BE898441A - Emulsionnant non ionique et compositions d'un anhydride succinique substitué avec cet émulsionnant. - Google Patents

Emulsionnant non ionique et compositions d'un anhydride succinique substitué avec cet émulsionnant. Download PDF

Info

Publication number: BE898441A
Authority: BE; Belgium
Prior art keywords: sep; emulsifier; water; succinic anhydride; radicals
Prior art date: 1982-12-13

Application number

BE0/212035A

Other languages

English (en)

French (fr)

Inventor

W A Sweeney

Original Assignee

Chevron Res

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.)

1982-12-13

Filing date

1983-12-13

Publication date

1984-03-30

1983-12-13 Application filed by Chevron Res filed Critical Chevron Res

1984-03-30 Publication of BE898441A publication Critical patent/BE898441A/fr

Links

239000003995 emulsifying agent Substances 0.000 title claims abstract description 81
239000000203 mixture Substances 0.000 title claims abstract description 69
229940014800 succinic anhydride Drugs 0.000 title claims abstract description 28
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical group ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 title claims abstract description 22
239000012875 nonionic emulsifier Substances 0.000 title claims abstract description 7
239000000839 emulsion Substances 0.000 claims abstract description 40
238000004513 sizing Methods 0.000 claims abstract description 37
150000001875 compounds Chemical class 0.000 claims abstract description 21
230000002209 hydrophobic effect Effects 0.000 claims abstract description 18
238000000034 method Methods 0.000 claims abstract description 18
150000008064 anhydrides Chemical class 0.000 claims abstract description 14
230000008569 process Effects 0.000 claims abstract description 9
239000007795 chemical reaction product Substances 0.000 claims abstract description 5
-1 amino, amine oxide Chemical compound 0.000 claims description 34
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 32
229920001223 polyethylene glycol Polymers 0.000 claims description 28
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 27
125000004432 carbon atom Chemical group C* 0.000 claims description 16
238000006243 chemical reaction Methods 0.000 claims description 13
239000000463 material Substances 0.000 claims description 13
125000001424 substituent group Chemical group 0.000 claims description 13
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 12
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 10
ORTFAQDWJHRMNX-UHFFFAOYSA-M oxidooxomethyl Chemical compound [O-][C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-M 0.000 claims description 10
239000002202 Polyethylene glycol Substances 0.000 claims description 9
150000001336 alkenes Chemical class 0.000 claims description 8
239000000470 constituent Substances 0.000 claims description 8
125000000217 alkyl group Chemical group 0.000 claims description 7
125000003342 alkenyl group Chemical group 0.000 claims description 6
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 6
239000007788 liquid Substances 0.000 claims description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
150000003462 sulfoxides Chemical class 0.000 claims description 3
125000003396 thiol group Chemical group [H]S* 0.000 claims 1
239000003795 chemical substances by application Substances 0.000 description 35
239000000123 paper Substances 0.000 description 23
150000003254 radicals Chemical class 0.000 description 18
239000000047 product Substances 0.000 description 13
125000002091 cationic group Chemical group 0.000 description 10
239000003153 chemical reaction reagent Substances 0.000 description 9
239000000835 fiber Substances 0.000 description 8
238000010438 heat treatment Methods 0.000 description 8
150000002433 hydrophilic molecules Chemical class 0.000 description 8
238000010411 cooking Methods 0.000 description 7
229920001131 Pulp (paper) Polymers 0.000 description 6
229940113116 polyethylene glycol 1000 Drugs 0.000 description 6
238000012360 testing method Methods 0.000 description 6
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
238000003756 stirring Methods 0.000 description 4
229920000881 Modified starch Polymers 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
101100068077 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GCN2 gene Proteins 0.000 description 3
229920002472 Starch Polymers 0.000 description 3
229920002877 acrylic styrene acrylonitrile Polymers 0.000 description 3
239000000654 additive Substances 0.000 description 3
229940037003 alum Drugs 0.000 description 3
230000008901 benefit Effects 0.000 description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
239000003054 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
239000003599 detergent Substances 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
230000001804 emulsifying effect Effects 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
239000004744 fabric Substances 0.000 description 3
239000006260 foam Substances 0.000 description 3
238000005187 foaming Methods 0.000 description 3
235000019426 modified starch Nutrition 0.000 description 3
229920002523 polyethylene Glycol 1000 Polymers 0.000 description 3
238000000926 separation method Methods 0.000 description 3
235000019698 starch Nutrition 0.000 description 3
239000000126 substance Substances 0.000 description 3
SXYRTDICSOVQNZ-UHFFFAOYSA-N 1-(2-methoxyethoxy)ethanol Chemical compound COCCOC(C)O SXYRTDICSOVQNZ-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
229920003043 Cellulose fiber Polymers 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
239000012736 aqueous medium Substances 0.000 description 2
239000007853 buffer solution Substances 0.000 description 2
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000004945 emulsification Methods 0.000 description 2
239000000945 filler Substances 0.000 description 2
239000012467 final product Substances 0.000 description 2
239000008233 hard water Substances 0.000 description 2
DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
