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2024 6th International Conference on Advanced Materials and Ecological environment, AMEE 2024

作者： Yang, Yang Zhou, Ting Du, Tianxing Dong, Wenyi Wang, Hongjie School of Civil and Environmental Engineering Harbin Institute of Technology Shenzhen Guangdong Shenzhen518055 China Shenzhen Key Laboratory of Water Resource Utilization and Environmental Pollution Control Guangdong Shenzhen518055 China State Key Laboratory of Urban Water Resource and Environment School of Environment Harbin Institute of Technology Heilongjiang Harbin150090 China

In this study, the citric acid iron and melamine was used to modify the selected biomass, preparing Fe-N/BC iron-nitrogen co-doped biochar catalyst. The BC, N/BC, and Fe-N/BC were characterized by SEM, XRD, FTIR, Raman, XPS, etc., to research the aspects of micromorphology, crystal structure, surface functional group types, and element composition. The results showed that Fe and N elements could be doped into the biochar successfully, making the particle size of Fe-N/BC smaller than that of BC, possessing a bigger surface area with a more abundant pore structure. Additionally, the graphitization degree of Fe-N/BC was enhanced, introducing active sites including pyridinic nitrogen, graphitic nitrogen, and Fe-Nx, enhancing the catalytic activity and electron transfer performance of the catalyst, enabling Fe-N/BC to simultaneously act on catalytic reduction and catalytic oxidation systems. © Published under licence by IOP Publishing Ltd.

关键词： Catalytic oxidation

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The effects of Cu-phenanthrene co-contamination on adsorption-desorption behaviors of phenanthrene in soils

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Chemosphere 2024年 349卷 140954页

作者： Li, Mengting Chen, Chuze Zhang, Wei Cao, Liu Zhang, Xueqi Wang, Yuting Xian, Qiming State Key Laboratory of Pollution Control and Resource Reuse School of Environment Nanjing University Nanjing210023 China

Polycyclic aromatic hydrocarbons (PAHs) are persistent organic pollutants in the environment, which are teratogenic, carcinogenic, and mutagenic. Co-contamination of PAHs and heavy metal commonly exists in soil. In this study, 20 types of soils with different properties in China were collected and comprehensively characterized. Phenanthrene (Phe) and Cu (II) were selected as representatives of PAHs and heavy metals, respectively. The adsorption-desorption behaviors of Phe under Phe contamination and Cu (II)-Phe co-contamination in 20 types of soils were studied. The adsorption-desorption behaviors of Phe in 20 types of soils varied greatly, and adsorption of Phe in the soils followed both linear partitioning and nonlinear surface adsorption. Soil organic matter (SOM) plays an important role in the adsorption-desorption behavior of Phe. When the concentrations of Phe were >50 μg/L, soft carbon (SC) fraction of SOM not black carbon (BC) contributed more to the adsorption of Phe. Soil dissolved organic matter (DOM), especially fulvic acid and humic acid fractions, contributes to the adsorption of Phe. Under the effect of Cu (II) (60 mg/L in solution), the adsorption capacity of soil for Phe increased, which possibly resulted from lowered pH, the existence of the cation-π bonding and the "bonding bridge" effect. The systematic investigation of adsorption-desorption behaviors of Phe in soils under heavy metal-PAHs co-contamination will provide a scientific basis for the calculation of soil environmental capacity in the future. © 2023 Elsevier Ltd

关键词： Soils

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Nano-sized Ag rather than single-atom Ag determines CO oxidation activity and stability

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Nano Research 2022年第1期15卷 452-456页

作者： Fei Wang Zhao Li Honghong Wang Min Chen Changbin Zhang Ping Ning Hong He State Key Joint Laboratory of Environment Simulation and Pollution Control Research Center for Eco-Environmental SciencesChinese Academy of SciencesBeijing 100085China Faculty of Environmental Science and Engineering Kunming University of Science and TechnologyKunming 650500China Center for Excellence in Regional Atmospheric Environment Institute of Urban EnvironmentChinese Academy of SciencesXiamen 361021China University of Chinese Academy of Sciences Beijing 100049China

