Novel silica hybrid xerogels prepared by co-condensation of TEOS and ClPhTEOS: a chemical and morphological study

dc.contributor.authorCruz Quesada, Guillermo
dc.contributor.authorEspinal Viguri, Maialen
dc.contributor.authorLópez Ramón, María Victoria
dc.contributor.authorGarrido Segovia, Julián José
dc.contributor.departmentCienciases_ES
dc.contributor.departmentZientziakeu
dc.contributor.departmentInstitute for Advanced Materials and Mathematics - INAMAT2en
dc.date.accessioned2023-04-12T17:19:59Z
dc.date.available2023-04-12T17:19:59Z
dc.date.issued2022
dc.date.updated2023-04-12T17:19:59Z
dc.description.abstractThe search for new materials with improved properties for advanced applications is, nowadays, one of the most relevant and booming fields for scientists due to the environmental and technological needs of our society. Within this demand, hybrid siliceous materials, made out of organic and inorganic species (ORMOSILs), have emerged as an alternative with endless chemical and textural possibilities by incorporating in their structure the properties of inorganic compounds (i.e., mechanical, thermal, and structural stability) in synergy with those of organic compounds (functionality and flexibility), and thus, bestowing the material with unique properties, which allow access to multiple applications. In this work, synthesis using the sol-gel method of a series of new hybrid materials prepared by the co-condensation of tetraethoxysilane (TEOS) and 4-chlorophenyltriethoxysilane (ClPhTEOS) in different molar ratios is described. The aim of the study is not only the preparation of new materials but also their characterization by means of different techniques (FT-IR, 29Si NMR, X-ray Diffraction, and N2/CO2 adsorption, among others) to obtain information on their chemical behavior and porous structure. Understanding how the chemical and textural properties of these materials are modulated with respect to the molar percentage of organic precursor will help to envisage their possible applications: From the most conventional such as catalysis, adsorption, or separation, to the most advanced in nanotechnology such as microelectronics, photoluminescence, non-linear optics, or sensorics.en
dc.description.sponsorshipThis research was funded by “Ministerio de Ciencia e Innovación” (Project ref. PID2020-113558RB-C42).en
dc.format.mimetypeapplication/pdfen
dc.identifier.citationCruz-Quesada, G., Espinal-Viguri, M., López-Ramón, M., & Garrido, J. (2022). Novel silica hybrid xerogels prepared by co-condensation of teos and clphteos: A chemical and morphological study. Gels, 8(10), 677. https://doi.org/10.3390/gels8100677en
dc.identifier.doi10.3390/gels8100677
dc.identifier.issn2310-2861
dc.identifier.urihttps://academica-e.unavarra.es/handle/2454/45113
dc.language.isoengen
dc.publisherMDPIen
dc.relation.ispartofGels 2022, 8(10), 677en
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-113558RB-C42/ES/
dc.relation.publisherversionhttps://doi.org/10.3390/gels8100677
dc.rights© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.en
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectChemical-textural propertiesen
dc.subjectChlorophenyltriethoxysilaneen
dc.subjectHybrid materialsen
dc.subjectOrdered structuresen
dc.subjectORMOSILsen
dc.subjectSilica speciesen
dc.subjectTEOSen
dc.subjectXerogelsen
dc.titleNovel silica hybrid xerogels prepared by co-condensation of TEOS and ClPhTEOS: a chemical and morphological studyen
dc.typeinfo:eu-repo/semantics/article
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dspace.entity.typePublication
relation.isAuthorOfPublication93ef1ad3-369a-4450-a3a4-1705e61480a7
relation.isAuthorOfPublication41646be9-5d5a-4443-8186-1e36f738764b
relation.isAuthorOfPublicationa1dc7e87-ac55-4720-b78e-455e2c300cac
relation.isAuthorOfPublication.latestForDiscovery93ef1ad3-369a-4450-a3a4-1705e61480a7

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