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Low-temperature plasma induced phosphate groups onto coffee residue-derived porous carbon for efficient U(Ⅵ) extraction

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Journal of Environmental Sciences 2022年第12期34卷 1-13页

作者： Zhongshan Chen Xuan He Qian Li Hui Yang Yang Liu Lining Wu Zhixin Liu Baowei Hu Xiangke Wang School of Life Science Shaoxing UniversityShaoxing 312000China College of Environmental Science and Engineering North China Electric Power UniversityBeijing 102206China School of Energy Power and Mechanical Engineering North China Electric Power UniversityBeijing 102206Chin

For the continuous utilization of nuclear energy and efficient control of radioactive pollution, low-cost materials with high efficient U(VI) removal are of great importance. In this study, low temperature plasma method was applied for the successful modification of Ophosphorylethanolamine(O-PEA) on the porous carbon materials. The produced materials(Cafe/O-PEA) could adsorb U(VI) efficiently with the maximum sorption capacity of 648.54mg/g at 1 hr, T=298 K, and p H=6.0, much higher than those of most carbon-based composites. U(VI) sorption was mainly controlled by strong surface complexation. From FTIR,SEM-EDS and XPS analyses, the sorption of U(VI) was related to the complexation with-NH2, phosphate and-OH groups on Cafe/O-PEA. The low temperature plasma method was an efficient, environmentally friendly and low-cost method for surface modification of materials for the effective enrichment of U(VI) from aqueous solutions.

关键词： U(Ⅵ) Coffee residue porous carbon Low-temperature plasma modification

porous carbon framework nested nickel foam as freestanding host for high energy lithium sulfur batteries

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Chinese Chemical Letters 2021年第3期32卷 1106-1110页

作者： Yan Song Xiuyuan Li Chaozheng He Shaanxi Key Laboratory of Optoelectronic Functional Materials and Devices School of Materials Science and Chemical EngineeringXi’an Technological UniversityXi’an 710021China Institute of Environmental and Energy Catalysis School of Materials Science and Chemical EngineeringXi'an Technological UniversityXi'an 710021China

Constructing 3 D multifunctional conductive framework as stable sulfur cathode contributes to develop advanced lithium-sulfur(Li-S)batteries.Herein,a freestanding electrode with nickel foam framework and nitrogen doped porous carbon(PC)network is presented to encapsulate active sulfur for Li-S batteries.In such a mutually embedded architecture with high stability,the interconnected carbon network and nickel foam matrix can expedite ionic/electro nic tra nsport and sustain volume variations of sulfur.Furthermore,rationally designed porous structures provide sufficient internal space and large surface area for high active sulfur loading and polar polysulfides anchoring.Benefiting from the synergistic superiority,the Ni/PC-S cathode exhibits a high initial capacity of around 1200 mAh/g at 0.2 C,excelle nt rate perfo rmance,and high cycling stability with a low decay rate of 0.059%per cycle after 500 cycles.This work provides a useful strategy to exploit freestanding porous framework for diverse applications.

关键词： porous carbon Nitrogen doping Polysulfides anchoring Freestanding electrode Lithium-sulfur batteries

Highly sensitive electrochemical determination of rutin based on the synergistic effect of 3D porous carbon and cobalt tungstate nanosheets

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Journal of Pharmaceutical Analysis 2022年第3期12卷 453-459页

作者： Guangjun Feng Yang Yang Jiantao Zeng Jun Zhu Jingjian Liu Lun Wu Zhiming Yang Guanyi Yang Quanxi Mei Qinhua Chen Fengying Ran Shenzhen Baoan Authentic TCM Therapy Hospital Shenzhen518101China Sinopharm Dongfeng General Hospital Hubei University of MedicineShiyanHubei442008China Shenzhen Hospital of Integrated Traditional Chinese and Western Medicine Shenzhen518101China

