Search results for "solvent"

showing 10 items of 1395 documents

Viscosity of Polymer Solutions over the Full Range of Composition: A Thermodynamically Inspired Two-Parameter Approach

2015

The approach yields the following relation for the relative viscosity η rel as a function of polymer concentration c (mass/volume): ln ηrel = c/(1 + pc + qc2). Reduced concentrations c (defined as c = c[η], where [η] is the intrinsic viscosity) are used instead of c to incorporate thermodynamic information. The parameters p and q account for changes in the free volume of the solvent caused by the polymer. The analysis of literature data for seven very dissimilar systems discloses the following common feature: p > 0 and q < 0. This means that the curves in the plots of ln ηrel as a function of c are normally located below the tangent at low c and above it at high c. The values of p and q cor…

chemistry.chemical_classificationChemistryGeneral Chemical EngineeringIntrinsic viscosityRelative viscosityThermodynamicsTangentGeneral ChemistryFunction (mathematics)PolymerIndustrial and Manufacturing EngineeringSolventViscosityVolume (thermodynamics)Industrial &amp; Engineering Chemistry Research
researchProduct

Role of residual water hydrogen bonding in sugar/water/biomolecule systems: a possible explanation fortrehalose peculiarity

2007

We report on the set of experimental and simulative evidences which enabled us to suggest how biological structures embedded in a non-liquid water–saccharide solvent are anchored to the surrounding matrix via a hydrogen bond network. Such a network, whose rigidity increases by decreasing the sample water content, couples the degrees of freedom of the biostructure to those of the matrix and gives place to protein–saccharide–water structures (protein–solvent conformational substates). In particular, the whole set of data evidences that, while the protein–sugar interaction is well described in terms of a water entrapment hypothesis, the water replacement hypothesis better describes the sugar–m…

chemistry.chemical_classificationChemistryHydrogen bondStereochemistryBiomoleculeCondensed Matter PhysicsTrehaloseSolventchemistry.chemical_compoundtrehalose water FTIR spectroscopyRigidity (electromagnetism)MembraneChemical physicsMoleculeGeneral Materials ScienceSupercoolingJournal of Physics: Condensed Matter
researchProduct

Organo-phosphorus compounds—LXVI

1970

Abstract The recemization kinetics of (+)-methyl-n-propylphenylphosphine were studied in several solvents of widely varying polarity. The recemization followed first order kinetics in every solvent with approximately equal activation energies of 30 ±3 kcal/mole. The rate of racemization showed no dependence on solvent polarity and could not be correlated with any known solvent parameters. The unusually slow racemization in caproic acid and in tributyl borate were attributed to partial salt and adduct formation respectively.

chemistry.chemical_classificationChemistryPhosphorusOrganic ChemistryInorganic chemistryKineticsSalt (chemistry)chemistry.chemical_elementBiochemistryCaproic AcidAdductSolventDrug DiscoveryBoronRacemizationTetrahedron
researchProduct

Thermodynamics of copolymer solutions: how the pair interactions contribute to the overall effect.

2014

Vapor pressure measurements were performed for solutions of poly(methyl methacrylate-ran-tert-butyl methacrylate) with different weight fractions of tert-butyl methacrylate units, and their parental homopolymers in chloroform at 323 K, over a large domain of concentrations. The Flory–Huggins interaction parameters obtained from these experimental investigations show complex dependences of the Flory–Huggins interaction parameter on concentration and copolymer composition. This behavior can be modeled by taking into account an approach which considers the ability of the polymers to rearrange in a response to changes in their molecular surroundings [Adv. Polym. Sci. 2011, 238, 1–66]. According…

chemistry.chemical_classificationChloroformMaterials scienceVapor pressureThermodynamicsPolymerFlory–Huggins solution theoryMethacrylateSurfaces Coatings and FilmsSolventchemistry.chemical_compoundchemistryMaterials ChemistryCopolymerPhysical and Theoretical ChemistryMixing (physics)The journal of physical chemistry. B
researchProduct

Evaluating the potential of cell disruption technologies for green selective extraction of antioxidant compounds from Stevia rebaudiana Bertoni leaves

2015

Abstract An increased interest has been shown by both food technologists and food industry regarding Stevia rebaudiana Bertoni leaves ( Stevia ) for their high content of bioactive components (phenolic compounds, vitamin C, carotenoids). The aim of this work was to study the effect of emerging technologies such as high voltage electrical discharges (HVED) and pulsed electric fields (PEF) and ultrasounds (US) on the intensification of the extraction of valuable compounds from Stevia leaves. The proposed processes combined pretreatment (HVED, PEF and US) and extraction of intracellular compounds using water as solvent at ambient temperature. The energy inputs of the treatments varied from 24 …

chemistry.chemical_classificationChlorophyll aAntioxidantChromatographyFood industryChemistrybusiness.industryDPPHmedicine.medical_treatmentExtraction (chemistry)Solventchemistry.chemical_compoundStevia rebaudianamedicinebusinessCarotenoidFood ScienceJournal of Food Engineering
researchProduct

Modelling retention and peak shape of small polar solutes analysed by nano-HPLC using methacrylate-based monolithic columns.

