CN116444893A - High-strength wear-resistant polypropylene composite material - Google Patents
High-strength wear-resistant polypropylene composite material Download PDFInfo
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- CN116444893A CN116444893A CN202310349769.3A CN202310349769A CN116444893A CN 116444893 A CN116444893 A CN 116444893A CN 202310349769 A CN202310349769 A CN 202310349769A CN 116444893 A CN116444893 A CN 116444893A
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- carbon fiber
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- silicon carbide
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- 239000004743 Polypropylene Substances 0.000 title claims abstract description 64
- -1 polypropylene Polymers 0.000 title claims abstract description 63
- 229920001155 polypropylene Polymers 0.000 title claims abstract description 63
- 239000002131 composite material Substances 0.000 title claims abstract description 32
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims abstract description 83
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims abstract description 38
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 27
- 239000000945 filler Substances 0.000 claims abstract description 27
- 229910052588 hydroxylapatite Inorganic materials 0.000 claims abstract description 22
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 claims abstract description 22
- 229910000029 sodium carbonate Inorganic materials 0.000 claims abstract description 19
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 59
- 239000004917 carbon fiber Substances 0.000 claims description 59
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 57
- 238000002156 mixing Methods 0.000 claims description 48
- 239000000463 material Substances 0.000 claims description 45
- 238000006243 chemical reaction Methods 0.000 claims description 42
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 39
- 238000003756 stirring Methods 0.000 claims description 39
- 238000001035 drying Methods 0.000 claims description 38
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 38
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 31
- 238000005406 washing Methods 0.000 claims description 29
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 27
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 26
- 239000003365 glass fiber Substances 0.000 claims description 25
- 239000003963 antioxidant agent Substances 0.000 claims description 22
- 230000003078 antioxidant effect Effects 0.000 claims description 22
- 239000004611 light stabiliser Substances 0.000 claims description 22
- 239000000314 lubricant Substances 0.000 claims description 22
- 239000006087 Silane Coupling Agent Substances 0.000 claims description 19
- 229910021389 graphene Inorganic materials 0.000 claims description 18
- 238000001132 ultrasonic dispersion Methods 0.000 claims description 18
- 229910021589 Copper(I) bromide Inorganic materials 0.000 claims description 17
- NKNDPYCGAZPOFS-UHFFFAOYSA-M copper(i) bromide Chemical compound Br[Cu] NKNDPYCGAZPOFS-UHFFFAOYSA-M 0.000 claims description 17
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 16
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 16
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 16
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 16
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 16
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 claims description 16
- 229910052802 copper Inorganic materials 0.000 claims description 16
- 239000010949 copper Substances 0.000 claims description 16
- 239000008367 deionised water Substances 0.000 claims description 16
- 229910021641 deionized water Inorganic materials 0.000 claims description 16
- 239000003792 electrolyte Substances 0.000 claims description 16
- 238000002360 preparation method Methods 0.000 claims description 16
- 239000004014 plasticizer Substances 0.000 claims description 15
- 238000001291 vacuum drying Methods 0.000 claims description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
- 238000000151 deposition Methods 0.000 claims description 14
- 230000008021 deposition Effects 0.000 claims description 14
- 238000001914 filtration Methods 0.000 claims description 14
- 230000010355 oscillation Effects 0.000 claims description 14
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical group [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 11
- 239000011575 calcium Substances 0.000 claims description 11
- 229910052791 calcium Inorganic materials 0.000 claims description 11
- 238000005245 sintering Methods 0.000 claims description 11
- 238000001652 electrophoretic deposition Methods 0.000 claims description 10
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims description 10
- YOCIJWAHRAJQFT-UHFFFAOYSA-N 2-bromo-2-methylpropanoyl bromide Chemical compound CC(C)(Br)C(Br)=O YOCIJWAHRAJQFT-UHFFFAOYSA-N 0.000 claims description 9
- 238000002844 melting Methods 0.000 claims description 9
- 230000008018 melting Effects 0.000 claims description 9
- 239000002070 nanowire Substances 0.000 claims description 9
- 229910052786 argon Inorganic materials 0.000 claims description 8
- 238000004140 cleaning Methods 0.000 claims description 8
- 238000001816 cooling Methods 0.000 claims description 8
- 238000004090 dissolution Methods 0.000 claims description 8
- 235000019441 ethanol Nutrition 0.000 claims description 8
- 238000000227 grinding Methods 0.000 claims description 8
- 238000007873 sieving Methods 0.000 claims description 8
- 239000000377 silicon dioxide Substances 0.000 claims description 8
- 235000012239 silicon dioxide Nutrition 0.000 claims description 8
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical group NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 7
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 7
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical group [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims description 7
- 235000013539 calcium stearate Nutrition 0.000 claims description 7
