[0001] Recovery and purification systems for acrylonitrile and methacrylonitrile obtained
by the ammoxidation of propylene or isobutylene are well known. See for example U.S.
patent numbers 3,433,822; 3,399,120; 3,535,849; and 3,936,360. The gaseous reactor
effluent from an ammoxidation reactor is first directly contacted with a quenching
liquid to cool the effluent and remove a substantial amount of contaminates produced
during the reaction, such as polymers. The cooled gaseous quench effluent is typically
sent to a washing column or absorber wherein the gaseous effluent is contacted with
water. The liquid stream from the bottom or the absorber containing the various nitriles,
water and some impurities is then sent to a distillation column. Solvent water is
used to extractively distill this stream, producing an overhead vapor stream of acrylonitrile.
As described in U.S. 3,999,120, the bottoms of the extractive distillation column
may then be sent to a second stripping column. The overhead of this stripping.column
contains acetonitrile with a minor amount of water, and the liquid bottoms stream
contains water and impurities. An alternate method of recovery, also found in this
reference, is the removal of a sidestream from the extractive distillation column.
This stream containing mostly acetonitrile and water, is sent to a smaller stripping
column with acetonitrile being removed overhead and the liquid bottoms containing
mostly water being returned to the extractive distillation column. When this method
of recovery is used the liquid bottoms stream from the extractive distillation column
is mostly water and impurities with traces of acetonitrile.
[0002] Heat necessary to perform the recovery operations is applied to the bottem of both
the extractive distillation column and the stripping column. Unfortunately, this heat,
usually applied by using an indirect reboiler, brings about polymerization of the
impurities found in the associated columns.
[0003] Waste disposal of these bottoms streams is both difficulat and costly. The solids
content of the stream due to the polymerization is so high that it prevents normal
waste water treatment. Further, the size of these streams are very large, thus requiring
large specialized equipment. For example, German Patent No. 050,722 discloses a method
for purification of this waste water using a separate distillation column and large
amounts of steam to evaporate the water, thus reducing the size of the latter specialized
waste treatment facilities.
[0004] The present invention provides a unique method for reducing the size of these troublesome
streams with very little capital investment or operating costs.
[0005] It has now been discovered that in the process for the recovery and purification
of acrylonitrile or methacrylonitrile produced by the ammoxidation'reaction of propylene
or isobutylene, molecular oxygen and ammonia in the presence of ammoxidation catalysts,
comprising:
a) contacting the ammoxidation reactor effluent conatining acrylonitrile or methacrylonitrile,
acetonitrile, and impurities with an equeous quench liquid in a quench system to produce
a gaseous quench effluent from said quench system;
b) absorbing said gaseous quench effluent in water to form an aqueous solution;
c) feeding the aqueous solution to an intermediate tray of a first column having a
plurality of trays, using solvent water introduced in the top of said first co..umn
to perform a water extractive distillation, wherein a first overhead vapor stream
of aciylo- nitrile or methacrylonitrile with some water is removed from the top of
the first column, and a liquid stream containing acetonitrile. impurities and water
is removed from the bottom of the first column;
d) feeding at least a part of the liquid bottoms from said first column to a second
column wherein distillation is performed to remove a second overhead vapor stream
of acetonitrile and water from the top of the second column, and a second liquid stream
containing water and impurities from the bottom of the second column,
e) feeding at least part of the second liquid bottoms stream to the quench system
of (a) as the aqueous quench liquid, the improvement comprising: removing a vapor
stream from the lower fourth of said second column.
[0006] In another embodiment, the invention may be additionally stated as in the process
for the recovery and purification of acrylonitrile or methacrylonitrile produced by
the ammoxidation reaction of propylene or isobutylene, molecular oxygen and ammonia
in the presence of ammoxidation catalysts, comprising:
a) contacting the ammoxidation reactor effluent effluent containing acrylonitrile
or methacrylonitrile, acetonitrile, and impurities with an aqueous quench liquid in
a quench system to produce a gaseous quench effluent from said quench system:
b) absorbing said gaseous quench effluent in water to form an aqueous solution;
c) feeding the aqueous solution to an intermediate tray of a distillation column having
a plurality of trays, using solvent water introduced in the top of said column to
perform a water extractive distillation, wherein an overhead vapor stream of acrylonitrile
with some water is removed from the top of the column, and a liquid stream containing
water and impurities is removed from the bottom of the column.
d) removing a first side stream from the lower half of said column to recover acetonitrile;
e) feeding at least a part of the liquid bottoms from said column to the quench system
as quench liquid, the improvement -comprising: removing a vapor stream containing
water from the lower fourth of said column.
[0007] The reactor effluent gas, usually at a temperature between 700° and 900°F, is first
passed to a quench system. The purpose of the quench system is to remove excess ammonia,
polymers and heavier impurities produced by the reaction, and to cool the reactor
effluent gas. Typically water with some sulfuric acid is used as a quench liquid.
