CN108948531A - A kind of polyolefin VOC absorption master batch and preparation method thereof - Google Patents

A kind of polyolefin VOC absorption master batch and preparation method thereof Download PDF

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CN108948531A
CN108948531A CN201810791474.0A CN201810791474A CN108948531A CN 108948531 A CN108948531 A CN 108948531A CN 201810791474 A CN201810791474 A CN 201810791474A CN 108948531 A CN108948531 A CN 108948531A
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polyolefin
voc
master batch
temperature
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刘凯
伏建博
王添琪
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Anhui Jianghuai Automobile Group Corp
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Anhui Jianghuai Automobile Group Corp
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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    • 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
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    • 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
    • C08J2323/04Homopolymers or copolymers of ethene
    • C08J2323/06Polyethene
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    • 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
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    • 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
    • C08J2325/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Derivatives of such polymers
    • C08J2325/02Homopolymers or copolymers of hydrocarbons
    • C08J2325/04Homopolymers or copolymers of styrene
    • C08J2325/06Polystyrene
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2367/00Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
    • C08J2367/02Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2377/00Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
    • C08J2377/02Polyamides derived from omega-amino carboxylic acids or from lactams thereof
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K13/00Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
    • C08K13/02Organic and inorganic ingredients
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
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    • C08K3/34Silicon-containing compounds
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • C08K3/346Clay
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/13Phenols; Phenolates
    • C08K5/134Phenols containing ester groups
    • C08K5/1345Carboxylic esters of phenolcarboxylic acids
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    • 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
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    • 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

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  • 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)

Abstract

The present invention relates to a kind of polyolefin VOC absorption master batches and preparation method thereof, by weight by 40 parts -60 parts of polyolefin, 30 parts -50 parts of natural clay, 10 parts -16 parts of sodium metasilicate, 0.1 part -0.5 part of coupling agent, 0.1 part -0.3 part of erucyl amide, 0.1 part -0.5 part of antioxidant composition.This technology has synthesized a kind of VOC absorption master batch, it can improve the VOC performance of composite polyolefine material well, this tool has very important significance;And polyolefin VOC obtained adsorbs master batch simple process, cheap, has good promotional value.

