CA1050384A - Aluminosilicates contenant des agents tensio-actifs - Google Patents

Aluminosilicates contenant des agents tensio-actifs

Info

Publication number: CA1050384A
Authority: CA; Canada
Prior art keywords: water; aluminosilicates; mols; sio2; composition
Prior art date: 1973-09-07
Legal status (The legal status 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 status listed.): Expired

Application number

CA208,785A

Other languages

English (en)

Other versions

CA208785S (en

Inventor

Milan J. Schwuger

Elmar Reinwald

Heinz Smolka

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Henkel AG and Co KGaA

Evonik Operations GmbH

Original Assignee

Henkel AG and Co KGaA

Deutsche Gold und Silber Scheideanstalt

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.)

1973-09-07

Filing date

1974-09-09

Publication date

1979-03-13

1973-09-07 Priority claimed from AT777173A external-priority patent/AT330100B/de

1973-10-01 Priority claimed from AT838273A external-priority patent/AT330101B/de

1973-12-03 Priority claimed from AT1009873A external-priority patent/AT330102B/de

1974-09-09 Application filed by Henkel AG and Co KGaA, Deutsche Gold und Silber Scheideanstalt filed Critical Henkel AG and Co KGaA

1977-06-30 Priority claimed from US05/811,964 external-priority patent/US4126574A/en

