SE513181C2 - En ortoesterbaserad tensid, dess tillverkning och användning - Google Patents

En ortoesterbaserad tensid, dess tillverkning och användning

Info

Publication number: SE513181C2
Authority: SE; Sweden
Prior art keywords: orthoester; carbon atoms; surfactant; group; emulsion
Prior art date: 1997-12-19

Application number

SE9704755A

Other languages

English (en)

Swedish (sv)

Other versions

SE9704755L (sv

SE9704755D0 (sv

Inventor

Karin Bergstroem

Per-Erik Hellberg

Original Assignee

Akzo Nobel Nv

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.)

1997-12-19

Filing date

1997-12-19

Publication date

2000-07-24

1997-12-19 Application filed by Akzo Nobel Nv filed Critical Akzo Nobel Nv

1997-12-19 Priority to SE9704755A priority Critical patent/SE513181C2/sv

1997-12-19 Publication of SE9704755D0 publication Critical patent/SE9704755D0/xx

1998-12-08 Priority to AU19879/99A priority patent/AU739404B2/en

1998-12-08 Priority to CNB988124300A priority patent/CN1140491C/zh

1998-12-08 Priority to KR1020007006574A priority patent/KR20010033190A/ko

1998-12-08 Priority to BRPI9813810-3A priority patent/BR9813810B1/pt

1998-12-08 Priority to EP98964585A priority patent/EP1042266B1/de

1998-12-08 Priority to AT98964585T priority patent/ATE223367T1/de

1998-12-08 Priority to JP2000525362A priority patent/JP4386576B2/ja

1998-12-08 Priority to DE69807749T priority patent/DE69807749T2/de

1998-12-08 Priority to PCT/SE1998/002239 priority patent/WO1999032424A1/en

1998-12-08 Priority to CA002310646A priority patent/CA2310646A1/en

1999-06-20 Publication of SE9704755L publication Critical patent/SE9704755L/

2000-07-24 Publication of SE513181C2 publication Critical patent/SE513181C2/sv

2003-08-18 Priority to US10/642,882 priority patent/US7002045B2/en

Links

150000002905 orthoesters Chemical class 0.000 title claims abstract description 57
239000004094 surface-active agent Substances 0.000 title abstract description 61
238000004519 manufacturing process Methods 0.000 title description 3
230000002209 hydrophobic effect Effects 0.000 claims abstract description 19
238000000034 method Methods 0.000 claims description 29
239000000839 emulsion Substances 0.000 claims description 27
125000004432 carbon atom Chemical group C* 0.000 claims description 19
125000000217 alkyl group Chemical group 0.000 claims description 13
238000004140 cleaning Methods 0.000 claims description 9
150000001298 alcohols Chemical class 0.000 claims description 8
125000001931 aliphatic group Chemical group 0.000 claims description 7
125000005529 alkyleneoxy group Chemical group 0.000 claims description 6
239000006185 dispersion Substances 0.000 claims description 6
230000001804 emulsifying effect Effects 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
-1 ethyleneoxy groups Chemical group 0.000 claims description 5
239000002270 dispersing agent Substances 0.000 claims description 4
239000003995 emulsifying agent Substances 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
239000002761 deinking Substances 0.000 claims description 3
238000004043 dyeing Methods 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
239000000376 reactant Substances 0.000 claims description 3
239000003090 pesticide formulation Substances 0.000 claims description 2
102200014657 rs121434437 Human genes 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
230000008020 evaporation Effects 0.000 claims 1
238000001704 evaporation Methods 0.000 claims 1
125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
239000000203 mixture Substances 0.000 description 28
238000009472 formulation Methods 0.000 description 21
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 20
238000000926 separation method Methods 0.000 description 14
GKASDNZWUGIAMG-UHFFFAOYSA-N triethyl orthoformate Chemical compound CCOC(OCC)OCC GKASDNZWUGIAMG-UHFFFAOYSA-N 0.000 description 14
239000003921 oil Substances 0.000 description 11
235000019198 oils Nutrition 0.000 description 11
YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 10
239000002736 nonionic surfactant Substances 0.000 description 10
238000006243 chemical reaction Methods 0.000 description 8
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
229920001223 polyethylene glycol Polymers 0.000 description 7
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 6
239000002202 Polyethylene glycol Substances 0.000 description 6
DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 6
239000012071 phase Substances 0.000 description 6
239000008346 aqueous phase Substances 0.000 description 5
239000007853 buffer solution Substances 0.000 description 5
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 5
238000005259 measurement Methods 0.000 description 5
239000000047 product Substances 0.000 description 5
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 4
125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 4
238000003776 cleavage reaction Methods 0.000 description 4
230000000694 effects Effects 0.000 description 4
238000002474 experimental method Methods 0.000 description 4
230000007062 hydrolysis Effects 0.000 description 4
238000006460 hydrolysis reaction Methods 0.000 description 4
