Search results for "Pyrolysis"

showing 10 items of 170 documents

Pyrolysis gas chromatography-mass spectrometry in environmental analysis: Focus on organic matter and microplastic

2020

Pyrolysis gas chromatography-mass spectrometry (Py-GC-MS) has great potential within environmental analysis. This technique is mainly used for the chemical identification of macromolecules that cannot be characterized by either liquid or gas chromatography due to their big size. Through pyrolysis (controlled thermal degradation), these macromolecules are broken down into simpler molecules that can be separated by gas chromatography and detected by mass spectrometry. This technique has been traditionally used in environmental samples for the characterization of organic matter and humic substances, contaminants, lignins, etc. It attains the identification of the different types of chemical un…

chemistry.chemical_classificationMicroplasticsCurie-pointEnvironmental analysisEvolved gas analysisChemistry010401 analytical chemistryMass spectrometry01 natural sciences0104 chemical sciencesAnalytical ChemistryFilamentsPyrolysis–gas chromatography–mass spectrometryEnvironmental chemistryReactive pyrolysisOrganic matterEvolved gas analysisGas chromatographyPyrolysisMicrofurnacesSpectroscopy
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Generation and transformation of the [3.3.1]propellane skeleton by thermal rearrangements

1994

Abstract In a sequence of unexpected thermal rearrangements the strained monocyclic alkyne 4 is transformed into the tricyclic system 5 which yields in a flash vacuum pyrolysis again a monocyclic compound 10 .

chemistry.chemical_classificationPropellanechemistry.chemical_compoundFlash vacuum pyrolysischemistryComputational chemistryOrganic ChemistryDrug DiscoveryThermalAlkynePhotochemistryBiochemistryTransformation (music)Tetrahedron Letters
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Thermal Rearrangements of Perchlorohexatrienes-Structures and Experimental and Theoretical Evaluation of Pathways to Isomerization and Cyclization

2009

We have prepared trans- (1) and cis-octachloro-1,3,5-hexatriene (2) by known routes and studied their thermal behavior experimentally and theoretically by ab initio calculations. The three double bonds in 1 and 2 are completely decoupled due to steric hindrance by the eight Cls, as indicated by calculations as well as the single-crystal X-ray structure of 1. The cis isomer 2 can be isomerized to the trans isomer 1 by heating it to 220–250 °C either neat or dissolved in high-boiling solvents, leading to a roughly 2:1 mixture of trans and cis isomers. Calculations at several different levels of theory predict 1 and 2 to be isoenergetic within 2 kJ mol–1. Unimolecular cis/trans isomerization i…

chemistry.chemical_classificationSteric effectsDouble bondFlash vacuum pyrolysisOrganic ChemistryPhotochemistryCis trans isomerizationchemistry.chemical_compoundchemistryOrganic chemistryCyclopentenePhysical and Theoretical ChemistryIsomerizationCis–trans isomerismFulveneEuropean Journal of Organic Chemistry
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Investigation of polymers in the mass spectrometer, 7. Pyrolysis-gas chromatography-mass spectrometry of low molecular and high polymeric sulfanilami…

1975

A number of low molecular, monomeric and polymeric sulfanilamide derivatives, which have found interest as possibly selective antitumour agents, were investigated by pyrolysis-gas chromatography (GC)-mass spectrometry (MS). Thermal degradation mechanisms were studied using also direct polymer pyrolysis in the ion source of the mass spectrometer. Thermal degradation products as well as low molecular weight sulfanilamides and related model compounds were characterized in their fragmentation behaviour by low and high resolution electron impact and field desorption mass spectrometry. Thermal fragments of structural significance were found, and a differentiation of the low and high molecular sul…

chemistry.chemical_classificationSulfanilamidePolymerMass spectrometryIon sourcePyrolysis–gas chromatography–mass spectrometrychemistry.chemical_compoundMonomerchemistryFragmentation (mass spectrometry)Polymer chemistrymedicineElectron ionizationmedicine.drugDie Makromolekulare Chemie
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ChemInform Abstract: Benzoxetes and Benzothietes - Heterocyclic Analogues of Benzocyclobutene

2012

Benzo-condensed four-ring heterocycles, such as benzoxetes 1 and benzothietes 3 represent multi-purpose starting compounds for the preparation of various higher heterocyclic ring systems. The thermal or photochemical valence isomerizations between the benzenoid forms 1,3 and the higher reactive o-quinoid structures 2,4 provide the basis for the synthetic applications. On the other hand, this valence isomerization impedes in particular the generation and storage of 1 because the thermal equilibrium 1 2 is completely on the side of 2. Thus, the number of erroneous or questionable benzoxete structures published to date is surprisingly high. On the contrary, the thermal equilibrium 3 4 is on th…

chemistry.chemical_classificationThermal equilibriumchemistry.chemical_compoundValence (chemistry)Double bondchemistryFlash vacuum pyrolysisComputational chemistryBenzocyclobuteneThermalGeneral MedicineRing (chemistry)IsomerizationChemInform
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The Influence of Biomass Ash on the Migration of Heavy Metals in the Flooded Soil Profile - Model Experiment

