CN103865325A - Preparation method of green golden printing ink - Google Patents
Preparation method of green golden printing ink Download PDFInfo
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- CN103865325A CN103865325A CN201410121559.XA CN201410121559A CN103865325A CN 103865325 A CN103865325 A CN 103865325A CN 201410121559 A CN201410121559 A CN 201410121559A CN 103865325 A CN103865325 A CN 103865325A
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Abstract
The invention discloses a preparation method of green golden printing ink. The preparation method is realized through the following technical scheme: preparing a mixed solvent by using butanone and n-propyl propionate; then, dissolving 5 parts of green-light gold into 11-13 parts of mixed solvent; next, sequentially adding 20 parts of varnish, 4 parts of 407 yellow and 1 part of 105 primary red into the mixed solvent, and sufficiently and uniformly stirring all the components. As an optimization, the preparation method has the advantages that the stirring temperature ranges from 40 DEG C to 60 DEG C, the weight ratio of butanone to n-propyl propionate in the mixed solvent is 1:1, varnish is 25-60% of acrylic acid gold varnish, cadmium sulfide is used as the main component of 407 yellow, ferric oxide is used as the main component of 105 primary red, the mesh number of green-light gold is 1200, the surface area of particles of 407 yellow is larger than 50m<2>/g, and the surface area of particles of 105 primary red is larger than 60m<2>/g. The preparation method is simple in preparation process, and the standard color characteristics including color infiltration intensity and color intensity are kept in the use process of the printing ink.
Description
Technical field
The present invention relates to a kind of ink preparation field, be specially a kind of making method of blue or green gold ink.
Background technology
At present, people have not only been confined to its aesthetic property to the pursuit of commodity outer packaging, but more and more pay attention to safety performance and the environmental-protecting performance of its packing, in order to strengthen image product, increase antifalse effect, adopt gravure techniques printing on packing film.Ink is the important materials for wrapping material printing, and it comprises main component and ancillary component by printing by pattern, the present stock curing ink of literal table, and they mix equably and form the gluey fluid of a kind of viscosity through repeat-rolling.Formed by pigment, low-melting ink vehicle and auxiliary agent and solvent etc.
Wherein, pigment is exactly to make object catch the material of color.Pigment have a solubility with insolubility, have inorganic and organically difference.Mineral dye is generally mineral material, and the mankind know use mineral dye very early, utilizes coloured soil and ore, draws a picture and smear health on crag.Pigment dyestuff is generally taken from plant and marine animal, the purple refining from shellfish as alizarin blue, gamboge and ancient Roman.
Pigment divides from chemical constitution, can be divided into mineral dye and the large class of pigment dyestuff two, can be divided into again natural pigment and synthetic dyestuff with regard to its source.Natural pigment is take mineral as source, as: cinnabar, laterite, realgar, Victoria Green WPB and water-ground limestone coloured drawing pigment wollastonite among the people, ground barium sulfate, talcum powder, mica powder, kaolin etc.Take biology as source, Tathagata is from animal: cochineal, natural pearl white etc.; From having of plant: gamboge, sodium alizarinsulfonate, indigo-blue etc.Synthetic dyestuff is by synthetic, as mineral dyes such as titanium white, lithopone, lead-chrome yellow, barba hispanicas, and the pigment dyestuff such as red, even yellowish, phthalocyanine blue, quinacridone.Classify with the function of pigment as rust-stabilising pigment, magnetic paint, luminous pigment, pearly pigment, conducting pigment etc.With color classification, it is method convenient and that use.So pigment can be divided into white, yellow, redness, blueness, green, brown, purple, black, and ignores its source or chemical constitution.
Summary of the invention
The object of the invention is in order to provide a kind of in ink uses, the chromatic characteristic that can maintain the standard enters the making method of the blue or green gold ink of colour strength and tinctorial strength.
For solving the problems of the technologies described above, the present invention adopts following technical scheme to realize:
Butanone and n-propyl are made to mixed solvent, then get 5 parts of green light gold, be dissolved in 11～13 parts of mixed solvents, then to add successively in mixed solvent 20 parts of stand linseed oil, 4 part 407 yellow and 1 part 105 former red, it is fully stirred evenly.
As optimization, the temperature wherein stirring is 40～60 ℃, in mixed solvent, the weight ratio of butanone and n-propyl is 1:1, stand linseed oil is the vinylformic acid blending oil of 25-60%, the main component of 407 Huangs is Cadmium Sulfide, and 105 former red main components are ferric oxide, and green light gold adopts 1200 orders, long-pending 50 meters squared per gram that are greater than of particle surface of 407 Huangs, long-pending 60 meters squared per gram that are greater than of 105 former red particle surfaces.
Green light bronze ink of the present invention is formed by green light gold, stand linseed oil, 407 Huangs, the 105 former raw material produced with combination such as red, and preparation technology is simple, in ink uses, has kept the chromatic characteristic of standard to enter colour strength and tinctorial strength.
Embodiment
The invention will be further described for embodiment plan given below; but can not be interpreted as it is limiting the scope of the invention; according to the present invention, content, to nonessential improvement and adjustment more of the present invention, still belongs to protection scope of the present invention to those skilled in the art.
