Search results for "ACID"

showing 10 items of 13107 documents

Oxidative Dehydrogenation of Ethanol on Gold : Combination of Kinetic Experiments and Computation Approach to Unravel the Reaction Mechanism

2021

Abstract Selective alcohol dehydrogenation on heterogeneous catalysts is a key industrial reaction for production of aldehydes, ketones, and carboxylic compounds. Design of catalysts with improved activity and selectivity requires understanding of the reaction mechanism and kinetics. Herein, experiments, density functional theory (DFT) and kinetic modelling were combined to elucidate the mechanism and kinetics of ethanol oxidative dehydrogenation to acetaldehyde on gold catalysts. Catalytic experiments clearly emphasized the role of oxygen in this reaction. Ethanol conversion was rather independent on the gold cluster size. Formation of minor products, acetic acid and ethyl acetate was stru…

inorganic chemicalsReaction mechanismetanoliethanol oxidationEthyl acetatemechanismAlcohol010402 general chemistryHydrogen atom abstractionreaktiomekanismit01 natural sciences7. Clean energyDFTCatalysiskultaCatalysischemistry.chemical_compoundAcetic acidComputational chemistryDehydrogenationPhysical and Theoretical Chemistryasetaldehydikemialliset reaktiot010405 organic chemistryAcetaldehydegold0104 chemical scienceschemistrykineticskatalyysi
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Capsaicin desensitization in vivo is inhibited by ruthenium red.

1990

The effect of systemic administration of Ruthenium Red on the excitatory and desensitizing effect of capsaicin was investigated in rats. Ruthenium Red was injected s.c. 30 min before capsaicin was administered. The excitatory effect of capsaicin on corneal, perivascular and visceral afferents was not influenced by treatment with Ruthenium Red. However, determination of the neuropeptide content and evoked neuropeptide release in peripheral organs and dorsal spinal cord 48 h after treatment showed that Ruthenium Red attenuated the 'desensitizing' effect of capsaicin at peripheral, but not at central, endings of primary afferents. On the other hand, a capsaicin-elicited autonomic reflex mediat…

inorganic chemicalsRuthenium redCalcitonin Gene-Related PeptideInjections SubcutaneousCentral nervous systemUrinary BladderNeuropeptideBlood PressurePharmacologySubstance PSynaptic Transmissionchemistry.chemical_compoundIn vivootorhinolaryngologic diseasesAutonomic reflexmedicineAnimalsNeurons AfferentPharmacologyNerve EndingsNeuronsChemistryNeuropeptidesRats Inbred StrainsRuthenium RedRatsmedicine.anatomical_structureCapsaicinAnesthesiaExcitatory postsynaptic potentiallipids (amino acids peptides and proteins)NeuronCapsaicinEuropean journal of pharmacology
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The measurement of impurities in silicon for solar cell production

2012

The power conversion efficiency of solar cells is largely dependent on impurity levels in silicon. In the current investigations two sample preparation methods of silicon had been used before analysis - acid dissolution at atmospheric pressure and pressured microwave assisted technique. Quantification of impurities in solar silicon was done by inductively coupled plasma mass spectrometry and electrothermal atomic spectrometry. Microwave assisted dissolution of solar silicon was more effective compared to the traditional dissolution method on the hot plate, but complete dissolution of impurities and silicon matrix was achieved with a nitric and hydrofluoric acid mixture. The mass of solar si…

inorganic chemicalsSiliconPhysics::Instrumentation and DetectorsChemistrytechnology industry and agricultureAnalytical chemistrychemistry.chemical_elementAtomic spectroscopyequipment and suppliescomplex mixtureslaw.inventionstomatognathic diseaseschemistry.chemical_compoundHydrofluoric acidlawImpuritySolar cellDissolutionInductively coupled plasma mass spectrometryMicrowaveIOP Conference Series: Materials Science and Engineering
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Receptor-mediated uptake of boron-rich neuropeptide y analogues for boron neutron capture therapy.

