CN108752880A - A kind of PBT composite and preparation method thereof - Google Patents

A kind of PBT composite and preparation method thereof Download PDF

Info

Publication number
CN108752880A
CN108752880A CN201810638159.4A CN201810638159A CN108752880A CN 108752880 A CN108752880 A CN 108752880A CN 201810638159 A CN201810638159 A CN 201810638159A CN 108752880 A CN108752880 A CN 108752880A
Authority
CN
China
Prior art keywords
parts
pbt
temperature
pbt composite
area
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
CN201810638159.4A
Other languages
Chinese (zh)
Inventor
刘凯
吴向东
孙启林
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.)
Anhui Jianghuai Automobile Group Corp
Original Assignee
Anhui Jianghuai Automobile Group Corp
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 Anhui Jianghuai Automobile Group Corp filed Critical Anhui Jianghuai Automobile Group Corp
Priority to CN201810638159.4A priority Critical patent/CN108752880A/en
Publication of CN108752880A publication Critical patent/CN108752880A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/20Compounding polymers with additives, e.g. colouring
    • C08J3/22Compounding polymers with additives, e.g. colouring using masterbatch techniques
    • C08J3/226Compounding polymers with additives, e.g. colouring using masterbatch techniques using a polymer as a carrier
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2367/00Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
    • C08J2367/02Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2467/00Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
    • C08J2467/02Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2483/00Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
    • C08J2483/04Polysiloxanes
    • 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
    • C08K13/00Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
    • C08K13/04Ingredients characterised by their shape and organic or inorganic ingredients
    • 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
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/13Phenols; Phenolates
    • C08K5/134Phenols containing ester groups
    • C08K5/1345Carboxylic esters of phenolcarboxylic acids
    • 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
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/20Carboxylic acid amides
    • 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
    • C08K5/00Use of organic ingredients
    • C08K5/49Phosphorus-containing compounds
    • C08K5/51Phosphorus bound to oxygen
    • C08K5/52Phosphorus bound to oxygen only
    • C08K5/524Esters of phosphorous acids, e.g. of H3PO3
    • C08K5/526Esters of phosphorous acids, e.g. of H3PO3 with hydroxyaryl compounds
    • 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
    • C08K7/00Use of ingredients characterised by shape
    • C08K7/02Fibres or whiskers
    • C08K7/04Fibres or whiskers inorganic
    • C08K7/14Glass

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The present invention relates to a kind of PBT composite and preparation method thereof, weigh 60 parts -80 parts PBT, 50 parts of -60 parts of glass fibres, 0.1 part of -0.3 part of SEBS-g-MAH, 2 parts of -6 parts of glossiness modified master batch, 0.1 part of -0.3 part of Chimassob, 2020,0.1 parts of -0.5 part of antioxidant;Obtained mixture extruding pelletization is to get to PBT composite.Glossiness modified master batch mechanism, silicone powder improve glass in the dispersibility of PBT base-materials, improve the interface compatibility of glass and PBT base-materials, are conducive to improve apparent mass;The addition of melting means modifier CBT-100 improves the melt index of PBT base-materials, the flow resistances of PBT in the molten state is reduced, so as to improve apparent mass.

