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JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY · 2022 · IF 6.76

Construction of polysulfone anion exchange hybrid membranes by incorporating carbon quantum dots and facilitated transport mechanisms

Yuan Jin,Xiu Zhang,Tianci Feng,Meisheng Li,Huifang Xiao,Shouyong Zhou,Yijiang Zhao,Jing Zhong,Dawei Yang

Low ion conductivity and poor alkali resistance are still the two major obstacles for the applications of anion exchange membranes (AEMs). In this work, the combined strategies of Carbon quantum dots (CQDs) hybrid and cross-linking modification via side-chains designing were employed to prepare organic–inorganic hybrid AEMs. Then, the cross-linked quaternized polysulfone (CQPSf-CQDs) hybrid AEMs by incorporating carbon quantum dots were successfully fabricated. After hybrid and cross-linking, the mechanical properties of CQPSf-CQDs hybrid AEMs were higher than that of the pristine one, reaching 49.4 MPa for the best one. Meanwhile, the existence of CQDs can expand the hydrophilic area in the membrane, which is beneficial to the transport of O H - . The incorporated CQDs interact weakly with cationic groups in the side chains through hydrogen bonds. The simulation results further demonstrated that the introduction of CQDs was beneficial to the construction of hydrophilic and hydrophobic domains, thereby increasing O H - conductivity. In addition, the prepared hybrid membranes own excellent dimensional stabilities and ion transport performances. These preliminary results give us a lot of hopes for further experiments and optimizations for the hybrid AEMs.

研究领域: 材料科学 · 高分子化学 · 膜科学与技术 · 电化学 · 能源材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS · 2018 · IF 2.831

Hypercrosslinked strong anion-exchange polymers for selective extraction of fluoroquinolones in milk samples

Xiaoping Liang,Ping Hu,Hongyang Zhang,Wen Tan

In this work, hypercrosslinked strong anion-exchange polymer resins (HXLPP-SAX) were synthesized and evaluated as solid-phase extraction (SPE) sorbents for extracting fluoroquinolones (FQs) in milk samples. These particles were prepared using a protocol that was facile and cost-effective by combining hypercrosslinking reactions and quaternisation reactions in one step. After the synthesis, the morphological properties and anion-exchange, adsorption, and selectivity performances of the HXLPP-SAX resins were characterized and evaluated. It was shown that the polymers were monodisperse microspheres, with the mean diameters of 2–4 μm, ion-exchange capacity (IEC) of 0.311 meq/g, and specific surface area more than 1000 m 2 /g. The resins applied as SPE sorbents possessed high selectivity in the extraction of amphoteric compounds (enoxacin and enrofloxacin as the representatives) followed by HPLC-UV analysis, as compared to commercially available strong anion-exchange sorbents (Oasis MAX). The SPE-HPLC-UV method was fully validated and exhibited good linearity (10–2000 ng/g, R 2 ≥ 0.997), low limits of detection (2.8–5.1 ng/g), good recoveries (85.8%–117.9%, RSDs ≤ 7.1%) and precisions (intra-day RSDs ≤ 7.7% and inter-day RSDs ≤ 9.4%). Then the method was performed the selective enrichment of six FQs (enoxacin, norfloxacin, ciprofloxacin, lomefloxacin, enrofloxacin, and sparfloxacin) in milk samples. The present results demonstrated that the proposed resins exhibited a promising potential for the enrichment and determination of FQ residues in milk samples as well as in other samples with complex matrices.

CAS / MDL: 1321-74-0
研究领域: 分析化学 · 食品科学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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DALTON TRANSACTIONS · 2012 ·Vol. 41 ·期 28 ·8567-8574 · IF 3.838

Luminescent hybrid materials of lanthanide β-diketonate and mesoporous host through covalent and ionic bonding with anion metathesis

Qiu-Ping Li,Bing Yan

Luminescent mesoporous materials were prepared by performing an anion metathesis reaction on ionic liquid modified SBA15, which has imidazolium chloride bridging units. The lanthanide β-diketonate complex anion was successfully anchored onto the SBA15 framework after the anion metathesis reaction. The resulting materials were characterized by FTIR, TEM, TGA, small-angle X-ray powder diffraction (SAXRD) and nitrogen adsorption–desorption isotherms. The photoluminescent properties of these materials were investigated in detail, and the results reveal that these hybrid mesoporous SBA15, prepared through this preparation approach, present favorable photoluminescent behavior such as high luminescent quantum efficiencies and long luminescent lifetimes.

