CN117430786A - High-strength TPU material for charging pile cable and preparation method thereof - Google Patents
High-strength TPU material for charging pile cable and preparation method thereof Download PDFInfo
- Publication number
- CN117430786A CN117430786A CN202311777673.3A CN202311777673A CN117430786A CN 117430786 A CN117430786 A CN 117430786A CN 202311777673 A CN202311777673 A CN 202311777673A CN 117430786 A CN117430786 A CN 117430786A
- Authority
- CN
- China
- Prior art keywords
- charging pile
- tpu material
- pile cable
- double
- flame retardant
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000000463 material Substances 0.000 title claims abstract description 60
- 238000002360 preparation method Methods 0.000 title abstract description 14
- 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 31
- 239000003063 flame retardant Substances 0.000 claims abstract description 31
- 239000000843 powder Substances 0.000 claims abstract description 25
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 24
- 229920005862 polyol Polymers 0.000 claims abstract description 23
- 150000003077 polyols Chemical class 0.000 claims abstract description 23
- 239000004970 Chain extender Substances 0.000 claims abstract description 21
- 239000012948 isocyanate Substances 0.000 claims abstract description 21
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 21
- 239000004205 dimethyl polysiloxane Substances 0.000 claims abstract description 19
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims abstract description 19
- 230000002195 synergetic effect Effects 0.000 claims abstract description 19
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 16
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 16
- 239000003054 catalyst Substances 0.000 claims abstract description 16
- 239000006097 ultraviolet radiation absorber Substances 0.000 claims abstract description 15
- 239000002270 dispersing agent Substances 0.000 claims abstract description 14
- 230000007062 hydrolysis Effects 0.000 claims abstract description 14
- 238000006460 hydrolysis reaction Methods 0.000 claims abstract description 14
- 239000002131 composite material Substances 0.000 claims abstract description 13
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims abstract description 12
- -1 polydimethylsiloxane Polymers 0.000 claims abstract description 12
- 239000002994 raw material Substances 0.000 claims abstract description 10
- 150000002009 diols Chemical class 0.000 claims abstract description 7
- 229920001610 polycaprolactone Polymers 0.000 claims abstract description 7
- 229920000909 polytetrahydrofuran Polymers 0.000 claims abstract description 7
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000004632 polycaprolactone Substances 0.000 claims abstract description 6
- 150000001875 compounds Chemical group 0.000 claims abstract description 4
- 238000013329 compounding Methods 0.000 claims abstract 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- DCXXMTOCNZCJGO-UHFFFAOYSA-N tristearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 claims description 10
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 claims description 9
- 238000006116 polymerization reaction Methods 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- 239000002250 absorbent Substances 0.000 claims description 6
- 230000002745 absorbent Effects 0.000 claims description 6
- 150000001718 carbodiimides Chemical group 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 238000005520 cutting process Methods 0.000 claims description 5
- QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 claims description 5
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 claims description 4
- 229940075507 glyceryl monostearate Drugs 0.000 claims description 4
- 238000005469 granulation Methods 0.000 claims description 4
- 230000003179 granulation Effects 0.000 claims description 4
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 claims description 3
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N salicylic acid phenyl ester Natural products OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 claims description 3
- ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 claims description 2
- KXBFLNPZHXDQLV-UHFFFAOYSA-N [cyclohexyl(diisocyanato)methyl]cyclohexane Chemical compound C1CCCCC1C(N=C=O)(N=C=O)C1CCCCC1 KXBFLNPZHXDQLV-UHFFFAOYSA-N 0.000 claims description 2
- AGXUVMPSUKZYDT-UHFFFAOYSA-L barium(2+);octadecanoate Chemical compound [Ba+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AGXUVMPSUKZYDT-UHFFFAOYSA-L 0.000 claims description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims description 2
- 235000013539 calcium stearate Nutrition 0.000 claims description 2
- 239000008116 calcium stearate Substances 0.000 claims description 2
- LTGPEBRDBMFYBR-UHFFFAOYSA-N ethyl 4-[(n-ethylanilino)methylideneamino]benzoate Chemical compound C1=CC(C(=O)OCC)=CC=C1N=CN(CC)C1=CC=CC=C1 LTGPEBRDBMFYBR-UHFFFAOYSA-N 0.000 claims description 2
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical group OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 2
- 229920002635 polyurethane Polymers 0.000 abstract description 12
- 239000004814 polyurethane Substances 0.000 abstract description 12
- 230000000694 effects Effects 0.000 abstract description 5
- 238000002156 mixing Methods 0.000 abstract description 5
- 239000003112 inhibitor Substances 0.000 abstract description 4
