EP0462953A1 - Verfahren zur Herstellung von Papier - Google Patents
Verfahren zur Herstellung von Papier Download PDFInfo
- Publication number
- EP0462953A1 EP0462953A1 EP91850148A EP91850148A EP0462953A1 EP 0462953 A1 EP0462953 A1 EP 0462953A1 EP 91850148 A EP91850148 A EP 91850148A EP 91850148 A EP91850148 A EP 91850148A EP 0462953 A1 EP0462953 A1 EP 0462953A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- resin
- wet strength
- stock
- paper
- polyamideamine
- 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
- 238000000034 method Methods 0.000 title claims abstract description 22
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 15
- 229920005989 resin Polymers 0.000 claims abstract description 50
- 239000011347 resin Substances 0.000 claims abstract description 50
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 10
- 238000001035 drying Methods 0.000 claims abstract description 9
- 239000000123 paper Substances 0.000 claims description 20
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical group ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 7
- 239000008346 aqueous phase Substances 0.000 claims description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 3
- 239000001913 cellulose Substances 0.000 claims description 3
- 229920002678 cellulose Polymers 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 2
- 239000011087 paperboard Substances 0.000 claims description 2
- 235000011149 sulphuric acid Nutrition 0.000 claims 1
- 239000001117 sulphuric acid Substances 0.000 claims 1
- 229920000768 polyamine Polymers 0.000 abstract description 12
- 230000014759 maintenance of location Effects 0.000 abstract description 10
- 238000010979 pH adjustment Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- QEZDCTNHTRSNMD-UHFFFAOYSA-N 1,2-dichloropropan-2-ol Chemical compound CC(O)(Cl)CCl QEZDCTNHTRSNMD-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- 239000004890 Hydrophobing Agent Substances 0.000 description 1
- JSKQRADCWGNYQD-UHFFFAOYSA-N N.O.[Na] Chemical compound N.O.[Na] JSKQRADCWGNYQD-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- -1 aliphatic dicarboxylic acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 230000003113 alkalizing effect Effects 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- GSTANBWEAXRNHP-UHFFFAOYSA-N azanium;hydrogen carbonate;sodium Chemical compound [NH4+].[Na].OC([O-])=O GSTANBWEAXRNHP-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- KMBPCQSCMCEPMU-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-methylpropane-1,3-diamine Chemical compound NCCCN(C)CCCN KMBPCQSCMCEPMU-UHFFFAOYSA-N 0.000 description 1
- 150000002896 organic halogen compounds Chemical class 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 229940083608 sodium hydroxide Drugs 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
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
- D21H17/55—Polyamides; Polyaminoamides; Polyester-amides
-
- 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
- D21H23/00—Processes or apparatus for adding material to the pulp or to the paper
- D21H23/02—Processes or apparatus for adding material to the pulp or to the paper characterised by the manner in which substances are added
- D21H23/04—Addition to the pulp; After-treatment of added substances in the pulp
- D21H23/06—Controlling the addition
- D21H23/14—Controlling the addition by selecting point of addition or time of contact between components
Definitions
- the present invention relates to a process for the production of paper with wet strength properties using polyamine or polyamideamine based wet strength resins. More particularly the invention relates to a process wherein the wet strength resin is added to the stock at a low pH and wherein the pH of the wet web is increased before the drying.
- Polyamine resins and polyamideamine resins which also are called polyamide polyamine resins or polyamine polyamide resins, are well known additives in papermaking for the production of wet strength paper.
- These cationic thermosetting resins are modified with cross-linking agents such as epihalohydrins, primarily epichlorohydrin, diisocyanates and dichloro isopropanol.
- the main use of these resins is for the production of soft crêpe paper, since they do not impair softness or absorption capability.
- the with cross-linking agents modified polyamine and polyamideamine resins are normally used as additives to the stock at neutral or alkaline pH, usually within the range of from 6 to 11 and most often at a pH of from 6 to 8, since it is considered that this gives the best effect.
- the effect when using polyamine and polyamideamine resins, modified with cross-linking agents such as eg epichlorohydrin, can be considerably improved if the resins are added to the stock at an acid pH whereafter the pH, in a later stage of the paper production, before the drying, is increased for curing of the resin.
- the retention of the resin to the fibres is substantially improved.
- a higher wet strength can be obtained than that previously obtained when the resins were used at a neutral or alkaline stock-pH.
