...
首页> 外文期刊>Journal of Macromolecular Science. Pure and Applied Chemistry >Poly(acrylamide-co-itaconic acid) as a potential ion-exchange sorbent for effective removal of antibiotic drug-ciprofloxacin from aqueous solution
【24h】

Poly(acrylamide-co-itaconic acid) as a potential ion-exchange sorbent for effective removal of antibiotic drug-ciprofloxacin from aqueous solution

机译:聚丙烯酰胺-衣康酸作为潜在的离子交换吸附剂,可有效去除水溶液中的抗生素药物环丙沙星

获取原文
获取原文并翻译 | 示例
           

摘要

This study describes equilibrium and kinetic sorption studies to remove the antibiotic drug Ciprofloxacin (CF) from aqueous solutions using poly(acrylamide-co-itaconic acid) [poly(AAm-co-IA)] as polymeric cation exchanger sorbent material. The co-polymeric sorbent was prepared by free radical induced aqueous polymerization and was characterized by FTIR spectroscopy and TGA analysis. In addition, its physicochemical parameters were also determined. The various isotherm models, when applied to equilibrium sorption data at 28°C, followed the following order: Langmuir > Temkin > Freundlich, with the fair maximum sorption capacity (Qo) of 178.5 mg g-1. The kinetic sorption data, obtained at 28°C, was applied to kinetic models such as pseudo first order equation, pseudo second order model and a simple Elovich model. Based on regression values, the order of fitness of these models was pseudo second order > pseudo first order > simple Elovich model. The second order adsorption coefficients k2ads were found to be 58 × 10~(-3), 52.7 × 10~(-3), 34.01 × 10~(-3) g/mg min for drug solutions with initial concentrations of 10, 20 and 30 mg L-1 respectively The sorption mean free energy from the Dubinin-Raduschkevich (DR) isotherm was found to be nearly 8.839 kJ mol-1 indicating an ion-exchange mechanism for drug uptake. The optimum pH value of sorbate solution for drug uptake was found to be around 6.0. Finally, the antibacterial action of drug was investigated and it was found that after adsorption there was a decrease in bacterial growth inhibition efficiency of drug solution.
机译:这项研究描述了平衡和动力学吸附研究,该研究使用聚(丙烯酰胺-衣康酸)[聚(AAm-co-IA)]作为聚合阳离子交换吸附剂材料从水溶液中去除抗生素环丙沙星(CF)。通过自由基诱导的水性聚合反应制备共聚物吸附剂,并通过FTIR光谱和TGA分析对其进行表征。此外,还确定了其理化参数。将各种等温线模型应用于28°C的平衡吸附数据时,应遵循以下顺序:Langmuir> Temkin> Freundlich,其最大吸附量(Qo)为178.5 mg g-1。将在28°C下获得的动力学吸附数据应用于动力学模型,例如伪一级方程,伪二级模型和简单的Elovich模型。基于回归值,这些模型的适应度顺序为伪二阶>伪一阶>简单Elovich模型。初始浓度为10、20的药物溶液的二阶吸附系数k2ads为58×10〜(-3),52.7×10〜(-3),34.01×10〜(-3)g / mg min分别为30 mg L-1和30 mg L-1。来自Dubinin-Raduschkevich(DR)等温线的吸附平均自由能接近8.839 kJ mol-1,表明药物吸收的离子交换机制。发现用于药物吸收的山梨酸盐溶液的最佳pH值为约6.0。最后,研究了药物的抗菌作用,发现吸附后药物溶液的细菌生长抑制效率降低。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号