过硫酸盐
电子顺磁共振
吸附
核化学
苯胺
化学
催化作用
四环素
激活剂(遗传学)
降级(电信)
材料科学
化学工程
无机化学
物理化学
有机化学
物理
工程类
基因
电信
生物化学
抗生素
核磁共振
计算机科学
作者
Junxia Chen,Zhenzhen Yang,Weigang Li,Yuying Yang,Feng Zhu,Zongli Huo,Qing Zhou
出处
期刊:Research Square - Research Square
日期:2023-12-27
标识
DOI:10.21203/rs.3.rs-3618197/v1
摘要
Abstract The poor conductivity, poor stability and agglomeration of MIL-88A(Fe) limit its application as persulfate (PS) activator in water purification. Herein, MXene-supported MIL-88A (Fe) composites (M88A/MX) were synthesized to enhance its adsorption and catalytic capability for tetracycline (TC) removal. M88A/MX-0.2 composites exhibits optimal degradation efficiency,reaching 98% under conditions of 0.2 g/L M88A/MX-0.2, 1.0 mM PS, 20 ppm TC, and pH 5. The degradation rate constants of M88A/MX-0.2 was 0.03217 min -1 , which was much higher than that of MIL-88A(Fe) (0.00159 min -1 ) and MXene (0.00626 min -1 ). The removal effects of reaction parameters, such as dosage of M88A/MX-0.2 and PS, initial solution pH and the presence of the common co-existing constituents (humic acid and the inorganic anions) were investigated in detail. Additionally, the reuse of M88A/MX-0.2 showed that the composites had good cycling stability. The results of electron paramagnetic resonance (EPR) and quenching experiments indicated that ·OH, ·SO 4 - and ·O 2 - were involved in the M88A/MX-0.2/PS system. This study offered a new avenue for sulfate-based degradation of Fe-based metal organic framework.
科研通智能强力驱动
Strongly Powered by AbleSci AI