Search results for "Glycidyl ether"

showing 10 items of 22 documents

Analytical strategies for organic food packaging contaminants

2016

In this review, we present current approaches in the analysis of food-packaging contaminants. Gas and liquid chromatography coupled to mass spectrometry detection have been widely used in the analysis of some relevant families of these compounds such as primary aromatic amines, bisphenol A, bisphenol A diglycidyl ether and related compounds, UV-ink photoinitiators, perfluorinated compounds, phthalates and non-intentionally added substances. Main applications for sample treatment and different types of food-contact material migration studies have been also discussed. Pressurized Liquid Extraction, Solid-Phase Microextraction, Focused Ultrasound Solid-Liquid Extraction and Quechers have been …

Bisphenol AChromatography GasPhthalic AcidsFood ContaminationChemical Fractionation010501 environmental sciencesQuechersMass spectrometry01 natural sciencesBiochemistryMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundPhenolsSample preparationBenzhydryl CompoundsBisphenol A diglycidyl ether0105 earth and related environmental sciencesPrimary (chemistry)ChromatographyChemistry010401 analytical chemistryOrganic ChemistryExtraction (chemistry)Food PackagingGeneral Medicine0104 chemical sciencesFood packagingEnvironmental chemistryEpoxy CompoundsChromatography LiquidJournal of Chromatography A
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Study of the Curing Process of DGEBA Epoxy Resin Through Structural Investigation

2015

In this work, a multi-scale approach with different analytical methods is applied to study the curing process and the structural properties of a diglycidyl ether of bisphenol A (DGEBA) epoxy resin. This monomer, thermally cured using 4,4′-diaminodiphenilsulfone (DDS) as hardener, is analyzed after 10, 45, 90, and 120 min of reaction time at 180 °C to obtain information on samples with different cross-linking densities. Samples are also characterized after extraction in acetone in order to obtain structural information on the insoluble parts. For this purpose, differential scanning calorimetry (DSC), dynamic mechanical thermal analysis (DMTA), solid-state nuclear magnetic resonance (ss-NMR),…

Bisphenol AMaterials scienceDiglycidyl etherEpoxy resins solid-state nuclear magnetic resonance (ss-NMR) positron annihilation lifetime spectroscopy (PALS)Polymers and PlasticsOrganic ChemistryEpoxyDynamic mechanical analysisCondensed Matter Physicschemistry.chemical_compoundMonomerDifferential scanning calorimetrychemistrySolid-state nuclear magnetic resonancevisual_artPolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysical and Theoretical ChemistryThermal analysis
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Design and synthesis of biobased epoxy thermosets from biorenewable resources

2017

International audience; Biobased diepoxy synthons derived from isoeugenol, eugenol or resorcinol (DGE-isoEu, DGE-Eu and DGER, respectively) have been used as epoxy monomers in replacement of the diglycidyl ether of bisphenol A (DGEBA). Their curing with six different biobased anhydride hardeners leads to fully biobased epoxy thermosets. These materials exhibit interesting thermal and mechanical properties comparable to those obtained with conventional petrosourced DGEBA-based epoxy resins cured in similar conditions. In particular, a high Tg in the range of 90–130 °C and instantaneous moduli higher than 4.3 GPa have been recorded. These good performances are very encouraging, making these n…

Bisphenol AMaterials scienceDiglycidyl etherGeneral Chemical EngineeringThermosetting polymer02 engineering and technologyResorcinol010402 general chemistry01 natural sciences[ CHIM ] Chemical SciencesNanoindentationchemistry.chemical_compound[CHIM] Chemical SciencesPolymer chemistry[CHIM]Chemical SciencesComputingMilieux_MISCELLANEOUSCuring (chemistry)Biobased resinsPolymer scienceCuring process[CHIM.MATE]Chemical Sciences/Material chemistryGeneral ChemistryEpoxy021001 nanoscience & nanotechnology0104 chemical sciencesDEGBA alternativeIsoeugenolMonomerchemistryvisual_artvisual_art.visual_art_medium0210 nano-technologyEpoxy-anhydride thermosets
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Preferential solvation of poly(methyl methacrylate) and a bisphenol A diglycidyl ether by size-exclusion chromatography

