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作 者:赵仁保[1,2]
机构地区:[1]中国石油大学北京石油工程教育部重点实验室 [2]提高采收率研究中心,北京102249
出 处:《高等学校化学学报》2009年第3期596-600,共5页Chemical Journal of Chinese Universities
基 金:国家“九七三”计划(批准号:2006CB705800);国家科技支撑计划(批准号:2007BAB17B05和2006BAB03B06)资助
摘 要:研究了不同CO2分压下低浓度丙烯酰胺(AM)在硅酸钠溶液中的聚合反应行为,用环境扫描电子显微镜、流变仪及激光粒度仪等研究了产物的微观结构及其流变特性.结果表明,随着CO2浓度的增加,产物的储能模量增加,即黏弹性增大;反应后生成的硅酸凝胶镶嵌在聚丙烯酰胺高分子凝胶网格中形成了复杂的网状结构.在超声波作用下,硅酸凝胶颗粒从体系中脱离,检测到的颗粒粒径范围在280~900nm之间,且随着超声时间的增加,颗粒的平均粒径减小.结果表明,CO2的存在使得AM及交联剂的分子扩散速度增加,提高了AM分子之间及其与交联剂分子的接触几率,从而提高了产物的分子量.The polymerization behavior of acrylamide at its low concentration in sodium silicate solution under different pressure of carbon dioxide was studied. The microstructure and rheologieal properties of the synthetic products were characterized by environmental scanning electron microscope ( ESEM), rheometer and laser par- ticle sizer. A mixture is produced in experiments and will have larger storage modulus or viscoelasticity at a higher CO2 concentration. It has a complex network structure formed by silicie acid gel embedded into polyac- rylamide gel. After detaching from the mixture when exposed to ultrasonic wave, the silicate granules have a particle size distribution range of 280--900 nm, and their average size becomes smaller with the increase of exposure time. The mechanisms is that carbon dioxide helps increase both the diffusion velocity of AM mole- cule and also contact chance among the AM and initiator and cross linking agent, which could enhance the molecule weight of the products.
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