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  • 1
    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: Polyspiroacetal polymers and copolymers derived from pentaerythritol, and glutaraldehyde were prepared and examined for physical properties. Elemental and infrared analyses support the polyspiroacetal structure. X-ray analysis indicates a range of 20-40% crystallinity. Dipentaerythritol was observed to influence in varying degrees the crystallinity, the solubility, and the optimum range of film curing conditions. Resins with more than 25% dipentaerythritol always crosslinked during polymerization. In addition, the variables influencing such resin properties as molecular weight and gelation were examined. Films crosslinked with pyromellitic dianhydride exhibited good flexibility and tensile strength. Moreover, their oxidative thermal stability was only slightly less than that of crosslinked poly(ethylene terephthalate).
    Additional Material: 5 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 2003-2023 
    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: At temperatures far below the heat distortion point, the dissipation factor (and therefore power factor) of epoxy resins is comparably low - in the order of 0.001-0.01. Internally flexibilized, polyester-modified resins may have higher loss tangents, in the order of 0.01-0.10, even at room temperature. At temperatures far above the heat distortion point, anhydride curing agents give lower dissipation factors than do amines or acids. With anhydride cures, the higher molecular weight resins investigated cure faster than the lower molecular weight resins, give lower elevated temperature power factors and loss tangents, and are tougher. With any hardener-epoxy resin system, the optimum elevated temperature power factor, weight loss on aging and heat distortion point will probably depend on a close examination of the optimum hardener/resin ratio.With certain anhydride-cured low molecular weight epoxy resin systems, an increased rate of cure and lower elevated temperature power factor may be obtained by use of a small amount of higher molecular weight (polyhydroxy) epoxy resin. Attempts to compare the effect on power factor of changing the hydroxyl groups to less mobile dipoles by acetylation were unsuccessful, since the resulting acetoxy groups changed the cure mechanisms. However studies with resins of different molecular weights indicated that the effect of hydroxyl content on elevated temperature power factor is subordinate to other effects such as the rigidity of the cured resin system, rate of cure and ionic impurities. Acetylation of hydroxyl-containing epoxy resins may inhibit cure with some curing agents, due to side reactions of the resulting acetoxy group with specific hardeners.
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 6 (1962), S. 503-507 
    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 reaction of various dialdehydes and one diketone with pentaerythritol or pentaerythritol-dipentaerythritol mixtures, has produced a series of thermoplastic, Polyspiroacetal resins. These possess molecular weights up to 10,000, solubility in a limited range of solvents, and high melting points. Some of these, with an optimum amount of crosslinking, have produced transparent, tough, flexible films.
    Additional Material: 1 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 49 (1961), S. 377-383 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method is demonstrated whereby the rheological and spray properties of dilute polymer solutions can be studied by means of a jet extrusion instrument and a capillary flow consistometer. The rheological properties that can be determined at any shear rate of extrusion are the normal (tensile) stress, the elastic shear modulus, the elastic recoverable shear strain, and viscosity. The spray properties of dilute polymer solutions can be qualitatively described in various terms such as knotted rod, knotted ligaments, long ligaments, threaded drops, grouped drops, or combinations thereof. The method has been successfully employed with dibutyl phthalate solutions of high molecular weight polyisobutyl methacrylates ranging in concentration from 0.5 to 2.0% by weight, and also with several linear polystyrenes of different molecular weights at various concentrations.
    Additional Material: 1 Ill.
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  • 5
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It was shown that diethyl vinylphosphonate and diisopropyl vinylphosphonate are polymerized by peroxide initiators to clear, light-yellow, viscous liquid polymers of low molecular weight. It was found that the yield of the isolated polymers varied directly, while the molecular weight varied inversely, with the concentration of the initiator. Infrared spectra of the monomers used and the polymers obtained established that polymerization occurs through the vinyl group. It is postulated that the low molecular weight is due to the result of chain transfer with polymer and/or monomer through the alkoxy groups attached to the phosphorus atom.
