Osório Brandão João Augusto, Morisso Fernando Dal Pont, Francisquetti Edson Luiz, Campomanes Santana Ruth Marlene
Federal University of Rio Grande do Sul (UFRGS), Engineering School, Laboratory of Polymeric Materials (LAPOL), Bento Gonçalves Ave, 9500, 91501-970, Porto Alegre, Brazil.
Feevale Universtiy, Laboratory for Advanced Materials Studies, ERS-239, 2755, 93525-075, Novo Hamburgo, Brazil.
Heliyon. 2022 Aug 13;8(8):e10217. doi: 10.1016/j.heliyon.2022.e10217. eCollection 2022 Aug.
In an attempt to reduce the accumulation of polymeric waste in the environment, such as plastic bags, the use of pro-oxidants has been adopted in polyolefins, including polyethylene (PE), which is one of the most used polymers in film production. The incorporation of this additive to PE film aims to accelerate its oxidation in the process of abiotic degradation, generating oxygenated groups that can facilitate the biotic degradation. Commercial pro-oxidants are commonly organic salts of transition metals. However, their use can lead to a secondary problem, the inappropriate accumulation of transition metals at the site where the polymeric waste was deposited and, for this reason, it has been sought pro-oxidants metals free and that can also be biodegraded. In this context, this work aimed to evaluate the photodegradation of PE blown films obtained by extrusion using a commercial pro-oxidant, d2w™, an alternative organic pro-oxidant, benzoin, and also a standard film, without pro-oxidant. After undergoing 96 and 144 h of UV light exposure, the blown films were evaluated by dilute solution viscometry, FTIR and SEM analysis. The results showed that the pro-oxidants lead to the formation of more macromolecular fragments containing carbonyl groups than in the standard PE film. The film extruded with benzoin showed greater fragmentation, which may be associated with a greater reduction in the average viscosimetric molar mass, therefore, this additive being a promising organic substance in the induction of photooxidation, as demonstrated by the other results obtained by FTIR and SEM.
为了减少环境中聚合物废料(如塑料袋)的积累,在聚烯烃(包括聚乙烯(PE),它是薄膜生产中使用最广泛的聚合物之一)中采用了促氧化剂。将这种添加剂加入PE薄膜的目的是在非生物降解过程中加速其氧化,生成含氧基团,从而促进生物降解。商业促氧化剂通常是过渡金属的有机盐。然而,它们的使用可能会导致一个次要问题,即过渡金属在聚合物废料堆放场地不当积累,因此,一直在寻找无金属且可生物降解的促氧化剂。在此背景下,本工作旨在评估通过挤出法制备的PE吹塑薄膜的光降解性能,所用材料包括一种商业促氧化剂d2w™、一种替代有机促氧化剂安息香以及一种不含促氧化剂的标准薄膜。在经过96小时和144小时的紫外线照射后,通过稀溶液粘度测定法、傅里叶变换红外光谱(FTIR)和扫描电子显微镜(SEM)分析对吹塑薄膜进行评估。结果表明,与标准PE薄膜相比,促氧化剂导致形成更多含羰基的大分子碎片。用安息香挤出的薄膜显示出更大程度的碎片化,这可能与粘均摩尔质量的更大降低有关,因此,正如FTIR和SEM获得的其他结果所示,这种添加剂是诱导光氧化的一种有前景的有机物质。