230000007062 hydrolysis Effects 0.000 description 2
238000006460 hydrolysis reaction Methods 0.000 description 2
238000002329 infrared spectrum Methods 0.000 description 2
239000000976 ink Substances 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
239000002736 nonionic surfactant Substances 0.000 description 2
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 2
239000000049 pigment Substances 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
239000008107 starch Substances 0.000 description 2
RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical class O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
239000008399 tap water Substances 0.000 description 2
235000020679 tap water Nutrition 0.000 description 2
239000004711 α-olefin Substances 0.000 description 2
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
BZJTUOGZUKFLQT-UHFFFAOYSA-N 1,3,5,7-tetramethylcyclooctane Chemical group CC1CC(C)CC(C)CC(C)C1 BZJTUOGZUKFLQT-UHFFFAOYSA-N 0.000 description 1
CDBMNYGKGNXEIG-UHFFFAOYSA-N 1,3-bis(diethylamino)propan-2-ol Chemical compound CCN(CC)CC(O)CN(CC)CC CDBMNYGKGNXEIG-UHFFFAOYSA-N 0.000 description 1
NCXUNZWLEYGQAH-UHFFFAOYSA-N 1-(dimethylamino)propan-2-ol Chemical compound CC(O)CN(C)C NCXUNZWLEYGQAH-UHFFFAOYSA-N 0.000 description 1
XSXWOBXNYNULJG-UHFFFAOYSA-N 2-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound CC(C)(C)CC(C)(C)C1=CC=CC=C1O XSXWOBXNYNULJG-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
229920002261 Corn starch Polymers 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
239000004831 Hot glue Substances 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
240000003183 Manihot esculenta Species 0.000 description 1
235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
229920000297 Rayon Polymers 0.000 description 1
241001138418 Sequoia sempervirens Species 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
230000009102 absorption Effects 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
230000032683 aging Effects 0.000 description 1
238000007605 air drying Methods 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
230000004075 alteration Effects 0.000 description 1
ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
239000002585 base Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
230000000903 blocking effect Effects 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
229910001424 calcium ion Inorganic materials 0.000 description 1
239000001175 calcium sulphate Substances 0.000 description 1
235000011132 calcium sulphate Nutrition 0.000 description 1
235000014633 carbohydrates Nutrition 0.000 description 1
150000001720 carbohydrates Chemical class 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
230000008859 change Effects 0.000 description 1
229940055042 chromic sulfate Drugs 0.000 description 1
GRWVQDDAKZFPFI-UHFFFAOYSA-H chromium(III) sulfate Chemical compound [Cr+3].[Cr+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRWVQDDAKZFPFI-UHFFFAOYSA-H 0.000 description 1
229910000356 chromium(III) sulfate Inorganic materials 0.000 description 1
239000011696 chromium(III) sulphate Substances 0.000 description 1
235000015217 chromium(III) sulphate Nutrition 0.000 description 1
239000004927 clay Substances 0.000 description 1
229910052570 clay Inorganic materials 0.000 description 1
238000004737 colorimetric analysis Methods 0.000 description 1
239000013065 commercial product Substances 0.000 description 1
239000008120 corn starch Substances 0.000 description 1
230000001186 cumulative effect Effects 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
239000000539 dimer Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
238000009826 distribution Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 description 1
239000003292 glue Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
239000012535 impurity Substances 0.000 description 1
239000002655 kraft paper Substances 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
229910001425 magnesium ion Inorganic materials 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
235000009973 maize Nutrition 0.000 description 1
238000005259 measurement Methods 0.000 description 1
239000002609 medium Substances 0.000 description 1
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
235000013919 monopotassium glutamate Nutrition 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
125000006353 oxyethylene group Chemical group 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
238000012797 qualification Methods 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000004627 regenerated cellulose Substances 0.000 description 1
238000011160 research Methods 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000013535 sea water Substances 0.000 description 1
238000010008 shearing Methods 0.000 description 1
229910001388 sodium aluminate Inorganic materials 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
235000000346 sugar Nutrition 0.000 description 1
150000008163 sugars Chemical class 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
229910021653 sulphate ion Inorganic materials 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
239000012209 synthetic fiber Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
229920001187 thermosetting polymer Polymers 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
238000012549 training Methods 0.000 description 1
230000000007 visual effect Effects 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000002023 wood Substances 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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/02—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
- C07C57/13—Dicarboxylic acids
- 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
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/03—Non-macromolecular organic compounds
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/03—Non-macromolecular organic compounds
- D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
- D21H17/14—Carboxylic acids; Derivatives thereof
- D21H17/15—Polycarboxylic acids, e.g. maleic acid

