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Cation and anion ordering in synthetic lepidolites and lithian muscovites: influence of the OH ∕ F and Li ∕ Al ratios on the mica formation studied by NMR (nuclear magnetic resonance) spectroscopy and X-ray diffraction

A large number of lepidolites K(LixAl3−x)[Si2xAl4−2xO10](OH)yF2−y and Li-muscovites K(LixAl2-x/3□1-2x/3)[Si3AlO10](OH)yF2−y were synthesised by a gelling method in combination with hydrothermal syntheses at a pressure of 2 kbar and a temperature of 873 K. The nominal composition ranged between 0.0≤x...

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Published in:European journal of mineralogy (Stuttgart) 2023-03, Vol.35 (2), p.199-217
Main Authors: Sulcek, Lara, Marler, Bernd, Fechtelkord, Michael
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description A large number of lepidolites K(LixAl3−x)[Si2xAl4−2xO10](OH)yF2−y and Li-muscovites K(LixAl2-x/3□1-2x/3)[Si3AlO10](OH)yF2−y were synthesised by a gelling method in combination with hydrothermal syntheses at a pressure of 2 kbar and a temperature of 873 K. The nominal composition ranged between 0.0≤x≤2.0 and 0.0≤y≤2.0, i.e. from polylithionite K[Li2.0Al][Si4.0O10](OH)yF2−y over trilithionite K[Li1.5Al1.5][AlSi3.0O10](OH)yF2−y to muscovite K[Al2.0□][AlSi3.0O10](OH)yF2−y. 1H, 19F, 29Si and 27Al magic-angle spinning nuclear magnetic resonance (MAS NMR) and 27Al multiple-quantum magic-angle spinning (MQMAS) NMR spectroscopy has been performed to investigate the order and/or disorder state of Si and Al in the tetrahedral layers and of Li, Al, OH and F in the octahedral layer. The synthetic mica crystals are very small, ranging from 0.1 to 5 µm. With increasing Al content, the crystal sizes decrease. Rietveld structure analyses on 12 samples showed that nearly all samples consist of two mica polytypes (1M and 2M1) of varying proportions. In the case of lepidolites, the 1M / 2M1 ratio depends on the Li/Al ratio of the reaction mixture. The refinement of the occupancy factors of octahedral sites shows that lepidolites (1.5≤x≤2.0) represent a solid solution series with polylithionite and trilithionite as the endmembers. In the case of the Li-muscovites (0.0≤x≤1.5), the 1M / 2M1 ratio depends on the number of impurity phases like eucryptite or sanidine depleting the reaction mixture of Li or Al. There is no solid solution between trilithionite and muscovite; instead, the Li-muscovite crystals consist of domains differing in the relative proportions of muscovite and trilithionite. The overall composition of the synthesised micas which consist of two polytypes can be characterised by 29Si, 1H and 19F MAS NMR spectroscopy. The Si/Al ratio in the tetrahedral layers and thus the content of [4]Al were calculated by analysing the signal intensities of the 29Si MAS NMR experiments. The Li content xest was calculated from the measured tetrahedral Si/Al ratio of the 29Si MAS NMR signals. The calculated Li contents xest of samples between polylithionite and trilithionite agree with the expected values. The F-rich samples show slightly increased values and the OH samples lower values. Lepidolites with only F (x = 1.5 to 2.0, y = 0.0), but not lepidolites with only OH (x = 1.5 to 2.0 and y = 2.0), were observed after synthesis. With decreasing Li content, x≤1.2, Li-muscovites con
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The nominal composition ranged between 0.0≤x≤2.0 and 0.0≤y≤2.0, i.e. from polylithionite K[Li2.0Al][Si4.0O10](OH)yF2−y over trilithionite K[Li1.5Al1.5][AlSi3.0O10](OH)yF2−y to muscovite K[Al2.0□][AlSi3.0O10](OH)yF2−y. 1H, 19F, 29Si and 27Al magic-angle spinning nuclear magnetic resonance (MAS NMR) and 27Al multiple-quantum magic-angle spinning (MQMAS) NMR spectroscopy has been performed to investigate the order and/or disorder state of Si and Al in the tetrahedral layers and of Li, Al, OH and F in the octahedral layer. The synthetic mica crystals are very small, ranging from 0.1 to 5 µm. With increasing Al content, the crystal sizes decrease. Rietveld structure analyses on 12 samples showed that nearly all samples consist of two mica polytypes (1M and 2M1) of varying proportions. In the case of lepidolites, the 1M / 2M1 ratio depends on the Li/Al ratio of the reaction mixture. The refinement of the occupancy factors