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Effect of graft density on the nonionic bottle brush polymer/surfactant interaction

Varga, Imre (författare)
KTH,Yt- och korrosionsvetenskap
Mezaros, R (författare)
Makuska, R (författare)
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Claesson, Per M. (författare)
KTH,RISE,YKI – Ytkemiska institutet,Yt- och korrosionsvetenskap
Gilanyi, T (författare)
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 (creator_code:org_t)
2009-09-09
2009
Engelska.
Ingår i: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 25:19, s. 11383–11389-
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The effect of graft density on the interaction of nonionic bottle brush polymers with an anionic surfactant (sodium dodecyl sulfate) was investigated. The graft density of 45 units long poly(ethylene oxide) (PEO) side chains was varied in a wide range (30, 50, 75, 90, and 100%) on a methacrylate type polymer backbone. The surfactant binding isotherms were determined by the potentiometric method in the presence of 0.1 M sodium bromide. It was found that due to the grafting of the PEO chains to a polymer backbone the surfactant binding becomes significantly suppressed. The amount of bound surfactant at the critical micelle concentration (cmc) decreases almost 2 orders of magnitude compared to the binding on a linear PEO having a similar molecular weight. The binding of the surfactant was found to occur in cooperative fashion, though the critical aggregation concentration (cac) of the binding was found surprisingly small. This result was interpreted in terms of the surfactant aggregation numbers that were found much smaller in the case of the bottle brush polymers than in the case of linear PEOs due to the steric crowding of the grafted PEO chains. To confirm the results of the binding isotherm measurements, steady-state fluorescence probe (pyrene) measurements as well as static and dynamic light scattering measurements were performed.

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