CN115725213A - Ultraviolet absorption finishing paint - Google Patents
Ultraviolet absorption finishing paint Download PDFInfo
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- CN115725213A CN115725213A CN202211537254.8A CN202211537254A CN115725213A CN 115725213 A CN115725213 A CN 115725213A CN 202211537254 A CN202211537254 A CN 202211537254A CN 115725213 A CN115725213 A CN 115725213A
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- 239000003973 paint Substances 0.000 title claims abstract description 45
- 238000010521 absorption reaction Methods 0.000 title claims abstract description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 47
- 239000006097 ultraviolet radiation absorber Substances 0.000 claims abstract description 41
- 238000000576 coating method Methods 0.000 claims abstract description 20
- 239000004611 light stabiliser Substances 0.000 claims abstract description 20
- 229940124543 ultraviolet light absorber Drugs 0.000 claims abstract description 18
- 239000000839 emulsion Substances 0.000 claims abstract description 12
- 239000002562 thickening agent Substances 0.000 claims abstract description 12
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 11
- 239000010703 silicon Substances 0.000 claims abstract description 11
- 239000000080 wetting agent Substances 0.000 claims abstract description 10
- 239000013530 defoamer Substances 0.000 claims abstract description 6
- 239000002202 Polyethylene glycol Substances 0.000 claims description 21
- 229920001223 polyethylene glycol Polymers 0.000 claims description 21
- 229940116351 sebacate Drugs 0.000 claims description 15
- 239000002966 varnish Substances 0.000 claims description 15
- 239000011248 coating agent Substances 0.000 claims description 14
- 239000002250 absorbent Substances 0.000 claims description 13
- 230000002745 absorbent Effects 0.000 claims description 13
- VMRIVYANZGSGRV-UHFFFAOYSA-N 4-phenyl-2h-triazin-5-one Chemical compound OC1=CN=NN=C1C1=CC=CC=C1 VMRIVYANZGSGRV-UHFFFAOYSA-N 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 9
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 239000003755 preservative agent Substances 0.000 claims description 7
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 6
- 230000002335 preservative effect Effects 0.000 claims description 6
- 229940123457 Free radical scavenger Drugs 0.000 claims description 5
- 150000001412 amines Chemical class 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 239000002516 radical scavenger Substances 0.000 claims description 5
- ZSSVCEUEVMALRD-UHFFFAOYSA-N 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(octyloxy)phenol Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C1=NC(C=2C(=CC(C)=CC=2)C)=NC(C=2C(=CC(C)=CC=2)C)=N1 ZSSVCEUEVMALRD-UHFFFAOYSA-N 0.000 claims description 4
- 239000007983 Tris buffer Substances 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 4
- 230000000996 additive effect Effects 0.000 claims description 4
- 239000002518 antifoaming agent Substances 0.000 claims description 4
- 238000004806 packaging method and process Methods 0.000 claims description 3
- 230000002528 anti-freeze Effects 0.000 claims description 2
- 238000005189 flocculation Methods 0.000 claims description 2
- 230000016615 flocculation Effects 0.000 claims description 2
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 claims 1
- 238000007710 freezing Methods 0.000 claims 1
- 239000012860 organic pigment Substances 0.000 abstract description 15
- 238000005562 fading Methods 0.000 abstract description 10
- 230000003111 delayed effect Effects 0.000 abstract description 2
- 238000005259 measurement Methods 0.000 abstract description 2
- 230000000052 comparative effect Effects 0.000 description 10
- 238000000034 method Methods 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 238000004383 yellowing Methods 0.000 description 5
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- HTTGVORJOBRXRJ-UHFFFAOYSA-N 2-(triazin-4-yl)phenol Chemical class OC1=CC=CC=C1C1=CC=NN=N1 HTTGVORJOBRXRJ-UHFFFAOYSA-N 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 229910000838 Al alloy Inorganic materials 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
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- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- AZXGXVQWEUFULR-UHFFFAOYSA-N 2',4',5',7'-tetrabromofluorescein Chemical compound OC(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C(O)=C(Br)C=C21 AZXGXVQWEUFULR-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical group CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- HBHZKFOUIUMKHV-UHFFFAOYSA-N chembl1982121 Chemical compound OC1=CC=C2C=CC=CC2=C1N=NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O HBHZKFOUIUMKHV-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
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- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
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- 231100000956 nontoxicity Toxicity 0.000 description 1
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Abstract
The invention relates to the technical field of coatings, and discloses an ultraviolet-absorbing finishing paint. The finishing paint mainly comprises, by mass, 500-600 parts of water-based organic silicon modified acrylic emulsion, 400-500 parts of water, 5-10 parts of water-based ultraviolet light absorber 1, 10-20 parts of water-based ultraviolet light absorber 2, 4-5 parts of water-based light stabilizer, 5-10 parts of thickener, 1-2 parts of defoamer, 20-30 parts of film-forming assistant, 2-3 parts of wetting agent and 1-2 parts of multifunctional assistant. The ultraviolet absorption finishing paint provided by the invention can effectively prevent the fading of the paint containing the organic pigment, and the fading time of the organic pigment can be delayed by more than 2 times by actual measurement.