Description

A kind of polyolefin VOC absorption master batch and preparation method thereof
Technical field
The invention belongs to technical field of polymer materials, a kind of polyolefin VOC absorption master batch and its preparation side are particularly related to Method.
Background technique
With the improvement of living standards, requirement of the people to material environmental protection is higher and higher, VOC performance is the one of automotive material Item important indicator.A kind of polyolefin VOC absorption master batch and preparation method thereof is made in inventor's innovation, improves present polyolefin VOC performance, this polyolefin VOC absorption master batch not yet see report so far, have very important realistic meaning.
Summary of the invention
The object of the present invention is to provide a kind of polyolefin VOC absorption master batches and preparation method thereof, to improve the VOC of polyolefin Performance.
The present invention is achieved by the following technical solutions:
A kind of polyolefin VOC absorption master batch, is made of the component of following parts by weight:
The polyolefin is in polypropylene, polyethylene, polybutylene terephthalate (PBT), polystyrene or polyamide 6 It is a kind of.
The coupling agent is carbonic ester coupling agent AC-201.
The antioxidant is three (2,4- di-t-butyl) phenyl-phosphites, four [β-(3,5- di-tert-butyl-hydroxy phenyl) Propionic acid] pentaerythritol ester or 1,3,5- trimethyls -2,4, one of 6- (3,5- di-t-butyl -4- hydroxyphenylmethyl) benzene or several The mixing of kind.
The preparation method of any of the above-described polyolefin VOC absorption master batch, comprising the following steps:
(1) 40 parts -60 parts of polyolefin, 30 parts of -50 parts of natural clays, 10 parts of -16 parts of sodium metasilicate, 0.1 part -0.5 are weighed Part coupling agent, 0.1 part of -0.3 part of erucyl amide, 0.1 part of -0.5 part of antioxidant are mixed and stirred for uniformly, obtaining mixture;
(2) by mixture obtained in step (1) from extruder extruding pelletization to get to VOC adsorb master batch.
The beneficial effects of the present invention are:
1, this technology has synthesized a kind of VOC absorption master batch, it can improve the VOC of composite polyolefine material well Can, this tool has very important significance.
2. polyolefin VOC made from this technology adsorbs master batch simple process, cheap, there is good promotional value.
Specific embodiment
Carry out the technical solution that the present invention will be described in detail by the following examples, embodiment below is merely exemplary, only It can be used to explanation and illustration technical solution of the present invention, and be not to be construed as the limitation to technical solution of the present invention.
Raw material used in present embodiments is as follows:
PBT (model 2002U), Polyplastics;PP (model T30S), Daqing petrochemical;PE (model 5070), Panjin ethylene; PA6 (model C M1017), toray;PS (model 350), state of Taiwan Province are tall;The large limited public affairs of science and technology are won in natural clay, Anhui Department;Sodium metasilicate, Xingtai Rui Xin silicon salt Manufacturing Co., Ltd;Coupling agent (model AC-201), the sincere Chemical Co., Ltd. of Nanjing Olympic;Mustard Sour amide, promote chemical products Co., Ltd in Nantong;Antioxidant (model Irganox168, Irganox1010, Irganox1330), Switzerland's Ciba.
Test equipment used in each embodiment of the application is as follows:
ZSK30 type double screw extruder, German W&P company;JL-1000 type tensile testing machine, the wide just experiment instrument in Guangzhou The production of device company;HTL900-T-5B type injection (mo(u)lding) machine, the production of Hai Tai plastics machinery Co., Ltd;XCJ-500 type shock-testing Machine, the production of Chengde testing machine factory;QT-1196 type tester for elongation, Dongguan City Gao Tai detecting instrument Co., Ltd;QD-GJS- B12K type high-speed mixer, Beijing perseverance Order instrument and meter Co., Ltd.
In the application, composite polyolefine material is polypropylene (PP), polyethylene (PE), polybutylene terephthalate (PBT) (PBT), one of polystyrene (PS), polyamide 6 (PA6).
The application provides a kind of polyolefin VOC absorption master batch, is made of the component of following parts by weight:
The coupling agent is carbonic ester coupling agent AC-201.
The antioxidant is three (2,4- di-t-butyl) phenyl-phosphites (abbreviation Irganox168), four of BASF AG [β-(3,5- di-tert-butyl-hydroxy phenyl) propionic acid] pentaerythritol ester (abbreviation Irganox1010) or 1,3,5- trimethyl -2, The mixing of one or more of 4,6- (3,5- di-t-butyl -4- hydroxyphenylmethyl) benzene (abbreviation Irganox1330).
The preparation method of any of the above-described polyolefin VOC absorption master batch, comprising the following steps:
(1) 40 parts -60 parts of polyolefin, 30 parts of -50 parts of natural clays, 10 parts of -16 parts of sodium metasilicate, 0.1 part -0.5 are weighed Part coupling agent, 0.1 part of -0.3 part of erucyl amide, 0.1 part of -0.5 part of antioxidant are mixed and stirred for uniformly, obtaining mixture;
(2) by mixture obtained in step (1) from extruder extruding pelletization to get to VOC adsorb master batch.
Embodiment 1
