GB2035365A - Improvements in filtration - Google Patents
Improvements in filtration Download PDFInfo
- Publication number
- GB2035365A GB2035365A GB7932281A GB7932281A GB2035365A GB 2035365 A GB2035365 A GB 2035365A GB 7932281 A GB7932281 A GB 7932281A GB 7932281 A GB7932281 A GB 7932281A GB 2035365 A GB2035365 A GB 2035365A
- Authority
- GB
- United Kingdom
- Prior art keywords
- coal
- filter
- aid
- filter cake
- product
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000001914 filtration Methods 0.000 title claims abstract description 34
- 239000003245 coal Substances 0.000 claims abstract description 88
- 239000012065 filter cake Substances 0.000 claims abstract description 42
- 238000000034 method Methods 0.000 claims abstract description 25
- 239000002904 solvent Substances 0.000 claims abstract description 21
- 238000000605 extraction Methods 0.000 claims abstract description 17
- 239000007788 liquid Substances 0.000 claims abstract description 12
- 238000012545 processing Methods 0.000 claims abstract description 10
- 239000000284 extract Substances 0.000 claims description 29
- 239000002245 particle Substances 0.000 claims description 21
- 239000000047 product Substances 0.000 claims description 12
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 10
- 239000011707 mineral Substances 0.000 claims description 10
- 238000002485 combustion reaction Methods 0.000 claims description 9
- 239000003039 volatile agent Substances 0.000 claims description 6
- 238000004513 sizing Methods 0.000 claims description 2
- 239000000463 material Substances 0.000 abstract description 4
- 239000002956 ash Substances 0.000 description 28
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 14
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
- 239000000706 filtrate Substances 0.000 description 11
- 239000008188 pellet Substances 0.000 description 10
- 238000012360 testing method Methods 0.000 description 9
- 239000007787 solid Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 6
- 239000005909 Kieselgur Substances 0.000 description 5
- 238000000926 separation method Methods 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 238000004380 ashing Methods 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- 239000002802 bituminous coal Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000003575 carbonaceous material Substances 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 239000010881 fly ash Substances 0.000 description 2
- 238000002309 gasification Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000013019 agitation Methods 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 238000004939 coking Methods 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 239000003208 petroleum 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
- 238000002360 preparation method Methods 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000005549 size reduction Methods 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- 239000002641 tar oil Substances 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002918 waste heat Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G1/00—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
- C10G1/04—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by extraction
- C10G1/045—Separation of insoluble materials
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Filtering Materials (AREA)
Abstract
In the extraction of coal using a liquid solvent oil, filtration of the residual material can be assisted by using a filter aid which is of coal origin. The filter aid is produced by high temperature processing of coal or of an ash-rich coal-derived residue, and is conveniently made from filter cake from the process.
Description
SPECIFICATION
Improvements in filtration
This invention concerns the filtration of coal extract, and more especially concerns the use of filter aid in the improvement of filtration of coal extracted using liquid solvents.
It is well known in the art that bituminous coal can be extracted to varying degrees using a high boiling aromatic solvent. The solvent may be highly aromatic petroleum fraction or more usually an oil derived from coal, e.g. a coal tar fraction such as anthracene oil. The extract consists of coal substance in solution and solids mainly comprisng mineral matter (ash) from the coal, together with a proportion of undissolved carbonaceous material. An important step in further processing is the separation of the solids and a variety of methods have been proposed or used, none of which are entirely satisfactory. The present invention is concerned with the use of filtration as a separation method.Filtration of coal extracts tends to be slow because of a number of factors including the high viscosity of filtrate, filter cakes which are at least partly compressible, and the very fine suspended particles.
It has now been discovered that conventional filter aids such as diatomaceous earth for example those marketed under the trade name "Celite" by Johns-Manville Corp., are effective when added as body aid in increasing the filter rate of coal extract and decreasing the filter cake resistivity. An important factor in the overall economics of the liquid extraction of coal is the cost of filtration and the value of the filter cake which is discarded. If the filte cake is used as a fuel, e.g. in power stations, then the addition of diatomaceous earth lowers the calorific value of the cake; in addition, the diatomaceous earth costs about 200 per tone at 1978 prices and is discarded with the cake.
