U.S. patent application number 10/251353 was filed with the patent office on 2003-01-23 for process for removing water from aqueous methanol.
Invention is credited to Gilbert, Benjamin A., Kirkpatrick, Jeffrey R., McCall, John C., Windhorst, Kenneth A..
Application Number | 20030015412 10/251353 |
Document ID | / |
Family ID | 25077465 |
Filed Date | 2003-01-23 |
United States Patent
Application |
20030015412 |
Kind Code |
A1 |
Gilbert, Benjamin A. ; et
al. |
January 23, 2003 |
Process for removing water from aqueous methanol
Abstract
A process for separating water from methanol in an aqueous
methanol initial mixture, comprising subjecting said mixture to
azeotropic distillation in the presence of sufficient added methyl
acrylate to form an azeotrope with most of the methanol in said
initial mixture such that a substantial proportion of methanol in
the initial mixture is removed as an azeotrope of methanol and
methyl acrylate in the overhead vapors resulting from said
distillation and a major proportion of water in said initial
mixture is removed in the liquid residue of said distillation.
Inventors: |
Gilbert, Benjamin A.;
(Pampa, TX) ; Kirkpatrick, Jeffrey R.; (Pampa,
TX) ; McCall, John C.; (Pampa, TX) ;
Windhorst, Kenneth A.; (Portland, TX) |
Correspondence
Address: |
M. Susan Spiering
c/o Celanese Ltd.
P.O. Box 9077
Corpus Christi
TX
78469-9077
US
|
Family ID: |
25077465 |
Appl. No.: |
10/251353 |
Filed: |
September 20, 2002 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
10251353 |
Sep 20, 2002 |
|
|
|
09766765 |
Jan 22, 2001 |
|
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Current U.S.
Class: |
203/18 ;
203/60 |
Current CPC
Class: |
Y10S 203/24 20130101;
C07C 29/82 20130101; C07C 29/82 20130101; C07C 31/04 20130101 |
Class at
Publication: |
203/18 ;
203/60 |
International
Class: |
B01D 003/34; C07C
029/80; B01D 003/00 |
Claims
We claim:
1. A process for separating water from methanol in an aqueous
methanol initial mixture, comprising subjecting said mixture to
azeotropic distillation in the presence of sufficient added methyl
acrylate to form an azeotrope with most of the methanol in said
initial mixture such that a substantial proportion of methanol in
the initial mixture is removed as an azeotrope of methanol and
methyl acrylate in the overhead vapors resulting from said
distillation and a major proportion of water in said initial
mixture is removed in the liquid residue of said distillation.
2. The process of claim 1 wherein said initial mixture contains
about 1 to about 99 wt. % of methanol, and about 99 to about 1 wt.
% of water.
3. The process of claim 2 wherein the methanol is present in the
initial mixture in the range of about 5 to about 10 wt. % and water
is present in the range of about 85 to 95 wt. %.
4. The process of claim 1 wherein the amount of methyl acrylate
added to the system ranges from about 95% of the amount necessary
to form an azeotrope with all the methanol present to about a 20%
excess over the latter amount.
5. The process of claim 4 wherein said amount of methyl acrylate
ranges from about the approximate amount necessary to form an
azeotrope with substantially all the methanol present, to about a
5% excess over the latter amount.
6. The process of claim 1 wherein said azeotropic distillation is
carried out in a fractional distillation tower at an intermediate
point of which is fed the sole or main stream of initial aqueous
methanol feed mixture, the bottom of said tower where said residue
is withdrawn being at a temperature of about 95 to about
100.degree. C., the intermediate point of said tower where said
sole or main stream of the initial aqueous methanol mixture enters
the tower being at a temperature of about 90 to about 95.degree. C.
and the top of the tower where the overhead vapors are removed
being at a temperature of about 60 to about 65.degree. C.
7. The process of claim 1 wherein said overhead vapors are
condensed with most of the condensate being recycled to the
distillation as reflux at a reflux ratio of about 3 to about 10 and
the remainder of the condensate being withdrawn as a product of the
azeotropic distillation with reduced water content.
8. The process of claim 7 wherein said water content of the
condensate is no greater than about 10 wt. %.
9. The process of claim 8 wherein said water content is no greater
than about 3 wt. %.
10. The process of claim 1 wherein the amount of methanol in said
residue is no greater than about 1 000 ppm.
11. The process of claim 10 wherein said amount of methanol is no
greater than about 150 ppm.