研究领域: 材料化学 · 无机化学 · 光功能材料 · 纳米材料科学
✓ 已验证 DOI 高影响因子
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Advanced Science · 2019 ·Vol. 6 ·期 17 ·1900381 · IF 15.804

[Ln6O8] Cluster-Encapsulating Polyplumbites as New Polyoxometalate Members and Record Inorganic Anion-Exchange Materials for ReO4− Sequestration

Jian Lin,Lin Zhu,Zenghui Yue,Chuang Yang,Wei Liu,Thomas E. Albrecht-Schmitt,Jian-Qiang Wang,Shuao Wang

Various types of polyoxometalates (POMs) have been synthesized since the 19th century, but their assortment has been mostly limited to Groups 5 and 6 metals. Herein, a new family of POMs composed of a carbon group element as the addenda atoms with two distinct phases, LnPbOClO 4 -1 (Ln = Sm to Ho, Y) and LnPbOClO 4 -2 (Ln = Er and Tm) is reported. Both structures are built from [Ln 6 O 8 ] rare-earth metal hexamers being incorporated in [Pb 18 O 32 ]/[Pb 12 O 24 ] polyplumbites, and unbound perchlorates as charge-balancing anions. Impressively, YPbOClO 4 -1 and ErPbOClO 4 -2 exhibit exceptional uptake capacities (434.7 and 427.7 mg g −1 ) toward ReO 4 − , a chemical surrogate for the key radioactive fission product in the nuclear fuel cycle 99 TcO 4 − , which are the highest values among all inorganic anion-exchange materials reported until now. The sorption mechanism is clearly elucidated and visualized by single-crystal-to-single-crystal structural transformation from ErPbOClO 4 -2 to a perrhenate-containing complex ErPbOReO 4 , revealing a unique ReO 4 − uptake selectivity driven by specific interaction within Pb···O-ReO 3 − bonds.

研究领域: 无机化学 · 放射化学 · 环境化学 · 材料科学 · 核燃料循环
✓ 已验证 DOI 高影响因子
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CHINESE JOURNAL OF CHEMISTRY · 2011 ·Vol. 29 ·期 4 ·778-782 · IF 0.773

Determination of Glycolate Acid, Mono- and Dichloroacetic Acids in Synthetical Betaine by Anion-exchange Chromatography

Haining Shi,Zonghua Wang,Hui Wang,Rui Zhao,Mingyu Ding

An anion-exchange chromatography method combined solid phase extraction (SPE) was developed for the simultaneous analysis of glycolate acid (GL), monochloroacetic acid (MCA) and dichloroacetic acid (DCA) in synthetical betaine products. The analytes and unknown anionic impurities were well separated on a Metrosep A supp5 anion-exchange column (150 mm×4 mm) with 2.0 mmol/L Na 2 CO 3 +2.0 mmol/L NaHCO 3 solution as eluent. Suppressed conductivity detection was used. A strong cation exchange (SCX) solid phase extraction (SPE) cartridge was used to reduce the concentration of matrix betaine and a Cleanert IC-Ag pretreatment cartridge was used to remove high Cl − concentration. The detection limits of GL, MCA and DCA were 0.09, 0.017 and 0.05 µg/L, respectively. The relative standard deviations (RSDs) of the retention times and peak areas were less than 0.09% and 0.49%, respectively. The recoveries of the three analytes were between 90.6% and 100.8%. The analytical results showed that GL and DCA were present in high concentration and no MCA was found when the proposed ion chromatography method was applied to three synthetical betaine samples. The proposed method is simple, sensitive and timesaving, and is also suitable for routine analysis in quality control of synthetical betaine products.

研究领域: 分析化学 · 药物质量控制 · 分离科学 · 环境分析 · 食品化学
✓ 已验证 DOI 高影响因子
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Journal of the Taiwan Institute of Chemical Engineers · 2019 · IF 3.834

Surface-modified anion exchange membranes with self-cleaning ability and enhanced antifouling properties

Xiao Wang,George Q. Chen,Wei Zhang,Huining Deng

The development of reliable anion exchange membranes (AEMs) with superior antifouling properties is critical in practical applications of electrodialysis processes. For the first time, the AEMs were modified by poly (sodium 4-styrene sulfonate) (PSS) with titanium dioxide (TiO 2 ) nanoparticles using only one electrodeposition step to stabilize the nanoparticles on the membrane surface while improving their antifouling ability. Owing to the bonding between the sulfonic groups of PSS and TiO 2 , the TiO 2 nanoparticles were well dispersed in the modified layer. The deposition of PSS endowed the AEMs with a negatively charged surface, while the addition of TiO 2 nanoparticles further increased the charge density. The membrane resistance increased only marginally after 100-min of fouling experiments using sodium dodecyl benzene sulfonate (SDBS), due to the presence of TiO 2 on the modified AEMs. Ultraviolet (UV) irradiation was proven to be an effective approach in inducing good fouling reversibility of the TiO 2 -PSS modified AEMs through photocatalytic decomposition and hydrophilicity improvement.

