CN109957253A - A kind of thermoplastic elastic material and preparation method thereof for coating glass fiber enhanced nylon - Google Patents
A kind of thermoplastic elastic material and preparation method thereof for coating glass fiber enhanced nylon Download PDFInfo
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- CN109957253A CN109957253A CN201711417157.4A CN201711417157A CN109957253A CN 109957253 A CN109957253 A CN 109957253A CN 201711417157 A CN201711417157 A CN 201711417157A CN 109957253 A CN109957253 A CN 109957253A
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
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- C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
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- 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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- 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
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
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- 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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Abstract
A kind of thermoplastic elastic material for coating glass fiber enhanced nylon of the present invention, each component including following mass fraction: 8~10 parts of styrene block copolymers, 20~30 parts of filling oil, 20~25 parts of mineral filler, 15~25 parts of compatilizer, 8.3~23.3 parts of polar resin, 5~10 parts of nylon, 0~5 part of polar lubricant, 0~0.5 part of processing aid and 0.2 part of anti-aging agent.The present invention is by being adjusted the specific selection of styrene block copolymers and proportion, being modified to mineral material, adjust the compatibility of each component, resulting thermoplastic elastic material, it is strong to coat glass fiber enhanced nylon bonding force, high melt index, good fluidity have preferable processing performance, when removing recycling, substrate surface is remained without flexible glue, can be widely applied to all kinds of handle for tool cladding of glass fiber enhanced nylon substrate.
Description
Technical field
It is specially a kind of for coating the thermoplastic elastomehc of glass fiber enhanced nylon the invention belongs to technical field of polymer materials
Elastomer material and preparation method thereof.
Background technique
Nylon is a kind of widely used engineering plastics, has many advantages, such as high mechanical strength, and heat resistance, rub resistance are good.
In recent years, nylon is widely used in toy, daily necessities, industrial products etc., product surface made of nylon material it is often harder and
Smooth, feel is poor in use, and is easy to slide.To solve this problem, upper one layer can be coated on nylon surface
Flexible glue makes it have good feel, increases the comfort of user, can also largely improve the aesthetics of product.
The products such as electric tool and pneumatic tool can generate biggish vibration in use, the thermoplasticity coated on nylon handle
Elastomer can play the role of damping, play preferable protective effect.
Common thermoplastic elastomer (TPE) (TPE) encapsulated products mainly have the encapsulated polypropylene of TPE (PP), TPE encapsulated in the market
Acrylonitrile-butadiene-styrene copolymer (ABS), the encapsulated nylon of TPE (PA), wherein due to the polarity and TPE material phase of nylon
Difference is larger, so encapsulated difficulty is maximum, the encapsulated difficulty of the PA material of fiberglass reinforced is further up.
Have the defects that TPE is Nian Jie with PA material loosely mostly in the prior art, the TPE material of cladding is easier to from PA base
It removes or falls off on material.Overlap, the defect ware etc. that TPE cover material product generates in process, need the TPE cladding
It is coated again after material removing, the product coated is frequently necessary to recycling secondary use, the existing encapsulated stronger TPE product of performance
A large amount of TPE flexible glue can be remained on substrate when removing PA substrate, the complexity for becoming recovery process reduces nylon products
The rate of recovery.Patent CN103897321A discloses a kind of TPE material of low temperature cladding nylon, the product can 220 DEG C plus
It is bonded nylon at a temperature of work, but a large amount of TPE residual layer can be generated on substrate in stripping process, and to the Buddhist nun of fiberglass reinforced
Dragon does not almost have bonding force.Patent CN103756234A discloses a kind of encapsulated nylon material of TPE for removing noresidue, but it is bonded
Power is limited, and does not almost have bonding force to the nylon of fiberglass reinforced.Patent CN102432976A, which discloses one kind, can coat glass increasing
The thermoplastic elastic of strong nylon, but the product is needed with dimethylbenzene, n-butanol, cyclohexanone mixed liquor before quadric injection mould to nylon
Part carries out spraying pretreatment, and process is complicated, greatly reduces production efficiency, and only to low content glass fiber enhanced nylon (glass
Fine content 25%) there is certain cladding power, it is poor to the cladding power of high-content glass fiber enhanced nylon, it is difficult to practical application.Patent
CN101921444A discloses a kind of removing noresidue, the tack-free special material coated on nylon in surface, but the melting of the product refers to
Number is lower, will lead to the poor mobile performance of the product, needs in process of production big to generate using biggish injection pressure
The overlap of the amount injection defect product more with appearance.
