CN105504778A - Automotive interior material with high rigidity and hardness - Google Patents
Automotive interior material with high rigidity and hardness Download PDFInfo
- Publication number
- CN105504778A CN105504778A CN201610055294.7A CN201610055294A CN105504778A CN 105504778 A CN105504778 A CN 105504778A CN 201610055294 A CN201610055294 A CN 201610055294A CN 105504778 A CN105504778 A CN 105504778A
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- Prior art keywords
- parts
- deionized water
- automotive interior
- aqueous polyurethane
- interior material
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- Pending
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- 239000000463 material Substances 0.000 title claims abstract description 32
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 23
- 239000004814 polyurethane Substances 0.000 claims abstract description 22
- 239000000835 fiber Substances 0.000 claims abstract description 21
- 229920002635 polyurethane Polymers 0.000 claims abstract description 21
- 210000002268 wool Anatomy 0.000 claims abstract description 21
- 239000008367 deionised water Substances 0.000 claims abstract description 16
- 229910021641 deionized water Inorganic materials 0.000 claims abstract description 16
- 229920001661 Chitosan Polymers 0.000 claims abstract description 14
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000004927 clay Substances 0.000 claims abstract description 10
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000006004 Quartz sand Substances 0.000 claims abstract description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229920002472 Starch Polymers 0.000 claims abstract description 8
- 239000008107 starch Substances 0.000 claims abstract description 8
- 235000019698 starch Nutrition 0.000 claims abstract description 8
- 238000000034 method Methods 0.000 claims abstract description 7
- 230000008569 process Effects 0.000 claims abstract description 7
- 239000004408 titanium dioxide Substances 0.000 claims abstract description 7
- 229910052602 gypsum Inorganic materials 0.000 claims abstract description 5
- 239000010440 gypsum Substances 0.000 claims abstract description 5
- 239000000243 solution Substances 0.000 claims description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 12
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 6
- 239000000839 emulsion Substances 0.000 claims description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 6
- 239000011259 mixed solution Substances 0.000 claims description 6
- -1 polyoxyethylene Polymers 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 5
- 239000002994 raw material Substances 0.000 claims description 4
- 238000005266 casting Methods 0.000 claims description 3
- 238000005238 degreasing Methods 0.000 claims description 3
- 230000001877 deodorizing effect Effects 0.000 claims description 3
- 238000007598 dipping method Methods 0.000 claims description 3
- 239000006185 dispersion Substances 0.000 claims description 3
- 238000001704 evaporation Methods 0.000 claims description 3
- 230000008020 evaporation Effects 0.000 claims description 3
- 238000001914 filtration Methods 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 238000003760 magnetic stirring Methods 0.000 claims description 3
- 230000007935 neutral effect Effects 0.000 claims description 3
- 235000011837 pasties Nutrition 0.000 claims description 3
- 238000005453 pelletization Methods 0.000 claims description 3
- 238000003756 stirring Methods 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 2
- 239000002202 Polyethylene glycol Substances 0.000 abstract 1
- 235000019864 coconut oil Nutrition 0.000 abstract 1
- 239000003240 coconut oil Substances 0.000 abstract 1
- XRWMGCFJVKDVMD-UHFFFAOYSA-M didodecyl(dimethyl)azanium;bromide Chemical compound [Br-].CCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCC XRWMGCFJVKDVMD-UHFFFAOYSA-M 0.000 abstract 1
- 229920001223 polyethylene glycol Polymers 0.000 abstract 1
- 230000008901 benefit Effects 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000003245 working effect Effects 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 238000004500 asepsis Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000002649 leather substitute Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- ZWYDDDAMNQQZHD-UHFFFAOYSA-L titanium(ii) chloride Chemical compound [Cl-].[Cl-].[Ti+2] ZWYDDDAMNQQZHD-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/46—Oxides or hydroxides of elements of Groups 4 or 14 of the Periodic Table; Titanates; Zirconates; Stannates; Plumbates
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/01—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
- D06M15/03—Polysaccharides or derivatives thereof
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/53—Polyethers
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/08—Stabilised against heat, light or radiation or oxydation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/14—Polymer mixtures characterised by other features containing polymeric additives characterised by shape
- C08L2205/16—Fibres; Fibrils
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/02—Natural fibres, other than mineral fibres
- D06M2101/10—Animal fibres
- D06M2101/12—Keratin fibres or silk
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Textile Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Artificial Filaments (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Vehicle Interior And Exterior Ornaments, Soundproofing, And Insulation (AREA)
Abstract
The invention discloses an automotive interior material with high rigidity and hardness. The automotive interior material is prepared from, by weight, 25-30 parts of wool fiber, 4-5 parts of chitosan, 2-3 parts of titanium dioxide, 0.6-1 part of polyethylene glycol, 100-110 parts of waterborne polyurethane, 0.2-0.4 part of didodecyldimethylammonium bromide, 5-6 parts of clay, 3-4 parts of coconut oil, 3-4 parts of starch, 6-7 parts of quartz sand, 5-6 parts of copper nitrate, 4-5 parts of gypsum and a proper amount of deionized water. The preparing process is simple, rigidity and hardness are high, and the automotive interior material is high in safety and environment friendliness, long in service life and worth popularization.
Description
Technical field
The present invention relates to technical field of polymer materials, particularly relate to the automotive interior material that a kind of rigidity strong hardness is high.
Background technology
Along with the develop rapidly of automobile industry, human consumer not only just values the attractive in appearance of automobile external moulding when purchasing car, attractive in appearance to automotive interior material of increasing human consumer, functional, low emission is had higher requirement, and automotive interior material has become the important factor affecting vehicle complete vehicle quality and class.Current automotive trim material has PVC imitation leather, PU leatheroid etc.For the material of automotive trim, good property indices should be had, such as, resistance to illumination, low-temperature resistant flexile are fire-retardant good, low fogging, requirement simultaneously need meet the requirement to raw-material composition of laws and regulations, and requires that the recyclable ratio proposing inside gadget is more and more higher.But now conventional automotive interior material exists problem more or less, can not meet the requirement of consuming public to interior material, along with the proposition of energy-saving, emission-reducing, environment friendly slogan, therefore, the automotive interior material researching and developing novel environment friendly recoverable is necessary.
Polyurethane material is applied to many fields because of the structure of its uniqueness and excellent performance, it is the focus of research always, and water-base polyurethane material has low cost because of it, pollution-free, the advantage such as flexible, have broad application prospects, the synthetic leather processed with urethane and leatheroid have good advantage, as intensity is high, wear resistance is good, flexible resistance is good, lower temperature resistance and oil resistant, chemical resistance is good, but shortcoming is that the water tolerance of aqueous polyurethane and thermotolerance are not high, water vapour permeability is poor, have a strong impact on work-ing life and the human comfort of material, reduce the performance of automobile, the present invention focuses on the improvement of this respect, to reaching the requirement of people to material for car interior trim parts.
Summary of the invention
The object of the invention is exactly the defect in order to make up prior art, provides the automotive interior material that a kind of rigidity strong hardness is high.
The present invention is achieved by the following technical solutions:
The automotive interior material that rigidity strong hardness is high, is made up of the raw material of following weight part: wool fiber 25-30, chitosan 4-5, titanium dioxide 2-3, polyoxyethylene glycol 0.6-1, aqueous polyurethane 100-110, didodecyldimethylammbromide bromide 0.2-0.4, clay 5-6, Oleum Cocois 3-4, starch 3-4, quartz sand 6-7, cupric nitrate 5-6, gypsum 4-5, deionized water are appropriate;
The automotive interior material that described a kind of rigidity strong hardness is high, be made up of following concrete preparation method:
(1) wool fiber is carried out degreasing deodorizing process, again mechanical disintegration is carried out to it, obtain median size lower than the wool fiber of 10 μm, again chitosan is dissolved the chitosan solution obtaining 8-10% with 5% acetum, then by titanium dioxide and polyoxyethylene glycol mixing 4-5 times amount deionized water ultrasonic disperse even, add above-mentioned chitosan solution and continue dispersion 5-10min, finally wool fiber is impregnated in mixed solution, dipping 10-20min;
(2) wool fiber is transferred in high-temperature high-pressure reaction kettle together with mixed solution, constant temperature process 0.5-1h under 100-120 ° of C, clarify to solution with deionized water wash after modified wool is taken out, finally naturally dry for subsequent use;
(3) Oleum Cocois, starch, quartz sand and deionized water are mixed, heated and stirred forms pasty state, add aqueous polyurethane rapid stirring 1-2h again, by the dissolve with ethanol of didodecyldimethylammbromide bromide by 3-4 times amount, clay is added to ultrasonic disperse 10-20min in didodecyldimethylammbromide bromide solution again, filtration deionized water wash is to neutral post-drying;
(4) clay and modified aqueous polyurethane emulsion are added in magnetic stirring apparatus, heating evaporation 1-2h in water bath with thermostatic control, then by modified aqueous polyurethane emulsion casting film-forming, drying for standby at the temperature of 60-90 ° of C;
(5) modified aqueous polyurethane step (4) obtained and other surplus materialss are added in twin screw extruder, spout adds modified woolen fiber prepared by step (2), at the temperature of 100-110 ° of C, screw speed is extruding pelletization under the condition of 150 revs/min, obtains material of the present invention.
