EP0381379A1 - Process of offset lithographic printing - Google Patents
Process of offset lithographic printing Download PDFInfo
- Publication number
- EP0381379A1 EP0381379A1 EP19900300790 EP90300790A EP0381379A1 EP 0381379 A1 EP0381379 A1 EP 0381379A1 EP 19900300790 EP19900300790 EP 19900300790 EP 90300790 A EP90300790 A EP 90300790A EP 0381379 A1 EP0381379 A1 EP 0381379A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- paper
- weight
- vinyl
- parts
- emulsion
- 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
- 238000007639 printing Methods 0.000 title claims abstract description 6
- 238000000034 method Methods 0.000 title claims description 7
- 239000000839 emulsion Substances 0.000 claims abstract description 22
- 238000000576 coating method Methods 0.000 claims abstract description 14
- 239000011248 coating agent Substances 0.000 claims abstract description 13
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 12
- 229920001577 copolymer Polymers 0.000 claims abstract description 10
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 10
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 5
- 239000000123 paper Substances 0.000 claims description 26
- 239000000178 monomer Substances 0.000 claims description 17
- 239000008199 coating composition Substances 0.000 claims description 15
- 239000000049 pigment Substances 0.000 claims description 7
- 239000007787 solid Substances 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- 229920001567 vinyl ester resin Polymers 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 239000013530 defoamer Substances 0.000 claims 1
- 239000002270 dispersing agent Substances 0.000 claims 1
- 229920000642 polymer Polymers 0.000 abstract description 6
- 239000000976 ink Substances 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 10
- 239000005977 Ethylene Substances 0.000 description 10
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 7
- 239000000243 solution Substances 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 5
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 4
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 3
- 239000008367 deionised water Substances 0.000 description 3
- 239000004816 latex Substances 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- -1 propylene, butylene Chemical group 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- LRCFXGAMWKDGLA-UHFFFAOYSA-N dioxosilane;hydrate Chemical compound O.O=[Si]=O LRCFXGAMWKDGLA-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 238000000518 rheometry Methods 0.000 description 2
- 229960004029 silicic acid Drugs 0.000 description 2
- BWYYYTVSBPRQCN-UHFFFAOYSA-M sodium;ethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=C BWYYYTVSBPRQCN-UHFFFAOYSA-M 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 1
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 239000004160 Ammonium persulphate Substances 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- 239000004908 Emulsion polymer Substances 0.000 description 1
- XLYMOEINVGRTEX-ARJAWSKDSA-N Ethyl hydrogen fumarate Chemical group CCOC(=O)\C=C/C(O)=O XLYMOEINVGRTEX-ARJAWSKDSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group 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
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 244000089486 Phragmites australis subsp australis Species 0.000 description 1
- 235000014676 Phragmites communis Nutrition 0.000 description 1
- 241001315609 Pittosporum crassifolium Species 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
- 235000019395 ammonium persulphate Nutrition 0.000 description 1
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- ZPOLOEWJWXZUSP-AATRIKPKSA-N bis(prop-2-enyl) (e)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C\C(=O)OCC=C ZPOLOEWJWXZUSP-AATRIKPKSA-N 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- GFJVXXWOPWLRNU-UHFFFAOYSA-N ethenyl formate Chemical compound C=COC=O GFJVXXWOPWLRNU-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- XLYMOEINVGRTEX-UHFFFAOYSA-N fumaric acid monoethyl ester Natural products CCOC(=O)C=CC(O)=O XLYMOEINVGRTEX-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical group O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000001459 lithography Methods 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920005596 polymer binder Polymers 0.000 description 1
- 239000002491 polymer binding agent Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 1
- LGORLCOUTMVEAC-UHFFFAOYSA-M sodium;2-nonylphenolate Chemical compound [Na+].CCCCCCCCCC1=CC=CC=C1[O-] LGORLCOUTMVEAC-UHFFFAOYSA-M 0.000 description 1
- 230000003019 stabilising effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 1
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical class [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 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
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/56—Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H19/60—Polyalkenylalcohols; Polyalkenylethers; Polyalkenylesters
Definitions
- This invention relates to aqueous emulsions containing copolymers of vinyl acetate and ethylene in which vinyl acetate is the major component. Copolymers of the invention are utilised in paper coating compositions and demonstrate good rheology and dry pick strength with enhanced wet pick strength.
