CN106700253B - A kind of low-contraction low-density PP material and preparation method thereof - Google Patents

A kind of low-contraction low-density PP material and preparation method thereof Download PDF

Info

Publication number
CN106700253B
CN106700253B CN201611153457.1A CN201611153457A CN106700253B CN 106700253 B CN106700253 B CN 106700253B CN 201611153457 A CN201611153457 A CN 201611153457A CN 106700253 B CN106700253 B CN 106700253B
Authority
CN
China
Prior art keywords
low
density
contraction
parts
epoxy resin
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.)
Withdrawn - After Issue
Application number
CN201611153457.1A
Other languages
Chinese (zh)
Other versions
CN106700253A (en
Inventor
王灿耀
于海鸥
易庆锋
桑杰
杨贵昌
方安平
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 Harmony New Materials Co Ltd
Original Assignee
Guangdong Harmony New Materials Co Ltd
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 Guangdong Harmony New Materials Co Ltd filed Critical Guangdong Harmony New Materials Co Ltd
Priority to CN201611153457.1A priority Critical patent/CN106700253B/en
Publication of CN106700253A publication Critical patent/CN106700253A/en
Application granted granted Critical
Publication of CN106700253B publication Critical patent/CN106700253B/en
Withdrawn - After Issue legal-status Critical Current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
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/12Polypropene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B9/00Making granules
    • B29B9/02Making granules by dividing preformed material
    • B29B9/06Making granules by dividing preformed material in the form of filamentary material, e.g. combined with extrusion
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/022Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the choice of material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/04Particle-shaped
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/36Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die
    • B29C48/50Details of extruders
    • B29C48/505Screws
    • B29C48/67Screws having incorporated mixing devices not provided for in groups B29C48/52 - B29C48/66
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/14Copolymers of propene
    • 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2312/00Crosslinking

Abstract

The invention belongs to modified material technical fields, disclose a kind of low-contraction low-density PP material, according to parts by weight, including following components: 85 ~ 95 parts of acrylic resin, 1 ~ 5 part of polyolefin elastomer, 3 ~ 8 parts of rigid molecule chain material, 1 ~ 5 part of epoxy resin, 0.1 ~ 0.5 part of crosslinking agent, 0.1 ~ 0.5 part of cross-linking aid, 0.2 ~ 0.4 part of antioxidant, 0.2 ~ 0.4 part of weather resisting agent.The invention also discloses the preparation methods of the PP material.The material that the present invention need to only add minimal amount of big steric hindrance functional group rigid molecular segments can reach 0.7 ~ 0.9% low molding shrinkage, while influence on the strong and unyielding property of PP material slighter;Low (the < 0.93g/cm of density of material prepared by the present invention3), meet the needs of lightweight trend;And improve the scratch resistant performance of PP material.

