EP1102819A1 - Additives for printing inks that provide release - Google Patents
Additives for printing inks that provide releaseInfo
- Publication number
- EP1102819A1 EP1102819A1 EP99911311A EP99911311A EP1102819A1 EP 1102819 A1 EP1102819 A1 EP 1102819A1 EP 99911311 A EP99911311 A EP 99911311A EP 99911311 A EP99911311 A EP 99911311A EP 1102819 A1 EP1102819 A1 EP 1102819A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- ink
- sheet
- lithographic
- additive
- range
- 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.)
- Withdrawn
Links
- 239000000976 ink Substances 0.000 title claims abstract description 194
- 239000000654 additive Substances 0.000 title claims abstract description 62
- 238000007639 printing Methods 0.000 title claims abstract description 58
- 230000000996 additive effect Effects 0.000 claims abstract description 36
- -1 poly(dimethylsiloxane) Polymers 0.000 claims abstract description 23
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 14
- 239000000203 mixture Substances 0.000 claims abstract description 13
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 12
- 125000003282 alkyl amino group Chemical group 0.000 claims abstract description 12
- 125000002877 alkyl aryl group Chemical group 0.000 claims abstract description 12
- 125000003118 aryl group Chemical group 0.000 claims abstract description 12
- 239000001257 hydrogen Substances 0.000 claims abstract description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 12
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 12
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims abstract description 10
- 229920001577 copolymer Polymers 0.000 claims abstract description 9
- 125000005647 linker group Chemical group 0.000 claims abstract description 6
- 239000000853 adhesive Substances 0.000 claims description 37
- 230000001070 adhesive effect Effects 0.000 claims description 37
- 239000000758 substrate Substances 0.000 claims description 21
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 16
- 125000003709 fluoroalkyl group Chemical group 0.000 abstract 2
- 238000012546 transfer Methods 0.000 description 28
- 229920001296 polysiloxane Polymers 0.000 description 19
- 239000000123 paper Substances 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 15
- 239000011248 coating agent Substances 0.000 description 14
- 238000000576 coating method Methods 0.000 description 14
- 238000000034 method Methods 0.000 description 14
- 238000012360 testing method Methods 0.000 description 13
- 238000011109 contamination Methods 0.000 description 10
- 230000008569 process Effects 0.000 description 10
- 230000003993 interaction Effects 0.000 description 9
- 240000007124 Brassica oleracea Species 0.000 description 7
- 239000001993 wax Substances 0.000 description 6
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 5
- 229920001223 polyethylene glycol Polymers 0.000 description 5
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 5
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- 238000001723 curing Methods 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 241000779745 Backhousia myrtifolia Species 0.000 description 3
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical group SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 3
- 229920006362 Teflon® Polymers 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000001419 dependent effect Effects 0.000 description 3
- 239000004205 dimethyl polysiloxane Substances 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- 125000003396 thiol group Chemical group [H]S* 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 238000003848 UV Light-Curing Methods 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 239000003317 industrial substance Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- WPPDXAHGCGPUPK-UHFFFAOYSA-N red 2 Chemical compound C1=CC=CC=C1C(C1=CC=CC=C11)=C(C=2C=3C4=CC=C5C6=CC=C7C8=C(C=9C=CC=CC=9)C9=CC=CC=C9C(C=9C=CC=CC=9)=C8C8=CC=C(C6=C87)C(C=35)=CC=2)C4=C1C1=CC=CC=C1 WPPDXAHGCGPUPK-UHFFFAOYSA-N 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 241000501105 Aeshnidae Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- ONTQJDKFANPPKK-UHFFFAOYSA-L chembl3185981 Chemical compound [Na+].[Na+].CC1=CC(C)=C(S([O-])(=O)=O)C=C1N=NC1=CC(S([O-])(=O)=O)=C(C=CC=C2)C2=C1O ONTQJDKFANPPKK-UHFFFAOYSA-L 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- VPWFPZBFBFHIIL-UHFFFAOYSA-L disodium 4-[(4-methyl-2-sulfophenyl)diazenyl]-3-oxidonaphthalene-2-carboxylate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC(C)=CC=C1N=NC1=C(O)C(C([O-])=O)=CC2=CC=CC=C12 VPWFPZBFBFHIIL-UHFFFAOYSA-L 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000011067 equilibration Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- ZYMKZMDQUPCXRP-UHFFFAOYSA-N fluoro prop-2-enoate Chemical class FOC(=O)C=C ZYMKZMDQUPCXRP-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- UJMBCXLDXJUMFB-UHFFFAOYSA-K trisodium;5-oxo-1-(4-sulfonatophenyl)-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazole-3-carboxylate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-UHFFFAOYSA-K 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/101—Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing
Definitions
- This invention relates to printing inks, particularly to additives for printing inks that provide a low energy surface and articles using printing inks with additives.
