CN111423673A - Heat-resistant and high-temperature-resistant PVC (polyvinyl chloride) power tube and preparation method thereof - Google Patents
Heat-resistant and high-temperature-resistant PVC (polyvinyl chloride) power tube and preparation method thereof Download PDFInfo
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- CN111423673A CN111423673A CN202010274740.XA CN202010274740A CN111423673A CN 111423673 A CN111423673 A CN 111423673A CN 202010274740 A CN202010274740 A CN 202010274740A CN 111423673 A CN111423673 A CN 111423673A
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- 229920000915 polyvinyl chloride Polymers 0.000 title claims abstract description 51
- 239000004800 polyvinyl chloride Substances 0.000 title claims abstract description 51
- 238000002360 preparation method Methods 0.000 title claims abstract description 22
- 239000002131 composite material Substances 0.000 claims abstract description 35
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical class O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 claims abstract description 32
- 239000000945 filler Substances 0.000 claims abstract description 30
- 239000004801 Chlorinated PVC Substances 0.000 claims abstract description 19
- 229920000457 chlorinated polyvinyl chloride Polymers 0.000 claims abstract description 19
- 239000006057 Non-nutritive feed additive Substances 0.000 claims abstract description 18
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 17
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 17
- 239000012760 heat stabilizer Substances 0.000 claims abstract description 16
- 239000004014 plasticizer Substances 0.000 claims abstract description 15
- 239000003365 glass fiber Substances 0.000 claims abstract description 11
- 230000002745 absorbent Effects 0.000 claims abstract description 10
- 239000002250 absorbent Substances 0.000 claims abstract description 10
- 239000002994 raw material Substances 0.000 claims abstract description 9
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000003063 flame retardant Substances 0.000 claims abstract description 8
- 239000000203 mixture Substances 0.000 claims description 31
- 238000006243 chemical reaction Methods 0.000 claims description 26
- 238000010438 heat treatment Methods 0.000 claims description 26
- 238000003756 stirring Methods 0.000 claims description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 25
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 18
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 18
- 229910052901 montmorillonite Inorganic materials 0.000 claims description 15
- 239000008367 deionised water Substances 0.000 claims description 14
- 229910021641 deionized water Inorganic materials 0.000 claims description 14
- ZBBLRPRYYSJUCZ-GRHBHMESSA-L (z)-but-2-enedioate;dibutyltin(2+) Chemical compound [O-]C(=O)\C=C/C([O-])=O.CCCC[Sn+2]CCCC ZBBLRPRYYSJUCZ-GRHBHMESSA-L 0.000 claims description 13
- 238000001816 cooling Methods 0.000 claims description 13
- 238000001035 drying Methods 0.000 claims description 13
- 238000001914 filtration Methods 0.000 claims description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
- 238000002156 mixing Methods 0.000 claims description 10
- 239000012065 filter cake Substances 0.000 claims description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims description 9
- 239000000178 monomer Substances 0.000 claims description 8
- MGWAVDBGNNKXQV-UHFFFAOYSA-N diisobutyl phthalate Chemical compound CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C MGWAVDBGNNKXQV-UHFFFAOYSA-N 0.000 claims description 6
- 239000011790 ferrous sulphate Substances 0.000 claims description 6
- 235000003891 ferrous sulphate Nutrition 0.000 claims description 6
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 claims description 6
- 229910000359 iron(II) sulfate Inorganic materials 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- 239000000725 suspension Substances 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 6
- YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 claims description 5
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 claims description 5
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 5
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 5
- 239000005062 Polybutadiene Substances 0.000 claims description 5
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims description 5
- -1 diester adipate Chemical class 0.000 claims description 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 5
- 229930195729 fatty acid Natural products 0.000 claims description 5
- 239000000194 fatty acid Substances 0.000 claims description 5
- 239000008103 glucose Substances 0.000 claims description 5
- 239000004816 latex Substances 0.000 claims description 5
- 229920000126 latex Polymers 0.000 claims description 5
- 239000012299 nitrogen atmosphere Substances 0.000 claims description 5
- 229920002857 polybutadiene Polymers 0.000 claims description 5
- 239000000344 soap Substances 0.000 claims description 5
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 claims description 5
- 229940048086 sodium pyrophosphate Drugs 0.000 claims description 5