2019

Abstract The development of methacrylate-based monolithic columns was studied for the separation of pharmaceutical hydrophilic compounds in nano-liquid chromatography. The selected polymerisation mixture consisted of 7.5% hexyl methacrylate, 4.5% methacrylic acid and 18.0% ethylene dimethacrylate (w/w), in a binary porogenic solvent (35:35 w/w 1-propanol/1,4-butanediol). The polymer synthesised with this mixture has a good permeability, not excessive back-pressure, and reasonable retention times for polar and non-polar solutes. Monolithic columns (12 cm total capillary length, 100 μm i.d.), prepared with this mixture, were able to produce hydrogen bonding and electrostatic interactions, giv…

chemistry.chemical_classificationChromatography010401 analytical chemistry02 engineering and technologyPolymer021001 nanoscience & nanotechnologyMethacrylate01 natural sciencesBiochemistryHigh-performance liquid chromatography0104 chemical sciencesAnalytical ChemistrySolventchemistry.chemical_compoundchemistryMethacrylic acidEnvironmental ChemistryAlkylbenzenesParticle size0210 nano-technologySelectivitySpectroscopyAnalytica chimica acta
researchProduct

Supercritical Assisted Atomization: Polyvinylpyrrolidone as Carrier for Drugs with Poor Solubility in Water

2013

Supercritical assisted atomization (SAA) is an efficient technique to produce microparticles and composite microspheres formed by polymers and pharmaceutical compounds. In this work polyvinylpyrrolidone (PVP) was proposed as carrier for pharmaceutical compounds that show a poor solubility in water medium. Indeed, this polymer is hydrosoluble and can be generally used to enhance the dissolution rate of hydrophobic compounds when finely dispersed in it. However, it is difficult to obtain coprecipitates with a uniform dispersion of the active molecule using other micronization techniques. The experiments were performed using ethanol as solvent; SAA plant was operated at 40°C and 76 bar in the …

chemistry.chemical_classificationChromatographyArticle SubjectPolyvinylpyrrolidoneSettore ING-IND/25 - Impianti ChimiciGeneral ChemistryPolymerSupercritical fluidlcsh:ChemistrySolventSupercritical fluids atomization drug particleslcsh:QD1-999chemistryChemical engineeringmedicineSolubilityMicronizationDispersion (chemistry)Dissolutionmedicine.drug
researchProduct

Size‐Exclusion Chromatography in Single and Mixed Eluents: Effects of Sorption of Solvent and Polymer Solutes on Novel TSK‐Gel Super AW Columns

2005

Abstract The novel TSK Gel Super AW column packing is based on a polymeric gel with residual hydrophobic and hydrophilic groups on the gel surface. These groups can act as active sites making the chromatographic support compatible both with polar and apolar eluents. This interesting property allows the elution of systems of very different polarities but also induces binary polymer–gel, polymer–solvent, and solvent–gel enthalpic interactions that lead to a mixture of separation mechanisms: repulsion, partition, or adsorption besides the main size‐exclusion chromatography (SEC) mechanism. For this reason, the elution behaviour of many and diverse polymer/solvent systems has been studied in th…

chemistry.chemical_classificationChromatographyChemistryElutionClinical BiochemistrySize-exclusion chromatographyPharmaceutical ScienceSorptionPolymerBiochemistryAnalytical ChemistrySolventGel permeation chromatographyAdsorptionMolar mass distributionJournal of Liquid Chromatography &amp; Related Technologies
researchProduct

Application of Imprinted Synthetic Polymers in Binding Assay Development

2000

The first part of the review describes a method for the synthesis of molecularly imprinted polymers for use in binding assays. The method considers the many factors involved that affect the recognition properties of the materials and describes an approach to screening and optimization of these factors. The second part describes the development of binding assays using such polymers. This includes the use of different labels, the effect of solvent and buffer, the scale of the assay (amount of solid polymer), and how these influence the quality of the assay in terms of sensitivity, selectivity, and speed of analysis.

chemistry.chemical_classificationChromatographyChromatographyPolymersLigand binding assayDrug Evaluation PreclinicalMolecular ConformationMolecularly imprinted polymerPolymerBuffersLigandsSensitivity and SpecificityGeneral Biochemistry Genetics and Molecular BiologyPharmaceutical PreparationschemistrySolventsAdsorptionSelectivityMolecular BiologyMethods
researchProduct

Chiral separation of ephedrines by liquid chromatography using β-cyclodextrins

2001

β-cyclodextrins (β-CDs) have been evaluated as chiral recognition agents for the enantioseparation of ephedrines by liquid chromatography (LC). The compounds tested were norephedrine, ephedrine, pseudoephedrine, N-methylephedrine and N-methylpseuoephedrine. Two possibilities have been investigated, the employment of a chiral stationary phase consisting of immobilized β-cyclodextrin, and the addition of the chiral selector to the mobile phase. In the latter approach the following chiral agents have been assayed, native β-cyclodextrin (β-CD), methyl-β-cyclodextrin (M-β-CD), carboxyethyl-β-cyclodextrin (CE-β-CD), carboxymethyl-β-cyclodextrin (CM-β-CD) and hydroxypropyl-β-cyclodextrin (HP-β-CD)…

chemistry.chemical_classificationChromatographyCyclodextrinBiochemistryAnalytical ChemistryNasal decongestantChiral column chromatographySolventchemistryIonic strengthmedicineEnvironmental ChemistryEphedrineEnantiomerChiral derivatizing agentSpectroscopymedicine.drugAnalytica Chimica Acta
researchProduct