CN102304248A - Expandable high-melt-strength polypropylene resin and preparation method thereof - Google Patents

Expandable high-melt-strength polypropylene resin and preparation method thereof Download PDF

Info

Publication number
CN102304248A
CN102304248A CN201110253257A CN201110253257A CN102304248A CN 102304248 A CN102304248 A CN 102304248A CN 201110253257 A CN201110253257 A CN 201110253257A CN 201110253257 A CN201110253257 A CN 201110253257A CN 102304248 A CN102304248 A CN 102304248A
Authority
CN
China
Prior art keywords
acrylic resin
rev
forcing machine
machine
high bath
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.)
Granted
Application number
CN201110253257A
Other languages
Chinese (zh)
Other versions
CN102304248B (en
Inventor
胡圣飞
陈长青
欧小波
张冲
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.)
Wuhan Virentia Advanced Material Co., Ltd.
Original Assignee
Hubei University of Technology
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 Hubei University of Technology filed Critical Hubei University of Technology
Priority to CN2011102532574A priority Critical patent/CN102304248B/en
Publication of CN102304248A publication Critical patent/CN102304248A/en
Application granted granted Critical
Publication of CN102304248B publication Critical patent/CN102304248B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • B29C48/395Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders
    • B29C48/40Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders using two or more parallel screws or at least two parallel non-intermeshing screws, e.g. twin screw extruders

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

The invention discloses an expandable high-melt-strength polypropylene resin and a preparation method thereof. The method comprises: reacting and extruding raw materials including polypropylene, ultrahigh molecular weight polyethylene, petroleum resin, hyperoxide, bis[gamma-(triethoxysilyl)propyl]tetrasulfide, zinc oxide, stearic acid and the like in a parallel double screw extruder to obtain high-melt-strength polypropylene; and mixing the high-melt-strength polypropylene with liquid paraffin and azodicarbonamide at a high speed to obtain the expandable high-melt-strength polypropylene resin. The method disclosed by the invention is simple, low in investment and environment-friendly, and the extrusion performance of the melt is high.