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
General Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Paper (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

BE0/212035A 1982-12-13 1983-12-13 Emulsionnant non ionique et compositions d'un anhydride succinique substitué avec cet émulsionnant. BE898441A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US44932482A	1982-12-13	1982-12-13

Publications (1)

Publication Number	Publication Date
BE898441A true BE898441A (fr)	1984-03-30

Family

ID=23783737

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BE0/212035A BE898441A (fr)	1982-12-13	1983-12-13	Emulsionnant non ionique et compositions d'un anhydride succinique substitué avec cet émulsionnant.

Country Status (8)

Country	Link
JP (1)	JPS59115733A (de)
BE (1)	BE898441A (de)
DE (1)	DE3345058A1 (de)
FR (1)	FR2537454B1 (de)
GB (1)	GB2131820B (de)
IL (1)	IL70368A (de)
NL (1)	NL8304253A (de)
SE (1)	SE459789B (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5872149A (en) *	1995-02-15	1999-02-16	Basf Aktiengesellschaft	Alk(en)yldicarboxylic acid bisesters, their use, and processes for their preparation

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ZA852200B (en) *	1984-04-09	1986-11-26	Colgate Palmolive Co	Liquid laundry detergent composition
JPS626995A (ja) *	1985-06-28	1987-01-13	ハリマ化成株式会社	製紙用サイズ剤
GB8522844D0 (en) *	1985-09-16	1985-10-23	Albright & Wilson	Dispersible active sizing compositions
GB9213571D0 (en) *	1992-06-26	1992-08-12	Ici Plc	Surfactants
FR2694213B1 (fr) *	1992-08-03	1994-10-14	Inst Francais Du Petrole	Méthode pour réduire la tendance à l'agglomération des hydrates dans des effluents de production.
GB9317476D0 (en) *	1993-08-23	1993-10-06	Ici Plc	Surfactants
AU1713495A (en) *	1994-02-24	1995-09-11	Imperial Chemical Industries Plc	Adjuvant compositions
FR2750044A1 (fr) *	1996-06-21	1997-12-26	Oreal	Utilisation de derives de l'anhydride succinique dans des compositions de nettoyage de la peau
GB9905055D0 (en) *	1999-03-05	1999-04-28	Castrol Ltd	A waste-treatable lubricant
FR2804015B1 (fr)	2000-01-21	2005-12-23	Oreal	Nanoemulsion contenant des lipides amphiphiles et un polymere non ionique et utilisations
DE10147650A1 (de) *	2001-09-27	2003-04-10	Basf Ag	Hydrophile Emulgatoren auf Basis von Polyisobutylen
WO2007131860A1 (en) *	2006-05-12	2007-11-22	Unilever N.V.	Aqueous liquid cleaning compositions and their use
FR2954107B1 (fr)	2009-12-23	2012-04-20	Oreal	Composition cosmetique sous forme de nanoemulsion contenant un alcane lineaire volatil
US9168218B2 (en)	2011-01-25	2015-10-27	L'oreal S.A.	Use of photoluminescent polymers in cosmetic products
US20140186411A1 (en)	2012-12-27	2014-07-03	L'oreal	Low viscosity meta-stable photoprotection composition
US9433578B2 (en)	2013-05-17	2016-09-06	L'oreal	Stable bubbles via particle absorption by electrostatic interaction
WO2014184660A2 (en)	2013-05-17	2014-11-20	L'oreal	Emulsion stabilization
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
EP3075436B1 (de) *	2015-04-02	2018-08-01	Afton Chemical Limited	Diesel-exhaust-fluid-lösungen und verfahren zur verwendung davon

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US3045042A (en) *	1957-08-16	1962-07-17	Monsanto Chemicals	Acid polyester succinates
US3002064A (en) *	1958-03-26	1961-09-26	Axel L Nielsen	Sump pump and flood control equipment
DE1570888A1 (de) *	1963-08-29	1970-03-19	Monsanto Co	Verfahren zur Herstellen eines oberflaechenaktiven Agens
US3821069A (en) *	1973-01-02	1974-06-28	Nat Starch Chem Corp	Process of sizing paper with a reaction product of maleic anhydride and an internal olefin
US3968310A (en) *	1974-03-14	1976-07-06	A. E. Staley Manufacturing Company	Half-ester reaction products of maleated alpha-olefins and monohydric alcohols
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DE2963798D1 (en) *	1978-03-23	1982-11-11	Ici Plc	Surfactant compositions comprising a blend of two types of polyester and an emulsion of oil in water prepared therewith
JPS5947498A (ja) *	1982-09-06	1984-03-17	星光化学工業株式会社	置換コハク酸無水物の水分散性組成物