of octahedral sites shows that lepidolites (1.5≤x≤2.0) represent a solid solution series with polylithionite and trilithionite as the endmembers. In the case of the Li-muscovites (0.0≤x≤1.5), the 1M / 2M1 ratio depends on the number of impurity phases like eucryptite or sanidine depleting the reaction mixture of Li or Al. There is no solid solution between trilithionite and muscovite; instead, the Li-muscovite crystals consist of domains differing in the relative proportions of muscovite and trilithionite. The overall composition of the synthesised micas which consist of two polytypes can be characterised by 29Si, 1H and 19F MAS NMR spectroscopy. The Si/Al ratio in the tetrahedral layers and thus the content of [4]Al were calculated by analysing the signal intensities of the 29Si MAS NMR experiments. The Li content xest was calculated from the measured tetrahedral Si/Al ratio of the 29Si MAS NMR signals. The calculated Li contents xest of samples between polylithionite and trilithionite agree with the expected values. The F-rich samples show slightly increased values and the OH samples lower values. Lepidolites with only F (x = 1.5 to 2.0, y = 0.0), but not lepidolites with only OH (x = 1.5 to 2.0 and y = 2.0), were observed after synthesis. With decreasing Li content, x≤1.2, Li-muscovites containing mostly hydroxyl (y&gt;1.0) are formed. It was possible to synthesise fluorine containing micas with a Li content as low as 0.3 and y = 0.2 to 1.8. The 19F and 1H MAS NMR experiments reveal that F and OH are not distributed statistically but local structural preferences exist. F is attracted by Li-rich and OH by Al-rich environments. The quadrupolar coupling constant which represents the anisotropy of the Al coordination is low for polylithionite with CQ=1.5 MHz and increases to CQ=3.8 MHz for trilithionite. For tetrahedral Al a smaller increase of CQ from 1.7 to 2.8 MHz is observed. Advancing from trilithionite to muscovite both quadrupolar coupling constants decrease to 2.5 MHz for octahedral and 1.5 MHz for tetrahedral Al. In polylithionite there is the most isotropic environment for octahedral Al; there are only Li2Al sites coordinated by F in the octahedral sheets and O from the tetrahedral sheets which are regular, containing only Si. The distortion and anisotropy for Al in tetrahedral as well as octahedral sheets increases with rising Al content. The most anisotropic environment can be found in trilithionite, especially for octahedral Al.</description><identifier>ISSN: 1617-4011</identifier><identifier>ISSN: 0935-1221</identifier><identifier>EISSN: 1617-4011</identifier><identifier>DOI: 10.5194/ejm-35-199-2023</identifier><language>eng</language><publisher>Göttingen: Copernicus GmbH</publisher><subject>Aluminum ; Anisotropy ; Composition ; Coupling ; Crystal structure ; Crystals ; Eucryptite ; Fluorine ; Investigations ; Lithium ; Mathematical analysis ; Mica ; Mineralogical research ; Minerals ; Mixtures ; Muscovite ; NMR ; NMR spectroscopy ; Nuclear magnetic resonance ; Nuclear magnetic resonance spectroscopy ; Polytypes ; Sheets ; Silicon ; Solid solutions ; Spectroscopy ; Spectrum analysis ; Testing ; X-ray diffraction</subject><ispartof>European journal of mineralogy (Stuttgart), 2023-03, Vol.35 (2), p.199-217</ispartof><rights>COPYRIGHT 2023 Copernicus GmbH</rights><rights>2023. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-d36b282749dbf78e99ac75d32cc7e88d13bcc78030084dd7d5467dd5c8eba9953</citedby><cites>FETCH-LOGICAL-c415t-d36b282749dbf78e99ac75d32cc7e88d13bcc78030084dd7d5467dd5c8eba9953</cites><orcidid>0000-0003-1938-1547</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2792266008/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2792266008?