EP0274886B2 - Pressure sensitive record material - Google Patents
Pressure sensitive record material Download PDFInfo
- Publication number
- EP0274886B2 EP0274886B2 EP87311138A EP87311138A EP0274886B2 EP 0274886 B2 EP0274886 B2 EP 0274886B2 EP 87311138 A EP87311138 A EP 87311138A EP 87311138 A EP87311138 A EP 87311138A EP 0274886 B2 EP0274886 B2 EP 0274886B2
- Authority
- EP
- European Patent Office
- Prior art keywords
- coating
- pigment
- record material
- parts
- binder
- 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.)
- Expired - Lifetime
Links
- 239000000463 material Substances 0.000 title claims abstract description 40
- 238000000576 coating method Methods 0.000 claims abstract description 121
- 239000011248 coating agent Substances 0.000 claims abstract description 108
- 239000000049 pigment Substances 0.000 claims abstract description 61
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 49
- 239000011230 binding agent Substances 0.000 claims abstract description 43
- 238000004513 sizing Methods 0.000 claims abstract description 13
- 230000004888 barrier function Effects 0.000 claims abstract description 7
- 239000000203 mixture Substances 0.000 claims description 48
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 39
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 17
- 229920000126 latex Polymers 0.000 claims description 16
- 239000004816 latex Substances 0.000 claims description 16
- 239000002245 particle Substances 0.000 claims description 16
- 239000007787 solid Substances 0.000 claims description 16
- -1 alkyl ketene dimer Chemical compound 0.000 claims description 14
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 10
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 239000000853 adhesive Substances 0.000 claims description 7
- 230000001070 adhesive effect Effects 0.000 claims description 7
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 7
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 7
- 229940105329 carboxymethylcellulose Drugs 0.000 claims description 7
- 230000007935 neutral effect Effects 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- 229940014800 succinic anhydride Drugs 0.000 claims description 6
- 239000002174 Styrene-butadiene Substances 0.000 claims description 5
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 5
- 108090000623 proteins and genes Proteins 0.000 claims description 5
- 102000004169 proteins and genes Human genes 0.000 claims description 5
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 5
- 244000068988 Glycine max Species 0.000 claims description 4
- 235000010469 Glycine max Nutrition 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 229920002635 polyurethane Polymers 0.000 claims description 4
- 239000004814 polyurethane Substances 0.000 claims description 4
- 239000011115 styrene butadiene Substances 0.000 claims description 4
- 235000010443 alginic acid Nutrition 0.000 claims description 3
- 229920000615 alginic acid Polymers 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 229920001477 hydrophilic polymer Polymers 0.000 claims description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 3
- 239000011707 mineral Substances 0.000 claims description 3
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 claims description 2
- 229940072056 alginate Drugs 0.000 claims description 2
- 239000012736 aqueous medium Substances 0.000 claims description 2
- 239000008199 coating composition Substances 0.000 claims description 2
- 239000011236 particulate material Substances 0.000 claims description 2
- 238000000926 separation method Methods 0.000 claims description 2
- 229920001909 styrene-acrylic polymer Polymers 0.000 claims description 2
- 229920006174 synthetic rubber latex Polymers 0.000 claims description 2
- 229920000881 Modified starch Polymers 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 235000019426 modified starch Nutrition 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 15
- 239000004927 clay Substances 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- 238000007639 printing Methods 0.000 description 7
- 239000005995 Aluminium silicate Substances 0.000 description 6
- 229920002472 Starch Polymers 0.000 description 6
- 235000012211 aluminium silicate Nutrition 0.000 description 6
- 235000019698 starch Nutrition 0.000 description 6
- NGDLSKPZMOTRTR-OAPYJULQSA-N (4z)-4-heptadecylidene-3-hexadecyloxetan-2-one Chemical compound CCCCCCCCCCCCCCCC\C=C1/OC(=O)C1CCCCCCCCCCCCCCCC NGDLSKPZMOTRTR-OAPYJULQSA-N 0.000 description 5
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 5
- 230000003287 optical effect Effects 0.000 description 5
- 239000008107 starch Substances 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 239000008116 calcium stearate Substances 0.000 description 4
- 235000013539 calcium stearate Nutrition 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 238000010410 dusting Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000000518 rheometry Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- ORACIQIJMCYPHQ-MDZDMXLPSA-N 2-[4-[(e)-2-[4-(1,3-benzoxazol-2-yl)phenyl]ethenyl]phenyl]-1,3-benzoxazole Chemical compound C1=CC=C2OC(C3=CC=C(C=C3)/C=C/C=3C=CC(=CC=3)C=3OC4=CC=CC=C4N=3)=NC2=C1 ORACIQIJMCYPHQ-MDZDMXLPSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 229910021532 Calcite Inorganic materials 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000005282 brightening Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000661 sodium alginate Substances 0.000 description 2
- 235000010413 sodium alginate Nutrition 0.000 description 2
- 229940005550 sodium alginate Drugs 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- JVKRKMWZYMKVTQ-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]pyrazol-1-yl]-N-(2-oxo-3H-1,3-benzoxazol-6-yl)acetamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C=NN(C=1)CC(=O)NC1=CC2=C(NC(O2)=O)C=C1 JVKRKMWZYMKVTQ-UHFFFAOYSA-N 0.000 description 1
- 241000272165 Charadriidae Species 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 235000019759 Maize starch Nutrition 0.000 description 1
- 108010073771 Soybean Proteins Proteins 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000005354 coacervation Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- XOVJAYNMQDTIJD-UHFFFAOYSA-N cyclopentobarbital Chemical compound C1CC=CC1C1(CC=C)C(=O)NC(=O)NC1=O XOVJAYNMQDTIJD-UHFFFAOYSA-N 0.000 description 1
- WASQWSOJHCZDFK-UHFFFAOYSA-N diketene Chemical compound C=C1CC(=O)O1 WASQWSOJHCZDFK-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 238000013031 physical testing Methods 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229940001941 soy protein Drugs 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/124—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/124—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components
- B41M5/132—Chemical colour-forming components; Additives or binders therefor
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/124—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components
- B41M5/165—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components characterised by the use of microcapsules; Special solvents for incorporating the ingredients
Definitions
- the invention relates to paper for carbonless copy paper sets and to copy paper sets made up using it.
- Carbonless copy paper sets consist of a top sheet known as the CB (coated back) sheet, a back sheet known as the CF (coated front) sheet, and optionally one or more intermediate sheets known as CFB (coated front and back) sheets.
- the coatings of the back of the CB sheet, of the front and back of the CFB sheets if any, and of the front of the CF sheet contain materials that when brought into association with each other develop a coloured image.
- the present invention has arisen from a requirement, in the highest grade products, for a pigment-containing coating on the front face of CB sheets, improving them in appearance and in printability.
- the invention lies in record material comprising a paper CB sheet having on its front a printable pigment coating and on its back isolated droplets of colour former solution each confined within a pressure rupturable barrier, wherein the pigment coating comprises a binder for the pigment together with a synthetic reactive sizing agent and optionally also a coating structure agent.
- the sizing agent is for example an alkyl ketene dimer alkenyl succinic anhydride, or other neutral reactive size. Another example is a polyurethane size.
- the coating structure agent is for example a carboxy methyl cellulose, a soya or other protein, an alginate, or other hydrophilic polymer. The relative amounts of components in the coating are desirably by weight 60 - 95 parts pigment, 10 - 30 parts binder, 0.5 - 10 parts size and 0.5 - 5 parts coating structure agent where present.
- pigment, binder and size are respectively 60 - 95 parts, 16 - 22 parts and 0.5 - 10 parts, or pigment, binder and coating structure agent are respectively 75 - 85 parts, 12 - 22 parts and 0.5 to 5 parts, with in the latter case 1 - 5 parts size being present also.
- the invention further provides
- the binder is present to hold the pigment in a non-dusting, printable coating, and to enable enough binder to be used for that purpose it must be a material that when tested at 40 weight % in water gives a fluid preparation mixable with pigment to give a coatable dispersion. Normally it will be a latex binder but for example hydroxyalkyl ether derivatives of starches are suitable. Auxiliary binder materials may also be included.
