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For the sustainable reutilization of poultry feces (PF) to reduce environmental pollution, we present a novel approach for converting PF into a highly effective catalyst, consisting of trace copper (Cu) and sulfur (S) linked with ordered graphitized carbon (CS/CPF) for wastewater purification. Raman and EPR results verified that the disorderly organic matters in PF are transformed into orderly graphene structures that complexed with Cu to form large numbers of electron-poor/rich microregions on CS/CPF surface. The electrons from electron-rich organic pollutants can be directly captured by dissolved oxygen (DO) to produce abundant reactive oxygen species due to the enhanced electron polarization via the construction of Cu-S-C bond bridge on CS/CPF surface, which greatly enhance the removal efficiency of pollutants. CS/CPF achieves 100% removal for 2,4-dichlorophenoxyacetic acid (2,4-D) in just 10 min after adding trace peroxymonosulfate (PMS), keeping efficient catalytic activity after continuous reactions for 240 h. This strategy offers a practical and sustainable solution for the efficient resource recovery of poultry feces., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Excessive consumption of energy and resources is a major challenge in wastewater treatment. Here, a novel heterogeneous Fenton-like catalyst consisting of Cu-doped graphene-like catalysts (Cu-GCD NSs) was first synthesized by an enhanced carbothermal reduction of β-cyclodextrin (β-CD). The catalyst exhibits excellent Fenton-like catalytic activity for the degradation of various pollutants under neutral conditions, accompanied by low H 2 O 2 consumption. The results of structural characterization and theoretical calculations confirmed that the dual reaction centers (DRCs) were constructed on Cu-GCD NSs surface through C-O-Cu bonds supported on zero-valent copper species, which play a significant role in the high-performance Fenton-like reaction. The pollutants that served as electron donors were decomposed in the electron-poor carbon centers, whereas H 2 O 2 and dissolved oxygen obtained these electrons in the electron-rich Cu centers through C-O-Cu bonds, thereby producing more active species. This study demonstrates that the electrons of pollutants can be efficiently utilized in Fenton-like reactions by DRCs on the catalyst surface, which provides an effective strategy to improve Fenton-like reactivity and reduce H 2 O 2 consumption., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationship that could have appeared to influence the work reported in this article., (Copyright © 2022. Published by Elsevier B.V.)

The stable structure and toxic effect of refractory organic pollutants in wastewater lead to the problem of high energy consumption in water treatment technology. Herein, we propose a synergistic purification of refractory wastewater driven by microorganisms and surface microelectric fields (SMEF) over a dual-reaction-center (DRC) catalyst HCLL-S8-M prepared by an in situ growth method of carbon nitride on the Cu-Al 2 O 3 surface. Characterization techniques demonstrate the successful construction of SMEF with strong electrostatic force over HCLL-S8-M based on cation-π interactions between metal copper ions and carbon nitride rings. With the catalyst as the core filler, an innovative fixed bed bioreactor is constructed to purify the actual kitchen-oil wastewater. The removal efficiency of the wastewater even with a very low biodegradability (BOD 5 /COD = 0.33) can reach 60% after passing through this bioreactor. An innovative reaction mechanism is revealed for the first time that under the condition of a small amount of biodegradable organic matter, the SMEF induces the enrichment of electric active microorganisms (Desulfobulbus and Geobacter) in the wastewater, accelerates the interspecies electron transfer of intertrophic metabolism with the biodegradable bacteria through the extracellular electron transfer mechanism such as cytochrome C and self-secreted electron shuttle. The electrons of the refractory organic pollutants adsorbed on the surface of the catalyst are delocalized by the SMEF, which can be directly utilized by microorganisms through EPS conduction. The SMEF generated by electron polarization can maximize the utilization of pollutants and microorganisms in wastewater and further enhance degradation without adding any external energy, which is of great significance to the development of water self-purification technology., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Author(s). Published by Elsevier Ltd.. All rights reserved.)

