CN114656869B - Wind power tower finish paint containing indium chloride coated carbon nanofibers and preparation method and use method thereof - Google Patents
Wind power tower finish paint containing indium chloride coated carbon nanofibers and preparation method and use method thereof Download PDFInfo
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- PSCMQHVBLHHWTO-UHFFFAOYSA-K indium(iii) chloride Chemical compound Cl[In](Cl)Cl PSCMQHVBLHHWTO-UHFFFAOYSA-K 0.000 title claims abstract description 46
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 title claims abstract description 25
- 239000002134 carbon nanofiber Substances 0.000 title claims abstract description 24
- 238000002360 preparation method Methods 0.000 title claims abstract description 13
- 238000000034 method Methods 0.000 title claims abstract description 9
- 239000003973 paint Substances 0.000 title abstract description 18
- 229920000049 Carbon (fiber) Polymers 0.000 claims abstract description 28
- 239000004917 carbon fiber Substances 0.000 claims abstract description 28
- 229910021392 nanocarbon Inorganic materials 0.000 claims abstract description 24
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 12
- 238000000576 coating method Methods 0.000 claims abstract description 12
- 239000011248 coating agent Substances 0.000 claims abstract description 10
- 238000005240 physical vapour deposition Methods 0.000 claims abstract description 4
- 239000002994 raw material Substances 0.000 claims abstract description 3
- 238000003756 stirring Methods 0.000 claims description 37
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical group CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims description 24
- 239000004611 light stabiliser Substances 0.000 claims description 23
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 20
- 239000006096 absorbing agent Substances 0.000 claims description 14
- 150000001412 amines Chemical class 0.000 claims description 14
- KTFFTVGPHKWIOK-UHFFFAOYSA-N oxalate;phenylazanium Chemical group OC(=O)C(O)=O.NC1=CC=CC=C1.NC1=CC=CC=C1 KTFFTVGPHKWIOK-UHFFFAOYSA-N 0.000 claims description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 13
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 12
- 229920000570 polyether Polymers 0.000 claims description 12
- 229920005862 polyol Polymers 0.000 claims description 12
- 150000003077 polyols Chemical class 0.000 claims description 12
- 229910021485 fumed silica Inorganic materials 0.000 claims description 10
- 229920005989 resin Polymers 0.000 claims description 10
- 239000011347 resin Substances 0.000 claims description 10
- 239000000080 wetting agent Substances 0.000 claims description 9
- 239000002270 dispersing agent Substances 0.000 claims description 7
- 230000001680 brushing effect Effects 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 229920005749 polyurethane resin Polymers 0.000 claims description 2
- 238000007761 roller coating Methods 0.000 claims description 2
- ZIWRUEGECALFST-UHFFFAOYSA-M sodium 4-(4-dodecoxysulfonylphenoxy)benzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCOS(=O)(=O)c1ccc(Oc2ccc(cc2)S([O-])(=O)=O)cc1 ZIWRUEGECALFST-UHFFFAOYSA-M 0.000 claims description 2
- 238000005507 spraying Methods 0.000 claims description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims 1
- 230000003628 erosive effect Effects 0.000 abstract description 9
- 238000005260 corrosion Methods 0.000 abstract description 7
- 230000007797 corrosion Effects 0.000 abstract description 5
- 239000002519 antifouling agent Substances 0.000 abstract description 2
- 230000007423 decrease Effects 0.000 abstract description 2
- 239000000835 fiber Substances 0.000 abstract description 2
- 239000002002 slurry Substances 0.000 description 15
- 150000001252 acrylic acid derivatives Chemical group 0.000 description 11
- 239000003153 chemical reaction reagent Substances 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 10
- 229920002635 polyurethane Polymers 0.000 description 10
- 239000004814 polyurethane Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 6
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- 235000012239 silicon dioxide Nutrition 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 3
- 230000000694 effects Effects 0.000 description 2
- 239000012745 toughening agent Substances 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000009916 joint effect Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
- C09D7/62—Additives non-macromolecular inorganic modified by treatment with other compounds