Description
Technical Field
The invention relates to the technical field of coatings, in particular to an ultraviolet absorption finishing paint for slowing down fading of organic pigments.
Background
The finishing varnish is commonly called gloss oil and has very high use frequency in model making. Is generally used for civil models to improve the brightness of finished products. The currently common finishing paints include automobile finishing paints, exterior wall transparent finishing paints, metal finishing paints and the like, and are divided into polyurethane finishing paints, fluorocarbon finishing paints, high-hardness glass finishing paints and the like according to different raw materials of the finishing paints. The ideal finishing paint should have the properties of transparency, no yellowing, ultraviolet resistance, abrasion resistance, chemical resistance and the like, and also should have high gloss and high gloss retention for use on various worn surfaces for decoration and protection.
At present, various coatings containing organic pigments are increasingly used, and the organic pigments have bright colors, strong tinting strength and no toxicity, but are often inferior to inorganic pigments in light resistance, heat resistance, solvent resistance and migration resistance. Although some existing anti-yellowing finishing paints improve the product performance by adding an ultraviolet absorbent, a light stabilizer and the like to improve the finishing paint, the improvement of the performance is only the improvement of the yellowing performance of the finishing paint, and the fading improvement effect of the coated organic pigment is not obvious. Even if various coatings of the organic pigment are decorated and protected by adopting the yellowing-resistant and ultraviolet-resistant finishing paint, the better effect of preventing the fading of the organic pigment cannot be achieved.
The prior yellowing-resistant ultraviolet-resistant finishing varnish can be referred to Chinese patent application with publication numbers of CN110922830A, CN103387655A, CN106349848A and the like.
Disclosure of Invention
The invention aims to provide an ultraviolet absorption finishing paint capable of effectively delaying the fading time of organic pigments, and at least provides a beneficial choice or creation condition for solving one or more technical problems in the prior art.
In order to achieve the purpose, the invention adopts the following technical scheme.
An ultraviolet absorption finishing paint mainly comprises the following components in parts by mass: 500-600 parts of water-based organic silicon modified acrylic emulsion, 400-500 parts of water, 5-10 parts of water-based ultraviolet light absorber 1, 10-20 parts of water-based ultraviolet light absorber 2, 4-5 parts of water-based light stabilizer, 5-10 parts of thickener, 1-2 parts of defoamer, 20-30 parts of film-forming assistant, 2-3 parts of wetting agent and 1-2 parts of multifunctional assistant.
Wherein the ultraviolet absorbent 1 is an ultraviolet absorbent of hydroxyphenyl-phenylpropriazole type, and is composed of 45-55 wt% of 3- [3- (2-H-benzotriazol-2-yl) -4-hydroxy-5-tert-butylphenyl ] -propionic acid-polyethylene glycol 300-ester, 35-40 wt% of 3- [3- (2-H-benzotriazol-2-yl) -4-hydroxy-5-tert-butylphenyl ] -propionic acid } -polyethylene glycol 300-ester and 10-15 wt% of polyethylene glycol.
The ultraviolet absorbent 2 is a Hydroxyphenyltriazine (HPT) ultraviolet absorbent.
