CN105504658B - A kind of solvent resistance ABS composite material and preparation method thereof - Google Patents

A kind of solvent resistance ABS composite material and preparation method thereof Download PDF

Info

Publication number
CN105504658B
CN105504658B CN201610007494.5A CN201610007494A CN105504658B CN 105504658 B CN105504658 B CN 105504658B CN 201610007494 A CN201610007494 A CN 201610007494A CN 105504658 B CN105504658 B CN 105504658B
Authority
CN
China
Prior art keywords
parts
temperature
area
solvent resistance
composite material
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.)
Active
Application number
CN201610007494.5A
Other languages
Chinese (zh)
Other versions
CN105504658A (en
Inventor
彭孝茹
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 Jin Gang Industrial Co., Ltd.
Original Assignee
罗仙花
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 罗仙花 filed Critical 罗仙花
Priority to CN201610007494.5A priority Critical patent/CN105504658B/en
Publication of CN105504658A publication Critical patent/CN105504658A/en
Application granted granted Critical
Publication of CN105504658B publication Critical patent/CN105504658B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L55/00Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
    • C08L55/02ABS [Acrylonitrile-Butadiene-Styrene] polymers
    • 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

Abstract

The invention provides a kind of solvent resistance ABS composite material and preparation method thereof.It is prepared by following component:ABS resin, polyimides, 4 third fluorubber, polyvinyl chloride, cumyl peroxide, diethylenetriamines, silane coupler, fatty acid amide, polytetrafluoroethylene (PTFE), dibutyl hydroxy toluene, thio-2 acid double octadecyl, phosphite esters.Its preparation method carries out melting extrusion to feed the mixture into after disperseing 46 minutes under the 15000rpm of rotating speed 13000 in high speed dispersor, extruded product finally is cooled into room temperature, pelletizing produces first to mix all components in double screw extruder.The solvent resistance ABS composite material of the present invention, has extraordinary solvent resistance and crushing resistance, compensate for most of ABS materials not inferior positions of solvent resistance on the market;Its other preparation technology is also relatively simple, is especially suitable for industrialized production.

