US2298650A - Particulate detergent composition - Google Patents
Particulate detergent composition Download PDFInfo
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- US2298650A US2298650A US336716A US33671640A US2298650A US 2298650 A US2298650 A US 2298650A US 336716 A US336716 A US 336716A US 33671640 A US33671640 A US 33671640A US 2298650 A US2298650 A US 2298650A
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- United States
- Prior art keywords
- detergent
- parts
- sodium sulfate
- mesh
- particulate
- Prior art date
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- 239000000203 mixture Substances 0.000 title description 57
- 239000003599 detergent Substances 0.000 title description 43
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 31
- 229910052938 sodium sulfate Inorganic materials 0.000 description 29
- 235000011152 sodium sulphate Nutrition 0.000 description 29
- 239000007787 solid Substances 0.000 description 26
- 239000000047 product Substances 0.000 description 25
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 22
- 239000000470 constituent Substances 0.000 description 19
- 239000002245 particle Substances 0.000 description 18
- 230000005484 gravity Effects 0.000 description 16
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 15
- -1 alkylated aromatic sulfonic acids Chemical class 0.000 description 14
- 150000003839 salts Chemical class 0.000 description 13
- 238000001694 spray drying Methods 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 12
- 239000007864 aqueous solution Substances 0.000 description 12
- 239000007789 gas Substances 0.000 description 12
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 11
- 235000019341 magnesium sulphate Nutrition 0.000 description 11
- 239000000725 suspension Substances 0.000 description 10
- 239000007900 aqueous suspension Substances 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 7
- 238000001035 drying Methods 0.000 description 7
- 239000013042 solid detergent Substances 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical class CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 235000017550 sodium carbonate Nutrition 0.000 description 6
- 229940001593 sodium carbonate Drugs 0.000 description 6
- 229910000029 sodium carbonate Inorganic materials 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- 229910052783 alkali metal Inorganic materials 0.000 description 5
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 230000000717 retained effect Effects 0.000 description 5
- JHJUUEHSAZXEEO-UHFFFAOYSA-M sodium;4-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=C(S([O-])(=O)=O)C=C1 JHJUUEHSAZXEEO-UHFFFAOYSA-M 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 150000001555 benzenes Chemical class 0.000 description 4
- 150000008107 benzenesulfonic acids Chemical class 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- 238000009736 wetting Methods 0.000 description 3
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 229910021538 borax Inorganic materials 0.000 description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 230000007717 exclusion Effects 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 235000010339 sodium tetraborate Nutrition 0.000 description 2
- 239000004328 sodium tetraborate Substances 0.000 description 2
- 239000008096 xylene Chemical class 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical class [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical class CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- SQEDZTDNVYVPQL-UHFFFAOYSA-N dodecylbenzene;sodium Chemical compound [Na].CCCCCCCCCCCCC1=CC=CC=C1 SQEDZTDNVYVPQL-UHFFFAOYSA-N 0.000 description 1
- 238000004836 empirical method Methods 0.000 description 1
- 239000012527 feed solution Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Chemical class 0.000 description 1
- 239000002184 metal Chemical class 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000011780 sodium chloride 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
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- MZSDGDXXBZSFTG-UHFFFAOYSA-M sodium;benzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=CC=C1 MZSDGDXXBZSFTG-UHFFFAOYSA-M 0.000 description 1
- 239000008234 soft water Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 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
- C11D11/02—Preparation in the form of powder by spray drying
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
-
- 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/06—Powder; Flakes; Free-flowing mixtures; Sheets
-
- 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
- C11D3/04—Water-soluble compounds
- C11D3/046—Salts
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
- Y10S516/03—Organic sulfoxy compound containing
Definitions
- the present invention relates'to new particulate detergent compositions which are free-flowassignors to Monsanto Chemical H Company, St. Louis, Mo., a corporation of Delav I gund substantially non-hygroscopic and noncaking. a Many of the commercial preparations of detergent compositions, and in particular detergent compositions comprising water-soluble salts of alkylated aromatic sulfonic acids, exhibit the un desirable property of wetting down on exposure to the atmosphere. Such caking or wetting down of the detergent composition is of such inconvenience and undesirability as to substantially preclude their commercial .use.
- the improved particulate detergent compositions of the present invention are not substantially ailected by atmospheric moisture and as a result retain their particulate form when subjected to conditions which produce melting and caking of other particulate detergent compositions.
- the principal object of the present invention is to provide a detergent composition in particulate form which shall be characterized by especially high detergent efiiciency and which shall dissolve rapidly in water, be substantially unaffected by atmospheric moisture conditions norvmally prevailing in different geographical localities, and which shall be substantially free of fine particles that are readily borne by circulating air currents in the home and substantially free from any tendency to disintegrate into finer particles on standing or shaking.
- the detergent composition shall be of stable particulate form, have a low apparent specific gravity and be free from fine dust particles and shall be stable and free pheric conditions.
- a detergent composition conforming in a-remarkable degree to the specifications outlined in the foregoing object can be made by spray-drying an aqueous solution or a uniunder prevailing atrnosform or homogeneous suspens on compr sing S5 dium sulfate and certain alkylated aromatic drgc arbon sulfonic acid salts which are specified hereinafter.
- the ratio of sodium sulfate to the salt of the alkylated ar o matic hydrocarbon sulfonic acid may be varied widely provided at least approximately 20% sodium sulfate is present, but compositionshaving optimum non-caking characteristics and detergent efilciency andwhich are at the same time of low apparent specific gravity and free irom tendency to disintegrate are those comprising 20% to 80% sodium sulfate and preferably 35% to while the content of alkylated aromatic sulfonic acid salt is to 20% and preferably 65% to 35%.
- Sodium sulfate may be replaced by sodium carbonate in such compositions up'to about 50% or. more of the detergentbuilder content (see, for example Detergent Mix B hereinafter) with but slight changes in general characteristics but with significant changes in the alkalinity of the detergent composition, that is, a detergent of this class containing sodium carbonate is slightly alkaline but one containing only sodium sulfate as the constituent other than the alkylated aromatic hydrocarpon s lfonic acid salt is approximately neutral in reation.
