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γ-Valerolactone converting to butene via ring-opening and decarboxylation steps over amorphous SiO2-Al2O3 catalyst
Molecular Catalysis ( IF 4.6 ) Pub Date : 2020-10-03 , DOI: 10.1016/j.mcat.2020.111218
Hongtao Wang , Yushan Wu , Shuai Guo , Chenglong Dong , Mingyue Ding

γ-Valerolactone (GVL) as a sustainable platform compound could be converted to renewable fuels and chemicals, whereas directly converting GVL to target products remains still the challenge. In this work, we report an amorphous SiO2-Al2O3 catalyst with adjustable acidity, which presented an excellent selectivity of 97.5 % butene at GVL conversion of 99.5 %, and remained an outstanding stability for 50 h. Appropriate weak and strong acid sites were the key for the ring-opening of GVL. Lower acid sites facilitated the decarboxylation of pentenoic acid (PEA), while higher acid sites promoted the cracking of PEA. Besides, a two-stage integration system was developed for converting GVL to C5+ hydrocarbons via butene intermediate, giving a good yield of 57.6 % C5+ hydrocarbons via combining the SiO2-Al2O3 catalyst with nano-HZSM-5 together.



中文翻译:

在非晶态SiO 2 -Al 2 O 3催化剂上通过开环和脱羧步骤将γ-戊内酯转化为丁烯

γ-戊内酯(GVL)作为可持续的平台化合物可以转化为可再生燃料和化学品,而直接将GVL转化为目标产品仍然是挑战。在这项工作中,我们报告了一种具有可调酸度的无定形SiO 2 -Al 2 O 3催化剂,该催化剂在99.5%的GVL转化率下具有97.5%的优良丁烯选择性,并在50小时内保持了出色的稳定性。适当的弱酸和强酸位点是GVL开环的关键。较低的酸位促进戊烯酸(PEA)的脱羧,而较高的酸位促进PEA的裂解。此外,还开发了用于将GVL转换为C 5 +的两级集成系统通过将SiO 2 -Al 2 O 3催化剂与纳米HZSM-5结合在一起,可通过丁烯中间体形成烃,得到57.6%C 5 +烃的良好收率。

更新日期:2020-10-04
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