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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 191 (1961), S. 1292-1293 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Table 1. VALUES OF (Q - Qo) AND (A -Ao) FOR 1 PER CENT SOLUTIONS OF POLYMERS 1 (Q-Qo) (A-Ao) Polymer Mn Solvent (k.cal.) (x 106) acetone 0-3 2-6 Poly vinyl acetate 148,000 chloroform 0-3 0*2 9-6 Polymethyl meth- acetone -016 11-0 acrylate 121,000 toluene -01 9-6 benzene nil 4-9 ...
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 200 (1963), S. 1095-1096 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Table 1 'Oxidizing Direct bromide Total bromide Tempera- power' content content Treatment ture () (m.equiv. mole-1) (m.mole Br~ mole-1) (m.mole Br-1 mole-1) None 20 17-1 7-2 12-2 Compressed, 1,000 atm. 20 15-9 7;4 12-1 Compressed, 2,000 atm. 20 ...
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of food science 50 (1985), S. 0 
    ISSN: 1750-3841
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: When cake batters prepared with chlorine (Cl2)-treated and untreated flours were heated in the Rheometrics Dynamic Spectrometer (RDS), elasticity G′ increased between 90°C and 100°C for the Cl2-treated sample and not for the untreated sample. Therefore, at 100°C, the batters prepared with Cl2-treated flours had a much higher G′ than the batter prepared from untreated flours. Flour-water systems prepared with Cl2-treated and untreated flours showed no difference in G′. This inferred that there was an interaction with at least one formula ingredient. Defatting both Cl2-treated and untreated flours did not alter the RDS results.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 8 (1969), S. 184-187 
    ISSN: 1435-1528
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Zusammenfassung Die vorliegende Abhandlung befaßt sich mit der Eichung und dem Gebrauch eines Epprecht-Rheomats mit besonderer Hinsicht auf nicht-Newtonische Flüssigkeiten. Ein Verfahren zur exakten Berechnung von Scherwerten für nicht-Newtonische Flüssigkeiten läßt sich aus derEuler-Maclaurinschen Summenformel ableiten. Einige Beispiele zur Berechnung von Scherwerten für Weichmacher von Polyvinylchlorid sind beigefügt.
    Notes: Summary This paper deals with the calibration and use of an Epprecht Rheomat with particular reference to non Newtonian liquids. A method of calculating accurate rates of shear for non-Newtonian flow is derived using theEuler-Maclaurin sum formula. Some examples are given of the calculation of shear of poly vinyl chlorideplasticiser suspensions.
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 206 (1965), S. 184-184 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The use of rate process theory as applied to the flow of high polymer molecules6,7 may provide a clearer picture of the nature of these contributions to DS and a more precise interpretation of the variations of DS with c and M. It is generally accepted that the flow of flexible high polymer chains ...
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 4 (1965), S. 40-47 
    ISSN: 1435-1528
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of electronic testing 6 (1995), S. 153-177 
    ISSN: 1573-0727
    Keywords: testing regular arrays ; test vector generation ; C-testability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Electrical Engineering, Measurement and Control Technology
    Notes: Abstract In recent years the concept of ‘Design for Test’—whereby the designer is forced to comply with a specific test style—has become very popular. However, the most effective custom VLSI architectures available all have their own very strongly defined structure. Therefore, test strategies are required which exploit the typical hierarchy in the design. Exploiting this hierarchy implies a test philosophy which requires the minimum addition of extra test logic and utilizes the hierarchy of the design. A popular VLSI architecture is a systolic array which consists of a regular array of small processing elements with timing latches on the communication lines. In this case we can exploit the regularity for test purposes; in this paper we show how to do this by adopting a divide and conquor method. This can be done by generating test vectors for a single processing element, using the most appropriate fault model. The regularity of the array facilitates the propagation of these vectors to every other processing element in the array. The propagation method must also allow for the propagation of the fault effects from the output of each processing element to the boundary of the array where the fault can be observed. The proposed test method presented in this paper takes the vectors required to test a single processing element, and determines test vectors for the whole array. This method is applicable to all types of regular arrays, but in particular, systolic arrays, where we have the added problem of circuit timing. Each separate signal direction is first analyzed for its test vector and fault effect propagation properties. Then, using the array Data Dependence Graph, which represents the propagation of data through the array, the combined effect of all signals on test vector and fault effect propagation can be considered. This reduces the task of determining the array inputs to a pattern matching problem suitable for computer implementation. The test method is applied to three different arrays to illustrate how different array types can be tested.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 10 (1966), S. 1121-1132 
