U.S. patent application number 11/715776 was filed with the patent office on 2008-07-03 for transesterification process of methyl acetate.
This patent application is currently assigned to National Taiwan University. Invention is credited to Jyun-Hong Chen, Jian-Kai Cheng, Hsiao-Ping Huang, Ming-Jer Lee, Cheng-Ching Yu.
Application Number | 20080161595 11/715776 |
Document ID | / |
Family ID | 39584944 |
Filed Date | 2008-07-03 |
United States Patent
Application |
20080161595 |
Kind Code |
A1 |
Huang; Hsiao-Ping ; et
al. |
July 3, 2008 |
TRANSESTERIFICATION PROCESS OF METHYL ACETATE
Abstract
A transesterification process of methyl acetate is provided. The
process comprises: (a) performing a first reactive distillation of
a methyl acetate solution and a first alcohol to generate a first
ester and a first mixture; (b) performing a first distillation of a
first part of the first mixture to generate a second mixture; and
(c) performing a second reactive distillation of a first part of
the second mixture and a second alcohol to generate a second ester;
wherein the respective one of the first and second alcohols is a
limiting reagent. The transesterification process provided in the
present invention could highly reduce the investing production cost
of the transesterification of the by-product, methyl acetate, in
the conventional polyvinyl alcohol plants.
Inventors: |
Huang; Hsiao-Ping; (Taipei
City, TW) ; Yu; Cheng-Ching; (Taipei City, TW)
; Lee; Ming-Jer; (Taipei City, TW) ; Chen;
Jyun-Hong; (Taipei City, TW) ; Cheng; Jian-Kai;
(Changhua County, TW) |
Correspondence
Address: |
VOLPE AND KOENIG, P.C.
UNITED PLAZA, SUITE 1600, 30 SOUTH 17TH STREET
PHILADELPHIA
PA
19103
US
|
Assignee: |
National Taiwan University
Taipei
TW
|
Family ID: |
39584944 |
Appl. No.: |
11/715776 |
Filed: |
March 8, 2007 |
Current U.S.
Class: |
560/129 |
Current CPC
Class: |
C07C 67/03 20130101;
Y02P 20/10 20151101; C07C 67/54 20130101; Y02P 20/127 20151101;
C07C 67/03 20130101; C07C 69/003 20130101; C07C 67/03 20130101;
C07C 69/14 20130101; C07C 67/54 20130101; C07C 69/14 20130101; C07C
67/54 20130101; C07C 69/003 20130101 |
Class at
Publication: |
560/129 |
International
Class: |
C07C 67/02 20060101
C07C067/02 |
Foreign Application Data
Date |
Code |
Application Number |
Dec 29, 2006 |
TW |
095150090 |
Claims
1. A transesterification process of a methyl acetate, comprising:
(a) performing a first reactive distillation of a methyl acetate
solution and a first alcohol to generate a first ester and a first
mixture; (b) performing a first distillation of a first part of the
first mixture to generate a second mixture; (c) performing a second
reactive distillation of a first part of the second mixture and a
second alcohol to generate a second ester; (d) performing a third
reactive distillation of a second part of the first mixture and a
third alcohol to generate a third ester, wherein the respective one
of the first and second alcohols is a limiting reagent.
2. A process as claimed in claim 1, wherein the methyl acetate
solution includes a 40 mol % methanol.
3. A process as claimed in claim 1, wherein the respective reactive
distillation is operated in a temperature ranged from 55.degree. C.
to [[170 .degree. C.]]170.degree. C. and the step (b) is operated
in a temperature ranged from [[55 .degree. C.]]55.degree. C. to
[[65 .degree. C.] 65.degree. C.
4. A process as claimed in claim 1, wherein the respective reactive
distillation and the distillation are operated in a pressure ranged
from 1 to 2 atmosphere pressure.
5. (canceled)
6. A process as claimed in claim 1, wherein the first, second and
third alcohols are ones selected from a group consisting of an
ethanol, an isopropanol, a propanol, an isobutanol, a butanol, an
isoamyl alcohol, an amyl alcohol, and a hexyl alcohol, and the
first, second and third esters are the same ester.
7. A process as claimed in claim 1, wherein the step (b) further
comprises generating a first methanol therefrom and a step of:
performing a second distillation of a second part of the second
mixture to generate a second methanol.
8. A transesterification process of a methyl acetate, comprising:
(a) reacting a methyl acetate solution with a first alcohol in a
reactive distillation device to generate a first mixture and a
first ester; (b) performing a first distillation of a first part of
the first mixture in a distillation device to generate a second
mixture; (c) refluxing a second part of the first mixture to the
reactive distillation device for a reactive distillation reaction
with a third alcohol, (d) reacting a first part of the second
mixture and a second alcohol in the reactive distillation device to
generate a second ester, wherein the respective one of the first
and the second alcohols is a limiting reagent.
9. (canceled)
10. A process as claimed in claim 10, wherein the first, second and
third alcohols are ones selected from a group consisting of an
ethanol, an isopropanol, a propanol, an isobutanol, a butanol, an
isoamyl alcohol, an amyl alcohol, and a hexyl alcohol, and the
first and the second esters are the same ester.
11. A process as claimed in claim 8, wherein the step (b) further
comprises generating a first methanol and the step (d) further
comprises a step of: performing a second distillation of a second
part of the second mixture to generate a second methanol.
