Search results for "Charge"

showing 10 items of 4686 documents

Counterion-mediated attraction and kinks on loops of semiflexible polyelectrolyte bundles.

2006

The formation of kinks in a loop of bundled polyelectrolyte filaments is analyzed in terms of the thermal fluctuations of charge density due to polyvalent counterions adsorbed on the polyelectrolyte filaments. It is found that the counterion-mediated attraction energy of filaments depends on their bending. By consideration of curvature elasticity energy and counterion-mediated attraction between polyelectrolyte filaments, the characteristic width of the kink and the number of kinks per loop is found to be in reasonable agreement with existing experimental data for rings of bundled actin filaments.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceCondensed matter physicsMolecular ConformationGeneral Physics and AstronomyThermal fluctuationsCharge densityBendingCurvatureAttractionPolyelectrolyteActinsQuantitative Biology::Cell BehaviorQuantitative Biology::Subcellular ProcessesCondensed Matter::Soft Condensed MatterActin CytoskeletonElectrolyteschemistryModels ChemicalChemical physicsThermodynamicsCounterionElasticity (economics)Physical review letters
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Temperature effects on counterion binding to spherical polyelectrolytes: the charge-discharge transition of lignosulfonate

1995

Abstract The effect of temperature on the effective charge numbers and diffusion coefficients of polyelectrolytes has not nobee dealth with in many studies. The present study concerns the temperature behavior of lignosulfonate. Lignosulfonate is a polydisperse polyelectrolyte whose molecules are compact spheres in aqueous solutions. One of its most remarkable properties is that is loses its charge in 0.1 M NaCl aqueous solution at about 40°C. In order to explain this charge-discharge transition, a theory for ion binding to spherical polyelectrolytes based on the relative population of two hydration states of the charged groups is presented. The water molecules adjacent to the charged groups…

chemistry.chemical_classificationQuantitative Biology::Biomoleculeseducation.field_of_studyGlobular proteinInorganic chemistryPopulationBiophysicsCharge numberElectrolyteIon-associationEffective nuclear chargePolyelectrolyteCondensed Matter::Soft Condensed MatterIon bindingchemistryChemical physicsElectrochemistryPhysical and Theoretical ChemistryeducationBioelectrochemistry and Bioenergetics
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Consecutive Selective Adsorption of Pentamidine and Phosphate Biomolecules on a Self-Assembled Layer:  Reversible Formation of a Chemically Selective…

1996

In situ ellipsometric film thickness measurements, FT-IR external reflectance spectroscopy, and potentiometric measurements indicated that the amphiphile pentamidine (PAM), a bisbenzamidine, associated by self-assembly with a preformed self-assembled monolayer of a mercaptoalkanoic acid on gold. The structural properties of PAM and the nature of the substrate were ideal for the formation of a densely packed monolayer. This process was fully reversible, as demonstrated by changing the pH of the surrounding medium. Thus, disassembly−reassembly occurred when the pH was cycled between 8.7 and 3. The bilayer structure, featuring a positively charged amidinium surface, was subsequently used for s…

chemistry.chemical_classificationStereochemistryBilayerBiomoleculeSubstrate (chemistry)PhosphatePhotochemistryAnalytical Chemistrychemistry.chemical_compoundchemistrySelective adsorptionMonolayerAmphiphileSurface chargeAnalytical Chemistry
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Monolayers of Bolaform Amphiphiles: Influence of Alkyl Chain Length and Counterions

1994

We have prepared self-assembled monolayers of novel cationic bolaform amphiphiles on negatively charged substrates. Most of these amphiphiles form smooth, defect-free monolayers which can be used to reverse the substrate surface charge and thus allow subsequent adsorption of anionic molecules and construction of multilayers. Atomic force microscopy, surface force measurement, and surface plasmon spectroscopy were combined to probe the molecular orientation and ordering, mechanical properties, and surface electrical properties of the monolayers. In addition, the amphiphile aggregation behavior at an air-water interface was studied by surface tension measurement, and lyotropic phase behavior …

chemistry.chemical_classificationStereochemistrySurface forceSurfaces and InterfacesCondensed Matter PhysicsSurface tensionchemistryChemical physicsAmphiphileLyotropicMonolayerElectrochemistryMoleculeGeneral Materials ScienceSurface chargeSpectroscopyAlkylLangmuir
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Strontium Insertion in Methylammonium Lead Iodide: Long Charge Carrier Lifetime and High Fill-Factor Solar Cells.

