CN108018632A - High resiliency macromolecule composite plastic seat and preparation method thereof - Google Patents
High resiliency macromolecule composite plastic seat and preparation method thereof Download PDFInfo
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- CN108018632A CN108018632A CN201711162878.5A CN201711162878A CN108018632A CN 108018632 A CN108018632 A CN 108018632A CN 201711162878 A CN201711162878 A CN 201711162878A CN 108018632 A CN108018632 A CN 108018632A
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- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D1/00—Woven fabrics designed to make specified articles
- D03D1/0017—Woven household fabrics
-
- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47G—HOUSEHOLD OR TABLE EQUIPMENT
- A47G9/00—Bed-covers; Counterpanes; Travelling rugs; Sleeping rugs; Sleeping bags; Pillows
- A47G9/02—Bed linen; Blankets; Counterpanes
- A47G9/0238—Bed linen
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/02—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from cellulose, cellulose derivatives, or proteins
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
- D01F8/06—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyolefin as constituent
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
- D01F8/10—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one other macromolecular compound obtained by reactions only involving carbon-to-carbon unsaturated bonds as constituent
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
- D01F8/16—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one other macromolecular compound obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds as constituent
-
- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D15/00—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
- D03D15/50—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads
- D03D15/56—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads elastic
-
- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D15/00—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
- D03D15/50—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads
- D03D15/58—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads characterised by the coefficients of friction
-
- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47G—HOUSEHOLD OR TABLE EQUIPMENT
- A47G9/00—Bed-covers; Counterpanes; Travelling rugs; Sleeping rugs; Sleeping bags; Pillows
- A47G2009/001—Anti-allergen; Anti-mite
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2321/00—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D10B2321/02—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polyolefins
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2401/00—Physical properties
- D10B2401/06—Load-responsive characteristics
- D10B2401/061—Load-responsive characteristics elastic
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2401/00—Physical properties
- D10B2401/06—Load-responsive characteristics
- D10B2401/063—Load-responsive characteristics high strength
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2503/00—Domestic or personal
- D10B2503/06—Bed linen
- D10B2503/062—Fitted bedsheets
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Footwear And Its Accessory, Manufacturing Method And Apparatuses (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention discloses a kind of high resiliency macromolecule composite plastic seat, including mat body, the mat body is formed by warp and weft braiding, high resiliency agent is added with the warp, the high resiliency agent includes 50 60 parts of styrene butadiene block copolymer elastomers, 20 30 parts of acrylonitrile butadient styrene elastomers, 5 10 parts of ethylene octene copolymer elastomers, 25 parts of ethylene propylene diene rubbers, 15 parts of accelerating agents, 5 10 parts of fillers by weight.The high resiliency macromolecule composite plastic seat that the present invention obtains, by being modified respectively to warp and weft, so that the macromolecule composite plastic seat has certain moisture resistance.Finally by simple, nontoxic preparation method, a kind of high resiliency macromolecule composite plastic seat with moisture resistance, wear resistance and comfort level is obtained.
Description
Technical field
The present invention relates to a kind of mat, particularly a kind of high resiliency macromolecule composite plastic seat and preparation method thereof.
Background technology
Mat is the essential product of modern life household, existing common straw mat generally using the grass processing braiding of natural seat and
Into this straw mat is not washable, easy to wear, and easily grows acarid, bacterium, and health is had an impact.At the same time with people
Raising for quality of the life, is also further enhanced for the demand of multi-functional mat.
The content of the invention
There is provided the purpose of the present invention is to solve above-mentioned the deficiencies in the prior art it is a kind of have stronger wear resistance and
High resiliency macromolecule composite plastic seat of comfort level and preparation method thereof.
To achieve these goals, a kind of high resiliency macromolecule composite plastic seat designed by the present invention, including mat sheet
Body, the mat body are formed by warp and weft braiding, and the weft is plastic tube, it includes 80-90 parts and gathers by weight
Propylene, 20-30 part polyethylene, 10-20 parts of polyolefin, 1-5 parts of anti-blushing agents, 3-5 parts of coupling agents, 2-5 parts of silicon fluorides and 1-2 parts
Modified activated carbon, wherein the modified activated carbon refers to the graphited activated carbon in part, the anti-blushing agent includes 40- by weight
50 parts of bentonites, 20-30 parts of paraffin, 10-20 parts of alkyd resins, 5-8 parts of chitosans, 2-5 parts of butenoates, 1-5 parts of Aluminates
Coupling agent, 1-5 part polyurethane based resin, 2-3 parts of calcium bicarbonates；
The warp includes 40-85 parts of viscose glue sections, 20-30 parts of spandexs, 5-10 parts of dispersants and 1-5 parts of modifications by weight
Agent, 1-5 parts of high resiliency agent, wherein modifying agent include 70 parts of opal, 20 parts of rare earth, 10 parts of diatomite by weight；The height
Elasticator (elasticizer) by weight include 50-60 parts of styrene-butadiene block copolymer elastomers, 20-30 parts of acrylonitrile-butadienes-
Styrenic copolymer elastomers, 5-10 parts of ethylene-octene copolymer elastomers, 2-5 parts of ethylene propylene diene rubbers, 1-5 parts of accelerating agents,
5-10 parts of fillers.
