Search results for "absorption"

showing 10 items of 2701 documents

High-energy radiation processing, a smart approach to obtain PVP-graft-AA nanogels

2014

Abstract Poly(N-vinylpyrrolidone)-grafted-acrylic acid biocompatible nanogels (NGs) were prepared using an exiting industrial-type electron accelerator and setups, starting from semi-dilute aqueous solutions of a commercial PVP and the acrylic acid monomer. As a result, NGs with tunable size and structure can be obtained quantitatively. Sterility was also imparted at the integrated dose absorbed. The chemical structure of the NGs produced was confirmed through Fourier Transformer Infrared Spectroscopy (FT-IR). The molecular and physico-chemical properties of NGs, such as the hydrodynamic dimensions and surface charge densities, for various polymer and monomer concentrations in the irradiate…

chemistry.chemical_classificationPoly(N-vinylpyrrolidone) Acrylic acid grafting Nanogels E-beam irradiationRadiationMaterials scienceAqueous solutionAbsorption spectroscopyInfrared spectroscopyPolymerchemistry.chemical_compoundMonomerchemistryChemical engineeringPolymer chemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologieSurface chargeSpectroscopyPoly(N-vinylpyrrolidone); acrylic acid grafting; nanogels; e-beam irradiation.Acrylic acidRadiation Physics and Chemistry
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1997

On the basis of an extended series of monodisperse oligomers of the dialkoxy-substituted phenyleneethenylenes 1a–i the Eqs. (3) and (4) were conceived in order to determine the limiting values of the energies Ei and the wavelengths λi of the UV/vis absorption. The convergence of the Ei, and λi values with a growing number n of repeating units permits a precise prediction of the Ei,∞ and λi,∞ values of the corresponding polymer 1j as well as a statement about the overall effect of conjugation ΔEi and the effective conjugation length ECL. A great variety of different conjugated oligomers 2–14 can be evaluated by the same algorithm.

chemistry.chemical_classificationPolymers and PlasticsSeries (mathematics)Absorption spectroscopyGeneral Chemical EngineeringDispersityPolymerConjugated systemSpectral lineUltraviolet visible spectroscopychemistryPolymer chemistryPhysical chemistryAbsorption (electromagnetic radiation)Acta Polymerica
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Crown ethers derived from bicyclocalix[4]arenes as chromoionophores

2001

The synthesis of calix[4]arenes in which opposite phenolic units are connected by a poly(oxyethylene) bridge at the narrow rim and a 2,6-dimethylene-4-nitrophenol bridge at the wide rim is reported. For two derivatives with tetra- (4) and penta(oxyethylene) (5) bridges UV-Vis spectrophotometric studies were carried out in buffered solution in the presence of alkali metal ions. Their complexation was associated with changes in their UV-Vis spectra, especially with an increase of the absorption band at 450 nm. For 4 and 5 this was most intense in the presence of potassium and caesium ions, respectively, indicating that the calixarene with the shorter crown ether bridge is selective towards po…

chemistry.chemical_classificationPotassiumchemistry.chemical_elementGeneral ChemistryAlkali metalCatalysisIonchemistry.chemical_compoundchemistryAbsorption bandCaesiumPolymer chemistryCalixareneMaterials ChemistryOrganic chemistryPhenolCrown etherNew Journal of Chemistry
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Effects of isoflurane on the Dnase I activity in an isolated enzyme preparation and on the Dnase I-G actin complex

1991

Effects of isoflurane on the DNase I activity in an isolated enzyme preparation and in the DNase I-globular (G) actin complex were investigated. DNase I, DNase I-G actin complex, and G actin were exposed to various (0.2–4.0 vol%) isoflurane concentrations for 180 min. Thereafter, DNase I activity was determined. DNase I activity was inhibited in relation to time and concentration of isoflurane exposure. At concentrations ranging from 0.2 to 1.0 vol% of isoflurane inactive DNase I was activated in the DNase I-G actin complex. The DNase I inhibitor G actin showed a reduced capability to inhibit DNase I following isoflurane exposure. Albumin can inhibit the DNase I inactivation possibly by com…

chemistry.chemical_classificationProtein DenaturationIsofluraneAlbuminAbsorption (skin)BuffersToxicologyMolecular biologyActinschemistry.chemical_compoundEnzymechemistryBiochemistryIsofluranemedicineAnimalsDeoxyribonuclease ICattlePancreasDNAActinDNA Damagemedicine.drugJournal of Biochemical Toxicology
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Polymer absorption in dense polymer brushes vs. polymer adsorption on the brush-solvent interface

2014

Molecular-dynamics simulations of a coarse-grained model of a dense brush of flexible polymers (of type A) interacting with a long flexible macromolecule (of type B) are presented, considering the case of an attractive AB interaction, while effective interactions between AA and BB pairs of monomers are repulsive. Varying the strength of the attraction between unlike monomers, an adsorption transition at some critical value is found, where the B-chain is bound to the brush-solvent interface, similar to the adsorption on a planar solid substrate. However, when is much higher than , the long macromolecule is gradually “sucked in” the brush, developing many pieces that are locally stretched in …

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceRelaxation (NMR)General Physics and AstronomyPolymerPolymer adsorptionCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundReptationMonomerAdsorptionchemistryChemical physicsAbsorption (chemistry)MacromoleculeEPL (Europhysics Letters)
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Antimicrobial activity of methylene blue and toluidine blue O covalently bound to a modified silicone polymer surface

