Chitosan-Coated Bacterial Cellulose (BC)/Hydrolyzed Collagen Films and Their Ascorbic Acid Loading/Releasing Performance: A Utilization of BC Waste from Kombucha Tea Fermentation.

SCOBY bacterial cellulose (BC) is a biological macromolecule (considered as a by-product) that grows at the liquid-air interface during kombucha tea fermentation. In this study, BC:HC (hydrolyzed collagen) blend films coated with 1 wt% chitosan (CS) were loaded with ascorbic acid to study loading/releasing performance. At first, the mechanical properties of the blend films were found to be dependent on HC ratio. After chitosan coating, the coated films were stronger due to intermolecular hydrogen bonding interaction and the miscibility of two matrixes at the interface. The antibacterial activity test according to the AATCC Test Method revealed that chitosan-coated BC/HC films exhibited excellent antimicrobial activity against S.aureus growth from the underneath and the above film when compared to BC and BC:HC films. Moreover, chitosan was attractive to ascorbic acid during drug loading. Consequently, its releasing performance was very poor. For BC:HC blend films, ascorbic acid loading/releasing performance was balanced by water swellability, which was controlled using blending formulation and coating. Another advantage of BC films and BC:HC blend films was that they were able to maintain active ascorbic acid for a long period of time, probably due to the presence of plenty of BC hemiacetal reducing ends (protective group).

Multilayered bacterial cellulose/reduced graphene oxide composite films for self-standing and binder-free electrode application.

Multilayered bacterial cellulose (MBC)/reduced graphene oxide (rGO) composite films were fabricated using dyeing method. First, MBC films were constructed by the static culturing of kombucha SCOBY bacterial cellulose in a rectangular plastic mold for 15 days. The MBC formed on the air-liquid interface was collected and employed as the matrix for the preparation of MBC/rGO composite films using dyeing method. As found, the color strength increased with an increase in dyeing cycle due to MBC and GO (rGO precursor) affinity. However, the surface hydrophilicity was found in the opposite direction due to the restacking of hydrophobic rGO nanosheets onto MBC surface after reduction step. SEM images confirmed that MBC/rGO composite films obtained by the dyeing method exhibited the intact multilayer structure. The electrochemical behavior of free-standing and binder-free MBC/rGO electrodes was evaluated. It was found that MBC-1 exhibited the highest specific capacitance value of 192.23 F/g at the current density of 1 A/g (calculated from GCD plots) due to good diffusion of electrolyte arising from surface wettability with current density performance of 66 %. An increase in dyeing cycle (MBC-2, MBC-3, and MBC-4) led to a gradual decrease in the corresponding specific capacitance value due to a gradual increase in the electrolyte resistance derived from an increasing surface hydrophobicity of the composite films. Finally, in all cases, long-term cycle stability of more than 90 % up to 10000 cycles was achievable.

Preparation and Characterizations of PSS/PDADMAC Polyelectrolyte Complex Hydrogel.

Polyelectrolyte complex (PEC) hydrogel, formed via physically electrostatic crosslinks between polyanion and polycation, is an interesting hydrogel in terms of its nontoxicity and solvent-free technique. In this work, poly (sodium 4-styrenesulfonate) (PSS)/poly (diallyl dimethyl ammonium chloride) (PDADMAC) complex hydrogels were prepared. Firstly, the PSS/PDADMAC complex aggregates using various PSS/PDADMAC mole fractions that were prepared in the presence of NaCl solution. Then, the aggregates were resolubilized under stirring at 70 °C for 2 h to obtain a homogeneous PEC solution. Finally, the PEC solution was dialyzed using a dialysis membrane with 3500 molecular cut-off for 1 day. The dialysis bath was changed every interval period of 2 h to control the rate of reversible electrostatic interaction, resulting in the homogenous PEC hydrogel with porous morphology as revealed by SEM and BET investigations. The dimensional stability and viscoelasticity of the PEC hydrogel was studied by DMA experiment, which showed the viscoelastic behavior at a compressive force ranging from 0 to 0.1 N. Finally, PSS/PDADMAC hydrogels showed a high water absorbency property and excellent affinity to textile anionic dyes.

Poly(lactic acid) filled with cassava starch-g-soybean oil maleate.

Poly(lactic acid), PLA, is a biodegradable polymer, but its applications are limited by its high cost and relatively poorer properties when compared to petroleum-based plastics. The addition of starch powder into PLA is one of the most promising efforts because starch is an abundant and cheap biopolymer. However, the challenge is the major problem associated with poor interfacial adhesion between the hydrophilic starch granules and the hydrophobic PLA, leading to poorer mechanical properties. In this paper, soybean oil maleate (SOMA) was synthesized by grafting soybean oil with various weight percents of maleic anhydride (MA) using dicumyl peroxide (DCP) as an initiator. Then, SOMA was employed for the surface modifying of cassava starch powder, resulting in SOMA-g-STARCH. The obtained SOMA-g-STARCH was mixed with PLA in various weight ratios using twin-screw extruder, resulting in PLA/SOMA-g-STARCH. Finally, the obtained PLA/SOMA-g-STARCH composites were prepared by a compression molding machines. The compatibility, thermal properties, morphology properties, and mechanical properties were characterized and evaluated. The results showed that the compatibility, surface appearance, and mechanical properties at 90 : 10 and 80 : 20 ratios of PLA/SOMA-g-STARCH were the best.