Search results for "Catalysis"

showing 10 items of 5944 documents

Synthesis of Multisubstituted 1,4-Dihydrobenzoxazin-2-ones through a One-Pot Nucleophilic N-Alkylation/C-Alkylation of Cyclic α-Imino Esters

2017

A nucleophilic N-alkylation of 2-oxobenzoxazine-2-carboxylates with organozinc reagents with good selectivities and in moderate to good yields is described. Moreover, the synthesis of multisubstituted 1,4-dihydrobenzoxazine-2-ones bearing a tetrasubstituted carbon atom via a one-pot N-alkylation/C-alkylation reactions is reported.

Carbon atom010405 organic chemistryChemistryOrganic Chemistrychemistry.chemical_elementZincAlkylation010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesUmpolungReaccions químiquesCompostos orgànics SíntesiNucleophileOne pot reactionReagentOrganic chemistrylipids (amino acids peptides and proteins)Química orgànica
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Stanislao Cannizzaro and the Development of Chemistry in Palermo from 1862 to 1871

2009

Stanislao Cannizzaro worked at Palermo University for about ten years. There he managed to establish a modern and well-equipped chemical laboratory. His international fame attracted co-workers even from abroad: Naquet, Lieben, and Körner came to Palermo to work with him. This greatly improved the quality of teaching and of research in Palermo, which became a worldwide acknowledged center of chemical culture. In Palermo, atomic-molecular theory was extensively taught and research was carried out on chemical atomicity (valence) and spatial structures of both aliphatic and aromatic organic molecules: Körner found the relative positions of substituent groups on the benzene ring, Paternò proved …

Carbon atomChemistryOrganic ChemistryGeneral ChemistryChemical laboratorychemical educationStanislao CannizzaroCatalysisHistory of chemistryOrganic moleculeshistory of chemistryItalian Chemical SocietyQuality of teachingchemical structureCannizzaro reactionOrganic chemistrychemical valenceClassicsChemistry - A European Journal
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Studies on ultramicro- and trace analysis of organic substances

1965

Summary For the determination of about 1 μg hydrogen in nonvolatile organic compounds 10–40 μg of the substance are burnt at > 1000°C in a slow stream of oxygen. The water generated is converted to H 2 S by reaction with carbon disulfide in a flow of nitrogen at 500°C catalyzed by α-Al 2 O 3 . The hydrogen sulfide is argentimetrically titrated by a potentiometric method. The standard deviation of the method is ± 10 ng H. There are no interferences by N, S, and the halogens.

Carbon disulfideHydrogenHydrogen sulfideInorganic chemistrychemistry.chemical_elementNitrogenOxygenAnalytical ChemistryCatalysischemistry.chemical_compoundchemistryHalogenElectroanalytical methodSpectroscopyMicrochemical Journal
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Highly Efficient Electron Transfer in a Carbon Dot–Polyoxometalate Nanohybrid

2020

Using solar radiation to fuel catalytic processes is often regarded as the solution to our energy needs. However, developing effective photocatalysts that are active under visible light has proven to be difficult, often due to the toxicity, instability, and high cost of suitable catalysts. We engineered a novel photoactive nanomaterial obtained by the spontaneous electrostatic coupling of carbon nanodots with [P2W18O62]6-, a molecular catalyst belonging to the class of polyoxometalates. While the former are used as photosensitizers, the latter was chosen for its ability to catalyze reductive reactions such as dye decomposition and water splitting. We find the electron transfer within the na…

Carbon dotMaterials sciencecarbon dots photocatalysis ultrafastSettore FIS/01 - Fisica Sperimentale02 engineering and technologyRadiation010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences7. Clean energy0104 chemical sciencesCatalysisElectron transferPolyoxometalateGeneral Materials SciencePhysical and Theoretical Chemistry0210 nano-technologyVisible spectrumThe Journal of Physical Chemistry Letters
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Conversion of furfural to 2-methylfuran over CuNi catalysts supported on biobased carbon foams

2021

In this study, carbon foams prepared from the by-products of the Finnish forest industry, such as tannic acid and pine bark extracts, were examined as supports for 5/5% Cu/Ni catalysts in the hydrotreatment of furfural to 2-methylfuran (MF). Experiments were conducted in a batch reactor at 503 K and 40 bar H2. Prior to metal impregnation, the carbon foam from tannic acid was activated with steam (S1), and the carbon foam from pine bark extracts was activated with ZnCl2 (S2) and washed with acids (HNO3 or H2SO4). For comparison, a spruce-based activated carbon (AC) catalyst and two commercial AC catalysts as references were investigated. Compressive strength of the foam S2 was 30 times great…

Carbon nanofoamBatch reactorchemistry.chemical_elementkupari02 engineering and technology010402 general chemistryFurfural01 natural sciencesCatalysisCatalysischemistry.chemical_compoundkatalyytitTannic acidmedicinebiohiilicarbonGeneral Chemistrymechanical strengthfurfural021001 nanoscience & nanotechnology0104 chemical sciencesCu/Ni catalystvaahdotchemistrykatalyysisivutuotteet2-Methylfuran2-methylfurannikkeli0210 nano-technologybiobased foamsCarbonActivated carbonmedicine.drugNuclear chemistry
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Covalently Supported Ionic Liquid Phases: An Advanced Class of Recyclable Catalytic Systems

