CN101824254A - Organosilicon-modified polyvinyl butyral coil coating - Google Patents
Organosilicon-modified polyvinyl butyral coil coating Download PDFInfo
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- CN101824254A CN101824254A CN 201010167491 CN201010167491A CN101824254A CN 101824254 A CN101824254 A CN 101824254A CN 201010167491 CN201010167491 CN 201010167491 CN 201010167491 A CN201010167491 A CN 201010167491A CN 101824254 A CN101824254 A CN 101824254A
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- Prior art keywords
- polyvinyl butyral
- organosilicon
- coil coating
- modified polyvinyl
- coating
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Abstract
The invention discloses an organosilicon-modified polyvinyl butyral coil coating comprising the following components by mass percentage: 60% to 70% of alcohol solution of polyvinyl butyral, 10% to 20% of phenyl-trimethoxysilane, 10% to 20% of phenyl-methyl-dimethoxysilane, 1% to 8% of distilled water and 0.5% to 1% of phosphoric acid, wherein the organosilicon-modified polyvinyl butyral coil coating is prepared through the sol-gel reaction. The organosilicon-modified polyvinyl butyral coil coating of the invention has the characteristics of high strength, good toughness, low curing temperature and environment friendliness.
Description
Technical field
The present invention relates to technical field of coatings, relate to a kind of coil coating, more particularly, relate to a kind of organosilicon-modified polyvinyl butyral coil coating.
Background technology
Coil coating puts goods on the market as far back as the U.S. the thirties in 20th century, and development after World War II is very fast, independent formation one big coating system from industrial coating.There is the VOC discharging in traditional coil coating, needs hot setting, sacrifices hardness to increase flexible defective.Carried out a large amount of work around these Study of Defects personnel, some achievements have been obtained, a kind of coil coating is disclosed as patent CN200910029798.1, its solidification value is reduced to 180~190 ℃ by original 224~241 ℃, but such solidification value is still than higher, and energy consumption is still bigger.And patent CN200880003471.0 discloses a kind of excellent flexible coil coating that makes up with hardness that shows, but involved solvent all is the compound that toluene and dimethylbenzene etc. contain phenyl ring in this patent, is unfavorable for environmental protection.
Summary of the invention
Technical problem: the objective of the invention is for overcome existing coil coating exist VOC discharging, solidification value higher, sacrifice hardness to increase flexible defective, solve the relevant technologies problem.A kind of organosilicon-modified polyvinyl butyral coil coating is provided.
Technical scheme: in order to achieve the above object, the present invention is by selecting for use polyvinyl butyral acetal as main filmogen, and adds phenyltrimethoxysila,e, phenyl methyl dimethoxy silane, distilled water, phosphoric acid (85%) make novel coiled material coating by sol gel reaction in system.
The technical scheme that technical solution problem of the present invention is adopted is:
A kind of organosilicon-modified polyvinyl butyral coil coating, alcoholic solution by the component polyvinyl butyral acetal is 60~70% by mass percentage, phenyltrimethoxysila,e is 10~20%, phenyl methyl dimethoxy silane is 10~20%, distilled water is 1~8%, and phosphoric acid is 0.5~1% composition.
The alcoholic solution of above-mentioned polyvinyl butyral acetal be solvent and polyvinyl butyral acetal by quality 60:40 proportioning mixed dissolution, wherein said solvent is a dehydrated alcohol.
The preparation of organosilicon-modified polyvinyl butyral coil coating: at first alcoholic solution, phenyltrimethoxysila,e, phenyl methyl dimethoxy silane, the distilled water of polyvinyl butyral acetal are put in the there-necked flask of being furnished with heating unit according to a certain ratio, when treating that system temperature is stabilized in 50 ℃, dropwise drip phosphoric acid and finish until reaction in system, the reaction times is 5 hours.
