Search results for "PLASTICS"

showing 10 items of 2724 documents

Enzymatically catalyzed synthesis of photocrosslinkable oligophenols

2000

The HRP-catalyzed oligomerization of cinnamoyl-hydroquinone-ester and cinnamoyl-4-hydroxyanilide led to the formation of soluble polyphenols. The oligomers were synthexized in water/1,4-dioxane and in water/acetone mixtures and characterized by NMR, FTIR and SEC. Upon UV treatment of the homogenoes films the polyphenols were crosslinked due to [2+2]-cycloadditions of the cinnamoyl functions.

Polymers and PlasticsbiologyOrganic ChemistryCondensed Matter PhysicsOligomerCatalysisEnzyme catalysischemistry.chemical_compoundchemistryPhotosensitivityPolyphenolPolymer chemistryMaterials ChemistryAcetonebiology.proteinOrganic chemistryPhenolsPhysical and Theoretical ChemistryPeroxidaseMacromolecular Chemistry and Physics
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Influence of interactions on water and aroma permeabilities of ι-carrageenan–oleic acid–beeswax films used for flavour encapsulation

2009

The objective of this work is to investigate the water and aroma barrier properties of films obtained from ι-carrageenan containing glycerol and lipids mixtures of oleic acid (OA) and beeswax (BW) used for encapsulation of active compounds. Water vapor permeability (WVP) is greatly influenced by lipid composition, encapsulated aroma compound and also relative humidity. WVP decreases when films contain encapsulated aroma compound but increases when the moisture content in the films increases. When oleic acid was the main compound of lipid phase, the plasticizing effect of water revealed through water permeability is less marked. The results of ethyl acetate, ethyl butyrate, ethyl hexanoate, …

Polymers and PlasticsbiologyOrganic ChemistryEthyl acetatefood and beveragesEthyl hexanoatePermeationbiology.organism_classificationchemistry.chemical_compoundOleic acidchemistryEthyl butyrateMaterials ChemistryGlycerolAroma compoundOrganic chemistryAromaCarbohydrate Polymers
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Polyphosphate: A Morphogenetically Active Implant Material Serving as Metabolic Fuel for Bone Regeneration

2015

The initial mineralization centers during human bone formation onto osteoblasts are composed of CaCO3 . Those bioseeds are enzymatically formed via carbonic anhydrase(s) in close association with the cell surface of the osteoblasts. Subsequently, the bicarbonate/carbonate anions are exchanged non-enzymatically by inorganic phosphate [Pi ]. One source for the supply of Pi is polyphosphate [polyP] which is a physiological polymer, formed in the osteoblasts as well as in the platelets. The energy-rich acid anhydride bonds within the polyP chain are cleaved by phosphatase(s); during this reaction free-energy might be released that could be re-used, as metabolic fuel, for the maintenance of the …

Polymers and PlasticsbiologyPolyphosphateBicarbonatePhosphataseBioengineeringMineralization (biology)Acid anhydrideBiomaterialschemistry.chemical_compoundchemistryBiochemistryTissue engineeringCarbonic anhydraseMaterials Chemistrybiology.proteinBone regenerationBiotechnologyMacromolecular Bioscience
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Correlation of the Extent of Fjord-Region Oxidation with DNA Binding and Mutagenicity of the Enantiomeric 11,12-Dihydrodiols of Dibenzo[a,l]pyrene

1996

Abstract In vitro studies on the hepatic biotransformation of the enantiomeric trans-11,12-dihydrodiols of dibenzo[a,l]pyrene (DB[a,l]P) using microsomal fractions of animals pretreated with Aroclor 1254 revealed that the formation of fjord-region dihydrodiol epoxides strongly depends on the absolute configuration of the substrate. Both the (-)-11R,12R- and the (+)-11S,12S-enantiomer are converted diastereoselectively to the (-)- and (+)-anti-dihydrodiol epoxide, respectively, by either rat or mouse liver microsomes. Fjord-region oxidation occurs to greatest extent on incubation of the (-)-11R,12R-dihydrodiol with preparations from rats. This finding is in line with the differences seen for…

Polymers and PlasticsbiologyStereochemistryOrganic ChemistryAbsolute configurationSubstrate (chemistry)Epoxidebiology.organism_classificationChinese hamsterchemistry.chemical_compoundchemistrypolycyclic compoundsMaterials ChemistryMicrosomePyreneEnantiomerDNAPolycyclic Aromatic Compounds
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Diffusion in concentrated colloidal suspensions and glasses

1998

The well established analogy between colloidal suspensions and atomic fluids has been extended to the glass transition problem in the past few years. Colloids have become the ideal test case for checking glass transition theories; this was due to the possibility of modeling hard spheres with colloidal dispersions. Significant progress has also been made in instrumentation, especially in the development of light-scattering techniques allowing moderately turbid and nonergodic samples to be analyzed. Mode coupling theory has become a paradigm not only for the glass transition, but also for the understanding of dynamics in highly concentrated colloidal dispersions where crystallization is suppr…

