CN105199494B - A kind of fluorocarbon resin coating and preparation method thereof - Google Patents
A kind of fluorocarbon resin coating and preparation method thereof Download PDFInfo
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- CN105199494B CN105199494B CN201510704033.9A CN201510704033A CN105199494B CN 105199494 B CN105199494 B CN 105199494B CN 201510704033 A CN201510704033 A CN 201510704033A CN 105199494 B CN105199494 B CN 105199494B
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- 229920005989 resin Polymers 0.000 title claims abstract description 39
- 239000011347 resin Substances 0.000 title claims abstract description 39
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 title claims abstract description 38
- 238000000576 coating method Methods 0.000 title claims abstract description 30
- 239000011248 coating agent Substances 0.000 title claims abstract description 26
- 238000002360 preparation method Methods 0.000 title claims abstract description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 34
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 21
- 239000005543 nano-size silicon particle Substances 0.000 claims abstract description 4
- 239000003054 catalyst Substances 0.000 claims abstract description 3
- 150000005168 4-hydroxybenzoic acids Chemical class 0.000 claims abstract 3
- 239000002245 particle Substances 0.000 claims description 12
- 239000012046 mixed solvent Substances 0.000 claims description 10
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 8
- 239000002270 dispersing agent Substances 0.000 claims description 8
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims description 5
- 238000003756 stirring Methods 0.000 claims description 5
- 239000003822 epoxy resin Substances 0.000 claims description 4
- 229920000647 polyepoxide Polymers 0.000 claims description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 4
- 239000007983 Tris buffer Substances 0.000 claims description 3
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 claims description 3
- 239000006185 dispersion Substances 0.000 claims description 3
- 239000011259 mixed solution Substances 0.000 claims description 3
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 claims description 3
- 239000011164 primary particle Substances 0.000 claims description 2
- 239000000243 solution Substances 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 239000002518 antifoaming agent Substances 0.000 claims 3
- 238000013019 agitation Methods 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 238000002156 mixing Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 238000002604 ultrasonography Methods 0.000 claims 1
- 238000005406 washing Methods 0.000 claims 1
- 235000012239 silicon dioxide Nutrition 0.000 abstract description 12
- 239000002253 acid Substances 0.000 abstract description 6
- 239000003513 alkali Substances 0.000 abstract description 5
- 238000005260 corrosion Methods 0.000 abstract description 4
- 230000004048 modification Effects 0.000 abstract description 4
- 238000012986 modification Methods 0.000 abstract description 4
- 239000003973 paint Substances 0.000 abstract description 4
- 230000032683 aging Effects 0.000 abstract description 3
- 238000004140 cleaning Methods 0.000 abstract description 3
- 230000007797 corrosion Effects 0.000 abstract description 3
- 230000002209 hydrophobic effect Effects 0.000 abstract description 3
- 238000000034 method Methods 0.000 abstract description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 2
- 239000003960 organic solvent Substances 0.000 abstract description 2
- 239000002131 composite material Substances 0.000 abstract 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 13
- 229910052681 coesite Inorganic materials 0.000 description 10
- 229910052906 cristobalite Inorganic materials 0.000 description 10
- 229910052682 stishovite Inorganic materials 0.000 description 10
- 229910052905 tridymite Inorganic materials 0.000 description 10
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 description 6
- 229910004298 SiO 2 Inorganic materials 0.000 description 5
- 239000008096 xylene Substances 0.000 description 3
- YXRKNIZYMIXSAD-UHFFFAOYSA-N 1,6-diisocyanatohexane Chemical compound O=C=NCCCCCCN=C=O.O=C=NCCCCCCN=C=O.O=C=NCCCCCCN=C=O YXRKNIZYMIXSAD-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000013530 defoamer Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000009776 industrial production Methods 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002715 modification method Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
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Abstract
Description
技术领域technical field
本发明涉及一种建筑涂料及其制备方法,特别是涉及一种氟碳树脂涂料及其制备方法。The invention relates to an architectural coating and a preparation method thereof, in particular to a fluorocarbon resin coating and a preparation method thereof.
背景技术Background technique
氟碳树脂以牢固的C-F键为骨架,同其他树脂相比,其耐热性、耐化学品性、耐寒性、低温柔韧性、耐候性和电性能等均较好。但是由于氟碳树脂的 C-F 键的健长短和键能大的原因导致其结晶性良好,故其同时也具有不粘附性和不湿润性的缺点。由上述可知如果直接将氟碳树脂用于涂料中,虽然涂料短时间内具有良好的保护性能,但是由于其不粘附和不湿润的特性会导致涂料很容易就会脱落,从而对基体不再具有保护作用,这就违反了使用涂料的初衷。Fluorocarbon resin has a strong C-F bond as the skeleton. Compared with other resins, it has better heat resistance, chemical resistance, cold resistance, low temperature flexibility, weather resistance and electrical properties. However, due to the short length and high bond energy of the C-F bond of fluorocarbon resin, it has good crystallinity, so it also has the disadvantages of non-adhesion and non-wetting. It can be seen from the above that if the fluorocarbon resin is directly used in the coating, although the coating has good protective performance in a short period of time, due to its non-adhesive and non-wetting characteristics, the coating will easily fall off, thus no longer affecting the substrate. It has a protective effect, which violates the original intention of using paint.
