Search results for "Lene"

showing 10 items of 4480 documents

CCDC 903571: Experimental Crystal Structure Determination

2013

Related Article: T.K.Ronson,C.Giri,N.K.Beyeh,A.Minkkinen,F.Topic,J.J.Holstein,K.Rissanen,J.R.Nitschke|2013|Chem.-Eur.J.|19|3374|doi:10.1002/chem.201203751

hexakis(mu~2~-44'-bis((Pyridin-2-ylmethylene)amino)biphenyl-22'-disulfonate)-tetra-nickel bis(hexa-aqua-nickel) tetrachloromethane tetrabromomethane clathrate hydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

CCDC 2041018: Experimental Crystal Structure Determination

2021

Related Article: Goulielmina Anyfanti, Antonio Bauzá, Lorenzo Gentiluomo, João Rodrigues, Gustavo Portalone, Antonio Frontera, Kari Rissanen, Rakesh Puttreddy|2021|Frontiers in Chemistry|9||doi:10.3389/fchem.2021.623595

hexamethylenetetramine dibromineSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

Lignin recovery from spent alkaline pulping liquors using acidification, membrane separation, and related processing steps: A Review

2019

The separation of lignin from the black liquor generated during alkaline pulping is reviewed in this article with an emphasis on chemistry. Based on published accounts, the precipitation of lignin from spent pulping liquor by addition of acids can be understood based on dissociation equilibria of weak acid groups, which affects the solubility behavior of lignin-related chemical species. Solubility issues also govern lignin separation technologies based on ultrafiltration membranes; reduction in membrane permeability is often affected by conditions leading to decreased solubility of lignin decomposition products and the presence of colloidal matter. Advances in understanding of such phenomen…

hiilidioksidiEnvironmental EngineeringrikkihappoMembrane permeabilityBioengineeringcomplex mixturesMembrane technologychemistry.chemical_compoundkalvot (elottomat objektit)Lignincolloidal stabilitySolubilitylignin isolationWaste Management and Disposaldebottlenecking of pulp millssaostusliukoisuussulfuric acidfungitechnology industry and agriculturefood and beveragesligniinimustalipeäBiorefineryPulp and paper industryacid precipitationMembranetalteenottochemistryultrafiltrationsuodatusBlack liquorKraft paperBioResources
researchProduct

Self-Assembled Molecular Rafts at Liquid|Liquid Interfaces for Four-Electron Oxygen Reduction

2011

The self-assembly of the oppositely charged water-soluble porphyrins, cobalt tetramethylpyridinium porphyrin (CoTMPyP(4+)) and cobalt tetrasulphonatophenyl porphyrin (CoTPPS(4-)), at the interface with an organic solvent to form molecular "rafts", provides an excellent catalyst to perform the interfacial four-electron reduction of oxygen by lipophilic electron donors such as tetrathiafulvalene (TTF). The catalytic activity and selectivity of the self-assembled catalyst toward the four-electron pathway was found to be as good as that of the Pacman type cofacial cobalt porphyrins. The assembly has been characterized by UV-visible spectroscopy, Surface Second Harmonic Generation, and Scanning …

inorganic chemicals2Nd-Harmonic Generationchemistry.chemical_elementPhotochemistryBiochemistryOxygenCatalysisCatalysischemistry.chemical_compoundWater-Soluble PorphyrinsColloid and Surface ChemistryCobalt Porphyrinsheterocyclic compoundsLiquid/Liquid Interface2Nd DerivativesEnergyDioxygenPolarizable Continuum ModelGeneral ChemistryPorphyrinRadical CationchemistryRadical ionSurface second harmonic generationDensity functional theoryImmiscible Electrolyte-SolutionsCobaltTetrathiafulvalene
researchProduct

Cross-Linked Imidazolium Salts as Scavengers for Palladium.

2014

Five imidazolium-based materials have been synthesised and used for the first time as palladium scavengers. Radical reactions of suitable bis-vinylimidazolium salts led to a series of insoluble materials through homo-polymerisation, immobilisation with a 3-mercaptopropyl-modified silica gel or co-polymerisation with ethylene glycol dimethylacrylate. These materials were screened as palladium scavengers with a set of palladium(0) and palladium(II) compounds in different solvents and at different starting amounts of palladium. In many cases, residual amounts of palladium were lower than 5 ppm, as requested for the manufacture of active pharmaceutical ingredients and fine chemicals. The applic…

inorganic chemicalsActive ingredientSilica gelchemistry.chemical_elementGeneral ChemistrySettore CHIM/06 - Chimica OrganicaScavenger (chemistry)chemistry.chemical_compoundchemistrySuzuki reactionIonic liquidOrganic chemistryEthylene glycolcross-coupling imidazolium salts ionic liquids palladium supported catalystsPalladiumChemPlusChem
researchProduct

The influence of cerium to urea preparation ratio of nanocrystalline ceria catalysts for the total oxidation of naphthalene

