CN105602187A - Automotive ABS plastic alloy material and preparation method thereof - Google Patents
Automotive ABS plastic alloy material and preparation method thereof Download PDFInfo
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- CN105602187A CN105602187A CN201610126894.8A CN201610126894A CN105602187A CN 105602187 A CN105602187 A CN 105602187A CN 201610126894 A CN201610126894 A CN 201610126894A CN 105602187 A CN105602187 A CN 105602187A
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- plastic alloy
- alloy material
- abs plastic
- automobile
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/92—Measuring, controlling or regulating
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L55/00—Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
- C08L55/02—ABS [Acrylonitrile-Butadiene-Styrene] polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92504—Controlled parameter
- B29C2948/92704—Temperature
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- 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
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention discloses an automotive ABS plastic alloy material and a preparation method thereof. ABS, SMA, EPDM, glass fiber, DCP, PP, PTT, TLCP, HDPE, alkyl methyl phosphite diplenyl ester and UHMWPE are weighed according to parts of weight, the tensile strength of the product is 60-100 MPa, the elongation at break is 140-180%, the impact strength is 35-55 kJ/m<2>, the melt flow index of the product is 6-8 g/10 min, and the rockwell hardness is 100-120; the product is high in strength, the bending strength is 100-140 MPa, the elastic modulus in bending is 2.2-2.6 GPa, the viscosity is 560-600 MPa.s, and a vicat softening point is 120-160 DEG C.
Description
Technical field
The application belongs to plastic alloy material field, relates in particular to a kind of automobile-used ABS plastic alloy material and preparation method thereof.
Background technology
Plastic alloy is to utilize the method for physical blending or chemical graft and a class new material of the high-performance that obtains, functionalization, customizations. Plastic alloy product can be widely used in the fields such as automobile, electronics, precision instrument, office equipment, packaging material, construction material. It can improve or improve the performance of existing plastics and reduce costs, and has become one of kind the most active in plastics industry, increases very rapid. China's plastic industry will be got a clear understanding of the situation, and finds gap accurately, seizes the opportunity, and strengthens input in science and technology, accelerates development Plastics Industry, the world development level of emulating.
General-purpose plastics alloy, if pvc (polyvinyl chloride), TLCP (polyethylene), EPDM (polypropylene), alkyl first diphenyl phosphite (polystyrene) are although alloy still has use value widely, but because its production technology is generally grasped, so abroad, each major company specialize in supply be mostly the engineering plastic alloy kind that added value is higher. The blend of engineering plastic alloy general reference engineering plastics (resin), mainly comprise the co-mixing system taking engineering plastics such as SMA, SMA, PA, POM (polyformaldehyde), EPDMO, PTFE (polytetrafluoroethylene (PTFE)) as main body, and DCP resin modified material.
SMA/DCP resin, Merlon and acrylonitrile-butadiene-styrene copolymer and mixture, it is the thermoplastic plastic rubber being formed by Merlon (Polycarbonate) and polyacrylonitrile (DCP) alloy, combine the excellent specific property of bi-material, the character such as the mouldability of DCP material and the mechanicalness of SMA, impact strength and heatproof, uvioresistant (UV), can be widely used on automotive interior parts, business machine, the communication apparatus, electrical home appliances and lighting apparatus.
The maximum user of world's plastic alloy product is automobile component at present, is secondly machinery and electronic devices and components. From Japanese major project plastic alloy demand structure, can find out, automotive plastic alloy accounts for 62%, and electric and business automation equipment accounts for 20%, and general precision optical machinery accounts for 6%, and medical treatment, physical culture and other account for 12%. From area, North America is maximum plastic alloy consumption area at present, accounts for 45%; Next is Europe, accounts for 34%; The Asia-pacific region accounts for 21%. In North America, EPDMO(polyphenylene oxide) alloy accounts for the more than 25% of plastic alloy total demand, wherein especially with EPDMO/PA(SMA), the having the call of EPDMO/SMA (PETG) and EPDMO/SMA (polybutylene terephthalate (PBT)) alloy; SMA (Merlon) alloy accounts for the more than 12% of aggregate demand; DCP alloy for automobile final use accounts for 99%.
