Catalyst for producing acrylonitrile

Details Catalyst for producing acrylonitrile Catalyst for producing acrylonitrile

2000-06-30

2003-07-22

Silverman, Stanley S. (Department: 1754)

Organic compounds -- part of the class 532-570 series

Organic compounds

Nitriles

C558S324000, C558S325000, C558S326000, C502S212000, C502S248000, C502S254000, C502S255000, C502S311000, C502S312000, C502S313000, C502S314000, C502S315000, C502S316000, C502S321000

Reexamination Certificate

active

06596897

ABSTRACT:

The present invention relates to a fluidized-bed catalyst for producing acrylonitrile by the ammoxidation of propylene.
The production of acrylonitrile by the ammoxidation has been developed for more than 30 years and a balance has been approached between the capacity of the acrylonitrile plants and the demand for acrylonitrile. Now the major development tendency of the production of acrylonitrile has been transformed from the construction of new devices to the reformation of existing plants in order to reduce the consumption of the feed stock and raise the capacity. By reformation of existing plants, change to effective catalysts and elimination of the bottleneck in the production process, it is possible to raise the capacity of acrylonitrile by 50-80%, while the investment required is only 20-30% of that of a newly constructed device. The economic benefit is enormous.
Two problems will arise in the reformation of the plant: (1) the reaction pressure in the fluidized reactor will rise; (2) the catalyst loading can not be too heavy. Therefore, the substitution catalyst should have a higher duty for propylene and the capability to endure higher reaction pressures.
The reaction pressure of the fluidized-bed reactor is determined by a resistance of a serious of heat exchangers, towers and piping between the outlet of the reactor and the top of the absorption tower. An increase in the capacity results in an appreciable increase in the amount of the effluent at the outlet of the reactor so that the aforesaid pressure drop is increased. Further, expanding of the heat conduction area in the heat exchangers contributes to additional pressure drop. To meet the requirement of the environmental protection, the waste gas from the top of the absorption tower is not allowed to purge into the atmosphere, and should be passed to a furnace to burn off. Thus, if a suction pump is not used, the pressure at the top of the absorption tower must be raised. Because of the various reasons mentioned above, the operation pressure of the prior reactor will be 0.5-1.0 times higher than the designed value, i.e., reach above 0.08 MPa.
The aforesaid second problem is the duty of the catalyst, i.e. WWH. The definition of WWH is the tons of propylene treated per ton of catalyst per hour. If the duty of the catalyst does not change, the catalyst loading should increase accordingly when the feed to the reactor increases. But the pipe of the cooling water is not high enough in the original design, and therefore the fluidized height in the reactor may exceed the height of the pipe of the cooling water. Moreover, the linear velocity in operation also appreciably increases because the feed to the reactor increases. The combined effect of the two changes may cause the rise of the temperature of the dilute phase in the reactor, the increase in the yield of carbon dioxide and the decrease in the selectivity to acrylonitrile. Therefore, higher WWH of the catalyst can prevent the aforesaid problems from accruing.
Theoretically, the ability of the catalyst to adsorb propylene should be enhanced by raising the WWH of the catalyst, but the theory that a certain element in a catalyst may enhance the ability to absorb propylene is not available. A catalyst with the following composition has been disclosed in the literature CN 1021638C:
A
a
B
b
C
c
Ni
d
Co
e
Na
f
Fe
g
Bi
h
M
i
Mo
j
O
x
where A represents potassium, rubidium, cesium, samarium or thallium, B represents manganese, magnesium, strontium, calcium, barium, lanthanum or rare earth; C represents phosphorus, arsenic, boron, antimony or chromium; M represents tungsten or vanadium.
A higher single-pass yield of acrylonitrile can be obtained on the above catalyst, but the duty for propylene is lower and the single-pass yield of acrylonitrile is greatly lowered under higher reaction pressures. Further research shows that components B and M in the above catalyst correlate to the duty and the high-pressure performance of the catalyst. Although some elements of component B act for raising the single-pass yield of acrylonitrile, they have negative effects on the duty and the high-pressure performance of the catalyst and unfavorable to the suitability to operations at higher pressures and higher duties. Moreover, It has been defined in CN 1021638C that the sum of i and j in the above catalyst composite is 12, i.e., a constant. This limitation is canceled in the present invention because according to this limitation, an increase in component M will result in a decrease in component Mo, and this will affect the single-pass yield of acrylonitrile. Moreover, the literature does not report data on the ammonium conversion. Experiments have approved that the ammonia conversion is about 92-93%, which is relatively low.
The objects of the present invention are to provide a novel catalyst for producing acrylonitrile, which is suitable for operations at higher reaction pressures and higher duties, maintains a high single-pass yield of acrylonitrile and has a high ammonia conversion, to overcome the problems of the catalyst of not being able to suit operations at higher reaction pressures and higher duties present in the above literature.
One object of the present invention is to provide a fluidized-bed catalyst for producing acrylonitrile by the ammoxidation of propylene, which comprises a silica carrier and a composite having the following formula:
A
a
C
c
D
d
Na
f
Fe
g
Bi
h
M
i
Mo
12
O
x
wherein A is at least one selected from the group consisting of potassium, rubidium, cesium, samarium, thallium and a mixture thereof; C is at least one selected from the group consisting of phosphorus, arsenic, boron, antimony, chromium and a mixture thereof; D is selected from nickel and cobalt or a mixture thereof; M is selected from tungsten, vanadium or a mixture thereof;
a is 0.01-1.0, c is 0.01-2.0, d is 0.01-12, f is 0.2-0.7, g is 0.01-8, h is 0.01-6, i is 0.01-9, x is the total number of the oxygen atom for meeting the requirement of the valence of the elements.
The carrier of the catalyst is silica, the content of which is 30-70% by weight.
Another object of the present invention is to provide a process for producing acrylonitrile by the ammoxidation of propylene at higher reaction pressure and higher duties, wherein the catalysts as above-said are used in a fluidized bed fulfilling the ammoxidation of propylene.
In the above technical solution, the preferred range of a is 0.03-0.4, the preferred range of c is 0.1-1.5, the preferred range of d is 0-8, the preferred range of f is 0.3-0.5, the preferred range of g is 0.1-4, the preferred range of h is 0.1-4, the preferred range of i is 0.1-6; the preferred range of the content of the silica carrier is 40-60% by weight.
There is no special requirement for the preparation procedure of the catalyst of the present invention and the catalyst can be prepared by the conventional procedure. First, various components are made into a solution, which is then made into a slurry by mixing with the carrier. The slurry is shaped into fine spheres via spray drying. Lastly, the fine spheres are calcined to obtain the catalyst. The preparation of the slurry is preferably made according to the procedure in CN 1005248C.
The chemicals for preparing the catalyst of the present invention are:
Component A is preferably the nitrate, hydroxide or salts that can decompose to oxides.
Phosphorus, arsenic, and boron of component C are preferably used in the form of their corresponding acids or ammonium salts. Chromium is preferably used in the form of chromium (III) oxide, chromium nitrate, or a mixture thereof. Antimony may be used in the form of antimony (III) oxide, antimony (V) oxide; antimony halides or antimony sol that are able to hydrolyze to antimony oxides.
Components nickel, cobalt, iron, bismuth can be used in the form of nitrates, oxides, or the salts that are able to decompose to oxides, but water-soluble nitrates are preferable.
Tungsten in component M can be used in the form of ammonium tungstate or tungsten oxide, and vanadium in the form of ammonium metava

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