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PERFORMANCE OF ACIDIC MCM-LIKE ALUMINOSILICATE CATALYSTS IN PYROLYSIS OF POLYPROPYLENE
Mesoporous aluminosilicate catalysts having different Al/Si ratios were synthesized following a hydrothermal synthesis route and using different aluminum sources, such as aluminum nitrate and aluminum isopropoxide. These mesoporous materials have high surface areas, in the range of 520-1001 m 2 /g,...
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Published in: | Chemical engineering communications 2009-01, Vol.196 (1-2), p.116-130 |
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creator | Obali, Zeynep Sezgi, Naime Asli Doğu, Timur |
description | Mesoporous aluminosilicate catalysts having different Al/Si ratios were synthesized following a hydrothermal synthesis route and using different aluminum sources, such as aluminum nitrate and aluminum isopropoxide. These mesoporous materials have high surface areas, in the range of 520-1001 m
2
/g, and exhibit Type IV nitrogen adsorption isotherms. EDS and
27
Al MAS NMR results showed that aluminum was incorporated more effectively into the structure of the catalyst forming a tetrahedral framework when aluminum nitrate was used as the aluminum source. The activities of these catalysts in the polypropylene pyrolysis reaction were tested in a TGA apparatus. Results showed a marked reduction in the degradation temperature in the presence of aluminosilicate catalysts. The activation energy of degradation was 172 kJ/mole without any catalyst. However, using the mesoporous aluminosilicate catalysts synthesized by using aluminum nitrate as the aluminum source, activation energy of the degradation reaction decreased to values of about 24-28 kJ/mole. |
doi_str_mv | 10.1080/00986440802301537 |
format | article |
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2
/g, and exhibit Type IV nitrogen adsorption isotherms. EDS and
27
Al MAS NMR results showed that aluminum was incorporated more effectively into the structure of the catalyst forming a tetrahedral framework when aluminum nitrate was used as the aluminum source. The activities of these catalysts in the polypropylene pyrolysis reaction were tested in a TGA apparatus. Results showed a marked reduction in the degradation temperature in the presence of aluminosilicate catalysts. The activation energy of degradation was 172 kJ/mole without any catalyst. However, using the mesoporous aluminosilicate catalysts synthesized by using aluminum nitrate as the aluminum source, activation energy of the degradation reaction decreased to values of about 24-28 kJ/mole.</description><identifier>ISSN: 0098-6445</identifier><identifier>EISSN: 1563-5201</identifier><identifier>DOI: 10.1080/00986440802301537</identifier><language>eng</language><publisher>Philadelphia: Taylor & Francis Group</publisher><subject>Adsorption ; Aluminosilicate ; Aluminum ; Catalysts ; Catalytic degradation ; Mesoporous catalyst ; Nitrogen ; Polypropylene ; Temperature</subject><ispartof>Chemical engineering communications, 2009-01, Vol.196 (1-2), p.116-130</ispartof><rights>Copyright Taylor & Francis Group, LLC 2008</rights><rights>Copyright Taylor & Francis Ltd. 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-80ad369206930fc8732bb37165f876608d781f92e6bba17dc41aa447626e3bcb3</citedby><cites>FETCH-LOGICAL-c404t-80ad369206930fc8732bb37165f876608d781f92e6bba17dc41aa447626e3bcb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Obali, Zeynep</creatorcontrib><creatorcontrib>Sezgi, Naime Asli</creatorcontrib><creatorcontrib>Doğu, Timur</creatorcontrib><title>PERFORMANCE OF ACIDIC MCM-LIKE ALUMINOSILICATE CATALYSTS IN PYROLYSIS OF POLYPROPYLENE</title><title>Chemical engineering communications</title><description>Mesoporous aluminosilicate catalysts having different Al/Si ratios were synthesized following a hydrothermal synthesis route and using different aluminum sources, such as aluminum nitrate and aluminum isopropoxide. These mesoporous materials have high surface areas, in the range of 520-1001 m
2
/g, and exhibit Type IV nitrogen adsorption isotherms. EDS and
27
