GB2046121A - Method and Apparatus for the Recovery of the Solid Material Content of Solutions and/or Suspensions as Granules in Gas Fluidized Bed - Google Patents
Method and Apparatus for the Recovery of the Solid Material Content of Solutions and/or Suspensions as Granules in Gas Fluidized Bed Download PDFInfo
- Publication number
- GB2046121A GB2046121A GB8006837A GB8006837A GB2046121A GB 2046121 A GB2046121 A GB 2046121A GB 8006837 A GB8006837 A GB 8006837A GB 8006837 A GB8006837 A GB 8006837A GB 2046121 A GB2046121 A GB 2046121A
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- United Kingdom
- Prior art keywords
- slit
- fluidized bed
- bed
- grinding surface
- rollers
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Links
- 239000000725 suspension Substances 0.000 title claims abstract description 31
- 239000011343 solid material Substances 0.000 title claims abstract description 26
- 239000008187 granular material Substances 0.000 title claims abstract description 18
- 238000000034 method Methods 0.000 title claims description 44
- 238000011084 recovery Methods 0.000 title claims description 10
- 239000002245 particle Substances 0.000 claims abstract description 106
- 238000000227 grinding Methods 0.000 claims abstract description 47
- 238000009826 distribution Methods 0.000 claims abstract description 27
- 239000011236 particulate material Substances 0.000 claims abstract description 17
- 230000000694 effects Effects 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims abstract description 5
- 238000005243 fluidization Methods 0.000 claims description 26
- 239000007788 liquid Substances 0.000 claims description 12
- 238000007667 floating Methods 0.000 claims description 4
- 238000005507 spraying Methods 0.000 claims description 3
- 230000009471 action Effects 0.000 claims description 2
- 238000006073 displacement reaction Methods 0.000 claims 1
- 238000012423 maintenance Methods 0.000 claims 1
- 239000007787 solid Substances 0.000 abstract description 6
- 239000007791 liquid phase Substances 0.000 abstract 1
- 238000005096 rolling process Methods 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 31
- 230000008569 process Effects 0.000 description 13
- 239000000047 product Substances 0.000 description 12
- 239000000463 material Substances 0.000 description 11
- 238000013461 design Methods 0.000 description 9
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
- 238000005516 engineering process Methods 0.000 description 8
- 238000001694 spray drying Methods 0.000 description 8
- 239000000428 dust Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 230000003247 decreasing effect Effects 0.000 description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 5
- 239000004202 carbamide Substances 0.000 description 5
- 230000000593 degrading effect Effects 0.000 description 5
- 238000005469 granulation Methods 0.000 description 5
- 230000033001 locomotion Effects 0.000 description 5
- 238000005029 sieve analysis Methods 0.000 description 5
- 238000002425 crystallisation Methods 0.000 description 4
- 230000003179 granulation Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000005201 scrubbing Methods 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 3
- 229930006000 Sucrose Natural products 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 235000013681 dietary sucrose Nutrition 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 229960004793 sucrose Drugs 0.000 description 3
- 230000001276 controlling effect Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000005194 fractionation Methods 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000012265 solid product Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 241000256251 Spodoptera frugiperda Species 0.000 description 1
- 235000009470 Theobroma cacao Nutrition 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 235000010633 broth Nutrition 0.000 description 1
- 244000240602 cacao Species 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000013080 microcrystalline material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000003186 pharmaceutical solution Substances 0.000 description 1
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical class C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- CMXPERZAMAQXSF-UHFFFAOYSA-M sodium;1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate;1,8-dihydroxyanthracene-9,10-dione Chemical compound [Na+].O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=CC=C2O.CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC CMXPERZAMAQXSF-UHFFFAOYSA-M 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C13—SUGAR INDUSTRY
- C13B—PRODUCTION OF SUCROSE; APPARATUS SPECIALLY ADAPTED THEREFOR
- C13B30/00—Crystallisation; Crystallising apparatus; Separating crystals from mother liquors ; Evaporating or boiling sugar juice
- C13B30/02—Crystallisation; Crystallising apparatus
- C13B30/028—Crystallisation; Crystallising apparatus obtaining sugar crystals by drying sugar syrup or sugar juice, e.g. spray-crystallisation
-
- 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
- B01J2/00—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic
- B01J2/16—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic by suspending the powder material in a gas, e.g. in fluidised beds or as a falling curtain
-
- 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
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/18—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
- B01J8/24—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique
- B01J8/38—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique with fluidised bed containing a rotatable device or being subject to rotation or to a circulatory movement, i.e. leaving a vessel and subsequently re-entering it
- B01J8/382—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique with fluidised bed containing a rotatable device or being subject to rotation or to a circulatory movement, i.e. leaving a vessel and subsequently re-entering it with a rotatable device only
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Crystallography & Structural Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Disintegrating Or Milling (AREA)
- Glanulating (AREA)
- Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
Abstract
The solids content of solutions and/or suspensions is recovered as granules in a gas fluidized bed which contains particles, the composition of which is identical with that of the solid material in the solution and/or suspension to be processed, in which bed the solution and/or suspension is sprayed on the surface and/or interior of the hot gas fluidized layer, and from which bed particulate material is continuously withdrawn at a mass flow rate corresponding to the solids content of the liquid phase sprayed in, and also, in which bed a grinding effect is created by forcing continuously particles formed in the bed through at least one slit of controllable clearance, located in the fluidized layer itself, in order to produce in a single step, in a single apparatus particulate material of predetermined particle size distribution. The apparatus disclosed has in the fluidized layer a slit-forming device consisting of free rolling rollers and a grinding surface, said rollers being periodically rotated with respect to the grinding surface. <IMAGE>
Description
SPECIFICATION
Method and Apparatus for the Recovery of the
Solid Material Content of Solutions and/or
Suspensions as Granules in Gas Fluidized Bed
This invention relates to a method and apparatus for the removal of the solid material content of solutions and/or suspensions as granules in a gas fluidized bed,
said method comprising essentially spraying the dissolved and/or suspended material on the surface and/or interior of a hot gas fluidized bed consisting of granules formed of the material to be recovered itself, and also comprising a continuous discharge step whereby the particulate material is removed from the fluidized bed at a mass flow rate corresponding to the dissolved material content of the solution and/or suspensions sprayed into the fluidized bed.The apparatus according to the present invention contains a fluidization compartment, at least one sprayer, at least one solid material feeding means and at least one solid material discharging means.
