Search results for "aqueous solution"

showing 10 items of 1610 documents

Photocatalytic degradation of nitrophenols in aqueous titanium dioxide dispersion

1991

Abstract The results are reported of an investigation into the photodegradation of nitrophenol isomers carried out in aqueous titania (anatase) dispersions under various experimental conditions. We investigated the influence of various parameters on the photodegradation rate, such as the concentrations of the catalyst, dissolved oxygen and organic compound, and the presence of various anions in the dispersion. A plausible explanation is proposed for the influence of these parameters, both mechanistic and kinetic factors being accounted for. Gas chromatography and mass spectrometry were used as analytical methods in order to determine intermediate products. Spectroscopic methods (UV-vis and …

heterogeneous photocatalysis; TiO2; in-situ IR spectroscopyAnataseAqueous solutionInorganic chemistryGeneral EngineeringPhotochemistryheterogeneous photocatalysischemistry.chemical_compoundNitrophenolReaction rate constantchemistryin-situ IR spectroscopyTitanium dioxidePhotocatalysisTiO2PhotodegradationDispersion (chemistry)Applied Catalysis
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Aqueous-phase reactive species formed by fine particulate matter from remote forests and polluted urban air

2021

In the aqueous phase, fine particulate matter can form reactive species (RS) that influence the aging, properties, and health effects of atmospheric aerosols. In this study, we explore the RS yields of aerosol samples from a remote forest (Hyytiälä, Finland) and polluted urban locations (Mainz, Germany; Beijing, China), and we relate the RS yields to different chemical constituents and reaction mechanisms. Ultra-high-resolution mass spectrometry was used to characterize organic aerosol composition, electron paramagnetic resonance (EPR) spectroscopy with a spin-trapping technique was applied to determine the concentrations of ⚫OH, O2⚫-, and carbon- or oxygen-centered organic radicals, and a …

humic-like substancesAtmospheric ScienceReaction mechanism010504 meteorology & atmospheric sciencesQC1-999Radicalchemistry.chemical_element010501 environmental sciences01 natural scienceswater-soluble pm2.5114 Physical scienceselectron-paramagnetic-resonance11. Sustainabilitypersistent free-radicalsQD1-999Chemical compositionScavenging0105 earth and related environmental sciencespolycyclic aromatic-hydrocarbonsatmospheric hydrogen-peroxideAqueous solutionChemistryhydroxyl radicalsPhysicstransition-metalsParticulatesoxalic-acidAerosolChemistry13. Climate actionEnvironmental chemistryCarbonsecondary organic aerosol
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Chemical Pretreatments of Wood Chips Prior to Alkaline Pulping - A Review of Pretreatment Alternatives, Chemical Aspects of the Resulting Liquors, an…

2015

The chemical industry is being forced to evaluate new strategies for more effective utilization of renewable feedstocks to diminish the use of fossil resources. In this literature review, the integration of both acidic and alkaline pretreatment phases of hardwood and softwood chips with chemical pulping is discussed. Depending on the pretreatment conditions, high-volume sulfur-free fractions with varying chemical compositions can be produced. In case of acidic pretreatments, the major products include carbohydrates (mono-, oligo-, and polysaccharides), whereas under alkaline (i.e., aqueous NaOH) pretreatment conditions, the sulfur-free fractions of aliphatic carboxylic acids, lignin, and ex…

hydrolyysiEnvironmental EngineeringSoftwoodBiochemicalsExtractiveslcsh:BiotechnologyBy-productsCarbohydratesbiokemikaalitBioengineeringRaw materialLigninHydrolysischemistry.chemical_compoundmassanvalmistusextractivesOrganic acidslcsh:TP248.13-248.65organic acidsOrganic chemistryLigninBiorefiningautohydrolysisWaste Management and DisposaldelignificationAqueous solutionPulpingChemistryHydrolysisligniinipretreatmentKraft processAutohydrolysisDelignificationBiorefiningSoda pulpingsivutuotteetbiorefininghiilihydraatitPretreatmentBioResources
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Effect of Mg2+ ions on competitive metal ions adsorption/desorption on magnesium ferrite: Mechanism, reusability and stability studies

