NO874722L - Forgrenede kvaternaere polyoksalkylenblandingspolyestere, fremgangsmaate til deres fremstilling og deres anvendelse. - Google Patents

Forgrenede kvaternaere polyoksalkylenblandingspolyestere, fremgangsmaate til deres fremstilling og deres anvendelse.

Info

Publication number: NO874722L
Authority: NO; Norway
Prior art keywords: acid; ethylene oxide; oxide units; polyoxalkylene; propylene oxide
Prior art date: 1986-11-13

Application number

NO874722A

Other languages

English (en)

Norwegian (no)

Other versions

NO874722D0 (no

Inventor

Willibald Boese

Manfred Hofinger

Martin Hille

Roland Boehm

Friedrich Staiss

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.)

1986-11-13

Filing date

1987-11-12

Publication date

1988-05-16

1987-11-12 Application filed by Hoechst Ag filed Critical Hoechst Ag

1987-11-12 Publication of NO874722D0 publication Critical patent/NO874722D0/no

1988-05-16 Publication of NO874722L publication Critical patent/NO874722L/no

Links

229920000728 polyester Polymers 0.000 title claims description 46
238000000034 method Methods 0.000 title description 6
238000002360 preparation method Methods 0.000 title description 5
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 65
239000000203 mixture Substances 0.000 claims description 60
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 39
150000001412 amines Chemical class 0.000 claims description 30
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 28
238000006243 chemical reaction Methods 0.000 claims description 28
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 27
238000005886 esterification reaction Methods 0.000 claims description 25
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 25
239000002253 acid Substances 0.000 claims description 22
229920000768 polyamine Polymers 0.000 claims description 22
239000007795 chemical reaction product Substances 0.000 claims description 21
230000032050 esterification Effects 0.000 claims description 21
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 18
239000000178 monomer Substances 0.000 claims description 18
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 16
239000010779 crude oil Substances 0.000 claims description 16
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 16
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 15
238000005260 corrosion Methods 0.000 claims description 13
230000007797 corrosion Effects 0.000 claims description 13
239000003054 catalyst Substances 0.000 claims description 12
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 12
150000008064 anhydrides Chemical class 0.000 claims description 11
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 10
125000004432 carbon atom Chemical group C* 0.000 claims description 9
239000001361 adipic acid Substances 0.000 claims description 8
235000011037 adipic acid Nutrition 0.000 claims description 8
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 8
229910052500 inorganic mineral Inorganic materials 0.000 claims description 8
239000011707 mineral Substances 0.000 claims description 8
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 8
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 7
239000003112 inhibitor Substances 0.000 claims description 7
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 7
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 6
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 6
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 6
239000004310 lactic acid Substances 0.000 claims description 6
235000014655 lactic acid Nutrition 0.000 claims description 6
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 5
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 5
235000011054 acetic acid Nutrition 0.000 claims description 5
150000001991 dicarboxylic acids Chemical class 0.000 claims description 5
239000000839 emulsion Substances 0.000 claims description 5
238000000605 extraction Methods 0.000 claims description 5
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 5
239000011976 maleic acid Substances 0.000 claims description 5
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 5
235000019260 propionic acid Nutrition 0.000 claims description 5
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 claims description 5
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 4
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 4
230000002378 acidificating effect Effects 0.000 claims description 4
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 4
WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 claims description 4
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims description 4
TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 claims description 4
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 4
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 claims description 3
125000001931 aliphatic group Chemical group 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 3
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 3
239000001530 fumaric acid Substances 0.000 claims description 3
238000006068 polycondensation reaction Methods 0.000 claims description 3
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 3
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 3
UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 claims description 2
239000004386 Erythritol Substances 0.000 claims description 2
239000004952 Polyamide Substances 0.000 claims description 2
150000007933 aliphatic carboxylic acids Chemical class 0.000 claims description 2
239000008346 aqueous phase Substances 0.000 claims description 2
UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 claims description 2
229940009714 erythritol Drugs 0.000 claims description 2
235000019414 erythritol Nutrition 0.000 claims description 2
WJSATVJYSKVUGV-UHFFFAOYSA-N hexane-1,3,5-triol Chemical compound CC(O)CC(O)CCO WJSATVJYSKVUGV-UHFFFAOYSA-N 0.000 claims description 2
CBCIHIVRDWLAME-UHFFFAOYSA-N hexanitrodiphenylamine Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1NC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O CBCIHIVRDWLAME-UHFFFAOYSA-N 0.000 claims description 2
239000000155 melt Substances 0.000 claims description 2
LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 claims description 2
229920002647 polyamide Polymers 0.000 claims description 2
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 claims description 2
125000003916 ethylene diamine group Chemical group 0.000 claims 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims 2
229910052799 carbon Inorganic materials 0.000 claims 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims 1
239000003345 natural gas Substances 0.000 claims 1
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 claims 1
238000005956 quaternization reaction Methods 0.000 description 37
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 14
239000000047 product Substances 0.000 description 13
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 11
239000007788 liquid Substances 0.000 description 11
230000035484 reaction time Effects 0.000 description 11
235000011007 phosphoric acid Nutrition 0.000 description 9
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 8
150000007513 acids Chemical class 0.000 description 8
150000001875 compounds Chemical class 0.000 description 8
-1 polypropylene Polymers 0.000 description 8
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical group OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
235000011167 hydrochloric acid Nutrition 0.000 description 6
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 5
239000002904 solvent Substances 0.000 description 5
238000003756 stirring Methods 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
230000000694 effects Effects 0.000 description 4
229940098779 methanesulfonic acid Drugs 0.000 description 4
239000012071 phase Substances 0.000 description 4
229920005862 polyol Polymers 0.000 description 4
238000000926 separation method Methods 0.000 description 4
239000003760 tallow Substances 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
239000003377 acid catalyst Substances 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
235000019197 fats Nutrition 0.000 description 3
229910052739 hydrogen Inorganic materials 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
TVZISJTYELEYPI-UHFFFAOYSA-N hypodiphosphoric acid Chemical compound OP(O)(=O)P(O)(O)=O TVZISJTYELEYPI-UHFFFAOYSA-N 0.000 description 3
230000005764 inhibitory process Effects 0.000 description 3
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
125000004433 nitrogen atom Chemical group N* 0.000 description 3
150000003016 phosphoric acids Chemical class 0.000 description 3
150000003077 polyols Chemical class 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
229920006395 saturated elastomer Polymers 0.000 description 3
239000000126 substance Substances 0.000 description 3
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
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235000013162 Cocos nucifera Nutrition 0.000 description 2
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CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 2
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DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
150000001450 anions Chemical class 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
238000009835 boiling Methods 0.000 description 2
239000001569 carbon dioxide Substances 0.000 description 2
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239000011261 inert gas Substances 0.000 description 2
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
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229910052757 nitrogen Inorganic materials 0.000 description 2
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
239000003921 oil Substances 0.000 description 2
ZFACJPAPCXRZMQ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O.OC(=O)C1=CC=CC=C1C(O)=O ZFACJPAPCXRZMQ-UHFFFAOYSA-N 0.000 description 2
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JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
150000003628 tricarboxylic acids Chemical class 0.000 description 1
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
238000005406 washing Methods 0.000 description 1
230000004580 weight loss Effects 0.000 description 1
238000009736 wetting Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
- C23F11/14—Nitrogen-containing compounds
- C23F11/145—Amides; N-substituted amides
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
- C08G63/685—Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen
- 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
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/54—Compositions for in situ inhibition of corrosion in boreholes or wells
- 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
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
- C23F11/14—Nitrogen-containing compounds
- C23F11/141—Amines; Quaternary ammonium compounds
- C23F11/143—Salts of amines
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
- C23F11/173—Macromolecular compounds