In general multistep technologies are used to recover the solid material content of solutions and/or suspensions. A minimum of three successive steps are required for the removal of an easy-to-crystallize material from its solutions: crystallization, separation (filtration), drying. If the particle size distribution of the solid product thus obtained does not satisfy or only partially satisfies the requirements, several further steps might be required to complete the technology. Such steps might include, among others, the separation and recirculation to the crystaliizer of the undersize particles (either as dissolved material or as crystallization nuclei) and the grinding of the oversize particles.Frequently, the amount of the undersize fraction is considerable or due to characteristics of the crystallization technology only microcrystalline material can be produced.
Therefore, frequently an additional operation granulation-is required to secure the particle size characteristics required. In the case of dilute solution the crystallisation step is preceded by an evaporation step as well.
Spray-drying is frequently used for the recovery of the total solid content of solutions and/or suspensions which can be sprayed.
However, the particle size of the solid material produced by spray-drying is extremely small (generally, in the 10-400 ,um range) and frequently another step, granulation has to be applied to obtain the desired particle size distribution. Also, spray-drying is economical only with concentrated solutions. Therefore, frequently, a concentration step precedes the spray-drying step proper. Thus, spray-drying is frequently only one of the elements of a successful technological chain.
Naturally, apart from the examples cited above
a number of other technologies are also used for the recovery of dissolved materials. However, most of these technologies consist of many steps.
The same applies to most of the technologies used to recover the solid content of suspensions (such complex methods include, e.g. filtration- drying-grinding or granulation, spray-dryinggranulation, etc.).
Recently, fluidization has been used more frequently for the recovery of the solid material content of solutions or suspensions in the form of granules. This process, unlike the multistep technologies, allows for the continuous production, in a single technological step (in one apparatus), of granules from solutions or suspensions.
Particle formation from solutions or suspensions in a gas fluidized bed (i.e. direct particle formation) occurs as follows. Particulate material is fluidized in a continuous fluidization bed with hot gas. The composition of the particulate material forming the bed is identical with that of the dissolved (or suspended) material.
The solution to be processed is sprayed on the surface of the fluidized layer (or into the fluidized layer itself). The droplets impinge upon the surface of the continuously moving particles. The hot fluidizing gas removes the solvent (or suspending liquid) from the surface of the particles, the solvent vapours leave the system along with the hot fluidizing gas. The solid material content of the solution (suspension) remains in the fluidized bed, sticking to the surface of the particles. The offtake of the particulate material from the apparatus is continuous, its mass rate corresponds to the solid material content of the liquid to be processed.
The analysis of the costs of the direct particle formation process showed that direct particle formation was more economical than spraydrying when the amount of water to be evaporated was less than 580 kg/h. Also, the capital costs of the fluidization apparatus were only half of the spray drying unit. The analysis of equal capacity units showed the space requirements-and correspondingly the extent of the supporting investment (building, structures, etc.) were also much smaller in the case of the fluidization system (Christmann, G., Chem.
Anlagen Verfahren 1, 42-43, 1973; Kaspar, J., Rosch, M. Chem. Ing. Techn:45, 746 739/1 973/). As regards the comparison of the economics of the two processes it should be noted that the particle size distribution of the products obtained by the two different methods is very dissimilar. Additional granulation has to be applied after the spray drying step to get a product with a particle size distribution similar to that of the direct particle formation process. The costs of this additional granulation step were not accounted for in the economical analysis.
The basic precondition of the industrial application of the direct particle formation process is the establishment of steady-state operation conditions, and first of all, the establishment of a steady-state particle size distribution. In the fluidized bed the size of the particles increases continuously as solid material is deposited on them from the solution (suspension). This type of particle growth is called surface layering. At the same time the particles, whose surface is wetted by the liquid sprayed in, agglomerate. This results in a very rapid particle size growth rate. The common principle of all published methods used to achieve a steady-state particle size distribution is based on the observation that the above-mentioned processes can be countered by the continuous introduction of small particles (the so-called base-particles).
In practice the most widespread method is the particle addition method. In the most simple cases part of the granules leaving the apparatus is continuously recirculated into the fluidized bed, either directly (German Patent Specification No. 2 363 334), or after grinding (V. F. Volkov et al,
Khim. Prom. 42, 450-453, 1 966). More advantageously the granules withdrawn from the apparatus are fractionated and only the undersize fraction is returned (N. A. Sahova et al., Khim.
