Search results for "metal ions"

showing 10 items of 282 documents

Studies on mechanism and physico-chemical parameters at the origin of the cement setting II. Physico-chemical parameters determining the coagulation …

1996

The physico-chemical parameters determining the coagulation of cements grains previously identified as the first fundamental process of cement setting have been investigated in diluted suspensions using an adapted granulometric method. The analysis of the influence of the ionic concentration in solution on the coagulation reveals that calcium concentration is the parameter which determines the particle interactions. There exists a minimum critical concentration of calcium ions in solution which is required to occur the coagulation of cement particles and a dispersive effect appears for very high concentrations. The results are discussed in relation with DLVO theory and specific interactions.

CementMaterials scienceMetal ions in aqueous solutionIonic bondingMineralogychemistry.chemical_elementBuilding and ConstructionCalciumChemical engineeringchemistryParticle-size distributionParticleCoagulation (water treatment)DLVO theoryGeneral Materials ScienceCement and Concrete Research
researchProduct

Book Review: Ions in Solution: Basic Principles of Chemical Interactions. By J. Burgess

1989

Chemical engineeringComputational chemistryChemistryMetal ions in aqueous solutionGeneral MedicineGeneral ChemistryChemical interactionCatalysisAngewandte Chemie International Edition in English
researchProduct

Transportation of complexing agents released by pulp and paper industry: A Finnish lake case

1996

Complexing agents (EDTA, DTPA) are used to bind metal ions in pulp and paper industry. Their role will increase significantly when the total chlorine free (TCF) processes will be applied to a larger extent. EDTA and DTPA were analysed in the waters from the southern part of the Lake Saimaa (SE Finland) influenced by the effluents of three pulp and paper mills. The samples were collected at different distances from the points of emission. The results of analyses suggest that EDTA can persist in lake water and is able to propagate for considerable distances, while DTPA can be detected only in the near surroundings of the site of release. Some EDTA was found even in the sampling points that we…

ChemistryHealth Toxicology and MutagenesisNatural waterMetal ions in aqueous solutionPulp (paper)Chlorine.freeengineeringEnvironmental Chemistryengineering.materialPulp and paper industryPollutionEffluentLake waterToxicological & Environmental Chemistry
researchProduct

Host molecules containing electroactive cavities obtained by the molecular assembly of redox-active ligands and metal ions

1995

Self-assembly processes of nickel ions with the redox-active ligand 1,4,8,11-tetra(ferrocenylmethyl)-1,4,8,11-tetraazacyclotetradecane (Fc4cyclam) induces the formation of a redox-active cavity of potential use in electrocatalysis.

ChemistryLigandMetal ions in aqueous solutionInorganic chemistryMolecular MedicineMoleculeRedox activeNickel ionsElectrocatalystCombinatorial chemistryJ. Chem. Soc., Chem. Commun.
researchProduct

Postsynthetic Improvement of the Physical Properties in a Metal-Organic Framework through a Single Crystal to Single Crystal Transmetallation

2015

As ingle crystal to single crystal transmetallation process takes place in the three-dimensional (3D) metal- organic framework (MOF) of formula Mg II 2{Mg II 4(Cu II 2- (Me3mpba)2)3}·45 H2 O( 1 ;M e 3mpba 4¢ = N,N'-2,4,6-trimethyl- 1,3-phenylenebis(oxamate)). After complete replacement of the Mg II ions within the coordination network and those hosted in the channels by either Co II or Ni II ions, 1 is transmetallated to yield two novel MOFs of formulae Co2 II {Co II 4(Cu II 2(Me3- mpba)2)3}·56 H2 O( 2 )a nd Ni2 II {Ni II 4(Cu II 2(Me3mpba)2)3}· 54 H2 O( 3). This unique postsynthetic metal substitution affords materials with higher structural stability leading to enhanced gas sorption and m…

ChemistryLigandStereochemistryMetal ions in aqueous solutionSupramolecular chemistryGeneral MedicineGeneral ChemistryCatalysisMetalCrystalTransmetalationCrystallographyvisual_artYield (chemistry)visual_art.visual_art_mediumSingle crystalAngewandte Chemie International Edition
researchProduct

Electrochemical Detection of High Oxidation States of Chromium( IV and V ) in Chromium‐Doped Cassiterite and Tin‐Sphene Ceramic Pigmenting Systems

