NO874723L - Forgrende polyoksalkylenblandingspolyestere, fremgangsmaate til deres fremstilling og deres anvendelse. - Google Patents

Forgrende polyoksalkylenblandingspolyestere, fremgangsmaate til deres fremstilling og deres anvendelse.

Info

Publication number: NO874723L
Authority: NO; Norway
Prior art keywords: acid; oxide units; polyamine; dicarboxylic; ethylene oxide
Prior art date: 1986-11-13

Application number

NO874723A

Other languages

English (en)

Norwegian (no)

Other versions

NO874723D0 (no

Inventor

Willibald Boese

Manfred Hofinger

Martin Hille

Ronald 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 NO874723D0 publication Critical patent/NO874723D0/no

1988-05-16 Publication of NO874723L publication Critical patent/NO874723L/no

Links

229920000728 polyester Polymers 0.000 title claims description 29
238000000034 method Methods 0.000 title description 5
238000002360 preparation method Methods 0.000 title description 4
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 41
239000000203 mixture Substances 0.000 claims description 37
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 32
150000001412 amines Chemical class 0.000 claims description 32
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 27
238000006243 chemical reaction Methods 0.000 claims description 27
229920000768 polyamine Polymers 0.000 claims description 26
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 23
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 20
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
239000010779 crude oil Substances 0.000 claims description 17
239000003054 catalyst Substances 0.000 claims description 14
150000008064 anhydrides Chemical class 0.000 claims description 13
150000001991 dicarboxylic acids Chemical class 0.000 claims description 11
239000000839 emulsion Substances 0.000 claims description 11
239000001361 adipic acid Substances 0.000 claims description 10
235000011037 adipic acid Nutrition 0.000 claims description 10
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 10
238000005886 esterification reaction Methods 0.000 claims description 9
239000002253 acid 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-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 7
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 6
230000032050 esterification Effects 0.000 claims description 6
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 5
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 5
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 5
125000004432 carbon atom Chemical group C* 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
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 5
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-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
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 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
238000006068 polycondensation reaction Methods 0.000 claims description 4
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 4
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 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
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 3
239000004386 Erythritol Substances 0.000 claims description 2
UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 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
239000001530 fumaric acid Substances 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
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
150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
150000001735 carboxylic acids Chemical class 0.000 claims 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 11
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 8
150000001875 compounds Chemical class 0.000 description 7
235000019197 fats Nutrition 0.000 description 7
230000035484 reaction time Effects 0.000 description 7
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
239000007795 chemical reaction product Substances 0.000 description 6
235000011167 hydrochloric acid Nutrition 0.000 description 6
150000003839 salts Chemical class 0.000 description 6
239000003760 tallow Substances 0.000 description 6
230000000694 effects Effects 0.000 description 5
-1 polypropylene Polymers 0.000 description 5
238000000926 separation method Methods 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
TVZISJTYELEYPI-UHFFFAOYSA-N hypodiphosphoric acid Chemical compound OP(O)(=O)P(O)(O)=O TVZISJTYELEYPI-UHFFFAOYSA-N 0.000 description 4
229940098779 methanesulfonic acid Drugs 0.000 description 4
239000003921 oil Substances 0.000 description 4
235000011007 phosphoric acid Nutrition 0.000 description 4
239000002904 solvent Substances 0.000 description 4
235000013162 Cocos nucifera Nutrition 0.000 description 3
244000060011 Cocos nucifera Species 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-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
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
229920005862 polyol Polymers 0.000 description 3
150000003077 polyols Chemical class 0.000 description 3
239000000047 product Substances 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
229920006395 saturated elastomer Polymers 0.000 description 3
238000003756 stirring Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
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
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-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
239000003377 acid catalyst Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
238000000605 extraction Methods 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
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
239000007788 liquid Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
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
ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 2
150000003016 phosphoric acids Chemical class 0.000 description 2
239000002689 soil Substances 0.000 description 2
230000007306 turnover Effects 0.000 description 2
239000008096 xylene Substances 0.000 description 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-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
QISOBCMNUJQOJU-UHFFFAOYSA-N 4-bromo-1h-pyrazole-5-carboxylic acid Chemical compound OC(=O)C=1NN=CC=1Br QISOBCMNUJQOJU-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
235000014820 Galium aparine Nutrition 0.000 description 1
240000005702 Galium aparine Species 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
235000011054 acetic acid Nutrition 0.000 description 1
230000001154 acute effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
235000020661 alpha-linolenic acid Nutrition 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
238000010533 azeotropic distillation Methods 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000001110 calcium chloride Substances 0.000 description 1
229910001628 calcium chloride Inorganic materials 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000000571 coke Substances 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
HEBKCHPVOIAQTA-NGQZWQHPSA-N d-xylitol Chemical compound OC[C@H](O)C(O)[C@H](O)CO HEBKCHPVOIAQTA-NGQZWQHPSA-N 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
238000009826 distribution Methods 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000013505 freshwater Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
125000001183 hydrocarbyl group Chemical group 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
235000020778 linoleic acid Nutrition 0.000 description 1
OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
229960004488 linolenic acid Drugs 0.000 description 1
KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
229910001629 magnesium chloride Inorganic materials 0.000 description 1
HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
150000002889 oleic acids Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
YTSACTNRGUJEGO-UHFFFAOYSA-N oxirane prop-1-ene Chemical group CC=C.C1CO1 YTSACTNRGUJEGO-UHFFFAOYSA-N 0.000 description 1
150000004965 peroxy acids Chemical class 0.000 description 1
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 1
229920001281 polyalkylene Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
238000000859 sublimation Methods 0.000 description 1
230000008022 sublimation Effects 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
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
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
239000007762 w/o emulsion Substances 0.000 description 1
238000005406 washing Methods 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
- 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
- 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)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Oil, Petroleum & Natural Gas (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Engineering & Computer Science (AREA)
General Chemical & Material Sciences (AREA)
Polyesters Or Polycarbonates (AREA)
Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

