MXPA00003481A - Highly alkaline compositions containing a hexyl glycoside as a hydrotrope - Google Patents
Highly alkaline compositions containing a hexyl glycoside as a hydrotropeInfo
- Publication number
- MXPA00003481A MXPA00003481A MXPA/A/2000/003481A MXPA00003481A MXPA00003481A MX PA00003481 A MXPA00003481 A MX PA00003481A MX PA00003481 A MXPA00003481 A MX PA00003481A MX PA00003481 A MXPA00003481 A MX PA00003481A
- Authority
- MX
- Mexico
- Prior art keywords
- group
- carbon atoms
- alkaline
- glycoside
- cleaning
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 57
- -1 hexyl glycoside Chemical class 0.000 title claims abstract description 41
- 229930182470 glycoside Natural products 0.000 title claims abstract description 33
- 239000003752 hydrotrope Substances 0.000 title claims abstract description 19
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 title claims abstract description 13
- 238000004140 cleaning Methods 0.000 claims abstract description 26
- 238000000034 method Methods 0.000 claims abstract description 17
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 10
- 238000009991 scouring Methods 0.000 claims abstract description 10
- 238000005517 mercerization Methods 0.000 claims abstract description 8
- 239000004744 fabric Substances 0.000 claims abstract description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 20
- 239000002736 nonionic surfactant Substances 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 9
- 239000000835 fiber Substances 0.000 claims description 7
- 239000008139 complexing agent Substances 0.000 claims description 6
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 125000002252 acyl group Chemical group 0.000 claims description 4
- 150000002338 glycosides Chemical class 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000005529 alkyleneoxy group Chemical group 0.000 claims description 3
- 125000001483 monosaccharide substituent group Chemical group 0.000 claims 1
- 125000000963 oxybis(methylene) group Chemical group [H]C([H])(*)OC([H])([H])* 0.000 claims 1
- 238000009736 wetting Methods 0.000 abstract description 12
- 238000009990 desizing Methods 0.000 abstract description 4
- 238000005187 foaming Methods 0.000 abstract description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 17
- 239000000243 solution Substances 0.000 description 17
- 229930182478 glucoside Natural products 0.000 description 12
- 239000004094 surface-active agent Substances 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- 239000006260 foam Substances 0.000 description 11
- 238000009472 formulation Methods 0.000 description 10
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 9
- 239000012141 concentrate Substances 0.000 description 8
- 239000007788 liquid Substances 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 235000011121 sodium hydroxide Nutrition 0.000 description 5
- 239000000080 wetting agent Substances 0.000 description 5
- 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 4
- 239000003599 detergent Substances 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- JDRSMPFHFNXQRB-CMTNHCDUSA-N Decyl beta-D-threo-hexopyranoside Chemical compound CCCCCCCCCCO[C@@H]1O[C@H](CO)C(O)[C@H](O)C1O JDRSMPFHFNXQRB-CMTNHCDUSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 239000012670 alkaline solution Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229940073499 decyl glucoside Drugs 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 238000005063 solubilization Methods 0.000 description 3
- 230000007928 solubilization Effects 0.000 description 3
- JBVOQKNLGSOPNZ-UHFFFAOYSA-N 2-propan-2-ylbenzenesulfonic acid Chemical compound CC(C)C1=CC=CC=C1S(O)(=O)=O JBVOQKNLGSOPNZ-UHFFFAOYSA-N 0.000 description 2
- 241000004297 Draba Species 0.000 description 2
- 229910019142 PO4 Chemical class 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 2
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000012459 cleaning agent Substances 0.000 description 2
- 229940071118 cumenesulfonate Drugs 0.000 description 2
- 230000000994 depressogenic effect Effects 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 229940048842 sodium xylenesulfonate Drugs 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 1
- JVAZJLFFSJARQM-RMPHRYRLSA-N (2r,3r,4s,5s,6r)-2-hexoxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound CCCCCCO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O JVAZJLFFSJARQM-RMPHRYRLSA-N 0.000 description 1
