Search results for "methacrylic acid"

showing 10 items of 71 documents

Radiation grafting functionalization of poly (vinylidene fluoride) to compatibilize its blends with polyolefin ionomers

1998

Blends of a crystalline vinylidene fluoride copolymer (PVDF) and a polyolefin ionomer were produced by melt mixing and characterized by a variety of techniques to examine the effect of increasing the level of salt formation on morphology. The PVDF component was also grafted with methacrylic acid by irradiating the polymer powder and subsequently treating it with an aqueous monomer solution. The effect of neutralizing the acid in both polymer components to produce the corresponding zinc salt was also investigated. Compatibilization was accomplished by the addition of zinc acetyl acetonate (ZnAcAc) to the mixture. This increased the viscosity of the polyolefin ionomer phase, comparable to tha…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsGeneral ChemistryPolymerCompatibilizationPolyolefinchemistry.chemical_compoundMonomerchemistryMethacrylic acidPolymer chemistryMaterials ChemistryCopolymerPolymer blendIonomerPolymer Engineering & Science
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Oligo(glycerol) Methacrylate Macromonomers

2011

Linear, protected ω-methoxy oligo(glycerol) methacrylate (OGly(P)MA) macromonomers are synthesized via anionic ring-opening polymerization of ethoxyethyl glycidyl ether (EEGE) followed by termination with methacrylic acid anhydride (DP(n) = 3-11, PDI < 1.30). The covalently bound methacrylate moiety allows the homopolymerization of OGly(P)MA as well as copolymerization with low molecular weight comonomers. In homopolymerizations, macromonomers are polymerized by atom transfer radical polymerization (ATRP) yielding well-defined graft polymers (M(n) = 20,000-30,000 g mol(-1)). Acidic hydrolysis of the protecting groups releases water-soluble polyhydroxy-functional structures. First results on…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsPolymersAtom-transfer radical-polymerizationHydrolysisOrganic ChemistryPolymerMethacrylateHydrolysischemistry.chemical_compoundchemistryPolymerizationMethacrylic acidPolymer chemistryMaterials ChemistryCopolymerMethacrylatesMoietyEthersMacromolecular Rapid Communications
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Characterization of Micelles of Polyisobutylene-block-poly(methacrylic acid) in Aqueous Medium

2000

Four amphiphilic block copolymers polyisobutylene-block-poly(methacrylic acid) (IBm-MAAn; m = 70−134, n = 52−228) were synthesized and transferred into aqueous medium at pH 10−12. Their structure in solution was characterized by fluorescence correlation spectroscopy (FCS), static and dynamic light scattering (SLS, DLS), analytical ultracentrifuge (AUC), and by transmission electron microscopy (TEM) with freeze-fracturing and staining techniques. DLS data, AUC sedimentation traces, and TEM images indicate at least two different kinds of particles. TEM shows spherical micelles; however, especially for polymers with larger hydrophobic blocks, additional particles are observed. FCS shows extrem…

chemistry.chemical_classificationPoly(methacrylic acid)Aqueous solutionPolymers and PlasticsOrganic ChemistryAnalytical chemistryFluorescence correlation spectroscopyPolymerMicelleInorganic Chemistrychemistry.chemical_compoundchemistryMethacrylic acidDynamic light scatteringPolymer chemistryMaterials ChemistryCopolymerMacromolecules
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1992

chemistry.chemical_classificationPoly(methacrylic acid)Aqueous solutionSalt (chemistry)Block (periodic table)Chloridechemistry.chemical_compoundchemistryPhase (matter)Polymer chemistryCopolymermedicine1-methyl-4-vinylpyridiniummedicine.drugDie Makromolekulare Chemie, Rapid Communications
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Concentration-dependent switch between chain association and dissociation of oppositely charged weak polyelectrolytes in solution

2019

Abstract Joint solutions of oppositely charged weak polyelectrolytes are considerably less studied than their strong counterparts; as a result, their thermodynamic understanding is still unsatisfactory. This shortcoming hampers the development of a general picture about the physical properties of these mixtures, which further hampers their use to design new materials. To close this gap, we investigate the ternary system ethanol/polyacid/polybase (polyacid: methacrylic acid containing copolymer; polybase: N,N-dimethylaminoethyl methacrylate containing terpolymer) with respect to its demixing and viscometric behavior. Complete homogeneity can only be reached if the total polymer concentration…

chemistry.chemical_classificationTernary numeral systemPolymers and PlasticsOrganic Chemistry02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnologyMethacrylate01 natural sciencesDissociation (chemistry)Polyelectrolyte0104 chemical sciencesDegree of ionizationchemistry.chemical_compoundMethacrylic acidchemistryChemical physicsMaterials ChemistryCopolymer0210 nano-technologyPolymer
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pH-sensitive hydrogel based on a polyaspartamide derivative