- 239000008116 calcium stearate Substances 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 239000005457 ice water Substances 0.000 claims description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical compound CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 claims description 7
- 239000002994 raw material Substances 0.000 claims description 7
- 238000002791 soaking Methods 0.000 claims description 7
- JMTMSDXUXJISAY-UHFFFAOYSA-N 2H-benzotriazol-4-ol Chemical group OC1=CC=CC2=C1N=NN2 JMTMSDXUXJISAY-UHFFFAOYSA-N 0.000 claims description 6
- NPZTUJOABDZTLV-UHFFFAOYSA-N hydroxybenzotriazole Substances O=C1C=CC=C2NNN=C12 NPZTUJOABDZTLV-UHFFFAOYSA-N 0.000 claims description 6
- 238000000034 method Methods 0.000 abstract description 10
- 230000008569 process Effects 0.000 abstract description 9
- 238000013461 design Methods 0.000 abstract description 3
- 230000000052 comparative effect Effects 0.000 description 21
- 238000005299 abrasion Methods 0.000 description 9
- 239000011159 matrix material Substances 0.000 description 7
- 238000004132 cross linking Methods 0.000 description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 4
- 229910001424 calcium ion Inorganic materials 0.000 description 4
- 230000006872 improvement Effects 0.000 description 4
- YIXJRHPUWRPCBB-UHFFFAOYSA-N magnesium nitrate Chemical compound [Mg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O YIXJRHPUWRPCBB-UHFFFAOYSA-N 0.000 description 4
- 230000002087 whitening effect Effects 0.000 description 4
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 238000010382 chemical cross-linking Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 101710141544 Allatotropin-related peptide Proteins 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000010560 atom transfer radical polymerization reaction Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 230000021523 carboxylation Effects 0.000 description 1
- 238000006473 carboxylation reaction Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000011895 specific detection Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/06—Elements
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/06—Pretreated ingredients and ingredients covered by the main groups C08K3/00 - C08K7/00
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/38—Boron-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/14—Glass
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/02—Ingredients treated with inorganic substances
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/04—Ingredients treated with organic substances
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/04—Ingredients treated with organic substances
- C08K9/06—Ingredients treated with organic substances with silicon-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/10—Encapsulated ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-containing compounds
- C08K2003/321—Phosphates
- C08K2003/325—Calcium, strontium or barium phosphate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Abstract
The invention discloses a high-strength wear-resistant polypropylene composite material, which comprises components such as polypropylene, modified carbon fiber, hydroxyapatite, an antiwear agent, sodium carbonate, modified filler and the like. The process is reasonable in design, proper in component proportion, and the prepared polypropylene has higher strength, wear resistance and excellent mechanical property, can be applied to a plurality of fields, and is higher in practicability.
Description
Technical Field
The invention relates to the technical field of polypropylene materials, in particular to a high-strength wear-resistant polypropylene composite material.
Background
Polypropylene, also called PP, is a colorless, odorless, nontoxic and semitransparent solid substance, is also a thermoplastic synthetic resin with excellent performance, is colorless and semitransparent thermoplastic light-weight general-purpose plastic, has chemical resistance, heat resistance, electrical insulation, high-strength mechanical property, good high-wear-resistance processing property and the like, and can be applied to various fields.
Most of the polypropylene materials on the market at present have excellent mechanical properties, but in practical application, we find that in some environments with higher strength requirements, the strength of polypropylene still cannot meet the requirements of us, and the polypropylene has poor wear resistance and inconvenience in practical application.
In order to solve the problem, we disclose a high-strength wear-resistant polypropylene composite material and a preparation method thereof.
Disclosure of Invention
The invention aims to provide a high-strength wear-resistant polypropylene composite material and a preparation method thereof, so as to solve the problems in the background technology.
In order to solve the technical problems, the invention provides the following technical scheme:
a high-strength wear-resistant polypropylene composite material is characterized in that: the polypropylene composite material comprises the following raw materials in parts by weight: 90-100 parts of polypropylene, 10-15 parts of modified carbon fiber, 5-8 parts of hydroxyapatite, 0.5-1 part of antioxidant, 2-3 parts of plasticizer, 2-3 parts of lubricant, 3-4 parts of light stabilizer, 5-7 parts of wear-resistant agent, 10-12 parts of sodium carbonate and 10-15 parts of modified filler.
The modified carbon fiber is prepared by modifying the surface of the pretreated carbon fiber by a silane coupling agent; the pretreated carbon fiber is a carbon fiber with graphene oxide deposited on the surface.
In a more optimized scheme, the modified filler is carboxylated silicon carbide and glass fiber, and the mass ratio of the carboxylated silicon carbide to the glass fiber is 1:1.
more optimized scheme, the lubricant is calcium stearate; the antioxidant is p-phenylenediamine.
In a more optimized scheme, the light stabilizer is any one of hydroxybenzophenone and hydroxybenzotriazole.
In an optimized scheme, the wear-resistant agent is a calcium hexaboride nanowire.