Description

A kind of have expandability high bath strength acrylic resin and preparation method thereof
Technical field
The invention belongs to technical field of polymer materials, be specifically related to a kind of expandability high bath strength acrylic resin and preparation method thereof that has.
Background technology
Polypropylene is as a kind of thermoplasticity synthetic resins, have synthetic easily, characteristics such as little, nontoxic, the good heat resistance of density, rigidity height and electrical insulating property excellence, in industries such as automobile, household electrical appliances, packing and building materials, be widely used.But because polypropylene is as a kind of crystal polymer thing; When processing temperature is near its fusing point; Its melt strength descends rapidly; Thereby cause its melt strength low with the hang down shortcoming of poor performance of refractory; Cause its container wall thickness when thermoforming inhomogeneous; During extrusion coated calendering edge curl, contraction appear, abscess problem such as subside during extrusion foaming.Therefore, polypropylene receives very big restriction in the application in fields such as thermoforming, extrusion coated, blowing and foaming.
Polyacrylic foaming process essence is a drawing process of melt polypropylene, and bubble is grown up when foaming, receiving the change alkene characteristic that stretches in addition when stretching, therefore can't be shaped to the polypropylene expanded body with high foamability for the plain polypropylene melt.Given this, exploitation has the expandability high bath strength acrylic resin and has just become the important topic of pendulum in face of the scientific worker.
Abroad (Borealis, Korea S's Hunan chemical industry etc.) at present with the high fondant-strength industrialization, and in global marketing, obtains applications well in the high foaming of polypropylene field especially in thermoforming, extrusion coated, blowing.Domesticly recently also begin the research of high melt strength, propylene, obtained certain effect.But because existing treatment process adopts irradiation method mostly, though the feasible equipment of this method has high input, industrialization at present is few.Research is more in the chemical graft process, but a large amount of organic solvents of the employing that has or easy volatile monomer produce considerable influence to environment, disclose a kind of high bath strength acrylic resin and preparation method thereof like CN1775851A.This high bath strength acrylic resin is by comprising that weight percent is that 30 ~ 80% graft polypropylene, 10 ~ 50% polypropylene, 2 ~ 10% metallocene PE resin, 2 ~ 10% aminated compounds and other auxiliary agent of surplus are formed.Preparing method of the present invention is for after mixing the graft polypropylene resin of formula ratio and homopolymerization, copolymerization PP raw material, metallocene PE resin, various auxiliary agent in the high-speed mixing still; Joining temperature from spout is that 180 ~ 220 ℃, L/D are 36: 1 ~ 48: 1 the twin screw extruder; Add the aminated compounds acetone soln in screw rod the 4th district through precision metering pump, vacuumize granulation and form.
In sum, exploitation have less investment, environmental protection to have an expandability high bath strength acrylic resin imperative.
Summary of the invention
Deficiency in view of prior art; The object of the present invention is to provide a kind of expandability high bath strength acrylic resin and preparation method thereof that has; This polyacrylic melt strength is high, this preparation method in the melt strength that improves acrylic resin, production process environmental protection, feasible.
In order to realize the object of the invention, the contriver has obtained following technical scheme through a large amount of experimental studies:
A kind of have an expandability high bath strength acrylic resin, is prepared from polypropylene, petroleum resin, ultrahigh molecular weight polyethylene(UHMWPE), dicumyl peroxide, two-[γ-(triethoxysilicane) propyl group] tetrasulfide and other auxiliary agent.
In the embodiment of a preparation high bath strength acrylic resin of the present invention, described other auxiliary agents are antioxidant 1010s.Preferably, this high bath strength acrylic resin is prepared from each component by following weight part:
Polypropylene 100 parts
Petroleum resin 1-10 part
Ultrahigh molecular weight polyethylene(UHMWPE) 1-5 part
Dicumyl peroxide 0.1-2 part
Two-[γ-(triethoxysilicane) propyl group] tetrasulfide 0.6-2 part
Antioxidant 1010 0.1-0.5 part.
