Lourdes A. Etshindo , Célia Sousa , Priscila Tamiasso-Martinhon , Marcos V. Colaço , Alexandre R. Camara , Angela S. Rocha
{"title":"紫外和可见光下光催化降解阳离子染料的 SnO2-TiO2 材料及壳聚糖复合膜研究","authors":"Lourdes A. Etshindo , Célia Sousa , Priscila Tamiasso-Martinhon , Marcos V. Colaço , Alexandre R. Camara , Angela S. Rocha","doi":"10.1016/j.cattod.2024.114995","DOIUrl":null,"url":null,"abstract":"<div><p>The possibility of SnO<sub>2</sub> incorporation and immobilization as films forming composites opens new perspectives for TiO<sub>2</sub> to profit visible light and to facilitate the photocatalytic process, respectively. In this study, 0 %, 1 % and 10 % wt. of SnO<sub>2</sub> was incorporated into TiO<sub>2</sub> (SnO<sub>2</sub>-TiO<sub>2</sub>) by coprecipitation in a sol-gel method by ammonia addition, followed for calcination at 500 °C. The photocatalysts were characterized by N<sub>2</sub> adsorption-desorption, FTIR spectroscopy, XRD Rietveld refinement, TG-DTG, SEM-EDS, DRS and elemental analysis. The performance of all solids was evaluated in the photocatalytic degradation of the cationic dye methylene blue in aqueous phase, under visible and UV irradiation, at 25 °C for 2 h. The results showed that the incorporation of Sn into TiO<sub>2</sub> improved the textural properties and decreased the bandgap. All solids presented only TiO<sub>2</sub> typical diffractograms, with anatase as the main phase, but catalyst with 10 % SnO<sub>2</sub> presented also brookite phase, inferring that Sn atoms were incorporated into TiO<sub>2</sub> structure, corroborated by MEV results. All tin-based photocatalysts show high activity under UV and visible light, with the 10 % SnO<sub>2</sub> material reaching 83 % and 88 % degradation after 2 h under UV and visible radiation, respectively. This material was tested as an immobilized film, achieving 14 % of decolorization, and the reuse was also evaluated. Our investigation demonstrates that SnO<sub>2</sub>-TiO<sub>2</sub> catalysts could be used to decompose a dye under UV and Visible light as powder in a batch reactor and immobilized as a composite film with chitosan, that opens new perspectives to facilitate the application using solar light.</p></div>","PeriodicalId":264,"journal":{"name":"Catalysis Today","volume":"444 ","pages":"Article 114995"},"PeriodicalIF":5.2000,"publicationDate":"2024-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"SnO2-TiO2 materials for photocatalytic degradation of cationic dye under UV and visible light and a chitosan composite film investigation\",\"authors\":\"Lourdes A. Etshindo , Célia Sousa , Priscila Tamiasso-Martinhon , Marcos V. Colaço , Alexandre R. Camara , Angela S. Rocha\",\"doi\":\"10.1016/j.cattod.2024.114995\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The possibility of SnO<sub>2</sub> incorporation and immobilization as films forming composites opens new perspectives for TiO<sub>2</sub> to profit visible light and to facilitate the photocatalytic process, respectively. In this study, 0 %, 1 % and 10 % wt. of SnO<sub>2</sub> was incorporated into TiO<sub>2</sub> (SnO<sub>2</sub>-TiO<sub>2</sub>) by coprecipitation in a sol-gel method by ammonia addition, followed for calcination at 500 °C. The photocatalysts were characterized by N<sub>2</sub> adsorption-desorption, FTIR spectroscopy, XRD Rietveld refinement, TG-DTG, SEM-EDS, DRS and elemental analysis. The performance of all solids was evaluated in the photocatalytic degradation of the cationic dye methylene blue in aqueous phase, under visible and UV irradiation, at 25 °C for 2 h. The results showed that the incorporation of Sn into TiO<sub>2</sub> improved the textural properties and decreased the bandgap. All solids presented only TiO<sub>2</sub> typical diffractograms, with anatase as the main phase, but catalyst with 10 % SnO<sub>2</sub> presented also brookite phase, inferring that Sn atoms were incorporated into TiO<sub>2</sub> structure, corroborated by MEV results. All tin-based photocatalysts show high activity under UV and visible light, with the 10 % SnO<sub>2</sub> material reaching 83 % and 88 % degradation after 2 h under UV and visible radiation, respectively. This material was tested as an immobilized film, achieving 14 % of decolorization, and the reuse was also evaluated. Our investigation demonstrates that SnO<sub>2</sub>-TiO<sub>2</sub> catalysts could be used to decompose a dye under UV and Visible light as powder in a batch reactor and immobilized as a composite film with chitosan, that opens new perspectives to facilitate the application using solar light.</p></div>\",\"PeriodicalId\":264,\"journal\":{\"name\":\"Catalysis Today\",\"volume\":\"444 \",\"pages\":\"Article 114995\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2024-08-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Catalysis Today\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0920586124004899\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Today","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0920586124004899","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
SnO2-TiO2 materials for photocatalytic degradation of cationic dye under UV and visible light and a chitosan composite film investigation
The possibility of SnO2 incorporation and immobilization as films forming composites opens new perspectives for TiO2 to profit visible light and to facilitate the photocatalytic process, respectively. In this study, 0 %, 1 % and 10 % wt. of SnO2 was incorporated into TiO2 (SnO2-TiO2) by coprecipitation in a sol-gel method by ammonia addition, followed for calcination at 500 °C. The photocatalysts were characterized by N2 adsorption-desorption, FTIR spectroscopy, XRD Rietveld refinement, TG-DTG, SEM-EDS, DRS and elemental analysis. The performance of all solids was evaluated in the photocatalytic degradation of the cationic dye methylene blue in aqueous phase, under visible and UV irradiation, at 25 °C for 2 h. The results showed that the incorporation of Sn into TiO2 improved the textural properties and decreased the bandgap. All solids presented only TiO2 typical diffractograms, with anatase as the main phase, but catalyst with 10 % SnO2 presented also brookite phase, inferring that Sn atoms were incorporated into TiO2 structure, corroborated by MEV results. All tin-based photocatalysts show high activity under UV and visible light, with the 10 % SnO2 material reaching 83 % and 88 % degradation after 2 h under UV and visible radiation, respectively. This material was tested as an immobilized film, achieving 14 % of decolorization, and the reuse was also evaluated. Our investigation demonstrates that SnO2-TiO2 catalysts could be used to decompose a dye under UV and Visible light as powder in a batch reactor and immobilized as a composite film with chitosan, that opens new perspectives to facilitate the application using solar light.
期刊介绍:
Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues.
Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.