US2382163A - Detergent briquette - Google Patents
Detergent briquette Download PDFInfo
- Publication number
- US2382163A US2382163A US2382163DA US2382163A US 2382163 A US2382163 A US 2382163A US 2382163D A US2382163D A US 2382163DA US 2382163 A US2382163 A US 2382163A
- Authority
- US
- United States
- Prior art keywords
- water
- detergent
- briquette
- briquettes
- proportions
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000003599 detergent Substances 0.000 title description 96
- 239000004484 Briquette Substances 0.000 title description 74
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 114
- 229910001868 water Inorganic materials 0.000 description 114
- NTHWMYGWWRZVTN-UHFFFAOYSA-N Sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 96
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 82
- 239000000203 mixture Substances 0.000 description 70
- 239000004115 Sodium Silicate Substances 0.000 description 68
- 229910052911 sodium silicate Inorganic materials 0.000 description 66
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 60
- 239000001488 sodium phosphate Substances 0.000 description 50
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 48
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 46
- 235000019801 trisodium phosphate Nutrition 0.000 description 46
- 235000017550 sodium carbonate Nutrition 0.000 description 40
- 229910000029 sodium carbonate Inorganic materials 0.000 description 40
- 239000000463 material Substances 0.000 description 38
- 238000000465 moulding Methods 0.000 description 36
- BPQQTUXANYXVAA-UHFFFAOYSA-N silicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 34
- 239000000470 constituent Substances 0.000 description 32
- 239000004094 surface-active agent Substances 0.000 description 32
- FQENQNTWSFEDLI-UHFFFAOYSA-J Tetrasodium pyrophosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 30
- 238000007792 addition Methods 0.000 description 30
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 30
- 235000019353 potassium silicate Nutrition 0.000 description 24
- 235000011121 sodium hydroxide Nutrition 0.000 description 20
- 239000001187 sodium carbonate Substances 0.000 description 18
- 229940001593 sodium carbonate Drugs 0.000 description 18
- 239000000243 solution Substances 0.000 description 16
- FFQBWYTWHOTQFS-UHFFFAOYSA-N dioxido-bis(trioxidosilyloxy)silane Chemical compound [O-][Si]([O-])([O-])O[Si]([O-])([O-])O[Si]([O-])([O-])[O-] FFQBWYTWHOTQFS-UHFFFAOYSA-N 0.000 description 14
- 230000001965 increased Effects 0.000 description 14
- 239000004615 ingredient Substances 0.000 description 14
- XPPKVPWEQAFLFU-UHFFFAOYSA-J Pyrophosphate Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 12
- 235000011180 diphosphates Nutrition 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- 239000012530 fluid Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 238000005406 washing Methods 0.000 description 10
- 239000003513 alkali Substances 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000005755 formation reaction Methods 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 229910052814 silicon oxide Inorganic materials 0.000 description 6
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000000271 synthetic detergent Substances 0.000 description 6
- 239000000080 wetting agent Substances 0.000 description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate dianion Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 4
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 4
- 230000002411 adverse Effects 0.000 description 4
- 230000001276 controlling effect Effects 0.000 description 4
- 230000000875 corresponding Effects 0.000 description 4
- 238000002425 crystallisation Methods 0.000 description 4
- 230000005712 crystallization Effects 0.000 description 4
- NTGONJLAOZZDJO-UHFFFAOYSA-M disodium;hydroxide Chemical compound [OH-].[Na+].[Na+] NTGONJLAOZZDJO-UHFFFAOYSA-M 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 230000001771 impaired Effects 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- 235000019795 sodium metasilicate Nutrition 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- SOBHUZYZLFQYFK-UHFFFAOYSA-K trisodium;hydroxy-[[phosphonatomethyl(phosphonomethyl)amino]methyl]phosphinate Chemical compound [Na+].[Na+].[Na+].OP(O)(=O)CN(CP(O)([O-])=O)CP([O-])([O-])=O SOBHUZYZLFQYFK-UHFFFAOYSA-K 0.000 description 4
- 238000009736 wetting Methods 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- 240000002989 Euphorbia neriifolia Species 0.000 description 2
- 210000004080 Milk Anatomy 0.000 description 2
- 229940076133 SODIUM CARBONATE MONOHYDRATE Drugs 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K [O-]P([O-])([O-])=O Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 238000005352 clarification Methods 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000003750 conditioning Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- 150000004691 decahydrates Chemical class 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000003247 decreasing Effects 0.000 description 2