The invention also discloses a kind of preparation method of high resiliency macromolecule composite plastic seat, comprise the following steps：
The first step, prepares anti-blushing agent, and 40-50 parts of bentonites, 20-30 parts of paraffin, 10-20 parts of alkyd resins, 5-8 parts of shells are gathered
Sugar, 2-5 parts of butenoates, 1-5 parts of aluminate coupling agents, 1-5 parts of polyurethane based resins, 2-3 parts of calcium bicarbonates are uniformly mixed, and
The agitating and heating 2h in 300-400 DEG C, grind into powder is up to anti-blushing agent after cooling；
Second step, prepares weft, first by normal activated carbon in nitrogen protection, 1200-2000 DEG C of roasting 10-24 h, to carry out
For graphitization processing so as to obtain modified activated carbon, the graphitization component content wherein in modified activated carbon accounts for the 20- of its gross mass
40%, then by 80-90 parts of polypropylene, 20-30 parts of polyethylene, 10-20 parts of polyolefin, 1-5 parts of anti-blushing agents, 3-5 parts of coupling agents,
2-5 parts of silicon fluorides and 1-2 parts of modified activated carbons are uniformly mixed, at 200-220 DEG C after double-screw extruding pelletizing, wire drawing
To weft；
3rd step, prepares high resiliency agent, by 50-60 parts of styrene-butadiene block copolymer elastomers, 20-30 parts of acrylonitrile-
Butadiene-styrene copolymer elastomer, 5-10 parts of ethylene-octene copolymer elastomers, 2-5 parts of ethylene propylene diene rubbers, 1-5 parts
Accelerating agent, 5-10 a part filler are uniformly mixed, in 200 DEG C of heating reaction 30min, up to high resiliency agent after cooling；
4th step, prepares warp, first by ball milling after 70 parts of opal, 20 parts of rare earth, the mixing of 10 parts of diatomite disperse 1 it is small when obtain
Modifying agent, then by 40-85 parts of viscose glue sections, 20-30 parts of spandexs, 5-10 parts of dispersants and 1-5 parts of modifying agent, 1-5 parts it is high-elastic
Property agent is uniformly mixed, and warp is obtained after double-screw extruding pelletizing, wire drawing at 250-300 DEG C；
5th step, prepares high resiliency macromolecule composite plastic seat, above-mentioned warp and weft is woven on braider
Obtain high resiliency macromolecule composite plastic seat.
The weft is to mix polypropylene, polyethylene, polyolefin, can take the advantages of respective, so as to improve
The intensity of weft, wear-resistant and moisture resistance.
Bentonite, paraffin, calcium bicarbonate are inorganic anti-blushing agents in the anti-blushing agent, alkyd resin, chitosan, butenoic acid
Ester is efficient organic anti-blushing agent, and above-mentioned inorganic anti-blushing agent and organic anti-blushing agent can be bound up by aluminate coupling agent,
And the lifting of dampproof effect is improved by polyurethane based resin, there is collaboration between above-mentioned inorganic anti-blushing agent and organic anti-blushing agent
Effect, further functions as moisture-proof effect.
The coupling agent is used to be coupled polypropylene, polyethylene, polyolefin, and the silicon fluoride is then used for improving the stretching of weft
Intensity.The modified activated carbon refers to the graphited activated carbon in part, and graphitization component content accounts for the 20-40% of its gross mass, institute
Carrier can be used as by stating graphited activated carbon, using the electron transfer characteristic of graphite-structure, improve in anti-blushing agent it is effective into
Divide and played, strengthen dampproof effect.