Description

A kind of solvent resistance ABS composite material and preparation method thereof
Technical field
The present invention relates to Material Field, and in particular to a kind of solvent resistance ABS composite material and preparation method thereof.
Background technology
ABS resin is the thermoplastic polymer formed by three kinds of acrylonitrile, butadiene and styrene monomer copolymerizations, and it is to be situated between A kind of high polymer material between general-purpose plastics and engineering plastics, predominantly granular or pearl, there is nonpoisonous and tasteless, bending resistance Song, high-low temperature resistant, chemicals-resistant, easy processing are molded and the excellent performances such as lustrous surface is good, is widely used in electronics, spins Knit, the industry such as auto industry and building materials.In recent years, with the high performance of electronic apparatus, automobile and light industrial goods etc., people couple The performance of ABS resin proposes further requirement.Wherein, the two big indexs widely used as ABS resin are also simultaneously Two big inferior positions:Not solvent resistance and high breaking property, it is researcher's urgent problem to be solved.
The content of the invention
Technical problems to be solved:It is an object of the invention to provide a kind of solvent resistance ABS composite material, and it is very good to have Solvent resistance and crushing resistance, compensate for most of ABS materials not inferior positions of solvent resistance on the market.
Technical scheme:A kind of solvent resistance ABS composite material, it is prepared by following component with parts by weight:ABS resin 50-70 parts, polyimides 10-20 parts, 4 third fluorubber 10-20 parts, polyvinyl chloride 5-10 parts, cumyl peroxide 1-2 parts, Diethylenetriamines 0.5-1 parts, silane coupler 1-2 parts, fatty acid amide 2-5 parts, polytetrafluoroethylene (PTFE) 1-2 parts, dibutyl hydroxy Toluene 0.2-0.5 parts, the double octadecyl 0.5-1 parts of thio-2 acid, phosphite ester 0.5-1 parts.
It is further preferred that a kind of described solvent resistance ABS composite material, by following component with prepared by parts by weight and Into:ABS resin 55-65 parts, polyimides 13-17 parts, 4 third fluorubber 12-17 parts, polyvinyl chloride 6-9 parts, peroxidating two are different Propyl benzene 1.3-1.8 parts, diethylenetriamines 0.6-0.9 parts, silane coupler 1.3-1.8 parts, fatty acid amide 3-4 parts, polytetrafluoro Ethene 1.3-1.8 parts, dibutyl hydroxy toluene 0.3-0.4 parts, the double octadecyl 0.6-0.9 parts of thio-2 acid, phosphite ester 0.6-0.9 parts.
The preparation method of above-mentioned solvent resistance ABS composite material comprises the following steps:
Step 1:All components are mixed, with scattered 4-6 minutes under rotating speed 13000-15000rpm in high speed dispersor;
Step 2:Feed the mixture into and melting extrusion is carried out in double screw extruder, wherein, the area's temperature of double screw extruder one Spend for 80-100 DEG C, two area's temperature are 150-180 DEG C, and three area's temperature are 200-220 DEG C, and four area's temperature are 190-210 DEG C, 5th area Temperature is 180-210 DEG C, and the residence time is 1-3 minutes, pressure 10-20MPa.
Step 3:Extruded product is cooled to room temperature, pelletizing produces.
It is further preferred that rotating speed is 13500-14500r/min in step 1, jitter time is 4.5-5.5 minutes.
It is further preferred that step 2 Zhong-1 block temperature is 85-95 DEG C, two area's temperature are 160-170 DEG C, and three area's temperature are 205-215 DEG C, four area's temperature are 195-205 DEG C, and five area's temperature are 190-200 DEG C, and the residence time is 1.5-2.5 minutes, pressure For 12-17MPa.
Beneficial effect:Its quality is substantially without change after the solvent resistance ABS composite material of the present invention is soaked one week in acetic acid Change, the mass change of most preferred embodiment only has 0.63%, and outward appearance does not change;Its tensile strength and bending strength are being soaked Also 40MPa and 66MPa or so are still reached after bubble, therefore, one can consider that the present invention's has extraordinary solvent resistance Effect.
Embodiment
Embodiment 1
A kind of solvent resistance ABS composite material, it is prepared by following component with parts by weight:50 parts of ABS resin, polyamides are sub- 10 parts of amine, 10 parts of 4 third fluorubber, 5 parts of polyvinyl chloride, 1 part of cumyl peroxide, 0.5 part of diethylenetriamines, silane are even Join 1 part of agent, 2 parts of fatty acid amide, 1 part of polytetrafluoroethylene (PTFE), 0.2 part of dibutyl hydroxy toluene, the double octadecyls 0.5 of thio-2 acid Part, 0.5 part of phosphite ester.
