Removal of kathon by UV-C activated hydrogen peroxide:Kinetics,mechanisms,and enhanced biodegradability assessment

Kathon(CMI-MI),a mixture of 5-chloro-2-methyl-4-isothiazolin-3-one(CMI)and 2-methyl-4-isothiazolin-3-one(MI),was extensively used in industry as a nonoxidizing biocide or disinfectant.However,it would show adverse effects on aquatic life when it is discharged into surface water.In this study,the removal performance,parameter influence,degradation products and enhancement of subsequent biodegradation of CMI-MI in UV/H_(2)O_(2)system were systematically investigated.The degradation rate of CMI-MI could reach 90%under UV irradiation for 20 min when the dosage of H_(2)O_(2)was 0.3 mmol·L^(–1).The DOC(dissolved organic carbon)mineralization rate of CMI-MI could reach 35%under certain conditions([H_(2)O_(2)]=0.3 mmol·L^(–1),UV irradiation for 40 min).kobs was inversely proportional to the concentration of CMI-MI and proportional to the concentration of H_(2)O_(2).The degradation rate of CMIMI was almost unchanged in the pH range from 4 to 10.Except the presence of CO_(3)^(2-)inhibited the removal rate of CMI-MI,SO_(4)^(2-),Cl^(-),NO_(3)^(-),and NH_(4)^(+) did not interfere with the degradation of CMI-MI in the system.It was found that UV/H_(2)O_(2)system had lower energy consumption and more economic advantage compared with UV/PS system by comparing the EEO(electric energy per order)values under the same conditions.Two main organic products were identified,namely HCOOH and CH_(3)NH_(2).There’s also the formation of Cl^(-)and SO_(4)^(2-).After UV and UV/H_(2)O_(2)photolysis,the biochemical properties of CMI-MI solution were obviously improved,especially the UV/H_(2)O_(2)treatment effect was better,indicating that UV/H_(2)O_(2)technology is expected to combine with biotechnology to remove CMI-MI effectively and environmentally friendly from wastewater.

Progress and perspectives of Pd-based catalysts for direct synthesis of hydrogen peroxide

Hydrogen peroxide(H_(2)O_(2))is a green oxidant that has been widely used.The direct synthesis of hydrogen peroxide(DSHP)offers significant advantages in terms of high atomic economy and environmentally friendly effects.However,due to the inevitable side reactions and severe mass transfer limitations,it is still challenging to balance the selectivity and activity for the DSHP.Combining theoretical understanding with the controllable synthesis of nanocatalysts may significantly facilitate the design of“dream catalysts”for the DSHP.In this work,the main factors affecting the reaction performance of catalysts and the active sites of catalysts have been reviewed and discussed in detail.The development and design of catalysts with high efficiency were introduced from three aspects:the catalyst support,active component and atomic impurity.In addition,the coupling of DSHP and other oxidation reactions to realize one-pot in situ oxidation reactions was comprehensively emphasized,which showed essential guiding significance for the future development of H_(2)O_(2).

Photocatalytic and Electrocatalytic Generation of Hydrogen Peroxide: Principles, Catalyst Design and Performance

Hydrogen peroxide(H_(2)O_(2)) is a high-demand organic chemical reagent and has been widely used in various modern industrial applications. Currently,the prominent method for the preparation of H_(2)O_(2) is the anthraquinone oxidation.Unfortunately, it is not conducive to economic and sustainable development since it is a complex process and involves unfriendly environment and potential hazards. In this context, numerous approaches have been developed to synthesize H_(2)O_(2). Among them, photo/electro-catalytic ones are considered as two of the most promising manners for on-site synthesis of H_(2)O_(2). These alternatives are sustainable in that only water or O_(2) is required. Namely, water oxidation(WOR) or oxygen reduction(ORR)reactions can be further coupled with clean and sustainable energy. For photo/electro-catalytic reactions for H_(2)O_(2) generation, the design of the catalysts is extremely important and has been extensively conducted with an aim to obtain ultimate catalytic performance. This article overviews the basic principles of WOR and ORR,followed by the summary of recent progresses and achievements on the design and performance of various photo/electro-catalysts for H_(2)O_(2) generation. The related mechanisms for these approaches are highlighted from theoretical and experimental aspects. Scientific challenges and opportunities of engineering photo/electro-catalysts for H_(2)O_(2) generation are also outlined and discussed.

