LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

γ-Valerolactone converting to butene via ring-opening and decarboxylation steps over amorphous SiO2-Al2O3 catalyst

Photo from wikipedia

Abstract 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,… Click to show full abstract

Abstract 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.

Keywords: sio2 al2o3; butene; amorphous sio2; ring opening; al2o3 catalyst

Journal Title: Molecular Catalysis
Year Published: 2020

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.