In the embodiment of another preparation expandability high bath strength acrylic resin of the present invention, described other auxiliary agents are mixtures of antioxidant 1010, zinc oxide, stearic acid, azo two formyl ammonia and whiteruss.Preferably, this expandability high bath strength acrylic resin is prepared from each component by following weight part:
Polypropylene 100 parts
Petroleum resin 1-10 part
Ultrahigh molecular weight polyethylene(UHMWPE) 1-5 part
Dicumyl peroxide 0.1-2 part
Two-[γ-(triethoxysilicane) propyl group] tetrasulfide 0.6-2 part
Antioxidant 1010 0.1-0.5 part
Zinc oxide 1-5 part
Stearic acid 1-5 part
Azo two formyl ammonia 0.1-20 part
Whiteruss; 0.1-0.3 part.
Second purpose of the present invention is the method that provides two kinds to prepare high bath strength acrylic resin:
Method one: the preparation method of high bath strength acrylic resin; Comprise polypropylene; Petroleum resin; Ultrahigh molecular weight polyethylene(UHMWPE); Dicumyl peroxide and two-[γ-(triethoxysilicane) propyl group] tetrasulfide; Antioxidant 1010 in mixing machine with 900-1200 rev/min; 60 ℃ were stirred 15 minutes down; The back adds in the forcing machine of two rank: this pair rank forcing machine wherein single order is a parallel double-screw extruder; The forcing machine length-to-diameter ratio is 40:1; Screw diameter 75 mm; 100-400 rev/min of parallel double-screw extruder rotating speed, the temperature of twin screw extruder from the transportation section to the discharge port is 190-210 ℃; Second rank are single screw extrusion machine; The forcing machine length-to-diameter ratio is 15:1, and screw diameter 150, single screw extrusion machine are rotating speed 25-50 rev/min; Forcing machine is 150-190 ℃ from the transportation section to the temperature of mouth mould and reacts extruding pelletization, obtains a kind of high bath strength acrylic resin.
Method two: preparation method with expandability high bath strength acrylic resin; Comprise polypropylene; Petroleum resin; Ultrahigh molecular weight polyethylene(UHMWPE); Dicumyl peroxide; Two-[γ-(triethoxysilicane) propyl group] tetrasulfide; Antioxidant 1010 and zinc oxide; Stearic acid in mixing machine with 900-1200 rev/min; 60 ℃ were stirred 15 minutes down; The back adds in the forcing machine of two rank: this pair rank forcing machine wherein single order is a parallel double-screw extruder; The forcing machine length-to-diameter ratio is 40:1; Screw diameter 75mm; 100-400 rev/min of parallel double-screw extruder rotating speed, the temperature of twin screw extruder from the transportation section to the discharge port is 190-210 ℃; Second rank are single screw extrusion machine; The forcing machine length-to-diameter ratio is 15:1, and screw diameter 150, single screw extrusion machine are rotating speed 25-50 rev/min; Forcing machine is 150-190 ℃ from the transportation section to the temperature of mouth mould and reacts extruding pelletization, obtains a kind of high bath strength acrylic resin D;
Acrylic resin D and azo two formyl ammonia and whiteruss were stirred 15 minutes down with 900-1200 rev/min, 60 ℃ in mixing machine; Obtain a kind of high bath strength acrylic resin E with expandability; Acrylic resin E is added in the single screw extrusion machine; Rotating speed 20-30 rev/min; Single screw extrusion machine is 160-210 ℃ from the transportation section to the temperature of mouth mould; Extrusion foaming can obtain extruding the polypropylene expanded body of homogeneous.
Polypropylene of the present invention comprises the disclosed various types of acrylic resins of prior art, comprises homo-polypropylene resin, Co-polypropylene resin etc.
Ultrahigh molecular weight polyethylene(UHMWPE) of the present invention refers to the Vilaterm of molecular-weight average at 250-350 ten thousand.The high melt strength, propylene that its existence can effectively prevent to be invented is in extrusion, and viscosity occurs than great fluctuation process.
Petroleum resin of the present invention refer to the copolymer resins of the alicyclic C 5 petroleum resin of dicyclopentadiene, C 5/C nine copolymerized petroleum resins, carbon five and other material.Petroleum resin are as crosslinking coagent, and its adding can promote the combination between the polypropylene macromole, form long branched chain structure.
