ES2757957T3 - Tubo de poliolefina - Google Patents
Tubo de poliolefina Download PDFInfo
- Publication number
- ES2757957T3 ES2757957T3 ES15718476T ES15718476T ES2757957T3 ES 2757957 T3 ES2757957 T3 ES 2757957T3 ES 15718476 T ES15718476 T ES 15718476T ES 15718476 T ES15718476 T ES 15718476T ES 2757957 T3 ES2757957 T3 ES 2757957T3
- Authority
- ES
- Spain
- Prior art keywords
- tube
- alkyl
- optionally
- alkenyl
- photoinitiator
- 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.)
- Active
Links
- 229920000098 polyolefin Polymers 0.000 title claims abstract description 58
- 229920000642 polymer Polymers 0.000 claims abstract description 74
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 57
- 125000000304 alkynyl group Chemical group 0.000 claims abstract description 46
- 125000000262 haloalkenyl group Chemical group 0.000 claims abstract description 38
- 125000000232 haloalkynyl group Chemical group 0.000 claims abstract description 36
- 150000001875 compounds Chemical class 0.000 claims abstract description 33
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 23
- 125000001475 halogen functional group Chemical group 0.000 claims abstract 5
- 125000000217 alkyl group Chemical group 0.000 claims description 114
- 238000000034 method Methods 0.000 claims description 93
- 238000004132 cross linking Methods 0.000 claims description 65
- -1 polyethylene Polymers 0.000 claims description 57
- 239000004698 Polyethylene Substances 0.000 claims description 47
- 229920000573 polyethylene Polymers 0.000 claims description 47
- 239000000203 mixture Substances 0.000 claims description 46
- 239000003963 antioxidant agent Substances 0.000 claims description 32
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 28
- 239000003651 drinking water Substances 0.000 claims description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 27
- 238000001125 extrusion Methods 0.000 claims description 26
- 235000020188 drinking water Nutrition 0.000 claims description 25
- NPFYZDNDJHZQKY-UHFFFAOYSA-N 4-Hydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 NPFYZDNDJHZQKY-UHFFFAOYSA-N 0.000 claims description 23
- 239000003795 chemical substances by application Substances 0.000 claims description 21
- 125000001188 haloalkyl group Chemical group 0.000 claims description 19
- 230000003078 antioxidant effect Effects 0.000 claims description 18
- 239000004611 light stabiliser Substances 0.000 claims description 17
- 238000004519 manufacturing process Methods 0.000 claims description 17
- 150000001412 amines Chemical class 0.000 claims description 15
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 15
- 239000012965 benzophenone Substances 0.000 claims description 14
- 229920002857 polybutadiene Polymers 0.000 claims description 12
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 11
- 230000005855 radiation Effects 0.000 claims description 10
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 8
- 239000005062 Polybutadiene Substances 0.000 claims description 8
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 claims description 8
- 238000002156 mixing Methods 0.000 claims description 8
- 239000002530 phenolic antioxidant Substances 0.000 claims description 7
- 239000004743 Polypropylene Substances 0.000 claims description 6
- 229920001155 polypropylene Polymers 0.000 claims description 6
- 230000001678 irradiating effect Effects 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 4
- 125000004386 diacrylate group Chemical group 0.000 claims description 4
- 229920001748 polybutylene Polymers 0.000 claims description 4
- 229920002635 polyurethane Polymers 0.000 claims description 4
- 239000004814 polyurethane Substances 0.000 claims description 4
- MLZBRARCTFICSV-UHFFFAOYSA-N 4-benzoylbenzaldehyde Chemical compound C1=CC(C=O)=CC=C1C(=O)C1=CC=CC=C1 MLZBRARCTFICSV-UHFFFAOYSA-N 0.000 claims description 3
