CN114106446A - Cable insulation material - Google Patents
Cable insulation material Download PDFInfo
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- CN114106446A CN114106446A CN202111573650.1A CN202111573650A CN114106446A CN 114106446 A CN114106446 A CN 114106446A CN 202111573650 A CN202111573650 A CN 202111573650A CN 114106446 A CN114106446 A CN 114106446A
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- 239000012774 insulation material Substances 0.000 title claims abstract description 29
- 239000002639 bone cement Substances 0.000 claims abstract description 49
- 229920001903 high density polyethylene Polymers 0.000 claims abstract description 46
- 239000004700 high-density polyethylene Substances 0.000 claims abstract description 46
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 34
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 33
- 239000000853 adhesive Substances 0.000 claims abstract description 31
- 230000001070 adhesive effect Effects 0.000 claims abstract description 31
- 239000002994 raw material Substances 0.000 claims abstract description 25
- 239000004014 plasticizer Substances 0.000 claims abstract description 24
- 239000000314 lubricant Substances 0.000 claims abstract description 21
- 239000003365 glass fiber Substances 0.000 claims abstract description 19
- 239000000839 emulsion Substances 0.000 claims abstract description 17
- 229920002635 polyurethane Polymers 0.000 claims abstract description 17
- 239000004814 polyurethane Substances 0.000 claims abstract description 17
- 238000002360 preparation method Methods 0.000 claims abstract description 12
- 238000002156 mixing Methods 0.000 claims description 65
- 239000004734 Polyphenylene sulfide Substances 0.000 claims description 40
- 229920000069 polyphenylene sulfide Polymers 0.000 claims description 40
- 238000002844 melting Methods 0.000 claims description 25
- 230000008018 melting Effects 0.000 claims description 25
- 239000011347 resin Substances 0.000 claims description 23
- 229920005989 resin Polymers 0.000 claims description 23
- 239000004709 Chlorinated polyethylene Substances 0.000 claims description 22
- 239000006229 carbon black Substances 0.000 claims description 22
- 238000003756 stirring Methods 0.000 claims description 20
- 239000000835 fiber Substances 0.000 claims description 18
- 239000002105 nanoparticle Substances 0.000 claims description 16
- 229910000859 α-Fe Inorganic materials 0.000 claims description 16
- 229920002472 Starch Polymers 0.000 claims description 15
- 239000007864 aqueous solution Substances 0.000 claims description 15
- 238000001035 drying Methods 0.000 claims description 15
- 239000008107 starch Substances 0.000 claims description 15
- 235000019698 starch Nutrition 0.000 claims description 15
- 238000005303 weighing Methods 0.000 claims description 15
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 13
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 13
- 229920002430 Fibre-reinforced plastic Polymers 0.000 claims description 12
- 239000011151 fibre-reinforced plastic Substances 0.000 claims description 12
- 239000000243 solution Substances 0.000 claims description 11
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 10
- 239000004020 conductor Substances 0.000 claims description 6
- 239000000155 melt Substances 0.000 claims description 6
- 238000007334 copolymerization reaction Methods 0.000 claims description 5
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 238000012986 modification Methods 0.000 claims description 5
- 230000004048 modification Effects 0.000 claims description 5
- 235000013873 oxidized polyethylene wax Nutrition 0.000 claims description 5
- 239000000843 powder Substances 0.000 claims description 5
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 claims description 4
- 239000004209 oxidized polyethylene wax Substances 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims description 2
- 239000008116 calcium stearate Substances 0.000 claims description 2
- 235000013539 calcium stearate Nutrition 0.000 claims description 2
- 235000019359 magnesium stearate Nutrition 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 2
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims 1
- 238000005034 decoration Methods 0.000 claims 1
- 238000009413 insulation Methods 0.000 claims 1
- 239000001993 wax Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 6
- 239000011230 binding agent Substances 0.000 abstract description 4
- 238000005265 energy consumption Methods 0.000 abstract description 2
- 239000003381 stabilizer Substances 0.000 abstract description 2
- 230000000052 comparative effect Effects 0.000 description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- HHEAADYXPMHMCT-UHFFFAOYSA-N dpph Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1[N]N(C=1C=CC=CC=1)C1=CC=CC=C1 HHEAADYXPMHMCT-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000004299 exfoliation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012811 non-conductive material Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000000126 substance Substances 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
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/06—Polyethene