Al MAS NMR results showed that aluminum was incorporated more effectively into the structure of the catalyst forming a tetrahedral framework when aluminum nitrate was used as the aluminum source. The activities of these catalysts in the polypropylene pyrolysis reaction were tested in a TGA apparatus. Results showed a marked reduction in the degradation temperature in the presence of aluminosilicate catalysts. The activation energy of degradation was 172 kJ/mole without any catalyst. However, using the mesoporous aluminosilicate catalysts synthesized by using aluminum nitrate as the aluminum source, activation energy of the degradation reaction decreased to values of about 24-28 kJ/mole.</description><subject>Adsorption</subject><subject>Aluminosilicate</subject><subject>Aluminum</subject><subject>Catalysts</subject><subject>Catalytic degradation</subject><subject>Mesoporous catalyst</subject><subject>Nitrogen</subject><subject>Polypropylene</subject><subject>Temperature</subject><issn>0098-6445</issn><issn>1563-5201</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkEtPg0AUhSdGE2v1B7gjLtyhd5hhgMQNQapECgRak64mwyuhoVAHGu2_d5q6solu7iP3fCc3B6FbDA8YbHgEcGxGqRoNAtgk1hmaYJMR3TQAn6PJ4a4rgXmJroZhDYAJwXiC3hM_ncXp3I08X4tnmusFz4Gnzb25HgZvvuaGy3kQxVkQBp678DVV3HCVLTItiLRklcZqCbIDmagxSeNkFfqRf40uatEO1c1Pn6LlzF94r3oYvyijUC8o0FG3QZSEOQYwh0Bd2BYx8pxYmJm1bTEGdmnZuHaMiuW5wFZZUCwEpRYzWEXyIidTdH_03cr-Y1cNI980Q1G1reiqfjdwwijDDnGU8O6XcN3vZKd-44YBANRWiUwRPooK2Q-DrGq-lc1GyD3HwA8x85OYFfN0ZJqu7uVGfPayLfko9m0vaym6olFf_IVb_-InFB-_RvINH02Lhw</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Obali, Zeynep</creator><creator>Sezgi, Naime Asli</creator><creator>Doğu, Timur</creator><general>Taylor & Francis Group</general><general>Taylor & Francis Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7QF</scope><scope>JG9</scope></search><sort><creationdate>20090101</creationdate><title>PERFORMANCE OF ACIDIC MCM-LIKE ALUMINOSILICATE CATALYSTS IN PYROLYSIS OF POLYPROPYLENE</title><author>Obali, Zeynep ; Sezgi, Naime Asli ; Doğu, Timur</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-80ad369206930fc8732bb37165f876608d781f92e6bba17dc41aa447626e3bcb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adsorption</topic><topic>Aluminosilicate</topic><topic>Aluminum</topic><topic>Catalysts</topic><topic>Catalytic degradation</topic><topic>Mesoporous catalyst</topic><topic>Nitrogen</topic><topic>Polypropylene</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Obali, Zeynep</creatorcontrib><creatorcontrib>Sezgi, Naime Asli</creatorcontrib><creatorcontrib>Doğu, Timur</creatorcontrib><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Aluminium Industry Abstracts</collection><collection>Materials Research Database</collection><jtitle>Chemical engineering communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Obali, Zeynep</au><au>Sezgi, Naime Asli</au><au>Doğu, Timur</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PERFORMANCE OF ACIDIC MCM-LIKE ALUMINOSILICATE CATALYSTS IN PYROLYSIS OF POLYPROPYLENE</atitle><jtitle>Chemical engineering communications</jtitle><date>2009-01-01</date><risdate>2009</risdate><volume>196</volume><issue>1-2</issue><spage>116</spage><epage>130</epage><pages>116-130</pages><issn>0098-6445</issn><eissn>1563-5201</eissn><abstract>Mesoporous aluminosilicate catalysts having different Al/Si ratios were synthesized following a hydrothermal synthesis route and using different aluminum sources, such as aluminum nitrate and aluminum isopropoxide. These mesoporous materials have high surface areas, in the range of 520-1001 m
2
/g, and exhibit Type IV nitrogen adsorption isotherms. EDS and
27
Al MAS NMR results showed that aluminum was incorporated more effectively into the structure of the catalyst forming a tetrahedral framework when aluminum nitrate was used as the aluminum source. The activities of these catalysts in the polypropylene pyrolysis reaction were tested in a TGA apparatus. Results showed a marked reduction in the degradation temperature in the presence of aluminosilicate catalysts. The activation energy of degradation was 172 kJ/mole without any catalyst. However, using the mesoporous aluminosilicate catalysts synthesized by using aluminum nitrate as the aluminum source, activation energy of the degradation reaction decreased to values of about 24-28 kJ/mole.</abstract><cop>Philadelphia</cop><pub>Taylor & Francis Group</pub><doi>10.1080/00986440802301537</doi><tpages>15</tpages></addata></record> |
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source | Taylor and Francis Science and Technology Collection |
subjects | Adsorption Aluminosilicate Aluminum Catalysts Catalytic degradation Mesoporous catalyst Nitrogen Polypropylene Temperature |
title | PERFORMANCE OF ACIDIC MCM-LIKE ALUMINOSILICATE CATALYSTS IN PYROLYSIS OF POLYPROPYLENE |
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