[go: up one dir, main page]

CN103031014B - A kind of preparation method of non-conductive substrate powder paint coating - Google Patents

A kind of preparation method of non-conductive substrate powder paint coating Download PDF

Info

Publication number
CN103031014B
CN103031014B CN201210537047.2A CN201210537047A CN103031014B CN 103031014 B CN103031014 B CN 103031014B CN 201210537047 A CN201210537047 A CN 201210537047A CN 103031014 B CN103031014 B CN 103031014B
Authority
CN
China
Prior art keywords
low
viscosity
coating
epoxy resin
resin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201210537047.2A
Other languages
Chinese (zh)
Other versions
CN103031014A (en
Inventor
薛杨
张冬海
刘海弟
吴镇江
陈运法
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Institute of Process Engineering of CAS
Original Assignee
Institute of Process Engineering of CAS
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Institute of Process Engineering of CAS filed Critical Institute of Process Engineering of CAS
Priority to CN201210537047.2A priority Critical patent/CN103031014B/en
Publication of CN103031014A publication Critical patent/CN103031014A/en
Application granted granted Critical
Publication of CN103031014B publication Critical patent/CN103031014B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Application Of Or Painting With Fluid Materials (AREA)
  • Paints Or Removers (AREA)

Abstract

The present invention relates to a kind of preparation method of non-conductive substrate powder paint coating, described method comprises the steps: that (1) is to non-conductive substrate coating low-viscosity (mobile) liquid resin combination; (2) to the non-conductive substrate spray coating powder paint being coated with low-viscosity (mobile) liquid resin combination, be heating and curing, form powder coating.Gained paint coating thickness of the present invention is 5 ~ 200 μm and controlled, and coating surface is smooth, coating flatness≤3 μm.Compared to conventional electrostatic spraying, can be used for non-conductive substrate, and there is the advantages such as adhesive force is good, the saving energy, technique are simple.Described method is applicable to the non-conducting materials such as timber, paper, cement, glass, plastics, pottery, is particularly useful for timber.

Description

一种非导电基材粉末涂料涂层的制备方法A kind of preparation method of non-conductive substrate powder paint coating

技术领域technical field

本发明涉及一种非导电基材粉末涂料涂层的制备方法,属于涂料涂层领域。The invention relates to a preparation method of a non-conductive substrate powder paint coating, which belongs to the field of paint coatings.

背景技术Background technique

近年来,粉末涂料以其省资源、省能源、无污染、效率高、易实现自动化等特点,成为发展最快的涂料品种。粉末涂料主要用在金属物件上涂敷装饰涂层。该涂料是在静电场中,通过将干的着色颗粒从摩擦或者静电激化的专用涂布器内喷向物件,颗粒通过静电力而粘附到物件上。粉末涂敷的优点是可对多种结构和表面进行修饰,涂层非常牢固,抗磨损,外用品级耐风蚀。另外,粉末涂敷法不用溶剂,由于粉末能回收并重复利用,所以几乎没有浪费。在物件上的涂层厚度可以精确地控制。再有,本方法特别适用于形状复杂的物件的涂敷。最后,粉末涂敷具有柔韧性和粘附特性,因此,在粉末涂敷之后,平板之类的物件涂层后可形成卷曲和卷边。In recent years, powder coating has become the fastest-growing coating variety due to its resource-saving, energy-saving, pollution-free, high efficiency, and easy automation. Powder coatings are mainly used to apply decorative coatings on metal objects. The paint is applied in an electrostatic field by spraying dry colored particles from a friction or electrostatically excited special applicator onto the object, and the particles adhere to the object by electrostatic force. The advantage of powder coating is that it can modify a variety of structures and surfaces, the coating is very strong, wear-resistant, and the external grade is wind-resistant. In addition, the powder coating method does not use solvents, and since the powder can be recovered and reused, there is almost no waste. The thickness of the coating on the object can be precisely controlled. Furthermore, the method is particularly suitable for coating objects with complex shapes. Finally, powder coating has flexibility and adhesive properties, so objects such as flat panels can be coated to form curls and curls after powder coating.

目前粉末涂料在一些热敏性材料如木材、纸张、塑料、玻璃等领域也开始得到应用,为此人们积极展开了对粉末涂料工艺的研究和开发,并取得了一定成果,但由于粉末涂料最常用的是静电喷涂法,这就需要基体材料具有一定的导电性。对于非导电或导电性差的基材,通常是先涂一层导电涂料提高导电性,然后再进行涂装。At present, powder coatings have also begun to be applied in some heat-sensitive materials such as wood, paper, plastic, glass and other fields. For this reason, people have actively carried out research and development on powder coating technology and achieved certain results. However, due to the most commonly used powder coating It is an electrostatic spraying method, which requires the base material to have a certain conductivity. For non-conductive or poorly conductive substrates, a layer of conductive paint is usually applied to improve conductivity before painting.

CN101342526公开了一种在木材部件表面固化粉末涂料的方法,但仅将木材加热至60~80℃很难将粉末涂料附着于表面,难于成型;WO01/30927公开的将粉末涂料涂覆在非金属基材上的方法,但该方法预涂聚合物需要使用可溶性潜伏催化剂;CN101186780公开了一种紫外光固化粉末涂料及其生产方法、涂装方法来解决不耐高温和厚质底材的涂装问题,但该方法受到光固化树脂制备技术和设备造价的限制;CN1226301公开了一种在木质纤维素材料段上涂敷粉末涂料的方法,但该方法浸渍后要去除溶剂,低温固化需使用紫外光固化,工艺相对复杂。CN101342526 discloses a method for solidifying powder coatings on the surface of wood parts, but it is difficult to attach the powder coatings to the surface only by heating the wood to 60-80 ° C, and it is difficult to shape; WO01/30927 discloses coating powder coatings on non-metallic The method on the base material, but this method needs to use soluble latent catalyst for pre-coating polymer; CN101186780 discloses a kind of ultraviolet curing powder coating and its production method, coating method to solve the coating of not resistant to high temperature and thick substrate problem, but the method is limited by photocurable resin preparation technology and equipment cost; CN1226301 discloses a method for coating powder coatings on lignocellulosic material segments, but the method will remove solvent after impregnation, and low temperature curing needs to use ultraviolet light Light curing, the process is relatively complicated.

发明内容Contents of the invention

本发明的目的在于提供一种非导电基材粉末涂料涂层的制备方法,所述方法工艺简单,涂层均匀,涂层后的非导电基材表面涂层均匀、硬度高、附着力优异。The object of the present invention is to provide a method for preparing a non-conductive base material powder paint coating. The method has simple process and uniform coating, and the surface coating of the non-conductive base material after coating is uniform, has high hardness and excellent adhesion.

为了达到上述目的,本发明采用了如下技术方案:In order to achieve the above object, the present invention adopts following technical scheme:

一种非导电基材粉末涂料涂层的制备方法,所述方法包括如下步骤:A kind of preparation method of non-conductive substrate powder coating, described method comprises the steps:

(1)对非导电基材涂敷低粘度液体树脂组合物;(1) Applying a low-viscosity liquid resin composition to a non-conductive substrate;

(2)对涂敷有低粘度液体树脂组合物的非导电基材喷涂粉末涂料,加热固化,形成粉末涂层。(2) Spraying a powder coating on the non-conductive substrate coated with the low-viscosity liquid resin composition, heating and curing to form a powder coating.

本发明首先采用低粘度液体树脂对非导电基材涂覆处理,利用树脂的良好流动性渗入到非导电基材表层中,起到提高表面硬度和附着力的效果;另外,利用树脂的粘附性粘附粉末涂料,有利于控制涂层的均匀性,提高涂层的相容性。由于低粘度液体树脂的良好混溶性,在较高温度下,其可与液态的粉末涂料相混并一起均匀固化,从而实现对非导电基材的粉末涂料涂装。由于低粘度液体树脂良好的渗透作用,相对于预涂导电涂层工艺,本发明工艺所得产品具有更强的附着力。The present invention first adopts the low-viscosity liquid resin to coat the non-conductive substrate, and utilizes the good fluidity of the resin to infiltrate into the surface layer of the non-conductive substrate to improve the surface hardness and adhesion; in addition, the adhesion of the resin is utilized Non-adhesive powder coating, which is beneficial to control the uniformity of the coating and improve the compatibility of the coating. Due to the good miscibility of the low-viscosity liquid resin, it can be mixed with the liquid powder coating and solidified uniformly at a higher temperature, so as to realize the powder coating coating on the non-conductive substrate. Due to the good penetration of the low-viscosity liquid resin, compared with the pre-coating conductive coating process, the product obtained by the process of the present invention has stronger adhesion.

优选地,步骤(1)前对非导电基材表面进行预处理。所述预处理包括清理非导电基材表面灰尘和污物,把粗糙表面磨平打光。Preferably, the surface of the non-conductive substrate is pretreated before step (1). The pretreatment includes cleaning dust and dirt on the surface of the non-conductive substrate, and smoothing the rough surface.