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/44—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins
- H01B3/441—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins from alkenes
-
- 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
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2265—Oxides; Hydroxides of metals of iron
- C08K2003/2272—Ferric oxide (Fe2O3)
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/02—Flame or fire retardant/resistant
-
- 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
- C08L2203/00—Applications
- C08L2203/20—Applications use in electrical or conductive gadgets
- C08L2203/202—Applications use in electrical or conductive gadgets use in electrical wires or wirecoating
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2207/00—Properties characterising the ingredient of the composition
- C08L2207/06—Properties of polyethylene
- C08L2207/062—HDPE
Abstract
The invention relates to the technical field of cable manufacturing, in particular to a cable insulation material which comprises the following raw materials in parts by mass: 50-60 parts by mass of high-density polyethylene (HDPE), 10-25 parts by mass of glass fiber, 6-9 parts by mass of modified antioxidant, 5-8 parts by mass of polyurethane emulsion, 1-5 parts by mass of modified bone glue binder, 2-5 parts by mass of plasticizer and 1-3 parts by mass of lubricant. The lubricant is used as a stabilizer, the glass fiber is dispersed on the surface of the cable, good insulativity can be obtained, the modified bone glue adhesive improves the bonding strength of raw materials, the plasticizer improves the surface tension of the cable, the preparation process is simple, the production stability is good, and the energy consumption is saved.
Description
Technical Field
The invention relates to the technical field of cable manufacturing, in particular to a cable insulating material.
Background
An insulated cable is a cable in which a layer of non-conductive material is uniformly and hermetically wrapped around the conductor, such as: resin, plastic, silicon rubber, PVC and the like to form an insulating layer, so that the insulated wire can be used for preventing accidents such as electric leakage, short circuit, electric shock and the like caused by the contact of the electric conductor and the outside.
The cable is oxidized after being used for a long time, and the cable is often scratched by a sharp object to influence the use of the product. Therefore, we propose a cable insulation material for solving the above problems.
Disclosure of Invention
The invention aims to solve the defects in the prior art and provides a cable insulating material.
A cable insulation material comprises the following raw materials in parts by mass:
50-60 parts by mass of high-density polyethylene (HDPE), 20-30 parts by mass of ferrite nanoparticles, 10-25 parts by mass of glass fibers, 6-9 parts by mass of modified antioxidant, 5-8 parts by mass of polyurethane emulsion, 1-5 parts by mass of modified bone glue adhesive, 2-5 parts by mass of plasticizer and 1-3 parts by mass of lubricant.
Preferably, the high-density polyethylene HDPE is added with phenolic FRP (fiber reinforced Plastic) and modified chlorinated polyethylene CPE (chlorinated polyethylene), wherein the content of the phenolic FRP is 28-30%, and the content of the modified chlorinated polyethylene CPE is 5-10%.
Preferably, the modified antioxidant is prepared by blending polyphenylene sulfide resin, carbon black and polyphenylene sulfide fibers as raw materials, wherein the mixing mass ratio of the polyphenylene sulfide resin, the carbon black and the polyphenylene sulfide fibers is 7:3: 5.
Preferably, the lubricant is a combination of one of methyl silicone oil, calcium stearate, magnesium stearate and zinc stearate and oxidized polyethylene wax according to a ratio of 1: 4.
Preferably, the oxidized polyethylene wax is one of oxidized polyethylene waxes with an acid value of 12-36 mgKOH/g and a weight-average molecular weight of 300-600 g/mol.
Preferably, the preparation method of the modified antioxidant comprises the following steps: weighing polyphenylene sulfide resin, carbon black and polyphenylene sulfide fiber according to a certain amount, putting the polyphenylene sulfide resin and the polyphenylene sulfide fiber into a mixing roll, and mixing and melting for 5-11 min at the temperature of 90-120 ℃; and (3) after uniformly stirring, adding the carbon black ground into powder, mixing and melting for 2-5 min, adding a proper amount of 2% ethanol water solution, continuously stirring for 15-20 min, and obtaining the modified antioxidant after stirring.
Preferably, the modified bone glue adhesive is prepared by graft copolymerization modification of a bone glue aqueous solution, starch and acrylic acid, wherein the mass ratio of the bone glue aqueous solution to the starch to the acrylic acid is 4:3:2, the starch and the bone glue aqueous solution are uniformly mixed, the acrylic acid is added according to the amount, the mixture is uniformly stirred after being mixed, and the modified bone glue adhesive is obtained after the stirring is finished.
