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  • Polymer and Materials Science  (12)
  • 2005-2009
  • 1980-1984  (8)
  • 1955-1959  (4)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 1681-1688 
    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 use of a new class of thermoset organotin epoxy polymers as matrix resin for composites has been evaluated. Copolymers of maleic anhydride with hexene-1, decene-1, or styrene were partially esterified with tributyltin, and the residual carboxyl groups were crosslinked with glycidyl methacrylate when preparing glass fabric-reinforced composites. Glass composites were also prepared from DGEBA cured by tributyltin 3,5-diaminobenzoate. The tensile, flexural, and impact strengths of the composite specimens warrant their use in structural applications requiring antifouling protection.
    Additional Material: 4 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 2093-2103 
    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 critical element for a durable exterior clear coating on wood is photochemical stability of the wood surface beneath the coating. If this interface is not stabilized, even a durable coating will delaminate due to photoinduced wood degradation. A new method for stabilizing the wood surface was developed and evaluated. HEBP [2-hydroxy-4-(2,3-epoxypropoxy)benzophenone] was grafted to western redcedar (Thuja plicata). HEBP contains an ultraviolet (UV) stabilizer moiety that improved the xenon are accelerated weathering performance of western redcedar (WRC). The weathering performance of the HEBP-modified WRC was compared with WRC treated with an unbound UV stabilizer of similar type and with untreated controls. The grafted stabilizer reduced the erosion rate (weathering) of unfinished WRC, and, as a pretreatment under clear finishes (spar varnish and exterior grade polyurethane), the stabilized surfaces improved coating performance and color retention.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 383-397 
    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: A method has been developed to quantitatively measure the surface plasticizer levels present on test plaques made from a plasticized PVC compound. The plaque fabrication conditions have been chosen so that the plaque closely models an extruded flexible PVC profile. The analysis method utilized sorption of the surface plasticizer on fumed silica, followed by methanol extraction and liquid chromatographic identification and quantitation of the plasticizer. Typical results are presented for a model compound plasticized with either di-2-ethylhexyl phthalate (DOP) or a mixture containing predominantly linear C7, C9, and C11 dialkyl phthalates (DHNUP). The effect of compound work level, as measured by Banbury drop temperature and final processing temperature, has also been studied. These results show that, for the model compound studied, the average surface level of DHNUP is always greater than that of DOP. The DOP levels are essentially independent of compound work level. The DHNUP levels generally increase with increasing mold temperatures. Finally, this data has been correlated with a study of the lifetime of a Neoprene-based adhesive bond to DOP-and DHNUP-plasticized flexible PVC in a 100°C oven. These studies clearly show that a one-to-one substitution of DOP for DHNUP will increase the time to adhesive bond failure by a factor of at least 10 with this particular adhesive system and model compound.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 2481-2492 
    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 curing reaction of a commercial bisphenol A diglycidyl ether (BADGE) with ethylenediamine (EDA) was studied by differential scanning calorimetry. Different kinetic expressions were found with isothermal (low temperature range) and dynamic (high temperature range) runs. Two competitive mechanisms are shown to be present: an autocatalytic one (activation energy E = 14 kcal/mol) and a noncatalytic path characterized by a second-order reaction with E = 24.5 kcal/mol. At low temperatures both mechanisms took place simultaneously, showing a significant decrease in the reaction rate after the gel point. At high temperatures only the noncatalytic reaction was present, without showing a noticeable rate decrease in the rubber region. Also, a third-order dependence of the glass transition temperature on reaction extent is shown.
    Additional Material: 8 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 893-901 
    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 curing of novolacs with paraformaldehyde is analyzed with several experimental techniques (DSC, IR, sol fraction) as well as statistical arguments. Results for typical novolacs show that a maximum crosslinking density is attained at a mass ratio mP/mN close to 0.20. However, at mP/mN greater than 0.10, hemiformals appear in the cured product, increasing the amount of extractable formaldehyde. The heat of reaction increases linearly from mP/mN = 0 to 0.15, attaining a maximum value of -ΔH = 98 cal/g novolac at mP/mN ∼ 0.20. The curing kinetics follows an overall second-order law with an activation energy E = 32.5 kcal/mol and a preexponential factor A = 1.1 × 1015 min-1 (both for mP/mN 〉 0.1).
