Chaochen Xu , Weicheng Yang , Shaojie Shi , Wufeng Shen , Chao Zeng , Shengming Zhang , Peng Ji , Chaosheng Wang , Huaping Wang
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引用次数: 0
Abstract
The development of degradable plastics is crucial for addressing the issue of plastic pollution. Although poly(butylene adipate terephthalate) (PBAT) is a degradable polyester, it has stringent environmental requirements for degradation and necessitates urgent modification. Triethanolamine (TEOA), an inexpensive industrial product, was introduced into the molecular chain of PBAT to facilitate branching and enhance catalytic synergy. poly(butylene adipate terephthalate - triethanolamine) (PBAT-TEOA) with TEOA contents ranging from 0.25% to 4% were synthesized. The results indicate that the introduction of triethanolamine significantly shortens the polycondensation time while maintaining favorable coloration (b value < 10). Additionally, the mechanical properties of the copolyester can be slightly improved with minimal TEOA incorporation. Specifically, PBAT-TEOA0.5 exhibits a tensile strength of 20.96 MPa. However, this strength declines rapidly when TEOA content exceeds 1%. Furthermore, TEOA enhances both the hydrophilicity and enzymatic as well as hydrolytic properties of the copolyester. Notably, PBAT-TEOA0.25 underwent hydrolysis in PBS buffer over a period of 49 days, resulting in a mass residual rate of 89.86%. The branched structure can be disrupted through the Cope elimination reaction, thereby accelerating degradation following treatment with hydrogen peroxide (H2O2). The number average molecular weight of PBAT-TEOA2 decreases by 35.53% after the oxidative treatment. Finally, melt spinning was conducted on PBAT-TEOAs to prepare degradable polyester fibers with a fiber strength of 1.98 cN/dtex. This work presents a straightforward, efficient and cost-effective strategy for enhancing both the degradation performance and spinnability of PBAT with good coloration.
期刊介绍:
Polymer Degradation and Stability deals with the degradation reactions and their control which are a major preoccupation of practitioners of the many and diverse aspects of modern polymer technology.
Deteriorative reactions occur during processing, when polymers are subjected to heat, oxygen and mechanical stress, and during the useful life of the materials when oxygen and sunlight are the most important degradative agencies. In more specialised applications, degradation may be induced by high energy radiation, ozone, atmospheric pollutants, mechanical stress, biological action, hydrolysis and many other influences. The mechanisms of these reactions and stabilisation processes must be understood if the technology and application of polymers are to continue to advance. The reporting of investigations of this kind is therefore a major function of this journal.
However there are also new developments in polymer technology in which degradation processes find positive applications. For example, photodegradable plastics are now available, the recycling of polymeric products will become increasingly important, degradation and combustion studies are involved in the definition of the fire hazards which are associated with polymeric materials and the microelectronics industry is vitally dependent upon polymer degradation in the manufacture of its circuitry. Polymer properties may also be improved by processes like curing and grafting, the chemistry of which can be closely related to that which causes physical deterioration in other circumstances.