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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 103 (1981), S. 1568-1571 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bradford : Emerald
    Anti-corrosion 50 (2003), S. 436-441 
    ISSN: 0003-5599
    Source: Emerald Fulltext Archive Database 1994-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: A variety of bisquaternary ammonium salts was prepared for the first time by reacting N,N,N',N'-tetraallyl-1,6-hexanediamine with allyl chloride, propargyl chloride, benzyl chloride, and 1-bromododecane in excellent yields (〉90 per cent). Inhibition efficiency for different concentrations of the synthesised compounds for the inhibition of corrosion of carbon steel in 1?M HCl exposed for 6?h at 60°C was determined gravimetrically. The bisquaternary salts exhibited excellent inhibition efficiencies (97-99 per cent) in the acidic solution containing 400?ppm of the inhibitor. Comparable results were obtained by the electrochemical method using Tafel plots for the inhibition efficiency of the synthesised compounds. The adsorption of these compounds on carbon steel surface was found to obey Temkin's adsorption isotherm. The work marked the beginning of constituting an important class of new inhibitors containing multiple adsorption centres of positive nitrogens as well as p-donor moieties.
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  • 3
    Electronic Resource
    Electronic Resource
    Bradford : Emerald
    Anti-corrosion 50 (2003), S. 201-207 
    ISSN: 0003-5599
    Source: Emerald Fulltext Archive Database 1994-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Several cyclic hydroxylamines containing hydrophobic substituents were prepared. All these hydroxylamines were tested for corrosion inhibition of carbon steel in 1M HCl at 60°C by gravimetric and electrochemical methods. All compounds showed excellent corrosion inhibition efficiency (IE per cent) in acidic solutions containing 400?ppm of the inhibitors; Inhibitor Efficiencies in the range 66-98 per cent were measured by the gravimetric method. Comparable results were obtained by the electrochemical method using Tafel plots for the IE of some of the selected synthesised compounds.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 24 (1994), S. 759-762 
    ISSN: 1572-8854
    Keywords: Sulfonamide ; methanesulfonanilide ; crystal structure ; molecular structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The title compound, crystallizes in the triclinic space group $$P\bar 1$$ witha=8.232(4),b=9.159(2),c=10.230(3)Å. α=74.07(3)°, β=72.50(4)°, γ=63.65(3)° andZ=2. The structure was solved by direct methods and refined by full matrix least squares methods toR=0.054 for 1817 observed reflections. The plane containing the nitrogen and sulfur atoms is perpendicular to the aromatic plane. One of the S−O bonds in each methanesulfonyl group is in nearly eclipsed conformation with the N−C bond.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 23 (1993), S. 143-148 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The title compound, a 1,3-dipolar cycloaddition product, crystallizes in the monoclinic space groupP21/c, witha=8.199(3),b=16.908(1),c=10.248(2)Å,β=93.58(2)° andZ=4. The structure was solved by direct methods and refined by full matrix least squares methods toR=0.038 for 1687 observed reflections. The stereochemistry of this compound was found to have the “ee” conformation in the solid state as well as in solution. The piperidine ring in the molecule is in the chair form and the isoxazolidine ring adopts an envelope conformation.
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  • 6
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The title compound crystallizes in the monoclinic space group P21/a, witha+12.906(9).b+11.604(2).c+14.631(9) Å, β=108.70(3)° andZ+4. The structure was solved by direct methods from diffractometer data and refined to a finalR value of 0.057 for 2020 independent reflections. The structure analysis confirms the cis disposition of the bulky substituents and indicates a puckered four-membered ring with a dihedral angle of 18.5° as expected for a non-centrosymmetrically substituted cyclobutanone.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 6 (1993), S. 326-332 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The 13C NMR spectra of most of the substituted perhydro-1,2-oxazolo[3,2-c] [1,4]oxazines (3) at low temperature showed the presence of two isomers of unequal populations. The major isomer is shown to be the cis isomer {except in 2-hydroxymethyl-2-methylperhydro-1,2-oxazolo[3,2-c] [1,4] oxazine (3e)}, which is in equilibrium with the minor isomer (trans conformer) by a relatively slow nitrogen inversion. Intramolecular hydrogen bonding in oxazines, having 2-hydroxymethyl substituents, is shown to be an important factor in determining the population ratio of the two isomers. The barrier to nitrogen inversion was determined by detailed band-shape analysis of proton and carbon NMR spectra and were in the range 66·3-72·9 kJ mol-1. The chair inversion had been slowed down, in one case, trans-dimethylperhydro-1,2-oxazol[3,2-c] [1,4]oxazine-2,3-dicarboxylate (3j), to show the presence of the two forms of the cis isomers. The barrier to chair inversion is 41·5 kJ mol-1 as determined by proton NMR band-shape analysis of 3j.
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 57 (1995), S. 343-352 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In this study, a novel series of water-soluble hydrophobically modified poly(vinyl alcohol) (PVA) is prepared by chemical modification of PVA, with the objective of investigating the polymer's rheological behavior for enhanced oil recovery applications. The solution viscosity of the polymer obtained is studied with respect to the polymer concentration, temperature, salinity, polymer modification, aging, shear rate, and polymer molecular weight. The solution viscosity of the PVA is greatly enhanced by the modification. The modified PVA exhibits a relatively high salt tolerance, typical of nonionic polymers, in the range of 0-7.0 wt % NaCl concentrations, and the viscosity of the polymer solution is relatively invariant with NaCl above 3.0 wt % NaCl concentration. Below 3 wt %, the viscosity shows a maximum then a minimum, an unusual behavior. Generally, the polymer exhibits an almost constant viscosity at high shear rates and a typical shear thinning behavior at low shear rates. In addition, increasing polymer concentration and molecular weight leads to an increase in the polymer solution viscosity. Moreover, the polymer exhibits smaller solution viscosity at a high temperatre, and a slight decrease in viscosity is also exhibited by the modified polymer with aging. Comparison of the viscosities of 18 polymer modifications indicates that the larger the numbers of hydrophobic groups (side chains) in the polymer structure, the smaller the viscosity. Moreover, the longer the hydrophobic groups (side chains) in the polymer structure, the greater the viscosity, if their number is small. © 1995 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 193 (1992), S. 2175-2187 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The copolymerization of acrylic monomers (M) [acrolein (AL), methyl acrylate (MA), acrylamide (AM) and acrylonitrile (AN)] with liquid sulfur dioxide (S) at low temperature and high dilution in the presence of tert-butyl hydroperoxide gives high SO2 incorporation into the resulting copolymers. Analysis of the composition of these polysulfones, by elemental analyses and 13C NMR, shows that they consist mostly of the MMM, SMM, MMS and MSM triad monomer sequences. Thermal (TG) analyses of selected samples demonstrate that their thermal stability, up to 30% weight loss, increases for different acrylic comonomers as follows: AL 〈 AM 〈 MA 〈 AN. Preliminary flammability tests revealed that flame retardancy increases with increasing SO2 content in the copolymer.
    Additional Material: 2 Ill.
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  • 10
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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