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  • 1
    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 Functionally terminated bisphenol-A polysulfone oligomers were used in the modification of Epon Resin 828/4,4′-diamino-diphenylsulfone (DDS) network system. Phenolic hydroxyl terminated PSF oligomers were first capped with a large excess of bisphenol-A diglycidyl ether or Epon Resin 828 at both ends and then the resulting system was cured with DDS, in a two-step process. During these studies molecular weight and the amount of PSF oligomers incorporated into the network were varied and their effect on the overall properties of the resulting systems were investigated. The capping and curing reactions were followed by using FT-IR and NMR spectroscopy, GPC, HPLC and DSC techniques. As a function of the oligomer molecular weight, SEM studies showed the formation of two-phase structures with ductile PSF particles dispersed in the continuous epoxy matrix. Mechanical characterization and fracture toughness measurements showed a remarkable increase in KIC or gIC values of the modified networks over that of control, without significant loss in the modulus. This work would appear to be one of the first studies where well bonded ductile glassy modifiers have significantly improved the fracture toughness of highly crosslinked networks.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    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.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    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.
    Type of Medium: Electronic Resource
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  • 4
    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 kinetics of the curing reaction of an epoxy resin based on bisphenol-A diglycidylether with a cycloaliphatic diamine, bis(4-aminocyclohexyl)methane, was studied by differential scanning calorimetry. The measurements were performed both under isothermal conditions and as a function of heating rates. The reaction was also followed by determining the Tg of the resin cured for different time intervals at 150°C. The enthalpy of the reaction was derived from these measurements. The rates and extent of cure were determined. The cycloaliphatic amine used for this study was demonstrated to be more reactive than analogous aromatic systems and yet provided rigid networks with a desirably high Tg.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ionic groups incorporated into a polymer have a decided effect on its physical properties. A number of ionomers and polyelectrolytes have been widely applied. In particular, sulfonated bisphenol-A polysulfone (SPSF) has been used as a composite or single-component membrane for the desalination of water. In this article, the synthesis and physical characteristics of sulfonated polysulfone are addressed. A detailed synthesis route is provided and methods that yield determinable levels of sulfonation are described. These ion-containing polymers retain an excessive amount of residual salts, which, of course, are impurities to the system. Therefore, before any analyses were made the polymers were subjected to a thorough soxhlet extraction process with boiling water, which appeared to be quite effective. The degree of sulfonation was assessed by several methods such as 1H NMR and FT-IR. A new 1H NMR method was derived because the method cited in the literature proved to be too inconsistent for our work. The new 1H NMR method used a quaternary ammonium counterion [N(CH3)4]. These methyl protons are easily measured and may be ratioed against the isopropylidene protons in the polymer backbone that act as an internal standard. Characterization of the physical properties of SPSF consisted of water uptake, differential scanning calorimetry (DSC), thermomechanical analysis (TMA), and solubility studies. Its physical appearance and mechanical behavior were improved by the solution procedure. Also addressed were the effects of different counterions (Na+ & Mg++) with SPSFs of low levels of sulfonation. The variation in physical properties between the divalent and monovalent counterions is dramatic, especially when observed by TMA in the rubber plateau above the apparent glass temperature.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 679-704 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of bisphenol A poly(carbonate-ester) copolymers was studied by phase-transfer catalysis and modified interfacial polymerization. Only low molecular weight copolymers were prepared directly from dicarboxylic acids, phosgene, and bisphenol A by an interfacial process that involves the use of pyridine as catalyst, HCl acceptor, and weak base. To avoid the use of tertiary amines, which can be difficult to remove from the polymer products, and to produce higher molecular weight copolymers from the same dicarboxylic acid precursors another synthetic method was developed. This more effective method required careful pH control that was achieved by the selective use of the weak-base potassium carbonate in the first stage of the process. Moreover, elevated reaction temperatures (∼65-70°C) and phase-transfer catalysis were used. The carbonate-ester copolymers prepared by this technique had consistently high intrinisic viscosities, little or no anyhydride microstructure, and higher degrees of ester unit incorporation than those produced by the pyridine-catalyzed method. These copolymers also had glass transition temperatures (Tg) 20-30°C higher than bisphenol A polycarbonate homopolymer. An analytical method for determining quantitatively the amount of ester units in the bisphenol A poly(carbonate-esters) was developed by using Fourier transform infrared spectroscopy (FT-IR). Agreement between this FT-IR method and a quantitative nuclear magnetic resonance (NMR) method was found to be reasonable, especially for copolymers with ester unit percentages lower than 40%.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0272-8397
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Synthesis and free-radical curing reaction of the bisglycidylmethacrylate of bisphenol-A (Bis-GMA) were investigated. Bis-GMA resin was synthesized by reacting Epon 825 with methacrylie acid, followed by characterization using IR and NMR spectroscopy. Various modifiers having reactive double bonds were co-cured with the methacryloxy resins using a free-radical initiator. The networks obtained were compared with a cycloaliphatic amine-cured epoxy network. Thermal characterization shows that methacryloxy-cured systems are more resistant to mechanical penetration and have higher glass-transition temperatures and better stability with regard to thermal decomposition as compared with the conventional diamine-cured epoxy networks. Dynamic mechanical experiments and stress-strain tests also indicate that Bis-GMA based networks have higher tensile moduli and lower elongation at break. Using different modifiers such as 2-ethylhexyl acrylate, the tensile and impact properties of the networks can be improved.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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