GB2069369A - Method and apparatus for removal of heat from an olefin polymerization reactor - Google Patents
Method and apparatus for removal of heat from an olefin polymerization reactor Download PDFInfo
- Publication number
- GB2069369A GB2069369A GB8103699A GB8103699A GB2069369A GB 2069369 A GB2069369 A GB 2069369A GB 8103699 A GB8103699 A GB 8103699A GB 8103699 A GB8103699 A GB 8103699A GB 2069369 A GB2069369 A GB 2069369A
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- GB
- United Kingdom
- Prior art keywords
- polymerization reactor
- reflux condenser
- gas mixture
- washing
- heat
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/0006—Controlling or regulating processes
- B01J19/0013—Controlling the temperature of the process
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00051—Controlling the temperature
- B01J2219/00074—Controlling the temperature by indirect heating or cooling employing heat exchange fluids
- B01J2219/00087—Controlling the temperature by indirect heating or cooling employing heat exchange fluids with heat exchange elements outside the reactor
- B01J2219/00101—Reflux columns
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00164—Controlling or regulating processes controlling the flow
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00184—Controlling or regulating processes controlling the weight of reactants in the reactor vessel
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/04—Monomers containing three or four carbon atoms
- C08F110/06—Propene
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Polymerisation Methods In General (AREA)
Abstract
In polymerizing a C2 to C8 olefin, in a polymerization reactor with a reflux condenser (3), a gas mixture (4) withdrawn from the polymerization reactor is first washed (2) before it in reaches the heat transfer surface of the reflux condenser (3) to remove active catalyst particles and polymer particles entrained therein. It is then partially condensed in the reflux condenser (3) to obtain a condensed liquid (7) for return to the polymerization reactor whereby the heat generated in the polymerization reactor is efficiently removed without causing any clogging of pipes. The uncondensed gas is returned to the reactor via a compressor. The washing means is a gas-liquid contactor such as a tray, disc scrubber or cyclone scrubber, or spray tower and can be in the lower portion of the condenser. The washing is preferably by countercurrent contact of the gas mixture with condensed liquid obtained in the condenser and/or solvent. <IMAGE>
Description
SPECIFICATION
Method and apparatus for removal of heat from an olefin polymerization reactor
This invention relates to an improved method and apparatus for the removal of heat from a polymerization reactor having a reflux condenser which is used for the catalytic polymerization of olefins in a low boiling point hydrocarbon solvent.
Recently, with an increase in the amount of polyolefins being produced, there has been a tendency for polymerization reactors of large volume to be employed or for the amount of polyolefins being produced per polymerization reactor to be increased. For heat removal from the polymerization reactor, therefore, various methods as well as the usual heat removal method using a jacket have been developed, including a method in which an internal cooler (e.g., a plate cooler or d coil cooler) is mounted in the polymerization reactor, and a method in which a reflux condenser is used for the heat removal by circulating a liquid phase portion in the polymerization reactor into an external cooler. Such a method using the reflux condenser is described in British Patent 991,397 and U.S. Patents 3,785,430 and 4,061,848.
The method using the reflux condenser, however, suffers from the disadvantage that when the reflux condenser is continuously used, active catalyst particles and polymer particles, both of which particles are entrained in a gas to be condensed, are deposited on the heat transfer surface of the reflux condenser to form scales, or heavier deposits, which result in a reduction of the heat removal ability. Furthermore, these deposits give rise to various problems, that is to say, when they are locally stripped off, they clog a flow path through which the condensed liquid returns to the polymerization reactor, enter the polymerization reactor to adversely affect the quality of polyolefin products, and clog a conduit through which the liquid phase portion in the polymerization reactor is withdrawn.In order to overcome such problems, it is necessary to wash the heat transfer surface of the reflux condenser at 2 or 3 month intervals.
In order to wash the heat transfer surface, it is necessary to separate the reflux condenser from the polymerization reactor by stopping the polymerization or by extremely reducing the amount of polyolefins being produced. In either case, this leads to a marked reduction in productivity.
An object of this invention is to provide a method and apparatus for heat removal from a polymerization reactor with a reflux condenser, which method permits to substantially or completely prevent the formation of polymer scales on the heat transfer surface of the reflux condenser.
It has now been found that the above object is attained by providing a washing system for washing a gas mixture withdrawn from the polymerization reactor before it reaches the heat transfer surface of the reflux condenser.