- Repositionable note pads, tapes and linerless labels typically consist of sheets of stock (paper, films, etc.) coated with pressure sensitive adhesive ("PSA") (and optionally a primer) on one side of the sheet and a release coating (also referred to as "low adhesion backsize” or “LAB”) on the other side.
- PSA pressure sensitive adhesive
- LAB low adhesion backsize
- the release coating is in contact with the adhesive.
- the release coating is used to lower the force required to remove the adhesive from the adjacent sheet in order to facilitate dispensing and minimize stock deformation or curl.
- the release coating is used to ensure easy unwind during processing and dispensing.
- Lithographic, flexographic, or gravure printing processes are often used to prepare printed repositionable notes, tapes and linerless labels. Often, the printing process is separate from and subsequent to the process that applies the adhesive and release coating. In such situations, a roll of stock that has been pre-coated with adhesive and a release material is routed through a printing press, ink is printed on top of the release coating, and the printed material is immediately either rolled back up or cut into a stack of discrete sheets. Printing of ink over the release coating renders the release coating ineffective.
- organopolysiloxanes that contain mercapto groups to lithographic inks in order to improve the properties of printed PSA products such as repositionable notes, tapes and linerless labels. It would be advantageous to have ink that would not form undesirable adhesive-ink interactions, and, preferably, would act as a release material. Such ink would eliminate the aforementioned problems of poor release and high "ink transfer" and allow for the manufacture of improved (better release, less ink transfer) printed repositionable notes, tapes and linerless labels.
- releasable lithographic inks that provide release characteristics to printed inks comprising (a) UV-curable or air-curable printing inks and (b) a release additive.
- the preferred additives to the UV- curable or air-curable inks are mercaptopolydiorganosiloxane copolymers.
- Inks containing additives such as mercaptopolydiorganosiloxane copolymers can be advantageously used in products that have pressure sensitive adhesives (PSAs) in contact with the printed inks in order to reduce undesirable PSA/ink interactions.
- PSAs pressure sensitive adhesives
- Undesirable PSA/ink interactions that are avoided by this invention include "ink transfer" from the printed image to the adhesive which results in damage to the printed image and adhesive contamination, and high release forces during unwind or sheet removal which can cause damage to the backing or render the product unusable.
- Another class of additives that provide good properties for UV-curable inks are acrylate terminated silicones ("silicone macromers").
- Silicone "Plus” HG-10 Siloxane which is commercially available from 3M Company , St. Paul, MN.
- Silicone "Puls” HG-10 is a methacrylate terminated poly(dimethylsilicone) polymer having a number average molecular weight of 10,000.
- adhesive coated articles comprising (a) a backing substrate having a front and back surface, (b) a layer of pressure sensitive adhesive on at least one portion of the back surface of the backing substrate, and (c) indicia on the front surface of the backing substrate, wherein the indicia is printed using lithographic inks having release characteristics.
- a pad assembly comprising a multiplicity of flexible sheets each having similarly sized body portion that have pressure sensitive adhesive on the back surface and indicia printed on the front surface, wherein the indicia is printed with lithographic inks having release characteristics, such that when a sheet is removed from the pad assembly, the sheet is easily removable and the lithographic ink is not transferred from the front of the sheet of a first sheet to the back of the sheet of second sheet overlaying the first sheet.
- the multiplicity of sheets have pressure sensitive adhesive coated onto the back surface of the sheets and the sheets are disposed in a stack with the corresponding peripheral edges of the body portions of the sheets aligned and the pressure sensitive adhesive of each sheet adhering that sheet to the adjacent sheet in the stack.
- Such products include printed repositionable note pads (such as 3M Post-it® Notes), linerless labels, printed pressure sensitive tapes, adhesive coupons, and the like.
- lithographic inks having release characteristics provides a construction that eliminates the need of providing a release coating on sheets having indicia printed on the front of them.