2004

The preferential adsorption coefficient, lambda, of poly(methyl methacrylate), PMMA, in solutions formed by an epoxy resin in tetrahydrofuran (THF), was studied by size-exclusion chromatography (SEC). Only PMMA of lowest molar mass was preferentially solvated by epoxy but at low concentrations of epoxy in the mixture. At higher epoxy content PMMA was preferentially solvated by THF. A simultaneous and competitive solvation between the specific interactions PMMA-epoxy and the self association of epoxy at high concentrations would be the responsible of this inversion point. The more compacted coil of PMMA of higher molecular weights in solution could explain the lack of interaction of these po…

Chemical PhenomenaSize-exclusion chromatographymacromolecular substancesBiochemistryAnalytical ChemistryGel permeation chromatographychemistry.chemical_compoundPolymer chemistryPolymethyl MethacrylateBenzhydryl CompoundsMethyl methacrylateFuransBisphenol A diglycidyl etherTetrahydrofuranChromatographyMolar massChemistry PhysicalOrganic Chemistrytechnology industry and agricultureGeneral MedicineEpoxyequipment and suppliesPoly(methyl methacrylate)Molecular Weightbody regionsSolubilitychemistryvisual_artCalibrationChromatography Gelvisual_art.visual_art_mediumEpoxy CompoundsAlgorithmsJournal of Chromatography
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Determination of bisphenol diglycidyl ether residues in canned foods by pressurized liquid extraction and liquid chromatography–tandem mass spectrome…

2005

Abstract A new confirmatory method for simultaneous determination of bisphenol diglycidyl ether residues (BADGE, BADGE·H2O, BADGE·2H2O, BADGE·H2O·HCl, BADGE·HCl, BADGE·2HCl, BFDGE and BFDGE·2HCl) from canned food has been developed. The proposed method includes extraction by pressurized liquid extraction (PLE) followed by liquid–liquid partition and purification by solid phase extraction (SPE). Several solvent systems and different operating conditions (time, temperature) have been investigated for PLE optimization. A reversed-phase high-performance liquid chromatography (RP-HPLC) coupled to atmospheric pressure chemical ionisation tandem mass spectrometry (APCI-MS–MS) method was developed …

Chemical ionizationDiglycidyl etherChromatographyBisphenolOrganic ChemistryTemperatureAtmospheric-pressure chemical ionizationGeneral MedicineBiochemistryHigh-performance liquid chromatographyMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundAtmospheric PressurechemistryLiquid chromatography–mass spectrometrySolventsEpoxy CompoundsSolid phase extractionBenzhydryl CompoundsBisphenol A diglycidyl etherChromatography High Pressure LiquidFood AnalysisJournal of Chromatography A
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Aqueous Processed Biopolymer Interfaces for Single-Cell Microarrays

2020

Single-cell microarrays are emerging tools to unravel intrinsic diversity within complex cell populations, opening up new approaches for the in-depth understanding of highly relevant diseases. However, most of the current methods for their fabrication are based on cumbersome patterning approaches, employing organic solvents and/or expensive materials. Here, we demonstrate an unprecedented green-chemistry strategy to produce single-cell capture biochips onto glass surfaces by all-aqueous inkjet printing. At first, a chitosan film is easily inkjet printed and immobilized onto hydroxyl-rich glass surfaces by electrostatic immobilization. In turn, poly(ethylene glycol) diglycidyl ether is graft…

Diglycidyl etherMaterials scienceFabrication0206 medical engineeringBiomedical EngineeringBiointerfaceNanotechnology02 engineering and technologyengineering.materialArticleBiomaterialsChitosanchemistry.chemical_compoundBiopolymersbiopolymerbiointerfaceHumansBiochipMicroscale chemistrySettore CHIM/02 - Chimica Fisicainkjet printingsingle-cellMicroarray Analysis021001 nanoscience & nanotechnology020601 biomedical engineeringSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Inkjet printing biopolymer single-cell microarray biointerfacechemistryengineeringGlassBiopolymer0210 nano-technologymicroarrayEthylene glycol
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2020

Epoxy resin plays a key role in composite matrices and DGEBA is the major precursor used. With the aim of favouring the use of bio resources, epoxy resins can be prepared from lignin. In particular, diglycidyl ether of isoeugenol derivatives are good candidates for the replacement of DGEBA. This article presents an effective and eco-friendly way to prepare epoxy resin derived from isoeugenol (BioIgenox), making its upscale possible. BioIgenox has been totally characterized by NMR, FTIR, MS and elemental analyses. Curing of BioIgenox and camphoric anhydride with varying epoxide function/anhydride molar ratios has allowed determining an optimum ratio near 1/0.9 based on DMA and DSC analyses a…

Diglycidyl etherMaterials sciencePolymers and PlasticsComposite numberThermosetting polymer02 engineering and technologyGeneral ChemistryEpoxyDynamic mechanical analysis010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistry.chemical_compoundIsoeugenolChemical engineeringchemistryvisual_artUltimate tensile strengthvisual_art.visual_art_medium0210 nano-technologyCuring (chemistry)Polymers
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From an epoxide monomer toolkit to functional PEG copolymers with adjustable LCST behavior.