12. The process of claim 7 wherein the portion of the condensate
withdrawn as a product of said azeotropic distillation is fed to
the reaction stage of a process for producing methyl acrylate by
esterification of acrylic acid with excess methanol, and methanol
in the reaction product is separated from methyl acrylate by
extraction with water.
13. The process of claim 12 wherein at least a portion of said
aqueous methanol initial mixture fed to said azeotropic
distillation is an aqueous residue obtained from said
extraction.
14. The process of claim 7 wherein a polymerization inhibitor is
added to said condensate.
15. The process of claim 14 wherein said inhibitor is
phenothiazine.
16. The process of claim 6 wherein energy is supplied to said
azeotropic distillation by directly injecting live steam into said
tower.
Description
BACKGROUND OF THE INVENTION
[0001] 1. Field of the Invention
[0002] This invention relates to a process for removing water from
aqueous methanol by azeotropic distillation.
[0003] 2. Description of the Related Art
[0004] Methanol is a widely used industrial chemical used to
synthesize many different compounds and industrial products. In
several processes utilizing methanol as a synthesizing feed
compound, e.g., production of methyl esters, unreacted aqueous
methanol is produced as a by-product which must be treated to
remove water so that methanol of acceptable purity, i.e., having no
more than a certain maximum percentage of water, may be recycled to
the process. A common form of purification for removal of water
from aqueous methanol is fractional distillation. However,
disadvantages of this treatment are that the equipment for carrying
out this treatment has a relatively high capital cost and the
wastewater produced as a residue cannot have more than a certain
proportion of methanol, e.g., about 1000 ppm, in order to meet
environmental regulations. Thus, any expedient which can serve to
keep the equipment and therefore its cost as small as possible, and
the content of methanol in the separated water of the residue as
low as possible, is very desirable.
[0005] U.S. Pat. No. 3,293,154 issued Dec. 20, 1966 to R. H.
Newton, discloses a process in which a methanol-water mixture in
vapor form is contacted with a water-insoluble, normally liquid
hydrocarbon having a boiling point substantially no higher than the
boiling point of methanol, to form an azeotrope with the free
water, which azeotrope has a boiling point sufficiently different
from that of methanol to accomplish the separation of enough water
from the methanol to produce an essentially anhydrous alcohol.
[0006] U.S. Pat. No. 3,686,268, issued Aug. 22, 1972 to Jobert et.
al., teaches a process for the manufacture of acrylic or
methacrylic higher esters by transesterification of a first alcohol
with an acrylic or methacrylic ester of a second alcohol having
less carbon atoms than the first alcohol in the presence of a
titanium phenoxide catalyst, and drawing off the second alcohol by
azeotropic distillation with the ester of the second alcohol.
[0007] U.S. Pat. No. 3,875,212, issued Apr. 16, 1975 to Ohrui et.
al., discloses a process for the synthesis of an acrylic ester such
as methyl acrylate by esterifying acrylic acid with methanol or
ethanol in the presence of a water-insoluble hydrocarbon solvent
while azeotropically boiling water formed in the esterification
together with the solvent and distilling the ester simultaneously;
and separating the resulting effluent esterification solution into
an organic solvent layer and an aqueous layer by decantation.
[0008] U.S. Pat. No. 4,076,950, issued Feb. 28, 1978 to Stewart et.
al., teaches a continuous process for the preparation of acrylic
and methacrylic esters such as methyl acrylate, in which
substantially anhydrous product ester is added to the reactor to
satisfy the ester/alkanol and ester/water azeotropes thereby
removing crude product ester, unreacted alkanol and water of
esterification from the esterification reactor while leaving
substantially all the high boiling acrylic or methacrylic acid in
the reactor.
BRIEF SUMMARY OF THE INVENTION
[0009] In accordance with this invention, water is removed from an
initial mixture comprising methanol and water by subjecting said
mixture to azeotropic fractional distillation in the presence of
sufficient added methyl acrylate to form an azeotrope with most of
the methanol in said mixture such that a substantial proportion of
the methanol in the initial mixture is removed as an overhead
azeotrope of methanol and methyl acrylate having an atmospheric
boiling point of 62.5.degree. C. and containing about 46 weight
percent (wt. %) of methyl acrylate and about 54 wt. % of methanol,
with a major proportion of the water in the initial methanol-water
mixture being removed as a residue of the distillation usually
containing a small amount of methanol and no more than a trace of
methyl acrylate.
