Search results for "oxalic acid."

showing 10 items of 59 documents

Inhibitoren der Korrosion 22 (1) - Einfluß von pH, Sauerstoff, Fremdionen, Art und Konzentration von Säuren auf den Korrosionsverlauf von Aluminium

1978

Die Korrosion von Aluminium unter Sauerstoff verlauft praktisch unabhangig vom pH-Wert, und zwar sowohl unter Sauerstoffverbrauch als auch unter Wasserstoffentwicklung. Dieses Verhalten wird sowohl in einer Acetatpuffer/Natriumchloridlosung als auch in anorganischen (Salpeter-, Schwefel-Phosphor- und Salzsaure) als auch in organischen Sauren gefunden. Bei den organischen Sauren sind die Ergebnisse jedoch nicht so eindeutig; in Essigsaure wird die Korrosionsgeschwindigkeit durch Natriumchloridzusatz nicht beeinflust, ebenso in Ameisensaure, wahrend Oxalsaure nur bei Anwesenheit von Natriumchlorid Wasserstoff entwickelt. Zitronensaure bewirkt uberhaupt keine Wasserstoffentwicklung. Als am bes…

Formic acidMechanical EngineeringSodiumOxalic acidMetals and Alloyschemistry.chemical_elementHydrochloric acidGeneral MedicineOxygenSurfaces Coatings and Filmschemistry.chemical_compoundAcetic acidchemistryMechanics of MaterialsAluminiumMaterials ChemistryEnvironmental ChemistryCitric acidNuclear chemistryMaterials and Corrosion
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Retention-pH profiles of acids and bases in hydrophilic interaction liquid chromatography

2018

Abstract The high proportion of acetonitrile used in many HILIC mobile phases significantly changes the acid-base properties of pH buffers and analytes foreseen from available data in water. In this paper, the recommended stability pH range for chromatographic columns is examined with various acetonitrile/water mixtures, resulting in a significant broadening in the operational pH window with the content of organic solvent. Additionally, the challenge of buffer selection in HILIC is also addressed. Commonly used ammonium acetate shrinks its pH buffering range in acetonitrile-rich mobile phases due to variations in the dissociation constants of the buffer constituents (acetic acid and ammoniu…

Formic acidOxalic acidHydrogen-ion concentrationLiquid chromatography02 engineering and technology01 natural sciencesBiochemistryCromatografia de líquidsAnalytical Chemistrychemistry.chemical_compoundAcetic acidSuccinimideEquilibri àcid-baseConcentració dels ions d'hidrogenEnvironmental ChemistryAcetonitrileTriethylamineSpectroscopyChromatographyHydrophilic interaction chromatography010401 analytical chemistry021001 nanoscience & nanotechnology0104 chemical sciencesAcid-base equilibriumchemistry0210 nano-technologyAmmonium acetate
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Photolysis of HCOOH monomer and dimer in solid argon: Raman characterization of in situ formed molecular complexes

2010

Raman spectroscopy combined with the matrix isolation technique was employed to study the 193-nm photodecomposition products of formic acid in an argon matrix. The Raman-active fundamentals belonging to the CO(2) + H(2) and CO + H(2)O photoproducts were assigned. Also, bands due to Fermi resonance between the stretching vibration (nu(1)) and the overtone of the bending mode (2nu(2)) of CO(2) were identified. Both ortho- and para-H(2) molecules were identified from their rotational lines S(0)(1) and S(0)(0), respectively. These bands appeared upon matrix annealing as well as after prolonged photolysis. Additionally, photolysis of FA dimers produces oxalic acid and its secondary photoproducts…

Formic acidStereochemistryDimerOxalic acidPhotodissociationMatrix isolationGeneral Physics and AstronomyPhotochemistrychemistry.chemical_compoundsymbols.namesakechemistryAb initio quantum chemistry methodssymbolsFermi resonancePhysical and Theoretical ChemistryRaman spectroscopyPhysical Chemistry Chemical Physics
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The Preparation and Characterization of New Antazoline Salts with Dicarboxylic Acids

2015

New antazoline salts with organic acids (fumaric acid, oxalic acid, and maleic acid) were prepared. The effect of the crystallization solvent and mechanochemical treatment on the crystalline forms of these salts was studied. Two polymorphs of antazoline hydrogen maleate were identified and their relative stability was determined. The molecular structures of antazoline hydrogen oxalate and antazoline hydrogen maleate showed differences in antazoline cation conformation. In crystal structures of all salts both imidazoline nitrogens of antazoline cation are involved in hydrogen bond formation with carboxyl groups of the acid.