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/63—Additives non-macromolecular organic
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/70—Additives characterised by shape, e.g. fibres, flakes or microspheres
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/70—Wind energy
- Y02E10/72—Wind turbines with rotation axis in wind direction
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
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- Materials Engineering (AREA)
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- Paints Or Removers (AREA)
Abstract
本发明公开了一种含氯化铟包覆纳米碳纤维的风电塔架面漆及其制备方法和使用方法,属于海上风电防腐剂抗冲蚀技术领域。在传统面漆涂层的基础上,基于纤维增韧机理添加了高韧纳米碳纤维,不仅提升了面漆的强韧性,还显著提升了漆层的耐冲蚀性能,相对传统防护漆层更适用于海洋风电机组的抗冲蚀防护。进一步地,纳米碳纤维通过物理气相沉积法在表面包覆不导电氯化铟,避免了由于导电碳纤维的加入使得漆层耐蚀性能的下降。本发明的制备方法简便、原料易得,制备的面层漆膜具有高韧性、高附着力、耐冲蚀、耐腐蚀的特点,能够显著延长风电塔架飞溅区等海浪冲击环境中漆层的安全服役寿命。The invention discloses a wind power tower topcoat containing indium chloride-coated nano-carbon fibers, a preparation method and a use method thereof, and belongs to the technical field of anti-erosion anti-corrosion agents for offshore wind power. On the basis of the traditional topcoat coating, high-toughness nano-carbon fibers are added based on the fiber toughening mechanism, which not only improves the strength and toughness of the topcoat, but also significantly improves the erosion resistance of the paint layer, which is more suitable than traditional protective paint layers Anti-erosion protection for offshore wind turbines. Furthermore, the carbon nanofibers are coated with non-conductive indium chloride on the surface by physical vapor deposition, which avoids the decline of the corrosion resistance of the paint layer due to the addition of conductive carbon fibers. The preparation method of the present invention is simple and easy to obtain raw materials, and the prepared surface paint film has the characteristics of high toughness, high adhesion, erosion resistance, and corrosion resistance, and can significantly prolong the durability of the paint layer in the environment where waves impact such as wind power tower splash zones. safe service life.
Description
技术领域technical field
本发明属于海上风电抗冲蚀防护技术领域,具体涉及一种含氯化铟包覆纳米碳纤维的风电塔架面漆及其制备方法和使用方法。The invention belongs to the technical field of offshore wind power anti-erosion protection, and in particular relates to a wind power tower topcoat containing indium chloride-coated nano-carbon fibers and a preparation method and application method thereof.
背景技术Background technique
海风具有丰富、稳定、发电效率高等优势,但是由于海洋大气盐分含量高、湿度大,对海上风电机组的抗冲蚀性能提出了极高的要求。海上风电机组服役环境主要分为五种:大气区、飞溅区、潮差区、全浸区、海泥区。飞溅区一般指高出海平面0-2米的区域,为海浪飞溅可及但海水涨潮时不会被海水淹没的区域。飞溅区除了受海洋大气区腐蚀环境的影响,还受到飞溅海浪的浸湿和冲击,干湿交替频繁,是最容易由于冲蚀导致涂层剥落失效的区域。Sea breeze has the advantages of abundance, stability, and high power generation efficiency. However, due to the high salt content and high humidity in the ocean atmosphere, extremely high requirements are placed on the erosion resistance of offshore wind turbines. The service environment of offshore wind turbines is mainly divided into five types: atmospheric area, splash area, tidal range area, full immersion area, and sea mud area. The splash zone generally refers to the area 0-2 meters above the sea level, which is an area that can be splashed by waves but will not be submerged by sea water when the sea tide is high. In addition to being affected by the corrosive environment of the marine atmosphere, the splash zone is also soaked and impacted by the splash waves, and the alternating wet and dry is frequent, which is the area most likely to cause the coating to peel off and fail due to erosion.
目前,海上风电机组主要依靠树脂等高分子涂层,部分辅助牺牲阳极的方式实现抗冲蚀防护,进而达到延长海上风电机组服役寿命的目的。传统树脂为主的高分子涂层虽然具有良好的柔韧性和耐腐蚀性,但其自身特征使得其耐冲蚀性能较低。特别地,树脂为主的高分子涂层在飞溅区等海洋环境下由于海浪冲击等恶劣环境的影响,极易出现开裂、剥落等问题,极大降低了涂层防护效果和服役寿命,加大了还是风电机组抗冲蚀防护的成本。At present, offshore wind turbines mainly rely on polymer coatings such as resins, and partially assist sacrificial anodes to achieve anti-erosion protection, thereby achieving the purpose of prolonging the service life of offshore wind turbines. Although the traditional resin-based polymer coating has good flexibility and corrosion resistance, its own characteristics make its erosion resistance low. In particular, resin-based polymer coatings are prone to problems such as cracking and peeling in marine environments such as splash zones due to the impact of waves and other harsh environments, which greatly reduces the protective effect and service life of the coating, and increases the It is still the cost of anti-erosion protection for wind turbines.