The preparation method of above-mentioned solvent resistance ABS composite material is:First all components are mixed, in high speed dispersor with Fed the mixture into after disperseing 4 minutes under rotating speed 13000rpm and melting extrusion is carried out in double screw extruder, wherein, twin-screw squeezes The area's temperature of Chu Ji mono- is 80 DEG C, and two area's temperature are 150 DEG C, and three area's temperature are 200 DEG C, and four area's temperature are 190 DEG C, and five area's temperature are 180 DEG C, the residence time is 1 minute, pressure 10MPa, extruded product finally is cooled into room temperature, pelletizing produces.
Embodiment 2
A kind of solvent resistance ABS composite material, it is prepared by following component with parts by weight:60 parts of ABS resin, polyamides are sub- 15 parts of amine, 15 parts of 4 third fluorubber, 7.5 parts of polyvinyl chloride, 1.5 parts of cumyl peroxide, 0.7 part of diethylenetriamines, silicon 1.5 parts of alkane coupling agent, 3.5 parts of fatty acid amide, 1.5 parts of polytetrafluoroethylene (PTFE), 0.3 part of dibutyl hydroxy toluene, thio-2 acid are double 0.7 part of octadecyl, 0.8 part of phosphite ester.
The preparation method of above-mentioned solvent resistance ABS composite material is:First all components are mixed, in high speed dispersor with Fed the mixture into after disperseing 5 minutes under rotating speed 14000rpm and melting extrusion is carried out in double screw extruder, wherein, twin-screw squeezes The area's temperature of Chu Ji mono- is 90 DEG C, and two area's temperature are 165 DEG C, and three area's temperature are 210 DEG C, and four area's temperature are 200 DEG C, and five area's temperature are 195 DEG C, the residence time is 2 minutes, pressure 15MPa, extruded product finally is cooled into room temperature, pelletizing produces.
Embodiment 3
A kind of solvent resistance ABS composite material, it is prepared by following component with parts by weight:70 parts of ABS resin, polyamides are sub- It is 20 parts of amine, 20 parts of 4 third fluorubber, 10 parts of polyvinyl chloride, 2 parts of cumyl peroxide, 1 part of diethylenetriamines, silane coupled 2 parts of agent, 5 parts of fatty acid amide, 2 parts of polytetrafluoroethylene (PTFE), 0.5 part of dibutyl hydroxy toluene, double 1 part of the octadecyl of thio-2 acid, 1 part of phosphite ester.
The preparation method of above-mentioned solvent resistance ABS composite material is:The preparation method of above-mentioned solvent resistance ABS composite material For:First all components are mixed, to feed the mixture into double spiral shells after disperseing 6 minutes under rotating speed 15000rpm in high speed dispersor Melting extrusion is carried out in bar extruder, wherein, the area's temperature of double screw extruder one is 100 DEG C, and two area's temperature are 180 DEG C, 3rd area Temperature is 220 DEG C, and four area's temperature are 210 DEG C, and five area's temperature are 210 DEG C, and the residence time is 3 minutes, pressure 20MPa, finally Extruded product is cooled to room temperature, pelletizing produces.
Embodiment 4
A kind of solvent resistance ABS composite material, it is prepared by following component with parts by weight:55 parts of ABS resin, polyamides are sub- 13 parts of amine, 12 parts of 4 third fluorubber, 6 parts of polyvinyl chloride, 1.3 parts of cumyl peroxide, 0.6 part of diethylenetriamines, silane 1.3 parts of coupling agent, 3 parts of fatty acid amide, 1.3 parts of polytetrafluoroethylene (PTFE), 0.3 part of dibutyl hydroxy toluene, thio-2 acid double 18 0.6 part of alcohol ester, 0.6 part of phosphite ester.
The preparation method of above-mentioned solvent resistance ABS composite material is:The preparation method of above-mentioned solvent resistance ABS composite material For:First all components are mixed, it is double to feed the mixture into after disperseing 4.5 minutes under rotating speed 13500rpm in high speed dispersor Melting extrusion is carried out in screw extruder, wherein, the area's temperature of double screw extruder one is 85 DEG C, and two area's temperature are 160 DEG C, 3rd area Temperature is 205 DEG C, and four area's temperature are 195 DEG C, and five area's temperature are 190 DEG C, and the residence time is 1.5 minutes, pressure 12MPa, most Extruded product is cooled to room temperature afterwards, pelletizing produces.
Embodiment 5
A kind of solvent resistance ABS composite material, it is prepared by following component with parts by weight:65 parts of ABS resin, polyamides are sub- 17 parts of amine, 17 parts of 4 third fluorubber, 9 parts of polyvinyl chloride, 1.8 parts of cumyl peroxide, 0.9 part of diethylenetriamines, silane 1.8 parts of coupling agent, 4 parts of fatty acid amide, 1.8 parts of polytetrafluoroethylene (PTFE), 0.4 part of dibutyl hydroxy toluene, thio-2 acid double 18 0.9 part of alcohol ester, 0.9 part of phosphite ester.