The optimized scheme is that the preparation method of the high-strength wear-resistant polypropylene composite material comprises the following steps:
(1) Preparing materials;
(2) Mixing carbon powder and silicon dioxide, adding an ethanol solution for dissolution, ultrasonic dispersion, vacuum drying, vacuum sintering in an argon environment, cooling along with a furnace, grinding and crushing, and sieving with a 50-mesh sieve to obtain silicon carbide powder;
(3) Mixing graphene oxide and a calcium nitrate solution, stirring, adding an isopropanol solution, and performing ultrasonic dispersion to obtain an electrolyte;
taking carbon fiber as a negative electrode, taking a copper sheet as a positive electrode, placing the copper sheet in electrolyte for electrophoretic deposition, taking out the carbon fiber, ultrasonically cleaning with deionized water, and drying to obtain pretreated carbon fiber;
mixing and stirring pretreated carbon fibers and absolute ethyl alcohol, performing ultrasonic dispersion, adding a silane coupling agent, performing ultrasonic dispersion, reacting in a water bath at 65-75 ℃, washing and drying to obtain modified carbon fibers;
(4) Placing silicon carbide powder into N-methyl pyrrolidone solution, placing in ice water bath, adding 2-bromo isobutyryl bromide under nitrogen environment, heating to 60-65deg.C, stirring for reaction, washing with anhydrous ethanol, and vacuum drying to obtain material A;
taking a material A, cuprous bromide and glycidyl methacrylate, carrying out oscillation reaction in a closed environment at a reaction temperature of 30-35 ℃, placing the materials in a water bath at 60-65 ℃ after the reaction, standing, centrifugally filtering, washing and drying to obtain a material B;
taking a material B, cuprous bromide, methyl acrylate and pentamethyl diethylenetriamine, carrying out oscillation reaction in a closed environment at a reaction temperature of 30-35 ℃, standing, centrifugally filtering, washing, drying, and then soaking in a sodium hydroxide solution for 20-22 hours to obtain carboxylated silicon carbide;
(5) And dissolving polypropylene, modified carbon fiber and hydroxyapatite in deionized water, mixing and stirring, adding carboxylated silicon carbide, glass fiber and sodium carbonate solution, stirring for reaction, adding an antioxidant, a plasticizer, a light stabilizer, a lubricant and an antiwear agent, uniformly mixing, drying, putting into a double-screw extruder, melting and mixing, and extruding to obtain a finished product.
The more optimized scheme comprises the following steps:
(1) Preparing materials;
(2) Mixing carbon powder and silicon dioxide, adding ethanol solution for dissolution, performing ultrasonic dispersion for 1-2h, performing vacuum drying at 70-80 ℃, performing vacuum sintering in an argon environment, cooling along with a furnace, grinding, crushing, and sieving with a 50-mesh sieve to obtain silicon carbide powder;
(3) Mixing graphene oxide and a calcium nitrate solution, stirring for 10-20min, adding an isopropanol solution, and performing ultrasonic dispersion for 1-2h to obtain an electrolyte;
taking carbon fiber as a negative electrode, taking a copper sheet as a positive electrode, placing the copper sheet in electrolyte for electrophoretic deposition, wherein the deposition voltage is 120-160V, the deposition time is 1-2min, taking out the carbon fiber, ultrasonically cleaning the carbon fiber with deionized water for 5-10min, and drying the carbon fiber for 20-24h to obtain pretreated carbon fiber;
mixing and stirring the pretreated carbon fiber and absolute ethyl alcohol for 10-20min, ultrasonically dispersing for 30-40min, adding a silane coupling agent, ultrasonically dispersing for 20-30min, reacting for 5-6h in a water bath at 65-75 ℃, washing and drying to obtain modified carbon fiber;
(4) Placing silicon carbide powder into N-methyl pyrrolidone solution, placing in ice water bath, adding 2-bromo isobutyryl bromide under nitrogen environment, heating to 60-65deg.C, stirring for reacting for 18-20 hr, washing with anhydrous ethanol, and vacuum drying to obtain material A;
taking a material A, cuprous bromide and glycidyl methacrylate, carrying out oscillation reaction for 1-1.2h in a closed environment, wherein the reaction temperature is 30-35 ℃, placing in a water bath at 60-65 ℃ after the reaction, standing for 20-24h, centrifugally filtering, washing and drying to obtain a material B;
taking a material B, cuprous bromide, methyl acrylate and pentamethyldiethylenetriamine, carrying out oscillation reaction for 1-1.5h in a closed environment, standing for 20-24h at a reaction temperature of 30-35 ℃, centrifugally filtering, washing, drying, and soaking in a sodium hydroxide solution for 20-22h to obtain carboxylated silicon carbide;
(5) Dissolving polypropylene, modified carbon fiber and hydroxyapatite in deionized water, mixing and stirring for 10-20min, adding carboxylated silicon carbide, glass fiber and sodium carbonate solution, stirring and reacting for 20-30min, adding antioxidant, plasticizer, light stabilizer, lubricant and antiwear agent, mixing uniformly, drying, placing in a double screw extruder, melting and mixing, and extruding to obtain the final product.
In the more optimized scheme, in the step (3), the silane coupling agent is KH550.
In the step (2), the sintering temperature is 1400-1500 ℃ and the sintering time is 2.5-3h.
Compared with the prior art, the invention has the following beneficial effects:
the application discloses a high-strength wear-resistant polypropylene composite material and a preparation method thereof, wherein the high-strength wear-resistant polypropylene composite material comprises components such as polypropylene, modified carbon fiber, hydroxyapatite, an antiwear agent, sodium carbonate, modified filler and the like, the modified carbon fiber is added, during preparation, graphene oxide is deposited on the surface of the carbon fiber through electrophoretic deposition, the pretreated carbon fiber is prepared, during preparation of the pretreated fiber, a calcium nitrate solution is added during electrophoretic deposition, graphene oxide nanoparticles adsorb calcium ions to be positively charged, under the action of an electric field, the graphene oxide is deposited on the surface of the carbon fiber through the charge adsorption effect to form a wrapping layer, due to the existence of the graphene oxide, the roughness of the surface of the carbon fiber is greatly increased, the contact area between the carbon fiber and a polypropylene matrix is greatly increased, and the surface of the graphene oxide contains a large number of active groups which can be in hydrogen bond and chemical crosslinking with polypropylene, so that the interface performance between the pretreated carbon fiber and the polypropylene is further improved, and the mechanical property of the composite material is improved.
