CN105440911A - Low temperature crosslinked high molecular composite material used for MDF sheet material, and preparation method thereof - Google Patents
Low temperature crosslinked high molecular composite material used for MDF sheet material, and preparation method thereof Download PDFInfo
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- 239000002131 composite material Substances 0.000 title claims abstract description 31
- 239000000463 material Substances 0.000 title claims abstract description 11
- 238000002360 preparation method Methods 0.000 title claims abstract description 8
- 229920000642 polymer Polymers 0.000 claims abstract description 22
- 229920001225 polyester resin Polymers 0.000 claims abstract description 15
- 239000004645 polyester resin Substances 0.000 claims abstract description 15
- 238000000576 coating method Methods 0.000 claims abstract description 13
- 239000003822 epoxy resin Substances 0.000 claims abstract description 12
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 12
- 239000000049 pigment Substances 0.000 claims abstract description 7
- 239000000945 filler Substances 0.000 claims abstract description 6
- 238000002156 mixing Methods 0.000 claims abstract description 6
- 239000012752 auxiliary agent Substances 0.000 claims abstract description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 16
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical group O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 9
- 239000011248 coating agent Substances 0.000 claims description 9
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 9
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 8
- 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 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- 239000000843 powder Substances 0.000 claims description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
- 239000002270 dispersing agent Substances 0.000 claims description 4
- -1 lithopone Substances 0.000 claims description 4
- 239000004408 titanium dioxide Substances 0.000 claims description 4
- 239000004593 Epoxy Substances 0.000 claims description 3
- 238000007872 degassing Methods 0.000 claims description 3
- 229910001504 inorganic chloride Inorganic materials 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 3
- 238000007873 sieving Methods 0.000 claims description 3
- 150000005846 sugar alcohols Polymers 0.000 claims description 3
- 239000005995 Aluminium silicate Substances 0.000 claims description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 2
- 235000012211 aluminium silicate Nutrition 0.000 claims description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- 239000006229 carbon black Substances 0.000 claims description 2
- 238000001816 cooling Methods 0.000 claims description 2
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 claims description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 2
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 claims description 2
- 229940107698 malachite green Drugs 0.000 claims description 2
- 238000002844 melting Methods 0.000 claims description 2
- 230000008018 melting Effects 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- 239000004576 sand Substances 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 239000004841 bisphenol A epoxy resin Substances 0.000 claims 1
- 229920002521 macromolecule Polymers 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 9
- 238000003860 storage Methods 0.000 abstract description 9
- 239000003973 paint Substances 0.000 abstract description 5
- 238000001879 gelation Methods 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract description 2
- 230000000052 comparative effect Effects 0.000 description 9
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 244000028419 Styrax benzoin Species 0.000 description 3
- 235000000126 Styrax benzoin Nutrition 0.000 description 3
- 235000008411 Sumatra benzointree Nutrition 0.000 description 3
- 229960002130 benzoin Drugs 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 235000019382 gum benzoic Nutrition 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- PQAMFDRRWURCFQ-UHFFFAOYSA-N 2-ethyl-1h-imidazole Chemical compound CCC1=NC=CN1 PQAMFDRRWURCFQ-UHFFFAOYSA-N 0.000 description 1
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 1
- BKCCAYLNRIRKDJ-UHFFFAOYSA-N 2-phenyl-4,5-dihydro-1h-imidazole Chemical compound N1CCN=C1C1=CC=CC=C1 BKCCAYLNRIRKDJ-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000007590 electrostatic spraying Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- OSUMTOORAWCHGK-UHFFFAOYSA-N n-phenyl-1h-imidazole-2-carboxamide Chemical compound N=1C=CNC=1C(=O)NC1=CC=CC=C1 OSUMTOORAWCHGK-UHFFFAOYSA-N 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000004383 yellowing Methods 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
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
-
- 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
- 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
-
- 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
-
- 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
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
本发明涉及化工涂料领域,具体涉及一种涂覆于MDF板材外表面、对MDF板材进行保护和装饰的高分子复合材料及制备方法。复合材料中各组分及质量百分含量为,聚酯树脂30~33%、环氧树脂30~33%、颜料和填料30~37%、助剂1.6~3.5%,固化促进剂0.8~1.2%,按质量百分比,将各组分混合后通过挤出机熔融挤出混合,将挤出混合物料冷却、破碎、过筛得到产品。本发明制备高分子复合涂料,贮存稳定性优异,在38℃条件下贮存2个月后,产品的胶化时间基本无变化;固化条件为130℃/15min,固化温度低、生产效率高。The invention relates to the field of chemical coatings, in particular to a polymer composite material coated on the outer surface of an MDF board to protect and decorate the MDF board and a preparation method thereof. The components and mass percentages in the composite material are: 30-33% of polyester resin, 30-33% of epoxy resin, 30-37% of pigment and filler, 1.6-3.5% of auxiliary agent, 0.8-1.2% of curing accelerator %, according to mass percentage, after mixing the components, they are melted and extruded through an extruder to mix, and the extruded mixed material is cooled, crushed and sieved to obtain the product. The polymer composite paint prepared by the invention has excellent storage stability, and after storage at 38°C for 2 months, the gelation time of the product basically does not change; the curing condition is 130°C/15min, the curing temperature is low, and the production efficiency is high.
