US3915878A - Free flowing nonionic surfactants - Google Patents
Free flowing nonionic surfactants Download PDFInfo
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- US3915878A US3915878A US335873A US33587373A US3915878A US 3915878 A US3915878 A US 3915878A US 335873 A US335873 A US 335873A US 33587373 A US33587373 A US 33587373A US 3915878 A US3915878 A US 3915878A
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- United States
- Prior art keywords
- nonionic
- free flowing
- weight
- detergent
- silica
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- Expired - Lifetime
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- 239000002736 nonionic surfactant Substances 0.000 title abstract description 46
- 239000003599 detergent Substances 0.000 claims abstract description 53
- 238000000034 method Methods 0.000 claims abstract description 34
- 239000007788 liquid Substances 0.000 claims abstract description 33
- 239000007921 spray Substances 0.000 claims abstract description 14
- 238000002156 mixing Methods 0.000 claims abstract description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 72
- 239000000843 powder Substances 0.000 claims description 31
- 239000000377 silicon dioxide Substances 0.000 claims description 27
- 239000004094 surface-active agent Substances 0.000 claims description 12
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 9
- 230000001698 pyrogenic effect Effects 0.000 claims description 7
- 239000002245 particle Substances 0.000 claims description 6
- 238000001694 spray drying Methods 0.000 claims description 6
- 239000002002 slurry Substances 0.000 claims description 5
- 239000004965 Silica aerogel Substances 0.000 claims description 4
- 239000000499 gel Substances 0.000 claims description 3
- 150000001721 carbon Chemical group 0.000 claims description 2
- 230000006872 improvement Effects 0.000 claims description 2
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 48
- 238000009472 formulation Methods 0.000 abstract description 27
- 239000000463 material Substances 0.000 abstract description 9
- 239000012876 carrier material Substances 0.000 abstract description 5
- UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 abstract description 2
- 150000001875 compounds Chemical class 0.000 abstract description 2
- 238000011068 loading method Methods 0.000 description 20
- 229910019142 PO4 Inorganic materials 0.000 description 13
- 239000000969 carrier Substances 0.000 description 13
- 235000021317 phosphate Nutrition 0.000 description 13
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 12
- 239000010452 phosphate Substances 0.000 description 12
- 235000012239 silicon dioxide Nutrition 0.000 description 11
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 10
- 239000011236 particulate material Substances 0.000 description 9
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
- 159000000000 sodium salts Chemical class 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 7
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical class OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 6
- 229940023144 sodium glycolate Drugs 0.000 description 6
- JEJAMASKDTUEBZ-UHFFFAOYSA-N tris(1,1,3-tribromo-2,2-dimethylpropyl) phosphate Chemical compound BrCC(C)(C)C(Br)(Br)OP(=O)(OC(Br)(Br)C(C)(C)CBr)OC(Br)(Br)C(C)(C)CBr JEJAMASKDTUEBZ-UHFFFAOYSA-N 0.000 description 6
- 239000004471 Glycine Substances 0.000 description 5
- 239000001509 sodium citrate Substances 0.000 description 5
- 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 5
- 238000007711 solidification Methods 0.000 description 5
- 230000008023 solidification Effects 0.000 description 5
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 4
- -1 aromatic sulfonates Chemical class 0.000 description 4
- 239000000440 bentonite Substances 0.000 description 4
- 229910000278 bentonite Inorganic materials 0.000 description 4
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 4
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 239000007844 bleaching agent Substances 0.000 description 3
- 238000012851 eutrophication Methods 0.000 description 3
- 239000013020 final formulation Substances 0.000 description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- XSVSPKKXQGNHMD-UHFFFAOYSA-N 5-bromo-3-methyl-1,2-thiazole Chemical compound CC=1C=C(Br)SN=1 XSVSPKKXQGNHMD-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000001449 anionic compounds Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 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 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-L L-tartrate(2-) Chemical compound [O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O FEWJPZIEWOKRBE-JCYAYHJZSA-L 0.000 description 1
- 102000016462 Phosphate Transport Proteins Human genes 0.000 description 1
- 108091007643 Phosphate carriers Proteins 0.000 description 1
- RLUDBKMUNGUSSY-UHFFFAOYSA-N [Si](=O)=O.[Na] Chemical compound [Si](=O)=O.[Na] RLUDBKMUNGUSSY-UHFFFAOYSA-N 0.000 description 1
- WDJHALXBUFZDSR-UHFFFAOYSA-M acetoacetate Chemical compound CC(=O)CC([O-])=O WDJHALXBUFZDSR-UHFFFAOYSA-M 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 229960004275 glycolic acid Drugs 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 239000008239 natural water Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- BITYAPCSNKJESK-UHFFFAOYSA-N potassiosodium Chemical compound [Na].[K] BITYAPCSNKJESK-UHFFFAOYSA-N 0.000 description 1
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 1
- 229940074439 potassium sodium tartrate Drugs 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- 239000011856 silicon-based particle Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- DZCAZXAJPZCSCU-UHFFFAOYSA-K sodium nitrilotriacetate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CC([O-])=O DZCAZXAJPZCSCU-UHFFFAOYSA-K 0.000 description 1
- 239000012418 sodium perborate tetrahydrate Substances 0.000 description 1
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- IBDSNZLUHYKHQP-UHFFFAOYSA-N sodium;3-oxidodioxaborirane;tetrahydrate Chemical compound O.O.O.O.[Na+].[O-]B1OO1 IBDSNZLUHYKHQP-UHFFFAOYSA-N 0.000 description 1
- 229960002920 sorbitol Drugs 0.000 description 1
- 239000000271 synthetic detergent Substances 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D11/00—Special methods for preparing compositions containing mixtures of detergents
- C11D11/0082—Special methods for preparing compositions containing mixtures of detergents one or more of the detergent ingredients being in a liquefied state, e.g. slurry, paste or melt, and the process resulting in solid detergent particles such as granules, powders or beads
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
Definitions
- ABSTRACT A method for converting liquid nonionic surfactants to dry free flowing form is disclosed.
- the new method includes the mixing of the liquid nonionic material with specific particulate carrier materials in amounts L varying from 30 to 85 percent.
- Suitable carrier materig als include compounds having functional properties in detergent formulations.
- the free flowing nonionic surfactant-carrier pre-mix is very suitable for postaddition to spray dried detergent formulations in order to increase their content of nonionic surfactant.
- the invention pertains to heavy duty particulated detergent formulations that include anionic, cationic, or nonionic surface active agents and detergent builders. More specifically the invention provides heavy duty detergents having a relatively high content of nonionic surface active agent.