The water-based light stabilizer is formed by mixing 70-85wt% of bis (1, 2, 6-pentamethyl-4-piperidyl) sebacate and 15-30wt% of methyl-1, 2, 6-pentamethyl-4-piperidyl sebacate and serves as a liquid hindered amine free radical scavenger of the coating.
More preferably, the ultraviolet absorber 1 is composed of 50% by weight of 3- [3- (2-H-benzotriazol-2-yl) -4-hydroxy-5-t-butylphenyl ] -propionic acid-polyethylene glycol 300-ester, 38% by weight of 3- [3- (2-H-benzotriazol-2-yl) -4-hydroxy-5-t-butylphenyl ] -propionic acid } -polyethylene glycol 300-ester and 12% of polyethylene glycol.
More preferably, the ultraviolet absorber 2 is 3 oxazine-5, 4, 6-tris (2 '-hydroxy-4' -n-butoxyphenyl), CAS:63856-18-8.
More preferably, the ultraviolet absorber 2 is an ultraviolet absorber UV-1164.
More preferably, the aqueous light stabilizer is a mixture of 80wt% bis (1, 2, 6-pentamethyl-4-piperidinyl) sebacate and 20wt% methyl-1, 2, 6-pentamethyl-4-piperidinyl sebacate.
More preferably, the ultraviolet absorption finishing paint further comprises 10-20 parts of an antifreezing agent by mass.
More preferably, the ultraviolet absorption finishing paint further comprises 1-2 parts of mildew-proof preservative by mass.
When the ultraviolet absorption finishing paint is prepared, the method comprises the following steps: 1) Premixing the thickening agent with 5-10 parts of water to ensure that the thickening agent does not flocculate or agglomerate; 2) Adding the rest water, the water-based organic silicon modified acrylic emulsion, the defoaming agent, the film forming aid, the wetting agent and the multifunctional aid, and uniformly mixing; 3) Adding the aqueous ultraviolet light absorber 1, the aqueous ultraviolet light absorber 2 and the aqueous light stabilizer, and uniformly mixing; 4) And (5) inspecting, otherwise disposing unqualified products, and packaging qualified products to obtain finished ultraviolet absorption finishing paint products.
More preferably, 10-20 parts of an antifreezing agent is also added in the step 2).
More preferably, 1-2 parts of mildew-proof preservative is also added in the step 2).
The invention adopts the technical scheme and at least has the following beneficial effects.
According to the ultraviolet absorption finishing paint provided by the invention, the specific ultraviolet absorber 1, the specific ultraviolet absorber 2 and the specific light stabilizer are added into the aqueous organic silicon modified acrylic emulsion based finishing paint, so that the fading of the coating containing the organic pigment can be effectively prevented, and the fading time of the organic pigment can be delayed by more than 2 times through actual measurement.
Detailed Description
The following further describes the embodiments of the present invention, so that the technical solutions and the advantages thereof of the present invention are more clear and definite. The following description of the embodiments is exemplary in nature and is in no way intended to limit the invention, as defined by the appended claims.
Additional aspects and advantages of the invention will be set forth in part in the description which follows, and in part will be obvious from the description, or may be learned by practice of the invention.
Example 1.
An ultraviolet absorption finishing paint mainly comprises the following components in parts by mass: 550 parts of water-based organic silicon modified acrylic emulsion, 450 parts of water, 8 parts of water-based ultraviolet light absorber 1, 15 parts of water-based ultraviolet light absorber 2, 5 parts of water-based light stabilizer, 8 parts of thickener, 2 parts of defoamer, 25 parts of film-forming assistant, 2 parts of wetting agent and 2 parts of multifunctional assistant.
Wherein the ultraviolet absorber 1 is an ultraviolet absorber of hydroxyphenyl-phenylpropriazole type, and is composed of 50 wt% of 3- [3- (2-H-benzotriazol-2-yl) -4-hydroxy-5-tert-butylphenyl ] -propionic acid-polyethylene glycol 300-ester, 38 wt% of 3- [3- (2-H-benzotriazol-2-yl) -4-hydroxy-5-tert-butylphenyl ] -propionic acid } -polyethylene glycol 300-ester and 12% of polyethylene glycol.