- Paper coating compositions usually comprise an aqueous polymer binder emulsion, a pigment and optionally other additives common in the technology.
- the present invention is specifically directed to novel emulsions based on copolymers comprising a vinyl C1 to C4 alkanoate component forming at least about 60% by weight of the copolymer, more usually at least about 70% by weight and an alkylene component, eg. ethylene.
- Vinyl acetate is an example of a vinyl ester of a C1 to C4 alkanoic acid to which the invention is generally directed.
- Coating compositions of the invention will contain a pigment, for example clay, which is compounded with the latex binder and used in coating a cellulosic web for example a paper or paperboard web.
- the characteristics of the latex binder component are significant in the ease of preparation of the paper coating composition, its application and on the qualities of the coated product.
- the coating composition will be coated on to a paper substrate, dried and calendered. Usually the composition will be applied at a level to give a loading of about 18 to about 24 g/m 2 solids on one surface.
- the copolymer particles will bind those of the pigment filler to provide cohesive strength and contribute to the adhesion between the coating and paper substrate.
- the coating which will usually have a thickness of about 3 microns to about 10 microns imparts gloss and whiteness to the paper and provides a suitable surface for receiving ink.
- the coating When the coating is subjected to successive printing operations, for example in offset lithography, the coating must provide acceptable wet and dry pick strengths.
- the first colour When the first colour is printed any pull by the tacky ink giving failure of the coating is termed 'dry pick'.
- the invention provides the use in paper coating of an aqueous copolymer emulsion having a solids content from about 20% to about 70% by weight and comprising
- This product has good rheology and dry pick strength and enhanced wet pick strength which is attributable to the presence of vinyl ester (iii) monomers. There is a general requirement in paper coating to improve these characteristics.
- the invention extends to a pigmented paper coating composition
- a pigmented paper coating composition comprising
- the polymerisation system will be substantially free of protective colloids. Colloidal materials may be added subsequently to the paper coating composition.
- vinyl acetate is the preferred vinyl alkanoate monomer because of its availability, cost and known reactivity
- other vinyl esters within the class defined are usable in particular vinyl formate, propionate. butyrate and isobutyrate.
- the preferred alkylene is ethylene but other ethylenic hydrocarbons, for example propylene, butylene and isobutene are usable.
- the copolymer may contain minor monomer components added to provide specific benefits, examples are sodium vinyl sulphonate, acrylic acid, methacrylic acid, acrylamide, hydroxy functional acrylates, vinyl silanes and vinyl halides.
- a favoured comonomer is a polyethylencially unsaturated compound selected from triallyl cyanurate, triallyl isocyanurate, diallyl maleate, diallyl fumarate, divinyl benzene and diallyl phthalate.
- At least one surfactant used in the polymerisation process contains a C14 to C20 alkylene moiety and examples are an oleyl propanol amide sulphosuccinate obtainable from Witco of USA under the trade name Emcol K8300 and the potassium salt of the sulphonation product of oleic acid obtainable from Lankro Chemicals of Manchester England under the trade name Lankropol OPA.
- the paper coating composition comprises a pigment, for example clays, hydrated silica clays, and other conventional ingredients.
- the clays used include Kaolin group clays and hydrated silica clays, specific clays are disclosed in "Kaolin Clays and their Industrial Uses" by J. M. Huber Corp. (1949) New York chapters 10 to 16.
- pigments for example calcium carbonate, titanium dioxide, blanc fixe, lithopone and zinc sulphide may be used in addition to clay.
- the paper coating composition will comprise
- the coating compositions produced with the aid of the latexes of the invention will be applied to fibrous paper webs using conventional means for example trailing blade coaters, air knife coaters and roll coaters.
- EPA 0295727 (Shell) describes polymer emulsions containing vinyl acetate, ethylene and versatates (Veova 9) for use in paint compositions to give non tacky surfaces which are alkali resistant. These benefits are demonstrated in comparison with Veova 10. The description suggests the emulsions are usable in paper coating and other fields, but there is no disclosure of the wet pick benefit identified in the present application.
- EPA 0172354 Air Products describes vinyl alkanoate/Ethylene emulsions for paper coating which provide enhanced dry pick strength and gloss.