Synthesis of cystine C_(60) derivative and its protective effects on hydrogen peroxide-induced apoptosis in PC12 cells

Oxidative stress has been considered as a major cause of cellular injuries in a variety of clinical abnormalities, especially prominent in neural diseases. One of the usable ways to prevent the reactive oxygen species (ROS)-mediated cellular injury is dietary or pharmaceutical augmentation of some free radical scavenger. Water-soluble amino-fullerene is a novel compound that behaves as a free radical scavenger with excellent biology consistent. In the present study, we have synthesized and characterized a novel cystine C60 derivative for the first time, and investigated the effects on hydrogen peroxide-induced oxidative stress and apoptotic death in cultured rat pheochromocytoma (PC12) cells. PC12 cells treated with hydrogen peroxide underwent apoptotic death as determined by MTT, PI/Hoechst 33342 staining and flow cytometry analysis. These results suggested that cystine C60 derivative has the potential to prevent oxidative stress-induced cell death and has no evident toxicity.

Mathematical model and reaction mechanism of molybdenum and tungsten extraction with TRPO from peroxide solution

To understand the behavior of molybdenum and tungsten extracted by tri-alkyl phosphine oxide(TRPO)from peroxide solution,the extraction mechanism was studied by slope method and Raman and FTIR spectroscopy.The empirical formulas of molybdenum and tungsten extraction distribution ratio(D_(Mo)and D_(W))as functions of equilibrium pH,TRPO concentration and temperature were obtained by establishing mathematical models.Furthermore,the reliability of the empirical formula was verified in the H^(+)-W-Mo-H_(2)O_(2) solution.The results indicate that the calculated values of D_(Mo)or D_(W)were consistent with the experimental values.The apparent extraction equilibrium constants of molybdenum and tungsten wereK_(Mo)^(app)=8.51×10^(3)(0.74≤pH_(e)≤1.7),K_(Mo)^(app)=99.89×10^(3)(1.7<pH_(e)≤4.62)andK_(W)^(app)=2.65×10^(3)(0.92<pH_(e)<2.16)at 20°C,respectively.The main extraction complex of molybdenum or tungsten was[H_(2)(Mo or W)_(2)O_(3)(O_(2))_(4)(H_(2)O)_(2)]·2TRPO.These empirical formulas can be used to analyze and estimate the extraction and separation of Mo and W from low molybdenum and tungsten concentration solutions.

Recent Advances of Electrocatalyst and Cell Design for Hydrogen Peroxide Production

Electrochemical synthesis of H_(2)O_(2) via a selective two-electron oxygen reduction reaction has emerged as an attractive alternative to the current energy-consuming anthraquinone process. Herein, the progress on electrocatalysts for H_(2)O_(2) generation, including noble metal, transition metalbased, and carbon-based materials, is summarized. At first, the design strategies employed to obtain electrocatalysts with high electroactivity and high selectivity are highlighted. Then, the critical roles of the geometry of the electrodes and the type of reactor in striking a balance to boost the H_(2)O_(2) selectivity and reaction rate are systematically discussed. After that, a potential strategy to combine the complementary properties of the catalysts and the reactor for optimal selectivity and overall yield is illustrated. Finally, the remaining challenges and promising opportunities for highefficient H_(2)O_(2) electrochemical production are highlighted for future studies.