    Additional Material: 5 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 485-499 
    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 curing kinetics of a general purpose unsaturated polyester (UP) with styrene was studied by differential scanning calorimetry and dielectric capacitance measurements. Benzoyl peroxide was used as initiator. Results showed that there is a complete change in the phenomenological kinetics, in different temperature ranges. At low temperatures (70-90°C), the rate went through a maximum and then showed a first-order decay. At high temperatures (100-160°C) a second-order kinetics was suitable for all the conversion range. At T 〉 160°C another mechanism took place when the initiator amount was less than a critical value. From the changes in the dielectric capacitance it was inferred that the conversion rate of UP unsaturations followed a first-order decay after a certain conversion, with an activation energy close to values reported for diffusion of UP radicals. Possible free radical mechanisms accounting for experimental observations are discussed.
    Additional Material: 12 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 26 (1957), S. 199-212 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The rates of denaturation of arachin and conarachin II with sodium hydroxide and guanidine hydrochloride have been studied. Arachin is more susceptible to denaturation with both reagents. The rates of denaturation of the two proteins with sodium hydroxide or guanidine hydrochloride are decreased by increasing the sodium chloride concentration. Arachin is changed by both denaturants to slowly sedimenting material by way of an intermediate sedimenting component, but no intermediate component has been observed with conarachin II. Whereas the rate of alkaline denaturation of both proteins is very sensitive to temperature changes, with guanidine hydrochloride the rate is not affected appreciably by changes in temperature. This would indicate that an appreciable activation energy is required for the alkaline denaturation. Confirmation of this is seen in that the alkaline denaturation is always completely irreversible whereas with guanidine hydrochloride some reversibility has been observed. Although there was no increase in rate with increase in protein concentration for either protein, in no case did the plot of log concentration vs. time give the straight line graph expected of a reaction which is first order with respect to protein concentration.
    Additional Material: 7 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 32 (1958), S. 193-206 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The denaturation of arachin and conarachin II with urea, guanidinium chloride and thiocyanate, and of arachin with alkali metal thiocyanates and lithium halides has been examined using sedimentation velocity and viscosity techniques. The effect of various anions on the alkaline denaturation of arachin has also been investigated. It was found that with reagents which denature arachin and conarachin II at similar rates, the arachin half molecule was not observed as an intermediate stage in the arachin denaturation with the exception of lithium chloride. The denaturation of arachin with urea and guanidinium chloride was faster at pH 10 than at pH 8. The denaturing power of the alkali metal thiocyanates decreased in the order Li, Na, K, and of lithium halides in the order Lil, LiBr, LiCl. It was found that in the case of denaturation with guanidiniun and alkali metal salts, the cation appeared to be the main denaturant but anions inhibited the denaturation with the exception of the thiocyanate ion which was either noninhibiting or was itself a denaturant. With ionic denaturants in general the nature of both ions was important.
    Additional Material: 9 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 31 (1958), S. 35-44 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dissociation of arachin has been studied over a range of pH values, ionic strengths, temperatures, and protein concentrations and standard energy values have been calculated. The standard entropy changes and standard heat contents were found to be lower than would be expected and possible reasons for this are discussed. The Kc values varied on altering the protein concentration and are considered to be dependent on a function of the ratio of concentration to ionic strength.
    Additional Material: 3 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 35 (1959), S. 465-473 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of a number of electrolytes on the denaturation of arachin with urea and guanidinium chloride has been examined by ultracentrifuge and viscosity techniques. With urea, all the sodium salts studied retarded the denaturation. With guanidinium chloride, however, it appeared that a salt accelerated or retarded the denaturation depending upon whether the guanidinium salt with the anion of the salt in question denatured arachin more rapidly or more slowly than guanidinium. chloride. The effect of some other guanidinium salts on the sedimentation of arachin is also briefly reported.
    Additional Material: 8 Ill.
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