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  • Articles  (6,894)
  • Springer  (6,828)
  • Annual Reviews  (66)
  • PANGAEA
  • 2020-2022
  • 1980-1984  (6,894)
  • 1982  (6,894)
  • Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics  (6,894)
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  • Articles  (6,894)
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  • 2020-2022
  • 1980-1984  (6,894)
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  • 1
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 1-12 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 2
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 13-37 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 3
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 61-85 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 4
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 153-187 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 5
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 189-212 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 6
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 261-283 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 7
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 235-259 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 8
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 365-393 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 9
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 87-130 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 10
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 131-151 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 11
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 213-234 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 12
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 285-311 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 13
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 313-345 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 14
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 347-364 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 15
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 395-442 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 16
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Fluid Mechanics 14 (1982), S. 39-60 
    ISSN: 0066-4189
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 17
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 1-21 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 18
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 23-50 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 19
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 51-63 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 20
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 65-80 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 21
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 123-148 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 22
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 103-122 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 23
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 81-101 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 24
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 149-176 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 25
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 177-212 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 26
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 243-269 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 27
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 213-242 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 28
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 271-294 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 29
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 295-321 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 30
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 351-376 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 31
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 323-350 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 32
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 377-398 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 33
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    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 12 (1982), S. 401-413 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 34
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    Polymer bulletin 6 (1982), S. 541-546 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The retraction of stretched molecules explains the intermediate step of relaxation observed at short times with strained polymer melts instead of a single rubberlike plateau. The stress relaxation following a rapid deformation is derived in this zone of the spectrum from the non linear, quasi elastic response of the transient network formed by the system of entangled chains. This method corrects an approximate calculation of the modulus decline in DOI's original treatment of the molecular equilibration process.
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  • 35
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    Polymer bulletin 6 (1982), S. 547-552 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The increased carbohydrate yield after NaOH cooking of wood resulting from NO2/O2 pretreatment is related to the oxidation of reducing sugar end groups to aldonic acid groups during both the pretreatment and the subsequent alkali cook. This leads to a suppressed end-wise degradation during the alkali cook, reflected in a lowered formation of 3-deoxyaldonic and 2-C-methylglyceric acid end groups in competing reactions.
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  • 36
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    Polymer bulletin 6 (1982), S. 553-558 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The curing process in starch adhesives modified with melamine resin can take place by co-condensation or self-condensation. A high degree of co-condensation is required to provide a good water resistance of a cured glue joint. This can be attained by using melamine resins with a high concentration of hydroxymethylamino groups. The reduced effect of the adhesive on storage is due to a degradation of the melamine resin through the elimination of formaldehyde.
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  • 37
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    Polymer bulletin 6 (1982), S. 559-564 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The Raman spectrum of the hexagonal high pressure phase of polyethylene was measured at 5.2 kbar and 240 °C, using a hydrostatic high pressure cell. The spectrum is largely identical to that obtained for the melt. This result indicates that the conformational short range order in the hexagonal phase remains melt —like and is not modified by the overall straightening of chains.
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  • 38
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    Polymer bulletin 6 (1982), S. 565-570 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary It has been found that the three-phase heterogeneous reaction of propane sultone with hydrolyzed macroporous glycidylmethacrylate copolymers in an aqueous alkaline medium proceeds to a higher degree in presence of phase transfer catalyst. The best results were obtained using tetra(n-butyl)ammonium hydroxide. An important finding is the increase in the degree of transformation of the reaction in flow arrangement compared with the batch procedure. The influence of phase transfer catalyst is also more effective. The reaction is discussed with respect to the properties of the products, i.e. of the overall and surface contents of groups introduced into the reaction, of the specific surface area and specific pore volume of sulfopropylated copolymers.
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  • 39
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    Polymer bulletin 6 (1982), S. 571-576 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The initiation effect of ammonia on the polymerization of isobutylene in the presence of VCl4 has been revealed. The polymerizations were carried out in the dark without solvent and in heptane solution in the temperature range between 263 and 198 K, where the molecular weight of the polymer increased linearly with decreasing temperature (log Mη against 1/T). The polymer yield depended on the molar ratio of ammonia to VCl4 and was highest at 1∶1, but the polymerizations proceeded also at a molar ratio higher than 1. At NH3/VCl4 = 1 the polymerization rate increased with VCl4 concentration and with decreasing temperature.
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  • 40
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    Polymer bulletin 6 (1982), S. 243-249 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Chelate polymers obtained from bis(2,4-dihydroxybenzaldehyde) M2+ (M = Fe2+, Co2+, Ni2+, Zn2+) with organic acid chlorides were synthesized and characterized by elemental a-nalysis, magnetic and electric measurements, spectral and thermogravimetric studies.