Prom. 44, 446-448, 1966; 49 299-301, 1973; 49, 690--694, 1973; J. Kabrar, M.
Rosvh, Chem. Ing. Tech. 45, 736-739, 1973).
Another method of equal practical importance provides for the grinding of the oversize fraction and this ground material is returned to the fluidized bed (British Patent Specification No.
1,381,480). A known and frequently used method applies the combination of the above two methods, i.e. the undersize fraction is returned directly, the oversize fraction is ground and fractionated, and the undersize fraction obtained here is also returned to the fluidized bed (German
Patent Specification No. 2 263 968 and U.S.
Patent Specification No. 3,475,132).
Another less widespread method achieves the steady-state particle size distribution by making use of the fragmentation caused by the changes of the surface temperature of the particles (0. M.
Todes, Krist. Techn. 7, 729-753, 1 972). The principle of the phenomenon is as follows. The particle from the relatively "dry" zone of the fluidized bed enters the spraying zone where it contacts the sprayed liquid, the temperature of which is much lower than that of the particle.
Thus, the surface of the particle is subjected to a sudden cooling effect. Due to the temperature and heat expansion differences between the surface and the interior of the particles degradation takes place. In certain cases this method alone proved sufficient to maintain a steady-state particle size distribution (V. V.
Koziovskij et al. Khim. Prom. 46,122--123, 1970; S. P. Nalimov et al. Ah Prikl. Khim. 43, 581-586,1970).
Both of the above methods used to achieve a steady-state particle size distribution have serious drawbacks. Various additional feeding devices are required for the particle addition technique, such as e.g. continuous solid particle feeder, continuous and variable grinder, pneumatic or other mechanical transfer units, etc. Nevertheless, the steady-state particle size distribution can be controlled only within a relatively narrow range.
Thus, the process is not suitable for the production of granulated material of changing particle size requirements. Also, the decrease of productivity caused by the recirculation of the solid material should not be neglected either. The rate of the particle size disintegration processes caused by the surface temperature fluctuations is sufficient for a steady-state particle size distribution only at high layertemperatures (180--2500C). This factor significantly restricts the range of materials which can be processed by this method, because components which melt or decompose at this bed temperature or below cannot be recovered. Another disadvantageous feature of the high bed temperature is the high energy consumption and low productivity rate.
The present invention relates to a granulating method and apparatus by which particulate material can be produced from solutions or suspensions in a single continuously operated gas fluidized bed, said method being characterized by a steady-state-and controlled as required particle size distribution, without recourse to additional post-granulation operations such as fractionation, grinding, partial recirculation, etc.
The above technological aim can be realized by applying a method and apparatus which forces the particles floating in the fluidized layer through at least one slit or opening of preselected size, and located in the fluidized layer itself, thereby exerting a mechanical grinding effect. By creating and maintaining a directed relative motion between the particles floating in the fluidized bed and the slit(s) arranged in the fluidized layer of the particles can be forced through the(se) slit(s).
The key principle of the present invention postulates that the base particles required for the establishment and control of the steady-state particle size distribution can be created in the fluidized bed itself by subjecting the particles present in the fluidized layer to a grinding mechanical effect.
In other words, the essence of the present inventon is that the particle size growth processes (surface layering, agglomeration), which take place in the fluidized bed once the solution or suspension to be processed is introduced, can be compensated in the fluidized bed itself, in order to achieve a controlled, steady-state particle size distribution, by creating a special, mechanical grinding effect which can be readily regulated, thereby the maximum particle size and the particle size distribution of the material produced can be controlled within a relative wide range.
Advantageously, the particles formed and floating in the fluidized bed are forced through slit(s) of varying position located in the fluidized layer itself. Advantageously, the relative position of the slit(s) is changed periodically, e.g. by rotation, in a given section of the fluidized bed, advantageously the lower section of the fluidized layer. The particles which enter this portion of the fluidized bed are continuously forced to pass through the(se) slit(s). Correspondingly, particles greater, and in certain cases even smaller, than the opening of the slit(s) are necessarily ground.
The apparatus according to the present invention has at least one slit-forming device inside the fluidized bed within the fluidization itself, said slit-forming device advantageously having at least one degrading element and at least one roller element; advantageously the axis of the or each said roller element being parallel with the degrading element and its distance from it being variable. Advantageously, the surface of the degrading element and/or the roller(s) is rough, e.g. knurled. The nominal value of the distance between the roller(s) and the degrading element is set by the slit-clearance setting means according to the required particle size distribution.
In order to prevent overloading or breakage of the slit system it has a design such that upon exceeding a preset limiting force the clearance between the degrading element and the roller(s) can be temporarily increased. By applying a backfolded plate-agitator the grinding efficiency towards the larger particles can be increased and occasional fluidization irregularities can be avoided.
The advantages of the method and apparatus described in the present invention can be summarized as follows:
Contrary to the known multistep technologies the solid material content of solutions and suspensions can be recovered in a single step in a continuous fluidization apparatus and the granules produced have the physical characteristics (particle size distribution, moisture content) required for the end use.
One of the greatest advantages of the operation is that the steady state physical characteristics (particle size distribution, moisture content) of the solid material produced are controlled and maintained in the fluidization bed itself. There is no need for a post-fluidizating treatment (such as fractionation, grinding, solidmaterial transport and feed, etc.) of the produced granulated material. Therefore, the apparatus used in the process, and especially the operation of the apparatus, is extremely simple.
