Carbazole hydrodenitrogenation over nickel phosphide and Ni-rich bimetallic phosphide catalysts
Highlights • Nickel-based phosphide catalysts out-performed a commercial Ni–Mo catalyst for carbazole HDN. • Nickel phosphide catalysts exhibited excellent stability in a carbazole/benzothiophene feed. • Nickel-based phosphide catalysts favored ring-opened and ring-contracted products. • Ni2P produc...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Bowker, Richard H. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2014 |
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| Schlagwörter: |
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10 |
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| Übergeordnetes Werk: |
Enthalten in: Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity - Bai, Yang ELSEVIER, 2018, an international journal devoted to catalytic science and its applications, Amsterdam [u.a.] |
|---|---|
| Übergeordnetes Werk: |
volume:482 ; year:2014 ; day:22 ; month:07 ; pages:221-230 ; extent:10 |
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| DOI / URN: |
10.1016/j.apcata.2014.05.026 |
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| 520 | |a Highlights • Nickel-based phosphide catalysts out-performed a commercial Ni–Mo catalyst for carbazole HDN. • Nickel phosphide catalysts exhibited excellent stability in a carbazole/benzothiophene feed. • Nickel-based phosphide catalysts favored ring-opened and ring-contracted products. • Ni2P produced more of the partially hydrogenated hydrocarbon cyclohexylbenzene than a Ni–Mo catalyst. | ||
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540 570 |
| title_sort |
carbazole hydrodenitrogenation over nickel phosphide and ni-rich bimetallic phosphide catalysts |
| title_auth |
Carbazole hydrodenitrogenation over nickel phosphide and Ni-rich bimetallic phosphide catalysts |
| abstract |
Highlights • Nickel-based phosphide catalysts out-performed a commercial Ni–Mo catalyst for carbazole HDN. • Nickel phosphide catalysts exhibited excellent stability in a carbazole/benzothiophene feed. • Nickel-based phosphide catalysts favored ring-opened and ring-contracted products. • Ni2P produced more of the partially hydrogenated hydrocarbon cyclohexylbenzene than a Ni–Mo catalyst. |
| abstractGer |
Highlights • Nickel-based phosphide catalysts out-performed a commercial Ni–Mo catalyst for carbazole HDN. • Nickel phosphide catalysts exhibited excellent stability in a carbazole/benzothiophene feed. • Nickel-based phosphide catalysts favored ring-opened and ring-contracted products. • Ni2P produced more of the partially hydrogenated hydrocarbon cyclohexylbenzene than a Ni–Mo catalyst. |
| abstract_unstemmed |
Highlights • Nickel-based phosphide catalysts out-performed a commercial Ni–Mo catalyst for carbazole HDN. • Nickel phosphide catalysts exhibited excellent stability in a carbazole/benzothiophene feed. • Nickel-based phosphide catalysts favored ring-opened and ring-contracted products. • Ni2P produced more of the partially hydrogenated hydrocarbon cyclohexylbenzene than a Ni–Mo catalyst. |
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Carbazole hydrodenitrogenation over nickel phosphide and Ni-rich bimetallic phosphide catalysts |
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https://doi.org/10.1016/j.apcata.2014.05.026 |
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Ilic, Boris Carrillo, Bo A. Reynolds, Michael A. Murray, Brendan D. Bussell, Mark E. |
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