[0010] The process of this invention is capable of treating aqueous
methanol to obtain a separated water in the residue containing
substantially less methanol, and, in some cases an overhead
containing significantly less water, than that obtained when no
methyl acrylate is added, using similar equipment and energy
expenditure, or such process can be used to treat aqueous methanol
to obtain a separated water residue containing a similar amount of
methanol and an overhead stream containing a comparable percentage
of water, than when no methyl acrylate is added, using smaller
equipment, and/or a lower expenditure of energy. Alternatively, a
combination of these relative advantages may be obtained at various
levels of equipment size, energy expenditure and percentage of
methanol in the residue water.
[0011] It can thus be seen that the process of the invention can
yield a significant economic advantage in the lower cost of
equipment and/or energy and/or an environmental advantage due to a
lower amount of methanol in the residue water if such water is to
be discarded.
BRIEF DESCRIPTION OF THE DRAWING
[0012] The drawing is a schematic diagram of the process of this
invention for separating water from a water-methanol mixture when
the process is used to treat at least one recycle stream from the
purification section of a process for making methyl acrylate by
esterification of acrylic acid with methanol.
DETAILED DESCRIPTION OF THE INVENTION
[0013] The initial aqueous methanol mixture treated to reduce its
percentage of water in accordance with this invention prior to the
addition of methyl acrylate, may contain, for example, about 1 to
about 99 wt. % of methanol, and about 99 to about 1 wt. % of water,
preferably about 5 to about 10 wt. % of methanol and about 85 to
about 95 wt. % of water, all percentages based on the weight of the
total mixture. Relatively small amounts of other compounds may also
be present in the initial aqueous methanol mixture, e.g., methyl
acrylate, particularly if the process of separating water from
methanol in accordance with this invention is employed in
conjunction with methyl acrylate production, to be discussed more
fully hereinafter.
[0014] The amount of methyl acrylate added to the initial aqueous
methanol mixture subjected to the azeotropic distillation may be in
the range, for example, of about 95% of the amount necessary to
form an azeotrope with all the methanol present to about a 20%
excess over the latter amount, preferably from about the
approximate amount necessary to form an azeotrope with
substantially all the methanol present to about a 5% excess over
that amount.
[0015] Because of a low degree of solubility of methyl acrylate in
water, and due to recycle streams, a small amount of methyl
acrylate may be present in the initial aqueous methanol mixture
subjected to azeotropic distillation under steady state conditions
before the addition of methyl acrylate in the amounts described.
This small amount may be larger if the azeotropic distillation
process of the invention is used for the recovery and recycling of
methanol in conjunction with a methyl acrylate production process,
since much of the initial aqueous methanol treated is obtained in
the course of recovering and recycling the portion of the excess
methanol which dissolves in the water of esterification, in which
the methyl acrylate product is also slightly soluble. The amount of
methyl acrylate present in the initial aqueous methanol to be
treated before the addition of methyl acrylate may be, for example,
in the range of about 2 to about 10 wt. % based on the weight of
the mixture, and this amount should be taken into account in
determining how much methyl acrylate should be added to the initial
aqueous methanol mixture to reach the desired amount.
[0016] The aqueous methanol mixture to be treated for the
separation of water in accordance with this invention, may be added
to a fractional distillation tower as a single stream or as more
than one stream, e.g. different recycle streams from various
purification units of a methyl acrylate production process. If more
than one stream enters the tower, then the percentages of methanol,
water and methyl acrylate mentioned previously apply to the total
of all the streams. Furthermore, the added methyl acrylate utilized
to form an azeotrope with methanol during distillation may be added
to the distillation tower as a separate stream, in which case it
should be added below the lowest feed point of aqueous methanol, or
preferably, it may be mixed with an aqueous methanol stream before
it is fed to the distillation tower.
[0017] The distillation may be carried out using a tower of any
conventional design to accomplish fractionation, e.g., containing
sieve trays, baffle plates, or packing. Preferably, sieve trays are
utilized which may number, for example, about 5 to about 20 and
some of which may be slotted. Heat may be supplied to the tower by
any conventional means, e.g., injection of live steam, use of a
steam heated jacket or electrical heating elements. The temperature
in the tower during the separation process may be, for example,
about 95 to about 100.degree. C. near the bottom, where the residue
water is withdrawn; for example, about 90 to about 95.degree. C. at
an intermediate point near where the sole or main stream of initial
aqueous methanol feed mixture enters the tower; and, for example,
about 60 to about 65.degree. C. near the top of the tower from
which point the methyl acrylate azeotrope vapor leaves the tower as
overhead and flows to a condenser/receiver where it is condensed
into a liquid mixture having a composition similar to that of the
methanol/methyl acrylate azeotrope with reduced water content, the
amount of water present being due to the formation of a
water/methyl acrylate azeotrope having an atmospheric boiling point
of 71.degree. C. Most of the condensate is returned to the tower as
reflux using a reflux ratio of, for example, about 3 to about 10,
for the purpose of increasing the separation efficiency of the
azeotropic distillation. That portion of the condensate not
returned to the tower as reflux can be treated to separate the
methanol having a substantially reduced water content from the
methyl acrylate which may be recycled with makeup methyl acrylate
to the azeotropic distillation. The residue from the azeotropic
distillation is primarily water containing a small amount of
methanol preferably no more than about 1000 ppm, more preferably no
more than about 150 ppm. The residue water may be treated to
recover its heat energy and reused in a related process, or it may
be discarded as a waste stream.