本发明所述非导电基材选自木材、纸张、水泥、玻璃、塑料或陶瓷中的任意一种或者至少两种的混合物,优选木材。The non-conductive substrate of the present invention is selected from any one or a mixture of at least two of wood, paper, cement, glass, plastic or ceramics, preferably wood.

所述低粘度液体树脂组合物选自低粘度液体树脂、低粘度液体树脂和溶剂的混合物、低粘度液体树脂和固化剂的混合物中的任意一种或者至少两种的组合。所述低粘度液体树脂和溶剂的混合物、低粘度液体树脂和固化剂的混合物即利用溶剂或固化剂对低粘度液体树脂进行稀释后形成的混合物。所述低粘度液体树脂组合物既可以是低粘度液体树脂也可以是固化剂或溶剂稀释后所形成的混合物,或者是至少两种的组合,均可实现本发明。The low-viscosity liquid resin composition is selected from any one or a combination of at least two of low-viscosity liquid resins, mixtures of low-viscosity liquid resins and solvents, mixtures of low-viscosity liquid resins and curing agents. The mixture of the low-viscosity liquid resin and solvent, and the mixture of low-viscosity liquid resin and curing agent are the mixture formed by diluting the low-viscosity liquid resin with solvent or curing agent. The low-viscosity liquid resin composition can be either a low-viscosity liquid resin or a mixture formed after dilution by a curing agent or a solvent, or a combination of at least two of them, all of which can realize the present invention.

上述固化剂可采用该种树脂在该领域内常用的或者通用的固化剂,如巴斯夫的BaxxodurTMEC301、BaxxodurTMEC110、BaxxodurTMEC331、HI190BS、HI-190;德国科宁的Versamid100、Versamid115、Genamid151;德国拜耳的DesmodurN3390、DesmodurN75;阿克苏诺贝尔的TrigonoxV388、ButanoxM-50,优选巴斯夫的BaxxodurTMEC301、阿克苏诺贝尔的TrigonoxV388。The above-mentioned curing agent can adopt the commonly used or general curing agent of this kind of resin in this field, such as Baxxodur TM EC301, Baxxodur TM EC110, Baxxodur TM EC331, HI190BS, HI-190 of BASF; Versamid100, Versamid115, Genamid151 of German Koning ; DesmodurN3390, DesmodurN75 of Bayer, Germany; TrigonoxV388, ButanoxM-50 of AkzoNobel, preferably Baxxodur TM EC301 of BASF, TrigonoxV388 of AkzoNobel.

所述溶剂,作为具体例,可以举出甲醇、乙醇、丁醇等醇类,乙基溶纤剂、丁基溶纤剂、乙二醇-甲醚、卡必醇、丁基卡必醇等醚类,丙酮、丁酮、甲基乙基甲酮、甲基异丁基甲酮、环己酮等酮类,甲苯、二甲苯、均三甲苯等芳香族烃类,乙氧基乙基乙酸酯、醋酸乙酯等酯类,N,N-二甲基甲酰胺、N,N-二甲基乙酰胺、N-甲基-2-吡咯烷酮等含氮类溶剂。上述溶剂可以单独使用一种,也可以两种或者两种以上混合使用,优选甲苯、二甲苯、均三甲苯等芳香族烃类溶剂与丙酮、丁酮、甲基乙基甲酮、甲基异丁基甲酮、环己酮等酮类熔剂混合使用。The solvent, as specific examples, alcohols such as methanol, ethanol, butanol, ethers such as ethyl cellosolve, butyl cellosolve, ethylene glycol-methyl ether, carbitol, butyl carbitol, etc. , acetone, butanone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone and other ketones, toluene, xylene, mesitylene and other aromatic hydrocarbons, ethoxy ethyl acetate, acetic acid Esters such as ethyl ester, nitrogen-containing solvents such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, etc. The above-mentioned solvents can be used alone or in combination of two or more, preferably aromatic hydrocarbon solvents such as toluene, xylene, mesitylene and acetone, butanone, methyl ethyl ketone, methyl iso Butyl ketone, cyclohexanone and other ketone solvents are used in combination.

本发明所述低粘度液体树脂的粘度为100~2000cps/25℃,优选200~1200cps/25℃,特别优选300~800cps/25℃。The viscosity of the low-viscosity liquid resin in the present invention is 100-2000cps/25°C, preferably 200-1200cps/25°C, particularly preferably 300-800cps/25°C.

所述低粘度液体树脂选自环氧树脂、丙烯酸树脂、有机硅树脂、不饱和聚酯树脂或聚氨酯树脂中的任意一种或者至少两种的混合物,所述混合物例如环氧树脂和丙烯酸树脂的混合物,有机硅树脂和不饱和聚酯树脂的混合物,不饱和聚酯树脂和聚氨酯树脂的混合物,环氧树脂、丙烯酸树脂和有机硅树脂的混合物,有机硅树脂、不饱和聚酯树脂和聚氨酯树脂的混合物,环氧树脂、丙烯酸树脂、有机硅树脂和不饱和聚酯树脂的混合物,优选环氧树脂和/或丙烯酸树脂,进一步优选环氧树脂和丙烯酸树脂,最优选环氧树脂。The low-viscosity liquid resin is selected from any one or a mixture of at least two of epoxy resins, acrylic resins, silicone resins, unsaturated polyester resins or polyurethane resins, such as the mixture of epoxy resins and acrylic resins Mixture, mixture of silicone resin and unsaturated polyester resin, mixture of unsaturated polyester resin and polyurethane resin, mixture of epoxy resin, acrylic resin and silicone resin, silicone resin, unsaturated polyester resin and polyurethane resin A mixture of epoxy resin, acrylic resin, silicone resin and unsaturated polyester resin, preferably epoxy resin and/or acrylic resin, more preferably epoxy resin and acrylic resin, most preferably epoxy resin.

优选地,所述环氧树脂优选缩水甘油醚环氧树脂或/和缩水甘油酯环氧树脂,进一步优选双酚A型环氧树脂、双酚F型环氧树脂、酚醛环氧树脂、甘油环氧树脂、四氢化苯二甲酯环氧树脂或邻苯二甲酯环氧树脂中的任意一种或者至少两种的混合物,最优选双酚A型环氧树脂。Preferably, the epoxy resin is preferably glycidyl ether epoxy resin or/and glycidyl ester epoxy resin, further preferably bisphenol A type epoxy resin, bisphenol F type epoxy resin, novolac epoxy resin, glycerol ring Oxygen resin, tetrahydrophthalic dimethyl ester epoxy resin or phthalic dimethyl ester epoxy resin, any one or a mixture of at least two, most preferably bisphenol A type epoxy resin.

优选地,所述双酚A型环氧树脂的环氧当量为180~280g/eq,优选185~210g/eq。Preferably, the epoxy equivalent of the bisphenol A epoxy resin is 180-280 g/eq, preferably 185-210 g/eq.

所述粉末涂料选自环氧粉末涂料、环氧-聚酯粉末涂料、聚酯粉末涂料、聚氨酯粉末涂料、丙烯酸粉末涂料或氟树脂粉末涂料中的任意一种或者至少两种的混合物,优选低温固化环氧粉末涂料、低温固化环氧-聚酯粉末涂料、低温固化聚酯粉末涂料、低温固化聚氨酯粉末涂料、低温固化丙烯酸粉末涂料或低温固化氟树脂粉末涂料中的任意一种或者至少两种的混合物,进一步优选低温固化环氧粉末涂料、低温固化环氧-聚酯粉末涂料或低温固化聚酯粉末涂料中的任意一种或者至少两种的混合物。所述“低温固化”是指固化温度低于140℃。上述低温固化粉末涂料可以市购得到,也可以参考现有技术中所公开的制备方法进行制备得到。The powder coating is selected from any one or a mixture of at least two of epoxy powder coatings, epoxy-polyester powder coatings, polyester powder coatings, polyurethane powder coatings, acrylic powder coatings or fluororesin powder coatings, preferably low temperature Any one or at least two of curing epoxy powder coatings, low temperature curing epoxy-polyester powder coatings, low temperature curing polyester powder coatings, low temperature curing polyurethane powder coatings, low temperature curing acrylic powder coatings or low temperature curing fluororesin powder coatings A mixture of, further preferably any one or a mixture of at least two of low temperature curing epoxy powder coatings, low temperature curing epoxy-polyester powder coatings or low temperature curing polyester powder coatings. The "low temperature curing" means that the curing temperature is lower than 140°C. The above-mentioned low-temperature curing powder coatings are commercially available, and can also be prepared by referring to the preparation methods disclosed in the prior art.

优选地,所述环氧粉末涂料、环氧-聚酯粉末涂料、低温固化环氧粉末涂料和低温固化环氧-聚酯粉末涂料中的环氧树脂为双酚A型环氧树脂,所述双酚A型环氧树脂的环氧当量为600~2000g/eq,优选600~1200g/eq。Preferably, the epoxy resin in the epoxy powder coating, epoxy-polyester powder coating, low-temperature curing epoxy powder coating and low-temperature curing epoxy-polyester powder coating is a bisphenol A type epoxy resin, and the The epoxy equivalent of the bisphenol A epoxy resin is 600-2000g/eq, preferably 600-1200g/eq.

