Search results for "amide"

showing 10 items of 3119 documents

Mechanical Characterization of Polysaccharide/polyaminoacid Hydrogels as Potential Scaffolds for Tissue Regeneration

2011

The mechanical properties of hydrogel scaffolds based on hyaluronic acid (HA) that were chemically crosslinked with α,β-poly(N-2-hydroxyethyl)(2-aminoethylcarbamate)-D,L-aspartamide (PHEA-EDA) were investigated. Variation of these properties as a function of three different PHEA-EDA amounts used to crosslink HA has been related to the reaction efficiency evaluated using a colorimetric assay. Moreover, the amount of unreacted amino groups that was still present in the hydrogels was related to the attachment behavior of human dermal fibroblasts to the hydrogel surface. The mechanical data and biological results suggest the suitability of the investigated hydrogels as scaffolds for the regener…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsGeneral Chemical EngineeringRegeneration (biology)Organic Chemistrytechnology industry and agriculturemacromolecular substancesfibroblast attachment; hyaluronic acid; mechanical properties; polyaspartamide; scaffoldsPolysaccharidePolymer engineeringCharacterization (materials science)chemistry.chemical_compoundchemistryhyaluronic acid polyaspartamide scaffolds mechanical properties fibroblast attachment.Settore CHIM/09 - Farmaceutico Tecnologico ApplicativoHyaluronic acidPolymer chemistrySelf-healing hydrogelsMaterials ChemistryBiophysics
researchProduct

Characterization of monopolymer blend of virgin and recycled polyamide 6

2002

It is a common industrial practice to blend virgin polymer with the same recycled polymer coming from plastic scraps that, in general, has not undergone relevant degradation. In this work, the characteristics of blends of virgin and recycled polyamide have been considered by changing the amount of recycled polymer and the presence of humidity and a stabilizer. Neither dry nor wet stabilized recycled polyamide samples show significant variations of the molecular weight, but the melt Newtonian viscosity of the blends are slightly different from that predicted by an additive rule, despite the same chemical nature of the two components. This holds true even more for the humid unstabilized sampl…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsHumidityGeneral ChemistryPolymerViscosityCrystallinitySettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiBrittlenesschemistrypolyamide recycling monopolymer blendsPolyamideMaterials ChemistryDegradation (geology)Polymer blendComposite materialPolymer Engineering & Science
researchProduct

Effect of adding new phosphazene compounds to poly(butylene terephthalate)/polyamide blends. II: Effect of different polyamides on the properties of …

2006

Poly(butylene terephthalate) (PBT) and a sample of polyamide have been melt processed in the presence of two new phosphazene compounds, namely 2,2-dichloro-4,4,6,6-bis[spyro(2',2"-dioxy-1',1"-biphenyl)]cyclotriphosphazene (2Cl-CP) and 2,2-bis(2-methoxy-4-methyleneoxy-phenoxy)-4,4,6,6-bis[spyro(2',2"-dioxy-1',1"-biphenyl)]cyclophosphazene (CP-2EPOX). The blends were prepared by using polyamide 6 (PA6) and polyamide 6,6 (PA66) in 25/75 and 75/25 w/w compositions by using a co-rotating twin-screw extruder. The materials have been completely characterized from a mechanical, rheological, and morphological point of view. The results indicate that the additives used cause an increase of the ruptur…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsIzod impact strength testPolymerCompatibilizationPolymer blendCondensed Matter PhysicsCyclophosphazeneReactive compatibilizationchemistry.chemical_compoundSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryPoly(butylene terephthalate)Mechanics of MaterialsPhase (matter)Polymer chemistryPolyamideMaterials ChemistryCopolymerPolyamidePolymer blendPhosphazene
researchProduct

The glass transition behaviour of salted nylon 6

1981

Glass transition measurements of nylon-6/lithium halides mixtures have been carried out in wide range of frequency with the aid of different experimental techniques. The results show an increase of the glass transition temperature when the salt is present and prove the larger effectiveness of lithium chloride with respect of lithium bromide. This effect, in line with the large reduction of the specific volume caused by the salt, is due to the formation of a pseudo-cross-linking between lithium ions and the carbonyl-oxygen groups of the polyamide.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsLithium bromideAnalytical chemistryHalideSalt (chemistry)chemistry.chemical_elementchemistry.chemical_compoundColloid and Surface ChemistryNylon 6chemistryPolyamideMaterials ChemistryLithium chlorideLithiumPhysical and Theoretical ChemistryComposite materialGlass transitionColloid and Polymer Science
researchProduct

Equilibrium swelling and solvation studies on crosslinked polyacrylamides

2004

Polyacrylamide (PA) crosslinked with four different crosslinking agents, triethyleneglycol dimethacrylate (TEGDMA), N,N′-methylene bisacrylamide (NNMBA), hexanediol dimethacrylate (HDDMA) and divinylbenzene (DVB), with mole percents ranging from 5 to 20, was prepared by solution polymerization and subjected to swelling and solvation studies. Solubility parameters and cohesive energy density were determined from swelling studies. Molecular weight between crosslinks for these systems were determined by Flory–Rehner analysis. There is a discontinuous volume change for 10% NNMBA and HDDMA crosslinked PA, 15% TEGDMA crosslinked PA and 10 and 15% DVB crosslinked PA in solvent mixtures of acetic a…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryPolyacrylamideSolvationSolution polymerizationPolymerDivinylbenzenechemistry.chemical_compoundHildebrand solubility parameterchemistrySelf-healing hydrogelsPolymer chemistryMaterials ChemistrymedicineSwellingmedicine.symptomPolymer International
researchProduct

