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Platinum supported on h-mordenite: a highly efficient catalyst for selective hydrogenolysis of glycerol to 1,3-propanediol

journal contribution
posted on 2024-11-02, 00:32 authored by Santhi Priya Samudrala, Ponnala Bhanuchander, Vanama Kumar, Deepa Dumbre, Selvakannan PeriasamySelvakannan Periasamy, Suresh BhargavaSuresh Bhargava, Mannepalli Kantam, Komandur Chary
The selective production of 1,3-propanediol from glycerol under mild reaction conditions is of high interest. The current work describes the use of a highly selective catalyst consisting of platinum supported on mordenite zeolite employed for the first time for vapor phase hydrogenolysis of glycerol to 1,3-propanediol under atmospheric pressure. The catalysts with varying Pt content (0.5-3 wt %) were prepared and thoroughly characterized by X-ray diffraction, temperature-programmed desorption of ammonia, FT-IR of adsorbed pyridine, CO chemisorptions, transmission electron microscopy, X-ray photoelectron spectroscopy, and BET surface area. The influence of reaction parameters has been studied to unveil the optimized reaction conditions. A high 1,3-propanediol selectivity (48.6%) was obtained over a 2 wt % Pt/H-mordenite catalyst at 94.9% glycerol conversion. According to the results obtained, the selectivity to 1,3-propanediol is better influenced by Pt dispersion and Bronsted acidity of the support. A plausible reaction mechanism has been presented. The spent catalyst exhibited consistent activity and selectivity toward the desired product during the glycerol hydrogenolysis reaction.

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Related Materials

  1. 1.
    DOI - Is published in 10.1021/acssuschemeng.5b01272
  2. 2.
    ISSN - Is published in 21680485

Journal

ACS Sustainable Chemistry and Engineering

Volume

4

Issue

3

Start page

1212

End page

1222

Total pages

11

Publisher

American Chemical Society

Place published

United States

Language

English

Copyright

© 2016 American Chemical Society

Former Identifier

2006061027

Esploro creation date

2020-06-22

Fedora creation date

2016-05-12

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