Summary of the invention
Have the defects that TPE is Nian Jie with PA material loosely for solution is of the existing technology, the TPE material of cladding is easier to
The defect removed or fallen off from PA substrate, the present invention provide a kind of for coating the thermoplastic elastomer (TPE) material of glass fiber enhanced nylon
Material and preparation method thereof.
A kind of thermoplastic elastic material coating glass fiber enhanced nylon, which is characterized in that including following mass fraction
Each component:
8~10 parts of styrene block copolymers
20~30 parts of filling oil
20~25 parts of mineral filler
15~25 parts of compatilizer
8.3~23.3 parts of polar resin
5~10 parts of nylon
0~5 part of polar lubricant
0~0.5 part of processing aid
0.2 part of anti-aging agent.
Further, it is preferred that the styrene block copolymers is styrene-butadiene-styrene block
Copolymer (SBS), styrene-isoprene-styrene block copolymer (SIS), styrene-ethylene-butylene-styrene block
Copolymer (SEBS), styrene ethylene-propylene-(SEPS) styrene block copolymer, styrene-ethylene-(ethylene-propylene)-
One of styrene block copolymer (SEEPS) or any several mixture.The preferred styrenic block is total
Polymers is styrene-butadiene-styrene block copolymer, styrene-isoprene-styrene block copolymer and benzene second
The mixture that alkene-ethylene-(ethylene-propylene)-styrene block copolymer is 3~5:1 according to mass ratio, and styrenic block
Styrene-content is 20%-70% in copolymer.The proportion can significantly improve impact resistance and the resistance to brittle fracture energy of product.
Further, the filling oil is one of the saturated straight chain alkane oil of flash-point > 200 DEG C, naphthenic oil or two
The mixture of kind.Preferably, the filling oil is flash-point > 200 DEG C, and initial boiling point is greater than the high aroamtic hydrocarbon raw material oil of 350 DEG C of saturation
Or the mixture of one or both of naphthenic oil.
Further, the mineral filler be calcium carbonate, talcum powder, barium sulfate, kaolin, mica, in montmorillonite
It is at least one.Preferably, it according to mass ratio is 1~3:1 that the mineral filler, which is modified calcium carbonate and modified kaolin, described
The method of modifying of calcium carbonate I be milled under nitrogen or argon partial size be 100~500nm, then under nitrogen protection with
It is to slowly warm up to 400 DEG C under 3~5 DEG C/min, is sintered 4~6h, last mixture 0.1-1% stearic acid;The modifying kaolin
Method is by fineness be 1250-2500 mesh kaolin in 850~920 DEG C of 2~3h of roasting, be then added nano alumina powder and
Sulfuric acid, after mixing evenly successively in 160 DEG C~200 DEG C 15min, 80 DEG C~120 DEG C 30min, 70 DEG C~90 DEG C 30min,
Obtained by 120 DEG C~150 DEG C 15min are reacted.Kaolin is modified using the method for the modified temperature control of multi-temperature zone, significantly
Kaolinic caking property is improved, setting time is short, the characteristic that intensity is high, compensation is shunk.
Modified calcium carbonate and kaolin have flourishing middle macropore pore volume, and adhesive property greatly improves.
Further, the compatilizer is that maleic anhydride is grafted POE (POE-g-MAH), maleic anhydride grafted polyethylene
(PE-g-MAH), maleic anhydride inoculated polypropylene (PP-g-MAH), maleic anhydride grafting ethylene propylene diene rubber (EPDM-g-MAH),
Glycidyl methacrylate graft polyethylene (PE-g-GMA), glycidyl methacrylate graft ethylene propylene diene rubber
(EPDM-g-GMA), maleic anhydride graft phenylethene-ethylene-butylene, Styrene block copolymer (SEBS-g-MAH), alkene are embedding
One of section copolymer (OBC) or any several mixture.Maleic anhydride or glycidyl methacrylate functional group
Grafting rate be 0.5-2.0%.
