{"title":"具有高效光催化性能的可见光活性ti3 +自掺杂介孔tio2光催化剂降解毒死蜱","authors":"Mansour Sarafraz, Ramin Khaghani, Mohsen Ebrahimi, Alireza Khajeh-Amiri","doi":"10.1080/03067319.2023.2282714","DOIUrl":null,"url":null,"abstract":"ABSTRACTIn the present research, Ti3+ self-doped TiO2 photocatalyst (Ti3+-TiO2) was fabricated through a facial in-situ NaBH4 reduction approach. The as-prepared Ti3+-TiO2 were characterised using FESEM-EDS, TEM, HRTEM, XRD, UV-DRS, PL, EIS, and BET methods. The photocatalytic performance of the Ti3+-TiO2 was assessed through the degradation of chlorpyrifos (CPY) as an organophosphorus pesticide under visible LED light irradiation. The Ti3+-TiO2 exhibited excellent photocatalytic degradation efficiency at initial CIP concentration = 1 mg L−1, pH = 7, catalyst dosage = 0.2 g L−1, and reaction time of 50 min with 97%, which is 4.62 times higher than that of pristine TiO2. The extraordinarily boosted photocatalytic activity of Ti3+-TiO2 can be attributed to mesoporous nanostructure, oxygen vacancy, and Ti3+ self-doping, which facilitates visible light harvesting and accelerates charge carrier separation and transport. In addition, Ti3+-TiO2 shows outstanding mineralisation capability and recycling performance in degrading CPY. Coexisting water anions (NO3−, Cl−, SO4 2-, HCO3−) and HA inhibited the degradation of CPY. Their inhibition effects of selected anions followed the order of HCO3− > SO4 2-> NO3− > Cl−. Besides, a possible reaction mechanism of the photocatalytic process was recommended based on evidence from the radical scavenging test and photoelectrochemical measurements. The energy consumption value in this study was much less than that reported in other studies. Collectively, the findings show that Ti3+-TiO2 photocatalyst has tremendous potential in solar photocatalytic degradation of refractory organic pollutants.KEYWORDS: Visible-light-driven photocatalysiselectron–hole pairTi3+ self-doped TiO2energy consumption AcknowledgmentsThe present study was adopted from the project of Mansour Sarafraz at Aja University of Medical Sciences with 1400.213 project number. We are very grateful to Aja University of Medical Sciences for its financial and equipment support.Disclosure statementNo potential conflict of interest was reported by the author(s).Additional informationFundingThis work was supported by the Aja University of Medical Sciences.","PeriodicalId":13973,"journal":{"name":"International Journal of Environmental Analytical Chemistry","volume":"18 7","pages":"0"},"PeriodicalIF":2.3000,"publicationDate":"2023-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Visible light active Ti <sup>3+</sup> self-doped mesoporous TiO <sub>2</sub> photocatalyst with efficient photocatalytic performance for the degradation of chlorpyrifos\",\"authors\":\"Mansour Sarafraz, Ramin Khaghani, Mohsen Ebrahimi, Alireza Khajeh-Amiri\",\"doi\":\"10.1080/03067319.2023.2282714\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"ABSTRACTIn the present research, Ti3+ self-doped TiO2 photocatalyst (Ti3+-TiO2) was fabricated through a facial in-situ NaBH4 reduction approach. The as-prepared Ti3+-TiO2 were characterised using FESEM-EDS, TEM, HRTEM, XRD, UV-DRS, PL, EIS, and BET methods. The photocatalytic performance of the Ti3+-TiO2 was assessed through the degradation of chlorpyrifos (CPY) as an organophosphorus pesticide under visible LED light irradiation. The Ti3+-TiO2 exhibited excellent photocatalytic degradation efficiency at initial CIP concentration = 1 mg L−1, pH = 7, catalyst dosage = 0.2 g L−1, and reaction time of 50 min with 97%, which is 4.62 times higher than that of pristine TiO2. The extraordinarily boosted photocatalytic activity of Ti3+-TiO2 can be attributed to mesoporous nanostructure, oxygen vacancy, and Ti3+ self-doping, which facilitates visible light harvesting and accelerates charge carrier separation and transport. In addition, Ti3+-TiO2 shows outstanding mineralisation capability and recycling performance in degrading CPY. Coexisting water anions (NO3−, Cl−, SO4 2-, HCO3−) and HA inhibited the degradation of CPY. Their inhibition effects of selected anions followed the order of HCO3− > SO4 2-> NO3− > Cl−. Besides, a possible reaction mechanism of the photocatalytic process was recommended based on evidence from the radical scavenging test and photoelectrochemical measurements. The energy consumption value in this study was much less than that reported in other studies. Collectively, the findings show that Ti3+-TiO2 photocatalyst has tremendous potential in solar photocatalytic degradation of refractory organic pollutants.KEYWORDS: Visible-light-driven photocatalysiselectron–hole pairTi3+ self-doped TiO2energy consumption AcknowledgmentsThe present study was adopted from the project of Mansour Sarafraz at Aja University of Medical Sciences with 1400.213 project number. We are very grateful to Aja University of Medical Sciences for its financial and equipment support.Disclosure statementNo potential conflict of interest was reported by the author(s).Additional informationFundingThis work was supported by the Aja University of Medical Sciences.