Yasmine Laftani, Baylassane Chatib, A. Boussaoud, M. Hachkar, Mohammed El Makhfouk
{"title":"UV/过氧酸盐和UV/过硫酸盐氧化法对比光降解染料废水","authors":"Yasmine Laftani, Baylassane Chatib, A. Boussaoud, M. Hachkar, Mohammed El Makhfouk","doi":"10.2166/wqrj.2022.012","DOIUrl":null,"url":null,"abstract":"\n Generation of anion sulfate radicals (SO4•−) and hydroxyl radicals (HO•) by UV/Persulfate and the UV/Peroxydate processes have been successfully studied to degrade Ponceau S dye. Under [PS] = 0.06 mM; [H2O2] = 2 mM; [S2O82-] = 2 mM, the UV/Persulfate process was effective (kapp = 0.163 min−1) than the UV/Peroxydate process (kapp = 0.054 min−1). The lack of dissolved oxygen, the excess of hydrogen peroxide (H2O2) dosage at 2 mM, and the alkaline pH of 10.01 significantly reduced the UV/Peroxydate efficiency. The scavenging effect of the hydrogenocarbonates and nitrates on the PS dye degradation by the UV/Persulfate process was significant, whereas chlorides had a slight influence. The composition of seawater in chlorides, sulfates, carbonates, and bromides decreased the photoactivity of the studied processes. The presence of phenol showed that the reactive affinity of the (HO•) is more superior to the SO4•−. The UV/Persulfate process achieved 82.35% of chemical oxygen demand removal against 59.56% for the UV/Peroxydate in about 100 min. This study demonstrated that the UV/Persulfate process is a viable option for PS dye degradation. To the best of our knowledge, this is the first report for studying the PS dye degradation under some varying new operational factors. However, the identification of by-products, their nature, and their concentration requires special attention.","PeriodicalId":23720,"journal":{"name":"Water Quality Research Journal","volume":null,"pages":null},"PeriodicalIF":2.4000,"publicationDate":"2022-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Comparative photo-degradative treatment of dyeing industry wastewater containing diazo dye by UV/Peroxydate and UV/Persulfate − oxidation processes\",\"authors\":\"Yasmine Laftani, Baylassane Chatib, A. Boussaoud, M. Hachkar, Mohammed El Makhfouk\",\"doi\":\"10.2166/wqrj.2022.012\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n Generation of anion sulfate radicals (SO4•−) and hydroxyl radicals (HO•) by UV/Persulfate and the UV/Peroxydate processes have been successfully studied to degrade Ponceau S dye. Under [PS] = 0.06 mM; [H2O2] = 2 mM; [S2O82-] = 2 mM, the UV/Persulfate process was effective (kapp = 0.163 min−1) than the UV/Peroxydate process (kapp = 0.054 min−1). The lack of dissolved oxygen, the excess of hydrogen peroxide (H2O2) dosage at 2 mM, and the alkaline pH of 10.01 significantly reduced the UV/Peroxydate efficiency. The scavenging effect of the hydrogenocarbonates and nitrates on the PS dye degradation by the UV/Persulfate process was significant, whereas chlorides had a slight influence. The composition of seawater in chlorides, sulfates, carbonates, and bromides decreased the photoactivity of the studied processes. The presence of phenol showed that the reactive affinity of the (HO•) is more superior to the SO4•−. The UV/Persulfate process achieved 82.35% of chemical oxygen demand removal against 59.56% for the UV/Peroxydate in about 100 min. This study demonstrated that the UV/Persulfate process is a viable option for PS dye degradation. To the best of our knowledge, this is the first report for studying the PS dye degradation under some varying new operational factors. However, the identification of by-products, their nature, and their concentration requires special attention.\",\"PeriodicalId\":23720,\"journal\":{\"name\":\"Water Quality Research Journal\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2022-09-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Water Quality Research Journal\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://doi.org/10.2166/wqrj.2022.012\",\"RegionNum\":4,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"WATER RESOURCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Water Quality Research Journal","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.2166/wqrj.2022.012","RegionNum":4,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"WATER RESOURCES","Score":null,"Total":0}
Comparative photo-degradative treatment of dyeing industry wastewater containing diazo dye by UV/Peroxydate and UV/Persulfate − oxidation processes
Generation of anion sulfate radicals (SO4•−) and hydroxyl radicals (HO•) by UV/Persulfate and the UV/Peroxydate processes have been successfully studied to degrade Ponceau S dye. Under [PS] = 0.06 mM; [H2O2] = 2 mM; [S2O82-] = 2 mM, the UV/Persulfate process was effective (kapp = 0.163 min−1) than the UV/Peroxydate process (kapp = 0.054 min−1). The lack of dissolved oxygen, the excess of hydrogen peroxide (H2O2) dosage at 2 mM, and the alkaline pH of 10.01 significantly reduced the UV/Peroxydate efficiency. The scavenging effect of the hydrogenocarbonates and nitrates on the PS dye degradation by the UV/Persulfate process was significant, whereas chlorides had a slight influence. The composition of seawater in chlorides, sulfates, carbonates, and bromides decreased the photoactivity of the studied processes. The presence of phenol showed that the reactive affinity of the (HO•) is more superior to the SO4•−. The UV/Persulfate process achieved 82.35% of chemical oxygen demand removal against 59.56% for the UV/Peroxydate in about 100 min. This study demonstrated that the UV/Persulfate process is a viable option for PS dye degradation. To the best of our knowledge, this is the first report for studying the PS dye degradation under some varying new operational factors. However, the identification of by-products, their nature, and their concentration requires special attention.