CN106519635A - Surface scratch-resistant TPV composition capable of achieving secondary coating forming with ABS base material and preparation method thereof - Google Patents

Surface scratch-resistant TPV composition capable of achieving secondary coating forming with ABS base material and preparation method thereof Download PDF

Info

Publication number
CN106519635A
CN106519635A CN201610894253.7A CN201610894253A CN106519635A CN 106519635 A CN106519635 A CN 106519635A CN 201610894253 A CN201610894253 A CN 201610894253A CN 106519635 A CN106519635 A CN 106519635A
Authority
CN
China
Prior art keywords
tpv
ethylene
surface damage
damage resistant
abs
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.)
Pending
Application number
CN201610894253.7A
Other languages
Chinese (zh)
Inventor
朱旭
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.)
GUANGDONG RESEARCH INSTITUTE PETROCHEMICAL INDUSTRY
Original Assignee
GUANGDONG RESEARCH INSTITUTE PETROCHEMICAL INDUSTRY
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 GUANGDONG RESEARCH INSTITUTE PETROCHEMICAL INDUSTRY filed Critical GUANGDONG RESEARCH INSTITUTE PETROCHEMICAL INDUSTRY
Priority to CN201610894253.7A priority Critical patent/CN106519635A/en
Publication of CN106519635A publication Critical patent/CN106519635A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04Polyurethanes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/12Polypropene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/16Elastomeric ethene-propene or ethene-propene-diene copolymers, e.g. EPR and EPDM rubbers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/08Stabilised against heat, light or radiation or oxydation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • C08L2205/035Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/08Polymer mixtures characterised by other features containing additives to improve the compatibility between two polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2207/00Properties characterising the ingredient of the composition
    • C08L2207/04Thermoplastic elastomer

Abstract

The invention discloses a surface scratch-resistant TPV composition capable of achieving secondary coating forming with an ABS base material and a preparation method thereof. The TPV composition comprises the raw materials of 31%-63% of TPV, 25%-40% of thermoplastic polyester elastomer, 5%-8% of compatilizer, 2%-6% of ethylene-vinyl acetate copolymer and 5%-15% of ethylene-acrylic acid ionomer. The preparation method includes the following steps that (1) the thermoplastic polyester elastomer is dried; and (2) the thermoplastic polyester elastomer, the TPV, the compatilizer, the ethylene-vinyl acetate copolymer and the ethylene-acrylic acid ionomer are evenly mixed in proportion and then the mixture is placed into a parallel co-rotating twin-screw extruder for melt extrusion and pelleting. The surface scratch-resistant TPV composition disclosed by the invention not only has the heat resistance, ageing resistance and low compression permanent deformation of TPV materials but also has the excellent scratch resistance, and the TPV composition can achieve secondary coating with polar resin ABS. The preparation method is simple, the production process is easy to operate, and the surface scratch-resistant TPV composition can be widely used as an ABS secondary coating material with high requirements on the coating surface.

