Search results for "alkali"

showing 10 items of 566 documents

Über katalytische einflüsse bei der polykondensation des p-kresoldialkohols

1952

Wird natriumfreier p-Kresoldialkohol in Silber- oder Platingeraten bei 130°C kondensiert, so ist durch den Geruch kein Formaldehyd wahrnehmbar. p-Kresoldialkohol enthalt oft von seiner Darstellung uber das Natriumsalz her geringe Mengen an Natrium, dessen Anteil im Bereich von 0,0 bis 5,00/00 liegt (0,000 bis 0,037 Mol Natrium je Mol Phenolalkohol). Die bei der Hartung des p-Kresoldialkohols in Platin- oder Silbergeraten beobachteten Gewichtsverluste und die Formaldehydabspaltung sind umso hoher, je groser der Natriumgehalt ist. Natriumfreier p-Kresoldialkohol in Gefasen aus Jenaer Gerateglas 20 und aus gewohnlichem Glas gehartet zeigt in Ubereinstimmung mit der Abgabefahigkeit an Alkali de…

chemistry.chemical_compoundChemistrySodiumPolymer chemistryFormaldehydechemistry.chemical_elementPhenolAlkali metalSodium saltDie Makromolekulare Chemie
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ChemInform Abstract: Cobalt Clusters with Cubane-Type Topologies Based on Trivacant Polyoxometalate Ligands.

2016

Four novel cobalt-substituted polyoxometalates having cobalt cores exhibiting cubane or dicubane topologies have been synthesized and characterized by IR, elemental analysis, electrochemistry, UV–vis spectroscopy, X-ray single-crystal analysis, and magnetic studies. The tetracobalt(II)-substituted polyoxometalate [Co4(OH)3(H2O)6(PW9O34)]4– (1) consists of a trilacunary [B-α-PW9O34]9– unit which accommodates a cubane-like {CoII4O4} core. In the heptacobalt(II,III)-containing polyoxometalates [Co7(OH)6(H2O)6(PW9O34)2]9– (2), [Co7(OH)6(H2O)4(PW9O34)2]n9n– (3), and [Co7(OH)6(H2O)6(P2W15O56)2]15– (4), dicubane-like {CoII6CoIIIO8} cores are encapsulated between two heptadentate [B-α-PW9O34]9– (in…

chemistry.chemical_compoundCrystallographychemistryCubanePolyoxometalatechemistry.chemical_elementGeneral MedicineType (model theory)ElectrochemistrySpectroscopyAlkali metalCobaltExchange modelChemInform
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Bestimmung des vernetzungsgrades schwach vernetzter, noch löslicher copolymerer aus styrol und bisacrylsäurephenylestern durch hydrolytischen abbau

1970

Aus Styrol und Bisacrylsaurephenylester durch radikalische, vernetzende Polymerisation erhaltene und in Toluol sowie Dioxan noch losliche Copolymere wurden durch alkalische Hydrolyse gezielt in die linear strukturierten Bestandteile zerlegt. Diese enthielten neben sehr vielen Styrolbausteinen wenige aus dem Vernetzer stammende Acrylsaurebausteine. UV-Spektren zeigten, das die Vernetzerreste durch den hydrolytischen Abbau vollstandig abgespalten waren. Von den linearen Baustucken wurden viskosimetrisch, osmometrisch und z. T. colorimetrisch die Molekulargewichte bestimmt. Die Hydrolyseprodukte zeigten eine unerwartet bei 320 mμ auftretende Extinktion, deren Ursache nicht restlos aufgeklart w…

chemistry.chemical_compoundHydrolysischemistryMolecular massPolymerizationCovalent bondPolymer chemistryCopolymerAlkaline hydrolysis (body disposal)StyreneAcrylic acidDie Makromolekulare Chemie
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Die Kationische ɛ-Caprolactam-Polymerisation. V. Die quantitative Bestimmung der N-Acyllactam-Gruppen bei der Initiierung mit wasserfreien Säuren und…

1971

Als Beitrag zur Aufklarung des Mechanismus der kationischen Caprolactam-Polymerisation mit wasserfreien Sauren (z. B. HCl) als Initiatoren wurde der Gehalt der C-terminal entstehenden N-Acyllactam-Endgruppen und anderer funktioneller Gruppen der gebildeten Oligo- und Polyamide quantitative bestimmt. Dies erfolgte auf IR-spektroskopischem Wege und durch potentiometrische Titration der nach alkalischer Hydrolyse gebildeten Carboxylgruppen. Fur die Polymerisation wurde ein verbessertes Verfahren ausgearbeitet, das vollstandigen Sauerstoff- und Feuchtigkeitsausschlus ermoglicht und damit besser reproduzierbare Ergebnisse liefert. Die Abhangigkeit der Konzentration verschiedener funktioneller Gr…

chemistry.chemical_compoundPolymerizationChemistryHydrochloridePotentiometric titrationPolymer chemistryCationic polymerizationCaprolactamLactamTitrationAlkaline hydrolysis (body disposal)Die Makromolekulare Chemie
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Mechanism of stereospecific polymerization of styrene with alkali metal alkyls

