Carbon dioxide foaming and high-pressure rheology of polystyrene and polystyrene/organoclay nanocomposites
Abstract (Summary)
The polymer foam industry is slowly implementing carbon dioxide (CO2) as a
low-cost, safe, and environmentally friendly blowing agent alternative to fluorocarbons
and hydrocarbons. Progress is slow due to several obstacles, ranging from low blowing
agent solubility to a lack of quantitative understanding of the influence of carbon dioxide
on viscosity.
A crucial property in foam extrusion is viscosity. Several research groups have
published viscosity data of polymer melts under high pressure, using a variety of
techniques. However, few studies assist in designing polymer processing equipment
because most do not contain predictive scaling (e.g., WLF-analogous scaling factors) to
apply to different operating conditions.
A new high-pressure rotational rheometer has been applied to polystyrene and
carbon dioxide at five concentrations. It provides direct measurement of the zero shear
viscosity of the polymer under a high pressure diluent. The method allows many viscosity
measurements to be performed on a single sample. Scaling factors are applied to the data
and the WLF-Chow equation is found to describe the results when the appropriate
parameter is selected.
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Due to an interest in using organoclay nanoparticles for foaming, the viscosity of
the polystyrene-nanoclay-CO2 system is studied using the couette rheometer and an
extruder slit die. At high shear rates (10 to 100 s-1), the viscosity of polystyrene-nanoclay-
CO2 unexpectedly possesses a lower viscosity than polystyrene-CO2 at the same
concentration. At low shear rates (10-3 to 1 s-1), this effect is not observed. It is suspected
that interfacial slip is occurred at the interface at high shear rates.
Polymer additives allow tuning of bubble morphology without changing operating
conditions. In this study, either a second polymer or nanoparticles are studied. Poly
(methyl methacrylate) (PMMA) has the ability to drastically reduce cell size of
polystyrene (PS) foams. It is believed that heterogeneous nucleation occurs at the
interface of PS/PMMA, but that the bubbles are able to grow out of both phases
simultaneously.
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Bibliographical Information:
Advisor:
School:The Ohio State University
School Location:USA - Ohio
Source Type:Master's Thesis
Keywords:plastic foams polystyrene polymers carbon dioxide nucleation supercritical fluids nanoparticles thermoplastic composites
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