China is to the research of plastic alloy since the sixties in 20th century, and development was very fast in recent years. According to statistics, at present China's plastic alloy (containing modified resin) total quantity consumed is about 1,200,000~1,400,000 tons, and 600,000 tons of domestic supply quantity not sufficients, annual import volume is up to 900,000 tons of left and right; And China's plastic alloy (being mainly blending resin and modified resin) is mainly used in household electrical appliances, electronics, automobile and other industries, compared with developed countries, the plastic alloy application market of China also has very large expanding space.
Along with China's sustained and rapid development of economy, a few years from now on China plastic alloy market demand potential is huge, and the especially rapid growth of telecommunications, automobile, building industry will pull China's engineering plastic alloy industry fast development. Expect 2008, China's five large-engineering plastics aggregate demands will reach 1,000,000 tons, and the demand of five large synthetic resin will reach 5,200 ten thousand tons, will become one of importer of global plastic alloy maximum.
ABS has good comprehensive physical and mechanical performance, fabulous low-temperature impact resistance. Dimensional stability. Electrical property, wearability, chemical proof, dyeability, finished product processing and machining are better. ABS resin is water-fast, inorganic salts, alkali and acids, is insoluble to most of alcohols and varsol, and is easily dissolved in aldehyde, ketone, ester and some chlorohydrocarbon. ABS resin heat distortion temperature is low flammable, and weatherability is poor. Melt temperature is at 217 ~ 237 DEG C, and heat decomposition temperature is more than 250 DEG C. Modified ABS material on market of today is all much adulterated regrinding-material, reworked material. Cause client's shaped article performance to differ and unstable.
At present, China plastic alloy research and produce all states in fragmentary dispersion also of two aspects, not yet forms scale, and industry integral level is low, differs greatly with Foreign Advanced Lerel. In Plastics in China alloy production breed structure, the production of the special engineering plastics alloy of high added value, almost in blank, is the production of general-purpose plastics alloy and modified product substantially. Existing 300 Duo Jia plastic alloy manufacturing enterprises of China in 2004, estimate that plastic alloy (containing modification pellet) production capacity is 700,000~800,000 tons/year, and output is 600,000 tons/year of left and right. But wherein larger enterprise only accounts for 15%, and this enterprise production of 15% accounts for the more than 70% of national plastic alloy total output. Enterprise's major part is to produce the Processing Firm of plastic alloy by plastic milling expressing technique. China's plastic alloy research and development and processing technology level have much room for improvement. And universal along with humanity concept, and the formation of novel harmonious society, designs that a kind of intensity is high, impact-resistant automobile-used ABS plastic alloy material and preparation method thereof is very important.
Summary of the invention
The technical problem solving:
The application, for above-mentioned technical problem, provides a kind of automobile-used ABS plastic alloy material and preparation method thereof, solves the technical problems such as existing plastic alloy material hot strength is low, impact strength is low, compressive strength is low.
Technical scheme:
A kind of automobile-used ABS plastic alloy material, the raw materials by weight portion proportioning of described automobile-used ABS plastic alloy material is as follows: ABS100 part; SMA1-5 part; EPDM15-35 part; Glass fibre 10-30 part; DCP25-45 part; PP1-5 part; PTT5-25 part; TLCP5-25 part; HDPE4-8 part; Alkyl first diphenyl phosphite is 4-8 part; UHMWPE1-20 part.
As a preferred technical solution of the present invention: the raw materials by weight portion proportioning of described automobile-used ABS plastic alloy material is as follows: ABS100 part; SMA2-4 part; EPDM20-30 part; Glass fibre 15-25 part; DCP30-40 part; PP2-4 part; PTT10-20 part; TLCP10-20 part; HDPE5-7 part; Alkyl first diphenyl phosphite is 5-7 part; UHMWPE5-15 part.
As a preferred technical solution of the present invention: the raw materials by weight portion proportioning of described automobile-used ABS plastic alloy material is as follows: ABS100 part; SMA2 part; EPDM20 part; 15 parts, glass fibre; DCP30 part; PP2 part; PTT10 part; TLCP10 part; HDPE5 part; Alkyl first diphenyl phosphite is 5 parts; UHMWPE5 part.