- anionic compounds having detersive properties. Typical of these anionic compounds are the higher alkyl mononuclear aromatic sulfonates such as the higher alkyl benzene sulfonates. These synthetic detergents are very effective in removing dirt from textile fabrics when utilized in conjunction with phosphate builders which function to soften the water being used and to provide detersive action.
- phosphate builders which function to soften the water being used and to provide detersive action.
- considerable controversy exist today as to the efficacy of utilizing phosphate compounds in detergent formulations due to their alleged causation of the eutrophication process in lakes, rivers and streams. Although the eutrophication process, wherein an excessive growth of plant life is promulgated in natural water bodies, is not completely understood, it is alleged that the phosphate compounds present in detergent containing waste water are a prime factor in promoting this phenomenon.
- nonionic surfactants are not as effective as anionic surfactants in the presence of large amounts of phosphate builders, it has been discovered that when the phosphate content of a detergent formulation is substantially reduced, the nonionic surfactants appear to provide detergency properties that are superior to anionics in the same reduced phosphate content formulation. Apparently the detersive effectiveness of nonionic surfactants is affected much less by water hardness than that of the commonly used anionic surfactants. In the event that phosphate builders are totally or partially removed from detergents, the incorporation of greater and greater amounts of nonionic surfactants into detergent formulations will become very desirable.
- nonionic surfactants are added to detergent formulations, primarily to reduce the amount of foam generated during the washing cycle.
- the most commonly used nonionic surfactants are long carbon chain alcohols ethoxylated with ethylene oxide.
- the nonionic ethoxamer used has a 12 to 18 carbon atom alkyl chain and an average of about to 19 ethylene oxide units.
- the primary objective of the present invention is to provide a method for converting liquid nonionic surfactants to dry free flowing particulate form so that they may be post added to spray dried detergent formulations and thereby significantly increase the nonionic surfactant content of the final detergent product.
- the maximization of the nonionic surfactant content of the i post addable free flowing powder and the selection of particularly suitable carriers for the nonionic materials are important further objectives of the invention.
- the present invention provides a method for obtaining free flowing particulate materials having a nonionic jv surfactant content of up to about 85% by weight, and
- the new materials are i very suitable for post addition to spray dried detergent powders in order to substantiallyraise the nonionic surfactant content of the finished detergent product.
- the inven- I tion provides a specific carrier materials for nonionic surfactants that are capable of high nonionic loadings; some of which also contribute functional characteristics to the detergent formulation.
- particulate silica substances in general, and microsized silicon dioxide particles in particular are capable of carrying a high loading (about 85% by weight) of nonionic surfactant without losing their free flowing characteristics.
- a method for preparing free flowing particulate premix including a high loading, preferably from 62 to about; 85% by weight, most preferably about 65 to by weight, of liquid nonionic surface active agent and microsized silica particles is provided.
- the premix is particulary suitable for addition to a detergent powder formed by spray drying a detergent slurry according to well known procedures, to produce a final formulation 3 having a desirably high content of nonionic surface active agent.
- the premix is advantageously produced by mixing the nonionic with a sufficient amount of microsized silica particles to result in a free flowing powder.
- the amount of microsized silica particles used to solid-i ify the nonionic into free flowing form is above 5% by. weight of the mixture, usually between more than about 5% by weight up to about 38%, preferably about 25%, by weight.
- microsized silicon particles are used as an anti caking agent in some detergent formulations, its use as a liquid nonionic carrier provides anti-caking properties as well as higher nonionic content to the detergent formulation it is ultimately combined with. Further the aforementioned silica substances, when added to a mixf ture of nonionic surfactant and other carriers, in accorf dance with the invention, substantially increases thq' maximum nonionic loading of the resulting post addable, free flowing mix. f
- liquid nonionic surfactants are substances having building properties in the detergent formulations. in view of the desirability of reducing, and if possible eliminating, the phosphate con? tent of detergent formulations, the use of other builder: in conjunction with a higher concentration of nonioni surfactant is advantageous.
- certain non-phosphate detergent builder! are suitable carriers for liquid nonionic surfactants Representative of these builder-carrier substances are the sodium salts of nitrilotriacetic acid (NTA). sodium carbonate and sodium citrate. Loadings of up to about 50% by weight of nonionic surfactant have been obtained with these builder-carriers either individually or in combination with each other in multi-component systems.
- the nonionic loading of these builder-carriers can be increased to over about 60 weight percent by adding a small amount, typically about 5 percent by weight, of a silica substance, preferably microsized silicon dioxide particles to the blend.
- a silica substance preferably microsized silicon dioxide particles
- pyrogenic microsized silicon dioxide particles are preferred in the practice of the invention other microsized silicon dioxide particles such as silica gel and diatomaceous silica have given satisfactory results.
- peroxygen bleaching agents have been found to be suitable carriers for nonionic surfactants while still retaining their free flowing properties.
- Peroxygen bleaching agents are advantageous carriers for liquid nonionic surfactants when it is also desirable to include a bleaching component in the final formulation. This is particularly so when only one post addition operation can be performed since both post additives can be added simultaneously in accordance with this aspect of the invention.
- nonionic surfactant utilized was an ethoxylated long chain alcohol having a chain of 12 to 16 carbon atoms and to l2 ethylene oxide units.
- a suitable ethoxamer is available from the Shell Chemical Company under the trademark NEODOL 45-11.
- NEODOL 45-11 is a 14 to 15 carbon chain ethoxylated fatty alcohol having an average of l l ethylene oxide units.
- microzied silica particulate material used is available under the trademark CabO-Sil, grade EH-S from the Cabot Company.
- Cab- 'O-Sil is a sub-microscopic particle size silica prepared by vapor phase hydrolysis of silicon tetrachloride at l 100C. All experimental runs were made at room temperature and atmospheric pressure.
- Other suitable microsized silica materials are available under the following trademarks: silica aerogel available from the Monsanto Chemical Company, Quso which is a precipitated silica which has a surface area of about 325 square meters per square meters per gram and Syloid 244, which is a low density gel available from W. R. Grace Company.
- Example 1 Fifty grams of molten nonionic surfactant was heated to slightly above room temperature until clear appearance and then sprayed onto 10 grams of colloidal pyrogenie silicon dioxide. The resulting mixture was a free flowing powder having a nonionic loading of 83.3% by weight. The following techniques were used.
- the liquid nonionic was sprayed onto a laboratory dish containing the silicon dioxide carrier and mixed with a spatula to produce a free flowing powder.
