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  • 1
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Organometallic Chemistry 51 (1973), S. 353-363 
    ISSN: 0022-328X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Organometallic Chemistry 64 (1974), S. 245-254 
    ISSN: 0022-328X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Organometallic Chemistry 64 (1974), S. 255-263 
    ISSN: 0022-328X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1435-1536
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 14 (1985), S. 295-300 
    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 Model networks prepared from polyoxypropylenetriols (PPT) and diphenylmethane diisocyanate (MDI) in an excess of NCO groups were found to contain unusually small amounts of sol, ws, and to have high values of the equilibrium modulus, suggesting an additional crosslinking, probably due to the formation of trifunctional allophanate crosslinks. A comparison of the ws values with the theory of branching processes in which the formation of both urethanes and allophanates is considered allowed us to determine the possible extent of the allophanate reaction, and to calculate the concentration of elastically active chains contributed by PPT and allophanate crosslinks.
    Type of Medium: Electronic Resource
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  • 7
    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 dynamic mechanical behaviour of fully cured off-stoichiometric epoxy systems prepared from poly(oxypropylene)diamine (Jeff D-400) or -triamine (Jeff T-403) and diglycidyl ether of Bisphenol A (DGEBA) with initial ratios of reactive amine (NH2) and epoxide (E) groups, r H= (2[NH2])/[E] ranging from 2.4 to 4.3 was investigated in the gelation threshold region. The evolution of the dynamic behaviour of two stoichiometric samples with r H= 1 with reaction time, t r , was also studied. The critical ratios for gelation, r c H, of fully cured samples were determined from extraction experiments (r c H= 2.54 for Jeff D-400/DGEBA and r c H= 4.15 for Jeff T-403/DGEBA systems, respectively). For both stoichiometric critical gel (CG) structures obtained by changing the curing time t r , a power-law rheological behaviour (G′∼ G″∼ωn, G′ and G″ are the storage and loss moduli, respectively, ω is angular frequency and n is a critical exponent) with the loss tangent, tan δ= G″/G′ independent of frequency, was found. On the other hand, both CG off-stoichiometric systems with r c H ratios show a small dependence of tan δ on ω, so that the critical power-law behaviour is not exactly obeyed. More complex CG structure in these samples, formed due to differences in the structure growth process, was suggested to account for violation of the power-law behaviour.
    Type of Medium: Electronic Resource
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  • 8
    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 copolymer of 2-(2-carboxybenzoyloxy)ethyl methacrylate (CEM) with butyl methacrylate (BMA) (BMA/CEM = 40/60 wt.) and terpolymers CEM/BMA/ 2-hydroxyethyl methacrylate (HEMA) ((BMA + HEMA)/CEM = 40/60 wt.; HEMA/BMA = 35/5, 30/10, 20/20 and 10/30) were prepared by emulsion radical copolymerization in water in the presence of sodium dodecyl sulfate and their dynamic mechanical behaviour was investigated as a function of the degree of neutralization α. Main attention was devoted to the transition from swollen particles to physical gel with increasing degree of neutralization and to the structure of formed hydrogels. From the results it followed: (a) the transition from swollen particles to the gel state occurs in a narrow neutralization interval at α∼ 0.45 for BMA/CEM copolymer; increasing the HEMA content shifts the transition to lower α values; (b) with increasing shear strain γ, the hydrogels passed from the gel to liquid state and this transition at the critical strain γc, was reversible; (c) junctions in the gel state are probably formed by the hydrophobic interactions of the ends of CEM units which form clusters and the junction concentration is independent of the HEMA content and degree of neutralization α; (d) increasing degree of neutralization α and the HEMA content (increasing polarity of the system) stabilizes the junctions and the critical γc values increase; (e) the values of the low-strain storage G′0 and loss G″0 moduli together with critical strains γc did not depend on angular frequnecy ω in the interval 10−1− 10 rad/s.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 24 (1990), S. 619-625 
    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 swelling and mechanical behaviour of networks of copolymers of acrylamide, methylenebisacrylamide and of the quaternary salt-N′,N′,N′-trimethyl-N′-methacrylamido-2-ethylammonium chloride (mole fraction of salt x s =0-0.17) in water-acetone mixtures was investigated. In the range x s 〉0.01 the phase transition was observed; with increasing concentration x s both the extent of transition and the critical concentration of acetone in the mixture, at which the collapse takes place, increase. It was found that, compared with the ester group, the attachment of the positive charge to the main chain through the amide bond increases the extent of transition and decreases the critical acetone concentration. The jumpwise change in the gel volume accompanying the collapse is accompanied by a similar change in the shear modulus of the gel.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 27 (1992), S. 577-583 
    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 swelling and mechanical behaviour of networks of copolymers of acrylamide, methylenebisacrylamide and sodium 2-(2-carboxybenzoyloxy)ethylmethacrylate (mole fraction of salt x s =0–0.2) in water-acetone mixtures was investigated. In the range x s ≥0.01 phase transition (collapse) was observed, with both the extent of the collapse and the critical acetone concentration in the mixture at collapse, a c , increasing with increasing concentration of the salt. A comparison between these results and those obtained for networks with a quaternary ammonium salt led to a conclusion that an exchange of the positive charge of the ammonium salt (N⊕Cl⊖) for the negative charge of the sodium salt (COO⊖Na⊕) in the side chain decreases the critical content of salt necessary for the collapse, X s c , from 0.03 to 0.01, and the collapse takes place at lower concentrations of acetone. The collapse may also take place in a mixed solvent waterethanol; the dependence of network swelling on the concentration of ethanol is roughly the same as that on the concentration of acetone.
    Type of Medium: Electronic Resource
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