230000007017 scission Effects 0.000 description 4
239000004753 textile Substances 0.000 description 4
239000002351 wastewater Substances 0.000 description 4
238000005160 1H NMR spectroscopy Methods 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
235000010469 Glycine max Nutrition 0.000 description 3
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 3
239000007788 liquid Substances 0.000 description 3
229940098779 methanesulfonic acid Drugs 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
238000005406 washing Methods 0.000 description 3
SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 2
BAECOWNUKCLBPZ-HIUWNOOHSA-N Triolein Natural products O([C@H](OCC(=O)CCCCCCC/C=C\CCCCCCCC)COC(=O)CCCCCCC/C=C\CCCCCCCC)C(=O)CCCCCCC/C=C\CCCCCCCC BAECOWNUKCLBPZ-HIUWNOOHSA-N 0.000 description 2
PHYFQTYBJUILEZ-UHFFFAOYSA-N Trioleoylglycerol Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCCCCCCCC)COC(=O)CCCCCCCC=CCCCCCCCC PHYFQTYBJUILEZ-UHFFFAOYSA-N 0.000 description 2
230000002378 acidificating effect Effects 0.000 description 2
JBTHDAVBDKKSRW-UHFFFAOYSA-N chembl1552233 Chemical compound CC1=CC(C)=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 JBTHDAVBDKKSRW-UHFFFAOYSA-N 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 description 2
239000007857 degradation product Substances 0.000 description 2
XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 2
229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 2
238000004945 emulsification Methods 0.000 description 2
238000005187 foaming Methods 0.000 description 2
239000004519 grease Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
239000010893 paper waste Substances 0.000 description 2
150000003138 primary alcohols Chemical class 0.000 description 2
229940073450 sudan red Drugs 0.000 description 2
239000008399 tap water Substances 0.000 description 2
235000020679 tap water Nutrition 0.000 description 2
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 2
NDQXKKFRNOPRDW-UHFFFAOYSA-N 1,1,1-triethoxyethane Chemical compound CCOC(C)(OCC)OCC NDQXKKFRNOPRDW-UHFFFAOYSA-N 0.000 description 1
238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 1
240000002791 Brassica napus Species 0.000 description 1
235000004977 Brassica sinapistrum Nutrition 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000004435 Oxo alcohol Substances 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
229920000297 Rayon Polymers 0.000 description 1
239000002253 acid Substances 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
229960004543 anhydrous citric acid Drugs 0.000 description 1
TZIHFWKZFHZASV-UHFFFAOYSA-N anhydrous methyl formate Natural products COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 1
238000006065 biodegradation reaction Methods 0.000 description 1
229960004106 citric acid Drugs 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000002283 diesel fuel Substances 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000000835 fiber Substances 0.000 description 1
230000004992 fission Effects 0.000 description 1
239000012530 fluid Substances 0.000 description 1
WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
239000010931 gold Substances 0.000 description 1
229910052737 gold Inorganic materials 0.000 description 1
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
150000004677 hydrates Chemical class 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
239000012875 nonionic emulsifier Substances 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002092 orthoester group Chemical group 0.000 description 1
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000013558 reference substance Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000003760 tallow Substances 0.000 description 1
239000012085 test solution Substances 0.000 description 1
RYCLIXPGLDDLTM-UHFFFAOYSA-J tetrapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O RYCLIXPGLDDLTM-UHFFFAOYSA-J 0.000 description 1
239000003440 toxic substance Substances 0.000 description 1
229940117972 triolein Drugs 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000003981 vehicle Substances 0.000 description 1
239000008096 xylene 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/331—Polymers modified by chemical after-treatment with organic compounds containing oxygen
- C08G65/3311—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing a hydroxy group
- C08G65/3312—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing a hydroxy group acyclic
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/32—Compounds having groups or groups
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/331—Polymers modified by chemical after-treatment with organic compounds containing oxygen
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/667—Neutral esters, e.g. sorbitan esters

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Engineering & Computer Science (AREA)
Life Sciences & Earth Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Detergent Compositions (AREA)
Polyethers (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

SE9704755A 1997-12-19 1997-12-19 En ortoesterbaserad tensid, dess tillverkning och användning SE513181C2 (sv)

