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  • Polymer and Materials Science  (6)
  • 21.30.+ y  (1)
  • 1985-1989  (4)
  • 1980-1984  (1)
  • 1970-1974  (2)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 595-599 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymers of tributyltin methacrylate (M1) with cyclohexyl methacrylate, ethoxyethyl methacrylate, ethyl methacrylate, 2-hydroxyethyl methacrylate, and 2-hydroxypropyl methacrylate were synthesized in solution at 55°C utilizing azobisisobutyronitrile initiator. Copolymer compositions were determined by tin analysis; monomer reactivity ratios were calculated by Kelen-Tüdös method. Since the reactivity ratios indicate the distribution of different monomer units in the polymer chain, the measured values are compared and discussed. Preliminary results of the biotoxicity studies on some of the copolymers are also reported.
    Additional Material: 2 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 4421-4438 
    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: The second stage of batch poly(ethylene terephthalate) (PET) reactor with bis(2-hydroxyethyl) terephthalate (BHET) as the feed has been simulated. In this stage, the overall polymerization is not diffusion limited and is known to be a complex reaction. In this work it has been assumed to consist of polycondensation, reaction with monofunctional compounds (cetyl alcohol), redistribution, and cyclization reactions. The forward and reverse steps of each of these have been modelled in terms of the rate constants involving functional groups and the reacted bonds. The equations for the calculation of the molecular weight distribution (MWD) in batch reactors have been written and solved numerically. The MWD reported in this work is assumed to include the monofunctional products only, and, for the case where ethylene glycol is not removed from the reaction mass, it was found to be unaffected by the choice of the redistribution rate constant (kr). Since the removal of ethylene glycol is not mass transfer controlled, its concentration in the reaction mass is assumed be given by the vapor-liquid equilibrium existing at the pressure applied on the reactor. In this work, the level of ethylene glycol concentration, yg (≡[G]/[P1]0), has been taken as a parameter, and, on application of vacuum, the MWD results were found to vary with kr with the sensitivity increasing with yg. It was then shown that the importance of the redistribution reaction is enhanced when the cyclization reaction also occurs. The effect of vacuum on the performance of the reactor has been studied by varying yg. For yg less than 0.01, the change in the MWD of the polymer becomes very small. The effects of polymerization temperature and initial concentration of monofunctional compounds on MWD were found to be small.
    Additional Material: 10 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 1095-1112 
    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: Hydroxyl terminated natural rubber (HTNR) was prepared by the depolymerization of masticated natural rubber in the presence of H2O2 in toluene. Probable mechanisms leading to the formation of side reaction products are proposed based on the analytical data. A comparative study of some formulation variables was made for their effect in improving the flow characteristics and mechanical properties of an aluminized polyurethane (PU) propellant system based on HTNR. This PU system has also been compared for its theoretical performance characteristics with some other state-of-the-art systems.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 326 (1987), S. 191-193 
    ISSN: 1434-601X
    Keywords: 25.40.Ve ; 13.75.Cs ; 21.30.+ y
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The elementary reaction pp→nΔ + +, through which the6Li(p, Δ + +)6He reaction proceeds, is considered as the flip of spins and isospins of two quarks, one in each of the two quark bags of the interacting nucleons. Using the experimental data on the6Li(p, Δ + +)6He reaction at 1.04 GeV and the distorted wave Born approximation (DWBA) for the reaction mechanism, the strength of the spin-isospin quark-quark interaction is determined. It is found to be 70 MeV fm3.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 32 (1986), S. 4541-4552 
    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: Drying rate studies were carried out with polyamic acid solution synthesized in the laboratory in dimethyl acetamide solvent, with a view to determine the process design parameters of a continous polyimide film casting machine. Studies reveal that drying under natural convection condition takes an unduly long time, whereas drying under induced draft/recirculation with partial recycle condition takes only ⅓ the time that of natural convection drying. Another important observation made was that under natural convection drying condition the initial adjustment period was too long and that the drying process was evenly spread over the initial adjustment, constant, and falling rates of the drying periods, whereas under induced draft condition drying mostly took place during the falling rate of drying period. The drying rate data obtained was used for generating the necessary process design, and operating parameters for a continuous polyimide film casting machine.
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 15 (1971), S. 147-156 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Der Einfluß von γ-Strahlen auf Hexachlorendomethylenhexahydrophthalsäure (HCPS) enthaltende ungesättigte Polyester wurde untersucht. Dazu wurden vier Polyester mit verschiedenem Molverhältnis an Chlorendic-Säure zu Isophthalsäure mit einer Co60-Quelle bestrahlt. Durch die Bestrahlung erniedrigt sich der Chlorgehalt stark mit zunehmendem Gehalt an Isophthalsäure. Mit steigendem Gehalt an HCPS nimmt die durch die Bestrahlung hervorgerufene Änderung der Säurezahl ab. Die Grenzviskosität steigt bei Polyestern, die viel Isophthalat-Gruppen enthalten, und fält bei solchen mit hohem Gehalt an HCPS. Der Einfluß der γ-Be-strachlung auf das Verhätnis von cis- und trans-Form in diesen Polyestern wurde an Infrarotspektren untersucht. Es zeigt sich, daß mit zunehmendem Gehalt an HCPS die durch die Bestrahlung verursachte trans-cis-Umwandlung stark ansteigt.