Revealing the concentration of hydrogen peroxide in fuel cell catalyst layers by an in‐operando approach

To evaluate the H_(2)O_(2)‐tolerance of non‐Pt oxygen reduction reaction(ORR)catalysts as well as in‐vestigate the H_(2)O_(2)‐induced decay mechanism,the selection of an appropriate H_(2)O_(2) concentration is a prerequisite.However,the concentration criterion is still unclear because of the lack of in‐operando methods to determine the actual concentration of H_(2)O_(2) in fuel cell catalyst layers.In this work,an electrochemical probe method was successfully established to in‐operando monitor the H_(2)O_(2) in non‐Pt catalyst layers for the first time.The local concentration of H_(2)O_(2) was revealed to reach 17 mmol/L,which is one order of magnitude higher than that under aqueous electrodes test conditions.Powered by the new knowledge,a concentration criterion of at least 17 mmol/L is suggested.This work fills in the large gap between aqueous electrode tests and the real fuel cell working conditions,and highlights the importance of in‐operando monitoring methods.

Eliminating H_(2)O/HF and regulating interphase with bifunctional tolylene-2,4-diisocyanate(TDI)additive for long life Li-ion battery

Lithium-ion batteries(LIBs)featuring a Ni-rich cathode exhibit increased specific capacity,but the establishment of a stable interphase through the implementation of a functional electrolyte strategy remains challenging.Especially when the battery is operated under high temperature,the trace water present in the electrolyte will accelerate the hydrolysis of the electrolyte and the resulting HF will further erode the interphase.In order to enhance the long-term cycling performance of graphite/LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM811)LIBs,herein,Tolylene-2,4-diisocyanate(TDI)additive containing lone-pair electrons is employed to formulate a novel bifunctional electrolyte aimed at eliminating H_(2)O/HF generated at elevated temperature.After 1000 cycles at 25℃,the battery incorporating the TDI-containing electrolyte exhibits an impressive capacity retention of 94%at 1 C.In contrast,the battery utilizing the blank electrolyte has a lower capacity retention of only 78%.Furthermore,after undergoing 550 cycles at 1 C under45℃,the inclusion of TDI results in a notable enhancement of capacity,increasing it from 68%to 80%.This indicates TDI has a favorable influence on the cycling performance of LIBs,especially at elevated temperatures.The analysis of the film formation mechanism suggests that the lone pair of electrons of the isocyanate group in TDI play a crucial role in inhibiting the generation of H_(2)O and HF,which leads to the formation of a thin and dense interphase.The existence of this interphase is thought to substantially enhance the cycling performance of the LIBs.This work not only improves the performance of graphite/NCM811 batteries at room temperature and high temperature by eliminating H_(2)O/HF but also presents a novel strategy for advancing functional electrolyte development.

A Novel Dual‑Channel Carbon Nitride Homojunction with Nanofibrous Carbon for Significantly Boosting Photocatalytic Hydrogen Peroxide Production

Photocatalytic H_(2)O_(2)synthesis(PHS)via graphite carbon nitride(g-C_(3)N_(4))is a low-carbon and environmentally friendly approach,which has garnered tremendous attention.However,as for the pristine g-C_(3)N_(4),the PHS is severely constrained by the slow transfer and rapid recombination of photogenerated carriers.Herein,we introduced cellulose-derived carbon nanofib-ers(CF)into the homojunction of g-C_(3)N_(4)nanotubes(MCN)and g-C_(3)N_(4)nanosheets(SCN).A series of photocatalytic results demonstrate that the embedding of cellulose-derived carbon for MCN/SCN/CF composite catalyst significantly improved the photocatalytic H_(2)O_(2)generation(136.9μmol·L^(-1)·h^(-1))with 5-holds higher than that of individual MCN(27.5μmol·L^(-1)·h^(-1))without any sacrificial agent.This enhancement can be attributed to the combined effects of the two-step one-electron oxy-gen reduction reaction(ORR)on conduction band(CB)side and the water oxidation reaction(WOR)on valence band(VB)side.A comprehensive characterization of the mechanism indicates that CF enhances the absorption of light,promotes the separation and migration of photogenerated carriers,and regulates the position of the valence and conduction bands with an effective dual-channel ORR pathway for photo-synthesis of H_(2)O_(2).This work provides valuable insights into utilizing biomass-based materials for significantly boosting photocatalytic H_(2)O_(2)production.

