JP2013542288A5 - - Google Patents
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- JP2013542288A5 JP2013542288A5 JP2013532270A JP2013532270A JP2013542288A5 JP 2013542288 A5 JP2013542288 A5 JP 2013542288A5 JP 2013532270 A JP2013532270 A JP 2013532270A JP 2013532270 A JP2013532270 A JP 2013532270A JP 2013542288 A5 JP2013542288 A5 JP 2013542288A5
- Authority
- JP
- Japan
- Prior art keywords
- anion
- mercury
- alkyl
- hydrocarbon fluid
- ionic liquid
- 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.)
- Granted
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- 238000000034 method Methods 0.000 claims description 104
- -1 transition metal cations Chemical class 0.000 claims description 83
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 75
- 229910052753 mercury Inorganic materials 0.000 claims description 73
- 150000001450 anions Chemical class 0.000 claims description 68
- 239000012530 fluid Substances 0.000 claims description 59
- 239000004215 Carbon black (E152) Substances 0.000 claims description 54
- 229930195733 hydrocarbon Natural products 0.000 claims description 54
- 150000002430 hydrocarbons Chemical class 0.000 claims description 54
- 239000002608 ionic liquid Substances 0.000 claims description 41
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 25
- 239000007787 solid Substances 0.000 claims description 25
- 239000000463 material Substances 0.000 claims description 21
- 125000000217 alkyl group Chemical group 0.000 claims description 19
- 239000000460 chlorine Substances 0.000 claims description 17
- 150000001768 cations Chemical class 0.000 claims description 14
- 229910052751 metal Inorganic materials 0.000 claims description 14
- 239000002184 metal Substances 0.000 claims description 14
- 150000003839 salts Chemical class 0.000 claims description 13
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 125000002091 cationic group Chemical group 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 125000001518 isoselenocyanato group Chemical group *N=C=[Se] 0.000 claims description 10
- 125000000129 anionic group Chemical group 0.000 claims description 9
- 239000012876 carrier material Substances 0.000 claims description 9
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 239000010949 copper Substances 0.000 claims description 8
- 230000003647 oxidation Effects 0.000 claims description 7
- 238000007254 oxidation reaction Methods 0.000 claims description 7
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims description 6
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 6
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
- 229910052723 transition metal Inorganic materials 0.000 claims description 6
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims description 6
- 229910021591 Copper(I) chloride Inorganic materials 0.000 claims description 5
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 claims description 5
- 239000003446 ligand Substances 0.000 claims description 5
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 150000004696 coordination complex Chemical class 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 239000007789 gas Substances 0.000 claims description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 4
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 4
- 229910052750 molybdenum Inorganic materials 0.000 claims description 4
- 239000011733 molybdenum Substances 0.000 claims description 4
- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- 239000010452 phosphate Substances 0.000 claims description 3
- 239000000377 silicon dioxide Substances 0.000 claims description 3
- SBYHFKPVCBCYGV-UHFFFAOYSA-O 1-azoniabicyclo[2.2.2]octane Chemical compound C1CC2CC[NH+]1CC2 SBYHFKPVCBCYGV-UHFFFAOYSA-O 0.000 claims description 2
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 claims description 2
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 claims description 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims description 2