- some of the sodium sulfate may be replaced by billlfilfsiflsllch as tetrasodium pyrophosphate, borax and the like.
- the composition should not be dried to the total exclusion oi. moisture. ulate' pi from approximately iomssfoa eii'l By ob'iViifithese limits undesirable fragmentation or disintegration into fine powder is inhibited and the tendency to produce dust or undesirable f H fines on standing or shaking is eliminated.
- Com- V positions which have been dried to the exclusion of all moisture have a tendency to absorb moisture, which absorption may be accompanied by disintegration of the original particles.
- solid composition should have a moisture cgn ten 60% relative humidity. drying aqueous solutions or homogeneous susbut that the moisture content of the final product must also be controlled since the combined moisture has a binding or cohesive effect on the individual particles and prevents absorption or liberation of substantial proportions of moisture D which are accompanied by disintegration or crumbling of the particles.
- the low apparent specific gravity of the product is also of importance since the particles are blown up" or hollow and this indirectly is connected with the tendency of the 1 particles to absorb and liberate water without wetting down and caking and without disintegration or crumbling oi. the individual particles.
- Particulate detergents of this type having a lower apparent specific gravity than 0.05 are unstable, 1 friable. and disintegrate on standing into finer particles and dust. Particulate detergents such that substantially all particles are retained on an BO-mesh sieve are preferred.
- salts ot. al kylatcd. aromatic lhydrocarbonnz sulfonicaacids which are contemplated for use in this invention are water-soluble, particularly alkali-metal, salts of alkylated benzene sulfonic acids in which at least one alkyl group contains exposed for varied periods to atmospheres having a relative humidity of 60% or more.
- the composition made with sodium sulfate in this manner retained its particulate form, was freeflowing, and was dry in appearance after six days.
- sodium silicate is unique in that it enhances the detergent activity of the composition and has a most desirable eiiect on the physical characteristics of the resulting spray-dried product.
- the sodium sulfate is present in the product in a form analogous to the beta form of anhydrous sodium sulfate and that in the product the alkali-metal salt of the alkylated aromatic hydrocarbon sulfonic acid prevents transformation of the beta form to the alpha form. It is known (see J. W. Mellor, "A Comprehensive Treatise on Inorganic and Theoretical Chemistry, London, Longmans, Green 00., vol. II, 1927, page 661) that the beta form of anhydrous sodium sulfate does not hydrate while the alpha form combines immediately with water at 25 and-that hydration of the beta form starts only when it has passed into the alpha form.
- any suitable apparatus and method of spraydrying aqueous solutions or suspensions of the alkylated b epgge e sulinnate and sodium sulfate This?HE'used provided the process is adjusted to obtain a particulate product having an apparent specific gravity within the range of 0.05 to 0.25 and a moisture content of 1.0% to 5.0% and a desired uniform particle size (80 mesh screen or thereabout)
- Methods and apparatus for spraydrying are described in the articles by W. S. Bowen in Ind. Eng. Chem., 1938, vol. 30, page 1001-2 and Ben B. Fogler and Robert W.
- the system is adjusted so that a powder the individual particles of which are of such size that the powder is almost completely retained on an -mesh sieve is obtained.
- the invention is not limited to an specific method of spray-drying whereby a product of this character is obtained.
- a spraydrying unit of conventional type consisting of a chamber provided with a hopper at the bottom, an inlet for heated gases, and an outlet for exhaust gases, an inlet for feeding heated solutions or suspensions of the composition to be dried, and a disc spray wheel driven by a, variable speed electric motor and capable of rotating at a speed of 6000 R. P. M. or greater has been used for this purpose. Subdivision of the solution or.
- suspension is effected on the spray wheel itself andby the centrifugal, force 2,298,650 g I 3 of the wheel when in motion.
- Ilze drying cham xle rsgi; tower into which the subdivi e so ution pension is passed is heated by means of hot air introduced by suitable means atthe top of the tower and circulated from the top to the bottom thereof, from which point the cooled air passes through an outlet together with an finely divided solids into "additional towers and finally through water sprays to remove all solids remaining in the exit gases.
- cold air may be introduced preferably at the bottom of the tower to reduce the temperature of both the exit gases and the condensed solid.
- any changes in the temperature of the exit gases is an indication that some other part of the system is not operating properly, hence checking should be instituted and compensation should be made therefor by changing the temperature of the feed solution or suspension or the feed rate, by changing the volume or temperature of the inlet gases or by admitting cooler air, or by speeding up or slowing down the disc sprayer although this latter factor is more directly connected with the size and character of the particles than with'their dryness.
- sodium sulfate and alkali-metal salt of the alkylated aromatic hydrocarbon sulfonic acid be present in solution before drying or be in the form of a-homogenous uniform suspension or slurry; otherwise products which cake in masses throughout the batch are likely to result. 4
- the products of the foregoing examples were all free-flowing, dry powders which retained their free-flowing character after exposure for six days to atmospheres having humidities of 60%, 85% and 93%.
- the percentage moisture absorbed in such humidity tests are exemplified in the results reported for the products of Example 2.
- the test is performed as follows:. Definite weighed portions of the detergent under test were placed in open containers which in turn were placed in jars containing saturated aqueous solutions of appropriate inorganic salts in contact with an excess of the solid phase chosen so as to produce 60%, 85% and 93% relative humidities.
- the jars containing the detergent were then tightly closed and allowed to stand for six days, at the end of which time they were opened and the condition of the detergent noted as to increase in Weight and whether or not it had caked or remained free-flowing.
- the character of the product is of greater significance than the percentage moisture absorbed since other materials which have absorbed the same amount of moisture may be entirely Wetted and caked.
- the sieve test used is similar to that of the A. S. T. M. and represents the relative content and varying size of the different particles of the composition.
