超高分子量抗盐型聚合物的合成及性能评价
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O632.63

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Synthesis and performance evaluation of salt-resistant polymer with ultra-high molecular weight
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    摘要:

    采用自由基溶液聚合法合成了丙烯酰胺(AM)/衣康酸(IA)共聚物(IAPAM),用FTIR、1HNMR、元素分析和GPC对其结构进行表征,并对其抗一价、二价阳离子降黏及抗氧化还原物质的能力进行评价。结果表明,IAPAM黏均分子量高达1.716×107。IAPAM抗盐性能评价结果表明,与部分水解聚丙烯酰胺(HPAM)相比,IAPAM有较好的抗一价和二价阳离子降黏的能力,当Na+/Ca2+质量浓度分别为30000、500 mg/L时,IAPAM的黏度分别为196.8、161.56 mPa·s,降黏率分别为22.44%、35.51%。抗氧化还原物质评价实验结果表明,IAPAM具有较好的抗Fe2+和S2-降解的能力,当Fe2+/S2-质量浓度均为10 mg/L时,降黏率分别为23.67%、0.56%,这与共聚单体IA的结构有关。然而,IAPAM对Fe2+的络合稳定作用需要耗费一定时间,未达到络合稳定状态时,Fe2+对聚合物的氧化降解仍然能够进行。

    Abstract:

    The free radical solution polymerization method was used to synthesize acrylamide(AM)/itaconic acid(IA)copolymer IAPAM,its structure was characterized by FTIR,1HNMR,elemental analysis and GPC,and having evaluated the ability of the reducing viscosity of resisting monovalent and divalent cations and resisting redox substances. The experiment determined that the viscosity average molecular weight of IAPAM was as high as 1.716×107. The evaluation results of IAPAM salt resistance performance show that compared with Partially hydrolyzed polyacrylamide(HPAM),IAPAM has better resistance to monovalent and divalent cations to reduce viscosity. When the Na+/Ca2+ concentration is 30000mg/L and 500mg/L,the viscosity of IAPAM is respectively 196.8mPa·s and 161.56 mPa·s,the viscosity reduction rates were 22.44% and 35.51% respectively. The results of anti-oxidation and reduction substance evaluation experiments show that IAPAM has good resistance to degradation of Fe2+ and S2-. When the concentration of Fe2+/S2- is 10mg/L the viscosity reduction rate is 23.67% and 0.56%, respectively. The structure of the monomer IA is related. However, the complex stabilization effect of IAPAM on Fe2+ takes a certain amount of time. When the stable state of complexation is not reached,the oxidative degradation of the polymer by Fe2+ can still proceed.

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吴春元,苏高申,陈思雅,杨欢,于小荣.超高分子量抗盐型聚合物的合成及性能评价[J].精细化工,2021,38(6):

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  • 收稿日期:2020-12-28
  • 最后修改日期:2021-01-25
  • 录用日期:2021-02-01
  • 在线发布日期: 2021-04-07
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