SK159694A3 - Surfactans derived from polyoxyalkylenes and anhydrides of substituted succinic acids and their using - Google Patents

Surfactans derived from polyoxyalkylenes and anhydrides of substituted succinic acids and their using Download PDF

Info

Publication number: SK159694A3
Authority: SK; Slovakia
Prior art keywords: carbon atoms; formula; alkyl group; substituted succinic; value
Prior art date: 1992-06-26

Application number

SK1596-94A

Other languages

English (en)

Slovak (sk)

Inventor

Neil M Carpenter

G Mcgregor

Clive E Wilne

Original Assignee

Ici Plc

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.)

1992-06-26

Filing date

1993-06-25

Publication date

1995-06-07

1993-06-25 Application filed by Ici Plc filed Critical Ici Plc

1995-06-07 Publication of SK159694A3 publication Critical patent/SK159694A3/sk

Links

150000008064 anhydrides Chemical class 0.000 title description 12
235000011044 succinic acid Nutrition 0.000 title description 5
150000003444 succinic acids Chemical class 0.000 title description 3
210000002268 wool Anatomy 0.000 claims abstract description 28
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 23
229920002401 polyacrylamide Polymers 0.000 claims abstract description 7
150000001875 compounds Chemical class 0.000 claims description 60
125000004432 carbon atom Chemical group C* 0.000 claims description 48
125000000217 alkyl group Chemical group 0.000 claims description 44
125000003342 alkenyl group Chemical group 0.000 claims description 25
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 21
239000000203 mixture Substances 0.000 claims description 16
150000001768 cations Chemical class 0.000 claims description 15
238000000034 method Methods 0.000 claims description 11
239000007762 w/o emulsion Substances 0.000 claims description 11
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
150000003443 succinic acid derivatives Chemical class 0.000 claims description 10
239000008346 aqueous phase Substances 0.000 claims description 9
229910052739 hydrogen Inorganic materials 0.000 claims description 9
239000001257 hydrogen Substances 0.000 claims description 8
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 7
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 6
241001494479 Pecora Species 0.000 claims description 6
229910052783 alkali metal Inorganic materials 0.000 claims description 6
-1 alkali metal cation Chemical class 0.000 claims description 6
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
239000011492 sheep wool Substances 0.000 claims description 5
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
229910052799 carbon Inorganic materials 0.000 claims description 3
239000004094 surface-active agent Substances 0.000 abstract description 32
239000000839 emulsion Substances 0.000 abstract description 9
150000002148 esters Chemical class 0.000 abstract description 7
238000009991 scouring Methods 0.000 abstract description 6
150000001408 amides Chemical class 0.000 abstract description 2
RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical class O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 abstract 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 23
238000005406 washing Methods 0.000 description 17
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
239000003795 chemical substances by application Substances 0.000 description 12
239000002904 solvent Substances 0.000 description 11
238000006243 chemical reaction Methods 0.000 description 10
239000003921 oil Substances 0.000 description 10
229920001515 polyalkylene glycol Polymers 0.000 description 10
150000001412 amines Chemical class 0.000 description 8
239000000243 solution Substances 0.000 description 8
239000002253 acid Substances 0.000 description 7
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical group CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
239000000463 material Substances 0.000 description 6
239000012071 phase Substances 0.000 description 6
229920000642 polymer Polymers 0.000 description 6
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
150000005215 alkyl ethers Chemical class 0.000 description 5
239000003599 detergent Substances 0.000 description 5
238000004519 manufacturing process Methods 0.000 description 5
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
239000003054 catalyst Substances 0.000 description 4
239000000835 fiber Substances 0.000 description 4
239000006260 foam Substances 0.000 description 4
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
229920000847 nonoxynol Polymers 0.000 description 4
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 4
229920001983 poloxamer Polymers 0.000 description 4
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
239000000126 substance Substances 0.000 description 4
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 4
238000012360 testing method Methods 0.000 description 4
125000004169 (C1-C6) alkyl group Chemical group 0.000 description 3
YAXXOCZAXKLLCV-UHFFFAOYSA-N 3-dodecyloxolane-2,5-dione Chemical class CCCCCCCCCCCCC1CC(=O)OC1=O YAXXOCZAXKLLCV-UHFFFAOYSA-N 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
239000002202 Polyethylene glycol Substances 0.000 description 3
125000002947 alkylene group Chemical group 0.000 description 3
238000004140 cleaning Methods 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
238000005984 hydrogenation reaction Methods 0.000 description 3
125000001841 imino group Chemical group [H]N=* 0.000 description 3
235000019388 lanolin Nutrition 0.000 description 3
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 3
229920001223 polyethylene glycol Polymers 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
238000000926 separation method Methods 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
150000003505 terpenes Chemical class 0.000 description 3
235000007586 terpenes Nutrition 0.000 description 3
239000001993 wax Substances 0.000 description 3
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
241000004297 Draba Species 0.000 description 2
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
101100420928 Oryza sativa subsp. japonica SE14 gene Proteins 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
230000002378 acidificating effect Effects 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
150000001340 alkali metals Chemical class 0.000 description 2
230000009435 amidation Effects 0.000 description 2
238000007112 amidation reaction Methods 0.000 description 2
