{"title":"Synthesis and characterization of novel bio-Ca doped Bi4Ti3O12 with the investigation of rhodamine-B removal under solar irradiation","authors":"Majda Charif, Hanane Rehali, Hayet Menasra, Chaima Benbrika, Loubna Sadaoui, Khadidja Hamida, Zineb Rais, Fedia Bekiri","doi":"10.1007/s11144-024-02766-z","DOIUrl":null,"url":null,"abstract":"<div><p>This study presents a novel approach for synthesizing high-performance Bi<sub>4</sub>Ti<sub>3</sub>O<sub>12</sub> trilayer-doped bio-calcium derived from snail shells using the molten salt technique at 850 °C. Three catalysts were prepared with varying amounts of bio-calcium (Bi<sub>(4−x)</sub>Ca<sub>x</sub>Ti<sub>3</sub>O<sub>12</sub>), where (x1 = 0.05, x 2 = 0.1, x3 = 0.15), it was observed that this activation led to an improvement in properties, the most important of which was an increase in the surface area and a reduction in the gap energy, resulting in excellent photocatalytic efficiency, particularly for biocatalysis with x3 = 0.15. The meticulous engineering of these catalysts gives rise to a synergistic effect, which facilitates efficient charge separation. Moreover, the introduction of bio-Ca led to an expansion in surface area, reaching 4.16, 5.42, and 6.03 m<sup>2</sup>/g for the bio-Ca/BTO1, bio-Ca/BTO2, and bio-Ca/BTO3, thereby augmenting the catalyst's capacity to absorb, stabilize and photodegradation of Rhodamine-B within a 30 min. Physical and chemical analyses were performed: XRD, FTIR, Raman analysis, BET, MEB/EDX. The bio-Ca/BTO3 photocatalyst’s unique structure enhances its performance and activity by stabilizing and degrading Rh-B on its surface, reducing band gaps, and producing electron–hole pairs. This increased vulnerability to photocatalytic reactions allows for a greater diversity of interactions. The ·OH radical was identified as the most active species in the Rh-B degradation mechanism. The biocatalyst demonstrated remarkable efficacy in degrading the Rh-B dye under visible light irradiation. To assess its stability, an additional eleven repeated simple cycles were conducted. This design offers a novel way to produce high-performance photocatalysts with, an environmentally friendly and sustainable approach.</p></div>","PeriodicalId":750,"journal":{"name":"Reaction Kinetics, Mechanisms and Catalysis","volume":"138 1","pages":"393 - 411"},"PeriodicalIF":1.7000,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reaction Kinetics, Mechanisms and Catalysis","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11144-024-02766-z","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
This study presents a novel approach for synthesizing high-performance Bi4Ti3O12 trilayer-doped bio-calcium derived from snail shells using the molten salt technique at 850 °C. Three catalysts were prepared with varying amounts of bio-calcium (Bi(4−x)CaxTi3O12), where (x1 = 0.05, x 2 = 0.1, x3 = 0.15), it was observed that this activation led to an improvement in properties, the most important of which was an increase in the surface area and a reduction in the gap energy, resulting in excellent photocatalytic efficiency, particularly for biocatalysis with x3 = 0.15. The meticulous engineering of these catalysts gives rise to a synergistic effect, which facilitates efficient charge separation. Moreover, the introduction of bio-Ca led to an expansion in surface area, reaching 4.16, 5.42, and 6.03 m2/g for the bio-Ca/BTO1, bio-Ca/BTO2, and bio-Ca/BTO3, thereby augmenting the catalyst's capacity to absorb, stabilize and photodegradation of Rhodamine-B within a 30 min. Physical and chemical analyses were performed: XRD, FTIR, Raman analysis, BET, MEB/EDX. The bio-Ca/BTO3 photocatalyst’s unique structure enhances its performance and activity by stabilizing and degrading Rh-B on its surface, reducing band gaps, and producing electron–hole pairs. This increased vulnerability to photocatalytic reactions allows for a greater diversity of interactions. The ·OH radical was identified as the most active species in the Rh-B degradation mechanism. The biocatalyst demonstrated remarkable efficacy in degrading the Rh-B dye under visible light irradiation. To assess its stability, an additional eleven repeated simple cycles were conducted. This design offers a novel way to produce high-performance photocatalysts with, an environmentally friendly and sustainable approach.
期刊介绍:
Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields:
-kinetics of homogeneous reactions in gas, liquid and solid phase;
-Homogeneous catalysis;
-Heterogeneous catalysis;
-Adsorption in heterogeneous catalysis;
-Transport processes related to reaction kinetics and catalysis;
-Preparation and study of catalysts;
-Reactors and apparatus.
Reaction Kinetics, Mechanisms and Catalysis was formerly published under the title Reaction Kinetics and Catalysis Letters.