Activated Carbon-Supported Tetrapropylammonium Perruthenate Catalysts for Acetylene Hydrochlorination

Activated Carbon Supported Mo-Ti-N Binary Transition Metal Nitride as Catalyst for Acetylene Hydrochlorination

Recently, many scientists have focused on the development of green industrial technology. However, the process of synthesizing vinyl chloride faces the problem of Hg pollution. Via a novel approach, we used two elements Mo and Ti to prepare an inexpensive and green binary transition metal nitride (BTMN) as the active ingredient in a catalyst with nano-sized particles and an excellent degree of ...

Aqua regia activated Au/C catalysts for the hydrochlorination of acetylene

Characterization of Au species in Au/C catalysts for the hydrochlorination reaction of acetylene

A set of Au/C catalysts for the gas phase hydrochlorination of acetylene to vinyl chloride monomer were prepared using a range of strong acids as impregnating solvents and varying the preparation drying temperature. The most active catalyst is the material prepared using aqua regia as solvent with an intermediate drying temperature of 140 C. The effects of the catalyst preparation parameters on...

Recovery of Palladium from Spent Activated Carbon-Supported Palladium Catalysts

TÜBİTAK Marmara Research Center, Chemistry Institute, 41470 Gebze, Kocaeli, Turkey Email: [email protected] Activated carbon-supported palladium catalysts are liable to progressive deactivation even in the absence of any gaseous contaminants during the oxidation of hydrogen under ambient conditions. The high value of palladium coupled with environmental considerations means that n...

Identification of single-site gold catalysis in acetylene hydrochlorination.

There remains considerable debate over the active form of gold under operating conditions of a recently validated gold catalyst for acetylene hydrochlorination. We have performed an in situ x-ray absorption fine structure study of gold/carbon (Au/C) catalysts under acetylene hydrochlorination reaction conditions and show that highly active catalysts comprise single-site cationic Au entities who...