- 239000011159 matrix material Substances 0.000 abstract description 3
- 239000004433 Thermoplastic polyurethane Substances 0.000 description 34
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 34
- 230000000052 comparative effect Effects 0.000 description 20
- 238000012360 testing method Methods 0.000 description 10
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 8
- 238000001556 precipitation Methods 0.000 description 7
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 5
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000000498 ball milling Methods 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 239000000806 elastomer Substances 0.000 description 4
- 239000004800 polyvinyl chloride Substances 0.000 description 4
- 238000002834 transmittance Methods 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 230000000051 modifying effect Effects 0.000 description 2
- 238000001291 vacuum drying Methods 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000013013 elastic material Substances 0.000 description 1
- 239000013536 elastomeric material Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
- DXZMANYCMVCPIM-UHFFFAOYSA-L zinc;diethylphosphinate Chemical compound [Zn+2].CCP([O-])(=O)CC.CCP([O-])(=O)CC DXZMANYCMVCPIM-UHFFFAOYSA-L 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
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- C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
- C08G18/7664—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
- C08G18/7671—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups containing only one alkylene bisphenyl group
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B9/00—Making granules
- B29B9/02—Making granules by dividing preformed material
- B29B9/06—Making granules by dividing preformed material in the form of filamentary material, e.g. combined with extrusion
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/92—Measuring, controlling or regulating
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3203—Polyhydroxy compounds
- C08G18/3206—Polyhydroxy compounds aliphatic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4266—Polycondensates having carboxylic or carbonic ester groups in the main chain prepared from hydroxycarboxylic acids and/or lactones
- C08G18/4269—Lactones
- C08G18/4277—Caprolactone and/or substituted caprolactone
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4854—Polyethers containing oxyalkylene groups having four carbon atoms in the alkylene group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/61—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6666—Compounds of group C08G18/48 or C08G18/52
- C08G18/667—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/6674—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
- C08G18/6677—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203 having at least three hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
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- C08G18/721—Two or more polyisocyanates not provided for in one single group C08G18/73 - C08G18/80
- C08G18/724—Combination of aromatic polyisocyanates with (cyclo)aliphatic polyisocyanates
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
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- C08G18/758—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing two or more cycloaliphatic rings
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K3/2279—Oxides; Hydroxides of metals of antimony
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
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- C08K9/06—Ingredients treated with organic substances with silicon-containing compounds
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92504—Controlled parameter
- B29C2948/92704—Temperature
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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)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
The invention relates to the technical field of polyurethane, in particular to a high-strength TPU material for a charging pile cable and a preparation method thereof. The raw materials of the high-strength TPU material for the charging pile cable comprise: mixing polyol, isocyanate, a composite chain extender, an antioxidant, a hydrolysis inhibitor, a catalyst, a dispersing agent, a synergistic flame retardant and an ultraviolet absorber; the mixed polyol is at least one of polycaprolactone diol and polytetramethylene ether glycol and is mixed with terminal-hydroxybutyl-terminated polydimethylsiloxane; the compound chain extender is prepared by compounding 1, 4-butanediol and trimethylolpropane; the synergistic flame retardant is silane coupling agent modified nano Sb 2 O 3 And (3) powder. The invention solves the problem of poor compatibility between the flame retardant and the matrix, and improves the flame retardant effect, heat resistance and mechanical property of the TPU material.
Description
Technical Field
The invention relates to the technical field of polyurethane, in particular to a high-strength TPU material for a charging pile cable and a preparation method thereof.
Background
Compared with the traditional cable material, the charging pile cable is an important supporting facility of a new energy automobile, and has higher requirements on the use environment and safety, so that higher requirements are also put forward on the coating material of the charging pile cable.