12. A process as claimed in claim 8, wherein the reactive
distillation device comprises a plurality of reactive trays, a
plurality of stripping trays and a plurality of rectifying trays, a
number of the plurality of reactive trays is ranged from 15 to 55,
a number of the plurality of stripping trays is ranged from 3 to
10, and a number of the plurality of rectifying trays is ranged
from 5 to 20.
13. A process as claimed in claim 8, wherein the alcohols are fed
from an upper portion of the reactive distillation device and the
methyl acetate solution is fed from a portion being positioned from
a middle portion to a lower portion of the reactive distillation
device.
14. A transesterification process of a methyl acetate, comprising:
(a) performing a first distillation of a methyl acetate solution to
generate a first methanol and a first mixture; (b) performing a
first reactive distillation of a first part of the first mixture
and a first alcohol to generate a first ester and a second mixture;
(c) performing a second distillation of a first part of the second
mixture to generate a second methanol: and (d) performing a third
distillation of a second part of the first mixture to generate a
third methanol, wherein the first alcohol is a limiting
reagent.
15. (canceled)
16. A process as claimed in claim 14, further comprising a step of:
(e) performing a second reactive distillation of a second part of
the second mixture and a second alcohol to generate a second
ester.
17. A process as claimed in claim 16, wherein the first and second
alcohols are ones selected from a group consisting of an ethanol,
an isopropanol, a propanol, an isobutanol, a butanol, an isoamyl
alcohol, an amyl alcohol, and a hexyl alcohol, and the first and
the second esters are the same ester.
18. A process as claimed in claim 16, wherein the first and the
second reactive distillations are performed in a reactive
distillation device.
19. A process as claimed in claim 18, wherein the alcohols are fed
from an upper portion of the reactive distillation device and the
methyl acetate solution is fed from an upper portion of the
distillation device.
20. A process as claimed in claim 19, wherein the reactive
distillation device comprises a plurality of reactive trays, a
plurality of stripping trays and a plurality of rectifying trays,
and a number of the plurality of reactive trays is ranged from 15
to 55, a number of the plurality of stripping trays is ranged from
3 to 10, and a number of the plurality of rectifying trays is
ranged from 5 to 20.
Description
FIELD OF THE INVENTION
[0001] The present invention relates to a transesterification
process, and more particularly to a transesterification process of
methyl acetate.
BACKGROUND OF THE INVENTION
[0002] Polyvinyl alcohol is a kind of polymer widely used in the
chemical industry; however, the manufacturing process of polyvinyl
alcohol is always accompanying with the abundant production of the
by-product, methyl acetate. Methyl acetate is a less valuable
solvent due to its low industrial application and low volatility,
even if the amount of the produced methyl acetate is one-half times
higher than that of polyvinyl alcohol. Accordingly, the impure
methyl acetate is usually discharged into the atmosphere after
scrubbing in a wastewater treatment system or burned in an
incinerator. In view of the above, if methyl acetate could be
recycled to be efficiently transesterified into other kinds of
esters having higher economical value, the working performance of
the polyvinyl alcohol plants will be highly increased. In recent
years, the transesterification processes of methyl acetate have
been developed as below.
[0003] (1) Luyben et al (2004) proposed one transesterification
process of methyl acetate. The transesterification process was
performed by combination of a reactive distillation tower, a
conventional distillation tower and a distillation tower of high
pressure. Firstly, the conventional distillation tower has two
feeding stream of methyl acetate; one is the mixture of methyl
acetate and methanol, and the other is the reflux stream of the
abundant methanol and methyl acetate from the top of the reactive
distillation tower. The conventional distillation tower functions
as separating methyl acetate from methanol. Methanol could be thus
obtained from the bottom of the conventional distillation tower,
whereas the azeotrope of methyl acetate and methanol could be
formed on the top thereof.
[0004] The reactive distillation tower has also two feeding stream;
one is the azeotrope, and the other is the reflux stream from the
top of the distillation tower of high pressure, where the major
composition of the stream is n-butanol. While the reflux of
n-butanol is fed into the reactive distillation tower, another
substream of fresh n-butanol is mixed simultaneously therewith to
transfer into the upper portion of the reactive section in the
reactive distillation tower, so that methyl acetate and n-butanol
will react therein. Subsequently, one mixture of the abundant
methanol and methyl acetate would be formed on the top of the
reactive distillation tower, and then the mixture would be further
refluxed into the conventional distillation tower to separate
methyl acetate from methanol. Simultaneously, another mixture of
n-butanol and butyl acetate would be obtained from the bottom of
the reactive distillation tower, and the mixture is further
introduced into the distillation tower of high pressure to separate
n-butyl ester from butyl acetate.
[0005] The distillation tower of high pressure could break through
the co-boiling point of n-butyl ester and butyl acetate by means of
applying high pressure. Accordingly, the n-butanol could be formed
on the bottom of the distillation tower of high pressure, whereas
the substantial n-butanol is obtained from the top thereof,
followed by refluxing the substantial n-butanol to the reactive
distillation tower. Though the transerterification process of
methyl acetate proposed by Luyben et al overcomes the co-boiling
phenomenon of n-butyl ester and butyl acetate by means of the
distillation tower of high pressure, the consumption of the steam
amount of the distillation tower of high pressure brings about the
considerable investing production cost to the conventional
polyvinyl alcohol plants.
[0006] (2) Steinigeweg et al (2004) also proposed another
transesterification process of methyl acetate. The process was
performed by combination of a reactive distillation tower, a
conventional distillation tower and a pervaporation device. The
reactive distillation tower has two feeding streams; one is methyl
acetate introduced from the lower portion of the reactive section
thereof, and the other is n-butanol introduced from the upper
portion of the reactive section thereof. Accordingly, the
transesterified product, butyl acetate, would be obtained from the
bottom of the reactive distillation tower and the mixture of methyl
acetate and methanol would be formed on the top thereof.