2009

Methylene Blue or Toluidine Blue O were covalently bound to an activated silicone polymer by means of an amide condensation reaction. UV-visible absorption spectra confirmed that the dye was surface bound. The new polymers with covalently attached dye display significant bactericidal activity against Escherichia coli and Staphylococcus epidermidis with a 99.999% reduction in viable bacteria after four minutes exposure to a low power laser.

chemistry.chemical_classificationRMAbsorption spectroscopybiologyGeneral ChemistryPolymerPhotochemistrybiology.organism_classificationCondensation reactionmedicine.disease_causeRSchemistry.chemical_compoundchemistryCovalent bondStaphylococcus epidermidisAmidePolymer chemistryMaterials ChemistrymedicineEscherichia coliMethylene blueJournal of Materials Chemistry
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Unexpectedly ambivalent O-2 role in the autocatalytic photooxidation of 2-methoxybenzyl alcohol in water

2015

An unusual autocatalytic photooxidation of 2-methoxybenzyl alcohol has been observed under UV irradiation in aqueous medium. The homogeneous oxidation is catalyzed by the corresponding aldehyde that is also the main oxidation product. The trend of alcohol disappearance rate matches the typical shape of an autocatalytic process, where a crucial and ambivalent role is played by the presence of molecular oxygen. Low oxygen concentrations give rise to a zero-order reaction since the beginning of irradiation, while higher amounts of oxygen reduce the alcohol oxidation rate until the aldehyde reaches a concentration high enough to speed up the alcohol's conversion. Experiments performed by varyin…

chemistry.chemical_classificationSettore ING-IND/24 - Principi Di Ingegneria ChimicaAqueous solutionAutocatalytic photooxidation 2-Methoxybenzyl alcohol 2-Methoxybenzaldehyd O2 quenchingHomogeneous photocatalysisProcess Chemistry and Technologychemistry.chemical_elementAlcoholSettore CHIM/06 - Chimica OrganicaPhotochemistryOxygenAldehydeCatalysisCatalysisAutocatalysischemistry.chemical_compoundchemistrySettore CHIM/03 - Chimica Generale E InorganicaAlcohol oxidationPhysical and Theoretical ChemistryAbsorption (chemistry)
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Chemistry of Desiccant Properties of Carbohydrate Polymers as Studied by Near-Infrared Spectroscopy

2013

Published version of an article in the journal: Industrial and Engineering Chemistry Research. Also available from the publisher at: http://dx.doi.org/10.1021/ie302199k The combination frequency of water molecule in near-infrared spectroscopy is very useful for studying water molecular adsorption on solid surfaces. The absorption is purely from water molecules, and the variation in the absorption bands reflects the change in the environment of the water molecules on a surface. This variation, in turn, reflects the nature of the functional groups on the surface. Recently, Christy used this information in combination with second-derivative techniques to probe the surface of hydrothermally tre…

chemistry.chemical_classificationSilica gelGeneral Chemical EngineeringGeneral ChemistryPolymerVDP::Teknologi: 500::Kjemisk teknologi: 560Industrial and Manufacturing Engineeringchemistry.chemical_compoundAdsorptionChemical engineeringchemistryVDP::Matematikk og Naturvitenskap: 400::Kjemi: 440AmyloseAmylopectinPolymer chemistryMoleculeAbsorption (chemistry)SpectroscopyIndustrial & Engineering Chemistry Research
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Star-Shaped Compounds Having 1,3,5-Triazine Cores

2003

The 1,3,5-triazine derivatives 1−4 having styryl or higher oligo(phenylenevinylene) chains in the 2-, 4-, and 6-positions represent star-shaped push-pull compounds. Alkoxy or dimethylamino groups on the peripheral benzene rings, which act as electron donors, and the central 1,3,5-triazine ring, which acts as an electron acceptor, cause intramolecular charge transfer (ICT) to occur in the absorption S0⇄S1. Protonation of the 1,3,5-triazine core enhances the effect, as demonstrated by a bathochromic shift; a secondary protonation on the dimethylamino groups, however, leads to the breakdown of the ICT. Thus, the yellow compound 1d first becomes violet and then colorless upon the addition of tr…

chemistry.chemical_classificationStereochemistryChemistryOrganic ChemistryProtonationElectron acceptorMedicinal chemistrychemistry.chemical_compound135-TriazineIntramolecular forceBathochromic shiftAlkoxy groupTrifluoroacetic acidPhysical and Theoretical ChemistryAbsorption (chemistry)European Journal of Organic Chemistry
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Mono and dinuclear copper(II) complexes of 2,4,6-tris(2-pyridyl)-1, 3,5-triazine and halide or pseudohalide ions: Synthesis and spectral studies

1986

By inhibiting the copper(II) assisted TPT (TPT = 2,4,6-tris(2-pyridyl)-1,3,5-triazine) hydrolysis, monomeric and dimeric copper(II) complexes having as general formulae Cu(TPT)X, · nH2O (X = Cl, Br, NCS, NCO or N3) and [Cu(TPT)X]2(PF6)2 · nH2O (X = Cl, Br, NCS or N3) have been synthesized and characterized by i.r., electronic and e.p.r. spectra, x-ray powder diffraction and analytical data. Spectroscopic results indicate five-coordinate geometry around the copper(II) ion, intermediate between trigonal-bipyramid and square-pyramid structures. The half-field absorption in the ΔMS = 2 region of powdered X-band e.p.r. spectra has been observed for the dimeric species.

chemistry.chemical_classificationStereochemistryMetals and AlloysHalidechemistry.chemical_elementCopperInorganic Chemistrychemistry.chemical_compoundCrystallographyMonomerchemistry135-TriazineMaterials ChemistryAbsorption (chemistry)Inorganic compoundOrganometallic chemistryPowder diffractionTransition Metal Chemistry
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