The ultraviolet absorbent 2 is a Hydroxyphenyltriazine (HPT) ultraviolet absorbent, the main component of which is a 2-hydroxy-phenyl-triazine derivative. Preferably 3 oxazine-5, 4, 6-tris (2 '-hydroxy-4' -n-butoxyphenyl), CAS:63856-18-8.
The water-based light stabilizer is formed by mixing 80wt% of bis (1, 2, 6-pentamethyl-4-piperidyl) sebacate and 20wt% of methyl-1, 2, 6-pentamethyl-4-piperidyl sebacate and serves as a liquid hindered amine free radical scavenger of the coating.
The other components are all conventional reagents in the market. Wherein, the water-based organic silicon modified acrylic emulsion adopts low VOC water-based silicone-acrylate emulsion, and has strong cohesiveness and good weather resistance. The thickening agent is a polyurethane rheological thickening agent and is used for improving the viscosity of a coating system, improving the thixotropy of the coating, preventing sedimentation and ensuring that the coating does not sag. The film forming additive is a high-boiling-point zero-VOC film forming additive, so that the low-temperature film forming performance is ensured. The defoaming agent is used for defoaming and inhibiting foam, the wetting agent is used for improving the hydrophilicity of the coating system, and the multifunctional auxiliary agent is preferably AMP95 multifunctional auxiliary agent which is used for stabilizing the pH value of the coating system.
When the ultraviolet absorption finishing paint is prepared, the method comprises the following steps: 1) Premixing the thickening agent and 5-10 parts of water to ensure that flocculation and caking are avoided; 2) Adding the rest water, the water-based organic silicon modified acrylic emulsion, the defoaming agent, the film forming aid, the wetting agent and the multifunctional aid, and uniformly mixing; 3) Adding the aqueous ultraviolet light absorber 1, the aqueous ultraviolet light absorber 2 and the aqueous light stabilizer, and uniformly mixing; 4) And (5) inspecting, otherwise disposing the unqualified product, and packaging the qualified product to obtain the finished product 1 of the ultraviolet absorption finishing paint.
Example 2.
An ultraviolet absorption finishing paint mainly comprises the following components in parts by mass: 500 parts of water-based organic silicon modified acrylic emulsion, 500 parts of water, 10 parts of water-based ultraviolet light absorber 1, 10 parts of water-based ultraviolet light absorber 2,4 of water-based light stabilizer, 10 parts of thickener, 1 part of defoamer, 20 parts of film-forming assistant, 2 parts of wetting agent and 1 part of multifunctional assistant.
Wherein the ultraviolet absorber 1 is an ultraviolet absorber of hydroxyphenyl-phenylpropriazole type, and is composed of 45 wt% of 3- [3- (2-H-benzotriazol-2-yl) -4-hydroxy-5-tert-butylphenyl ] -propionic acid-polyethylene glycol 300-ester, 40 wt% of 3- [3- (2-H-benzotriazol-2-yl) -4-hydroxy-5-tert-butylphenyl ] -propionic acid } -polyethylene glycol 300-ester and 15wt% of polyethylene glycol.
The ultraviolet absorbent 2 is a Hydroxyphenyltriazine (HPT) ultraviolet absorbent, the main component of which is a 2-hydroxy-phenyl-triazine derivative, preferably 2- [4, 6-bis (2, 4-dimethylphenyl) -1,3, 5-triazin-2-yl ] -5-octyloxyphenol (ultraviolet absorbent UV-1164).
The water-based light stabilizer is formed by mixing 85wt% of bis (1, 2, 6-pentamethyl-4-piperidyl) sebacate and 15wt% of methyl-1, 2, 6-pentamethyl-4-piperidyl sebacate and serves as a liquid hindered amine free radical scavenger of the coating.
The other components are all conventional reagents in the market. The preparation method is consistent with that of example 1, and finally the finished product 2 of the ultraviolet absorption finishing paint is obtained.
Example 3.
An ultraviolet absorption finishing paint mainly comprises the following components in parts by mass: 600 parts of water-based organic silicon modified acrylic emulsion, 400 parts of water, 5 parts of water-based ultraviolet light absorber 1, 20 parts of water-based ultraviolet light absorber 2,4 parts of water-based light stabilizer, 10 parts of thickener, 2 parts of defoamer, 30 parts of film-forming assistant, 1 part of wetting agent and 1 part of multifunctional assistant.