Rutin,a flavonoid found in fruits and vegetables,is a potential anticancer compound with strong anticancer activity.Therefore,electrochemical sensor was developed for the detection of rutin.In this study,CoWO_(4) nanosheets were synthesized via a hydrothermal method,and porous carbon(PC)was prepared via high-temperature pyrolysis.Successful preparation of the materials was confirmed,and characterization was performed by transmission electron microscopy,scanning electron microscopy,and X-ray photoelectron spectroscopy.A mixture of PC and CoWO_(4) nanosheets was used as an electrode modifier to fabricate the electrochemical sensor for the electrochemical determination of rutin.The 3D CoWO_(4) nanosheets exhibited high electrocatalytic activity and good stability.PC has a high surface-to-volume ratio and superior conductivity.Moreover,the hydrophobicity of PC allows large amounts of rutin to be adsorbed,thereby increasing the concentration of rutin at the electrode surface.Owing to the synergistic effect of the 3D CoWO_(4) nanosheets and PC,the developed electrochemical sensor was employed to quantitively determine rutin with high stability and sensitivity.The sensor showed a good linear range(5-5000 ng/mL)with a detection limit of 0.45 ng/mL.The developed sensor was successfully applied to the determination of rutin in crushed tablets and human serum samples.

关键词： Rutin Electrochemical detection CoWO_(4)nanosheets porous carbon Sensor

Boron-doped lamellar porous carbon supported copper catalyst for dimethyl oxalate hydrogenation

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Chinese Journal of Chemical Engineering 2023年第3期55卷 222-229页

作者： Peipei Ai Li Zhang Jinchi Niu Huiqing Jin Wei Huang State Key Laboratory of Clean and Efficient Coal Utilization Taiyuan University of TechnologyTaiyuan 030024China

Doping heteroatoms on carbon materials could bring some special advantages for using as catalyst support.In this work, a boron doped lamellar porous carbon(B-LPC) was prepared facilely and utilized as carbonbased support to construct Cu/B-LPC catalyst for dimethyl oxalate(DMO) hydrogenation. Doping boron could make the B-LPC own more defects on surface and bigger pore size than B-free LPC, which were beneficial to disperse and anchor Cu nanoparticles. Moreover, the interaction between Cu species and B-LPC could be strengthened by the doped B, which not only stabilized the Cu nanoparticles, but also tuned the valence of Cu species to maintain more Cu^(+). Therefore, the B-doped Cu/B-LPC catalyst exhibited stronger hydrogenation ability and obtained higher alcohols selectivity than Cu/LPC, as well as high stability without decrease of DMO conversion and ethylene glycol selectivity even after 300 h of reaction at 240℃.

关键词： Hydrogenation Cu-based catalyst Boron doping porous carbon Catalyst support Alcohol

FeMo@porous carbon derived from MIL-53(Fe)@MoO_(3) as excellent heterogeneous electro-Fenton catalyst: Co-catalysis of Mo

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Journal of Environmental Sciences 2023年第5期127卷 652-666页

作者： Xuedong Du Wenyang Fu Pei Su Qizhan Zhang Minghua Zhou Key Laboratory of Pollution Process and Environmental Criteria Ministry of EducationCollege of Environmental Science and EngineeringNankai UniversityTianjin 300350China Tianjin Key Laboratory of Environmental Technology for Complex Trans-Media Pollution Nankai UniversityTianjin 300350China Tianjin Advanced Water Treatment Technology International Joint Research Center College of Environmental Science and EngineeringNankai UniversityTianjin 300350China

An ultra-efficient electro-Fenton catalyst with porous carbon coated Fe-Mo metal(FeMo@PC),was prepared by calcining MIL-53(Fe)@MoO_(3).This FeMo@PC-2 exhibited impressive catalytic performance for sulfamethazine(SMT)degradation with a high turnover frequency value(7.89 L/(g·min)),much better than most of reported catalysts.The mineralization current efficiency and electric energy consumption were 83.2%and 0.03 kWh/gTOC,respectively,at lowcurrent(5mA)and small dosage of catalyst(25.0mg/L).The removal rate of heterogeneous electro-Fenton(Hetero-EF)process catalyzed by FeMo@PC-2 was 4.58 times that of Fe@PC/Hetero-EF process.Because the internal-micro-electrolysis occurred between PC and Fe0,while the co-catalysis of Mo accelerated the rate-limiting step of the Fe^(3+)/Fe^(2+) cycle and greatly improved the H_(2)O_(2)utilization efficiency.The results of radical scavenger experiments and electron paramagnetic resonance confirmed the main role of surface-bound hydroxyl radical oxidation.This process was feasible to remove diverse organic contaminants such as phenol,2,4-dichlorophenoxyacetic acid,carbamazepine and SMT.This paper enlightened the importance of the doped Mo,which could greatly improve the activity of the iron-carbon heterogeneous catalyst derived from metal-organic frameworks in EF process for efficient removal of organic contaminants.