Beneficial effect: the advantage and the beneficial effect of organosilicon-modified polyvinyl butyral coil coating of the present invention mainly are:
Because the molecular structure of polyvinyl butyral acetal and efficient film-forming properties provide excellent sticking power and snappiness for coating; The existence of phenyltrimethoxysila,e can further increase the snappiness and the weathering resistance of coating; The final sticking power of coating is 0~1 grade, and hardness is 4H, and 120~180 ° of coatings of base material turnover do not ftracture, and is promptly curable under 50~80 ℃; Of paramount importance is not exist in the whole system the poisonous and hazardous organic gas discharging of environment.
Embodiment
Embodiment 1:
This organosilicon-modified polyvinyl butyral coil coating is pressed following charge ratio (quality percentage composition):
The alcoholic solution 65% of polyvinyl butyral acetal;
Distilled water 1%;
Phosphatase 11 %;
Phenyltrimethoxysila,e 15%;
Phenyl methyl dimethoxy silane 18%.
The preparation method; At first put into alcoholic solution, phenyltrimethoxysila,e, phenyl methyl dimethoxy silane, the distilled water of polyvinyl butyral acetal in the there-necked flask of being furnished with heating unit by above proportioning, when treating that system temperature is stabilized in 50 ℃, dropwise drip phosphoric acid and finish until reaction in system, the reaction times is 5 hours.
The present embodiment effect: the final sticking power of coating is 1 grade, and hardness is 4H, and 160 ° of coatings of base material turnover do not ftracture 60 ℃ of curables.
Embodiment 2:
This organosilicon-modified polyvinyl butyral coil coating is pressed following charge ratio (quality percentage composition):
The alcoholic solution 65% of polyvinyl butyral acetal;
Distilled water 4.2%;
Phosphoric acid 0.8%;
Phenyltrimethoxysila,e 20%;
Phenyl methyl dimethoxy silane 10%.
The preparation method is identical with embodiment 1.
The present embodiment effect: the final sticking power of coating is 1 grade, and hardness is 4H, and 120 ° of coatings of base material turnover do not ftracture 70 ℃ of curables.
Embodiment 3:
This organosilicon-modified polyvinyl butyral coil coating is pressed following charge ratio (quality percentage composition):
The alcoholic solution 60% of polyvinyl butyral acetal;
Distilled water 4%;
Phosphatase 11 %;
Phenyltrimethoxysila,e 20%;
Phenyl methyl dimethoxy silane 15%.
The preparation method is identical with embodiment 1.
The present embodiment effect: the final sticking power of coating is 1 grade, and hardness is 4H, and 180 ° of coatings of base material turnover do not ftracture 80 ℃ of curables.
Embodiment 4:
This organosilicon-modified polyvinyl butyral coil coating is pressed following charge ratio (quality percentage composition):
The alcoholic solution 70% of polyvinyl butyral acetal;
Distilled water 1%;
Phosphatase 11 %;
Phenyltrimethoxysila,e 13%;
Phenyl methyl dimethoxy silane 15%.
The preparation method is identical with embodiment 1.
The present embodiment effect: the final sticking power of coating is 0 grade, and hardness is 4H, and 180 ° of coatings of base material turnover do not ftracture 50 ℃ of curables.
Embodiment 5:
This organosilicon-modified polyvinyl butyral coil coating is pressed following charge ratio (quality percentage composition):
The alcoholic solution 65.5% of polyvinyl butyral acetal;
Distilled water 4%;
Phosphoric acid 0.5%;
Phenyltrimethoxysila,e 10%;
Phenyl methyl dimethoxy silane 20%.
The preparation method is identical with embodiment 1.
The present embodiment effect: the final sticking power of coating is 1 grade, and hardness is 4H, and 120 ° of coatings of base material turnover do not ftracture 80 ℃ of curables.
Embodiment 6:
This organosilicon-modified polyvinyl butyral coil coating is pressed following charge ratio (quality percentage composition):
The alcoholic solution 61.5% of polyvinyl butyral acetal;
Distilled water 8%;
Phosphoric acid 0.5%;
Phenyltrimethoxysila,e 20%;
Phenyl methyl dimethoxy silane 10%.
The preparation method is identical with embodiment 1.
