Alexander R. Craze , Ryan. W. F. Kerr , Thomas M. McGuire , Lukas Wille , Charlotte. K. Williams
{"title":"增韧的商用聚(l-丙交酯)(PLLA)使用可降解和可回收的聚(酯-醚)-b-PLLA†","authors":"Alexander R. Craze , Ryan. W. F. Kerr , Thomas M. McGuire , Lukas Wille , Charlotte. K. Williams","doi":"10.1039/d5gc02301g","DOIUrl":null,"url":null,"abstract":"<div><div>A more sustainable future for plastics relies on the development of high performance materials that are renewably sourced, recycled without suffering losses in performance, and which are, ultimately, degradable to small molecules. Poly(<span>l</span>-lactide) (PLLA) is the largest scale commercial bio-derived plastic, and fulfills many of the above criteria, but is too brittle. Tackling this limitation could allow it to become a substitute for some engineering petrochemical plastics like high impact polystyrene (HIPS) or poly(acrylonitrile-butadiene-styrene) (ABS) which are not recyclable and cannot be easily defossilised. This study focusses on a series of new block polymers as rubber tougheners enabling such PLLA ductility. These block polymers are efficiently synthesised using controlled polymerizations. They are also fully chemically recyclable and biodegradable. The series of new poly(ester-<em>alt</em>-ethers)-<em>b</em>-PLLA show controllable monomer compositions, block ratios and molar mass. They are synthesised using a one-pot switchable catalysis from epoxides, anhydrides and <span>l</span>-lactide, using a well-controlled Zr(<span>iv</span>) catalyst, which selectively forms the poly(ester-<em>alt</em>-ether)-<em>b</em>-PLLA in high yield. The block polymers are blended, using systematically controlled weight percentages, with commercial, semi-crystalline PLLA (<em>M</em><sub>n</sub> = 103 kg mol<sup>−1</sup>, <em>Đ</em> = 1.81). The PLLA blends are comprehensively evaluated using thermal analyses, melt rheology, dynamic mechanical analyses and by tensile mechanical analyses – all techniques show the promise of the new rubber tougheners in improving PLLA properties. The best performing material, featuring 15 wt% block polymer (11 wt% poly(ester-<em>alt</em>-ether)), combines the beneficial high modulus (<em>E</em> = 3.1 ± 0.1 GPa) and high tensile strength (<em>σ</em> = 48.7 ± 1.2 MPa) of PLLA with higher ductility (7× higher than PLLA, <em>ε</em><sub>B</sub> = 24.5 ± 4.6%) and greater tensile toughness (8× PLLA, <em>U</em><sub>T</sub> = 10.8 ± 2.2 MJ m<sup>−3</sup>). Its mechanical properties are improved without compromise to the PLLA thermal properties, as evidenced by very similar glass transition temperature, crystallinity and melt temperature. The PLLA/block polymer blend (15 wt%) shows a lower melt viscosity (3789 Pa s<sup>−1</sup><em>vs.</em> 10 335 Pa s<sup>−1</sup> for PLLA) and earlier onset of shear thinning, facilitating its processing. The PLLA blends are efficiently chemically recycled, using a solid state catalysed process, to <span>l</span>-lactide (87% yield, 100% <span>l</span>-LA selectivity) and the starting poly(ester-<em>alt</em>-ethers)-<em>b</em>-PLLA, facilitating its reuse in blending. The blend components, including the block polymer, are enzymatically degraded, at 37 °C, using <em>Humicola insolens</em> Cutinase over 25 days (HiC, trademark name Novozyme 51032). The properties of these toughened PLLA samples are discussed as replacements for poly(acrylonitrile butadiene styrene) (ABS) and high impact polystyrene (HIPS). In contrast to these petrochemicals, the PLLA blends are bio-derived, fully recyclable and enzymatically degradable after use.