Search results for "Inorganic chemist"

showing 10 items of 7340 documents

Novel Porous Carbon Material for the Detection of Traces of Volatile Organic Compounds in Indoor Air

2021

International audience; A highly sensitive and selective silicon-based microanalytical prototype was used to identify a few ppb of volatile organic compounds (VOCs) in indoor air. Herein, a new nonactivated tannin-derived carbon synthesized by an environmentally friendly method, DM2C, a MIL-101(Cr) MOF, and a DaY zeolite were selected for the preconcentration of BTEX compounds (i.e., benzene, toluene, ethylbenzene, and xylenes). Integrating a small amount of these nanoporous solids inside a miniaturized preconcentration unit led to excellent preconcentration performance. By taking advantage of the high adsorption−desorption capacities of the DM2C adsorbent, concentrations as low as 23.5, 30…

indoor air monitoringMaterials scienceInorganic chemistrychemistry.chemical_element02 engineering and technologyBTEX010501 environmental sciences[CHIM.INOR]Chemical Sciences/Inorganic chemistry01 natural sciencesEthylbenzene[SPI.MAT]Engineering Sciences [physics]/Materialschemistry.chemical_compound[SPI]Engineering Sciences [physics]AdsorptionGeneral Materials ScienceRelative humidity[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/MicroelectronicszeoliteBenzene0105 earth and related environmental sciencesMOF[SPI.ACOU]Engineering Sciences [physics]/Acoustics [physics.class-ph]Nanoporousmicroporous materialspreconcentrator[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyToluenehydrophobic carbonchemistry[SDE]Environmental Sciences0210 nano-technologyCarbonminiaturized gas chromatographBTEX
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Equilibrium and structural studies of complexes with a hexadentate ligand containing amide, amine and pyridyl nitrogen donors. Crystal structures of …

2002

A novel potentially hexadentate ligand, 1,8-bis(2-pyridylcarbamoyl)-3,6-diazaoctane (pyctrien) has been synthesised as its tetrahydrochloride salt; its protonation constants and the stability constants of the copper(II) and nickel(II) chelates have been determined by potentiometry. Amide group deprotonation permits the formation of [MLH−1]+ and [MLH−2] species in all cases, whereas the detection of the neutral or the protonated species depends on the nature of the metal ions. The solid complexes of copper, nickel and cobalt with the neutral and the deprotonated ligand have been synthesised and characterised by IR and UV–VIS spectroscopy. The amidic groups are coordinated through the oxygen …

inorganic chemicals010405 organic chemistryLigandInorganic chemistrychemistry.chemical_elementProtonationGeneral Chemistry[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesSquare pyramidal molecular geometry0104 chemical scienceschemistry.chemical_compoundNickelCrystallographyDeprotonationchemistryAmidePyridine[CHIM.COOR]Chemical Sciences/Coordination chemistryCobaltComputingMilieux_MISCELLANEOUS
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Uncapping the N-terminus of a ubiquitous His-tag peptide enhances its Cu2+ binding affinity

2019

Metal complexes with an N-terminally free and N-terminally acetylated polyhistidine region of Echis ocellatus venom, with an interesting His-rich motif present in numerous metal binding proteins from all kingdoms of life (DHDHDHHHHHHPGSSV-NH2 and Ac-DHDHDHHHHHHPGSSV-NH2) show the role of the free amino group in the thermodynamic enhancement of Cu2+, Ni2+ and Zn2+ binding. In the studied sequences, Cu2+ can be coordinated by different sets of imidazole rings, and a 3–10 helix is detected in close proximity of Cu2+ binding sites. The complexes are more stable than those with a typical His6-tag, despite a similar copper(II) coordination mode in both cases.

inorganic chemicals010405 organic chemistryStereochemistryChemistryPeptide sequence tagVenom010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryMetalN-terminuschemistry.chemical_compoundAcetylationvisual_artvisual_art.visual_art_mediumImidazoleBinding siteUncappingDalton Transactions
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Effect of Mg2+ ions on competitive metal ions adsorption/desorption on magnesium ferrite: Mechanism, reusability and stability studies

