33 research outputs found

    Aliphatic anion exchange ionomers with long spacers and no ether links by Ziegler–Natta polymerization: properties and alkaline stability

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    In this work we report the synthesis of poly(vinylbenzylchloride-co-hexene) copolymer grafted with N,N-dimethylhexylammonium groups to study the effect of an aliphatic backbone without ether linkage on the ionomer properties. The copolymerization was achieved by the Ziegler– Natta method, employing the complex ZrCl4 (THF)2 as a catalyst. A certain degree of crosslinking with N,N,N0,N0-tetramethylethylenediamine (TEMED) was introduced with the aim of avoiding excessive swelling in water. The resulting anion exchange polymers were characterized by 1H-NMR, FTIR, TGA, and ion exchange capacity (IEC) measurements. The ionomers showed good alkaline stability; after 72 h of treatment in 2MKOH at 80 C the remaining IEC of 76% confirms that ionomers without ether bonds are less sensitive to a SN2 attack and suggests the possibility of their use as a binder in a fuel cell electrode formulation. The ionomers were also blended with polyvinyl alcohol (PVA) and crosslinked with glutaraldehyde. The water uptake of the blend membranes was around 110% at 25 C. The ionic conductivity at 25 C in the OH form was 29.5 mS/cm

    Anion-conducting polymer electrolyte without ether linkages and with ionic groups grafted on long side chains: Poly(Alkylene Biphenyl Butyltrimethyl Ammonium) (ABBA)

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    In thisworkwe report the synthesis of the newionomer poly(alkylene biphenyl butyltrimethyl ammonium) (ABBA) with a backbone devoid of alkaline-labile C-O-C bonds and with quaternary ammonium groups grafted on long side chains. The ionomer was achieved by metalation reaction with n-butyllithium of 2-bromobiphenyl, followed by the introduction of the long chain with 1,4-dibromobutane. The reaction steps were followed by 1H-NMR spectroscopy showing the characteristic signals of the Br-butyl chain and indicating the complete functionalization of the biphenyl moiety. The precursor was polycondensed with 1,1,1-trifluoroacetone and then quaternized using trimethylamine (TMA). After the acid catalyzed polycondensation, the stoichiometric ratio between the precursors was respected. The quaternization with TMA gave a final degree of amination of 0.83 in agreement with the thermogravimetric analysis and with the ion exchange capacity of 2.5 meq/g determined by acid–base titration. The new ionomer blended with poly(vinylalcohol) (PVA) or poly(vinylidene difluoride) (PVDF) was also characterized by water uptake (WU) and ionic conductivity measurements. The higher water uptake and ionic conductivity observed with the PVDF blend might be related to a better nanophase separation

    Prodromal angina and risk of 2-year cardiac mortality in patients with ST-segment elevation myocardial infarction undergoing primary percutaneous intervention

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    We sought to investigate the prognostic significance of prodromal angina (PA) in unselected patients with ST-segment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PPCI) and its additive predictive value to the GRACE score.We prospectively enrolled 3015 consecutive STEMI patients undergoing PPCI. Patients were divided in 2 groups according to the presence or absence of PA. Multivariable Cox regression was used to establish the relation to 2-year cardiac mortality of PA.The mean age of the study population was 68 (±14) years; 2178 patients (72%) were male. During follow-up, 395 (13%) patients died with 278 of these (9.2%) suffering from cardiac mortality. Kaplan-Meier estimates showed a survival rate of 95% and 87% for patients with PA and no PA, respectively (log rank test < 0.001). After multivariable analysis, patients with PA had still a lower risk of 2 years' cardiac mortality compared with patients without PA (adjusted hazard ratio = 0.50; 95% confidence interval [CI] 1.06-1.81, P = .001). Evaluation of net reclassification improvement showed that reclassification improved by 0.16% in case patients, whereas classification worsened in control patients by 1.08% leading to a net reclassification improvement of -0.93% (95% CI: -0.98, -0.88).In patients with STEMI undergoing PPCI the presence of PA is independently associated with a lower risk of 2-year cardiac mortality. However, the incorporation of this variable to the GRACE score slightly worsened the classification of risk. Accordingly, it seems unlikely that the evaluation of PA may be useful in clinical practice

