Back to results
Bibliographic record · Consultation and access
Artículo

Nature of the active sites in Al-MCM-41 nano-structured catalysts for the selective rearrangement of cyclohexanone oxime toward ɛ-caprolactam

Vaschetto, Eliana Gabriela et al · Elsevier Science · 2014

Open-access full text
Quick overview. Review the resource’s basic details, then access the content using the main button. This page shows only the information needed to identify, cite, and open the work.

Resource access

Open the content from the main option or choose another available source.

CONICET Digital CONICET Digital OAI-PMH
Entrar por CONICET Digital
Main access

Open-access full text

Texto completo identificado como acceso abierto.
Open text

Summary

Descripción general del contenido del recurso.

Al-MCM-41 type nano-structured catalysts with different Al contents were prepared by direct hydrothermal synthesis. All the materials were characterized by XRD, N2 adsorption, TEM, SEM, ICP-OES, FT-IR and adsorption of pyridine coupled to FT-IR spectroscopy. The relationship between the Al contents in the synthesis gel and final solid, the degree of Al introduction in tetrahedral coordination into the framework, the formation of nest silanols and the relative density of the acidic hydroxyl sites has been exhaustively analyzed. We could corroborate that hydroxyl groups present in silanol nests are the direct responsible of the weakly acid character of our materials. Moreover, a critical concentration of framework Al seems to be necessary to generate such nests, after which the acid sites density is strongly increased, according the framework Al amount increasing. The enhancement in the density of acidic nest silanols (active sites for the selective rearrangement of cyclohexanone oxime toward ɛ-caprolactam) reached by increasing the Al content, permitted to us achieve a cyclohexanone oxime conversion about 66%. The ɛ-caprolactam selectivity was 100% for all the evaluated catalysts, indicating that the acidic strength was kept sufficiently weak to not catalyze the formation of by-products. Fil: Vaschetto, Eliana Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigación y Tecnología Química. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química; Argentina Fil: Pecchi Sanchez, Gina Angela. Universidad de Concepción; Chile

How to cite

Elegí el formato que necesitás y copiá la referencia al portapapeles.

APA 7

Vaschetto, E. G. E. A. (2014). Nature of the active sites in Al-MCM-41 nano-structured catalysts for the selective rearrangement of cyclohexanone oxime toward ɛ-caprolactam. http://hdl.handle.net/11336/32027

MLA

Vaschetto, Eliana Gabriela et al. "Nature of the active sites in Al-MCM-41 nano-structured catalysts for the selective rearrangement of cyclohexanone oxime toward ɛ-caprolactam." 2014. http://hdl.handle.net/11336/32027.

Chicago

Vaschetto, Eliana Gabriela et al. 2014. "Nature of the active sites in Al-MCM-41 nano-structured catalysts for the selective rearrangement of cyclohexanone oxime toward ɛ-caprolactam.". http://hdl.handle.net/11336/32027.

Harvard

Vaschetto, E. G. E. A. 2014, Nature of the active sites in Al-MCM-41 nano-structured catalysts for the selective rearrangement of cyclohexanone oxime toward ɛ-caprolactam, Elsevier Science, available at: http://hdl.handle.net/11336/32027 [Accessed 8 Aug. 2026].

Share and print

Save the record, copy its permanent link, or print it as a PDF.

Export reference

You can export the record in common formats for use in a reference manager.

Resource details

Bibliographic information to help confirm that this is the correct material.

Title
Nature of the active sites in Al-MCM-41 nano-structured catalysts for the selective rearrangement of cyclohexanone oxime toward ɛ-caprolactam
Author / contributors
Vaschetto, Eliana Gabriela et al
Publisher
Elsevier Science
Publication year
2014
ISSN
1387-1811
ISSN
1387-1811
Language
English

Subjects

Explore related resources through these subjects.

Copied