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 3
- 239000003921 oil Substances 0.000 claims description 2
- 229920002121 Hydroxyl-terminated polybutadiene Polymers 0.000 claims 2
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 claims 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 claims 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 238000012360 testing method Methods 0.000 description 68
- 230000008569 process Effects 0.000 description 49
- 229920003020 cross-linked polyethylene Polymers 0.000 description 39
- 239000004703 cross-linked polyethylene Substances 0.000 description 39
- 239000003381 stabilizer Substances 0.000 description 33
- 239000000463 material Substances 0.000 description 32
- 239000000654 additive Substances 0.000 description 28
- 238000002386 leaching Methods 0.000 description 24
- 238000009472 formulation Methods 0.000 description 23
- 239000000047 product Substances 0.000 description 20
- 239000000126 substance Substances 0.000 description 20
- 239000006057 Non-nutritive feed additive Substances 0.000 description 15
- 230000007774 longterm Effects 0.000 description 15
- 229920005989 resin Polymers 0.000 description 12
- 239000011347 resin Substances 0.000 description 12
- 125000003386 piperidinyl group Chemical group 0.000 description 11
- 125000001931 aliphatic group Chemical group 0.000 description 10
- 229910052801 chlorine Inorganic materials 0.000 description 10
- 239000000460 chlorine Substances 0.000 description 10
- 229920001903 high density polyethylene Polymers 0.000 description 10
- 239000004700 high-density polyethylene Substances 0.000 description 10
- JLZIIHMTTRXXIN-UHFFFAOYSA-N 2-(2-hydroxy-4-methoxybenzoyl)benzoic acid Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1C(O)=O JLZIIHMTTRXXIN-UHFFFAOYSA-N 0.000 description 9
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 238000009826 distribution Methods 0.000 description 9
- 238000002347 injection Methods 0.000 description 9
- 239000007924 injection Substances 0.000 description 9
- 239000011159 matrix material Substances 0.000 description 9
- 230000001590 oxidative effect Effects 0.000 description 9
- 238000004458 analytical method Methods 0.000 description 8
- 238000013461 design Methods 0.000 description 8
- 239000000284 extract Substances 0.000 description 8
- 239000012530 fluid Substances 0.000 description 8
- 229920003023 plastic Polymers 0.000 description 8
- 239000004033 plastic Substances 0.000 description 8
- 238000012545 processing Methods 0.000 description 7
- 229920006395 saturated elastomer Polymers 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000001816 cooling Methods 0.000 description 6
- 125000004122 cyclic group Chemical group 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 125000000524 functional group Chemical group 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 6
- 229920002959 polymer blend Polymers 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
- 0 *c(cc1)ccc1C(c1ccc(*)cc1)=O Chemical compound *c(cc1)ccc1C(c1ccc(*)cc1)=O 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 230000008901 benefit Effects 0.000 description 5
- 125000000753 cycloalkyl group Chemical group 0.000 description 5
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 230000006698 induction Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 238000010525 oxidative degradation reaction Methods 0.000 description 5
- 150000003254 radicals Chemical class 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 238000010998 test method Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 4
- 239000000356 contaminant Substances 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 238000010894 electron beam technology Methods 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- 239000007800 oxidant agent Substances 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 230000006641 stabilisation Effects 0.000 description 4
