CN109054186A - A kind of Functional Polyolefine solid degradation agent - Google Patents

A kind of Functional Polyolefine solid degradation agent Download PDF

Info

Publication number
CN109054186A
CN109054186A CN201810975809.4A CN201810975809A CN109054186A CN 109054186 A CN109054186 A CN 109054186A CN 201810975809 A CN201810975809 A CN 201810975809A CN 109054186 A CN109054186 A CN 109054186A
Authority
CN
China
Prior art keywords
degradation agent
antioxidant
functional polyolefine
functional
solid degradation
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
CN201810975809.4A
Other languages
Chinese (zh)
Other versions
CN109054186B (en
Inventor
赵立阳
任国辉
姜晋良
吴宪
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.)
DALIAN XINGHUI CHEMICAL Co.,Ltd.
Original Assignee
DALIAN XINGHUI CHEMICAL 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 DALIAN XINGHUI CHEMICAL CO LTD filed Critical DALIAN XINGHUI CHEMICAL CO LTD
Priority to CN201810975809.4A priority Critical patent/CN109054186B/en
Publication of CN109054186A publication Critical patent/CN109054186A/en
Application granted granted Critical
Publication of CN109054186B publication Critical patent/CN109054186B/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
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/20Compounding polymers with additives, e.g. colouring
    • C08J3/22Compounding polymers with additives, e.g. colouring using masterbatch techniques
    • C08J3/226Compounding polymers with additives, e.g. colouring using masterbatch techniques using a polymer as a carrier
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2323/00Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2323/02Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
    • C08J2323/10Homopolymers or copolymers of propene
    • C08J2323/12Polypropene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2353/00Characterised by the use of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2423/00Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2423/02Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
    • C08J2423/10Homopolymers or copolymers of propene
    • C08J2423/12Polypropene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/017Additives being an antistatic agent
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/09Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • C08K5/098Metal salts of carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/13Phenols; Phenolates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/14Peroxides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/20Carboxylic acid amides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/34Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3477Six-membered rings
    • C08K5/3492Triazines
    • C08K5/34924Triazines containing cyanurate groups; Tautomers thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/49Phosphorus-containing compounds
    • C08K5/51Phosphorus bound to oxygen
    • C08K5/52Phosphorus bound to oxygen only
    • C08K5/524Esters of phosphorous acids, e.g. of H3PO3
    • C08K5/526Esters of phosphorous acids, e.g. of H3PO3 with hydroxyaryl compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

The present invention relates to a kind of Functional Polyolefine solid degradation agents, belong to degradation agent technical field.Functional Polyolefine solid degradation agent of the present invention is made of following components by weight: 30-70 parts of polypropylene, 5-20 parts of peroxide, 10-30 parts of antioxidant, slipping agent/5-15 parts of antistatic agent, 5-15 parts of acid scavenger;Wherein: the peroxide is at least one of two t-amyl peroxy compounds, -2,5 bis(t-butylperoxy) hexane of 2,5- dimethyl and cumyl peroxide.The high melting means polypropylene product narrow molecular weight distribution produced using Functional Polyolefine solid degradation agent of the present invention, meanwhile, there is excellent antioxygenic property, at 200 DEG C, the oxidation induction period of product is greater than 8min.