An Improved Rapid Synthesis of Oligo(p -benzamide) Block Copolymers

2008

We describe a new synthesis that allows the preparation of oligo(p-benzamide)s up to the heptamer on solid support without the need of semi-temporary amide N-protective groups. With increase in length, the solubility of oligo(p-benzamide)s reduces dramatically. Even the tetra(p-benzamide) is not soluble in common organic solvents. Therefore, solution syntheses of oligomers beyond the tetramer are not feasible. As will be shown in this paper, solid supported synthesis allows the preparation of even longer oligomers (up to the heptamer) in good yields. The high dilution on the solid support is most likely responsible for their pseudo-solution-like reactivity and the prevention of aggregation.…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistrySupramolecular chemistrySupramolecular polymerschemistry.chemical_compoundchemistryTetramerAmideMaterials ChemistryCopolymerOrganic chemistryReactivity (chemistry)SolubilityBenzamideMacromolecular Rapid Communications
researchProduct

Interpolymer complexes and polymer compatibility.

2012

A reliable method to decide whether two polymers A and B are miscible or incompatible would be very helpful in many ways. In this contribution we demonstrate why traditional procedures cannot work. We propose to use the intrinsic viscosities [η] of the polymer blends instead of the composition dependence of the viscosities as a criterion for polymer miscibility. Two macromolecules A and B are miscible because of sufficiently favorable interactions between the two types of polymer segments. For solutions of these polymers in a joint solvent, this Gibbs energetic preference of dissimilar intersegmental contacts should prevail upon dilution and lead to the formation of interpolymer complexes, …

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsPolymersViscosityIntrinsic viscosityOrganic ChemistryThermodynamicsWaterDextransDimethylformamidePolymerMiscibilityDilutionSolventchemistryPolysaccharidesCompatibility (mechanics)Polymer chemistryMaterials ChemistryPolystyrenesPolyvinylsPolymer blendGlucansMacromoleculeMacromolecular rapid communications
researchProduct

Time-resolved rheology as a tool to monitor the progress of polymer degradation in the melt state - Part I: Thermal and thermo-oxidative degradation …

2015

Abstract Thermal and thermo-oxidative degradation of polyamide 11 (PA11) in the melt state (T = 215 °C) are studied by resorting to time-resolved mechanical spectroscopy. Such an approach allows to elude the changes in the rheological properties occurring while testing, thus enabling the rigorous study of polymer degradation in the melt state. Different concurrent degradation reactions in oxidative (air) and non-oxidative (N2) environment are promptly guessed by studying the time evolutions of rheological functions. In particular, changes in the zero-frequency complex viscosity reflects changes in the average molecular weight, while the appearance of a yield stress in the complex viscosity …

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsRheometryOrganic ChemistrySize-exclusion chromatographyPolymerSECSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiPolymer degradationChemical engineeringRheologychemistryMALDI- TOF-MSPolyamideThermal degradationThermo-oxidative degradationMaterials ChemistryOrganic chemistryDegradation (geology)Molar mass distributionRheologyPolyamide 11
researchProduct

Copolyamides from adipic and truxillic acids: Synthesis and characterization by direct pyrolysis in the mass spectrometer

1977

The synthesis of a series of polyamides and copolyamides containing α-truxillic and adipic units in the chain is reported. The thermal degradation of these polymers was investigated by direct pyrolysis in the ion source of a mass spectrometer. Thermal degradation reactions were followed directly by this method by detecting the thermal- and electron-impact-induced fragments. The results obtained show a good correlation between the intensity of mass peaks characteristic of truxillic and adipic moieties and the composition of the copolyamides, as ascertained by elemental analysis. This is an important result since it shows the potential of the direct pyrolysis method in the analysis of copolym…

chemistry.chemical_classificationMaterials sciencechemistryElemental analysisPolyamideInorganic chemistryCopolymerAnalytical chemistryDegradation (geology)PolymerMass spectrometryPyrolysisIon sourceJournal of Polymer Science: Polymer Chemistry Edition
researchProduct

Conformational properties of N-acetyl-N-methyl-alpha,beta-dehydroalanine N'-methylamide.

2006

The conformational properties of Ac-Delta(Me)Ala-NHMe (N-acetyl-N-methyl-alpha,beta-dehydroalanine N'-methylamide), as the simplest model of N-methyl-alpha,beta-dehydroamino acids, was examined with theoretical methods and in comparison with Ac-DeltaAla-NHMe and Ac-DeltaAla-NMe(2). The N-terminal amide of the Delta(Me)Ala residue easily adopts the configuration cis and the torsion angles phi, psi are highly flexible. The Delta(Me)Ala residue is a conformational flexibilizer as compared to the parent DeltaAla, which is a conformational stiffener. This seems to be the reason why Delta(Me)Ala is found in small natural cyclic peptides, where it ensures the conformational flexibility necessary f…

chemistry.chemical_classificationModels MolecularAlanineMolecular StructureStereochemistryBiophysicsMolecular ConformationHydrogen BondingMethylamideAmidesGeneral Biochemistry Genetics and Molecular BiologyCis trans isomerizationCyclic peptidechemistry.chemical_compoundResidue (chemistry)chemistryModels ChemicalDehydroalanineAmideTheoretical methodsPeptidesActa biochimica Polonica
researchProduct