[0018] The process of this invention employing azeotropic
distillation to separate water from aqueous methanol is
conveniently combined with a methyl acrylate production process of
the type well known in the art wherein acrylic acid is esterified
with an excess of methanol using an acid catalyst such as sulfuric
acid and yielding a crude product comprising methyl acrylate, water
of esterification and unreacted methanol. Pure methyl acrylate is
obtained by subjecting the crude product to various purification
operations including water extraction from which aqueous methanol
is obtained as a residue suitable as the initial mixture to be fed
to the azeotropic distillation of this invention to recover
methanol having a reduced water content. Such methanol can be
recycled to the methyl acrylate esterification reactor as a mixture
with methyl acrylate, or after having been separated from the
methyl acrylate azeotroping agent. Since the addition of water to
the methyl acrylate esterification reaction tends to reverse the
reaction due to equilibrium considerations, the percentage of water
in the portion of the methanol/methyl acrylate overhead from the
azeotropic distillation being recycled to the exterification
reactor should be as low as possible, e.g., no higher than about 10
wt. %, preferably no higher than about 3 wt. %.
[0019] In carrying out the process of the invention, it is
desirable to add a water-soluble polymerization inhibitor, such as
phenothiazine (PTZ) or hydroquinone to the system to reduce the
formation of methyl acrylate polymers, too much of which causes
fouling of the equipment and prevents the recovery of heat from the
water residue or the reuse of such water residue due to the
presence of such polymers. While the inhibitor may be injected into
any stream in the system including the feed and reflux streams and
the liquid in the overhead condenser-receiver, it has been found
that the most benefit is obtained when the inhibitor is added only
to the overhead condenser/receiver.
[0020] Turning now to the drawing, entering azeotropic distillation
tower 1 are a feed stream of aqueous methanol extractive residues
from the purification section of a methyl acrylate production
process, fed through line 2, to which has been added methyl
acrylate azeotroping agent obtained from the latter purification
section, fed through line 3, a reflux stream comprising methanol,
methyl acrylate and a small amount of water, fed through line 4
which is part of the liquid condensate from condenser/receiver 5,
the aqueous methanol obtained as a heavy phase from a decanter (not
shown) receiving the overhead condensate from the
reactor/fractionating tower (not shown) of a methyl acrylate
production process, fed to tower 1 through line 6, and live stream
to provide heat energy and additional water to tower 1, fed through
line 7. Overhead vapors from tower 1 composed primarily of the
methanol/methyl acrylate azeotrope and a lesser amount of a
water/methyl acrylate azeotrope are withdrawn from tower 1 and flow
to condenser/receiver 5 through line 8. Water containing a small
amount of methanol is withdrawn from tower 1 as a residue through
line 9 and is either treated to recover its heat energy and reused
in the methyl acrylate production process or is sent to waste
treatment. A small amount of a polymerization inhibitor such as
phenothiazine (PTZ) fed to condenser/receiver 5 through line 10,
acts to reduce fouling and decrease the amount of polymer in the
residue water which is desirable if the water is to be reused in
the methyl acrylate process. That portion of the overhead
condensate from condenser/receiver 5 not returned to tower 1 as
reflux is the main product of the process of this invention and is
fed through line 11 to the reactor/fractionating tower of the
methyl acrylate process for reuse in the process.
[0021] The following examples further illustrate the invention.