2016

In this review, the most recent advances in the synthesis and catalytic applications of covalently supported ionic liquid (IL) phases will be discussed. This class of recyclable catalytic materials is based on the covalent attachment of several types of ammonium salts, usually imidazolium, but also thiazolium, triazolium, and pyrrolidinium salts, on the surface of different supports, for example, silica, periodic mesoporous organosilica, polystyrene, magnetic-based materials, carbon nanotubes (NTs), halloysite NTs, polyhedral oligomeric silsesquioxane (POSS), and fullerenes. Moreover, poly(ionic liquid) materials, in which the IL-based structure also acts as a support, will be considered. T…

Carbon nanotubeIonic liquid010402 general chemistryHeterogeneous catalysis01 natural sciencesCatalysisCatalysislaw.inventionInorganic Chemistrychemistry.chemical_compoundHeterogeneous catalysiOrganocatalysilawOrganic chemistryPhysical and Theoretical ChemistryMetal-based catalysi010405 organic chemistryOrganic ChemistrySilsesquioxane0104 chemical sciencesMesoporous organosilicachemistryChemical engineeringOrganocatalysisIonic liquidPolystyreneCatalyst
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Application of thermally exfoliated g-C3N4 for a green selective photocatalytic oxidation of 5-hydroxymethyl-2-furfural

2016

Graphitic carbon nitride assisted partial photocatalytic oxidation of 5-hydroxymethyl-2-furfural (HMF) in aqueous medium was investigated. Different carbon nitride precursors were considered, being melamine the one yielding the most efficient photocatalyst. The obtained 30% selectivity of HMF oxidation towards 2,5-furandicarboxaldehyde (FDC) is higher than those reported up to now. A further thermal exfoliation of the g-C3N4 samples showed under artificial light irradiation both an enhanced photocatalytic activity in conversion of HMF, and selectivity (ca. 42-45 %) towards FDC. The performance of the catalysts increased when the experiments were carried out under real outdoor illumination, …

Carbon nitride selective photocatalysis 5-hydroxymethyl-2-furfural oxidationSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie
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Selective photocatalytic oxidation of 5-hydroxymethyl-2-furfural to 2,5-furandicarboxyaldehyde in aqueous suspension of g-C3N4

2017

Graphitic carbon nitride assisted partial photocatalytic oxidation of 5-hydroxymethyl-2-furfural (HMF) in aqueous medium was investigated. Different carbon nitride precursors were considered, being melamine the one yielding the most efficient photocatalyst. The obtained 30% selectivity of HMF oxidation to 2,5-furandicarboxaldehyde (FDC) is higher than those reported up to now. A further thermal exfoliation of the g-C3N4 samples showed under artificial light irradiation both an enhanced photocatalytic activity in conversion of HMF, and selectivity (ca. 42–45%) to FDC. The performance of the catalysts increased when the experiments were carried out under real outdoor illumination, reaching 50…

Carbon nitrideInorganic chemistry02 engineering and technology010402 general chemistry01 natural sciencesCatalysisCatalysisCatalysichemistry.chemical_compound5-hydroxymethyl-2-furfuralIrradiationExfoliationCarbon nitrideGeneral Environmental Science2300Process Chemistry and TechnologyGraphitic carbon nitridePartial photocatalytic oxidation021001 nanoscience & nanotechnologyCarbon nitridesExfoliation joint0104 chemical scienceschemistry25-FurandicarboxaldehydePhotocatalysisSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie5-Hydroxymethyl-2-furfural0210 nano-technologyMelamineSelectivity
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Selective photocatalytic oxidation of 5-hydroxymethyl-2-furfural in aqueous suspension of polymeric carbon nitride and its adduct with H2O2 in a sola…

2018

Abstract This work reports a study on the reactivity of polymeric carbon nitride (PCN) and PCN-H2O2 adduct samples for sunlight photocatalytic selective oxidation reactions. The characterization of these materials was reported in a previous paper where the reactivity towards the partial oxidation of 5-hydroxymethylfurfural (HMF) was studied by using two different laboratory scale photoreactors; one irradiated by UV lamps and the other one by natural sunlight. In the present study it has been confirmed the effectiveness of these C3N4 based materials for the selective partial oxidation of HMF to FDC (2,5-furandicarboxaldehyde) in aqueous medium in a pilot plant photoreactor irradiated by natu…

Carbon nitrideoxidation010402 general chemistry01 natural sciencesCatalysisAdductCatalysisBenzaldehydechemistry.chemical_compoundReaction rate constantBenzyl alcoholReactivity (chemistry)Partial oxidation4-Methoxy-benzyl alcohol010405 organic chemistryGeneral Chemistry0104 chemical scienceschemistryBenzyl alcoholSolar photocatalysis25-FurandicarboxaldehydePhotocatalysisSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie5-Hydroxymethyl-2-furfuralSelective photocatalyticNuclear chemistry
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A kinetic study of the cracking, isomerization, and disproportionation of n-heptane on a chromium-exchanged Y zeolite

1982

The kinetic rate constants for the cracking, isomerization, and disproportionation of n-heptane over a CrHNaY (32% chromium exchanged) zeolite catalyst at 400, 450, and 470 °C have been calculated. The interaction of n-heptane with a model Lewis acid such as BF3 and progress along the reaction coordinate have been studied by means of molecular orbital calculations. From the kinetic results, i.e., activation energies and frequency factors, and the theoretical calculations, it can be concluded that the controlling step in these reactions is not the formation of the carbonium ion, but the subsequent transformation of this carbonium ion. In addition, the theoretical calculations show that the a…

Carbonium ionChemistryInorganic chemistryPhysical chemistryDisproportionationLewis acids and basesPhysical and Theoretical ChemistryFluid catalytic crackingChemical reactionIsomerizationCatalysisCatalysisReaction coordinateJournal of Catalysis
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