- the size is used to hold off latex-based or other edge-padding adhesives to allow form sets to be fanned.
- the coating structure agent is a hydrophilic polymer that provides a Bendtsen porosity of the finished i.e. CB coated sheet of not less than 25 ml/min, preferably more. Such porosities reflect porosities before CB coating of around 30 ml/min or more allowing economic application of the CB coating. Suitable materials are believed to act by gelling the pigment coating in the course of drying, preventing it from compacting into an impermeable layer, and all are materials that when tested in water at 25 weight % or more give a gel-like preparation not mixable with pigment to give a coatable dispersion.
- the pigment coating should not nave any significant colour developing properties. Such properties would give rise to edge staining after sifting or sheeting, and possibly other marking arising from capsule rupture and release of colour former solution.
- a well known use of copy paper sets is in the production of multiple sets or "form sets" as disclosed, for example, in EP-A 8 161.
- repeats of the sequence of sheets, CB, optionally one or more CFB and CF, that constitute an individual set are made up as a stack.
- An adhesive known as an edge padding adhesive, is applied down one side of the stack, its characteristic being that it is attracted to the coating of the back of the CB (and any CFB) sheets, or to the coating of the front of the CF (and any CFB) sheets, or to both, to a greater extent than to what are, conventionally, uncoated faces of the sheets in the stack, which are the fronts of the CB sheets and the backs of the CF sheets.
- edge padding adhesive is applied down one side of the stack, its characteristic being that it is attracted to the coating of the back of the CB (and any CFB) sheets, or to the coating of the front of the CF (and any CFB) sheets, or to both, to a greater extent than to what
- CB front face pigment coating would be thought of as incompatible with edge padding, the coating attracting the edge padding adhesive in the same way as the coatings within the sets.
- the invention overcomes such problems. While of course the use of sizes in paper generally is known, and so is pigment coating and the use of binders to retain the pigment on the paper, there has been no reason to size a pigment coating as such. Indeed a pigment would normally be thought of as incompatible with size, using a lot of it to no purpose, and the success of the combination is surprising.
- CB coatings containing colour former in relatively fragile (usually encapsulated) form, must in practice be applied after the coating of the front of the sheet.
- Application involves use of driving rolls run at high speed with the paper tensioned over them and if air is not to be entrained between paper and roll the paper must have enough permeability for the air to escape. Without it the paper is liable to "hover" on a layer of air over the roll with loss of control of the process and variation in the product.
- Running the coater at a lower speed to avoid the problem is unacceptable for production efficiency.
- Increasing the tension to exclude the air is possible in theory but risks damage to the product, e.g. by more frequent breaks and/or curing or inferior aspect.
- the pigment coating is typically highly consolidated to give a smooth surface.
- the use of these highly consolidated coatings means that the sheet porosity of the paper is very low.
- the adverse effects of this high content of binder are overcome by the presence in the coating mix of the coating structure agent, sufficient permeability for successful subsequent application of CB coatings being obtained.
- the coating structure agent in the coating mix promotes the generation of a relatively porous coating. We believe that this arises because as the coating mix dries, the coating structure agent helps the mix to set or gel before all the water is removed, and that the set or gelled structure is, at least in part, preserved through drying to give a relatively bulky and thus porous coating. That this effect generates a porous coating even at the high binder levels typically used in this invention is very surprising as such binder levels would ordinarily be expected to "blind" the coating.
- the pigments are, generally, conventional paper coating pigments, in particular inorganic or mineral-derived particulate materials.
- Calcium carbonate especially is economic and suitable, giving good whiteness and purity and having good printing characteristics. It may be supplemented with coating clays such as china clay (kaolin), although with large amounts of clay care will be necessary in formulation to achieve satisfactory rheology and stability for successful coating, as will be appreciated by those skilled in the art.
- Suitable pigments besides china clay include calcined clays, titanium dioxide, finely divided silica and talc.
- Calcium carbonate contributes good whiteness and brightness, and high print definition, but on its own tends to give dusting on the surface and may not good good ink receptivity.
- Clay or talc contribute to a good surface finish and give good ink receptivity without dusting but give a less white appearance.
- Ground calcite as the calcium carbonate has high purity (to give whiteness etc. as compared with ground limestone or chalk) without the very high surface of precipitated carbonates, which can be used but are not preferred because of high binder demand arising from small particle size.
- the pigment in the coatings is not such as to have colour developing properties.
- specific colour developer materials such as the clays that are used as the active constituents of many CF coatings.
- Kaolin has been mentioned in the literature as a colour developer but in unmodified form is not so used or suitable, and papercoating grades are essentially non-colour developing. The use of high levels of binder reduces even further or eliminates any minor residual colour developing activity of the raw material.
- the particle size of the pigment is important. The finer the particles are the more effective the pigment is in terms of brightness but, equally, the more the coating is consolidated (thus reducing porosity) and also the more difficult sizing is; a balance is desirable and the range of 1 to 10 microns, advantageously 2 to 5 ⁇ m is preferred.
- Such particle sizes are as measured by a laser particle sizer such as the standard Malvern 3600 E Type. For particles of broadly the same dimensions in any direction, such as those of calcium carbonate, such sizes approximate actual sizes; for flat or elongated particles such as those of coating clays the particles sizes as measured are nominal.
- the laser instrument assesses particle size by measuring the interference pattern arising from diffraction of the laser light illuminating a sample suspension e.g. in water, of the particles. The pattern is manipulated by a computer to give results as particle size by volume, e.g. the volume itself or the diameter of spheres of equal volume.
- Amounts of pigment are given earlier. Small quantities say up to 10% of specialist pigments, for example TiO 2 whitener, can conveniently by included.
- the binder may be selected from among those conventional in themselves in paper coating technology.
- it may be a synthetic rubber latex such as styrene butadiene latex (normally a carboxylated grade to give good dispersibility and stability in water) or styrene acrylic latex.
- styrene butadiene latex normally a carboxylated grade to give good dispersibility and stability in water
- styrene acrylic latex styrene acrylic latex.
- it is also however possible for it to be for example an ether derivative of starch, as already mentioned, and these are not conventional in the sense of being in wide use.
- the size will typically be a neutral reactive size such as an alkyl ketene dimer or alkenyl succinic anhydride with the alkyl or alkenyl groups from C 8 upwards, generally from C 12 upwards, with C 15 - C 18 typical and the upper limit determined, for example C 24 , by mix workability and suitability of the final coating for printing.
- a neutral reactive size such as an alkyl ketene dimer or alkenyl succinic anhydride with the alkyl or alkenyl groups from C 8 upwards, generally from C 12 upwards, with C 15 - C 18 typical and the upper limit determined, for example C 24 , by mix workability and suitability of the final coating for printing.
- Such sizes in which "neutral” connotes effectiveness as sizes at neutral coating mix pH, are effective in small quantities and readily provide acceptable rheology in the coating process, for example blade, roll or slot (extrusion) coating as known per se .
- Other synthetic sizes such as polyurethane sizes may however be used
- the water repellency of the coating is defined in terms of the contact angle taken up by a water droplet on the surface of the coated paper, measured within the drop, which for a size to be suitable is above 70° and advantageously above 90° or 100°.
- a convenient method of determining the contact angle depends on measurement of the observed height and contact width of a droplet of known volume applied to the paper, in particular in a Lorentzen & Wettre No. 28 surface wettability tester. The method is as follows:-
- the coating structure agents that are suitable include in particular carboxy methyl cellulose such as is used in coating technology as a dewatering control.
- Other suitable materials are proteins, such as soya protein, and alginates such as sodium alginate, their essential characteristic being to provide the desired porous mating structure at the low amounts specfied.
- the amounts used, within the overall range, depend on the nature of the material, enough to be effective but not so much as to increase viscosity or modify the rheology to make the mix uncoatable.
