Polidoro Daniele, Perosa Alvise, Rodríguez-Castellón Enrique, Canton Patrizia, Castoldi Lidia, Rodríguez-Padrón Daily, Selva Maurizio
Dipartimento di Scienze Molecolari e Nanosistemi, Università Ca' Foscari di Venezia, 30123 Venezia, Italy.
Department of Inorganic Chemistry, Facultad de Ciencias, Universidad de Málaga, Campus de Teatinos s/n, 29071 Málaga, Spain.
ACS Sustain Chem Eng. 2022 Sep 29;10(41):13835-13848. doi: 10.1021/acssuschemeng.2c04443. eCollection 2022 Oct 17.
High anthropogenic CO emissions are among the main causes of climate change. Herein, we investigate the use of CO for the synthesis of organic cyclic carbonates on metal-free nitrogen-doped carbon catalysts obtained from chitosan, chitin, and shrimp shell wastes, both in batch and in continuous flow (CF). The catalysts were characterized by N physisorption, CO-temperature-programmed desorption, X-ray photoelectron spectroscopy, scanning electron microscopy, and CNHS elemental analysis, and all reactivity tests were run in the absence of solvents. Under batch conditions, the catalyst obtained by calcination of chitin exhibited excellent performance in the conversion of epichlorohydrin (selected as a model epoxide), resulting in the corresponding cyclic carbonate with 96% selectivity at complete conversion, at 150 °C and 30 bar CO, for 4 h. On the other hand, in a CF regime, a quantitative conversion and a carbonate selectivity >99% were achieved at 150 °C, by using the catalyst obtained from shrimp waste. Remarkably, the material displayed an outstanding stability over a reaction run time of 180 min. The robustness of the synthetized catalysts was confirmed by their good operational stability and reusability: ca. (75 ± 3)% of the initial conversion was achieved/retained by all systems, after six recycles. Also, additional batch experiments proved that the catalysts were successful on different terminal and internal epoxides.
高人为源一氧化碳排放是气候变化的主要原因之一。在此,我们研究了一氧化碳在以壳聚糖、几丁质和虾壳废料为原料制得的无金属氮掺杂碳催化剂上用于合成有机环状碳酸酯的情况,包括间歇式和连续流(CF)模式。通过氮物理吸附、一氧化碳程序升温脱附、X射线光电子能谱、扫描电子显微镜和CNHS元素分析对催化剂进行了表征,所有反应测试均在无溶剂条件下进行。在间歇条件下,通过煅烧几丁质得到的催化剂在环氧氯丙烷(选为模型环氧化物)的转化中表现出优异性能,在150℃、30巴一氧化碳压力下反应4小时,完全转化时相应环状碳酸酯的选择性为96%。另一方面,在连续流模式下,使用从虾废料制得的催化剂,在150℃时实现了定量转化且碳酸酯选择性>99%。值得注意的是,该材料在180分钟的反应运行时间内表现出出色的稳定性。合成催化剂的稳健性通过其良好的操作稳定性和可重复使用性得到证实:经过六次循环后,所有体系均实现/保留了约(75±3)%的初始转化率。此外,额外的间歇实验证明这些催化剂对不同的末端和内环氧化物均有效。