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Large scale melt synthesis in an open crucible of Na-fluorohectorite with superb charge homogeneity and particle size
Sodium fluorohectorite Na 0.6[Mg 2.4Li 0.6]Si 4O 10F 2 was synthesized from the melt in an open glassy carbon crucible at 1265 °C under argon flow. A glass (Na 2O–Li 2O–SiO 2) precursor was used as a fluxing agent in order to maintain a low vapor pressure of volatile fluorides and sustain a low sili...
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Published in: | Applied clay science 2010-03, Vol.48 (1), p.39-45 |
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creator | Kalo, Hussein Möller, Michael W. Ziadeh, Mazen Dolejš, David Breu, Josef |
description | Sodium fluorohectorite Na
0.6[Mg
2.4Li
0.6]Si
4O
10F
2 was synthesized from the melt in an open glassy carbon crucible at 1265
°C under argon flow. A glass (Na
2O–Li
2O–SiO
2) precursor was used as a fluxing agent in order to maintain a low vapor pressure of volatile fluorides and sustain a low silica activity, which inhibits the formation of silicon fluoride gases and promotes the fluorine solubility in the melt. To minimize the loss of volatile fluorine compounds the pre-synthesized alkali silicate glass was heated together with additional raw materials needed in a high frequency induction furnace rapidly from 800
°C up to 1265
°C and then kept at this temperature for a short period of time (15
min). The synthesis method can easily be scaled to batches larger than 1
kg. The Na
0.6-fluorohectorite obtained stands out by (i) phase purity as checked by X-ray powder diffraction (PXRD), (ii) a superb homogeneity of the charge density as demonstrated by stepwise hydration behavior followed by in-situ PXRD in a humidity chamber and the Lagaly method with alkylammonium exchange (
Mermut and Lagaly, 2001), (iii) a high cation exchange capacity (CEC) of 136
meq/100
g as determined by the copper complex ([Cu(trien)]
2+) method, and (iv) extreme lateral extensions with a median value of the particle size of 45
μm as measured by static laser light scattering (SLS) which was confirmed by scanning electron microscopy (SEM). |
doi_str_mv | 10.1016/j.clay.2009.11.014 |
format | article |
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0.6[Mg
2.4Li
0.6]Si
4O
10F
2 was synthesized from the melt in an open glassy carbon crucible at 1265
°C under argon flow. A glass (Na
2O–Li
2O–SiO
2) precursor was used as a fluxing agent in order to maintain a low vapor pressure of volatile fluorides and sustain a low silica activity, which inhibits the formation of silicon fluoride gases and promotes the fluorine solubility in the melt. To minimize the loss of volatile fluorine compounds the pre-synthesized alkali silicate glass was heated together with additional raw materials needed in a high frequency induction furnace rapidly from 800
°C up to 1265
°C and then kept at this temperature for a short period of time (15
min). The synthesis method can easily be scaled to batches larger than 1
kg. The Na
0.6-fluorohectorite obtained stands out by (i) phase purity as checked by X-ray powder diffraction (PXRD), (ii) a superb homogeneity of the charge density as demonstrated by stepwise hydration behavior followed by in-situ PXRD in a humidity chamber and the Lagaly method with alkylammonium exchange (
Mermut and Lagaly, 2001), (iii) a high cation exchange capacity (CEC) of 136
meq/100
g as determined by the copper complex ([Cu(trien)]
2+) method, and (iv) extreme lateral extensions with a median value of the particle size of 45