[0007] Subsequently, the mixture is further introduced to the
pervaporation device. By means of the pervaporation device, methyl
acetate and methanol could be separated and respectively obtained
with high purity. The separated methyl acetate with high purity as
well as another fresh feeding stream of methyl acetate would be
mixed and then introduced into the lower portion of the reactive
section of the reactive distillation tower. Simultaneously, the
separated methanol with high purity is introduced into the
conventional distillation tower for a further separation, wherein
the conventional distillation tower, methanol will be desposited on
the bottom thereof, whereas the azeotrope of methyl acetate and
methanol is formed on the top thereof. Then, the azeotrope is
refluxed to the pervaporation device for a further separation of
methyl acetate and methanol.
[0008] Though the transesterification process proposed by
Steinigeweg et al overcomes the co-boiling phenomenon of methyl
acetate and methanol by means of the pervaporation device, the
regular placement of the film in the pervaporation device also
lowers down the overall economic efficiency of the conventional
polyvinyl alcohol plants.
[0009] In view of the mentioned drawbacks, a special
transesterification process of methyl acetate with the competitive
investing production costs and the higher conversion rate of methyl
acetate is necessary for most polyvinyl alcohol plants.
[0010] From the above description, it is known that how to develop
an efficient and economical transesterification process of methyl
acetate has become a major problem to be solved. In order to
overcome the drawbacks in the prior art, an improved
transesterification process of methyl acetate is provided. The
particular design in the present invention not only solves the
problems described above, but also is easy to be implemented. Thus,
the invention has the utility for the industry.
SUMMARY OF THE INVENTION
[0011] In consideration of a transesterification process of methyl
acetate working in the polyvinyl alcohol plants with a more
economic and efficient operation, a cost-saving transesetrification
of methyl acetate is needed.
[0012] In accordance with one aspect of the present invention, a
transesterification process of methyl acetate is provided, which
comprises the following steps: (a) performing a first reactive
distillation of a methyl acetate solution and a first alcohol to
generate a first ester and a first mixture; (b) performing a first
distillation of a first part of the first mixture to generate a
second mixture; and (c) performing a second reactive distillation
of a first part of the second mixture and a second alcohol to
generate a second ester, wherein the respective one of the first
and second alcohols is a limiting reagent.
[0013] Preferably, the methyl acetate solution includes a 40 mol %
methanol.
[0014] Preferably, the respective reactive distillation is operated
in a temperature ranged from 55.degree. C. to 170.degree. C. and
the step (b) is operated in a temperature ranged from 55.degree. C.
to 65.degree. C.
[0015] Preferably, the respective reactive distillation and the
distillation are operated in a pressure ranged from 1 to 2
atmosphere pressure.
[0016] Preferably, the step (b) further comprises a step of
performing a third reactive distillation of a second part of the
first mixture and a third alcohol to generate a third ester.
[0017] Preferably, the first, second and third alcohols are ones
selected from a group consisting of an ethanol, an isopropanol, a
propanol, an isobutanol, a butanol, an isoamyl alcohol, an amyl
alcohol, and a hexyl alcohol, and the first, second and third
esters are the same ester.
[0018] Preferably, the step (b) further comprises generating a
first methanol therefrom and a step of performing a second
distillation of a second part of the second mixture to generate a
second methanol. In accordance with another aspect of the present
invention, a further transesterification process of methyl acetate
is provided, which comprises the following steps: (a) reacting a
methyl acetate solution with a first alcohol in a reactive
distillation device to generate a first mixture and a first ester;
(b) performing a first distillation of a first part of the first
mixture in a distillation device to generate a second mixture; and
(c) reacting a first part of the second mixture and a second
alcohol in the reactive distillation device to generate a second
ester, wherein the respective one of the first and the second
alcohols is a limiting reagent.
[0019] Preferably, the reactive distillation device comprises a
plurality of reactive trays, a plurality of stripping trays and a
plurality of rectifying trays, and a number of the plurality of
reactive trays is ranged from 15 to 55, a number of the plurality
of stripping trays is ranged from 3 to 10, and a number of the
plurality of rectifying trays is ranged from 5 to 20.
[0020] Preferably, the alcohols are fed from an upper portion of
the reactive distillation device and the methyl acetate solution is
fed from a portion being positioned from a middle portion to a
lower portion of the reactive distillation device.
[0021] In accordance with a further aspect of the present
invention, another transesterification process of methyl acetate is
provided, which comprises the following steps: (a) performing a
first distillation of a methyl acetate solution to generate a first
methanol and a first mixture; (b) performing a first reactive
distillation of a first part of the first mixture and a first
alcohol to generate a first ester and a second mixture; and (c)
performing a second distillation of a first part of the second
mixture to generate a second methanol, wherein the first alcohol is
a limiting reagent.
[0022] Preferably, the step (b) further comprises a step of
performing a third distillation of a second part of the first
mixture to generate a third methanol.
[0023] Preferably, the process further comprises a step of (d)
performing a second reactive distillation of a second part of the
second mixture and a second alcohol to generate a second ester.
[0024] Preferably, the first and second alcohols are ones selected
from a group consisting of an ethanol, an isopropanol, a propanol,
an isobutanol, a butanol, an isoamyl alcohol, an amyl alcohol, and
a hexyl alcohol, and the first and the second esters are the same
ester.
