JP5890409B2 - 炭化水素から硫化水素を除去するためのアルファ−アミノエーテルの使用 - Google Patents
炭化水素から硫化水素を除去するためのアルファ−アミノエーテルの使用 Download PDFInfo
- Publication number
- JP5890409B2 JP5890409B2 JP2013519783A JP2013519783A JP5890409B2 JP 5890409 B2 JP5890409 B2 JP 5890409B2 JP 2013519783 A JP2013519783 A JP 2013519783A JP 2013519783 A JP2013519783 A JP 2013519783A JP 5890409 B2 JP5890409 B2 JP 5890409B2
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- Prior art keywords
- hydrogen sulfide
- alpha
- scavenger
- bis
- fluid
- 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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- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 title claims description 36
- 229910000037 hydrogen sulfide Inorganic materials 0.000 title claims description 32
- 229930195733 hydrocarbon Natural products 0.000 title claims description 19
- 150000002430 hydrocarbons Chemical class 0.000 title claims description 19
- 239000012530 fluid Substances 0.000 claims description 23
- 239000002516 radical scavenger Substances 0.000 claims description 20
- 239000004215 Carbon black (E152) Substances 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 10
- 239000007795 chemical reaction product Substances 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 3
- WUMYTJKLIVKYST-UHFFFAOYSA-N n-butyl-n-[(dibutylamino)methoxymethoxymethyl]butan-1-amine Chemical compound CCCCN(CCCC)COCOCN(CCCC)CCCC WUMYTJKLIVKYST-UHFFFAOYSA-N 0.000 claims description 3
- XHQHCZJKIMGMBY-UHFFFAOYSA-N n,n,n',n'-tetrabutylmethanediamine Chemical compound CCCCN(CCCC)CN(CCCC)CCCC XHQHCZJKIMGMBY-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 239000012808 vapor phase Substances 0.000 claims 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 21
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 16
- 150000001875 compounds Chemical class 0.000 description 11
- 238000009472 formulation Methods 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- 150000001299 aldehydes Chemical class 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 230000001172 regenerating effect Effects 0.000 description 4
- 230000002000 scavenging effect Effects 0.000 description 4
- 229940126062 Compound A Drugs 0.000 description 3
- 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 description 3
- -1 alkyl triazine Chemical compound 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 229930040373 Paraformaldehyde Natural products 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 239000010779 crude oil Substances 0.000 description 2
- 150000001923 cyclic compounds Chemical class 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- 229920002866 paraformaldehyde Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 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 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- OYWRDHBGMCXGFY-UHFFFAOYSA-N 1,2,3-triazinane Chemical compound C1CNNNC1 OYWRDHBGMCXGFY-UHFFFAOYSA-N 0.000 description 1
- BVOMRRWJQOJMPA-UHFFFAOYSA-N 1,2,3-trithiane Chemical compound C1CSSSC1 BVOMRRWJQOJMPA-UHFFFAOYSA-N 0.000 description 1
- LKLLNYWECKEQIB-UHFFFAOYSA-N 1,3,5-triazinane Chemical class C1NCNCN1 LKLLNYWECKEQIB-UHFFFAOYSA-N 0.000 description 1
- HUHGPYXAVBJSJV-UHFFFAOYSA-N 2-[3,5-bis(2-hydroxyethyl)-1,3,5-triazinan-1-yl]ethanol Chemical compound OCCN1CN(CCO)CN(CCO)C1 HUHGPYXAVBJSJV-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 150000001260 acyclic compounds Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000000116 mitigating effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- IVETVJOPRZJHDA-UHFFFAOYSA-N n-butyl-n-[(dibutylamino)methoxymethyl]butan-1-amine Chemical compound CCCCN(CCCC)COCN(CCCC)CCCC IVETVJOPRZJHDA-UHFFFAOYSA-N 0.000 description 1
- 231100001160 nonlethal Toxicity 0.000 description 1
- 239000010747 number 6 fuel oil Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
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- 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
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/148—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
