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Peanut Shell-Derived Carbon Solid Acid with Large Surface Area and Its Application for the Catalytic Hydrolysis of Cyclohexyl Acetate

A carbon solid acid with large surface area (CSALA) was prepared by partial carbonization of H(3)PO(4) pre-treated peanut shells followed by sulfonation with concentrated H(2)SO(4). The structure and acidity of CSALA were characterized by N(2) adsorption–desorption, scanning electron microscopy (SEM...

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Autores principales: Xue, Wei, Sun, Lijun, Yang, Fang, Wang, Zhimiao, Li, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5456599/
https://www.ncbi.nlm.nih.gov/pubmed/28773954
http://dx.doi.org/10.3390/ma9100833
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author Xue, Wei
Sun, Lijun
Yang, Fang
Wang, Zhimiao
Li, Fang
author_facet Xue, Wei
Sun, Lijun
Yang, Fang
Wang, Zhimiao
Li, Fang
author_sort Xue, Wei
collection PubMed
description A carbon solid acid with large surface area (CSALA) was prepared by partial carbonization of H(3)PO(4) pre-treated peanut shells followed by sulfonation with concentrated H(2)SO(4). The structure and acidity of CSALA were characterized by N(2) adsorption–desorption, scanning electron microscopy (SEM), X-ray powder diffraction (XRD), (13)C cross polarization (CP)/magic angle spinning (MAS) nuclear magnetic resonance (NMR), X-ray photoelectron spectroscopy (XPS), Fourier transform-infrared spectroscopy (FT-IR), titration, and elemental analysis. The results demonstrated that the CSALA was an amorphous carbon material with a surface area of 387.4 m(2)/g. SO(3)H groups formed on the surface with a density of 0.46 mmol/g, with 1.11 mmol/g of COOH and 0.39 mmol/g of phenolic OH. Densities of the latter two groups were notably greater than those observed on a carbon solid acid (CSA) with a surface area of 10.1 m(2)/g. The CSALA catalyst showed better performance than the CSA for the hydrolysis of cyclohexyl acetate to cyclohexanol. Under optimal reaction conditions, cyclohexyl acetate conversion was 86.6% with 97.3% selectivity for cyclohexanol, while the results were 25.0% and 99.4%, respectively, catalyzed by CSA. The high activity of the CSALA could be attributed to its high density of COOH and large surface area. Moreover, the CSALA showed good reusability. Its catalytic activity decreased slightly during the first two cycles due to the leaching of polycyclic aromatic hydrocarbon-containing SO(3)H groups, and then remained constant during following uses.
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spelling pubmed-54565992017-07-28 Peanut Shell-Derived Carbon Solid Acid with Large Surface Area and Its Application for the Catalytic Hydrolysis of Cyclohexyl Acetate Xue, Wei Sun, Lijun Yang, Fang Wang, Zhimiao Li, Fang Materials (Basel) Article A carbon solid acid with large surface area (CSALA) was prepared by partial carbonization of H(3)PO(4) pre-treated peanut shells followed by sulfonation with concentrated H(2)SO(4). The structure and acidity of CSALA were characterized by N(2) adsorption–desorption, scanning electron microscopy (SEM), X-ray powder diffraction (XRD), (13)C cross polarization (CP)/magic angle spinning (MAS) nuclear magnetic resonance (NMR), X-ray photoelectron spectroscopy (XPS), Fourier transform-infrared spectroscopy (FT-IR), titration, and elemental analysis. The results demonstrated that the CSALA was an amorphous carbon material with a surface area of 387.4 m(2)/g. SO(3)H groups formed on the surface with a density of 0.46 mmol/g, with 1.11 mmol/g of COOH and 0.39 mmol/g of phenolic OH. Densities of the latter two groups were notably greater than those observed on a carbon solid acid (CSA) with a surface area of 10.1 m(2)/g. The CSALA catalyst showed better performance than the CSA for the hydrolysis of cyclohexyl acetate to cyclohexanol. Under optimal reaction conditions, cyclohexyl acetate conversion was 86.6% with 97.3% selectivity for cyclohexanol, while the results were 25.0% and 99.4%, respectively, catalyzed by CSA. The high activity of the CSALA could be attributed to its high density of COOH and large surface area. Moreover, the CSALA showed good reusability. Its catalytic activity decreased slightly during the first two cycles due to the leaching of polycyclic aromatic hydrocarbon-containing SO(3)H groups, and then remained constant during following uses. MDPI 2016-10-15 /pmc/articles/PMC5456599/ /pubmed/28773954 http://dx.doi.org/10.3390/ma9100833 Text en © 2016 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Xue, Wei
Sun, Lijun
Yang, Fang
Wang, Zhimiao
Li, Fang
Peanut Shell-Derived Carbon Solid Acid with Large Surface Area and Its Application for the Catalytic Hydrolysis of Cyclohexyl Acetate
title Peanut Shell-Derived Carbon Solid Acid with Large Surface Area and Its Application for the Catalytic Hydrolysis of Cyclohexyl Acetate
title_full Peanut Shell-Derived Carbon Solid Acid with Large Surface Area and Its Application for the Catalytic Hydrolysis of Cyclohexyl Acetate
title_fullStr Peanut Shell-Derived Carbon Solid Acid with Large Surface Area and Its Application for the Catalytic Hydrolysis of Cyclohexyl Acetate
title_full_unstemmed Peanut Shell-Derived Carbon Solid Acid with Large Surface Area and Its Application for the Catalytic Hydrolysis of Cyclohexyl Acetate
title_short Peanut Shell-Derived Carbon Solid Acid with Large Surface Area and Its Application for the Catalytic Hydrolysis of Cyclohexyl Acetate
title_sort peanut shell-derived carbon solid acid with large surface area and its application for the catalytic hydrolysis of cyclohexyl acetate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5456599/
https://www.ncbi.nlm.nih.gov/pubmed/28773954
http://dx.doi.org/10.3390/ma9100833
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