首页|真空紫外活化亚氯酸盐降解酸性红G的机理

真空紫外活化亚氯酸盐降解酸性红G的机理

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采用真空紫外(VUV)活化亚氯酸盐(Cl02-),研究其对偶氮染料酸性红G(ARG)的氧化降解机理,考察不同体系、ClO2-浓度、初始pH值、ARG初始浓度、无机阴离子和印染助剂对ARG降解效能的影响.结果表明:在ARG初始质量浓度为50 mg/L、ClO2-投加浓度为0.4 mmol/L的条件下,反应10 min时,VUV/ClO2-体系中ARG去除率可达98.3%.ARG去除速率随pH值的增大而降低,Cl-会促进ARG氧化分解,HCO3-有微弱的抑制作用,NO3-、SO42-影响较小,柠檬酸钠和十二烷基苯磺酸钠抑制作用显著.VUV/ClO2-体系中主要氧化物质为·OH、1O2、Cl·和ClO·,ARG降解机理为偶氮键断裂和萘环被破坏.
Mechanism of Acid Red G Degradation by VUV-activated Chlorite
The oxidative degradation mechanism of azo dye acid red G by vacuum ultraviolet(VUV)activa-ted chlorite(ClO2-)was studied,and the effects of different systems,ClO2-concentration,initial pH value,ini-tial concentration of acid red G,inorganic anions,printing and dyeing auxiliaries on the degradation efficiency of acid red G were explored.The results showed that when the initial mass concentration of acid red G was 50 mg/L,the concentration of ClO2-was 0.4 mmol/L and the reaction time was 10 min,the removal rate of acid red G in VUV/ClO2-system could reach 98.3%.The removal rate of ARG decreased with the increase of pH value.Cl-promoted the oxidative decomposition of ARG.HCO3-had a weak inhibitory effect,while NO3-and SO42-had a minor impact.Sodium citrate and SDBS had a significant inhibitory effect.The main oxidizing sub-stances in VUV/ClO2-system were·OH,1O2,Cl·and ClO·.The mechanism of ARG degradation was the fracture of azo bond and the destruction of naphthalene ring.

Acidic red GVUVChloriteActive radicalOxidation degradation

朱先胜、唐玉朝、伍昌年、黄显怀、王坤、陈徐庆、陈彩虹

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安徽建筑大学,环境污染控制与资源化安徽省重点实验室,安徽 合肥 230601

酸性红G 真空紫外 亚氯酸盐 活性自由基 氧化降解

国家自然科学基金资助项目安徽省自然科学基金资助项目安徽省教育厅创新团队基金资助项目

532700212208085US202022AH010019

2024

环境监测管理与技术
江苏省环境监测中心,南京市环境监测中心站

环境监测管理与技术

CSTPCD北大核心
影响因子:1.086
ISSN:1006-2009
年,卷(期):2024.36(5)
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