Search results for "Methanol"

showing 10 items of 1026 documents

Direct synthesis of dimethyl carbonate with supercritical carbon dioxide: characterization of a key organotin oxide intermediate

2006

The direct synthesis of dimethyl carbonate (DMC) using carbon dioxide as solvent and reagent for its fixation to methanol was explored with din-butyldimethoxystannane in order to get insight into the reaction mechanism for activity improvement. Catalytic runs including recycling experiments allowed isolation and characterization by NMR, IR, and single-crystal X-ray diffraction of a new tin complex containing 10 tin atoms. This compound could be prepared independently and is considered as a resting species. The yield of DMC is highest under 20 MPa pressure that fits with a monophasic supercritical medium in agreement with fluid phase equilibria calculations. In line, preliminary kinetics and…

Reaction mechanismdibutyldimethoxystannaneSupercritical carbon dioxide010405 organic chemistryInorganic chemistryorganotin oxide[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryGeneral Chemistry[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesStannaneCatalysisSupercritical fluid0104 chemical sciencesCatalysischemistry.chemical_compoundcarbon dioxide–methanol phase diagramschemistrysupercritical carbon dioxideReagentdimethyl carbonateMethanolDimethyl carbonateComputingMilieux_MISCELLANEOUS
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Double cross-linked polyetheretherketone proton exchange membrane for fuel cell

2012

Abstract The proton exchange membrane based on polyetheretherketone was prepared via two steps of cross-linking. The properties of the double cross-linked membrane (water uptake, proton conductivity, methanol permeability and thermal stability) have been investigated for fuel cell applications. The prepared membrane exhibited relatively high proton conductivity, 3.2 × 10 −2  S cm −1 at room temperature and 5.8 × 10 −2  S cm −1 at 80 °C. The second cross-linking significantly decreased the water uptake of the membrane. The performance of direct methanol fuel cell was slightly improved as compared to Nafion ® 117 due to its low methanol permeability. The results indicated that the double cros…

Renewable Energy Sustainability and the EnvironmentChemistryInorganic chemistryEnergy Engineering and Power TechnologyProton exchange membrane fuel cellElectrolyteConductivityCondensed Matter Physicschemistry.chemical_compoundDirect methanol fuel cellFuel TechnologyMembraneNafionThermal stabilityMethanolInternational Journal of Hydrogen Energy
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Methanol and proton transport through chitosan-phosphotungstic acid membranes for direct methanol fuel cell

2020

Composite chitosan-phosphotungstic acid membranes were synthesized by ionotropic gelation. Their liquid uptake is higher for thin membranes (23 ± 2 μm), while it is lower (~70%) for thicker membranes (50-70 μm). Polarization curves recorded using single module fuel cell at 70°C allowed to estimate a peak power density of 60 mW cm−2 by using 1 M as methanol and low Pt and Pt/Ru loadings (0.5 and 3 mg cm−2) at the cathode and at the anode, respectively. Electrochemical impedance spectroscopy was used to estimate the membrane conductivity and to model the electrochemical behavior of methanol electrooxidation inside the fuel cell revealing a two-step mechanism mainly responsible of overall kine…

Renewable Energy Sustainability and the EnvironmentChitosan direct methanol fuel cells methanol permeability phosphotungstic acid proton conductivityEnergy Engineering and Power TechnologyChitosanchemistry.chemical_compoundDirect methanol fuel cellFuel TechnologyMembraneSettore ING-IND/23 - Chimica Fisica ApplicataNuclear Energy and EngineeringchemistryProton transportMethanolPhosphotungstic acidNuclear chemistry
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Cross-linked PEEK-WC proton exchange membrane for fuel cell

2009

Abstract The low cost proton exchange membrane was prepared by cross-linking water soluble sulfonated-sulfinated poly(oxa- p -phenylene-3,3-phthalido- p -phenylene-oxa- p -phenylene-oxy-phenylene) (SsPEEK-WC). The prepared cross-linked membrane became insoluble in water, and exhibited high proton conductivity, 2.9 × 10 −2  S/cm at room temperature. The proton conductivity was comparable with that of Nafion ® 117 membrane (6.2 × 10 −2  S/cm). The methanol permeability of the cross-linked membrane was 1.6 × 10 −7  cm 2 /s, much lower than that of Nafion ® 117 membrane.

Renewable Energy Sustainability and the EnvironmentEnergy Engineering and Power TechnologyProton exchange membrane fuel cellConductivityCondensed Matter Physicschemistry.chemical_compoundFuel TechnologyMembranechemistryPermeability (electromagnetism)NafionHydrogen fuelPeekMethanolNuclear chemistryInternational Journal of Hydrogen Energy
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Covalent-ionically cross-linked polyetheretherketone proton exchange membrane for direct methanol fuel cell

2010

Abstract In this paper, the proton exchange membrane prepared by covalent-ionically cross-linking water soluble sulfonated–sulfinated poly(oxa- p -phenylene-3,3-phthalido- p -phenylene-oxa- p -phenylene-oxy-phenylene) (SsPEEK-WC) is reported. Compared with covalent cross-linked PEEK-WC membrane, this covalent-ionically cross-linked PEEK-WC membrane exhibits extremely reduced water uptake and methanol permeability, but just slightly sacrificed proton conductivity. The proton conductivity of the covalent-ionically cross-linked PEEK-WC membrane reaches to 2.1 × 10 −2  S cm −1 at room temperature and 4.1 × 10 −2  S cm −1 at 80 °C. The methanol permeability is 1.3 × 10 −7  cm 2  s −1 , 10 times …

