Chloromethanes are a group of volatile organic compounds that are harmful to the environment and human health. Abundant studies have verified that hydrodechlorination might be an effective treatment to remove these chlorinated pollutants. The most outstanding advantages of this technique are the moderate operating conditions used and the possibility of obtaining less hazardous valuable products. This review presents a global analysis of experimental and theoretical studies regarding the hydrodechlorination of chloromethanes. The catalysts used and their synthesis methods are summarized. Their physicochemical properties are analyzed in order to deeply understand their influence on the catalytic performance. Moreover, the main causes of the catalyst deactivation are explained, and prevention and regeneration methods are suggested. The reaction systems used and the effect of the operating conditions on the catalytic activity are also analyzed. Besides, the mechanisms and kinetics of the process at the atomic level are reviewed. Finally, a new perspective for the upgrading of chloromethanes, via hydrodechlorination, to valuable hydrocarbons for industry, such as light olefins, is discussed.

Dichloromethane (DCM) is an important pollutant with very harmful effects on human health and the environment. Catalytic hydrodechlorination (HDC) is an environmentally friendly technology for its removal from gas streams; it avoids the formation of hazardous pollutants like dioxins and phosgene (produced by other techniques), and the products obtained can be reused in other industries. When compared to other precious metals, Pd/C catalyst exhibited a better catalytic activity. However, the catalyst showed a significant deactivation during the reaction. In this study, the oxidation state and particle size of Pd was monitored with time on stream in order to elucidate the transformations that the catalyst undergoes during HDC. The deactivation can be ascribed to the formation of a new PdC x phase during the first hour of reaction. Carbon atoms incorporated to Pd lattice come from (chloro)-hydrocarbons adsorbed in the metallic species, whose transformation is promoted by the HCl originating in the reaction. Nevertheless, the catalyst was regenerated by air flow treatment at 250 • C, recovering the catalyst more than 80% of initial DCM conversion.

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Functionalized carbon nanofibers (CNF) are fascinating materials to be used as supports in Pd-based catalysts for the treatment of waste chloroform (TCM) to produce light olefins through the catalytic hydrodechlorination (HDC). The CNF were functionalized by HNO3, HCl, and urea. Compared to the Pd supported on un-treated CNF, all the catalysts using functionalized CNF as support showed lower turnover frequency values with higher stability, owing to their smaller Pd nanoparticles (NPs). These smaller Pd NPs are formed due to the stronger metal–support interactions promoted by the higher concentration of surface groups on the functionalized catalysts. Since the smaller Pd NPs could hinder the hydrogenation of olefins to paraffins, the selectivity to olefins increased on the functionalized catalysts. Moreover, the N-doped CNF was successfully formed on the catalyst functionalized by urea. Since the nitrogen functional groups (pyridinic N and pyrrolic N) could provide much stronger metal–support interactions compared to the oxygen functional groups on the other catalysts, the catalyst functionalized by urea showed the smallest Pd NPs among the four catalysts, leading to the highest selectivity to light olefins.

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