(1) 40 parts of PP, 30 parts of natural clays, 10 parts of sodium metasilicate, 0.1 part of coupling agent AC-201,0.1 part of erucic acid acyl are weighed Amine, 0.1 part of Irganox168 are mixed and stirred for uniformly, obtaining mixture;
(2) by mixture obtained in step (1) from extruder extruding pelletization to get to VOC adsorb master batch P1.
Wherein, double screw extruder includes six humidity provinces sequentially arranged, and area's temperature is 170 DEG C, and two area's temperature are 230 DEG C, three area's temperature are 230 DEG C, and four area's temperature are 230 DEG C, and five area's temperature are 230 DEG C, and six area's temperature are 230 DEG C, head temperature Degree is 230 DEG C, screw speed 220r/min.
Application examples 1
It takes 10 parts of P1 to be added in 90 parts of polypropylene (PP), stirs 10min through high mixer, be subsequently added into double screw extruder Middle carry out blending extrusion, obtains PP composite material X1.
Wherein, double screw extruder includes six humidity provinces sequentially arranged, and area's temperature is 170 DEG C, and two area's temperature are 230 DEG C, three area's temperature are 230 DEG C, and four area's temperature are 230 DEG C, and five area's temperature are 230 DEG C, and six area's temperature are 230 DEG C, head temperature Degree is 230 DEG C, screw speed 220r/min.
Comparative example 1
It takes in 90 parts of polypropylene (PP), stirs 10min through high mixer, be subsequently added into double screw extruder be blended and squeeze Out, PP composite material D1 is obtained.
Batten, properties of product data are made with injection molding machine in PP composite material prepared by above application examples 1 and comparative example 1 It is as shown in the table:
As can be seen from the above table: it is more preferable than the VOC performance of unmodified preceding PP that VOC absorption master batch MODIFIED PP is added.
Embodiment 2
(1) 60 parts of PBT, 50 parts of natural clays, 16 parts of sodium metasilicate, 0.5 part of coupling agent AC-201,0.3 part of erucic acid acyl are weighed Amine, 0.1 part of Irganox168,0.2 part of Irganox1010,0.2 part of Irganox1330 are mixed and stirred for uniformly, being mixed Material;
(2) by mixture obtained in step (1) from extruder extruding pelletization to get to VOC adsorb master batch P2.
Wherein, double screw extruder includes six humidity provinces sequentially arranged, and area's temperature is 200 DEG C, and two area's temperature are 260 DEG C, three area's temperature are 260 DEG C, and four area's temperature are 260 DEG C, and five area's temperature are 260 DEG C, and six area's temperature are 260 DEG C, head temperature Degree is 260 DEG C, screw speed 300r/min.
Application examples 2
It takes 20 parts of P2 to be added in 80 parts of polybutylene terephthalate (PBT)s (PBT), stirs 10min through high mixer, then Carry out blending extrusion is added twin-screw extrude, PBT composite X2 is obtained.
Wherein, double screw extruder includes six humidity provinces sequentially arranged, and area's temperature is 200 DEG C, and two area's temperature are 260 DEG C, three area's temperature are 260 DEG C, and four area's temperature are 260 DEG C, and five area's temperature are 260 DEG C, and six area's temperature are 260 DEG C, head temperature Degree is 260 DEG C, screw speed 300r/min.
Comparative example 2
It takes in 80 parts of polybutylene terephthalate (PBT)s (PBT), stirs 10min through high mixer, be subsequently added into twin-screw and squeeze Blending extrusion is carried out in machine out, obtains PBT composite D2.
Batten, properties of product number is made with injection molding machine in PBT composite prepared by above application examples 2 and comparative example 2 According to as shown in the table:
As can be seen from the above table: it is more preferable than the VOC performance of unmodified preceding PBT that VOC absorption master batch modified PBT is added.
Embodiment 3
(1) 50 parts of PE, 40 parts of natural clays, 13 parts of sodium metasilicate, 0.3 part of coupling agent AC-201,0.2 part of erucic acid acyl are weighed Amine, 0.1 part of Irganox168,0.2 part of Irganox1010 are mixed and stirred for uniformly, obtaining mixture;
(2) by mixture obtained in step (1) from extruder extruding pelletization to get to VOC adsorb master batch P3.
Wherein, double screw extruder includes six humidity provinces sequentially arranged, and area's temperature is 120 DEG C, and two area's temperature are 180 DEG C, three area's temperature are 180 DEG C, and four area's temperature are 180 DEG C, and five area's temperature are 180 DEG C, and six area's temperature are 180 DEG C, head temperature Degree is 180 DEG C, screw speed 300r/min.
Application examples 3
It takes 20 parts of P3 to be added in 80 parts of polyethylene (PE), stirs 10min through high mixer, be subsequently added into double screw extruder Middle carry out blending extrusion, obtains PE composite material X3.
Wherein, double screw extruder includes six humidity provinces sequentially arranged, and area's temperature is 120 DEG C, and two area's temperature are 180 DEG C, three area's temperature are 180 DEG C, and four area's temperature are 180 DEG C, and five area's temperature are 180 DEG C, and six area's temperature are 180 DEG C, head temperature Degree is 180 DEG C, screw speed 300r/min.