Of the present invention pair-[γ-(triethoxysilicane) propyl group] tetrasulfide (Si-69), it mainly acts on is the effect of in the process of preparation branched p 0 lypropylene, playing stabilized radical.In the preparation process, the tertiary carbon macromolecular radical that polypropylene forms is unstable, and at high temperature, do not have under the situation of Si-69 auxiliary agent, polyacrylic degraded plays a leading role, and causes degradation of polypropylene serious; And under the situation that the Si-69 auxiliary agent is arranged, can reduce the concentration of polypropylene macromolecular radical, and suppress polyacrylic degraded, help polypropylene branching or little crosslinked.
Whiteruss of the present invention is No. 5 white oils, and its adding helps the polypropylene surface that obtained high fondant-strength is dispersed and sticked to whipping agent.
Compared with prior art, a kind of acrylic resin that the present invention relates to and preparation method thereof has following advantage and marked improvement: (1) melt polypropylene degree is high, and its melt strength is 5 times of plain polypropylene.(2) no volatile solvent in the course of processing.(3) the material foam performance is good, and foam density is less than 0.2 gram/cubic centimetre during extrusion foaming.
Embodiment
Further specify the present invention through embodiment below.The preparation method of the embodiment of the invention is only used for illustrating the present invention, rather than limitation of the present invention, under design prerequisite of the present invention, preparing method's of the present invention simple modifications is all belonged to the present invention and requires the scope protected.
The preparation of embodiment one high bath strength acrylic resin
Figure 686712DEST_PATH_IMAGE002
Method one: will form polypropylene among the A, petroleum resin, ultrahigh molecular weight polyethylene(UHMWPE), dicumyl peroxide and two-[γ-(triethoxysilicane) propyl group] tetrasulfide, oxidation inhibitor by proportioning and in mixing machine, stir 15 minutes down with 900-1200 rev/min, 60 ℃; The back adds in the forcing machine of two rank: this pair rank forcing machine wherein single order is a parallel double-screw extruder; The forcing machine length-to-diameter ratio is 40:1; Screw diameter 75; 100-400 rev/min of parallel double-screw extruder rotating speed, the temperature of twin screw extruder from the transportation section to the discharge port is 190-210 ℃.Second rank are single screw extrusion machine; The forcing machine length-to-diameter ratio is 15:1, and screw diameter 150, single screw extrusion machine are 25-50 rev/mins of rotating speeds; Forcing machine is 150-190 ℃ from the transportation section to the temperature of mouth mould and reacts extruding pelletization, obtains a kind of high bath strength acrylic resin.
Method two: by proportioning will form A with form among the B raw material in mixing machine with 900-1200 rev/min, 60 ℃ stirrings 15 minutes down; The back adds in the forcing machine of two rank: this pair rank forcing machine wherein single order is a parallel double-screw extruder; The forcing machine length-to-diameter ratio is 40:1; Screw diameter 75; 100-400 rev/min of parallel double-screw extruder rotating speed, the temperature of twin screw extruder from the transportation section to the discharge port is 190-210 ℃.Second rank are single screw extrusion machine; The forcing machine length-to-diameter ratio is 15:1, and screw diameter 150, single screw extrusion machine are 25-50 rev/mins of rotating speeds; Forcing machine is 150-190 ℃ from the transportation section to the temperature of mouth mould and reacts extruding pelletization, obtains a kind of high bath strength acrylic resin D.
In proportion resin D and composition C were stirred 15 minutes down with 900-1200 rev/min, 60 ℃ in mixing machine again; Obtain a kind of high bath strength acrylic resin E with expandability; E is added in the single screw extrusion machine; 30 rev/mins of rotating speeds; Single screw extrusion machine is 160-210 ℃ from the transportation section to the temperature of mouth mould; Extrusion foaming can obtain extruding the polypropylene expanded body of homogeneous.According to the sample of this method preparation have compared with prior art that the melt polypropylene degree is high, advantage such as no volatile solvent in the course of processing, material foam performance are good; Its melt strength is 5 times of plain polypropylene, and foam density is less than 0.2 gram/cubic centimetre during extrusion foaming.
The preparation of embodiment two high bath strength acrylic resins
Its preparation method is with embodiment one.
The preparation of embodiment three high bath strength acrylic resins
Change homo-polypropylene into homo-polypropylene and the polyacrylic mixture of copolymerization, homo-polypropylene accounts for 1-99% in the mixture, and making method is with embodiment one.