Improper disposal of waste biomass and an increasing number of emerging contaminants (ECs) in water environment are universal threats to the global environment. Here, we creatively propose a sustainable strategy for the direct resource transformation of livestock manure (LM) into an innovative catalyst (Fe-CCM) for water self-purification with zero external consumption. ECs can be rapidly degraded in this self-purification system at ambient temperature and atmospheric pressure, without any external oxidants or energy input, accompanied by H 2 O and dissolved oxygen (DO) activation. The performance of the self-purification system is not affected by various types of salinity in the wastewater, and the corresponding second-order kinetic constant is improved 7 times. The enhanced water self-purification mechanism reveales that intermolecular forces between anions and pollutants reinforce electron exchange between pollutants and metal sites on the catalyst, further inducing the utilization of the intrinsic energy of contaminants, H 2 O, and DO through the interfacial reaction. This work provides new insights into the rapid removal of ECs in complicated water systems with zero external consumption and is expected to advance the resource utilization of livestock waste.

Herein, a novel metal-free catalyst consisting of multiporous oxygen-rich carbon-nitrogen graphene-like nanosheets (O LAA -CN NSs) is first developed through a staged temperature-programmed calcination of l-ascorbic acid (LAA)-modified dicyandiamide precursor. It is found that the oxygen species from l-ascorbic acid (O LAA ) are introduced into the graphene-like basic matrix and replace partial N atoms to form the COC-R structure, leading to the non-uniform distribution of electrons on the catalyst surface, and the formation of electron-rich centers around the COC microareas according to a series of characterization techniques. As a result, O LAA -CN NSs exhibits excellent performance for refractory pollutant removal in the presence of peroxymonosulfate (PMS) and dissolved oxygen. Some pollutants with complex structures are even completely degraded within only 1 min. The interface reaction mechanism is further revealed that PMS mainly acts as an active inducer to drive the electron donation of pollutants over O LAA -CN NSs. These electrons are finally utilized by dissolved oxygen to generate reactive oxygen species (ROS) through the interface process. This reaction system results in pollutants that can either be cleaved directly by surface oxidation process or degraded by the attack of the generated ROS, such as singlet oxygen ( 1 O 2 ) and superoxide radicals (O 2 •- ), through oxygen activation, which significantly reduces the resource and energy consumption in advanced wastewater treatment by harnessing the energy of pollutants and dissolved oxygen in the water., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Removing micropollutants in real water is a scientific challenge due to primary dissolved organic carbon (DOC) and high energy consumption of current technologies. Herein, we develop a self-purification process for the preferential destruction of various micropollutants in municipal wastewater, raw drinking water, and ultrapure water with humic acid (HA) driven by the surface microelectronic field of Fe 0 -Fe y C z /Fe x -GZIF-8-rGO without any additional input. It was verified that a strongly polar complex consisting of an electron-rich HA/DOC area and an electron-poor micropollutant area was formed between HA/DOC and micropollutants, promoting more electrons of micropollutants in the adsorbed complex to delocalizing to electron-rich Fe species area and be trapped by O 2 , which resulted in their surface cleavage and hydrolyzation preferentially. The higher micropollutant degradation efficiency observed in real wastewaters was due to the greater complex polarity of DOC. Moreover, the electron transfer process ensured the stability of the surface microelectronic field and continuous water purification. Our findings provide a new insight into low-energy combined-micropollution water treatment.

