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Ion Exchange Capacity (ion + exchange_capacity)
Selected AbstractsSulfonated poly(phenylene oxide) membranes as promising materials for new proton exchange membranesPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 5 2006Shifang Yang Abstract Poly(phenylene oxide) (PPO) was sulfonated to different ion exchange capacities (IECs) using chlorosulfonic acid as the sulfonating agent. Tough, ductile films were successfully cast from sulfonated PPO (SPPO) solutions in N -methyl-2-pyrrolidone or N,N -dimethylformamide. The obtained membranes had good thermal stability revealed by thermogravimetric analysis (TGA). Compared with an unsulfonated PPO membrane, the hydrophilicity and water uptake of the SPPO membranes were enhanced, as shown by reduced contact angles with water. The tensile test indicated that the SPPO membranes with IEC ranging from 0.77 to 2.63,meq/g were tough and strong at ambient conditions and still maintained adequate mechanical strength after immersion in water at room temperature for 24,hr. The results of wide-angle X-ray diffraction (WAXD) showed amorphous structures for PPO and SPPO while the peak intensity decreased after sulfonation. The proton conductivity of these SPPO membranes was measured as 1.16,×,10,2,S/cm at ambient temperature, which is comparable to that of Nafion 112 at similar conditions and in the range needed for high-performance fuel cell proton exchange membranes. Copyright © 2006 John Wiley & Sons, Ltd. [source] Synthetic Strategies for Controlling the Morphology of Proton Conducting Polymer Membranes,,FUEL CELLS, Issue 2 2005Y. Yang Abstract The nanostructure and morphology of proton conducting polymers is of considerable interest in the search for next generation materials and optimization of existing ones. Synthetic methodologies for tailoring molecular structures that promote nanoscopic phase separation of ionic and non-ionic domains, and the effect of phase separation on parameters such as proton conductivity, are considered. Rather than distinguish proton conducting polymers according to chemical class, they are categorized under sub-headings of random, block, and graft copolymers. The synthetic methodology available to access archetypal polymer structures is dependent on the nature of the monomers and restrictive compared to conventional non-ionic polymer systems. Irrespective of the methodology, ionic aggregation and phase separation are consistently found to play an important role in the proton conductivity of low ion exchange capacity,(IEC) membranes, but less of a role in high IEC membranes. Significant research is required to further develop relationships between polymer architecture, morphology, and electrolytic properties. [source] Polymer electrolyte membranes having sulfoalkyl grafts into ETFE film prepared by radiation-induced copolymerization of methyl acrylate and methyl methacrylateJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2009Truong Thi Hanh Abstract Polymer electrolyte membranes (PEMs) containing alkylsulfonic acid grafts can be prepared by radiation-induced graft copolymerization of methyl acrylate (MA) and methyl methacrylate (MMA) into a poly(ethylene- co -tetrafluoroethylene) film followed by sulfonation of the MA units in the copolymer grafts using an equimolar complex of chlorosulfonic acid and 1,4-dioxane (ClSO3H-Complex). PEMs with MA/MMA copolymer grafts that are 33%,79% MA units were prepared by preirradiation with a dose of 20 kGy and grafting in bulk comonomers at 60°C. The grafted films are treated with ClSO3H-Complex to obtain PEMs with ion exchange capacity of 0.36-0.81 mmol/g (sulfonation degrees of 20%,40%) and proton conductivity of 0.04-0.065 S/cm. These values can be controlled by changing the MA content the sulfonation occurring at an ,-carbonyl carbon. The PEMs with higher MMA content showed higher durability in water (80°C) and under oxidative conditions (3% H2O2) at 60°C. This is because the PMMA grafts in the PEMs have no proton at an ,-carbonyl carbon, which is considered to be a trigger of the degradation of grafting polymers. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Cation exchange finishing of nonwoven polyester with polycarboxylic acids and cyclodextrinsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007L. Ducoroy Abstract We describe a chemical method for the finishing of polyester nonwoven fabrics that aimed to obtain ion exchange textiles. This approach was based on the use of polycarboxylic acids (PCA) and cyclodextrins as carbohydrate compounds and finishing agents, respectively. It was observed that the reaction between these reactants yielded a crosslinked polymer that was physically anchored onto the fibers. This polymer can be considered as a resin issued from the esterification between the COOH groups of the PCA with the OH groups of the carbohydrate. As the esterification reaction was not complete, many free carboxylic groups remained on the surface of the coating polymer. This feature offered the ion exchange properties to the textile support. In this article, we described the pad-dry-cure process and showed the influence of the curing parameters (time and temperature), the nature, and the concentration of the components and the pH of the impregnating bath. The grafting rate (in wt %) and the ion exchange capacity (IEC) were observed in parallel. First, it was observed that the best IEC capacity (that could reach 1 mmol/g) was obtained when an ideal compromise was applied between time and temperature of curing. We also evidenced that IEC depended on the nature and on the concentration of the PCA (chosen among citric acid, 1,2,3,4-butanetetracarboxylic acid, and polyacrylic acid) and on the pH of the impregnating bath. Finally, it was observed that cyclodextrins were more appropriate than starch as finishing coreactants. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3730,3738, 2007 [source] Ammonia exchange on clinoptilolite from mineral deposits located in MexicoJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 6 2004Roberto Leyva-Ramos Abstract This work investigated the ion exchange of ammonia on clinoptilolite obtained from mineral deposits located in San Luis Potosi and Sonora, Mexico. Experimental ion exchange isotherm data were obtained in a batch adsorber. The effects of temperature and solution pH on the ion exchange capacity were studied and it was found that the exchange capacity was slightly increased by augmenting the temperature and by decreasing the pH from 6 to 3. The ion exchange capacity was independent of the diameter of the zeolite particles. The reversibility of ion exchange was analyzed by desorbing the ammonia exchanged on the zeolite. The ion exchange was reversible when 1% NaCl solution was used as the desorbing solution, but more ammonia was desorbed using 1% KCl solution in the desorption step. It was concluded that a considerable amount of ammonia was exchanged on the clinoptilolite and that the exchange capacity was slightly dependent on the temperature and pH. Copyright © 2004 Society of Chemical Industry [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] Sulfonated poly(ether sulfone)s with binaphthyl units as proton exchange membranes for fuel cell applicationJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 21 2009Kazuya Matsumoto Abstract Sulfonated poly(ether sulfone)s containing binaphthyl units (BNSHs) were successfully prepared for fuel cell application. BNSHs, which have very simple structures, were easily synthesized by postsulfonation of poly(1,1,-dinaphthyl ether phenyl sulfone)s and gave tough, flexible, and transparent membranes by solvent casting. The BNSH membranes showed low water uptake compared to a typical sulfonated poly(ether ether sulfone) (BPSH-40) membrane with a similar ion exchange capacity (IEC) value and water insolubility, even with a high IEC values of 3.19 mequiv/g because of their rigid and bulky structures. The BNSH-100 membrane (IEC = 3.19 mequiv/g) exhibited excellent proton conductivity, which was comparable to or even higher than that of Nafion 117, over a range of 30,95% relative humidity (RH). The excellent proton conductivity, especially under low RH conditions, suggests that the BNSH-100 membrane has excellent proton paths because of its high IEC value, and water insolubility due to the high hydrophobicity of the binaphthyl structure. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 5827,5834, 2009 [source] Synthesis and characterization of sulfonated-fluorinated, hydrophilic-hydrophobic multiblock copolymers for proton exchange membranesJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 4 2009Xiang Yu Abstract Hydrophilic/hydrophobic block copolymers as proton exchange membranes (PEMs) has become an emerging area of research in recent years. These copolymers were obtained through moderate temperature (, 100 °C) coupling reactions, which minimize the ether-ether interchanges between hydrophobic and hydrophilic telechelic oligomers via a nucleophilic aromatic substitution mechanism. The hydrophilic blocks were based on the nucleophilic step polymerization of 3,3,-disulfonated, 4,4,-dichlorodiphenyl sulfone with an excess 4,4,-biphenol to afford phenoxide endgroups. The hydrophobic (fluorinated) blocks were largely based on decafluoro biphenyl (excess) and various bisphenols. The copolymers were obtained in high molecular weights and were solvent cast into tough membranes, which had nanophase separated hydrophilic and hydrophobic regions. The performance and structure-property relationships of these materials were studied and compared to random copolymer systems. NMR results supported that the multiblock sequence had been achieved. They displayed superior proton conductivity, due to the ionic proton conducting channels formed through the self-assembly of the sulfonated blocks. The nano-phase separated morphologies of the copolymer membranes were studied and confirmed by atomic force microscopy. Through control of a variety of parameters, including ion exchange capacity and sequence lengths, performances as high, or even higher than those of the state-of-the-art PEM, Nafion, were achieved. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1038,1051, 2009 [source] Structure,property correlations of sulfonated polyimides.JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 14 2004Abstract A series of six-membered sulfonated polyimides were synthesized using 1,4,5,8-naphthalenetetracarboxylic dianhydride, 4,4,-diaminobiphenyl 2,2,-disulfonic acid as the sulfonated diamine, and various nonsulfonated diamine monomers having different bridging groups. These bulky bridging groups have the capacity to increase hydrolytic stability and proton conductivity. Polyimides with bulky bridging groups showed increased solubility but exhibited lower thermal stability. The ion exchange capacity and water uptake reduced with increase in the bulkiness of the bridging group. This was attributed to the increase in the molecular weight of the repeating unit and hence effectively reduced the sulfonic acid content. In low temperatures, the conductivity was lower than Nafion®115 and, with increase in temperature, the conductivity rapidly increased and exhibited better conductivity than Nafion®115. Polyimides with bulky bridging groups 4-amino phenyl sulfone, and 2-bis[4-(4-aminophenoxy)phenyl]hexafluoropropane showed higher conductivity than other polyimides and Nafion®115 despite low ion exchange capacity. The hydrolytic stability of the polyimides with bulky bridging groups was higher than the polyimides with less bulky atoms because of the imparted flexibility. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 3612,3620, 2004 [source] Low Water Swelling and High Proton Conducting Sulfonated Poly(arylene ether) with Pendant Sulfoalkyl Groups for Proton Exchange MembranesMACROMOLECULAR RAPID COMMUNICATIONS, Issue 24 2007Jinhui Pang Abstract Novel side-chain-type sulfonated poly(arylene ether) with pendant sulfoalkyl group copolymers (PSA-SPAE-6F) have been synthesized by direct copolymerization from a new sulfonated monomer, sodium 3-(4-(2,6-difluorobenzoyl)phenyl)propane-1-sulfonate. The sulfonate content could be easily controlled by adjusting the sulfonated and the unsulfonated monomer feed ratio. The obtained copolymers all show good thermal and mechanical properties. It should be noted that the most highly sulfonated copolymer, PSA-SPAE-6F90 with an ion exchange capacity of 1.30 mequiv,·,g,1, shows a proton conductivity of 0.11 S,·,cm,1 and a water swelling ratio of only 12.9% at 100,°C, which indicates its high proton conductivity and excellent dimensional stability in hot water. [source] Partially Sulfonated Polystyrene and Poly(2,6-dimethyl-1,4-phenylene oxide) Blend Membranes for Fuel CellsMACROMOLECULAR RAPID COMMUNICATIONS, Issue 13 2004Bokyung Kim Abstract Summary: Based on Flory,Huggins parameters (,), the miscibility and the effect of morphological change on proton conductivity and methanol permeability of partially sulfonated polystyrene (SPS) and partially sulfonated poly(2,6-dimethyl-1,4-phenylene oxide) (SPPO), having an identical ion exchange capacity, were investigated. When 50 wt.-% of SPPO was blended, both the proton conductivity and methanol permeability had the highest values, which resulted from the change of amorphous domains and the hydrogen bonding between the two ionomers. The proton conductivities, water uptake and methanol permeability for the SPPO/SPS blend membranes studied here. The membranes with 50 wt.