At present, two main materials are used for coating the charging pile cable: one is an elastomeric material based on polyvinyl chloride (PVC), such as: the PVC elastomer material for the electric automobile charging pile disclosed in the patent CN104194220A has better performance, can basically meet the use requirement of a charging pile cable and has lower price; however, the PVC elastomer has large smoke generation amount during combustion, does not accord with the trend of environmental protection, and greatly limits the use of PVC-based elastomer materials.
The other is an elastic material which takes thermoplastic polyurethane elastomer (TPU) as a base material, and the material is easy to process, has wide hardness range and excellent performance, and meets the requirement of environmental protection; however, TPU itself belongs to inflammable materials, and in order to achieve a sufficient flame retardant effect, a large amount of halogen-free flame retardant is required to be added, which can inhibit combustion or slow down flame propagation speed, but the addition of a large amount can have great influence on mechanical properties of the materials, and compatibility between filler and polymer is generally poor, and liquid flame retardant is easy to separate out. In addition, the heat resistance and mechanical properties of the TPU material also need to be further improved.
Disclosure of Invention
The invention aims to provide a high-strength TPU material for a charging pile cable, which is characterized in that flame retardant groups are grafted onto polyurethane molecular chains through reaction, so that the problem of poor compatibility between a flame retardant and a matrix is fundamentally solved, the flame retardant effect of the TPU material is improved, and the heat resistance and mechanical property of the TPU material are improved through the addition of end-hydroxybutyl-terminated polydimethylsiloxane, the crosslinking reaction and a two-section screw connection extrusion process; the invention also provides a preparation method of the composite.
The high-strength TPU material for the charging pile cable comprises the following raw materials in parts by mass:
50-70 parts of mixed polyol,
25-40 parts of isocyanate and the like,
5-10 parts of composite chain extender,
0.1 to 0.3 part of antioxidant,
0.05 to 0.2 part of hydrolysis resistant agent,
0.02-0.1 part of catalyst,
0.01 to 0.03 part of dispersing agent,
0.005-0.01 part of synergistic flame retardant,
0.05-0.3 part of ultraviolet absorber;
the mixed polyol is at least one of polycaprolactone diol (PCL) and polytetramethylene ether glycol (PTMG) and is mixed with terminal hydroxybutyl-terminated Polydimethylsiloxane (PDMS);
the compound chain extender is a compound of 85-99wt.% 1, 4-Butanediol (BDO) and 1-15wt.% Trimethylolpropane (TMP);
the isocyanate is a mixture of 90-95wt.% diphenylmethane diisocyanate (MDI) and 5-10wt.% dicyclohexylmethane diisocyanate (HMDI);
the synergistic flame retardant is silane coupling agent modified nano Sb 2 O 3 And (3) powder.
Preferably, the number average molecular weight of the polycaprolactone diol and the polytetramethylene ether glycol is 500 to 2000.
Preferably, the number average molecular weight of the end-hydroxybutyl-terminated polydimethylsiloxane is 1500-2000, and the structural formula is as follows:
。
preferably, in the mixed polyol, the mass percentage of the end-hydroxybutyl-terminated polydimethylsiloxane is 5-15%.
Preferably, the silane coupling agent modifies nano Sb 2 O 3 Nano Sb in powder 2 O 3 The average particle diameter of the powder is between 30 and 50 nm.
The purpose of the silane coupling agent modification is to improve nano Sb 2 O 3 Dispersibility and compatibility of the powder. The silane coupling agent can be commercially available silane coupling agents, such as silane coupling agent KH-550, silane coupling agent KH-560 and the like, and the modification of the types has no obvious influence on the modification effect; the usage amount of the silane coupling agent is nanometer Sb 2 O 3 The powder quality is 0.05-0.2%, and the better modifying effect can be achieved in the dosage range.
In one embodiment, the silane coupling agent modifies nano Sb 2 O 3 The preparation method of the powder comprises the following steps:
nano Sb with average particle diameter of 30-50nm 2 O 3 The powder, the silane coupling agent KH-550 and absolute ethyl alcohol are jointly placed in a ball milling tank according to the mass ratio of 1:0.05:2, ball milling is carried out for 10 hours under the condition of rotating speed of 500r/min, and then vacuum drying is carried out, thus obtaining the silane coupling agent modified nano Sb 2 O 3 And (3) powder.
