JP2004533516A - 高有機酸性度を有する原油の精製方法 - Google Patents

高有機酸性度を有する原油の精製方法 Download PDF

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Publication number: JP2004533516A
Authority: JP; Japan
Prior art keywords: crude oil; compound; formula; ethanolamine; hydroxy
Prior art date: 2001-06-01
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.): Pending

Application number

JP2003500184A

Other languages

English (en)

Japanese (ja)

Inventor

ポールマルドナド

ロランバルベレ

ルイジュヌボワ

アランカトロ

Original Assignee

トタル・フランス

Priority date (The priority date 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 date listed.)

2001-06-01

Filing date

2002-05-31

Publication date

2004-11-04

2002-05-31 Application filed by トタル・フランス filed Critical トタル・フランス

2004-11-04 Publication of JP2004533516A publication Critical patent/JP2004533516A/ja

Status Pending legal-status Critical Current

Links

239000010779 crude oil Substances 0.000 title claims abstract description 53
238000000034 method Methods 0.000 title claims abstract description 40
238000007670 refining Methods 0.000 title description 6
150000001875 compounds Chemical class 0.000 claims abstract description 26
-1 nitride compound Chemical class 0.000 claims abstract description 16
238000004821 distillation Methods 0.000 claims abstract description 15
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 10
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 5
238000004519 manufacturing process Methods 0.000 claims abstract description 4
238000005121 nitriding Methods 0.000 claims abstract description 3
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 16
125000000217 alkyl group Chemical group 0.000 claims description 8
150000001412 amines Chemical class 0.000 claims description 5
238000010438 heat treatment Methods 0.000 claims description 5
150000003335 secondary amines Chemical group 0.000 claims description 5
VJWZYGQIJWDACM-UHFFFAOYSA-N 2-(2-methylpropylamino)ethanol Chemical compound CC(C)CNCCO VJWZYGQIJWDACM-UHFFFAOYSA-N 0.000 claims description 4
BCLSJHWBDUYDTR-UHFFFAOYSA-N 2-(propylamino)ethanol Chemical compound CCCNCCO BCLSJHWBDUYDTR-UHFFFAOYSA-N 0.000 claims description 4
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 4
LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 claims description 4
229940043276 diisopropanolamine Drugs 0.000 claims description 4
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
UNQGVFMDTATOTF-UHFFFAOYSA-N n-(2-aminobutyl)hydroxylamine Chemical compound CCC(N)CNO UNQGVFMDTATOTF-UHFFFAOYSA-N 0.000 claims description 3
150000003141 primary amines Chemical class 0.000 claims description 3
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 claims description 3
KQIXMZWXFFHRAQ-UHFFFAOYSA-N 1-(2-hydroxybutylamino)butan-2-ol Chemical compound CCC(O)CNCC(O)CC KQIXMZWXFFHRAQ-UHFFFAOYSA-N 0.000 claims description 2
VHQWELIDTIYJIJ-UHFFFAOYSA-N 2-(3-methylbutylamino)ethanol Chemical compound CC(C)CCNCCO VHQWELIDTIYJIJ-UHFFFAOYSA-N 0.000 claims description 2
LJDSTRZHPWMDPG-UHFFFAOYSA-N 2-(butylamino)ethanol Chemical compound CCCCNCCO LJDSTRZHPWMDPG-UHFFFAOYSA-N 0.000 claims description 2
SALYKAIZVOFAEJ-UHFFFAOYSA-N 2-(pentylamino)ethanol Chemical compound CCCCCNCCO SALYKAIZVOFAEJ-UHFFFAOYSA-N 0.000 claims description 2
KRGXWTOLFOPIKV-UHFFFAOYSA-N 3-(methylamino)propan-1-ol Chemical compound CNCCCO KRGXWTOLFOPIKV-UHFFFAOYSA-N 0.000 claims description 2
OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 claims description 2
TWLDZIZAUAEFBE-UHFFFAOYSA-N n-(ethylamino)hydroxylamine Chemical compound CCNNO TWLDZIZAUAEFBE-UHFFFAOYSA-N 0.000 claims description 2
