Search results for "Molar"

showing 10 items of 1069 documents

Reactive blending of a functionalized polyethylene with a semiflexible liquid crystalline copolyester

1996

Reactive blends (50/50 w/w) of a low molar mass polyethylene containing free carboxylic groups (PEox) and a semiflexible liquid crystalline polyester (SBH 1 : 1 : 2, by Eniricerche) have been prepared at 240 degrees C in a Brabender mixer, in the presence of Ti(OBu)(4) catalyst, for different mixing times (15, 60, and 120 min). In order to prove the formation of a PE-g-SBH copolymer, the blends have been fractionated by successive extractions with boiling toluene and xylene. The soluble fractions and the residues have been analyzed by Fourier transform infrared (FTIR) spectroscopy, thermogravimetry (TG and DTG), differential scanning calorimetry (DSC), and scanning electron microscopy (SEM)…

Molar massPolymers and PlasticsCOMPATIBILIZATIONChemistryGeneral ChemistryPolyethyleneCopolyesterTHERMOPLASTIC COMPOSITESSurfaces Coatings and FilmsPolyesterThermogravimetrychemistry.chemical_compoundDifferential scanning calorimetryPOLYMER BLENDSSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiChemical engineeringPolymer chemistryTRANSESTERIFICATIONMaterials ChemistryMORPHOLOGYThermal stabilityFourier transform infrared spectroscopyPOLYPROPYLENEPOLYESTERS
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ALTMET Polymerization of Amino Acid-Based Monomers Targeting Controlled Drug Release

2016

Giving the imminent necessity of a new generation of biodegradable and biocompatible polymers prepared from feedstock, the synthesis of a potentially biodegradable amino acid-based copolymer by the alternating diene metathesis (ALTMET) strategy is herein presented. The reaction was tailored to minimize isomerization and deactivation of ruthenium catalysts by intramolecular coordination with the amide carbonyl group of the amino-acid-based monomer. Alternated l-lysine–phosphoester copolymers with molar masses higher than 18 000 g/mol were obtained using Hoveyda–Grubbs second-generation and Umicore M2 catalysts. The copolymer was further used to prepare nanoparticles loaded with rifampicin (u…

Molar massPolymers and PlasticsDieneOrganic Chemistrychemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesRutheniumInorganic ChemistryMiniemulsionchemistry.chemical_compoundMonomerchemistryPolymerizationAmidePolymer chemistryMaterials ChemistryCopolymer0210 nano-technologyMacromolecules
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Hyperbranched Poly(ethylene glycol) Copolymers: Absolute Values of the Molar Mass, Properties in Dilute Solution, and Hydrodynamic Homology

2015

Hyperbranched poly(ethylene glycol) copolymers were synthesized by random anionic ring-opening multibranching copolymerization of ethylene oxide with glycidol as a branching agent, leading to poly(ethylene glycol) structure with glycerol branching points. Extending the available range of molar masses by novel synthesis strategies, a limited extent of control over the degree of polymerization was achieved by variation of the solvent in this copolymerization. Generally, absolute molar mass characterization of hyperbranched polymers still represents an unresolved challenge. A series of the hyperbranched poly(ethylene glycol)-co-(glycerol) copolymers (hbPEGs) of a wide range of molar masses (14…

Molar massPolymers and PlasticsEthylene oxideIntrinsic viscosityOrganic ChemistryDispersityDegree of polymerizationBranching (polymer chemistry)Inorganic ChemistryAbsolute molar masschemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryEthylene glycolMacromolecules
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Reactive compatibilization of PA6/LDPE blends with an ethylene–acrylic acid copolymer and a low molar mass bis-oxazoline

2003

Abstract A sample of polyamide-6 (PA) was blended with low density polyethylene (LDPE) in the 80/20 wt/wt ratio, either without and with 2 phr of an ethylene–acrylic acid copolymer (EAA), Which was known to behave as a compatibilizer precursor, and the effect of the addition of small amounts (0.2 or 0.35 phr) of a fourth component, 2,2′-(1,3-phenylene)-bis(2-oxazoline) (PBO), was investigated. The reactions of PBO with EAA, PA and their blends were studied by recording as a function of time the torque applied to the blending apparatuses and by studying the solubility behavior of the products in formic acid. The PALDPE blends were prepared in a co-rotating twin screw extruder and were charac…

Molar massPolymers and PlasticsFormic acidOrganic Chemistryreactive compatibilizationchemistry.chemical_compoundLow-density polyethylenePA/LDPE blendDifferential scanning calorimetrySettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryChemical engineeringPolymer chemistryMaterials ChemistryCopolymerPolymer blendSolubilityIonomeroxazoline
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Continuous polymer fractionation of poly(methyl vinyl ether) and a new Kuhn-Mark-Houwink relation

1995

Continuous polymer fractionation (CPF) — a new large-scale method — was applied to the technical poly(methyl vinyl ether) (PVME) using toluence as solvent and petroleum ether as non-solvent. Two different devices served as fractionation apparatus, namely a column packed with glass beads and a set of mixer-settler extractors. Advantages and draw-backs of these devices are discussed. The experiments yielded numerous PVME fractions, varying in molar mass from 22 to 87 kg/mol and in molecular non-uniformity U = (M¯w/Mn) – 1 from 0,25 to 0,41 according to gel-permeation chromatography as compared with ca. U = 1,30 for the starting material. The following Kuhn-Mark-Houwink relation was establishe…

