Pineapple peel cellulose nanofibrils (PCNFs) were facilely prepared by the ball milling method assisted by alkali solution (3 wt% NaOH) and a wet grinding medium, using various treated pineapple peels (hot water treatment (WT), bleaching treatment (BT), alkaline treatment (AT), and baleaching–alkaline treatment (ABT)) as raw materials. The structure of the obtained PCNFs (i.e., WT-PCNF, BT-PCNF, AT-PCNF, and ABT-PCNF) was characterized to analyze the influence of component intervention. The results indicated that NaOH-assisted ball milling did not change the crystal structure of cellulose, and the yield and thermal stability of the PCNFs was improved. The average diameters of WT-PCNF, BT-PCNF, AT-PCNF, and ABT-PCNF were 24.16, 21.53, 23.04, and 19.46 nm, respectively, in which BT-PCNF and ABT-PCNF exhibited a higher defibrillating degree and smaller diameter. Particularly, NaOH-assisted ball milling can promote the removal of non-cellulose components. The viscosity and modulus of BT-PCNF were relatively higher due to the presence of residual hemicellulose as a natural linker of fibers. The current research provides insights for simplifying the preparation and functionalization of nanocellulose.
In this study, the complexes (FG-P) based on fish gelatin (FG) and pectin (P) were prepared by a simple physical blending within a range of pectin concentrations (0–2%, w/v). The structure, interface, and emulsification properties of the obtained FG-P were analyzed. The binding between FG and pectin was dominated by electrostatic interaction and hydrogen bonding. Introducing pectin substantially increased the viscosity of FG-P. The water contact angle of FG-P gradually decreased with increasing pectin concentration. The highly interfacial viscosity and hydrophilicity of FG-P hindered the interfacial adsorption at the oil/water phase, thereby increasing the interfacial tension and phase angle. This was further manifested as an increase in the viscous modulus and a decrease in both the total modulus and elastic modulus. Despite the inhibition of interfacial adsorption, the unabsorbed FG-P was uniformly dispersed in the continuous phase to form a compact network structure, accompanied with improved rheological properties. Correspondingly, the emulsion precipitation phenomenon was effectively inhibited, and the stability of FG-P stabilized emulsions was improved with decreased droplet size.