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  • 41
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    Polymer bulletin 6 (1982), S. 235-241 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary In this paper is decribed a new method for determining copolymerization reactivity ratios r by using high resolution gel permation chromatography. The system of monomers is a new one involving a macromer. Separation of each monomer, copolymer and solvent allows calculation of concentration of reactants and products, so as the copolymer molecular weight distribution. Three different methods were used to interprete copolymerization experiments, at various feed compositions, and in function of conversion, in minimizing errors on peak surface area. The conventional methods were used to calculate r and evaluate their accuracies.
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  • 42
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    Polymer bulletin 6 (1982), S. 251-257 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract The present investigation concerns the synthesis of statistical networks similar to vulcanized rubber. We have used liquid precursor polymers: polybutadiene (PB) and polyisoprene (PI) with telechelic siloxanes. The reactivity of the polydienes can be classified as follows: PB units 1,2 ⋙ PI units 3,4 ⋙ PI units 1,4 ≃ 0. The network formation is a function of the ratio R = nb, of pendent double bonds/nb. of ≃ SiH. For R ≃ 1 the networks are rather hard and brittle, for 8 ⩽ R ⩽ 10 they are soft and elastic, whereas for R ≃ 16 the gels obtained are very soft and sticky.
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  • 43
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    Polymer bulletin 6 (1982), S. 299-303 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The replacement of the chlorine atoms of chloromethylated polystyrenes by carboxyl groups via reaction with disodium tetracarbonylferrate and subsequent treatment with an oxidizing agent is described.
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  • 44
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    Polymer bulletin 6 (1982), S. 305-308 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Synthetic glycolipids have been prepared by coupling of (a) aliphatic amines with lactone derivatives, or (b) fatty acids with amino derivatives of mono- and disaccharides via amide linkage. The aliphatic chain was varied with respect to the chain length and to its chemical composition (fluorination, functional end group). The influence of the glycolipid structure on the monolayer properties was investigated. Stable films are obtained with most of the products mainly due to strong interactions by hydrogen bonds in the subphase. Polymeric films may be produced by polycondensation in the subphase using particular crosslinking agents for the carbohydrate head group.
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    Polymer bulletin 6 (1982), S. 309-314 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Electro-optical behaviour of a liquid crystalline polymer- poly{1-[6-[4-N-(4-cyanophenyl)iminomethylphenoxy] hexyloxycarbonyl] ethylene}- is studied A sharp change of the optical properties measufred in crossed polarizers under the cooling of the preliminary oriented sample in an electric field is observed. The effect is explained from the viewpoint of the electric field induced cooperative structure transition.
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  • 46
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    Polymer bulletin 6 (1982), S. 321-326 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Solution properties of trimethylcellulose-poly(oxytetramethylene two and star block copolymers with defined molecular weights are reported. The solubility behavior of the concerned block copolymers is mainly governed by the solubility of the trimethylcellulose blocks. The solubility parameters for TMC and POTM indicate that both polymers are incompatible with each other. This is confirmed by the appearance of phase separation in concentrated solutions of corresponding blends even in nonselective solvents. Intrinsic viscosities of the block copolymers are reported and compared to corresponding polymer blend solutions.
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    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Reaction of different furanes (2,3- and 2,5-dihydrofurane, tetrahydrofurane, furane) were examined in the presence of Cr(II) surface compounds on silicagel as catalyst. In every case poly (2,3-dihydrofuran) was obtained. The products of the occuring hydrogenation, dehydrogenation and isomerisation reactions were detected by GC and NMR spectroscopy. A mechanism for the reactions is proposed.
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  • 48
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    Polymer bulletin 6 (1982), S. 327-333 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The effect of Lewis acids on various ethylene-propylene co- and terpolymers has been investigated in the mixing chamber of a Brabender Plastograph at 180°C. Fast degradation of the polymers was observed upon the addition of Lewis acids. Terpolymers containing unsaturations undergo crosslinking: the structure of the third monomer (diene) determines the rate of crosslinking and the characteristics of the crosslinked materials.
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    Polymer bulletin 7 (1982), S. 289-294 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Graft copolymers composed of poly(methyl methacrylate) branches and different backbones of poly(fluoroalkyl acrylate(FA)-co-methyl methacrylate(MMA)), poly (hydroxyethyl methacrylate(HEMA)-co-MMA), and poly(FA-co-HEMA) were prepared by macromonomer technique to study their application as a surface modifier for PMMA films. Contact angle of water droplet on PMMA film specimens containing various amounts of these graft copolymers cast on glass slides from THF solution was found to change considerably with the graft copolymer concentration, depending on their backbone component. And there was considerable difference in contact angle between air and glass side of the film surfaces. These results were considered in terms of the surface accumulation of graft copolymers during the solvent evaporation.