Priority Applications (12)

Application Number	Priority Date	Filing Date	Title
SE9704755A SE513181C2 (sv)	1997-12-19	1997-12-19	En ortoesterbaserad tensid, dess tillverkning och användning
CA002310646A CA2310646A1 (en)	1997-12-19	1998-12-08	An ortho ester-based surfactant, its preparation and use
AT98964585T ATE223367T1 (de)	1997-12-19	1998-12-08	Ein auf ortho-ester-struktur basierendes oberflächenaktives mittel, seine herstellung und verwendung
CNB988124300A CN1140491C (zh)	1997-12-19	1998-12-08	基于原酸酯的表面活性剂及其制备和应用
KR1020007006574A KR20010033190A (ko)	1997-12-19	1998-12-08	오르토 에스테르계 계면활성제, 이의 제법 및 용도
BRPI9813810-3A BR9813810B1 (pt)	1997-12-19	1998-12-08	surfactante baseado em um orto éster, a sua preparação e o seu uso.
EP98964585A EP1042266B1 (de)	1997-12-19	1998-12-08	Ein auf ortho-ester-struktur basierendes oberflächenaktives mittel, seine herstellung und verwendung
AU19879/99A AU739404B2 (en)	1997-12-19	1998-12-08	An ortho ester-based surfactant, its preparation and use
JP2000525362A JP4386576B2 (ja)	1997-12-19	1998-12-08	オルトエステルを主成分とする界面活性剤、その調製および使用
DE69807749T DE69807749T2 (de)	1997-12-19	1998-12-08	Ein auf ortho-ester-struktur basierendes oberflächenaktives mittel, seine herstellung und verwendung
PCT/SE1998/002239 WO1999032424A1 (en)	1997-12-19	1998-12-08	An ortho ester-based surfactant, its preparation and use
US10/642,882 US7002045B2 (en)	1997-12-19	2003-08-18	Ortho ester-based surfactant, its preparation and use

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
SE9704755A SE513181C2 (sv)	1997-12-19	1997-12-19	En ortoesterbaserad tensid, dess tillverkning och användning

Publications (3)

Publication Number	Publication Date
SE9704755D0 SE9704755D0 (sv)	1997-12-19
SE9704755L SE9704755L (sv)	1999-06-20
SE513181C2 true SE513181C2 (sv)	2000-07-24

Family

ID=20409462

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE9704755A SE513181C2 (sv)	1997-12-19	1997-12-19	En ortoesterbaserad tensid, dess tillverkning och användning

Country Status (12)

Country	Link
US (1)	US7002045B2 (de)
EP (1)	EP1042266B1 (de)
JP (1)	JP4386576B2 (de)
KR (1)	KR20010033190A (de)
CN (1)	CN1140491C (de)
AT (1)	ATE223367T1 (de)
AU (1)	AU739404B2 (de)
BR (1)	BR9813810B1 (de)
CA (1)	CA2310646A1 (de)
DE (1)	DE69807749T2 (de)
SE (1)	SE513181C2 (de)
WO (1)	WO1999032424A1 (de)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
SE523426C2 (sv) *	2001-08-23	2004-04-20	Akzo Nobel Nv	En kväveinnehållande ortoesterbaserad tensid, dess tillverkning och användning
ATE412684T1 (de)	2002-09-09	2008-11-15	Nektar Therapeutics Al Corp	Verfahren zur herstellung von wasserlöslichen polymerderivaten mit terminalen carboxylgruppen
DE10350105A1 (de) *	2003-10-27	2005-05-25	Basf Ag	Verfahren zur Herstellung von Orthoestern
US20070066493A1 (en) *	2005-09-22	2007-03-22	Halliburton Energy Services, Inc.	Orthoester-based surfactants and associated methods
CA2559675C (en) *	2005-09-22	2009-10-27	Halliburton Energy Services, Inc.	Orthoester-based surfactants and associated methods
US7713916B2 (en) *	2005-09-22	2010-05-11	Halliburton Energy Services, Inc.	Orthoester-based surfactants and associated methods
DE112007000772T5 (de)	2006-04-07	2009-02-05	Akzo Nobel N.V.	Umweltfreundliche Öl/Wasser-Demulgatoren
CN101421376B (zh) *	2006-04-07	2013-09-18	阿克佐诺贝尔股份有限公司	环境友好的油/水破乳剂
JP5172541B2 (ja) *	2008-08-28	2013-03-27	富士フイルム株式会社	粉末用表面改質剤ならびにそれを含む磁性塗料および非磁性塗料、磁気記録媒体およびその製造方法
US8853299B2 (en) *	2009-10-06	2014-10-07	Amcol International Corp.	Lignite-based urethane resins with enhanced suspension properties and foundry sand binder performance
US8426494B2 (en) *	2009-10-06	2013-04-23	Amcol International Corp.	Lignite urethane based resins for enhanced foundry sand performance
US8436073B2 (en)	2009-10-06	2013-05-07	Amcol International	Lignite-based foundry resins
US8309620B2 (en) *	2009-10-06	2012-11-13	Amcol International Corp.	Lignite-based urethane resins with enhanced suspension properties and foundry sand binder performance
US8623959B2 (en) *	2009-10-06	2014-01-07	Joseph M. Fuqua	Non-veining urethane resins for foundry sand casting
US8317973B2 (en)	2009-11-11	2012-11-27	Kemira Chemical, Inc.	Polyester surfactants for deinking
EP4056550A1 (de) *	2021-03-12	2022-09-14	Clariant International Ltd	Verfahren zur herstellung von orthoestern