1979-03-13 Application granted granted Critical

1979-03-13 Publication of CA1050384A publication Critical patent/CA1050384A/fr

Status Expired legal-status Critical Current

Links

229910000323 aluminium silicate Inorganic materials 0.000 title claims abstract description 46
239000004094 surface-active agent Substances 0.000 title claims abstract description 33
238000000034 method Methods 0.000 title claims abstract description 13
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 103
229910001868 water Inorganic materials 0.000 claims abstract description 95
238000001556 precipitation Methods 0.000 claims abstract description 83
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 80
229910052681 coesite Inorganic materials 0.000 claims abstract description 54
229910052906 cristobalite Inorganic materials 0.000 claims abstract description 54
229910052682 stishovite Inorganic materials 0.000 claims abstract description 54
229910052905 tridymite Inorganic materials 0.000 claims abstract description 54
235000012239 silicon dioxide Nutrition 0.000 claims abstract description 50
239000000377 silicon dioxide Substances 0.000 claims abstract description 49
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims abstract description 19
239000007864 aqueous solution Substances 0.000 claims abstract description 14
150000001768 cations Chemical group 0.000 claims abstract description 11
238000006243 chemical reaction Methods 0.000 claims abstract description 11
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 5
238000002360 preparation method Methods 0.000 claims abstract description 5
229910052593 corundum Inorganic materials 0.000 claims abstract 4
229910001845 yogo sapphire Inorganic materials 0.000 claims abstract 4
239000000243 solution Substances 0.000 claims description 52
239000000725 suspension Substances 0.000 claims description 50
150000001875 compounds Chemical class 0.000 claims description 33
125000002091 cationic group Chemical group 0.000 claims description 28
239000011734 sodium Substances 0.000 claims description 9
150000004645 aluminates Chemical class 0.000 claims description 8
239000004753 textile Substances 0.000 claims description 8
238000005406 washing Methods 0.000 claims description 8
239000002245 particle Substances 0.000 claims description 7
229910052708 sodium Inorganic materials 0.000 claims description 7
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 claims description 5
239000011575 calcium Substances 0.000 claims description 5
229910001415 sodium ion Inorganic materials 0.000 claims description 5
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 4
229910052791 calcium Inorganic materials 0.000 claims description 4
239000013543 active substance Substances 0.000 claims description 3
230000014759 maintenance of location Effects 0.000 claims description 3
150000004760 silicates Chemical class 0.000 claims description 3
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 2
229910052744 lithium Inorganic materials 0.000 claims description 2
239000004902 Softening Agent Substances 0.000 claims 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical group [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 claims 1
239000008346 aqueous phase Substances 0.000 claims 1
239000007900 aqueous suspension Substances 0.000 claims 1
229910052700 potassium Inorganic materials 0.000 claims 1
239000011591 potassium Substances 0.000 claims 1
239000002689 soil Substances 0.000 claims 1
230000000153 supplemental effect Effects 0.000 claims 1
101100208039 Rattus norvegicus Trpv5 gene Proteins 0.000 abstract description 5
238000002425 crystallisation Methods 0.000 abstract 1
230000008025 crystallization Effects 0.000 abstract 1
230000009919 sequestration Effects 0.000 abstract 1
239000000203 mixture Substances 0.000 description 85
239000000047 product Substances 0.000 description 83
KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 67
239000007787 solid Substances 0.000 description 40
ASRSBXRMOCLKQC-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)-n-methoxyacetamide Chemical compound CONC(=O)COC1=CC=C(Cl)C=C1C ASRSBXRMOCLKQC-UHFFFAOYSA-N 0.000 description 22
239000002253 acid Substances 0.000 description 22
239000008367 deionised water Substances 0.000 description 16
229910021641 deionized water Inorganic materials 0.000 description 16
125000004432 carbon atom Chemical group C* 0.000 description 15
125000000217 alkyl group Chemical group 0.000 description 14
239000003093 cationic surfactant Substances 0.000 description 14
125000000129 anionic group Chemical group 0.000 description 12
229960003237 betaine Drugs 0.000 description 12
KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 11
KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 11
150000002500 ions Chemical class 0.000 description 10
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 9
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 9
229910001388 sodium aluminate Inorganic materials 0.000 description 9
150000007513 acids Chemical class 0.000 description 8
-1 alkyl gro Chemical compound 0.000 description 8
239000003240 coconut oil Substances 0.000 description 8
235000019864 coconut oil Nutrition 0.000 description 8
238000012360 testing method Methods 0.000 description 8
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
235000019589 hardness Nutrition 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
125000004429 atom Chemical group 0.000 description 6
230000000052 comparative effect Effects 0.000 description 6
238000003756 stirring Methods 0.000 description 6
239000003760 tallow Substances 0.000 description 6
239000004215 Carbon black (E152) Substances 0.000 description 5
229910052799 carbon Inorganic materials 0.000 description 5
238000009472 formulation Methods 0.000 description 5
125000005842 heteroatom Chemical group 0.000 description 5
229930195733 hydrocarbon Natural products 0.000 description 5
150000002430 hydrocarbons Chemical class 0.000 description 5
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 5
