CN108641203A - Antiultraviolet stable type cable jacket material and preparation method thereof is worn in a kind of resistance - Google Patents

Antiultraviolet stable type cable jacket material and preparation method thereof is worn in a kind of resistance Download PDF

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Publication number
CN108641203A
CN108641203A CN201810300087.2A CN201810300087A CN108641203A CN 108641203 A CN108641203 A CN 108641203A CN 201810300087 A CN201810300087 A CN 201810300087A CN 108641203 A CN108641203 A CN 108641203A
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parts
mixing
antiultraviolet
cable jacket
worn
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叶明玉
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ANHUI GUOHUA CABLE GROUP Co Ltd
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ANHUI GUOHUA CABLE GROUP Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/50Amines
    • C08G59/5033Amines aromatic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/26Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/30Insulators 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
    • H01B3/44Insulators 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
    • H01B3/441Insulators 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
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/24Acids; Salts thereof
    • C08K3/26Carbonates; Bicarbonates
    • C08K2003/265Calcium, strontium or barium carbonate
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/32Phosphorus-containing compounds
    • C08K2003/321Phosphates
    • C08K2003/322Ammonium phosphate
    • C08K2003/323Ammonium polyphosphate
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/011Nanostructured additives
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/26Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
    • C08L2023/40Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment by reaction with compounds changing molecular weight
    • C08L2023/44Coupling; Molecular weight increase
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/08Stabilised against heat, light or radiation or oxydation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00Applications
    • C08L2203/20Applications use in electrical or conductive gadgets
    • C08L2203/202Applications use in electrical or conductive gadgets use in electrical wires or wirecoating
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • C08L2205/035Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend

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  • Spectroscopy & Molecular Physics (AREA)
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Abstract

The invention discloses a kind of resistances to wear antiultraviolet stable type cable jacket material, is made of the raw material below according to parts by weight:10 40 parts of bentonite, 5 25 parts of white carbon, 4 16 parts of crosslinked polyethylene, 5 15 parts of glass fibre, 3 13 parts of polyvinyl chloride resin, 5 25 parts of nano-calcium carbonate, 2 14 parts of modified epoxy, 4 16 parts of acetone sodium, 7 21 parts of calcium stearate, 2 14 parts of ammonium polyphosphate, 3 13 parts of diethyl amino propylamine, 4 18 parts of diaminodiphenyl-methane, 3 13 parts of polyvinyl formal, 4 16 parts of 24 dihydroxy benaophenonel.The present invention has many advantages, such as that stretch-proof, antiultraviolet and structural strength are high.

Description

Antiultraviolet stable type cable jacket material and preparation method thereof is worn in a kind of resistance
Technical field
The present invention relates to a kind of protective cover materials more particularly to a kind of resistance to wear antiultraviolet stable type cable jacket material and its system Preparation Method.
Background technology
Currently, cable is typically by several or several groups of conducting wires(Every group at least two)The electricity for the similar rope being twisted Cable, mutually insulated between every group of conducting wire, and be often twisted into around a center, entire outside is surrounded by the coating of high-insulation, There is cable interior energization, the feature of external insulation, cable to have power cable, control cable, compensating cable, shielded cable, high-temperature electric Cable, computer cable, signal cable, coaxial cable, fire-resisting cable, cable for ship, mine cable, aluminium alloy cable etc., it Be all made of sub-thread or stranded conductor and insulating layer, for connecting circuit, electric appliance etc., the manufacture of electric wire with it is most of The mode of production of electronic product is entirely different, and another part is assembled into component by electronic product generally use, multiple components refill It is made into separate unit product, product is measured with number of units or number of packages, and electric wire is with length for basic measurement unit, all electric wires All it is to add insulation, shielding, stranding, sheath etc. since being processed conductor layer by layer in the periphery of conductor and electric wire is made Cable product, product structure is more complicated, and the level of superposition is more.
But current cable used on the market was used because the material added in the production process is unreasonable in cable The case where being in direct sunlight in journey for a long time, can lead to the aging of cable itself, the case where fracture, so as to cause in cable Portion ruptures, and the case where causing short circuit or leak electricity, and since the material that cable cover(ing) uses is unreasonable, leads to cable seal performance not It is good, in rupture, steam is invaded, causes dielectric strength to reduce, occurs breakdown situation so as to cause cable, be unfavorable for people Long-time service.
Invention content
In order to overcome the defect of the above-mentioned prior art, the object of the present invention is to provide a kind of resistances to wear antiultraviolet stable type Cable jacket material and preparation method thereof.
