LAPSE:2023.0956
Published Article

LAPSE:2023.0956
Precipitation of Ferrous Oxalate from Ferrous Ammonium Sulfate in Oxalic Acid Solution
February 21, 2023
Abstract
A kinetic study was conducted experimentally for the precipitation of ferrous oxalate. The ferrous oxalate, in the form of dihydrate (FeC2O4·2H2O), was produced by the acidic dissolution of ferrous ammonium sulfate (Fe(NH4)2(SO4)2) in an aqueous solution of oxalic acid, and then precipitated by nucleation and particle growth from supersaturated solution. The effect of the concentration of ferrous ammonium sulfate and oxalic acid as raw materials was investigated on the kinetics of the ferrous oxalate precipitation. Temperature was kept constant at 25 °C. The surface morphology, atomic compositions, and crystal phase were characterized for the ferrous oxalate precipitate collected. As the initial concentration of ferrous ammonium sulfate increased, the initial precipitation of ferrous oxalate occurred faster. The concentration of oxalic acid did not significantly affect the rate of precipitation of ferrous oxalate. The experimental behavior of ferrous oxalate precipitation was modeled with first-order models of reaction kinetics.
A kinetic study was conducted experimentally for the precipitation of ferrous oxalate. The ferrous oxalate, in the form of dihydrate (FeC2O4·2H2O), was produced by the acidic dissolution of ferrous ammonium sulfate (Fe(NH4)2(SO4)2) in an aqueous solution of oxalic acid, and then precipitated by nucleation and particle growth from supersaturated solution. The effect of the concentration of ferrous ammonium sulfate and oxalic acid as raw materials was investigated on the kinetics of the ferrous oxalate precipitation. Temperature was kept constant at 25 °C. The surface morphology, atomic compositions, and crystal phase were characterized for the ferrous oxalate precipitate collected. As the initial concentration of ferrous ammonium sulfate increased, the initial precipitation of ferrous oxalate occurred faster. The concentration of oxalic acid did not significantly affect the rate of precipitation of ferrous oxalate. The experimental behavior of ferrous oxalate precipitation was modeled with first-order models of reaction kinetics.
Record ID
Keywords
chemical decontamination, ferrous ammonium sulfate, ferrous oxalate, kinetics, oxalic acid, precipitation
Subject
Suggested Citation
Lee SI, Kim HR, Park JK, Oh W, Kim J, Kim C, Lee J, Kim KC, Lee BC. Precipitation of Ferrous Oxalate from Ferrous Ammonium Sulfate in Oxalic Acid Solution. (2023). LAPSE:2023.0956
Author Affiliations
Lee SI: Department of Chemical Engineering, Hannam University, Daejeon 34054, Republic of Korea
Kim HR: Department of Chemical Engineering, Hannam University, Daejeon 34054, Republic of Korea
Park JK: Department of Chemical Engineering, Hannam University, Daejeon 34054, Republic of Korea
Oh W: Research Institute of Advanced Energy Technology, Kyungpook National University, Daegu 41566, Republic of Korea
Kim J: KHNP Central Research Institute, Daejeon 34101, Republic of Korea [ORCID]
Kim C: KHNP Central Research Institute, Daejeon 34101, Republic of Korea
Lee J: KEPCO KPS, Busan 46036, Republic of Korea [ORCID]
Kim KC: KEPCO KPS, Busan 46036, Republic of Korea
Lee BC: Department of Chemical Engineering, Hannam University, Daejeon 34054, Republic of Korea
Kim HR: Department of Chemical Engineering, Hannam University, Daejeon 34054, Republic of Korea
Park JK: Department of Chemical Engineering, Hannam University, Daejeon 34054, Republic of Korea
Oh W: Research Institute of Advanced Energy Technology, Kyungpook National University, Daegu 41566, Republic of Korea
Kim J: KHNP Central Research Institute, Daejeon 34101, Republic of Korea [ORCID]
Kim C: KHNP Central Research Institute, Daejeon 34101, Republic of Korea
Lee J: KEPCO KPS, Busan 46036, Republic of Korea [ORCID]
Kim KC: KEPCO KPS, Busan 46036, Republic of Korea
Lee BC: Department of Chemical Engineering, Hannam University, Daejeon 34054, Republic of Korea
Journal Name
Processes
Volume
10
Issue
11
First Page
2420
Year
2022
Publication Date
2022-11-17
ISSN
2227-9717
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Original Submission
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PII: pr10112420, Publication Type: Journal Article
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LAPSE:2023.0956
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https://doi.org/10.3390/pr10112420
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Feb 21, 2023
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