- the screen tests of several commercial detergent compositions obtained in the market were as follows:
- OnBOmesh 17.6 15.1 19.7 22.7 On 100 mesh... 54.4 7.8 7.5 7.8 On 150 mcsh. 14.0 3.1 1.2 1.6 On 200mcsh. 4.8 0.8 0.4 0.4 Through 200 mesh 4.8 0.8 0.4 0.4 Loss 3. 6
- compositions for use according to this invention are such as contain 40% active alkylated aromatic hydrocarbon sulfonate.
- Such compositions are, for example, represented by Detergent Mix C or by the following compositions, which can be spray-dried according to the method disclosed herein. All proportions stated are in parts by weight of anhydrous materials.
- the diethylene glycol which is present in the compositions of Examples VI and VII is used to prevent dusting of any fine particles originally formed as a result of imperfect control of particle size in'the spray-drying operation. It may be replaced by glycerol or similar material to entirely omitted.
- Examples VI and VII which contain a smaller added proportion of magnesium sulfate than other disclosed products are particularly suitable for preparations made by dissolving or homogeneously suspending the materials in water containing some original hardness.
- the hardness of the water, representing magnesium and other metal salts, will be found in the final spray-dried product.
- the water used for this purpose is soft or distilled water a greater proportion of magnesium sulfate will be required to com-u.
- pensate for the magnesium salts that are absent from the water Generally from about 0.5 to
- magnesium sulfate anhydrous basis
- a substantially uniform non-cakingfreeflowing, particulate detergent composition can be obtained, which is not the case when the watersoluble salt of the aromatic hydrocarbon sulionic acid is dried in a mass and mechanically mixed with sodium sulfate or when a solution of the aromatic hydrocarbon sulfonic acid salt and sodium sulfate in indiscriminate proportions is dried in a mass and then disintegrated mechanically by grinding.
- Uniformity of'particle size cannot be controlled mechanically nor can the caking characteristics be controlled by purely empirical methods. as is evident from the foregoing description.
- a non-caking, free-fiowing particulate solid detergent composition having an apparent specific gravity of about 0.05 to 0.25 and a moisture content of about 1.0 to 5.0% obtained by spraydrying an aqueous solution or homogeneous aqueous suspension, the solid constituents of which comprise a mixture of 35 to 65 parts by weight ofsodiuin sulfate and 65 to 35 parts by weight of a water-soluble salt of a monoalkyl-substituted aromatic hydrocarbon sulfonic acid selected from the group consisting of water-soluble salts of monoalkyl-substituted benzene, toluene and xylene sulfonic acids, the substituted alkyl groups of which contain at least 11 and less than 16 1.
- a non-caking, free-flowing particulate solid detergent composition of which substantially all the individual particles thereof are retained on an Bil-mesh sieve and which has an apparent 16 carbon atoms, to each 100 parts by weight of the solid constituents.
- a non-caking, free-flowing particulate solid detergent composition having an apparent specific gravity of about 0.05 to 0.25 and a moisture content of about 1.0 to 5.0% obtained by spray- ,drying an aqueous solution or homogeneous aqueous suspension, the solid constituents of which comprise a mixture of 35 to 65 parts by weight of sodium sulfate and 65 to 35 parts by weight of an alkali-metal salt of a monOalkylated benzene sulfonic acid, the alkyl group oi? which contains at least 11 and less than 16 carbon atoms, to each 100 parts by weight of the solid constituents.
- a non-calcing, free-flowing particulate solid detergent composition having an apparent specific gravity of about 0.05 to 0.25 and a moisture content of about 1.0 to 5.0% obtained by spraydrying an aqueous solution or homogeneous aqueous suspension, the solid constituents of which comprise a mixture of 35 to 65 parts by weight of sodium sulfate and'65 to 35 parts by i weight of a sodium salt of a monoallclated benzene sulfonic acid, the alkyl group of which contains at least 11 and less than 16 carbon atoms,
- a non-caking, free-flowing particulate solid alkylated benzene sulfonic acids the alkyl groups of which contain at least 11 and less than 16 carbon atoms, to each 100 parts by weight of the solid constituents.
- a non-caking, free-flowing articulate solid detergent composition having an apparent specific gravity of about 0.05 to 0.25 and a moisture content of about 1.0 to 5.0% obtained by spraydrying an aqueous solution or homogeneous 19 aqueous suspension, the solid constituents of which comprise the following substances in approximately the following proportions by weight: 60 parts of sodium sulfate and 40 parts of sodium salts of a mixture of monoalkylated benzene sulfonic acids, the alkylgroups of which contain at least 11 and less than 16 carbon atoms, to each 100 parts of the solid constituents.
- a non-caking, free fiowing particulate solid detergent composition having an apparent specontent of about 1.0 to 5.0% obtained by spraycific grayity of about 0.05 to 0.25 and a moisture drying an aqueous solution or homogeneous aqueous suspension, the solid constituents of whichcomprise the following substances in approximately the following proportions by weight: 36 parts of sodium sulfate, 24 partfof sodium carbonate and 40 parts of sodium salts of a mixture of monoalkylated benzene suifonic acids, the alkyl groups of which contain at least 11 and less than 16 carbon atoms, to each 100 parts of the solid constituents.
- a non-casing, free-flowing particulate solid ent composition having an apparent spe- .1
- cific gravity of about 0.05 to 0.25 and a moisture content of about 1.0 to 5.0% obtained by spraydrying an aqueous solution or homogeneous aqueous suspension, the solid constituents of which comprise the following substances in approximately the iollowing proportions by weight: 58.5 parts of sodium sulfate, 40 parts of dodecylbenzene sodium sulfonate and 0.5 part of magnesium sulfate (anhydrous basis), to each 99 parts of the solid constituents.
- a non-calling, free-flowing particulate solid 43 detergent composition having an apparent specific gravity of about 0.05 to 0.25 and a moisture content of about 1.0 to 5.0% obtained by spraydrying an aqueous solution or homogeneous aqueous suspension, the solid constituents 01 which comprise the following substances in ap proximately the following proportions by weight: 58.5 parts of sodium sulfate, 40 parts of dodecylbenzene sodium sulfonate and 0.5 part of diethylene glycol, to each 99 parts of the solid constituents.