- An example of the latter procedure is to first prepare a free flowing powder consisting of 250.0 grams of a liquid nonionic surfactant and 50.0 grams of silicon dioxide carrier (83.3 weight percent nonionic). To this blend 100.0 grams of sodium salts of (NTA) and 100.0 grams of sodium citrate when added and blended to produce a finished deterent formulation having the following approximate composition:
- Example 2 The liquid nonionic surfactant was slowly added to a laboratory mortar containing any one or a combination of the following inorganic particulate materials: sodium carbonate, clays (such as bentonite and zeolite), diatomaccous earth (Celite Filteraid available from Johns- Manville Company) or aluminum oxide. Upon blending the liquid nonionic and the inorganic particulate material with a pestle, partial solidification of the mixture occurs. Upon setting at room temperature for about one hour a free flowing powder is obtained.
- inorganic particulate materials sodium carbonate, clays (such as bentonite and zeolite), diatomaccous earth (Celite Filteraid available from Johns- Manville Company) or aluminum oxide.
- liquid nonionic loadings as high as by weight can be obtained without impairing the flowability of the resulting solid particulate material.
- Example 3 From 50 to 80 weight percent of the liquid nonionic surfactant was blended with a mixture of 15 to 45 weight percent of an organic nitrogenous compound chosen from the group consisting of melamine, glycine and iminodiacetic acid and from to 50 percent by weight of any one or a mixture of the inorganic carriers of Example 2. Upon mixing, partial solidification occurs. The addition of at least percent by weight of colloidal pyrogenic silicon dioxide and subsequent thorough blending results in solidification of the mixture. The solidified mixture can be broken up into a free flowing, non-caking powder. The following free flowing powder compositions have been obtained by the foregoing method:
- Example 5 The procedures and compositions of Example 4 were followed except that a non-nitrogenous organic material chosen from the group consisting of sodium glycolate, glycolic acid, sorbitol, and potassium sodium tartrate, was substituted for the nitrogen containing organic compounds.
- a non-nitrogenous organic material chosen from the group consisting of sodium glycolate, glycolic acid, sorbitol, and potassium sodium tartrate.
- nonionic 60 weight percent zeolite l3 sodium glycolate l0 (3) nonionic 66.6 weight percent potassium sodium l6.8 tartrate SiO, 16.6
- Example 6 The liquid nonionic surfactant was mixed with trisodium nitrilotriacetate and sodium citrate-2H,O. Partial solidification occurred on mixing. Pyrogenic silicon dioxide was then added and thoroughly mixed with the partially solidified mass. Full solidification of the mixture occurred. The resulting solid was then broken up into a free flowing, non-caking powder.
- the following composition has been obtained by the foregoing method:
- nonionic surfactant 56.6 weight percent sodium salt of NTA l3.0 sodium citrate 13.0 SiO, 17.4
- the resulting free flowing powder is very suitable for post addition to a spray dried detergent powder. Similar free flowing powder can be obtained without the addition of SiO, by reducing the nonionic content to about 30 percent by weight.
- Example 7 nonionic surfactant 60.0 weight percent sodium salt of NTA l5.0 sodium carbonate l5.0 SiO, 10.0
- the resulting free flowing powder is very suitable for post addition to a spray dried detergent powder.
- Example 8 35 weight percent of liquid nonionic surfactant is blended together with 65 weight percent sodium perborate monohydrate. The resulting mixture is a free flowing powder suitable for post addition to spray dried detergent formulations.
- Example 9 A free flowing particulate material having a nonionic 7 surface active agent content of 68% by weight can be prepared by the following procedure: 68 grams of Neov dol 45-11 was heated to slightly above room temperature until molten and clear in appearance. The molen i nonionic surface active agent was slowly added to 32 grams of Cab-O-Sil EI-l-S, a micro-sized silica powder, and the combination was mixed by mechanical stirring for about 5 minutes. The resulting product is a free flowing powder.
- Example l The procedure of Example 9 can be repeated using 62 grams of Neodol 45-1l and 38 grams of Cab-O-Sil EH-S to produce a free flowing powder having a nonionic loading of 62% by weight.
- Example II The procedure of Example 9 is repeated using 75 grams of Neodol 45-1l and 25 grams of Cab-O-Sil EH- to produce a free flowing powder having a nonionic loading of 75% by weight.
- the free flowing products produced by Examples 9-ll are ideally suitable for post addition to a detergent powder made by spray drying a detergent slurry according to well known procedures in the detergent art.
- Final detergent formulations produced by combining spray dried detergents with the free flowing particulate pre-mixes of the invention can comprise from about 10 to about 50% of the post-added premix component to provide a wide range of nonionic content depending on the nonionic loading of the premix and the requirements of the particular application.
- Example I2 320 grams of a particulate silica material sold under the trademark Santocel, which is a silica aerogel, was
- Example 13 The procedure of Example 12 was repeated using a particulate silica material available under the trademark Quso. Quso is a precipitated silica having a surface area of 325 m'lgram and a 5% water content. The resulting product was a free flowing particulate material having a nonionic loading of 68% by weight.
- Example 14 The procedure of Example 12 was repeated using a particulate silica material available under the trademark Syloid 244.
- Syloid 244 is a low density silica gel.
- the resulting product is a free flowing particulate material having a nonionic loading of 68% by weight.
- Runs similar to Examples l-l4 can be made using liquid nonionic surfactants having a longer alkyl chain than Neodol 45-ll, i.e. 16-18 carbon atoms, and a higher ethylene oxide content, i.e. an average of 19 ethylene oxide units.
- a suitable liquid nonionic meeting these requirements is available from the Continental Oil Company under the trademark Alfonic 1618-78. It was found that, Alfonic l6l8-78 can be solidified with less effort, i.e. in less time, than Neodol 45-11 and to approximately the same loadings.
- Noncaking powders that can be heavily loaded with nonionic surfactants and still remain free flowing, noncaking powders were found to include pyrogenic silicon dioxide, which functions as an anti-caking agent in the final formulation, and various detergent builders such as NTA, sodium carbonate and sodium citrate.
- phosphate detergent builders have also been found to be very suitable carriers for liquid nonionic surfactants, their use is not preferred at this time because of the alleged contribution of phosphates to the eutrophication process in natural bodies of water.
- all or part of the phosphate builder can be added to the formulation subsequent to spray drying as a carrier for nonionic surfactants.
- phosphate builders such as the sodium tripolyphosphate can be loaded with up to about 30 percent by weight liquid nonionic surfactant while still retaining free flowing properties.
- the nonionic loading on phosphate carriers can be increased to about 50 percent by weight by adding about 5 percent by weight of a microsized silica substance to the nonionic-carrier mixture before final setting.