Description
技术领域technical field
本发明涉及化工涂料领域,具体涉及一种涂覆于MDF板材外表面、对MDF板材进行保护和装饰的高分子复合材料及制备方法。The invention relates to the field of chemical coatings, in particular to a polymer composite material coated on the outer surface of an MDF board to protect and decorate the MDF board and a preparation method thereof.
背景技术Background technique
目前MDF板材表面的处理工序综合起来分为:表面机械加工、贴面装饰、涂饰三步。其中涂饰一般采用油漆或紫外光固化涂料,在喷涂油漆的工序为:批腻子→打磨→喷漆(表面有缺陷再重复整套工序),工序周期至少4天,劳动效率低,产生VOC排放,污染环境,影响工人健康。而紫外光固化涂料只适合平面施工,对于各种形状和边缘部位光线无法照射的部位无法固化,因此应用受限制。现在市场上也有部分低温粉末涂料在MDF板材上进行应用,但基于固化促进剂的原因,该类产品的烘烤过程中,易黄变,不适合生产浅色产品,而且贮存稳定性差,在30℃条件下贮存2个月,产品的胶化时间就会明显缩短,影响了产品的正常使用。At present, the surface treatment process of MDF boards can be divided into three steps: surface machining, veneer decoration, and painting. Among them, paint or UV-curable paint is generally used for finishing. The process of spraying paint is: batch putty→grinding→painting (repeat the whole process if the surface is defective), the process cycle is at least 4 days, the labor efficiency is low, VOC emissions are generated, and the environment is polluted. , affecting the health of workers. However, UV-curable coatings are only suitable for plane construction, and cannot be cured for various shapes and edges that cannot be irradiated by light, so the application is limited. There are also some low-temperature powder coatings on the market that are used on MDF boards, but due to the curing accelerator, this type of product is easy to yellow during the baking process, and is not suitable for the production of light-colored products, and its storage stability is poor. Stored at ℃ for 2 months, the gel time of the product will be significantly shortened, which affects the normal use of the product.
发明内容Contents of the invention
为解决上述技术问题,本发明提供了一种用于涂覆在MDF板材表面的高分子复合材料,该高分子复合材料的成膜温度低,即130℃/15min固化,施工过程中无VOC排放,属于环境友好型产品,产品产用流水线施工,烘烤固化后,产品冷却至常温就可以进行下一道组装工序,劳动生产效率快,可制成各种颜色和纹理。In order to solve the above technical problems, the present invention provides a polymer composite material for coating on the surface of MDF boards. The polymer composite material has a low film forming temperature, that is, 130°C/15min curing, and there is no VOC emission during the construction process. , is an environmentally friendly product, the product is produced with assembly line construction, after baking and solidification, the product can be cooled to room temperature before the next assembly process, labor production efficiency is fast, and can be made into various colors and textures.