- NICHOLAS N 1. SAHARAS, ET AL,
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- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
Description
1 from caking tendency aiente'd Oct. 13, 1942 Nicholas N. T. Dayton, Ohio,
ware
.. No Drawing. Appliqation' May 23, 1940, my
1 p asssnie Claims. (01. 252- 54;) 2 m The present invention relates'to new particulate detergent compositions which are free-flowassignors to Monsanto Chemical H Company, St. Louis, Mo., a corporation of Delav I gund substantially non-hygroscopic and noncaking. a Many of the commercial preparations of detergent compositions, and in particular detergent compositions comprising water-soluble salts of alkylated aromatic sulfonic acids, exhibit the un desirable property of wetting down on exposure to the atmosphere. Such caking or wetting down of the detergent composition is of such inconvenience and undesirability as to substantially preclude their commercial .use. The improved particulate detergent compositions of the present invention are not substantially ailected by atmospheric moisture and as a result retain their particulate form when subjected to conditions which produce melting and caking of other particulate detergent compositions.
The present application is a continuation-inpart of our co-pending application Serial No. 183,509, filed January 5, 1938.
The principal object of the present invention is to provide a detergent composition in particulate form which shall be characterized by especially high detergent efiiciency and which shall dissolve rapidly in water, be substantially unaffected by atmospheric moisture conditions norvmally prevailing in different geographical localities, and which shall be substantially free of fine particles that are readily borne by circulating air currents in the home and substantially free from any tendency to disintegrate into finer particles on standing or shaking. The detergent composition shall be of stable particulate form, have a low apparent specific gravity and be free from fine dust particles and shall be stable and free pheric conditions.
In accordance with the present invention it has been discovered that a detergent composition conforming in a-remarkable degree to the specifications outlined in the foregoing object can be made by spray-drying an aqueous solution or a uniunder prevailing atrnosform or homogeneous suspens on compr sing S5 dium sulfate and certain alkylated aromatic drgc arbon sulfonic acid salts which are specified hereinafter. By observing certain ratios of constituents and conducting the drying in such a manner as to leave a determinate moisture content in the product, free-flowing relatively nonf hygroscopic particulate detergent compositions having an apparent specific gravity within the range of 0.05 to 0.25 are obtained.
, The ratio of sodium sulfate to the salt of the alkylated ar o matic hydrocarbon sulfonic acid may be varied widely provided at least approximately 20% sodium sulfate is present, but compositionshaving optimum non-caking characteristics and detergent efilciency andwhich are at the same time of low apparent specific gravity and free irom tendency to disintegrate are those comprising 20% to 80% sodium sulfate and preferably 35% to while the content of alkylated aromatic sulfonic acid salt is to 20% and preferably 65% to 35%. v Small proportions of additional detergent builders such as magnesium sulfate may be present without changing the properties of the composition substantially.- Sodium sulfate may be replaced by sodium carbonate in such compositions up'to about 50% or. more of the detergentbuilder content (see, for example Detergent Mix B hereinafter) with but slight changes in general characteristics but with significant changes in the alkalinity of the detergent composition, that is, a detergent of this class containing sodium carbonate is slightly alkaline but one containing only sodium sulfate as the constituent other than the alkylated aromatic hydrocarpon s lfonic acid salt is approximately neutral in reation. Similarly, some of the sodium sulfate may be replaced by billlfilfsiflsllch as tetrasodium pyrophosphate, borax and the like. V v
In the preparation of the detergent composltion, the composition should not be dried to the total exclusion oi. moisture. ulate' pi from approximately iomssfoa eii'l By ob'iViifithese limits undesirable fragmentation or disintegration into fine powder is inhibited and the tendency to produce dust or undesirable f H fines on standing or shaking is eliminated. Com- V positions which have been dried to the exclusion of all moisture have a tendency to absorb moisture, which absorption may be accompanied by disintegration of the original particles. 1 Greater proportions of combined'moisture when present in the product may produce liberation of moisture from the product underatmospheric conditions prevailing in certain localities, as a result of which disintegration and dusting oi" the particles together with localized caking oi the entire bulk islikelytooccur. i I i I The invention involves the discovery not only that certain specific proportions of sodium sulfate and the alkylated aromatic hydrocarbon sulfonic acid salt must be observed to obtain a par- I ticulate product which on spray-drying will be if substantially stable, free-flowing and non-wiring,
solid composition should have a moisture cgn ten 60% relative humidity. drying aqueous solutions or homogeneous susbut that the moisture content of the final product must also be controlled since the combined moisture has a binding or cohesive effect on the individual particles and prevents absorption or liberation of substantial proportions of moisture D which are accompanied by disintegration or crumbling of the particles. The low apparent specific gravity of the product is also of importance since the particles are blown up" or hollow and this indirectly is connected with the tendency of the 1 particles to absorb and liberate water without wetting down and caking and without disintegration or crumbling oi. the individual particles. Particulate detergents of this type having a lower apparent specific gravity than 0.05 are unstable, 1 friable. and disintegrate on standing into finer particles and dust. Particulate detergents such that substantially all particles are retained on an BO-mesh sieve are preferred.
'ghe salts ot. al kylatcd. aromatic lhydrocarbonnz sulfonicaacids which are contemplated for use in this invention are water-soluble, particularly alkali-metal, salts of alkylated benzene sulfonic acids in which at least one alkyl group contains exposed for varied periods to atmospheres having a relative humidity of 60% or more. The composition made with sodium sulfate in this manner retained its particulate form, was freeflowing, and was dry in appearance after six days. Compositions made with tetrasodiurn pyrophosphate, ,borax and sgiiugn ilicate respectiv'ly," in placeof the sodium sulfate, were caked at the end of six days, the silicate mixture being a solid mass. The percentages of moisture absorbed in the last three cases were from W 9....l..earbon aioms. .ana..silrs a sss dodecyl, tridecyl, tetradecyl and pentadecyl substituted benzene, toluene, xylene and similar aromatic hydrocarbons of the benzene series, 3 as well as their isomers and mixtures thereof,
are included within the ambit of the invention.