- the invention represents a significant step towards the substantial reduction of phosphate builders from detergent formulations without a significant decrease in cleaning efficacy.
- the method of preparing a heavy duty detergent which includes the step of spray drying a detergent slurry to form a dry, free flowing powder, the improvement comprising adding to said spray dried powder a free flowing premix consisting of from 62 to 85 percent by weight of a liquid nonionic surface active agent chosen from the group consisting of ethoxylated alcohols having a 12 to 18 carbon atom chain and an average of from 10 to 19 ethylene oxide units and at least 5% by weight of microsized silica particles, said premix being prepared by mixing said liquid nonionic with a sufficient quantity of silica particles to fully solidify said liquid nonionic.
- a liquid nonionic surface active agent chosen from the group consisting of ethoxylated alcohols having a 12 to 18 carbon atom chain and an average of from 10 to 19 ethylene oxide units and at least 5% by weight of microsized silica particles
- micro-sized silica particles are chosen from the group consisting of silica gels, silica aerogels, precipitated silicas and pyrogenic silicas.
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Abstract
A method for converting liquid nonionic surfactants to dry free flowing form is disclosed. The new method includes the mixing of the liquid nonionic material with specific particulate carrier materials in amounts varying from 30 to 85 percent. Suitable carrier materials include compounds having functional properties in detergent formulations. The free flowing nonionic surfactantcarrier pre-mix is very suitable for post-addition to spray dried detergent formulations in order to increase their content of nonionic surfactant.
Description
AU 16S United States Patent [1 1 Yurko et al.
[ 1 FREE FLOWING NONIONIC SURFACTANTS [75] Inventors: Joseph A. Yurko, Bayonne;
Pallassana Ramachandran, Robinsville; Bao-Ding Cheng, Highland Park; Robert E. Dickson, Bellemead, all of NJ.
[73] Assignee: Colgate-Palmolive Company, New
York, N.Y.
[ 1 Notice: The portion of the term of this patent subsequent to Oct. 30, 1990, has been disclaimed.
[22] Filed: Feb. 26, 1973 [21] Appl. No.: 335,873
Related US. Application Data [63] Continuation-impart of Ser. No. 114,073, Feb. 9,
1971, Pat. No. 3,769,222.
[52] US. Cl. 252/89; 252/99; 252/D1G. l
[51] Int. Cl. CllD 1/72; Cl 1D 11/00 [58] Field of Search 252/89, 99, 135, 546, DIG. l
{56] References Cited UNITED STATES PATENTS 3,337,463 8/1967 Schmolka 252/89 3,562,171 2/1971 Guida 252/186 2/ l 972 Muller 252/404 *Oct. 28, 1975 3,666,670 5/1972 Gilbert et a1 252/160 3,769,222 10/1973 Yurko et al...... 252/89 FOREIGN PATENTS OR APPLICATIONS 918,499 2/1963 United Kingdom 252/89 709,515 5/1954 United Kingdom 252/89 3 807,640 1/1959 United Kingdom 252/89 511,415 3/1955 Canada 252/89 OTHER PUBLICATIONS Schue, Detergents and Specialties," 6, No. 3, pp. CT 18, 21, 22 & 24 (March 1969).
[57] ABSTRACT A method for converting liquid nonionic surfactants to dry free flowing form is disclosed. The new method includes the mixing of the liquid nonionic material with specific particulate carrier materials in amounts L varying from 30 to 85 percent. Suitable carrier materig als include compounds having functional properties in detergent formulations. The free flowing nonionic surfactant-carrier pre-mix is very suitable for postaddition to spray dried detergent formulations in order to increase their content of nonionic surfactant.
4 Claims, No Drawings FREE FLOWING NONIONIC SURFACTANTS Related Applications This application is a continuation-in-part of copending application Ser. No. 1 14,073 filed Feb. 9, 197] and entitled Free Flowing Nonionic Surfactants, and now US. Pat. No. 3,769,222 issued Oct. 30, 1973.
The invention pertains to heavy duty particulated detergent formulations that include anionic, cationic, or nonionic surface active agents and detergent builders. More specifically the invention provides heavy duty detergents having a relatively high content of nonionic surface active agent.
The most commonly used surface active agents in heavy duty detergent formulations are anionic compounds having detersive properties. Typical of these anionic compounds are the higher alkyl mononuclear aromatic sulfonates such as the higher alkyl benzene sulfonates. These synthetic detergents are very effective in removing dirt from textile fabrics when utilized in conjunction with phosphate builders which function to soften the water being used and to provide detersive action. However, considerable controversy exist today as to the efficacy of utilizing phosphate compounds in detergent formulations due to their alleged causation of the eutrophication process in lakes, rivers and streams. Although the eutrophication process, wherein an excessive growth of plant life is promulgated in natural water bodies, is not completely understood, it is alleged that the phosphate compounds present in detergent containing waste water are a prime factor in promoting this phenomenon.
Although nonionic surfactants are not as effective as anionic surfactants in the presence of large amounts of phosphate builders, it has been discovered that when the phosphate content of a detergent formulation is substantially reduced, the nonionic surfactants appear to provide detergency properties that are superior to anionics in the same reduced phosphate content formulation. Apparently the detersive effectiveness of nonionic surfactants is affected much less by water hardness than that of the commonly used anionic surfactants. In the event that phosphate builders are totally or partially removed from detergents, the incorporation of greater and greater amounts of nonionic surfactants into detergent formulations will become very desirable.
At present, small amounts of nonionic surfactants are added to detergent formulations, primarily to reduce the amount of foam generated during the washing cycle. The most commonly used nonionic surfactants are long carbon chain alcohols ethoxylated with ethylene oxide. Typically, the nonionic ethoxamer used has a 12 to 18 carbon atom alkyl chain and an average of about to 19 ethylene oxide units. The range of ethylene oxide content that provides the greatest detergency in slurry before spray drying, a significant air pollution problem is encountered. This problem, known in the industry as pluming", is manifested as a dense black smoke being discharged from the spray tower.
The primary objective of the present invention is to provide a method for converting liquid nonionic surfactants to dry free flowing particulate form so that they may be post added to spray dried detergent formulations and thereby significantly increase the nonionic surfactant content of the final detergent product. The maximization of the nonionic surfactant content of the i post addable free flowing powder and the selection of particularly suitable carriers for the nonionic materials are important further objectives of the invention.