    Additional Material: 5 Tab.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 47 (1960), S. 532-533 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 2 (1964), S. 711-730 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An attempt is made here to delineate some of the consequences of the special properties of coacervating soaps when the soaps are used in the emulsion polymerization of styrene. In dilute solutions an essential difference between a coacervating soap and a noncoacervating soap is the critical suppression of the micellar ionization in coacervating systems when relatively small amounts of simple electrolytes are added to the systems. A direct correlation between the polymerization rates and polymer molecular weights with the state of micellar ionization has been demonstrated. The highest polymerization rates and highest polymer molecular weights occur in solutions in which the coacervating soaps show a maximum ionization. In soap solutions in which the micellar ionization is critically suppressed there is evidence of soap desorption from polymer particles, resulting in the generation of an increasing number of particles during the course of the polymerization. Two coacervating systems and two noncoacervating systems were used in this investigation. For the anionic noncoacervating K laurate-KCl system, where the micellarsize remains practically constant with the addition of electrolyte, the following relationship between the polymerization rate and KCl concentration, up to 1M KCI, has been found: R = R0 + B√C. The effects of the charge properties of soap micelles on the course of the polymerization of styrene have been associated with two effects. (a) For highly ionized micellar systems the micelle periphery presents an open structure due to the coulombic repulsion of the charged polar hydrophilic groups of the soap molecules. This open structure facilitates the diffusion of monomer to the loci of polymerization. (b) Where the micellar ionization is suppressed, monomer diffusion to the loci of polymerization is impeded. Extensive suppression of micellar ionization results in micelles of enhanced stability. In the highly stabilized systems when the loci of polymerization are polymer particles there is competition for soap molecules between the adsorption sites on the polymer particle and soap micelles. The influence of soap concentration on the emulsion polymerization for different soaps and electrolyte concentrations has been investigated. For the coacervating Hyamine 1622 soap at zero electrolyte concentration, the rate of polymerization has been found to be proportional to the 0.5 power of the soap concentration. This relationship is not maintained when electrolyte is added to the polymerization system.
    Additional Material: 12 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 2 (1964), S. 3135-3146 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cyclic and linear formals containing a unique polycycloborane named carborane were prepared. The treatment of carborane glycols with formaldehyde or dipropyl formal yielded cyclic formals, linear polyformals, a mixture of linear and cyclic formals or no formal product depending upon the reaction conditions and the particular carborane glycol used. It was demonstrated that two of the carborane diols have a great tendency to form cyclic formals in solution or bulk-type reactions. In the reaction with 1,2-bis-(hydroxymethyl)carborane, the tendency to cyclize is greater than might be expected for a seven-membered ring. This propensity to form cyclic structure has been attributed to the short carbon-carbon bond and the relatively acute external angle of the group attached to the carborane nucleus. The stability of these cyclics has been demonstrated by failure to open the formal cyclics to form linear polymer. Polymer was obtained with bis(2-hydroxyethyl-1-carboranylmethyl) ether, however, neither cyclic nor polymer products were obtained with bis(2-hydroxymethyl-1-carboranylmethyl) ether. The failure to obtain the desired products have been attributed to the steric requirements of the carborane group.
    Additional Material: 5 Ill.
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  • 9
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polyesters containing a unique polycycloborane in the polymer structure have been prepared. The boron hydride moiety, C2B10H10, has been named carborane and approximates in size a sphere with an effective van der Waals radius of 4 A. Polyesters of 2000-3000 molecular weight were prepared by allowing carborane monomers to react with each other or with organic or fluorocarbon diols or diacids. A polyester of approximately 20,000 molecular weight was prepared and it was demonstrated that molecular weight obtainable was a function of monomer ratio and purity. It was demonstrated that polyesterification of adipic acid with a carborane diol was significantly slower than the analogous reaction with 1,4-butanediol. Reactions of carborane diols with carborane diacids were shown to occur with difficulty or not at all. Transesterification of carborane malonates also occurred with difficulty. The inhibitions of carborane materials toward polyesterification was attributed to both steric and polar influences with the former being more significant. The effect of the bulky carborane group in the polyester chain on the properties of the polymer was demonstrated by the preparation of polyadipates from 1,2-bis(hydroxymethyl)carborane, 1,4-butanediol, and 1,4-butynediol. The first product was a liquid which showed no tendency to crystallize. The noncarborane polyesters were crystalline waxes at equivalent chain length. The bulk of the carborane group apparently inhibited close packing and subsequent crystallization. A comparison of the carborane polyadipate and polysuccinate showed that the latter was a hard glass, apparently due to a decrease in chain flexibility.
    Additional Material: 3 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 2 (1964), S. 1159-1163 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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