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In this study, two ionic liquids (IL) with different anions (decanoate, tetrafluoroborate) but with the same phosphonium-based cation were evaluated as potential plasticizers and lubricants for polylactic acid (PLA). Both ILs at 5 wt% were well dispersible and partly miscible with PLA as evidenced by scanning electron microscopy, SEM, and glass transition temperature, T g , characterization, as well as from solubility parameters calculations. However, phase separation in the PLA system containing the IL with tetrafluoroborate anions was observed 1 year after melt processing. The IL containing the tetrafluoroborate anion showed higher thermal stability compared with the IL containing decanoate as confirmed by thermogravimetric analysis. This was translated in corresponding behaviors of the PLA blends. The effects of the IL containing the tetrafluoroborate anion were more pronounced on lubrication as evidenced by lower values of coefficient of friction that could also be correlated with lower contact angle; this IL could then be considered as a more effective, overall, plasticizer than the IL containing the decanoate anion based on reduced flexural modulus and brittleness as well as T g suppression results. The extent of plasticization, however, could also be related to the molecular weight reduction during melt processing that occurred in the presence of both ILs, but to different degrees.

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Cationic nanoclays were treated by ion exchange with various ionic liquids (ILs) containing cations and anions of different structure and/or molecular weight in order to investigate the effects of the IL structure and cation chain length on extent of clay dispersion, intercalation, and thermal stability. The modified clays containing imidazolium‐, pyridinium‐, and phosphonium‐based cations were characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, and X‐ray diffraction. Although the thermal stability of pure ILs was mostly controlled by the type of the anion present, high temperature thermal stability of the modified clays, at the IL cation loadings achieved in this work, was not significantly dependent on type, structure, or size of the cation. The latter parameters, however, were of significant importance in controlling degree of dispersion of the nanoclays during melt compounding with polypropylene (PP). Basal spacing increased proportionally to the size and type of the intercalated cations and showed little change in the PP composites. Although commercial organoclays were shown to be less thermally stable than IL modified clays, they exhibited larger basal spacing and better dispersion characteristics in the polyolefin matrix; however, they increased to the same extent the thermal stability of the PP matrix as the phosphonium modified clays. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers

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