NO874723A 1986-11-13 1987-11-12 Forgrende polyoksalkylenblandingspolyestere, fremgangsmaate til deres fremstilling og deres anvendelse. NO874723L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19863638743 DE3638743A1 (de)	1986-11-13	1986-11-13	Verzweigte polyoxalkylenmischpolyester, verfahren zu ihrer herstellung und ihre verwendung

Publications (2)

Publication Number	Publication Date
NO874723D0 NO874723D0 (no)	1987-11-12
NO874723L true NO874723L (no)	1988-05-16

Family

ID=6313844

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO874723A NO874723L (no)	1986-11-13	1987-11-12	Forgrende polyoksalkylenblandingspolyestere, fremgangsmaate til deres fremstilling og deres anvendelse.

Country Status (6)

Country	Link
US (1)	US4885110A (fr)
EP (1)	EP0267517A3 (fr)
JP (1)	JPS63135422A (fr)
BR (1)	BR8706127A (fr)
DE (1)	DE3638743A1 (fr)
NO (1)	NO874723L (fr)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8806419D0 (en) *	1988-03-18	1988-04-20	Du Pont	Improvements relating to fibres
US5085699A (en) *	1991-04-08	1992-02-04	Westvaco Corporation	Amniopolyester resins as dilution extenders for zinc-containing metal resinate inks
DE4217985A1 (de) *	1992-05-30	1993-12-02	Hoechst Ag	Verfahren zum Trennen von Erdölemulsionen vom Wasser-in-Öl-Typ
EP0584708B1 (fr) *	1992-08-22	1998-05-13	Clariant GmbH	Désémulsifiants polyfonctionnels pour huiles brutes
US5510452A (en) *	1994-07-11	1996-04-23	Rheox, Inc.	Pourable liquid polyesteramide rheological additives and the use thererof
DE19643832A1 (de) *	1996-10-30	1998-05-07	Clariant Gmbh	Schwere Öle mit verbesserten Eigenschaften und ein Additiv dafür
GB0228192D0 (en) *	2002-12-03	2003-01-08	Dynea Asa	Demulsifiers for crude oil emulsions
DE102005006030A1 (de) *	2005-02-09	2006-08-10	Basf Ag	Hyperverzweigte Polymere als Demulgatoren zum Spalten von Rohölemulsionen
DE102005006317A1 (de) *	2005-02-11	2006-08-24	Clariant Produkte (Deutschland) Gmbh	Polyetheramin-Makromonomere mit zwei benachbarten primären Hydroxylgruppen und ihre Verwendung zur Herstellung von Polyurethanen
WO2007039083A1 (fr) *	2005-09-20	2007-04-12	Dsm Ip Assets B.V.	Procede de rupture d’emulsions ou de prevention de la formation d’emulsions
WO2009047210A1 (fr)	2007-10-08	2009-04-16	Basf Se	Utilisation de polyesters et/ou de polyesters amides hyperramifiés pour séparer des émulsions huile dans l'eau
WO2010076253A1 (fr)	2008-12-29	2010-07-08	Basf Se	Polyesters et polycarbonates hyperramifiés servant de désémulsifiants pour le craquage d'émulsions de pétrole brut
US20170189832A1 (en)	2014-05-28	2017-07-06	Basf Se	Coated mesh and its use for oil-water separation
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DE3345156A1 (de) *	1983-12-14	1985-06-27	Hoechst Ag, 6230 Frankfurt	Quaternaere oxalkylierte polyester, verfahren zu deren herstellung und deren verwendung
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1986
- 1986-11-13 DE DE19863638743 patent/DE3638743A1/de not_active Withdrawn
1987
- 1987-11-03 EP EP87116124A patent/EP0267517A3/fr not_active Withdrawn
- 1987-11-12 NO NO874723A patent/NO874723L/no unknown
- 1987-11-12 US US07/119,817 patent/US4885110A/en not_active Expired - Fee Related
- 1987-11-12 JP JP62284404A patent/JPS63135422A/ja active Pending
- 1987-11-12 BR BR8706127A patent/BR8706127A/pt unknown