Effect of Copper Sources and Levels on Hydrogen Peroxide Generation by Mitochondria from Broiler Liver

The present experiment was performed with the objective of examining the effects of copper sources and levels on hydrogen peroxide(H_2O_2) generation by mitochondria from broiler hepatocytes. Treatments were applied to compare sources of copper(CuSO_4 versus Cu-Met) and 4 levels of dietary Cu (11,110,220 and 330 mg/kg).Day-old broilers(Cobb 500,Gallus domesticus,n=288) were randomly divided into 8 groups of 36 each and fed diets as follows:Controls(Cu 11 mg/kg) and high copper(Cu 110, 220,and 330 mg/kg),for 60 days under normal conditions.Sample collections were made at 12,36 and 60 days of age to investigate the changes in H_2O_2 generation by mitochondria from hepatocytes.Compared with those of the control diets,H_2O_2 generation by mitochondria in the high copper groups(110 to 330 mg/kg) of the two copper sources were increased(P<0.05 or P<0.01);At days 36 and 60,H_2O_2 generation by hepatic mitochondria from Cu-Met supplementation exceeded that from birds supplemented with CuSO_4 (P<0.05 or P<0.01).In addition,H_2O_2 generation by mitochondria from broilers fed with high dietary copper appeared to be associated with altered function of mitochondrial complexⅣ.The results indicated that dietary supplementation with copper induced oxidative stress damage in liver.At each level of copper supplementation,the organic Cu-Met led to more rapid H_2O_2 generation than did inorganic CuSO_4.The results also suggest that mitochondrial complexⅣmay be targeted under conditions of high dietary copper supplementation.

Involvement of the ABA-and H_(2)O_(2)-Mediated Ascorbate-Glutathione Cycle in the Drought Stress Responses of Wheat Roots

Abscisic acid(ABA),hydrogen peroxide(H_(2)O_(2)) and ascorbate(AsA)–glutathione(GSH)cycle are widely known for their participation in various stresses.However,the relationship between ABA and H_(2)O_(2) levels and the AsA–GSH cycle under drought stress in wheat has not been studied.In this study,a hydroponic experiment was conducted in wheat seedlings subjected to 15%polyethylene glycol(PEG)6000–induced dehydration.Drought stress caused the rapid accumulation of endogenous ABA and H_(2)O_(2) and significantly decreased the number of root tips compared with the control.The application of ABA significantly increased the number of root tips,whereas the application of H_(2)O_(2) markedly reduced the number of root tips,compared with that under 15%PEG-6000.In addition,drought stress markedly increased the DHA,GSH and GSSG levels,but decreased the AsA levels,AsA/DHA and GSH/GSSG ratios compared with those in the control.The activities of the four enzymes in the AsA–GSH cycle were also markedly increased under drought stress,including glutathione reductase(GR),ascorbate peroxidase(APX),monodehydroascorbate reductase(MDHAR)and dehydroascorbate reductase(DHAR),compared with those in the control.However,the application of an ABA inhibitor significantly inhibited GR,DHAR and APX activities,whereas the application of an H_(2)O_(2) inhibitor significantly inhibited DHAR and MDHAR activities.Furthermore,the application of ABA inhibitor significantly promoted the increases of H_(2)O_(2) and the application of H_(2)O_(2) inhibitor significantly blocked the increases of ABA,compared with those under 15% PEG-6000.Taken together,the results indicated that ABA and H_(2)O_(2) probably interact under drought stress in wheat;and both of them can mediate drought stress by modulating the enzymes in AsA–GSH cycle,where ABA acts as the main regulator of GR,DHAR,and APX activities,and H_(2)O_(2) acts as the main regulator of DHAR and MDHAR activities.

