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  • Wiley-Blackwell  (29)
  • Oxford University Press  (4)
  • American Institute of Physics (AIP)
  • American Chemical Society (ACS)
  • 1965-1969  (23)
  • 1955-1959  (10)
  • 1
    Electronic Resource
    Electronic Resource
    The evaporation of carbon tetrachloride in a wetted-wall column (1965)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 11 (1965), S. 1139-1142 
    Details
    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: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690110633
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  • 2
    Electronic Resource
    Electronic Resource
    Promotion of drop-by-drop condensation of steam from seawater on a vertical copper tube (1968)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 14 (1968), S. 245-250 
    Details
    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 limited number of tests were made of promoters, their method of application, corrosion resistance, etc.The best promoter found to date is tetrakis octadecyl thio silane (C18H37S)4Si which differs only in parafinic chain length from (C12H25S)4Si which was found to be one of the best promoters for drop-by-drop condensation by Blackman and Dewar (1, 2), Hampson (2, 3), and Osment (4, 5). These compounds are nontoxic.The C18 compound appears to be superior to the C12 compound in that it is less volatile, lower melting (∼34°C), and appears to impart superior oxidation resistance to copper when adsorbed on clean oxide-free metal.Copper tubes can be rapidly cleaned in place by sulfur dioxide or hydrochloric acid in steam, or, if previously promoted by a thio silane, by treatment first with chlorine gas in steam.The thio silanes may be rapidly applied as a 1% solution in octanoic acid injected into the sea-water feed. The acid acts as cleaner and poor promoter, allowing the good promoter molecules to contact the metal tube.The amounts of the best promoters required are in the parts per billion range.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690140209
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  • 3
    Electronic Resource
    Electronic Resource
    Water-oil displacements from porous media utilizing transient adhesion-tension alterations (1965)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 11 (1965), S. 617-624 
    Details
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Previous laboratory studies have demonstrated that the injection of small quantities of reverse-wetting agents during water displacement can increase oil recovery from unconsolidated porous media. Hexylamine is a suitable reverse-wetting agent. It has been found that the effectiveness of this treatment increases with the quantity of amine injected (slug volume and/or amine concentration in the slug), and that treatments sufficient to stimulate oil production at high water flow rates did not do so at low flow rates. It has been established that the stimulation of oil production by this technique is accomplished by transient adhesion-tension alterations, resulting in the spontaneous accumulation of oil into large continuous masses which are subsequently mobilized.The present investigation has attempted to investigate the effect of other variables thought to be important in this system in order to clarify the mechanism by which increased oil recovery is effected. Specifically, the mechanism by which large oil masses are formed and propagated was studied.Displacement studies conducted in a glass-grid micromodel, under cinemicrographic observation, revealed that large oil masses form as a consequence of restoration of water wettability (amine desorption) but only if the local oil saturation exceeds the irreducible minimum value (under water-wet conditions). Mobilization of these oil masses was observed under the influence of a favorable wettability gradient.Displacement studies were also performed in unconsolidated silica sand beds, under conditions of varying oil-water viscosity ratio, hydraulic permeability, flow rate, and time at which the amine was injected. In the range of the variables investigated, the additional oil recovered (by treatment) increased as the viscosity ratio increased oil recovery. Water-oil displacement efficiencies enhanced by amine treatment were found to correlate satisfactorily with a parameter representing the ratio of the hydraulic forces to the capillary forces within the medium.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690110412
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  • 4
    Electronic Resource
    Electronic Resource
    Direct contact heat transfer between immiscible liquids in turbulent pipe flow (1968)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 14 (1968), S. 151-158 
    Details
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: This paper reports on an experimental study of the direct contact heat transfer between oil and water in turbulent pipe flow under nonboiling conditions. Data were taken by a new technique, namely, monitoring on a very fast response recorder the output of a small thermocouple placed in the two-phase flow. The variables studied were the liquid velocity, the pipe diameter, the water volume fraction, and, to a lesser degree, the interfacial tension and the oil viscosity. A successful semiempirical method of correlating the data is also presented.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690140126
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  • 5
    Electronic Resource
    Electronic Resource
    Interfacial polymerization of n-alkyl α-cyanoacrylate homologs (1966)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 10 (1966), S. 1617-1623 
    Details
