CN101928510A - Flatting agent for UV cured leathers and preparation method thereof - Google Patents

Flatting agent for UV cured leathers and preparation method thereof Download PDF

Info

Publication number
CN101928510A
CN101928510A CN2010102968112A CN201010296811A CN101928510A CN 101928510 A CN101928510 A CN 101928510A CN 2010102968112 A CN2010102968112 A CN 2010102968112A CN 201010296811 A CN201010296811 A CN 201010296811A CN 101928510 A CN101928510 A CN 101928510A
Authority
CN
China
Prior art keywords
weight part
treatment agent
leather
delustring
delustring treatment
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.)
Pending
Application number
CN2010102968112A
Other languages
Chinese (zh)
Inventor
丁海燕
鄢红阳
帅宏喜
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
HANGZHOU ZFC NEW MATERIALS TECHNOLOGY Co Ltd
Original Assignee
HANGZHOU ZFC NEW MATERIALS TECHNOLOGY Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by HANGZHOU ZFC NEW MATERIALS TECHNOLOGY Co Ltd filed Critical HANGZHOU ZFC NEW MATERIALS TECHNOLOGY Co Ltd
Priority to CN2010102968112A priority Critical patent/CN101928510A/en
Publication of CN101928510A publication Critical patent/CN101928510A/en
Pending legal-status Critical Current

Links

Landscapes

  • Treatment And Processing Of Natural Fur Or Leather (AREA)

Abstract

The invention discloses a flatting agent for UV cured leathers and a preparation method thereof, and belongs to the field of after finishing of coatings, natural leathers, artificial leathers, synthetic leathers and textile fabrics. The flatting agent for the UV cured leathers comprises the following raw materials: 10 to 40 weight parts of prepolymer, 10 to 60 weight parts of active monomers, 2 to 10 weight parts of photoinitiator, 1 to 20 weight parts of coinitiator, 0.5 to 2 weight parts of defoamer, 0.1 to 1 weight part of leveling agent and 2 to 10 weight parts of flatting powder. The flatting agent for the UV cured leathers has the advantages of energy saving, environmental protection, high stability, good flatting effect and stable product quality.

