CN114682194A - Final polycondensation reaction kettle and application thereof - Google Patents

Final polycondensation reaction kettle and application thereof Download PDF

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Publication number
CN114682194A
CN114682194A CN202011638288.7A CN202011638288A CN114682194A CN 114682194 A CN114682194 A CN 114682194A CN 202011638288 A CN202011638288 A CN 202011638288A CN 114682194 A CN114682194 A CN 114682194A
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final polycondensation
polycondensation reaction
reaction kettle
reaction
feeding
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CN202011638288.7A
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Chinese (zh)
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CN114682194B (en
Inventor
黄娟
高甲
史路飞
吴华志
董志坚
徐洪强
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China Petroleum and Chemical Corp
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China Petroleum and Chemical Corp
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/18Stationary reactors having moving elements inside
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/0006Controlling or regulating processes
    • B01J19/0013Controlling the temperature of the process
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/0053Details of the reactor
    • B01J19/0066Stirrers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/78Preparation processes
    • C08G63/785Preparation processes characterised by the apparatus used

Abstract

The invention discloses a final polycondensation reaction kettle and application thereof, wherein a discharge section of the final polycondensation reaction kettle is in a step shape, an inclination angle from the top to the bottom of the discharge section is 2-30 degrees, a feeding mixing device is further arranged at the bottom of a feeding section of the final polycondensation reaction kettle, and a kettle cavity of the reaction kettle can be controlled in a segmented manner. The reaction materials firstly enter the final polycondensation reaction kettle from the feeding section, then are fully mixed with the additives through the feeding and mixing device, then are subjected to final polycondensation reaction, and finally, the product slowly flows out from the stepped discharging section. The final polycondensation reaction kettle can accurately control the reaction temperature in different reaction stages, and the feeding and mixing device enables the reaction materials and the additives to be mixed more uniformly, so that the reaction uniformity and the reaction efficiency are improved; in addition, the ladder is discharged slowly, both can guarantee the smooth and easy of the ejection of compact, can control ejection of compact speed again to the dwell time of effective control reaction material guarantees the material fully react, has avoided staying too long and has taken place thermal degradation side reaction simultaneously.

