IE42018B1 - Process for the continuous polymerisation of lactams - Google Patents

Process for the continuous polymerisation of lactams

Info

Publication number
IE42018B1
IE42018B1 IE2198/75A IE219875A IE42018B1 IE 42018 B1 IE42018 B1 IE 42018B1 IE 2198/75 A IE2198/75 A IE 2198/75A IE 219875 A IE219875 A IE 219875A IE 42018 B1 IE42018 B1 IE 42018B1
Authority
IE
Ireland
Prior art keywords
plates
webs
mixing
tube
reactor
Prior art date
Application number
IE2198/75A
Other versions
IE42018L (en
Original Assignee
Bayer Ag
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bayer Ag filed Critical Bayer Ag
Publication of IE42018L publication Critical patent/IE42018L/en
Publication of IE42018B1 publication Critical patent/IE42018B1/en

Links

Classifications

    • 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
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/02Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
    • C08G69/08Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
    • C08G69/14Lactams
    • C08G69/16Preparatory processes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01FMIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
    • B01F25/00Flow mixers; Mixers for falling materials, e.g. solid particles
    • B01F25/40Static mixers
    • B01F25/42Static mixers in which the mixing is affected by moving the components jointly in changing directions, e.g. in tubes provided with baffles or obstructions
    • B01F25/43Mixing tubes, e.g. wherein the material is moved in a radial or partly reversed direction
    • B01F25/431Straight mixing tubes with baffles or obstructions that do not cause substantial pressure drop; Baffles therefor
    • B01F25/4316Straight mixing tubes with baffles or obstructions that do not cause substantial pressure drop; Baffles therefor the baffles being flat pieces of material, e.g. intermeshing, fixed to the wall or fixed on a central rod
    • B01F25/43161Straight mixing tubes with baffles or obstructions that do not cause substantial pressure drop; Baffles therefor the baffles being flat pieces of material, e.g. intermeshing, fixed to the wall or fixed on a central rod composed of consecutive sections of flat pieces of material
    • 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
    • B01J19/24Stationary reactors without moving elements inside
    • B01J19/2415Tubular reactors
    • 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
    • B01J19/24Stationary reactors without moving elements inside
    • B01J19/2455Stationary reactors without moving elements inside provoking a loop type movement of the reactants
    • B01J19/246Stationary reactors without moving elements inside provoking a loop type movement of the reactants internally, i.e. the mixture circulating inside the vessel such that the upward stream is separated physically from the downward stream(s)
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00049Controlling or regulating processes
    • B01J2219/00051Controlling the temperature
    • B01J2219/00074Controlling the temperature by indirect heating or cooling employing heat exchange fluids
    • B01J2219/00076Controlling the temperature by indirect heating or cooling employing heat exchange fluids with heat exchange elements inside the reactor
    • B01J2219/00085Plates; Jackets; Cylinders
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00049Controlling or regulating processes
    • B01J2219/00051Controlling the temperature
    • B01J2219/00159Controlling the temperature controlling multiple zones along the direction of flow, e.g. pre-heating and after-cooling
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/18Details relating to the spatial orientation of the reactor
    • B01J2219/185Details relating to the spatial orientation of the reactor vertical
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/19Details relating to the geometry of the reactor
    • B01J2219/194Details relating to the geometry of the reactor round
    • B01J2219/1941Details relating to the geometry of the reactor round circular or disk-shaped
    • B01J2219/1943Details relating to the geometry of the reactor round circular or disk-shaped cylindrical

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Polyamides (AREA)
  • Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The continuous polymerisation of caprolactams using a reactor in which the first 60% of the reactor volume is fitted, at least partly, with static mixing elements. This gives a well-mixed melt at the same time as increased throughput performance.

