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Mercury emission from industrial activities has become a major environmental health concern, because mercury is one of the most toxic metals encountered in the environment. Elemental mercury is the dominant Hg species in gas streams. Adsorption is regarded as a practical technique for Hg0 removal, for which developing efficient and economic adsorbents are needed. Chalcogenides have recently gained increasing research interest owing to their high binding affinity for Hg0. Chalcogen-based adsorbents include S-modified adsorbents, H2S- and SO2-activated adsorbents, polysulfide chalcogels, mineral sulfides and metal selenides. This article reviews chalcogen-based adsorbents for Hg0 capture from gas streams, with focus on removal performances, mechanisms, advantages and disadvantages. Results show that S modification, and H2S and SO2 activation generate a great variety of active sulfur species on the adsorbent surface, resulting in enhanced Hg0 removal activity. Sulfur species include elemental sulfur, sulfide, thiophene and sulfate. Nonetheless, removal efficiency decreases to some extent due to the presence of acidic flue gas components and steam. On the other hand, mineral sulfides and metal selenides exhibit outstanding Hg0 removal performances with fast adsorption rate, high mercury capacity and excellent resistance to SO2 and H2O. Yet most mineral sulfides and metal selenides perform well below 100 °C, which might limit industrial applications.

CO2 emission is partly responsible for climate change induced by greenhouse effects. Carbon capture, utilization and storage is a major pathway to reduce CO2 emission. This article reviews conversion of CO2 into value-added products by photocatalytic, electrocatalytic and photoelectrocatalytic processes, which involve a catalyst, a reducing agent, an electrolyte and a reactor. An ideal catalyst should be cheap, abundant, non-toxic, less corrosive and chemically stable. Doping various catalysts can increase product yields up to 207 times. Furthermore, monolith reactors generated 23 times and 14 times higher yields than slurry and cell reactors, respectively. Photoelectrocatalytic conversion standout because it combines the advantages of photocatalytic and electrocatalytic processes such as high product yield and selectivity, no electrical energy required, cost-effectiveness, more catalysts option and no sacrificial donor.

Air pollution caused by mercury emissions from combustion and pyrolysis of fossil fuels, biomass, and solid wastes is a major health issue. Elemental mercury (Hg0), the dominant species in flue gas, is poorly captured by actual control equipments because Hg0 has a high volatility and is insoluble in water. Alternatively, photocatalytic processes can oxidize Hg0 into Hg compounds that are easier to remove. Here we review the recent research on oxidative removal of Hg0 by photocatalysts, with focus on titanium dioxide, bismuthides, silver compounds and hybrid photocatalysts. We discuss the Hg0 removal performances and mechanisms of catalytic oxidation. The TiO2 photocatalyst often suffers from low absorption of solar energy and easy recombination of photoinduced electron–hole couples. BiOIO3 appears as a promising photocatalyst due to its high Hg0 oxidation activity under visible light irradiation. Silver carbonates and silver halides are newly developed visible-light-responsive photocatalysts for Hg0 removal. Fast separation and transformation of photogenerated electrons and holes control the performance of Hg0 removal by photocatalysts.

Integrated gasification combined cycle (IGCC) and solid oxide fuel cell (SOFC) systems are considered as the most promising clean coal technologies. Syngas derived from coal gasification is the major fuel sources for IGCC and SOFC power systems; however, large amounts of sulfur compounds, mainly in the form of hydrogen sulfide, are produced during gasification. Hydrogen sulfide has to be removed prior to syngas utilization to protect downstream equipment from high-temperature corrosion. Therefore, hydrogen sulfide removal from raw syngas plays a key role in successful application of IGCC and SOFC systems. Hot coal gas desulfurization using solid sorbents is a more efficient technique for hydrogen sulfide removal, compared with conventional cold coal gas desulfurization with amine solution. This article reviews solid sorbents for high-temperature desulfurization, e.g., transition metal oxides, rare-earth oxides, spinel oxides, perovskite oxides, nanoelemental metals and mesoporous desulfurizers. Composite oxides that combine the properties of diverse metal oxides are promising candidates for hot coal gas desulfurization. The extensive background knowledge and the state of the art on high-temperature sorbents for hydrogen sulfide removal in this review provides inspiration and guidance to develop new cost-effective sorbents.