对苯二甲酸
聚对苯二甲酸乙二醇酯
磺酸
材料科学
催化作用
水解
傅里叶变换红外光谱
解聚
对氨基苯甲酸
乙二醇
高分子化学
乙烯
核化学
化学
有机化学
化学工程
聚酯纤维
复合材料
工程类
作者
Iuliana M. Chirică,Anca G. Mirea,Tudor Şuteu,Andrei Kuncser,Ștefan Neațu,Mihaela Florea,Michel W. Barsoum,Florentina Neațu
标识
DOI:10.1021/acssuschemeng.4c01920
摘要
Plastics are indispensable materials for packaging and many products from our daily life, and their recycling is essential to ensure a circular economy. In this study, –SO3H-modified, Ti3C2-MXene was used as a recoverable solid acid catalyst for upcycling of polyethylene terephthalate (PET) to terephthalic acid (TPA) and ethylene glycol by hydrolysis. For the grafting of –SO3H groups to the Ti3C2Tx surface (where Tx represents the surface moieties, such as –OH or –O), sulfonation with an aryl diazonium salt obtained from sulfanilic acid was employed. X-ray photoelectron and Fourier transform infrared spectroscopy analyses provided a direct indication that sulfonation of the Ti3C2Tx was successfully performed, while X-ray diffraction and transmission electron microscopy analyses evidence the presence of –SO3H groups between the Ti3C2Tx layers due to the increases of the interlayer spacing through the intercalation of functional groups. The higher the concentration of acid groups, the higher the interlayer spacing. The depolymerization of PET in water occurred with a very good isolated yield in TPA (99%) for the MXene with the highest amount of sulfonic acid groups. We conclude that the acidity is mandatory to perform the hydrolysis reaction, in agreement with the acidity measurements, which show that the MXenes modified with the highest amount of derived sulfonic acids are the most active. Nevertheless, the accessibility to the acidic sites is a key factor that promotes the 2D acid-modified MXene materials as important catalysts for PET upcycling to TPA.
科研通智能强力驱动
Strongly Powered by AbleSci AI