Boron Nitride-Confined Nanographene as a Metal-Free Catalyst for Acetylene Hydrochlorination
Xiaoqiang Guo1,2, Yihan Ye1,2, Guangzong Fang1,2
1State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023, P. R. China.
Abstract:
Substitution of toxic mercury catalysts for the manufacture of vinyl chloride monomer (VCM) via acetylene hydrochlorination is a global initiative. We report herein boron nitride matrix-confined nanographene (BNC) as a metal-free catalyst, which is characterized by abundant B-N-C active sites at the interconnected nanographene-boron nitride domains. Their unique electronic structure facilitates the adsorption and polarization of linear acetylene molecules, as evidenced by microscopic elemental analysis and spectroscopic characterization, as well as theoretical calculations. Acetylene conversion increases almost linearly with the content of B-N-C sites. An optimized catalyst enables almost complete conversion of acetylene and 99% VCM selectivity, and it delivers stable performance within an 800 h test at 260 °C and 45 h-1. Notably, even at an elevated space velocity up to 230 h-1, acetylene conversion and VCM selectivity still reach 99%. It outperforms conventional nitrogen-doped carbon and boron nitride catalysts. This BNC catalyst shows great potential for the sustainable production of vinyl chloride.
Related Concept Videos
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Hydroboration-Oxidation of Alkenes
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Catalysis
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...