优选地,所述环氧-聚酯粉末涂料、聚酯粉末涂料、低温固化环氧-聚酯粉末涂料和低温固化聚酯粉末涂料中的聚酯树脂为端羧基聚酯,所述端羧基聚酯的数均分子量为2000~9000,酸值为15~60,酸值优选为20~40。Preferably, the polyester resin in the epoxy-polyester powder coating, polyester powder coating, low-temperature curing epoxy-polyester powder coating and low-temperature curing polyester powder coating is carboxyl-terminated polyester, and the carboxyl-terminated polyester The number average molecular weight of the ester is 2000-9000, the acid value is 15-60, and the acid value is preferably 20-40.

所述丙烯酸粉末涂料和低温固化丙烯酸粉末涂料中的丙烯酸树脂为含有环氧基团的丙烯酸树脂,环氧当量为500~2200。The acrylic resin in the acrylic powder coating and the low-temperature curing acrylic powder coating is an acrylic resin containing epoxy groups, and the epoxy equivalent is 500-2200.

所述氟树脂粉末涂料和低温固化氟树脂粉末涂料中的氟树脂为羟基氟树脂,含氟量>20%,羟值为40~50mgKOH/g。The fluororesin in the fluororesin powder coating and the low-temperature curing fluororesin powder coating is a hydroxyl fluororesin with a fluorine content > 20% and a hydroxyl value of 40-50 mgKOH/g.

上述粉末涂料的组成以及制备方法均为已有技术,本领域技术人员可以市购得到,也可以根据现有技术中所公开的粉末涂料的组成以及方法进行制备得到。The composition and preparation method of the above-mentioned powder coatings are existing technologies, and those skilled in the art can obtain them from the market, or can be prepared according to the composition and methods of the powder coatings disclosed in the prior art.

将低粘度液体树脂组合物均匀涂敷在非导电基材表面,形成湿膜,控制湿膜的厚度为1~100μm,优选30~60μm。The low-viscosity liquid resin composition is evenly coated on the surface of the non-conductive substrate to form a wet film, and the thickness of the wet film is controlled to be 1-100 μm, preferably 30-60 μm.

对涂敷有低粘度液体树脂组合物的非导电基材喷涂粉末涂料,形成干膜,控制干膜厚度为10~200μm,优选20~50μm。Spraying a powder coating on the non-conductive substrate coated with the low-viscosity liquid resin composition to form a dry film, controlling the thickness of the dry film to be 10-200 μm, preferably 20-50 μm.

所述固化的温度为100~200℃,优选100~140℃;优选地,所述固化时间为10~60min,优选10~30min。The curing temperature is 100-200° C., preferably 100-140° C.; preferably, the curing time is 10-60 minutes, preferably 10-30 minutes.

一种非导电基材粉末涂料涂层的制备方法,包括如下步骤:A preparation method for a non-conductive substrate powder coating, comprising the steps of:

(1’)首先对非导电基材表面进行预处理,包括清理表面灰尘和污物、把粗糙表面磨平打光;(1') First, pre-treat the surface of the non-conductive substrate, including cleaning the surface dust and dirt, smoothing the rough surface;

(2’)将低粘度液体树脂组合物均匀涂覆于步骤(1’)处理过的非导电基材表面,形成湿膜,控制湿膜厚度为1~100μm,优选30~60μm;(2') Evenly coating the low-viscosity liquid resin composition on the surface of the non-conductive substrate treated in step (1') to form a wet film, controlling the thickness of the wet film to be 1-100 μm, preferably 30-60 μm;

(3’)对涂覆有低粘度液体树脂组合物的非导电基材喷涂粉末涂料,形成干膜,控制干膜厚度为10~200μm,优选20~50μm,然后加热固化,固化温度为100~200℃,优选100~140℃;固化时间为10~60min,优选10~30min,形成粉末涂层。(3') Spray powder coating on the non-conductive substrate coated with low-viscosity liquid resin composition to form a dry film, control the thickness of the dry film to be 10-200 μm, preferably 20-50 μm, and then heat and cure at a curing temperature of 100-200 μm 200°C, preferably 100~140°C; curing time is 10~60min, preferably 10~30min, to form a powder coating.

与现有技术相比,本发明具有如下有益效果:Compared with the prior art, the present invention has the following beneficial effects:

本发明所得涂料涂层厚度为5~200μm且可控,涂层表面光滑平整,涂层平整度≤3μm。相比于常用的静电喷涂,可用于非导电基材,且具有附着力好、节省能源、工艺简单等优点。The coating thickness of the coating obtained in the invention is 5-200 μm and controllable, the coating surface is smooth and flat, and the coating flatness is ≤3 μm. Compared with the commonly used electrostatic spraying, it can be used on non-conductive substrates, and has the advantages of good adhesion, energy saving, and simple process.

具体实施方式Detailed ways

为更好地说明本发明,便于理解本发明的技术方案,本发明的典型但非限制性的实施例如下:For better illustrating the present invention, facilitate understanding technical scheme of the present invention, typical but non-limiting embodiment of the present invention is as follows:

根据本发明所述方法在木材、塑料、玻璃、陶瓷、水泥等材料涂敷涂料涂层,附着力测试按照GB/T9286-1998测定,铅笔硬度测试按照GB/T6739-1996测定,厚度测试按照GB/T1764-1989测定。According to the method of the present invention, paint coatings are applied on materials such as wood, plastics, glass, ceramics, cement, etc., the adhesion test is measured according to GB/T9286-1998, the pencil hardness test is measured according to GB/T6739-1996, and the thickness test is measured according to GB/T9286-1996. /T1764-1989 determination.

实施例1:Example 1:

对50cm×50cm中密度纤维板进行表面预处理,清理表面灰尘和污物,用砂纸把粗糙表面磨平打光;将粘度为310cps,环氧当量为190g/eq的双酚A型环氧树脂及12%的BaxxodurTMEC301混合物作为底层底漆,将中密度纤维板放入涂胶机,调整涂胶机机器上部中间左右手轮,调节涂胶机的送料速度为15m/min,控制膜厚约为30μm,使其均匀涂覆在中密度纤维板上,检查无气泡、无孔洞后将涂覆好的板放入自动喷涂机内,调节喷涂速度为45m/min,往复喷涂,使粉末涂料均匀粘附在底漆上,厚度约为50μm。粉末涂料选用低温固化双酚A型环氧树脂粉末涂料(各组份用量见表1),然后放入110℃烘箱内固化30min。得到的涂层平整光滑,涂层平整度为3μm,无气孔针孔缩孔,涂膜附着力为0级,膜厚约为80μm,硬度为2H。Carry out surface pretreatment on 50cm×50cm medium density fiberboard, clean surface dust and dirt, smooth the rough surface with sandpaper; use bisphenol A type epoxy resin with a viscosity of 310cps and an epoxy equivalent of 190g/eq and 12 % Baxxodur TM EC301 mixture as the bottom primer, put the medium density fiberboard into the gluing machine, adjust the left and right hand wheels in the middle of the upper part of the gluing machine, adjust the feeding speed of the gluing machine to 15m/min, and control the film thickness to about 30μm. Make it evenly coated on the medium density fiberboard, check that there are no bubbles and no holes, put the coated board into the automatic spraying machine, adjust the spraying speed to 45m/min, and reciprocate spraying to make the powder coating evenly adhere to the bottom Paint, the thickness is about 50μm. The powder coating adopts low-temperature curing bisphenol A epoxy resin powder coating (see Table 1 for the dosage of each component), and then puts it into an oven at 110°C to cure for 30 minutes. The obtained coating is flat and smooth, with a coating flatness of 3 μm, no pores and pinhole shrinkage, a coating film adhesion of 0 grade, a film thickness of about 80 μm, and a hardness of 2H.

表1(重量份):Table 1 (parts by weight):

环氧树脂E-12Epoxy resin E-12 3535 聚酯树脂CE1099Polyester resin CE1099 1515 二甲基咪唑Dimethylimidazole 33 流平剂701Leveling agent 701 44 二氧化钛Titanium dioxide 4040 安息香Benzoin 33

实施例2:Example 2:

对50cm×50cm玻璃板进行表面预处理,清理表面灰尘和污物,将粘度为450cps的低粘度丙烯酸树脂及15%的TrigonoxV388混合物作为底层底漆,贮存于高位槽中,通过喷嘴从上方淋下30s,均匀玻璃板上,控制膜厚为45μm,使底漆均匀涂覆在玻璃板上,检查无气泡、无孔洞后将涂覆好的板放入自动喷涂机内,调节喷涂速度为30m/min,往复喷涂,使粉末涂料均匀粘附在底漆上,厚度约为85μm。粉末涂料选用丙烯酸粉末涂料(各组份用量见表2),然后放入140℃的烘箱内固化15min。得到的涂层平整光滑,涂层平整度为3μm,无气孔针孔缩孔,涂膜附着力为0级,膜厚为130μm,硬度为6H。Carry out surface pretreatment on the 50cm×50cm glass plate, clean the surface dust and dirt, use the mixture of low-viscosity acrylic resin with a viscosity of 450cps and 15% TrigonoxV388 as the bottom primer, store it in the high-level tank, and pour it from above through the nozzle 30s, evenly on the glass plate, control the film thickness to 45μm, so that the primer is evenly coated on the glass plate, check that there are no bubbles and no holes, put the coated plate into the automatic spraying machine, and adjust the spraying speed to 30m/ Min, reciprocating spraying, so that the powder coating is evenly adhered to the primer, and the thickness is about 85 μm. The powder coating is made of acrylic powder coating (see Table 2 for the dosage of each component), and then placed in an oven at 140°C for 15 minutes to cure. The obtained coating is flat and smooth, with a coating flatness of 3 μm, no pores and pinhole shrinkage, a coating film adhesion of grade 0, a film thickness of 130 μm, and a hardness of 6H.

