{"title":"溶解氧在锌浸渣角石硫化—黄药浮选中的双重作用","authors":"Qing Shi , Feng Zhang , Chao Qi , Yan Miao","doi":"10.1016/j.seppur.2025.133232","DOIUrl":null,"url":null,"abstract":"<div><div>The recovery of valuable anglesite (PbSO<sub>4</sub>) from zinc leaching residue (ZLR) via sulfidation-xanthate flotation is hindered by poorly understood dissolved oxygen (DO) effects. This study clarifies the dual role of DO across sulfidation and xanthate adsorption stages. Micro-flotation experiments revealed that minimizing DO during the sulfidation stage reduced Na<sub>2</sub>S dosage, while optimal anglesite recovery required controlled DO levels (5.0–6.0 ppm) during xanthate conditioning stage. For sulfidation stage, zeta potential and XPS analysis revealed gradual surface oxidation with increasing DO, though PbS species remained relatively stable (0.2–6.0 ppm DO). For PAX conditioning stage, adsorption quantity, QCM-D and FTIR measurements revealed that 6.0 ppm DO enhanced xanthate adsorption on sulfurized anglesite. Bench-scale tests with nitrogen-regulated DO (1.8–4.2 ppm in sulfidation; 4.2–6.0 ppm in PAX conditioning) achieved higher Pb grade (23.3 % vs. 19.4 %) with comparable Pb recovery (60.9 % vs. 60.6 %), alongside a 26.7 % reduction in Na<sub>2</sub>S dosage (14,600 to 10,700 g/t). These findings establish DO as a pivotal operational parameter for balancing surface oxidation and xanthate adsorption, offering a reagent-saving strategy for anglesite recovery from ZLR.</div></div>","PeriodicalId":427,"journal":{"name":"Separation and Purification Technology","volume":"370 ","pages":"Article 133232"},"PeriodicalIF":9.0000,"publicationDate":"2025-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dual role of dissolved oxygen in sulfidation-xanthate flotation of anglesite from zinc leaching residue\",\"authors\":\"Qing Shi , Feng Zhang , Chao Qi , Yan Miao\",\"doi\":\"10.1016/j.seppur.2025.133232\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The recovery of valuable anglesite (PbSO<sub>4</sub>) from zinc leaching residue (ZLR) via sulfidation-xanthate flotation is hindered by poorly understood dissolved oxygen (DO) effects. This study clarifies the dual role of DO across sulfidation and xanthate adsorption stages. Micro-flotation experiments revealed that minimizing DO during the sulfidation stage reduced Na<sub>2</sub>S dosage, while optimal anglesite recovery required controlled DO levels (5.0–6.0 ppm) during xanthate conditioning stage. For sulfidation stage, zeta potential and XPS analysis revealed gradual surface oxidation with increasing DO, though PbS species remained relatively stable (0.2–6.0 ppm DO). For PAX conditioning stage, adsorption quantity, QCM-D and FTIR measurements revealed that 6.0 ppm DO enhanced xanthate adsorption on sulfurized anglesite. Bench-scale tests with nitrogen-regulated DO (1.8–4.2 ppm in sulfidation; 4.2–6.0 ppm in PAX conditioning) achieved higher Pb grade (23.3 % vs. 19.4 %) with comparable Pb recovery (60.9 % vs. 60.6 %), alongside a 26.7 % reduction in Na<sub>2</sub>S dosage (14,600 to 10,700 g/t). These findings establish DO as a pivotal operational parameter for balancing surface oxidation and xanthate adsorption, offering a reagent-saving strategy for anglesite recovery from ZLR.</div></div>\",\"PeriodicalId\":427,\"journal\":{\"name\":\"Separation and Purification Technology\",\"volume\":\"370 \",\"pages\":\"Article 133232\"},\"PeriodicalIF\":9.0000,\"publicationDate\":\"2025-04-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Separation and Purification Technology\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1383586625018295\",\"RegionNum\":1,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, CHEMICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Separation and Purification Technology","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1383586625018295","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
Dual role of dissolved oxygen in sulfidation-xanthate flotation of anglesite from zinc leaching residue
The recovery of valuable anglesite (PbSO4) from zinc leaching residue (ZLR) via sulfidation-xanthate flotation is hindered by poorly understood dissolved oxygen (DO) effects. This study clarifies the dual role of DO across sulfidation and xanthate adsorption stages. Micro-flotation experiments revealed that minimizing DO during the sulfidation stage reduced Na2S dosage, while optimal anglesite recovery required controlled DO levels (5.0–6.0 ppm) during xanthate conditioning stage. For sulfidation stage, zeta potential and XPS analysis revealed gradual surface oxidation with increasing DO, though PbS species remained relatively stable (0.2–6.0 ppm DO). For PAX conditioning stage, adsorption quantity, QCM-D and FTIR measurements revealed that 6.0 ppm DO enhanced xanthate adsorption on sulfurized anglesite. Bench-scale tests with nitrogen-regulated DO (1.8–4.2 ppm in sulfidation; 4.2–6.0 ppm in PAX conditioning) achieved higher Pb grade (23.3 % vs. 19.4 %) with comparable Pb recovery (60.9 % vs. 60.6 %), alongside a 26.7 % reduction in Na2S dosage (14,600 to 10,700 g/t). These findings establish DO as a pivotal operational parameter for balancing surface oxidation and xanthate adsorption, offering a reagent-saving strategy for anglesite recovery from ZLR.
期刊介绍:
Separation and Purification Technology is a premier journal committed to sharing innovative methods for separation and purification in chemical and environmental engineering, encompassing both homogeneous solutions and heterogeneous mixtures. Our scope includes the separation and/or purification of liquids, vapors, and gases, as well as carbon capture and separation techniques. However, it's important to note that methods solely intended for analytical purposes are not within the scope of the journal. Additionally, disciplines such as soil science, polymer science, and metallurgy fall outside the purview of Separation and Purification Technology. Join us in advancing the field of separation and purification methods for sustainable solutions in chemical and environmental engineering.