Description

UV curable leather delustring treatment agent and preparation method thereof
Technical field
The present invention relates to a kind of UV curable leather delustring treatment agent and preparation method thereof, belong to finishing field behind coating, natural leather, leatheroid, synthetic leather, the weaving face fabric.
Background technology
The delustring treatment agent is a kind of novel functional coating, after the coating of delustring treatment agent, can give natural leather, leatheroid, synthetic leather and the weaving face fabric feel of soft exquisiteness naturally, and along with the variation of coated weight can also provide vision benefits such as soft light sensation, haze change.Traditional leather flatting processing mainly comprises following several: 1, oil soluble delustring treatment agent, the normally physical mixture of ordinary resin and mute light powder; 2, water-based delustring treatment agent, the normally physical mixture of water-based PA, PU resin and mute light powder.Oil soluble delustring treatment agent is a class the most traditional the most ancient treatment agent, and the application time is long, the market occupancy is big, and resulting extinction effect is comparatively stable, but solvent usually accounts for more than 70% of delustring treatment agent in oil soluble delustring treatment agent; Water-based delustring treatment agent is the novel product that a class newly developed in recent years substitutes oil soluble delustring treatment agent, the water-based matting agent is solvent with water, comparatively environmental protection, but owing to the affinity difference of water to the mute light powder of difference, stability, the extinction effect of water-based delustring treatment agent are all poor than solvent-borne type usually.
Oil soluble delustring treatment agent contains a large amount of solvents, and in use, there is bigger pollution in the volatilization of solvent and is difficult to relatively environment reclaims; The comparatively environmental protection of water-based matting agent, but poor stability, effect does not usually reach the level that substitutes the oil soluble matting agent fully, and because the evaporation of water enthalpy is big, specific heat capacity is high, needs more power consumption under the use technology identical with oil soluble delustring treatment agent.
Summary of the invention
Technical problem to be solved by this invention provide a kind of technological design rationally, the UV curable leather delustring treatment agent of good, the constant product quality of energy-conserving and environment-protective, good stability, extinction effect.
Another technical problem to be solved by this invention provide a kind of technological design rationally, the preparation method of constant product quality, the free of contamination UV curable leather of course of processing delustring treatment agent.
It is this UV curable leather delustring treatment agent that the present invention solves the problems of the technologies described above the technical scheme that is adopted, and its raw material composition is:
The flatting silica of the flow agent of the defoamer of the aided initiating of the light trigger of the reactive monomer of the prepolymer of 10-40 weight part, 10-60 weight part, 2-10 weight part, 1-20 weight part, 0.5-2 weight part, 0.1-1 weight part, 2-10 weight part.
As preferably, also comprise solvent in the raw material of the present invention, the amount of solvent is the 0-20 weight part, described solvent is in ethanol, Virahol, propyl carbinol, propylene glycol monomethyl ether, ethylene glycol monobutyl ether, methylethylketone, methyl iso-butyl ketone (MIBK), dimethylbenzene, vinyl acetic monomer, N-BUTYL ACETATE, chloroform, acetone, tetracol phenixin, pimelinketone, the tetrahydrofuran (THF), N, one or more mixtures of dinethylformamide, N,N-dimethylacetamide, dioxane, diacetone alcohol, ethylene glycol.
As preferably, prepolymer of the present invention is one or more the mixture in polyester acrylate, amino acrylates, urethane acrylate, bisphenol-a epoxy acrylate, fatty acid modified epoxy acrylate, the epoxy soybean oil acrylate.
As preferably, reactive monomer of the present invention is one or more the mixture in glycol diacrylate, hexanediyl ester, glycol ether diacrylate, Viscoat 295, tetramethylolmethane six acrylate, the pentanediol diacrylate.Play diluting effect and fast reaction speed.
As preferably, light trigger of the present invention is 907, one or more the mixture among ITX, BP, 1173,184, TPO, the OMBB.Main rising caused free radical and desiccation.
As preferably, aided initiating of the present invention is one or more the mixture among P-115, the EDAB.Rise and cooperate the initiator acting in conjunction.
As preferably, defoamer of the present invention is silicone based defoamer, is specially one or more the mixture among HX-2080, Fomax N, the KS-66.
As preferably, flow agent of the present invention is organic silicon modified by polyether, polyether siloxane copolymer, silicone copolymer.
As preferably, flatting silica of the present invention is superfine silicon dioxide, surface modification silicon-dioxide, superfine silicon dioxide is aerosil, the liquid phase silica of median size at the 0.01-5 micron, and surface modification silicon-dioxide is organic modification silicon-dioxide, wax improved silica.