As a preferred technical solution of the present invention: the raw materials by weight portion proportioning of described automobile-used ABS plastic alloy material is as follows: ABS100 part; SMA4 part; EPDM30 part; 25 parts, glass fibre; DCP40 part; PP4 part; PTT20 part; TLCP20 part; HDPE7 part; Alkyl first diphenyl phosphite is 7 parts; UHMWPE15 part.
As a preferred technical solution of the present invention: the raw materials by weight portion proportioning of described automobile-used ABS plastic alloy material is as follows: ABS100 part; SMA3 part; EPDM25 part; 20 parts, glass fibre; DCP35 part; PP3 part; PTT15 part; TLCP15 part; HDPE6 part; Alkyl first diphenyl phosphite is 6 parts; UHMWPE10 part.
As a preferred technical solution of the present invention: the preparation method of described automobile-used ABS plastic alloy material, comprises the steps:
The first step: take ABS, SMA, EPDM, glass fibre, DCP, PP, PTT, TLCP, HDPE, alkyl first diphenyl phosphite and UHMWPE according to parts by weight proportioning;
Second step: raw material is dropped into mixer and mix, be warming up to 70-80 DEG C, mixing velocity is 80-90r/min, mixes 60-70min;
The 3rd step: mix rear input double screw extruder, barrel temperature 210-220 DEG C, 215-225 DEG C, 220-230 DEG C, 225-235 DEG C, 230-240 DEG C, extruder temperature 230-240 DEG C, head temperature 230-240 DEG C, 235-245 DEG C, 240-250 DEG C, 245-255 DEG C, 250-260 DEG C, screw speed 14-18r/min, rotating speed 30-50r/min feeds intake.
Beneficial effect:
Automobile-used ABS plastic alloy material of one of the present invention and preparation method thereof adopts above technical scheme compared with prior art, has following technique effect: 1, product hot strength 60-100MPa, elongation at break 140-180%, impact strength 35-55kJ/m2; 2, product melt flow index 6-8g/10min, Rockwell hardness 100-120; 3, product strength is high, bending strength 100-140MPa, modulus of elasticity in static bending 2.2-2.6GPa; 4, viscosity 560-600mPas, Vicat softening point 120-160 DEG C, with low cost, simple to operate, can the not division of history into periods of widespread production replace current material.
Detailed description of the invention
Embodiment 1:
Take ABS100 part according to parts by weight proportioning; SMA1 part; EPDM15 part; 10 parts, glass fibre; DCP25 part; PP1 part; PTT5 part; TLCP5 part; HDPE4 part; Alkyl first diphenyl phosphite is 4 parts; UHMWPE1 part.
Raw material is dropped into mixer and mix, be warming up to 70 DEG C, mixing velocity is 80r/min, mixes 60min.
Mix rear input double screw extruder, 210 DEG C, 215 DEG C, 220 DEG C, 225 DEG C, 230 DEG C of barrel temperatures, 230 DEG C of extruder temperatures, 230 DEG C, 235 DEG C, 240 DEG C, 245 DEG C, 250 DEG C of head temperatures, screw speed 14r/min, rotating speed 30r/min feeds intake.
Product hot strength 60MPa, elongation at break 140%, impact strength 35kJ/m2; Product melt flow index 6g/10min, Rockwell hardness 100; Product strength is high, bending strength 100MPa, modulus of elasticity in static bending 2.2GPa; Viscosity 560mPas, 120 DEG C of Vicat softening points.
Embodiment 2:
Take ABS100 part according to parts by weight proportioning; SMA5 part; EPDM35 part; 30 parts, glass fibre; DCP45 part; PP5 part; PTT25 part; TLCP25 part; HDPE8 part; Alkyl first diphenyl phosphite is 8 parts; UHMWPE20 part.
Raw material is dropped into mixer and mix, be warming up to 80 DEG C, mixing velocity is 90r/min, mixes 70min.
