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  • Cryofixation  (1)
  • Gallstone formation  (1)
  • Key words Cationic surfactant rheology–counterion/surfactant ratio–surfactant drag reduction–cationic surfactant microstructure  (1)
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  • 1
    ISSN: 0014-5793
    Keywords: Bile ; Cholesterol ; Crystallization ; Gallstone formation
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1435-1528
    Keywords: Key words Cationic surfactant rheology–counterion/surfactant ratio–surfactant drag reduction–cationic surfactant microstructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract Rheology, drag reduction and cryo-TEM experiments were performed on Arquad 16–50/NaSal and Ethoquad O/12/NaSal surfactant systems at different counterion-to-surfactant ratios and at constant low surfactant concentrations, 5 mM, appropriate for drag reduction. The molar ratio of counterion-to-surface was varied from 0.6 to 2.5. All the surfactant systems described here are viscoelastic and drag reducing. The viscoelasticity and drag reducing effectiveness increase with increase in counterion/surfactant ratio. Network are present in the solutions with high ratio, and they are viscoelastic. However, shear is needed to induce network formation for solutions at low ratio. Cryo-TEM images confirm the existence of thread-like micelles which form entanglement networks, and show that the micellar network becomes denser with increasing counterion/surfactant ratio in one surfactant series. Both increase in the counterion/surfactant ratio and increase in the shear rate result in shorter relaxation times. For some of these systems, abrupt increase in viscosity is observed at certain shear rates which are time effects affecting microstructure rearrangements rather than formation of shear induced structures.
    Type of Medium: Electronic Resource
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  • 3
    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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