Description

A kind of low-contraction low-density PP material and preparation method thereof
Technical field
The invention belongs to modified material technical fields, and in particular to a kind of low-contraction low-density PP material and its preparation side Method.
Background technique
PP is one of five big general-purpose plastics, and density is low, is widely used in the fields such as automobile, household electrical appliances, toy.However, PP has One maximum weakness is that molding shrinkage is big, this brings certain puzzlement to die sinking and molded article dimensional stability.At present There are two ways to the most frequently used reduction PP shrinking percentage: it one is addition is mineral-filled, is reduced with the spatial position benefit of mineral Material shrinkage.The method significant effect, but the density of material is increased, destroy the excellent of the low-density that PP material itself has Gesture;The second is adding another high molecular material by the way of alloy, the structural integrity of PP material is destroyed, reduces material knot Crystalline substance reduces material shrinkage, and it is just effective that the method needs to add larger amount of alloy compositions, will affect the machinery of PP material Performance.
The patent document of Publication No. CN201511018344 discloses a kind of by addition mineral filler and olefin-modified Agent synergistic prepares a kind of specific gravity down to 0.97g/cm3, the lower shrinkage low-gravity polypropylene material that shrinking percentage is 0.6~0.8%. The patent document of Publication No. CN201310432874 discloses a kind of shrinking percentage that PP is reduced by way of PP/ABS alloy. The patent document of Publication No. CN200810030391, which discloses, a kind of prepares molding shrinkage by way of PP/PS alloy For 0.7~0.9% PP material, close to the level of ABS.The patent document of Publication No. CN201210124421 discloses one kind The mode of In Situ Compatibilization reactive extrursion prepares lower molding shrinkage PO/PS alloy material.
However, current low-density lower shrinkage PP density generally accomplishes 0.97g/cm3 or more, compared to PP resin The density of 0.9g/cm3, there is also a certain distance.
Summary of the invention
In view of the deficiencies of the prior art, it is an object of the present invention to provide a kind of PP material, neither damage PP material is original Low-density advantage, and the PP mechanical property of materials is less influenced, while reaching the low requirement of molding shrinkage.
It is a further object of the present invention to provide the preparation methods of the PP material.
One of in order to achieve the above objectives, the invention adopts the following technical scheme:
A kind of low-contraction low-density PP material, according to parts by weight, including following components:
85~95 parts of acrylic resin
1~5 part of polyolefin elastomer
3~8 parts of rigid molecule chain material
1~5 part of epoxy resin
0.1~0.5 part of crosslinking agent
0.1~0.5 part of cross-linking aid
0.2~0.4 part of antioxidant
0.2~0.4 part of weather resisting agent.
Further, the acrylic resin is selected from one of homopolymerization or copolymer polypropylene or two kinds of mixing Object, melt index under the conditions of 230 DEG C/2.16kg are 1~100g/10min.
Further, the polyolefin elastomer is selected from ethylene-butene copolymer, ethylene-octene copolymer, ethylene-the third At least one of alkene-diene copolymer;Optimal ethylene-octene copolymer, 1~15g/10min of melt index (ISO 1133,230 DEG C/2.16kg), octene content is greater than 25%.
Further, the rigid molecule chain material is selected from polystyrene, polymethyl methacrylate, styrene-propene At least one of lonitrile copolymer;It is preferred that polymethyl methacrylate.
Further, the epoxy resin is selected from bisphenol A type epoxy resin, glycidyl ether type epoxy resin, organic titanium Epoxy resin or cycloaliphatic epoxy resin;It is preferred that cycloaliphatic epoxy resin.
Further, the crosslinking agent is selected from cumyl peroxide, Isosorbide-5-Nitrae-dual-tert-butyl peroxy isopropyl base benzene, peroxidating At least one of benzoyl, 2,5- dimethyl -2,5 two (t-butylperoxy) hexane;It is preferred that 1,4- dual-tert-butyl peroxide is different Propylbenzene.
Further, the cross-linking aid is selected from polybutadiene and/or trimethylolpropane trimethacrylate, molecular weight < 6000。
Further, the antioxidant is selected from Hinered phenols antioxidant 1010 and/or phosphite ester antioxidant 168.
Further, the weather resisting agent is selected from hindered amine light stabilizer UV-3808PP5.
A method of low-contraction low-density PP material described in any one of claim 1 to 9 being prepared, specifically: will Raw material is put into batch mixer and is uniformly mixed, and is then placed in double screw extruder extruding pelletization, and melt zone is pinched using three sections, 90 ° of rotation angles Close element and a section small lead delivery element block installation, 350~450r/min of engine speed, extrusion process temperature is 180~ 200℃。
Compared with prior art, the present invention is by adding a small amount of rigid molecule chain material, with crosslinking agent initiation grafting, It reduces the structural integrity of PP material and reduces the crystallization of material, along with the grafting booster action of epoxy resin improves grafting Efficiency, while the space steric effect of epoxy resin itself make mutually to wind between strand, to reach the effect of lower shrinkage Fruit.So the present invention has following advantage:
1, it is wanted compared to PP alloy material although simple material blending method can also reduce the shrinking percentage of material Reach lower shrinking percentage effect, non-PP ingredient needs to add that number is more, seriously affects the mechanical performance of PP material.The present invention The material that minimal amount of big steric hindrance functional group rigid molecular segments need to only be added can reach 0.7~0.9% low inprocess shrinkage Therefore rate while material prepared by the present invention reduces material molding shrinkage, influences the strong and unyielding property of PP material slighter.
2, compared to mineral-filled PP material, under the premise of reaching identical molding shrinkage, material prepared by the present invention Expect density it is low (< 0.93g/cm3), meet the needs of lightweight trend, can directly substitute the mineral-filled PP material of high density without With more mold exchange, it also can be made master batch for automobile/family's electric material and make shrinking percentage regulator.
3, by the addition of rigid particles and epoxy resin, the surface hardness of material is improved, improves the resistance to of PP material Scratch performance.
4, the present invention uses special process screw combinations, and melt zone is small using three sections, 90 ° of rotation angle kneading members and a section The installation of lead delivery element block, has the strong dispersibility of low-heat-generation, avoids material from hot-spot occur and influence to be grafted.
Specific embodiment
The present invention is described further combined with specific embodiments below.
In following embodiment, acrylic resin used is selected from the mixed of one of homopolymerization or copolymer polypropylene or two kinds Object is closed, melt index under the conditions of 230 DEG C/2.16kg is 1~100g/10min.Crosslinking agent used is selected from peroxidating diisopropyl Benzene, 1,4 bis tert butyl peroxy isopropyl benzene, benzoyl peroxide, in 2,5- dimethyl -2,5 two (t-butylperoxy) hexane At least one.Cross-linking aid used is selected from polybutadiene and/or trimethylolpropane trimethacrylate, molecular weight < 6000. Antioxidant used is selected from Hinered phenols antioxidant 1010 and/or phosphite ester antioxidant 168.Weather resisting agent used is selected from hindered amine Class light stabilizer UV-3808PP5.It is purchased from commercially produced product.
Embodiment 1
A kind of low-contraction low-density polypropylene material, is made of the raw material of following parts by weight:
85 parts of acrylic resin
5 parts of ethylene-octene copolymer
8 parts of polymethyl methacrylate
2 parts of bisphenol A type epoxy resin
0.2 part of crosslinking agent
0.2 part of cross-linking aid
0.4 part of antioxidant
0.2 part of weather resisting agent
By acrylic resin, ethylene-octene copolymer, polymethyl methacrylate, bisphenol A type epoxy resin, crosslinking agent, Cross-linking aid, antioxidant, weather resisting agent are put into batch mixer and are uniformly mixed (3 minutes), are then placed in double screw extruder extruding pelletization, Using three sections, 90 ° of rotation angle kneading members and the small lead delivery element block installation of a section, which has low melt zone The strong dispersibility of heat, avoids material from hot-spot occur and influences to be grafted, 350~450r/min of engine speed, extrusion process Temperature is 180~200 DEG C.Its performance parameter is as shown in table 1.
Embodiment 2
A kind of low-contraction low-density polypropylene material, is made of the raw material of following parts by weight:
85 parts of acrylic resin
2 parts of ethylene-octene copolymer
8 parts of polymethyl methacrylate
5 parts of bisphenol A type epoxy resin
0.2 part of crosslinking agent
0.2 part of cross-linking aid
0.4 part of antioxidant
0.2 part of weather resisting agent
For its preparation process with example 1, performance parameter is as shown in table 1.
Embodiment 3
A kind of low-contraction low-density polypropylene material, is made of the raw material of following parts by weight:
95 parts of acrylic resin
5 parts of ethylene-octene copolymer
5 parts of polymethyl methacrylate
5 parts of bisphenol A type epoxy resin
0.5 part of crosslinking agent
0.5 part of cross-linking aid
0.4 part of antioxidant
0.2 part of weather resisting agent
For its preparation process with example 1, performance parameter is as shown in table 1.
Embodiment 4
A kind of low-contraction low-density polypropylene material, is made of the raw material of following parts by weight:
87 parts of acrylic resin
1 part of ethylene-butene copolymer
3 parts of polystyrene
1 part of glycerol epoxy resin
0.1 part of crosslinking agent
0.1 part of cross-linking aid
0.2 part of antioxidant
0.4 part of weather resisting agent
Its preparation process is the same as example 1.
Embodiment 5
A kind of low-contraction low-density polypropylene material, is made of the raw material of following parts by weight:
92 parts of acrylic resin
3 parts of ethylene-propylene-diene copolymer
8 parts of styrene-acrylonitrile copolymer
2 parts of organotitanium epoxy resin