纳米SiO2虽然能较好的改善氟碳树脂涂料存在的缺点,但是纳米SiO2粒子的表面原子具有很高的活性,极不稳定,极易团聚,在氟碳涂料中分散性很差。因此必须对纳米SiO2的表面进行改性,使其能够较好且均匀的分散在氟碳树脂涂料中。传统的纳米SiO2改性方法对条件要求极为苛刻,其中一些高温,高压,强酸、强碱、高额偶联剂等方法致使其在改性时成本升高,不利于工业化生产。Although nano-SiO 2 can better improve the shortcomings of fluorocarbon resin coatings, the surface atoms of nano-SiO 2 particles are highly active, extremely unstable, and easy to agglomerate, and their dispersion in fluorocarbon coatings is poor. Therefore, the surface of nano- SiO2 must be modified so that it can be better and uniformly dispersed in the fluorocarbon resin coating. Traditional nano-SiO 2 modification methods are extremely demanding on conditions, and some methods such as high temperature, high pressure, strong acid, strong alkali, and high-cost coupling agent increase the cost of modification, which is not conducive to industrial production.
发明内容Contents of the invention
本发明的目的在于提供一种氟碳树脂涂料及其制备方法,本发明以纳米SiO2改性的氟碳树脂涂料,既能保持氟碳树脂原有的优异性能,又能获取优异的力学性能、热稳定性和其他性能,而且又具有较强的耐腐蚀性、抗紫外老化性、耐酸碱性、疏水自清洁性能和耐热耐候性。The object of the present invention is to provide a kind of fluorocarbon resin coating and preparation method thereof, the present invention is with nanometer SiO 2 Modified fluorocarbon resin coating, both can keep the original excellent performance of fluorocarbon resin, can obtain excellent mechanical property again , thermal stability and other properties, but also has strong corrosion resistance, UV aging resistance, acid and alkali resistance, hydrophobic self-cleaning performance and heat and weather resistance.
本发明的目的是通过以下技术方案实现的:The purpose of the present invention is achieved through the following technical solutions:
一种氟碳树脂涂料,该涂料质量百分比组成如下:A kind of fluorocarbon resin paint, this paint mass percentage is composed as follows:
氟碳树脂30%-40%;环氧树脂5%-10%;p-羟基苯甲酸5%-10%;溶剂30%-40%;流平剂0.5%-1%;消泡剂 0.5%-2%;纳米二氧化硅5%-8%;分散剂2%-5%;催化剂1.5%-5%。Fluorocarbon resin 30%-40%; epoxy resin 5%-10%; p-hydroxybenzoic acid 5%-10%; solvent 30%-40%; leveling agent 0.5%-1%; defoamer 0.5% -2%; nano-silica 5%-8%; dispersant 2%-5%; catalyst 1.5%-5%.
所述的一种氟碳树脂涂料,所用的氟碳树脂为三氟型 FEVE 氟碳树脂。The fluorocarbon resin coating described above is a trifluoro-type FEVE fluorocarbon resin.
所述的一种氟碳树脂涂料,所用的纳米二氧化硅粒子的一次粒径为25-30nm。In the above-mentioned fluorocarbon resin coating, the primary particle diameter of the nano silicon dioxide particles used is 25-30nm.
所述的一种氟碳树脂涂料,混合溶剂中二甲苯和乙二醇丁醚的体积比为2:3~4。In the fluorocarbon resin coating, the volume ratio of xylene and ethylene glycol butyl ether in the mixed solvent is 2:3~4.
所述的一种氟碳树脂涂料,所用的流平剂为MF3077、RB505、SC-333。For the fluorocarbon resin coating, the leveling agents used are MF3077, RB505, and SC-333.
所述的一种氟碳树脂涂料,所用的消泡剂为GPE20、SPA -202。For the fluorocarbon resin coating, the defoamers used are GPE20 and SPA-202.
所述的一种氟碳树脂涂料,所用的分散剂为多组分分散剂,其组成为HDI 三聚体HX 和 HDI 缩二脲 N75,且二者的百分比为10:7~8。For the fluorocarbon resin coating, the dispersant used is a multi-component dispersant, which consists of HDI trimer HX and HDI biuret N75, and the percentage of the two is 10:7~8.
