1962
DOI: 10.1002/macp.1962.020570112
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Die Adsorption von Makromolekeln IV. Mehrschichtenadsorption von Polyäthylenglykolen

Abstract: zum 60. Geburtstag in Verehrung gewidmet (Eingegangen am 27. Juli 1962) ZUSAMMENFASSUNG:Mit Polyathylenglykolen der Molekulargewichte 1000-28 000 wurden Adsorptionsmessungen aus Losung durchgefiihrt. Die an Folien adsorbierte Menge wird durch Wagung bestimmt, ohne dabei einen Eingriff in das MeRsystem vorzunehmen. E s ergeben sich stufenformige Adsorptionsisothermen, deren Abhangigkeit von Temperatur und Molekulargewicht in verschiedenen Losungsmittel/Adsorbenssystemen zu interessanten Aufschliissen iiber die … Show more

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Cited by 16 publications
(2 citation statements)
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“…In thermodynamic terms, polymer adsorption was treated like that of low-molecular-weight solutes, for which Langmuir-type kinetics and equilibria had been found to apply (5,6). Adsorption enthalpy was for example derived from the temperature dependence of adsorption isotherms (7)(8)(9). Killmann pointed out that this method might cause problems insofar as the conditions of isostericity and reversibility were not fulfilled in the case of polymer adsorption and showed that contradictory results were obtained using the Clausius-Clapeyron equation or direct measurements of adsorption enthalpy (10).…”
Section: Introductionmentioning
confidence: 99%
“…In thermodynamic terms, polymer adsorption was treated like that of low-molecular-weight solutes, for which Langmuir-type kinetics and equilibria had been found to apply (5,6). Adsorption enthalpy was for example derived from the temperature dependence of adsorption isotherms (7)(8)(9). Killmann pointed out that this method might cause problems insofar as the conditions of isostericity and reversibility were not fulfilled in the case of polymer adsorption and showed that contradictory results were obtained using the Clausius-Clapeyron equation or direct measurements of adsorption enthalpy (10).…”
Section: Introductionmentioning
confidence: 99%
“…Conformational distortion into a rather elongated state has been supported by experimental measurements19 of the fraction of functional groups attached to the surface (e.g., more than 30%). The effect of solution variables (solvent, temperature, and molecular weight) and nature of the substrate on amount adsorbed has also been investigated (e.g., see ref [20][21][22][23][24][25][26][27]. Even though there are exceptions, adsorption usually increases with molecular weight, and it is inversely proportional to solution intrinsic viscosity (it decreases with solvent power).…”
Section: Introductionmentioning
confidence: 99%