通过与 16-hydroxyhexadecanoic acid 和聚(ε-己内酯)混合提高聚(丁二酸丁二醇酯)的海洋生物降解性

IF 6.3 2区 化学 Q1 POLYMER SCIENCE Polymer Degradation and Stability Pub Date : 2024-07-03 DOI:10.1016/j.polymdegradstab.2024.110912
Miwa Suzuki , Shun'ichi Ishii , Minori Ota , Kohei Gonda , Hiroyuki Kashima , Takahiro Arai , Yuya Tachibana , Hiroyuki Takeno , Ken-ichi Kasuya
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引用次数: 0

摘要

减少塑料垃圾对海洋污染的一个潜在解决方案是用可生物降解的替代品取代传统塑料。然而,大多数可化学合成生物降解的脂肪族聚酯,如聚丁二酸丁二醇酯(PBS),在海洋环境中的生物降解速度极慢。为解决这一问题,我们提出了一种新方法,通过将 PBS 与 10 重量百分比的 16-hydroxyhexadecanoic acid(16HHD)和聚(ε-己内酯)(PCL)混合,提高 PBS 在海洋中的生物降解性。含有 16HHD 和 PCL 的 PBS 样品的失重率分别是原始 PBS 的 18.4 倍和 7.8 倍。混合了 16HHD 和 PCL 的 PBS 在海洋中培养四个月后的扫描电子显微照片显示其表面粗糙,表明发生了酶降解。此外,与原始 PBS 不同,在海洋条件下,含有 16HHD 和 PCL 的样品的生化需氧量(BOD)生物降解率分别为 90.4% 和 83.2%。使用 16S 核糖体 RNA 基因测序分析 BOD 测试的微生物群落表明,与原始 PBS 相比,添加 16HHD 和 PCL 改变了微生物群落。这些研究结果表明,在 PBS 中掺入 16HHD 和 PCL 可提高其在海洋中的生物降解性,从而为解决海洋生态系统中的塑料污染问题提供了一种前景广阔的途径。
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Enhancing marine biodegradability of poly(butylene succinate) by blending with 16-hydroxyhexadecanoic acid and poly(ε-caprolactone)

One potential solution for reducing marine pollution from plastic waste is to replace conventional plastics with biodegradable alternatives. However, most chemosynthetically biodegradable aliphatic polyesters, such as poly(butylene succinate) (PBS), exhibit extremely slow biodegradation rates in marine environments. To address this problem, we present a novel method to enhance the marine biodegradability of PBS by blending it with 10 wt.% of 16-hydroxyhexadecanoic acid (16HHD) and poly(ε-caprolactone) (PCL). The weight loss rates of the PBS samples with 16HHD and PCL were 18.4- and 7.8-times faster than that of pristine PBS. Scanning electron micrographs of PBS blended with 16HHD and PCL after oceanic incubation for four months showed a rough surface, suggesting that enzymatic degradation occurred. Additionally, unlike pristine PBS, samples with 16HHD and PCL demonstrated biochemical oxygen demand (BOD) biodegradabilities of 90.4 % and 83.2 %, respectively, under marine conditions. Analysis of the microbial community of BOD testing using 16S ribosomal RNA gene sequencing indicated that the addition of 16HHD and PCL changed the microbial community compared to pristine PBS. These findings demonstrate how blending PBS with 16HHD and PCL enhances its marine biodegradability, thereby offering a promising avenue for addressing plastic pollution in marine ecosystems.

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来源期刊
Polymer Degradation and Stability
Polymer Degradation and Stability 化学-高分子科学
CiteScore
10.10
自引率
10.20%
发文量
325
审稿时长
23 days
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.
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