Claims (7)

1. one kind has the expandability high bath strength acrylic resin, it is characterized in that: be prepared from polypropylene, petroleum resin, ultrahigh molecular weight polyethylene(UHMWPE), dicumyl peroxide, two-[γ-(triethoxysilicane) propyl group] tetrasulfide and other auxiliary agent.
2. according to claim 1 have an expandability high bath strength acrylic resin, and it is characterized in that: described other auxiliary agents are antioxidant 1010s.
3. according to claim 2 have an expandability high bath strength acrylic resin, and it is characterized in that: each component by following weight part is prepared from:
Figure 3
4. according to claim 1 have an expandability high bath strength acrylic resin, and it is characterized in that: described other auxiliary agents are mixtures of antioxidant 1010, zinc oxide, stearic acid, azo two formyl ammonia and whiteruss.
5. according to claim 4 have an expandability high bath strength acrylic resin, and it is characterized in that: each component by following weight part is prepared from:
Figure 224281DEST_PATH_IMAGE004
6. claim 2 or 3 described preparing methods with expandability high bath strength acrylic resin; It is characterized in that: with polypropylene; Petroleum resin; Ultrahigh molecular weight polyethylene(UHMWPE); Dicumyl peroxide and two-[γ-(triethoxysilicane) propyl group] tetrasulfide; Antioxidant 1010 in mixing machine with 900-1200 rev/min; 60 ℃ were stirred 15 minutes down; The back adds in the forcing machine of two rank: this pair rank forcing machine wherein single order is a parallel double-screw extruder; The forcing machine length-to-diameter ratio is 40:1; Screw diameter 75 mm; 100-400 rev/min of parallel double-screw extruder rotating speed, the temperature of twin screw extruder from the transportation section to the discharge port is 190-210 ℃; Second rank are single screw extrusion machine; The forcing machine length-to-diameter ratio is 15:1, and screw diameter 150, single screw extrusion machine are rotating speed 25-50 rev/min; Forcing machine is 150-190 ℃ from the transportation section to the temperature of mouth mould and reacts extruding pelletization, obtains a kind of high bath strength acrylic resin.
7. claim 2 or 3 described preparing methods with expandability high bath strength acrylic resin; It is characterized in that: with polypropylene; Petroleum resin; Ultrahigh molecular weight polyethylene(UHMWPE); Dicumyl peroxide; Two-[γ-(triethoxysilicane) propyl group] tetrasulfide; Antioxidant 1010 and zinc oxide; Stearic acid in mixing machine with 900-1200 rev/min; 60 ℃ were stirred 15 minutes down; The back adds in the forcing machine of two rank: this pair rank forcing machine wherein single order is a parallel double-screw extruder; The forcing machine length-to-diameter ratio is 40:1; Screw diameter 75mm; 100-400 rev/min of parallel double-screw extruder rotating speed, the temperature of twin screw extruder from the transportation section to the discharge port is 190-210 ℃; Second rank are single screw extrusion machine; The forcing machine length-to-diameter ratio is 15:1, and screw diameter 150, single screw extrusion machine are rotating speed 25-50 rev/min; Forcing machine is 150-190 ℃ from the transportation section to the temperature of mouth mould and reacts extruding pelletization, obtains a kind of high bath strength acrylic resin D;
Acrylic resin D and azo two formyl ammonia and whiteruss were stirred 15 minutes down with 900-1200 rev/min, 60 ℃ in mixing machine; Obtain a kind of high bath strength acrylic resin E with expandability; Acrylic resin E is added in the single screw extrusion machine; Rotating speed 20-30 rev/min; Single screw extrusion machine is 160-210 ℃ from the transportation section to the temperature of mouth mould; Extrusion foaming can obtain extruding the polypropylene expanded body of homogeneous.
CN2011102532574A 2011-08-31 2011-08-31 Expandable high-melt-strength polypropylene resin and preparation method thereof Expired - Fee Related CN102304248B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2011102532574A CN102304248B (en) 2011-08-31 2011-08-31 Expandable high-melt-strength polypropylene resin and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2011102532574A CN102304248B (en) 2011-08-31 2011-08-31 Expandable high-melt-strength polypropylene resin and preparation method thereof

Publications (2)

Publication Number Publication Date
CN102304248A true CN102304248A (en) 2012-01-04
CN102304248B CN102304248B (en) 2013-08-14

Family

ID=45378172

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2011102532574A Expired - Fee Related CN102304248B (en) 2011-08-31 2011-08-31 Expandable high-melt-strength polypropylene resin and preparation method thereof

Country Status (1)

