NO301148B1 - Fremgangsmåte for fremstilling av spröytbare blandinger for jordbruksformål og anvendelse av slike blandinger - Google Patents
Fremgangsmåte for fremstilling av spröytbare blandinger for jordbruksformål og anvendelse av slike blandinger Download PDFInfo
- Publication number
- NO301148B1 NO301148B1 NO923732A NO923732A NO301148B1 NO 301148 B1 NO301148 B1 NO 301148B1 NO 923732 A NO923732 A NO 923732A NO 923732 A NO923732 A NO 923732A NO 301148 B1 NO301148 B1 NO 301148B1
- Authority
- NO
- Norway
- Prior art keywords
- polymer
- weight
- active ingredient
- oil
- acrylamide
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 67
- 238000004519 manufacturing process Methods 0.000 title description 2
- 229920000642 polymer Polymers 0.000 claims abstract description 84
- 239000004480 active ingredient Substances 0.000 claims abstract description 47
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims abstract description 33
- 239000005562 Glyphosate Substances 0.000 claims abstract description 31
- 229940097068 glyphosate Drugs 0.000 claims abstract description 31
- 239000006185 dispersion Substances 0.000 claims abstract description 28
- 230000009885 systemic effect Effects 0.000 claims abstract description 17
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 8
- 239000002245 particle Substances 0.000 claims description 44
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 34
- 239000012071 phase Substances 0.000 claims description 27
- 239000000178 monomer Substances 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 21
- 239000007921 spray Substances 0.000 claims description 15
- 239000003995 emulsifying agent Substances 0.000 claims description 14
- 239000000839 emulsion Substances 0.000 claims description 14
- 239000008346 aqueous phase Substances 0.000 claims description 13
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 10
- 125000000129 anionic group Chemical group 0.000 claims description 10
- 125000002091 cationic group Chemical group 0.000 claims description 9
- 239000004009 herbicide Substances 0.000 claims description 8
- 238000002156 mixing Methods 0.000 claims description 7
- 229920002401 polyacrylamide Polymers 0.000 claims description 5
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- 229940047670 sodium acrylate Drugs 0.000 claims description 4
- 239000005556 hormone Substances 0.000 claims description 2
- 229940088597 hormone Drugs 0.000 claims description 2
- 239000005648 plant growth regulator Substances 0.000 claims description 2
- 239000005974 Chlormequat Substances 0.000 claims 1
- 239000005630 Diquat Substances 0.000 claims 1
- JUZXDNPBRPUIOR-UHFFFAOYSA-N chlormequat Chemical compound C[N+](C)(C)CCCl JUZXDNPBRPUIOR-UHFFFAOYSA-N 0.000 claims 1
- SYJFEGQWDCRVNX-UHFFFAOYSA-N diquat Chemical compound C1=CC=[N+]2CC[N+]3=CC=CC=C3C2=C1 SYJFEGQWDCRVNX-UHFFFAOYSA-N 0.000 claims 1
- 230000001976 improved effect Effects 0.000 abstract description 5
- 229920003169 water-soluble polymer Polymers 0.000 abstract description 3
- 241000196324 Embryophyta Species 0.000 description 30
- 239000000243 solution Substances 0.000 description 18
- 230000000694 effects Effects 0.000 description 13
- 230000004913 activation Effects 0.000 description 11
- 239000012141 concentrate Substances 0.000 description 10
- 238000005507 spraying Methods 0.000 description 10
- 230000008901 benefit Effects 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- 238000011282 treatment Methods 0.000 description 7
- 230000000996 additive effect Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 230000006872 improvement Effects 0.000 description 5
- 230000001665 lethal effect Effects 0.000 description 5
- 230000005945 translocation Effects 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 230000001965 increasing effect Effects 0.000 description 4
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 229920000831 ionic polymer Polymers 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000001593 sorbitan monooleate Substances 0.000 description 3
- 229940035049 sorbitan monooleate Drugs 0.000 description 3
