Search results for " Infrared"

showing 10 items of 945 documents

A Study by Spectroelectrochemical FTIR and Density Functional Theory Calculations of the Reversible Complexing Ability of an Electroactive Tetrathiaf…

2006

We report on the study of the electrochemically targeted complexation/expulsion of a metal cation (Ba2+) by a crown ether tetra(thiomethyl)tetrathiafulvalene derivative (crown-TTM-TTF). Real time, in situ FTIR spectroelectrochemistry was used to obtain spectroscopic evidence of this electrochemically triggered phenomenon. Density functional theory calculations allowed the spectral information collected to be assigned. Both experimental and theoretical results clearly show that neutral crown-TTM-TTF complexes well Ba2+. Complexation is evidenced by a significant downshift of the frequency corresponding to the asymmetric stretching of the C-O-C ether groups. Concerning the cation crown-TTM-TT…

chemistry.chemical_classificationInorganic chemistryEther02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistry01 natural sciences0104 chemical sciencesDicationchemistry.chemical_compoundchemistryPhysical chemistryDensity functional theoryPhysical and Theoretical ChemistryFourier transform infrared spectroscopy0210 nano-technologyDerivative (chemistry)Crown etherTetrathiafulvaleneThe Journal of Physical Chemistry A
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Covalently bonded layer-by-layer assembly of multifunctional thin films based on activated esters.

2009

We demonstrate that chemically stable, multifunctional polymer thin films can be obtained using the layer-by-layer (LbL) deposition based on covalent bonds between adsorbing chains. Poly(pentafluorophenyl-4-vinylbenzoate) (P1) or poly(pentafluorophenylacrylate) (P2) polymers were assembled with poly(allyl amine) (PAAm) to yield LbL multilayer films through amide bond formation by the reaction between activated esters of P1 or P2 and amine groups in PAAm, which was quantitatively monitored by Fourier transform infrared spectroscopy (FT-IR). It was found that the difference in the solubility of P1 and P2 against ethanol, which was used as the solvent for PAAm, during the LbL deposition yields…

chemistry.chemical_classificationLayer by layerInfrared spectroscopySurfaces and InterfacesPolymerSulfonic acidCondensed Matter PhysicschemistryCovalent bondPolymer chemistryElectrochemistrySurface modificationGeneral Materials ScienceAmine gas treatingFourier transform infrared spectroscopySpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Rapid evaluation of oxidised fatty acid concentration in virgin olive oil using Fourier-transform infrared spectroscopy and multiple linear regression

2011

Abstract Fourier-transform infrared spectroscopy (FTIR), followed by multivariate treatment of spectral data, was used to evaluate the oxidised fatty acid (OFA) concentration in virgin olive oil samples characterised by different oxidative status. The entire FTIR spectra (4000–700 cm−1) of oils were divided in 25 wavelength regions. The normalised absorbances of the peak areas within these regions were used as predictors. In order to predict the OFA concentration, multiple linear regression (MLR) models were performed. After a cube root transformation of data, an MLR model constructed using eight predictors was able to predict OFA concentration with an average error of 17%. The main wavelen…

chemistry.chemical_classificationMULTIPLE LINEAR REGRESSIONOXIDATIVE STATUSAnalytical chemistryFatty acidInfrared spectroscopyGeneral MedicineVIRGIN OLIVE OILFOURIER-TRANSFORM INFRARED SPECTROSCOPYAnalytical ChemistryWavelengthsymbols.namesakeOXIDISED FATTY ACIDSVegetable oilFourier transformchemistryLinear regressionsymbolsFourier transform infrared spectroscopyFood ScienceOlive oil
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Dye-containing S∗cside-on/end-on copolymers

1995

Abstract Mesomorphic copolysiloxanes, which combine ‘normal’ end-on linked chiral mesogenic units inducing S∗c phases and side-on fixed chromophores were prepared. The interplay of the different orientational tendencies of these moieties, which are perpendicular (end-on linked mesogenic groups) or parallel (side-on fixed chromophores) to the polymer chain, lead to a strong destabilization of the S∗c phase. However, copolymers with up to about 10 mol % of chromophores still show a smectic C∗ phase. FTIR measurements show that both moieties orient parallel to each other and perpendicular to the polymer chains. These copolymers are interesting to consider as coloured guest-host S∗c materials f…

chemistry.chemical_classificationMaterials scienceMesogenGeneral ChemistryPolymerChromophoreCondensed Matter PhysicsCrystallographychemistryLiquid crystalPhase (matter)CopolymerPerpendicularOrganic chemistryGeneral Materials ScienceFourier transform infrared spectroscopyLiquid Crystals
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Covalently attached polymer mono- and multilayers on silanized glass substrates

1996

Abstract Applying grazing incidence FTIR and ellipsometry, the reaction of poly [(1-methyl-vinyl isocyanate)-alt-(maleic anhydride)](IAP) with amino-silanized glass and silicon oxide surfaces has been investigated. A reactive surface containing isocyanate and anhydride groups was formed after the adsorption of the polymer. The layer could be further functionalized using 2-aminoethanol. Multilayers could be built up by adsorbing a second layer of IAP onto an already reacted first layer of IAP.

chemistry.chemical_classificationMaterials scienceMetals and AlloysMaleic anhydrideSurfaces and InterfacesPolymerIsocyanateSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundAdsorptionchemistrySilanizationPolymer chemistryMaterials ChemistryFourier transform infrared spectroscopySilicon oxideLayer (electronics)Thin Solid Films
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Superhydrophobic TiO2/Fluorinated Polysiloxane Hybrid Coatings with Controlled Morphology for Solar Photocatalysis