- LJKVHZGQVDCXMY-UHFFFAOYSA-N 1H-borol-1-ium Chemical compound [BH2+]1C=CC=C1 LJKVHZGQVDCXMY-UHFFFAOYSA-N 0.000 claims description 2
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 claims description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-O 1H-indol-1-ium Chemical compound C1=CC=C2[NH2+]C=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-O 0.000 claims description 2
- DJMUYABFXCIYSC-UHFFFAOYSA-N 1H-phosphole Chemical compound C=1C=CPC=1 DJMUYABFXCIYSC-UHFFFAOYSA-N 0.000 claims description 2
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 claims description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- 229910014265 BrCl Inorganic materials 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 101710178035 Chorismate synthase 2 Proteins 0.000 claims description 2
- 229910021589 Copper(I) bromide Inorganic materials 0.000 claims description 2
- 101710152694 Cysteine synthase 2 Proteins 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 claims description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 2
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 claims description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-O Piperidinium(1+) Chemical compound C1CC[NH2+]CC1 NQRYJNQNLNOLGT-UHFFFAOYSA-O 0.000 claims description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims description 2
- WTKZEGDFNFYCGP-UHFFFAOYSA-O Pyrazolium Chemical compound C1=CN[NH+]=C1 WTKZEGDFNFYCGP-UHFFFAOYSA-O 0.000 claims description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 2
- RWRDLPDLKQPQOW-UHFFFAOYSA-O Pyrrolidinium ion Chemical compound C1CC[NH2+]C1 RWRDLPDLKQPQOW-UHFFFAOYSA-O 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-O Thiophenium Chemical compound [SH+]1C=CC=C1 YTPLMLYBLZKORZ-UHFFFAOYSA-O 0.000 claims description 2
- CYUBECYEVLLYPK-UHFFFAOYSA-N [O+]=1BC=CC=1 Chemical compound [O+]=1BC=CC=1 CYUBECYEVLLYPK-UHFFFAOYSA-N 0.000 claims description 2
- PTHKTFIRHVAWPY-UHFFFAOYSA-N [O+]=1PC=CC=1 Chemical compound [O+]=1PC=CC=1 PTHKTFIRHVAWPY-UHFFFAOYSA-N 0.000 claims description 2
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- CODNYICXDISAEA-UHFFFAOYSA-N bromine monochloride Chemical compound BrCl CODNYICXDISAEA-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 150000001721 carbon Chemical group 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- 239000010779 crude oil Substances 0.000 claims description 2
- NJDNXYGOVLYJHP-UHFFFAOYSA-L disodium;2-(3-oxido-6-oxoxanthen-9-yl)benzoate Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=CC(=O)C=C2OC2=CC([O-])=CC=C21 NJDNXYGOVLYJHP-UHFFFAOYSA-L 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 125000001153 fluoro group Chemical group F* 0.000 claims description 2
- 239000003502 gasoline Substances 0.000 claims description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-O guanidinium Chemical compound NC(N)=[NH2+] ZRALSGWEFCBTJO-UHFFFAOYSA-O 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-O hydron piperazine Chemical compound [H+].C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-O 0.000 claims description 2
- ZCQWOFVYLHDMMC-UHFFFAOYSA-O hydron;1,3-oxazole Chemical compound C1=COC=[NH+]1 ZCQWOFVYLHDMMC-UHFFFAOYSA-O 0.000 claims description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-O hydron;quinoline Chemical compound [NH+]1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-O 0.000 claims description 2
- LPAGFVYQRIESJQ-UHFFFAOYSA-N indoline Chemical compound C1=CC=C2NCCC2=C1 LPAGFVYQRIESJQ-UHFFFAOYSA-N 0.000 claims description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- AWJUIBRHMBBTKR-UHFFFAOYSA-O isoquinolin-2-ium Chemical compound C1=[NH+]C=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-O 0.000 claims description 2
- 239000003350 kerosene Substances 0.000 claims description 2
- 239000003949 liquefied natural gas Substances 0.000 claims description 2