Simultaneously, the specific productivity of the apparatus increases because there is no need for the partial recirculation of the product, nor for high temperatures. Accordingly, both the capital and the operation costs of the apparatus decrease significantly (accounting for the costs of the grinding element and its motor as well).
The particle size of the product can be reliably controlled by simple means (number and size of the rollers, opening of the slit) over a relatively wide range: 0.2-5.0 mm. The particle size of the product can be continuously changed, even during the run, by decreasing or increasing the rotation speed of the grinding element. The particle size of the main portion (about 90% w/w) of the product granules is in a very narrow range 0.2-0.8,0.6-1.6, 1-2,5 mm, depending on the grinding parameters selected. This feature is extremely advantageous from the point of view of further processing or utilization.
The applicability of the process is not limited by the physical characteristics of the materials to be processed (e.g. by low melting point or decomposition temperature).
The process can be used in a number of fields of chemical and related industries for the production of intermediates and final products.
Such (but by no means limiting) fields of application are, for example the following: recovery of active material from pharmaceutical solutions, preparation of granules ready for final processing, containing both the active component and the carrier; preparation of particulate insecticides and herbicides or end products containing both the active component(s) and the carrier; recovery of enzymes in granulated form from fermentation broths; production of single or multicomponent fertilizer granules; recovery of various inorganic salts; recovery from suspensions in granulated form from the raw materials or mixtures of the raw materials used for the production of telecommunication ceramics; preparation of various food products (e.g. granulated instant cocoa). Naturally, the above list is by no means exclusive or restrictive.
The essence of the method and apparatus of the present invention is further explained below with reference to the drawings enclosed and the non-limiting Examples discussed.
Fig. 1 presents the flowsheet of a form of the apparatus and the advantageous arrangement of the ancillary equipment according to the present invention,
Fig. 2 shows a cross-section of the fluidization cell and the slit-forming device according to the present invention,
Fig. 3 shows a cross-section of another possible form of the slit-forming device,
Fig. 4 shows a cross-section along plane IV
IV in Fig. 3, Fig. 5 presents a cross-section of a square cross-section apparatus along plane IV--IV in Fig.
3,
Fig. 6 shows a cross-section along plane VI
VI in Fig. 2 of a version of the apparatus shown in
Fig. 2 equipped with an additional blade mixer as well.
Fig. 7 shows a cross-section along plane IV
IV in Fig. 3 of the apparatus shown in Fig. 3 equipped with an additional blade mixer as well.
The solid material content of solutions or suspensions can be recovered in steady-state conditions as granules of a given or required particle size distribution by the method disclosed in the present invention as exemplified in Fig. 1. In a cylindrical fluidized bed 1 the fluidized layer of the particulate material 3 is located above a supporting and air distributing plate 2. The chemical composition of the particles present in the layer is identical with that of the solid material to be recovered from the solutions or suspensions. A slit-forming device 4 containing rollers 43 (Fig. 2) is placed in the lower section of fluidized layer 3. The slit-forming device is rotated by a variable speed electric motor 5.Fluidizing air which carries the solvent vapours away is pumped through air filter 6 by fan 7 and after passing heat exchanger 9 it enters the fluidized bed. Air flow rate is controlled by gate valve 8.
Hot air passes air distributor 2 and fluidizes the particulate material forming fluidized layer 3. Air leaving fluidized layer 3 enters conical air-space 10 where its linear velocity decreases. Air is exhausted from the fluidization apparatus via port 11. Dust separation from the exhausted air is achieved in cyclone 12. Dust separated in cyclone 12 is fed back continuously by compartment feeder 1 3 into the fluidized bed. Secondary removal, if required and warranted by environmental pollution regulations, is achieved in a continuous wet-scrubber 14. The scrubbing liquid used in wet scrubber 14 is part of the solution or suspension to be processed. Pump 1 8 delivers this liquid through valve 1 7 into wet scrubber 14.Due to the effects of dust separated from the air and dissolved in the scrubbing liquid as well as the evaporation of the solvent, the concentration of the scrubbing liquid in wet scrubber 14 is higher than that of the incoming liquid. The scrubbing liquid leaving wet scrubber 14 is fed back by pump 20 through valve 1 9 into liquid tank 21 equipped with an agitator. Air leaving wet scrubber 14 is exhausted by fan 1 5 through a controlling gate valve 1 6 into the ambient. The solution or suspension stored in tank 21 is delivered by pump 23 through valve 22 to sprayer 24. The spray emitted by sprayer 24 reaches the surface of fluidized layer 3. Here, upon the effect of hot air, solvent evaporates and the solid material content of the solution or suspension is deposited on the surface of the particles.Particle growth processes (i.e. surface layering and agglomerization) taking place in the fluidized bed can be compensated by slit-forming device 4 in order to achieve the steady-state particle size distribution required. Product
granules are discharged by worm feeder 25
driven by variable speed electromotor 26 into
storage bin 27.
Another possible realization of the present invention is described with reference to Fig. 2.
