Qingchun Yu , Shichao Zhang , Xindong Wang , Jie Zhang , Zhenming Lu
{"title":"CuO/γ-Al2O3吸附剂去除烟气中SO2的硫化行为","authors":"Qingchun Yu , Shichao Zhang , Xindong Wang , Jie Zhang , Zhenming Lu","doi":"10.1016/S1005-8850(08)60094-8","DOIUrl":null,"url":null,"abstract":"<div><p>CuO/γ-Al<sub>2</sub>O<sub>3</sub> has been considered as a promising and recycling sorbent to remove sulfur dioxide from flue gas. In this study, a series of CuO/γ-Al<sub>2</sub>O<sub>3</sub> sorbents with different CuO loadings were prepared by impregnation. The monolayer coverage of CuO supported on γ-Al<sub>2</sub>O<sub>3</sub> determined by X-ray quantitative analysis was 0.275 g CuO/g (γ-Al<sub>2</sub>O<sub>3</sub>). Below the monolayer coverage, CuO was found highly dispersed on γ-Al<sub>2</sub>O<sub>3</sub>. Thermogravimetric technique was used to study sulfation kinetics and sulfation recycling. It was found that the Langmuir kinetic adsorption model described well the experimental data at the rapid sulfation region of the CuO/γ-Al<sub>2</sub>O<sub>3</sub> sorbent. The adsorption activation energy was 19.98 kJ/mol and the pre-exponential factor was 9.97×10<sup>−5</sup> s<sup>−1</sup> · Pa<sup>−1</sup>. The CuO/γ-Al<sub>2</sub>O<sub>3</sub> sorbent has shown good performance on regeneration, but long sulfation time might cause the deactivation of the CuO/γ-Al<sub>2</sub>O<sub>3</sub> sorbent. It was also seen that the sulfated γ-Al<sub>2</sub>O<sub>3</sub> support could not be reduced at 400°C.</p></div>","PeriodicalId":100851,"journal":{"name":"Journal of University of Science and Technology Beijing, Mineral, Metallurgy, Material","volume":"15 4","pages":"Pages 500-504"},"PeriodicalIF":0.0000,"publicationDate":"2008-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1005-8850(08)60094-8","citationCount":"7","resultStr":"{\"title\":\"Sulfation behavior of CuO/γ-Al2O3 sorbent for the removal of SO2 from flue gas\",\"authors\":\"Qingchun Yu , Shichao Zhang , Xindong Wang , Jie Zhang , Zhenming Lu\",\"doi\":\"10.1016/S1005-8850(08)60094-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>CuO/γ-Al<sub>2</sub>O<sub>3</sub> has been considered as a promising and recycling sorbent to remove sulfur dioxide from flue gas. In this study, a series of CuO/γ-Al<sub>2</sub>O<sub>3</sub> sorbents with different CuO loadings were prepared by impregnation. The monolayer coverage of CuO supported on γ-Al<sub>2</sub>O<sub>3</sub> determined by X-ray quantitative analysis was 0.275 g CuO/g (γ-Al<sub>2</sub>O<sub>3</sub>). Below the monolayer coverage, CuO was found highly dispersed on γ-Al<sub>2</sub>O<sub>3</sub>. Thermogravimetric technique was used to study sulfation kinetics and sulfation recycling. It was found that the Langmuir kinetic adsorption model described well the experimental data at the rapid sulfation region of the CuO/γ-Al<sub>2</sub>O<sub>3</sub> sorbent. The adsorption activation energy was 19.98 kJ/mol and the pre-exponential factor was 9.97×10<sup>−5</sup> s<sup>−1</sup> · Pa<sup>−1</sup>. The CuO/γ-Al<sub>2</sub>O<sub>3</sub> sorbent has shown good performance on regeneration, but long sulfation time might cause the deactivation of the CuO/γ-Al<sub>2</sub>O<sub>3</sub> sorbent. It was also seen that the sulfated γ-Al<sub>2</sub>O<sub>3</sub> support could not be reduced at 400°C.</p></div>\",\"PeriodicalId\":100851,\"journal\":{\"name\":\"Journal of University of Science and Technology Beijing, Mineral, Metallurgy, Material\",\"volume\":\"15 4\",\"pages\":\"Pages 500-504\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2008-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S1005-8850(08)60094-8\",\"citationCount\":\"7\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of University of Science and Technology Beijing, Mineral, Metallurgy, Material\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1005885008600948\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of University of Science and Technology Beijing, Mineral, Metallurgy, Material","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1005885008600948","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7
摘要
CuO/γ-Al2O3被认为是一种很有前途的可循环利用的烟气脱硫吸附剂。本研究采用浸渍法制备了不同CuO负载量的CuO/γ-Al2O3吸附剂。通过x射线定量分析可知,γ-Al2O3上CuO的单层覆盖率为0.275 g CuO/g (γ-Al2O3)。在单层覆盖层下方,发现CuO高度分散在γ-Al2O3上。采用热重法研究了硫化动力学和硫化循环。结果表明,Langmuir动力学吸附模型较好地描述了CuO/γ-Al2O3吸附剂快速硫化区的实验数据。吸附活化能为19.98 kJ/mol,指前因子为9.97×10−5 s−1·Pa−1。CuO/γ-Al2O3吸附剂具有良好的再生性能,但磺化时间过长会导致吸附剂失活。在400℃时,硫酸酸化的γ-Al2O3载体不能被还原。
Sulfation behavior of CuO/γ-Al2O3 sorbent for the removal of SO2 from flue gas
CuO/γ-Al2O3 has been considered as a promising and recycling sorbent to remove sulfur dioxide from flue gas. In this study, a series of CuO/γ-Al2O3 sorbents with different CuO loadings were prepared by impregnation. The monolayer coverage of CuO supported on γ-Al2O3 determined by X-ray quantitative analysis was 0.275 g CuO/g (γ-Al2O3). Below the monolayer coverage, CuO was found highly dispersed on γ-Al2O3. Thermogravimetric technique was used to study sulfation kinetics and sulfation recycling. It was found that the Langmuir kinetic adsorption model described well the experimental data at the rapid sulfation region of the CuO/γ-Al2O3 sorbent. The adsorption activation energy was 19.98 kJ/mol and the pre-exponential factor was 9.97×10−5 s−1 · Pa−1. The CuO/γ-Al2O3 sorbent has shown good performance on regeneration, but long sulfation time might cause the deactivation of the CuO/γ-Al2O3 sorbent. It was also seen that the sulfated γ-Al2O3 support could not be reduced at 400°C.