- the additional monomers are unsaturated acids/esters and dicyclopenta-dienyl acrylate. Vinyl versatates are quoted as examples of the alkanoates but there is no suggestion to use them as a third monomer with VA/E. VA/E is stated to lack sufficient wet pick resistance for offset printing.
- GB 1144316 (Dunlop) describes alkali-soluble polymer emulsions formed from quaternary alpha carbon carboxylic, vinyl carboxylate and unsaturated carboxylic monomers. pH and viscosity stability derive from the tertiary monomer.
- the degree of resistance to pick is judged at a qualitative level i.e. good - fair - bad.
- a surfactant solution comprising 37% aq. solution of Emcol K8300 (74.2g), 30% aq solution of Aerosol A102 (53.2g) and ammonium persulphate (4.3g) dissolved in deionised water (999g) was prepared and charged to a 4 litre pressure vessel. The contents are heated to 68 0 C. At 68 0 C the reactor was purged twice with nitrogen, once with ethylene and pressurised with ethylene to 450 Ibs/sqin gauge with stirring. The temperature was adjusted to 76 C while 10% of the liquid monomer phase was pumped to the reactor.
- reaction mass was held at 80 C for 45 mins, at the end of which the addition of persulphate solution was stopped.
- the contents of the reactor was cooled to 40°C, followed by pumping of finishing off stage (4.6g of each in 70g of deionised water) to the reactor, in separate streams, over 30 minutes.
- the contents of the reactor were then cooled to 25" C and discharged to a degassing tank.
- Ammonia solution was used to adjust the pH of the emulsion latex to 8.
- the emulsion had a solids content of 51.6% by wt.
- Example II Additional examples were performed using the process steps of Example I but varying the quantities of the base monomers, i.e. vinyl acetate, VeoVa 9 and ethylene, the functional monomers and the stabilising surfactants. These emulsions were also tested for wet and dry pick strengths.
- the base monomers i.e. vinyl acetate, VeoVa 9 and ethylene
- the functional monomers i.e. vinyl acetate, VeoVa 9 and ethylene
- stabilising surfactants i.e. vinyl acetate, VeoVa 9 and ethylene
- the emulsion products had solids contents comparable to that obtained in Example I.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Paper (AREA)
- Manufacture Or Reproduction Of Printing Formes (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Lubricants (AREA)
- Polymerisation Methods In General (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Paints Or Removers (AREA)
- Steroid Compounds (AREA)
Abstract
Description
- This invention relates to aqueous emulsions containing copolymers of vinyl acetate and ethylene in which vinyl acetate is the major component. Copolymers of the invention are utilised in paper coating compositions and demonstrate good rheology and dry pick strength with enhanced wet pick strength.
- Paper coating compositions usually comprise an aqueous polymer binder emulsion, a pigment and optionally other additives common in the technology. The present invention is specifically directed to novel emulsions based on copolymers comprising a vinyl C1 to C4 alkanoate component forming at least about 60% by weight of the copolymer, more usually at least about 70% by weight and an alkylene component, eg. ethylene. Vinyl acetate is an example of a vinyl ester of a C1 to C4 alkanoic acid to which the invention is generally directed. Coating compositions of the invention will contain a pigment, for example clay, which is compounded with the latex binder and used in coating a cellulosic web for example a paper or paperboard web. The characteristics of the latex binder component are significant in the ease of preparation of the paper coating composition, its application and on the qualities of the coated product.
- The coating composition will be coated on to a paper substrate, dried and calendered. Usually the composition will be applied at a level to give a loading of about 18 to about 24 g/m2 solids on one surface. The copolymer particles will bind those of the pigment filler to provide cohesive strength and contribute to the adhesion between the coating and paper substrate. The coating, which will usually have a thickness of about 3 microns to about 10 microns imparts gloss and whiteness to the paper and provides a suitable surface for receiving ink.
- When the coating is subjected to successive printing operations, for example in offset lithography, the coating must provide acceptable wet and dry pick strengths. When the first colour is printed any pull by the tacky ink giving failure of the coating is termed 'dry pick'. Failure when the coated paper passes to the second inking stage, when ink is applied to prewetted areas, is termed 'wet pick'. Subsequent inking steps can also give rise to wet pick failure.
