CN112812420A - Low-smoke halogen-free cable material containing novel functional compatilizer and preparation thereof - Google Patents

Low-smoke halogen-free cable material containing novel functional compatilizer and preparation thereof Download PDF

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CN112812420A
CN112812420A CN202110139222.1A CN202110139222A CN112812420A CN 112812420 A CN112812420 A CN 112812420A CN 202110139222 A CN202110139222 A CN 202110139222A CN 112812420 A CN112812420 A CN 112812420A
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compatilizer
cable material
halogen
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CN112812420B (en
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崔曾涛
崔增波
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Langfang Cui's Cable Materials Co ltd
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Langfang Cui's Cable Materials Co ltd
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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
    • C08L23/02Compositions 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
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • C08L23/0846Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
    • C08L23/0853Vinylacetate
    • 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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    • C08L2201/00Properties
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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    • C08L2201/00Properties
    • C08L2201/08Stabilised against heat, light or radiation or oxydation
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    • C08L2203/00Applications
    • C08L2203/20Applications use in electrical or conductive gadgets
    • C08L2203/202Applications use in electrical or conductive gadgets use in electrical wires or wirecoating
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    • 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
    • CCHEMISTRY; METALLURGY
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    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/08Polymer mixtures characterised by other features containing additives to improve the compatibility between two polymers

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Abstract

The invention relates to a low-smoke halogen-free cable material containing a novel functional compatilizer and a preparation method thereof, wherein the cable material is prepared from the following raw materials in parts by weight: 50-60 parts of ethylene-vinyl acetate copolymer, 20-40 parts of fluorosilicone rubber, 10-20 parts of terpene resin, 15-30 parts of polyphenyl ether resin, 6-15 parts of functional compatilizer, 50-70 parts of halogen-free flame retardant, 5-10 parts of reinforcing agent, 2-6 parts of peroxide cross-linking agent, 3-9 parts of stabilizer, 0.5-1 part of lubricant and 0.2-1 part of antioxidant. Compared with the prior art, the cable material disclosed by the invention is simple in preparation process, has good molding processability and physical and mechanical properties, is resistant to oil stain, heat, cold and aging, water, acid and alkali, and chemical reagents, has excellent electrical insulation and heat-resistant flame retardance, ensures the working performance and the service life of the cable, greatly improves the safety and the reliability of the cable in use, and can realize industrial production.

Description

Low-smoke halogen-free cable material containing novel functional compatilizer and preparation thereof
Technical Field
The invention belongs to the technical field of wires and cables, and relates to a low-smoke halogen-free cable material containing a novel functional compatilizer and a preparation method thereof.
Background
Along with the rapid development of economic construction, the living standard of people is continuously improved, and the demand for various cables is more and more increased due to the rapid development of various infrastructures in cities and countryside, and the cables are carriers of power transmission, are the foundation for ensuring the normal work of electric products, and play the roles of transmitting power, transmitting information and realizing electromagnetic energy conversion in the electric products. The cable material is a necessary material for preparing the cable, and the performance of the cable material directly influences the transmission quality of various energies and signals and the service life of the cable.
The existing conventional cable materials on the market have poor weather resistance, when equipment is in outdoor work or is always placed in the atmosphere and is irradiated by solar ultraviolet rays for a long time, the surface of the equipment is cracked, and connecting wires of some equipment or automobiles are in direct contact with mineral oil such as gasoline, engine oil and the like, so that the surface swelling phenomenon is easy to occur, the physical and mechanical properties of the product are greatly reduced, and the cable materials have more potential risks in the using process and directly influence the property safety and personal safety of electronic and electrical equipment, automobiles and the like. In particular, the short circuit of the cable in some large-scale electronic and electric equipment is easy to burn out the electric equipment, and a fire disaster can happen in serious conditions. When the working environment is high, the phenomena of melting, dry cracking and the like can occur, the insulating function is lost, the cable becomes soft under the long-time high-power use state, and the mechanical property is poor. In addition, in the practical application process, the electric wire and the electric cable can be bent along with the movement of the electric wire and the electric cable, the electric wire and the electric cable are frequently inserted and pulled out, the electric wire and the electric cable are not good in flexibility and can be broken when being used for a long time, and the phenomenon is more obvious particularly in a high-temperature working occasion.
Disclosure of Invention
The invention aims to overcome the defects in the prior art and provide a low-smoke halogen-free cable material containing a novel functional compatilizer, which is convenient to form and process, better in weather resistance, water erosion resistance, flame retardance, high-temperature resistance and environmental protection performance and longer in service life, and a preparation method thereof.
The purpose of the invention can be realized by the following technical scheme:
according to one aspect of the invention, the low-smoke halogen-free cable material containing the novel functional compatilizer is prepared from the following raw materials in parts by weight: 50-60 parts of ethylene-vinyl acetate copolymer, 20-40 parts of fluorosilicone rubber, 10-20 parts of terpene resin, 15-30 parts of polyphenyl ether resin, 6-15 parts of functional compatilizer, 50-70 parts of halogen-free flame retardant, 5-10 parts of reinforcing agent, 2-6 parts of peroxide cross-linking agent, 3-9 parts of stabilizer, 0.5-1 part of lubricant and 0.2-1 part of antioxidant.
