CN108997707A - PI fiber reinforcement PAR/ABS resin composite materials and preparation method thereof - Google Patents
PI fiber reinforcement PAR/ABS resin composite materials and preparation method thereof Download PDFInfo
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- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 title claims abstract description 50
- 239000000463 material Substances 0.000 title claims abstract description 42
- 239000000835 fiber Substances 0.000 title claims abstract description 35
- 239000000805 composite resin Substances 0.000 title claims abstract description 26
- 230000002787 reinforcement Effects 0.000 title claims abstract description 20
- 238000002360 preparation method Methods 0.000 title claims abstract description 16
- 229920001230 polyarylate Polymers 0.000 claims abstract description 39
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 18
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 12
- 239000003365 glass fiber Substances 0.000 claims abstract description 12
- 239000000314 lubricant Substances 0.000 claims abstract description 12
- 239000007822 coupling agent Substances 0.000 claims abstract description 11
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 6
- ZZMVLMVFYMGSMY-UHFFFAOYSA-N 4-n-(4-methylpentan-2-yl)-1-n-phenylbenzene-1,4-diamine Chemical compound C1=CC(NC(C)CC(C)C)=CC=C1NC1=CC=CC=C1 ZZMVLMVFYMGSMY-UHFFFAOYSA-N 0.000 claims abstract 5
- 239000000203 mixture Substances 0.000 claims description 13
- 238000002156 mixing Methods 0.000 claims description 10
- 235000021355 Stearic acid Nutrition 0.000 claims description 5
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 5
- 238000001125 extrusion Methods 0.000 claims description 5
- 238000002844 melting Methods 0.000 claims description 5
- 230000008018 melting Effects 0.000 claims description 5
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 5
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 5
- 239000008117 stearic acid Substances 0.000 claims description 5
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims description 4
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 claims description 4
- 239000000945 filler Substances 0.000 claims description 4
- 239000012948 isocyanate Substances 0.000 claims description 4
- 150000002513 isocyanates Chemical class 0.000 claims description 4
- 229940099259 vaseline Drugs 0.000 claims description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 2
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 claims 1
- VGGRCVDNFAQIKO-UHFFFAOYSA-N formic anhydride Chemical compound O=COC=O VGGRCVDNFAQIKO-UHFFFAOYSA-N 0.000 claims 1
- 239000002245 particle Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 238000007711 solidification Methods 0.000 claims 1
- 230000008023 solidification Effects 0.000 claims 1
- 239000002131 composite material Substances 0.000 abstract description 14
- 229920000642 polymer Polymers 0.000 abstract description 8
- 239000000126 substance Substances 0.000 abstract description 4
- 230000035939 shock Effects 0.000 abstract 1
- 239000011347 resin Substances 0.000 description 21
- 229920005989 resin Polymers 0.000 description 21
- 229920003023 plastic Polymers 0.000 description 9
- 239000004033 plastic Substances 0.000 description 9
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 5
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 5
- 230000003712 anti-aging effect Effects 0.000 description 5
- 238000009413 insulation Methods 0.000 description 5
- 229920006351 engineering plastic Polymers 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 239000002861 polymer material Substances 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- 239000004264 Petrolatum Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229940066842 petrolatum Drugs 0.000 description 2
- 235000019271 petrolatum Nutrition 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229920003232 aliphatic polyester Polymers 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- AOWKSNWVBZGMTJ-UHFFFAOYSA-N calcium titanate Chemical compound [Ca+2].[O-][Ti]([O-])=O AOWKSNWVBZGMTJ-UHFFFAOYSA-N 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- -1 coatings Polymers 0.000 description 1
- 229920000891 common polymer Polymers 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Chemical group CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 229920006253 high performance fiber Polymers 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- SBOJXQVPLKSXOG-UHFFFAOYSA-N o-amino-hydroxylamine Chemical group NON SBOJXQVPLKSXOG-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 238000011112 process operation Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
- C08J5/046—Reinforcing macromolecular compounds with loose or coherent fibrous material with synthetic macromolecular fibrous material
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2355/00—Characterised by the use of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08J2323/00 - C08J2353/00
- C08J2355/02—Acrylonitrile-Butadiene-Styrene [ABS] polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2467/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2479/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen, or carbon only, not provided for in groups C08J2461/00 - C08J2477/00
- C08J2479/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
- C08J2479/08—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/04—Ingredients characterised by their shape and organic or inorganic ingredients
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
- C08K2003/265—Calcium, strontium or barium carbonate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/14—Glass
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Abstract
Description
技术领域technical field
本发明属于树脂复合材料技术领域,具体涉及PI纤维增强PAR/ABS树脂复合材料及其制备方法。The invention belongs to the technical field of resin composite materials, and in particular relates to PI fiber reinforced PAR/ABS resin composite materials and a preparation method thereof.