Fumaric acidMaleic acidHydrogen bondOxalic acidGeneral ChemistryCondensed Matter PhysicsOxalateSolventchemistry.chemical_compoundchemistryPolymorphism (materials science)Polymer chemistryAntazolinemedicineOrganic chemistryGeneral Materials Sciencemedicine.drugMolecular Crystals and Liquid Crystals
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Anodic abatement of organic pollutants in water in micro reactors

2010

The electrochemical oxidation of oxalic acid (OA) was performed in a micro flow cell equipped with a boron doped diamond (BDD) anode. This preliminary study demonstrates that a flow cell with a micrometric distance between the cathode and the anode can be used to perform the electrochemical treatment of waters contaminated by organic pollutants in the absence of added supporting electrolytes with high abatements. The effect of the distance between the cathode and the anode, the flow rate and the current density on the abatement of oxalic acid and on the current efficiency was in particular studied.

General Chemical EngineeringOxalic acidInorganic chemistrychemistry.chemical_element02 engineering and technologyElectrolyteWastewater treatment010402 general chemistryElectrochemistry01 natural sciencesAnalytical Chemistrylaw.inventionchemistry.chemical_compoundlaw[CHIM.ANAL]Chemical Sciences/Analytical chemistryElectrochemistryMicro deviceBoronMicro reactorComputingMilieux_MISCELLANEOUSElectrochemical abatementSettore ING-IND/27 - Chimica Industriale E Tecnologica021001 nanoscience & nanotechnologyOxidation of organic6. Clean waterCathode0104 chemical sciencesAnode[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry13. Climate actionElectrodeMicroreactor0210 nano-technologyBDD
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Electrochemical treatment of aqueous solutions containing one or many organic pollutants at boron doped diamond anodes. Theoretical modeling and expe…

2012

The electrochemical oxidation of organics in water at boron doped diamonds (BDD) was experimentally investigated with the aim to discuss the correlations among the conversion of the pollutants and the instantaneous current efficiency ICE with the operative conditions. A simple theoretical model previously developed for the oxidation of oxalic acid accounting for the cases of mass transfer control, oxidation reaction control and mixed kinetic regimes was adopted and extended to challenge its predictive capability in the case of organics of different nature and in systems with more pollutants. A quite good agreement, between theoretical predictions and experimental data pertaining to the elec…

General Chemical EngineeringRadicalChlorine compoundOxalic acidInorganic chemistryPollution Anodic oxidationElectrochemistryCarboxylic acidRedoxIndustrial and Manufacturing Engineeringchemistry.chemical_compoundElectron transferAOPs; BDD; Diamond anode; Oxygen evolution; Theoretical models Boron; Carboxylic acids; Chlorine compounds; Diamonds; Electrochemical oxidation; Electron transitions; Free radical reactions; Pollution Anodic oxidationMass transferDiamond anodeEnvironmental ChemistryAOPElectron transitionAqueous solutionOxygen evolutionGeneral ChemistrySettore ING-IND/27 - Chimica Industriale E TecnologicaFree radical reactionTheoretical models BoronElectrochemical oxidationchemistryDiamondBDDOxygen evolutionChemical Engineering Journal
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Bio-based 1,3-diisobutyl imidazolium hydrogen oxalate [iBu 2 IM](HC 2 O 4 ) as CO 2 shuttle

2017

International audience; This manuscript describes the using of biosourced L-valine, oxalic acid and glyoxal to produce a biobased imidazolium hydrogen oxalate [iBu(2)IM](HC2O4) which is converted to its related hydrogen carbonate salt by a simple electrolysis without using strong base. The addition of weak protic acids to the latter compound leads to a rapid and quantitative CO2 release with formation of the starting hydrogen oxalate salt or a new halide free bio-based ionic liquid [iBu(2)IM](AcO) which is able to adsorb reversibly the CO2 at room temperature. The protonation reactions, combined with electrolysis, could then be a promising alternative solution for storage and transport of C…

HydrogenOxalic acidInorganic chemistryHalideSalt (chemistry)chemistry.chemical_elementProtonation010402 general chemistrycarbon-dioxide01 natural sciences[ CHIM ] Chemical SciencesOxalatelaw.inventionefficientionic liquidschemistry.chemical_compoundlawstabilized phosphenium adductsEnvironmental Chemistry[CHIM]Chemical Scienceselectrochemical reductioncaptureacidsmethanolchemistry.chemical_classificationElectrolysis010405 organic chemistrycrystal-structurePollution0104 chemical scienceschemistrydimethyl-sulfoxideIonic liquid
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Characterization of a new, nonpathogenic mutant of Botrytis cinerea with impaired plant colonization capacity.