- BZANQLIRVMZFOS-ZKZCYXTQSA-N (3r,4s,5s,6r)-2-butoxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound CCCCOC1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O BZANQLIRVMZFOS-ZKZCYXTQSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004435 Oxo alcohol Substances 0.000 description 1
- 206010033546 Pallor Diseases 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000006065 biodegradation reaction Methods 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000004590 computer program Methods 0.000 description 1
- 230000000254 damaging effect Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 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
- 239000007857 degradation product Substances 0.000 description 1
- 238000011033 desalting Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 229960004756 ethanol Drugs 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- CBCIHIVRDWLAME-UHFFFAOYSA-N hexanitrodiphenylamine Chemical class [O-][N+](=O)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1NC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O CBCIHIVRDWLAME-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 229910021432 inorganic complex Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000006101 laboratory sample Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 150000002772 monosaccharides Chemical group 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- LQPLDXQVILYOOL-UHFFFAOYSA-I pentasodium;2-[bis[2-[bis(carboxylatomethyl)amino]ethyl]amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC(=O)[O-])CCN(CC([O-])=O)CC([O-])=O LQPLDXQVILYOOL-UHFFFAOYSA-I 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000004758 synthetic textile Substances 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- YBAPEZRVAJFQCN-UHFFFAOYSA-J tetrasodium;2-[3-[bis(carboxylatomethyl)amino]propyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCCN(CC([O-])=O)CC([O-])=O YBAPEZRVAJFQCN-UHFFFAOYSA-J 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Abstract
The present invention relates to a clear and stable, highly alkaline composition with controlled foaming, containing a high amount of surface active nonionic alkylene oxide adduct and a hexyl glycoside as a hydrotrope. This composition has a very good wetting and cleaning ability and can be used for cleaning of hard surfaces, in a mercerization process and for a cleaning, desizing or scouring process of fibres and fabrics.
Description
HIGHLY ALKALINE COMPOSITIONS CONTAINING A HEXYL GLICOSIDE LIKE A HYDROTHROP
DESCRIPTION OF THE INVENTION
The present invention relates to a clear and stable, highly alkaline composition with controlled foaming, which contains a high amount of nonionic, surface active alkylene oxide adduct, and a hexyl glycoside as a hydrotrope. This composition has a very good wetting and cleaning ability and can be used to clean hard surfaces, in a mercerization process, and for a process of cleaning, desizing or scouring of fibers and fabrics. Highly alkaline compositions, such as concentrates having a high content of alkaline agents, such as alkali hydroxides, alkaline complexing agents and silicates, and having a pH value above 11, preferably above 13, are frequently used for cleaning hard surfaces, mercerizing, scouring, etc. A good wetting ability combined with a good cleaning effect is essential in the aforementioned applications, which requires the presence of considerable amounts of suitable surfactants to decrease the high surface tension caused by the high amount of electrolytes. It is also important to have a controlled foam formation in these systems. To minimize the cost of transportation, these concentrates should contain quantities of water and other solvents as small as possible. It is also advantageous if the concentrates remain homogeneous during transportation and storage. Since these compositions contain high amounts of electrolytes, such as complexing agents with alkali and / or alkali metal, it is difficult to dissolve large amounts of surfactants, especially nonionic surfactants. Therefore, in order to improve solubility, hydrotropes are frequently added, and the most commonly used hydrotropes are ethanol and sodium xylene or cumene sulfonate. Ethanol is rather efficient, but presents an explosion hazard, and sodium xylene or cumene sulfonate is relatively inefficient at higher levels of surfactant.