A preparation method of a cable insulation material comprises the following steps:
s1, weighing the raw materials in proportion, putting the high-density polyethylene HDPE and the ferrite nanoparticles into an internal mixer, and mixing and melting for 5-10 min at the temperature of 90-120 ℃;
s2, adding a lubricant and glass fibers into the melt, mixing and melting for 3-6 min, adding a modified antioxidant, mixing and melting for 2-8 min;
s4, weighing the modified bone glue adhesive and the plasticizer, pouring the modified bone glue adhesive and the plasticizer into a mixing roll, and fully mixing for 5-10 min at the mixing temperature of 45-55 ℃;
and S5, adding polyurethane emulsion into the obtained melt according to the amount, uniformly mixing, then mixing for 20-30 min at the temperature of 120-135 ℃, extruding, granulating and drying the mixed product, and finally forming to obtain the cable insulation material, wherein the drying temperature is 60-85 ℃, and the drying time is 10-14 h.
Preferably, the twisting pitch ratio of the conductor is 12-15 times of the outer diameter of the conductor, the twisting directions of adjacent layers are opposite, and the innermost layer is in the right direction.
Compared with the prior art, the invention has the beneficial effects that:
1. in the invention, a proper amount of CPE is added into the high-density polyethylene HDPE, so that the melt viscosity can be reduced, the fluidity is improved, and the processing performance is improved; the coating also has good oil resistance, flame retardance and coloring performance;
2. in the invention, the modified antioxidant is prepared by taking the polyphenylene sulfide resin, the carbon black and the polyphenylene sulfide fiber as raw materials, the polyphenylene sulfide resin and the polyphenylene sulfide fiber have the advantages of excellent high temperature resistance, chemical resistance and flame retardancy, and the carbon black as a light shielding agent can play a good shielding effect on ultraviolet rays;
3. in the invention, the lubricant is used as a stabilizer, the glass fiber is dispersed on the surface of the cable, good insulativity can be obtained, the modified bone glue adhesive improves the bonding strength of raw materials, the plasticizer improves the surface tension of the cable, the preparation process is simple, the production stability is good, and the energy consumption is saved.
Detailed Description
The present invention will be further illustrated with reference to the following specific examples.
Example 1:
a cable insulation material comprises the following raw materials in parts by mass:
50 parts by mass of high-density polyethylene (HDPE), 20 parts by mass of ferrite nanoparticles, 10 parts by mass of glass fibers, 6 parts by mass of modified antioxidant, 5 parts by mass of polyurethane emulsion, 1 part by mass of modified bone glue adhesive, 2 parts by mass of plasticizer and 1 part by mass of lubricant.
Example 2:
a cable insulation material comprises the following raw materials in parts by mass:
55 parts by mass of high-density polyethylene (HDPE), 25 parts by mass of ferrite nanoparticles, 15 parts by mass of glass fibers, 7 parts by mass of modified antioxidant, 8 parts by mass of polyurethane emulsion, 3 parts by mass of modified bone glue adhesive, 3 parts by mass of plasticizer and 2 parts by mass of lubricant.
Example 3:
a cable insulation material comprises the following raw materials in parts by mass:
60 parts by mass of high-density polyethylene (HDPE), 30 parts by mass of ferrite nanoparticles, 25 parts by mass of glass fibers, 9 parts by mass of modified antioxidant, 8 parts by mass of polyurethane emulsion, 5 parts by mass of modified bone glue adhesive, 5 parts by mass of plasticizer and 3 parts by mass of lubricant.