Description

This invention relates to a process for the continuous preparation of polyamides, preferably from ξ-caprolactam as the main or only monomer, to which, for example, matting agents, colouring agents or light and heat stabilizing substances may be added.
It is known to carry out the continuous polymerisation of polyamides in apparatus of various constructions. In the simplest case, the reactor consists of a simple, vertical tube into which caprolactam, for example, is introduced at the top and from which polymer is removed at the bottom while water is driven off as steam at the top. The desire to control the rate of removal of water in accordance with reaction kinetic considerations has led to the development of multistage tubes, in which the various stages may be telescoped into each other. In the latter case, ascending and descending streams of melt are obtained.
Other devices provided on and in the reactor have the object of imparting a desired temperature profile to the caprolactam which is undergoing polymerisation. This is achieved by simply heating the wall of the reactor or by installing heat exchangers, for example in the form of plates or nests of tubes arranged parallel to the direction ’of flow. It has been found suitable to carry out the .initial phase of the reaction at temperatures above 205°C and the final phase below 250°C, that is to say heat is applied to the top of a VK tube (e.g. the VK process is described in Kunststoffhandbuch Vol. VI, Carl Hauser Verlag Munich (1966) page 191 and removed in the lower part by a suitable heat exchanger. It is important to ensure that cooling sets in only when the conversion of caprolactam, which, as is well known, is a polyaddition reactor, has been substantially completed.
Other developments of the process have the object of ensuring more or less thorough mixing of the caprolactam which is to be polymerised, either in order to stir additives into the caprolactam in the initial phase or in order to obtain a homogeneous melt. The mechanical stirrers of various construction frequently used for this purpose are unsatisfactory, firstly because they are liable to give trouble due to driving and sealing problems and secondly because they do not help to produce the required plug flow. Among the various solutions to overcome this difficulty, it has been proposed to use cascades of stirrer vessels which contribute to the formation of plug flow and the more so the larger the number of vessels arranged in series. This solution, however, resulted in systems which were very complicated and therefore liable to give trouble so that it was not possible to ensure an absolutely constant reaction process which is necessary in order to obtain high quality products.
It is also known to influence the flow in a VK tube by installing various devices in the interior of the tube, for example V-shaped or perforated baffle plates, conical hollow bodies or concentrically arranged annular surfaces extending parallel to the direction of 43018 flow to act as braking surfaces with a view to improving the flow of the melt, but none of these devices has been found to be completely satisfactory.
The iso-called static mixers which have recently become known provide a combination of a mixing action and an action which influences the flow.
It is an object of the.present invention to improve the process for the continuous polymerisation of ε-caprolactam so that not only a thoroughly mixed melt flowing as a plug flow is obtained but also the output is at least 20% higher than can be achieved in prior art processes.
This problem is solved by carrying out the continuous polymerisation of caprolactam in a reactor in which the first 60% of the reactor volume is equipped if possible completely but at least to one-third of this volume with suitable static installations.
According to the invention there is provided a process for the continuous polymerisation of caprolactam 2o in a reactor, wherein at least one-third of the first 60% of the reactor volume is equipped with static mixing installations, the static mixing installations comprising a mixing insert in the form of a pair of plates which have webs defining slots therebetween, the plates being inclined at an angle to each other and to the axis of the reactor tube, and the webs of the two plates either inter-meshing or abutting against each other along edges in the centre of the tube in the form of a gable roof with the ridge of the gable situated perpendicular to the axis of the tubes.
Suitable installations for this purpose are described in Patent Specification No. as stat:*-c devices for the mixing of flowing media.
These reactor tubes contain at least one mixing insert consisting of webs inclined at an angle to each other. In one embodiment, these webs intersect, the inserts consisting of at least two slotted plates set at an angle to each other inside the housing and intermeshing through the slots. In another embodiment, the webs set at an angle to each other do not intersect but contact each other along an edge to form a roof, the ridge of the gable situated perpendicular to the axis of the tube.
As the stream of material encounters the webs, it is split Up into a number of individual streams separated from one another in time and space due to the oblique positioning of the webs On the downstream side of the webs there is a flow gradient in the transverse direction which ensures efficient exchange between the individual streams. Since division of the stream of material into separate streams is staggered in time and space, mixing also takes place in the direction of flow and on this is superimposed radial flow components.
With the transverse mixing which can be achieved it is possible to obtain a good approximation to a plug flow profile so that a narrow spectrum of dwelling times within the reactor can be obtained, which is advantageous for caprolactam polymerisation. The inclination of the webs to the direotion of the oncoming flow and to the wall of the tube may also be in more than one dimension. Additional mixing effects are thereby obtained.
In one particular embodiment, the mixing insert -6-. comprises a plurality of pairs of plates which have a comb-like structure, and the plates are arranged in two rows so -that the webs of at least two plates of one row intersect the webs of at least one plate of the other I row.
Several lines of intersection are thereby produced, a (.ang which the partial streams are further subdivided.
The plates of each row are preferably arranged parallel to each other. This arrangement provides the possibility of more efficient manufacture of the plates.
In a second embodiment, which is particularly advantageous several mixing inserts are provided and the webs of the pairs of plates of the mixing inserts are set at an angle to each other. This angle may be, for example, 90°. With an angle of 90°, the required length of the apparatus is particularly short because the plates of the pairs of plates or the plates of the outer pairs of plates of adjacent mixing inserts can then be pushed far into the gaps between the pairs of plates of the adjacent insert. The relative displacement of the adjacent mixing inserts results in a spaoial subdivision of the individual streams which are produced by the webs. With this embodiment, very powerful mixing effects can be obtained with only a few mixing inserts arranged in a row.
The plates are preferably in the form of combs which have a generally elliptical outline, and in order to improve the flow in the marginal zones of the tube, the web connecting part is shifted from the wall of the tube towards the centre of the tube. In an efficient manufacturing process, this can be achieved by punching 48018 - Ί out. It goes without saying that other manufacturing processes are also suitable for manufacturing the mixing inserts, for example large mixing inserts can be produced by welding. The plates may be constructed,for example, by fixing the webs to a closed ring. The webs and slots are preferably arranged parallel to the main axis Of the plates. This constitutes another advantage with regard to manufacture of the plates.