Description

A kind of and secondary Overmolded surface damage resistant TPV compositions of ABS substrate and its system Preparation Method
Technical field
The present invention relates to a kind of and secondary Overmolded surface damage resistant TPV compositions of ABS substrate and preparation method thereof, Belong to technical field of polymer materials.
Background technology
ABS resin is one of five big synthetic resin, its impact resistance, heat resistance, lower temperature resistance, chemical proofing and electricity Gas excellent performance, has the advantages that easy processing, product size are stable, surface gloss is high, easy application is coloured, can carry out table The secondary operation such as face metalling, plating, welding, hot pressing and bonding, are widely used in machinery, automobile, electronic apparatus, instrument instrument The industrial circles such as table, weaving and building, are a kind of extremely wide thermoplastics of purposes.However, being held with instrument made by ABS resin The surface of the products such as, handle hard smooth, lack body-sensing comfort level, need two to be carried out using thermoplastic elastomer (TPE) TPE to ABS It is secondary to penetrate the feel that packet splicing is covered to increase ABS products.
TPE is mainly by the blending processing such as SBC SBS or its hydride SEBS and PP, rubber softening oil Form.SBS contains double bond due to main chain, and weatherability is poor, and easily aging, SEBS is due to containing phenyl ring, resistance to ag(e)ing in strand It is poor, and SBS and SEBS wearability and scratch resistance it is all very poor.Therefore, using the TPE material with SBS or SEBS as base material ABS products obtained from secondary injection adhering are carried out to ABS, defect easily occurs in its clad surface, not only affect aesthetics and feel, and Service life is shorter.
Technology of Dynamic Vulcanized is referred to makes the vulcanization of rubber in rubber and thermoplastic molten Blending Processes, as rubber exists Also constantly mix with thermoplastic while sulfuration, therefore rubber is in thermoplastic continuous phase as dispersed phase distribution In.The thermoplastic dynamic vulcanized EPT rubber elastomer TPV prepared using Technology of Dynamic Vulcanized, sulfuration Ethylene propylene diene rubber be to be dispersed in polypropylene matrix with micron order, the elastomer not only have sulfuration EPDM The high temperature resistant of rubber, ageing-resistant, low permanent compression set, it is wear-resisting the advantages of, also with polypropylene material can with thermoplasticity processing, Recyclable the characteristics of, traditional TPE material can be replaced to be used for secondary injection adhering ABS resin in many fields.
At present, someone forms one layer of smooth surface by adding silicone damage resistant auxiliary agent in TPV in material surface, So that product brightness after being rubbed or slightly being scratched will not occur significant change, but this actually simply gives people a kind of sense Official's illusion, is not inherently eliminated the polishing scratch or cut of material surface.
The invention discloses a kind of and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, both with TPV The heat-resisting, ageing-resistant of material, low compression set, and with excellent scratch resistant performance, secondary bag can be carried out with ABS Cover, be widely used as requiring clad surface in bis- cladding material of higher ABS.
The content of the invention
It is an object of the invention to provide a kind of and secondary Overmolded surface damage resistant TPV compositions of ABS substrate.
Another object of the present invention is to provide a kind of Overmolded surface damage resistant TPV secondary with ABS substrate combine The preparation method of thing.
The technical solution used in the present invention is:
A kind of and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, which is by following weight/mass percentage composition Raw material is constituted:
TPV:31~63%;
Polyester-type thermoplastic elastomer:25~40%;
Compatilizer:5~8%;
Ethylene-vinyl acetate copolymer:2~6%;
Ethylene-propylene acids ionomer:5~15%.
Described TPV is EPT rubber dynamic vulcanization TPV.
The shore hardness of described EPT rubber dynamic vulcanization TPV is 35A~75A.
Described polyester elastomer is TPUE, at least one in thermoplastic polyester elastomer.
Described compatilizer is cyclic acid anhydride type compatilizer.
Described cyclic acid anhydride type compatilizer is at least one in EPDM-g-MAH, POE-g-MAH.
Weight/mass percentage composition >=28% of vinyl acetate in described ethylene-vinyl acetate copolymer.
Sodium salt, ethylene-acrylic acid copolymer of the described ethylene-propylene acids ionomer for ethylene-acrylic acid copolymer Zinc salt, the sodium salt of ethylene-methacrylic acid copolymer, at least one in the zinc salt of ethylene-methacrylic acid copolymer.
The above-mentioned preparation method with the secondary Overmolded surface damage resistant TPV compositions of ABS substrate, including following step Suddenly:
1) by polyester-type thermoplastic elastomer in 60~80 DEG C of dryings 4~8 hours;