EXAMPLE 1
[0022] For laboratory modeling of the process of the invention, an
Oldershaw distillation column was employed containing a bottom
reboiler section heated by an electrical element, a 10 tray section
above the reboiler, a feed section above the 10 tray section, a 5
tray section above the feed section, an overhead take-off section
above the 5 tray section and a condenser above the overhead
take-off section. The process was started up by heating a feed
comprising 9.4 wt. % of methyl acrylate, 10.47 wt. % of methanol
and about 80 wt. % of water, which included added methyl acrylate
in an amount of about 5% excess over that necessary to form an
azeotrope with the methanol present. The feed rate was 9.2 g/min
(grams per minute) the residue take off was 7.2 ml/min (milliliters
per minute) and the reflux ratio was 5:1. Readings were taken of
the reboiler temperature (Bottom T), temperature at the feed point
(Feed T), temperature at the overhead take-off point (OH T), all in
degrees Celsius, percentage of water in the overhead (OH
H.sub.2O,%), and parts per million of methanol in the residue (Res.
MeOH, ppm). The system was assumed to be relatively stable when the
residue methanol fell below 1000 ppm and the first set of readings
meeting this condition was considered to be the time zero point
(Time=0). Thereafter, the foregoing readings were taken at various
intervals and recorded opposite the total time elapsed from the
time zero point given in the following table (Time, hrs.).
1TABLE Time, Bottom T Feed T Top T OH H.sub.2O Res. MeOH hrs.
.degree. C. .degree. C. .degree. C. % ppm 0 97.8 94 47.7 2.8 35 0.5
97.8 92.6 49.6 5.4 4.8 1.0 97.6 91.7 54.6 9.9 22 1.5 97.6 90.5 50.0
3.0 26 1.75 97.4 90.3 49.6 2.5 33 2.0 97.4 80 48.8 2.3 55 3.0 97.5
77.4 48.6 3.1 65 3.33 97.4 80.6 48.5 2.6 96 4.0 97.5 72.3 49.0 3.1
235
[0023] The OH H.sub.2O and Res. readings at Time =0.5 and the OH
H.sub.2O reading at Time=1.0 were probably altered by the temporary
malfunction of a reflux valve affecting conditions during those
intervals.
[0024] The overall values shown in the table indicate that the
process of the invention is suitable for the efficient separation
of water from aqueous methanol in which the residue water contains
a particularly small amount of methanol, which is desirable from an
environmental standpoint, while yielding an overhead condensate
containing an acceptably low percentage of water. The remaining
major proportion of the condensate is composed primarily of
methanol and methyl acrylate in proportions close to those of the
azeotrope of these compounds, and which can be separated by methods
known in the art, e.g., water extraction of the methanol.
EXAMPLE 2
[0025] This example is based on the process illustrated in the
drawing as described previously. Azeotropic distillation tower 1
contains 20 sieve trays, trays 6-9 of which are slotted. The
aqueous methanol feed to tower 1 consists of 9.5 MLBH (thousand
pounds per hour) of the extractive residues obtained from the water
extraction of methanol from an overhead stream comprising methanol
and methyl acrylate produced by the esterification of acrylic acid
with methanol in a reactor/distillation tower, such aqueous
residues being fed to tower 1 through line 2, and 1.5 MLBH of the
heavy phase decanted from an overhead stream from the latter
reactor/distillation tower, fed through line 6. To the feed stream
in line 2 is added enough methyl acrylate to provide a 5% excess
over that necessary to completely azeotrope with the methanol
present, fed through line 3. The aqueous methanol and methyl
acrylate fed to tower 1 through lines 2, 3 and 6 results in an
overall feed comprising 8 wt. % of methanol, 6 wt. % of methyl
acrylate, and 86 wt. % of water.
[0026] Also fed to tower 1 through line 7 are 6.0 MLBH of 50 psig
live steam which provide heat energy. During steady state
operation, tower 1 has a bottom temperature of 96.degree. C., an
intermediate temperature of 93.degree. C. near the feed point of
line 2, and a top temperature of 60.degree. C. near the feed point
of line 6. Overhead vapors in an amount of 9.0 MLBL and composed of
51 wt. % of methanol, 47 wt. % of methyl acrylate and 2 wt. % of
water, leave the top of tower 1 through line 8 and are condensed in
condenser/receiver 5, with 7.5 MLBH being recycled back to the top
of tower 1 as reflux, and 1.5 MLBH being withdrawn through line 5
as product, for a reflux ratio of 5:1. The withdrawn product is
recycled to the reactor/distillation tower of the methyl acrylate
production process. A small amount of phenothiazine polymerization
inhibitor is injected into condenser/receiver 5 through line 10. .
Residue water in an amount of 15.0 MLBH and containing 100 ppm of
methanol is withdrawn from the bottom of tower 1 through line 9 as
effluent and is either treated to recover heat energy and reused as
methanol extractant in the separation of methanol from methyl
acrylate or is sent to waste treatment.
* * * * *