Synergetic Manipulation Mechanism of Single-Atom M-N and M-OH (M = Mn, Fe, Co, Ni) Sites for Ozone Activation: Theoretical Prediction and Experimental Verification.

Carbon-based single-atom catalysts (SACs) have been gradually introduced in heterogeneous catalytic ozonation (HCO), but the interface mechanism of O activation on the catalyst surface is still ambiguous, especially the effect of a surface hydroxyl group (M-OH) at metal sites. Herein, we combined theoretical calculations with experimental verifications to comprehensively investigate the O activation mechanisms on a series of conventional SAC structures with N-doped nanocarbon substrates (MN-NCs, where M = Mn, Fe, Co, Ni). The synergetic manipulation effect of the metal atom and M-OH on O activation pathways was paid particular attention.

Proton transfer triggered in-situ construction of C=N active site to activate PMS for efficient autocatalytic degradation of low-carbon fatty amine.

Removal of low-carbon fatty amines (LCFAs) in wastewater treatment poses a significant technical challenge due to their small molecular size, high polarity, high bond dissociation energy, electron deficiency, and poor biodegradability. Moreover, their low Brønsted acidity deteriorates this issue. To address this problem, we have developed a novel base-induced autocatalytic technique for the highly efficient removal of a model pollutant, dimethylamine (DMA), in a homogeneous peroxymonosulfate (PMS) system.

A sustainable process for selective recovery of metals from gallium-bearing waste generated from LED industry.

With the rapid development of the LED industry, gallium (Ga)-bearing waste generated is regarded as one of the most hazardous as it typically contains heavy metals and combustible organics. Traditional technologies are characterized by long processing routes, complex metal separation processes and significant secondary pollution emission. In this study, we proposed an innovative and green strategy to selectively recovery Ga from Ga-bearing waste by using a quantitative phase-controlling transition process.

Insight into the Mechanism of Cobalt-Nickel Separation Using DFT Calculations on Ethylenediamine-Modified Silica Gel.

The separation of Co(II) and Ni(II) from leaching solution is gaining interest because Co(II) and Ni(II) are increasingly used in emerging strategic areas, such as power batteries. Herein, the surface of silica gel is functionalized with 1,2-ethylenediamine and used for the separation of Co(II) and Ni(II). The Co(II) removal efficiency of the modified silica is 80.

A sustainable approach for selective recovery of lithium from cathode materials of spent lithium-ion batteries by induced phase transition.

Recycling of spent lithium-ion batteries (LIBs) has attracted widespread attention because of their dual attributes to environmental protection and resource conservation. Utilization of strong corrosive acids is currently the preferred way to recover valuable metals from spent LIBs, but the extensive use of chemical reagents can pose serious environmental risks. Herein, this research proposes a green process for selective recovery of lithium using the material of spent LIBs itself without adding exogenous reagents, mechanochemistry induced phase transition.

Novel catalysts with multivalence copper for organic pollutants removal from wastewater with excellent selectivity and stability in Fenton-like process under neutral pH conditions.

Fenton-like reaction has been widely used for organics degradation. However, most Fenton-like reaction works at low pH range (pH < 4) with uncontrollable selectivity of hydroxyl radicals from H O activation, and unsatisfied catalyst stability, which is compromised advanced oxidation performance for water/wastewater treatments. In this work, to solve the drawbacks, novel copper catalysts were fabricated via hydrogen reduction/calcination of Cu -supported Al/MCM-41 with precisely controllable copper valence state.

Pretreatment of membrane dye wastewater by CoFe-LDH-activated peroxymonosulfate: Performance, degradation pathway, and mechanism.

When a membrane is used to treat dye wastewater, dye molecules are continually concentrated at the membrane surface over time, resulting in a dramatic decrease in membrane flux. Aside from routine membrane cleaning, the pretreatment of dye wastewater to degrade organic pollutants into tiny molecules is a facile solution to the problem. In this study, the use of layered double hydroxide (LDH) to activate peroxymonosulfate (PMS) for efficient degradation of organic pollutant has been thoroughly investigated.

Bioaugmentation of quinoline-degrading bacteria for coking wastewater treatment: performance and microbial community analysis.

sp. XKL1, previously found to have the ability to efficiently degrade quinoline, was bioaugmented into a lab-scale A/O/O system to treat real coking wastewater. During the bioaugmentation stage, the removal of quinoline and pyridine of the O1 tank could be enhanced by 9.

Insights into the Mechanism of Ozone Activation and Singlet Oxygen Generation on N-Doped Defective Nanocarbons: A DFT and Machine Learning Study.

