CN107955282A - A kind of PS composite materials - Google Patents
A kind of PS composite materials Download PDFInfo
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- CN107955282A CN107955282A CN201711112855.3A CN201711112855A CN107955282A CN 107955282 A CN107955282 A CN 107955282A CN 201711112855 A CN201711112855 A CN 201711112855A CN 107955282 A CN107955282 A CN 107955282A
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- composite materials
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- graphene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F292/00—Macromolecular compounds obtained by polymerising monomers on to inorganic materials
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/06—Polystyrene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/017—Additives being an antistatic agent
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/04—Antistatic
Abstract
The present invention relates to a kind of PS composite materials, it is made of the component of following parts by weight:PS is 60 parts 80 parts;ABS is 10 parts 20 parts;TiO2G P (GMA AN) are 6 parts 24 parts;The graphene of processing is 8 parts 12 parts;Antioxidant is 0.1 part 0.5 part;Lubricant is 0.1 part 0.3 part.For the technical program using the oxygen-containing functional group on the surface of graphene, in surface grafting, suitable long chain alkane, long chain alkane can effectively stop the reunion of graphene by way of chemical bonding, and graphene can be better dispersed in PS composite materials.The technical program is in TiO2GMA, AN are grafted on surface, one side P (GMA AN) is connected to TiO with chemical bond2, surface grafting rate higher, is conducive to stress to be transmitted on particle, and another aspect surface grafting thing can improve TiO2With PS compatibilities.
Description
Technical field
The invention belongs to technical field of polymer materials, particularly relates to a kind of PS composite materials.
Background technology
Polystyrene (PS) has light, nontoxic, odorless, and chemical stability is good, and electrical insulation capability is good, and at normal temperatures not
Common solvent is dissolved in, the advantages that water imbibition is small.Although the comprehensive performance of PS is very excellent, in some specific application necks
Domain, the physical property of PS, often do not reach certain requirement, and which greatly limits the application range of PS.
The content of the invention
The object of the present invention is to provide a kind of PS composite materials and preparation method thereof, to improve the physical of PS composite materials
Energy.
The present invention is achieved by the following technical solutions:
A kind of PS composite materials, are made of the component of following parts by weight:
The TiO2The preparation method of-g-P (GMA-AN), comprises the following steps:
1) by TiO2, lauryl sodium sulfate, polyoxyethylene nonylphenol ether 10, deionized water be placed in ultrasonic disperse 6- in four-hole boiling flask
10h, adds the potassium peroxydisulfate of certain mass, 80-120 DEG C of reaction 4-6h, obtains mixed solution A;
2) glycidyl methacrylate, acrylonitrile are added into four-hole boiling flask, are mixed with mixed solution A,
120-160 DEG C of reaction 8-12h, obtains mixed solution B;
3) by mixed solution B filtration washings, white product is obtained, 80-100 DEG C of reaction 6-8h is up to product TiO2-g-P
(GMA-AN)。
The TiO2, lauryl sodium sulfate, the polyoxyethylene nonylphenol ether 10, the deionized water and the potassium peroxydisulfate
Mass ratio be 20-30: 0.1-0.3: 0.2-0.4: 200-280: 1-3.
The mass ratio of the glycidyl methacrylate, the acrylonitrile and the mixed solution A is 12-16: 10-14
∶230-260。
The graphene is the graphene after processing, and the processing method of the graphene after the processing comprises the following steps:
1) weigh octadecylamine, ethanol is added into the aqueous solution of graphene, under 100-120 DEG C of oil bath pan environment, return
Stream reaction 20-24h;
2) step 1) products therefrom is filtered, is placed in 60-80 DEG C of vacuum tank dry 20-24h, the stone after must both handling
Black alkene.
The mass ratio of the octadecylamine, the ethanol and the graphene is 20-28: 50-60: 100-160.