The present invention solves the problems of the technologies described above the preparation method that the technical scheme that is adopted still is a kind of UV curable leather delustring treatment agent, and its processing step is:
A, be the prepolymer of 10-40 weight part with mass ratio, the reactive monomer of 10-60 weight part, the light trigger of 2-10 weight part, the aided initiating of 1-20 weight part, the defoamer of 0.5-2 weight part, the flow agent of 0.1-1 weight part, the flatting silica of 2-10 weight part, the 0-20 weight part, standby;
B, prepolymer, the reactive monomer of 20--100%, initiator, aided initiating, solvent with 20--100%, high-speed stirring, stirring velocity are 800-2000 rev/min, controlled temperature obtains intermediate raw material in that fully dissolving is extremely transparent fully below 70 ℃;
C, in intermediate raw material, add remaining prepolymer, remaining reactive monomer, defoamer, flow agent successively, stirred 5 minutes, add flatting silica, high speed dispersion 30-120 minute then, control speed 400-3500 rev/min, temperature is no more than 70 ℃ in the dispersion process, obtains UV curable leather delustring treatment agent.
The present invention compares with existing technology, has the following advantages and characteristics: (1) preparation method is simple, and the Device-General scope is wide.(2) solid part is high, and according to actual needs, prepared UV curable leather delustring treatment agent solid part can be solvent-free to 100% from 80%; (3) curing speed is fast, curing process is simple to operate, adopts the UV ultraviolet light polymerization, because it is fast not contain solvent more traditional delustring treatment agent set time, and does not need other subsequent techniques; (4) condition of cure is low, equipment is simple, and under the room temperature, control UV ultraviolet lamp intensity can conveniently be regulated curing speed; (5) environmental protection is stable, owing to can accomplish high contain admittedly even the agent of solvent-free relative oil soluble leather flatting, the agent of water-based leather flatting have lower energy consumption advantage, and because UV solidifies is a kind of chemical process, and the Chemical bond mode that is provided is effectively stable more than physical mixed.
Embodiment
The present invention is described in further detail below in conjunction with embodiment, and following examples are explanation of the invention and the present invention is not limited to following examples.
Embodiment 1
Get 15g two functionality polyester acrylates, 55g Viscoat 295,3g benzophenone, 1g tertiary amine acrylate, 0.25gHX-2080,0.25g Fomax N, 0.5g organic silicon modified by polyether flow agent and mix standbyly with 1000 rev/mins speed, guarantee in the mixing process that temperature is lower than 70 ℃; In said mixture, add remaining 15g two functionality polyester acrylates, with 1500 rev/mins speed, dispersing and mixing is even, adds 5g organic modification silicon-dioxide simultaneously, blending dispersion 30 minutes remains that temperature of charge is lower than 70 ℃ in the mixing process.Dispersion finishes, and discharging promptly gets UV curable leather delustring treatment agent.
Embodiment 2
Get 18g bisphenol-a epoxy acrylate, 18g tetramethylolmethane six acrylate, 1g1-hydroxyl cyclohexane phenyl ketone), 1g TPO(2,4,6-trimethylbenzoyl diphenyl phosphine oxide), 1g tertiary amine acrylate, 0.6g KS-66,0.4g polyether siloxane copolymer flow agent, 10g dimethylbenzene, mix standbyly with 800 rev/mins speed, guarantee in the mixing process that temperature is lower than 70 ℃; In said mixture, add 10g glycol diacrylate reactive monomer, 9g N-BUTYL ACETATE, mix with 2000 rev/mins speed, add 3.5g wax improved silica in the mixing process, blending dispersion 45 minutes remains that temperature of charge is lower than 70 ℃ in the mixing process.Dispersion finishes, and discharging promptly gets UV curable leather delustring treatment agent.
Embodiment 3
Get 20g urethane acrylate, 50g glycol ether diacrylate, 2.5g isopropyl thioxanthone, 1g 4-(N, the N-dimethylamino) ethyl benzoate, 1g Fomax N, 0.5g silicone copolymer flow agent, 3.5g N-BUTYL ACETATE, be mixed to transparent evenly standbyly with 600 rev/mins speed, mixing process guarantees that temperature of charge is lower than 70 ℃; In said mixture, add the fatty acid modified epoxy acrylic ester prepolymer of 15g, mix, add the 6.5g superfine silicon dioxide in the mixing process, disperseed 60 minutes, remain that temperature of charge is lower than 70 ℃ in the dispersing and mixing process with 1500 rev/mins speed.Dispersion finishes, and promptly gets UV curable leather delustring treatment agent.
Embodiment 4
Get 8g epoxy soybean oil acrylate, 3g pentanediol diacrylate, 8gOMBB, 10gP-115,5gEDAB, 0. 5gHX-2080,1g Fomax N, 0.3g organic silicon modified by polyether flow agent and mix standbyly with 1000 rev/mins speed, guarantee in the mixing process that temperature is lower than 70 ℃; In said mixture, add 32g bisphenol-a epoxy acrylate, 12 gram glycol ether diacrylates, 5 gram chloroforms, 2 gram acetone, speed with 1500 rev/mins, dispersing and mixing is even, add 2g organic modification silicon-dioxide simultaneously, blending dispersion 30 minutes remains that temperature of charge is lower than 70 ℃ in the mixing process.Dispersion finishes, and discharging promptly gets UV curable leather delustring treatment agent.
