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Molecular origin of the foam structure in model linear and comb polystyrenes: II. Volume expansion ratio

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Abstract The effect of the molecular architecture of a series of anionically synthesized linear and comb atactic polystyrenes (PS) on their foam properties including cell size, cell density, and volume… Click to show full abstract

Abstract The effect of the molecular architecture of a series of anionically synthesized linear and comb atactic polystyrenes (PS) on their foam properties including cell size, cell density, and volume expansion ratio (V.E.R.) was investigated. The comb-PS had the same molecular weight of the backbone, Mw,bb ≈ 290 kg/mol, Zbb ≈ 20 entanglements, and branches, Mw,br ≈ 44 kg/mol, Zbr ≈ 3 entanglements, but different numbers of branches, 3 ≤ Nbr ≤ 190. Batch foaming of well-purified linear and comb-PS using CO2 resulted in cell densities about 109 and 4 × 109 cell/cm3, respectively, which shows that LCB has no distinct effect on the cell density, whereas a small amount of residual impurity in linear PS reduced the cell density to ~108 cell/cm3. For a comb-PS series with the same entangled backbone, Mw,bb ≈ 290 kg/mol, Zbb ≈ 20 entanglements, and similar branches, Mw,br ≈ 44 kg/mol, Zbr ≈ 3 entanglements, but different numbers of branches, 3 ≤ Nbr ≤ 190, an increase in the Nbr to 120 with densely grafted comb conformation gradually increased the highest achievable V.E.R. close to a theoretical limit given by the CO2 solubility. The further increase of Nbr to 190 with a bottlebrush conformation reduced the V.E.R. of the foam. From a rheological point of view, this optimum Nbr was related to a comb-PS which showed the maximum strain hardening factor (SHF ≈ 200) in uniaxial extension, and simultaneously the minimum in the zero shear viscosity, η0. The optimum Nbr = 120 for this comb-PS series corresponds to an average spacing distance between two neighbor branch points of about Zs ≈ 0.2 entanglements.

Keywords: foam; volume expansion; expansion ratio; linear comb; cell; comb

Journal Title: Polymer
Year Published: 2020

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