Search results for "polymers"

showing 10 items of 3567 documents

New biodegradable hydrogels based on a photocrosslinkable modified polyaspartamide: synthesis and characterization

1999

Abstract α,β-Poly( N -2-hydroxyethyl)- dl -aspartamide (PHEA), a synthetic water-soluble biocompatible polymer, was derivatized with glycidyl methacrylate (GMA), in order to introduce in its structure chemical residues having double bonds and ester groups. The obtained copolymer (PHG) contained 29 mol% of GMA residues. PHG aqueous solutions at various concentrations ranging from 30 to 70 mg/ml were exposed to a source of UV rays at λ 254 nm in the presence or in the absence of N , N ′-methylenebisacrylamide (BIS); the formation of compact gel phases was observed beginning from 50 mg/ml. The obtained networks were characterized by FT-IR spectrophotometry and swelling measurements which evide…

Glycidyl methacrylateMagnetic Resonance SpectroscopyDouble bondPolymersUltraviolet RaysBiophysicsBiochemistryEsterasechemistry.chemical_compoundDrug Delivery SystemsEnzymatic hydrolysisSpectrophotometrySpectroscopy Fourier Transform InfraredPolymer chemistrymedicineCopolymerMolecular Biologychemistry.chemical_classificationAcrylamidesAqueous solutionmedicine.diagnostic_testChemistryWaterHydrogelsHydrogen-Ion ConcentrationBiodegradation EnvironmentalSelf-healing hydrogelsEpoxy CompoundsMethacrylatesPeptidesBiochimica et Biophysica Acta (BBA) - General Subjects
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Biodegradable hydrogels obtained by photocrosslinking of dextran and polyaspartamide derivatives

2003

The functionalization of dextran with glycidyl methacrylate (GMA) leads to the formation of a derivative that generates hydrogels for irradiation at 365nm. The effects of various polymer concentrations and irradiation times on the yield and the properties of the obtained hydrogels are reported. The networks have been characterized by FT-IR spectra, dimensional analysis and swelling measurements carried out at different pH values. In vitro studies suggest that all samples undergo a partial chemical hydrolysis, whereas the incubation with dextranases causes a total degradation whose rate depends on the degree of crosslinking. In addition, aqueous solutions of functionalized dextran have been …

Glycidyl methacrylateMaterials scienceMagnetic Resonance SpectroscopyTime FactorsPolymersUltraviolet RaysBiophysicsBiomedical EngineeringBiocompatible MaterialsBioengineeringBiomaterialschemistry.chemical_compoundContraceptive AgentsTheophyllinePolymer chemistrySpectroscopy Fourier Transform InfraredCopolymermedicineBisphenol A-Glycidyl MethacrylateDextranPolyhydroxyethyl MethacrylatePhotocrosslinkingchemistry.chemical_classificationAqueous solutionHydrolysistechnology industry and agricultureTemperatureDextransHydrogelsPolymerDrug releaseHydrogen-Ion Concentrationαβ-Poly(N-2-hydroxyethyl)-DL-aspartamideDextranCross-Linking ReagentschemistryMechanics of MaterialsSelf-healing hydrogelsDrug deliveryCeramics and CompositesSwellingmedicine.symptomPeptidesGlycidyl methacrylateBiotechnology
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New Photosensitive Polymers:  Synthesis and Free Radical Polymerization of Oxypyridinium and Oxyisoquinolinium Functionalized Methacrylate and Styren…

2002

Polymerizable hydroxypyridinium and hydroxyisoquinolinium salts 1a−4a, 2d, and 3d have been prepared from vinylbenzyl chloride or glycidyl methacrylate and 3-hydroxypyridine (2), 4- or 5-hydroxyisoquinoline (1, 3), and 8-hydroxyquinoline (4). Radical homo- and copolymerization with styrene or methyl methacrylate of the salts 1a−3a, 2d, and 3d produced (co)polymers 1e, 2e, 2f, 3f, 1g, 2g, 2h, and 3h. The photosensitive dipolar oxypyridinium or oxyisochinolinium betaine structures were generated in solutions with triethylamine from the low molecular weight and polymeric salt precursors. For the model compounds 1b−4b and (co)polymers 1e, 2e, 2f, 3f, 1g, 2g, 2h, and 3h, the degradation of the l…

Glycidyl methacrylatePolymers and PlasticsOrganic ChemistryRadical polymerizationPhotochemistryMethacrylatePolyelectrolyteStyreneInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCopolymerMethyl methacrylateTriethylamineMacromolecules
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Extraction of β-blockers from urine with a polymeric monolith modified with 1-allyl-3-methylimidazolium chloride in spin column format