Description

A kind of Functional Polyolefine solid degradation agent
Technical field
The present invention relates to a kind of Functional Polyolefine solid degradation agents, belong to degradation agent technical field.
Background technique
The polypropylene fibre of high quality requires polypropylene product to have higher melt index and narrow molecular weight distribution.It is usually raw The polypropylene product that production meets the requirement needs to use edman degradation Edman, that is, passes through the polypropylene product in wide molecular weight low melt index Degradation agent is added during extruding pelletization to realize the polypropylene product of production narrow molecular weight distribution and high melt index.
In the high melting means polymarization method for prodcing polyacrylates of edman degradation Edman production, the organic peroxide of liquid is commonly used as degradation agent.By Concentration is higher when liquid peroxide is in addition, and additive amount is small, is uniformly dispersed in degradation agent in polymer relatively more tired It is difficult.If the melt index for dispersing unevenly to may cause product is unstable, homogeneity is poor, continuous production and product are influenced The stability of quality, the local excessive degradation as caused by dispersion is uneven can make product generate smell, in addition also mention peroxide Since its higher chemical activity makes it, there are higher risk during transport, storage and use, easily burn very To exploding.
Summary of the invention
The present invention solves the above problem by providing a kind of new solid degradation agent.
The present invention provides a kind of Functional Polyolefine solid degradation agent, the Functional Polyolefine solid degradation agent is pressed Parts by weight are made of following components:
Wherein: the peroxide be two t-amyl peroxy compounds, -2,5 bis(t-butylperoxy) of 2,5- dimethyl oneself At least one of alkane and cumyl peroxide.
Peroxide of the present invention is most preferably -2,5 bis(t-butylperoxy) hexane of 2,5- dimethyl.
The present invention is preferably that the antioxidant is antioxidant 3114, antioxidant 330, antioxidant 1010, irgasfos 168, resists At least one of oxygen agent 1076 and antioxidant 264.
The present invention is preferably that the antioxidant is antioxidant 3114, antioxidant 330 and irgasfos 168.
The present invention is preferably that the weight ratio of the antioxidant 3114, antioxidant 330 and irgasfos 168 is 1:1:0.2-5.
The weight ratio of antioxidant 3114 of the present invention, antioxidant 330 and irgasfos 168 is most preferably 1:1:1.
The present invention is preferably that the slipping agent/antistatic agent is monoglyceride, erucyl amide or oleamide.
Slipping agent/antistatic agent of the present invention is most preferably monoglyceride.
The present invention is preferably that the acid scavenger is calcium stearate or zinc stearate.
Acid scavenger of the present invention is most preferably calcium stearate.
The present invention is preferably the polypropylene under 230 DEG C of temperature, pressure 2.16kg, melt index 1-10g/ 10min。。
The present invention is preferably the shape of the Functional Polyolefine solid degradation agent for cylinder, and the basal diameter of cylinder is 1-5mm, the height of cylinder are 1-10mm.
The present invention is preferably that the Functional Polyolefine solid degradation agent additive amount is polyacrylic 0.1-8wt.%.
The invention has the following beneficial effects:
Functional Polyolefine solid degradation agent of the present invention can in an extruder it is evenly dispersed in the polymer, make to gather The degradation process for closing object is more uniform, meanwhile, the small molecule of generation is few, smell is small, and the product melt index after degradation is more steady It is fixed.
The high melting means polypropylene product molecular weight distribution produced using Functional Polyolefine solid degradation agent of the present invention It is narrow, meanwhile, there is excellent antioxygenic property, at 200 DEG C, the oxidation induction period of product is greater than 8min.
Functional Polyolefine solid degradation agent of the present invention is not limited to producing the application in high melting means polypropylene product, Also suitable for the production process of other thermoplastic articles produced using edman degradation Edman.
Specific embodiment
Following non-limiting embodiments can with a person of ordinary skill in the art will more fully understand the present invention, but not with Any mode limits the present invention.
Following polypropylene are under 230 DEG C of temperature, pressure 2.16kg, melt index 3g/10min.
Following peroxide are -2,5 bis(t-butylperoxy) hexane of 2,5- dimethyl.