2) by polyester-type thermoplastic elastomer, TPV, compatilizer, ethylene-vinyl acetate copolymer and ethylene-propylene acids Ionomer is mixed in proportion, then is placed in parallel equidirectional two-screw extruder, and melting extrusion, granulation are obtained and ABS substrate Secondary Overmolded surface damage resistant TPV compositions.
The screw slenderness ratio L/D of described double screw extruder is (40~52):1, screw speed is 200~280rpm, Extrusion temperature is 80~220 DEG C.
The present invention mechanism be:The present invention in the presence of bulking agent, by melting extrusion by the not good TPV of compatibility and Polyester-type thermoplastic elastomer is effectively connected together, so as to the TPV compositions for obtaining having good adhesion with ABS substrate. And add PUR level EVA and ethylene-propylene acids ionomer, when TPV surfaces are rubbed or slightly scratched, ethene-the third The charged particle of olefin(e) acid class ionomer can be enriched in section part, section is drawn close because of electrostatic attraction mutually, while section part EVA can carry out bonding reparation to perished surface, therefore, the secondary ABS for coating and obtaining is carried out using the TPV compositions of the present invention The surface abrasion resistance scratch resistant performance of product is significantly improved, and considerably increases surface aesthetics and the use of secondary coating ABS product Life-span.
The invention has the beneficial effects as follows:Secondary with the ABS substrate Overmolded surface damage resistant TPV compositions of the present invention Both there is the heat-resisting, ageing-resistant of TPV material, low compression set, and with excellent scratch resistant performance, can be with polarity tree Fat ABS carries out secondary cladding, and preparation method is simple, and production process is easy to operate, is widely used as higher to clad surface requirement Bis- cladding material of ABS, are such as used as electric tool ABS handles cladding crust, coffee machine ABS handles cladding crust, electric shaver ABS handles cladding crust etc..
Specific embodiment
A kind of and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, which is by following weight/mass percentage composition Raw material is constituted:
TPV:31~63%;
Polyester-type thermoplastic elastomer:25~40%;
Compatilizer:5~8%;
Ethylene-vinyl acetate copolymer:2~6%;
Ethylene-propylene acids ionomer:5~15%.
Preferably, described TPV is EPT rubber dynamic vulcanization TPV.
Preferably, the shore hardness of described EPT rubber dynamic vulcanization TPV is 35A~75A.
Preferably, described polyester elastomer is TPUE (TPU), thermoplastic polyester elastomer (TPEE) at least one in.
It is further preferred that described TPUE is the thermoplasticity that BASF AG's trade mark is C65AHPM Polyurethane elastomer, described thermoplastic polyester elastomer are the thermoplastic polyester elastomer that the LG company trade mark is 1028D.
Preferably, described compatilizer is cyclic acid anhydride type compatilizer.
Preferably, described cyclic acid anhydride type compatilizer is at least one in EPDM-g-MAH, POE-g-MAH.
It is further preferred that described cyclic acid anhydride type compatilizer is Ningbo NengZhiGuang New Materials Science Co., Ltd's trade mark For the EPDM-g-MAH of MC512, Foshan Ge Bang macromolecules Science and Technology Ltd. trade mark for GB100 POE-g-MAH at least It is a kind of.
Preferably, in described ethylene-vinyl acetate copolymer (EVA) vinyl acetate weight/mass percentage composition >=28%.
It is further preferred that it is the EVA of 40W, Taiwan that described ethylene-vinyl acetate copolymer is E.I.Du Pont Company's trade mark The modeling company trade mark is at least one in the EVA of 7760H.
Preferably, sodium salt, ethylene-acrylic acid of the described ethylene-propylene acids ionomer for ethylene-acrylic acid copolymer In the zinc salt of copolymer, the sodium salt of ethylene-methacrylic acid copolymer, the zinc salt of ethylene-methacrylic acid copolymer at least It is a kind of.
It is further preferred that described ethylene-propylene acids ionomer is the second that E.I.Du Pont Company's trade mark is Surlyn8920 The sodium salt (Na-E/MAA) of alkene-methacrylic acid copolymer.
The above-mentioned preparation method with the secondary Overmolded surface damage resistant TPV compositions of ABS substrate, including following step Suddenly:
1) by polyester-type thermoplastic elastomer in 60~80 DEG C of dryings 4~8 hours;
2) by polyester-type thermoplastic elastomer, TPV, compatilizer, ethylene-vinyl acetate copolymer and ethylene-propylene acids Ionomer is mixed in proportion, then is placed in parallel equidirectional two-screw extruder, and melting extrusion, granulation are obtained and ABS substrate Secondary Overmolded surface damage resistant TPV compositions.
Preferably, the screw slenderness ratio L/D of described double screw extruder is (40~52):1, screw speed be 200~ 280rpm, extrusion temperature are 80~220 DEG C.
The present invention is made further explanation and description with reference to specific embodiment.
Embodiment 1:
A kind of and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, the following (quality hundred of its raw material components Divide content):
TPV (self-control, shore hardness 35A):31%;
TPU (C65AHPM, BASF):40%;
EPDM-g-MAH (MC512, the light of energy):8%;