Advantage of the present invention is: the present invention adopts water-base polyurethane material as automotive interior material, asepsis environment-protecting, be harmful to human health, and adopt the hardness of starch and quartz sand enhancing modified aqueous polyurethane, intensity and anti-impact force, extend its work-ing life, and by chitosan and titanium dichloride load on wool fiber, strengthen it antibacterial, uvioresistant, automatically cleaning and shrinkproof effect, the wool fiber of modification is added in urethane when not affecting its mechanical property and thermostability and enhances water vapour permeability, improve human comfort and easily clean, the copper sulfate added and gypsum coordinate the physical strength that can greatly improve material, thermotolerance and dimensional stability, preparation technology of the present invention is simple, rigidity is strong, hardness is high, as automotive interior material, there is good Safety and Environmental Protection, long service life, be worthy to be popularized.
Embodiment
The automotive interior material that rigidity strong hardness is high, is made up of the raw material of following weight part (kilogram): wool fiber 25, chitosan 4, titanium dioxide 2, polyoxyethylene glycol 0.6, aqueous polyurethane 100, didodecyldimethylammbromide bromide 0.2, clay 5, Oleum Cocois 3, starch 3, quartz sand 6, cupric nitrate 5, gypsum 4, deionized water are appropriate;
The automotive interior material that described a kind of rigidity strong hardness is high, be made up of following concrete preparation method:
(1) wool fiber is carried out degreasing deodorizing process, again mechanical disintegration is carried out to it, obtain median size lower than the wool fiber of 10 μm, again chitosan is dissolved the chitosan solution obtaining 8% with 5% acetum, then titanium dioxide and polyoxyethylene glycol are mixed even with 4 times amount deionized water ultrasonic disperse, add above-mentioned chitosan solution and continue dispersion 5min, finally wool fiber is impregnated in mixed solution, dipping 10min;
(2) wool fiber is transferred in high-temperature high-pressure reaction kettle together with mixed solution, constant temperature process 0.5h under 100 ° of C, clarify to solution with deionized water wash after modified wool is taken out, finally naturally dry for subsequent use;
(3) Oleum Cocois, starch, quartz sand and deionized water are mixed, heated and stirred forms pasty state, add aqueous polyurethane rapid stirring 1h again, by the dissolve with ethanol of didodecyldimethylammbromide bromide by 3 times amount, clay is added to ultrasonic disperse 10min in didodecyldimethylammbromide bromide solution again, filtration deionized water wash is to neutral post-drying;
(4) clay and modified aqueous polyurethane emulsion are added in magnetic stirring apparatus, heating evaporation 1h in water bath with thermostatic control, then by modified aqueous polyurethane emulsion casting film-forming, drying for standby at the temperature of 60 ° of C;
(5) modified aqueous polyurethane step (4) obtained and other surplus materialss are added in twin screw extruder, spout adds modified woolen fiber prepared by step (2), at the temperature of 100 ° of C, screw speed is extruding pelletization under the condition of 150 revs/min, obtains material of the present invention.
Performance test:
Test its material according to embodiment preparation, result is as follows: water vapour permeability: 3675g/ (m2 ﹡ 24h), water-intake rate: 5.2%, tension set: 594%, tensile strength: 148Mpa, ageing resistance: 4 grades, light fastness aging: 4 grades, rolling processing: good.