表2(重量份):Table 2 (parts by weight):

丙烯酸树脂FB9870Acrylic resin FB9870 7070 封闭型多异氰酸酯blocked polyisocyanate 66

二丁基二月桂酸锡Dibutyltin dilaurate 1.51.5 流平剂701Leveling agent 701 11 二氧化钛Titanium dioxide 2020 氧化锌Zinc oxide 44 脱气蜡粉Degassed wax powder 55 安息香Benzoin 0.50.5

实施例3:Example 3:

对50cm×50cm塑料板进行表面预处理,清理表面灰尘和污物,将粘度为600cps,环氧当量为210g/eq的低粘度双酚A型环氧树脂作为底层底漆,将ABS板放入浸渍池浸渍5s后取出,使底漆均匀涂覆在塑料板上,厚度为65μm,检查无气泡、无孔洞后将涂覆好的板放入自动喷涂机内,调节喷涂速度为25m/min,往复喷涂,使粉末涂料均匀粘附在底漆上,厚度约为105μm。粉末涂料选用环氧粉末涂料(各组份用量见表3),然后放入110℃的烘箱内固化30分钟。得到的涂层平整光滑,涂层平整度为3μm,无气孔针孔缩孔,涂膜附着力为0级,膜厚为170μm,硬度为3H。Carry out surface pretreatment on the 50cm×50cm plastic board, clean the surface dust and dirt, use low viscosity bisphenol A type epoxy resin with a viscosity of 600cps and an epoxy equivalent of 210g/eq as the bottom primer, and put the ABS board into the After dipping in the dipping tank for 5s, take it out, so that the primer is evenly coated on the plastic plate, with a thickness of 65 μm. After checking that there are no bubbles and holes, put the coated plate into the automatic spraying machine, and adjust the spraying speed to 25m/min. Spray back and forth to make the powder coating evenly adhere to the primer, with a thickness of about 105 μm. The powder coating is made of epoxy powder coating (see Table 3 for the dosage of each component), and then placed in an oven at 110°C for 30 minutes to cure. The obtained coating is flat and smooth, with a coating flatness of 3 μm, no pores and pinhole shrinkage, a coating film adhesion of grade 0, a film thickness of 170 μm, and a hardness of 3H.

表3(重量份):Table 3 (parts by weight):

环氧树脂E-06Epoxy resin E-06 5555 癸二酸二酰肼sebacic acid dihydrazide 11 2-苯基咪唑啉2-Phenylimidazoline 1.51.5 流平剂701Leveling agent 701 33 碳酸钙calcium carbonate 2020 氧化锌Zinc oxide 2020

脱气蜡粉Degassed wax powder 11 安息香Benzoin 22

实施例4:Example 4:

对50cm×50cm陶瓷板进行表面预处理,清理表面灰尘和污物,将粘度为800cps的低粘度不饱和聚酯树脂作为底层底漆,将陶瓷板放入辊胶机,调整辊胶机机器上部中间左右手轮,调节辊胶机胶辊的速度为9m/min,控制膜厚为95μm,使底漆均匀涂覆在氧化锆陶瓷板上,检查无气泡、无孔洞后将涂覆好的板放入自动喷涂机内,调节喷涂速度为10m/min,往复喷涂,使粉末涂料均匀粘附在底漆上,厚度约为200μm。上层粉末涂料选用低温固化聚酯粉末涂料(各组份用量见表4),然后放入120℃的烘箱内固化25分钟。得到的涂层平整光滑,涂层平整度为2μm,无气孔针孔缩孔,涂膜附着力为0级,膜厚为395μm,硬度为3H。Carry out surface pretreatment on the 50cm×50cm ceramic plate, clean the surface dust and dirt, use low viscosity unsaturated polyester resin with a viscosity of 800cps as the bottom primer, put the ceramic plate into the roller gluer, and adjust the upper part of the roller gluer machine The left and right handwheels in the middle, adjust the speed of the rubber roller of the rubber machine to 9m/min, and control the film thickness to 95μm, so that the primer is evenly coated on the zirconia ceramic plate. After checking that there are no bubbles and no holes, put the coated plate Put it into the automatic spraying machine, adjust the spraying speed to 10m/min, and reciprocate spraying, so that the powder coating is evenly adhered to the primer, and the thickness is about 200μm. The upper powder coating is made of low-temperature curing polyester powder coating (see Table 4 for the dosage of each component), and then placed in an oven at 120°C for 25 minutes to cure. The obtained coating is flat and smooth, with a coating flatness of 2 μm, no pores and pinhole shrinkage, a coating film adhesion of 0 grade, a film thickness of 395 μm, and a hardness of 3H.

表4(重量份):Table 4 (parts by weight):

聚酯树脂XB1968-APolyester resin XB1968-A 6060 羟烷基酰胺Hydroxyalkylamides 55 醋酸丁酸纤维素Cellulose acetate butyrate 33 硫酸钡Barium sulfate 1515 氧化锌Zinc oxide 1515 脱气蜡粉Degassed wax powder 11 安息香Benzoin 11

实施例5:Example 5:

对50cm×50cm厚纸板进行表面预处理,清理表面灰尘和污物,将粘度为560cps的缩水甘油醚环氧树脂作为底层底漆,将厚纸板放入涂胶机,调整涂胶机机器上部中间左右手轮,调节涂胶机的送料速度为7m/min,控制膜厚为100μm,使底漆均匀涂覆在厚纸板上,检查无气泡、无孔洞后将涂覆好的板放入自动喷涂机内,调节喷涂速度为15m/min,往复喷涂,使粉末涂料均匀粘附在底漆上,厚度约为200μm。上层粉末涂料选用低温固化环氧-聚酯粉末涂料(各组份用量见表5),然后放入100℃的烘箱内固化20分钟。得到的涂层平整光滑,涂层平整度为3μm,无气孔针孔缩孔,涂膜附着力为0级,膜厚为340μm,硬度为2H。Carry out surface pretreatment on the 50cm×50cm thick cardboard, clean the surface dust and dirt, use glycidyl ether epoxy resin with a viscosity of 560cps as the bottom primer, put the thick cardboard into the gluing machine, and adjust the middle of the upper part of the gluing machine Left and right handwheels, adjust the feeding speed of the coating machine to 7m/min, control the film thickness to 100μm, so that the primer is evenly coated on the thick cardboard, check that there are no bubbles and no holes, and then put the coated board into the automatic spraying machine Inside, adjust the spraying speed to 15m/min, reciprocating spraying, so that the powder coating is evenly adhered to the primer, and the thickness is about 200μm. The upper layer powder coating is low-temperature curing epoxy-polyester powder coating (see Table 5 for the dosage of each component), and then placed in an oven at 100 ° C for 20 minutes to cure. The obtained coating is flat and smooth, with a coating flatness of 3 μm, no pores and pinhole shrinkage, a coating film adhesion of 0 grade, a film thickness of 340 μm, and a hardness of 2H.

表5(重量份):Table 5 (parts by weight):

聚酯树脂XB1968-CPolyester resin XB1968-C 4040 环氧树脂E-03Epoxy resin E-03 3434 2-甲基咪唑啉2-Methylimidazoline 22 流平剂503Leveling agent 503 22 硫酸钡Barium sulfate 1515 氧化锌Zinc oxide 55 脱气蜡粉Degassed wax powder 11 安息香Benzoin 11

实施例6Example 6

对50cm×50cm陶瓷板进行表面预处理,清理表面灰尘和污物,用砂纸把粗糙表面磨平打光;将粘度为100cps,环氧当量为180g/eq的双酚A型环氧树脂作为底层底漆,将陶瓷板放入涂胶机,调整涂胶机机器上部中间左右手轮,调节涂胶机的送料速度为15m/min,控制膜厚约为5μm,使其均匀涂覆在陶瓷板上,检查无气泡、无孔洞后将涂覆好的板放入自动喷涂机内,调节喷涂速度为45m/min,往复喷涂,使粉末涂料均匀粘附在底漆上,厚度约为20μm。粉末涂料选用低温固化双酚A型环氧树脂粉末涂料(各组份用量见表6),然后放入烘箱内在100℃固化30min。得到的涂层平整光滑,涂层平整度为3μm,无气孔针孔缩孔,涂膜附着力为0级,膜厚约为80μm,硬度为2H。Perform surface pretreatment on the 50cm×50cm ceramic plate, clean the surface dust and dirt, smooth the rough surface with sandpaper; use bisphenol A epoxy resin with a viscosity of 100cps and an epoxy equivalent of 180g/eq as the bottom layer Put the ceramic plate into the gluing machine, adjust the left and right hand wheels in the middle of the upper part of the gluing machine, adjust the feeding speed of the gluing machine to 15m/min, and control the film thickness to about 5μm, so that it can be evenly coated on the ceramic plate. After checking that there are no bubbles and no holes, put the coated board into the automatic spraying machine, adjust the spraying speed to 45m/min, and reciprocate spraying to make the powder coating evenly adhere to the primer, with a thickness of about 20μm. The powder coating adopts low-temperature curing bisphenol A epoxy resin powder coating (see Table 6 for the dosage of each component), and then puts it into an oven to cure at 100°C for 30 minutes. The obtained coating is flat and smooth, with a coating flatness of 3 μm, no pores and pinhole shrinkage, a coating film adhesion of grade 0, a film thickness of about 80 μm, and a hardness of 2H.