[0025] Preferably, the first and the second reactive distillations
are performed in a reactive distillation device.
[0026] Preferably, the alcohols are fed from an upper portion of
the reactive distillation device and the methyl acetate solution is
fed from an upper portion of the distillation device.
[0027] The above aspects and advantages of the present invention
will become more readily apparent to those ordinarily skilled in
the art after reviewing the following detailed descriptions and
accompanying drawings, in which:
BRIEF DESCRIPTION OF THE DRAWINGS
[0028] FIG. 1(a) is a schematic diagram of the transesterification
process of methyl acetate according to a preferred embodiment of
the present invention.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
[0029] The present invention will now be described more
specifically with reference to the following embodiments. It is to
be noted that the following descriptions of preferred embodiments
of the present invention are presented herein for the purposes of
illustration and description only; it is not intended to be
exhaustive or to be limited to the precise form disclosed.
[0030] A reaction formula of the transesterification reaction of
methyl acetate is shown below:
MeAc+AlcoholMeOH+Ester
[0031] The mentioned abbreviation "MeAc" represents methyl acetate
and the abbreviation "MeOH" represents methanol.
[0032] The transesterification reaction of methyl acetate is a
reversible reaction and possesses the low equilibrium constant. The
feeding of methyl acetate is regarded as a controlling limited
factor in the transesterification reaction of methyl acetate of the
present invention, and thus the reaction will be towards the
generation of the transesterified product. Accordingly, it is
preferred to feed the excess amount of methyl acetate to promote
the reaction towards the generation of the transesterified
product.
[0033] In consideration of the physical properties of the
transesterification system of methyl acetate into butyl acetate in
its entirety, the priority of the boiling points of each
constituent existing therein is shown in Table (1).
TABLE-US-00001 TABLE 1 Constituents Boiling Point (.degree. C.)
Methyl acetate/Methanol 53.57 Methyl acetate 57.05 Methanol 64.53
n-Butanol/Butyl acetate 116.9 n-Butanol 117.7 Butyl acetate
126.0
[0034] In the transesterification system of methyl acetate into
butyl acetate, methyl acetate will react with n-butanol to generate
methanol and butyl acetate. In such transesterification system, the
possible azeotropes include two binary-components, methyl acetate
and methanol together with butyl acetate and n-butanol.
Furthermore, methyl acetate is the lightest component and easily
tends to form the azeotrope with methanol.
[0035] The catalysts required for the transesterification reaction
could be one of the heterogeneous catalysts and homogeneous
catalysts. In the transesterification process of methyl acetate of
the present invention, heterogeneous solid catalysts are utilized
to promote the reaction. The solid catalysts superiors in the
convenience that they be packed anywhere within the reactor (e.g.
the bottom and the top thereof, the reflux device, etc.), so that
the reaction section could be selected flexibly to be disposed
within the reactor, and the problem to recycle the liquid catalyst
could be solved accordingly.
[0036] Ion exchange resins are generally chosen as the solid
catalysts, such as Amberlyst.RTM. 15 (Rohm and Hass) or Purolite
CT179 (Purolite) commonly used in the industry. In addition,
Katapak-S is commonly adopted as the packing structure of the solid
catalysts or the packings of the solid catalysts are disposed
within the trays via a fixed device (Davy Process Technology).
[0037] Please refer to FIG. 1, which depicts a schematic diagram of
the transesterification process of methyl acetate according to a
preferred embodiment of the present invention. The major components
for performing the transesterification process of methyl acetate
are a reactive distillation system, a reflux system, and a
distillation system.
[0038] The reactive distillation system comprises a reactive
distillation device (1), input pipes (I1-I3, and I5), an output
pipe (O1) and another output pipe (O2). The reactive distillation
device (1) is disposed with a rectifying section (1a), a reactive
section (1b) and a stripping section (1c), wherein the rectifying
section (1a) is further disposed with a plurality of rectifying
trays, the reactive section (1b) is disposed with a plurality of
reactive trays, and the stripping area (1c) is disposed with a
plurality of stripping trays. The plurality of reactive trays (1b)
are packed with ion exchange resins (Amberlist.RTM. 15) for
increasing the reaction efficiency.
[0039] An alcohol solution (the n-butanol solution is exemplified
in the following detailed description) from an alcohol solution
tank (B) is fed into an upper portion of the reactive section (1b)
of the reactive distillation device (1) via the input pipe (I2). A
methyl acetate solution is fed into a lower portion of the reactive
section (1b) via the input pipe (I3). Therefore, the n-butanol
solution and the methyl acetate solution will proceed a
transesterification reaction in the reactive section (1b), where
the transesterified product, butyl acetate, will be deposited on
the bottom of the reactive distillation device due to its highest
boiling point in the transesterification system.
[0040] Furthermore, a re-boiling device (6) is disposed beneath the
bottom of the reactive distillation device (1) to heat the butyl
acetate liquid deposited on the bottom of the reactive distillation
device (1), which promotes a further separation of other residues
existing in the butyl acetate liquid.