The present invention provides a method for obtaining free flowing particulate materials having a nonionic jv surfactant content of up to about 85% by weight, and
preferably above 30% by weight, and most preferably, between 62 and 85% by weight. The new materials are i very suitable for post addition to spray dried detergent powders in order to substantiallyraise the nonionic surfactant content of the finished detergent product. ln 1.- order to achieve an optimum post additive mixture for spray dried detergent fomulations, it is desirable to maximize the loading of nonionic surfactant on the chosen carrier and also to choose carriers that contribute to the efficacy of the detergent product. The inven- I tion provides a specific carrier materials for nonionic surfactants that are capable of high nonionic loadings; some of which also contribute functional characteristics to the detergent formulation.
In accordance with the invention, it has been found that particulate silica substances in general, and microsized silicon dioxide particles in particular, are capable of carrying a high loading (about 85% by weight) of nonionic surfactant without losing their free flowing characteristics. Pursuant to this aspect of the invention, a method for preparing free flowing particulate premix, including a high loading, preferably from 62 to about; 85% by weight, most preferably about 65 to by weight, of liquid nonionic surface active agent and microsized silica particles is provided. The premix is particulary suitable for addition to a detergent powder formed by spray drying a detergent slurry according to well known procedures, to produce a final formulation 3 having a desirably high content of nonionic surface active agent. The premix is advantageously produced by mixing the nonionic with a sufficient amount of microsized silica particles to result in a free flowing powder.; The amount of microsized silica particles used to solid-i ify the nonionic into free flowing form is above 5% by. weight of the mixture, usually between more than about 5% by weight up to about 38%, preferably about 25%, by weight.
Since microsized silicon particles are used as an anti caking agent in some detergent formulations, its use as a liquid nonionic carrier provides anti-caking properties as well as higher nonionic content to the detergent formulation it is ultimately combined with. Further the aforementioned silica substances, when added to a mixf ture of nonionic surfactant and other carriers, in accorf dance with the invention, substantially increases thq' maximum nonionic loading of the resulting post addable, free flowing mix. f
Other desirable carriers for liquid nonionic surfactants are substances having building properties in the detergent formulations. in view of the desirability of reducing, and if possible eliminating, the phosphate con? tent of detergent formulations, the use of other builder: in conjunction with a higher concentration of nonioni surfactant is advantageous. In this regard it has been found that certain non-phosphate detergent builder! are suitable carriers for liquid nonionic surfactants Representative of these builder-carrier substances are the sodium salts of nitrilotriacetic acid (NTA). sodium carbonate and sodium citrate. Loadings of up to about 50% by weight of nonionic surfactant have been obtained with these builder-carriers either individually or in combination with each other in multi-component systems. The nonionic loading of these builder-carriers can be increased to over about 60 weight percent by adding a small amount, typically about 5 percent by weight, of a silica substance, preferably microsized silicon dioxide particles to the blend. Although pyrogenic microsized silicon dioxide particles are preferred in the practice of the invention other microsized silicon dioxide particles such as silica gel and diatomaceous silica have given satisfactory results.
in further accordance with the invention, certain peroxygen bleaching agents have been found to be suitable carriers for nonionic surfactants while still retaining their free flowing properties. Peroxygen bleaching agents are advantageous carriers for liquid nonionic surfactants when it is also desirable to include a bleaching component in the final formulation. This is particularly so when only one post addition operation can be performed since both post additives can be added simultaneously in accordance with this aspect of the invention.
in the following examples maximum loadings of liquid nonionic surfactant were applied to various particulate carriers. The maximum loading was determined by adding increasing amounts of nonionic to a given amount of carrier until the resulting mixture could not be solidified into a free flowing powder. In examples 1-14 the nonionic surfactant utilized was an ethoxylated long chain alcohol having a chain of 12 to 16 carbon atoms and to l2 ethylene oxide units. A suitable ethoxamer is available from the Shell Chemical Company under the trademark NEODOL 45-11. NEODOL 45-11, according to its manufacturer, is a 14 to 15 carbon chain ethoxylated fatty alcohol having an average of l l ethylene oxide units. The microzied silica particulate material used is available under the trademark CabO-Sil, grade EH-S from the Cabot Company. Cab- 'O-Sil is a sub-microscopic particle size silica prepared by vapor phase hydrolysis of silicon tetrachloride at l 100C. All experimental runs were made at room temperature and atmospheric pressure. Other suitable microsized silica materials are available under the following trademarks: silica aerogel available from the Monsanto Chemical Company, Quso which is a precipitated silica which has a surface area of about 325 square meters per square meters per gram and Syloid 244, which is a low density gel available from W. R. Grace Company.
Example 1 Fifty grams of molten nonionic surfactant was heated to slightly above room temperature until clear appearance and then sprayed onto 10 grams of colloidal pyrogenie silicon dioxide. The resulting mixture was a free flowing powder having a nonionic loading of 83.3% by weight. The following techniques were used.
I. The liquid nonionic was sprayed onto a laboratory dish containing the silicon dioxide carrier and mixed with a spatula to produce a free flowing powder.
method can be post added to spray dried detergent powders or, detergent builders and other detergent in gredients can be added to the nonionic powder to produce a finished detergent formulation.
An example of the latter procedure is to first prepare a free flowing powder consisting of 250.0 grams of a liquid nonionic surfactant and 50.0 grams of silicon dioxide carrier (83.3 weight percent nonionic). To this blend 100.0 grams of sodium salts of (NTA) and 100.0 grams of sodium citrate when added and blended to produce a finished deterent formulation having the following approximate composition:
nonionic surfactant silicon dioxide sodium salt of NTA sodium citrate 50 weight percent 10 weight percent 20 weight percent 20 weight percent This later formula can be utilized as a detergent itself or as an additive to other detergent systems.
Example 2 The liquid nonionic surfactant was slowly added to a laboratory mortar containing any one or a combination of the following inorganic particulate materials: sodium carbonate, clays (such as bentonite and zeolite), diatomaccous earth (Celite Filteraid available from Johns- Manville Company) or aluminum oxide. Upon blending the liquid nonionic and the inorganic particulate material with a pestle, partial solidification of the mixture occurs. Upon setting at room temperature for about one hour a free flowing powder is obtained.
Using the foregoing method, liquid nonionic loadings as high as by weight can be obtained without impairing the flowability of the resulting solid particulate material.