In one embodiment, the ethylene-vinyl acetate copolymer has a vinyl acetate content of 12 to 25wt% and a melt index of 8 to 20 g/10min (190 ℃, 2.16 kg).
In one embodiment, the fluorosilicone rubber has a decrease in tensile strength at 225 ℃ for 72 hours of not more than 35% from its initial tensile strength and a decrease in elongation at break of not more than 30% from its initial elongation at break.
Preferably, the fluorosilicone rubber may be selected from the commercially available FSR8430-U, FSR8440-U, FSR8460-U, FSR 8470-U.
In one embodiment, the softening point of the terpene resin is 100-130 ℃, and the acid value of the terpene resin is less than 1.0 mg KOH/g.
Preferably, the terpene resin may be selected from one or more of commercially available TP1105, TP1115 or TP 1125.
In one embodiment, the polyphenylene ether resin has a molding shrinkage of 0.7% or less and a volume resistivity of 1000 Ω & cm or more at 23 ℃ and a relative humidity of 50%.
Preferably, the polyphenylene ether resin is available from 540Z, manufactured by asahi.
As an embodiment, the functional compatilizer is prepared by compounding the following components in parts by weight: 70-90 parts of maleic anhydride grafted hydrogenated styrene-butadiene-styrene block copolymer, 10-30 parts of siloxane copolymer, 15-30 parts of modified kaolin and 2-8 parts of alicyclic amine activator.
As an embodiment, the modified kaolin is prepared by: mixing kaolin powder and absolute ethyl alcohol uniformly to prepare a mixed solution of the kaolin powder and the absolute ethyl alcohol; adding hydroxymethyl cellulose, a silane coupling agent and calcium sulfate whiskers into the mixed solution, adjusting the pH of the solution to 5 by using dilute nitric acid, reacting for 2-4 hours at 60-72 ℃, cooling, filtering, washing, drying to constant weight, grinding, and sieving with a 1000-mesh sieve.
Preferably, the kaolin powder and the absolute ethyl alcohol are in the following dosage relation: 10-20 g of kaolin powder is added into each 100 mL of absolute ethyl alcohol, the dosage of the hydroxymethyl cellulose is 10-15% of the mass of the kaolin powder, the dosage of the silane coupling agent is 2-5% of the mass of the kaolin powder, and the dosage of the calcium sulfate whisker is 1-3% of the mass of the kaolin powder.
Preferably, the maleic anhydride grafted hydrogenated styrene-butadiene-styrene block copolymer is available from Kraton FG 1901, shell company, usa.
Preferably, the siloxane copolymer is selected from one or more of polyimide siloxane, polyetherimide sulfone siloxane, polysulfone siloxane, polyether sulfone siloxane or polyphenylene ether siloxane.
Preferably, the cycloaliphatic amine activator is selected from triethylenediamine, hexamethylenetetramine or diethylenetriamine.
The functional compatilizer can be prepared by the following method: the raw material components are added into a double-screw extruder according to the parts by weight, and are extruded and granulated at the temperature of 230 ℃ and 250 ℃.
As an embodiment, the halogen-free flame retardant is a phosphorus-containing flame retardant, and may be selected from one or more of triphenyl phosphate, tricresyl phosphate, cresyl diphenyl phosphate, ditolyl phosphate, tris (2,4, 6-trimethylphenyl) phosphate, tris (2, 4-di-t-butylphenyl) phosphate, tris (2, 6-di-t-butylphenyl) phosphate, resorcinol bis (diphenyl phosphate), hydroquinone bis (diphenyl phosphate), bisphenol A-bis (diphenyl phosphate), resorcinol bis (2, 6-di-t-butylphenyl phosphate), hydroquinone bis (2, 6-dimethylphenyl phosphate).
As an embodiment, the reinforcing agent is fumed silica.
As an embodiment, the peroxide crosslinking agent is selected from one or more of bis (4-methylbenzoyl) peroxide, tert-butyl peroxy-2-ethylhexyl carbonate or 1, 1-bis (tert-butyl peroxy) cyclohexane.
In one embodiment, the stabilizer is an organotin-based heat stabilizer and may be selected from at least one of dibutyltin maleate, dibutyltin dilaurate, dibutyltin laurate maleate, di-n-octyltin dilaurate, or di-n-octyltin bis (isooctyl thioglycolate).
As an embodiment, the lubricant is at least one of natural paraffin, liquid paraffin, microcrystalline paraffin, polyethylene wax, butyl stearate, oleamide, ethylene bis stearamide, or silicone powder.
In one embodiment, the antioxidant is at least one of 2, 6-di-tert-butyl-p-cresol, octadecyl beta (3, 5-di-tert-butyl-4-hydroxyphenyl) propionate, 1,3 tris (2-methyl-4-hydroxy-5-tert-butylphenyl) butane, 2 ' -methylenebis (4-ethyl-6-tert-butylphenol), 1,3, 5-tris (3, 5-tert-butyl-4-hydroxybenzyl) trimethylbenzene, 2 ' -methylenebis (4-methyl-6-tert-butylphenol), 4 ' -di-tert-octyldiphenylamine.