表6(重量份):Table 6 (parts by weight):

环氧树脂E-12Epoxy resin E-12 3535 聚酯树脂CE1099Polyester resin CE1099 1515 二甲基咪唑Dimethylimidazole 33 流平剂701Leveling agent 701 44 二氧化钛Titanium dioxide 4040 安息香Benzoin 33

实施例7Example 7

对50cm×50cm玻璃板进行表面预处理,清理表面灰尘和污物,用砂纸把粗糙表面磨平打光;将粘度为2000cps,环氧当量为280g/eq的双酚A型环氧树脂作为底层底漆,将玻璃板放入涂胶机,调整涂胶机机器上部中间左右手轮,调节涂胶机的送料速度为15m/min,控制膜厚约为100μm,使其均匀涂覆在玻璃板上,检查无气泡、无孔洞后将涂覆好的板放入自动喷涂机内,调节喷涂速度为45m/min,往复喷涂,使粉末涂料均匀粘附在底漆上,厚度约为150μm。粉末涂料选用双酚A型环氧树脂粉末涂料,所述双酚A型环氧树脂的环氧当量为600g/eq,各组份用量见表7,然后放入烘箱内在200℃固化60min。得到的涂层平整光滑,涂层平整度为5μm,无气孔针孔缩孔,涂膜附着力为0级,膜厚约为80μm,硬度为2H。Carry out surface pretreatment on the 50cm×50cm glass plate, clean the surface dust and dirt, and smooth the rough surface with sandpaper; use bisphenol A epoxy resin with a viscosity of 2000cps and an epoxy equivalent of 280g/eq as the bottom layer Put the glass plate into the glue coating machine, adjust the left and right hand wheels in the middle of the upper part of the glue coating machine, adjust the feeding speed of the glue coating machine to 15m/min, and control the film thickness to about 100μm, so that it can be evenly coated on the glass plate. After checking that there are no bubbles and no holes, put the coated board into the automatic spraying machine, adjust the spraying speed to 45m/min, and reciprocate spraying to make the powder coating evenly adhere to the primer, with a thickness of about 150μm. Bisphenol A type epoxy resin powder coating is selected as the powder coating. The epoxy equivalent of the bisphenol A type epoxy resin is 600g/eq. The dosage of each component is shown in Table 7, and then put into an oven and cured at 200°C for 60min. The obtained coating is flat and smooth, with a coating flatness of 5 μm, no pores and pinhole shrinkage, a coating adhesion of grade 0, a film thickness of about 80 μm, and a hardness of 2H.

表7(重量份):Table 7 (parts by weight):

双酚A型环氧树脂Bisphenol A type epoxy resin 5555 癸二酸二酰肼sebacic acid dihydrazide 11 2-苯基咪唑啉2-Phenylimidazoline 1.51.5 流平剂701Leveling agent 701 33 碳酸钙calcium carbonate 2020 氧化锌Zinc oxide 2020 脱气蜡粉Degassed wax powder 11 安息香Benzoin 22

实施例8Example 8

对50cm×50cm陶瓷板进行表面预处理,清理表面灰尘和污物,用砂纸把粗糙表面磨平打光;将粘度为1200cps,环氧当量为230g/eq的双酚A型环氧树脂作为底层底漆,将陶瓷板放入涂胶机,调整涂胶机机器上部中间左右手轮,调节涂胶机的送料速度为15m/min,控制膜厚约为50μm,使其均匀涂覆在陶瓷板上,检查无气泡、无孔洞后将涂覆好的板放入自动喷涂机内,调节喷涂速度为45m/min,往复喷涂,使粉末涂料均匀粘附在底漆上,厚度约为200μm。粉末涂料选用双酚A型环氧树脂粉末涂料,所述双酚A型环氧树脂的环氧当量为2000g/eq,各组份用量见表8,然后放入烘箱内在150℃固化40min。得到的涂层平整光滑,涂层平整度为5μm,无气孔针孔缩孔,涂膜附着力为0级,膜厚约为80μm,硬度为2H。Carry out surface pretreatment on the 50cm×50cm ceramic plate, clean the surface dust and dirt, and smooth the rough surface with sandpaper; use bisphenol A epoxy resin with a viscosity of 1200cps and an epoxy equivalent of 230g/eq as the bottom layer Put the ceramic plate into the gluing machine, adjust the left and right hand wheels in the middle of the upper part of the gluing machine, adjust the feeding speed of the gluing machine to 15m/min, and control the film thickness to about 50μm, so that it can be evenly coated on the ceramic plate. After checking that there are no bubbles and no holes, put the coated board into the automatic spraying machine, adjust the spraying speed to 45m/min, and reciprocate spraying to make the powder coating evenly adhere to the primer, with a thickness of about 200μm. Bisphenol A type epoxy resin powder coating is selected as the powder coating. The epoxy equivalent of the bisphenol A type epoxy resin is 2000g/eq. The dosage of each component is shown in Table 8, and then put into an oven and cured at 150°C for 40min. The obtained coating is flat and smooth, with a coating flatness of 5 μm, no pores and pinhole shrinkage, a coating adhesion of grade 0, a film thickness of about 80 μm, and a hardness of 2H.

表8(重量份):Table 8 (parts by weight):

双酚A型环氧树脂Bisphenol A type epoxy resin 5555 癸二酸二酰肼sebacic acid dihydrazide 11

2-苯基咪唑啉2-Phenylimidazoline 1.51.5 流平剂701Leveling agent 701 33 碳酸钙calcium carbonate 2020 氧化锌Zinc oxide 2020 脱气蜡粉Degassed wax powder 11 安息香Benzoin 22

实施例9Example 9

对50cm×50cm的ABS板材进行表面预处理,清理表面灰尘和污物,将粘度为560cps的双酚F型环氧树脂作为底层底漆,将ABS板材放入涂胶机,调整涂胶机机器上部中间左右手轮,调节涂胶机的送料速度为7m/min,控制膜厚为100μm,使底漆均匀涂覆在厚纸板上,检查无气泡、无孔洞后将涂覆好的ABS板放入自动喷涂机内,调节喷涂速度为15m/min,往复喷涂,使粉末涂料均匀粘附在底漆上,厚度约为140μm。上层粉末涂料选用低温固化聚酯粉末涂料,端羧基聚酯的数均分子量为2000~9000,酸值为15,各组份用量见表9,然后放入120℃的烘箱内固化40分钟。得到的涂层平整光滑,涂层平整度为3μm,无气孔针孔缩孔,涂膜附着力为0级,膜厚为340μm,硬度为2H。Perform surface pretreatment on the 50cm×50cm ABS plate, clean the surface dust and dirt, use bisphenol F epoxy resin with a viscosity of 560cps as the bottom primer, put the ABS plate into the gluing machine, and adjust the gluing machine The left and right hand wheels in the middle of the upper part, adjust the feeding speed of the glue applicator to 7m/min, and control the film thickness to 100μm, so that the primer is evenly coated on the cardboard. After checking that there are no bubbles and holes, put the coated ABS board into the In the automatic spraying machine, adjust the spraying speed to 15m/min, and reciprocate spraying, so that the powder coating is evenly adhered to the primer, and the thickness is about 140μm. The upper layer powder coating adopts low-temperature curing polyester powder coating. The number average molecular weight of the carboxyl-terminated polyester is 2000~9000, and the acid value is 15. The dosage of each component is shown in Table 9, and then placed in an oven at 120 ° C for 40 minutes to cure. The obtained coating is flat and smooth, with a coating flatness of 3 μm, no pores and pinhole shrinkage, a coating film adhesion of 0 grade, a film thickness of 340 μm, and a hardness of 2H.

