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Rational design and synthesis of Pt/...
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Samad, Jadid Ettaz.
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Rational design and synthesis of Pt/silica-alumina metal-acid bifunctional catalysts.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Rational design and synthesis of Pt/silica-alumina metal-acid bifunctional catalysts./
作者:
Samad, Jadid Ettaz.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2016,
面頁冊數:
171 p.
附註:
Source: Dissertation Abstracts International, Volume: 77-12(E), Section: B.
Contained By:
Dissertation Abstracts International77-12B(E).
標題:
Chemical engineering. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10127066
ISBN:
9781339851044
Rational design and synthesis of Pt/silica-alumina metal-acid bifunctional catalysts.
Samad, Jadid Ettaz.
Rational design and synthesis of Pt/silica-alumina metal-acid bifunctional catalysts.
- Ann Arbor : ProQuest Dissertations & Theses, 2016 - 171 p.
Source: Dissertation Abstracts International, Volume: 77-12(E), Section: B.
Thesis (Ph.D.)--University of South Carolina, 2016.
In the domain of rational catalyst design and synthesis, Strong Electrostatic Adsorption (SEA) has been applied with tremendous potential and use. In this study, SEA method has been advanced to thick slurries as well as to mixed oxide systems with a view to synthesizing stable, active and selective catalysts fine-tuned for specific applications.
ISBN: 9781339851044Subjects--Topical Terms:
560457
Chemical engineering.
Rational design and synthesis of Pt/silica-alumina metal-acid bifunctional catalysts.
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In the domain of rational catalyst design and synthesis, Strong Electrostatic Adsorption (SEA) has been applied with tremendous potential and use. In this study, SEA method has been advanced to thick slurries as well as to mixed oxide systems with a view to synthesizing stable, active and selective catalysts fine-tuned for specific applications.
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The main objective was to synthesize metal-acid bifunctional catalysts with controlled ratio and proximity between metal and acid sites in order to analyze their effects on a bifunctional reaction. At first, the difference in charging behavior of silica and alumina in solution was used to selectively deposit Pt onto different domains of silica-alumina mixed oxides (Al-Si). With cationic Pt precursor at neutral to basic pH range, well dispersed Pt/Al-Si catalysts with "atomic scale" intimacy between metal and acid sites were prepared. However, anionic Pt adsorption over Al-Si at low pH resulted in poorly dispersed Pt/Al-Si catalysts with "nanometer scale" intimacy between active sites. In this case it was found that as anionic Pt selectively deposited onto the alumina domains of Al-Si, a critical domain size of alumina was required to stabilize small Pt nanoparticles. These catalysts along with other physically mixed and layered catalysts constituted a series of bifunctional Pt/Al-Si catalysts with varying ratio and proximity between metal and acid sites which were tested in an n-heptane (n-C7) isomerization reaction operating at 350°C and atmospheric pressure.
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From the catalytic results, large (∼20nm) Pt particles over acidic silica-alumina catalysts with "nanometer-scale" proximity displayed a higher degree of bifunctionality than small Pt particles (∼2nm) with "atomic-scale" intimacy. Even more significant is the ratio of acid sites to metal sites. For optimum bifunctional reactivity for n-C 7 isomerization, Pt and amorphous Al-Si based catalysts should be synthesized with a high enough ratio of acid-to-metal sites (>10 acid sites per metal site) and an intermediate degree of intimacy (not atomic-scale but nano- or micrometer-scale) between these two active sites.
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