μm as measured by static laser light scattering (SLS) which was confirmed by scanning electron microscopy (SEM).</description><identifier>ISSN: 0169-1317</identifier><identifier>EISSN: 1872-9053</identifier><identifier>DOI: 10.1016/j.clay.2009.11.014</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>CHARGE DENSITY ; Charge homogeneity ; Crucibles ; FABRICATION ; FLUORIDES ; Fluorohectorite ; FLUXING ; Homogeneity ; Large scale synthesis ; Melt synthesis ; Melts ; Particle size ; PARTICLE SIZE AND SHAPE ; SCANNING ELECTRON MICROSCOPY ; Synthesis</subject><ispartof>Applied clay science, 2010-03, Vol.48 (1), p.39-45</ispartof><rights>2009 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c369t-ecfc9fd4b8151a04245d3a67d956576fdec59a560c56835ffa68f6feabceb3c63</citedby><cites>FETCH-LOGICAL-c369t-ecfc9fd4b8151a04245d3a67d956576fdec59a560c56835ffa68f6feabceb3c63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Kalo, Hussein</creatorcontrib><creatorcontrib>Möller, Michael W.</creatorcontrib><creatorcontrib>Ziadeh, Mazen</creatorcontrib><creatorcontrib>Dolejš, David</creatorcontrib><creatorcontrib>Breu, Josef</creatorcontrib><title>Large scale melt synthesis in an open crucible of Na-fluorohectorite with superb charge homogeneity and particle size</title><title>Applied clay science</title><description>Sodium fluorohectorite Na
0.6[Mg
2.4Li
0.6]Si
4O
10F
2 was synthesized from the melt in an open glassy carbon crucible at 1265
°C under argon flow. A glass (Na
2O–Li
2O–SiO
2) precursor was used as a fluxing agent in order to maintain a low vapor pressure of volatile fluorides and sustain a low silica activity, which inhibits the formation of silicon fluoride gases and promotes the fluorine solubility in the melt. To minimize the loss of volatile fluorine compounds the pre-synthesized alkali silicate glass was heated together with additional raw materials needed in a high frequency induction furnace rapidly from 800
°C up to 1265
°C and then kept at this temperature for a short period of time (15
min). The synthesis method can easily be scaled to batches larger than 1
kg. The Na
0.6-fluorohectorite obtained stands out by (i) phase purity as checked by X-ray powder diffraction (PXRD), (ii) a superb homogeneity of the charge density as demonstrated by stepwise hydration behavior followed by in-situ PXRD in a humidity chamber and the Lagaly method with alkylammonium exchange (
Mermut and Lagaly, 2001), (iii) a high cation exchange capacity (CEC) of 136
meq/100
g as determined by the copper complex ([Cu(trien)]
2+) method, and (iv) extreme lateral extensions with a median value of the particle size of 45
μm as measured by static laser light scattering (SLS) which was confirmed by scanning electron microscopy (SEM).</description><subject>CHARGE DENSITY</subject><subject>Charge homogeneity</subject><subject>Crucibles</subject><subject>FABRICATION</subject><subject>FLUORIDES</subject><subject>Fluorohectorite</subject><subject>FLUXING</subject><subject>Homogeneity</subject><subject>Large scale synthesis</subject><subject>Melt synthesis</subject><subject>Melts</subject><subject>Particle size</subject><subject>PARTICLE SIZE AND SHAPE</subject><subject>SCANNING ELECTRON MICROSCOPY</subject><subject>Synthesis</subject><issn>0169-1317</issn><issn>1872-9053</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp9kL1O5DAURi20SMwCL0DlbqsEOx47iUSDEH_SaLdZasu5uSYeZeKs7YCGp8fDUG91m_Md6R5CrjgrOePqelvCaPZlxVhbcl4yvj4hK97UVdEyKX6QVYbaggten5GfMW4Z41Uj2xVZNia8Io1gRqQ7HBON-ykNGF2kbqJmon7GiUJYwHUZ8Zb-NoUdFx_8gJB8cAnpu0sDjcuMoaMwfBkHv_OvOKFL-2zp6WxCcpAN0X3gBTm1Zox4-X3PycvD_d-7p2Lz5_H57nZTgFBtKhAstLZfdw2X3LB1tZa9MKruW6lkrWyPIFsjFQOpGiGtNaqxyqLpADsBSpyTX0fvHPy_BWPSOxcBx9FM6JeoaylqUXMhMlkdSQg-xoBWz8HtTNhrzvQhsd7qQ2J9SKw51zlxHt0cR5h_eHMYdASHE2DvQm6je-_-N_8EUvyIDA</recordid><startdate>20100301</startdate><enddate>20100301</enddate><creator>Kalo, Hussein</creator><creator>Möller, Michael W.