According to another aspect of the present invention, there is provided a preparation method of the low smoke zero halogen cable material containing the novel functional compatibilizer, which includes the following steps:
step 1): uniformly stirring and mixing ethylene-vinyl acetate copolymer, polyphenyl ether resin, a functional compatilizer, a halogen-free flame retardant, a peroxide crosslinking agent, a stabilizer, a lubricant and an antioxidant in parts by weight at a high speed to prepare a premix A;
step 2): uniformly stirring and mixing the fluorosilicone rubber, the terpene resin and the reinforcing agent at a high speed according to the parts by weight to prepare a premix B;
step 3): adding the premix A into a double-screw extruder from a main feed inlet, adding the premix B into the double-screw extruder through a side feed inlet, and cooling, drying and granulating after extrusion to obtain the low-smoke halogen-free cable material.
As a preferred technical scheme, the temperature of the first zone of the double-screw extruder is 210-230 ℃, the temperature of the second zone is 220-240 ℃, the temperature of the third zone is 220-240 ℃, the temperature of the fourth zone is 220-240 ℃, the temperature of the fifth zone is 230-250 ℃, the temperature of the sixth zone is 240-260 ℃, the temperature of the seventh zone is 230-250 ℃, the temperature of the eighth zone is 220-240 ℃ and the temperature of the ninth zone is 200-220 ℃.
Compared with the prior art, the invention has the following characteristics:
1) the cable material of the invention takes ethylene-vinyl acetate copolymer as a main substrate, introduces fluorosilicone rubber to enhance the toughness and weather aging resistance of the substrate, is favorable for improving the medium resistance of the substrate due to the fact that the fluorosilicone rubber carries fluorine-containing groups, can improve the tolerance of a material system to organic solvents, oil substances and acid and alkali substances, and has stronger interaction aiming at the fluorosilicone rubber, the molecular main chain structural unit of the fluorosilicone rubber is-Si-O-, and gas-phase white carbon black is taken as a reinforcing agent, the fluorosilicone rubber and the gas-phase white carbon black have the same silica framework, the gas-phase white carbon black particles can be stably filled in the gaps of a cross-linked network in the fluorosilicone rubber, so that the strength of the fluorosilicone rubber can be enhanced, the fluorosilicone rubber can be taken as a carrier and dispersed in the ethylene-vinyl acetate copolymer substrate, and the heat resistance and the resistance of the substrate can, the final material has excellent electrical insulation and flame retardance, and the terpene resin is compounded with the fluorosilicone rubber, so that the adhesion between the fluorosilicone rubber particles and the base material is enhanced, the fluorosilicone rubber can be stably fused in the base material, and the aging resistance of the base material can be further improved;
2) the functional compatilizer is prepared by adopting maleic anhydride grafted hydrogenated styrene-butadiene-styrene block copolymer, siloxane copolymer, modified kaolin and alicyclic amine activator through extrusion granulation, wherein the modified kaolin is prepared by adopting silane coupling agent to graft hydroxymethyl cellulose onto the surface of kaolin particles, and the modified kaolin particles can be grafted with the maleic anhydride grafted hydrogenated styrene-butadiene-styrene block copolymer, the alicyclic amine activator under the action of the alicyclic amine activator, The siloxane copolymer forms a strong chemical bond, so that a cross-linked network is formed between the maleic anhydride grafted hydrogenated styrene-butadiene-styrene block copolymer and the siloxane copolymer, and the two can be stably combined together to form a composite carrier, which is not only beneficial to reducing the size of dispersed particles of the modified kaolin so that the modified kaolin is uniformly and stably dispersed in the base resin to improve the volume resistivity and the heat-resistant flame retardance of a material system, but also capable of reducing the interfacial tension between the ethylene-vinyl acetate copolymer, the fluorosilicone rubber and the polyphenyl ether resin to increase the compatibility among the three, so that the dispersed phase and the continuous phase are uniformly stabilized, and the processing rheological property of the material system is improved;
3) the cable material disclosed by the invention is simple in preparation process, has good molding processability and physical and mechanical properties, is resistant to oil stain, heat, cold, aging, water, acid and alkali, and chemical reagents, has excellent electrical insulation and heat-resistant flame retardance, ensures the working performance and the service life of the cable, greatly improves the safety and the reliability of the cable in use, and can realize industrial production.
Detailed Description
The technical solutions of the present invention will be described clearly and completely with reference to specific embodiments, and it should be understood that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. The present embodiment is implemented on the premise of the technical solution of the present invention, and a detailed embodiment and a specific operation process are given, but the scope of the present invention is not limited to the following embodiments. All other embodiments obtained by a person skilled in the art without making any inventive step are within the scope of protection of the present invention.
As used herein, the term "about" when used to modify a numerical value means within + -5% of the error margin measured for that value.
The theory or mechanism described and disclosed herein, whether correct or incorrect, should not limit the scope of the present invention in any way, i.e., the present disclosure may be practiced without limitation to any particular theory or mechanism.
The present invention will be described in detail with reference to specific examples.
Example 1:
the low-smoke halogen-free cable material is prepared from the following raw materials in parts by weight: 50 parts of ethylene-vinyl acetate copolymer, 20 parts of fluorosilicone rubber, 10 parts of terpene resin, 15 parts of polyphenyl ether resin, 6 parts of functional compatilizer, 50 parts of halogen-free flame retardant, 5 parts of reinforcing agent, 2 parts of peroxide cross-linking agent, 3 parts of stabilizer, 0.5 part of lubricant and 0.2 part of antioxidant.
