{"title":"Bi3+和Fe3+共掺杂纳米羟基磷灰石作为可见光驱动下降解甲基橙的有效光催化剂","authors":"Dagne Bayih Adamu, Enyew Zereffa, Teshome Abdo Segne","doi":"10.1007/s11696-025-03940-w","DOIUrl":null,"url":null,"abstract":"<div><p>One of the major issues facing the world today is water contamination. The substitution of metal ions in the hydroxyapatite structure enhances its application for water treatment. Thus, this work applied Bi<sup>3+</sup> and Fe<sup>3+</sup> co-doped hydroxyapatite nanomaterials for the investigation of methyl orange dye photocatalytic degradation. Incorporations of Bi<sup>3+</sup> and Fe<sup>3+</sup> ions in the HA structure dramatically changed the light absorption property and the optical bandgap, due to the occurrence of the different electronic transitions of the dopant ions. In addition, the modification brings change in crystallite as well as particle size of HA nanomaterial. Elemental composition analysis inferred that the Ca/P ratio decreased as the dopants were introduced in the crystal system, which confirms direct replacement of Ca<sup>2+</sup> ions. The co-doped HA nanomaterials showed better photocatalytic degradation of MO dye over the pristine HA due to the synergistic roles of Fe<sup>3+</sup> and Bi<sup>3+</sup> ions. It was observed that 98.57% methyl orange was degraded at 180 min of irradiation time using 0.6 g/L of the nanomaterial. Thus, Bi<sup>3+</sup> and Fe<sup>3+</sup> co-doped HA nanomaterials can be considered competent heterogeneous photocatalysts for the degradation of azo dyes.</p></div>","PeriodicalId":513,"journal":{"name":"Chemical Papers","volume":"79 4","pages":"2437 - 2452"},"PeriodicalIF":2.2000,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bi3+ and Fe3+ Co-doped nanohydroxyapatite as an effective photocatalyst driven by visible light for methyl orange degradation\",\"authors\":\"Dagne Bayih Adamu, Enyew Zereffa, Teshome Abdo Segne\",\"doi\":\"10.1007/s11696-025-03940-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>One of the major issues facing the world today is water contamination. The substitution of metal ions in the hydroxyapatite structure enhances its application for water treatment. Thus, this work applied Bi<sup>3+</sup> and Fe<sup>3+</sup> co-doped hydroxyapatite nanomaterials for the investigation of methyl orange dye photocatalytic degradation. Incorporations of Bi<sup>3+</sup> and Fe<sup>3+</sup> ions in the HA structure dramatically changed the light absorption property and the optical bandgap, due to the occurrence of the different electronic transitions of the dopant ions. In addition, the modification brings change in crystallite as well as particle size of HA nanomaterial. Elemental composition analysis inferred that the Ca/P ratio decreased as the dopants were introduced in the crystal system, which confirms direct replacement of Ca<sup>2+</sup> ions. The co-doped HA nanomaterials showed better photocatalytic degradation of MO dye over the pristine HA due to the synergistic roles of Fe<sup>3+</sup> and Bi<sup>3+</sup> ions. It was observed that 98.57% methyl orange was degraded at 180 min of irradiation time using 0.6 g/L of the nanomaterial. Thus, Bi<sup>3+</sup> and Fe<sup>3+</sup> co-doped HA nanomaterials can be considered competent heterogeneous photocatalysts for the degradation of azo dyes.</p></div>\",\"PeriodicalId\":513,\"journal\":{\"name\":\"Chemical Papers\",\"volume\":\"79 4\",\"pages\":\"2437 - 2452\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-02-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Papers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11696-025-03940-w\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Engineering\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Papers","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11696-025-03940-w","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Engineering","Score":null,"Total":0}
Bi3+ and Fe3+ Co-doped nanohydroxyapatite as an effective photocatalyst driven by visible light for methyl orange degradation
One of the major issues facing the world today is water contamination. The substitution of metal ions in the hydroxyapatite structure enhances its application for water treatment. Thus, this work applied Bi3+ and Fe3+ co-doped hydroxyapatite nanomaterials for the investigation of methyl orange dye photocatalytic degradation. Incorporations of Bi3+ and Fe3+ ions in the HA structure dramatically changed the light absorption property and the optical bandgap, due to the occurrence of the different electronic transitions of the dopant ions. In addition, the modification brings change in crystallite as well as particle size of HA nanomaterial. Elemental composition analysis inferred that the Ca/P ratio decreased as the dopants were introduced in the crystal system, which confirms direct replacement of Ca2+ ions. The co-doped HA nanomaterials showed better photocatalytic degradation of MO dye over the pristine HA due to the synergistic roles of Fe3+ and Bi3+ ions. It was observed that 98.57% methyl orange was degraded at 180 min of irradiation time using 0.6 g/L of the nanomaterial. Thus, Bi3+ and Fe3+ co-doped HA nanomaterials can be considered competent heterogeneous photocatalysts for the degradation of azo dyes.
Chemical PapersChemical Engineering-General Chemical Engineering
CiteScore
3.30
自引率
4.50%
发文量
590
期刊介绍:
Chemical Papers is a peer-reviewed, international journal devoted to basic and applied chemical research. It has a broad scope covering the chemical sciences, but favors interdisciplinary research and studies that bring chemistry together with other disciplines.