Wherein the ultraviolet absorber 1 is an ultraviolet absorber of hydroxyphenyl-phenylpropriazole type, and is composed of 55 wt% of 3- [3- (2-H-benzotriazol-2-yl) -4-hydroxy-5-tert-butylphenyl ] -propionic acid-polyethylene glycol 300-ester, 35 wt% of 3- [3- (2-H-benzotriazol-2-yl) -4-hydroxy-5-tert-butylphenyl ] -propionic acid } -polyethylene glycol 300-ester and 10 wt% of polyethylene glycol.
The ultraviolet absorber 2 is a Hydroxyphenyltriazine (HPT) ultraviolet absorber, mainly a 2-hydroxy-phenyl-triazine derivative. Preferably 3 oxazine-5, 4, 6-tris (2 '-hydroxy-4' -n-butoxyphenyl), CAS:63856-18-8.
The water-based light stabilizer is formed by mixing 70wt% of bis (1, 2, 6-pentamethyl-4-piperidyl) sebacate and 30wt% of methyl-1, 2, 6-pentamethyl-4-piperidyl sebacate and serves as a liquid hindered amine free radical scavenger of the coating.
The other components are all conventional reagents sold in the market. The preparation method is consistent with that of example 1, and finally the finished product 3 of the ultraviolet absorption finishing paint is obtained.
Example 4.
The components and the preparation method of the ultraviolet absorption finishing paint are consistent with those of example 1, except that 15 parts of antifreezing agent is further contained in the components, and finally, a finished product 4 of the ultraviolet absorption finishing paint is obtained.
The antifreezing agent is a conventional reagent sold in the market, preferably a zero VOC, odorless and high-efficiency water-based antifreezing agent, and ensures the low-temperature stability of the coating.
In some embodiments, the amount of the antifreeze added may be appropriately adjusted between 10 to 20 parts and is not limited to the present embodiment.
Example 5.
The components and the preparation method of the ultraviolet absorption finishing paint are the same as those in example 1, and the difference is that the components also contain 1 part of mildew-proof preservative, and finally, a finished product 5 of the ultraviolet absorption finishing paint is obtained.
Mildew-proof preservatives are commercially available conventional agents used to prevent the mildew-forming action of coatings/lacquers.
In some embodiments, the addition amount of the mildew-proof preservative can be properly adjusted according to actual needs, such as 2 parts and the like; the present embodiment is not limited.
Comparative example 1.
An ultraviolet-absorbing overprint varnish having the composition and the production method in accordance with example 1, except that the addition of the aqueous ultraviolet absorber 1 was omitted and the amount of the aqueous ultraviolet absorber 2 was increased to 23 parts; comparative sample 1 was obtained.
Comparative example 2.
An ultraviolet-absorbing overprint varnish having the composition and the production method in accordance with example 1, except that the addition of the aqueous ultraviolet absorber 2 was omitted and the amount of the aqueous ultraviolet absorber 1 was increased to 23 parts; comparative sample 2 was obtained.
Comparative example 3.
A non-ultraviolet-absorbing overprint varnish having the same composition and preparation method as in example 1 except that the addition of an aqueous ultraviolet absorber 1, an aqueous ultraviolet absorber 2 and an aqueous light stabilizer was omitted from the composition, to obtain a comparative sample 3.
Comparative example 4.
A UV-absorbing overprint varnish was prepared in accordance with example 1 except that the light stabilizer in the composition was changed to methyl-1, 2, 6-pentamethyl-4-piperidyl sebacate at 100% by weight, and comparative sample 4 was obtained.
To better demonstrate the advancement of the present invention, the organic pigment fading resistance test was carried out by applying the overprint varnishes prepared in examples 1 to 5 and comparative examples 1 to 4, respectively, to the outside of the organic pigment-containing coating material.
The specific test method is as follows.
