CN107955282A - A kind of PS composite materials - Google Patents

A kind of PS composite materials Download PDF

Info

Publication number
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
Authority
CN
China
Prior art keywords
composite materials
tio
parts
graphene
materials according
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
CN201711112855.3A
Other languages
Chinese (zh)
Inventor
薛亚红
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to CN201711112855.3A priority Critical patent/CN107955282A/en
Publication of CN107955282A publication Critical patent/CN107955282A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F292/00Macromolecular compounds obtained by polymerising monomers on to inorganic materials
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00Compositions 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
    • C08L25/02Homopolymers or copolymers of hydrocarbons
    • C08L25/04Homopolymers or copolymers of styrene
    • C08L25/06Polystyrene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/017Additives being an antistatic agent
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/04Antistatic

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

A kind of PS composite materials
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)

  1. 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. 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. 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. 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. 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. 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. 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.
CN201711112855.3A 2017-11-10 2017-11-10 A kind of PS composite materials Pending CN107955282A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201711112855.3A CN107955282A (en) 2017-11-10 2017-11-10 A kind of PS composite materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201711112855.3A CN107955282A (en) 2017-11-10 2017-11-10 A kind of PS composite materials

Publications (1)

Publication Number Publication Date
CN107955282A true CN107955282A (en) 2018-04-24

Family

ID=61963629

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201711112855.3A Pending CN107955282A (en) 2017-11-10 2017-11-10 A kind of PS composite materials

Country Status (1)

Country Link
CN (1) CN107955282A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
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

Cited By (2)

* Cited by examiner, † Cited by third party
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

Similar Documents

Publication Publication Date Title
CN106750988B (en) A kind of PPR pipe and preparation method thereof with excellent low temperature toughness
CN103626911B (en) A kind of hydrophobicity organic-inorganic high silicon content acrylate polymer emulsion and preparation method thereof and application
CN103059681B (en) Water-based quick-drying external crosslinking functional paint and preparation method thereof
CN105820276A (en) Preparation method of ultrahigh-conductivity graphene modified polymethyl methacrylate composite material
CN103059212A (en) Hydrogenated rosin modified acrylic ester hybridization emulsion and preparation method and application thereof
CN106479072B (en) A kind of PS composite material and preparation methods
CN103044614A (en) Preparation method for silane coupling agent modified acrylic ester
CN107955282A (en) A kind of PS composite materials
CN105315820A (en) Waterproofing acid-proofing anti-collision insulating coating
CN105294927A (en) Butyl acrylate/butadiene/styrene latex and preparation method thereof
CN104387909A (en) Thinly-coated-type corrosion-resistant modified floor coating and preparation method thereof
CN102050929A (en) Elastic emulsion prepared from water-soluble polyurethane and acrylic acid by hybrid polymerization
CN109942969A (en) A kind of PS composite material
CN106046572A (en) Modified mica/polypropylene composite plastic
CN103936911B (en) The preparation method of dumbbell shaped Janus colloidal particle
CN105018910B (en) A kind of method of preparing super oleophobic surface taking kaolin as raw material
CN104087106A (en) Preparation method of light-resistant water-based paint and adhesive
CN100462379C (en) Preparation method of ultraviolet light stabilizer
CN106633384A (en) Scratch-resistant anti-microbial high-performance anti-flaming PP composite material and preparation method thereof
CN109942931A (en) A kind of high performance PE composite material
CN104893454A (en) Heat preservation material
CN105238127A (en) Non-baking anti-fingerprint coating additive and using method thereof
CN109679331A (en) A kind of 6 composite material of static resistant polyamide
CN105925217B (en) A kind of polyvinyl acetate emulsion binding agent
CN103740225B (en) A kind of preparation method of modification acrylate protective system

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20180424

WD01 Invention patent application deemed withdrawn after publication