- Amounts are typically, weight % on coating: Amounts are typically, weight % on coating: Carboxy methyl cellulose high mol.wt. 0.5-1.5% medium mol.wt. 1-2% low mol.wt. 2-3% Sodium alginate 0.7-1.5% Soya protein 1.5-4%
- agents for example sodium hydroxide or other alkalis such as potassium hydroxide or ammonia for pH adjustment, and further components of the final coating such as optical brightening agents, dispersants for the pigments, lubricants (e.g. calcium stearate) or antifoams.
- Coat weights may conveniently be 2 to 20 g/m 2 , advantageously 3 to 15 g/m 2 . Papers of reduced substance compared to normal, in terms of fibre weight per square metre, may be used compensating in part for the extra cost of the coatings.
- CB coating the Bendtsen porosity of the final product is not less than 25 ml/min and preferably not less than 30 ml/min with (for this product) a typical range of 35 - 50 ml/min.
- "High speed" is ca.500 m/min or above and a preferred lower limit 400/450 m/min.
- a typical range is ca. 600 - 900 m/min and higher speeds e.g. up to 1500 m/min are possible.
- the invention is described broadly above, but most desirably provides a CB sheet with a printable front coat at 2 - 20g/m 2 comprising an inorganic or mineral derived pigment and a latex-derived binder together with a sizing agent, the sizing agent being an alkyl ketene dimer or alkenyl succinic anhydride or other reactive neutral size giving a contact angle of 90° or more.
- a sizing agent being an alkyl ketene dimer or alkenyl succinic anhydride or other reactive neutral size giving a contact angle of 90° or more.
- Preferred proportions of components by weight are pigment 60 - 95 parts, binder 5 - 30 advantageously 16 - 22 and size 0.5 - 10 parts.
- a coating material was prepared from the following components 48.2% solids in water, final pH 9.5. Material Parts by wt. Coating structure agent 0.8 Sodium hydroxide (first batch) 0.2 Calcium carbonate pigment 60.1 China clay pigment 20.0 Latex binder 16.0 Optical brightener 0.8 Sodium hydroxide (remainder) 0.1
- the coating mix so prepared was applied using trailing blade metering to standard base paper of 48 g/m 2 substance for 'Idem' (Trade Mark) CB sheet to give coat weights of 3 to 7 g/m 2 .
- the coated paper was then calendered and its porosity checked and found to be at a suitable figure. It was CB coated at 800 m/min using a 3 roll coater head, solids of the coating mix ca. 24%, constitution of solids:
- the resulting CB sheets had excellent printing characteristics and improved visual appeal and feel in terms of formation and roughness.
- a coating material was prepared from the following components, made up to 3308 Kg with water Component Dry weight (kg) Approx. % of dry weight "Dispex” N40 (40% in water) dispersing agent 3.6 0.2 "Hydrocarb” 70 calcium carbonate pigment 1275 64.5 Sodium hydroxide (30% in water) 2.4 0.12 "Alphatex” calcined kaolin (china clay) pigment 300 15.2 Carboxymethyl cellulose coating structure agent 24 1.2 “Revinex” 98 F10 latex (50% solids in water) 360 18.2 "Nopcote” C104 (50% in water) calcium stearate 10 0.5
- Revinex 98 F10 latex is a carboxylated SBR latex ex Doverstrand Limited. 'Dispex', 'Hydrocarb', 'Alphatex', 'Revinex' and 'Nopcote' are trade marks.
- This coating was applied to a conventional CB base paper containing 'Leucophor' (Trade Mark) LN optical brightener which after checking porosity was given a CB coating as before.
- Examples 1 and 2 were repeated with respectively 2 parts by weight and 24 Kg of 'Aquapel' (Trade Mark) 360 ⁇ 3 neutral C 16 alkyl ketene dimer size (the level used being such as to give a final coating contact angle of 110° Papers of excellent printability and, further, edge paddable with 100% fanning were obtained.
- 'Aquapel' Trade Mark 360 ⁇ 3 neutral C 16 alkyl ketene dimer size
- Example 2 The formulations were made and coated as in Example 1, the calcium carbonate being of 4 microns median particle size, at 3 and 6 g/m 2 ,on the rougher side of 'Idem' base paper as used in Example 1.
- Material Dry parts Mix 1 Calcium carbonate 100 Total Binder 22 55% solids Coating structure agent 1 pH 9.5 Size 2.5 Optical brightener 1 Mix 2 Calcium carbonate 75 Total China clay 25 50% solids Binder 20 pH 9.5 Coating structure agent 1 Size 2.5 Optical brightener 1 Mix 3 Calcium carbonate 50 Total China clay 50 47% solids Binder 20 pH 9.5 Coating structure agent 1 Size 3.7 Optical brightener 1
- form sets were made up using a latex-based adhesive with CB, 2 ⁇ CFB, and CF sheets, the CFB and CF sheets being standard 'Idem' production and the CB sheets being either standard 'Idem' production base, for comparison, or the Mix 1, 2 and 3 papers above. All sets fanned apart 100%. Bonding strengths within sets, on a subjective 1 to 5 scale (too weak, slightly weak, optimum, slightly strong, too strong) were acceptable throughout, the CB-CF bond in particular, though a little less strong with the Mix 1, 2 and 3 papers than with the base, giving no problem through the presence of the front coating.
- the formulations were coated onto base paper as in Example 1, the machine speed being 400 m/min, and measurements made of important properties.
- the following table shows the mix viscosity of the coating mix, together with porosity before and after application of the CB coat, contact angle, and Bendtsen roughness.
- Test Results - Example 8 Example Coat Mix Viscosity (cPs) Porosity before CB (ml/min) Porosity after CB (ml/min) Contact Angle (Degrees after 2 seconds) Roughness (Bendtsen) 8-C 520 31.5 25.0 77.6 119.0 8-2 505 38.3 13.0 79.0 100.0 8-5 800 25.2 26.0 108.9 125.0 8-7 525 27.3 26.5 79.1 132.0 8-10 195 55.2 60.4 89.8 150.0 8-11 102 25.0 23.0 95.8 146.0
- edge padding trials were carried out as before, with bond strengths found normal or slightly low (but still within-specification) CB-CFB and CFB-CF and 100% fan apart.
- Printing trials again carried out as before, gave good results, the ink on this occasion being Bonsfield Constat Black 30862 (Trade Mark). Ink density was good (slightly light in the absence of the coating structure agent), piling was absent, dusting acceptable throughout and in the mix with starch ether binder exceptionally low.
- a coat mix was made up as an Example 8-C but with the Aquapel 360X replaced by 3.6 parts by weight of 'Fibran 71' (Trade Mark) from National Starch & Chemical Co., which is an alkenyl succinic anhydride size, the other components being in relative parts by weight as shown there, and coated as before.
- 'Fibran 71' Trade Mark
- a satisfactory coating was given, the measured contact angle in particular being 104°, well suited to edge padding.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Paper (AREA)
- Color Printing (AREA)
- Adhesive Tapes (AREA)
- Printing Methods (AREA)
- Measurement And Recording Of Electrical Phenomena And Electrical Characteristics Of The Living Body (AREA)
- Investigating Or Analysing Materials By Optical Means (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Duplication Or Marking (AREA)
Abstract
Description
- The invention relates to paper for carbonless copy paper sets and to copy paper sets made up using it.
- Carbonless copy paper sets consist of a top sheet known as the CB (coated back) sheet, a back sheet known as the CF (coated front) sheet, and optionally one or more intermediate sheets known as CFB (coated front and back) sheets. The coatings of the back of the CB sheet, of the front and back of the CFB sheets if any, and of the front of the CF sheet contain materials that when brought into association with each other develop a coloured image.
- When the front of the CB sheet is typed on or otherwise pressure imaged , material is transferred between the back of one sheet and the front of the nest through the set to give rise to the copies required. Usually, a solution of a dye precursor or "colour former" carried on the sheet as isolated droplets each confined within a pressure rupturable barrier is transferred from the back of one sheet to the front of the nest after rupture of the barrier by the applied pressure, and interacts with a "colour developer" present them to give the image.