Description

Final polycondensation reaction kettle and application thereof
Technical Field
The invention relates to a final polycondensation reaction kettle and application thereof, in particular to a final polycondensation reaction kettle capable of meeting tackifying requirements and application thereof.
Background
When the traditional horizontal polycondensation kettle is used for polycondensation reaction, materials move from the front end to the rear end of the reaction kettle only by virtue of a fluid driving force provided by a material stirring paddle, and the polycondensation reaction is gradually completed. However, when producing polyester with higher viscosity, the material is often accumulated at the front end of the reaction kettle due to the larger viscosity difference of the material before and after the reaction kettle, especially in the polycondensation kettle with large viscosity increasing gradient, so that the material is difficult to flow from the front end to the rear end of the reaction kettle, and the material level at the front end and the rear end is difficult to establish, thereby limiting the viscosity increasing capability of the reaction kettle. Meanwhile, the accumulated materials at the front end can be degraded due to long residence time, so that the quality of the polyester is reduced.
Disclosure of Invention
The invention aims to: the first purpose of the invention is to provide a final polycondensation reaction kettle, and the second purpose is to provide the application of the final polycondensation reaction kettle.
The technical scheme is as follows: the final polycondensation reaction kettle cavity comprises a feeding section and a discharging section, wherein the discharging section is in a step shape and is arranged into 2-30 steps, and the inclination angle from the top to the bottom of the discharging section is 2-30 degrees.
The ejection of compact section sets up certain angle of inclination, can guarantee the smooth and easy ejection of compact of high viscosity result, and the product is through the slow ejection of compact of decurrent ladder, both can guarantee the smooth and easy of the ejection of compact, can control ejection of compact speed again to effective control reaction material's dwell time guarantees that the material fully reacts, has avoided staying too for a long time simultaneously and has taken place thermal degradation side reaction. If the inclination angle is too small, the resistance caused by the viscosity of the material cannot be overcome, and the material still cannot be discharged smoothly and effectively; if the inclination angle is too large or the conventional inclined plane design is adopted, the discharging speed is too high, the materials are discharged before full polycondensation, and the product cannot meet the viscosity requirement.
Further, a feeding and mixing device is arranged at the bottom of the feeding section of the final polycondensation reaction kettle, one side of the feeding and mixing device is communicated with a feeding hole of the final polycondensation reaction kettle, and the rest surfaces of the feeding and mixing device are provided with first through holes; an additive feeding cavity is arranged in the feeding and mixing device, and a second through hole is formed in one side, facing the feeding direction of the reaction materials, of the additive feeding cavity. More closely, the aperture of first through-hole is 5 ~ 20mm, the aperture of second through-hole is 1 ~ 5 mm.
When the final polycondensation reaction kettle operates, the additive enters the cavity of the feeding and mixing device through the second through hole in the additive feeding cavity, then is fully mixed with the reaction material entering through the feeding hole of the final polycondensation reaction kettle in the cavity of the feeding and mixing device, and finally the mixed material enters the cavity of the final polycondensation reaction kettle through the first through hole to carry out final polycondensation reaction. Compared with the existing mixing mode of directly throwing in, the reaction materials are high in viscosity and cannot be directly mixed uniformly, so that the reaction rates of the reaction materials at different sites are different, and the quickly generated product stays in the kettle cavity for too long time, so that the thermal degradation reaction is easier to occur. In addition, this feed mixing device can realize continuous feeding and mixing, improves production efficiency to can effectively guarantee continuous mixing's homogeneity.
The aperture of the second through hole is set, so that the additive can be dispersed into a uniform material flow with proper size and can smoothly enter the cavity of the feeding and mixing device, and meanwhile, the viscosity of the reaction material is higher than that of the additive, so that the reaction material cannot enter the additive cavity to block the cavity; first through-hole aperture sets up slightly greatly, can guarantee that the mixture of higher viscosity smoothly gets into the polycondensation reation kettle cauldron intracavity, can effectively guarantee the material simultaneously at feeding mixing arrangement's dwell time, effectively guarantee the mixing time and mix the degree of consistency.
Furthermore, the outside of the final polycondensation reaction kettle cavity is provided with a sectional type heating cavity which is specifically divided into a front section heating cavity and a rear section heating cavity.
Because the reaction materials are polycondensed and tackified in the final polycondensation reaction kettle, the reaction conditions required by different reaction stages are different, and the traditional integrated heating cavity can only control a single reaction temperature and cannot accurately control the temperature of the materials in different reaction processes. The sectional type heating cavity can control the temperature respectively according to the material reaction process, and different heating media can be selected according to the material characteristics.
Further, the bottom of the front part of the kettle cavity of the final polycondensation reaction kettle is provided with a heating partition plate, non-heating partition plates can be alternately arranged with the heating partition plate, and the preferred arrangement mode is that 2-4 heating partition plates and 1-3 non-heating partition plates are alternately arranged.
