GB2082597A - A method of continuous polymerization - Google Patents

A method of continuous polymerization Download PDF

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Publication number
GB2082597A
GB2082597A GB8116942A GB8116942A GB2082597A GB 2082597 A GB2082597 A GB 2082597A GB 8116942 A GB8116942 A GB 8116942A GB 8116942 A GB8116942 A GB 8116942A GB 2082597 A GB2082597 A GB 2082597A
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United Kingdom
Prior art keywords
paddles
polymerization
shafts
reactor
action
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Granted
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GB8116942A
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GB2082597B (en
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Polyplastics Co Ltd
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Polyplastics Co Ltd
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Publication of GB2082597A publication Critical patent/GB2082597A/en
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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B7/00Mixing; Kneading
    • B29B7/30Mixing; Kneading continuous, with mechanical mixing or kneading devices
    • B29B7/34Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices
    • B29B7/38Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices rotary
    • B29B7/46Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices rotary with more than one shaft
    • B29B7/48Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices rotary with more than one shaft with intermeshing devices, e.g. screws
    • B29B7/482Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices rotary with more than one shaft with intermeshing devices, e.g. screws provided with screw parts in addition to other mixing parts, e.g. paddles, gears, discs
    • B29B7/483Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices rotary with more than one shaft with intermeshing devices, e.g. screws provided with screw parts in addition to other mixing parts, e.g. paddles, gears, discs the other mixing parts being discs perpendicular to the screw axis
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01FMIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
    • B01F27/00Mixers with rotary stirring devices in fixed receptacles; Kneaders
    • B01F27/60Mixers with rotary stirring devices in fixed receptacles; Kneaders with stirrers rotating about a horizontal or inclined axis
    • B01F27/73Mixers with rotary stirring devices in fixed receptacles; Kneaders with stirrers rotating about a horizontal or inclined axis with rotary discs
    • B01F27/731Mixers with rotary stirring devices in fixed receptacles; Kneaders with stirrers rotating about a horizontal or inclined axis with rotary discs with two or more parallel shafts provided with perpendicularly mounted discs, e.g. lens shaped, one against the other on each shaft and in circumferential contact with the discs on the other shafts, e.g. for cleaning
    • 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
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/36Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die
    • B29C48/395Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders
    • B29C48/40Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders using two or more parallel screws or at least two parallel non-intermeshing screws, e.g. twin screw extruders
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/36Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die
    • B29C48/395Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders
    • B29C48/40Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders using two or more parallel screws or at least two parallel non-intermeshing screws, e.g. twin screw extruders
    • B29C48/405Intermeshing co-rotating screws
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/36Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die
    • B29C48/395Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders
    • B29C48/40Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders using two or more parallel screws or at least two parallel non-intermeshing screws, e.g. twin screw extruders
    • B29C48/41Intermeshing counter-rotating screws
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00Processes of polymerisation
    • C08F2/02Polymerisation in bulk
    • 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
    • C08G2/00Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
    • C08G2/10Polymerisation of cyclic oligomers of formaldehyde

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
  • Polymerisation Methods In General (AREA)
  • Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)

Abstract

A method of continuous polymerization of a liquid polymerization medium to obtain fine particles of polymer product is disclosed, the reaction being continuously effected in a polymerization reactor wherein mixing is effected by the action of a plurality of paddles mounted on each of dual rotating shafts (3,4), characterised in that the said dual shafts rotate in reverse directions to each other, and the said paddles are enclosed by walls of the said reactor the inside surface (9) of the said walls closely defining the surface generated by the rotation of the ends of both sets of paddles; the ends of major axes of the said paddles on one rotating shaft periodically approaching the ends of minor axes of the corresponding paddles on the other rotating shaft to effect a mixing action as well as a longitudinal shearing action across a notional interface between said two shafts. The method is particularly useful for the polymerization of trioxan. <IMAGE>

