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One pot menthol synthesis via hydrogenations of citral and citronellal over montmorillonite-supported Pd/Ni-heteropoly acid bifunctional catalysts

Authors
Shah, Abdul KarimMaitlo, GhulamullahShah, Aqeel AhmedChanna, Iftekhar AhmedKandhro, Ghulam AbbasMaitlo, Hubdar AliBhatti, Umair HassanShah, AhmedMemon, Abdul QayoomJatoi, Abdul SattarPark, Yeung Ho
Issue Date
Sep-2019
Publisher
SPRINGER
Keywords
Citral; Citronellal; Isopulegol; Menthol; Bifunctional catalysts
Citation
REACTION KINETICS MECHANISMS AND CATALYSIS, v.128, no.2, pp 917 - 934
Pages
18
Indexed
SCI
SCIE
SCOPUS
Journal Title
REACTION KINETICS MECHANISMS AND CATALYSIS
Volume
128
Number
2
Start Page
917
End Page
934
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/2143
DOI
10.1007/s11144-019-01679-6
ISSN
1878-5190
1878-5204
Abstract
Menthol synthesis is possible through citral and citronellal hydrogenations via following multistage chemical reactions such as hydrogenation and cyclization. This research mainly focuses on a design of selective, active and cost-effective metal-acid (bifunctional) catalysts for menthol production via citral and citronellal hydrogenations. More specifically, Pd and Ni metals were impregnated over acidic support (e.g., hetero-poly acid supported montmorillonite, HPA_MM). The prepared catalysts were characterized by BET, pyridine adsorption and amine titration methods. Some of the most important parameters such as metal type and loading; applied pressure and reaction time have been investigated throughout this work. The obtained results reveals that the 8 wt% Ni-HPA-MM catalyst (Cat-5) has produced 63% menthols (initial reaction rate 0.126 mmol/min) from citral hydrogenation (80 degrees C, 1.0 MPa) within 24 h. Similarly, during lower applied pressure (0.5 MPa), the production of menthol was significantly improved (approximately 98% of menthol, initial reaction rate similar to 0.138 mmol/min) with the application of 8 wt% Ni-HPA-MM catalyst (Cat-5) in citronellal hydrogenation. Higher menthol selectivity was achieved from both reactions (citral and citronellal hydrogenation) which might be due to the presence of strong Lewis and medium Bronsted acid sites.
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COLLEGE OF ENGINEERING SCIENCES > DEPARTMENT OF MATERIALS SCIENCE AND CHEMICAL ENGINEERING > 1. Journal Articles

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