JP2010539278A5 - - Google Patents

Info

Publication number

JP2010539278A5

JP2010539278A5 JP2010524622A JP2010524622A JP2010539278A5 JP 2010539278 A5 JP2010539278 A5 JP 2010539278A5 JP 2010524622 A JP2010524622 A JP 2010524622A JP 2010524622 A JP2010524622 A JP 2010524622A JP 2010539278 A5 JP2010539278 A5 JP 2010539278A5

Authority

JP

Japan

Prior art keywords

compound

ppm

sulfur

olefin

hydrocarbon

Prior art date

2008-09-12

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.)

Granted

Links

• Espacenet
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• 150000001875 compounds Chemical class 0.000 claims 14
• 239000000654 additive Substances 0.000 claims 11
• 230000000996 additive effect Effects 0.000 claims 11
• 239000004215 Carbon black (E152) Substances 0.000 claims 9
• 150000001336 alkenes Chemical class 0.000 claims 9
• 229930195733 hydrocarbon Natural products 0.000 claims 9
• 150000002430 hydrocarbons Chemical class 0.000 claims 9
• 239000000203 mixture Substances 0.000 claims 9
• JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 9
• 239000011541 reaction mixture Substances 0.000 claims 8
• 238000005260 corrosion Methods 0.000 claims 7
• 230000007797 corrosion Effects 0.000 claims 7
• NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims 6
• 229920002367 Polyisobutene Polymers 0.000 claims 6
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 6
• LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 claims 6
• HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 claims 5
• 238000000034 method Methods 0.000 claims 5
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
• 229940126062 Compound A Drugs 0.000 claims 4
• 229910001873 dinitrogen Inorganic materials 0.000 claims 4
• 239000007789 gas Substances 0.000 claims 4
• 230000002401 inhibitory effect Effects 0.000 claims 4
• OTYNBGDFCPCPOU-UHFFFAOYSA-N phosphane sulfane Chemical compound S.P[H] OTYNBGDFCPCPOU-UHFFFAOYSA-N 0.000 claims 4
• CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 claims 4
• 239000000126 substance Substances 0.000 claims 4
• 229910052717 sulfur Inorganic materials 0.000 claims 4
• 239000011593 sulfur Substances 0.000 claims 4
• 239000003112 inhibitor Substances 0.000 claims 3
• 230000005764 inhibitory process Effects 0.000 claims 3
• RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims 2
• IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 2
• 125000004432 carbon atom Chemical group C* 0.000 claims 2
• 239000010779 crude oil Substances 0.000 claims 2
• 238000004821 distillation Methods 0.000 claims 2
• 229910000037 hydrogen sulfide Inorganic materials 0.000 claims 2
• 239000002184 metal Substances 0.000 claims 2
• 238000010926 purge Methods 0.000 claims 2
• -1 thiophosphate compound Chemical group 0.000 claims 2
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
• GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 1
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 1
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
• 230000003197 catalytic effect Effects 0.000 claims 1
• 238000010438 heat treatment Methods 0.000 claims 1
• 229910052739 hydrogen Inorganic materials 0.000 claims 1
• 239000001257 hydrogen Substances 0.000 claims 1
• 229910052760 oxygen Chemical group 0.000 claims 1
• 239000001301 oxygen Chemical group 0.000 claims 1
• 230000001681 protective effect Effects 0.000 claims 1
• 238000003756 stirring Methods 0.000 claims 1
• SUEGWIXYCHISPX-UHFFFAOYSA-N sulfane trihydroxy(sulfanylidene)-lambda5-phosphane Chemical class OP(O)(O)=S.S SUEGWIXYCHISPX-UHFFFAOYSA-N 0.000 claims 1
• 150000003464 sulfur compounds Chemical class 0.000 claims 1