Gas and liquid phase catalytic Beckmann rearrangement of oximes to produce lactams
View Patent ↗Methods for producing lactams from oximes by performing a Beckmann rearrangement using a silicoaluminophosphate catalyst are provided. These catalysts may be used in gas phase or liquid phase reactions to convert oximes into lactams. High conversion of oxime and high selectivity for the desired lactams are produced using the disclosed methods, including high conversion and selectivity for ε-caprolactam produced from cyclohexanone oxime and high conversion and selectivity for ω-laurolactam produced from cyclododecanone oxime.
1. A catalyst comprising:
a silicon-containing aluminophosphate framework with the IZA framework code FAU; and
a plurality of discrete Brønsted acid sites positioned in an interior of the framework, the acid sites comprising silicon isomorphously substituted for phosphorous in the framework;
wherein the catalyst is a SAPO-37 type catalyst, and the catalyst is formed from a gel having a molar ratio of silicon to phosphorous from 0.21:1 to 0.42:1.
2. The catalyst of claim 1 , wherein the silicon comprises about 1 wt. % to about 10 wt. % of the total weight of the catalyst.
3. The catalyst of claim 2 , wherein the silicon comprises about 2 wt. % to about 9.1 wt. % of the total weight of the catalyst.
4. A silicoaluminophosphate catalyst having a microporous crystalline framework structure having a composition on an anhydrous basis of:
mR:(Si x Al y P z )O 2
wherein:
R is at least one organic templating agent;
m is from 0.02 to 0.3; and
x, y, and z, are selected within the values bounded by the points A, B, C, D, and E on a ternary diagram, where:
x
y
z
A
0.01
0.47
0.52
B
0.94
0.01
0.05
C
0.98
0.01
0.01
C
0.39
0.60
0.01
E
0.01
0.60
0.39
the catalyst comprising a plurality of discrete Brønsted acid sites positioned in an interior of the framework, the acid sites comprising silicon isomorphously substituted for phosphorous in the framework; wherein the ratio of silicon to phosphorous is from 0.21:1 to 0.42:1.
5. The catalyst of claim 4 , wherein x, y, and z, are selected within the values bounded by the points a, b, c, d, and e on a ternary diagram, where:
x
y
z
a
0.02
0.49
0.49
b
0.25
0.37
0.38
c
0.25
0.48
0.27
d
0.13
0.60
0.27
e
0.02
0.60
0.38.
6. The catalyst of claim 5 , wherein the catalyst is a SAPO-37 catalyst.
7. The catalyst of claim 4 , wherein the catalyst is a silicon-containing aluminophosphate framework with the IZA framework code FAU.
8. The catalyst of claim 4 , wherein the at least one organic templating agent is at least one of tetrmethylammonium hydroxide pentahydrate and tetrapropylammonium hydroxide.
9. The catalyst of claim 4 , wherein the silicon comprises about 1 wt. % to about 10 wt. % of the total weight of the catalyst.
10. A method of forming a SAPO-37 catalyst, comprising:
adding an aluminum source to a phosphorous source to form an aluminum/phosphorous mixture;
dissolving tetrmethylammonium hydroxide pentahydrate in tetrapropylammonium hydroxide to form a TMAOH/TPAOH solution;
adding fumed silica to the TMAOH/TPAOH solution to form a structural template solution;
adding the structural template solution to the aluminum/phosphorous mixture to form a gel having a ratio of silicon to phosphorous from 0.21:1 to about 0.42:1; and
heating the gel to form the catalyst, the catalyst having a silicon-containing aluminophosphate framework with the IZA framework code FAU and a plurality of discrete Brønsted acid sites positioned in an interior of the framework, the acid sites comprising silicon isomorphously substituted for phosphorous in the framework.
11. The method of claim 5 , wherein the aluminum source is aluminum oxide and the phosphorous source is phosphoric acid.
12. The method of claim 5 , further comprising:
isolating a product by at least one of centrifuging, filtering, or washing the catalyst; and
drying the isolated catalyst.