CN110760238A - A kind of powder coating and preparation method thereof - Google Patents
A kind of powder coating and preparation method thereof Download PDFInfo
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- CN110760238A CN110760238A CN201911043643.3A CN201911043643A CN110760238A CN 110760238 A CN110760238 A CN 110760238A CN 201911043643 A CN201911043643 A CN 201911043643A CN 110760238 A CN110760238 A CN 110760238A
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- 238000000576 coating method Methods 0.000 title claims abstract description 80
- 239000011248 coating agent Substances 0.000 title claims abstract description 64
- 239000000843 powder Substances 0.000 title claims abstract description 56
- 238000002360 preparation method Methods 0.000 title claims description 12
- 239000003822 epoxy resin Substances 0.000 claims abstract description 16
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 16
- 239000000945 filler Substances 0.000 claims abstract description 8
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 7
- 239000010445 mica Substances 0.000 claims description 9
- 229910052618 mica group Inorganic materials 0.000 claims description 9
- 238000001125 extrusion Methods 0.000 claims description 7
- 239000004593 Epoxy Substances 0.000 claims description 6
- 238000005507 spraying Methods 0.000 claims description 6
- 239000004841 bisphenol A epoxy resin Substances 0.000 claims description 5
- -1 cyanamide compound Chemical class 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 5
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 4
- 238000005303 weighing Methods 0.000 claims description 2
- 238000010298 pulverizing process Methods 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract description 15
- 238000009413 insulation Methods 0.000 abstract description 14
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract description 10
- 239000000463 material Substances 0.000 abstract description 8
- 239000003960 organic solvent Substances 0.000 abstract description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract description 5
- 239000002253 acid Substances 0.000 abstract description 5
- 239000003513 alkali Substances 0.000 abstract description 5
- 239000008096 xylene Substances 0.000 abstract description 5
- 239000000049 pigment Substances 0.000 abstract description 4
- 239000012752 auxiliary agent Substances 0.000 abstract description 2
- 239000007921 spray Substances 0.000 abstract description 2
- 230000000052 comparative effect Effects 0.000 description 11
- 239000002994 raw material Substances 0.000 description 6
- 229910000859 α-Fe Inorganic materials 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical group C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000011056 performance test Methods 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical group NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical group CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 244000028419 Styrax benzoin Species 0.000 description 2
- 235000000126 Styrax benzoin Nutrition 0.000 description 2
- 235000008411 Sumatra benzointree Nutrition 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 229960002130 benzoin Drugs 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 235000019382 gum benzoic Nutrition 0.000 description 2
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 238000007590 electrostatic spraying Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000013799 ultramarine blue Nutrition 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
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/4007—Curing agents not provided for by the groups C08G59/42 - C08G59/66
- C08G59/4014—Nitrogen containing compounds
- C08G59/4021—Ureas; Thioureas; Guanidines; Dicyandiamides
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/03—Powdery paints
- C09D5/033—Powdery paints characterised by the additives
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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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/08—Anti-corrosive paints
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
- C08K2003/3045—Sulfates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
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- Chemical & Material Sciences (AREA)
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- Wood Science & Technology (AREA)
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- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
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Abstract
本发明属于材料领域,公开了一种粉末涂料,按重量份计,包含以下组分:环氧树脂150‑200份、改性环氧树脂10‑50份、固化剂5‑20份、固化促进剂0.1‑3份、填料50‑150份、助剂5‑20份、颜料0.5‑10份,所述粉末涂料绝缘性好,耐高压、耐酸碱、耐有机溶剂,喷涂所述粉末涂料200‑300μm时,涂层在5000伏电压下不被击穿;在155℃下持续烘烤400小时后,涂层在5000伏电压下不被击穿;绝缘等级为F;涂层在丙酮中浸泡2h,丁酮中浸泡4h,二甲苯中浸泡24h,涂层均无软化脱落现象;涂层在10%质量浓度的盐酸溶液或10%质量浓度的NaOH溶液中浸泡10天,涂层也不出现起泡脱落现象。The invention belongs to the field of materials, and discloses a powder coating, which comprises the following components in parts by weight: 150-200 parts of epoxy resin, 10-50 parts of modified epoxy resin, 5-20 parts of curing agent, curing accelerator 0.1-3 parts of agent, 50-150 parts of filler, 5-20 parts of auxiliary agent, 0.5-10 parts of pigment, the powder coating has good insulation, high pressure resistance, acid and alkali resistance, organic solvent resistance, spray the powder coating 200 ‑300μm, the coating will not break down under 5000V; after continuous baking at 155℃ for 400 hours, the coating will not break down under 5000V; the insulation class is F; the coating is immersed in acetone 2h, soaked in butanone for 4h, and soaked in xylene for 24h, the coating did not soften and fall off; the coating was soaked in 10% mass concentration hydrochloric acid solution or 10% mass concentration NaOH solution for 10 days, and the coating did not appear. Blistering phenomenon.
