Macro-structured carbon nanofibers catalysts on titania extrudate and cordierite monolith for selective hydrogenation

Jie Zhu

Research output: ThesisPhD Thesis - Research UT, graduation UTAcademic

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Abstract

Macro-structured carbon nanofibers materials on large Titania particles (CNF/TiO2) and cordierite monolith (CNF/TiO2/monolith) were synthesized in this thesis, for the purpose of avoiding or diminishing internal mass transfer limitations in catalysis. Their supported palladium catalysts (Pd/CNF/TiO2 and Pd/CNF/TiO2/monolith) were compared with some catalysts, including palladium catalysts supported on activated carbon (Pd/AC), meso-porous carbon (Pd/MC) and carbon nanofibers (Pd/CNF). Their catalytic properties were evaluated for selective hydrogenation of citral, cinnamaldehyde (CAL) and 4-carboxybenzaldehyde (4-CBA) to determine if as-prepared macro-structured carbon nanofibers catalysts offer advantages in enhancing the activity and the selectivity in these reactions. In catalyst preparation, the synthesized Pd/CNF/TiO2 and Pd/CNF/TiO2/monolith had the good textural and structural properties: the BET surface areas were 60 m2/g and 31 m2/g, respectively; the mesopore structure dominated the pore space of both catalysts, which is beneficial for eliminating mass transfer limitations. As-prepared Pd/CNF/TiO2 was used in selective hydrogenation of citral. Its catalytic property was estimated using Weisz-Prater criterion, and the result was compared to Pd/AC. The calculating results of Weisz-Prater numbers (less than 0.3 of each reactant) inferred the absence of internal diffusion limitations in Pd/CNF/TiO2. It is in accordance with the high citronellal selectivity in citral hydrogenation over it. Meso- and macro-pores, the dominant structures in Pd/CNF/TiO2, resulted in the elimination of internal diffusion limitation in the catalyst. In addition, CNF/TiO2/monolith was employed for two model reactions, selective hydrogenation of CAL and 4-CBA. The effects of mass transfer on catalyst performance were studied experimentally and the results are described using simple kinetic models. The results showed that, catalytic performance of Pd/CNF/TiO2/monolith is similar to Pd/CNF and Pd/AC with particles as small as 50 micron (Pd/AC50), whereas Pd/AC with larger support particles revealed lower activity due to internal mass transfer limitation. Remarkably, the conversion level at which the maximum yield of intermediate product is achieved is highest for Pd/CNF/TiO2/monolith. This advantage is assigned to superior internal mass transfer properties, thanks to high porosity, low tortuosity and short diffusion length of the CNF layer. Clearly, Pd/CNF/TiO2/monolith applied as a fixed bed outperforms slurry catalysts, abandoning the need of a filtration section.
Original languageEnglish
Awarding Institution
  • University of Twente
Supervisors/Advisors
  • Lefferts, Leon, Supervisor
Award date16 Sep 2015
Place of PublicationEnschede
Publisher
Print ISBNs978-90-365-3942-5
DOIs
Publication statusPublished - 16 Sep 2015

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Carbon nanofibers
Hydrogenation
Macros
Catalysts
citral
Mass transfer
Palladium
titanium dioxide
cordierite
Catalyst selectivity
Catalyst supports
Activated carbon
Catalysis
Structural properties

