Sulfate radical-based advanced oxidation processes (SR-AOPs) employing heterogeneous catalysts to generate sulfate radical (SO4 −) from peroxymonosulfate (PMS) and persulfate (PS) have been extensively employed for organic contaminant removal in water. This article aims to provide a state–of–the–art review on the recent development in heterogeneous catalysts including single metal, mixed metal, and nonmetal carbon catalysts for organic contaminants removal, with particular focus on PMS activation. The hybrid heterogeneous catalyst/PMS systems integrated with other advanced oxidation technologies is also discussed. Several strategies for the identification of principal reactive radicals in SO4 −–oxidation systems are evaluated, namely (i) use of chemical probe or spin trapping agent coupled with analytical tools, and (ii) competitive kinetic approach using selective radical scavengers. The main challenges and mitigation strategies pertinent to the SR-AOPs are identified, which include (i) possible formation of oxyanions and disinfection byproducts, and (ii) dealing with sulfate produced and residual PMS. Potential future applications and research direction of SR-AOPs are proposed. These include (i) novel reactor design for heterogeneous catalytic system based on batch or continuous flow (e.g. completely mixed or plug flow) reactor configuration with catalyst recovery, and (ii) catalytic ceramic membrane incorporating SR-AOPs.

Generation of sulfate radical through heterogeneous catalysis for organic contaminants removal: Current development, challenges and prospects

Application of peroxymonosulfate and its activation methods for degradation of environmental organic pollutants: Review

Reports that promote persulfate-based advanced oxidation process (AOP) as a viable alternative to hydrogen peroxide-based processes have been rapidly accumulating in recent water treatment literature. Various strategies to activate peroxide bonds in persulfate precursors have been proposed and the capacity to degrade a wide range of organic pollutants has been demonstrated. Compared to traditional AOPs in which hydroxyl radical serves as the main oxidant, persulfate-based AOPs have been claimed to involve different in situ generated oxidants such as sulfate radical and singlet oxygen as well as nonradical oxidation pathways. However, there exist controversial observations and interpretations around some of these claims, challenging robust scientific progress of this technology toward practical use. This Critical Review comparatively examines the activation mechanisms of peroxymonosulfate and peroxydisulfate and the formation pathways of oxidizing species. Properties of the main oxidizing species are scrutinized and the role of singlet oxygen is debated. In addition, the impacts of water parameters and constituents such as pH, background organic matter, halide, phosphate, and carbonate on persulfate-driven chemistry are discussed. The opportunity for niche applications is also presented, emphasizing the need for parallel efforts to remove currently prevalent knowledge roadblocks.

/pdf/persulfate-based-advanced-oxidation-critical-assessment-of-ru3om4hbrg.pdf

Persulfate-Based Advanced Oxidation: Critical Assessment of Opportunities and Roadblocks.

Chemistry of persulfates in water and wastewater treatment: A review

The Fenton-like process presents one of the most promising strategies to generate reactive oxygen-containing radicals to deal with the ever-growing environmental pollution. However, developing improved catalysts with adequate activity and stability is still a long-term goal for practical application. Herein, we demonstrate single cobalt atoms anchored on porous N-doped graphene with dual reaction sites as highly reactive and stable Fenton-like catalysts for efficient catalytic oxidation of recalcitrant organics via activation of peroxymonosulfate (PMS). Our experiments and density functional theory (DFT) calculations show that the CoN4 site with a single Co atom serves as the active site with optimal binding energy for PMS activation, while the adjacent pyrrolic N site adsorbs organic molecules. The dual reaction sites greatly reduce the migration distance of the active singlet oxygen produced from PMS activation and thus improve the Fenton-like catalytic performance.

Single Cobalt Atoms Anchored on Porous N-Doped Graphene with Dual Reaction Sites for Efficient Fenton-like Catalysis

N-Doped graphene (NG) nanomaterials were synthesized by directly annealing graphene oxide (GO) with a novel nitrogen precursor of melamine. A high N-doping level, 8–11 at. %, was achieved at a moderate temperature. The sample of NG-700, obtained at a calcination temperature of 700 °C, showed the highest efficiency in degradation of phenol solutions by metal-free catalytic activation of peroxymonosulfate (PMS). The catalytic activity of the N-doped rGO (NG-700) was about 80 times higher than that of undoped rGO in phenol degradation. Moreover, the activity of NG-700 was 18.5 times higher than that of the most popular metal-based catalyst of nanocrystalline Co3O4 in PMS activation. Theoretical calculations using spin–unrestricted density functional theory (DFT) were carried out to probe the active sites for PMS activation on N-doped graphene. In addition, experimental detection of generated radicals using electron paramagnetic resonance (EPR) and competitive radical reactions was performed to reveal the PMS...