If a surfactant that is soluble in aqueous alkaline solutions is used without the addition of a hydrotrope, there will be a problem with too much foam, which requires the addition of a foam depressant. Alkyl glycosides have previously been used in highly alkaline compositions, see for example EP-B1-589,978, EP-A1-638, 685 and US-4, 240, 921. In addition, alkyl glycosides are well known as cleaning agents active in cleaning compositions commonly used, see for example WO 97/34971, US-4,627,931 and EP-B1-075, 995. European Patent EP-B1-589, 978 describes the use of alkyl glycosides of 8 to 14 carbon atoms as surface active auxiliaries in the desalting, bleaching and alkaline scouring of sheet-like, natural and / or synthetic textile materials, threads or fluffs, while European Patent EP-Al-638, 685 refers to a mercerization wetting agent containing, either alone or in combination, an alkyl glycoside of 4 to 18 carbon atoms, an alkyl glycine amide of 4 to 18 carbon atoms and the corresponding sulfonated derivatives. Highly alkaline, liquid-containing cleaning liquids containing an alkyl glycoside or an alkyl glycidyl ether and non-ionic alkylene oxide adducts are described in US Pat. No. 4,240,921. Preferred alkylene oxide adducts are those capable of acting as foam depressants, such as polyoxyethylene / polyoxypropylene block copolymers and cased alcohol ethoxylates. The concentrate contains: a) 10 to 35% by weight of alkali metal hydroxide b) 10 to 50% by weight of a mixture of a first nonionic surfactant which is a polyoxypropylene-polyoxyethylene condense which acts as a foam depressant, and a second nonionic surfactant which is a casted ethoxylated alcohol, together with an alkyl glycoside or an alkyl glycidyl ether, where the weight ratio between the alkyl glycoside or the glycidyl alkyl ether and the first and second surfactants non-ionic aforementioned, is between 5: 1 to 10: 1 and c) the rest of water. These concentrates are used to formulate low foaming cleaning compositions which are useful for example in the food industry. However, the above composition described in US Patent No. 4,240,921 requires a rather high proportion of alkyl glycoside to the other nonionic surfactants present in the composition. Furthermore, it is well known that the inclusion of larger amounts of PO in an alkoxylate, such as in the foam depressants of the Pluronic type, has a negative influence on the biodegradation capacity of the product. Finally, a cased alcohol ethoxylate is usually a poor wetting agent and also has a low cleaning ability. Their presence also increases the need for an extra amount of the alkyl glycoside or the glycidyl alkyl ether. There is consequently a need for highly alkaline compositions with improved properties. It has now been found that highly alkaline compositions have a pH above 11, preferably at least 13 and more preferably above 13.7, which show excellent cleansing and wetting ability, can be prepared by the use of a glycoside of hexyl that has the formula
CßHiaOGn (I
where G is a monosaccharide residue and n is from 1 to 5, as a hydrotrope for a surface active nonionic alkylene oxide adduct that is insoluble in the highly alkaline composition and contains a hydrocarbon group or an acyl group of 8 to 24 carbon atoms and at least one primary hydroxyl group in the alkoxylated part of the molecule. Suitably, the adduct has the formula
R (AO) x (C2H40) and H (II)
where R is an alkoxy group R 'O- having from 8 to 24 carbon atoms or a group R "' CONR '' ', where R" is a hydrocarbon group having 7 to 23 carbon atoms, R' '' is hydrogen or a group - (AO) x (C2H40) and H, preferably hydrogen, AO is an alkyleneoxy group having 2 to 4 carbon atoms, x is a number from 0 to 5 and y is a number from 1 to 10.
The present invention also relates to a composition having a pH value above 11, which contains a) from 3 to 50% by weight of alkali metal hydroxide and / or complexing agents, alkaline, b) of 0.05 to 30% by weight of an adduct of nonionic alkylene oxide, active surface, having a hydrocarbon group or an acyl group of 8 to 24 carbon atoms and having at least one primary hydroxyl group in the alkoxylated part of the molecule, c) from 0.04 to 30% by weight of a hexyl glycoside, and d) from 20 to 97% by weight of water. The proportion by weight between the hexyl glycoside and the surfactant according to formula II is from 1:10 to 10: 1, preferably from 1:10 to 4: 1. It should be noted that the alkyl glucosides have been used in less alkaline detergent compositions, where the conditions are different. Examples of such compositions are to be found in U.S. Patent No. 4,488.91 and European Patent EP-B1- 136, 844.
U.S. Patent No. 4,488,981 and European Patent EP-B1-136, 844 describe the use of the alkyl glycosides of 2 to 6 carbon atoms to reduce the viscosity and prevent phase separation in an aqueous liquid detergent, for example in liquid shampoos and soaps and in heavy-duty liquids. The alkyl glycosides of 2 to 4 carbon atoms are the most preferred alkyl glycosides, since these are more effective in reducing viscosity. In addition, US Patent No. 5,525,256 and Statutory Invention H 468 disclose liquid, alkaline, industrial and institutional cleaning compositions containing alkyl glycosides of 8 to 25 carbon atoms as cleaning agents. However, none of these references describe the unexpected effects of hexyl glycosides in highly alkaline cleaning compositions, containing at least 3%, preferably at least 20% alkaline and / or alkaline additives and having a pH value above. of 11, preferably at least 13, and more preferably above 13.7.
