RSC Advances
·
2018
·Vol. 8
·期 15
·8026-8038
·
IF 2.936
Shuli Liu,Zhengyang Duan,Changhua He,Xiaojun Xu,Tianguo Li,Yuhuan Li,Xuan Li,Yao Wang,Longqian Xu
Phosphate-modified baker's yeast (PMBY) was prepared, and used as a novel bio-sorbent for the adsorption of Pb2+ from aqueous solution. The influencing factors, absorption isotherms, kinetics, and mechanism were investigated. The scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR) characterization and elemental analysis of PMBY showed that phosphate groups were successfully grafted onto the surface of yeast. The kinetic studies suggested that the adsorption process followed a pseudo-second-order chemisorption. The adsorption process of Pb2+ using PMBY was spontaneous and endothermic. Furthermore, the adsorption of Pb2+ on PMBY can rapidly achieve adsorption equilibrium (in just 3 min), and the maximum adsorption capacity of Pb2+ on PMBY was found to be 92 mg g−1 at 30 °C, which was about 3 times that of the pristine baker's yeast. The suggested mechanism for Pb2+ adsorption on PMBY was based upon ion-exchange, electrostatic interaction and chelation between the phosphate groups and Pb2+. However, compared with the pristine baker's yeast, the higher capacity and rapid adsorption of PMBY for Pb2+ was mainly due to the chelation and electrostatic interactions between the phosphate groups and Pb2+. In addition, the regeneration experiments indicated that the PMBY was easily recovered through desorption in 0.01 M HCl, and that PMBY still exhibited 90.77% of the original adsorption capacity for Pb2+ after five regeneration cycles. These results showed the excellent regeneration capability of PMBY for Pb2+ adsorption. PMBY has shown significant potential for the removal of heavy metals from aqueous solution due to its rapid adsorption, high-capacity and facile preparation.
研究领域:
环境科学
·
生物化学
·
环境污染治理
·
重金属吸附
·
材料科学
✓ 已验证
DOI
高影响因子
ELECTROCHIMICA ACTA
·
2018
·
IF 5.116
Siwei Zhao,Ying Chen,Zhiyang Zhao,Longfei Jiang,Chi Zhang,Jianshou Kong,Xufei Zhu
Anodic TiO 2 nanotubes have been intensively studied for the application in supercapacitors , but the formation of nanograss is often avoided for the belief that it may retard capacitive performance. We fabricate TiO 2 nanotubes topped with nanograss by H 3 PO 4 solution soaking and hydrogenation doping, which in fact increases the capacitance of nanotubes in a fast and convenient way. The new structure exhibits an enhanced areal capacitance by up to 67.7% and by up to 23.5% after 2000 times of cycling. The capacitance generally increases with the nanotube length and reaches the maximum with an optimal nanograss length. The electric charge during hydrogenation doping is determined to quantify the general doping effect. Compared with ordinary nanotubes, nanograss has larger contact area with electrolyte during doping. Therefore, the grass-topped structure yields more electric charge and Ti 3+ during doping, which attributes to the improved capacitance.
研究领域:
材料科学
·
纳米技术
·
电化学
·
能源存储
·
表面工程
✓ 已验证
DOI
高影响因子
ELECTROCHIMICA ACTA
·
2019
·
IF 5.383
Bin Xiao,Wen-hai Zhang,Peng-bo Wang,Lin-bo Tang,Chang-sheng An,Zhen-jiang He,Hui Tong,Jun-chao Zheng,Bo Wang
Phosphate-based polyanion-structured materials have attracted considerable attention as anode materials in lithium-/sodium-ion batteries due to their stable crystal structure, affordability, and environmental friendliness. V 2 (PO 4 )O was encapsulated into crumpled nitrogen-doped graphene (VPO@N-G) through a facile spray-drying method in which VPO particles were completely encapsulated by N-doped graphene. For the first time, VPO@N-G was explored as an anode material for sodium-ion batteries. The Na + storage behavior of VPO@N-G was systematically investigated at the voltage range of 0.01–3.0 V (versus Na/Na + ). Results indicated that the VPO@N-G anode can deliver a highly reversible discharge capacity of 539 mAh g −1 at 0.05 A g −1 and achieve a highly reversible discharge capacity of 235.9 mAh g −1 even at a high current density of 10 A g −1 . Thus, VPO@N-G can be applied as a high-rate anode material for sodium-ion batteries.
