Search results for "Kinetic"

showing 10 items of 3064 documents

Perovskite CH3NH3PbI3–XClx Solar Cells. Experimental Study of Initial Degradation Kinetics and Fill Factor Spectral Dependence

2021

The main drawback of the methylammonium lead halide perovskite solar cells is their degradation in ambient atmosphere. To investigate ambient-air-induced cell degradation, spec-tral dependencies of open-circuit voltage (VOC), fill factor (FF) and the power conversion effi-ciency (PCE) have been acquired (for the first time reported in literature). Our custom-made measurement system allowed us to perform measurements of the above-mentioned entities in situ directly in vacuum during and after thermal deposition of the elec-trode. We also studied how these parameters in vacuum changed after cell exposure to ambient air for 85 min (50 nm top electrode) and for 180 min (100 nm top Ag electrode).…

Degradation kineticsSolid-state physicsQC1-999General Physics and AstronomyDegradation kinetics02 engineering and technology010402 general chemistry01 natural sciences7. Clean energy:NATURAL SCIENCES:Physics [Research Subject Categories]media_common.cataloged_instanceEuropean unionfill factor spectral dependencePerovskite (structure)media_commonPhysicsHorizon (archaeology)PhysicsEnergy conversion efficiencyGeneral Engineering021001 nanoscience & nanotechnologyEngineering physics0104 chemical sciencespower conversion efficiencydegradation kineticslead halide perovskitesolar cellsFill factor0210 nano-technology
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Modelling denitrification including the dynamics of denitrifiers and their progressive ability to reduce nitrous oxide: comparison with batch experim…

2005

Nitrous oxide contributes to the global greenhouse effect and affects the chemistry of O 3 in the upper troposphere and lower stratosphere. To define a relevant model for microbial NO 3 - and N 2 O reductions in soil and estimate the parameters involved, we propose a method combining measurements of anaerobic soil slurry and simulations of NO 3 - and N 2 O reductions, including non-enzymatic competition between NO 3 - and N 2 O as electron acceptors and the microbial dynamics of two denitrifier groups that are either able or unable to reduce N 2 O. Three models varying in the description of soil capability to reduce N 2 O through denitrification were assessed. The procedure was applied on a…

DenitrificationKineticsSoil ScienceMineralogyBiomass[SDV.SA.SDS]Life Sciences [q-bio]/Agricultural sciences/Soil studyBacterial growthReductaseQUALITE DES SOLS03 medical and health scienceschemistry.chemical_compound[SDV.SA.SDS] Life Sciences [q-bio]/Agricultural sciences/Soil studyComputingMilieux_MISCELLANEOUSchemistry.chemical_classification0303 health sciences030306 microbiologyChemistry04 agricultural and veterinary sciencesNitrous oxideElectron acceptorAnoxic waters6. Clean water13. Climate actionEnvironmental chemistry040103 agronomy & agriculture0401 agriculture forestry and fisheries
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Unconventional Fluorescence Quenching in Naphthalimide-Capped CdSe/ZnS Nanoparticles

2013

Core–shell (CS) CdSe/ZnS quantum dots (QD) capped with ligands that possess a mercapto or an amino group and a naphthalimide (NI) as chromophore unit, linked by a short ethylene chain (CS@S–NI and CS@H2N–NI, respectively), have been synthesized and fully characterized by infrared and nuclear magnetic resonance spectroscopies, high-resolution transmission electron microscopy, and voltammetry as well as by steady-state absorption and emission spectroscopies. The organic ligands HS–NI and H2N–NI act as bidentate ligands, thereby causing a drastic decrease in the QD emission. This was particularly evident in the case of CS@S–NI. This behavior has been compared with that of commercially availabl…

DenticityChemistryLigandKineticsNanoparticleChromophorePhotochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyTransmission electron microscopyQuantum dotPhysical and Theoretical ChemistryAbsorption (chemistry)The Journal of Physical Chemistry C
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Fast redox-triggered shuttling motions in a copper rotaxane based on a phenanthroline–terpyridine conjugate

2014

Fast shuttling motions in solution have been observed by cyclic voltammetry in a Cu(I/II)-based [2] rotaxane. In the reported system, the different coordination preferences of both copper oxidation states are exploited to promote the electrochemically-triggered gliding of the ring from a tetra to a pentacoordinated site and vice versa. The thread of this rotaxane consists of a tridentate 2,2':6',2''-terpyridine chelating unit directly bonded through its 5-position to the 3-position of the bidentate 1,10-phenanthroline unit. This distribution reduces to a minimum the distance between the two coordination sites and lessens the congestion around the tetrahedral environment. These two factors h…

DenticityRotaxaneRotaxanesPyridinesPhenanthrolineOrganic Chemistrychemistry.chemical_elementPhotochemistryElectrochemistryBiochemistryRedoxCopperKineticsMotionchemistry.chemical_compoundchemistryElectrochemistryPhysical and Theoretical ChemistryTerpyridineCyclic voltammetryOxidation-ReductionCopperPhenanthrolinesOrg. Biomol. Chem.
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DNA binding, nuclease activity, DNA photocleavage and cytotoxic properties of Cu(II) complexes of N-substituted sulfonamides.

