Lanthanum oxide-promoted cobalt catalyst supported on mesoporous alumina for syngas production via methane dry reforming / (Record no. 97599)

MARC details
000 -LEADER
fixed length control field 04351ntm a2200349 i 4500
003 - CONTROL NUMBER IDENTIFIER
control field MY-KuUP
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20251125110111.0
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007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
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fixed length control field 220912t20222022my a|||fr|||| 000 0 eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number THE0009420 (Local)
Qualifying information hardback
040 ## - CATALOGING SOURCE
Original cataloging agency UMP
Language of cataloging eng
Transcribing agency UMP
Description conventions rda
090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN)
Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) KK.T43 2022 r Thesis
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Thang, Tran Ngoc,
Relator term author.
245 10 - TITLE STATEMENT
Title Lanthanum oxide-promoted cobalt catalyst supported on mesoporous alumina for syngas production via methane dry reforming /
Statement of responsibility, etc. Tran Ngoc Thang
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture Pahang:
Name of producer, publisher, distributor, manufacturer UMP,
Date of production, publication, distribution, manufacture, or copyright notice 2022
264 #4 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice © 2022
300 ## - PHYSICAL DESCRIPTION
Extent xv, 152 pages :
Other physical details Illustration ;
Dimensions 30 cm. +
Accompanying material 1 CD-ROM
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Content type term text
Source rdacontent
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Content type term text
Source rdacontent
337 ## - MEDIA TYPE
Media type term unmediated
Source rdamedia
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Media type term computer
Source rdamedia
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Carrier type term volume
Source rdacarrier
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Carrier type term computer disc
Source rdacarrier
347 ## - DIGITAL FILE CHARACTERISTICS
File type text file
Encoding format PDF
Source rda
500 ## - GENERAL NOTE
General note College of Engineering
502 ## - DISSERTATION NOTE
Dissertation note Thesis (Doctor of Philosophy) -- Universiti Malaysia Pahang – 2022
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note Includes bibliographical reference
520 3# - SUMMARY, ETC.
Summary, etc. Methane dry reforming reaction (MDR) has recently emerged as a promising multipurpose approach for converting two greenhouse gasses, included carbon dioxide (CO2) and methane (CH4), into valuable feedstock for downstream petrochemical processes. At present, there is still a challenge in developing the highly stable and active catalysts for MDR reaction as well as better resistance to carbon deposition. Though the mesoporous alumina supported Co-based catalysts have recently appeared to be the potential catalysts. However, the common starting materials for preparing these wellordered mesoporous catalyst supports are organic precursors and anhydrous ethanol which are quite expensive and harmful to the environment. Therefore, in this study, mesoporous alumina (Al2O3), fabricated using a cheap and available inorganic aluminium precursor in binary water-ethanol solvent, was implemented as support for cobalt catalyst. This investigation aimed to design an effective cobalt-based catalyst system for MDR reaction, which overcomes coke-related deactivation barriers. The promotional effect of La2O3 on the physicochemical features of Al2O3 supported cobalt catalyst and its catalytic performance were also elucidated. The catalyst evaluations in MDR reaction were conducted for 10%Co/Al2O3 and La2O3-promoted 10%Co/Al2O3 catalysts (La loading was in 1% – 8%) in a fixed-bed reactor at temperature range of 923 – 1073 K and partial pressure of individual reactant from 10 to 40 kPa. The Al2O3 support has BET surface area of 173.4 m2 g-1 and cobalt nanoparticles were finely dispersed on the support with desired crystallite size ranged from 5.2 - 9.2 nm. The strong interaction of CoO and Al2O3 phases was confirmed by the presence of cobalt-aluminate spinel and the textural structure of catalysts was stable with reaction temperature. The promotion behavior of La2O3 facilitated H2-reduction by providing higher electron density and enhanced oxygen vacancy in 10%Co/Al2O3. The addition of La2O3 could reduce the apparent activation energy of CH4 consumption; hence, increasing CH4 conversion up to 93.7% at 1073 K. Lanthanum dioxycarbonate transitional phase formed in situ during MDR was accountable for mitigating deposited carbon via redox cycle for 17-30% relying on reaction temperature. Additionally, the oxygen vacancy degree increased to 73.3% with La2O3 promotion. 5%La loading was an optimal promoter content for reactant conversions as well as yield of H2 and CO. 5%La-10%Co/Al2O3 also exhibited the highest resistance to carbon deposition owing to the basic nature, redox feature of La2O3 dopant. The MDR reaction over 5%La-10%Co/Al2O3 catalyst was convinced to follow an associative adsorption mode of CH4 and CO2 on dual or different sites of active particles and the catalyst exhibited a good stability during 48 h reaction at 1023 K. The resulting H2/CO ratios of 0.84-0.98 are suitable for Fischer-Tropsch reaction in downstream to generate liquid hydrocarbon fuels. As a result, the employment of mesoporous alumina support and La2O3 promoter efficiently boosted the Co activity in MDR reaction along with suppressing the carbon deposition on the catalyst surface.
610 20 - SUBJECT ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element College of Engineering
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Library of Congress Classification
Koha item type Thesis
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Collection Home library Current library Date acquired Total checkouts Full call number Barcode Date last seen Copy number Price effective from Koha item type
  Not lost Library of Congress Classification   Not for loan Reference UMPLIB GAMBANG UMPLIB GAMBANG 12/09/2022   KK.T43 2022 r Thesis T000001884 12/09/2022 1 12/09/2022 Thesis
  Not lost Library of Congress Classification   Not for loan Reference UMPLIB GAMBANG UMPLIB GAMBANG 12/09/2022   CD13106 T000001885 30/01/2023 1 12/09/2022 Thesis

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