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Identification and ecotoxicity assessment of intermediates generated during the degradation of clofibric acid by advancedoxidation processes

Wenzhen LI, Yu DING, Qian SUI, Shuguang LU, Zhaofu QIU, Kuangfei LIN

《环境科学与工程前沿（英文）》 2012年 第6卷 第4期   页码 445-454 doi: 10.1007/s11783-012-0419-6

摘要： The aim of this study was to identify the intermediates in clofibric acid degradation under various advanced oxidation processes, namely ultraviolet (UV), UV/H O , vacuum ultraviolet (VUV), VUV/H O , and solar/TiO processes, as well as to assess the toxicity of these intermediates. Eleven intermediates have been detected by gas chromatography-mass spectrometer, most of which were reported for the first time to our best knowledge. Combining the evolution of the dissolved organic carbon, Cl and specific ultraviolet absorption at 254 nm, it could be deduced that cleavage of aromatic ring followed by dechlorination was the mechanism in solar/TiO process, while dechlorination happened first and accumulation of aromatic intermediates occurred in the other processes. Different transformation pathways were proposed for UV-, VUV-assisted and solar/TiO processes, respectively. The acute toxicity was evaluated by means of T spp. bioassay. It was believed that aromatic intermediates increased the toxicity and the ring-opening pathway in solar/TiO process could relieve the toxicity.

关键词： clofibric acid     advanced oxidation processes     intermediates     toxicity     Photobacterium phosphoreum T3 spp.    

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Combined process of biofiltration and ozone oxidation as an advanced treatment process for wastewater

Xinwei LI,Hanchang SHI,Kuixiao LI,Liang ZHANG

《环境科学与工程前沿（英文）》 2015年 第9卷 第6期   页码 1076-1083 doi: 10.1007/s11783-015-0770-5

摘要： The effluent of a wastewater treatment plant was treated in a pilot plant for reclaimed water production through the denitrification biofilter (DNBF) process, ozonation (O ), and biologic aerated filtration (BAF). The combined process demonstrated good removal performance of conventional pollutants, including concentrations of chemical oxygen demand (27.8 mg·L ) and total nitrogen (9.9 mg·L ) in the final effluent, which met the local discharge standards and water reuse purposes. Micropollutants (e.g., antibiotics and endocrine-disrupting chemicals) were also significantly removed during the proposed process. Ozonation exhibited high antibiotic removal efficiencies, especially for tetracycline (94%). However, micropollutant removal efficiency was negatively affected by the nitrite produced by DNBF. Acute toxicity variations of the combined process were estimated by utilizing luminescent bacteria. Inhibition rate increased from 9% to 15% during ozonation. Carbonyl compound concentrations (e.g., aldehydes and ketones) also increased by 58% as by-products, which consequently increased toxicity. However, toxicity eventually became as low as that of the influent because the by-products were effectively removed by BAF. The combined DNBF/O /BAF process is suitable for the advanced treatment of reclaimed water because it can thoroughly remove pollutants and toxicity.

关键词： wastewater treatment     micropollutant removal     ozonation     biofiltration     toxicity    

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Oxidative treatment of aqueous monochlorobenzene with thermally-activated persulfate

Qishi LUO

《环境科学与工程前沿（英文）》 2014年 第8卷 第2期   页码 188-194 doi: 10.1007/s11783-013-0544-x

摘要： The oxidation of aqueous monochlorobenzene (MCB) solutions using thermally- activated persulfate has been investigated. The influence of reaction temperature on the kinetics of MCB oxidation was examined, and the Arrenhius Equation rate constants at 20°C, 30°C, 40°C, 50°C, and 60°C for MCB oxidation performance were calculated as 0, 0.001, 0.002, 0.015, 0.057 min , which indicates that elevated temperature accelerated the rate. The most efficient molar ratio of persulfate/MCB for MCB oxidation was determined to be 200 to 1 and an increase in the rate constants suggests that the oxidation process proceeded more rapidly with increasing persulfate/MCB molar ratios. In addition, the reactivity of persulfate in contaminated water is partly influenced by the presence of background ions such as Cl , , , and . Importantly, a scavenging effect in rate constant was observed for both Cl and but not for other ions. The effective thermally activated persulfate oxidation of MCB in groundwater from a real contaminated site was achieved using both elevated reaction temperature and increased persulfate/MCB molar ratio.