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    Polymer bulletin 7 (1982), S. 309-316 
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    Notes: Summary An ultra-high strength polyethylene fiber with an initial tensile strength at break of 3.0 GPa, was irradiated at room temperature under vacuum by means of 60Co γ-radiation. Gelcontent and equilibrium volume degree of swelling of the gelfraction, were determined as a function of dose. From a plot of the effective network chain density versus dose, it was concluded that the fiber contained about 2 entanglements per number average molecule. Furthermore, a crosslinking efficiency of 0.33 crosslink per 100 eV of absorbed energy was found.
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    Polymer bulletin 7 (1982), S. 323-330 
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    Notes: Summary A numerical regression method, assisted by a least squares technique, is proposed to obtain thermodynamic and hydrodynamic parameters of polymer molecules via a direct comparison between experimental data and theoretical functions. This comparison is independent of the number of the experimental variables. The method also enables to decide if a selected set of theoretical equations fits satisfactorily the experimental results.
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    Polymer bulletin 7 (1982), S. 317-321 
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    Notes: Summary An alternative procedure to examine the nature of the end product of nitric-acid-treated bulk polyethylene involving the measurement of the diamagnetic susceptibility is reported. This simple non-destructive method complements previous results obtained by means of IR spectroscopy. Thus after selectively removing the surface layer of the polyethylene lamellae with nitric acid (t 〉 50h) the diamagnetic susceptibility substantially decreases to values which are consistent with tilted paraffinic chains terminated by carboxyl groups including -NO2 groups in a 4∶1 ratio.
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    Polymer bulletin 7 (1982), S. 331-336 
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    Notes: Sumnary The glass transition temperatures of 2,4-diphenylpentane, 2,4,6triphenylheptane and 2,4,6,8-tetraphenylnonane are shown to follow the relation Tg = 325 − 2.64 × 104/Mn where Mn is the molecular weight. 2,4-diphenylpentane-2,4,6-triphenylheptane mixtures exhibit only one glass transition temperature which follow the relation Tg = (1 − ω2) Tg1 + ω2 Tg2 where ω2 is the weight % of 2,4-diphenylpentane. The configurational structure of these polystyrene model molecules is shown to slightly influence the Tg's values.
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    Polymer bulletin 7 (1982), S. 337-344 
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    Notes: Summary The synthesis of the novel graft-block copolymer poly[chloroprene-g-(isobutylene-b-α-methylstyrene)], i.e., a polychloroprene backbone carrying isobutylene/α-methylstyrene block copolymer branches, is described. The synthesis was accomplished by exploiting detailed insight into the mechanisms of initiation of isobutylene and α-methylstyrene polymerization, and termination of isobutylene polymerization.
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    Polymer bulletin 7 (1982), S. 353-359 
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    Notes: Summary High resolution carbon−13 nuclear magnetic resonance spectroscopy is used to study the structure of N-amide and N-sulphonamide derivatives of polydiallylamines and shows that these have the poly(3,4-pyrrolidinediylethylene) structure common to most polydiallylamines, not the previously reported poly(3,5-piperidinediylmethylene) structure.
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    Polymer bulletin 7 (1982), S. 345-351 
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    Notes: Summary Styrene polymers containing pendant p-vinyl or p-oxirane functionalities on some of their aromatic rings have been prepared in excellent yields by chemical modification of chloromethylated polystyrene or carboxaldehyde-substituted polystyrene under phase transfer catalysis. The polymers containing pendant vinyl groups were obtained by Wittig reactions with aqueous formaldehyde while the polymers with p-oxirane pendant groups were obtained by reaction of the carboxaldehyde polymer with trimethyl sulfonium chloride or epoxidation of the p-vinyl substituted polymer.
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    Polymer bulletin 7 (1982), S. 361-367 
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    Notes: Summary A polymeric reagent, polystyryldiphenyl-phosphine tetrahydroborate copper, has been prepared by chemical modification of cross linked polystyrene using a fourstep reaction sequence involving a ligand exchange reaction for the binding of cuprous chloride to the phosphine resin. The reagent is very effective in the reduction of acid chlorides to aldehydes and can be regenerated easily without loss of activity.
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    Polymer bulletin 7 (1982), S. 369-376 
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    Notes: Summary A new procedure for the preparation of model polymer networks having an inhomogeneous distribution of crosslinks has been developed. Emulsion polymerized polystyrene/divinylbenzene microspheres, of uniform particle size, are swollen with styréne monomer, which is later polymerized in situ. The resulting network consists of discrete sites of crosslinked material dispersed in an interpenetrating matrix, and is suggested as a model for the nodular morphology which has been observed in some epoxy networks. The results of initial studies showing the effects of nodule size and concentration on the fracture toughness of the glassy networks are presented.
