Natural cellulose fiber derived hollow-tubular-oriented polydopamine: In-situ formation of Ag nanoparticles for reduction of 4-nitrophenol

被引:58
作者
Cao, Enjuan [1 ]
Duan, Wenzhen [1 ]
Wang, Feng [2 ]
Wang, Aiqin [2 ]
Zheng, Yian [1 ,3 ]
机构
[1] Lanzhou Univ, Coll Earth & Environm Sci, Gansu Key Lab Environm Pollut Predict & Control, Lanzhou 730000, Peoples R China
[2] Chinese Acad Sci, Lanzhou Inst Chem Phys, Ctr Ecomat & Green Chem, Lanzhou 730000, Peoples R China
[3] Lanzhou Univ, Zhongwei High Tech Inst, Zhongwei 755000, Peoples R China
基金
中国国家自然科学基金;
关键词
Kapok fiber; Calotropis gigantea fiber; Polydopamine; In-situ reduction; 4-Nitrophenol; DISPERSED SILVER NANOPARTICLES; STABILIZED GOLD NANOPARTICLES; CALOTROPIS-GIGANTEA FIBER; CATALYTIC-REDUCTION; KAPOK FIBER; FACILE SYNTHESIS; POLYANILINE NANOFIBERS; SOUND-ABSORPTION; GRAPHENE OXIDE; COMPOSITE;
D O I
10.1016/j.carbpol.2016.12.004
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A facile method was reported to achieve hollow-tubular-oriented polydopamine (HTO-PDA) layer using natural kapok fiber (KF) as the bio-template without any pretreatments by altering hydrophobic fiber into hydrophilic one. Subsequently, the HTO-PDA can be utilized for direct in-situ deposition of Ag nanoparticles (NPs). The structures of pristine fiber and HTO-PDA, as well as the resulting Ag NPs attached HTO-PDA (Ag@HTO-PDA) were well characterized by means of scanning electron microscopy (SEM) coupled energy dispersion spectrum (EDS), x-ray diffraction (XRD), transmission electron microscopy (TEM), thermogravimetric analysis (TGA) and Fourier transform infrared (FTIR) spectroscopy. Due to the presence of relatively uniform Ag NPs attached onto PDA layer, Ag@KF-HTO-PDA shows stable catalytic ability towards the reduction of 4-nitrophenol into its amino derivative. Further, this method was used for facile fabrication of Calotropis gigantea fiber derived, surface-functionalized material. The experimental data demonstrated also its excellent catalytic efficiency towards 4-nitrophenol reduction. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:44 / 50
页数:7
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