Single-atom catalysis recently attracts great attentions,however,whether single atom or their nanoparticle(NP)has the advantage in its intrinsic activity remains under heated ***/Al_(2)O_(3) is a widely used catalyst for many catalytic reactions,while the effect of Ag particle size on the actity is seldom investigated due to the great difficulty in synthesizing single atom Ag and Ag clusters/particles with different ***,we firstly prepared an atomically dispersed Ag/Al_(2)O_(3) catalyst using a nano-sized y-Al_(2)O_(3) as the support,subsequently obtained a series of Ag/Al_(2)O_(3) catalysts with different Ag particle sizes by H_(2) reducing single-atom Ag/Al_(2)O_(3) catalyst at various *** Ag/Al_(2)O_(3) treated at 600℃demonstrated superior CO oxidation performance over single-atom Ag/Al_(2)O_(3) and the Ag/Al_(2)O_(3) treated at 400 and 800℃.Based on experimental data and dpnsity functional theory(DFT)calculation results,we reveal that the larger Ag°particle is beneficial to oxygen activation and improves the valence stability during oxidation reaction,while the aggregation of Ag°particle also accordingly decreases the concentration of surface active sites,hence,there is an optimum Ag0 particle *** findings clearly confirm that Ag0nanoparticle has the advantage over single-atom Ag species in its intrinsic activity for CO oxidation.

关键词： Reduction after anchoring Ag clusters single atom catalyst CO oxidation

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Dissolved black carbon mediated photo-oxidation of arsenic(III) to arsenic(V) in water: The key role of triplet states

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Chemosphere 2024年 347卷 140718页

作者： Zhou, Zhicheng Yang, Lanqing Qu, Xiaolei Fu, Heyun State Key Laboratory of Pollution Control and Resource Reuse/School of the Environment Nanjing University Jiangsu 210046 China

Arsenic is a common contaminant found in natural waters, and has raised significant environmental concerns due to its toxicity and carcinogenicity. In this study, we investigated the mediated photo-oxidation of arsenite (As(III)) under simulated sunlight by dissolved black carbon (DBC), an important dissolved organic matter (DOM) constituent released from black carbon. Five DBC were collected from the water extracts of black carbons that were derived by pyrolyzing different biomass (i.e., bamboo, rice, peanuts, corn, and sorghum stalks), and four well-studied dissolved humic substances (DHS) were selected for benchmarking. The presence of DBC (i.e., 5 mg C−1) significantly accelerated the photo-oxidation of As(III) to arsenate (As(V)), with the observed pseudo-first-order rate constant of reaction increased by 5∼11 times. Quenching experiments of photochemically produced reactive intermediates suggested that As(III) was mainly oxidized by triplet-excited DBC (3DBC*, contribution of 48%), singlet oxygen (1O2, 18%) and superoxide anions (O2•-, 28%) in sunlight-irradiated DBC solutions. The average apparent quantum yield of As(III) photo-oxidation for DBC was found to be more than 4 times higher in comparison with DHS. Such a strong mediation efficiency of DBC was due to its smaller molecular size and higher aromaticity than DHS, which facilitated the non-charge-transfer process to produce triplet-excited states and their sensitized 1O2. Consistently, DBC exhibited a higher apparent quantum yield and a longer lifetime of triplet states as compared with DHS. The results imply that DBC may play a previously unrecognized important role in the fate of arsenic in aquatic environments. © 2023 Elsevier Ltd

关键词： Excited states

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Optimized preparation of Ni-Febm bimetallic particles by ball milling NiSO4 and iron powder for efficient removal of triclosan

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Chemosphere 2024年 360卷 142359页

作者： Zhou, Bingnan Fan, Bo Gong, Zhimin Shao, Shuai Zhou, Dongmei Gao, Shixiang State Key Laboratory of Pollution Control and Resource Reuse School of the Environment Nanjing University Nanjing210023 China