- a method of using lithographic inks having release characteristics are providing comprising the steps of:
- ink additives have been discovered that eliminate the aforementioned problems of poor release and high "ink transfer".
- the additives can be blended with commercially available UV or air-curable lithographic inks and the resultant inks printed on standard lithographic printing presses.
- the mercapto group of the additive enters into the curing processes of both air-curable and UV-curable lithographic inks and becomes covalently bound to the cured ink.
- the bound additive will not transfer to and contaminate pressure sensitive adhesives that may come in contact with the ink.
- Preferred additives are mercaptopolydiorganosiloxane copolymers that are described by the following general formula
- Ri, R 2 and R 3 are monovalent moieties that can independently be the same or different and are selected from the group consisting of alkyl, aryl, alkaryl, alkoxy, alkylamino, hydroxyl, hydrogen, fiuoroalkyl, divalent linking groups and are most preferably alkyl moieties;
- R 4 , R 5 , and Re are monovalent moieties that can independently be the same or different and are selected from the group consisting of alkyl, aryl, alkaryl, alkoxy, alkylamino, hydroxyl, hydrogen, fiuoroalkyl, and are most preferably alkyl moieties;
- z can range from 1 to about 16, preferably from 1 to 5 and is most preferably 3.
- x and y are integers of at least one and the sum of x + y is an integer of 10 or greater.
- the molecular weight of the additive can range from about 1000 to about 200,000.
- the preferable range is from about 5000 to about 50,000.
- the additive has a viscosity which is desirable for blending into inks.
- the molecular weight can also affect additive effectiveness. Optimal molecular weights will be dependent on additive and ink type.
- any cyclic material that may be present is removed prior to use by such methods as evaporation under vacuum at elevated temperatures (for example, 150°C, 200 mm Hg).
- Additional most preferred additives of varying values of R, x, y and z are available from Huls America Inc. (Piscataway, NJ).
- the additive is added to the ink in amounts ranging from 0.1 to 15% by weight of the ink and most preferably between 1 and 5%.
- the optimum additive amount will be dependent on the strength of the pressure sensitive adhesive and desired release value in the printed product. Addition of too much additive can cause wetting problems on the print rollers and blankets and adversely affect the printing process.
- the upper limit of additive ranges between about 5 and 15% depending on the printing press type, roller and blanket materials, and ink formulation.
- the mercapto content (weight percent SH moieties based on weight of additive) in the additive can range from about 0.1 to about 20 weight percent. Most preferable mercapto contents range from 0.35 to about 4 weight %. Additive effectiveness appears to decrease at very high levels of SH. For example, poly(mercaptopropylmethylsiloxane) (26 wt% SH) is not a very effective additive.
- acrylate terminated silicones (“silicone macromers”).
- Silicone "Plus” HG-10 Siloxane which is commercially available from 3M Company , St. Paul, MN.
- Silicone "Puls” HG-10 is a mefhacrylate terminated poly(dimethylsilicone) polymer having a number average molecular weight of 10,000.
- Preferable lithographic inks are curable by UV irradiation although lithographic inks that are curable by air-oxidation may also be used. Typical lithographic inks that are commercially available from common ink suppliers can be used.
- Suitable UV-curable lithographic inks include UV 1/D process inks from Kohl and Madden Corporation (Minneapolis, MN), and UVALUX process inks from Zeller Interchem Corporation (2205 Tomlynn Street, Richmond, VA 23230).
- Standard lithographic printing presses can be used. Such presses for air-curable inks include: Didde's (Emporia, Kansas) Webcom and Apollo presses and printing presses available from Stevens International (Fort Worth, Texas). Laboratory presses include the Little Joe Proving Press (Little Joe Color Swatcher, Somerville, NJ). UV Presses include those available from Sanden (Cambridge, Ontario) and Mueller Martini (New York).
- Additives were added to the base ink and mixed with a wood applicator until uniform. The amount of additive is reported as weight % based on the mass of base ink used.
- Printing was carried out using a Little Joe Lithographic Proving Press (Little Joe Color Swatcher, Somerville, NJ) according to the following procedure. Brayers and print blankets designed specifically for either air-curable or UV-curable inks were used.
- Print #2 was discarded. Prints 3-6 were retained and evaluated.
- each printed sample was immediately attached to a piece of cardboard and passed through an ultraviolet curing unit (Fusion UV Curing Systems, Rockville, MD, F300 ultraviolet lamp system, MC-6R conveyor) at a speed of approximately 15 feet (4.57 meters) per minute.