背景技术Background technique
高分子材料是以高分子化合物为基础的材料,包括塑料、橡胶、纤维、涂料、高分子合金、高分子基复合材料以及共患难高分子材料等,高分子材料的制备与改性是材料领域中的重要发展趋势。塑料、合成纤维和合成橡胶被称为现代高分子三大合成材料,合成树脂作为塑料的主要成分其重要性不言而喻,也可直接用于加工成型广泛应用于各行各业。Polymer materials are materials based on polymer compounds, including plastics, rubber, fibers, coatings, polymer alloys, polymer-based composite materials, and common polymer materials. The preparation and modification of polymer materials is the field of materials. important trends in development. Plastic, synthetic fiber and synthetic rubber are known as the three major synthetic materials of modern polymers. The importance of synthetic resin as the main component of plastic is self-evident. It can also be directly used for processing and molding and is widely used in various industries.
ABS树脂是丙烯腈-丁二烯-苯乙烯的三元共聚物,是一种强度高、韧性好、抗冲击性好,易于加工成型的热塑型高分子材料。但它的热导率低、耐老化性差。聚芳酯(PAR)是分子主链中带有芳香环和醚键的聚酯树脂,不仅具有很好的力学性能,且与脂肪族聚酯、聚碳酸酯(PC)相比,具有更好的耐热性,阻燃性,和良好的耐候性,但它的熔融黏度高、流动性差加工性能不好。ABS resin is a terpolymer of acrylonitrile-butadiene-styrene. It is a thermoplastic polymer material with high strength, good toughness, good impact resistance and easy processing. But it has low thermal conductivity and poor aging resistance. Polyarylate (PAR) is a polyester resin with aromatic rings and ether bonds in the main chain of the molecule. It not only has good mechanical properties, but also has better mechanical properties than aliphatic polyesters and polycarbonate (PC). Excellent heat resistance, flame retardancy, and good weather resistance, but it has high melt viscosity, poor fluidity and poor processing performance.
如何制备一种具有良好机械性能、阻燃性能的多功能复合材料,是本领域。How to prepare a multifunctional composite material with good mechanical properties and flame retardancy is in the art.
发明内容Contents of the invention
本部分的目的在于概述本发明的实施例的一些方面以及简要介绍一些较佳实施例。在本部分以及本申请的说明书摘要和发明名称中可能会做些简化或省略以避免使本部分、说明书摘要和发明名称的目的模糊,而这种简化或省略不能用于限制本发明的范围。The purpose of this section is to outline some aspects of embodiments of the invention and briefly describe some preferred embodiments. Some simplifications or omissions may be made in this section, as well as in the abstract and titles of this application, to avoid obscuring the purpose of this section, the abstract and titles, and such simplifications or omissions should not be used to limit the scope of the invention.
作为本发明其中一个方面,本发明克服现有技术中存在的不足,提供一种纤维增强PAR/ABS树脂复合材料。As one aspect of the present invention, the present invention overcomes the deficiencies in the prior art and provides a fiber-reinforced PAR/ABS resin composite material.