Description

A kind of PBT composite and preparation method thereof
Technical field
The invention belongs to technical field of polymer materials, a kind of PBT composite and preparation method thereof is particularly related to.
Background technology
Polybutylene terephthalate (PBT) (PBT) is a kind of important thermoplastic material, is widely used in automobile, household electric The fields such as device, mechanical fitting, office appliance and Communication Equipment.PBT material have it is light, nontoxic, odorless, good water absorption etc. is excellent Point.
A kind of excellent in mechanical performance, apparent mass, the good PBT composite of weather resistance is made in the application innovation, This material not yet sees report so far, this has very important realistic meaning for the application for extending PBT composite.
Invention content
The object of the present invention is to provide a kind of PBT composites and preparation method thereof, to improve the physics of PBT composite Performance and weather resistance.
The present invention is achieved by the following technical solutions:
A kind of PBT composite, it is composed of the following components by weight:
The compatilizer is SEBS-g-MAH.
The glossiness modified master batch, is made of the component of following parts by weight:
The melting means modifier is mobility modifying agent CBT-100.
The coupling agent is titanate coupling agent AC-201.
The lubricant is erucyl amide.
The preparation process of the glossiness modified master batch is:
(1) 60 parts of -80 parts of PBT, 10 parts of -16 parts of silicone powders, 16 parts of -20 parts of CBT-100,0.1 part of -0.3 part of AC- are weighed 201,0.1 part of -0.5 part of erucyl amide;
(2) by the mixture extruding pelletization obtained in step (1) to get to glossiness modified master batch.
The light stabilizer is Chimassob 2020.
The antioxidant is three (2,4- di-t-butyl) phenyl-phosphites, four [β-(3,5- di-tert-butyl-hydroxy phenyl) Propionic acid] pentaerythritol ester or 1,3,5- trimethyls -2,4, one kind or several in 6- (3,5- di-t-butyl -4- hydroxyphenylmethyls) benzene The mixing of kind.
The preparation method of any of the above-described PBT composite, includes the following steps:
(1) weigh 60 parts -80 parts PBT, 50 parts of -60 parts of glass fibres, 0.1 part of -0.3 part of SEBS-g-MAH, 2 parts -6 parts Glossiness modified master batch, 0.1 part of -0.3 part of Chimassob, 2020,0.1 parts of -0.5 part of antioxidant;
(2) by the mixture extruding pelletization obtained in step (1) to get to PBT composite.
The beneficial effects of the invention are as follows:
1, glossiness modified master batch mechanism:1. silicone powder improve glass PBT base-materials dispersibility, improve glass with The interface compatibility of PBT base-materials is conducive to improve apparent mass.2. the addition of melting means modifier CBT-100 improves PBT base-materials Melt index, PBT flow resistances in the molten state are reduced, so as to improve apparent mass.
2, the compounding of antioxidant and light stabilizer enhances the weatherability of PBT composite.
3, the PBT composite of high glass fiber content made from the application, excellent physical properties, apparent mass, weather resistance Well, there is good promotional value.
Specific implementation mode
Carry out the technical solution that the present invention will be described in detail by the following examples, embodiment below is merely exemplary, only It can be used for explanation and illustration technical scheme of the present invention, and be not to be construed as the limitation to technical solution of the present invention.
Raw material is as follows used in the following embodiment of the application:
PBT (model 2002U), Polyplastics;Glass fibre (model T438H), Taishan glass fiber Ltd;Silicone Powder, China Bluestar Chengrand Research Institute of Chemical Industry Co., Ltd.;Light stabilizer (model C himassob 2020), BASF AG;It is anti- Oxygen agent (model Irganox168, Irganox1010, Irganox1330), Switzerland's Ciba;SEBS-g-MAH, the match of Suzhou Asia It is plasticized Co., Ltd.
Test equipment used in the following embodiment of the application is as follows:
ZSK30 type double screw extruders, German W&P companies;JL-1000 type tensile testing machines, the wide just experiment instrument in Guangzhou Device company produces;HTL900-T-5B type injection (mo(u)lding) machines, the production of Hai Tai plastics machineries Co., Ltd;XCJ-500 type shock-testings Machine, the production of Chengde testing machine factory;QT-1196 type tester for elongation, Dongguan City Gao Tai detecting instruments Co., Ltd;QD-GJS- B12K type homogenizers, Beijing perseverance Order instrument and meter Co., Ltd;101A-1 type digital display Electric heat ovens, the holy glad science in Shanghai Instrument Ltd..