Embodiment 1
Butanone and n-propyl are made to mixed solvent, then get 5 parts of green light gold, be dissolved in 11 parts of mixed solvents, then to add successively in mixed solvent 20 parts of stand linseed oil, 4 part 407 yellow and 1 part 105 former red, it is fully stirred evenly.The temperature wherein stirring is 40 ℃, in mixed solvent, the weight ratio of butanone and n-propyl is 1:1, stand linseed oil is 30% vinylformic acid blending oil, the main component of 407 Huangs is Cadmium Sulfide, 105 former red main components are ferric oxide, green light gold adopts 1200 orders, and it is 50 meters squared per gram that the particle surface of 407 Huangs amasss, and it is 65 meters squared per gram that 105 former red particle surfaces amass.
Embodiment 2
Butanone and n-propyl are made to mixed solvent, then get 5 parts of green light gold, be dissolved in 12 parts of mixed solvents, then to add successively in mixed solvent 20 parts of stand linseed oil, 4 part 407 yellow and 1 part 105 former red, it is fully stirred evenly.The temperature wherein stirring is 50 ℃, in mixed solvent, the weight ratio of butanone and n-propyl is 1:1, stand linseed oil is 40% vinylformic acid blending oil, the main component of 407 Huangs is Cadmium Sulfide, 105 former red main components are ferric oxide, green light gold adopts 1200 orders, and it is 50 meters squared per gram that the particle surface of 407 Huangs amasss, and it is 60 meters squared per gram that 105 former red particle surfaces amass.
Embodiment 3
Butanone and n-propyl are made to mixed solvent, then get 5 parts of green light gold, be dissolved in 13 parts of mixed solvents, then to add successively in mixed solvent 20 parts of stand linseed oil, 4 part 407 yellow and 1 part 105 former red, it is fully stirred evenly.The temperature wherein stirring is 60 ℃, in mixed solvent, the weight ratio of butanone and n-propyl is 1:1, stand linseed oil is 55% vinylformic acid blending oil, the main component of 407 Huangs is Cadmium Sulfide, 105 former red main components are ferric oxide, green light gold adopts 1200 orders, and it is 55 meters squared per gram that the particle surface of 407 Huangs amasss, and it is 70 meters squared per gram that 105 former red particle surfaces amass.
Claims (9)
1. prepare the method for blue or green gold ink for one kind, it is characterized in that butanone and n-propyl to make mixed solvent, then get 5 parts of green light gold, be dissolved in 11～13 parts of mixed solvents, again to add successively in mixed solvent 20 parts of stand linseed oil, 4 part 407 yellow and 1 part 105 former red, it is fully stirred evenly.
2. the method for the blue or green gold ink of preparation according to claim 1, is characterized in that, described whipping temp is 40～60 ℃.
3. the method for the blue or green gold ink of preparation according to claim 1, is characterized in that, in described mixed solvent, the weight ratio of butanone and n-propyl is 1:1.
4. the method for the blue or green gold ink of preparation according to claim 1, is characterized in that, the vinylformic acid blending oil that described stand linseed oil is 25-60%.
5. the method for the blue or green gold ink of preparation according to claim 1, is characterized in that, the main component of described 407 Huangs is Cadmium Sulfide.
6. the method for the blue or green gold ink of preparation according to claim 1, is characterized in that, described 105 former red main components are ferric oxide.
7. the method for the blue or green gold ink of preparation according to claim 1, is characterized in that, described green light gold adopts 1200 orders.
8. the method for the blue or green gold ink of preparation according to claim 1, is characterized in that,
Long-pending 50 meters squared per gram that are greater than of particle surface of described 407 Huangs.
9. the method for the blue or green gold ink of preparation according to claim 1, is characterized in that, long-pending 60 meters squared per gram that are greater than of described 105 former red particle surfaces.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410121559.XA CN103865325B (en) | 2014-03-28 | 2014-03-28 | A kind of method preparing blue or green gold ink |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410121559.XA CN103865325B (en) | 2014-03-28 | 2014-03-28 | A kind of method preparing blue or green gold ink |
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| CN103865325A true CN103865325A (en) | 2014-06-18 |
| CN103865325B CN103865325B (en) | 2016-01-06 |
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| Application Number | Title | Priority Date | Filing Date |
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| CN201410121559.XA Active CN103865325B (en) | 2014-03-28 | 2014-03-28 | A kind of method preparing blue or green gold ink |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106752360A (en) * | 2017-01-19 | 2017-05-31 | 长春吉星印务有限责任公司 | A kind of special solvent type gravure gold ink and preparation method thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001049162A (en) * | 1999-08-04 | 2001-02-20 | The Inctec Inc | Ink composition |
| CN101870833A (en) * | 2010-05-14 | 2010-10-27 | 红河雄风印业有限责任公司 | Gravure bronze printing ink without defects and lost points |
-
2014
- 2014-03-28 CN CN201410121559.XA patent/CN103865325B/en active Active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001049162A (en) * | 1999-08-04 | 2001-02-20 | The Inctec Inc | Ink composition |
| CN101870833A (en) * | 2010-05-14 | 2010-10-27 | 红河雄风印业有限责任公司 | Gravure bronze printing ink without defects and lost points |
Non-Patent Citations (1)
| Title |
|---|
| 王擢等: "《着色剂选用手册》", 31 August 2009, 化学工业出版社 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106752360A (en) * | 2017-01-19 | 2017-05-31 | 长春吉星印务有限责任公司 | A kind of special solvent type gravure gold ink and preparation method thereof |
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| Publication number | Publication date |
|---|---|
| CN103865325B (en) | 2016-01-06 |
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