W. Carlin, B. Malvoisin, F. Brunet, B. Lanson, N. Findling, M. Lanson, T. Fargetton, L. Jeannin, O. Lhote
{"title":"超基性岩中铁青金石氧化作用低温产生 H2 的动力学过程","authors":"W. Carlin, B. Malvoisin, F. Brunet, B. Lanson, N. Findling, M. Lanson, T. Fargetton, L. Jeannin, O. Lhote","doi":"10.7185/geochemlet.2408","DOIUrl":null,"url":null,"abstract":"Ferroan brucite, (Mg,Fe)(OH)<sub>2</sub>, is among the potential mineral candidates for low temperature (<423 K) abiotic H<sub>2</sub> production in ultramafic rocks. To verify this assumption, synthetic ferroan brucite with grain size similar to that observed in natural samples (40–100 nm) was reacted with pure water at temperatures ranging from 348 to 573 K. Experimental products are consistent with the reaction 3 Fe(OH)<sub>2</sub><sup>brucite</sup> = Fe<sub>3</sub>O<sub>4</sub> + H<sub>2</sub> + 2 H<sub>2</sub>O. This reaction reached completion in ∼2 months at 378 K and is thermally activated with an activation energy of 145 ± 1 kJ/mol. The standard state formation enthalpy and the third law entropy of amakinite, Fe(OH)<sub>2</sub>, were refined from the experimental dataset. The new thermodynamic parameters imply that ferroan brucite is stable at significantly lower hydrogen activity than previously calculated. The alteration of Fe-brucite produces H<sub>2</sub> at rates compatible with present day observations of H<sub>2</sub> emissions in natural settings (ophiolite and mid-oceanic ridges). However, efficient fluid renewal is required, as opposed to H<sub>2</sub> production through olivine serpentinisation, which can proceed in static hydraulic conditions.","PeriodicalId":12613,"journal":{"name":"Geochemical Perspectives Letters","volume":"23 1","pages":""},"PeriodicalIF":3.4000,"publicationDate":"2024-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Kinetics of low-temperature H2 production in ultramafic rocks by ferroan brucite oxidation\",\"authors\":\"W. Carlin, B. Malvoisin, F. Brunet, B. Lanson, N. Findling, M. Lanson, T. Fargetton, L. Jeannin, O. Lhote\",\"doi\":\"10.7185/geochemlet.2408\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Ferroan brucite, (Mg,Fe)(OH)<sub>2</sub>, is among the potential mineral candidates for low temperature (<423 K) abiotic H<sub>2</sub> production in ultramafic rocks. To verify this assumption, synthetic ferroan brucite with grain size similar to that observed in natural samples (40–100 nm) was reacted with pure water at temperatures ranging from 348 to 573 K. Experimental products are consistent with the reaction 3 Fe(OH)<sub>2</sub><sup>brucite</sup> = Fe<sub>3</sub>O<sub>4</sub> + H<sub>2</sub> + 2 H<sub>2</sub>O. This reaction reached completion in ∼2 months at 378 K and is thermally activated with an activation energy of 145 ± 1 kJ/mol. The standard state formation enthalpy and the third law entropy of amakinite, Fe(OH)<sub>2</sub>, were refined from the experimental dataset. The new thermodynamic parameters imply that ferroan brucite is stable at significantly lower hydrogen activity than previously calculated. The alteration of Fe-brucite produces H<sub>2</sub> at rates compatible with present day observations of H<sub>2</sub> emissions in natural settings (ophiolite and mid-oceanic ridges). However, efficient fluid renewal is required, as opposed to H<sub>2</sub> production through olivine serpentinisation, which can proceed in static hydraulic conditions.\",\"PeriodicalId\":12613,\"journal\":{\"name\":\"Geochemical Perspectives Letters\",\"volume\":\"23 1\",\"pages\":\"\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2024-03-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Geochemical Perspectives Letters\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://doi.org/10.7185/geochemlet.2408\",\"RegionNum\":1,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"GEOCHEMISTRY & GEOPHYSICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Geochemical Perspectives Letters","FirstCategoryId":"89","ListUrlMain":"https://doi.org/10.7185/geochemlet.2408","RegionNum":1,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GEOCHEMISTRY & GEOPHYSICS","Score":null,"Total":0}
Kinetics of low-temperature H2 production in ultramafic rocks by ferroan brucite oxidation
Ferroan brucite, (Mg,Fe)(OH)2, is among the potential mineral candidates for low temperature (<423 K) abiotic H2 production in ultramafic rocks. To verify this assumption, synthetic ferroan brucite with grain size similar to that observed in natural samples (40–100 nm) was reacted with pure water at temperatures ranging from 348 to 573 K. Experimental products are consistent with the reaction 3 Fe(OH)2brucite = Fe3O4 + H2 + 2 H2O. This reaction reached completion in ∼2 months at 378 K and is thermally activated with an activation energy of 145 ± 1 kJ/mol. The standard state formation enthalpy and the third law entropy of amakinite, Fe(OH)2, were refined from the experimental dataset. The new thermodynamic parameters imply that ferroan brucite is stable at significantly lower hydrogen activity than previously calculated. The alteration of Fe-brucite produces H2 at rates compatible with present day observations of H2 emissions in natural settings (ophiolite and mid-oceanic ridges). However, efficient fluid renewal is required, as opposed to H2 production through olivine serpentinisation, which can proceed in static hydraulic conditions.
期刊介绍:
Geochemical Perspectives Letters is an open access, internationally peer-reviewed journal of the European Association of Geochemistry (EAG) that publishes short, highest-quality articles spanning geochemical sciences. The journal aims at rapid publication of the most novel research in geochemistry with a focus on outstanding quality, international importance, originality, and stimulating new developments across the vast array of geochemical disciplines.