The excessive usage and emissions of triclosan (TCS) pose a serious threat to aquatic environments. Iron-based bimetallic particles (Pd/Fe, Ni/Fe, and Cu/Fe, etc.) were widely used for the degradation of chlorophenol pollutants. This study proposed a novel synthesis method for the preparation of Ni/Fe bimetallic particles (Ni-Febm) by ball milling microscale zero valent iron ZVI (mZVI) and NiSO4. Ball-milling conditions such as ball-milling time, ball-milling speed and ball-to-powder ratio were optimized to prepare high activity Ni-Febm bimetallic particles. During the ball-milling process, Ni2+ was reduced to Ni0 and formed a coupled structure with ZVI. The amount of Ni0 on ZVI significantly affected the activity of Ni-Febm bimetallic particles. The highest activity Ni-Febm bimetallic particles with Ni/Fe ratio of 0.03 were synthesized under optimized conditions, which could remove 86.56% of TCS (10 μM) in aerobic aqueous solution within 60 min. In addition, higher particle dosage, lower pH condition and higher reaction temperature were more conducive for TCS degradation. The higher corrosion current and lower electron transfer impedance of Ni-Febm bimetallic particles were the main reasons for its high activity. The hydrogen atom (•H) on the surface of Ni-Febm bimetallic particles was mainly contributed to the removal of TCS, as reductive transformation products of TCS were detected by LC-TOF-MS. Notably, a small amount of oxidation products were discovered. The total dechlorination rate of TCS was calculated to be 39.67%. After eight reaction cycles, the residual Ni-Febm bimetallic particles could still degrade 28.34% of TCS within 6 h. Low Ni2+ leaching during reaction indicated that Ni-Febm bimetallic particles did not pose potential environmental risks. The prepared environmental-friendly Ni-Febm bimetallic particles with high activity have great potential in the degradation of other chlorinated organic compounds in wastewater. © 2024 Elsevier Ltd

关键词： Sulfur compounds

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Effect of nitrite on hydrolysis-acidification, biogas production and microbial community in semi-continuous two-phase anaerobic digestion of sewage sludge

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Journal of environmental Sciences 2023年第4期126卷 434-444页

作者： Qian Sheng Yiqing Lu Shijie Yuan Xiaowei Li Xiaohu Dai Yali Guo Bin Dong State Key Laboratory of Pollution Control and Resource Reuse College of Environmental Science and EngineeringTongji UniversityShanghai 200092China School of Environmental and Chemical Engineering Organic Compound Pollution Control EngineeringMinistry of EducationShanghai UniversityShanghai 200444China Shanghai Investigation Design&Research Institute Co.Ltd. Shanghai 200335China YANGTZE Eco-Environment Engineering Research Center China Three Gorges CorporationBeijing 100038China

Previous study found that the pre-treatment of sewage sludge with nitrite improves the biogas production during the mono/two-phase anaerobic digestion (AD) using batch biochemical methane potential *** this study,the effects of nitrite on hydrolysisacidification,biogas production,volatile solids destruction and microbial composition in semi-continuous two-phase AD of sewage sludge were *** addition of nitrite promotes sludge organic matter solubilization (+484%) and VFAs production (+98.9%),and causes an increase in the VS degradation rate during the AD process (+8.7%).The comparison of biogas production from the acidogenic and methanogenic reactors with or without the addition of nitrite implies that the nitrite has no significant effect on the overall biogas production of two-phase sludge AD ***-throughput sequencing analysis shows that the microbial communities of bacteria and archaea in two-phase AD reactors significantly changes after the addition of *** (bacteria) and Candidatus Methanofastidiosum (archaea) become the dominant genera in the acidogenic and methanogenic reactors with the nitrite *** findings provide new insights about using nitrite to promote the organic matter degradation of sewage sludge in a semicontinuous two-phase AD system.