Claims (2)
1. the automotive interior material that a rigidity strong hardness is high, it is characterized in that, be made up of the raw material of following weight part: wool fiber 25-30, chitosan 4-5, titanium dioxide 2-3, polyoxyethylene glycol 0.6-1, aqueous polyurethane 100-110, didodecyldimethylammbromide bromide 0.2-0.4, clay 5-6, Oleum Cocois 3-4, starch 3-4, quartz sand 6-7, cupric nitrate 5-6, gypsum 4-5, deionized water are appropriate.
2. the automotive interior material that a kind of rigidity strong hardness is high according to claim 1, is characterized in that, is made up of following concrete preparation method:
(1) wool fiber is carried out degreasing deodorizing process, again mechanical disintegration is carried out to it, obtain median size lower than the wool fiber of 10 μm, again chitosan is dissolved the chitosan solution obtaining 8-10% with 5% acetum, then by titanium dioxide and polyoxyethylene glycol mixing 4-5 times amount deionized water ultrasonic disperse even, add above-mentioned chitosan solution and continue dispersion 5-10min, finally wool fiber is impregnated in mixed solution, dipping 10-20min;
(2) wool fiber is transferred in high-temperature high-pressure reaction kettle together with mixed solution, constant temperature process 0.5-1h under 100-120 ° of C, clarify to solution with deionized water wash after modified wool is taken out, finally naturally dry for subsequent use;
(3) Oleum Cocois, starch, quartz sand and deionized water are mixed, heated and stirred forms pasty state, add aqueous polyurethane rapid stirring 1-2h again, by the dissolve with ethanol of didodecyldimethylammbromide bromide by 3-4 times amount, clay is added to ultrasonic disperse 10-20min in didodecyldimethylammbromide bromide solution again, filtration deionized water wash is to neutral post-drying;
(4) clay and modified aqueous polyurethane emulsion are added in magnetic stirring apparatus, heating evaporation 1-2h in water bath with thermostatic control, then by modified aqueous polyurethane emulsion casting film-forming, drying for standby at the temperature of 60-90 ° of C;
(5) modified aqueous polyurethane step (4) obtained and other surplus materialss are added in twin screw extruder, spout adds modified woolen fiber prepared by step (2), at the temperature of 100-110 ° of C, screw speed is extruding pelletization under the condition of 150 revs/min, obtains material of the present invention.
Priority Applications (1)
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CN201610055294.7A CN105504778A (en) | 2016-01-26 | 2016-01-26 | Automotive interior material with high rigidity and hardness |
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CN201610055294.7A CN105504778A (en) | 2016-01-26 | 2016-01-26 | Automotive interior material with high rigidity and hardness |
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101798466A (en) * | 2010-03-16 | 2010-08-11 | 龙海市奈特化工有限责任公司 | Natural fiber composite material and preparation method thereof |
CN102912634A (en) * | 2012-10-18 | 2013-02-06 | 西安工程大学 | Method for modifying surfaces of wool fibers by using tetrabutyl titanate and chitosan |
CN104479334A (en) * | 2014-10-23 | 2015-04-01 | 合肥金伶俐服饰有限公司 | Skin-imitated polyurethane interior trim leather and producing method thereof |
CN105176028A (en) * | 2015-09-23 | 2015-12-23 | 芜湖环瑞汽车内饰件有限公司 | Ultraviolet and aging resisting composite material for automotive upholstery and a preparing method composite material |
-
2016
- 2016-01-26 CN CN201610055294.7A patent/CN105504778A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101798466A (en) * | 2010-03-16 | 2010-08-11 | 龙海市奈特化工有限责任公司 | Natural fiber composite material and preparation method thereof |
CN102912634A (en) * | 2012-10-18 | 2013-02-06 | 西安工程大学 | Method for modifying surfaces of wool fibers by using tetrabutyl titanate and chitosan |
CN104479334A (en) * | 2014-10-23 | 2015-04-01 | 合肥金伶俐服饰有限公司 | Skin-imitated polyurethane interior trim leather and producing method thereof |
CN105176028A (en) * | 2015-09-23 | 2015-12-23 | 芜湖环瑞汽车内饰件有限公司 | Ultraviolet and aging resisting composite material for automotive upholstery and a preparing method composite material |
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