2013

Abstract Ternary copper(II) complexes [Cu(NST)2(phen)] (1) and [Cu(NST)2(NH3)2]·H2O (2) [HNST = N-(4,5-dimethylthiazol-2-yl)naphthalene-1-sulfonamide] were prepared and characterized by physico-chemical techniques. Both 1 and 2 were structurally characterized by X-ray crystallography. The crystal structures show the presence of a distorted square planar CuN4 geometry in which the deprotonated sulfonamide, acting as monodentate ligand, binds to the metal ion through the thiazole N atom. Both complexes present intermolecular π–π stacking interactions between phenanthroline rings (compound 1) and between naphthalene rings (compound 2). The interaction of the complexes with CT DNA was studied b…

DenticityStereochemistryCell SurvivalUltraviolet RaysPhenanthrolineRadicalStackingAscorbic AcidNaphthalenesBiochemistryFluorescence spectroscopyInorganic Chemistrychemistry.chemical_compoundInhibitory Concentration 50Coordination ComplexesCell Line TumorAnimalsHumansDNA CleavageThiazoleNucleaseSulfonamidesBinding SitesbiologyCytotoxinsHydroxyl RadicalDNAHydrogen PeroxidePhotochemical ProcessesKineticschemistrybiology.proteinCattleDNACopperPhenanthrolinesJournal of inorganic biochemistry
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From the covalent linkage of drugs to novel inhibitors of ribonucleotide reductase: synthesis and biological evaluation of valproic esters of 3'-C-me…

2014

We synthesized a series of serum-stable covalently linked drugs derived from 3'-C-methyladenosine (3'-Me-Ado) and valproic acid (VPA), which are ribonucleotide reductase (RR) and histone deacetylase (HDAC) inhibitors, respectively. While the combination of free VPA and 3'-Me-Ado resulted in a clear synergistic apoptotic effect, the conjugates had lost their HDAC inhibitory effect as well as the corresponding apoptotic activity. Two of the analogs, 2',5'-bis-O-valproyl-3'-C-methyladenosine (A160) and 5'-O-valproyl-3'-C-methyladenosine (A167), showed promising cytotoxic activities against human hematological and solid cancer cell lines. A167 was less potent than A160 but had interesting featu…

Deoxyribonucleoside triphosphateAdenosineCell SurvivalClinical BiochemistryAllosteric regulationPharmaceutical ScienceAntineoplastic AgentsPharmacologyBiochemistryHistone deacetylase (HDAC) inhibitorHistone DeacetylasesAdenosine TriphosphateAllosteric RegulationCell Line TumorDrug DiscoveryRibonucleotide ReductasesmedicineValproic acidHumansRibonucleotide reductase (RR) inhibitorEnzyme InhibitorsMolecular Biology3′-C-methyladenosineNucleoside analogueKinaseChemistryOrganic ChemistryApoptosiEstersSettore CHIM/08 - Chimica FarmaceuticaHematological and solid tumorHistone Deacetylase InhibitorsKineticsRibonucleotide reductaseBiochemistrySettore BIO/14 - FarmacologiaMolecular MedicineHistone deacetylaseNucleosideIntracellularmedicine.drug
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Deoxysarpagine Hydroxylase — A Novel Enzyme Closing a Short Side Pathway of Alkaloid Biosynthesis in Rauvolfia

2002

Microsomal preparations from cell suspension cultures of the Indian plant Rauvolfia serpentina catalyze the hydroxylation of deoxysarpagine under formation of sarpagine. The newly discovered enzyme is dependent on NADPH and oxygen. It can be inhibited by typical cytochrome P450 inhibitors such as cytochrome c, ketoconazole, metyrapone, tetcyclacis and carbon monoxide. The CO-effect is reversible with light (450 nm). The data indicate that deoxysarpagine hydroxylase is a novel cytochrome P450-dependent monooxygenase. A pH optimum of 8.0 and a temperature optimum of 35 degrees C were determined. K(m) values were 25 microM for NADPH and 7.4 microM for deoxysarpagine. Deoxysarpagine hydroxylase…

