Search results for "thermal decomposition"

showing 10 items of 112 documents

Facile laser-assisted synthesis of inorganic nanoparticles covered by a carbon shell with tunable luminescence

2015

We report a one-step strategy at ambient conditions for the production of hybrid inorganic core–carbon shell nanoparticles by means of pulsed laser ablation of inorganic targets (LiNbO3, Au, and Si) in hydrocarbon liquids such as toluene and chloroform. The core of these spherical nanoparticles consists of the target material, whereas the shells are carbon structures (multilayer graphite-type carbon and amorphous carbon), which are formed due to the thermal decomposition of the organic liquid in contact with hot inorganic nanoparticles ejected from the bulk target. These carbon shells emit photoluminescence in the blue-green spectral region and the obtained luminescence, in which the lumine…

chemistry.chemical_classificationPhotoluminescenceChloroformMaterials scienceGeneral Chemical EngineeringThermal decompositionInorganic chemistryPhysics::OpticsNanoparticlechemistry.chemical_elementGeneral ChemistryCondensed Matter::Materials Sciencechemistry.chemical_compoundHydrocarbonchemistryChemical engineeringAmorphous carbonPhysics::Atomic and Molecular ClustersPhysics::Chemical PhysicsLuminescenceCarbonRSC Advances
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Crystalline CO2 -Based Aliphatic Polycarbonates with Long Alkyl Chains

2018

Carbon dioxide (CO2 ) is an easily available, renewable carbon source and can be utilized as a comonomer in the catalytic ring-opening polymerization of epoxides to generate aliphatic polycarbonates. Dodecyl glycidyl ether (DDGE) is copolymerized with CO2 and propylene oxide (PO) to obtain aliphatic poly(dodecyl glycidyl ether carbonate) and poly(propylene carbonate-co-dodecyl glycidyl ether carbonate) copolymers, respectively. The polymerization proceeds at 30 °C and high CO2 pressure utilizing the established binary catalytic system (R,R)-Co(salen)Cl/[PPN]Cl. The copolymers with varying DDGE:PO ratios are characterized via NMR, FT-IR spectroscopy, and SEC, exhibiting high molecular weight…

chemistry.chemical_classificationPolymers and PlasticsComonomerOrganic ChemistryThermal decomposition02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCatalysischemistry.chemical_compoundDifferential scanning calorimetrychemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerPropylene oxide0210 nano-technologyAlkylMacromolecular Rapid Communications
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Intramolecular coupling of acetylenic groups of bis(alkynyl)phosphanes and silanes mediated by benzynezirconocene: a route to new mono- and tricyclic…

2004

Benzo-zirconacyclohexadiene-phospha or silacyclobutene fused ring systems are easily prepared via a benzynezirconocene intermediate by means of thermolysis of Cp 2 ZrPh 2 in the presence of bis(alkynyl)phosphanes or silanes. These polyunsaturated systems are the source of a variety of new mono- or tricyclic heterocycles incorporating either one or two heteroatoms.

chemistry.chemical_classificationSilanesChemistryOrganic ChemistryHeteroatomThermal decompositionGeneral MedicinePhotochemistryRing (chemistry)BiochemistryMedicinal chemistryCoupling (electronics)chemistry.chemical_compoundC c couplingMain group elementIntramolecular forcePolymer chemistryDrug DiscoveryTricyclicTetrahedron
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Thermal decomposition study of major refuse derived fuel components

2018

Abstract Refuse Derived Fuel (RDF) composed on biomass, paper, textiles, wood, synthetic polymers and other combustible materials is an alternative energy resource to implement Waste-to-Energy strategy. The aim of this study is to investigate the thermal decomposition characteristics of materials forming RDF by thermogravimetric analysis. Thermogravimetric (TG) analysis of RDF components demonstrates major differences in processes behind the thermal decomposition processes of waste components. Biomass decomposition can be divided into two distinct stages for wood, cotton, cotton wool and other biomass samples whereas three distinct stages can be distinguished for cardboard and paper samples…

chemistry.chemical_classificationThermogravimetric analysisThermal decompositioncardboardBiomass02 engineering and technologyPolymer010501 environmental sciences021001 nanoscience & nanotechnology01 natural sciencesDecompositionCombustibilitychemistryChemical engineeringvisual_artvisual_art.visual_art_medium0210 nano-technologyRefuse-derived fuel0105 earth and related environmental sciencesEnergy Procedia
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Synthesis, optical, and thermal properties of glassy trityl group containing luminescent derivatives of 2-tert-butyl-6-methyl-4H-pyran-4-one