Following antioxidant are antioxidant 3114, antioxidant 330 and irgasfos 168, the antioxidant 3114, antioxidant 330 Weight ratio with irgasfos 168 is 1:1:1.
Following slipping agent/antistatic agents are monoglyceride.
Following acid scavengers are calcium stearate.
Following conventional solid degradation agents are solid degradation agent disclosed in application publication number CN 102358791A.
Following homopolypropylene T30S are under 230 DEG C of temperature, pressure 2.16kg, melt index 2.9g/10min.
Following atactic copolymerized polypropene L6D20 are under 230 DEG C of temperature, pressure 2.16kg, melt index 1.9g/10min.
Following block copolymerization polypropylene EPS30R are under 230 DEG C of temperature, pressure 2.16kg, melt index 2g/10min.
Following melt index test reference GB/T 3682-2000.
Following oxidation induction period test reference GB/T 19466.6-2009.
Embodiment 1
A kind of preparation method of Functional Polyolefine solid degradation agent, the preparation method is that: it is by weight, poly- by 70 parts Propylene, 10 parts of peroxide, 20 parts of antioxidant, 5 parts of slipping agent/antistatic agents are squeezed out in extruder with 5 parts of acid scavengers and are made Grain obtains cylindrical Functional Polyolefine solid degradation agent particle, and the diameter of bottom cylindrical face is 2-4mm, and the height of cylinder is 2- 4mm。
Application examples 1
The polyacrylic preparation of the high melting means of homopolymerization
Conventional solid degradation agent, antioxidant, slipping agent/antistatic agent, acid scavenger and homopolypropylene material T30S are mixed It closes, the additive amount of the conventional solid degradation agent is 0.5wt.%, and the additive amount of the antioxidant is 0.24wt.%, described refreshing Lubrication prescription/antistatic agent additive amount is 0.05wt.%, and the additive amount of the acid scavenger is 0.05wt.%, is melted in an extruder Melt granulation, obtains the high melting means polypropylene of homopolymerization (comparison product 1), extract 11 samples and carry out melt index test, the result is shown in tables 1。
Application examples 2
The polyacrylic preparation of the high melting means of homopolymerization
With the difference of application examples 1 are as follows: the additive amount of the conventional solid degradation agent is 0.6wt.%, obtains the high melting means of homopolymerization Polypropylene (comparison product 2).
Application examples 3
The polyacrylic preparation of the high melting means of homopolymerization
With the difference of application examples 1 are as follows: the additive amount of the conventional solid degradation agent is that 0.7wt.% obtains the high melting means of homopolymerization Polypropylene (comparison product 3).
Application examples 4
The polyacrylic preparation of the high melting means of homopolymerization
Functional Polyolefine solid degradation agent prepared by embodiment 1 is mixed with homopolypropylene material T30S, the function Property solid olefin degradation agent additive amount be 1.2wt.%, melt pelletization, obtains the high melting means polypropylene of homopolymerization in an extruder (sample 1) extracts 11 samples and carries out melt index test, and the result is shown in tables 1.
Application examples 5
The polyacrylic preparation of the high melting means of homopolymerization
With the difference of application examples 4 are as follows: the additive amount of the Functional Polyolefine solid degradation agent is 1.3wt.%, is obtained Gather high melting means polypropylene (sample 2).
Application examples 6
The polyacrylic preparation of the high melting means of homopolymerization
With the difference of application examples 4 are as follows: the additive amount of the Functional Polyolefine solid degradation agent is 1.4wt.%, is obtained Gather high melting means polypropylene (sample 3).
The polyacrylic melt index test result of the high melting means of 1 homopolymerization of table
Application examples 7
The polyacrylic preparation of the high melting means of random copolymerization
By conventional solid degradation agent, antioxidant, slipping agent/antistatic agent, acid scavenger and atactic copolymerized polypropene material L6D20 mixing, the additive amount of the conventional solid degradation agent are 0.5wt.%, and the additive amount of the antioxidant is 0.24wt.%, The additive amount of the slipping agent/antistatic agent is 0.05wt.%, and the additive amount of the acid scavenger is 0.05wt.%, is being squeezed out Melt pelletization in machine obtains the high melting means polypropylene of random copolymerization (comparison product 4), extracts 11 samples and carry out melt index test, The result is shown in tables 2.
Application examples 8
The polyacrylic preparation of the high melting means of random copolymerization