Preferably, the antioxidant is phosphite antioxidant; further preferred is tris (2, 4-di-tert-butylphenyl) phosphite.
Preferably, the hydrolysis resistance agent is carbodiimide.
Preferably, the catalyst is an organotin catalyst; stannous octoate is further preferred.
Preferably, the dispersing agent is at least one of glyceryl monostearate, glyceryl tristearate, barium stearate and calcium stearate; further preferred is a mixture of glyceryl monostearate and glyceryl tristearate in a mass ratio of 1:1.5.
Preferably, the ultraviolet absorber is at least one of N- (ethoxycarbonylphenyl) -N '-methyl-N' -phenylamidine (UV-1), N- (ethoxycarbonylphenyl) -N '-ethyl-N' -phenylformamidine (UV-2), phenyl O-hydroxybenzoate, 2- (2 '-hydroxy-5' -methylphenyl) benzotriazole (UV-P), 2, 4-dihydroxybenzophenone (UV-O), 2-hydroxy-4-methoxybenzophenone (UV-9), 2-hydroxy-4-N-octoxybenzophenone (UV-531); further preferred is N- (ethoxycarbonylphenyl) -N '-methyl-N' -phenylamidine (UV-1).
The preparation method of the high-strength TPU material for the charging pile cable comprises the following steps:
adopting a two-section double-screw extruder connected with a middle double-shaft double-screw and a long double-shaft double-screw to carry out continuous polymerization reaction, firstly adding an antioxidant, a hydrolysis-resistant agent, a dispersing agent, a synergistic flame retardant and an ultraviolet absorbent into mixed polyol, and carrying out prepolymerization reaction with partial isocyanate and a catalyst in the middle double-shaft double-screw to obtain a prepolymer; and then conveying the prepolymer into a long double-shaft double-screw rod, carrying out polymerization reaction with the residual isocyanate and the composite chain extender, and carrying out underwater cutting granulation to obtain the high-strength TPU material for the charging pile cable.
Preferably, the medium double-shaft double-screw is divided into four temperature zones, and the temperatures from the first zone to the fourth zone are 180 ℃, 185 ℃ and 190 ℃ in sequence; the rotating speed of the host machine is 180r/min.
Preferably, the long biaxial twin screw is divided into fourteen temperature zones, and the temperatures from the first zone to the fourteenth zone are 190 ℃, 195 ℃, 200 ℃, 205 ℃, 200 ℃, 195 ℃, 185 ℃, 180 ℃, 165, 180 ℃, 190 ℃ in sequence; the die outlet temperature was 215 ℃; the rotation speed of the host machine is 210r/min.
In one embodiment, the preparation method of the high-strength TPU material for the charging pile cable specifically comprises the following steps:
(1) Adding an antioxidant, a hydrolysis inhibitor, a dispersing agent, a synergistic flame retardant and an ultraviolet absorbent into mixed polyol, mixing by a stirring head, pouring the mixture into a first area of a middle double-shaft double-screw rod by a mixer, continuously pouring and pouring a catalyst into the mixer of the middle double-shaft double-screw rod by another piece of equipment, pouring 1/2 amount of isocyanate into the first area of the middle double-shaft double-screw rod, and carrying out prepolymerization reaction in the middle double-shaft double-screw rod to obtain a prepolymer; the temperature of the middle double-shaft double-screw is 180 ℃, 185 ℃ and 190 ℃ from the first zone to the fourth zone in sequence, and the rotating speed of the main machine is 180r/min;
(2) The prepolymer is conveyed to a first area of a long double-shaft double-screw main machine barrel through a medium double-shaft double-screw, a chain extender is poured into the first area of the long double-shaft double-screw main machine barrel, the rest 1/2 amount of isocyanate is poured into a second area of the long double-shaft double-screw main machine barrel, polymerization reaction is carried out in the long double-shaft double-screw, and the high-strength TPU material for the charging pile cable is obtained through underwater cutting, granulating and drying; the temperature of each zone is controlled by heating, and the temperatures from the first zone to the fourteenth zone are 190 ℃, 195 ℃, 200 ℃, 205 ℃, 200 ℃, 195 ℃, 185 ℃, 180 ℃, 165 ℃, 180 ℃, 190 ℃, the die outlet temperature is 215 ℃ and the host rotating speed is 210r/min.