Wherein the ethylene-vinyl acetate copolymer has a vinyl acetate content of 12 wt% and a melt index of about 8 g/10min (190 deg.C, 2.16 kg); the fluorosilicone rubber used is FSR8430-U sold in the market; the terpene resin used was commercially available TP 1105; the polyphenylene ether resin has a molding shrinkage of 0.7% or less, a volume resistivity of 1000 Ω -cm at 23 deg.C and 50% relative humidity, and is available from 540Z available from Asahi Kasei K.K.; the halogen-free flame retardant is triphenyl phosphate; the reinforcing agent is fumed silica; the peroxide crosslinking agent is di (4-methylbenzoyl) peroxide; the stabilizer is dibutyltin maleate; the used lubricant is natural paraffin; the antioxidant is prepared by mixing 2, 6-di-tert-butyl-p-cresol and 4, 4' -di-tert-octyldiphenylamine in a mass ratio of 4: 1.
The functional compatilizer in the embodiment is prepared by compounding the following components in parts by weight: 70 parts of maleic anhydride grafted hydrogenated styrene-butadiene-styrene block copolymer, 10 parts of siloxane copolymer, 15 parts of modified kaolin and 2 parts of alicyclic amine activator; of these, the maleic anhydride grafted hydrogenated styrene-butadiene-styrene block copolymer was obtained from Kraton FG 1901, shell, usa, and the siloxane copolymer was a polyimide siloxane and the alicyclic amine activator was triethylenediamine.
The preparation method of the modified kaolin used in the functional compatilizer comprises the following steps: mixing kaolin powder and absolute ethyl alcohol uniformly to prepare a mixed solution of the kaolin powder and the absolute ethyl alcohol; adding hydroxymethyl cellulose, a silane coupling agent and calcium sulfate whiskers into the mixed solution, adjusting the pH of the solution to 5 by using dilute nitric acid, reacting for 4 hours at 60 ℃, cooling, filtering, washing, drying to constant weight, grinding, and sieving with a 1000-mesh sieve.
In the preparation method, the dosage relationship between the kaolin powder and the absolute ethyl alcohol is as follows: every 100 mL of absolute ethyl alcohol is added with 10 g of kaolin powder, the dosage of hydroxymethyl cellulose is 10 percent of the mass of the kaolin powder, the dosage of silane coupling agent is 2 percent of the mass of the kaolin powder, and the dosage of calcium sulfate whisker is 1 percent of the mass of the kaolin powder.
Based on the raw materials of each component of the functional compatilizer, the raw materials are added into a double-screw extruder according to the parts by weight, and are extruded and granulated at 230 ℃ to obtain the functional compatilizer.
Example 2:
the low-smoke halogen-free cable material is prepared from the following raw materials in parts by weight: 60 parts of ethylene-vinyl acetate copolymer, 40 parts of fluorosilicone rubber, 20 parts of terpene resin, 30 parts of polyphenyl ether resin, 15 parts of functional compatilizer, 70 parts of halogen-free flame retardant, 10 parts of reinforcing agent, 6 parts of peroxide cross-linking agent, 9 parts of stabilizer, 1 part of lubricant and 1 part of antioxidant.
Wherein the ethylene-vinyl acetate copolymer used has a vinyl acetate content of 25wt% and a melt index of about 20 g/10min (190 ℃, 2.16 kg); the fluorosilicone rubber used is FSR8440-U which is commercially available; the terpene resin used was commercially available TP 1115; the polyphenylene ether resin has a molding shrinkage of 0.7% or less, a volume resistivity of 1000 Ω -cm at 23 deg.C and 50% relative humidity, and is available from 540Z available from Asahi Kasei K.K.; the halogen-free flame retardant is prepared by mixing cresyl diphenyl phosphate and tri (2,4, 6-trimethylphenyl) phosphate according to the mass ratio of 1: 1; the reinforcing agent is fumed silica; the peroxide crosslinking agent is di (4-methylbenzoyl) peroxide; the stabilizer used is dibutyltin dilaurate; the lubricant used was butyl stearate; the antioxidant used was octadecyl beta (3,5 di-tert-butyl-4-hydroxyphenyl) propionate.
The functional compatilizer in the embodiment is prepared by compounding the following components in parts by weight: 90 parts of maleic anhydride grafted hydrogenated styrene-butadiene-styrene block copolymer, 30 parts of siloxane copolymer, 30 parts of modified kaolin and 8 parts of alicyclic amine activator; among them, maleic anhydride grafted hydrogenated styrene-butadiene-styrene block copolymer was purchased from Kraton FG 1901, shell company, usa, the siloxane copolymer was polyetherimide siloxane, and the alicyclic amine activator was hexamethylenetetramine.
The preparation method of the modified kaolin used in the functional compatilizer comprises the following steps: mixing kaolin powder and absolute ethyl alcohol uniformly to prepare a mixed solution of the kaolin powder and the absolute ethyl alcohol; adding hydroxymethyl cellulose, a silane coupling agent and calcium sulfate whiskers into the mixed solution, adjusting the pH of the solution to 5 by using dilute nitric acid, reacting for 2 hours at 72 ℃, cooling, filtering, washing, drying to constant weight, grinding, and sieving with a 1000-mesh sieve.
