples were determined via the equilibrium swelling method, using the Flory–Rehner equation. The relationships between the crosslink density and the electrical, physical, mechanical and dynamic mechanical properties of the coatings were also studied. Copyright © 2005 Society of Chemical Industry     

Effect of ionic content,solid content,degree of neutralization,and chain extension on aqueous polyurethane dispersions prepared by prepolymer method

There are many variables in the preparation of aqueous polyurethane (PU) dispersions. Carboxylic acid content, solid content, degree of pre/postneutralization of the carboxylic acids, and chain extension all impact dispersion particle size, viscosity, pH, molecular weights, and glass transition temperature. This study evaluated the impact of these variables on a given PU dispersion formulation prepared from isophorone diisocyanate, an aliphatic polyester polyol, dimethylol propionic acid, and hexamethylene diamine with triethyl amine as the neutralizing base and N‐methyl pyrrolidone as the cosolvent. Changes in carboxylic acid content, degree of preneutralization, and chain extension were found to have the expected impacts on dispersions properties. Increased ionic content in the dispersion step led to lower particle size and higher viscosity, increased chain extension with its concurrent increase in molecular improved subsequent film properties. Surprising results were obtained by varying the amount of postneutralization and from increased solids content at the time of dispersion. Unexpectedly, both of these variations led to much higher dispersion viscosities and particle size in solution. To have these changes take place, it is theorized that there is a major change in solution morphology caused by these modifications. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 2514–2520, 2005     

泡沫酸化工艺对川中低压裂缝性油藏适应性的认识

针对川中油田经过多年的消耗式开采,各主产油田压力很低,增产改造的难度增大的发展现状,提出应用泡沫酸化工艺技术在川中低压油层增产改造的技术方案,其中分析了泡沫酸的物理特性、其在地层优良的渗流特性(滤失小、酸岩反应速度慢、返排迅速等优点),并进行了泡沫酸液体系的室内配方研究,提出了工艺设施的矿场配套研究内容.得出了泡沫酸化工艺对川中低压裂缝性油藏改造具有很强的适应性,具有推广应用的价值.     

PMMA／PBA乳胶IPN阻尼材料的研究

用乳液聚合方法合成了一系列的互穿聚合物网络，其中包括：ＰＭＭＡ／ＰＢＡ和Ｐ（ＭＭＡ－ｃｏ－ＰＭＡ）／ＰＢＡ乳胶互穿聚合物网络（ＬＩＰＮ），ＰＭＭＡ／ＰＢＡ乳胶双向互穿聚合物网络（ＬＢＩＰＮ）以及ＰＭＭＡ／ＰＢＡ界面交联互穿聚合物网络（ＩＣＬＩＰＮ）。动态力学谱和拉伸试验结果表明：（１）ＰＭＭＡ／ＰＢＡ互穿聚合物网络的两组分相容性和阻尼性能可通过ＭＭＡ和ＰＭＡ共聚来改善；（２）双向互穿技术是一种行之     

红外研究丁羟二异氰酸酯的固化反应动力学

用红外分光光度计研究了端羟基聚丁二烯(HTPBD)与二异氰酸酯的反应动力学,结果表明,NCO与OH的反应为二级动力学反应,由于位阻效应和共轭效应,MDI比TDI的反应活性大得多,前者的反应速率常数大约是后者的10～20倍。反应速率常数及活化能随NCO的过量而有所变化。在NCO过量体系中。TDI-HTPBD体系中有次级反应发生,由于氢键的作用,次级反应为对于氨基甲酸酯基为二级、NCO为一级的三级反应动力学.由于位阻效应,MDI体系很难发生次级反应。     

聚四氢呋喃及其下游产品的开发应用

本文论述了聚四氢呋喃技术进展、氨纶弹性纤维发展现状和国内外聚四氢呋喃产能和需求。     

聚氨酯IPN的研究——制备方法与性能的关系

介绍了聚氨酯 IPN合成技术的主要特征 ,PU预聚体分子量大小、NCO/ OH的比值 ,互穿网络的方式及反应温度、速率对性能的影响     

聚氨酯泡沫夹克管生产材料的代用

介绍一种用于生产聚氨酯泡沫夹克管保温层的新材料聚酯聚醚，报道选用这种材料生产泡沫夹克管的工艺及工要工艺参数和产品达到的技术指标及现场应用情况。     

制革用水乳型聚氨酯涂饰剂行业标准的制定

本文概述了制定该标准的背景，对标准的主要内容加以科学的阐述。     

含聚二甲基硅氧烷的聚醚聚氨酯膜透气性及表面性质研究

以聚二甲基硅氧烷（ＰＤＭＳ）／聚四氢呋喃（ＰＴＭＯ）为软段，４，４＇－二环己基甲烷二异氰酸酯（ＨＭＤＩ）为硬段（丁二醇ＢＤ为扩链剂）制成的多相嵌段共聚物作为基质材料，进行了气体（Ｏ２和Ｎ２）透过性试验，同时对膜材料进行了ＥＳＣＡ表面分析。结果表明，共聚物膜的透气性能取决于材料中连续相组分，随着软段中ＰＤＭＳ含量的改变而变化。当ＰＤＭＳ含量较高时，共聚物膜显示出ＰＤＭＳ均聚物的特性，具有较高的气体秀