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    Notes: Summary Kennedy's inifer technique has been modified and used for the preparation of α,ω-dichloro polyindene (PInCl2). This telechelic has subsequently been used as initiator for the cationic isobutylene polymerization in conjunction with AlEt2-Cl coinitiator. The resulting materials have been characterized by fractionation and GPC investigations.
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    Polymer bulletin 7 (1982), S. 391-394 
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    Notes: Abstract Controlled enzymatic hydrolysis of cuprammonium and various types of viscoses was undertaken to gain some insight into the heterogenity of the structure from the surface to core. Electron microscopic study of the hydrolysed samples at various stages of hydrolysis, also gives general idea of the morphological differences in these regenerated celluloses. The difference in the physical and especially the mechanical properties of the different types of these fibres can now be more definitely correlated with their structure.
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    Notes: Summary Interpolymer complex formation between poly(styrene-b-ethylene oxide) block copolymers (PS-PEO) and poly(acrylic acid) (PAA) has been studied by viscometry using THF-water mixture of several compositions as solvent. Unlike alternating and random copolymers, composition of the complex formed between (PS-PEO) and PAA does not seem to be affected by the molecular characteristics of the copolymer and the solvent composition. However the nature of the reduced viscosity curves during complex formation was found to be dependent on solvent composition and this has been interpreted in terms of preferential solvation, conformation and micellization of the block copolymer molecules.
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    Polymer bulletin 7 (1982), S. 395-399 
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    Notes: Summary Radiation grafting onto polyethylene tubes was carried out using vinyl monomers carrying functional groups to which antibodies against thyroxine were covalently bound. The grafting tests were carried out in different solvents varying the dose rate and irradiation time so that the grafting yield could be effectively controlled. Coupling via an active ester using 1-hydroxybenzotriazole shows optimal results with a retention of biological activity of over 70%.
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    Polymer bulletin 7 (1982), S. 409-412 
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    Notes: Summary It is shown, that melting of chain molecules can be described as a double process: 1) a conformational transition, where the “liquid” molecule conformation is created and 2) the “real” melting caused by the cooperative insertion of dislocations, 3-dimensionally arranged in dislocation walls. This melting concept is shown to be valid in atomic crystals as well as in low molecular crystals and in polymers, too.
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    Polymer bulletin 7 (1982), S. 413-416 
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    Notes: Summary The meander model of polymer melts assumes nearly parallel packing of molecular chains and therefore invites to describe shear deformation processes by “dislocation” motion in analogy to metals. Examination of the glass relaxation data for 12 amorphous polymers leads to reasonable values for the energy and the Burgers vector of segment dislocations which are also consistent with thermal properties of the glass transition.
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    Polymer bulletin 7 (1982), S. 401-408 
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    Notes: Abstract An automatic method and apparatus for continuous monitoring of vinyl chloride suspension polymerization was developed and built, which enables a parallel measurements of attenuation changes and velocity of ultrasonic propagation in frequency range from hundreds of kHz to units of MHz and in dynamic range greater than 60 dB. The results of automatic measurements were compared and tested by previous results obtained manually by means of MATEC Model 6000/755 ultrasonic comparator and have showed many substantial advantages of ultrasonic attenuation measurements for checking through the suspension polymerization of vinyl chloride e.g. possibility of indication of very fast phase changes during the process as well as the prediction of the PVC particles final morphology properties including eventual undesirable polymerization courses.
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    Polymer bulletin 7 (1982), S. 481-487 
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    Notes: Summary In this study the changes in the width of the derivative NMR absorption line and the second moment as the function of temperature were investigated for typical urethane elastomers. The polymers crosslinked only by allophanate and biuret bonds as well as modified by the presence of carbon-carbon and ionic bonds were used. It has been found that carbon-carbon and ionic crosslinking bonds cause considerable changes in the glass transition temperature.
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    Polymer bulletin 7 (1982), S. 497-504 
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    Notes: Summary The poling of biaxially stretched poly(vinylidene fluoride) (PVDF) films which have been metallized on both sides results at the poling temperature of 115 °C and the poling field of 400 MV/m in almost complete conformational change from T-G-T-¯G to the trans conformation as well as in a residual polarization of at least 11×10−2 C/m2. The transition temperature Tf of the field-induced conformation transformation in the crystalline regions is found to be Tf = 75 °C. The thermally stimulated decrease of polarization proceeds gradually and is not characterized by a defined Curie point.
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    Notes: Summary Photoconductivity of organic polymers can be greatly enhanced and extended into the visible region by the addition of small amounts of additives, such as electron acceptors and dyes. These effects can be explained as the result of photoredox processes and as the result of an influence of local fields of donor-acceptor complexes upon the photogeneration of charge carriers.