2021

Abstract The adsorption behavior of magnesium ferrite in single- and multicomponent metal ions solutions in the presence of Mg2+ ions were studied. A dramatic decrease in the adsorption capacity of magnesium ferrite towards Mn2+, Co2+, and Ni2+ ions for comparison study of single- and multicomponent solutions was established. The affinity of the sorbent in accordance with the maximum sorption capacities increases in the following order Cu2+ > Co2+ > Ni2+ > Mn2+. High efficiency of magnesium ferrite regeneration (~100%) with aqueous solutions of magnesium chloride in the concentration range of 0.001–0.1 M was shown. The low degree of toxic metal ions desorption combined with XRD, IR spectros…

inorganic chemicals021110 strategic defence & security studiesEnvironmental EngineeringAqueous solutionMagnesiumHealth Toxicology and MutagenesisMetal ions in aqueous solutionInorganic chemistry0211 other engineering and technologieschemistry.chemical_elementSorption02 engineering and technology010501 environmental sciences01 natural sciencesPollutionIonAdsorptionchemistryDesorptionEnvironmental ChemistryLeaching (metallurgy)Waste Management and Disposal0105 earth and related environmental sciencesJournal of Hazardous Materials
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Pneumococcal histidine triads – involved not only in Zn2+, but also Ni2+ binding?

2018

Polyhistidine triad proteins, which participate in Zn2+ uptake in Streptococcus pneumoniae, contain multiple copies of the HxxHxH (histidine triad motif) sequence. We focus on three such motifs from one of the most common and well-conserved polyhistidine triad proteins, PhtA, in order to understand their bioinorganic chemistry; particular focus is given to (i) understanding which of the PhtA triads binds Zn2+ with the highest affinity (and why) and (ii) explaining whether Ni2+ (also crucial for bacterial survival and virulence) could potentially outcompete Zn2+ at its native binding site. There is no significant difference in the stability of zinc(II) complexes with the three studied protei…

inorganic chemicals0301 basic medicineChemistry030106 microbiologySignificant differenceMetals and AlloysBiophysicsVirulenceBioinorganic chemistrymedicine.disease_causeBiochemistryBiomaterials03 medical and health sciencesBiochemistryChemistry (miscellaneous)Streptococcus pneumoniaemedicineBinding siteHistidineMetallomics
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Mechanism of sulfur transfer across protein-protein interfaces: The cysteine desulfurase model system

2016

CsdA cysteine desulfurase (the sulfur donor) and the CsdE sulfur acceptor are involved in biological sulfur trafficking and in iron-sulfur cluster assembly in the model bacterium Escherichia coli. CsdA and CsdE form a stable complex through a polar interface that includes CsdA Cys328 and CsdE Cys61, the two residues known to be involved in the sulfur transfer reaction. Although mechanisms for the transfer of a sulfur moiety across protein-protein interfaces have been proposed based on the IscS-IscU and IscS-TusA structures, the flexibility of the catalytic cysteine loops involved has precluded a high resolution view of the active-site geometry and chemical environment for sulfur transfer. H…

inorganic chemicals0301 basic medicineChemistryCysteine desulfuraseInorganic chemistrychemistry.chemical_elementIsothermal titration calorimetryGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryAcceptorSulfurCatalysis0104 chemical sciences03 medical and health sciences030104 developmental biologyMoietyTransferaseBiogenesisCysteine
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Chemical and physical characterization of thermal aggregation of model proteins modulated by zinc(II) and copper(II) ions

2016

BACKGROUND: Metal ions are implicated in protein aggregation processes of several neurodegenerative pathologies, where the protein deposition occurs, and in the biotechnology field like the food technology where many processes in food manufacturing are based on thermal treatments. OBJECTIVE: The influence of Cu2+ or Zn2+ ions on the thermal aggregation process of Bovine beta-lactoglobulin (BLG) and Bovine Serum Albumin (BSA), two protein models, was studied with the aim of delineating the role of these ions in the protein aggregation kinetics and to clarify the related molecular mechanisms. METHODS: The protein structure changes were monitored by Raman spectroscopy, whereas the aggregate gr…

inorganic chemicals0301 basic medicineMetal ions in aqueous solutionKineticsInorganic chemistryBeta-lactoglobulinchemistry.chemical_elementZincProtein aggregation010402 general chemistry01 natural sciencesBovine Serum Albumin (BSA)Beta-lactoglobulin bovine serum albumin (BSA) copper and zinc ionsRaman spectroscopy dynamic light scatteringMetal03 medical and health sciencesProtein structureDynamic light scatteringcopper and zinc ionRadiology Nuclear Medicine and imagingcopper and zinc ionsBovine serum albuminBeta-lactoglobulin; Bovine Serum Albumin (BSA); copper and zinc ions; Raman spectroscopy; dynamic light scatteringbiologydigestive oral and skin physiologydynamic light scattering0104 chemical sciences030104 developmental biologychemistryvisual_artRaman spectroscopyBiophysicsbiology.proteinvisual_art.visual_art_medium
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On the Complexation of Cu(II) and Cd(II) With Polycarboxyl Ligands. Potentiometric Studies With ISE-H+, ISE-Cu2+, and ISE-Cd2+