Filter aids are divided into two major types, namely body aid and precoat. A body aid is added to the suspension to be filtered, and increases the porosity of the filter cake in order to yield a more rapid filtration.
A precoat is applied to a filter by deposition from suspension, before filtration of the suspension to be filtered, and acts to form a filtration medium which is a more effective filter than the filter cloth or gauze itself.
The present inventors considered the use of ground coal as a body aid but this produced small improvements only in tests. To their surprise, however, it was found that the heat treatment of coal or carbonaceous ash-rich coal-derived residue yields excellent filter aids comparable with diatomaceous earth.
In particular it was found that excellent filter aids could be produced from the filter cake of a coal extraction process.
The invention therefore also provides a method of filtering coal extract resulting from the extraction of coal with a liquid solvent using a filter aid which is the product of high temperature processing of coal or an ash-rich coal derived residue under conditions at which the ash component of the coal or residue does not fuse and volatiles are removed therefrom.
The residue may be filter cake from the filtration of coal extract, which offers the possibility of an integrated coal extraction process which produces its own requirement of filter aid.
The invention, in a first embodiment, comprises the use, as body aid or as precoatfilter aid, of ash produced by the combustion of coal or residue, under conditions at which the mineral matter (ash) in the coal or residue does not fuse.
A particularly preferred filter aid is that produced from filter cake, that is, the ash from burning filter cake.
However, other products of combustion, for example ash from fluidised combustion of coal such as the ash separated in the cyclones cleaning the combustion gases of such a process, or ash from the combustion of residues from coal preparation plant may be used as filter aid according to the invention.
Optionally, in the case of ashing filter cake, solvent oil may be recovered by evaporation from the filter cake before the combustion of the dried filter cake under conditions at which the mineral matter in the cake does not fuse and the collection of the ash from such combustion for use as said filter aid. Before further processing, the filter cake may be extruded into pellets or otherwise pelletised. The step of solvent recovery is optional, and is intended for use in processes in which there is no efficient step of washing and drying the filter cake in the filter, that is in a process in which a substantial proportion of solvent remains in the filter cake.
Tests on the ash have shown that it is effective both as a body aid, and as a precoat. The method disclosed of producing filter aid permits the production of ash particles which are porous and of relatively large particle size ( > 1.00 mm), which are especially suitable as a precoat.
The combustion temperature is preferably in the region 600 to 9500C, e.g. 800 to 950"C.
The filter aid may be used as a body aid according to the invention at a concentration of 0.5 - 2% by weight, preferably about 1% by weight, in the suspension, and as a precoat at a concentration of 5-20%, preferably about 10% by weight, in solvent or in filtrate. Conveniently, for use as a precoat, the filter aid is mixed with suitable solvent then applied to the filter as a slurry. The slurry may contain other components, such as small quantities of asbestos fibres to give extra strength to the precoat.
The invention, in a second embodiment, comprises the use as a precaot filter aid of ash-rich coal-derived residue which has been heat treated to substantially remove volatiles and any liquid solvent present.
Preferably, the coal-derived residue is filter cake from the liquid extraction of coal, although other residues, e.g. from gravity settling, centrifugal separation or the like, may be used. The liquid extraction of coal is, as has been stated, well known in the art, and may be conveniently effected using an aromatic solvent oil such as a tar oil, preferably anthracene oil, and may be in the presence or absence of hydrogen.
Preferably, when the residue is filter cake from coal extraction, the cake is extruded into pellets or is otherwise pelletised. The resulting pellets are then heat-treated, preferably at a temperature of approximately 600"C until the solvent and any other volatiles are driven off, that is suitably for a period of 6 to 30 minutes.
The heat-treated pellets are particularly useful as a precoat filter aid and will be described specifically as such hereinafter. They are crushed and/or ground to a particle size dependent upon the screen size of the filter.
The particles should not be large monosize particles which would produce a precoat with large voids which would not retain the small residual particles in the extract and would result in poor filtrate clarity (a high solids content in the filtrate). Thus the precoat must contain at least a proportion of material with a size sufficient to bridge the filter screen, and, for example, suitable particle sizes are for a 200 um woven wire mesh screen are less than 425 ijm.
