以氯甲基杂环聚醚酮(CMPPEK)为原料,加入三乙胺进行铵化,并分别加入二乙烯三胺(DETA)和二乙胺(DEA),生成的仲胺基(或叔胺基)与邻近分子链氯甲基团进行自交联.经过制膜和离子交换反应,制备了DETA自交联杂萘联苯聚芳醚阴离子交换膜(DETA-Q...以氯甲基杂环聚醚酮(CMPPEK)为原料,加入三乙胺进行铵化,并分别加入二乙烯三胺(DETA)和二乙胺(DEA),生成的仲胺基(或叔胺基)与邻近分子链氯甲基团进行自交联.经过制膜和离子交换反应,制备了DETA自交联杂萘联苯聚芳醚阴离子交换膜(DETA-QPPEK-OH)和DEA自交联杂萘联苯聚芳醚阴离子交换膜(DEA-QPPEK-OH).采用傅里叶变换红外(FTIR)光谱对制备自交联膜的化学结构进行表征.研究了DETA-QPPEK-OH和DEA-QPPEK-OH膜的理化性质,结果表明前者具有较低吸水率和更低溶胀度.通过研究DETAQPPEK-OH和DEA-QPPEK-OH膜的离子传导率随温度的变化规律,结果表明在80°C时其离子传导率分别达到0.060和0.028 S cm-1,表明本文制备的自交联膜具有较高离子传导率.此外还通过热重分析(TGA)对两类自交联膜的热稳定性进行了研究.展开更多
以CO_3^(2-)为检测对象,发展了聚合物敏感膜电位型碳酸根传感器。采用3-辛基噻吩(POT)作为传导层的固体接触式电极技术,通过优化实验条件,构建了聚合物敏感膜CO_3^(2-)选择性电极,该电极对CO_3^(2-)检出限为7.0μmol/L,线性范围为1.0...以CO_3^(2-)为检测对象,发展了聚合物敏感膜电位型碳酸根传感器。采用3-辛基噻吩(POT)作为传导层的固体接触式电极技术,通过优化实验条件,构建了聚合物敏感膜CO_3^(2-)选择性电极,该电极对CO_3^(2-)检出限为7.0μmol/L,线性范围为1.0×10^(-5)~1.0×10^(-3)mol/L,能斯特响应斜率为-29.6 m V/decade。传感器已用于海水中CO_3^(2-)的测定。展开更多
The Cu(Ⅱ) separation behaviors with polymer inclusion membranes(PIMs) are explored by modifying 2-aminomethylpyridine derivatives with hydrophobic alkyl chains, including 2-[N-(tert-butyloxycarbonylmethyl)-2-picolyam...The Cu(Ⅱ) separation behaviors with polymer inclusion membranes(PIMs) are explored by modifying 2-aminomethylpyridine derivatives with hydrophobic alkyl chains, including 2-[N-(tert-butyloxycarbonylmethyl)-2-picolyamino]acetate(AMB), N,N-dioctyl-2-aminomethylpyridine(AMD), tert-butyl 2-(N-octyl-2-picolyamino) acetate(AMC), and N,N-didecyl-2-aminomethylpyridine(AME). The transport flux and selectivity of Cu(Ⅱ) are determined by optimizing composition and structure of carriers and plasticizers. The results show that the hydrophobic modification of 2-aminomethylpyridine derivatives can boost the selective transport of copper ions in PIMs and membrane stability. In the optimum composition of 30 wt.% PVC, 30 wt.% AME, and 40 wt.% NPOE, the initial flux of Cu(Ⅱ) is 5.8×10^(−6) mol·m^(−2)·s^(−1). The FT-IR and XPS spectra identify that the alkyl amine functional groups of AME involve in the transport of copper chloride species. The SAXS analysis demonstrates that the generated micro-channels in PIMs induced by the hydrophobic modification of 2-aminomethylpyridine derivatives can contribute to the enhanced Cu(Ⅱ) flux.展开更多
Owing to the potential ability of metal nanoparticles to enhance the performance of energy storage devices,their catalytic performance has been studied by many researchers.However,a limited number of suitable characte...Owing to the potential ability of metal nanoparticles to enhance the performance of energy storage devices,their catalytic performance has been studied by many researchers.However,a limited number of suitable characterization techniques does not allow fully elucidating their catalytic mechanism.Herein,high‐accuracy operando magnetometry is employed to investigate the catalytic properties of a cobalt oxide electrode for lithium‐ion batteries fabricated by magnetron sputtering.Using this technique,the magnetic responses generated by the Co‐catalyzed reversible formation and decomposition of a polymer/gel‐like film are successfully detected.A series of CoO/Co films are prepared by magnetron sputtering in different environments at various sputtering times to study the influence of Co content and film thickness on their catalytic properties.It is clearly demonstrated that increasing the Co content enhances the magnetic signal associated with the catalysis process.Furthermore,decreasing the electrode thickness increases the area affected by the catalytic reactions,which in turn enhances the corresponding magnetic responses.The obtained results experimentally confirm the catalytic activity of Co metal nanoparticles and provide a scientific guidance for designing advanced energy storage devices.This work also shows that operando magnetometry is a versatile technique for studying the catalytic effects of transition metals.展开更多