</creator><creator>Ziadeh, Mazen</creator><creator>Dolejš, David</creator><creator>Breu, Josef</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QQ</scope><scope>8FD</scope><scope>H8G</scope><scope>JG9</scope></search><sort><creationdate>20100301</creationdate><title>Large scale melt synthesis in an open crucible of Na-fluorohectorite with superb charge homogeneity and particle size</title><author>Kalo, Hussein ; Möller, Michael W. ; Ziadeh, Mazen ; Dolejš, David ; Breu, Josef</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c369t-ecfc9fd4b8151a04245d3a67d956576fdec59a560c56835ffa68f6feabceb3c63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>CHARGE DENSITY</topic><topic>Charge homogeneity</topic><topic>Crucibles</topic><topic>FABRICATION</topic><topic>FLUORIDES</topic><topic>Fluorohectorite</topic><topic>FLUXING</topic><topic>Homogeneity</topic><topic>Large scale synthesis</topic><topic>Melt synthesis</topic><topic>Melts</topic><topic>Particle size</topic><topic>PARTICLE SIZE AND SHAPE</topic><topic>SCANNING ELECTRON MICROSCOPY</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kalo, Hussein</creatorcontrib><creatorcontrib>Möller, Michael W.</creatorcontrib><creatorcontrib>Ziadeh, Mazen</creatorcontrib><creatorcontrib>Dolejš, David</creatorcontrib><creatorcontrib>Breu, Josef</creatorcontrib><collection>CrossRef</collection><collection>Ceramic Abstracts</collection><collection>Technology Research Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><jtitle>Applied clay science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kalo, Hussein</au><au>Möller, Michael W.</au><au>Ziadeh, Mazen</au><au>Dolejš, David</au><au>Breu, Josef</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Large scale melt synthesis in an open crucible of Na-fluorohectorite with superb charge homogeneity and particle size</atitle><jtitle>Applied clay science</jtitle><date>2010-03-01</date><risdate>2010</risdate><volume>48</volume><issue>1</issue><spage>39</spage><epage>45</epage><pages>39-45</pages><issn>0169-1317</issn><eissn>1872-9053</eissn><abstract>Sodium fluorohectorite Na
0.6[Mg
2.4Li
0.6]Si
4O
10F
2 was synthesized from the melt in an open glassy carbon crucible at 1265
°C under argon flow. A glass (Na
2O–Li
2O–SiO
2) precursor was used as a fluxing agent in order to maintain a low vapor pressure of volatile fluorides and sustain a low silica activity, which inhibits the formation of silicon fluoride gases and promotes the fluorine solubility in the melt. To minimize the loss of volatile fluorine compounds the pre-synthesized alkali silicate glass was heated together with additional raw materials needed in a high frequency induction furnace rapidly from 800
°C up to 1265
°C and then kept at this temperature for a short period of time (15
min). The synthesis method can easily be scaled to batches larger than 1
kg. The Na
0.6-fluorohectorite obtained stands out by (i) phase purity as checked by X-ray powder diffraction (PXRD), (ii) a superb homogeneity of the charge density as demonstrated by stepwise hydration behavior followed by in-situ PXRD in a humidity chamber and the Lagaly method with alkylammonium exchange (
Mermut and Lagaly, 2001), (iii) a high cation exchange capacity (CEC) of 136
meq/100
g as determined by the copper complex ([Cu(trien)]
2+) method, and (iv) extreme lateral extensions with a median value of the particle size of 45
μm as measured by static laser light scattering (SLS) which was confirmed by scanning electron microscopy (SEM).</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.clay.2009.11.014</doi><tpages>7</tpages></addata></record> |
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language | eng |
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source | ScienceDirect Journals |
subjects | CHARGE DENSITY Charge homogeneity Crucibles FABRICATION FLUORIDES Fluorohectorite FLUXING Homogeneity Large scale synthesis Melt synthesis Melts Particle size PARTICLE SIZE AND SHAPE SCANNING ELECTRON MICROSCOPY Synthesis |
title | Large scale melt synthesis in an open crucible of Na-fluorohectorite with superb charge homogeneity and particle size |
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