</div></div>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":"27 31","pages":"Pages 9495-9511"},"PeriodicalIF":9.2000,"publicationDate":"2025-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Toughened commercial poly(l-lactide) (PLLA) using degradable and recyclable poly(ester-alt-ether)-b-PLLA†\",\"authors\":\"Alexander R. Craze , Ryan. W. F. Kerr , Thomas M. McGuire , Lukas Wille , Charlotte. K. Williams\",\"doi\":\"10.1039/d5gc02301g\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A more sustainable future for plastics relies on the development of high performance materials that are renewably sourced, recycled without suffering losses in performance, and which are, ultimately, degradable to small molecules. Poly(<span>l</span>-lactide) (PLLA) is the largest scale commercial bio-derived plastic, and fulfills many of the above criteria, but is too brittle. Tackling this limitation could allow it to become a substitute for some engineering petrochemical plastics like high impact polystyrene (HIPS) or poly(acrylonitrile-butadiene-styrene) (ABS) which are not recyclable and cannot be easily defossilised. This study focusses on a series of new block polymers as rubber tougheners enabling such PLLA ductility. These block polymers are efficiently synthesised using controlled polymerizations. They are also fully chemically recyclable and biodegradable. The series of new poly(ester-<em>alt</em>-ethers)-<em>b</em>-PLLA show controllable monomer compositions, block ratios and molar mass. They are synthesised using a one-pot switchable catalysis from epoxides, anhydrides and <span>l</span>-lactide, using a well-controlled Zr(<span>iv</span>) catalyst, which selectively forms the poly(ester-<em>alt</em>-ether)-<em>b</em>-PLLA in high yield. The block polymers are blended, using systematically controlled weight percentages, with commercial, semi-crystalline PLLA (<em>M</em><sub>n</sub> = 103 kg mol<sup>−1</sup>, <em>Đ</em> = 1.81). The PLLA blends are comprehensively evaluated using thermal analyses, melt rheology, dynamic mechanical analyses and by tensile mechanical analyses – all techniques show the promise of the new rubber tougheners in improving PLLA properties. The best performing material, featuring 15 wt% block polymer (11 wt% poly(ester-<em>alt</em>-ether)), combines the beneficial high modulus (<em>E</em> = 3.1 ± 0.1 GPa) and high tensile strength (<em>σ</em> = 48.7 ± 1.2 MPa) of PLLA with higher ductility (7× higher than PLLA, <em>ε</em><sub>B</sub> = 24.5 ± 4.6%) and greater tensile toughness (8× PLLA, <em>U</em><sub>T</sub> = 10.8 ± 2.2 MJ m<sup>−3</sup>). Its mechanical properties are improved without compromise to the PLLA thermal properties, as evidenced by very similar glass transition temperature, crystallinity and melt temperature. The PLLA/block polymer blend (15 wt%) shows a lower melt viscosity (3789 Pa s<sup>−1</sup><em>vs.</em> 10 335 Pa s<sup>−1</sup> for PLLA) and earlier onset of shear thinning, facilitating its processing. The PLLA blends are efficiently chemically recycled, using a solid state catalysed process, to <span>l</span>-lactide (87% yield, 100% <span>l</span>-LA selectivity) and the starting poly(ester-<em>alt</em>-ethers)-<em>b</em>-PLLA, facilitating its reuse in blending. The blend components, including the block polymer, are enzymatically degraded, at 37 °C, using <em>Humicola insolens</em> Cutinase over 25 days (HiC, trademark name Novozyme 51032). The properties of these toughened PLLA samples are discussed as replacements for poly(acrylonitrile butadiene styrene) (ABS) and high impact polystyrene (HIPS). In contrast to these petrochemicals, the PLLA blends are bio-derived, fully recyclable and enzymatically degradable after use.</div></div>\",\"PeriodicalId\":78,\"journal\":{\"name\":\"Green Chemistry\",\"volume\":\"27 31\",\"pages\":\"Pages 9495-9511\"},\"PeriodicalIF\":9.2000,\"publicationDate\":\"2025-06-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Green Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1463926225006028\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1463926225006028","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
