Search results for "calor"

showing 10 items of 866 documents

α,β-Poly(N-Hydroxyethyl)-DL-Aspartamide Hydrogels as Drug Delivery Devices

1996

α,β-poly(N-hydroxyethyl)-DL-aspartamide (PHEA) was exposed to gamma radiation to obtain micromatrices able to swell in an aqueous medium. Crosslinked PHEA was loaded with an anti-inflammatory drug, 4-biphenylacetic acid (BPAA) and the drug dispersion in the network was investigated by X-ray analysis. The BPAA loaded PHEA microparticles were also characterized by dimensional analysis, which showed the presence of quasispherical shapes. The drug release from PHEA hydrogel was studied in vitro in a pH 1.1 (simulated gastric juice) and in a pH 7.4 buffer solution, respectively. The experimental data indicate that an anomalous delivery occurs, but Fickian diffusion through swollen PHEA hydrogel…

chemistry.chemical_classificationLiposomePolymers and PlasticsChemistryStereochemistry0206 medical engineeringtechnology industry and agricultureBiomaterialBioengineeringBiological membrane02 engineering and technologyPolymerBuffer solution021001 nanoscience & nanotechnology020601 biomedical engineeringBiomaterialschemistry.chemical_compoundDifferential scanning calorimetrySelf-healing hydrogelsDrug deliveryMaterials Chemistry0210 nano-technologyNuclear chemistryJournal of Bioactive and Compatible Polymers
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2020

Tristriazolotriazines (TTTs) with a threefold alkoxyphenyl substitution were prepared and studied by DSC, polarized optical microscopy (POM) and X-ray scattering. Six pentyloxy chains are sufficient to induce liquid-crystalline behavior in these star-shaped compounds. Thermotropic properties of TTTs with varying substitution patterns and a periphery of linear chains of different lengths, branching in the chain and swallow-tails, are compared. Generally, these disks display broad and stable thermotropic mesophases, with the tangential TTT being superior to the radial isomer. The structure–property relationships of the number of alkyl chains, their position, length and structure were studied.

chemistry.chemical_classificationMaterials science010405 organic chemistryScatteringDiscotic liquid crystalOrganic ChemistryPharmaceutical Science010402 general chemistryBranching (polymer chemistry)01 natural sciencesThermotropic crystal0104 chemical sciencesAnalytical ChemistryCrystallographyDifferential scanning calorimetrychemistryChemistry (miscellaneous)Drug DiscoveryX-ray crystallographyAlkoxy groupMolecular MedicinePhysical and Theoretical ChemistryAlkylMolecules
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Synthesis and phase behaviour of liquid-crystalline side group polyesters

1990

Abstract Several series of liquid-crystalline side group polymers with a polyester backbone structure have been synthesized using mesogenic diethylmalonate and 1,3-propanediol derivatives. The structures of the polymer backbone and the mesogenic units have been varied systematically. As shown by differential scanning calorimetry, polarizing microscopy and X-ray diffraction, the side group polyesters exhibit nematic and/or smectic mesophases. Polyesters synthesized from mesogenic diethylmalonate derivatives can tolerate long non-mesogenic segments in the polymer main chain without losing their liquid crystal properties. X-ray studies suggest that some of the smectic polymers exhibit interdig…

chemistry.chemical_classificationMaterials scienceBilayerMesogenGeneral ChemistryPolymerCondensed Matter PhysicsPolyesterCrystallographyDifferential scanning calorimetrychemistryLiquid crystalPhase (matter)Organic chemistryGeneral Materials SciencePendant groupLiquid Crystals
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Detection of the liquid ? liquid demixing by differential scanning calorimetry

1983

From theoretical considerations it is concluded that the demixing temperatures of moderately concentrated polymer solutions should manifest themselves in a change of the slope of the corresponding DSC trace; the effects are expected to suffice for detection by means of the commercially available dual furnace instrument DSC-2C from Perkin-Elmer.

chemistry.chemical_classificationMaterials scienceChromatographyPolymers and PlasticsAnalytical chemistryGeneral ChemistryPolymerCondensed Matter PhysicsDifferential scanning calorimetrychemistryMaterials ChemistryLiquid liquidChemical solutionPhase diagramPolymer Bulletin
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Aggregation in aqueous media of tri-block copolymers tuned by the molecular selectivity of cyclodextrins

2009

The water + cyclodextrin + poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) mixtures have been investigated to explore the temperature effect on the aggregation of the copolymer in the presence of cyclodextrins (CDs). The CDs with different cavity sizes were chosen because they may include either the hydrophilic poly(ethylene oxides) block or both kinds of blocks. The differential scanning calorimetry and viscosity experiments straightforwardly evidenced that the critical micellar temperature is shifted to larger values by adding a CD which is able to include the middle poly(propylene oxide) block while it is not influenced by the presence of CD which is selective to the poly…

chemistry.chemical_classificationMaterials scienceEthyleneEthylene oxideCyclodextrincopolymer cyclodextrins supramolecular aggregates thermodynamicCondensed Matter PhysicsInclusion compoundchemistry.chemical_compoundDifferential scanning calorimetrychemistryPolymer chemistryCopolymerPropylene oxidePhysical and Theoretical ChemistrySelectivitySettore CHIM/02 - Chimica Fisica
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Laponite clay in homopolymer and tri-block copolymer matrices