发明内容Contents of the invention
为了解决上述问题,本发明公开了一种含氯化铟包覆纳米碳纤维的风电塔架面漆及其制备方法和使用方法,制备的面层漆膜具有高韧性、高附着力、耐冲蚀、耐腐蚀的特点,能够显著延长风电塔架飞溅区等海浪冲击环境中漆层的安全服役寿命。In order to solve the above problems, the present invention discloses a wind power tower topcoat containing indium chloride coated nano-carbon fiber and its preparation method and application method. The prepared topcoat paint film has high toughness, high adhesion, and erosion resistance , Corrosion resistance, can significantly prolong the safe service life of the paint layer in the wave impact environment such as wind power tower splash zone.
本发明是通过以下技术方案来实现:The present invention is achieved through the following technical solutions:
本发明公开了一种含氯化铟包覆纳米碳纤维的风电塔架面漆,以质量份数计,包含以下原料:The invention discloses a wind power tower topcoat containing indium chloride coated nano-carbon fiber, which comprises the following raw materials in parts by mass:
树脂50-60份、分散剂3-5份、气相二氧化硅5-7份、流平剂2-3份、催干剂2-3份、光稳定剂2-4份、氯化铟包覆纳米碳纤维5-15份、增润剂0.5-2份和邻苯甲酰磺酰亚胺0.1-1份。50-60 parts of resin, 3-5 parts of dispersant, 5-7 parts of fumed silica, 2-3 parts of leveling agent, 2-3 parts of drier, 2-4 parts of light stabilizer, indium chloride package Covering 5-15 parts of nano-carbon fiber, 0.5-2 parts of wetting agent and 0.1-1 part of o-benzoylsulfonimide.
优选地,树脂为聚氨酯树脂,分散剂为丙烯酸酯,流平剂为氟改性丙烯酸酯,催干剂为有机锡催干剂T-12,光稳定剂为苯胺乙二酸光吸收剂与受阻胺光稳定剂的复合物,增润剂为邻苯二甲酸二丁酯或十二烷基二苯醚二磺酸钠。Preferably, the resin is polyurethane resin, the dispersant is acrylate, the leveling agent is fluorine-modified acrylate, the drier is organotin drier T-12, and the light stabilizer is aniline oxalic acid light absorber and hindered Compound of amine light stabilizer, wetting agent is dibutyl phthalate or sodium dodecyl diphenyl ether disulfonate.
进一步优选地,光稳定剂中,苯胺乙二酸光吸收剂与受阻胺光稳定剂的质量比为1:1。Further preferably, in the light stabilizer, the mass ratio of the aniline oxalic acid light absorber to the hindered amine light stabilizer is 1:1.
优选地,氯化铟包覆纳米碳纤维的直径为100~700nm,长度为10~30μm。Preferably, the indium chloride-coated carbon nanofibers have a diameter of 100-700 nm and a length of 10-30 μm.
优选地,氯化铟包覆纳米碳纤维是通过物理气相沉积法将氯化铟包覆于纳米碳纤维而制得的。Preferably, the carbon nanofiber coated with indium chloride is prepared by coating the carbon nanofiber with indium chloride by physical vapor deposition.
本发明公开了一种含氯化铟包覆纳米碳纤维的风电塔架面漆的制备方法,包括以下步骤:The invention discloses a preparation method of a wind power tower topcoat containing indium chloride coated nano-carbon fiber, which comprises the following steps:
将50-60份树脂、5-15份氯化铟包覆纳米碳纤维、0.5-2份增润剂、3-5份分散剂和5-7份气相二氧化硅充分搅拌均匀;Fully stir 50-60 parts of resin, 5-15 parts of indium chloride-coated carbon nanofibers, 0.5-2 parts of wetting agent, 3-5 parts of dispersant and 5-7 parts of fumed silica;
步骤2:在步骤1得到的混合体系基础上,边搅拌边加入2-3份流平剂、2-3份催干剂、0.1-1份邻苯甲酰磺酰亚胺和2-4份光稳定剂,充分搅拌至完全均匀分散,静置消泡后得到含氯化铟包覆纳米碳纤维的风电塔架面漆;Step 2: On the basis of the mixed system obtained in step 1, add 2-3 parts of leveling agent, 2-3 parts of drier, 0.1-1 part of o-benzoylsulfonimide and 2-4 parts of The light stabilizer is fully stirred until it is completely uniformly dispersed, and after standing for defoaming, a wind power tower topcoat containing indium chloride-coated carbon nanofibers is obtained;
上述用量份数均为质量份数。The above-mentioned dosage parts are all parts by mass.