In the preparation method, the dosage relationship between the kaolin powder and the absolute ethyl alcohol is as follows: every 100 mL of absolute ethyl alcohol is added with 20 g of kaolin powder, the dosage of hydroxymethyl cellulose is 15 percent of the mass of the kaolin powder, the dosage of silane coupling agent is 5 percent of the mass of the kaolin powder, and the dosage of calcium sulfate whisker is 3 percent of the mass of the kaolin powder.
Based on the raw materials of each component of the functional compatilizer, the raw materials are added into a double-screw extruder according to the parts by weight, and are extruded and granulated at 250 ℃ to obtain the functional compatilizer.
Example 3:
the low-smoke halogen-free cable material is prepared from the following raw materials in parts by weight: 54 parts of ethylene-vinyl acetate copolymer, 32 parts of fluorosilicone rubber, 14 parts of terpene resin, 20 parts of polyphenyl ether resin, 10 parts of functional compatilizer, 56 parts of halogen-free flame retardant, 6 parts of reinforcing agent, 4 parts of peroxide cross-linking agent, 4 parts of stabilizer, 0.6 part of lubricant and 0.4 part of antioxidant.
Wherein the ethylene-vinyl acetate copolymer has a vinyl acetate content of 18 wt% and a melt index of about 11 g/10min (190 deg.C, 2.16 kg); the fluorosilicone rubber used is FSR8460-U which is sold on the market; the terpene resin used was commercially available TP 1125; the polyphenylene ether resin has a molding shrinkage of 0.7% or less, a volume resistivity of 1000 Ω -cm at 23 deg.C and 50% relative humidity, and is available from 540Z available from Asahi Kasei K.K.; the used halogen-free flame retardant is hydroquinone bis (2, 6-dimethylphenyl phosphate); the reinforcing agent is fumed silica; the peroxide crosslinking agent is tert-butyl peroxy-2-ethylhexyl carbonate; the stabilizer is prepared by mixing dibutyltin laurate maleate and di (isooctyl thioglycolate) di-n-octyl tin according to the mass ratio of 9: 1; the lubricant is prepared by mixing natural paraffin, polyethylene wax and ethylene bis stearamide according to the mass ratio of 1:1: 3; the antioxidant used was 2, 2' -methylenebis (4-methyl-6-tert-butylphenol).
The functional compatilizer in the embodiment is prepared by compounding the following components in parts by weight: 82 parts of maleic anhydride grafted hydrogenated styrene-butadiene-styrene block copolymer, 18 parts of siloxane copolymer, 25 parts of modified kaolin and 5 parts of alicyclic amine activator; the maleic anhydride grafted hydrogenated styrene-butadiene-styrene block copolymer is obtained from Kraton FG 1901 of Shell company of America, the siloxane copolymer is polyetherimide sulfone siloxane, and the alicyclic amine activator is formed by mixing hexamethylenetetramine and diethylenetriamine according to the mass ratio of 1: 1.
The preparation method of the modified kaolin used in the functional compatilizer comprises the following steps: mixing kaolin powder and absolute ethyl alcohol uniformly to prepare a mixed solution of the kaolin powder and the absolute ethyl alcohol; adding hydroxymethyl cellulose, a silane coupling agent and calcium sulfate whiskers into the mixed solution, adjusting the pH of the solution to 5 by using dilute nitric acid, reacting for 3 hours at 68 ℃, cooling, filtering, washing, drying to constant weight, grinding, and sieving with a 1000-mesh sieve.
In the preparation method, the dosage relationship between the kaolin powder and the absolute ethyl alcohol is as follows: every 100 mL of absolute ethyl alcohol is added with 15 g of kaolin powder, the dosage of hydroxymethyl cellulose is 12 percent of the mass of the kaolin powder, the dosage of silane coupling agent is 4 percent of the mass of the kaolin powder, and the dosage of calcium sulfate whisker is 2 percent of the mass of the kaolin powder.
Based on the raw materials of each component of the functional compatilizer, the raw materials are added into a double-screw extruder according to the parts by weight, and are extruded and granulated at 250 ℃ to obtain the functional compatilizer.
Example 4:
the low-smoke halogen-free cable material is prepared from the following raw materials in parts by weight: 58 parts of ethylene-vinyl acetate copolymer, 27 parts of fluorosilicone rubber, 12 parts of terpene resin, 23 parts of polyphenyl ether resin, 9 parts of functional compatilizer, 52 parts of halogen-free flame retardant, 7 parts of reinforcing agent, 4 parts of peroxide crosslinking agent, 8 parts of stabilizer, 0.7 part of lubricant and 0.8 part of antioxidant.