2014

Peptidic ligands selectively targeting distinct G protein-coupled receptors that are highly expressed in tumor tissue represent a promising approach in drug delivery. Receptor-preferring analogues of neuropeptide Y (NPY) bind and activate the human Y1 receptor subtype (hY1 receptor), which is found in 90% of breast cancer tissue and in all breast-cancer-derived metastases. Herein, novel highly boron-loaded Y1 -receptor-preferring peptide analogues are described as smart shuttle systems for carbaboranes as (10) B-containing moieties. Various positions in the peptide were screened for their susceptibility to carbaborane modification, and the most promising positions were chosen to create a mu…

inorganic chemicalsStereochemistrymedia_common.quotation_subjectMolecular Sequence Datachemistry.chemical_elementPeptideBoron Neutron Capture TherapyBreast NeoplasmsBiochemistrySolid-phase synthesisDrug DiscoveryChlorocebus aethiopsAnimalsHumansNeuropeptide YAmino Acid SequenceGeneral Pharmacology Toxicology and PharmaceuticsReceptorInternalizationBoronBoranesmedia_commonPharmacologychemistry.chemical_classificationChemistryOrganic ChemistryReceptor-mediated endocytosisNeuropeptide Y receptorReceptors Neuropeptide YHEK293 CellsDrug deliveryCOS CellsMolecular MedicineFemaleChemMedChem
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Electronic and Steric Effects: How Do They Work in Ionic Liquids? The Case of Benzoic Acid Dissociation

2010

The need to have a measure of the strength of some substituted benzoic acids in ionic liquid solution led us to use the protonation equilibrium of sodium p-nitrophenolate as a probe reaction, which was studied by means of spectrophotometric titration at 298 K. In order to evaluate the importance of electronic effect of the substituents present on the aromatic ring, both electron-withdrawing and -donor substituents were taken into account. Furthermore, to have a measure of the importance of the steric effect of the substituents both para- and ortho-substituted benzoic acids were analyzed. The probe reaction was studied in two ionic liquids differing for the ability of the cation to give hydr…

inorganic chemicalsSteric effectsionic liquids ion pair formation carboxylic acidsChemistryHydrogen bondorganic chemicalsOrganic ChemistryInorganic chemistryProtonationSettore CHIM/06 - Chimica OrganicaDissociation (chemistry)chemistry.chemical_compoundIonic liquidElectronic effectEquilibrium constantBenzoic acidThe Journal of Organic Chemistry
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Sorption of uranium(VI) onto ferric oxides in sulfate-rich acid waters.

2003

The mechanisms of the uranium(VI) sorption on schwertmannite and goethite in acid sulfate-rich solutions were studied by Extended X-ray Absorption Fine Structure (EXAFS) spectroscopy. The samples were prepared under N2 atmosphere and initial uranium(VI) concentrations of 1 x 10(-5) (pH 6.5) to 5 x 10(-5) M (pH 4.2). The ionic strength was adjusted using 0.01 M Na2SO4 or 0.01 M NaClO4, respectively. The EXAFS structural parameters for uranium(VI) sorbed on goethite in sulfate-rich, acid and near-neutral solutions indicate that uranium(VI) forms an inner-sphere, mononuclear, bidentate surface complex. This complex is characterized by a uranium-ferric-iron distance of approximately 3.45 A. Ura…

inorganic chemicalsWater Pollutants RadioactiveGoethiteschwertmanniteInorganic chemistrychemistry.chemical_elementcomplex mixturesFerric Compoundsuraniumchemistry.chemical_compoundPerchlorateAdsorptionmedicinegoethiteEnvironmental ChemistrySulfatesorptionSulfatesSchwertmannitetechnology industry and agricultureSorptionGeneral ChemistryUraniumEXAFSchemistryvisual_artvisual_art.visual_art_mediumFerricUraniumAdsorptionacid mine drainagemedicine.drugEnvironmental MonitoringEnvironmental sciencetechnology
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Determination of the Absolute Density of Fe3+ and Ni2+ Ions in Langmuir-Blodgett Films