Country Link
CN (1) CN102304248B (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103923382A (en) * 2014-03-14 2014-07-16 湖北工业大学 Foamed polypropylene bead with low melting point and high cementability and preparation method thereof
CN104610506A (en) * 2015-01-04 2015-05-13 南通日之升高分子新材料科技有限公司 High-melt strength polypropylene and preparation method thereof
CN106279965A (en) * 2015-06-11 2017-01-04 合肥杰事杰新材料股份有限公司 A kind of physical blowing fills anti-flaming polypropylene material and preparation method thereof
CN106750992A (en) * 2016-12-15 2017-05-31 广东圆融新材料有限公司 A kind of low gloss, low-odor polypropylene ene compositions and preparation method thereof
CN107163477A (en) * 2017-05-26 2017-09-15 合肥会通新材料有限公司 One kind can directly be molded chemical micro-foaming polypropylene composite material and preparation method thereof
CN109762229A (en) * 2018-12-24 2019-05-17 浙江万里新材料科技有限公司 A kind of Radiation Crosslinked Polyethylene foam material and preparation method thereof
CN109777064A (en) * 2017-11-14 2019-05-21 万华化学集团股份有限公司 A kind of extrusion grade Polycarbonate alloy material and its preparation method and application
CN109824955A (en) * 2018-12-24 2019-05-31 浙江万里新材料科技有限公司 A kind of Radiation Crosslinked Polyethylene foam material and preparation method thereof
CN111117073A (en) * 2020-01-09 2020-05-08 山东清河化工科技有限公司 Blending type ultrahigh molecular weight polypropylene/polypropylene alloy and preparation method thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1127272A (en) * 1995-10-05 1996-07-24 中国石化茂名石油化工公司 Polypropylene toughness-increasing modified material and preparing method
EP0889087B1 (en) * 1997-07-01 2002-05-08 Buna Sow Leuna Olefinverbund GmbH Moulding material based on polyethylene of ultra-high molecular weight and its production
CN1453306A (en) * 2003-05-13 2003-11-05 北京度辰新材料股份有限公司 High-intercluding transparent polypropylene resin composition, sheet made of the composition and its making process
CN101735545A (en) * 2009-12-29 2010-06-16 丹阳市华东工程塑料有限公司 High rigidity light composite board for automobile roof and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1127272A (en) * 1995-10-05 1996-07-24 中国石化茂名石油化工公司 Polypropylene toughness-increasing modified material and preparing method
EP0889087B1 (en) * 1997-07-01 2002-05-08 Buna Sow Leuna Olefinverbund GmbH Moulding material based on polyethylene of ultra-high molecular weight and its production
CN1453306A (en) * 2003-05-13 2003-11-05 北京度辰新材料股份有限公司 High-intercluding transparent polypropylene resin composition, sheet made of the composition and its making process
CN101735545A (en) * 2009-12-29 2010-06-16 丹阳市华东工程塑料有限公司 High rigidity light composite board for automobile roof and preparation method thereof

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103923382A (en) * 2014-03-14 2014-07-16 湖北工业大学 Foamed polypropylene bead with low melting point and high cementability and preparation method thereof
CN103923382B (en) * 2014-03-14 2016-04-06 湖北工业大学 A kind of low melting point height can cementability expanded polypropylene beads and preparation method thereof
CN104610506A (en) * 2015-01-04 2015-05-13 南通日之升高分子新材料科技有限公司 High-melt strength polypropylene and preparation method thereof
CN106279965A (en) * 2015-06-11 2017-01-04 合肥杰事杰新材料股份有限公司 A kind of physical blowing fills anti-flaming polypropylene material and preparation method thereof
CN106750992B (en) * 2016-12-15 2019-03-01 广东圆融新材料有限公司 A kind of low gloss, low-odor polypropylene ene compositions and preparation method thereof
CN106750992A (en) * 2016-12-15 2017-05-31 广东圆融新材料有限公司 A kind of low gloss, low-odor polypropylene ene compositions and preparation method thereof
CN107163477A (en) * 2017-05-26 2017-09-15 合肥会通新材料有限公司 One kind can directly be molded chemical micro-foaming polypropylene composite material and preparation method thereof
CN109777064A (en) * 2017-11-14 2019-05-21 万华化学集团股份有限公司 A kind of extrusion grade Polycarbonate alloy material and its preparation method and application
CN109777064B (en) * 2017-11-14 2021-07-23 万华化学集团股份有限公司 Extrusion-grade polycarbonate alloy material and preparation method and application thereof
CN109762229A (en) * 2018-12-24 2019-05-17 浙江万里新材料科技有限公司 A kind of Radiation Crosslinked Polyethylene foam material and preparation method thereof
CN109824955A (en) * 2018-12-24 2019-05-31 浙江万里新材料科技有限公司 A kind of Radiation Crosslinked Polyethylene foam material and preparation method thereof
CN109824955B (en) * 2018-12-24 2021-07-06 浙江万里新材料科技有限公司 Irradiation crosslinking polyethylene foam material and preparation method thereof
CN111117073A (en) * 2020-01-09 2020-05-08 山东清河化工科技有限公司 Blending type ultrahigh molecular weight polypropylene/polypropylene alloy and preparation method thereof

