Search results for "Iodide"

showing 10 items of 405 documents

Observations on the use of a sulfuric acid medium for As(V) to As(III) reduction in lodimetric titrations: Application to the determination of total …

1991

Abstract The use of a sulfuric rather than a hydrochloric acid medium for the reduction of As(V) to As(III) by iodide is proposed. Optimum conditions of acid concentration, amount of sodium hydroxide, and time and temperature are established to achieve quantitative reduction. The optimized reduction procedure was applied to the iodimetric determination of total arsenic and compared to a procedure that employs a hydrochloric acid medium. A systematic error of 0.04% was found for the method with a sulfuric acid medium opposed to 0.05% for the method with a hydrochloric acid medium in the reduction step. The proposed modified iodimetric method has been successfully used with some organic sampl…

chemistry.chemical_classificationAcid concentrationIodideInorganic chemistrychemistry.chemical_elementHydrochloric acidSulfuric acidAnalytical ChemistryReduction (complexity)chemistry.chemical_compoundchemistrySodium hydroxideTitrationSpectroscopyArsenicMicrochemical Journal
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Tungsten oxides as catalysts in selective oxidation

1983

Abstract The reaction of allyl iodide was studied at the surface of four tungsten oxides and molybdenum trioxide. On WO2.95 and MoO3, in which crystallographic shear structures are formed on reduction, acrolein is produced at 300–400 °C, whereas W18O49 and WO2, which do not show this property, are inactive, as is WO3. It is concluded that the transformation of a corner-linked into an edge-linked arrangement of metal-oxygen octahedra provides a facile route for insertion of oxygen into a hydrocarbon molecule.

chemistry.chemical_classificationAllyl iodideAcroleinInorganic chemistrychemistry.chemical_elementTungstenOxygenCatalysisCatalysisMolybdenum trioxidechemistry.chemical_compoundHydrocarbonchemistryMoleculePhysical and Theoretical ChemistryJournal of Catalysis
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The NreA Protein Functions as a Nitrate Receptor in the Staphylococcal Nitrate Regulation System

2013

Staphylococci are able to use nitrate as an alternative electron acceptor during anaerobic respiration. The regulation of energy metabolism is dependent on the presence of oxygen and nitrate. Under anaerobic conditions, staphylococci employ the nitrate regulatory element (Nre) for transcriptional activation of genes involved in reduction and transport of nitrate and nitrite. Of the three proteins that constitute the Nre system, NreB has been characterized as an oxygen sensor kinase and NreC has been characterized as its cognate response regulator. Here, we present structural and functional data that establish NreA as a new type of nitrate receptor. The structure of NreA with bound nitrate w…

chemistry.chemical_classificationAnaerobic respirationStaphylococcusIodideIsothermal titration calorimetryGene Expression Regulation BacterialElectron acceptorCrystallography X-RayResponse ElementsNitrate reductaseNitrate ReductaseProtein Structure SecondaryBacteria Anaerobicchemistry.chemical_compoundResponse regulatorNitratechemistryBiochemistryStructural BiologyMutationBinding siteMolecular BiologyJournal of Molecular Biology
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Electrochemically triggered iodide-vacancy BiOI film for selective extraction of iodide ion from aqueous solutions

2021

Abstract The effective extraction and regeneration of radioactive iodide remains an urgent concern for safe nuclear energy utilization. Herein, we developed a novel electrochemically triggered iodide-vacancy BiOI film, which exhibited excellent I− ion extraction capacity of 328.3 mg·g−1. Especially, due to the ion vacancy trap effect, the film showed high selectivity towards I− ions in the existence of a large number of competitive anions. Additionally, the electrochemically switched ion extraction (ESIE) process with this iodide-vacancy BiOI film possessed fast extraction kinetics and high stability. More importantly, the trapped I− ions were easily desorbed from the film without the secon…

chemistry.chemical_classificationAqueous solutionChemistryExtraction (chemistry)KineticsHigh selectivityInorganic chemistryIodideFiltration and Separation02 engineering and technologySettore ING-IND/27 - Chimica Industriale E Tecnologica021001 nanoscience & nanotechnologyIodide ions Iodide-vacancy BiOI film Electrochemically switched ion extraction Selective extraction Radioactive waterAnalytical ChemistryIonIodide ion020401 chemical engineeringVacancy defect0204 chemical engineering0210 nano-technology
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Microwave-assisted distillation of iodine for the indirect atomic absorption spectrometric determination of iodide in milk samples