Suitable examples of nonionic surfactants according to formula II are alkylene oxide adducts obtained by the alkoxylation of an alcohol or an amide. The group R in formula II can be branched or linear, saturated or unsaturated, aromatic or aliphatic. Examples of suitable hydrocarbon groups R 'are 2-ethylhexyl, octyl, decyl, cocoalkyl, lauryl, oleyl, rapeseed alkyl and bait alkyl. Particularly suitable hydrocarbon groups R 'are those obtained from oxoalcohols, Guerbet alcohols, methyl substituted alcohols, with 2 to 4 groups having the formula -CH (CH3) - included in the alkyl chain, and linear alcohols. Other suitable R groups are the aliphatic amido groups R''CONH-, where R "CO is preferably derived from aliphatic acids such as 2-ethylhexanoic acid, octanoic acid, decanoic acid, lauric acid, coconut fatty acid, oleic acid, fatty acid rapeseed oil and fatty acid bait. The alkali hydroxide in the composition is preferably sodium or potassium hydroxide. The alkaline complexing agent can be inorganic as well as organic. Typical examples of inorganic complex forming agents used in the alkaline composition are alkali salts of silicates and phosphates, such as sodium tripolyphosphate, sodium orthophosphate, sodium pyrophosphate, sodium phosphate and the corresponding potassium salts. Typical examples of organic complexing agents are alkaline aminopolyphosphonates, organic phosphates, polycarboxylates, such as citrates; aminocarboxylates, such as sodium trilotriacetate (Na3NTA), sodium ethylenediaminetetraacetate, sodium diethylenetriaminepentaacetate, sodium 1,3-propylenediaminetetraacetate, and sodium hydroxyethylethylenediaminetriacetate. The wetting of the composition is attributable to the nonionic surfactant present. Hexyl glycoside is not a wetting agent by itself, but by acting as a hydrotrope for the surfactant, it improves the wetting ability of the composition, since the otherwise insoluble surfactant is now dissolved and can exert its ability to wetting Concentrates with unexpectedly high amounts of surfactants can be dissolved in a highly alkaline aqueous phase, and the amount of hydrotrope required to obtain a stable, clear concentrate or composition is lower than in the prior art. This is very surprising, since in formulations with other short chain alkyl glycosides, it is not possible to include such large amounts of nonionic, surface active alkylene oxide adducts, as when the n-hexyl glucoside is present in the formulations For comparison, the formulations have also been made with shorter and longer alkyl glycosides, which are illustrated in Example 1. The composition of the present invention also shows controlled foam formation without the need to add foam depressants. , like those used in the prior art. The products in the composition all have good environmental properties. These are easily biodegradable and have low toxicity. The composition has an excellent wetting and cleaning ability and can be advantageously used for the alkaline cleaning of hard surfaces, for example, cleaning of vehicles, in a mercerization process and for a process of cleaning, desizing or scouring of fibers and fabrics performed at a pH above 11.
When used for cleaning hard surfaces, the composition is usually diluted with water before use, while in a mercerization process, the composition can be used as such. For cleaning, desizing and scouring of fibers and fabrics the composition should be either used as such or diluted. When woven fabrics are produced, the warp yarns are subject to extreme stresses and must therefore be provided with a protective coating - the squeezing agent - which adheres to the fiber, forming an elastic, abrasion resistant film. The two main groups of preparation agents are macromolecular natural products and their derivatives, for example starches and carboxymethylcellulose, and synthetic polymers, for example polyvinyl compounds. The dressing agent must be completely removed when the garment has been woven, as it usually has a damaging effect on the subsequent finishing processes. The sizing process can be enzymatic or oxidative, and is usually carried out to completion in the subsequent alkaline blanching and scouring stages, where the starch degradation products initially insoluble in water, and the residual binders are partially broken from hydrolitically and partially oxidatively, and eliminated. During the scouring, the intra- and intermolecular hydrogen bonds of the cellulose are broken, and the polar hydroxyl groups of the polysaccharide are solvated. The transport of the impurities from the internal part to the outer part of the fiber occurs then. In the alkaline environment the hydrolytic decomposition of the different plant parts and fats takes place and the waxes are also hydrolyzed. The alkali concentration used is approximately 4 to 6% when NaOH is used. In the scouring process there is a need for auxiliaries, to effect perfect wetting, emulsification and dispersion of insoluble impurities in water, formation of complexes of heavy metal ions and prevention of damage to the fiber by oxygen atmospheric. Here, alkali-stable wetting agents and detergents are an important group of additives. It is also very important that an adequate amount of wetting agent / detergent be soluble in the aqueous alkaline solution, which frequently requires the addition of a hydrotrope. The same applies to an even greater degree for the mercerization process, which is mainly carried out in order to improve the dyeing capacity of cotton. The process involves treating cotton under tension with approximately 20 to 26% caustic soda solution at 15 to 25 ° C for 25 to 40 seconds. This treatment destroys the spiral shape of cellulose, which improves the accessibility of water, and consequently, of water-based dyes. In addition to good wetting ability and alkaline stability, it is also important that the additives do not cause foaming, as this could impede the rapid wetting required in the mercerization baths. The present invention is further illustrated by the following examples.
