z-logo
Premium
Synergetic Behavior of TiO 2 ‐Supported Pd( z )Pt(1− z ) Catalysts in the Green Synthesis of Methyl Formate
Author(s) -
BaldovinoMedrano Víctor G.,
Pollefeyt Glenn,
Bliznuk Vitaliy,
Van Driessche Isabel,
Gaigneaux Eric M.,
Ruiz Patricio,
Wojcieszak Robert
Publication year - 2016
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201501211
Subject(s) - catalysis , x ray photoelectron spectroscopy , incipient wetness impregnation , methanol , methyl formate , microemulsion , formate , chemistry , nuclear chemistry , molar ratio , nanoparticle , inorganic chemistry , materials science , chemical engineering , nanotechnology , selectivity , organic chemistry , pulmonary surfactant , biochemistry , engineering
Methyl formate (MF) is a valuable platform molecule, the industrial production of which is far from being green. In this contribution, TiO 2 ‐supported Pd( z )Pt(1− z ) catalysts were found to be effective in the green synthesis of methyl formate (MF)—at T =323 K and ambient pressure—through methanol (MeOH) oxidation. Two series of catalysts with similar bulk Pd/(Pd+Pt) molar ratios, z , were prepared; one by a water‐in‐oil microemulsion (MicE) method and the other by an incipient wetness impregnation (IWI). The MicE method led to more efficient catalysts owing to a weak influence of z on particle size distributions and nanoparticles composition. Pd( z )Pt(1− z )‐MicE catalysts exhibited strong synergistic effects for MF production but weak synergistic effects for MeOH conversion. The catalytic performance of Pd( z )Pt(1− z )‐MicE was superior to that of Pd( z )Pt(1− z )‐IWI catalysts despite the latter displaying synergetic effects during the reaction. The catalytic behavior of TiO 2 ‐supported Pd( z )Pt(1− z ) catalysts was explained from correlations between XRD, TEM, and X‐ray photoelectron spectroscopy characterizations.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here