In the above embodiments 1 to 3, the high density polyethylene HDPE is added with the phenolic FRP and the modified chlorinated polyethylene CPE, wherein the phenolic FRP content is 28 to 30%, and the modified chlorinated polyethylene CPE content is 5 to 10%;
the modified antioxidant is prepared by blending raw materials of polyphenylene sulfide resin, carbon black and polyphenylene sulfide fiber, wherein the mixing mass ratio of the polyphenylene sulfide resin, the carbon black and the polyphenylene sulfide fiber is 7:3: 5; the preparation method comprises the following steps: the preparation method of the modified antioxidant comprises the following steps: weighing polyphenylene sulfide resin, carbon black and polyphenylene sulfide fiber according to a certain amount, putting the polyphenylene sulfide resin and the polyphenylene sulfide fiber into a mixing roll, and mixing and melting for 5-11 min at the temperature of 90-120 ℃; after uniformly stirring, adding the carbon black ground into powder, mixing and melting for 2-5 min, adding a proper amount of 2% ethanol water solution, continuously stirring for 15-20 min, and obtaining a modified antioxidant after stirring;
the modified bone glue adhesive is prepared by graft copolymerization modification of a bone glue aqueous solution, starch and acrylic acid, wherein the mass ratio of the bone glue aqueous solution to the starch to the acrylic acid is 4:3:2, the starch and the bone glue aqueous solution are uniformly mixed, the acrylic acid is added according to the amount, the mixture is uniformly stirred after being mixed, and the modified bone glue adhesive is obtained after the stirring is finished.
In each of examples 1 to 3, the insulated cable was prepared by the following steps:
s1, weighing the raw materials in proportion, putting the high-density polyethylene HDPE and the ferrite nanoparticles into an internal mixer, and mixing and melting for 5-10 min at the temperature of 90-120 ℃;
s2, adding a lubricant and glass fibers into the melt, mixing and melting for 3-6 min, adding a modified antioxidant, mixing and melting for 2-8 min;
s4, weighing the modified bone glue adhesive and the plasticizer, pouring the modified bone glue adhesive and the plasticizer into a mixing roll, and fully mixing for 5-10 min at the mixing temperature of 45-55 ℃;
and S5, adding polyurethane emulsion into the obtained melt according to the amount, uniformly mixing, then mixing for 20-30 min at the temperature of 120-135 ℃, extruding, granulating and drying the mixed product, and finally forming to obtain the cable insulation material, wherein the drying temperature is 60-85 ℃, and the drying time is 10-14 h.
Test one: determination of the Oxidation resistance of insulated Cable
Comparative example 1:
a cable insulation material comprises the following raw materials in parts by mass:
50 parts by mass of high-density polyethylene (HDPE), 20 parts by mass of ferrite nanoparticles, 10 parts by mass of glass fibers, 6 parts by mass of antioxidants, 5 parts by mass of polyurethane emulsion, 1 part by mass of modified bone glue binder, 2 parts by mass of plasticizer and 1 part by mass of lubricant.
Comparative example 2:
a cable insulation material comprises the following raw materials in parts by mass:
55 parts by mass of high-density polyethylene (HDPE), 25 parts by mass of ferrite nanoparticles, 15 parts by mass of glass fibers, 7 parts by mass of antioxidant, 8 parts by mass of polyurethane emulsion, 3 parts by mass of modified bone glue adhesive, 3 parts by mass of plasticizer and 2 parts by mass of lubricant.
Comparative example 3:
a cable insulation material comprises the following raw materials in parts by mass:
60 parts by mass of high-density polyethylene (HDPE), 30 parts by mass of ferrite nanoparticles, 25 parts by mass of glass fibers, 9 parts by mass of antioxidant, 8 parts by mass of polyurethane emulsion, 5 parts by mass of modified bone glue adhesive, 5 parts by mass of plasticizer and 3 parts by mass of lubricant.
In the comparative examples 1-3, the high-density polyethylene HDPE is added with the phenolic FRP and the modified chlorinated polyethylene CPE, wherein the content of the phenolic FRP is 28-30%, and the content of the modified chlorinated polyethylene CPE is 5-10%;
the antioxidant is prepared by mixing polyphenylene sulfide resin and carbon black serving as raw materials, wherein the mixing mass ratio of the polyphenylene sulfide resin to the carbon black is 7: 3; the preparation method comprises the following steps: the preparation method of the antioxidant comprises the following steps: weighing polyphenylene sulfide resin and carbon black according to a certain amount, putting the polyphenylene sulfide resin into a mixing roll, and mixing and melting for 5-11 min at the temperature of 90-120 ℃; after uniformly stirring, adding the carbon black ground into powder, mixing and melting for 2-5 min, adding a proper amount of 2% ethanol water solution, continuously stirring for 15-20 min, and obtaining an antioxidant after stirring;
the modified bone glue adhesive is prepared by graft copolymerization modification of a bone glue aqueous solution, starch and acrylic acid, wherein the mass ratio of the bone glue aqueous solution to the starch to the acrylic acid is 4:3:2, the starch and the bone glue aqueous solution are uniformly mixed, the acrylic acid is added according to the amount, the mixture is uniformly stirred after being mixed, and the modified bone glue adhesive is obtained after the stirring is finished.
