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Acidic medium synthesis of zeolites - an avenue to control the structure-directing power of organic templates
This paper deals with the extension of the synthesis field of microporous zeolite-type materials and types of organic structure-directing agents (OSDA) that can be used to promote their crystallization. The highly hydrophilic hexamethylenetetramine (urotropine), with its C/N ratio = 1.5, which is un...
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Published in: | Dalton transactions : an international journal of inorganic chemistry 2022-08, Vol.51 (3), p.11499-1156 |
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container_start_page | 11499 |
container_title | Dalton transactions : an international journal of inorganic chemistry |
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creator | Fu, Guangying Dib, Eddy Lang, Qiaolin Zhao, Haonuan Wang, Songxia Ding, Ruiqin Yang, Xiaobo Valtchev, Valentin |
description | This paper deals with the extension of the synthesis field of microporous zeolite-type materials and types of organic structure-directing agents (OSDA) that can be used to promote their crystallization. The highly hydrophilic hexamethylenetetramine (urotropine), with its C/N ratio = 1.5, which is unusual to act as a structure-directing agent in the crystallization of open-framework silica polymorphs, is used to exemplify the novelty of the employed approach. Namely, the protonation of urotropine in an acidic fluorine-containing medium transforms it into a very efficient OSDA that yields dodecasil 3C (
MTN
-type). This novel synthesis also allows gaining insights into OSDA-framework interactions in the
MTN
-type structure. The comprehensive
29
Si and
19
F MAS NMR indicate a small number of point defects of the framework T sites and the multiple bonding of F
−
ions to Si in a disordered manner. Based on this finding, a unit cell model has been generated using Monte Carlo simulation and validated with Rietveld refinement using experimental powder X-ray diffraction data. In the model, protonated urotropine cations are located in the center of the big hexakaidecahedral [5
12
6
4
] cages at full occupancy with random orientations. The charge balance is provided by the disordered F
−
ions.
The acidic-medium protonated urotropine acts as a structure-directing agent for crystallizing |HMTA
+
8
,F
−
∼4
|[Si
136(1-2%)
O
272
]-dodecasil 3C-
MTN
and is located in the big [5
12
6
4
] cage. |
doi_str_mv | 10.1039/d2dt01554d |
format | article |
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MTN
-type). This novel synthesis also allows gaining insights into OSDA-framework interactions in the
MTN
-type structure. The comprehensive
29
Si and
19
F MAS NMR indicate a small number of point defects of the framework T sites and the multiple bonding of F
−
ions to Si in a disordered manner. Based on this finding, a unit cell model has been generated using Monte Carlo simulation and validated with Rietveld refinement using experimental powder X-ray diffraction data. In the model, protonated urotropine cations are located in the center of the big hexakaidecahedral [5
12
6
4
] cages at full occupancy with random orientations. The charge balance is provided by the disordered F
−
ions.
The acidic-medium protonated urotropine acts as a structure-directing agent for crystallizing |HMTA
+
8
,F
−
∼4
|[Si
136(1-2%)
O
272
]-dodecasil 3C-
MTN
and is located in the big [5
12
6
4
] cage.</description><identifier>ISSN: 1477-9226</identifier><identifier>EISSN: 1477-9234</identifier><identifier>DOI: 10.1039/d2dt01554d</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Chemical Sciences ; Crystal defects ; Crystallization ; Fluorine ; Hexamethylenetetramine ; Material chemistry ; Monte Carlo simulation ; NMR spectroscopy ; Point defects ; Protonation ; Silicon ; Synthesis ; Unit cell ; X ray powder diffraction ; Zeolites</subject><ispartof>Dalton transactions : an international journal of inorganic chemistry, 2022-08, Vol.51 (3), p.11499-1156</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-d2ac6f601ed30094d04d356e121ec392dd2ab0bfe301219ea0c6968d1d6bfab63</citedby><cites>FETCH-LOGICAL-c384t-d2ac6f601ed30094d04d356e121ec392dd2ab0bfe301219ea0c6968d1d6bfab63</cites><orcidid>0000-0001-6062-3128 ; 0000-0001-9373-8685 ; 0000-0002-2341-6397</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://hal.science/hal-03779241$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Fu, Guangying</creatorcontrib><creatorcontrib>Dib, Eddy</creatorcontrib><creatorcontrib>Lang, Qiaolin</creatorcontrib><creatorcontrib>Zhao, Haonuan</creatorcontrib><creatorcontrib>Wang, Songxia</creatorcontrib><creatorcontrib>Ding, Ruiqin</creatorcontrib><creatorcontrib>Yang, Xiaobo</creatorcontrib><creatorcontrib>Valtchev, Valentin</creatorcontrib><title>Acidic medium synthesis of zeolites - an avenue to control the structure-directing power of organic templates</title><title>Dalton transactions : an international journal of inorganic chemistry</title><description>This paper deals with the extension of the synthesis field of microporous zeolite-type materials and types of organic structure-directing agents (OSDA) that can be used to promote their crystallization. The highly hydrophilic hexamethylenetetramine (urotropine), with its C/N ratio = 1.5, which is unusual to act as a structure-directing agent in the crystallization of open-framework silica polymorphs, is used to exemplify the novelty of the employed approach. Namely, the protonation of urotropine in an acidic fluorine-containing medium transforms it into a very efficient OSDA that yields dodecasil 3C (
MTN
-type). This novel synthesis also allows gaining insights into OSDA-framework interactions in the
MTN
-type structure. The comprehensive
29
Si and
19
F MAS NMR indicate a small number of point defects of the framework T sites and the multiple bonding of F
−
ions to Si in a disordered manner. Based on this finding, a unit cell model has been generated using Monte Carlo simulation and validated with Rietveld refinement using experimental powder X-ray diffraction data. In the model, protonated urotropine cations are located in the center of the big hexakaidecahedral [5
12
6
4
] cages at full occupancy with random orientations. The charge balance is provided by the disordered F
−
ions.
The acidic-medium protonated urotropine acts as a structure-directing agent for crystallizing |HMTA
+
8
,F
−
∼4
|[Si
136(1-2%)
O
272
]-dodecasil 3C-
MTN
and is located in the big [5
12
6
4
] cage.</description><subject>Chemical Sciences</subject><subject>Crystal defects</subject><subject>Crystallization</subject><subject>Fluorine</subject><subject>Hexamethylenetetramine</subject><subject>Material chemistry</subject><subject>Monte Carlo simulation</subject><subject>NMR spectroscopy</subject><subject>Point defects</subject><subject>Protonation</subject><subject>Silicon</subject><subject>Synthesis</subject><subject>Unit cell</subject><subject>X ray powder diffraction</subject><subject>Zeolites</subject><issn>1477-9226</issn><issn>1477-9234</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpd0c1LwzAYBvAgCur04l0IeFGhmo82XY5j8wsGXua5ZMnbGWmbmaQT_evNrEzwkoSXHw95eRA6o-SGEi5vDTOR0KLIzR46onlZZpLxfH_3ZuIQHYfwRghjpGBHqJ1oa6zGLRjbtzh8dvEVgg3Y1fgLXGMjBJxh1WG1ga4HHB3WroveNThJHKLvdew9ZMZ60NF2K7x2H-C3Ac6vVJfCI7TrRqWkE3RQqybA6e89Qi_3d4vpYzZ_fniaTuaZ5uM8ZoYpLWpBKBhOiMwNyQ0vBFBGQXPJTAJLsqyBkzSSoIgWUowNNWJZq6XgI3Q15L6qplp72yr_WTllq8fJvNrOCC9LyXK6ocleDnbt3XsPIVatDRqaRnXg-lAxMZaiTCdL9OIffXO979ImScmSiLJILYzQ9aC0dyF4qHc_oKTatlTN2Gzx09Is4fMB-6B37q9F_g02fY7D</recordid><startdate>20220802</startdate><enddate>20220802</enddate><creator>Fu, Guangying</creator><creator>Dib, Eddy</creator><creator>Lang, Qiaolin</creator><creator>Zhao, Haonuan</creator><creator>Wang, Songxia</creator><creator>Ding, Ruiqin</creator><creator>Yang, Xiaobo</creator><creator>Valtchev, Valentin</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0001-6062-3128</orcidid><orcidid>https://orcid.org/0000-0001-9373-8685</orcidid><orcidid>https://orcid.org/0000-0002-2341-6397</orcidid></search><sort><creationdate>20220802</creationdate><title>Acidic medium synthesis of zeolites - an avenue to control the structure-directing power of organic templates</title><author>Fu, Guangying ; Dib, Eddy ; Lang, Qiaolin ; Zhao, Haonuan ; Wang, Songxia ; Ding, Ruiqin ; Yang, Xiaobo ; Valtchev, Valentin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-d2ac6f601ed30094d04d356e121ec392dd2ab0bfe301219ea0c6968d1d6bfab63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Chemical Sciences</topic><topic>Crystal defects</topic><topic>Crystallization</topic><topic>Fluorine</topic><topic>Hexamethylenetetramine</topic><topic>Material chemistry</topic><topic>Monte Carlo simulation</topic><topic>NMR spectroscopy</topic><topic>Point defects</topic><topic>Protonation</topic><topic>Silicon</topic><topic>Synthesis</topic><topic>Unit cell</topic><topic>X ray powder diffraction</topic><topic>Zeolites</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fu, Guangying</creatorcontrib><creatorcontrib>Dib, Eddy</creatorcontrib><creatorcontrib>Lang, Qiaolin</creatorcontrib><creatorcontrib>Zhao, Haonuan</creatorcontrib><creatorcontrib>Wang, Songxia</creatorcontrib><creatorcontrib>Ding, Ruiqin</creatorcontrib><creatorcontrib>Yang, Xiaobo</creatorcontrib><creatorcontrib>Valtchev, Valentin</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fu, Guangying</au><au>Dib, Eddy</au><au>Lang, Qiaolin</au><au>Zhao, Haonuan</au><au>Wang, Songxia</au><au>Ding, Ruiqin</au><au>Yang, Xiaobo</au><au>Valtchev, Valentin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acidic medium synthesis of zeolites - an avenue to control the structure-directing power of organic templates</atitle><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle><date>2022-08-02</date><risdate>2022</risdate><volume>51</volume><issue>3</issue><spage>11499</spage><epage>1156</epage><pages>11499-1156</pages><issn>1477-9226</issn><eissn>1477-9234</eissn><abstract>This paper deals with the extension of the synthesis field of microporous zeolite-type materials and types of organic structure-directing agents (OSDA) that can be used to promote their crystallization. The highly hydrophilic hexamethylenetetramine (urotropine), with its C/N ratio = 1.5, which is unusual to act as a structure-directing agent in the crystallization of open-framework silica polymorphs, is used to exemplify the novelty of the employed approach. Namely, the protonation of urotropine in an acidic fluorine-containing medium transforms it into a very efficient OSDA that yields dodecasil 3C (
MTN
-type). This novel synthesis also allows gaining insights into OSDA-framework interactions in the
MTN
-type structure. The comprehensive
29
Si and
19
F MAS NMR indicate a small number of point defects of the framework T sites and the multiple bonding of F
−
ions to Si in a disordered manner. Based on this finding, a unit cell model has been generated using Monte Carlo simulation and validated with Rietveld refinement using experimental powder X-ray diffraction data. In the model, protonated urotropine cations are located in the center of the big hexakaidecahedral [5
12
6
4
] cages at full occupancy with random orientations. The charge balance is provided by the disordered F
−
ions.
The acidic-medium protonated urotropine acts as a structure-directing agent for crystallizing |HMTA
+
8
,F
−
∼4
|[Si
136(1-2%)
O
272
]-dodecasil 3C-
MTN
and is located in the big [5
12
6
4
] cage.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d2dt01554d</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-6062-3128</orcidid><orcidid>https://orcid.org/0000-0001-9373-8685</orcidid><orcidid>https://orcid.org/0000-0002-2341-6397</orcidid><oa>free_for_read</oa></addata></record> |
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identifier | ISSN: 1477-9226 |
ispartof | Dalton transactions : an international journal of inorganic chemistry, 2022-08, Vol.51 (3), p.11499-1156 |
issn | 1477-9226 1477-9234 |
language | eng |
recordid | cdi_hal_primary_oai_HAL_hal_03779241v1 |
source | Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list) |
subjects | Chemical Sciences Crystal defects Crystallization Fluorine Hexamethylenetetramine Material chemistry Monte Carlo simulation NMR spectroscopy Point defects Protonation Silicon Synthesis Unit cell X ray powder diffraction Zeolites |
title | Acidic medium synthesis of zeolites - an avenue to control the structure-directing power of organic templates |
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