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    Polymer bulletin 7 (1982), S. 489-495 
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    Notes: Summary Autooxidation of low density polyethylene has been studied in melt and in 1,2,4-trichlorobenzene solution. The kinetics of oxygen-absorption, concentrations of hydroperoxides, carboxyl, and other oxo groups and average number of scissions have been investigated. It has been found that the main features of the oxidative processes in solution and in melt do not differ significantly. However, the concentration of hydroperoxides as a function of conversion and the dependence of the maximum concentration of hydroperoxides on temperature make exception. There is a very good agreement between average number of chain scissions and carboxyl groups and this is independent of phase, concentration, temperature, and conversion. From one mole consumed oxygen approximately 0.6 ÷ 0.7 mole remains in the polymer backbone in the form of oxygen-containing functional groups. The ratio of average chain scissions to the formed carbonyl groups is 1∶5, i.e., functional groups form both at the chain ends, in consecutive reactions after the scission, and along the polymer chain.
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    Polymer bulletin 8 (1982), S. 1-8 
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    Notes: Summary The activating effect of halogens on the reactions of sulfur with phenol, guaiacol and o-cresol is investigated. As expected bromine has a stronger effect than chlorine, but in both cases oligomeric and polymeric poly(hydroxiphenylene sulfides) containing halogens are formed. When o-cresol is used as monomer, CH2-S-CH2 bonds are apparently formed when the reaction time is increased. The products are investigated by IR-spectroscopy, gel permeation chromatography, elementary analyses and the temperature at which the material turns to a resinous product is given.
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    Notes: Summary Measurements are reported on thermally stimulated discharge current in methacrylonitrile — styrene copolymer films. The values of activation energy and relaxation times were calculated.
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    Polymer bulletin 8 (1982), S. 9-13 
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    Notes: Abstract Blends of poly(ɛ-caprolactone) with either head-to-head or head-to-tail poly (vinyl chloride) were prepared by solvent casting in the form of films and their glass transition temperatures were determined by DSC analysis. The DSC scans of the blends of both poly(vinyl chloride) isomers were very similar. For blends containing 25% and 50% of poly(ɛ-caprolactone), a single transition step, a Tg, was observed, whereas for a blend containing 75% of poly (ɛ-caprolactone) three transition steps were observed, one glass transition and also a crystallization and a melting transition.
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    Notes: Summary Linear and three-arm star tosyl-telechelic polyisobutylenes (i.e., PIB's carrying two and three p-toluene-sulfonic acid ester end groups, respectively) have been synthesized and characterized by a variety of techniques. Subsequently these prepolymers were used as macroinitiators for the ring opening polymerization of 2-methyl-2-oxazoline leading to linear poly(N-acetylethyleneimine-b-isobutylene-b-N-acetylethyleneimine) and three-arm star poly(N-acetylethyleneimine-b-isobutylene). High yields (78–98%) and blocking efficiencies (70–80%) have been obtained. The absence of free polyisobutylene in the product indicates highly efficient initiation of 2-methyl-2-oxazoline polymerization by the tosyl-telechelic polyisobutylene. The less than 100% blocking efficiencies are probably due to chain transfer to 2-methyl-2-oxazoline. Hydrolysis of these block copolymers yielded poly(ethyleneimine-b-isobutylenes).
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    Polymer bulletin 8 (1982), S. 21-24 
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    Notes: Summary Protonation of the rodlike polybenzobisoxazoles (PBO) and polybenzobisthiazoles and their model compounds in acidic media will have significant effects on their solubility, solution behavior, geometry, and conformational characteristics. Experimental studies on the cis-PBO model compound suggest that the aromatic heterocyclic group can accept up to four acidic protons, first at each of the two nitrogen atoms then at the two oxygen atoms. In this study geometry-optimized CNDO/2 calculations were carried out on the cis-PBO model compound to determine the order of successive protonation, estimate differences in proton binding energies, and provide information on the effects of successive protonation on the geometry and charge distribution. The results indicate that protonation occurs in the order nitrogen, nitrogen, oxygen, oxygen, which is consistent with the greater bascity of nitrogen relative to oxygen. The difference in energy between initial protonation at nitrogen versus oxygen is ca. 60.7 kcal mol−1. Second protonation is preferred at the other nitrogen rather than at the more distant oxygen by nearly the same amount, suggesting that energetically the initial protonation at the nitrogen has a negligible effect on subsequent protonation and that the two oxazole moieties are highly insulated from each other. Repulsive Coulombic interactions between the acidic protons have a negligible influence on whether the second protonation occurs at the nitrogen or the oxygen considered. Coulombic effects will in fact slightly favor at the nitrogen since, despite its closer proximity to the nitrogen first protonated, protonation there yields a more delocalized and hence less repulsive charge distribution than at the oxygen.
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    Polymer bulletin 8 (1982), S. 39-45 
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    Notes: Summary NMR techniques have been used to characterize the transitions with temperature of a very thin film of a copolymer FEP wich had covered the walls of a maser cavity. Several points on the frequency-temperature chart have been obtained from a study of the temperature variation of the second moment and of the relaxation times T1 and T1ϱ. They confirm that the transitions observed in the temperature dependence of the factors which control the maser stability are associated to very low frequency molecular motions.