- the process of the invention also makes it possible to decrease the amount of modified resin required to obtain a certain degree of wet strength. Both this possibility and the increased retention are of considerable importance with regard to the environmental impact by resins with halogenated cross-linking agents, such as epichlorohydrin, since the outlet in the waste water of halogenated organic compounds can be decreased.
- the present invention thus relates to a method for the production of paper, board and paperboard, ie cellulose based products in web or sheet form, as defined in the patent claims.
- the polyamine and polyamideamine resins modified with cross-linking agents are per se well known wet strength resins at paper production. Any such resin can be used.
- the present invention relates particularly to the production of paper using modified polyamideamine resin.
- the polyamideamine resins modified with cross-linking agents which can be used in the present process are cationic, water soluble and thermosetting. These types of resins are based on reaction products of cross-linking agents and polyamineamide originating from aliphatic dicarboxylic acids or derivatives of these, such as esters, and polyalkylene polyamines such as diethylenetriamine, tetraethylenepentamine, methylbisaminopropylamine etc..
- polyamideamine resins are such which are modified with epihalohydrins and particularly with epichlorohydrin.
- the polyamideamine resin is added to the stock at a pH of not higher than 6.5 and suitably at a pH of not higher than 5.
- the lower limit for the pH is suitably 4 and it is especially preferred that the pH is within the range of from 4 to 5.
- the pH in the stock supplied to the paper machine can vary within the range of from 3 to 11.
- Required adjustment of the pH in the stock to the paper machine can suitably be made in the machine box.
- the pH adjustment for a more acid pH can be carried out with alum but, in order to increase the possibility to reach a z-potential of 0 in the stock as far as possible, it is preferred to make the pH adjustment with sulfuric acid.
- the modified polyamine or polyamideamine resin can be added to the stock in the machine box or at a suitable point between this and the wire and it is suitably added to the stock in the form of a diluted aqueous solution of 1 to 2%, as conventionally.
- the wet strength resins are usually used in amounts of from about 0.2 to about 3 per cent by weight, calculated as dry on the dry content of the stock, fibers and optional fillers. With the present process, which gives increased retention, the amounts can be considerably reduced, if so desired.
- good effect can be obtained with from 0.1 per cent by weight of the polyamine or polyamideamine resin, calculated as dry on the dry substance of the stock.
- the upper limit is not critical for the wet strength effect and amounts up to about 3 per cent by weight can be used. For reasons of economy, and in order to make use of the advantages with regard to environment which are offered, it is suitable to use amounts up to 2.0 per cent by weight. It is particularly suitable to use amounts within the range of from 0.2 to 1.0 per cent.
- the pH is then to be adjusted to an alkaline pH for curing of the resin.
- This adjustment of pH is made in the wet web formed on the wire, before the drying.
- the stock supplied to and dewatered on the wire usually has a dry substance content of from 0.1 to 0.5 per cent by weight.
- the wet web at the end of the wire has a dry content of from about 15 to about 20 per cent by weight. After the press section of the paper machine the wet web has a dry content of about 25 to about 35 per cent by weight.
- the pH adjustment according to the present invention is made to the wet web before the drying, ie when the web has a dry content of from about 15 to about 35 per cent by weight.
- the pH adjustment of the wet web is suitably made in connection with rolls or other equipment at the final end of the wire, for example at dandy rolls or via press felts.
- rolls or other equipment at the final end of the wire, for example at dandy rolls or via press felts.
- a spray equipment in direct connection to this cylinder by means of which chemicals such as picking chemicals and softeners are added. At such machines it is suitable to carry out pH adjustment by spraying at this dosage point.
- the pH is to be adjusted so that the aqueous phase of the wet web gets a value of not lower than 7.
- the pH adjustment is suitably carried out to a pH not lower than 8.
- the upper limit for the pH is suitably at 10 and it is particularly preferred that the pH is within the range of from 8 to 10.
- the pH adjustment in the wet web is carried out using a suitable alkalizing solution.
- the pH can be adjusted with for example hydroxide or bicarbonate and then particularly sodium- and ammonium hydroxide and sodium- and ammonium bicarbonate respectively. Further, it is, of course, suitable to work with alkaline solutions of fairly high concentration in order to avoid adding too much water which then has to be dried off. However, so strong solutions that discolouring of the cellulose occurs are of course to be avoided.