- 239000003915 liquefied petroleum gas Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 229910021645 metal ion Inorganic materials 0.000 claims description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-O morpholinium Chemical compound [H+].C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-O 0.000 claims description 2
- 239000003345 natural gas Substances 0.000 claims description 2
- 239000003498 natural gas condensate Substances 0.000 claims description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 claims description 2
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 claims description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 claims description 2
- WVIICGIFSIBFOG-UHFFFAOYSA-N pyrylium Chemical compound C1=CC=[O+]C=C1 WVIICGIFSIBFOG-UHFFFAOYSA-N 0.000 claims description 2
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 claims description 2
- XSCHRSMBECNVNS-UHFFFAOYSA-O quinoxalin-1-ium Chemical compound [NH+]1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-O 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims description 2
- 125000003831 tetrazolyl group Chemical group 0.000 claims description 2
- 125000001425 triazolyl group Chemical group 0.000 claims description 2
- 125000005500 uronium group Chemical group 0.000 claims description 2
- 210000002845 virion Anatomy 0.000 claims description 2
- 239000012991 xanthate Substances 0.000 claims description 2
- FTTATHOUSOIFOQ-UHFFFAOYSA-N 1,2,3,4,6,7,8,8a-octahydropyrrolo[1,2-a]pyrazine Chemical compound C1NCCN2CCCC21 FTTATHOUSOIFOQ-UHFFFAOYSA-N 0.000 claims 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 229910052796 boron Inorganic materials 0.000 claims 1
- 229910052802 copper Inorganic materials 0.000 claims 1
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims 1
- URSLCTBXQMKCFE-UHFFFAOYSA-N dihydrogenborate Chemical compound OB(O)[O-] URSLCTBXQMKCFE-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 101100293720 Caenorhabditis elegans ncs-2 gene Proteins 0.000 description 1
- VMQMZMRVKUZKQL-UHFFFAOYSA-N Cu+ Chemical compound [Cu+] VMQMZMRVKUZKQL-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-L Malonate Chemical compound [O-]C(=O)CC([O-])=O OFOBLEOULBTSOW-UHFFFAOYSA-L 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 239000013626 chemical specie Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- JBFYUZGYRGXSFL-UHFFFAOYSA-N imidazolide Chemical compound C1=C[N-]C=N1 JBFYUZGYRGXSFL-UHFFFAOYSA-N 0.000 description 1
- 229910001411 inorganic cation Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- LGRLWUINFJPLSH-UHFFFAOYSA-N methanide Chemical compound [CH3-] LGRLWUINFJPLSH-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1016751.8 | 2010-10-05 | ||
| GB1016751.8A GB2484301B8 (en) | 2010-10-05 | 2010-10-05 | Process for removing metals from hydrocarbons |
| PCT/GB2011/051906 WO2012046057A2 (en) | 2010-10-05 | 2011-10-05 | Process for removing metals from hydrocarbons |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016083361A Division JP6231606B2 (ja) | 2010-10-05 | 2016-04-19 | 炭化水素から金属を除去するためのプロセス |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013542288A JP2013542288A (ja) | 2013-11-21 |
| JP2013542288A5 true JP2013542288A5 (enExample) | 2014-11-20 |
| JP5925786B2 JP5925786B2 (ja) | 2016-05-25 |
Family
ID=43243537
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013532270A Active JP5925786B2 (ja) | 2010-10-05 | 2011-10-05 | 炭化水素から金属を除去するためのプロセス |
| JP2016083361A Active JP6231606B2 (ja) | 2010-10-05 | 2016-04-19 | 炭化水素から金属を除去するためのプロセス |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016083361A Active JP6231606B2 (ja) | 2010-10-05 | 2016-04-19 | 炭化水素から金属を除去するためのプロセス |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US9447335B2 (enExample) |
| EP (2) | EP3095841B1 (enExample) |
| JP (2) | JP5925786B2 (enExample) |
| CN (2) | CN106350098B (enExample) |
| AU (2) | AU2011311317B2 (enExample) |
| BR (1) | BR112013008411B1 (enExample) |
| CA (2) | CA2813490C (enExample) |
| EA (2) | EA035774B1 (enExample) |
| GB (2) | GB2547364B8 (enExample) |