- 238000004851 dishwashing Methods 0.000 description 2
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 2
- 229910000397 disodium phosphate Inorganic materials 0.000 description 2
- 235000019800 disodium phosphate Nutrition 0.000 description 2
- MQRJBSHKWOFOGF-UHFFFAOYSA-L disodium;carbonate;hydrate Chemical compound O.[Na+].[Na+].[O-]C([O-])=O MQRJBSHKWOFOGF-UHFFFAOYSA-L 0.000 description 2
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 2
- 230000002708 enhancing Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000004677 hydrates Chemical class 0.000 description 2
- 230000036571 hydration Effects 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 238000010297 mechanical methods and process Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000008267 milk Substances 0.000 description 2
- 235000013336 milk Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- -1 previously described Chemical compound 0.000 description 2
- 230000002035 prolonged Effects 0.000 description 2
- 229910052904 quartz Inorganic materials 0.000 description 2
- 238000005204 segregation Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- 229910000162 sodium phosphate Inorganic materials 0.000 description 2
- 235000011008 sodium phosphates Nutrition 0.000 description 2
- 235000019794 sodium silicate Nutrition 0.000 description 2
- 235000019351 sodium silicates Nutrition 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229910052682 stishovite Inorganic materials 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 229910052905 tridymite Inorganic materials 0.000 description 2
- 238000004450 types of analysis Methods 0.000 description 2
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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/08—Silicates
-
- 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
- C11D3/06—Phosphates, including polyphosphates
Definitions
- This invention relates to an improved briquetted detergent compound and includes a novel process whereby the product may with advantage be produced.
- the briquette of my present invention is unique in its combination of detergent characteristics and other physical and chemical properties which make it highly satisfactory for use in modern mechanical washing operations.
- the problem presented involves not merely the production of a material or mixtures of materials having the desired detergent characteristics but also the development of a product which, in ad dition to meeting that requirement, can be economically produced in the desired physical form possessing other essential physical characteristics.
- the detergent be in briquette form; that the briquettes be sufficiently hard and strong to withstand ordinary handling; non-deliquescent so as to withstand storage and the necessary handling and of such structure as will not disintegrate under the conditions of use.
- the control of the rate at which the alkali is dispensed into the washing operation largely depends upon the dissolving. rate of the briquette, it is desirable that the briquette not only have a satisfactory degree of uniformity in its composition but also that it have a uniform solubility rate.
- composition of the cleansing solution be such as to avoid harmfully affecting the material being washed either by attacking the material or by forming deposits or coatings thereon. It is further essential that the composition of the detergent be such as to avoid deleteriously affecting be chemically and physically stable and I the parts of the mechanical washer and the deposition of scale in the various chambers thereof.
- the resulting blocks of detergent material have usually been reduced to a granular or powdered form before use.
- My improved briquettes consist of a dense crystalline aggregate of relatively uniform composition. They are hard'and strong and chemically and physically stable, being capable of withstanding the conditions of shipment and storage essential to ultimate commercial use without material deterioration, disintegration or deliquescence. They do not disintegrate under normal condi- Also, since they can be produced without resort to high temperatures, various desirable addition agents unstable at higher temperatures may be incorporated therein to meet special water conditions or detergent requirements. Accordingly, objectionable precipitations of natural hardness of the water used may be inhibited or greatly reduced and the detergent action of the resulting washing solution materially improved. Further,
- the detergent mixture of which my improved briquettes are composed consists essentially of trisodium phosphate, sodium silicate, sodium carbonate and water.
- it may also contain tetrasodlum pyrophosphate or a surface
- tetrasodium pyrophosphate is desirable .because of its water conditioning properties but also I have found the use of controlled proportions of this pyrophosphate in my briquettes to improve their physical structure.