- 235000019818 tetrasodium diphosphate Nutrition 0.000 claims description 5
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 claims description 5
- 239000006097 ultraviolet radiation absorber Substances 0.000 claims description 5
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 4
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 claims description 4
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 claims description 4
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 4
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 claims description 4
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 4
- 229910052700 potassium Inorganic materials 0.000 claims description 4
- 239000011591 potassium Substances 0.000 claims description 4
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims description 4
- IHBCFWWEZXPPLG-UHFFFAOYSA-N [Ca].[Zn] Chemical compound [Ca].[Zn] IHBCFWWEZXPPLG-UHFFFAOYSA-N 0.000 claims description 3
- 239000006084 composite stabilizer Substances 0.000 claims description 3
- 235000019441 ethanol Nutrition 0.000 claims description 3
- 125000005456 glyceride group Chemical group 0.000 claims description 3
- 238000000227 grinding Methods 0.000 claims description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 3
- 238000004321 preservation Methods 0.000 claims description 3
- 235000012424 soybean oil Nutrition 0.000 claims description 3
- 239000003549 soybean oil Substances 0.000 claims description 3
- 238000009210 therapy by ultrasound Methods 0.000 claims description 3
- 239000000835 fiber Substances 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 239000011159 matrix material Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 description 19
- 239000000243 solution Substances 0.000 description 12
- 239000011259 mixed solution Substances 0.000 description 7
- 238000007599 discharging Methods 0.000 description 6
- 238000005303 weighing Methods 0.000 description 6
- 230000002572 peristaltic effect Effects 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- NVJCKICOBXMJIJ-UHFFFAOYSA-M potassium;1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate Chemical compound [K+].C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C([O-])=O NVJCKICOBXMJIJ-UHFFFAOYSA-M 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000011152 fibreglass Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-LZFNBGRKSA-N Potassium-45 Chemical group [45K] ZLMJMSJWJFRBEC-LZFNBGRKSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-N hexanedioic acid Natural products OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- ZLMJMSJWJFRBEC-OUBTZVSYSA-N potassium-40 Chemical group [40K] ZLMJMSJWJFRBEC-OUBTZVSYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000004804 winding Methods 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
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/06—Homopolymers or copolymers of vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
-
- 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
- C08L2203/18—Applications used for pipes
-
- 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
-
- 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
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Abstract
The invention relates to the technical field of power pipes, in particular to a heat-resistant and high-temperature-resistant PVC power pipe and a preparation method thereof, and the heat-resistant and high-temperature-resistant PVC power pipe comprises the following raw materials in parts by weight: 90-110 parts of PVC, 95-105 parts of CPVC, 30-45 parts of composite modified filler, 2-3 parts of heat stabilizer, 40-60 parts of plasticizer, 1-2 parts of processing aid, 0.5-1.5 parts of flame retardant, 0.5-1 part of antioxidant and 0.5-1 part of ultraviolet absorbent, wherein the composite modified filler takes nano glass fiber as a framework, and an ABS/modified montmorillonite composite layer is coated outside the framework. The heat-resistant and high-temperature-resistant PVC electric power tube prepared by the invention is modified by adding the composite modified filler into the matrix material, and has good heat-resistant and high-temperature-resistant properties.
Description
Technical Field
The invention relates to the technical field of power tubes, in particular to a heat-resistant and high-temperature-resistant PVC power tube and a preparation method thereof.
Background
The development of electric power energy is related to national civilization and national safety, along with the continuous and rapid development of the economic society of China, the electric power demand also enters a high-speed growth period, recently, the development of urban planning and construction and the tidiness and beauty of urban appearance are realized, high-voltage electric wires are required to be completely buried underground, and because the high voltage of the high-voltage cable is high, the high temperature is easily generated by heating or is generated by instant accidental short circuit, people usually use plastic pipelines, metal pipelines or glass steel tubes as the protective pipe sleeve materials of the high-voltage cable.