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Metallurgy (AREA)
Mechanical Engineering (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
General Life Sciences & Earth Sciences (AREA)
Polymers & Plastics (AREA)
Medicinal Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Polyesters Or Polycarbonates (AREA)
Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Detergent Compositions (AREA)

NO874722A 1986-11-13 1987-11-12 Forgrenede kvaternaere polyoksalkylenblandingspolyestere, fremgangsmaate til deres fremstilling og deres anvendelse. NO874722L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19863638744 DE3638744A1 (de)	1986-11-13	1986-11-13	Verzweigte, quaternaere polyoxalkylenmischpolyester, verfahren zu ihrer herstellung und ihre verwendung

Publications (2)

Publication Number	Publication Date
NO874722D0 NO874722D0 (no)	1987-11-12
NO874722L true NO874722L (no)	1988-05-16

Family

ID=6313845

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO874722A NO874722L (no)	1986-11-13	1987-11-12	Forgrenede kvaternaere polyoksalkylenblandingspolyestere, fremgangsmaate til deres fremstilling og deres anvendelse.

Country Status (6)

Country	Link
US (1)	US4885111A (fr)
EP (1)	EP0269887A3 (fr)
JP (1)	JPH01153721A (fr)
BR (1)	BR8706122A (fr)
DE (1)	DE3638744A1 (fr)
NO (1)	NO874722L (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4217985A1 (de) *	1992-05-30	1993-12-02	Hoechst Ag	Verfahren zum Trennen von Erdölemulsionen vom Wasser-in-Öl-Typ
JP2811433B2 (ja) *	1995-02-22	1998-10-15	三洋化成工業株式会社	帯電防止剤および樹脂組成物
AU2003212874A1 (en) *	2002-01-31	2003-09-02	Croda, Inc.	Additives and products including oligoesters
DE102005006030A1 (de) *	2005-02-09	2006-08-10	Basf Ag	Hyperverzweigte Polymere als Demulgatoren zum Spalten von Rohölemulsionen
EP2449153B1 (fr) *	2009-07-03	2019-01-09	Akzo Nobel Chemicals International B.V.	Inhibiteurs de corrosion polymérique
AU2011298474B2 (en)	2010-08-30	2014-01-16	Akzo Nobel Chemicals International B.V.	Use of polyester polyamine and polyester polyquaternary ammonium compounds as corrosion inhibitors
CA2822517A1 (fr) *	2010-12-28	2012-07-05	Akzo Nobel Chemicals International B.V.	Inhibiteurs de corrosion polyester-polyamine et polyester-poly(ammonium quaternaire)
EP3298102A1 (fr) *	2015-05-22	2018-03-28	Clariant International Ltd	Procédé pour le traitement acceptable sur le plan environnemental d'émulsions dans des opérations de récupération chimiquement assistée du pétrole
GB202102946D0 (en) *	2021-03-02	2021-04-14	Croda Int Plc	Quaternised polyol and polymer substrates containing the same

