| 1. |
- Wang, Hongyu, et al.
(författare)
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Exploration of selective copper ion separation from wastewater via capacitive deionization with highly effective 3D carbon framework-anchored Co(PO3)2 electrode
- 2024
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Ingår i: Separation and Purification Technology. - : ELSEVIER. - 1383-5866 .- 1873-3794. ; 336
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Tidskriftsartikel (refereegranskat)abstract
- The increasing amount of heavy metal copper ions (Cu2+) in industrial emissions, poses a serious threat to human health, biological environment, and resource scarcity. Capacitive deionization (CDI) is considered as a green and efficient method for desalination. It is crucial to develop high-performance electrodes for efficient operation of CDI that go beyond conventional carbon and yield considerable environmental benefits. Here, metal organic frameworks (MOFs) derived carbon-loaded cobalt metaphosphate (NC-Co(PO3)2) was prepared by lowtemperature gas-solid phosphating for Cu2+ removal as CDI electrode for the first time. NC-Co(PO3)2 demonstrated superior electrode structure and function due to the synergistic effects of electric double layer coupling PO bonds, the binding tendency of metaphosphate groups with Cu2+, and interfacial redox reactions induced by the labile valence state of cobalt. The optimal electrosorption capacity of NC-Co(PO3)2 was 95.41 mg g-1 at 1 V in 50 mL Cu2+ solution with splendid cyclic regeneration capability. Moreover, NC-Co(PO3)2 exhibited excellent selectivity and outstanding electrosorption performance in the presence of multiple coexisting ions and this CDI system realized the purification of actual copper-containing wastewater. A series of characterizations further revealed the specific mechanism of Cu2+ in adsorption-desorption process. Our finding strongly supported NCCo(PO3)2 electrode can extend the CDI platform's capability for effectively removing and retrieving Cu2+ from wastewater.
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| 2. |
- Zhang, Hongguo, et al.
(författare)
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Cu-doped CaFeO3 perovskite oxide as oxygen reduction catalyst in air cathode microbial fuel cells
- 2022
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Ingår i: Environmental Research. - : ACADEMIC PRESS INC ELSEVIER SCIENCE. - 0013-9351 .- 1096-0953. ; 214
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Tidskriftsartikel (refereegranskat)abstract
- Cathode electrocatalyst is quite critical to realize the application of microbial fuel cells (MFCs). Perovskite oxides have been considered as potential MFCs cathode catalysts to replace Pt/C. Herein, Cu-doped perovskite oxide with a stable porous structure and excellent conductivity was successfully prepared through a sol-gel method. Due to the incorporation of Cu, CaFe0.9Cu0.1O3 has more micropores and a larger surface area, which are more conducive to contact with oxygen. Doping Cu resulted in more Fe3+ in B-site and thus enhanced its binding capability to oxygen molecules. The data from electrochemical test demonstrated that the as-prepared catalyst has good conductivity, high stability, and excellent ORR properties. Compared with Pt/C catalyst, CaFe0.9Cu0.1O3 exhibits a lower overpotential, which had an onset potential of 0.195 V and a half-wave potential of 0.224 V, respectively. CaFe0.9Cu0.1O3 displays an outstanding four-electron pathway for ORR mechanism and demonstrates superiors corrosion resistance and stability. The MFC with CaFe0.9Cu0.1O3 has a greater maximum power density (1090 mW m(-3)) rather than that of Pt/C cathode (970 mW m(-3)). This work demonstrated CaFe0.9Cu0.1O3 is an economic and efficient cathodic catalyst for MFCs.
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| 3. |
- Dai, Junxi, et al.