1) Three acrylic resin paints containing gold light red (c.i. pigment red 21), phthalocyanine blue (c.i. pigment blue 15), permanent orange HSL (c.i. pigment orange 36), respectively, were prepared. The three prepared acrylic acid coatings are respectively coated on the surfaces of three different aluminum alloy plates and cured. And respectively coating the finishing paints of examples 1-5 and comparative examples 1-4 on different areas of the surface of each aluminum alloy plate, and curing.
2) And (3) aging test: and (4) carrying out an aging test by adopting an ultraviolet artificial climate aging test box.
The test results are shown in table 1.
Table 1, organic pigment fade resistance test comparison.
As can be seen from Table 1, the UV-absorbing overprint varnish prepared by the present invention can effectively delay the fading time of organic pigments.
It should be noted that, the technical features of the above embodiments may be arbitrarily combined, and for the sake of brevity, all possible combinations of the technical features in the above embodiments are not described, but should be considered as the scope of the present specification as long as there is no contradiction between the combinations of the technical features.
The above examples only show some embodiments of the present invention, and the description thereof is more specific and detailed, but not construed as limiting the scope of the invention. It should be noted that various changes and modifications can be made by those skilled in the art without departing from the spirit of the invention, and these changes and modifications are all within the scope of the invention. The parts not described in the specific embodiments are all the prior art or common general knowledge.
It should also be noted that in the description of the present invention, the contents of the present invention can be more easily understood by referring to the detailed description of the preferred embodiments of the present invention and the examples included therein. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. In case of conflict, the present specification, including definitions, will control.
In the present invention, the term "prepared from" \8230 ", is used synonymously with" comprising ". The terms "comprises," "comprising," "includes," "including," "has," "having," "contains" or any other variation thereof, as used herein, are intended to cover a non-exclusive inclusion. For example, a composition, process, method, article, or apparatus that comprises a list of elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherent to such composition, process, method, article, or apparatus.
In the present invention, when an equivalent, concentration, or other value or parameter is expressed as a range, preferred range, or as a range defined by a list of upper preferable values and lower preferable values, this is to be understood as specifically disclosing all ranges formed from any pair of any upper range limit or preferred value and any lower range limit or preferred value, regardless of whether ranges are separately disclosed. For example, when the range "1 to 5" is disclosed, the described range should be interpreted to include the ranges "1 to 4", "1 to 3", "1 to 2 and 4 to 5", "1 to 3 and 5", and the like. When a range of values is described herein, unless otherwise specified, the range is intended to include the endpoints thereof, and all integers and fractions within the range.
In addition, the indefinite articles "a" and "an" preceding an element or component of the invention are intended to have no limitation on the number (i.e., number of occurrences) of the element or component. Thus, "a" or "an" should be read to include one or at least one, and the singular form of an element or component also includes the plural unless the number clearly indicates the singular.
Claims (10)
1. An ultraviolet absorption finishing paint mainly comprises the following components in parts by mass: 500-600 parts of water-based organic silicon modified acrylic emulsion, 400-500 parts of water, 5-10 parts of water-based ultraviolet light absorber 1, 10-20 parts of water-based ultraviolet light absorber 2, 4-5 parts of water-based light stabilizer, 5-10 parts of thickener, 1-2 parts of defoamer, 20-30 parts of film-forming assistant, 2-3 parts of wetting agent and 1-2 parts of multifunctional assistant;
it is characterized in that the preparation method is characterized in that,
the ultraviolet absorbent 1 is an ultraviolet absorbent of hydroxyphenyl-phenylpropriazole class, and consists of 45-55 wt% of 3- [3- (2-H-benzotriazole-2-yl) -4-hydroxy-5-tert-butylphenyl ] -propionic acid-polyethylene glycol 300-ester, 35-40 wt% of 3- [3- (2-H-benzotriazole-2-yl) -4-hydroxy-5-tert-butylphenyl ] -propionic acid } -polyethylene glycol 300-ester and 10-15 wt% of polyethylene glycol;
the ultraviolet absorbent 2 is a hydroxyphenyl triazine (HPT) ultraviolet absorbent;
the water-based light stabilizer is formed by mixing 70-85wt% of bis (1, 2, 6-pentamethyl-4-piperidyl) sebacate and 15-30wt% of methyl-1, 2, 6-pentamethyl-4-piperidyl sebacate and serves as a liquid hindered amine free radical scavenger of the coating.
