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41.
In this paper we describe the experimental analysis of a novel ion-exchange polymer metal composite (IPMC) actuator under
large external voltage. The experimental analysis is supplemented with a coupled thermodynamic model, which includes mass
transport across the thickness of the polymer actuator, chemical reactions at boundaries, and deformation as a function of
the solvent (water) distribution. In this paper, the case of large electrode potentials (over 1.2 V) has been analyzed experimentally
and theoretically. At these voltage levels, electrochemical reactions take place at both electrodes. These are used in the
framework of overpotential theory to develop boundary conditions for the water transport in the bulk of polymer. The model
is then simplified to a three-component system comprised of a fixed negatively charged polymeric matrix, protons, and free
water molecules within the polymer matrix. Among these species, water molecules are considered to be the dominant species
responsible for the deformation of the IPMC actuators. Experiments conducted at different initial water contents are described
and discussed in the context of the proposed deformation mechanism. Comparison of numerical simulations with experimental
data shows good agreement. 相似文献
42.
43.
N.P. Somasiri W.K. Toh X. Chen I.D. Robertson A.A. Rezazadeh 《International Journal of Infrared and Millimeter Waves》2002,23(12):1777-1785
This paper describes numerical modelling of a dual band multi-layered microstrip patch antenna operating at 35GHz on an in-house semi-insulating GaAs substrate. The simulated and measured resonant frequencies at both lower and upper resonant frequencies will be compared to check the accuracy of the different numerical modelling techniques. 相似文献
44.
L. Sauguet B. Ameduri B. Boutevin 《Journal of polymer science. Part A, Polymer chemistry》2006,44(15):4566-4578
The radical terpolymerization of 8‐bromo‐1H,1H,2H‐perfluorooct‐1‐ene with vinylidene fluoride (VDF) and perfluoro(4‐methyl‐3,6‐dioxaoct‐7‐ene) sulfonyl fluoride is presented. Changing the feed compositions of these three fluorinated comonomers enabled us to obtain different random‐type poly[vinylidene fluoride‐ter‐perfluoro(4‐methyl‐3,6‐dioxaoct‐7‐ene) sulfonyl fluoride‐ter‐8‐bromo‐1H,1H,2H‐perfluorooct‐1‐ene] terpolymers containing various sulfonyl fluoride and brominated side groups. Yields higher than 70% were reached in all cases. The hydrolysis of the sulfonyl fluoride group into the ? SO3Li function in the presence of lithium carbonate was quantitatively achieved without the content of VDF being affected, and so dehydrofluorination of the VDF base unit was avoided. These original terpolymers were then crosslinked via dangling bromine atoms in the presence of a peroxide/triallyl isocyanurate system, which produced films insoluble in organic solvents such as acetone and dimethylformamide (which totally dissolved uncured terpolymers). The acidification of ? SO3Li into the ? SO3H function enabled protonic membranes to be obtained. The thermal stabilities of the crosslinked materials were higher than those of the uncured terpolymers, and their electrochemical performances were investigated. According to the contents of the sulfonic acid side functions, the ion‐exchange capacities ranged from 0.6 to 1.5 mequiv of H+/g, whereas the water uptake and conductivities ranged from 5–26% (±11%) and from 0.5 to 6.0 mS/cm, respectively. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4566–4578, 2006 相似文献
45.
The mechanism of the slowly opened Q-switch operation was investigated thoroughly. Maximum energy extraction from the resonator
could be optimized, and the smallest output beam divergence could be achieved. In this article, we present a detailed analysis
that has numerically verified the mode-selection mechanism in the slowly opened Q-switch operation, and the degree of the
smaller output laser beam divergence that has been achieved. The mechanism of the slowly opened Q-switch operation is the
inherent advantage of the passive saturable absorber in this operation. We can use the maximum energy extraction and the smallest
output beam divergence results of the slowly opened Q-switch operation to design and optimize various passive saturable absorbers:
plastic dye sheets, LiF:F2− color center crystals, Cr4+: YAG crystals, RG1000 color glass filters, and the single crystal semiconductor saturable absorber wafers that are in developed
in our microchip laser systems. 相似文献
46.
Yan Yin Otoo Yamada Shunsuke Hayashi Kazuhiro Tanaka Hidetoshi Kita Ken‐Ichi Okamoto 《Journal of polymer science. Part A, Polymer chemistry》2006,44(12):3751-3762
A series of branched/crosslinked sulfonated polyimide (B/C‐SPI) membranes were prepared and evaluated as proton‐conducting ionomers based on the new concept of in situ crosslinking from sulfonated polyimide (SPI) oligomers and triamine monomers. Chemical branching and crosslinking in SPI oligomers with 1,3,5‐tris(4‐aminophenoxy)benzene as a crosslinker gave the polymer membranes very good water stability and mechanical properties under an accelerated aging treatment in water at 130 °C, despite their high ion‐exchange capacity (2.2–2.6 mequiv g?1). The resulting polymer electrolytes displayed high proton conductivities of 0.2–0.3 S cm?1 at 120 °C in water and reasonably high conductivities of 0.02–0.03 S cm?1 at 50% relative humidity. In a single H2/O2 fuel‐cell system at 90 °C, they exhibited high fuel‐cell performances comparable to those of Nafion 112. The B/C‐SPI membranes also displayed good performances in a direct methanol fuel cell with methanol concentrations as high as 50 wt % that were superior to those of Nafion 112. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3751–3762, 2006 相似文献
47.