(författare)
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Promoted Sb removal with hydrogen production in microbial electrolysis cell by ZIF-67-derived modified sulfate-reducing bacteria bio-cathode
- 2023
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Ingår i: Science of the Total Environment. - : ELSEVIER. - 0048-9697 .- 1879-1026. ; 856
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Tidskriftsartikel (refereegranskat)abstract
- Bio-cathode Microbial electrolysis cell (MEC) has been widely discovered for heavy metals removal and hydrogen production. However, low electron transfer efficiency and heavy metal toxicity limit MEC treatment efficiency. In this study, ZIF-67 was introduced to modify Sulfate-reducing bacteria (SRB) bio-cathode to enhance the bioreduction of sulfate and Antimony (Sb) with hydrogen production in the MEC. ZIF-67 modified bio-cathode was developed from a bio-anode microbial fuel cell (MFC) by operating with an applied voltage of 0.8 V to reverse the polarity. Cyclic voltammetry, linear sweep voltammetry and electrochemical impedance were done to confirm the performance of the ZIF67 modified SRB bio-cathode. The synergy reduction of sulfate and Sb was accomplished by sulfide metal precipitation reaction from SRB itself. Maximum sulfate reduction rate approached 93.37 % and Sb removal efficiency could reach 92 %, which relies on the amount of sulfide concentration generated by sulfate reduction reaction, with 0.923 +/- 0.04 m(3) H-2/m(3) of hydrogen before adding Sb and 0.857 m(3) H-2/m(3) of hydrogen after adding Sb. The hydrogen was mainly produced in this system and the result of gas chromatography (GC) indicated that 73.27 % of hydrogen was produced. Meanwhile the precipitates were analyzed by X-ray diffraction and X-ray photoelectron spectroscopy to confirm Sb2S3 was generated from Sb (V).
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| 4. |
- Dai, Yi, et al.
(författare)
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Zn-doped CaFeO3 perovskite-derived high performed catalyst on oxygen reduction reaction in microbial fuel cells
- 2021
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Ingår i: Journal of Power Sources. - : ELSEVIER. - 0378-7753 .- 1873-2755. ; 489
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Tidskriftsartikel (refereegranskat)abstract
- Stable perovskite oxide is considered as a potential cathode for microbial fuel cells (MFCs). Herein, Zn is used as an effective element to modify the micro-structure and oxygen vacancy of perovskite to be a novel cathode catalyst. Physical characterizations show that due to partial volatilization at high temperature of Zn, perovskite forms hierarchically porous structures. Moreover, Zn is precipitated in electrochemical reaction to generate Zn vacancy in situ; thus, the active center of Fe has a superior interaction with oxygen-containing species, promoting the production of oxygen vacancy and forms a mixed valence state of Fe2+/Fe3+. The Zn-doped perovskite material CaFe0.7Zn0.3O3 exhibits remarkable oxygen reduction reaction (ORR) performances with outstanding onset potential (0.194 V vs. Ag/AgCl) and half-wave potential (-0.219 V vs. Ag/AgCl) under alkaline condition, which is better than Pt/C catalyst. Besides, CaFe0.7Zn0.3O3 shows an excellent four-electron pathway of ORR mechanism with remarkable corrosion resistance and stability, which enables a more reliable cathode electrocatalyst. The maximum power density of CaFe0.7Zn0.3O3 (892.10 +/- 90.79 mW m(-3)) testing on microbial fuel cell is comparable to the maximum power density (1012.86 +/- 84.03 mW m(-3)) of Pt/C. The findings of this work provide the feasibility of exploring inexpensive and high-performance cathode catalyst.
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| 5. |
- Huang, Linzhe, et al.
(författare)
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Facile synthesis of hollow carbon spheres by gas-steamed bifunctional NH4F for efficient cathodes in microbial fuel cells
- 2023
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Ingår i: Carbon. - : PERGAMON-ELSEVIER SCIENCE LTD. - 0008-6223 .- 1873-3891. ; 207, s. 86-94
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Tidskriftsartikel (refereegranskat)abstract
- A facile gas-steamed strategy is reported for preparing heteroatom dual-doped hierarchical porous hollow carbon catalysts via carbonization of a mixture of carbon sphere precursor and ammonium fluoride (NH4F). Notably, NH4F can be decomposed into NH3 and HF by pyrolysis, in which HF gas can etch SiO2 pellets to form hollow structure while the N and F atoms can be introduced at the same time. The FCS-900 exhibits admirable elec-trocatalytic properties with the highest onset potential and limiting current density in neutral electrolytes (0.944 V vs. RHE and 6.44 mA cm-2). In comparison to MFC-Pt, much higher output voltage and power density (0.617 V and 1093.6 +/- 6.26 mW m-2) are obtained by MFC-900. Such results can be attributed to the largest specific surface area of FCS-900 to supply exposed active sites and fast transportation channels. Based on X-ray photo-electron spectroscopy, the FCS-900 catalyst possesses the active substances of pyridinic/graphitic N and C-F bonds. The synergism of N and F can effectively facilitate the adsorption of O2 during ORR, as further supported by density functional theory calculation. The facile and green synthesis strategy can be extended to design metal -free carbon-based electrocatalysts with superior electrocatalytic performance.
