John Demol , Elizabeth Ho , Karin Soldenhoff , Gamini Senanayake
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Hydroxyapatite addition significantly decreased the dissolution of rare earth elements from monazite in the leach after baking at temperatures above 300 °C. For a bake temperature of 500 °C, the rare earth dissolution in the leach dropped from 80% for monazite alone, to 30% for a 1:1 (<em>w</em>/<em>w</em>) addition of hydroxyapatite. This decrease in rare earth leaching was attributed to the formation of an insoluble thorium and rare earth bearing polyphosphate. The rare earth elements were incorporated into this polyphosphate phase in preference to calcium. At 800 °C, monazite was re-formed, causing a further reduction in rare earth extraction, while simultaneous formation of calcium pyrophosphate (Ca<sub>2</sub>P<sub>2</sub>O<sub>7</sub>) led to an increase in calcium and phosphorus dissolution. The detrimental effect of apatite could be partially overcome by the addition of goethite. Addition of goethite to the acid bake of a monazite/apatite mixture at 500 °C improved the total rare earth dissolution from 29% to 85% in the subsequent leach. Results also demonstrated that the order of reactivity, in terms of formation of polyphosphates is Fe > REE > Ca.</p></div>","PeriodicalId":13193,"journal":{"name":"Hydrometallurgy","volume":"226 ","pages":"Article 106296"},"PeriodicalIF":4.8000,"publicationDate":"2024-03-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The impact of apatite on sulfuric acid baking of a monazite concentrate and the benefit of goethite addition on rare earth leaching\",\"authors\":\"John Demol , Elizabeth Ho , Karin Soldenhoff , Gamini Senanayake\",\"doi\":\"10.1016/j.hydromet.2024.106296\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Sulfuric acid baking of monazite ((Ce,La,Th)PO<sub>4</sub>) bearing ores is one of the major processes used in commercial production of rare earth elements. In hydrothermal vein type rare earth deposits, apatite is often found together with monazite. Rare earth enriched fluorapatite ores may also contain significant amounts of rare earths hosted in monazite. An understanding of the effect of apatite on the sulfuric acid baking of monazite is therefore important for the development of effective sulfuric acid based treatment methods for such ores. In this work, the addition of a natural hydroxyapatite (Ca<sub>5</sub>(PO<sub>4</sub>)<sub>3</sub>(OH)) sample to a monazite acid bake followed by acid leach was investigated using a combination of chemical analyses, SEM-EDS, XRD and TG-DSC. Hydroxyapatite addition significantly decreased the dissolution of rare earth elements from monazite in the leach after baking at temperatures above 300 °C. For a bake temperature of 500 °C, the rare earth dissolution in the leach dropped from 80% for monazite alone, to 30% for a 1:1 (<em>w</em>/<em>w</em>) addition of hydroxyapatite. This decrease in rare earth leaching was attributed to the formation of an insoluble thorium and rare earth bearing polyphosphate. The rare earth elements were incorporated into this polyphosphate phase in preference to calcium. At 800 °C, monazite was re-formed, causing a further reduction in rare earth extraction, while simultaneous formation of calcium pyrophosphate (Ca<sub>2</sub>P<sub>2</sub>O<sub>7</sub>) led to an increase in calcium and phosphorus dissolution. The detrimental effect of apatite could be partially overcome by the addition of goethite. Addition of goethite to the acid bake of a monazite/apatite mixture at 500 °C improved the total rare earth dissolution from 29% to 85% in the subsequent leach. Results also demonstrated that the order of reactivity, in terms of formation of polyphosphates is Fe > REE > Ca.</p></div>\",\"PeriodicalId\":13193,\"journal\":{\"name\":\"Hydrometallurgy\",\"volume\":\"226 \",\"pages\":\"Article 106296\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2024-03-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Hydrometallurgy\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0304386X24000367\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"METALLURGY & METALLURGICAL ENGINEERING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hydrometallurgy","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0304386X24000367","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"METALLURGY & METALLURGICAL ENGINEERING","Score":null,"Total":0}