The fluidization apparatus consists of a vertical, cylindrical fluidization bed 1. Circular supporting and air distributing plate 2 is attached to the lower part of the cell. A main shaft 41 driving slitforming device 4 is verticaliy located at the centre of cylindrical fluidization bed 1. The shaft 41 can be driven either at its lower or upper end. The driving unit has to be constructed in such a
manner that the rotational speed of the shaft 41 can be varied. The aim of slit-forming device 4 is the disintegration of the larger particles which are
preferentially present in the lower section of fluidized bed 3. Therefore, advantageously the
slit-forming unit is placed immediately above
supporting and air distributing plate 2. As
required by the given Operation, slit-forming unit
4 can contain one or more rollers 43.It is,
however, more advantageous to use two rollers
43 or pairs of rollers 43. Rollers 43 are attached
symmetrically to the suitably formed ends of arms 42. This arrangement ensures a symmetrical load on shaft 41. It should be noted that there are possible arrangements of slit-forming device 4 with an odd number of rollers 43 which also result in a symmetrical loading of shaft 41. In the realization of the present invention discussed here rollers 43 at the end of arms 42 are supported in free-running bearings in such a manner that a slit clearance of S is formed between them and the rough, advantageously knurled grinding inner surface of fluidization bed 1. Slit-setting devices 45 allow for the setting of clearance S.
Advantageously, the design of the slit-forming device allows for the change of the clearance around the preset value S depending on the size and rigidity of the particles formed in fluidized bed 3. This feature prevents the deformation or breakage of slit-forming device 4 which is equipped with rollers 43.
During the operation of the above-disclosed apparatus rollers 43 move around a circle, at a distance S away from grinding surface 46, as the result of the rotation of main shaft 41. The mechanical grinding effect is due to the shear and compression forces arising between the advantageously knurled surface of rollers 43 and grinding surfaces 46. Meanwhile, rollers 43 can freely rotate around axles 44. The extent of grinding, and eventually, the steady-state particle size distribution is controlled by the number and size of rollers 43, size of slit opening S and the rotation speed of main shaft 41. The size of slit opening S controls, at the same time, the maximum particle size occurring in the fluidized bed. The solution or suspension is fed in and is evenly distributed on the surface of the fluidized layer by sprayer 24.The product is withdrawn by a mechanical feeder, by worm feeder 25. Worm feeder 25 is attached to the side wall of fluidization bed 1, advantageously at the middle or lower part of fluidized layer 3.
Depending on the location of grinding surfaces 46 the design of the apparatus used for the present invention can take a number of possible forms. In the apparatus shown in Figs. 2 and 6 grinding surface 46 is located around the inner wall of cylindrical fluidization bed 1. In the case of the apparatus shown in Figs. 3, 4 and 5 grinding surface 46 takes the form of a special, rough (e.g.
knurled) annulus located at the plane of supporting and air distributing plate 2. It can also assume the role of supporting and air distributing plate 2 (e.g. a porous metal supporting plate of rough surface). The bigger particles formed in fluidized bed 3 occur mostly in its lower section, in the close vicinity of the supporting plate, so grinding surface 46 located at the plane of supporting and air distributing plate 2 ensures primarily the efficient disintegration of the largest particles. The application of grinding surface 46 in the plane of supporting and air distributing plate 2 allows for the use of not only circular fluidized beds also fluidized beds with square and rectangular cross-sections (cf. Fig. 5).
In the apparatus shown in Figs. 3, 5 and 6, the supporting arms 42 (which are connected in a removable way to main shaft 41 located, advantageously, but not necessarily and exceptionally, at the vertical centre line of fluidization bed) allow for the control of the extent of mechanical stress acting upon the particles present in fluidized layer 3. Rollers 43 have horizontal axles 44 joining the ends of horizontal supporting arms 42, so the latter arms act simultaneously as axles of rollers 43 as well.
Thereby, the distance of rollers 43 measured from main shaft 41, and also the circumferential velocity of rollers 43 can be controlled even at a constant r.p.m. of the main shaft. Furthermore, several rollers of equal or different size can be placed simultaneously on supporting arms 42.
The size of opening S between grinding surface 46 at the plane of supporting and air distributing plate 2 and rollers 43 can be set by slit-opening controlling device 45, which is connected either in a rigid or a flexible manner. The particle size distribution can be controlled by the size of opening S, the r.p.m. of main shaft 41, the magnitude of the area of grinding surface 46, and the number and size of the rollers. Uniform feed and distribution of the solution or suspension takes place via sprayer 24 while product discharge is achieved through mechanical feeder (e.g. worm feeder) 25.
In the apparatus disclosed in the present invention and shown in Figs. 3, 4 and 5 slitforming device 4 is located in the lower section of fluidized layer 3, so it effects primarily the larger particles preferring this section of the layer. The efficiency of the grinding of the larger particles present in the lower section of fluidized bed 3 can be enhanced by installing a mixing element on main shaft 41 immediately above supporting and air distributing plate 2 in such a manner so as to ensure that the larger particles, subjected to a less intense fluidization movement, enter the space between grinding surface 46 and rollers 43. Such solutions are shown in Figs. 6 and 7. The elements already discussed in connection with
Figs. 3, 4 and 5 are designated by the same numbers.
In Fig. 6 grinding surface 46 is located along the internal wall of cylindrical fluidization bed 1.