关键词： persulfate     monochlorobenzene     advanced oxidation process    

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Transfer-Promoted Fe2+/Fe3+ Circulation Steered by 3D Flow-Through Co-Catalyst System Toward Sustainable AdvancedOxidation Processes

Weiyang Lv,Hao Li,Jinhui Wang,Lixin Wang,Zenglong Wu,Yuge Wang,Wenkai Song,Wenkai Cheng,Yuyuan Yao,

《工程（英文）》 doi: 10.1016/j.eng.2023.06.010

摘要： Realizing fast and continuous generation of reactive oxygen species (ROSs) via iron-based advanced oxidation processes (AOPs) is significant in the environmental and biological fields. However, current AOPs assisted by co-catalysts still suffer from the poor mass/electron transfer and non-durable promotion effect, giving rise to the sluggish Fe2+/Fe3+ cycle and low dynamic concentration of Fe2+ for ROS production. Herein, we present a three-dimensional (3D) macroscale co-catalyst functionalized with MoS2 to achieve ultra-efficient Fe2+ regeneration (equilibrium Fe2+ ratio of 82.4%) and remarkable stability (more than 20 cycles) via a circulating flow-through process. Unlike the conventional batch-type reactor, experiments and computational fluid dynamics simulations demonstrate that the optimal utilization of the 3D active area under the flow-through mode, initiated by the convection-enhanced mass/charge transfer for Fe2+ reduction and then strengthened by MoS2-induced flow rotation for sufficient reactant mixing, is crucial for oxidant activation and subsequent ROS generation. Strikingly, the flow-through co-catalytic system with superwetting capabilities can even tackle the intricate oily wastewater stabilized by different surfactants without the loss of pollutant degradation efficiency. Our findings highlight an innovative co-catalyst system design to expand the applicability of AOPs based technology, especially in large-scale complex wastewater treatment.

关键词： Advanced oxidation processes     3D co-catalyst     Flow-through mode     Enhanced mass transfer     Complex wastewater treatment    

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Oxidation and biotoxicity assessment of microcystin-LR using different AOPs based on UV, O

Siyi Lu, Naiyu Wang, Can Wang

《环境科学与工程前沿（英文）》 2018年 第12卷 第3期 doi: 10.1007/s11783-018-1030-2

摘要： Microcystin-LR attracts attention due to its high toxicity, high concentration and high frequency. The removal characteristics of UV/H O and O /H O advanced oxidation processes and their individual process for MC-LR were investigated and compared in this study. Both the removal efficiencies and rates of MC-LR as well as the biotoxicity of degradation products was analyzed. Results showed that the UV/H O process and O /H O were effective methods to remove MC-LR from water, and they two performed better than UV-, O -, H O -alone processes under the same conditions. The effects of UV intensity, H O concentration and O concentration on the removal performance were explored. The synergistic effects between UV and H O , O and H O were observed. UV dosage of 1800 mJ·cm was required to remove 90% of 100 g·L MC-LR, which amount significantly decreased to 500 mJ·cm when 1.7 mg·L H O was added. 0.25 mg·L O , or 0.125 mg·L O with 1.7 mg·L H O was needed to reach 90% removal efficiency. Furthermore, the biotoxicity results about these UV/H O , O /H O and O -alone processes all present rising trends with oxidation degree of MC-LR. Biotoxicity of solution, equivalent to 0.01 mg·L Zn , raised to 0.05 mg·L Zn after UV/H O or O /H O reaction. This phenomenon may be attributed to the aldehydes and ketones with small molecular weight generated during reaction. Advice about the selection of MC-LR removal methods in real cases was provided.

关键词： Microcystin-LR     Advanced oxidation processes (AOPs)     Biotoxicity     Synergistic effects    

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DNAN的高级氧化过程研究 Article

苏海磊, Christos Christodoulatos, Benjamin Smolinski, Per Arienti, Greg O´Connor, 孟晓光

