Search results for "fourier transform infrared spectroscopy"

showing 10 items of 394 documents

Morphology, mechanical properties and thermal degradation kinetics of PMMA-zirconia nanocomposites prepared by melt compounding

2012

Zirconia nanoparticles were synthesized by means of a sol-gel method and embedded in poly(methyl methacrylate) (PMMA) by melt compounding. The zirconia was well dispersed in the PMMA matrix, with only a few clusters, especially for the highest investigated zirconia content. NMR results showed heteronuclear dipolar interactions involving the carbons and the surrounding hydrogen nuclei. The effect of the amount of zirconia, in the range of 1–5!wt%, on the thermomechanical properties and thermal degradation kinetics of PMMA was also investigated by means of dynamic mechanical analysis (DMA), thermogravimetric analyses (TGA), and Fourier-transform infrared spectroscopy (FTIR). The presenc…

MorphologyThermogravimetric analysisMaterials sciencePolymers and PlasticsGeneral Chemical EngineeringNanoparticleInfrared spectroscopylcsh:Chemical technologyNanocompositeslcsh:TA401-492Materials Chemistrylcsh:TP1-1185Cubic zirconiaThermal stabilityPhysical and Theoretical ChemistryFourier transform infrared spectroscopyComposite materialSettore CHIM/02 - Chimica FisicaNanocompositeOrganic ChemistryDynamic mechanical analysisPMMAnanocomposites PMMA zirconia morphology dynamic mechanical analysis thermal degradationThermal degradationZirconialcsh:Materials of engineering and construction. Mechanics of materialsExpress Polymer Letters
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Efficient Synthesis and X-ray Structure of [1,2,4]Triazolo[4,3-a]pyridines via Oxidative Cyclization Using N-Chlorosuccinimide (NCS)

2021

Triazolopyridines are a family of compounds that, owing to their biological activity, have many pharmaceutical applications. In this study, 3-(pyridine-4-yl)-[1,2,4]triazolo[4,3-a]pyridine and 6-bromo-3-(pyridine-4-yl)-[1,2,4]triazolo[4,3-a]pyridine were synthesized by using the chlorinated agent NCS for hydrazones under very mild conditions. The characterization of these compounds was achieved by 1H NMR, 13C NMR, FTIR, MS and X-ray diffraction. The compound 3-(pyridine-4-yl)-[1,2,4]triazolo[4,3-a]pyridine was crystallized in the monoclinic space group P 21/c with a = 15.1413(12), b = 6.9179(4), c = 13.0938(8) Å, β = 105.102(6)°, V = 1324.16(16)Å3, Z = 4, and R = 0.0337. Also compound 6-bro…

N-ChlorosuccinimideH-bondingcrystal structureCrystallographysynthesisHydrogen bondGeneral Chemical EngineeringCrystal structureCarbon-13 NMRCondensed Matter PhysicsMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundNCSchemistryQD901-999PyridineProton NMRGeneral Materials ScienceFourier transform infrared spectroscopy124-triazolo[43-<i>a</i>]pyridineMonoclinic crystal systemCrystals
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Optimal degradation of Ciprofloxacin in a heterogeneous Fenton-like process using (δ-FeOOH)/MWCNTs nanocomposite

2021

Abstract This study was aimed at the synthesis and characterization of ( δ -FeOOH)/MWCNTs nanocomposite as the catalyst for Ciprofloxacin (CIP) removal through a heterogeneous Fenton-like process. The proposed experimental design applies the central composite design (CCD) as a response surface methodology (RSM). The effect of influential parameters, including initial CIP concentration, catalyst dose, H 2 O2 concentration, initial pH, and reaction time on removal, were investigated. ( δ -FeOOH)/MWCNTs nanocomposite was synthesized using a single-step co-precipitation technique. Besides, nano-feroxyhyte and nanocomposite properties were characterized by transmission electron microscopy (TEM),…

