NZ230427A - Process for dewatering cellulose pulp on a wire - Google Patents
Process for dewatering cellulose pulp on a wireInfo
- Publication number
- NZ230427A NZ230427A NZ230427A NZ23042789A NZ230427A NZ 230427 A NZ230427 A NZ 230427A NZ 230427 A NZ230427 A NZ 230427A NZ 23042789 A NZ23042789 A NZ 23042789A NZ 230427 A NZ230427 A NZ 230427A
- Authority
- NZ
- New Zealand
- Prior art keywords
- colloid
- process according
- anionic
- cationic
- aluminate
- Prior art date
Links
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/54—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/41—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
- D21H17/44—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups cationic
- D21H17/45—Nitrogen-containing groups
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/63—Inorganic compounds
- D21H17/67—Water-insoluble compounds, e.g. fillers, pigments
- D21H17/68—Water-insoluble compounds, e.g. fillers, pigments siliceous, e.g. clays
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dispersion Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Paper (AREA)
- Making Paper Articles (AREA)
- Diaphragms For Electromechanical Transducers (AREA)
- Polarising Elements (AREA)
- Electronic Switches (AREA)
Abstract
A method for the production of paper by forming and dewatering a suspension of cellulose containing fibres on a wire. The forming and dewatering takes place in the presence of an anionic, inorganic colloid, an aluminate and a cationic synthetic polymer. The process gives improved dewatering and improved retention of fines and optional fillers.
Description
New Zealand Paient Spedficaiion for Paient Number £30427
230 4 27!
NO DRAWINGS
, -T< «•
Priority Date(s):
Complete Specification Filed: •.?: A*?. Qhs: ?£«£&/&>.>lit,• • • -
Publication Date:
£? JUN 691
P.O." Journal. No: J
\b*b
N.Z. No.
NEW ZEALAND Patents Act 1953 COMPLETE SPECIFICATION A PROCESS FOR THE PRODUCTION OF PAPER
We, EKA NOBEL AB, a Swedish company, of S-445 01 Surte, Sweden do hereby declare the invention, for which we pray that a patent nay be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement
(Followed by 1A)
230 427'
lA
A process for the production of paper The present invention relates to a process for the production of paper utilizing an improved retention- and dewatering system. More particularly the invention relates to the use of a combination of a cationic synthetic polymer, an anionic inorganic colloid and aluminate as retention- and dewatering system in papermaking.
It is previously known to use combinations of cat-ionic retention agents and inorganic colloids as retention-and dewatering agents in the production of paper. The European patent application 0218674 discloses the use of polyacrylamide in combination with anionic silica sols as binders and retention agents. It is assumed that the colloidal particles of the sols with their strong charges produce a cross-linking of the polymeric retention agents and that very good retention and dewatering effect is obtained through this. From the British patent 2015614 it is further known to use polymeric cationic retention agents in combination with poly alum i num compounds. It is further known from the US patent 4,643,801 to use a combination of a cationic starch, an anionic silica sol and an anionic high molecular weight polymer, particularly an anionic polyacrylamide, as a binder in papermaking. The three component system according to the US patent can be used with additional aluminum compounds, such as alum, sodium aluminate or polyhydroxyaluminum chloride.
According to the present invention it has been found that the retention- and dewatering effect in papermaking is improved if an aluminate is used in combination with cationic, synthetic polymer and an anionic inorganic colloid. As the dewatering effect is increased the speed of the papermachine can be increased and, further, less water will have to be dried off in the drying section of the paper machine.
The present invention thus . relates to a process for the production of paper by forming and dewatering a suspension of cellulose containing fibres, and optionally fillers, on a wire whereby the forming and dewatering takes
m
. ■ 25QA77
2
place in the presence of em anionic inorganic colloid
AYfinHing polymeric silicic acid with, a specific surface area of at least 1050 nfVg, an aluminate and a cationic synthetic polymer.
The three components can be added to the fibre stock in arbitrary order. The best effect is obtained if the 5 aluminate is added to the stock first, followed by addition v of cationic synthetic polymer and then the anionic inor ganic colloid. A considerable improvement, in comparison with known technique, is obtained also when the anionic inorganic colloid is first added to the stock and the 10 cationic polymer and the aluminate are added subsequently, in any order. Separate addition of the three respective components is preferred although it is possible to pre-mix two of the components before the addition.
