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Potassium Alum [KAl(SO(4))(2)∙12H(2)O] solid catalyst for effective and selective methoxylation production of alpha-pinene ether products

Methoxylation is a relevant technological process applied in the production of high-value α-pinene derivatives. This report investigates the use of potassium alum [KAl(SO(4))(2) · 12H(2)O] as a catalyst in the methoxylation of α-pinene. In this study, the methoxylation reaction was optimized for the...

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Autores principales: Wijayati, Nanik, Lestari, Lulua Romjanah, Wulandari, Lisa Ayuningtyas, Mahatmanti, F. Widhi, Rakainsa, Senda Kartika, Cahyono, Edi, Wahab, Roswanira Abdul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851781/
https://www.ncbi.nlm.nih.gov/pubmed/33553744
http://dx.doi.org/10.1016/j.heliyon.2021.e06058
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author Wijayati, Nanik
Lestari, Lulua Romjanah
Wulandari, Lisa Ayuningtyas
Mahatmanti, F. Widhi
Rakainsa, Senda Kartika
Cahyono, Edi
Wahab, Roswanira Abdul
author_facet Wijayati, Nanik
Lestari, Lulua Romjanah
Wulandari, Lisa Ayuningtyas
Mahatmanti, F. Widhi
Rakainsa, Senda Kartika
Cahyono, Edi
Wahab, Roswanira Abdul
author_sort Wijayati, Nanik
collection PubMed
description Methoxylation is a relevant technological process applied in the production of high-value α-pinene derivatives. This report investigates the use of potassium alum [KAl(SO(4))(2) · 12H(2)O] as a catalyst in the methoxylation of α-pinene. In this study, the methoxylation reaction was optimized for the highest conversion of α-pinene and selectivity, assessed for the factors, catalyst loading (0.5; 1.0; and 1.5 g), volume ratio of α-pinene: methanol (1:4, 1:7, 1:10), reaction temperature (50, 55, 60 and 65 °C), and reaction time (72, 144, 216, 288, 360 min). The highest selectivity of KAl(SO(4))(2)∙12H(2)O in the methoxylation of α-pinene was achieved under an optimal condition of 1 g of catalyst loading, volume ratio of 1:10, as well as the reaction temperature and incubation time of 65 °C and 6 h, respectively. GC–MS results revealed the yields of the methoxylated products from the 98.2% conversion of α-pinene, to be 59.6%, 8.9%, and 7.1% for α-terpinyl methyl ether (TME), fenchyl methyl ether (FME), bornyl methyl ether (BME), respectively. It was apparent that a lower KAl(SO(4))(2)∙12H(2)O loading (0.5–1.5 g) was more economical for the methoxylation reaction. The findings seen here indicated the suitability of the KAl(SO(4))(2) · 12H(2)O to catalyze the methoxylation of α-pinene to produce an commercially important ethers.
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spelling pubmed-78517812021-02-05 Potassium Alum [KAl(SO(4))(2)∙12H(2)O] solid catalyst for effective and selective methoxylation production of alpha-pinene ether products Wijayati, Nanik Lestari, Lulua Romjanah Wulandari, Lisa Ayuningtyas Mahatmanti, F. Widhi Rakainsa, Senda Kartika Cahyono, Edi Wahab, Roswanira Abdul Heliyon Research Article Methoxylation is a relevant technological process applied in the production of high-value α-pinene derivatives. This report investigates the use of potassium alum [KAl(SO(4))(2) · 12H(2)O] as a catalyst in the methoxylation of α-pinene. In this study, the methoxylation reaction was optimized for the highest conversion of α-pinene and selectivity, assessed for the factors, catalyst loading (0.5; 1.0; and 1.5 g), volume ratio of α-pinene: methanol (1:4, 1:7, 1:10), reaction temperature (50, 55, 60 and 65 °C), and reaction time (72, 144, 216, 288, 360 min). The highest selectivity of KAl(SO(4))(2)∙12H(2)O in the methoxylation of α-pinene was achieved under an optimal condition of 1 g of catalyst loading, volume ratio of 1:10, as well as the reaction temperature and incubation time of 65 °C and 6 h, respectively. GC–MS results revealed the yields of the methoxylated products from the 98.2% conversion of α-pinene, to be 59.6%, 8.9%, and 7.1% for α-terpinyl methyl ether (TME), fenchyl methyl ether (FME), bornyl methyl ether (BME), respectively. It was apparent that a lower KAl(SO(4))(2)∙12H(2)O loading (0.5–1.5 g) was more economical for the methoxylation reaction. The findings seen here indicated the suitability of the KAl(SO(4))(2) · 12H(2)O to catalyze the methoxylation of α-pinene to produce an commercially important ethers. Elsevier 2021-01-30 /pmc/articles/PMC7851781/ /pubmed/33553744 http://dx.doi.org/10.1016/j.heliyon.2021.e06058 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Wijayati, Nanik
Lestari, Lulua Romjanah
Wulandari, Lisa Ayuningtyas
Mahatmanti, F. Widhi
Rakainsa, Senda Kartika
Cahyono, Edi
Wahab, Roswanira Abdul
Potassium Alum [KAl(SO(4))(2)∙12H(2)O] solid catalyst for effective and selective methoxylation production of alpha-pinene ether products
title Potassium Alum [KAl(SO(4))(2)∙12H(2)O] solid catalyst for effective and selective methoxylation production of alpha-pinene ether products
title_full Potassium Alum [KAl(SO(4))(2)∙12H(2)O] solid catalyst for effective and selective methoxylation production of alpha-pinene ether products
title_fullStr Potassium Alum [KAl(SO(4))(2)∙12H(2)O] solid catalyst for effective and selective methoxylation production of alpha-pinene ether products
title_full_unstemmed Potassium Alum [KAl(SO(4))(2)∙12H(2)O] solid catalyst for effective and selective methoxylation production of alpha-pinene ether products
title_short Potassium Alum [KAl(SO(4))(2)∙12H(2)O] solid catalyst for effective and selective methoxylation production of alpha-pinene ether products
title_sort potassium alum [kal(so(4))(2)∙12h(2)o] solid catalyst for effective and selective methoxylation production of alpha-pinene ether products
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851781/
https://www.ncbi.nlm.nih.gov/pubmed/33553744
http://dx.doi.org/10.1016/j.heliyon.2021.e06058
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