Example 3 Example 4 From 50 to 80 weight percent of the liquid nonionic surfactant was blended with a mixture of 15 to 45 weight percent of an organic nitrogenous compound chosen from the group consisting of melamine, glycine and iminodiacetic acid and from to 50 percent by weight of any one or a mixture of the inorganic carriers of Example 2. Upon mixing, partial solidification occurs. The addition of at least percent by weight of colloidal pyrogenic silicon dioxide and subsequent thorough blending results in solidification of the mixture. The solidified mixture can be broken up into a free flowing, non-caking powder. The following free flowing powder compositions have been obtained by the foregoing method:
(I) nonionic 63.6 weight percent melamine 18.1 SiO, l8.3
(2) nonionic 70 weight percent sodium salt of glycine or imino- 20 diacetic acid SiO, l0
(3) nonionic 80 weight percent sodium salt of 3 glycine or iminodiacetic acid bentonite 7 SiO, l0
(4) nonionlc 80 weight percent sodium salt of glycine or iminodiacetic acid SiO l0 (5) nonionic 80 weight percent sodium salt of 3 glycine or iminodiacetic acid SiO, l5
Example 5 The procedures and compositions of Example 4 were followed except that a non-nitrogenous organic material chosen from the group consisting of sodium glycolate, glycolic acid, sorbitol, and potassium sodium tartrate, was substituted for the nitrogen containing organic compounds. The following free flowing powder formulations were obtained by the foregoing method:
( l nonionic 50 weight percent bentonite 30 sodium glycolate l0 SiO, l0
(2) nonionic 60 weight percent zeolite l3 sodium glycolate l0 (3) nonionic 66.6 weight percent potassium sodium l6.8 tartrate SiO, 16.6
(4) nonionic 50 weight percent sorbitol 24 SiO, 26
(5) nonionic 70 weight percent glycolic acid l0 SiO,
(6) nonionic 80 weight percent sodium glycolate 8 bentonite 2 SiO, l0
(7) nonionic 70 weight percent sodium glycolate 20 '0, l0
(8) nonionic 70 weight percent sodium glycolate l0 aluminum oxide l0 SiO,
Example 6 The liquid nonionic surfactant was mixed with trisodium nitrilotriacetate and sodium citrate-2H,O. Partial solidification occurred on mixing. Pyrogenic silicon dioxide was then added and thoroughly mixed with the partially solidified mass. Full solidification of the mixture occurred. The resulting solid was then broken up into a free flowing, non-caking powder. The following composition has been obtained by the foregoing method:
nonionic surfactant 56.6 weight percent sodium salt of NTA l3.0 sodium citrate 13.0 SiO, 17.4
The resulting free flowing powder is very suitable for post addition to a spray dried detergent powder. Similar free flowing powder can be obtained without the addition of SiO, by reducing the nonionic content to about 30 percent by weight.
Example 7 nonionic surfactant 60.0 weight percent sodium salt of NTA l5.0 sodium carbonate l5.0 SiO, 10.0
The resulting free flowing powder is very suitable for post addition to a spray dried detergent powder.
Example 8 35 weight percent of liquid nonionic surfactant is blended together with 65 weight percent sodium perborate monohydrate. The resulting mixture is a free flowing powder suitable for post addition to spray dried detergent formulations.
-- 1' "new:
Attempts to use sodium perborate tetrahydrate as a i carrier for the liquid nonionic yielded a tacky non-1 flowable powder with a nonionic liquid content of about 20 percent by weight.
Example 9 A free flowing particulate material having a nonionic 7 surface active agent content of 68% by weight can be prepared by the following procedure: 68 grams of Neov dol 45-11 was heated to slightly above room temperature until molten and clear in appearance. The molen i nonionic surface active agent was slowly added to 32 grams of Cab-O-Sil EI-l-S, a micro-sized silica powder, and the combination was mixed by mechanical stirring for about 5 minutes. The resulting product is a free flowing powder.
Example l The procedure of Example 9 can be repeated using 62 grams of Neodol 45-1l and 38 grams of Cab-O-Sil EH-S to produce a free flowing powder having a nonionic loading of 62% by weight.
Example II The procedure of Example 9 is repeated using 75 grams of Neodol 45-1l and 25 grams of Cab-O-Sil EH- to produce a free flowing powder having a nonionic loading of 75% by weight.
The free flowing products produced by Examples 9-ll are ideally suitable for post addition to a detergent powder made by spray drying a detergent slurry according to well known procedures in the detergent art. Final detergent formulations produced by combining spray dried detergents with the free flowing particulate pre-mixes of the invention can comprise from about 10 to about 50% of the post-added premix component to provide a wide range of nonionic content depending on the nonionic loading of the premix and the requirements of the particular application.
Example I2 320 grams of a particulate silica material sold under the trademark Santocel, which is a silica aerogel, was
' introduced into a Hobart mixer. The stirrer was turned on (low speed) and 680 grams ofa nonionic surface active agent (Neodol 45-11) in molten form was slowly poured onto the silica material over a period of about 2 minutes. Sirring was continued for another 5 minutes at low speed. The resulting product was a free flowing particulate material having a nonionic loading of 68% by weight.
Example 13 The procedure of Example 12 was repeated using a particulate silica material available under the trademark Quso. Quso is a precipitated silica having a surface area of 325 m'lgram and a 5% water content. The resulting product was a free flowing particulate material having a nonionic loading of 68% by weight.
Example 14 The procedure of Example 12 was repeated using a particulate silica material available under the trademark Syloid 244. Syloid 244 is a low density silica gel. The resulting product is a free flowing particulate material having a nonionic loading of 68% by weight.
Runs similar to Examples l-l4 can be made using liquid nonionic surfactants having a longer alkyl chain than Neodol 45-ll, i.e. 16-18 carbon atoms, and a higher ethylene oxide content, i.e. an average of 19 ethylene oxide units. A suitable liquid nonionic meeting these requirements is available from the Continental Oil Company under the trademark Alfonic 1618-78. It was found that, Alfonic l6l8-78 can be solidified with less effort, i.e. in less time, than Neodol 45-11 and to approximately the same loadings.
Functional carriers that can be heavily loaded with nonionic surfactants and still remain free flowing, noncaking powders were found to include pyrogenic silicon dioxide, which functions as an anti-caking agent in the final formulation, and various detergent builders such as NTA, sodium carbonate and sodium citrate.
When it is desired to incorporate a peroxygen bleach component into the detergent formulation, in addition to a nonionic surfactant component, it has been found that sodium perborate monohydrate is a surprisingly 'dTc'an'ie'r for the nonionic component since both can thereby be added in one post addition operation. Further, the addition of a small amount of pyrogenic silicon dioxide to mixtures of liquid nonionic surfactant and carrier material have been found to significantly increase the nonionic loadings of the post addable mixture while still retaining the necessary free flowing characteristics.