Compared with the prior art, the invention has the following beneficial effects:
(1) The invention adopts at least one of polycaprolactone diol and polytetramethylene ether glycol and terminal hydroxybutyl-terminated polydimethylsiloxane to be mixed as a soft segment to synthesize silicon-containing block TPU, so as to promote microphase separation of polyurethane and improve the water resistance and mechanical property of polyurethane materials;
(2) The invention modifies nano Sb by adding silane coupling agent 2 O 3 The powder is used as a synergistic flame retardant, so that the flame retardance of the polyurethane material is effectively improved, and the silane coupling agent is used for modifying the nano Sb 2 O 3 The powder and polyurethane can be grafted to polyurethane molecular chains through reaction, so that the problem of poor compatibility between the flame retardant and the matrix is fundamentally solved, and meanwhile, the heat resistance and flame retardant effect of the polyurethane material are improved;
(3) According to the invention, the small molecular diol and the trimethylolpropane are mixed to serve as a chain extender, and the mechanical properties of the polyurethane material are further improved through a crosslinking reaction;
(4) The invention adopts a small amount of HMDI and MDI to mix, and can improve the transparency and yellowing resistance of the TPU material on the basis of ensuring the mechanical property of the TPU material;
(5) The invention adopts the production process of connecting the medium double-shaft double screw and the long double-shaft double screw, carries through the prepolymerization reaction of the medium double-shaft double screw, carries through the mixing polymerization reaction of the long double-shaft double screw, and carries out continuous production, thereby greatly improving the stability and the processing performance of the material, having high production efficiency, safety and environmental protection, and simultaneously, the two-section screw extrusion process ensures that the molecular chain segments of polyurethane are distributed more uniformly, the molecular chain of the obtained polyurethane is longer, and the mechanical property of the material is improved.
Detailed Description
The invention is further illustrated below with reference to examples.
The raw materials used in the examples, unless otherwise specified, were all commercially available conventional raw materials; the process used in the examples, unless otherwise specified, is conventional in the art.
Silane coupling agent modified nano Sb used in examples 2 O 3 The preparation method of the powder comprises the following steps:
nano Sb with average particle diameter of 30-50nm 2 O 3 The powder, the silane coupling agent KH-550 and absolute ethyl alcohol are jointly placed in a ball milling tank according to the mass ratio of 1:0.05:2, ball milling is carried out for 10 hours under the condition of rotating speed of 500r/min, and then vacuum drying is carried out, thus obtaining the silane coupling agent modified nano Sb 2 O 3 And (3) powder.
PTMG-1500 and PTMG-2000 adopted in the examples have number average molecular weights of 1500 and 2000 in sequence and are produced by Xiaoxing chemical industry (Jiaxing) Co., ltd;
the PCL-1500 and PCL-500 adopted in the examples have number average molecular weights of 1500 and 500 in sequence and are produced by Hunan kernel new material Co., ltd;
the PDMS used in the examples has a number average molecular weight of 1500-2000 and the structural formula is as follows:
。
example 1
The high-strength TPU material for the charging pile cable comprises the following raw materials in parts by mass:
60 parts of polyol (PTMG-1500 and PDMS in a mass ratio of 90:10) are mixed,
30 parts of isocyanate (mass ratio of 95:5 MDI and HMDI),
10 parts of composite chain extender (BDO and TMP with the mass ratio of 96:4),
0.2 part of antioxidant (tri (2, 4-di-tert-butylphenyl) phosphite),
0.15 part of hydrolysis resistance agent (carbodiimide),
0.07 part of catalyst (stannous octoate),
0.02 part of dispersing agent (glyceryl monostearate and glyceryl tristearate with the mass ratio of 1:1.5),
synergistic flame retardant (silane coupling agent modified nano Sb) 2 O 3 Powder) 0.01 part of the powder,
0.15 part of ultraviolet absorber (UV-1).