Keywords

  • METIS-311518
  • IR-97087

Cite this

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title = "Macro-structured carbon nanofibers catalysts on titania extrudate and cordierite monolith for selective hydrogenation",
abstract = "Macro-structured carbon nanofibers materials on large Titania particles (CNF/TiO2) and cordierite monolith (CNF/TiO2/monolith) were synthesized in this thesis, for the purpose of avoiding or diminishing internal mass transfer limitations in catalysis. Their supported palladium catalysts (Pd/CNF/TiO2 and Pd/CNF/TiO2/monolith) were compared with some catalysts, including palladium catalysts supported on activated carbon (Pd/AC), meso-porous carbon (Pd/MC) and carbon nanofibers (Pd/CNF). Their catalytic properties were evaluated for selective hydrogenation of citral, cinnamaldehyde (CAL) and 4-carboxybenzaldehyde (4-CBA) to determine if as-prepared macro-structured carbon nanofibers catalysts offer advantages in enhancing the activity and the selectivity in these reactions. In catalyst preparation, the synthesized Pd/CNF/TiO2 and Pd/CNF/TiO2/monolith had the good textural and structural properties: the BET surface areas were 60 m2/g and 31 m2/g, respectively; the mesopore structure dominated the pore space of both catalysts, which is beneficial for eliminating mass transfer limitations. As-prepared Pd/CNF/TiO2 was used in selective hydrogenation of citral. Its catalytic property was estimated using Weisz-Prater criterion, and the result was compared to Pd/AC. The calculating results of Weisz-Prater numbers (less than 0.3 of each reactant) inferred the absence of internal diffusion limitations in Pd/CNF/TiO2. It is in accordance with the high citronellal selectivity in citral hydrogenation over it. Meso- and macro-pores, the dominant structures in Pd/CNF/TiO2, resulted in the elimination of internal diffusion limitation in the catalyst. In addition, CNF/TiO2/monolith was employed for two model reactions, selective hydrogenation of CAL and 4-CBA. The effects of mass transfer on catalyst performance were studied experimentally and the results are described using simple kinetic models. The results showed that, catalytic performance of Pd/CNF/TiO2/monolith is similar to Pd/CNF and Pd/AC with particles as small as 50 micron (Pd/AC50), whereas Pd/AC with larger support particles revealed lower activity due to internal mass transfer limitation. Remarkably, the conversion level at which the maximum yield of intermediate product is achieved is highest for Pd/CNF/TiO2/monolith. This advantage is assigned to superior internal mass transfer properties, thanks to high porosity, low tortuosity and short diffusion length of the CNF layer. Clearly, Pd/CNF/TiO2/monolith applied as a fixed bed outperforms slurry catalysts, abandoning the need of a filtration section.",
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Macro-structured carbon nanofibers catalysts on titania extrudate and cordierite monolith for selective hydrogenation. / Zhu, Jie.

Enschede : Universiteit Twente, 2015. 129 p.

Research output: ThesisPhD Thesis - Research UT, graduation UTAcademic

TY - THES

T1 - Macro-structured carbon nanofibers catalysts on titania extrudate and cordierite monolith for selective hydrogenation

AU - Zhu, Jie

PY - 2015/9/16

Y1 - 2015/9/16

N2 - Macro-structured carbon nanofibers materials on large Titania particles (CNF/TiO2) and cordierite monolith (CNF/TiO2/monolith) were synthesized in this thesis, for the purpose of avoiding or diminishing internal mass transfer limitations in catalysis. Their supported palladium catalysts (Pd/CNF/TiO2 and Pd/CNF/TiO2/monolith) were compared with some catalysts, including palladium catalysts supported on activated carbon (Pd/AC), meso-porous carbon (Pd/MC) and carbon nanofibers (Pd/CNF). Their catalytic properties were evaluated for selective hydrogenation of citral, cinnamaldehyde (CAL) and 4-carboxybenzaldehyde (4-CBA) to determine if as-prepared macro-structured carbon nanofibers catalysts offer advantages in enhancing the activity and the selectivity in these reactions. In catalyst preparation, the synthesized Pd/CNF/TiO2 and Pd/CNF/TiO2/monolith had the good textural and structural properties: the BET surface areas were 60 m2/g and 31 m2/g, respectively; the mesopore structure dominated the pore space of both catalysts, which is beneficial for eliminating mass transfer limitations. As-prepared Pd/CNF/TiO2 was used in selective hydrogenation of citral. Its catalytic property was estimated using Weisz-Prater criterion, and the result was compared to Pd/AC. The calculating results of Weisz-Prater numbers (less than 0.3 of each reactant) inferred the absence of internal diffusion limitations in Pd/CNF/TiO2. It is in accordance with the high citronellal selectivity in citral hydrogenation over it. Meso- and macro-pores, the dominant structures in Pd/CNF/TiO2, resulted in the elimination of internal diffusion limitation in the catalyst. In addition, CNF/TiO2/monolith was employed for two model reactions, selective hydrogenation of CAL and 4-CBA. The effects of mass transfer on catalyst performance were studied experimentally and the results are described using simple kinetic models. The results showed that, catalytic performance of Pd/CNF/TiO2/monolith is similar to Pd/CNF and Pd/AC with particles as small as 50 micron (Pd/AC50), whereas Pd/AC with larger support particles revealed lower activity due to internal mass transfer limitation. Remarkably, the conversion level at which the maximum yield of intermediate product is achieved is highest for Pd/CNF/TiO2/monolith. This advantage is assigned to superior internal mass transfer properties, thanks to high porosity, low tortuosity and short diffusion length of the CNF layer. Clearly, Pd/CNF/TiO2/monolith applied as a fixed bed outperforms slurry catalysts, abandoning the need of a filtration section.

