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反相悬浮聚合法合成可生物降解海藻酸钠高吸水性树脂 被引量:8

Synthesis of Biodegradable Sodium Alginate Super Absorbent by Inverse Suspension Copolymerization
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摘要 以丙烯酸(AA)和海藻酸钠(SA)为原料,用反相悬浮聚合法合成了聚丙烯酸钠/海藻酸钠高吸水性树脂。研究了海藻酸钠、引发剂(KPS)和交联剂(NMBA)用量、丙烯酸中和度、聚合反应温度等因素对树脂吸水率的影响以及树脂的生物降解性能。结果表明,当w(SA)=1.5%、w(KPS)=0.15%、w(NMBA)=0.1%、丙烯酸中和度为65%、聚合反应温度为75℃时,树脂对蒸馏水的吸水率为845 g/g,对生理盐水的吸水率为88 g/g,且能被土壤和微生物降解,w(SA)=10%的树脂在60 d内能够被芽苞杆菌降解52%,在土壤中能被降解36%,且降解速度随海藻酸钠质量分数的增加而加快。IR测定表明,树脂为丙烯酸盐与海藻酸钠的接枝共聚物。SEM测定表明,PAA/SA高吸水性树脂呈花瓣结构。 Poly ( sodium acrylate) / ( sodium alginate) super absorbent resin was synthesized by inverse suspension copolymerization using partially neutralized acrylic acid ( AA ) and sodium alginate ( SA ). The influences of sodium alginate, crosslinking agent ( NMBA), initiator ( KPS), neutralization degree of AA and copolymerization temperature on absorbency and biodegradability of the resin were studied. The resuhs showed that when w ( SA ) = 1.5%, w ( KPS ) = 0. 15%, w ( NMBA ) = 0. 1%, neutralization degree of AA is 65%, and reaction temperature is 75 ℃, the absorbency of the resin is 845 g/g for distilled water or 88 g/g for normal saline, and can be degraded by soil and microbes. The degradation rate of the resin [w(SA) = 10% 3 is 52% by spore bacilus or 36% in soil within 60 days,and the degradation rate speeds up with the increase of W(SA). IR indicated that the resin is graft copolymer of acrylic acid with sodium alginate. SEM showed that the structure of the resin is like flower petals.
出处 《精细化工》 EI CAS CSCD 北大核心 2006年第3期218-222,共5页 Fine Chemicals
基金 国家自然科学基金(20376087)资助项目~~
关键词 高吸水性树脂 聚丙烯酸钠 海藻酸钠 生物降解 super absorbent poly( sodium acrylate) sodium alginate biodegradability
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  • 1路建美,朱秀林,顾梅.微波法合成聚丙烯酸钠高吸水性树脂[J].高分子材料科学与工程,1996,12(4):55-58. 被引量:39
  • 2原敏夫 板东彻.[P].特开平11 343339..
  • 3邹新禧.超强吸水剂(第2版)[M].北京:化学工业出版社,2001.473-638.
  • 4原敏夫 板东彻.[P].特开平 11 343339..
  • 5[1]G.F. Fanta, R. C. Burr. Graft Copolymers of Starch. I Copolymerization of Gelatinized Wheat Starch with Acrylonitrile: Fractionation of Copolymer and Effect of Solvent on Copolymer Composition [ J ]. J. Appl.Polmer Sci., 1996, 10: 929
  • 6[2]G.F. Fanta, R. C. Burr. Graft Copolymers of Starch. Ⅱ Copolymerization of Gelatinized Wheat Starch with Acrylonitrile: Influence of Reaction Conditions on Copolymer Composition [ J ]. J. Polymer Sci., 1966,B4:765
  • 7[3]G.F.Fanta,R.C.Burr. Graft Copolymers of Starch. Ⅲ Copolymerization of Gelatinized Wheat Starch with Acrylonitrile: Influence of Chain Modifiers on Copolymer Composition [ J ]. J. Appl. Polymer Sci, 1967,11:457
  • 8温品谦二.ス-パ-アづソ-ベント[J].有机合成化学协会志,1980,38(6):546.
  • 9[6]高吸水性树脂展望[N].化学工业时报,1979年11月25日,No.1698
  • 10[7]SOON HONG YUK, et al. A Novel semi-interpenetrating networks system as an absorbent material[J]. Eur. Polym. J., 1996, 32( 1 ): 101-104.

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