- the proportions of the several constituents may be varied over a considerable range, hereinafter. specified, to meet specific detergent requirements without loss of the desirable physical or mechanical characteristios oi the resultant briquette.
- the trisodium phosphate may be introduced in the form of the ordinary commercial hydrated product generally represented by the formula NaaPO4J2I-I2O. Theoretically, this material contains 56.8% water. However, repeated analyses indicate that the water content of the trisodium phosphate which tions of use and have a uniform solubility rate.
- Trisodium phosphate having a higher or lower water content, may be used, providing appropriate compensation be made for the difl'erent proportion of water contained therein.
- materials which react under the process conditions to form tri'sodium phosphate for instance disodium phosphate and caustic soda, may be used.
- the sodium silicate constituent of my briquettes should have an NaaozSioz ratio of not less than 1 nor greater than 2. I have obtained excellent results by supplying the sodium silicate in the form of water glass of 41 B. gravity and consisting of. 8.9% NazO, 28.7% .SiOz and 62.4% water, and reacting the water glass with caustic soda in suflicient proportion to produce a sodium silicate oi the desired NazOtSlO-r ratio. Other water glass or sodium silicate in solid form may be used in accordance with my invention by making appropriate allowance for diflerences in composition.
- sodium metasilicate as such may be substituted wholly or in part for the water glass and caustic soda equivalent.
- substitution is made, due allow ance should also be made for the amount of water which would otherwise be formed by the reaction between the water glass and caustic soda.
- the caustic soda may be supplied in solid form such as the usual commercial grade of about 76% NazO. However, other forms of caustic soda, such as the commercially available 50% solution, may be substituted provided appropriate allowance is made for the difference in composition.
- the sodium carbonate may conveniently be supplied as anhydrous soda ash and the proportions stated in the several formulae appearing herein are based upon the use thereof. However, it may be supplied in the form of hydrates such as mono or deca hydrates, appropriate allowance being made for differences in composition.
- tetrasodium pyrophosphate may be supplied in the usual anhydrous form and proportions thereof appearing herein have reference to such material.
- the compounding of my improved detergent is advantageously carried out in a conventional steam-jacketed kettle equipped with a stirring device.
- I have obtained excellent results in preparing and in duplicating the composition and structure of the briquettes by adhering to the following procedure:
- the predetermined amounts of I water glass, trisodium phosphate, caustic soda and additional water, if any is required, are placed in the kettle and heated with constant agitation until the mass is fluid.
- the temperature is 'then maintained at a maxmum just beyond which substantial evolution of steam would occur with a resultant material loss in water content. Higher temperatures are to be avoided as it is desirable to reduce to a minimum the amount of water lost during the heating operation and to avoid decomposition 01 less stable ingredients.
- the proportion of water in the product may be eflectively controlled by regulation of the total amount of water added tothe batch.
- the maximum temperature to which the material is heated, and at which it is held, depends primarily upon the concentration of the solution in the fluid mass and is usually found to be within the range of about -110 C. The fluid mass is held at this temperature until the mass clarifies,
- the predetermined amount of soda ash is then added and thor oughly mixed with the fluid mass. If the addition of soda ash results in a decrease in temperature to a point at which the mass is too viscous for final pouring, the temperature may be increased until adequate fluidity is obtained, care being taken to avoid temperatures which would result in the material loss of water.
- It tetrasodium pyrophosphate is to be incorporated in the briquettes, it may be added and thoroughly mixed into the mass in the kettle at this point, or it may be found advisable to incorporate the pyrophosphate into the mass prior to the addition of the soda ash, particularly if the pyrophosphate is in a slowly soluble form.
- a so-called surface active agent such material may be introduced into the mixture just prior to withdrawal from the kettle.
- such addition agent is in solid form and has a relatively slow rate of solubility, I prefer to add it prior to the addition of the soda ash.
- Various surface active agents capable of withstanding the necessary processing temperatures in an alkaline environment may be so incorporated in my briquettes to meet special conditions encountered in specific detergent operations for which the briquettes are intended; for example, a product consisting principally of sodium lauryl sulfate, marketed under the trade-name Orvus orone consisting principally of sodium dodecyl benzene sulfonate, marketed under the tradename Nacconol, each of which I have used to advantage.