As cationic synthetic polymers for use according to 15 the present invention such cationic, organic nitrogen containing polymers which are conventionally used as retention agents and/or wet strength agents in papermaking are suitable. Particularly suitable are cationic polyacryl-amides, polyethyleneimines, poly ami ne resins and polyamido-20 amine resins etc. Polyamine resins and polyamidoamine resins are suitably used in their epichl orohydrine modified form. Other cationic synthetic polymers which can also be used are the cationic melamine-formaldehyde and urea— formaldehyde wet strength resins. The amount of the cat-25 ionic synthetic polymer should suitably be within the range of from 0.01 to 3 per cent by weight, preferably within the range of from 0.03 to 2 per cent by weight, based on dry fibres and optional fillers.
/ " The anionic inorganic colloids which are used are
• per se previously known for use in papermaking. As examples of such colloids can be mentioned montmorillonite, ben— tonite, titanyl sulphate sols, silica sols, aluminum modified silica sols or aiiim-inum silicate sols. The terms colloid anfl colloidal indicate very smal 1 particles. The 35 particles of the anionic substances should suitably have a specific surface area above 50 m2/g, more suitably above 100 m2/g, preferably within the range of 50 to 1000
m2/g. Silica based collwidj ul u Qii^flgeretred anionic inor-
r PAT^*-1' —
17 MAY 19-1 |
' —1
230427
3
gaiiic colloid.
Particularly suitable silica based colloids are the silica sols with, colloidal particles as disclosed in the European patent 41056, which is hereby incorporated by reference in this application, and the aluminum containing silica sols which are disclosed in the European patent application 0218674, which likewise is incorporated by reference. The colloidal silica in the sols should preferably have a specific surface area of 50 to 1000 m2/g and more preferably of about 100 to 1000 m2/g, and the best results have been obtained when the specific surface area has been about 300 to 700 m2/g. It has been found that the colloidal silica particles should suitably have a particle size below 20 nm and preferably from about 10 down to about
1 nm (a colloidal silica particle having a specific surface area of about 550 m2/g corresponds to an average particle size of about 5 nm). Good results are obtained with the mentioned silica sols in the form of an alkali stabilized sol which contains about 2 to 60 per cent by weight of SiC>2, preferably from about 4 to 30 per cent by weight of S102. The silica sol can be stabilized with alkali in a molar ratio of Si02:M20 of from 10:1 to 300:1, preferably 15:1 to 100:1 (M is an ion from the group Na, K, Li and NH4). As mentioned above good results are obtained using colloidal particles which have at least a surface layer of aluminum silicate or aluminum modified silica sol, so that' the surface groups of the particles contain silicon and aluminum atoms in a ratio of from 9.5:0.5 to 7.5:2.5 and the given surfaces and particle sizes also apply to these sols. Silica sols which fulfil the above given specific- . ations sure available commercially, eg from Eka Nobel AB.
The amount of anionic colloid which is added to the stock should suitably be within the range of from 0.005 to
2 per cent by weight, preferably from 0.01 to 0.4 per cent by weight, based on dry cellulose fibres and optional fillers. The concentration of the colloid, preferably colloidal silica, in the sol added to the stock is not • critical. Prom a practical point of view it is suitable
230427
©
o
©
4
that the sols at the addition to the stock have a concentration of from 0.05 to 5.0 per cent by weight.
Aluminate refers to alkali aluminate which per se is well-known for use in paper production, particularly for 5 hydrophobing with rosin. Sodium aluminate (Na2Al204) is preferably used, but potassium aluminate can of course also be used even if is less advantageous from an economical point of view. The amount of aluminate can vary within wide limits. The addition of aluminate to the stock is suitably 10 made in the form of aqueous solutions and the concentration in the solutions is not critical but is adjusted with regard to practical considerations. According to the invention it has been found that already very <=amal i amounts of aluminate, with regard to the amount of anionic inor-15 ganic colloid, give considerable improvements in the dewatering effect. An improvement is obtained already at a weight ratio aluminate, calculated as AI2O3, to inorganic colloid of 0.01:1. The upper limit is not critical. However, no improvements worth mentioning are obtained when 20 the ratio of aluminate to inorganic colloid exceeds 3:1. The ratio is suitably within the range of from 0.02:1 to 1.5:1 and preferably from 0.05:1 to 0.7:1. The given ratios all relate to weight ratio between aluminate, calculated as AI2O3, and the inorganic colloid.
