TY - JOUR
T1 - Solid peroxides in Fenton-like reactions at near neutral pHs
T2 - Superior performance of MgO2 on the accelerated reduction of ferric species
AU - Zhu, Yitong
AU - Qin, Jiaolong
AU - Zhang, Shuqi
AU - Radian, Adi
AU - Long, Mingce
N1 - Funding Information: This work was supported by the National Key Research and Development Program of China ( 2017YFE0195800 ), the National Natural Science Foundation of China ( 21876108 ) and Shanghai Municipal International Cooperation Foundation ( 19230713800 ). The authors also acknowledge the experimental support of the BET-BJH analysis from Ms. Jie Zhang of Instrumental Analysis Center of Shanghai Jiao Tong University. Publisher Copyright: © 2020 Elsevier Ltd Copyright: Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020
Y1 - 2020
N2 - Fenton-like reactions at near neutral pHs are limited by the slow reduction of ferric species. Enhancing generation of [Formula presented] from solid peroxides is a promising strategy to accelerate the rate-limiting step. Herein, the H2O2 release and Fenton-like reactions of four solid peroxides, MgO2, CaO2, ZnO2 and urea hydrogen peroxide (UHP), were investigated. Results indicated that UHP can release H2O2 instantly and show a similar behavior as H2O2 in the Fenton-like reactions. MgO2 released H2O2 quickly in phosphate buffered solutions, which was comparable to CaO2 but faster than ZnO2. Metal peroxides induced higher initial phenol degradation rates than UHP and H2O2 when the same theoretic H2O2 dosages and Fe(III)-EDTA were used. MgO2 displayed a superior performance for phenol degradation at pH 5, resulting in more than 93% phenol reduction at 1.5 h. According to kinetic analyses, the generation rate of [Formula presented] in the MgO2 system was 18 and 3.4 times higher than those in ZnO2 and CaO2 systems, respectively. The addition of MgO2 significantly promoted H2O2 based Fenton-like reactions by increasing production of [Formula presented], and the mixture of MgO2 and H2O2 had an improved utilization efficiency of active oxygen than the MgO2 system. The findings suggested the critical roles of metal peroxides in favoring Fenton-like reactions and inspired strategies to simultaneously accelerate Fenton-like reactions and improve utilization efficiency of active oxygen.
AB - Fenton-like reactions at near neutral pHs are limited by the slow reduction of ferric species. Enhancing generation of [Formula presented] from solid peroxides is a promising strategy to accelerate the rate-limiting step. Herein, the H2O2 release and Fenton-like reactions of four solid peroxides, MgO2, CaO2, ZnO2 and urea hydrogen peroxide (UHP), were investigated. Results indicated that UHP can release H2O2 instantly and show a similar behavior as H2O2 in the Fenton-like reactions. MgO2 released H2O2 quickly in phosphate buffered solutions, which was comparable to CaO2 but faster than ZnO2. Metal peroxides induced higher initial phenol degradation rates than UHP and H2O2 when the same theoretic H2O2 dosages and Fe(III)-EDTA were used. MgO2 displayed a superior performance for phenol degradation at pH 5, resulting in more than 93% phenol reduction at 1.5 h. According to kinetic analyses, the generation rate of [Formula presented] in the MgO2 system was 18 and 3.4 times higher than those in ZnO2 and CaO2 systems, respectively. The addition of MgO2 significantly promoted H2O2 based Fenton-like reactions by increasing production of [Formula presented], and the mixture of MgO2 and H2O2 had an improved utilization efficiency of active oxygen than the MgO2 system. The findings suggested the critical roles of metal peroxides in favoring Fenton-like reactions and inspired strategies to simultaneously accelerate Fenton-like reactions and improve utilization efficiency of active oxygen.
KW - Fenton-like reactions
KW - Magnesium peroxide
KW - Solid peroxides
KW - Superoxide radical
KW - Utilization efficiency
UR - http://www.scopus.com/inward/record.url?scp=85093915199&partnerID=8YFLogxK
U2 - 10.1016/j.chemosphere.2020.128639
DO - 10.1016/j.chemosphere.2020.128639
M3 - مقالة
SN - 0045-6535
VL - 270
JO - Chemosphere
JF - Chemosphere
M1 - 128639
ER -