Heretoiore, in the manufacture of detergent compositions from water-soluble, metallic salts of alkylated aromatic sulfonic acids in which the alkyl group contains, more than 8 and less than 3.6 carbon atoms, great difliculty and inconvenience in handling were experienced because of the tendency of the materials tocake and deliquesce. Attempts to remedy or elirn- .4 inate this undesirable property of the products by the simple mechanical admixture of anhydrous sodium sulfate with the water-soluble alkali-metal salts of said allrylated aromatic sulfonic acids did not result in afree-flowing, non-hygroscopic solid. Similarly, on grinding, dodecyl benzene sodium sulfonate with an equal weight of a mixture of equal parts by weight of sodium chloride and sodium benzene monosulfonate, the powdered product caked to a semisolid after less than six days of exposure to However, on spraypensions of the alkylated aromatic sulfonate containing sodium sulfate, according to the present invention, the caking and deliquescing of the detergent is unexpectedly eliminated and the product possesses the other desirable properties referred to herein. a
not substantially difierent, although it was higher in all cases than that of the composition containing sodium sulfate, yet the degree and character of the caking was difierent and was most marked in the case of sodium silicate. The problem is obviously not solely one of moisture absorption alone. Furthermore, a great variety of salts which might otherwise appear useful for the purpose of preventing caking of the detergent compositions could not be used because of their adverse effect on the detergent characteristics of the composition. In this respect sodium sulfate is unique in that it enhances the detergent activity of the composition and has a most desirable eiiect on the physical characteristics of the resulting spray-dried product.
It is believed that under the conditions of drying specified in the present invention the sodium sulfate is present in the product in a form analogous to the beta form of anhydrous sodium sulfate and that in the product the alkali-metal salt of the alkylated aromatic hydrocarbon sulfonic acid prevents transformation of the beta form to the alpha form. It is known (see J. W. Mellor, "A Comprehensive Treatise on Inorganic and Theoretical Chemistry, London, Longmans, Green 00., vol. II, 1927, page 661) that the beta form of anhydrous sodium sulfate does not hydrate while the alpha form combines immediately with water at 25 and-that hydration of the beta form starts only when it has passed into the alpha form.
Any suitable apparatus and method of spraydrying aqueous solutions or suspensions of the alkylated b epgge e sulinnate and sodium sulfate This?HE'used provided the process is adjusted to obtain a particulate product having an apparent specific gravity within the range of 0.05 to 0.25 and a moisture content of 1.0% to 5.0% and a desired uniform particle size (80 mesh screen or thereabout) Methods and apparatus for spraydrying are described in the articles by W. S. Bowen in Ind. Eng. Chem., 1938, vol. 30, page 1001-2 and Ben B. Fogler and Robert W. Klein- A great variety of detergent compositions have been made with a mixture of dodecylflandatriem fl n aiastsiiiieaetesa an equal part by weight of sodium sulfate or other salt in eiIorts to produce a free-flowing non-casing and non-crumbling particulate detergent composition. These compositions were made by spraying aqueoussolutions or suspensions of the desired composition into a heated chamber, according to the method of the present invention. The dried particulate compositions were then schmidt, Ind. Eng. Chem., 1938, vol. 30, pages 1372-84. Preferably the system is adjusted so that a powder the individual particles of which are of such size that the powder is almost completely retained on an -mesh sieve is obtained. The invention is not limited to an specific method of spray-drying whereby a product of this character is obtained. However, a spraydrying unit of conventional type consisting of a chamber provided with a hopper at the bottom, an inlet for heated gases, and an outlet for exhaust gases, an inlet for feeding heated solutions or suspensions of the composition to be dried, and a disc spray wheel driven by a, variable speed electric motor and capable of rotating at a speed of 6000 R. P. M. or greater has been used for this purpose. Subdivision of the solution or. suspension is effected on the spray wheel itself andby the centrifugal, force 2,298,650 g I 3 of the wheel when in motion. Ilze drying cham xle rsgi; tower into which the subdivi e so ution pension is passed is heated by means of hot air introduced by suitable means atthe top of the tower and circulated from the top to the bottom thereof, from which point the cooled air passes through an outlet together with an finely divided solids into "additional towers and finally through water sprays to remove all solids remaining in the exit gases. If convenient or desirable, cold airmay be introduced preferably at the bottom of the tower to reduce the temperature of both the exit gases and the condensed solid.
By means of this type of equipment products conforming to the hereinabove described characteristics were obtained. Variations in characteristics within these limits can be obtained by changes in the temperature; concentration and rate of feed of the solution or suspension to be dried, speed of the rotatingspray disc, and temperature and volume of the inlet gases. A degree of control of the entire unit can be maintained by observation of the temperature of the outlet gases. When such a unit is operating to produce a determinate character of product, any changes in the temperature of the exit gases is an indication that some other part of the system is not operating properly, hence checking should be instituted and compensation should be made therefor by changing the temperature of the feed solution or suspension or the feed rate, by changing the volume or temperature of the inlet gases or by admitting cooler air, or by speeding up or slowing down the disc sprayer although this latter factor is more directly connected with the size and character of the particles than with'their dryness.
It is important that the sodium sulfate and alkali-metal salt of the alkylated aromatic hydrocarbon sulfonic acid be present in solution before drying or be in the form of a-homogenous uniform suspension or slurry; otherwise products which cake in masses throughout the batch are likely to result. 4
The following examples are illustrative of the invention and represent the results of operating in such a spray-drying unit under different operating conditions and the character of the products obtained. Inthese examplesthe solid detergent components of the feed stocks which were used were present in the following proportions in parts by weight: I Detergent Mix A I Magnesium sulfate (anhydrous Mg S04 basis) 2 Parts Exnrrrs I Operating conditions Feed stock -Q. 40% suspension of a V Detergent Mix A in water. J Temperature of feed stock 54 C. r I Inlet gas temperature 232 C. Outlet gas temperature 121 C. I Spray wheel type Small labyrinth type. Speed of spray wheel 3000 R. P. M.