研究领域:
材料科学
·
电化学
·
能源存储
·
纳米复合材料
·
无机功能材料
✓ 已验证
DOI
高影响因子
International Journal of Electrochemical Science
·
2023
·Vol. 11
·期 8
·7066-7075
·
IF 1.5
Jiheng Ding,Hongran Zhao,Lin Gu,Shengpei Su,Haibin Yu
This paper reports the synthesis of waterborne epoxy phosphate emulsion (WEP) through the reaction between epoxy resin E44 and phosphoric acid and ammonia neutralization. Synthesized WEP was characterized by FTIR for the confirmation of reaction between epoxy groups and phosphoric acid and SEM for morphology. WEP acted as a modifier in two-component epoxy anticorrosion coating on rusty steel substrate. The anticorrosion properties of the coating on rusty steel were investigated by electrochemical impedance spectroscopy (EIS) and Tafel polarization curve. Tafel polarization curve revealed that waterborne epoxy coating containing WEP had better protection ability which is clearly reflected by the protection efficiency (96.6%). EIS study also showed the higher impedance value for WEP containing coating as compared to pure waterborne epoxy coating.
研究领域:
材料科学
·
腐蚀与防护
·
高分子化学
·
表面工程
·
电化学
✓ 已验证
DOI
高影响因子
PROGRESS IN ORGANIC COATINGS
·
2019
·
IF 3.42
Youtong Wu,Shaoguo Wen,Kaiming Chen,Jihu Wang,Guangyu Wang,Kai Sun
Compared with solvent-based resins, waterborne resins still have defects such as insufficient anti-corrosion efficiency. In this paper, the sulfonated graphene/zinc phosphate composites were prepared as an anti-corrosion filler and doped into waterborne polyurethane resin. The morphology of composites is different from pure zinc phosphate. The optimal corrosion resistance can be obtained by adding 0.5 wt% sulfonated graphene/zinc phosphate fillers characterized by Potentiodynamic polarization curves and EIS analysis The corrosion current density ( i corr ) was 0.4252 μA/cm 2 and the charged transfer resistance (R ct ) was up to 10.937 × 10 3 Ω cm 2 , which show a good potential as anti-corrosive fillers in waterborne coatings system.
研究领域:
材料科学
·
高分子化学
·
表面工程
·
腐蚀与防护
·
涂层技术
✓ 已验证
DOI
高影响因子
Journal of Environmental Chemical Engineering
·
2024
·Vol. 12
·期 5
·114091
·
IF 7.4
Xiaolong Dai,Tiangui Qi,Xiaobin Li,Zhihong Peng,Guihua Liu,Qiusheng Zhou,Yilin Wang,Leiting Shen
In recent years, lithium iron phosphate (LFP) batteries have been widely used in the electric vehicle industry. The recycling of spent LFP will be propitious to conserving resources and alleviating the environmental risks it poses. In this study, a selective extraction method for lithium from spent LFP was proposed using nitric acid . Lithium leached into the liquid phase, while P and Fe remained in the leaching residue. Under the conditions of 120°C, HNO 3 /Li molar ratio of 2, and time of 2 h, the leaching efficiency of lithium reached 99.5 %, with a selectivity reaching 82.1 %. Initially, LFP was decomposed to liberate Li, Fe, and P in the liquid phase. Subsequently, ferrous ions were oxidized to trivalent, high-valent iron ions re-precipitated as FePO 4 ·2 H 2 O. Thermodynamic calculations indicate that the temperature and pH value of the extraction system have significant influence on both the oxidation and reprecipitation steps. An imbalance of Fe/P ratio (<1) in the raw material hinders the selectivity of lithium extraction , and supplementing this portion of Fe can enhance the selectivity to over 90 %. Additionally, LiCO 3 and anhydrous FePO 4 were effectively regenerated from the leachate and residue. This study provides a novel approach for the recycling of spent LFP and probably contributes to the sustainability of the lithium ion battery industry.
研究领域:
环境科学
·
冶金工程
·
材料回收
·
可持续能源
·
化学工程
✓ 已验证
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2017
·Vol. 43
·期 12
·9327-9333
·
IF 2.986
Nan Zhou,Shengxiong Huang,Tao Hong,Wei Luo,Yun Tian,Xiangyang Lu,Zhi Zhou
In this paper, LiTi 2 (PO 4 ) 3 @carbon composite as anode for aqueous lithium ion battery has been successfully synthesized by in-situ carbon coating method using oxalic acid and glucose as double carbon sources. XRD results confirm the rhombohedral NASICON-type LiTi 2 (PO 4 ) 3 structure of the as-prepared composite. The LiTi 2 (PO 4 ) 3 @carbon composite using double carbon sources (LTP-OG-10) disperses well, and the coated carbon layer has the appropriate thickness of 3–7 nm, which result in proper balance of the good electrical conductivity and the fast kinetics of diffusion of lithium ions . LTP-OG-10 exhibits better electrochemical performance compared with those using oxalic acid (LTP-O) or glucose (LTP-G) single carbon source. LTP-OG-10 anode delivers the discharge capacity of 112.5 mA h g −1 , 96.8 mA h g −1 , and 54.2 mA h g −1 at 0.2 C, 5 C and 20 C, respectively, much larger than that of LTP-O and LTP-G. Moreover, LTP-OG-10 demonstrated excellent cycling performance, with the capacity retention of 71.1% after 400 cycles at 0.2 C, 22.9% higher than that of LTP-G. The good electrochemical properties of LTP-OG-10 is mainly ascribed to the increase of defects, high-quality and appropriate thickness of carbon layer. Our study reveals that preparing LiTi 2 (PO 4 ) 3 @carbon composite using double carbon sources is an efficient approach to enhance its electrochemical properties.
研究领域:
材料科学
·
电化学
·
能源存储
·
无机非金属材料
·
功能材料
✓ 已验证
DOI
高影响因子
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
·
2011
·Vol. 13
·期 20
·9232-9237
·
IF 3.454
Jingjie Cui,Dehui Sun,Weijia Zhou,Hong Liu,Peiguang Hu,Na Ren,Haiming Qin,Zhen Huang,Jianjian Lin,Houyi Ma
Two kinds of TiO2 nanobelts were prepared from commercial P-25 powders via an alkaline hydrothermal method with and without an acid etching process. The uncauterized nanobelts (TNs) exhibited a smooth surface, and mixed phases of anatase and TiO2 (B), whereas the cauterized ones (CTNs) displayed a rough surface and a pure anatase structure. TNs and CTNs were then deposited onto a glassy carbon electrode (GCE) surface with a conductive adhesive (CA), and the resulting chemically modified electrodes exhibited electrocatalytic activities in the oxidation of nucleobases in a 0.1 M phosphate buffer solution (PBS) at pH 7.4. For guanine and adenine, well-defined oxidation peaks were observed in voltammetric measurements at about +0.62 and +0.89 V, respectively, at a potential sweep rate of 100 mV s−1, whereas for cytosine, uracil and thymine, the voltammetric features were not obvious. The average surface coverages (Γ) of guanine and adenine on the CTNs/CA/GCE electrode were estimated to be 4.75 × 10−10 and 7.44 × 10−10 mol cm−2, respectively, which were about twice those at the TNs/CA/GCE electrode. The enhanced activity of the CTN-based electrode towards purine nucleobase oxidation was ascribed to the large specific surface area and anatase structures with enhanced (001) facets of the CTN that facilitated adsorption of the analytes onto the electrode surface and charge transport through the electrode surface layer.
研究领域:
分析化学
·
纳米材料科学
·
电化学
·
生物传感
·
分子生物学
·
生物医学工程
✓ 已验证
DOI
高影响因子
Advanced Sustainable Systems
·
2024
·Vol. 8
·期 8
·2400098
·
IF 6.5
Fuyu Xiao,Wenbin Lai,Shihan Zeng,Lingjun He,Mingyang Ge,Fenqiang Luo,Peixun Xiong,Hui Lin,Chuyuan Lin,Yongjin Luo,Jixiang Zhang,Qingrong Qian,Qinghua Chen,Lingxing Zeng
The resource scarcity and pollution leakage risk caused by discarding the spent power lithium-ion batteries has aroused growing concern. Recovering and regenerating the cathode material from spent power lithium-ion batteries in an easy and environmentally friendly manner remains a significant challenge and an area of focus in battery research. Hence, a green and convenient method to recover FePO 4 from spent LiFePO 4 cathode powder by using Na 2 S 2 O 8 as an oxidizer and as cathode materials for lithium/sodium-ion batteries (LIBs/SIBs) is reported. Benefiting from the remarkable graphene oxide (GO) and vanadium oxide (V 2 O 5 ) coating, the regenerated FePO 4 –V 2 O 5 –graphene oxide (FePO 4 –V 2 O 5 –GO) is suitable for Li/Na storage (153 mAh g −1 at 0.2C/118 mAh g −1 at 0.5C). The high capacity retention, that stable for 300 cycles in LIBs and 300 cycles for SIBs, is also realized due to the stable structure. This work provides a green strategy for regenerating the cathode of spent lithium-ion batteries and designing cathodes of alkali metal ion batteries.
研究领域:
材料科学
·
电化学
·
能源存储
·
环境科学
·
资源回收
·
纳米材料
·
电池技术
✓ 已验证
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2020
·Vol. 31
·期 4
·2887-2894
·
IF 2.22
Liu Yuan,Gu Yi-Jing,Deng Jia-Li,Luo Gui-Yang,Wu Fu-Zhong,Mai Yi,Dai Xin-Yi,Li Jun-Qi
A series of LiFe 1− x Mn x PO 4 /C composites were successfully synthesized through a simple hydrothermal method. The effects of doped Mn on their micro-structures and electrochemical performances were investigated. The XRD results indicate that Mn doping cannot change the olivine lattice type of LiFePO 4 . Appropriate Mn doping can reduce the particle size of LiFePO 4 . The electrochemical performance data show that the electrochemical performances of the composite materials are enhanced at first and then decrease as the doping amount of Mn increases. Both the CV and EIS results illustrate that a small amount of doped Mn will reduce the electrode polarization and electrochemical impedance of the samples and simultaneously improve the electrochemical performance. Among all the samples, the LiFe 0.98 Mn 0.02 PO 4 /C sample has a desirable electrochemical performance, with its specific discharge capacity reaching 156.0 mAh g −1 at a rate of 0.1 C. Even at a high rate of 5 C, it can still reach 110.0 mAh g −1 . All the results indicate that an appropriate amount of doped Mn has an emphatic effect on the electrochemical performance of LiFePO 4 /C.
研究领域:
材料科学
·
电化学
·
能源存储
·
无机化学
·
纳米材料
·
固态化学
✓ 已验证
DOI
高影响因子
INORGANIC CHEMISTRY COMMUNICATIONS
·
2022
·
IF 3.428
Baoqin Mu,Bin Li,Bin Qi
Lanthanide metal–organic framework Ln-MOFs(Ln = Sm, Dy, Dy/Sm) were synthesized by hydrothermal method at 100 °C for 12 h using lanthanide metals (Ln = Sm, Dy, Dy/Sm) as metal ion centers and 1,3,5-benzotrioic acid (H 3 BTC) as ligands. The structural characteristics of Ln(BTC)(H 2 O)·(DMF) were characterized by X-ray Diffraction(XRD), Fourier Transform Infrared Spectroscopy(FT-IR) and Thermogravimetric Analysis(TGA). Scanning electron microscopy showed that the samples showed rod-like morphology, and the fluorescence spectra showed 478 nm and 573 nm corresponding to the characteristic transitions of 4 F 9/2 → 6 H 15/2 (blue light) and 4 F 9/2 → 6 H 13/2 (yellow light) of Dy 3+ , respectively, while orange light at 600 nm and red light at 646 nm corresponded to the characteristic transitions of 4 G 5/2 → 6 H 7/2 and 4 G 5/2 → 6 H 9/2 of Sm 3+ , demonstrating that the double-doped lanthanide metal ions MOF were successfully synthesized. H 7 (P(Mo 2 O 7 ) 6 )/(Dy/Sm-MOF) was used as a sensor for the determination of H 2 PO 4 − , the results of performance evaluation showed that the electrochemical sensor showed a linear relationship between 0.01 and 0.17 mM for H 2 PO 4 − , with a detection limit of 0.005 mM/L, good stability and reproducibility, which opened up a new way for the detection of orthophosphate dihydrogen.
研究领域:
分析化学
·
材料科学
·
电化学
·
无机化学
·
传感器技术
✓ 已验证
DOI
高影响因子
Advanced Energy Materials
·
2017
·Vol. 7
·期 15
·1700087
·
IF 16.721
Ting Jin,Yongchang Liu,Yang Li,Kangzhe Cao,Xiaojun Wang,Lifang Jiao
NaVPO 4 F has received a great deal of attention as cathode material for Na-ion batteries due to its high theoretical capacity (143 mA h g −1 ), high voltage platform, and structural stability. Novel NaVPO 4 F/C nanofibers are successfully prepared via a feasible electrospinning method and subsequent heat treatment as self-standing cathode for Na-ion batteries. Based on the morphological and microstructural characterization, it can be seen that the NaVPO 4 F/C nanofibers are smooth and continuous with NaVPO 4 F nanoparticles (≈6 nm) embedded in porous carbon matrix. For Na-storage, this electrode exhibits extraordinary electrochemical performance: a high capacity (126.3 mA h g −1 at 1 C), a superior rate capability (61.2 mA h g −1 at 50 C), and ultralong cyclability (96.5% capacity retention after 1000 cycles at 2 C). 1D NaVPO 4 F/C nanofibers that interlink into 3D conductive network improve the conductivity of NaVPO 4 F, and effectively restrain the aggregation of NaVPO 4 F particles during charge/discharge process, leading to the high performance.
研究领域:
材料科学
·
电化学
·
纳米技术
·
能源存储
·
无机非金属材料
·
固态化学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）