[0041] The reactive distillation device (1) allows the methyl
acetate solution and the n-butanol solution to perform the
transesterification reaction, and thus the existing components in
the reactive distillation device (1) theoretically include methyl
acetate, n-butanol, methanol and butyl acetate after the
transesterification. However, n-butanol is controlled as the
limiting reagent so it could easily consumed completely and
immediately. Since the boiling point of butyl acetate is highest,
the continuous heating process operated by the re-boiling device
(6) make methyl acetate and methanol of the lower boiling point
convert from a liquid phase to a gaseous one whereby the gaseous
methyl acetate and methanol will rise to the top of the reactive
distillation device (1). Consequently, the ester product, butyl
acetate, will be deposited on the bottom of the reactive
distillation device (1) and obtained in high purity. Then, butyl
acetate is discharged from the output pipe (O2) through a pump (7)
to an ester reservoir (D). The mixture formed by methanol and the
unreacted methyl acetate on the top of the reactive distillation
device (1) is named as a first mixture herein.
[0042] The reactive distillation system in the present invention
further comprises a first condensing system. The first condensing
system comprises a condenser (2) and the relevant connecting tubes,
where the condenser (2) is coupled to the reactive distillation
device (1), so as to liquefy the first mixture from the reactive
distillation device (1).
[0043] The reflux system in the transesterification process of
methyl acetate of the present invention comprises a reflux device
(3), a pump (4), a T-type bypassing tube (5), an input pipe (14),
and an output pipe (O3). The first mixture is discharged from the
output pipe (O1) of the reactive distillation device (1), followed
by being liquefied in the condenser (2), and then fed to the reflux
device (3) via the input pipe (I4). The reflux device (3) is
respectively coupled to the condenser (2) and the T-type bypassing
tube (5). The liquefied fist mixture proceeds a refluxation in the
reflux device (3), and then is discharged via the output pipe (O3)
by the pump (4) to the T-type bypassing device (5). The T-type
bypassing device (5) bypasses a first portion of the refluxed first
mixture into the distillation device (8), which the major
composition of the first portion is methanol, and bypasses a second
portion of the refluxed first mixture into the reactive
distillation device (1), which the major composition of the first
portion is methyl acetate, for continuously proceeding a further
transesterification.
[0044] The distillation system in the transesterification process
of methyl acetate comprises a distillation device (8), the input
pipe (I'1), an input pipe (I6), another input pipe (I8), an output
(O4) and another output pipe (O5). The first portion of the first
mixture is introduced to the distillation device (8) via the input
pipe (I6) for a further distillation.
[0045] Moreover, a re-boiling device (12) is disposed beneath the
bottom of the distillation device (8) to heat the liquid deposited
thereon. As the boiling point of methanol is higher than that of
methyl acetate, the continuous heating process operated by the
re-boiling device (12) makes the methyl acetate in the first
portion of the first mixture convert from a liquid phase to a
gaseous one, and thus the gaseous methyl acetate rise to the top of
the distillation device (8). Such process makes the methanol
solution deposited on the bottom of the distillation device (8)
achieve a higher purity continuously. Then, the methanol solution
of higher purity is discharged via the output pipe (O5) by the pump
(13) and followed by sending to a methanol reservoir (C). The
compositions of the gaseous mixture risen to the top of the
distillation device (8) are respectively butyl acetate and
n-butanol in a rare amount together with methanol and water in a
higher amount, where the gaseous mixture is named as a second
mixture herein.
[0046] The methyl acetate solution is fed to the reactive
distillation device (1) via the input pipe (I1) from a methyl
acetate solution tank (A) or alternatively fed to the distillation
device (8) via the input pipe (I1').
[0047] The transesterification process of methyl acetate in the
present invention further comprises a second condensing system. The
second condensing system comprises a condenser (9) and the relevant
connecting tubes, where the condenser (9) is coupled to the
distillation device (8), so as to liquefy the second mixture from
the distillation device (8).
[0048] Furthermore, the transesterification process of methyl
acetate in the present invention further comprises another reflux
system. The reflux system comprises a reflux device (10), a T-type
bypassing device (14), a pump (11), an input pipe (I7) and an
output pipe (O6). The reflux device (10) is coupled both to the
condenser (9) and the T-type bypassing device (14). Subsequently,
the second mixture on the distillation device (8) is sent to the
reflux device (10), so that the second mixture is liquefied in the
condenser (9), followed by sending to the reflux device (10) via
the input pipe (I7). After the refluxation, the liquefied second
mixture in the reflux device (10) is discharged via the output pipe
(O6) by the pump (11) and then sent to the T-type bypassing tube
(14). The T-type bypassing device (14) further bypasses the second
mixture into two portions, the first portion and the second
portion. Since all the reactions in the present invention occur in
liquid phases, in order to get a higher conversion rate, the first
portion is sent to one from the middle to the lower portion of the
reactive distillation device (1) for a further conversion, whereas
the second portion is recycled to the distillation device (8) for a
further separation of methanol and methyl acetate.
[0049] The temperature of the different sections in the reactive
distillation device (1) varies with the amount of the feeding
streams and is controlled by the re-boiling device disposed on the
bottom thereof. Similarly, the respective temperatures of the
different sections existing in the distillation device (8) are also
controlled in the same way.
[0050] For saving the investing production cost, in the
transesterification process of methyl acetate of the present
invention, the packed range of the solid catalysts in the reactive
distillation device (1) is either from the top to the middle
portion thereof or from the top to the lower portion thereof. In
the present invention, the utilized catalyst is Amerlyst.RTM. 15
sold by Rohm and Hass.TM. which is commonly used in the
industry.
[0051] According to the preferred embodiments of the present
invention, the operating temperature in the reactive distillation
device (1) is in a range from 55.degree. C. to 170.degree. C.
