Sara K. Saeed , Duaa H. Altamer , Ahmed M. Khalaf , Abdelrahman B. Fadhil
{"title":"在 K2CO3 活性生物炭上超声辅助吸附脱硫模型燃料中的二苯并噻吩","authors":"Sara K. Saeed , Duaa H. Altamer , Ahmed M. Khalaf , Abdelrahman B. Fadhil","doi":"10.1016/j.cep.2024.110065","DOIUrl":null,"url":null,"abstract":"<div><div>A novel mesoporous activated biochar (ABC) was developed from an equal mix of date and olive stones and implemented in the ultrasound-assisted adsorptive desulfurization (USADS) of model gasoline (300 ppm DBT/n-hexane) and model kerosene (300 ppm DBT/cyclohexane). The biowaste blend was carbonized at 450 °C for 75 min at a 10 °C/min heating rate, followed by K<sub>2</sub>CO<sub>3</sub>-activation. The superior ABC was synthesized at 750 °C for 1 h using an impregnation ratio of 1:1 K<sub>2</sub>CO<sub>3</sub>: biochar. The BET surface area and average pore diameter of the resulting ABC were 1099.70 m<sup>2</sup>/g and 5.14 nm, respectively. The USADS of both models was achieved at relatively mild experimental conditions (0.20 g of the ABC 30 °C, 40 min, and 120 W US power). At these conditions, the USADS of model gasoline amounted to 97.32 % compared to 99.39 % for model kerosene. The USADS process of both models followed the Langmuir model of the adsorption isotherms and the pseudo-2nd-order kinetics model. The ABC was recoverable and effective until the 5th regeneration cycle and reused reasonably. The maximum USADS of real gasoline (88.12 %) was achieved using 1.0 g of the ABC at 30 °C for 120 min.</div></div>","PeriodicalId":9929,"journal":{"name":"Chemical Engineering and Processing - Process Intensification","volume":"206 ","pages":"Article 110065"},"PeriodicalIF":3.8000,"publicationDate":"2024-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ultrasound-assisted adsorptive desulfurization of dibenzothiophene from model fuel on K2CO3-activated biochar\",\"authors\":\"Sara K. Saeed , Duaa H. Altamer , Ahmed M. Khalaf , Abdelrahman B. Fadhil\",\"doi\":\"10.1016/j.cep.2024.110065\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A novel mesoporous activated biochar (ABC) was developed from an equal mix of date and olive stones and implemented in the ultrasound-assisted adsorptive desulfurization (USADS) of model gasoline (300 ppm DBT/n-hexane) and model kerosene (300 ppm DBT/cyclohexane). The biowaste blend was carbonized at 450 °C for 75 min at a 10 °C/min heating rate, followed by K<sub>2</sub>CO<sub>3</sub>-activation. The superior ABC was synthesized at 750 °C for 1 h using an impregnation ratio of 1:1 K<sub>2</sub>CO<sub>3</sub>: biochar. The BET surface area and average pore diameter of the resulting ABC were 1099.70 m<sup>2</sup>/g and 5.14 nm, respectively. The USADS of both models was achieved at relatively mild experimental conditions (0.20 g of the ABC 30 °C, 40 min, and 120 W US power). At these conditions, the USADS of model gasoline amounted to 97.32 % compared to 99.39 % for model kerosene. The USADS process of both models followed the Langmuir model of the adsorption isotherms and the pseudo-2nd-order kinetics model. The ABC was recoverable and effective until the 5th regeneration cycle and reused reasonably. The maximum USADS of real gasoline (88.12 %) was achieved using 1.0 g of the ABC at 30 °C for 120 min.</div></div>\",\"PeriodicalId\":9929,\"journal\":{\"name\":\"Chemical Engineering and Processing - Process Intensification\",\"volume\":\"206 \",\"pages\":\"Article 110065\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2024-11-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Engineering and Processing - Process Intensification\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0255270124004033\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ENERGY & FUELS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Engineering and Processing - Process Intensification","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0255270124004033","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
Ultrasound-assisted adsorptive desulfurization of dibenzothiophene from model fuel on K2CO3-activated biochar
A novel mesoporous activated biochar (ABC) was developed from an equal mix of date and olive stones and implemented in the ultrasound-assisted adsorptive desulfurization (USADS) of model gasoline (300 ppm DBT/n-hexane) and model kerosene (300 ppm DBT/cyclohexane). The biowaste blend was carbonized at 450 °C for 75 min at a 10 °C/min heating rate, followed by K2CO3-activation. The superior ABC was synthesized at 750 °C for 1 h using an impregnation ratio of 1:1 K2CO3: biochar. The BET surface area and average pore diameter of the resulting ABC were 1099.70 m2/g and 5.14 nm, respectively. The USADS of both models was achieved at relatively mild experimental conditions (0.20 g of the ABC 30 °C, 40 min, and 120 W US power). At these conditions, the USADS of model gasoline amounted to 97.32 % compared to 99.39 % for model kerosene. The USADS process of both models followed the Langmuir model of the adsorption isotherms and the pseudo-2nd-order kinetics model. The ABC was recoverable and effective until the 5th regeneration cycle and reused reasonably. The maximum USADS of real gasoline (88.12 %) was achieved using 1.0 g of the ABC at 30 °C for 120 min.
期刊介绍:
Chemical Engineering and Processing: Process Intensification is intended for practicing researchers in industry and academia, working in the field of Process Engineering and related to the subject of Process Intensification.Articles published in the Journal demonstrate how novel discoveries, developments and theories in the field of Process Engineering and in particular Process Intensification may be used for analysis and design of innovative equipment and processing methods with substantially improved sustainability, efficiency and environmental performance.