- 238000011105 stabilization Methods 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- 229920001169 thermoplastic Polymers 0.000 description 4
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 4
- 239000002699 waste material Substances 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 238000003556 assay Methods 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 229920006037 cross link polymer Polymers 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 150000002118 epoxides Chemical class 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 238000013508 migration Methods 0.000 description 3
- 230000005012 migration Effects 0.000 description 3
- 239000002105 nanoparticle Substances 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 description 3
- 229910000077 silane Inorganic materials 0.000 description 3
- 239000010802 sludge Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 230000035882 stress Effects 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- HQUPVZXXKOHWPK-UHFFFAOYSA-N (4-decoxyphenyl)-phenylmethanone Chemical compound C1=CC(OCCCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 HQUPVZXXKOHWPK-UHFFFAOYSA-N 0.000 description 2
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- LEJBBGNFPAFPKQ-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOC(=O)C=C LEJBBGNFPAFPKQ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 2
- 238000003848 UV Light-Curing Methods 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 150000008366 benzophenones Chemical class 0.000 description 2
- WTAJUZVRCDEXDL-UHFFFAOYSA-N bis(4-hexoxyphenyl)methanone Chemical compound C1=CC(OCCCCCC)=CC=C1C(=O)C1=CC=C(OCCCCCC)C=C1 WTAJUZVRCDEXDL-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 235000012206 bottled water Nutrition 0.000 description 2
- IAQRGUVFOMOMEM-UHFFFAOYSA-N but-2-ene Chemical compound CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 2
- 150000001721 carbon Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
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- 230000006866 deterioration Effects 0.000 description 2
- 230000005281 excited state Effects 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 229920002313 fluoropolymer Polymers 0.000 description 2
- 239000004811 fluoropolymer Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 230000002706 hydrostatic effect Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 230000000977 initiatory effect Effects 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 229920001179 medium density polyethylene Polymers 0.000 description 2
- 239000004701 medium-density polyethylene Substances 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 125000003367 polycyclic group Chemical group 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 238000010094 polymer processing Methods 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 239000008247 solid mixture Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 238000010561 standard procedure Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- XUAHXVVAWLNXSW-UHFFFAOYSA-N (4-hexoxyphenyl)-phenylmethanone Chemical compound C1=CC(OCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 XUAHXVVAWLNXSW-UHFFFAOYSA-N 0.000 description 1
- IOHOTYAESDYADZ-UHFFFAOYSA-N (4-octadecoxyphenyl)-phenylmethanone Chemical compound C1=CC(OCCCCCCCCCCCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 IOHOTYAESDYADZ-UHFFFAOYSA-N 0.000 description 1
- MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 1
- VNQXSTWCDUXYEZ-UHFFFAOYSA-N 1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione Chemical compound C1CC2(C)C(=O)C(=O)C1C2(C)C VNQXSTWCDUXYEZ-UHFFFAOYSA-N 0.000 description 1
- ZDQNWDNMNKSMHI-UHFFFAOYSA-N 1-[2-(2-prop-2-enoyloxypropoxy)propoxy]propan-2-yl prop-2-enoate Chemical compound C=CC(=O)OC(C)COC(C)COCC(C)OC(=O)C=C ZDQNWDNMNKSMHI-UHFFFAOYSA-N 0.000 description 1
