Search results for "Llar"

showing 10 items of 3592 documents

Momentum-dependent interfacial tension in polymer solutions

2002

A model for the interface between a concentrated and a very dilute polymer solution is studied by Monte Carlo simulations at temperatures below the Theta temperature (in bad solvent conditions). The wave-number–dependent interfacial tension γ(q) is extracted from an analysis of the capillary wave amplitudes. It is shown that γ(q) decreases monotonically with q2, while no evidence is found for the predicted increase γ(q) ∝ κq2 with a positive bending rigidity κ of the interface at large q. Consequences for the interpretations of simulations and experiments on interfacial widths are briefly discussed.

chemistry.chemical_classificationCapillary waveMaterials scienceComputer simulationMonte Carlo methodGeneral Physics and AstronomyThermodynamicsFlexural rigidityPolymerCondensed Matter::Soft Condensed MatterMomentumSurface tensionchemistryWettingEurophysics Letters (EPL)
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‘Intrinsic’ profiles and capillary waves at interfaces between coexisting phases in polymer blends

2001

Abstract Lateral fluctuations in the local position of the center of the interface between coexisting phases in unmixed polymer blends lead to a broadening of interfacial widths; comparing self-consistent field predictions for the ‘intrinsic’ profile to simulations (or experiments), this ‘capillary wave’ broadening needs consideration. This problem has been studied by extensive Monte Carlo simulations of the bond fluctuation model for symmetrical polymer mixtures, both for free interfaces (between bulk phases) and for confined interfaces (in thin films between parallel walls). While the capillary wave predictions at large length scales are confirmed, the extraction of the ‘intrinsic’ profil…

chemistry.chemical_classificationCapillary waveMaterials scienceField (physics)Monte Carlo methodAnalytical chemistrySurfaces and InterfacesPolymerCondensed Matter::Soft Condensed MatterColloid and Surface ChemistrychemistryPosition (vector)Chemical physicsPolymer blendPhysical and Theoretical ChemistryThin filmBond fluctuation modelAdvances in Colloid and Interface Science
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Interfaces between coexisting phases of polymer mixtures: Comparison between Monte Carlo simulations and theoretical predictions

1997

Large scale Monte Carlo investigations of the interface between A-rich and B-rich phases of symmetric binary (AB) polymer mixtures are presented, using the bond fluctuation model of flexible chains with NA=NB=N=32 effective monomers. The temperature range studied, 0.144<T/Tc0.759, includes both the strong and the weak segregation limit. Interfacial free energy and interfacial structure are studied, and compared to predictions based on the selfconsistent field theory. Also the broadening of the interfacial width due to capillary waves is considered, and finite size effects due to the confinement of interfaces in thin films of polymer blends are discussed.

chemistry.chemical_classificationCapillary waveMaterials sciencePolymers and PlasticsOrganic ChemistryMonte Carlo methodThermodynamicsPolymerAtmospheric temperature rangeCondensed Matter PhysicsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMonomerchemistryMaterials ChemistryField theory (psychology)Statistical physicsPolymer blendThin filmMacromolecular Symposia
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Morphology and local organization of water-containing (1R,2S)-Dodecyl(2-hydroxy-1-methyl-2-phenylethyl)dimethylammonium bromide reverse micelles disp…

2014

The structure of (1R,2S)-dodecyl(2-hydroxy-1-methyl-2-phenylethyl)dimethylammonium bromide (DMEB) reverse micelles, at various water-to-surfactant molar ratio (R-w, R-w = [water]/[DMEB]) and DMEB concentrations, has been investigated by small angle X-ray scattering (SAXS) and extended X-ray absorption fine structure spectroscopy (EXAFS). SAXS data of dry reverse micelles are consistent with a model of spherical hydrophilic core surrounded by DMEB alkyl chains whose polydispersity decreases significantly with surfactant concentration. By adding water, a sphere to cylinder transition occurs leading to a one-dimensional growth of reverse micellar cores with R-w and surfactant concentration. Th…

chemistry.chemical_classificationChiral EXAFS SAXS liquid crystalSmall-angle X-ray scatteringAnalytical chemistryGeneral Physics and AstronomyMicellechemistry.chemical_compoundCrystallographychemistryPulmonary surfactantBromideLamellar structurePhysical and Theoretical ChemistryCounterionAbsorption (chemistry)Alkyl
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Simultaneous determination of C1−C8 n-alkyl acetates and corresponding mono-, di- and trichloroacetates on glass capillary columns with programmed te…

1982

Gas chromatography of mixtures of aliphaticn-alkyl acetates (CH3−COOR), chloroacetates (CHCl2−COOR), dichloroacetates (CHCl2−COOR) and trichloroacetates (CCl3−COOR), where the alcohol chain length (R) varied between 1 and 8, has been studied on SE-30, Carbowax 20M and OV-351 glass capillary columns with programmed temperatures from 50°C at 2, 4, 6, 8 and 10°C/min. Compounds in the homologous series are eluted in the direct order from methyl ton-octyl acetate. The isomeric chloro esters are eluted on SE-30 according to their boiling points in the order: mono-, di- and trichloro isomer, whereas on polar columns di- and trichloro esters are eluted in the reverse order. The complete separation …

chemistry.chemical_classificationChromatographyCapillary actionElutionOrganic ChemistryClinical BiochemistryChloroacetatesAlcoholBiochemistryAnalytical ChemistryHomologous serieschemistry.chemical_compoundBoiling pointchemistryGas chromatographyAlkylChromatographia
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Enzyme-assisted extraction of proteins from Citrus fruits and prediction of their cultivar using protein profiles obtained by capillary gel electroph…

2017

Abstract The suitability of protein profiles established by capillary gel electrophoresis (CGE) as a tool to discriminate between 11 cultivars of Citrus (orange and tangerine) peel and pulp was evaluated in this work. Before CGE analysis, different extraction buffers (which included enzyme-assisted treatments) were compared. The best results were achieved using 5% ( v/v ) Celluclast ® 1.5 L and 5% ( v/v ) Palatase ® 20,000 L buffers for Citrus peel and pulp protein extracts, respectively. The resulting protein profiles obtained were used to construct linear discriminant analysis (LDA) models able to distinguish Citrus peel and pulp samples according to their cultivar. In both cases, all sam…

chemistry.chemical_classificationChromatographyChemistry010401 analytical chemistryfood and beveragesProtein profile04 agricultural and veterinary sciencesOrange (colour)040401 food science01 natural sciences0104 chemical sciences0404 agricultural biotechnologyEnzymeCapillary electrophoresisCultivarFood ScienceBiotechnologyFood Control
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Correlation between hydrophobicity of amino acids and retention data in reversed-phase liquid chromatography with micellar eluents

1995

Hydrophobic character is usually expressed in terms of the partition coefficient in 1-octanol-water (log PO/W). However, measurement of this coefficient is often problematic. Retention in micellar liquid chromatography is mainly due to hydrophobic interactions and can also be used as an index of hydrophobicity. A hydrophobicity scale was established with retention data foro-phthalaldehyde (OPA)-N-acetyl-L-cysteine (NAC) amino acid derivatives, using the glycine derivative as reference. Since the OPA-NAC derivatives only differ in the nature of R1 in the amino acid (R1CH(COOH)NH2), in the absence of electrostatic interactions the hydrophobic character of the substituent was responsible for r…

chemistry.chemical_classificationChromatographyChemistryOrganic ChemistryClinical BiochemistrySubstituentReversed-phase chromatographyBiochemistryAnalytical ChemistryAmino acidPartition coefficientHydrophobic effectchemistry.chemical_compoundMicellar liquid chromatographyGlycineHydrophobicity scalesChromatographia
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Chromatographic quantitation of the hydrophobicity of ionic compounds by the use of micellar mobile phases

1998

Abstract Many biologically active compounds of interest in structure–activity relationships are ionic at physiological pH. However, ionic organic compounds are only weakly or not retained in conventional RPLC which impedes the chromatographic estimation of their hydrophobicity and the development of quantitative retention–activity relationship studies. The use of micellar mobile phases allows the retention of ionic compounds. Hydrophobic and electrostatic forces govern the retention of ionic compounds in micellar liquid chromatography. In this paper three different retention models log k–log P for ionic compounds are tested (P=partition coefficient). The retention model (log k=a log P+bα+c)…

chemistry.chemical_classificationChromatographyChemistryOrganic ChemistryIonic bondingBiological activityGeneral MedicineBiochemistryMicellar electrokinetic chromatographyAnalytical ChemistryAmino acidPartition coefficientchemistry.chemical_compoundMicellar liquid chromatographyIonic compoundDerivatizationJournal of Chromatography A
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Discontinuous electrokinetic chromatography of parabens using different substituted resonances as pseudostationary phases

1999

Resorcarene derivatives, negatively charged even at moderate pH, were synthesized and employed as pseudostationary phases to achieve mobilities exceeding that of the electroosmotic flow. Under these conditions, a discontinuous electrolyte system was developed which allows the separation of four uncharged homologous 4-hydroxybenzoic esters (parabens) within a zone of resorcarene electrolyte, and the detection of these UV active compounds in a resorcarene-free zone, free from the high UV background absorbance of the resorcarenes. Resorcarenes, with differently charged functionalities (carboxylate and phosphate groups) to provide the electrophoretic mobility and with alkyl residues of differen…

chemistry.chemical_classificationChromatographyClinical BiochemistryParabensElectrolyteResorcinareneBiochemistryAnalytical ChemistryAbsorbanceElectrophoresischemistry.chemical_compoundElectrokinetic phenomenachemistryCarboxylateSelectivityAlkylChromatography Micellar Electrokinetic CapillaryElectrophoresis
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Reversed-phase liquid chromatography without organic solvent for determination of tricyclic antidepressants

2012

The chromatographic behavior of seven tricyclic antidepressants (amitryptiline, clomipramine, doxepin, imipramine, maprotiline, nortryptiline, and trimipramine) was examined with micellar mobile phases containing the nonionic surfactant Brij-35. Acetonitrile-water mixtures were also used for comparison purposes. Tricyclic antidepressants are moderately polar basic drugs, which are positively charged in the usual working pH. This gives rise to a strong association with the alkyl chains and residual ionized silanols in silica-based stationary phases, which is translated in a high consumption of organic solvent to get appropriate retention times. Brij-35 modifies the surface of the stationary …

chemistry.chemical_classificationChromatographyFiltration and SeparationReversed-phase chromatographyTrimipramineDoxepinAnalytical ChemistrychemistryMicellar liquid chromatographyPhase (matter)medicineMaprotilineAlkylTricyclicmedicine.drugJournal of Separation Science
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