239000000126 substance Substances 0.000 description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
229910000503 Na-aluminosilicate Inorganic materials 0.000 description 4
239000004115 Sodium Silicate Substances 0.000 description 4
125000001931 aliphatic group Chemical group 0.000 description 4
150000001721 carbon Chemical group 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
239000012452 mother liquor Substances 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
235000012217 sodium aluminium silicate Nutrition 0.000 description 4
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical class [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 4
229910052911 sodium silicate Inorganic materials 0.000 description 4
235000013162 Cocos nucifera Nutrition 0.000 description 3
244000060011 Cocos nucifera Species 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
241000219146 Gossypium Species 0.000 description 3
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
150000004996 alkyl benzenes Chemical class 0.000 description 3
239000002585 base Substances 0.000 description 3
238000005341 cation exchange Methods 0.000 description 3
239000007859 condensation product Substances 0.000 description 3
230000002209 hydrophobic effect Effects 0.000 description 3
239000007788 liquid Substances 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
125000004433 nitrogen atom Chemical group N* 0.000 description 3
239000000429 sodium aluminium silicate Substances 0.000 description 3
229910052938 sodium sulfate Inorganic materials 0.000 description 3
235000011152 sodium sulphate Nutrition 0.000 description 3
238000000967 suction filtration Methods 0.000 description 3
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 3
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
241000282326 Felis catus Species 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
239000007832 Na2SO4 Substances 0.000 description 2
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
150000001335 aliphatic alkanes Chemical class 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
229940037003 alum Drugs 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
239000000306 component Substances 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
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 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
125000001188 haloalkyl group Chemical group 0.000 description 2
125000001165 hydrophobic group Chemical group 0.000 description 2
239000002563 ionic surfactant Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
CXHHBNMLPJOKQD-UHFFFAOYSA-N methyl hydrogen carbonate Chemical class COC(O)=O CXHHBNMLPJOKQD-UHFFFAOYSA-N 0.000 description 2
APVPOHHVBBYQAV-UHFFFAOYSA-N n-(4-aminophenyl)sulfonyloctadecanamide Chemical class CCCCCCCCCCCCCCCCCC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 APVPOHHVBBYQAV-UHFFFAOYSA-N 0.000 description 2
MJCJUDJQDGGKOX-UHFFFAOYSA-N n-dodecyldodecan-1-amine Chemical compound CCCCCCCCCCCCNCCCCCCCCCCCC MJCJUDJQDGGKOX-UHFFFAOYSA-N 0.000 description 2
IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 2
229940055577 oleyl alcohol Drugs 0.000 description 2
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 2
125000000913 palmityl 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])([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 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
235000014786 phosphorus Nutrition 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
125000001453 quaternary ammonium group Chemical group 0.000 description 2
239000011347 resin Substances 0.000 description 2
229920005989 resin Polymers 0.000 description 2
IOVGROKTTNBUGK-SJCJKPOMSA-N ritodrine Chemical compound N([C@@H](C)[C@H](O)C=1C=CC(O)=CC=1)CCC1=CC=C(O)C=C1 IOVGROKTTNBUGK-SJCJKPOMSA-N 0.000 description 2
239000013049 sediment Substances 0.000 description 2
229910000144 sodium(I) superoxide Inorganic materials 0.000 description 2
238000006277 sulfonation reaction Methods 0.000 description 2
150000008053 sultones Chemical class 0.000 description 2
150000003512 tertiary amines Chemical class 0.000 description 2
238000004448 titration Methods 0.000 description 2
239000002888 zwitterionic surfactant Substances 0.000 description 2
IGWBMTVWNGMSRK-UHFFFAOYSA-M (1,6-dimethylcyclohexa-2,4-dien-1-yl)methyl-dodecyl-dimethylazanium;bromide Chemical compound [Br-].CCCCCCCCCCCC[N+](C)(C)CC1(C)C=CC=CC1C IGWBMTVWNGMSRK-UHFFFAOYSA-M 0.000 description 1
PSBDWGZCVUAZQS-UHFFFAOYSA-N (dimethylsulfonio)acetate Chemical compound C[S+](C)CC([O-])=O PSBDWGZCVUAZQS-UHFFFAOYSA-N 0.000 description 1
QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 1
GKQHIYSTBXDYNQ-UHFFFAOYSA-M 1-dodecylpyridin-1-ium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+]1=CC=CC=C1 GKQHIYSTBXDYNQ-UHFFFAOYSA-M 0.000 description 1
ZILVNHNSYBNLSZ-UHFFFAOYSA-N 2-(diaminomethylideneamino)guanidine Chemical compound NC(N)=NNC(N)=N ZILVNHNSYBNLSZ-UHFFFAOYSA-N 0.000 description 1
ZMPRRFPMMJQXPP-UHFFFAOYSA-N 2-sulfobenzoic acid Chemical compound OC(=O)C1=CC=CC=C1S(O)(=O)=O ZMPRRFPMMJQXPP-UHFFFAOYSA-N 0.000 description 1
XPYQFIISZQCINN-QVXDJYSKSA-N 4-amino-1-[(2r,3e,4s,5r)-3-(fluoromethylidene)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one;hydrate Chemical compound O.O=C1N=C(N)C=CN1[C@H]1C(=C/F)/[C@H](O)[C@@H](CO)O1 XPYQFIISZQCINN-QVXDJYSKSA-N 0.000 description 1
101150034533 ATIC gene Proteins 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
101100087530 Caenorhabditis elegans rom-1 gene Proteins 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
241000861718 Chloris <Aves> Species 0.000 description 1
101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 1
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 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
101100384355 Mus musculus Ctnnbip1 gene Proteins 0.000 description 1
101100305983 Mus musculus Rom1 gene Proteins 0.000 description 1
DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical group NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 1
