Search results for "SULFATE"

showing 10 items of 657 documents

Tailoring the anionic function and the side chains of comb-like superplasticizers to improve their adsorption

2015

Nowadays admixtures and especially superplasticizers are unavoidable components of the concrete formulation. The high fluidizing efficiency of the comb-like superplasticizers must not overshadow their high costs. This study aims to determine the PCE structure parameters which influence their adsorption in order to enhance their resistance to sulfate competitive adsorption and thus minimize their dosage. The PCE adsorption has been studied on calcite and ettringite which are both surfaces representative of early hydrating cement. The effect of the POE side chain length and density and also of the PCE anionic function i.e. carboxylate, dicarboxylate or phosphate on the adsorption has been ana…

chemistry.chemical_classificationEttringiteMaterials scienceInorganic chemistrySuperplasticizerCharge densityBuilding and ConstructionPolymerchemistry.chemical_compoundAdsorptionchemistrySide chainGeneral Materials ScienceCarboxylateSulfateCement and Concrete Research
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Sulfated and Non-Sulfated Glycopeptide Recognition Domains of P-Selectin Glycoprotein Ligand 1 and their Binding to P- and E-Selectin

2009

Total synthesis through block glycosylation and selective chemical O-sulfation of tyrosine residues yielded the glycopeptide recognition domain A (X=SO(3) (-)) of the P-selectin glycoprotein ligand 1, in which the terminal sialic acid of the complex hexasaccharide side chain was replaced by (S)-cyclohexyl lactic acid. In binding assays the O-sulfated structure A showed high affinity towards P-selectin, the non-sulfated towards E-selectin.

chemistry.chemical_classificationGlycosylationMembrane GlycoproteinsGlycosylationSulfatesStereochemistryGlycopeptidesGeneral ChemistryLigand (biochemistry)CatalysisGlycopeptideProtein Structure TertiarySialic acidMiceP-Selectinchemistry.chemical_compoundProtein structurechemistryBiochemistryAnimalsHumansP-selectin glycoprotein ligand-1TyrosineE-SelectinGlycoproteinAngewandte Chemie International Edition
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Novel acrylamido monomers with higher hydrophilicity and improved hydrolytic stability: II. Properties of N-acryloylaminopropanol

1996

The physico-chemical properties and the electrophoretic behavior of the novel set of monomers reported by (Simo-Alfonso et al., Electrophoresis 1996, 17, 723-731) have been evaluated. Of utmost importance was the combination of high hydrophilicity and extreme hydrolytic stability, most desired properties for, any electrophoretic matrix, especially for protein fractionation. One of these monomers (N-acryloylaminopropanol, AAP) was found indeed to be extremely hydrophilic (with a partition coefficient P of only 0.10, vs. P = 0.13 for N-acryloylaminoethoxyethanol and P = 0.20 for acrylamide) and to possess excellent stability to alkaline hydrolysis. Its hydrolysis constant (0.008 L mol-1 min-1…

chemistry.chemical_classificationHydrolysis constantElectrophoresisAcrylamidesClinical BiochemistryAcrylic ResinsSodium Dodecyl SulfatePolymerDNABiochemistryAnalytical ChemistryPartition coefficientchemistry.chemical_compoundHydrolysisElectrophoresisMonomerchemistryAcrylamidePolymer chemistryIsoelectric FocusingAlkaline hydrolysisGels
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Cellulose Nanocrystals from Lignocellulosic Raw Materials, for Oxygen Barrier Coatings on Food Packaging Films

2017

Cellulose nanocrystals (CNCs) are unique, renewable top-down nano particles from which coatings with improved gas barrier properties and new functionalities can be prepared. In this paper, the potential for obtaining such high performing nanocrystals from low-cost lignocellulosic by-products or raw materials is proved by a comparison study on CNCs obtained both from cotton linters and kraft pulp, by means of the ammonium persulfate (APS) process. Morphological and chemical characterization of the nanocrystals obtained, as well as the main functional properties of the poly(ethylene terephthalate) coated films, showed quite similar characteristics and performances of CNCs obtained from pure c…

chemistry.chemical_classificationMaterials scienceMechanical EngineeringNanoparticle02 engineering and technologyGeneral ChemistryPolymerengineering.materialRaw material010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesFilm coatingchemistry.chemical_compoundchemistryChemical engineeringKraft processCoatingengineeringGeneral Materials ScienceAmmonium persulfateComposite materialCellulose0210 nano-technologyPackaging Technology and Science
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The [3,3′-Co(1,2-C2B9H11)2]– anion as a platform for new materials: synthesis of its functionalized monosubstituted derivatives incorporating synthon…

2003

[3,3′-Co(8-C5H10O-1,2-C2B9H10)(1′,2′-C2B9H11)] (2) was synthesized by reaction of the caesium salt of [Co(C2B9H11)2]− with dimethyl sulfate in the presence of sulfuric acid as catalyst and tetrahydropyrane as solvent; the zwitterionic compound (2) yielded [3,3′-Co(8-C4H4N-(CH2)5-O-1,2-C2B9H10)(1′,2′-C2B9H11)]− (6), [3,3′-Co(8-C8H6N-(CH2)5-O-1,2-C2B9H10)(1′,2′-C2B9H11)]− (7), and [3,3′-Co(8-C12H8N-(CH2)5-O-1,2-C2B9H10)(1′,2′-C2B9H11)]− (8) through the nucleophilic addition of potassium pyrrolyl, indolyl and carbazolyl, respectively. The nucleophilic addition of the same salts on [3,3′-Co(8-C4H8O2-1,2-C2B9H10)(1′,2′-C2B9H11)] (1) yielded, respectively, [3,3′-Co(8-C4H4N-(CH2)2-O-(CH2)2-O-1,2-C…

chemistry.chemical_classificationNucleophilic additionStereochemistryChemistrySynthonSalt (chemistry)Medicinal chemistryInorganic ChemistrySolventDimethyl sulfatechemistry.chemical_compoundNucleophileIntramolecular forceMoleculeDalton Transactions
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Some observations on the determination of sulfite by reduction to sulfide with sodium borohydride