The application provides a kind of PBT composite, composed of the following components by weight:
Glass fiber diameter is 4-8 μm;Wherein compatilizer is SEBS-g-MAH;Light stabilizer is BASF AG's production Chimassob 2020。
Antioxidant is three (2,4- di-t-butyls) phenyl-phosphites (abbreviation Irganox168), the four [β-of BASF AG (3,5- di-tert-butyl-hydroxy phenyl) propionic acid] pentaerythritol ester (abbreviation Irganox1010) or 1,3,5- trimethyls -2,4, The mixing of one or more of 6- (3,5- di-t-butyl -4- hydroxyphenylmethyls) benzene (abbreviation Irganox1330).
Glossiness modified master batch is made of the component of following parts by weight:
PBT is the PBT 2002U of Polyplastics production;Melting means modifier is the mobility modifying agent that the source of Dongguan wound produces CBT-100;Coupling agent is the titanate coupling agent AC-201 that Nanjing Olympic really produces;Lubricant is erucyl amide.
The preparation process of glossiness modified master batch is:
(1) 60 parts of -80 parts of PBT, 10 parts of -16 parts of silicone powders, 16 parts of -20 parts of CBT-100,0.1 part of -0.3 part of AC- are weighed 201,0.1 part of -0.5 part of erucyl amide;
(2) by the mixture extruding pelletization obtained in step (1) to get to glossiness modified master batch.
Double screw extruder in step (2) includes six humidity provinces sequentially arranged, 200~220 DEG C of area's temperature, and two 240~260 DEG C of area's temperature, three 240~260 DEG C of area's temperature, four 240~260 DEG C of area's temperature, five 240~260 DEG C of area's temperature, six 240~260 DEG C of area's temperature, 240~260 DEG C of head temperature, 200~280r/min of screw speed.
The preparation method of any of the above-described PBT composite, includes the following steps:
(1) weigh 60 parts -80 parts PBT, 50 parts of -60 parts of glass fibres, 0.1 part of -0.3 part of SEBS-g-MAH, 2 parts -6 parts Glossiness modified master batch, 0.1 part of -0.3 part of Chimassob, 2020,0.1 parts of -0.5 part of antioxidant;
(2) by the mixture extruding pelletization obtained in step (1) to get to PBT composite.
Double screw extruder in step (2) includes six humidity provinces sequentially arranged, 200~220 DEG C of area's temperature, and two 240~260 DEG C of area's temperature, three 240~260 DEG C of area's temperature, four 240~260 DEG C of area's temperature, five 240~260 DEG C of area's temperature, six 240~260 DEG C of area's temperature, 240~260 DEG C of head temperature, 200~280r/min of screw speed.
Embodiment 1
(1) weigh 60 parts PBT, 50 parts of glass fibres, 0.1 part of SEBS-g-MAH, 2 parts of glossiness modified master batch, 0.1 part 2020,0.1 parts of Irganox1010 of Chimassob;
(2) by the mixture extruding pelletization obtained in step (1) to get to PBT composite P1.
Wherein each area's temperature of double screw extruder and screw speed are respectively;One 200 DEG C of area's temperature, two 240 DEG C of area's temperature, Three 240 DEG C of area's temperature, four 240 DEG C of area's temperature, five 240 DEG C of area's temperature, six 240 DEG C of area's temperature, 240 DEG C of head temperature, screw rod turn Fast 200r/min.
Embodiment 2
(1) weigh 80 parts PBT, 60 parts of glass fibres, 0.3 part of SEBS-g-MAH, 6 parts of glossiness modified master batch, 0.3 part 2020,0.2 parts of Irganox1010 of Chimassob, 0.2 part of Irganox1330,0.1 part of Irganox168;
(2) by the mixture extruding pelletization obtained in step (1) to get to PBT composite P2.
Wherein each area's temperature of double screw extruder and screw speed are respectively;One 220 DEG C of area's temperature, two 260 DEG C of area's temperature, Three 260 DEG C of area's temperature, four 260 DEG C of area's temperature, five 260 DEG C of area's temperature, six 260 DEG C of area's temperature, 260 DEG C of head temperature, screw rod turn Fast 280r/min.
Embodiment 3
(1) weigh 70 parts PBT, 55 parts of glass fibres, 0.2 part of SEBS-g-MAH, 4 parts of glossiness modified master batch, 0.2 part 2020,0.2 parts of Irganox1010 of Chimassob, 0.1 part of Irganox1330;
(2) by the mixture extruding pelletization obtained in step (1) to get to PBT composite P3.
