Search results for "aqueous solution"

showing 10 items of 1610 documents

High-Resolution Fluorescence Spectra of Airborne Biogenic Secondary Organic Aerosols: Comparisons to Primary Biological Aerosol Particles and Implica…

2021

Aqueous extracts of biogenic secondary organic aerosols (BSOAs) have been found to exhibit fluorescence that may interfere with the laser/light-induced fluorescence (LIF) detection of primary biological aerosol particles (PBAPs). In this study, we quantified the interference of BSOAs to PBAPs by directly measuring airborne BSOA particles, rather than aqueous extracts. BSOAs were generated by the reaction of d-limonene (LIM) or α-pinene (PIN) and ozone (O3) with or without ammonia in a chamber under controlled conditions. With an excitation wavelength of 355 nm, BSOAs exhibited peak emissions at 464–475 nm, while fungal spores exhibited peak emissions at 460–483 nm; the fluorescence intensit…

OzoneAnalytical chemistryautofluorescenceArticlefluorescence spectrachemistry.chemical_compoundAmmoniaOzoneaging processEnvironmental Chemistrysingle-particle measurementRelative humiditybiogenic secondary organic aerosolsParticle SizeAerosolsRange (particle radiation)Air PollutantsAqueous solutionChemistryairborne bioaerosolsGeneral ChemistrySpores FungalFluorescencereal-time detectionAerosolSpectrometry FluorescenceParticleLimoneneEnvironmental sciencetechnology
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Mechanistic aspects of oxalic acid oxidation by photocatalysis and ozonation

2008

Oxalic acid has been oxidised in acidic aqueous solutions (pH 3) using photocatalysis and ozonation alone or coupled. The simultaneous presence of ozone, titanium dioxide and near UV irradiation increases the oxidation rate of oxalic acid to values greater than those deriving from the single contributions of photocatalysis and ozonation. In particular in the present paper ozonation alone, heterogeneous photocatalysis and also combined ozonation with heterogeneous photocatalysis have been used for the oxidation of oxalic acid at acidic pH in the presence of TiO2 Degussa P25. A likely mechanism, able to explain both the homogeneous and heterogeneous processes, is discussed.

OzoneAqueous solutionGeneral Chemical EngineeringOxalic acidInorganic chemistryPhotochemistryElectrochemistrychemistry.chemical_compoundchemistryHomogeneousPhotocatalysis TiO2 Oxidation Oxalic acidTitanium dioxideMaterials ChemistryElectrochemistryPhotocatalysisOxidation rateJournal of Applied Electrochemistry
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Ozone enhanced activity of aqueous titanium dioxide suspensions for photocatalytic oxidation of free cyanide ions

2002

The ozonization and the heterogeneous photocatalytic method are contemporarily applied for the oxidation of free cyanide ions. A batch photoreactor with immersed lamp was used for treating aqueous suspensions containing polycrystalline TiO2 powders irradiated in the near-UV region. Air or ozone–air mixtures were used as oxidation reactants. At the used experimental conditions, the photoreaction proceeds at a measurable rate until low values of cyanide concentration. In the presence of ozone (O3) several parallel reaction routes are contributing to the overall cyanide degradation: (i) homogeneous oxidation by ozone; (ii) heterogeneous catalytic reaction by ozone; (iii) photocatalytic degrada…

OzoneAqueous solutionProcess Chemistry and TechnologyRadicalCyanideInorganic chemistrychemistry.chemical_elementPhotochemistryOxygenCatalysisCatalysischemistry.chemical_compoundchemistryPhotocatalysisOzonideGeneral Environmental ScienceApplied Catalysis B: Environmental
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Chemical and photochemical properties of chloroharmine derivatives in aqueous solutions

2015

Thermal and photochemical stability (ΦR), room temperature UV-vis absorption and fluorescence spectra, fluorescence quantum yields (ΦF) and lifetimes (τF), quantum yields of hydrogen peroxide (ΦH2O2) and singlet oxygen (ΦΔ) production, and triplet lifetimes (τT) have been obtained for the neutral and protonated forms of 6-chloroharmine, 8-chloroharmine and 6,8-dichloroharmine, in aqueous media. When it was possible, the effect of pH and oxygen concentration was evaluated. The nature of electronic transitions of protonated and neutral species of the three investigated chloroharmines was established using Time-Dependent Density Functional Theory (TD-DFT) calculations. The impact of all the fo…