- an ultraviolet curing unit Fusion UV Curing Systems, Rockville, MD, F300 ultraviolet lamp system, MC-6R conveyor
- the proving press was thoroughly cleaned prior to the printing of another sample. Samples were tested after equilibration in a controlled temperature and humidity room for at least 24 hours.
- This test is similar to TAPPI test method UM-504.
- a 25 mm wide strip of 3M 810 MagicTM Tape was applied to a substrate.
- a 2 kg roller was rolled over the tape on the substrate (two passes) in order to adhere the tape to the substrate.
- One end of the tape was attached to a tensile tester. The tape was peeled from the surface at a 90 degree angle at
- Re-Adhesion is a qualitative measure of the amount of adhesive contamination that occurs when 3M 810 MagicTM Tape is peeled from a substrate.
- the tape that was used in the Peel Adhesion test is applied to the non-adhesive side of unprinted Post- it® Note paper (yellow Ashdown paper). Peel Adhesion was measured and the tape strip was retained for evaluation of ink transfer. The test was carried out on prints 3-6. The average of these tests is reported. The "re-adhesion value" was compared to the Peel
- Sheet removal force is the force required to remove the top sheet from a pad of repositionable notes such as Post-it® Notes. This test was carried out by cutting a one inch (2.54 cm) wide strip across the top sheet of the note pad such that the strip was perpendicular to the adhesive stripe. The adhesive-free end of the strip was attached to a tensile tester. The strip was peeled from the surface at a 90 degree angle at 12" (30.48 cm)/min. The force in g/1" (2.54 cm) was recorded. The test was repeated and the average of the trials was reported.
- Comparative examples C1-C3 showed the detrimental effect of printing a typical air-curable lithographic ink onto a paper coated with a release coating.
- Re-adhesion values were significantly lower (117 and 105 g/1.25" (3.175 cm)) than 140 g/1.25" (3.175 cm), which indicates that contamination of the adhesive with ink was significant. Ink transfer was high (2.5) for both C2 and C3.
- Comparative Examples C4-C12 Comparative examples C4-C6 (Table 1) showed that use of typical ink additives such as polyethylene and polytetrafluoroethylene (such as Teflon®) waxes did not improve release and cause adhesive contamination as indicated by the high peel adhesion and low re-adhesion values. Comparative examples C7-C12 showed that stearic acid, fluorine containing monomers, a methacrylate terminated silicone "silicone macromer", and polyethylene glycol monomethacrylate also provided poor results. JM410-9, 410-8, and 413-3 are typical waxes that are used in lithographic inks.
- JM410-9 is commercially available as "Super Poly 4" from Lawter International, pleasant, WI.
- JM410-8 is commercially available as "CC5510-D” and JM413-3 is commercially available as "PROTECH 200" both materials are available from Carrol Scientific, Countryside, LL.
- CW-750 is polyethylene glycol monomethacrylate 10 moles, EO obtained from Polysciences, Inc., Warrington, PA (Cat. #16713).
- Comparative examples C13 and C14 showed that using mercaptan-free polydimethylsiloxanes that did not have mercaptan functionality did not provide improved properties.
- polydimethylsiloxane trimethylsiloxy terminated, CAS No. [63148-62-9]
- CAS No. [63148-62-9] trimethylsiloxy terminated
- Examples 9 and 10 showed that poor print quality was obtained if 3.75% or 5% of X-22-980 was used. This indicated that print quality could be affected on certain printing presses if relatively high levels of X-22-980 were used. It should be noted, however, that Didde Webcom lithographic printing presses were found to successfully print ink containing 5% X-22-980 and that an upper limit for X-22-980 level was dependent on press type.
- Ink did not wet out the inking plate or printing plate very well. Inks were obtained from Kohl & Madden Printing Ink Corp (Minneapolis, MN). Red ink was labeled PMS-185-ABD (OFF-ABD-STD-RED).
- Black Ink was labeled MSP-42200-D-STG-S (OFF-SOY-ABDT-BLACK).
- Comparative examples C100-C101 were carried out in a similar fashion as examples C1-C3.
- the high peel adhesion value in CIO 1 illustrated the detrimental PSA ink interactions that resulted when printing a typical UV-curable lithographic ink onto a paper coated with a release coating.