- C07C7/152—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound by forming adducts or complexes
-
- 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
-
- 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
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/201—Impurities
- C10G2300/202—Heteroatoms content, i.e. S, N, O, P
-
- 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
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/201—Impurities
- C10G2300/207—Acid gases, e.g. H2S, COS, SO2, HCN
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Water Supply & Treatment (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Gas Separation By Absorption (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
「アルファ−アミノエーテル」という用語は、次式に従う分子を意味している:
Claims (1)
- 炭化水素流体中の硫化水素の量を、硫化水素捕捉剤を含む有効量の組成物と前記流体を接触させることによって、低下させる方法であって、前記硫化水素捕捉剤の量が、硫化水素と反応させて蒸気相の中に見出される硫化水素を低下させるのに十分な量であって、前記硫化水素捕捉剤と硫化水素との反応生成物が前記炭化水素流体中に可溶性で留まり、前記硫化水素捕捉剤が、N,N,N’,N’−テトラブチルメタンジアミン、N,N’−オキシビス(メチレン)ビス(N,N−ジブチレン)、及びN,N’−(メチレンビス(オキシ)ビス(メチレン))ビス(N,N’−ジブチルアミン)を含む、方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/836,037 | 2010-07-14 | ||
US12/836,037 US20120012507A1 (en) | 2010-07-14 | 2010-07-14 | Use of alpha-amino ethers for the removal of hydrogen sulfide from hydrocarbons |
PCT/US2011/043793 WO2012009396A2 (en) | 2010-07-14 | 2011-07-13 | Use of alpha-amino ethers for the removal of hydrogen sulfide from hydrocarbons |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2013531728A JP2013531728A (ja) | 2013-08-08 |
JP2013531728A5 JP2013531728A5 (ja) | 2014-08-28 |
JP5890409B2 true JP5890409B2 (ja) | 2016-03-22 |
Family
ID=45466088
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2013519783A Active JP5890409B2 (ja) | 2010-07-14 | 2011-07-13 | 炭化水素から硫化水素を除去するためのアルファ−アミノエーテルの使用 |
Country Status (12)
Country | Link |
---|---|
US (1) | US20120012507A1 (ja) |
EP (1) | EP2593535A4 (ja) |
JP (1) | JP5890409B2 (ja) |
KR (1) | KR20130047739A (ja) |
CN (1) | CN103403129B (ja) |
AR (1) | AR082165A1 (ja) |
BR (1) | BR112013000890A2 (ja) |
CA (1) | CA2805404C (ja) |
MX (1) | MX2013000507A (ja) |
RU (1) | RU2563633C2 (ja) |
SG (1) | SG187078A1 (ja) |
WO (1) | WO2012009396A2 (ja) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8663457B2 (en) * | 2011-11-23 | 2014-03-04 | General Electric Company | Methods and compounds for improving sulfide scavenging activity |
US9108899B2 (en) | 2011-12-30 | 2015-08-18 | General Electric Company | Sulfide scavengers, methods for making and methods for using |
US9278307B2 (en) | 2012-05-29 | 2016-03-08 | Baker Hughes Incorporated | Synergistic H2 S scavengers |
AU2013361683B2 (en) * | 2012-12-19 | 2018-06-14 | Nalco Company | Functionalized hydrogen sulfide scavengers |
WO2014100051A1 (en) | 2012-12-19 | 2014-06-26 | Nalco Company | Squeeze treatment for in situ scavenging of hydrogen sulfide |
CA2889615C (en) * | 2012-12-19 | 2021-03-02 | Nalco Company | Scavenging hydrogen sulfide |
BR112015015890A2 (pt) | 2013-01-30 | 2017-07-11 | Ecolab Usa Inc | sequestrantes de sulfeto de hidrogênio |
US9663390B2 (en) | 2013-05-10 | 2017-05-30 | Ecolab Usa Inc. | Reduction of hydrogen sulfide and/or malodor gassing from water via the addition of peroxyacetic acid/hydrogen peroxide product |
WO2014210166A1 (en) | 2013-06-27 | 2014-12-31 | Ecolab Usa Inc. | Epoxide-based hydrogen sulfide scavengers |
US9273254B2 (en) | 2013-12-20 | 2016-03-01 | Ecolab Usa Inc. | Amino acetals and ketals as hydrogen sulfide and mercaptan scavengers |
US9458393B2 (en) | 2014-04-15 | 2016-10-04 | Ecolab Usa Inc. | Hydantoins as hydrogen sulfide and mercaptan scavengers |
DK3286175T3 (da) | 2015-04-22 | 2021-01-04 | Ecolab Usa Inc | Udvikling af højtemperaturstabil scavenger til fjernelse af hydrogensulfid |
WO2017044248A1 (en) | 2015-09-08 | 2017-03-16 | Ecolab Usa Inc. | Hydrogen sulfide scavengers |
US10513662B2 (en) | 2017-02-02 | 2019-12-24 | Baker Hughes, A Ge Company, Llc | Functionalized aldehydes as H2S and mercaptan scavengers |
CN110573232A (zh) * | 2017-05-12 | 2019-12-13 | 株式会社可乐丽 | 含硫化合物去除装置和含硫化合物去除方法 |