关键词： Metal-organic frameworks derivatives Fe-Mo bimetal porous carbon Co-catalysis Heterogeneous electro-Fenton

One-pot green mass production of hierarchically porous carbon via a recyclable salt-templating strategy

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Green Energy & Environment 2022年第4期7卷 818-828页

作者： Changde Ma Jiang Gong Shuang Zhao Xiaoguang Liu Xueying Mu Yanhui Wang Xuecheng Chen Tao Tang State Key Laboratory of Polymer Physics and Chemistry Changchun Institute of Applied ChemistryChinese Academy of SciencesChangchun130022China University of Science and Technology of China Hefei230026China Key Laboratory for Material Chemistry of Energy Conversion and Storage Ministry of EducationSchool of Chemistry and Chemical EngineeringHuazhong University of Science and TechnologyWuhanChina Faculty of Chemical Technology and Engineering West Pomeranian University of TechnologyPiastow Ave.42Szczecin71-065Poland

porous carbon materials have exhibited a series of promising applications in supercapacitors and other research fields,yet still confronting the complicated synthetic procedures and massive usage of toxic reagents.Herein,we propose a green and one-pot method to produce heteroatomdoped hierarchical porous carbon materials in large-scale without any toxic reagents employed.Eventually,the as-prepared nitrogen-doped porous carbon(NPC)displays a high specific surface area of 2018 m^(2)g^(-1)together with abundant heteroatom dopants(14.8 wt%O and 1.03 wt%N).The potassium carbonate template can be recycled via a simple rinsing and re-precipitation process.Furthermore,the as-prepared nitrogen-doped porous carbon delivers a high specific capacitance of 361 F g^(-1)at 0.5 A g^(-1)and excellent rate capability of 240 F g^(-1)at 20 A g^(-1)(66.5%capacitance retention).Finally,considering the low-price raw materials and facile green synthesis procedure,the present approach can be easily scalable to prepare biomass-derived heteroatoms doped porous carbon,which is not only applicable for supercapacitor but also for other research fields.

关键词： porous carbon Supercapacitors Green Salt template Recyclable

Boron and nitrogen co-doped porous carbon derived from sodium alginate enhanced capacitive deionization for water purification

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Frontiers of Chemical Science and Engineering 2023年第12期17卷 2014-2024页

作者： Xiao Yong Pengfei Sha Jinghui Peng Mengdi Liu Qian Zhang Jianhua Yu Liyan Yu Lifeng Dong College of Materials Science and Engineering Qingdao University of Science and TechnologyQingdao 266042China Department of Physics Hamline UniversitySaint PaulMN 55104USA

Capacitive deionization can alleviate water shortage and water environmental pollution, but performances are greatly determined by the electrochemical and desalination properties of its electrode materials. In this work, B and N co-doped porous carbon with micro-mesoporous structures is derived from sodium alginate by a carbonization, activation, and hydrothermal doping process, which exhibits large specific surface area (2587 m^(2)·g^(‒1)) and high specific capacitance (190.7 F·g^(‒1)) for adsorption of salt ions and heavy metal ions. Furthermore, the materials provide a desalination capacity of 26.9 mg·g−1 at 1.2 V in 500 mg·L^(‒1) NaCl solution as well as a high removal capacity (239.6 mg·g^(‒1)) and adsorption rate (7.99 mg·g^(‒1)·min^(‒1)) for Pb2+ with an excellent cycle stability. This work can pave the way to design low-cost porous carbon with high-performances for removal of salt ions and heavy metal ions.

