Search results for "titanium"

showing 10 items of 878 documents

Synthesis and catalytic studies of Ti-anchored disilanol isobutyl-POSS/alkylaluminum system

2012

Abstract Titanium (IV) precursors anchored to alkyl substituted polyhedral oligomeric silsesquioxane (POSS) disilanol were prepared and characterized. These catalysts formulated as [Ti(O^O)2] and [M(O^O)XCl] are found to be active in polymerization of ethylene at high temperatures in combination with ethylaluminum sesquichloride (Et3Al2Cl3) as co-catalyst. The polyethylene product so obtained is linear, crystalline and displays narrow dispersities. The unique low molecular weight PE formed in this reaction exhibit properties that have potential industrial applications. The effect of various reaction parameters on catalyst performance is described.

chemistry.chemical_classificationEthyleneChemistryProcess Chemistry and Technologychemistry.chemical_elementPolyethyleneCatalysisSilsesquioxaneCatalysischemistry.chemical_compoundPolymerizationEthylene polymerizationPolymer chemistryPhysical and Theoretical ChemistryAlkylTitaniumJournal of Molecular Catalysis A: Chemical
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Photocatalytic degradation of 4-nitrophenol in aqueous suspension by using polycrystalline TiO2 impregnated with functionalised Cu(II)-porphyrin or C…

2003

The photocatalytic activity of polycrystalline TiO2 samples impregnated with functionalized Cu(II)- or metal-free porphyrins has been investigated. A probe reaction, i.e., 4-nitrophenol (4-NP) photodegradation in aqueous suspension, has been used. The results indicated that the presence of the sensitizers is beneficial for the photoactivity and suggest an important role of Cu(II). A comparison with similar samples impregnated with modified Cu(II)- and metal-free phthalocyanines showed that the presence of porphyrin is more beneficial both for the decomposition rate of 4-nitrophenol and for the disappearance of nonpurgeable organic carbon (NPOC). Experiments were carried out by using cutoff …

chemistry.chemical_classificationInorganic chemistryNitro compound4-NitrophenolPorphyrinCatalysisCatalysisTitanium oxidechemistry.chemical_compoundchemistryPhthalocyaninePhotocatalysisPhysical and Theoretical ChemistryPhotodegradation
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Tailoring the ligand structure to the reagent in the mandelamide-Ti(IV) catalyzed enantioselective addition of dimethyl- and diethylzinc to aldehydes

2007

Amides derived from (S)-(+)-mandelic acid in the presence of titanium isopropoxide catalyze the enantioselective addition of dimethyl- and diethylzinc to aldehydes with good yields and ee up to 90%. Because of the modular character of the mandelamides, the structure of the ligand can be tailored to obtain the best results with each reagent. Thus, best results with dimethylzinc are obtained with N-benzyl mandelamide while N-(pyridin-2-yl) mandelamide is the best ligand for the addition of diethylzinc.

chemistry.chemical_classificationLigandProcess Chemistry and TechnologyDimethylzincEnantioselective synthesisDiethylzincAlkylationAldehydeCombinatorial chemistryCatalysischemistry.chemical_compoundchemistryReagentOrganic chemistryPhysical and Theoretical ChemistryTitanium isopropoxideJournal of Molecular Catalysis A: Chemical
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Linked Benzylamido-Cyclopentadienyl Ligands: Synthesis and Characterization of Alkyl Titanium Complexes

1997

Titanium complexes of the general type Ti(η5:η1-C5H4Si-Me2NCH2C6H3X2-2,5)Cl2 (XH, F), containing a linked benzylamido-cyclopentadienyl ligand, were prepared by reaction of Ti(η5-C5H4SiMe2Cl)Cl3 with lithium amide Li(NHCH2C6H3X2-2,5). A single-crystal X-ray structural analysis of Ti(η5: η1-C5H4SiME2NCH2C6H3F2-2,5)Cl2 revealed a conformation in the solid state in which the aryl ring is turned away from the metal center. Ti(η5:η1-C5H4SiMe2NCH2C6H5)Cl2 can be alkylated with a variety of reagents to form extremely sensitive complexes of the type Ti(η5-C5H4SiMe,2NCH2C6H5)R2 (RMe, CH2 C6H5, CH2SiME3, CH2CMe2C6H5). Reaction of Li2[C5Me4SiMe2NCH2C6H5] with TiCl3(THF)3 gave Ti(η5: η1-C5Me4SiMe2NCH2C6…

chemistry.chemical_classificationLithium amideLigandStereochemistryArylchemistry.chemical_elementAlkylationInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryCyclopentadienyl complexLewis acids and basesAlkylTitaniumChemische Berichte
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Biologizing titanium alloy implant material with morphogenetically active polyphosphate

