•  
  •  
 

Turkish Journal of Chemistry

Abstract

A series of alkylorganotin-based catalysts (Sn-g-C$_{3}$N$_{4}$/AC) was prepared by wet impregnation in ethanol using different g-C$_{3}$N$_{4}$ precursors and alkylorganotin compounds. The structure, texture, surface composition, and adsorption properties of the as-prepared catalysts were extensively characterized. Then, the obtained samples were evaluated for their catalytic performance in hydrochlorination of acetylene. The results provided by the X-ray photoelectron spectroscopy, acetylene temperature-programmed desorption, and HCl adsorption confirmed the nature of the active sites (i.e. Sn-N$_{x}$ ) involved in the reactant adsorption, and hence in the improved catalytic performance. These active sites were also related to the improved lifetime of alkylorganotin-based catalysts in the hydrochlorination of acetylene. At a constant reaction temperature of 200 °C with an acetylene gas hourly space velocity (C2H2-GHSV) of 30 h$^{-1}$, Sn-g$_{1}$ -C$_{3}$N$_{4}$/AC-550 exhibited the highest acetylene conversion (~98.0%) and selectivity toward the vinyl chloride monomer (>98.0%). From the catalytic test results, it was reasonably concluded that the hexamethylenetetramine is the most suitable N precursor, as compared to the dicyandiamide and urea, to prepare high-performance catalysts. From the BET specific surface area of fresh and used catalysts, it was suggested that, in contrast to dicyandiamide and urea, hexamethylenetetramine could delay the deposition of coke on alkylorganotin-based catalysts, which is reflected by the extended lifetime.

DOI

10.3906/kim-1909-64

Keywords

Alkylorganotin-based catalysts, g-C$_{3}$N$_{4}$, vinyl chloride, acetylene hydrochlorination

First Page

393

Last Page

408

Download

Included in

Chemistry Commons

Share

COinS