Deoxysarpagine hydroxylase activityLightCytochromeStereochemistryClinical BiochemistryPharmaceutical ScienceBiochemistryRauwolfiaIndole AlkaloidsHydroxylationchemistry.chemical_compoundCytochrome P-450 Enzyme SystemRauvolfia serpentinaDrug DiscoveryMolecular BiologyPlant Proteinschemistry.chemical_classificationCarbon MonoxidebiologyChemistryDeoxysarpagine hydroxylaseCytochrome cOrganic ChemistryTemperatureHydrogen-Ion ConcentrationMonooxygenasebiology.organism_classificationSecologanin Tryptamine AlkaloidsKineticsEnzymeBiochemistrybiology.proteinMolecular MedicineAryl Hydrocarbon HydroxylasesNADPBioorganic & Medicinal Chemistry
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Determination of phenolic antioxidants in vegetal and animal fats without previous extraction by dilution with n-propanol and micellar liquid chromat…

1999

Abstract A simple and rapid HPLC method for the determination of phenolic antioxidants (propyl and octyl gallates, tert -butylhydroquinone and 3- tert -butyl-4-hydroxyanisole) in sunflower, corn and olive oils, margarine, lard and butter oil is described. The samples are diluted with n -propanol, filtered and injected; solutions containing 30% (w/w) sample can be injected. The analytes are separated with a C18 column and a micellar mobile phase containing 0.1 M SDS, 2.5% n -propanol and 10 mM phosphate of pH 3, and detected at 290 nm. Calibration curves are linear ( r  > 0.9999) and the limits of detection range from 0.2 to 1.3 ng, which correspond to antioxidant concentrations well below t…

Detection limitAnimal fatChromatographyExtraction (chemistry)BiochemistryHigh-performance liquid chromatographyMicellar electrokinetic chromatographyAnalytical ChemistryPropanolchemistry.chemical_compoundchemistryMicellar liquid chromatographyEnvironmental ChemistryPhenolsSpectroscopyAnalytica Chimica Acta
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Determination of thyreostatics in animal feed by micellar electrokinetic chromatography

1999

The determination of the thyreostatics 2-thiouracil, its derivatives (4-methyl-2-thiouracil, 4-propyl-2-thiouracil and 4-phenyl-2-thiouracil) and methimazole in manufactured dried animal feed by micellar electrokinetic chromatography (MEKC) is described. A 99 +/- 5% extraction yield at the 20 micrograms g-1 level (n = 8) was achieved by shaking the milled fodder with methanol-1 M NaOH (80 + 20). Aliquots of the supernatant were injected in a 75 microns x 33.5 cm uncoated silica capillary using pressure; separation was performed at 23 degrees C with 15 kV (positive polarity) in a background electrolyte (BGE) containing 40 mM sodium dihydrogenphosphate, 50 mM sodium dodecyl sulfate and 15 mM …

Detection limitChromatographyAnimal feedSodiumExtraction (chemistry)chemistry.chemical_elementAnimal FeedBiochemistryThiouracilMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundAntithyroid AgentschemistryFodderElectrochemistryAnimalsEnvironmental ChemistrySodium dodecyl sulfateQuantitative analysis (chemistry)SpectroscopyChromatography Micellar Electrokinetic CapillaryThe Analyst
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Determination of Parabens in Cosmetics without Previous Extraction by Micellar Liquid Chromatography

1999

A simple and rapid micellar liquid chromatography method for the determination of p-hydroxybenzoic acid esters (methyl-, ethyl-, n-propyl-, and n-butylparaben) in cosmetics (bath foam, milk lotion, hand cream, cream base, and shampoo) is described. The samples are solved with n-propanol, further diluted with more n-propanol or with an aqueous sodium dodecyl sulphate (SDS) micellar solution, and injected. Separations are performed with a micellar mobile phase containing 0.1M SDS, 2.5% n-propanol, 10mM phosphate (pH 3), and with an octadecyl silica column (C 18 ). Calibrations are linear (correlation coefficient r > 0.999) and the limits of detection range from 0.03 to 0.3 ng paraben. The det…

Detection limitChromatographyAqueous solutionintegumentary systemChemistryExtraction (chemistry)General MedicineMicellar electrokinetic chromatographyShampooAnalytical ChemistryParabenchemistry.chemical_compoundMicellar liquid chromatographyLotionJournal of Chromatographic Science
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