- MYMSJFSOOQERIO-UHFFFAOYSA-N 1-bromodecane Chemical compound CCCCCCCCCCBr MYMSJFSOOQERIO-UHFFFAOYSA-N 0.000 description 1
- 125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 description 1
- 125000006039 1-hexenyl group Chemical group 0.000 description 1
- 125000006023 1-pentenyl group Chemical group 0.000 description 1
- XEZNGIUYQVAUSS-UHFFFAOYSA-N 18-crown-6 Chemical compound C1COCCOCCOCCOCCOCCO1 XEZNGIUYQVAUSS-UHFFFAOYSA-N 0.000 description 1
- 150000003923 2,5-pyrrolediones Chemical class 0.000 description 1
- ZWBJYYOZBDHRMI-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethanol;prop-2-enoic acid Chemical compound OC(=O)C=C.OCCOCCO ZWBJYYOZBDHRMI-UHFFFAOYSA-N 0.000 description 1
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 1
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
- GTELLNMUWNJXMQ-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical class OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.CCC(CO)(CO)CO GTELLNMUWNJXMQ-UHFFFAOYSA-N 0.000 description 1
- 125000006040 2-hexenyl group Chemical group 0.000 description 1
- 125000006024 2-pentenyl group Chemical group 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 1
- MXRGSJAOLKBZLU-UHFFFAOYSA-N 3-ethenylazepan-2-one Chemical compound C=CC1CCCCNC1=O MXRGSJAOLKBZLU-UHFFFAOYSA-N 0.000 description 1
- 125000006041 3-hexenyl group Chemical group 0.000 description 1
- RXNYJUSEXLAVNQ-UHFFFAOYSA-N 4,4'-Dihydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1 RXNYJUSEXLAVNQ-UHFFFAOYSA-N 0.000 description 1
- SWZOQAGVRGQLDV-UHFFFAOYSA-N 4-[2-(4-hydroxy-2,2,6,6-tetramethylpiperidin-1-yl)ethoxy]-4-oxobutanoic acid Chemical compound CC1(C)CC(O)CC(C)(C)N1CCOC(=O)CCC(O)=O SWZOQAGVRGQLDV-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
- 241000239290 Araneae Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 238000000305 Fourier transform infrared microscopy Methods 0.000 description 1
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- 229920010741 Ultra High Molecular Weight Polyethylene (UHMWPE) Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- FHLPGTXWCFQMIU-UHFFFAOYSA-N [4-[2-(4-prop-2-enoyloxyphenyl)propan-2-yl]phenyl] prop-2-enoate Chemical class C=1C=C(OC(=O)C=C)C=CC=1C(C)(C)C1=CC=C(OC(=O)C=C)C=C1 FHLPGTXWCFQMIU-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 231100000569 acute exposure Toxicity 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
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- 238000000113 differential scanning calorimetry Methods 0.000 description 1
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- BTVWZWFKMIUSGS-UHFFFAOYSA-N dimethylethyleneglycol Natural products CC(C)(O)CO BTVWZWFKMIUSGS-UHFFFAOYSA-N 0.000 description 1
- GKHRLTCUMXVTAV-UHFFFAOYSA-N dimoracin Chemical compound C1=C(O)C=C2OC(C3=CC(O)=C(C(=C3)O)C3C4C(C5=C(O)C=C(C=C5O3)C=3OC5=CC(O)=CC=C5C=3)C=C(CC4(C)C)C)=CC2=C1 GKHRLTCUMXVTAV-UHFFFAOYSA-N 0.000 description 1
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- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
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- LEZHOUZKYMZPAO-UHFFFAOYSA-N ethene prop-2-enoic acid Chemical compound C=C.C=C.C=C.OC(=O)C=C.OC(=O)C=C LEZHOUZKYMZPAO-UHFFFAOYSA-N 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
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- 125000005843 halogen group Chemical group 0.000 description 1
- 239000008236 heating water Substances 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/28—Treatment by wave energy or particle radiation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/07—Aldehydes; Ketones
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16L—PIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
- F16L9/00—Rigid pipes
- F16L9/12—Rigid pipes of plastics with or without reinforcement
-
- 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
- B29C35/00—Heating, cooling or curing, e.g. crosslinking or vulcanising; Apparatus therefor
