GB2311787A - Printing Ink - Google Patents
Printing Ink Download PDFInfo
- Publication number
- GB2311787A GB2311787A GB9706404A GB9706404A GB2311787A GB 2311787 A GB2311787 A GB 2311787A GB 9706404 A GB9706404 A GB 9706404A GB 9706404 A GB9706404 A GB 9706404A GB 2311787 A GB2311787 A GB 2311787A
- Authority
- GB
- United Kingdom
- Prior art keywords
- water
- monomer
- ink
- resin
- curable ink
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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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
- C09D11/10—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
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
A water-based, UV-curable ink for plastic substrates, comprising: a) a water-dispersible or water-soluble urethane acrylate oligomer; b) a monomer eg hexane diol diacrylate that is capable of softening the substrate in part or in full; the monomer being resistant to hydrolysis; and c) a passive resin that is soluble in the monomer. Resin (c) may be poly(meth)acrylate, polyester or epoxy, vinyl, ketone, phenoxy or cellulosic resin.
Description
PRINTING INK
The present invention concerns a printing ink, and in particular a water-based,
UV-curable printing ink that is capable of adhering to plastic substrates.
A typical water-based, UV-curable ink currently on the market comprises: a non-ionic water soluble urethane acrylate; monomers such as tripropylene glycol diacrylate ('TPGDA') and ethoxylated trimethylol propane triacrylate ('ETMPTA'); water; a thickener; photoinitiators; flow aids; and pigments. The ink can be printed on to paper and board substrates through a plain weave mesh having a 150/cm mesh count. The inks exhibit good adhesion to paper and board substrates. Adhesion to substrates can be tested by scratching the dried ink with a fingernail and observing whether any ink is removed. If the ink is printed on to plastic substrates such as PVC or polystyrene, the adhesion is very poor and the ink can be easily removed by scratching.
The present invention is concerned with the problem of providing a water-based,
UV-curable printing ink that exhibits improved adhesion to plastic substrates such as PVC and polystyrene.
In accordance with the present invention there is provided a water-based,
UV-curable ink that is capable of adhering to a plastic substrate, comprising:
a) a water-dispersible or water-soluble urethane acrylate oligomer;
b) a monomer that is capable of softening the substrate in part or in full; the monomer being resistant to hydrolysis; and
c) a passive resin that is soluble in the monomer.
In accordance with the present invention there is provided a method for preparing a water-based, UV-curable ink that is capable of adhering to a plastic substrate, the method comprising the steps of: a) selecting a monomer that is capable of softening the plastic substrate in part or in full and is resistant to hydrolysis; b) selecting a passive resin that is soluble in the monomer; c) dissolving the passive resin in the monomer; d) blending the passive resin and the monomer with a water-dispersible or water-soluble urethane acrylate oligomer; and e) adding water to the blend.
The water-based, UV-curable ink preferably comprises:
a) from 3 to 30 %, preferably from 10 to 20 %, by weight of the water-dispersible or water-soluble urethane acrylate oligomer;
b) from 10 to 50 %, preferably from 25 to 35 %, by weight of the monomer that is capable of softening the substrate in part or in full and is resistant to hydrolysis; and
c) from 1 to 25 %, preferably from 5 to 15 %, by weight of the passive resin that is soluble in the monomer.
By the term 'passive resin' we mean a resin that would not substantially take part in a free radicle, photopolymerisation reaction.
The inventors of the present invention have found a water-based, UV-curable ink that exhibits adhesion to plastic substrates such as polystyrene and PVC.
The monomer is preferably hexane diol diacrylate ('HDDA'). HDDA is a difunctional acrylate that offers a high cure rate. HDDA also exhibits excellent compatibility with and solvency for other resins and additives used in the ink.
The passive resin is preferably selected from the following list: solid epoxies, ketone resins, acrylate and methacrylate copolymers, vinyl resins, solid polyesters, phenoxy resins and cellulosics. The most preferred passive resins are acrylate or methacrylate copolymers.
The resin preferably has a Tg between 30 and 1300C.
Preferably at least 25 parts by weight of resin are dissolved in the monomer.
The ink preferably comprises at least 10%, more preferably at least 18%, even more preferably at least 25%, of water, based on the total weight of the ink.
The passive resin is preferably present in the ink in an amount from 1-25%, more preferably from 5-15%, by total weight.
