With the inherent demand for hydrophobic materials in processes such as membrane distillation and unidirectional moisture conduction, the preparation and application development of profiles such as modified cellulose acetate membranes that have both hydrophobic functions and biological properties have become a research hotspot. Compared with the petrochemical polymer materials used in conventional hydrophobic membrane preparation, cellulose acetate, as the most important cellulose derivative, exhibits many advantages, such as a high natural abundance, good film forming, and easy modification and biodegradability, and it is a promising polymer raw material for environmental purification. This paper focuses on the research progress of the hydrophobic cellulose acetate preparation process and its current application in the water-treatment and resource-utilization fields. It provides a detailed introduction and comparison of the technical characteristics, existing problems, and development trends of micro- and nanostructure and chemical functional surface construction in the hydrophobic modification of cellulose acetate. Further review was conducted and elaborated on the applications of hydrophobic cellulose acetate membranes and other profiles in oil–water separation, brine desalination, water-repellent protective materials, and other separation/filtration fields. Based on the analysis of the technological and performance advantages of profile products such as hydrophobic cellulose acetate membranes, it is noted that key issues need to be addressed and urgently resolved for the further development of hydrophobic cellulose acetate membranes. This will provide a reference basis for the expansion and application of high-performance cellulose acetate membrane products in the environmental field.

Wool fibers usually need shrinkproofing finishing. The enzyme process is an eco-friendly technology but the traditional exhaustion treatment usually takes excessive time. This study developed a novel multiple padding shrinkproofing process of wool with Savinase 16L and an organic phosphine compound {[HO(CH₂)_n]₃P, n ∈ (1, 10)}. SEM and XPS analyses were employed to compare the wool treated respectively by exhaustion and by padding to reveal the effect of multiple padding. The results showed that treated wool fiber achieved the requirement of machine-washable (area shrinkage less than 8% according to standard TM 31 5 × 5A) in 2.5 min by the padding process. The padding process can control the adsorbance of enzyme on wool, which makes treatment more uniform and avoids strong damage of the wool. Also, the removal efficiency of the disulfide bond was about 15 times as much as in the exhaustion treatment in 2.5 min. The average catalytic rate of the padding process was 14 times faster than the exhaustion process, and the process time (2.5 min) decreased by 32.5 min compared with the exhaustion process (35 min). Multiple padding techniques can achieve continuous production and replace the environmentally harmful chlorination process. Our results provide the underlying insights needed to guide the research of the enzyme process application.

Much research has focused on improvement of the structural and mechanical properties of regenerated keratin materials by physical or chemical methods in recent years. In this research, regenerated keratin materials were modified with graphene oxide (GO). The properties of modified keratin films and the mechanism of interaction between GO and keratin macromolecules were studied. The SEM and XRD test results showed that the orientation of keratin macromolecules could be effectively improved by GO, which favored improvement of the keratin material’s crystallinity and made the films more uniform and compact. The thermal stability and mechanical properties of GO-modified keratin films were also improved significantly. At the same time, the reaction mechanism between keratin and GO materials was analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), FT-IR, and Raman spectroscopy. It was shown that there was no chemical reaction between GO and keratin molecules, and the interaction between them was mainly via hydrogen bonding and van der Waals forces.

The hydrolytic destruction of wool scales using a protease catalyzed system is a point-to-surface process. The surface zeta potential of wool fibers increased after treatment, and disulfide bonds were broken, which was more favorable for dyeing.