- the present process gives advantages with regard to retention and level of wet strength. It has also been found that a certain increase of the rate of curing is obtained which means that storage times can be shortened.
- the present process can be used for the production of wet strength paper of different types where modified polyamine or polyamideamine resins are used, and particularly for the production of soft crêpe paper such as tissue for household and sanitary purposes since softness and absorption properties are maintained.
- other paper chemicals such as hydrophobing agents and retention agents can be used.
- Paper having a grammage of 70 g/m2 was produced on an experimental papermaking machine from bleached sulphate pulp beaten to 24°SR.
- a wet strength resin of polyamideamine type modified with epichlorohydrin was used as the sole additive. The resin was added in an amount of 0.4 per cent by weight based on dry pulp.
- the wet strength resin was added to a stock having a pH of 6 to 7 and no subsequent pH adjustment was made.
- test 1b) according to the invention, the wet strength resin was added to a stock having a pH of 4 to 5. The pH in the web formed on the wire was then raised to between 7 and 7.4 before pressing and drying by making the cleaning water to the dandy roll alkaline.
- the wet strength, in km breaking length, of the paper produced in the tests was measured according to SCAN P 38-80.
- the wet strength was measured both after storage for two days and nights at room temperature and after this storage and further curing at 105°C for 1 hour and 2 hours respectively.
- the following tests were carried out on a larger experimental papermaking machine, with a capacity of 0.5 tons per hour, for the production of tissue.
- the machine had an open white water system and a spray box before the drying cylinder.
- the pulp was bleached sulphate beaten to 23° SR.
- the wet strength resin which was used was an epichlorohydrin modified polyamideamine resin which was added in an amount of 1.1 per cent by weight, based on dry pulp. As z-potential regulator towards zero, anionic carboxymethyl cellulose was used. In the tests wherein the pH of the wet web was adjusted this was carried out by spraying with bicarbonate solution.
- the wet strength of the produced tissue paper, in %, was measured according to SCAN P 58-86. The retention of added wet strength resin was also measured.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Paper (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT91850148T ATE95862T1 (de) | 1990-06-20 | 1991-05-30 | Verfahren zur herstellung von papier. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE9002204A SE500454C2 (sv) | 1990-06-20 | 1990-06-20 | Sätt för framställning av våtstarkt papper |
| SE9002204 | 1990-06-20 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0462953A1 true EP0462953A1 (de) | 1991-12-27 |
| EP0462953B1 EP0462953B1 (de) | 1993-10-13 |
Family
ID=20379829
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP91850148A Expired - Lifetime EP0462953B1 (de) | 1990-06-20 | 1991-05-30 | Verfahren zur Herstellung von Papier |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP0462953B1 (de) |
| AT (1) | ATE95862T1 (de) |
| DE (1) | DE69100499T2 (de) |
| SE (1) | SE500454C2 (de) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6740373B1 (en) | 1997-02-26 | 2004-05-25 | Fort James Corporation | Coated paperboards and paperboard containers having improved tactile and bulk insulation properties |
| US6919111B2 (en) | 1997-02-26 | 2005-07-19 | Fort James Corporation | Coated paperboards and paperboard containers having improved tactile and bulk insulation properties |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2401267A1 (fr) * | 1977-08-26 | 1979-03-23 | Ciba Geigy Ag | Procede de preparation de papier ou carton encolle a partir de polyelectrolytes et de produits d'addition epoxyde-amine-polyamide |
-
1990
- 1990-06-20 SE SE9002204A patent/SE500454C2/sv unknown
-
1991
- 1991-05-30 AT AT91850148T patent/ATE95862T1/de not_active IP Right Cessation
- 1991-05-30 DE DE91850148T patent/DE69100499T2/de not_active Expired - Fee Related
- 1991-05-30 EP EP91850148A patent/EP0462953B1/de not_active Expired - Lifetime
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2401267A1 (fr) * | 1977-08-26 | 1979-03-23 | Ciba Geigy Ag | Procede de preparation de papier ou carton encolle a partir de polyelectrolytes et de produits d'addition epoxyde-amine-polyamide |
Also Published As
| Publication number | Publication date |
|---|---|
| DE69100499D1 (de) | 1993-11-18 |
| EP0462953B1 (de) | 1993-10-13 |
| DE69100499T2 (de) | 1994-02-03 |
| SE9002204L (sv) | 1991-12-21 |
| SE9002204D0 (sv) | 1990-06-20 |