The improved retention- and dewatering effect with the system of the invention is obtained over a broad pH range for the stock. The pH can be within the range from about 4 to about 10. The pH is suitably above 5 and preferably within the range of from 6 to 9. If the desired pH is 30 not reached by the addition of the aluminate solution, which in itself is alkaline, the pH of the stock can be adjusted for example by addition of sodium hydroxide. If alkaline buffering fillers are used, for example chalk, a suitable pH is normally reached without adjustments. Other 35 fillers than chalk can of course also be used, but then care has to be taken so that the pH of the stock is kept within the above given limits.
At paper production according to the invention
230427
mineral fillers of conventional types can be used, for example kaolin, titanium dioxide, gypsum, chalk and talcum. The term "mineral filler" is herein used to include, in addition to these fillers, also wollastonite and glass fibres and also mineral low density fillers, such as expanded perlite. The mineral filler is usually added in the form of an aqueous slurry in conventional concentrations used for such fillers. The filler can optionally be treated before the addition to the stock with components of the dewatering- and retention- system of the invention, for example by treatment with the cationic synthetic polymer and the aluminate or the inorganic colloid, whereafter the remaining component is added to the stock.
The three-component system of the invention can be used at production of paper from different types of stocks of cellulose containing fibres. The stocks should suitably contain at least 50 per cent by weight of cellulose containing fibres. The three-component system can for example be used for stocks of fibres from chemical pulp, such as sulphate and sulphite pulp, thermomechanical pulp, refiner pulp and groundwood pulp from as well hardwood as softwood. It can of course also be used for stocks from recycled fibres. The terms paper and papermaking, which are used herein do of course not only include paper and its production, but also other cellulose fibre containing sheet or web form products, such as pulp sheet, board and cardboard and their production.
The process according the invention can be carried out in per se known manner and with other additions to the fibre stock, such as sizing agents etc.
The invention is further illustrated in the following examples wherein parts and per cent relate to parts by weight and per cent by weight Tin!ess otherwise stated.
Example 1
In the following tests the dewatering effect was investigated by means of a "Canadian Freeness Tester", which is the usual method for characterizing the dewatering capability according to SCAN-C 21:65.
230427
6
The stock was based on bleached birch/pine sulphate pulp (60:40) and contained 30 per cent by weight of chalk. The pH of the stock was 8.5 and CSF was 300 ml.
In the table amounts for the chemical additions refer to ton dry stock system (fibres+fillers). The anionic colloid was an alkali stabilized silica sol with a specific surface area of 500 m2/g. The cationic synthetic polymer was a cationic polyacrylamide of medium cationicity sold by Allied Colloids under the name Percol 292. The sodium a Tumi nate was added in the form of a 0.025% aqueous solution and the given amounts of aluminate are expressed as kg AI2O3. The additions of chemicals were made to l 1 diluted stock (about 0.3%) with intervals of 15 seconds under agitation in the order aluminate, cationic polymer, inorganic colloid. The flocked stock was transferred to the freeness apparatus and measurements were made 15 seconds after the last addition. The water which is collected is a measurement of the dewatering effect and is expressed in ml Canadian Standard Freeness (CSF). The water obtained in the tests using the three components was very clear and this shows that a good retention of the fines material to the flocks had also been obtained.
Test
AI2O3
Cationic
Anionic
CSF
No.
kq/t polymer kq/t
Colloid kq/t ml
1
-
-
—
300
2
-
0.3
-
370
3
-
0.6
-
385
4
-
0.9 .