I Product Apparent specific gravity 0.1330
Sieve test:
Percent On mesh 22.0
On 40 mesh 39.4 On 60 mesh 30.6 On 80 mesh 4.8 On 100 mesh 2.5 Through 100 mesh -p- 0.7
I; ExAiuPLEII Operating conditions Feed stock 50% suspension of Detergent Mia: B 1 r- Mixture of dodecyl and tridecyl benzene sodium sulfonates 100 g Sodium sulfate (anhydrous basis) 60 Sodium carbonate (anhydrous basis) 40 Magnesium sulfate (anhydrous Mg .804
basis) 2 Detergent M in: C
- v Detergent Mix 15. Temperature of feed stock 60 C. I
Six-day relative humidity tests:
Relative humidity 60% 85% 93% Per cent moisture absorbed- None 2.3 2.6
Sieve test: 1
- Per cent On 30 mesh 5.2 On 40 mesh 30.3 On 60 mesh 32.7 On 100 mesh 24.4 Through 100 mesh 6.6
I Exiiurrs III I Operating conditions 7 Feed stockQQ. Q.-. suspension of .,,DetergentMixA water.
' Temperature of feed stock- C.
Inlet gas temperature"--- 232 C.
Outlet gas temperature 121 C.
Spray wheel type Small labyrinth type Speed of spray wheel .3000 R. P. M.
' g 1 Product V Apparent specific gravity 0.0976
Sieve test:- a I l Per cent On 30 mesh 58.7 On 40 mBSIL 23.6 On 60 mesh 14.6 On mesh ..L-' 2.2 On mesh q 0.7 Through 100 mesh 0.2
. EXAMPLE IV Operating conditions Feed stock 40% suspension of Detergent Mix C. Temperature of feed stock. 90' C.
The products of the foregoing examples were all free-flowing, dry powders which retained their free-flowing character after exposure for six days to atmospheres having humidities of 60%, 85% and 93%. The percentage moisture absorbed in such humidity tests are exemplified in the results reported for the products of Example 2. The test is performed as follows:. Definite weighed portions of the detergent under test were placed in open containers which in turn were placed in jars containing saturated aqueous solutions of appropriate inorganic salts in contact with an excess of the solid phase chosen so as to produce 60%, 85% and 93% relative humidities. The jars containing the detergent were then tightly closed and allowed to stand for six days, at the end of which time they were opened and the condition of the detergent noted as to increase in Weight and whether or not it had caked or remained free-flowing. The character of the product is of greater significance than the percentage moisture absorbed since other materials which have absorbed the same amount of moisture may be entirely Wetted and caked.
The sieve test used is similar to that of the A. S. T. M. and represents the relative content and varying size of the different particles of the composition. For comparison with the tests of the foregoing examples, the screen tests of several commercial detergent compositions obtained in the market were as follows:
u 1 l. 11 "Super "Super Suds Dre; Suds" Concentrated" Per cent Per cent Per cent Per cent On 40 mesh 0.8 72. 4 70. 8 67.1
OnBOmesh 17.6 15.1 19.7 22.7 On 100 mesh... 54.4 7.8 7.5 7.8 On 150 mcsh. 14.0 3.1 1.2 1.6 On 200mcsh. 4.8 0.8 0.4 0.4 Through 200 mesh 4.8 0.8 0.4 0.4 Loss 3. 6
grams of water occupies a volume of 25.1- cc. at 30 C. The volume of 25 grams of water at 30 C. divided by the volume of the same weight of the detergent powder at 30 C. gives the apparent specific gravity of the detergent powder. Preferably the compositions for use according to this invention are such as contain 40% active alkylated aromatic hydrocarbon sulfonate. Such compositions are, for example, represented by Detergent Mix C or by the following compositions, which can be spray-dried according to the method disclosed herein. All proportions stated are in parts by weight of anhydrous materials.
EXAMPLE V l Parts Sodium sulfate 36 Sodiumcarbonate 24 Alkylated aromatic hydrocarbon sulfonate 40 Magnesium sulfate; 2
\ EXAMPLE VI Parts Dodecyl benzene sodium sulfonate 40 I Sodium sulfate"; 58.5 Magnesium sulfate"; 0.5 Diethylene glycol 0.5
EXAMPLE VII Parts Dodecyl benzene sodium sulfonate 40 Sodium sulfate 38.5 Sodium carbonate 20 Magnesium sulfate 0.5 Diethylene glycol 0.5
The diethylene glycol which is present in the compositions of Examples VI and VII is used to prevent dusting of any fine particles originally formed as a result of imperfect control of particle size in'the spray-drying operation. It may be replaced by glycerol or similar material to entirely omitted.
Examples VI and VII which contain a smaller added proportion of magnesium sulfate than other disclosed products are particularly suitable for preparations made by dissolving or homogeneously suspending the materials in water containing some original hardness. The hardness of the water, representing magnesium and other metal salts, will be found in the final spray-dried product. When the water used for this purpose is soft or distilled water a greater proportion of magnesium sulfate will be required to com-u.
pensate for the magnesium salts that are absent from the water. Generally from about 0.5 to
1.0% magnesium sulfate (anhydrous basis) is desired in the final spray-dried product.
By operating according to the present invention a substantially uniform non-cakingfreeflowing, particulate detergent composition can be obtained, which is not the case when the watersoluble salt of the aromatic hydrocarbon sulionic acid is dried in a mass and mechanically mixed with sodium sulfate or when a solution of the aromatic hydrocarbon sulfonic acid salt and sodium sulfate in indiscriminate proportions is dried in a mass and then disintegrated mechanically by grinding. Uniformity of'particle size cannot be controlled mechanically nor can the caking characteristics be controlled by purely empirical methods. as is evident from the foregoing description.