Because the reaction material has lower viscosity and good fluidity at the front section of the final polycondensation reaction kettle, the heating baffle plate is arranged at the bottom of the final polycondensation reaction kettle, so that the heating effect of the material at the bottom of the front section can be enhanced, meanwhile, the retention time of the material at the low-viscosity section is ensured, and the tackifying effect is improved. The non-heating partition plates are arranged at intervals, so that the materials can be prevented from being continuously in a continuous high-temperature state, and thermal degradation side reaction generated by transitional heating is avoided.
Further, the final polycondensation reaction kettle is a bedroom double-stirring-shaft reaction kettle, a dumbbell-shaped stirring blade is arranged on the stirring shaft, and a scraper is further arranged at the end part of the dumbbell-shaped stirring blade.
The blade surface of the dumbbell-shaped stirring blade is of a hollow structure, a scraper at the end part of the dumbbell-shaped stirring blade is vertical to the blade surface, so that the reaction material can be effectively filmed and tackified, and the blade and the scraper are in tangential fit with the inner wall of a kettle cavity of the final polycondensation reaction kettle, so that the material accumulation on the kettle cavity can be effectively prevented; simultaneously, two (mixing) shaft rotation direction are opposite, and the scraper blade on one of them (mixing) shaft is further tangent laminating with another (mixing) shaft and the paddle on it, can also effectively prevent that the material on (mixing) shaft and the paddle from piling up, has multiple clean effect. In addition, the specific shape of the blade surface and the scraper plate also play a role in baffle and material diversion, so that the reaction materials are pushed forward in the kettle cavity, and even the reaction at low liquid level can be carried out smoothly.
The final polycondensation reaction kettle can be applied to polyester preparation, wherein the polyester is not limited to polybutylene terephthalate (PBT), polyethylene terephthalate (PET), polytrimethylene terephthalate (PTT), poly (butylene terephthalate-co-butylene adipate) ester (PBAT), poly (butylene terephthalate-co-butylene succinate) ester (PBST), polybutylene succinate adipate (PBSA), polybutylene succinate (PBS) and thermoplastic polyester elastomer (TPEE).
Has the advantages that: compared with the prior art, the invention has the following remarkable advantages:
(1) the residence time of the materials can be accurately controlled, the polycondensation reaction degree of the reaction materials is effectively improved, the viscosity of the product is improved, and meanwhile, the high-viscosity product can be smoothly discharged;
(2) the full and uniform mixing of the reaction materials and the additives can be effectively ensured, the uniformity of the reaction is improved, the occurrence of side reactions is reduced, the continuous operation can be realized, and the process efficiency is improved;
(3) the reaction temperature can be accurately controlled to meet the requirements of the processes in different reaction process stages;
(4) the reaction kettle has wide application range and can meet the requirements of different products and process batches.
Drawings
FIG. 1 is a schematic view of a finishing reactor according to the present invention;
FIG. 2 is a sectional view of the discharge section of the final polycondensation reaction vessel in accordance with the present invention;
FIG. 3 is a cross-sectional view of a feed mixing device of a final polycondensation reaction vessel in accordance with the present invention;
FIG. 4 is a sectional view of a final polycondensation reaction vessel according to the present invention.
Detailed Description
The technical scheme of the invention is further explained by combining the attached drawings.
Implementation 1: final polycondensation reaction kettle
As shown in figures 1 and 2, a final polycondensation reaction kettle cavity 1 comprises a feeding section and a discharging section, wherein the discharging section is in a step shape and is provided with 2-30 steps, and the inclination angle from the top to the bottom of the discharging section is 2-30 degrees. The end of the discharging section is connected with a discharging port 5.
The ejection of compact section sets up to certain angle of inclination, can guarantee the smooth and easy ejection of compact of high viscosity result, and the product is through the slow ejection of compact of decurrent ladder, both can guarantee the smooth and easy of the ejection of compact, can control ejection of compact speed again to effective control reaction material's dwell time guarantees that the material fully reacts, has avoided staying too for a long time simultaneously and has taken place thermal degradation side reaction. If the inclination angle is too small, the resistance caused by the viscosity of the material cannot be overcome, and the material still cannot be discharged smoothly and effectively; if the inclination angle is too large or the conventional inclined plane is adopted, the discharging speed is too high, the materials are discharged before full polycondensation, and the product cannot meet the viscosity requirement.
As shown in fig. 1 and fig. 3, a feed mixing device 20 is arranged at the bottom of the feed section of the final polycondensation reaction kettle, one side of the feed mixing device 20 is communicated with the feed inlet 3 of the final polycondensation reaction kettle, and the rest surfaces are provided with first through holes 202; an additive feeding cavity 201 is arranged in the feeding and mixing device 20, an additive feeding port 4 is arranged at the lower part of the additive feeding cavity 201, and a second through hole 203 is arranged at one side of the additive feeding cavity 201 facing the feeding direction of the reaction materials. The aperture of the first through hole 202 is 5-20 mm, and the aperture of the second through hole 203 is 1-5 mm.
When the final polycondensation reaction kettle operates, the additive enters the additive feeding cavity 201 from the additive feeding port 4, then enters the cavity of the feeding and mixing device 20 through the second through hole 203, and then is fully mixed with the reaction material entering through the feeding port 3 of the final polycondensation reaction kettle in the cavity of the feeding and mixing device 20, and finally the mixed material enters the final polycondensation reaction kettle cavity 1 through the first through hole 202 to perform final polycondensation reaction. Compared with the existing mixing mode of directly throwing in, the reaction materials are high in viscosity and cannot be directly mixed uniformly, so that the reaction rates of the reaction materials at different sites are different, and the quickly generated product stays in the kettle cavity for too long time, so that the thermal degradation reaction is easier to occur. In addition, this feeding mixing arrangement 20 can realize continuous feeding and mix, improves production efficiency to can effectively guarantee the homogeneity of continuous mixing.