In order to further improve the driving performance of ionic polymer metal composites(IPMCs),Nafion/graphene quantum dots(GQDs)hybrid membranes incorporating GQDs with various contents of 0,0.1 wt.%,0.5 wt.%,1.0 wt.%,...In order to further improve the driving performance of ionic polymer metal composites(IPMCs),Nafion/graphene quantum dots(GQDs)hybrid membranes incorporating GQDs with various contents of 0,0.1 wt.%,0.5 wt.%,1.0 wt.%,2.0 wt.%and 4.0 wt.%were fabricated by solution casting,and then IPMCs were manufactured by electroless plating.The water contents and elastic moduli of the hybrid membranes were tested.The morphology characteristics of the hybrid membranes and the IPMCs were observed,and the current,AC impedance,blocking force and displacement of the IPMCs were measured.The results show that the elastic modulus of the hybrid membranes decreases,the water content increases,and the actuation performance of the IPMCs improves significantly after the addition of GQDs.IPMC with 1.0 wt.%GQDs exhibits the best driving property.Compared with the IPMC without GQDs,the working current,ion conductivity,blocking force,and tip displacement increase by 94.67%,311.11%,53.66%,and 66.07%,respectively.These results lay a solid foundation for the preparation of IPMCs with high performance,and further broaden their applications in biomedical devices and bionic robots.展开更多
In this paper, the effect of hydrogen reduction of silver ions on the performance and structure of new solid polymer electrolyte polyetherimide （PEI）/Pebax2533 （Polynylonl2/tetramethylene oxide block copolymer, PA1...In this paper, the effect of hydrogen reduction of silver ions on the performance and structure of new solid polymer electrolyte polyetherimide （PEI）/Pebax2533 （Polynylonl2/tetramethylene oxide block copolymer, PA12-PTMO）/AgBF4 composite membranes is investigated. For PEI/Pebax2533/AgBF4 composite membranesprepared with dillerent AgBF4 concentration, the permeances of propylene and ethylene increase with the increase of AgBF4 concentration due to the carrier-facilitated transport, resulting in a high selectivity. But for propyl- ene/propane mixture, the mixed-gas selectivity is lower than its ideal selectivity. The hydrogen reduction strongly influences the membrane performance, which causes the decrease of propylene permeance and the increase of pro-pane permeance. With the increase of hydrogen reduction time, the membranes show a clearly color change from white to brown, yielding a great selectivity loss. The data of X-ray diffraction and FT-IR prove that silver ions are reduced to Ago after hydrogen reduction, and aggregated on the surface of PEI/Pebax2533/AgBF4 composite mem- branes.展开更多
Organic soft actuators are of special interest in many fields including intravascular neurosurgery. Ion conductive polymer film （ICPF） actuators have been one of the strong candidates. The ICPF investigated here was...Organic soft actuators are of special interest in many fields including intravascular neurosurgery. Ion conductive polymer film （ICPF） actuators have been one of the strong candidates. The ICPF investigated here was a cation-exchange membrane （Nation 117, Du Pont）. When a voltage is given between the metal eIectrodes of an ICPF actuator, the ICPF actuator bends in the water due to the motion of Li＋ cations with associated water. In order to increase the freedom of the deformation of the ICPF actuator, structures of independent electrode pairs were proposed. The electrodes were selectively deposited by non-electrokvzed plating including the Pt [（NH3）6]^4＋ deposition process in a [Pt（NH3）6]Cl4 solution and the reduction process in a NaBH4 solution. Here, an elastomer adhesive tape with a fine electrode patterns was used performances were reported in detail. as a mask. The actuators processing conditions and their actuator展开更多
In order to effectively improve the properties of anion exchange membrane(AEM)materials,a series of novel poly(aryl ether nitrile)s with flexible side-chain-type quaternary phosphonium cations(PAEN-TPP-x)were designed...In order to effectively improve the properties of anion exchange membrane(AEM)materials,a series of novel poly(aryl ether nitrile)s with flexible side-chain-type quaternary phosphonium cations(PAEN-TPP-x)were designed and prepared on the basis of considering the influences of polymer backbone,cationic group species and the connection way between the cations and polymer chains.The synthetic method,structure and ion-exchange capacity,water