2016

The addition of Sr2+ in CH3 NH3 PbI3 perovskite films enhances the charge carrier collection efficiency of solar cells leading to very high fill factors, up to 85%. The charge carrier lifetime of Sr2+ -containing perovskites is in excess of 40 μs, longer than those reported for perovskite single crystals.

chemistry.chemical_classificationStrontiumMaterials sciencebusiness.industryMechanical EngineeringInorganic chemistryIodideDopingchemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistryMechanics of MaterialsOptoelectronicsGeneral Materials ScienceFill factorCharge carrier0210 nano-technologybusinessPerovskite (structure)Advanced materials (Deerfield Beach, Fla.)
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Hydrogenation of light hydrocarbons on palladium: theoretical study of the local surface arrangements

2001

Abstract Quantum mechanical calculations at HF, MP2 and DFT levels were used to rationalise the surface effects of the hydrocarbon lateral interactions occurring on single planar metal surfaces or on different adjacent surfaces during the hydrogenation on palladium catalyst. The different values of electronic charge, found in the different atoms of palladium clusters, were suggested as a possible explanation of the non-homogeneous behaviour already inferred for catalyst surface sites having non-isotropic local arrangement.

chemistry.chemical_classificationSurface (mathematics)Chemistrychemistry.chemical_elementCondensed Matter PhysicsElementary chargeBiochemistryCatalysisMetalPlanarHydrocarbonChemical physicsvisual_artvisual_art.visual_art_mediumOrganic chemistryPhysics::Chemical PhysicsPhysical and Theoretical ChemistryQuantumPalladiumJournal of Molecular Structure: THEOCHEM
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Fundamental and practical aspects concerning the characterization of smart textiles

2017

The research aims towards a novel methodology of ZnO impregnation onto polyamide supports, in order to attain a special inorganic-organic hybrid polymer material, with increased UV-barrier attributes and high hydrophobicity. The experimental approach employed ZnO micro particles powder. Solutions with different concentrations of ZnO powder dispersed in methanol are prepared as anti-UV finishing agent and applied onto polyamide fabric. The responsive behaviour of this complex polymer network to UV irradiation, the photo protective performance and its time stability, also the hydrophobic character are assessed by different characterization techniques. The proposed method has advantages, like:…

chemistry.chemical_classificationTextileMaterials sciencePolymer networkMicro particlesbusiness.industryProduction costNanotechnologyPolymerchemistrylcsh:TA1-2040Homogeneity (physics)PolyamideSurface chargelcsh:Engineering (General). Civil engineering (General)businessMATEC Web of Conferences
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Natural organic matter export from boreal catchments (the Salaca River basin, Latvia) and its influencing factors

2012

A noteworthy increase in the organic matter concentration and export, as well as water colour, in the catchments of the Salaca River has been observed during the last decades. This study investigates factors behind this increase: the impact of climate, land use and human loading changes on the concentrations and export of the organic matter in the Salaca River/Lake Burtnieks catchments. Proportion of wetlands in the river basin, type of land use, and runoff regime can be considered as the main factors influencing the organic carbon loadings. Despite a steady overall tendency of increase, considerable oscillations of organic matter loadings influenced by the changes in the river discharge re…

chemistry.chemical_classificationTotal organic carbonHydrologygeographygeography.geographical_feature_categoryLand useDischargeDrainage basinWetlandchemistryBorealEnvironmental scienceOrganic matterSurface runoffWater Science and TechnologyHydrology Research
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Crystal structure and Hirshfeld surface analysis of (E)-3-(benzylideneamino)-5-phenylthiazolidin-2-iminium bromide

2020

The central thiazolidine ring of the title salt, C16H16N3S+center dot Br-, adopts an envelope conformation, with the C atom bearing the phenyl ring as the flap atom. In the crystal, the cations and anions are linked by N-H center dot center dot center dot Br hydrogen bonds, forming chains parallel to the b-axis direction. Hirshfeld surface analysis and two-dimensional fingerprint plots indicate that the most important contributions to the crystal packing are from H center dot center dot center dot H (46.4%), C center dot center dot center dot H/H center dot center dot center dot C (18.6%) and H center dot center dot center dot Br/Br center dot center dot center dot H (17.5%) interactions.

chemistry.chemical_classificationcrystal structureCrystallographyHydrogen bondIminiumSalt (chemistry)General ChemistryCrystal structureCondensed Matter::Mesoscopic Systems and Quantum Hall EffectCondensed Matter PhysicsRing (chemistry)Crystalchemistry.chemical_compoundCrystallographychemistryBromideQD901-999Atomcharge assisted hydrogen bondinghirshfeld surface analysisthiazolidine ringenvelope conformationGeneral Materials ScienceActa Crystallographica Section E: Crystallographic Communications
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A Novel Zeolite-Induced Population of a Planar Viologen Conformation. New Viologen Charge Transfer Complexes and Alkene/Viologen/Zeolite Arrays

2004

A rare example of a novel zeolite-induced conformational change and a mechanism for this process are suggested in order to rationalize an unexpected spontaneous intrazeolite reduction observed during preparation of a new viologen (MQ2+)-doped zeolite (NaY). In addition, the formations of six new alkene/viologen/ zeolite charge transfer (CT) arrays using NaMQY and the previously reported NaMVY are also reported. The binding constants between MQ2+ and MV2+ and 2,3-dimethyl-2-butene (TME) were determined using the Benesi-Hildebrand approach, and the stabilities of these CT complexes are compared to their intrazeolite analogue.

chemistry.chemical_classificationeducation.field_of_studyConformational changeChemistryAlkenePopulationViologenCharge (physics)Settore CHIM/06 - Chimica OrganicaPhotochemistrySurfaces Coatings and FilmsPlanarMaterials ChemistrymedicinePhysical and Theoretical ChemistryeducationZeolitemedicine.drugZeolites Binding constants Electrochromic display devices Oxygenation
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