Agarwal Ashutosh, Li Xue
Department of Environment and Energy Engineering, Chonnam National University, Gwangju 61186, Republic of Korea.
Engineering Product Development, Singapore University of Technology and Design, 8 Somapah Road, 487372, Singapore.
Nanoscale. 2024 Apr 4;16(14):7019-7030. doi: 10.1039/d4nr00358f.
In this study, Kraft lignin-derived bio-oil was upgraded with LiCoO or CoO-impregnated hierarchical nano-ZSM-5 catalysts. The synthesized catalysts were characterized by N-Ads-Des, XRD, XPS, NH-TPD, FTIR, FESEM and ICP-OES analyses. Upon incorporation of LiCoO and CoO onto the HZSM-5 support, the MFI structure of HZSM-5 remained intact. All the catalysts displayed a combination of Type-I and -IV isotherms. The upgraded bio-oil showed a significant increase in the amounts of alkylated guaiacols owing to the reduction in unsubstituted guaiacols, alkenyl guaiacols, and homovanillic acid. Hydrogenation, alkylation, and deoxygenation were the plausible bio-oil upgrading pathways. With the increase in cobalt content, weak acidity decreased through all the catalysts, while LiCoO provided supplementary acid sites that increased the total acidity of LiCoO/HZSM-5 compared to the CoO/HZSM-5 catalyst. LiCoO/HZSM-5 with a low cobalt content (5% and 10% Co) displayed high selectivity for the production of alkylated guaiacols owing to their strong acidity. The upgraded bio-oils showed an increase in carbon and hydrogen followed by a decrease in oxygen content. The maximum higher heating value (∼29.83 MJ kg) was obtained for the 10% Co (LiCoO)/HZSM-5 catalyst. In general, LiCoO/HZSM-5 outperformed the CoO/HZSM-5 catalyst. XRD of the spent 10% Co (LiCoO)/HZSM-5 suggested the complete loss of lithium from the catalyst with the retention of the MFI structure of the HZSM-5 support. In this study, it was successfully demonstrated that the main constituent of the cathode material of spent lithium-ion batteries LiCoO could be employed to synthesize a novel and cheap catalyst for bio-oil upgrading while addressing the e-waste management issue in a sustainable manner.
在本研究中,采用浸渍有LiCoO或CoO的分级纳米ZSM-5催化剂对硫酸盐木质素衍生生物油进行提质。通过N2吸附-脱附、XRD、XPS、NH3-TPD、FTIR、FESEM和ICP-OES分析对合成的催化剂进行了表征。将LiCoO和CoO负载到HZSM-5载体上后,HZSM-5的MFI结构保持完整。所有催化剂均呈现I型和IV型等温线的组合。提质后的生物油中,由于未取代的愈创木酚、烯基愈创木酚和高香草酸的减少,烷基化愈创木酚的含量显著增加。氢化、烷基化和脱氧是可能的生物油提质途径。随着钴含量的增加,所有催化剂的弱酸位减少,而LiCoO提供了补充酸位,与CoO/HZSM-5催化剂相比,增加了LiCoO/HZSM-5的总酸度。低钴含量(5%和10% Co)的LiCoO/HZSM-5由于其强酸性,对烷基化愈创木酚的生产表现出高选择性。提质后的生物油碳和氢含量增加,氧含量降低。10% Co (LiCoO)/HZSM-5催化剂的最高高热值(约29.83 MJ kg)。总体而言,LiCoO/HZSM-5的性能优于CoO/HZSM-5催化剂。使用过的10% Co (LiCoO)/HZSM-5的XRD表明,催化剂中的锂完全流失,而HZSM-5载体的MFI结构得以保留。在本研究中,成功证明了废旧锂离子电池正极材料的主要成分LiCoO可用于合成新型廉价的生物油提质催化剂,同时以可持续的方式解决电子垃圾管理问题。