Search results for "DSO"

showing 10 items of 1609 documents

Cadmium and Copper Removal by a Granular Activated Carbon in Laboratory Column Systems

2000

Single and competitive removal of Cd and Cu from aqueous solutions by using Darco 12–20 mesh granular activated carbon in column systems has been investigated. Seven experiments modifying the initial pH and the flow rate were performed. Results showed the efficiency of activated carbon as a sorbent for both metals. pH is shown to be the decisive parameter on metal removal in the column; metal removal increases when the influent pH value is raised. The influence of the flow rate for the experimental conditions is negligible. Batch adsorption and column data are compared. Column modeling assuming local equilibrium and rate-controlled pore diffusion was performed.

CadmiumAqueous solutionSorbentChemistryProcess Chemistry and TechnologyGeneral Chemical EngineeringDiffusionInorganic chemistrychemistry.chemical_elementFiltration and SeparationGeneral ChemistryCopperVolumetric flow rateAdsorptionmedicineActivated carbonmedicine.drugSeparation Science and Technology
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Cadmium and Zinc Adsorption onto Activated Carbon: Influence of Temperature, pH and Metal/Carbon Ratio

1996

The adsorption characteristics of cadmium and zinc onto a granular activated carbon were studied. Cadmium and zinc removals increased on raising pH and temperature, and decreased on raising the molar metal/carbon ratio. The adsorption processes were modelled using the surface complex formation (SCF) Triple Layer Model (TLM) with an overall bidentate species. A dependence of the SCF constant on pH, the molar metal/carbon ratio and temperature was observed, and a correlation for log K ads was determined. The SCF model successfully predicted cadmium and zinc removals.

CadmiumDenticityAqueous solutionRenewable Energy Sustainability and the EnvironmentChemistryGeneral Chemical EngineeringOrganic ChemistryInorganic chemistrychemistry.chemical_elementZincPollutionInorganic ChemistryMetalFuel TechnologyAdsorptionvisual_artvisual_art.visual_art_mediummedicineWaste Management and DisposalCarbonBiotechnologyActivated carbonmedicine.drugJournal of Chemical Technology & Biotechnology
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Sorption of thallium(I) ions by peat.

2013

The increasing industrial use of thallium has raised the need for removal of this highly toxic element from wastewater. Thallium is more toxic than cadmium, copper, zinc, lead and mercury and as it is easily accumulated in humans, animals and plants, it poses a threat to both the environment and human health. Peat has been used as an effective, relatively cheap and easily available sorbent to treat waters containing heavy metals. In this study, peat was characterized and used as sorbent for the removal of Tl(I) ions from aqueous solution. The effect of initial Tl(I) concentration, pH, contact time, temperature and ionic strength was studied in batch mode. The maximum sorption capacity of pe…

CadmiumEnvironmental EngineeringAqueous solutionSorbentOsmolar ConcentrationTemperaturechemistry.chemical_elementSorptionZincHydrogen-Ion ConcentrationMercury (element)Water PurificationKineticsSoilchemistryModels ChemicalIonic strengthEnvironmental chemistryThalliumAdsorptionThalliumWater Pollutants ChemicalWater Science and TechnologyNuclear chemistryWater science and technology : a journal of the International Association on Water Pollution Research
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Effect of pH, cation concentration and sorbent concentration on cadmium and copper removal by a granular activated carbon

1999

The single adsorption of cadmium and copper from aqueous solutions has been investigated on Darco 12-20 mesh granular activated carbon for a wide range of experimental conditions: pH, metal concentration and carbon concentration. The results showed the efficiency of the activated carbon as sorbent for both metals. Metal removal increases on raising pH and carbon concentration, and decreases on raising the initial metal concentration. The adsorption processes have been modelled using the surface complex formation (SCF) Triple Layer Model (TLM) with a single surface bidentate species or with an overall surface species with fractional stoichiometry. Bidentate stoichiometry considering pH, meta…

CadmiumSorbentRenewable Energy Sustainability and the EnvironmentGeneral Chemical EngineeringOrganic ChemistryInorganic chemistrychemistry.chemical_elementConcentration effectPollutionCopperInorganic ChemistryFuel TechnologyAdsorptionchemistrymedicineFreundlich equationWaste Management and DisposalCarbonBiotechnologyActivated carbonmedicine.drugJournal of Chemical Technology & Biotechnology
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Where Is the Most Hydrophobic Region? Benzopurpurine Self-Assembly at the Calcite–Water Interface

2017

Control of molecular self-assembly at solid–liquid interfaces is challenging due to the complex interplay between molecule–molecule, molecule–surface, molecule–solvent, surface–solvent, and solvent–solvent interactions. Here, we use in-situ dynamic atomic force microscopy to study the self-assembly of Benzopurpurine 4B into oblong islands with a highly ordered inner structure yet incommensurate with the underlying calcite (10.4) surface. Molecular dynamics and free energy calculations provide insights by showing that Benzopurpurine 4B molecules do not anchor to the surface directly but instead assemble on top of the second hydration layer. This seemingly peculiar behavior was then rationali…

CalciteChemistryAtomic force microscopy02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology53001 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsHydrophobeMolecular dynamicschemistry.chemical_compoundCrystallographyGeneral EnergyAdsorptionChemical physicsMoleculeSelf-assemblyPhysical and Theoretical Chemistry0210 nano-technologyLayer (electronics)The Journal of Physical Chemistry C
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Stabilization of Polar Step Edges on Calcite (10.4) by the Adsorption of Congo Red

