CN103666041B - A kind of UV curable ink and preparation method thereof - Google Patents
A kind of UV curable ink and preparation method thereof Download PDFInfo
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- CN103666041B CN103666041B CN201310600481.5A CN201310600481A CN103666041B CN 103666041 B CN103666041 B CN 103666041B CN 201310600481 A CN201310600481 A CN 201310600481A CN 103666041 B CN103666041 B CN 103666041B
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Abstract
The invention discloses a kind of UV curable ink, it is characterized in that, raw material by following weight portion is made: pigment 4-5, UV pure acrylic resin 40-45, trimethylolpropane triacrylate 10-15, ethyl acetate 5-8, methyl methacrylate 12-15, zirconium-n-propylate 3-4, sodium phosphate trimer 5-6, nickel nitrate 1-2, Arabic gum 1-2, butyl acrylate 3-4, dipentaerythritol acrylate 6-9, antioxidant 1035? 2-3, triethyl citrate 3-4, captax 1-2, silane resin acceptor kh-550? 2-3, auxiliary agent 4-5, light trigger 184? 6-12, auxiliary agent of the present invention has improved the toughness of ink, makes distributes ink even, and has maintained the stability of ink, the UV curable ink photocuring time of the present invention is short, does not need heating, saves energy resource consumption, pollution-free to atmosphere, high comprehensive performance.
Description
Technical field
The present invention relates to a kind of ink and preparation method thereof, particularly a kind of UV curable ink and preparation method thereof.
Background technology
Ultraviolet light polymerization (UV) ink refers under ultraviolet ray is irradiated, utilizes the ultraviolet light of different wave length and energy to make ink film forming and dry ink. The curing mechanism of UV curable ink is, the light trigger in system directly or indirectly absorbs after ultraviolet luminous energy, from ground state transition to excited singlet, alters and jump to excited triplet state between being; After excited singlet or triplet state experience unimolecule or bimolecular chemical action, the biologically active fragment that generation can trigger monomer polymerization, these fragments can be free radical, cation, anion or ion free radical. Utilize different ultraviolet spectras, can produce different-energy, the monomer polymerization in different ink vehicles is become to polymer, so the look film of UV ink has good machinery and chemical property. The major advantage of UV ink has: (1) is without solvent; (2) rate of drying is fast, and power consumption is few; (3) good luster, bright in luster; (4) water-fast, resistance to solvent, anti-wear performance is good. In UV ink, light trigger is that one is subject to light activated compound, after absorption illumination, is excited into free radical, and energy is transferred to photonasty molecule or photocrosslinking agent, makes UV China ink that photocuring reaction occur. UV China ink has become a kind of more ripe ink technology at present, and its pollutant emission is almost nil. Except not containing solvent, UV China ink is also just like being difficult for scumming, and site is clear, the bright-coloured light of mass colour, chemical-resistance excellence, the advantage such as low-consuming.
Summary of the invention
The object of this invention is to provide a kind of UV curable ink and preparation method thereof.
In order to realize object of the present invention, the present invention passes through following scheme implementation:
A kind of UV curable ink, is made up of the raw material of following weight portion: pigment 4-5, UV pure acrylic resin 40-45, trimethylolpropane triacrylate 10-15, ethyl acetate 5-8, methyl methacrylate 12-15, zirconium-n-propylate 3-4, sodium phosphate trimer 5-6, nickel nitrate 1-2, Arabic gum 1-2, butyl acrylate 3-4, dipentaerythritol acrylate 6-9, antioxidant 10352-3, triethyl citrate 3-4, captax 1-2, silane resin acceptor kh-550 2-3, auxiliary agent 4-5, light trigger 1846-12;
Described auxiliary agent is prepared from by the raw material of following weight portion: nano diatomite powder 0.2-0.3, nano mica powder 0.2-0.3, silane resin acceptor kh-550 2-3, morpholine 1-2, neopentyl glycol 3-4, antioxidant 10351-2, crosslinking agent TAC2-3, tri (propylene glycol) diacrylate 10-12,1-Methoxy-2-propyl acetate 5-10, n-propyl gallate 2-3, coix seed oil 1-2; Its preparation method is by each mixing of materials, is heated to 60-70 DEG C, and stirring reaction 30-40 minute, to obtain final product.
UV curable ink of the present invention, made by following concrete steps:
First add pigment, UV pure acrylic resin, trimethylolpropane triacrylate, ethyl acetate, methyl methacrylate, zirconium-n-propylate, sodium phosphate trimer to stir and evenly mix, be heated to 80-90 DEG C, stir 25-35 minute; Then add all the other residual components except light trigger 184, stirring reaction 3-5 hour; Finally be cooled to 60-70 DEG C, add light trigger 184, stirring reaction 40-50 minute, cooling after, grind obtain 20-40 μ m slurry, to obtain final product.
Beneficial effect of the present invention: auxiliary agent of the present invention has improved the toughness of ink, makes distributes ink even, and has maintained the stability of ink; The UV curable ink photocuring time of the present invention is short, does not need heating, saves energy resource consumption, pollution-free to atmosphere, high comprehensive performance.
Specific embodiments
Below by instantiation, the present invention is described in detail.