2007

chemistry.chemical_compoundStereospecificitychemistryPolymerizationPhotochemistryAlkali metalMechanism (sociology)StyreneJournal of Polymer Science Part C: Polymer Symposia
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The initial stages of the heterogeneous degradation of alkali cellulose by oxygen in relation to the morphology of native cotton cellulose

2007

Treatment of cotton cellulose with sodium hydroxide solutions of varying concentration over extended periods in the absence of oxygen markedly decreases the intrinsic viscosity of both the cellulose in cuoxam and its cellulose trinitrate derivative (CTN) in acetone. Light-scattering measurements show that the molecular weight does not change while the radius of gyration decreases and the second virial coefficient increases. The narrow molecular weight distribution of the native cotton is still maintained. Mild oxidation first causes the intrinsic viscosity to increase. At more prolonged oxidation times the viscosity decreases. These results are interpreted by an intramolecular cross-linking…

chemistry.chemical_compoundViscosityChemical engineeringchemistryVirial coefficientSodium hydroxideIntrinsic viscosityPolymer chemistryGeneral EngineeringRadius of gyrationMolar mass distributionCelluloseAlkali metalJournal of Polymer Science: Polymer Symposia
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Revision of Na 2 A1Σ+u state molecular constants by polarization labeling spectroscopy

1997

ABSTRACT. This paper contains the analysis of the A1 of Na2 based on the data obtained from thepolarization labeling spectroscopy experiment on the A' —X' transition. A set of Dunham coefficients is derived, which describes the A state in the wide range of v and J 126) quantum numbers and reproduces the positions of unperturbed rotational lines in the A-X band system towithinO.1 cm'.1. INTRODUCTION.We report' new analysis of the A' state based on the data obtained from polarization labelingspectroscopy (PLS) experiment"2, based on V-type optical—optical double resonance scheme, on the 1 : ' ; band system of sodium dimer. The diatomic alkali molecules, with their simple electronic configurat…

chemistry.chemical_compoundchemistryDimerAnalytical chemistryMoleculeElectron configurationAtomic physicsQuantum numberSpectroscopyPolarization (waves)Alkali metalDiatomic moleculeSPIE Proceedings
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PHOSPHORORGANISCHE VERBINDUNGEN 105.1Synthese chiraler und achiraler ditertiärer 1-Phosphino-2-Aminoethan-Derivate ([dbnd]P [sbnd]CH2[sbnd]CHR[sbnd]N…

1983

Abstract Primary amines with an optical active ligand add to vinyl- and propenylphosphonium salts according the reaction schemes (5) and (6), forming compounds of the type E and F. F contains a new asymmetric center in the bridge giving rise to the formation of a mixture of diastereomers, which can be resolved. Phosphonium salts of type E and F with a benzyl group on the phosphonium center are cleaved reductively by alkali amalgams (Li/Hg; Na/Hg; K/Hg) forming tertiary phosphines with an aminogroup in the β-position. The reductive cleavage with alkali amalgams is superior to the cathodic cleavage. Application: The synthesis of Ni(O)- and Pd(O)-complexes of type J fails. Bis-phosphine comple…

chemistry.chemical_compoundchemistryLigandHomogeneousStereochemistryReductive cleavageBenzyl groupDiastereomerPhosphoniumCleavage (embryo)Alkali metalMedicinal chemistryPhosphorus and Sulfur and the Related Elements
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DELAYED ELECTRON EMISSION OF NEGATIVELY CHARGED TUNGSTEN CLUSTERS

1996

The delayed electron emission of negatively charged tungsten clusters has been investigated on a time scale from 1 to 500 ms. After being stored in a Penning trap clusters ions [Formula: see text] were heated via multiphoton absorption (hν=1.81 eV). In contrast to alkali and coinage metals no photofragmentation could be detected. Instead, for all cluster sizes studied so far only a decrease in the initial ion intensity as a function of time after excitation was observed. This decrease is not caused by ion loss from the trap, but has to be attributed to neutralization via delayed electron emission. The presented results strongly suggest that this process can be viewed as “thermionic emissio…

chemistry.chemical_elementCoinage metalsThermionic emissionSurfaces and InterfacesElectronTungstenCondensed Matter PhysicsAlkali metalPenning trapSurfaces Coatings and FilmsIonchemistryMaterials ChemistryAbsorption (chemistry)Atomic physicsSurface Review and Letters
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Multiple origins of methane in fluids circulating in the Othrys ophiolite, central Greece

2018

The complex geology of Greece includes two important parallel running ophiolitic belts. The Othrys Massif in central Greece belongs to westernmost of them. In and around this wide ophiolite outcrop, some cold hyperalkaline and some hypothermal (T < 40°C) alkaline springs are present. Thirty water samples were collected at 17 different sites and both bubbling and dissolved gases were analysed for their chemical (He, Ne, H2, O2, N2, CH4, C2H6, CO2 and H2S) and isotope (He, δ13C-CO2, δ 13C-CH4, δ 2H-CH4) composition. All samples except one have H2S contents below detection limit (10 μmol/mol), whilst H2 (from <2 to 2500 μmol/mol), CO2 (up to 26,000 but generally below 1000 μmol/mol) and …

continental serpentinization hyperalkaline springs bubbling and dissolved gasesSettore GEO/08 - Geochimica E Vulcanologia
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