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,864,2102,25753,27924,27925,37012,44590,75126</link.rule.ids></links><search><creatorcontrib>Sulcek, Lara</creatorcontrib><creatorcontrib>Marler, Bernd</creatorcontrib><creatorcontrib>Fechtelkord, Michael</creatorcontrib><title>Cation and anion ordering in synthetic lepidolites and lithian muscovites: influence of the OH ∕ F and Li ∕ Al ratios on the mica formation studied by NMR (nuclear magnetic resonance) spectroscopy and X-ray diffraction</title><title>European journal of mineralogy (Stuttgart)</title><description>A large number of lepidolites K(LixAl3−x)[Si2xAl4−2xO10](OH)yF2−y and Li-muscovites K(LixAl2-x/3□1-2x/3)[Si3AlO10](OH)yF2−y were synthesised by a gelling method in combination with hydrothermal syntheses at a pressure of 2 kbar and a temperature of 873 K. The nominal composition ranged between 0.0≤x≤2.0 and 0.0≤y≤2.0, i.e. from polylithionite K[Li2.0Al][Si4.0O10](OH)yF2−y over trilithionite K[Li1.5Al1.5][AlSi3.0O10](OH)yF2−y to muscovite K[Al2.0□][AlSi3.0O10](OH)yF2−y. 1H, 19F, 29Si and 27Al magic-angle spinning nuclear magnetic resonance (MAS NMR) and 27Al multiple-quantum magic-angle spinning (MQMAS) NMR spectroscopy has been performed to investigate the order and/or disorder state of Si and Al in the tetrahedral layers and of Li, Al, OH and F in the octahedral layer. The synthetic mica crystals are very small, ranging from 0.1 to 5 µm. With increasing Al content, the crystal sizes decrease. Rietveld structure analyses on 12 samples showed that nearly all samples consist of two mica polytypes (1M and 2M1) of varying proportions. In the case of lepidolites, the 1M / 2M1 ratio depends on the Li/Al ratio of the reaction mixture. The refinement of the occupancy factors of octahedral sites shows that lepidolites (1.5≤x≤2.0) represent a solid solution series with polylithionite and trilithionite as the endmembers. In the case of the Li-muscovites (0.0≤x≤1.5), the 1M / 2M1 ratio depends on the number of impurity phases like eucryptite or sanidine depleting the reaction mixture of Li or Al. There is no solid solution between trilithionite and muscovite; instead, the Li-muscovite crystals consist of domains differing in the relative proportions of muscovite and trilithionite. The overall composition of the synthesised micas which consist of two polytypes can be characterised by 29Si, 1H and 19F MAS NMR spectroscopy. The Si/Al ratio in the tetrahedral layers and thus the content of [4]Al were calculated by analysing the signal intensities of the 29Si MAS NMR experiments. The Li content xest was calculated from the measured tetrahedral Si/Al ratio of the 29Si MAS NMR signals. The calculated Li contents xest of samples between polylithionite and trilithionite agree with the expected values. The F-rich samples show slightly increased values and the OH samples lower values. Lepidolites with only F (x = 1.5 to 2.0, y = 0.0), but not lepidolites with only OH (x = 1.5 to 2.0 and y = 2.0), were observed after synthesis. With decreasing Li content, x≤1.2, Li-muscovites containing mostly hydroxyl (y&gt;1.0) are formed. It was possible to synthesise fluorine containing micas with a Li content as low as 0.3 and y = 0.2 to 1.8. The 19F and 1H MAS NMR experiments reveal that F and OH are not distributed statistically but local structural preferences exist. F is attracted by Li-rich and OH by Al-rich environments. The quadrupolar coupling constant which represents the anisotropy of the Al coordination is low for polylithionite with CQ=1.5 MHz and increases to CQ=3.8 MHz for trilithionite. For tetrahedral Al a smaller increase of CQ from 1.7 to 2.8 MHz is observed. Advancing from trilithionite to muscovite both quadrupolar coupling constants decrease to 2.5 MHz for octahedral and 1.5 MHz for tetrahedral Al. In polylithionite there is the most isotropic environment for octahedral Al; there are only Li2Al sites coordinated by F in the octahedral sheets and O from the tetrahedral sheets which are regular, containing only Si. The distortion and anisotropy for Al in tetrahedral as well as octahedral sheets increases with rising Al content. The most anisotropic environment can be found in trilithionite, especially for octahedral Al.</description><subject>Aluminum</subject><subject>Anisotropy</subject><subject>Composition</subject><subject>Coupling</subject><subject>Crystal structure</subject><subject>Crystals</subject><subject>Eucryptite</subject><subject>Fluorine</subject><subject>Investigations</subject><subject>Lithium</subject><subject>Mathematical analysis</subject><subject>Mica</subject><subject>Mineralogical research</subject><subject>Minerals</subject><subject>Mixtures</subject><subject>Muscovite</subject><subject>NMR</subject><subject>NMR spectroscopy</subject><subject>Nuclear magnetic resonance</subject><subject>Nuclear magnetic resonance