Enhanced leachability of rare earth elements from calcined products of bituminous coals

Wencai Zhang; Rick Honaker

doi:10.1016/j.mineng.2019.105935

Enhanced leachability of rare earth elements from calcined products of bituminous coals

Wencai Zhang, Rick Honaker

Research output: Contribution to journal › Article › peer-review

34 Scopus citations

Abstract

The modes of occurrence associated with rare earth elements (REEs) in bituminous coal sources were evaluated along with their potential recovery by calcination treatment at 600 ℃ followed by sequential extraction. The coal samples were collected from three different resources, i.e., Fire Clay, West Kentucky No. 13, and Illinois No. 6 seams. Sequential extraction tests indicated that the majority of REEs in the calcined samples occurred as metal oxides especially for the West Kentucky No. 13 calcined material (54% of total REEs), which is distinct from untreated coal and combustion byproducts from pulverized coal boilers reported in literature. In addition, heavy REEs were more likely associated with easily dissolvable forms (i.e., ion-exchangeable, carbonates, and metal oxides). The calcined samples were leached under weak acidic conditions with and without adding ammonium sulfate to recover REEs. About 13%, 24%, and 20% of the REEs were extracted from the Fire Clay, West Kentucky No. 13, and Illinois No. 6 materials, respectively, by leaching at pH 4.0. The addition of 1 M ammonium sulfate further increased the recovery values to 18%, 45%, and 32%, respectively. In addition, about 64% of HREEs were extracted from the West Kentucky No. 13 calcined material under this condition. As such, a significant portion of the REEs can be easily extracted from the samples obtained by calcining the coals at 600 ℃.

Original language	English
Article number	105935
Journal	Minerals Engineering
Volume	142
DOIs	https://doi.org/10.1016/j.mineng.2019.105935
State	Published - Oct 2019

Bibliographical note

Publisher Copyright:
© 2019 Elsevier Ltd

Funding

This material is based upon work supported by the Department of Energy under Award Number DE-FE0029900. Disclaimer: This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government nor any agency thereof, nor any of their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference herein to any specific commercial product, process, or service by trade name, trademark, manufacturer, or otherwise does not necessarily constitute or imply its endorsement, recommendation, or favoring by the United States Government or any agency thereof. The views and opinions of authors expressed herein do not necessarily state or reflect those of the United States Government or any agency thereof. This material is based upon work supported by the Department of Energy under Award Number DE-FE0029900 . Disclaimer: This report was prepared as an account of work sponsored by an agency of the United States Government . Neither the United States Government nor any agency thereof, nor any of their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference herein to any specific commercial product, process, or service by trade name, trademark, manufacturer, or otherwise does not necessarily constitute or imply its endorsement, recommendation, or favoring by the United States Government or any agency thereof. The views and opinions of authors expressed herein do not necessarily state or reflect those of the United States Government or any agency thereof.

Funders	Funder number
United States Government
U.S. Department of Energy EPSCoR	DE-FE0029900
U.S. Department of Energy EPSCoR

Keywords

Calcination
Coal
Mode of occurrence
Rare earth elements
Sequential extraction

ASJC Scopus subject areas

Control and Systems Engineering
General Chemistry
Geotechnical Engineering and Engineering Geology
Mechanical Engineering

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10.1016/j.mineng.2019.105935

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abstract = "The modes of occurrence associated with rare earth elements (REEs) in bituminous coal sources were evaluated along with their potential recovery by calcination treatment at 600 ℃ followed by sequential extraction. The coal samples were collected from three different resources, i.e., Fire Clay, West Kentucky No. 13, and Illinois No. 6 seams. Sequential extraction tests indicated that the majority of REEs in the calcined samples occurred as metal oxides especially for the West Kentucky No. 13 calcined material (54% of total REEs), which is distinct from untreated coal and combustion byproducts from pulverized coal boilers reported in literature. In addition, heavy REEs were more likely associated with easily dissolvable forms (i.e., ion-exchangeable, carbonates, and metal oxides). The calcined samples were leached under weak acidic conditions with and without adding ammonium sulfate to recover REEs. About 13%, 24%, and 20% of the REEs were extracted from the Fire Clay, West Kentucky No. 13, and Illinois No. 6 materials, respectively, by leaching at pH 4.0. The addition of 1 M ammonium sulfate further increased the recovery values to 18%, 45%, and 32%, respectively. In addition, about 64% of HREEs were extracted from the West Kentucky No. 13 calcined material under this condition. As such, a significant portion of the REEs can be easily extracted from the samples obtained by calcining the coals at 600 ℃.",

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AB - The modes of occurrence associated with rare earth elements (REEs) in bituminous coal sources were evaluated along with their potential recovery by calcination treatment at 600 ℃ followed by sequential extraction. The coal samples were collected from three different resources, i.e., Fire Clay, West Kentucky No. 13, and Illinois No. 6 seams. Sequential extraction tests indicated that the majority of REEs in the calcined samples occurred as metal oxides especially for the West Kentucky No. 13 calcined material (54% of total REEs), which is distinct from untreated coal and combustion byproducts from pulverized coal boilers reported in literature. In addition, heavy REEs were more likely associated with easily dissolvable forms (i.e., ion-exchangeable, carbonates, and metal oxides). The calcined samples were leached under weak acidic conditions with and without adding ammonium sulfate to recover REEs. About 13%, 24%, and 20% of the REEs were extracted from the Fire Clay, West Kentucky No. 13, and Illinois No. 6 materials, respectively, by leaching at pH 4.0. The addition of 1 M ammonium sulfate further increased the recovery values to 18%, 45%, and 32%, respectively. In addition, about 64% of HREEs were extracted from the West Kentucky No. 13 calcined material under this condition. As such, a significant portion of the REEs can be easily extracted from the samples obtained by calcining the coals at 600 ℃.

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Enhanced leachability of rare earth elements from calcined products of bituminous coals

Abstract

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Keywords

ASJC Scopus subject areas

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