CATALYTIC TRANSFER HYDROGENATION OF DUT-52 IN FURFURAL TO FURFURYL ALCOHOL REACTION

Hydrogenation of the carbonyl groups in furfural compounds may produce furfuryl alcohol. Furfuryl alcohol is used in poly(furfurylalcohol) resin and pharmaceutical industries. The hydrogenation process of furfural generally uses high pressure H2. Research related to hydrogenation at a pressure of 1...

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Main Author: Fridayanti Miharja, Martina
Format: Final Project
Language:Indonesia
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Online Access:https://digilib.itb.ac.id/gdl/view/54987
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:54987
spelling id-itb.:549872021-06-11T13:58:33ZCATALYTIC TRANSFER HYDROGENATION OF DUT-52 IN FURFURAL TO FURFURYL ALCOHOL REACTION Fridayanti Miharja, Martina Kimia Indonesia Final Project Furfural, furfuryl alcohol, hydrogenation, Zr-MOFs. INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/54987 Hydrogenation of the carbonyl groups in furfural compounds may produce furfuryl alcohol. Furfuryl alcohol is used in poly(furfurylalcohol) resin and pharmaceutical industries. The hydrogenation process of furfural generally uses high pressure H2. Research related to hydrogenation at a pressure of 1 atm using hydrogen sources other than H2 recently grew as an alternative to a more desirable process. The conversion of furfural to furfuryl alcohol by transfer of the hydrogen alcohol to the carbonyl group is known to be facilitated by Lewis MOF zirconium(IV) acid. Three zirconium MOFs, namely UiO-66, DUT-52 and MOF-808 were used as catalysts and their catalytic performances were observed. As a source of hydrogen, 2-propanol was observed to give better furfural conversion than methanol and ethanol. The reaction yield and furfural conversion were observed by gas chromatography and 1H-NMR (60 MHz). Researcher from UST Korea observed a non-catalytic behavior of DUT-52 when it was employed in the furfural reaction under 2-propanol. As DUT-52 was reportedto have stronger Lewis acidity than UiO-66, the nature of DUT-52 was predicted to have a good catalytic performance in such a reaction. Herein, DUT-52 showed a catalytic activity ofthat was equivalent to that of UiO-66 at 140 °C and 5 h reaction (TOF = 3?5 h?1). This phenomenon was in accordance with the initial hypothesis. The reaction was observed to follow a pseudo 1st reaction order with the highest turn over frequency (TOF) of 6?7 h?1. DUT- 52 was also observed to have a good regeneration potential with a catalyst mass regenerationof 80% and a post-regeneration furfural conversion of 92%. text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
topic Kimia
spellingShingle Kimia
Fridayanti Miharja, Martina
CATALYTIC TRANSFER HYDROGENATION OF DUT-52 IN FURFURAL TO FURFURYL ALCOHOL REACTION
description Hydrogenation of the carbonyl groups in furfural compounds may produce furfuryl alcohol. Furfuryl alcohol is used in poly(furfurylalcohol) resin and pharmaceutical industries. The hydrogenation process of furfural generally uses high pressure H2. Research related to hydrogenation at a pressure of 1 atm using hydrogen sources other than H2 recently grew as an alternative to a more desirable process. The conversion of furfural to furfuryl alcohol by transfer of the hydrogen alcohol to the carbonyl group is known to be facilitated by Lewis MOF zirconium(IV) acid. Three zirconium MOFs, namely UiO-66, DUT-52 and MOF-808 were used as catalysts and their catalytic performances were observed. As a source of hydrogen, 2-propanol was observed to give better furfural conversion than methanol and ethanol. The reaction yield and furfural conversion were observed by gas chromatography and 1H-NMR (60 MHz). Researcher from UST Korea observed a non-catalytic behavior of DUT-52 when it was employed in the furfural reaction under 2-propanol. As DUT-52 was reportedto have stronger Lewis acidity than UiO-66, the nature of DUT-52 was predicted to have a good catalytic performance in such a reaction. Herein, DUT-52 showed a catalytic activity ofthat was equivalent to that of UiO-66 at 140 °C and 5 h reaction (TOF = 3?5 h?1). This phenomenon was in accordance with the initial hypothesis. The reaction was observed to follow a pseudo 1st reaction order with the highest turn over frequency (TOF) of 6?7 h?1. DUT- 52 was also observed to have a good regeneration potential with a catalyst mass regenerationof 80% and a post-regeneration furfural conversion of 92%.
format Final Project
author Fridayanti Miharja, Martina
author_facet Fridayanti Miharja, Martina
author_sort Fridayanti Miharja, Martina
title CATALYTIC TRANSFER HYDROGENATION OF DUT-52 IN FURFURAL TO FURFURYL ALCOHOL REACTION
title_short CATALYTIC TRANSFER HYDROGENATION OF DUT-52 IN FURFURAL TO FURFURYL ALCOHOL REACTION
title_full CATALYTIC TRANSFER HYDROGENATION OF DUT-52 IN FURFURAL TO FURFURYL ALCOHOL REACTION
title_fullStr CATALYTIC TRANSFER HYDROGENATION OF DUT-52 IN FURFURAL TO FURFURYL ALCOHOL REACTION
title_full_unstemmed CATALYTIC TRANSFER HYDROGENATION OF DUT-52 IN FURFURAL TO FURFURYL ALCOHOL REACTION
title_sort catalytic transfer hydrogenation of dut-52 in furfural to furfuryl alcohol reaction
url https://digilib.itb.ac.id/gdl/view/54987
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