With the difference of application examples 7 are as follows: the additive amount of the conventional solid degradation agent is 0.6wt.%, obtains random copolymerization height Melting means polypropylene (comparison product 5).
Application examples 9
The polyacrylic preparation of the high melting means of random copolymerization
With the difference of application examples 7 are as follows: the additive amount of the conventional solid degradation agent is 0.7wt.%, obtains random copolymerization height Melting means polypropylene (comparison product 6).
Application examples 10
The polyacrylic preparation of the high melting means of random copolymerization
Functional Polyolefine solid degradation agent prepared by embodiment 1 is mixed with atactic copolymerized polypropene material L6D20, it is described The additive amount of Functional Polyolefine solid degradation agent is 1.2wt.%, and melt pelletization, obtains random copolymerization Gao Rong in an extruder Refer to polypropylene (sample 4), extracts 11 samples and carry out melt index test, the result is shown in tables 2.
Application examples 11
The polyacrylic preparation of the high melting means of random copolymerization
With the difference of application examples 10 are as follows: the additive amount of the Functional Polyolefine solid degradation agent is 1.3wt.%, is obtained The high melting means polypropylene (sample 5) of random copolymerization.
Application examples 12
The polyacrylic preparation of the high melting means of random copolymerization
With the difference of application examples 10 are as follows: the additive amount of the Functional Polyolefine solid degradation agent is 1.4wt.%, is obtained The high melting means polypropylene (sample 6) of random copolymerization.
Table 2 is copolymerized the polyacrylic melt index test result of high melting means
Application examples 13
The polyacrylic preparation of the high melting means of block copolymerization
By conventional solid degradation agent, antioxidant, slipping agent/antistatic agent, acid scavenger and block copolymerization polypropylene material The additive amount of EPS30R mixing, the conventional solid degradation agent is 0.5wt.%, and the additive amount of the antioxidant is The additive amount of 0.24wt.%, the slipping agent/antistatic agent are 0.05wt.%, and the additive amount of the acid scavenger is 0.05wt.%, in an extruder melt pelletization obtain the high melting means polypropylene of block copolymerization (comparison product 7), extract 11 samples into The test of row melt index, the result is shown in tables 3.
Application examples 14
The polyacrylic preparation of the high melting means of block copolymerization
With the difference of application examples 13 are as follows: the additive amount of the conventional solid degradation agent is 0.6wt.%, obtains block copolymerization High melting means polypropylene (comparison product 8).
Application examples 15
The polyacrylic preparation of the high melting means of block copolymerization
With the difference of application examples 13 are as follows: the additive amount of the conventional solid degradation agent is 0.7wt.%, obtains block copolymerization High melting means polypropylene (comparison product 9).
Application examples 16
The polyacrylic preparation of the high melting means of block copolymerization
Functional Polyolefine solid degradation agent prepared by embodiment 1 is mixed with block copolymerization polypropylene material EPS30R, institute The additive amount for stating Functional Polyolefine solid degradation agent is 1.2wt.%, and melt pelletization, obtains block copolymerization height in an extruder Melting means polypropylene (sample 7) extracts 11 samples and carries out melt index test, and the result is shown in tables 3.
Application examples 17
The polyacrylic preparation of the high melting means of block copolymerization
With the difference of application examples 16 are as follows: the additive amount of the Functional Polyolefine solid degradation agent is 1.3wt.%, is obtained The high melting means polypropylene (sample 8) of block copolymerization.
Application examples 18
The polyacrylic preparation of the high melting means of block copolymerization
With the difference of application examples 16 are as follows: the additive amount of the Functional Polyolefine solid degradation agent is 1.4wt.%, is obtained The high melting means polypropylene (sample 9) of block copolymerization.
The polyacrylic melt index test result of the high melting means of 3 block copolymerization of table
The product of application examples 1-18 preparation tests its oxidation induction period, the results are shown in Table 4 at 200 DEG C.
Oxidation induction time of the product of 4 application examples 1-18 of table preparation at 200 DEG C

