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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 8 (1962), S. 681-685 
    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: 4 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 8 (1962), S. 365-368 
    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: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 40 (1994), S. 1193-1202 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Sol-gel techniques have shown great potential for producing ceramic materials of designed composition and properties. A typical sol-gel process involves the hydrolysis and polymerization of one or more metal alkoxides in an alcohol solution in a batch reactor to form a homogeneous gel, which is then further treated to provide the type of ceramic desired (such as aerogel, glass, crystal, and coating). Several authors have suggested that diffusion effects may influence the development of the gel microstructure. We investigate what governs the diffusivity of the precursors using the pulsed-gradient-spin-echo NMR technique. This initial report focuses on the early stages of the batch reaction.The system chosen is the acid catalyzed hydrolysis and condensation of tetraethyl orthosilicated in ethanol. 1H PGSE NMR and 29Si NMR show that the diffusivities of the silicate precursors are strong functions both of the molecular weight and of hydrogen bonding between the polar functional groups and the solvent. Moreover, since hydrolysis increases and polymerization reduces the concentration of these polar groups, the mobility of the reactive oligomers changes in a complex manner. Combining our results from PGSE NMR and gas chromatography, we estimate the extent of hydrogen bonding effect on the mobility of various oligomers, providing a model to predict diffusivity trends throughout the batch reaction.
    Additional Material: 10 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 1 (1955), S. 335-341 
    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: 12 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 1 (1955), S. 125-128 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The characteristics of five Herschel-type Venturi tubes with throat diameters ranging from 0.073 to 0.359 in, and throat-to-pipe - diameter ratios from 0.0882 to 0.4340 have been investigated.
    Additional Material: 9 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 40 (1994), S. 925-934 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A new adsorption model is developed for small molecules in zeolites whose form is based on features revealed by molecular simulation. Adsorption is assumed to occur onto a 3-D polyhedral lattice, and both the energy and entropy of the lattice sites are accounted for using a statistical mechanics approach. Energetic interactions are described by an Ising model with both 2- and multibody nearest-neighbor in-teractions. Entropic interactions are included by an adsorption site volume term which accounts for the loss of traslational freedom associated with lattice crowding.The model is applied to a system of small molecules (xenon, methane) adsorbed in idealized zeolite NaA, where adsorption has been shown by computer simulation to occur on finite, cuboctahedral lattices (Van Tassel et al., 1992). The model quantitavely predicts the simulated isotherm over the entire pressure range. Comparison is made with a Langmuir model and a van der Waals gas model which, although valid at low pressures, fail at high pressures due to overestimation of translational entropy and inaccurate portrayal of sorbate-sorbate interaction energy.
    Additional Material: 16 Ill.
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  • 7
    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: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 144 (1986), S. 73-86 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Copolymerisation von Acrylamid (AM) mit N-(1,1-Dimethyl-3-oxobutyl)-N-(n-propyl)acrylamid (PDAAM) wurde im Bereich von 5 bis 20% PDAAM in der Ausgangsmischung untersucht. Die Copolymerenzusammensetzungen wurden mit Hilfe der Elementaranalyse und der 13C-NMR-Spektroskopie ermittelt. Untersuchungen des Reaktivitätsverhältnisses wurden durchgeführt und der Wert des Produktes r1 r2 zu 2,20 bestimmt. Die Molekulargewichte der Copolymeren sinken mit steigendem PDAAM-Gehalt in der Ausgangsmischung. Die Mikrostruktur der Copolymeren wurde aus den experimentell bestimmten Reaktivitätsverhältnissen ermittelt. Diese Modellstrukturen wurden zur Abschätzung der Beziehung zwischen Struktur und Eigenschaften in verdünnter Lösung verwendet, die in einer nachfolgenden Veröffentlichung vorgestellt wird.
    Notes: The copolymerization of acrylamide (AM) with N-(1,1-dimethyl-3-oxobutyl)-N-(n-propyl)acrylamide (PDAAM) has been studied in the range from 5 to 20% PDAAM in the feed. The copolymer compositions have been determined from elemental analysis and 13C-NMR. Reactivity ratio studies have been performed and the value of r1 r2 determined to be 2.20. The molecular weights of the copolymers were found to decrease with increasing PDAAM content in the feed. The copolymer microstructures were predicted from the experimentally determined reactivity ratios. These model structures are utilized for assessment of structure/dilute solution property relationships reported in a subsequent paper in this series.
    Additional Material: 2 Ill.
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  • 9
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Lösungseigenschaften von Copolymeren aus Acrylamid (AM) und N-(1,1-Dimethyl-3-oxobutyl)-N-(n-propyl)acrylamid (PDAAM) mit bekanntem Molekulargewicht wurden in Abhängigkeit von der Zusammensetzung, von zugesetzten Elektrolyten und der Polymerkonzentration untersucht. Arrhenius-Untersuchungen wurden mit Hilfe der Viskosimetrie und der NMR-Spektroskopie durchgeführt. Untersuchungen der Phasenseparation wurden mit Hilfe von Trübungstitrationen vorgenommen. Die Lösungseigenschaften der AM-PDAAM-Copolymeren werden durch die Anwesenheit von intramolekularen hydrophoben Wechselwirkungen bestimmt. Diese Wechselwirkungen können zu einer Abnahme der hydrodynamischen Ausdehnungen im Vergleich zu Polyacrylamid mit ähnlichem Molekulargewicht führen.
    Notes: Solution properties of copolymers of acrylamide (AM) with N-(1,1-dimethyl-3-oxobutyl)-N-(n-propyl)acrylamide (PDAAM) of known molecular weight have been studied as a function of composition, added electrolytes, and polymer concentration. Arrhenius-type studies have been performed by viscometry and NMR to assess the effects of temperature. Phase separation studies have also been performed using turbidimetry. The solution properties of the AM-PDAAM copolymers are dictated by the presence of intramolecular hydrophobic interactions. These interactions may result in decreased hydrodynamic dimensions relative to polyacrylamide of similar molecular weight.
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 36 (1959), S. 341-349 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Analysis of sedimentation velocity experiments employing a θ solvent has been applied to measure the molecular weight distribution of both broad- and narrow-distribution polystyrene. The θ solvent was found necessary for satisfactory results. The required sedimentation constant-molecular weight relationship was obtained from both intrinsic viscosity data and molecular weights obtained by Archibald's method.
    Additional Material: 6 Ill.
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