In various eftibodiments, the webs have a specific cross-sectional profile, for example they may be triangular, tear-shaped or elliptical. Special flow effects which ensure vigorous mixing in the transverse direction, for example, are obtained in the case of a triangular section if one edge is set at an angle to the direction of fLow. The webs may also have a hollow profile. In that ease, they may, for example, be traversed by a heating fluid, so that they also perform a heat transfer function.
If it is desired to vary the velocity of flow of the medium at the centre of the tube as compared with the wall, it is advantageous to vary the width of the webs. The flow is then displaced further towards the centre or.towards the periphery according to whether the webs are wider or narrower towards the centre or the periphery.
The various possible variations of the apparatus for carrying out continuous caprolactam polymerisation afford the constructional engineer wide space for optimising the apparatus. In particular, the. mixing inserts can be constructed from variously formed webs, or variously formed mixing inserts while similar webs - 8 can be arranged behind one another in a suitable sequence. In this way it is possible to adapt the mixing inserts to particular operating factors such as the flow velocity, the viscosity and the residence time of the reactions in the various sections.
Various embodiments of apparatus suitable for practising the. invention are shown purely diagrammatically in the accompanying drawings and described below.
Figures 1 to 5 represent various constructional 10 examples of an apparatus with different arrangements of the mixing inserts or plates and are taken from Patent Specification No. 3^4/6^, wherein they are Figures 14 to 18, Figure 6 shows an example in which the webs do not 15 intermesh and Figures 7 to 10 show diagrammatically reaction tubes for carrying out the process according to the invention.
In Figures 1 to 6, similar parts have been indica20 ted by reference numerals having the same digits in the unit place preceded by a digit representing the number of the figure.
Figure 1 shows several mixing inserts 12 arranged behind one another at angles of 90° to each other inside 'a tube 11, The mixing inserts are formed by intermeshing comb-like plates.
Figure 2 shows mixing inserts 22 arranged in a tube 21. Each insert consists of five pairs of plates 23, 23'. The mixing inserts 22 are displaced by an angle of 90° relative to each other. Plates 23, 23' have the same configuration as in Figure 1.
The mixing inserts 32 arranged in tube 31 in Figure 3 are similar in form to those shown in Figure 2 but in'' addition the oblique webs are inclined to their longitudinal axis.
Figure,4 shows a tube 41 containing mixing inserts 42 which are continuous with each other in that the plates 43,'43' in each case extend through several intersecting plates. The plates are arranged so that there are always two parallel plates of 43 and 43' set close to each other while the distance between these two plates and the next following two plates is about twice as great as the distance of the first two plates from each other.
In the embodiment shown in Figure 5, a tube 51 contains mixing inserts 52 in which plates 53, 53' intersect not only each other but also the plates of adjacent mixing inserts 52, as in the example shown ih Figure 4, so that individual mixing inserts cannot be exactly defined, in this embodiment, importance is attached to the lines of intersection being spaced from the central axis of the tube 51.
Alternatively, the lines of intersection may be dispensed with as in the apparatus shown in Figure 6, and the individual webs may be connected along their edges to form V-shaped inserts. In this apparatus, all the adjacent layers of webs may be displaced from each other in any way desired.
Figures 7 to 10 show diagrammatically reaction tubes for carrying out the process according to the invention. Similar parts have again been indicated by the same unit digits preceded by the number of the figure. 71, 81 91 and 101 indicate the lactam supply, 72 82, 92, and 102 indicate a condenser. The reaotion tubes 73, 83, 93 and 103 are equipped with static installations 74, 84, 94, and 104. In Figure 9, a hydrolysis apparatus 97 equipped with a stirrer 95 is attached to the Upstream end of the reaction tube. In Figure 8, a stirrer 85 is provided inside the reaction tube. In this case, the lactam is preheated at 86.
It will, of course, only be possible to apply the previously described apparatus in accordance with the invention in cases where the stirrer or heat exchanger does not take up the entire volume of the reactor. It is, of course, possible and in many cases advisable, in the interests of obtaining a homogeneous melt with a plug flow to instal static units also in the last 40% of the reactor volume, but this is not necessary for the purpose of the invention. On the other hand, it would be quite insufficient for the purpose of the invention to equip only the last 40% of the reactor volume with these installations.
Known packing mixers, Sulzer-mixers, (Trade Mark) which consists of a first plurality of parallel channels intersecting with a second plurality of parallel channels open to each other on one side are also suitable for carrying out caprolactam polymerisation in accordance with the invention, although for tubes of large diameter, in the case described here of the order of up to 1500 mm, these mixers are not sufficiently economical owing to the manufacturing costs and the high cost of thin sheet metal. Moreover, the pressure drop depends to a very great extent on the selected geometrical configuration of the channel, which is in some cases disadvantage©4301s us.
Static mixers which have to be very long in order to achieve a good mixing effect, for example the Kenies—mixer, (Trade Mark) consisting of a combination of alternately left-handed and right-handed helical elements, cannot be used in the process of the invention, because of the big diameters of VK-tubes. For special constructions, e.g. by dividing the cross section of big VK-tubes into many parallel tubes of smaller diameters, this mixing unit could be suitable for carrying out caprolactam polymerisation, but with high costs of construction.
The effect of the present invention is illustrated by a comparison of the extract values of a polycaprolactam Which has been obtained in a conventional polymerisation tube in Example A with those of a polycaprolactam which has been obtained according to Example B in a tube which is completely identical with the tube used in Example A but in addition is equipped with static mixers as required by the invention. The quantities of chain regulator and water and the reaction temperatures employed are also identical in the two cases. The lactam output from reactor A is 11.0 tons per day and from reactor B 12.1 tons per day. The extract values were obtained by the methanol method. ι 43018 Polymerisation tube A 11,0 tons per day output extract by weight Polymerisation tube 12.1 tons per day output extract by weight 5 11.95% 9.54% 12.01% 9.84% 12.28% 9.11% 12.00% 9.85% 11.90% 9.78% 10 11.92% 9.99% 1?.21% 9.23% For kinetic reasons, caprolactam conversions of 90% and more can be achieved in hydrolytic caprolactam polymerisation. It is clear that this conversion can easily be achieved in a reaction tube B operated in accordance with the invention whereas the conversion rate in the normal reactor is in the region of 88% although the caprolactam output is about 10% lower.