N-doped defective nanocarbon (N-DNC) catalysts have been widely studied due to their exceptional catalytic activity in many applications, but the O activation mechanism in catalytic ozonation of N-DNCs has yet to be established. In this study, we systematically mapped out the detailed reaction pathways of O activation on 10 potential active sites of 8 representative configurations of N-DNCs, including the pyridinic N, pyrrolic N, N on edge, and porphyrinic N, based on the results of density functional theory (DFT) calculations. The DFT results indicate that O decomposes into an adsorbed atomic oxygen species (O) and an O on the active sites.

The structure-activity relationship of aromatic compounds in advanced oxidation processes：a review.

Advanced oxidation processes (AOPs) are widely used as efficient technologies to treat highly toxic and harmful substances in wastewater. Taking the most representative aromatic compounds (monosubstituted benzenes, substituted phenols and heterocyclic compounds) as examples, this paper firstly introduces their structures and the structural descriptors studied in AOPs before, and the influence of structural differences in AOPs with different reactive oxygen species (ROS) on the degradation rate was discussed in detail. The structure-activity relationship of pollutants has been previously analyzed through quantitative structure-activity relationship (QSAR) model, in which ROS is a very important influencing factor.

Open-Framework Metal Oxides for Fast and Reversible Hydrated Zinc-Ion Intercalation.

The development of high capacity and stable cathodes is the key to the successful commercialization of aqueous zinc-ion batteries. However, significant solvation penalties limit the choice of available positive electrodes. Herein, hydrated intercalation is proposed to promote reversible (de)intercalation within host materials by rationally designing a matching electrode.

Photoinduced release of odorous volatile organic compounds from aqueous pollutants: The role of reactive oxygen species in increasing risk during cross-media transformation.

Photoinduced volatile organic compounds (VOCs) release from fatty alcohols at the air-water interface, has attracted considerable attention. This paper comprehensively explores the release of odorous VOCs from aqueous micropollutants under photoirradiation, especially in terms of the important role of the reactive oxygen species (ROS) in increased risk by cross-media transformation. The formation and distribution of photoinduced VOCs produced by aqueous benzyl alcohol (BzOH), a common ingredient in personal care products, were monitored in situ by online gas chromatography equipped with mass spectrometry and flame ionization detector (GC-MS/FID).

Bipolar Membrane Electrodialysis for Ammonia Recovery from Synthetic Urine: Experiments, Modeling, and Performance Analysis.

Recovering nitrogen from source-separated urine is an important part of the sustainable nitrogen management. A novel bipolar membrane electrodialysis with membrane contactor (BMED-MC) process is demonstrated here for efficient recovery of ammonia from synthetic source-separated urine (∼3772 mg N L). In a BMED-MC process, electrically driven water dissociation in a bipolar membrane simultaneously increases the pH of the urine stream and produces an acid stream for ammonia stripping.

Enhanced nitrogen removal upon the addition of volatile fatty acids from activated sludge by combining calcium peroxide and low-thermal pretreatments.

This study investigated a combined low-thermal and CaO pretreatment to enhance the volatile fatty acid (VFA) production from waste activated sludge (WAS). The fermentative product was added to a sequencing batch reactor (SBR) as an external carbon source to enhance nitrogen removal. The results showed that the combined pretreatment improved WAS solubilization, releasing more biodegradable substrates, such as proteins and polysaccharides, from TB-EPS to LB-EPS and S-EPS.

Review on strategies of close-to-natural wetland restoration and a brief case plan for a typical wetland in northern China.

Wetlands play an important role in sustaining ecosystems on the earth, which regulate water resources, adjust local climate and produce food for human beings, etc. However, wetlands are facing huge challenges due to human activities and other natural evolution, such as area shrinkage, function weakening and biodiversity decrease, and so on, therefore, some wetlands need to be urgently restored. In this study, the main technology components of close-to-natural restoration of wetlands were summarized.

Criticality assessment of metal resources in China.

With the development of modern industries, the sustainability of critical resources has attracted worldwide attention considering the entire supply chain. With a large industrial sector size in China, a safe supply of metal resources is crucial to ensure the effective operation of the whole industry. Although specific criticality analyses have been applied to identify critical resources in some regions, including Europe and the USA, they are not ready to be directly applied in the case of China because the structure of China's industry is remarkably different from other areas.

Photoinduced Release of Volatile Organic Compounds from Fatty Alcohols at the Air-Water Interface: The Role of Singlet Oxygen Photosensitized by a Carbonyl Group.

Photoinduced interfacial release of volatile organic compounds (VOCs) from surfactants receives emerging concerns. Here, we investigate the photoreaction of 1-nonanol (NOL) as a model surfactant at the air-water interface, especially for the important role of O in the formation of VOCs. The production of VOCs is real-time quantitated.