- B29C35/02—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould
- B29C35/08—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation
- B29C35/0805—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using electromagnetic radiation
- B29C2035/0827—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using electromagnetic radiation using UV radiation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/04—Homopolymers or copolymers of ethene
- C08J2323/06—Polyethene
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
- C08K5/105—Esters; Ether-esters of monocarboxylic acids with phenols
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
- C08K5/3435—Piperidines
Landscapes
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Engineering & Computer Science (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Rigid Pipes And Flexible Pipes (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Heating, Cooling, Or Curing Plastics Or The Like In General (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461983062P | 2014-04-23 | 2014-04-23 | |
| PCT/EP2015/058663 WO2015162155A1 (en) | 2014-04-23 | 2015-04-22 | Polyolefin pipe |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2757957T3 true ES2757957T3 (es) | 2020-04-30 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES15718476T Active ES2757957T3 (es) | 2014-04-23 | 2015-04-22 | Tubo de poliolefina |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US10519286B2 (enExample) |
| EP (1) | EP3134669B1 (enExample) |
| JP (1) | JP6698548B2 (enExample) |
| CA (1) | CA2945412C (enExample) |
| DK (1) | DK3134669T3 (enExample) |
| EA (1) | EA032099B1 (enExample) |
| ES (1) | ES2757957T3 (enExample) |
| GB (1) | GB2525453A (enExample) |
| PL (1) | PL3134669T3 (enExample) |
| PT (1) | PT3134669T (enExample) |
| WO (1) | WO2015162155A1 (enExample) |
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| FR3045641B1 (fr) * | 2015-12-22 | 2021-04-30 | Bluestar Silicones France | Utilisation d'un systeme photoamorceur de type ii pour la reticulation de compositions silicones |
| CA2977581A1 (en) | 2016-09-02 | 2018-03-02 | Zurn Industries, Llc | Injection molded cold-expansion compression collar |
| US11543065B2 (en) | 2016-09-02 | 2023-01-03 | Zurn Industries, Llc | Extruded cold-expansion compression collar |
| US11541581B2 (en) | 2016-09-02 | 2023-01-03 | Zurn Industries, Llc | Injection molded cold-expansion compression collar |
| US11054076B2 (en) | 2016-11-04 | 2021-07-06 | Zurn Industries, Llc | Reinforcing ring with sleeve |
| US11667762B2 (en) * | 2017-08-29 | 2023-06-06 | The General Hospital Corporation | UV-initiated reactions in polymeric materials |
| IL257535B (en) * | 2018-02-14 | 2020-01-30 | N3 Coat Ltd | Benzophenone compounds as light catalysts for polyolefins |
| CN113795368B (zh) | 2019-05-02 | 2025-03-07 | Sabic环球技术有限责任公司 | 输送氯化水的管 |
| JP7477954B2 (ja) * | 2019-10-16 | 2024-05-02 | 旭化成アドバンス株式会社 | コンクリート圧送方法 |
| CN111022786B (zh) * | 2019-12-30 | 2021-06-15 | 安徽杰蓝特新材料有限公司 | 一种玻纤增强pe给水管及其制备方法 |
| WO2021148352A1 (en) | 2020-01-21 | 2021-07-29 | Sabic Global Technologies B.V. | Pipe for transport of water containing chlorinated disinfectant |
| WO2022219672A1 (ja) * | 2021-04-12 | 2022-10-20 | 旭化成アドバンス株式会社 | コンクリート圧送管 |
| CN117597388B (zh) | 2021-07-08 | 2025-09-19 | 北欧化工公司 | 用于生产交联聚乙烯（pex）的聚乙烯 |
| GB2607979B (en) * | 2021-11-30 | 2024-01-31 | Wavin Bv | Multi-layered pipe |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4310650A (en) * | 1980-03-03 | 1982-01-12 | California Institute Of Technology | Ultraviolet absorbing copolymers |
| IN164745B (enExample) | 1984-05-11 | 1989-05-20 | Stamicarbon | |
| JPH03180323A (ja) | 1989-12-08 | 1991-08-06 | Toyo Echo Kk | 熱収縮性蓋の製造方法 |
| JPH03287632A (ja) * | 1990-04-05 | 1991-12-18 | Fujikura Ltd | 架橋ポリオレフィン成形物の製法 |