Further, the polar resin is ethylene-vinyl acetate copolymer (EVA), ethylene-acrylic acid copolymer
(EAA), ethylene-methyl acrylate copolymer (EMA), ethylene methyl methacrylate copolymer (EMMA), ethylene-acrylic acid
One of (EBA), sarin resin or any several mixing in methacrylate copolymers (EEA), ethylene-butyl acrylate copolymer
Object;The melt index of polar resin requires to be greater than 8g/10min (2.16kg counterweight, 190 DEG C).
Further, the nylon is styrene-ethylene-butylene-styrene block copolymer-maleic anhydride-polyamides
Amine terpolymer (SEBS-MAH-PA), block type thermoplastic polyamide elastomer, amorphous nylon, polycaprolactam
(PA6), one of PA 66 (PA66) or any several mixture.
Further, poly- the third of the polar lubricant is grafted for maleic anhydride polyethylene wax, maleic anhydride grafting
One of alkene wax, glycidyl methacrylate graft polyethylene wax, etherificate polyethylene wax, esterification polyethylene wax are any
The weight average molecular weight of several mixtures, polar lubricant is greater than 6000.
Further, the processing aid is erucyl amide, oleamide, N.N '-ethylene bis stearamide, poly- diformazan
At least one of radical siloxane, pentaerythritol stearate.It is according to the present invention to be used to coat glass fiber enhanced nylon
Thermoplastic elastomer (TPE) and preparation method thereof, it is preferred that the anti-aging agent be benzophenone, Hinered phenols, hindered amines,
At least one of phosphorous acid esters can be three (2,4- di-t-butyl) phenyl-phosphites (irgasfos 168), four [β-(3,5- bis-
Tert-butyl-hydroxy phenyl) propionic acid] pentaerythritol ester (antioxidant 1010), β-(3,5- di-tert-butyl-hydroxy phenyl) propionic acid
Octadecanol ester (antioxidant 1076), 1,3,5- trimethyl -2,4,6- three (3,5- di-t-butyl -4- hydroxyl benzyl) benzene (antioxidant
At least one of 330).
It is a kind of for coating the preparation method of the thermoplastic elastic material of glass fiber enhanced nylon, comprising the following steps:
Dry styrene block copolymers and filling oil are sufficiently mixed in high mixer, then again by other materials
It is added in high mixer and is blended, be finally transferred to the extruder melting extrusion for twin-screw totally 12 sections of barrels that draw ratio is 48, melting
160~250 DEG C of Duan Wendu.
Further, melt zone is divided into five areas, the operating temperature in each area are as follows: the first 160-190 DEG C of area, second segment 190
~200 DEG C, 160~180 DEG C of third section, the 4th section 200~230 DEG C, the 5th section 210~250 DEG C.With melt zone in the prior art
The trend that general temperature gradually rises is different, and the present invention can preferably be promoted using different low-high-low-high temperature tendencies
The bonding of section's component, it is ensured that peel strength with higher.
Beneficial effects of the present invention be by being adjusted to the specific selection of styrene block copolymers and proportion, it is right
Mineral material is modified, and adjusts the compatibility of each component, resulting thermoplastic elastic material, cladding glass fiber enhanced nylon bonding
Power is strong, high melt index, good fluidity, has preferable processing performance, and when removing recycling, substrate surface is remained without flexible glue, can
It is widely used in all kinds of handle for tool cladding of glass fiber enhanced nylon substrate.
Specific embodiment
Embodiment 1
First 10 parts of SBS, 25 parts of naphthenic oil are stirred in high mixer and are sufficiently mixed, oil to be filled fully absorb after again
By 20 parts of calcium carbonate, 5 parts of POE-g-MAH, 10 parts of SEBS-g-MAH, 18.3 parts of EVA, 10 parts of polyamide elastane
Body, 1 part of etherificate polyethylene wax, 0.5 part of dimethyl silicone polymer, 0.1 part of antioxidant 1010,0.1 part of irgasfos 168
It is added in high mixer and is blended, be finally transferred to the extruder melting extrusion for twin-screw totally 12 sections of barrels that draw ratio is 48, melting
175 DEG C to 210 DEG C of Duan Wendu, feeding frequency is 25 hertz, and engine speed is 300 revs/min, is granulated particle is dry.
