4.5 Article

Optimization and mechanism of Acid Orange 7 removal by powdered activated carbon coupled with persulfate by response surface method

期刊

WATER SCIENCE AND TECHNOLOGY
卷 79, 期 6, 页码 1195-1205

出版社

IWA PUBLISHING
DOI: 10.2166/wst.2019.117

关键词

peroxydisulfate; powder activated carbon; reaction mechanism; response surface method

资金

  1. Fundamental Research Funds for the Central Universities of China [2018CDYJSY0055]
  2. National Natural Science Foundation of China [51308563]
  3. Graduate Research and Innovation Foundation of Chongqing of China [CYS18030]
  4. Frontier Interdisciplinary Training Project of Fundamental Research Funds for the Central Universities of China [2018CDQYCH0053]

向作者/读者索取更多资源

In this study, powder activated carbon (PAC) utilized to activate peroxydisulfate (PDS) was investigated for decolorization of Acid Orange 7 (AO7). The results indicated a remarkable synergistic effect in the PAC/PDS system. The effect of PAC, PDS dosages and initial pH on AO7 decolorization were studied and the processes followed first-order kinetics. Response surface method with central composite design (CCD) model was utilized to optimize these three factors and analyze the combined interaction. The optimum condition for the decolorization rate of AO7 was analyzed as the following: PAC (0.19 g/L), PDS (1.64 g/L), and initial pH (4.14). Cl- and SO42- showed a promoting effect on AO7 decolorization while HCO3- had a slightly inhibiting effect. Quenching experiments confirmed that both sulfate and hydroxyl radicals were the oxidizing species, and the oxidation reaction occurred on the surface of PAC. The results of UV-vis spectrum with 100% decolorization rate and the 50% total organic carbon reduction indicated highly efficient decolorization and mineralization of AO7 in the PAC/PDS system. Finally, the recovery performance of PAC was studied and the result indicated PAC had poor reuse in reactivity.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据