2015

In this work, we present the stabilization of polar step edges along the [010] direction of calcite (10.4) by the presence of a water-soluble organic molecule, namely Congo Red. While characteristic etch pits are observed on the surface in the absence of the additive, no etch pits can be found in the presence of the additive. Using atomic force microscopy, we can directly follow the restructuring of the surface. Upon addition of Congo Red, the charge-neutral step edges confining the characteristic etch pits vanish, while polar step edges along the [010] direction appear on the surface, which are entirely decorated by well-ordered molecular islands of the additive. After the restructuring ha…

CalciteChemistryDirect evidenceAtomic force microscopyMineralogySurfaces and InterfacesCondensed Matter Physics530Congo redchemistry.chemical_compoundAdsorptionChemical physicsElectrochemistryPolarStep edgesMoleculeGeneral Materials ScienceSpectroscopy
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Deposition order controls the first stages of a metal-organic coordination network on an insulator surface

2016

| openaire: EC/FP7/610446/EU//PAMS We report on first stages toward the formation of a surface-confined metal-organic coordination network (MOCN) by sequential deposition of biphenyl-4,4′-dicarboxylic acid and iron atoms on the surface of a bulk insulator, calcite (10.4). The influence of the deposition order on the structure formation is studied by noncontact atomic force microscopy operated in ultrahigh vacuum at room temperature. It is found that sequential deposition facilitates MOCN formation when the organic linker molecules are first adsorbed on the surface, followed by iron deposition. This observation is explained by first-principles computations, indicating that the metal-molecule…

CalciteStructure formationta114Atomic force microscopyIron deposition02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology53001 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistry.chemical_compoundGeneral EnergyAdsorptionchemistryChemical physicsLattice (order)Coordination networkMoleculePhysical and Theoretical Chemistry0210 nano-technologyJournal of Physical Chemistry C
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Clear signature of the (2 x 1) reconstruction of calcite (1014).

2010

Calcite is a mineral of fundamental importance that plays a crucial role in many fields of research such as biomineralization, biomolecule adsorption, and reactivity as well as industrial and daily life applications. Consequently, the most stable cleavage plane of calcite has been studied extensively using both direct imaging techniques such as atomic force microscopy as well as spectroscopic and diffraction techniques. Several surface structures have been reported for the (10 (1) over bar4) cleavage plane of calcite differing from the simple bulk-truncated structure and an ongoing controversy exists in literature whether the cleavage plane exhibits a (2 x 1) reconstruction or not. We study…

CalciteSurface (mathematics)chemistry.chemical_classificationDiffractionMineralMaterials scienceBiomoleculeSurfaces and InterfacesCondensed Matter PhysicsMicroscopy Atomic Force530Calcium Carbonatechemistry.chemical_compoundCrystallographyAdsorptionCalcium carbonatechemistryChemical physicsElectrochemistryGeneral Materials ScienceSpectroscopyBiomineralizationLangmuir : the ACS journal of surfaces and colloids
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Zirconium and hafnium fractionation and distribution of Rare Earth Elements in neutral–alkaline waters: Case study of Lake Van hydrothermal system, T…

2021

International audience; We investigated the distribution of Zr, Hf, and rare earth elements (REE) as the sum of lanthanides plus Y in the hydrothermal system in the Lake Van area of south-eastern Turkey. This system is characterised by water with variable pH in alkaline conditions resulting from hydrothermal CO2 upraise and neoformation of calcite minerals in near equilibrium with the interacting waters. Zr, Hf, and REE determinations were carried out for aqueous phases and suspended solids in lake water and surrounding thermal springs. We found that dissolved Hf is partitioned relative to Zr during calcite formation and that such fractionation is a function of the Ca2+ activity in warm wat…

CalciteZirconiumAqueous solutionTurkeyChemistryInorganic chemistryCarbonate mineralschemistry.chemical_elementAlkaline lakes REE Turkey Zr/Hf ratioAuthigenicFractionation010501 environmental sciences010502 geochemistry & geophysicsREEAlkaline lakes01 natural sciences6. Clean waterHydrothermal circulationchemistry.chemical_compoundAdsorption[SDU.STU.GC]Sciences of the Universe [physics]/Earth Sciences/GeochemistryGeochemistry and PetrologyZr/Hf ratioEconomic Geology0105 earth and related environmental sciencesJournal of Geochemical Exploration
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Changes in surface stress at the liquid/solid interface measured with a microcantilever

2000

Abstract The bending of microfabricated silicon nitride cantilevers was used to determine surface stress changes at solid–liquid interfaces. The radius of curvature of the bent cantilever is directly proportional to changes in the differential surface stress between its opposite sides. To demonstrate the possibilities and limitations of the technique, cantilevers coated on both sides with gold and densely packed monolayers of different thiols were put in a constant flow of aqueous electrolyte solution and the deflection was measured using a optical lever technique. Changes in the surface stress for the different thiol monolayers due to specific proton adsorption are presented. Possible appl…

CantileverChemistryGeneral Chemical EngineeringSurface stressMineralogyBendingchemistry.chemical_compoundAdsorptionSilicon nitrideDeflection (engineering)MonolayerElectrochemistryComposite materialBiosensorElectrochimica Acta
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