关键词： Sewage sludge Bioenergy Methane production Nitrite Semi-continuous two-phase anaerobic digestion

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Effect of sulfate on Cu(Ⅱ)sorption to polymer-supported nano-hydrated ferric oxides:Experimental and modeling studies

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Chinese Journal of Chemical Engineering 2021年第5期34卷 319-326页

作者： Wenxiang Ni Luyang Yang Xiaolin Zhang Hui Qiu Collaborative Innovation Center of Atmospheric Environment and Equipment Technology Jiangsu Key Laboratory of Atmospheric Environment Monitoring and PollutionControlSchool of Environmental Science and EngineeringNanjing University of Information Science&TechnologyNanjing 210044China State Key Laboratory of Pollution Control and Resource Reuse School of the EnvironmentNanjing UniversityNanjing 210023China

Incorporating of hydrous ferric oxide(HFO)inside porous supports with large sizes has become an effective way to decontaminate the water from heavy *** anions like sulfate are usually present in high concentrations in water,and might greatly affect adsorption behavior of hybrid ***,a polymer-based HFO-CPS was fabricated by encapsulating nano-HFO inside a chloromethylated polystyrene polymer(CPS)and the reactivity of HFO-CPS with Cu(Ⅱ)was evaluated in the presence of sulfate *** complexation theory was firstly employed to describe the effect of sulfate on Cu(Ⅱ)adsorption edges of hybrid HFO-CPS,where constant capacitance model(CCM)was *** available weak adsorption site Fe_((2))OH of hybrid HFO-CPS was found to decrease from 20% Fe to 5% Fe,which might be caused by the pore plugging effect after HFO *** the assumption that a ternary complex was formed,the effect of sulfate on Cu(Ⅱ)adsorption by HFO-CPS were successfully described by CCM using the optimized Fe_((2))OH site under different sulfate concentrations(1 or 10 mmol·L^(-1))and Cu/Fe ratios(0.0042 or 0.0252).It is confirmed that the formation of FeOHCuSO4 ternary surface complexes played an important role in enhancing Cu(Ⅱ)adsorption on HFO-CPS in the presence of sulfate.

关键词： Iron oxides Polymer Sulfate Adsorption Ternary complex

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Enhanced performance of photocatalytic oxidation of indoor toluene over Pd/TiO2 catalyst by tuning surface defect concentrations

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Chemosphere 2024年 366卷 143409页

作者： Wang, Gehui Wu, Cong Liu, Qinglong Wan, Haiqin Dong, Lin State Key Laboratory of Pollution Control and Resource Reuse School of Environment Nanjing University Nanjing210023 China

An effective approach for the elimination of indoor gaseous toluene through photocatalytic oxidation involves the engineering of surface defects on catalysts. In this study, the concentrations of surface oxygen defects in PdTi-xN (x = 10, 30) catalysts were controlled using the sodium borohydride solid-phase reduction method, and their performances in the photocatalytic oxidation of indoor gaseous toluene were evaluated. PdTi–10 N demonstrated high photocatalytic efficiency for toluene oxidation, achieving 84% toluene conversion and approximately 75% CO2 mineralization. Characterization results indicated that surface oxygen defects can enhance the separation of photo-generated electrons and holes, facilitating their interaction with Pd0 species to form Ti3+ species. More reactive oxygen species (·OH-and ·O2−) were generated on PdTi–10 N due to the synergistic effect of surface oxygen defect and Ti3+ species, which played a significant role as the toluene oxidation. This work provides a new insight for the design and development of high-performance Pd/TiO2 catalysts in the field of indoor VOCs treatment. © 2024 Elsevier Ltd

关键词： Toluene

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Climate change projections for Diamer Division in lesser Himalayas using multi-global climate model ensemble

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environmental Science and pollution Research 2025年第3期32卷 1668-1680页

作者： Ahmad, Didar Faridullah, Faridullah Irshad, Muhammad Bacha, Aziz Ur Rahim Hafeez, Farhan Iqbal, Akhtar Ullah, Zahid Afridi, Muhammad Naveed Alrefaei, Abdulwahed Fahad Nazir, Rashid Department of Environmental Sciences COMSATS University Islamabad Abbottabad Campus Abbottabad22060 Pakistan State Key Laboratory of Urban Water Resource and Environment Shenzhen Key Laboratory of Organic Pollution Prevention and Control School of Eco-Environment Harbin Institute of Technology Shenzhen Shenzhen518055 China Department of Environmental Science and Engineering Fudan University Shanghai200433 China State Key Laboratory of Biogeology and Environmental Geology School of Environmental Studies China University of Geosciences Wuhan430074 China Department of Zoology College of Science King Saud University P.O. Box 2455 Riyadh11451 Saudi Arabia