本发明的高分子复合材料中各组分及质量百分含量为:聚酯树脂30~33%、环氧树脂30~33%、颜料和填料30~37%、助剂1.6~3.5%,固化促进剂0.8~1.2%,In the polymer composite material of the present invention, each component and its mass percentage are: 30-33% of polyester resin, 30-33% of epoxy resin, 30-37% of pigment and filler, 1.6-3.5% of auxiliary agent, curing Accelerator 0.8~1.2%,
其中,聚酯树脂为多元醇和多元羧酸聚合而成的端羧基聚酯树脂,其酸值为65~75mgKOH/g,Tg为52~56℃,Among them, the polyester resin is a carboxyl-terminated polyester resin polymerized from polyhydric alcohol and polycarboxylic acid, its acid value is 65-75mgKOH/g, and its Tg is 52-56°C.
环氧树脂为固化剂,该环氧树脂为环氧氯丙烷和双酚A通过两步法聚合而成的双酚A型环氧树脂,其环氧当量为780~850g/eq,软化点为92~102℃,有机氯离子含量≤0.5%,无机氯离子含量≤300ppm,Epoxy resin is the curing agent. The epoxy resin is a bisphenol A type epoxy resin formed by polymerization of epichlorohydrin and bisphenol A through a two-step method. Its epoxy equivalent is 780-850g/eq, and its softening point is 92~102℃, organic chloride ion content≤0.5%, inorganic chloride ion content≤300ppm,
填料平均粒径≤10μm,具体为硫酸钡、高岭土或碳酸钙其中一种或多种,颜料为钛白粉、立德粉、炭黑、大红粉、酞箐蓝、孔雀绿或偶淡黄,The average particle size of the filler is ≤10 μm, specifically one or more of barium sulfate, kaolin or calcium carbonate, and the pigment is titanium dioxide, lithopone, carbon black, red powder, phthalocyanine blue, malachite green or even light yellow,
助剂包括流平剂、分散剂、脱气剂、松散剂、砂纹剂,其中,流平剂包括丙烯酸酯共聚物,分散剂包括甲基丙烯酸和苯乙烯的共聚物,脱气剂包括安息香或酰胺蜡,松散剂包括气相二氧化硅或氧化铝C,砂纹剂包括聚四氟乙烯蜡粉,Auxiliaries include leveling agent, dispersant, degassing agent, loosening agent, sand texture agent, wherein, leveling agent includes acrylate copolymer, dispersant includes copolymer of methacrylic acid and styrene, and degassing agent includes benzoin or amide wax, the loosening agent includes fumed silica or alumina C, the sanding agent includes polytetrafluoroethylene wax powder,
固化促进剂为2MA-OK或苯氨基甲酰基咪唑(结构式如下),利用这两种固化促进剂产品自身结构特点,提高了高分子复合材料在固化前的贮存稳定性能,使其在80℃以下基本无反应,但是却有效地降低了复合材料成膜时的固化温度,The curing accelerator is 2MA-OK or phenylcarbamoyl imidazole (structural formula is as follows). Using the structural characteristics of these two curing accelerator products, the storage stability of the polymer composite material before curing is improved, so that it can be stored below 80 ° C. There is basically no reaction, but it effectively reduces the curing temperature when the composite material is formed into a film,
(X为H)。(X is H).
本发明还提供了一种上述用于涂覆在MDF板材表面的高分子复合材料的制备方法:按质量百分比,将各组分投入混料釜进行混合,将混合好的物料通过挤出机进行熔融挤出混合,将挤出混合物料进行冷却,用破碎机将物料进行破碎,再用空气分级磨进行细粉碎和分级,最后用旋转筛分级过筛得到产品。The present invention also provides a method for preparing the above-mentioned polymer composite material for coating on the surface of MDF boards: according to the mass percentage, put each component into a mixing tank for mixing, and pass the mixed material through an extruder Melting extrusion mixing, cooling the extruded mixed material, crushing the material with a crusher, finely pulverizing and grading with an air classifying mill, and finally grading and sieving with a rotary sieve to obtain the product.
本发明的有益效果在于:本发明制备高分子复合涂料,在80℃以下基本无化学反应,贮存稳定性优异,在38℃条件下贮存2个月后,产品的胶化时间基本无变化;产品采用高压静电喷涂在经过机械加工或贴面装饰的MDF板材上,通过红外线和热风循环的加热方式固化,固化条件为130℃/15min,固化温度低、生产效率高,在固化过程中不易产生黄变,无VOC排放(同时通过130℃烘烤可去除MDF板材中的甲醛含量),固化后的板材可直接进行下道工序安装,节约时间。The beneficial effect of the present invention is that: the polymer composite paint prepared by the present invention basically has no chemical reaction below 80°C, and has excellent storage stability. After being stored at 38°C for 2 months, the gelation time of the product basically does not change; the product It adopts high-voltage electrostatic spraying on the MDF board that has been machined or veneered, and is cured by infrared rays and hot air circulation. The curing condition is 130°C/15min. The curing temperature is low and the production efficiency is high. It is not easy to produce yellow during the curing process. change, no VOC emissions (at the same time, the formaldehyde content in the MDF board can be removed by baking at 130 ° C), and the cured board can be directly installed in the next process, saving time.