2012

In this work we present simple preparation of original trityl group containing glassy luminescent 6-styryl substituted derivatives of 2-(2-tert-butyl-4H-pyran-4-ylidene)malononitrile (DWK-1TB), 2-(2-tert-butyl-4H-pyran-4-ylidene)-2- ethyl-2-cyanoacetate (KWK-1TB), 2-(2-tert-butyl-4H-pyran-4-ylidene)-1H-indene-1,3(2H)-dione (ZWK-1TB) and 5-(2-tert-butyl-4H-pyran-4-ylidene)pyrimidine-2,4,6(1H,3H,5H)-trione (JWK-1TB). Their optical properties have been investigated. The absorption maxima of synthesized glasses is in region from 425 nm to 515 nm and emission maxima is from 470 nm to 625 nm in solution of dichloromethane. But absorption maxima of their solid films is from 425 nm to 500 nm and em…

chemistry.chemical_classificationchemistry.chemical_compoundMaterials sciencechemistryThermal decompositionPhysical chemistryThermal stabilityPolymerAbsorption (chemistry)Glass transitionLuminescenceDichloromethaneMalononitrileOrganic Photonics V
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1986

In order to graft methacrylonitrile onto preformed networks containing thermolabile azo groups, the monomer was used to swell the networks and then the temperature raised to the decomposition temperature for the azo groups. The unusually high grafting efficiencies yields (e) achieved are explained in terms of both the differences in the reactivities of the primary radicals formed and side reactions, which lead to additional grafting sites. As an aid to understand the dependence of monomer conversion on that of the initiator a kinetic model is discussed, which involves the consideration of the polymerization taking place both in the homogeneous phase and within the polymer pearls, which can …

chemistry.chemical_classificationchemistry.chemical_compoundMonomerchemistryPolymerizationMethacrylonitrilePolymer chemistryThermal decompositionCopolymerGeneral Materials SciencePolymerThermolabileGraftingAngewandte Makromolekulare Chemie
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Thermal and optical properties of 4H-pyran-4-ylidene fragment and bis-styryl and triphenyl groups containing derivatives

2014

Small D-π-A type organic molecules with incorporated 4H-pyan-4-ylidene (pyranylidene) fragment in their structures show potential in organic photonics - such as materials for organic light emitting diode application studies and organic solid state lasers. Additional incorporation of bulky triphenyl- groups in their structures gives them the ability to form thin amorphous solid films from volatile non-polar organic solvents. Unfortunately, there is still no clear relation between compound organic structures and their thermal and optical properties. In order to investigate the above mentioned regularities we have synthesized a series of tripheyl- group containing derivates of 2,6-bis-styryl-4…

chemistry.chemical_classificationchemistry.chemical_compoundPhotoluminescenceMaterials sciencechemistryOrganic photonicsThermal decompositionSubstituentElectron acceptorGlass transitionPhotochemistryDichloromethaneAmorphous solidSPIE Proceedings
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Synthesis and thermal decomposition studies of homo- and heteroleptic tin(iv) thiolates and dithiocarbamates: molecular precursors for tin sulfides

2002

The syntheses and X-ray structures of novel heteroleptic thiolate/dithiocarbamate derivatives (Et2NCS2)2(RS)2Sn (R = Cy, CH2CF3) have been examined and their thermal decompositions compared with those of selected tin(II) and tin(IV) dithiocarbamates. The heteroleptic species decompose to SnS by initial elimination of RSSR to afford (Et2NCS2)2Sn and subsequent loss of [Et2NC(S)]2S. In contrast, (Et2NCS2)4Sn decomposes via [(Et2NCS2)2SnS]2, whose structure has been determined, and finally to SnS2 by sequential elimination of [Et2NC(S)]2S. The two families of compounds, (R2NCS2)4Sn and (Et2NCS2)2(RS)2Sn, thus provide single-source materials for bulk SnS2 and SnS, respectively, by virtue of the…

chemistry.chemical_classificationtin thiolatesMössbauer spectroscopyChemistryInorganic chemistryThermal decompositionSolid-statechemistry.chemical_elementGeneral ChemistryCrystal structureChemical vapor depositionMedicinal chemistryDecompositionchemical vapor depositionSettore CHIM/03 - Chimica Generale E InorganicaTinDithiocarbamateX-ray crystallographyJournal of the Chemical Society, Dalton Transactions
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Evidence for the formation of 1,3- and 1,4-dehydrobenzenes in the thermal decomposition of diaryliodonium-carboxylates

1986

Abstract Abstract: Generation of m- and p-benzynes in decomposition of diaryliodonium- 3- and 4-carboxylates is demonstrated by three-phase method.

chemistry.chemical_compoundBetaineChemistryOrganic ChemistryDrug DiscoveryThermal decompositionReaction intermediatePhotochemistryBiochemistryAryneDecompositionPyrolysisTetrahedron Letters
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Bulk pre-reactional transformations preceding the thermal decomposition of calcium hydroxide into oxide

1990

The present paper is an extended abstract which should be considered as an introduction to the papers already published by us on this new topic. An extended synthesis of these papers was given in the lecture. The original information introduced here is the figure. It is a PH2O vs. T diagram which gives the pre-reactional domain between the stability domains of calcium hydroxide and calcium oxide. Chemical reactions are proposed as an interpretation of the observed pre-reactional transformations.

chemistry.chemical_compoundCalcium hydroxidechemistryInorganic chemistryThermal decompositionDiagramGeneral EngineeringOxideThermodynamicsCalcium oxideChemical reactionReactivity of Solids
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