Na Sun, Minhua Zhang, Xiuqin Dong, Lingtao Wang
Key Laboratory for Green Chemical Technology of Ministry of Education, R&D Center for Petrochemical Technology, Tianjin University Tianjin 300072 China
Collaborative Innovation Center of Chemical Science and Engineering Tianjin 300072 China.
RSC Adv. 2019 May 21;9(28):15941-15948. doi: 10.1039/c9ra02546d. eCollection 2019 May 20.
Sulfonated ordered mesoporous carbon (SOH-OMC) solid acid catalysts from sucrose were prepared using hard-template method, and their catalytic performance as well as the deactivation mechanism for esterification of free fatty acids (FFAs) in waste cooking oils (WCOs) were evaluated. Effects of sulfonation time, sulfonation temperature and hard template structure type for the textural properties and acid properties of SOH-OMC were systematically investigated by N adsorption-desorption, FT-IR, NH-TPD, TEM and strong acid density analysis. The results indicated that, SOH-OMC(s)-6-160 catalyst, which was prepared by using SBA-15 as hard template at sulfonation time of 6 h and sulfonation temperature of 160 °C, had well-ordered mesoporous structure and high -SOH groups density (2.32 mmol g). Compared with SOH-APC-6-160 catalyst, cation-exchange resin D072 and SOH-OMC(k)-6-160 catalyst, it was found that the SOH-OMC(s)-6-160 catalyst exhibited highest activity (FFAs conversion was 93.8%) and good stability for the FFAs esterification, attributed to its 2D-hexagonal channels and hydrophobic surface. The -SOH groups being leached out of SOH-OMC catalysts into the liquid phase (especially methanol) would be the main reason causing catalyst deactivation.
采用硬模板法制备了以蔗糖为原料的磺化有序介孔碳(SOH-OMC)固体酸催化剂,并对其在废食用油(WCO)中游离脂肪酸(FFA)酯化反应中的催化性能及失活机理进行了评价。通过N吸附-脱附、傅里叶变换红外光谱(FT-IR)、氨程序升温脱附(NH-TPD)、透射电子显微镜(TEM)和强酸密度分析,系统研究了磺化时间、磺化温度和硬模板结构类型对SOH-OMC织构性质和酸性的影响。结果表明,以SBA-15为硬模板,在磺化时间为6 h、磺化温度为160℃条件下制备的SOH-OMC(s)-6-160催化剂具有规整的介孔结构和较高的-SOH基团密度(2.32 mmol g)。与SOH-APC-6-160催化剂、阳离子交换树脂D072和SOH-OMC(k)-6-160催化剂相比,发现SOH-OMC(s)-6-160催化剂在FFA酯化反应中表现出最高的活性(FFA转化率为93.8%)和良好的稳定性,这归因于其二维六方孔道和疏水表面。SOH-OMC催化剂中的-SOH基团被浸出到液相(尤其是甲醇)中是导致催化剂失活的主要原因。