Backfolded plate agitator 47 located immediately above supporting and air distributing plate 2, and connected via a releasable joint, forces the large particles in the lower section of fluidized layer 3 away from the vertical centre line of cylindrical fluidized bed 1 towards its wall equipped with grinding element 46. This action ensures that the large particles at the bottom of fluidized layer 3 meet grinding rollers 43, and simultaneously, it prevents the development of fluidization irregularities (stagnant layer, channelling) in the lower section of fluidized layer 3.
In Fig. 7 grinding surface 46 is located at the plane of supporting and air distributor plate 2. In this case the role of back-folded plate agitator is to hold the large particles in front of rollers 43 on grinding surface 46, and also to prevent the development of fluidization irregularities.
In order to further explain same points of the present invention some non-limiting and nonrestricting Examples are given below:
Example 1
Particulate sodium chloride is produced from a 250 g/l solution. Into a fluidized bed of 0.3 m inner diameter 1 5 kg particulate sodium chloride is introduced and fluidized with 100 Nm3/h air at 120"C. The rotational speed of the slit-forming device of given size and clearance setting is set at 1 8 r.p.m. The design and location of the slitforming device is the same as shown in Figs. 3 and 4. The sodium chloride solution is sprayed into the fluidized bed at a rate of 5 I/h. Solid material is withdrawn from the fluidized layer at a rate of 1.25 kg/h. The solid material dust (below 0.3 mm particle size) separated in the cyclone is continuously returned.The flow rate of the fluidizing gas is continuously increased up to 1 80 Nn3/h during a period corresponding to the average residence time, some 12 hrs, while air temperature is maintained at 1200C. Generally, steady-state operation conditions could be achieved in this period. The moisture content of the particulate sodium chloride removed from the apparatus is below 0.2 % w/w. The sieve analysis of the product fraction yielded a particle size distribution as follows:
Particle Size, mm Weight % 0.2-0.4 9.0 0.4-0.6 23.1 0.6-0.8 28.1 0.8-1.0 32.1 1.0-1.6 7.7
After a longer steady-state operation period the rotational speed of the slit-forming device was increased to 30 r.p.m.As in the previous case, steady state conditions could be established in 10 hrs. During this period the flow rate of air was decreased from 1 80 Nm3/h to 140 Nm3/h. The moisture content of the particulate material withdrawn from the fluidized bed remained 0.2 % w/w, while the particle size decreased, as shown by the sieve analysis data::
Particle Size, mm Weight % 0.1-0.2 2.9 0.2-0.4 32.0 0.4-0.6 34.2 0.6-0.8 20.2 0.8-1.0 8.1 1.0-1.6 2.6
Example 2
Particulate urea was produced from a 450 g/l solution, 9 kg particulate urea (particle size, 0.6- 0.8 mm) was charged into the fluidizing apparatus (internal column diameter 0.3 m) and fluidized with 80 Nm3/h air at 1000C. The rotational speed of the slit-forming device of given design was set at 12 r.p.m. The design and location of the slit-forming device were identical with those shown in Fig. 2. Urea solution was sprayed into the apparatus at a flow rate of 3 I/h, particulate material was discharged at a mass flow rate of 1.35 kg/h.Dust separated in the cyclones was returned into the apparatus. In a period corresponding to the average residence time of the particulate material (some 6.7 less) the air flow rate (ensuring both the fluidization movement and the removal of the solvent vapours) was increased to 1 60 Nm3/h, while its temperature was maintained at 1000C. The moisture content of the particulate urea discharged from the apparatus was below 0.5 % w/w.
The sieve analysis resulted in:
Particle Size, mm Weight % 0.4-0.6 1.3 0.6-0.8 1.7 0.8-1.0 16.6 1.0-1.6 78.9 1.6-2.5 1.5
After a long steady-state operation period the rotational speed of the slit-forming device was increased to 30 r.p.m. Steady state conditions were achieved again after 6 hrs. In this period the air flow rate was decreased from 1 60 Nm3/h to 120 Nm3/h. The moisture content of the particulate urea product discharged from the apparatus was below 1 % w/w.Its particle size decreased as shown here:
Particle Size, mm Weight % 0.2-0.4 2.1 0.4-0.6 23.3 0.6-0.8 29.5 0.8-1.0 38.7 1.0-1.6 6.4
Example 3
Particulate saccharose was produced from a 700 g/l solution. 12 kg particulate saccharose (particle size 0.6-0.8 mm) was charged into the fluidized bed (inner column diameter 0.3 m) and fluidized with 130 Nm3/h air at 1000C. The rotational speed of the slit-forming devce of given size and design as well as that of the backfolded plate agitator was set at 47 r.p.m. The design and location of both the slit-forming device and the back-folded plate agitator were identical with those shown in Figs. 2 and 6.Saccharose solution was sprayed in at a flow-rate of 3.5 I/h, while the solid product was discharged at a mass flow rate of 2.45 kg/h. Solid dust separated from the discharged air flow was continuously returned into the fluidized bed. In a period corresponding to the average residence time of the particulate material (some 4.9 hrs) the airflow rate (ensuring both the fluidization movement and the removal of the solven vapours) was increased continuously up to 200 Nm3/h, while its temperature was maintained at 1000C. In steadystate conditions the moisture content of the particulate material was below 0.2% w/w, while its particle size distribution was as follows::
Particle Size, mm Weight % 0.2-0.4 0.8 0.4-0.6 7.4 0.6-0.8 1 6.7 0.8-1.0 35.5 1.0-1.6 39.6
After a longer period of steady state operation the rotational speed of the slit-forming device was decreased to 30 r.p.m. New steady state conditions were achieved in 5 hrs. During this period the flow rate of fluidizing air was increased from 200 Nm3/h to 300 Nm3/h.The moisture content of the particulate material discharged in steady-state conditions was below 0.1 % w/w. its particle size increased as shown by sieve analysis:
Particle Size, mm Weight % 0.4-0.6 0.8 0.6-0.8 3.0 0.8-1.0 1 8.5 1.0-1.6 58.5 1.6-2.5 19.2
Example 4
Particulate ferric oxide was produced from a 830 g/l suspension containing 4 g/l organic material as well. 25 kg particulate ferric oxide (particle size 0.4-0.6 mm) was charged into the fluidized bed (inner column diameter 0.3 m) and it was fluidized with 200 Nm3/h air at 130"C. The rotational speed of the slit-forming device of given size and that of the back-folded plate agitator was set at 20 r.p.m. The design and location of both the slit-forming device and the plate agitator were identical with those shown in
Figs. 3 and 7. The suspension was sprayed in at a flow rate of 1 0 I/h, while solid material was discharged at a mass flow rate of 8.34 kg/h. Dust separated from the exhausted air flow was continuously returned into the fluidized bed. In a period of some 3 hrs the air flow rate ensuring both the fluidization movement and the removal of the solvent vapours was continuously increased to 300 Nm3/h. The moisture content of the particulate material discharged under steady state conditions was below 0.5% w/w. Sieve analysis resulted in:
Particle Size, mm Weight %
below 0.2 10.9 0.2-0.4 26.5 0.4-0.6 38.9 0.6-0.8 10.6 0.8-1.0 3.1
Claims (14)
1. Method for the continuous recovery of the solid material content of solutions and/or suspensions in the form of granules of predetermined particle size distribution achieved via the spraying of the solution and/or suspension to be processed on the surface an/or interior of hot gas, and especially hot airfluidized bed composed from particles, the composition of which is identical with that of the solid material content of the solution and/or suspension to be processed, while a continuous discharge of the particulate material takes place at a rate corresponding to the solid material content of the liquid sprayed into the fluidized bed, said method being characterized by the presence of at least one slit of controllable opening (size) through which the particles present, forming and/or growing in the fluidizing bed are forced, thereby creating a continuous, mechanical grinding effect.
2. Method according to claim 1, in which the particles present in the fluidized bed are forced through the slit(s) by the creation and maintenance of directed relative displacement between said slit(s) and the particles.
3. Method according to claim 1 or 2 in which the floating particles formed in the fluidized bed are forced through slit(s) of continuously changing position.
4. Method according to claim 3 in which the position of the slit(s) in the fluidized bed is periodically changed.
5. Method according to any of claims 1 to 4, in which the particles are forced through preselected slit(s) located in the fluidized bed, the clearance of said slit(s) being resiiiently variable to a certain extent.
6. Apparatus for carrying out the method claimed in any of claims 1 to 5, which contains at least a fluidization bed, a sprayer, a solid material feeder and product dischanging unit, said apparatus being characterized by the presence of at least one slit-forming device in the fluidized layer section of the fluidized bed.
7. Apparatus according to claim 6, in which said slit-forming device consists of a grinding surface and at least one roller element having its axis advantageously parallel with grinding surface and its clearance being variable.
8. Apparatus according to claim 7 in which said slit-forming device has a vertically driven main shaft, advantageously entering the system from below, said supporting side arms with at least two rollers swivelling around their own axles located at the end of the supporting arms, and having at least one slit-setting means used to control the distance between the grinding surface and the rollers.
9. Apparatus according to claim 8, in which at least in the section of the fluidized layer there is a cylindrical fluidized bed parallel with main shaft, the inner circumferential surface area of said bed having a grinding surface, while rollers at a distance from said grinding surface controlled individually by said slit-setting means are located in free-running bearings around axles parallel with the longitudinal direction of said grinding surface, located at the end of the supporting arms.
10. Apparatus according to claim 8 in which said grinding surface is formed on a supporting and air distributing plate located in the lower section of the fluidized bed, and in which rollers forming a slit of clearance with said grinding surface are located in free running bearings along axles parallel with the grinding surface (advantageously along a horizontal axis) at the end of supporting arms connected via slitsetting device to main shaft.
11. Apparatus according to any of claims 7 to 10, in which rollers are located on movable axles in order to ensure a temporary increase of preset slit-clearance underthe action of a force exceeding a preset level.
12. Apparatus according to claim 11 in which spring-loaded slit-setting device(s) allow for the temporary, resilient changes of the nominal slitclearance preset between said grinding surface and said rollers.
13. Apparatus according to any of claims 7 to
12, in which the grinding surface and/or the surface(s) of roller(s) are rough, advantageously knurled.
14. Apparatus according to any of claims 8 to 13, in which an additional blade agitator, which rotates together with main shaft is also added on the main shaft in the fluidized layer section.
1 5. A method according to claim 1 substantially as herein described in any one of the
Examples and/or with reference to and as shown in any one of the preferred embodiments illustrated in the drawings.
