CN104603242A - 反乳化组合物和使用方法 - Google Patents
反乳化组合物和使用方法 Download PDFInfo
- Publication number
- CN104603242A CN104603242A CN201380043238.6A CN201380043238A CN104603242A CN 104603242 A CN104603242 A CN 104603242A CN 201380043238 A CN201380043238 A CN 201380043238A CN 104603242 A CN104603242 A CN 104603242A
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- Prior art keywords
- alcoxylates
- acid
- weight
- phenolic resin
- emulsion breaking
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 210
- 238000000034 method Methods 0.000 title claims abstract description 65
- 239000000839 emulsion Substances 0.000 claims abstract description 271
- 229920001568 phenolic resin Polymers 0.000 claims abstract description 117
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 41
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 41
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 41
- -1 alkyl phenolic resin Chemical compound 0.000 claims description 127
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 123
- 239000005011 phenolic resin Substances 0.000 claims description 116
- 229920005989 resin Polymers 0.000 claims description 99
- 239000011347 resin Substances 0.000 claims description 99
- 239000010779 crude oil Substances 0.000 claims description 78
- 229920000233 poly(alkylene oxides) Polymers 0.000 claims description 71
- 239000002253 acid Substances 0.000 claims description 66
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 60
- 239000003795 chemical substances by application Substances 0.000 claims description 55
- 239000003921 oil Substances 0.000 claims description 47
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 42
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 39
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 39
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 38
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 35
- 239000012071 phase Substances 0.000 claims description 35
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 31
- 239000008346 aqueous phase Substances 0.000 claims description 31
- 239000000126 substance Substances 0.000 claims description 29
- 235000013336 milk Nutrition 0.000 claims description 28
- 239000008267 milk Substances 0.000 claims description 28
- 210000004080 milk Anatomy 0.000 claims description 28
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 27
- 239000003208 petroleum Substances 0.000 claims description 27
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 21
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 21
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 21
- 239000006185 dispersion Substances 0.000 claims description 20
- 238000007046 ethoxylation reaction Methods 0.000 claims description 19
- 239000003495 polar organic solvent Substances 0.000 claims description 19
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 18
- 238000005260 corrosion Methods 0.000 claims description 18
- 230000007797 corrosion Effects 0.000 claims description 18
- 229920000642 polymer Polymers 0.000 claims description 18
- 239000003112 inhibitor Substances 0.000 claims description 17
- 125000003118 aryl group Chemical group 0.000 claims description 16
- HNRMPXKDFBEGFZ-UHFFFAOYSA-N ethyl trimethyl methane Natural products CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 claims description 16
- 239000000080 wetting agent Substances 0.000 claims description 16
- 239000003513 alkali Substances 0.000 claims description 15
- 239000003153 chemical reaction reagent Substances 0.000 claims description 15
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 14
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 14
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 14
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 14
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 14
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 claims description 14
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 13
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 claims description 12
- 229920001577 copolymer Polymers 0.000 claims description 12
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims description 10
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 9
- 235000011187 glycerol Nutrition 0.000 claims description 9
- MEIRRNXMZYDVDW-MQQKCMAXSA-N (2E,4E)-2,4-hexadien-1-ol Chemical compound C\C=C\C=C\CO MEIRRNXMZYDVDW-MQQKCMAXSA-N 0.000 claims description 8
- 239000001836 Dioctyl sodium sulphosuccinate Substances 0.000 claims description 8
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 8
- 150000008065 acid anhydrides Chemical class 0.000 claims description 8
- 150000001298 alcohols Chemical class 0.000 claims description 8
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 claims description 8
- 239000000693 micelle Substances 0.000 claims description 8
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 8
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 claims description 8
- RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical compound O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 claims description 8
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 7
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 7
- 239000002551 biofuel Substances 0.000 claims description 7
- 229920001400 block copolymer Polymers 0.000 claims description 7
- 229920006317 cationic polymer Polymers 0.000 claims description 7
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 claims description 7
- 239000001530 fumaric acid Substances 0.000 claims description 7
- 150000002632 lipids Chemical class 0.000 claims description 7
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 7
- 150000004702 methyl esters Chemical class 0.000 claims description 7
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 7
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims description 7
- 229920000768 polyamine Polymers 0.000 claims description 7
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 claims description 7
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 7
- 239000008096 xylene Substances 0.000 claims description 7
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 6
- COVZYZSDYWQREU-UHFFFAOYSA-N Busulfan Chemical compound CS(=O)(=O)OCCCCOS(C)(=O)=O COVZYZSDYWQREU-UHFFFAOYSA-N 0.000 claims description 6
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 6
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 6
- HUVYLRHAZAEUHY-UHFFFAOYSA-N 2-(4,5-dihydroimidazol-1-yl)ethanamine Chemical compound NCCN1CCN=C1 HUVYLRHAZAEUHY-UHFFFAOYSA-N 0.000 claims description 5
- GOHZKUSWWGUUNR-UHFFFAOYSA-N 2-(4,5-dihydroimidazol-1-yl)ethanol Chemical class OCCN1CCN=C1 GOHZKUSWWGUUNR-UHFFFAOYSA-N 0.000 claims description 5
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 description 26
- 238000012360 testing method Methods 0.000 description 26
- 230000015556 catabolic process Effects 0.000 description 24
- 235000013824 polyphenols Nutrition 0.000 description 23
- 239000013543 active substance Substances 0.000 description 20
- 238000005189 flocculation Methods 0.000 description 16
- 230000016615 flocculation Effects 0.000 description 16
- 239000000243 solution Substances 0.000 description 16
- 238000005406 washing Methods 0.000 description 16
- 238000009472 formulation Methods 0.000 description 14
- 239000000463 material Substances 0.000 description 14
- 238000006116 polymerization reaction Methods 0.000 description 14
- 239000003960 organic solvent Substances 0.000 description 12
- 229940014800 succinic anhydride Drugs 0.000 description 12
- 230000000694 effects Effects 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- 229920000371 poly(diallyldimethylammonium chloride) polymer Polymers 0.000 description 10
- 230000008569 process Effects 0.000 description 10
- 239000000523 sample Substances 0.000 description 10
- 229920001983 poloxamer Polymers 0.000 description 9
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 8
- YCLAMANSVUJYPT-UHFFFAOYSA-L aluminum chloride hydroxide hydrate Chemical compound O.[OH-].[Al+3].[Cl-] YCLAMANSVUJYPT-UHFFFAOYSA-L 0.000 description 8
- 230000005684 electric field Effects 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- 239000004094 surface-active agent Substances 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 7
- 239000003002 pH adjusting agent Substances 0.000 description 7
- 238000004062 sedimentation Methods 0.000 description 7
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- NSOXQYCFHDMMGV-UHFFFAOYSA-N Tetrakis(2-hydroxypropyl)ethylenediamine Chemical compound CC(O)CN(CC(C)O)CCN(CC(C)O)CC(C)O NSOXQYCFHDMMGV-UHFFFAOYSA-N 0.000 description 5
- 235000011054 acetic acid Nutrition 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 125000003158 alcohol group Chemical group 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical class OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 239000012266 salt solution Substances 0.000 description 5
- 239000003079 shale oil Substances 0.000 description 5
- FZGFBJMPSHGTRQ-UHFFFAOYSA-M trimethyl(2-prop-2-enoyloxyethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCOC(=O)C=C FZGFBJMPSHGTRQ-UHFFFAOYSA-M 0.000 description 5
- 238000011144 upstream manufacturing Methods 0.000 description 5
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 4
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 238000004088 simulation Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 230000002195 synergetic effect Effects 0.000 description 4
- 229920001864 tannin Polymers 0.000 description 4
- 239000001648 tannin Substances 0.000 description 4
- 235000018553 tannin Nutrition 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- NJSSICCENMLTKO-HRCBOCMUSA-N [(1r,2s,4r,5r)-3-hydroxy-4-(4-methylphenyl)sulfonyloxy-6,8-dioxabicyclo[3.2.1]octan-2-yl] 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)O[C@H]1C(O)[C@@H](OS(=O)(=O)C=2C=CC(C)=CC=2)[C@@H]2OC[C@H]1O2 NJSSICCENMLTKO-HRCBOCMUSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- LPTWEDZIPSKWDG-UHFFFAOYSA-N benzenesulfonic acid;dodecane Chemical compound OS(=O)(=O)C1=CC=CC=C1.CCCCCCCCCCCC LPTWEDZIPSKWDG-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 239000007822 coupling agent Substances 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 229940051250 hexylene glycol Drugs 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 239000007762 w/o emulsion Substances 0.000 description 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-UHFFFAOYSA-N 0.000 description 2
- OYINQIKIQCNQOX-UHFFFAOYSA-M 2-hydroxybutyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCC(O)C[N+](C)(C)C OYINQIKIQCNQOX-UHFFFAOYSA-M 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- ZMSBJRZDOBHDPU-UHFFFAOYSA-N C=O.NC(=O)N.C(CCC)C1=C(C=CC=C1)O Chemical compound C=O.NC(=O)N.C(CCC)C1=C(C=CC=C1)O ZMSBJRZDOBHDPU-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000002738 chelating agent Substances 0.000 description 2
- 238000001311 chemical methods and process Methods 0.000 description 2
- 238000005352 clarification Methods 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 2
- JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- DKAGJZJALZXOOV-UHFFFAOYSA-N hydrate;hydrochloride Chemical compound O.Cl DKAGJZJALZXOOV-UHFFFAOYSA-N 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- IHBKAGRPNRKYAO-UHFFFAOYSA-M methyl sulfate;trimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azanium Chemical compound COS([O-])(=O)=O.CC(=C)C(=O)OCC[N+](C)(C)C IHBKAGRPNRKYAO-UHFFFAOYSA-M 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 239000013049 sediment Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 125000000547 substituted alkyl group Chemical group 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- KQTIIICEAUMSDG-UHFFFAOYSA-N tricarballylic acid Chemical compound OC(=O)CC(C(O)=O)CC(O)=O KQTIIICEAUMSDG-UHFFFAOYSA-N 0.000 description 2
- RRHXZLALVWBDKH-UHFFFAOYSA-M trimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)OCC[N+](C)(C)C RRHXZLALVWBDKH-UHFFFAOYSA-M 0.000 description 2
- OEIXGLMQZVLOQX-UHFFFAOYSA-N trimethyl-[3-(prop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCCNC(=O)C=C OEIXGLMQZVLOQX-UHFFFAOYSA-N 0.000 description 2
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- 238000012935 Averaging Methods 0.000 description 1
- AMVPNVUYWCKGCO-UHFFFAOYSA-N C=CCCCCC.CC1=C(C(=O)O)C=CC=C1C(=O)O Chemical compound C=CCCCCC.CC1=C(C(=O)O)C=CC=C1C(=O)O AMVPNVUYWCKGCO-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 229960001040 ammonium chloride Drugs 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000002635 aromatic organic solvent Substances 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000011033 desalting Methods 0.000 description 1
- 125000005131 dialkylammonium group Chemical group 0.000 description 1
- IOMDIVZAGXCCAC-UHFFFAOYSA-M diethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](CC)(CC)CC=C IOMDIVZAGXCCAC-UHFFFAOYSA-M 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- HCPOCMMGKBZWSJ-UHFFFAOYSA-N ethyl 3-hydrazinyl-3-oxopropanoate Chemical compound CCOC(=O)CC(=O)NN HCPOCMMGKBZWSJ-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 description 1
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- BCHAIBIXCFCBIS-UHFFFAOYSA-N n'-(2-aminoethyl)ethane-1,2-diamine;oxirane Chemical compound C1CO1.NCCNCCN BCHAIBIXCFCBIS-UHFFFAOYSA-N 0.000 description 1
- ZUHZZVMEUAUWHY-UHFFFAOYSA-N n,n-dimethylpropan-1-amine Chemical compound CCCN(C)C ZUHZZVMEUAUWHY-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- IRUCBBFNLDIMIK-UHFFFAOYSA-N oct-4-ene Chemical compound CCCC=CCCC IRUCBBFNLDIMIK-UHFFFAOYSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 229940059574 pentaerithrityl Drugs 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 230000005501 phase interface Effects 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 229920005652 polyisobutylene succinic anhydride Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 150000003077 polyols Chemical group 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000001844 prenyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 125000005415 substituted alkoxy group Chemical group 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
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- 239000011592 zinc chloride Substances 0.000 description 1
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D17/00—Separation of liquids, not provided for elsewhere, e.g. by thermal diffusion
- B01D17/02—Separation of non-miscible liquids
- B01D17/04—Breaking emulsions
- B01D17/047—Breaking emulsions with separation aids
-
- 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
- C10G33/00—Dewatering or demulsification of hydrocarbon oils
- C10G33/04—Dewatering or demulsification of hydrocarbon oils with chemical means
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Materials Engineering (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Colloid Chemistry (AREA)
Abstract
Description
油相(总重量的90重量%) |
22.22重量%戊基酚醛树脂烷氧基化物 |
13.33重量%油溶性的EtO/PrO聚合物 |
53.33重量%石脑油和重芳族溶剂共混物 |
11.11重量%己二醇 |
实例2.1 | 重量% |
壬基酚醛树脂乙氧基化物(85%-90%EO) | 10 |
壬基酚醛树脂乙氧基化物(70%-80%EO) | 10 |
EO/PO嵌段共聚物(40%EO) | 5 |
EO/PO嵌段共聚物(80%EO) | 5 |
十二烷基苯磺酸 | 1 |
水 | 69 |
实例2.1A | 重量% |
壬基酚醛树脂乙氧基化物(85%-90%EO) | 10 |
壬基酚醛树脂乙氧基化物(70%-80%EO) | 10 |
EO/PO嵌段共聚物(40%EO) | 5 |
EO/PO嵌段共聚物(80%EO) | 5 |
十二烷基苯磺酸 | 1 |
柠檬酸 | 2 |
水 | 67 |
实例2.1B | 重量% |
壬基酚醛树脂乙氧基化物(85%-90%EO) | 13.5 |
壬基酚醛树脂乙氧基化物(70%-80%EO) | 6.5 |
EO/PO嵌段共聚物(40%EO) | 7 |
EO/PO嵌段共聚物(80%EO) | 3 |
十二烷基苯磺酸 | 1 |
柠檬酸 | 2 |
水 | 67 |
实例2.1C | 重量% |
壬基酚醛树脂乙氧基化物(85%-90%EO) | 15 |
壬基酚醛树脂乙氧基化物(70%-80%EO) | 5 |
EO/PO嵌段共聚物(40%EO) | 7 |
EO/PO嵌段共聚物(80%EO) | 3 |
十二烷基苯磺酸 | 1 |
柠檬酸 | 2 |
水 | 67 |
Claims (35)
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US201261682794P | 2012-08-14 | 2012-08-14 | |
US61/682794 | 2012-08-14 | ||
US13/627685 | 2012-09-26 | ||
US13/627,685 US9260601B2 (en) | 2012-09-26 | 2012-09-26 | Single drum oil and aqueous products and methods of use |
IN3955/DEL/2012 | 2012-12-21 | ||
IN3955DE2012 | 2012-12-21 | ||
PCT/US2013/052019 WO2014028193A1 (en) | 2012-08-14 | 2013-07-25 | Demulsifying compositions and methods of use |
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CN104603242A true CN104603242A (zh) | 2015-05-06 |
CN104603242B CN104603242B (zh) | 2017-03-08 |
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US (1) | US11629296B2 (zh) |
EP (1) | EP2885379B1 (zh) |
CN (1) | CN104603242B (zh) |
AU (1) | AU2013303110B2 (zh) |
CA (1) | CA2881292C (zh) |
MY (1) | MY171355A (zh) |
NZ (1) | NZ705155A (zh) |
PH (1) | PH12015500210A1 (zh) |
WO (1) | WO2014028193A1 (zh) |
Cited By (2)
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Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014123736A2 (en) * | 2013-02-07 | 2014-08-14 | General Electric Company | Compositions and methods for inhibiting fouling in hydrocarbons or petrochemicals |
JP5858115B1 (ja) * | 2014-09-03 | 2016-02-10 | 栗田工業株式会社 | o/w型エマルションの油水分離方法及びo/w型エマルション用油水分離剤 |
CA2978437C (en) * | 2015-03-04 | 2023-09-19 | Ecolab Usa Inc. | Reverse emulsion breaker polymers from poly(triethanolamine) |
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BR112018010928A2 (pt) | 2015-12-02 | 2018-12-04 | Ecolab Usa Inc | método de tratamento de uma corrente, e, líquido de desempenho multicomponente |
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US11926799B2 (en) | 2021-12-14 | 2024-03-12 | Saudi Arabian Oil Company | 2-iso-alkyl-2-(4-hydroxyphenyl)propane derivatives used as emulsion breakers for crude oil |
CN114891156B (zh) * | 2022-06-14 | 2022-12-06 | 南京理工大学 | 系列甲基烷基取代基二烯丙基氯化铵共聚物破乳剂及其制备方法 |
CN115521450B (zh) * | 2022-10-20 | 2024-05-28 | 德仕能源科技集团股份有限公司 | 聚合物及含有该聚合物的稠油冷采用降粘剂及其制备方法和应用 |
CN116162485A (zh) * | 2023-03-17 | 2023-05-26 | 中国石油化工股份有限公司 | 一种原油亲核解构助剂及其制备方法和应用 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101029252A (zh) * | 2007-03-23 | 2007-09-05 | 中国石油天然气股份有限公司 | 一种原油采出液脱水低温破乳剂 |
Family Cites Families (77)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1617739A (en) | 1925-11-21 | 1927-02-15 | Wm S Barnickel & Co | Process for breaking water-in-oil emulsions |
US2233383A (en) | 1940-03-06 | 1941-02-25 | Petrelite Corp Ltd | Composition of matter and a process for preventing water-in-oil type emulsions resulting from acidization of calcareous oil-bearing strata |
US2454545A (en) | 1944-09-09 | 1948-11-23 | Rohm & Haas | Hydrocarbon-substituted phenolformaldehyde condensates modified in the phenolic hydroxyl |
US2499365A (en) | 1947-03-07 | 1950-03-07 | Petrolite Corp | Chemical manufacture |
US2499370A (en) * | 1947-03-07 | 1950-03-07 | Petrolite Corp | Process for breaking petroleum emulsions |
US2615853A (en) | 1948-11-04 | 1952-10-28 | Visco Products Co | Method of breaking water-in-oil emulsions |
US2615653A (en) | 1949-02-03 | 1952-10-28 | Courtaulds Ltd | Creel |
US2754271A (en) | 1951-04-11 | 1956-07-10 | Visco Products Co | Method of breaking water-in-oil emulsions |
US2792353A (en) | 1953-04-20 | 1957-05-14 | Petrolite Corp | Process for breaking petroleum emulsions employing certain polyepoxidemodified oxyalkylated phenol-aldehyde resins |
US2888403A (en) | 1953-10-05 | 1959-05-26 | Petrolite Corp | Process for breaking emulsions employing lactone-derived compounds of certain oxyalkylated resins |
DE1271877B (de) * | 1963-04-23 | 1968-07-04 | Lubrizol Corp | Schmieroel |
US3499847A (en) | 1966-08-08 | 1970-03-10 | Petrolite Corp | Process for controlling the molecular weight of ultrahigh molecular weight oxyalkylene - containing polymers from alkylene oxides free of groups other than oxirane groups |
US3740421A (en) | 1966-09-19 | 1973-06-19 | Basf Wyandotte Corp | Polyoxyethylene-polyoxypropylene aqueous gels |
US3497006A (en) | 1967-12-26 | 1970-02-24 | Marathon Oil Co | High water content oil-external micellar dispersions |
US3506070A (en) | 1967-12-26 | 1970-04-14 | Marathon Oil Co | Use of water-external micellar dispersions in oil recovery |
US3708522A (en) | 1969-12-29 | 1973-01-02 | Lubrizol Corp | Reaction products of high molecular weight carboxylic acid esters and certain carboxylic acid acylating reactants |
US4032514A (en) | 1971-08-18 | 1977-06-28 | Petrolite Corporation | Oxyalkylated cyclic phenol-aldehyde resins and uses therefor |
US3928194A (en) | 1972-10-26 | 1975-12-23 | Texaco Inc | Emulsion breaking method |
US3977472A (en) | 1975-10-16 | 1976-08-31 | Exxon Production Research Company | Method of fracturing subterranean formations using oil-in-water emulsions |
US4058453A (en) | 1976-08-11 | 1977-11-15 | Texaco Exploration Canada Ltd. | Demulsification of oil emulsions with a mixture of polymers and alkaline earth metal halide |
US4446054A (en) | 1976-08-12 | 1984-05-01 | Petrolite Corporation | Demulsification of surfactant-petroleum-water flood emulsions |
US4209422A (en) | 1977-02-04 | 1980-06-24 | Exxon Research & Engineering Co. | Multicomponent demulsifier, method of using the same and hydrocarbon containing the same |
DE2719978C3 (de) * | 1977-05-04 | 1980-09-25 | Basf Ag, 6700 Ludwigshafen | Erdölemulsionsspalter |
US4326968A (en) | 1979-10-05 | 1982-04-27 | Magna Corporation | Method for breaking petroleum emulsions and the like using micellar solutions of thin film spreading agents comprising polyepoxide condensates of resinous polyalkylene oxide adducts and polyether polyols |
US4306981A (en) * | 1979-10-05 | 1981-12-22 | Magna Corporation | Method for breaking petroleum emulsions and the like comprising resinous polyalkylene oxide adducts |
US4342657A (en) | 1979-10-05 | 1982-08-03 | Magna Corporation | Method for breaking petroleum emulsions and the like using thin film spreading agents comprising a polyether polyol |
US4321147A (en) | 1980-05-22 | 1982-03-23 | Texaco Inc. | Demulsification of bitumen emulsions with a high molecular weight polyol containing discrete blocks of ethylene and propylene oxide |
US4321146A (en) | 1980-05-22 | 1982-03-23 | Texaco Inc. | Demulsification of bitumen emulsions with a high molecular weight mixed alkylene oxide polyol |
US4737265A (en) | 1983-12-06 | 1988-04-12 | Exxon Research & Engineering Co. | Water based demulsifier formulation and process for its use in dewatering and desalting crude hydrocarbon oils |
GB8527478D0 (en) * | 1985-11-07 | 1985-12-11 | Bp Chem Int Ltd | Demulsifiers |
DE3644385A1 (de) | 1986-12-24 | 1988-07-07 | Huels Chemische Werke Ag | Verfahren zur erhoehten gewinnung von erdoel aus einer unterirdischen lagerstaette durch tensidfluten |
US4800039A (en) | 1987-03-05 | 1989-01-24 | Calgon Corporation | Flocculation of suspended solids from aqueous solutions |
US4936867A (en) | 1987-04-24 | 1990-06-26 | Exxon Chemical Patents Inc. | Novel dispersants for oleaginous compositions |
US5032285A (en) | 1990-01-12 | 1991-07-16 | Nalco Chemical Company | Reverse emulsion breaking method using amine containing polymers |
US5080779A (en) | 1990-08-01 | 1992-01-14 | Betz Laboratories, Inc. | Methods for removing iron from crude oil in a two-stage desalting system |
IT1244498B (it) | 1991-02-20 | 1994-07-15 | Ecotec Srl | Procedimento per il trattamento disinquinante di soluzione acquose di soda caustica esauste da depurazione e lavaggio di prodotti petroliferi. |
US5120428A (en) | 1991-06-06 | 1992-06-09 | Energy Mines & Resources Canada | Deashing of heavy hydrocarbon residues |
CA2075749C (en) | 1991-08-12 | 2004-11-02 | William K. Stephenson | Desalting adjunct chemistry |
US5282959A (en) | 1992-03-16 | 1994-02-01 | Betz Laboratories, Inc. | Method for the extraction of iron from liquid hydrocarbons |
US5256305A (en) | 1992-08-24 | 1993-10-26 | Betz Laboratories, Inc. | Method for breaking emulsions in a crude oil desalting system |
CA2126889C (en) | 1993-09-02 | 2005-06-14 | Paul R. Hart | Method of breaking reverse emulsions in a crude oil desalting system |
SE512750C2 (sv) | 1993-11-29 | 2000-05-08 | Alfa Laval Separation Ab | Metod för gravimetrisk separation av olja som förorenats med partiklar och eller vatten |
US5449463A (en) | 1994-03-11 | 1995-09-12 | Nalco Chemical Company | Desalter wash water additive |
DE4418800A1 (de) | 1994-05-30 | 1995-12-07 | Basf Ag | Verfahren zur Abtrennung vom Wasser aus Rohöl und hierbei verwendete Erdölemulsionsspalter |
US5593572A (en) | 1994-08-04 | 1997-01-14 | Betzdearborn Inc. | Settling aids for solids in hydrocarbons |
US5611869A (en) | 1995-10-25 | 1997-03-18 | Betzdearborn Inc. | Refinery vessel cleaning treatment |
US5693257A (en) | 1995-12-06 | 1997-12-02 | Betzdearborn Inc. | Compositions and method for breaking water-in-oil emulsions |
CA2168392C (en) | 1996-01-30 | 2007-03-20 | Paul R. Hart | Settling aids for solids in hydrocarbons |
US5681451A (en) | 1996-01-31 | 1997-10-28 | Betzdearborn Inc. | Settling aids for solids in hydrocarbons |
US5773590A (en) | 1997-04-08 | 1998-06-30 | Betzdearborn Inc. | Methods of separating lignin solids and black liquor from tall oil fatty acids |
US5921912A (en) * | 1997-12-31 | 1999-07-13 | Betzdearborn Inc. | Copolmer formulations for breaking oil-and-water emulsions |
US6103100A (en) | 1998-07-01 | 2000-08-15 | Betzdearborn Inc. | Methods for inhibiting corrosion |
US6106701A (en) | 1998-08-25 | 2000-08-22 | Betzdearborn Inc. | Deasphalting process |
US6294093B1 (en) | 1998-09-04 | 2001-09-25 | Nalco/Exxon Energy Chemicals, L.P. | Aqueous dispersion of an oil soluble demulsifier for breaking crude oil emulsions |
US6228239B1 (en) | 1999-02-26 | 2001-05-08 | Exxon Research And Engineering Company | Crude oil desalting method |
ATE313612T1 (de) | 1999-11-30 | 2006-01-15 | Ici Plc | Verfahren zur behandlung von rohöl oder öl in einem raffinerieverfahren |
US8778322B2 (en) | 2001-10-18 | 2014-07-15 | Samyang Biopharmaceuticals Corporation | pH responsive biodegradable polylactic acid derivatives forming polymeric micelles and uses thereof for poorly water soluble drug delivery |
CN1205308C (zh) | 2002-01-10 | 2005-06-08 | 中国石油化工股份有限公司 | 用无机酸从烃油中脱除金属的方法 |
US6998382B2 (en) | 2002-02-28 | 2006-02-14 | Unilever Home & Personal Care Usa, A Division Of Conopco, Inc. | Process for making perfume containing surfactant compositions having perfume burst and enhanced perfume deposition when diluted |
US7048847B2 (en) * | 2003-02-03 | 2006-05-23 | General Electric Company | Settling aids for solids in hydrocarbons |
US20030173296A1 (en) | 2003-04-14 | 2003-09-18 | Costa Lawrence C | High recovery reverse osmosis process and apparatus |
US7160470B2 (en) | 2004-04-19 | 2007-01-09 | Davis Robert A | Method of clarifying industrial laundry wastewater using cationic dispersion polymers and anionic flocculent polymers |
US8197841B2 (en) | 2004-12-22 | 2012-06-12 | Bausch & Lomb Incorporated | Polymerizable surfactants and their use as device forming comonomers |
WO2006132160A1 (ja) | 2005-06-08 | 2006-12-14 | Tanah Process Ltd. | 液体のpH調整方法およびpH調整装置 |
US7612117B2 (en) | 2005-11-17 | 2009-11-03 | General Electric Company | Emulsion breaking process |
US7771588B2 (en) * | 2005-11-17 | 2010-08-10 | General Electric Company | Separatory and emulsion breaking processes |
US20090197978A1 (en) | 2008-01-31 | 2009-08-06 | Nimeshkumar Kantilal Patel | Methods for breaking crude oil and water emulsions |
MX2010009057A (es) | 2008-03-04 | 2010-09-09 | Basf Se | Uso de polialcanolaminas alcoxiladas para romper emulsiones de aceite-agua. |
US20100078331A1 (en) | 2008-10-01 | 2010-04-01 | Scherson Daniel A | ELECTROLYTIC DEVICE FOR GENERATION OF pH-CONTROLLED HYPOHALOUS ACID AQUEOUS SOLUTIONS FOR DISINFECTANT APPLICATIONS |
CN101734756A (zh) | 2008-11-20 | 2010-06-16 | 韩琳 | 一种自动调节反渗透产水ph系统 |
CN101463116B (zh) | 2009-01-12 | 2011-07-20 | 成都理工大学 | 非线型缔合水溶性四元共聚物及其制备方法和用途 |
CA2708870C (en) | 2009-08-05 | 2015-05-19 | Rohm And Haas Company | Polymers as additives for the separation of oil and water phases in emulsions and dispersions |
DE102009040495B4 (de) | 2009-09-08 | 2014-02-13 | Clariant International Ltd. | Alkoxylierte Thiacalixarene und deren Verwendung als Rohöl-Emulsionsspalter |
DE102009042971A1 (de) | 2009-09-24 | 2011-09-15 | Clariant International Ltd. | Alkoxylierte cyclische Diamine und deren Verwendung als Emulsionsspalter |
US8168062B2 (en) * | 2010-04-14 | 2012-05-01 | General Electric Company | Composition and method for breaking water in oil emulsions |
MX340805B (es) | 2011-04-18 | 2016-06-24 | Inst Mexicano Del Petróleo | Formulaciones sinergicas de copolimeros funcionalizados y liquidos ionicos para el deshidratado y desalado de aceites crudos medianos, pesados y extrapesados. |
US9260601B2 (en) * | 2012-09-26 | 2016-02-16 | General Electric Company | Single drum oil and aqueous products and methods of use |
-
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Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101029252A (zh) * | 2007-03-23 | 2007-09-05 | 中国石油天然气股份有限公司 | 一种原油采出液脱水低温破乳剂 |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110753741A (zh) * | 2017-06-19 | 2020-02-04 | Bp北美公司 | 除钙优化 |
US11242491B2 (en) | 2017-06-19 | 2022-02-08 | Bp Corporation North America Inc. | Calcium removal optimisation |
CN110753741B (zh) * | 2017-06-19 | 2022-07-15 | Bp北美公司 | 除钙优化 |
CN114456368A (zh) * | 2020-11-10 | 2022-05-10 | 中国石油化工股份有限公司 | 一种用于集输原油的减阻剂及其制备方法 |
CN114456368B (zh) * | 2020-11-10 | 2023-09-22 | 中国石油化工股份有限公司 | 一种用于集输原油的减阻剂及其制备方法 |
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US11629296B2 (en) | 2023-04-18 |
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CA2881292C (en) | 2021-01-12 |
WO2014028193A1 (en) | 2014-02-20 |
MY171355A (en) | 2019-10-10 |
EP2885379B1 (en) | 2018-02-14 |
CA2881292A1 (en) | 2014-02-20 |
AU2013303110A8 (en) | 2015-03-19 |
PH12015500210A1 (en) | 2015-03-16 |
US20150307788A1 (en) | 2015-10-29 |
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AU2013303110A1 (en) | 2015-03-05 |
AU2013303110B2 (en) | 2018-02-22 |
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