关键词： capacitance deionization porous carbon B N co-doping heavy metal ions water purification

Synthesis of porous carbon from orange peel waste for effective volatile organic compounds adsorption: role of typical components

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Frontiers of Chemical Science and Engineering 2023年第7期17卷 942-953页

作者： Qiaoyan Zhou Huan Liu Yipeng Wang Kangxin Xiao Guangyan Yang Hong Yao School of Energy and Power Engineering Huazhong University of Science and TechnologyWuhan 430074China Research Institute of Huazhong University of Science and Technology in Shenzhen Shenzhen 518000China Universtar Science&Technology(Shenzhen)Co. Ltd.Shenzhen 518057China

Volatile organic compounds have posed a serious threat to the environment and human health,which require urgent and effective removal.In recent years,the preparation of porous carbon from biomass waste for volatile organic compounds adsorption has attracted increasing attention as a very cost-effective and promising technology.In this study,porous carbon was synthesized from orange peel by urea-assisted hydrothermal carbonization and KOH activation.The role of typical components(cellulose,hemicellulose,and lignin)in pore development and volatile organic compounds adsorption was investigated.Among the three components,hemicellulose was the major contributor to high porosity and abundant micropores in porous carbon.Higher hemicellulose content led to more abundant–COOR,amine-N,and pyrrolic/pyridonic-N in the derived hydrochar,which were favorable for porosity formation during activation.In this case,the toluene adsorption capacity of the porous carbon improved from 382.8 to 485.3 mg·g^(–1).Unlike hemicellulose,cellulose reduced the>C=O,amine-N,and pyrrolic/pyridonic-N content of the hydrochar,which caused porosity deterioration and worse toluene adsorption performance.Lignin bestowed the hydrochar with slightly increased–COOR,pyrrolic/pyridonic-N,and graphitic-N,and reduced>C=O,resulting in comparatively poor porosity and more abundant micropores.In general,the obtained porous carbon possessed abundant micropores and high specific surface area,with the highest up to 2882 m^(2)·g^(–1).This study can provide guidance for selecting suitable biomass waste to synthesize porous carbon with better porosity for efficient volatile organic compounds adsorption.

关键词： biomass waste porous carbon feedstock composition urea-assisted hydrothermal carbonization toluene adsorption N-doped hydrochar

Biomass seaweed-derived n itrogen self-doped porous carb on anodes for sodium-ion batteries:Insights into the structure and electrochemical activity

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Journal of Energy Chemistry 2022年第1期31卷 286-295,I0008页

作者： Chenrayan Senthil Jae Woo Park Nitheesha Shaji Gyu Sang Sim Chang Woo Lee Department of Chemical Engineering(Integrated Engineering)&Center for the SMART Energy Platform College of EngineeringKyung Hee University1732 Deogyeong-daeroCihuengYonginGyeonggi 17104South Korea

Sustainable transformation and efficient utilization of biomasses and their derived materials are environ-mentally as well as economically compliant strategies.Biomass seaweed-derived nitrogen self-doped porous carbon with tailored surface area and pore structures are prepared through carb on izatio n and activation.The in fluence of carb on ization temperature on morphology,surface area,and heteroatom dopants are investigated to optimize sodium-ion storage capability.Seaweed-derived nitrogen selfdoped activated carbon(SAC)as anode materials for sodium-ion batteries exhibits remarkable reversible capacity of 303/192 mAh g^(-1) after 100/500 cycles at current densities of 100/200 mA g^(-1) respectively,and a good rate capability.The interconnected and porous conducting nature along with the heteroatom dopant role in creating defective sites and charge stabilization are favorable for ion storage and diffusion and electron transport,indicating the electrodes can offer improved electrochemical performances.In addition,post-mortem analysis of the cycled carbon electrodes through ex-situ tools demonstrates the sodium-ion storage mechanism.

关键词： Biomass Heteroatom self-doping porous carbon Anode Sodium-ion batteries Post-mortem ex-situ analysis