研究领域: 膜科学 · 环境工程 · 材料化学 · 电化学 · 水处理技术
✓ 已验证 DOI 高影响因子
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Desalination and Water Treatment · 2024 · IF 1

Surface coating of a side-chain type polyelectrolyte for endowing perm-selectivity between specific anions to an anion-exchange membrane with a small loss of membrane conductivity

Yan-zhen Shen,Xun-liang Wang,Yu-xiang Jia,Meng Wang

The endowment of perm-selectivity for specific ions will further extend the applications of heterogeneous membrane. In this work, a side-chain type weak cationic polyelectrolyte, PVDF-g-PVP, was synthesized for surface hydrophobilization of heterogeneous anion-exchange membrane (AEM) in order to impart perm-selectivity between specific anions with different Gibbs hydration energy. After microstructure observation and chemical composition analyses by SEM, AFM, EA and FTIR, the perm-selectivity between specific anions, electrical resistance, transport number, limiting current density, surface homogeneity, as well as salt permeability of the modified AEMs were investigated. Series of electrodialysis experiments in SO 4 2– /Cl – system indicated that a significant perm-selectivity was indeed achieved by the attachment of PVDF-g-PVP coating. In particular, it was worth noting that only a small loss of membrane conductivity was observed after the functionalization. This should be closely related to the micro-phase separation morphology of the coating layer which was induced by the polarity difference between the main chains and side chains of PVDF-g-PVP. Besides, the chronopotentiometric analyses indicated surface homogeneity of the heterogeneous AEM was significantly enhanced and then effectively ameliorated concentration polarization behaviors at the membrane-solution interface. Meanwhile, the perm-selectivity for co-ions was also improved and suppressed back diffusion behaviors of salt driven by concentration gradient. In brief, the modifying scheme proposed in this work can effectively improve comprehensive transport properties of conventional heterogeneous AEM.

研究领域: 膜科学与技术 · 高分子材料化学 · 分离科学 · 电化学工程 · 功能材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF MEMBRANE SCIENCE · 2018 · IF 6.578

Imidazolium-functionalized poly (arylene ether ketone) cross-linked anion exchange membranes

Xinming Du,Zhe Wang,Wenchang Liu,Jingmei Xu,Zhaoyu Chen,Chunmei Wang

A series of phenolphthalein-based poly (arylene ether ketone) (PEK) copolymer are synthesized to prepare anion exchange membranes (AEMs). The ion group 1-vinyl imidazole is introduced on the unit of phenolphthalein-based as a hydrophilic segment and cross-linking agent. The structure of resulting membranes was investigated by 1 H NMR and FT-IR. The well-defined microphase-separated structures were verified by TEM and SAXS profiles. The cross-linked membrane of ImPEK-0.4 exhibits high hydroxide conductivity (0.0836 S/cm, at 80 °C), excellent mechanical performance (69.6 MPa) and the maximum swelling ratio is only 7.95% at 80 °C. Furthermore, the excellent alkaline stability is demonstrated by immersing the prepared membrane in 1 M NaOH at 40 °C for 400 h. The ionic conductivity is still high to 0.0381 S/cm for ImPEK-0.4. These results indicate that combining phase separation architecture and crosslinking may possess potential applications for alkaline fuel cells (AFCs).

研究领域: 高分子材料科学 · 电化学能源材料 · 燃料电池技术 · 膜分离工程 · 聚合物化学
✓ 已验证 DOI 高影响因子
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CHEMOSPHERE · 2021 · IF 7.086

Enhanced fluoride removal from water by nanosized cerium oxides impregnated porous polystyrene anion exchanger

Hao Dong,Huan Tang,Xinxing Shi,Wenlan Yang,Wenjing Chen,Han Li,Yu Zhao,Zhengyong Zhang,Ming Hua

Efficient elimination of fluoride from wastewater is an urgent need for ensuring water safety. In the present study, a stable and reusable nanocomposite (NCO@PAE) was synthesized by impregnating nanosized cerium oxides (NCO) inside a porous polystyrene anion exchanger (PAE) host for efficient fluoride removal from wastewater. The newly fabricated NCO@PAE exhibited excellent resistance to acid and alkali environment, allowing it to be utilized in a wide pH range (2–12). Fluoride uptake onto NCO@PAE was a pH-dependent process, which could reach the maximum capacity at pH 3.0. Compared with its host PAE , NCO@PAE showed conspicuous adsorption affinity towards fluoride in the coexistence of other competing anions at high concentrations. Adsorption kinetics confirmed its high efficiency for achieving equilibrium within 120 min. Fixed-bed adsorption runs demonstrated that the effective processing capacity of NCO@PAE for synthetic fluoride-containing wastewater (initial fluoride 2.5 mg/L) was about ~330 BV (bed volume), while only 22 BV for the host PAE . The exhausted NCO@PAE could be effectively revived by a simple in-situ desorption method for long-term cycle operation without conspicuous capacity loss. All the results indicated that NCO@PAE is a reliable and promising adsorbent for water defluoridation.

