ZSM-5 fast synthesis employing soluble starch as template
- Autores
- Bonetto, Luciana; Renzini, María Soledad; Saux, Clara; Pierella, Liliana Beatriz
- Año de publicación
- 2017
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión publicada
- Descripción
- Solid catalysts with a zeolitic framework were synthesized in the ZSM-5 (MFI) topology employing tetrapropyl ammonium hydroxide (TPAOH) as structure directing agent and soluble starch as template in order to be employed in biomass revalorization reactions. It should be noted that starch is a soluble, biodegradable, low cost and nontoxic polymeric carbohydrate obtained from agricultural raw materials. Starch is employed in thissynthesis processfor pores generation and crystal connection to produce a material with MFI morphology type. ZSM-5 is a medium pore material from the pentasil zeolites group. The traditional synthesis procedure [1] takes around 10 days to obtain the MFI structure. In this new procedure, ZSM-5 type material is obtained by a hydrothermal treatment but in a shorter crystallization time. The effect of time on structure and cristallinity was studied. Zeolite synthesis was done employing sodium aluminate (NaAlO2) as aluminum source, tetraethyl orthosilicate (TEOS) as silicon source, TPAOH and distilled water. The solution was aged at 80 °C for 210 minutes under vigorous stirring. Ethanol produced from TEOS hydrolysis was evaporated and a clear gel was obtained. Then, different starch quantities dissolved in aqueous solutions were incorporated and further stirred for 30 minutes at the same temperature. The result suspension was hydrothermally treated at 140 °C in a Teflon lined stainless steel autoclave under static conditions. Crystallization time was varied between 96, 48 and 24 hours and the obtained material was washed with distilled water and dried at 110 °C for 24 hours. Finally, the solid were desorbed under N2 flow (20 ml/min) at 500 °C and further calcined at the same temperature for 8 hours in order to remove the carbonized starch and the organic structure directing agent trapped in the crystals. According to the crystallization time, samples were named as MFI-96, MFI-48 and MFI 24, respectively. The obtained samples were characterized by X Ray Diffraction (XRD), BET and Scanning Electron Microscopy to confirm structure, crystallinity and surface area. From XRD patterns high crystallinity and MFI structure were confirmed, indicating the successful crystallization in short time when soluble starch was added in the synthesis gel. Surface areas calculated from BET were similar to that obtained for traditional ZSM-5 (approximately 360 m2 /g). The so far synthesized and characterized materials were tested as catalysts for peanut shells valorization reactions to obtain platform molecules for the fine chemical industry.
Fil: Bonetto, Luciana. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina.
Fil: Renzini, María Soledad. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina.
Fil: Saux, Clara. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina.
Fil: Pierella, Liliana Beatriz. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. - Materia
-
ZSM-5
Synthesis
Starch - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- 2022-05-30T21:38:19Z
- Repositorio
.jpg)
- Institución
- Universidad Tecnológica Nacional
- OAI Identificador
- oai:ria.utn.edu.ar:20.500.12272/6536
Ver los metadatos del registro completo
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ZSM-5 fast synthesis employing soluble starch as templateBonetto, LucianaRenzini, María SoledadSaux, ClaraPierella, Liliana BeatrizZSM-5SynthesisStarchSolid catalysts with a zeolitic framework were synthesized in the ZSM-5 (MFI) topology employing tetrapropyl ammonium hydroxide (TPAOH) as structure directing agent and soluble starch as template in order to be employed in biomass revalorization reactions. It should be noted that starch is a soluble, biodegradable, low cost and nontoxic polymeric carbohydrate obtained from agricultural raw materials. Starch is employed in thissynthesis processfor pores generation and crystal connection to produce a material with MFI morphology type. ZSM-5 is a medium pore material from the pentasil zeolites group. The traditional synthesis procedure [1] takes around 10 days to obtain the MFI structure. In this new procedure, ZSM-5 type material is obtained by a hydrothermal treatment but in a shorter crystallization time. The effect of time on structure and cristallinity was studied. Zeolite synthesis was done employing sodium aluminate (NaAlO2) as aluminum source, tetraethyl orthosilicate (TEOS) as silicon source, TPAOH and distilled water. The solution was aged at 80 °C for 210 minutes under vigorous stirring. Ethanol produced from TEOS hydrolysis was evaporated and a clear gel was obtained. Then, different starch quantities dissolved in aqueous solutions were incorporated and further stirred for 30 minutes at the same temperature. The result suspension was hydrothermally treated at 140 °C in a Teflon lined stainless steel autoclave under static conditions. Crystallization time was varied between 96, 48 and 