Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 275 (1997), S. 1018-1026 
    ISSN: 1435-1536
    Keywords: Key words Water ; desorption ; multilayer adsorption ; water structure ; water cooperativity ; H-bonds ; IR spectroscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  The structure of water adsorbed in cellulose acetate membranes is determined by the fundamental and overtone IR spectra. Water is weakly H-bonded to ester and ether groups of the membrane, at low water contents. With increasing water content, more and more liquid-like water is observed. In addition, a small amount of a third type of water is present. The amounts of these three species are estimated from the spectra. At high water contents, the amount of liquid-like water increases strongly. The H-bond cooperativity of such water may be the cause for this increase and for the common anomalous water adsorption isotherms. The H-bond energy of the first hydration shell is relatively small, contrary to the anomalous large adsorption heats ΔH ad. This could be described by larger van der Waals interactions between this type of water and the membrane groups as a result of a higher coordination number compared with Z=4.4 of liquid-like water. This model is in agreement with the decrease of ΔH ad with increasing water sorption reaching the evaporization enthalpy of pure water at high water contents.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 275 (1997), S. 964-971 
    ISSN: 1435-1536
    Keywords: Key words Membranes ; water desorption ; desorption heat ; adsorption mechanism ; multilayer adsorption ; partition coefficients ; water cooperativity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  The water desorption isotherms are determined in three cellulose acetate membranes with different acetyl content as a function of p/p 0 at 10–40 °C. The partition coefficients (adsorbed water over water pressure) show a minimum at p/p 0=0.5–0.6. This indicates a two energy mechanism. The agreement of our results with the BET adsorption isotherms only till p/p 0〈0.3 shows that a two energy adsorption mechanism is valid only for small water contents, probably one hydrate layer and a second more liquid-like water layer. At large p/p 0, the adsorbed water becomes more and more liquid like by polarization of the hydrogen bonds. The heat of desorption is larger than the vaporization heat of water ΔH vap(H2O). It decreases with increasing water content asymptotically to ΔH vap(H2O). The cause may be a larger van der Waals interaction of the hydrate layer due to coordination numbers larger than 4.4 as in liquid water. Additionally, we found a hole adsorption process by sorbing unpolar solvents. The water and methonal adsorption are 100 times larger due to a swelling mechanism depending on the number of acetyl groups in the membranes. The amounts of n-alcohols sorbed decrease with their chain length.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...