As has been indicated, solvent oil and other volatiles are collected from the heat-treatment. As well as the recovery of solvent, in the case of hydrogenated extracts it is envisaged that low boiling olefins which are valuable chemical feedstocks can also be collected.
Only a proportion of the total filter cake in a coal extraction process will be required as precoat filter aid. All the filter cake may be pelletised and heat-treated in the same way, the proportion required for filter aid being crushed to the appropriate size, and the remainder being gasified to produce hydrogen in manner known per se. Because of the heat-treatment, the material to be gasified is "cleaner" than most conventional feeds for gasification. That is, despite its high ash content, the yield of troublesome tar material evolved during gasification is relatively low.
Commercial precoat filter aids are availabie from various sources; the present invention offers a significant cost saving compared to "Celite" and "Perlite" filter aids.
It will be appreciated that the method of the invention offers the possibility of a coal extraction process self-sufficient in precoat. The method of the invention is contrary to prior views on the de-ashing of coal extracts; de-ashing is well known to be an expensive and troublesome part of a coal extraction process and the invention amounts to the recycling of ash to the upstream side of the filter. The present filter aid is usable at concentrations and in the manner described above in the description of the first embodiment.
The invention therefore also provides a method of extracting coal, comprising digesting coal in a liquid solvent oil and filtering the undissolved coal and mineral matter from the extract, wherein filter cake from the filtration steps is heat-treated to substantially remove volatiles and any liquid solvent present under conditions at which the mineral matter does not fuse, sized to an effective filter aid particle size and the product used as a filter aid in the next cycle of filter operation.
Preferably, the products used according to the invention as filter aids are sized to an effective filter aid particle size. The sizing may be carried out by screening and, if necessary, grinding or other size reduction.
The invention will now be described by way of example and with reference to the accompanying drawings, in which
Figure 1 illustrates graphically the filtration rates of coal extract without filter aid, and with various body aids,
Figure 2 is a schematic diagram of a plant to make filter aid from coal extraction filter cake.
Example 1
a) A coal extract was prepared on a 1/2 tonne per day continuous pilot plant, by extracting a sample of
Beynon coal (a prime coking coal, coal rank code [CRC] 301 a in the National Coal Board's Coal Classification "The Coal Classification System used by the National Coal Board (Revision of 1964)", published by National
Coal Board Scientific Control, London) with 4 times its weight of anthracene oil, at 420"C for a residence time of 1 hour. Accurately weighed amounts of filter aid were added to samples of the coat extract, as body aid.
The mixture was well stirred, filtered at 1.38 x 105 Pa (20 psi) pressure through a heated (225"C) filter and the filtration rate data recorded. The filtration temperature was kept constant for the series of tests since preliminary work had shown small but unexplained changes in cake resistivity with temperature.
b) A series of tests to determine flow rate were carried out using test samples: "A" 1% ash prepared from filter cake, in the coal extract. The ash was prepared by heating a sample of filter cake from filtering an extract of a mid rank coal in anthracene oil, to 950 C in a furnace in the presence of air.
"B" 1% "Celite" 505 commercial diatomaceous earth filter aid, in coal extract.
"C" 1% Secondary ash fines recovered from the cyclone separation of a five foot (1.52 m) diameter fluidised bed coal combustor, in coal extract.
"D" 1% power station fly ash (Central Electricity Generating Board), in coal extract.
"E" Coal extract without filter aid.
"F" 1% First ash fines from the five footfluidised coal combustor, in coal extract.
Filter cake resistivity was calculated but can be misinterpreted when filtering using body aids, so that for many practical purposes the filtration rate is more useful. The general equation for flow per unit filtering area is
f = atb where a and bare constants,
f represents total flow per unit area
t represents time.
It follows that a logarithmic plot of total flow against time should produce a straight line which will serve as a rate plot. This was done forthe samples "A" to "F" and is illustrated in Figure 1, which shows total flow in g against time in mins.
c) All the types of ash reduced the filter cake resistivity and increased the filtration rate. The ash from filter cake and the secondary fines from the fluidised bed combustor were especially effective, the former being comparable in performance with the commercial filter aid.