Mix rear input double screw extruder, 220 DEG C, 225 DEG C, 230 DEG C, 235 DEG C, 240 DEG C of barrel temperatures, 240 DEG C of extruder temperatures, 240 DEG C, 245 DEG C, 250 DEG C, 255 DEG C, 260 DEG C of head temperatures, screw speed 18r/min, rotating speed 50r/min feeds intake.
Product hot strength 70MPa, elongation at break 150%, impact strength 40kJ/m2; Product melt flow index 6g/10min, Rockwell hardness 105; Product strength is high, bending strength 110MPa, modulus of elasticity in static bending 2.3GPa; Viscosity 570mPas, 130 DEG C of Vicat softening points.
Embodiment 3:
Take ABS100 part according to parts by weight proportioning; SMA2 part; EPDM20 part; 15 parts, glass fibre; DCP30 part; PP2 part; PTT10 part; TLCP10 part; HDPE5 part; Alkyl first diphenyl phosphite is 5 parts; UHMWPE5 part.
Raw material is dropped into mixer and mix, be warming up to 70 DEG C, mixing velocity is 80r/min, mixes 60min.
Mix rear input double screw extruder, 210 DEG C, 215 DEG C, 220 DEG C, 225 DEG C, 230 DEG C of barrel temperatures, 230 DEG C of extruder temperatures, 230 DEG C, 235 DEG C, 240 DEG C, 245 DEG C, 250 DEG C of head temperatures, screw speed 14r/min, rotating speed 30r/min feeds intake.
Product hot strength 80MPa, elongation at break 160%, impact strength 45kJ/m2; Product melt flow index 7g/10min, Rockwell hardness 110; Product strength is high, bending strength 120MPa, modulus of elasticity in static bending 2.4GPa; Viscosity 580mPas, 140 DEG C of Vicat softening points.
Embodiment 4:
Take ABS100 part according to parts by weight proportioning; SMA4 part; EPDM30 part; 25 parts, glass fibre; DCP40 part; PP4 part; PTT20 part; TLCP20 part; HDPE7 part; Alkyl first diphenyl phosphite is 7 parts; UHMWPE15 part.
Raw material is dropped into mixer and mix, be warming up to 80 DEG C, mixing velocity is 90r/min, mixes 70min.
Mix rear input double screw extruder, 220 DEG C, 225 DEG C, 230 DEG C, 235 DEG C, 240 DEG C of barrel temperatures, 240 DEG C of extruder temperatures, 240 DEG C, 245 DEG C, 250 DEG C, 255 DEG C, 260 DEG C of head temperatures, screw speed 18r/min, rotating speed 50r/min feeds intake.
Product hot strength 90MPa, elongation at break 170%, impact strength 50kJ/m2; Product melt flow index 7.5g/10min, Rockwell hardness 115; Product strength is high, bending strength 130MPa, modulus of elasticity in static bending 2.5GPa; Viscosity 590mPas, 150 DEG C of Vicat softening points.
Embodiment 5:
Take ABS100 part according to parts by weight proportioning; SMA3 part; EPDM25 part; 20 parts, glass fibre; DCP35 part; PP3 part; PTT15 part; TLCP15 part; HDPE6 part; Alkyl first diphenyl phosphite is 6 parts; UHMWPE10 part.
Raw material is dropped into mixer and mix, be warming up to 75 DEG C, mixing velocity is 85r/min, mixes 65min.
Mix rear input double screw extruder, 215 DEG C, 220 DEG C, 225 DEG C, 230 DEG C, 235 DEG C of barrel temperatures, 235 DEG C of extruder temperatures, 235 DEG C, 240 DEG C, 245 DEG C, 250 DEG C, 255 DEG C of head temperatures, screw speed 16r/min, rotating speed 40r/min feeds intake.
Product hot strength 100MPa, elongation at break 180%, impact strength 55kJ/m2; Product melt flow index 8g/10min, Rockwell hardness 120; Product strength is high, bending strength 140MPa, modulus of elasticity in static bending 2.6GPa; Viscosity 600mPas, 160 DEG C of Vicat softening points.
Composition all components in above embodiment all can business be bought.