The present invention takes following technical scheme to realize:Antiultraviolet stable type cable jacket material is worn in a kind of resistance, It is characterized in that, being made of the raw material below according to parts by weight:10-40 parts of bentonite, 5-25 parts of white carbon, crosslinked polyethylene 4-16 parts, 5-15 parts of glass fibre, 3-13 parts of polyvinyl chloride resin, 5-25 parts of nano-calcium carbonate, 2-14 parts of modified epoxy, acetone 4-16 parts of sodium, 7-21 parts of calcium stearate, 2-14 parts of ammonium polyphosphate, 3-13 parts of diethyl amino propylamine, diaminodiphenyl-methane 4-18 parts, 3-13 parts of polyvinyl formal, 4-16 parts of 2-4 dihydroxy benaophenonels.
The preparation method of the modified epoxy is as follows:
Epoxy resin is heated in a kettle, heating time 60-120min, poly- second is added after the completion of heating Alkene, dibasic lead stearate, phosphorus curing agent and diethylenetriamine, are stirred again, and mixing time 80min is stirred It is passed through nitrogen after the completion of mixing, silane coupling agent is added in a nitrogen environment, fully carries out stewing process after reaction, obtains modified ring Oxygen resin.
Antiultraviolet stable type cable jacket material is worn in a kind of above-mentioned resistance, by below according to the raw material group of parts by weight At:10-35 parts of bentonite, 5-20 parts of white carbon, 4-14 parts of crosslinked polyethylene, 5-13 parts of glass fibre, 3-11 parts of polyvinyl chloride resin, 5-22 parts of nano-calcium carbonate, 2-12 parts of modified epoxy, 4 parts of acetone sodium 4-1,7-19 parts of calcium stearate, ammonium polyphosphate 2- 12 parts, 3-11 parts of diethyl amino propylamine, 4-16 parts of diaminodiphenyl-methane, 3-11 parts of polyvinyl formal, 2-4 dihydroxy 4-14 parts of benzophenone.
Antiultraviolet stable type cable jacket material is worn in a kind of above-mentioned resistance, by below according to the raw material group of parts by weight At:25 parts of bentonite, 15 parts of white carbon, 10 parts of crosslinked polyethylene, 10 parts of glass fibre, 8 parts of polyvinyl chloride resin, nano-calcium carbonate 15 Part, 8 parts of modified epoxy, 10 parts of acetone sodium, 14 parts of calcium stearate, 8 parts of ammonium polyphosphate, 8 parts of diethyl amino propylamine, diamino 11 parts of base diphenyl methane, 8 parts of polyvinyl formal, 10 parts of 2-4 dihydroxy benaophenonels.
The preparation method of antiultraviolet stable type cable jacket material is worn in a kind of above-mentioned resistance, is comprised the steps of:
(1)The parts by weight for weighing each material in claim 3, by bentonite, white carbon, crosslinked polyethylene, glass fibre, Polyvinyl chloride resin, nano-calcium carbonate, acetone sodium, calcium stearate, ammonium polyphosphate, diethyl amino propylamine, diaminodiphenyl-methane, Polyvinyl formal, 2-4 dihydroxy benaophenonels, which are put into mixer, carries out mixing mixing, and smelting temperature is 70-85 DEG C, close The refining time is 30min;
(2)Modified epoxy will be added in the material obtained in step 1, adjust mixer temperature, mixer temperature is 80-95 DEG C, mixing mixing time is 20min, obtains blend glue stuff;
(3)The material obtained in step 2 is subjected to vulcanizing treatment, curing temperature is 150-170 DEG C, vulcanization time 15min;
(4)The material that step 3 is obtained carries out mill processing with open mill, and mixing temperature is 50-65 DEG C;
(5)It by the materials result obtained in step 4, opens item and is cooled to room temperature, obtain finished product.
Antiultraviolet stable type cable jacket material is worn in a kind of above-mentioned resistance, and 11 parts of the diaminodiphenyl-methane gathers 8 parts of vinyl formal, 2-4 dihydroxy benaophenonel materials weight part ratio be 1:2:1.