The pretreatment carbon fiber is subjected to surface silane coupling agent improvement, the silane coupling agent is KH550, KH550 is amino functional silane, the pretreatment carbon fiber is modified by the silane coupling agent to introduce amino, the existence of the amino can further improve the crosslinking between the pretreatment carbon fiber and the polypropylene, and meanwhile, the modified filler contains a large amount of carboxyl groups, and the crosslinking exists between the modified filler and the carbon fiber, so that the crosslinking is intertangled and entangled in the polypropylene resin matrix, and the strength of the composite material is further improved.
The modified filler is introduced, the modified filler comprises carboxylated silicon carbide and glass fibers, the silicon carbide and the glass fibers have excellent mechanical properties, and the modified filler is used as the filler to be introduced into a polypropylene matrix, so that the strength of the composite material can be effectively improved; meanwhile, during preparation, the method carries out surface carboxylation modification on silicon carbide, takes 2-bromoisobutyryl bromide as an initiator, and takes bromine element on carbonyl group and hydroxyl group on the surface of the silicon carbide to react to generate ester, so that bromine element is introduced into the silicon carbide, and then takes ATRP reaction to initiate methyl acrylate polymerization reaction on the surface of the silicon carbide, and acrylic acid is generated after hydrolysis in sodium hydroxide solution, so that carboxyl is introduced; the existence of carboxyl can effectively improve the crosslinking between the silicon carbide filler and the polypropylene matrix and between the silicon carbide filler and the graphene oxide, and the silicon carbide filler and the polypropylene matrix and the graphene oxide cooperate to improve the mechanical property of the composite material.
However, in the process, the ester generated by the reaction of the hydroxyl group on the surface of the silicon carbide and the 2-bromoisobutyryl bromide is hydrolyzed when the subsequent sodium hydroxide solution is soaked, so that the grafting condition of carboxyl is affected.
In the preparation process of the polypropylene composite material, hydroxyapatite is also introduced, and the hydroxyapatite can be used as filler for reinforcement, and can also be subjected to hydrogen bonding and chemical crosslinking with modified carbon fiber and modified filler to improve the crosslinking density and strength of the matrix; meanwhile, in the subsequent preparation process, calcium ions can be released by the hydroxyapatite, calcium ions are adsorbed on the surface of the graphene oxide, the calcium ions can react with carbonate ions to generate amorphous calcium carbonate, and carboxyl groups on the surface of silicon carbide can also react with carbonate ions, so that the silicon carbide, the graphene oxide and the hydroxyapatite are physically crosslinked through the calcium carbonate, and the mechanical property of the polypropylene composite material is further improved.
In the application, the wear-resistant agent is selected as the calcium hexaboride nanowire, and the calcium hexaboride has the excellent properties of low density, high melting point, high hardness, high chemical stability and the like, and the calcium hexaboride is introduced into the polypropylene material as the wear-resistant agent, so that the wear resistance and the strength of the polypropylene composite material can be effectively improved. Meanwhile, the calcium hexaboride nanowire structure can be mutually crosslinked and wound with carbon fibers and glass fibers, so that the crosslinking strength of a matrix is improved.
The application discloses a high-strength wear-resistant polypropylene composite material and a preparation method thereof, wherein the process design is reasonable, the component proportion is proper, and the prepared polypropylene has higher strength and wear resistance, excellent mechanical property, can be applied to a plurality of fields and has higher practicability.
Detailed Description
The following description of the technical solutions in the embodiments of the present invention will be clear and complete, and it is obvious that the described embodiments are only some embodiments of the present invention, but not all embodiments. All other embodiments, which can be made by those skilled in the art based on the embodiments of the invention without making any inventive effort, are intended to be within the scope of the invention.
Example 1:
a preparation method of a high-strength wear-resistant polypropylene composite material comprises the following steps:
(1) Preparing materials;
(2) Mixing carbon powder and silicon dioxide, adding ethanol solution for dissolution, performing ultrasonic dispersion for 1h, performing vacuum drying at 70 ℃, performing vacuum sintering in an argon environment at 1400 ℃ for 3h, cooling with a furnace, grinding and crushing, and sieving with a 50-mesh sieve to obtain silicon carbide powder;
(3) Mixing graphene oxide and a calcium nitrate solution, stirring for 10min, adding an isopropanol solution, and performing ultrasonic dispersion for 1h to obtain an electrolyte;
taking carbon fiber as a negative electrode, taking a copper sheet as a positive electrode, placing the copper sheet in electrolyte for electrophoretic deposition, wherein the deposition voltage is 120V, the deposition time is 1min, taking out the carbon fiber, ultrasonically cleaning with deionized water for 5min, and drying for 20h to obtain pretreated carbon fiber;
mixing and stirring the pretreated carbon fiber and absolute ethyl alcohol for 10min, ultrasonically dispersing for 30min, adding a silane coupling agent, ultrasonically dispersing for 20min, reacting for 6h in a water bath at 65 ℃, washing and drying to obtain modified carbon fiber; wherein the silane coupling agent is KH550;
(4) Placing silicon carbide powder into N-methyl pyrrolidone solution, placing in ice water bath, adding 2-bromo isobutyryl bromide under nitrogen environment, heating to 60 ℃, stirring for reacting for 20h, washing with absolute ethyl alcohol, and vacuum drying to obtain a material A;
taking a material A, cuprous bromide and glycidyl methacrylate, carrying out oscillation reaction for 1h in a closed environment at the reaction temperature of 35 ℃, placing the mixture in a water bath at 60 ℃ after the reaction, standing for 20h, centrifugally filtering, washing and drying to obtain a material B;
taking a material B, cuprous bromide, methyl acrylate and pentamethyl diethylenetriamine, carrying out oscillation reaction for 1h in a closed environment, standing for 24h at a reaction temperature of 30 ℃, centrifugally filtering, washing, drying, and soaking in a sodium hydroxide solution for 20h to obtain carboxylated silicon carbide;
(5) Dissolving polypropylene, modified carbon fiber and hydroxyapatite in deionized water, mixing and stirring for 10min, adding carboxylated silicon carbide, glass fiber and sodium carbonate solution, stirring and reacting for 20min, adding antioxidant, plasticizer, light stabilizer, lubricant and wear-resisting agent, uniformly mixing, drying, placing in a double-screw extruder, melting and mixing, and extruding to obtain the finished product.