为解决上述技术问题,本发明提供了如下技术方案:一种纤维增强PAR/ABS树脂复合材料,其包括,ABS树脂、聚芳酯、碳酸钙、固化剂、润滑剂、偶联剂、防老剂4020、PI纤维、玻璃纤维,其中,以质量份数计,所述ABS树脂含量为75~125份、所述聚芳酯含量为75~125份、所述防老剂4020含量为2~3份、所述PI纤维含量为15~55份、所述玻璃纤维含量为15~55份、所述碳酸钙含量为50~70份、所述固化剂含量为2~4份、所述润滑剂含量为3~5份、所述偶联剂含量为5~7份。In order to solve the above-mentioned technical problems, the present invention provides the following technical solutions: a fiber-reinforced PAR/ABS resin composite material, which includes ABS resin, polyarylate, calcium carbonate, curing agent, lubricant, coupling agent, anti-aging agent 4020, PI fiber, glass fiber, wherein, in parts by mass, the content of the ABS resin is 75-125 parts, the content of the polyarylate is 75-125 parts, and the content of the anti-aging agent 4020 is 2-3 parts , the content of the PI fiber is 15-55 parts, the content of the glass fiber is 15-55 parts, the content of the calcium carbonate is 50-70 parts, the content of the curing agent is 2-4 parts, the content of the lubricant 3 to 5 parts, and the content of the coupling agent is 5 to 7 parts.
作为本发明所述的纤维增强PAR/ABS树脂复合材料的一种优选方案:所述固化剂由异氰酸酯和邻苯二甲酸酐组成,其中,以质量份数计,所述异氰酸酯含量为1.5份、所述邻苯二甲酸酐含量为1.5份。As a preferred version of the fiber-reinforced PAR/ABS resin composite material of the present invention: the curing agent is composed of isocyanate and phthalic anhydride, wherein, in parts by mass, the content of the isocyanate is 1.5, The content of the phthalic anhydride is 1.5 parts.
作为本发明所述的纤维增强PAR/ABS树脂复合材料的一种优选方案:所述润滑剂由凡士林和硬脂酸组成,其中,以质量份数计,所述凡士林含量为2.5份、所述硬脂酸含量为1.5份。As a preferred version of the fiber-reinforced PAR/ABS resin composite material of the present invention: the lubricant is composed of petrolatum and stearic acid, wherein, in parts by mass, the petrolatum content is 2.5 parts, the Stearic acid content is 1.5 parts.
作为本发明所述的纤维增强PAR/ABS树脂复合材料的一种优选方案:所述偶联剂由MTMS和TEOS组成,其中,以质量份数计,所述MTMS含量为3份、所述TEOS含量为3份。As a preferred version of the fiber-reinforced PAR/ABS resin composite material of the present invention: the coupling agent is composed of MTMS and TEOS, wherein, in parts by mass, the MTMS content is 3 parts, the TEOS Servings are 3 servings.
作为本发明的另一个方面,本发明克服现有技术中存在的不足,提供所述的纤维增强PAR/ABS树脂复合材料的制备方法。As another aspect of the present invention, the present invention overcomes the deficiencies in the prior art and provides a preparation method of the fiber-reinforced PAR/ABS resin composite material.
