Search results for "Mono"

showing 10 items of 6843 documents

Characterization of commercial synthetic resins by pyrolysis-gas chromatography/mass spectrometry: application to modern art and conservation.

2009

To characterize a set of synthetic resins, a methodology by pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) has been developed. The studied reference materials were commercial versions of a wide range of synthetic resins. For each polymer, the pyrolytic and chromatographic conditions were optimized to adequately resolve the fragment mixture in a short time. The proposed analytical method does not require previous treatment of the sample, and due to its high sensitivity, only a small sample quantity in the microgram range can be used. The pyrolysis temperature was found to have little effect on the obtained pyrograms. The summarized data set for the individual polymer materials, es…

chemistry.chemical_classificationChromatographyChromatographySynthetic resinChemistrySpectrometryChromatographic analysisObjectes d'art--Conservació i restauracióPyrolysis-gasPolymerMass spectrometryAnalytical methodSpectrum analysisAnalytical ChemistryCharacterization (materials science)Anàlisi espectralchemistry.chemical_compoundPyrolysis–gas chromatography–mass spectrometryMonomerArt objects--Conservation and restorationPyrolytic carbonCromatografiaSynthetic resinsModern artPyrolysisAnalytical chemistry
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HPLC in the characterisation of conformational species of linear gramicidins

1997

Abstract High-performance size-exclusion chromatography (HPSEC) has proved to be a highly simplified and rapid procedure to investigate the conformational behaviour of gramicidin A inserted in different model membrane systems (lipid dispersions, liposomes, micelles) based on the separation of double-stranded dimers and monomers present in the lipid assemblies. The HPSEC approach has been extended to the characterisation of acylated analogs of gramicidin (palmitoyl- and oleoyl-derivatives) and a series of peptide analogs where tryptophan residues were chemically modified or replaced by less polar residues (phenylalanine or naphtylalanine) lacking H-bonding ability. The Chromatographic result…

chemistry.chemical_classificationChromatographyDimerTryptophanChemical modificationPeptideBiochemistryAnalytical ChemistryAmino acidAcylationchemistry.chemical_compoundMonomerchemistryGramicidinEnvironmental Chemistrylipids (amino acids peptides and proteins)SpectroscopyAnalytica Chimica Acta
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Development of a semiautomated procedure for the synthesis and evaluation of molecularly imprinted polymers applied to the search for functional mono…

2001

Abstract A previously described scaled-down version of the established monolith procedure, where molecularly imprinted polymers (MIPs) are prepared on the bottom surface of chromatographic vials [Anal. Chem. 71 (1999) 2092] has been here further optimised with respect to its full automation. The protocol results in savings of time and reagents compared to the monolith procedure, allowing ca. 60 polymers (∼50 mg each) to be synthesised in parallel. Both blank and imprinted polymers are then evaluated in situ by equilibrium batch rebinding tests. Each step in the synthesis and evaluation was considered with the aim of achieving an automated method with wide applicability with regards to templ…

chemistry.chemical_classificationChromatographyMolecularly imprinted polymerPolymerBiochemistryDissociation (chemistry)Analytical Chemistrychemistry.chemical_compoundMonomerTemplatechemistryPolymerizationEnvironmental ChemistryMoleculeSelectivitySpectroscopyAnalytica Chimica Acta
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Fast high performance liquid chromatography analysis in lipidomics: Separation of radiolabelled fatty acids and phosphatidylcholine molecular species…

2006

Abstract HPLC procedures using conventional C 18 columns are usually used to separate simple and complex lipid mixtures but these methods of separation remain often laborious and very slow. Here, monolithic columns were successfully applied to separate lipids – radiolabelled fatty acid mixtures and individual phosphatidylcholine (PC) molecular species. For that, isocratic elution was performed using two Chromolith™ Performance RP-18e columns connected in series. Detection was achieved by online measurement of radioactivity for radiolabelled fatty acids and by UV absorbance at 205 nm for PC molecular species. The performances of such silica rods were compared to conventional reverse-phase si…

chemistry.chemical_classificationChromatographyMonolithic HPLC columnElutionAnalytical chemistrySilica columnFatty acidBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryStationary phasePhosphatidylcholineLipidomicsEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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Effect of polystyrene coating on pore, structural and chromatographic properties of silica packings

1990

Abstract A series of mesoporous and macroporous silicas with a mean pore diameter (PD), between 6 and 200 nm were reacted with a copolymer of styrene and vinyl-methyldiethoxysilane. The mass load of coated silicas corresponded to the monolayer capacity of the polymer calculated on the basis of the molecular cross-sectional area, except for the two mesoporous silcias of PD = 6 and 7.5 nm. Depending on the pore size, changes occurred in the specific surface area, as, between the native and the coated product. A comparison of the specific pore volume, νp, of silicas before and after polymer immobilization indicated a major loss of νp for the two mesoporous silicas whereas this effect was much …

chemistry.chemical_classificationChromatographyOrganic ChemistryGeneral MedicinePolymerengineering.materialBiochemistryAnalytical ChemistryStyrenechemistry.chemical_compoundchemistryCoatingSpecific surface areaMonolayerCopolymerengineeringPolystyreneMesoporous materialJournal of Chromatography A
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Structurally bound lipids in peat humic acids

