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Non-mercury catalytic acetylene hydrochlorination over spherical activated-carbon-supported Au–Co(III)–Cu(II) catalysts
[Display omitted] •Ternary Au1Co(III)3Cu1/SAC shows high activity for acetylene hydrochlorination.•A synergic effect of Co(III) and Cu(II) augments the amount of Aun+.•Co(III) inhibits the reduction of Aun+ for its standard electrode potential.•Cu(II) further stabilizes the Au3+ through the way of e...
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Published in: | Journal of catalysis 2014-07, Vol.316, p.141-148 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Ternary Au1Co(III)3Cu1/SAC shows high activity for acetylene hydrochlorination.•A synergic effect of Co(III) and Cu(II) augments the amount of Aun+.•Co(III) inhibits the reduction of Aun+ for its standard electrode potential.•Cu(II) further stabilizes the Au3+ through the way of electron transfer.•The estimated life of the ternary catalyst is greater than 6513h.
Several Au-based catalysts, including catalysts containing Au, Au–Co(III), Au–Cu(II), and Au–Co(III)–Cu(II), were prepared and assessed for their ability to promote acetylene hydrochlorination. The catalysts were characterized by temperature-programmed reduction, temperature-programmed desorption, low-temperature N2 adsorption/desorption, thermogravimetric analysis, X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy. The synergistic effects of Co(III) and Cu(II) enhanced the adsorption of hydrogen chloride over the catalysts and increased the amount of the active species Au+ and Au3+ in the ternary Au1Co(III)3Cu(II)1 catalyst supported on spherical activated carbon. The catalyst attained 99.7% acetylene conversion, 99.9% selectivity to vinyl chloride, and an estimated lifetime exceeding 6513h. These results suggest that the ternary catalyst has potential industrial applications. |
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ISSN: | 0021-9517 1090-2694 |
DOI: | 10.1016/j.jcat.2014.05.005 |