-
390
0.15
-
—
290"
6
0.15
0.3
—
350
7
-
-
1.0
295
8
0.15
—
1.0
290
9
-
0.3
0.5
420
-
0.3
1.0
430
11
-
0.3
1.5
440
12
0.075
0.3
0.5
495
13
0.15
0.3
1.0
520
14
0.225
0.3
1.5
515
o
2304 2
Test AI2O3 Cationic Anionic CSF
No. kq/t polymer kq/t Colloid kq/t ml
- 0.6 0.5 425
16 - 0.6 1.0 490 5 17 - 0.6 1.5 510
C18 0.075 0.6 0.5 495
19 0.15 0.6 1.0 570
0.225 0.6 1.5 585 As evident also use of very small amounts of alumi-
nate gives a considerably improved dewatering effect for the system of cationic polymer and anionic colloid. The corresponding effect of the aluminate is not obtained if it is used in combination with only cationic polymer or only anionic colloid.
Example 2
This example corresponded entirely to example 1 with the only difference that other cationic synthetic polymers were used. These were A) an epichlorohydrine modified polyamidoamine resin sold by Hercules Inc. under the name 20 Kymene 557 H and B) a modified polyamine resin sold by Hercules Inc. under the name Delfloc-50.
0
Test
AI2O3
Cat.
Polymer
Anionic CSF
No.
kq/t type;kq/t
Colloid kq/t ml
1
-
-
300
2
-
A;
0.6
305
3
-
A;
1.2
315
4
-
A;
2.4
315
-
A;
1.2
0.5 325
6
-
A;
1.2
1.0 330
7
-
A;
1.2
1.5 310
8
0.075
A;
1.2
0.5 360
9
0.15
A;
1.2
1.0 390
0.225
A;
1.2
1.5 410
11
0.30
A;
1.2
2.0 395
12
-
B;
1.2
290
13
-
B;
1.2
1.5 280
14
0.225
B;
1.2
1.5 335
2304
Example 3
In this example a groundwood stock was used which did not contain any fillers. To the stock 0.5 g/1 of Na2S04 • IOH2O had been added to give an ion strength 5 corresponding to the one under large scale conditions. The cationic polymer was the same polyacrylamide as in Example 1. The anionic colloid was an aluminum modified, 15% alkali stabilized, silica sol where the surface of the colloidal particles had been modified with 9% aluminum atoms and the 10 surface area of the particles was 500 m2/g. The order of addition was sodium aluminate, cationic polymer followed by anionic colloid. Tests were made both with a stock pH of 6 and a stock pH of 7.5 whereby the pH had been adjusted with diluted H2SO4 and diluted NaOH respectively.
Test
AI2O3
Cationic
Anionic
CSF
NO
kq/t polymer kq/t colloid kq/t ml
PH 6.0
1
-
-
-
120
2
-
0.3
-
190
3
-
0.6
-
220
4
—
0.9
1.2
-
250
6
-
0.6
0.5
275
7
-
0.6
1.0
305
8
-
0.6
•
r-4
300
9
0.075
0.6
0.5
325
0.15
0.6
1.0
345
11
0.225
0.6
1.5
350
PH 7.5
12
-
0.6
-
220
13
-
0.6
0.5
245
14
-
0.6
1.0
270
-
0.6
1.5
275
16
0.075
0.6
0.5
295
17
0.15
0.6
1.0
325
18
0.225
0.6
1.5
340
19
-
0.9
1.5
310
0.225
0.9
1.5
370
Claims (11)
1. A process for the production of paper by forming apf? dewatering a suspension of cellulose containing fibres on a wire, characterized in that the forming and dewatering 5 takes place in the presence of an anionic inorganic colloid excluding polymeric silicic acid with a specific surface area of at least 1050m2/g, an aluminate and a cationic synthetic polymer.
2. A process according to claim 1, characterized in that the anionic colloid is a silica based colloid.
3. A process according to claim 1 or 2, characterized 10 in that the colloid is a silica sol, a silica sol with particles having at least a surface layer of aluminum silicate or an aluminum modified silica sol.
4. A process accord g to claim 1, 2 or 3, characterized in that the particles of the colloid have a speci- 15 fic surface area within the range of from 50 to 1000 m2/g.