优选地,步骤1中,搅拌的速度为550-600rpm,时间为20-35min。Preferably, in step 1, the stirring speed is 550-600rpm, and the stirring time is 20-35min.
优选地,步骤2中,搅拌的速度为550-600rpm,所有组分加入完毕后,继续搅拌10-25分钟。Preferably, in step 2, the stirring speed is 550-600 rpm, and after all the components are added, the stirring is continued for 10-25 minutes.
本发明公开了上述制备方法制得的含氯化铟包覆纳米碳纤维的风电塔架面漆的使用方法,制得的含氯化铟包覆纳米碳纤维的风电塔架面漆在使用时,加入30-40份聚醚多元醇作为固化剂,混合均匀后加入稀释剂调节至所需粘度,通过喷涂、辊涂或刷涂均匀涂装至工件表面。The invention discloses a method for using the wind power tower topcoat containing indium chloride coated nano-carbon fibers prepared by the above preparation method. When the prepared wind power tower top paint containing indium chloride coated nano-carbon fibers is used, add 30-40 parts of polyether polyol is used as curing agent, after mixing evenly, add diluent to adjust to the required viscosity, and evenly coat the surface of the workpiece by spraying, roller coating or brushing.
优选地,涂装后的面漆涂层的干膜厚度为100~150μm。Preferably, the dry film thickness of the topcoat after painting is 100-150 μm.
与现有技术相比,本发明具有以下有益的技术效果:Compared with the prior art, the present invention has the following beneficial technical effects:
本发明公开的含氯化铟包覆纳米碳纤维的风电塔架面漆,在传统面漆涂层的基础上,基于纤维增韧机理添加了高韧纳米碳纤维,不仅可以提升面漆的强韧性,还能显著提升漆层的耐冲蚀性能,相对传统防护漆层更适用于海洋风电机组的抗冲蚀防护。进一步地,本发明通过物理气相沉积的方法在碳纤维表面包覆了一层不导电氯化铟,避免了由于导电碳纤维的加入使得漆层耐蚀性能的下降。同时,本发明通过添加增润剂,提高了纳米碳纤维与基体间的结合力,确保了增韧剂优异性能的实现。最后,面漆中通过加入去应力剂邻苯甲酰磺酰亚胺,解决了由于纳米碳纤维添加可能导致漆膜应力增加的问题。因此,在不导电氯化铟包覆纳米碳纤维增韧剂、增润剂以及去应力剂等的共同作用下,制备得到的面漆具有优异的强韧性、高附着力、耐冲蚀、抗磨损的特点,能够在飞溅区等恶劣海洋环境下发挥优异的抗冲蚀防护效果。The wind power tower topcoat containing indium chloride coated nano-carbon fiber disclosed by the present invention, on the basis of traditional topcoat coating, adds high-toughness nano-carbon fiber based on the fiber toughening mechanism, which can not only improve the strength and toughness of the topcoat, It can also significantly improve the erosion resistance of the paint layer, which is more suitable for the erosion protection of offshore wind turbines compared with traditional protective paint layers. Furthermore, the present invention coats a layer of non-conductive indium chloride on the surface of carbon fibers by means of physical vapor deposition, which avoids the decline in the corrosion resistance of the paint layer due to the addition of conductive carbon fibers. At the same time, the present invention improves the binding force between the carbon nanofiber and the matrix by adding a wetting agent, ensuring the realization of the excellent performance of the toughening agent. Finally, the stress-relief agent o-benzoylsulfonimide is added to the topcoat to solve the problem that the stress of the paint film may be increased due to the addition of carbon nanofibers. Therefore, under the joint action of non-conductive indium chloride-coated nano-carbon fiber toughener, wetting agent and stress-relief agent, the prepared topcoat has excellent toughness, high adhesion, erosion resistance and wear resistance. It can exert excellent anti-erosion protection effect in harsh marine environments such as splash zones.
