Search results for "CHROMIUM"

showing 10 items of 494 documents

Nephrotoxic and hepatotoxic effects of chromium compounds in rats

1986

The nephrotoxic, hepatotoxic and cardiotoxic actions of hexavalent chromium compounds, as well as their effects on lung, blood and circulation may contribute to the fatal outcome of chromium intoxication. Although trivalent chromium have been regarded as relatively biologically inert, there are a few salts of chromium III that have been found to be carcinogenic when inhaled, ingested or brought in contact with the tissues. Sensitive persons and industry workers have been subjects of dermatitis, respiratory tract injuries and digestive ulcers due to chromium compounds. In this work, the authors have studied the effect of trivalent and hexavalent chromium compounds on rats measuring the trans…

Chromiuminorganic chemicalsTime FactorsChromium CompoundsHealth Toxicology and Mutagenesischemistry.chemical_elementPharmacologyToxicologyNephrotoxicitychemistry.chemical_compoundChromiumotorhinolaryngologic diseasesAnimalsUreaAspartate AminotransferasesHexavalent chromiumCarcinogenCreatininetechnology industry and agricultureAlanine TransaminaseRats Inbred StrainsGeneral MedicinePollutionRatschemistryBiochemistryBlood chemistryCreatinineKidney DiseasesChromium toxicityChemical and Drug Induced Liver InjuryBulletin of Environmental Contamination and Toxicology
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Removal of trivalent chromium from tannery waste waters using bone charcoal

2002

International audience; The ability of bone charcoal to remove Cr(III) from aqueous solutions by adsorption has been investigated. The adsorbent used was first characterised and then the adsorption was studied as a function of time and amount of charcoal. Tests were carried out with synthetic solutions whose Cr concentrations (500 mg L-1) were similar to those found in some effluents of Moroccan tannery industries. Cr removal efficiencies higher than 90% were obtained at pH 3.5 using 3 g of bone charcoal and a stirring time of about 30 min. Results of Cr removal by all sieved fractions of bone charcoal had shown the same interesting capabilities for Cr(III) retention. The cross interference…

Chromiuminorganic chemicalschemistry.chemical_elementMineralogyIndustrial WasteHydrochloric acid02 engineering and technology010501 environmental sciences01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundChromiumAdsorptionNitric acidSpecific surface areaCharcoal0105 earth and related environmental sciencesAqueous solutionSpectrophotometry Atomic[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyequipment and supplies6. Clean watercarbohydrates (lipids)MoroccochemistrySodium hydroxidevisual_artCharcoalvisual_art.visual_art_mediumMicroscopy Electron ScanningAdsorption0210 nano-technologyWater Pollutants ChemicalNuclear chemistry
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Cathodic reduction of hexavalent chromium coupled with electricity generation achieved by reverse-electrodialysis processes using salinity gradients

2014

Abstract A new approach for the simultaneous generation of electric energy and the treatment of waters contaminated by recalcitrant pollutants using salinity gradients was proposed. Reverse electrodialysis allows for the generation of electric energy from salinity gradients. Indeed, the utilization of different salt concentrations gives a potential difference between the electrodes which allows the generation of electric energy by using suitable electrolytes and an external circuit. The simultaneous generation of electric energy and the treatment of waters contaminated by Cr(VI) was successfully achieved for the first time by reverse electrodialysis processes using salinity gradients and pr…

Cr(VI)ChemistrySupporting electrolyteGeneral Chemical EngineeringElectrolytesalinity gradientVolumetric flow rateSalinitychemistry.chemical_compoundElectricity generationChemical engineeringStack (abstract data type)Waste water treatmentenergy generationEnvironmental chemistryReversed electrodialysisElectrochemistryreverse electrodialisyHexavalent chromium
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Front Cover: Filling the Gap in the Metallacrown Family: The 9‐MC‐3 Chromium Metallacrown (Chem. Eur. J. 13/2021)

2021

CrystallographyChromiumFront coverchemistryOrganic ChemistryStructural integritychemistry.chemical_elementGeneral ChemistryMetallacrownCatalysisChemistry – A European Journal
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Ferromagnetic coupling through the oxalate bridge in heterobimetallic Cr(III)–M(II) (M = Mn and Co) assemblies