spectroscopy</subject><subject>Polytypes</subject><subject>Sheets</subject><subject>Silicon</subject><subject>Solid solutions</subject><subject>Spectroscopy</subject><subject>Spectrum analysis</subject><subject>Testing</subject><subject>X-ray diffraction</subject><issn>1617-4011</issn><issn>0935-1221</issn><issn>1617-4011</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpNUl2L1DAULaLguvrsa8AXfehu89Gm8W0YXHdhdEEUfAtpcjuboU3GpBXmH_gH_Hs--Eu87YhICT253HPuyeUUxUtaXdVUiWs4jCWvS6pUySrGHxUXtKGyFBWlj__DT4tnOR-qinIhqovi19ZMPgZigsOzoJgcJB_2xAeST2F6gMlbMsDRuzj4CfLai-jBm0DGOdv4fSm_RUI_zBAskNgT5JH7W_L7x09yszJ2fr1sBpKWkZngrKVp9NaQPqbxbCRPs_PgSHciHz98Iq_DbAcwiYxmH1YnCXIMBqe8IfkIdkoRHRxP64yvZTIn4nzfJ2MXuefFk94MGV78_V8WX27efd7elrv793fbza60gtZT6XjTsZZJoVzXyxaUMlbWjjNrJbSto7xD1Fa8qlrhnHS1aKRztW2hM0rV_LK4O-u6aA76mPxo0klH4_VaiGmvTUL3A2ipGqaglhwkFcIw0xpnOtnb1gohHEOtV2etY4rfZsiTPsQ5BbSvmVSMNQ26wK6rc9feoCiuPk74Zvwc4EZjgN5jfSMFb0RTtxIJ12eCxY3lBP0_m7TSS4I0JkjzWmOC9JIg_gdeur5n</recordid><startdate>20230330</startdate><enddate>20230330</enddate><creator>Sulcek, Lara</creator><creator>Marler, Bernd</creator><creator>Fechtelkord, Michael</creator><general>Copernicus GmbH</general><general>Copernicus Publications</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8BQ</scope><scope>8FD</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>PCBAR</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-1938-1547</orcidid></search><sort><creationdate>20230330</creationdate><title>Cation and anion ordering in synthetic lepidolites and lithian muscovites: influence of the OH ∕ F and Li ∕ Al ratios on the mica formation studied by NMR (nuclear magnetic resonance) spectroscopy and X-ray diffraction</title><author>Sulcek, Lara ; Marler, Bernd ; Fechtelkord, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-d36b282749dbf78e99ac75d32cc7e88d13bcc78030084dd7d5467dd5c8eba9953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Aluminum</topic><topic>Anisotropy</topic><topic>Composition</topic><topic>Coupling</topic><topic>Crystal structure</topic><topic>Crystals</topic><topic>Eucryptite</topic><topic>Fluorine</topic><topic>Investigations</topic><topic>Lithium</topic><topic>Mathematical analysis</topic><topic>Mica</topic><topic>Mineralogical research</topic><topic>Minerals</topic><topic>Mixtures</topic><topic>Muscovite</topic><topic>NMR</topic><topic>NMR spectroscopy</topic><topic>Nuclear magnetic resonance</topic><topic>Nuclear magnetic resonance spectroscopy</topic><topic>Polytypes</topic><topic>Sheets</topic><topic>Silicon</topic><topic>Solid solutions</topic><topic>Spectroscopy</topic><topic>Spectrum analysis</topic><topic>Testing</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sulcek, Lara</creatorcontrib><creatorcontrib>Marler, Bernd</creatorcontrib><creatorcontrib>Fechtelkord, Michael</creatorcontrib><collection>CrossRef</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Earth, Atmospheric &amp; Aquatic Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>Materials Research Database</collection><collection>Earth, Atmospheric &amp; Aquatic Science Database</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Directory of Open Access Journals</collection><jtitle>European journal of mineralogy (Stuttgart)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sulcek, Lara</au><au>Marler, Bernd</au><au>Fechtelkord, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cation and anion ordering in synthetic lepidolites and lithian muscovites: influence of the OH ∕ F and Li ∕ Al ratios on the mica formation studied by NMR (nuclear magnetic resonance) spectroscopy and X-ray diffraction</atitle><jtitle>European journal of mineralogy (Stuttgart)</jtitle><date>2023-03-30</date><risdate>2023</risdate><volume>35</volume><issue>2</issue><spage>199</spage><epage>217</epage><pages>199-217</pages><issn>1617-4011</issn><issn>0935-1221</issn><eissn>1617-4011</eissn><abstract>A large number of lepidolites K(LixAl3−x)[Si2xAl4−2xO10](OH)yF2−y and Li-muscovites K(LixAl2-x/3□1-2x/3)[Si3AlO10](OH)yF2−y were synthesised by a gelling method in combination with hydrothermal syntheses at a pressure of 2 kbar and a temperature of 873 K. The nominal composition ranged between 0.0≤x≤2.0 and 0.0≤y≤2.0, i.e. from polylithionite K[Li2.0Al][Si4.0O10](OH)yF2−y over trilithionite K[Li1.5Al1.5][AlSi3.0O10](OH)yF2−y to muscovite K[Al2.0□][AlSi3.0O10](OH)yF2−y. 