2021

Abstract Technological applications of polysiloxane coatings have been influenced by their intrinsic low surface energy, which increases their water repellence. Accurate control of composition and interfacial properties through the introduction of perfluorinated moieties further lowers the polysiloxane surface energy, while mixing with metal oxide nanoparticles enhances roughness, resulting in a great potential in the development of superhydrophobic materials for photocatalysis. Herein, a series of hydrophobic and superhydrophobic hybrid coatings were prepared by dehydrocoupling and hydrosilylation reactions of polymethylhydrosiloxane with 1H,1H,2H,2H‐perfluorooctyltriethoxysilane and 1,3-d…

chemistry.chemical_classificationMaterials sciencePolymethylhydrosiloxaneHydrosilylationtitanium dioxidePMHSPolymerSurface energyContact anglechemistry.chemical_compoundColloid and Surface Chemistryhybrid coatingschemistryChemical engineeringPhotocatalysisfluorinated polysiloxanesWettingFourier transform infrared spectroscopyphotocatalysissuperhydrophobicitySettore CHIM/02 - Chimica Fisica
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Barrier, structural and mechanical properties of bovine gelatin-chitosan blend films related to biopolymer interactions

2014

BACKGROUND The increased use of synthetic packaging films has led to a high ecological problem due to their total non-biodegradability. Thus, there is a vital need to develop renewable and environmentally friendly bio-based polymeric materials. Films and coatings made from polysaccharide polymers, particularly chitosans and gelatins have good gas barrier properties and are envisaged more and more for applications in the biomedical and food fields, as well as for packaging. In this study a casting method was used to develop an edible plasticised film from chitosan and gelatin. Aiming to develop a blend film with enhanced properties, the effects of mixing chitosan (CS) and gelatin (G) in diff…

chemistry.chemical_classificationNutrition and Dieteticsfood.ingredientMaterials sciencePolymerengineering.materialGelatinChitosanchemistry.chemical_compoundOxygen permeabilityfoodchemistryChemical engineeringPolymer chemistryUltimate tensile strengthengineeringBiopolymerFourier transform infrared spectroscopySolubilityAgronomy and Crop ScienceFood ScienceBiotechnologyJournal of the Science of Food and Agriculture
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Photosensitive functionalized surface-modified quantum dots for polymeric structures via two-photon-initiated polymerization technique.

2015

In this paper, the surface modification of CdSe- and CdZnS-based quantum dots (QDs) with a functional silica shell is reported. Functionalized silica shells are prepared by two routes: either by ligand exchange and a modified Stober process or by a miniemulsion process with amphiphilic poly(oxyethylene) nonylphenylether also know as Igepal CO-520 (IG) as oligomeric amphiphile and modified silica precursors. The polymerizable groups on the functionalized silica shell allow covalent bonding to a polymer matrix and prevent demixing during polymerization and crosslinking. This allows the homogeneous incorporation of QDs in a crosslinked polymer matrix. This paper furthermore demonstrates that t…

chemistry.chemical_classificationPhotonsMaterials sciencePolymers and PlasticsPolymersSurface PropertiesOrganic ChemistryPolymerSilicon DioxidePolymerizationMiniemulsionchemistryPolymerizationChemical engineeringQuantum dotCovalent bondAmphiphileStöber processPolymer chemistryQuantum DotsSpectroscopy Fourier Transform InfraredMaterials ChemistrySurface modificationMacromolecular rapid communications
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FT-IR and dielectric study of water/AOT liquid crystals

2000

Abstract In order to explore the influence of microwave radiation on highly viscous microheterogeneous systems, the evolution of structural and dynamical properties of the water/sodium bis(2-ethylhexyl) sulfosuccinate (AOT) liquid crystals as a function of the molar ratio R (R=[water]/[AOT]) has been investigated by FT-IR spectroscopy and time domain reflectometry. The study emphasises how the progressive hydration of the surfactant head groups is mainly responsible for the structural and dynamical evolution of water/AOT liquid crystals. In particular, it has been found that the state of water at lower R values is strongly perturbed, bulk-like water appears only at R>23 and the water/AOT in…

chemistry.chemical_classificationSodiumOrganic ChemistryAnalytical chemistryIonic bondingchemistry.chemical_elementDielectricAnalytical ChemistryInorganic ChemistrychemistryPulmonary surfactantLiquid crystalCounterionFourier transform infrared spectroscopySpectroscopySpectroscopyJournal of Molecular Structure
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ChemInform Abstract: In situ DRIFT Spectroscopic Investigation on the Chemical Evolution of Zinc Phosphate Acid-Base Cement.

2010

Diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy has been used to follow the chemical evolution of zinc phosphate acid−base cement (ZPC), which has been prepared from unmodified, as well as from aluminum- and zinc-modified orthophosphoric acid. For the first time, amorphous dizinc cyclotetraphosphate octahydrate, Zn2P4O12·8H2O, although hydrolytically instable, has been observed as precursor phase prior to crystallization of α-hopeite, α-Zn3(PO4)2·4H2O, in both systems. Within minutes from onset of mixing the infrared spectrum of unmodified ZPC is dominated by the characteristic vibrations of α-hopeite, due to matrix crystallization. Setting of modified ZPC is strongly af…

chemistry.chemical_classificationSteric effectsDiffuse reflectance infrared fourier transformBase (chemistry)ChemistryInorganic chemistryZinc phosphateGeneral Medicinelaw.inventionAmorphous solidchemistry.chemical_compoundlawPhase (matter)CrystallizationSpectroscopyChemInform
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