Facile synthesis of pyrite FeS2 on carbon spheres for high-efficiency Fenton-like reaction.

Designing iron-based catalysts for Fenton-like reactions with peroxymonosulfate (PMS) as oxidants have attracted growing attentions. Herein, pyrite FeS2 supported on carbon spheres (FeS2@C) is synthesized by a facile low-temperature method. The FeS2@C/PMS system can degrade carbamazepine (CBZ) effectively in a wide pH range. Sulfate radicals (SO4·-), hydroxyl radicals (·OH), superoxide radical (O2·-), and singlet oxygen (1O2) are the responsible reactive oxygen species (ROSs) for CBZ degradation. Moreover, in the simulated fixed-bed reactor, the FeS2@C/PMS system can maintain a high CBZ removal ratio of >95% for than 8 h, exhibiting its excellent stability. The outstanding performance of FeS2@C/PMS system is attributed to the presence of carbon spheres and lattice S2-, which together promote the Fe(III)/Fe(II) redox cycle. The FeS2@C is a promising catalyst due to its facile synthesis, low cost, high efficiency, and excellent stability to activate PMS for organics degradation.

Coating CoFe2O4 shell on Fe particles to increase the utilization efficiencies of Fe and peroxymonosulfate for low-cost Fenton-like reactions.

Bimetallic composites (Fe@CoFe2O4) with zero-valent Fe as the core encapsulated by CoFe2O4 layers are synthesized by a coprecipitation-calcination method, which are applied to activate PMS for the degradation of bisphenol A (BPA). Enhanced activity of Fe@CoFe2O4 is achieved with very fast degradation rate (kobs = 0.5737 min-1). In the fixed-bed reactor, the catalyst lifetime (tul) of Fe@CoFe2O4 is determined to be 22 h compared to 11 h of Fe, and the deactivation rate constant (kd) for Fe@CoFe2O4 is 0.0083 mg·L-1·h-1, only ∼1/10 of Fe (0.0731). The XPS results indicate that the core-shell structure of Fe@CoFe2O4 could promote the redox cycles of Co3+/Co2+ and Fe3+/Fe2+. It is proved that the coating of CoFe2O4 shell on Fe0 can protect the Fe0 core from being oxidized by PMS to form passivation layer. The electrons of Fe0 can therefore be used effectively for activating PMS to produce ROSs via the CoFe2O4 shell. This modification method of Fe0 would decrease the cost of PMS based wastewater remediation greatly, thus should have great potential on an industrial scale.

Lithium Iron Phosphate and Layered Transition Metal Oxide Cathode for Power Batteries: Attenuation Mechanisms and Modification Strategies.

In the past decade, in the context of the carbon peaking and carbon neutrality era, the rapid development of new energy vehicles has led to higher requirements for the performance of strike forces such as battery cycle life, energy density, and cost. Lithium-ion batteries have gradually become mainstream in electric vehicle power batteries due to their excellent energy density, rate performance, and cycle life. At present, the most widely used cathode materials for power batteries are lithium iron phosphate (LFP) and LixNiyMnzCo1-y-zO2 cathodes (NCM). However, these materials exhibit bottlenecks that limit the improvement and promotion of power battery performance. In this review, the performance characteristics, cycle life attenuation mechanism (including structural damage, gas generation, and active lithium loss, etc.), and improvement methods (including surface coating and element-doping modification) of LFP and NCM batteries are reviewed. Finally, the development prospects of this field are proposed.

Facile synthesis of iron oxide supported on porous nitrogen doped carbon for catalytic oxidation.

Iron oxide (FexOy) supported on porous nitrogen doped carbon is synthesized by a facile pyrolysis method. SiO2 and NaNO3 are used as the template and activation agent respectively for porous structure generation and large specific surface area (SSA) creation. The obtained materials show superior catalytic oxidation ability and can activate peroxymonosulfate (PMS) in a wide pH range (3-9) to degrade organic pollutants. The degradation process is a two-stage reaction, including a rapid initial decay and a following slow reaction stage. According to the free radical quenching experiments, electron paramagnetic resonance (EPR) spectroscopy analysis, and electrochemical tests, the superoxide radical (O2-) and singlet oxygen (1O2) are proved to play crucial roles in organics degradation. The high SSA (773 m2 g-1), abundant of structural defects, and synergistic effect between FexOy and the nitrogen doped carbon are the key factors for the enhanced activity. The catalysts in this study can be synthesized easily and contain no toxic metals, thus should have great potential in the wastewater remediation.

Porous SiO2 coated AlxFeyZr1-x-yO2 solid superacid nanoparticles with negative charge for polyvinylidene fluoride (PVDF) membrane: Cleaning and partial desalinating seawater.

In this work, porous SiO2 coated AlxFeyZr1-x-yO2 solid superacid nanoparticles with negative charge (CS-SAFZr) were synthesized via hydrolysis, sulfation and sulfonation, and characterized by SEM, TEM, XRD, BET and so on. The results show that the size of CS-SAFZr nanoparticles prepared under the optimum preparation conditions is around 80 nm, thickness of the porous SiO2 shell is about 20 nm, Hammett acidity is -16.197 and ion exchange capacity (IEC) is 0.98 mmol·g-1. Correspondingly, ferrum (Fe) and aluminum (Al) elements are successfully doped into the ZrO2 lattice and the doped nanoparticles present a specific surface area of 396.2 m2 g-1 with abundant hydroxyl and sulfonic acid groups on the surface. To investigate the properties of the nanoparticles as the filler, polyvinylidene fluoride (PVDF) was used as a candidate to prepare CS-SAFZr/PVDF ultrafiltration (UF) composite membranes and the performance were characterized via cleaning and desalinating seawater. Results indicate that the CS-SAFZr nanoparticles strengthen their compatibility with the membrane via hydrogen bonds and improve performances of PVDF membrane. The suspended solid and conductivity decline ratio of permeate seawater was 1.8 mg L-1 and 13.20% respectively, indicating that CS-SAFZr/PVDF membrane performs seawater cleaning and partial desalination. Therefore, CS-SAFZr nanoparticles can be a promising candidate to modify PVDF membrane for cleaning and desalinating seawater.