2021

Abstract The adsorption behavior of magnesium ferrite in single- and multicomponent metal ions solutions in the presence of Mg2+ ions were studied. A dramatic decrease in the adsorption capacity of magnesium ferrite towards Mn2+, Co2+, and Ni2+ ions for comparison study of single- and multicomponent solutions was established. The affinity of the sorbent in accordance with the maximum sorption capacities increases in the following order Cu2+ > Co2+ > Ni2+ > Mn2+. High efficiency of magnesium ferrite regeneration (~100%) with aqueous solutions of magnesium chloride in the concentration range of 0.001–0.1 M was shown. The low degree of toxic metal ions desorption combined with XRD, IR spectros…

inorganic chemicals021110 strategic defence & security studiesEnvironmental EngineeringAqueous solutionMagnesiumHealth Toxicology and MutagenesisMetal ions in aqueous solutionInorganic chemistry0211 other engineering and technologieschemistry.chemical_elementSorption02 engineering and technology010501 environmental sciences01 natural sciencesPollutionIonAdsorptionchemistryDesorptionEnvironmental ChemistryLeaching (metallurgy)Waste Management and Disposal0105 earth and related environmental sciencesJournal of Hazardous Materials
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Chemical and physical characterization of thermal aggregation of model proteins modulated by zinc(II) and copper(II) ions

2016

BACKGROUND: Metal ions are implicated in protein aggregation processes of several neurodegenerative pathologies, where the protein deposition occurs, and in the biotechnology field like the food technology where many processes in food manufacturing are based on thermal treatments. OBJECTIVE: The influence of Cu2+ or Zn2+ ions on the thermal aggregation process of Bovine beta-lactoglobulin (BLG) and Bovine Serum Albumin (BSA), two protein models, was studied with the aim of delineating the role of these ions in the protein aggregation kinetics and to clarify the related molecular mechanisms. METHODS: The protein structure changes were monitored by Raman spectroscopy, whereas the aggregate gr…

inorganic chemicals0301 basic medicineMetal ions in aqueous solutionKineticsInorganic chemistryBeta-lactoglobulinchemistry.chemical_elementZincProtein aggregation010402 general chemistry01 natural sciencesBovine Serum Albumin (BSA)Beta-lactoglobulin bovine serum albumin (BSA) copper and zinc ionsRaman spectroscopy dynamic light scatteringMetal03 medical and health sciencesProtein structureDynamic light scatteringcopper and zinc ionRadiology Nuclear Medicine and imagingcopper and zinc ionsBovine serum albuminBeta-lactoglobulin; Bovine Serum Albumin (BSA); copper and zinc ions; Raman spectroscopy; dynamic light scatteringbiologydigestive oral and skin physiologydynamic light scattering0104 chemical sciences030104 developmental biologychemistryvisual_artRaman spectroscopyBiophysicsbiology.proteinvisual_art.visual_art_medium
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Properties of a triazolopyridine system as a molecular chemosensor for metal ions, anions, and amino acids.

2006

The characteristics as a chemosensor of the compound 3-methyl-6,8-di(2-pyridyl)-[1,2,3]triazolo[5',1':6,1]pyrido[2,3-]pyrimidine (1) have been analyzed. Interaction with Cu(2+) produces a quenching of the fluorescence, while interaction with Zn(2+) leads to a quenching of the fluorescence followed by a bathochromic shift. The crystal structure of the Zn(1)(H(2)O)(3)(ClO(4))(2) x H(2)O complex shows the coordination of Zn(2+) through the terpyridine moiety. The octahedral site is completed by three water molecules. Interactions of the Zn(2+) complex with the anions sulfate, nitrate, nitrite, and dihydrogenphosphate in ethanol produce hypsochromic shifts and restoration of the fluorescence wh…

inorganic chemicalsAnionsQuenching (fluorescence)ChemistryPyridinesMetal ions in aqueous solutionOrganic ChemistryInorganic chemistryCrystallography X-RayMedicinal chemistrychemistry.chemical_compoundSpectrometry FluorescenceMetalsCationsBathochromic shiftMoleculeMoietyTriazolopyridineHypsochromic shiftSpectrophotometry UltravioletTerpyridineAmino AcidsThe Journal of organic chemistry
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Monoamide Derivatives of EDTA Incorporating Pendent Carboxylates or Pyridyls: Synthesis, Metal Binding, and Crystal Structure of a Dinuclear Ca2+ Com…

