Effectiveness and mechanism of cyanide remediation from contaminated soils using thermally activated persulfate

Chemosphere ◽  
2021 ◽  
pp. 133463
Author(s):  
Yunmei Wei ◽  
Shuang Chen ◽  
Tingting Ren ◽  
Lianying Chen ◽  
Yuanyuan Liu ◽  
...  
2021 ◽  
Vol 412 ◽  
pp. 128624
Author(s):  
Tian-Lin Ren ◽  
Xi-Wen Ma ◽  
Xiao-Qiong Wu ◽  
Li Yuan ◽  
Yang-Li Lai ◽  
...  

2011 ◽  
Vol 50 (19) ◽  
pp. 11029-11036 ◽  
Author(s):  
Xiaogang Gu ◽  
Shuguang Lu ◽  
Lin Li ◽  
Zhaofu Qiu ◽  
Qian Sui ◽  
...  

2016 ◽  
Vol 92 (6) ◽  
pp. 1192-1202 ◽  
Author(s):  
Isil Akmehmet Balcioglu ◽  
Nalan Bilgin Oncu ◽  
Nazire Mercan

2015 ◽  
Vol 286 ◽  
pp. 7-14 ◽  
Author(s):  
Minhui Xu ◽  
Xiaogang Gu ◽  
Shuguang Lu ◽  
Zhaofu Qiu ◽  
Qian Sui ◽  
...  

2019 ◽  
Vol 2019 ◽  
pp. 1-10 ◽  
Author(s):  
Juanjuan Zhao ◽  
Yujiao Sun ◽  
Fachao Wu ◽  
Minjian Shi ◽  
Xurui Liu

Antibiotic residues and antibiotic resistance genes (ARGs) pose a great threat to public health and food security via the horizontal transfer in the food production chain. Oxidative degradation of amoxicillin (AMO) in aqueous solution by thermally activated persulfate (TAP) was investigated. The AMO degradation followed a pseudo-first-order kinetic model at all tested conditions. The pseudo-first-order rate constants of AMO degradation well-fitted the Arrhenius equation when the reaction temperature ranged from 35°C to 60°C, with the apparent activate energy of 126.9 kJ·mol−1. High reaction temperature, high initial persulfate concentration, low pH, high Cl− concentration, and humic acid (HA) concentration increased the AMO degradation efficiency. The EPR test demonstrated that both ·OH and SO4·− were generated in the TAP system, and the radical scavenging test identified that the predominant reactive radical species were SO4·− in aqueous solution without adjusting the solution pH. In groundwater and drinking water, AMO degradation suggested that TAP could be a reliable technology for water remediation contaminated by AMO in practice.


2017 ◽  
Vol 75 (8) ◽  
pp. 1794-1803 ◽  
Author(s):  
Jialu Liu ◽  
Zhehua Liu ◽  
Fengjun Zhang ◽  
Xiaosi Su ◽  
Cong Lyu

This study investigates the interaction of persulfate with soil components and chlorinated volatile organic compounds (CVOCs), using thermally activated persulfate oxidation in three soil types: high sand content; high clay content; and paddy field soil. The effect of soil composition on the available oxidant demand and CVOC removal rate was evaluated. Results suggest that the treatment efficiency of CVOCs in soil can be ranked as follows: cis-1,2-dichloroethene > trichloroethylene > 1,2-dichloroethane > 1,1,1-trichloroethane. The reactions of soil components with persulfate, shown by the reduction in soil phase natural organics and mineral content, occurred in parallel with persulfate oxidation of CVOCs. Natural oxidant demand from the reaction of soil components with persulfate exerted a large relative contribution to the total oxidant demand. The main influencing factor in oxidant demand in paddy-soil-persulfate systems was natural organics, rather than mineral content as seen with sand and clay soil types exposed to the persulfate system. The competition between CVOCs and soil components for oxidation by persulfate indicates that soil composition exhibits a considerable influence on the available oxidant demand and CVOC removal efficiency. Therefore, soil composition of natural organics and mineral content is a critical factor in estimating the oxidation efficiency of in-situ remediation systems.


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