Effects of support composition and pretreatment on the activity and selectivity of carbon-supported PdCu n Cl x catalysts for the synthesis of diethyl carbonate

PdCu n Cl x species dispersed on carbon supports catalyze the oxidative carbonylation of ethanol to diethyl carbonate (DEC). Catalyst activity and selectivity are improved by oxidation of the carbon support before preparation, and catalyst stability can be achieved by the addition of ppm levels of CCl 4 into the feed. It is proposed that the highest activity is exhibited by Cl-bridged [CuCl 2]Pd[CuCl 2] species. The oxidative carbonylation of ethanol to diethyl carbonate (DEC) has been investigated on catalysts prepared by dispersing CuCl 2 and PdCl 2 on activated carbon and carbon nanofibers. The objectives of this work were to establish the effects of support structure and pretreatment on the dispersion of the catalytically active components and, in turn, on the activity and selectivity of the catalyst for DEC synthesis. At the same surface loading of CuCl 2 and PdCl 2, partially oxidized carbon nanofibers resulted in a higher dispersion of the active components and a higher DEC activity than could be achieved on activated carbon. Catalyst characterization revealed that nearly atomic dispersion of CuCl 2 and PdCl 2 could be achieved on the edges of the graphene sheets comprising the carbon nanofibers. Over oxidation of the edges or their removal by heat treatment of the nanofibers resulted in a loss of catalyst activity. The loss of catalyst activity with time on stream could be overcome by the addition of ppm levels of CCl 4 to the feed. While catalysts prepared with CuCl 2 alone were active, a fivefold increase in activity was realized by using a PdCl 2/CuCl 2 ratio of 1/20. It is proposed that the Pd 2+ cations interact with [CuCl 2] − anions to form Pd[CuCl 2] 2 complexes that are stabilized through dative bonds formed with oxygen groups present at the edges of the graphene sheets of the support. A mechanism for DEC synthesis is discussed, and a role for the Pd 2+ cations as part of this mechanism is proposed.