The preparation method comprises the following steps:
(1) Adding an antioxidant, a hydrolysis inhibitor, a dispersing agent, a synergistic flame retardant and an ultraviolet absorbent into mixed polyol, mixing by a stirring head, pouring the mixture into a first area of a middle double-shaft double-screw rod by a mixer, continuously pouring and pouring a catalyst into the mixer of the middle double-shaft double-screw rod by another piece of equipment, pouring 1/2 amount of isocyanate into the first area of the middle double-shaft double-screw rod, and carrying out prepolymerization reaction in the middle double-shaft double-screw rod to obtain a prepolymer; the temperature of the middle double-shaft double-screw is 180 ℃, 185 ℃ and 190 ℃ from the first zone to the fourth zone in sequence, and the rotating speed of the main machine is 180r/min;
(2) The prepolymer is conveyed to a first area of a long double-shaft double-screw main machine barrel through a medium double-shaft double-screw, the composite chain extender is poured into the first area of the long double-shaft double-screw main machine barrel, the rest 1/2 amount of isocyanate is poured into a second area of the long double-shaft double-screw main machine barrel, polymerization reaction is carried out in the long double-shaft double-screw, and the high-strength TPU material for the charging pile cable is obtained through underwater cutting granulation and drying; the temperature of each zone is controlled by heating, and the temperatures from the first zone to the fourteenth zone are 190 ℃, 195 ℃, 200 ℃, 205 ℃, 200 ℃, 195 ℃, 185 ℃, 180 ℃, 165 ℃, 180 ℃, 190 ℃, the die outlet temperature is 215 ℃ and the host rotating speed is 210r/min.
Example 2
This example differs from example 1 only in that the mass ratio of PTMG-1500 to PDMS in the mixed polyol is 95:5.
Example 3
This example differs from example 1 only in that the mass ratio of PTMG-1500 to PDMS in the mixed polyol is 85:15.
Example 4
The high-strength TPU material for the charging pile cable comprises the following raw materials in parts by mass:
70 parts of mixed polyol (PCL-500, PTMG-2000 and PDMS with the mass ratio of 45:45:10),
25 parts of isocyanate (mass ratio 92:8 MDI and HMDI),
5 parts of composite chain extender (BDO and TMP with the mass ratio of 90:10),
0.3 part of antioxidant (tri (2, 4-di-tert-butylphenyl) phosphite),
0.1 part of hydrolysis resistance agent (carbodiimide),
0.05 part of catalyst (stannous octoate),
0.03 part of dispersing agent (glyceryl tristearate),
synergistic flame retardant (silane coupling agent modified nano Sb) 2 O 3 Powder) 0.005 part of the total amount of the components,
0.1 part of ultraviolet absorber (UV-P).
The preparation method is the same as in example 1.
Example 5
The high-strength TPU material for the charging pile cable comprises the following raw materials in parts by mass:
65 parts of mixed polyol (PCL-1500 and PDMS in a mass ratio of 90:10),
28 parts of isocyanate (mass ratio of 95:5 MDI and HMDI),
7 parts of composite chain extender (BDO and TMP with the mass ratio of 99:1),
0.2 part of antioxidant (tri (2, 4-di-tert-butylphenyl) phosphite),
0.2 part of hydrolysis resistance agent (carbodiimide),
0.1 part of catalyst (stannous octoate),
0.01 part of dispersing agent (magnesium stearate),
synergistic flame retardant (silane coupling agent modified nano Sb) 2 O 3 Powder) 0.01 part of the powder,
0.3 parts of ultraviolet absorber (UV-O).
The preparation method is the same as in example 1.