The aperture of the second through hole 203 is set to ensure that the additive is dispersed into a uniform material flow with a proper size and smoothly enters the cavity of the feeding and mixing device 20, and meanwhile, the viscosity of the reaction material is higher than that of the additive, so that the reaction material does not enter the additive feeding cavity 201 to block the cavity; the aperture of the first through hole 202 is slightly larger, so that the mixed material with higher viscosity can smoothly enter the final polycondensation reaction kettle cavity 1, and meanwhile, the residence time of the material in the feeding and mixing device 20 can be effectively ensured, and the mixing time and the mixing uniformity are effectively ensured.
As shown in fig. 1, a sectional heating cavity 2 is arranged outside a final polycondensation reaction kettle cavity 1, and is specifically divided into a front-stage heating cavity and a rear-stage heating cavity. The front-stage heating cavity heat medium inlet 15 and the rear-stage heating cavity heat medium inlet 17 are arranged at the bottom of the kettle cavity 1, and the front-stage heating cavity heat medium outlet 16 and the rear-stage heating cavity heat medium outlet 18 are arranged at the top of the kettle cavity 1.
Because the reaction materials are polycondensed and tackified in the final polycondensation reaction kettle, the reaction conditions required by different reaction stages are different, and the traditional integrated heating cavity can only control single reaction temperature and cannot accurately control the temperature of the materials in different reaction processes. The sectional heating cavity 2 can control the temperature respectively according to the material reaction process, and different heating media can be selected according to the material characteristics.
As shown in fig. 1, the bottom of the front portion of the final polycondensation reaction kettle cavity 1 is provided with heating partition plates 11, and may also be provided with non-heating partition plates 12 alternately, and the preferred arrangement mode is that 4 heating partition plates 11 and 3 non-heating partition plates 12 are alternately arranged. The heating separator heat medium inlet 13 is arranged at the bottom of the kettle cavity 1, and the heating separator heat medium outlet 14 is arranged at the top of the kettle cavity 1.
As the reaction material has lower viscosity and good fluidity at the front section of the final polycondensation reaction kettle, the heating baffle 11 arranged at the bottom of the final polycondensation reaction kettle can enhance the heating effect of the material at the bottom of the front section, ensure the retention time of the material at the low-viscosity section and improve the tackifying effect. The non-heating partition plates 12 are arranged at intervals, so that the materials can be prevented from being continuously in a continuous high-temperature state, and thermal degradation side reaction caused by transitional heating is avoided.
As shown in fig. 4, the final polycondensation reaction kettle is a bedroom double-stirring-shaft reaction kettle, a dumbbell-shaped stirring blade 21 is arranged on the stirring shaft, and a scraper 211 is further arranged at the end of the dumbbell-shaped stirring blade 21. The first stirring shaft 7 and the second stirring shaft 8 penetrate through the kettle cavity 1 in parallel, and the rotating speed is controlled by a motor 10 and a reduction gearbox 9 and ranges from 2 rpm to 10 rpm. The double stirring shafts drive the dumbbell-shaped stirring blades 21 and the scraper 211 to rotate, and 24 pairs of dumbbell-shaped stirring blades 21 are arranged in parallel on the first stirring shaft 7 and the second stirring shaft 8.
The dumbbell-shaped stirring blades 21 are hollow in blade surface, the scrapers 211 at the end parts of the dumbbell-shaped stirring blades are vertical to the blade surface, so that the reaction materials can be effectively filmed and tackified, and the dumbbell-shaped stirring blades 21 and the scrapers 211 are in tangent fit with the inner wall of the reaction kettle cavity 1, so that the materials on the kettle cavity 1 can be effectively prevented from being accumulated; simultaneously, first (mixing) shaft 7 and 8 opposite direction of rotation of second (mixing) shaft, scraper blade 211 on one of them (mixing) shaft is further tangent laminating with another (mixing) shaft and dumbbell shape stirring paddle 21 on it, can also effectively prevent that the material on (mixing) shaft and the paddle from piling up to be equipped with cleaning medium entry 19 at cauldron chamber 1 top, the cooperation is sprayed the washing, can carry out periodic cleaning maintenance to cauldron chamber 1, has multiple clean function. In addition, the specific shape of the blade surface and the scraper 211 also play the roles of a baffle and material diversion, so that the reaction materials are pushed forwards in the kettle cavity 1, and even the low-liquid-level reaction can be carried out smoothly.
In addition, the dumbbell-shaped stirring blades 21 can drive a vapor phase byproduct generated in the polycondensation reaction to volatilize to the upper part of the kettle cavity 1 by matching with the scraper 211, the vapor phase byproduct is discharged through a vapor phase outlet 6 arranged at the top of the kettle cavity 1, and the vapor phase byproduct enters a post-treatment step.
The final polycondensation reaction kettle can be applied to polyester preparation, wherein the polyester is not limited to polybutylene terephthalate (PBT), polyethylene terephthalate (PET), polytrimethylene terephthalate (PPT), poly (butylene terephthalate-co-butylene adipate) ester (PBAT), poly (butylene terephthalate-co-butylene succinate) ester (PBST), polybutylene succinate adipate (PBSA), polybutylene succinate (PBS) and thermoplastic polyester elastomer (TPEE). The final polycondensation reaction kettle has excellent tackifying capability, and can be used for polycondensing a prepolymer with the intrinsic viscosity of 0.2-0.7 dL/g to a PBAT final condensate with the intrinsic viscosity of 0.7-1.6 dL/g.