In common advanced oxidation processes, excess reagents and energy are often added to the reaction system to maintain the continuity of the reaction. These additions result in a large waste of resources and energy, which has become a bottleneck in the development of water treatment technology. In this study, we propose a new strategy to solve this problem based on a novel dual-reaction-center (DRC) Fe-ZnS quantum dots (Fe-ZnS QDs) catalyst that forms a non-equilibrium surface with an electron-polarized distribution. Through experimental and theoretical studies, it was verified that the activation of trace amounts of H 2 O 2 could break the energy barrier for pollutants to transfer electrons. The dissolved oxygen (DO) in the reaction system could be activated by gaining energy on the surface of the Fe-ZnS QDs catalyst, and was converted to 1 O 2 to attack organic pollution. In addition, the pollutants themselves supplied electrons to H 2 O 2 through the surface of the Fe-ZnS QDs catalyst to generate more •OH radicals for pollutant degradation, thus providing two fast paths for pollutant degradation. The system could drive the reaction through a trace amount of H 2 O 2 , thereby activating DO to generate 1 O 2 while effectively using the energy of pollutants. Therefore, the proposed system offers a new direction for the development of environmentally-friendly catalysts and greatly reduces the consumption of resources and energy., (Copyright © 2021 Elsevier B.V. All rights reserved.)

The effects of biological activated carbon treatment using Fe 2 O 3 modified coconut shell-based activated carbon (Fe/CAC) were investigated on the occurrence of opportunistic pathogens (OPs) and formation of disinfection by-products (DBPs) in simulated drinking water distribution systems (DWDSs) with unmodified CAC as a reference. In the effluent of annular reactor (AR) with Fe/CAC, the OPs growth and DBPs formation were inhibited greatly. Based on the differential pulse voltammetry and dehydrogenase activity tests, it was verified that extracellular electron transfer was enhanced in the attached biofilms of Fe/CAC, hence improving the microbial metabolic activity and biological removal of organic matter especially DBPs precursors. Meanwhile, the extracellular polymeric substances (EPS) on the surface of Fe/CAC exhibited stronger viscosity, higher flocculating efficiency and better mechanical stability, avoiding bacteria or small-scale biofilms falling off into the water. Consequently, the microbial biomass and EPS substances amount decreased markedly in the effluent of Fe/CAC filter. More importantly, Fe/CAC did significantly enhance the shaping role on microbial community of downstream DWDSs, continuously excluding OPs advantage and inhibiting EPS production. The weakening of EPS in DWDSs resulted in decrease of microbial chlorine-resistance ability and EPS-derived DBPs precursors supply. Therefore, the deterioration of water quality in DWDSs was inhibited greatly, sustainably maintaining the safety of tap water. Our findings indicated that optimizing biological activated carbon treatment by interface modification is a promising method for improving water quality in DWDSs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

The change of water quality was investigated in pilot-scale ozone-biological activated carbon (O 3 -BAC) filters using an emerging coconut shell-based granular activated carbon (CAC) or traditional granular activated carbon (GAC), respectively. More dissolved organic carbon (DOC) and disinfection by-products (DBPs) precursors were removed, meanwhile, less microbes, less metabolites and smaller microbial clusters were detected in the effluent of CAC compared with GAC. Sequentially, lower DBPs formation and higher disinfection efficiency were achieved in drinking water distribution systems (DWDSs). Furthermore, it was observed that extracellular electron transfer was enhanced in the attached biofilms of CAC, hence improving the microbial metabolic activity and biological removal of DOC. The results were attributed to the strong interaction of extracellular polymeric substances (EPS) with highly graphitized CAC. In addition, CAC resulted in totally different EPS in attached biofilms with superior characteristics including stronger viscosity, higher flocculating efficiency, mechanical stability and numerous binding sites for bacterial cells. Consequently, a wide range of compact interconnected biofilms formed on the surface of CAC and exhibited certain binding effect for microbial flocs and metabolites. Therefore, CAC resulted in higher microbial metabolic activity and lower release of microbes and metabolites, which was beneficial to maintain water quality safety in downstream DWDSs., Competing Interests: Declaration of Competing Interest The authors declare no conflict of interests., (Copyright © 2020. Published by Elsevier B.V.)