1983
- 1983-12-02 IL IL70368A patent/IL70368A/xx not_active IP Right Cessation
- 1983-12-09 NL NL8304253A patent/NL8304253A/nl not_active Application Discontinuation
- 1983-12-09 SE SE8306812A patent/SE459789B/sv not_active IP Right Cessation
- 1983-12-12 GB GB08333102A patent/GB2131820B/en not_active Expired
- 1983-12-13 BE BE0/212035A patent/BE898441A/fr not_active IP Right Cessation
- 1983-12-13 DE DE19833345058 patent/DE3345058A1/de not_active Withdrawn
- 1983-12-13 FR FR838319930A patent/FR2537454B1/fr not_active Expired - Fee Related
- 1983-12-13 JP JP58234918A patent/JPS59115733A/ja active Pending

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US5872149A (en) *	1995-02-15	1999-02-16	Basf Aktiengesellschaft	Alk(en)yldicarboxylic acid bisesters, their use, and processes for their preparation

Also Published As

Publication number	Publication date
GB2131820B (en)	1986-09-10
IL70368A0 (en)	1984-03-30
SE8306812L (sv)	1984-06-14
SE8306812D0 (sv)	1983-12-09
IL70368A (en)	1987-11-30
GB8333102D0 (en)	1984-01-18
JPS59115733A (ja)	1984-07-04
FR2537454B1 (fr)	1990-02-02
FR2537454A1 (fr)	1984-06-15
DE3345058A1 (de)	1984-06-14
SE459789B (sv)	1989-08-07
GB2131820A (en)	1984-06-27
NL8304253A (nl)	1984-07-02

Legal Events

Date

Code

Title

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1995-06-30

RE

Patent lapsed

Owner name: CHEVRON RESEARCH CY

Effective date: 19941231

Publication	Publication Date	Title
BE898441A (fr)	1984-03-30	Emulsionnant non ionique et compositions d'un anhydride succinique substitué avec cet émulsionnant.
US4915786A (en)	1990-04-10	Nonionic emulsifier and substituted succinic anhydride compositons therewith
FR2543563A1 (fr)	1984-10-05	Composition a base d'un anhydride succinique substitue et d'un emulsionnant et son application au collage du papier
FR2482092A1 (fr)	1981-11-13	Compose d'ammonium quaternaire tensioactif adapte pour le traitement de matieres a base de textile et de cellulose
EP0282415A1 (de)	1988-09-14	Verfahren zur Papierherstellung
DE2460262A1 (de)	1975-07-03	N-acylierte cyclische imide, verfahren zu ihrer herstellung und die verbindungen enthaltende mittel
US4111650A (en)	1978-09-05	Stable concentrated liquid preparation of a paper dye of the copper phthalocyanine class
BE1006004A4 (fr)	1994-04-19	Composition de colorants rouges reactifs pour fibres.
FR2560066A1 (fr)	1985-08-30	Composition stable contenant un anhydride succinique substitue et un emulsionnant et son procede d'utilisation
FR2606047A1 (fr)	1988-05-06	Agent d'encollage du type emulsion de resine
US4695401A (en)	1987-09-22	Nonionic emulsifier and substituted succinic anhydride compositions therewith
FR2554013A1 (fr)	1985-05-03	Emulsionnant stable a groupe polyethylene-oxy et composition d'anhydride succinique substitue le contenant
BE446643A (de)	1900-01-01
EP0232196B1 (de)	1989-09-13	Diurethan-Latex als Leimungsmittel in der Papierindustrie und dessen Herstellungsverfahren
CH630660A5 (en)	1982-06-30	Inversion process for the preparation of papermaking glue from reinforced rosin
US20230250197A1 (en)	2023-08-10	Oxidized cellulose, nanocellulose, and their dispersions
Reinhardt et al.	1966	Carboxyethylation of cotton by treatment with acrylamide
SU670654A1 (ru)	1979-06-30	Состав дл обессмоливани целлюлозы
US653411A (en)	1900-07-10	Process of making tobacco-brown wrapping-paper.
US414351A (en)	1889-11-05	Joseph warren wattles
RU2065489C1 (ru)	1996-08-20	Способ получения твердого мыла
US1402553A (en)	1922-01-03	Wood stain and process of making same
BE644902A (de)	1964-07-01
RU2334037C1 (ru)	2008-09-20	Состав для гидрофобизации целлюлозных материалов
BE675501A (de)	1966-05-16

BE898441A - Emulsionnant non ionique et compositions d'un anhydride succinique substitué avec cet émulsionnant. - Google Patents

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