Description

SPECIFICATION A method of continuous polymerization This invention relates to a method of continuous polymerization of a liquid polymerization medium to obtain fine particles of polymer product, the reaction being continuously effected in a polymerization reactor wherein mixing is effected by the action of a plurality of paddles mounted on each of dual rotating shafts.
The homo- or co-polymerization of molten trioxan is widely practised. Thus the production of polyoxymethylene (co-) polymer, is industrially very important in the production of polyacetal resin.
The present invention is particularly suitable to such continuous polymerization of trioxan, although it can be used for other processes wherein a phase change takes place and in which a desired granulating step is required.
When molten trioxan (if desired containing material comonomerfor example one or more of the monomers ethylene oxide, dioxolan, butanediol, formal and diethylene glycol formal) is polymerized in the presence of a strong acid, e.g. phosphorous pentafluoride or perchloric acid or tin chloride or boron trifluoride, to give for example polyoxymethylene, the very rapid reaction rate changes the liquid phase of the polymerization medium into a solid phase through a short intermediate slurry phase.
If the reaction is effected without a comminuting step large blocks of stiff product will be obtained resulting in difficult handling, a deterioration in quality due to accumulated polymerization heat, and lowered polymerization yield. Reaction under a high shearing action is a particularly preferred technique for the prevention of large blocks of product and for providing effective removal of polymerization heat of which various detailed methods have been proposed. A reactor which is a mixer extruder having dual shafts supporting paddles is a useful apparatus because it imparts a high shearing action to the contents. For example published Japanese Patent specification No. 84890/76 discloses a dual shaft mixer comprising a combination of elliptical paddles.Such features have a disadvantage however when used for polymerization reactions in that the dual shafts all rotate in the same direction. The features of this system are the strong shearing action on the contents, a self-cleaning action, the ability to fully granulate the contents of a polymerizing apparatus, and paddles free from polymer adhering thereto. However such advantages are offset by the higher loads that are applied to the rotating shafts, and for safe operation the contents of the vessel must be restricted. For the solution of this problem published Japanese Patent specification No. 86794/78 discloses a method which restricts the degree of high shearing action to a lower value and provides a second reactor of lower shearing action.Such two-stage reaction techniques however restrict the conversion obtained to a specified range, and if it increases too much the load on the final vessel providing high shearing becomes too high, and if the conversion is too low the degree of filling of the second reactor increases so as to cause agglomeration of solid particles leading to a deterioration of quality. Thus the method according to the said Japanese Patent specification No. 8794/78 is limited in adaptability to change of maerial quality and product grade. It is therefore desirable to provide an optimum shearing action in the same reactor in accordance with the progress of reaction.
While it is possible in dual shaft apparatuses using shafts rotating in the same direction to vary the shearing force by changing the pitch of the screws or by changing the clearance inside the apparatus, since the progress of the reaction depends upon slight changes of the reaction conditions and material quality, such apparatus is not readily adaptable.
Thus there is a need for apparatus in which shearing action changes according to the progress of reaction.
Hitherto a paddle-type dual shaft mixer the shafts of which rotate in reverse direction to each other has not been considered as a polymerization apparatus because it effects only low shearing force and it not self-cleaning. However it has now been found that in such a mixer the shearing force automaticaliy changes in the desirable direction corresponding to changes in phase ocurring in liquid phase polymerization reactions.
The invention provides a method of continuous polymerization of a liquid polymerization medium to obtain fine particles of polymer product, the reaction being continuously effected in a polymerization reactor wherein mixing is effected by the action of a plurality of paddles mounted on each of dual rotating shafts, characterised in that the said dual shafts rotate in reverse directions to each other, and the said paddles are enclosed by walls of the said reactor the inside surface of the said walls closely defining the surface generated by the rotation of the ends of both sets of paddles; the ends of major axes of the said paddles on one rotating shaft periodically approaching the ends of minor axes of the corresponding paddles on the other rotating shaft to effect a mixing action as well as a longitudinal shearing action across a notional interface between said two shafts.