0.3 part of crosslinking agent
0.3 part of cross-linking aid
0.3 part of antioxidant
0.3 part of weather resisting agent
Its preparation process is the same as example 1.
Embodiment 6
A kind of low-contraction low-density polypropylene material, is made of the raw material of following parts by weight:
90 parts of acrylic resin
4 parts of ethylene-propylene-diene copolymer
6 parts of polystyrene
4 parts of cycloaliphatic epoxy resin
0.4 part of crosslinking agent
0.4 part of cross-linking aid
0.3 part of antioxidant
0.3 part of weather resisting agent
Its preparation process is the same as example 1.
Comparative example 1
A kind of polypropylene material is made of the raw material of following parts by weight:
90 parts of acrylic resin
0.4 part of antioxidant
0.2 part of weather resisting agent
For its preparation process with example 1, performance parameter is as shown in table 1.
Comparative example 2
A kind of polypropylene alloy material is made of the raw material of following parts by weight:
90 parts of acrylic resin
5 parts of ethylene-octene copolymer
5 parts of polymethyl methacrylate
0.4 part of antioxidant
0.2 part of weather resisting agent
For its preparation process with example 1, performance parameter is as shown in table 1.
Comparative example 3
A kind of polypropylene alloy material is made of the raw material of following parts by weight:
85 parts of acrylic resin
5 parts of ethylene-octene copolymer
5 parts of polymethyl methacrylate
5 parts of bisphenol A type epoxy resin
0.4 part of antioxidant
0.2 part of weather resisting agent
For its preparation process with example 1, performance parameter is as shown in table 1.
Comparative example 4
A kind of polypropylene alloy material is made of the raw material of following parts by weight:
90 parts of acrylic resin
5 parts of ethylene-octene copolymer
5 parts of polymethyl methacrylate
0.5 part of crosslinking agent
0.5 part of cross-linking aid
0.4 part of antioxidant
0.2 part of weather resisting agent
For its preparation process with example 1, performance parameter is as shown in table 1.
Comparative example 5
A kind of polypropylene alloy material is made of the raw material of following parts by weight:
85 parts of acrylic resin
5 parts of ethylene-octene copolymer
5 parts of polymethyl methacrylate
5 parts of bisphenol A type epoxy resin
0.5 part of crosslinking agent
0.5 part of cross-linking aid
0.4 part of antioxidant
0.2 part of weather resisting agent
Acrylic resin, ethylene-octene copolymer, polymethyl methacrylate, epoxy resin, crosslinking agent, crosslinking are helped Agent, antioxidant, weather resisting agent are put into batch mixer and are uniformly mixed (3 minutes), are then placed in double screw extruder extruding pelletization, technique spiral shell High heat strong dispersibility design of the bar combination by common PP material, 350~450r/min of engine speed, extrusion process temperature are 180~200 DEG C.Its performance parameter is as shown in table 1.
Performance test
The above-mentioned material prepared is put into injection molding machine and beats mechanics batten, colour table and shrinking percentage plate, the mould of shrinking percentage plate Tool specification is thickness 2.0mm, length 150mm, width 15mm, and mechanics batten and colour table Shooting Technique are 200 DEG C of temperature, injection molding pressure Power 45bar, firing rate 45mm/s, pressure maintaining 15sec, shrinking percentage plate Shooting Technique are 200 DEG C of temperature, injection pressure 45bar, firing rate 45mm/s, pressure maintaining 5sec.Each case presses ISO testing standard, and the physical property measured, shrinking percentage, cross scraping color difference result are as follows:
The performance parameter of the component proportion and product of 1 various embodiments of the present invention of table and comparative example
By table 1 it follows that
1, it can be seen that by comparative example 2, comparative example 3, Examples 1 to 6 and be blended compared to General Physics, chemical graft Mode significantly reduce the molding shrinkage of material, especially have the synergistic effect of epoxy resin, the inprocess shrinkage of material Rate has apparent reduction.
2, by comparative example 1~4, Examples 1 to 6 it can be concluded that, pass through chemical graft rigid particles synergistic epoxy resin The material of method preparation both had that molding shrinkage is low, but also with the low-density close to PP material, while to the object of PP material Property influence it is little.After introducing Grafted rigid particle, the scratch resistant performance of material is obviously improved.
3, by comparative example 5 and Examples 1 to 6 it can be concluded that, the design of new screw group technology improves connecing for material Branch efficiency, improves the compatibility of material, while reducing material molding shrinkage, improves the impact property of material.
The above description is merely a specific embodiment, but scope of protection of the present invention is not limited thereto, any Belong to those skilled in the art in the technical scope disclosed by the present invention, any changes or substitutions that can be easily thought of, all answers It is included within the scope of the present invention.Therefore, protection scope of the present invention should be subject to the protection scope in claims.

