Li Zeng, Tongjiang Peng, Hongjuan Sun, Xiyue Zhang, Dingran Zhao
{"title":"蒙脱石在不同 pH 值的草酸和硫酸介质中的溶解过程和机理","authors":"Li Zeng, Tongjiang Peng, Hongjuan Sun, Xiyue Zhang, Dingran Zhao","doi":"10.1016/j.clay.2024.107573","DOIUrl":null,"url":null,"abstract":"<div><p>The dissolution of silicate minerals plays a crucial role in many natural geological processes. In order to better comprehend the reaction mechanisms and dissolution characteristics of montmorillonite in different acidic systems, the effects of interfacial reactions of montmorillonite with oxalic and sulfuric acid solutions at various pH levels on the ionic dissolution, crystal structure, and micro-morphology were studied, and the morphology of aluminum and saturation index of secondary mineral were simulated. It was shown that the dissolution amounts of Mg<sup>2+</sup>, Al<sup>3+</sup> and Si<sup>4+</sup> in montmorillonite structure decreased with the increase of pH value, which reflected the dependence of montmorillonite dissolution on the pH value of solution. The dissolution percentages of Mg<sup>2+</sup>, Al<sup>3+</sup> and Si<sup>4+</sup> after the reaction of montmorillonite with oxalic acid solution were greater than those in sulfuric acid solution, and the highest dissolution rate of Al<sup>3+</sup>, indicated that both ligands and protons attacked the surface sites of montmorillonite and accelerated the dissolution of ions. Moreover, oxalate ligands exerted specific binding effects on Al<sup>3+</sup> ions. While reacting with oxalate and sulfate, the tetrahedral, octahedral and interlayer cations of montmorillonite exhibited the non-stoichiometric and inconsistent dissolution. The oxalate ligands have a strong complexation effect on Al<sup>3+</sup>, so that Al<sup>3+</sup> in oxalate solution exists in the form of aluminum oxalate complex, which reduces the effective concentration of Al<sup>3+</sup> in solution and promotes the dissolution of Al<sup>3+</sup> in montmorillonite structure. The Mg<sup>2+</sup> ions settled at octahedral substitution sites possessed weak stability, while those from the interlayer featured strong interlayer interchangeability, demonstrating the dissolution percentage up to 10.85 % and 8.62 % even in oxalic and sulfuric acid solutions at pH of 6.5. All secondary mineral phases in the solution were undersaturated, making the montmorillonite dissolution difficult to balance. Montmorillonite has a high cation exchange capacity, which makes it have a strong buffer capacity to exogenous acids. This study helps to explain the dissolution process of montmorillonite in inorganic and organic acid solutions at different pH value.</p></div>","PeriodicalId":245,"journal":{"name":"Applied Clay Science","volume":"261 ","pages":"Article 107573"},"PeriodicalIF":5.3000,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dissolution process and mechanism of montmorillonite in oxalic acid and sulfuric acid media at various pH levels\",\"authors\":\"Li Zeng, Tongjiang Peng, Hongjuan Sun, Xiyue Zhang, Dingran Zhao\",\"doi\":\"10.1016/j.clay.2024.107573\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The dissolution of silicate minerals plays a crucial role in many natural geological processes. In order to better comprehend the reaction mechanisms and dissolution characteristics of montmorillonite in different acidic systems, the effects of interfacial reactions of montmorillonite with oxalic and sulfuric acid solutions at various pH levels on the ionic dissolution, crystal structure, and micro-morphology were studied, and the morphology of aluminum and saturation index of secondary mineral were simulated. It was shown that the dissolution amounts of Mg<sup>2+</sup>, Al<sup>3+</sup> and Si<sup>4+</sup> in montmorillonite structure decreased with the increase of pH value, which reflected the dependence of montmorillonite dissolution on the pH value of solution. The dissolution percentages of Mg<sup>2+</sup>, Al<sup>3+</sup> and Si<sup>4+</sup> after the reaction of montmorillonite with oxalic acid solution were greater than those in sulfuric acid solution, and the highest dissolution rate of Al<sup>3+</sup>, indicated that both ligands and protons attacked the surface sites of montmorillonite and accelerated the dissolution of ions. Moreover, oxalate ligands exerted specific binding effects on Al<sup>3+</sup> ions. While reacting with oxalate and sulfate, the tetrahedral, octahedral and interlayer cations of montmorillonite exhibited the non-stoichiometric and inconsistent dissolution. The oxalate ligands have a strong complexation effect on Al<sup>3+</sup>, so that Al<sup>3+</sup> in oxalate solution exists in the form of aluminum oxalate complex, which reduces the effective