Bioscillation and Birhythmicity in the H_2O_2-KSCN-CuSO_4-NaOH System

Two kinds of different mechanistic oscillations can be displayed in the H_2O_2-KSCN-CuSO_4-NaOH system. One discovered by this study is the pH oscillation in a continuous flow stirred tank reactor(CSTR) resulting from the oxidation of KSCN. The other is the oscillation of H_2O_2 decomposition in both CSTR and batch reactors(reported by Orbáin in 1986). Under appropriate experimental conditions, the system exhibits a birhythmicity in a CSTR. Two different pH oscillations are reported here. The pH oscillations which accompany the decomposition of H_2O_2 exist in the batch reactor and the CSTR at a high flowrate, but the pH oscillations in a CSTR at a low flowrate originates from proton positive and negative feedback in the oxidation of KSCN. The oscillation of non-catalyzed oxidation of KSCN by hydrogen peroxide in a CSTR can be found. Also we have observed whether Cu^(2+) exists or not in the batch system, the pH increases to near neutral ultimately after pH drops twice.

Harvesting the Vibration Energy of CdS for High-Efficient Piezo-Photocatalysis Removal of U(Ⅵ):Roles of Shape Dependent and Piezoelectric Polarization

Piezo-photocatalysis could coalesce the advantages of mechanical vibration and solar energy perfectly to achieve high-efficiency catalytic activity.Herein,the quintessential piezoelectric material CdS nanowires with different aspect ratios are precisely constructed and applied for piezo-photocatalytic reduction of U(Ⅵ)for the first time.The ultrasonic(60 kHz,100 W)induces piezoelectric potential to generate a 0.57 eV A^(-1)electric field,which is added to the direction of CdS(010)as a driving force to efficiently separate photogenerated charges.The alliance between piezoelectric effect and photocatalytic activity endows CdS NW-3 with the fastest piezo-photocatalytic rate under ultrasonic vibration and 5 W LED irradiation,and the relevant rate constant(0.042 min^(-1))is about 12 and 53.8 times than that of LED and ultrasonication.More importantly,93.74%of U(Ⅵ)could be removed from natural uranium mine wastewater.Therefore,this piezo-photocatalysis system that reduces U(Ⅵ)to easily separable(UO_(2))O_(2)·2H_(2)O(s)provides valuable input for disposal applications of radioactive wastewater and broadens the horizons of nuclear energy utilization toward the advancement of carbon neutrality.

Exploring the Roles of Single Atom in Hydrogen Peroxide Photosynthesis

This comprehensive review provides a deep exploration of the unique roles of single atom catalysts(SACs)in photocatalytic hydrogen peroxide(H_(2)O_(2))production.SACs offer multiple benefits over traditional catalysts such as improved efficiency,selectivity,and flexibility due to their distinct electronic structure and unique properties.The review discusses the critical elements in the design of SACs,including the choice of metal atom,host material,and coordination environment,and how these elements impact the catalytic activity.The role of single atoms in photocatalytic H_(2)O_(2)production is also analysed,focusing on enhancing light absorption and charge generation,improving the migration and separation of charge carriers,and lowering the energy barrier of adsorption and activation of reactants.Despite these advantages,several challenges,including H_(2)O_(2)decomposition,stability of SACs,unclear mechanism,and low selectivity,need to be overcome.Looking towards the future,the review suggests promising research directions such as direct utilization of H_(2)O_(2),high-throughput synthesis and screening,the creation of dual active sites,and employing density functional theory for investigating the mechanisms of SACs in H_(2)O_(2)photosynthesis.This review provides valuable insights into the potential of single atom catalysts for advancing the field of photocatalytic H_(2)O_(2)production.