2017

EDTA is a powerful, cheap and widely-used chelating unit for a large range of metal ions. To link it covalently to other molecules, the formation of an amide bond using one of the carboxylates is an attractive and simple approach, even though it may compromise metal ion binding as one of the four carboxylate donors is lost. Here we undertake a quantitative study of the metal ion binding of two new mono-amide derivatives of EDTA, namely AmGly1 and AmPy1, featuring an additional coordinating carboxylate or pyridyl group in the amide, respectively. The compounds are conveniently synthesised through alkylation of the tris-t-butyl ester of ethylenediamine-triacetic acid with the appropriate α-ch…

inorganic chemicalsAqueous solution010405 organic chemistryStereochemistryChemistryMetal ions in aqueous solutionGeneral ChemistryCrystal structure010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundAmidePolymer chemistryMoleculeChelationCarboxylateCoordination geometryChemistrySelect
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The different catalytic behaviour in the propane total oxidation of cobalt and manganese oxides prepared by a wet combustion procedure

2013

Abstract Cobalt oxide and manganese oxide catalysts have been prepared through aqueous synthesis using a wet combustion procedure. These materials have been tested as catalysts for the total oxidation of propane. It has been observed a different catalytic behaviour between cobalt and manganese oxides although for both oxides a very high catalytic activity has been obtained. Cobalt oxides prepared by the wet combustion procedure are less reactive than a simple cobalt oxide prepared without the addition of organic acids. However, in the case of manganese oxide the use of organic acids highly increases the catalytic activity. The different catalytic behaviour has been related to the variation …

inorganic chemicalsAqueous solutionChemistryGeneral Chemical EngineeringInorganic chemistrychemistry.chemical_elementGeneral ChemistryManganeseCombustionOxygenRedoxIndustrial and Manufacturing EngineeringCatalysisEnvironmental ChemistryCobalt oxideCobaltChemical Engineering Journal
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Post-synthesis alumination of MCM-41: Effect of the acidity on the HDS activity of supported Pd catalysts

2010

Abstract Siliceous MCM-41 with different amount of alumina, from 0.25 up to 4.0 wt%, were prepared by impregnation of the MCM-41 with aqueous solution of Al(NO) 3 ·9H 2 O. The modified mesoporous silicas were then used as supports for Pd catalysts prepared by wet-impregnation from PdCl 2 precursor. Supports and corresponding Pd catalysts were characterized by XRD, XPS and NH 3 -TPD. The catalytic behavior was tested in the hydrodesulfurization (HDS) reaction of thiophene. An increase of the hydrodesulfurization activity with increasing alumina amount up to 0.5 wt% was observed. On the basis of the acidity change of the support and the structural modification underwent by the deposited palla…

inorganic chemicalsAqueous solutionChemistryProcess Chemistry and TechnologyInorganic chemistrychemistry.chemical_elementHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundMCM-41ThiopheneMesoporous materialHydrodesulfurizationPalladiumApplied Catalysis A: General
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A step forward in the development of superoxide dismutase mimetic nanozymes: the effect of the charge of the surface on antioxidant activity

2019

Two binucleating hezaaza macrocycles containing a pyridinol spacer have been prepared and characterised. Protonation studies indicate the deprotonation of the phenol group at relatively low pH values with the concomitant occurrence of a keto-enolic equilibrium. These ligands readily form binuclear Cu2+ and Zn2+ complexes as denoted by potentiometric and spectroscopic studies. The binding of the metals yields to the ready deprotonation of the phenol with the stabilisation of the keto form that results in complexes of greater stabilities than the analogous ones containing pyridine as spacer instead of pyridine. Mixed Cu2+–Zn2+-complexes were also detected in aqueous solutions containing equim…

inorganic chemicalsAqueous solutionbiologyChemistryGeneral Chemical EngineeringPotentiometric titrationchemistry.chemical_elementProtonation02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMedicinal chemistryCopper0104 chemical sciencesSuperoxide dismutasechemistry.chemical_compoundDeprotonationPyridinebiology.proteinPhenol0210 nano-technologyRSC Advances
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