为解决上述技术问题,本发明提供了如下技术方案:所述的纤维增强PAR/ABS树脂复合材料的制备方法,其包括,In order to solve the above-mentioned technical problems, the present invention provides the following technical scheme: the preparation method of the described fiber reinforced PAR/ABS resin composite material, which comprises,
将ABS树脂和聚芳酯进行物理混合;Physically mix ABS resin and polyarylate;
投入双螺杆挤出机,加入填料,同时加入固化剂;Put into twin-screw extruder, add filler, and add curing agent at the same time;
通过双螺杆挤出机混炼熔融挤出,冷却,干燥;Mix and melt extrude through a twin-screw extruder, cool and dry;
加入润滑剂、偶联剂、防老剂4020,混合均匀后投入双螺杆挤出机;Add lubricant, coupling agent, anti-aging agent 4020, mix well and put into twin-screw extruder;
将PI纤维预处理,制成微米级的纤维短丝,加入双螺杆挤出机,同时加入玻璃纤维;Pretreat PI fibers to make micron-sized fiber short filaments, add them to the twin-screw extruder, and add glass fibers at the same time;
混合后通过双螺杆挤出机混炼熔融挤出。After mixing, knead and melt extrude through a twin-screw extruder.
作为本发明所述的纤维增强PAR/ABS树脂复合材料的制备方法的一种优选方案:所述通过双螺杆挤出机混炼熔融挤出,冷却,干燥;其中,挤出机的螺杆速度为300~400rpm,各段温度为220℃,225℃,230℃,240℃,245℃,250℃,255℃,260℃,压力为4.5MPa。As a preferred version of the preparation method of the fiber-reinforced PAR/ABS resin composite material of the present invention: the mixing and melting extrusion of the twin-screw extruder, cooling, and drying; wherein, the screw speed of the extruder is 300~400rpm, the temperature of each stage is 220°C, 225°C, 230°C, 240°C, 245°C, 250°C, 255°C, 260°C, and the pressure is 4.5MPa.
作为本发明所述的纤维增强PAR/ABS树脂复合材料的制备方法的一种优选方案:所述混合后通过双螺杆挤出机混炼熔融挤出,其中,挤出机的螺杆速度为300~400rpm,各段温度为290℃,295℃,300℃,305℃,310℃,315℃,320℃,325℃,压力为4.5MPa。As a preferred version of the preparation method of the fiber-reinforced PAR/ABS resin composite material of the present invention: after the mixing, the twin-screw extruder is mixed and melt-extruded, wherein the screw speed of the extruder is 300- 400rpm, the temperature of each stage is 290°C, 295°C, 300°C, 305°C, 310°C, 315°C, 320°C, 325°C, and the pressure is 4.5MPa.
作为本发明所述的纤维增强PAR/ABS树脂复合材料的制备方法的一种优选方案:还包括,将双螺杆挤出机挤出的颗粒取出,冷却后,在80℃烘箱中干燥。As a preferred solution of the preparation method of the fiber-reinforced PAR/ABS resin composite material of the present invention: it also includes taking out the pellets extruded by the twin-screw extruder, cooling them, and drying them in an oven at 80°C.
本发明的有益效果:本发明以ABS树脂和PAR树脂做高分子共混改性,通过双螺杆挤出机的高温高压使两种树脂熔融混合,并挤出造粒制得PAR/ABS树脂,然后以此作为基体,以PI纤维作为主要增强体,玻璃纤维作为第二增强体,配以相关助剂,制得PI纤维增强的PAR/ABS复合材料。制得的多功能高分子复合材料具有强度高、韧性好、抗蠕变、抗冲击、耐化学药品、耐热性好、阻燃性好、绝缘性好等多种优良的性能。Beneficial effects of the present invention: the present invention uses ABS resin and PAR resin as macromolecule blending modification, melts and mixes the two resins through high temperature and high pressure of a twin-screw extruder, and extrudes and pelletizes to obtain PAR/ABS resin. Then use this as the matrix, PI fiber as the main reinforcement, glass fiber as the second reinforcement, and related additives to prepare PI fiber-reinforced PAR/ABS composite material. The prepared multifunctional polymer composite material has many excellent properties such as high strength, good toughness, creep resistance, impact resistance, chemical resistance, good heat resistance, good flame retardancy, and good insulation.
具体实施方式Detailed ways
为使本发明的上述目的、特征和优点能够更加明显易懂,下面结合具体实施例对本发明的具体实施方式做详细的说明。In order to make the above objects, features and advantages of the present invention more comprehensible, the specific implementation of the present invention will be described in detail below in conjunction with specific examples.