The warp is mixed to prepare by viscose glue section and spandex, and wherein viscose rayon has good hygroscopicity, has light
Slide the characteristics such as nice and cool, ventilative, antistatic, dyeing is gorgeous.Spandex fibre has a high resiliency, high restorative, have it is preferable it is acidproof,
The property such as alkaline-resisting, fast light.Dispersant and modifying agent are added, for improving the characteristic of warp, is particularly diatom in the modifying agent
Soil be used as carrier so that opal and rare earth can be adsorbed in diatomaceous surface volume, and opal and rare earth then conduct bear from
Sub- powder is used to discharge anion., can be with the water such as the sweat of skin surface when the direct skin contact of negative ion powder and human body
Divide reaction, so as to accelerate the release of anion.Negative ion powder can penetrate blood-brain barrier and enter cerebrospinal fluid, adjust cerebral cortex work(
Can, excited and depression is tended to balance.By reconciling the level of human body endorphin pituitary and interferon, calm, town is played
Pain acts on.
High resiliency agent in the warp, with styrene-butadiene block copolymer elastomer, acrylonitrile-butadiene-benzene
Toughening Effect of Ethylene Copolymer Elastomer, ethylene-octene copolymer elastomer are bulk elastomer, are coordinated with ethylene propylene diene rubber and accelerating agent
To provide elasticity, so that a variety of elastomers can play a role jointly, it is final to improve overall elasticity.
High resiliency macromolecule composite plastic seat that the present invention obtains, by being modified respectively to warp and weft, from
And cause the macromolecule composite plastic seat that there is certain moisture resistance.Finally by simple, nontoxic preparation method, obtain a kind of
High resiliency macromolecule composite plastic seat with moisture resistance, wear resistance and comfort level.
Embodiment
With reference to embodiment, the present invention is further described.
Embodiment 1：
A kind of high resiliency macromolecule composite plastic seat provided in this embodiment, including mat body, the mat body is by warp
Formed with weft braiding, the weft is plastic tube, it includes 80 parts of polypropylene, 20 parts of polyethylene, 10 parts of polyenes by weight
Hydrocarbon, 1 part of anti-blushing agent, 3 parts of coupling agents, 2 parts of silicon fluorides and 1 part of modified activated carbon, wherein the modified activated carbon refers to part
Graphited activated carbon, the anti-blushing agent include 40 parts of bentonites, 20 parts of paraffin, 10 parts of alkyd resins, 5 parts of shells and gather by weight
Sugar, 2 parts of butenoates, 1 part of aluminate coupling agent, 1 part of polyurethane based resin, 2 parts of calcium bicarbonates；
The warp includes 40 parts of viscose glue sections, 20 parts of spandexs, 5 parts of dispersants and 1 part of modifying agent, 1 part of high resiliency by weight
Agent, wherein modifying agent include 70 parts of opal, 20 parts of rare earth, 10 parts of diatomite by weight；The high resiliency agent is by weight
Including 50 parts of styrene-butadiene block copolymer elastomers, 20 parts of acrylonitrile-butadiene-styrene copolymer elastomers, 5
Part ethylene-octene copolymer elastomer, 2 parts of ethylene propylene diene rubbers, 1 part of accelerating agent, 5 parts of fillers.
The invention also discloses a kind of preparation method of high resiliency macromolecule composite plastic seat, comprise the following steps：
The first step, prepares anti-blushing agent, by 40 parts of bentonites, 20 parts of paraffin, 10 parts of alkyd resins, 5 parts of chitosans, 2 parts of butenoic acids
Ester, 1 part of aluminate coupling agent, 1 part of polyurethane based resin, 2 parts of calcium bicarbonates are uniformly mixed, and stirring adds in 300-400 DEG C
Hot 2h, grind into powder is up to anti-blushing agent after cooling；
Second step, prepares weft, first by normal activated carbon in nitrogen protection, 1200-2000 DEG C of roasting 10-24 h, to carry out
For graphitization processing so as to obtain modified activated carbon, the graphitization component content wherein in modified activated carbon accounts for the 20- of its gross mass
40%, then by 80 parts of polypropylene, 20 parts of polyethylene, 10 parts of polyolefin, 1 part of anti-blushing agent, 3 parts of coupling agents, 2 parts of silicon fluorides and 1
Part modified activated carbon is uniformly mixed, and weft is obtained after double-screw extruding pelletizing, wire drawing at 200-220 DEG C；
3rd step, prepares high resiliency agent, and 50 parts of styrene-butadiene block copolymer elastomers, 20 parts of acrylonitrile-butadienes-
Styrenic copolymer elastomers, 5 parts of ethylene-octene copolymer elastomers, 2 parts of ethylene propylene diene rubbers, 1 part of accelerating agent, 5 parts of fillers
It is uniformly mixed, in 200 DEG C of heating reaction 30min, up to high resiliency agent after cooling；
4th step, prepares warp, first by ball milling after 70 parts of opal, 20 parts of rare earth, the mixing of 10 parts of diatomite disperse 1 it is small when obtain
40 parts of viscose glue sections, 20 parts of spandexs, 5 parts of dispersants and 1 part of modifying agent, 1 part of high resiliency agent, are then uniformly mixed by modifying agent,
At 250-300 DEG C warp is obtained after double-screw extruding pelletizing, wire drawing；
5th step, prepares high resiliency macromolecule composite plastic seat, above-mentioned warp and weft is woven on braider
Obtain high resiliency macromolecule composite plastic seat.