表9(重量份):Table 9 (parts by weight):

端羧基聚酯Carboxy-terminated polyester 120120 HAA固化剂HAA curing agent 1515 流平剂503Leveling agent 503 22 硫酸钡Barium sulfate 1515 氧化锌Zinc oxide 55 脱气蜡粉Degassed wax powder 11

安息香Benzoin 11

实施例10Example 10

对50cm×50cm的水泥板进行表面预处理,清理表面灰尘和污物,将粘度为700cps的有机硅树脂作为底层底漆,将水泥板放入涂胶机,调整涂胶机机器上部中间左右手轮,调节涂胶机的送料速度为7m/min,控制膜厚为600μm,使底漆均匀涂覆在厚纸板上,检查无气泡、无孔洞后将涂覆好的水泥板放入自动喷涂机内,调节喷涂速度为15m/min,往复喷涂,使粉末涂料均匀粘附在底漆上,厚度约为150μm。上层粉末涂料选用低温固化聚酯粉末涂料,端羧基聚酯的数均分子量为2000~9000,酸值为60,各组份用量见表10,然后放入120℃的烘箱内固化40分钟。得到的涂层平整光滑,涂层平整度为3μm,无气孔针孔缩孔,涂膜附着力为0级,膜厚为340μm,硬度为2H。Carry out surface pretreatment on the 50cm×50cm cement board, clean the surface dust and dirt, use the silicone resin with a viscosity of 700cps as the bottom primer, put the cement board into the glue applicator, adjust the left and right handwheels in the middle of the upper part of the glue applicator , adjust the feeding speed of the coating machine to 7m/min, control the film thickness to 600μm, so that the primer is evenly coated on the cardboard, check that there are no bubbles and no holes, and then put the coated cement board into the automatic spraying machine , adjust the spraying speed to 15m/min, reciprocating spraying, so that the powder coating is evenly adhered to the primer, and the thickness is about 150μm. The upper layer powder coating is made of low-temperature curing polyester powder coating. The number average molecular weight of the carboxyl-terminated polyester is 2000~9000, and the acid value is 60. The dosage of each component is shown in Table 10, and then placed in an oven at 120 ° C for 40 minutes to cure. The obtained coating is flat and smooth, with a coating flatness of 3 μm, no pores and pinhole shrinkage, a coating film adhesion of 0 grade, a film thickness of 340 μm, and a hardness of 2H.

表10(重量份):Table 10 (parts by weight):

端羧基聚酯Carboxy-terminated polyester 120120 HAA固化剂HAA curing agent 1515 流平剂503Leveling agent 503 22 硫酸钡Barium sulfate 1515 氧化锌Zinc oxide 55 脱气蜡粉Degassed wax powder 11 安息香Benzoin 11

实施例11Example 11

对50cm×50cm陶瓷板进行表面预处理,清理表面灰尘和污物,将粘度为200cps的低粘度聚氨酯树脂作为底层底漆,将陶瓷板放入辊胶机,调整辊胶机机器上部中间左右手轮,调节辊胶机胶辊的速度为9m/min,控制膜厚为95μm,使底漆均匀涂覆在陶瓷板上,检查无气泡、无孔洞后将涂覆好的板放入自动喷涂机内,调节喷涂速度为10m/min,往复喷涂,使粉末涂料均匀粘附在底漆上,厚度约为160μm。上层粉末涂料选用丙烯酸粉末涂料,所述丙烯酸粉末涂料中的丙烯酸树脂为含有环氧基团的丙烯酸树脂,环氧当量为500g/eq,(各组份用量见表11),然后放入120℃的烘箱内固化25分钟。得到的涂层平整光滑,涂层平整度为2μm,无气孔针孔缩孔,涂膜附着力为0级,膜厚为395μm,硬度为3H。Carry out surface pretreatment on the 50cm×50cm ceramic plate, clean the dust and dirt on the surface, use low-viscosity polyurethane resin with a viscosity of 200cps as the bottom primer, put the ceramic plate into the roller gluer, and adjust the left and right handwheels in the upper middle of the roller gluer machine , adjust the speed of the rubber roller of the roller rubber machine to 9m/min, and control the film thickness to 95μm, so that the primer is evenly coated on the ceramic plate, and after checking that there are no bubbles and holes, put the coated plate into the automatic spraying machine , adjust the spraying speed to 10m/min, reciprocating spraying, so that the powder coating is evenly adhered to the primer, and the thickness is about 160μm. The upper powder coating is made of acrylic powder coating. The acrylic resin in the acrylic powder coating is an acrylic resin containing epoxy groups, and the epoxy equivalent is 500g/eq (see Table 11 for the dosage of each component). Cured in the oven for 25 minutes. The obtained coating was flat and smooth, with a coating flatness of 2 μm, no pores and pinhole shrinkage, a coating film adhesion of grade 0, a film thickness of 395 μm, and a hardness of 3H.

表11(重量份):Table 11 (parts by weight):

丙烯酸树脂Acrylic 8585 己二酸Adipic acid 1010 流平剂701Leveling agent 701 11 环氧树脂E-16Epoxy resin E-16 3.53.5 安息香Benzoin 0.50.5

实施例12Example 12

对50cm×50cm陶瓷板进行表面预处理,清理表面灰尘和污物,将粘度为200cps的低粘度聚氨酯树脂作为底层底漆,将陶瓷板放入辊胶机,调整辊胶机机器上部中间左右手轮,调节辊胶机胶辊的速度为9m/min,控制膜厚为95μm,使底漆均匀涂覆在陶瓷板上,检查无气泡、无孔洞后将涂覆好的板放入自动喷涂机内,调节喷涂速度为10m/min,往复喷涂,使粉末涂料均匀粘附在底漆上,厚度约为180μm。上层粉末涂料选用丙烯酸粉末涂料,所述丙烯酸粉末涂料中的丙烯酸树脂为含有环氧基团的丙烯酸树脂,环氧当量为2200g/eq,(各组份用量见表11),然后放入120℃的烘箱内固化25分钟。得到的涂层平整光滑,涂层平整度为2μm,无气孔针孔缩孔,涂膜附着力为0级,膜厚为395μm,硬度为3H。Carry out surface pretreatment on the 50cm×50cm ceramic plate, clean the dust and dirt on the surface, use low-viscosity polyurethane resin with a viscosity of 200cps as the bottom primer, put the ceramic plate into the roller gluer, and adjust the left and right handwheels in the upper middle of the roller gluer machine , adjust the speed of the rubber roller of the roller rubber machine to 9m/min, and control the film thickness to 95μm, so that the primer is evenly coated on the ceramic plate, and after checking that there are no bubbles and holes, put the coated plate into the automatic spraying machine , adjust the spraying speed to 10m/min, reciprocating spraying, so that the powder coating is evenly adhered to the primer, and the thickness is about 180μm. The upper layer powder coating is made of acrylic powder coating. The acrylic resin in the acrylic powder coating is an acrylic resin containing epoxy groups, and the epoxy equivalent is 2200g/eq (see Table 11 for the dosage of each component). Cured in the oven for 25 minutes. The obtained coating was flat and smooth, with a coating flatness of 2 μm, no pores and pinhole shrinkage, a coating film adhesion of grade 0, a film thickness of 395 μm, and a hardness of 3H.

表12(重量份):Table 12 (parts by weight):

丙烯酸树脂Acrylic 8585 十二碳二羧酸dodecanedicarboxylic acid 1010 流平剂503Leveling agent 503 11 环氧树脂E-16Epoxy resin E-16 3.53.5 安息香Benzoin 0.50.5

实施例13Example 13

对50cm×50cmABS板进行表面预处理,清理表面灰尘和污物,将粘度为600cps,环氧当量为210g/eq的低粘度双酚A型环氧树脂作为底层底漆,将ABS板放入浸渍池浸渍5s后取出,使底漆均匀涂覆在塑料板上,厚度为65μm,检查无气泡、无孔洞后将涂覆好的ABS板放入自动喷涂机内,调节喷涂速度为25m/min,往复喷涂,使粉末涂料均匀粘附在底漆上,厚度约为105μm。粉末涂料选用氟树脂粉末涂料,所述氟树脂粉末涂料中的氟树脂为羟基氟树脂,含氟量大于20%,羟值为40mgKOH/g,各组份用量见表13,然后放入110℃的烘箱内固化30分钟。得到的涂层平整光滑,涂层平整度为3μm,无气孔针孔缩孔,涂膜附着力为0级,膜厚为170μm,硬度为3H。Perform surface pretreatment on the 50cm×50cm ABS board, clean the surface dust and dirt, use low viscosity bisphenol A epoxy resin with a viscosity of 600cps and an epoxy equivalent of 210g/eq as the bottom primer, and put the ABS board into the dipping Take it out after dipping in the pool for 5s, so that the primer is evenly coated on the plastic plate with a thickness of 65 μm. After checking that there are no bubbles and no holes, put the coated ABS plate into the automatic spraying machine, and adjust the spraying speed to 25m/min. Spray back and forth to make the powder coating evenly adhere to the primer, with a thickness of about 105 μm. The powder coating is made of fluororesin powder coating. The fluororesin in the fluororesin powder coating is hydroxyl fluororesin, the fluorine content is greater than 20%, and the hydroxyl value is 40mgKOH/g. Cured in the oven for 30 minutes. The obtained coating is flat and smooth, with a coating flatness of 3 μm, no pores and pinhole shrinkage, a coating film adhesion of grade 0, a film thickness of 170 μm, and a hardness of 3H.