本发明公开的上述含氯化铟包覆纳米碳纤维的风电塔架面漆的制备方法及使用方法,操作简便,便于现场进行使用。The preparation method and application method of the above-mentioned wind power tower topcoat containing indium chloride coated nano-carbon fiber disclosed by the present invention are easy to operate and convenient for on-site use.
具体实施方式Detailed ways
下面结合具体的实施例对本发明做进一步的详细说明,所述是对本发明的解释而不是限定。如无特殊说明,实施例中涉及份数的,均以质量份数计。The present invention will be further described in detail below in conjunction with specific embodiments, which are explanations of the present invention rather than limitations. Unless otherwise specified, all references to parts in the embodiments are in parts by mass.
实施例1Example 1
本实施例漆膜组份:聚氨酯50份;氯化铟包覆纳米碳纤维5份;丙烯酸酯3份;气相二氧化硅5份;氟改性丙烯酸酯2份;T-12有机锡催干剂2份;苯胺乙二酸光吸收剂与受阻胺光稳定剂复合物(按质量比1:1复合)2份;邻苯二甲酸二丁酯0.5份;邻苯甲酰磺酰亚胺0.1份;聚醚多元醇30份。Components of the paint film in this example: 50 parts of polyurethane; 5 parts of carbon nanofiber coated with indium chloride; 3 parts of acrylate; 5 parts of fumed silica; 2 parts of fluorine-modified acrylate; T-12 organotin drier 2 parts; 2 parts of the complex of aniline oxalic acid light absorber and hindered amine light stabilizer (1:1 by mass ratio); 0.5 parts of dibutyl phthalate; 0.1 part of o-benzoylsulfonimide ; 30 parts of polyether polyols.
步骤1:将50份聚氨酯加入干净的容器中,以600rpm的搅拌速度边搅拌边加5份氯化铟包覆纳米碳纤维、0.5份邻苯二甲酸二丁酯、3份丙烯酸酯、5份气相二氧化硅,待所有试剂加入后以600rpm的搅拌速度继续搅拌20分钟;Step 1: Add 50 parts of polyurethane to a clean container, and add 5 parts of indium chloride-coated carbon nanofibers, 0.5 parts of dibutyl phthalate, 3 parts of acrylate, and 5 parts of gas phase while stirring at a stirring speed of 600 rpm Silicon dioxide, after all the reagents are added, continue to stir for 20 minutes at a stirring speed of 600rpm;
步骤2:在步骤1的浆料中以550rpm的搅拌速度边搅拌边加入2份氟改性丙烯酸酯、2份有机锡催干剂T-12、0.1份邻苯甲酰磺酰亚胺、2份苯胺乙二酸光吸收剂与受阻胺光稳定剂复合物。全部试剂加入后以550rpm的搅拌速度继续搅拌20min,静置至气泡完全消失;Step 2: Add 2 parts of fluorine-modified acrylate, 2 parts of organotin drier T-12, 0.1 part of o-benzoylsulfonimide, 2 parts of A compound of aniline oxalic acid light absorber and hindered amine light stabilizer. After adding all the reagents, continue to stir at a stirring speed of 550rpm for 20min, and let stand until the bubbles completely disappear;
步骤3:在步骤2制备的浆料中,加入30份聚醚多元醇,混合均匀,然后将浆料调节至合适黏度。Step 3: Add 30 parts of polyether polyol to the slurry prepared in step 2, mix well, and then adjust the slurry to a suitable viscosity.
步骤4:将步骤3中的浆料喷涂于低碳钢板上。Step 4: Spray the slurry in step 3 on the low carbon steel plate.
步骤5:将步骤4的试件在室温下静置、晾干,各项技术指标结果见表1。Step 5: Let the test piece of step 4 stand at room temperature and dry, and the results of various technical indicators are shown in Table 1.
