CYCLISATION-ACETYLATION KINETIC OF (<i>R</i>)-(+)-CITRONELLAL BY Zn<sup>2+</sup>–NATURAL ZEOLITE AS SOLID SOLVENT CATALYST

Kinetic in cyclisation-acetylation of (R)-(+)-citronellal with acetic anhydride was investigated over Zn2+-Natural zeolite (Zn2+-Natzeo) as a catalyst. (R)-(+)-citronellal has been isolated from citronella oil by fractional distillation under reducing pressure. Enantioselective capillary GC on a Sup...

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Main Authors: Edy Cahyono, Muchalal Muchalal, Triyono Triyono, Harno Dwi Pranowo
Format: Article
Language:English
Published: Department of Chemistry, Universitas Gadjah Mada 2010-07-01
Series:Indonesian Journal of Chemistry
Online Access:https://jurnal.ugm.ac.id/ijc/article/view/21459
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author Edy Cahyono
Muchalal Muchalal
Triyono Triyono
Harno Dwi Pranowo
author_facet Edy Cahyono
Muchalal Muchalal
Triyono Triyono
Harno Dwi Pranowo
author_sort Edy Cahyono
collection DOAJ
description Kinetic in cyclisation-acetylation of (R)-(+)-citronellal with acetic anhydride was investigated over Zn2+-Natural zeolite (Zn2+-Natzeo) as a catalyst. (R)-(+)-citronellal has been isolated from citronella oil by fractional distillation under reducing pressure. Enantioselective capillary GC on a Supelco β-DEX 225 column has been used for analysis the enantiomers ratio of citronellal. Catalyst Zn2+-Natzeo has prepared through acid activation of natural zeolite from Malang using HF 1% and HCl 6 M, followed by ion-exchange with 3 M NH4Cl and calcination at 450 °C for 1 h under nitrogen to obtained H-natural zeolite (H-Natzeo). H-Natzeo was modified to Zn2+-Natzeo by ion exchange with 0.1 M ZnCl2. Cyclisation-acetylation reaction was carried out by heating (R)-(+)-citronellal (CIT), acetic anhydride (AA), and 1 g catalyst in glass batch reactor with vigorous stirring at 80 °C. Molar ratio CIT/AA that used, i.e. 0.25; 0.5; 1.0; 1.2 and 1.5. As the reaction proceeded, 1 mL sample was taken off at 10; 20; 30; 60; 120; 180 min and extracted using n-hexane for every molar ratio. Structure analysis of product was conducted by GC-MS. Kinetic of the cyclisation-acetylation reaction was analyzed according to the Langmuir-Hinshelwood mechanism. Increasing molar ratio of CIT/AA will decrease the isopulegyl acetate (IPA) and neo-isopulegyl acetate (NIPA) formation. Rate constant of cyclisation-acetylation reaction catalyzed by Zn2+-Natzeo was 30.964-47.619 mmol(min. g cat)-1 at 80 °C, 30 min and the ratio  adsorption equilibrium constant KCIT/KAA was 7.09.   Keywords: Cyclisation-acetylation, (R)-(+)-citronellal, Zn2+-natural zeolite, kinetic
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spelling doaj.art-862d2a54526346d2bd2363a2883a3bb12022-12-21T20:09:31ZengDepartment of Chemistry, Universitas Gadjah MadaIndonesian Journal of Chemistry1411-94202460-15782010-07-0110218919410.22146/ijc.2145914557CYCLISATION-ACETYLATION KINETIC OF (<i>R</i>)-(+)-CITRONELLAL BY Zn<sup>2+</sup>–NATURAL ZEOLITE AS SOLID SOLVENT CATALYSTEdy Cahyono0Muchalal Muchalal1Triyono Triyono2Harno Dwi Pranowo3Student of Doctorate Program Department of Chemistry, Universitas Gadjah Mada; Department of Chemistry, Universitas Negeri Semarang, Jln. Sekaran, Gunungpati, SemarangDepartment of Chemistry, Universitas Gadjah Mada, Jln. Sekip