Comparative example 3
It takes in 80 parts of polyethylene (PE), stirs 10min through high mixer, be subsequently added into double screw extruder be blended and squeeze Out, PE composite material D3 is obtained.
Batten, properties of product data are made with injection molding machine in PE composite material prepared by above application examples 3 and comparative example 3 It is as shown in the table:
As can be seen from the above table: it is more preferable than the VOC performance of unmodified preceding PE that VOC absorption master batch modified PE is added.
Embodiment 4
(1) 45 parts of PA6,36 parts of natural clays, 14 parts of sodium metasilicate, 0.2 part of coupling agent AC-201,0.1 part of erucic acid acyl are weighed Amine, 0.1 part of Irganox1010,0.2 part of Irganox1330 are mixed and stirred for uniformly, obtaining mixture;
(2) by mixture obtained in step (1) from extruder extruding pelletization to get to VOC adsorb master batch P4.
Wherein, double screw extruder includes six humidity provinces sequentially arranged, and area's temperature is 230 DEG C, and two area's temperature are 260 DEG C, three area's temperature are 260 DEG C, and four area's temperature are 260 DEG C, and five area's temperature are 260 DEG C, and six area's temperature are 260 DEG C, head temperature Degree is 250 DEG C, screw speed 320r/min.
Application examples 4
It takes 20 parts of P4 to be added in 80 parts of polyamide 6s (PA6), stirs 10min through high mixer, be subsequently added into twin-screw extrusion Blending extrusion is carried out in machine, obtains PA6 composite material X4.
Wherein, double screw extruder includes six humidity provinces sequentially arranged, and area's temperature is 230 DEG C, and two area's temperature are 260 DEG C, three area's temperature are 260 DEG C, and four area's temperature are 260 DEG C, and five area's temperature are 260 DEG C, and six area's temperature are 260 DEG C, head temperature Degree is 250 DEG C, screw speed 320r/min.
Comparative example 4
It takes in 80 parts of polyamide 6s (PA6), stirs 10min through high mixer, be subsequently added into double screw extruder and be blended It squeezes out, obtains PA6 composite material D4.
Batten, properties of product number is made with injection molding machine in PA6 composite material prepared by above application examples 4 and comparative example 4 According to as shown in the table:
As can be seen from the above table: it is more preferable than the VOC performance of unmodified preceding PA6 that VOC absorption master batch modified Pa 6 is added.
Embodiment 5
(1) 44 parts of PS, 35 parts of natural clays, 11 parts of sodium metasilicate, 0.1 part of coupling agent AC-201,0.1 part of erucic acid acyl are weighed Amine, 0.1 part of Irganox1010,0.1 part of Irganox168 are mixed and stirred for uniformly, obtaining mixture;
(2) by mixture obtained in step (1) from extruder extruding pelletization to get to VOC adsorb master batch P5.
Wherein, double screw extruder includes six humidity provinces sequentially arranged, and area's temperature is 160 DEG C, and two area's temperature are 200 DEG C, three area's temperature are 200 DEG C, and four area's temperature are 200 DEG C, and five area's temperature are 200 DEG C, and six area's temperature are 200 DEG C, head temperature Degree is 200 DEG C, screw speed 280r/min.
Application examples 5
It takes 20 parts of P5 to be added in 80 parts of styrene (PS), stirs 10min through high mixer, be subsequently added into double screw extruder Middle carry out blending extrusion, obtains PS composite material X5.
Wherein, double screw extruder includes six humidity provinces sequentially arranged, and area's temperature is 160 DEG C, and two area's temperature are 200 DEG C, three area's temperature are 200 DEG C, and four area's temperature are 200 DEG C, and five area's temperature are 200 DEG C, and six area's temperature are 200 DEG C, head temperature Degree is 200 DEG C, screw speed 280r/min.
Comparative example 5
It takes in 80 parts of styrene (PS), stirs 10min through high mixer, be subsequently added into double screw extruder be blended and squeeze Out, PS composite material D5 is obtained.
Batten, properties of product data are made with injection molding machine in PS composite material prepared by above application examples 5 and comparative example 5 It is as shown in the table:
As can be seen from the above table: it is more preferable than the VOC performance of unmodified preceding PS that the modified PS of VOC absorption master batch is added.
The technical program describes a kind of polyolefin VOC absorption master batch and preparation method thereof, and polyolefine material obtained There is a degree of improvement in VOC aspect of performance, this has very heavy the application field of extension composite polyolefine material The meaning wanted.
It although an embodiment of the present invention has been shown and described, for the ordinary skill in the art, can be with A variety of variations, modification, replacement can be carried out to these embodiments without departing from the principles and spirit of the present invention by understanding And deformation, the scope of the present invention are extremely equally limited by appended claims.