Claims (10)

1. a kind of low-contraction low-density PP material, which is characterized in that according to parts by weight, including following components:
2. low-contraction low-density PP material according to claim 1, which is characterized in that the acrylic resin is selected from homopolymerization Either one of copolymer polypropylene or two kinds of mixture, melt index under the conditions of 230 DEG C/2.16kg is 1~ 100g/10min。
3. low-contraction low-density PP material according to claim 1, which is characterized in that the polyolefin elastomer is selected from second At least one of alkene-butylene copolymer, ethylene-octene copolymer, ethylene-propylene-diene copolymer.
4. low-contraction low-density PP material according to claim 1, which is characterized in that the rigid molecule chain material is selected from At least one of polystyrene, polymethyl methacrylate, styrene-acrylonitrile copolymer.
5. low-contraction low-density PP material according to claim 1, which is characterized in that the epoxy resin is selected from bisphenol-A Type epoxy resin, glycidyl ether type epoxy resin, organotitanium epoxy resin or cycloaliphatic epoxy resin.
6. low-contraction low-density PP material according to claim 1, which is characterized in that the crosslinking agent is selected from peroxidating two Isopropylbenzene, 1,4 bis tert butyl peroxy isopropyl benzene, benzoyl peroxide, 2,5- dimethyl -2,5 two (t-butylperoxy) oneself At least one of alkane.
7. low-contraction low-density PP material according to claim 1, which is characterized in that the cross-linking aid is selected from polybutadiene Alkene and/or trimethylolpropane trimethacrylate, molecular weight < 6000.
8. low-contraction low-density PP material according to claim 1, which is characterized in that the antioxidant is selected from Hinered phenols Antioxidant 1010 and/or phosphite ester antioxidant 168.
9. low-contraction low-density PP material according to claim 1, which is characterized in that the weather resisting agent is selected from hindered amines Light stabilizer UV-3808PP5.
10. a kind of method for preparing low-contraction low-density PP material described in any one of claim 1 to 9, which is characterized in that Raw material is put into batch mixer to be uniformly mixed, is then placed in double screw extruder extruding pelletization, melt zone uses three sections, 90 ° of rotation angles Kneading member and the small lead delivery element block installation of a section, 350~450r/min of engine speed, extrusion process temperature is 180 ~200 DEG C.
CN201611153457.1A 2016-12-14 2016-12-14 A kind of low-contraction low-density PP material and preparation method thereof Withdrawn - After Issue CN106700253B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201611153457.1A CN106700253B (en) 2016-12-14 2016-12-14 A kind of low-contraction low-density PP material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201611153457.1A CN106700253B (en) 2016-12-14 2016-12-14 A kind of low-contraction low-density PP material and preparation method thereof

Publications (2)

Publication Number Publication Date
CN106700253A CN106700253A (en) 2017-05-24
CN106700253B true CN106700253B (en) 2019-03-01