实施例2Example 2
本实施例漆膜组份:聚氨酯53份;氯化铟包覆纳米碳纤维10份;丙烯酸酯4份;气相二氧化硅6份;氟改性丙烯酸酯2.5份;T-12有机锡催干剂3份;苯胺乙二酸光吸收剂与受阻胺光稳定剂复合物(按质量比1:1复合)3份;邻苯二甲酸二丁酯1份;邻苯甲酰磺酰亚胺0.6份;聚醚多元醇35份。Components of the paint film in this example: 53 parts of polyurethane; 10 parts of carbon nanofiber coated with indium chloride; 4 parts of acrylate; 6 parts of fumed silica; 2.5 parts of fluorine-modified acrylate; T-12 organotin drier 3 parts; 3 parts of compound of aniline oxalic acid light absorber and hindered amine light stabilizer (1:1 by mass ratio); 1 part of dibutyl phthalate; 0.6 part of o-benzoylsulfonimide ; 35 parts of polyether polyols.
步骤1:将53份聚氨酯加入干净的容器中,以600rpm的搅拌速度边搅拌边加10份氯化铟包覆纳米碳纤维、1份邻苯二甲酸二丁酯、4份丙烯酸酯、6份气相二氧化硅,待所有试剂加入后以600rpm的搅拌速度继续搅拌20分钟;Step 1: Add 53 parts of polyurethane to a clean container, and add 10 parts of indium chloride-coated carbon nanofibers, 1 part of dibutyl phthalate, 4 parts of acrylate, and 6 parts of gas phase while stirring at a stirring speed of 600 rpm Silicon dioxide, after all the reagents are added, continue to stir for 20 minutes at a stirring speed of 600rpm;
步骤2:在步骤1的浆料中以550rpm的搅拌速度边搅拌边加入2.5份氟改性丙烯酸酯、3份有机锡催干剂T-12、0.6份邻苯甲酰磺酰亚胺、3份苯胺乙二酸光吸收剂与受阻胺光稳定剂复合物。全部试剂加入后搅拌20min,静置至气泡完全消失;Step 2: Add 2.5 parts of fluorine-modified acrylate, 3 parts of organotin drier T-12, 0.6 parts of o-benzoylsulfonimide, 3 parts of A compound of aniline oxalic acid light absorber and hindered amine light stabilizer. Stir for 20 minutes after adding all the reagents, and let it stand until the bubbles completely disappear;
步骤3:在步骤2制备的浆料中,加入35份聚醚多元醇,混合均匀,然后将浆料调节至合适黏度。Step 3: Add 35 parts of polyether polyol to the slurry prepared in step 2, mix well, and then adjust the slurry to a suitable viscosity.
步骤4:将步骤3中的浆料喷涂于低碳钢板上。Step 4: Spray the slurry in step 3 on the low carbon steel plate.
步骤5:将步骤4的试件在室温下静置、晾干,各项技术指标结果见表2。Step 5: Let the test piece of step 4 stand at room temperature and dry, and the results of various technical indicators are shown in Table 2.
实施例3Example 3
本实施例漆膜组份:聚氨酯55份;氯化铟包覆纳米碳纤维12份;丙烯酸酯4份;气相二氧化硅6份;氟改性丙烯酸酯2.5份;T-12有机锡催干剂3份;苯胺乙二酸光吸收剂与受阻胺光稳定剂复合物(按质量比1:1复合)3份;邻苯二甲酸二丁酯1份;邻苯甲酰磺酰亚胺0.6份;聚醚多元醇35份。Components of the paint film in this example: 55 parts of polyurethane; 12 parts of carbon nanofiber coated with indium chloride; 4 parts of acrylate; 6 parts of fumed silica; 2.5 parts of fluorine-modified acrylate; T-12 organotin drier 3 parts; 3 parts of compound of aniline oxalic acid light absorber and hindered amine light stabilizer (1:1 by mass ratio); 1 part of dibutyl phthalate; 0.6 part of o-benzoylsulfonimide ; 35 parts of polyether polyols.