Family Cites Families (6)

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Publication number	Priority date	Publication date	Assignee	Title
US2867667A (en) *	1958-05-29	1959-01-06	Cities Service Res & Dev Co	Olefin oxide ortho ester condensation products
US3903006A (en) *	1969-12-16	1975-09-02	Castrol Ltd	Synthetic esters
GB1513881A (en) *	1974-07-12	1978-06-14	Castrol Ltd	Hydraulic fluids
EP0054366A3 (de) *	1980-12-15	1982-08-11	Imperial Chemical Industries Plc	Tensio-aktive Substanzen und die sie enthaltenden Zusammensetzungen
CH684933A5 (de) *	1992-04-01	1995-02-15	Ciba Geigy Ag	Schaumarme oberflächenaktive Verbindungen.
SE506983C2 (sv) *	1996-07-02	1998-03-09	Akzo Nobel Nv	Ortoesterbaserad polymer, förfarande för dess framställning och användning därav

1997
- 1997-12-19 SE SE9704755A patent/SE513181C2/sv not_active IP Right Cessation
1998
- 1998-12-08 DE DE69807749T patent/DE69807749T2/de not_active Expired - Lifetime
- 1998-12-08 AU AU19879/99A patent/AU739404B2/en not_active Ceased
- 1998-12-08 JP JP2000525362A patent/JP4386576B2/ja not_active Expired - Fee Related
- 1998-12-08 BR BRPI9813810-3A patent/BR9813810B1/pt not_active IP Right Cessation
- 1998-12-08 WO PCT/SE1998/002239 patent/WO1999032424A1/en not_active Ceased
- 1998-12-08 AT AT98964585T patent/ATE223367T1/de not_active IP Right Cessation
- 1998-12-08 KR KR1020007006574A patent/KR20010033190A/ko not_active Withdrawn
- 1998-12-08 CA CA002310646A patent/CA2310646A1/en not_active Abandoned
- 1998-12-08 CN CNB988124300A patent/CN1140491C/zh not_active Expired - Fee Related
- 1998-12-08 EP EP98964585A patent/EP1042266B1/de not_active Expired - Lifetime
2003
- 2003-08-18 US US10/642,882 patent/US7002045B2/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
CN1282313A (zh)	2001-01-31
US7002045B2 (en)	2006-02-21
EP1042266B1 (de)	2002-09-04
EP1042266A1 (de)	2000-10-11
CN1140491C (zh)	2004-03-03
JP4386576B2 (ja)	2009-12-16
SE9704755L (sv)	1999-06-20
DE69807749T2 (de)	2003-05-08
KR20010033190A (ko)	2001-04-25
DE69807749D1 (de)	2002-10-10
AU739404B2 (en)	2001-10-11
AU1987999A (en)	1999-07-12
JP2001526250A (ja)	2001-12-18
ATE223367T1 (de)	2002-09-15
WO1999032424A1 (en)	1999-07-01
BR9813810A (pt)	2000-10-03
BR9813810B1 (pt)	2009-12-01
CA2310646A1 (en)	1999-07-01
SE9704755D0 (sv)	1997-12-19
US20040039235A1 (en)	2004-02-26

Legal Events

Date	Code	Title	Description
2007-08-21	NUG	Patent has lapsed

Publication	Publication Date	Title
SE513181C2 (sv)	2000-07-24	En ortoesterbaserad tensid, dess tillverkning och användning
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WO1992021743A1 (en)	1992-12-10	Rinsing composition
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