2019

Abstract Two novel compounds, {[Cr(pyim)(ox)2]2Mn}n·2nCH3OH (1) and {[Cr(pyim)(ox)2]2Co(H2O)2}·7.5H2O (2) [pyim = 2-(2′-pyridyl)imidazole and H2ox = oxalic acid], were synthesized by using the mononuclear chromium(III) complex PPh4[Cr(pyim)(ox)2]·H2O (PPh4+ = tetraphenylphosphonium) as metalloligand towards the fully solvated manganese(II) (1) and cobalt(II) (2) ions as perchlorate salts. The structure of 1 consists of neutral double chains, with diamond-shaped units sharing the manganese(II) ions with the two other corners being occupied by the chromium(III) ions. The two metal centres in 1 are connected by bis-bidentate oxalate groups, each [CrIII(pyim)(ox)2]− unit being bound to two mang…

Denticity010405 organic chemistryChemistryGeneral Chemical EngineeringOxalic acidchemistry.chemical_elementGeneral ChemistryManganese010402 general chemistry01 natural sciencesOxalate0104 chemical sciencesPerchloratechemistry.chemical_compoundChromiumCrystallographyImidazoleCobaltComptes Rendus Chimie
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Synthesis, Crystal Structure and Magnetic Properties of Three {Cr III Mn II } Heterodimetallic Complexes Based on Heteroleptic Cyanido‐Bearing Cr III…

2017

The use of the heteroleptic [CrIII(AA)(CN)4]- complex as a ligand towards the preformed [MnII(tptz)]2+ and [MnII(pyim)2]2+ species afforded the heterometallic compounds: [MnII(tptz)(H2O)(NO3)(-NC)CrIII(ampy)(CN)3]CH3CN (1), [MnII(tptz)(H2O)(NO3)(-NC)CrIII(phen)(CN)3]H2O (2) and {[MnII(pyim)2][(-NC)Cr(phen)(CN)3]2}3H2O (3) [AA = 2-aminomethylpyridine (ampy) and 1,10-phenanthroline (phen), tptz = 2,4,6-tris(2-pyridyl)-1,3,5-triazine and pyim = 2-(1H-imidazol-2-yl)pyridine]. 1 and 2 are neutral heterodinuclear complexes where a [CrIII(AA)(CN)4]- building block acts as a monodentate ligand through one cyanide group towards a seven coordinate MnII ion. Compound 3 is a neutral heterotrinuclear co…

Denticity010405 organic chemistryChemistryLigandStereochemistryCyanidechemistry.chemical_elementManganeseCrystal structure010402 general chemistry01 natural sciences0104 chemical sciencesIonInorganic ChemistryCrystallographychemistry.chemical_compoundChromiumPyridineEuropean Journal of Inorganic Chemistry
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One-dimensional oxalato-bridged heterobimetallic coordination polymers by using [the [Cr(pyim)(C2O4)2]− complex as metalloligand [pyim = 2-(2′-pyridy…

2019

Abstract Four new coordination polymers based on the use of the [Cr(pyim)(C2O4)2]− species as a metalloligand, namely [LiCr(pyim)(C2O4)2(MeOH)]n (1), {[CaCr2(pyim)2(C2O4)4]·2MeOH}n (2), {[SrCr2(pyim)2(C2O4)4(H2O)]·0.45MeOH·4.55H2O}n (3) and {[CdCr2(pyim)2(C2O4)4]·MeOH}n (4) [pyim = 2-(2′-pyridyl)imidazole] have been synthesized and characterized by elemental analyses, IR spectra and X-ray diffraction on single crystals. Complex 1 is a neutral heterobimetallic chain where the tris(chelated) chromium(III) unit acts as a bis-bidentate ligand towards {Li(MeOH)}+ fragments through its two oxalate ligands, each lithium ion being five-coordinate in a intermediate surrounding between square pyramid…

Denticity010405 organic chemistryLigandchemistry.chemical_element010402 general chemistry01 natural sciencesSquare pyramidal molecular geometry0104 chemical sciencesSquare antiprismInorganic ChemistryCrystallographyChromiumchemistry.chemical_compoundTrigonal bipyramidal molecular geometrychemistryMaterials ChemistryImidazolePhysical and Theoretical ChemistryChirality (chemistry)Inorganica Chimica Acta
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Preparation and crystal structure of the oxalato-bridged CrIII–AgItwo-dimensional compound {Ag3(H2O)[Cr(dpa)(ox)2]3}n·2nH2O (dpa = 2,2′-dipyridylamin…