在下面的描述中阐述了很多具体细节以便于充分理解本发明,但是本发明还可以采用其他不同于在此描述的其它方式来实施,本领域技术人员可以在不违背本发明内涵的情况下做类似推广,因此本发明不受下面公开的具体实施例的限制。In the following description, a lot of specific details are set forth in order to fully understand the present invention, but the present invention can also be implemented in other ways different from those described here, and those skilled in the art can do it without departing from the meaning of the present invention. By analogy, the present invention is therefore not limited to the specific examples disclosed below.
其次,此处所称的“一个实施例”或“实施例”是指可包含于本发明至少一个实现方式中的特定特征、结构或特性。在本说明书中不同地方出现的“在一个实施例中”并非均指同一个实施例,也不是单独的或选择性的与其他实施例互相排斥的实施例。Second, "one embodiment" or "an embodiment" referred to herein refers to a specific feature, structure or characteristic that may be included in at least one implementation of the present invention. "In one embodiment" appearing in different places in this specification does not all refer to the same embodiment, nor is it a separate or selective embodiment that is mutually exclusive with other embodiments.
本发明PI纤维增强PAR/ABS树脂复合材料的制备方法为:The preparation method of PI fiber reinforced PAR/ABS resin composite material of the present invention is:
将ABS树脂和PAR树脂按照一定质量配比进行物理混合;Physically mix ABS resin and PAR resin according to a certain mass ratio;
将物料投入双螺杆挤出机,再加入部分填料钛酸钙、钛白粉、滑石粉的一种,同时加入固化剂异氰酸酯、乙二胺(EDA)、邻苯二甲酸酐的一种;Put the material into the twin-screw extruder, then add some fillers such as calcium titanate, titanium dioxide, and talcum powder, and at the same time add one of the curing agent isocyanate, ethylenediamine (EDA), and phthalic anhydride;
将混合树脂物料通过双螺杆挤出机混炼熔融挤出,挤出机的螺杆速度为300~400rpm,各段温度为220℃,225℃,230℃,240℃,245℃,250℃,255℃,260℃,压力4.5MPa;Mix and melt the mixed resin material through a twin-screw extruder. The screw speed of the extruder is 300-400rpm, and the temperature of each section is 220°C, 225°C, 230°C, 240°C, 245°C, 250°C, 255°C ℃, 260℃, pressure 4.5MPa;
将制得的混合树脂PAR/ABS树脂取出,冷却,干燥;The prepared mixed resin PAR/ABS resin is taken out, cooled and dried;
将PAR/ABS树脂中加入一定量的润滑剂凡士林、硬脂酸的一种,加入偶联剂KH560、HDTMS、MTMS、TEOS的一种或几种,加入防老剂4020,混合均匀后投入双螺杆挤出机;Add a certain amount of lubricant Vaseline and stearic acid to the PAR/ABS resin, add one or more coupling agents KH560, HDTMS, MTMS, TEOS, add anti-aging agent 4020, mix well and put it into the twin-screw extruder;
将PI纤维预处理,制成微米级的纤维短丝,作为主要增强体加入混合挤出机,同时加入玻璃纤维作为第二增强体;The PI fiber is pretreated to make micron-scale fiber short filaments, which are added to the mixing extruder as the main reinforcement, and glass fiber is added as the second reinforcement;
将混合的纤维、树脂等物料通过双螺杆挤出机混炼熔融挤出,挤出机的螺杆速度为300~400rpm,各段温度为290℃,295℃,300℃,305℃,310℃,315℃,320℃,325℃,压力4.5MPa;The mixed fiber, resin and other materials are mixed, melted and extruded through a twin-screw extruder. The screw speed of the extruder is 300-400rpm, and the temperature of each section is 290°C, 295°C, 300°C, 305°C, 310°C, 315°C, 320°C, 325°C, pressure 4.5MPa;
将双螺杆挤出机挤出的颗粒取出,冷却后,在80℃烘箱中干燥,即可制得PI纤维增强的PAR/ABS树脂复合材料。The granules extruded by the twin-screw extruder are taken out, cooled, and dried in an oven at 80°C to obtain a PI fiber-reinforced PAR/ABS resin composite material.