AB - Macro-structured carbon nanofibers materials on large Titania particles (CNF/TiO2) and cordierite monolith (CNF/TiO2/monolith) were synthesized in this thesis, for the purpose of avoiding or diminishing internal mass transfer limitations in catalysis. Their supported palladium catalysts (Pd/CNF/TiO2 and Pd/CNF/TiO2/monolith) were compared with some catalysts, including palladium catalysts supported on activated carbon (Pd/AC), meso-porous carbon (Pd/MC) and carbon nanofibers (Pd/CNF). Their catalytic properties were evaluated for selective hydrogenation of citral, cinnamaldehyde (CAL) and 4-carboxybenzaldehyde (4-CBA) to determine if as-prepared macro-structured carbon nanofibers catalysts offer advantages in enhancing the activity and the selectivity in these reactions. In catalyst preparation, the synthesized Pd/CNF/TiO2 and Pd/CNF/TiO2/monolith had the good textural and structural properties: the BET surface areas were 60 m2/g and 31 m2/g, respectively; the mesopore structure dominated the pore space of both catalysts, which is beneficial for eliminating mass transfer limitations. As-prepared Pd/CNF/TiO2 was used in selective hydrogenation of citral. Its catalytic property was estimated using Weisz-Prater criterion, and the result was compared to Pd/AC. The calculating results of Weisz-Prater numbers (less than 0.3 of each reactant) inferred the absence of internal diffusion limitations in Pd/CNF/TiO2. It is in accordance with the high citronellal selectivity in citral hydrogenation over it. Meso- and macro-pores, the dominant structures in Pd/CNF/TiO2, resulted in the elimination of internal diffusion limitation in the catalyst. In addition, CNF/TiO2/monolith was employed for two model reactions, selective hydrogenation of CAL and 4-CBA. The effects of mass transfer on catalyst performance were studied experimentally and the results are described using simple kinetic models. The results showed that, catalytic performance of Pd/CNF/TiO2/monolith is similar to Pd/CNF and Pd/AC with particles as small as 50 micron (Pd/AC50), whereas Pd/AC with larger support particles revealed lower activity due to internal mass transfer limitation. Remarkably, the conversion level at which the maximum yield of intermediate product is achieved is highest for Pd/CNF/TiO2/monolith. This advantage is assigned to superior internal mass transfer properties, thanks to high porosity, low tortuosity and short diffusion length of the CNF layer. Clearly, Pd/CNF/TiO2/monolith applied as a fixed bed outperforms slurry catalysts, abandoning the need of a filtration section.

KW - METIS-311518

KW - IR-97087

U2 - 10.3990/1.9789036539425

DO - 10.3990/1.9789036539425

M3 - PhD Thesis - Research UT, graduation UT

SN - 978-90-365-3942-5

PB - Universiteit Twente

CY - Enschede

ER -