- The invention provides the use in paper coating of an aqueous copolymer emulsion having a solids content from about 20% to about 70% by weight and comprising
- i) from about 60%, preferably from about 70%, to about 90% by weight of a vinyl C1 to C4 alkanoate,
- ii) from about 5% to about 20% of a C1 to C4 alkylene monomer, and
- iii) from about 5% to about 20% by weight, preferably from about 8% to about 15% by weight, of vinyl esters having the general formula RiR2R3 CCOOCHCH2 wherein RiR2 and R3 are each alkyl groups having at least one carbon atom and R, + R2 + R3 is from 6 to 9.
- This product has good rheology and dry pick strength and enhanced wet pick strength which is attributable to the presence of vinyl ester (iii) monomers. There is a general requirement in paper coating to improve these characteristics.
- The invention extends to a pigmented paper coating composition comprising
- i) to 100 parts of pigment and
- ii) from about 3% to about 30% by dry weight of an aqueous emulsion as defined above.
- In the emulsions prepared for use in paper coatings the polymerisation system will be substantially free of protective colloids. Colloidal materials may be added subsequently to the paper coating composition.
- Although vinyl acetate is the preferred vinyl alkanoate monomer because of its availability, cost and known reactivity, other vinyl esters within the class defined are usable in particular vinyl formate, propionate. butyrate and isobutyrate.
- The preferred alkylene is ethylene but other ethylenic hydrocarbons, for example propylene, butylene and isobutene are usable.
- Optionally the copolymer may contain minor monomer components added to provide specific benefits, examples are sodium vinyl sulphonate, acrylic acid, methacrylic acid, acrylamide, hydroxy functional acrylates, vinyl silanes and vinyl halides. A favoured comonomer is a polyethylencially unsaturated compound selected from triallyl cyanurate, triallyl isocyanurate, diallyl maleate, diallyl fumarate, divinyl benzene and diallyl phthalate.
- Methods for preparing the copolymer emulsions of the invention are well characterised in the literature. Polymer Synthesis (vols I and III) by Sandler & Karo (Academic Press 1974) and Preparative Methods of Polymer Chemistry (2nd Ed) by Sorenson and Campbell (Interscience 1968) provide preparative information. Methoden der Organischen Chemie (Houben-Wey) Band XIV published by George Thieme Verlag Stuttgart (1961) also provides preparative descriptions.
- Preferably at least one surfactant used in the polymerisation process contains a C14 to C20 alkylene moiety and examples are an oleyl propanol amide sulphosuccinate obtainable from Witco of USA under the trade name Emcol K8300 and the potassium salt of the sulphonation product of oleic acid obtainable from Lankro Chemicals of Manchester England under the trade name Lankropol OPA.
- The paper coating composition comprises a pigment, for example clays, hydrated silica clays, and other conventional ingredients. The clays used include Kaolin group clays and hydrated silica clays, specific clays are disclosed in "Kaolin Clays and their Industrial Uses" by J. M. Huber Corp. (1949) New York chapters 10 to 16.
-
- The coating compositions produced with the aid of the latexes of the invention will be applied to fibrous paper webs using conventional means for example trailing blade coaters, air knife coaters and roll coaters.
- The applicants are aware of the following disclosures relating to polymer emulsions.
- EPA 0295727 (Shell) describes polymer emulsions containing vinyl acetate, ethylene and versatates (Veova 9) for use in paint compositions to give non tacky surfaces which are alkali resistant. These benefits are demonstrated in comparison with Veova 10. The description suggests the emulsions are usable in paper coating and other fields, but there is no disclosure of the wet pick benefit identified in the present application.
- EPA 0172354 (Air Products) describes vinyl alkanoate/Ethylene emulsions for paper coating which provide enhanced dry pick strength and gloss. The additional monomers are unsaturated acids/esters and dicyclopenta-dienyl acrylate. Vinyl versatates are quoted as examples of the alkanoates but there is no suggestion to use them as a third monomer with VA/E. VA/E is stated to lack sufficient wet pick resistance for offset printing.
- GB 1144316 (Dunlop) describes alkali-soluble polymer emulsions formed from quaternary alpha carbon carboxylic, vinyl carboxylate and unsaturated carboxylic monomers. pH and viscosity stability derive from the tertiary monomer.