2004

The reaction of the mononuclear complex [Cr(dpa)(ox)2]− (dpa = 2,2-dipyridylamine) with Ag+ in aqueous solution affords the two-dimensional compound {Ag3(H2O)[Cr(dpa)(ox)2]3}n·2nH2O (1) whose structure has been determined by single-crystal X-ray diffraction. Six crystallographically independent metal atoms (three chromium and three silver atoms) occur in 1. The three [Cr(dpa)(ox)2]− units in 1 act as ligands towards the silver atoms through the two oxalate groups. Each oxalate group acts as bridging ligand adopting five coordination modes: bis-bidentate, bis-bidentate/monodentate (outer), bis-bidentate/monodentate (inner), bidentate/bis-monodentate (outer) and bidentate/monodentate (outer).…

DenticityAqueous solutionInorganic chemistrychemistry.chemical_elementBridging ligandGeneral ChemistryCrystal structureCondensed Matter PhysicsBlock (periodic table)OxalateMetalCrystallographychemistry.chemical_compoundChromiumchemistryvisual_artvisual_art.visual_art_mediumGeneral Materials ScienceCrystEngComm
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Solution and solid state studies with the bis-oxalato building block [Cr(pyim)(C2O4)2]− [pyim = 2-(2′-pyridyl)imidazole]

2013

The preparation, X-ray structure, and variable temperature magnetic study of the new compound {Ba(H2O)3/2[Cr(pyim)(C2O4)2]2}n·9/2nH2O (1) [pyim = 2-(2′-pyridyl)imidazole and C2O42− = dianion of oxalic acid], together with the potentiometric and spectrophotometric studies of the protonation/deprotonation equilibria of the pyim ligand and the ternary complex [Cr(pyim)(C2O4)2]−, are reported herein. The crystal structure of 1 consists of neutral chains, with diamond-shaped units sharing barium(II), with the two other corners occupied by chromium(III). The two metal centers are connected through bis(bidentate) oxalate. Very weak antiferromagnetic interactions between the chromium(III) ions occu…

DenticityInorganic chemistrychemistry.chemical_elementProtonationCrystal structureOxalateAcid dissociation constantchemistry.chemical_compoundChromiumCrystallographyDeprotonationchemistryMaterials ChemistryImidazolePhysical and Theoretical ChemistryJournal of Coordination Chemistry
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[Cr(dmbipy)(ox)2]−: a new bis-oxalato building block for metal assembling. Crystal structures and magnetic properties of XPh4[Cr(dmbipy)(ox)2]·5H2O (…

2010

The synthesis, X-ray structure and variable-temperature magnetic study of new compounds of formula PPh4[Cr(dmbipy)(ox)2]·5H2O (1), AsPh4[Cr(dmbipy)(ox)2]·5H2O (2), {Ba(H2O)2[Cr(dmbipy)(ox)2]2}n·17/2nH2O (3) and {Ag(H2O)[Cr(dmbipy)(ox)2]}n·3nH2O (4) (PPh4+ = tetraphenylphosphonium cation; AsPh4+ = tetraphenylarsonium cation; dmbipy = 4,4′-dimethyl-2,2′-bipyridine; ox2− = oxalate dianion) are reported herein. The isomorphous compounds 1 and 2 are made up of discrete [Cr(dmbipy)(ox)2]− anions, XPh4+ cations [X = P (1) and As (2)] and uncoordinated water molecules. The chromium environment in 1 and 2 is distorted octahedral with Cr–O and Cr–N bond distances varying in the ranges 1.950(2)–1.9782…

DenticityLigandInorganic chemistrychemistry.chemical_elementGeneral ChemistryCrystal structureCondensed Matter PhysicsOxalateMetalChromiumCrystallographychemistry.chemical_compoundchemistryOctahedronvisual_artvisual_art.visual_art_mediumMoleculeGeneral Materials ScienceCrystEngComm
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