一种氟碳树脂涂料的制备方法,包括以下制备步骤:A preparation method of fluorocarbon resin coating, comprising the following preparation steps:
a将5%-8%的纳米SiO2粒子加入到5%-10%的由二甲苯和乙二醇丁醚组成的混合溶剂中,用Tris缓冲液调节PH至8-9,然后加入5%-10%的p-羟基苯甲酸和1.5%-5%的吡啶,搅拌2h,抽滤、洗涤,再在120℃-200℃下干燥得到改性后的纳米SiO2粒子;a Add 5%-8% of nano- SiO2 particles to 5%-10% of a mixed solvent composed of xylene and ethylene glycol butyl ether, adjust the pH to 8-9 with Tris buffer, and then add 5% -10% of p-hydroxybenzoic acid and 1.5%-5% of pyridine, stirred for 2h, suction filtered, washed, and then dried at 120°C-200°C to obtain modified nano- SiO2 particles;
b将30%-40%氟碳树脂和5%-10%环氧树脂倒入三口烧瓶中,然后加入25%-30%的混合溶剂,超声0.5-1.0h,恒温40 ℃,将5%-8%的改性纳米SiO2粒子添加到3%-5%的混合溶剂中,超声分散15-30 min,将得到的混合溶液缓慢滴入三口烧瓶中,机械搅拌0.5-1.0h后再超声1-2 h;b Pour 30%-40% fluorocarbon resin and 5%-10% epoxy resin into a three-necked flask, then add 25%-30% mixed solvent, ultrasonic 0.5-1.0h, constant temperature 40 ℃, 5%- Add 8% modified nano- SiO2 particles to 3%-5% mixed solvent, ultrasonically disperse for 15-30 min, slowly drop the obtained mixed solution into a three-necked flask, mechanically stir for 0.5-1.0h, and then ultrasonically 1 -2 h;
c将0.5%-1%的流平剂和0.5%-2%的消泡剂加入到改性氟碳树脂中,机械搅拌1-2h分散均匀,加入2%-5%的分散剂,再高速分散 5-30 min,从而制得涂料。c Add 0.5%-1% leveling agent and 0.5%-2% defoamer to the modified fluorocarbon resin, mechanically stir for 1-2h to disperse evenly, add 2%-5% dispersant, and then high-speed Disperse for 5-30 min to prepare the coating.
本发明的优点与效果是:Advantage and effect of the present invention are:
1.以纳米SiO2改性的氟碳树脂涂料,既能保持氟碳树脂原有的优异性能,又能获取优异的力学性能、热稳定性和其他性能,而且又具有较强的耐腐蚀性、抗紫外老化性、耐酸碱性、疏水自清洁性能和耐热耐候性。1. Fluorocarbon resin coatings modified with nano- SiO2 can not only maintain the original excellent properties of fluorocarbon resins, but also obtain excellent mechanical properties, thermal stability and other properties, and have strong corrosion resistance and anti-corrosion properties. UV aging resistance, acid and alkali resistance, hydrophobic self-cleaning performance and heat and weather resistance.
2.采用p-羟基苯甲酸对纳米SiO2表面改性处理,利用二氧化硅表面羟基与p-羟基苯甲酸表面的羧基进行反应,从而对纳米二氧化硅表面的亲水性基团进行改性,使得纳米二氧化硅能较好的分散在有机溶剂中,反应条件较为平和,克服了以往二氧化硅改性需要高温、高压、强酸、强碱的条件的弊端,也避免了使用硅烷偶联剂易造成副作用的缺点。2. Use p-hydroxybenzoic acid to modify the surface of nano- SiO2 , and use the hydroxyl group on the surface of silica to react with the carboxyl group on the surface of p-hydroxybenzoic acid, thereby modifying the hydrophilic groups on the surface of nano-silica, The nano-silica can be better dispersed in organic solvents, and the reaction conditions are relatively mild, which overcomes the disadvantages of high temperature, high pressure, strong acid, and strong alkali conditions required for silica modification in the past, and also avoids the use of silane coupling agents. Easy to cause side effects.
3.本发明利用纳米SiO2对氟碳树脂进行改性不仅克服了传统氟碳树脂涂料的缺点,而且也获得了优异的力学性能和热稳定性,同时采用p-羟基苯甲酸对纳米SiO2表面改性处理,操作简单,反应条件易于控制,可重复性较高,减少了生产成本,易于实现工业化生产。3. The present invention not only overcomes the shortcomings of traditional fluorocarbon resin coatings by using nano-SiO2 to modify fluorocarbon resin, but also obtains excellent mechanical properties and thermal stability, and simultaneously uses p-hydroxybenzoic acid to modify the surface of nano- SiO2 The processing and operation are simple, the reaction conditions are easy to control, the repeatability is high, the production cost is reduced, and industrial production is easy to realize.
