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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 57 (1986), S. 1182-1184 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: A dual chamber capillary viscometer (DCCV) has been designed and constructed to measure steady shear viscosity of concentrated polymer solutions at temperatures above the solution normal boiling point. Projected equipment capabilities are as follows: Shear rate: 102≤γ(overdot)≤104 s−1, Viscosity: 10−1≤η≤104 Pa s, Temperature: 300 ≤T≤520 K. Equipment design and results using Newtonian viscosity standards and various Newtonian polymer solutions are presented. Viscosity results determined with Newtonian standards are within ±5% or better of the reported values and two different concentrated polymer solutions and a paper coating (a suspension of clay in a starch-water solution) were used to test the equipment capabilities over wide ranges of shear rate, viscosity, and temperature. The ranges of equipment capabilities tested to date are Shear rate: 300≤γ≤5500 s−1, Viscosity: 0.12≤η≤7.5 Pa s, Temperature: 299≤T≤399 K.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 33 (1994), S. 428-435 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 34 (1995), S. 382-391 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial and engineering chemistry 24 (1985), S. 608-614 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 40 (1994), S. 187-192 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 158 (1972), S. 27-37 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Zur Untersuchung der Kinetik der radikalischen Polymerisation des Acrylamids bei Monomerkonzentrationen unter 0,1 m wurde ein spezielles Dilatometer konstruiert. Die Initiierung der Polymerisation erfolgte durch 4.4′-Azo-bis-4-cyanovaleriansäure in wäßriger Lösung bei 25°C.Aus den m't einem Testversuch der Anfangskonzentrationen [M] = 0,093 m und [I] = 2,09·10-3 m bestimmten Ausdehnungs- und Viskositätsdaten konnte ein fkd-Wert von 2,81·10-8 sec-1 berechnet werden. Ein Vergleich mit extrapolierten Literaturangaben für kd bei 25°C ergab einen Wirkungsgrad f von 0,65 Die fkd- und f-Werte in dieser Untersuchung sind vergleichbar mit anderen veröffentlichten Angaben.Die gefundene Polymerisationsgeschwindigkeit von der Ordnung 3/2 in bezug auf die Konzentration [M] zeigt, daß die Ordnung für Monomerkonzentrationen unter 0,1 m größere Werte als 1 annimmt. Die Ergebnisse können im Rahmen der Käfig-Effekt-Theorie erklärt werden.
    Notes: A dilatometer was constructed to study the free radical polymerization kinetics of acrylamide below 0.1 M monomer. The polymerization was initiated by 4.4′-azo-bis-4-cyano-pentanoic acid in aqueous solution at 25°C.The fkd value, calculated from dilatometric and viscometric data for a test with initial concentration [M] = 0.093 M and [I] = 2.09·10-3 M, was 2.81·10-8 sec-1. Comparison with an extrapolated literature value for kd at 25°C indicated an efficiency value, f, equal to 0.65. Both fkd and f were comparable in magnitude to results of other cited investigations.The results of a 3/2 order dependency of polymerization rate on [M] substantiated the apparent tendency of acrylamide concentration exponents to increase above 1.0 below 0.1 M monomer. A cage effect theory was offered as an explanation for this phenomenon.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 50 (1993), S. 1131-1140 
    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 optical effects (fluorescence, anisotropy, and absorption) of kraft lignin solutions in three different kinds of solvents (0.1N NaOH, DMF, and pyridine) on the measurement of the weight-averaged molecular weight of lignin were investigated, and a correction procedure for these optical effects in the determination of the weight-averaged molecular weight of kraft lignin was developed. It was found that the fluorescence effect is the main source of error in the determination of the molecular weight of lignin, and the anisotropy and absorption strongly affect the second virial coefficient. It was also found that the anisotropic effect of kraft lignin dissolved in DMF and pyridine is contributed mainly by the anisotropic solvents rather than by the lignin particles and that the lignin solution in 0.1N NaOH is essentially optically isotropic. By using the correction procedure provided, the corrected molecular weight of lignin determined in three kinds of solvents varies only about ±10%, whereas the apparent weight-averaged molecular weight of the same lignin differs by ±57%. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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