Wherein each area's temperature of double screw extruder and screw speed are respectively;One 210 DEG C of area's temperature, two 250 DEG C of area's temperature, Three 250 DEG C of area's temperature, four 250 DEG C of area's temperature, five 250 DEG C of area's temperature, six 250 DEG C of area's temperature, 250 DEG C of head temperature, screw rod turn Fast 240r/min.
Embodiment 4
(1) weigh 75 parts PBT, 50 parts of glass fibres, 0.3 part of SEBS-g-MAH, 5 parts of glossiness modified master batch, 0.1 part 2020,0.2 parts of Irganox1010 of Chimassob, 0.2 part of Irganox168;
(2) by the mixture extruding pelletization obtained in step (1) to get to PBT composite P4.
Wherein each area's temperature of double screw extruder and screw speed are respectively;One 205 DEG C of area's temperature, two 245 DEG C of area's temperature, Three 245 DEG C of area's temperature, four 245 DEG C of area's temperature, five 245 DEG C of area's temperature, six 245 DEG C of area's temperature, 245 DEG C of head temperature, screw rod turn Fast 230r/min.
Embodiment 5
(1) weigh 65 parts PBT, 54 parts of glass fibres, 0.1 part of SEBS-g-MAH, 3 parts of glossiness modified master batch, 0.3 part 2020,0.3 parts of Irganox1010 of Chimassob, 0.1 part of Irganox1330;
(2) by the mixture extruding pelletization obtained in step (1) to get to PBT composite P5.
Wherein each area's temperature of double screw extruder and screw speed are respectively;One 205 DEG C of area's temperature, two 255 DEG C of area's temperature, Three 255 DEG C of area's temperature, four 255 DEG C of area's temperature, five 255 DEG C of area's temperature, six 255 DEG C of area's temperature, 255 DEG C of head temperature, screw rod turn Fast 245r/min.
Comparative example 1
(1) 70 parts of PBT, 0.3 part of SEBS-g-MAH, 0.1 part of antioxidant 330,0.2 part of antioxidant 264 is weighed to mix and stir It mixes uniformly, obtains mixture;
(2) by the mixture extruding pelletization obtained in step (1) to get to PBT composite D1.
Wherein each area's temperature of double screw extruder and screw speed are respectively;One 205 DEG C of area's temperature, two 255 DEG C of area's temperature, Three 255 DEG C of area's temperature, four 255 DEG C of area's temperature, five 255 DEG C of area's temperature, six 255 DEG C of area's temperature, 255 DEG C of head temperature, screw rod turn Fast 245r/min.
Comparative example 2
(1) weigh 70 parts of PBT, 50 parts of glass fibres, 0.3 part of SEBS-g-MAH, 0.3 part of Irganox1010,0.1 part Irganox1330,0.3 part of Chimassob 2020 are mixed and stirred for uniformly, obtaining mixture;
(2) by the mixture extruding pelletization obtained in step (1) to get to PBT composite D1.
Wherein each area's temperature of double screw extruder and screw speed are respectively;One 205 DEG C of area's temperature, two 255 DEG C of area's temperature, Three 255 DEG C of area's temperature, four 255 DEG C of area's temperature, five 255 DEG C of area's temperature, six 255 DEG C of area's temperature, 255 DEG C of head temperature, screw rod turn Fast 245r/min.
Performance test:
Batten test is made with injection molding machine in PBT composite prepared by above-described embodiment 1-5 and comparative example 1, tests number According to such as following table:
Note:The standard of 1000h degradation references is GB/T1843-2008.
As can be seen from the table, the physical property of embodiment 1-5, weather resistance will be better than comparative example 1.This illustrates this Shen PBT please will be good than the physical property of common PBT composite, weather resistance.
Batten test is made with injection molding machine in PBT composite prepared by above-described embodiment 1-5 and comparative example 2, tests number According to such as following table:
As can be seen from the table, the physical property of embodiment 1-5, weather resistance and comparative example 2 are suitable, but glossiness compared with Good, this illustrates that the PBT of the application is better than the PBT apparent masses of common high glass fiber content.
This has absolutely proved that PBT made from the application has both that physical property, weather resistance are excellent, and apparent mass is good excellent Point, this for extend PBT composite application range.
It although an embodiment of the present invention has been shown and described, for the ordinary skill in the art, can be with Understanding without departing from the principles and spirit of the present invention can carry out these embodiments a variety of variations, modification, replace And deformation, the scope of the present invention are extremely equally limited by appended claims.