The metal pipeline has poor corrosion resistance, and the service life is generally corroded and damaged only 15-30 years; the glass fiber reinforced plastic pipe is easy to pollute in production and use due to the adoption of a glass fiber winding coating process, is high in brittleness, cannot resist heavy pressure, beating or collision, is easy to delaminate, and influences service life, so that the plastic electric power pipe is gradually favored by people, and gradually replaces a metal pipeline and a glass fiber reinforced plastic pipe.
The PVC material has the characteristics of good rigidity, high strength, flame retardance, corrosion resistance and good electrical insulation; and the processing performance is good, the price is low, so the method has wide application in the electric power tube industry. The existing polyvinyl chloride electric power tube is made by using polyvinyl chloride resin as a base material, adding a plasticizer, a stabilizer and a processing aid, and processing the polyvinyl chloride by a special mixing device, but the polyvinyl chloride has poor stability to light and heat, the softening point is 80 ℃, the decomposition starts at 130 ℃, the polyvinyl chloride starts to decompose at 100 ℃ under the condition of not adding a heat stabilizer, and the decomposition is faster at more than 130 ℃, so that the improvement on the high temperature resistance of the polyvinyl chloride electric power tube is necessary.
Disclosure of Invention
In view of the above, the invention aims to provide a heat-resistant and high-temperature-resistant PVC power pipe and a preparation method thereof, and the prepared power pipe is modified by adding a composite modified filler into a base material, and has good heat-resistant and high-temperature-resistant properties, flame retardancy and the like.
The invention solves the technical problems by the following technical means:
a heat-resistant and high-temperature-resistant PVC electric power pipe comprises the following raw materials in parts by weight: 90-110 parts of PVC, 95-105 parts of CPVC, 30-45 parts of composite modified filler, 2-3 parts of heat stabilizer, 40-60 parts of plasticizer, 1-2 parts of processing aid, 0.5-1 part of antioxidant and 0.5-1 part of ultraviolet absorbent, wherein the composite modified filler takes nano glass fiber as a framework, and an ABS/modified montmorillonite composite layer is coated outside the framework.
The PVC power tube of the invention takes a PVC and CPVC composite substrate material as a substrate material, chlorinated polyvinyl chloride is a product obtained by further chlorinating PVC resin, and has better heat resistance and mechanical property compared with PVC resin, and the thermal deformation temperature of the polyvinyl chloride can be greatly improved by adding the chlorinated polyvinyl chloride into the polyvinyl chloride substrate material The network structure and the nanometer glass fiber provide the connection and support function for the three-dimensional structure, so that the three-dimensional network structure is more stable, and the heat resistance and the high temperature resistance of the power tube are further improved.
Further, the PVC electric power pipe comprises the following raw materials in parts by weight: 100 parts of PVC, 95 parts of CPVC, 40 parts of composite modified filler, 2 parts of heat stabilizer, 50 parts of plasticizer, 1 part of processing aid, 0.8 part of antioxidant and 0.6 part of ultraviolet absorber.
Further, the plasticizer is at least one of glyceride, epoxidized soybean oil, adipic acid diester and diisobutyl phthalate.
Further, the heat stabilizer is one or two of a calcium-zinc composite stabilizer and zinc stearate.
Further, the processing aid is ACR401, and the antioxidant is 1076.
In addition, the invention also discloses a preparation method of the heat-resistant high-temperature-resistant PVC electric power tube, which comprises the following steps:
PVC, CPVC, composite modified filler, a heat stabilizer, a plasticizer, a processing aid, an antioxidant, a flame retardant and an ultraviolet absorbent are respectively weighed according to the proportion, the PVC and the CPVC are firstly added into a high-speed mixer, the heat stabilizer is added after the mixture is subjected to hot mixing to 65 ℃, the plasticizer and the processing aid are added after the mixture is heated to 80 ℃, the composite modified filler, the antioxidant, the flame retardant and the ultraviolet absorbent are added after the mixture is heated to 90 ℃, the mixture is discharged to a cold mixer for cooling when the temperature of the mixture reaches 110-130 ℃, the mixture is discharged when the temperature of the mixture is reduced to 55 ℃ in the cold mixer, the mixture is conveyed to a double-screw extruder, and the electric power tube is obtained after the mixture is extruded.
