Development of bifunctional catalysts synthesized from pyrolyzed and hydrothermalized palm waste for biodiesel production using waste cooking oil

The abundance of waste biomass from palm oil industries creates a new potential for producing activated carbon as catalyst support. The hydrothermal carbonization (HTC) process provides a brilliant alternative to produce activated carbon from biomass samples with higher water content than conv...

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Main Author:	Abdullah, Rose Fadzilah
Format:	Thesis
Language:	English
Published:	2021
Subjects:	Hydrotreating catalysts Oil palm - Waste disposal
Online Access:	http://psasir.upm.edu.my/id/eprint/103801/1/ITMA%202022%2011%20IR.pdf
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id	my-upm-ir.103801
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spelling	my-upm-ir.1038012023-05-05T07:14:55Z Development of bifunctional catalysts synthesized from pyrolyzed and hydrothermalized palm waste for biodiesel production using waste cooking oil 2021-12 Abdullah, Rose Fadzilah The abundance of waste biomass from palm oil industries creates a new potential for producing activated carbon as catalyst support. The hydrothermal carbonization (HTC) process provides a brilliant alternative to produce activated carbon from biomass samples with higher water content than conventional pyrolysis techniques. Therefore, this study aims to produce activated carbon from palm kernel shell (PKS), mesocarp fiber (MF) and empty fruit bunch (EFB) using pyrolysis and HTC techniques. The HTC process favours the breakage of large polymeric molecules in the lignocellulosic material into lower molecular weight organic compounds through hydrolysis, dehydration, decarboxylation, aromatization and recondensation process. Subsequently, the performance of the prepared activated carbon was determined through the application as catalyst support of a bifunctional catalyst. Therefore, the activated carbon was impregnated with K2CO3 and CuO via wet impregnation provided bifunctional characteristics. The state-of-the-art characterization of the synthesized bifunctional catalysts was conducted including N2 adsorption-desorption analysis, functional group determination, surface morphology observation, crystallography study, electron dispersive X-ray mapping, elemental distribution analysis, concentration of basicity and acidity measurement and thermal degradation behaviour analysis. The results show that the HTC technique successfully produced a highly mesoporous activated carbon derived from PKS that had better textural properties than pyrolyzed with a BET surface area of 1411.16 m2 g-1 and 3368.60 m2 g-1, respectively. The produced bifunctional catalyst was applied in the simultaneous esterification and transesterification reaction from the waste cooking oil (WCO) by the conventional reflux system. The high BET surface area provides extra space for active sites impregnation which is very important for producing maximum biodiesel yield from WCO. The catalytic performance results show that the hydrothermalized-activated carbon from PKS (PKSHAC) derived catalyst produced a higher biodiesel yield of 95.3% against 95.0% over the pyrolyzed-activated carbon from PKS (PKSAC) derived catalyst. The activated carbon preparation was continued using MF and EFB, namely hydrothermalized-activated carbon from MF (MFHAC) and EFB (EFBHAC), which exhibited a BET surface area of 3909.33 m2 g-1 and 4056.17 m2 g-1, and produced a maximum biodiesel yield of 96.4% and 97.1%, respectively. The synthesized catalysts sustained up to 5 reaction cycles with more than 80% of biodiesel yield. The carbon structure collapsed due to multiple calcination during the reactivation procedure, and the catalyst poisoning by glyceroxide on the catalyst surface was identified as a deactivation factor. On the other hand, the transformation of biodiesel from WCO was confirmed via proton nuclei magnetic resonance (1H NMR), Fourier transform Infrared (FTIR) and thermal gravimetric analysis (TGA). Fuel properties revealed kinematic viscosity of 3.3 mm2 s-1, the cetane number of 51, the flashpoint of 160.5 °C, cloud and pour point of 11 °C and -3 °C, respectively. Overall, the finding shows the excellent potential of waste materials, especially PKS, MF, and EFB in producing high quality activated carbon as catalyst support via pyrolysis and HTC techniques. The functionalization with K2CO3 and CuO via wet impregnation provides bifunctional that opens the opportunity in utilizing WCO to produce high-quality biodiesel. Hydrotreating catalysts Oil palm - Waste disposal 2021-12 Thesis http://psasir.upm.edu.my/id/eprint/103801/ http://psasir.upm.edu.my/id/eprint/103801/1/ITMA%202022%2011%20IR.pdf text en public doctoral Universiti Putra Malaysia Hydrotreating catalysts Oil palm - Waste disposal Rashid, Umer
institution	Universiti Putra Malaysia
collection	PSAS Institutional Repository
language	English
advisor	Rashid, Umer
topic	Hydrotreating catalysts Oil palm - Waste disposal