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    Notes: Summary Keeping in view the prospects of biodegradable polymers, a polymer was synthesized by the condensation of carboxy-terminated polybutadiene (CTPB) of Mn∼-5000 with glycerol and tested for its microbial susceptibility. The results of end group estimations and viscosity measurements indicated a quantitative reaction between the two reactants under experimental conditions. The clear-zone method was employed in this investigation to test biodegradability. Two strains of Serratia and three strains of Staphylococcus did show a clear zone surrounding the colony. However, the microbial growth was found to diminish after 4 or 5 days.
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    Polymer bulletin 8 (1982), S. A1 
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    Polymer bulletin 8 (1982), S. 487-494 
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    Notes: Summary 75.4 MHz 13C NMR CP/MAS spectra allowed the quantification of the secondary structure of (γOMe-L-Glu)n and (γOBzl-L-Glu)n. (OMe-L-Glu)n contains α-helix and β-sheet structures the ratio of which varies considerably with the average degree of polymerization ( $$\overline {{\text{DP}}} $$ ) of the samples and with the nature of the reaction medium. At $$\overline {{\text{DP}}} $$ ≥20 (γOBzl-L-Glu)n contains more than 95% α-helix structure regardless of $$\overline {{\text{DP}}} $$ and reaction medium. The difference between both polyglutamates is explained by different molecular weight distributions resulting from aggregation and precipitation of oligo (γOMe-L-Glu)n in the ß-sheet form.
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    Polymer bulletin 8 (1982), S. 495-502 
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    Notes: Summary Various copolypeptides with a two block sequence are prepared by batchwise copolymerizations of amino acid N-carboxyanhydrides (NCAs) using primary amines as initiators. An α-helix forming amino acid and a ß-sheet forming amino acid were combined in the two blocks and the mutual influence of the two secondary structures was investigated by means of 13C nmr crosspolarization magic-angle spinning (CP/MAS) spectra. It was found that the second (succeeding) block adopts partially the secondary structure of the first block.
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    Polymer bulletin 8 (1982), S. 503-510 
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    Notes: Summary By variable temperature proton enhanced magic angle spinning 13C NMR below Tg individual conformational diads could be resolved for glassy phase segments in semicrystalline erythrodiisotactic poly(1,2-dimethyltetramethylene). An assignment based on γ-shift increments associated with antigauche conformational transitions is given. In addition an improved interpretation of conformational effects in the glassy phase solid state spectrum of amorphous threodiisotactic poly(1,2-dimethyltetramethylene) is presented.
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    Polymer bulletin 8 (1982), S. 511-517 
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    Notes: Summary The sulfonation of the model compounds of the structural units of the polysulfones and bis phenol A polyethersulfones has been conducted up to completion using SO3 in a dichloroethane solution at room temperature. Whatever the initial structure may be, only one sulfonic group per aromatic ring can be attached. Water soluble polymers with the same degree of sulfonation can be prepared, without chain scission.
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    Polymer bulletin 8 (1982), S. 527-534 
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    Notes: Summary Results are described of TSD- and TSP-measurements of Poly (Phenylquinoxaline) in dependence on the degree of annealing and on the polarizing field strength. Seven relaxations regions are investigated and discussed. Electronic and ionic space charge regions are observed and discussed in detail. It is shown that dielectric losses in polymers do not result from dipolar processes only, but also from translational motion of charge carriers.
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    Polymer bulletin 8 (1982), S. 519-525 
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    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Equilibrium swelling measurements in the system polystyrene — cyclohexane — acetone within the temperature range from 288 to 323 K confirm the conclusion drawn from light scattering investigations (Schuster, R. H., Cantow, H.-J. and Klotz, S., 1982) that the system exhibits the characteristics of cosoivency. A thermodynamic analysis of the experimental data following the Flory-huggins-rehner one-parameter equation in terms of χ, χH and χS is compared with that (Cantow, H.-J. and Schuster, R. H., 1982) based on the free energy two-parameter equation proposed by Koningsveld and Kleintjens. Thus, an unequivocal interpretation of the swelling thermodynamics of the ternary system could be reached, irrespective crosslink density of the network. The cosoivency effects are discussed in relation to the heat of mixing. The conclusion has been proved that the cosoivency is caused by breakdown of acetone clustering by dilution with cyclohexane.