Drinking water distribution systems (DWDS) may be a "Trojan Horse" for some waterborne diseases caused by opportunistic pathogens (OPs). In this study, two simulated DWDS inoculated with groundwater were treated with chlorine (Cl 2 ) and ultraviolet/chlorine (UV/Cl 2 ) respectively to compare their effects on the OPs distributed in four different phases (bulk water, biofilms, corrosion products, and loose deposits) of DWDS. 16S rRNA genes sequencing and qPCR were used to profile microbial community and quantify target genes of OPs, respectively. Results showed that UV/Cl 2 was more effective than single Cl 2 to control the regrowth of OPs in the water with the same residual chlorine concentration. However, the OPs inhabiting the biofilms, corrosion products, and loose deposits seemed to be tolerant to UV/Cl 2 and Cl 2 , demonstrating that OPs residing in these phases were resistant to the disinfection processes. Some significant microbial correlations between OPs and Acanthamoeba were found by Spearman correlative analysis (p < 0.05), demonstrating that the ecological interactions may exist in the DWDS. 16S rRNA genes sequencing of water samples revealed a significant different microbial community structure between UV/Cl 2 and Cl 2 . This study may give some implications for controlling the OPs in the DWDS disinfected with UV/Cl 2 ., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Conventional water purification technologies struggle to simultaneously address purification efficiency and energy consumption. Molecular orbital level surface micro-electric field (MEF)-driven water purification is an original and innovative concept conceived and developed by our group in recent years. The core idea involves creating electron-rich and electron-poor micro-areas on the nanomaterial surface, which drive pollutants or H2O molecules to provide electrons in the electron-poor micro-areas while other environmental factors (such as H2O2 and O2) obtain electrons in the electron-rich micro-areas. This process effectively utilizes the internal energy contained within wastewater and emerging contaminants (ECs). Centered on this core, this review systematically examines the discovery, construction, and characteristics of MEF and MEF-like systems and summarizes their application directions. The challenges, bottlenecks, and future development directions of MEF technology are also analyzed and discussed. Reviews of MEFs can facilitate the development of low-consumption, high-efficiency water purification technologies.

The pre-designable structure and unique architectures of covalent organic frameworks (COFs) render them attractive as active and porous medium for water crisis. However, the effect of functional basis with different metrics on the regulation of interfacial behavior in advanced oxidation decontamination remains a significant challenge. In this study, we pre-design and fabricate different molecular interfaces by creating ordered π skeletons, incorporating different pore sizes, and engineering hydrophilic or hydrophobic channels. These synergically break through the adsorption energy barrier and promote inner-surface renewal, achieving a high removal rate for typical antibiotic contaminants (like levofloxacin) by BTT-DATP-COF, compared with BTT-DADP-COF and BTT-DAB-COF. The experimental and theoretical calculations reveal that such functional basis engineering enable the hole-driven levofloxacin oxidation at the interface of BTT fragments to occur, accompanying with electron-mediated oxygen reduction on terphenyl motif to active radicals, endowing it facilitate the balanced extraction of holes and electrons. The synergetic regulation of the electronic structure and interfacial reaction of covalent organic frameworks (COF) for water purification remains a challenge. Here the authors propose that COFs materials possessing molecular interfaces with ordered π skeletons, suitable pore size, and hydrophilic/hydrophobic channels synergically break through the adsorption energy barrier achieving high removal rates for micropollutants. [ABSTRACT FROM AUTHOR]

Rural pollution is largely caused by the accumulation of waste biomass, such as livestock manure and crop straw, which is extremely difficult to dispose of due to the simultaneous need to non-destructively treat metal and organic matter. Untreated fecal waste fluxes have contributed to more than 870,000 sanitation-related deaths annually worldwide. The existing disposal methods are accompanied by large amounts of energy and resource consumption and GHG emissions, which are not conducive to achieving the UN Sustainable Development Goals (SDGs). Herein, we pioneer a new approach to sustainable resource utilization by subjecting unprocessed livestock manure to a Dual-Reaction-Center (DRC) Fenton-like catalyst directly through the ordered bonding of intrinsic metal-organic species via an in situ 2-stage calcination-annealing process with zero emissions and zero pollution. The directional electron transfers along with the generated metal cation–π interactions during the resourcelized process led to the formation of electron-rich/-poor microregions. Through triggering by a small amount of hydrogen peroxide (H2O2), the removal of refractory pollutants reaches 100% within a very short time in this system, which also shows a long-term purification effect on actual wastewater, accompanied by the utilization of intrinsic energy from the pollutants and dissolved oxygen. This study is expected to advance the resource utilization of rural waste and the sustainable development of environmental factors. [ABSTRACT FROM AUTHOR]