1987

Abstract Sodium borohydride is studied as an agent for reducing sulfite to sulfide. Rapid reductions are attained with greater than 97% recovery in the range 700–1200 μg of S/50 ml. Sulfate is not reduced.

chemistry.chemical_classificationSodium borohydridechemistry.chemical_compoundchemistrySulfideSulfiteInorganic chemistrySulfateSpectroscopyAnalytical ChemistryMicrochemical Journal
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Determination of albendazole and ivermectin residues in cattle and poultry-derived samples from India by micellar liquid chromatography

2021

We have developed a method, based on micellar liquid chromatography, to determine albendazole and ivermectin in dairy products and biological waste from bovine, as well as edible tissues from poultry. Anthelmitics were resolved in less than 10 min using a C18 column and a mobile phase of 0.15 mol/L sodium dodecyl sulfate – 6% 1-pentanol at buffered at pH 7 with a 0.01 M phosphate salt, running under isocratic mode at 1 mL/min. Detection was by absorbance at 292 nm. Method was successfully validated following official validation guidelines, in terms of: selectivity, sensitivity, calibration range (0.0125−0.5 mg/kg to 25−50 mg/kg), linearity (r2 > 9990), trueness (86.3–105.6%), precision (<12…

chemistry.chemical_classificationbiological wasteChromatographyanthelminticmicellar liquid chromatographydairy productsfood analysisalbendazoledrug residueSalt (chemistry)PhosphateAlbendazoleivermectinAbsorbancechemistry.chemical_compoundIvermectinchemistryMicellar liquid chromatographyfood compositionmedicineAnthelminticSodium dodecyl sulfateedible tissuesFood Sciencemedicine.drugJournal of Food Composition and Analysis
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Succinate dehydrogenase functioning by a reverse redox loop mechanism and fumarate reductase in sulphate-reducing bacteria.

2006

Sulphate- or sulphur-reducing bacteria with known or draft genome sequences (Desulfovibrio vulgaris, Desulfovibrio desulfuricans G20, Desulfobacterium autotrophicum [draft], Desulfotalea psychrophila and Geobacter sulfurreducens) all contain sdhCAB or frdCAB gene clusters encoding succinate : quinone oxidoreductases. frdD or sdhD genes are missing. The presence and function of succinate dehydrogenase versus fumarate reductase was studied. Desulfovibrio desulfuricans (strain Essex 6) grew by fumarate respiration or by fumarate disproportionation, and contained fumarate reductase activity. Desulfovibrio vulgaris lacked fumarate respiration and contained succinate dehydrogenase activity. Succi…

chemistry.chemical_classificationbiologySulfatesSuccinate dehydrogenaseMolecular Sequence DataSuccinic AcidBacillus subtilisFumarate reductasebiology.organism_classificationMicrobiologySuccinate DehydrogenaseEnzymechemistryBiochemistryFumaratesMultigene Familybiology.proteinDesulfovibrioSDHDAmino Acid SequenceDesulfovibrio vulgarisGeobacter sulfurreducensOxidation-ReductionBacteriaMicrobiology (Reading, England)
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2009

Abstract. Understanding the importance of the different oxidation pathways of sulfur dioxide (SO2) to sulfate is crucial for an interpretation of the climate effects of sulfate aerosols. Sulfur isotope analysis of atmospheric aerosol is a well established tool for identifying sources of sulfur in the atmosphere and assessment of anthropogenic influence. The power of this tool is enhanced by a new ion microprobe technique that permits isotope analysis of individual aerosol particles as small as 0.5 μm diameter. With this new single particle technique, different types of primary and secondary sulfates are first identified based on their chemical composition, and then their individual isotopic…

chemistry.chemical_compoundAmmonium sulfateIsotope fractionationchemistryEnvironmental chemistrySodium sulfateKinetic fractionationchemistry.chemical_elementSulfateSea salt aerosolSulfurEquilibrium fractionationAtmospheric Chemistry and Physics Discussions
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Thermodynamics of sulfate anion binding by macrocyclic polyammonium receptors

2001

The interaction of SO42− with polyammonium cations derived from fourteen polyamines (5 polyazacycloalkanes, 2 polyazacyclophanes, 3 phenanthrolinacyclophanes, 2 dibenzenacyclophanes and 2 acyclic polyamines) in aqueous solution has been studied by means of potentiometric and microcalorimetric techniques. Only 1 : 1 receptor–anion complexes have been found in solution. Complexed species of considerable stability are formed, although the two acyclic polyamines (dimethylpentaethylenehexaamine and dimethylhexaethyleneheptaamine) and the smallest phenanthrolinacyclophane do not interact with the anion. The complexation reactions are endothermic, or almost athermic, and promoted by invariably fav…

chemistry.chemical_compoundAqueous solutionchemistryInorganic chemistryPolymer chemistryPotentiometric titrationSulfatePhosphateReceptorAnion bindingEndothermic processIon
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