2001

To complete these microwave distillation studies, a method for iodide determination in milk-type samples is proposed. The iodide contained in the sample is oxidized to iodine, which is distilled by means of microwave energy and reduced back to iodide. This iodide is combined with Hg(II) and 2,2′-dipyridyl to give an ion pair, which is selectively extracted into IBMK. Mercury is determined in the extract by ETAAS in order to determine iodide. The yield of the distillation process (100%) was evaluated using the Sandell–Kolthoff reaction. In addition, for the solvent extraction, no buffer was needed; 3/5 was the best phase ratio (organic/aqueous); 30 s was the shaking time and the extracts wer…

chemistry.chemical_classificationAqueous solutionChromatographyIodideAnalytical chemistrychemistry.chemical_elementIodineAnalytical Chemistrylaw.inventionLinear rangechemistryAshinglawStandard additionAtomic absorption spectroscopyDistillationSpectroscopyJ. Anal. At. Spectrom.
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Sequestering Ability of Aminopolycarboxylic (APCs) and Aminopolyphosphonic (APPs) Ligands Toward Palladium(II) in Aqueous Solution

2014

The binding capacity of three aminopolycarboxylates [nitrilotriacetic acid (NTA), ethylene-glycol-bis(2-aminoethyl ether)-N,N,N,N-tetraacetic acid (EGTA), and diethylenetriamine-N,N,N,NN-pentaacetic acid (DTPA)] and two aminopolyphosphonates {(1-hydroxyethane-1,1-diyl)bis(phosphonic acid) (HEDP) and [[(phosphonomethyl)imino]bis[2,1-ethanediylnitrilobis(methylene)]] tetrakis-phosphonic acid (DTPP)} toward palladium(II) ion was studied by potentiometric and spectrophotometric titrations at different temperatures (283.15 ≤ T/K ≤ 318.15) and ionic strengths (0.1 ≤ I/mol·dm -3 ≤ 1.0) in NaClO4. The hydrolysis of Pd2+ and the protonation of ligands were always taken into account in the speciation…

chemistry.chemical_classificationAqueous solutionGeneral Chemical EngineeringIodidePotentiometric titrationInorganic chemistryNitrilotriacetic acidchemistry.chemical_elementEtherProtonationGeneral ChemistryMedicinal chemistrycomplex formation Aminopolycarboxylic and aminopolyphosphonic ligands spectrophotometry palladium sequestration.chemistry.chemical_compoundchemistrySettore CHIM/01 - Chimica AnaliticaMethylenePalladium
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Consequences of linking charged and uncharged monomers to binary copolymers studied in dilute solution. Part II: Non-additivity effects in the viscom…

2017

Abstract Copolymers of ethylene oxide (EO) and N,N-dimethyl aminoethyl methacrylate (R) or [2-(methacryloyloxy)ethyl] trimethylammonium iodide (R+) were studied in dilute solution: P ( EO p – b – R n ) ( I ) , P(Rn(1−f) – ran – R+n f) ( II ) , and P ( EO p – b – R n + ) ( III ) ; n and p give the numbers of monomers and f is the degree of charging. For II (variable f) and III (variable n) the effects of charging on the intrinsic viscosities [η] are well described by Boltzmann sigmoids. The deviation of [ η ] from [ η ] add (calculated from the corresponding homopolymer data, assuming additivity of the individual contributions) are quantified by σ = [ η ] / [ η ] add - 1 measuring the segreg…