    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: Reduced melting point and swelling measurements, involving heptane-soluble material from atactic polypropylene and over thirty liquids of differing chemical type, are reported. A value of 578 ± 40 cal. is obtained for the molar heat of fusion of a crystalline repeat unit which is much lower than values given for isotactic polypropylene. Some reasons for the low value are considered. Values of the polymer-solvent interaction parameter χ1 for systems involving alkylbenzenes and n-alkanes suggest a solubility parameter of 7.9 ± 0.1 (cal./cc)1/2 for the polymer. These values of χ1 decrease with increasing molar volume of liquid. Polar liquids of comparable solubility parameter or molar volume are associated with higher values of χ1. Intrinsic viscosities and values of the slope constant k′ are given for fractions in the molecular weight range 3,000-25,000 and six solvents at 25°C. The results suggest the following order of solvent power: cyclohexane ≈ cyclohexene 〉 methylcyclohexane 〉 trichloroethylene 〉 decalin 〉 carbon tetrachloride. Intrinsic viscosities are higher than those generally obtained for flexible polymers of comparable molecular weight, and the values of the Mark-Houwink exponent appear to be high. Some reasons for these high values are considered.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 2619-2630 
    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: Osmotic, viscometric, and initial phase separation studies of dilute solutions of poly-(vinyl chloride) in cyclohexanone, cyclopentanone, tetrahydrofuran, morpholine, nitrobenzene, and tetrahydropyran are reported together with some swelling measurements involving these solvents and dioxane, acetone, and methanol. Values of the polymer-solvent interaction parameter χ1 obtained from osmotic and swelling measurements suggest the order of solvent power for poly(vinyl chloride) to be cyclohexanone 〉 cyclopentanone 〉 tetrahydrofuran 〉 morpholine 〉 nitrobenzene 〉 tetrahydropyran. A similar order is suggested by the volumes of hexane required to cause initial phase separation. Values of intrinsic viscosity and of the viscosity slope constant k′ give somewhat different orders of solvent power. Reasons for differences in order are considered. The correlation of the volume of hexane required to cause initial phase separation with χ1 is discussed and it is suggested that the polymer is solvated in solution. Other factors affecting the solvent power of solvents for poly(vinyl chloride) would appear to include the bulk and the solubility parameter of the solvent.
    Additional Material: 3 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 2019-2029 
    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 sample of commercial atactic polypropylene was extracted with ether and the residue extracted with boiling n-heptane. Six fractions of the heptane-soluble material, which is very similar to that obtained by heptane extraction of isotactic polypropylene, were obtained by stepwise addition of acetone to a solution in cyclohexane. Densities, melting points, and x-ray photographs of the fractions and the unfractionated material were obtained and infrared absorption spectra used to estimate tacticity. Molecular weights, determined by means of a vapor pressure osmometer, ranged from about 3000 to about 25,000. That of the fraction of highest molecular weight was in good agreement with a separate determination by means of osmotic pressure measurements. Separation in fractionation occurred in order of decreasing molecular weight and increasing crystallinity as estimated from densities and x-ray photographs. Tacticity also seems to increase with decreasing molecular weight. Melting points of the fractions were not entirely in the order expected from their molecular weights and estimated crystallinities, and it is possible that low DP isotactic material may be preferentially concentrated in the highest molecular weight fraction. It is emphasized that the unfractionated material may contain polymers possessing a range of order intermediate between those of purely atactic and purely isotactic polymer and that refractionation may be required in order to characterize the material completely.
    Additional Material: 5 Ill.
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