Chaoyue Zhao , Wei Zhao , Yuan Ma , Yonghui Bai , Yuchen Li , Xudong Song , Jiaofei Wang , Peng Lv , Qinghua Guo , Guangsuo Yu , Min Yao
{"title":"磷诱导高硅铝高钙铁煤气化渣网络结构的聚合解聚机理","authors":"Chaoyue Zhao , Wei Zhao , Yuan Ma , Yonghui Bai , Yuchen Li , Xudong Song , Jiaofei Wang , Peng Lv , Qinghua Guo , Guangsuo Yu , Min Yao","doi":"10.1016/j.ces.2025.121738","DOIUrl":null,"url":null,"abstract":"<div><div>The flow behavior of slag during the co-gasification of phosphorus-containing wastes and coal is crucial for developing the co-treatment technology of phosphorus-containing wastes in the entrained flow gasification. In this work, high silica-alumina (Si-Al) and high calcium-iron (Ca-Fe) coal were used as reference materials, simplified to SiO<sub>2</sub>-Al<sub>2</sub>O<sub>3</sub>-CaO-Fe<sub>2</sub>O<sub>3</sub>. Synthetic ash was prepared with oxidizing reagents, and P<sub>2</sub>O<sub>5</sub> was added to study its impact on coal ash flow behavior and the phosphorus-induced polymerization-depolymerization mechanisms in the slag network structure. Results showed that P<sup>5+</sup> competed with Si<sup>4+</sup> for Al<sup>3+</sup> and O<sup>2–</sup> in high Si-Al slag, causing depolymerization of silica-alumina tetrahedra and forming berlinite. The AFTs of the mixed ash decreased to 1413 °C at 10 % P<sub>2</sub>O<sub>5</sub>. In high Ca-Fe slag, P formed the [PO<sub>4</sub>]<sup>3-</sup> tetrahedral structure and induced the repolymerization. The formation of calcium phosphate and anorthite increased the AFTs of the mixed ashes from 1206 °C to 1315 °C at 15 % P<sub>2</sub>O<sub>5</sub>.</div></div>","PeriodicalId":271,"journal":{"name":"Chemical Engineering Science","volume":"313 ","pages":"Article 121738"},"PeriodicalIF":4.1000,"publicationDate":"2025-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phosphorus-induced polymerization-depolymerization mechanism of high silica-alumina and high calcium-iron coal gasification slag network structure\",\"authors\":\"Chaoyue Zhao , Wei Zhao , Yuan Ma , Yonghui Bai , Yuchen Li , Xudong Song , Jiaofei Wang , Peng Lv , Qinghua Guo , Guangsuo Yu , Min Yao\",\"doi\":\"10.1016/j.ces.2025.121738\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The flow behavior of slag during the co-gasification of phosphorus-containing wastes and coal is crucial for developing the co-treatment technology of phosphorus-containing wastes in the entrained flow gasification. In this work, high silica-alumina (Si-Al) and high calcium-iron (Ca-Fe) coal were used as reference materials, simplified to SiO<sub>2</sub>-Al<sub>2</sub>O<sub>3</sub>-CaO-Fe<sub>2</sub>O<sub>3</sub>. Synthetic ash was prepared with oxidizing reagents, and P<sub>2</sub>O<sub>5</sub> was added to study its impact on coal ash flow behavior and the phosphorus-induced polymerization-depolymerization mechanisms in the slag network structure. Results showed that P<sup>5+</sup> competed with Si<sup>4+</sup> for Al<sup>3+</sup> and O<sup>2–</sup> in high Si-Al slag, causing depolymerization of silica-alumina tetrahedra and forming berlinite. The AFTs of the mixed ash decreased to 1413 °C at 10 % P<sub>2</sub>O<sub>5</sub>. In high Ca-Fe slag, P formed the [PO<sub>4</sub>]<sup>3-</sup> tetrahedral structure and induced the repolymerization. The formation of calcium phosphate and anorthite increased the AFTs of the mixed ashes from 1206 °C to 1315 °C at 15 % P<sub>2</sub>O<sub>5</sub>.</div></div>\",\"PeriodicalId\":271,\"journal\":{\"name\":\"Chemical Engineering Science\",\"volume\":\"313 \",\"pages\":\"Article 121738\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-04-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Engineering Science\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0009250925005615\",\"RegionNum\":2,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENGINEERING, CHEMICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Engineering Science","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0009250925005615","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
Phosphorus-induced polymerization-depolymerization mechanism of high silica-alumina and high calcium-iron coal gasification slag network structure
The flow behavior of slag during the co-gasification of phosphorus-containing wastes and coal is crucial for developing the co-treatment technology of phosphorus-containing wastes in the entrained flow gasification. In this work, high silica-alumina (Si-Al) and high calcium-iron (Ca-Fe) coal were used as reference materials, simplified to SiO2-Al2O3-CaO-Fe2O3. Synthetic ash was prepared with oxidizing reagents, and P2O5 was added to study its impact on coal ash flow behavior and the phosphorus-induced polymerization-depolymerization mechanisms in the slag network structure. Results showed that P5+ competed with Si4+ for Al3+ and O2– in high Si-Al slag, causing depolymerization of silica-alumina tetrahedra and forming berlinite. The AFTs of the mixed ash decreased to 1413 °C at 10 % P2O5. In high Ca-Fe slag, P formed the [PO4]3- tetrahedral structure and induced the repolymerization. The formation of calcium phosphate and anorthite increased the AFTs of the mixed ashes from 1206 °C to 1315 °C at 15 % P2O5.
期刊介绍:
Chemical engineering enables the transformation of natural resources and energy into useful products for society. It draws on and applies natural sciences, mathematics and economics, and has developed fundamental engineering science that underpins the discipline.
Chemical Engineering Science (CES) has been publishing papers on the fundamentals of chemical engineering since 1951. CES is the platform where the most significant advances in the discipline have ever since been published. Chemical Engineering Science has accompanied and sustained chemical engineering through its development into the vibrant and broad scientific discipline it is today.