New composites of nanoparticle Cu (I) oxide and titania in a novel inorganic polymer (geopolymer) matrix for destruction of dyes and hazardous organic pollutants

被引:83
作者
Falah, Mahroo [1 ]
MacKenzie, Kenneth J. D. [1 ]
Knibbe, Ruth [2 ]
Page, Samuel J. [3 ]
Hanna, John V. [3 ]
机构
[1] Victoria Univ Wellington, Sch Chem & Phys Sci, MacDiarmid Inst Adv Mat & Nanotechnol, Wellington, New Zealand
[2] Victoria Univ Wellington, Robinson Res Inst, Wellington, New Zealand
[3] Univ Warwick, Dept Phys, Coventry CV4 7AL, W Midlands, England
关键词
Photocatalysis; TiO2/Cu2O nanoparticles; Modified geopolymers; Organic pollutants; AQUEOUS-SOLUTION; CUPROUS-OXIDE; MONTMORILLONITE;
D O I
10.1016/j.jhazmat.2016.06.016
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
New photoactive composites to efficiently remove organic dyes from water are reported. These consist of Cu2O/TiO2 nanoparticles in a novel inorganic geopolymer matrix modified by a large tertiary ammonium species (cetyltrimethylammonium bromide, CTAB) whose presence in the matrix is demonstrated by FTIR spectroscopy. The CTAB does not disrupt the tetrahedral geopolymer structural silica and alumina units as demonstrated by Si-29 and Al-27 MAS NMR spectroscopy. SEM/EDS, TEM and BET measurements suggest that the Cu2O/TiO2 nanoparticles are homogenously distributed on the surface and within the geopolymer pores. The mechanism of removal of methylene blue (MB) dye from solution consists of a combination of adsorption (under dark conditions) and photodegradation (under UV radiation). MB adsorption in the dark follows pseudo second-order kinetics and is described by Freundlich-Langmuir type isotherms. The performance of the CTAB-modified geopolymer based composites is superior to composites based on unmodified geopolymer hosts, the most effective composite containing 5 wt% Cu2O/TiO2 in a CTAB-modified geopolymer host. These composites constitute a new class of materials with excellent potential in environmental protection applications. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:772 / 782
页数:11
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