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Bionanocomposite films prepared with melt compounding and film blowing were evaluated for packaging applications. The nanocomposite masterbatch with 75 wt.% polylactic acid (PLA), 5 wt.% chitin nanocrystals (ChNCs) and 20 wt.% glycerol triacetate plasticizer (GTA) was melt compounded and then diluted to 1 wt.% ChNCs with PLA and polybutylene adipate-co-terephthalate (PBAT) prior to film blowing. The morphological, mechanical, optical, thermal and barrier properties of the blown nanocomposite films were studied and compared with the reference material without ChNCs. The addition of 1 wt.% ChNCs increased the tear strength by 175% and the puncture strength by 300%. Additionally, the small amount of chitin nanocrystals affected the glass transition temperature (Tg), which increased 4 °C compared with the reference material and slightly enhanced the films degree of crystallinity. The chitin nanocomposite also had lower fungal activity and lower electrostatic attraction between the film surfaces; leading to easy opening of the plastic bags. The barrier and optical properties as well as the thermal degradation of the films were not significantly influenced by the addition of chitin nanocrystals

This work presents the synthesis of new poly­(itaconate)­s containing sulfone or nitrile pendant groups through conventional radical polymerization together with their characterization and comparison with poly­(methacrylate)­s containing identical groups. Structural and thermal characterization has been carried out in terms of Fourier transform infrared spectroscopy, differential scanning calorimetry, nuclear magnetic resonance, and thermogravimetric analysis. Characterized by broad band dielectric spectroscopy (BDS), all polymers showed dielectric constant values between 7 and 10 (at 25 °C and 1 kHz) and relative low dielectric loss values (≈0.02). BDS measurements showed, for all the polymers analyzed, notorious subglass transitions even at temperatures below −100 °C, resulting in a broad temperature interval in which these polymers exhibit high dielectric constant and could work without high losses. Therefore, these materials seem to be good candidates for dielectric applications such as energy storage, among others.

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Materials that have high dielectric constants, high energy densities and minimum dielectric losses are highly desirable for use in capacitor devices. In this sense, polymers and polymer blends have several advantages over inorganic and composite materials, such as their flexibilities, high breakdown strengths, and low dielectric losses. Moreover, the dielectric performance of a polymer depends strongly on its electronic, atomic, dipolar, ionic, and interfacial polarizations. For these reasons, chemical modification and the introduction of specific functional groups (e.g., F, CN and R−S(=O)2−R´) would improve the dielectric properties, e.g., by varying the dipolar polarization. These functional groups have been demonstrated to have large dipole moments. In this way, a high orientational polarization in the polymer can be achieved. However, the decrease in the polarization due to dielectric dissipation and the frequency dependency of the polarization are challenging tasks to date. Polymers with high glass transition temperatures (Tg) that contain permanent dipoles can help to reduce dielectric losses due to conduction phenomena related to ionic mechanisms. Additionally, sub-Tg transitions (e.g., γ and β relaxations) attributed to the free rotational motions of the dipolar entities would increase the polarization of the material, resulting in polymers with high dielectric constants and, hopefully, dielectric losses that are as low as possible. Thus, polymer materials with high glass transition temperatures and considerable contributions from the dipolar polarization mechanisms of sub-Tg transitions are known as “dipolar glass polymers”. Considering this, the main aspects of this combined strategy and the future prospects of these types of material were discussed.