The reactor effluent gas leaves the quench system at a temperature of about 90° to
about 230°F. A bottom stream containing water; acid, polymers and other impurities
is removed from the quench system. This stream poses very difficult waste disposal
problems. Because of the large amount of solids and other impurities in this stream,
it cannot be sent to an activated sludge processor or biopond for treatment. Typical
methods of treatment in the past have been deep well injection or incineration. As
stated in the Background, other methods such as another distillation column have been
used in attempts to reduce the size of this stream. It is an object of the present
invention to reduce the size of the quench bottom stream and thus reduce the cost
of purification.
[0008] After being cooled in the quench system, the reactor effluent gases are then passed
to an absorber or wash column. Here the effluent gases are contacted with water. The
water absorbs acrylonitrile or methacrylonitrile, acetonitrile and some impurities.
This aqueous solution is removed from the bottom of the wash column. Non-absorbed
gases are removed as a vapor stream from the top of the wash column.
[0009] The aqueous solution from the bottom of the absorber is then sent to further processing
to recover acrylonitrile and acetonitrile. This processing is normally done in one
of two ways.
[0010] First, the aqueous solution is sent to an extractive distillation column. This column
typically contains 60-120 trays. Solvent water is added to the top of the column and
passes countercurrent to the feed. Heat is applied to the bottom of the column, usually
be an indirect heat exchanger. Acrylonitrile and HCN are removed as a vapor stream
from the top of the column. This stream then.goes to further processing to purify
the acrylonitrile. Acetonitrile, water and impurities are removed from the bottom
of the extractive distillation column and passed to a stripper. In the stripper, large
amounts of steam are used to separate the acetonitrile from the water. Acetonitrile
is removed as a vapor stream overhead. A bottom stream containing water and impurities
is then removed from the stripper and used as the quench liquid in the quench column.
[0011] The large amounts of heat necessary to strip the acetonitrile from the water solution
also has the undesirable result of polymerizing certain impurities. This polymerization
makes waste disposal of the bottom stream extremely difficult.
[0012] The present invention greatly reduces the size of the bottom stream by removing a
vapor stream from the lower fourth of the stripper. This vapor stream is mainly water
with very little if any acetonitrile or impurities. The vapor stream, when condensed,
is thus free of solids and hence can be fed to such waste disposal systems as an activated
sludge processor or biopond for further treatment. The much reduced bottom stream
from the stripper is then sent to the quench column as previously described.
[0013] It is preferred that the vapor stream be removed from bleow the first tray of the
column. However, the present invention's vapor stream may be taken from anywhere in
the lower fourth of said column.
[0014] Where a liquid return is removed from the column as recycle to the acrylonitrile
extractive distillation column, the vapor stream should be removed from below this
liquid stream.
[0015] A second method of purifying the aqueous solution from the absorber is to pass this
solution to a somewhat different extractive distillation column. This column, similar
to the one previously described, removes a sidestream containing acetonitrile from
the lower half of the column. This sidestream is sent to a much smaller stripping
column, usually consisting of 20-30 trays. Acetonitrile is removed as an overhead
vapor while the liquid bottoms is returned to the extractive distillation column.
The bottoms of this modified extractive distillation column is similar to the bottoms
stream issuing from the stripper as discussed above. The present invention is also
applicable to this method of recovery by removing a vapor stream from the lower fourth
of the extractive distillation column. This again has the advantage of greatly reducing
the bottoms stream.
[0016] Figures 1 and 2 are schematic representations of the present invention as applied
to acrylonitrile showing two methods of recovery.
[0017] Referring to Figure 1, the reactor effluent gas in conduit 100 containing acrylonitrile,
HCN, acetonitrile, water vapor and impurities is first passed to a quench column 102.
The gas is contacted with quench liquid 130 in the quench column. A bottoms stream
containing water and impurities is removed through conduit 106 and sent to waste treatment.
[0018] The cooled reactor effluent gases leave the quench system through line 108 and pass
as feed to the absorber 110. Wash water enters the absorber at the top through line
112. Non-condensible gases are removed from the absorber through line 114. An aqueous
solution containing water, acrylonitrile, acetonitrile and impurities are removed
as a bottoms stream through line 116 and passed to the extractive distillation column
118.
[0019] Solvent water is introduced to the top of column 118 through line 120 to perform
extractive distillation. Acrylonitrile and HCN is removed as an overhead vapor through
line 122 and sent to further purification (not shown). A bottoms stream containing
acetonitrile and water is removed through line 124 and passed to stripper 126. Heat
is added to the stripper to remove acetonitrile as an overhead vapor through line
128. The bottoms stream containing water, polymers and other impurities are removed
through line 130 and sent back to the quench system. A vapor stream is removed via
line 132 just below the first tray of this column. This vapor stream, containing mostly
water, can then be condensed and sent to typical waste treatment facilities such as
a sludge processor or biopond. The removal of this vapor stream greatly reduces the
amount of water issuing from the bottom of the stripper.
[0020] Additionally, a liquid stream may be removed from the lower half of the stripper
through line 120 and used as solvent water to the extractive distillation column.