150000004985 diamines Chemical class 0.000 claims 2
125000003277 amino group Chemical group 0.000 claims 1
238000011033 desalting Methods 0.000 claims 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
150000003512 tertiary amines Chemical group 0.000 claims 1
150000007524 organic acids Chemical class 0.000 abstract description 5
238000010586 diagram Methods 0.000 abstract description 4
230000003472 neutralizing effect Effects 0.000 abstract description 4
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 abstract 1
239000003921 oil Substances 0.000 description 12
150000001408 amides Chemical class 0.000 description 11
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 description 10
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 7
150000001735 carboxylic acids Chemical class 0.000 description 7
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
230000000694 effects Effects 0.000 description 6
230000008569 process Effects 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 5
238000005260 corrosion Methods 0.000 description 4
230000007797 corrosion Effects 0.000 description 4
238000000605 extraction Methods 0.000 description 4
238000002329 infrared spectrum Methods 0.000 description 4
239000003208 petroleum Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
229910021529 ammonia Inorganic materials 0.000 description 3
238000004458 analytical method Methods 0.000 description 3
150000002430 hydrocarbons Chemical class 0.000 description 3
125000005608 naphthenic acid group Chemical group 0.000 description 3
235000005985 organic acids Nutrition 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
230000002378 acidificating effect Effects 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000008901 benefit Effects 0.000 description 2
230000008859 change Effects 0.000 description 2
239000004927 clay Substances 0.000 description 2
238000010612 desalination reaction Methods 0.000 description 2
229940031098 ethanolamine Drugs 0.000 description 2
239000007791 liquid phase Substances 0.000 description 2
230000001050 lubricating effect Effects 0.000 description 2
239000000203 mixture Substances 0.000 description 2
238000006386 neutralization reaction Methods 0.000 description 2
239000012071 phase Substances 0.000 description 2
230000008929 regeneration Effects 0.000 description 2
238000011069 regeneration method Methods 0.000 description 2
125000001302 tertiary amino group Chemical group 0.000 description 2
239000004215 Carbon black (E152) Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
230000002411 adverse Effects 0.000 description 1
230000009435 amidation Effects 0.000 description 1
238000007112 amidation reaction Methods 0.000 description 1
238000010640 amide synthesis reaction Methods 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
235000011114 ammonium hydroxide Nutrition 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
238000004737 colorimetric analysis Methods 0.000 description 1
230000008034 disappearance Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
230000003203 everyday effect Effects 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
230000006872 improvement Effects 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
238000005461 lubrication Methods 0.000 description 1
239000012046 mixed solvent Substances 0.000 description 1
239000003129 oil well Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
150000003138 primary alcohols Chemical class 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000004611 spectroscopical analysis Methods 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1