Example 6
The high-strength TPU material for the charging pile cable comprises the following raw materials in parts by mass:
50 parts of a polyol (PCL-1500 and PDMS in a mass ratio of 90:10) are mixed,
40 parts of isocyanate (MDI and HMDI in a mass ratio of 90:10),
10 parts of composite chain extender (BDO and TMP with the mass ratio of 85:15),
0.1 part of antioxidant (tri (2, 4-di-tert-butylphenyl) phosphite),
0.05 part of hydrolysis resistance agent (carbodiimide),
0.02 part of catalyst (stannous octoate),
0.03 part of dispersing agent (stearic acid monoglyceride),
synergistic flame retardant (silane coupling agent modified nano Sb) 2 O 3 Powder) 0.01 part of the powder,
0.05 part of ultraviolet absorber (UV-2).
The preparation method is the same as in example 1.
Comparative example 1
This comparative example differs from example 1 only in that the mixed polyol was replaced with equal parts by weight of PTMG-1500.
Comparative example 2
Comparative example and example 1 do notThe same point is that no synergistic flame retardant is added (silane coupling agent modified nano Sb 2 O 3 Powder).
Comparative example 3
The only difference between this comparative example and example 1 is that the mass ratio of BDO and TMP in the complex chain extender is 80:20.
Comparative example 4
This comparative example differs from example 1 only in that the composite chain extender is replaced with equal parts by mass of BDO.
Comparative example 5
This comparative example differs from example 1 only in that the isocyanate used MDI and HMDI in a mass ratio of 80:20.
Comparative example 6
The comparative example uses the same raw material composition as example 1, except that the preparation method only uses a long biaxial twin screw, specifically as follows:
adding an antioxidant, a hydrolysis inhibitor, a dispersing agent, a synergistic flame retardant and an ultraviolet absorbent into mixed polyol, mixing the mixed polyol by a stirring head, pouring the mixed polyol into a first area of a long double-shaft double-screw main machine barrel by a mixer, pouring a composite chain extender into the first area of the long double-shaft double-screw main machine barrel, continuously pouring a catalyst into the mixer of the long double-shaft double-screw by another device, pouring isocyanate into the first area of the long double-shaft double-screw main machine barrel, performing polymerization reaction in the long double-shaft double-screw, and performing underwater cutting granulation and drying to obtain the high-strength TPU material for the charging pile cable.
The TPU materials prepared in the examples and comparative examples were subjected to performance tests in which:
tensile strength, elongation at break, 100% tensile stress were tested with reference to standard ASTM-D412;
tear strength is tested against standard ASTM-D624;
the light transmittance testing method comprises the following steps: injecting TPU material into a test piece with the thickness of 2mm, and testing the light transmittance of the test piece by adopting a color spectrum spectrocolorimeter CS-820;
the flame retardant level is tested according to the UL94 vertical burning test method, and the flame retardant level is V-0, V-1 and V-2 from high to low in sequence;
the conditions for testing the precipitation condition are as follows: placing the sample at 60 ℃ for 120 hours, taking out, standing for 3 hours at room temperature, observing and recording the precipitation condition of the surface of the sample, and dividing the sample into three grades of no precipitation, slight precipitation and obvious precipitation according to the precipitation amount;
the high temperature aging resistance test conditions are as follows: placing the sample at 100 ℃ for 168 hours, taking out, standing for 2 hours at room temperature, and testing the tensile strength and the elongation at break;
the water resistance test conditions were: the test piece was placed in 80 ℃ water for 168 hours, taken out and left at room temperature for 1 hour, and the tensile strength and elongation at break were tested.
The test results are shown in Table 1.
TABLE 1
As can be seen from Table 1, examples 1 to 6 of the present invention use PDMS to synthesize the block TPU, and the TPU material prepared by the continuous production process of reaction flame retardance and synergistic flame retardance, chain extender crosslinking, medium double-shaft double-screw and long double-shaft double-screw connection has high flame retardance, good mechanical property, high transparency, good heat resistance and water resistance, and no precipitation. Compared with the example 1, the mechanical property of the TPU material is improved but the heat resistance, the water resistance and the flame retardant grade are reduced without adding PDMS into the polyol of the comparative example 1; comparative example 2 does not add a synergistic flame retardant, has slightly higher mechanical properties, but has a reduced flame retardant rating; the TMP content in the chain extender of the comparative example 3 exceeds a critical value, so that the mechanical properties of the TPU material are reduced; TMP is not added into the chain extender of comparative example 4, so that the mechanical properties of the TPU material are poor; the isocyanate of comparative example 5 increases the content of HMDI, the mechanical properties of the TPU material are reduced, and the light transmittance of the TPU material is increased; the isocyanate of comparative example 6 uses a single component MDI, and the light transmittance of the TPU material is reduced; comparative example 7 only used a long biaxial twin screw production process, the mechanical properties of the TPU material were degraded.