125000004429 atom Chemical group 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
229920001400 block copolymer Polymers 0.000 description 2
238000000576 coating method Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
230000032050 esterification Effects 0.000 description 2
238000005886 esterification reaction Methods 0.000 description 2
125000003827 glycol group Chemical group 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
125000004430 oxygen atom Chemical group O* 0.000 description 2
235000011007 phosphoric acid Nutrition 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
238000000746 purification Methods 0.000 description 2
239000000376 reactant Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000001384 succinic acid Substances 0.000 description 2
229940014800 succinic anhydride Drugs 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
238000004566 IR spectroscopy Methods 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 description 1
239000007868 Raney catalyst Substances 0.000 description 1
229910000564 Raney nickel Inorganic materials 0.000 description 1
NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
238000009825 accumulation Methods 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
239000003377 acid catalyst Substances 0.000 description 1
239000013543 active substance Substances 0.000 description 1
230000002411 adverse Effects 0.000 description 1
239000003905 agrochemical Substances 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
150000001346 alkyl aryl ethers Chemical class 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
238000010936 aqueous wash Methods 0.000 description 1
239000002585 base Substances 0.000 description 1
238000006065 biodegradation reaction Methods 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
230000001186 cumulative effect Effects 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
238000007865 diluting Methods 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
238000007720 emulsion polymerization reaction Methods 0.000 description 1
239000003623 enhancer Substances 0.000 description 1
125000004494 ethyl ester group Chemical group 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
238000000605 extraction Methods 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000000446 fuel Substances 0.000 description 1
150000002334 glycols Chemical group 0.000 description 1
239000008233 hard water Substances 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
230000002209 hydrophobic effect Effects 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
238000002372 labelling Methods 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
238000005555 metalworking Methods 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
230000003278 mimic effect Effects 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
230000000269 nucleophilic effect Effects 0.000 description 1
230000009965 odorless effect Effects 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
150000003016 phosphoric acids Chemical class 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000001103 potassium chloride Substances 0.000 description 1
235000011164 potassium chloride Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
229920005604 random copolymer Polymers 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
238000005201 scrubbing Methods 0.000 description 1
238000010008 shearing Methods 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
239000007858 starting material Substances 0.000 description 1
229920006301 statistical copolymer Polymers 0.000 description 1
230000003335 steric effect Effects 0.000 description 1
238000001356 surgical procedure Methods 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
238000010998 test method Methods 0.000 description 1
QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
239000004753 textile Substances 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
239000002699 waste material Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1
235000014101 wine Nutrition 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/22—Amides or hydrazides
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
- 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
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/52—Amides or imides
- C08F20/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
- C08F20/56—Acrylamide; Methacrylamide
- 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
- 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
- C08G65/332—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides, or esters thereof
- 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
- C08G65/333—Polymers modified by chemical after-treatment with organic compounds containing nitrogen
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- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/16—Amines or polyamines
- C—CHEMISTRY; METALLURGY
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- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/34—Higher-molecular-weight carboxylic acid esters
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B11/00—Recovery or refining of other fatty substances, e.g. lanolin or waxes
- 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
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/08—Polycarboxylic acids containing no nitrogen or sulfur
- 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
- C11D1/38—Cationic compounds
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/528—Carboxylic amides (R1-CO-NR2R3), where at least one of the chains R1, R2 or R3 is interrupted by a functional group, e.g. a -NH-, -NR-, -CO-, or -CON- group
- 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
- C11D1/74—Carboxylates or sulfonates esters of polyoxyalkylene glycols
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01C—CHEMICAL OR BIOLOGICAL TREATMENT OF NATURAL FILAMENTARY OR FIBROUS MATERIAL TO OBTAIN FILAMENTS OR FIBRES FOR SPINNING; CARBONISING RAGS TO RECOVER ANIMAL FIBRES
- D01C3/00—Treatment of animal material, e.g. chemical scouring of wool
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L1/00—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods
- D06L1/12—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods using aqueous solvents
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2333/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
- C08J2333/24—Homopolymers or copolymers of amides or imides
- C08J2333/26—Homopolymers or copolymers of acrylamide or methacrylamide