Wherein the ethylene-vinyl acetate copolymer used has a vinyl acetate content of 22 wt% and a melt index of about 18 g/10min (190 ℃, 2.16 kg); the fluorosilicone rubber used is FSR8470-U sold in the market; the terpene resin used was commercially available TP 1125; the polyphenylene ether resin has a molding shrinkage of 0.7% or less, a volume resistivity of 1000 Ω -cm at 23 deg.C and 50% relative humidity, and is available from 540Z available from Asahi Kasei K.K.; the used halogen-free flame retardant is resorcinol bis (2, 6-di-tert-butyl phenyl phosphate); the reinforcing agent is fumed silica; the peroxide crosslinking agent used is 1, 1-di (tert-butylperoxy) cyclohexane; the stabilizer used is di-n-octyltin dilaurate; the lubricant is formed by mixing microcrystalline paraffin, oleamide and silicone powder according to the mass ratio of 1:1: 1; the antioxidant used was 1,3, 5-tris (3, 5-tert-butyl-4-hydroxybenzyl) trimethylbenzene.
The functional compatilizer in the embodiment is prepared by compounding the following components in parts by weight: 76 parts of maleic anhydride grafted hydrogenated styrene-butadiene-styrene block copolymer, 24 parts of siloxane copolymer, 26 parts of modified kaolin and 4 parts of alicyclic amine activator; the maleic anhydride grafted hydrogenated styrene-butadiene-styrene block copolymer is obtained from Kraton FG 1901 of Shell company of America, the siloxane copolymer is prepared by mixing polyphenylene ether siloxane and polysulfone siloxane according to the mass ratio of 4:1, and the alicyclic amine activator is triethylene diamine.
The preparation method of the modified kaolin used in the functional compatilizer comprises the following steps: mixing kaolin powder and absolute ethyl alcohol uniformly to prepare a mixed solution of the kaolin powder and the absolute ethyl alcohol; adding hydroxymethyl cellulose, a silane coupling agent and calcium sulfate whiskers into the mixed solution, adjusting the pH of the solution to 5 by using dilute nitric acid, reacting for 4 hours at 65 ℃, cooling, filtering, washing, drying to constant weight, grinding, and sieving with a 1000-mesh sieve.
In the preparation method, the dosage relationship between the kaolin powder and the absolute ethyl alcohol is as follows: adding 18 g of kaolin powder into each 100 mL of absolute ethyl alcohol, wherein the dosage of the hydroxymethyl cellulose is 14% of the mass of the kaolin powder, the dosage of the silane coupling agent is 5% of the mass of the kaolin powder, and the dosage of the calcium sulfate whisker is 2% of the mass of the kaolin powder.
Based on the raw materials of each component of the functional compatilizer, the raw materials are added into a double-screw extruder according to the parts by weight, and are extruded and granulated at 250 ℃ to obtain the functional compatilizer.
The cable materials of the above examples 1-4 were prepared by the following method:
step 1): uniformly stirring and mixing ethylene-vinyl acetate copolymer, polyphenyl ether resin, a functional compatilizer, a halogen-free flame retardant, a peroxide crosslinking agent, a stabilizer, a lubricant and an antioxidant in parts by weight at a high speed to prepare a premix A;
step 2): uniformly stirring and mixing the fluorosilicone rubber, the terpene resin and the reinforcing agent at a high speed according to the parts by weight to prepare a premix B;
step 3): adding the premix A into a double-screw extruder from a main feed inlet, adding the premix B into the double-screw extruder through a side feed inlet, cooling, drying and granulating after extrusion to obtain the low-smoke halogen-free cable material.
In the preparation method, the temperature of the first zone of the double-screw extruder is 230 ℃, the temperature of the second zone is 235 ℃, the temperature of the third zone is 240 ℃, the temperature of the fourth zone is 240 ℃, the temperature of the fifth zone is 250 ℃, the temperature of the sixth zone is 260 ℃, the temperature of the seventh zone is 252 ℃, the temperature of the eighth zone is 240 ℃ and the temperature of the ninth zone is 220 ℃.
Comparative example 1:
the comparative example cable material was Kraton FG 1901 as a compatibilizer as in example 3.
Comparative example 2:
this comparative example does not contain fluorosilicone rubber, terpene resin, and reinforcing agent, as in example 3.
The results of the performance test of the cable materials prepared in examples 1 to 4 and comparative examples 1 to 2 are shown in table 1 below.
TABLE 1 test results
Figure DEST_PATH_IMAGE002
Note: the tensile strength and elongation at break tests in Table 1 were carried out in accordance with GB/T1040.3.
As can be seen from the test results in Table 1, the cable materials prepared in the embodiments 1-4 of the present invention have excellent mechanical strength, good water erosion resistance, outstanding flame retardancy and insulation properties, and good application prospects.
Although the present invention has been described in detail, modifications within the spirit and scope of the invention will be apparent to those skilled in the art. Furthermore, it should be understood that the various aspects recited, portions of different embodiments, and various features recited may be combined or interchanged either in whole or in part. In the various embodiments described above, those embodiments that refer to another embodiment may be combined with other embodiments as appropriate, as will be appreciated by those skilled in the art. Furthermore, those skilled in the art will appreciate that the foregoing description is by way of example only, and is not intended to limit the invention.

Claims (10)

1. A low-smoke halogen-free cable material containing a novel functional compatilizer is characterized by being prepared from the following raw materials in parts by weight: 50-60 parts of ethylene-vinyl acetate copolymer, 20-40 parts of fluorosilicone rubber, 10-20 parts of terpene resin, 15-30 parts of polyphenyl ether resin, 6-15 parts of functional compatilizer, 50-70 parts of halogen-free flame retardant, 5-10 parts of reinforcing agent, 2-6 parts of peroxide cross-linking agent, 3-9 parts of stabilizer, 0.5-1 part of lubricant and 0.2-1 part of antioxidant.
