Jilei Han, Zhe Wang, Yuxuan Yang, Dan Liu, Chunmei Niu, Ruolin Wang
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引用次数: 0
Abstract
Aiming at the main application bottlenecks of long degradation cycle and poor antibacterial property of disposable carboxylated nitrile butadiene rubber (XNBR) gloves, APS-iron (APS-Fe) chelate was employed as a multifunctional modifier to prepare XNBR/APS-Fe composite films through compounding and vulcanization processes. Utilizing APS-Fe's dual properties (metal-catalyzed aging and biodegradability), we established a “catalysis-biology” dual-driven rapid degradation system. The service life of the XNBR/1.5APS-Fe composite film to reach the 75% threshold of fracture retention at 25 °C was only 4.34 years, significantly shorter than its natural degradation cycle. With the synergistic effect of the active groups of APS and Fe3+, the composite film exhibited remarkably enhanced scavenging capacity for hydroxyl radicals and DPPH radicals, effectively addressing the shortcoming of weak antibacterial property of pure XNBR. The antibacterial capacity of XNBR/1.5APS-Fe against Escherichia coli was prominent, 11.4 times higher than that of pure XNBR. Additionally, the mechanical properties and solvent resistance of XNBR films were also improved. The novel composite film combines excellent properties such as degradability, antioxidant activity, and antibacterial safety. These findings provide a scientific and practical solution for the development of functional disposable rubber products.
期刊介绍:
Composites Science and Technology publishes refereed original articles on the fundamental and applied science of engineering composites. The focus of this journal is on polymeric matrix composites with reinforcements/fillers ranging from nano- to macro-scale. CSTE encourages manuscripts reporting unique, innovative contributions to the physics, chemistry, materials science and applied mechanics aspects of advanced composites.
Besides traditional fiber reinforced composites, novel composites with significant potential for engineering applications are encouraged.