Claims (10)

1. a kind of PBT composite, which is characterized in that composed of the following components by weight:
2. PBT composite according to claim 1, which is characterized in that the compatilizer is SEBS-g-MAH.
3. PBT composite according to claim 1, which is characterized in that the glossiness modified master batch, by following weight The component of part is made:
4. PBT composite according to claim 3, which is characterized in that the melting means modifier is mobility modifying agent CBT-100。
5. PBT composite according to claim 3, which is characterized in that the coupling agent is titanate coupling agent AC- 201。
6. PBT composite according to claim 3, which is characterized in that the lubricant is erucyl amide.
7. PBT composite according to claim 3, which is characterized in that the preparation process of the glossiness modified master batch For:
(1) weigh 60 parts of -80 parts of PBT, 10 parts of -16 parts of silicone powders, 16 parts of -20 parts of CBT-100,0.1 part of -0.3 part of AC-201, 0.1 part of -0.5 part of erucyl amide;
(2) by the mixture extruding pelletization obtained in step (1) to get to glossiness modified master batch.
8. PBT composite according to claim 1, which is characterized in that the light stabilizer is Chimassob 2020.
9. PBT composite according to claim 1, which is characterized in that the antioxidant is three (2,4- di-t-butyls) Phenyl-phosphite, four [β-(3,5- di-tert-butyl-hydroxy phenyl) propionic acid] pentaerythritol esters or 1,3,5- trimethyls -2,4,6- The mixing of one or more of (3,5- di-t-butyl -4- hydroxyphenylmethyls) benzene.
10. the preparation method of any one of the claims 1 to 9 PBT composite, which is characterized in that include the following steps:
(1) weigh 60 parts -80 parts PBT, 50 parts of -60 parts of glass fibres, 0.1 part of -0.3 part of SEBS-g-MAH, 2 parts of -6 parts of gloss Spend modified master batch, 0.1 part of -0.3 part of Chimassob, 2020,0.1 parts of -0.5 part of antioxidant;
(2) by the mixture extruding pelletization obtained in step (1) to get to PBT composite.
CN201810638159.4A 2018-06-20 2018-06-20 A kind of PBT composite and preparation method thereof Pending CN108752880A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810638159.4A CN108752880A (en) 2018-06-20 2018-06-20 A kind of PBT composite and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810638159.4A CN108752880A (en) 2018-06-20 2018-06-20 A kind of PBT composite and preparation method thereof

Publications (1)

Publication Number Publication Date
CN108752880A true CN108752880A (en) 2018-11-06

Family

ID=63979498

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810638159.4A Pending CN108752880A (en) 2018-06-20 2018-06-20 A kind of PBT composite and preparation method thereof

Country Status (1)