2008

The influence of cerium salt/urea ratio on the activity of nanocrystalline ceria catalysts prepared by homogeneous precipitation with urea for the complete oxidation of naphthalene has been evaluated. Ceria catalysts were prepared from five different cerium salt/urea ratios (2:1, 1:1, 1:2, 1:3 and 1:4). Catalyst characterization (by BET, XRD and TPR) only revealed subtle differences in the characteristics of these catalysts with cerium salt to urea ratio. However, Raman and scanning electron microscopy (SEM) results indicated differences in the oxygen defect concentration (FWHM of Raman band) and morphology of the catalysts with variation of the preparation ratio. Catalysts prepared with 2:…

inorganic chemicalsCerium oxideInorganic chemistrychemistry.chemical_elementGeneral ChemistryHeterogeneous catalysisCatalysisCatalysisCeriumchemistry.chemical_compoundsymbols.namesakechemistryCatalytic oxidationUreasymbolsRaman spectroscopyNaphthaleneCatalysis Today
researchProduct

Enrichment and activation of smectite-poor clay

2011

A new method of smectite clay enrichment has been developed. The method is based on dispersing clay in a phosphate solution and sequential coagulation. The product of enrichment is characterized with X-ray powder diffraction, wavelength dispersive X-ray fluorescence spectrometry, differential thermal analysis and thermogravimetry. Sorption of methylene blue and hexadecylpyridinium bromide on raw and purified clays was studied.

inorganic chemicalsChemistryInorganic chemistryFluorescence spectrometrySorptionPhosphatecomplex mixturesThermogravimetrychemistry.chemical_compoundDifferential thermal analysisClay mineralsPowder diffractionMethylene blueNuclear chemistryIOP Conference Series: Materials Science and Engineering
researchProduct

Vanadium-based Ziegler-Natta catalyst supported on MgCl2(THF)2 for ethylene polymerization

1996

A supported magnesium‐vanadium‐aluminium catalyst was prepared by depositing –with the use of a milling technique–VOCl3 on the MgCl2(THF)2 support and subsequent activation with diethylaluminium chloride. Catalytic activity of the obtained system for ethylene polymerization was evaluated as a function of Mg/V and Al/V ratios as well as catalyst ageing time and polymerization temperature. High concentrations of THF in the catalytic system and considerable excess of an organoaluminium co‐catalyst were found to have no deactivating action on vanadium active sites. The catalyst obtained is stable and its activity for ethylene polymerization is high. It yields polyethylene with higher molecular …

inorganic chemicalsDiethylaluminium chloridePolymers and PlasticsOrganic Chemistrytechnology industry and agricultureVanadiumchemistry.chemical_elementSolution polymerizationPolyethyleneCatalysischemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryCoordination polymerizationZiegler–Natta catalystMacromolecular Rapid Communications
researchProduct

Iron(iii) oxamato-catalyzed epoxidation of alkenes by dioxygen and pivalaldehyde

1997

A new iron(III)–carbonato monomeric complex of orthophenylenebis( oxamato) (opba) 1 is synthesized, and spectroscopically and structurally characterized; it is a moderately efficient non-heme catalyst for the aerobic epoxidation of alkenes with co-oxidation of pivalaldehyde. Ruiz Garcia, Rafael, Rafael.Ruiz@uv.es ; Fernandez Picot, Isabel, Isabel.Fernandez@uv.es ; Pedro Llinares, Jose Ramon, Jose.R.Pedro@uv.es

inorganic chemicalsDioxygenUNESCO::QUÍMICA::Química inorgánicaUNESCO::QUÍMICAorganic chemicalsIronMetals and AlloysIron ; Dioxygen ; Orthophenylenebis ; Catalyst ; PivalaldehydeGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]:QUÍMICA [UNESCO]CatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistryCeramics and Compositesheterocyclic compoundsCatalystOrthophenylenebisPivalaldehyde
researchProduct

Oxidative dehydrogenation of ethane: A study over the structure and robustness of Ni–W–O catalysts

2014

[EN] The robustness of one selected Ni-W-O catalyst has been studied in the oxidative dehydrogenation of ethane. This catalyst initially deactivates for the first 10 h online decreasing 15% of its catalytic activity compared to its initial stable catalytic activity. However from 10 to 60 h online the catalytic activity keeps almost stable. On the other hand, it has been shown that the Ni-W-O catalyst cannot tolerate an oxygen-free atmosphere (C-2 and He) as nickel oxide is transformed into metallic nickel. Methane and hydrogen as well as abundant coke were formed on the surface of the catalyst in these O-free conditions. However a re-calcination in air leads to the removal of coke, the cata…

inorganic chemicalsEthyleneHydrogenGeneral Chemical EngineeringCatalyst supportInorganic chemistryEnergy Engineering and Power Technologychemistry.chemical_elementCatalysisMethaneCatalysisEthylenechemistry.chemical_compoundDehydrogenationNickel tungstenOxidative dehydrogenation of ethaneOxide catalystsEthaneChemistryorganic chemicalsNickel oxideCokeFuel TechnologyNi-W-OHydrogenOxidative dehydrogenationFuel Processing Technology
researchProduct