Magnetically separable and recyclable Fe3O4-polydopamine hybrid hollow microsphere for highly efficient peroxidase mimetic catalysts

被引:59
作者
Liu, Shujun [1 ]
Fu, Jianwei [1 ]
Wang, Minghuan [1 ]
Yan, Ya [1 ]
Xin, Qianqian [1 ]
Cai, Lu [1 ]
Xu, Qun [1 ]
机构
[1] Zhengzhou Univ, Sch Mat Sci & Engn, 75 Daxue Rd, Zhengzhou 450052, Peoples R China
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
Polydopamine; Fe3O4; Incorporated; Hollow microspheres; Peroxidase-like; Catalyst; Stability; SUPERPARAMAGNETIC FE3O4 NANOPARTICLES; WATER-PURIFICATION; FACILE SYNTHESIS; SPHERES; GRAPHENE; OXIDE; NANOCOMPOSITES; ANTIBACTERIAL; DELIVERY; ROUTE;
D O I
10.1016/j.jcis.2016.02.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Magnetic Fe3O4-polydopamine (PDA) hybrid hollow microspheres, in which Fe3O4 nanoparticles were firmly incorporated in the cross-linked PDA shell, have been prepared through the formation of core/shell PS/Fe3O4-PDA composites based on template-induced covalent assembly method, followed by core removal in a tetrahydrofuran solution. The morphology, composition, thermal property and magnetic property of the magnetic hybrid hollow microspheres were characterized by SEM, TEM, FT-IR, XRD, TGA, and vibrating sample magnetometer, respectively. Results revealed that the magnetic hybrid hollow microspheres had about 380 nm of inner diameter and about 30 nm of shell thickness, and 13.6 emu g(-1) of magnetization saturation. More importantly, the Fe3O4-PDA hybrid hollow microspheres exhibited intrinsic peroxidase-like activity, as they could quickly catalyze the oxidation of typical substrates 3,3', 5,5'-tetramethylbenzidine (TMB) in the presence of hydrogen peroxide. Compared with PDA/Fe3O4 composites where Fe3O4 nanoparticles were loaded on the surface of PDA microspheres, the stability of Fe3O4-PDA hybrid hollow microspheres was greatly improved. As-prepared magnetic hollow micro spheres might open up a new application field in biodetection, biocatalysis, and environmental monitoring. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:69 / 77
页数:9
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