In this embodiment, the polypropylene composite material comprises the following raw materials: 90 parts of polypropylene, 10 parts of modified carbon fiber, 5 parts of hydroxyapatite, 0.5 part of antioxidant, 2 parts of plasticizer, 2 parts of lubricant, 3 parts of light stabilizer, 5 parts of wear-resistant agent, 10 parts of sodium carbonate and 10 parts of modified filler.
The modified filler is carboxylated silicon carbide and glass fiber, and the mass ratio of the carboxylated silicon carbide to the glass fiber is 1:1. the lubricant is calcium stearate; the antioxidant is p-phenylenediamine. The light stabilizer is hydroxybenzophenone. The wear-resistant agent is a calcium hexaboride nanowire.
Example 2:
a preparation method of a high-strength wear-resistant polypropylene composite material comprises the following steps:
(1) Preparing materials;
(2) Mixing carbon powder and silicon dioxide, adding ethanol solution for dissolution, performing ultrasonic dispersion for 1.5h, performing vacuum drying at 75 ℃, performing vacuum sintering in an argon environment at 1450 ℃ for 2.8h, cooling with a furnace, grinding and crushing, and sieving with a 50-mesh sieve to obtain silicon carbide powder;
(3) Mixing graphene oxide and a calcium nitrate solution, stirring for 15min, adding an isopropanol solution, and performing ultrasonic dispersion for 1.5h to obtain an electrolyte;
taking carbon fiber as a negative electrode, taking a copper sheet as a positive electrode, placing the copper sheet in electrolyte for electrophoretic deposition, wherein the deposition voltage is 145V, the deposition time is 1.5min, taking out the carbon fiber, ultrasonically cleaning the carbon fiber with deionized water for 8min, and drying the carbon fiber for 22h to obtain pretreated carbon fiber;
mixing and stirring the pretreated carbon fiber and absolute ethyl alcohol for 15min, ultrasonically dispersing for 35min, adding a silane coupling agent, ultrasonically dispersing for 25min, reacting for 5.5h in a water bath at 70 ℃, washing and drying to obtain modified carbon fiber; wherein the silane coupling agent is KH550;
(4) Placing silicon carbide powder into N-methyl pyrrolidone solution, placing in ice water bath, adding 2-bromo isobutyryl bromide under nitrogen environment, heating to 63 ℃, stirring for reaction for 19h, washing with absolute ethyl alcohol, and vacuum drying to obtain a material A;
taking a material A, cuprous bromide and glycidyl methacrylate, carrying out oscillation reaction for 1.1h in a closed environment, wherein the reaction temperature is 32 ℃, placing the material A, cuprous bromide and glycidyl methacrylate in a water bath at 63 ℃ after the reaction, standing for 22h, centrifugally filtering, washing and drying to obtain a material B;
taking a material B, cuprous bromide, methyl acrylate and pentamethyl diethylenetriamine, carrying out oscillation reaction for 1.3 hours in a closed environment, standing for 22 hours at the reaction temperature of 32 ℃, centrifugally filtering, washing, drying, and then soaking in a sodium hydroxide solution for 21 hours to obtain carboxylated silicon carbide;
(5) Dissolving polypropylene, modified carbon fiber and hydroxyapatite in deionized water, mixing and stirring for 15min, adding carboxylated silicon carbide, glass fiber and sodium carbonate solution, stirring and reacting for 25min, adding antioxidant, plasticizer, light stabilizer, lubricant and wear-resisting agent, uniformly mixing, drying, placing in a double-screw extruder, melting and mixing, and extruding to obtain the finished product.
In this embodiment, the polypropylene composite material comprises the following raw materials: 95 parts of polypropylene, 12 parts of modified carbon fiber, 6 parts of hydroxyapatite, 0.8 part of antioxidant, 2.5 parts of plasticizer, 2.5 parts of lubricant, 3.5 parts of light stabilizer, 6 parts of wear-resistant agent, 11 parts of sodium carbonate and 13 parts of modified filler.
The modified filler is carboxylated silicon carbide and glass fiber, and the mass ratio of the carboxylated silicon carbide to the glass fiber is 1:1. the lubricant is calcium stearate; the antioxidant is p-phenylenediamine. The light stabilizer is hydroxybenzotriazole. The wear-resistant agent is a calcium hexaboride nanowire.
Example 3:
a preparation method of a high-strength wear-resistant polypropylene composite material comprises the following steps:
(1) Preparing materials;
(2) Mixing carbon powder and silicon dioxide, adding ethanol solution for dissolution, performing ultrasonic dispersion for 2 hours, performing vacuum drying at 80 ℃, performing vacuum sintering in an argon environment at a sintering temperature of 1500 ℃ for 2.5 hours, cooling with a furnace, grinding and crushing, and sieving with a 50-mesh sieve to obtain silicon carbide powder;
(3) Mixing graphene oxide and a calcium nitrate solution, stirring for 20min, adding an isopropanol solution, and performing ultrasonic dispersion for 2h to obtain an electrolyte;
taking carbon fiber as a negative electrode, taking a copper sheet as a positive electrode, placing the copper sheet in electrolyte for electrophoretic deposition, wherein the deposition voltage is 160V, the deposition time is 1min, taking out the carbon fiber, ultrasonically cleaning the carbon fiber with deionized water for 10min, and drying the carbon fiber for 20h to obtain pretreated carbon fiber;
mixing and stirring the pretreated carbon fiber and absolute ethyl alcohol for 20min, ultrasonically dispersing for 40min, adding a silane coupling agent, ultrasonically dispersing for 30min, reacting for 6h in a water bath at 65 ℃, washing and drying to obtain modified carbon fiber; wherein the silane coupling agent is KH550;
(4) Placing silicon carbide powder into N-methyl pyrrolidone solution, placing in ice water bath, adding 2-bromo isobutyryl bromide under nitrogen environment, heating to 65deg.C, stirring for reacting for 18h, washing with anhydrous ethanol, and vacuum drying to obtain material A;
taking a material A, cuprous bromide and glycidyl methacrylate, carrying out oscillation reaction for 1.2 hours in a closed environment, wherein the reaction temperature is 35 ℃, placing the materials in a water bath at 65 ℃ after the reaction, standing for 24 hours, centrifugally filtering, washing and drying to obtain a material B;
taking a material B, cuprous bromide, methyl acrylate and pentamethyl diethylenetriamine, carrying out oscillation reaction for 1.5h in a closed environment, standing for 24h at a reaction temperature of 30 ℃, centrifugally filtering, washing, drying, and soaking in a sodium hydroxide solution for 22h to obtain carboxylated silicon carbide;
(5) Dissolving polypropylene, modified carbon fiber and hydroxyapatite in deionized water, mixing and stirring for 20min, adding carboxylated silicon carbide, glass fiber and sodium carbonate solution, stirring and reacting for 30min, adding antioxidant, plasticizer, light stabilizer, lubricant and wear-resisting agent, uniformly mixing, drying, placing in a double-screw extruder, melting and mixing, and extruding to obtain the finished product.
In this embodiment, the polypropylene composite material comprises the following raw materials: 100 parts of polypropylene, 15 parts of modified carbon fiber, 8 parts of hydroxyapatite, 1 part of antioxidant, 3 parts of plasticizer, 3 parts of lubricant, 4 parts of light stabilizer, 7 parts of wear-resistant agent, 12 parts of sodium carbonate and 15 parts of modified filler.
The modified filler is carboxylated silicon carbide and glass fiber, and the mass ratio of the carboxylated silicon carbide to the glass fiber is 1:1. the lubricant is calcium stearate; the antioxidant is p-phenylenediamine. The light stabilizer is hydroxybenzotriazole. The wear-resistant agent is a calcium hexaboride nanowire.
Comparative example 1: comparative example 1 was modified on the basis of example 2, no antiwear agent was added in comparative example 1, and other process parameters and component contents were identical to those of example 2.
Comparative example 2: comparative example 2 was modified on the basis of example 2, no sodium carbonate was added in comparative example 2, and other process parameters and component contents were identical to those of example 2.
Comparative example 3: comparative example 3 was modified on the basis of example 2, and sodium carbonate and hydroxyapatite were not added in comparative example 3, and other process parameters and component contents were identical to those of example 2.
Comparative example 4: comparative example 4 the improvement was made on the basis of example 2, and silicon carbide powder was added in comparative example 4, and other process parameters and component contents were identical to those of example 2.
A preparation method of a high-strength wear-resistant polypropylene composite material comprises the following steps:
(1) Preparing materials;
(2) Mixing carbon powder and silicon dioxide, adding ethanol solution for dissolution, performing ultrasonic dispersion for 1.5h, performing vacuum drying at 75 ℃, performing vacuum sintering in an argon environment at 1450 ℃ for 2.8h, cooling with a furnace, grinding and crushing, and sieving with a 50-mesh sieve to obtain silicon carbide powder;
(3) Mixing graphene oxide and a calcium nitrate solution, stirring for 15min, adding an isopropanol solution, and performing ultrasonic dispersion for 1.5h to obtain an electrolyte;
taking carbon fiber as a negative electrode, taking a copper sheet as a positive electrode, placing the copper sheet in electrolyte for electrophoretic deposition, wherein the deposition voltage is 145V, the deposition time is 1.5min, taking out the carbon fiber, ultrasonically cleaning the carbon fiber with deionized water for 8min, and drying the carbon fiber for 22h to obtain pretreated carbon fiber;
mixing and stirring the pretreated carbon fiber and absolute ethyl alcohol for 15min, ultrasonically dispersing for 35min, adding a silane coupling agent, ultrasonically dispersing for 25min, reacting for 5.5h in a water bath at 70 ℃, washing and drying to obtain modified carbon fiber; wherein the silane coupling agent is KH550;
(4) Dissolving polypropylene, modified carbon fiber and hydroxyapatite in deionized water, mixing and stirring for 15min, adding silicon carbide powder, glass fiber and sodium carbonate solution, stirring and reacting for 25min, adding antioxidant, plasticizer, light stabilizer, lubricant and antiwear agent, mixing uniformly, drying, placing in a double screw extruder, melting and mixing, and extruding to obtain the final product.