Nicholas W. DeLuca Yossef A. Elabd 《Journal of Polymer Science.Polymer Physics》2006,44(16):2201-2225
The direct methanol fuel cell (DMFC) has the potential to replace lithium‐ion rechargeable batteries in portable electronic devices, but currently experiences significant power density and efficiency losses due to high methanol crossover through polymer electrolyte membranes (PEMs). Numerous publications document the synthesis and characterization of new PEMs for the DMFC. This article reviews this research, transport phenomena in PEMs, and experimental techniques used to evaluate new PEMs for the DMFC. Although many PEMs do not show significant improvements over Nafion®, the benchmark PEM in DMFCs, experimental results show that several new PEMs exhibit lower methanol crossover at similar proton conductivities and/or higher DMFC power densities. These results and recommendations for future research are discussed. © 2006 Wiley Periodicals, Inc. J Polym Sci Parts B: Polym Phys 44: 2201–2225, 2006 相似文献
48.
Xinyu Huang Roham Solasi Yue Zou Matthew Feshler Kenneth Reifsnider David Condit Sergei Burlatsky Thomas Madden 《Journal of Polymer Science.Polymer Physics》2006,44(16):2346-2357
The life of proton exchange membrane fuel cells (PEMFC) is currently limited by the mechanical endurance of polymer electrolyte membranes and membrane electrode assemblies (MEAs). In this paper, the authors report recent experimental and modeling work toward understanding the mechanisms of delayed mechanical failures of polymer electrolyte membranes and MEAs under relevant PEMFC operating conditions. Mechanical breach of membranes/MEAs in the form of pinholes and tears has been frequently observed after long‐term or accelerated testing of PEMFC cells/stacks. Catastrophic failure of cell/stack due to rapid gas crossover shortly follows the mechanical breach. Ex situ mechanical characterizations were performed on MEAs after being subjected to the accelerated chemical aging and relative humidity (RH) cycling tests. The results showed significant reduction of MEA ductility manifested as drastically reduced strain‐to‐failure of the chemically aged and RH‐cycled MEAs. Postmortem analysis revealed the formation and growth of mechanical defects such as cracks and crazing in the membranes and MEAs. A finite element model was used to estimate stress/strain states of an edge‐constrained MEA under rapid RH variations. Damage metrics for accelerated testing and life prediction of PEMFCs are discussed. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 2346–2357, 2006 相似文献
49.
Baijun Liu Gilles P. Robertson Michael D. Guiver Yi‐Ming Sun Yin‐Ling Liu Juin‐Yih Lai Serguei Mikhailenko Serge Kaliaguine 《Journal of Polymer Science.Polymer Physics》2006,44(16):2299-2310
A series of sulfonated poly(aryl ether ether ketone ketone)s statistical copolymers with high molecular weights were synthesized via an aromatic nucleophilic substitution polymerization. The sulfonation content (SC), defined as the number of sulfonic acid groups contained in an average repeat unit, could be controlled by the feed ratios of monomers. Flexible and strong membranes in sodium sulfonate form could be prepared by the solution casting method, and readily transformed to their proton forms by treating them in 2 N sulfuric acid. The polymers showed high Tgs, which increased with an increase in SC. Membranes prepared from the present sulfonated poly(ether ether ketone ketone) copolymers containing the hexafluoroisopropylidene moiety (SPEEKK‐6F) and copolymers containing the pendant 3,5‐ditrifluoromethylphenyl moiety (SPEEKK‐6FP) had lower water uptakes and lower swelling ratios in comparison with previously prepared copolymers containing 6F units. All of the polymers possessed proton conductivities higher than 1 × 10?2 S/cm at room temperature, and proton conductivity values of several polymers were comparable to that of Nafion at high relative humidity. Their thermal stability, oxidative stability, and mechanical properties were also evaluated. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 2299–2310, 2006 相似文献
50.
A way of determining the flexibility of wood-pulp fibres is developed, which involves i) a precise measurement of the topology
of single-fibres by using a confocal laser scanning microscope and ii) the measurement of the elastic modulus of the fibres
by using a single-fibre fatigue cell. Reported in this paper are the initial results of tests carried out on black spruce
fibres, which have been subjected to three different levels of mechanical refining energy, namely ∼1100, 2300, and 3500 kWh/t.
It is found that the fibre flexibility rises significantly between the first and second energy levels, but it does not change
to the same degree between the second and third ones. The described procedure of measuring the flexibility of fibres may be
used to establish the appropriate refiner energy necessary for the production of a specific grade of paper.
Russian translation published in Mekhanika Kompozitnykh Materialov, Vol. 42, No. 1, pp. 115–128, January–February, 2006. 相似文献