• The Fenton-like Cu-PAN 3 catalysts is first synthesized by co-precipitation and carbon thermal reduction method. • Dual reaction centers are constructed around graphene-like carbon and Cu species. • The pollutants as electron donors inhibit the ineffective decomposition of H 2 O 2 at the electron-poor centers. • The pollutant removal mainly relies on the surface cleavage at the electron-poor centers. High energy consumption has seriously hindered the development of Fenton-like reactions for the removal of refractory organic pollutants in water. To solve this problem, we designed a novel Fenton-like catalyst (Cu-PAN 3) by coprecipitation and carbon thermal reduction. The catalyst exhibits excellent Fenton-like catalytic activity and stability for the degradation of various pollutants with low H 2 O 2 consumption. The experimental results indicate that the dual reaction centers (DRCs) are composed of Cu-N-C and Cu-O-C bridges between copper and graphene-like carbon, which form electron-poor/rich centers on the catalyst surface. H 2 O 2 is mainly reduced at electron-rich Cu centers to free radicals for pollutant degradation. Meanwhile, pollutants can be oxidized by donating electrons to the electron-poor C centers of the catalyst, which inhibits the ineffective decomposition of H 2 O 2 at the electron-poor centers. This therefore significantly reduces the consumption of H 2 O 2 and reduces energy consumption. [Display omitted] [ABSTRACT FROM AUTHOR]

A twofold cation-π-assembled catalyst consisting of honeycomb microsphere-like MoS 2 cross-linking g-C 3 N 4 hybrid (HM-MS/CN) is first developed to address the bottleneck of excessive resource and energy consumption in Fenton chemistry. A series of modern characterization techniques combined with theoretical calculation are used to reveal and verify the twofold cation-π interaction (Mo-O-C and Mo-S-C bonding bridges). It is found that the electrons of pollutants can be captured by H 2 O 2 and O 2 through the twofold cation-π interaction during Fenton-like reaction, which inhibits the oxidative decomposition of H 2 O 2 and promotes its hydroxylation. As a result, HM-MS/CN shows excellent performance for water purification by initiating pollutants as electron donors substituting H 2 O 2 consumption under mild natural conditions, and the actual consumption of H 2 O 2 in this system is only 6–8% of that in the common Fenton systems. This discovery is of great significance for the development of novel water purification technology with high efficiency and low consumption. [Display omitted] • A twofold cation-π-assembled catalyst consisting of HM-MS/CN is first prepared. • HM-MS/CN shows excellent performance for actual water purification. • The actual consumption of H 2 O 2 is only 6–8% of that in the common Fenton systems. • Twofold cation-π interaction based on Mo-O-C and Mo-S-C is responsible for excellent performance. • Pollutants act as electron donors substituting H 2 O 2 consumption via twofold cation-π. [ABSTRACT FROM AUTHOR]

Solid solution of BiOBr and BHO (BiO(OH) 0.06 Br 0.94 ) with abundant oxygen vacancies was supported on Ag/AgBr using precipitation and deposition–precipitation methods. The photocatalyst showed high and stable photocatalytic activity for the degradation of chlorophenols and azodyes in water under visible to NIR light irradiation without any release of Ag + , which came from visible-excited AgBr and the SPR of Ag NPs in the visible and NIR region. The different interfacial charge-transfer processes were verified on the basis of cyclic voltammetry analyses and all experimental information. The conduction band (CB) electrons of photoexcited AgBr reacted with the adsorbed oxygen forming O 2 •− , while the valence band (VB) holes of AgBr were transported the VB of BiO(OH) 0.06 Br 0.94 to oxidize organic pollutants or H 2 O to • OH. The plasmon-induced electrons from Ag NPs transferred to the CB of AgBr reacting with the adsorbed oxygen to O 2 •− , while the electrons trapped on the oxygen vacancies of BiO(OH) 0.06 Br 0.94 transferred to Ag NPs recombining with the plasmon-induced holes, inhibiting the release of Ag + , and the resulted VB holes of BiO(OH) 0.06 Br 0.94 oxidized organic compound. These interfacial charge transfers evidenced the high photoactivity and photostability of BiO(OH) 0.06 Br 0.94 /Ag/AgBr. [ABSTRACT FROM AUTHOR]

