Tìm kiếm theo cụm từ
Chi tiết
Tên Heterogeneous catalyst ozonation of Direct Black 22 from aqueous solution in the presence of metal slags originating from industrial solid wastes
Lĩnh vực Tài nguyên-Môi trường
Tác giả Huu Tap Van,Xuan Hoa Vu, Van Tuyen Trinh, Thi Hong Vien Nguyen, Thi Dong Nguyen, Tien Vinh Nguyen, Lan Huong Nguyen, N.T. Hien, Thi Hong Huyen Chu
Nhà xuất bản / Tạp chí Separation and Purification Technology Năm 2019
Số hiệu ISSN/ISBN Separation and Purification Technology
Tóm tắt nội dung

This study developed a low cost catalyst, namely, zinc slag (Zn-S) for the ozonation process of Direct Black 22 (DB22) from aqueous solutions. Among five different kind of low cost metal slags including Fe-S, Cu-S, Cd-S, Pb-S and Zn-S, the Zn-S slag was selected as an efficient catalyst in this study. Zn-S contained mainly zinc (Zn) and calcium (Ca) discharged from zinc slag waste in Vietnam. It was found that Zn-S could effectively decolonize and mineralize DB22 through heterogeneous catalytic ozonation. The degradation kinetic of DB22 followed the pseudo-first order model. The best removal efficiency of DB22 (Zn-S/O3/H2O2 (76%) > Zn-S/O3 (69%) > O3/H2O2 (66%) > O3 (55% for COD) occurred at pH 11 for heterogeneous catalytic ozonation processes with Zn-S as the catalyst as well as ozone alone and perozone processes due to fast decomposition of O3 in alkaline solution to generate powerful and non-selective OH radicals. An increase in decolonization and mineralization rate was observed when increasing the Zn-S dosage from 0.125 g/L to 0.75 g/L for Zn-S/O3 and 0.125 g/L to 1.0 g/L for Zn-S/O3/H2O2. The K values of the pseudo-first order model followed the same sequence as mineralization rates of DB22 in term of COD removal. Ca and Zn constituents in the Zn-S catalyst contributed to the increase in O3 decomposition and improvement of reaction rate with H2O2. Subsequently, the degradation of DB22 by the ozonation process with Zn-S catalyst was enhanced through the enrichment mechanism of hydroxyl radicals (*OH) and surface adsorption. The degradation mechanism of DB22 by hydroxyl radicals was surely affirmed by tests with the decrease in degradation percentage of DB22 in case of the presence t-butanol, Cl− and CO32−.