Above-described embodiment is just for content of the present invention is set forth, instead of restriction, and therefore any change in implication and the scope suitable with claims of the present invention, all should think to be included in the scope of claims.
Claims (6)
1. an automobile-used ABS plastic alloy material, is characterized in that the raw materials by weight portion proportioning of described automobile-used ABS plastic alloy material is as follows: ABS100 part; SMA1-5 part; EPDM15-35 part; Glass fibre 10-30 part; DCP25-45 part; PP1-5 part; PTT5-25 part; TLCP5-25 part; HDPE4-8 part; Alkyl first diphenyl phosphite is 4-8 part; UHMWPE1-20 part.
2. the automobile-used ABS plastic alloy material of one according to claim 1, is characterized in that described automobile-used ABS plastic alloy material raw materials by weight portion proportioning is as follows: ABS100 part; SMA2-4 part; EPDM20-30 part; Glass fibre 15-25 part; DCP30-40 part; PP2-4 part; PTT10-20 part; TLCP10-20 part; HDPE5-7 part; Alkyl first diphenyl phosphite is 5-7 part; UHMWPE5-15 part.
3. the automobile-used ABS plastic alloy material of one according to claim 1, is characterized in that the raw materials by weight portion proportioning of described automobile-used ABS plastic alloy material is as follows: ABS100 part; SMA2 part; EPDM20 part; 15 parts, glass fibre; DCP30 part; PP2 part; PTT10 part; TLCP10 part; HDPE5 part; Alkyl first diphenyl phosphite is 5 parts; UHMWPE5 part.
4. the automobile-used ABS plastic alloy material of one according to claim 1, is characterized in that the raw materials by weight portion proportioning of described automobile-used ABS plastic alloy material is as follows: ABS100 part; SMA4 part; EPDM30 part; 25 parts, glass fibre; DCP40 part; PP4 part; PTT20 part; TLCP20 part; HDPE7 part; Alkyl first diphenyl phosphite is 7 parts; UHMWPE15 part.
5. the automobile-used ABS plastic alloy material of one according to claim 1, is characterized in that: the raw materials by weight portion proportioning of described automobile-used ABS plastic alloy material is as follows: ABS100 part; SMA3 part; EPDM25 part; 20 parts, glass fibre; DCP35 part; PP3 part; PTT15 part; TLCP15 part; HDPE6 part; Alkyl first diphenyl phosphite is 6 parts; UHMWPE10 part.
6. a preparation method for automobile-used ABS plastic alloy material described in claim 1, is characterized in that, comprises the steps:
The first step: take ABS, SMA, EPDM, glass fibre, DCP, PP, PTT, TLCP, HDPE, alkyl first diphenyl phosphite and UHMWPE according to parts by weight proportioning;
Second step: raw material is dropped into mixer and mix, be warming up to 70-80 DEG C, mixing velocity is 80-90r/min, mixes 60-70min;
The 3rd step: mix rear input double screw extruder, barrel temperature 210-220 DEG C, 215-225 DEG C, 220-230 DEG C, 225-235 DEG C, 230-240 DEG C, extruder temperature 230-240 DEG C, head temperature 230-240 DEG C, 235-245 DEG C, 240-250 DEG C, 245-255 DEG C, 250-260 DEG C, screw speed 14-18r/min, rotating speed 30-50r/min feeds intake.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CN201610126894.8A CN105602187A (en) | 2016-03-07 | 2016-03-07 | Automotive ABS plastic alloy material and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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CN201610126894.8A CN105602187A (en) | 2016-03-07 | 2016-03-07 | Automotive ABS plastic alloy material and preparation method thereof |
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CN105602187A true CN105602187A (en) | 2016-05-25 |
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CN201610126894.8A Withdrawn CN105602187A (en) | 2016-03-07 | 2016-03-07 | Automotive ABS plastic alloy material and preparation method thereof |
Country Status (1)
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CN (1) | CN105602187A (en) |
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2016
- 2016-03-07 CN CN201610126894.8A patent/CN105602187A/en not_active Withdrawn
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Application publication date: 20160525 |