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Synthesization, characterization and adsorption properties of sulfonic cellulose

纤维素 磺酸 吸附 硝酸铈铵 阳离子聚合 化学 傅里叶变换红外光谱 核化学 无机化学 高分子化学 有机化学 化学工程 嫁接 聚合物 工程类
作者
Wenjian Shi,Yan Zhou,Yuanzhang Zhang,Liang Li,Qinlin Yang
出处
期刊:Water Science and Technology [Pergamon Press]
卷期号:66 (12): 2638-2646 被引量:5
标识
DOI:10.2166/wst.2012.493
摘要

The synthesization and characterization of a new environmental functional material–sulfonic cellulose – were studied in this paper. The preparation conditions were optimized through an orthogonal experiment. The modified cellulose was characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and scanning electron microscope (SEM). The adsorption rules of cationic organic pollutants and heavy metal ions by this new material were discussed. Regeneration and recycling performances of the sulfonic cellulose were also investigated. At the temperature of 323 K, sulfonic cellulose was prepared by grafting 2-acrylamido-2-methylpropane sulfonic acid (AMPS) onto alkali-treated cellulose for 4 h with the employing of ceric ammonium nitrate as initiator. The mass ratio of AMPS to cellulose was 3:1 and the concentration of ceric ammonium nitrate was 63.8 mmol/L. The sulfur content of sulfonic cellulose was 7.32 wt%. The peaks of 1,303 and 1,159 cm−1 in IR suggested the existence of the sulfonic group in sulfonic cellulose. The XRD and SEM results showed that the crystallinity decreased while the specific surface area increased after modification. Batch adsorption results showed that sulfonic cellulose had a favorable adsorption capacity for model contaminants at pH 6.0–7.0. The adsorption process was endothermic and reached equilibrium in 180 min. The adsorption rules of cationic organic pollutants and heavy metal ions indicated that sulfonic cellulose had high adsorption capacity for the cationic dyes with a coplanar macromolecule structure and organic compounds carrying the amino group. Under room temperature, 1.0 mol/L HCl can be used as a desorption solution and the equilibrium adsorption capacity had little decrease (less than 7%) after six adsorption–desorption cycles.
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