Claims (10)
1. A high strength TPU material for a charging pile cable, characterized by: the material comprises the following raw materials in parts by weight:
50-70 parts of mixed polyol,
25-40 parts of isocyanate and the like,
5-10 parts of composite chain extender,
0.1 to 0.3 part of antioxidant,
0.05 to 0.2 part of hydrolysis resistant agent,
0.02-0.1 part of catalyst,
0.01 to 0.03 part of dispersing agent,
0.005-0.01 part of synergistic flame retardant,
0.05-0.3 part of ultraviolet absorber;
the mixed polyol is at least one of polycaprolactone diol and polytetramethylene ether glycol, and is mixed with end-hydroxybutyl-terminated polydimethylsiloxane;
the compound chain extender is prepared by compounding 85-99wt.% of 1, 4-butanediol and 1-15wt.% of trimethylolpropane;
the isocyanate is a mixture of 90-95wt.% diphenylmethane diisocyanate and 5-10wt.% dicyclohexylmethane diisocyanate;
the synergistic flame retardant is silane coupling agent modified nano Sb 2 O 3 And (3) powder.
2. The high strength TPU material for a charging pile cable according to claim 1, wherein: the number average molecular weight of the polycaprolactone diol and the polytetramethylene ether glycol is 500-2000; the number average molecular weight of the end-hydroxybutyl-terminated polydimethylsiloxane is 1500-2000.
3. The high strength TPU material for a charging pile cable according to claim 1, wherein: in the mixed polyol, the mass percentage of the end-hydroxybutyl-terminated polydimethylsiloxane is 5-15%.
4. The high strength TPU material for a charging pile cable according to claim 1, wherein: the silane coupling agent modifies nano Sb 2 O 3 Nano Sb in powder 2 O 3 The average particle diameter of the powder is between 30 and 50 nm.
5. The high strength TPU material for a charging pile cable according to claim 1, wherein: the antioxidant is phosphite antioxidant.
6. The high strength TPU material for a charging pile cable according to claim 1, wherein: the hydrolysis resistance agent is carbodiimide.
7. The high strength TPU material for a charging pile cable according to claim 1, wherein: the catalyst is an organotin catalyst.
8. The high strength TPU material for a charging pile cable according to claim 1, wherein: the dispersing agent is at least one of glyceryl monostearate, glyceryl tristearate, barium stearate and calcium stearate.
9. The high strength TPU material for a charging pile cable according to claim 1, wherein: the ultraviolet absorbent is at least one of N- (ethoxycarbonylphenyl) -N '-methyl-N' -phenylamidine, N- (ethoxycarbonylphenyl) -N '-ethyl-N' -phenylformamidine, phenyl o-hydroxybenzoate, 2- (2 '-hydroxy-5' -methylphenyl) benzotriazole, 2, 4-dihydroxybenzophenone, 2-hydroxy-4-methoxybenzophenone and 2-hydroxy-4-N-octoxybenzophenone.
10. A method of preparing a high strength TPU material for a charging pile cable according to any one of claims 1 to 9, characterised by: the method comprises the following steps:
adopting a two-section double-screw extruder connected with a middle double-shaft double-screw and a long double-shaft double-screw to carry out continuous polymerization reaction, firstly adding an antioxidant, a hydrolysis-resistant agent, a dispersing agent, a synergistic flame retardant and an ultraviolet absorbent into mixed polyol, and carrying out prepolymerization reaction with partial isocyanate and a catalyst in the middle double-shaft double-screw to obtain a prepolymer; and then conveying the prepolymer into a long double-shaft double-screw rod, carrying out polymerization reaction with the residual isocyanate and the composite chain extender, and carrying out underwater cutting granulation to obtain the high-strength TPU material for the charging pile cable.
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