Search results for "Thermal"

showing 10 items of 3576 documents

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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Differential calorimetric enthalpies of adsorption ofp-xylene andm-xylene on y faujasites at 25°C

1997

The differential enthalpies of adsorption ofp-xylene andm-xylene on NaY, KY and BaY zeolites were measured by isothermal calorimetry coupled with isothermal volumetry at 25‡C. Whatever the zeolite, the enthalpies of adsorption ofp-xylene andm-xylene at low filling were of the same order of magnitude. They did not show significantly the effect of the dipolar moment ofm-xylene. Their absolute values varied in the sequence

chemistry.chemical_compoundAdsorptionChromatographychemistryEnthalpyXylenePhysical chemistryIsothermal titration calorimetryCalorimetrym-Xylenep-XyleneIsothermal processJournal of Thermal Analysis
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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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Studies on the synthesis of heterocyclic compounds. Part IV. Further investigation of the pschorr reaction with some pyrazole derivatives

1980

Thermal decomposition of the diazonium sulfate derived from N-methyl-(1-phenyl-3-methylpyrazol-5-yl)-2-aminobenzamide afforded products formulated as 1-phenyl-3-methyl[2]benzopyrano[4,3-c]pyrazol-5-one (yield 10%), 1,4-dimethyl-3-phenylpyrazolo[3,4-c]isoquinolin-5-one (yield 10%), N-methyl-(1-phenyl-3-methylpyrazol-5-yl)-2-hydroxybenzamide (yield 8%) and 4′-hydroxy-2,3′-dimethyl-1′-phenylspiro[isoindoline-1,5′-[2]-pyrazolin]-3-one (yield 20%). Decomposition of the diazonium sulfate derived from N-methyl-(1,3-diphenylpyrazol-5-yl)-2-aminobenzamide gave products formulated as 7,9-dimethyldibenzo[e,g]pyrazolo[1,5-a][1,3]-diazocin-10-(9H)one (yield 8%), 4-methyl-1,3-diphenylpyrazolo[3,4-c]isoqu…

chemistry.chemical_compoundChemistryYield (chemistry)Organic ChemistryThermal decompositionOrganic chemistryPyrazoleRing (chemistry)Spectral dataMedicinal chemistryDecompositionJournal of Heterocyclic Chemistry
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ChemInform Abstract: Continuous Hydrothermal Synthesis of Nanometric BaZrO3in Supercritical Water.

2008

Abstract Nanocrystalline barium zirconate (BaZrO 3 ) was synthesized using a hydrothermal synthesis process working in supercritical conditions and in a continuous way. By this method, we succeeded in the continuous and rapid production of nanopowders. As a preliminary work three barium precursors have been investigated: barium hydroxide (Ba(OH) 2 ), barium acetate (Ba(CH 3 COO) 2 ) and barium nitrate (Ba(NO 3 ) 2 ). Two of them (Ba(CH 3 COO) 2 and Ba(NO 3 ) 2 ) led to the pure perovskite phase. Then an experimental design has been conducted in order to determine the influence of the experimental parameters on the crystallinity and the grain size of the final product.

chemistry.chemical_compoundCrystallinityBarium acetatechemistryChemical engineeringHydrothermal synthesischemistry.chemical_elementBarium nitrateBariumGeneral MedicineSupercritical fluidPerovskite (structure)Barium hydroxideChemInform
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Fast Solution Precursor Synthesis of the 2223 Phase: the Role of Lead in the Reaction Pathway

1994

ABSTRACTValuable mechanistic information, about the reaction pathway in the formation of the 2223 phase, has been obtained by the use of a solution synthesis route. The presence of lead in the starting mixture has remarkable effects on the nature and stability of the different intermediates: i) the grain size and morphology of Bi2CuO4 is severely changed, ii) calcium carbonate is partially decomposed to yield the calcium plumbate, iii) the 2201 phase results stabilized against the formation of the collapsed phase Bi17Sr16Cu7O49-δ, iv) the melting point of the intermediate 2212 is lowered by about 10 °C. All these effects, due to lead substitution, contribute to promote the formation of the …

chemistry.chemical_compoundCrystallographyCalcium carbonateMaterials sciencechemistryYield (chemistry)Phase (matter)Differential thermal analysisInorganic chemistryX-ray crystallographyMelting pointPlumbateGrain sizeMRS Proceedings
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Selective oxidative dehydrogenation of ethane on MoVTeNbO mixed metal oxide catalysts

2004

Abstract MoVTeNbO catalysts, prepared by hydrothermal synthesis, are active and highly selective in the ODH of ethane, especially those with a MoVTeNb molar ratio of 1–0.15–0.16–0.17 and heat-treated at 600–650 °C. On the best catalyst, selectivities higher than 80% at ethane conversion levels higher than 80% have been obtained operating at relatively low reaction temperatures (340–400 °C). Thus, yields of ethylene of ca. 75% have been obtained, which exceeds the best yield reported in the literature. Te 2 M 20 O 57 ( M =Mo, V, Nb) and (V,Nb)-substituted θ -Mo 5 O 14 , in addition to small amounts of the Te 0.33 M O 3.33 ( M =Mo, V, Nb) phase, can be proposed in the most selective cataly…

chemistry.chemical_compoundEthyleneChemistryYield (chemistry)X-ray crystallographyInorganic chemistryOxideHydrothermal synthesisDehydrogenationOrthorhombic crystal systemPhysical and Theoretical ChemistryCatalysisCatalysisJournal of Catalysis
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Thermal rearrangements of 1,2-dialkoxybenzenes by flash vacuum pyrolysis

1995

Flash vacuum pyrolysis of 1,2-dialkoxybenzenes 1a-c leads to the liberation of alkanes from the interacting side chains. A rearrangement of the skeleton yields the o-hydroxy carbonyl compounds 2 and 4. The generation of phenol 3 can be rationalized by a decarbonylation. The latter reaction is the sole process which can be observed for the bicyclic starting compound 9.

chemistry.chemical_compoundFlash vacuum pyrolysisBicyclic moleculeChemistryScientific methodOrganic ChemistryDecarbonylationThermalSide chainPhenolGeneral ChemistryPhysical and Theoretical ChemistryPhotochemistryLiebigs Annalen
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Soft hydrothermal synthesis of new microporous materials based on phosphate-like species

1994

ABSTRACTFactors controlling hydrothermal synthetic procedures are not well understood. A good knowledge of the solution chemistry of precursor species is the best reference for the design of rational procedures. Examples of the predictive character of simple models in order to rationalize complex syntheses are discussed in detail.

chemistry.chemical_compoundMaterials scienceChemical engineeringchemistryHydrothermal synthesisOrganic chemistrySolution chemistryMicroporous materialVanadium CompoundsPhosphateHydrothermal circulation
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