\",\"PeriodicalId\":13973,\"journal\":{\"name\":\"International Journal of Environmental Analytical Chemistry\",\"volume\":\"18 7\",\"pages\":\"0\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2023-11-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Environmental Analytical Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/03067319.2023.2282714\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Environmental Analytical Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/03067319.2023.2282714","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Visible light active Ti 3+ self-doped mesoporous TiO 2 photocatalyst with efficient photocatalytic performance for the degradation of chlorpyrifos
ABSTRACTIn the present research, Ti3+ self-doped TiO2 photocatalyst (Ti3+-TiO2) was fabricated through a facial in-situ NaBH4 reduction approach. The as-prepared Ti3+-TiO2 were characterised using FESEM-EDS, TEM, HRTEM, XRD, UV-DRS, PL, EIS, and BET methods. The photocatalytic performance of the Ti3+-TiO2 was assessed through the degradation of chlorpyrifos (CPY) as an organophosphorus pesticide under visible LED light irradiation. The Ti3+-TiO2 exhibited excellent photocatalytic degradation efficiency at initial CIP concentration = 1 mg L−1, pH = 7, catalyst dosage = 0.2 g L−1, and reaction time of 50 min with 97%, which is 4.62 times higher than that of pristine TiO2. The extraordinarily boosted photocatalytic activity of Ti3+-TiO2 can be attributed to mesoporous nanostructure, oxygen vacancy, and Ti3+ self-doping, which facilitates visible light harvesting and accelerates charge carrier separation and transport. In addition, Ti3+-TiO2 shows outstanding mineralisation capability and recycling performance in degrading CPY. Coexisting water anions (NO3−, Cl−, SO4 2-, HCO3−) and HA inhibited the degradation of CPY. Their inhibition effects of selected anions followed the order of HCO3− > SO4 2-> NO3− > Cl−. Besides, a possible reaction mechanism of the photocatalytic process was recommended based on evidence from the radical scavenging test and photoelectrochemical measurements. The energy consumption value in this study was much less than that reported in other studies. Collectively, the findings show that Ti3+-TiO2 photocatalyst has tremendous potential in solar photocatalytic degradation of refractory organic pollutants.KEYWORDS: Visible-light-driven photocatalysiselectron–hole pairTi3+ self-doped TiO2energy consumption AcknowledgmentsThe present study was adopted from the project of Mansour Sarafraz at Aja University of Medical Sciences with 1400.213 project number. We are very grateful to Aja University of Medical Sciences for its financial and equipment support.Disclosure statementNo potential conflict of interest was reported by the author(s).Additional informationFundingThis work was supported by the Aja University of Medical Sciences.
期刊介绍:
International Journal of Environmental Analytical Chemistry comprises original research on all aspects of analytical work related to environmental problems. This includes analysis of organic, inorganic and radioactive pollutants in air, water, sediments and biota; and determination of harmful substances, including analytical methods for the investigation of chemical or metabolic breakdown patterns in the environment and in biological samples.
The journal also covers the development of new analytical methods or improvement of existing ones useful for the control and investigation of pollutants or trace amounts of naturally occurring active chemicals in all environmental compartments. Development, modification and automation of instruments and techniques with potential in environment sciences are also part of the journal.
Case studies are also considered, particularly for areas where information is scarce or lacking, providing that reported data is significant and representative, either spatially or temporally, and quality assured. Owing to the interdisciplinary nature of this journal, it will also include topics of interest to researchers in the fields of medical science (health sciences), toxicology, forensic sciences, oceanography, food sciences, biological sciences and other fields that, in one way or another, contribute to the knowledge of our environment and have to make use of analytical chemistry for this purpose.