2006

Solid-state electrochemistry is applied to detect the presence of chromium centres with high oxidation states in chromium-doped cassiterite and tin-sphene ceramic pigmenting systems. Voltammetric data indicate that CrV and CrIV centres with different coordinative arrangements exist in the studied materials, and yield proton-assisted reduction processes at +0.95, +0.42 AgCl/Ag in contact with 0.50 M H2SO4. Electrochemical measurements are correlated with spectroscopic data. The CrIV and CrV metal ions display a significant light-driven electrocatalytic effect on the oxidation of 1,4-dihydrobenzoquinone and Fe(CN)64– ions that involves the formation of surface-confined adducts. (© Wiley-VCH V…

ChemistryMetal ions in aqueous solutionInorganic chemistryDopingCassiteritechemistry.chemical_elementengineering.materialElectrochemistryInorganic ChemistryChromiumvisual_artvisual_art.visual_art_mediumengineeringCeramicTinVoltammetryEuropean Journal of Inorganic Chemistry
researchProduct

Selective CO2 adsorption by a triazacyclononane-bridged microporous metal-organic framework.

2011

Metal-organic frameworks constructed by self-assembly of metal ions and organic linkers have recently been of great interest in the preparation of porous hybrid materials with a wide variety of functions. Despite much research in this area and the large choice of building blocks used to fine-tune pore size and structure, it remains a challenge to synthesise frameworks composed of polyamines to tailor the porosity and adsorption properties for CO(2). Herein, we describe a rigid and microporous three-dimensional metal-organic framework with the formula [Zn(2)(L)(H(2)O)]Cl (L=1,4,7-tris(4-carboxybenzyl)-1,4,7-triazacyclononane) synthesised in a one-pot solvothermal reaction between zinc ions a…

ChemistryMetal ions in aqueous solutionOrganic ChemistryInorganic chemistrySorptionGeneral ChemistryMicroporous materialCatalysisAdsorptionChemical engineeringMetal-organic frameworkGas separationHybrid materialSelectivityChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

Komplexierung von Übergangsmetall-Ionen mit substituierten Azamakrocyclen: Induktion columnarer Mesophasen durch molekulare Erkennung

1991

ChemistryPolymer chemistryMesophaseGeneral MedicineTransition metal ionsAngewandte Chemie
researchProduct

Preparation and characterization of organofunctionalized bentonite clay bearing aminophosphonic groups in heavy metal uptake

2019

Abstract Bentonite (Bnt) with covalently immobilized N-propylaminodi(methylenephosphonic) groups (Bnt-ADPA) was obtained through a two-step synthesis including aminosilanization and phosphorylation of resulting aminobentonite through Moedritzer-Irani reaction. The grafting of an aminosilane layer in the interplanar space of the bentonite was investigated by XRD, and the presence of N and P-containing groups was confirmed by FTIR, 31P and 29Si MAS NMR. The immobilization of the organic functional groups increased the interplanar distance in bentonite matrix at 52% that essentially improved filtration properties compared to raw bentonite. The number of surface acid groups was evaluated to 0.8…

ChemistryProcess Chemistry and TechnologyMetal ions in aqueous solution02 engineering and technology010501 environmental sciences021001 nanoscience & nanotechnologyGrafting01 natural sciencesPollutionMatrix (chemical analysis)MetalAdsorptionCovalent bondvisual_artBentonitevisual_art.visual_art_mediumChemical Engineering (miscellaneous)Fourier transform infrared spectroscopy0210 nano-technologyWaste Management and Disposal0105 earth and related environmental sciencesNuclear chemistryJournal of Environmental Chemical Engineering
researchProduct

Surface characterisation of metal ions loaded TiO2 photocatalysts: structure–activity relationship

2004

Abstract Transition metal loaded TiO 2 powders were characterised and tested for the photodegradation of some organic acids. Both Lewis and Bronsted surface acid sites were present in the samples containing large amounts of Mo, V and W. The Bronsted sites are associated to the presence of the transition metals as they do not exist in the unloaded support, and in particular to the presence of these metals in high oxidation states. The trend of the pzc values of the various powders matches rather well both with the surface acidity of the samples experimentally determined by NH 3 adsorption and with a scale of acidity/basicity for bulk binary oxides. XPS investigation indicates that only the p…

ChemistryProcess Chemistry and TechnologyMetal ions in aqueous solutionInorganic chemistryCatalysischemistry.chemical_compoundAdsorptionTransition metalPhotocatalysisReactivity (chemistry)Point of zero chargePhotodegradationGeneral Environmental ScienceBenzoic acidApplied Catalysis B: Environmental
researchProduct