In summary the invention has the advantages that:The present invention has stretch-proof, antiultraviolet and structural strength The advantages that high, can adjust the molecular distribution of epoxy resin, while the modified ring by modified epoxy made from modification Oxygen resin and diethyl amino propylamine phase reaction, included in the functional group and diethyl amino propylamine in the modified epoxy Two active hydrogens and tertiary amino are reacted, and activation energy of curing reaction is reduced, and make material that irreversible variation occur, to The effective heat resistance and corrosion resistance for improving cable jacket material;The diaminodiphenyl-methane can be used as modified ring The curing agent of oxygen resin avoids cable jacket material from using so as to further increase the structural strength of cable jacket material The case where being broken in journey;Its structure of the polyvinyl formal is six-membered ring structure, because its structural property determines to change Material has the acid-proof alkaline of higher toughness and stabilization, and the polyvinyl formal is in the work of modified epoxy A small amount of intermolecular cross-linking can be formed under, this intermolecular cross-linking can effectively inhibit the formation of high-crystallinity, and make electricity The inner molecular structure of cable protective cover material is more uniformly distributed, to keep cable jacket material more stable in preparation process;The 2-4 bis- Tertiary amino in dihydroxy benaophenonel and modified epoxy reacts to form long chain alkane group, and it is water-soluble can effectively to improve its Property, to synthesize Water-soluble UV-absorbents, preferable absorption ultraviolet light can be had by being added in cable jacket material Advantage avoids electricity so as to prevent cable from making ultraviolet light to the injury caused by cable cover(ing) in air because being exposed to for a long time A problem that cable sheath is cracking effectively extends the service life of cable, convenient for people to use.
Specific implementation mode
The preparation method of the modified epoxy is as follows:
Epoxy resin is heated in a kettle, heating time 60-120min, poly- second is added after the completion of heating Alkene, dibasic lead stearate, phosphorus curing agent and diethylenetriamine, are stirred again, and mixing time 80min is stirred It is passed through nitrogen after the completion of mixing, silane coupling agent is added in a nitrogen environment, fully carries out stewing process after reaction, obtains modified ring Oxygen resin.
Embodiment 1
Weigh 10 parts of bentonite, 5 parts of white carbon, 4 parts of crosslinked polyethylene, 5 parts of glass fibre, 3 parts of polyvinyl chloride resin, nano-calcium carbonate 5 Part, 2 parts of modified epoxy, 4 parts of acetone sodium, 7 parts of calcium stearate, 2 parts of ammonium polyphosphate, 3 parts of diethyl amino propylamine, diamino 4 parts of diphenyl methane, 3 parts of polyvinyl formal, 4 parts of 2-4 dihydroxy benaophenonels,(1)Weigh each material in embodiment 1 Parts by weight, by bentonite, white carbon, crosslinked polyethylene, glass fibre, polyvinyl chloride resin, nano-calcium carbonate, acetone sodium, stearic acid Calcium, ammonium polyphosphate, diethyl amino propylamine, diaminodiphenyl-methane, polyvinyl formal, 2-4 dihydroxy benaophenonels It is put into mixer and carries out mixing mixing, smelting temperature is 70-85 DEG C, mixing time 30min;(2)By what is obtained in step 1 Modified epoxy is added in material, adjusts mixer temperature, mixer temperature is 80-95 DEG C, and mixing mixing time is 20min obtains blend glue stuff;(3)The material obtained in step 2 is subjected to vulcanizing treatment, curing temperature is 150-170 DEG C, sulphur The change time is 15min;(4)The material that step 3 is obtained carries out mill processing with open mill, and mixing temperature is 50-65 DEG C;(5) It by the materials result obtained in step 4, opens item and is cooled to room temperature, obtain finished product.
Embodiment 2
Weigh 25 parts of bentonite, 15 parts of white carbon, 10 parts of crosslinked polyethylene, 10 parts of glass fibre, 8 parts of polyvinyl chloride resin, nano-calcium carbonate 15 parts of calcium, 8 parts of modified epoxy, 10 parts of acetone sodium, 14 parts of calcium stearate, 8 parts of ammonium polyphosphate, 8 parts of diethyl amino propylamine, 11 parts of diaminodiphenyl-methane, 8 parts of polyvinyl formal, 10 parts of 2-4 dihydroxy benaophenonels,(1)It weighs in embodiment 2 The parts by weight of each material, by bentonite, white carbon, crosslinked polyethylene, glass fibre, polyvinyl chloride resin, nano-calcium carbonate, acetone Sodium, calcium stearate, ammonium polyphosphate, diethyl amino propylamine, diaminodiphenyl-methane, polyvinyl formal, 2-4 dihydroxy Benzophenone, which is put into mixer, carries out mixing mixing, and smelting temperature is 70-85 DEG C, mixing time 30min;(2)By step 1 In modified epoxy is added in obtained material, adjust mixer temperature, mixer temperature is 80-95 DEG C, when mixing mixing Between be 20min, obtain blend glue stuff;(3)The material obtained in step 2 is subjected to vulcanizing treatment, curing temperature 150-170 DEG C, vulcanization time 15min;(4)The material that step 3 is obtained carries out mill processing, mixing temperature 50-65 with open mill ℃;(5)It by the materials result obtained in step 4, opens item and is cooled to room temperature, obtain finished product.