Nitrogen-Doped Graphene for Generation and Evolution of Reactive Radicals by Metal-Free Catalysis

A variety of dimensional-structured nanocarbons were applied for the first time as metal-free catalysts to activate persulfate (PS) for catalytic oxidation of phenolics and dyes as well as their degradation intermediates. Single-walled carbon nanotubes (SWCNTs), reduced graphene oxide (rGO), and mesoporous carbon (CMK-8) demonstrated superior catalytic activities for heterogeneous PS activation, whereas fullerene (C60), nanodiamonds, and graphitic carbon nitride (g-C3N4) presented low efficiencies. Moreover, the carbocatalysts presented even better catalytic performances than activated carbon and metal oxides, such as Fe3O4, CuO, Co3O4, and MnO2. The activity of prepared rGO-900 was further competing to the most efficient electron donor of zerovalent iron (ZVI). Both characterization and oxidation results suggested that the catalytic performances of the nanocarbons are determined by the intrinsic atom arrangements of carbon hybridization, pore structure, defective sites, and functional groups (especially ...

Insights into Heterogeneous Catalysis of Persulfate Activation on Dimensional-Structured Nanocarbons

Metal-free nanocarbon materials in different structural dimensions, such as 0D fullerene (C 60 ), 1D single-walled carbon nanotubes (SWCNTs), 2D graphene nanoplate (GNP), 3D hexagonally-ordered mesoporous carbon (CMK-3) and cubically-ordered mesoporous carbon (CMK-8) were investigated for adsorption and catalytic oxidation of phenol in water solutions. A variety of characterisation techniques were used to investigate the properties of the carbon samples. It was found that structural dimension and heat treatment would significantly affect the performance of the nanocarbons in adsorption and catalysis. Both GNP and CMK-3 showed better phenol adsorption with around 40% phenol removal in 500 mL of 20 ppm solutions. The nanocarbons were also used for metal-free activation of peroxymonosulfate (PMS) to produce sulfate radicals for catalytic phenol oxidation. Efficient catalysis was observed on CMK-3, CMK-8 and SWCNTs. Thermal treatment of the nanocarbons at 350 °C in nitrogen was conducted to modulate the crystal- and micro-structures and surface functional groups of the different nanocarbons. Enhancements at 2-fold in adsorption on SWCNTs and 7.5-fold in catalysis on CMK-8 were observed after the heat treatments. Mechanisms of adsorption and catalytic oxidation of phenol were discussed. This study contributes to the development of green materials for sustainable remediation of aqueous organic pollutants.

Nanocarbons in different structural dimensions (0–3D) for phenol adsorption and metal-free catalytic oxidation

New insights into heterogeneous generation and evolution processes of sulfate radicals for phenol degradation over one-dimensional α-MnO2 nanostructures

Nitrogen-doped reduced graphene oxide (N-rGO) was prepared by a simple process of simultaneous reduction and nitrogen doping on graphene oxide (GO) at low temperatures using ammonium nitrate as a N precursor. Characterization techniques indicated that N-rGO materials with a high N loading (5–8 at%) can be easily produced and that the crystal/micro-structures and chemical compositions of N-rGO materials are dependent on the calcination conditions. The metal-free catalysis of N-rGO was investigated by catalytic activation of peroxymonosulfate (PMS) for phenol oxidative degradation in water. It was found that N-rGO samples are promising green catalysts for phenol degradation. Kinetic studies showed that phenol degradation follows first order reaction kinetics on N-rGO-350 with an activation energy of 31.6 kJ mol−1. The mechanism of PMS activation and phenol oxidation was elucidated by employing both electron paramagnetic resonance (EPR) studies and quenching tests with ethanol and tert-butanol.

Stacey Indrawirawan

Papers

Nitrogen-Doped Graphene for Generation and Evolution of Reactive Radicals by Metal-Free Catalysis

Insights into Heterogeneous Catalysis of Persulfate Activation on Dimensional-Structured Nanocarbons

Nanocarbons in different structural dimensions (0–3D) for phenol adsorption and metal-free catalytic oxidation

New insights into heterogeneous generation and evolution processes of sulfate radicals for phenol degradation over one-dimensional α-MnO2 nanostructures

Low temperature combustion synthesis of nitrogen-doped graphene for metal-free catalytic oxidation