The antioxidant is three (2,4- di-t-butyl) phenyl-phosphites, four [β-(3,5- di-tert-butyl-hydroxy phenyls)
Propionic acid] pentaerythritol ester or 1,3,5- trimethyls -2,4, one kind or more in 6- (3,5- di-t-butyl -4- hydroxyphenylmethyls) benzene
Kind.
The lubricant is the one or more in zinc stearate, calcium stearate or potassium stearate.
The beneficial effects of the invention are as follows:
The technical program utilizes the oxygen-containing functional group on the surface of graphene, in surface grafting by way of chemical bonding
Suitable long chain alkane, long chain alkane can effectively stop the reunion of graphene, allow graphene to be better dispersed in PS and answer
In condensation material.The addition of graphene can lift the antistatic property in PS composite materials at the same time.
The technical program is in TiO2GMA, AN are grafted on surface, compared to directly adding TiO2, physical property is more preferable, this is
Because one side P (GMA-AN) is connected to TiO with chemical bond2, surface grafting rate higher, is conducive to stress to be transmitted to particle
On, another aspect surface grafting thing can improve TiO2With PS compatibilities.
Embodiment
Carry out the technical solution that the present invention will be described in detail by the following examples, following embodiment is only exemplary, only
It can be used for explanation and illustration technical scheme, and be not to be construed as the limitation to technical solution of the present invention.
Embodiment 1
1) 60 parts of PS, 10 parts of ABS, 16 parts of TiO are weighed2- g-P (GMA-AN), 8 parts of graphenes, 0.1 part of Irganox168,
0.1 part of calcium stearate is mixed and stirred for uniformly, obtaining mixture;
2) the mixture extruding pelletization that will be obtained in step 1), that is, obtain PS composite materials P1.
Wherein, double screw extruder includes six humidity provinces sequentially arranged, and the temperature of the first humidity province is 140 DEG C, the
The temperature of two humidity provinces is 180 DEG C, and the temperature of the 3rd humidity province is 180 DEG C, and the temperature of the 4th humidity province is 180 DEG C, the 5th temperature
The temperature for spending area is 180 DEG C, and the temperature of the 6th humidity province is 180 DEG C, and the head temperature of double screw extruder is 180 DEG C, screw rod
Rotating speed is 200r/min.
Embodiment 2
1) 80 parts of PS, 20 parts of ABS, 24 parts of TiO are weighed2- g-P (GMA-AN), 8 parts of graphenes, 0.1 part of Irganox1010,
0.2 part of Irganox1330,0.2 part of Irganox168,0.3 part of odium stearate are mixed and stirred for uniformly, obtaining mixture;
2) the mixture extruding pelletization that will be obtained in step 1), that is, obtain PS composite materials P2.
Wherein, double screw extruder includes six humidity provinces sequentially arranged, and the temperature of the first humidity province is 160 DEG C, the
The temperature of two humidity provinces is 220 DEG C, and the temperature of the 3rd humidity province is 220 DEG C, and the temperature of the 4th humidity province is 220 DEG C, the 5th temperature
The temperature for spending area is 220 DEG C, and the temperature of the 6th humidity province is 220 DEG C, and the head temperature of double screw extruder is 220 DEG C, screw rod
Rotating speed is 260r/min.
Embodiment 3
1) 70 parts of PS, 15 parts of ABS, 20 parts of TiO are weighed2- g-P (GMA-AN), 10 parts of graphenes, 0.3 part
Irganox1330,0.2 part of potassium stearate are mixed and stirred for uniformly, obtaining mixture;
2) the mixture extruding pelletization that will be obtained in step 1), that is, obtain PS composite materials P3.
Wherein, double screw extruder includes six humidity provinces sequentially arranged, and the temperature of the first humidity province is 150 DEG C, the
The temperature of two humidity provinces is 200 DEG C, and the temperature of the 3rd humidity province is 200 DEG C, and the temperature of the 4th humidity province is 200 DEG C, the 5th temperature
The temperature for spending area is 200 DEG C, and the temperature of the 6th humidity province is 200 DEG C, and the head temperature of double screw extruder is 200 DEG C, screw rod
Rotating speed is 230r/min.
