Hanjiao Zhang , Haojia Chen , Tiexian Liang , Dehua Wen , Xin Chen , Xiaotu Liu , Yan Yang , Hongbing Ji
{"title":"Microbial degradation behavior and mechanism of polyamide 6 fibers in seawater","authors":"Hanjiao Zhang , Haojia Chen , Tiexian Liang , Dehua Wen , Xin Chen , Xiaotu Liu , Yan Yang , Hongbing Ji","doi":"10.1016/j.polymdegradstab.2025.111676","DOIUrl":null,"url":null,"abstract":"<div><div>Polyamide 6 (PA6) is a widely used thermoplastic polymer. Compared to other nylons, it offers good mechanical properties as well as chemical and thermal stability. Difficult to degrade and coupled with its massive annual global production, it has rapidly become a significant ecological pollutant. Therefore, developing environmentally friendly degradation methods is an urgent need, among which microbial degradation represents a promising solution. This study conducted laboratory-simulated seawater degradation experiments on polyamide 6 (PA6) fibers. The structural changes of PA6 over a 190-day degradation period were analyzed using characterization techniques, including scanning electron microscopy, relative viscosity, and differential scanning calorimetry. Results demonstrated significant and irregular degradation of PA6. Prolonged degradation led to decreases in relative viscosity, number-average molecular weight, melting temperature, and melting enthalpy. FTIR and XPS analyses revealed cleavage of C–C, C–N, and <em>C</em> = <em>O</em> bonds, accompanied by intensified signals of C–OH and <em>O</em> = <em>C</em>–O–C groups, indicating hydrolysis of amide bonds to generate terminal amino and carboxyl groups. Degradation product analysis suggested that the initial step of PA6 degradation primarily produced tetrameric and cyclic dimeric forms of 6-aminohexanoic acid. Further microbial community analysis and functional annotation identified <em>Proteobacteria</em> as the dominant microbial population responsible for PA6 degradation. This study provides new insights into the degradation behavior of polyamide fibers in marine environments and contributes substantially to solving the problem of marine polyamide waste.</div></div>","PeriodicalId":406,"journal":{"name":"Polymer Degradation and Stability","volume":"242 ","pages":"Article 111676"},"PeriodicalIF":7.4000,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Degradation and Stability","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0141391025005051","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Polyamide 6 (PA6) is a widely used thermoplastic polymer. Compared to other nylons, it offers good mechanical properties as well as chemical and thermal stability. Difficult to degrade and coupled with its massive annual global production, it has rapidly become a significant ecological pollutant. Therefore, developing environmentally friendly degradation methods is an urgent need, among which microbial degradation represents a promising solution. This study conducted laboratory-simulated seawater degradation experiments on polyamide 6 (PA6) fibers. The structural changes of PA6 over a 190-day degradation period were analyzed using characterization techniques, including scanning electron microscopy, relative viscosity, and differential scanning calorimetry. Results demonstrated significant and irregular degradation of PA6. Prolonged degradation led to decreases in relative viscosity, number-average molecular weight, melting temperature, and melting enthalpy. FTIR and XPS analyses revealed cleavage of C–C, C–N, and C = O bonds, accompanied by intensified signals of C–OH and O = C–O–C groups, indicating hydrolysis of amide bonds to generate terminal amino and carboxyl groups. Degradation product analysis suggested that the initial step of PA6 degradation primarily produced tetrameric and cyclic dimeric forms of 6-aminohexanoic acid. Further microbial community analysis and functional annotation identified Proteobacteria as the dominant microbial population responsible for PA6 degradation. This study provides new insights into the degradation behavior of polyamide fibers in marine environments and contributes substantially to solving the problem of marine polyamide waste.
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.