It is to be understoodthat the invention is not to be limited by the specific examples hereinabove set forth as they are to be understood as illustrative only. The invention is limited solely oy the following claims.
We claim:
1. A non-caking, free-fiowing particulate solid detergent composition having an apparent specific gravity of about 0.05 to 0.25 and a moisture content of about 1.0 to 5.0% obtained by spraydrying an aqueous solution or homogeneous aqueous suspension, the solid constituents of which comprise a mixture of 35 to 65 parts by weight ofsodiuin sulfate and 65 to 35 parts by weight of a water-soluble salt of a monoalkyl-substituted aromatic hydrocarbon sulfonic acid selected from the group consisting of water-soluble salts of monoalkyl-substituted benzene, toluene and xylene sulfonic acids, the substituted alkyl groups of which contain at least 11 and less than 16 1.,
carbon atoms, to each 100 parts by weight of the solid constituents.
2. A non-caking, free-flowing particulate solid detergent composition of which substantially all the individual particles thereof are retained on an Bil-mesh sieve and which has an apparent 16 carbon atoms, to each 100 parts by weight of the solid constituents.
3. A non-caking, free-flowing particulate solid detergent composition having an apparent specific gravity of about 0.05 to 0.25 and a moisture content of about 1.0 to 5.0% obtained by spray- ,drying an aqueous solution or homogeneous aqueous suspension, the solid constituents of which comprise a mixture of 35 to 65 parts by weight of sodium sulfate and 65 to 35 parts by weight of an alkali-metal salt of a monOalkylated benzene sulfonic acid, the alkyl group oi? which contains at least 11 and less than 16 carbon atoms, to each 100 parts by weight of the solid constituents.
4. A non-calcing, free-flowing particulate solid detergent composition having an apparent specific gravity of about 0.05 to 0.25 and a moisture content of about 1.0 to 5.0% obtained by spraydrying an aqueous solution or homogeneous aqueous suspension, the solid constituents of which comprise a mixture of 35 to 65 parts by weight of sodium sulfate and'65 to 35 parts by i weight of a sodium salt of a monoallclated benzene sulfonic acid, the alkyl group of which contains at least 11 and less than 16 carbon atoms,
to each 100 parts by weight of the solid constituents.
5. A non-caking, free-flowing particulate solid alkylated benzene sulfonic acids, the alkyl groups of which contain at least 11 and less than 16 carbon atoms, to each 100 parts by weight of the solid constituents.
6. A non-caking, free-flowing articulate solid detergent composition having an apparent specific gravity of about 0.05 to 0.25 and a moisture content of about 1.0 to 5.0% obtained by spraydrying an aqueous solution or homogeneous 19 aqueous suspension, the solid constituents of which comprise the following substances in approximately the following proportions by weight: 60 parts of sodium sulfate and 40 parts of sodium salts of a mixture of monoalkylated benzene sulfonic acids, the alkylgroups of which contain at least 11 and less than 16 carbon atoms, to each 100 parts of the solid constituents.
7. A non-caking, free fiowing particulate solid detergent composition having an apparent specontent of about 1.0 to 5.0% obtained by spraycific grayity of about 0.05 to 0.25 and a moisture drying an aqueous solution or homogeneous aqueous suspension, the solid constituents of whichcomprise the following substances in approximately the following proportions by weight: 36 parts of sodium sulfate, 24 partfof sodium carbonate and 40 parts of sodium salts of a mixture of monoalkylated benzene suifonic acids, the alkyl groups of which contain at least 11 and less than 16 carbon atoms, to each 100 parts of the solid constituents.
8. A non-casing, free-flowing particulate solid ent composition having an apparent spe- .1
cific gravity of about 0.05 to 0.25 and a moisture content of about 1.0 to 5.0% obtained by spraydrying an aqueous solution or homogeneous aqueous suspension, the solid constituents of which comprise the following substances in approximately the iollowing proportions by weight: 58.5 parts of sodium sulfate, 40 parts of dodecylbenzene sodium sulfonate and 0.5 part of magnesium sulfate (anhydrous basis), to each 99 parts of the solid constituents.
9. A non-calling, free-flowing particulate solid 43 detergent composition having an apparent specific gravity of about 0.05 to 0.25 and a moisture content of about 1.0 to 5.0% obtained by spraydrying an aqueous solution or homogeneous aqueous suspension, the solid constituents 01 which comprise the following substances in ap proximately the following proportions by weight: 58.5 parts of sodium sulfate, 40 parts of dodecylbenzene sodium sulfonate and 0.5 part of diethylene glycol, to each 99 parts of the solid constituents.
I 10. A non-caking, free-flowing particulate solid I "detergent composition having an apparent SD61.
""" ifie gravity of about 0.05 to 0.25 and a moisture -58.5 parts'of sodium sulfate, 40 parts of dodecylbenzene sodium suli'onate, 0.5 part of magnesium sulfate (anhydrous basis) and 05 part 01' diethylene glycol, to each 99.5 parts of the solid constituents.
mcnorns N. 'r. SAMARAS.
JAY C. HARRIS.
CERTIFICATE OF CORRECTION. v Patent No. 2,298,650. October 15, 191g.
NICHOLAS N 1. SAHARAS, ET AL,
It is hereby certified,that error appears in the printed specification of the above numbered patent requiring correction as follows: Page 3, first column, line 14.2, for "homogenous' reed' homogeneousqline 56, for dedecyl"' read 'dodecy1-; and that the said Letters Patent should be read with this correction therein that the same may conform to the record of the case in the Patent Office.
Signed and sealed this 2).|.th day of November, A. D. lQ+2.'
Henry Van Arsdale,
(Seal) .A'cting Commissioner of Patents.