In this embodiment, the polypropylene composite material comprises the following raw materials: 95 parts of polypropylene, 12 parts of modified carbon fiber, 6 parts of hydroxyapatite, 0.8 part of antioxidant, 2.5 parts of plasticizer, 2.5 parts of lubricant, 3.5 parts of light stabilizer, 6 parts of wear-resistant agent, 11 parts of sodium carbonate and 13 parts of modified filler.
The modified filler is silicon carbide powder and glass fiber, and the mass ratio of the silicon carbide powder to the glass fiber is 1:1. the lubricant is calcium stearate; the antioxidant is p-phenylenediamine. The light stabilizer is hydroxybenzotriazole. The wear-resistant agent is a calcium hexaboride nanowire.
Comparative example 5: comparative example 5 the improvement was made on the basis of example 2, and a magnesium nitrate solution was added to comparative example 5, and other process parameters and component contents were identical to those of example 2.
A preparation method of a high-strength wear-resistant polypropylene composite material comprises the following steps:
(1) Preparing materials;
(2) Mixing carbon powder and silicon dioxide, adding ethanol solution for dissolution, performing ultrasonic dispersion for 1.5h, performing vacuum drying at 75 ℃, performing vacuum sintering in an argon environment at 1450 ℃ for 2.8h, cooling with a furnace, grinding and crushing, and sieving with a 50-mesh sieve to obtain silicon carbide powder;
(3) Mixing graphene oxide and magnesium nitrate solution, stirring for 15min, adding isopropanol solution, and performing ultrasonic dispersion for 1.5h to obtain electrolyte;
taking carbon fiber as a negative electrode, taking a copper sheet as a positive electrode, placing the copper sheet in electrolyte for electrophoretic deposition, wherein the deposition voltage is 145V, the deposition time is 1.5min, taking out the carbon fiber, ultrasonically cleaning the carbon fiber with deionized water for 8min, and drying the carbon fiber for 22h to obtain pretreated carbon fiber;
mixing and stirring the pretreated carbon fiber and absolute ethyl alcohol for 15min, ultrasonically dispersing for 35min, adding a silane coupling agent, ultrasonically dispersing for 25min, reacting for 5.5h in a water bath at 70 ℃, washing and drying to obtain modified carbon fiber; wherein the silane coupling agent is KH550;
(4) Placing silicon carbide powder into N-methyl pyrrolidone solution, placing in ice water bath, adding 2-bromo isobutyryl bromide under nitrogen environment, heating to 63 ℃, stirring for reaction for 19h, washing with absolute ethyl alcohol, and vacuum drying to obtain a material A;
taking a material A, cuprous bromide and glycidyl methacrylate, carrying out oscillation reaction for 1.1h in a closed environment, wherein the reaction temperature is 32 ℃, placing the material A, cuprous bromide and glycidyl methacrylate in a water bath at 63 ℃ after the reaction, standing for 22h, centrifugally filtering, washing and drying to obtain a material B;
taking a material B, cuprous bromide, methyl acrylate and pentamethyl diethylenetriamine, carrying out oscillation reaction for 1.3 hours in a closed environment, standing for 22 hours at the reaction temperature of 32 ℃, centrifugally filtering, washing, drying, and then soaking in a sodium hydroxide solution for 21 hours to obtain carboxylated silicon carbide;
(5) Dissolving polypropylene, modified carbon fiber and hydroxyapatite in deionized water, mixing and stirring for 15min, adding carboxylated silicon carbide, glass fiber and sodium carbonate solution, stirring and reacting for 25min, adding antioxidant, plasticizer, light stabilizer, lubricant and wear-resisting agent, uniformly mixing, drying, placing in a double-screw extruder, melting and mixing, and extruding to obtain the finished product.
In this embodiment, the polypropylene composite material comprises the following raw materials: 95 parts of polypropylene, 12 parts of modified carbon fiber, 6 parts of hydroxyapatite, 0.8 part of antioxidant, 2.5 parts of plasticizer, 2.5 parts of lubricant, 3.5 parts of light stabilizer, 6 parts of wear-resistant agent, 11 parts of sodium carbonate and 13 parts of modified filler.
The modified filler is carboxylated silicon carbide and glass fiber, and the mass ratio of the carboxylated silicon carbide to the glass fiber is 1:1. the lubricant is calcium stearate; the antioxidant is p-phenylenediamine. The light stabilizer is hydroxybenzotriazole. The wear-resistant agent is a calcium hexaboride nanowire.
Detection test:
1. the polypropylene prepared in examples 1 to 3 and comparative examples 1 to 5 was processed into a sheet, and the tensile strength and elongation at break thereof were measured according to GB/T1040-1992 test method for tensile Property of Plastic, respectively.
2. Wear resistance: a sample plate of 150 x 100 x 3.2mm was formed, see test method SAE J948:2003, load 500 g/wheel at test, and observe the abrasion condition of the material surface after 350 revolutions.