It the above is only the description of the preferred embodiment of the present invention, it is noted that due to the finiteness of literal expression, and
Objectively there are unlimited concrete structure, for those skilled in the art, the principle of the invention is not being departed from
On the premise of, some improvements and modifications can also be made, these improvements and modifications also should be regarded as protection scope of the present invention.
Claims (7)
- A kind of 1. PS composite materials, it is characterised in that:It is made of the component of following parts by weight:The TiO2The preparation method of-g-P (GMA-AN), comprises the following steps:1) by TiO2, lauryl sodium sulfate, polyoxyethylene nonylphenol ether 10, deionized water be placed in ultrasonic disperse 6-10h in four-hole boiling flask, then The potassium peroxydisulfate of certain mass is added, 80-120 DEG C of reaction 4-6h, obtains mixed solution A;2) glycidyl methacrylate, acrylonitrile are added into four-hole boiling flask, is mixed with mixed solution A, 120-160 DEG C reaction 8-12h, obtain mixed solution B;3) by mixed solution B filtration washings, white product is obtained, 80-100 DEG C of reaction 6-8h is up to product TiO2-g-P(GMA- AN)。
- 2. PS composite materials according to claim 1, it is characterised in that:The TiO2, the lauryl sodium sulfate, institute The mass ratio for stating polyoxyethylene nonylphenol ether 10, the deionized water and the potassium peroxydisulfate is 20-30: 0.1-0.3: 0.2-0.4: 200- 280∶1-3。
- 3. PS composite materials according to claim 1, it is characterised in that:The glycidyl methacrylate, described third Alkene is fine and the mass ratio of the mixed solution A is 12-16: 10-14: 230-260.
- 4. PS composite materials according to claim 1, it is characterised in that:The graphene for processing after graphene, institute The processing method for stating the graphene after processing comprises the following steps:1) weigh octadecylamine, ethanol is added into the aqueous solution of graphene, under 100-120 DEG C of oil bath pan environment, reflux is anti- Answer 20-24h;2) step 1) products therefrom is filtered, is placed in 60-80 DEG C of vacuum tank dry 20-24h, the graphite after must both handling Alkene.
- 5. PS composite materials according to claim 4, it is characterised in that:The octadecylamine, the ethanol and the graphite The mass ratio of alkene is 20-28: 50-60: 100-160.
- 6. PS composite materials according to claim 1, it is characterised in that:The antioxidant is sub- for three (2,4- di-t-butyls) Phenyl phosphate, four [β-(3,5- di-tert-butyl-hydroxy phenyl) propionic acid] pentaerythritol esters or 1,3,5- trimethyls -2,4,6- One or more in (3,5- di-t-butyl -4- hydroxyphenylmethyls) benzene.
- 7. PS composite materials according to claim 1, it is characterised in that:The lubricant is zinc stearate, calcium stearate Or the one or more in potassium stearate.
Priority Applications (1)
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CN201711112855.3A CN107955282A (en) | 2017-11-10 | 2017-11-10 | A kind of PS composite materials |
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CN201711112855.3A CN107955282A (en) | 2017-11-10 | 2017-11-10 | A kind of PS composite materials |
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CN107955282A true CN107955282A (en) | 2018-04-24 |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112250984A (en) * | 2020-08-28 | 2021-01-22 | 东莞市建荣电子塑胶有限公司 | Injection molding process of automotive interior trim part |
-
2017
- 2017-11-10 CN CN201711112855.3A patent/CN107955282A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112250984A (en) * | 2020-08-28 | 2021-01-22 | 东莞市建荣电子塑胶有限公司 | Injection molding process of automotive interior trim part |
CN112250984B (en) * | 2020-08-28 | 2021-08-20 | 东莞市建荣电子塑胶有限公司 | Injection molding process of automotive interior trim part |
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