附图说明Description of drawings
图1 p-羟基苯甲酸在吡啶催化下合成聚酯的机理图;Fig. 1 The schematic diagram of the synthesis of polyester from p-hydroxybenzoic acid under the catalysis of pyridine;
图2聚酯改性纳米二氧化硅的机理图。Fig. 2 Mechanism diagram of polyester modified nano-silica.
具体实施方式Detailed ways
下面通过实施案例进一步详细描述本发明的实施方案,但发明的实施方式不局限于此。Embodiments of the present invention will be further described in detail through examples below, but the embodiments of the invention are not limited thereto.
a.将5%的纳米SiO2粒子加入到5%的二甲苯和乙二醇丁醚配体积比为2:3的混合溶剂中,用Tris缓冲液调节PH=9,然后加入8%的p-羟基苯甲酸和5%的吡啶,搅拌2h,抽滤、洗涤,再在150℃下干燥得到改性后的纳米SiO2粒子。a. Add 5% nano- SiO2 particles to 5% xylene and ethylene glycol butyl ether in a mixed solvent with a volume ratio of 2:3, adjust the pH to 9 with Tris buffer, and then add 8% p-hydroxyl Benzoic acid and 5% pyridine were stirred for 2 hours, filtered with suction, washed, and dried at 150°C to obtain modified nano-SiO 2 particles.
b.将35%的三氟型FEVE氟碳树脂和10%的环氧树脂倒入三口烧瓶中,然后加入30%的上述混合溶剂;超声1.0h,恒温40 ℃。将5%的改性纳米SiO2粒子添加到5%的上述混合溶剂中;超声分散 30 min,将所得到的混合溶液缓慢滴入三口烧瓶中,机械搅拌1.0,超声2h。b. Pour 35% of trifluoro-type FEVE fluorocarbon resin and 10% of epoxy resin into a three-necked flask, and then add 30% of the above mixed solvent; ultrasonic 1.0h, constant temperature 40 ℃. Add 5% of modified nano- SiO2 particles to 5% of the above mixed solvent; ultrasonically disperse for 30 min, slowly drop the resulting mixed solution into a three-necked flask, mechanically stir for 1.0, and ultrasonically for 2h.
c.将1%的MF3077和2%的GPE20加入到改性氟碳树脂中,机械搅拌2h分散均匀;加入体积百分比为10:7的HDI三聚体HX 和HDI缩二脲 N75,高速分散 20 min,从而制得涂料。c. Add 1% of MF3077 and 2% of GPE20 to the modified fluorocarbon resin, stir mechanically for 2 hours to disperse evenly; add HDI trimer HX and HDI biuret N75 with a volume percentage of 10:7, and disperse at high speed for 20 minutes. Thus, a coating is produced.
以上仅是本发明的较佳实施,并非对本发明做任何形式上的限制,凡是依据本发明的技术实质,对以上实施方案所做的任何简单修改、等同变化,均落入本发明的保护范围。The above are only preferred implementations of the present invention, and are not intended to limit the present invention in any form. Any simple modifications or equivalent changes made to the above embodiments according to the technical essence of the present invention all fall within the scope of protection of the present invention. .
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102002289A (en) * | 2010-12-15 | 2011-04-06 | 广东电网公司电力科学研究院 | Normal temperature curing fluorocarbon resin coating and preparation method thereof |
CN103131275A (en) * | 2012-12-06 | 2013-06-05 | 常州大学 | Nano silicon dioxide (SiO2) improved fluorocarbon coating and preparation thereof |
CN103709854A (en) * | 2013-12-31 | 2014-04-09 | 上海交通大学 | Water dispersible fluorocarbon finish coating and preparation method thereof |
CN103865371A (en) * | 2014-03-17 | 2014-06-18 | 常州大学 | Preparation method of modified trifluoro-FEVE (Fluorinated Ethylene Vinyl Ether) fluorocarbon coating |
CN103965669A (en) * | 2013-01-29 | 2014-08-06 | 惠州市华昱美实业有限公司 | Waterborne fluorocarbon paint |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102002289A (en) * | 2010-12-15 | 2011-04-06 | 广东电网公司电力科学研究院 | Normal temperature curing fluorocarbon resin coating and preparation method thereof |
CN103131275A (en) * | 2012-12-06 | 2013-06-05 | 常州大学 | Nano silicon dioxide (SiO2) improved fluorocarbon coating and preparation thereof |
CN103965669A (en) * | 2013-01-29 | 2014-08-06 | 惠州市华昱美实业有限公司 | Waterborne fluorocarbon paint |
CN103709854A (en) * | 2013-12-31 | 2014-04-09 | 上海交通大学 | Water dispersible fluorocarbon finish coating and preparation method thereof |
CN103865371A (en) * | 2014-03-17 | 2014-06-18 | 常州大学 | Preparation method of modified trifluoro-FEVE (Fluorinated Ethylene Vinyl Ether) fluorocarbon coating |
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