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020 ▼a 9781088365052
035 ▼a (MiAaPQ)AAI13898839
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 247004
0820 ▼a 333
1001 ▼a Wang, Cong.
24510 ▼a Selective Conversion of Biomass Model Compounds Using Promoted Metal Catalysts.
260 ▼a [S.l.]: ▼b University of Pennsylvania., ▼c 2019.
260 1 ▼a Ann Arbor: ▼b ProQuest Dissertations & Theses, ▼c 2019.
300 ▼a 226 p.
500 ▼a Source: Dissertations Abstracts International, Volume: 81-05, Section: B.
500 ▼a Advisor: Gorte, Raymond J.
5021 ▼a Thesis (Ph.D.)--University of Pennsylvania, 2019.
506 ▼a This item must not be sold to any third party vendors.
520 ▼a Extensive research and development have gone into modern biomass upgrading in order to mitigate the environmental concerns and other impending challenges associated with conventional fuels and chemicals. The phenolic and furanic compounds produced by primary upgrading processes represent a collection of biomass intermediates that still preserve the valuable chemical structures, but they require further upgrading due to unfavorable oxygen contents and unstable functional groups. This dissertation seeks to demonstrate the viability of utilizing bimetallic and metal-oxide-promoted metal catalysts to further upgrade biomass-derived oxygenates by selective C-O bond scissions. Useful fuels and chemicals are produced from model compounds (2-hydroxymethylfurfural, furfural, tetrahydrofurfuryl alcohol and m-cresol) which represent the main fractions of lignocellulosic biomass. In all studies featured in this thesis, promoted metal catalysts exhibit special activity, selectivity and stability to produce desired products, even though the individual components are not active, selective or stable. In order to bridge the gap between these enhanced catalytic performances and their mechanistic fundamentals, well-defined catalysts synthesized by either solvothermal method (for bimetallic nanocrystals) or atomic layer deposition (for metal-oxide-promoted metal catalysts) were also used to characterize the structure-activity relationships. Notably, I will demonstrate in this dissertation that the active form of the Pt-WOx catalyst exists as a thin, submonolayer film of the oxide on the Pt surface. Direct bonding between the Pt and supported WOx complexes both stabilizes the oxide and lowers the barrier to oxygen vacancy formation. The latter plays a pivotal role in the formation of redox sites on the WOx which are active for direct C-O bond hydrogenolysis. These contributions from the fundamentals should help developing catalysts that are suitable for practical applications.
590 ▼a School code: 0175.
650 4 ▼a Chemical engineering.
650 4 ▼a Materials science.
650 4 ▼a Alternative energy.
690 ▼a 0542
690 ▼a 0794
690 ▼a 0363
71020 ▼a University of Pennsylvania. ▼b Chemical and Biomolecular Engineering.
7730 ▼t Dissertations Abstracts International ▼g 81-05B.
773 ▼t Dissertation Abstract International
790 ▼a 0175
791 ▼a Ph.D.
792 ▼a 2019
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T15491984 ▼n KERIS ▼z 이 자료의 원문은 한국교육학술정보원에서 제공합니다.
980 ▼a 202002 ▼f 2020
990 ▼a ***1008102
991 ▼a E-BOOK