241000047703 Nonion Species 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
235000014676 Phragmites communis Nutrition 0.000 description 1
239000004721 Polyphenylene oxide Chemical group 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
241000950638 Symphysodon discus Species 0.000 description 1
TVWHNULVHGKJHS-UHFFFAOYSA-N Uric acid Natural products N1C(=O)NC(=O)C2NC(=O)NC21 TVWHNULVHGKJHS-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
230000002730 additional effect Effects 0.000 description 1
239000000654 additive Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
229910052910 alkali metal silicate Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
229910021502 aluminium hydroxide Inorganic materials 0.000 description 1
125000003368 amide group Chemical group 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
230000000845 anti-microbial effect Effects 0.000 description 1
DQSGVVGOPRWTKI-QVFAWCHISA-N atazanavir sulfate Chemical compound [H+].[H+].[O-]S([O-])(=O)=O.C([C@H](NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1N=CC=CC=1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C1=CC=CC=C1 DQSGVVGOPRWTKI-QVFAWCHISA-N 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
229940077388 benzenesulfonate Drugs 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
210000001217 buttock Anatomy 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 1
RLGQACBPNDBWTB-UHFFFAOYSA-N cetyltrimethylammonium ion Chemical group CCCCCCCCCCCCCCCC[N+](C)(C)C RLGQACBPNDBWTB-UHFFFAOYSA-N 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
229940106681 chloroacetic acid Drugs 0.000 description 1
125000004803 chlorobenzyl group Chemical group 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000013270 controlled release Methods 0.000 description 1
239000012043 crude product Substances 0.000 description 1
238000000151 deposition Methods 0.000 description 1
238000011161 development Methods 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
229940043237 diethanolamine Drugs 0.000 description 1
MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 description 1
IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
HWYQLDHDBPXEQU-UHFFFAOYSA-M dodecoxymethyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCOC[N+](C)(C)C HWYQLDHDBPXEQU-UHFFFAOYSA-M 0.000 description 1
DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 1
VICYBMUVWHJEFT-UHFFFAOYSA-N dodecyltrimethylammonium ion Chemical compound CCCCCCCCCCCC[N+](C)(C)C VICYBMUVWHJEFT-UHFFFAOYSA-N 0.000 description 1
XWBDWHCCBGMXKG-UHFFFAOYSA-N ethanamine;hydron;chloride Chemical compound Cl.CCN XWBDWHCCBGMXKG-UHFFFAOYSA-N 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
238000007046 ethoxylation reaction Methods 0.000 description 1
WBJINCZRORDGAQ-UHFFFAOYSA-N ethyl formate Chemical compound CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000003925 fat Substances 0.000 description 1
235000019197 fats Nutrition 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
229910001679 gibbsite Inorganic materials 0.000 description 1
150000003977 halocarboxylic acids Chemical class 0.000 description 1
239000008233 hard water Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
150000002466 imines Chemical class 0.000 description 1
229910052610 inosilicate Inorganic materials 0.000 description 1
238000005342 ion exchange Methods 0.000 description 1
210000005053 lamin Anatomy 0.000 description 1
HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
229910052919 magnesium silicate Inorganic materials 0.000 description 1
235000019792 magnesium silicate Nutrition 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
150000005673 monoalkenes Chemical class 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
HTKPDYSCAPSXIR-UHFFFAOYSA-N octyltrimethylammonium ion Chemical group CCCCCCCC[N+](C)(C)C HTKPDYSCAPSXIR-UHFFFAOYSA-N 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
210000000056 organ Anatomy 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
125000001477 organic nitrogen group Chemical group 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
239000003346 palm kernel oil Substances 0.000 description 1
235000019865 palm kernel oil Nutrition 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 1
HCTVWSOKIJULET-LQDWTQKMSA-M phenoxymethylpenicillin potassium Chemical compound [K+].N([C@H]1[C@H]2SC([C@@H](N2C1=O)C([O-])=O)(C)C)C(=O)COC1=CC=CC=C1 HCTVWSOKIJULET-LQDWTQKMSA-M 0.000 description 1
UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000570 polyether Chemical group 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
235000019353 potassium silicate Nutrition 0.000 description 1
150000003138 primary alcohols Chemical class 0.000 description 1
239000001294 propane Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000003333 secondary alcohols Chemical class 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
229910052814 silicon oxide Inorganic materials 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000001509 sodium citrate Substances 0.000 description 1
NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
229960001922 sodium perborate Drugs 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
235000019832 sodium triphosphate Nutrition 0.000 description 1
YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
238000001179 sorption measurement Methods 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
125000004079 stearyl 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])([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])[H] 0.000 description 1
229940117986 sulfobetaine Drugs 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
235000012976 tarts Nutrition 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
125000005425 toluyl group Chemical group 0.000 description 1
238000011282 treatment Methods 0.000 description 1
PDSVZUAJOIQXRK-UHFFFAOYSA-N trimethyl(octadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)C PDSVZUAJOIQXRK-UHFFFAOYSA-N 0.000 description 1
229940116269 uric acid Drugs 0.000 description 1
150000007968 uric acids Chemical class 0.000 description 1