The ink is preferably prepared by dissolving the selected passive resin in the monomer, and then adding the other components of the ink to the dissolved resin. A normal mechanical stirrer is used to disperse the components. A special high shear mixer is not required.
The ink can include any of the usual additives that are present such as: pigments, surfactants, UV stabilisers, photoinitiators and synergists, waxes, rheology modifiers, and other commonly used monomers and oligomers.
Examples
Tests to Find a Suitable Monomer
Test for Monomer's Ability to Soften a Plastic Substrate
In order to test whether any of the selection of monomers iisted below are capable of softening plastic substrates such as polystyrene and self-adhesive
PVC, a small drop of each of the monomers was placed on to polystyrene and
PVC substrates. After being left for 5 minutes, the monomers were removed from the substrates using a soft cloth and the surface of the substrates was examined for softening and marking. The results are as follows:
Monomer Polystyrene Self-Adhesive PVC
(Mactac 8129)
Tripropyleneglycol diacrylate no mark no mark
Ethoxylated trimethylol propane no mark no mark triacrylate
Trimethyl propane triacrylate no mark no mark
substrate softened 2 phenoxyethyl acrylate no mark no mark
Di-propylene glycol diacrylate no mark substrate softened
N vinyl caprolactam* substrate softened substrate softened
N N di-vinyl imidazole* substrate softened substrate softened
N vinyl pyrolidone substrate softened substrate softened
Hexane diol diacrylate substrate softened substrate softened
N vinyl formamide substrate softened substrate softened
Neopentyl glycol diacrylate no mark no mark
Octyldecyl acrylate no mark substrate softened * 30% solutions in TPGDA since they are solid at ambient temperature.
The results show that only five out of the twelve monomers that were tested were capable of softening both plastic substrates.
Test For Monomer's Hydrolysis Resistance:
In order for the monomer to be used in a water-based ink, it needs to be resistant to hydrolysis. The five monomers that were capable of softening the polyolefin were tested for their resistance to hydrolysis. The monomers were tested for their hydrolytic stability under both acidic and basic conditions. Ten percent dispersions of the monomers were prepared in deionised water, with the pH being adjusted to 5 and 9 with dilute HCI and NaOH respectively. The samples were stored for 1 week at 40 OC and then checked for degradation using HPLC.
Of the monomers tested, hexane diol diacrylate (HDDA) gave the best resistance properties.
Test for Monomer's Compatibility with other Components in the Ink:
The monomer's compatibility with other components in the ink was tested by formulating the ink and checking for general problems such as separation on storage. The test was carried out using HDDA and the HDDA was found to be compatible with the ink's other components.
Tests to find a Suitable Passive Resin
Test for Solubility in Monomer:
In the inks of the present invention, the passive resin must be soluble in the monomer. To test whether a selection of resins were soluble in HDDA, 25% solids solutions of a range of passive resin types were prepared in HDDA and the solutions were examined for clarity and stability towards separation. The solubility is largely linked to molecular weight within a group of similar resins: the lower molecular weight examples have the best solubility.
The test revealed that the following passive resins are suitable for incorporation into the inks of the present invention: solid epoxies, ketone resins, acrylate and methacrylate copolymers, vinyl resins, solid polyesters, phenoxy resins and cellulosics. The most preferred passive resins are acrylate or methacrylate copolymers.
Adhesion Test:
A selection of passive resins were incorporated into inks, and the inks were tested for their adhesion to a polystyrene substrate. The inks were made by initially preparing a 25% solids solution of the resin in HDDA. The other components of the ink were added sequentially while stirring with a mechanical stirrer. A formula similar to Example 1 below was used.