1H, 19F, 29Si and 27Al magic-angle spinning nuclear magnetic resonance (MAS NMR) and 27Al multiple-quantum magic-angle spinning (MQMAS) NMR spectroscopy has been performed to investigate the order and/or disorder state of Si and Al in the tetrahedral layers and of Li, Al, OH and F in the octahedral layer. The synthetic mica crystals are very small, ranging from 0.1 to 5 µm. With increasing Al content, the crystal sizes decrease. Rietveld structure analyses on 12 samples showed that nearly all samples consist of two mica polytypes (1M and 2M1) of varying proportions. In the case of lepidolites, the 1M / 2M1 ratio depends on the Li/Al ratio of the reaction mixture. The refinement of the occupancy factors of octahedral sites shows that lepidolites (1.5≤x≤2.0) represent a solid solution series with polylithionite and trilithionite as the endmembers. In the case of the Li-muscovites (0.0≤x≤1.5), the 1M / 2M1 ratio depends on the number of impurity phases like eucryptite or sanidine depleting the reaction mixture of Li or Al. There is no solid solution between trilithionite and muscovite; instead, the Li-muscovite crystals consist of domains differing in the relative proportions of muscovite and trilithionite. The overall composition of the synthesised micas which consist of two polytypes can be characterised by 29Si, 1H and 19F MAS NMR spectroscopy. The Si/Al ratio in the tetrahedral layers and thus the content of [4]Al were calculated by analysing the signal intensities of the 29Si MAS NMR experiments. The Li content xest was calculated from the measured tetrahedral Si/Al ratio of the 29Si MAS NMR signals. The calculated Li contents xest of samples between polylithionite and trilithionite agree with the expected values. The F-rich samples show slightly increased values and the OH samples lower values. Lepidolites with only F (x = 1.5 to 2.0, y = 0.0), but not lepidolites with only OH (x = 1.5 to 2.0 and y = 2.0), were observed after synthesis. With decreasing Li content, x≤1.2, Li-muscovites containing mostly hydroxyl (y&gt;1.0) are formed. It was possible to synthesise fluorine containing micas with a Li content as low as 0.3 and y = 0.2 to 1.8. The 19F and 1H MAS NMR experiments reveal that F and OH are not distributed statistically but local structural preferences exist. F is attracted by Li-rich and OH by Al-rich environments. The quadrupolar coupling constant which represents the anisotropy of the Al coordination is low for polylithionite with CQ=1.5 MHz and increases to CQ=3.8 MHz for trilithionite. For tetrahedral Al a smaller increase of CQ from 1.7 to 2.8 MHz is observed. Advancing from trilithionite to muscovite both quadrupolar coupling constants decrease to 2.5 MHz for octahedral and 1.5 MHz for tetrahedral Al. In polylithionite there is the most isotropic environment for octahedral Al; there are only Li2Al sites coordinated by F in the octahedral sheets and O from the tetrahedral sheets which are regular, containing only Si. The distortion and anisotropy for Al in tetrahedral as well as octahedral sheets increases with rising Al content. The most anisotropic environment can be found in trilithionite, especially for octahedral Al.</abstract><cop>Göttingen</cop><pub>Copernicus GmbH</pub><doi>10.5194/ejm-35-199-2023</doi><tpages>19</tpages><orcidid>https://orcid.org/0000-0003-1938-1547</orcidid><oa>free_for_read</oa></addata></record>
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1617-4011
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_79629e573e7144a2a8adab7fc8c444d2
source Publicly Available Content Database (Proquest) (PQ_SDU_P3); Directory of Open Access Journals
subjects Aluminum
Anisotropy
Composition
Coupling
Crystal structure
Crystals
Eucryptite
Fluorine
Investigations
Lithium
Mathematical analysis
Mica
Mineralogical research
Minerals
Mixtures
Muscovite
NMR
NMR spectroscopy
Nuclear magnetic resonance
Nuclear magnetic resonance spectroscopy
Polytypes
Sheets
Silicon
Solid solutions
Spectroscopy
Spectrum analysis
Testing
X-ray diffraction
title Cation and anion ordering in synthetic lepidolites and lithian muscovites: influence of the OH ∕ F and Li ∕ Al ratios on the mica formation studied by NMR (nuclear magnetic resonance) spectroscopy and X-ray diffraction
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