Pakistan, like many other regions around the world, is experiencing the impacts of climate change, particularly in its northern region. These changes have adverse impacts on ecosystems and biodiversity. Herein, we have investigated future projections of temperature and precipitation trends for three periods historical (HT = 1975–2005), near-term (NT = 2010–2029), and mid-term (MT = 2030–2050) using climate model intercomparison projects along with global climate models (GCMs) including RCP4.5 and RCP8.5. The historical records spanning from 1975 to 2005 reveal that the Chilas region has a notable rise of 8 °C in maximum temperature (Tmax), whereas the Astore district exhibited a trend of decreasing temperatures. When examining the projected temperature trends using GCMs (RCP4.5 and RCP8.5), the Chilas region is predicted to undergo a further increase of 6 °C in Tmax. In contrast, the Babusar region is projected to observe a significant decrease of 2 °C for the period between 2010 and 2050. Additionally, the precipitation results obtained from historical-based analysis for the period 1975 to 2005 indicated that the Babusar area exhibited increased precipitation patterns to 20 mm on an annual basis. Similarly, the Astore region has the most significant decline in precipitation, with a reduction of 40 mm annually. The predicted precipitation patterns for the period between 2010 and 2050 under the RCP8.5 revealed that the Babusar region has maximum precipitation (25 mm). Conversely, the Astore region exhibited reduced precipitation patterns, recording minimum precipitation (40 mm). In the results from RCP4.5, the precipitation showed a similar pattern with a maximum of 35 mm and a minimum of 15 mm in the Babusar and Astore, respectively. The region’s glaciers, snow cover, and land use systems are deteriorated by these changes in temperature and precipitation patterns. The increased winter and decreased summer precipitation under varied temperatures and precipitation cau

关键词： Miocene

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Organic peroxyl radicals from biacetyl accelerated the visible-light degradation of steroid estrogens in aqueous solution

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Chemosphere 2024年 351卷 141195页

作者： Jia, Yulu Zhang, Chengyang Zheng, Hongcen Zhang, Guoyang Zhang, Shujuan State Key Laboratory of Pollution Control and Resource Reuse School of Environment Nanjing University Nanjing210023 China

Indirect photodegradation is an important pathway for the reduction of steroid estrogens in sunlit surface waters. Nevertheless, the kinetics and mechanisms governing the interaction between coexisting carbonyl compounds and estrogens under visible light (Vis) remain unexplored. This study systematically investigates the Vis-induced photodegradation of 17β-estradiol (E2) in the presence of five specific carbonyl compounds—biacetyl (BD), acetone, glyoxal, pyruvic acid, and benzoquinone. The results demonstrate that, among these compounds, only BD significantly enhanced the photodegradation of E2 under Vis irradiation (λ > 400 nm). The pseudo-first order photodegradation rate constants (k1) of E2 in the Vis/BD system were 0.025 min−1 and 0.076 min−1 in ultrapure water and river water, respectively. The enhancing effect of BD was found to be pH-dependent, increasing the pH from 3.0 to 11.0 resulted in a 76% reduction in the k1 value of E2 in the Vis/BD system. Furthermore, the presence of humic acid, NO3−, or HCO3− led to an increase of more than 35% in the k1 value of E2, while NO2− exerted a pronounced inhibitory effect, resulting in a 92% decrease. Peroxyacetyl and peroxymethyl radicals, derived from BD in a yield ratio of 9, played a crucial role in the degradation of E2. These peroxyl radicals primarily targeted electron-rich hydroxyl sites of E2, initiating hydroxylation and ring-opening reactions that culminated in the formation of acidic byproducts. Notably, toxicity evaluation indicates that these hydroxylated and acidic products exhibited lower toxicity than the parent compound E2. This study highlights the important role of peroxyl radicals in estrogen degradation within aquatic environment, and also helps to design efficient visible light-responsive photo-activators for the treatment of estrogen-contaminated waters. © 2024 Elsevier Ltd

关键词： Photolysis

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