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Materials Engineering (AREA)
Health & Medical Sciences (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
Wood Science & Technology (AREA)
Oil, Petroleum & Natural Gas (AREA)
Textile Engineering (AREA)
Animal Husbandry (AREA)
Molecular Biology (AREA)
Zoology (AREA)
Dispersion Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Detergent Compositions (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Colloid Chemistry (AREA)

SK1596-94A 1992-06-26 1993-06-25 Surfactans derived from polyoxyalkylenes and anhydrides of substituted succinic acids and their using SK159694A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB929213571A GB9213571D0 (en)	1992-06-26	1992-06-26	Surfactants
PCT/GB1993/001335 WO1994000508A1 (en)	1992-06-26	1993-06-25	Surfactants derived from polyoxyalkylenes and substituted succinic anhydrides

Publications (1)

Publication Number	Publication Date
SK159694A3 true SK159694A3 (en)	1995-06-07

Family

ID=10717766

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK1596-94A SK159694A3 (en)	1992-06-26	1993-06-25	Surfactans derived from polyoxyalkylenes and anhydrides of substituted succinic acids and their using

Country Status (15)

Country	Link
EP (1)	EP0647248A1 (ja)
JP (1)	JPH07508546A (ja)
KR (1)	KR950702215A (ja)
AU (1)	AU679918B2 (ja)
CA (1)	CA2139003A1 (ja)
CZ (1)	CZ328094A3 (ja)
FI (1)	FI946075A0 (ja)
GB (2)	GB9213571D0 (ja)
HU (1)	HUT68780A (ja)
NZ (1)	NZ253297A (ja)
RU (1)	RU2118641C1 (ja)
SK (1)	SK159694A3 (ja)
TW (1)	TW256854B (ja)
WO (1)	WO1994000508A1 (ja)
ZA (1)	ZA934479B (ja)

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US6780209B1 (en)	2000-01-24	2004-08-24	The Lubrizol Corporation	Partially dehydrated reaction product process for making same, and emulsion containing same
FR2811564B1 (fr)	2000-07-13	2002-12-27	Oreal	Nanoemulsion contenant des polymeres non ioniques, et ses utilisations notamment dans les domaines cosmetique, dermatologique, pharmaceutique et/ou ophtalmologique
GB0101771D0 (en)	2001-01-24	2001-03-07	Ici Plc	Anionic surfactants
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CN102257111B (zh)	2008-12-25	2014-06-11	陶氏环球技术有限责任公司	具有宽pH稳定性的表面活性剂组合物
FR2954107B1 (fr)	2009-12-23	2012-04-20	Oreal	Composition cosmetique sous forme de nanoemulsion contenant un alcane lineaire volatil
CN103189409B (zh) *	2010-09-01	2015-11-25	巴斯夫欧洲公司	用于增溶微溶性活性成分的两亲物
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US10028895B2 (en)	2013-05-17	2018-07-24	L'oreal	Emulsion stabilization via silicilic acid complexation
US9452406B2 (en)	2013-05-17	2016-09-27	L'oreal	Bubble encapsulation via silicilic acid complexation
US9433578B2 (en)	2013-05-17	2016-09-06	L'oreal	Stable bubbles via particle absorption by electrostatic interaction
US20160192642A1 (en)	2013-08-14	2016-07-07	Croda, Inc.	Spray drift reduction
RU2631235C2 (ru)	2013-08-14	2017-09-20	Крода, Инк.	Комбинация вспомогательных веществ
ES2875061T3 (es)	2013-10-18	2021-11-08	Croda Inc	Adyuvantes de ésteres de sorbato alcoxilados
GB201403599D0 (en)	2014-02-28	2014-04-16	Croda Int Plc	Micronutrient compositions
EP3075436B1 (en) *	2015-04-02	2018-08-01	Afton Chemical Limited	Diesel exhaust fluid solutions and methods of using the same
DE102015015911A1 (de)	2015-12-09	2017-06-14	Nanopartica Gmbh	Hocheffizientes Nanotransportsystem durch kovalent gebundene Alkenylbernsteinsäureanhydrid-Derivate an dendritischen Polymeren
GB201609160D0 (en)	2016-05-25	2016-07-06	Croda Europ Ltd	Polymeric coating compositions
CN109310080A (zh)	2016-07-01	2019-02-05	禾大公司	喷雾漂移减少
JP6841610B2 (ja) *	2016-07-15	2021-03-10	松本油脂製薬株式会社	洗浄剤組成物及び洗浄方法
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1992
- 1992-06-26 GB GB929213571A patent/GB9213571D0/en active Pending
1993
- 1993-06-22 ZA ZA934479A patent/ZA934479B/xx unknown
- 1993-06-24 GB GB939313096A patent/GB9313096D0/en active Pending
- 1993-06-25 AU AU43505/93A patent/AU679918B2/en not_active Ceased
- 1993-06-25 HU HU9403701A patent/HUT68780A/hu unknown
- 1993-06-25 JP JP6502165A patent/JPH07508546A/ja active Pending
- 1993-06-25 RU RU94046395A patent/RU2118641C1/ru active
- 1993-06-25 SK SK1596-94A patent/SK159694A3/sk unknown
- 1993-06-25 CA CA002139003A patent/CA2139003A1/en not_active Abandoned
- 1993-06-25 KR KR1019940704735A patent/KR950702215A/ko not_active IP Right Cessation
- 1993-06-25 EP EP93913432A patent/EP0647248A1/en not_active Withdrawn
- 1993-06-25 NZ NZ253297A patent/NZ253297A/en unknown
- 1993-06-25 WO PCT/GB1993/001335 patent/WO1994000508A1/en not_active Application Discontinuation
- 1993-06-25 CZ CZ943280A patent/CZ328094A3/cs unknown
- 1993-06-26 TW TW082105101A patent/TW256854B/zh active
1994
- 1994-12-23 FI FI946075A patent/FI946075A0/fi unknown