- 235000011069 sorbitan monooleate Nutrition 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- OIUCPPFBFOLPIO-UHFFFAOYSA-N tetratriacontyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C(C)=C OIUCPPFBFOLPIO-UHFFFAOYSA-N 0.000 description 3
- 230000032258 transport Effects 0.000 description 3
- IEORSVTYLWZQJQ-UHFFFAOYSA-N 2-(2-nonylphenoxy)ethanol Chemical compound CCCCCCCCCC1=CC=CC=C1OCCO IEORSVTYLWZQJQ-UHFFFAOYSA-N 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 241000183024 Populus tremula Species 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 241001464837 Viridiplantae Species 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 239000004815 dispersion polymer Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000012010 growth Effects 0.000 description 2
- 238000003306 harvesting Methods 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- 229920000847 nonoxynol Polymers 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 230000010019 sublethal effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000009827 uniform distribution Methods 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- WNTGYJSOUMFZEP-SSDOTTSWSA-N (R)-mecoprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-SSDOTTSWSA-N 0.000 description 1
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 1
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 description 1
- ZHCGVAXFRLLEFW-UHFFFAOYSA-N 2-methyl-3-(prop-2-enoylamino)propane-1-sulfonic acid Chemical compound OS(=O)(=O)CC(C)CNC(=O)C=C ZHCGVAXFRLLEFW-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 241000218642 Abies Species 0.000 description 1
- 239000005500 Clopyralid Substances 0.000 description 1
- 235000001543 Corylus americana Nutrition 0.000 description 1
- 240000007582 Corylus avellana Species 0.000 description 1
- 235000007466 Corylus avellana Nutrition 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PQKBPHSEKWERTG-UHFFFAOYSA-N Fenoxaprop ethyl Chemical group C1=CC(OC(C)C(=O)OCC)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 PQKBPHSEKWERTG-UHFFFAOYSA-N 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000005574 MCPA Substances 0.000 description 1
- 239000005576 Mecoprop-P Substances 0.000 description 1
- 239000005584 Metsulfuron-methyl Substances 0.000 description 1
- WGVWLKXZBUVUAM-UHFFFAOYSA-N Pentanochlor Chemical compound CCCC(C)C(=O)NC1=CC=C(C)C(Cl)=C1 WGVWLKXZBUVUAM-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- CSPPKDPQLUUTND-NBVRZTHBSA-N Sethoxydim Chemical compound CCO\N=C(/CCC)C1=C(O)CC(CC(C)SCC)CC1=O CSPPKDPQLUUTND-NBVRZTHBSA-N 0.000 description 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 125000000746 allylic group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229920006318 anionic polymer Polymers 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000002361 compost Substances 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- OSUHJPCHFDQAIT-UHFFFAOYSA-N ethyl 2-{4-[(6-chloroquinoxalin-2-yl)oxy]phenoxy}propanoate Chemical group C1=CC(OC(C)C(=O)OCC)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 OSUHJPCHFDQAIT-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- VAIZTNZGPYBOGF-CYBMUJFWSA-N fluazifop-P-butyl Chemical group C1=CC(O[C@H](C)C(=O)OCCCC)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 VAIZTNZGPYBOGF-CYBMUJFWSA-N 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000007952 growth promoter Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 231100000518 lethal Toxicity 0.000 description 1
- RSMUVYRMZCOLBH-UHFFFAOYSA-N metsulfuron methyl Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=NC(OC)=N1 RSMUVYRMZCOLBH-UHFFFAOYSA-N 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Ultra Sonic Daignosis Equipment (AREA)
- Magnetic Resonance Imaging Apparatus (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB909006676A GB9006676D0 (en) | 1990-03-26 | 1990-03-26 | Sprayable agricultural compositions |
| PCT/GB1991/000451 WO1991014365A1 (fr) | 1990-03-26 | 1991-03-26 | Compositions agricoles pulverisables |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO923732L NO923732L (no) | 1992-09-25 |
| NO923732D0 NO923732D0 (no) | 1992-09-25 |
| NO301148B1 true NO301148B1 (no) | 1997-09-22 |
Family
ID=10673238