Besides, the operating temperature in the distillation device (8)
is in a range from 55.degree. C. to 65.degree. C. Furthermore, the
operating pressure of the reactive distillation device (1) and the
distillation device (8) is in a range from 1 to 2 atmosphere
pressure, whereas the reflux devices (3) and (10) are operated
under the constant atmosphere pressure.
[0052] In the present invention, the number of the theoretical
trays of the stripping trays in the reactive distillation device
(1) is in a range from 5 to 20, the number of the theoretical trays
of the rectifying trays therein is in a range from 3 to 10, and the
number of the theoretical trays therein is in a ranged from 15 to
55. In addition, the number of the theoretical trays in the
distillation device (8) is in a range from 10 to 25.
EMBODIMENTS
TABLE-US-00002 [0053] Items Embodiment I Embodiment II Mol.
Composition of methyl 60% methyl 60% methyl acetate solution
acetate + acetate + 40% 40% methanol methanol Mol. Composition of
100% n-butanol 100% n-butanol n-butanol solution The reactive
distillation device (1) No. of the reactive trays 35 48 No. of the
rectifying trays 5 5 No. of the stripping trays 8 7 No. of trays
that n-butanol 43th 55th feeds No. of trays that methyl X 12th
acetate feeds No. of trays that a zeotrope feeds 12th 12th The
distillation device (8) No. of total trays 14 19 No. of trays that
methyl 12th X acetate feeds No. of trays that reflux feeds 5th 8th
The amount of reflux 112.45 (kmol/hr) 109.64 (kmol/hr) The purity
of butyl acetate 99 mol % 99 mol % The purity of methanol 99 mol %
99 mol %
[0054] In the Embodiment I, the methyl acetate solution is fed to
the distillation device (8); in the embodiment II, the methyl
acetate solution is fed to the reactive distillation device
(1).
[0055] In conclusion, although the reactive distillation system
depends upon the plurality of reactive trays, the plurality of
stripping trays and the plurality of rectifying trays to serve as
the major reactive sections, they could be alternatively disposed
independently by coupling to the reactive distillation device. As
described above, the working performance disclosed in the present
invention will not be specifically limited to the disclosed
embodiments therein, and all the transesterification process of
methyl acetate by means of the mentioned reactive distillation
system, the reflux system and the distillation system and their
equivalents will not go beyond the protecting scope of the present
invention.
[0056] Therefore, the transesterification process of methyl acetate
in the present invention achieves a more efficient
transesterification without investing considerable production cost,
and is performed by only combination of the reactive distillation
device and the distillation device. The present reactive
distillation device is disposed with three sections, the stripping
section, the reactive section and the rectifying section. The
reactive section is further disposed with a plurality of reactive
trays which packed with solid catalysts. The reactive section is
disposed in a portion being positioned from the upper portion, or
the middle portion to the lower portion within the reactive
distillation device. The rectifying section is disposed upon the
reactive section and the stripping section is disposed
therebeneath. The methyl acetate solution is fed to a portion of
the reactive distillation device being positioned from the middle
portion to the lower portion thereof, or alternatively, fed to a
portion of the distillation device being positioned from the upper
portion to the middle portion thereof. The alcohol reactant is fed
to a portion of the reactive distillation device being positioned
from the upper portion to the middle portion thereof. By reacting
methyl acetate of the excess amount with the alcohol reactants, the
alcohol reactants are almost consumed completely and immediately,
whereby the ester product with high purity could be obtained from
the bottom of the reactive distillation device. Furthermore, the
mixtures formed by methyl acetate and methanol respectively
existing on the top of the reactive distillation and the
distillation device could be liquefied for the subsequent
separation, and the methanol with high purity could be obtained
from the bottom of the distillation device.
[0057] As compared with the transesterification process of methyl
acetate proposed by Luyben et al., the transesterification process
of methyl acetate in the present invention not only reduces the
amount of the required steam and the amount of the catalysts
required to be packed, but also enhances the economic value
thereof.
[0058] Therefore, the present invention proposes an industrially
applicable transesterification process of methyl acetate in
consideration of the thermodynamic properties of the
transesterification system. According to the present invention, an
ester with 99% high purity and a methanol with 99% high purity are
obtained together with low economic costs.
[0059] By virtue of the foregoing, the alcohol reactant could be
ethanol, isopropanol, propanol, isobutanol, butanol, isoamyl
alcohol, amyl alcohol, hexyl alcohol and so on, in the
transesterification process of methyl acetate of the present
invention to satisfy the necessities of the various desired ester
products. By reacting the mentioned alcohols with methyl acetate,
the respective ethyl acetate, isopropyl acetate, propyl acetate,
isobutyl acetate, butyl acetate, isoamyl acetate, amyl acetate,
hexyl acetate and so on, could be obtained. The following will
interpret the present transesterification process of methyl acetate
will be applicable to each of the mentioned alcohols to
transesterify methyl acetate into another ester corresponding to
the selected alcohol.
[0060] Ethanol
[0061] By reacting methyl acetate with ethanol, the ester product,
ethyl acetate is generated correspondingly. In consideration of the
physical properties of the transesterification system of methyl
acetate into ethyl acetate in its entirety, the priority of the
boiling points of each constituent existing therein is shown in
Table (2).
TABLE-US-00003 TABLE 2 Constituents Boiling Point (.degree. C.)
Methanol/Methyl acetate 53.57 Ethanol/Methyl acetate 57.05 Methyl
acetate 57.05 Methanol/Ethyl acetate 62.05 Methanol 64.53
Ethanol/Ethyl acetate 71.81 Ethyl acetate 77.20 Ethanol 78.31
[0062] According to Table (2), the possible azeotropes include four
binary-components, methyl acetate/methanol, methyl acetate/ethanol,
ethyl acetate/methanol and ethyl acetate/ethanol. The boiling point
of the azeotrope formed by methyl acetate and methanol is the
lowest, whereas the boiling point of ethanol is the highest and
that of ethyl acetate is the second highest. However, ethanol is
controlled as the limiting reagent in the transesterification
process so it could be consumed completely and immediately after
feeding without generation of the respective azeotropes, methyl
acetate/ethanol and ethyl acetate/ethanol. Therefore, according to
the transesterification process of methyl acetate in the present
invention, the ethyl acetate of the second highest boiling point
will be formed on the bottom of the reactive distillation device
and obtained in high purity, and the methanol with high purity
could be obtained from the bottom of the distillation system.
[0063] Isoproponal
[0064] By reacting methyl acetate with isopropanol, the ester
product, isopropyl acetate is generated correspondingly. In
consideration of the physical properties of the transesterification
system of methyl acetate into isopropyl acetate in its entirety,
the priority of the boiling points of each constituent existing
therein is shown in Table (3).
TABLE-US-00004 TABLE 3 Constituents Boiling Point (.degree. C.)
Methanol/Methyl acetate 53.57 Methyl acetate 57.05
Methanol/Isopropyl acetate 62.24 Methanol 64.53
Isopropanol/Isopropyl acetate 80.73 Isopropanol 82.35 Isopropyl
acetate 88.52
[0065] According to Table (3), the possible azeotropes include
three binary-components, methyl acetate/methanol, isopropyl
acetate/methanol and isopropyl acetate/isopropanol, wherein methyl
acetate is the lightest component and easily tends to form the
azeotrope with methanol. The azeotrope of methyl acetate and
methanol has the lowest boiling point so it is easily separated
from isopropyl acetate. Furthermore, isopropanol is controlled as
the limiting reagent so it could be consumed completely and
immediately after feeding without generation of the azeotrope of
isopropanol and isopropyl acetate. Regarding the azeotrope of
methanol and isopropyl acetate, their co-boiling point could be
easily broken through by the continuous heating process as well as
the recirculation between the reactive distillation system and the
distillation system. Therefore, according to the
transesterification process of methyl acetate in the present
invention, the isopropyl acetate of the highest boiling point will
be formed on the bottom of the reactive distillation device and
obtained in high purity, and the methanol with high purity could be
obtained from the bottom of the distillation system.
[0066] Propanol
[0067] By reacting methyl acetate with propanol, the ester product,
propyl acetate is generated correspondingly. In consideration of
the physical properties of the transesterification system of methyl
acetate into propyl acetate in its entirety, the priority of the
boiling points of each constituent existing therein is shown in
Table (4).
TABLE-US-00005 TABLE 4 Constituents Boiling Point (.degree. C.)
Methanol/Methyl acetate 53.57 Methyl acetate 57.05 Methanol/Propyl
acetate 62.24 Methanol 64.53 Propanol/Propyl acetate 94.74 Propanol
97.19 Propyl acetate 101.44
[0068] According to Table (4), the possible azeotropes include two
binary-components, methyl acetate/methanol and propyl
acetate/propanol, wherein methyl acetate is the lightest component
and easily tends to form the azeotrope with methanol. The azeotrope
of methyl acetate and methanol has the lowest boiling point so it
is easily separated from propyl acetate. Furthermore, propanol is
controlled as the limiting reagent so it could be consumed
completely and immediately after feeding without generation of the
azeotrope of propanol and propyl acetate. Regarding the azeotrope
of methanol and propyl acetate, their co-boiling point could be
easily broken through by the continuous heating process as well as
the recirculation between the reactive distillation system and the
distillation system. Therefore, according to the
transesterification process of methyl acetate in the present
invention, the propyl acetate of the highest boiling point will be
formed on the bottom of the reactive distillation device and
obtained in high purity, and the methanol with high purity could be
obtained from the bottom of the distillation system.
[0069] Isobutanol
[0070] By reacting methyl acetate with isobutanol, the ester
product, isobutyl acetate is generated correspondingly. In
consideration of the physical properties of the transesterification
system of methyl acetate into isobutyl acetate in its entirety, the
priority of the boiling points of each constituent existing therein
is shown in Table (5).
TABLE-US-00006 TABLE 5 Constituents Boiling Point (.degree. C.)
Methanol/Methyl acetate 53.57 Methyl acetate 57.05
Isobutanol/Isobutyl acetate 98.36 Isobutanol 99.62 Isobutyl acetate
116.40
[0071] According to Table (5), the possible azeotropes include two
binary-components, methyl acetate/methanol and isobutyl
acetate/isobutanol, wherein methyl acetate is the lightest
component and easily tends to form the azeotrope with the methanol.
The azeotrope of methyl acetate and methanol has the lowest boiling
point so it is easily separated from isobutyl acetate. Furthermore,
isobutanol is controlled as the limiting reagent so it could be
consumed completely and immediately after feeding without
generation of the azeotrope of isobutanol and isobutyl acetate.
Therefore, according to the transesterification process of methyl
acetate in the present invention, the isobutyl acetate of the
highest boiling point will be formed on the bottom of the reactive
distillation device and obtained in high purity, and the methanol
with high purity could be obtained from the bottom of the
distillation system.
[0072] Isoamyl Alcohol
[0073] By reacting methyl acetate with isoamyl alcohol, the ester
product, isoamyl acetate is generated correspondingly. In
consideration of the physical properties of the transesterification
system of methyl acetate into isoamyl acetate in its entirety, the
priority of the boiling points of each constituent existing therein
is shown in Table (6).
TABLE-US-00007 TABLE 6 Constituents Boiling Point (.degree. C.)
Methanol/Methyl acetate 53.57 Methyl acetate 57.05 Methanol 64.53
Isoamyl alcohol/Isoamyl 118.90 acetate Isoamyl alcohol 119.01
Isoamyl acetate 141.66
[0074] According to Table (6), the possible azeotropes include two
binary-components, methyl acetate/methanol and isoamyl
acetate/isoamyl alcohol, wherein methyl acetate is the lightest
component and easily tends to form the azeotrope with the methanol.
The azeotrope of methyl acetate and methanol has the lowest boiling
point so it is easily separated from isoamyl acetate. Furthermore,
isoamyl alcohol is controlled as the limiting reagent so it could
be consumed completely and immediately after feeding without
generation of the azeotrope of isoamyl alcohol and isoamyl acetate.
Therefore, according to the transesterification process of methyl
acetate in the present invention, the isoamyl acetate of the
highest boiling point will be formed on the bottom of the reactive
distillation device and obtained in high purity, and the methanol
with high purity could be obtained from the bottom of the
distillation system.
[0075] Amyl Alcohol
[0076] By reacting methyl acetate with amyl alcohol, the ester
product, amyl acetate is generated correspondingly. In
consideration of the physical properties of the transesterification
system of methyl acetate into amyl acetate in its entirety, the
priority of the boiling points of each constituent existing therein
is shown in Table (7).
TABLE-US-00008 TABLE 7 Constituents Boiling Point (.degree. C.)
Methanol/Methyl acetate 53.57 Methyl acetate 57.05 Methanol 64.53
Amyl alcohol 137.68 Amyl acetate 147.71
[0077] According to Table (7), the possible azeotrope only includes
one binary-component, methyl acetate/methanol, wherein methyl
acetate is the lightest component and tends to form the azeotrope
with the methanol. The azeotrope of methyl acetate and methanol has
the lowest boiling point so it is easily separated from amyl
acetate. Furthermore, isoamyl alcohol is controlled as the limiting
reagent so it could be consumed completely and immediately after
feeding. Therefore, according to the transesterification process of
methyl acetate in the present invention, the amyl acetate of the
highest boiling point will be formed on the bottom of the reactive
distillation device and obtained in high purity, and the methanol
with high purity could be obtained from the bottom of the
distillation system.
[0078] Hexyl Alcohol
[0079] By reacting methyl acetate with hexyl alcohol, the ester
product, hexyl acetate is generated correspondingly. In
consideration of the physical properties of the transesterification
system of methyl acetate into hexyl acetate in its entirety, the
priority of the boiling points of each constituent existing therein
is shown in Table (8).
TABLE-US-00009 TABLE 8 Constituents Boiling Point (.degree. C.)
Methanol/Methyl acetate 53.57 Methyl acetate 57.05 Methanol 64.53
Hexyl alcohol/Hexyl acetate 156.60 Hexyl alcohol 157.63 Hexyl
acetate 171.20
[0080] According to Table (8), the possible azeotropes include two
binary-components, methyl acetate/methanol and hexyl acetate/hexyl
alcohol, wherein methyl acetate is the lightest component and
easily tends to form the azeotrope with the methanol. The azeotrope
of methyl acetate and methanol has the lowest boiling point so it
is easily separated from hexyl acetate. Furthermore, hexyl alcohol
is controlled as the limiting reagent so it could be consumed
completely and immediately after feeding without generation of the
azeotrope of hexyl alcohol and hexyl acetate. Therefore, according
to the transesterification process of methyl acetate in the present
invention, the hexyl acetate of the highest boiling point will be
formed on the bottom of the reactive distillation device and
obtained in high purity, and the methanol with high purity could be
obtained from the bottom of the distillation system.
[0081] From the mentioned description, the present
transesterification process of the methyl acetate is capable of
generating the desired ester product by means of selecting the
corresponding alcohol as the reactants. There exists the
consistence in each of the mentioned transesterification system
that the boiling point of the azeotrope formed by methyl acetate
and methanol is the lowest as well as the boiling point of ester
product is the highest. Such consistence is beneficial to the
present transesterification process of the methyl acetate.
Moreover, the present transesterification process of methyl acetate
takes the alcohol reactants as the limiting reagent, which the
alcohol reactant reacts with the methyl acetate of the excess
amount, so that the alcohol reactant is almost completely consumed.
Accordingly, the azeotropes formed by the alcohol reactant almost
fail to be generated, and the ester product of the highest boiling
points will be obtained from the bottom of the reactive
distillation device.
[0082] In view of the above, the transesterification process of
methyl acetate in the present invention is capable of being
applicable to various kinds of alcohols to transesterify methyl
acetate into the corresponding esters. In addition, the
transesterification process provided in the present invention could
highly reduce the investing production cost of the
transesterification of the by-product, methyl acetate, in the
conventional polyvinyl alcohol plants.
[0083] While the invention has been described in terms of what is
presently considered to be the most practical and preferred
embodiments, it is to be understood that the invention needs not be
limited to the disclosed embodiments. On the contrary, it is
intended to cover various modifications and similar arrangements
included within the spirit and scope of the appended claims which
are to be accorded with the broadest interpretation so as to
encompass all such modifications and similar structures.
* * * * *