Claims (9)

1. a kind of Functional Polyolefine solid degradation agent, it is characterised in that: the Functional Polyolefine solid degradation agent, by weight Part, it is made of following components:
Wherein: the peroxide be two t-amyl peroxy compounds, -2,5 bis(t-butylperoxy) hexane of 2,5- dimethyl and At least one of cumyl peroxide.
2. Functional Polyolefine solid degradation agent according to claim 1, it is characterised in that: the antioxidant is antioxidant 3114, at least one of antioxidant 330, antioxidant 1010, irgasfos 168, antioxidant 1076 and antioxidant 264.
3. Functional Polyolefine solid degradation agent according to claim 2, it is characterised in that: the antioxidant is antioxidant 3114, antioxidant 330 and irgasfos 168.
4. Functional Polyolefine solid degradation agent according to claim 3, it is characterised in that: the antioxidant 3114 resists The weight ratio of oxygen agent 330 and irgasfos 168 is 1:1:0.2-5.
5. Functional Polyolefine solid degradation agent according to claim 4, it is characterised in that: the slipping agent/antistatic Agent is monoglyceride, erucyl amide or oleamide.
6. Functional Polyolefine solid degradation agent according to claim 5, it is characterised in that: the acid scavenger is tristearin Sour calcium or zinc stearate.
7. Functional Polyolefine solid degradation agent according to claim 6, it is characterised in that: the polypropylene is in temperature 230 DEG C, under pressure 2.16kg, melt index 1-10g/10min.
8. Functional Polyolefine solid degradation agent according to claim 7, it is characterised in that: the Functional Polyolefine is solid The shape of body degradation agent is cylinder, and the basal diameter of cylinder is 1-5mm, and the height of cylinder is 1-10mm.
9. Functional Polyolefine solid degradation agent according to claim 8, it is characterised in that: the Functional Polyolefine is solid Body degradation agent additive amount is polyacrylic 0.1-8wt.%.
CN201810975809.4A 2018-08-24 2018-08-24 Functional polyolefin solid degradation agent Active CN109054186B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810975809.4A CN109054186B (en) 2018-08-24 2018-08-24 Functional polyolefin solid degradation agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810975809.4A CN109054186B (en) 2018-08-24 2018-08-24 Functional polyolefin solid degradation agent

Publications (2)

Publication Number Publication Date
CN109054186A true CN109054186A (en) 2018-12-21
CN109054186B CN109054186B (en) 2021-09-14

Family

ID=64756989

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810975809.4A Active CN109054186B (en) 2018-08-24 2018-08-24 Functional polyolefin solid degradation agent

Country Status (1)

Country Link
CN (1) CN109054186B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112080072A (en) * 2020-09-15 2020-12-15 惠州莹光塑胶颜料有限公司 Polypropylene composition
CN114163730A (en) * 2021-12-27 2022-03-11 锦州英诺威科技服务有限公司 Polypropylene controllable rheological modifier and preparation method thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0185434A2 (en) * 1984-12-19 1986-06-25 Shell Internationale Researchmaatschappij B.V. Controlled cracking of alpha-olefin polymers
CN1451689A (en) * 2003-05-09 2003-10-29 东华大学 Superhigh melt index polypropene and preparing process thereof
CN101429308A (en) * 2007-11-08 2009-05-13 中国石油天然气股份有限公司 Method for manufacturing polypropylene degradation master batch
CN102358791A (en) * 2011-08-05 2012-02-22 大连兴辉化工有限公司 Solid degradation agent for producing polypropylene fiber with high fusion index, and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0185434A2 (en) * 1984-12-19 1986-06-25 Shell Internationale Researchmaatschappij B.V. Controlled cracking of alpha-olefin polymers
CN1451689A (en) * 2003-05-09 2003-10-29 东华大学 Superhigh melt index polypropene and preparing process thereof
CN101429308A (en) * 2007-11-08 2009-05-13 中国石油天然气股份有限公司 Method for manufacturing polypropylene degradation master batch
CN102358791A (en) * 2011-08-05 2012-02-22 大连兴辉化工有限公司 Solid degradation agent for producing polypropylene fiber with high fusion index, and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112080072A (en) * 2020-09-15 2020-12-15 惠州莹光塑胶颜料有限公司 Polypropylene composition
CN114163730A (en) * 2021-12-27 2022-03-11 锦州英诺威科技服务有限公司 Polypropylene controllable rheological modifier and preparation method thereof