The calcium carbonate is modified calcium carbonate, my ball under nitrogen or argon of the method for modifying that modified method is
Being milled to partial size is 100~500nm, is then sintered 4~6h under nitrogen protection to be to slowly warm up to 400 DEG C under 3~5 DEG C/min,
Last mixture 0.1-1% stearic acid.
Embodiment 2
First 10 parts of SEBS, 20 parts of naphthenic oil are stirred in high mixer and be sufficiently mixed, after oil to be filled fully absorbs
Again by 20 parts of calcium carbonate, 10 parts of EPDM-g-MAH, 10 parts of SEBS-g-MAH, 18.3 parts of EVA, 10 parts of polyamide bullet
Property body, 1 part of etherificate polyethylene wax, 0.5 part of dimethyl silicone polymer, 0.1 part of antioxidant 1010,0.1 part of antioxidant
It is blended in 168 addition high mixers, is finally transferred to the extruder melting extrusion for twin-screw totally 12 sections of barrels that draw ratio is 48, melts
Melt 175 DEG C to 210 DEG C of section temperature, feeding frequency is 25 hertz, and engine speed is 300 revs/min, is granulated particle is dry.
Embodiment 3
First 10 parts of SIS, 28 parts of naphthenic oil are stirred in high mixer and are sufficiently mixed, oil to be filled fully absorb after again
By 22 parts of calcium carbonate, 5 parts of POE-g-MAH, 10 parts of SEBS-g-MAH, 10.3 parts of EMA, 10 parts of polyamide elastane
Body, 1 part of etherificate polyethylene wax, 2 parts of maleic anhydride are grafted PE wax, 0.5 part of dimethyl silicone polymer, 0.1 part of antioxygen
The irgasfos 168 that 1010,0.1 parts of agent is added in high mixer and is blended, and is finally transferred to the twin-screw that draw ratio is 48 totally 12 sections of material
Cylinder extruder melting extrusion, 175 DEG C to 210 DEG C of melt zone temperature, feeding frequency be 25 hertz, engine speed be 300 turns/
Point, it is granulated particle is dry.
Embodiment 4
First 10 parts of SEBS, 22 parts of paraffin oil are stirred in high mixer and be sufficiently mixed, after oil to be filled fully absorbs
Again by 20 parts of calcium carbonate, 5 parts of POE-g-MAH, 10 parts of SEBS-g-MAH, 13.3 parts of EMA, 10 parts of polyamide elastane
Body, 1 part of maleic anhydride grafting PE wax, 0.5 part of pentaerythritol stearate, 0.1 part of antioxidant 1010,0.1 part anti-
Oxygen agent 168 is added in high mixer and is blended, and the extruder melting for being finally transferred to the twin-screw that draw ratio is 48 totally 12 sections of barrels is squeezed
Out, 175 DEG C to 210 DEG C of melt zone temperature, feeding frequency are 25 hertz, and engine speed is 300 revs/min, are granulated particle is dry.
Embodiment 5
First 10 parts of SEBS, 24 parts of paraffin oil are stirred in high mixer and be sufficiently mixed, after oil to be filled fully absorbs
Again by 20 parts of calcium carbonate, 5 parts of POE-g-MAH, 5 parts of EPDM-g-GMA, 10 parts of SEBS-g-MAH, 23.3 parts
EMMA, 5 parts of polyamide elastomer, 1 part of maleic anhydride grafting PE wax, 0.5 part of dimethyl silicone polymer, 0.1 part anti-
The irgasfos 168 that 1010,0.1 parts of oxygen agent is added in high mixer and is blended, and is finally transferred to totally 12 sections of twin-screw that draw ratio is 48
The extruder melting extrusion of barrel, 175 DEG C to 210 DEG C of melt zone temperature, feeding frequency be 25 hertz, engine speed be 300 turns/
Point, it is granulated particle is dry.
