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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 18 (1979), S. 3177-3179 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 51 (1979), S. 717-722 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 51 (1979), S. 712-717 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1471-0528
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Cambridge : Cambridge University Press
    Greece and Rome 15 (1946), S. 33-41 
    ISSN: 0017-3835
    Source: Cambridge Journals Digital Archives
    Topics: Archaeology , Classical Studies
    Notes: In the somewhat unusual situation of a mathematician invited to address a Classical Society, there is one question which I am forced to put to myself. Can anything of interest to present-day students of the Classics survive from a modest Classical course taken over forty years ago, and followed by a lifetime of activity in a very different academical groove? Any slight merit which the following remarks may possess will arise from their character as a personal testimony.I begin by putting a question to you. What influences led you to take up a course in Classics at college? I can imagine many possible contributory causes: the accident of the particular school you attended, high success in your School Certificate Examination, a real pleasure in getting up the rudiments of Latin or Greek grammar; or a teacher who bound you with a spell and gave you glimpses of romance. Whatever the cause, you have made the choice, and, like all choices, it imposes a limitation. To some extent, and at least for a time, you are debarred from specializing in some other subject: Philosophy or Modern Languages, Physics or Biology. You are approaching the vast unity of human knowledge and achievement from a specific angle, and along a very definite path.Pascal, the great literary, scientific, and religious genius of seventeenth-century France, has a fine saying: ‘The whole succession of men through the ages should be considered as one man, ever living and always learning.’ The unity of human knowledge and achievement cannot be broken up without serious loss.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of food science 45 (1980), 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: Studies were carried out on the effect of low voltage stimulation of beef carcasses on the onset of rigor mortis and meat tenderness. One side of each of 14 beef carcasses was electrically stimulated using a step-wise increase in voltage to a peak of 32V direct current; the other side being used as the unstimulated control. Application of this low voltage treatment produced marked muscle contraction and carcass distortion. The rate of fall of muscle pH (indicating the onset of rigor mortis) was appreciably more rapid in the stimulated than the control sides. Meat samples from stimulated sides assessed by the use of objective and subjective methods were found to be significantly (P 〈 0.01) more tender than samples from unstimulated sides. The data suggest that low voltage stimulation (32V) of beef carcasses was associated with hastening of rigor mortis and improvement in tenderness comparable to that reported for carcasses subjected to voltages between 11OV and 3600V.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 40 (1994), S. 321-333 
    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 mathematical model has been developed to predict the coupled hydrodynamics and high-molecular-weight protein transport in mammalian-cell hollow-fiber bioreactors (HFBRs). The analysis applies to reactors with isotropic ultrafiltration membranes under startup conditions when the extracapillary space (ECS) is essentially unobstructed by cells. The model confirms the experimental finding that secondary ECS flows, engendered by the primary flow in the fiber lumens, can cause significant downstream polarization of ECS proteins at typical mammalian-cell HFBR operating conditions. It also reveals that the osmotic activity of the proteins, by curtailing transmembrane fluid fluxes, can influence strongly the outcome of the polarization process. In fact, at order-of-magnitude higher protein concentrations and/or lower recycle flow rates, the secondary flow velocities can be reduced by as much as six orders-of-magnitude throughout the ECS, thereby virtually eliminating the polarization problem. This result has important implications for improved reactor startup procedures.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1133-1145 
    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: Polyurethanes are one of the most important classes of thermoplastic elastomers and have been widely used in medical-device manufacturing as well as in other applications. However, their function can be limited, particularly under environmental conditions that render them susceptible to hydrolysis. Using polymeric additives that are hydrolytically stable may be one approach to modifying the surface of polyurethanes for the purpose of improving their hydrolytic resistance without compromising their structural features. In this paper, the development of a series of novel fluorine-containing polyurethane surface modifying macromolecules (SMMs) is described and their synthesis conditions are investigated. The material structure and mixing properties of the synthesized SMMs with base polyurethanes was dependent on the reactant stoichiometry and concentration for the SMM components, as well as the reaction temperature and the amount of catalyst used in the SMM synthesis. This study describes the use of low surface energy components (fluorinated tails) which showed selective migration towards the surface when added to a polyester-urea-urethane. These novel macromolecules generated a nonwettable surface while not significantly altering the apparent bulk structure of the base polymer. The advancing and receding contact angle results indicated that the surface of these modified polyurethanes showed wettability characteristics similar to that of Teflon. TM The differential scanning calorimetry thermograms for the mixtures of the SMM with the polyurethane showed that, at 5% w/w SMM in the base polyurethane, the thermal transitions were similar to that of the native base polyure-thane, indicating that the additives had no detectable effect on the polyurethane structure. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 35 (1997), S. 371-381 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Polyurethanes are widely used as biomaterials for medical implants because of their excellent mechanical properties and moderate biocompatibility. However, the demand for more bioresistant and biocompatible polyurethanes to meet the needs of long-term implant devices still remains an important issue. Since most biological interactions with materials occur at the interface, a significant number of studies for improving the biocompatibility of polyurethanes have concentrated on surface modification. It is well known that additives used in polymeric materials as processing aids, mold releasing agents, antioxidants, etc., migrate to the surface and change the surface properties of the material. Under certain conditions polymeric additives may also migrate toward surfaces. This study describes two fluorine-containing, surface-modifying macromolecules (SMMs) that have been evaluated for their ability to inhibit polyurethane degradation. These materials actively migrate to the upper surface of a material film when they are mixed with a base polymeric material. Contact angle measurements for the mixture of SMM with base polyurethane indicate that the surface becomes more hydrophobic after adding the SMMs, while X-ray photoelectron spectroscopy analysis shows an enrichment of fluorine on the polymer surfaces. Differential scanning calorimetry thermograms indicate that the microstructure, as defined by the thermal transitions of the base polymer, are not altered by the addition of SMMs. Enzyme-induced biodegradation tests exhibit a significant reduction of polyurethane degradation in the presence of these surface-resident materials. The results indicate that the SMMs have the potential to resist hydrolytic degradation mediated by lysosomal enzymes while generating a surface chemistry on the native elastomer which is similar in nature to that of a fluoropolymer, e.g., Teflon. © 1997 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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