Also Published As

Publication number Publication date
CN109054186B (en) 2021-09-14

Similar Documents

Publication Publication Date Title
CN109054186A (en) A kind of Functional Polyolefine solid degradation agent
DE3885494T2 (en) Process for the preparation of propylene polymer granules.
DE10122111B4 (en) Process for the preparation of olefin polymers, as well as selected catalysts
EP1238026B1 (en) Pigment concentrates and methods for production thereof
Pehlivan et al. Characterization of pure and silver exchanged natural zeolite filled polypropylene composite films
DE60302760T2 (en) SINTERING ULTRAHOCHMOLECULAR POLYETHYLENE
DE60107928T2 (en) PROCESS FOR THE ADMINISTRATION OF ADDITIVES TO POLYMER PARTICLES
DE69304707T2 (en) METHOD FOR MODIFYING ALFA OLEFIN COPOLYMERS
JP2008248090A (en) Resin composition and filament
DE60118218T2 (en) HETEROPHASIC PROPYLENE POLYMERS WITH CONTROLLED RHEOLOGICAL VALUES
CN102358791B (en) Solid degradation agent for producing polypropylene fiber with high fusion index, and preparation method thereof
CN109233113A (en) A kind of atactic copolymerized polypropene and preparation method thereof using edman degradation Edman preparation
US2586357A (en) Tetrafluoroethylene polymer compositions
US2593582A (en) Process for producing tetrafluoroethylene polymer compositions
CA3054895C (en) Composition and method for producing composition
CN103360528A (en) Preparation method and equipment of high-performance impact polypropylene
CN107922669B (en) Polyethylene powder, process for its preparation and use for rotomoulding
EP1292644B1 (en) Pigment concentrates and method for producing them
US3012985A (en) Pelletized sulfur
CN115466449B (en) High-dispersity polyethylene primary color master batch as well as preparation method and application thereof
JP2014129614A (en) Ultrafine fiber and method for producing the same
KR20040085637A (en) Polypropylene resin having high melting tension and a process for preparing the same
CN105017597A (en) Compound additive for improving transparency of polyolefin and preparation method and application thereof
EP1322680B1 (en) Method for producing highly branched ethylene polymers
DE102006045812A1 (en) Uploaded peroxide masterbatch for targeted degradation or crosslinking reactions in plastics

Legal Events

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

Effective date of registration: 20210818

Address after: 116001 No. 51, Qiqi street, Zhongshan District, Dalian City, Liaoning Province

Applicant after: Ren Guohui

Address before: 116000 room 2001, No. 4, Shanghai Road, Zhongshan District, Dalian, Liaoning

Applicant before: DALIAN XINGHUI CHEMICAL Co.,Ltd.

TA01 Transfer of patent application right
GR01 Patent grant
GR01 Patent grant
TR01 Transfer of patent right

Effective date of registration: 20211022

Address after: No. 77-2, Baishan Road, Shahekou District, Dalian, Liaoning 116021

Patentee after: DALIAN XINGHUI CHEMICAL Co.,Ltd.

Address before: 116001 No. 51, Qiqi street, Zhongshan District, Dalian City, Liaoning Province

Patentee before: Ren Guohui

TR01 Transfer of patent right