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Dynamic pore structure evolution of the ion adsorbed rare earth ore during the ion exchange process

During the leaching process of the ion-adsorbed rare earth (RE) ore, the pore structure evolution of the ore body plays a vital role in the seepage of the leaching solution. To investigate the evolution of the pore structure during the leaching process, experiments have been carried out with remodel...

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Autores principales: Zhou, Lingbo, Wang, Xiaojun, Zhuo, Yulong, Hu, Kaijian, Zhong, Wen, Huang, Guangli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894599/
https://www.ncbi.nlm.nih.gov/pubmed/31827847
http://dx.doi.org/10.1098/rsos.191107
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author Zhou, Lingbo
Wang, Xiaojun
Zhuo, Yulong
Hu, Kaijian
Zhong, Wen
Huang, Guangli
author_facet Zhou, Lingbo
Wang, Xiaojun
Zhuo, Yulong
Hu, Kaijian
Zhong, Wen
Huang, Guangli
author_sort Zhou, Lingbo
collection PubMed
description During the leaching process of the ion-adsorbed rare earth (RE) ore, the pore structure evolution of the ore body plays a vital role in the seepage of the leaching solution. To investigate the evolution of the pore structure during the leaching process, experiments have been carried out with remodelled RE ore samples based on the physical characteristics of in situ ores. The seepage rate difference between deionized water leaching solution and 2% NH(4)Cl leaching solution during the active leaching period was analysed. The porosity and the dynamic pore size evolution of pore structures in the ore body are discussed. Results indicate that along with ion exchange between the RE ore and the leaching solution, the porosity of the sample remains constant and the pore structure shows a decreasing trend in the first part and an increasing trend in the second part. Specifically, during the ion exchange process, the number of minimal pores (0–5 µm), small pores (5–10 µm) and medium pores (10–25 µm) increases significantly and the number of medium–large pores (25–60 µm), large pores (60–120 µm) and mega pores (greater than 120 µm) decreases dramatically. Along with the completion of the ion exchange process, the evolution of porous structure shows an opposite trend. The mechanism study reveals that the evolution of pore structure is induced by the difference of ionic strength in the leaching solution during the ion exchange process, where the RE ore microparticles will be absorbed or desorbed on to the solid phase.
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spelling pubmed-68945992019-12-11 Dynamic pore structure evolution of the ion adsorbed rare earth ore during the ion exchange process Zhou, Lingbo Wang, Xiaojun Zhuo, Yulong Hu, Kaijian Zhong, Wen Huang, Guangli R Soc Open Sci Chemistry During the leaching process of the ion-adsorbed rare earth (RE) ore, the pore structure evolution of the ore body plays a vital role in the seepage of the leaching solution. To investigate the evolution of the pore structure during the leaching process, experiments have been carried out with remodelled RE ore samples based on the physical characteristics of in situ ores. The seepage rate difference between deionized water leaching solution and 2% NH(4)Cl leaching solution during the active leaching period was analysed. The porosity and the dynamic pore size evolution of pore structures in the ore body are discussed. Results indicate that along with ion exchange between the RE ore and the leaching solution, the porosity of the sample remains constant and the pore structure shows a decreasing trend in the first part and an increasing trend in the second part. Specifically, during the ion exchange process, the number of minimal pores (0–5 µm), small pores (5–10 µm) and medium pores (10–25 µm) increases significantly and the number of medium–large pores (25–60 µm), large pores (60–120 µm) and mega pores (greater than 120 µm) decreases dramatically. Along with the completion of the ion exchange process, the evolution of porous structure shows an opposite trend. The mechanism study reveals that the evolution of pore structure is induced by the difference of ionic strength in the leaching solution during the ion exchange process, where the RE ore microparticles will be absorbed or desorbed on to the solid phase. The Royal Society 2019-11-06 /pmc/articles/PMC6894599/ /pubmed/31827847 http://dx.doi.org/10.1098/rsos.191107 Text en © 2019 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Chemistry
Zhou, Lingbo
Wang, Xiaojun
Zhuo, Yulong
Hu, Kaijian
Zhong, Wen
Huang, Guangli
Dynamic pore structure evolution of the ion adsorbed rare earth ore during the ion exchange process
title Dynamic pore structure evolution of the ion adsorbed rare earth ore during the ion exchange process
title_full Dynamic pore structure evolution of the ion adsorbed rare earth ore during the ion exchange process
title_fullStr Dynamic pore structure evolution of the ion adsorbed rare earth ore during the ion exchange process
title_full_unstemmed Dynamic pore structure evolution of the ion adsorbed rare earth ore during the ion exchange process
title_short Dynamic pore structure evolution of the ion adsorbed rare earth ore during the ion exchange process
title_sort dynamic pore structure evolution of the ion adsorbed rare earth ore during the ion exchange process
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894599/
https://www.ncbi.nlm.nih.gov/pubmed/31827847
http://dx.doi.org/10.1098/rsos.191107
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