Search results for "Aqueous solution"

showing 10 items of 1610 documents

Amphiphilic Polysaccharide Block Copolymers for pH-Responsive Micellar Nanoparticles

2017

A full polysaccharide amphiphilic block copolymer was prepared from end group-functionalized dextrans using copper-mediated azide-alkyne click chemistry. Sufficient modification of the reducing end in both blocks was achieved by microwave-enhanced reductive amination in a borate-buffer/methanol solvent system. The combination of a hydrophilic dextran block with a hydrophobic acetalated dextran block results in an amphiphilic structure that turns water-soluble upon acid treatment. The material has a low critical micelle concentration and self-assembles in water to spherical micellar nanoparticles. The formed nanoparticles have a narrow size distribution below 70 nm in diameter and disassembl…

AzidesPolymers and PlasticsNanoparticleBioengineering02 engineering and technology010402 general chemistry01 natural sciencesReductive aminationBiomaterialsSurface-Active Agentschemistry.chemical_compoundAmphiphileMaterials ChemistryCopolymerOrganic chemistryMicrowavesMicellesAqueous solutionChemistryDextransHydrogen-Ion Concentration021001 nanoscience & nanotechnology0104 chemical sciencesDextranChemical engineeringAlkynesCritical micelle concentrationClick chemistryNanoparticlesClick Chemistry0210 nano-technologyHydrophobic and Hydrophilic InteractionsCopperBiomacromolecules
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Utilization of waste sodium sulfate from battery chemical production in neutral electrolytic pickling

2021

Abstract Several industrial activities produce metal sulfates, which are controlled by strict limitations for wastewater concentrations of sulfate. One emerging area where these activities occur is the production of lithium-ion battery chemicals in which sodium sulfates are formed because of cathode precursor co-precipitation. Several solutions for sulfate removal exist, but one option is to reuse the sulfate side stream in other processes to increase circular economy and atom efficiency. In this paper, the reuse of sodium sulfate solution in a steel industry pickling solution is considered. Neutral electrolytic pickling experiments were carried out to compare the pickling behavior of the e…

Battery (electricity)Renewable Energy Sustainability and the EnvironmentStrategy and ManagementMetal ions in aqueous solutionSodiumInorganic chemistrychemistry.chemical_elementElectrolyteIndustrial and Manufacturing Engineeringchemistry.chemical_compoundchemistryReagentPicklingSodium sulfateSulfateGeneral Environmental ScienceJournal of Cleaner Production
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Silver(I), Copper(I) and Copper(II) Complex of the New N,Se-Chelate Ligand 2-Phenylselenomethyl-1H-benzimidazole: Electrochemistry and Structure

2009

Abstract. 2-Phenylselenomethyl-1H-benzimidazole (psbi) can form complexes in 2:1 ratio with coinage metal ions. Crystal structure analysis revealed a flattened metal coordination for [AgI(psbi)2](BF4) (1), approaching a distorted planar arrangement with weak Ag-Se bonds (d > 2.9 A) and confirmed as energy minimum by DFT calculations. The typical Jahn-Teller system [CuII(psbi)2Cl2] (2) exhibits a planar CuN2Cl2 core with weak Se---Cu---Se axial ligation (3.2944(8) A Cu--Se distance). The oxygen-sensitive compound [CuI(psbi)2](BF4) (3) exhibits electrochemically reversible oxidation in contrast to the silver(I) analogue 1.

BenzimidazoleLigandMetal ions in aqueous solutionInorganic chemistrychemistry.chemical_elementCrystal structureElectrochemistryCopperInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryvisual_artvisual_art.visual_art_mediumChelationZeitschrift für anorganische und allgemeine Chemie
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Photocatalytic oxidation mechanism of benzonitrile in aqueous suspensions of titanium dioxide

