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Dynamic surface properties of solutions of poly(ethylene oxide) and polyethylene glycols. / Noskov, B. A.; Akentiev, A. V.; Loglio, G.; Miller, R.

In: Journal of Physical Chemistry B, Vol. 104, No. 33, 24.08.2000, p. 7923-7931.

Research output: Contribution to journal › Article › peer-review

Harvard

Noskov, BA, Akentiev, AV, Loglio, G & Miller, R 2000, 'Dynamic surface properties of solutions of poly(ethylene oxide) and polyethylene glycols', Journal of Physical Chemistry B, vol. 104, no. 33, pp. 7923-7931.

APA

Noskov, B. A., Akentiev, A. V., Loglio, G., & Miller, R. (2000). Dynamic surface properties of solutions of poly(ethylene oxide) and polyethylene glycols. Journal of Physical Chemistry B, 104(33), 7923-7931.

Vancouver

Noskov BA, Akentiev AV, Loglio G, Miller R. Dynamic surface properties of solutions of poly(ethylene oxide) and polyethylene glycols. Journal of Physical Chemistry B. 2000 Aug 24;104(33):7923-7931.

Author

Noskov, B. A. ; Akentiev, A. V. ; Loglio, G. ; Miller, R. / Dynamic surface properties of solutions of poly(ethylene oxide) and polyethylene glycols. In: Journal of Physical Chemistry B. 2000 ; Vol. 104, No. 33. pp. 7923-7931.

BibTeX

@article{2c7285e6a42d415da5467c0d513aa58e,
title = "Dynamic surface properties of solutions of poly(ethylene oxide) and polyethylene glycols",
abstract = "The damping coefficient and the length of transversal (at the frequencies from 100 to 300 Hz) and longitudinal (at the frequencies from 0.1 to 3 Hz) surface waves have been measured as a function of the concentration of solutions of poly(ethylene glycol)s (PEG) and poly(ethylene oxide) (PEO), and the molecular weight of the polymer. A local maximum of the damping coefficient of transversal waves has been discovered for dilute solutions of PEG 400. This maximum disappears and the damping coefficient decreases monotonically with the concentration of polymers of higher molecular weight in the region of dilute solutions. A fast increase of the damping with concentration has been discovered for semidilute solutions. These experimental data are used for the calculation of the real and imaginary components of the dynamic surface elasticity as a function of concentration and frequency. The obtained dependencies can be explained with the help of a dynamic model of the surface layer of polymer solutions where the main relaxation processes are connected with the monomer exchange between different regions of the surface layer. In the investigated concentration range, the corresponding relaxation time determined from the experimental data changes by more than 2 orders of magnitude.",
author = "Noskov, {B. A.} and Akentiev, {A. V.} and G. Loglio and R. Miller",
year = "2000",
month = aug,
day = "24",
language = "English",
volume = "104",
pages = "7923--7931",
journal = "Journal of Physical Chemistry B",
issn = "1520-6106",
publisher = "American Chemical Society",
number = "33",

}

RIS

TY - JOUR

T1 - Dynamic surface properties of solutions of poly(ethylene oxide) and polyethylene glycols

AU - Noskov, B. A.

AU - Akentiev, A. V.

AU - Loglio, G.

AU - Miller, R.

PY - 2000/8/24

Y1 - 2000/8/24

N2 - The damping coefficient and the length of transversal (at the frequencies from 100 to 300 Hz) and longitudinal (at the frequencies from 0.1 to 3 Hz) surface waves have been measured as a function of the concentration of solutions of poly(ethylene glycol)s (PEG) and poly(ethylene oxide) (PEO), and the molecular weight of the polymer. A local maximum of the damping coefficient of transversal waves has been discovered for dilute solutions of PEG 400. This maximum disappears and the damping coefficient decreases monotonically with the concentration of polymers of higher molecular weight in the region of dilute solutions. A fast increase of the damping with concentration has been discovered for semidilute solutions. These experimental data are used for the calculation of the real and imaginary components of the dynamic surface elasticity as a function of concentration and frequency. The obtained dependencies can be explained with the help of a dynamic model of the surface layer of polymer solutions where the main relaxation processes are connected with the monomer exchange between different regions of the surface layer. In the investigated concentration range, the corresponding relaxation time determined from the experimental data changes by more than 2 orders of magnitude.

AB - The damping coefficient and the length of transversal (at the frequencies from 100 to 300 Hz) and longitudinal (at the frequencies from 0.1 to 3 Hz) surface waves have been measured as a function of the concentration of solutions of poly(ethylene glycol)s (PEG) and poly(ethylene oxide) (PEO), and the molecular weight of the polymer. A local maximum of the damping coefficient of transversal waves has been discovered for dilute solutions of PEG 400. This maximum disappears and the damping coefficient decreases monotonically with the concentration of polymers of higher molecular weight in the region of dilute solutions. A fast increase of the damping with concentration has been discovered for semidilute solutions. These experimental data are used for the calculation of the real and imaginary components of the dynamic surface elasticity as a function of concentration and frequency. The obtained dependencies can be explained with the help of a dynamic model of the surface layer of polymer solutions where the main relaxation processes are connected with the monomer exchange between different regions of the surface layer. In the investigated concentration range, the corresponding relaxation time determined from the experimental data changes by more than 2 orders of magnitude.

UR - http://www.scopus.com/inward/record.url?scp=0034710437&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0034710437

VL - 104

SP - 7923

EP - 7931

JO - Journal of Physical Chemistry B

JF - Journal of Physical Chemistry B

SN - 1520-6106

IS - 33

ER -

ID: 42840020