Journal Home Online First Current Issue Archive For Authors Journal Information 中文版

Frontiers of Environmental Science & Engineering >> 2018, Volume 12, Issue 1 doi: 10.1007/s11783-017-1003-x

Degradation of Azo dye direct black BN based on adsorption and microwave-induced catalytic reaction

. State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210023, China.. School of Environment, Nanjing Normal University, Nanjing 210023, China

Available online: 2017-10-31

Next Previous

Abstract

The novel microwave catalyst MgFe O -SiC was synthesized via sol-gel method, to remove azo dye Direct Black BN (DB BN) through adsorption and microwave-induced catalytic reaction. Microwave-induced catalytic degradation of DB BN, including adsorption behavior and its influencing factors of DB BN on MgFe O -SiC were investigated. According to the obtained results, it indicated that the pseudo-second-order kinetics model was suitable for the adsorption of DB BN onto MgFe O -SiC. Besides, the consequence of adsorption isotherm depicted that the adsorption of DB BN was in accordance with the Langmuir isotherm, which verified that the singer layer adsorption of MgFe O -SiC was dominant than the multi-layer one. The excellent adsorption capacities of MgFe O -SiC were kept in the range of initial pH from 3 to 7. In addition, it could be concluded that the degradation rate of DB BN decreased over ten percent after the adsorption equilibrium had been attained, and the results from the result of comparative experiments manifested that the adsorption process was not conducive to the process of microwave-induced catalytic degradation. The degradation intermediates and products of DB BN were identified and determined by GC-MS and LC-MS. Furthermore, combined with the catalytic mechanism of MgFe O -SiC, the proposed degradation pathways of DB BN were the involution of microwave-induced ·OH and holes in this catalytic system the breakage of azo bond, hydroxyl substitution, hydroxyl addition, nitration reaction, deamination reaction, desorbate reaction, dehydroxy group and ring-opening reaction.

Related Research