Further, the technological parameters of the double-screw extruder are as follows: the first zone is: 195-plus-200 ℃, 185-plus-190 ℃ in the second zone, 180-plus-185 ℃ in the third zone, 175-plus-180 ℃ in the fourth zone, 165-plus-170 ℃ in the fifth zone, 180-190 ℃ in the head temperature, 10-30 ℃ in the water cooling temperature and 5-7m/min in the traction speed.
Further, the preparation of the composite modified filler is specifically that 50-75 parts by weight of deionized water, 10-20 parts by weight of α -methylstyrene, 3-6 parts by weight of acrylonitrile, 0.01-0.02 part by weight of tert-dodecyl mercaptan, 0.1-0.2 part by weight of cumene hydroperoxide and 1.2-1.5 parts by weight of rosin acid soap are stirred and mixed to obtain a monomer mixed solution, 100 parts by weight of deionized water, 0.18-0.3 part by weight of glucose, 0.12-0.15 part by weight of sodium pyrophosphate, 0.25-0.4 part by weight of fatty acid potassium salt and 0.00015-0.0003 part by weight of ferrous sulfate solution are added into a reaction kettle, the mixture is stirred until solids are completely dissolved, 1.8-3 parts by weight of potassium rosinate, 0.15-0.25 part by weight of potassium hydroxide and 30-45 parts by weight of polybutadiene latex are added, nitrogen is added, 2-3 parts by weight of modified montmorillonite is added under nitrogen, after stirring and dispersion, 8-10 parts by weight of nano glass fiber is added, peristaltic movement is carried out until the temperature rise to 60 hours, the reaction is finished, the temperature is raised, the mixture is dried, and the temperature is raised to 80 ℃, and the reaction kettle is heated and dried.
Further, the preparation method of the modified montmorillonite specifically comprises the following steps:
s1: stirring and dispersing montmorillonite in deionized water, ultrasonically dispersing for 30 minutes, adding p-phenylenediamine and ammonia water under the protection of nitrogen, stirring and reacting for 4 hours, then heating to 80 ℃, preserving heat and reacting for 4 hours, filtering, washing a filter cake with hot water and absolute ethyl alcohol, drying, and ultrasonically dispersing in toluene to obtain a suspension solution;
s2: dissolving di-n-butyltin maleate in toluene, heating to 120 ℃, performing ultrasonic treatment until the solution is completely dissolved, adding the suspension, heating to 100 ℃ in a nitrogen atmosphere, performing heat preservation reaction for 12 hours, slowly pouring the reaction solution into low-temperature ethanol after the reaction is finished, filtering, and drying the filter cake at 80 ℃ for 48 hours to obtain the di-n-butyltin maleate grafted montmorillonite;
s3: stirring and dispersing the di-n-butyltin maleate grafted montmorillonite in deionized water, adding hexadecyl trimethyl ammonium bromide, heating to 70 ℃, continuously stirring and reacting for 6 hours, filtering after the reaction is finished, and washing, drying and grinding a filter cake to obtain the modified montmorillonite.
The di-n-butyltin maleate is used as a heat stabilizer of the PVC material and is grafted to the surface of montmorillonite, firstly, the di-n-butyltin maleate can improve the heat stability of the body material and is grafted to the surface of the montmorillonite to play a role in fixing the montmorillonite, and the probability that the di-n-butyltin maleate moves from the inside of the base material to the surface is reduced to a certain extent in the using process, so that the probability of the phenomenon of frosting of the power pipe is reduced.
The invention has the beneficial effects that:
the power tube disclosed by the invention has the advantages that the PVC and the CPVC are compounded to be used as the base material of the power tube, compared with the traditional PVC power tube, the power tube has better heat resistance, the composite modified filler is added into the raw materials, the nano glass fiber is used as a framework, the ABS/modified montmorillonite composite layer is compounded and coated on the surface of the nano glass fiber, the thermal deformation temperature and the thermal stability of the power tube are improved through the mutual cooperation of the components, and meanwhile, the mechanical property of the power tube is also improved.