《工程（英文）》 2019年 第5卷 第5期   页码 849-854 doi: 10.1016/j.eng.2019.08.003

摘要：

2,4-二硝基茴香醚（DNAN）是用于替代2,4,6-三硝基甲苯（TNT）的钝感炸药的一种重要成分。为了研究初始pH和过氧化氢（H2O2）剂量对DNAN降解动力学和降解途径的影响，开展了DNAN的光催化H2O2氧化实验。结果显示，初始pH为4~7且H2O2剂量为1500~4500 ppm，使用UV/ H2O2处理浓度为250 ppm的DNAN溶液时，DNAN的降解服从零级反应动力学。但是，当H2O2剂量为750 ppm时，DNAN的降解服从类一级反应动力学。结果表明，DNAN易于被UV/H2O2氧化降解。当H2O2剂量为1500 ppm且初始pH为7时，3 h内DNAN浓度从250 ppm降到1 ppm以内；但3 h内总有机碳（TOC）和总碳（TC）浓度从100 ppm降到70 ppm以下，9 h后降到5 ppm以下，说明生成了其他有机化合物。这些中间产物氧化为CO2的速度慢于DNAN的氧化速度。UV/H2O2氧化过程中，生成的CO2释放到空气中，因为溶液pH迅速降低到3左右。9 h的UV/H2O2处理后，DNAN中的N绝大多数转化为硝态氮。研究表明，UV/H2O2氧化是处理DNAN废水的有效技术。

关键词： 2     4-二硝基茴香醚     高级氧化技术     废水处理     光催化    

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Occurrence of bisphenol A in surface and drinking waters and its physicochemical removal technologies

Liping LIANG,Jing ZHANG,Pian FENG,Cong LI,Yuying HUANG,Bingzhi DONG,Lina LI,Xiaohong GUAN

《环境科学与工程前沿（英文）》 2015年 第9卷 第1期   页码 16-38 doi: 10.1007/s11783-014-0697-2

摘要： Bisphenol A (BPA), an endocrine disrupting compound, has caused wide public concerns due to its wide occurrence in environment and harmful effects. BPA has been detected in many surface waters and drinking water with the maximum concentrations up to tens of μg·L . The physicochemical technology options in eliminating BPA can be divided into four categories: oxidation, advanced oxidation, adsorption and membrane filtration. Each removal option has its own limitation and merits in removing BPA. Oxidation and advanced oxidation generally can remove BPA efficiently while they also have some drawbacks, such as high cost, the generation of a variety of transformation products that are even more toxic than the parent compound and difficult to be mineralized. Only few advanced oxidation methods have been reported to be able to mineralize BPA completely. Therefore, it is important not only to identify the major initial transformation products but also to assess their estrogenic activity relative to the parent compounds when oxidation methods are employed to remove BPA. Without formation of harmful by-products, physical separation methods such as activated carbon adsorption and membrane processes are able to remove BPA in water effluents and thus have potential as BPA removal technologies. However, the necessary regeneration of activated carbon and the low BPA removal efficiency when the membrane became saturated may limit the application of activated carbon adsorption and membrane processes for BPA removal. Hybrid processes, e.g. combining adsorption and biologic process or combining membrane and oxidation process, which can achieve simultaneous physical separation and degradation of BPA, will be highly preferred in future.

关键词： Bisphenol A (BPA)     occurrence     conventional oxidation     advanced oxidation     adsorption     membrane filtration    

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Identification of resistant pharmaceuticals in ozonation using QSAR modeling and their fate in electro-peroxone process

《环境科学与工程前沿（英文）》 2021年 第15卷 第5期 doi: 10.1007/s11783-021-1394-6

摘要：

• Effect of converting ozonation to E-peroxone was studied on pharmaceutical removal.

关键词： Ozone     Electro-peroxone     Wastewater     Quantitative structure activity relationship     Advanced oxidation processes    

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An electrochemical process that uses an Fe

Chaojie Jiang, Lifen Liu, John C. Crittenden

《环境科学与工程前沿（英文）》 2016年 第10卷 第4期 doi: 10.1007/s11783-016-0860-z

摘要： A bio-electrochemical fuel cell reactor with cathodic Fe /TiO generates electricity. It destroys recalcitrant pollutants in cathode chamber without photocatalysis. Fe /TiO generates reactive oxygenated species in the dark or under photocatalysis. Cathodic produced ROS (hydroxy radical/superoxide radical) can degrade tetracycline or dyes. Electricity generation is enhanced by semiconductor catalyzed cathodic degradation of pollutants. In this study, a new water treatment system that couples (photo-) electrochemical catalysis (PEC or EC) in a microbial fuel cell (MFC) was configured using a stainless-steel (SS) cathode coated with Fe /TiO . We examined the destruction of methylene blue (MB) and tetracycline. Fe /TiO was prepared using a chemical reduction-deposition method and coated onto an SS wire mesh (500 mesh) using a sol technique. The anode generates electricity using microbes (bio-anode). Connected via wire and ohmic resistance, the system requires a short reaction time and operates at a low cost by effectively removing 94% MB (initial concentration 20 mg·L ) and 83% TOC/TOC under visible light illumination (50 W; 1.99 mW·cm for 120 min, MFC-PEC). The removal was similar even without light irradiation (MFC-EC). The of the MFC-PEC system was approximately 0.675 kWh·m ·order , whereas that of the MFC-EC system was zero. The system was able to remove 70% COD in tetracycline solution (initial tetracycline concentration 100 mg·L ) after 120 min of visible light illumination; without light, the removal was 15% lower. The destruction of MB and tetracycline in both traditional photocatalysis and photoelectrocatalysis systems was notably low. The electron spin-resonance spectroscopy (ESR) study demonstrated that ·OH was formed under visible light, and ·O was formed without light. The bio-electricity-activated O and ROS (reactive oxidizing species) generation by Fe /TiO effectively degraded the pollutants. This cathodic degradation improved the electricity generation by accepting and consuming more electrons from the bio-anode.