表13(重量份):Table 13 (parts by weight):

羟基氟树脂Hydroxy Fluorine Resin 6868 封闭型异佛尔酮异氰酸酯Blocked isophorone isocyanate 1515

流平剂701Leveling agent 701 11 二氧化钛Titanium dioxide 1515 安息香Benzoin 11

实施例14Example 14

对50cm×50cmABS进行表面预处理,清理表面灰尘和污物,将粘度为600cps,环氧当量为210g/eq的低粘度双酚A型环氧树脂作为底层底漆,将ABS板放入浸渍池浸渍5s后取出,使底漆均匀涂覆在塑料板上,厚度为65μm,检查无气泡、无孔洞后将涂覆好的ABS板放入自动喷涂机内,调节喷涂速度为25m/min,往复喷涂,使粉末涂料均匀粘附在底漆上,厚度约为105μm。粉末涂料选用氟树脂粉末涂料,所述氟树脂粉末涂料中的氟树脂为羟基氟树脂,含氟量大于20%,羟值为50mgKOH/g,各组份用量见表14,然后放入110℃的烘箱内固化30分钟。得到的涂层平整光滑,涂层平整度为3μm,无气孔针孔缩孔,涂膜附着力为0级,膜厚为170μm,硬度为3H。Perform surface pretreatment on 50cm×50cmABS, clean surface dust and dirt, use low-viscosity bisphenol A epoxy resin with a viscosity of 600cps and an epoxy equivalent of 210g/eq as the bottom primer, and put the ABS board into the dipping tank Take it out after dipping for 5s, so that the primer is evenly coated on the plastic plate with a thickness of 65 μm. After checking that there are no bubbles and no holes, put the coated ABS plate into the automatic spraying machine, adjust the spraying speed to 25m/min, reciprocate Spray to make the powder coating evenly adhere to the primer, the thickness is about 105μm. The powder coating is made of fluororesin powder coating. The fluororesin in the fluororesin powder coating is hydroxyl fluororesin, the fluorine content is greater than 20%, and the hydroxyl value is 50mgKOH/g. Cured in the oven for 30 minutes. The obtained coating is flat and smooth, with a coating flatness of 3 μm, no pores and pinhole shrinkage, a coating film adhesion of grade 0, a film thickness of 170 μm, and a hardness of 3H.

表14(重量份):Table 14 (parts by weight):

羟基氟树脂Hydroxy Fluorine Resin 6363 封闭型异佛尔酮异氰酸酯Blocked isophorone isocyanate 1515 流平剂503Leveling agent 503 11 二氧化钛Titanium dioxide 2020 安息香Benzoin 11

应该注意到并理解,在不脱离后附的权利要求所要求的本发明的精神和范围的情况下,能够对上述详细描述的本发明做出各种修改和改进。因此,要求保护的技术方案的范围不受所给出的任何特定示范教导的限制。It should be noted and understood that various modifications and improvements can be made to the invention described in detail above without departing from the spirit and scope of the invention as claimed in the appended claims. Accordingly, the scope of the claimed technical solution is not limited by any particular exemplary teaching given.

申请人声明,本发明通过上述实施例来说明本发明的详细方法,但本发明并不局限于上述详细方法,即不意味着本发明必须依赖上述详细方法才能实施。所属技术领域的技术人员应该明了,对本发明的任何改进,对本发明产品各原料的等效替换及辅助成分的添加、具体方式的选择等,均落在本发明的保护范围和公开范围之内。The applicant declares that the present invention illustrates the detailed methods of the present invention through the above-mentioned examples, but the present invention is not limited to the above-mentioned detailed methods, that is, it does not mean that the present invention can only be implemented depending on the above-mentioned detailed methods. Those skilled in the art should understand that any improvement of the present invention, the equivalent replacement of each raw material of the product of the present invention, the addition of auxiliary components, the selection of specific methods, etc., all fall within the scope of protection and disclosure of the present invention.

Claims (31)

1. a preparation method for non-conductive substrate powder paint coating, is characterized in that, described method comprises the steps:
(1) to non-conductive substrate coating low-viscosity (mobile) liquid resin combination, described low-viscosity (mobile) liquid resin combination is selected from the combination of any one or at least two kinds in the mixture of the mixture of low-viscosity (mobile) liquid resin, low-viscosity (mobile) liquid resin and solvent, low-viscosity (mobile) liquid resin and curing agent, and the viscosity of described low-viscosity (mobile) liquid resin is 100 ~ 2000cps/25 DEG C;
(2) to the non-conductive substrate spray coating powder paint being coated with low-viscosity (mobile) liquid resin combination, be heating and curing, form powder coating;
Wherein, by low-viscosity (mobile) liquid resin combination even application on non-conductive substrate surface, wet film is formed, the thickness controlling wet film is 1 ~ 100 μm, to the non-conductive substrate spray coating powder paint being coated with low-viscosity (mobile) liquid resin combination, form dry film, controlling build is 10 ~ 200 μm.
2. the method for claim 1, is characterized in that, step (1) is front carries out pretreatment to non-conductive substrate surface, and described pretreatment comprises cleaning non-conductive substrate surface dirt and dirt, and rough surface is polished polishing.
3. method as claimed in claim 1 or 2, is characterized in that, described non-conductive substrate is selected from the mixture of any one or at least two kinds in timber, paper, cement, glass, plastics or pottery.
4. method as claimed in claim 3, it is characterized in that, described non-conductive substrate is selected from timber.
5. the method for claim 1, is characterized in that, the viscosity of described low-viscosity (mobile) liquid resin is 200 ~ 1200cps/25 DEG C.
6. method as claimed in claim 5, it is characterized in that, the viscosity of described low-viscosity (mobile) liquid resin is 300 ~ 800cps/25 DEG C.
7. the method for claim 1, is characterized in that, described low-viscosity (mobile) liquid resin is selected from the mixture of any one or at least two kinds in epoxy resin, acrylic resin, organic siliconresin, unsaturated polyester resin or polyurethane resin.
8. method as claimed in claim 7, it is characterized in that, described low-viscosity (mobile) liquid resin is selected from epoxy resin and/or acrylic resin.
9. method as claimed in claim 8, it is characterized in that, described low-viscosity (mobile) liquid resin is selected from epoxy resin and acrylic resin.
10. method as claimed in claim 7, it is characterized in that, described low-viscosity (mobile) liquid resin is selected from epoxy resin.
11. methods as claimed in claim 7, is characterized in that, described epoxy resin is that tetraglycidel ether epoxy resin is or/and ethylene oxidic ester epoxy resin.
12. methods as claimed in claim 11, it is characterized in that, described epoxy resin is the mixture of any one or at least two kinds in bisphenol A type epoxy resin, bisphenol f type epoxy resin, novolac epoxy resin, glycerol epoxy resin, tetrahydrobenzene dimethyl ester epoxy resin or O-phthalic ester epoxy resin.
13. methods as claimed in claim 12, it is characterized in that, described epoxy resin is bisphenol A type epoxy resin.
14. methods as claimed in claim 13, is characterized in that, the epoxide equivalent of described bisphenol A type epoxy resin is 180 ~ 280g/eq.
15. methods as claimed in claim 14, is characterized in that, the epoxide equivalent of described bisphenol A type epoxy resin is 185 ~ 210g/eq.
16. the method for claim 1, it is characterized in that, described powdery paints is selected from the mixture of any one or at least two kinds in epoxide powder coating, epoxy-polyester powder coating, polyester powder coating, polyurethane powder coating, acrylic acid powder coatings or fluororesin powder coating.
17. methods as claimed in claim 16, it is characterized in that, described powdery paints is selected from the mixture of any one or at least two kinds in Low-Temperature Curable Epoxy Powder Paint, temperature curing epoxy low-polyester powder coating, low-temperature setting polyester powder coating, low-temperature setting polyurethane powder coating, low-temperature setting acrylic acid powder coatings or low-temperature setting fluororesin powder coating, and described low-temperature setting refers to that solidification temperature is lower than 140 DEG C.
18. methods as claimed in claim 17, is characterized in that, described powdery paints is selected from the mixture of any one or at least two kinds in Low-Temperature Curable Epoxy Powder Paint, temperature curing epoxy low-polyester powder coating or low-temperature setting polyester powder coating.
19. methods as claimed in claim 17, it is characterized in that, epoxy resin in Low-Temperature Curable Epoxy Powder Paint and temperature curing epoxy low-polyester powder coating is bisphenol A type epoxy resin, and the epoxide equivalent of described bisphenol A type epoxy resin is 600 ~ 2000g/eq.
20. methods as claimed in claim 19, is characterized in that, the epoxide equivalent of described bisphenol A type epoxy resin is 600 ~ 1200g/eq.
21. methods as claimed in claim 17, it is characterized in that, mylar in described temperature curing epoxy low-polyester powder coating and low-temperature setting polyester powder coating is terminal carboxyl polyester, and the number-average molecular weight of described terminal carboxyl polyester is 2000 ~ 9000, and acid number is 15 ~ 60.
22. methods as claimed in claim 21, it is characterized in that, acid number is 20 ~ 40.
23. methods as claimed in claim 17, is characterized in that, the acrylic resin in described low-temperature setting acrylic acid powder coatings is the acrylic resin containing epoxide group, and epoxide equivalent is 500 ~ 2200g/eq.
24. methods as claimed in claim 17, is characterized in that, the fluororesin in described low-temperature setting fluororesin powder coating is hydroxyl fluororesin, fluorinated volume > 20%, and hydroxyl value is 40 ~ 50mgKOH/g.
25. the method for claim 1, is characterized in that, by low-viscosity (mobile) liquid resin combination even application on non-conductive substrate surface, form wet film, the thickness controlling wet film is 30 ~ 60 μm.
26. the method for claim 1, is characterized in that, to the non-conductive substrate spray coating powder paint being coated with low-viscosity (mobile) liquid resin combination, form dry film, controlling build is 20 ~ 50 μm.
27. the method for claim 1, is characterized in that, the temperature of described solidification is 100 ~ 200 DEG C.
28. methods as claimed in claim 27, is characterized in that, the temperature of described solidification is 100 ~ 140 DEG C.
29. the method for claim 1, is characterized in that, described hardening time is 10 ~ 60min.
30. methods as claimed in claim 29, it is characterized in that, described hardening time is 10 ~ 30min.
31. the method for claim 1, is characterized in that, described method comprises the steps:
(1 ') first carries out pretreatment to non-conductive substrate surface, comprises cleaning surface dirt and dirt, rough surface is polished polishing;
Low-viscosity (mobile) liquid resin combination is evenly coated on the non-conductive substrate surface that step (1 ') processed by (2 '), and form wet film, controlling wet-film thickness is 1 ~ 100 μm;
(3 '), to the non-conductive substrate spray coating powder paint being coated with low-viscosity (mobile) liquid resin combination, forms dry film, and controlling build is 10 ~ 200 μm, and be then heating and curing, solidification temperature is 100 ~ 200 DEG C; Hardening time is 10 ~ 60min, forms powder coating.
CN201210537047.2A 2012-12-12 2012-12-12 A kind of preparation method of non-conductive substrate powder paint coating Active CN103031014B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201210537047.2A CN103031014B (en) 2012-12-12 2012-12-12 A kind of preparation method of non-conductive substrate powder paint coating