本发明采用端羧基聚酯树脂和双酚A型环氧树脂,在固化促进剂2MA-OK或苯氨基甲酰基咪唑的作用下,环氧基团与聚酯树脂的羧基进行反应,交联成膜,交联后的高分子复合物耐冲击强度可达50kg/cm,柔韧性1mm,附着力0级,有机复合物的物理机械性能和耐老化性能优异,制备工艺简单,可显著提高劳动生产效率,适合工业化生产。The present invention adopts carboxyl-terminated polyester resin and bisphenol A type epoxy resin, and under the action of curing accelerator 2MA-OK or anilcarbamoyl imidazole, the epoxy group reacts with the carboxyl group of the polyester resin, and cross-links to form Membrane, cross-linked polymer composite impact strength can reach 50kg/cm, flexibility 1mm, adhesion 0 grade, organic composite has excellent physical and mechanical properties and aging resistance, simple preparation process, can significantly improve labor production Efficiency, suitable for industrial production.
附图说明Description of drawings
图1为本发明中高分子复合材料的制备方法工艺流程图。Fig. 1 is the process flow diagram of the preparation method of the polymer composite material in the present invention.
具体实施方式detailed description
以下各实施例中聚酯树脂均为多元醇和多元羧酸聚合而成的端羧基聚酯树脂,聚酯树脂的其酸值为65~75mgKOH/g,Tg为52~56℃;所用固化剂为环氧树脂,环氧当量为780~850g/eq,软化点为92~102℃,有机氯离子含量≤0.5%,无机氯离子含量≤300ppm;颜料为耐热性达到180℃以上,各种不含重金属的着色颜料或金红石型钛白粉。In each of the following examples, the polyester resins are carboxyl-terminated polyester resins formed by the polymerization of polyhydric alcohols and polycarboxylic acids. The acid value of the polyester resins is 65 to 75 mgKOH/g, and the Tg is 52 to 56° C.; the curing agent used is Epoxy resin, the epoxy equivalent is 780-850g/eq, the softening point is 92-102°C, the content of organic chloride ions is ≤0.5%, and the content of inorganic chloride ions is ≤300ppm; Coloring pigments containing heavy metals or rutile titanium dioxide.
实施例1Example 1
一种用于涂覆在MDF板材表面的高分子复合材料,具有如下配方(各组分为质量份数):聚酯树脂(HH-2562)33份、E-12环氧树脂(GES904)33份、NR950钛白23份、硫酸钡7.6份、2MA-OK1.2份、流平剂1.2份、分散剂0.7份、安息香脱气剂0.3份。A polymer composite material for coating on the surface of MDF boards, which has the following formula (the components are parts by mass): 33 parts of polyester resin (HH-2562), 33 parts of E-12 epoxy resin (GES904) 23 parts of NR950 titanium dioxide, 7.6 parts of barium sulfate, 1.2 parts of 2MA-OK, 1.2 parts of leveling agent, 0.7 parts of dispersant, and 0.3 parts of benzoin degasser.
实施例2Example 2
一种用于涂覆在MDF板材表面的高分子复合材料,具有如下配方(各组分为质量份数):聚酯树脂(HH-2562)30份、E-12环氧树脂(GES904)30份、NR950钛白23份、硫酸钡14份、苯氨基甲酰基咪唑1.2份、砂纹剂0.2份、聚乙烯蜡粉1.3、安息香脱气剂0.3份。A polymer composite material for coating on the surface of MDF boards, with the following formula (the components are parts by mass): 30 parts of polyester resin (HH-2562), 30 parts of E-12 epoxy resin (GES904) 23 parts of NR950 titanium dioxide, 14 parts of barium sulfate, 1.2 parts of anilbamoyl imidazole, 0.2 parts of sanding agent, 1.3 parts of polyethylene wax powder, and 0.3 parts of benzoin degasser.