1996

By means of the Langmuir–Blodgett (LB) technique, mono- and multilayers of Ni2+ and Fe3+ containing fatty acid salts are transferred onto silicon wafers. After thermal treatment, oxidic layers can be produced. The absolute amounts of Fe3+ and Ni2+ ions per monolayer of LB film were measured and calculated by three different methods. In the case of nickel, the amount expected from theory and preparation conditions was obtained experimentally. In contrast, about twice the number of Fe3+ ions as expected is transferred. An explanation can be given by the presence of hydroxide groups bound to iron. The mean film thickness of the oxidic layers after thermal treatment was estimated where the thic…

inorganic chemicalsX-rayAnalytical chemistrychemistry.chemical_elementSurfaces and InterfacesGeneral ChemistryThermal treatmentCondensed Matter PhysicsLangmuir–Blodgett filmSurfaces Coatings and FilmsIonchemistry.chemical_compoundNickelchemistryMonolayerMaterials ChemistryHydroxideStearic acidSurface and Interface Analysis
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Predicting the activity of single isolated Lewis acid sites in solid catalysts.

2006

An experimental study of the activity of Ti-, Zr- and Sn-beta catalysts in different types of oxidation reactions is combined with a quantum-chemical analysis of the electronic properties of the active sites and the adsorbed reactants. The differences observed in the catalytic behaviour of the three materials are explained in terms of the molecular orbital distribution of each system. The intrinsic Lewis acid strength of the isolated active site, the degree of back-donation from the catalyst to the empty orbitals of the organic reactant and the net atomic charges on selected atoms are proposed as predictors of reactivity.

inorganic chemicalsbiologyChemistryOrganic ChemistryInorganic chemistryActive siteGeneral ChemistryRedoxCatalysisCatalysisAdsorptionAtomic orbitalbiology.proteinMolecular orbitalReactivity (chemistry)Lewis acids and basesChemistry (Weinheim an der Bergstrasse, Germany)
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An unexpected ring carboxylation in the electrocarboxylation of aromatic ketones

2006

The electrocarboxylation of various aromatic ketones, carried out in N-methyl-2-pyrrolidone (NMP) in a diaphragmless cell equipped with a carbon cathode and an aluminium sacrificial anode, yielded, among the products, the target hydroxy acids, the corresponding alcohols and pinacols and, quite surprisingly, detectable amounts of substituted benzoic acids and cycloexene carboxylic acids. These compounds arise from a never reported before electrocarboxylation on the aromatic ring, respectively, for substitution of an aromatic hydrogen and from an addition reaction. For example, the electrocarboxylation of acetophenone gave rise to the substituted benzoic acids in ortho, para and meta position…

inorganic chemicalschemistry.chemical_classificationAddition reactionKetoneorganic chemicalsGeneral Chemical EngineeringReaction intermediateSettore ING-IND/27 - Chimica Industriale E TecnologicaHydrogen atom abstractionchemistry.chemical_compoundMeta-chemistryCarboxylationElectrochemistryOrganic chemistryElectrocarboxylationRing carboxylationKetonesCarbon dioxideUndivided cellsBenzoic acidAcetophenone
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A kinetic study of the basic hydrolysis of 2-phenylethyl nitrite in the presence of borate buffer and β-cyclodextrin

2002

The kinetics of the hydrolysis of 2-phenylethyl nitrite have been studied in basic aqueous solutions (borate buffer) in the absence and presence of β-cyclodextrin. The observed kinetic trends show that the hydrolysis reaction consists of at least three subsequent processes. The first is a fast acid-base reaction between the boron atom of boric acid and oxygen atom of the alkyl nitrite. The second one should be the nucleophilic attack of hydroxyl ion on the alkyl nitrite. The last process could be referred to as a combination of transfer of hydrogen acid to a water molecule followed by ruptures of nitrogen-oxygen and boron-oxygen bonds. The effect of β- cyclodextrin on each process is also d…

inorganic chemicalschemistry.chemical_classificationAqueous solutionCyclodextrinOrganic ChemistryKineticsInorganic chemistryMedicinal chemistrylcsh:QD241-441Boric acidchemistry.chemical_compoundHydrolysislcsh:Organic chemistryNucleophilechemistryNitriteAlkylArkivoc
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