Images

Classifications

- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G11/00—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G11/14—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts
- C10G11/18—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts according to the "fluidised-bed" technique
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G21/00—Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents
- C10G21/06—Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents characterised by the solvent used
- C10G21/12—Organic compounds only
- C10G21/20—Nitrogen-containing compounds
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
- C10G29/20—Organic compounds not containing metal atoms
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/02—Gasoline

Landscapes

Chemical & Material Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP2003500184A 2001-06-01 2002-05-31 高有機酸性度を有する原油の精製方法 Pending JP2004533516A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR0107247A FR2825369B1 (fr)	2001-06-01	2001-06-01	Procede de traitement de petrole bruts a acidite organique elevee
PCT/FR2002/001837 WO2002097014A1 (fr)	2001-06-01	2002-05-31	Procede de raffinage de petroles bruts a acidite organique elevee

Publications (1)

Publication Number	Publication Date
JP2004533516A true JP2004533516A (ja)	2004-11-04

Family

ID=8863899

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP2003500184A Pending JP2004533516A (ja)	2001-06-01	2002-05-31	高有機酸性度を有する原油の精製方法

Country Status (9)

Country	Link
US (1)	US20040134838A1 (fr)
EP (1)	EP1397468A1 (fr)
JP (1)	JP2004533516A (fr)
CA (1)	CA2452327C (fr)
FR (1)	FR2825369B1 (fr)
NO (1)	NO20035345D0 (fr)
OA (1)	OA12611A (fr)
WO (1)	WO2002097014A1 (fr)
ZA (1)	ZA200308957B (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US20100155304A1 (en) *	2008-12-23	2010-06-24	Her Majesty The Queen In Right Of Canada As Represented	Treatment of hydrocarbons containing acids
US9670423B1 (en)	2013-03-11	2017-06-06	Sochem Solutions, Inc.	SoNap unit : portable naphthenic acid springing unit

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2186249A (en) *	1939-01-17	1940-01-09	Tide Water Associated Oil Comp	Process of recovering organic acids
US2424158A (en) *	1944-09-20	1947-07-15	Standard Oil Dev Co	Process of refining a petroleum oil containing naphthenic acids
FR2112036A1 (en) *	1970-07-24	1972-06-16	Gamlen Naintre Sa	Crude oil treatment compsn - contg surfactant(s) and alcohol(s),amide(s) or phenol(s)
US4589979A (en) *	1985-08-22	1986-05-20	Nalco Chemical Company	Upgrading heavy gas oils
US5965785A (en) *	1993-09-28	1999-10-12	Nalco/Exxon Energy Chemicals, L.P.	Amine blend neutralizers for refinery process corrosion
US5961821A (en) *	1998-03-27	1999-10-05	Exxon Research And Engineering Co	Removal of naphthenic acids in crude oils and distillates
US6096196A (en) *	1998-03-27	2000-08-01	Exxon Research And Engineering Co.	Removal of naphthenic acids in crude oils and distillates

2001
- 2001-06-01 FR FR0107247A patent/FR2825369B1/fr not_active Expired - Fee Related
2002
- 2002-05-31 CA CA2452327A patent/CA2452327C/fr not_active Expired - Fee Related
- 2002-05-31 EP EP02743342A patent/EP1397468A1/fr not_active Withdrawn
- 2002-05-31 WO PCT/FR2002/001837 patent/WO2002097014A1/fr active Application Filing
- 2002-05-31 US US10/477,905 patent/US20040134838A1/en not_active Abandoned
- 2002-05-31 OA OA1200300307A patent/OA12611A/en unknown
- 2002-05-31 JP JP2003500184A patent/JP2004533516A/ja active Pending
2003
- 2003-11-18 ZA ZA200308957A patent/ZA200308957B/en unknown
- 2003-12-01 NO NO20035345A patent/NO20035345D0/no not_active Application Discontinuation

Also Published As

Publication number	Publication date
EP1397468A1 (fr)	2004-03-17
FR2825369A1 (fr)	2002-12-06
NO20035345D0 (no)	2003-12-01
FR2825369B1 (fr)	2005-04-15
US20040134838A1 (en)	2004-07-15
WO2002097014A1 (fr)	2002-12-05
ZA200308957B (en)	2004-09-16
CA2452327C (fr)	2010-06-29
OA12611A (en)	2006-06-09
CA2452327A1 (fr)	2002-12-05

Legal Events

Date	Code	Title	Description
2005-05-12	A621	Written request for application examination	Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20050511
2008-01-23	A131	Notification of reasons for refusal	Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20080122
2008-04-05	A601	Written request for extension of time	Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20080404
2008-04-16	A602	Written permission of extension of time	Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20080415
2008-05-21	A521	Request for written amendment filed	Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20080520
2009-09-02	A02	Decision of refusal	Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20090901

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