The method according to this invention can expeditiously be used for polymerization reactions in which a liquid-to-solid phase-change occurs, particularly for the continuous polymerization of trioxan.
This invention is hereinafter described and illustrated in the accompanying drawings, of which Figure lisa schematic elevation of the mixer reactor 1 used in the method of the invention, the broken portion showing the position of the shafts; Figure 2 is a cross-sectional view on line A-A in Figure 1; and Figure 3 is a partial elevation of a shaft of the mixer.
The mixer 1 includes a closed long narrow space 2 having a cross-section as shown in Figure 2. The space 2 accommodates two shafts 3 and 4. On the first shaft 3 and second shaft 4 are mounted a plurality of paddles 5,6,7,8,... in an arrangement whereby corresponding paddles on both the shafts engage with each other alternately. Successive paddles on the same shaft are displaced for example by 90 or 60 , to vary the mixing characteristics.
Skewed feed paddles 7,8 are also included in the paddles. Around the periphery of the paddles an enclosing wall 9 is provided with its inside surfaces in close contact with the paddles. The mixer 1 has an inlet port for charging the liquid polymerization medium and an outlet port 11 for discharging the solid product. The liquid medium e.g. trioxan is charged from the charging port 10 into one end of the mixer reactor 1, and the catalyst is introduced through the catalyst inlet 12 and mixed with the liquid medium, and the solid product is discharged from the discharging port 11 provided at the other end. The position of the catalyst inlet 12 is not limited to the upper portion of the mixer, and the catalyst can be introduced from any direction. The catalyst can be charged also together with the starting material e.g. trioxan.As shown in Figure 3 a feed screw 13 is positioned near the charging port and pushes forward the contents. The skewed feed paddles 7 arranged between the adjacent nonskewed paddles help to push the contents forward.
The relationship of the movements of paddles and contents when the dual shafts rotate in the same direction or in reverse directions is shown in Figure 4 and Figure 5. Figure 4 shows the movement of the contents when the shafts rotate in the same direction, and Figure 5, when the shafts rotate in reverse directions, the contents shown in hatched outline. In Figure 4 the paddles rotate by 90 in the stages (a) (b) , (c). With respect to the space (B) enclosed by the paddles 5', 6' and walls 9, the space volume, while undergoing some change, is merely moved from right to ieft. Thus, only a small mixing effect is obtained in this process, while the large resistance increases the load applied on the apparatus.In contrast to this in Figure 5, which illustrates the invention, the space (E) in the stage (a) is decreased by compression when moving from stage (b) to (c), the space (G) being gradually expanded. Therefore the contents move in the arrowed direction (F) through the clearance between the paddles 5 and 6, and longitudinal mixing and adequate shearing are effected. There is thus a significant difference between polymerization processes using co-directional rotation of the shafts and by the reverse-directional rotation, as hereafter further described.
As set forth in published Japanese Patent specification No. 86794/78, the polymerization of trioxan is divided into three stages: In the first stage rapid reaction has not yet occurred or the reaction is less than 20% completed, the contents still being in liquid state. The requirements for the reactor mixer in this stage is merely a good mixing ability. In the second stage, reaction proceeds with a rapid phase change from liquid to solid.
The reaction proceeds in the range from 20 to 60% completion. The required properties of the reactor mixer are strong shearing effects and good removal of heat. The third stage results in the formation of fine particles of solid (providing full shearing force has been applied in the preceding stage), the liquid not remaining as a continuous phase. Requirements for the reactor in this stage are slow agitation which is enough to prevent adhesion between solid particles, heat removal, and a retention time to allow for completion of the polymerization. Shearing effects are not required.
A feature of the dual shaft reactor described in the said Japanese Patent specification No. 84890/76 withelliptical paddles rotating in the same direction, which had been considered best before the advant of the present invention, is such that two corresponding paddles rotate always in contact with each other (with self-cleaning effect) and rotate the space defined by the paddles and the walls of the mixer, while changing its volume and shape to effect substantial deformation of the contents. This feature has favourable effect in the first stage of reaction, but the effect arising from the fact that the paddles are always in contact with each other, is small because of the low viscosity of the contents at this stage.These features are favourable also in the second stage where a strong shearing force is required; a reason why the same directional rotation system has been considered desirable. In the third stage, the contents are in substantially the form of solid particles, the volume of which and the interstitial spaces are difficult to change. If such contents are forced to change volume and form, they show a strong resistance and impose a very high load, and therefore the apparatus should be operated at a lower degree of filling. However a low filling degree leads to sinking of solid particles and uneven force exerted on the shafts resulting in bent shafts and increased load. Thus the operative range is extremely limited. To increase the retention time, in addition, the length/diameter ratio must be increased, which will further increase shipping of the rotating shafts.
