The Gibbs energy of formation of huntite, CaMg 3 (CO 3 ) 4 , at 295 K and 1 bar from electrochemical cell measurements
Abstract
Other| April 01, 1995 The Gibbs energy of formation of huntite, CaMg3(CO3)4, at 295 K and 1 bar from electrochemical cell measurements Erin M. Walling; Erin M. Walling University of California, School of Medicine, Irvine, CA, United States Search for other works by this author on: GSW Google Scholar Peter A. Rock; Peter A. Rock Search for other works by this author on: GSW Google Scholar William H. Casey William H. Casey Search for other works by this author on: GSW Google Scholar Author and Article Information Erin M. Walling University of California, School of Medicine, Irvine, CA, United States Peter A. Rock William H. Casey Publisher: Mineralogical Society of America First Online: 02 Mar 2017 Online ISSN: 1945-3027 Print ISSN: 0003-004X Copyright © 1995 by the Mineralogical Society of America American Mineralogist (1995) 80 (3-4): 355–360. https://doi.org/10.2138/am-1995-3-417 Article history First Online: 02 Mar 2017 Cite View This Citation Add to Citation Manager Share Icon Share Facebook Twitter LinkedIn Email Permissions Search Site Citation Erin M. Walling, Peter A. Rock, William H. Casey; The Gibbs energy of formation of huntite, CaMg3(CO3)4, at 295 K and 1 bar from electrochemical cell measurements. American Mineralogist 1995;; 80 (3-4): 355–360. doi: https://doi.org/10.2138/am-1995-3-417 Download citation file: Ris (Zotero) Refmanager EasyBib Bookends Mendeley Papers EndNote RefWorks BibTex toolbar search Search Dropdown Menu toolbar search search input Search input auto suggest filter your search All ContentBy SocietyAmerican Mineralogist Search Advanced Search Abstract New data are presented for the ΔGf0 for huntite, CaMg3(CO3)4. Measurements were made using new third-kind electrochemical cells that do not require a complicated model for solute speciation or corrections for liquid-liquid junction potentials. The average value of ΔGf0[CaMg3(CO3)4(S)](−4195.6±6.4 kJ/mol) measured in these electrochemical cells agrees, within experimental error, with values determined calorimetricaUy (e.g., −4203.4 ± 1.6 kj/mol: Hemingway and Robie, 1973) and electrochemically (−4188.6 ± 1.0 kj/mol: Gamsjäger, 1989). Our results demonstrate the utility of this new electrochemical method in the study of metal carbonate equilibria of geochemical importance. This content is PDF only. Please click on the PDF icon to access. First Page Preview Close Modal You do not have access to this content, please speak to your institutional administrator if you feel you should have access.
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Hydromagnesite then very slowly transitions to magnesite until reaching 100 bar, the most favorable pressure for magnesite production.
“Hydromagnesite then very slowly transitions to magnesite until reaching 100 bar, the most favorable pressure for magnesite production.66”
From Utilization of mineral carbonation products: current state and potential (2019) · cites this paper as [66]
An investigation of Mg-carbonate systems found that the first species formed is metastable nesquehonite (25°C, 1 bar PCO2), followed by metastable hydromagnesite (120°C, 3 bar).
“An investigation of Mg-carbonate systems found that the first species formed is metastable nesquehonite (25°C, 1 bar P CO 2 ), followed by metastable hydromagnesite (120°C, 3 bar).”
From Utilization of mineral carbonation products: current state and potential (2019) · cites this paper as [66]
A low ratio of Mg2+ to CO3 2- could overcome the increased hydration activity of Mg2+ ions, allowing for easier adsorption on the crystal surface.
“A low ratio of Mg 2+ to CO 3 2-could overcome the increased hydration activity of Mg 2+ ions, as carbonate anions have a larger radius and are not completely surrounded by water.This allows for easier adsorption on the crystal surface.66”
From Utilization of mineral carbonation products: current state and potential (2019) · cites this paper as [66]
Cites
Stability of some carbonates at 25 degrees C and one atmosphere total pressure
Garrels, R. M., Thompson, M. E., & Siever, R. (1960) · American Journal of Science · doi:10.2475/ajs.258.6.402 · Cited by 297 · see citing works
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Low-temperature thermodynamic model for the system Na2CO3–MgCO3–CaCO3–H2O
Königsberger, E., Königsberger, L.-C., & Gamsjäger, H. (1999) · Geochimica et Cosmochimica Acta · doi:10.1016/s0016-7037(99)00238-0 · Cited by 275 · see citing works
Utilization of mineral carbonation products: current state and potential
Woodall, C. M., McQueen, N., Pilorgé, H., & Wilcox, J. (2019) · Greenhouse Gases Science and Technology · doi:10.1002/ghg.1940 · Cited by 149 · see citing works
- Authors
- Walling, E. M., Rock, P. A., & Casey, W. H.
- Affiliations
- University of California, Irvine (US)
- ORCID
- Casey, William H.
- Venue
- American Mineralogist
- Publisher
- Mineralogical Society of America
- Published
- 1995-04-01
- Volume
- 80
- Issue
- 3-4
- Pages
- 355-360
- ISSN
- 0003-004X (ISSN-L)
- OpenAlex
- W2183596460
- Cited by
- 6
- References
- 1
- Citations by year
- 2023: 1 · 2019: 1
- FWCI
- 0.30
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Mineralogist (publishedVersion)
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Chemical Thermodynamics and Molecular Structure
- Physical Sciences › Earth and Planetary Sciences › Geophysics › Geological and Geochemical Analysis
- Physical Sciences › Earth and Planetary Sciences › Geochemistry and Petrology › Mineralogy and Gemology Studies
- Keywords
- huntite, Gibbs energy of formation, calcium magnesium carbonate, carbonate minerals, electrochemical cells, thermodynamic properties, standard Gibbs energy of formation, standard enthalpy of formation, standard entropy, standard enthalpy of solution
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