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| 6. |
- Huang, Linzhe, et al.
(författare)
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Facile synthesis of NS@UiO-66 porous carbon for efficient oxygen reduction reaction in microbial fuel cells
- 2022
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Ingår i: Journal of Power Sources. - : ELSEVIER. - 0378-7753 .- 1873-2755. ; 544
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Tidskriftsartikel (refereegranskat)abstract
- Exploiting a facile way to synthesize low-cost and high-performance oxygen reduction reaction (ORR) catalysts is a core issue in microbial fuel cells (MFCs). Hence, a facile and extensible method has been developed to prepare efficient ORR catalysts by using robust UiO-66 as a precursor, modified with melamine and trithiocyanuric via the impregnation method. Benefiting from the hierarchical structure of UiO-66, the NS@UiO-66 has excellent stability, more active sites and improved mass transfer. Significantly, the half-wave potential and the current density of the NS@UiO-66 are 0.546 V vs. RHE and 6.19 mA cm(-2) respectively, which is better than that of benchmark Pt/C in neutral conditions. Furthermore, the power density of MFCs assembled with the NS@UiO-66 catalyst is 318.6 +/- 2.15 mW m(-2). The density functional theory calculation demonstrates that the reaction barrier can be reduced effectively for accelerating the ORR process through the synergistic effect of N and S. The NS@UiO-66, as an ideal candidate to substitute for the commercial Pt/C counterpart, is expected to promote the scaling-up production and application of MFCs due to low-cost elements doping and facilely synthetic method.
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| 7. |
- Li, Han, et al.
(författare)
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A co-doped oxygen reduction catalyst with FeCu promotes the stability of microbial fuel cells
- 2022
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Ingår i: Journal of Colloid and Interface Science. - : ACADEMIC PRESS INC ELSEVIER SCIENCE. - 0021-9797 .- 1095-7103. ; 628, s. 652-662
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Tidskriftsartikel (refereegranskat)abstract
- Air cathode microbial fuel cell (AC-MFC) cannot be used on a large scale because of its low oxygen reduction reaction (ORR) efficiency. Despite the fact that bimetallic catalysts can greatly enhance the oxygen reduction rate by regulating the electronic structure of the active site, the flaws of insufficient exposure of the active site and easy metal agglomeration limit its catalytic activity. Herein, we report on the preparation of a stable heteroatomic substrate using a copper material organic framework as a precursor, covered by Fe-based active sites. As a result of dipole-dipole interactions, the reduced product Fe2+ forms a weak Fe-O surface that is conducive to the adsorption of active substances. The presence of Fe-0 enhances the electrical conductivity of the catalytic, thus promoting ORR efficiency. Through redox coupling, the D -band center of Fe at FeCu@CN is optimized and brought close to the Fermi level to facilitate electron transfer. Notably, FeCu@CN demonstrates a superior power density of 2796.23 +/- 278.58 mW m(-3), far exceeding that of Pt/C (1363.93 +/- 102.56 mW m(-3)), in the application of microbial fuel cells (MFCs). Meanwhile, the MFC-loaded FeCu@CN maintains excellent stability and outstanding output voltage after 1000 h, which provides feasibility for large-scale application. (C) 2022 Elsevier Inc. All rights reserved.
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| 8. |
- Tang, Jinfeng, 1984, et al.
(författare)
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Assessment of copper and zinc recovery from MSWI fly ash in Guangzhou based on a hydrometallurgical process
- 2018
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Ingår i: Waste Management. - : Elsevier BV. - 0956-053X .- 1879-2456. ; 76, s. 225-233
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Tidskriftsartikel (refereegranskat)abstract
- Fly ash commonly accumulates a significant amount of heavy metals and most of these heavy metals are toxic and easily leached out to the environment, posing risks to human health. Thus, fly ash has been classified as a type of hazardous waste and requires proper treatment before disposal in specific landfill sites for hazardous waste. In this study, a hydrometallurgical process developed to recover copper and zinc performed in pilot scale close to industrial scale followed by a landfill compliance leaching test of the ash residue is evaluated. LIX860N-I and Cyanex 572 gave high selectively for extractions, a yield efficiency of 95% and 61% was achieved for copper and zinc respectively. Results of pilot experiments reveals that the combining metal recovery recycling and landfill disposal of the ash residue in a local regular landfill was demonstrated to be a technically and economically effective strategy. Specifically, the economic and environmental aspects of a scenario, in which the fly ash generated in Guangzhou is processed were systematically assessed. the assessment results show that a 7.15 million US$ of total expense reduction, a less energy cost of 19k GJ as well as 2100 tons less CO2 emissions could be achieved annually comparing to the current alternative, direct disposal of the fly ash as hazardous waste. The results reveal that the hydrometallurgical process has industrial application potential on both economic and environmental aspects and further optimization of the process can give more accurate assessment of the cost and environment effect. In addition, leaching tests and evaluation of solid residue according to the regulations specific to the country should be studied in future.