- All of this is very well known and requires no detailed description and is disclosed, for example, in EP-A 8 161.
- The present invention has arisen from a requirement, in the highest grade products, for a pigment-containing coating on the front face of CB sheets, improving them in appearance and in printability.
- In one aspect the invention lies in record material comprising a paper CB sheet having on its front a printable pigment coating and on its back isolated droplets of colour former solution each confined within a pressure rupturable barrier, wherein the pigment coating comprises a binder for the pigment together with a synthetic reactive sizing agent and optionally also a coating structure agent.
- The sizing agent is for example an alkyl ketene dimer alkenyl succinic anhydride, or other neutral reactive size. Another example is a polyurethane size. The coating structure agent is for example a carboxy methyl cellulose, a soya or other protein, an alginate, or other hydrophilic polymer. The relative amounts of components in the coating are desirably by weight 60 - 95 parts pigment, 10 - 30 parts binder, 0.5 - 10 parts size and 0.5 - 5 parts coating structure agent where present. In options within these ranges, pigment, binder and size are respectively 60 - 95 parts, 16 - 22 parts and 0.5 - 10 parts, or pigment, binder and coating structure agent are respectively 75 - 85 parts, 12 - 22 parts and 0.5 to 5 parts, with in the latter case 1 - 5 parts size being present also.
- The invention further provides
- A. Multiple form sets fannable apart without separation of the sheets within the sets each comprising a CB sheet, a CF sheet and optionally one or more CFB sheets, and carrying an age adding adhesive to join the sheets within the sets and the sets to each other, wherein the CB sheet is of the record material above.
- B. A method of making a record material comprising a paper sheet having on its front a printable pigment coating and on its back isolated droplets of colour former solution each confined within a pressure rupturable barrier, wherein or the purpose of allowing high speed application of the CB coating subsequent to the application of the pigmented coating the paper sheet is coated with a mix containing a binder for the pigment together with a coating structure agent, a synthetic reactive sizing agent being present also, in an aqueous medium at 25 - 75% advantageously 50 - 65% solids by weight of the mix; is dried to give a coated sheet of Bendtsen porosity 25 to 30 ml/min or more; and is coated on the back at 400 to 450 m/min or more with a colour former coating formulation to give said record material.
- The binder is present to hold the pigment in a non-dusting, printable coating, and to enable enough binder to be used for that purpose it must be a material that when tested at 40 weight % in water gives a fluid preparation mixable with pigment to give a coatable dispersion. Normally it will be a latex binder but for example hydroxyalkyl ether derivatives of starches are suitable. Auxiliary binder materials may also be included.
- The size, as discussed further below, is used to hold off latex-based or other edge-padding adhesives to allow form sets to be fanned.
- The coating structure agent, as also discussed further below, is a hydrophilic polymer that provides a Bendtsen porosity of the finished i.e. CB coated sheet of not less than 25 ml/min, preferably more. Such porosities reflect porosities before CB coating of around 30 ml/min or more allowing economic application of the CB coating. Suitable materials are believed to act by gelling the pigment coating in the course of drying, preventing it from compacting into an impermeable layer, and all are materials that when tested in water at 25 weight % or more give a gel-like preparation not mixable with pigment to give a coatable dispersion.
- It will be understood that as the intention is to improve appearance as well as printability, the pigment coating should not nave any significant colour developing properties. Such properties would give rise to edge staining after sifting or sheeting, and possibly other marking arising from capsule rupture and release of colour former solution.
- A well known use of copy paper sets is in the production of multiple sets or "form sets" as disclosed, for exemple, in EP-A 8 161. In these, repeats of the sequence of sheets, CB, optionally one or more CFB and CF, that constitute an individual set are made up as a stack. An adhesive, known as an edge padding adhesive, is applied down one side of the stack, its characteristic being that it is attracted to the coating of the back of the CB (and any CFB) sheets, or to the coating of the front of the CF (and any CFB) sheets, or to both, to a greater extent than to what are, conventionally, uncoated faces of the sheets in the stack, which are the fronts of the CB sheets and the backs of the CF sheets. Thus there is only a weak bond between CB sheets and adjacent CF sheets above them and individual sets can be separated from each other by "fanning" without the sheets within the sets coming apart from each other.
- However a CB front face pigment coating would be thought of as incompatible with edge padding, the coating attracting the edge padding adhesive in the same way as the coatings within the sets. The invention overcomes such problems. While of course the use of sizes in paper generally is known, and so is pigment coating and the use of binders to retain the pigment on the paper, there has been no reason to size a pigment coating as such. Indeed a pigment would normally be thought of as incompatible with size, using a lot of it to no purpose, and the success of the combination is surprising.
- Separate from questions of edge padding is a desirability of high pigment coat weights for the best properties of printability and appearance.
- The requirement however conflicts with ready application of CB coatings. These, containing colour former in relatively fragile (usually encapsulated) form, must in practice be applied after the coating of the front of the sheet. Application involves use of driving rolls run at high speed with the paper tensioned over them and if air is not to be entrained between paper and roll the paper must have enough permeability for the air to escape. Without it the paper is liable to "hover" on a layer of air over the roll with loss of control of the process and variation in the product. Running the coater at a lower speed to avoid the problem is unacceptable for production efficiency. Increasing the tension to exclude the air is possible in theory but risks damage to the product, e.g. by more frequent breaks and/or curing or inferior aspect.
- In conventional pigment coated printing paper, the pigment coating is typically highly consolidated to give a smooth surface. The use of these highly consolidated coatings means that the sheet porosity of the paper is very low. We have however surprisingly found both good binding and permeability, even though the invention uses a high content of binder such as would in itself be expected to give an entirely impermeable coating. The adverse effects of this high content of binder are overcome by the presence in the coating mix of the coating structure agent, sufficient permeability for successful subsequent application of CB coatings being obtained.
- The inclusion of the coating structure agent in the coating mix promotes the generation of a relatively porous coating. We believe that this arises because as the coating mix dries, the coating structure agent helps the mix to set or gel before all the water is removed, and that the set or gelled structure is, at least in part, preserved through drying to give a relatively bulky and thus porous coating. That this effect generates a porous coating even at the high binder levels typically used in this invention is very surprising as such binder levels would ordinarily be expected to "blind" the coating.
- The reason for the success of the invention appears, though such theory is not to be taken as a limitation of the invention itself, to lie in a microporosity arising from early setting or gelling of the coating as referred to above, without excessive loss of binder into the paper, followed by drying out of the water content of the coating without loss of the structure. It does not appear to arise by a multiple micro-cracking of the coating such as is seen in the colour-developer clay coatings used in CF sheets or the CF face of CFB sheets.
- The pigments are, generally, conventional paper coating pigments, in particular inorganic or mineral-derived particulate materials. Calcium carbonate especially is economic and suitable, giving good whiteness and purity and having good printing characteristics. It may be supplemented with coating clays such as china clay (kaolin), although with large amounts of clay care will be necessary in formulation to achieve satisfactory rheology and stability for successful coating, as will be appreciated by those skilled in the art.
- Other suitable pigments besides china clay include calcined clays, titanium dioxide, finely divided silica and talc.
- A mixture of calcium carbonate and china clay, particularly calcined china clay, is preferred. Calcium carbonate contributes good whiteness and brightness, and high print definition, but on its own tends to give dusting on the surface and may not good good ink receptivity. Clay or talc contribute to a good surface finish and give good ink receptivity without dusting but give a less white appearance. Ground calcite as the calcium carbonate has high purity (to give whiteness etc. as compared with ground limestone or chalk) without the very high surface of precipitated carbonates, which can be used but are not preferred because of high binder demand arising from small particle size.