Description
技术领域technical field
本发明属于材料领域,特别涉及一种粉末涂料及其制备方法。The invention belongs to the field of materials, in particular to a powder coating and a preparation method thereof.
背景技术Background technique
粉末涂料是以树脂、颜料、填料、助剂等组成的固体粉末状树脂涂料,和普通溶剂型涂料、水性涂料相比,其分散介质不是溶剂和水,而是空气。因此其具有无溶剂污染,100%成膜,涂装效率高,涂层性能优异,能耗低的特点。Powder coatings are solid powder resin coatings composed of resins, pigments, fillers, additives, etc. Compared with ordinary solvent-based coatings and water-based coatings, the dispersion medium is not solvent and water, but air. Therefore, it has the characteristics of no solvent pollution, 100% film formation, high coating efficiency, excellent coating performance and low energy consumption.
随着粉末涂料的广泛使用,粉末涂料在电子、电机用绝缘材料中也占据了越来越重要的地位,粉末涂料广泛应用于电机、电子、汽车工业、航空机械等各个领域。但因高压电器、高压线圈、电感磁圈等高压用机器或材料,工作时处于高电压环境,其电压达到5000伏以上,同时可能接触到有机溶剂和酸碱溶液等,因此对其所用涂料的绝缘性、耐高压性、耐酸碱性、耐有机溶剂性提出了更高的要求,但目前粉末涂料还无法同时满足上述要求,极大地制约了绝缘粉末涂料在该领域的推广与应用。With the widespread use of powder coatings, powder coatings are also playing an increasingly important role in insulating materials for electronics and motors. Powder coatings are widely used in motors, electronics, automotive industry, aviation machinery and other fields. However, because high-voltage electrical appliances, high-voltage coils, inductor coils and other high-voltage machines or materials are in a high-voltage environment when working, the voltage reaches more than 5,000 volts, and at the same time, they may come into contact with organic solvents and acid-base solutions. Insulation, high pressure resistance, acid and alkali resistance, and organic solvent resistance have put forward higher requirements, but the current powder coatings cannot meet the above requirements at the same time, which greatly restricts the promotion and application of insulating powder coatings in this field.
因此,提供一种耐高压、耐酸碱、耐有机溶剂的粉末涂料很有必要。Therefore, it is necessary to provide a powder coating that is resistant to high pressure, acid and alkali, and organic solvents.
发明内容SUMMARY OF THE INVENTION
本发明旨在至少解决现有技术中存在的技术问题之一。为此,本发明提出一种粉末涂料,能够耐高压、耐酸碱、耐有机溶剂。The present invention aims to solve at least one of the technical problems existing in the prior art. To this end, the present invention proposes a powder coating that can withstand high pressure, acid and alkali, and organic solvents.
一种粉末涂料,按重量份计,包含以下组分:A powder coating, by weight, comprises the following components:
优选的,所述粉末涂料,按重量份计,包含以下组分:Preferably, the powder coating, in parts by weight, comprises the following components:
所述环氧树脂为双酚A型环氧树脂。The epoxy resin is a bisphenol A type epoxy resin.