Utara, YogyakartaDepartment of Chemistry, Universitas Gadjah Mada, Jln. Sekip Utara, YogyakartaDepartment of Chemistry, Universitas Gadjah Mada, Jln. Sekip Utara, YogyakartaKinetic in cyclisation-acetylation of (R)-(+)-citronellal with acetic anhydride was investigated over Zn2+-Natural zeolite (Zn2+-Natzeo) as a catalyst. (R)-(+)-citronellal has been isolated from citronella oil by fractional distillation under reducing pressure. Enantioselective capillary GC on a Supelco β-DEX 225 column has been used for analysis the enantiomers ratio of citronellal. Catalyst Zn2+-Natzeo has prepared through acid activation of natural zeolite from Malang using HF 1% and HCl 6 M, followed by ion-exchange with 3 M NH4Cl and calcination at 450 °C for 1 h under nitrogen to obtained H-natural zeolite (H-Natzeo). H-Natzeo was modified to Zn2+-Natzeo by ion exchange with 0.1 M ZnCl2. Cyclisation-acetylation reaction was carried out by heating (R)-(+)-citronellal (CIT), acetic anhydride (AA), and 1 g catalyst in glass batch reactor with vigorous stirring at 80 °C. Molar ratio CIT/AA that used, i.e. 0.25; 0.5; 1.0; 1.2 and 1.5. As the reaction proceeded, 1 mL sample was taken off at 10; 20; 30; 60; 120; 180 min and extracted using n-hexane for every molar ratio. Structure analysis of product was conducted by GC-MS. Kinetic of the cyclisation-acetylation reaction was analyzed according to the Langmuir-Hinshelwood mechanism. Increasing molar ratio of CIT/AA will decrease the isopulegyl acetate (IPA) and neo-isopulegyl acetate (NIPA) formation. Rate constant of cyclisation-acetylation reaction catalyzed by Zn2+-Natzeo was 30.964-47.619 mmol(min. g cat)-1 at 80 °C, 30 min and the ratio  adsorption equilibrium constant KCIT/KAA was 7.09.   Keywords: Cyclisation-acetylation, (R)-(+)-citronellal, Zn2+-natural zeolite, kinetichttps://jurnal.ugm.ac.id/ijc/article/view/21459
spellingShingle Edy Cahyono
Muchalal Muchalal
Triyono Triyono
Harno Dwi Pranowo
CYCLISATION-ACETYLATION KINETIC OF (<i>R</i>)-(+)-CITRONELLAL BY Zn<sup>2+</sup>–NATURAL ZEOLITE AS SOLID SOLVENT CATALYST
Indonesian Journal of Chemistry
title CYCLISATION-ACETYLATION KINETIC OF (<i>R</i>)-(+)-CITRONELLAL BY Zn<sup>2+</sup>–NATURAL ZEOLITE AS SOLID SOLVENT CATALYST
title_full CYCLISATION-ACETYLATION KINETIC OF (<i>R</i>)-(+)-CITRONELLAL BY Zn<sup>2+</sup>–NATURAL ZEOLITE AS SOLID SOLVENT CATALYST
title_fullStr CYCLISATION-ACETYLATION KINETIC OF (<i>R</i>)-(+)-CITRONELLAL BY Zn<sup>2+</sup>–NATURAL ZEOLITE AS SOLID SOLVENT CATALYST
title_full_unstemmed CYCLISATION-ACETYLATION KINETIC OF (<i>R</i>)-(+)-CITRONELLAL BY Zn<sup>2+</sup>–NATURAL ZEOLITE AS SOLID SOLVENT CATALYST
title_short CYCLISATION-ACETYLATION KINETIC OF (<i>R</i>)-(+)-CITRONELLAL BY Zn<sup>2+</sup>–NATURAL ZEOLITE AS SOLID SOLVENT CATALYST
title_sort cyclisation acetylation kinetic of i r i citronellal by zn sup 2 sup natural zeolite as solid solvent catalyst
url https://jurnal.ugm.ac.id/ijc/article/view/21459
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AT muchalalmuchalal cyclisationacetylationkineticofiricitronellalbyznsup2supnaturalzeoliteassolidsolventcatalyst
AT triyonotriyono cyclisationacetylationkineticofiricitronellalbyznsup2supnaturalzeoliteassolidsolventcatalyst
AT harnodwipranowo cyclisationacetylationkineticofiricitronellalbyznsup2supnaturalzeoliteassolidsolventcatalyst