EVA (40W, Du Pont):6%;
Na-E/MAA (Surlyn8920, Du Pont):15%.
The preparation method of above-mentioned secondary with ABS substrate Overmolded surface damage resistant TPV compositions, including following step Suddenly:
1) TPU is dried process, 80 DEG C of oven temperature, 4 hours drying times in vacuum drying oven;
2) by step 1) dried TPU, TPV, EPDM-g-MAH, EVA, Na-E/MAA mix in proportion, be placed in Melting extrusion, granulation in parallel equidirectional two-screw extruder, obtain Overmolded surface damage resistant TPV secondary with ABS substrate Composition.
The screw slenderness ratio L/D of described double screw extruder is 40:1, screw speed is 280rpm, screw zones and machine Head temperature is 80,190,190,200,200,210,210,210,210,210/200 DEG C.
Embodiment 2:
A kind of and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, the following (quality hundred of its raw material components Divide content):
TPV (self-control, shore hardness 45A):40%;
TPU (C65AHPM, BASF):35%;
EPDM-g-MAH (MC512, the light of energy):6%;
EVA (40W, Du Pont):4%;
Na-E/MAA (Surlyn8920, Du Pont):15%.
The preparation method of above-mentioned secondary with ABS substrate Overmolded surface damage resistant TPV compositions, including following step Suddenly:
1) TPU is dried process, 80 DEG C of oven temperature, 4 hours drying times in vacuum drying oven;
2) by step 1) dried TPU, TPV, EPDM-g-MAH, EVA and Na-E/MAA mix in proportion, be placed in Melting extrusion, granulation in parallel equidirectional two-screw extruder, obtain Overmolded surface damage resistant TPV secondary with ABS substrate Composition.
The screw slenderness ratio L/D of described double screw extruder is 44:1, screw speed is 280rpm, screw zones and machine Head temperature is 80,190,200,210,220,220,220,210,210,210,210/200 DEG C.
Embodiment 3:
A kind of and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, the following (quality hundred of its raw material components Divide content):
TPV (self-control, shore hardness 55A):50%;
TPU (C65AHPM, BASF):32%;
EPDM-g-MAH (MC512, the light of energy):5%;
EVA (40W, Du Pont):3%;
Na-E/MAA (Surlyn8920, Du Pont):10%.
The preparation method of above-mentioned secondary with ABS substrate Overmolded surface damage resistant TPV compositions, including following step Suddenly:
1) TPU is dried process, 70 DEG C of oven temperature, 8 hours drying times in vacuum drying oven;
2) by step 1) dried TPU, TPV, EPDM-g-MAH, EVA and Na-E/MAA mix in proportion, be placed in Melting extrusion, granulation in parallel equidirectional two-screw extruder, obtain Overmolded surface damage resistant TPV secondary with ABS substrate Composition.
The screw slenderness ratio L/D of described double screw extruder is 52:1, screw speed is 200rpm, screw zones and machine Head temperature is 80,190,200,210,220,220,220,220,210,210,210,210,210/200 DEG C.
Embodiment 4:
A kind of and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, the following (quality hundred of its raw material components Divide content):
TPV (self-control, shore hardness 65A):63%;
TPU (C65AHPM, BASF):25%;
POE-g-MAH (GB100, Ge Bang):5%;
EVA (40W, Du Pont):2%;
Na-E/MAA (Surlyn8920, Du Pont):5%.
The preparation method of above-mentioned secondary with ABS substrate Overmolded surface damage resistant TPV compositions, including following step Suddenly:
1) TPU is dried process, 70 DEG C of oven temperature, 8 hours drying times in vacuum drying oven;
2) by step 1) dried TPU, TPV, POE-g-MAH, EVA and Na-E/MAA mix in proportion, be placed in Melting extrusion, granulation in parallel equidirectional two-screw extruder, obtain Overmolded surface damage resistant TPV secondary with ABS substrate Composition.
The screw slenderness ratio L/D of described double screw extruder is 52:1, screw speed is 200rpm, screw zones and machine Head temperature is 80,190,200,210,220,220,220,220,210,210,210,210,210/200 DEG C.
Embodiment 5:
A kind of and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, the following (quality hundred of its raw material components Divide content):
TPV (self-control, shore hardness 70A):40%;
TPEE (1028D, LG):35%;
POE-g-MAH (GB100, Ge Bang):6%;
EVA (7760H, platform modeling):4%;
Na-E/MAA (Surlyn8920, Du Pont):15%.
The preparation method of above-mentioned secondary with ABS substrate Overmolded surface damage resistant TPV compositions, including following step Suddenly:
1) TPEE is dried process, 80 DEG C of oven temperature, 8 hours drying times in vacuum drying oven;
2) by step 1) dried TPEE, TPV, POE-g-MAH, EVA and Na-E/MAA mix in proportion, be placed in Melting extrusion, granulation in parallel equidirectional two-screw extruder, obtain Overmolded surface damage resistant TPV secondary with ABS substrate Composition.
The screw slenderness ratio L/D of described double screw extruder is 52:1, screw speed is 200rpm, screw zones and machine Head temperature is 80,190,200,210,220,220,220,220,210,210,210,210,210/200 DEG C.
Comparative example 1:
A kind of general T PV composition, its raw material components are following (weight/mass percentage composition):
TPV (self-control, shore hardness 45A):75%;
POE-g-MAH (GB100, Ge Bang):6%;
EVA (7760H, platform modeling):4%;
Na-E/MAA (Surlyn8920, Du Pont):15%.
The preparation method of above-mentioned general T PV composition, comprises the steps:
TPV, POE-g-MAH, EVA and Na-E/MAA are mixed in proportion, parallel equidirectional two-screw extruder is placed in Middle melting extrusion, granulation, obtain TPV compositions.
The screw slenderness ratio L/D of described double screw extruder is 52:1, screw speed is 200rpm, screw zones and machine Head temperature is 80,190,200,210,220,220,220,220,210,210,210,210,210/200 DEG C.
Comparative example 2:
A kind of general T PV composition, its raw material components are following (weight/mass percentage composition):
TPV (self-control, shore hardness 55A):63%;
TPU (C65AHPM, BASF):29%;
POE-g-MAH (GB100, Ge Bang):8%.
The preparation method of above-mentioned general T PV composition, comprises the steps:
1) TPU is dried process, 80 DEG C of oven temperature, 8 hours drying times in vacuum drying oven;
2) by step 1) dried TPU, TPV and POE-g-MAH mix in proportion, and is placed in parallel equidirectional two-screw Melting extrusion, granulation in extruder, obtain TPV compositions.
The screw slenderness ratio L/D of described double screw extruder is 48:1, screw speed is 200rpm, screw zones and machine Head temperature is 80,190,200,210,220,220,220,220,210,210,210,210/200 DEG C.
Comparative example 3:
A kind of general T PV composition, its raw material components are following (weight/mass percentage composition):
TPV (self-control, shore hardness 65A):54%;
TPEE (1028D, LG):30%;
EVA (40W, Du Pont):6%;
Na-E/MAA (Surlyn8920, Du Pont):10%.
The preparation method of above-mentioned general T PV composition, comprises the steps:
1) TPU is dried process, 80 DEG C of oven temperature, 8 hours drying times in vacuum drying oven;
2) by step 1) dried TPU, TPV, EVA and Na-E/MAA mix in proportion, it be placed in parallel in the same direction double Melting extrusion, granulation in screw extruder, obtain TPV compositions.
The screw slenderness ratio L/D of described double screw extruder is 44:1, screw speed is 200rpm, screw zones and machine Head temperature is 80,190,200,210,220,220,220,220,210,210,210,210/200 DEG C.
The raw material composition of the TPV compositions in embodiment 1~5 and comparative example 1~3 is as shown in table 1, each component in table 1 Consumption is represented with mass fraction.
The raw material composition table of the TPV compositions in 1 embodiment 1~5 of table and comparative example 1~3
TPV TPU TPEE EPDM-g-MAH POE-g-MAH EVA Na-E/MAA
Embodiment 1 31 40 0 8 0 6 15
Embodiment 2 40 35 0 6 0 4 15
Embodiment 3 50 32 0 5 0 3 10
Embodiment 4 63 0 25 0 5 2 5
Embodiment 5 40 0 35 0 6 4 15
Comparative example 1 75 0 0 0 6 4 15
Comparative example 2 63 29 0 0 8 0 0
Comparative example 3 54 0 30 0 0 6 10
Test case:
The TPV compositions that embodiment 1~5 and comparative example 1~3 are prepared are fabricated to into test piece respectively, while to ABS Secondary cladding is carried out, then carries out performance test, test result is as shown in table 2.
The performance test data of the TPV compositions of 2 embodiment 1~5 of table and comparative example 1~3
From Tables 1 and 2:
1), after bis- claddings of TPV compositions prepared by embodiment 1~5 and ABS, adhesion strength is all higher than 3N/mm, and contrasts Example 1 prepare TPV compositions it is less with the adhesion strength of ABS, only 0.12N/mm, and embodiment 1~5 preparation with TPV groups The tensile strength of compound, elongation at break and scratch resistance are superior to comparative example 1 and prepare TPV compositions, are primarily due to contrast Thermoplastic polyester elastomer is not added with example 1, composition polarity is weak, with ABS poor compatibilities, cause which with ABS poor adhesions;
2) scratch resistant performance of TPV compositions prepared by embodiment 1~5 is superior to the TPV compositions of the preparation of comparative example 2, Damage resistant agent EVA and Na-E/MAA is added in being primarily due to embodiment 1~5, can significantly improve the scratch-resistant of TPV material Wound property, and EVA and Na-E/MAA in comparative example 2, is not added with, the scratch resistance of gained TPV compositions is poor;
3) tensile strength of TPV compositions prepared by embodiment 1~5, elongation at break and tearing strength are superior to contrast TPV compositions prepared by example 3, with the addition of compatilizer EPDM-g-MAH and POE-g-MAH in being primarily due to embodiment 1~5, and Bulking agent is not added with comparative example 3;
4) in embodiment 1~4, the content of TPV is different, but the stretching of TPV composition of the change of TPV contents to obtaining The impact of intensity and elongation at break is not obvious;
5) in embodiment 1~5, EVA is different with the content of Na-E/MAA, even if the two content is relatively low, the TPV combinations for obtaining The scratch resistance of thing can still reach dL value≤0.5 after 10min, and still maintain the higher adhesion strength with ABS resin, power Learn performance unaffected, excellent combination property.
Above-described embodiment is the present invention preferably embodiment, but embodiments of the present invention not by above-described embodiment Limit, other any Spirit Essences without departing from the present invention and the change, modification, replacement made under principle, combine, simplification, Equivalent substitute mode is should be, is included within protection scope of the present invention.