| SE500503C2 (sv) | 1990-12-07 | 1994-07-04 | Inst Polymerutveckling Ab | Förfarande och bestrålningsenhet för kontinuerlig tvärbindning av polyeten |
| US5299885A (en) * | 1992-08-14 | 1994-04-05 | Aquapore Moisture Systems, Inc. | Stabilized porous pipe |
| FR2710344B1 (fr) | 1993-09-21 | 1995-11-17 | Inst Francais Du Petrole | Compositions de polyéthylènes réticulables, utilisées notamment pour la fabrication de tubes et de gaines flexibles. |
| DE4404041C1 (de) | 1994-02-09 | 1995-03-23 | Ruesch Willy Ag | Polymermaterial von medizinischen Instrumenten und Verfahren zur Herstellung des Polymermaterials |
| NL1008960C2 (nl) | 1998-04-22 | 1999-10-25 | Wavin Bv | Kunststofbuis met een uit meerdere lagen samengestelde wand. |
| WO2000022334A1 (en) * | 1998-10-09 | 2000-04-20 | Sekisui Chemical Co., Ltd. | Composite high-pressure pipe and method of joining same |
| AR023110A1 (es) | 1999-03-22 | 2002-09-04 | Loctite Corp | Articulos roscados con revestimiento deformable curado sobre los mismos |
| CA2372056A1 (en) * | 1999-05-14 | 2000-11-23 | Morgan Mark Hughes | Highly crystalline eaodm interpolymers |
| US6696154B2 (en) * | 1999-07-27 | 2004-02-24 | Pirelli Cavi E Sistemi S.P.A. | Cable, in particular for transport or distribution of electrical energy and insulating composition |
| JP2001074182A (ja) | 1999-09-07 | 2001-03-23 | Toyo Tire & Rubber Co Ltd | 可とう伸縮継手の製造方法 |
| DE60138206D1 (de) * | 2000-09-11 | 2009-05-14 | Sekisui Seikei Ltd | Verfahren zur herstellung einer verstreckten folie aus polyolefin |
| JP2002113766A (ja) * | 2000-10-05 | 2002-04-16 | Sekisui Chem Co Ltd | ポリエチレン管の製造方法およびこの製造方法に用いる金型 |
| DE10058290A1 (de) | 2000-11-23 | 2002-05-29 | Basf Ag | Verfahren zur Stabilisierung von Polyolefinen |
| IL140541A0 (en) | 2000-12-25 | 2002-02-10 | Syfan Saad 99 Ltd | Improved process for the manufacture of thermoplastic shrink films |
| JP2002348479A (ja) * | 2001-05-24 | 2002-12-04 | Jsr Corp | 放射線架橋性ポリマー組成物 |
| US6652943B2 (en) | 2001-06-04 | 2003-11-25 | Saint-Gobain Performance Plastics Corporation | Multilayer polymeric article with intercrosslinked polymer layers and method of making same |
| GB0125099D0 (en) | 2001-10-18 | 2001-12-12 | Coates Brothers Plc | Multi-functional photoinitiators |
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| DE102004061981A1 (de) | 2004-12-23 | 2006-07-06 | Rehau Ag + Co. | Materialzusammensetzung zur UV-Vernetzung |
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| EP2992044B1 (en) | 2013-05-03 | 2022-01-12 | Uponor Innovation AB | Polyolefin pipe |
-
2014
- 2014-07-08 GB GB1412092.7A patent/GB2525453A/en not_active Withdrawn
-
2015
- 2015-04-22 JP JP2016564043A patent/JP6698548B2/ja active Active
- 2015-04-22 PL PL15718476T patent/PL3134669T3/pl unknown
- 2015-04-22 WO PCT/EP2015/058663 patent/WO2015162155A1/en not_active Ceased
- 2015-04-22 US US15/304,597 patent/US10519286B2/en active Active
- 2015-04-22 EA EA201692133A patent/EA032099B1/ru not_active IP Right Cessation
- 2015-04-22 ES ES15718476T patent/ES2757957T3/es active Active
- 2015-04-22 CA CA2945412A patent/CA2945412C/en active Active
- 2015-04-22 EP EP15718476.3A patent/EP3134669B1/en active Active
- 2015-04-22 PT PT157184763T patent/PT3134669T/pt unknown
- 2015-04-22 DK DK15718476T patent/DK3134669T3/da active
Also Published As
| Publication number | Publication date |
|---|---|
| PT3134669T (pt) | 2019-11-29 |
| EP3134669B1 (en) | 2019-09-04 |
| CA2945412C (en) | 2023-02-21 |
| US20170114193A1 (en) | 2017-04-27 |
| JP6698548B2 (ja) | 2020-05-27 |
| EA201692133A1 (ru) | 2017-04-28 |
| DK3134669T3 (da) | 2019-11-25 |
| GB201412092D0 (en) | 2014-08-20 |
| JP2017519851A (ja) | 2017-07-20 |
| GB2525453A (en) | 2015-10-28 |
| PL3134669T3 (pl) | 2020-02-28 |
| EP3134669A1 (en) | 2017-03-01 |
| WO2015162155A1 (en) | 2015-10-29 |
| US10519286B2 (en) | 2019-12-31 |
| CA2945412A1 (en) | 2015-10-29 |
| EA032099B1 (ru) | 2019-04-30 |
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