TY - JOUR
T1 - Effective transesterification of triglyceride with sulphonated modified SBA-15 (SBA-15-SO3H)
T2 - Screening, process and mechanism
AU - Hu, Ningmeng
AU - Kong, Zhaoni
AU - He, Liang
AU - Ning, Ping
AU - Gu, Junjie
AU - Miao, Rongrong
AU - Sun, Xiangqian
AU - Guan, Qingqing
AU - Duan, Peigao
N1 - Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/10/1
Y1 - 2018/10/1
N2 - Different morphologies of ZrO2 were produced by different templates: ZrO2(CaCO3), ZrO2(C12H25SO3Na), ZrO2(C12H25SO4Na), ZrO2(CTAB), and solid superacids, such as ZrO2/SBA-15, SO42-/ZrO2, SO42-/ZrO2/SBA-15, and SBA-15-SO3H. The catalytic transesterification activities of these catalysts were tested. The more highly acidic catalysts and higher surface areas led to higher catalytic activity. In particular, the conversion yield of triglyceride reached 90.1% and was maintained for 90 min at 200 °C with 5.0 wt% SBA-15-SO3H, indicating this material to be one of most effective acid catalysts for the transesterification process. The mechanism indicated that the most important process was the abstraction of hydrogen from alcohols and α-substituted carboxylic glycerides. In the initial transesterification, the alcohol hydrogen atoms could be attracted onto the surface. Then, the nucleophilic attack of the alcohol led to the α-substituted carboxylic glyceride. Finally, monoglycerides, diglycerides or glycerine were released from the surface by proton (H+) replacement.
AB - Different morphologies of ZrO2 were produced by different templates: ZrO2(CaCO3), ZrO2(C12H25SO3Na), ZrO2(C12H25SO4Na), ZrO2(CTAB), and solid superacids, such as ZrO2/SBA-15, SO42-/ZrO2, SO42-/ZrO2/SBA-15, and SBA-15-SO3H. The catalytic transesterification activities of these catalysts were tested. The more highly acidic catalysts and higher surface areas led to higher catalytic activity. In particular, the conversion yield of triglyceride reached 90.1% and was maintained for 90 min at 200 °C with 5.0 wt% SBA-15-SO3H, indicating this material to be one of most effective acid catalysts for the transesterification process. The mechanism indicated that the most important process was the abstraction of hydrogen from alcohols and α-substituted carboxylic glycerides. In the initial transesterification, the alcohol hydrogen atoms could be attracted onto the surface. Then, the nucleophilic attack of the alcohol led to the α-substituted carboxylic glyceride. Finally, monoglycerides, diglycerides or glycerine were released from the surface by proton (H+) replacement.
KW - Biodiesel
KW - SBA-15-SOH
KW - Transesterification
KW - Triglyceride
UR - https://www.scopus.com/pages/publications/85050754661
U2 - 10.1016/j.ica.2018.07.032
DO - 10.1016/j.ica.2018.07.032
M3 - 文章
AN - SCOPUS:85050754661
SN - 0020-1693
VL - 482
SP - 846
EP - 853
JO - Inorganica Chimica Acta
JF - Inorganica Chimica Acta
ER -