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通过表面引发原子转移自由基聚合对再生纤维素膜进行功能化,用于从水溶液中去除硼。

Functionalization of regenerated cellulose membrane via surface initiated atom transfer radical polymerization for boron removal from aqueous solution.

机构信息

Department of Civil and Environmental Engineering, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260.

出版信息

Langmuir. 2011 May 17;27(10):6018-25. doi: 10.1021/la200154y. Epub 2011 Apr 21.

Abstract

In this study, an adsorptive membrane was prepared for efficient boron removal. Poly(glycidyl methacrylate) was grafted on the surfaces of the regenerated cellulose (RC) membrane via surface-initiated atom transfer radical polymerization, and N-methylglucamine was used to further react with epoxide rings to introduce polyhydroxyl functional groups, which served as the major binding sites for boron. The pristine and modified membranes were characterized by X-ray photoelectron spectroscopy (XPS), attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR), dynamic water contact angle measurement, and scanning electron microscopy. It was shown that the designed functional groups were successfully grafted onto the RC membrane, and surface modification contributed to higher boron binding capability. The optimal pH range for boron adsorption was 4-8. Under a neutral pH condition, the maximum adsorption capacity of the modified membrane was determined to be 0.75 mmol/g, which was comparable with those of commercial resins. Studies of electrolyte influence indicated the formation of inner-sphere surface complexes on the membrane surface. The ATR-FTIR and XPS analyses showed that secondary alcohol and tertiary amine groups were mainly involved in boron adsorption, and tetrahedral boron complexes were found on the membrane surface.

摘要

本研究制备了一种吸附膜,用于高效去除硼。通过表面引发原子转移自由基聚合,将聚(甲基丙烯酸缩水甘油酯)接枝在再生纤维素(RC)膜表面上,然后用 N-甲基葡糖胺进一步与环氧化物反应,引入多羟基官能团,作为硼的主要结合位点。用 X 射线光电子能谱(XPS)、衰减全反射傅里叶变换红外光谱(ATR-FTIR)、动态水接触角测量和扫描电子显微镜对原始和改性膜进行了表征。结果表明,设计的官能团成功地接枝到 RC 膜上,表面改性有助于提高硼的结合能力。硼吸附的最佳 pH 范围为 4-8。在中性 pH 条件下,改性膜的最大吸附容量为 0.75mmol/g,与商业树脂相当。电解质影响研究表明,在膜表面形成了内球表面配合物。ATR-FTIR 和 XPS 分析表明,二级醇和三级胺基团主要参与硼吸附,并且在膜表面发现了四面体硼配合物。

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