Embodiment 6
First 8 parts of SEBS, 25 parts of paraffin oil are stirred in high mixer and are sufficiently mixed, oil to be filled fully absorb after again
By 20 parts of calcium carbonate, 10 parts of PE-g-MAH, 15 parts of SEBS-g-MAH, 9.3 parts of EMMA, 10 parts of polyamide elastane
Body, 2 parts of etherificate polyethylene wax, 0.5 part of dimethyl silicone polymer, 0.1 part of antioxidant 1010,0.1 part of irgasfos 168
It is added in high mixer and is blended, be finally transferred to the extruder melting extrusion for twin-screw totally 12 sections of barrels that draw ratio is 48, melting
175 DEG C to 210 DEG C of Duan Wendu, feeding frequency is 25 hertz, and engine speed is 300 revs/min, is granulated particle is dry.
Embodiment 7
First by 8 parts of styrene block copolymers, 28 parts of flash-point > 200 DEG C, saturation of the initial boiling point greater than 350 DEG C is high
Aroamtic hydrocarbon raw material oil is stirred in high mixer and is sufficiently mixed, oil to be filled fully absorb after again by 25 parts of modified calcium carbonate, 5 parts
Modified kaolin, 10 parts of POE-g-MAH, 5 parts of PE-g-MAH, 10 parts of SEBS-g-MAH, 8.3 parts of EMMA, 5 parts of ether
Change polyethylene wax, 0.5 part of dimethyl silicone polymer, 0.1 part of antioxidant 1010,0.1 part of irgasfos 168 and high mixer is added
Middle blending, is finally transferred to the extruder melting extrusion for twin-screw totally 12 sections of barrels that draw ratio is 48, and 175 DEG C of melt zone temperature
To 210 DEG C, feeding frequency is 25 hertz, and engine speed is 300 revs/min, is granulated particle is dry.
The styrene block copolymers is the mixture that SBS, SIS and SEEPS are 3~5:1 according to mass ratio, and
Styrene-content is 20%-70% in styrene block copolymers.
The calcium carbonate is modified calcium carbonate, my ball under nitrogen or argon of the method for modifying that modified method is
Being milled to partial size is 100~500nm, is then sintered 4~6h under nitrogen protection to be to slowly warm up to 400 DEG C under 3~5 DEG C/min,
Last mixture 0.1-1% stearic acid.
The improvement of kaolin is by fineness be 1250-2500 mesh kaolin 850~920 DEG C roast 2~
Then nano alumina powder and sulfuric acid is added in 3h, after mixing evenly successively in 160 DEG C~200 DEG C 15min, 80 DEG C~120 DEG C
30min, 70 DEG C~90 DEG C 30min, obtained by 120 DEG C~150 DEG C 15min are reacted.
Embodiment 8
First 10 parts of SEBS, 25 parts of paraffin oil are stirred in high mixer and be sufficiently mixed, after oil to be filled fully absorbs
Again by 20 parts of calcium carbonate, 5 parts of POE-g-MAH, 5 parts of OBC, 10 parts of SEBS-g-MAH, 9.3 parts of EMMA, 5 parts of ether
Change polyethylene wax, 0.5 part of dimethyl silicone polymer, 0.1 part of antioxidant 1010,0.1 part of irgasfos 168 and high mixer is added
Middle blending, is finally transferred to the extruder melting extrusion for twin-screw totally 12 sections of barrels that draw ratio is 48, and 175 DEG C of melt zone temperature
To 210 DEG C, feeding frequency is 25 hertz, and engine speed is 300 revs/min, is granulated particle is dry.
Embodiment 9
First 10 parts of SEEPS, 25 parts of naphthenic oil are stirred in high mixer and be sufficiently mixed, after oil to be filled fully absorbs
Again by 20 parts of calcium carbonate, 5 parts of POE-g-MAH, 5 parts of PE-g-MAH, 10 parts of SEBS-g-MAH, 9.3 parts of EMMA, 10
Part PA6,5 parts of etherificate polyethylene wax, 0.5 part of pentaerythritol stearate, 0.1 part of antioxidant 1010,0.1 part anti-
Oxygen agent 168 is added in high mixer and is blended, and the extruder melting for being finally transferred to the twin-screw that draw ratio is 48 totally 12 sections of barrels is squeezed
Out, 175 DEG C to 210 DEG C of melt zone temperature, feeding frequency are 25 hertz, and engine speed is 300 revs/min, are granulated particle is dry.
