Catalytic functionalities of nano Ru catalysts supported on TiO2–ZrO2 mixed oxide for vapor phase hydrogenolysis of glycerol to propanediols

Vapor phase hydrogenolysis of glycerol was studied over Ru catalysts supported on TiO 2 –ZrO 2 binary oxide. Ru catalysts with various ruthenium loadings from 1.0 to 6.0 wt% were prepared by deposition–precipitation method on the TiO 2 –ZrO 2 mixed oxide support. These catalysts were characterized b...

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Veröffentlicht in:Applied petrochemical research 2016-03, Vol.6 (1), p.73-87
Hauptverfasser: Kumar, Vanama Pavan, Beltramini, Jorge N., Priya, Samudrala Shanthi, Srikanth, Amirineni, Bhanuchander, Ponnala, Chary, Komandur V. R.
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Sprache:eng
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Zusammenfassung:Vapor phase hydrogenolysis of glycerol was studied over Ru catalysts supported on TiO 2 –ZrO 2 binary oxide. Ru catalysts with various ruthenium loadings from 1.0 to 6.0 wt% were prepared by deposition–precipitation method on the TiO 2 –ZrO 2 mixed oxide support. These catalysts were characterized by X-ray diffraction, H 2 temperature-programmed reduction, NH 3 temperature-programmed desorption, transmission electron microscopy, BET surface area, XPS and CO chemisorption measurements. The catalysts exhibited superior performance for the vapor phase hydrogenolysis of glycerol at moderate temperature and atmospheric pressure. The mixed oxide support plays a significant role in improving the catalytic activity for the production of propanediols. The glycerol conversion and the selectivity of various products depend on the catalyst preparation method and also on the Ru content. The influence of acidity of the catalyst and its correlation to the catalytic performance (selectivity and conversion) has been studied. The weak and strong acidic sites of the catalysts measured by NH 3 -TPD play a key role in selective formation of 1,2-propanediol and 1,3-propanediol. XRD, TEM, XPS and CO chemisorption studies revealed that ruthenium was well dispersed on TiO 2 –ZrO 2 which further contributed to the superior catalytic activity for glycerol hydrogenolysis.
ISSN:2190-5525
2190-5525
2190-5533
DOI:10.1007/s13203-015-0136-8