对比实施例1Comparative Example 1
将实施例1中固化促进剂替换为2-甲基咪唑或2-乙基咪唑,其它组份及含量不变(对比实施例1与原实施例1内容大致相同,仅将其中固化促进剂品种作了改变,以说明固化促进剂对产品生产和贮存稳定性的影响)。In embodiment 1, the curing accelerator is replaced by 2-methylimidazole or 2-ethylimidazole, and other components and contents remain unchanged (the content of comparative example 1 is roughly the same as that of the original embodiment 1, only the curing accelerator species is wherein Changes were made to account for the effect of curing accelerators on product manufacturing and storage stability).
对比实施例2Comparative Example 2
将实施例2中固化促进剂替换为2-苯基咪唑啉,其它组份及含量不变(对比实施例2与原实施例2内容大致相同,仅将其中固化促进剂品种作了改变,以说明固化促进剂对产品生产和贮存稳定性的影响)。In embodiment 2, curing accelerator is replaced by 2-phenylimidazoline, and other components and content are constant (comparative example 2 is roughly the same as former embodiment 2 content, only wherein curing accelerator kind has been changed, with Describe the effect of curing accelerators on product production and storage stability).
上述各实施例、对比实施例中的用于涂覆在MDF板材表面的高分子复合材料制备方法如下:The polymer composite material preparation method that is used to be coated on the surface of MDF sheet material in above-mentioned each embodiment, comparative example is as follows:
按重量份数,将各组分投入混料釜进行混合5min,将混合好的物料通过挤出机进行熔融挤出(118℃~122℃)混合,将挤出混合物料进行冷却,用破碎机将物料破碎到厚2.5mm以下、长和宽20mm以下,再用空气分级磨进行细粉碎和分级,最后用旋转筛分级过筛得到产品,筛网目数为180目。各实施例、对比实施例所得产品的固化工艺以及各性能数据如下表:According to the number of parts by weight, put each component into the mixing tank and mix for 5 minutes, melt and extrude the mixed material through an extruder (118 ° C ~ 122 ° C) and mix, cool the extruded mixed material, and use a crusher The material is crushed to less than 2.5mm in thickness and less than 20mm in length and width, then finely crushed and classified by an air classifying mill, and finally classified and sieved by a rotary sieve to obtain the product with a mesh number of 180 mesh. The curing process and each performance data of each embodiment, comparative example gained product are as follows:
经过对比上表中数据可知,虽然对比实施例1和对比实施例2中仅将固化促进剂的品种做了改变,但是对最终性能方面影响很大,如生产难易程度(这里指的是挤出操作的难易程度:本发明需要在120℃左右条件下熔融挤出,对比实施例1、2中由于复合材料的活性太强,在挤出过程中容易发生反应,导致部分涂料提前固化形成废品,影响正常生产,造成浪费;而实施例1、2中不存在这一现象。)、耐黄变性、贮存稳定性、长时间贮存后的外观等都有较大的影响。可见,在本申请配方条件下,选取合适固化促进剂对性能有了很大的提高;此外,砂纹剂的添加可改变产品的外观,使产品具有磨砂效果。Through comparing the data in the above table, it can be seen that although only the kind of curing accelerator has been changed in comparative example 1 and comparative example 2, it has a great influence on the final performance, such as the ease of production (referring to extrusion here). Difficulty of operation: the present invention needs to be melt-extruded at about 120°C. In Comparative Examples 1 and 2, due to the high activity of the composite material, it is easy to react during the extrusion process, resulting in part of the coating being solidified in advance to form Waste product, affects normal production, causes waste; And this phenomenon does not exist in embodiment 1,2.), anti-yellowing property, storage stability, the outward appearance etc. after long-time storage all have bigger influence. It can be seen that under the formulation conditions of this application, selecting a suitable curing accelerator can greatly improve the performance; in addition, the addition of sanding agent can change the appearance of the product and make the product have a frosting effect.
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CN107652860A (en) * | 2017-10-31 | 2018-02-02 | 山东瑞丰高分子材料股份有限公司 | Medium-density plate cured powder paint and preparation method thereof |
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