Claims (5)

1. a kind of polyolefin VOC adsorbs master batch, which is characterized in that be made of the component of following parts by weight:
2. polyolefin VOC according to claim 1 adsorbs master batch, which is characterized in that the polyolefin is polypropylene, poly- second One of alkene, polybutylene terephthalate (PBT), polystyrene or polyamide 6.
3. polyolefin VOC according to claim 1 adsorbs master batch, which is characterized in that the coupling agent is carbonic ester coupling Agent AC-201.
4. polyolefin VOC according to claim 1 adsorbs master batch, which is characterized in that the antioxidant is three (2,4- bis- uncles Butyl) phenyl-phosphite, four [β-(3,5- di-tert-butyl-hydroxy phenyl) propionic acid] pentaerythritol esters or 1,3,5- trimethyls- The mixing of one or more of 2,4,6- (3,5- di-t-butyl -4- hydroxyphenylmethyl) benzene.
5. the preparation method of any one of the claims 1 to 4 polyolefin VOC absorption master batch, which is characterized in that including following Step:
(1) 40 parts -60 parts of polyolefin, 30 parts of -50 parts of natural clays, 10 parts of -16 parts of sodium metasilicate, 0.1 part of -0.5 part of idol are weighed Connection agent, 0.1 part of -0.3 part of erucyl amide, 0.1 part of -0.5 part of antioxidant are mixed and stirred for uniformly, obtaining mixture;
(2) by mixture obtained in step (1) from extruder extruding pelletization to get to VOC adsorb master batch.
CN201810791474.0A 2018-07-18 2018-07-18 A kind of polyolefin VOC absorption master batch and preparation method thereof Pending CN108948531A (en)

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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103709495A (en) * 2012-09-29 2014-04-09 青岛欣展塑胶有限公司 High-performance filling master batch used for plastics, and preparation method thereof
CN104277278A (en) * 2013-07-03 2015-01-14 合肥杰事杰新材料股份有限公司 Efficient and lasting smell removal agent master batch, and preparation method and application thereof
CN107936604A (en) * 2017-12-04 2018-04-20 王文广 One kind removes VOC masterbatch
CN108047546A (en) * 2017-10-30 2018-05-18 江苏冠恒新材料科技有限公司 A kind of smell processing master batch and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103709495A (en) * 2012-09-29 2014-04-09 青岛欣展塑胶有限公司 High-performance filling master batch used for plastics, and preparation method thereof
CN104277278A (en) * 2013-07-03 2015-01-14 合肥杰事杰新材料股份有限公司 Efficient and lasting smell removal agent master batch, and preparation method and application thereof
CN108047546A (en) * 2017-10-30 2018-05-18 江苏冠恒新材料科技有限公司 A kind of smell processing master batch and preparation method thereof
CN107936604A (en) * 2017-12-04 2018-04-20 王文广 One kind removes VOC masterbatch

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