2014

Soils that have been exposed to fl ood waters can be heavily polluted by inorganic and organic compounds. They are mainly compounds which appear in dissolved or suspended form fl owing together with heavily laden fl oodwater, as well as compounds created as a result of reactions in the soil profi le, mostly due to anaerobic transformation of organic matter. Heavy metals brought with fl ood waters are absorbed by the soil and also washed out from fl ood sediments by precipitation when the fl ood recedes. This paper presents the results of research on the effects of fertilization with ash from incineration or pyrolysis of biomass on the migration process of heavy metals (Zn, Cu, Cr, Ni, Pb, C…

chemistry.chemical_classificationbiomass ashlcsh:Environmental protectionfungiEnvironmental engineeringfood and beveragesSedimentBiomassGeneral Medicinefloodcomplex mixturesIncinerationSoilchemistryparasitic diseasesSoil waterSoil horizonEnvironmental sciencelcsh:TD169-171.8Organic matterheavy metalsPyrolysisGlebaArchives of Environmental Protection
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An alternative route to 2H-naphtho[1,2-b]thiete and its cycloaddition products

1998

2-(1H-Benzotriazol-1-ylmethyl)-1-naphthalenol (1) can be transformed in high yields to the corresponding thiol 4. Flash vacuum pyrolysis of 4 leads to 2H-naphtho[1,2-b]thiete (5). The benzotriazolyl group proved to be a good leaving group; however, a subsequent nitrogen extrusion takes place under flash vacuum pyrolysis conditions and cyclopentadienecarbonitriles 6a,b are formed by a ring contraction (Scheme 1). Cycloaddition reactions of 5 and dienophiles or heterodienophiles yield the naphtho-condensed sulfur heterocycles 8, 10, 12 and 14 (Scheme 2).

chemistry.chemical_classificationchemistryFlash vacuum pyrolysisOrganic ChemistryThiolLeaving groupchemistry.chemical_elementSulfurMedicinal chemistryNitrogenCycloadditionJournal of Heterocyclic Chemistry
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1979

The thermal degradation behavior of head-to-head (H-H) and head-to-tail (H-T) polystyrenes and poly(vinylcyclohexane)s has been investigated by direct pyrolysis in a mass spectrometer. Both H-H and H-T isomers show only small differences in their initial temperatures of decomposition but remarkably different degradation processes. Whereas H-T polystyrene decomposes in accordance with earlier investigations mainly by a radicalic depolymerization into the monomer and yields only a small amount of dimer and trimer, the H-H polystyrene shows no unzipping and only a statistic degradation into oligomeric styrenes. The formation of stilbene is a diagnostic reaction of H-H polystyrene. The pyrolysi…

chemistry.chemical_classificationchemistry.chemical_compoundMaterials scienceMonomerchemistryDepolymerizationDimerPolymer chemistryBackbone chainTrimerPolymerPolystyrenePyrolysisDie Makromolekulare Chemie
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Direct pyrolysis in the mass spectrometer of aromatic polysulfonates and polythiosulfonates

1978

The thermal degradation mechanism of three aromatic polysulfonates and polythiosulfonates was investigated by direct pyrolysis in the ion source of a mass spectrometer. Thermal degradation reactions were followed directly by this method by detecting the thermal and electron impact induced fragments. The results obtained have provided evidence that sulfur dioxide extrusion from the polymer backbone takes place in these polymers above 300°C. The synthesis and molecular characterization of the polymers studied are reported in the text.

chemistry.chemical_classificationchemistry.chemical_compoundchemistryAnalytical chemistryDegradation (geology)ExtrusionPolymerPhotochemistryMass spectrometryPyrolysisSulfur dioxideElectron ionizationIon sourceJournal of Polymer Science: Polymer Chemistry Edition
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Mass spectrometric investigation of polymers: Thermal degradation of truxillic and truxinic polyamides

1975

The thermal degradation mechanism of four isomeric truxillic and truxinic polyamides were investigated by direct pyrolysis in the ion source of a mass spectrometer. Thermal degradation reactions were followed directly by this method by detecting the thermal and electron impact-induced fragments. The results obtained have shown that the thermal degradation products are sensibly different for the head-to-head (hh) and head-to-tail (ht) polymers and that the predominant pyrolytic process is the cyclobutane ring cleavage. In the hh isomers, both symmetrical and asymmetrical cyclobutane ring cleavage was detected, while in the ht isomers only symmetrical cleavage occurs; this explains the notice…

chemistry.chemical_classificationchemistry.chemical_compoundchemistryThermal stabilityPyrolytic carbonPolymerRing (chemistry)Cleavage (embryo)PhotochemistryMass spectrometryPyrolysisCyclobutaneJournal of Polymer Science: Polymer Chemistry Edition
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