Claims (10)

1. The final polycondensation reaction kettle is characterized in that a kettle cavity (1) of the final polycondensation reaction kettle comprises a feeding section and a discharging section, wherein the discharging section is in a step shape and is arranged into 2-30 steps, and the inclination angle from the top to the bottom of the discharging section is 2-30 degrees.
2. The final polycondensation reaction kettle according to claim 1, wherein a feed mixing device (20) is arranged at the bottom of the feed section of the final polycondensation reaction kettle, one side of the feed mixing device (20) is communicated with the feed inlet (3) of the final polycondensation reaction kettle, and the rest surface is provided with a first through hole (202); an additive feeding cavity (201) is arranged in the feeding and mixing device 20, and a second through hole (203) is formed in one side, facing the feeding direction of the reaction materials, of the additive feeding cavity (201).
3. The final polycondensation reaction vessel according to claim 2, wherein the first through-hole (202) has a pore diameter of 5 to 20mm, and the second through-hole (203) has a pore diameter of 1 to 5 mm.
4. The final polycondensation reaction vessel of claim 1 wherein the final polycondensation reaction vessel 1 is externally provided with a segmented heating chamber (2).
5. The final polycondensation reactor of claim 4 wherein the staged heating chamber (2) is divided into a front stage heating chamber and a rear stage heating chamber.
6. The final polycondensation reaction kettle according to claim 1, wherein a heating partition (11) is provided at the bottom of the front portion of the final polycondensation reaction kettle cavity (1).
7. The final polycondensation reaction kettle according to claim 6, wherein a non-heating partition (12) is further arranged at the bottom of the front part of the final polycondensation reaction kettle cavity (1), and the heating partitions (11) and the non-heating partitions (12) are alternately arranged.
8. The final polycondensation reaction kettle according to claim 1, wherein the final polycondensation reaction kettle is a bedroom double stirring shaft reaction kettle, and a dumbbell-shaped stirring blade (21) is arranged on the stirring shaft.
9. The final polycondensation reaction vessel according to claim 8, wherein the ends of the dumbbell-shaped stirring blades (21) are provided with scrapers (211).
10. Use of a finishing reactor according to any one of claims 1 to 9 for the preparation of polyesters.
CN202011638288.7A 2020-12-31 2020-12-31 Final polycondensation reaction kettle and application thereof Active CN114682194B (en)