优选的,所述双酚A型环氧树脂的环氧当量为400-1000g/eq;进一步优选的,所述双酚A型环氧树脂的环氧当量为600-900g/eq;更优选的,所述双酚A型环氧树脂的环氧当量为600-700g/eq。Preferably, the epoxy equivalent of the bisphenol A epoxy resin is 400-1000 g/eq; further preferably, the epoxy equivalent of the bisphenol A epoxy resin is 600-900 g/eq; more preferably , the epoxy equivalent of the bisphenol A epoxy resin is 600-700 g/eq.
所述改性环氧树脂为硅烷改性环氧树脂。The modified epoxy resin is a silane-modified epoxy resin.
优选的,所述硅烷改性环氧树脂的环氧当量为100-500g/eq;进一步优选的,所述硅烷改性环氧树脂的环氧当量为200-350g/eq。Preferably, the epoxy equivalent of the silane-modified epoxy resin is 100-500 g/eq; further preferably, the epoxy equivalent of the silane-modified epoxy resin is 200-350 g/eq.
所述填料包含云母粉,优选的,所述云母粉占所述填料的质量的50%-100%。The filler comprises mica powder, preferably, the mica powder accounts for 50%-100% of the mass of the filler.
所述填料还可以包含硫酸钡和/或硅微粉。The filler may also contain barium sulfate and/or silicon micropowder.
所述固化剂为氰胺类化合物,优选的,所述固化剂为双氰胺,所述双氰胺的熔点为209.5℃。The curing agent is a cyanamide compound, preferably, the curing agent is dicyandiamide, and the melting point of the dicyandiamide is 209.5°C.
所述固化促进剂为咪唑类或咪唑类衍生物,优选的,所述固化促进剂为2-甲基咪唑。The curing accelerator is imidazole or imidazole derivatives, preferably, the curing accelerator is 2-methylimidazole.
所述助剂为流平剂、抗氧剂、消泡剂或附着力增加剂中的至少一种。The auxiliary agent is at least one of a leveling agent, an antioxidant, a defoaming agent or an adhesion enhancer.
所述消泡剂为苯偶姻(安息香)。The defoamer is benzoin (benzoin).
所述颜料为粉末涂料通用性颜料,如有机红,炭黑、铁黄、群青。The pigments are general-purpose pigments for powder coatings, such as organic red, carbon black, iron yellow, and ultramarine blue.
所述粉末涂料的粒径为10-50μm;优选的,所述粉末涂料的粒径在25-40μm。The particle size of the powder coating is 10-50 μm; preferably, the particle size of the powder coating is 25-40 μm.
一种粉末涂料的制备方法,包括以下步骤:按比例称取各组分,混合,破碎,再熔融挤出,压片,粉碎,即得所述粉末涂料。A preparation method of powder coating comprises the following steps: weighing each component in proportion, mixing, crushing, melting and extruding, tableting and crushing to obtain the powder coating.
具体来说,一种粉末涂料的制备方法,包括以下步骤:Specifically, a preparation method of powder coating, comprising the following steps:
按比例称取各组分,然后将物料置于搅拌机中充分混合破碎,混合破碎时间为5-15min;将混合好的物料在挤出机上熔融挤出,并压片,然后将片料进行冷却、粉碎、筛分,出粉口处过磁,去除金属杂质,即得粉末涂料。Weigh the components in proportion, and then place the materials in the mixer to fully mix and crush, and the mixing and crushing time is 5-15 minutes; the mixed materials are melted and extruded on the extruder, and pressed into tablets, and then the tablets are cooled. , crushing, sieving, passing the magnet at the powder outlet to remove metal impurities, and then the powder coating is obtained.
所述熔融挤出的温度为一区90-105℃,二区为105-120℃,优选的,步骤(2)中所述熔融挤出的温度为一区100℃,二区为110℃。The temperature of the melt extrusion is 90-105°C in the first zone and 105-120°C in the second zone. Preferably, the melt extrusion temperature in step (2) is 100°C in the first zone and 110°C in the second zone.
一种涂层,将所述粉末涂料进行喷涂,在200℃下,固化5-10min而制得。所述涂层的厚度为100-300μm。A coating is prepared by spraying the powder coating and curing at 200° C. for 5-10 minutes. The thickness of the coating is 100-300 μm.