Family

ID=58936905

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201611153457.1A Withdrawn - After Issue CN106700253B (en) 2016-12-14 2016-12-14 A kind of low-contraction low-density PP material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN106700253B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE202018101394U1 (en) * 2018-03-13 2019-06-14 Rehau Ag + Co Polymer composition for a 3D printing process
CN112778634A (en) * 2020-12-29 2021-05-11 成都金发科技新材料有限公司 Rigid-tough balance low-density polypropylene composite material and preparation method and application thereof
CN112852057A (en) * 2021-01-19 2021-05-28 安特普工程塑料(苏州)有限公司 Anti-aging improved polypropylene composition and preparation method thereof

Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3766135A (en) * 1970-04-16 1973-10-16 Sumitomo Chemical Co Reinforced polypropylene composition and its production
JP2008231129A (en) * 2007-03-16 2008-10-02 Toyo Ink Mfg Co Ltd Resin composition and molded article
CN101338063A (en) * 2008-03-31 2009-01-07 东莞金富亮塑胶颜料有限公司 Polypropylene (PP) alloy
CN201520053U (en) * 2009-09-25 2010-07-07 重庆嘉良塑胶制品有限责任公司 Combined screw for twin-screw extruder
CN101993564A (en) * 2009-08-24 2011-03-30 新疆大学 Method for preparing polypropylene material special for automobile instrument panel
CN102286168A (en) * 2011-06-30 2011-12-21 国家复合改性聚合物材料工程技术研究中心 Polypropylene/ acrylonitrile styrene (AS) blend and preparation method thereof and thermal treatment method for product
CN102643484A (en) * 2012-04-25 2012-08-22 金发科技股份有限公司 In-situ compatibilization polyolefin/polystyrene alloy and preparation method and application thereof
CN103289188A (en) * 2013-02-25 2013-09-11 金发科技股份有限公司 Polypropylene compound, its preparation method and application
CN103819817A (en) * 2014-03-11 2014-05-28 株洲时代新材料科技股份有限公司 Polypropylene composition with high fluidity and high dimensional stability and preparation method thereof
CN104592645A (en) * 2014-12-22 2015-05-06 上海普利特复合材料股份有限公司 Low-density low-shrinkage high-impact polypropylene composite material and preparation method thereof
CN105524354A (en) * 2015-12-30 2016-04-27 宁波科普特新材料有限公司 A low-shrinkage low-specific-gravity PP material and a preparing method thereof
CN105647004A (en) * 2014-11-14 2016-06-08 王洪珠 Environmentally-friendly modified car bumper

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3766135A (en) * 1970-04-16 1973-10-16 Sumitomo Chemical Co Reinforced polypropylene composition and its production
JP2008231129A (en) * 2007-03-16 2008-10-02 Toyo Ink Mfg Co Ltd Resin composition and molded article
CN101338063A (en) * 2008-03-31 2009-01-07 东莞金富亮塑胶颜料有限公司 Polypropylene (PP) alloy
CN101993564A (en) * 2009-08-24 2011-03-30 新疆大学 Method for preparing polypropylene material special for automobile instrument panel
CN201520053U (en) * 2009-09-25 2010-07-07 重庆嘉良塑胶制品有限责任公司 Combined screw for twin-screw extruder
CN102286168A (en) * 2011-06-30 2011-12-21 国家复合改性聚合物材料工程技术研究中心 Polypropylene/ acrylonitrile styrene (AS) blend and preparation method thereof and thermal treatment method for product
CN102643484A (en) * 2012-04-25 2012-08-22 金发科技股份有限公司 In-situ compatibilization polyolefin/polystyrene alloy and preparation method and application thereof
CN103289188A (en) * 2013-02-25 2013-09-11 金发科技股份有限公司 Polypropylene compound, its preparation method and application
CN103819817A (en) * 2014-03-11 2014-05-28 株洲时代新材料科技股份有限公司 Polypropylene composition with high fluidity and high dimensional stability and preparation method thereof
CN105647004A (en) * 2014-11-14 2016-06-08 王洪珠 Environmentally-friendly modified car bumper
CN104592645A (en) * 2014-12-22 2015-05-06 上海普利特复合材料股份有限公司 Low-density low-shrinkage high-impact polypropylene composite material and preparation method thereof
CN105524354A (en) * 2015-12-30 2016-04-27 宁波科普特新材料有限公司 A low-shrinkage low-specific-gravity PP material and a preparing method thereof

