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文章摘要
真空紫外活化亚氯酸盐降解酸性红G的机理
Mechanism of Acid Red G Degradation by VUV activated Chlorite
  
DOI:
中文关键词: 酸性红G  真空紫外  亚氯酸盐  活性自由基  氧化降解
英文关键词: Acidic red G  VUV  Chlorite  Active radical  Oxidation degradation
基金项目:国家自然科学基金资助项目(No53270021);安徽省自然科学基金资助项目(2208085US20);安徽省教育厅创新团队基金资助项目(2022AH010019)
作者单位
朱先胜 安徽建筑大学环境污染控制与资源化安徽省重点实验室 
唐玉朝 安徽建筑大学环境污染控制与资源化安徽省重点实验室 
伍昌年 安徽建筑大学环境污染控制与资源化安徽省重点实验室 
黄显怀 安徽建筑大学环境污染控制与资源化安徽省重点实验室 
王坤 安徽建筑大学环境污染控制与资源化安徽省重点实验室 
陈徐庆 安徽建筑大学环境污染控制与资源化安徽省重点实验室 
陈彩虹 安徽建筑大学环境污染控制与资源化安徽省重点实验室 
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中文摘要:
      采用真空紫外(VUV)活化亚氯酸盐(ClO-2),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、ClO-2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、ClO-2投加浓度为04mmol/L的条件下,反应10min时,VUV/ClO-2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,HCO-3有微弱的抑制作用,NO-3、SO2-4影响较小,柠檬酸钠和十二烷基苯磺酸钠抑制作用显著。VUV/ClO-2体系中主要氧化物质为·OH、1O2、Cl·和ClO·,ARG降解机理为偶氮键断裂和萘环被破坏。
英文摘要:
      The oxidative degradation mechanism of azo dye acid red G by vacuum ultraviolet(VUV) activated chlorite(ClO-2) was studied, and the effects of different systems, ClO-2 concentration, initial pH value, initial 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 ClO-2 was 04mmol/L and the reaction time was 10min, the removal rate of acid red G in VUV/ClO-2 system could reach 983% The removal rate of ARG decreased with the increase of pH value. Cl- promoted the oxidative decomposition of ARG HCO-3had a weak inhibitory effect, while NO-3 and SO2-4had aminor impact Sodium citrate and SDBS had a significant inhibitory effect The main oxidizing substances in VUV/ClO-2 system were ·OH,1O2, Cl·and ClO· The mechanism of ARG degradation was the fracture of azo bond and the destruction of naphthalene ring.
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