Although phosphate detergent builders have also been found to be very suitable carriers for liquid nonionic surfactants, their use is not preferred at this time because of the alleged contribution of phosphates to the eutrophication process in natural bodies of water. However, in reduced phosphate content detergent formulations, all or part of the phosphate builder can be added to the formulation subsequent to spray drying as a carrier for nonionic surfactants. In this regard, it has been found that phosphate builders, such as the sodium tripolyphosphate can be loaded with up to about 30 percent by weight liquid nonionic surfactant while still retaining free flowing properties. In accordance with the invention the nonionic loading on phosphate carriers can be increased to about 50 percent by weight by adding about 5 percent by weight of a microsized silica substance to the nonionic-carrier mixture before final setting.
By providing a commercially feasible method for post adding liquid nonionic surfactants to spray dried detergent formulations, the invention represents a significant step towards the substantial reduction of phosphate builders from detergent formulations without a significant decrease in cleaning efficacy.
Although the foregoing specific embodiments are presently preferred, they should not be considered as limiting the invention. Accordingly reference should be made to the following claims to determine the full scope of the invention.
We claim:
1. 1n the method of preparing a heavy duty detergent which includes the step of spray drying a detergent slurry to form a dry, free flowing powder, the improvement comprising adding to said spray dried powder a free flowing premix consisting of from 62 to 85 percent by weight of a liquid nonionic surface active agent chosen from the group consisting of ethoxylated alcohols having a 12 to 18 carbon atom chain and an average of from 10 to 19 ethylene oxide units and at least 5% by weight of microsized silica particles, said premix being prepared by mixing said liquid nonionic with a sufficient quantity of silica particles to fully solidify said liquid nonionic.
2. The improved method of claim 1, wherein said premix contains from about 65 to about by weight of said nonionic.
3. The improved method of claim 1, wherein said micro-sized silica particles are chosen from the group consisting of silica gels, silica aerogels, precipitated silicas and pyrogenic silicas.
4. The free flowing particulate product produced by the method of claim 1.
* t i i
Claims (4)
1. IN THE METHOD OF PREPARING A HEAY DUTTY DETERGENT WHICH INCLUDES THE STEPS OF SPRAY DRYING A DETERGENT SLURRY TO FORM A DRY, FREE FLOWERING POWDER, THE IMPROVEMENT COMPRISING ADDING TO SAID SPRAY DRIED POWDER A FREE FLOWING PREMIX CONSISTING OF FROM 62 TO 85 PERCENT BY WEIGHT OF A LIQUID NONIONIC SURFACE ACTIVE AGENT CHOSEN FROM THE GROUP CONSISTING OF ETHOXYLATED ALCHOLAS HAVING A 12 TO 18 CARBON ATOM CHAIN AND AN AVERAGE OF FROM 10 TO 19 ETHYLENE OXIDE UNITS AND AT LEAST 5% BY WEIGHT OF MICROSIZED PARTICLES, SAID PREMIX BEING PREPARED BY MIXING SAID LIQUID NONIONIC WITH A SUFFICIENT QUALITY OF SILICA PARTICLES TO FULLY SOLIDIFY SAID LIQUID NONIONIC.
2. The improved method of claim 1, wherein said premix contains from about 65 to about 75% by weight of said nonionic.
3. The improved method of claim 1, wherein said micro-sized silica particles are chosen from the group consisting of silica gels, silica aerogels, precipitated silicas and pyrogenic silicas.
4. The free flowing particulate product produced by the method of claim 1.
Priority Applications (10)
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GB442272A GB1369352A (en) | 1971-02-09 | 1972-01-31 | Free flowing nonionic surfactants |
DE2204842A DE2204842C2 (en) | 1971-02-09 | 1972-02-02 | Free-flowing non-ionic premix and its use in heavy duty detergents |
CA133,787A CA971071A (en) | 1971-02-09 | 1972-02-02 | Free flowing nonionic surfactants |
CH171472A CH567569A5 (en) | 1971-02-09 | 1972-02-07 | |
AU38759/72A AU464206B2 (en) | 1971-02-09 | 1972-02-07 | Freeflowing nonionic surfactants |
FR7203954A FR2124523B1 (en) | 1971-02-09 | 1972-02-07 | |
AT99672*#A AT335026B (en) | 1971-02-09 | 1972-02-08 | GIVING PREMIXES FOR ADDITIONAL ADDITION TO COARSE DETERGENTS |
NLAANVRAGE7201725,A NL178263B (en) | 1971-02-09 | 1972-02-09 | METHOD FOR PREPARING A PARTICULATE CLEANING AGENT |
US335873A US3915878A (en) | 1971-02-09 | 1973-02-26 | Free flowing nonionic surfactants |
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US4661358A (en) * | 1985-08-23 | 1987-04-28 | Quali Tech, Inc. | Wort-sequestered divalent metal salts |
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US4919847A (en) * | 1988-06-03 | 1990-04-24 | Colgate Palmolive Co. | Process for manufacturing particulate detergent composition directly from in situ produced anionic detergent salt |
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US5496486A (en) * | 1994-06-30 | 1996-03-05 | Amway Corporation | Process for increasing liquid surfactant loading in free flowing powder detergents |
US5714451A (en) * | 1996-03-15 | 1998-02-03 | Amway Corporation | Powder detergent composition and method of making |
AU2075097A (en) * | 1996-03-15 | 1997-10-01 | Amway Corporation | Discrete whitening agent particles, method of making, and powder detergent containing same |
AU2074397A (en) * | 1996-03-15 | 1997-10-01 | Amway Corporation | Powder detergent composition having improved solubility |
US5714450A (en) * | 1996-03-15 | 1998-02-03 | Amway Corporation | Detergent composition containing discrete whitening agent particles |
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EP3743495A1 (en) | 2018-01-26 | 2020-12-02 | Ecolab USA Inc. | Solidifying liquid amine oxide, betaine, and/or sultaine surfactants with a carrier |
JP7404245B2 (en) | 2018-01-26 | 2023-12-25 | エコラボ ユーエスエー インコーポレイティド | Solidification of liquid amine oxide, betaine, and/or sultaine surfactants using binders and optional carriers |
