期刊文献+

水解聚丙烯酰胺溶液粘弹特性的研究 被引量:22

Study on Viscoelastic Properties of Partially Hydrolyzed Polyacrylamide Solution
下载PDF
导出
摘要 通过锥板测量系统对水解聚丙烯酰胺(HPAM)溶液的粘弹性进行了研究.结果表明,这种锥板测量系统能较灵敏地检测出溶液粘弹性结构的存在,并得到了聚合物溶液的弹性成份和粘性成份的关系.发现随着HPAM溶液浓度的增大,聚合物溶液的弹性成份起初迅速增大,随后增大的趋势变慢而趋于平缓,在经历一最大值后又略有下降.在剪切速率γ珚=0.36s-1下,超高分子量的HPAM(M=1.65×107)溶液(c=1.5g·L-1)具有明显的粘弹特性;随着盐的加入,溶液的粘弹性下降,当盐浓度达到一定值的时候,溶液内部的网络结构遭到破坏,其弹性行为完全消失.对于聚丙烯酰胺(PAAM,M=2.0×105)溶液(c=2.0g·L-1)在剪切速率(γ珚=0.36~1.36s-1)范围内没有观察到粘弹行为,只在γ珚≥1.65s-1时,才能观察到微弱的粘弹现象. In this paper, the viscoelastic properties of partially hydrolyzed polyacrylamide(HPAM) solution were investigated with a cone-and-plate measuring system. Results show that the existence of viscoelastic structure in HPAM solution can be detected quite sensitively by the apparatus. Meanwhile, we also obtained the relationship between the elastic component and the viscous component. It is shown that there exists a maximum value corresponding to the elastic component of solution at the HPAM concentration range of 0. 1 similar to 0. 4 g (.) L At shear rate gamma = 0. 36 s(-1), high molecular weight hydrolyzed polyacrylamide solution has apparent viscoelastic properties. With the addition of salts, viscoelastic properties of HPAM solution decrease. Moreover, the network structures in HPAM solution are destroyed at higher salt concentration, and the elastic behaviors vanish. For PAAM (polyacrylamide) solution, viscoelastic properties weren't observed at the range of 0. 36 similar to 1. 36 s(-1). A weak viscoelasticity was observed only when gamma greater than or equal to 1. 65 s(-1).
出处 《物理化学学报》 SCIE CAS CSCD 北大核心 2004年第11期1385-1388,共4页 Acta Physico-Chimica Sinica
关键词 聚丙烯酰胺溶液 HPAM 弹性成份 粘性成份 粘弹性结构 hydrolyzed polyacrylamide(HPAM) elastic component viscous component viscoelastic properties structure
  • 相关文献

参考文献10

  • 1Doi, M.; Edwards, S. F. The theory of polymer dynamics.Oxford: Clarendon Press, 1986 被引量:2
  • 2Marrucci, G.; Ianniruberto, G. Chem. Eng. Sci., 2001, 56:5539 被引量:2
  • 3Zhang, D. Q.; Cao, Y.; Zhang, H. D.; Yang, Y. L.;Zhang, Y. X. Polymer, 2002, 43:2075 被引量:1
  • 4Lev, B.; Marina, T.; Ralph, H. C. Langmuir, 2000, 16:2609 被引量:1
  • 5Kelarakis, A.; Mingvanish, W.; Daniel, C.; Li, H.;Havredaki, V.; Booth, C.; Hamley, I. W.; Ryan, A.J.Phys. Chem. Chem. Phys., 2000, 2:2755 被引量:1
  • 6Huitric, J.; Meseric, P.; Moan, M.; Jarrin, J. Polymer,1998, 39(20): 4849 被引量:1
  • 7Sato, T.; Watanabe, H.; Osaki, K. Macromolecules, 2000,33:1686 被引量:1
  • 8Effing, J. J.; Mclennan, I. J.; Kwak, J. C. J. Phy. Chem.,1994, 98:2499 被引量:1
  • 9Zhao,F.;Du,Y.K.;Li,X.C.;Tang,J.A.;Yang,P.Chin.Sci. Bulletin,2004,49:335[赵丰,杜玉扣,李兴长,唐季安,杨平.科学通报(Kexue Tongbao),2004,49:335] 被引量:1
  • 10陆铭,孙洪敏,郭燏,杨为民,朱子彬.ZSM-5沸石催化剂的失活历程和活性稳定性[J].石油学报(石油加工),2001,17(4):59-63. 被引量:35

二级参考文献4

共引文献35

同被引文献195

引证文献22

二级引证文献186

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部