Also Published As

Publication number	Publication date
CA2139003A1 (en)	1994-01-06
AU4350593A (en)	1994-01-24
CZ328094A3 (en)	1995-06-14
FI946075A (fi)	1994-12-23
HUT68780A (en)	1995-07-28
RU94046395A (ru)	1996-11-20
GB9213571D0 (en)	1992-08-12
GB9313096D0 (en)	1993-08-11
WO1994000508A1 (en)	1994-01-06
JPH07508546A (ja)	1995-09-21
AU679918B2 (en)	1997-07-17
KR950702215A (ko)	1995-06-19
NZ253297A (en)	1997-02-24
TW256854B (ja)	1995-09-11
EP0647248A1 (en)	1995-04-12
RU2118641C1 (ru)	1998-09-10
ZA934479B (en)	1995-03-22
FI946075A0 (fi)	1994-12-23

Publication	Publication Date	Title
SK159694A3 (en)	1995-06-07	Surfactans derived from polyoxyalkylenes and anhydrides of substituted succinic acids and their using
FI110775B (fi)	2003-03-31	2-propyyliheptanolin alkoksylaatin käyttö
US6204297B1 (en)	2001-03-20	Nonionic gemini surfactants
US5914310A (en)	1999-06-22	Amphoteric surfactants having multiple hydrophobic and hydrophilic groups
US5750492A (en)	1998-05-12	Surfactants based on quaternary ammonium compounds preparation processes softening bases and compositions derived
EP0199131A2 (en)	1986-10-29	Surfactants derived from citric acid
JPH08103646A (ja)	1996-04-23	アニオン界面活性剤およびそれを含む洗浄剤組成物
CN103476913A (zh)	2013-12-25	可稀释的清洁组合物和使用方法
SK285356B6 (sk)	2006-11-03	Palivové kompozície obsahujúce propoxylát, palivové aditívne zmesi a ich použitie
DE112006003163T5 (de)	2009-01-29	Grenzflächenaktives Polymer und seine Verwendung in einer Wasser-in-Öl-Emulsion
EP0038862B1 (en)	1984-02-01	Compositions containing amido amine salts, and their use as fabric softeners
EP1042266B1 (en)	2002-09-04	An ortho ester-based surfactant, its preparation and use
JPH06507164A (ja)	1994-08-11	アミド製品混合物の製造方法、アミド製品混合物およびその使用
US4353834A (en)	1982-10-12	Carbonate and carboxylic acid ester group-containing non-ionic surface-active agents
AU2002324404B2 (en)	2007-12-06	A nitrogen-containing ortho ester-based surfactant, its preparation and use
US2491478A (en)	1949-12-20	Polyalcohol-fatty acid-aliphatic amine combinations useful as textile assistants andprocess of producing the same
GB1592203A (en)	1981-07-01	Non-ionic surfactants
JPH07502269A (ja)	1995-03-09	親水性化トリグリセリドの製法
JPH09506384A (ja)	1997-06-24	非イオン性洗剤混合物
CN101711275A (zh)	2010-05-19	可生物降解的清洁组合物
JP3256747B2 (ja)	2002-02-12	液体柔軟剤組成物
JPH07505181A (ja)	1995-06-08	液体洗剤
JPH027694B2 (ja)	1990-02-20
JPS608279B2 (ja)	1985-03-01	液体洗浄剤組成物
JP4889895B2 (ja)	2012-03-07	界面活性剤