Embodiment 10
First 10 parts of SEPS, 25 parts of paraffin oil are stirred in high mixer and be sufficiently mixed, after oil to be filled fully absorbs
Again by 20 parts of calcium carbonate, 10 parts of PE-g-MAH, 10 parts of SEBS-g-MAH, 9.3 parts of EMMA, 10 parts of PA6,5 parts
It is etherified polyethylene wax, 0.5 part of pentaerythritol stearate, 0.1 part of antioxidant 1010,0.1 part of irgasfos 168 and height is added
It is blended in mixed machine, is finally transferred to the extruder melting extrusion of the twin-screw that draw ratio is 48 totally 12 sections of barrels, melt zone temperature
175 DEG C to 210 DEG C, feeding frequency is 25 hertz, and engine speed is 300 revs/min, is granulated particle is dry.
Comparative example 1
First 10 parts of SEBS, 25 parts of paraffin oil are stirred in high mixer and be sufficiently mixed, after oil to be filled fully absorbs
Again by 25 parts of calcium carbonate, 5 parts of POE-g-MAH, 5 parts of PE-g-MAH, 10 parts of SEBS-g-MAH, 9.3 parts of EMMA, 10
Part PA6,5 parts of etherificate polyethylene wax, 0.5 part of pentaerythritol stearate, 0.1 part of antioxidant 1010,0.1 part anti-
Oxygen agent 168 is added in high mixer and is blended, and the extruder melting for being finally transferred to the twin-screw that draw ratio is 48 totally 12 sections of barrels is squeezed
Out, 175 DEG C to 210 DEG C of melt zone temperature, feeding frequency are 25 hertz, and engine speed is 300 revs/min, are granulated particle is dry.
Comparative example 2
First 10 parts of SEBS, 25 parts of naphthenic oil are stirred in high mixer and be sufficiently mixed, after oil to be filled fully absorbs
Again by 25 parts of calcium carbonate, 10 parts of POE-g-MAH, 10 parts of SEBS-g-MAH, 17.8 parts of EMA, 10 parts of PA6,2 parts
Maleic anhydride grafting PE wax, 0.1 part of antioxidant 1010,0.1 part of irgasfos 168 are added in high mixer and are blended, and finally shift
To the extruder melting extrusion for twin-screw totally 12 sections of barrels that draw ratio is 48,175 DEG C to 210 DEG C of melt zone temperature, feeding frequency
Rate is 25 hertz, and engine speed is 300 revs/min, is granulated particle is dry.
1 material peel strength test tables of data of table
The peel strength of cladding enhancing nylon PP Pipe Compound of the invention is high as can be seen from Table 1, significantly larger than the prior art,
The melt index of sample is higher, is conducive to processing, and embodiment 2 and comparative example 7 are removed the comparison of rear substrate residual it can be found that implementing
Residual of 7 substrate surface of example without flexible glue, improves recovery efficiency, and the comprehensive mechanical property of sample is excellent, is able to satisfy absolutely mostly
The cladding demand of number glass fiber enhanced nylon handle for tool.
The above is only the preferred embodiments of the invention, it is noted that for the ordinary skill people of the art
Member, under the premise of not departing from the method for the present invention, can also make several improvement and supplement, these are improved and supplement also should be regarded as
Protection scope of the present invention.
Claims (10)
1. a kind of thermoplastic elastic material for coating glass fiber enhanced nylon, which is characterized in that including each of following mass fraction
Component:
8~10 parts of styrene block copolymers
20~30 parts of filling oil
20~25 parts of mineral filler
15~25 parts of compatilizer
8.3~23.3 parts of polar resin
5~10 parts of nylon
0~5 part of polar lubricant
0~0.5 part of processing aid
0.2 part of anti-aging agent.
2. the thermoplastic elastic material of cladding glass fiber enhanced nylon as described in claim 1, which is characterized in that the benzene
Ethylene based block copolymer is styrene-butadiene-styrene block copolymer, styrene-isoprene-phenylethene block
The mixture that copolymer and styrene-ethylene-(ethylene-propylene)-styrene block copolymer are 3~5:1 according to mass ratio, and
Styrene-content is 20%-70% in styrene block copolymers.