- It will be understood that the pigment in the coatings is not such as to have colour developing properties. To this end the inclusion as pigments of specific colour developer materials, such as the clays that are used as the active constituents of many CF coatings, will be avoided. Kaolin has been mentioned in the literature as a colour developer but in unmodified form is not so used or suitable, and papercoating grades are essentially non-colour developing. The use of high levels of binder reduces even further or eliminates any minor residual colour developing activity of the raw material.
- The particle size of the pigment is important. The finer the particles are the more effective the pigment is in terms of brightness but, equally, the more the coating is consolidated (thus reducing porosity) and also the more difficult sizing is; a balance is desirable and the range of 1 to 10 microns, advantageously 2 to 5 µm is preferred.
- Such particle sizes are as measured by a laser particle sizer such as the standard Malvern 3600 E Type. For particles of broadly the same dimensions in any direction, such as those of calcium carbonate, such sizes approximate actual sizes; for flat or elongated particles such as those of coating clays the particles sizes as measured are nominal. The laser instrument assesses particle size by measuring the interference pattern arising from diffraction of the laser light illuminating a sample suspension e.g. in water, of the particles. The pattern is manipulated by a computer to give results as particle size by volume, e.g. the volume itself or the diameter of spheres of equal volume.
- Amounts of pigment are given earlier. Small quantities say up to 10% of specialist pigments, for example TiO2 whitener, can conveniently by included.
- Within the constraints above, the binder may be selected from among those conventional in themselves in paper coating technology. In particular it may be a synthetic rubber latex such as styrene butadiene latex (normally a carboxylated grade to give good dispersibility and stability in water) or styrene acrylic latex. It is also however possible for it to be for example an ether derivative of starch, as already mentioned, and these are not conventional in the sense of being in wide use.
- The size will typically be a neutral reactive size such as an alkyl ketene dimer or alkenyl succinic anhydride with the alkyl or alkenyl groups from C8 upwards, generally from C12 upwards, with C15 - C18 typical and the upper limit determined, for example C24, by mix workability and suitability of the final coating for printing. Such sizes, in which "neutral" connotes effectiveness as sizes at neutral coating mix pH, are effective in small quantities and readily provide acceptable rheology in the coating process, for example blade, roll or slot (extrusion) coating as known per se. Other synthetic sizes such as polyurethane sizes may however be used. Amounts within the ranges given earlier are typically 1 to 5% dry weight of the coating but more usually 1 to 2% will be used.
- Suitability of sizes will be in terms of water repellency of the coating in an edge padding context. The water repellency of the coating is defined in terms of the contact angle taken up by a water droplet on the surface of the coated paper, measured within the drop, which for a size to be suitable is above 70° and advantageously above 90° or 100°.
- A convenient method of determining the contact angle depends on measurement of the observed height and contact width of a droplet of known volume applied to the paper, in particular in a Lorentzen & Wettre No. 28 surface wettability tester. The method is as follows:-
- i) A drop of water (initial diameter 4 mm volume ca. 3.35 microlitres) is placed on a test strip of paper
- ii) The drop height (h) and width of contact of the drop on the paper (w) are measured on a projected image of the drop using a graticule
- iii) The contact angle is calculated as
- Since the paper will absorb the water slowly the contact angle is taken as that measured 2 seconds after the drop is placed on the paper.
- The coating structure agents that are suitable include in particular carboxy methyl cellulose such as is used in coating technology as a dewatering control. Other suitable materials are proteins, such as soya protein, and alginates such as sodium alginate, their essential characteristic being to provide the desired porous mating structure at the low amounts specfied. The amounts used, within the overall range, depend on the nature of the material, enough to be effective but not so much as to increase viscosity or modify the rheology to make the mix uncoatable.
- Amounts are typically, weight % on coating:
Amounts are typically, weight % on coating: Carboxy methyl cellulose high mol.wt. 0.5-1.5% medium mol.wt. 1-2% low mol.wt. 2-3% Sodium alginate 0.7-1.5% Soya protein 1.5-4% - Other agents, known in themselves may also be present in the mix, for example sodium hydroxide or other alkalis such as potassium hydroxide or ammonia for pH adjustment, and further components of the final coating such as optical brightening agents, dispersants for the pigments, lubricants (e.g. calcium stearate) or antifoams.
- Coat weights may conveniently be 2 to 20 g/m2, advantageously 3 to 15 g/m2. Papers of reduced substance compared to normal, in terms of fibre weight per square metre, may be used compensating in part for the extra cost of the coatings.
- For high speed, high quality (good curl : good aspect) CB coating the Bendtsen porosity of the final product is not less than 25 ml/min and preferably not less than 30 ml/min with (for this product) a typical range of 35 - 50 ml/min. "High speed" is ca.500 m/min or above and a preferred lower limit 400/450 m/min. A typical range is ca. 600 - 900 m/min and higher speeds e.g. up to 1500 m/min are possible.
- Widest convenient range 25 - 75% solids, more usual 30 - 70%, advantageously 50 - 65%. Lower solids give a wetter mix and greater drying requirement which restricts machine speed; higher solids may give mix viscosity/rheology problems.
- The invention is described broadly above, but most desirably provides a CB sheet with a printable front coat at 2 - 20g/m2 comprising an inorganic or mineral derived pigment and a latex-derived binder together with a sizing agent, the sizing agent being an alkyl ketene dimer or alkenyl succinic anhydride or other reactive neutral size giving a contact angle of 90° or more. Preferred proportions of components by weight are pigment 60 - 95 parts, binder 5 - 30 advantageously 16 - 22 and size 0.5 - 10 parts.
- The invention is illustrated in the following, except Examples 1 and 2 which show the use of coating structure agent in the absence of size, the size being added in Examples 3 and 4.
- A coating material was prepared from the following components 48.2% solids in water, final pH 9.5.
Material Parts by wt. Coating structure agent 0.8 Sodium hydroxide (first batch) 0.2 Calcium carbonate pigment 60.1 China clay pigment 20.0 Latex binder 16.0 Optical brightener 0.8 Sodium hydroxide (remainder) 0.1 -
- Place water in a high speed mixing vessel
- Add the dry coating structure agent and stir for 15 minutes at high speed
- Add first batch of NaOH (40% solids)
- Add calcium carbonate and china clay and stir for 30 minutes at high speed
- Check pH and adjust to approximately 10.0 with some of the remaining NaOH
- Reduce the stirring speeds to slow, add the binder and stir for 10 minutes
- Add the optical brightener
- Bring final pH to 9.5 with NaOH
-
- i) The coating structure agent is a medium molecular weight carboxymethyl cellulose.
- ii) The calcium carbonate pigment is a ground calcite, desirable as high-white material economic in cost. Its median particle size is 2.8 µm (2.8 microns).
- iii) The china clay is a fine, white, commercially available coating clay, median particle size 3.3 microns. It acts as a white pigment accordingly, while preserving the advantages of clay coatings generally in terms of coat adhesion and printing characteristics. It gives no unacceptable reduction in the brightness of coating given by the calcium carbonate.
- iv) The binder is a conventional carboxylated styrene-butadiene synthetic latex giving the coating the necessary adhesion as a whole.
- The coating mix so prepared was applied using trailing blade metering to standard base paper of 48 g/m2 substance for 'Idem' (Trade Mark) CB sheet to give coat weights of 3 to 7 g/m2. The coated paper was then calendered and its porosity checked and found to be at a suitable figure. It was CB coated at 800 m/min using a 3 roll coater head, solids of the coating mix ca. 24%, constitution of solids:
- - 70% capsules
- conventional gelatin-based capsules, black-copy colour former formulation in solvent, formed by coacervation encapsulation
- - 20% stilt
- cellulose floc, ungelatinised starch particles or mixture
- - 10% binder
- maize starch
- The resulting CB sheets had excellent printing characteristics and improved visual appeal and feel in terms of formation and roughness.