absorption,swelling,hydroxide conductivity and alkaline stability of the obtained AEMs were studied.A comparative study with other reported AEMs was also performed for further exploration of the relationship between the structure and properties.These AEMs with flexible side-chain-type quaternary phosphonium cations displayed good comprehensive properties.Their water uptakes and swelling ratios were in the range of 11.6%–22.7%and 4.4%–7.8%at 60℃,respectively.They had hydroxide conductivity in the range of 28.6–45.8 mS cm^-1 at 60℃.Moreover,these AEMs also exhibited improved alkaline stability,and the hydroxide conductivity for PAEN-TPP-0.35 could remain 82.1%and 80.6%of its initial value at 60 and 90℃in 2 mol L^-1 NaOH solution for480 h,respectively.展开更多
文摘以氯甲基杂环聚醚酮(CMPPEK)为原料,加入三乙胺进行铵化,并分别加入二乙烯三胺(DETA)和二乙胺(DEA),生成的仲胺基(或叔胺基)与邻近分子链氯甲基团进行自交联.经过制膜和离子交换反应,制备了DETA自交联杂萘联苯聚芳醚阴离子交换膜(DETA-QPPEK-OH)和DEA自交联杂萘联苯聚芳醚阴离子交换膜(DEA-QPPEK-OH).采用傅里叶变换红外(FTIR)光谱对制备自交联膜的化学结构进行表征.研究了DETA-QPPEK-OH和DEA-QPPEK-OH膜的理化性质,结果表明前者具有较低吸水率和更低溶胀度.通过研究DETAQPPEK-OH和DEA-QPPEK-OH膜的离子传导率随温度的变化规律,结果表明在80°C时其离子传导率分别达到0.060和0.028 S cm-1,表明本文制备的自交联膜具有较高离子传导率.此外还通过热重分析(TGA)对两类自交联膜的热稳定性进行了研究.
文摘以CO_3^(2-)为检测对象,发展了聚合物敏感膜电位型碳酸根传感器。采用3-辛基噻吩(POT)作为传导层的固体接触式电极技术,通过优化实验条件,构建了聚合物敏感膜CO_3^(2-)选择性电极,该电极对CO_3^(2-)检出限为7.0μmol/L,线性范围为1.0×10^(-5)~1.0×10^(-3)mol/L,能斯特响应斜率为-29.6 m V/decade。传感器已用于海水中CO_3^(2-)的测定。
基金financial supports from the National Key R&D Program of China(No.2019YFC1907801)National Natural Science Foundation of China(No.52174286)+1 种基金Hunan Provincial Science and Technology Plan Project,China(No.2019JJ30031)InnovationDriven of Central South University,China(No.2020CX007)。
文摘The Cu(Ⅱ) separation behaviors with polymer inclusion membranes(PIMs) are explored by modifying 2-aminomethylpyridine derivatives with hydrophobic alkyl chains, including 2-[N-(tert-butyloxycarbonylmethyl)-2-picolyamino]acetate(AMB), N,N-dioctyl-2-aminomethylpyridine(AMD), tert-butyl 2-(N-octyl-2-picolyamino) acetate(AMC), and N,N-didecyl-2-aminomethylpyridine(AME). The transport flux and selectivity of Cu(Ⅱ) are determined by optimizing composition and structure of carriers and plasticizers. The results show that the hydrophobic modification of 2-aminomethylpyridine derivatives can boost the selective transport of copper ions in PIMs and membrane stability. In the optimum composition of 30 wt.% PVC, 30 wt.% AME, and 40 wt.% NPOE, the initial flux of Cu(Ⅱ) is 5.8×10^(−6) mol·m^(−2)·s^(−1). The FT-IR and XPS spectra identify that the alkyl amine functional groups of AME involve in the transport of copper chloride species. The SAXS analysis demonstrates that the generated micro-channels in PIMs induced by the hydrophobic modification of 2-aminomethylpyridine derivatives can contribute to the enhanced Cu(Ⅱ) flux.
文摘Owing to the potential ability of metal nanoparticles to enhance the performance of energy storage devices,their catalytic performance has been studied by many researchers.However,a limited number of suitable characterization techniques does not allow fully elucidating their catalytic mechanism.Herein,high‐accuracy operando magnetometry is employed to investigate the catalytic properties of a cobalt oxide electrode for lithium‐ion batteries fabricated by magnetron sputtering.Using this technique,the magnetic responses generated by the Co‐catalyzed reversible formation and decomposition of a polymer/gel‐like film are successfully detected.A series of CoO/Co films are prepared by magnetron sputtering in different environments at various sputtering times to study the influence of Co content and film thickness on their catalytic properties.It is clearly demonstrated that increasing the Co content enhances the magnetic signal associated with the catalysis process.Furthermore,decreasing the electrode thickness increases the area affected by the catalytic reactions,which in turn enhances the corresponding magnetic responses.The obtained results experimentally confirm the catalytic activity of Co metal nanoparticles and provide a scientific guidance for designing advanced energy storage devices.This work also shows that operando magnetometry is a versatile technique for studying the catalytic effects of transition metals.