PHOTOCHEMICALGeneral Physics and Astronomychemistry.chemical_elementProtonationTriplet lifetime02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesOxygenFluorescence//purl.org/becyt/ford/1 [https]chemistry.chemical_compoundCHLOROHARMINE//purl.org/becyt/ford/1.4 [https]MoleculePhysical and Theoretical ChemistryAqueous solutionSINGLET OXYGENMolecular StructureChemistrySinglet oxygenPhotochemicalSinglet oxygenOtras Ciencias QuímicasTRIPLET LIFETIMECiencias QuímicasWaterHydrogen PeroxideQuímica021001 nanoscience & nanotechnologyPhotochemical Processes0104 chemical sciencesOxygenSolutionsHarmineSpectrometry FluorescenceAtomic electron transitionChloroharmineDensity functional theoryAbsorption (chemistry)0210 nano-technologyCIENCIAS NATURALES Y EXACTAS
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On the nature of macroradicals formed upon radiolysis of aqueous poly(N-vinylpyrrolidone) solutions

2020

In this work we have explored the nature of macroradicals formed upon radiolysis of aqueous poly(N-vinylpyrrolidone) (PVP) solutions using pulse radiolysis, density functional theory (DFT) and literature data. On the basis of literature data on site-specific kinetics of hydrogen abstraction from simple amides and spectra corresponding to specific radical sites on the same amides we have assessed the distribution of H-atom abstraction by `OH radicals from different positions on the pyrrolidone ring and the polymer backbone. Pulse radiolysis experiments performed at different doses per pulse and different PVP concentrations demonstrate that the H-abstracting radiolysis products are not quanti…

PULSE-RADIOLYSISMaterials sciencePulse radiolysisCROSS-LINKINGNanogelsMICROGELSPOLY(ACRYLIC ACID) NANOGELSHYDROXYL RADICALSPhotochemistry01 natural sciences030218 nuclear medicine & medical imaging03 medical and health scienceschemistry.chemical_compoundDELIVERYNanogel0302 clinical medicine0103 physical sciencesMacroradicalRadiationAqueous solution010308 nuclear & particles physicsN-VinylpyrrolidonePulse (physics)ELECTRONSNETWORKSchemistryRadiolysispoly(N-vinyl pyrrolidone)Density functional theoryDensity functional theoryMacroradicalsSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePOLYMERSRADIATION-INDUCED SYNTHESIS
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Hydrodynamics of the cocurrent downflow of a gas and a foaming liquid through a packed bed. Part I. Estimation of the transition boundary between the…

2004

Abstract In the study the results of investigations are presented aimed at determining such values of the operating parameters for which the change of the hydrodynamic regime occurs from the gas continuous flow (GCF) to the pulsing flow (PF). Nitrogen, helium and argon were used as the gas phase while the liquid phase was formed by the aqueous solutions of the alcohols C 1 –C 4 of the concentrations which ensured the foaming of the system. Thus a wide range of physicochemical properties of the system was covered in the experiments. The present study, as well as Part II, contain a wealth of experimental data which characterise the PF through the packing for the foam-forming systems. It is de…

Packed bedAqueous solutionArgonProcess Chemistry and TechnologyGeneral Chemical EngineeringEnergy Engineering and Power Technologychemistry.chemical_elementBoundary (topology)ThermodynamicsGeneral ChemistryNitrogenIndustrial and Manufacturing EngineeringchemistryFlow (mathematics)Flow mapHeliumChemical Engineering and Processing: Process Intensification
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Solution Properties of Poly-Electrolytes. XI. Adsorption Effects in Aqueous Size-Exclusion Chromatog-Raphy of Polyanions