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201210537047.2A CN103031014B (en) 2012-12-12 2012-12-12 A kind of preparation method of non-conductive substrate powder paint coating

Publications (2)

Publication Number Publication Date
CN103031014A CN103031014A (en) 2013-04-10
CN103031014B true CN103031014B (en) 2015-11-18

Family

ID=48018435

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201210537047.2A Active CN103031014B (en) 2012-12-12 2012-12-12 A kind of preparation method of non-conductive substrate powder paint coating

Country Status (1)

Country Link
CN (1) CN103031014B (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104231686B (en) * 2014-08-22 2016-07-06 安徽博大纤维素科技有限公司 A kind of powdery paints of long service life
CN104588301A (en) * 2015-02-15 2015-05-06 浙江省磐安县绿海工艺厂有限公司 Powder coating method for surface of bamboo and wood material
CN104889039A (en) * 2015-06-04 2015-09-09 遵义春华新材料科技有限公司 Powder coating applying process of non-conductor substrate
CN106311565A (en) * 2015-06-30 2017-01-11 富钰精密组件(昆山)有限公司 Electrostatic spraying method for complex of metal and non-conducting material and shell
CN105542631A (en) * 2016-01-28 2016-05-04 廊坊云途科技有限公司 Special transparent powder coating for glass plate and preparation and use method thereof
NL2019197B1 (en) * 2017-07-07 2019-01-16 Stahl Int B V Powder coating method and coated article
CN107938375A (en) * 2017-12-22 2018-04-20 湖北金龙新材料股份有限公司 A kind of processing method of the paste polyvinyl chloride cloth with thermoplastic polyurethane coating
CN108531056B (en) * 2018-04-03 2020-06-09 中国科学院过程工程研究所 Heat-sensitive substrate powder coating and preparation method thereof
CN113316401B (en) * 2019-12-20 2023-07-21 株式会社爱世克私 Shoe upper manufacturing method, shoe upper and shoe
CN113122103A (en) * 2019-12-30 2021-07-16 苏州青田新材料有限公司 Imitation electroplating powder coating and preparation method thereof
CN111554882A (en) * 2020-05-13 2020-08-18 中科(马鞍山)新材料科创园有限公司 Ternary positive pole piece and coating method and application thereof
CN112495735A (en) * 2020-11-04 2021-03-16 西安鑫垚陶瓷复合材料有限公司 Surface flatness processing method for ceramic matrix composite material satellite light structural part and structural part
CN112724803B (en) * 2020-12-29 2022-06-07 老虎表面技术新材料(苏州)有限公司 Plane powder coating composition and coating thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1291220A (en) * 1998-02-17 2001-04-11 纳幕尔杜邦公司 Method for forming powder coatings
CN1382074A (en) * 1999-10-28 2002-11-27 温莎技术有限公司 Method of applying powder coating to non-metallic substrate
CN1426854A (en) * 2001-12-21 2003-07-02 日本油漆株式会社 Method for forming coated film on metal material and coated object thereof
CN101720345A (en) * 2007-07-02 2010-06-02 阿克苏·诺贝尔粉末涂料(宁波)有限公司 Powder coating composition for high temperature resistant coatings

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1291220A (en) * 1998-02-17 2001-04-11 纳幕尔杜邦公司 Method for forming powder coatings
CN1382074A (en) * 1999-10-28 2002-11-27 温莎技术有限公司 Method of applying powder coating to non-metallic substrate
CN1426854A (en) * 2001-12-21 2003-07-02 日本油漆株式会社 Method for forming coated film on metal material and coated object thereof
CN101720345A (en) * 2007-07-02 2010-06-02 阿克苏·诺贝尔粉末涂料(宁波)有限公司 Powder coating composition for high temperature resistant coatings

Also Published As

Publication number Publication date
CN103031014A (en) 2013-04-10

Similar Documents

Publication Publication Date Title
CN103031014B (en) A kind of preparation method of non-conductive substrate powder paint coating
JP5699307B2 (en) Film formation method
CN104559741A (en) UV (ultraviolet) finishing varnish for laser roller coating
MY149319A (en) Multilayer coating film-forming method
JP2016087569A5 (en)
CN106675378A (en) Waterborne UV matt varnish
US20140349028A1 (en) Precoating methods and compositions
CN103059718B (en) Ultraviolet light cured three-dimensional magic paint
CN108501133A (en) PVC faced plywood and its making method
CN109957319A (en) A kind of ultraviolet light cured burnished real color finishing coat of environmental protection high efficiency water for furniture
CN105017954B (en) Automobile coating bottom is made up the difference agent and automobile finish restorative procedure
CN103232752A (en) Screen printing ink for UV (ultraviolet) paint surface and preparation method thereof
CN107791632A (en) A kind of antiradar reflectivity of TAC base materials is without rainbow line hardening diaphragm and preparation method thereof
CN106634543A (en) UV roller-coating adhesion white primer
CN108531056B (en) Heat-sensitive substrate powder coating and preparation method thereof
US20100040841A1 (en) Web-like coating film
CN106700855A (en) Ultraviolet light solidification transparent adhesive force priming paint using in bathrooms
JP3198159B2 (en) Coating composition
US20250170610A1 (en) Process for applying coating compositions having different leveling properties and/or sag resistance to different target areas of an object
CN103182371A (en) Construction machinery and painting process thereof
US20250170599A1 (en) Process for producing a coated object comprising coating layers having adjustable properties
JPS583752B2 (en) Tosouhouhou
JPH0558791B2 (en)
JP4170252B2 (en) Water-based colored paint, painted product, and method for producing painted product
JP2008246710A (en) Decorative sheet and method for producing the same

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
TR01 Transfer of patent right

Effective date of registration: 20220110

Address after: 065000 Workshop 12, South District of pilot base, No. 1 Fenghua Road, economic and Technological Development Zone, Langfang City, Hebei Province

Patentee after: Zhongkeyuanjing (Hebei) Technology Co.,Ltd.

Address before: 100190 No. two, No. 1, North Haidian District, Beijing, Zhongguancun

Patentee before: Institute of Process Engineering, Chinese Academy of Sciences

TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20230607

Address after: 100190 north two street, Zhongguancun, Haidian District, Beijing, 1

Patentee after: Institute of Process Engineering, Chinese Academy of Sciences

Address before: 065000 Workshop 12, South District of pilot base, No. 1 Fenghua Road, economic and Technological Development Zone, Langfang City, Hebei Province

Patentee before: Zhongkeyuanjing (Hebei) Technology Co.,Ltd.

TR01 Transfer of patent right