2. The low smoke zero halogen cable material containing the novel functional compatilizer according to claim 1, wherein the ethylene-vinyl acetate copolymer has a vinyl acetate content of 12-25wt% and a melt index of 8-20 g/10min (190 ℃, 2.16 kg).
3. The low smoke zero halogen cable material containing the novel functional compatilizer as claimed in claim 1, wherein the tensile strength of said fluorosilicone rubber at 225 ℃ for 72 hours is not more than 35% less than its initial tensile strength, and the elongation at break is not more than 30% less than its initial elongation at break.
4. The low-smoke halogen-free cable material containing the novel functional compatilizer according to claim 1, wherein the molding shrinkage rate of the polyphenylene ether resin is less than or equal to 0.7%, and the volume resistivity of the polyphenylene ether resin is more than 1000 Ω -cm under the conditions of 23 ℃ and 50% of relative humidity.
5. The low-smoke halogen-free cable material containing the novel functional compatilizer according to claim 1, wherein the functional compatilizer is prepared by compounding the following components and raw materials in parts by weight: 70-90 parts of maleic anhydride grafted hydrogenated styrene-butadiene-styrene block copolymer, 10-30 parts of siloxane copolymer, 15-30 parts of modified kaolin and 2-8 parts of alicyclic amine activator.
6. The low-smoke halogen-free cable material containing the novel functional compatilizer according to claim 5, wherein the preparation method of the modified kaolin is as follows: mixing kaolin powder and absolute ethyl alcohol uniformly to prepare a mixed solution of the kaolin powder and the absolute ethyl alcohol; adding hydroxymethyl cellulose, a silane coupling agent and calcium sulfate whiskers into the mixed solution, adjusting the pH of the solution to 5 by using dilute nitric acid, reacting for 2-4 hours at 60-72 ℃, cooling, filtering, washing, drying to constant weight, grinding, and sieving with a 1000-mesh sieve.
7. The low-smoke halogen-free cable material containing the novel functional compatilizer according to claim 6, wherein the dosage relationship between the kaolin powder and the absolute ethyl alcohol is as follows: 10-20 g of kaolin powder is added into each 100 mL of absolute ethyl alcohol, the dosage of the hydroxymethyl cellulose is 10-15% of the mass of the kaolin powder, the dosage of the silane coupling agent is 2-5% of the mass of the kaolin powder, and the dosage of the calcium sulfate whisker is 1-3% of the mass of the kaolin powder.
8. The low smoke zero halogen cable material containing the novel functional compatilizer is characterized in that the siloxane copolymer is selected from one or more of polyimide siloxane, polyetherimide sulfone siloxane, polysulfone siloxane, polyether sulfone siloxane or polyphenylene ether siloxane;
the alicyclic amine activator is selected from triethylenediamine, hexamethylenetetramine or diethylenetriamine.
9. The low-smoke halogen-free cable material containing the novel functional compatibilizer according to claim 1, wherein the halogen-free flame retardant is a phosphorus-containing flame retardant, the reinforcing agent is fumed silica, the peroxide crosslinking agent is one or more of bis (4-methylbenzoyl) peroxide, tert-butylperoxy-2-ethylhexyl carbonate or 1, 1-bis (tert-butylperoxy) cyclohexane, the stabilizer is an organic tin heat stabilizer, the lubricant is at least one of natural paraffin, liquid paraffin, microcrystalline paraffin, polyethylene wax, butyl stearate, oleamide, ethylene bis stearamide and silicone powder, the antioxidant is 2, 6-di-tert-butyl-p-cresol, beta (3,5 di-tert-butyl-4-hydroxyphenyl) octadecyl propionate and 1,1,3 tris (2-methyl-4 hydroxy-5-t-butylphenyl) butane, 2 ' -methylenebis (4-ethyl-6-t-butylphenol), 1,3, 5-tris (3, 5-t-butyl-4-hydroxybenzyl) trimethylbenzene, 2 ' -methylenebis (4-methyl-6-t-butylphenol), and 4,4 ' -di-t-octyldiphenylamine.