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US4076643A (en) * | 1973-11-09 | 1978-02-28 | Solvay & Cie. | Pre-mixes intended to be added to detergent powders by post-addition |
US4064063A (en) * | 1974-07-01 | 1977-12-20 | Henkel Kommanditgesellschaft Auf Aktien | Process for the manufacture of spray dried detergents containing nonionic tensides |
US4125475A (en) * | 1974-12-23 | 1978-11-14 | Texaco Inc. | Detergents containing a fatty alcohol builder and a water-insoluble inorganic absorbent |
US4263050A (en) * | 1975-04-30 | 1981-04-21 | Kao Soap Co., Ltd. | Process for preparation of granules containing viscous substance at high concentration |
US4663194A (en) * | 1976-12-02 | 1987-05-05 | The Colgate-Palmolive Co. | Phosphate-free concentrated particulate heavy duty laundry detergent |
US4666740A (en) * | 1976-12-02 | 1987-05-19 | The Colgate-Palmolive Co. | Phosphate-free concentrated particulate heavy duty laundry detergent |
US4260651A (en) * | 1976-12-02 | 1981-04-07 | Colgate-Palmolive Company | Phosphate-free concentrated particulate heavy duty laundry detergent |
US4339335A (en) * | 1976-12-02 | 1982-07-13 | Colgate Palmolive Co. | Free flowing high bulk density particulate detergent-softener |
US4347152A (en) * | 1976-12-02 | 1982-08-31 | Colgate-Palmolive Company | Phosphate-free concentrated particulate heavy duty laundry detergent |
US4411809A (en) * | 1976-12-02 | 1983-10-25 | Colgate Palmolive Company | Concentrated heavy duty particulate laundry detergent |
DK152294B (en) * | 1976-12-02 | 1988-02-15 | Colgate Palmolive Co | Free-flowing, PHOSPHATE-FREE PARTICULATE, POWERFUL EFFECTIVE DETERGENT |
DK152588B (en) * | 1976-12-02 | 1988-03-21 | Colgate Palmolive Co | Free-flowing, particulate, powerfully effective detergent |
US4248911A (en) * | 1976-12-02 | 1981-02-03 | Colgate-Palmolive Company | Concentrated heavy duty particulate laundry detergent |
US4190551A (en) * | 1977-06-14 | 1980-02-26 | Kao Soap Co., Ltd. | Granular or powdery detergent composition of high fluidity |
DE2753680A1 (en) * | 1977-12-02 | 1979-06-07 | Henkel Kgaa | PROCESS FOR THE PRODUCTION OF POWDERED DETERGENTS CONTAINING ORGANIC SILICON POLYMERS WITH IMPROVED SOLUTION PROPERTIES |
US4664817A (en) * | 1980-03-27 | 1987-05-12 | The Colgate-Palmolive Co. | Free flowing high bulk density particulate detergent-softener |
US4664950A (en) * | 1980-09-02 | 1987-05-12 | The Colgate Palmolive Co. | Concentrated heavy duty particulate laundry detergent |
US4666738A (en) * | 1980-09-02 | 1987-05-19 | The Colgate-Palmolive Co. | Method for making a phosphate containing concentrated heavy duty particulate laundry detergent |
US4473485A (en) * | 1982-11-05 | 1984-09-25 | Lever Brothers Company | Free-flowing detergent powders |
US4741851A (en) * | 1984-04-02 | 1988-05-03 | Colgate Palmolive Co. | Non-caking bleaching detergent composition containing a lower hydrate of sodium perborate |
US4695284A (en) * | 1984-06-15 | 1987-09-22 | Lever Brothers Company | Cool water fabric washing process using a particulate detergent containing a nonionic and a fatty acid builder salt |
US4908159A (en) * | 1985-05-10 | 1990-03-13 | Lever Brothers Company | Detergent granules containing simple sugars and a seed crystal for calcium carbonate |
US4857223A (en) * | 1985-10-03 | 1989-08-15 | Colgate-Palmolive Company | Non-caking bleaching detergent composition containing a lower hydrate of sodium perborate |
US5354493A (en) * | 1988-10-21 | 1994-10-11 | Henkel Kommanditgesellschaft Auf Aktien | Process for the production of surfactant-containing granulates |
US5064562A (en) * | 1989-10-09 | 1991-11-12 | Rhone-Poulenc Chimie | Stable pumpable zeolite/silicone suspensions |
EP0477974A2 (en) * | 1990-09-28 | 1992-04-01 | Kao Corporation | Nonionic powdery detergent composition |
EP0477974A3 (en) * | 1990-09-28 | 1992-10-21 | Kao Corporation | Nonionic powdery detergent composition |
US5705473A (en) * | 1990-09-28 | 1998-01-06 | Kao Corporation | Nonionic powdery detergent composition containing an aluminosilicate builder and a silicon-containing oil absorbing carrier |
WO1993004162A1 (en) * | 1991-08-20 | 1993-03-04 | Henkel Kommanditgesellschaft Auf Aktien | Method of producing granular surfactant material |
US5516447A (en) * | 1991-08-20 | 1996-05-14 | Henkel Kommanditgesellschaft Auf Aktien | Method of producing granular surfactants |
US5654265A (en) * | 1992-03-12 | 1997-08-05 | Kao Corporation | Nonionic powdery detergent composition |
EP0637628A2 (en) * | 1993-08-03 | 1995-02-08 | Amway Corporation | Mix process for formulating detergents |
EP0637628A3 (en) * | 1993-08-03 | 1998-03-11 | Amway Corporation | Mix process for formulating detergents |
US6174852B1 (en) * | 1996-01-22 | 2001-01-16 | Kao Corporation | High-density powdered detergent composition |
US6303558B1 (en) | 1997-05-30 | 2001-10-16 | Lever Brothers Co., Division Of Conopco | Detergent composition containing at least two granular components |
US20040029765A1 (en) * | 2001-02-07 | 2004-02-12 | Henriette Weber | Washing and cleaning agents comprising fine microparticles with cleaning agent components |
US7601678B2 (en) * | 2001-02-07 | 2009-10-13 | Henkel Ag & Co. Kgaa | Washing and cleaning agents comprising fine microparticles with cleaning agent components |
US20090137449A1 (en) * | 2005-04-22 | 2009-05-28 | Thomas Holderbaum | Washing or cleaning agent |
US20100180388A1 (en) * | 2007-07-20 | 2010-07-22 | Heike Schirmer-Ditze | Ironing Pad Comprising a Solid Stain Treatment Composition |
WO2021043999A1 (en) | 2019-09-06 | 2021-03-11 | Basf Se | Solid surfactant compositions |
Also Published As
Publication number | Publication date |
---|---|
AU464206B2 (en) | 1975-08-01 |
NL7201725A (en) | 1972-08-11 |
FR2124523B1 (en) | 1976-07-30 |
AU3875972A (en) | 1973-08-09 |
CA971071A (en) | 1975-07-15 |
GB1369352A (en) | 1974-10-02 |
DE2204842C2 (en) | 1987-11-12 |
AT335026B (en) | 1977-02-25 |
US3769222A (en) | 1973-10-30 |
NL178263B (en) | 1985-09-16 |
FR2124523A1 (en) | 1972-09-22 |
DE2204842A1 (en) | 1972-08-24 |
CH567569A5 (en) | 1975-10-15 |
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