2009

The interaction of Cu2+ and Cd2+ ions with polyacrylates (PAA, 2 kDa and 100 kDa), polymetacrylate(PMA, 5.4 kDa), and alginate (AA, 70 kDa to 100 kDa) was studied by potentiometry, using ISE-Cu2+, ISE-Cd2+, and ISE-H+ electrodes. The investigations were performed in NaNO3 aqueous solutions, in the ionic strength range 0.10 e I (mol ·L-1) e 0.75, at T ) 298.15 K. The “diprotic-like model” was used to explain the acid-base behavior of the polycarboxylates under investigation (for this model, the monomeric unit of the polyelectrolyte is considered as a dicarboxylate). The results give evidence for the formation of the ML species in all the systems investigated. In addition, the MLH species was…

inorganic chemicalsAcrylate polymerchemistry.chemical_classificationSequestering abilitypolycarboxylic acidsLigandGeneral Chemical EngineeringIonic strength dependencePotentiometric titrationInorganic chemistryGeneral ChemistryUronic acidComplexation Potentiometric study polyelectrolytesPolysaccharidePolyelectrolytechemistry.chemical_compoundchemistryIonic strengthSodium nitrateSettore CHIM/01 - Chimica Analiticapolycarboxylic acids; Sequestering ability; Ionic strength dependenceNuclear chemistryJournal of Chemical & Engineering Data
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Correlations of blood selenium with hematological parameters in West German adults.

1988

The serum selenium and the whole blood selenium of 72 healthy persons (47 women, 25 men) was determined. There exist sex specific differences of the whole blood selenium between men (98 +/- 19 micrograms Se/L) and women (89 +/- 17 micrograms Se/L). The serum selenium did not show sex specific differences, but sex specific differences are found if the total amount of extracellular selenium is calculated by correction of the serum selenium with the hematocrit. Women have more extra-cellular selenium/L whole blood (40 +/- 8 micrograms Se) than men (36 +/- 7 micrograms Se). Men have more intraerythrocyte selenium (cellular selenium = 67 +/- 14 micrograms Se) in one L whole blood than women (52 …

inorganic chemicalsAdultMalemedicine.medical_specialtyEndocrinology Diabetes and MetabolismClinical Biochemistrychemistry.chemical_elementHematocritBiochemistryInorganic ChemistryLipid peroxidationchemistry.chemical_compoundSeleniumInternal medicineMolemedicineExtracellularHumansWhole bloodchemistry.chemical_classificationSex CharacteristicsHematologic Testsmedicine.diagnostic_testGlutathione peroxidaseSpectrophotometry AtomicBiochemistry (medical)Germany Westfood and beveragesGeneral MedicineEndocrinologychemistryFemaleHemoglobinSeleniumBiological trace element research
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Total oxidation of propane in vanadia-promoted platinum-alumina catalysts: Influence of the order of impregnation

2015

Differently prepared vanadium promoted Pt/alumina catalysts have been prepared, characterized and tested for propane total oxidation. V-promoted Pt/Al2O3 catalysts have shown remarkably higher catalytic activity than V-free Pt/Al2O3 catalyst. Among V-promoted Pt catalysts that prepared by coimpregnation gave the highest alkane conversions in the whole range of reaction temperatures studied. Factors such as Pt particle size or the oxidation state of platinum do not seem to be the responsible for the enhanced performance. Modification of the redox properties of the catalyst (i.e. high reducibility of vanadium species) likely provoked by the close contact between platinum particles and vanadiu…

inorganic chemicalsAlkanechemistry.chemical_classificationorganic chemicalsInorganic chemistrychemistry.chemical_elementVanadiumGeneral ChemistryRedoxCatalysisCatalysischemistry.chemical_compoundchemistryOxidation statePropaneParticle sizePlatinumCatalysis Today
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