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3009884A (en) *	1957-07-29	1961-11-21	Petrolite Corp	Process for breaking emulsions of the oil-in-water class
DE3136298A1 (de) *	1981-09-12	1983-03-24	Hoechst Ag, 6000 Frankfurt	Quaternierte polymere polyoxyalkyl-alkylenpolyamine, verfahren zu deren herstellung und deren verwendung
AU2046583A (en) *	1982-11-19	1984-06-21	Dow Chemical Company, The	Quaternary amine salt of polyamine as demulsifier
DE3345156A1 (de) *	1983-12-14	1985-06-27	Hoechst Ag, 6230 Frankfurt	Quaternaere oxalkylierte polyester, verfahren zu deren herstellung und deren verwendung
DE3526600A1 (de) *	1985-07-25	1987-01-29	Hoechst Ag	Quaternaere oxalkylierte polykondensate, verfahren zu deren herstellung und deren verwendung

1986
- 1986-11-13 DE DE19863638744 patent/DE3638744A1/de not_active Withdrawn
1987
- 1987-11-03 EP EP87116125A patent/EP0269887A3/fr not_active Withdrawn
- 1987-11-12 NO NO874722A patent/NO874722L/no unknown
- 1987-11-12 JP JP62284405A patent/JPH01153721A/ja active Pending
- 1987-11-12 BR BR8706122A patent/BR8706122A/pt unknown
- 1987-11-12 US US07/119,823 patent/US4885111A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
JPH01153721A (ja)	1989-06-15
NO874722D0 (no)	1987-11-12
EP0269887A2 (fr)	1988-06-08
BR8706122A (pt)	1988-06-21
US4885111A (en)	1989-12-05
DE3638744A1 (de)	1988-05-26
EP0269887A3 (fr)	1989-06-28

Publication	Publication Date	Title
US8540885B2 (en)	2013-09-24	Use of alkoxylated polyalkanolamines for splitting oil-water emulsions
US4885110A (en)	1989-12-05	Branched polyoxyalkylene copolyesters, a process for their preparation, and their use
US4730079A (en)	1988-03-08	Quaternary oxalkylated polycondensates
US4536339A (en)	1985-08-20	Bisamides, a process for their preparation and their use
EP0086066B1 (fr)	1986-11-05	Utilisation de polyamidoamines ayant des groupes ammonium quaternaires comme désémulsifiants
NO874722L (no)	1988-05-16	Forgrenede kvaternaere polyoksalkylenblandingspolyestere, fremgangsmaate til deres fremstilling og deres anvendelse.
US9663705B2 (en)	2017-05-30	Method for resolving emulsions in enhanced oil recovery operations
US20240174797A1 (en)	2024-05-30	Polyesteramines and polyesterquats
RU2105788C1 (ru)	1998-02-27	Способ разделения нефтяных эмульсий типа вода-в-нефти
NO794170L (no)	1980-06-23	Emulsjonsbryter.
US4734523A (en)	1988-03-29	Oxalkylated polyester-amines, a process for their preparation and their use
CA2541296C (fr)	2013-11-26	Polymere d'alkylphenol-formaldehyde-diamine alcoxyle
CA1336843C (fr)	1995-08-29	Produits d'addition d'ether glycidylique esterifie et leur utilisation
US20050203193A1 (en)	2005-09-15	Demulsifiers
EP0092883B1 (fr)	1987-11-25	Procédé de désémulsification d'émulsions d'huile et d'eau avec des polyamidoamines d'ammonium hétérocycliques
US2324491A (en)	1943-07-20	Process for breaking petroleum emulsions
US5114616A (en)	1992-05-19	Esterified glycidyl ether addition products and their use
JPS5855463A (ja)	1983-04-01	ビスイミダゾリン、それらの製造方法およびそれらの用途
US4482724A (en)	1984-11-13	Bisimidazolines
EP3732219A1 (fr)	2020-11-04	Préparation d'agents de rupture d'émulsion de dessalage
US2723960A (en)	1955-11-15	Desalting compositions
US2366239A (en)	1945-01-02	Certain water-soluble high molal oxyalkylated esters, and method of making same
US2335489A (en)	1943-11-30	Certain water-soluble high molal oxyalkylated esters and method of making same
CN116806171A (zh)	2023-09-26	聚酯胺和聚酯季铵化合物
US2329699A (en)	1943-09-21	Process for breaking petroleum emulsions