The performance of body aids appears to be dependent on the particle structure and size. The CEGB fly ash is composed mainly of solid spheres and is a poor body aid when compared with the irregular open structure of the ash produced from filter cake. These structures are largely determined by the temperature at which the ash was formed; ash produced above its fusion temperature has been found to form a poor body aid.
d) In a further test, coal from Penailta colliery (a CRC 202 high rank coal) was ground to 100% - 200 Cim.
This coal was selected on the basis that it does not swell or sofen at the filtration temperature. The addition of this ground coal to coal extract as a filter body aid reduced the filter cake resistivity whilst producing a small improvement in filtration rate. The reduction in filter cake resistivity is a result of the increased solids loading and the overall indications are that coal perse does not have the correct particle structure to function as a body aid.
Example 2
a) When assessing the filter aid as a precoat, the assessment is based mainly on filtrate clarity rather than on filtration rate. The precoat tests were carried out using wire mesh (100 m and 0.4 mm) in place of the filter paper used in the body aid tests. The precoat was applied as a slurry of 10% by weight in anthracene oil immediately prior to the filtration of the extract. The filtrate was collected as aliquots and these were analysed for ash content. The filtration rate was recorded, and the results of the precoat tests are given in the table below.
Wire mesh size 100Ftm 100 julm 0.4 mm precoat Paper Celite Filter aid Filter aid
560 from cake (3) from cake (3) % Conc. of residual - 0.35 0.60 1.63 filter aid in (1) application solution
% Filtrate ash (2) 0.06 0.09 0.08 0.15 (@ steady conditions)
Filter cake resistivity 2.3 3.7 3.2 m kg~1 x 10.11 Filtration rate 2.85 3.0 3.0 @109(9minl) Notes: (1) Residual content of precoat in precoat solution after applying precoat (initially 10%)
(2) Neglecting first filtrate formed (nominally 20%} (3) The filter aid is prepared fom the filter cake mentioned in sample A of Ex. 1, but extruded into
pellets before heat treatment at 950"C.
b) The results in the table show that the clarity of the filtrate and the filtration rate obtained with a precoat of filter aid prepared from filter cake was comparable with a "Celite" precoat. The filter aid prepared from filter cake was abie to bridge gaps of up to 0.4 mm, despite the filter aid only containing particles up to 100 micron.
c) It was found that if the filter aid is prepared from pieces of filter cake, without extrusion some large particles ( > 1.00 mm) remained after heat treatment and these were not destroyed by agitation. The large particles were comparable in performance as a body aid with smaller particles ( < 1.00 mm), which implies that the large particles must be porous in character. Such large particles are therefore indicated especially for use as precoats because of their large size and high porosity.
Figure 2, as has been stated, illustrates a scheme for the production of filter aid from filter cake from a coal extraction process. The filter cake, stream A, is removed from the filter, 1, then passed through an extruder, 2, to yield pellets, B, to facilitate handling and solvent recovery. The pellets are passed to a reactor, 3, which is an externally heated rotary kiln, or a fluidised bed, for example operating at 4000C. The solvent is evaporated and is taken off as stream C, then condensed for re-use. The solvent-free pellets, as stream D, are then passed to a second reactor, 4, in which residual carbonaceous matter is burnt off and ash produced as stream E, which forms filter aid for the coal extraction process.The second reactor is preferably maintained atatemperature not exceeding 950"C, and an internallyfiredfurnace, recirculating airfurnace,fluidised bed or other conventional furnace is indicated. Conventional methods of temperature control are expected to be sufficient. The waste heat from the second reactor, indicated by E, is preferably used to heat the first reactor.
Example 3
A coal extract was prepared by digesting a high volatile, weakly caking bituminous coal (from Annesley colliery, near Nottingham, England) CRC 702 in the National Coal Board's Coal Classification: "The Coal
Classification System used by the National Coal Board (Revision of 1964)", National Coal Board Scientific
Control, London, with 4 times its weight of anthracene oil at 420 C for one hour. The product, containing 0.6% mineral matter and 8.8% residual undissolved carbonaceous material, was filtered on a laboratory filter, the filter cake being extruded into pellets and heated to 5000C for 6 minutes in an oven.The pellets were crushed and a fraction less than 425 Fm was tested as a precoat. 10% by weight of the precoat was suspended in anthracene oil and passed through the laboratory filter which used a 200 us mesh woven wire screen as a filter medium, until a layer 0.891lem thick of precoat was formed.