2011

The lower critical solution temperature (LCST) behavior of novel poly(ethylene glycol) (PEG)-based copolymers bearing multiple functional groups, obtained by anionic ring-opening (co)polymerization (AROP), has been investigated. Variable comonomer ratios of ethylene oxide (EO) and the corresponding oxiranes isopropylidene glyceryl glycidyl ether (IGG), ethoxyl vinyl glycidyl ether (EVGE), allyl glycidyl ether (AGE), or N,N-dibenzyl amino glycidyl (DBAG), particularly designed to implement functional groups at the PEG backbone, were found to influence the LCST behavior. Sharp transitions from translucent to opaque solutions, comparable to other well-established stimuli-responsive polymers, w…

Ethylene OxideMaterials scienceHot TemperaturePolymers and PlasticsPolymersAllyl glycidyl etherpolyethersEpoxideLower critical solution temperaturePolymerizationPolyethylene Glycolschemistry.chemical_compoundPolymer chemistrycopolymersMaterials ChemistryCopolymerPoly(Ethylene Glycol) CopolymersSide-ChainsAqueous-SolutionEthylene oxideComonomerstimuli-sensitiveOrganic ChemistryPegchemistryPolymerizationGlycidolLcstEthylene glycolHydrophobic and Hydrophilic InteractionsMacromolecular rapid communications
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Poly(ethylene glycol-co-allyl glycidyl ether)s: a PEG-based modular synthetic platform for multiple bioconjugation.

2011

A series of random copolymers comprising ethylene oxide (EO) and 0-100% allyl glycidyl ether (AGE) has been prepared by anionic ring-opening polymerization with molecular weights between 5000 and 13,600 g/mol and polydispersity indices in the range of 1.04-1.19. As key for the homogeneity of the PEG conjugates, real-time ¹H NMR polymerization kinetics, ¹³C NMR analysis of triad sequence distribution, and analysis of the thermal behavior by differential scanning calorimetry (DSC) revealed a distinctive random copolymer structure. Via thiol-ene coupling (TEC), showing mainly "click" characteristics and nearly quantitative yields, PEG derivatives with multiple amino, carboxy, or hydroxy functi…

Magnetic Resonance SpectroscopyAllyl glycidyl etherDispersityBiomedical EngineeringPharmaceutical ScienceBioengineeringTripeptideCatalysisPolyethylene GlycolsPolymerizationchemistry.chemical_compoundPolymer chemistryPEG ratioCopolymerSulfhydryl CompoundsPharmacologyEthylene oxideChemistryOrganic ChemistryTemperatureNuclear magnetic resonance spectroscopyKineticsPolymerizationEpoxy CompoundsPeptidesBiotechnologyBioconjugate chemistry
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Curing of an epoxy resin modified with nanoclay monitored by dielectric spectroscopy and rheological measurements

2006

Dielectric and rheological measurements have been performed in “real-time” to follow curing reaction on blends of a diglycidyl ether of bisphenol-A epoxy resin with 4,4-methylene bis(2,6-diethylaniline) hardener and different amounts of organically modified nanoclay (Nanofil 919) as modifier. The effect of the modifier and its amount on the curing reaction, as well as that of the curing temperature has been studied. Changes in molecular mobility in the reaction mixture have been investigated by dielectric relaxation spectroscopy. Evolutions of ionic conductivity and main relaxation have been analyzed and vitrification times have been obtained and compared with those obtained by rheological …

Materials scienceDiglycidyl etherNanocompositePolymers and PlasticsThermosetting polymerGeneral ChemistryEpoxyDielectricSurfaces Coatings and FilmsDielectric spectroscopychemistry.chemical_compoundchemistryvisual_artMaterials Chemistryvisual_art.visual_art_mediumOrganoclayComposite materialCuring (chemistry)Journal of Applied Polymer Science
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