- the congealed mass cracks and otherwise decrepitates to an extent that prevents removal of the briquette intact from the mold.
- the silicate content should approach its lower limit in order to obtain the most satisfactory conditions with respect to molding time and structure of the briquette.
- anhydrous trisodium phosphate in the finished product is less than about 1% by weight
- the proportion of sodium silicate which can be employed without detrimentally affecting the physical structure of the briquette is limited where less than about 1% by weight of anhydrous trisodium phosphate is present.
- anhydrous sodium silicate in the finished product has found the desirable proportions of anhydrous sodium silicate in the finished product to be within the range of about 1% to about 22% by weight. As the proportion of anhydrous sodium silicate exceeds this maximum, the molding time increases toward an impracticable amount and above an anhydrous silicate content of about 25% briquetting difficulties are encountered. With less than about 1% anhydrous sodium silicate present, the physical characteristics of the briquette are impaired.
- caustic soda in proportions sufllcient to combine with the water glass to form the metasilicate, in which the ratio of Na2O:SiOz is unity, but not in excess of that required to form the orthosilicate in which the ratio of NazOISlOa is 2.
- the proportion of caustic soda so employed is withinthe range required to produce a mixture of metasilicate and orthosilicate in proportions of from 1 to 2 to 2 to 1.
- anhydrous sodium silicate constituent within the range of about 1% to about 22%- whether it be the metasilicate, the orthosilicate or a combination of the two, including a. silicate having a molar NazO:SiO2 ratio of 1%:1 which may be desiging characteristics, and to some extent the structural characteristics, are frequently improved by adjusting the alkalinity of the sodium silicate constituents to approximate that of the sesquisilicate.
- the amount of water present in the detergent composition is of major importance both with respect to molding time and mechanical structure of the resultant briquette and also its detergent content. It is essential that sufficient water be present during the processing to produce under processing conditions a mass sufliciently fluid to permit satisfactory mixing and pouring into the molds and have satisfactory molding characteristics. However, the addition of an excess of water is to be avoided since the processing preferably does not involve conditions under which excess waterwould be eliminated.
- tetrasodium pyrophosphate is to be incorporated in my briquettes, I have found proportions of about by weight usually to be sufficient for most water conditions. However, an amount in excess of 15% may be incorporated, if desirable, without destroying the physical structure of the resultant briquette.
- the proportion of sodium silicate approaches the extreme upper limit, particularly 'when the alkalinity of the silicate approximates l the alkalinity of the silicate constituent approaches that of sodium sesquisiiicate, the proportion of tetrasodium pyrophosphate may be varied throughout the stated range without materially benefiting the physical structure of the resultant briquette.
- the proportion of the soda ash constituent approaches the upper limit of the prescribed range and the proportions of the trisodium phosphate and the sodium silicate constituents are each in the lower portion of their respective ranges, the molding and structural characteristics of the briquette are imp o e y the addition of tetrasodium pyrophosphate.
- a minimum proportion of about 2% to 3% is usually desirable.
- any effective minimum may be used or, if desired, this material may be entirely omitted.
- sodium carbonate is an essential constituent of my briquetted product, the proportions of sodium carbonate present do not appear to be particularly critical.
- the range of variation is usually from about 20% to about 50% by weight but, where the anhydrous sodium silicate content is at the extreme upper end of the range for that ingredient, and tetrasodium pyrophosphate is added in proportions in excess of 15% for improving the molding characteristics, it may be necessary to decrease the soda ash content to an amount even below 20%.
- a maximum of about 5% has been found sufilcient for most purposes where a detergent in briquetted form can advantageously be adopted.
- a proportion as high as 5% is employed, most satisfactory physical structure is obtained where the anhydrous sodium silicate content does not exceed about 15% by weight and the molar ratio of metasilicate to orthosilicate present approximates unity or, in otherwords, the alkalinity approaches'that of the sesquisilicate.
