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Synthesis TS-1 nanozelites via L-lysine assisted route for hydroxylation of Benzene.
- Source :
-
Molecular Catalysis . Aug2021, Vol. 512, pN.PAG-N.PAG. 1p. - Publication Year :
- 2021
-
Abstract
- • TS-1 nanozeolite was achieved in a concentrated gel system through a two-step synthesis method. • The effect of the addition of L-lysine on the structure of zeolite was proposed. • The formation mechanism of nanozeolite was speculated. • TS-1 nanozeolite showed the excellent catalytic performance in hydroxylation of benzene. L-lysine is used as a crystallization regulator, and a two-step synthesis method is adopted in a concentrated gel system, which provides a new route to synthesize of nano-sized TS-1 zeolite. The new synthesis strategy was used to successfully synthesize TS-1 zeolite with a particle size less than 100 nm. The rate of crystal nucleation is faster than the crystal growth at the low temperature in the first step. Introduction of L-lysine can prevent crystal growth to form nano-sized TS-1 zeolite at the high temperature in the second step. Meanwhile, L-lysine decrease the pH value of the gel system, which is favorable for Ti atoms to incorporate the TS-1 framework. TS-1 nanozeolite can effectively reduce the diffusion resistance, and nanozeolite has a large specific surface area and high stability. Therefore, TS-1 nanozeolite exhibits the excellent catalytic performance during the hydroxylation of benzene. The conversion of benzene has been greatly improved and the types of by-products are effectively reduced. The conversion of benzene reached 50.2%, and the yield of phenol was 30.8% without by-product benzoquinone. TS-1 nano-zeolite as a catalyst for benzene hydroxylation shows great potential in industrial application. [Display omitted] [ABSTRACT FROM AUTHOR]
- Subjects :
- *BENZENE
*LYSINE
*HYDROXYLATION
*NUCLEATION
*PARTICLE size determination
Subjects
Details
- Language :
- English
- ISSN :
- 24688231
- Volume :
- 512
- Database :
- Academic Search Index
- Journal :
- Molecular Catalysis
- Publication Type :
- Academic Journal
- Accession number :
- 162177982
- Full Text :
- https://doi.org/10.1016/j.mcat.2021.111779