2015

As a further step towards a new generation of bone implant materials, we developed a procedure for biological functionalization of titanium alloy surfaces with inorganic calcium polyphosphate (Ca-polyP). This polymer has been demonstrated to exhibit morphogenetic activity. The coating of titanium oxidized Ti-6Al-4V scaffolds with biologically active amorphous Ca-polyP microparticles is formed by Ca2+ ion bridges to the silane coupling agent APTMS. This surface is durable and stable as an almost homogeneous Ca-polyP layer onto the metal. The homogenously coated Ca-polyP titanium scaffold was found to be biologically active and supported the growth and functional activity of bone cell-related…

chemistry.chemical_classificationMaterials scienceGeneral Chemical EngineeringPolyphosphateMetallurgytechnology industry and agricultureTitanium alloychemistry.chemical_elementGeneral ChemistryPolymerengineering.materialequipment and suppliesMetalchemistry.chemical_compoundchemistryCoatingChemical engineeringvisual_artvisual_art.visual_art_mediumengineeringSurface modificationLayer (electronics)TitaniumRSC Advances
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Superhydrophobic TiO2/Fluorinated Polysiloxane Hybrid Coatings with Controlled Morphology for Solar Photocatalysis

2021

Abstract Technological applications of polysiloxane coatings have been influenced by their intrinsic low surface energy, which increases their water repellence. Accurate control of composition and interfacial properties through the introduction of perfluorinated moieties further lowers the polysiloxane surface energy, while mixing with metal oxide nanoparticles enhances roughness, resulting in a great potential in the development of superhydrophobic materials for photocatalysis. Herein, a series of hydrophobic and superhydrophobic hybrid coatings were prepared by dehydrocoupling and hydrosilylation reactions of polymethylhydrosiloxane with 1H,1H,2H,2H‐perfluorooctyltriethoxysilane and 1,3-d…

chemistry.chemical_classificationMaterials sciencePolymethylhydrosiloxaneHydrosilylationtitanium dioxidePMHSPolymerSurface energyContact anglechemistry.chemical_compoundColloid and Surface Chemistryhybrid coatingschemistryChemical engineeringPhotocatalysisfluorinated polysiloxanesWettingFourier transform infrared spectroscopyphotocatalysissuperhydrophobicitySettore CHIM/02 - Chimica Fisica
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Production of titanium ion beams in an ECR ion source

2002

Abstract Intensive highly charged Ti ion beams were successfully produced in the 14 GHz ECR ion source at the Accelerator Laboratory, University of Jyvaskyla (JYFL). The Ti beams were produced using the MIVOC technique, i.e. by allowing the vapor of an organic compound containing titanium to diffuse into the ion source at room temperature. After optimizing the source parameters the intensity of the 48 Ti 11+ ion beam reached a value of 45 μA.

chemistry.chemical_classificationNuclear and High Energy PhysicsMaterials scienceIon beamAnalytical chemistrychemistry.chemical_elementTitanium ionOrganic compoundIon sourceIonIon beam depositionchemistryPhysics::Plasma PhysicsPhysics::Accelerator PhysicsAtomic physicsInstrumentationTitaniumNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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Synthesis of all-syn Functionalized Triphenylene Ketals

2011

The stereoselective synthesis of triphenylene ketals offers access to unique scaffolds. For a good performance in supramolecular applications an all-syn orientation of the functional groups is essential. The oxidative trimerization of catechol ketals by molybdenum pentachloride or mixtures with titanium tetrachloride leads to a template-directed formation. Several heterocyclic moieties are suitable for this transformation. A template-directed isomerization of anti,anti,syn isomers to the desired C 3 -symmetric derivative was demonstrated in two cases.

chemistry.chemical_classificationOrganic ChemistryAcetalSupramolecular chemistryTriphenyleneChemical synthesischemistry.chemical_compoundchemistryHeterocyclic compoundFunctional groupTitanium tetrachlorideOrganic chemistryPhysical and Theoretical ChemistryIsomerizationEuropean Journal of Organic Chemistry
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Photoelectrocatalytic selective oxidation of 4-methoxybenzyl alcohol in water by TiO2 supported on titanium anodes

2013

The photoelectrocatalytic partial oxidation of 4-methoxybenzyl alcohol in aqueous solution irradiated by near-UV light was carried out in a three-electrode batch reactor. TiO2 films were either deposited by dip-coating of a TiO2 sol onto a Ti foil and subsequent calcination or generated on Ti plates by thermal oxidation in air at 400-700 degrees C. The effects of the anode preparation method and bias potential values on conversion and selectivity to the corresponding aldehyde were investigated. The photoelectrocatalytic results were compared with the photocatalytic and electrocatalytic ones. The results indicated that no reaction occurred during the electrocatalytic experiments, whereas the…

chemistry.chemical_classificationPhotoelectrocatalysis Titanium TiO2/Ti 4-Methoxybenzaldehyde Aromatic alcohols Green synthesisProcess Chemistry and TechnologyInorganic chemistryAlcoholAldehydeCatalysislaw.inventionchemistry.chemical_compoundchemistrylawBenzyl alcoholSaturated calomel electrodePhotocatalysisCalcinationReactivity (chemistry)Partial oxidationGeneral Environmental Science
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Photocatalytic Selective Oxidation of 4-Methoxybenzyl Alcohol to Aldehyde in Aqueous Suspension of Home-Prepared Titanium Dioxide Catalyst

2007

WOS: 000246040000026

chemistry.chemical_classificationTitanium DioxideAqueous solutionInorganic chemistryAlcoholGeneral ChemistrySelective OxidationAldehydeCatalysischemistry.chemical_compoundchemistryAlcohol oxidationTitanium dioxideTitanium tetrachloridePhotocatalysisPhotocatalysisP-Anisaldehyde ProductionAdvanced Synthesis & Catalysis
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