{"title":"噻虫胺吸附TiO2及珍珠岩负载TiO2的动力学和热力学研究","authors":"Emmanuel Ngaha, Dilek Duranoğlu","doi":"10.1007/s11144-025-02827-x","DOIUrl":null,"url":null,"abstract":"<div><p>Adsorption of thiamethoxam onto TiO<sub>2</sub> and perlite supported TiO<sub>2</sub> composite (PST) was investigated at different contact time and temperature (295 and 318 K). Adsorption kinetic was evaluated by using the Lindstrom adsorption model to obtain the rate constants of adsorption (k<sub>1</sub>) and desorption (k<sub>2</sub>) simultaneously. Thermodynamic parameters of adsorption like activation energy (∆E<sub>a</sub>), Gibbs free energy (∆G<sub>a</sub>), enthalpy (∆H<sub>a</sub>), and entropy (∆S<sub>a</sub>) were also calculated. The adsorption progressively increased with the contact time until equilibrium was achieved, except with PST (295 K), where almost 81% of the THX was eliminated during the initial 10 min. Equilibrium was reached after 35 min for TiO<sub>2</sub> and PST at any temperatures. The endothermic nature of the adsorption reaction of THX onto TiO<sub>2</sub> and PST has been highlighted. The modeling of the adsorption process allowed us to obtain the theoretical expression of THX adsorbed fraction (φ(t)) and then the adsorption (k<sub>1)</sub> and desorption (k<sub>1</sub>) rate constant. Adsorption was faster than desorption and spontaneously occurred, unlike desorption, which was non-spontaneous.</p></div>","PeriodicalId":750,"journal":{"name":"Reaction Kinetics, Mechanisms and Catalysis","volume":"138 4","pages":"2613 - 2626"},"PeriodicalIF":1.7000,"publicationDate":"2025-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Kinetics and thermodynamics study on thiamethoxam adsorption onto TiO2 and perlite supported TiO2\",\"authors\":\"Emmanuel Ngaha, Dilek Duranoğlu\",\"doi\":\"10.1007/s11144-025-02827-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Adsorption of thiamethoxam onto TiO<sub>2</sub> and perlite supported TiO<sub>2</sub> composite (PST) was investigated at different contact time and temperature (295 and 318 K). Adsorption kinetic was evaluated by using the Lindstrom adsorption model to obtain the rate constants of adsorption (k<sub>1</sub>) and desorption (k<sub>2</sub>) simultaneously. Thermodynamic parameters of adsorption like activation energy (∆E<sub>a</sub>), Gibbs free energy (∆G<sub>a</sub>), enthalpy (∆H<sub>a</sub>), and entropy (∆S<sub>a</sub>) were also calculated. The adsorption progressively increased with the contact time until equilibrium was achieved, except with PST (295 K), where almost 81% of the THX was eliminated during the initial 10 min. Equilibrium was reached after 35 min for TiO<sub>2</sub> and PST at any temperatures. The endothermic nature of the adsorption reaction of THX onto TiO<sub>2</sub> and PST has been highlighted. The modeling of the adsorption process allowed us to obtain the theoretical expression of THX adsorbed fraction (φ(t)) and then the adsorption (k<sub>1)</sub> and desorption (k<sub>1</sub>) rate constant. Adsorption was faster than desorption and spontaneously occurred, unlike desorption, which was non-spontaneous.</p></div>\",\"PeriodicalId\":750,\"journal\":{\"name\":\"Reaction Kinetics, Mechanisms and Catalysis\",\"volume\":\"138 4\",\"pages\":\"2613 - 2626\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2025-03-15\",\"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/s11144-025-02827-x\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reaction Kinetics, Mechanisms and Catalysis","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11144-025-02827-x","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Kinetics and thermodynamics study on thiamethoxam adsorption onto TiO2 and perlite supported TiO2
Adsorption of thiamethoxam onto TiO2 and perlite supported TiO2 composite (PST) was investigated at different contact time and temperature (295 and 318 K). Adsorption kinetic was evaluated by using the Lindstrom adsorption model to obtain the rate constants of adsorption (k1) and desorption (k2) simultaneously. Thermodynamic parameters of adsorption like activation energy (∆Ea), Gibbs free energy (∆Ga), enthalpy (∆Ha), and entropy (∆Sa) were also calculated. The adsorption progressively increased with the contact time until equilibrium was achieved, except with PST (295 K), where almost 81% of the THX was eliminated during the initial 10 min. Equilibrium was reached after 35 min for TiO2 and PST at any temperatures. The endothermic nature of the adsorption reaction of THX onto TiO2 and PST has been highlighted. The modeling of the adsorption process allowed us to obtain the theoretical expression of THX adsorbed fraction (φ(t)) and then the adsorption (k1) and desorption (k1) rate constant. Adsorption was faster than desorption and spontaneously occurred, unlike desorption, which was non-spontaneous.
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.