Also Published As

Publication number Publication date
CN106700253A (en) 2017-05-24

Similar Documents

Publication Publication Date Title
CN107722448B (en) Composite composition for automotive interior material using natural fiber
CN106046589B (en) A kind of thermoplastic abs resin composition for the high rigidity of blow molding, high fondant-strength and low-temperature impact resistance
CN106700253B (en) A kind of low-contraction low-density PP material and preparation method thereof
CN103756240B (en) A kind of proof stress turns white ABS composite material and its preparation method and application
CN103980672A (en) 3D printing aromatic polyester material and preparation method thereof
CN107434913B (en) Halogen-free flame-retardant anti-UV strong-bonding PA encapsulating material and preparation method thereof
CN105820522A (en) Calcium sulfate whisker reinforced and toughened polylactic acid composite and preparation method thereof
CN110452549A (en) Thermoplastic elastomer (TPE)-silicone resin composite material and preparation method thereof
CN107383615A (en) A kind of modified polypropylene material and preparation method thereof
CN103436012B (en) Ultrahigh-molecular weight polyethylene modified nylon 66 and preparation method thereof
CN104194123B (en) The preparation method of polyacrylonitrile fibre/high-density polyethylene composite material
CN104725844A (en) Micro-foaming PA/ASA (polyamide/acrylonitrile styrene acrylate) material and preparation method thereof
CN112029258A (en) Environment-friendly reinforced PC (polycarbonate) and ABS (acrylonitrile butadiene styrene) composite material and preparation method thereof
CN104987681A (en) Inorganic filler synergistic toughening polyactic acid hybrid material and preparation method thereof
CN107383744A (en) A kind of waste household appliances polypropylene modified material and preparation method thereof
CN103396643A (en) Modifier-containing polyacrylate grafted vinyl chloride composite resin composition
CN100441626C (en) High-toughness polypropylene plastics and its preparing process
CN102286168A (en) Polypropylene/ acrylonitrile styrene (AS) blend and preparation method thereof and thermal treatment method for product
CN102898827A (en) Self-lubricating abrasion-resistant injection-molding grade nylon 66 and preparation technology thereof
CN1218998C (en) Polyethanediol terephthalate composition and its preparation method
Eroglu Effect of talc and heat treatment on the properties of polypropylene/EVA composite
CN107815054A (en) A kind of PA composites and preparation method thereof with low water absorption, strong thermal conductivity
CN106967256A (en) A kind of oil resistivity PET/ABS composites and preparation method thereof
CN108676274A (en) A kind of film and preparation method thereof
EP3135717A1 (en) Fiber-reinforced plastic composition, and fiber-reinforced composite with improved impact performance, prepared therefrom

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
CB03 Change of inventor or designer information

Inventor after: Sang Jie

Inventor after: Yang Guichang

Inventor after: Fang Anping

Inventor before: Wang Canyao

Inventor before: Yu Haiou

Inventor before: Yi Qingfeng

Inventor before: Sang Jie

Inventor before: Yang Guichang

Inventor before: Fang Anping

CB03 Change of inventor or designer information
CP02 Change in the address of a patent holder

Address after: 528300 Longchuang Road, Malong Village Committee, Beijiao Town, Shunde District, Foshan City, Guangdong Province

Patentee after: Guangdong harmony new materials Co. Ltd.

Address before: 528322 No. 10 Factory Building of Tianren Industrial Park, Liandu Village, Leliu Street, Shunde District, Foshan City, Guangdong Province

Patentee before: Guangdong harmony new materials Co. Ltd.

CP02 Change in the address of a patent holder
AV01 Patent right actively abandoned

Granted publication date: 20190301

Effective date of abandoning: 20191120

AV01 Patent right actively abandoned