关键词： Bio-anode     Photocatalytic cathode     Fe0/TiO2     ESR     Dye and antibiotics     Advanced oxidation    

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A photolysis coefficient for characterizing the response of aqueous constituents to photolysis

David R. HOKANSON,Ke LI,R. Rhodes TRUSSELL

《环境科学与工程前沿（英文）》 2016年 第10卷 第3期   页码 428-437 doi: 10.1007/s11783-015-0780-3

摘要： UV photolysis and UV based advanced oxidation processes (AOPs) are gaining more and more attention for drinking water treatment. Quantum yield ( ) and molar absorption coefficient ( ) are the two critical parameters measuring the effectiveness of photolysis of a compound. The product of the two was proposed as a fundamental measure of a constituent’s amenability to transformation by photolysis. It was shown that this product, named the photolysis coefficient, , can be determined using standard bench tests and captures the properties that govern a constituent’s transformation when exposed to light. The development showed the photolysis coefficient to be equally useful for microbiological, inorganic and organic constituents. Values of calculated by the authors based on quantum yield and molar absorption coefficient data from the literature were summarized. Photolysis coefficients among microorganisms ranged from 8500 to more than 600000 and are far higher than for inorganic and organic compounds, which varied over a range of approximately 10 to 1000 and are much less sensitive to UV photolysis than the microorganisms.

关键词： UV photolysis     disinfection     advanced oxidation     N-nitrosodimethylamine     quantum yield     absorption coefficient    

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Accelerated degradation of orange G over a widepH range in the presence of FeVO

Xiaoxia Ou, Jianfang Yan, Fengjie Zhang, Chunhua Zhang

《环境科学与工程前沿（英文）》 2018年 第12卷 第1期 doi: 10.1007/s11783-018-1013-3

摘要： In this study, FeVO was prepared andused as Fenton-like catalyst to degrade orange G (OG) dye. The removalof OG in an aqueous solution containing 0.5 g·L FeVO and 15 mmol·L hydrogen peroxide at pH 7.0 reached 93.2%. Similar rates were achievedat pH 5.7 ( = 0.0471 min ), pH 7.0 ( = 0.0438 min ), and pH 7.7 ( = 0.0434 min ). The FeVO catalyst successfullyovercomes the problem faced in the heterogeneous Fenton process, i.e.,the narrow working pH range. The data for the removal of OG in FeVO systems containing H O conform to the Langmuir–Hinshelwood model ( = 0.9988),indicating that adsorption and surface reaction are the two basicmechanisms for OG removal in the FeVO –H O system. Furthermore, the irradiationof FeVO by visible light significantly increasesthe degradation rate of OG, which is attributed to the enhanced ratesof the iron cycles and vanadium cycles.

关键词： Azo dye     Degradation     FeVO4     Kinetics     Advanced oxidation processes    

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Enhanced triallyl isocyanurate (TAIC) degradation through application of an O