NanocompositeMaterials scienceCentral composite designVDP::Medical disciplines: 700::Clinical medical disciplines: 750Soil ScienceInfrared spectroscopy02 engineering and technologyPlant Science010501 environmental sciences021001 nanoscience & nanotechnology01 natural sciencesCatalysisTransmission electron microscopyResponse surface methodologyAbsorption (chemistry)Fourier transform infrared spectroscopy0210 nano-technology0105 earth and related environmental sciencesGeneral Environmental ScienceNuclear chemistry
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Selective functionalization of halloysite cavity by click reaction: structured filler for enhancing mechanical properties of bionanocomposite films

2014

Selective modification of the inner surface of halloysite nanotubes (HNTs) by the cycloaddition of azides and alkynes (click reaction) was successfully achieved. Fourier transform infrared spectroscopy and thermogravimetry confirmed that the modification involved only the HNT cavity. Morphological investigations evidenced that the functionalized nanotubes formed microfibers and clusters in the micrometer range. By means of the casting method, these nanomaterials were dispersed into biopolymeric matrixes (chitosan and hydroxypropyl cellulose) with the aim of obtaining nanocomposite films with tunable properties from the physicochemical viewpoint. For comparison purposes, we also characterize…

NanocompositeMaterials scienceHydroxypropyl celluloseNanotechnologySettore CHIM/06 - Chimica Organicaengineering.materialHalloysiteSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsNanomaterialsThermogravimetrychemistry.chemical_compoundGeneral EnergychemistryClick chemistryengineeringSurface modificationhalloysite biopolymers click-reactionPhysical and Theoretical ChemistryFourier transform infrared spectroscopySettore CHIM/02 - Chimica Fisica
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Green synthesis and characterizations of silver and gold nanoparticles using leaf extract of Rosa rugosa

2010

Abstract Metal nanostructures have unusual physicochemical properties and biological activities compared to their bulk parent materials. Thus in recent years a number of physical, chemical and biological techniques were applied for the development of metal nanoparticles (NP). Here we have synthesized silver and gold nanoparticles (AgNPs and AuNPs) by using leaves extracts of Rosa rugosa . Surface plasmon resonance spectra for silver and gold are obtained at 451 and 578 nm with brown yellow and pink-red color, respectively. AgNPs and AuNPs vary in size according to different leaves extract and metal concentration used for the synthesis. Different instrumental techniques were applied to chara…

NanostructureChemistryInfrared spectroscopyNanoparticleNanotechnologyMetalColloid and Surface ChemistryTransition metalColloidal goldvisual_artvisual_art.visual_art_mediumFourier transform infrared spectroscopySurface plasmon resonanceNuclear chemistryColloids and Surfaces A: Physicochemical and Engineering Aspects
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FTIR Studies of Silicon Carbide 1D-Nanostructures

2015

Stable 1D silicon carbide nanostructures (nanowires) have been obtained via combustion synthesis route. Infrared absorption and reflection spectra for as-obtained and purified SiC nanowires were compared with the spectra of commercially available SiC nanomaterials. Principal vibrational modes have been identified. Reflectivity spectrum has been reconstructed by modeling of the dielectric function

NanostructureMaterials scienceMechanical EngineeringAnalytical chemistryNanowireInfrared spectroscopyCondensed Matter PhysicsSpectral lineNanomaterialschemistry.chemical_compoundChemical engineeringchemistryMechanics of MaterialsMolecular vibrationSilicon carbideGeneral Materials ScienceFourier transform infrared spectroscopyMaterials Science Forum
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Flow injection Fourier transform infrared determination of nicotine in tobacco

2000

A fully automated procedure is proposed for the Fourier transform infrared (FTIR) determination of nicotine in tobacco. The method is based on the on-line extraction of nicotine with CHCl3. Samples, weighed inside empty extraction cartridges, were humidified with NH3 and the cartridges were installed in a flow manifold in which they were extracted with 2 ml CHCl3 for 2 min, then 400 microliters of the extract were introduced into a micro-flow cell using a carrier of CHCl3 and the IR spectrum was registered continuously. The absorbance, in the wavenumber range 1334-1300 cm-1, was measured, obtaining a peak as a function of time. The area of this peak was interpolated on a calibration line es…

