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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 103-114 
    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 crosslinking reaction of an epoxy-based resin has been monitored by observing the time evolution of the thermal diffusivity of the mixture, using photoacoustic spectroscopy. The results are interpreted in terms of the expected thermal properties of liquids, polymers and solids, and a comparison with the reported viscosity behavior in similar systems is also made. The potential of the technique for following the curing process is discussed.
    Additional Material: 8 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 32 (1986), S. 6095-6106 
    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: Blends of poly(ethylene ortho-phthalate) (PEOP), and poly(vinyl acetate) (PVAc), appear to be compatible at all compositions, from visual examination at room temperature and differential scanning calorimetry tests. Both low- (PEOP-1) and high-molecular weight (PEOP-2) alloys with PVAc show a single composition-dependent glass transition temperature (Tg). Some blends show Tg values that are below the Tg for either of the pure polymers. Couchman's equation, with a slight modification, can be used to model Tg behavior. All PEOP-2 blends with PVAc, phase separate at high temperatures, whereas PEOP-1-PVAc blends remain miscible under the same conditions. The composition dependence of the blends refractive index shows a deviation from simple additivity rules, and a similar trend is observed in density measurements. When comparing Flory's characteristic parameters for the polymers, compatibility is predicted for PVAc-PEOP blends. In contrast, blends of PEOP and poly(methyl methacrylate) (PMMA), which has a similar chemical structure to that of PVAc are predicted to be incompatible, in agreement with experimental evidence. It is suggested that compatibility is produced because of possible specific interactions between the aromatic group of PEOP and the ester carbonyl on PVAc, which is not sterically hindered as is the corresponding moiety on PMMA.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 39 (1990), S. 1361-1373 
    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 simple method for the iodine doping of atactic polystyrene films is described. The marked changes in the physical properties of the polystyrene films, such as dielectric constant, optical absorption coefficient, and thermal diffusivity, are presented as a function of the doping time. The results show strong evidences of the onset of an order-disorder transition as a function of the doping time.
    Additional Material: 10 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 633-644 
    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: Recently lignin has been the object of a renewed interest because of the need to use raw materials from renewable resources. One such resource is coconut husk, a material usually discarded during the copra extraction process. Due to its high lignin content, coconut husk has been recognized as having a variety of applications. Therefore, it is important to know the approximate structure of coconut husk lignin and those variations introduced by different isolation methods. This work reports a general characterization of coconut husk lignin. Results are given of the contents of hydroxyl and noncondensed guaiacyl units, the extractability of the lignin in alkaline and “organosolv” media along with thermal properties of the extracted lignins. The extraction system of NaOH-anthraquinone at 150°C was most conveniently based on the relatively low amount of condensed lignin generated.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 645-653 
    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: Results of the characterization of coconut husk lignin by infrared (IR) and proton nuclear magnetic resonance (H-NMR) spectroscopy are presented. Lignin was extracted with both alkaline and organosolv liquors. The IR spectra of dioxane lignin were very similar to those reported for hardwood lignins. Furthermore, these results combined with those obtained from the H-NMR studies suggest that coconut husk lignin can be classified into the Lm-type lignins. These lignins are characteristic of the monocotyledon class, of which the coconut palm is a member. The H-NMR studies showed that anthraquinone significantly inhibited the occurrence of lignin condensation during the alkaline extraction with sodium hydroxide solutions. This inhibition was more intense in the lignin extracted at 150°C than in that extracted at 100°C.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 37-44 
    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: In this article we report results of the evaluation of the reactivity of polyphenolic extracts of coconut husk with formaldehyde in both acidic and alkaline media. The objective of this evaluation was to determine if the extracts could be used in the preparation of phenol-formaldehyde-type resins. Extracts were obtained using aqueous solutions of NaOH (with and without anthraquinone) and NH4OH. Because of their low Stiasny's Number values, these extracts are not suitable for phenol-formaldehyde resin preparation in acidic conditions unless they are mixed with phenol or phenolic derivatives. Nevertheless, extracts obtained with NaOH, especially at 100 and 120°C, showed sufficient reactivity with form-aldehyde in basic conditions and may therefore be considered suitable for resin preparation in an alkaline medium. The resins were characterized using infrared spectroscopy (IR), differential scanning calorimetry (DSC), and thermal gravimetric analysis (TGA). A transition temperature prior to decomposition was not detected; their thermal stability was similar to phenol-formaldehyde-type resins. © 1993 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
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  • 7
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Hydrosilylation reactions of 1-allyloxy-3-phenoxy-2-propanol (3) as model compound were carried out with α-dimethylsilyl-ω-hydrooligosiloxane (7; M̄n = 1200) in the presence of hexachloroplatinic acid. It was found that under stoichiometric conditions only 75--80% of the allyl groups were hydrosilylated, due to some isomerization of the allyl groups into vinyl groups, which do not undergo hydrosilylation. This isomerization could be shown to be sensitive to the type of the allyloxy structure. Thus, for example, allyloxybenzene does not undergo isomerization.
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1691-1703 
    ISSN: 0887-624X
    Keywords: 3-alkoxy-5,7-diiodo-6-fluorones ; visible photoinitiators ; acrylate photopolymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several 3-alkoxy-5, 7-diiodo-6-fluorones (λmax ≈ 470 nm) have been synthesized and evaluated as initiators for photopolymerization triggered with the 515.5 nm line of an Ar+ laser. 2-Acyl- and 2-alkyl-4,5,7-triiodo-3-hydroxy-6-fluorones were also tested at 515.5 nm. 9-Cyano-2-Acyl- and 9-cyano-2-alkyl-4,5,7-triiodo-3-hydroxy-6-fluorones were studied and could be excited with the 632 nm line of a He-Ne laser. Dyes with long linear carbon chain alkoxy groups at C-6 showed larger molar extinction coefficients and formed polymers with better mechanical properties than did compounds with shorter carbon chains, or did the corresponding C-6 phenols. The optimum side chain length of the C-6 ether alkyl group is between 4-7 carbon atoms. With longer carbon chain alkoxy groups at C-8, e.g., octyl, the mechanical properties of the formed polymers are inferior to systems formed with the butyl isomer as photoinitiator. In the case of alkoxy groups with branched alkyl groups (e.g., 2-ethylbutyl), the relationship between dye structure and the properties of the polymers formed is less straightforward. Though the dyes react from their triplet state, the fluorescence quantum yields of the dyes and the performance of the dyes as photoinitiators appear directly related. © 1995 John Wiley & Sons, Inc.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1579-1592 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Differential scanning calorimetry (DSC) has been utilized in several studies on polymerization kinetics, at different heating rates. However, there are several factors affecting the precision of kinetic parameters. In this work, the activation energy of urethane-bond formation between 2,6-tolylene diisocyanate and diethylene glycol is reported, the latter being in excess in order to minimize problems such as thermal transitions and incomplete reaction in the final step. The DSC technique was applied at different heating rates. Both the equal conversion and equal conversion rate options of the method are discussed. The latter appears to be a more adequate option for the system studied here. The results obtained show a good agreement with the model used.
    Additional Material: 8 Ill.
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  • 10
    ISSN: 0935-9648
    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
    Additional Material: 1 Ill.
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