Yapeng Song, Hui Gong, Jianbing Wang, Fengmin Chang, Kaijun Wang

《环境科学与工程前沿（英文）》 2020年 第14卷 第4期 doi: 10.1007/s11783-020-1243-z

摘要： Abstract • UV/O3 process had higher TAIC mineralization rate than O3 process. • Four possible degradation pathways were proposed during TAIC degradation. • pH impacted oxidation processes with pH of 9 achieving maximum efficiency. • CO32– negatively impacted TAIC degradation while HCO3– not. • Cl– can be radicals scavenger only at high concentration (over 500 mg/L Cl–). Triallyl isocyanurate (TAIC, C12H15N3O3) has featured in wastewater treatment as a refractory organic compound due to the significant production capability and negative environmental impact. TAIC degradation was enhanced when an ozone(O3)/ultraviolet(UV) process was applied compared with the application of an independent O3 process. Although 99% of TAIC could be degraded in 5 min during both processes, the O3/UV process had a 70%mineralization rate that was much higher than that of the independent O3 process (9%) in 30 min. Four possible degradation pathways were proposed based on the organic compounds of intermediate products identified during TAIC degradation through the application of independent O3 and O3/UV processes. pH impacted both the direct and indirect oxidation processes. Acidic and alkaline conditions preferred direct and indirect reactions respectively, with a pH of 9 achieving maximum Total Organic Carbon (TOC) removal. Both CO32– and HCO3– decreased TOC removal, however only CO32– negatively impacted TAIC degradation. Effects of Cl– as a radical scavenger became more marked only at high concentrations (over 500 mg/L Cl–). Particulate and suspended matter could hinder the transmission of ultraviolet light and reduce the production of HO· accordingly.

关键词： Triallyl isocyanurate     O3/UV     Advanced oxidation processes (AOP)     Degradation pathway    

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Advanced nitrogen removal by pulsed sequencing batch reactors (SBR) with real-time control

YANG Qing, PENG Yongzhen, YANG Anming, LI Jianfeng, GUO Jianhua

《环境科学与工程前沿（英文）》 2007年 第1卷 第4期   页码 488-492 doi: 10.1007/s11783-007-0078-1

摘要： The feasibility of pH and oxidation reduction potential (ORP) as on-line control parameters to advance nitrogen removal in pulsed sequencing batch reactors (SBR) was evaluated. The pulsed SBR, a novel operational mode of SBR, was

关键词： reduction potential     oxidation reduction     operational     feasibility     nitrogen    

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Decomposition of aqueous chlorinated contaminants by UV irradiation with H

Eunsung KAN,Chang-Il KOH,Kyunghyuk LEE,Joonwun KANG

《环境科学与工程前沿（英文）》 2015年 第9卷 第3期   页码 429-435 doi: 10.1007/s11783-014-0677-6

摘要： In the present study, the decomposition rates of carbon tetrachloride (CCl ) and 2,4-dichlorophenol (2,4-DCP) in water by the ultraviolet (UV) light irradiation alone and H O /UV were experimentally investigated. The detailed experimental studies have been conducted for examining treatment capacities of the two different ultraviolet light sources (low and medium pressure Hg arc) in H O /UV processes. The low or medium UV lamp alone resulted in a 60%–90% decomposition of 2,4-DCP while a slight addition of H O resulted in a drastic enhancement of the 2,4-DCP decomposition rate. The decomposition rate of 2,4-DCP with the medium pressure UV lamp alone was about 3–6 times greater than the low pressure UV lamp alone. In the direct photolysis of aqueous CCl , the medium pressure UV lamp had advantage over the low pressure UV lamp because the molar extinction coefficient of CCl at shorter wavelength (210–220 nm) is about 20 to 50 times higher than that at 254 nm. However, adding H O to the medium pressure UV lamp system rendered a negative oxidation rate because H O acted as a UV absorber being competitive with CCl due to negligible reaction between CCl and OH radicals. The results from the present study indicated significant influence of the photochemical properties of the target contaminants on the photochemical treatment characteristics for designing cost-effective UV-based degradation of toxic contaminants.

关键词： H2O2/ultraviolet (UV) light     advanced oxidation     UV light irradiation     chlorinated contaminants     photochemical treatment characteristics    

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Evaluation of the technoeconomic feasibility of electrochemical hydrogen peroxide production for decentralized water treatment

