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Conventional biological nitrogen removal (BNR) processes for mainstream municipal wastewater (MMW) treatment have high energy and chemical costs. Partial nitritation/anammox (PN/A) has the potential to reduce the carbon footprint of BNR; however, its implementation for MMW treatment has been limited by the low ammonium and high organic matter concentrations in MMW, which prevent suppression nitrite oxidizing bacteria (NOB) and heterotrophic denitrifiers. In this study, after organic carbon diversion, ammonium was separated from MMW in a novel bench-scale sequencing batch biofilm reactor (SBBR) containing chabazite, a natural zeolite mineral with a high ammonium ion exchange (IX) capacity. After breakthrough, chabazite was bioregenerated by PN/A biofilms. Recirculation was applied from the bottom to the top of the column to create an aerobic zone (top) for ammonia-oxidizing microorganisms (AOM) and an anoxic zone (bottom) for anammox bacteria. Rapid IX-PN/A SBBR startup was observed after inoculation with PN/A enrichments. The time required for bioregeneration decreased with increasing recirculation rate, with high total inorganic nitrogen (TIN) removal efficiency (81 %) and ammonium removal rate (0.11 g N/L/day) achieved at recirculation velocity of 1.43 m/h. The core microbiome of the IX-PN/A SBBR contained a high abundance of bacteria of the phylum Pseudomonadota (15.27–20.62 %), Patescibacteria (12.38–20.05 %), Chloroflexota (9.36–14.23 %), and Planctomycetota (7.55–12.82 %), while quantitative PCR showed the highest ammonia monooxygenase (amoA, 2.0 × 102) and anammox copy numbers (amx, 1.0 × 104) in the top layers. The single-stage IX-PN/A SBBR achieved stable BNR for >two years without chemical inputs, media replacement or brine waste production. 

Metal oxynitrides demonstrate promising activity for photocatalytic solar water splitting and CO2 reduction under solar irradiance aided by noble metals. Precise control of cation ratios in the oxynitrides is a necessary challenge needed to overcome for achieving effective band gap tuning. Here we report density functional theory-based calculations on intricate structure-function relationships of Zn-Ga based oxynitrides and correlate results with the experimental parameters. Crucial material property descriptors such as elemental composition, intrinsic lattice strain, and vacancy defects were exploited during the synthesis to achieve stable oxynitride photocatalysts that demonstrated CO2 conversion to CO under simulated solar spectrum, without any noble metal impregnation. The highest CO production rate surpassed that of TiO2 under the same conditions. This work inspires future research on oxynitride materials towards tailored optical properties and sustainable photocatalytic activity enabling large scale applications. 

Conversion of CO 2 in a scalable technology has the potential for enormous energy and environmental impact but remains a challenge. We present several stable, earth abundant perovskite oxide materials for the reverse water gas shift chemical looping (RWGS-CL) process as a potential solution for this CO 2 mitigation problem. This material and process combination circumvents issues plaguing other emerging technologies, viz. poor rates of CO 2 conversion, high operation temperatures, use of precious metal catalysts, or combinations thereof. Using DFT-calculated oxygen vacancy formation energy, a key descriptor for the RWGS-CL process, we have successfully predicted several earth abundant perovskite oxides with high CO 2 conversion capability. We simultaneously achieved 100% selective CO generation from CO 2 at the highest known rates (∼160 μmoles per min per gram perovskite oxide) at record low process temperatures of 450–500 °C using lanthanum and calcium based perovskite oxides. These materials are stable over several RWGS-CL cycles, enabling industrial implementation. 

Current society is inherently based on liquid hydrocarbon fuel economies and seems to be so for the foreseeable future. Due to the low rates (photocatalysis) and high capital investments (solar-thermo-chemical cycles) of competing technologies, reverse water gas shift (rWGS) catalysis appears as the prominent technology for converting CO 2 to CO, which can then be converted via CO hydrogenation to a liquid fuel of choice (diesel, gasoline, and alcohols). This approach has the advantage of high rates, selectivity, and technological readiness, but requires renewable hydrogen generation from direct (photocatalysis) or indirect (electricity and electrolysis) sources. The goal of this review is to examine the literature on rWGS catalyst types, catalyst mechanisms, and the implications of their use CO 2 conversion processes in the future.