步骤1:将55份聚氨酯加入干净的容器中,以600rpm的搅拌速度边搅拌边加12份氯化铟包覆纳米碳纤维、1份邻苯二甲酸二丁酯、4份丙烯酸酯、6份气相二氧化硅,待所有试剂加入后以600rpm的搅拌速度继续搅拌20分钟;Step 1: Add 55 parts of polyurethane to a clean container, and add 12 parts of indium chloride-coated carbon nanofibers, 1 part of dibutyl phthalate, 4 parts of acrylate, and 6 parts of gas phase while stirring at a stirring speed of 600 rpm Silicon dioxide, after all the reagents are added, continue to stir for 20 minutes at a stirring speed of 600rpm;
步骤2:在步骤1的浆料中以550rpm的搅拌速度边搅拌边加入2.5份氟改性丙烯酸酯、3份有机锡催干剂T-12、0.6份邻苯甲酰磺酰亚胺、3份苯胺乙二酸光吸收剂与受阻胺光稳定剂复合物。全部试剂加入后以550rpm的搅拌速度搅拌20min,静置至气泡完全消失;Step 2: Add 2.5 parts of fluorine-modified acrylate, 3 parts of organotin drier T-12, 0.6 parts of o-benzoylsulfonimide, 3 parts of A compound of aniline oxalic acid light absorber and hindered amine light stabilizer. After adding all the reagents, stir at a stirring speed of 550rpm for 20min, and let it stand until the bubbles completely disappear;
步骤3:在步骤2制备的浆料中,加入35份聚醚多元醇,混合均匀,然后将浆料调节至合适黏度。Step 3: Add 35 parts of polyether polyol to the slurry prepared in step 2, mix well, and then adjust the slurry to a suitable viscosity.
步骤4:将步骤3中的浆料喷涂于低碳钢板上。Step 4: Spray the slurry in step 3 on the low carbon steel plate.
步骤5:将步骤4的试件在室温下静置、晾干,各项技术指标结果见表3。Step 5: Let the test piece of step 4 stand at room temperature and dry, and the results of various technical indicators are shown in Table 3.
实施例4Example 4
本实施例漆膜组份:聚氨酯55份;氯化铟包覆纳米碳纤维12份;丙烯酸酯4份;气相二氧化硅6份;氟改性丙烯酸酯2.5份;T-12有机锡催干剂3份;苯胺乙二酸光吸收剂与受阻胺光稳定剂复合物(按质量比1:1复合)3份;邻苯二甲酸二丁酯1份;邻苯甲酰磺酰亚胺0.6份;聚醚多元醇35份。Components of the paint film in this example: 55 parts of polyurethane; 12 parts of carbon nanofiber coated with indium chloride; 4 parts of acrylate; 6 parts of fumed silica; 2.5 parts of fluorine-modified acrylate; T-12 organotin drier 3 parts; 3 parts of compound of aniline oxalic acid light absorber and hindered amine light stabilizer (1:1 by mass ratio); 1 part of dibutyl phthalate; 0.6 part of o-benzoylsulfonimide ; 35 parts of polyether polyols.
步骤1:将55份聚氨酯加入干净的容器中,以550rpm的搅拌速度边搅拌边加12份氯化铟包覆纳米碳纤维、1份邻苯二甲酸二丁酯、4份丙烯酸酯、6份气相二氧化硅,待所有试剂加入后继续搅拌30分钟;Step 1: Add 55 parts of polyurethane to a clean container, and add 12 parts of indium chloride-coated carbon nanofibers, 1 part of dibutyl phthalate, 4 parts of acrylate, and 6 parts of gas phase while stirring at a stirring speed of 550 rpm Silica, continue to stir for 30 minutes after all the reagents are added;
步骤2:在步骤1的浆料中以550rpm的搅拌速度边搅拌边加入2.5份氟改性丙烯酸酯、3份有机锡催干剂T-12、0.6份邻苯甲酰磺酰亚胺、3份苯胺乙二酸光吸收剂与受阻胺光稳定剂复合物。全部试剂加入后搅拌25min,静置至气泡完全消失;Step 2: Add 2.5 parts of fluorine-modified acrylate, 3 parts of organotin drier T-12, 0.6 parts of o-benzoylsulfonimide, 3 parts of A compound of aniline oxalic acid light absorber and hindered amine light stabilizer. Stir for 25 minutes after adding all the reagents, and let it stand until the bubbles completely disappear;
步骤3:在步骤2制备的浆料中,加入35份聚醚多元醇,混合均匀,然后将浆料调节至合适黏度。Step 3: Add 35 parts of polyether polyol to the slurry prepared in step 2, mix well, and then adjust the slurry to a suitable viscosity.
步骤4:将步骤3中的浆料喷涂于低碳钢板上。Step 4: Spray the slurry in step 3 on the low carbon steel plate.
步骤5:将步骤4的试件在室温下静置、晾干,各项技术指标结果见表4。Step 5: Let the test piece of step 4 stand at room temperature and dry, and the results of various technical indicators are shown in Table 4.