The inks were screen printed through a 150 plain weave mesh on to a polystyrene substrate. The films were cured at 30 m/min using 2 lamps at full power (Svecia UV drier, 2 80w/cm medium mercury lamps). After the films were dried, they were examined for adhesion by scratching the films with a finger nail and observing whether the film was damaged or removed. The results are as follows:
Resin Type Result
Paraloid B66 Methacrylate copolymer Excellent film that could (sold by CHEMAC) not be removed by
scratching
Plexigum M345 Methacrylate copolymer Excellent film that could (sold by Huls) not be removed by
scratching
Adhesion resin LTH Polyester Good film that could only (sold by Huls) be removed with difficulty
by scratching
Synthetic resin 8K Ketone Fair adhesion but film (sold by Huls) could be removed by
scratching
Surcol 836 Methacrylate copolymer Good film that could only (sold by Allied Colloids be removed with difficulty
Limited) by scratching
CAB 381 Cellulosic Poor film that could easily (sold by EGGAR) be removed
Epikote 1001 Epoxy Poor film that could easily (sold by SHELL) be removed
Paphen-phenoxy Phenoxy Good film that could
PKHH only be removed with (sold by Phenoxy difficulty by scratching
Associates)
As can be seen from the results in the above table, the best results were given by acrylate and methacrylate copolymers, phenoxy resins and solid polyester resins. The methacrylate copolymers exhibited the best combination of results for adhesion, solubility in the monomer and hydrolytic solubility. Further tests showed that hard, high Tg polymers exhibited the best adhesion results.
Hydrolytic Stability:
Resins were not tested for their hydrolytic stability in isolation. No particular problems were encountered with hydrolytic stability of the resins used in the previous tests. Methacrylate copolymers were selected on the basis that their other properties were suitable and that they are well known for their hydrolytic stability. Experimental ink samples were however checked for changes in pH on storage. A decrease in pH indicates hydrolysis problems.
Determination of Water Content
The following test was used to determine the required water content for the ink:
A range of experimental inks were prepared with a water content ranging from 10% to 45%. The viscosities were adjusted using HDDA so that all of the inks were identical. The inks were printed through 150 plain weave mesh on to 500 micron polystyrene substrate. The films were cured with 1 pass through a Svecia
UV drier at 25 m/min (2x 80w/cm medium pressure mercury lamps). The films were compared for their hardness and adhesion by scratching the films with a fingernail. The maximum water level giving acceptable adhesion was determined. A level of approximately 25% was found to give excellent adhesion and an excellent film weight. Higher levels of water can be used but problems with water retention in the film occur and a predry stage may be required before
UV curing.
Preparation and Testing of Inks
The following inks were prepared:
Example 1
Plexigum M3451 6.0
Hexane diol diacrylate 28.3
Surfactant 1.0
Water soluble urethane acrylate oligomer 12.6
Water 25.0
Isopropyl thioxanthone 0.49
Irgacure 184 2.93
Amine synergist 1.98
Di trimethylol propane tetra acrylate 8.0
Magenta pigment base 2 13.0
UV stabiliser 0.7
Total 100.0 'Available from Huls
Example 2
Paraloid B663 6.0
Hexane diol diacrylate 28.3
Surfactant 1.0
Water soluble urethane acrylate oligomer 12.6
Water 25.0
Isopropyl thioxanthone 0.49
Irgacure 184 2.93
Amine synergist 1.98
Di trimethylol propane tetra acrylate 8.0
Magenta pigment base 2 13.0
UV stabiliser 0.7
Total 100.0 3 Available from CHEMAC 2 Magenta pigment base.
Polyester urethane acrylate 37.64
Tripropylene glycol diacrylate 37.09
UV stabiliser 0.18
Sunfast magenta 228 0013 19.64
Cromophthal red BRN 5.45
Comparative Example 1
Water soluble urethane acrylate oligomer 35.0
Tripropylene glycol diacrylate 14.0
Irgacure 184 2.0
Silicone flow aid 1.0
Surfactant 1.0
Magenta pigment 2.5
Water 43.5
UV stabiliser 1.0
Total 100.0
Comparative Example 2
Water soluble urethane acrylate oligomer 35.0
Hexane diol diacrylate 14.0
Irgacure 184 2.0
Silicone flow aid 1.0
Surfactant 1.0
Magenta pigment 2.5
Water 43.5
UV stabiliser 1.0
Total 100.0
Comparative Example 3
Plexigum M345 6.0
N-vinyl caprolactam 18.3
Ethoxylated trimethylol propane triacrylate 10.0
Surfactant 1.0
Water soluble urethane acrylate 12.6
Water 25.0
Isopropyl thioxanthone 0.49
Irgacure 184 2.93
Amine synergist 1.98
Di trimethylol propane tetra acrylate 8.0
Magenta pigment base2 13.0
UV stabiliser 0.7
Total 100.0
The inks were printed as before using a 150 plain weave mesh and a selection of substrates. The films were dried using a Svecia UV drier ( 2 x 80w/cm mercury lamps).