This invention, therefore, relates to a method and apparatus for the heat removal from a polymerization reactor with a reflux condenser, in which an unsaturated hydrocarbon monomer having 2 to 8 carbon atoms is polymerized in an inert hydrocarbon or the liquefied monomer having 3 to 8 carbon atoms as a solvent in the presence of an olefin polymerization catalyst, by introducing a gas mixture withdrawn from the polymerization reactor into the reflux condenser where the gas mixture is condensed and separated into a condensed liquid and an uncondensed gas and returning the condensed liquid to the polymerization reactor (by gravity flow or with a pump) and the uncondensed gas into the liquid phase in the polymerization reactor by the use of a compressor, wherein the gas mixture from the polymerization reactor is brought in countercurrent contact with the condensed liquid and/or the solvent to be supplied to the polymerization reactor before the gas mixture reaches the heat transfer surface of the reflux condenser to remove active catalyst particles and polymer particles (both of which particles are entrained in the gas to be condensed).
As a reflux condenser used in practicing this invention, usual multitubular heat exchangers of either the vertical type or horizontal type can be used.
A washing apparatus used in this invention is a usual gas-liquid contactor. Preferred examples are trays such as a sieve tray, a turbogrid tray or a ripple tray, scrubbers such as a pibo disc scrubber or a cyclone scrubber and spray towers.
The reflux condenser and the washing apparatus may be installed separately or combined together to provide a system in which the washing apparatus is contained in the lower portion of the reflux condenser. These embodiments will be hereinafter explained by reference to the accompanying drawings, wherein:
Figures 1 A to 1 F each illustrates a washing system in which a condensed liquid is used as a washing liquid; Figures 2A to 2C each illustrates a combination of a washing system in which a solvent to be supplied to a polymerization reactor is used as a washing liquid and a reflux condenser;
Figure 3 is a flow diagram of a combination of a polymerization reactor and an apparatus for the heat removal from the polymerization reactor; and
Figure 4 is a sectional view of a reflux condenser containing therein a washing system.
In Figures 1 to 4, numeral 1 indicates a polymerization reactor, 2 a washing apparatus, 3 a reflux condenser, 4 piping through which the gas mixture is introduced into the washing apparatus, 5 piping through which the gas mixture withdrawn from the washing apparatus is introduced into the reflux condenser, 6 piping through which the uncondensed gas mixture flows, 7 piping through which the condensed liquid is withdrawn from the reflux condenser, 8 piping through which the liquid is withdrawn from the washing apparatus, 9 piping through which the washing liquid is introduced into the washing apparatus, 10 piping through which the cooling water is supplied, 11 a control valve for cooling water, 12 a heat transfer tube of the condenser, 13 a washing apparatus (tray), 14 a washing apparatus (down comer), 1 5 a compressor for circulating the uncondensed gas mixture and 1 6 a temperature regulator.
Figures 1 A to 1 F each illustrates an embodiment in which the condensed liquid is used as the washing liquid; that is, Figure 1 A shows an embodiment in which a vertical type reflux condenser is combined with an independent washing apparatus; Figure 1 B an embodiment in which a horizontal type reflux condenser is combined with an independent washing apparatus; Figure 1 C an embodiment in which a horizontal type reflux condenser contains therein a washing apparatus; Figure 1 D an embodiment in which a vertical type reflux condenser contains a washing apparatus; Figure 1 E an embodiment in which a vertical type reflux condenser is combined with a washing apparatus directly mounted on a polymerization reactor; and Figure 1 F an embodiment in which a vertical type condenser containing therein a washing apparatus is directly mounted on a polymerization reactor.
Figures 2A to 2C each illustrates an embodiment in which the solvent to be supplied to the polymerization reactor is used as the washing liquid; that is, Figure 2A shows an embodiment in which a vertical type reflux condenser is combined with an independent washing apparatus; Figure 2B an embodiment in which a horizontal type reflux condenser is combined with an independent washing apparatus; and Figure 2C an embodiment in which a vertical type reflux condenser is combined with a washing apparatus directly mounted on a polymerization reactor.
This invention wiil be hereinafter described in greater detail by reference to Figures 3 and 4.
Figure 3 is a flow diagram of a whole heat removal system from a polymerization reactor, and Figure 4 shows a sectional view of a vertical multitubular type reflux condenser containing therein the washing apparatus indicated by 3 in
Figure 3 (corresponding to Figure 1 D).
In the inside of a polymerization reactor 1, an unsaturated hydrocarbon monomer having 2 to 8 carbon atoms, an inert hydrocarbon or the liquefied monomer having 3 to 8 carbon atoms as a solvent, an olefin polymerization catalyst, and, usualiy, hydrogen as a molecular weight regulator are present. Suitable unsaturated hydrocarbon monomers are ethylene, propylene, n-butene-l. n- pentene-1, n-hexene-1, 4-methyl pentene-1 and n-octene-1, used alone or as a mixture. If a separate solvent is used, this may be an inert hydrocarbon having 3 to 8 carbon atoms such as propane, n-butane, isobutane, isobutylene, nhexane, n-heptane or xylene. Furthermore, when the unsaturated hydrocarbon monomer other than ethylene to be polymerized is liquid in the polymerization reactor, this monomer can be also used as the solvent.