Claims (10)

1. a kind of and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, it is characterised in that:Which is by following quality The raw material composition of percentage composition:
TPV:31~63%;
Polyester-type thermoplastic elastomer:25~40%;
Compatilizer:5~8%;
Ethylene-vinyl acetate copolymer:2~6%;
Ethylene-propylene acids ionomer:5~15%.
2. the according to claim 1 and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, its feature exist In:Described TPV is EPT rubber dynamic vulcanization TPV.
3. the according to claim 2 and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, its feature exist In:The shore hardness of described EPT rubber dynamic vulcanization TPV is 35A~75A.
4. the according to claim 1 and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, its feature exist In:Described polyester elastomer is TPUE, at least one in thermoplastic polyester elastomer.
5. the according to claim 1 and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, its feature exist In:Described compatilizer is cyclic acid anhydride type compatilizer.
6. the according to claim 5 and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, its feature exist In:Described cyclic acid anhydride type compatilizer is at least one in EPDM-g-MAH, POE-g-MAH.
7. the according to claim 1 and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, its feature exist In:Weight/mass percentage composition >=28% of vinyl acetate in described ethylene-vinyl acetate copolymer.
8. the according to claim 1 and secondary Overmolded surface damage resistant TPV compositions of ABS substrate, its feature exist In:Sodium salt, the zinc of ethylene-acrylic acid copolymer of the described ethylene-propylene acids ionomer for ethylene-acrylic acid copolymer At least one in salt, the sodium salt of ethylene-methacrylic acid copolymer, the zinc salt of ethylene-methacrylic acid copolymer.
9. secondary with ABS substrate Overmolded surface damage resistant TPV compositions in claim 1~8 described in any one Preparation method, it is characterised in that:Comprise the following steps:
1)By polyester-type thermoplastic elastomer in 60~80 DEG C of dryings 4~8 hours;
2)By polyester-type thermoplastic elastomer, TPV, compatilizer, ethylene-vinyl acetate copolymer and ethylene-propylene acids from poly- Thing is mixed in proportion, then is placed in parallel equidirectional two-screw extruder, melting extrusion, granulation, obtains secondary with ABS substrate Overmolded surface damage resistant TPV compositions.
10. preparation method according to claim 9, it is characterised in that:The screw slenderness ratio of described double screw extruder L/D is(40~52):1, screw speed is 200~280rpm, and extrusion temperature is 80~220 DEG C.
CN201610894253.7A 2016-10-13 2016-10-13 Surface scratch-resistant TPV composition capable of achieving secondary coating forming with ABS base material and preparation method thereof Pending CN106519635A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610894253.7A CN106519635A (en) 2016-10-13 2016-10-13 Surface scratch-resistant TPV composition capable of achieving secondary coating forming with ABS base material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610894253.7A CN106519635A (en) 2016-10-13 2016-10-13 Surface scratch-resistant TPV composition capable of achieving secondary coating forming with ABS base material and preparation method thereof