-
- i) Dry pick strength values (cm/sec) were measured using a coating composition on Reeds Aircoat woodfree paper using an IGT Dynamic Pick Tester (AC2 Model) with 25 Kg load and low viscosity ink. The composition tested contained:
- ii) The wet pick strength was measured with the apparatus of the dry pick method. 0.3 mls of ink was applied to each roller and distributed for 15 minutes. A test strip of paper coated with the test composition to a level of 20g/m2 (solids) was placed in the device. The inked roller was contacted with the test strip and adjusted to a printing force of 35 Kgf. A drop of tap water was placed on the test strip immediately in the path of the roller so ink is applied over a layer of water spread by progress of the roller.
- The degree of resistance to pick is judged at a qualitative level i.e. good - fair - bad.
- Examples of the invention will now be given to illustrate but not limit the invention.
- In the examples several functional monomers and surfactants were used and these are represented by abbreviations and letters in the table of results in order to simplify the presentations.
- Functional monomers: A172 is vinyl tris trimethoxy silane obtainable from Union Carbide of USA.
- DAM is diallyl maleate.
- EHM is ethyl hydrogen maleate
- SVS is sodium vinyl sulphonate
- Surfactants: A is sodium nonylphenol 20 EO sulphate obtainable from Lankro Chemicals of Manchester England as Perlankrol RN75.
- B is sodium oleyl propanol amide sulphosuccinate obtainable from Witco of USA as Emcol K8300.
- C is sodium dodecyl benzene sulphonate obtainable from Lankro Chemicals as Arylan SC15.
- D is disodium salt of an ethoxylated alcohol half ester of sulphosuccinic acid obtainable from Cyanamid of Wayne New Jersey USA as Aerosol A102.
- A surfactant solution (initial charge) comprising 37% aq. solution of Emcol K8300 (74.2g), 30% aq solution of Aerosol A102 (53.2g) and ammonium persulphate (4.3g) dissolved in deionised water (999g) was prepared and charged to a 4 litre pressure vessel. The contents are heated to 680 C. At 680 C the reactor was purged twice with nitrogen, once with ethylene and pressurised with ethylene to 450 Ibs/sqin gauge with stirring. The temperature was adjusted to 76 C while 10% of the liquid monomer phase was pumped to the reactor.
- The continuous addition of persulphate solution (5.3g in 300g of deionised water) was begun and the reaction mass was held at 76 C for 45 minutes. At the end of this period, the continuous addition of the remainder (90%) of the monomer phase was started. The persulphate solution was added over 6.5 hours and the monomer phase over 5.0 hours. The pressure was maintained at 450 Ibs/sq in gauge until the desired quantity of ethylene had been reacted, this was after four hours from start of continuous persulphate additon.
- After completion of the addition of monomer, the reaction mass was held at 80 C for 45 mins, at the end of which the addition of persulphate solution was stopped. The contents of the reactor was cooled to 40°C, followed by pumping of finishing off stage (4.6g of each in 70g of deionised water) to the reactor, in separate streams, over 30 minutes.
- The contents of the reactor were then cooled to 25" C and discharged to a degassing tank.
-
- The result of the dry and wet pick tests on a coating composition containing the resulting emulsion are given in Table I.
- Additional examples were performed using the process steps of Example I but varying the quantities of the base monomers, i.e. vinyl acetate, VeoVa 9 and ethylene, the functional monomers and the stabilising surfactants. These emulsions were also tested for wet and dry pick strengths.
- The emulsion products had solids contents comparable to that obtained in Example I.