Specific detection data are as follows:
| project | Example 1 | Example 2 | Example 3 | Comparative example 1 |
| Tensile Strength (MPa) | 19.8 | 20.4 | 20.8 | 18.8 |
| Elongation at break (%) | 346 | 357 | 351 | 332 |
| Wear resistance | No abrasion mark and whitening | No abrasion mark and whitening | No abrasion mark and whitening | Slight abrasion mark and blushing |
| Project | Comparative example 2 | Comparative example 3 | Comparative example 4 | Comparative example 5 |
| Tensile Strength (MPa) | 16.4 | 15.8 | 17.2 | 19.3 |
| Elongation at break (%) | 289 | 271 | 291 | 338 |
| Wear resistance | Slight abrasion mark and blushing | Slight abrasion mark and blushing | Slight abrasion mark and blushing | No abrasion mark and whitening |
Conclusion: the process is reasonable in design, proper in component proportion, and the prepared polypropylene has higher strength, wear resistance and excellent mechanical property, can be applied to a plurality of fields, and is higher in practicability.
Finally, it should be noted that: the foregoing description is only a preferred embodiment of the present invention, and the present invention is not limited thereto, but it is to be understood that modifications and equivalents of some of the technical features described in the foregoing embodiments may be made by those skilled in the art, although the present invention has been described in detail with reference to the foregoing embodiments. Any modification, equivalent replacement, improvement, etc. made within the spirit and principle of the present invention should be included in the protection scope of the present invention.
Claims (1)
1. A high-strength wear-resistant polypropylene composite material is characterized in that: the polypropylene composite material comprises the following raw materials in parts by weight: 95 parts of polypropylene, 12 parts of modified carbon fiber, 6 parts of hydroxyapatite, 0.8 part of antioxidant, 2.5 parts of plasticizer, 2.5 parts of lubricant, 3.5 parts of light stabilizer, 6 parts of wear-resistant agent, 11 parts of sodium carbonate and 13 parts of modified filler;
the modified filler is carboxylated silicon carbide and glass fiber, and the mass ratio of the carboxylated silicon carbide to the glass fiber is 1:1, a step of; the lubricant is calcium stearate; the antioxidant is p-phenylenediamine, the light stabilizer is hydroxybenzotriazole, and the wear-resistant agent is a calcium hexaboride nanowire;
the preparation method of the polypropylene composite material comprises the following steps:
(1) Preparing materials;
(2) Mixing carbon powder and silicon dioxide, adding ethanol solution for dissolution, performing ultrasonic dispersion for 1.5h, performing vacuum drying at 75 ℃, performing vacuum sintering in an argon environment at 1450 ℃ for 2.8h, cooling with a furnace, grinding and crushing, and sieving with a 50-mesh sieve to obtain silicon carbide powder;
(3) Mixing graphene oxide and a calcium nitrate solution, stirring for 15min, adding an isopropanol solution, and performing ultrasonic dispersion for 1.5h to obtain an electrolyte;
taking carbon fiber as a negative electrode, taking a copper sheet as a positive electrode, placing the copper sheet in electrolyte for electrophoretic deposition, wherein the deposition voltage is 145V, the deposition time is 1.5min, taking out the carbon fiber, ultrasonically cleaning the carbon fiber with deionized water for 8min, and drying the carbon fiber for 22h to obtain pretreated carbon fiber;
mixing and stirring the pretreated carbon fiber and absolute ethyl alcohol for 15min, ultrasonically dispersing for 35min, adding a silane coupling agent, ultrasonically dispersing for 25min, reacting for 5.5h in a water bath at 70 ℃, washing and drying to obtain modified carbon fiber; wherein the silane coupling agent is KH550;
(4) Placing silicon carbide powder into N-methyl pyrrolidone solution, placing in ice water bath, adding 2-bromo isobutyryl bromide under nitrogen environment, heating to 63 ℃, stirring for reaction for 19h, washing with absolute ethyl alcohol, and vacuum drying to obtain a material A;
taking a material A, cuprous bromide and glycidyl methacrylate, carrying out oscillation reaction for 1.1h in a closed environment, wherein the reaction temperature is 32 ℃, placing the material A, cuprous bromide and glycidyl methacrylate in a water bath at 63 ℃ after the reaction, standing for 22h, centrifugally filtering, washing and drying to obtain a material B;
taking a material B, cuprous bromide, methyl acrylate and pentamethyl diethylenetriamine, carrying out oscillation reaction for 1.3 hours in a closed environment, standing for 22 hours at the reaction temperature of 32 ℃, centrifugally filtering, washing, drying, and then soaking in a sodium hydroxide solution for 21 hours to obtain carboxylated silicon carbide;
(5) Dissolving polypropylene, modified carbon fiber and hydroxyapatite in deionized water, mixing and stirring for 15min, adding carboxylated silicon carbide, glass fiber and sodium carbonate solution, stirring and reacting for 25min, adding antioxidant, plasticizer, light stabilizer, lubricant and wear-resisting agent, uniformly mixing, drying, placing in a double-screw extruder, melting and mixing, and extruding to obtain the finished product.
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| CN117183518A (en) * | 2023-09-01 | 2023-12-08 | 青岛伟东包装有限公司 | High-ductility puncture-resistant plastic film and preparation method thereof |
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| Publication number | Publication date |
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| CN112679844B (en) | 2023-06-20 |
| CN112679844A (en) | 2021-04-20 |
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