- low ink transfer and low adhesive contamination were observed when using UV-curable inks and proper curing conditions.
- Comparative Examples C103-C109 Comparative examples C107-C109 (Table 2) showed that typical ink additives, such as polyethylene and polytetrofluoroethylene (such as Telfon®) waxes did not improve release. Comparative examples C103-C106 showed that fluorine-containing monomers and polyethylene glycol monomethacrylate were also ineffective at reducing PSA/ink interactions. JM410-9, 410-8, and 413-3 are typical waxes that are used in lithographic inks.
- JM410-9 is commercially available as "Super Poly 4" from Lawter International, pleasant, WI. JM410-8 is commercially available as "CC5510-D” from Carrol Scientific, Countryside, IL. JM413-3 is commercially available as "PROTECH 200" from Carrol Scientific. Countryside, LL. FluoradTM FX- 13 , FluoradTM FX- 189 and FluoradTM FX- 14 were obtained from 3M Company (Industrial Chemical Products Division, St. Paul, MN).
- CW-750 is polyethylene glycol monomethacrylate 10 moles, EO obtained from Polysciences, Inc., Warrington, PA (Cat. #16713).
- Comparative Examples C110 and Clll Comparative examples C 110 and Cl l l show that the use of mercaptan-free polydimethylsiloxanes that do not have the mercaptan functionality do not provide improved properties.
- polydimethylsiloxane trimethylsiloxy terminated, CAS No. [63148-62-9]
- peel adhesion values for Examples 100-108 show that X-22-980 reduces PSA / ink interactions. Peel adhesion decreases as X-22-980 levels are increased from 1 to 6 wt%. The high re-adhesion values indicate that adhesive contamination is low. Examples 109 and 110 show that poor print quality is obtained if 7.5% or 10% X-
- Examples 109-116 (Table 2) illustrate the positive affects of additives with various amounts of mercapto content and variations in polymer structure. Except for PS 927 and
- PS405 the additives are dimethylsiloxy / 3-mercaptopropylmethylsiloxy copolymers of varying comonomer ratios and molecular weights.
- PS927 is the homopolymer based on a 3-mercaptopropylmethylsiloxy repeat unit.
- PS405 is described as "polydimethylsiloxane, mercaptopropyl t-structure with branch points" by Huls America.
- the additives are described in detail in Table 3.
- Example 117 illustrated that methacrylate-terminated poly(dimethylsiloxane) of a number average molecular weight of 10,000 (Silicone PLUS HG-10, commercially available from 3M) was an effective additive.
- Inks used in these examples were obtained from Zeller Interchem Corporation. Black ink was labeled UVALUX US4826LD; yellow ink was labeled UVALUX US4825LD. Ink additive "X-22-980" was added to the inks at 1, 3 and 5 weight percent based on the weight of the ink. Black ink was cured with 4 lights whereas the yellow ink was cured with one UV light.
- Examples C200-C203 and 201-202 demonstrate that the additives described in this invention can be used to make printed tapes that have good release characteristics.
- Printing was carried out on the non-adhesive side of several strips of 1" (2.54 cm) wide ScotchTM MagicTM Tape (810 tape, commercially available from 3M company, St. Paul, MN) in a similar manner as C 1 and C 100.
- the several strips of ScotchTM MagicTM Tape were laminated next to each other onto bond paper prior to printing in order to create a large area for printing.
- Results in Table 5 show that addition of 2.5% of X-22-980 results in low ink transfer and low peel adhesion for both UV and air-curable inks.
- UV-curable ink UVALUX US423185 LD UN RED obtained from Zeller and
- Air-curable ink PMS-185-ABD (OFF-ABD-STD-RED) obtained from Kohl and Madden Corp.
- Examples C210-C213 and 211-212 demonstrate that the additives described in this invention can be used to make printed labels that have good release characteristics.
- UV-curable ink UVALUX US423185 LD UN RED obtained from Zeller and Gmelin.
