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  • Wiley-Blackwell  (71)
  • Oxford University Press  (24)
  • American Chemical Society (ACS)
  • 1990-1994  (72)
  • 1965-1969  (23)
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Year
  • 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
    Spray-to-bubbly transition for distillation systems containing two liquid phases (1991)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 37 (1991), S. 597-606 
    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: The tray hydrodynamics were determined for a system containing water and kerosene as immiscible liquids. Plates with hole diameters ranging from 3.18 to 12.70 mm were used in a 44.5-cm2 perspex air-water-kerosene simulator. Experiments were also carried out in a 50-mm-ID column using different depths of oil and water mixtures to study the drop and bubble mechanisms. A spray-to-bubble transition occurred for the two liquid-phase system experiments. The liquid holdup at the transition increased directly with gas velocity and hole diameter, and decreased with increasing free area. At the same hole velocity, the presence of two liquid phases caused the transition to occur at different liquid holdups than for the single pure liquid. Two different modes of coalescence were observed in the small column work. New correlations have been proposed for the liquid holdup at the transition which allow for the presence of two liquid phases.
    Additional Material: 21 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690370413
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  • 3
    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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  • 4
    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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  • 5
    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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  • 6
    Electronic Resource
    Electronic Resource
    An investigation of the physico-chemical basis of foaming in fungal fermentations (1994)
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 44 (1994), S. 801-807 
    Details
    ISSN: 0006-3592
    Keywords: foaming ; fermentations ; biochemical basis ; biosurfactants ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A detailed physico-chemical analysis of two foaming fungal fermentations was carried out to identify that key groups of compounds responsible for foam formation. Fermentations were carried out on a 20-L scale in a stirred aerated tank, over 7 days, using a commercial, defined medium. The organisms investigated were Penicillium herqueii, a hyphomycete, and an unidentified Ingoldian fungus. Samples of broth and, where possible, foam were analyzed to determine which groups of compounds were concentrated into generated foams. Surface tension, bulk viscosity, and antifoam A concentration were additionally determined in broth samples. To date the cause of foaming in fermentations has been attributed to the surfactant properties of extracellular proteins. This assumption was tested and found to be incomplete as many additional groups of biochemicals were found to be enriched into the foam. The results of the investigation revealed the presence of proteins, carbohydrates, α-keto acids, and lipophilic biosurfactants, particularly extracellular pigments, enriched within stable foams. © 1994 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bit.260440705
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  • 7
    Electronic Resource
    Electronic Resource
    Rapid screening for metabolite overproduction in fermentor broths, using pyrolysis mass spectrometry with multivariate calibration and artificial neural networks (1994)
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 44 (1994), S. 1205-1216 
    Details
    ISSN: 0006-3592
    Keywords: pyrolysis mass spectrometry ; artificial neural networks ; fermentor broths ; regression analysis ; chemometrics ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Binary mixtures of model systems consisting of the antibiotic ampicillin with either Escherichia coli or Staphylococcus auresu were subjected to pyrolysis mass spectrometry (PyMS). To deconvolute the pyrolysis mass spectra, so as to obtain quantitative information on the concentration of ampicilin in the mixtures, partial least squares regression (PLS), principal components regression (PCR), and fully interconnected feedforward artificial neural networks (ANNs) were studied. In the latter case, the weights were modified using the standard backpropagation algorithm, and the nodes used a sigmoidal squsahing funciton. It was found that each of the methods could be used to provide calibration models which gave excellent predictions for the concentrations of ampicillin in samples on which they had not been trained. Furthermore, ANNs trained to predict the amount of ampicilin in E. coli were able to generalise so as to predict the concentration of ampicillin in a S. aureus background, illustrating the robustness of ANNs to rather substantial variations in the biological background. The PyMS of the complex mixture of ampicilin in bacteria could not be expressed simply in terms of additive combinations of the spectra describing the pure components of the mixtures and their relative concentrations. Intermolecular reactions took place in the pyrolysate, leading to a lack of superposition of the spectral components and to a dependence of the normalized mass spectrum on sample size. Samples from fermentations of a single organism in a complex production medium were also analyzed quantitatively for a drug of commercial interest. The drug could also be quantified in a variety of mutant-producing strains cultivated in the same medium. The combination of PyMS and ANNs constitutes a novel, rapid, and convenient method for exploitation in strain improvement screening programs. © 1994 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bit.260441008
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  • 8
    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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  • 9
    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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  • 10
    Electronic Resource
    Electronic Resource
    Ion-exchange and affinity chromatography costs in α-galactosidase purification (1992)
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 39 (1992), S. 717-724 
    Details
    ISSN: 0006-3592
    Keywords: Chromatography costs ; cost equations ; α-galactosidase ; enzyme purification ; affinity chromatography ; ion-exchange chromatography ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The purification of α-galactosidase from soybean seeds is a five to six-step procedure consisting of cryoprecipitation, acid precipitation and ammonium sulfate fractionation followed by two or three chromatography steps. The procedures, while not optimized, were carried out in a manner that resulted in 414-515-fold purification, as reported previously. The costs of two purification sequences were compared. In the best case, the preparative-scale costs of stationary phase, reagents, and hardware were $790 per million enzyme units, excluding labor. Stationary phase costs predominated over extraction, chromatography reagent, and eluent costs when the stationary phase is replaced after 10-40 cycles of use. However, if stationary phase life exceeds 50-200 cycles, stationary phase costs become similar in magnitude to eluent and reagent costs. Labor costs, which are process-specific and difficult to estimate, exceed all other costs by a factor of 10-50 at a small scale of operation and constitute a major cost, regardless of scale. This case study provides equations and a frame-work for carrying out a first comparison of costs for multistep purification sequences. Column life, throughput, and scale of operation were found to determine not only the magnitude, but also the relative contributions, of the different components that make up purification costs. This analysis shows that there are major opportunities for reducing purification costs through the development of less expensive stationary phases and the implementation of intelligent process control and automation for process scale chromatography.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bit.260390704
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