24 hours and the obtained material was washed with distilled water and dried at 110 °C for 24 hours. Finally, the solid were desorbed under N2 flow (20 ml/min) at 500 °C and further calcined at the same temperature for 8 hours in order to remove the carbonized starch and the organic structure directing agent trapped in the crystals. According to the crystallization time, samples were named as MFI-96, MFI-48 and MFI 24, respectively. The obtained samples were characterized by X Ray Diffraction (XRD), BET and Scanning Electron Microscopy to confirm structure, crystallinity and surface area. From XRD patterns high crystallinity and MFI structure were confirmed, indicating the successful crystallization in short time when soluble starch was added in the synthesis gel. Surface areas calculated from BET were similar to that obtained for traditional ZSM-5 (approximately 360 m2 /g). The so far synthesized and characterized materials were tested as catalysts for peanut shells valorization reactions to obtain platform molecules for the fine chemical industry.Fil: Bonetto, Luciana. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina.Fil: Renzini, María Soledad. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina.Fil: Saux, Clara. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina.Fil: Pierella, Liliana Beatriz. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina.2022-05-30T21:38:19Z2022-05-30T21:38:19Z2017info:eu-repo/semantics/conferenceObjectinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciapdfapplication/pdf2° Bioeconomy Congress (2017).http://hdl.handle.net/20.500.12272/6536enginfo:eu-repo/semantics/openAccess2022-05-30T21:38:19Zhttp://creativecommons.org/licenses/by-nc-nd/4.0/Attribution-NonCommercial-NoDerivatives 4.0 InternacionalPierella, Liliana BeatrizNo comercial. Sólo de uso académico.reponame:Repositorio Institucional Abierto (UTN)instname:Universidad Tecnológica Nacional2026-10-01T11:59:23Zoai:ria.utn.edu.ar:20.500.12272/6536instacron:UTNInstitucionalhttp://ria.utn.edu.ar/Universidad públicaNo correspondehttp://ria.utn.edu.ar/oaigestionria@rec.utn.edu.ar; fsuarez@rec.utn.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:a2026-10-01 11:59:23.824Repositorio Institucional Abierto (UTN) - Universidad Tecnológica Nacionalfalse |
| dc.title.none.fl_str_mv |
ZSM-5 fast synthesis employing soluble starch as template |
| title |
ZSM-5 fast synthesis employing soluble starch as template |
| spellingShingle |
ZSM-5 fast synthesis employing soluble starch as template Bonetto, Luciana ZSM-5 Synthesis Starch |
| title_short |
ZSM-5 fast synthesis employing soluble starch as template |
| title_full |
ZSM-5 fast synthesis employing soluble starch as template |
| title_fullStr |
ZSM-5 fast synthesis employing soluble starch as template |
| title_full_unstemmed |
ZSM-5 fast synthesis employing soluble starch as template |
| title_sort |
ZSM-5 fast synthesis employing soluble starch as template |
| dc.creator.none.fl_str_mv |
Bonetto, Luciana Renzini, María Soledad Saux, Clara Pierella, Liliana Beatriz |
| author |
Bonetto, Luciana |
| author_facet |
Bonetto, Luciana Renzini, María Soledad Saux, Clara Pierella, Liliana Beatriz |
| author_role |
author |
| author2 |
Renzini, María Soledad Saux, Clara Pierella, Liliana Beatriz |
| author2_role |
author author author |
| dc.subject.none.fl_str_mv |
ZSM-5 Synthesis Starch |
| topic |
ZSM-5 Synthesis Starch |
| dc.description.none.fl_txt_mv |
Solid catalysts with a zeolitic framework were synthesized in the ZSM-5 (MFI) topology employing tetrapropyl ammonium hydroxide (TPAOH) as structure directing agent and soluble starch as template in order to be employed in biomass revalorization reactions. It should be noted that starch is a soluble, biodegradable, low cost and nontoxic polymeric carbohydrate obtained from agricultural raw materials. Starch is employed in thissynthesis processfor pores generation and crystal connection to produce a material with MFI morphology type. ZSM-5 is a medium pore material from the pentasil zeolites group. The traditional synthesis procedure [1] takes around 10 days to obtain the MFI structure. In this new procedure, ZSM-5 type material is obtained by a hydrothermal treatment but in a shorter crystallization time. The effect of time on structure and cristallinity was studied. Zeolite synthesis was done employing sodium aluminate (NaAlO2) as aluminum source, tetraethyl orthosilicate (TEOS) as silicon source, TPAOH and distilled water. The solution was aged at 80 °C for 210 minutes under vigorous stirring. Ethanol produced from TEOS hydrolysis was evaporated and a clear gel was obtained. Then, different starch quantities dissolved in aqueous solutions were incorporated and further stirred for 30 minutes at the same temperature. The result suspension was hydrothermally treated at 140 °C in a Teflon lined stainless steel autoclave under static conditions. Crystallization time was varied between 96, 48 and 24 hours and the obtained material was washed with distilled water and dried at 110 °C for 24 hours. Finally, the solid were desorbed under N2 flow (20 ml/min) at 500 °C and further calcined