Embodiment 3
Weigh 40 parts of bentonite, 25 parts of white carbon, 16 parts of crosslinked polyethylene, 15 parts of glass fibre, 13 parts of polyvinyl chloride resin, nano-sized carbon 25 parts of sour calcium, 14 parts of modified epoxy, 16 parts of acetone sodium, 21 parts of calcium stearate, 14 parts of ammonium polyphosphate, diethyl amino propylamine 13 parts, 18 parts of diaminodiphenyl-methane, 13 parts of polyvinyl formal, 16 parts of 2-4 dihydroxy benaophenonels,(1)Weigh reality The parts by weight for applying each material in example 3, by bentonite, white carbon, crosslinked polyethylene, glass fibre, polyvinyl chloride resin, nano-calcium carbonate Calcium, acetone sodium, calcium stearate, ammonium polyphosphate, diethyl amino propylamine, diaminodiphenyl-methane, polyvinyl formal, 2- 4 dihydroxy benaophenonels, which are put into mixer, carries out mixing mixing, and smelting temperature is 70-85 DEG C, mixing time 30min;(2) Modified epoxy will be added in the material obtained in step 1, adjust mixer temperature, mixer temperature is 80-95 DEG C, mixing Mixing time is 20min, obtains blend glue stuff;(3)The material obtained in step 2 is subjected to vulcanizing treatment, curing temperature is 150-170 DEG C, vulcanization time 15min;(4)The material that step 3 is obtained carries out mill processing with open mill, and mixing temperature is 50-65℃;(5)It by the materials result obtained in step 4, opens item and is cooled to room temperature, obtain finished product.
Comparative example 1
Weigh 10 parts of bentonite, 5 parts of white carbon, 4 parts of crosslinked polyethylene, 5 parts of glass fibre, 3 parts of polyvinyl chloride resin, nano-calcium carbonate 5 Part, 4 parts of acetone sodium, 7 parts of calcium stearate, 2 parts of ammonium polyphosphate, 3 parts of diethyl amino propylamine, 3 parts of polyvinyl formal, 2-4 4 parts of dihydroxy benaophenonel,(1)The parts by weight for weighing each material in comparative example 1, by bentonite, white carbon, the poly- second of crosslinking Alkene, glass fibre, polyvinyl chloride resin, nano-calcium carbonate, acetone sodium, calcium stearate, ammonium polyphosphate, diethyl amino propylamine, polyethylene Alcohol formal, 2-4 dihydroxy benaophenonels, which are put into mixer, carries out mixing mixing, and smelting temperature is 70-85 DEG C, mixing time For 30min;(2)The material obtained in step 2 is subjected to vulcanizing treatment, curing temperature is 150-170 DEG C, and vulcanization time is 15min;(3)The material that step 3 is obtained carries out mill processing with open mill, and mixing temperature is 50-65 DEG C;(4)It will be in step 4 Obtained materials result is opened item and is cooled to room temperature, and finished product is obtained.
Comparative example 2
Weigh 25 parts of bentonite, 15 parts of white carbon, 10 parts of crosslinked polyethylene, 10 parts of glass fibre, 8 parts of polyvinyl chloride resin, nano-calcium carbonate 15 parts of calcium, 10 parts of acetone sodium, 14 parts of calcium stearate, 8 parts of ammonium polyphosphate, 8 parts of diethyl amino propylamine, diaminodiphenyl-methane 11 parts,(1)The parts by weight for weighing each material in embodiment 2, by bentonite, white carbon, crosslinked polyethylene, glass fibre, PVC Resin, nano-calcium carbonate, acetone sodium, calcium stearate, ammonium polyphosphate, diethyl amino propylamine, diaminodiphenyl-methane are put into Mixing mixing is carried out in mixer, smelting temperature is 70-85 DEG C, mixing time 30min;(2)The material that will be obtained in step 2 Vulcanizing treatment is carried out, curing temperature is 150-170 DEG C, vulcanization time 15min;(3)The material open mill that step 3 is obtained Mill processing is carried out, mixing temperature is 50-65 DEG C;(4)It by the materials result obtained in step 4, opens item and is cooled to room temperature, obtain Finished product.