• Co2+-N-C π is constructed via atomically dispersed Co bonding with C-based graphene-like structure. • Co2+-N-C π (Co−π) structure plays key role for PMS activation and pollutant degradation. • Electron donation effect of pollutants is realized through π-π interaction in SACo-NGs system. • High efficiency and low consumption are realized in SACo-NGs/PMS water treatment system. Orbital interaction involving metal cation−π is an important form for electron transfer regulation. To accelerate the interfacial electron transfer of peroxymonosulfate (PMS) activation for water treatment, we report a new strategy through bonding atomically dispersed cobalt with nanospheric C-based graphene-like structures (SACo-NGs) to form metal cation−π structure, driving rapid and directional transfer of the electrons of pollutants to PMS on the catalyst surface. The catalyst SACo-NGs is synthesized by an enhanced hydrothermal-sintering method and the formation of metal cation−π structure is demonstrated by X-ray absorption fine structure (EXAFS), X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance spectroscopy (EPR) and Raman spectroscopy. It is found that Co−π structures (Co2+-N-C π) play a key role for the efficient activation of PMS, which results in pollutants being greatly removed in a few minutes. During the reaction, pollutants can donate electrons for the system through π−π interaction accompanying by the direct oxidative degradation of pollutants. The obtained electrons are quickly transferred to the atomically dispersed cobalt sites through the formed cation−π structure, which promotes the activation of PMS. This is a successful practice in the field of PMS activation using cation−π structure to accelerate electron transfer and achieve rapid degradation of pollutants. [ABSTRACT FROM AUTHOR]

[Display omitted] • HA was efficiently mineralized in an Fe0-Fe y C z /Fe x -GZIF-8-rGO aqueous suspension. • The polar alkane-alcohol complex was formed with more single electrons on –OH group. • The polar alkane-alcohol complex enhanced its surface cleavage and •OH formation. • The reaction kinetics depends on the surface complex characteristic. Natural organic matter (NOM) has diverse negative impacts on water purification, however, preventing them occurrence very difficult. Herein, humic acid (10 mg/L), as the main component of NOM, is completely destructed within 120 min in the Fe0-Fe y C z /Fe x -GZIF-8-rGO air-saturated aqueous suspension without additional energy input, while its mineralization is followed by three kinetic constants within 480 min. During the process, HA was first complexed with Fe0-Fe y C z /Fe x -GZIF-8-rGO by π-π interaction and H-bonding interaction and cleaved to aromatic compounds and then to alkanes and alcohols with some small acids before 120 min. The electron paramagnetic resonance (EPR) analysis and density functional theory (DFT) calculations confirmed that a strongly polarized alkane-alcohol complex was formed after 150 min with an electron-rich hydroxyl group area in alcohol and an electron-poor alkane area. Moreover, the more electrons of alkane in the complex are delocalized and trapped by O 2 , with the adsorption of the alkane-alcohol complex on the catalyst surface based on the analyses of both electrochemical impedance spectroscopy (EIS) and chronoamperometry, greatly promoting the surface cleavage and hydrolytic process of alkane in the complex and producing more •OH for pollutant degradation than it does from the HA surface complex, which results in the highest mineralization rate in the period of 150–390 min. Our findings demonstrated that the current system is very promising for complex mixture-containing water purification without additional energy. [ABSTRACT FROM AUTHOR]