The olefin polymerization catalyst may be a catalyst comprising a transition metal compound such as a halogenated titanium compound (e.g., titanium tetrachloride, titanium tetrabromide, titanium trichloride or titanium tribromide), a halogenated vanadium compound (e.g., vanadyl chloride or vanadium tetrachloride) or chromium oxide, and an organometallic compound of Group la, Ia or Illa of the Periodic Table such as an organoaluminum compound (e.g., diethylaluminum chloride or triethylaluminum) or an organomagnesium compound (e.g., diethyl magnesium).
It is not always necessary for the hydrogen, used as a molecular weight regulator, to be present. As the polymerization proceeds, polymerization heat is generated to thereby cause evaporation of the solvent and/or the monomer.
The gas phase portion in the polymerization reactor contains the monomer and hydrogen in addition to the gaseous solvent. A gas mixture is withdrawn from the gas phase portion and introduced as a gas to be condensed through a piping 4 into a washing apparatus-containing reflux condenser 3. At this time, active catalyst particles are entrained in the gas mixture.
When the gas mixture enters the washing apparatus-containing reflux condenser 3, it first comes in countercurrent contact with the condensed liquid which has been condensed on the surface of a heat transfer tube 12 of the condenser, on a washing apparatus (tray) 13. The countercurrent contact washes off the active catalyst particles and polymer particles entrained in the gas mixture.
Then the gas mixture comes in contact with the surface of the heat transfer tube 12 where it is condensed in an amount corresponding to the quantity of heat to be removed in the polymerization reactor. The condensed liquid falls on the washing apparatus 13 where it countercurrently contacts with the gas mixture from the polymerization reaction as described above, and it then returns through piping 8 to the polymerization reactor 1 while containing therein the active catalyst particles and polymer particles.
An uncondensed gas mixture containing the monomer and hydrogen that do not condense on the surface of the heat transfer tube 12 is withdrawn through piping 6 and circulated by a compressor 1 5 into the liquid phase portion of the polymerization reactor 1.
As is well known to one skilled in the art, the heat quantity to be removed is controlled by regulating the condensation amount in the reflux condenser. The amount of the liquid being condensed can be controlled by the amount of cooling water which is supplied through piping 10 into the interior of the heat transfer tube 12 of the condenser. The amount of the cooling water is regulated with a control valve 1 The heat quantity being removed neariy corresponds to the polymerization heat generated by the polymerization in the polymerization reactor 1.
Thus, the heat removal is carried out by controlling the flow amount of the cooling water so that the temperature of the polymerization reactor 1 is maintained at a constant level.
Although the above explanation has been given for a vertical type of multitubular reflux condenser containing therein a washing apparatus, this invention is not limited thereto; constructions as illustrated in Figures 1 and 2 can easily be employed in this invention.
This invention is described in greater detail by reference to the following Example and
Comparative Example.
EXAMPLE
Polymerization was carried out according to the flow diagram shown in Figure 3. The removal of polymerization heat was carried out using an apparatus shown in Figure 4.
Polymerization Reactor: 30 m3 polymerization reactor with a stirrer
Reflux Condenser: vertical type of U-shaped multitubular reflux condenser (heat transfer area: 40 m3)
Washing Apparatus: one-stage turbogrid tray with a down comer which is contained in the lower portion of the reflux condenser
Monomer and Solvent: propylene
Polymerization Catalyst: titanium trichloride and diethylaluminum chloride (feed amount: 1 56 g/hr and 1,000 g/hr, respectively)
Molecular Weight Regulator: hydrogen
Temperature of Polymerization Reactor: 700C
Pressure of Polymerization Reactor: 31 kg/cm2 (Gauge)
The operation was continued for 8 months under the above conditions. Under these conditions, a slurry of polymer produced was discharged from the reactor at an average rate of 2,350 kg/hr.The slurry comprised a solid polymer (produced at an average rate of 1,250 kg/hr), and liquid propylene containing atactic polymer and dissolved catalyst (1,100 kg/hr on average). The quantity of heat removal in the reflux condenser was 400,000 Kcal/hr.
At the end of the time, the reflux condenser was dismantled and inspected. This inspection revealed that almost no deposition of particles of polymer or catalyst on the surface of the heat transfer tube took place. It was observed that the polymer was deposited in a thickness of 6 mm on the walls of the inlet piping through which the gas mixture was introduced into the polymerization reactor.
COMPARATIVE EXAMPLE
The procedure of the Example was repeated with the exception that the washing apparatus (tray 13 and down comer 14) was not provided.
The operation was continued for 33 days. At the end of this time, the reflux condenser was dismantled and inspected; polymer containing catalyst particles were deposited onto the whole surface of the heat transfer tube in a thickness of 0.1 mmto10mm.