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US336716A US2298650A (en) | 1938-01-05 | 1940-05-23 | Particulate detergent composition |
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US523479XA | 1938-01-05 | 1938-01-05 | |
US336716A US2298650A (en) | 1938-01-05 | 1940-05-23 | Particulate detergent composition |
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Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
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US2456437A (en) * | 1943-11-24 | 1948-12-14 | Colgate Palmolive Peet Co | Nondusting soap composition and method for making same |
US2465346A (en) * | 1943-07-15 | 1949-03-29 | Lever Brothers Ltd | Dedusting process and product thereof |
US2489955A (en) * | 1943-08-25 | 1949-11-29 | Colgate Palmolive Peet Co | Preparation of nondusting organic detergent compositions |
US2515577A (en) * | 1950-07-18 | Noncaking alkaryl sulfonate | ||
US2526684A (en) * | 1944-07-26 | 1950-10-24 | Monsanto Chemicals | Runproof stocking |
US2592535A (en) * | 1941-08-01 | 1952-04-15 | Lever Brothers Ltd | Process of dedusting soap and the resulting product |
US2619469A (en) * | 1949-12-05 | 1952-11-25 | Colgate Palmolive Peet Co | Synthetic detergent milled flakes |
US2653913A (en) * | 1950-01-21 | 1953-09-29 | Shell Dev | Synthetic detergent cakes |
US2719785A (en) * | 1952-06-02 | 1955-10-04 | California Research Corp | Herbicidal compositions |
US2768095A (en) * | 1952-05-30 | 1956-10-23 | Shell Dev | Process of coating finely divided solid material |
DE1168589B (en) * | 1956-07-27 | 1964-04-23 | Dalli Werke Maeurer & Wirtz | Abrasives for cleaning purposes |
US3446743A (en) * | 1965-04-01 | 1969-05-27 | Chevron Res | Straight-chain alkyl aryl sulfonate detergent compositions |
US3986979A (en) * | 1969-05-15 | 1976-10-19 | Westvaco Corporation | Process for making combination wetting-dispersing agent |
US4040989A (en) * | 1973-05-25 | 1977-08-09 | Colgate-Palmolive Company | Liquid detergent |
EP1914297A1 (en) * | 2006-10-16 | 2008-04-23 | The Procter & Gamble Company | A spray-drying process for preparing a low density, low builder, highly water-soluble spray-dried detergent powder |
WO2013160093A1 (en) * | 2012-04-27 | 2013-10-31 | Unilever N.V. | Process for the production of a detergent granule, detergent granule and detergent composition comprising said granule |
WO2015018620A1 (en) * | 2013-08-09 | 2015-02-12 | Unilever N.V. | Process for the production of a detergent granule, detergent granule and detergent composition comprising said granule |
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1940
- 1940-05-23 US US336716A patent/US2298650A/en not_active Expired - Lifetime
Cited By (21)
Publication number | Priority date | Publication date | Assignee | Title |
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US2515577A (en) * | 1950-07-18 | Noncaking alkaryl sulfonate | ||
US2592535A (en) * | 1941-08-01 | 1952-04-15 | Lever Brothers Ltd | Process of dedusting soap and the resulting product |
US2465346A (en) * | 1943-07-15 | 1949-03-29 | Lever Brothers Ltd | Dedusting process and product thereof |
US2489955A (en) * | 1943-08-25 | 1949-11-29 | Colgate Palmolive Peet Co | Preparation of nondusting organic detergent compositions |
US2456437A (en) * | 1943-11-24 | 1948-12-14 | Colgate Palmolive Peet Co | Nondusting soap composition and method for making same |
US2526684A (en) * | 1944-07-26 | 1950-10-24 | Monsanto Chemicals | Runproof stocking |
US2619469A (en) * | 1949-12-05 | 1952-11-25 | Colgate Palmolive Peet Co | Synthetic detergent milled flakes |
US2653913A (en) * | 1950-01-21 | 1953-09-29 | Shell Dev | Synthetic detergent cakes |
US2768095A (en) * | 1952-05-30 | 1956-10-23 | Shell Dev | Process of coating finely divided solid material |
US2719785A (en) * | 1952-06-02 | 1955-10-04 | California Research Corp | Herbicidal compositions |
DE1168589B (en) * | 1956-07-27 | 1964-04-23 | Dalli Werke Maeurer & Wirtz | Abrasives for cleaning purposes |
US3446743A (en) * | 1965-04-01 | 1969-05-27 | Chevron Res | Straight-chain alkyl aryl sulfonate detergent compositions |
US3986979A (en) * | 1969-05-15 | 1976-10-19 | Westvaco Corporation | Process for making combination wetting-dispersing agent |
US4040989A (en) * | 1973-05-25 | 1977-08-09 | Colgate-Palmolive Company | Liquid detergent |
EP1914297A1 (en) * | 2006-10-16 | 2008-04-23 | The Procter & Gamble Company | A spray-drying process for preparing a low density, low builder, highly water-soluble spray-dried detergent powder |
WO2008047301A1 (en) * | 2006-10-16 | 2008-04-24 | The Procter & Gamble Company | A spray-drying process for preparing a low density, low builder, highly water-soluble spray-dried detergent powder |
US20080261854A1 (en) * | 2006-10-16 | 2008-10-23 | Nigel Patrick Somerville Roberts | Spray-drying process for preparing a low density, low builder, highly water-soluble spray-dried detergent powder |
US7947642B2 (en) | 2006-10-16 | 2011-05-24 | The Procter & Gamble Company | Spray-drying process for preparing a low density, low builder, highly water-soluble spray-dried detergent powder |
WO2013160093A1 (en) * | 2012-04-27 | 2013-10-31 | Unilever N.V. | Process for the production of a detergent granule, detergent granule and detergent composition comprising said granule |
WO2015018620A1 (en) * | 2013-08-09 | 2015-02-12 | Unilever N.V. | Process for the production of a detergent granule, detergent granule and detergent composition comprising said granule |
CN105431513A (en) * | 2013-08-09 | 2016-03-23 | 荷兰联合利华有限公司 | Process for the production of a detergent granule, detergent granule and detergent composition comprising said granule |
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