Search results for "Kinetics"

showing 10 items of 2224 documents

Nanopore charge inversion and current-voltage curves in mixtures of asymmetric electrolytes

2018

[EN] We consider the screening of the negative charges (carboxylic acid groups) fixed on the surface of a conical-shaped track-etched nanopore by divalent magnesium (Mg2+) and trivalent lanthanum (La3+). The experimental current (I)-voltage (V) curves and current rectification ratios allow discussing fundamental questions about the overcompensation of spatially-fixed charges by multivalent ions over nanoscale volumes. The effects of charge inversion or reversal on nanopore transport are discussed in mixtures of asymmetric electrolytes (LaCl3 and MgCl2 with KCl). In particular, pore charge inversion is demonstrated for La3+ as well as for mixtures of this trivalent ion at low concentrations …

inorganic chemicalsCharged nanoporeMaterials scienceKineticschemistry.chemical_elementFiltration and Separation02 engineering and technologyElectrolyte010402 general chemistry01 natural sciencesBiochemistryDivalentIonLanthanumGeneral Materials SciencePhysical and Theoretical ChemistryMaterialsAsymmetric electrolyteschemistry.chemical_classificationCharge inversionNanotecnologiaCurrent rectification021001 nanoscience & nanotechnology0104 chemical sciencesNanoporeHysteresisMembranechemistryChemical physicsCurrent-voltage curveFISICA APLICADA0210 nano-technology
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<i>Geminal</i> Parahydrogen-Induced Polarization: Accumulating Long-Lived Singlet Order on Methylene Proton Pairs

2020

Abstract. In the majority of hydrogenative PHIP (Parahydrogen Induced Polarization) experiments, the hydrogen molecule undergoes pairwise cis-addition to an unsaturated precursor to occupy vicinal positions on the product molecule. However, some ruthenium-based hydrogenation catalysts induce geminal hydrogenation, leading to a reaction product in which the twohydrogen atoms are transferred to the same carbon center, forming a methylene (CH2) group. The singlet order of parahydrogen is substantially retained over the geminal hydrogenation reaction, giving rise to a singlet-hyperpolarized CH2 group. Although the T1 relaxation times of the methylene protons are often short, the singlet order h…

inorganic chemicalsGeminalHydrogen010405 organic chemistrychemistry.chemical_element010402 general chemistrySpin isomers of hydrogenPhotochemistry01 natural sciencesChemical reaction0104 chemical sciencesChemical kineticschemistry.chemical_compoundchemistryMoleculeSinglet stateMethylene
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The fnr Gene of Bacillus licheniformis and the Cysteine Ligands of the C-Terminal FeS Cluster

1998

Many of the O2-responsive gene regulators of bacteria are members of the fumarate nitrate reductase-cyclic AMP receptor protein family of transcriptional regulators (12, 13, 15, 17) with predicted structures similar to those of the cyclic AMP receptor protein (11). The Fnr (stands for fumarate nitrate reductase regulator) protein from Escherichia coli (FnrEc) controls the expression of a variety of genes, mainly of anaerobic respiration and metabolism (5, 13). It contains a N-terminal cluster of three essential cysteine residues which are supposed to bind together with Cys122 a [4Fe 4S]2+ cluster which is required for O2 sensing (4, 7, 8, 10, 16). A wide variety of gram-negative bacteria co…

inorganic chemicalsIron-Sulfur ProteinsMolecular Sequence DataRestriction MappingMutantBacillusGenetics and Molecular BiologySequence alignmentmacromolecular substancesBacillus subtilisLigandsNitrate reductaseenvironment and public healthMicrobiologyBacterial ProteinsAmino Acid SequenceCysteineBacillus licheniformisMolecular BiologyPeptide sequenceBacillus megateriumSequence Homology Amino AcidbiologyEscherichia coli ProteinsGene Expression Regulation Bacterialbiology.organism_classificationenzymes and coenzymes (carbohydrates)KineticsBiochemistryBacillus megateriumbacteriaSequence AlignmentBacillus subtilisTranscription FactorsCysteineJournal of Bacteriology
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The Myristoylated Alanine-Rich C-Kinase Substrate (MARCKS) is Sequentially Phosphorylated by Conventional, Novel and Atypical Isotypes of Protein Kin…

1995

The myristoylated alanine-rich C-kinase substrate (MARCKS) is the major protein kinase C (PKC) substrate in many cell types including fibroblasts and brain cells. Here we describe the phosphorylation of MARCKS and the site specificity for different PKC isotypes. Conventional (c)PKC beta 1, novel (n)PKC delta and nPKC epsilon efficiently phosphorylated the MARCKS protein in vitro. The Km values were extremely low, reflecting a high affinity between kinases and substrate. The apparent affinity of nPKC delta (Km = 0.06 microM) was higher than that of nPKC epsilon and cPKC beta 1 (Km = 0.32 microM). The rate of substrate phosphorylation was inversely correlated with affinity and decreased in th…

inorganic chemicalsKinaseChemistryIntracellular Signaling Peptides and ProteinsMembrane ProteinsProteinsContext (language use)macromolecular substancesenvironment and public healthBiochemistryMolecular biologyCell biologyIsoenzymesSerineKineticsenzymes and coenzymes (carbohydrates)Substrate-level phosphorylationbacteriaPhosphorylationPhosphorylationMARCKSMyristoylated Alanine-Rich C Kinase SubstrateProtein Kinase CProtein kinase CMyristoylationEuropean Journal of Biochemistry
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Dissociation-constants of metat-ion-complexes with alkaline phosphatase from pig kidney.