| MY (1) | MY164886A (enExample) |
| NZ (1) | NZ609179A (enExample) |
| SG (1) | SG189303A1 (enExample) |
| WO (1) | WO2012046057A2 (enExample) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0905896D0 (en) * | 2009-04-06 | 2009-05-20 | Univ Belfast | Process for removing metals from hydrocarbons |
| GB0905894D0 (en) * | 2009-04-06 | 2009-05-20 | Univ Belfast | Ionic liquids solvents for metals and metal compounds |
| GB2547364B8 (en) * | 2010-10-05 | 2017-11-29 | The Queen's Univ Of Belfast | Process for removing metals from hydrocarbons |
| GB2485824B (en) * | 2010-11-25 | 2017-12-20 | The Queen's Univ Of Belfast | Process for removing organic acids from crude oil and crude oil distillates |
| DE202011106025U1 (de) | 2011-08-14 | 2012-08-17 | BLüCHER GMBH | Aktivkohle mit metallbasierter Komponente |
| DE202011106028U1 (de) * | 2011-08-14 | 2012-08-17 | BLüCHER GMBH | Neue Konzepte für die Gasbehandlung und Gasreinigung |
| PE20160226A1 (es) * | 2013-03-14 | 2016-05-11 | Conocophillips Co | Eliminacion del mercurio del petroleo crudo |
| US9574140B2 (en) | 2013-03-14 | 2017-02-21 | Conocophillips Company | Removing mercury from crude oil |
| DE102013104696A1 (de) * | 2013-05-07 | 2014-11-13 | L'Air Liquide, Société Anonyme pour l'Etude et l'Exploitation des Procédés Georges Claude | Verfahren zur Entfernung von Metallen aus hochsiedenden Kohlenwasserstofffraktionen |
| WO2015077746A2 (en) * | 2013-11-25 | 2015-05-28 | Milliken & Company | Filtration medium and process for filtering a fluid stream |
| MY175927A (en) * | 2015-03-03 | 2020-07-15 | Petroliam Nasional Berhad Petronas | Process for removing heavy metals from hydrocarbons |
| WO2016148735A1 (en) | 2015-03-16 | 2016-09-22 | University Of Wyoming | Methods and compositions for the removal of mercury from gases |
| WO2018104257A1 (en) | 2016-12-05 | 2018-06-14 | Umicore | Removal of arsenic from flue-gas |
| GB2560871B (en) * | 2016-12-16 | 2020-06-03 | Univ Belfast | Separation of rare earth matals |
| CN107141312B (zh) * | 2017-06-28 | 2019-08-13 | 北京理工大学 | 一种四唑氰基硼酸离子液体及其制备方法 |
| US10633600B2 (en) * | 2017-08-15 | 2020-04-28 | Conocophillips Company | Process for removing mercury from crude oil |
| US11499101B2 (en) | 2017-11-28 | 2022-11-15 | Khalifa University of Science and Technology | Mercury capture from hydrocarbon fluids using deep eutectic solvents |
| WO2019113513A1 (en) | 2017-12-08 | 2019-06-13 | Baker Hughes, A Ge Company, Llc | Ionic liquid based well asphaltene inhibitors and methods of using the same |
| EA202091413A1 (ru) | 2018-07-11 | 2020-09-24 | Бейкер Хьюз Холдингз Ллк | Скважинные ингибиторы асфальтенов на основе ионной жидкости и способы их применения |
| CN109621640B (zh) * | 2018-12-28 | 2021-02-26 | 河北科技大学 | 一种用于吸收so2的负载型离子液体变色材料及其制备方法和应用 |
| CN109758897A (zh) * | 2019-02-01 | 2019-05-17 | 四川大学 | 一种湿法脱硫工艺中脱除汞污染物方法 |
| AU2020350589A1 (en) * | 2019-09-16 | 2022-03-24 | Albemarle Corporation | Processes for reducing environmental availability of environmental pollutants |
| CN113046176A (zh) * | 2019-12-27 | 2021-06-29 | 丰益(上海)生物技术研发中心有限公司 | 去除流体物料中塑化剂的方法 |
| US11168265B2 (en) | 2020-01-14 | 2021-11-09 | Baker Hughes Oilfield Operations Llc | Process of removing metal contaminants from light hydrocarbons |
| EP4149671A1 (en) * | 2020-05-12 | 2023-03-22 | W. L. Gore & Associates, Inc. | Sorbent polymer composites including phophonium halides, flue gas treatment devices and flue gas treatment methods utilizing the same |
| CN114539056B (zh) * | 2020-11-24 | 2023-03-14 | 中国科学院大连化学物理研究所 | 一种甲醇羰基化制备乙酸甲酯的方法 |
| CN114534780B (zh) * | 2020-11-24 | 2023-06-13 | 中国科学院大连化学物理研究所 | 一种负载型的硫鎓锚定单原子催化剂及制备方法 |
| CN115710647B (zh) * | 2021-08-23 | 2023-10-20 | 北京大学 | 一种利用离子液体体系从含裂变元素的硝酸溶液中萃取分离钼的方法 |
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| WO2024252360A1 (en) * | 2023-06-07 | 2024-12-12 | Petroliam Nasional Berhad (Petronas) | Mercury removal from produced water feeds |
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