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从传统增塑剂向通过乙酰丙酸和甘油增值获得的多功能生物增塑剂转变的进一步进展。

Further Step in the Transition from Conventional Plasticizers to Versatile Bioplasticizers Obtained by the Valorization of Levulinic Acid and Glycerol.

作者信息

Lenzi Luca, Degli Esposti Micaela, Braccini Simona, Siracusa Chiara, Quartinello Felice, Guebitz Georg M, Puppi Dario, Morselli Davide, Fabbri Paola

机构信息

Department of Civil, Chemical, Environmental, and Materials Engineering (DICAM), Università di Bologna, Via U. Terracini 28, 40131 Bologna, Italy.

National Interuniversity Consortium of Materials Science and Technology (INSTM), Via G. Giusti 9, 50121 Firenze, Italy.

出版信息

ACS Sustain Chem Eng. 2023 Jun 13;11(25):9455-9469. doi: 10.1021/acssuschemeng.3c01536. eCollection 2023 Jun 26.

Abstract

In the last two decades, the use of phthalates has been restricted worldwide due to their well-known toxicity. Nonetheless, phthalates are still widely used for their versatility, high plasticization effect, low cost, and lack of valuable alternatives. This study presents the fully bio-based and versatile glycerol trilevulinate plasticizer (GT) that was obtained by the valorization of glycerol and levulinic acid. The mild-conditions and solvent-free esterification used to synthesize GT was optimized by investigating the product by Fourier transform infrared and NMR spectroscopy. An increasing content of GT, from 10 to 40 parts by weight per hundred parts of resin (phr), was tested with poly(vinyl chloride), poly(3-hydroxybutyrate), poly(3-hydroxybutyrate--3-hydroxyvalerate), poly(lactic acid), and poly(caprolactone), which typically present complicated processability and/or mechanical properties. GT produced a significant plasticization effect on both amorphous and semicrystalline polymers, reducing their glass-transition temperature and stiffness, as observed by differential scanning calorimetry measurements and tensile tests. Remarkably, GT also decreased both the melting temperature and crystallinity degree of semicrystalline polymers. Furthermore, GT underwent enzyme-mediated hydrolysis to its initial constituents, envisioning a promising prospective for environmental safety and upcycling. Furthermore, 50% inhibitory concentration (IC) tests, using mouse embryo fibroblasts, proved that GT is an unharmful alternative plasticizer, which makes it potentially applicable in the biomedical field.

摘要

在过去二十年中,由于邻苯二甲酸盐众所周知的毒性,其在全球范围内的使用受到了限制。尽管如此,由于其多功能性、高增塑效果、低成本以及缺乏有价值的替代品,邻苯二甲酸盐仍被广泛使用。本研究展示了一种完全基于生物的多功能甘油三乙酰丙酸酯增塑剂(GT),它是通过甘油和乙酰丙酸的增值转化而获得的。通过傅里叶变换红外光谱和核磁共振光谱对产物进行研究,优化了用于合成GT的温和条件和无溶剂酯化反应。用聚氯乙烯、聚(3-羟基丁酸酯)、聚(3-羟基丁酸酯-3-羟基戊酸酯)、聚乳酸和聚己内酯测试了GT的含量增加情况,从每百份树脂10至40重量份(phr),这些聚合物通常具有复杂的加工性能和/或机械性能。通过差示扫描量热法测量和拉伸试验观察到,GT对无定形和半结晶聚合物均产生了显著的增塑效果,降低了它们的玻璃化转变温度和硬度。值得注意的是,GT还降低了半结晶聚合物的熔点和结晶度。此外,GT可通过酶介导水解为其初始成分,这为环境安全和升级回收带来了有前景的展望。此外,使用小鼠胚胎成纤维细胞进行的50%抑制浓度(IC)测试证明,GT是一种无害的替代增塑剂,这使其有可能应用于生物医学领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/773e/10302884/a3c2dd2acd96/sc3c01536_0008.jpg

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