Recycled waste industrial cellulose triacetate (TAC) film, which is one of the key materials in polarizers, was used to produce nanofiber membranes by electrospinning and synergistic assembly with graphene oxide (GO) and titanium dioxide (TiO₂) for oil-water separation. In this study, GO and TiO₂ coated by an electrophoretic deposition method introduced super hydrophilicity onto the recycled TAC (rTAC) membrane, with enhanced water permeability. The results indicate that when the outermost TiO₂ layer of an asymmetric composite fiber membrane is exposed to ultraviolet irradiation; the hydrophilicity of the hydrophilic layer is more effectively promoted. Moreover, this coating could efficiently repel oil, and demonstrated robust self-cleaning performance during the cycle test, with the aid of the photocatalytic properties of TiO₂. The rTAC membrane of networked hydrophobic fibers could also increase the speed of the filtrate flow and the water flux of the oil-water emulsion. The permeate carbon concentration in the water was analyzed using a total organic carbon analyzer. Incorporation of TiO₂/GO onto the rTAC membrane contributed greatly towards enhanced membrane hydrophilicity and antifouling performance. Therefore, the novel TiO₂/GO/rTAC asymmetric composite fiber has promise for applications in oil-water separation.

In this study, a long carbon chain dimer acid is introduced into a nylon 6 structure and is copolymerized with different structural amines to produce amorphous nylon 6 by 4,4′-methylenebis(2-methylcyclohexylamine) (MMCA) in different copolymerization ratios. The effect of different structures and copolymerization ratios on the properties of nylon 6 is determined, along with the thermal properties, crystallinity, water absorption, dynamic mechanical properties, and optical properties. It is found that the melting point and the thermal cracking temperature Td10 of nylon 6 are respectively between 176 °C and 213 °C and 378 °C to 405 °C. The effect of introducing a bicyclohexane group containing a methyl side chain is greater than that of a meta-benzene ring, so COMM (synthesized by Caprolactam (C), dimer oleic acid (OA), and 4,4′-Methylenebis(2-methylcyclohexylamine) (MMCA)) has the lowest melting point, enthalpy, and crystallinity. As the copolymerization ratio increases, its thermal properties decrease. 10% is the lowest crystallinity. The amine structure containing a bicycloalkyl group has lower water absorption and a 10% copolymerization ratio gives the lowest water absorption. It contains the bicycloalkyl group, COM (synthesized by Caprolactam (C), dimer oleic acid (OA) and 4,4′-Methylenebis(cyclohexylamine) (MCA)), which has the highest loss modulus. The lowest loss modulus is noted for a copolymerization ratio of 7% and the value of tan δ increases as the copolymerization ratio increases. The introduction of nylon 6 with the bicycloalkyl groups, COMM and COM, significantly increases transparency. As the copolymerization ratio increases, the transparency increases and the haze decreases. The best optical properties are achieved for 10% copolymerization.

The triacetin and nitroglycerin barrier properties of layered-silicate reinforced ethylenepropylenediene monomer/chloroprene rubber (EPDM/CR) nanorubbers were investigated as rocket-propellant inhibitors. EPDM/CR nanorubbers with intercalated structures were formulated and prepared by the melt-compounding method. The triacetin permeability and nitroglycerin absorption were observed to decrease with increasing layered-silicate content. The layered silicates also improved the flame retardancies of the nanorubbers by forming silicate reinforced carbonaceous chars. Layered-silicate reinforced EPDM/CR nanorubbers are potentially effective rocket propellant-inhibiting materials.