2. The UV-absorbing overprint varnish of claim 1, wherein the UV absorber 1 consists of 50 wt% of 3- [3- (2-H-benzotriazol-2-yl) -4-hydroxy-5-tert-butylphenyl ] -propionic acid-polyethylene glycol 300-ester, 38 wt% of 3- [3- (2-H-benzotriazol-2-yl) -4-hydroxy-5-tert-butylphenyl ] -propionic acid } -polyethylene glycol 300-ester and 12% of polyethylene glycol.
3. The ultraviolet-absorbing overprint varnish of claim 1, wherein the ultraviolet absorber 2 is 3 oxazine-5, 4, 6-tris (2 '-hydroxy-4' -n-butoxyphenyl), CAS:63856-18-8.
4. The ultraviolet absorbing overprint varnish of claim 1, wherein the ultraviolet absorber 2 is an ultraviolet absorber UV-1164.
5. The UV-absorbing overprint varnish of claim 1, wherein the aqueous light stabilizer is a mixture of 80wt% bis (1, 2, 6-pentamethyl-4-piperidinyl) sebacate and 20wt% methyl-1, 2, 6-pentamethyl-4-piperidinyl sebacate.
6. The ultraviolet-absorbing overprint varnish according to claim 1, further comprising 10 to 20 parts by mass of an antifreeze.
7. The ultraviolet-absorbing finishing paint as claimed in claim 1, further comprising 1-2 parts by mass of a mildewproof preservative.
8. The ultraviolet-absorbing overprint varnish of claim 1, comprising the steps of:
1) Premixing the thickening agent and 5-10 parts of water to ensure that flocculation and caking are avoided;
2) Adding the rest water, the water-based organic silicon modified acrylic emulsion, the defoaming agent, the film forming additive, the wetting agent and the multifunctional additive, and uniformly mixing;
3) Adding the aqueous ultraviolet light absorber 1, the aqueous ultraviolet light absorber 2 and the aqueous light stabilizer, and uniformly mixing;
4) And (5) inspecting, otherwise disposing unqualified products, and packaging qualified products to obtain finished ultraviolet absorption finishing paint products.
9. The ultraviolet absorbing overprint varnish of claim 8, wherein 10 to 20 parts of an anti-freezing agent is further added in step 2).
10. The ultraviolet absorbing finishing paint of claim 8 further comprising 1 to 2 parts of a mildew-proof preservative in step 2).
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CN202211537254.8A CN115725213A (en) | 2022-12-02 | 2022-12-02 | Ultraviolet absorption finishing paint |
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CN202211537254.8A CN115725213A (en) | 2022-12-02 | 2022-12-02 | Ultraviolet absorption finishing paint |
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KR20200129066A (en) * | 2016-12-16 | 2020-11-17 | 임상택 | Gloss varnish with excellent light stability |
CN112175440A (en) * | 2020-10-29 | 2021-01-05 | 纳琳威纳米科技(上海)有限公司 | Anti-solarization yellowing-resistant anti-aging repair coating and preparation method thereof |
US20210206996A1 (en) * | 2017-04-25 | 2021-07-08 | Basf Se | Coating compositions having covalently bound ultraviolet absorbers |
CN113832729A (en) * | 2021-09-15 | 2021-12-24 | 苏州同构科技有限公司 | Washable ultraviolet absorbent and preparation method thereof |
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2022
- 2022-12-02 CN CN202211537254.8A patent/CN115725213A/en active Pending
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KR20200129066A (en) * | 2016-12-16 | 2020-11-17 | 임상택 | Gloss varnish with excellent light stability |
US20210206996A1 (en) * | 2017-04-25 | 2021-07-08 | Basf Se | Coating compositions having covalently bound ultraviolet absorbers |
CN112175440A (en) * | 2020-10-29 | 2021-01-05 | 纳琳威纳米科技(上海)有限公司 | Anti-solarization yellowing-resistant anti-aging repair coating and preparation method thereof |
CN113832729A (en) * | 2021-09-15 | 2021-12-24 | 苏州同构科技有限公司 | Washable ultraviolet absorbent and preparation method thereof |
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