实施例5Example 5
本实施例漆膜组份:聚氨酯60份;氯化铟包覆纳米碳纤维10份;丙烯酸酯4份;气相二氧化硅6份;氟改性丙烯酸酯2.5份;T-12有机锡催干剂3份;苯胺乙二酸光吸收剂与受阻胺光稳定剂复合物(按质量比1:1复合)3份;邻苯二甲酸二丁酯1份;邻苯甲酰磺酰亚胺0.6份;聚醚多元醇35份。Components of the paint film in this example: 60 parts of polyurethane; 10 parts of carbon nanofiber coated with indium chloride; 4 parts of acrylate; 6 parts of fumed silica; 2.5 parts of fluorine-modified acrylate; T-12 organotin drier 3 parts; 3 parts of compound of aniline oxalic acid light absorber and hindered amine light stabilizer (1:1 by mass ratio); 1 part of dibutyl phthalate; 0.6 part of o-benzoylsulfonimide ; 35 parts of polyether polyols.
步骤1:将60份聚氨酯加入干净的容器中,以600rpm的搅拌速度边搅拌边加10份氯化铟包覆纳米碳纤维、1份邻苯二甲酸二丁酯、4份丙烯酸酯、6份气相二氧化硅,待所有试剂加入后以600rpm的搅拌速度继续搅拌20分钟;Step 1: Add 60 parts of polyurethane to a clean container, and add 10 parts of indium chloride-coated carbon nanofibers, 1 part of dibutyl phthalate, 4 parts of acrylate, and 6 parts of gas phase while stirring at a stirring speed of 600 rpm Silicon dioxide, after all the reagents are added, continue to stir for 20 minutes at a stirring speed of 600rpm;
步骤2:在步骤1的浆料中以550rpm的搅拌速度边搅拌边加入2.5份氟改性丙烯酸酯、3份有机锡催干剂T-12、0.6份邻苯甲酰磺酰亚胺、3份苯胺乙二酸光吸收剂与受阻胺光稳定剂复合物。全部试剂加入后以550rpm的搅拌速度搅拌20min,静置至气泡完全消失;Step 2: Add 2.5 parts of fluorine-modified acrylate, 3 parts of organotin drier T-12, 0.6 parts of o-benzoylsulfonimide, 3 parts of A compound of aniline oxalic acid light absorber and hindered amine light stabilizer. After adding all the reagents, stir at a stirring speed of 550rpm for 20min, and let it stand until the bubbles completely disappear;
步骤3:在步骤2制备的浆料中,加入35份聚醚多元醇,混合均匀,然后将浆料调节至合适黏度。Step 3: Add 35 parts of polyether polyol to the slurry prepared in step 2, mix well, and then adjust the slurry to a suitable viscosity.
步骤4:将步骤3中的浆料喷涂于低碳钢板上。Step 4: Spray the slurry in step 3 on the low carbon steel plate.
步骤5:将步骤4的试件在室温下静置、晾干,各项技术指标结果见表5。Step 5: Let the test piece of step 4 stand at room temperature and dry, and the results of various technical indicators are shown in Table 5.
表1Table 1
表2Table 2
表3table 3
表4Table 4
表5table 5
以上结果表明,按照本发明的成分配比制备出的防腐耐冲击面漆具有高韧性、高耐冲击性、高结合强度等性能,能够满足飞溅区等恶劣环境对漆膜面层高寿命、长检修周期的需求。The above results show that the anti-corrosion and impact-resistant top paint prepared according to the composition ratio of the present invention has properties such as high toughness, high impact resistance, and high bonding strength, and can meet the requirements of harsh environments such as splash zones for high life and long life of the paint film surface. maintenance cycle requirements.
需要说明的是,以上所述仅为本发明实施方式的一部分,根据本发明所描述的系统所做的等效变化,均包括在本发明的保护范围内。本发明所属技术领域的技术人员可以对所描述的具体实例做类似的方式替代,只要不偏离本发明的结构或者超越本权利要求书所定义的范围,均属于本发明的保护范围。It should be noted that the above description is only a part of the embodiments of the present invention, and equivalent changes made according to the system described in the present invention are all included in the protection scope of the present invention. Those skilled in the art to which the present invention belongs can replace the described specific examples in a similar manner, as long as they do not deviate from the structure of the present invention or exceed the scope defined in the claims, they all belong to the protection scope of the present invention.
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