The inks were tested for their adhesion to plastic substrates using the following methods: a) fingernail scratch test as previously described; and b) cross hatch tape adhesion: The films were scored using a scalpel so that a block of one hundred 1 mum squares were produced. A small piece of adhesive tape was fixed securely over the scored area and removed with a swift wrist action. The adhesion is gauged by the number of small squares removed from the substrate.
Results
Ink Adhesion to Plastic Substrates Example 1 Excellent adhesion to plastic substrates including self-adhesive PVC, rigid PVC and polystyrene Example 2 Excellent adhesion to plastic substrates including self-adhesive PVC, rigid PVC and polystyrene Comparative Example 1 Extremely poor adhesion to plastic substrates Comparative Example 2 Exhibited only limited adhesion to some plastic substrates such as self-adhesive PVC Comparative Example 3 Exhibited excellent adhesion to plastic substrates such as self-adhesive PVC, rigid PVC and polystyrene; however, ageing of the wet ink at 40 OC for 4 weeks caused the ink to exhibit poor adhesion because of poor hydrolysis resistance.
The above results clearly show that only inks falling within the present invention exhibit good adhesion to plastic substrates such as self-adhesive PVC, rigid PVC and polystyrene.
Claims (8)
1. A water-based, UV-curable ink for plastic substrates, comprising:
a) a water-dispersible or water-soluble urethane acrylate oligomer;
b) a monomer that is capable of softening the substrate in part or in full; the monomer being resistant to hydrolysis; and
c) a passive resin that is soluble in the monomer.
2. The water-based, UV-curable ink as claimed in claim 1, wherein the monomer is hexane diol diacrylate.
3. The water-based, UV-curable ink as claimed in claims 1 or 2, wherein the passive resin is selected from the following list: solid epoxies, ketone resins, acrylate and methacrylate copolymers, vinyl resins, solid polyesters, phenoxy resins and cellulosics; the passive resin preferably being an acrylate or methacrylate copolymer.
4. The water-based, UV-curable ink as claimed in claims 1, 2 or 3, wherein at least 25 parts by weight of passive resin are dissolved in the monomer.
5. The water-based, UV-curable ink as claimed in claims 1, 2, 3 or 4, wherein the ink comprises at least 10%, preferably at least 18%, more preferably at least 25%, of water, based on the total weight of the ink.
6. The water-based, UV-curable ink as claimed in any one of the preceding claims, wherein the passive resin has a Tg between 30 and 1300C.
7. The water-based, UV-curable ink as claimed in any one of the preceding claims, wherein the passive resin is present in the ink in an amount from 1-25%, preferably from 5-15%, by total weight.
8. A method for preparing a water-based, UV-curable ink that is capable of adhering to plastic substrates, the method comprising the steps of: a) selecting a monomer that is capable of softening the plastic substrate in part or in full and is resistant to hydrolysis; b) selecting a passive resin that is soluble in the monomer; c) dissolving the passive resin in the monomer; d) blending the passive resin and the monomer with a water-dispersible or water-soluble urethane acrylate oligomer; and e) adding water to the blend.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9706404A GB2311787B (en) | 1996-04-02 | 1997-03-27 | A printing ink |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9606966.1A GB9606966D0 (en) | 1996-04-02 | 1996-04-02 | Printing ink |
| GB9706404A GB2311787B (en) | 1996-04-02 | 1997-03-27 | A printing ink |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| GB9706404D0 GB9706404D0 (en) | 1997-05-14 |
| GB2311787A true GB2311787A (en) | 1997-10-08 |
| GB2311787B GB2311787B (en) | 2000-04-05 |
Family
ID=26309049
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB9706404A Expired - Fee Related GB2311787B (en) | 1996-04-02 | 1997-03-27 | A printing ink |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB2311787B (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2314851B (en) * | 1996-07-02 | 2000-03-15 | Sericol Ltd | An ink jet ink |