- Similarity to Example 1, a coating material was prepared from the following components, made up to 3308 Kg with water
Component Dry weight (kg) Approx. % of dry weight "Dispex" N40 (40% in water) dispersing agent 3.6 0.2 "Hydrocarb" 70 calcium carbonate pigment 1275 64.5 Sodium hydroxide (30% in water) 2.4 0.12 "Alphatex" calcined kaolin (china clay) pigment 300 15.2 Carboxymethyl cellulose coating structure agent 24 1.2 "Revinex" 98 F10 latex (50% solids in water) 360 18.2 "Nopcote" C104 (50% in water) calcium stearate 10 0.5 - Revinex 98 F10 latex is a carboxylated SBR latex ex Doverstrand Limited. 'Dispex', 'Hydrocarb', 'Alphatex', 'Revinex' and 'Nopcote' are trade marks.
- This coating was applied to a conventional CB base paper containing 'Leucophor' (Trade Mark) LN optical brightener which after checking porosity was given a CB coating as before. A CB paper of excellent printability as given without problems in the CB coating process.
- Examples 1 and 2 were repeated with respectively 2 parts by weight and 24 Kg of 'Aquapel' (Trade Mark) 360 × 3 neutral C16 alkyl ketene dimer size (the level used being such as to give a final coating contact angle of 110° Papers of excellent printability and, further, edge paddable with 100% fanning were obtained.
- Those are further Examples with coating structure agent and size together, mixes as below, with water to total 3630 parts, i.e. solids of mix = 55%
Component Example 5 Example 6 Wet Parts Dry Parts % Wet Parts Dry Parts % "Hydrocarb" 70 calcium carbonate 1275 1275 63.8 1259 1259 63.0 "Alphatex" calcined kaolin 300 300 15 300 300 15 "Dispex" N40 dispersing agent 9.1 3.6 0.18 9.1 3.6 0.18 CMC (med mol.wt) coating structure agent 24 24 1.2 40 40 2.0 "Aquapel" 360 X 3 size 322.5 24 1.2 322.5 24 1.2 "Revinex" 98F10 latex binder 720 360 18 - - - Dow 620 latex binder - - - 720 360 18 "Nopcote" C104 calcium stearate 20 10 0.5 20 10 0.5 - Procedures for preparation of the coating mix and its application are as in Examples 1 and 2. Measured porosities (Bendtsen) are:
Ex. 5 Ex. 6 Before CB coat 40.2 ca. 40 After 35.4 ca. 35 - The following is again of the use of a coating structure agent and size together, and is in effect six examples in one (three mixes each coated at two levels).
- The formulations were made and coated as in Example 1, the calcium carbonate being of 4 microns median particle size, at 3 and 6 g/m2,on the rougher side of 'Idem' base paper as used in Example 1.
Material Dry parts Mix 1 Calcium carbonate 100 Total Binder 22 55% solids Coating structure agent 1 pH 9.5 Size 2.5 Optical brightener 1 Mix 2 Calcium carbonate 75 Total China clay 25 50% solids Binder 20 pH 9.5 Coating structure agent 1 Size 2.5 Optical brightener 1 Mix 3 Calcium carbonate 50 Total China clay 50 47% solids Binder 20 pH 9.5 Coating structure agent 1 Size 3.7 Optical brightener 1 - The pairs of samples, all of which showed satisfactory porosities, were subjected to physical testing, in comparison to the uncoated base itself, on a number of criteria significant to CB sheet performance.
-
- Base
- 220 ml/min
- 3 g/m2 samples
- 170 ml/min
- 6 g/m2 samples
- 140 ml/min
-
- Base
- 118°
- Mix 1, both samples
- 117°
- Mix 2, both samples
- 116°
- Mix 3, both samples
- 111°
- These are all very good values of above 110° and, it may be noted, do not vary with the coating weight.
- Base
- 19.0 g/m2/min
- Other samples
- 15.5-17.0 g/m2/min
- Values calculated using filters 9, 10, 11, the brightness being given by the filter 11 value.
Brightness Lightness a b Base 87.3 96.96 15.85 -8.81 Coatings 88.5 to 89.1 96.24 16.16 to 16.42 -9.29 to -9.83 +a = redder +b = yellower
-a = greener -b = bluer - Results were taken with the U.V. in. Significant
improvement was seen in reflectance at 440 nm.Sample Coat weight g/m 440 nm Reflectance L D65 a D65 b D65 Base - 88.95 95.54 -0.50 0.32 Run 1 3 91.19 95.19 0.24 -0.67 Run 2 6 92.64 95.60 0.39 -0.74 Run 3 3 91.43 95.31 0.19 -0.65 Run 4 6 92.14 95.61 0.32 -0.52 Run 5 3 91.03 95.85 0.20 0.27 Run 6 6 91.30 95.78 0.29 0.11 - Using Spring A (35 Kgf) and medium oil. Mix 1 and Mix 2 show improvements on the base and Mix 3 approximately equal values to the base, all satisfactory.
- In a printing trial, mix 1, 2 and 3 papers, which had been CB coated with production black copy formulation with control samples from normal production CB, were printed on a Muller-Martini webb offset printing machine using 'Irlam T11392' (Trade Mark) black ink and a speed of 670 rpm (250 m/min). The Mix 1, 2 and 3 papers all showed low dust, with good ink density/intensity, very little set off, and IGT pick very low or not visible.
- In an edge padding trial, form sets were made up using a latex-based adhesive with CB, 2 × CFB, and CF sheets, the CFB and CF sheets being standard 'Idem' production and the CB sheets being either standard 'Idem' production base, for comparison, or the Mix 1, 2 and 3 papers above. All sets fanned apart 100%. Bonding strengths within sets, on a subjective 1 to 5 scale (too weak, slightly weak, optimum, slightly strong, too strong) were acceptable throughout, the CB-CF bond in particular, though a little less strong with the Mix 1, 2 and 3 papers than with the base, giving no problem through the presence of the front coating.
- In a further multi-part example the formulation below was made up as before, first as shown (Example 8-C) then with the following changes, substitutions being weight for weight:-
- Example 8-2
- Mistron Vapour 3 P (Trade Mark) talc as pigment replacing the kaolin clay
- Example 8-5
- Solfarex A 55 (Trade Mark) starch hydroxyalkyl ether as binder replacing latex
- Example 8-7
- Cyclopal A (Trade Mark) anionic modified polyurethane as size replacing the 'Aquapel'
- Example 8-10
- CMC coating structure agent omitted
- Example 8-11
- Procote 400 (Trade Mark) soy protein as coating structure agent replacing the CMC
- Components are given in the order, pigment, binder, other components, not the order of addition used in mix preparation.
Material Description % (w/w) Hydrocarb 70 Calcium carbonate pigment 63.9 Alphatex Calcined kaolin clay pigment 15.0 Dow 620 Styrene butadiene latex binder 18.0 Aquapel 360X Alkyl ketene dimer size 1.2 Finfix 5 Carboxy methyl cellulose coating structure agent 1.2 Nopcote C104 Calcium stearate lubricant 0.5 Dispex N40 Sodium polyacrylate dispersing agent 0.18 Sodium Hydroxide - 0.04 Leucophor LN Optical brightening agent - Solids = 55% - The formulations were coated onto base paper as in Example 1, the machine speed being 400 m/min, and measurements made of important properties. The following table shows the mix viscosity of the coating mix, together with porosity before and after application of the CB coat, contact angle, and Bendtsen roughness.
Test Results - Example 8 Example Coat Mix Viscosity (cPs) Porosity before CB (ml/min) Porosity after CB (ml/min) Contact Angle (Degrees after 2 seconds) Roughness (Bendtsen) 8-C 520 31.5 25.0 77.6 119.0 8-2 505 38.3 13.0 79.0 100.0 8-5 800 25.2 26.0 108.9 125.0 8-7 525 27.3 26.5 79.1 132.0 8-10 195 55.2 60.4 89.8 150.0 8-11 102 25.0 23.0 95.8 146.0 - In addition to the above tests edge padding trials were carried out as before, with bond strengths found normal or slightly low (but still within-specification) CB-CFB and CFB-CF and 100% fan apart. Printing trials, again carried out as before, gave good results, the ink on this occasion being Bonsfield Constat Black 30862 (Trade Mark). Ink density was good (slightly light in the absence of the coating structure agent), piling was absent, dusting acceptable throughout and in the mix with starch ether binder exceptionally low.