基金Projects(51605220,U1637101)supported by the National Natural Science Foundation of ChinaProject(BK20160793)supported by the Jiangsu Provincial Natural Science Foundation,ChinaProject(NS2020029)supported by the Fundamental Research Funds for the Central Universities,China。
文摘In order to further improve the driving performance of ionic polymer metal composites(IPMCs),Nafion/graphene quantum dots(GQDs)hybrid membranes incorporating GQDs with various contents of 0,0.1 wt.%,0.5 wt.%,1.0 wt.%,2.0 wt.%and 4.0 wt.%were fabricated by solution casting,and then IPMCs were manufactured by electroless plating.The water contents and elastic moduli of the hybrid membranes were tested.The morphology characteristics of the hybrid membranes and the IPMCs were observed,and the current,AC impedance,blocking force and displacement of the IPMCs were measured.The results show that the elastic modulus of the hybrid membranes decreases,the water content increases,and the actuation performance of the IPMCs improves significantly after the addition of GQDs.IPMC with 1.0 wt.%GQDs exhibits the best driving property.Compared with the IPMC without GQDs,the working current,ion conductivity,blocking force,and tip displacement increase by 94.67%,311.11%,53.66%,and 66.07%,respectively.These results lay a solid foundation for the preparation of IPMCs with high performance,and further broaden their applications in biomedical devices and bionic robots.
基金Supported by the National Natural Science Foundation of China （20776137） and the National High Technology Research and Develooment Prozram of China （2008AA06Z325）.
文摘In this paper, the effect of hydrogen reduction of silver ions on the performance and structure of new solid polymer electrolyte polyetherimide （PEI）/Pebax2533 （Polynylonl2/tetramethylene oxide block copolymer, PA12-PTMO）/AgBF4 composite membranes is investigated. For PEI/Pebax2533/AgBF4 composite membranesprepared with dillerent AgBF4 concentration, the permeances of propylene and ethylene increase with the increase of AgBF4 concentration due to the carrier-facilitated transport, resulting in a high selectivity. But for propyl- ene/propane mixture, the mixed-gas selectivity is lower than its ideal selectivity. The hydrogen reduction strongly influences the membrane performance, which causes the decrease of propylene permeance and the increase of pro-pane permeance. With the increase of hydrogen reduction time, the membranes show a clearly color change from white to brown, yielding a great selectivity loss. The data of X-ray diffraction and FT-IR prove that silver ions are reduced to Ago after hydrogen reduction, and aggregated on the surface of PEI/Pebax2533/AgBF4 composite mem- branes.
文摘Organic soft actuators are of special interest in many fields including intravascular neurosurgery. Ion conductive polymer film （ICPF） actuators have been one of the strong candidates. The ICPF investigated here was a cation-exchange membrane （Nation 117, Du Pont）. When a voltage is given between the metal eIectrodes of an ICPF actuator, the ICPF actuator bends in the water due to the motion of Li＋ cations with associated water. In order to increase the freedom of the deformation of the ICPF actuator, structures of independent electrode pairs were proposed. The electrodes were selectively deposited by non-electrokvzed plating including the Pt [（NH3）6]^4＋ deposition process in a [Pt（NH3）6]Cl4 solution and the reduction process in a NaBH4 solution. Here, an elastomer adhesive tape with a fine electrode patterns was used performances were reported in detail. as a mask. The actuators processing conditions and their actuator
基金supported by the National Natural Science Foundation of China (21404016)the Key Research Program of Jiangsu Province (BE2017645)+1 种基金the Six Talent Peaks Project of Jiangsu Province (XCL-078)a project funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions of China
文摘In order to effectively improve the properties of anion exchange membrane(AEM)materials,a series of novel poly(aryl ether nitrile)s with flexible side-chain-type quaternary phosphonium cations(PAEN-TPP-x)were designed and prepared on the basis of considering the influences of polymer backbone,cationic group species and the connection way between the cations and polymer chains.The synthetic method,structure and ion-exchange capacity,water absorption,swelling,hydroxide conductivity and alkaline stability of the obtained AEMs were studied.A comparative study with other reported AEMs was also performed for further exploration of the relationship between the structure and properties.These AEMs with flexible side-chain-type quaternary phosphonium cations displayed good comprehensive properties.Their water uptakes and swelling ratios were in the range of 11.6%–22.7%and 4.4%–7.8%at 60℃,respectively.They had hydroxide conductivity in the range of 28.6–45.8 mS cm^-1 at 60℃.Moreover,these AEMs also exhibited improved alkaline stability,and the hydroxide conductivity for PAEN-TPP-0.35 could remain 82.1%and 80.6%of its initial value at 60 and 90℃in 2 mol L^-1 NaOH solution for480 h,respectively.