Self-assembled S-scheme In_(2.77)S_(4)/K^(+)-doped g-C_(3)N_(4)photocatalyst with selective O_(2) reduction pathway for efficient H_(2)O_(2) production using water and air

The development of an efficient artificial H_(2)O_(2) photosynthesis system is a challenging work using H_(2)O and O_(2) as starting materials.Herein,3D In_(2.77)S_(4) nanoflower precursor was in-situ deposited on K^(+)-doped g-C_(3)N_(4)(KCN)nanosheets using a solvothermal method,then In_(2.77)S_(4)/KCN(IS/KCN)het-erojunction with an intimate interface was obtained after a calcination process.The investigation shows that the photocatalytic H_(2)O_(2) production rate of 50IS/KCN can reach up to 1.36 mmol g^(-1)h^(-1)without any sacrificial reagents under visible light irradiation,which is 9.2 times and 4.1 times higher than that of KCN and In_(2.77)S_(4)/respectively.The enhanced activity of the above composite can be mainly attributed to the S-scheme charge transfer route between KCN and In_(2.77)S_(4) according to density functional theory calculations,electron paramagnetic resonance and free radical capture tests,leading to an expanded light response range and rapid charge separation at their interface,as well as preserving the active electrons and holes for H_(2)O_(2) production.Besides,the unique 3D nanostructure and surface hydrophobicity of IS/KCN facilitate the diffusion and transportation of O_(2) around the active centers,the energy barriers of O_(2) protonation and H_(2)O_(2) desorption steps are ef-fectively reduced over the composite.In addition,this system also exhibits excellent light harvesting ability and stability.This work provides a potential strategy to explore a sustainable H_(2)O_(2) photo-synthesis pathway through the design of heterojunctions with intimate interfaces and desired reac-tion thermodynamics and kinetics.

Polypyride intercalation boosting the kinetics and stability of V_(3)O_(7)·H_(2)O cathodes for aqueous zinc-ion batteries

V_(3)O_(7)·H_(2)O(VO)is a high capacity cathode material in the field of aqueous zinc ion batteries(AZIBs),but it is limited by slow ion migration and low electrical conductivity.In this paper,polypyridine(PPyd)intercalated VO with nanoribbon structure was prepared by a simple in-situ pre-intercalation,which is noted VO-PPyd.The total density of states(TDOS)shows that after the pre-intercalation of PPyd,an intermediate energy level appears between the valence band and conduction band,which provides a step that can effectively reduce the band gap and enhance the electron conductivity.Furthermore,the density functional theory(DFT)results found that Zn^(2+)is more easily de-intercalated from the V-O skeleton,which proves that the embeddedness of PPyd improves the diffusion kinetics of Zn^(2+).Electrochemical studies have shown that VO-PPyd cathode materials exhibit excellent rate performance(high specific capacity of 465 and 192 mA h g^(-1)at 0.2 and 10 A g^(-1),respectively)and long-term cycling performance(92.7%capacity retention rate after 5300 cycles),due to their advantages in structure and composition.More importantly,the energy density of VO-PPyd//Zn at 581 and 5806 W kg^(-1)is 375 and 247 W h kg^(-1),respectively.VO-PPyd exhibits excellent electrochemical properties compared to previously reported vanadium based cathodes,which makes it highly competitive in the field of high-performance cathode materials of AZIBs.

Building stabilized Cu_(0.17)Mn_(0.03)V_(2)O_(5−□)·2.16H_(2)O cathode enables an outstanding room‐/low‐temperature aqueous Zn‐ion batteries