Embodiment 5
Get 10g bisphenol-a epoxy acrylate, 5g Viscoat 295,2g1173,2g184,8g tertiary amine acrylate, 1.2g KS-66,0.1g polyether siloxane copolymer flow agent, mix standbyly with 800 rev/mins speed, guarantee in the mixing process that temperature is lower than 70 ℃; In said mixture, add 27g urethane acrylate, 5g Viscoat 295, mix with 2000 rev/mins speed, add 8g wax improved silica in the mixing process, blending dispersion 45 minutes remains that temperature of charge is lower than 70 ℃ in the mixing process.Dispersion finishes, and discharging promptly gets UV curable leather delustring treatment agent.
Embodiment 6
Get 15g amino acrylates, 20g pentanediol diacrylate, 10g isopropyl thioxanthone, 20g 4-(N, the N-dimethylamino) ethyl benzoate, 2g Fomax N, 0.7g silicone copolymer flow agent, 5g dioxane, 5g diacetone alcohol, be mixed to transparent evenly standbyly with 600 rev/mins speed, mixing process guarantees that temperature of charge is lower than 70 ℃; In said mixture, add the fatty acid modified epoxy acrylic ester prepolymer of 10g, 10g Viscoat 295, mix with 1500 rev/mins speed, add the 6g superfine silicon dioxide in the mixing process, disperseed 60 minutes, and remained that temperature of charge was lower than 70 ℃ in the dispersing and mixing process.Dispersion finishes, and promptly gets UV curable leather delustring treatment agent.
Embodiment 7
Get 23g epoxy soybean oil acrylate, 20g pentanediol diacrylate, 20g glycol diacrylate, 5g BP, 6gP-115,0. 5gHX-2080,0.3g Fomax N, 1g organic silicon modified by polyether flow agent and mix standbyly with 1000 rev/mins speed, guarantee in the mixing process that temperature is lower than 70 ℃; Add 4g organic modification silicon-dioxide in said mixture, with 1500 rev/mins speed, dispersing and mixing is even, and blending dispersion 30 minutes remains that temperature of charge is lower than 70 ℃ in the mixing process.Dispersion finishes, and discharging promptly gets UV curable leather delustring treatment agent.
Embodiment 8
Get 8g bisphenol-a epoxy acrylate, 15g Viscoat 295,5g1173,4g184,4g tertiary amine acrylate, 1.8g KS-66,0.8g polyether siloxane copolymer flow agent, mix standbyly with 800 rev/mins speed, guarantee in the mixing process that temperature is lower than 70 ℃; In said mixture, add 2g urethane acrylate, 5g Viscoat 295, mix with 2000 rev/mins speed, add 3g wax improved silica in the mixing process, blending dispersion 45 minutes remains that temperature of charge is lower than 70 ℃ in the mixing process.Dispersion finishes, and discharging promptly gets UV curable leather delustring treatment agent.
Embodiment 9
Get the fatty acid modified epoxy acrylate of 12g, 10g pentanediol diacrylate, 7g isopropyl thioxanthone, 18g 4-(N, the N-dimethylamino) ethyl benzoate, 1.6g Fomax N, 0.6g silicone copolymer flow agent, be mixed to transparent evenly standbyly with 600 rev/mins speed, mixing process guarantees that temperature of charge is lower than 70 ℃; In said mixture, add the 35g Viscoat 295, mix, add the 7g superfine silicon dioxide in the mixing process, disperseed 60 minutes, remain that temperature of charge is lower than 70 ℃ in the dispersing and mixing process with 1500 rev/mins speed.Dispersion finishes, and promptly gets UV curable leather delustring treatment agent.
Embodiment 10
Get 30g amino acrylates, 35g pentanediol diacrylate, 6g isopropyl thioxanthone, 12g 4-(N, the N-dimethylamino) ethyl benzoate, 1.3g Fomax N, 0.9g silicone copolymer flow agent, 10g vinyl acetic monomer, 10g tetracol phenixin, be mixed to transparent evenly standbyly with 600 rev/mins speed, mixing process guarantees that temperature of charge is lower than 70 ℃; In said mixture, add the fatty acid modified epoxy acrylic ester prepolymer of 10g, mix, add the 10g superfine silicon dioxide in the mixing process, disperseed 60 minutes, remain that temperature of charge is lower than 70 ℃ in the dispersing and mixing process with 1500 rev/mins speed.Dispersion finishes, and promptly gets UV curable leather delustring treatment agent.Superfine silicon dioxide described in the above embodiment is aerosil, the liquid phase silica of median size at the 0.01-5 micron.
Among the present invention, it is coolings that prepolymer and reactive monomer divide the main purpose of two interpolations, to reacting basic not influence.
In addition, need to prove, the specific embodiment described in this specification sheets, its prescription, title that technology is named etc. can be different.Allly conceive equivalence or the simple change that described structure, feature and principle are done, be included in the protection domain of patent of the present invention according to patent of the present invention.The technician of the technical field of the invention can make various modifications or replenishes or adopt similar mode to substitute described specific embodiment; only otherwise depart from structure of the present invention or surmount the defined scope of these claims, all should belong to protection scope of the present invention.
Though the present invention with embodiment openly as above; but it is not in order to limit protection scope of the present invention; any technician who is familiar with this technology, change and the retouching done in not breaking away from design of the present invention and scope all should belong to protection scope of the present invention.

