微波等离子体引发共聚法制备丙烯酰胺磺化共聚物

F. Ghomashi, S. Kooshki, B. Shokri
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引用次数: 0

摘要

在水溶液中通过等离子体引发共聚得到了丙烯酰胺(AM)与2-丙烯酰胺-2-甲基丙烷磺酸(AMPS)的共聚物。研究了放电时间和放电功率等等离子体参数对合成共聚物特性粘度[η]的影响。用质子核磁共振波谱(1H-NMR)和傅里叶变换红外光谱(FTIR)对共聚物进行了表征。用热重分析(TGA)研究了共聚物的热行为。[η]随放电功率变化的结果表明,放电功率为150W时,[η]的最佳值为27.12 dl/g,之后[η]开始下降。对不同放电时间下的[η]进行了测定,结果表明,放电时间30s时,[η]的最佳值为26.03 dl/g。TG数据显示了两个失重阶段,第一个阶段发生在270°C到330°C之间,失重约40%,第二个阶段发生在350°C到460°C之间,失重约25%。结果表明,所制共聚物适用于提高采收率工艺。
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Synthesis of sulfonated copolymers of acrylamide by plasma-initiated copolymerization using microwave plasma
The copolymers of acrylamide (AM) and 2-acrylamido-2-methylpropane sulfonic acid (AMPS) were obtained by plasma-initiated copolymerization in water solution. The effects of plasma parameters include discharge time and discharge power on the intrinsic viscosity ([η]) of synthesized copolymers were studied. The copolymers were characterized by proton nuclear magnetic resonance spectroscopy (1H-NMR) and fourier transform infrared spectroscopy (FTIR) methods. The thermal behaviour of copolymers was also investigated by thermogravimetric analysis (TGA). The results of [η] measurements as function of discharge power indicated an optimum of 27.12 dl/g at 150W of discharge power and after that [η] started to decrease. Also the measurements of [η] for different discharge time were carried out and showed an optimum of 26.03 dl/g at 30s of discharge time. The TG data showed two stages of the weight loss which the first one occurred between 270°C and 330°C, with a weight loss about 40%, and the second one happened between 350°C and 460°C, with a weight loss about 25%, respectively. The presented results show that the produced copolymers are suitable for application in enhanced oil recovery process.
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