This study compares the efficiency of commercially available sorbitol-based clarifying agent (NA) and varying amounts of long chain-branched polypropylene (LCBPP) acting as a specific α-nucleating agent for linear polypropylene (PP). The sorbitol-based clarifying agent, 1,3;2,4-bis(3,4-dimethyl benzylidene)sorbitol (Millad 3988), in concentration 0.2 wt%, and LCBPP in the concentration of 1, 2, 5 and 10 wt% were mixed into PP. The comparison of the effect of NA and long branches under isothermal conditions on the crystallization process, crystallinity and polymorphic composition was realized by differential scanning calorimetry and wide-angle X-ray scattering. The addition of long chain-branched polypropylene, even at the lowest concentration, performs better at higher crystallization temperatures and has a superior effect on the crystallization process, crystallization rate and overall crystallization than the addition of NA.

In this research, a straightforward template method was utilized to fabricate a superhydrophilic ethylene-vinyl acetate copolymer (EVA)/nitrile-butadiene rubber (NBR) thermoplastic vulcanizate (TPV) surface where the paper sheet was used as template. Organic modified montmorillonite (OMMT) powder was introduced in order to improve the superhydrophilic response rate of the TPV surface. Investigations were conducted to research the durability and the self-cleaning behavior of the TPV surface, as well as to explore its potential application in the separation of oil-water and oil-oil mixtures. Experimental results demonstrated that the EVA/NBR/OMMT TPV (mass ratio 20/80/7) surface molded with No. 1000 paper sheet exhibited the excellent superhydrophilic property, which could achieve a contact angle of 0.0° within 5.5 s and had a surface energy of 35.6 mN·m^–1. The superhydrophilic surface displayed the remarkable durability and the evident self-cleaning behavior; moreover, it could exhibit the significant difference in the critical pressure data for various liquids, suggesting the promising application in the field of oil-water and oil-oil separation.

A set of linear Fischer-Tropsch (FT) waxes were oxidized to various degrees by utilizing an ozonolysis method. These waxes were comprehensively characterized in terms of their chemical composition, thermal behaviour, molecular weight distributions, and overall polarity using various analytical techniques, including Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance spectroscopy (NMR), differential scanning calorimetry (DSC), high temperature size exclusion chromatography (HT-SEC) along with normal and reverse-phase high temperature solvent gradient interaction chromatography (HT-SGIC). Application-based studies were performed by evaluating the behaviour of these waxes in unplasticized polyvinyl chloride (uPVC) formulations. Analyses included hot melt mixing, single screw extrusion, scanning electron microscopy coupled with energy dispersive X-ray spectroscopy (SEM-EDS), and torque rheometry. Through a combination of these techniques, the lubrication mechanism of these waxes could be explained by the Rabinovitch model. It was found that a combination of molecular size and degree of polarity play a vital role in the migration of the waxes and therefore ultimately impacts the fusion behaviour of the overall polyvinyl chloride (PVC) formulation. Results indicate that fusion times can greatly be altered when using oxidised waxes, and this could be promising for the development of multifunctional lubricant systems.