3. the thermoplastic elastic material of cladding glass fiber enhanced nylon as described in claim 1, which is characterized in that described fills out
Oil-filled is flash-point > 200 DEG C, and initial boiling point is saturated the mixed of one or both of high aroamtic hydrocarbon raw material oil or naphthenic oil greater than 350 DEG C
Close object.
4. the thermoplastic elastic material of cladding glass fiber enhanced nylon as described in claim 1, which is characterized in that the mine
It according to mass ratio is 1~3:1 that object filler, which is modified calcium carbonate and modified kaolin, the method for modifying of the calcium carbonate I in nitrogen
Or being milled to partial size under argon gas protection is 100~500nm, then under nitrogen protection to be to slowly warm up under 3~5 DEG C/min
400 DEG C, it is sintered 4~6h, last mixture 0.1-1% stearic acid;It is 1250-2500 that the improvement of kaolin, which is by fineness,
Then purpose kaolin is added nano alumina powder and sulfuric acid, successively exists after mixing evenly in 850~920 DEG C of 2~3h of roasting
160 DEG C~200 DEG C 15min, 80 DEG C~120 DEG C 30min, 70 DEG C~90 DEG C 30min, 120 DEG C~150 DEG C 15min are reacted
Gained.
5. the thermoplastic elastic material of cladding glass fiber enhanced nylon as described in claim 1, which is characterized in that the phase
It is poly- for maleic anhydride grafting POE (POE-g-MAH), maleic anhydride grafted polyethylene (PE-g-MAH), maleic anhydride grafting to hold agent
Propylene (PP-g-MAH), maleic anhydride are grafted ethylene propylene diene rubber (EPDM-g-MAH), glycidyl methacrylate graft
Polyethylene (PE-g-GMA), glycidyl methacrylate graft ethylene propylene diene rubber (EPDM-g-GMA), maleic anhydride connect
Branch styrene-ethylene-butylene-styrene block copolymer (SEBS-g-MAH), one of olefin block copolymers (OBC) or
Any several mixture.
6. the thermoplastic elastic material of cladding glass fiber enhanced nylon as described in claim 1, which is characterized in that the pole
Property resin be ethylene-vinyl acetate copolymer (EVA), ethylene-acrylic acid copolymer (EAA), ethylene-methyl acrylate copolymerization
Object (EMA), ethylene methyl methacrylate copolymer (EMMA), ethylene-ethyl acrylate copolymer (EEA), ethylene-propylene
One of (EBA), sarin resin or any several mixture in butyl acrylate copolymer.
7. the thermoplastic elastic material of cladding glass fiber enhanced nylon as described in claim 1, which is characterized in that the Buddhist nun
Dragon be styrene-ethylene-butylene-styrene block copolymer-maleic anhydride-polyamide terpolymer (SEBS-MAH-PA),
Block type thermoplastic polyamide elastomer, amorphous nylon, polycaprolactam (PA6), in PA 66 (PA66)
The mixture of one or any of several.
8. the thermoplastic elastic material of cladding glass fiber enhanced nylon as described in claim 1, which is characterized in that the pole
Property lubricant be maleic anhydride grafting polyethylene wax, maleic anhydride grafting polypropylene wax, glycidyl methacrylate
One of grafted polyethylene wax, etherificate polyethylene wax, esterification polyethylene wax or any several mixture.
9. a kind of as claim 1-8 is described in any item for coating the system of the thermoplastic elastic material of glass fiber enhanced nylon
Preparation Method, which comprises the following steps:
Dry styrene block copolymers and filling oil are sufficiently mixed in high mixer, then other materials are added again
It is blended in high mixer, is finally transferred to the extruder melting extrusion for twin-screw totally 12 sections of barrels that draw ratio is 48, melt zone temperature
160~250 DEG C of degree.
10. it is as claimed in claim 9 for coating the preparation method of the thermoplastic elastic material of glass fiber enhanced nylon, it is special
Sign is that melt zone is divided into five areas, the operating temperature in each area are as follows: the first 190-200 DEG C of area, 170~190 DEG C of second segment,
Three sections 160~180 DEG C, the 4th section 200~230 DEG C, the 5th section 210~250 DEG C.
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