Renewable Energy Sustainability and the EnvironmentInorganic chemistryEnergy Engineering and Power TechnologyProton exchange membrane fuel cellConductivitychemistry.chemical_compoundDirect methanol fuel cellMembranechemistryCovalent bondPermeability (electromagnetism)NafionMethanolElectrical and Electronic EngineeringPhysical and Theoretical ChemistryNuclear chemistryJournal of Power Sources
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CCDC 291811: Experimental Crystal Structure Determination

2006

Related Article: F.A.Cotton, C.A.Murillo, S.-E.Stiriba, Xiaoping Wang, Rongmin Yu|2005|Inorg.Chem.|44|8223|doi:10.1021/ic051282c

SSS-tris(mu4-benzene-14-dicarboxylato)-hexakis(mu2-2-(diphenylphosphino)phenyl)-hexapyridyl-hexa-rhodium dichloromethane methanol sesquihydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 291816: Experimental Crystal Structure Determination

2006

Related Article: F.A.Cotton, C.A.Murillo, S.-E.Stiriba, Xiaoping Wang, Rongmin Yu|2005|Inorg.Chem.|44|8223|doi:10.1021/ic051282c

SSS-tris(mu~4~-benzene-14-dicarboxylato)-hexakis(mu~2~-2-(diphenylphosphino)phenyl)-tris(methanol)-tripyridyl-hexa-rhodium dichloromethane methanol solvate hydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Isolation of Four New CoII/CoIII and NiII Complexes with a Pentadentate Schiff Base Ligand: Syntheses, Structural Descriptions and Magnetic Studies

2011

In this paper we report the temperature and pH dependent syntheses and systematic characterization of four new Co(II)/Co(III) and Ni(II) complexes with a pentadentate Schiff base ligand H(3)L obtained by condensing 1,3,-diaminopropan-2-ol with 2-hydroxyacetophenone in 1:2 molar ratio. The room temperature syntheses involving Co(II) and Ni(II) nitrates and the ligand H(3)L lead to the isolation of the dinuclear species [Co(2)L(2)(H(2)O)] (1), and the mononuclear complex [Ni(LH)] (3), respectively, whereas refluxing at basic pH leads to the tetranuclear complexes, [Co(II)(2)Co(III)(2)L(2)(μ(3)-OMe)(2)(NO(3))(H(2)O)(2)]NO(3)·2(H(2)O) (2), and [Ni(4)L(2)(μ(3)-OMe)(2)(H(2)O)(2)]·2H(2)O (4). 1 is…

Schiff BaseSchiff baseLigandChemistryStereochemistryCoII/CoIII ComplexPh dependentMagnetic susceptibilityNiII ComplexInorganic ChemistrySolventCrystallographychemistry.chemical_compoundFerromagnetismcrystal StructureMolar ratioCoII/CoIII Complex; NiII Complex; crystal Structure; Schiff BaseMethanol
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ESR, ENDOR and TRIPLE resonance studies on radical reactions of 1,4-benzoquinone and 1,4-hydroquinone in alkaline methanol and liquid ammonia

1990

The relative signs and absolute values of the hyperfine coupling constants of different methoxy-1,4-benzoquinones were measured by ESR, ENDOR and TRIPLE resonance spectroscopy. Reactions of 1,4-benzoquinone and 1,4-hydroquinone with methanol took place in alkaline methanol, giving rise to methoxy-substituted 1,4-benzoquinones. The same substitution reaction occurred in a mixture of ammonia and methanol. The reactions depended on temperature and the alkali concentration. Coupling constants were assigned by the modified additivity relationship method. An extremely small line width of 0.014 G was measured in the ESR spectrum of deuterated 2,5-dimethoxy-1,4-benzoquinone.

SemiquinoneHydroquinoneStereochemistryRadicalInorganic chemistryGeneral ChemistryAlkali metallaw.invention14-Benzoquinonechemistry.chemical_compoundchemistrylawKinetic isotope effectGeneral Materials ScienceMethanolElectron paramagnetic resonanceMagnetic Resonance in Chemistry
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Boosting DMFC power output by adding sulfuric acid as a supporting electrolyte: Effect on cell performance equipped with platinum and platinum group …

2023

Direct methanol fuel cells (DMFCs) are promising electrochemical systems capable of producing electricity from the electrochemical oxidation of methanol and the reduction of oxygen. In this work, the effectiveness of the addition of sulfuric acid as a supporting electrolyte for methanol fuel composition was assessed. The results showed that the peak of power curve in DMFCs with Pt/C cathode electrocatalysts increased progressively from 70 mW cm−2 (0 mM of H2SO4) to 115 mW cm−2 with a concentration of 100 mM of H2SO4. These results underlined the positive effect of the addition of a supporting electrolyte in the methanol aqueous solution on the electrochemical output that was enhanced. Plati…

Settore ING-IND/23 - Chimica Fisica ApplicataRenewable Energy Sustainability and the EnvironmentMethanolElectrocatalysiFuel cellEnergy Engineering and Power TechnologySupporting electrolyteElectrical and Electronic EngineeringPhysical and Theoretical ChemistryOxygen reduction reaction
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