- In a further example a coat mix was made up as an Example 8-C but with the Aquapel 360X replaced by 3.6 parts by weight of 'Fibran 71' (Trade Mark) from National Starch & Chemical Co., which is an alkenyl succinic anhydride size, the other components being in relative parts by weight as shown there, and coated as before. A satisfactory coating was given, the measured contact angle in particular being 104°, well suited to edge padding.
Claims (17)
- Record material comprising a paper CB sheet having on its front a printable pigment coating and on its back isolated droplets of colour former solution each confined within a pressure rupturable barrier, wherein the pigment coating comprises a binder for the pigment together with a synthetic reactive sizing agent and optionally also a coating structure agent.
- Record material of claim 1, wherein the sizing agent is an alkyl ketene dimer, alkenyl succinic anhydride or other neutral reactive size.
- Record material of claim 1, wherein the sizing agent is a polyurethane size.
- Record material claimed in any preceding claim wherein the water repellency of the pigment coating, in terms of the contact angle taken up by a water droplet on the surface of the coated paper, is above 90° and advantageously above 100°.
- Record material claimed in any preceding claim wherein the coating structure agent is present and is a carboxy methyl cellulose, a soya or other protein, an alginate, or other hydrophilic polymer.
- Record material claimed in any preceding claim wherein the binder is a synthetic rubber latex binder advantageously a styrene butadiene or styrene acrylic latex.
- Record material claimed in any one of claims 1 to 5 wherein the binder is a hydroxy alkyl ether starch derivative.
- Record material claimed in any preceding claim wherein the relative amounts of components are by weight 60 - 95 parts pigment, 10 - 30 parts binder, 0.5 - 10 parts size and 0.5 - 5 parts coating structure agent where present.
- Record material claimed in claim 8 wherein the relative amounts of pigment, binder and size are respectively 60 - 95 parts, 16 - 22 parts and 0.5 - 10 parts.
- Record material claimed in claim 8 wherein the coating structure agent is present and the relative amounts of pigment, binder, size and coating structure agent are respectively 75 - 85 parts, 12 - 22 parts 1 - 5 parts and 0.5 to 5 parts.
- Record material claimed in any preceding claim, wherein the coat weight of the front coating is 2 to 20 g/m2 advantageously 3 to 15 g/m2.
- Record material claimed in any preceding claim, wherein the pigment comprises an inorganic or mineral-derived particulate material, advantageously calcium carbonate.
- Record material claimed in any preceding claim, wherein the particle size of the pigment is in the range of 1 to 10 microns, advantageously 2 to 5 microns.
- Record material claimed in any preceding claim, wherein the size is an alkyl ketene dimer or alkenyl succinic anhydride with the alkyl or alkenyl groups from C8 upwards advantageously from C12 upwards, and with a maximum of C24.
- Multiple form sets fannable apart without separation of the sheets within the sets each comprising a CB sheet, a CF sheet and optionally one or more CFB sheets, and carrying an edge padding adhesive to join the sheets within the sets and the sets to each other, wherein the CB sheet is of the record material of any of claims 1 to 14.
- A method of making a record material comprising a paper sheet having on its front a printable pigment coating and on its back isolated droplets of colour former solution each confined within a pressure rupturable barrier, wherein for the purpose of allowing high speed application of the CB coating subsequent to the application of the pigmented coating the paper sheet is coated with a mix containing a binder for the pigment together with a coating structure agent, a synthetic reactive sizing agent being present also, in an aqueous medium at 25 - 75% advantageously 50 - 65% solids by weight of the mix; is dried to give a coated sheet or Bendtsen porosity 25 to 30 ml/min or more; and is coated on the back at 400 to 450 m/min or more with a colour former coating formulation to give said record material.
- A method according to claim 16, wherein the components of the pigment coating are such as to give a record material according to any of claims 2 to 14.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT87311138T ATE51586T1 (en) | 1986-12-18 | 1987-12-17 | PRESSURE SENSITIVE RECORDING MATERIAL. |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8630231 | 1986-12-18 | ||
GB868630231A GB8630231D0 (en) | 1986-12-18 | 1986-12-18 | Pressure sensitive record material |
GB878723732A GB8723732D0 (en) | 1987-10-09 | 1987-10-09 | Pressure sensitive record material |
GB8723732 | 1987-10-09 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0274886A1 EP0274886A1 (en) | 1988-07-20 |
EP0274886B1 EP0274886B1 (en) | 1990-04-04 |
EP0274886B2 true EP0274886B2 (en) | 1997-07-02 |
Family
ID=26291712
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP87311138A Expired - Lifetime EP0274886B2 (en) | 1986-12-18 | 1987-12-17 | Pressure sensitive record material |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP0274886B2 (en) |
JP (1) | JP2583118B2 (en) |
AT (1) | ATE51586T1 (en) |
AU (1) | AU613336B2 (en) |
CA (1) | CA1316957C (en) |
DE (3) | DE3762106D1 (en) |
ES (1) | ES2015062T5 (en) |
FI (1) | FI885711A0 (en) |
GB (1) | GB2209355B (en) |
WO (1) | WO1988004614A1 (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2049819T3 (en) * | 1988-07-01 | 1994-05-01 | Wiggins Teape Group Ltd | PRESSURE SENSITIVE COPY PAPER. |
DE3919736C1 (en) * | 1989-06-16 | 1991-01-17 | Feldmuehle Ag, 4000 Duesseldorf, De | |
FR2648395B1 (en) * | 1989-06-19 | 1992-02-21 | Arjomari Prioux | PRESSURE SENSITIVE RECORDING MATERIAL HAVING GOOD PRINTABILITY AND CAPABLE OF SELF-SEPARATING BUNDLES, AS WELL AS A PRESSURE SENSITIVE SELF-COPYING SHEET AND SELF-COPING SHEET SHEET |
ES2042340T3 (en) * | 1990-12-15 | 1993-12-01 | The Wiggins Teape Group Limited | PRESSURE SENSITIVE COPY PAPER. |
WO1993017877A1 (en) * | 1992-03-06 | 1993-09-16 | Nashua Corporation | Xerographable carbonless forms |
GB9213279D0 (en) * | 1992-06-23 | 1992-08-05 | Wiggins Teape Group Ltd | Pressure sensitive copying paper |
US5885340A (en) * | 1994-10-14 | 1999-03-23 | Ecc International Ltd. | Quality of multiple coated paper |
GB2293991B (en) * | 1994-10-14 | 1998-06-10 | Ecc Int Ltd | Improving the quality of coated paper |
ES2199089B1 (en) * | 2003-09-03 | 2005-08-16 | Signe, S.A. | AUTOCOPIATIVE SECURITY PAPER. |
GB0324755D0 (en) | 2003-10-23 | 2003-11-26 | Arjo Wiggins Ltd | Pressure sensitive record material |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1051661A (en) * | ||||
BE546398A (en) * | 1955-04-27 | 1900-01-01 | ||
FR1353522A (en) * | 1962-12-29 | 1964-02-28 | L Delplanque & Fils Ets | Process of duplicating bundled documents without inserting carbon paper |
US3393925A (en) * | 1963-02-11 | 1968-07-23 | Calvert Bertram | Paper products and method of producing same |
JPS5312844B2 (en) * | 1973-03-22 | 1978-05-04 | ||
DE2400490C2 (en) * | 1974-01-05 | 1982-06-03 | Akzo Gmbh, 5600 Wuppertal | Cationic polyurethanes and processes for their manufacture |
GB2031797B (en) * | 1978-07-26 | 1982-04-07 | Appleton Paper Inc | Process for making pressure-sensitive copying sets |
CA1136305A (en) * | 1978-07-26 | 1982-11-23 | William J. Becker | Adhesive composition for making form sets from carbonless copy paper sheets |