| GB2357514A (en) * | 1999-12-23 | 2001-06-27 | Sericol Ltd | An ink for decoration of paper substrates for poster displays |
| EP1260563A1 (en) * | 2001-05-21 | 2002-11-27 | Sicpa Holding S.A. | UV curing intaglio ink |
| EP1829941A1 (en) * | 2006-03-03 | 2007-09-05 | FUJIFILM Corporation | Ink composition, inkjet recording method, process for producing lithographic printing plate, and lithographic printing plate |
| EP1903080A1 (en) * | 2006-09-22 | 2008-03-26 | FUJIFILM Corporation | Ink composition, inkjet recording method, and printed material |
| US8975307B2 (en) | 2009-06-25 | 2015-03-10 | Sericol Limited | Printing method |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2008139A (en) * | 1977-11-03 | 1979-05-31 | Somar Mfg | Radiation curable resin composition |
| US4271258A (en) * | 1980-06-11 | 1981-06-02 | Tamura Kaken Co., Ltd. | Photopolymerizable ink compositions |
| JPS57108106A (en) * | 1980-12-24 | 1982-07-06 | Mitsubishi Rayon Co Ltd | Curing by ultraviolet ray irradiation |
| EP0125710A2 (en) * | 1983-04-11 | 1984-11-21 | International Standard Electric Corporation | U.V. curable coating for optical fibers |
| EP0311288A2 (en) * | 1987-09-30 | 1989-04-12 | Westinghouse Electric Corporation | Improvements in or relating to resin compositions curable with ultraviolet light |
| GB2256874A (en) * | 1991-06-07 | 1992-12-23 | Sericol Ltd | Photocurable compositions |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1995028436A1 (en) * | 1994-04-19 | 1995-10-26 | Lehigh University | Printing ink compositions, methods for making same and uses thereof |
-
1997
- 1997-03-27 GB GB9706404A patent/GB2311787B/en not_active Expired - Fee Related
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2008139A (en) * | 1977-11-03 | 1979-05-31 | Somar Mfg | Radiation curable resin composition |
| US4271258A (en) * | 1980-06-11 | 1981-06-02 | Tamura Kaken Co., Ltd. | Photopolymerizable ink compositions |
| JPS57108106A (en) * | 1980-12-24 | 1982-07-06 | Mitsubishi Rayon Co Ltd | Curing by ultraviolet ray irradiation |
| EP0125710A2 (en) * | 1983-04-11 | 1984-11-21 | International Standard Electric Corporation | U.V. curable coating for optical fibers |
| EP0311288A2 (en) * | 1987-09-30 | 1989-04-12 | Westinghouse Electric Corporation | Improvements in or relating to resin compositions curable with ultraviolet light |
| GB2256874A (en) * | 1991-06-07 | 1992-12-23 | Sericol Ltd | Photocurable compositions |
Non-Patent Citations (1)
| Title |
|---|
| WPI Abstract Accession No. 82-67161E & JP 57 108 106 A * |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2314851B (en) * | 1996-07-02 | 2000-03-15 | Sericol Ltd | An ink jet ink |
| GB2357514A (en) * | 1999-12-23 | 2001-06-27 | Sericol Ltd | An ink for decoration of paper substrates for poster displays |
| EP1260563A1 (en) * | 2001-05-21 | 2002-11-27 | Sicpa Holding S.A. | UV curing intaglio ink |
| WO2002094952A1 (en) * | 2001-05-21 | 2002-11-28 | Sicpa Holding S.A. | Uv curing intaglio ink |
| US6787583B2 (en) | 2001-05-21 | 2004-09-07 | Sicpa Holding S.A. | UV curing intaglio ink |
| AU2002338930B2 (en) * | 2001-05-21 | 2008-05-01 | Sicpa Holding Sa | UV curing intaglio ink |
| KR100852648B1 (en) | 2001-05-21 | 2008-08-18 | 시크파 홀딩 에스.에이. | Uv curing intaglio ink |
| EP1829941A1 (en) * | 2006-03-03 | 2007-09-05 | FUJIFILM Corporation | Ink composition, inkjet recording method, process for producing lithographic printing plate, and lithographic printing plate |
| US7935742B2 (en) | 2006-03-03 | 2011-05-03 | Fujifilm Corporation | Ink composition, inkjet recording method, process for producing lithographic printing plate, and lithographic printing plate |
| EP1903080A1 (en) * | 2006-09-22 | 2008-03-26 | FUJIFILM Corporation | Ink composition, inkjet recording method, and printed material |
| US8975307B2 (en) | 2009-06-25 | 2015-03-10 | Sericol Limited | Printing method |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2311787B (en) | 2000-04-05 |
| GB9706404D0 (en) | 1997-05-14 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 20090327 |