Claims (10)

1. UV curable leather delustring treatment agent, its raw material are formed:
The flatting silica of the flow agent of the defoamer of the aided initiating of the light trigger of the reactive monomer of the prepolymer of 10-40 weight part, 10-60 weight part, 2-10 weight part, 1-20 weight part, 0.5-2 weight part, 0.1-1 weight part, 2-10 weight part.
2. UV curable leather delustring treatment agent according to claim 1, it is characterized in that: also comprise solvent in the described raw material, the amount of solvent is the 0-20 weight part, described solvent is in ethanol, Virahol, propyl carbinol, propylene glycol monomethyl ether, ethylene glycol monobutyl ether, methylethylketone, methyl iso-butyl ketone (MIBK), dimethylbenzene, vinyl acetic monomer, N-BUTYL ACETATE, chloroform, acetone, tetracol phenixin, pimelinketone, the tetrahydrofuran (THF), N, one or more mixtures of dinethylformamide, N,N-dimethylacetamide, dioxane, diacetone alcohol, ethylene glycol.
3. UV curable leather delustring treatment agent according to claim 1 is characterized in that: described prepolymer is one or more the mixture in polyester acrylate, amino acrylates, urethane acrylate, bisphenol-a epoxy acrylate, fatty acid modified epoxy acrylate, the epoxy soybean oil acrylate.
4. UV curable leather delustring treatment agent according to claim 1 is characterized in that: described reactive monomer is one or more the mixture in glycol diacrylate, hexanediyl ester, glycol ether diacrylate, Viscoat 295, tetramethylolmethane six acrylate, the pentanediol diacrylate.
5. UV curable leather delustring treatment agent according to claim 1 is characterized in that: described light trigger is 907, one or more the mixture among ITX, BP, 1173,184, TPO, the OMBB.
6. UV curable leather delustring treatment agent according to claim 1 is characterized in that: described aided initiating is one or more the mixture among P-115, the EDAB.
7. UV curable leather delustring treatment agent according to claim 1, it is characterized in that: described defoamer is silicone based defoamer, is specially one or more the mixture among HX-2080, Fomax N, the KS-66.
8. UV curable leather delustring treatment agent according to claim 1, it is characterized in that: described flow agent is organic silicon modified by polyether, polyether siloxane copolymer, silicone copolymer.
9. UV curable leather delustring treatment agent according to claim 1, it is characterized in that: described flatting silica is superfine silicon dioxide, surface modification silicon-dioxide, superfine silicon dioxide is aerosil, the liquid phase silica of median size at the 0.01-5 micron, and surface modification silicon-dioxide is organic modification silicon-dioxide, wax improved silica.
10. the preparation method of a UV curable leather delustring treatment agent as claimed in claim 1, its processing step is:
A, be the prepolymer of 10-40 weight part with mass ratio, the reactive monomer of 10-60 weight part, the light trigger of 2-10 weight part, the aided initiating of 1-20 weight part, the defoamer of 0.5-2 weight part, the flow agent of 0.1-1 weight part, the flatting silica of 2-10 weight part, the 0-20 weight part, standby;
B, prepolymer, the reactive monomer of 20--100%, initiator, aided initiating, solvent with 20--100%, high-speed stirring, stirring velocity are 800-2000 rev/min, controlled temperature obtains intermediate raw material in that fully dissolving is extremely transparent fully below 70 ℃;
C, in intermediate raw material, add remaining prepolymer, remaining reactive monomer, defoamer, flow agent successively, stirred 5 minutes, add flatting silica, high speed dispersion 30-120 minute then, control speed 400-3500 rev/min, temperature is no more than 70 ℃ in the dispersion process, obtains UV curable leather delustring treatment agent.
CN2010102968112A 2010-09-29 2010-09-29 Flatting agent for UV cured leathers and preparation method thereof Pending CN101928510A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2010102968112A CN101928510A (en) 2010-09-29 2010-09-29 Flatting agent for UV cured leathers and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2010102968112A CN101928510A (en) 2010-09-29 2010-09-29 Flatting agent for UV cured leathers and preparation method thereof