The preparation method of above-mentioned solvent resistance ABS composite material is:The preparation method of above-mentioned solvent resistance ABS composite material For:First all components are mixed, it is double to feed the mixture into after disperseing 5.5 minutes under rotating speed 14500rpm in high speed dispersor Melting extrusion is carried out in screw extruder, wherein, the area's temperature of double screw extruder one is 95 DEG C, and two area's temperature are 170 DEG C, 3rd area Temperature is 215 DEG C, and four area's temperature are 205 DEG C, and five area's temperature are 200 DEG C, and the residence time is 2.5 minutes, pressure 17MPa, most Extruded product is cooled to room temperature afterwards, pelletizing produces.
Comparative example 1
The present embodiment and the difference of embodiment 5 are to replace polyimides with 4 third fluorubber.Specifically:
A kind of solvent resistance ABS composite material, it is prepared by following component with parts by weight:65 parts of ABS resin, 4 third fluorine 34 parts of rubber, 9 parts of polyvinyl chloride, 1.8 parts of cumyl peroxide, 0.9 part of diethylenetriamines, 1.8 parts of silane coupler, fat 4 parts of fat acid amides, 1.8 parts of polytetrafluoroethylene (PTFE), 0.4 part of dibutyl hydroxy toluene, thio-2 acid double 0.9 part of octadecyl, phosphorous 0.9 part of acid esters.
The preparation method of above-mentioned solvent resistance ABS composite material is:The preparation method of above-mentioned solvent resistance ABS composite material For:First all components are mixed, it is double to feed the mixture into after disperseing 5.5 minutes under rotating speed 14500rpm in high speed dispersor Melting extrusion is carried out in screw extruder, wherein, the area's temperature of double screw extruder one is 95 DEG C, and two area's temperature are 170 DEG C, 3rd area Temperature is 215 DEG C, and four area's temperature are 205 DEG C, and five area's temperature are 200 DEG C, and the residence time is 2.5 minutes, pressure 17MPa, most Extruded product is cooled to room temperature afterwards, pelletizing produces.
Comparative example 2
The present embodiment and the difference of embodiment 5 are to replace 4 third fluorubber with polyimides.Specifically:
A kind of solvent resistance ABS composite material, it is prepared by following component with parts by weight:65 parts of ABS resin, polyamides are sub- 34 parts of amine, 9 parts of polyvinyl chloride, 1.8 parts of cumyl peroxide, 0.9 part of diethylenetriamines, 1.8 parts of silane coupler, fat 4 parts of acid amides, 1.8 parts of polytetrafluoroethylene (PTFE), 0.4 part of dibutyl hydroxy toluene, thio-2 acid double 0.9 part of octadecyl, phosphorous acid 0.9 part of ester.
The preparation method of above-mentioned solvent resistance ABS composite material is:The preparation method of above-mentioned solvent resistance ABS composite material For:First all components are mixed, it is double to feed the mixture into after disperseing 5.5 minutes under rotating speed 14500rpm in high speed dispersor Melting extrusion is carried out in screw extruder, wherein, the area's temperature of double screw extruder one is 95 DEG C, and two area's temperature are 170 DEG C, 3rd area Temperature is 215 DEG C, and four area's temperature are 205 DEG C, and five area's temperature are 200 DEG C, and the residence time is 2.5 minutes, pressure 17MPa, most Extruded product is cooled to room temperature afterwards, pelletizing produces.
Each embodiment is compared with comparative example, comparing result such as table 1 below:
The performance indications of the solvent resistance ABS composite material of table 1
Name of product Mass change(%) Cosmetic variation grade Tensile strength (MPa) Bending strength(MPa)
Embodiment 1 0.81 It is unchanged 39.87 65.1
Embodiment 2 0.72 It is unchanged 40.32 65.5
Embodiment 3 0.68 It is unchanged 40.91 65.8
Embodiment 4 0.74 It is unchanged 39.93 65.3
Embodiment 5 0.63 It is unchanged 41.69 66.2
Comparative example 1 1.18 Unobvious change 36.12 51.3
Comparative example 2 1.32 Unobvious change 35.37 50.2
Note:Mass change and appearance ratings change turn to 5% acetic acid of immersion and determined after 1 week
As known from Table 1, its quality is substantially unchanged after embodiment 1-5 soaks one week in acetic acid, the matter of most preferred embodiment 5 Quantitative change rate only has 0.63%, and outward appearance does not change;Its tensile strength and bending strength also still reach after steeping 40MPa and 66MPa or so, therefore, one can consider that the solvent resistance of the present invention is very good.Compared with comparative example, find The indices of comparative example 1 and 2 are all deteriorated, and comparative example 2 is particularly evident, illustrate by after polyimides and 4 third fluorubber compounding The one kind wherein appointed significantly larger than is used alone to the effect of the solvent resistance of the present invention.

