Search results for " pyrolysis"

showing 10 items of 49 documents

Theoretical determination of the geometric and electronic structures of oligorylenes and poli(peri‐naphthalene)

1992

We present a theoretical investigation of the electronic structure of oligorylenes (from perylene to heptarylene, including also the naphthalene molecule) and their corresponding polymer poly(peri‐naphthalene) (PPN) using the nonempirical valence effective (VEH) method. The geometry of the unit cell used to generate the polymer is extrapolated from the PM3‐optimized molecular geometries of the longest oligorylenes. That geometry shows some bond alternation along the perimeter carbon chains and a bond length of ≊1.46 Å is calculated for the peri bonds connecting the naphthalene units. The VEH one‐electron energy level distributions calculated for oligorylenes are used to interpret the experi…

OptimizationChemical BondsBand gapStereochemistryExtrapolationElectric ConductorsGeometryGeneral Physics and AstronomyElectronic structureMolecular physicsEnergy LevelsMolecular orbitalPhysical and Theoretical ChemistryBand Structure:FÍSICA::Química física [UNESCO]Electronic band structurePeryleneFilmsValence (chemistry)Organic PolymersChemistryElectronic Structure ; Perylene ; Naphthalene ; Organic Polymers ; Unit Cell ; Geometry ; Extrapolation ; Optimization ; Chemical Bonds ; Carbon ; Chains ; Energy Levels ; Ionization Potential ; Affinity ; Band Structure ; Electric Conductors ; Films ; PyrolysisUnit CellChainsCarbonUNESCO::FÍSICA::Química físicaBond lengthIonization PotentialMolecular geometryElectronic StructureAffinityIonization energyNaphthalenePyrolysis
researchProduct

1973

The thermal degradation of poly(oxycarbonylethylene) (poly-β-propiolactone) has been investigated within a temperature range of 180–220°C and under various pressures. The degradation begins with a considerable decrease in molecular weight, followed by an accelerating formation of acrylic acid. The reaction involves the following steps: 1 Random chain scission of polymer chains by typical ester pyrolysis with the formation of fragments one of which containing a carboxylic group the other one a CC-double bond at the chain end (Eq. (1)). 2 Formation of the volatile acrylic acid by scissions at the chain end, the amount of acrylic acid or the weight-loss increasing with the number of fragmentat…

Polyesterchemistry.chemical_classificationchemistry.chemical_compoundChain scissionChemistryCarboxylic groupPolymer chemistryDegradation (geology)β-propiolactonePolymerEster pyrolysisAcrylic acidDie Makromolekulare Chemie
researchProduct

Sensing properties of ZnO nanostructured layers

2017

Nanostructured ZnO layers have been deposited onto SiO 2 /Si substrates by spray pyrolysis, with previously patterned interdigitated gold electrodes. We have then measured the capacitive and resistive response against ambient parameters such as relative humidity and illumination.

Resistive touchscreenMaterials scienceCapacitive sensingHumiditychemistry.chemical_elementZincCapacitanceSpray pyrolysisSemiconductorschemistryElectrodeElectronic engineeringRelative humidityMaterials nanoestructuratsComposite material2017 Spanish Conference on Electron Devices (CDE)
researchProduct

Identification and Evaluation of Hazardous Pyrolysates in Bio-Based Rigid Polyurethane-Polyisocyanurate Foam Smoke

2021

In this study, rigid polyurethane (PU) and polyisocyanurate (PIR) foam samples made from renewable material (tall oil fatty acid) based polyols were analyzed by pyrolysis gas chromatography mass spectrometry (Py-GC/MS) to obtain information about the full relative smoke content, with a focus on substance identification by their functional groups and hazardousness. The relative content of gaseous products produced during the thermal degradation was evaluated between the two samples, differenced by their assigned isocyanate (NCO) index value—150 and 300. The main thermal degradation components of the rigid PU-PIR foam were found to originate from the decomposition of isocyanate, primarily for…

Smokebusiness.product_categoryPolymers and Plasticsanalytical pyrolysisenvironmental hazardsTall oilPolyisocyanurateOrganic chemistryGeneral ChemistryIsocyanateDecompositionrigid PU-PIR foam; analytical pyrolysis; physical hazards; health hazards; environmental hazardsArticlechemistry.chemical_compoundPyrolysis–gas chromatography–mass spectrometryQD241-441Anilinechemistryhealth hazardsrigid PU-PIR foamphysical hazardsOrganic chemistrybusinessPolyurethanePolymers
researchProduct

Slow Pyrolysis as a Method for Biochar Production from Carob Waste: Process Investigation and Products’ Characterization

2021

The zero-waste city challenge of the modern society is inevitably addressed to the development of model’s waste-to-energy. In this work, carob waste, largely used in the agro-industrial sector for sugar extraction or locust beangum (LBG) production, is considered as feedstock for the slow pyrolysis process. According to the Food and Agriculture Organization of the United Nations (FAO), in 2012, the world production of carobs was ca. 160,000 tons, mainly concentrated in the Mediterranean area (Spain, Italy, Morocco, Portugal, and Greece). To evaluate the biomass composition, at first, the carob waste was subjected to thermo-gravimetric analysis. The high content of fixed carbon suggest…

TechnologyControl and OptimizationBiochar Carob waste Slow pyrolysisRenewable Energy Sustainability and the EnvironmentSettore ING-IND/25 - Impianti ChimiciTEnergy Engineering and Power Technologyslow pyrolysisSettore ING-IND/22 - Scienza E Tecnologia Dei Materialicarob wastebiocharElectrical and Electronic EngineeringEngineering (miscellaneous)slow pyrolysis; carob waste; biocharEnergy (miscellaneous)Energies; Volume 14; Issue 24; Pages: 8457
researchProduct