Publications (1)

Publication Number Publication Date
CN101928510A true CN101928510A (en) 2010-12-29

Family

ID=43367950

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2010102968112A Pending CN101928510A (en) 2010-09-29 2010-09-29 Flatting agent for UV cured leathers and preparation method thereof

Country Status (1)

Country Link
CN (1) CN101928510A (en)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102839544A (en) * 2011-06-20 2012-12-26 杭州中富彩新材料科技有限公司 Ultra-foggy ultra-black delustering agent for leather and preparation method thereof
CN102898931A (en) * 2012-09-18 2013-01-30 无锡市中星工业胶带有限公司 Matte PC coiled material and preparation method thereof
CN103046377A (en) * 2012-12-28 2013-04-17 苏州鼎润复合材料有限公司 Cloudy-surface skin touch-feeling finishing agent for synthetic leather and surface treatment method of synthetic leather
WO2014029054A1 (en) * 2012-08-22 2014-02-27 江苏宝泽高分子材料股份有限公司 Skin-touch matte washing and brightening treatment agent for synthetic leather and preparation method thereof
CN104017487A (en) * 2014-06-18 2014-09-03 湖南松井新材料有限公司 Ultraviolet-curing matte paint
CN104212315A (en) * 2014-09-19 2014-12-17 江苏海晟涂料有限公司 Ultraviolet curing coating and preparation method thereof
WO2015196318A1 (en) * 2014-06-26 2015-12-30 江苏宝泽高分子材料股份有限公司 Discoloration polishing treatment agent for synthetic leather and preparation method for the agent
CN106700842A (en) * 2015-11-15 2017-05-24 惠州市长润发涂料有限公司 Ultraviolet-curable primer
CN106978048A (en) * 2017-03-29 2017-07-25 合肥天沃能源科技有限公司 A kind of energy saving paint and preparation method thereof
CN108486294A (en) * 2018-04-04 2018-09-04 江西三越新材料有限公司 UV type leather flatting inorganic agents and preparation method thereof
CN111748234A (en) * 2020-07-07 2020-10-09 威远达威木业有限公司 Cationic extinction filler and preparation method thereof
CN113308187A (en) * 2021-04-29 2021-08-27 江苏利田科技股份有限公司 Ultraviolet-curing leather hand feeling coating agent and preparation method thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1477168A (en) * 2002-08-20 2004-02-25 北京英力科技发展有限公司 Photocurable water coating agent
CN101423676A (en) * 2008-12-18 2009-05-06 江南大学 Method for preparing non-toxic visible ultraviolet heat insulating UV coating material
CN101805560A (en) * 2010-03-30 2010-08-18 上海长悦涂料有限公司 Ultraviolet light curing memory type paint and preparation method thereof
CN201566396U (en) * 2009-12-08 2010-09-01 李树森 UV curing colored PVC decorative sheet

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1477168A (en) * 2002-08-20 2004-02-25 北京英力科技发展有限公司 Photocurable water coating agent
CN101423676A (en) * 2008-12-18 2009-05-06 江南大学 Method for preparing non-toxic visible ultraviolet heat insulating UV coating material
CN201566396U (en) * 2009-12-08 2010-09-01 李树森 UV curing colored PVC decorative sheet
CN101805560A (en) * 2010-03-30 2010-08-18 上海长悦涂料有限公司 Ultraviolet light curing memory type paint and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
刘登良: "《涂料工艺》", 31 January 2010, article "光固化涂料用活性稀释剂", pages: 612-617 *