Polymers and Plasticsbusiness.industryChemistryDiffusiondigestive oral and skin physiologySurfaces and InterfacesHard spheresLight scatteringlaw.inventionCondensed Matter::Soft Condensed MatterColloidColloid and Surface ChemistryOpticsOptical microscopelawChemical physicsMode couplingPhysical and Theoretical ChemistryCrystallizationGlass transitionbusinessCurrent Opinion in Colloid & Interface Science
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Microfluidics and Macromolecules: Top-Down Analytics and Bottom-Up Engineering of Soft Matter at Small Scales

2016

Microfluidics is the art of creating and manipulating small portions of fluids. A typical variant of this art is fluid transport within small channels, either in form of laminar co-flow of miscible streams or in form of segmented-flow dripping and jetting of immiscible streams. Either method provides means to expose components of interest to defined local conditions such as spatially controlled concentration profiles that could not be established without the microfluidic auxiliaries. This ability renders microfluidics uniquely useful as both a method for advanced analytics and synthesis. This article sheds a spotlight on the use and utility of this method in macromolecular chemistry and phy…

Polymers and Plasticsbusiness.industryOrganic ChemistryMicrofluidicsLaminar flowNanotechnology02 engineering and technologyTop-down and bottom-up design010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsFluid transport01 natural sciences0104 chemical sciencesTemplateAnalyticsMaterials ChemistrySoft matterPhysical and Theoretical Chemistry0210 nano-technologybusinessMacromoleculeMacromolecular Chemistry and Physics
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The Formation of Glycerol Oligomers with Two New Types of End Groups in the Presence of a Homogeneous Alkaline Catalyst

2019

The purpose of this work was to synthesize and characterize oligoglycerols with the chains of more than four repeating units. Those oligoglycerols may have some interesting applications, among others, as polyoxyalkylation starters. The glycerol oligomerization process was carried out during 12 h, at 230 &deg

Polymers and PlasticscatalysisElectrospray ionizationmechanismGeneral ChemistryglycerolCarbon-13 NMRArticleCatalysisoligomerizationlcsh:QD241-441chemistry.chemical_compoundchemistrylcsh:Organic chemistryPolymer chemistryGlycerololigoglycerolCarboxylateFourier transform infrared spectroscopySodium carbonatepolyglycerolsBar (unit)Polymers
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Study of the High-Frequency Inductive Coupled Discharge Plasma Interaction with Walls

2007

The high-frequency electrodeless light sources (HFELS) are widely used as bright radiators of narrow and intense spectral lines covering the region from VUV to IR. Special HFELS filled with pure helium at pressures from 0.2 to 5 Torr were prepared for diagnostics of interaction between the filling element and the wall material (glass). Pollution of the discharge plasma with the oxygen admixture was studied by spectroscopy. Atomic force microscopy experiments were performed to find modification of the wall surface at the nanoscale level. Release of oxygen by the walls is found to depend strongly on the discharge conditions and significant changes of the surface structure are detected after p…

Polymers and PlasticschemistryTorrSurface modificationchemistry.chemical_elementPlasmaAtomic physicsCondensed Matter PhysicsSpectroscopyNanoscopic scaleOxygenHeliumSpectral linePlasma Processes and Polymers
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Highly trans-stereospecific Isoprene Polymerization by Neodymium Borohydrido Catalysts

2005

Highly stereospecific polymerization of isoprene was achieved using borohydridoneodymium complexes. In combination with stoichiometric amounts of dialkylmagnesium, Nd(BH4)3(THF)3 (1) and Cp*‘Nd(BH4)2(THF)2 (2) (Cp*‘ = C5Me4nPr) afford very efficient catalysts. The activity reaches 37300 (g of polyisoprene/mol of Nd)/h. Half-lanthanidocene 2 gives rise to polyisoprene, 98.5% trans-regular, the highest content yet described for a homogeneous organometallic catalyst. NMR experiments argue for the formation of bimetallic Nd(μ-BH4)Mg active species.

Polymers and Plasticschemistry.chemical_element010402 general chemistry01 natural sciencesNeodymiumCatalysisInorganic Chemistry[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compoundStereospecificityPolymer chemistryMaterials Chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryBimetallic stripIsoprene010405 organic chemistryChemistryOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciences[ CHIM.POLY ] Chemical Sciences/Polymers[CHIM.POLY]Chemical Sciences/PolymersPolymerizationHomogeneousStoichiometry
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Adduct formation by sub-coordinated metal complexes—VI. Synthesis and pyridine adducts of some nickel(II) chelates formally tri-coordinated

1976

Polymers and Plasticschemistry.chemical_elementAdductMetalchemistry.chemical_compoundNickelchemistryvisual_artPyridinePolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumOrganic chemistryChelationJournal of Inorganic and Nuclear Chemistry
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