Claims (9)
1. A method for removal of heat from a polymerization reactor having a reflux condenser, in which an unsaturated hydrocarbon monomer having 2 to 8 carbon atoms is polymerized in an inert hydrocarbon or in the liquefied monomer having 3 to 8 carbon atoms as a solvent in the presence of an olefin polymerization catalyst, the heat being removed by introducing a gas mixture withdrawn from the polymerization reactor into the reflux condenser where the gas mixture is condensed and separated into a condensed liquid and an uncondensed gas and returning the condensed liquid to the polymerization reactor and the uncondensed gas into the liquid phase in the polymerization reactor by use of a compressor, characterised by washing the gas mixture after it leaves the polymerization reactor and before it reaches the heat transfer surface of the reflux condenser.
2. A method as claimed in Claim 1, wherein the washing of the gas mixture is performed by bringing it in countercurrent contact with the condensed liquid obtained in the reflux condenser and/or the solvent to be supplied to the polymerization reactor.
3. Apparatus for removal of heat from a polymerization reactor with a reflux condenser for use in the method of Claim 1, which apparatus is characterised by including means for washing the gas mixture after it leaves the polymerization reactor and before it reaches the heat transfer surface of the reflux condenser.
4. Apparatus as claimed in Claim 3, wherein the means for washing the gas mixture is so designed that the gas mixture is brought in countercurrent contact with the condensed liquid obtained in the reflux condenser and/or the solvent to be supplied to the polymerization reactor.
5. Apparatus as claimed in Claim 3 or 4, wherein the means for washing the gas mixture is a sieve tray, a turbogrid or a ripple tray.
6. Apparatus as claimed in Claim 3 or 4, wherein the means for washing the gas mixture is a pibo disc scrubber or a cyclone scrubber.
7. Apparatus as claimed in Claim 3 or 4, wherein the means for washing the gas mixture is a spray tower.
8. A method as claimed in Claim 1, substantially as hereinbefore described with reference to the foregoing Example.
9. Apparatus as claimed in Claim 3, substantially as hereinbefore described with reference to the accompanying drawings.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8103699A GB2069369B (en) | 1981-02-06 | 1981-02-06 | Method and apparatus for removal of heat from an olefin polymerization reactor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8103699A GB2069369B (en) | 1981-02-06 | 1981-02-06 | Method and apparatus for removal of heat from an olefin polymerization reactor |
Publications (2)
Publication Number | Publication Date |
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GB2069369A true GB2069369A (en) | 1981-08-26 |
GB2069369B GB2069369B (en) | 1984-04-18 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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GB8103699A Expired GB2069369B (en) | 1981-02-06 | 1981-02-06 | Method and apparatus for removal of heat from an olefin polymerization reactor |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2524896A1 (en) * | 1982-04-07 | 1983-10-14 | Cosden Technology | ISOBUTYLENE POLYMERIZATION PROCESS |
EP0136559A2 (en) * | 1983-09-01 | 1985-04-10 | Kuraray Co., Ltd. | Process for continuous production of ethylene-vinyl acetate copolymer |
FR2590579A1 (en) * | 1985-11-25 | 1987-05-29 | Mitsui Toatsu Chemicals | PROCESS FOR HOMO- OR COPOLYMERIZING PROPYLENE |
US4752640A (en) * | 1984-07-27 | 1988-06-21 | Kanegafuchi Chemical Industry Co., Ltd. | Temperature controlling method for polymerization reactors |
EP0583789A1 (en) * | 1992-08-20 | 1994-02-23 | Daicel Chemical Industries, Ltd. | Method of controlling reactions |
-
1981
- 1981-02-06 GB GB8103699A patent/GB2069369B/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2524896A1 (en) * | 1982-04-07 | 1983-10-14 | Cosden Technology | ISOBUTYLENE POLYMERIZATION PROCESS |
EP0136559A2 (en) * | 1983-09-01 | 1985-04-10 | Kuraray Co., Ltd. | Process for continuous production of ethylene-vinyl acetate copolymer |
EP0136559A3 (en) * | 1983-09-01 | 1985-10-30 | Kuraray Co., Ltd. | Process for continuous production of ethylene-vinyl acetate copolymer |
US4752640A (en) * | 1984-07-27 | 1988-06-21 | Kanegafuchi Chemical Industry Co., Ltd. | Temperature controlling method for polymerization reactors |
FR2590579A1 (en) * | 1985-11-25 | 1987-05-29 | Mitsui Toatsu Chemicals | PROCESS FOR HOMO- OR COPOLYMERIZING PROPYLENE |
EP0583789A1 (en) * | 1992-08-20 | 1994-02-23 | Daicel Chemical Industries, Ltd. | Method of controlling reactions |
Also Published As
Publication number | Publication date |
---|---|
GB2069369B (en) | 1984-04-18 |
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Legal Events
Date | Code | Title | Description |
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PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 20000206 |