High resiliency macromolecule composite plastic seat made from the present embodiment, can absorb external pressure in the range of 10cm,
And peripheral distortion is not affected, and the noiseless generation during pressing energetically.
Embodiment 2：
High resiliency macromolecule composite plastic seat provided in this embodiment, its raw material and preparation method are substantially identical with embodiment 1, its
The main distinction is, in the present embodiment, the weft by weight include 90 parts of polypropylene, 30 parts of polyethylene, 20 parts of polyolefin,
5 parts of anti-blushing agents, 5 parts of coupling agents, 5 parts of silicon fluorides and 2 parts of modified activated carbons.
High resiliency macromolecule composite plastic seat made from the present embodiment, can absorb external pressure in the range of 10cm,
And peripheral distortion is not affected, and the noiseless generation during pressing energetically.
Embodiment 3：
High resiliency macromolecule composite plastic seat provided in this embodiment, its raw material and preparation method are substantially identical with embodiment 1, its
The main distinction is, in the present embodiment, the anti-blushing agent includes 50 parts of bentonites, 30 parts of paraffin, 20 parts of alkyd trees by weight
Fat, 8 parts of chitosans, 5 parts of butenoates, 5 parts of aluminate coupling agents, 5 parts of polyurethane based resins, 3 parts of calcium bicarbonates.
High resiliency macromolecule composite plastic seat made from the present embodiment, can absorb external pressure in the range of 10cm,
And peripheral distortion is not affected, and the noiseless generation during pressing energetically.
Embodiment 4：
High resiliency macromolecule composite plastic seat provided in this embodiment, its raw material and preparation method are substantially identical with embodiment 1, its
The main distinction is, in the present embodiment, the warp includes 85 parts of viscose glue sections, 30 parts of spandexs, 10 parts of dispersants by weight
With 5 parts of modifying agent, 5 parts of high resiliency agent, wherein modifying agent includes 70 parts of opal, 20 parts of rare earth, 10 parts of diatomite by weight.
High resiliency macromolecule composite plastic seat made from the present embodiment, can absorb external pressure in the range of 10cm,
And peripheral distortion is not affected, and the noiseless generation during pressing energetically.
Embodiment 5：
High resiliency macromolecule composite plastic seat provided in this embodiment, its raw material and preparation method are substantially identical with embodiment 1, its
The main distinction is, in the present embodiment, the high resiliency agent includes 60 parts of styrene-butadiene block copolymer bullets by weight
Property body, 30 parts of acrylonitrile-butadiene-styrene copolymer elastomers, 10 parts of ethylene-octene copolymer elastomers, 5 parts of ternary second
Third rubber, 5 parts of accelerating agents, 10 parts of fillers.
High resiliency macromolecule composite plastic seat made from the present embodiment, can absorb external pressure in the range of 10cm,
And peripheral distortion is not affected, and the noiseless generation during pressing energetically.
Claims (2)
1. a kind of high resiliency macromolecule composite plastic seat, including mat body, it is characterised in that：The mat body by warp and
Weft braiding forms, and the weft is plastic tube, it includes 80-90 parts of polypropylene, 20-30 parts of polyethylene, 10-20 by weight
Part polyolefin, 1-5 parts of anti-blushing agents, 3-5 parts of coupling agents, 2-5 parts of silicon fluorides and 1-2 parts of modified activated carbons, wherein the modification
Activated carbon refers to the graphited activated carbon in part, the anti-blushing agent include by weight 40-50 parts of bentonites, 20-30 parts of paraffin,
10-20 parts of alkyd resins, 5-8 parts of chitosans, 2-5 parts of butenoates, 1-5 parts of aluminate coupling agents, 1-5 parts of polyurethanes trees
Fat, 2-3 part calcium bicarbonate；
The warp includes 40-85 parts of viscose glue sections, 20-30 parts of spandexs, 5-10 parts of dispersants and 1-5 parts of modifications by weight
Agent, 1-5 parts of high resiliency agent, wherein modifying agent include 70 parts of opal, 20 parts of rare earth, 10 parts of diatomite by weight；The height
Elasticator (elasticizer) by weight include 50-60 parts of styrene-butadiene block copolymer elastomers, 20-30 parts of acrylonitrile-butadienes-
Styrenic copolymer elastomers, 5-10 parts of ethylene-octene copolymer elastomers, 2-5 parts of ethylene propylene diene rubbers, 1-5 parts of accelerating agents,
5-10 parts of fillers.