Publications (1)

Publication Number Publication Date
CN106519635A true CN106519635A (en) 2017-03-22

Family

ID=58331640

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610894253.7A Pending CN106519635A (en) 2016-10-13 2016-10-13 Surface scratch-resistant TPV composition capable of achieving secondary coating forming with ABS base material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN106519635A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106939100A (en) * 2017-04-20 2017-07-11 贵州省材料产业技术研究院 A kind of fire-retardant TPV composites of dynamic vulcanization and preparation method thereof
CN112480589A (en) * 2020-12-09 2021-03-12 上海锦湖日丽塑料有限公司 Soft-touch HIPS composition and preparation method thereof
CN114410017A (en) * 2021-12-31 2022-04-29 广东太力科技集团股份有限公司 TPV material and preparation method and application thereof
CN114410017B (en) * 2021-12-31 2024-04-26 广东太力科技集团股份有限公司 TPV material and preparation method and application thereof

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100240981B1 (en) * 1997-09-13 2000-02-01 이영일 Resin compositions having improved scratch resistance and impact strength
CN1916055A (en) * 2006-09-12 2007-02-21 北京化工大学 Method for raising fluidity of thermoplastic cross-linked rubber
CN101033325A (en) * 2006-03-08 2007-09-12 广东榕泰实业股份有限公司 Thermoplastic elastomer compositions and preparation method thereof
CN102051018A (en) * 2010-11-30 2011-05-11 深圳市盛嘉伦橡塑工业有限公司 Thermoplastic elastomer for being subjected to secondary injection adhesion with PBT (polybutylene terephthalate) material and composite molding product using same
CN103497429A (en) * 2013-09-26 2014-01-08 金发科技股份有限公司 Low-smell TPV (thermoplastic vulcanizate) formed by secondary coating with ABS (acrylonitrile-butadiene-styrene) substrate and preparation method thereof
EP2746351A1 (en) * 2012-12-20 2014-06-25 Tarkett GDL S.A. PVC-free surface covering
WO2016089647A1 (en) * 2014-12-02 2016-06-09 Dow Global Technologies Llc Dynamic vulcanization of a blend composition, methods of manufacture thereof and articles comprising the same