Also Published As

Publication number	Publication date
JPS63135422A (ja)	1988-06-07
EP0267517A2 (fr)	1988-05-18
BR8706127A (pt)	1988-06-21
NO874723D0 (no)	1987-11-12
DE3638743A1 (de)	1988-05-26
US4885110A (en)	1989-12-05
EP0267517A3 (fr)	1989-06-14

Publication	Publication Date	Title
NO874723L (no)	1988-05-16	Forgrende polyoksalkylenblandingspolyestere, fremgangsmaate til deres fremstilling og deres anvendelse.
US2562878A (en)	1951-08-07	Processes for breaking emulsions
NO313036B1 (no)	2002-08-05	Demulgeringsmiddel for vann-i-olje-emulsjoner og fremgangsmåte for bryting av slike emulsjoner
NO162004B (no)	1989-07-17	Fremgangsmaate til aa demulgere en emulsjon av olje og vann, og kvaternisert polyamidoamin egnet som demulgeringsmiddel.
RU2105788C1 (ru)	1998-02-27	Способ разделения нефтяных эмульсий типа вода-в-нефти
US20040147407A1 (en)	2004-07-29	Polyether polyesters having anionic functionality
US3098827A (en)	1963-07-23	Demulsification of petroleum oil emulsions
NO165639B (no)	1990-12-03	Oksalkylerte polyesteraminer, fremgangsmaate til deres fremstilling, og deres anvendelse.
US2344980A (en)	1944-03-28	Process for breaking petroleum emulsions
NO874722L (no)	1988-05-16	Forgrenede kvaternaere polyoksalkylenblandingspolyestere, fremgangsmaate til deres fremstilling og deres anvendelse.
US2599538A (en)	1952-06-10	Process of demulsifying
US3169118A (en)	1965-02-09	Compositions and processes for breaking petroleum emulsions
US2324491A (en)	1943-07-20	Process for breaking petroleum emulsions
US2713559A (en)	1955-07-19	Process for breaking petroleum emulsions
NO178071B (no)	1995-10-09	Aminfrie forestrede glycidyleter-addisjonsprodukter og anvendelse derav
US2295163A (en)	1942-09-08	Process for breaking petroleum emulsions
US2605233A (en)	1952-07-29	Process for breaking petroleum emulsions
US3061620A (en)	1962-10-30	Polycarboxy acid esters of polyoxyethylated castor oil
US2353700A (en)	1944-07-18	Process for breaking petroleum emulsions
US2353695A (en)	1944-07-18	Process for breaking petroleum emulsions
US3210291A (en)	1965-10-05	Processes for breaking petroleum emulsions with dicarboxy acid esters of sulfated oxyalkylated alkyl phenolformaldehyde resins
US2353699A (en)	1944-07-18	Process for breaking petroleum emulsions
US2324492A (en)	1943-07-20	Process for breaking petroleum emulsions
US2353696A (en)	1944-07-18	Process for breaking petroleum emulsions
US2295164A (en)	1942-09-08	Process for breaking petroleum emulsions