一种电器设备,包括所述涂层。An electrical device includes the coating.
将所述粉末涂料应用于高压用机器或材料。The powder coating is applied to high pressure machines or materials.
相对于现有技术,本发明的有益效果如下:With respect to the prior art, the beneficial effects of the present invention are as follows:
用环氧树脂与硅烷改性环氧树脂作为树脂主体,氰胺类化合物为固化剂,反应交联密度大。硅烷改性环氧树脂中的硅氧烷结构在反应固化后,硅氧烷部分向表面迁移,使得涂层表面具有有机硅类似的性能,增加涂层的疏水性和热稳定性。同时粉末涂料中加入大量云母粉作为填料,云母粉中二氧化硅与三氧化二铝复合形成复式硅氧层,宏观表现为片状结构;在涂装过程中,云母晶片在漆膜固化前受到表面张力的作用而躺下,自动形成互相平行,且与漆膜表面也平行的结构,这样的层层排列,其取向正好与腐蚀性物质穿透漆膜的方向相垂直,阻隔作用强;而且云母本身具有极高的电阻,是优异绝缘材料,与树脂混后,加强了涂层的绝缘性和耐高压性。The epoxy resin and silane modified epoxy resin are used as the main resin, and the cyanamide compound is used as the curing agent, and the reaction crosslinking density is high. After the siloxane structure in the silane-modified epoxy resin is cured by reaction, the siloxane part migrates to the surface, so that the surface of the coating has properties similar to silicone, which increases the hydrophobicity and thermal stability of the coating. At the same time, a large amount of mica powder is added to the powder coating as a filler, and the silica in the mica powder is compounded with aluminum oxide to form a composite silica layer, which has a macroscopic appearance of a sheet-like structure; during the coating process, the mica wafer is subjected to Under the action of surface tension, it will automatically form a structure that is parallel to each other and parallel to the surface of the paint film. Such layer-by-layer arrangement, its orientation is just perpendicular to the direction in which corrosive substances penetrate the paint film, and the barrier effect is strong; Mica itself has extremely high resistance and is an excellent insulating material. After mixing with resin, it strengthens the insulation and high pressure resistance of the coating.
因此使得所述粉末涂料绝缘性好,耐高压、耐酸碱、耐有机溶剂,喷涂所述粉末涂料200-300μm时,涂层在5000伏电压下不被击穿;在155℃下持续烘烤400小时后,涂层在5000伏电压下也不被击穿;绝缘等级为F;涂层在丙酮中浸泡2小时,丁酮中浸泡4小时,二甲苯中浸泡24小时,涂层均无无软化脱落现象;涂层在10%质量浓度盐酸溶液或10%质量浓度NaOH溶液中浸泡10天,涂层也无起泡脱落现象。Therefore, the powder coating has good insulation, high voltage resistance, acid and alkali resistance, and organic solvent resistance. When the powder coating is sprayed at 200-300 μm, the coating will not be broken down at 5000 volts; continuous baking at 155 ° C After 400 hours, the coating is not broken down under 5000 volts; the insulation class is F; the coating is soaked in acetone for 2 hours, butanone for 4 hours, and xylene for 24 hours. Softening and peeling phenomenon; the coating is soaked in 10% mass concentration hydrochloric acid solution or 10% mass concentration NaOH solution for 10 days, and the coating has no blistering and peeling phenomenon.
本发明所述粉末涂料,配方简单、节能环保,能部分取代油漆涂料产品,有机挥发物(VOC)为零。The powder coating of the invention has the advantages of simple formula, energy saving and environmental protection, can partially replace paint and coating products, and has zero organic volatile compounds (VOC).
具体实施方式Detailed ways
为了让本领域技术人员更加清楚明白本发明所述技术方案,现列举以下实施例进行说明。需要指出的是,以下实施例对本发明要求的保护范围不构成限制作用。In order to make those skilled in the art understand the technical solutions of the present invention more clearly, the following examples are now given for illustration. It should be noted that the following examples do not limit the protection scope of the present invention.