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  • 84
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    Polymer bulletin 8 (1982), S. 535-542 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Siloxane-urea copolymers were synthesized from MDI and α, ω-bis(aminopropyl)polydimethylsiloxane of different molecular weights by solution polymerization, using 2-ethoxyethyl ether as the solvent. Chain extenders were also employed in some reactions. Formation of urea linkages were followed by FTIR spectroscopy. The products were characterized by GPC chromatography and intrinsic viscosity measurements. Thermal (DSC) and thermomechanical (TMA) characterization of the products were also carried out. The results indicate the formation of novel, strong multiphase elastomeric siloxane-urea copolymers.
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  • 85
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    Polymer bulletin 8 (1982), S. 543-550 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The mechanical behavior of new siloxane-urea segmented copolymers, based on amino terminated poly(dimethylsiloxane) oligomers of about 1000 to 4000 〈Mn〉 and 4,4′ -diphenylmethane diisocyanate (MDI), has been investigated. These segmented block copolymers appear to form microphase texture and display mechanical behavior which is in some ways comparable to filled silicone elastomer systems as well as segmented polyurethanes. Preliminary studies of the effect of hard segment content on mechanical properties are also reported. As expected, the stress-strain behavior reflects composition changes.
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  • 86
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    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary α, ω-Di(hydroxy)polyisobutylene was converted to the corresponding α,ω-di(allylether)- and α,ω-di(allylphthalyl)polyisobutylene by reacting the diol with allyl bromide in the presence of alkali and tetrabutylammonium bisulfate phase transfer catalyst, and monoallyl phthalic acid chloride in the presence of 4-N,N-dimethylaminopyridine, respectively. The reaction conditions were defined by suitable model experiments. IR and 1H-NMR analysis of the reaction products indicates quantitative conversions.
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  • 87
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    Polymer bulletin 8 (1982), S. 557-562 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The synthesis of α-phenyl-ω-t-chloropolyisobutylene PhPIB-Cl t by the use of the cumyl chloride/BCl3/isobutylene minifer system has been accomplished. This asymmetric telechelic prepolymer possesses exactly one phenyl head group and one t-chloro end group. The molecular weight of Ph-PIB-Cl t can be readily controlled by the [I]O/[M]O ratio in a refluxing system. Experiments with other minifers, i.e., p-methylcumyl chloride, p-chlorocumyl chloride, α-methylbenzyl chloride and benzyl chloride have also been carried out and the results discussed in terms of carbenium ion stabilities.
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  • 88
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    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The synthesis and quantitative end group characterization of bisphenol- and trisphenol-polyisobutylenes are described. These new telechelic prepolymers consist of a linear or a threearm star polyisobutylene (PIB) carrying exactly two or three phenol termini, respectively. The syntheses were accomplished by quantitative Friedel-Crafts alkylation of phenol by olefin- and/or tert.-chlorine-telechelic PIB's and characterization involved 1H NMR, UV and GPC techniques. These materials combine the chemical versatility of the- C(CH3)2C6H4OH end group with the attractive physical-chemical properties of the rubbery PIB chain.
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  • 89
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    Source: Springer Online Journal Archives 1860-2000
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    Notes: Summary Glycidyl ethers of bisphenol- and trisphenol-polyisobutylenes have been prepared, characterized, and cured with amines to new flexible epoxy resins. The synthesis of these glycidyl ethers involved quantitative condensation of epichlorohydrin with phenol-capped linear or three-arm star polyisobutylenes. Proton NMR analysis of the model compound monoglycidyl ether of 2,4,4-trimethyl-2(p-hydroxyphenyl)pentane and the corresponding glycidyl ethers of phenol-capped polyisobutylenes showed the presence of epoxy end groups. According to 1H NMR spectroscopy and titration data the number-average terminal epoxy functionality is close to the theory, i.e., two or three, for the linear and three-arm star products. Curing these new epoxides with triethylene tetramine resulted in transparent, non-tacky flexible films.
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  • 90
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    Polymer bulletin 8 (1982), S. 579-584 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Two new methods of calculation of memory functions, governing the exciton propagation, in linear finite chains and consequent calculation of the quantum yield of the exciton transfer, observable in e.g. experiments on monomer and excimer luminiscence, are reported. Illustrative numerical results are shown to discuss the effect of inhomogeinities, boundaries and relative magnitudes of relevant parameters on the result.
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  • 91
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    Polymer bulletin 8 (1982), S. 585-591 
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    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Derivatives of poly(oxyethylene) with chlorine and aldehyde functions have been prepared by chemical modification in an one-step and two-step reaction respectively with thionyl chloride and 4-hydroxy benzaldehyde in excellent yields. The functionality of these important intermediates has been investigated spectroscopically and demonstrated by chemical conversion of the terminal groups.