Example 1
This example illustrates the amount of different hydrotropes of alkyl glucoside R0 (G) n, which is necessary to obtain clear solutions of 5% nonionic surfactant in solutions containing 10, 20, 30 and 40% NaOH. The nonionic surfactant used was an alcohol of 9 to 11 carbon atoms with a linearity above 80% which had been ethoxylated with 4 moles of ethylene oxide per mole of alcohol in the presence of a narrow-field catalyst. The glycosides tested are laboratory samples, except for the butyl glucoside which is a commercial sample of SEPPIC. The degree of polymerization falls between 1.4 and 1.6 with somewhat higher amounts of glucose for the longer alkyl chains.
Process :
% non-ionic surfactant was added to aqueous solutions with different amounts of sodium hydroxide. The hydrotropes tested were added dropwise at room temperature to those aqueous mixtures of nonionic and sodium hydroxide in an amount that was just sufficient to obtain a clear solution.
no clear solution was obtained, a glycoside based on an alcohol substituted with methyl, containing groups having the formula -CH (CH 3) - included in the alkyl chain.
From the results it is evident that the solubilization effect of the hexyl glucoside is superior to the solubilization effects of the alkyl glucosides used for the comparison.
Example 2
To compare the efficiency of n-hexyl glucoside to other types of hydrotropes, the same procedure as described in Example 1 was followed.
no clear solution was obtained
The tests show an unexpectedly good solubilization ability of n-hexyl glucoside, especially at high contents of alkaline material.
Example 3
The surface tension was measured according to du Nouy (DIN 53914). The first three solutions contained 5% of the same nonionic that was used in Examples 1 and 2, and the different amounts of the hydrotropes were the same as in Example 2. For the solutions containing only n-hexyl glucoside the amounts were (5 + x)%, where x represents the amounts used in Examples 1 and 2.
no clear solution was obtained, and the surface tension was not measured for these formulations.
Example 4
The modified Drave test was used to measure the wetting ability of highly alkaline compositions containing n-hexyl glucoside and non-ionic surfactants, in comparison to n-hexyl glucoside alone. In the modified Drave test, the immersion time in seconds is measured for a specified cotton yarn in approximately 0.1% surfactant solution. In this example, the concentrations for the hexyl glycoside and the non-ionic surfactant specified in the following table were used.
The decyl glucoside is used for a comparison, since it represents an example of a non-ionic surfactant which is soluble in aqueous alkaline solution in the absence of any hydrotrope. As can be seen from the table, n-hexyl glucoside has no ability to wet itself.
Example 5
The contact angle was measured with surfactant solutions, at concentrations specified in the following table, against a hydrophobic polymeric material (Parafilm). The angle is measured with a goniometer 1 minute after the application of the fluid. The decyl glucoside is used for a comparison.
Example 6
The foam is measured as mm of foam produced in a 500 ml measuring cylinder with internal diameter of 49 mm from a solution of 200 ml of surfactant when the cylinder is turned 40 times in one minute. The test is performed at room temperature and the height of the foam is recorded directly and after 1 and 5 minutes.
The decyl glucoside is used for a comparison.
Example 7
The following two formulations were prepared to evaluate the cleaning efficiency of a formulation using n-hexyl glucoside as a hydrotrope, compared to a formulation using sodium eumeno sulfonate as a hydrotrope.
