Kwang-Hyun Ryu , Ji-Hyun Cho , Hoon Kim , Hyeon-Su Jo , Jong-Ho Back , Hyun-Joong Kim
{"title":"为可持续热熔胶设计可生物降解共聚聚酯的规则性:粘附性、可移除性和生物降解性","authors":"Kwang-Hyun Ryu , Ji-Hyun Cho , Hoon Kim , Hyeon-Su Jo , Jong-Ho Back , Hyun-Joong Kim","doi":"10.1016/j.polymdegradstab.2024.111022","DOIUrl":null,"url":null,"abstract":"<div><div>Recent research has increased in eco-friendly hot-melt adhesives as alternatives to conventional commercial hot-melt adhesives. However, there have been limitations in terms of removability and biodegradability. This study addresses these issues by designing a novel molecular structure for a single polymer, resulting in a sustainable hot-melt adhesive that offers strong adhesion, clear removability, and high biodegradability without additional additives. By varying the ratio of alcohol monomers 1,4-butanediol (BD) and ethylene glycol (EG) during polymerization, we synthesized poly(butylene adipate-co-butylene terephthalate-co-ethylene adipate-co-ethylene terephthalate) (PBEAT) with four block segments. We increased the open time by reducing the regularity of the molecular structure, controlling crystallization behavior, and inhibiting polymer chain packing. This improvement in wettability with the adherend allowed us to achieve a lap shear adhesion strength of 3.18 MPa. Additionally, we proposed a debonding mechanism based on the correlation between the crystallization temperature (T<sub>c</sub>) block copolymer's and shear adhesion failure temperature (SAFT), demonstrating the removability of the prepared hot-melt adhesive. Finally, analyses of hydrolysis, enzymatic degradation, and biodegradation in compost confirmed that reduced crystallinity enhances biodegradability. PBE<sub>30</sub>AT, exhibiting the strongest adhesion strength, achieves complete degradation in compost within 20 days, faster than neat poly(butylene adipate-co-terephthalate) (PBAT). This research offers a novel and practical approach to enhancing the potential and expandability of sustainable adhesives by tailoring the molecular structure of the polymer.</div></div>","PeriodicalId":406,"journal":{"name":"Polymer Degradation and Stability","volume":"230 ","pages":"Article 111022"},"PeriodicalIF":6.3000,"publicationDate":"2024-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Designing the regularity of biodegradable copolyester for sustainable hot-melt adhesives: Adhesion, removability, and biodegradability\",\"authors\":\"Kwang-Hyun Ryu , Ji-Hyun Cho , Hoon Kim , Hyeon-Su Jo , Jong-Ho Back , Hyun-Joong Kim\",\"doi\":\"10.1016/j.polymdegradstab.2024.111022\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Recent research has increased in eco-friendly hot-melt adhesives as alternatives to conventional commercial hot-melt adhesives. However, there have been limitations in terms of removability and biodegradability. This study addresses these issues by designing a novel molecular structure for a single polymer, resulting in a sustainable hot-melt adhesive that offers strong adhesion, clear removability, and high biodegradability without additional additives. By varying the ratio of alcohol monomers 1,4-butanediol (BD) and ethylene glycol (EG) during polymerization, we synthesized poly(butylene adipate-co-butylene terephthalate-co-ethylene adipate-co-ethylene terephthalate) (PBEAT) with four block segments. We increased the open time by reducing the regularity of the molecular structure, controlling crystallization behavior, and inhibiting polymer chain packing. This improvement in wettability with the adherend allowed us to achieve a lap shear adhesion strength of 3.18 MPa. Additionally, we proposed a debonding mechanism based on the correlation between the crystallization temperature (T<sub>c</sub>) block copolymer's and shear adhesion failure temperature (SAFT), demonstrating the removability of the prepared hot-melt adhesive. Finally, analyses of hydrolysis, enzymatic degradation, and biodegradation in compost confirmed that reduced crystallinity enhances biodegradability. PBE<sub>30</sub>AT, exhibiting the strongest adhesion strength, achieves complete degradation in compost within 20 days, faster than neat poly(butylene adipate-co-terephthalate) (PBAT). This research offers a novel and practical approach to enhancing the potential and expandability of sustainable adhesives by tailoring the molecular structure of the polymer.</div></div>\",\"PeriodicalId\":406,\"journal\":{\"name\":\"Polymer Degradation and Stability\",\"volume\":\"230 \",\"pages\":\"Article 111022\"},\"PeriodicalIF\":6.3000,\"publicationDate\":\"2024-10-03\",\"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/S0141391024003665\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Degradation and Stability","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0141391024003665","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Designing the regularity of biodegradable copolyester for sustainable hot-melt adhesives: Adhesion, removability, and biodegradability
Recent research has increased in eco-friendly hot-melt adhesives as alternatives to conventional commercial hot-melt adhesives. However, there have been limitations in terms of removability and biodegradability. This study addresses these issues by designing a novel molecular structure for a single polymer, resulting in a sustainable hot-melt adhesive that offers strong adhesion, clear removability, and high biodegradability without additional additives. By varying the ratio of alcohol monomers 1,4-butanediol (BD) and ethylene glycol (EG) during polymerization, we synthesized poly(butylene adipate-co-butylene terephthalate-co-ethylene adipate-co-ethylene terephthalate) (PBEAT) with four block segments. We increased the open time by reducing the regularity of the molecular structure, controlling crystallization behavior, and inhibiting polymer chain packing. This improvement in wettability with the adherend allowed us to achieve a lap shear adhesion strength of 3.18 MPa. Additionally, we proposed a debonding mechanism based on the correlation between the crystallization temperature (Tc) block copolymer's and shear adhesion failure temperature (SAFT), demonstrating the removability of the prepared hot-melt adhesive. Finally, analyses of hydrolysis, enzymatic degradation, and biodegradation in compost confirmed that reduced crystallinity enhances biodegradability. PBE30AT, exhibiting the strongest adhesion strength, achieves complete degradation in compost within 20 days, faster than neat poly(butylene adipate-co-terephthalate) (PBAT). This research offers a novel and practical approach to enhancing the potential and expandability of sustainable adhesives by tailoring the molecular structure of the polymer.
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.