A low-consumption water purification system is firstly constructed based on a new dual-reaction-center (DRC) catalyst molybdenum-doped zinc sulfide (Mo-ZnS, MZS) with a confined nonequilibrium surface. The extremely strong electron trapping ability of the Mo site is realized by the substitution of Mo for ZnS lattice. In this way, the electrons of emerging contaminants (ECs) are efficiently transferred to the nonequilibrium surface through the oriented interface process (Mo-S-Zn bond bridge), and obtained by the natural dissolved oxygen (DO) to generate hydrogen peroxide (H 2 O 2) under trace H 2 O 2 trigger without light and electricity assistant. The highest yield of H 2 O 2 is even up to ∼230 % of the initial value, and the ECs removal can reach 100 % within 60 min, which is far superior to conventional Fenton catalysts. This work realized the efficient utilization of the contaminant electrons through the construction of Mo-S-Zn bond bridge, which greatly reduced the energy consumption of water purification and improved the resourcefulness of ECs. [Display omitted] • DRC catalyst MZS with the confined nonequilibrium surface is first prepared. • MZS shows excellent performance for water purification. • Efficient H 2 O 2 generation is achieved without light and electricity assistant. • The highest H 2 O 2 concentration reaches up to ∼230 % of the initial concentration. • ECs electrons are efficiently utilized in ORR processes and water purification. [ABSTRACT FROM AUTHOR]

• Mesoporous reduction state cobalt species-doped silica nanospheres are first prepared. • Excellent activity is realized in mp -RSCo-SiO 2 NSs/H 2 O 2 system. • Efficient dual-pathway degradation of pollutant is achieved in Fenton-like process. • Pollutants replace H 2 O 2 as electron donors for the mp -RSCo-SiO 2 NSs system. • A new interfacial Fenton-like reaction mechanism involving pollutants is proposed. A novel heterogeneous Co-containing Fenton-like catalyst consisting of mesoporous reduction state cobalt (RSCo)-doped silica (SiO 2) nanospheres (mp -RSCo-SiO 2 NSs) was prepared by an enhanced hydrothermal process. The catalyst exhibited very high activity and stability for a series of refractory pollutant degradation in a very wide pH range of 3.1–10.9. The Fenton-like reaction rate constant of this Co-containing catalyst was approximately 290 times higher than that of Co 3 O 4 for pollutant degradation under the neutral and mild conditions. Based on the characterization, the catalyst possessed a porous nanosphere morphology, and the reduction state cobalt species, including nano-zero-valent cobalt (nZVCo) and Co2+, were found to be generated in the SiO 2 framework through forming Co O Si bonds. During the Fenton-like reaction, the electron donation effect of organic pollutants was successfully realized through the interaction of "Pollutants → Co2+/0-SiO 2 ". The obtained electrons from pollutants were transferred to the catalyst surface and captured by H 2 O 2 , resulting in the generation of hydroxyl radicals (OH). Therefore, a dual-pathway degradation of the pollutants was realized: (I) oxidation and degradation as the electron donors for the system and (II) attacking and destruction by OH radicals. This work provided a new perspective on the effective utilization of the electrons of pollutants and the improvement of Fenton reaction efficiency. [ABSTRACT FROM AUTHOR]