Claims (5)

1. CLAIMS:1. A process for the continuous polymerisation of caprolactam in a reactor, wherein at least onethird of the first 60% of the reactor volume is equipped with static mixing installations, the static mixing installations comprising a mixing insert in the form of a pair of plates which have webs defining slots therebetween, the plates being inclined at an angle to each other and to the axis of the reactor tube, and the webs of the two plates either intermeshing or abutting against each other along their edges in the centre of the tube in the form of a gable roof with the ridge of the gable situated perpendicular to the axis of the tubes.
2. A process as claimed in claim 1, wherein the static mixing installations comprising a mixing insert compris several comb-like pairs of plates, the plates being arranged in two rows so that the webs of two plates of one tow intersect the webs of at least one plate of the other row.
3. A process as claimed in claim 3, wherein the plates of each row are parallel to each other.
4. A process as claimed in any of claims 1 to 3, wherein the webs have a hollow cross-section through which a heating medium is passed.
5. A process as claimed in claim 1 for the con- * tinuous polymerisation of caprolactam substantially as herein described.
IE2198/75A 1974-10-09 1975-10-08 Process for the continuous polymerisation of lactams IE42018B1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE2448100A DE2448100C3 (en) 1974-10-09 1974-10-09 Process for continuous caprolactam polymerization

Publications (2)

Publication Number Publication Date
IE42018L IE42018L (en) 1976-04-09
IE42018B1 true IE42018B1 (en) 1980-05-21