1 6. Apparatus according to claim 6 substantially as herein described with reference to and as shown in any one of the preferred embodiments illustrated in the drawings.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HUMA003117 HU185004B (en) | 1979-03-03 | 1979-03-03 | Process for separating dry substant content of solutions and/or suspensions and in forme of granulate, and for granulating powders and mixtures of powders in a layer fluidized with gas, and apparatus for the process |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| GB2046121A true GB2046121A (en) | 1980-11-12 |
| GB2046121B GB2046121B (en) | 1983-10-26 |
Family
ID=10999067
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB8006837A Expired GB2046121B (en) | 1979-03-03 | 1980-02-28 | Method and apparatus for the recovery of the solid material content of solutions and/or suspensions as granules in gas fluidized bed |
Country Status (4)
| Country | Link |
|---|---|
| CH (1) | CH645034A5 (en) |
| DE (1) | DE3007292C2 (en) |
| GB (1) | GB2046121B (en) |
| HU (1) | HU185004B (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5580002A (en) * | 1993-08-27 | 1996-12-03 | Bpb Industries Public Limited Company | Method and apparatus for heating and grinding materials |
| EP1640048A4 (en) * | 2003-05-09 | 2008-07-23 | Toto Kasei Kk | PROCESS FOR CRYSTALLIZING AN ORGANIC OLIGOMER, EPOXY RESIN COMPOSITION COMPRISING SAID ORGANIC OLIGOMER, AND CURED EPOXY RESIN MATERIAL |
| EP2932856A1 (en) | 2014-04-07 | 2015-10-21 | Evonik Degussa GmbH | Process for fluidized bed granulation of amino acid-containing fermentation broths |
| EP3315192A1 (en) | 2016-10-27 | 2018-05-02 | YARA International ASA | Fluidized bed granulation |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0093720B1 (en) * | 1981-06-22 | 1985-03-27 | Alfa-Laval Ab | A process for the production of animal feed stuff from a liquid residue obtained by fermentation and distillation of grain raw material |
| DE3248504A1 (en) * | 1982-01-09 | 1983-07-21 | Sandoz-Patent-GmbH, 7850 Lörrach | Process for producing non-dusting granules and apparatus therefor |
| RU2143313C1 (en) * | 1998-10-05 | 1999-12-27 | Государственное предприятие РФ Центральное научно-конструкторское бюро | Installation for granulation of finely divided materials |
| USD510868S1 (en) * | 2003-09-30 | 2005-10-25 | Pamela Rae | Bottle |
| CN112121449A (en) * | 2020-09-22 | 2020-12-25 | 杭州嘉威机械配件有限公司 | Laboratory is with miniature spray drier convenient to remove |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1381505A (en) * | 1971-06-06 | 1975-01-22 | Struthers Scient International | Fluidized bed process and apparatus |
| CH558674A (en) * | 1971-07-01 | 1975-02-14 | Ciba Geigy Ag | METHOD AND DEVICE FOR MANUFACTURING GRANULES. |
| DE2317129C3 (en) * | 1973-04-05 | 1981-11-05 | Glatt, Werner, 7859 Haltingen | Fluidized bed spray granulator |
| DE2418552A1 (en) * | 1973-04-19 | 1974-11-14 | Ciba Geigy Ag | Fluidised bed granulation from liquid - with recycling of large proportion of granulate to keep bed stable |
| DE2341504C3 (en) * | 1973-08-16 | 1978-10-12 | Dr. Karl Thomae Gmbh, 7950 Biberach | Fluidized bed spray granulation method |
| DE2551578A1 (en) * | 1975-11-17 | 1977-05-26 | Werner Glatt | Granulator with rotary stirrer and upright cylindrical vessel - through which drying air flows vertically upwards |
-
1979
- 1979-03-03 HU HUMA003117 patent/HU185004B/en not_active IP Right Cessation
-
1980
- 1980-02-25 CH CH160780A patent/CH645034A5/en not_active IP Right Cessation
- 1980-02-27 DE DE19803007292 patent/DE3007292C2/en not_active Expired
- 1980-02-28 GB GB8006837A patent/GB2046121B/en not_active Expired
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5580002A (en) * | 1993-08-27 | 1996-12-03 | Bpb Industries Public Limited Company | Method and apparatus for heating and grinding materials |
| EP1640048A4 (en) * | 2003-05-09 | 2008-07-23 | Toto Kasei Kk | PROCESS FOR CRYSTALLIZING AN ORGANIC OLIGOMER, EPOXY RESIN COMPOSITION COMPRISING SAID ORGANIC OLIGOMER, AND CURED EPOXY RESIN MATERIAL |
| EP2932856A1 (en) | 2014-04-07 | 2015-10-21 | Evonik Degussa GmbH | Process for fluidized bed granulation of amino acid-containing fermentation broths |
| US9649609B2 (en) | 2014-04-07 | 2017-05-16 | Evonik Degussa Gmbh | Process for fluidized bed granulation of amino acid-containing fermentation broths |
| EP3315192A1 (en) | 2016-10-27 | 2018-05-02 | YARA International ASA | Fluidized bed granulation |
| WO2018078074A1 (en) | 2016-10-27 | 2018-05-03 | Yara International Asa | Fluidized bed granulation |
Also Published As
| Publication number | Publication date |
|---|---|
| CH645034A5 (en) | 1984-09-14 |
| DE3007292A1 (en) | 1980-09-11 |
| HU185004B (en) | 1984-11-28 |
| DE3007292C2 (en) | 1984-07-12 |
| GB2046121B (en) | 1983-10-26 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PCNP | Patent ceased through non-payment of renewal fee |