-
Claims (5)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8901871 | 1989-01-27 | ||
GB898901871A GB8901871D0 (en) | 1989-01-27 | 1989-01-27 | Emulsion polymerisation |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0381379A1 true EP0381379A1 (en) | 1990-08-08 |
EP0381379B1 EP0381379B1 (en) | 1994-10-12 |
Family
ID=10650749
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP90300790A Expired - Lifetime EP0381379B1 (en) | 1989-01-27 | 1990-01-25 | Process of offset lithographic printing |
Country Status (11)
Country | Link |
---|---|
EP (1) | EP0381379B1 (en) |
AT (1) | ATE112716T1 (en) |
AU (1) | AU4965790A (en) |
CA (1) | CA2024810A1 (en) |
DE (1) | DE69013182T2 (en) |
DK (1) | DK0381379T3 (en) |
ES (1) | ES2062325T3 (en) |
FI (1) | FI904628A0 (en) |
GB (1) | GB8901871D0 (en) |
PT (1) | PT92978A (en) |
WO (1) | WO1990008853A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU676654B1 (en) * | 1996-03-27 | 1997-03-13 | Kuraray Co., Ltd. | Paper coating agent |
EP2892718A4 (en) * | 2012-09-10 | 2016-06-08 | Functionalized vinyl acetate ethylene binders for paper and paperboard coatings | |
EP3122935A4 (en) * | 2014-03-27 | 2017-12-06 | Wacker Chemie AG | Aqueous vinyl acetate ethylene copolymer dispersion for paper coating |
US10094068B2 (en) | 2014-03-27 | 2018-10-09 | Wacker Chemical Corporation | Binder for paper coating compositions |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3477871A (en) * | 1965-10-26 | 1969-11-11 | Shell Oil Co | Process for coating paper with a starch-vinyl ester terpolymer latex binder |
US4657821A (en) * | 1983-05-30 | 1987-04-14 | Sumitomo Chemical Co., Ltd. | Paper coating composition |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4503185A (en) * | 1984-06-22 | 1985-03-05 | Air Products And Chemicals, Inc. | Vinyl acetate/ethylene copolymer emulsions for paper coating compositions |
GB8711984D0 (en) * | 1987-05-21 | 1987-06-24 | Shell Int Research | Polymeric products |
-
1989
- 1989-01-27 GB GB898901871A patent/GB8901871D0/en active Pending
-
1990
- 1990-01-25 AU AU49657/90A patent/AU4965790A/en not_active Abandoned
- 1990-01-25 WO PCT/GB1990/000099 patent/WO1990008853A1/en active Application Filing
- 1990-01-25 AT AT90300790T patent/ATE112716T1/en not_active IP Right Cessation
- 1990-01-25 ES ES90300790T patent/ES2062325T3/en not_active Expired - Lifetime
- 1990-01-25 CA CA002024810A patent/CA2024810A1/en not_active Abandoned
- 1990-01-25 DE DE69013182T patent/DE69013182T2/en not_active Expired - Fee Related
- 1990-01-25 DK DK90300790.4T patent/DK0381379T3/en active
- 1990-01-25 EP EP90300790A patent/EP0381379B1/en not_active Expired - Lifetime
- 1990-01-26 PT PT199092978A patent/PT92978A/en not_active Application Discontinuation
- 1990-09-20 FI FI904628A patent/FI904628A0/en not_active Application Discontinuation
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3477871A (en) * | 1965-10-26 | 1969-11-11 | Shell Oil Co | Process for coating paper with a starch-vinyl ester terpolymer latex binder |
US4657821A (en) * | 1983-05-30 | 1987-04-14 | Sumitomo Chemical Co., Ltd. | Paper coating composition |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU676654B1 (en) * | 1996-03-27 | 1997-03-13 | Kuraray Co., Ltd. | Paper coating agent |
EP2892718A4 (en) * | 2012-09-10 | 2016-06-08 | Functionalized vinyl acetate ethylene binders for paper and paperboard coatings | |
EP3122935A4 (en) * | 2014-03-27 | 2017-12-06 | Wacker Chemie AG | Aqueous vinyl acetate ethylene copolymer dispersion for paper coating |
US10094068B2 (en) | 2014-03-27 | 2018-10-09 | Wacker Chemical Corporation | Binder for paper coating compositions |
Also Published As
Publication number | Publication date |
---|---|
WO1990008853A1 (en) | 1990-08-09 |
EP0381379B1 (en) | 1994-10-12 |
GB8901871D0 (en) | 1989-03-15 |
DK0381379T3 (en) | 1994-11-21 |
PT92978A (en) | 1990-07-31 |
ATE112716T1 (en) | 1994-10-15 |
DE69013182T2 (en) | 1995-02-16 |
AU4965790A (en) | 1990-08-24 |
ES2062325T3 (en) | 1994-12-16 |
DE69013182D1 (en) | 1994-11-17 |
CA2024810A1 (en) | 1990-07-28 |
FI904628A0 (en) | 1990-09-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU596878B2 (en) | Printing ink composition | |
US3716504A (en) | Paper coating compositions and products formed therefrom | |
EP0019716B1 (en) | Aqueous polymeric dispersions and paper coating compositions | |
FI72772C (en) | Extremely strong pigment binders intended for paper coating containing carboxylated vinyl ester alkyl acrylate copolymers. | |
US20120021237A1 (en) | Vinyl ester/ethylene-based binders for paper and paperboard coatings | |
US3811933A (en) | Oil and grease resistant paper products and process for treating cellulosic materials | |
US4278583A (en) | Paper coating composition | |
US20160115649A1 (en) | Functionalized vinyl acetate ethylene binders for paper and paperboard coatings | |
US2583274A (en) | Process for producing mineralcoated paper | |
EP0381379B1 (en) | Process of offset lithographic printing | |