2020

Abstract A glycidyl methacrylate-based monolith was modified with imidazolium-based ionic liquid (IL) to be used as stationary phase for solid-phase extraction (SPE). The host monolithic support was prepared by in-situ UV polymerization in spin column format. Two approaches were developed to incorporate the IL into the polymeric monolithic matrix: generation of IL onto the surface monolith, and copolymerization by addition of the IL to the polymerization mixture, which gave the best results. The resulting sorbent materials were morphologically characterized and used for the isolation of five β-blockers from human urine samples. All SPE steps were accomplished by centrifugation, which reduce…

Glycidyl methacrylatePolymersSurface PropertiesAdrenergic beta-Antagonists02 engineering and technology01 natural sciencesHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundSpin column-based nucleic acid purificationHumansSolid phase extractionParticle SizeMonolithDetection limitgeographygeography.geographical_feature_categoryChromatographyChemistrySolid Phase Extraction010401 analytical chemistryExtraction (chemistry)Imidazoles021001 nanoscience & nanotechnology0104 chemical sciencesAllyl CompoundsEpoxy CompoundsMethacrylates0210 nano-technologyTalanta
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Green Design of Novel Starch-Based Packaging Materials Sustaining Human and Environmental Health

2021

A critical overview of current approaches to the development of starch-containing packaging, integrating the principles of green chemistry (GC), green technology (GT) and green nanotechnology (GN) with those of green packaging (GP) to produce materials important for both us and the planet is given. First, as a relationship between GP and GC, the benefits of natural bioactive compounds are analyzed and the state-of-the-art is updated in terms of the starch packaging incorporating green chemicals that normally help us to maintain health, are environmentally friendly and are obtained via GC. Newer approaches are identified, such as the incorporation of vitamins or minerals into films and coati…

Green chemistryMaterials sciencePolymers and PlasticsGreen nanotechnologyStarchResearch areasnanopackagingNanotechnologyReview02 engineering and technologycold plasmalcsh:QD241-441chemistry.chemical_compound0404 agricultural biotechnologygreen technologylcsh:Organic chemistrySustainable designMetal nanoparticlesbioactivegreen packaginggreen chemistrystarchhealth04 agricultural and veterinary sciencesGeneral Chemistry021001 nanoscience & nanotechnology040401 food scienceEnvironmentally friendlyUVchemistrybioinspirationBioinspiration0210 nano-technologyPolymers
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New approach for synthesis of poly(ethylglyoxylate) using Maghnite-H + , an Algerian proton exchanged montmorillonite clay, as an eco-catalyst

2017

International audience; In this works, we have explored a new method for a green synthesis of poly(ethylglyoxylate) (PEtG). This method consists on using a montmorillonite clay called Maghnite-H+ as an eco-catalyst to replace triethylamine which is toxic. Cationic polymerization experiments are performed in bulk conditions at three temperatures (-40 degrees C, 25 degrees C, 80 degrees C) and in THF solutions at room temperature (25 degrees C). At 25 degrees C, an optimum ratio of 5 wt% of catalyst leads to molar masses up to 22000 g/mol in THF solutions. Polymerizations in bulk conditions lead to slightly lower masses than experiments conducted in THF solutions. However, bulk polymerization…

Green chemistryThermogravimetric analysisMaterials scienceepsilon-caprolactonePolymers and PlasticsBulk polymerizationMaghnite-H+ring-opening polymerization02 engineering and technologyEthylglyoxylate010402 general chemistry7. Clean energy01 natural sciencesalcoholschemistry.chemical_compoundbiodegradable plasticsMaterials Chemistrycationic polymerizationionic polymerizationsThermal stabilityComposite materialsheet silicatespoly(methyl glyoxylate)degradationchemistry.chemical_classificationMolar masscopolymergreen chemistrybis-macromonomersCationic polymerizationbiodegradable polymerGeneral ChemistryPolymer021001 nanoscience & nanotechnology0104 chemical sciences[ CHIM.POLY ] Chemical Sciences/PolymersMontmorillonite[CHIM.POLY]Chemical Sciences/PolymersChemical engineeringchemistryCeramics and Compositeseco-catalyst0210 nano-technology
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Undecylenic acid: A tunable bio-based synthon for materials applications

2016

International audience; An undecylenic acid-based monoglyceride prepared from glycidol and undecylenic acid is used as suitable and tunable synthon for polymerization applications. Epoxidation and acrylation reactions lead to photopolymerizable monomers while transesterification with dimethyl carbonate, metathesis and aminolysis reactions provide access to polyhydroxyurethane-based materials. The successive intermediates were synthesized according to a green chemistry approach implicating solvent-less and catalyzed reactions, and were at each step fully characterized by infrared, 1H and 13C{1H} NMR spectroscopy, elemental analysis and mass spectrometry. Analyses of the resulting polymer mat…

