纤维素
极限抗拉强度
化学工程
生物降解
材料科学
接触角
吸附
催化作用
硅氧烷
点击化学
氢键
生物相容性
生物高聚物
高分子化学
有机化学
化学
复合材料
分子
聚合物
工程类
作者
Haiqin Liu,Bowen Li,Sijie Gong,Haiyang Ding,Yimin Fan,Juan Yu
标识
DOI:10.1016/j.ijbiomac.2024.131008
摘要
The construction of functional cellulose plastics possessing strong UV-blocking, hydrophilicity, and biodegradability is challenging. Therefore, we provide a novel strategy to successfully prepare sustainable and hydrophilic glucose-cross-linked cellulose (GC) plastics showing effective UV-blocking and excellent mechanical properties via hydroxyl-yne click reaction at room temperature. The results demonstrated that hydroxyl-yne click chemistry enabled efficient crosslinking of cellulose with glucose using 4-dimethylamino pyridine (DMAP) as a catalyst. Moreover, the DMAP residue imparted good UV-shielding properties to GC films exhibiting nearly 100 % UVC (200–275 nm) and 100 % UVB (320–275 nm) shielding ratios. The introduction of glucose imparted superior hydrophilicity (water contact angle of 40.3–43.2°) and improved water adsorption. Additionally, the mechanical properties of the GC films increased with the increasing crosslinking density, and the highest tensile stress was 94 MPa. The water-induced breaking and hydrogen bond reforming strategy led to a stress of 127 MPa and a strain of 25.6 % for the final GC2 film, which were excellent compared to those of the most reported cellulose films. Additionally, GC films were biosafe, exhibited improved oxygen barrier, and good biodegradability. Hence, this study provides a promising and efficient approach for preparing high-performance cellulose plastics.
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