Also Published As

Publication number Publication date
CN102304248B (en) 2013-08-14

Similar Documents

Publication Publication Date Title
CN102304248B (en) Expandable high-melt-strength polypropylene resin and preparation method thereof
CN104403175A (en) Permanently anti-static polyolefin master batch and preparation method thereof
CN103360656B (en) A kind of regenerated polythene composition and method of making the same
CN107082977A (en) A kind of high-impact high fluidity PVC injected plastics materials formula and preparation method thereof
CN102190841A (en) Preparation method of high-performance chlorinated polyvinyl chloride injection aggregate
CN105086088A (en) Polyethylene composite plastic particles
CN105713315A (en) Formula for synthesizing novel high-polymer fiber composite materials
CN104087211A (en) Adhesive for anticorrosive paint for deep-sea oil-gas delivery steel tube outer walls and preparation method thereof
CN111073273A (en) Glass fiber reinforced PA6 composite material for improving floating fiber and high surface smoothness and preparation method thereof
CN102585332A (en) Modified ultra-high molecular weight polyethylene material
CN105385121A (en) Polyester composition used for nanometer injection molding and preparing method thereof
Khonakdar et al. Thermal and mechanical properties of uncrosslinked and chemically crosslinked polyethylene/ethylene vinyl acetate copolymer blends
CN109880445B (en) High-adhesion polyethylene powder coating and preparation method and application thereof
CN102108146B (en) Polyolefin thermoplastic elastomer (TPE) composition and preparation method thereof
CN105623106B (en) Rub resistance, the modified random copolymerization of resistance to scratch polypropylene material and preparation method thereof
CN111040307A (en) Polypropylene corrugated pipe composite material and preparation method of composite polypropylene corrugated pipe
CN105037951A (en) Inorganic rigid particle three-element blend toughened system RRP (polypropylene random) tube and preparation method thereof
CN101717544B (en) Black polypropylene anti-corrosive material and method for preparing same
CN108047573B (en) Special material for PPR (polypropylene random) pipe and preparation method thereof
CN108727809A (en) A kind of hollow blow molding nylon micro-foaming material and preparation method thereof
Zheng et al. Preparation and characterization of starch/EVA composite foams with surface modified kaolin
CN106519372A (en) Antistatic extruded HDPE tube raw material for coal mine and preparation method of antistatic extruded HDPE tube raw material
KR102711173B1 (en) Powder additive comprising cross-linked resin and resin composition comprising the same
CN1282699C (en) Radiation crosslinked polyethylene pipe and its preparation method
CN101117372A (en) High fondant-strength profax 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
ASS Succession or assignment of patent right

Owner name: WUHAN VIRENTIA ADVANCED MATERIAL CO., LTD.

Free format text: FORMER OWNER: HUBEI INDUSTRY UNIVERSITY

Effective date: 20130329

Owner name: HUBEI INDUSTRY UNIVERSITY

Effective date: 20130329

C41 Transfer of patent application or patent right or utility model
COR Change of bibliographic data

Free format text: CORRECT: ADDRESS; FROM: 430068 WUHAN, HUBEI PROVINCE TO: 430223 WUHAN, HUBEI PROVINCE

TA01 Transfer of patent application right

Effective date of registration: 20130329

Address after: 430223 innovation building, Hua Cheng Science Park, No. 5, Hua Shi Road, East Lake Development Zone, Wuhan, Hubei

Applicant after: Wuhan Virentia Advanced Material Co., Ltd.

Applicant after: Hubei Industry University

Address before: 430068, No. 1, Li Jia Tun, Nanhu Lake, Hongshan District, Hubei, Wuhan

Applicant before: Hubei Industry University

C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20130814

Termination date: 20190831

CF01 Termination of patent right due to non-payment of annual fee