10. The preparation method of the low-smoke halogen-free cable material containing the novel functional compatilizer according to any one of claims 1 to 9, characterized by comprising the following steps:
step 1): uniformly stirring and mixing ethylene-vinyl acetate copolymer, polyphenyl ether resin, a functional compatilizer, a halogen-free flame retardant, a peroxide crosslinking agent, a stabilizer, a lubricant and an antioxidant in parts by weight at a high speed to prepare a premix A;
step 2): uniformly stirring and mixing the fluorosilicone rubber, the terpene resin and the reinforcing agent at a high speed according to the parts by weight to prepare a premix B;
step 3): adding the premix A into a double-screw extruder from a main feed inlet, adding the premix B into the double-screw extruder through a side feed inlet, and cooling, drying and granulating after extrusion to obtain the low-smoke halogen-free cable material.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112641483A (en) * 2020-12-22 2021-04-13 江苏省中医药研究院 Automatic pressing hemostasis device after tooth extraction
CN116082785A (en) * 2023-04-10 2023-05-09 宏亮电缆有限公司 High-temperature-resistant mining cable of stranded copper conductor

Citations (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AUPR043300A0 (en) * 2000-09-29 2000-10-19 Compco Pty Ltd Halogen-free polymeric compositions
CN102336953A (en) * 2011-08-16 2012-02-01 河北中联塑胶科技发展有限公司 Environmentally-friendly low-smoke halogen-free flame-retardant photovoltaic cable insulation and sheath and preparation method thereof
CN102942351A (en) * 2012-10-31 2013-02-27 安徽美露达新型建材有限公司 High-strength keelless La Nina mineral wool board
CN103289282A (en) * 2013-05-06 2013-09-11 安徽格林生态高分子材料技术有限公司 Cable sheath material containing modified poly-phenyl ether resin and preparation method thereof
CN103467832A (en) * 2013-06-03 2013-12-25 公安部四川消防研究所 Low temperature-resistant flexible crosslinkable halogen-free flame retardant cable material and preparation method thereof
CN104610704A (en) * 2015-01-28 2015-05-13 清远市普塞呋磷化学有限公司 Halogen-free flame retardant anhydride cured epoxy resin composition
JP2015168697A (en) * 2014-03-05 2015-09-28 日立金属株式会社 Non-halogen flame-retardant resin composition, and insulated wire and cable using the same
CN105566745A (en) * 2014-10-15 2016-05-11 西安艾菲尔德复合材料科技有限公司 High-heat-resistant halogen-free flame-retardant polypropylene composite material
CN106496757A (en) * 2016-11-07 2017-03-15 中广核三角洲(中山)高聚物有限公司 A kind of resistance to 150 DEG C are exempted from irradiation oil-resistant low-smoke halogen-free flame-retardant cable material of polyolefin and preparation method thereof
JP2017095608A (en) * 2015-11-25 2017-06-01 住友電気工業株式会社 Flame-retardant resin composition and flame-retardant cable
CN108447603A (en) * 2018-02-07 2018-08-24 合肥达户电线电缆科技有限公司 A kind of electric vehicle charging high temperature resistant flexible cable
CN108659375A (en) * 2018-04-17 2018-10-16 安徽伙伴电气有限公司 A kind of carrying tensile type wind energy power cable certainly
CN110387127A (en) * 2019-07-22 2019-10-29 苏州卫生职业技术学院 A kind of high-performance correction chew and preparation method thereof
CN111073068A (en) * 2019-12-25 2020-04-28 浙江世泰实业有限公司 Butadiene rubber dust cover and preparation method thereof

Patent Citations (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AUPR043300A0 (en) * 2000-09-29 2000-10-19 Compco Pty Ltd Halogen-free polymeric compositions
CN102336953A (en) * 2011-08-16 2012-02-01 河北中联塑胶科技发展有限公司 Environmentally-friendly low-smoke halogen-free flame-retardant photovoltaic cable insulation and sheath and preparation method thereof
CN102942351A (en) * 2012-10-31 2013-02-27 安徽美露达新型建材有限公司 High-strength keelless La Nina mineral wool board
CN103289282A (en) * 2013-05-06 2013-09-11 安徽格林生态高分子材料技术有限公司 Cable sheath material containing modified poly-phenyl ether resin and preparation method thereof
CN103467832A (en) * 2013-06-03 2013-12-25 公安部四川消防研究所 Low temperature-resistant flexible crosslinkable halogen-free flame retardant cable material and preparation method thereof
JP2015168697A (en) * 2014-03-05 2015-09-28 日立金属株式会社 Non-halogen flame-retardant resin composition, and insulated wire and cable using the same
CN105566745A (en) * 2014-10-15 2016-05-11 西安艾菲尔德复合材料科技有限公司 High-heat-resistant halogen-free flame-retardant polypropylene composite material
CN104610704A (en) * 2015-01-28 2015-05-13 清远市普塞呋磷化学有限公司 Halogen-free flame retardant anhydride cured epoxy resin composition
JP2017095608A (en) * 2015-11-25 2017-06-01 住友電気工業株式会社 Flame-retardant resin composition and flame-retardant cable
CN106496757A (en) * 2016-11-07 2017-03-15 中广核三角洲(中山)高聚物有限公司 A kind of resistance to 150 DEG C are exempted from irradiation oil-resistant low-smoke halogen-free flame-retardant cable material of polyolefin and preparation method thereof
CN108447603A (en) * 2018-02-07 2018-08-24 合肥达户电线电缆科技有限公司 A kind of electric vehicle charging high temperature resistant flexible cable
CN108659375A (en) * 2018-04-17 2018-10-16 安徽伙伴电气有限公司 A kind of carrying tensile type wind energy power cable certainly
CN110387127A (en) * 2019-07-22 2019-10-29 苏州卫生职业技术学院 A kind of high-performance correction chew and preparation method thereof
CN111073068A (en) * 2019-12-25 2020-04-28 浙江世泰实业有限公司 Butadiene rubber dust cover and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112641483A (en) * 2020-12-22 2021-04-13 江苏省中医药研究院 Automatic pressing hemostasis device after tooth extraction
CN116082785A (en) * 2023-04-10 2023-05-09 宏亮电缆有限公司 High-temperature-resistant mining cable of stranded copper conductor

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