    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 n-alkyl α-cyanoacrylates from methyl through n-octyl exhibit a reverse order of polymerization rate on biological substrates compared to that on water. On water, the lower homologs spread and polymerize rapidly, whereas the higher homologs spread but polymerize slowly. On biological substrates, the lower homologs do not spread or spread slightly and the higher homologs exhibit large spreadabilities and very rapid polymerization rates. Determination of the spreading coefficients for these systems by using the monomers or model compounds confirm the observed spreadabilities. It is proposed that the increased rate of polymerization of the higher homologs on biological substrates may be due to increased catalyst concentrations on these surfaces or to the solubilization of the higher homologs at the interface, making the catalyst sites more available to the monomer. The suggestion is made that if the liquid monomers spread and orient on the substrate and subsequently polymerize, the polymers will maintain the orientation. If such is the case, a technique is available for preparing stereospecific vinyl polymers which may have different spatial configurations depending on the polarity of the liquid substrate upon which they have been allowed to spread and polymerize.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1966.070101101
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  • 6
    Electronic Resource
    Electronic Resource
    Polymer degradation. V. Changes in molecular weight distributions during sonic irradiation of polyisobuteneProd. No. 1470 (1967)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 335-340 
    Details
    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: Gel permeation chromatography was used to follow changes in the molecular weight distribution of a polyisobutene, initial Mv = 466,000, during degradation induced by sonic irradiation. Seven samples taken at times of 200-163,500 sec. were studied. In general, a steady decrease in molecular weight was observed, although a bimodal distribution was present after 20,000 sec. irradiation. Various measures of inhomogeneity, Mw/Mn, U, etc., were examined. The function, σn/Mw, where σn is the standard deviation of the number distribution, is considered as a measure of the relative distribution. It is shown to be almost constant throughout the degradation.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1967.070110302
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  • 7
    Electronic Resource
    Electronic Resource
    Characterization of block and random ethylene-propylene copolymers by differential thermal analysisPresented in part before the Division of Polymer Chemistry, 148th National Meeting of the American Chemical Society, Chicago, August 30-September 4, 1964. (1965)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 3061-3069 
    Details
    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 group of C14-tagged ethylene and propylene polymers consisting of physical mixtures of homopolymers, block copolymers made up of two homopolymer sequences, and block copolymers made up of several homopolymer segments has been studied by differential thermal analysis (DTA). The effect of randomness in copolymers has also been studied in this set of systems, which contains 0-51 wt.-% ethylene. Block copolymers and physical mixtures have been found to have thermograms with endothermal minima at approximately 138 and 163°C. The ratio of heights of the two minima has been found to be a function of the ethylene and propylene content for mixtures of homopolymers and for block copolymers without randomness. DTA thus provides an analysis for monomer ratios in physical mixtures and in block copolymers of ethylene and propylene. The cooling thermograms of block copolymers have been demonstrated to have two exotherms in all cases where the block ethylene content exceeded 10%; the propylene limit was not fixed. Mixed homopolymers do not exhibit two freezing exotherms. The total heat of fusion of the polymer has been found to be a usable measure of chain randomness and block nature. The conditions for observation of single and multiple transitions have been extended.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1965.070090912
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  • 8
    Electronic Resource
    Electronic Resource
    The nitrosation of nylon (1958)
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 33 (1958), S. 447-455 
    Details
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The nitrosation of nylon 66, with the use of four different nitrosating agents, has been investigated. By the more vigorous nitrosating reactions, heterogeneous nitrosation of nylon yarn occurs rapidly and proceeds to completion in a few hours. In this reaction the amide hydrogen is substituted by a nitroso group to give the structure By heating the nitrosated polyamides, nitrogen is evolved, and polyesters are formed. The kinetics of this change have been fully investigated. Caustic alkali reacts rapidly with nitrosated nylon. Free radicals are produced on exposure of the nitrosated nylon to visible radiation. Partial nitrosation of nylon yarns has been carried out with the use of a running threadline system; the physical properties of the resulting yarns have been examined.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1958.1203312641
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  • 9
    Electronic Resource
    Electronic Resource
    Das Kondensationsprinzip der Catechin-Gerbstoffe (1957)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 90 (1957), S. 957-962 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Kondensation, welche Catechine unter der Einwirkung von Säuren erleiden, besteht in der Substitution einer reaktionsfähigen CH-Gruppe des einen -Moleküls durch das Kohlenstoffatom 2 (Phenylcarbinoläthergruppe) des anderen. Dieses Ergebnis wird an vereinfachten Modellen aus der Gruppe der Catechine abgeleitet.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19570900615
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  • 10
    Electronic Resource
    Electronic Resource
    Synthese des 3-Galloyl-Catechin-AcetatsHerrn Adolf Windaus in alter Verbundenheit gewidmet (1957)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 603 (1957), S. 177-182 
    Details
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tee enthält Gallussäure-ester von Catechinen, in denen die Gallussäure mit dem sek. Carbinol in 3-Stellung verbunden ist. Hier wird die Synthese des 3-Galloyl-d-catechin-heptaacetats (VIII) sowie die Darstellung einiger weiterer d-Catechin-Derivate beschrieben.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jlac.19576030119
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