US3255130A (en) | Ethylene propylene copolymer latices containing polar groups | |
US3477871A (en) | Process for coating paper with a starch-vinyl ester terpolymer latex binder | |
US4228047A (en) | Starch compatible polyvinyl acetate latices | |
CA1336218C (en) | Emulsion polymerisation | |
US3792128A (en) | Fluoropolymer-carboxylated styrene-butadiene functional surface coating compositions | |
US3409568A (en) | Ethylene/vinyl chloride copolymer pigment binder for coated paper products and process of preparation | |
WO1992001836A2 (en) | Copolymer emulsions for paper coating | |
WO1992001836A1 (en) | Copolymer emulsions for paper coating | |
EP0109463B1 (en) | Polymeric compositions useful as binders in coating colors and coating colors prepared therefrom | |
JPH10298208A (en) | Production of copolymer latex and paper coating composition containing the copolymer latex | |
US5219924A (en) | Process for the production of paper coating binders | |
US3567503A (en) | Paper treated with copolymer compositions | |
JP3148315B2 (en) | Composition for paper coating and coated paper | |
JPH05279406A (en) | Production of copolymer latex and composition containing the same | |
US3632425A (en) | Polymer modified starch compositions |
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: 19901001 |
|
17Q | First examination report despatched |
Effective date: 19920828 |
|
RAP3 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: UNILEVER N.V. Owner name: UNILEVER PLC |
|
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 |
|
REF | Corresponds to: |
Ref document number: 112716 Country of ref document: AT Date of ref document: 19941015 Kind code of ref document: T |
|
REF | Corresponds to: |
Ref document number: 69013182 Country of ref document: DE Date of ref document: 19941117 |
|
REG | Reference to a national code |
Ref country code: DK Ref legal event code: T3 |
|
ITF | It: translation for a ep patent filed | ||
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2062325 Country of ref document: ES Kind code of ref document: T3 |
|
ET | Fr: translation filed | ||
EAL | Se: european patent in force in sweden |
Ref document number: 90300790.4 |
|
REG | Reference to a national code |
Ref country code: GR Ref legal event code: FG4A Free format text: 3014273 |
|
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 | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 19951213 Year of fee payment: 7 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 19951218 Year of fee payment: 7 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GR Payment date: 19951219 Year of fee payment: 7 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: AT Payment date: 19951221 Year of fee payment: 7 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 19951231 Year of fee payment: 7 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DK Payment date: 19960102 Year of fee payment: 7 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 19960111 Year of fee payment: 7 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 19960123 Year of fee payment: 7 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 19960125 Year of fee payment: 7 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 19960207 Year of fee payment: 7 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: CH Payment date: 19960423 Year of fee payment: 7 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Effective date: 19970125 Ref country code: DK Effective date: 19970125 Ref country code: AT Effective date: 19970125 |
|
REG | Reference to a national code |
Ref country code: DK Ref legal event code: EBP |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Effective date: 19970126 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION Effective date: 19970127 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Effective date: 19970131 Ref country code: CH Effective date: 19970131 Ref country code: BE Effective date: 19970131 |
|
BERE | Be: lapsed |
Owner name: UNILEVER N.V. Effective date: 19970131 Owner name: UNILEVER P.L.C. Effective date: 19970131 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GR Free format text: THE PATENT HAS BEEN ANNULLED BY A DECISION OF A NATIONAL AUTHORITY Effective date: 19970731 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Effective date: 19970801 |
|
REG | Reference to a national code |
Ref country code: GR Ref legal event code: MM2A Free format text: 3014273 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 19970125 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Effective date: 19970930 |
|
NLV4 | Nl: lapsed or anulled due to non-payment of the annual fee |
Effective date: 19970801 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Effective date: 19971001 |
|
EUG | Se: european patent has lapsed |
Ref document number: 90300790.4 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 19991201 |
|
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 NON-PAYMENT OF DUE FEES;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. Effective date: 20050125 |