In each of comparative examples 1 to 3, the insulated cable was prepared by the following steps:
s1, weighing the raw materials in proportion, putting the high-density polyethylene HDPE and the ferrite nanoparticles into an internal mixer, and mixing and melting for 5-10 min at the temperature of 90-120 ℃;
s2, adding a lubricant and glass fibers into the melt, mixing and melting for 3-6 min, adding a modified antioxidant, mixing and melting for 2-8 min;
s4, weighing the modified bone glue adhesive and the plasticizer, pouring the modified bone glue adhesive and the plasticizer into a mixing roll, and fully mixing for 5-10 min at the mixing temperature of 45-55 ℃;
and S5, adding polyurethane emulsion into the obtained melt according to the amount, uniformly mixing, then mixing for 20-30 min at the temperature of 120-135 ℃, extruding, granulating and drying the mixed product, and finally forming to obtain the cable insulation material, wherein the drying temperature is 60-85 ℃, and the drying time is 10-14 h.
The following tests were carried out on the cables of examples 1 to 3 and comparative examples 1 to 3, respectively:
dropwise adding 3mL of DPPH methanol solution (the mass fraction of the DPPH methanol solution is 0.004%) on the surface of the cable, leveling the solution evenly, standing the solution for 30 minutes, measuring the absorbance at a wavelength of 517nm, calculating the inhibition rate of the solution, and recording the inhibition rate in the following table:
as can be seen from the above data, the oxidation resistance of the cables of examples, comparative examples and reference examples is the most susceptible to oxidation of the cable surface layer prepared in the examples, reference examples and comparative examples, i.e., comparative examples, in order from strong to weak, and thus it can be seen that the addition of the antioxidant has an effect of improving the oxidation resistance of the cable surface layer.
And (2) test II: determination of the resistance to cracking of an insulated Cable
Comparative example 4:
a cable insulation material comprises the following raw materials in parts by mass:
50 parts by mass of high-density polyethylene (HDPE), 20 parts by mass of ferrite nanoparticles, 10 parts by mass of glass fibers, 6 parts by mass of modified antioxidant, 5 parts by mass of polyurethane emulsion, 1 part by mass of bone glue adhesive, 2 parts by mass of plasticizer and 1 part by mass of lubricant.
Comparative example 5:
a cable insulation material comprises the following raw materials in parts by mass:
55 parts by mass of high-density polyethylene (HDPE), 25 parts by mass of ferrite nanoparticles, 15 parts by mass of glass fibers, 7 parts by mass of modified antioxidant, 8 parts by mass of polyurethane emulsion, 3 parts by mass of bone glue binder, 3 parts by mass of plasticizer and 2 parts by mass of lubricant.
Comparative example 6:
a cable insulation material comprises the following raw materials in parts by mass:
60 parts by mass of high-density polyethylene (HDPE), 30 parts by mass of ferrite nanoparticles, 25 parts by mass of glass fibers, 9 parts by mass of modified antioxidant, 8 parts by mass of polyurethane emulsion, 5 parts by mass of bone glue binder, 5 parts by mass of plasticizer and 3 parts by mass of lubricant.
In the comparative examples 4-6, the high-density polyethylene HDPE is added with the phenolic FRP and the modified chlorinated polyethylene CPE, wherein the content of the phenolic FRP is 28-30%, and the content of the modified chlorinated polyethylene CPE is 5-10%;
the modified antioxidant is prepared by blending raw materials of polyphenylene sulfide resin, carbon black and polyphenylene sulfide fiber, wherein the mixing mass ratio of the polyphenylene sulfide resin, the carbon black and the polyphenylene sulfide fiber is 7:3: 5; the preparation method comprises the following steps: the preparation method of the modified antioxidant comprises the following steps: weighing polyphenylene sulfide resin, carbon black and polyphenylene sulfide fiber according to a certain amount, putting the polyphenylene sulfide resin and the polyphenylene sulfide fiber into a mixing roll, and mixing and melting for 5-11 min at the temperature of 90-120 ℃; after uniformly stirring, adding the carbon black ground into powder, mixing and melting for 2-5 min, adding a proper amount of 2% ethanol water solution, continuously stirring for 15-20 min, and obtaining a modified antioxidant after stirring;
the bone glue adhesive is prepared by graft copolymerization modification of a bone glue aqueous solution and starch, wherein the mass ratio of the bone glue aqueous solution to the starch is 4:3, the starch and the bone glue aqueous solution are uniformly mixed, the mixture is uniformly stirred, and the bone glue adhesive is obtained after the stirring is finished.
