首页 | 本学科首页   官方微博 | 高级检索  
     检索      

马铃薯淀粉高吸水性树脂的合成及性能研究
引用本文:张文英,韩燕,党斌.马铃薯淀粉高吸水性树脂的合成及性能研究[J].青海大学学报,2013(5):57-64.
作者姓名:张文英  韩燕  党斌
作者单位:青海大学农林科学院,青海西宁810016
基金项目:青海大学农林科学院创新基金
摘    要:为优化马铃薯淀粉高吸水性树脂的合成工艺,采用水溶液聚合法进行接枝共聚制备高吸水性树脂,并对其性能进行研究.结果表明:当马铃薯淀粉与单体(g/mL)比例为1:7,丙烯酸与丙烯酰胺摩尔比为0.5:1,丙烯酸中和度为70%,反应温度60℃,引发剂、交联剂用量分别为单体的0.25 wt%,0.6 wt%,交联时间为1.5h.此条件下合成的高吸水性树脂吸蒸馏水倍率达到786 g/g,吸0.9% NaCl倍率达到76.1g/g,且吸水速率较快.对人工血、人工尿及一价阳离子溶液有较好的吸收率;热稳定性较好,保水能力强,在室温条件下保水能力在7d左右;在30、40、50、60℃条件下保水能力均优于科翰98保水剂,但耐酸性较差,在中性偏碱的条件下具有很好的吸水倍率.

关 键 词:马铃薯淀粉  高吸水性树脂  合成  性能

Synthesis and property of superabsorbent polymer with potato starch
ZHANG Wenying,HAN Yah,DANG Bin.Synthesis and property of superabsorbent polymer with potato starch[J].Journal of Qinghai University(Natural Science),2013(5):57-64.
Authors:ZHANG Wenying  HAN Yah  DANG Bin
Institution:( Academy of Agriculture and Forestry, Qinghai University, Xining 810016, China)
Abstract:In order to optimize the synthesis conditions of super absorbent polymer(SAP) with pota- to starch, it was prepared by aqueous solution polymerization method, and its properties were stud- ied. The results are as follows, when mass ratios of starch to monomer is 1 : 7, mole ratio AA to AM is 0. 5: 1, degree of neutralization is 70%, reaction temperature is 60 ℃, the amounts of initiator, crosslinking agent are 0. 25% and 0. 6% ,cross - linking time is 1.5 h, the absorption of distil water by super absorbent polymer is 786 g/g,and absorption power in 0. 9% NaCl is 76. 1 g/g at a faster rate of water absorption. The absorption rate of the artificial blood, the artificial urine and price posi- tive ion solution were better. The SAP had good thermal stability and strong water retention ability, the water retaining capacity were 7 days. It displayed better water retaining capacity than Kehan 98 SAP at 30 ℃ ,40 ℃ ,50 ℃ and 60℃. The acid resistance was bad,but had very good water absorb- ency under the neutral weak alkali condition.
Keywords:potato starch  super absorbent polymer  synthesis  property
本文献已被 维普 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号