2007

Abstract The photocatalytic oxidation of benzonitrile was carried out in aqueous suspensions (pH 11) of commercial polycrystalline TiO 2 (Merck and Degussa P25) irradiated by ultraviolet light. The rate of decomposition was dependent on the concentration of benzonitrile and followed a pseudo-first order kinetics. The complete mineralization of a 0.70 mM benzonitrile solution was achieved in ca. 8 h by using TiO 2 Degussa P25, whereas the substrate was only partially mineralized even after 14 h of irradiation in the presence of TiO 2 Merck. The final oxidation products were carbonate and nitrate. The appearance and the evolution of organic and inorganic intermediate species were also investi…

Benzonitrilechemistry.chemical_compoundAqueous solutionchemistryTitanium dioxideUltraviolet lightPhotocatalysisSubstrate (chemistry)General ChemistryMineralization (soil science)PhotochemistryCatalysisCatalysisCatalysis Today
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Coordinating properties of the Cephalexine antibiotic. A potentiometric study of the complexes formation between Cephalexine and Co(II), Ni(II) and C…

1989

Abstract The formation of complexes between Co(II), Ni(II) and Cu(II) with Cephalexine has been investigated using potentiometric techniques. The stability constants of the complexes formed were calculated using the non-linear least-squares computer program SUPERQUAD. The obtained values were: Co(II) logβ1=2.40, logβMLOH=8.89; Ni(II) logβ1=2.80, logβ2=5.10, logβML2OH=12.09; Cu(II) logβ1=4.094 (25 °C, 0.1 M KNO3). The compound [Ni(CEX)(OH2)4]BPh4 has been synthesized and characterized by electronic, IR and NMR spectroscopies as well as by magnetic measurements. From these studies it is proposed that the Cephalexinate anion acts as a bidentate ligand and is bound to the metal ion through the …

Bicyclic moleculeChemistryMetal ions in aqueous solutionPotentiometric titrationInorganic chemistryProtonationIonInorganic ChemistryMetalCrystallographyvisual_artMaterials Chemistryvisual_art.visual_art_mediumSide chainChemical stabilityPhysical and Theoretical ChemistryInorganica Chimica Acta
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Cu2+and AMP complexation of enlarged tripodal polyamines

2006

The synthesis, characterization, Cu2+ coordination and interaction with AMP of three tripodal polyamines are reported. The polyamines are based on the structure of the tetraamine (tren) which has been enlarged with three propylamino functionalities (TAL), with a further anthrylmethyl fragment at one of its terminal primary nitrogens (ATAL) or with naphthylmethyl fragments at its three ends (N3TAL). The protonation constants of all three polyamines show that at pH 6, all six primary and secondary nitrogen atoms in the arms are protonated. The interaction with Cu2+ and AMP (adenosine-5′-monophosphate) has been studied by potentiometric, UV-Vis, ESI-MS spectroscopy and NMR techniques. pH-Metri…

Binding SitesAqueous solutionMolecular StructureStereochemistryChemistrySpectrum AnalysisPotentiometric titrationProtonationAdenosine MonophosphateAdductInorganic ChemistryParamagnetismPolyaminesPotentiometrySpectroscopyTernary operationCopperStoichiometryDalton Trans.
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Calorimetric and viscosimetric investigation of the interaction between α,β-polyasparthydrazide and sodium dodecyl sulfate micelles

1993

Abstract The interaction between α,β-polyasparthydrazide (PAHy) and sodium dodecyl sulfate (SDS) micelles in aqueous solution was investigated by calorimetry and viscosimetry. The dependence of the enthalpic effect due to this interaction upon the surfactant concentration was rationalized in terms of a progressive binding of SDS micelles to the polymeric backbone. The analysis of the calorimetric data allow evaluation of the binding ability of SDS micelles to the polymeric chain. The viscosimetric behavior of SDS plus PAHy aqueous solutions, discussed in terms of the parameter F [F = ηrel(PAHy) + ηrel(PAHy) − ηrel(SDS+PAHy)], confirms the occurence of the interaction between SDS micelles an…

