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Proton Conduction (proton + conduction)
Selected AbstractsInsight into Proton Conduction of Immobilised Imidazole Systems Via Simulations and Impedance Spectroscopy,FUEL CELLS, Issue 3-4 2008W. L. Cavalcanti Abstract The proton conduction in immobilised imidazole systems has been investigated in order to support the design of new membrane materials for polymer electrolyte membrane fuel cells (PEMFC). In the experimental part of this work, proton conductivities are measured via impedance spectroscopy. The simulation and modelling are performed combining molecular dynamics simulations and energy barrier calculations; the analysis is done via the proton jump energy barrier, collision ratio and radial distribution function. The dependence of the proton mobility on the temperature, spacer length and the density of conducting groups per area is presented. Donors and acceptors groups approach to each other within a distance from 2.8 to 3,Å where the energy barrier for a proton transfer is very low, which favours the proton jump under the studied conditions. The proton conductivity increases with increase in the spacer length. The simulation results are in good agreement with the proton conductivities presented. [source] Sulfonated polybenzimidazoles: Proton conduction and acid,base crosslinkingJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 16 2010Owen D. Thomas Abstract A series of soluble, benzimidazole-based polymers containing sulfonic acid groups (SuPBI) has been synthesized. SuPBI membranes resist extensive swelling in water but are poor proton conductors. When blended with high ion exchange capacity (IEC) sulfonated poly(ether ether ketone) (SPEEK), a polymer that has high proton conductivity but poor mechanical integrity, ionic crosslinks form reducing the extent of swelling. The effect of sulfonation of PBI on crosslinking in these blends was gauged through comparison with nonsulfonated analogs. Sulfonic acid groups present in SuPBI compensate for acid groups involved in crosslinking, thereby increasing IEC and proton conductivity of the membrane. When water uptake and proton conductivity were compared to the IEC of blends containing either sulfonated or nonsulfonated PBI, no noticeable distinction between PBI types could be made. Comparisons were also made between these blends and pure SPEEK membranes of similar IEC. Blend membranes exhibit slightly lower maximum proton conductivity than pure SPEEK membranes (60 vs. 75 mS cm,1) but had significantly enhanced dimensional stability upon immersion in water, especially at elevated temperature (80 °C). Elevated temperature measurements in humid environments show increased proton conductivity of the SuPBI membranes when compared with SPEEK-only membranes of similar IEC (c.f. 55 for the blend vs. 42 mS cm,1 for SPEEK at 80 °C, 90% relative humidity). © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3640,3650, 2010 [source] Microstructural Engineering of Hydroxyapatite Membranes to Enhance Proton ConductivityADVANCED FUNCTIONAL MATERIALS, Issue 24 2009Dongxia Liu Abstract A new approach to enhancing proton conductivity of ceramics is demonstrated by aligning proton conductive pathways and eliminating resistive grain boundaries. Hydroxyapatite (HAP) membranes are synthesized by multistage crystallization onto palladium. The synthesis involves three steps: electrochemical deposition of HAP seeds, secondary hydrothermal crystallization onto the seed layer to promote c -axis growth normal to the substrate, and tertiary hydrothermal crystallization to promote a- axis growth to fill the gaps between the aligned crystals. The c -axis alignment with crystal domains spanning the membrane thickness significantly enhances proton conduction since protons are primarily transported along the c -axes of HAP crystals. The novel HAP membranes display proton conductivity almost four orders of magnitude higher than traditional sintered HAP ceramics. The HAP membranes on palladium hydrogen membrane substrates hold promise for use in intermediate-temperature fuel cells, chemical sensors, and other devices. The synthesis approach presented may also be applied to other ion-conducting membrane materials to enhance transport properties. [source] Periodicity in proton conduction along a H-bonded chain.INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, Issue 3 2008Application to biomolecules Abstract Molecular complexes are constructed to simulate proton transfer channels of the influenza A virus and of the active site of carbonic anhydrase. These complexes consist of proton donor and acceptor groups connected by a chain of water molecules. Quantum chemical calculations on the methylimidazole(H+)H2OCH3COO, model of the M2 virus channel indicate free translational motion of the water molecule between donor and acceptor, as well as concerted transfer of both H-bond protons. The proton transfer barrier does not depend on the position of the bridged water molecule and varies linearly with the difference of electrostatic potentials between the donor and acceptor. When the water chain is elongated, and with various donor and acceptor models, periodicity appears in the H-bond lengths and the progression of proton transfer in each link. This "wave" is shown to propagate along the chain, as it is driven by the displacement of a single proton. One can thereby estimate the velocity of the proton wave and proton conduction time. Computations are performed to examine the influence of immersing the system within a polarizable medium. © 2007 Wiley Periodicals, Inc. Int J Quantum Chem, 2008 [source] Preparation and conductivity of substituted germanic heteropoly acids polyethylene glycol hybrid materialsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2008Shouli Zhao Abstract In this work, the polyethylene glycol (PEG) hybrid materials composited with substituted germanic heteropoly acids were prepared. Infrared (IR) spectra revealed that the Keggin structure characteristic of the GeM11VO405, anion were present in the hybrid materials. At room temperature (20°C), the conductivity of the products is 4.07 × 10,3 S cm,1 and 2.12 × 10,3 S cm,1, respectively. The results indicated that the conductivity of substituted germanic heteropoly acids PEG hybrid materials is higher than that of the corresponding pure substituted germanic heteropoly acids. According to the experimental results, we proposed a possible mechanism of the proton conduction of the hybrid materials. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Proton transportation in an organic,inorganic hybrid polymer electrolyte based on a polysiloxane/poly(allylamine) networkJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 15 2005Ping-Lin Kuo Abstract A new class of proton-conducting polymer was developed via the sol,gel process from amino-containing organic,inorganic hybrids by the treatment of poly(allylamine) with 3-glycidoxypropyltrimethoxysilane doped with ortho -phosphoric acid. The polymer matrix contains many hydrophilic sites and consists of a double-crosslinked framework of polysiloxane and amine/epoxide. Differential scanning calorimetry results suggest that hydrogen bonding or electrostatic forces are present between H3PO4 and the amine nitrogen, resulting in an increase in the glass-transition temperature of the poly(allylamine) chain with an increasing P/N ratio. The 31P magic-angle spinning NMR spectra indicate that three types of phosphate species are involved in the proton conduction, and the motional freedom of H3PO4 is increased with increasing P/N ratios. The conductivity above 80 °C does not drop off but increases instead. Under a dry atmosphere, a high conductivity of 10,3 S/cm at temperatures up to 130 °C has been achieved. The maximum activation energy obtained at P/N = 0.5 suggests that a transition of proton-conducting behavior exits between Grotthus- and vehicle-type mechanisms. The dependence of conductivity on relative humidity (RH) above 50% is smaller for H3PO4 -doped membranes compared with H3PO4 -free ones. These hybrid polymers have characteristics of low water content (23 wt %) and high conductivity (10,2 S/cm at 95% RH), making them promising candidates as electrolytes for fuel cells. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 3359,3367, 2005 [source] Sulfonated naphthalene dianhydride based polyimide copolymers for proton-exchange-membrane fuel cells.JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 4 2004Abstract A novel sulfonated diamine, 3,3,-disulfonic acid-bis[4-(3-aminophenoxy)phenyl]sulfone (SA-DADPS), was prepared from m -aminophenol and disodium-3,3,-disulfonate-4,4,-dichlorodiphenylsulfone. The conditions necessary to synthesize and purify SA-DADPS in high yields were investigated in some detail. This disulfonated aromatic diamine, containing ether and sulfone linkages, was used to prepare N -methyl-2-pyrrolidinone-soluble, six-membered ring polyimide copolymers containing pendent sulfonic acid groups by a catalyzed one-step high-temperature polycondensation in m -cresol. These materials showed much improved hydrolytic stability with respect to phthalimides. High-molecular-weight film-forming statistical copolymers with controlled degrees of disulfonation were prepared through variations in the stoichiometric ratio of disulfonated diamine (SA-DADPS) in its soluble triethylamine salt form to several unsulfonated diamines. Three unsulfonated diamines, bis[4-(3-aminophenoxy)phenyl] sulfone, 4,4,-oxydianiline, and 1,3-phenylenediamine, were used to prepare the copolymers. The characterization of the copolymers by 1H NMR, Fourier transform infrared, ion-exchange capacity, and thermogravimetric analysis demonstrated that SA-DADPS was quantitatively incorporated into the copolymers. Solution-cast films of the sulfonated copolymers were prepared and afforded tough, ductile membranes with high glass-transition temperatures. Methods were developed to acidify the triethylammonium salt membranes into their disulfonic acid form, this being necessary for proton conduction in a fuel cell. The synthesis and characterization of these materials are described in this article. Future articles will describe the performance of these copolymers as proton-exchange membranes in hydrogen/air and direct methanol fuel cells. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 862,874, 2004 [source] Electrical Conductivity of the High-Temperature Proton Conductor BaZr0.9Y0.1O2.95JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 4 2000Hans G. Bohn The impedance of the cubic perovskite BaZr0.9Y0.1O3-, has been systematically investigated in dry and wet atmospheres at high and low oxygen partial pressures. In the grain interior, conductivity contributions from oxygen ions, electron holes, and protons can be identified. Below 300°C, proton conduction dominates and increases linearly with the frozen-in proton concentration. The proton mobility, with an activation energy of 0.44 ± 0.01 eV is among the highest ever reported for a perovskite-type oxide proton conductor. For dry oxygen atmos-pheres, electron hole conduction dominates with an activation energy of ,0.9 eV. At temperatures <500°C, the grain-boundary conductivity can be separated and increases upon incorporation of protons. The high electrical conductivity and chemical stability make acceptor-doped barium zirconate a good choice for application as a high-temperature proton conductor. [source] Solvate-Supported Proton Transport in ZeolitesCHEMPHYSCHEM, Issue 4 2004Marion E. Franke Dr. Abstract Solvate-supported proton transport in zeolite H-ZSM-5 was studied by means of complex impedance spectroscopy. The zeolite shows enhanced proton mobility in the presence of NH3and H2O that depends on the concentration of the solvate molecule, temperature (298,773 K), and the SiO2/Al2O3ratio of the zeolite (30,1000). In general, proton conductivity in H-ZSM-5 is most effectively supported in the presence of NH3and H2O at high concentrations, low temperatures, and low SiO2/Al2O3ratios (,80). For the aluminum-rich samples desorption measurements reflect different transport mechanisms that depend on the respective temperature range. Up to about 393 K a Grotthus-like proton transport mechanism is assumed, whereas at higher temperatures (393,473 K) vehiclelike transport seems to dominate. The activation energies for NH4+and H3O+vehicle conductivity depend on the SiO2/Al2O3ratio, and the values are in the range of 49,59 and 39,49 kJ,mol,1, respectively, and thus significantly lower than those for "pure" proton conduction in solvate-free samples. [source] | |||||||||||||