2007

Macromolecule/laponite nanomaterials were studied by DSC and X-ray diffraction techniques. The matrices are poly(ethylene) glycols at various molecular masses and poly(ethylene oxides)-poly(propylene oxides)-poly(ethylene oxides) tri-block copolymers. The latter were tuned by modulating the molecular masses, at constant hydrophilic/hydrophobic ratio, and the hydrophilicity. For all the investigated systems, the enthalpy of melting (ΔH m) is nearly constant up to a given composition thereafter it increases monotonically reaching the value of the pure macromolecule. We proposed a model to interpret the DSC data. Briefly, it was invoked a mechanism of interaction following which some segments …

chemistry.chemical_classificationMaterials scienceIntercalation (chemistry)EnthalpyPolymerCondensed Matter Physicsdispersion in polymer matrices DSC laponite poly(ethylene)glycols poly(ethylene oxide)poly(propylene oxide)poly(ethylene oxide) X-ray diffractionDifferential scanning calorimetrychemistryChemical engineeringPolymer chemistryX-ray crystallographyCopolymerPhysical and Theoretical ChemistryThermal analysisMacromoleculeJournal of Thermal Analysis and Calorimetry
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Synthesis and thermal behavior of Janus dendrimers, part 2

2010

Abstract The thermal properties of twelve Janus-type dendrimers up to the second generation were evaluated by termogravimetric analysis (TGA) and differential scanning calorimetry (DSC). Compounds consist of the dendritic bisMPA based polyester moieties, and either 3,4-bis-dodecyloxybenzoic acid, 3,5-bis-dodecyloxybenzoic acid or 3,4,5-tris-dodecyloxybenzoic acid moieties, attached to opposite sides of the pentaerythritol core. The thermal stability of the compounds was evaluated by TGA, displaying onset decomposition temperatures ( T d ) at around 250 °C. DSC measurements upon heating and cooling confirmed that OH terminated Janus dendrimers featuring large polarity difference in opposite …

chemistry.chemical_classificationMaterials scienceMesophaseCondensed Matter PhysicsPentaerythritolThermogravimetryCrystallographychemistry.chemical_compoundDifferential scanning calorimetrychemistryDendrimerThermal stabilityPhysical and Theoretical ChemistryThermal analysisInstrumentationAlkylThermochimica Acta
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Transparent thermoplastic polyurethanes based on aliphatic diisocyanates and polycarbonate diol

2016

Segmented thermoplastic polyurethanes (PUs) were synthetized using polycarbonate diol as soft segment with a molar mass of 500 and as a hard segment 1,5-pentanediol with a combination of isophorone diisocyanate (IPDI) and hexamethylene diisocyanate (HDI). Differential scanning calorimetry, differential mechanical analysis, Fourier transform infrared-attenuated total reflection spectroscopy, haze, transmittance, hardness, tensile properties and retention of tensile properties tests were employed to characterize the different PUs. The results of this study show that IPDI/HDI relation has a significant impact on the phase mixing, crystallinity and therefore on the PU’s properties. The variati…

chemistry.chemical_classificationMaterials scienceMolar massThermoplasticPolymers and PlasticsDiol02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistry.chemical_compoundCrystallinityDifferential scanning calorimetrychemistryvisual_artMaterials Chemistryvisual_art.visual_art_mediumHexamethylene diisocyanateComposite materialPolycarbonateIsophorone diisocyanate0210 nano-technologyJournal of Elastomers & Plastics
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Polyethylene glycol/clay nanotubes composites

2012

Nanocomposites of poly(ethylene) glycol (PEG) 20000 filled with clay nanotubes (HNTs) were prepared. The thermal properties obtained from thermogravimetry and differential scanning calorimetry were correlated to the morphology imaged by scanning electron microscopy. Low amounts of HNTs generate compact structure while large amounts of HNTs create craters and voids. The decrease of polymer degradation temperature in the presence of large amount of nanoclay (ca. 80 wt%) is a consequence of the morphology at the mesoscale range. The thermal opposite effect observed in the HNTs low regime (up to ca. 20 wt%) is due to the gas entrapment into the nanoparticles lumen. The quantitative analysis of …

chemistry.chemical_classificationMaterials scienceNanocompositeNanoparticlePolymerPolymer adsorptionPolyethylene glycolCondensed Matter PhysicsNanotube polymerThermogravimetrychemistry.chemical_compoundDifferential scanning calorimetryPolymer degradationchemistryPhysical and Theoretical ChemistryComposite materialSettore CHIM/02 - Chimica FisicaJournal of Thermal Analysis and Calorimetry
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Methylcellulose-Based Edible Films and Coatings:  2. Mechanical and Thermal Properties as a Function of Plasticizer Content

1997

Several edible films based on methylcellulose and polyethylene glycol 400 (PEG400) were prepared and stored until equilibration at different relative humidities. Tensile stress−strain curves show very different behaviors as a function of PEG400 and relative humidity. Tensile strength strongly depends on relative humidity and then on water content, more than on PEG400 content. On the contrary, elongation is dependent both on water and PEG400. These differences correspond to the glass transition of the polymer, which affects the elongation more than the tensile strength. However, from DSC measurements, it appears that the PEG400 has no or a very low compatibility with the methylcellulose matr…

chemistry.chemical_classificationMaterials sciencePlasticizerGeneral ChemistryPolymerPolyethylene glycolchemistry.chemical_compoundDifferential scanning calorimetrychemistryPolymer chemistryUltimate tensile strengthRelative humidityElongationComposite materialGeneral Agricultural and Biological SciencesGlass transitionJournal of Agricultural and Food Chemistry
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