The effect of feedstock origin and temperature on the structure and reactivity of char from pyrolysis at 1300–2800 °C

2018

This study reports the effect of feedstock origin, residence time, and heat treatment temperature on CO2 and O2 reactivities, nanostructure and carbon chemistry of chars prepared at 1300, 1600, 2400, and 2800 °C in a slow pyrolysis reactor. The structure of char was characterized by transmission electron microscopy and Raman spectroscopy. The CO2 and O2 reactivity of char was investigated by thermogravimetric analysis. Results showed that the ash composition and residence time influence the char reactivity less than the heat treatment temperature. The heat treatment temperature and co-pyrolysis of pinewood char with biooil decreased the CO2 reactivity, approaching that of metallurgical coke…

Thermogravimetric analysisBiooilHigh-temperature pyrolysis020209 energyGeneral Chemical EngineeringEnergy Engineering and Power Technologychemistry.chemical_element02 engineering and technologyRaw materialsymbols.namesake020401 chemical engineeringMaschinenbau0202 electrical engineering electronic engineering information engineeringReactivity (chemistry)Char0204 chemical engineeringOrganic ChemistryReactivityMetallurgical cokeFuel TechnologychemistryChemical engineeringTransmission electron microscopyBiomass charsymbolsRaman spectroscopyCarbonPyrolysis
researchProduct

Characterization and reactivity of charcoal from high temperature pyrolysis (800-1600°C)

2019

This study presents the effect of wood origin and heat treatment temperature on the CO2 reactivity, nanostructure and carbon chemistry of chars prepared at 800, 1200, and 1600 °C in slow pyrolysis reactors. The structure of charcoal was characterized by transmission electron microscopy, Raman spectroscopy, mercury intrusion porosimetry and N2 adsorption. The CO2 reactivity of char was investigated by thermogravimetric analysis. Results showed that spruce and oak chars have similar reactivity at all heat treatment temperatures. The oak char prepared at 1600 °C contained long and flat graphene layers and interplanar distance that is similar to graphite and thus, was more ordered t…

Thermogravimetric analysisMaterials science020209 energyGeneral Chemical EngineeringChemieEnergy Engineering and Power Technologychemistry.chemical_element02 engineering and technologyAdsorption020401 chemical engineering0202 electrical engineering electronic engineering information engineeringReactivity (chemistry)CharGraphite0204 chemical engineeringCharcoallow heating rateOrganic Chemistrynon-graphitizing carbonCO2 reactivityFuel TechnologyChemical engineeringchemistryhigh-temperature pyrolysisvisual_artvisual_art.visual_art_mediumPyrolysisCarboncharcoal
researchProduct

Comparative study of historical woods from XIX century by thermogravimetry coupled with FTIR spectroscopy

2019

Thermal and structural properties of historical woods from apparatuses of the Historical Collection of the Physics Instruments of the University of Palermo have been investigated by FTIR spectroscopy coupled with thermogravimetric analysis. Specifically, the wooden portions of apparatuses from XIX century have been studied. The investigated woods belong to different taxa (Swietenia mahagoni, Picea abies and Juglans regia). The thermal behavior of the wooden materials has been successfully interpreted on the basis of specific indexes determined by the quantitative analysis of the FTIR spectra. The kinetics of the wood pyrolysis have been investigated by using a non-isothermal approach based …

Thermogravimetric analysisNon isothermal thermogravimetric analysiPolymers and PlasticsbiologyHistorical woodWood pyrolysisAnalytical chemistryPicea abies02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologybiology.organism_classification01 natural sciences0104 chemical sciencesThermogravimetryFtir spectraFTIR spectroscopyThermogravimetryFourier transform infrared spectroscopy0210 nano-technologySwietenia mahagoniSettore CHIM/02 - Chimica FisicaCellulose
researchProduct

1H-naphtho[2,1-b]thiete and 2H-naphtho[2,3-b]thiete- synthesis and reactivity

1994

Abstract The title compounds 4 and 8 are obtained by flash vacuum pyrolysis of the corresponding hydroxymethylthionaphthols 3 and 7. Whereas 4 shows a smooth ring opening on heating, 8 is thermally stable but reacts photochemically. The different behavior is explained on the basis of an MNDO calculation. The valence isomers 4′ and 8′ represent thioquinonemethides, which are highly reactive components in [12π + 2π]cycloaddition processes (4 → 9, 10, 11; 8 → 12).

Valence (chemistry)Flash vacuum pyrolysisChemistryStereochemistryOrganic ChemistryDrug DiscoverySous videMNDOReactive componentsReactivity (chemistry)BiochemistryMedicinal chemistryCycloadditionTetrahedron Letters
researchProduct

ChemInform Abstract: 1H-Naphtho(2,1-b)thiete and 2H-Naphtho(2,3-b)thiete - Synthesis and Reactivity.

2010

Abstract The title compounds 4 and 8 are obtained by flash vacuum pyrolysis of the corresponding hydroxymethylthionaphthols 3 and 7. Whereas 4 shows a smooth ring opening on heating, 8 is thermally stable but reacts photochemically. The different behavior is explained on the basis of an MNDO calculation. The valence isomers 4′ and 8′ represent thioquinonemethides, which are highly reactive components in [12π + 2π]cycloaddition processes (4 → 9, 10, 11; 8 → 12).

Valence (chemistry)Flash vacuum pyrolysisComputational chemistryChemistryMNDOReactivity (chemistry)Reactive componentsGeneral MedicineRing (chemistry)CycloadditionChemInform
researchProduct