Detailed Description
The present invention will be described in detail with reference to specific examples below:
according to the heat-resistant and high-temperature-resistant PVC power pipe, the composite modified filler is added into the base material to modify the base material, so that the heat-resistant and high-temperature-resistant PVC power pipe has good heat-resistant and high-temperature-resistant properties, and is prepared specifically as follows:
example one
Preparation of modified montmorillonite
S1, stirring and dispersing montmorillonite in deionized water according to a solid-liquid ratio of 3 g/L, ultrasonically dispersing for 30 minutes, adding p-phenylenediamine and ammonia water under the condition of nitrogen protection, wherein the mass ratio of montmorillonite to p-phenylenediamine to ammonia water is 1:5:5, stirring and reacting for 4 hours, heating to 80 ℃, keeping the temperature and reacting for 4 hours, filtering, washing a filter cake with hot water and absolute ethyl alcohol, drying, and ultrasonically dispersing in toluene according to a solid-liquid ratio of 2 g/L to obtain a suspension solution;
s2: dissolving 10 times of montmorillonite mass of di-n-butyltin maleate in toluene, heating the solution to 120 ℃ and carrying out ultrasonic treatment until the solution is completely dissolved, adding the suspension, heating the solution to 100 ℃ in a nitrogen atmosphere, carrying out heat preservation reaction for 12 hours, slowly pouring the reaction solution into low-temperature ethanol after the reaction is finished, filtering, and drying the filter cake at 80 ℃ for 48 hours to obtain the di-n-butyltin maleate grafted montmorillonite;
s3: stirring and dispersing the di-n-butyltin maleate grafted montmorillonite in deionized water, adding hexadecyl trimethyl ammonium bromide, heating to 70 ℃, continuously stirring and reacting for 6 hours, filtering after the reaction is finished, washing a filter cake, drying in vacuum at 60 ℃, and grinding to obtain the modified montmorillonite, wherein the mass ratio of the di-n-butyltin maleate grafted montmorillonite to the deionized water to the hexadecyl trimethyl ammonium bromide is 1:20: 0.1.
Preparation of composite modified filler
Respectively weighing 30 parts by weight of deionized water, 15 parts by weight of α -methyl styrene, 5 parts of acrylonitrile, 0.01 part of tert-dodecyl mercaptan, 0.2 part of cumene hydroperoxide and 1.2 parts of abietic acid soap, stirring and mixing to obtain a monomer mixed solution, respectively adding 70 parts by weight of ionized water, 0.25 part by weight of glucose, 0.14 part by weight of sodium pyrophosphate, 0.3 part by weight of potassium fatty acid salt and 0.0002 part by weight of ferrous sulfate solution into a reaction kettle, stirring until the solids are completely dissolved, adding 2 parts by weight of potassium abietate, 0.2 part by weight of potassium hydroxide and 40 parts by weight of polybutadiene latex, introducing nitrogen, adding 2 parts by weight of modified montmorillonite under the nitrogen atmosphere, stirring and dispersing, adding 9 parts by weight of nano glass fiber, heating to 75 ℃, continuously adding the monomer mixed solution into the reaction kettle by a peristaltic pump for 5 hours, heating to 80 ℃, keeping the temperature for 1 hour, cooling to 60 ℃, stopping the reaction, filtering, dehydrating and drying to obtain the composite demulsification modified filler.
Preparation of electric power tube
Firstly, weighing the following components in proportion respectively: 90 parts of PVC, 105 parts of CPVC, 30 parts of composite modified filler, 2 parts of calcium-zinc composite stabilizer, 40 parts of glyceride, 4011 parts of processing aid ACR, 10760.5 parts of antioxidant and 0.5 part of UV531 ultraviolet absorber.