An identical coal extract to that described above was passed through the filter at a temperature of 1 500C and under 1.38 x 105pa (20 psi) pressure. Under steady state conditions, the filtrate contained less than 0.1% mineral matter, which would be acceptable on a commercial scale coal extraction plant.
Under the same experimental conditions, a precoat of "Celite" 560 containing 60% of particles > 1001lem, also produced a filtrate containing less than 0.1% residual mineral matter. Without a precoat, the residual solids in the coat extract were unable to bridge the apertures in the filter screen and no solids removal took place.
Claims (15)
1. A method of filtering coal extract resulting from the extraction of coal with a liquid solvent using a filter aid which is the product of high temperature processing of coal or an ash-rich coal-derived residue under conditions at which the ash component of the coal or residue does not fuse.
2. A method according to claim 1, wherein the residue is filter cake from the filtration of coal extract.
3. A method according to claim 2, wherein, when the filter cake is processed, any solvent present is evaporated and collected for reuse in the extraction of coal.
4. A method according to claim 2 or 3, wherein the filter cake is extruded or otherwise pelletised before the high temperature processing.
5. A method according to any one of the preceding claims, including the step of sizing the product of high temperature processing to an effective particle size for a filter aid.
6. A method according to claim 2,3 or 4, wherein the filter cake is heat treated at a temperature of approximately 600"C for a period of 6 to 30 minutes to substantially remove volatiles and any liquid solvent present.
7. A method according to any one of claims 1 to 5, wherein the high temperature processing of the coal or residue is under combustion conditions at which the ash component of the coal or residue does not fuse.
8. A method according to claim 7 wherein the product of the high temperature processing under combustion conditions is used as a body aid at a concentration of 0.5 to 2% by weight.
9. A method according to claim 8, wherein the product is used as a body aid at a concentration of approximately 1% by weight.
10. A method according to any one of claims 1 to 6, wherein the product of the high temperature processing is used as a precoat filter aid at a concentration of 5 to 20% by weight.
11. A method according to claim 10, wherein the precoat filter aid is used at a concentration of approximately 10% by weight.
12. A method according to claim 1, substantially as hereinbefore described in any one of the Examples.
13. A method of extracting coal, comprising digesting coal in a liquid solvent oil and filtering the undissolved coal and mineral matter from the extract, wherein filter cake from the filtration steps is heat treated under conditions at which the mineral matter does not fuse and the product is sized to an effective filter aid particle size, the product being used as a filter aid in the next cycle of filter operation.
14. A method according to claim 13, substantially as hereinbefore described.
15. A coal extract, whenever prepared by a method according to any one of the preceding claims.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB7932281A GB2035365B (en) | 1978-10-03 | 1979-09-18 | Filtration |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB7839100 | 1978-10-03 | ||
| GB7932281A GB2035365B (en) | 1978-10-03 | 1979-09-18 | Filtration |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| GB2035365A true GB2035365A (en) | 1980-06-18 |
| GB2035365B GB2035365B (en) | 1982-12-01 |
Family
ID=26269055
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB7932281A Expired GB2035365B (en) | 1978-10-03 | 1979-09-18 | Filtration |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB2035365B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3005246A1 (en) * | 1980-02-13 | 1981-08-20 | Bergwerksverband Gmbh, 4300 Essen | METHOD FOR PRODUCING A FILTER AUXILIARY |
-
1979
- 1979-09-18 GB GB7932281A patent/GB2035365B/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3005246A1 (en) * | 1980-02-13 | 1981-08-20 | Bergwerksverband Gmbh, 4300 Essen | METHOD FOR PRODUCING A FILTER AUXILIARY |
| EP0034305A3 (en) * | 1980-02-13 | 1981-12-23 | Bergwerksverband Gmbh | Process for working-up and recycling filtration residues |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2035365B (en) | 1982-12-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 746 | Register noted 'licences of right' (sect. 46/1977) |
Effective date: 19940705 |
|
| 732E | Amendments to the register in respect of changes of name or changes affecting rights (sect. 32/1977) | ||
| PE20 | Patent expired after termination of 20 years |
Effective date: 19990917 |