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| 9. |
- Tang, Jinfeng, 1984, et al.
(författare)
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Assessment of heavy metals mobility and correlative recovery and decontamination from MSWI fly ash: Mechanism and hydrometallurgical process evaluation
- 2021
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Ingår i: Science of the Total Environment. - : Elsevier BV. - 0048-9697 .- 1879-1026. ; 768
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Tidskriftsartikel (refereegranskat)abstract
- Fly ash from municipal solid waste incineration (MSWI) enriches many leachable toxic metals which readily migrate into the environment, posing serious risks to the ecosystem and human. In this study, the elements mobility, leaching availability as well as the potential maximum amounts of heavy metals in fly ash were thoroughly evaluated. To decontaminate the toxic elements from resulting fly ash leachates, The aqueous zinc (Zn) was recovered using Cyanex 572, cadmium (Cd) and copper (Cu) were effectively removed through adsorption process by a self-assembled hierarchical hydroxyapatite (HAP) nanostructure. The removal mechanism of Cd, Cu and Zn by leaching, extraction and adsorption was revealed with the results from XRD, ICP-MS and SEM. The results showed that fly ash has a high mobility under maximum availability leaching test (95% of fly ash was dissolved), a recovery rate of 91% for Zn can be obtained using Cyanex 572, and a high adsorption rate (> 95% for both Cu and Cd) was reached using HAP for the pristine fly ash leachate. The outcomes from isothermal and kinetic study revealed that Langmuir isotherm and pseudo-second order model can well describe the Cd and Cu adsorption behavior. Economic assessment suggested that the application of HAP for the removal of Cd and Cu is a technically sound and economically feasible approach. The findings of this study demonstrated that this comprehensive process integrated leaching, solvent extraction and consequential decontamination can be a practical strategy for MSWI fly ash treatment.
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| 10. |
- Tang, Jinfeng, 1984, et al.
(författare)
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Highly efficient recovery and clean-up of four heavy metals from MSWI fly ash by integrating leaching, selective extraction and adsorption
- 2019
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Ingår i: Journal of Cleaner Production. - : Elsevier BV. - 0959-6526. ; 234, s. 139-149
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Tidskriftsartikel (refereegranskat)abstract
- Municipal solid waste incineration (MSWI) fly ash contains significant amounts of heavy metals (e.g., Cd, Cu, Pb and Zn) and is therefore considered to be a hazardous waste requiring proper treatment prior to its disposal. In this work, an integrated hydrometallurgical process for treatment of MSWI fly ash was evaluated. Valuable metals, e.g. Cu and Zn, were first recovered by combining leaching and extraction sequentially. In the next step, the t removal of Cd and Pb from the remaining leachate using four types of iron-based adsorbents was evaluated. The leaching was optimized with respect to pH, leaching time and liquid to solid ratio. A test done under optimal conditions gave metal releases of 100% and 80% for Cu and Zn as well as 100% and 85% for Cd and Pb, respectively. The resulting leachate was contacted with organic phases based on kerosene containing the extractants LIX860N–I for Cu extraction and Cyanex 572 for Zn extraction in two consecutive steps. Efficient extractions were achieved, thus demonstrating that the combination of leaching and extraction can be successfully used for the recovery of Cu and Zn. Adsorption of heavy metal ions on various iron based sorbents to detoxify the aqueous effluent from the extraction showed good removal efficiency (more than 95%) for both Cd and Pb. The results of this study show that the proposed integrated process is a promising tool that can be used in the strategy for metal recovery and detoxification of MSWI fly ash.
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