Binding abilitychemistry.chemical_compoundChromatographyAqueous solutionPulmonary surfactantchemistryPolymer chemistryPharmaceutical ScienceCalorimetrySodium dodecyl sulfateMicelleDosage formMacromoleculeInternational Journal of Pharmaceutics
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The effect of N-tetradecyl-N,N-dimethylamine oxide micelles on the kinetics of the electron transfer reaction of Ce(IV) with substituted malonic acids

2009

Abstract The kinetics of the oxidation of malonic acid and (its substituted compounds, methyl-, ethyl-, butyl- and benzyl-malonic acid) by ceric ions has been studied at 20.0 °C in the absence and the presence of the surfactant N-tetradecyl-N,N-dimethylamine oxide (C 14 DMAO). The addition of increasing amounts of C 14 DMAO influences the rate of the redox process to an extent that significantly depends on the hydrophobicity of the reducing species. The reactivity data together with the estimated binding constants and the standard transfer free energies of the malonic acids from water to the micelles suggest that the malonic acid is confined to the aqueous pseudo-phase while for the other s…

Binding constant; {C14DMAO}; Malonic acids; Redox polymerization{C14DMAO}Aqueous solutionChemistryStereochemistryKineticsBinding constantMalonic acidsMalonic acidRedoxMedicinal chemistryMicelleC14DMAO Binding constant Malonic acids Belousov–Zhabotinsky reaction Redox polymerizationchemistry.chemical_compoundElectron transferRedox polymerizationColloid and Surface ChemistryBinding constant; C14DMAO; Malonic acids; Redox polymerizationC14DMAOReactivity (chemistry)DimethylamineSettore CHIM/02 - Chimica Fisica
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Film-forming process and biocide assessment of high-molecular-weight chitosan as determined by combined ATR-FTIR spectroscopy and antimicrobial assay…

2006

This pioneering study reported about the film-forming properties of high-molecular-weight chitosan as followed in situ by attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, and has implications in fields such as biomedical, pharmaceutical, packaging, and coating applications. From the results, it was observed that immediately after dissolution in an acetic acid aqueous solution and subsequent casting over the ATR crystal, the formed carboxylate antimicrobial (-NH3+ -OOCH) species are not stable in the film formulation and become reduced over time; further assays confirmed previous research, which suggested that the presence and stability of these groups is stron…

BiocideChitosanAqueous solutionBacteriaOrganic ChemistryBiophysicsGeneral Medicineengineering.materialAntimicrobialBiochemistryAnti-Bacterial AgentsBiomaterialsChitosanchemistry.chemical_compoundchemistryAttenuated total reflectionPolymer chemistrySpectroscopy Fourier Transform InfraredengineeringBiopolymerCarboxylateFourier transform infrared spectroscopyNuclear chemistryBiopolymers
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Spectroscopic study of the loading of cationic porphyrins by carbon nanohorns as high capacity carriers of photoactive molecules to cells

2019

Carbon nanomaterials are attractive candidates for drug delivery due to their high surface area, ease of functionalisation and biocompatibility. This work describes the spectroscopic monitoring of the loading capacity of oxidised carbon nanohorns for two cationic porphyrins. Addition of the COOH functionalised carbon nanohorns to both meso-tetra(4-N-methylpyridyl) free base (H2TMPyP4) and platinum (PtTMPyP4) porphyrin in aqueous solution results in hypochromism of the Soret band and quenching of the porphyrin emission. These changes are used to monitor the non-covalent binding interactions with the nanohorn surface and determine the surface loading. The colloidal stability of the nanohorns …

BiocompatibilityNANOTUBESBiomedical Engineeringchemistry.chemical_element02 engineering and technology010402 general chemistryPhotochemistry01 natural scienceschemistry.chemical_compoundpolycyclic compoundsGeneral Materials ScienceDRUG-DELIVERYPHOTOTHERMAL THERAPYNANOMATERIALSQuenching (fluorescence)Aqueous solutionCationic polymerizationFree baseSettore CHIM/06 - Chimica OrganicaGeneral ChemistryGeneral Medicine021001 nanoscience & nanotechnologyPorphyrin0104 chemical scienceschemistry0210 nano-technologyPlatinumCarbonJournal of Materials Chemistry B
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