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO923732A NO301148B1 (no) | 1990-03-26 | 1992-09-25 | Fremgangsmåte for fremstilling av spröytbare blandinger for jordbruksformål og anvendelse av slike blandinger |
Country Status (13)
| Country | Link |
|---|---|
| EP (1) | EP0521957B1 (fr) |
| AT (1) | ATE176986T1 (fr) |
| AU (1) | AU657680B2 (fr) |
| CA (1) | CA2075809C (fr) |
| DE (1) | DE69130948T2 (fr) |
| DK (1) | DK0521957T3 (fr) |
| ES (1) | ES2127725T3 (fr) |
| FI (1) | FI924321A (fr) |
| GB (1) | GB9006676D0 (fr) |
| GR (1) | GR3029686T3 (fr) |
| NO (1) | NO301148B1 (fr) |
| WO (1) | WO1991014365A1 (fr) |
| ZA (1) | ZA912273B (fr) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9106409D0 (en) * | 1991-03-26 | 1991-05-15 | Allied Colloids Ltd | Sprayable agricultural compositions |
| US5674514A (en) * | 1992-09-21 | 1997-10-07 | Ciba-Geigy Corporation | Storage stable pesticidal aqueous emulsions |
| GB9319112D0 (en) * | 1993-09-15 | 1993-11-03 | Allied Colloids Ltd | Stabilisation and use of heterogeneous liquid composition |
| GB9823752D0 (en) | 1998-10-30 | 1998-12-23 | Allied Colloids Ltd | Compositions comprising anti-drift agents and processes and methods for their use |
| DE19936223A1 (de) | 1999-08-05 | 2001-02-22 | Stockhausen Chem Fab Gmbh | Wirkstoffhaltige Komposition sowie deren Herstellung und Verwendung |
| GB0703394D0 (en) * | 2007-02-22 | 2007-03-28 | Ciba Sc Holding Ag | Process for Preparing and Applying Pesticide or Herbicide Formulation |
| AU2012245869B2 (en) | 2011-04-20 | 2015-12-03 | Indorama Ventures Oxides Llc | Spray drift reduction agents comprising low hydrophilic-lipophilic balance surfactants |
| EP3764787A1 (fr) * | 2018-03-12 | 2021-01-20 | Massachusetts Institute of Technology | Articles et compositions associées à des huiles sur des surfaces et procédés associés |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA785706A (en) * | 1968-05-21 | F. Vartiak Joseph | Herbicidal process | |
| CA1023264A (fr) * | 1973-10-05 | 1977-12-27 | Joseph F. Vartiak | Polymeres latex - herbicides sans brouillard d'entrainement |
| US4126443A (en) * | 1977-11-21 | 1978-11-21 | American Cyanamid Company | Inhibition of crystal formation of 1,2-dimethyl-3,5-diphenylpyrazolium methyl sulfate in aqueous solutions with an acrylamide polymer |
| IL86777A0 (en) * | 1987-06-17 | 1988-11-30 | Nomix Mfg Co Ltd | Plant treatment composition |
| US5321049A (en) * | 1987-10-14 | 1994-06-14 | Dowelanco | Agricultural compositions containing latexes |
-
1990
- 1990-03-26 GB GB909006676A patent/GB9006676D0/en active Pending
-
1991
- 1991-03-26 AT AT91906561T patent/ATE176986T1/de not_active IP Right Cessation
- 1991-03-26 ES ES91906561T patent/ES2127725T3/es not_active Expired - Lifetime
- 1991-03-26 ZA ZA912273A patent/ZA912273B/xx unknown
- 1991-03-26 AU AU75498/91A patent/AU657680B2/en not_active Ceased
- 1991-03-26 DK DK91906561T patent/DK0521957T3/da active
- 1991-03-26 WO PCT/GB1991/000451 patent/WO1991014365A1/fr active IP Right Grant
- 1991-03-26 DE DE69130948T patent/DE69130948T2/de not_active Expired - Fee Related
- 1991-03-26 CA CA002075809A patent/CA2075809C/fr not_active Expired - Fee Related
- 1991-03-26 EP EP91906561A patent/EP0521957B1/fr not_active Expired - Lifetime
-
1992
- 1992-09-25 NO NO923732A patent/NO301148B1/no not_active IP Right Cessation
- 1992-09-25 FI FI924321A patent/FI924321A/fi unknown
-
1999
- 1999-03-12 GR GR990400770T patent/GR3029686T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ATE176986T1 (de) | 1999-03-15 |
| WO1991014365A1 (fr) | 1991-10-03 |
| NO923732L (no) | 1992-09-25 |
| CA2075809A1 (fr) | 1991-09-27 |
| DK0521957T3 (da) | 1999-09-27 |
| AU657680B2 (en) | 1995-03-23 |
| FI924321A0 (fi) | 1992-09-25 |
| FI924321A (fi) | 1992-09-25 |
| DE69130948T2 (de) | 2000-08-17 |
| EP0521957B1 (fr) | 1999-03-03 |
| GB9006676D0 (en) | 1990-05-23 |
| ZA912273B (en) | 1991-12-24 |
| ES2127725T3 (es) | 1999-05-01 |
| EP0521957A1 (fr) | 1993-01-13 |
| DE69130948D1 (de) | 1999-04-08 |
| GR3029686T3 (en) | 1999-06-30 |
| AU7549891A (en) | 1991-10-21 |
| CA2075809C (fr) | 2001-04-24 |
| NO923732D0 (no) | 1992-09-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM1K | Lapsed by not paying the annual fees |
Free format text: LAPSED IN SEPTEMBER 2002 |