REACTIVE & FUNCTIONAL POLYMERS
·
2019
·
IF 3.074
Jiajie Zhu,Junbin Liao,Wei Jin,Bin Luo,Pengxin Shen,Arcadio Sotto,Jiangnan Shen,Congjie Gao
Exploring a desirable cross-linker applied in cation exchange membranes (CEMs) to improve dimensional stability as well as electrochemical performance has a great signifcance for the current membrane science and technology. In this investigation, a sequence of crosslinked sulphonated polysulfone (SPSF) CEMs has been prepared to explore the influence of the crosslinking functionality on the dimensional stability and electrodialysis (ED) performance of modified membranes. Different cross-linker structures were obtained according to the cross-linker agent content added during the synthesis route. As expected, the membrane surface became smoother with increasing cross-linker content, presumably as result of the denser structure established. The dimension stability increases according to the crosslinking degree applied, whereas the permselectivity of membranes depends on the conjunction of many important and interlinked factors, including the formation of narrow ion transport channels and the variations in the exchanges sites concentration. It was observed that the optimized CEM (60SPSF-C2#) showed the highest NaCl removal ratio (91.7%) during the desalination experiments and exhibited the higher current efficiency (95.7%) and lowest energy consumption (6.55 kWh kg −1 ). These results suggest the formation of the optimum three-dimensional network configuration for the membrane structure determined by the functionality of cross-liker selected in this investigation.
研究领域:
膜科学
·
电化学
·
材料科学
·
水处理
✓ 已验证
产品关联
DOI
高影响因子
ACS Omega
·
2019
·
IF 2.584
Jiajie Zhu,Bin Luo,Yukun Qian,Arcadio Sotto,Congjie Gao,Jiangnan Shen
In this study, a simple and facile approach was proposed to synthesize silver nanoparticles (AgNPs) loaded cation-exchange membranes (CEMs). A wide analytical study involving scanning electronic microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy was accomplished to corroborate that the in situ generated AgNPs were uniformly dispersed in the polymer matrix. In addition, as a result of the proposed synthesis strategy, the cross-linking structure inside the membrane was formed. The proper particle size and dispersibility of the AgNPs improved the mechanical properties of the membranes. Besides, the optimal AgNP-loaded CEM exhibited excellent bacterial killing activities against Gram-negative bacteria and showed a controlled improvement in the electrochemical performance of the prepared membranes. These effects were caused by the obtained distribution of AgNPs near ion-exchange groups that increased the aggregation of water molecules around them, improving the efficiency of ion transport due the formation of array broad ion-transport channels. The optimized CEM [sulfonated polysulfone (60SPSF)-C3#-Ag-2] exhibited an enhanced NaCl removal ratio of 67.5% with a high current efficiency (96.9%) and a low energy consumption (5.84 kWh kg–1). The distance of the inhibition zone from the boundary of the membrane of SPSF-C3#-Ag-2 reached 4.8 mm. These results led us to suggest that the proposed synthesis strategy may have potential applications in the field of antibacterial and desalting ion-exchange membranes.
研究领域:
材料科学
·
化学工程
·
环境科学
·
纳米技术
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF MEMBRANE SCIENCE
·
2018
·
IF 6.578
Junbin Liao,Jiajie Zhu,Shanshan Yang,Nengxiu Pan,Xinyan Yu,Chao Wang,Jun Li,Jiangnan Shen
Developing highly ion conductive and desirable electrodialysis (ED) performance anion exchange membranes (AEMs) is of great significance. In this work, we report a strategy for fabricating novel AEMs based on a series of fluoro-methyl poly(arylene ether ketone)s having long-side-chain imidazolium groups for ED. Having hydrophilic conductive flexible side-chain imidazolium groups and rigid hydrophobic backbone within AEM matrix, the optimized AEM (PAEK-60-im) shows low water uptake of 24.9% at 80 °C and desirable ion conductivity of 22.01 mS cm –1 at 30 °C. In NaCl removal application of ED, PAEK-60-im shows the NaCl removal ratio of 69.66% within 120 min, outperforming commercial AEM-Type II (68.98%). Accordingly, it has a higher current efficiency of 83.7% but lower energy consumption of 5.9 kWh kg –1 , compared with the commercial one (82.0%; 6.6 kWh kg –1 ). In particular, in selectrodialysis application, possibly owing to the synergistic effect of pore-size sieving effect resulting from macro-separation morphology and hydration energy difference of SO 4 2– ions (–1000 kJ mol –1 ) and Cl – ions (–317 kJ mol –1 ) in feeding solution, PAEK-60-im shows significantly superior monovalent anion perm-selectivity (Cl − /SO 4 2− ) of 7.70 at 30 min, relative to commercial anion-selective Neosepta ACS (5.27) and many other reported mono-valent anion selective AEMs having elegant surface modified layers. The superior ED performance of the homogeneous PAEK-60-im is suggestive of its potential separation application.
研究领域:
材料科学
·
化学工程
·
电化学
·
膜技术
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2019
·
IF 8.355
Jie Ma,Lei Wang,Fei Yu,Xiaohu Dai
Due to its low energy consumption, capacitive deionization (CDI) is regarded as one of the most promising technologies in brackish water desalination. However, CDI has two drawbacks, namely, low deionization capacity and unavoidable parasitic reactions that limit its further development. Unlike the traditional CDI electrodes that store the ions in the electric double layer capacitors, faradic electrodes store ions at crystallographic sites or between the atomic planes, which could effectively address the issues mentioned above. However, obtaining low-cost faradic electrode materials with a high salt removal capacity for practical applications is still challenging. Here, we report a new material, mesoporous amorphous FePO 4 nanosphere@Graphene (FePO 4 @RGO) synthesized via a one-step hydrothermal method. Electrochemical experiments demonstrate that the formation of a mesoporous structure and covered by graphene can address the drawbacks of pure FePO 4 for electroconductivity and ion diffusion rates. When used in desalination, the novel design enhances the desalination capacity, and the rates increase by 60% (50.13–85.94 mg/g) and 180% (0.079–0.24 mg/g/s), respectively, while energy consumption decreases by 25%. The production cost of the material was calculated, and implies that this material has potential for use in large-scale desalination.
研究领域:
环境科学
·
材料科学
·
水处理
✓ 已验证
DOI
高影响因子
WATER RESEARCH
·
2023
·
IF 12.8
Xing Wang,Mengjun liang,Jiancong Zhang,Xuncai Chen,Mono Zaw,Than Zaw Oo,Nyein Wint Lwin,Su Htike Aung,Yuan Chen,Fuming Chen
High energy consumption and low salt removal rate are key barriers to realizing practical electrochemical seawater desalination processes. Here, we demonstrate a novel solar-driven redox flow desalination device with double photoelectrodes to achieve efficient desalination without electrical energy consumption. The device consists of three parts: one photoanode unit, one photocathode unit, and one redox flow desalination unit sandwiched between the two photoelectrode units. The photoelectrode units include a TiO 2 photoanode and a NiO photocathode sensitized with N719 dye, triiodide/iodide redox electrolyte, and graphite paper integrated electrodes decorated with 3,4-ethylene-dioxythiophene. Two salt feeds are located between two ferro/ferricyanide redox flow chambers. Under light illumination, high-quality freshwater is obtained from brackish water containing different concentrations of NaCl from 1000 to 12,000 ppm with a high NaCl removal rate. The device can work in multiple desalination cycles without significant performance declines. Furthermore, natural seawater with an ionic conductivity of 53.45 mS cm −1 is desalinated to freshwater. This new design opens opportunities to realize efficient and practical solar-driven desalination processes.
研究领域:
环境科学
·
材料科学
·
化学工程
·
太阳能
✓ 已验证
产品关联
DOI
PubMed
高影响因子