2006

A pH-sensitive hydrogel was prepared by UV irradiation technique. Starting polymer was obtained from alpha,beta-poly (N-2-hydroxyethyl)-DL-aspartamide (PHEA) partially derivatized with glycidyl methacrylate (PHG). The PHG copolymer was cross-linked by UV irradiation in the presence of methacrylic acid (MA) to form a pH sensitive hydrogel. The cross-linked matrix shaped as microparticles was characterized by FT-IR spectrophotometry, XPS, X-ray diffraction, SEM and particle size distribution analyses. Moreover, to have information about water affinity of the prepared sample, swelling measurements were carried out in aqueous media mimicking some biological fluids. In order to employ the prepar…

chemistry.chemical_classificationalphabeta-poly (N-2-hydroxyethyl)-DL-aspartamideGlycidyl methacrylateMaterials sciencemethacrylic acidPharmaceutical SciencePolymerDosage formpH-sensitive hydrogelchemistry.chemical_compoundPhotopolymerchemistryMethacrylic acidDrug deliveryPolymer chemistryphotopolymerizationdrug deliverymedicineCopolymerSwellingmedicine.symptomdrug deliveryalphabeta-poly (N-2-hydroxyethyl)-DL-aspartamideNuclear chemistry
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Target Analogue Imprinted Polymers with Affinity for Folic Acid and Related Compounds

2001

Two approaches to synthesize molecularly imprinted polymers with affinity for folic acid and other substituted pteridines have been compared. In the first approach, the folic acid analogue methotrexate was used as template and functional monomers capable of generating selective binding sites were searched in a miniaturized screening system based on binding assessment in the batch mode. Highest selectivity was seen using 2-vinylpyridine as functional monomer, which was confirmed in the chromatographic mode for a batch synthesized on a gram scale. However, the retentivity and selectivity of this phase were insufficient for anticipated applications. In a second approach, using methacrylic acid…

chemistry.chemical_classificationbiologyPolymersPteridinesMolecularly imprinted polymerGeneral ChemistryPolymerBiochemistryCatalysischemistry.chemical_compoundFolic AcidMethotrexateColloid and Surface ChemistryEnzymeMethacrylic acidchemistryDihydrofolate reductasemedicinebiology.proteinOrganic chemistryBinding siteSelectivityPteridinemedicine.drugJournal of the American Chemical Society
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Die zweifache unterdrückung der polymerisation einiger bis(methacrylsäureester) mittels radikalischer additionsreaktionen

1973

Aus Hydrochinon, Resorcin, Dihydroxydiphenylen und Dihydroxynaphthalinen wurden mit Methacrylsaurechlorid Bis(methacrylsaureester) hergestellt. Setzte man diese in siedendem Benzol mit groser Verdunnung gelosten Ester dem Angriff von Radikalen aus α.α′-Azoisobuttersauredinitril (Primarradikale) aus, dessen Uberschus in Beziehung zum Ester mindestens zwanzigfach molar war, so erhielt man mittels saulenchromatographischer Trennung Verbindungen, bei denen je olefinische Doppelbindung zwei Primarradikale addiert waren (unterdruckte Polymerisation). Die Struktur dieser Produkte wurde mittels Elementaranalyse, Molekulargewichtsbestimmung, IR- und 1H-NMR-Spektren bewiesen. Demnach kann die Polymer…

chemistry.chemical_classificationchemistry.chemical_compoundMolar concentrationColumn chromatographychemistryHydroquinoneMethacrylic acidDouble bondPolymerizationRadicalPolymer chemistryResorcinolDie Makromolekulare Chemie
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Studies on the Process of Formation, Nature and Stability of Binding Sites in Molecularly Imprinted Polymers

2002

AbstractIn Molecular Imprinting the nature of the templated binding sites and the mechanism of their formation are still poorly understood. For this reason our groups are carrying out fundamental studies concerning known imprinting protocols, with the primary aim of shedding light on the role of the template in the different steps of the polymerisation, from the formation of primary chains to the build-up of the porous structure. In this paper we report our initial results concerning copolymers of methacrylic acid (MAA) and ethyleneglycol dimethacrylate (EDMA) and their formation in presence or absence of the templates 9-ethyladenine, ametryn or terbutylazine. Monitoring the monomer disappe…

chemistry.chemical_classificationchemistry.chemical_compoundMonomerMaterials scienceMethacrylic acidchemistryPolymerizationPolymer chemistrySize-exclusion chromatographyMolecularly imprinted polymerPolymerMethacrylateMolecular imprintingMRS Proceedings
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Enantioselective Ester Hydrolysis Catalyzed by Imprinted Polymers. 2,

2000

Highly cross-linked network polymers prepared by molecular imprinting catalyzed enantioselectively the hydrolysis of N-tert-butoxycarbonyl phenylalanine-p-nitrophenyl ester (BOCPheONP). The templates were designed to allow incorporation of the key catalytic elements, found in the proteolytic enzyme chymotrypsin, into the polymer active sites. Three model systems were evaluated. These were constructed from a chiral phosphonate analogue of phenylalanine (series A, C) or L-phenylalanine (series B) attached by a labile ester linkage to an imidazole-containing vinyl monomer. Free radical copolymerization of the template with methacrylic acid (MAA) and ethylene glycol dimethacrylate (EDMA) gave a…

chemistry.chemical_classificationchemistry.chemical_compoundMonomerchemistryMethacrylic acidHydrogen bondEthylene glycol dimethacrylateOrganic ChemistryPolymer chemistryProteolytic enzymesCarboxylatePolymerMolecular imprintingThe Journal of Organic Chemistry
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