塑料更可持续的未来依赖于高性能材料的发展,这些材料可再生来源,可回收而不会损失性能,并且最终可降解为小分子。聚l -丙交酯(PLLA)是规模最大的商业生物衍生塑料,满足上述许多标准,但太脆。解决这一限制可以使它成为一些工程石化塑料的替代品,如高冲击聚苯乙烯(HIPS)或聚丙烯腈-丁二烯-苯乙烯(ABS),这些塑料不可回收,也不易分解。本研究的重点是一系列新的嵌段聚合物作为橡胶增韧剂,使pla具有这样的延展性。这些嵌段聚合物是通过控制聚合有效地合成的。它们也是完全化学可回收和可生物降解的。该系列新型聚(酯-alt-醚)-b-PLLA单体组成、嵌段比和摩尔质量可控。它们是用一锅可切换的催化剂合成的,由环氧化物、酸酐和l-丙交酯,使用控制良好的Zr(IV)催化剂,选择性地形成高收率的聚(酯-醚)-b-PLLA。用系统控制的重量百分比将嵌段聚合物与商业半结晶PLLA (Mn = 103 kg mol - 1, Đ = 1.81)混合。使用热分析、熔体流变学、动态力学分析和拉伸力学分析对PLLA共混物进行了全面评估-所有技术都显示了新型橡胶增韧剂在改善PLLA性能方面的前景。性能最佳的材料为15 wt%嵌段聚合物(11 wt%聚(酯-醚)),具有PLLA的高模量(E = 3.1±0.1 GPa)和高抗拉强度(σ = 48.7±1.2 MPa)、高延展性(比PLLA高7倍,εB = 24.5±4.6%)和高拉伸韧性(8× PLLA, UT = 10.8±2.2 MJ m−3)。在不影响PLLA热性能的情况下,它的机械性能得到了改善,这一点可以从非常相似的玻璃化转变温度、结晶度和熔体温度中得到证明。PLLA/嵌段聚合物共混物(15 wt%)的熔体粘度较低(3789 Pa s−1vs)。10 335 Pa s−1 (PLLA))和更早的剪切变薄,有利于其加工。PLLA共混物通过固态催化过程有效地进行化学回收,生成l -丙交酯(产率87%,L-LA选择性100%)和起始聚(酯-醚)-b-PLLA,便于其在共混中重复使用。在37°C下,使用Humicola insolens角质酶(HiC,商标名Novozyme 51032)酶降解共混组分,包括块状聚合物。讨论了这些增韧PLLA样品作为聚丙烯腈丁二烯苯乙烯(ABS)和高冲击聚苯乙烯(HIPS)的替代品的性能。与这些石化产品相比,pla共混物是生物衍生的,完全可回收,使用后可酶降解。
Toughened commercial poly(l-lactide) (PLLA) using degradable and recyclable poly(ester-alt-ether)-b-PLLA†
A more sustainable future for plastics relies on the development of high performance materials that are renewably sourced, recycled without suffering losses in performance, and which are, ultimately, degradable to small molecules. Poly(l-lactide) (PLLA) is the largest scale commercial bio-derived plastic, and fulfills many of the above criteria, but is too brittle. Tackling this limitation could allow it to become a substitute for some engineering petrochemical plastics like high impact polystyrene (HIPS) or poly(acrylonitrile-butadiene-styrene) (ABS) which are not recyclable and cannot be easily defossilised. This study focusses on a series of new block polymers as rubber tougheners enabling such PLLA ductility. These block polymers are efficiently synthesised using controlled polymerizations. They are also fully chemically recyclable and biodegradable. The series of new poly(ester-alt-ethers)-b-PLLA show controllable monomer compositions, block ratios and molar mass. They are synthesised using a one-pot switchable catalysis from epoxides, anhydrides and l-lactide, using a well-controlled Zr(iv) catalyst, which selectively forms the poly(ester-alt-ether)-b-PLLA in high yield. The block polymers are blended, using systematically controlled weight percentages, with commercial, semi-crystalline PLLA (Mn = 103 kg mol−1, Đ = 1.81). The PLLA blends are comprehensively evaluated using thermal analyses, melt rheology, dynamic mechanical analyses and by tensile mechanical analyses – all techniques show the promise of the new rubber tougheners in improving PLLA properties. The best performing material, featuring 15 wt% block polymer (11 wt% poly(ester-alt-ether)), combines the beneficial high modulus (E = 3.1 ± 0.1 GPa) and high tensile strength (σ = 48.7 ± 1.2 MPa) of PLLA with higher ductility (7× higher than PLLA, εB = 24.5 ± 4.6%) and greater tensile toughness (8× PLLA, UT = 10.8 ± 2.2 MJ m−3). Its mechanical properties are improved without compromise to the PLLA thermal properties, as evidenced by very similar glass transition temperature, crystallinity and melt temperature. The PLLA/block polymer blend (15 wt%) shows a lower melt viscosity (3789 Pa s−1vs. 10 335 Pa s−1 for PLLA) and earlier onset of shear thinning, facilitating its processing. The PLLA blends are efficiently chemically recycled, using a solid state catalysed process, to l-lactide (87% yield, 100% l-LA selectivity) and the starting poly(ester-alt-ethers)-b-PLLA, facilitating its reuse in blending. The blend components, including the block polymer, are enzymatically degraded, at 37 °C, using Humicola insolens Cutinase over 25 days (HiC, trademark name Novozyme 51032). The properties of these toughened PLLA samples are discussed as replacements for poly(acrylonitrile butadiene styrene) (ABS) and high impact polystyrene (HIPS). In contrast to these petrochemicals, the PLLA blends are bio-derived, fully recyclable and enzymatically degradable after use.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.