Single reactor process for preparing acrylic acid from...

Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acids and salts thereof

Reexamination Certificate

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C562S542000, C562S545000

Reexamination Certificate

active

06384274

ABSTRACT:

This invention relates to an improved process for preparing acrylic acid from propylene using a single reactor. In particular, the invention relates to a single reactor process for preparing acrylic acid from propylene utilizing an increased concentration of propylene reactant thereby providing increased capacity and throughput.
The preparation of acrylic acid from propylene generally proceeds in a vapor phase two step catalytic oxidation reaction. In the first step propylene is oxidized in the presence of oxygen, diluent inert gasses, water vapor, and appropriate catalysts to produce acrolein according to equation (I):
C
3
H
6
+O
2
C
2
H
3
CHO+H
2
O+heat  (I).
The acrolein is then oxidized, in a second step, in the presence of oxygen, diluent inert gasses, water vapor, and appropriate catalysts to form acrylic acid according to equation (II):
C
2
H
3
CHO+½ O
2
C
2
H
3
COOH+heat  (II).
The two stage vapor phase catalytic oxidation of propylene to acrylic acid is generally performed using either tandem reactors wherein a separate reactor is utilized for each step (e.g., see the description in U.S. Pat. No. 4,873,368) or by utilizing one reactor to perform both steps (e.g., see the description in U.S. Pat. No. 4,526,783).
The acrylic acid prepared using such a vapor phase catalytic oxidation reaction is present in a mixed product gas exiting the reactor. Generally, the mixed product gas is cooled and is contacted with an aqueous stream in an absorption tower, thereby providing an aqueous acrylic acid solution from which acrylic acid can be isolated and purified. The remainder of the product gasses, known as the absorber waste gas or absorber off-gas, is incinerated or undergoes waste treatment. Depending on the reactants feed gas composition, the absorber off-gas may contain inert gasses, O
2
, water vapor, CO, CO
2
, unreacted propylene, unreacted acrolein and/or acrylic acid.
It is known in the art to recycle at least a portion of the absorber off-gas back to the reactor(s) to provide inert diluent gas and steam to the reactant composition. The propylene in the reactant composition must be diluted because at high propylene concentrations the reaction may proceed too quickly and become difficult to control. Recycle of the absorber off-gas provides the necessary diluent gasses and steam to the reactor feed to assure a suitable propylene concentration. In addition, recycling the absorber off-gas serves to reduce waste water generated by the process by reducing the amount of steam that is fed to the process. Furthermore, small amounts of unreacted propylene and acrolein contained in the off-gas are given another chance to react and thereby improve the overall acrylic acid yield by optimizing conversions of propylene and acrolein.
When absorber off-gas recycle is not used, steam and nitrogen are used as the primary diluents. Steam is not consumed, but may alter the selectivity, conversion and/or catalytic activity in the oxidation reactions and is part of the mixed product gasses emerging from the reactor. When the mixed product gasses are introduced into the absorption column, the steam substantially condenses tat the bottom of the absorption column and is a small part of the gasses flowing through the absorber.
However, a problem arises with absorber off-gas recycle. In contrast to the situation wherein absorber off-gas recycle is not used, a load develops at the top of the absorber because of the increased volume of inert gas flowing through the absorber. When absorber off-gas recycle is utilized, the off-gas is predominantly an inert gas such as nitrogen. When mixed product gasses containing such inert gasses are introduced into the absorber they do not generally condense at the absorber bottom, but rather remain part of the product gasses flowing through the absorber. Consequently, the increased inert gas content in the mixed product gasses introduced into the absorber causes an increase in the velocity of the gas flowing through the absorber. This results in a load at the top of the absorber. As the gas velocity gets higher, an increasing amount of product acrylic acid will remain with the absorber off-gas and be either lost to waste or be recycled back to the reactor. When it is recycled back to the reactor it can cause a decrease in catalyst activity. Consequently, regardless of whether it is lost to waste or recycles back to the reactor, the net result is a drop in acrylic acid yield.
A further problem results from the need to dilute the propylene in the gas feed to a manageable concentration. The dilution may be effected by absorber off-gas recycle or by adding steam and other inert materials or both. Because the two step oxidation of propylene to acrylic acid is highly exothermic, as the propylene concentration gets higher the danger of a runaway combustion increases. Also, the reaction mixture could become flammable and explode if ignited. Consequently, the oxidation of propylene to acrylic acid is generally practiced in the art utilizing a propylene concentration in the reactant gas feed composition of between 4 and 7 volume percent of the total reactant feed composition (see for example col. 2, lines 42-46 of U.S. Pat. No. 4,873,368). Accordingly, to assure control of the oxidation, propylene is diluted with steam and/or inert gasses such as nitrogen and combined with oxygen to form the feed composition. As a result, there is an additional load on the compressor which limits the capacity of the system. Consequently, any increase in capacity would require a larger compressor to handle the larger load.
As a result of the extra load on the absorber and on the compressor there is a limit on the capacity of the system which heretofore could not be remedied except by installation of larger equipment.
A further problem exists when tandem reactors are utilized. In tandem reactors there exists a high volume interstage between the two reactors through which the acrolein produced in the first reactor passes to the second reactor. This results in a longer residence time, compared to a single reactor, of the acrolein product in the interstage which may lead to homogenous reactions of acrolein and/or formation of foulants. Foulants may be formed by, for example, corrosion and deposition processes. Such homogeneous reactions are generally not catalytic, but rather are free radical reactions of acrolein which produce carbon oxides such as carbon dioxide and carbon monoxide, as well as other products such as acetaldehyde. Consequently, because of the longer interstage residence time in a tandem reactor process, steps such as cooling, reaction quenching, and acrolein dilution must be taken to reduce such homogeneous reactions of acrolein. In addition, the equipment and piping of the interstage is susceptible to gas leaks.
U.S. Pat. Nos. 4,365,087 and 4,873,368 have dealt with the problem of increasing process productivity/capacity by raising the propylene concentration level. However, the processes in these references used a tandem reactor process whereby either the temperature of the feed was limited (<260° C.), the oxygen to propylene ratio (1.1-2.0:1, preferably lower than 1.8) was kept low, additional oxygen and inert gas was fed to the second stage reactor, and the reaction was quenched somewhat before introduction to the second stage ('087) or the oxygen to propylene ratio (1.17-1.66:1) was even lower, additional oxygen and inert gas was fed to the second stage reactor, and the reaction was quenched somewhat before introduction to the second stage. Accordingly, the basis of the technique relied on two mechanisms for controlling the reaction at higher propylene concentrations:
(1) tightly controlling the temperature before entry into the first stage reactor and/or the second stage reactor; and
(2) limiting the amount of oxygen initially available to the first reactor for oxidation of propylene to acrolein and then adding more oxygen and diluent at the interstage before the second stage reactor so that the second reacto

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