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  • 1
    Online Resource
    Online Resource
    Elsevier BV ; 2001
    In:  Journal of Membrane Science Vol. 185, No. 1 ( 2001-4), p. 3-27
    In: Journal of Membrane Science, Elsevier BV, Vol. 185, No. 1 ( 2001-4), p. 3-27
    Type of Medium: Online Resource
    ISSN: 0376-7388
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2001
    detail.hit.zdb_id: 1491419-0
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    The Electrochemical Society ; 2011
    In:  ECS Transactions Vol. 41, No. 1 ( 2011-10-04), p. 2033-2040
    In: ECS Transactions, The Electrochemical Society, Vol. 41, No. 1 ( 2011-10-04), p. 2033-2040
    Abstract: One theoretical advantage of High Temperature Polymer-Electrolyte Fuel Cells (HT-PEFC) is the higher kinetic of the anode and cathode reaction. Whereas on the anode side the higher kinetic can be achieved practically, the kinetic on the cathode side is in practice lower than in low temperature PEFCs. In this paper different kind of electrode compositions for anode and cathode are prepared to improve the interface between an acid-base blend membrane (Polybenzimidazol-sulfonated Polysulfon) in respect to the cathode kinetic and the ohmic resistance of the Membrane-Electrode-Assembly (MEA).
    Type of Medium: Online Resource
    ISSN: 1938-5862 , 1938-6737
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2011
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  • 3
    Online Resource
    Online Resource
    The Electrochemical Society ; 2015
    In:  ECS Transactions Vol. 69, No. 17 ( 2015-09-14), p. 1075-1087
    In: ECS Transactions, The Electrochemical Society, Vol. 69, No. 17 ( 2015-09-14), p. 1075-1087
    Abstract: Electrochemical Impedance Spectroscopy (EIS) is used to investigate the impact of acid doping level, air stoichiometry, polymer membrane type, and catalyst material on the operation of Membrane Electrode Assemblies (MEA) for high-temperature polymer electrolyte membrane fuel cells (HT-PEMFCs). EIS spectra are recorded during operation and analyzed by means of an equivalent circuit model to separate the contributions of individual internal losses. Acid doping level in membrane and electrodes plays a major role for MEA performance. Air stoichiometry influences the MEA operation mainly by affecting the cathode mass transport and charge transfer losses. The investigated membrane materials have little effect on MEA performance, although differences are observed in the shapes of the EIS spectra. The use of a Pt 3 Co/C alloy catalyst improves the MEA performance to a record value of 707 mV at 200 mA cm -2 in the polarization curve.
    Type of Medium: Online Resource
    ISSN: 1938-5862 , 1938-6737
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2015
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  • 4
    In: Polymers, MDPI AG, Vol. 12, No. 4 ( 2020-04-15), p. 915-
    Abstract: In order to evaluate the performance of the anion exchange membranes in a vanadium redox flow battery, a novel anion exchange polymer was synthesized via a three step process. Firstly, 1-(2-dimethylaminoethyl)-5-mercaptotetrazole was grafted onto poly(pentafluorostyrene) by nucleophilic F/S exchange. Secondly, the tertiary amino groups were quaternized by using iodomethane to provide anion exchange sites. Finally, the synthesized polymer was blended with polybenzimidazole to be applied in vanadium redox flow battery. The blend membranes exhibited better single cell battery performance in terms of efficiencies, open circuit voltage test and charge-discharge cycling test than that of a Nafion 212 membrane. The battery performance results of synthesized blend membranes suggest that those novel anion exchange membranes are promising candidates for vanadium redox flow batteries.