Vanadium oxide cathode materials with stable crystal structure and fast Zn^(2+) storage capabilities are extremely important to achieving outstanding electrochemical performance in aqueous zinc‐ion batteries.In this work,a one‐step hydrothermal method was used to manipulate the bimetallic ion intercalation into the interlayer of vanadium oxide.The pre‐intercalated Cu ions act as pillars to pin the vanadium oxide(V‐O)layers,establishing stabilized two‐dimensional channels for fast Zn^(2+) diffusion.The occupation of Mn ions between V‐O interlayer further expands the layer spacing and increases the concentration of oxygen defects(Od),which boosts the Zn^(2+) diffusion kinetics.As a result,as‐prepared Cu_(0.17)Mn_(0.03)V_(2)O_(5−□)·2.16H_(2)O cathode shows outstanding Zn‐storage capabilities under room‐and lowtemperature environments(e.g.,440.3 mAh g^(−1) at room temperature and 294.3 mAh g^(−1)at−60°C).Importantly,it shows a long cycling life and high capacity retention of 93.4%over 2500 cycles at 2 A g^(−1) at−60°C.Furthermore,the reversible intercalation chemistry mechanisms during discharging/charging processes were revealed via operando X‐ray powder diffraction and ex situ Raman characterizations.The strategy of a couple of 3d transition metal doping provides a solution for the development of superior room‐/lowtemperature vanadium‐based cathode materials.

V_(2)O_(3)/VO_(2)@S/N-C nanofibers with excellent cycling stability and superior rate capability in aqueous zinc ion batteries

The development of aqueous zinc-ion batteries (AZIBs) marks a significant advancement in the field of sustainable and environmentally friendly energy storage.To address the challenges faced by singlephase vanadium-based oxides,such as poor conductivity and dissolution in electrolytes,this study introduces vacuum S/N doping to fabricate V_(2)O_(3)/VO_(2)@S/N-C nanofibers,improving the cycling stability and enhancing the capacity.The V_(2)O_(3)/VO_(2)@S/N-C electrode exhibits exceptional cyclic stability,retaining a capacity of 133.3 m A h g^(-1)after 30,000 cycles at a high current density of 100 A g^(-1)and a capacity retention of 81.8%after 150,000 cycles at 200 A g^(-1).Characterizations using ex-situ X-ray diffraction and ex-situ X-ray photoelectron spectroscopy reveal co-intercalation of H^(+)and Zn^(2+)in the V_(2)O_(3)/VO_(2)@S/N-C electrode.Due to the presence of S_(2)^(2-),more phases changed to V_(10)O_(24).12H_(2)O,making the V_(2)O_(3)/VO_(2)@S/N-C electrode better reversible.By elucidating the zinc storage mechanism and demonstrating the stable performance of the doped electrode,this work contributes valuable insights into the optimization of the electrode materials for future energy storage solutions.

H_2O_2氧化体系在燃煤锅炉烟气净化中的应用研究进展

介绍了H_2O_2氧化体系在燃煤锅炉烟气多种污染物一体化脱除技术中的反应机理及应用研究进展,对芬顿体系或类芬顿体系的液相氧化、类气相均相氧化和非均相催化活化在燃煤锅炉烟气脱硫、脱硝、脱汞上的应用进行了详细讨论,并分析了紫外线、添加剂等辅助手段和催化剂分别对均相和非均相氧化体系的影响规律及作用机理,最后根据燃煤烟气治理技术的研究进展及燃煤烟气多种污染物一体化脱除技术的发展需要,提出研发活化H_2O_2催化剂和添加剂是今后燃煤锅炉烟气净化的重要研究方向。

UV/H_2O_2和UV/TiO_2降解磺胺甲噁唑的研究

采用UV/H_2O_2和UV/TiO_2两种工艺降解磺胺甲噁唑(SMX),确定了H_2O_2和TiO_2的最佳投加量,在保持最佳投加量的条件下研究了SMX初始浓度、反应溶液初始pH、叔丁醇投加量对两种方法降解SMX效果的影响,为研究两种方法在降解SMX过程中的矿化程度测定了TOC的去除情况。结果表明,两种方法都对SMX具有较好的去除效果,整体而言UV/H_2O_2对SMX的降解速率高于UV/TiO_2;UV/H_2O_2的降解速率更易受到SMX初始浓度、反应溶液初始pH的影响;UV/H_2O_2对SMX的降解过程中·OH的氧化作用和UV直接降解都是去除SMX的主要作用,而UV/TiO_2中UV直接降解和空穴直接氧化是去除SMX的主要作用。