The importance of doping TiO2 into polypyrrol nanofibers to improve their optical sensitivity

In this study Electrochemical polymerization was used to make polypyrrol nanofiber. The in situ chemical oxidative polymerization approach was used to create a nanocomposite of polypyrrole PPy-TiO2. To achieve homogeneous dispersion inside the PPy matrix, the TiO2 was dissolved and ultrasonically dispersed. The surface morphology of polypyrrol and PPy/TiO2 nanocomposites was studied using field emission scanning electron microscopy (FE-SEM), which revealed of a polypyrrol nanofibre network and showed that the TiO2 nanoparticles was well incorporated. The produced PPy/TiO2 nanocomposite was characterized using XRD (X-Ray diffraction) and FT-IR (Fourier Transform Infrared). The formation of TiO2 nanoparticales on a PPy layer matrix was discovered, as well as homogeneous dispersion of TiO2 inside the PPy matrix and considerable interaction between PPy and TiO2. The produced PPy/TiO2 nanocomposite sensors’ response was investigated towards of light-power sensitivity. The PPy/TiO2 synergistic effects improve the light sensitivity qualities of the photodetector. The maximium sensitivity of PPy/TiO2 was around (188 %) at 20% TiO2 concentration at a light power of 30 mW for a laser diode 720 nm, while the rise time and fall time was ≈ 2.5sec.

Biodegradable Poly(Butylene Adipate-Co-Terephthalate) and Thermoplastic Starch-Blended TiO2 Nanocomposite Blown Films as Functional Active Packaging of Fresh Fruit

Biodegradable polymers can be used for eco-friendly, functional, active packaging to preserve food quality. Incorporation of titanium dioxide (TiO2) nanoparticles into polymer packaging enhances ethylene-scavenging activity and extends the shelf-life of fresh produce. In this study, TiO2 nanoparticles were incorporated into biodegradable poly(butylene adipate-co-terephthalate) (PBAT)- and thermoplastic cassava starch (TPS)-blended films to produce nanocomposite packaging via blown-film extrusion. The effects of TiO2 on morphology, packaging properties, and applications as functional packaging for fresh produce were investigated. Increased TiO2 in the film packaging increased amorphous starch content and hydrogen bonding by interacting with the TPS phase of the polymer blend, with negligible chemical interaction with the PBAT component and identical mechanical relaxation in the PBAT phase. Surface topography indicated void space due to non-homogeneous dispersion causing increased oxygen and carbon dioxide permeability. Homogeneous dispersion of fine TiO2 nanoparticles increased mechanical strength and reduced oxygen, carbon dioxide, and water vapor permeability. Films containing TiO2 also showed efficient oxygen-scavenging activity that removed residual oxygen from the package headspace dependent on the levels and morphology of nanoparticles in the film matrices. Banana fruit packaged in films containing TiO2 recorded slower darkening color change and enhanced shelf-life with increasing TiO2 content.

Beyond homogeneous dispersion: oriented conductive fillers for high κ nanocomposites

Rational design of structures for regulating the thermal conductivities (κ) of materials is critical to many components and products employed in electrical, electronics, energy, construction, and aerospace, as well as...

Impact of Polymer Binders on the Structure of Highly Filled Zirconia Feedstocks

The impact of polypropylene and high-density polyethylene backbone binders on the structure of organic matrix, feedstock, and ceramic parts is investigated in terms of morphology in this paper. The miscibility of wax with polyethylene and polypropylene is investigated in the molten state via a rheological study, revealing wax full miscibility with high-density polyethylene and restricted miscibility with polypropylene. Mercury porosimetry measurements realized after wax extraction allow the characterization of wax dispersion in both neat organic blends and zirconia filled feedstocks. Miscibility differences in the molten state highly impact wax dispersion in backbone polymers after cooling: wax is preferentially located in polyethylene phase, while it is easily segregated from polypropylene phase, leading to the creation of large cracks during solvent debinding. The use of a polyethylene/polypropylene ratio higher than 70/30 hinders wax segregation and favors its homogeneous dispersion in organic binder. As zirconia is added to organic blends containing polyethylene, polypropylene, and wax, the pore size distribution created by wax extraction is shifted towards smaller pores. Above zirconia percolation at 40 vol%, the pore size distribution becomes sharp attesting of wax homogeneous dispersion. As the PP content in the organic binder decreases from 100% to 0%, the pore size distribution is reduced of 30%, leading to higher densification ability. In order to ensure a maximal densification of the final ceramic, polyethylene/polypropylene ratios with a minimum content of 70% of high-density polyethylene should be employed.