Landscapes

Detergent Compositions (AREA)

CA208,785A 1973-09-07 1974-09-09 Aluminosilicates contenant des agents tensio-actifs Expired CA1050384A (fr)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
AT777173A AT330100B (de)	1973-09-07	1973-09-07	Verfahren zur herstellung neuer, rontgenamorpher, kationaustauschender, gegebenenfalls gebundenes wasser enthaltender aluminiumsilikate
AT838273A AT330101B (de)	1973-10-01	1973-10-01	Verfahren zur herstellung neuer, rontgenamorpher, kationaustauschender, gegebenenfalls gebundenes wasser enthaltender aluminiumsilikate
AT1009873A AT330102B (de)	1973-12-03	1973-12-03	Verfahren zur herstellung neuer, rontgenamorpher, kationaustauschender, gegebenenfalls gebundenes wasser enthaltender aluminiumsilikate
US05/811,964 US4126574A (en)	1973-09-07	1977-06-30	Surfactant-containing aluminosilicates and process

Publications (1)

Publication Number	Publication Date
CA1050384A true CA1050384A (fr)	1979-03-13

Family

ID=27422232

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA208,785A Expired CA1050384A (fr)	1973-09-07	1974-09-09	Aluminosilicates contenant des agents tensio-actifs

Country Status (1)

Country	Link
CA (1)	CA1050384A (fr)

1974
- 1974-09-09 CA CA208,785A patent/CA1050384A/fr not_active Expired

Publication	Publication Date	Title
US4126574A (en)	1978-11-21	Surfactant-containing aluminosilicates and process
CA1062984A (fr)	1979-09-25	Suspensions aqueuses stables d'aluminosilicates insolubles dans l'eau, retenant le calcium, et d'agents de suspension organiques
DE69516182T2 (de)	2000-08-17	Aminonitrile zwischenprodukte zur herstellung von alamindiessigsaüre
CA1230206A (fr)	1987-12-15	Detergent renfermant un assouplisseur
DE68918561T2 (de)	1995-01-26	Bleichzusammensetzung.
CA1178383A (fr)	1984-11-20	Sequestration de ca su xx et de mg su xx dans des milieux aqueux a l'aide de melanges de zeolite
DE68901737T2 (de)	1993-02-04	Alkylsulphonylpercarbonsaeuren und die sie enthaltenden bleichmittel- und reinigungszusammensetzungen.
US4201689A (en)	1980-05-06	Process for the production of tenside-containing cation exchanger aluminosilicates
CA1251440A (fr)	1989-03-21	Adsorbants a base d'acides phyllosiliciques, modifies pour etre organophiliques
US6274111B1 (en)	2001-08-14	Synthetic magnesium silicate
EP0087035B1 (fr)	1985-09-11	Compositions détergentes contenant du zéolithe et procédé pour leur préparation
CH630322A5 (de)	1982-06-15	Stabile suspensionen wasserunloeslicher, zum binden von calciumionen befaehigter silikate und deren verwendung zur herstellung von wasch- und reinigungsmitteln.
US2174506A (en)	1939-09-26	Process of reacting alicyclic hydrocarbons with chlorine and sulphur dioxide and products thereof
CA1050384A (fr)	1979-03-13	Aluminosilicates contenant des agents tensio-actifs
JPS6052195B2 (ja)	1985-11-18	液状からペ−スト状までの濃厚洗剤及び清浄剤
DE68928767T3 (de)	2002-05-08	Imido-percarbonsäuren
EP0015366A2 (fr)	1980-09-17	Procédé de préparation de solutions aqueuses d'organosiliconates de métaux alcalins
JPS5833917B2 (ja)	1983-07-22	繊維を洗浄及び漂白する方法
DE69616085T2 (de)	2002-03-14	Aminonitril-zwischenprodukte zur herstellung von 2-hydroxyethyliminodiessigsäure
US2265944A (en)	1941-12-09	Amidine salts of sulphosuccinic esters
FI66130C (fi)	1984-09-10	Syntetiskt finfoerdelat kristallint silikonaluminat foerfarande foer dess framstaellning samt dess anvaendning
JPH0249299B2 (fr)	1990-10-29
DE2330436A1 (de)	1975-01-09	Verwendung von im wesentlichen carboxymethylpolyglykolaether enthaltenden stoffgemischen als vergrauungsinhibitor in waschund reinigungsmitteln
SU983045A1 (ru)	1982-12-23	Способ фильтровани кремнеземсодержащих суспензий
CH624914A5 (en)	1981-08-31	Process for preparing cation-exchanging alkali metal alumosilicates