Molar massPolymers and PlasticsIntrinsic viscosityOrganic ChemistryMark–Houwink equationFractionationMethyl vinyl etherCondensed Matter PhysicsSolventchemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryPetroleum etherPhysical and Theoretical ChemistryPolymer fractionationMacromolecular Chemistry and Physics
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Phase equilibria and interfacial tension between coexisting phases for the system water/2-propanol/poly(acrylic acid)

1995

The cloud point curve, tie-lines and interfacial tensions were measured for solutions of 50 mol-% neutralized (counter-ion Na ○+ ) poly(acrylic acid) (molar mass M w = 9 700 g/mol; polydispersity index M w /M n = 2,0) in the mixed solvent water/2-propanol at 30°C. Due to the non-uniformity of the polymer, the end-points of the tie-lines are not situated on the cloud-point curve. The interfacial tension σ, determined by means of the spinning drop method, increases in sigmoidal manner with R tl , the length of the tie-line, expressed in terms of weight fractions. An evaluation of these data in a double-logarithmic plot of σ.M -0,5 versus R tl yields a critical exponent of 4,23 as compared wit…

Molar massPolymers and PlasticsOrganic ChemistryDispersityCondensed Matter PhysicsToluenePropanolSurface tensionchemistry.chemical_compoundchemistryPhase (matter)Polymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryMass fractionAcrylic acidMacromolecular Chemistry and Physics
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Apparent Molar Mass of a Polyelectrolyte in an Organic Solvent in the Low Ionic Strength Limit As Revealed by Light Scattering

2013

The apparent molar mass of a partially quaternized poly-2-vinylpyridines (degree of quaternization 4.3% < Q < 35%) in 1-propanol is measured by light scattering at low ionic strength (10–6 M < cs < 10–3 M) as a function of polyion repeat unit concentration (7 × 10–5 monomol/L < cm,p < 4 × 10–2 monomol/L). No dialysis was applied prior to measurements. The apparent molar mass under “salt-free” conditions is smaller than the true molar mass by an order of magnitude, while approaching the true value at higher ionic strength. Concomitant data on the dependence of scattering intensity on scattering wave vector show that the dilute polyelectrolyte solutions are strongly correlated. A recent theor…

Molar massPolymers and PlasticsScatteringChemistryOrganic ChemistryInorganic chemistryAnalytical chemistryApparent molar propertyLight scatteringPolyelectrolyteInorganic ChemistryAbsolute molar massIonic strengthMaterials ChemistryMolar mass distributionMacromolecules
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Characterization of lignin dissolved during alkaline pretreatment of softwood and hardwood

2015

Various alkaline pretreatments were applied to Scots pine (Pinus sylvestris) and silver/white birch (Betula pendula/pubescens) wood chips and the characterization of sulfur-free lignin dissolved was performed. The behavior of lignin during these pretreatments (alkali charge 1–8% NaOH, time 30–120 minutes, and temperature 130–150°C) was studied mainly in terms of lignin removal efficiency and molar mass distribution of dissolved lignin. The amount of lignin in pretreatment liquors increased along with an increase in the alkali charge of 0.8–4.4% and 0.6–3.4% of o.d. pine and birch wood, respectively. The most significant parameter affecting the molar mass of the dissolved lignin was shown to…

Molar massSoftwoodbiologyBetula pendula/pubescensGeneral Chemical EngineeringScots pineligninPinus sylvestrisGeneral Chemistrymolar mass distributionbiology.organism_classificationAlkali metalchemistry.chemical_compoundchemistryBetula pendulaBotanyHardwoodMolar mass distributionLigninGeneral Materials Scienceta116Alkaline pretreatmentNuclear chemistryJournal of Wood Chemistry and Technology
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1995

About 340 g of a cycloaliphatic ionene (see formula given in the introduction) were fractionated by a continuous countercurrent extraction method (CPF). The efficiency of the separation was checked by viscometry and gel permeation chromatography (GPC). Ten different fractions with number average molecular masses between 16 000 and 29 000 D were obtained and their glass transition temperatures T g determined by differential scanning calorimetry (DSC) for their bromide and tetrafluoroborate salts. No molecular weight dependence of T g was found, in contrast to recently reported results with aliphatic ionenes, where - in case of the bromide - T g increases with rising molecular weight.

Molar massTetrafluoroboratePolymers and PlasticsGeneral Chemical EngineeringAnalytical chemistryFractionationPolyelectrolyteGel permeation chromatographychemistry.chemical_compoundDifferential scanning calorimetrychemistryBromideOrganic chemistryGlass transitionActa Polymerica
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Detailed clinical, genetic and neuroimaging characterization of OFD VI syndrome.

2012

Oral-facial-digital syndrome type VI (OFD VI) is characterized by the association of malformations of the face, oral cavity and extremities, distinguished from the 12 other OFD syndromes by cerebellar and metacarpal abnormalities. Cerebellar malformations in OFD VI have been described as a molar tooth sign (MTS), thus, including OFD VI among the "Joubert syndrome related disorders" (JSRD). OFD VI diagnostic criteria have recently been suggested: MTS and one or more of the following: 1) tongue hamartoma(s) and/or additional frenula and/or upper lip notch; 2) mesoaxial polydactyly of hands or feet; 3) hypothalamic hamartoma. In order to further delineate this rare entity, we present the neuro…

Molar tooth signNeuroimagingJoubert syndromeFrameshift mutationHypothalamic hamartomaNeuroimagingGeneticsmedicineClinical geneticHumansChildMesoaxial polydactylyGenetics (clinical)Polydactylybusiness.industryBrainInfantProteinsGeneral MedicineAnatomyOrofaciodigital Syndromesmedicine.diseaseMagnetic Resonance Imagingstomatognathic diseasesChild PreschoolMutationFemalebusinessTomography X-Ray Computed
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