Electrospinning of multifunctional cellulose acetate membrane and its adsorption properties for ionic dyes

被引:92
作者
Chen, Wenjuan [1 ]
Ma, Hongzhu [1 ,2 ]
Xing, Baoshan [2 ]
机构
[1] Shaanxi Normal Univ, Sch Chem & Chem Engn, Key Lab Appl Surface & Colloid Chem, Minist Educ, Xian 710119, Shaanxi, Peoples R China
[2] Univ Massachusetts, Stockbridge Sch Agr, Amherst, MA 01003 USA
关键词
Cellulose acetate; Electrospinning; Surface modification; Coating; Adsorption; CONGO RED-DYE; METHYLENE-BLUE; EFFECTIVE ADSORBENT; AQUEOUS-SOLUTION; ORGANIC-DYES; WASTE-WATER; REMOVAL; COMPOSITE; ACID; EQUILIBRIUM;
D O I
10.1016/j.ijbiomac.2020.04.249
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Electrospinning of cellulose acetate with appropriated solvent system is the most straightforward method for fabricating micro-and nanofibers. To simultaneously and effectively remove both cationic and anionic dyes, a novel cost-effective multifunctional cellulose acetate (CA) fibers membrane was prepared by electrospinning followed by deacetylation, carboxymethylation and polydopamine (PDA) coating. The adsorption properties of PDA@DCA-COOH membrane were evaluated with methylene blue (MB) and Congo red (CR) as the ionic repre-sentatives for their removal. The results indicated that carboxyl, hydroxyl and amine multifunctional groups had been successfully grafted on the surface of the nanofibers with the maximum adsorption capacities of 69.89 and 67.31 mg g(-1) for MB and CR, respectively, in the individual systems. The effect of co-existed dyes, inorganic salts and surfactants on the uptake of MB and CR in the simulated real complex system was strongly depended on the initial pH and ionic strength of the solution. The excellent adsorption capacities of the composite membrane were due to strong electrostatic attraction through the abundant functional groups on PDA@DCA-COOH surface. Based on its excellent recycling performance and adsorption property, PDA@DCA-COOH has a promising potential as an effective adsorbent in water treatment. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:1342 / 1351
页数:10
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