Adding PVC and CPVC into a high-speed mixer, hot mixing to 65 ℃, adding a heat stabilizer, heating to 80 ℃, adding a plasticizer and a processing aid, heating to 90 ℃, adding a composite modified filler, an antioxidant, a flame retardant and an ultraviolet absorbent, discharging materials to a cold mixer for cooling when the temperature of the mixture reaches 110-130 ℃, discharging materials when the temperature of the mixture in the cold mixer is reduced to 55 ℃, conveying the raw materials to a double-screw extruder, and setting the technological parameters of the double-screw extruder as follows: the first zone is 190 ℃, the second zone is 185 ℃, the third zone is 180 ℃, the fourth zone is 175 ℃, the fifth zone is 170 ℃, the head temperature is 180 ℃, the water cooling temperature is 10 ℃, the traction speed is 6m/min, and the electric power tube is obtained after being extruded by a double-screw extruder.
Example two
The preparation of the modified montmorillonite is the same as that of the first embodiment.
Preparation of composite modified filler
Respectively weighing 50 parts by weight of deionized water, 10 parts by weight of α -methyl styrene, 3 parts of acrylonitrile, 0.01 part of tert-dodecyl mercaptan, 0.1 part of cumene hydroperoxide and 1.4 parts by weight of abietic acid soap, stirring and mixing to obtain a monomer mixed solution, respectively adding 100 parts by weight of ionized water, 0.3 part of glucose, 0.15 part of sodium pyrophosphate, 0.4 part of fatty acid potassium salt and 0.0003 part of ferrous sulfate solution into a reaction kettle, stirring until the solids are completely dissolved, adding 3 parts by weight of potassium abietate, 0.25 part of potassium hydroxide and 45 parts by weight of polybutadiene latex, introducing nitrogen, adding 2 parts by weight of modified montmorillonite under the nitrogen atmosphere, stirring and dispersing, adding 8 parts by weight of nano glass fiber, heating to 75 ℃, continuously adding the monomer mixed solution into the reaction kettle by a peristaltic pump for 5 hours, heating to 80 ℃, keeping the temperature for 1 hour, cooling to 60 ℃, stopping the reaction, filtering, dehydrating and drying to obtain the composite demulsification modified filler.
Preparation of electric power tube
Firstly, weighing the following components in proportion respectively: 100 parts of PVC, 95 parts of CPVC, 40 parts of composite modified filler, 2 parts of zinc stearate, 50 parts of epoxidized soybean oil, 4011 parts of processing aid ACR, 10760.8 parts of antioxidant and 0.6 part of UV531 ultraviolet absorber.
Adding PVC and CPVC into a high-speed mixer, hot mixing to 65 ℃, adding a heat stabilizer, heating to 80 ℃, adding a plasticizer and a processing aid, heating to 90 ℃, adding a composite modified filler, an antioxidant, a flame retardant and an ultraviolet absorbent, discharging materials to a cold mixer for cooling when the temperature of the mixture reaches 110-130 ℃, discharging materials when the temperature of the mixture in the cold mixer is reduced to 55 ℃, conveying the raw materials to a double-screw extruder, and setting the technological parameters of the double-screw extruder as follows: the temperature of the first zone is 195 ℃, the temperature of the second zone is 185 ℃, the temperature of the third zone is 180 ℃, the temperature of the fourth zone is 175 ℃, the temperature of the fifth zone is 165 ℃, the temperature of a machine head is 180 ℃, the temperature of water cooling is 30 ℃, the traction speed is 5m/min, and the electric power tube is obtained after being extruded by a double-screw extruder.
EXAMPLE III
The preparation of the modified montmorillonite is the same as that of the first embodiment.