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsEthylene oxideIntrinsic viscosityOrganic ChemistryIodideGeneral Physics and AstronomyBinary number02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistry.chemical_compoundMonomerchemistryAdditive functionPolymer chemistryMaterials ChemistryCopolymerPhysical chemistry0210 nano-technologyEuropean Polymer Journal
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Bis(N-substituted oxamate)palladate(ii) complexes as effective catalysts for sustainable Heck carbon–carbon coupling reactions in n-Bu4NBr as the sol…

2015

Five bis(oxamato)palladate(II) complexes of the formulae (n-Bu4N)2[Pd(4-Fpma)2] (1), (n-Bu4N)2[Pd(4-Clpma)2] (2), (n-Bu4N)2[Pd(4-Brpma)2] (3), (n-Bu4N)2[Pd(4-Brpma)2]·H2O (3a), (n-Bu4N)2[Pd(4-MeOpma)2] (4) and (n-Bu4N)2[Pd(4-Isopma)2] (5) (n-Bu4N+ = tetra-n-butylammonium, 4-Fpma = N-4-fluorophenyloxamate, 4-Clpma = N-4-chlorophenyloxamate, 4-Brpma = N-4-bromophenyloxamate, 4-MeOpma = N-4-methoxyphenyloxamate and 4-isopma = N-4-isopropylphenyloxamate) have been easily prepared and characterized by spectroscopic methods and the crystal structures of two of them (3a and 4) have been determined by single crystal X-ray diffraction. Each palladium(II) ion in 3a and 4 is four-coordinate with two o…

chemistry.chemical_classificationArylInorganic chemistryIodidechemistry.chemical_elementCrystal structureMedicinal chemistryCoupling reactionCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryBromideIonic liquidPalladiumInorganic Chemistry Frontiers
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Sustainable carbon–carbon bond formation catalyzed by new oxamate-containing palladium(II) complexes in ionic liquids

2013

Abstract New and versatile bis(oxamato)palladate(II) complexes of formula ( n -Bu 4 N) 2 [Pd(2-Mepma) 2 ]·4H 2 O ( 1a ) and ( n -Bu 4 N) 2 [Pd(4-Mepma) 2 ]·2H 2 O·MeCN ( 1b ) ( n -Bu 4 N +  = tetra- n -buthylammonium, 2-Mepma =  N -2-methylphenyloxamate and 4-Mepma =  N -4-methylphenyloxamate) have been synthesized and characterized by spectroscopic methods and single crystal X-ray diffraction. Each palladium(II) ion in 1a and 1b is four-coordinate with two oxygen and two nitrogen atoms from two fully deprotonated oxamate ligands building a centrosymmetric square planar surrounding. Their catalytic role has been investigated for both Heck and Suzuki coupling reactions using a series of aryl…

chemistry.chemical_classificationArylOrganic ChemistryIodidechemistry.chemical_elementBiochemistryMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundchemistrySuzuki reactionCarbon–carbon bondBromideIonic liquidMaterials ChemistryPhysical and Theoretical ChemistryPalladiumJournal of Organometallic Chemistry
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Iodine speciation in rain, snow and aerosols

2008

Iodine oxides, such as iodate, should be the only thermodynamically stable sink species for iodine in the troposphere. However, field observations have increasingly found very little iodate and significant amounts of iodide and soluble organically bound iodine (SOI) in precipitation and aerosols. The aim of this study was to investigate iodine speciation, including the organic fraction, in rain, snow, and aerosols in an attempt to further clarify aqueous phase iodine chemistry. Diurnal aerosol samples were taken with a 5 stage cascade impactor and a virtual impactor (PM<sub>2.5</sub>) from the Mace Head research station, Ireland, during summer 2006. Rain was collected from Austr…

chemistry.chemical_classificationAtmospheric ScienceIodidechemistry.chemical_elementIodineSnowlcsh:QC1-999Aerosollcsh:Chemistrychemistry.chemical_compoundchemistrylcsh:QD1-999Environmental chemistryOrganic matterInductively coupled plasma mass spectrometryRain and snow mixedIodatelcsh:PhysicsAtmospheric Chemistry and Physics
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