M. Pollet-Villard , D. Daval , P. Ackerer , G.D. Saldi , K.G. Knauss , B. Wild , B. Fritz
{"title":"Experimental Study of Dissolution Kinetics of K-feldspar as a Function of Crystal Structure Anisotropy under Hydrothermal Conditions","authors":"M. Pollet-Villard , D. Daval , P. Ackerer , G.D. Saldi , K.G. Knauss , B. Wild , B. Fritz","doi":"10.1016/j.proeps.2016.12.042","DOIUrl":null,"url":null,"abstract":"<div><p>We present the results of an experimental study of the effect of anisotropy on the kinetics of K-Feldspar dissolution under hydrothermal conditions as encountered in the Soultz-sous-Forêts enhanced geothermal system. We try to quantify the impact of K-feldspar anisotropy on dissolution rates in order to develop a more comprehensive model of the evolution of the reactive surface of silicate minerals in order to propose alternate kinetic rate laws to be implemented into water-rock interaction models and reactive transport codes. Our results evidence a relation between K-spar dissolution rate and the Gibbs free energy of reaction (Δ<em>G</em><sub><em>r</em></sub>) which clearly differs from the transition state theory usually implemented into geochemical codes: it depends on the crystallographic orientation of K-spar mineral with significant differences between the different crystal faces. As for the far-from-equilibrium dissolution rate, this result highlights that using a unique theoretical rate law to describe dissolution rate as a function of Δ<em>G</em><sub><em>r</em></sub> remains highly questionable. These results are very important for our challenge of understanding and modelling the dissolution mechanisms and they evidence that the dissolution anisotropy plays a fundamental role in these mechanisms.</p></div>","PeriodicalId":101039,"journal":{"name":"Procedia Earth and Planetary Science","volume":"17 ","pages":"Pages 165-168"},"PeriodicalIF":0.0000,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.proeps.2016.12.042","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Procedia Earth and Planetary Science","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1878522016300741","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7
Abstract
We present the results of an experimental study of the effect of anisotropy on the kinetics of K-Feldspar dissolution under hydrothermal conditions as encountered in the Soultz-sous-Forêts enhanced geothermal system. We try to quantify the impact of K-feldspar anisotropy on dissolution rates in order to develop a more comprehensive model of the evolution of the reactive surface of silicate minerals in order to propose alternate kinetic rate laws to be implemented into water-rock interaction models and reactive transport codes. Our results evidence a relation between K-spar dissolution rate and the Gibbs free energy of reaction (ΔGr) which clearly differs from the transition state theory usually implemented into geochemical codes: it depends on the crystallographic orientation of K-spar mineral with significant differences between the different crystal faces. As for the far-from-equilibrium dissolution rate, this result highlights that using a unique theoretical rate law to describe dissolution rate as a function of ΔGr remains highly questionable. These results are very important for our challenge of understanding and modelling the dissolution mechanisms and they evidence that the dissolution anisotropy plays a fundamental role in these mechanisms.