- Air-curable ink PMS- 185-ABD (OFF-ABD-STD-RED) obtained from Kohl and Madden Corp.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US111811 | 1987-10-21 | ||
| US11181198A | 1998-07-08 | 1998-07-08 | |
| PCT/US1999/005309 WO2000002966A1 (en) | 1998-07-08 | 1999-03-11 | Additives for printing inks that provide release |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP1102819A1 true EP1102819A1 (en) | 2001-05-30 |
Family
ID=22340570
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP99911311A Withdrawn EP1102819A1 (en) | 1998-07-08 | 1999-03-11 | Additives for printing inks that provide release |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP1102819A1 (https=) |
| JP (1) | JP2002520440A (https=) |
| KR (1) | KR20010053416A (https=) |
| AU (1) | AU749524B2 (https=) |
| CA (1) | CA2336856A1 (https=) |
| WO (1) | WO2000002966A1 (https=) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19905820A1 (de) * | 1998-10-27 | 2000-05-04 | Degussa | Schwefelfunktionelle Polyorganosilane |
| US9353294B2 (en) | 2004-12-14 | 2016-05-31 | 3M Innovative Properties Company | Microstructured release liners |
| KR101850170B1 (ko) | 2010-11-24 | 2018-04-18 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 얇은 코팅 층을 도포하기 위한 이송 코팅의 사용 |
| US10723894B2 (en) | 2014-12-23 | 2020-07-28 | 3M Innovative Properties Company | Tie layers prepared from particle-containing waterborne suspensions |
| US11286404B2 (en) | 2014-12-23 | 2022-03-29 | 3M Innovative Properties Company | Dual-sided multi-layer adhesive |
| FI128373B (en) | 2017-06-20 | 2020-04-15 | Valmet Automation Oy | Method for controlling a recovery boiler |
| WO2021099997A1 (en) | 2019-11-20 | 2021-05-27 | 3M Innovative Properties Company | Medical tapes with high optical clarity when over-taped |
| EP4084956B1 (en) | 2019-12-31 | 2024-12-04 | 3M Innovative Properties Company | Multilayer articles via wet-on-wet processing |
| JP2023520808A (ja) | 2020-04-13 | 2023-05-19 | スリーエム イノベイティブ プロパティズ カンパニー | 有効弾性係数が小さい医療用接着剤物品 |
| EP4262655B1 (en) | 2020-12-21 | 2025-12-10 | Solventum Intellectual Properties Company | Dual-sided adhesive tapes with on-demand adhesion |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS56118472A (en) * | 1980-02-23 | 1981-09-17 | Touka Shikiso Kagaku Kogyo Kk | Ultraviolet-curable ink composition |
| US4589920A (en) * | 1982-10-08 | 1986-05-20 | Mitsubishi Paper Mills, Ltd. | Ink composition utilized in lithographic printing and a lithographic printing process |
| US4596720A (en) * | 1985-10-03 | 1986-06-24 | Dow Corning Corporation | Radiation-curable organopolysiloxane coating composition |
| JPS62197453A (ja) * | 1986-02-25 | 1987-09-01 | Shin Etsu Chem Co Ltd | シリコ−ン組成物 |
| JP2919732B2 (ja) * | 1993-12-03 | 1999-07-19 | 大日精化工業株式会社 | 剥離性処理剤 |
| JPH107969A (ja) * | 1996-06-21 | 1998-01-13 | Showa Denko Kk | インク組成物 |
| JPH107958A (ja) * | 1996-06-25 | 1998-01-13 | Showa Denko Kk | 水性インク用添加剤および水性インク組成物 |
| JPH1088055A (ja) * | 1996-09-18 | 1998-04-07 | Sumitomo Rubber Ind Ltd | オフセット印刷用インキおよびそれを用いたカラーフィルタの製造方法 |
-
1999
- 1999-03-11 AU AU29984/99A patent/AU749524B2/en not_active Ceased
- 1999-03-11 WO PCT/US1999/005309 patent/WO2000002966A1/en not_active Ceased
- 1999-03-11 KR KR1020017000202A patent/KR20010053416A/ko not_active Withdrawn
- 1999-03-11 EP EP99911311A patent/EP1102819A1/en not_active Withdrawn
- 1999-03-11 JP JP2000559192A patent/JP2002520440A/ja active Pending
- 1999-03-11 CA CA002336856A patent/CA2336856A1/en not_active Abandoned
Non-Patent Citations (1)
| Title |
|---|
| See references of WO0002966A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| AU749524B2 (en) | 2002-06-27 |
| AU2998499A (en) | 2000-02-01 |
| KR20010053416A (ko) | 2001-06-25 |
| WO2000002966A1 (en) | 2000-01-20 |
| JP2002520440A (ja) | 2002-07-09 |
| CA2336856A1 (en) | 2000-01-20 |
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