• Excellent activity for water purification is realized in cobalt-zinc ferrite/PMS system. • Surface oxygen vacancy induces PMS activation to generate •OH, SO 4 •− and H 2. • An efficient dual-pathway removal of pollutants is first achieved in PMS activation. • Pollutants replace PMS as electron donors for the V O -rich ZnFe 0.8 Co 0.4 O 2.4 system. • A novel solid-liquid interfacial reaction mechanism is proposed in PMS activation. Peroxymonosulfate (PMS) activation in heterogeneous processes for pollutant degradation is a promising water purification technology. However, the existed rate limiting step greatly restrains its performance and increases the consumption of PMS and energy. Herein, we offer a new strategy to solve this problem. In this work, surface oxygen vacancy (V O)-rich ZnFe 0.8 Co 0.4 O 2.4 nanoparticles were prepared and characterized, which exhibited high activity and stability for refractory pollutant degradation with PMS activation. It was found that PMS ([O 3 S O I O II H]−) could be adsorbed and trapped by the surface oxygen vacancies in the form of O I - Vo or O II - Vo during the reaction. Different electron transfer pathways from Vo to different O sites of PMS was realized in the solid-liquid interface based on the generation of OH, SO 4 − or H 2 from PMS reduction. Pollutants were predominantly adsorbed at metal Co sites in which their electrons were captured by metal species and then transferred to the surface oxygen vacancies, achieving efficient recycling of electrons in the aqueous suspensions. This system achieves a dual-pathway degradation of pollutants and electron transfer from pollutants to PMS to produce free radicals and H 2 , essentially changing the traditional concepts of pollutant removal and providing a sustainable strategy for pollutant utilization during water purification. [ABSTRACT FROM AUTHOR]

[Display omitted] • Zero-added conversion of chicken manure into water treatment catalyst (RCM) is realized. • Electron-poor/rich microregions are successfully constructed on RCM. • Pollutant degradation processes can be driven by a little bit of peroxymonosulfate. • RCM has excellent performance on actual wastewater treatment. • Water treatment with low consumption is achieved by utilization of pollutants. Fecal pollution in rural areas and water pollution caused by emerging contaminants (ECs) are two international environmental problems. Here, we propose a new strategy to address the two problems simultaneously through the resource utilization and harmless transformation of poultry manure as a kind of water purification catalyst with zero addition. The ordered bonding of intrinsic metal-organic species is realized in the resourcelized procedure by a one-stage calcination-annealing method, which results in the formation of electron-rich/poor microregions. With the triggering of a small amount of peroxymonosulfate (PMS), the energy/electrons of ECs are utilized by the dissolved oxygen in water driven by the electron-rich/poor microregions on the catalyst surface. As a result, the system exhibits excellent performance in removing various ECs. The degradation rate can even be maintained above 94.3 % after 10,000 cycles. This work indicates a sustainable approach to the effective utilization and treatment of rural waste and pollutants. [ABSTRACT FROM AUTHOR]

• Heterogeneous Fenton-like reaction was studied using a pilot scale test. • TCM, DCAA and TCAA were the main compositions of DBPs in drinking water. • C1-C5 and F1-F5 of NOM were the main precursors of different DBPs. • This treatment improved removal efficiency of DBPs and NOM without adjusting pH. • This treatment process also controlled the genotoxicity of drinking water. This paper explores the removal of natural organic matter (NOM) and disinfection by-products (DBPs) in drinking water by heterogeneous Fenton-like oxidation and granular activated carbon (GAC) filtration in a pilot scale test without adjusting pH of the water. pH of the used water in this study was from 7.5 to 8.7. Comparing with conventional water treatment processes, heterogeneous Fenton-like reaction and GAC filtration increased the removal rate of dissolved organic carbon (DOC), NOM with different apparent molecular weight (AMW) (F1-F7) and with different compositions (C1-C5) to 75.11%, 88.65% and 58.73%, respectively. Moreover, heterogeneous Fenton-like reaction and GAC filtration increased the removal rate of DBPs to 88.18%. The multivariate statistical analysis indicated that haloacetic acids (HAAs) and haloketones (HKs) mainly came from fulvic-like and humic-like NOM with AMW lower than 1.5 K Da. These substances with AMW between 1.5 K Da and 3.5 K Da were the main precursors of trihalomethanes (THMs). The main precursors of halonitriles (HANs) were soluble microbial byproduct-like (SMP-like), tyrosine-like and tryptophan-like substance with the AMW between 3.5 K Da and 4.5 K Da. Overall, without adjusting pH of water, heterogeneous Fenton-like reaction and GAC filtration improved the removal efficiency of NOM and DBPs, and controlled the genotoxicity of drinking water. [ABSTRACT FROM AUTHOR]