5. A process according to claim 3, characterized in that the particle size of the colloid is 20 nm at the most.
6. A process according to claim 1, characterized in that the cationic synthetic polymer is a cationic poly- 20 acrylamide, polyethyleneimine, polyamine or polyamidoamine.
7. A process according to any of the preceding claims, characterized in that the aluminate is added to the fibre suspension before the anionic inorganic colloid and the cationic synthetic polymer. 25
8. A process according to any of claims 1, 2, 3, 4 or 5, characterized in that the amount of anionic inorganic colloid is within the range of from 0.005 to 2 per cent by weight, based on dry fibres and optioned, fillers.
9. A process according to cl aim 1 or 6, characterized 30 in that the amount of cationic synthetic polymer is within the range of from 0.01 to 3 per cent by weight, based on dry fibres and optional fillers.
10. A process according to claim 1, characterized in that the weight ratio of aluminate, calculated as AL2O3, to 35 anionic inorganic colloid is within the range of from 0.01:1 to 3:1.
11. A process according to claim 1 substantially as herein described or exemplify 1 EKA NOBS
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE8803065A SE467627B (en) | 1988-09-01 | 1988-09-01 | SET ON PAPER MAKING |
Publications (1)
Publication Number | Publication Date |
---|---|
NZ230427A true NZ230427A (en) | 1991-06-25 |
Family
ID=20373187
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NZ230427A NZ230427A (en) | 1988-09-01 | 1989-08-25 | Process for dewatering cellulose pulp on a wire |
Country Status (13)
Country | Link |
---|---|
EP (1) | EP0357574B1 (en) |
JP (1) | JP2521539B2 (en) |
AT (1) | ATE99010T1 (en) |
AU (1) | AU605997B2 (en) |
BR (1) | BR8904283A (en) |
CA (1) | CA1334324C (en) |
DE (1) | DE68911626T2 (en) |
ES (1) | ES2048323T3 (en) |
FI (1) | FI90448C (en) |
NO (1) | NO171567C (en) |
NZ (1) | NZ230427A (en) |
PT (1) | PT91611B (en) |
SE (1) | SE467627B (en) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4795531A (en) * | 1987-09-22 | 1989-01-03 | Nalco Chemical Company | Method for dewatering paper |
US4927498A (en) * | 1988-01-13 | 1990-05-22 | E. I. Du Pont De Nemours And Company | Retention and drainage aid for papermaking |
SE500367C2 (en) * | 1989-11-09 | 1994-06-13 | Eka Nobel Ab | Silica soles and process for making paper |
BR9205973A (en) * | 1991-07-02 | 1994-08-02 | Eka Nobel Ab | Papermaking process |
DE4437118A1 (en) * | 1994-10-05 | 1996-04-11 | Technocell Dekor Gmbh & Co Kg | Base paper for decorative coating systems |
US5846384A (en) * | 1995-06-15 | 1998-12-08 | Eka Chemicals Ab | Process for the production of paper |
SE9502184D0 (en) * | 1995-06-15 | 1995-06-15 | Eka Nobel Ab | A process for the production of paper |
US5595630A (en) * | 1995-08-31 | 1997-01-21 | E. I. Du Pont De Nemours And Company | Process for the manufacture of paper |
SE9504081D0 (en) * | 1995-11-15 | 1995-11-15 | Eka Nobel Ab | A process for the production of paper |
US7169261B2 (en) | 1999-05-04 | 2007-01-30 | Akzo Nobel N.V. | Silica-based sols |
PL201407B1 (en) | 1999-05-04 | 2009-04-30 | Akzo Nobel Nv | Silica-based sols |
