Search results for " Modification"

showing 10 items of 781 documents

Isotropic stochastic flow of homeomorphisms on Sd for the critical Sobolev exponent

2006

Abstract In this work, we shall deal with the critical Sobolev isotropic Brownian flows on the sphere S d . Based on previous works by O. Raimond and LeJan and Raimond (see [O. Raimond, Ann. Inst. H. Poincare 35 (1999) 313–354] and [Y. LeJan, O. Raimond, Ann. of Prob. 30 (2002) 826–873], we prove that the associated flows are flows of homeomorphisms.

Sobolev exponentKolmogoroff modification theoremApplied MathematicsGeneral MathematicsEigenvectorIsotropyMathematical analysisSpherical representationHomeomorphismNon-Lipschitzian conditionSobolev spacesymbols.namesakeLaplace operatorMathematics::ProbabilityPoincaré conjecturesymbolsExponentIsotropic flowsLaplace operatorCritical exponentBrownian motionMathematicsJournal de Mathématiques Pures et Appliquées
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N6 -Methyladenosine Modification in Chronic Stress Response Due to Social Hierarchy Positioning of Mice

2021

Appropriately responding to stressful events is essential for maintaining health and well-being of any organism. Concerning social stress, the response is not always as straightforward as reacting to physical stressors, e.g., extreme heat, and thus has to be balanced subtly. Particularly, regulatory mechanisms contributing to gaining resilience in the face of mild social stress are not fully deciphered yet. We employed an intrinsic social hierarchy stress paradigm in mice of both sexes to identify critical factors for potential coping strategies. While global transcriptomic changes could not be observed in male mice, several genes previously reported to be involved in synaptic plasticity, l…

Social stressMethyltransferase complexbehaviorQH301-705.5sex differenceStressorCell BiologyBiologydominancechemistry.chemical_compoundtranscriptomicschemistryCorticosteroneepigenetic modificationSynaptic plasticityChronic stressmethyltransferaseMRNA methylationN6-MethyladenosineBiology (General)NeuroscienceDevelopmental BiologyFrontiers in Cell and Developmental Biology
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Halloysite nanotubes as nanoreactors for heterogeneous micellar catalysis

2021

Abstract Hypothesis Electrostatic attractions between the anionic head group of sodium alkylsulphates and the positively charged inner surface of halloysite nanotubes (HNTs) drive to the formation of tubular inorganic micelles, which might be employed as nanoreactors for the confinement of non polar compounds in aqueous media. On this basis, sodium alkylsulphates/halloysite hybrids could be efficient nanocatalysts for organic reactions occurring in water. Experiments Sodium decylsulphate (NaDeS) and sodium dodecylsulphate (NaDS) were selected for the functionalization of the halloysite cavity. The composition, the structure and the surface charge properties of the hybrid nanotubes were dete…

SodiumMicellar catalysischemistry.chemical_elementNanoreactorengineering.materialHalloysiteMicelleCatalysisBiomaterialsMicroviscosityColloid and Surface ChemistryPulmonary surfactantNanotechnologyMicellesNanotubesChemistryHalloysite nanotubesSodium alkylsulphatesNanomaterial-based catalystSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsInorganic micellesChemical engineeringengineeringSurface modificationClay
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Different Type Clay Amendments for Lead Immobilization in Contaminated Soils

2014

Contamination with lead in soil is a crucial problem in industrial and military sites. Immobilization of lead by natural and modified clay as soil amendment can be an effective solution to this problem. Quaternary and Devonian clays were chosen for modification with NaCl, CaCl2, FeOOH and Ca10(PO4)6(OH)2 in different proportions of Ca/P equimolar ratio to test and compare immobilization efficiency of lead (II) on raw and modified clays by using a batch leaching test. The aim of the study is to compare different types of raw and modified clays as soil amendments by lead immobilization properties.

Soil conditionerContaminated soilsMaterials scienceIron oxyhydroxideEnvironmental chemistryClay modification hydroxyapatite immobilization iron oxyhydroxide soil amendmentsAmendmentSoil scienceLeaching (metallurgy)ContaminationEffective solutionMaterial Science and Applied Chemistry
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ChemInform Abstract: Photochemical Functionalization of Allyl Benzoates by C-H Insertion.

2013

The photoreactivity of allyl benzoates, containing an electron-rich double bond, has been explored by irradiation at 305 nm in different solvents. Solvent addition products arising from an insertion of the alpha H–C bonds of THF, dioxane, and i-PrOH to the allylic double bond was realized. The observed reactivity depended on reaction conditions and substitution pattern of the substrate. A DFT study on this unusual reaction was performed allowing the formulation of two mechanistic pathways.

