Carina Silke Hanser, Tobias Häger, Roman Botcharnikov
{"title":"Incorporation and substitution of ions and H2O in the structure of beryl","authors":"Carina Silke Hanser, Tobias Häger, Roman Botcharnikov","doi":"10.5194/ejm-36-449-2024","DOIUrl":null,"url":null,"abstract":"Abstract. Incorporation of ions into the crystal structure of beryl (Be3Al2[Si6O18]) can take place by direct ion-to-ion substitution of the framework components Al3+, Be2+ and Si4+ or by occupation of interstitial or structural channel sites. The most common impurities in beryl include transition metals, alkalis and H2O. It is accepted that the transition metals Mn, Cr and V directly substitute for Al at the octahedral site and induce colour. Similarly, the octahedral site can host Fe instead of Al. Nevertheless, it is shown that it remains disputed whether Fe can also be present at the tetrahedral, interstitial, or channel sites, and opposing hypotheses exist regarding these possibilities. However, in the case of Fe, not only the possible occupation of these sites remains under debate, but also their influence on the subsequent colour of beryl. Similarly, the residence of Li in the channels and at the Be tetrahedral or interstitial tetrahedral sites is still under debate. The presence of more than two types of H2O (type I and type II) in the structural channels of beryl is also unclear. This article aims to give an overview on the consensus and on the current debates found in the literature regarding these aspects. It mainly concentrates on the substitution by and the role of Fe ions and on channel occupancy by H2O.\n","PeriodicalId":11971,"journal":{"name":"European Journal of Mineralogy","volume":null,"pages":null},"PeriodicalIF":1.8000,"publicationDate":"2024-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Mineralogy","FirstCategoryId":"89","ListUrlMain":"https://doi.org/10.5194/ejm-36-449-2024","RegionNum":3,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MINERALOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Abstract. Incorporation of ions into the crystal structure of beryl (Be3Al2[Si6O18]) can take place by direct ion-to-ion substitution of the framework components Al3+, Be2+ and Si4+ or by occupation of interstitial or structural channel sites. The most common impurities in beryl include transition metals, alkalis and H2O. It is accepted that the transition metals Mn, Cr and V directly substitute for Al at the octahedral site and induce colour. Similarly, the octahedral site can host Fe instead of Al. Nevertheless, it is shown that it remains disputed whether Fe can also be present at the tetrahedral, interstitial, or channel sites, and opposing hypotheses exist regarding these possibilities. However, in the case of Fe, not only the possible occupation of these sites remains under debate, but also their influence on the subsequent colour of beryl. Similarly, the residence of Li in the channels and at the Be tetrahedral or interstitial tetrahedral sites is still under debate. The presence of more than two types of H2O (type I and type II) in the structural channels of beryl is also unclear. This article aims to give an overview on the consensus and on the current debates found in the literature regarding these aspects. It mainly concentrates on the substitution by and the role of Fe ions and on channel occupancy by H2O.
期刊介绍:
EJM was founded to reach a large audience on an international scale and also for achieving closer cooperation of European countries in the publication of scientific results. The founding societies have set themselves the task of publishing a journal of the highest standard open to all scientists performing mineralogical research in the widest sense of the term, all over the world. Contributions will therefore be published primarily in English.
EJM publishes original papers, review articles and letters dealing with the mineralogical sciences s.l., primarily mineralogy, petrology, geochemistry, crystallography and ore deposits, but also biomineralogy, environmental, applied and technical mineralogy. Nevertheless, papers in any related field, including cultural heritage, will be considered.