Functionalization of cellulose nanofiber mats with phthalocyanine for decoloration of reactive dye wastewater

被引:49
作者
Chen, Shi-Liang [1 ,2 ]
Huang, Xiao-Jun [1 ]
Xu, Zhi-Kang [1 ]
机构
[1] Zhejiang Univ, MOE Key Lab Macromol Synth & Functionalizat, Dept Polymer Sci & Engn, Hangzhou 310027, Zhejiang, Peoples R China
[2] Hangzhou Normal Univ, Qianjiang Coll, Hangzhou 310012, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Cellulose acetate; Nanofiber mats; Phthalocyanine; Immobilization; Decoloration; IRON TETRASULFOPHTHALOCYANINE; METAL-COMPLEXES; OXIDATION; CATALYSTS; NANOCOMPOSITES; DEGRADATION; ACETATE; SURFACE;
D O I
10.1007/s10570-011-9572-5
中图分类号
TB3 [工程材料学]; TS [轻工业、手工业、生活服务业];
学科分类号
0805 ; 080502 ; 0822 ;
摘要
A versatile method is reported for the preparation of cellulose nanofiber mats immobilized with cobalt tetraaminophthalocyanine (CoPc). This functionalized cellulose nanomaterial was used as an efficient catalyst for the decoloration of reactive dye wastewater. Cellulose acetate was electrospun into nanofiber mats (CA-NM), hydrolyzed with KOH, and then oxidized by NaIO(4) to generate aldehyde groups for CoPc immobilization. The functionalization processes on the nanofiber mats were monitored by attenuated total reflection Fourier transform infrared spectroscopy (ATR/FT-IR), X-ray photoelectron spectroscopy (XPS), and field emission scanning electron microscope (FESEM). We found these CoPc-functionalized nanofiber mats (CoPc-NM) have high adsorption capacity for reactive dye from synthetic wastewater, which enhances the catalytic oxidation rate of reactive dye when H(2)O(2) is present as oxidant. More than 90% of reactive red X-3B can be eliminated by CoPc-NM/H(2)O(2) in 90 min. UV and GC-MS analyses indicate the catalytic oxidation not only breaking the azo linkages but also decomposing the aromatic parts of reactive red X-3B, and the main products are biodegradable aliphatic acids, such as fumaric acid, succinic acid, and maleic acid, etc. Repetitive measurements also show that this CoPc-NM is quite stable and remains efficient with no obvious decrease of catalytic activity.
引用
收藏
页码:1295 / 1303
页数:9
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