In comparative examples 4 to 6, the insulated cables were prepared by the following steps:
s1, weighing the raw materials in proportion, putting the high-density polyethylene HDPE and the ferrite nanoparticles into an internal mixer, and mixing and melting for 5-10 min at the temperature of 90-120 ℃;
s2, adding a lubricant and glass fibers into the melt, mixing and melting for 3-6 min, adding a modified antioxidant, mixing and melting for 2-8 min;
s4, weighing the modified bone glue adhesive and the plasticizer, pouring the modified bone glue adhesive and the plasticizer into a mixing roll, and fully mixing for 5-10 min at the mixing temperature of 45-55 ℃;
and S5, adding polyurethane emulsion into the obtained melt according to the amount, uniformly mixing, then mixing for 20-30 min at the temperature of 120-135 ℃, extruding, granulating and drying the mixed product, and finally forming to obtain the cable insulation material, wherein the drying temperature is 60-85 ℃, and the drying time is 10-14 h.
The following tests were carried out on the cables of examples 1 to 3 and comparative examples 4 to 6, respectively:
drawing two crossed straight lines (each 40 mm) on the surface of the coating film, wherein the crossing angle is 30-45 degrees, and the coating film is cut through to the ground material;
and secondly, adhering a cutting position by using a pressure sensitive adhesive tape, and inspecting the film falling condition of the cross cutting area after tearing so as to judge the adhesive force strength.
The method for rating the falling-off condition of the coating film is shown in the following table:
grading | Description of the invention |
5A | Without peeling off |
4A | There is a mark of peeling at the position of the cross |
3A | At the position of 1.6mm crossing to the other side, a serrated peeling notch is arranged |
2A | At a position 3.2mm across to the other side,with serrated peel-off cuts |
1A | Large area exfoliation in the cross-hatched area |
0A | All peeling off in the cross-cut region |
The tests were carried out on days 1 to 3 after the cable was produced, and the test results are shown in the following table:
from the above test results, in examples 1 to 3, the film layer formation speed of the cable was fast within 1 to 3 days after the production, so that the cable was not easily cracked, while in comparative examples 4 to 6, the film layer formation speed of the cable was slow within 1 to 3 days after the production, so that the cable was easily scratched, so that the cable was peeled off from the surface of the sheath. Therefore, the addition of the acrylic acid can further improve the anti-damage performance of the glass cable.
The above description is only for the preferred embodiment of the present invention, but the scope of the present invention is not limited thereto, and any person skilled in the art should be considered to be within the technical scope of the present invention, and the technical solutions and the inventive concepts thereof according to the present invention should be equivalent or changed within the scope of the present invention.
Claims (10)
1. The cable insulation material is characterized by comprising the following raw materials in parts by mass:
50-60 parts by mass of high-density polyethylene (HDPE), 20-30 parts by mass of ferrite nanoparticles, 10-25 parts by mass of glass fibers, 6-9 parts by mass of modified antioxidant, 5-8 parts by mass of polyurethane emulsion, 1-5 parts by mass of modified bone glue adhesive, 2-5 parts by mass of plasticizer and 1-3 parts by mass of lubricant.
2. The cable insulation material as claimed in claim 1, wherein the high density polyethylene HDPE is added with phenolic FRP (fiber reinforced Plastic) and modified chlorinated polyethylene CPE, wherein the phenolic FRP content is 28-30%, and the modified chlorinated polyethylene CPE content is 5-10%.
3. The cable insulation material as claimed in claim 1, wherein the modified antioxidant is prepared by blending polyphenylene sulfide resin, carbon black and polyphenylene sulfide fiber as raw materials, and the mixing mass ratio of the polyphenylene sulfide resin, the carbon black and the polyphenylene sulfide fiber is 7:3: 5.