实施例1-6,按表1粉末涂料的组成,称取各组分,然后将物料置于搅拌机中充分混合破碎,混合破碎时间为5-15min,再将混合好的物料在挤出机上熔融挤出,熔融挤出的温度为一区90-105℃,二区为105-120℃,熔融挤出后压片,然后将片料进行冷却、粉碎、筛分,出粉口处过磁,去除金属杂质,即得粉末涂料。Examples 1-6, according to the composition of the powder coating in Table 1, weigh each component, then place the material in a mixer to fully mix and crush, and the mixing and crushing time is 5-15min, and then the mixed material is melted on the extruder Extrusion, the temperature of melt extrusion is 90-105°C in the first zone and 105-120°C in the second zone. After melt extrusion, the tablet is pressed, and then the tablet is cooled, pulverized and sieved, and the powder outlet is magnetically passed. Remove metal impurities to obtain powder coating.
表1粉末涂料的组成Table 1 Composition of powder coatings
对比例1Comparative Example 1
将实施例1中50份云母粉换为30份,其余原料与制备方法同实施例1。The 50 parts of mica powder in Example 1 were replaced with 30 parts, and the remaining raw materials and preparation methods were the same as those of Example 1.
对比例2Comparative Example 2
将实施例1中180份双酚A型环氧树脂改为120份,其余原料与制备方法同实施例1。The 180 parts of bisphenol A epoxy resin in Example 1 were changed to 120 parts, and the remaining raw materials and preparation methods were the same as those of Example 1.
对比例3Comparative Example 3
将实施例1中20份硅烷改性环氧树脂改为5份,其余原料与制备方法同实施例1。The 20 parts of silane-modified epoxy resin in Example 1 were changed to 5 parts, and the remaining raw materials and preparation methods were the same as those of Example 1.
对比例4Comparative Example 4
将实施例1中1.5份2-甲基咪唑改为5份,其余原料与制备方法同实施例1。Change 1.5 parts of 2-methylimidazole in Example 1 to 5 parts, and the remaining raw materials and preparation methods are the same as those of Example 1.
对比例5Comparative Example 5
将实施例1中11.5份微粉化双氰胺改为4.5份,其余原料与制备方法同实施例1。In Example 1, 11.5 parts of micronized dicyandiamide were changed to 4.5 parts, and the rest of the raw materials and the preparation method were the same as those of Example 1.
对比例6Comparative Example 6
将实施例1制备过程中熔融挤出的温度,一区温度90-105℃改为80℃,二区温度105-120℃改为125℃,其余原料与制备方法同实施例1。The temperature of melt extrusion in the preparation process of Example 1 was changed to 80°C from 90-105°C in the first zone, and 125°C from 105-120°C in the second zone. The remaining raw materials and preparation methods were the same as those in Example 1.
产品效果测试Product effect test
将上述实施例1-6,对比例1-6所得粉末涂料,分别通过高压静电喷涂方式,喷涂于预先在200℃烘箱中预热的铁氧体磁圈上,涂层厚度在200-300μm之间,固化条件为:200℃,5-10min。The powder coatings obtained in the above Examples 1-6 and Comparative Examples 1-6 were respectively sprayed on the ferrite coils preheated in a 200 ℃ oven by high-voltage electrostatic spraying, and the coating thickness was between 200-300 μm. The curing conditions are: 200℃, 5-10min.
将喷涂实施例1-6,对比例1-6所得粉末涂料的铁氧体磁圈分别进行性能测试:The ferrite coils of the powder coatings obtained by spraying Examples 1-6 and Comparative Examples 1-6 are respectively tested for performance:
其中,附着力根据GB/T 9286进行测试;抗冲击性根据GB/T 1732进行测试;中性盐雾根据GB/T 1771-2007进行测试;表观密度根据GB/T 6554-2003进行测试;击穿强度(常温)根据GB/T 6554-2003进行测试;绝缘等级根据GB/T 11021-2007进行测试。Among them, the adhesion is tested according to GB/T 9286; the impact resistance is tested according to GB/T 1732; the neutral salt spray is tested according to GB/T 1771-2007; the apparent density is tested according to GB/T 6554-2003; The breakdown strength (room temperature) is tested according to GB/T 6554-2003; the insulation grade is tested according to GB/T 11021-2007.