at the same temperature for 8 hours in order to remove the carbonized starch and the organic structure directing agent trapped in the crystals. According to the crystallization time, samples were named as MFI-96, MFI-48 and MFI 24, respectively. The obtained samples were characterized by X Ray Diffraction (XRD), BET and Scanning Electron Microscopy to confirm structure, crystallinity and surface area. From XRD patterns high crystallinity and MFI structure were confirmed, indicating the successful crystallization in short time when soluble starch was added in the synthesis gel. Surface areas calculated from BET were similar to that obtained for traditional ZSM-5 (approximately 360 m2 /g). The so far synthesized and characterized materials were tested as catalysts for peanut shells valorization reactions to obtain platform molecules for the fine chemical industry. Fil: Bonetto, Luciana. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Fil: Renzini, María Soledad. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Fil: Saux, Clara. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Fil: Pierella, Liliana Beatriz. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. |
| description |
Solid catalysts with a zeolitic framework were synthesized in the ZSM-5 (MFI) topology employing tetrapropyl ammonium hydroxide (TPAOH) as structure directing agent and soluble starch as template in order to be employed in biomass revalorization reactions. It should be noted that starch is a soluble, biodegradable, low cost and nontoxic polymeric carbohydrate obtained from agricultural raw materials. Starch is employed in thissynthesis processfor pores generation and crystal connection to produce a material with MFI morphology type. ZSM-5 is a medium pore material from the pentasil zeolites group. The traditional synthesis procedure [1] takes around 10 days to obtain the MFI structure. In this new procedure, ZSM-5 type material is obtained by a hydrothermal treatment but in a shorter crystallization time. The effect of time on structure and cristallinity was studied. Zeolite synthesis was done employing sodium aluminate (NaAlO2) as aluminum source, tetraethyl orthosilicate (TEOS) as silicon source, TPAOH and distilled water. The solution was aged at 80 °C for 210 minutes under vigorous stirring. Ethanol produced from TEOS hydrolysis was evaporated and a clear gel was obtained. Then, different starch quantities dissolved in aqueous solutions were incorporated and further stirred for 30 minutes at the same temperature. The result suspension was hydrothermally treated at 140 °C in a Teflon lined stainless steel autoclave under static conditions. Crystallization time was varied between 96, 48 and 24 hours and the obtained material was washed with distilled water and dried at 110 °C for 24 hours. Finally, the solid were desorbed under N2 flow (20 ml/min) at 500 °C and further calcined at the same temperature for 8 hours in order to remove the carbonized starch and the organic structure directing agent trapped in the crystals. According to the crystallization time, samples were named as MFI-96, MFI-48 and MFI 24, respectively. The obtained samples were characterized by X Ray Diffraction (XRD), BET and Scanning Electron Microscopy to confirm structure, crystallinity and surface area. From XRD patterns high crystallinity and MFI structure were confirmed, indicating the successful crystallization in short time when soluble starch was added in the synthesis gel. Surface areas calculated from BET were similar to that obtained for traditional ZSM-5 (approximately 360 m2 /g). The so far synthesized and characterized materials were tested as catalysts for peanut shells valorization reactions to obtain platform molecules for the fine chemical industry. |
| publishDate |
2017 |
| dc.date.none.fl_str_mv |
2017 2022-05-30T21:38:19Z 2022-05-30T21:38:19Z |
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info:eu-repo/semantics/conferenceObject info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_5794 info:ar-repo/semantics/documentoDeConferencia |
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conferenceObject |
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publishedVersion |
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2° Bioeconomy Congress (2017). http://hdl.handle.net/20.500.12272/6536 |
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2° Bioeconomy Congress (2017). |
| url |
http://hdl.handle.net/20.500.12272/6536 |
| dc.language.none.fl_str_mv |
eng |
| language |
eng |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess 2022-05-30T21:38:19Z http://creativecommons.org/licenses/by-nc-nd/4.0/ Attribution-NonCommercial-NoDerivatives 4.0 Internacional Pierella, Liliana Beatriz No comercial. Sólo de uso académico. |
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openAccess |
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2022-05-30T21:38:19Z http://creativecommons.org/licenses/by-nc-nd/4.0/ Attribution-NonCommercial-NoDerivatives 4.0 Internacional Pierella, Liliana Beatriz No comercial. Sólo de uso académico. |
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