A kind of UV curable ink, by following weight portion (kilogram) raw material make: pigment 4, UV pure acrylic resin 40, trimethylolpropane triacrylate 10, ethyl acetate 5, methyl methacrylate 12, zirconium-n-propylate 3, sodium phosphate trimer 5, nickel nitrate 1, Arabic gum 1, butyl acrylate 3, dipentaerythritol acrylate 6, antioxidant 10352, triethyl citrate 3, captax 1, silane resin acceptor kh-550 2, auxiliary agent 4, light trigger 1846;
Described auxiliary agent by following weight portion (kilogram) raw material be prepared from: nano diatomite powder 0.2, nano mica powder 0.2, silane resin acceptor kh-550 2, morpholine 1, neopentyl glycol 3, antioxidant 10351, crosslinking agent TAC2, tri (propylene glycol) diacrylate 10,1-Methoxy-2-propyl acetate 5, n-propyl gallate 2, coix seed oil 1; Its preparation method is by each mixing of materials, is heated to 60-70 DEG C, and stirring reaction 30-40 minute, to obtain final product.
UV curable ink of the present invention, made by following concrete steps:
First add pigment, UV pure acrylic resin, trimethylolpropane triacrylate, ethyl acetate, methyl methacrylate, zirconium-n-propylate, sodium phosphate trimer to stir and evenly mix, be heated to 80-90 DEG C, stir 25-35 minute; Then add all the other residual components except light trigger 184, stirring reaction 3-5 hour; Finally be cooled to 60-70 DEG C, add light trigger 184, stirring reaction 40-50 minute, cooling after, grind obtain 20-40 μ m slurry, to obtain final product.
The ink of gained, uses cross-hatching ox-hide tape stripping, draws compartment apart from 1mm, and 100% adheres to; Spirituous cotton balls is soaked in use, and 300 grams of pressure wipings 50 times, are as good as shape; Be soaked in salad oil (normal temperature) 8 hours, be as good as shape; Use is soaked with the cotton balls of salt solution, and 300 grams of pressure wipings 50 times, are as good as shape.
Claims (2)
1. a UV curable ink, it is characterized in that, be prepared from by the raw material of following weight portion: pigment 4-5, UV pure acrylic resin 40-45, trimethylolpropane triacrylate 10-15, ethyl acetate 5-8, methyl methacrylate 12-15, zirconium-n-propylate 3-4, sodium phosphate trimer 5-6, nickel nitrate 1-2, Arabic gum 1-2, butyl acrylate 3-4, dipentaerythritol acrylate 6-9, antioxidant 10352-3, triethyl citrate 3-4, captax 1-2, silane resin acceptor kh-550 2-3, auxiliary agent 4-5, light trigger 1846-12;
Described auxiliary agent is prepared from by the raw material of following weight portion: nano diatomite powder 0.2-0.3, nano mica powder 0.2-0.3, silane resin acceptor kh-550 2-3, morpholine 1-2, neopentyl glycol 3-4, antioxidant 10351-2, crosslinking agent TAC2-3, tri (propylene glycol) diacrylate 10-12,1-Methoxy-2-propyl acetate 5-10, n-propyl gallate 2-3, coix seed oil 1-2; Its preparation method is by each mixing of materials, is heated to 60-70 DEG C, and stirring reaction 30-40 minute, to obtain final product.
2. UV curable ink according to claim 1, is characterized in that, is made up of following concrete steps:
First add pigment, UV pure acrylic resin, trimethylolpropane triacrylate, ethyl acetate, methyl methacrylate, zirconium-n-propylate, sodium phosphate trimer to stir and evenly mix, be heated to 80-90 DEG C, stir 25-35 minute; Then add all the other residual components except light trigger 184, stirring reaction 3-5 hour; Finally be cooled to 60-70 DEG C, add light trigger 184, stirring reaction 40-50 minute, cooling after, grind obtain 20-40 μ m slurry, to obtain final product.
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CN201310600481.5A CN103666041B (en) | 2013-11-25 | 2013-11-25 | A kind of UV curable ink and preparation method thereof |
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CN201310600481.5A CN103666041B (en) | 2013-11-25 | 2013-11-25 | A kind of UV curable ink and preparation method thereof |
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CN103666041A CN103666041A (en) | 2014-03-26 |
CN103666041B true CN103666041B (en) | 2016-05-04 |
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CN103923526B (en) * | 2014-04-30 | 2016-02-24 | 苏州安洁科技股份有限公司 | Semi-transparent grey environment-friendly ink |
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IL103705A (en) * | 1991-11-15 | 1995-12-08 | Kuehnle Manfred R | Electrothermal printing ink and method and apparatus for electronic printing therewith |
CN1552778B (en) * | 2003-06-06 | 2010-04-28 | 深圳市海川实业股份有限公司 | Ultraviolet photocurable anti-static printing ink |
CN101870834B (en) * | 2010-06-18 | 2013-06-19 | 北京赛腾工业标识系统有限公司 | Code-spraying printing ink |
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Effective date of registration: 20230323 Address after: No. 259, Mount Taishan Road, National Economic and Technological Development Zone, Hebi, Henan 458030 Patentee after: HEBI RUITELONG BIOMASS MATERIALS TECHNOLOGY Co.,Ltd. Address before: 244000 No. 3201, Cuihu Fourth Road, Tongling Economic Development Zone, Anhui Province Patentee before: TONGLING FOUNDER PLASTICS TECHNOLOGY Co.,Ltd. |