-% SPPO clearly showed the greatest increase in these properties. [source] Proton conducting membranes based on poly(vinyl chloride) graft copolymer electrolytesPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 7 2008Jin Kyu Choi Abstract The direct preparation of proton conducting poly(vinyl chloride) (PVC) graft copolymer electrolyte membranes using atom transfer radical polymerization (ATRP) is demonstrated. Here, direct initiation of the secondary chlorines of PVC facilitates grafting of a sulfonated monomer. A series of proton conducting graft copolymer electrolyte membranes, i.e. poly(vinyl chloride)- g -poly(styrene sulfonic acid) (PVC- g -PSSA) were prepared by ATRP using direct initiation of the secondary chlorines of PVC. The successful syntheses of graft copolymers were confirmed by 1H-NMR and FT-IR spectroscopy. The images of transmission electron microscopy (TEM) presented the well-defined microphase-separated structure of the graft copolymer electrolyte membranes. All the properties of ion exchange capacity (IEC), water uptake, and proton conductivity for the membranes continuously increased with increasing PSSA contents. The characterization of the membranes by thermal gravimetric analysis (TGA) also demonstrated their high thermal stability up to 200°C. The membranes were further crosslinked using UV irradiation after converting chlorine atoms to azide groups, as revealed by FT-IR spectroscopy. After crosslinking, water uptake significantly decreased from 207% to 84% and the tensile strength increased from 45.2 to 71.5,MPa with a marginal change of proton conductivity from 0.093 to 0.083,S,cm,1, which indicates that the crosslinked PVC- g -PSSA membranes are promising candidates for proton conducting materials for fuel cell applications. Copyright © 2008 John Wiley & Sons, Ltd. [source] Preparation of new membranes based on sulfonated aromatic copolyimidesPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 5 2008Ahmad Rabiee Abstract New sulfonated aromatic copolyimides with controlled degree of sulfonation were prepared via polycondensation reactions of a sulfonated diamine and two unsulfonated diamines with 1,4,5,8-naphthalene tetracarboxylic dianhydride (NDA). The sulfonated diamine 3,3,-disulfonic acid- bis[4-(5-amino-1-naphthoxy)phenyl]sulfone (DANPS) was synthesized through nucleophilic substitution reaction of 5-amino-1-naphthol with disodium-3,3,-disulfonate-4,4,-dichlorodiphenysulfone (SDCDPS) and subsequent acidification. Two unsulfonated diamines 4,4,-(5-amino-1-naphthoxy)diphenylsulfone (ANDS) and 4,4,-(4-aminophenoxy)diphenylsulfone (APDS) were prepared by nucleophilic reaction of 5-amino-1-naphthol and 4-aminophenol with 4,4,-dichlorodiphenylsulfone in the presence of potassium carbonate, respectively. After characterization of the monomers and polymers with common methods, the physical properties of the polymers including thermal behavior and stability, viscosity, molecular weight, and ion exchange capacity (IEC) were studied. The polymers showed high thermal stability and ion exchange capacity which were the basic requirements for application as fuel cell membranes. Copyright © 2008 John Wiley & Sons, Ltd. [source] Effect of sulfonic group on solubility parameters and solubility behavior of poly(2,6-dimethyl-1,4-phenylene oxide)POLYMERS FOR ADVANCED TECHNOLOGIES, Issue 1 2007Chunli Gong Abstract An investigation on the effect of sulfonic group on solubility parameters and solubility behavior of poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) is presented. Sulfonated PPO (SPPO) was prepared using chlorosulfonic acid as a sulfonating agent. The structure of SPPO was confirmed by FT-IR, and the ion exchange capacity (IEC) of SPPO was accurately determined by conductometric titration and 1H-NMR. The three-dimensional solubility parameters of SPPO defined by Hansen were estimated by group contribution, and this approach was used to obtain the three coordinates of a solubility parameter in terms of: a dispersion part ,d, a polar part ,p and a hydrogen bonding part ,h. The theoretical predications of solubility behavior were characterized using "soluble sphere" in three-dimensional space. The estimated results were in accordance with the solubility experiments in different solvents. Copyright © 2006 John Wiley & Sons, Ltd. [source] | |||||||||||||