In contrast, in the dual shaft reactor with paddles rotating in reverse directions used according to this invention, though coupled elliptical paddles content at the end of the major axis of a paddle with the end of the minor axis of the other paddle, other parts of the paddles do not contact each other on rotation.
Thus the reactor is not self-cleaning in the usual sense. In the first stage of reaction, the problem of mixing low viscosity liquids has little correspondence with the direction of rotation, and the apparatus of this invention has a similar function to the same direction rotation apparatus.
In the second stage of reaction high shearing force is required, and the reverse directional rotation apparatus, which is not a self-cleaning type, at first sight appears to be disadvantageous with weak shearing force. In fact however the contents at this stage, having a strong tendency to stick to each other, hardly move from the clearance between the paddles, and good shearing action is effected by the reverse directional rotation apparatus, like the same directional rotation apparatus. The clearance between paddles has little significance. In the third stage wherein solid particles have relatively weak adhesion, the clearance between paddles is of significance in that it allows the particles to move into another space through it. Therefore the resistance and load are kept lower even at higher filling degrees.In addition, since the paddle surface is always rubbed by solid particles, undesirable sticking of polymer hardly occurs in spite of the paddles not being self-cleaning. Thus the reverse directional rotation apparatus has such characteristics that the exertion of the shearing force, that is the load on the apparatus, automatically changes in a desirable direction as the reaction stage proceeds, namely according to the phase change of the contents.
For the above reasons, the same directional rotation reactor and reverse directional rotation reactor cannot be operated under the same conditions. In the conditions that attain enough filling and keep sufficient retention time for the reverse directional rotation reactor, the same directional rotation reactor cannot operate because of greatly raised resistance of the solid filling and the maximum filling degree in the operative range for the same directional rotation reactor is half that for the reverse directional reactor. Even in this range however the shafts of the same directional rotation reactor can be bent during agitation. Because of this whipping effect the clearance between the paddles and the barrel must be made large enough to prevent their contact. This results in a thick layer on the barrel walls leading to poor heat removal and lowered product quality.The operation a lower filling degree extends retention time and also causes lowered quality.
In the reverse directional rotation apparatus used in the method of this invention, the automatic change of characteristics in the same reactor fully responds to the change of reaction rate due to the change of reaction conditions, material quality and grade. Thus the reator used according to this invention permits reaction at a rate from zero to nearly 100% and can be used also as the primary or secondary reactor in a two-stage reaction method.
This invention will be further described with reference to the examples.
Example 1 One hundred parts by weight of trioxan, 2.5 parts by weight of ethylene oxide, and 100 ppm boron trifluoride were charged into a reactor shown in Figure 1. Water at 25"C was passed through the jacket. The shafts were rotated in reverse directions at 45 rpm. After a residence time of about 8 min. a finely powered product was obtained from the discharge port. Unreacted monomer content in the product was about 2%.
Example 2 Materials of the same composition as Example 1 were reacted in the apparatus shown in Figure 1, with a residence time of 2 min. The conversion at the discharge port was 60%. This reactant was further fed into an agitator having paddles inside a cylinder which was water-cooled and agitated for 10 min. The unreacted monomer content in the product taken out of the agitator was 2%.
Comparative experiment Similar polymerization was tried in the same reactor as in Example 1, with the shafts rotated in the same direction. Upon the start of polymerization, the load on the apparatus increased substantially and the shafts whipped so much that the paddles contacted the barrel and stopped the motor. Thus the experiment could not be continued.