- briquettes of better physical structure are obtained when the sodium silicate constituent consists of the sesquisilicates or a mixture of the meta and ortho silicate.
- Trisodium phosphate ((iodccahydrate) 10 35 10 5 10 5 10 Water glass, 41 B6. 20 20 5 1.5 10 20 Faustic soda 8. 8 8.8 1.4 13. 2 .4 6.4 8. 8 'lctrasodium pyrophosphate. 10 15 10 10 10 10 Soda ash 45. 7 37 29. 6 28. 7 43. 7 44. G 33. 5 Surface active agent. 2. 5 Added water... l5 5 14.2 14 8 1 24.4 24.0 15.2
- the size of the crystal growth appears to be influenced mainly by the sodium silicate content of the melt.
- the crystal size increases with an increase in the percentage of sodium silicate.
- the crystals develop to a size that is visibly evident and, when excessive amounts of sodium silicate are used, the crystals are so large and loosely interlaced that the resulting briquette has impaired mechanical strength. This eifect is more evident where the alkalinity of the silicate approaches that of the orthosilicate.
- a detergent briquette chemically and physically stable, hard, strong and non-deliquescent consisting of a dense crystalline aggregate consisting essentially of the following constituents in proportions by weight within the respective indicated ranges: trisodium phosphate about 1% to 15%, sodium silicate about 1% to 25%, sodium carbonate about 20% to 50%, tetrasodium pyrophosphate about 3% to 25% and water about 30% to 40%, the Na2O:SiOz ratio of the silicate being not less than 1:1 nor greater than 2:1.
- a detergent briquette chemically and physically stable, hard, strong and non-deliquescent consisting of a dense crystalline aggregate consisting essentially of the following constituents in proportions by weight within the respective indicated ranges: trisodium phosphate about 1% to 15%, sodium silicate about 1% to 25%, sodium carbonate about 20% to 50%. tetrasodium pyrophosphate about 3% to 15%, an alkali-stable nonsaponaceous, synthetic, organic, surface active agent 0% to about 5%, and water about 30% to 40% the NazOzsioz ratio of the silicate being not less than 1:1 nor greater than 2:1.
- a detergent briquette chemically and physically stable, hard, strong and non-deliquescent consisting of a dense crystalline aggregate consisting essentially of the following constituents in proportions by weight within the respective indicated ranges: trisodium phosphate about 1% to 15%, sodium v carbonate about 20% to 50% tetrasodium pyrophosphate about 3% to 25%, an amounttoi' an alkali-stable non-saponaceous, synthetic, organic, surface active agent effective substantially to reduce the dissolving rate of the briquette and not exceeding about 5% and water about 30% to 40% silicate about 1% to 25%, sodium,
- a detergent briquette chemically and physically stable, hard, strong and non-deliquescent consisting of a dense crystalline aggregate of approximately the following composition by weight: trisodium phosphate 4.7%, sodium carbonate 37%, tetrasodium pyrophosphate 10%, water 34% and sodium silicate 14.6%, the alkalinity oi the latter approximating that of sodium sesquisilicate.
- a detergent briquette chemically and physically stable, hard, strong and non-deliquescent consisting of a dense crystalline aggregate of approximately the following composition by weight: trisodium phosphate 16.4%; sodium carbonate 29.6%, tetrasodium pyrophosphate 15%, water .0 36%, sodium silicate 2.9 %,the alkalinity of the latter approximating that or sodium metasilicate.
- Trisodium phosphate 16.4% sodium carbonate 29.6%, tetrasodium pyrophosphate 15%, water .0 36%, sodium silicate 2.9 %,the alkalinity of the latter approximating that or sodium metasilicate.
- JAMES DOUGLAS MACMAHON.
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Description
Patented Aug. 14, 1945 DETERGENT BRIQUETTE James Douglas MaoMahon, Nam Fails, N. Y., assignor to The Mathleson Alkali Works, Inc., New York, N. Y., a corporation of Virginia No Drawing. Application January 31, 1942, Serial No. 429,127
6 Claims.
This invention relates to an improved briquetted detergent compound and includes a novel process whereby the product may with advantage be produced.