实施例1:Example 1:
选用不同树脂配比及不同助剂配比来制造本产品复合材料,样品的配方如表1所示:Different resin ratios and different additive ratios are used to manufacture the composite material of this product. The formula of the sample is shown in Table 1:
表1Table 1
本发明PI纤维增强PAR/ABS树脂复合材料的制备方法为:The preparation method of PI fiber reinforced PAR/ABS resin composite material of the present invention is:
将ABS树脂和PAR树脂按照样品的质量配比分别进行物理混合;Physically mix ABS resin and PAR resin according to the mass ratio of the sample;
将物料投入双螺杆挤出机,再分别加入样品的填料,分别加入样品的固化剂;Put the material into the twin-screw extruder, then add the filler of the sample and the curing agent of the sample respectively;
将混合树脂物料通过双螺杆挤出机混炼熔融挤出,挤出机的螺杆速度为350rpm,各段温度为220℃,225℃,230℃,240℃,245℃,250℃,255℃,260℃,压力4.5MPa;Mix and melt the mixed resin material through a twin-screw extruder, the screw speed of the extruder is 350rpm, and the temperature of each section is 220°C, 225°C, 230°C, 240°C, 245°C, 250°C, 255°C, 260°C, pressure 4.5MPa;
将制得的混合树脂PAR/ABS树脂取出,冷却,干燥;The prepared mixed resin PAR/ABS resin is taken out, cooled and dried;
将PAR/ABS树脂中分别加入样品的润滑剂,分别加入样品的偶联剂,分别加入样品的防老剂4020,混合均匀后投入双螺杆挤出机;Add the lubricant of the sample to the PAR/ABS resin, the coupling agent of the sample, and the anti-aging agent 4020 of the sample, mix well and put it into the twin-screw extruder;
将PI纤维预处理,制成微米级的纤维短丝,分别按照样品的质量份数作为主要增强体加入混合挤出机,分别加入样品质量份数的玻璃纤维作为第二增强体;The PI fiber is pretreated to make micron-scale fiber short filaments, which are added to the mixing extruder according to the mass fraction of the sample as the main reinforcement, and the glass fiber is added as the second reinforcement in the mass fraction of the sample;
将混合的纤维、树脂等物料通过双螺杆挤出机混炼熔融挤出,挤出机的螺杆速度为350rpm,各段温度为290℃,295℃,300℃,305℃,310℃,315℃,320℃,325℃,压力4.5MPa;Mix and melt the mixed fiber, resin and other materials through a twin-screw extruder, the screw speed of the extruder is 350rpm, and the temperature of each section is 290°C, 295°C, 300°C, 305°C, 310°C, 315°C , 320°C, 325°C, pressure 4.5MPa;
将双螺杆挤出机挤出的颗粒取出,冷却后,在80℃烘箱中干燥,即可分别制得样品的PI纤维增强的PAR/ABS树脂复合材料。The granules extruded by the twin-screw extruder were taken out, cooled, and dried in an oven at 80°C to prepare the PI fiber-reinforced PAR/ABS resin composite materials of the samples respectively.
实施例2:Example 2:
将制备的本发明样品制得的材料与普通树脂、工程塑料等做对比,测试其热性能负荷变形温度、维卡软化点,实验结果如表2所示:The material prepared by the sample of the present invention is compared with ordinary resins, engineering plastics, etc., and its thermal performance load deformation temperature and Vicat softening point are tested. The experimental results are as shown in Table 2:
表2Table 2
注:负荷变形温度的测定按照国家标准GB/T 1634—2004塑料-负荷变形温度的测定进行试验。Note: The determination of the deformation temperature under load is carried out in accordance with the national standard GB/T 1634-2004 Plastics - Determination of the deformation temperature under load.