Comparative example 3
Weigh 40 parts of bentonite, 25 parts of white carbon, 16 parts of crosslinked polyethylene, 15 parts of glass fibre, 13 parts of polyvinyl chloride resin, nano-sized carbon 25 parts of sour calcium, 16 parts of acetone sodium, 21 parts of calcium stearate, 14 parts of ammonium polyphosphate, 13 parts, it is 18 parts of diaminodiphenyl-methane, poly- 13 parts of vinyl formal, 16 parts of 2-4 dihydroxy benaophenonels,(1)The parts by weight for weighing each material in embodiment 3, will be swollen Moisten soil, white carbon, crosslinked polyethylene, glass fibre, polyvinyl chloride resin, nano-calcium carbonate, acetone sodium, calcium stearate, polyphosphoric acids Ammonium, diaminodiphenyl-methane, polyvinyl formal, 2-4 dihydroxy benaophenonels, which are put into mixer, carries out mixing mixing, Smelting temperature is 70-85 DEG C, mixing time 30min;(2)The material obtained in step 2 is subjected to vulcanizing treatment, curing temperature It is 150-170 DEG C, vulcanization time 15min;(3)The material that step 3 is obtained carries out mill processing, mixing temperature with open mill It is 50-65 DEG C;(4)It by the materials result obtained in step 4, opens item and is cooled to room temperature, obtain finished product.
Comparative example 4
Weigh 25 parts of bentonite, 15 parts of white carbon, 10 parts of crosslinked polyethylene, 10 parts of glass fibre, 8 parts of polyvinyl chloride resin, nano-calcium carbonate 15 parts of calcium, 10 parts of acetone sodium, 14 parts of calcium stearate, 8 parts of ammonium polyphosphate,(1)Weigh the parts by weight of each material in embodiment 2 Number, by bentonite, white carbon, crosslinked polyethylene, glass fibre, polyvinyl chloride resin, nano-calcium carbonate, acetone sodium, calcium stearate, more Ammonium polyphosphate, which is put into mixer, carries out mixing mixing, and smelting temperature is 70-85 DEG C, mixing time 30min;(2)By step 2 In obtained material carry out vulcanizing treatment, curing temperature is 150-170 DEG C, vulcanization time 15min;(3)Step 3 is obtained Material carries out mill processing with open mill, and mixing temperature is 50-65 DEG C;(4)By the materials result obtained in step 4, to open item cold But to room temperature, finished product is obtained.
Embodiment 1-3 and comparative example 1-4 is respectively adopted and prepares cable cover(ing), measured data such as the following table 1:
Tensile strength(M/Pa) Elongation at break(%) Tensile strength(M/Pa) Dielectric strength(V/m) Oxygen index (OI)(%)
Embodiment 1 25.3 620 14.4 35 38
Embodiment 2 26.1 617 16.1 34 37
Embodiment 3 24.8 610 13.8 32 39
Comparative example 1 19.8 550 9.1 26 27
Comparative example 2 20.2 513 8.5 27 28
Comparative example 3 21.1 520 8.4 25 29
Comparative example 4 17.3 450 6.3 21 21
Ozone resistance test
Cable cover(ing) is made in material in embodiment 1-3 and comparative example 1-4, ozone resistance test, examination are carried out after the completion of preparing The condition of testing is:It it is 25-30 DEG C, testing time 48h in temperature, ozone concentration is 0.035 ~ 0.045%, test result such as following table 2:
Embodiment 1 Embodiment 2 Embodiment 3 Comparative example 1 Comparative example 2 Comparative example 3 Comparative example 4
Ozone resistance test Without cracking Without cracking Without cracking Cracking Cracking Cracking Cracking
By the data of Tables 1 and 2:There can be preferable uvioresistant by cable jacket material obtained in this patent Line ability and toughness, are exposed in air for a long time, situation that will not be cracking because of long-term illuminated ultraviolet light, extend The service life of cable facilitates the use of people.
The above is the embodiment of the present invention, therefore all structure, feature and principles according to described in the present patent application range are done Equivalent change or modification, be included within the scope of present patent application.