同时对铁氧体磁圈进行以下测试:At the same time, perform the following tests on the ferrite coil:
(1)于5000伏电压下进行测试;(1) Test at 5000 volts;
(2)在155℃下持续烘烤400小时后,于5000伏电压下进行测试;(2) After continuous baking at 155°C for 400 hours, test at 5000 volts;
(3)分别浸泡在丙酮中2小时、丁酮中4小时、二甲苯中24小时;(3) soak in acetone for 2 hours, butanone for 4 hours, and xylene for 24 hours;
(4)浸泡在10%质量浓度NaOH溶液10天;(4) soak in 10% mass concentration NaOH solution for 10 days;
(5)浸泡在10%质量浓度盐酸溶液中10天。(5) Soak in 10% mass concentration hydrochloric acid solution for 10 days.
实施例1-6性能测试结果见表2,对比例1-6性能测试结果见表3。The performance test results of Examples 1-6 are shown in Table 2, and the performance test results of Comparative Examples 1-6 are shown in Table 3.
表2实施例1-6性能测试结果Table 2 embodiment 1-6 performance test results
其中,绝缘等级分为A、E、B、F、H、5个级别:A级绝缘耐温105℃;E级绝缘耐温120℃;B级绝缘耐温130℃;F级绝缘耐温155℃;H级绝缘耐温180℃。Among them, the insulation grades are divided into A, E, B, F, H, 5 grades: A grade insulation temperature resistance 105 ℃; E grade insulation temperature resistance 120 ℃; B grade insulation temperature resistance 130 ℃; F grade insulation temperature resistance 155 ℃; H-class insulation temperature resistance 180 ℃.
表3对比例1-6性能测试结果Table 3 Comparative Examples 1-6 Performance Test Results
由表2、表3对比可知,喷涂实施例1-6所得粉末涂料的铁氧体磁圈性能明显优于对比例1-6,喷涂实施例1-6所得粉末涂料的铁氧体磁圈绝缘等级均为F,于5000伏电压下涂层不击穿;在155℃下持续烘烤400小时后,于5000伏电压下涂层仍不击穿;浸泡在丙酮中2小时、丁酮中4小时、二甲苯中24小时均不会出现涂层起泡软化现象;浸泡在10%质量浓度NaOH溶液10天或浸泡在10%质量浓度盐酸溶液中10天涂层也不出现起泡软化。而喷涂实施例1-6所得粉末涂料的铁氧体磁圈无论是在5000伏电压下测试,还是于155℃下持续烘烤400小时后测试,涂层均被击穿;浸泡在丙酮中2小时、丁酮中4小时、二甲苯中24小时,或浸泡在10%质量浓度NaOH溶液/盐酸溶液10天,涂层会会出现起泡软化现象。It can be seen from the comparison of Table 2 and Table 3 that the performance of the ferrite coil of the powder coating obtained by spraying Example 1-6 is obviously better than that of Comparative Example 1-6, and the ferrite coil insulation of the powder coating obtained by spraying Example 1-6 All grades are F, the coating does not break down at 5000 volts; after continuous baking at 155 ° C for 400 hours, the coating still does not break down at 5000 volts; immersed in acetone for 2 hours, butanone for 4 hours No foaming and softening of the coating occurred in 24 hours and xylene for 24 hours; no foaming and softening occurred in the coating after immersion in 10% mass concentration NaOH solution for 10 days or in 10% mass concentration hydrochloric acid solution for 10 days. However, whether the ferrite coils of the powder coatings obtained by spraying Examples 1-6 were tested at a voltage of 5000 volts or after being continuously baked at 155°C for 400 hours, the coatings were all broken down; soaked in acetone for 2 hours, 4 hours in butanone, 24 hours in xylene, or immersed in 10% mass concentration NaOH solution/hydrochloric acid solution for 10 days, the coating will foam and soften.
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