[0021] Figure 2 shows a second embodiment of the invention. The aqueous solution from the
absorber 110 is passed through line 116 to a modified extractive distillation column
150. Solvent water is introduced to the top of this column through line 152 to absorb
the acetonitrile. Acrylonitrile and HCN is removed overhead as a vapor through line
154. A liquid stream containing acetonitrile and water is removed from the bottom
half of this column through line 158 and sent to a small stripping column 160. Acetonitrile
passes overhead as a vapor through line 162. A liquid stream containing mostly water
is removed from the bottom of column 160 through line 164 and returned to the extractive
distillation column. The present invention's vapor stream is removed from below the
first tray of the distillation column through line 166 and condensed in condenser
168. The condensed stream containing mostly water is then passed through line 170
to waste treatment as described above.
[0022] A bottoms stream containing water, polymers and impurities is removed through line
156 and sent back to the quench system. Additionally, a liquid stream may be removed
from the bottommost trays and returned to the extractive distillation column as solvent
water through ine 152.
Comparative Example A and Example 1
[0023] An acrylonitrile recovery process is performed substantially as shown in Figure 2.
In Comparative Example A the total liquid bottoms stream from the extractive distillation
column is sent to the quench system. Example 1 is identical to Comparative Example
A except that a vapor stream is removed from below the first tray of the extractive
distillation column. The amount of this vapor stream was equal to 45% by weight of
the original bottoms stream in Comparative Example A. Because of this vapor removal,
the amount of heat necessary to perform the distillation was increased by 12%. The
Table below shows the weight percent polymer contained in the various process streams
of both examples.

[0024] As can be seen in this Table, the vapor stream removed from the distillation column
contains extremely small amounts of polymer. The effects of the present invention
can easily be seen by the dramatic increase in polymer concentration in the quench
bottoms stream. This concentration of polymer has been doubled through the use of
the invention. Additionally, the quench bottoms stream is reduced by approximately
60%. Thus a much smaller stream more highly concentrated in polymer is obtained. This
has the advantage of greatly reducing the cost and further disposal of this stream.
[0025] The amount of vapors that may be removed when using the present invention is related
to the bottom stream of the column. The amount of vapors removed can be 10 to about
70 weight percent of the bottoms stream prior to vapor removal. It is preferred, however,
that 30-50 weight percent be removed. This will leave a sufficient quantity of water
for use in the quench system.
[0026] 
[0027] The use of the present invention greatly reduces the amount of quench bottoms to
be purified and also increases its polymer concentration. This makes waste treatment
of this stream far more economical and reduces the size of the associated equipment.
1. A process for the recovery and purification of acrylonitrile or methacrylonitrile
produced by the ammoxidation reaction of propylene or isobutylene, molecular oxygen
and ammonia in the presence of ammoxidation catalysts, comprising:
a) contacting the ammoxidation reactor effluent containing acrylonitrile or methacrylonitrile,
acetonitrile, and impurities with an aqueous quench liquid in a quench system to produce
a gaseous quench effluent from said quench system;
b) absorbing said gaseous quench effluent in water to form an aqueous solution;
c) feeding the aqueous solution to an intermediate tray of a distillation column having
a plurality of trays, using solvent water introduced in the top of said column to
perform a water extractive distillation, wherein an overhead vapor stream of acrylonitrile
or nethacrylonitrile with some water is removed from the top of the column, and a
liquid stream containing water and impurities is removed from the bottom of the column.
d) removing a first sidestream from the lower half of said column to recover acetonitrile;
e) feeding at least a part of the liquid bottoms from said column to the quench system
as quench liquid, characterized by removing a vapor stream containing water from the
lower fourth of said column.
2. A process according to claim 1, characterized in that the vapor stream is removed
from below the first tray of said column.
3. A process according to claims 1 or 2, characterized in that the vapor stream is
condensed after being removed from said column.
4. A process according to anyone of claims 1 to 3, characterized by including the
step of removing a second liquid stream from the lower fourth of said column and using
said second stream as the solvent water to the column.
5. A process according to anyone of claims 1 to 4,

overhead vapor stream of acetonitrile and water from the top of the second column,
and a second liquid stream containing water and impurities from the bottom of the
second column, feeding at least part of the second liquid bottoms stream to the quench
system of (a) as the aqueous quench liquid, and removing a vapor stream from the lower
fourth of said second column.
6. A process according to claim 5, characterized in that the vapor stream is removed
from below the first tray of said second column.
7. A process according to claim 6, characterized in that the vapor stream is condensed
after being removed from the second column.
8. A process according to claim 6, characterized by "including the step of removing a liquid stream from the lower fourth of the second
column and using this stream as the solvent water to the first column in said step
(a).
9. A process according to anyone of the preceding claims,characterized in that the
amount of the vapor stream removed is 10 to about 70 weight percent of the liquid
stream of step (c).
10. A process according to claim 9, characterized in that the amount of the vapor
stream removed is 30 to about 50 weight percent of the liquid stream of step (c).
11. A process according to claims 4 or 8, characterized in that the amount of the
vapor stream removed is 10 to about 70 weight percent of the second liquid stream
of step (d).
12. A process according to claim 11, characterized in that the amount of the vapor
stream removed is 30 to about 50 weight percent of the second liquid stream of step
(d).