US6379501B1 (en) | 1999-12-14 | 2002-04-30 | Hercules Incorporated | Cellulose products and processes for preparing the same |
WO2003083212A1 (en) * | 2002-04-03 | 2003-10-09 | Seiko Pmc Corporation | Method for producing paper and agent for improving yield |
FI121119B (en) † | 2003-04-15 | 2010-07-15 | Kemira Oyj | Procedure for making paper |
JP4168088B2 (en) | 2006-12-28 | 2008-10-22 | 東京金属工業株式会社 | clip |
CN103556532B (en) * | 2013-10-31 | 2016-01-20 | 东莞理文造纸厂有限公司 | A kind of retention aid for paper making and preparation method thereof |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE8403062L (en) * | 1984-06-07 | 1985-12-08 | Eka Ab | PAPER MANUFACTURING PROCEDURES |
SE451739B (en) * | 1985-04-03 | 1987-10-26 | Eka Nobel Ab | PAPER MANUFACTURING PROCEDURE AND PAPER PRODUCT WHICH DRAINAGE AND RETENTION-IMPROVING CHEMICALS USED COTTONIC POLYACRYLAMIDE AND SPECIAL INORGANIC COLLOID |
SE8701252D0 (en) * | 1987-03-03 | 1987-03-25 | Eka Nobel Ab | SET FOR PAPER MAKING |
US4795531A (en) * | 1987-09-22 | 1989-01-03 | Nalco Chemical Company | Method for dewatering paper |
US4927498A (en) * | 1988-01-13 | 1990-05-22 | E. I. Du Pont De Nemours And Company | Retention and drainage aid for papermaking |
SE461156B (en) * | 1988-05-25 | 1990-01-15 | Eka Nobel Ab | SET FOR PREPARATION OF PAPER WHICH SHAPES AND DRAINAGE OWN ROOMS IN THE PRESENCE OF AN ALUMINUM SUBSTANCE, A COTTONIC RETENTION AND POLYMER SILICON ACID |
-
1988
- 1988-09-01 SE SE8803065A patent/SE467627B/en not_active IP Right Cessation
-
1989
- 1989-08-09 EP EP89850252A patent/EP0357574B1/en not_active Expired - Lifetime
- 1989-08-09 ES ES89850252T patent/ES2048323T3/en not_active Expired - Lifetime
- 1989-08-09 AT AT89850252T patent/ATE99010T1/en not_active IP Right Cessation
- 1989-08-09 DE DE89850252T patent/DE68911626T2/en not_active Expired - Lifetime
- 1989-08-25 NZ NZ230427A patent/NZ230427A/en unknown
- 1989-08-25 BR BR898904283A patent/BR8904283A/en not_active IP Right Cessation
- 1989-08-28 CA CA000609515A patent/CA1334324C/en not_active Expired - Lifetime
- 1989-08-28 AU AU40840/89A patent/AU605997B2/en not_active Expired
- 1989-08-29 JP JP1220495A patent/JP2521539B2/en not_active Expired - Lifetime
- 1989-08-30 FI FI894075A patent/FI90448C/en active IP Right Grant
- 1989-08-31 NO NO893500A patent/NO171567C/en not_active IP Right Cessation
- 1989-09-01 PT PT91611A patent/PT91611B/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
EP0357574A3 (en) | 1991-10-23 |
ES2048323T3 (en) | 1994-03-16 |
NO893500D0 (en) | 1989-08-31 |
FI894075A0 (en) | 1989-08-30 |
FI90448B (en) | 1993-10-29 |
BR8904283A (en) | 1990-04-17 |
JPH0299692A (en) | 1990-04-11 |
AU605997B2 (en) | 1991-01-24 |
PT91611B (en) | 1995-05-31 |
EP0357574B1 (en) | 1993-12-22 |
FI894075A (en) | 1990-03-02 |
SE8803065D0 (en) | 1988-09-01 |
NO893500L (en) | 1990-03-02 |
NO171567B (en) | 1992-12-21 |
SE8803065L (en) | 1990-03-02 |
JP2521539B2 (en) | 1996-08-07 |
SE467627B (en) | 1992-08-17 |
DE68911626T2 (en) | 1994-04-07 |
CA1334324C (en) | 1995-02-14 |
AU4084089A (en) | 1990-03-29 |
NO171567C (en) | 1993-03-31 |
EP0357574A2 (en) | 1990-03-07 |
PT91611A (en) | 1990-03-30 |
FI90448C (en) | 1994-02-10 |
ATE99010T1 (en) | 1994-01-15 |
DE68911626D1 (en) | 1994-02-03 |
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