Yang Li, Yixin Zhang, Guangshen Xia, Juhong Zhan, Gang Yu, Yujue Wang

《环境科学与工程前沿（英文）》 2021年 第15卷 第1期 doi: 10.1007/s11783-020-1293-2

摘要： Abstract • Gas diffusion electrode (GDE) is a suitable setup for practical water treatment. • Electrochemical H2O2 production is an economically competitive technology. • High current efficiency of H2O2 production was obtained with GDE at 5–400 mA/cm2. • GDE maintained high stability for H2O2 production for ~1000 h. • Electro-generation of H2O2 enhances ibuprofen removal in an E-peroxone process. This study evaluated the feasibility of electrochemical hydrogen peroxide (H2O2) production with gas diffusion electrode (GDE) for decentralized water treatment. Carbon black-polytetrafluoroethylene GDEs were prepared and tested in a continuous flow electrochemical cell for H2O2 production from oxygen reduction. Results showed that because of the effective oxygen transfer in GDEs, the electrode maintained high apparent current efficiencies (ACEs,>80%) for H2O2 production over a wide current density range of 5–400 mA/cm2, and H2O2 production rates as high as ~202 mg/h/cm2 could be obtained. Long-term stability test showed that the GDE maintained high ACEs (>85%) and low energy consumption (<10 kWh/kg H2O2) for H2O2 production for 42 d (~1000 h). However, the ACEs then decreased to ~70% in the following 4 days because water flooding of GDE pores considerably impeded oxygen transport at the late stage of the trial. Based on an electrode lifetime of 46 days, the overall cost for H2O2 production was estimated to be ~0.88 $/kg H2O2, including an electricity cost of 0.61 $/kg and an electrode capital cost of 0.27 $/kg. With a 9 cm2 GDE and 40 mA/cm2 current density, ~2–4 mg/L of H2O2 could be produced on site for the electro-peroxone treatment of a 1.2 m3/d groundwater flow, which considerably enhanced ibuprofen abatement compared with ozonation alone (~43%–59% vs. 7%). These findings suggest that electrochemical H2O2 production with GDEs holds great promise for the development of compact treatment technologies for decentralized water treatment at a household and community level.

关键词： Advanced oxidation process     Electro-peroxone     Gas diffusion electrode     Hydrogen peroxide     Oxygen reduction    

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标题 作者 时间 类型 操作

Identification and ecotoxicity assessment of intermediates generated during the degradation of clofibric acid by advancedoxidation processes

Wenzhen LI, Yu DING, Qian SUI, Shuguang LU, Zhaofu QIU, Kuangfei LIN

期刊论文

Combined process of biofiltration and ozone oxidation as an advanced treatment process for wastewater

Xinwei LI,Hanchang SHI,Kuixiao LI,Liang ZHANG

期刊论文

Oxidative treatment of aqueous monochlorobenzene with thermally-activated persulfate

Qishi LUO

期刊论文

Transfer-Promoted Fe2+/Fe3+ Circulation Steered by 3D Flow-Through Co-Catalyst System Toward Sustainable AdvancedOxidation Processes

Weiyang Lv,Hao Li,Jinhui Wang,Lixin Wang,Zenglong Wu,Yuge Wang,Wenkai Song,Wenkai Cheng,Yuyuan Yao,

期刊论文

Oxidation and biotoxicity assessment of microcystin-LR using different AOPs based on UV, O

Siyi Lu, Naiyu Wang, Can Wang

期刊论文

DNAN的高级氧化过程研究

苏海磊, Christos Christodoulatos, Benjamin Smolinski, Per Arienti, Greg O´Connor, 孟晓光

期刊论文

Occurrence of bisphenol A in surface and drinking waters and its physicochemical removal technologies

Liping LIANG,Jing ZHANG,Pian FENG,Cong LI,Yuying HUANG,Bingzhi DONG,Lina LI,Xiaohong GUAN

期刊论文

Identification of resistant pharmaceuticals in ozonation using QSAR modeling and their fate in electro-peroxone process

期刊论文

An electrochemical process that uses an Fe

Chaojie Jiang, Lifen Liu, John C. Crittenden

期刊论文

A photolysis coefficient for characterizing the response of aqueous constituents to photolysis

David R. HOKANSON,Ke LI,R. Rhodes TRUSSELL

期刊论文

Accelerated degradation of orange G over a widepH range in the presence of FeVO

Xiaoxia Ou, Jianfang Yan, Fengjie Zhang, Chunhua Zhang

期刊论文

Enhanced triallyl isocyanurate (TAIC) degradation through application of an O

Yapeng Song, Hui Gong, Jianbing Wang, Fengmin Chang, Kaijun Wang

期刊论文

Advanced nitrogen removal by pulsed sequencing batch reactors (SBR) with real-time control

YANG Qing, PENG Yongzhen, YANG Anming, LI Jianfeng, GUO Jianhua

期刊论文

Decomposition of aqueous chlorinated contaminants by UV irradiation with H

Eunsung KAN,Chang-Il KOH,Kyunghyuk LEE,Joonwun KANG

期刊论文

Evaluation of the technoeconomic feasibility of electrochemical hydrogen peroxide production for decentralized water treatment

Yang Li, Yixin Zhang, Guangshen Xia, Juhong Zhan, Gang Yu, Yujue Wang

期刊论文