    Type of Medium: Online Resource
    ISSN: 2073-4360
    Language: English
    Publisher: MDPI AG
    Publication Date: 2020
    detail.hit.zdb_id: 2527146-5
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  • 5
    Online Resource
    Online Resource
    The Electrochemical Society ; 2011
    In:  ECS Meeting Abstracts Vol. MA2011-02, No. 16 ( 2011-08-01), p. 1096-1096
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2011-02, No. 16 ( 2011-08-01), p. 1096-1096
    Abstract: Abstract not Available.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2011
    detail.hit.zdb_id: 2438749-6
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  • 6
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2020-01, No. 38 ( 2020-05-01), p. 1646-1646
    Abstract: The core of a PEM water electrolyzer is represented by the proton conductive membrane. While nowadays PFSA-based materials such as Nafion are state of the art in large scale energy applications, there is a strong need for development of cost efficient alternatives, which exhibit reduced gas crossover, high ionic conductivity and durability. Here, we present proton exchange membranes based on two different concepts: Blends of partially fluorinated polybenzimidazole and pyridine side-chain-modified polysulfones ( 3 K-BM) as well as arylene main-chain multiblock co-ionomers (MB-O). The 3 K-BM ionomer membranes represent a blend of hydrophilic partially fluorinated and sulfonated aromatic polyethers with two hydrophobic components: F 6 -PBI and pyridine-modified PSU [1]. Proton conductivity is achieved by the hydrophilic parts of the material whereas the hydrophobic components ensure stability and enable adjustment of mechanical properties. MB-O consists of hydrophobic and hydrophilic building blocks, which are synthesized via step-growth polycondensation. The former blocks are partially fluorinated aromatics, whereas the latter ones are based on sulfonated nonfluorinated aromatics [2]. Multiblock-co-ionomers are capable of forming nanophase-separated structures [2,3], which are tunable by varying the ratio of hydrophilic and hydrophobic proportions. In addition to the polymer synthesis and membrane preparation, ex-situ characterization including NMR spectroscopy, gel permeation chromatography, thermogravimetric analysis, H 2 -crossover analysis via linear-sweep-voltammetry and AC impedance spectroscopy have been performed with our novel materials. First preliminary in-situ tests in a PEM electrolysis cell have already yielded high performances, which can potentially be increased further by optimization of electrodes with respect to binders for the respective membrane material. Acknowledgements This work has been funded by the German Federal Ministry of Education and Research (BMBF) as part of the project: “Increasing Lifespan and Power of Polymer Electrolyte Membrane Electrolysers through High Power Membrane Electrode Assemblies (POWER-MEE)“ References [1] J. Kerres, A. Ullrich, M. Hein, J. Polym. Sci.: Part A: Polym. Chem. 39 (2001) 2874–2888 [2] F. Schönberger, J. Kerres, J.Polym. Sci. Part A: Polym. Chem. 45 (2007) 5237–5255. [3] H. Ghassemi, J. E. McGrath, T. A. Zawodzinski, Polymer 47 (2006) 4132-4139
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2020
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  • 7
    Online Resource
    Online Resource
    The Electrochemical Society ; 2020
    In:  ECS Meeting Abstracts Vol. MA2020-01, No. 38 ( 2020-05-01), p. 1605-1605
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2020-01, No. 38 ( 2020-05-01), p. 1605-1605
    Abstract: In this study, the effect of component composition on the chemical stability of the developed ionic-covalently cross-linked PBI-blended membrane concept from earlier studies for application in SO 2 electrolysis at elevated temperatures ( 〉 100 °C) is further investigated. Three different acid-base ratios were studied by blending a partially fluorinated sulfonated arylene main-chain polymer (SFS) with polybenzimidazole (F 6 PBI) and a partially or non-fluorinated bromo-methylated polymer (BrPAE). In addition two different alkylated imidazoles (EMIm and TMIm) were included as quaternization agents. Accordingly, twelve different PBI-blended membranes were used in this study. The suitability of these membranes for SO 2 electrolysis at elevated temperatures was determined in terms of i) the H 2 SO 4 stability (80 wt% H 2 SO 4 at 100 °C for 120 hours), (ii) the oxidative stability (Fenton’s test, FT) and (iii) the organic solvent stability (extraction in N,N-Dimethylacetamide). Membranes were characterized in terms of the percentage weight, the ion exchange capacity (IEC) and the thermal stability (TGA-FTIR) changes, before and after the various treatments. Although all blended membrane types were sufficiently stable during H 2 SO 4 treatment, proton conductivity measurements indicated that the blends containing only partially fluorinated blend components displayed superior stability (better compatibility) as well as conductivity. Cell voltages showed an improvement of up to 190 mV for operations at 120 °C compared to earlier studies conducted at 80 °C for similar PBI-blended membranes. It was established that both chemically stable and conductive PBI-blended membranes, suitable for SO 2 electrolysis above 100 °C, could be obtained by varying the composition of selected polymer components. Figure 1: Schematic of the ionic-covalently cross-linking concept for the blend membranes (black – BrPAE, purple – F 6 PBI, blue – EMIm, and brown - sPPSU). Figure 1
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2020
    detail.hit.zdb_id: 2438749-6
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  • 8
