CA2484332A1 - Alkylaminosiloxanes as corrosion inhibitors - Google Patents

Info

Publication number

CA2484332A1

CA2484332A1 CA002484332A CA2484332A CA2484332A1 CA 2484332 A1 CA2484332 A1 CA 2484332A1 CA 002484332 A CA002484332 A CA 002484332A CA 2484332 A CA2484332 A CA 2484332A CA 2484332 A1 CA2484332 A1 CA 2484332A1

Authority

CA

Canada

Prior art keywords

c4alkyl

unsubstituted

substituted

independently

interrupted

Prior art date

2002-05-31

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.)

Abandoned

Links

• Espacenet
• Global Dossier
• CIPO
• Discuss

• 230000007797 corrosion Effects 0.000 title claims abstract description 51
• 238000005260 corrosion Methods 0.000 title claims abstract description 51
• 239000003112 inhibitor Substances 0.000 title claims description 22
• 239000000203 mixture Substances 0.000 claims abstract description 67
• 150000001875 compounds Chemical class 0.000 claims abstract description 65
• 239000005022 packaging material Substances 0.000 claims abstract description 4
• -1 C3-C8alkynyl Chemical group 0.000 claims description 113
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 62
• 229910052760 oxygen Inorganic materials 0.000 claims description 62
• 239000001301 oxygen Substances 0.000 claims description 62
• 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 51
• 229910052799 carbon Inorganic materials 0.000 claims description 48
• 229920001577 copolymer Polymers 0.000 claims description 42
• 125000000843 phenylene group Chemical class C1(=C(C=CC=C1)*)* 0.000 claims description 35
• 229910052739 hydrogen Inorganic materials 0.000 claims description 30
• 239000001257 hydrogen Substances 0.000 claims description 30
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 29
• 229910052751 metal Inorganic materials 0.000 claims description 20
• 239000002184 metal Substances 0.000 claims description 20
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 18
• 125000004432 carbon atom Chemical group C* 0.000 claims description 18
• 238000000034 method Methods 0.000 claims description 17
• 239000000654 additive Substances 0.000 claims description 14
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 14
• 150000002431 hydrogen Chemical group 0.000 claims description 12
• 239000004743 Polypropylene Substances 0.000 claims description 11
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 10
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 10
• 125000004956 cyclohexylene group Chemical group 0.000 claims description 10
• 229920001059 synthetic polymer Polymers 0.000 claims description 10
• 239000004698 Polyethylene Substances 0.000 claims description 9
• 150000001993 dienes Chemical class 0.000 claims description 9
• 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 8
• 125000004957 naphthylene group Chemical class 0.000 claims description 8
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• 239000000758 substrate Substances 0.000 claims description 7
• 125000000109 phenylethoxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])O* 0.000 claims description 6
• 150000005673 monoalkenes Chemical class 0.000 claims description 5
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• 239000011230 binding agent Substances 0.000 claims description 4
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
• 238000012545 processing Methods 0.000 claims description 4
• 239000003381 stabilizer Substances 0.000 claims description 4
• 125000000304 alkynyl group Chemical group 0.000 claims description 3
• 239000000969 carrier Substances 0.000 claims description 3
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• 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 3
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• 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
• 125000003031 C5-C7 cycloalkylene group Chemical group 0.000 claims 1
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• 125000000217 alkyl group Chemical group 0.000 description 9
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• 230000002401 inhibitory effect Effects 0.000 description 8
• GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 8
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• CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 6
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• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
• 239000002253 acid Substances 0.000 description 6
• 150000001252 acrylic acid derivatives Chemical class 0.000 description 6
• 125000003118 aryl group Chemical group 0.000 description 6
• DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 6
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• 239000000178 monomer Substances 0.000 description 6
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• 239000000047 product Substances 0.000 description 6
• 239000000243 solution Substances 0.000 description 6
• 230000000007 visual effect Effects 0.000 description 6
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
• BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 5
• 101150041968 CDC13 gene Proteins 0.000 description 5
• 239000004721 Polyphenylene oxide Substances 0.000 description 5
• HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 5
• 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 5
• 150000001721 carbon Chemical group 0.000 description 5
• 229920001519 homopolymer Polymers 0.000 description 5
• WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 5
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• 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 5
• 239000007787 solid Substances 0.000 description 5
• 239000012808 vapor phase Substances 0.000 description 5
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• BPXVHIRIPLPOPT-UHFFFAOYSA-N 1,3,5-tris(2-hydroxyethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound OCCN1C(=O)N(CCO)C(=O)N(CCO)C1=O BPXVHIRIPLPOPT-UHFFFAOYSA-N 0.000 description 4
• ALVZNPYWJMLXKV-UHFFFAOYSA-N 1,9-Nonanediol Chemical compound OCCCCCCCCCO ALVZNPYWJMLXKV-UHFFFAOYSA-N 0.000 description 4
• KXPXKNBDCUOENF-UHFFFAOYSA-N 2-(Octylthio)ethanol Chemical compound CCCCCCCCSCCO KXPXKNBDCUOENF-UHFFFAOYSA-N 0.000 description 4
• ZPIRWAHWDCHWLM-UHFFFAOYSA-N 2-dodecylsulfanylethanol Chemical compound CCCCCCCCCCCCSCCO ZPIRWAHWDCHWLM-UHFFFAOYSA-N 0.000 description 4
• CKPKHTKLLYPGFM-UHFFFAOYSA-N 6,6-dimethylheptane-1,1-diol Chemical compound CC(CCCCC(O)O)(C)C CKPKHTKLLYPGFM-UHFFFAOYSA-N 0.000 description 4
• CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
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• 239000007983 Tris buffer Substances 0.000 description 4
• WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
• 125000003342 alkenyl group Chemical group 0.000 description 4
• 150000008064 anhydrides Chemical class 0.000 description 4
• 239000012964 benzotriazole Substances 0.000 description 4
• FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 4
• 238000006243 chemical reaction Methods 0.000 description 4
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• KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 4
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• 238000010998 test method Methods 0.000 description 4
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• 125000001931 aliphatic group Chemical group 0.000 description 3
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• 125000000753 cycloalkyl group Chemical group 0.000 description 3
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• LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 3
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• 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([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 description 3
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• BWJKLDGAAPQXGO-UHFFFAOYSA-N 2,2,6,6-tetramethyl-4-octadecoxypiperidine Chemical compound CCCCCCCCCCCCCCCCCCOC1CC(C)(C)NC(C)(C)C1 BWJKLDGAAPQXGO-UHFFFAOYSA-N 0.000 description 2
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