    Ion conducting membranes for fuel cells

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    Dans cette thèse, les membranes perfluorosulfoniques (PFSA) et les polymères aromatiques sulfonés (SAP) sont étudiés en vue d'une meilleure compréhension de leurs propriétés thermodynamiques, d'hydratation, mècaniques et électriques.Concernant les PFSA: 1) Préparation de membranes Nafion ayant diverses morphologies et structures (amorphe, semi-cristalline, stratifiée) et relation avec les propriétés, comme la transition vitreuse, la fusion, la conductivité protonique. 2) Divers traitements de recuit ont été appliqués et analysés par une nouvelle méthode quantitative appelé INCA (Ionomère nc analyse), utilisant aussi des agents de recuit spéciaux. Concernant les SAP: 1) Synthèse in situ de polymères réticulés et clarification du mécanisme. 2) Optimisation du degré de reticulation en vue de la meilleure conductivité protonique. 3) Obtention d'ionomères conducteurs cationiques par échange de cations du SPEEK et détermination des propriétés de ces nouveaux ionomères.In this thesis, perfluorosulfonic acid membranes (PFSA) and sulfonated aromatic polymers (SAP) are studied to better understandtheir thermodynamic, hydration, mechanical and electrical properties. The following main points were addressed:Regarding PFSA:1) Nafion membranes with various morphology and microstructure (amorphous, semi-crystalline, layered) were prepared and the relation to the properties, such as glass and melting transitions, and proton conductivity, was established.2) Various annealing treatments were performed and analyzed by the quantitative INCA (Ionomer nc Analysis) method using also special annealing agents. Regarding SAP:1) The in situ synthesis of cross-linked polymers was studied and the mechanism was clarified. 2) The degree of cross-linking was optimized for best proton conductivity.3) Cation-conducting ionomers were obtained by cation exchange of SPEEK and the properties of these new ionomers were determined

    Anion-Conducting Polymer Electrolyte without Ether Linkages and with Ionic Groups Grafted on Long Side Chains: Poly(Alkylene Biphenyl Butyltrimethyl Ammonium) (ABBA)

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    In this work we report the synthesis of the new ionomer poly(alkylene biphenyl butyltrimethyl ammonium) (ABBA) with a backbone devoid of alkaline-labile C-O-C bonds and with quaternary ammonium groups grafted on long side chains. The ionomer was achieved by metalation reaction with n-butyllithium of 2-bromobiphenyl, followed by the introduction of the long chain with 1,4-dibromobutane. The reaction steps were followed by 1H-NMR spectroscopy showing the characteristic signals of the Br-butyl chain and indicating the complete functionalization of the biphenyl moiety. The precursor was polycondensed with 1,1,1-trifluoroacetone and then quaternized using trimethylamine (TMA). After the acid catalyzed polycondensation, the stoichiometric ratio between the precursors was respected. The quaternization with TMA gave a final degree of amination of 0.83 in agreement with the thermogravimetric analysis and with the ion exchange capacity of 2.5 meq/g determined by acid–base titration. The new ionomer blended with poly(vinylalcohol) (PVA) or poly(vinylidene difluoride) (PVDF) was also characterized by water uptake (WU) and ionic conductivity measurements. The higher water uptake and ionic conductivity observed with the PVDF blend might be related to a better nanophase separation

    Silica Containing Composite Anion Exchange Membranes by Sol–Gel Synthesis: A Short Review

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    International audienceThis short review summarizes the literature on composite anion exchange membranes (AEM) containing an organo-silica network formed by sol-gel chemistry. The article covers AEM for diffusion dialysis (DD), for electrochemical energy technologies including fuel cells and redox flow batteries, and for electrodialysis. By applying a vast variety of organically modified silica compounds (ORMOSIL), many composite AEM reported in the last 15 years are based on poly (vinylalcohol) (PVA) or poly (2,6-dimethyl-1,4-phenylene oxide) (PPO) used as polymer matrix. The most stringent requirements are high permselectivity and water flux for DD membranes, while high ionic conductivity is essential for electrochemical applications. Furthermore, the alkaline stability of AEM for fuel cell applications remains a challenging problem that is not yet solved. Possible future topics of investigation on composite AEM containing an organo-silica network are also discussed

    Anion Exchange Membranes with 1D, 2D and 3D Fillers: A Review

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    International audienceHydroxide exchange membrane fuel cells (AEMFC) are clean energy conversion devices that are an attractive alternative to the more common proton exchange membrane fuel cells (PEMFCs), because they present, among others, the advantage of not using noble metals like platinum as catalysts for the oxygen reduction reaction. The interest in this technology has increased exponentially over the recent years. Unfortunately, the low durability of anion exchange membranes (AEM) in basic conditions limits their use on a large scale. We present in this review composite AEM with one-dimensional, two-dimensional and three-dimensional fillers, an approach commonly used to enhance the fuel cell performance and stability. The most important filler types, which are discussed in this review, are carbon and titanate nanotubes, graphene and graphene oxide, layered double hydroxides, silica and zirconia nanoparticles. The functionalization of the fillers is the most important key to successful property improvement. The recent progress of mechanical properties, ionic conductivity and FC performances of composite AEM is critically reviewe
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