Claims (5)

  1. A kind of 1. solvent resistance ABS composite material, it is characterised in that:It is prepared by following component with parts by weight:ABS resin 50-70 parts, polyimides 10-20 parts, 4 third fluorubber 10-20 parts, polyvinyl chloride 5-10 parts, cumyl peroxide 1-2 parts, Diethylenetriamines 0.5-1 parts, silane coupler 1-2 parts, fatty acid amide 2-5 parts, polytetrafluoroethylene (PTFE) 1-2 parts, dibutyl hydroxy Toluene 0.2-0.5 parts, the double octadecyl 0.5-1 parts of thio-2 acid, phosphite ester 0.5-1 parts.
  2. A kind of 2. solvent resistance ABS composite material according to claim 1, it is characterised in that:By following component with weight Part is prepared:ABS resin 55-65 parts, polyimides 13-17 parts, 4 third fluorubber 12-17 parts, polyvinyl chloride 6-9 parts, mistake Aoxidize diisopropylbenzene (DIPB) 1.3-1.8 parts, diethylenetriamines 0.6-0.9 parts, silane coupler 1.3-1.8 parts, fatty acid amide 3-4 Part, polytetrafluoroethylene (PTFE) 1.3-1.8 parts, dibutyl hydroxy toluene 0.3-0.4 parts, the double octadecyl 0.6-0.9 parts of thio-2 acid, Phosphite ester 0.6-0.9 parts.
  3. A kind of 3. preparation method of solvent resistance ABS composite material described in any one of claim 1 to 2, it is characterised in that:Bag Include following steps:
    Step 1:All components are mixed, with scattered 4-6 minutes under rotating speed 13000-15000rpm in high speed dispersor;
    Step 2:Feed the mixture into and melting extrusion is carried out in double screw extruder, wherein, the area's temperature of double screw extruder one is 80-100 DEG C, two area's temperature are 150-180 DEG C, and three area's temperature are 200-220 DEG C, and four area's temperature are 190-210 DEG C, five area's temperature For 180-210 DEG C, the residence time is 1-3 minutes, pressure 10-20MPa;
    Step 3:Extruded product is cooled to room temperature, pelletizing produces.
  4. A kind of 4. preparation method of solvent resistance ABS composite material according to claim 3, it is characterised in that:The step Rotating speed is 13500-14500r/min in rapid 1, and jitter time is 4.5-5.5 minutes.
  5. A kind of 5. preparation method of solvent resistance ABS composite material according to claim 3, it is characterised in that:The step Rapid 2 Zhong-1 block temperature is 85-95 DEG C, and two area's temperature are 160-170 DEG C, and three area's temperature are 205-215 DEG C, and four area's temperature are 195- 205 DEG C, five area's temperature are 190-200 DEG C, and the residence time is 1.5-2.5 minutes, pressure 12-17MPa.
CN201610007494.5A 2016-01-07 2016-01-07 A kind of solvent resistance ABS composite material and preparation method thereof Active CN105504658B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610007494.5A CN105504658B (en) 2016-01-07 2016-01-07 A kind of solvent resistance ABS composite material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610007494.5A CN105504658B (en) 2016-01-07 2016-01-07 A kind of solvent resistance ABS composite material and preparation method thereof

Publications (2)

Publication Number Publication Date
CN105504658A CN105504658A (en) 2016-04-20
CN105504658B true CN105504658B (en) 2017-11-14

Family

ID=55712983

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610007494.5A Active CN105504658B (en) 2016-01-07 2016-01-07 A kind of solvent resistance ABS composite material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN105504658B (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0509459A1 (en) * 1991-04-15 1992-10-21 Nippon Shokubai Co., Ltd. Maleimide-based copolymer,process for producing it, and thermoplastic resin composition containing the same
CN102477206A (en) * 2010-11-29 2012-05-30 合肥杰事杰新材料股份有限公司 Flame retardant and antistatic ABS/PVC alloy material, and preparation method thereof
CN102675816A (en) * 2012-05-22 2012-09-19 苏州新区华士达工程塑胶有限公司 Formula of heat-resistant ABS (acrylonitrile-butadiene-styrene)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102585330A (en) * 2012-01-18 2012-07-18 厦门虹鹭钨钼工业有限公司 Tungsten-polymer composite material and preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0509459A1 (en) * 1991-04-15 1992-10-21 Nippon Shokubai Co., Ltd. Maleimide-based copolymer,process for producing it, and thermoplastic resin composition containing the same
CN102477206A (en) * 2010-11-29 2012-05-30 合肥杰事杰新材料股份有限公司 Flame retardant and antistatic ABS/PVC alloy material, and preparation method thereof
CN102675816A (en) * 2012-05-22 2012-09-19 苏州新区华士达工程塑胶有限公司 Formula of heat-resistant ABS (acrylonitrile-butadiene-styrene)