    Online Resource
    Online Resource
    The Electrochemical Society ; 2020
    In:  ECS Meeting Abstracts Vol. MA2020-01, No. 52 ( 2020-05-01), p. 2927-2927
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2020-01, No. 52 ( 2020-05-01), p. 2927-2927
    Abstract: Alternative energy studies are crucial since the energy demand in the world increases rapidly. Nowadays, due to limited reserves of fossil fuel and CO 2 emission, environmentally green energy is the most promising and desirable energy source for the future. In this context, fuel cells becoming one of the most promising alternative energy conversion devices. Especially polymer electrolyte membrane fuel cells (PEMFCs) are of great research interest. Theoverall efficiency of PEMFCs is strongly influenced by the polymer membrane placed between the anode and cathode. The current state-of-the-art perfluorosulfonic acid (PFSA)-based membranes used in PEMFCs, such as Nafion, rely on the presence of water as the charge carrier for an efficient proton conductivity, and operate usually only up to 80 °C. Therefore, Nafion-based systems require water management, which can be avoided by using polybenzimidazole (PBI)-based membranes instead; operating at higher temperatures (up to 180 °C). Nevertheless, pristine PBI-based membranes need to be doped with acid in order to produce a highly proton conductive system. In this context, phosphoric acid (PA) is the most promising acid as the proton conduction medium. PA doping levels are essential as they govern conductivity, while an excess acid doping can deteriorate mechanical and thermal properties of the membrane. Therefore, the optimization and determination of the doping levels are important for high temperature polymer electrolyte membrane fuel cells. Commonly, titration or weighing of the membranes are used for the determination of the acid doping level, but they suffer from low accuracy and precision. In this work, the acid doping level (ADL) of PBI-based membranes was studied by Raman, impedance, and energy-dispersive X-ray (EDX) spectroscopy, gravimetric and thermogravimetric analysis, and titration. The use of Raman spectroscopy is of great interest due to its non-destructive nature. It can be performed on the sample prior or post application in a HT-PEMFC. This study presents a new measurement protocol for ADLs by using Raman spectroscopy, which is a helpful tool for choosing the optimal ADL for a PBI-based membrane. Thus, the manufacturing process of high temperature fuel cells and their overall efficiency can be optimized. Keywords : Acid Doping Level (ADL), Fuel Cells (FCs), High Temperature (HT), Polymer Electrolyte Membrane (PEM), Phosphoric Acid (PA), Polybenzimidazole (PBI)
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2020
    detail.hit.zdb_id: 2438749-6
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  • 9
    Online Resource
    Online Resource
    The Electrochemical Society ; 2013
    In:  ECS Meeting Abstracts Vol. MA2013-02, No. 15 ( 2013-10-27), p. 1392-1392
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2013-02, No. 15 ( 2013-10-27), p. 1392-1392
    Abstract: Abstract not Available.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2013
    detail.hit.zdb_id: 2438749-6
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  • 10
    Online Resource
    Online Resource
    The Electrochemical Society ; 2018
    In:  ECS Meeting Abstracts Vol. MA2018-01, No. 28 ( 2018-04-13), p. 1601-1601
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2018-01, No. 28 ( 2018-04-13), p. 1601-1601
    Abstract: It has been shown that hydrogen, which can be used for energy storage, can be produced efficiently by the membrane based Hybrid Sulfur (HyS) process. During the HyS electrolysis step, SO 2 and H 2 O are converted to H 2 and H 2 SO 4 . The proton exchange membrane (PEM) used for this process should have both a high proton conductivity and acid stability. Since the widely used perfluorosulfonic type materials are restricted by their humidification requirements, materials such as polybenzimidazole (PBI) has been found to be promising in blends with partially fluorinated polyaromatic polymers at operating temperatures of 80 and 95 °C within the SO 2 electrolyser. Operation at higher temperatures ( 〉 100 °C) however holds many advantages such as improved reaction kinetics and simplified water management. For this study a cross-linked partially fluorinated polyaromatic PBI blended membrane was evaluated at 120 °C. Humidified SO 2 was supplied to the anode to produce sulfuric acid while hydrogen was formed at the cathode. The SO 2 :H 2 O feed was managed at the applied current densities until a constant voltage was obtained, and there after increased accordingly with increasing current density. Polarisation curves (Figure 1) recorded for the blended PBI membrane were comparable with reported s-PBI in literature values in the lower current density region ( 〈 0.5 A/cm 2 ). A maximum current density of 1.1 A/cm 2 was reached in comparison to the 0.5 A/cm 2 for s-PBI at a temperature of 110 °C. Voltage stability was monitored at a current density of 0.3 and 0.6 A/cm 2 for a duration of 6 hours or until the maximum voltage had been reached. The lower current density (0.3 A/cm 2 ) was more constant over the course of the measurement, with a standard deviation of 3 mV, when compared to the higher applied current density. These results are promising for further testing and optimization of the blended PBI membranes for higher temperature SO 2 electrolysis. Figure 1
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2018
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