Family

ID=5927884

Family Applications (1)

Application Number Title Priority Date Filing Date
IE2198/75A IE42018B1 (en) 1974-10-09 1975-10-08 Process for the continuous polymerisation of lactams

Country Status (13)

Country Link
JP (1) JPS5833245B2 (en)
BE (1) BE834311A (en)
CA (1) CA1064645A (en)
CH (1) CH625813A5 (en)
DE (1) DE2448100C3 (en)
DK (1) DK453775A (en)
ES (1) ES441583A1 (en)
FR (1) FR2287464A1 (en)
GB (1) GB1523311A (en)
IE (1) IE42018B1 (en)
IT (1) IT1043188B (en)
LU (1) LU73537A1 (en)
NL (1) NL7511814A (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2522106C3 (en) * 1975-05-17 1982-04-15 Bayer Ag, 5090 Leverkusen Device for the continuous mixing of flowable substances and method for producing a mixing insert
DE2808854C2 (en) * 1977-05-31 1986-05-28 Gebrüder Sulzer AG, 8401 Winterthur Flow channel provided with internals for a medium involved in an indirect exchange, in particular heat exchange
JPS60141245U (en) * 1984-02-29 1985-09-19 京セラ株式会社 thermal printing equipment
JPS6120757A (en) * 1984-07-09 1986-01-29 Canon Inc Thermal recording apparatus
SI2764912T1 (en) * 2013-02-08 2018-06-29 Uhde Inventa-Fischer Gmbh Reactor with vertical condensing tube and process for the polymerisation of polyamides in such a reactor

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DD49346A (en) *
NL300045A (en) * 1963-11-01
US3470912A (en) * 1966-11-30 1969-10-07 Du Pont Flow inverter

Also Published As

Publication number Publication date
CA1064645A (en) 1979-10-16
DE2448100C3 (en) 1985-06-20
CH625813A5 (en) 1981-10-15
DK453775A (en) 1976-04-10
BE834311A (en) 1976-04-08
FR2287464A1 (en) 1976-05-07
NL7511814A (en) 1976-04-13
DE2448100B2 (en) 1980-10-09
ES441583A1 (en) 1977-04-01
FR2287464B1 (en) 1980-02-22
GB1523311A (en) 1978-08-31
IT1043188B (en) 1980-02-20
JPS5164598A (en) 1976-06-04
IE42018L (en) 1976-04-09
DE2448100A1 (en) 1976-07-22
LU73537A1 (en) 1976-08-19
JPS5833245B2 (en) 1983-07-19

Similar Documents

Publication Publication Date Title
US6027241A (en) Multi viscosity mixing apparatus
US3362793A (en) Back flow-preventing reactor for continuous polymerization
US6555629B1 (en) Method and device for continuous production of polymers
US4985208A (en) Polymerization reaction apparatus
EP0260736B1 (en) A method of mixing two or more gas flows
US4145520A (en) Process for the continuous polymerization of lactams with static mixers
US7287899B2 (en) Method for continuously and dynamically mixing at least two fluids, and micromixer
US6412975B1 (en) Static mixer
DE2719967A1 (en) CONTINUOUS PROCEDURE FOR CARRYING OUT SUBSTANCE TRANSPORT-RELATED REACTIONS
US6334985B1 (en) Static mixing reactor for uniform reactant temperatures and concentrations
IE42018B1 (en) Process for the continuous polymerisation of lactams
CN102675619B (en) Polymerization reaction device for producing aromatic polycarbonate by melting transesterification method
CN113967454A (en) Device and method for high-selectivity continuous synthesis of mixed dinitrobenzene
US20230219046A1 (en) Apparatus for supplying or dissipating heat, for carrying out reactions and for mixing and dispersing flowing media
JP3225939U (en) Network heat exchange device, network heat exchange method and use thereof
JPH0113726B2 (en)
US3311457A (en) Liquid cascade reactor
CN1154974A (en) Raw-silastic continuously polymerizing apparatus and technology thereof
EP0123653A1 (en) Static heat exchanger with high efficiency in particular suitable for the cooling of viscous fluids
SU1178477A1 (en) Reactor
JPS606412Y2 (en) High viscosity substance processing equipment
SU1667916A1 (en) Mixer for viscous liquids
SU606611A1 (en) Apparatus for conducting heat-exchange reactions in liquid phase
JPH09141085A (en) Cylindrical thin film reaction device
SU1212532A1 (en) Static mixer