NicotineAnalytical chemistryInfrared spectroscopyStandard solutionBiochemistryAnalytical ChemistryAbsorbanceNicotinesymbols.namesakeTobaccoElectrochemistrymedicineHumansEnvironmental ChemistryFourier transform infrared spectroscopySpectroscopyDetection limitChromatographyFourier AnalysisChemistryExtraction (chemistry)Plants ToxicFourier transformFlow Injection Analysissymbolsmedicine.drugThe Analyst
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Adsorption and photocatalytic degradation of acetonitrile: FT-IR investigation

2003

Abstract The photocatalytic degradation of acetonitrile was carried out in liquid–solid regime in a batch reactor by using two types of commercial TiO 2 powders (Merck and Degussa P25) as photocatalysts. The concentration of acetonitrile and non-purgeable organic carbon (NPOC) were monitored. The initial rate of acetonitrile conversion was found higher on TiO 2 Merck than on TiO 2 P25. FT-IR spectroscopy was used to investigate the molecular features of the adsorption and photo-oxidation of acetonitrile on the two TiO 2 powders in a fully surface hydrated form. Acetonitrile was found adsorbed on Ti 4+ surface ions and hydroxyl groups for both types of TiO 2 . This interaction appeared fully…

NitrileFF-IR investigationProcess Chemistry and TechnologyInorganic chemistryInfrared spectroscopyCatalysisTiO2; acetonitrile; adsorption; photocatalysis; FF-IR investigationTitanium oxideCatalysisacetonitrilechemistry.chemical_compoundAdsorptionchemistryadsorptionPhotocatalysisTiO2Physical and Theoretical ChemistryFourier transform infrared spectroscopyAcetonitrilephotocatalysis
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Structural characterisation and nuclease activity of mixed copper(II) complexes with sulfonamides and bipyridil

2003

Mixed copper complexes have been synthetised through reaction of Cu(II) salts with bipyridil and N-quinolin-8-yl-p-toluenesulfonamide (Hqtsa), N-quinolin-8-yl-benzenesulfonamide (Hqbsa) or N-quinolin-8-yl-naftalenesulfonamide (Hqnsa). Single crystal X-ray diffraction structure determination shows that copper cations are five-coordinated, one complex have distorted bipyramidal trigonal geometry and the other have a distorted square-pyramid. The FT IR and EPR spectra are also reported. Electrophoresis results show that the synthetised complexes in the presence of ascorbate and hydrogen peroxide are chemical nucleases.

NucleasebiologyChemistrychemistry.chemical_elementCopperlaw.inventionInorganic ChemistryElectrophoresisCrystallographychemistry.chemical_compoundBipyramidlawMaterials Chemistrybiology.proteinPhysical and Theoretical ChemistryFourier transform infrared spectroscopyElectron paramagnetic resonanceHydrogen peroxideSingle crystalInorganica Chimica Acta
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A crucial role of adamantanoid Cu(II) complexes in the redox systems: CuCl–diallylsulfoxide–O2 and CuCl2–diallylsulfide–O2

2014

Abstract The hypothetically reversible [Cu(I)(diallylsulfoxide)] ↔ O 2 [Cu(II)(diallylsulfide)] system was examined by FTIR spectroscopy and X-ray diffraction. It is stated that the Cu4OCl6 body centered adamantanoid cages, appearing at both the substrate and product sites, act as a template to promote the oxidation of diallylsulfide to diallylsulfoxide or Cu(I) to Cu(II), thus making the reaction irreversible. Each of these two adamantanoid cores possesses a different point symmetry as well as self assembly mode to form two polymorphs of the [Cu4OCl6(diallylsulfoxide)4] complex. Their polymorphic relationships based on the symmetry homology S4 ← Td → C3, as well as the distortion in the Cu…

O-body centered adamantanoid cagestructural homologyDiallylsulfideChemistryPoint symmetrydiallylsulfide oxidationRedoxpolymorphismInorganic ChemistryStructural homologyCrystallographyPolymorphism (materials science)Materials ChemistrySelf-assemblyPhysical and Theoretical ChemistryFourier transform infrared spectroscopyCoordination geometryPolyhedron
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