1976

Using metal-ion buffers it was possible to remove Zn2+, Mg2+ and Mn2+ ions of pig kidney alkaline phosphatase reversibly. The dissociation constants obtained are KEMg: 4 X 10(-7) M, KEMn: 4 X 10(-8) M and KEZn: 8 X 10(-13) M (22 degrees C, pH: 9.6, mu: 0.07).

inorganic chemicalsPharmacologyManganeseChemistryCations DivalentSwinePig kidneyIronInorganic chemistryCell BiologyAlkaline PhosphataseKidneyIonDissociation constantCellular and Molecular NeuroscienceKineticsZincMolecular MedicineAlkaline phosphataseAnimalsCalciumMagnesiumMolecular BiologyExperientia
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Determination of boron concentration in blood and tissue samples from patients with liver metastases of colorectal carcinoma using Prompt Gamma Ray A…

2010

As part of the studies on Boron Neutron Capture Therapy at the University of Mainz, Germany, a clinical trial has been started, in which our patients suffering from liver metastases of colorectal carcinoma, have been enrolled. Specimens of blood and healthy tissue samples taken from the patients were measured at the PGAA facilities at the HFR in Petten, The Netherlands, and at the FRM II in Munich, Germany. From the measured boron concentrations, pharmacokinetic curves and blood-to-tissue concentration ratios were produced.

inorganic chemicalsRadiationbusiness.industryColorectal cancerLiver NeoplasmsGamma raychemistry.chemical_elementHealthy tissuemedicine.diseaseBoron concentrationPharmacokineticschemistryMedicineHumansbusinessBoronNuclear medicineColorectal NeoplasmsBoronApplied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine
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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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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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Heterogeneous fenton oxidation using magnesium ferrite nanoparticles for ibuprofen removal from wastewater: optimization and kinetics studies

2020

In this study, the catalytic properties of Fenton-like catalyst based on magnesium ferrite nanoparticles for IBP degradation were examined. Structural and morphological studies showed the low crystallinity and mesoporous structure for the catalyst obtained via a glycine-nitrate method. The influences of catalyst dosage, oxidant concentration, and solution pH on the pollutant degradation were investigated. The pseudo-first-order model describes kinetic data, and under optimal condition (catalyst dose of 0.5 g L-1, H2O2 concentration of 20.0 mM, and pH of 8.0), apparent rate constant reached 0.091 min-1. It was shown that Fenton reaction was mainly induced by iron atoms on the catalyst surfac…

inorganic chemicalshapetusMaterials scienceArticle SubjectKineticsNanoparticlejätevesi02 engineering and technology010501 environmental sciences01 natural sciencesCatalysisCrystallinitykatalyytitReaction rate constantT1-995General Materials ScienceTechnology (General)jäteveden käsittely0105 earth and related environmental sciencesvedenpuhdistusmagnesium ferrite ; ibuprofen removal ; fenton oxidationlääkeaineet021001 nanoscience & nanotechnologyibuprofeeniWastewaterChemical engineeringnanohiukkasetLeaching (metallurgy)0210 nano-technologyMesoporous material
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Myocardial Glutathione Alterations in Acute Coronary Occlusion in the Dog

1987

Glutathione (GSH) decreases in dog mycocardium upon acute coronary occlusion when compared with sham-operated dogs. Total glutathione content (GSHeq = GSH + ZGSSG) remains unchanged throughout the experiment (6 h after surgery) in both sham- and acute coronary occlusion-operated dogs. GSSG and GSH/GSSG ratio increases and decreases respectively in all animals but tends to reach the normal value after 6 h in sham-operated dogs. Both parameters (GSSG and GSH/GSSG ratio) remain altered in acute coronary occlusion-operated ones. This alteration of glutathione status in ischemic myocardium is discussed.

inorganic chemicalsmedicine.medical_specialtyIschemic myocardiumIschemiaCoronary DiseaseBiochemistrychemistry.chemical_compoundDogsfluids and secretionsReference ValuesInternal medicinemedicineAnimalsNormal rangeGlutathione DisulfideTotal glutathionebusiness.industryMyocardiumGlutathionemedicine.diseaseCoronary VesselsGlutathioneKineticschemistryCoronary occlusionAnesthesiaCardiologybusinessFree Radical Research Communications
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