spellingShingle	Hydrotreating catalysts Oil palm - Waste disposal Abdullah, Rose Fadzilah Development of bifunctional catalysts synthesized from pyrolyzed and hydrothermalized palm waste for biodiesel production using waste cooking oil
description	The abundance of waste biomass from palm oil industries creates a new potential for producing activated carbon as catalyst support. The hydrothermal carbonization (HTC) process provides a brilliant alternative to produce activated carbon from biomass samples with higher water content than conventional pyrolysis techniques. Therefore, this study aims to produce activated carbon from palm kernel shell (PKS), mesocarp fiber (MF) and empty fruit bunch (EFB) using pyrolysis and HTC techniques. The HTC process favours the breakage of large polymeric molecules in the lignocellulosic material into lower molecular weight organic compounds through hydrolysis, dehydration, decarboxylation, aromatization and recondensation process. Subsequently, the performance of the prepared activated carbon was determined through the application as catalyst support of a bifunctional catalyst. Therefore, the activated carbon was impregnated with K2CO3 and CuO via wet impregnation provided bifunctional characteristics. The state-of-the-art characterization of the synthesized bifunctional catalysts was conducted including N2 adsorption-desorption analysis, functional group determination, surface morphology observation, crystallography study, electron dispersive X-ray mapping, elemental distribution analysis, concentration of basicity and acidity measurement and thermal degradation behaviour analysis. The results show that the HTC technique successfully produced a highly mesoporous activated carbon derived from PKS that had better textural properties than pyrolyzed with a BET surface area of 1411.16 m2 g-1 and 3368.60 m2 g-1, respectively. The produced bifunctional catalyst was applied in the simultaneous esterification and transesterification reaction from the waste cooking oil (WCO) by the conventional reflux system. The high BET surface area provides extra space for active sites impregnation which is very important for producing maximum biodiesel yield from WCO. The catalytic performance results show that the hydrothermalized-activated carbon from PKS (PKSHAC) derived catalyst produced a higher biodiesel yield of 95.3% against 95.0% over the pyrolyzed-activated carbon from PKS (PKSAC) derived catalyst. The activated carbon preparation was continued using MF and EFB, namely hydrothermalized-activated carbon from MF (MFHAC) and EFB (EFBHAC), which exhibited a BET surface area of 3909.33 m2 g-1 and 4056.17 m2 g-1, and produced a maximum biodiesel yield of 96.4% and 97.1%, respectively. The synthesized catalysts sustained up to 5 reaction cycles with more than 80% of biodiesel yield. The carbon structure collapsed due to multiple calcination during the reactivation procedure, and the catalyst poisoning by glyceroxide on the catalyst surface was identified as a deactivation factor. On the other hand, the transformation of biodiesel from WCO was confirmed via proton nuclei magnetic resonance (1H NMR), Fourier transform Infrared (FTIR) and thermal gravimetric analysis (TGA). Fuel properties revealed kinematic viscosity of 3.3 mm2 s-1, the cetane number of 51, the flashpoint of 160.5 °C, cloud and pour point of 11 °C and -3 °C, respectively. Overall, the finding shows the excellent potential of waste materials, especially PKS, MF, and EFB in producing high quality activated carbon as catalyst support via pyrolysis and HTC techniques. The functionalization with K2CO3 and CuO via wet impregnation provides bifunctional that opens the opportunity in utilizing WCO to produce high-quality biodiesel.
format	Thesis
qualification_level	Doctorate
author	Abdullah, Rose Fadzilah
author_facet	Abdullah, Rose Fadzilah
author_sort	Abdullah, Rose Fadzilah
title	Development of bifunctional catalysts synthesized from pyrolyzed and hydrothermalized palm waste for biodiesel production using waste cooking oil
title_short	Development of bifunctional catalysts synthesized from pyrolyzed and hydrothermalized palm waste for biodiesel production using waste cooking oil
title_full	Development of bifunctional catalysts synthesized from pyrolyzed and hydrothermalized palm waste for biodiesel production using waste cooking oil
title_fullStr	Development of bifunctional catalysts synthesized from pyrolyzed and hydrothermalized palm waste for biodiesel production using waste cooking oil
title_full_unstemmed	Development of bifunctional catalysts synthesized from pyrolyzed and hydrothermalized palm waste for biodiesel production using waste cooking oil
title_sort	development of bifunctional catalysts synthesized from pyrolyzed and hydrothermalized palm waste for biodiesel production using waste cooking oil
granting_institution	Universiti Putra Malaysia
publishDate	2021
url	http://psasir.upm.edu.my/id/eprint/103801/1/ITMA%202022%2011%20IR.pdf
_version_	1776100364481724416

Development of bifunctional catalysts synthesized from pyrolyzed and hydrothermalized palm waste for biodiesel production using waste cooking oil

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