2001

Humic acids from highly decomposed peat were subjected to oxidation with alkaline cupric oxide (CuO) at 170°C (single oxidation). Oxidation products were isolated as three fractions, oxidized humic acids, fulvic acids and lipophilic compounds. Isolated oxidized humic acids were subsequently re-oxidized (sequential oxidation) under the same conditions, and released lipophilic compounds were isolated. Lipids released during single and sequential oxidations were determined using capillary gas chromatography and mass spectrometry. Identified compounds accounted for 3.3 and 0.12 wt.% of humic acid content, respectively. Lipid profiles of lipophilic fractions released during single and sequential…

chemistry.chemical_classificationChromatographyOxideFraction (chemistry)Mass spectrometrycomplex mixturesTerpenoidchemistry.chemical_compoundMonomerchemistryGeochemistry and PetrologyOrganic chemistryHumic acidGas chromatographyAbietaneOrganic Geochemistry
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Interfacial tension between polymer-containing liquids - Predictability and influences of additives

1999

The first part of the contribution deals with the interfacial tension, σ, of phase-separated polymer solutions in single or mixed solvents and of binary polymer blends as a function of the relative distance to the critical temperature of the system, special attention being paid to the possibilities of theoretical prediction. Two methods are discussed in more detail. One is based on a realistic description of the Gibbs energy of mixing as a function of composition, the second correlates σ with the length of the measured tie line. The second part is devoted to another aspect, namely the effects of additives on the interfacial tension between the coexisting phases of demixed polymer solutions …

chemistry.chemical_classificationChromatographyPolymers and PlasticsOrganic ChemistryMixing (process engineering)ThermodynamicsPolymerCondensed Matter PhysicsGibbs free energySurface tensionchemistry.chemical_compoundsymbols.namesakeMonomerchemistryMaterials ChemistryCopolymersymbolsPolymer blendTie lineMacromolecular Symposia
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Direct acid-catalysed mechanical depolymerisation of fibre sludge to reducing sugars using planetary milling

2016

Abstract This study performed a direct solvent-free acid-catalysed mechanical depolymerisation of fibre sludge to reducing sugars which involves one step of acid milling in a planetary mill. The common reported ‘solvent-free’ mechanocatalytic depolymerisation of lignocellulose which includes 1) acid impregnation, 2) vacuum evaporation and 3) mechanocatalytic depolymerisation was also performed as a reference. The major converted monosaccharides were determined by capillary electrophoresis and the results of total reducing sugar (TRS) yields were carried out based on the 3,5-dinitrosalicylic acid (DNS) method. The results showed that the TRS conversion of direct acid-catalysed mechanical dep…

chemistry.chemical_classificationChromatographyRenewable Energy Sustainability and the EnvironmentChemistry020209 energyForestryOne-Step02 engineering and technologyCatalysisReducing sugarHydrolysisCapillary electrophoresisChemical engineering[CHIM.ANAL]Chemical Sciences/Analytical chemistryYield (chemistry)0202 electrical engineering electronic engineering information engineeringMonosaccharideWaste Management and DisposalAgronomy and Crop ScienceBall millComputingMilieux_MISCELLANEOUS
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Characterization of totally chlorine-free effluents from Kraft pulp bleaching

1999

A capillary zone electrophoresis (CZE) method for analyzing the total acid hydrolysis products (monosaccharides and their derivatives) of the dissolved carbohydrates from a totally chlorine-free bleaching plant was developed. Several borate buffer concentrations and other running conditions were tested. Neutral monosaccharides (arabinose, galactose, glucose, mannose, rhamnose and xylose) in hydrolysates were derivatized by means of 4-aminobenzonitrile and resolved by 500 mM borate buffer (pH 9.5, 16.0 kV). The detection level was less than 10 fmol. In addition, the separation of some uronic acids and oligosaccharides was studied.

chemistry.chemical_classificationChromatographyRhamnoseOrganic ChemistryGeneral MedicineUronic acidXyloseBiochemistryAnalytical Chemistrychemistry.chemical_compoundHydrolysisCapillary electrophoresisKraft processchemistryMonosaccharideAcid hydrolysisJournal of Chromatography A
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t-Curves for n-Hexane

1992

The adsorption and desorption isotherms of n-hexane on powdered alumina and silica have been studied at 25°C over a wide range of relative pressures. Two t-curves for pore structure analysis are proposed, one for alumina (C = 12) and the second for silica (3 ≤ C ≤ 9). The statistical thickness t of the adsorbed n-hexane layer has been drawn as a function of the relative pressure assuming a maximal thickness of 0.55 nm and a mean thickness of 0.42 nm for the monolayer. The results are discussed in relation to previous published data.

chemistry.chemical_classificationChromatographyStructure analysisGeneral Chemical Engineeringlcsh:QD450-801Analytical chemistrylcsh:Physical and theoretical chemistry02 engineering and technologySurfaces and InterfacesGeneral Chemistry010501 environmental sciences01 natural sciencesHexanechemistry.chemical_compoundAdsorptionHydrocarbon020401 chemical engineeringchemistryDesorptionMonolayerRelative pressure0204 chemical engineeringLayer (electronics)0105 earth and related environmental sciencesAdsorption Science & Technology
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