Investigation of MOF-derived humidity-proof hierarchical porous carbon frameworks as highly-selective toluene absorbents and sensing materials.

Carbon frameworks (CFs) derived from metal-organic frameworks (MOFs) have been produced as adsorbents of toluene. To further obtain optimum hierarchical porous carbon structure of CFs, different treatment temperatures were applied to a typical kind of MOFs (ZIF-8). The adsorption capacity of the toluene of hierarchical porous CFs obtained from ZIF-8 under 1100 °C (CF-1100, adsorption capacity of 208.

Catalytic oxidation of CO on noble metal-based catalysts.

Carbon monoxide (CO) catalytic oxidation has gained increasing interest in recent years due to its application prospects. The noble metal catalysts commonly exhibit outstanding CO catalytic oxidation activity. Therefore, this article reviewed the recent research on the application of noble metal catalysts in the catalytic oxidation of CO.

Performance prediction of ZVI-based anaerobic digestion reactor using machine learning algorithms.

The use of zero-valent iron (ZVI) to enhance anaerobic digestion (AD) systems is widely advocated as it improves methane production and system stability. Accurate modeling of ZVI-based AD reactor is conducive to predicting methane production potential, optimizing operational strategy, and gathering reference information for industrial design in place of time-consuming and laborious tests. In this study, three machine learning (ML) algorithms, namely random forest (RF), extreme gradient boosting (XGBoost), and deep learning (DL), were evaluated for their feasibility of predicting the performance of ZVI-based AD reactors based on the operating parameters collected in 9 published articles.

O oxidation excited by yellow phosphorus emulsion coupling with red mud absorption for denitration.

Directing to unwieldiness NOx emitted by the industry, the removal of NOx was implemented using yellow phosphorus (P) emulsion and red mud slurry as composite absorbent. Where yellow phosphorus is considered to stimulate formation of the ecological ozone (O) from O, the oxidation of insoluble NO into water-soluble NOx species by O, and the red mud as a pH buffer can be used to maintain the pH of the absorption liquid in a range that better absorbs NOx. NO is finally converted into NO and NO, whereas the yellow phosphorus is mainly PO.

Coupling mechanism of activated carbon mixed with dust for flue gas desulfurization and denitrification.

To clarify the effect of coking dust, sintering dust and fly ash on the activity of activated carbon for various industrial flue gas desulfurization and denitrification, the coupling mechanism of the mixed activated carbon and dust was investigated to provide theoretical reference for the stable operation. The results show that coking dust had 34% desulfurization efficiency and 10% denitrification efficiency; correspondingly, sintering dust and fly ash had no obvious desulfurization and denitrification activities. For the mixture of activated carbon and dust, the coking dust reduced the desulfurization and denitrification efficiencies by blocking the pores of activated carbon, and its inhibiting effect on activated carbon was larger than its own desulfurization and denitrification activity.

Coupling-oxidation process promoted ring-opening degradation of 2-mecapto-5-methyl-1,3,4-thiadizaole in wastewater.

As an important raw material and intermediate of widely used antibiotics cefazolin and cefazedone, 2-mecapto-5-methyl-1,3,4-thiadizaole (MMTD) in antibiotic wastewater is hardly decyclized during wastewater treatment, posing great risk to the environment. This work proposed a green "coupling-oxidation" process to enhance ring-opening of MMTD during antibiotic wastewater treatment. In particular, the significant role of humic substances (HS) as pre-coupling reagent was emphasized.

Reactive Oxygen Species and Catalytic Active Sites in Heterogeneous Catalytic Ozonation for Water Purification.

Heterogeneous catalytic ozonation (HCO) processes have been widely studied for water purification. The reaction mechanisms of these processes are very complicated because of the simultaneous involvement of gas, solid, and liquid phases. Although typical reaction mechanisms have been established for HCO, some of them are only appropriate for specific systems.

Conversion Mechanisms of Selective Extraction of Lithium from Spent Lithium-Ion Batteries by Sulfation Roasting.

With the undergoing unprecedented development of lithium-ion batteries (LIBs), the recycling of end-of-life batteries has become an urgent task considering the demand for critical materials, environmental pollution, and ecological impacts. Selective recovery of targeted element(s) is becoming a topical field that enables metal recycling in a short path with highly improved material efficiencies. This research demonstrates a process of selective recovery of spent Ni-Co-Mn (NCM)-based lithium-ion battery by systematically understanding the conversion mechanisms and controlling the sulfur behavior during a modified-sulfation roasting.