引用次数: 0
摘要
含独居石((Ce,La,Th)PO)矿石的硫酸焙烧是稀土元素商业化生产的主要工艺之一。在热液矿脉型稀土矿床中,磷灰石通常与独居石一起存在。富含稀土的氟磷灰石矿石也可能含有大量寄生在独居石中的稀土。因此,了解磷灰石对硫酸焙烧独居石的影响对于开发基于硫酸的有效处理此类矿石的方法非常重要。在这项工作中,采用化学分析、SEM-EDS、XRD 和 TG-DSC 等综合方法,研究了在独居石酸焙烧中添加天然羟基磷灰石(Ca(PO)(OH))样品,然后进行酸浸出的问题。在 300 °C 以上的烘焙温度下,添加羟基磷灰石可显著减少浸出液中稀土元素从独居石中的溶出。烘焙温度为 500 ℃ 时,浸出液中稀土的溶解度从单独使用独居石时的 80% 降至添加 1:1 (/) 羟基磷灰石时的 30%。稀土浸出率下降的原因是形成了一种不溶于水的含钍和稀土的多磷酸盐。稀土元素优先于钙元素被掺入这种多磷酸盐相中。在 800 °C 时,独居石重新形成,导致稀土萃取进一步减少,同时焦磷酸钙(CaPO)的形成导致钙和磷的溶解增加。磷灰石的不利影响可以通过添加鹅辉石得到部分克服。在 500 °C 下对独居石/磷灰石混合物进行酸焙烧时,加入高铁铝土可将随后浸出过程中的稀土总溶解度从 29% 提高到 85%。结果还表明,就多磷酸盐的形成而言,反应性顺序为铁 > 稀土 > 钙。
The impact of apatite on sulfuric acid baking of a monazite concentrate and the benefit of goethite addition on rare earth leaching
Sulfuric acid baking of monazite ((Ce,La,Th)PO4) bearing ores is one of the major processes used in commercial production of rare earth elements. In hydrothermal vein type rare earth deposits, apatite is often found together with monazite. Rare earth enriched fluorapatite ores may also contain significant amounts of rare earths hosted in monazite. An understanding of the effect of apatite on the sulfuric acid baking of monazite is therefore important for the development of effective sulfuric acid based treatment methods for such ores. In this work, the addition of a natural hydroxyapatite (Ca5(PO4)3(OH)) sample to a monazite acid bake followed by acid leach was investigated using a combination of chemical analyses, SEM-EDS, XRD and TG-DSC. Hydroxyapatite addition significantly decreased the dissolution of rare earth elements from monazite in the leach after baking at temperatures above 300 °C. For a bake temperature of 500 °C, the rare earth dissolution in the leach dropped from 80% for monazite alone, to 30% for a 1:1 (w/w) addition of hydroxyapatite. This decrease in rare earth leaching was attributed to the formation of an insoluble thorium and rare earth bearing polyphosphate. The rare earth elements were incorporated into this polyphosphate phase in preference to calcium. At 800 °C, monazite was re-formed, causing a further reduction in rare earth extraction, while simultaneous formation of calcium pyrophosphate (Ca2P2O7) led to an increase in calcium and phosphorus dissolution. The detrimental effect of apatite could be partially overcome by the addition of goethite. Addition of goethite to the acid bake of a monazite/apatite mixture at 500 °C improved the total rare earth dissolution from 29% to 85% in the subsequent leach. Results also demonstrated that the order of reactivity, in terms of formation of polyphosphates is Fe > REE > Ca.
期刊介绍:
Hydrometallurgy aims to compile studies on novel processes, process design, chemistry, modelling, control, economics and interfaces between unit operations, and to provide a forum for discussions on case histories and operational difficulties.
Topics covered include: leaching of metal values by chemical reagents or bacterial action at ambient or elevated pressures and temperatures; separation of solids from leach liquors; removal of impurities and recovery of metal values by precipitation, ion exchange, solvent extraction, gaseous reduction, cementation, electro-winning and electro-refining; pre-treatment of ores by roasting or chemical treatments such as halogenation or reduction; recycling of reagents and treatment of effluents.