The present embodiment effect: the final sticking power of coating is 0 grade, and hardness is 4H, and 150 ° of coatings of base material turnover do not ftracture 70 ℃ of curables.
Claims (3)
1. an organosilicon-modified polyvinyl butyral coil coating is characterized in that, is made up of alcoholic solution, phenyltrimethoxysila,e, phenyl methyl dimethoxy silane, distilled water and the phosphoric acid of polyvinyl butyral acetal; Wherein the mass percent of each component is:
The alcoholic solution 60~70% of polyvinyl butyral acetal;
Phenyltrimethoxysila,e 10~20%;
Phenyl methyl dimethoxy silane 10~20%;
Distilled water 1~8%;
Phosphoric acid 0.5~1%.
2. organosilicon-modified polyvinyl butyral coil coating according to claim 1 is characterized in that, the alcoholic solution of described polyvinyl butyral acetal is solvent and the polyvinyl butyral acetal mixed dissolution thing by 60: 40 proportionings of mass ratio.
3. organosilicon-modified polyvinyl butyral coil coating according to claim 2 is characterized in that, described solvent is a dehydrated alcohol.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CN2010101674910A CN101824254B (en) | 2010-05-10 | 2010-05-10 | Organosilicon-modified polyvinyl butyral coil coating |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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CN2010101674910A CN101824254B (en) | 2010-05-10 | 2010-05-10 | Organosilicon-modified polyvinyl butyral coil coating |
Publications (2)
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CN101824254A true CN101824254A (en) | 2010-09-08 |
CN101824254B CN101824254B (en) | 2012-08-22 |
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CN2010101674910A Expired - Fee Related CN101824254B (en) | 2010-05-10 | 2010-05-10 | Organosilicon-modified polyvinyl butyral coil coating |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102604494A (en) * | 2012-02-27 | 2012-07-25 | 江苏科技大学 | Coating for wind power generation blades |
CN104341888A (en) * | 2013-07-29 | 2015-02-11 | 董思伟 | Organosilicon-polyvinyl butyral coating (called S-PVB for short) with interpenetrating network structure and preparation method thereof |
CN115093744A (en) * | 2022-07-07 | 2022-09-23 | 合肥旭阳铝颜料有限公司 | Mirror silver ink and application thereof in packaging printed matter |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101067067A (en) * | 2007-06-04 | 2007-11-07 | 江阴市大阪涂料有限公司 | Heat resistant paint for iron and steel |
CN101096486A (en) * | 2006-06-29 | 2008-01-02 | 彭文表 | Temperature-resistant rust anticorrosion paint and preparation method thereof |
-
2010
- 2010-05-10 CN CN2010101674910A patent/CN101824254B/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101096486A (en) * | 2006-06-29 | 2008-01-02 | 彭文表 | Temperature-resistant rust anticorrosion paint and preparation method thereof |
CN101067067A (en) * | 2007-06-04 | 2007-11-07 | 江阴市大阪涂料有限公司 | Heat resistant paint for iron and steel |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102604494A (en) * | 2012-02-27 | 2012-07-25 | 江苏科技大学 | Coating for wind power generation blades |
CN102604494B (en) * | 2012-02-27 | 2014-04-16 | 江苏科技大学 | Coating for wind power generation blades |
CN104341888A (en) * | 2013-07-29 | 2015-02-11 | 董思伟 | Organosilicon-polyvinyl butyral coating (called S-PVB for short) with interpenetrating network structure and preparation method thereof |
CN115093744A (en) * | 2022-07-07 | 2022-09-23 | 合肥旭阳铝颜料有限公司 | Mirror silver ink and application thereof in packaging printed matter |
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CN101824254B (en) | 2012-08-22 |
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SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
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CP02 | Change in the address of a patent holder |
Address after: 212028 Zhenjiang, Dantu Metro Industrial Park Rui East Road, No. 9 Patentee after: Jiangsu University of Science and Technology Address before: 212003 Zhenjiang City, Jiangsu province dream Creek Road, No. 2 Patentee before: Jiangsu University of Science and Technology |
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CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20120822 Termination date: 20170510 |