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Transitions seen in the electric properties of water-absorbable poly(2,5-benzimidazole) (ABPBI) films were confirmed by electric conductivity, dielectric constant, and time-domain nuclear magnetic resonance (NMR) measurements. The electric resistance of the films was measured at room temperature using a high-resistance meter, and the dielectric constant at room temperature was measured using an LCR meter in the frequency range of 90 Hz to 8 MHz. The water absorption ratio at equilibrium absorption for the films was 37%, which corresponded to a volume fraction of water of 0.33. The electric conductivity of the films without water absorption was ~1014 S·cm−1, and it increased to ~1010 S·cm−1 with increasing volume fraction, showing a percolation threshold at a volume fraction of 0.025, and remarkable transitions at volume fractions of 0.075 and 0.135. The dielectric constant of the films without water absorption was 3.4, and it increased to 8.1 with increasing volume fraction, showing a transition only at a volume fraction of 0.135. Above a volume fraction of 0.075, where a transition in conductivity was observed, there were two relaxation times at 18–31 μs and 20–93 μs, as determined from the time-domain NMR, and these relaxation times increased with increasing volume fraction. The longer relaxation time increased significantly at a volume fraction of 0.072, which was close to the volume fraction of the transition seen in conductivity. The relationship between the chain mobility of ABPBI and the deterioration in electric insulating properties is discussed. [ABSTRACT FROM AUTHOR]

Polybenzimidazole (PBI) is a high-performance polymer known for its excellent thermal stability, mechanical strength, and chemical resistance, attributes that are derived from its unique structure comprising repeated benzene and imidazole rings. However, limitations such as relatively low thermal stability and moisture sensitivity restrict its application as a super engineering plastic. In this study, amide groups are incorporated into the PBI backbone to synthesize the copolymer poly(BI-co-A), effecting a structural modification at the molecular level. Additionally, silica nanospheres were composited into the poly(BI-co-A) film to further enhance its thermal performance. The resulting composite films exhibited remarkable thermal stability, with the temperature for 10% weight loss reaching as high as 761 °C. To address increased water absorption due to the high hydrophilicity of hydroxyl groups on the silica nanospheres' surface, a dehydration treatment was applied in an electric furnace. This treatment produced a highly thermoresistant poly(BI-co-A) nanocomposite film with reduced wettability, making it suitable for applications in humid environments. [ABSTRACT FROM AUTHOR]

High-molecular-weight polypeptides with functional aromatic side chains, poly(4-amino-l-phenylalanine), were prepared by the metal-initiated polymerization of the Nα-carboxyanhydride of the corresponding amino acid, which is a microbial derivative of phenylalanine.

Polyamides (PAs) with aspartame‐derived diketopiperazine (DKP) form specific particles and exhibit high heat resistance. In this study, we investigated the stereostructures of aspartic acid and phenylalanine, which constitute aspartame DKP. Diketopiperazines with different stereostructures were synthesized from D‐ and L‐aspartic acid and D‐ and L‐phenylalanine, and LL‐, DD‐, and LD‐type aminodiketopiperazines (LL, DD, and LD‐ADKPs) were obtained. These ADKPs differed in their crystal forms depending on their stereoisomeric structures. Furthermore, PAs were formed from these ADKPs via polycondensation using triphenyl phosphite/pyridine, and their heat resistance was approximately 300 °C. The secondary structure of each PA was evaluated by circular dichroism, which suggested that LD‐type PAs had a mixed secondary structure of coils and helical structures, unlike the LL and DD types. Precipitated LL, DD, and LLcoDD PAs formed similar particles, whereas the particles of the large LD‐type PA had different particle shapes owing to their different conformations. [ABSTRACT FROM AUTHOR]

Composite xerogel films with structural orientation, controlled swelling degree, and drug‐release ability are prepared using biocompatible megamolecular liquid crystalline polysaccharide (sacran) secreted by a cyanobacterium Aphanothece sacrum. The sacran xerogel films (Sac‐XFs) are formed by drying sacran aqueous solution including vitamin C (L‐ascorbic acid, AA) and trehalose under various conditions. In X‐ray diffraction and differential scanning calorimetry of Sac‐XFs, diffractions or melting points of either AA or trehalose are not detected, indicating no crystal formation. Additionally, the stability of entrapped AA in Sac‐XFs is evaluated through changes in film color and percentage loss, to indicate that AA stability is enhanced by entrapment in Sac‐XFs in the presence of trehalose. Scanning electron microscopy of Sac‐XFs reveals the morphological orientation, and number of striped lines along the longitudinal axis of film edges on side views while no visible textures in top views. When Sac‐XFs are immersed in water, anisotropic swelling is observed, and anisotropy decreases with an increase in the drying temperature of the films. AA is released preferentially from the hydrogel sheet edges, indicating the direction‐controlled release. Thus, the trehalose/sacran composite xerogels offer an alternative platform for preserving and controlled‐releasing sensitive substances for fields of foods, pharmaceutics, and cosmetics. [ABSTRACT FROM AUTHOR]

Tunable hydrogels have gained significant attention in the bioengineering field due to their designer preparation approach. Towards this end, gelatine stands out as a promising candidate owing to its desirable attributes, such as biocompatibility, ability to support cell adhesion and proliferation, biodegradability, and cost-effectiveness. This study presents the preparation of a robust gelatine hydrogel employing sacran aldehyde (SDA) as a natural cross-linker. The resulting SDA-cross-linked gelatine hydrogels (GSDA) display an optimal compressive stress of 0.15 MPa at 50% strain, five times higher than pure gelatine hydrogel. As SDA cross-linking concentration is increased, the swelling capacity of GSDA declines. This decline in swelling capacity, from 80% to 40%, is a result of strong crosslinking of gelatin with SDA. Probing further with FT-IR spectroscopy and SEM at the micron scale unveiled a dual-cross-linking mechanism within the hydrogels. This mechanism encompasses both short- and long-range covalent cross-linking, along with thermo-induced physical cross-linking, resulting in a significant enhancement of the load-bearing capacity of the fabricated hydrogels. [ABSTRACT FROM AUTHOR]