Green chemistryThermogravimetric analysisRenewable resourcesMaterials sciencePolymers and PlasticsOrganic carbonatepolyhydroxyurethanespolyurethanesGeneral Physics and Astronomy02 engineering and technologycyclic carbonates010402 general chemistry01 natural sciences[ CHIM ] Chemical Scienceschemistry.chemical_compoundPolyhydroxyurethanes (PHUs)Aminolysisrenewable building-blockPolymer chemistryMaterials ChemistrymedicineOrganic chemistry[CHIM]Chemical Sciencessolvent-free conditionscastor-oilglycerol carbonatePhotopolymerizationOrganic ChemistrySynthonGlycidolTransesterification021001 nanoscience & nanotechnologyFatty acid0104 chemical scienceschemistryPolymerizationGlycidolpolycarbonatespolymerizationUndecylenic acidderivatives0210 nano-technologymedicine.drug
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Der Einfluß des Raumbedarfs der Kristallite auf die Entropie teilkristalliner Hochpolymerer

1966

Es werden Gleichungen fur die Konformationsentropie der Kettenteile in den nichtkristallinen Bereichen abgeleitet, wobei auch die Volumenbegrenzung dieser Bereiche durch die Kristallite berucksichtigt wird. Hierzu mus ein dreidimensionales Irrflugproblem bei Anwesenheit von absorbierenden Wanden gelost werden. Es zeigt sich, das die Volumenbegrenzung die Entropie der Kettenteile in den nichtkristallinen Bereichen wesentlich vermindert. Im Anschlus an diese Berechnungen werden die Auswirkungen der untersuchten Entropieeffekte auf die Kristallkeimbildung und das Schmelzen diskutiert. Bei der Kristallkeimbildung haben die Entropieeffekte zur Folge, das ein Buschelkeim eine bedeutend grosere Ke…

GynecologyPhysicsmedicine.medical_specialtyColloid and Surface ChemistryPolymers and PlasticsMaterials ChemistrymedicinePhysical and Theoretical ChemistryKolloid-Zeitschrift & Zeitschrift für Polymere
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Über Zusammenhänge zwischen der Röntgenkleinwinkelstreuung und der morphologischen Struktur verstreckter Hochpolymerer

1968

In der vorliegenden Arbeit wird uber Versuche berichtet, die Ergebnisse der Rontgenkleinwinkelstreuung an verstreckten Hochpolymeren mit Hilfe von elektronenmikroskopisch beobachtbaren Strukturen zu deuten. Geeignet behandelte elektronenmikroskopische Aufnahmen lassen sich als optische Gitter fur Lichtbeugungsversuche verwenden. Die daran erhaltenen Lichtbeugungsdiagramme zeigen eine Intensitatsverteilung, die mit der rontgenographisch gemessenen gut ubereinstimmt. Es lies sich zeigen, das die elektronenmikroskopisch an verschiedenen verstreckten Hochpolymeren (Polyathylen, Polyoxymethylen und Polyathylenterephthalat) gefundenen periodischen Querstrukturen nicht nur ihrem mittleren Abstand …

GynecologyPhysicsmedicine.medical_specialtyColloid and Surface ChemistryPolymers and PlasticsMaterials ChemistrymedicinePhysical and Theoretical ChemistryKolloid-Zeitschrift & Zeitschrift für Polymere
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Umwandlungserscheinungen in amorphen Hochpolymeren beim tempern unterhalb der Glastemperatur

1968

Es wird die zeitliche Anderung der mechanischen Eigenschaften von amorphem PC, PET und PMMA beim isothermen Tempern unterhalb der Glastemperatur untersucht. Dabei ergab sich, das von der Glastemperatur abgeschrecktes Material beim Tempern ein stufenweises Ansteigen des Schubmoduls zeigt, das von einer Abnahme der Dampfung begleitet ist. Kurzzeitiges Uberschreiten der Glastemperatur mit nachfolgendem Abschrecken macht die durch das Tempern bewirkten Anderungen ruckgangig. Die Beobachtungen werden als Platzwechsel von Kettensegmenten im Sinne einer Ausbildung von lokal begrenzten Bereichen hoherer Dichte gedeutet, die sich beim Uberschreiten der Glastemperatur wieder auflosen.

GynecologyPhysicsmedicine.medical_specialtyColloid and Surface ChemistryPolymers and PlasticsMaterials ChemistrymedicinePhysical and Theoretical ChemistryKolloid-Zeitschrift & Zeitschrift für Polymere
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