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  • Cell & Developmental Biology  (2)
  • Constitutive model  (1)
  • Cryofixation  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 34 (1995), S. 209-214 
    ISSN: 1435-1528
    Keywords: Constitutive model ; flow-sensitive viscosity ; complex flow modelling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract A new class of inelastic constitutive equations is presented and discussed. In addition to the rate-of-strain tensor, the stress is assumed to depend also on the relative-rate-of-rotation tensor, a frame-indifferent quantity that brings information about the nature of the flow. The material functions predicted by these constitutive equations are given for simple shear and uniaxial extension. A special case of these equations takes the Newtonian form, except that the viscosity is a function of the invariants of both kinematic tensors on which the stress depends. This simple constitutive equation has potential applications in liquid flow process simulations, since it combines simplicity with the capability of responding independently to shear and extension, as real liquids seem to do. Finally, possible forms for the new viscosity function are discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 10 (1988), S. 87-111 
    ISSN: 0741-0581
    Keywords: Cryo-electron microscopy ; Cryofixation ; Vitreous ice ; Plunge-cooling ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: The controlled environment vitrification system (CEVS) permits cryofixation of hydrated biological and colloidal dispersions and aggregates from a temperature- and saturation-controlled environment. Otherwise, specimens prepared in an uncontrolled laboratory atmosphere are subject to evaporation and heat transfer, which may introduce artifacts caused by concentration, pH, ionic strength, and temperature changes. Moreover, it is difficult to fix and examine the microstructure of systems at temperatures other than ambient (e.g., biological systems at in vivo conditions and colloidal systems above room temperature). A system has been developed that ensures that a liquid or partially liquid specimen is maintained in its original state while it is being prepared before vitrification and, once prepared, is vitrified with little alteration of its microstructure. A controlled environment is provided within a chamber where temperature and chemical activity of volatile components can be controlled while the specimen is being prepared. The specimen grid is mounted on a plunger, and a synchronous shutter is opened almost simultaneously with the release of the plunger, so that the specimen is propelled abruptly through the shutter opening into a cryogenic bath. We describe the system and its use and illustrate the value of the technique with TEM micrographs of surfactant microstructures in which specimen preparation artifacts were avoided. We also discuss applications to other instruments like SEM, to other techniques like freeze-fracture, and to novel “on the grid” experiments that make it possible to freeze successive instants of dynamic processes such as membrane fusion, chemical reactions, and phase transitions.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 3 (1986), S. 385-400 
    ISSN: 0741-0581
    Keywords: Freeze fractures ; Vesicles ; Liquid crystal ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: A computer-aided graphics approach to correlating transmission electron microscope images of freeze-fractured and thin-sectioned samples is outlined. Any three-dimensional model of the imaged structure can be mathematically sectioned to provide a two-dimensional representation of the model in the “fracture” plane. The method is used to demonstrate that the structure of lamellar liquid crystalline liposomes is based on a family of Dupin cyclides; closed, parallel surfaces with a conjugate ellipse and hyperbola as curvature defects.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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