4. The cable insulation material as claimed in claim 1, wherein the lubricant is a combination of one of methyl silicone oil, calcium stearate, magnesium stearate, zinc stearate and polyethylene oxide wax in a ratio of 1: 4.
5. The cable insulation material according to claim 4, wherein the oxidized polyethylene wax is one of oxidized polyethylene waxes having an acid value of 12 to 36mgKOH/g and a weight average molecular weight of 300 to 600 g/mol.
6. The cable insulation material as claimed in claim 3, wherein the modified antioxidant is prepared by the following steps: weighing polyphenylene sulfide resin, carbon black and polyphenylene sulfide fiber according to a certain amount, putting the polyphenylene sulfide resin and the polyphenylene sulfide fiber into a mixing roll, and mixing and melting for 5-11 min at the temperature of 90-120 ℃; and (3) after uniformly stirring, adding the carbon black ground into powder, mixing and melting for 2-5 min, adding a proper amount of 2% ethanol water solution, continuously stirring for 15-20 min, and obtaining the modified antioxidant after stirring.
7. The cable insulation material of claim 1, wherein the modified bone glue adhesive is prepared by graft copolymerization modification of a bone glue aqueous solution, starch and acrylic acid, wherein the mass ratio of the bone glue aqueous solution to the starch to the acrylic acid is 4:3:2, the starch and the bone glue aqueous solution are uniformly mixed, the acrylic acid is added according to the amount, the mixture is uniformly stirred, and the modified bone glue adhesive is obtained after the stirring is finished.
8. The preparation method of the cable insulation material is characterized by comprising the following steps:
s1, weighing the raw materials in proportion, putting the high-density polyethylene HDPE and the ferrite nanoparticles into an internal mixer, and mixing and melting for 5-10 min at the temperature of 90-120 ℃;
s2, adding a lubricant and glass fibers into the melt, mixing and melting for 3-6 min, adding a modified antioxidant, mixing and melting for 2-8 min;
s4, weighing the modified bone glue adhesive and the plasticizer, pouring the modified bone glue adhesive and the plasticizer into a mixing roll, and fully mixing for 5-10 min at the mixing temperature of 45-55 ℃;
and S5, adding polyurethane emulsion into the obtained melt according to the amount, uniformly mixing, then mixing for 20-30 min at the temperature of 120-135 ℃, extruding, granulating and drying the mixed product, and finally forming to obtain the cable insulation material, wherein the drying temperature is 60-85 ℃, and the drying time is 10-14 h.
9. The method for preparing a cable insulation material as claimed in claim 8, wherein the conductor has a twist pitch ratio of 12 to 15 times the outer diameter of the conductor, adjacent layers have opposite twist directions, and the innermost layer is in a right direction.
10. Use of a cable insulation according to claims 1-7 for the preparation of low voltage cables, medium voltage cables, high voltage cables, automotive cables, communication cables and home decoration cables.
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Publication number | Priority date | Publication date | Assignee | Title |
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CN101440269A (en) * | 2007-11-22 | 2009-05-27 | 国家淀粉及化学投资控股公司 | Adhesive, preparation and use thereof |
CN106750741A (en) * | 2016-11-28 | 2017-05-31 | 安徽瑞研新材料技术研究院有限公司 | A kind of refractory polyethylene material cable |
CN111363226A (en) * | 2020-04-09 | 2020-07-03 | 江苏法斯特电力科技有限公司 | Low-temperature-resistant high-density polyethylene power cable protection pipe |
CN112646262A (en) * | 2020-12-21 | 2021-04-13 | 河北中联银杉新材料有限公司 | Insulating material of photovoltaic cable |
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2021
- 2021-12-21 CN CN202111573650.1A patent/CN114106446A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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CN101440269A (en) * | 2007-11-22 | 2009-05-27 | 国家淀粉及化学投资控股公司 | Adhesive, preparation and use thereof |
CN106750741A (en) * | 2016-11-28 | 2017-05-31 | 安徽瑞研新材料技术研究院有限公司 | A kind of refractory polyethylene material cable |
CN111363226A (en) * | 2020-04-09 | 2020-07-03 | 江苏法斯特电力科技有限公司 | Low-temperature-resistant high-density polyethylene power cable protection pipe |
CN112646262A (en) * | 2020-12-21 | 2021-04-13 | 河北中联银杉新材料有限公司 | Insulating material of photovoltaic cable |
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