concentration of Al<sup>3+</sup> in solution and promotes the dissolution of Al<sup>3+</sup> in montmorillonite structure. The Mg<sup>2+</sup> ions settled at octahedral substitution sites possessed weak stability, while those from the interlayer featured strong interlayer interchangeability, demonstrating the dissolution percentage up to 10.85 % and 8.62 % even in oxalic and sulfuric acid solutions at pH of 6.5. All secondary mineral phases in the solution were undersaturated, making the montmorillonite dissolution difficult to balance. Montmorillonite has a high cation exchange capacity, which makes it have a strong buffer capacity to exogenous acids. This study helps to explain the dissolution process of montmorillonite in inorganic and organic acid solutions at different pH value.</p></div>\",\"PeriodicalId\":245,\"journal\":{\"name\":\"Applied Clay Science\",\"volume\":\"261 \",\"pages\":\"Article 107573\"},\"PeriodicalIF\":5.3000,\"publicationDate\":\"2024-09-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied Clay Science\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0169131724003211\",\"RegionNum\":2,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Clay Science","FirstCategoryId":"89","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0169131724003211","RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Dissolution process and mechanism of montmorillonite in oxalic acid and sulfuric acid media at various pH levels
The dissolution of silicate minerals plays a crucial role in many natural geological processes. In order to better comprehend the reaction mechanisms and dissolution characteristics of montmorillonite in different acidic systems, the effects of interfacial reactions of montmorillonite with oxalic and sulfuric acid solutions at various pH levels on the ionic dissolution, crystal structure, and micro-morphology were studied, and the morphology of aluminum and saturation index of secondary mineral were simulated. It was shown that the dissolution amounts of Mg2+, Al3+ and Si4+ in montmorillonite structure decreased with the increase of pH value, which reflected the dependence of montmorillonite dissolution on the pH value of solution. The dissolution percentages of Mg2+, Al3+ and Si4+ after the reaction of montmorillonite with oxalic acid solution were greater than those in sulfuric acid solution, and the highest dissolution rate of Al3+, indicated that both ligands and protons attacked the surface sites of montmorillonite and accelerated the dissolution of ions. Moreover, oxalate ligands exerted specific binding effects on Al3+ ions. While reacting with oxalate and sulfate, the tetrahedral, octahedral and interlayer cations of montmorillonite exhibited the non-stoichiometric and inconsistent dissolution. The oxalate ligands have a strong complexation effect on Al3+, so that Al3+ in oxalate solution exists in the form of aluminum oxalate complex, which reduces the effective concentration of Al3+ in solution and promotes the dissolution of Al3+ in montmorillonite structure. The Mg2+ ions settled at octahedral substitution sites possessed weak stability, while those from the interlayer featured strong interlayer interchangeability, demonstrating the dissolution percentage up to 10.85 % and 8.62 % even in oxalic and sulfuric acid solutions at pH of 6.5. All secondary mineral phases in the solution were undersaturated, making the montmorillonite dissolution difficult to balance. Montmorillonite has a high cation exchange capacity, which makes it have a strong buffer capacity to exogenous acids. This study helps to explain the dissolution process of montmorillonite in inorganic and organic acid solutions at different pH value.
期刊介绍:
Applied Clay Science aims to be an international journal attracting high quality scientific papers on clays and clay minerals, including research papers, reviews, and technical notes. The journal covers typical subjects of Fundamental and Applied Clay Science such as:
• Synthesis and purification
• Structural, crystallographic and mineralogical properties of clays and clay minerals
• Thermal properties of clays and clay minerals
• Physico-chemical properties including i) surface and interface properties; ii) thermodynamic properties; iii) mechanical properties
• Interaction with water, with polar and apolar molecules
• Colloidal properties and rheology
• Adsorption, Intercalation, Ionic exchange
• Genesis and deposits of clay minerals
• Geology and geochemistry of clays
• Modification of clays and clay minerals properties by thermal and physical treatments
• Modification by chemical treatments with organic and inorganic molecules(organoclays, pillared clays)
• Modification by biological microorganisms. etc...