1994

Abstract Elution profiles of a series of polymer standards such as sodium poly(styrene sulphonate), poly(acrylic acid) and poly(L-glutamic acid) have been obtained from size-exclusion chromatography experiments using separately two types of hydrophilic supports. A variety of mobile phase compositions have been performed to enhance adsorption effects in order to study how this phenomenon can affect to the chromatographic separation mechanism of polyanions. Distribution coefficient values, in general greater than unity, have served to quantify the adsorption effect, as well as to analyze their dependence on eluent ionic strength, on the ionic groups of the support and on the chemical nature a…

Partition coefficientAqueous solutionAdsorptionChromatographyMolar massChemistryIonic strengthElutionSize-exclusion chromatographyMolecular MedicineIonic bondingJournal of Liquid Chromatography
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The Impact of Humic Substances as Remediation Agents to the Speciation Forms of Metals in Soil

2013

Abstract Humic substances (HS) are the most widespread group of organic substances in natural environment and have high stability. The main terrestrial reserves are found in the form of naturally occurring ore, peat or lignite. The aim of this paper is to study possibilities to use HS as agents for remediation of contaminated with heavy metals soil and impacts of HS of metal speciation forms in it. It has been proved that HS are able to bind to metal ions and change their speciation forms in soils. The ability to form complexes with metal ions depends on the type of soil, type of metal, as well as concentrations of HS in soil. The study was carried out in experimental conditions and analyti…

PeatChemistryEnvironmental remediationMetal ions in aqueous solutionmedia_common.quotation_subjectHumic acidsRemediationchemistry.chemical_elementContaminationCopperMetalSpeciationGeneral Energyvisual_artEnvironmental chemistrySoil watervisual_art.visual_art_mediumSpeciation analysisHeavy metal complexesmedia_commonAPCBEE Procedia
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Peptidomimetics – An infinite reservoir of metal binding motifs in metabolically stable and biologically active molecules

2020

The involvement of metal ions in interactions with therapeutic peptides is inevitable. They are one of the factors able to fine-tune the biological properties of antimicrobial peptides, a promising group of drugs with one large drawback - a problematic metabolic stability. Appropriately chosen, proteolytically stable peptidomimetics seem to be a reasonable solution of the problem, and the use of D-, β-, γ-amino acids, unnatural amino acids, azapeptides, peptoids, cyclopeptides and dehydropeptides is an infinite reservoir of metal binding motifs in metabolically stable, well-designed, biologically active molecules. Below, their specific structural features, metal-chelating abilities and anti…

PeptidomimeticMetal ions in aqueous solutionAntimicrobial peptidesMetal binding sites010402 general chemistryPeptides Cyclic01 natural sciencesBiochemistryInorganic ChemistryPeptoidsHumansMoleculeAmino AcidsChelating Agentschemistry.chemical_classificationBinding SitesBacteria010405 organic chemistryMetal bindingStereoisomerismBiological activityAntimicrobialCombinatorial chemistryAnti-Bacterial Agents0104 chemical sciencesAmino acidchemistryAntimicrobial peptidesPeptidomimeticsJournal of Inorganic Biochemistry
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Complex formation of Tb3+ with glycolate, D-gluconate and α-isosaccharinate in neutral aqueous perchlorate solutions

2003

Summary An electromigration technique was used for measurements of metal-ligand formation constants of non-carrier-free 160Tb3+ with glycolate, D-gluconate and α-isosaccharinate ligands. The overall ion mobilities of Tb at different concentrations of the ligands were measured in chemically inert perchlorate solutions (pH 7 and T= 298.1K) with an overall ionic strength μ = 0.1. The stepwise stoichiometric stability constants are: Tb3+/glycolate: log K 1=2.72(18), log K 2=1.73(19), log K 3= 1.12(17), Tb3+/D-gluconate: log K 1=2.96(11), log K 2=2.60(11), log K 3=1.13(9), Tb3+/α-ISA: log K 1=3.07(8), log K 2 = 2.69(11), log K 3 = 1.80(12).

Perchloratechemistry.chemical_compoundAqueous solutionchemistryD-gluconateIonic strengthStability constants of complexesStereochemistryComplex formationPhysical chemistryPhysical and Theoretical ChemistryStoichiometryIonRadiochimica Acta
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