微卡软化点的测定按照国家标准GB/T 1633—2000塑料维卡软化温度(VST)测定。The determination of the softening point of the microcartridge is determined according to the national standard GB/T 1633-2000 Vicat softening temperature (VST) of plastics.
实施例3:Example 3:
将制备的本发明样品制得的材料与普通树脂、工程塑料等做对比,测试其力学性能,实验结果如表3所示:The material prepared by the sample of the present invention is compared with ordinary resins, engineering plastics, etc., and its mechanical properties are tested. The experimental results are as shown in table 3:
表3table 3
冲击强度按照国家标准GB/T 1843—2008塑料悬臂梁冲击强度的测定进行。The impact strength is determined according to the national standard GB/T 1843-2008 Plastic Izod Impact Strength.
拉伸强度的测定按照国家标准GB/T 1040—2006塑料拉伸性能的测定进行。The determination of tensile strength is carried out in accordance with the national standard GB/T 1040-2006 Determination of tensile properties of plastics.
弯曲强度的测定按照国家标准GB/T 9341—2000塑料弯曲性能的测定进行。The determination of the bending strength is carried out according to the national standard GB/T 9341-2000 Determination of the bending properties of plastics.
实施例4:Example 4:
将制备的本发明样品2制得的材料与普通树脂、工程塑料等做对比,测试其绝缘性能,实验结果如表4所示:The prepared material of sample 2 of the present invention is compared with ordinary resins, engineering plastics, etc., and its insulation performance is tested. The experimental results are as shown in Table 4:
表4Table 4
介电强度的测定按照ASTM D149—97(2004)固体电绝缘材料在工业电源频率下的介电击穿电压和介电强度的试验方法进行。The measurement of dielectric strength is carried out according to ASTM D149-97 (2004) test method for dielectric breakdown voltage and dielectric strength of solid electrical insulating materials at industrial power frequency.
实施例5:Example 5:
将制备的本发明样品制得的材料与普通树脂、工程塑料等做对比,测试其绝缘阻燃性能,实验结果如表5所示:The materials prepared by the samples of the present invention were compared with ordinary resins, engineering plastics, etc., and their insulation and flame retardancy were tested. The experimental results are shown in Table 5:
表5table 5
阻燃性按照UL 94-2009设备和器具部件用塑料材料易燃性的试验。Flame Retardancy According to UL 94-2009 Test for Flammability of Plastic Materials for Equipment and Appliance Components.
本发明以ABS树脂和PAR树脂做高分子共混改性,通过双螺杆挤出机的高温高压使两种树脂熔融混合,并挤出造粒制得PAR/ABS树脂,然后以此作为基体,以PI纤维作为主要增强体,玻璃纤维作为第二增强体,配以相关助剂,制得PI纤维增强的PAR/ABS复合材料。制得的多功能高分子复合材料具有强度高、韧性好、抗蠕变、抗冲击、耐化学药品、耐热性好、阻燃性好、绝缘性好等多种优良的性能。The present invention uses ABS resin and PAR resin as polymer blending modification, melts and mixes the two resins through high temperature and high pressure of a twin-screw extruder, and extrudes and granulates to obtain PAR/ABS resin, which is then used as a matrix. Using PI fiber as the main reinforcement, glass fiber as the second reinforcement, and related additives, the PAR/ABS composite material reinforced by PI fiber was prepared. The prepared multifunctional polymer composite material has many excellent properties such as high strength, good toughness, creep resistance, impact resistance, chemical resistance, good heat resistance, good flame retardancy, and good insulation.