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  • 92
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    Polymer bulletin 8 (1982), S. 47-54 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract Three-arm star polyisobutylene ionomers (¯Mn=8800) with terminal ∼SO3 ⊖ M⊕ (M⊕=K⊕ or Ca2⊕) groups were synthesized and their mechanical properties investigated. Compression molded films displayed high elongations, i.e., ∼-1000% for Ca2⊕ ionomers with lower values for the K⊕ counterions. Strain induced crystallinity was observed at higher elongations. Mechanical properties in general compared favorably with conventional covalently linked rubbery networks and were comparable and in some cases superior to EPDM-based ionomers carrying randomly distributed ∼SO3 ⊖ M⊕ groups.
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  • 93
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The electrical properties of polymer films prepared from tetramethylsilane (TMS) and the mixture of TMS and oxygen by glow discharge polymerization were investigated in connection with the chemical structure of the polymers. The polymer films showed two different electrical properties which depended on the strength of electrical field. Under the electrical field of less than 104 V/cm, the polymers showed ohmic behaviour, and their resistivity was approximately 1014 Ω · cm being independent of the chemical structure of the polymers. Under the electrical field of above 104 V/cm, non-ohmic behaviour was observed, and the current increased exponentially with increasing of the applied field. To explain this enhanced current the contribution of the Poole-Frenkel emission was assumed. The dielectric breakdown of the polymer films (1000–5000 angstroms) occured at the electrical field as high as 3 MV/cm. This indicates that these thin films may be deposited on substrates without pinhole.
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  • 94
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    Polymer bulletin 8 (1982), S. 55-61 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The synthesis of appropriate monomers bearing alkylidyne tricobaltnonacarbonyl cluster or sulfido tricobalt heptacarbonyl cluster is described. Organometallic copolymers are obtained by free-radical copolymerisation with other vinyl monomers. Direct metallation of macromolecules containing the dithioester or the thioamide functional groups was also studied. We show that the copolymerisation method is more convenient for the synthesis of pure materials containing a variable amount of definite cluster units. The potentiality of these new organometallic polymers with regard to homogeneous catalysis and for the modification of electrode surfaces is also discussed.
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  • 95
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    Polymer bulletin 8 (1982), S. 63-67 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The validity of the copolymer composition equation for the copolymerization of macromers with small monomers for the preparation of graft copolymers has been examined. The reactivity ratios of high molecular weight macromers r1 cannot be determined experimentally with sufficient accuracy whereas those of small monomers r2 may be calculated by r2=ln(1-p2)/ ln(1-p1), where p1 and p2 are the respective conversions of the macromer and small monomer. A single experimental datum obtained even at high conversions may be used. The error of the method can be readily calculated.
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  • 96
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    Polymer bulletin 8 (1982), S. 75-79 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Effect of the hydrophobicity of the polymer matrix on the immobilization of lipase by radiation polymerization was studied. The enzymatic activity of the immobilized enzyme composites was affected by hydrophobicity, and optimum hydrophobicity existed for the enzyme reaction at the surface of the immobilized enzyme composites. Furthermore, the enzymatic activity was affected by monomer concentration. In the immobilization using polyethyleneglycole diacrylate monomers, the enzymatic activity increased with increasing number of ethyleneglycole unit in the monomer molecule.
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  • 97
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Polyisobutylene-based polyurethane networks have been synthesized by crosslinking polyisobutylene glycols with tri-phenylmethane triisocyanate and their gas permeability, water absorption, hydrolytic stability, and air oven aging characteristics was examined by ASTM methods. The preparation of the polyurethane sheets is described. The oxygen permeability of polyisobutylene-based polyurethanes is lower than that of vulcanized butyl rubber and their water absorption is negligible. The hydrolytic stability of these new polyurethanes is outstanding and their mechanical properties (tensile strength, modulus, elongation) remain practically unchanged after four days of exposure to 85° steam. Similarly, air aging for two days at 128° affects little mechanical properties.
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  • 98
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    Polymer bulletin 8 (1982), S. 95-99 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary It was found that the drift mobility of carriers in tetracene and p-quaterphenyl polycrystalline layers is dependent on electric field. A simple model to explain the dependence is presented in this paper.
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  • 99
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Storage and chemical stability of TCNQ anion radical salts with polycations containing sulfur atoms in the main chain was investigated as a function of time and solvent used for their synthesis. The UV and visible light absorption spectra of solution have evidenced that the storage of these polymeric salts at room temperature results in the appearance of a new absorption band asscribed to α,α-dicyano-p-toluoylcyanide anion. It was found that the ageing reaction depends on the residual solvent as well as on the method of synthesis of these complex salts.
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  • 100
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    Polymer bulletin 8 (1982), S. 109-116 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract Aliphatic and partially aromatic alternating polyesteramides were prepared from appropriate bisesteramides and aliphatic diols of various chain length. An investigation of their thermal and viscoelastic behaviour showed that the Tm and Tg values of such polyesteramides are those to be expected for a system with intermediate properties between those of the two homopolymers. A discussion of the experimental Tm values in terms of group contributions is presented.
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