SolventReaction conditionschemistry.chemical_classificationAllylic rearrangementDouble bondchemistrySubstrate (chemistry)Surface modificationReactivity (chemistry)General MedicinePhotochemistryBenzoatesChemInform
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Utilisation of barium-modified analcime in sulphate removal: Isotherms, kinetics and thermodynamics studies

2017

Abstract Analcime and commercial zeolite were employed as a precursor for preparing sorbent material for SO42− removal over barium modification. Three sorbents were prepared: barium-modified analcime (ANA-Na-Ba), barium-modified acid-washed analcime (ANA-Ac-Na-Ba) and barium-modified zeolite (ZSM5-Na-Ba). Of the prepared materials, ANA-Ac-Na-Ba was the most efficient sorbent material for SO42− removal, with a maximum sorption uptake of 13.7 mg g−1 at room temperature. Batch sorption experiments were performed to evaluate the effect of initial pH, initial SO42− concentration, sorbent dosage, temperature and contact time of sorption. Several isotherms were applied to describe the experimental…

SorbentAnalcimeProcess Chemistry and TechnologyKineticsInorganic chemistryChemical modificationchemistry.chemical_elementBariumSorption02 engineering and technology010501 environmental sciencesengineering.material021001 nanoscience & nanotechnology01 natural sciencesAdsorptionchemistryChemical engineeringengineering0210 nano-technologySafety Risk Reliability and QualityZeoliteWaste Management and Disposal0105 earth and related environmental sciencesBiotechnologyJournal of Water Process Engineering
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Reactive surface coatings based on polysilsesquioxanes: universal method toward light-responsive surfaces.

2011

Reactive surface coatings were used as an ideal precursor coating for the fabrication of three different photoswitchable surface coatings in parallel. Different light-responsive moieties, such as azobenzene, salicylideneaniline, and spiropyran, were immobilized on glass, polycarbonate, and steel surfaces. Independent from the underlying substrate, wettability could be switched reversibly by UV irradiation. The maximum switching range was obtained after functionalization of the reactive coating with spiropyran, resulting in a contact angle difference between the two isomeric states of almost 30°.

SpiropyranMaterials scienceSubstrate (electronics)engineering.materialPhotochemistryContact anglechemistry.chemical_compoundCoatingAzobenzenechemistryvisual_artengineeringvisual_art.visual_art_mediumSurface modificationGeneral Materials ScienceWettingPolycarbonateACS applied materialsinterfaces
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ChemInform Abstract: Synthesis and Functionalization of Chalcogenide Nanotubes

2011

New synthetic approaches to MS 2 (M = Sn, Nb, Mo, W) chalcogenide nanostructures are highlighted. Most chalcogenide particles can be functionalized directly with inorganic nanoparticles such as Au, ZnO or MnO. Depending on the Pearson hardness of the metal involved, the functionalization may be reversible or irreversible. A covalent functionalization strategy is based on a steric shielding of the coordination sphere of transition metal atoms in such a way that only coordination sites are available for bonding to the chalcogenide surface. This allows the immobilization of fluorophors, redox active groups or proteins onto chalcogenide nanoparticle.

Steric effectsNanostructureCoordination sphereChalcogenideNanoparticleGeneral MedicineMetalChalcogenchemistry.chemical_compoundchemistryChemical engineeringvisual_artvisual_art.visual_art_mediumSurface modificationChemInform
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DFT studies of COOH tip-functionalized zigzag and armchair single wall carbon nanotubes

2011

Structure and energy calculations of pristine and COOH-modified model single wall carbon nanotubes (SWCNTs) of different length were performed at B3LYP/6-31G* level of theory. From 1 to 9 COOH groups were added at the end of the nanotube. The differences in structure and energetics of partially and fully functionalized SWCNTs at one end of the nanotube are observed. Up to nine COOH groups could be added at one end of (9,0) zigzag SWCNT in case of full functionalization. However, for (5,5) armchair SWCNT, the full functionalization was impossible due to steric crowding and rim deformation. The dependence of substituent attachment energy on the number of substituents at the carbon nanotube ri…

Steric effectsNanotubeMaterials scienceBiomedicine generalCarboxylic AcidsSubstituentHealth InformaticsCarbon nanotubeDFTCatalysislaw.inventionEnd-substitutionInorganic Chemistrychemistry.chemical_compoundCarboxylation energylawOrganic chemistryComputer SimulationComputer Applications in ChemistryPhysical and Theoretical ChemistryAnthracenesLife Sciences generalOriginal PaperNanotubes CarbonOrganic ChemistryZigzag and armchair SWCNTBenzoic AcidPhenanthrenesComputer Science ApplicationsChemistryCrystallographyModels ChemicalComputational Theory and MathematicschemistryZigzagComputer Appl. in Life SciencesQuantum TheoryThermodynamicsMolecular MedicineSurface modificationCOOH functionalization
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Synthesis and functionalization of chalcogenide nanotubes

2010

New synthetic approaches to MS 2 (M = Sn, Nb, Mo, W) chalcogenide nanostructures are highlighted. Most chalcogenide particles can be functionalized directly with inorganic nanoparticles such as Au, ZnO or MnO. Depending on the Pearson hardness of the metal involved, the functionalization may be reversible or irreversible. A covalent functionalization strategy is based on a steric shielding of the coordination sphere of transition metal atoms in such a way that only coordination sites are available for bonding to the chalcogenide surface. This allows the immobilization of fluorophors, redox active groups or proteins onto chalcogenide nanoparticle.

Steric effectsNanotubeMaterials scienceNanostructureCoordination sphereChalcogenideNanoparticleNanotechnologyCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsMetalchemistry.chemical_compoundChemical engineeringchemistryvisual_artvisual_art.visual_art_mediumSurface modificationphysica status solidi (b)
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