Claims (5)

1. antiultraviolet stable type cable jacket material is worn in a kind of resistance, which is characterized in that by below according to the raw material of parts by weight Composition:10-40 parts of bentonite, 5-25 parts of white carbon, 4-16 parts of crosslinked polyethylene, 5-15 parts of glass fibre, polyvinyl chloride resin 3-13 Part, 5-25 parts of nano-calcium carbonate, 2-14 parts of modified epoxy, 4-16 parts of acetone sodium, 7-21 parts of calcium stearate, ammonium polyphosphate 2-14 parts, 3-13 parts of diethyl amino propylamine, 4-18 parts of diaminodiphenyl-methane, 3-13 parts of polyvinyl formal, 2-4 dihydroxies 4-16 parts of base benzophenone,
The preparation method of the modified epoxy is as follows:
Epoxy resin is heated in a kettle, heating time 60-120min, poly- second is added after the completion of heating Alkene, dibasic lead stearate, phosphorus curing agent and diethylenetriamine, are stirred again, and mixing time 80min is stirred It is passed through nitrogen after the completion of mixing, silane coupling agent is added in a nitrogen environment, fully carries out stewing process after reaction, obtains modified ring Oxygen resin.
2. antiultraviolet stable type cable jacket material is worn in a kind of resistance according to claim 1, which is characterized in that by following It is formed according to the raw material of parts by weight:10-35 parts of bentonite, 5-20 parts of white carbon, 4-14 parts of crosslinked polyethylene, glass fibre 5- 13 parts, 3-11 parts of polyvinyl chloride resin, 5-22 parts of nano-calcium carbonate, 2-12 parts of modified epoxy, 4 parts of acetone sodium 4-1, calcium stearate 7-19 parts, 2-12 parts of ammonium polyphosphate, 3-11 parts of diethyl amino propylamine, 4-16 parts of diaminodiphenyl-methane, polyvinyl alcohol contracting 3-11 parts of formaldehyde, 4-14 parts of 2-4 dihydroxy benaophenonels.
3. antiultraviolet stable type cable jacket material is worn in a kind of resistance according to claim 1, which is characterized in that by following It is formed according to the raw material of parts by weight:25 parts of bentonite, 15 parts of white carbon, 10 parts of crosslinked polyethylene, 10 parts of glass fibre, PVC 8 parts of resin, 15 parts of nano-calcium carbonate, 8 parts of modified epoxy, 10 parts of acetone sodium, 14 parts of calcium stearate, 8 parts of ammonium polyphosphate, 8 parts of diethyl amino propylamine, 11 parts of diaminodiphenyl-methane, 8 parts of polyvinyl formal, 10 parts of 2-4 dihydroxy benaophenonels.
4. the preparation method of antiultraviolet stable type cable jacket material is worn according to a kind of any resistances of claim 1-3, It is characterized in that, comprising the steps of:
The parts by weight for weighing each material in claim 3, by bentonite, white carbon, crosslinked polyethylene, glass fibre, PVC trees Fat, nano-calcium carbonate, acetone sodium, calcium stearate, ammonium polyphosphate, diethyl amino propylamine, diaminodiphenyl-methane, polyethylene Alcohol formal, 2-4 dihydroxy benaophenonels, which are put into mixer, carries out mixing mixing, and smelting temperature is 70-85 DEG C, mixing time For 30min;
Modified epoxy will be added in the material obtained in step 1, adjust mixer temperature, mixer temperature is 80-95 DEG C, Mixing mixing time is 20min, obtains blend glue stuff;
The material obtained in step 2 is subjected to vulcanizing treatment, curing temperature is 150-170 DEG C, vulcanization time 15min;
The material that step 3 is obtained carries out mill processing with open mill, and mixing temperature is 50-65 DEG C;
It by the materials result obtained in step 4, opens item and is cooled to room temperature, obtain finished product.
5. antiultraviolet stable type cable jacket material is worn in a kind of resistance according to claim 1, it is characterised in that:Described two 11 parts of aminodiphenylmethane, 8 parts of polyvinyl formal, 2-4 dihydroxy benaophenonel materials weight part ratio be 1:2: 1。
CN201810300087.2A 2018-04-04 2018-04-04 Antiultraviolet stable type cable jacket material and preparation method thereof is worn in a kind of resistance Withdrawn CN108641203A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109180106A (en) * 2018-10-13 2019-01-11 孙浩 A kind of construction material and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109180106A (en) * 2018-10-13 2019-01-11 孙浩 A kind of construction material and preparation method thereof

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