甲基丙烯酸锌在NBR／木质素中的应用

研究了α－甲基丙烯酸锌（ＭＡＡ－Ｚｎ）对ＮＢＲ／木质素（１００／１００，质量比）硫化胶性能的影响。结果表明，加入１．５～５．０份ＭＡＡ－Ｚｎ，可提高硫化胺的１００％的定伸应力，硬度和抗压缩永久变形能力，但对其他力学性能影响甚微，经分析可知，ＭＡＡ－Ｚｎ还可以降低硫化反应活化能，提高硫化胶的交联密度和耐热老化性能。     

不变黄HDI-PU/P(MMA-HEMA)互穿网络胶粘剂形态与性能的研究翁祥

制备了HDI(1,6-己二异氰酸酯)型聚酯聚氨酯/聚(甲基丙烯酸甲酯-甲基丙烯酸-β羟乙酯)(HDI-PU/P(MMA-HEMA))互穿网络胶粘剂,研究了接枝剂甲基丙烯酸-β羟乙酯(HEMA)用量对其形态、性能与分子结构的影响。结果表明,接枝剂HEMA可使分散相接枝到连续相中形成复合网络,从而改善其界面的相容性,提高其胶液粘度和初粘力,并可广泛作为制鞋工业用胶。     

国内外AE／AES生产现状及市场分析

介绍国内外脂肪醇聚氧乙烯醚(AE)和脂肪醇聚氧乙烯醚硫酸盐(AES)的生产现状及供需情况.2003年全球AE的总产能为391.7万t/a,总产量为155.8万t,总消费量为148.3万t;AES的总产能为377.5万t/a,产量约为300万t,消费量约为90万t.2004年我国AE的产能已超过50万t/a,但产量只有15万t,消费量为30.5万t;AES的总产能为37.95万t/a,产量为14万t,市场需求约10万t.最后补充介绍乙氧基化的技术进展.     

Effects of preparation conditions on the surface modification and performance of polyethersulfone ultrafiltration membranes

The impact that some membrane preparation steps had on ultrafiltration (UF) membrane characteristics and performance was studied. Polyethersulfone (PES) was employed as base polymer, while N‐methyl pyrrolidone (NMP) was used as a solvent, and polyvinylpyrrolidone (PVP) was used as a nonsolvent pore‐forming additive. The manufacturing variables studied were solvent evaporation time and membrane surface modification, using a fluorine‐based copolymer referred to as surface‐modifying macromolecule (SMM). The flat sheet membranes, prepared via phase inversion, were characterized using solute transport data, X‐ray photoelectron spectroscopy (XPS), and contact angle measurements. Membrane performance was evaluated via filtration test protocol that included a 6‐day filtration of concentrated river water. The flux reduction with time was modeled using single and dual mechanisms of fouling. The pore blockage/cake filtration model described better the behavior of the permeation rate along the experiments. Increasing the solvent evaporation time decreased the size of the pores and the permeation rate. However, it did not significantly affect the removal of the organic compounds naturally present in the river water used as feed. XPS and contact angle measurements proved that the short evaporation periods did not allow enough SMM migration to the surface to provoke a significant effect on the membrane performance. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci, 2006     

柴油替代燃料二甲醚的应用开发和发展概况

详细介绍了二甲醚作为柴油替代燃料的开发和应用情况。以天然气为原料制二甲醚，天然气价格对产品成本影响非常大，目前二甲醚作为柴油替代燃料还不具备和柴油竞争的优势，相比之下合成气一步法工艺技术更具有竞争优势。概述了我国二甲醚发展现状，并对我国二甲醚发展提出了建议。     

环氧稀释剂十二烷基缩水甘油醚的合成

对稀释剂十二烷基缩水甘油醚的合成及影响产品质量的因素进行了研究,并以十二、十四混醇为原料进行了对比试验。     

ESI-MS法对重烷基苯烃基结构的研究

采用多种分析手段,其中以电喷雾质谱为主的方法研究了重烷基苯的烃基结构。首先通过柱色谱法对重烷基苯进行分离,将其分成了六个族组分。通过各族组分的红外、紫外鉴定,确定它们各自的归属,用电喷雾质谱测定Ⅱ～Ⅴ族组分磺酸盐的相对分子量分布,结合红外、紫外测定的结果及每族物质的不饱和度和通式,推算出了烷基芳烃部分的相对分子质量和烷基的碳数分布。重烷基苯中几个主要成分的碳数分布为:其中二烷基苯的碳数分布在10～25之间,单烷基苯的碳数分布在10～25之间,烷基萘的碳数分布在5～20之间,烷基二联苯的碳数分布在4～19之间。     

聚甲基丙烯酸缩水甘油酯为主链的咪唑型螯合树脂的合成、表征及吸附性能研究

用分散聚合法合成了聚甲基丙烯酸缩水甘油酯(PGMA),然后引入咪唑功能基合成了螯合树脂(PGMA-Imi),用傅立叶变换红外光谱(FTIR)与扫描电镜(SEM)研究了其结构与粒子表面形态,元素分析测定功能基含量,并对Cu2+等离子进行了吸附研究。结果表明所得PGMA微球为微米级、单分散性很好,所得螯合树脂(PGMA-Imi)对Cu2+的吸附效果最好。     

二甲醚燃烧用掺杂钡、镍六铝酸盐催化剂的研究

二甲醚是易液化，便于运输，清洁化的新能源。当作为燃料使用时，采用催化燃烧的方法能使得燃烧的起燃温度降低和提高燃烧转化率，克服了普通燃烧的缺点，实现了清洁燃烧。对二甲醚催化燃烧用的催化剂BaNiAl11O19-δ进行了制备与研究。采用溶胶-凝胶法制备六铝酸盐催化剂BaNiAl11O19-δ,考察其对新能源二甲醚催化燃烧反应的活性，并用TG—DTA对催化剂的性质进行考察。结果表明，加入经800℃焙烧4h后又在1200℃焙烧了2h的催化剂，比未加催化剂的燃烧体系T10降低了50℃。用溶胶一凝胶法制备的六铝酸盐催化剂BaNiAl11O19-δ对二甲醚催化燃烧反应具有较高的催化活性。     

Enzymatic production of alkyl esters through alcoholysis: A critical evaluation of lipases and alcohols

This paper focuses on a detailed evaluation of commercially available immobilized lipases and simple monohydric alcohols for the production of alkyl esters from sunflower oil by enzymatic alcoholysis. Six lipases were tested with seven alcohols, including straight and branched-chain primary and secondary alcohols. The reactions were conducted in a batch stirred reaction vessel using stoichiometric amounts of substrates under solvent-free conditions. Dramatic differences in alcoholysis performance were observed among the different lipases. For most of the alcohols, Novozym 435 produced the highest yield of FA alkyl esters, with yields well over 90% for methanol, absolute ethanol, and 1-propanol. Overall, 96% ethanol was the preferred alcohol for all lipases except Novozym 435, and ethanolysis reactions reached the maximal conversion efficiency. Increasing the water content in the system resulted in an increased degree of conversion for all lipases except Novozym 435. The secondary alcohol 2-propanol significantly reduced the alcoholysis reaction with all lipases; however, the branch-chain isobutanol was more advantageous than linear 1-butanol for Novozym 435, Lipozyme RMIM, and Lipase PS-C. Many commercial immobilized lipases are highly efficient and promising for the production of alkyl esters, offering high reaction yields and a simple operation process.