Preparation of composite modified filler
Respectively weighing 75 parts by weight of deionized water, 20 parts by weight of α -methylstyrene, 6 parts of acrylonitrile, 0.02 part by weight of tert-dodecyl mercaptan, 0.2 part by weight of cumene hydroperoxide and 1.5 parts by weight of abietic acid soap, stirring and mixing to obtain a monomer mixed solution, respectively adding 125 parts by weight of ionized water, 0.18 part by weight of glucose, 0.12 part by weight of sodium pyrophosphate, 0.25 part by weight of potassium fatty acid salt and 0.00015 part by weight of ferrous sulfate solution into a reaction kettle, stirring until the solids are completely dissolved, adding 1.8 parts by weight of potassium abietate, 0.15 part by weight of potassium hydroxide and 30 parts by weight of polybutadiene latex, introducing nitrogen, adding 3 parts by weight of modified montmorillonite under the atmosphere of nitrogen, stirring and dispersing, adding 10 parts by weight of nano glass fiber, heating to 75 ℃, continuously adding the monomer mixed solution into the reaction kettle by a peristaltic pump for 5 hours, after the reaction is completed, heating to 80 ℃, keeping the temperature for 1 hour, cooling to 60 ℃, stopping the reaction, filtering, dehydrating and demulsifying to obtain the composite modified filler.
Preparation of electric power tube
Firstly, weighing the following components in proportion respectively: 110 parts of PVC, 100 parts of CPVC, 45 parts of composite modified filler, 3 parts of zinc stearate, 60 parts of diisobutyl phthalate, 4012 parts of processing aid ACR, 10761 parts of antioxidant and 1 part of UV531 ultraviolet absorber.
Adding PVC and CPVC into a high-speed mixer, hot mixing to 65 ℃, adding a heat stabilizer, heating to 80 ℃, adding a plasticizer and a processing aid, heating to 90 ℃, adding a composite modified filler, an antioxidant, a flame retardant and an ultraviolet absorbent, discharging materials to a cold mixer for cooling when the temperature of the mixture reaches 110-130 ℃, discharging materials when the temperature of the mixture in the cold mixer is reduced to 55 ℃, conveying the raw materials to a double-screw extruder, and setting the technological parameters of the double-screw extruder as follows: the first zone is 200 ℃, the second zone is 190 ℃, the third zone is 185 ℃, the fourth zone is 180 ℃, the fifth zone is 170 ℃, the head temperature is 190 ℃, the water cooling temperature is 20 ℃, the traction speed is 7m/min, and the electric power tube is obtained after extrusion by a double-screw extruder.
Although the present invention has been described in detail with reference to the preferred embodiments, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted without departing from the spirit and scope of the invention as defined in the appended claims. The techniques, shapes, and configurations not described in detail in the present invention are all known techniques.
Claims (9)
1. The heat-resistant and high-temperature-resistant PVC electric power pipe is characterized by comprising the following raw materials in parts by weight: 90-110 parts of PVC, 95-105 parts of CPVC, 30-45 parts of composite modified filler, 2-3 parts of heat stabilizer, 40-60 parts of plasticizer, 1-2 parts of processing aid, 0.5-1 part of antioxidant and 0.5-1 part of ultraviolet absorbent, wherein the composite modified filler takes nano glass fiber as a framework, and an ABS/modified montmorillonite composite layer is coated outside the framework.
2. The heat-resistant high-temperature-resistant PVC electric power pipe as claimed in claim 1, which comprises the following raw materials in parts by weight: 100 parts of PVC, 95 parts of CPVC, 40 parts of composite modified filler, 2 parts of heat stabilizer, 50 parts of plasticizer, 1 part of processing aid, 0.8 part of antioxidant and 0.6 part of ultraviolet absorber.
3. A heat and temperature resistant PVC power pipe as claimed in claim 2, wherein said plasticizer is at least one of glyceride, epoxidized soybean oil, diester adipate, diisobutyl phthalate.
4. A heat and high temperature resistant PVC power pipe as claimed in claim 3, wherein said heat stabilizer is one or both of calcium zinc composite stabilizer and zinc stearate.
5. The heat and temperature resistant PVC power pipe as claimed in claim 4, wherein the processing aid is ACR401 and the antioxidant is 1076.