本发明由于ABS、PAR树脂本身就有很好的强度和力学性能,加之PI纤维做增强体加工制成的复合材料具有极高的硬度、拉伸强度、弯曲强度等优良的力学性能。且具有突出的抗蠕变性、尺寸稳定性等。In the present invention, ABS and PAR resins have good strength and mechanical properties, and the composite material processed by adding PI fibers as reinforcements has excellent mechanical properties such as extremely high hardness, tensile strength, and bending strength. And has outstanding creep resistance, dimensional stability, etc.
本发明制备的复合材料,除了两种树脂都具有的良好的力学性能外,提供了比ABS树脂更好的耐热性,同时又很好的提供了流动性、易于加工成型等优势,两种树脂协同增益,不但保持着各自的固有性能,且最大限度发挥各自材料组分的特性,并赋予单一材料所不具备的优良特殊性能。The composite material prepared by the present invention, in addition to the good mechanical properties of the two resins, provides better heat resistance than the ABS resin, and at the same time provides good fluidity and easy processing and molding. The synergistic gain of resin not only maintains their own inherent properties, but also maximizes the characteristics of their respective material components, and endows them with excellent special properties that a single material does not possess.
本发明在制备复合材料时,以高性能纤维PI纤维为增强体,使得PAR/ABS混合树脂的力学性能有进一步有所提高,且由于芳杂环的共轭效应,使其耐热性和热稳定性也大大提高,从而就使材料在高温下的力学性能保持率很高。同时由于PI分子结构中虽含有大量的极性基团,如羰基、氨基、醚基等,但因它们结构对称、玻璃化温度高、刚性大等缘故影响了极性基团的活动,从而赋予了复合材料新的阻燃性、绝缘性等优异性能。When the present invention prepares the composite material, the high-performance fiber PI fiber is used as the reinforcement, so that the mechanical properties of the PAR/ABS mixed resin are further improved, and due to the conjugation effect of the aromatic heterocycle, the heat resistance and heat resistance are improved. The stability is also greatly improved, so that the mechanical property retention rate of the material at high temperature is very high. At the same time, although the molecular structure of PI contains a large number of polar groups, such as carbonyl, amino, ether groups, etc., but because of their symmetrical structure, high glass transition temperature, and high rigidity, the activities of polar groups are affected, thus giving The new flame retardancy, insulation and other excellent properties of the composite material are achieved.
本发明所制备的复合材料,产品稳定性好、耐油、耐大多有机溶剂、耐化学药品性强。且复合材料的可塑性、可设计性强,可根据使用要求进行设计改造和加工,以满足各种特殊性能,并广泛应用与各种领域。The composite material prepared by the invention has good product stability, oil resistance, resistance to most organic solvents and strong chemical resistance. Moreover, the plasticity and designability of composite materials are strong, and they can be designed, modified and processed according to the requirements of use to meet various special properties and are widely used in various fields.
本发明制备工艺主要采用了双螺杆挤出机,其工艺操作简单,药品环保无污染,且发明物具有生物相容性,可生物降解,符合当前绿色发展的社会理念。The preparation process of the present invention mainly adopts a twin-screw extruder, the process operation is simple, the medicine is environmentally friendly and pollution-free, and the invention is biocompatible and biodegradable, which conforms to the current social concept of green development.
应说明的是,以上实施例仅用以说明本发明的技术方案而非限制,尽管参照较佳实施例对本发明进行了详细说明,本领域的普通技术人员应当理解,可以对本发明的技术方案进行修改或者等同替换,而不脱离本发明技术方案的精神和范围,其均应涵盖在本发明的权利要求范围当中。It should be noted that the above embodiments are only used to illustrate the technical solutions of the present invention without limitation, although the present invention has been described in detail with reference to the preferred embodiments, those of ordinary skill in the art should understand that the technical solutions of the present invention can be carried out Modifications or equivalent replacements without departing from the spirit and scope of the technical solution of the present invention shall be covered by the claims of the present invention.
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