11 This amount was necessary to obtain a clear solution.
The cleaning efficiency of the formulations in the above table was evaluated using the following cleaning test: Plates painted white were daubed with a mixture of oil-soot obtained from diesel engines. 25 ml of the test solutions are emptied onto the top of the plates smeared with oil and left there for one minute. The plates are then rinsed with a rich flow of water. All solutions and water are maintained at a temperature of approximately 15-20 ° C. Both test solutions were placed on the same plate. The reflectance of the plates was measured with a Minolta Chroma Meter CR-200 reflectometer before and after cleaning. The test was carried out with the concentrates and with the solutions diluted 1: 3 with water. Washed dirt was calculated by the computer program built into the meter, whereby for the formulation I according to the invention approximately 85% of washed dirt was obtained and for the reference formulation II about 44% washed dirt was obtained. For the diluted 1: 3 solutions, the corresponding amounts were 68 and 21% respectively. It was also found that, when n-hexyl glycoside is used as a hydrotrope, the hydrophobic powder which is emulsified in the cleaning process can be easily separated from the waste water after dilution with water. This is an important advantage, since there is a growing environmental demand for the low oil content in the wastewater.
Example 8
The following table shows some examples of how much n-hexyl glucoside is needed to obtain a clear solution in water with different types and amounts of non-ionic surfactants, with different amounts of Na3NTA added.
Claims (12)
1. The use of a hexyl glycoside having the formula C6H13OGn (I), wherein G is a monosaccharide residue and n is from 1 to 5, in a highly alkaline composition having a pH value above 11, containing an adduct of nonionic alkylene oxide, surface active, which is not soluble in the highly alkaline composition, and contains a hydrocarbon group or an acyl group of 8 to 24 carbon atoms, and at least one primary hydroxyl group in the alkoxylated part of the molecule, like a hydrotrope.
2. The use according to claim 1, wherein the adduct has the formula R (AO) x (C2H40) and H (II), where R is an alkoxy group R 'O- having 8 to 24 carbon atoms or a group R '' CONR '' '- where R "is a hydrocarbon group having 7 to 23 carbon atoms, R' '' is hydrogen or the group - (AO) x (C2H40) and H, AO is an alkyleneoxy group with 2 to 4 carbon atoms, x is a number from 0 to 5 and y is a number from 10.
3. The use according to claim 1 or 2, wherein the alkaline composition has a pH value above 134.
The use according to claims 1, 2 or 3, wherein the glycoside is an n-hexyl glycoside.
5. An aqueous alkaline composition having a pH value above 11, characterized in that it contains: a) 3 to 50% by weight of alkali metal hydroxide and / or alkaline complexing agents; b) 0.05 to 30% by weight of an adduct of nonionic alkylene oxide, surface active having a hydrocarbon group or an acyl group of 8 to 24 carbon atoms and having at least one primary hydroxyl group in the alkoxylated part of the molecule; c) 0.04 to 30% by weight of a hexyl glycoside; and d) 20 to 97% by weight of water.
6. A composition according to claim 5, characterized in that the nonionic surfactant is an alkoxylate having the formula R (A0) x (C2H4O) and H (II), wherein R is an alkoxy group R '0- having 8 a 24 carbon atoms or a group R "-CONR" '- where R "is a hydrocarbon group having 7 to 23 carbon atoms, R' '' is hydrogen or the group - (AO) x (C2H40) and H, AO is an alkyleneoxy group with 2 to 4 carbon atoms, x is a number from 0 to 5 and e is a number from 1 to 10.
7. A composition according to claims 1-6, wherein the weight ratio between c) and b) is from 1:10 to 4: 1.
8. A composition according to claims 5-7 having a pH value above 13.
9. A composition according to claims 5-8 wherein the hexyl glycoside is n-hexyl glycoside.
10. The use of the alkaline composition according to claims 5-9, in a mercerization process.
11. The use of the alkaline composition according to claims 5-9 in a hard surface cleaning process.
12. The use of the alkaline composition according to claims 5-9 in a process of cleaning, deburring or scouring fibers and fabrics.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE9703946-5 | 1997-10-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA00003481A true MXPA00003481A (en) | 2001-05-07 |
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