Country Link
CN (1) CN108752880A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109354840A (en) * 2018-11-12 2019-02-19 任素飞 A kind of PBT composite
CN114163668A (en) * 2021-11-04 2022-03-11 呼和浩特众环工贸股份有限公司 Material of water collecting box of light machine tool and forming method thereof
CN116120678A (en) * 2023-02-27 2023-05-16 吉林化工学院 ABS resin for 3D printing and preparation method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103819829A (en) * 2014-03-16 2014-05-28 贵州省材料产业技术研究院 High-performance engineering plastic/polyester type TPU (thermoplastic polyurethane) alloy material and preparation method thereof
CN104817832A (en) * 2015-05-21 2015-08-05 广东威林工程塑料有限公司 Polybutylene terephthalate composite material
CN107955340A (en) * 2017-11-02 2018-04-24 上海日之升科技有限公司 It is low to distribute automobile air-conditioning air outlet blades PBT material and preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103819829A (en) * 2014-03-16 2014-05-28 贵州省材料产业技术研究院 High-performance engineering plastic/polyester type TPU (thermoplastic polyurethane) alloy material and preparation method thereof
CN104817832A (en) * 2015-05-21 2015-08-05 广东威林工程塑料有限公司 Polybutylene terephthalate composite material
CN107955340A (en) * 2017-11-02 2018-04-24 上海日之升科技有限公司 It is low to distribute automobile air-conditioning air outlet blades PBT material and preparation method thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109354840A (en) * 2018-11-12 2019-02-19 任素飞 A kind of PBT composite
CN114163668A (en) * 2021-11-04 2022-03-11 呼和浩特众环工贸股份有限公司 Material of water collecting box of light machine tool and forming method thereof
CN116120678A (en) * 2023-02-27 2023-05-16 吉林化工学院 ABS resin for 3D printing and preparation method thereof

Similar Documents

Publication Publication Date Title
CN108752880A (en) A kind of PBT composite and preparation method thereof
CN107400343A (en) A kind of fire-retardant scratch-resistant PBT composite and preparation method thereof
CN103421297A (en) Polyphenyl ether / polystyrene blending alloy material and preparation method thereof
CN102040808A (en) Glass fiber enhanced PET/PBT (Polyethylene Terephthalate)/(Polybutylene Terephthalate) alloy with high glossiness and low warping degree and preparation method thereof
CN103131109A (en) Antistatic ultraviolet-resistant ASA/PET alloy material and preparation method thereof
CN101875772B (en) Glass fiber reinforced PC composite material and preparation method thereof
CN109294037A (en) A kind of fire-retardant scratch-resistant high-density polyethylene composite material and preparation method thereof
WO2024125233A2 (en) Polyamide composite material, and preparation method therefor and use thereof
CN108976723A (en) A kind of PBT composite and preparation method thereof
CN109135207A (en) A kind of High Performance Shielding PBT composite and preparation method thereof
CN108690353A (en) A kind of polyphenyl thioether material and preparation method thereof
CN107501776A (en) A kind of delustring high-performance PS composite and preparation method thereof
CN106380713A (en) PC-PS (polycarbonate-polystyrene) composite material and preparation method thereof
CN108752745A (en) A kind of PP composite material and preparation methods of battery pack case
CN109135162A (en) Good ABS composite material of a kind of oil-resistant weather-resistant energy and preparation method thereof
CN107236299A (en) A kind of PA66 AES composite materials and preparation method thereof
CN107266844A (en) A kind of bloom scratch-resistant flame retardant PS composites and preparation method thereof
CN107254133A (en) A kind of fire-retardant AES composite material of high tenacity and preparation method thereof
CN107286656A (en) A kind of PPS composites and preparation method thereof
CN107254165A (en) A kind of PA6 composites and preparation method thereof
CN109777055B (en) Mica powder reinforced montmorillonite modified PBT composite material and preparation method thereof
CN107383743A (en) A kind of AES PMMA composites and preparation method thereof
CN108715674B (en) A kind of PET composite material and preparation method thereof
CN109135277A (en) A kind of PA66 composite material and preparation method
CN109666290A (en) A kind of the PA/AS alloy material and preparation method of the fire-retardant enhancing that has excellent weather resistance

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
CB02 Change of applicant information

Address after: 230601 No. 99 Ziyun Road, Hefei Economic and Technological Development Zone, Anhui Province

Applicant after: Anhui Jianghuai Automobile Group Limited by Share Ltd

Address before: 230601 No. 669 Shixin Road, Taohua Industrial Park, Hefei City, Anhui Province

Applicant before: Anhui Jianghuai Automobile Group Limited by Share Ltd

CB02 Change of applicant information
RJ01 Rejection of invention patent application after publication

Application publication date: 20181106

RJ01 Rejection of invention patent application after publication