Claims (3)

1. A method of continuous polymerization of a liquid polymerization medium to obtain fine particles of polymer product, the reaction being continuously effected in a polymerization reactor wherein mixing is effected by the action of a plurality of paddles mounted on each of dual rotating shafts, characterised in that the said dual shafts rotate in reverse directions to each other, and the said paddles are enclosed by walls of the said reactor the inside surface of the said walls closely defining the surface generated by the rotation of the ends of both sets of paddles; the ends of major axes of the said paddles on one rotating shaft periodically approaching the ends of minor axes of the corresponding paddles on the other rotating shaft to effect a mixing action as well as a longitudinal shearing action across a notional interface between said two shafts.
2. A method according to Claim 1 for the continuous polymerization of trioxan, optionally with a co-monomer.
3. A method according to Claim 1 or Claim 2, substantially as hereinbefore described and illustrated in the accompanying drawings.
GB8116942A 1980-08-22 1981-06-03 A method of continuous polymerization Expired GB2082597B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP55115423A JPS5740520A (en) 1980-08-22 1980-08-22 Continuous polymerization

Publications (2)

Publication Number Publication Date
GB2082597A true GB2082597A (en) 1982-03-10
GB2082597B GB2082597B (en) 1983-11-02

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GB8116942A Expired GB2082597B (en) 1980-08-22 1981-06-03 A method of continuous polymerization

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JP (1) JPS5740520A (en)
KR (1) KR840001754B1 (en)
AU (1) AU547770B2 (en)
BE (1) BE890030A (en)
BR (1) BR8105183A (en)
CA (1) CA1184342A (en)
DE (1) DE3132453A1 (en)
FR (1) FR2488896B1 (en)
GB (1) GB2082597B (en)
HK (1) HK85784A (en)
NL (1) NL188290C (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2537979A1 (en) * 1982-12-21 1984-06-22 Ube Industries PROCESS FOR THE PREPARATION OF FORMALDEHYDE COPOLYMERS
EP0198719A2 (en) * 1985-04-17 1986-10-22 Polyplastics Co. Ltd. Method of continuous polymerization and apparatus therefor
FR2647693A1 (en) * 1989-06-02 1990-12-07 Japan Storage Batterie Cy Ltd Device for preparing a paste of active material for a storage battery (accumulator)

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE813154C (en) * 1949-09-29 1951-09-06 Bayer Ag Mixing and kneading device
DE2020935A1 (en) * 1970-04-29 1971-11-18 Bayer Ag Process for the continuous production of stereospecific elastomers from 1,3-dienes
DE2321854A1 (en) * 1973-04-30 1974-11-14 Werner & Pfleiderer KNEADING AND MIXING MACHINE
DE2362791C2 (en) * 1973-12-18 1982-07-01 Hoechst Ag, 6000 Frankfurt Process for the preparation of copolymers of trioxane
JPS518489A (en) * 1974-07-10 1976-01-23 Hitachi Electronics SETSUTEICHI SEIGYOHOSHIKI
US4105637A (en) * 1974-10-11 1978-08-08 Celanese Corporation Process for producing a polyacetal polymer
DE2550969C2 (en) * 1975-11-13 1982-12-16 Josef 7120 Bietigheim Blach Screw machine for homogenizing solid, liquid and viscous materials
JPS5386794A (en) * 1976-11-29 1978-07-31 Mitsubishi Gas Chem Co Inc Continuous polymerization
US4136251A (en) * 1977-09-12 1979-01-23 E. I. Du Pont De Nemours And Company Extrusion process for recovery of polymers from their dispersions in liquids

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2537979A1 (en) * 1982-12-21 1984-06-22 Ube Industries PROCESS FOR THE PREPARATION OF FORMALDEHYDE COPOLYMERS
GB2132213A (en) * 1982-12-21 1984-07-04 Ube Industries Preparation of formaldehyde copolymers
EP0198719A2 (en) * 1985-04-17 1986-10-22 Polyplastics Co. Ltd. Method of continuous polymerization and apparatus therefor
EP0198719A3 (en) * 1985-04-17 1988-05-04 Polyplastics Co. Ltd. Method of continuous polymerization and apparatus therefor
FR2647693A1 (en) * 1989-06-02 1990-12-07 Japan Storage Batterie Cy Ltd Device for preparing a paste of active material for a storage battery (accumulator)

Also Published As

Publication number Publication date
CA1184342A (en) 1985-03-19
FR2488896B1 (en) 1985-09-13
NL188290B (en) 1991-12-16
JPS5740520A (en) 1982-03-06
NL188290C (en) 1992-05-18
AU547770B2 (en) 1985-11-07
BR8105183A (en) 1982-04-27
BE890030A (en) 1981-12-16
FR2488896A1 (en) 1982-02-26
DE3132453A1 (en) 1982-06-24
HK85784A (en) 1984-11-16
JPS6213969B2 (en) 1987-03-30
KR840001754B1 (en) 1984-10-19
KR830006334A (en) 1983-09-24
DE3132453C2 (en) 1993-01-14
GB2082597B (en) 1983-11-02
NL8103900A (en) 1982-03-16
AU7437681A (en) 1982-02-25

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Date Code Title Description
PE20 Patent expired after termination of 20 years

Effective date: 20010602