US4446174A (en) * | 1979-04-27 | 1984-05-01 | Fuiji Photo Film Company, Ltd. | Method of ink-jet recording |
CA1186574A (en) * | 1980-08-20 | 1985-05-07 | Mutsuaki Murakami | Ink jet recording sheet |
US4397483A (en) * | 1980-10-17 | 1983-08-09 | Mitsubishi Paper Mills, Ltd. | Pressure sensitive recording paper |
EP0199874A1 (en) * | 1985-02-25 | 1986-11-05 | The Mead Corporation | Ink jet recording sheet having an ink-receptive layer containing polyethylene oxide |
-
1987
- 1987-12-16 CA CA000554742A patent/CA1316957C/en not_active Expired - Lifetime
- 1987-12-17 JP JP63500586A patent/JP2583118B2/en not_active Expired - Lifetime
- 1987-12-17 ES ES87311138T patent/ES2015062T5/en not_active Expired - Lifetime
- 1987-12-17 DE DE8787311138T patent/DE3762106D1/en not_active Expired - Lifetime
- 1987-12-17 AU AU10507/88A patent/AU613336B2/en not_active Expired
- 1987-12-17 AT AT87311138T patent/ATE51586T1/en active
- 1987-12-17 DE DE19873790830 patent/DE3790830T1/de not_active Ceased
- 1987-12-17 EP EP87311138A patent/EP0274886B2/en not_active Expired - Lifetime
- 1987-12-17 DE DE198787311138T patent/DE274886T1/en active Pending
- 1987-12-17 WO PCT/GB1987/000910 patent/WO1988004614A1/en active Application Filing
-
1988
- 1988-10-31 GB GB8825451A patent/GB2209355B/en not_active Expired - Fee Related
- 1988-12-09 FI FI885711A patent/FI885711A0/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
FI885711L (en) | 1988-12-09 |
JP2583118B2 (en) | 1997-02-19 |
AU1050788A (en) | 1988-07-15 |
ES2015062T5 (en) | 1997-10-01 |
ES2015062B3 (en) | 1990-08-01 |
EP0274886A1 (en) | 1988-07-20 |
FI885711A0 (en) | 1988-12-09 |
GB2209355A (en) | 1989-05-10 |
EP0274886B1 (en) | 1990-04-04 |
AU613336B2 (en) | 1991-08-01 |
JPH01500895A (en) | 1989-03-30 |
WO1988004614A1 (en) | 1988-06-30 |
CA1316957C (en) | 1993-04-27 |
ATE51586T1 (en) | 1990-04-15 |
GB2209355B (en) | 1991-06-12 |
GB8825451D0 (en) | 1989-01-05 |
DE3790830T1 (en) | 1988-12-08 |
DE274886T1 (en) | 1988-11-24 |
DE3762106D1 (en) | 1990-05-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU663797B2 (en) | An ink jet recording paper and a manufacturing process thereof | |
US4478910A (en) | Ink jet recording paper | |
EP2588324B1 (en) | Paper for ink-jet recording | |
EP0377983B2 (en) | Newsprint | |
EP0274886B2 (en) | Pressure sensitive record material | |
JPS59204662A (en) | Calcium carbonate, manufacture and use as pigment for gravure coated paper | |
JPS5872495A (en) | Ink jet recording paper | |
JPH05254240A (en) | Pressure-sensitive recording paper | |
US4639751A (en) | Image-receiving sheet for heat transfer recording system | |
US4962072A (en) | Pressure sensitive record material | |
EP1675729B1 (en) | Pressure sensitive record material | |
ZA200306262B (en) | Coated paper with silky feel | |
EP0806300A2 (en) | Ink jet recording paper | |
CA2354329C (en) | Polyethylene glycol-containing paper | |
CA2060892A1 (en) | Upper sheet for carbon-copy system | |
JPS6120797A (en) | Recording paper having excellent ink acceptability | |
JPH02136279A (en) | Ink jet recording sheet | |
JP4496906B2 (en) | Inkjet recording medium | |
JPH0717127A (en) | Inkjet recording sheet | |
JPH08199495A (en) | Cast-coated paper for aqueous gravure printing | |
JP3284536B2 (en) | Pressure-sensitive recording paper | |
JP3328521B2 (en) | Process for producing matte coated paper and matte coated paper | |
JPH0276774A (en) | Ink jet recording sheet | |
JP3028720B2 (en) | Inkjet recording paper | |
JPH0768921A (en) | Ink jet recording sheet and manufacturing method thereof |
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 ES FR GB IT LI NL SE |
|
ITCL | It: translation for ep claims filed |
Representative=s name: JACOBACCI CASETTA & PERANI S.P.A. |
|
17P | Request for examination filed |
Effective date: 19880701 |
|
EL | Fr: translation of claims filed | ||
DET | De: translation of patent claims | ||
17Q | First examination report despatched |
Effective date: 19890512 |
|
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 ES FR GB IT LI NL SE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: AT Effective date: 19900404 Ref country code: NL Effective date: 19900404 Ref country code: SE Effective date: 19900404 |
|
REF | Corresponds to: |
Ref document number: 51586 Country of ref document: AT Date of ref document: 19900415 Kind code of ref document: T |
|
ITF | It: translation for a ep patent filed | ||
REF | Corresponds to: |
Ref document number: 3762106 Country of ref document: DE Date of ref document: 19900510 |
|
ET | Fr: translation filed | ||
NLV1 | Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents act | ||
PLBI | Opposition filed |
Free format text: ORIGINAL CODE: 0009260 |
|
26 | Opposition filed |
Opponent name: PAPIERFABRIK AUGUST KOEHLER AG Effective date: 19901228 Opponent name: A. AHLSTROEM CORPORATION Effective date: 19901228 Opponent name: ZANDERS FEINPAPIERE AG Effective date: 19901222 |
|
ITTA | It: last paid annual fee | ||
APAC | Appeal dossier modified |
Free format text: ORIGINAL CODE: EPIDOS NOAPO |
|
APAC | Appeal dossier modified |
Free format text: ORIGINAL CODE: EPIDOS NOAPO |
|
PLAW | Interlocutory decision in opposition |
Free format text: ORIGINAL CODE: EPIDOS IDOP |
|
PUAH | Patent maintained in amended form |
Free format text: ORIGINAL CODE: 0009272 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: PATENT MAINTAINED AS AMENDED |
|
27A | Patent maintained in amended form |
Effective date: 19970702 |
|
AK | Designated contracting states |
Kind code of ref document: B2 Designated state(s): AT BE CH DE ES FR GB IT LI NL SE |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: AEN Free format text: AUFRECHTERHALTUNG DES PATENTES IN GEAENDERTER FORM |
|
ITF | It: translation for a ep patent filed | ||
ET3 | Fr: translation filed ** decision concerning opposition | ||
REG | Reference to a national code |
Ref country code: CH Ref legal event code: NV Representative=s name: ANDRE BRAUN PATENTANWALT VSP |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: DC2A Kind code of ref document: T5 Effective date: 19970808 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: 732E |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: NV Representative=s name: JACOBACCI & PERANI S.A. Ref country code: CH Ref legal event code: PUE Owner name: THE WIGGINS TEAPE GROUP LIMITED TRANSFER- ARJO WIG |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: TP |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: PC2A |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
APAH | Appeal reference modified |
Free format text: ORIGINAL CODE: EPIDOSCREFNO |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20061113 Year of fee payment: 20 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20061114 Year of fee payment: 20 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: CH Payment date: 20061116 Year of fee payment: 20 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20061124 Year of fee payment: 20 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 20061204 Year of fee payment: 20 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 20061213 Year of fee payment: 20 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: IT Payment date: 20061231 Year of fee payment: 20 |
|
BE20 | Be: patent expired |
Owner name: *ARJO WIGGINS LTD Effective date: 20071217 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: PE20 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20071218 |
|
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: 20071218 Ref country code: GB Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION Effective date: 20071216 |