| ATE95862T1 (de) | 1993-10-15 |
| SE500454C2 (sv) | 1994-06-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US6228217B1 (en) | Strength of paper made from pulp containing surface active, carboxyl compounds | |
| US4964954A (en) | Process for the production of paper | |
| EP0335575B2 (de) | Herstellung von Papier und Pappe | |
| US4722964A (en) | Epoxidized polyalkyleneamine-amide wet strength resin | |
| EP1309758B1 (de) | Verfahren zur papierherstellung | |
| US6918995B2 (en) | Process for the production of paper | |
| US5225047A (en) | Crosslinked cellulose products and method for their preparation | |
| EP0348366B2 (de) | Verfahren zur Papierherstellung | |
| US3640841A (en) | Method for controlling adhesion of paper on yankee drier with polyamides and resultant products | |
| KR0159921B1 (ko) | 양이온성 및 음이온성 중합체의 혼합물, 그 제법 및 종이용 건조강도 개선 첨가제로서의 용도 | |
| CA2159593C (en) | Process of making paper | |
| US4191610A (en) | Upgrading waste paper by treatment with sulfite waste liquor | |
| FI83443C (fi) | Anvaendning av karboxylsyraestrar och/ eller polyetrar vid pappersframstaellning. | |
| US7029553B1 (en) | Urea sulfate and urea hydrochloride in paper and pulp processing | |
| EP0462953B1 (de) | Verfahren zur Herstellung von Papier | |
| US6372088B1 (en) | Enhancer performance for PEO | |
| US4372815A (en) | Method for upgrading paper and the product formed thereby | |
| FI68435B (fi) | Lignocellulosamaterial med foerbaettrad styrka avvattningsfoermaoga och malbarhet samt saett att framstaella detta | |
| CA1101158A (en) | Strengthening agents | |
| EP0722011B1 (de) | Verfahren zur Herstellung von Tissuepapier, Zeitungsdruckpapier, Papier oder Karton | |
| US3298902A (en) | Process of forming cellulosic paper containing tris-(1-aziridinyl) phosphine oxide and polyethylene imine and paper thereof | |
| JP4802015B2 (ja) | 外添型ピッチコントロール剤 | |
| US1808073A (en) | Method of improving paper machine operation | |
| ZA200301792B (en) | A process for the production of paper. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH DE DK ES FR GB GR IT LI NL SE |
|
| 17P | Request for examination filed |
Effective date: 19920410 |
|
| 17Q | First examination report despatched |
Effective date: 19920708 |
|
| GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
| AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE CH DE DK ES FR GB GR IT LI NL SE |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRE;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.SCRIBED TIME-LIMIT Effective date: 19931013 Ref country code: AT Effective date: 19931013 Ref country code: LI Effective date: 19931013 Ref country code: ES Free format text: THE PATENT HAS BEEN ANNULLED BY A DECISION OF A NATIONAL AUTHORITY Effective date: 19931013 Ref country code: DK Effective date: 19931013 Ref country code: CH Effective date: 19931013 Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 19931013 |
|
| REF | Corresponds to: |
Ref document number: 95862 Country of ref document: AT Date of ref document: 19931015 Kind code of ref document: T |
|
| REF | Corresponds to: |
Ref document number: 69100499 Country of ref document: DE Date of ref document: 19931118 |
|
| ET | Fr: translation filed | ||
| REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
| PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
| 26N | No opposition filed | ||
| EAL | Se: european patent in force in sweden |
Ref document number: 91850148.7 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 20010417 Year of fee payment: 11 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20010518 Year of fee payment: 11 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20010522 Year of fee payment: 11 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20010530 Year of fee payment: 11 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 20010531 Year of fee payment: 11 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 20010717 Year of fee payment: 11 |
|
| REG | Reference to a national code |
Ref country code: FR Ref legal event code: CD |
|
| REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020530 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020531 Ref country code: SE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020531 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20021201 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20021203 |
|
| EUG | Se: european patent has lapsed | ||
| GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20020530 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20030131 |
|
| NLV4 | Nl: lapsed or anulled due to non-payment of the annual fee |
Effective date: 20021201 |
|
| REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |