NO823593L - Fremgangsmaate til adskillelse av jordoljeemulsjoner av typen vann-i-olje. - Google Patents

Fremgangsmaate til adskillelse av jordoljeemulsjoner av typen vann-i-olje.

Info

Publication number: NO823593L
Authority: NO; Norway
Prior art keywords: weight; ethylene oxide; block polymer; oil; propylene oxide
Prior art date: 1981-10-29

Application number

NO823593A

Other languages

English (en)

Norwegian (no)

Inventor

Siegfried Billenstein

Hildegard Freundl

Ignaz Wimmer

Fritz Joachim Gohlke

Johannes Macenka

Original Assignee

Hoechst Ag

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.)

1981-10-29

Filing date

1982-10-28

Publication date

1983-05-02

1982-10-28 Application filed by Hoechst Ag filed Critical Hoechst Ag

1983-05-02 Publication of NO823593L publication Critical patent/NO823593L/no

Links

238000000034 method Methods 0.000 title claims description 11
229920000642 polymer Polymers 0.000 claims description 40
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 34
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 18
239000000839 emulsion Substances 0.000 claims description 16
238000006243 chemical reaction Methods 0.000 claims description 12
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
239000003208 petroleum Substances 0.000 claims description 12
150000001875 compounds Chemical class 0.000 claims description 11
RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 claims description 10
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 10
239000003377 acid catalyst Substances 0.000 claims description 7
239000007822 coupling agent Substances 0.000 claims description 5
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
239000003921 oil Substances 0.000 description 8
239000002904 solvent Substances 0.000 description 8
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 7
239000000243 solution Substances 0.000 description 7
239000008096 xylene Substances 0.000 description 7
229930040373 Paraformaldehyde Natural products 0.000 description 6
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 6
239000003054 catalyst Substances 0.000 description 6
229920002866 paraformaldehyde Polymers 0.000 description 6
239000010779 crude oil Substances 0.000 description 5
239000012467 final product Substances 0.000 description 5
239000003960 organic solvent Substances 0.000 description 5
229920001451 polypropylene glycol Polymers 0.000 description 5
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 4
239000007795 chemical reaction product Substances 0.000 description 4
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 4
239000000203 mixture Substances 0.000 description 4
239000000047 product Substances 0.000 description 4
238000003756 stirring Methods 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000007788 liquid Substances 0.000 description 3
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
-1 polyoxypropylene core Polymers 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
238000001816 cooling Methods 0.000 description 2
125000003827 glycol group Chemical group 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000006386 neutralization reaction Methods 0.000 description 2
238000000926 separation method Methods 0.000 description 2
230000007306 turnover Effects 0.000 description 2
BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 1
QLCJOAMJPCOIDI-UHFFFAOYSA-N 1-(butoxymethoxy)butane Chemical compound CCCCOCOCCCC QLCJOAMJPCOIDI-UHFFFAOYSA-N 0.000 description 1
IRTCJFCIQKNFPP-UHFFFAOYSA-N 2-methyl-1,4-dioxane Chemical compound CC1COCCO1 IRTCJFCIQKNFPP-UHFFFAOYSA-N 0.000 description 1
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
UXHQLGLGLZKHTC-CUNXSJBXSA-N 4-[(3s,3ar)-3-cyclopentyl-7-(4-hydroxypiperidine-1-carbonyl)-3,3a,4,5-tetrahydropyrazolo[3,4-f]quinolin-2-yl]-2-chlorobenzonitrile Chemical compound C1CC(O)CCN1C(=O)C1=CC=C(C=2[C@@H]([C@H](C3CCCC3)N(N=2)C=2C=C(Cl)C(C#N)=CC=2)CC2)C2=N1 UXHQLGLGLZKHTC-CUNXSJBXSA-N 0.000 description 1
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Natural products CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
201000004624 Dermatitis Diseases 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
239000003513 alkali Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
208000010668 atopic eczema Diseases 0.000 description 1
238000010533 azeotropic distillation Methods 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
ABDBNWQRPYOPDF-UHFFFAOYSA-N carbonofluoridic acid Chemical class OC(F)=O ABDBNWQRPYOPDF-UHFFFAOYSA-N 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
NKDDWNXOKDWJAK-UHFFFAOYSA-N dimethoxymethane Chemical compound COCOC NKDDWNXOKDWJAK-UHFFFAOYSA-N 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000001914 filtration Methods 0.000 description 1
UQSQSQZYBQSBJZ-UHFFFAOYSA-N fluorosulfonic acid Chemical class OS(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-N 0.000 description 1
239000006260 foam Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
238000005342 ion exchange Methods 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
YFSUTJLHUFNCNZ-UHFFFAOYSA-N perfluorooctane-1-sulfonic acid Chemical compound OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YFSUTJLHUFNCNZ-UHFFFAOYSA-N 0.000 description 1
SNGREZUHAYWORS-UHFFFAOYSA-N perfluorooctanoic acid Chemical compound OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F SNGREZUHAYWORS-UHFFFAOYSA-N 0.000 description 1
235000011007 phosphoric acid Nutrition 0.000 description 1
150000003016 phosphoric acids Chemical class 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000004753 textile Substances 0.000 description 1
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G4/00—Condensation polymers of aldehydes or ketones with polyalcohols; Addition polymers of heterocyclic oxygen compounds containing in the ring at least once the grouping —O—C—O—
- 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

Landscapes

Chemical & Material Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
General Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Polyethers (AREA)
Phenolic Resins Or Amino Resins (AREA)
Removal Of Floating Material (AREA)
Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

NO823593A 1981-10-29 1982-10-28 Fremgangsmaate til adskillelse av jordoljeemulsjoner av typen vann-i-olje. NO823593L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19813142954 DE3142954A1 (de)	1981-10-29	1981-10-29	"verfahren zum trennen von erdoelemulsionen vom typ wasser-in-oel"

Publications (1)

Publication Number	Publication Date
NO823593L true NO823593L (no)	1983-05-02

Family

ID=6145142

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO823593A NO823593L (no)	1981-10-29	1982-10-28	Fremgangsmaate til adskillelse av jordoljeemulsjoner av typen vann-i-olje.

Country Status (4)

Country	Link
EP (1)	EP0078489B1 (pt)
BR (1)	BR8206284A (pt)
DE (2)	DE3142954A1 (pt)
NO (1)	NO823593L (pt)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2609648B1 (fr) *	1987-01-16	1990-12-14	Total France	Agent desemulsifiant et antisalissure apte a separer des melanges eau-hydrocarbures, eventuellement mis en emulsion, et applications de cet agent

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1018179B (de) *	1956-04-07	1957-10-24	Hoechst Ag	Verfahren zum Entwaessern von Nassoelen
DE1495827A1 (de) *	1964-08-06	1969-06-12	Hoechst Ag	Verfahren zum Spalten von Emulsionen
DE2536121A1 (de) *	1974-08-19	1976-03-04	Basf Wyandotte Corp	Oberflaechenaktive block-polyoxyalkylencopolymere

1981
- 1981-10-29 DE DE19813142954 patent/DE3142954A1/de not_active Withdrawn
1982
- 1982-10-26 EP EP82109878A patent/EP0078489B1/de not_active Expired
- 1982-10-26 DE DE8282109878T patent/DE3267833D1/de not_active Expired
- 1982-10-27 BR BR8206284A patent/BR8206284A/pt unknown
- 1982-10-28 NO NO823593A patent/NO823593L/no unknown

Also Published As

Publication number	Publication date
BR8206284A (pt)	1983-09-20
DE3267833D1 (en)	1986-01-16
EP0078489A2 (de)	1983-05-11
EP0078489A3 (en)	1984-02-08
EP0078489B1 (de)	1985-12-04
DE3142954A1 (de)	1983-05-11

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US7671098B2 (en)	2010-03-02	Alkoxylated, cross-linked polyglycerols and use thereof as biodegradable demulsifier
US4420413A (en)	1983-12-13	Oxyalkylated addition products from ethylene oxide-propylene oxide block polymers and bis-glycidyl ethers and their use
US5039450A (en)	1991-08-13	Process for the separation of crude oil emulsions of the water-in-oil type
EP0097896B1 (de)	1986-10-15	Stickstoff enthaltende Erdöl-Emulsionsspalter und ihre Verwendung
US4465817A (en)	1984-08-14	Modified etherified phenol/aldehyde condensation products and their use for breaking petroleum emulsions
NO823593L (no)	1983-05-02	Fremgangsmaate til adskillelse av jordoljeemulsjoner av typen vann-i-olje.
US4705834A (en)	1987-11-10	Crosslinked oxyalkylated polyalkylenepolyamines
CN103052629A (zh)	2013-04-17	制备氨基三嗪烷氧基化物的方法
NO329347B1 (no)	2010-10-04	Anvendelse av alkoksylerte polyglyceroler som demulgeringsmidler
EP3092046B1 (de)	2018-04-18	Alkoxyliertes produkt und dessen verwendung
US1232620A (en)	1917-07-10	Tanning.
EP0246582A2 (de)	1987-11-25	Polyether, erhältlich durch Umsetzung von alkylolierten Bis-(4-hydroxyphenyl)-methanen mit Polyalkylenoxiden und deren Verwendung als Erdölemulsionsspalter
US2499361A (en)	1950-03-07	Oxyalkylated phenol-aldehyde diols
US2743253A (en)	1956-04-24	Oxyalkylated amine-modified thermoplastic phenol-aldehyde resins, and method of making same
RU2186088C1 (ru)	2002-07-27	Способ получения деэмульгатора
US2581367A (en)	1952-01-08	Oxyalkylated derivatives of certain solvent soluble phenol-aldehyde resins
US2864792A (en)	1958-12-16	Certain polyepoxide treated derivatives of monoepoxide-amine modified-resins, and method of making same
US2743251A (en)	1956-04-24	Oxyalkylated amine-modified thermoplastic phenol-aldehyde resins, and method of making same
US2864786A (en)	1958-12-16	Certain polyepoxide treated derivatives of monoepoxide-amine modified-resins, and method of making same
JPS6043164B2 (ja)	1985-09-26	原油乳濁液をを分理するための石油乳濁液分離剤
KR900014554A (ko)	1990-10-24	결합제. 이의 제조방법 및 경화성 혼합물에 있어서의 용도
DE2445873C3 (de)	1977-03-17	Verfahren zur Herstellung von verätherten Phenol-Aldehyd-Kondensationsprodukten und deren Verwendung zum Spalten von Rohölemulsionen
SU288713A1 (ru)		Способ разрушения нефтеводяной эмульсии
US2864794A (en)	1958-12-16	Aliphatic polyepoxide treated derivatives of alkylene oxide-amine modified phenolic resins, and method of making same