A kind of 2. preparation method of high resiliency macromolecule composite plastic seat as claimed in claim 1, it is characterised in that including with
Lower step：
The first step, prepares anti-blushing agent, and 40-50 parts of bentonites, 20-30 parts of paraffin, 10-20 parts of alkyd resins, 5-8 parts of shells are gathered
Sugar, 2-5 parts of butenoates, 1-5 parts of aluminate coupling agents, 1-5 parts of polyurethane based resins, 2-3 parts of calcium bicarbonates are uniformly mixed, and
The agitating and heating 2h in 300-400 DEG C, grind into powder is up to anti-blushing agent after cooling；
Second step, prepares weft, first by normal activated carbon in nitrogen protection, 1200-2000 DEG C of roasting 10-24 h, to carry out
For graphitization processing so as to obtain modified activated carbon, the graphitization component content wherein in modified activated carbon accounts for the 20- of its gross mass
40%, then by 80-90 parts of polypropylene, 20-30 parts of polyethylene, 10-20 parts of polyolefin, 1-5 parts of anti-blushing agents, 3-5 parts of coupling agents,
2-5 parts of silicon fluorides and 1-2 parts of modified activated carbons are uniformly mixed, at 200-220 DEG C after double-screw extruding pelletizing, wire drawing
To weft；
3rd step, prepares high resiliency agent, by 50-60 parts of styrene-butadiene block copolymer elastomers, 20-30 parts of acrylonitrile-
Butadiene-styrene copolymer elastomer, 5-10 parts of ethylene-octene copolymer elastomers, 2-5 parts of ethylene propylene diene rubbers, 1-5 parts
Accelerating agent, 5-10 a part filler are uniformly mixed, in 200 DEG C of heating reaction 30min, up to high resiliency agent after cooling；
4th step, prepares warp, first by ball milling after 70 parts of opal, 20 parts of rare earth, the mixing of 10 parts of diatomite disperse 1 it is small when obtain
Modifying agent, then by 40-85 parts of viscose glue sections, 20-30 parts of spandexs, 5-10 parts of dispersants and 1-5 parts of modifying agent, 1-5 parts it is high-elastic
Property agent is uniformly mixed, and warp is obtained after double-screw extruding pelletizing, wire drawing at 250-300 DEG C；
5th step, prepares high resiliency macromolecule composite plastic seat, above-mentioned warp and weft is woven on braider
Obtain high resiliency macromolecule composite plastic seat.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201711162878.5A CN108018632A (en) | 2017-11-21 | 2017-11-21 | High resiliency macromolecule composite plastic seat and preparation method thereof |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201711162878.5A CN108018632A (en) | 2017-11-21 | 2017-11-21 | High resiliency macromolecule composite plastic seat and preparation method thereof |
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| CN108018632A true CN108018632A (en) | 2018-05-11 |
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| CN201711162878.5A Withdrawn CN108018632A (en) | 2017-11-21 | 2017-11-21 | High resiliency macromolecule composite plastic seat and preparation method thereof |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115124024A (en) * | 2022-08-04 | 2022-09-30 | 安徽固瑞特新材料科技有限公司 | Porous carbon material, composite rubber filler, preparation method of composite rubber filler and rubber material |
-
2017
- 2017-11-21 CN CN201711162878.5A patent/CN108018632A/en not_active Withdrawn
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| 肖长发等: "《化学纤维概论》", 31 July 2005, 中国纺织出版社 * |
| 蔡再生: "《纤维化学与物理》", 31 October 2005, 中国纺织出版社 * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115124024A (en) * | 2022-08-04 | 2022-09-30 | 安徽固瑞特新材料科技有限公司 | Porous carbon material, composite rubber filler, preparation method of composite rubber filler and rubber material |
| CN115124024B (en) * | 2022-08-04 | 2024-04-12 | 安徽固瑞特新材料科技有限公司 | Porous carbon material, composite rubber filler, preparation method of porous carbon material and composite rubber filler, and rubber material |
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