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100240981B1 (en) * 1997-09-13 2000-02-01 이영일 Resin compositions having improved scratch resistance and impact strength
CN101033325A (en) * 2006-03-08 2007-09-12 广东榕泰实业股份有限公司 Thermoplastic elastomer compositions and preparation method thereof
CN1916055A (en) * 2006-09-12 2007-02-21 北京化工大学 Method for raising fluidity of thermoplastic cross-linked rubber
CN102051018A (en) * 2010-11-30 2011-05-11 深圳市盛嘉伦橡塑工业有限公司 Thermoplastic elastomer for being subjected to secondary injection adhesion with PBT (polybutylene terephthalate) material and composite molding product using same
EP2746351A1 (en) * 2012-12-20 2014-06-25 Tarkett GDL S.A. PVC-free surface covering
CN103497429A (en) * 2013-09-26 2014-01-08 金发科技股份有限公司 Low-smell TPV (thermoplastic vulcanizate) formed by secondary coating with ABS (acrylonitrile-butadiene-styrene) substrate and preparation method thereof
WO2016089647A1 (en) * 2014-12-02 2016-06-09 Dow Global Technologies Llc Dynamic vulcanization of a blend composition, methods of manufacture thereof and articles comprising the same

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106939100A (en) * 2017-04-20 2017-07-11 贵州省材料产业技术研究院 A kind of fire-retardant TPV composites of dynamic vulcanization and preparation method thereof
CN112480589A (en) * 2020-12-09 2021-03-12 上海锦湖日丽塑料有限公司 Soft-touch HIPS composition and preparation method thereof
CN112480589B (en) * 2020-12-09 2022-07-19 上海锦湖日丽塑料有限公司 Soft-touch HIPS composition and preparation method thereof
CN114410017A (en) * 2021-12-31 2022-04-29 广东太力科技集团股份有限公司 TPV material and preparation method and application thereof
CN114410017B (en) * 2021-12-31 2024-04-26 广东太力科技集团股份有限公司 TPV material and preparation method and application thereof

Similar Documents

Publication Publication Date Title
CN103665540B (en) A kind of delustring PP composite material and preparation method thereof
CN102051018B (en) Thermoplastic elastomer for being subjected to secondary injection adhesion with PBT (polybutylene terephthalate) material and composite molding product using same
CN111154427B (en) Aluminum ceiling glue film structure and aluminum ceiling structure thereof
CN102807703B (en) Low gloss polypropylene composition and preparation method thereof
CN102585365B (en) Coating-free polypropylene composition with paint brightness and metal texture and preparation method thereof
CN111117524B (en) Adhesive resin for aluminum ceiling
CN108456416A (en) A kind of composition for thermoplastic elastomer and preparation method thereof for the encapsulated nylon of low temperature
CN101255262A (en) Thermoplastic elastomer capable of coating and bonding with nylon
CN102803356B (en) Composition for stretchable film
CN106084493A (en) A kind of metal-like for automobile exterior trimming parts exempts from spray coating polypropylene composite and preparation method thereof
CN107722466A (en) A kind of high-polarity polypropylene composite and preparation method thereof and the application in automobile exterior material
CN110172240A (en) Damping encapsulated ABS thermoplastic elastomer (TPE) and its manufacturing method
CN102372894A (en) Anti-static thermoplastic elastomer composite and preparation method thereof
WO2020000588A1 (en) Thermoplastic elastomer material
CN102585366A (en) Polypropylene composition with copper-colored metal texture, and preparation method and application thereof
CN103571125A (en) Elastomer nylon coating material as well as preparation method thereof
CN105882094A (en) Solar panel high-temperature-resistant anti-ultraviolet self-adhesive film
CN106519635A (en) Surface scratch-resistant TPV composition capable of achieving secondary coating forming with ABS base material and preparation method thereof
CN106947139A (en) A kind of antistatic film and preparation method thereof
CN111253717B (en) Thermoplastic elastomer and preparation method thereof
CN109627768A (en) A kind of thermoplastic dynamic vulcanized silicon rubber of high-flexibility and preparation method thereof
CN103073786B (en) A kind of polypropylene matting agent master batch and its preparation method and application
CN102832002A (en) Environment-friendly halogen-free rare-earth composite magnetic material
CN102464853B (en) Novel material for needled carpet of car
CN103665570B (en) A kind of ultralow-temperature flexibility polypropene composition and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20170322