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CN114682194B CN114682194B (en) 2024-01-26

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Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10146524A (en) * 1996-09-18 1998-06-02 Toyo Denki Kogyosho:Kk Method and apparatus for producing stable solution
JPH11124493A (en) * 1997-10-23 1999-05-11 Teijin Ltd Production of modified polyester
JPH11302388A (en) * 1998-04-21 1999-11-02 Konica Corp Preparation of cellulose acylate solution, production of cellulose acylate film and cellulose acylate film
CN101245143A (en) * 2008-03-21 2008-08-20 哈尔滨工业大学 Continuous polymerization reaction device for producing poly-p-phenylene benzo dioxazole
JP2011116915A (en) * 2009-12-07 2011-06-16 Hitachi Plant Technologies Ltd Polymerizer of polyester
CN203316118U (en) * 2013-03-22 2013-12-04 中国昆仑工程公司 Y-shaped rotor polymerization reactor
CN106281724A (en) * 2016-08-29 2017-01-04 繁昌县健文电子商务有限公司 A kind of material multi mixed reactor
CN206454310U (en) * 2017-02-13 2017-09-01 安徽翠鸟生物技术有限公司 A kind of premixed stirring extraction device
JP2018150453A (en) * 2017-03-13 2018-09-27 三菱ケミカル株式会社 Manufacturing method of polybutylene succinate
CN111468062A (en) * 2020-06-01 2020-07-31 扬州普立特科技发展有限公司 Horizontal stirring reactor with heat exchange partition plate
CN111841449A (en) * 2020-08-18 2020-10-30 北京拓川科研设备股份有限公司 Method of experimental equipment for discharging polyethylene slurry
CN211800630U (en) * 2020-03-23 2020-10-30 江阴市博生新材料科技有限公司 A circulation feeding device for polyarylate production

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10146524A (en) * 1996-09-18 1998-06-02 Toyo Denki Kogyosho:Kk Method and apparatus for producing stable solution
JPH11124493A (en) * 1997-10-23 1999-05-11 Teijin Ltd Production of modified polyester
JPH11302388A (en) * 1998-04-21 1999-11-02 Konica Corp Preparation of cellulose acylate solution, production of cellulose acylate film and cellulose acylate film
CN101245143A (en) * 2008-03-21 2008-08-20 哈尔滨工业大学 Continuous polymerization reaction device for producing poly-p-phenylene benzo dioxazole
JP2011116915A (en) * 2009-12-07 2011-06-16 Hitachi Plant Technologies Ltd Polymerizer of polyester
CN203316118U (en) * 2013-03-22 2013-12-04 中国昆仑工程公司 Y-shaped rotor polymerization reactor
CN106281724A (en) * 2016-08-29 2017-01-04 繁昌县健文电子商务有限公司 A kind of material multi mixed reactor
CN206454310U (en) * 2017-02-13 2017-09-01 安徽翠鸟生物技术有限公司 A kind of premixed stirring extraction device
JP2018150453A (en) * 2017-03-13 2018-09-27 三菱ケミカル株式会社 Manufacturing method of polybutylene succinate
CN211800630U (en) * 2020-03-23 2020-10-30 江阴市博生新材料科技有限公司 A circulation feeding device for polyarylate production
CN111468062A (en) * 2020-06-01 2020-07-31 扬州普立特科技发展有限公司 Horizontal stirring reactor with heat exchange partition plate
CN111841449A (en) * 2020-08-18 2020-10-30 北京拓川科研设备股份有限公司 Method of experimental equipment for discharging polyethylene slurry

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