    Notes: The effect of gamma ray irradiation on chlorendic acid based unsaturated polyesters was studied. Four different types of unsaturated polyesters, made by varying the molar ratios of chlorendic acid to isophthalie acid were irradiated with a Co60 qource. After irradiation, the chlorine content decreases rapidly as the isophthalate content in the polyester chain increases. As the chlorendle acid content increases, the change in acid value after irradiation decreases. The increase in intrinsic viscosity is quite marked in high isophthalate containing polyesters after gamma ray irradiation and there is a noticeable decrease in intrinsic viscosity after gamma irradiation of high chlorendic acid containing polyesters. The effect of gamma irradiation on the percentage of cis and trans forms of these polyesters was studied with the help of infrared spectra. It appears that as the chlorendic acid content increases, on gamma irradiation conversion from trans unsaturation to cis unsaturation increases rapidly.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 139 (1970), S. 103-113 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Maleinsäure/Fumarsäure-Isomerisierung in ungesättigten Polyestern konnte mittels IR-Spektren untersucht werden, ohne daß Modellverbindungen notwendig waren. Hierzu diente die Lösung folgender Gleichung für zwei verschiedene Polyester oder für einen Polyester bei zwei Konzentrationen, um die molaren dekadischen Extinktionskoeffizienten für den Maleinsäurebaustein bei 675 cm-1 und für den Fumarsäurebaustein bei 980 cm-1 zu ermitteln Die Prozentgehalte an Malein- und Fumarsäurebausteinen sind durch folgende Gleichungen gegeben: Wegen sterischer Hinderung erscheint die CH-Schwingung (out of plane) für Maleinsaure bei der etwas niedrigeren Frequenz 675 cm-1. Steigendes Verhältnis Maleinsäure zu gesättigter Säure im Polyester vermehrte die Inversion von Maleinsäure zu Fumarsäure wegen der vergrößerten Knäuelung und Erhöhung der Knäueldichte. Das gleiche zeigte sich bei Polyestern aus Phthälsaureanhydrid wegen der o-ständigen Carboxylgruppe und im Vergleich mit Adipinsäure und Isophthalsäure, denn die Isomerisierung von Maleinzu Fumarsäure war in Polyestern aus Phthalsäureanhydrid größer als bei jenen aus Isophthalsäure und Adipinsäure. Enthielten die Polyester auch Bisphenol-A-bausteine, so war die Isomerisierung gering, weil die Phenylbausteine eine geringere Knäuelung verursachen. Dagegen stieg der Isomerisierungsgrad bei Polyestern mit 2.2-Di-(4-hydroxy-3.5-dibromphenyl)-propan und 2.2-Di-(4-hydroxy-3.5-dichlorphenyl)-propan wegen der gro̊eren sterischen Hinderung. Jedoch ist es auch möglich, daß geringe, wahrend der Polykondensation frei gewordene Halogenmengen die Isomerisierung katalysierten. Das gleiche wurde mit Polyestern, die auch Chlorendicsäure (1.4.5.6.7.7-Hexachlor-5-norbornen-2.3-dicarbonsäure) enthielten, beobachtet ; der Grad der Isomerisierung stieg mit wachsendem Säureanteil. Die stärkere Katalyse wird auf die kleinere Bindungsenergie nicht aromatisch gebundenen Halogens zurückgeführt.
    Notes: For study of maleate/fumarate isomerisation in unsaturated polyesters infrared technique was used without using model compounds. This was done by solving the following equation for two different polyesters or one polyester with two concentrations for the molar extinction coefficients at 675 cm-1 for maleate and 980 cm-1 for fumarate. Percentages of maleate and fumarate are given by following equations: The out of plane vibration of CH for maleate appeared at slightly lower frequency, i.e. at 675 cm-1 due to steric hindrance. It was noted that the increase of the ratio of maleate to saturated acid in the polyester enhances the conversion from maleate to fumarate due to coiling tendency of the chain and causing steric compression. This tendency was also shown by phthalic anhydride based polyesters due to ortho carboxylic group compared with adipic acid and isophthalic acid. It is evident from more conversion from maleate to fumarate in case of phthalic anhydride based polyesters than that of isophthalic acid and adipic acid based polyesters.In case of bisphenol-A based polyesters, low conversion from maleate to fumarate took place, because of less coiling of between the two segments of the chain which are phenyl groups associated through carboxyl group of maleate. Conversion was more pronounced in polyesters based on 2.2-di-(4-hydroxy-3.5-dibromophenyl) propane and 2.2-di-(4-hydroxy-3.5-dichlorophenyl)-propane due to steric hindrance. An alternative explanation for more conversion from maleate to fumarate in case of halogenated bisphenol based polyesters may be due to catalysing effect of the small amount of halogen evolved during polycondensation. Similarly in chlorendic acid (1.4.5.6.7.7-hexachloro-5-norbornene-2.3-dicarboxylic acid) based polyesters, the isomerisation from maleate to fumarate increases as the chlorendic acid content in the polyester increases. In this case catalysing effect of chlorine evolved during polycondensation may be more effective because dissociation of halogen from non-aromatic system is easier than from aromatic system.
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