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
"ABS复合材料耐溶剂的研究";郭建兵 等;《塑料》;20080531;第37卷(第5期);第80-82页 *

Also Published As

Publication number Publication date
CN105504658A (en) 2016-04-20

Similar Documents

Publication Publication Date Title
CN107501928B (en) Hydrolysis-resistant nylon material and preparation method thereof
CN105440438B (en) A kind of high PASS PP composite material and preparation method thereof
CN104086969B (en) A kind of transparent scrape resistant PC/PMMA alloy material and preparation method thereof
JP6821475B2 (en) Method for producing modified cellulose nanofibers
CN106317547B (en) Ultrahigh molecular weight polyethylene composition for extrusion molding and preparation method thereof
US20080293861A1 (en) Composition of high impact glass fiber reinforced engineering plastic and preparation method thereof
CN103589069A (en) High-shock resistance polypropylene/polybutylene composite material as well as preparation method and purposes thereof
CN110092954B (en) Nitrile rubber/nylon thermoplastic elastomer and preparation method thereof
CN104334630A (en) Crosslinked polyethylene composition having improved processability
CN102863785A (en) Enhanced polyamide compound and preparation method thereof
CN103289370A (en) Modified elastomer of nylon 6 and preparation method thereof
CN104672507A (en) Thermoplastic starch capable of being subjected to repeated hot-processing and preparation method of thermoplastic starch
CN110698851B (en) High-toughness spraying-free polyamide 11 material and preparation method thereof
CN102304252B (en) Thermoplastic polyolefin elastomer, and preparation method and application thereof
CN105504658B (en) A kind of solvent resistance ABS composite material and preparation method thereof
CN102532718A (en) Permanent antistatic polypropylene material and preparation method thereof
CN104927248B (en) Sole of outdoor shoe modified PVC resin material
CN107523048B (en) Wear-resistant nylon material and preparation method thereof
CN107541004B (en) Load-resistant and fatigue-resistant TPE (thermoplastic elastomer) and preparation method thereof
CN104086940A (en) Halogen-free flame retardant TPE (thermoplastic polyurethane elastomer) injection molding material and preparation method thereof
CN110734630A (en) high-toughness PET material for plastic uptake box
CN111040307A (en) Polypropylene corrugated pipe composite material and preparation method of composite polypropylene corrugated pipe
CN104411763A (en) Crosslinked polyethylene composition
CN105061949A (en) Insulating PVC (polyvinyl chloride) plastic particle
CN111675898B (en) Low-water-absorption toughened polyamide material and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
TA01 Transfer of patent application right

Effective date of registration: 20170927

Address after: 318050 Zhejiang Province, Luqiao District, the new town of the former village of the first seven Wu District No. 3, No. 24, No.

Applicant after: Luo Xianhua

Address before: 215000 Suzhou high tech Zone, Jiangsu Province Road, No. 287

Applicant before: SUZHOU FASITE INFORMATION TECHNOLOGY CO., LTD.

TA01 Transfer of patent application right
GR01 Patent grant
GR01 Patent grant
CB03 Change of inventor or designer information

Inventor after: Lin Xuewu

Inventor before: Peng Xiaoru

CB03 Change of inventor or designer information
TR01 Transfer of patent right

Effective date of registration: 20180108

Address after: 515100 Sima Pu Xian Port Road in Chaonan District, Shantou, Guangdong

Patentee after: Guangdong Jin Gang Industrial Co., Ltd.

Address before: 318050 Zhejiang Province, Luqiao District, the new town of the former village of the first seven Wu District No. 3, No. 24, No.

Patentee before: Luo Xianhua

TR01 Transfer of patent right