2006

International audience; Botrytis cinerea is a necrotrophic pathogen that attacks more than 200 plant species.Here, the nonpathogenic mutant A336, obtained via insertional mutagenesis, was characterized.Mutant A336 was nonpathogenic on leaves and fruits, on intact and wounded tissue, while still able to penetrate the host plant. It grew normally in vitro on rich media but its conidiation pattern was altered. The mutant did not produce oxalic acid and exhibited a modified regulation of the production of some secreted proteins (acid protease 1 and endopolygalacturonase 1). Culture filtrates of the mutant triggered an important oxidative burst in grapevine ( Vitis vinifera ) suspension cells, a…

Hypersensitive responsehypersensitive responsePhysiology[SDV]Life Sciences [q-bio]colonisationMutantArabidopsisConidiationPlant ScienceMicrobiologyInsertional mutagenesisFungal Proteins03 medical and health sciencesPlasmidGene Expression Regulation FungalOnionsBotrytis cinerea; endopolygalacturonase BcPG1; hypersensitive responseVitismutantoxidative burstPathogenGene030304 developmental biologyBotrytis cinereaPhaseolus0303 health sciencesoxalateendopolygalacturonase BcPG1biology030306 microbiologyOxalic Acidfungifood and beveragesHydrogen-Ion Concentrationbiology.organism_classificationImmunity Innatenonpathogenic mutantEnzymesPlant LeavesMutagenesis Insertionalnonaspartyl acid protease ACP1Mutationbotrytis cinerea;endopolygalacturonase BcPG1;hypersensitive response;nonaspartyl acid protease ACP1;nonpathogenic mutant;oxalate;oxidative burstBotrytisbotrytis cinereaReactive Oxygen SpeciesThe New phytologist
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Chiral Organometallic Triangles with Rh−Rh Bonds. 2. Compounds Prepared from Enantiopure cis-Rh2(C6H4PPh2)2(OAc)2(HOAc)2 and Their Catalytic Potentia…

2005

Enantiomers of the orthometalated dirhodium compound cis-Rh2(C6H4PPh2)2(OAc)2(HOAc)2 (R-1 and S-1) were prepared from carboxylate exchange reactions of the resolved diasteroisomers of cis-Rh2(C6H4PPh2)2(protos)2(H2O)2 (protos = N-4-methylphenylsulfonyl-l-proline anion) and acetic acid. These compounds react with excess Me3OBF4 in CH3CN, producing the enantiomers of [cis-Rh2(C6H4PPh2)2(CH3CN)6](BF4)2 (R-2 and S-2) which have six labile and replaceable CH3CN ligands in equatorial and axial positions. Reactions of R-2 and S-2 with tetraethylammonium salts of the linear dicarboxylic acids, terephthalic acid (HO2CC6H4CO2H), oxalic acid (HO2CCO2H), and 4,4'-diphenyl-dicarboxylic acid (HO2CC6H4C6H…

Inorganic ChemistryTerephthalic acidAcetic acidchemistry.chemical_compoundEnantiopure drugchemistryStereochemistryOxalic acidCarboxylatePhysical and Theoretical ChemistryEnantiomerMedicinal chemistryCatalysisInorganic Chemistry
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Role of Deprotonation and Cu Adatom Migration in Determining the Reaction Pathways of Oxalic Acid Adsorption on Cu(111)

2011

Scanning tunneling microscopy (STM), X-ray photoelectron spectroscopy (XPS), and first principles theoretical calculations have been used to gain insight into the fundamental processes involved in the adsorption and self-assembly of oxalic acid on Cu(111). The experimental data demonstrate that several reaction pathways are involved in the chemisorption of oxalic acid on Cu(111), one of which leads to deprotonation of the acid into oxalate molecules that form ordered structures on the surface. Theoretical calculations indicate that the adsorption of oxalate molecules is not stable on the surface unless copper adatoms are taken into consideration. Coordination with copper adatoms prevents ox…

Inorganic chemistryOxalic acidPhotochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionchemistry.chemical_compoundGeneral EnergyAdsorptionDeprotonationchemistryX-ray photoelectron spectroscopylawPhysical and Theoretical ChemistryScanning tunneling microscopeThe Journal of Physical Chemistry C
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