研究领域: 环境科学 · 水处理技术 · 材料科学 · 吸附化学 · 环境功能材料
✓ 已验证 DOI 高影响因子
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RSC Advances · 2014 ·Vol. 4 ·期 78 ·41398-41410 · IF 3.708

Cross-linked multiblock copoly(arylene ether sulfone) ionomer/nano-ZrO2 composite anion exchange membranes for alkaline fuel cells

Xiuhua Li,Jinxiong Tao,Guanghui Nie,Liuchan Wang,Liuhong Li,Shijun Liao

A series of cross-linked multiblock copoly(arylene ether sulfone) ionomer/nano-ZrO2 (CLQCPAES/nano-ZrO2) composite anion exchange membranes were prepared via block copolymerization, bromomethylation, ultrasonication blending, self-crosslinking, quaternization and alkalization. The structure, and the surface and cross section morphology of the CLQCPAES/nano-ZrO2 composite membranes were characterized by solubility tests, FT-IR, XRD and SEM analyses. The combination of the determined results revealed that the CLQCPAES/nano-ZrO2 composite membranes are a complex cross-linking networks of hydrophobic domains/hydrophilic domains/nano-ZrO2 with a clear zonal distribution of uniform nano-sized particles in the hydrophilic domains, when the nano-filler loading was below 7.5%. Basic performances of the CLQCPAES/nano-ZrO2 composite membranes were assessed to investigate their application in fuel cells in terms of the water uptake, swelling ratio, ion exchange capacity (IEC), hydroxide conductivity, thermal and mechanical properties, and alkaline stability. The modification of anion exchange membranes with multiblock ionomer structures, the use of a cross-linking technique and the introduction of nano-ZrO2 particles greatly enhanced the water uptake, hydroxide conductivity, mechanical properties and alkaline stability of the composite membranes. In particular, the CLQCPAES/7.5%ZrO2 membrane with an IEC value of 1.23 mmol g−1 exhibited the best comprehensive properties and constitutes a good potential candidate for an anion exchange membrane to be used in AEMFCs.

研究领域: 高分子材料科学 · 电化学 · 能源材料 · 膜科学与技术 · 燃料电池 · 纳米复合材料 · 功能高分子
✓ 已验证 DOI 高影响因子
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JOURNAL OF POWER SOURCES · 2022 · IF 9.794

Interfacial water distribution behaviors in high performance bipolar membrane fuel cell

Zhengjian Li,Sian Chen,Liting Cui,Haining Wang,Shanfu Lu,Yan Xiang

The acidic-alkaline interface of a bipolar membrane fuel cell (BPMFC) is the place to generate water, which significantly affect the output performance of BPMFC by regulating the water distribution due to the ion conductivity and oxygen reduction reaction (ORR) kinetics in cathode. To investigate the influence of water diffusivity ( D w ) on the water distribution, four alkaline polymer electrolytes with different D w is selected as anion exchange membrane or alkaline electrolyte ionomer to assemble BPMFCs. A combined experimental and simulated study reveals the positive correlation relationship of D w to the water distribution and performance of BPMFC. By increasing the D w of the alkaline polymer electrolytes, the interfacial-generated water amount can be increased and promptly transport to the cathode, thereby satisfying the ion conductivity and increasing the ORR kinetics, and breakthrough the peak power density of the BPMFC with 1.06 W cm −2 without humidification .

研究领域: 电化学 · 能源材料 · 燃料电池 · 高分子科学 · 界面科学
✓ 已验证 DOI 高影响因子
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REACTIVE & FUNCTIONAL POLYMERS · 2019 · IF 3.074

Templated synthesis of cyclic poly(ionic liquid)s

Qingquan Tang,Weiyi Zhang,Jiayin Yuan,Qiang Zhao

Charged cyclic polymers, e.g. cyclic DNAs and polypeptides , play enabling roles in organisms, but their synthesis was challenging due to the well-known “polyelectrolyte effect”. To tackle the challenge, we developed a templated method to synthesize a library of imidazolium and pyridinium based cyclic poly(ionic liquid)s. Cyclic templates, cyclic polyimidazole and poly(2-pyridine), were synthesized first through ring-closure method by light-induced Diels−Alder click reaction. Through quaternization of cyclic templates followed by anion metathesis, the cyclic poly(ionic liquid)s were synthesized, which paired with varied counter anions.

研究领域: 高分子化学 · 有机合成 · 功能材料 · 离子液体 · 生物医用材料
✓ 已验证 DOI 高影响因子
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