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102839544A (en) * 2011-06-20 2012-12-26 杭州中富彩新材料科技有限公司 Ultra-foggy ultra-black delustering agent for leather and preparation method thereof
WO2014029054A1 (en) * 2012-08-22 2014-02-27 江苏宝泽高分子材料股份有限公司 Skin-touch matte washing and brightening treatment agent for synthetic leather and preparation method thereof
CN102898931B (en) * 2012-09-18 2016-04-13 无锡市中星工业胶带有限公司 A kind of matte PC membrane and preparation method thereof
CN102898931A (en) * 2012-09-18 2013-01-30 无锡市中星工业胶带有限公司 Matte PC coiled material and preparation method thereof
CN103046377A (en) * 2012-12-28 2013-04-17 苏州鼎润复合材料有限公司 Cloudy-surface skin touch-feeling finishing agent for synthetic leather and surface treatment method of synthetic leather
CN104017487A (en) * 2014-06-18 2014-09-03 湖南松井新材料有限公司 Ultraviolet-curing matte paint
CN104017487B (en) * 2014-06-18 2017-01-04 湖南松井新材料有限公司 Ultraviolet light cured burnished paint
WO2015196318A1 (en) * 2014-06-26 2015-12-30 江苏宝泽高分子材料股份有限公司 Discoloration polishing treatment agent for synthetic leather and preparation method for the agent
CN104212315A (en) * 2014-09-19 2014-12-17 江苏海晟涂料有限公司 Ultraviolet curing coating and preparation method thereof
CN106700842A (en) * 2015-11-15 2017-05-24 惠州市长润发涂料有限公司 Ultraviolet-curable primer
CN106978048A (en) * 2017-03-29 2017-07-25 合肥天沃能源科技有限公司 A kind of energy saving paint and preparation method thereof
CN108486294A (en) * 2018-04-04 2018-09-04 江西三越新材料有限公司 UV type leather flatting inorganic agents and preparation method thereof
CN111748234A (en) * 2020-07-07 2020-10-09 威远达威木业有限公司 Cationic extinction filler and preparation method thereof
CN113308187A (en) * 2021-04-29 2021-08-27 江苏利田科技股份有限公司 Ultraviolet-curing leather hand feeling coating agent and preparation method thereof

Similar Documents

Publication Publication Date Title
CN101928510A (en) Flatting agent for UV cured leathers and preparation method thereof
CN105968253B (en) It is a kind of water-based from mat acrylic emulsion and preparation method and application
CN101845258B (en) Low-volatility and quick-drying aqueous toy coating and preparation method thereof
CN103602224B (en) A kind of white solvent-free finish paint and its preparation method and construction technology
CN105062405A (en) LED photocuring non-solvent type photosensitive transfer printing adhesive for cover plate glass substrate and preparation method thereof
CN102199375B (en) Ultraviolet (UV) paint solidified by ultraviolet light
CN104387945A (en) Odorless staining-resistant anti-yellowing UV coated matt finish paint coating, and preparation method and construction technology thereof
CN105038575A (en) Water-based anti-dazzle UV coating, hard coated film and preparation method of hard coated film
CN102977748B (en) A kind of not containing the UV furniture spray paint light top coat top coat of volatile organic solvent
CN104479523A (en) Highly hydrophobicuv (ultraviolet) leather surface treating agent and preparation method thereof
CN103589324A (en) UV (ultraviolet) anti-scratch matte finishing paint
CN102516837A (en) Ultraviolet (UV) cured roller coating embellishing clear finish coating
CN101591484A (en) A kind of photocureable coating for pianos
CN110229317B (en) UV-curable unsaturated polyester resin with high vinyl functionality, and preparation method and application thereof
CN105199040A (en) Organic silicone modified acrylate emulsion and preparation method thereof
CN109749509A (en) One kind having snowflake special-effect LED-UV ink and preparation method thereof
CN101343525A (en) Watersoluble adhesive agent used in imitation leather electrostatic real leather embedding product and preparation thereof
CN109796553A (en) Solvent-free lotion of the low environment-friendly type aqueous acrylate of smell and preparation method thereof
CN106832080A (en) A kind of woodcare paint styrene-acrylate core/shell emulsion and preparation method thereof
CN102807814B (en) Nano silica-modified recoatable ultraviolet (UV) varnish used on plastic and preparation method for varnish
CN103113822B (en) Ultraviolet light curable coating with dewdrop effect and preparation method and coating method thereof
CN111718647B (en) Environment-friendly water-based UV coating and preparation method thereof
CN105273612A (en) UV coating for glass
CN109868051A (en) A kind of wooden furniture high aloof from politics and material pursuits polyurethane matte finishing coat of high-solid lower-viscosity and preparation method thereof
CN113603821A (en) Acrylic emulsion for weather-resistant cross-linked soft porcelain and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C12 Rejection of a patent application after its publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20101229