WO2018218641A1 (en) * | 2017-06-02 | 2018-12-06 | General Electric Company | Method of mitigation of tramp amines in application of h2s scavengers |
CA3069435A1 (en) | 2017-07-13 | 2019-01-17 | Ecolab Usa Inc. | Method of removing a sulfur containing compound by adding a composition |
EP3914676A1 (en) | 2019-01-23 | 2021-12-01 | ChampionX USA Inc. | Complete removal of solids during hydrogen sulfide scavenging operations using a scavenger and a michael acceptor |
US20240110091A1 (en) | 2022-09-21 | 2024-04-04 | Championx Usa Inc. | Compositions and methods for scavenging sulfur-containing compounds |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4057403A (en) * | 1973-10-29 | 1977-11-08 | Fluor Corporation | Gas treating process |
US4405582A (en) * | 1982-01-18 | 1983-09-20 | Exxon Research And Engineering Co. | Process for selective removal of H2 S from mixtures containing H22 using diaminoether solutions |
US4556546A (en) * | 1983-05-04 | 1985-12-03 | Air Products And Chemicals, Inc. | Bis tertiary amino alkyl derivatives as solvents for acid gas removal from gas streams |
US4618481A (en) * | 1985-08-30 | 1986-10-21 | Exxon Research And Engineering Co. | Absorbent composition containing a severely hindered amino compound and an amine salt and process for the absorption of H2 S using the same |
CA2007965C (en) * | 1989-02-13 | 1996-02-27 | Jerry J. Weers | Suppression of the evolution of hydrogen sulfide gases from petroleum residua |
CA2017047C (en) * | 1989-08-01 | 1999-08-17 | Jerry J. Weers | Method of scavenging hydrogen sulfide from hydrocarbons |
CA2148849A1 (en) * | 1994-06-23 | 1995-12-24 | Kishan Bhatia | Method of treating sour gas and liquid hydrocarbons |
NO982505L (no) * | 1997-06-04 | 1998-12-07 | Nalco Exxon Energy Chem Lp | Sammensetning og fremgangsmÕte for avsvovling av gassformige eller flytende hydrokarboner, vandige systemer og blandinger derav |
CA2445422A1 (en) * | 2001-04-25 | 2002-10-31 | Clearwater International, Llc | Treatment of hydrocarbons containing sulfides |
CN101300223B (zh) * | 2005-08-09 | 2013-07-03 | 埃克森美孚研究工程公司 | 用于酸气涤气工艺的烷基氨基烷氧基(醇)单烷基醚 |
RU2349627C2 (ru) * | 2005-10-27 | 2009-03-20 | Ахматфаиль Магсумович Фахриев | Средство для удаления сероводорода и/или низкомолекулярных меркаптанов и способ его использования |
RU2499031C2 (ru) * | 2008-09-02 | 2013-11-20 | Дженерал Электрик Компани | Способ удаления сероводорода из сырой нефти |
US9394396B2 (en) * | 2011-06-21 | 2016-07-19 | Baker Hughes Incorporated | Hydrogen sulfide scavenger for use in hydrocarbons |
-
2010
- 2010-07-14 US US12/836,037 patent/US20120012507A1/en not_active Abandoned
-
2011
- 2011-07-13 JP JP2013519783A patent/JP5890409B2/ja active Active
- 2011-07-13 RU RU2013102414/04A patent/RU2563633C2/ru active
- 2011-07-13 BR BR112013000890A patent/BR112013000890A2/pt not_active Application Discontinuation
- 2011-07-13 SG SG2013002993A patent/SG187078A1/en unknown
- 2011-07-13 MX MX2013000507A patent/MX2013000507A/es active IP Right Grant
- 2011-07-13 CN CN201180034667.8A patent/CN103403129B/zh active Active
- 2011-07-13 KR KR1020137003671A patent/KR20130047739A/ko not_active Application Discontinuation
- 2011-07-13 EP EP20110807425 patent/EP2593535A4/en not_active Ceased
- 2011-07-13 WO PCT/US2011/043793 patent/WO2012009396A2/en active Application Filing
- 2011-07-13 AR ARP110102515A patent/AR082165A1/es active IP Right Grant
- 2011-07-13 CA CA2805404A patent/CA2805404C/en active Active
Also Published As
Publication number | Publication date |
---|---|
US20120012507A1 (en) | 2012-01-19 |
WO2012009396A3 (en) | 2012-05-18 |
RU2013102414A (ru) | 2014-08-20 |
EP2593535A4 (en) | 2014-04-23 |
CN103403129B (zh) | 2015-05-20 |
MX2013000507A (es) | 2013-02-27 |
EP2593535A2 (en) | 2013-05-22 |
SG187078A1 (en) | 2013-02-28 |
KR20130047739A (ko) | 2013-05-08 |
JP2013531728A (ja) | 2013-08-08 |
CA2805404C (en) | 2018-11-27 |
RU2563633C2 (ru) | 2015-09-20 |
AR082165A1 (es) | 2012-11-14 |
WO2012009396A2 (en) | 2012-01-19 |
CN103403129A (zh) | 2013-11-20 |
CA2805404A1 (en) | 2012-01-19 |
BR112013000890A2 (pt) | 2016-05-17 |
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