6. The preparation method of the heat-resistant high-temperature-resistant PVC electric power pipe as claimed in any one of claims 1 to 5, wherein the preparation method specifically comprises the following steps:
PVC, CPVC, composite modified filler, a heat stabilizer, a plasticizer, a processing aid, an antioxidant, a flame retardant and an ultraviolet absorbent are respectively weighed according to the proportion, the PVC and the CPVC are firstly added into a high-speed mixer, the heat stabilizer is added after the mixture is subjected to hot mixing to 65 ℃, the plasticizer and the processing aid are added after the mixture is heated to 80 ℃, the composite modified filler, the antioxidant, the flame retardant and the ultraviolet absorbent are added after the mixture is heated to 90 ℃, the mixture is discharged to a cold mixer for cooling when the temperature of the mixture reaches 110-130 ℃, the mixture is discharged when the temperature of the mixture is reduced to 55 ℃ in the cold mixer, the mixture is conveyed to a double-screw extruder, and the electric power tube is obtained after the mixture is extruded.
7. The preparation method of the heat-resistant high-temperature-resistant PVC electric power pipe as claimed in claim 6, wherein the process parameters of the twin-screw extruder are as follows: the first zone is 195-plus-200 ℃, the second zone is 185-plus-190 ℃, the third zone is 180-plus-185 ℃, the fourth zone is 175-plus-180 ℃, the fifth zone is 165-plus-170 ℃, the head temperature is 180-190 ℃, the water cooling temperature is 10-30 ℃, and the traction speed is 5-7 m/min.
8. The method for preparing a heat-resistant and high-temperature-resistant PVC electric power tube as claimed in claim 7, wherein the composite modified filler is prepared by stirring and mixing 50-75 parts by weight of deionized water, 10-20 parts by weight of α -methylstyrene, 3-6 parts by weight of acrylonitrile, 0.01-0.02 part by weight of t-dodecyl mercaptan, 0.1-0.2 part by weight of cumene hydroperoxide and 1.2-1.5 parts by weight of abietic acid soap to obtain a monomer mixture, adding 100 parts by weight of deionized water, 0.18-0.3 part by weight of glucose, 0.12-0.15 part by weight of sodium pyrophosphate, 0.25-0.4 part by weight of potassium fatty acid salt and 0.00015-0.0003 part by weight of ferrous sulfate solution into a reaction kettle, stirring until the solids are completely dissolved, adding 1.8-3 parts by weight of potassium hydroxide, 0.15-0.25 part by weight of potassium hydroxide and 30-45 parts by weight of latex, adding 2-3 parts by weight of demulsifying-3 parts by weight of ferrous sulfate solution, stirring until the solids are completely dissolved, adding the modified montmorillonite, stirring, heating and drying the mixture to obtain a reaction mixture, adding the modified polybutadiene fiber, filtering, drying the mixture, and reacting the mixture at a temperature of the mixture after the temperature is increased to 75 ℃ and the temperature is increased to 80 ℃ is increased.
9. The preparation method of the heat-resistant high-temperature-resistant PVC electric power tube according to claim 8, wherein the preparation method of the modified montmorillonite specifically comprises the following steps:
s1: stirring and dispersing montmorillonite in deionized water, ultrasonically dispersing for 30 minutes, adding p-phenylenediamine and ammonia water under the protection of nitrogen, stirring and reacting for 4 hours, then heating to 80 ℃, preserving heat and reacting for 4 hours, filtering, washing a filter cake with hot water and absolute ethyl alcohol, drying, and ultrasonically dispersing in toluene to obtain a suspension solution;
s2: dissolving di-n-butyltin maleate in toluene, heating to 120 ℃, performing ultrasonic treatment until the solution is completely dissolved, adding the suspension, heating to 100 ℃ in a nitrogen atmosphere, performing heat preservation reaction for 12 hours, slowly pouring the reaction solution into low-temperature ethanol after the reaction is finished, filtering, and drying the filter cake at 80 ℃ for 48 hours to obtain the di-n-butyltin maleate grafted montmorillonite;
s3: stirring and dispersing the di-n-butyltin maleate grafted montmorillonite in deionized water, adding hexadecyl trimethyl ammonium bromide, heating to 70 ℃, continuously stirring and reacting for 6 hours, filtering after the reaction is finished, and washing, drying and grinding a filter cake to obtain the modified montmorillonite.
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CN115678179A (en) * | 2022-10-24 | 2023-02-03 | 北方中意新材料(桐庐)有限公司 | High-insulation modified polyvinyl chloride power tube and preparation method thereof |
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