The briquette of my present invention is unique in its combination of detergent characteristics and other physical and chemical properties which make it highly satisfactory for use in modern mechanical washing operations.
Modern mechanical methods and apparatus for washing dishes, milk cans and the like, particularly where the operation is continuous or prolonged, have presented the serious problem of maintaining an alkali concentration in the wash tanks between desirable and restricted limits. Commercial experience has shown that this may be accomplished in a dependable and virtually automatic manner by dissolving alkaline briquettes in suitable auxiliary equipment and dispensing the resulting solution into the wash tanks at a predetermined rate. A very considerable amount of research has been carried out in view of developing detergents having chemical and physical characteristics satisfactory for this purpose.
The problem presented involves not merely the production of a material or mixtures of materials having the desired detergent characteristics but also the development of a product which, in ad dition to meeting that requirement, can be economically produced in the desired physical form possessing other essential physical characteristics.
For instance, it is desirable that the detergent be in briquette form; that the briquettes be sufficiently hard and strong to withstand ordinary handling; non-deliquescent so as to withstand storage and the necessary handling and of such structure as will not disintegrate under the conditions of use.
Inasmuch as the control of the rate at which the alkali is dispensed into the washing operation largely depends upon the dissolving. rate of the briquette, it is desirable that the briquette not only have a satisfactory degree of uniformity in its composition but also that it have a uniform solubility rate. I
It is, of course, also essential that the composition of the cleansing solution be such as to avoid harmfully affecting the material being washed either by attacking the material or by forming deposits or coatings thereon. It is further essential that the composition of the detergent be such as to avoid deleteriously affecting be chemically and physically stable and I the parts of the mechanical washer and the deposition of scale in the various chambers thereof.
It has been proposed to produce detergent briquettes for such use by fusing the detergent or detergent mixture and casting the fused material by drawing it off into molds to cool. For ex,- ample, briquettes have been produced by fusing mixtures of trisodium posphate and soda ash. However, the relatively high temperatures required to fuse the detergent or detergent mixtures have been a decided handicap in the production of satisfactory detergent briquettes, as many substances, the presence of which is highly desirable in detergent mixtures, are driven off or decomposed at temperatures below their fusion point or at temperatures necessary for fusing other desirable constituents.
This temperature requirement has not permitted the incorporation in detergent mixtures so produced of many very effective water conditioners and surface active agents such as synthetic detergent and wetting agents. Consequently, the use of such fused detergent briquettes has not been wholly satisfactory. For instance, particularly under adverse water conditions, their use has resulted in the precipitation of natural hardness of the water supply and the tendency to form scale on the inner surfaces of the mechanical washers with which the detergent is used. Rapidity of this scale formation depends upon the degree and nature of the hardness of the water and, in general, increases with the concentration of hardness of the water supply. If not periodically removed, this scale interferes with the normalfunctioning of the equipment. Further, this precipitated hardness interferes to a greater or less extent with the cleansing operation.
The presence of a water conditioner such as tetrasodium pyrophosphate (NsAPzO-z) in the alkaline solution tanks of the mechanical washers has been found to inhibit or greatly retard scale formation. Also, the addition of surface active agents has been found further to enhance the cleansing action and to afford improved rinsing.
However, for the reasons stated above, the lncorporation of these materials in fused anhydrous detergent briquettes has been impractical. Detergents have heretofore been produced in block form by crystallization or solidification of the detergent or detergent mixtures from aqueous solutions; for instance, by the evaporation of water therefrom or by causing a chemical or physical union of the water or a proportion there active agent or both.
the latter figure.
of with the detergent. The resulting blocks of detergent material have usually been reduced to a granular or powdered form before use.
It has also been proposed to use these detergent 1 blocks as such in detergent operations. However,
so far as I am aware, the detergent blocks so the physical limitations and deficiencies commonto previous detergent briquettes are overcome. My improved briquettes consist of a dense crystalline aggregate of relatively uniform composition. They are hard'and strong and chemically and physically stable, being capable of withstanding the conditions of shipment and storage essential to ultimate commercial use without material deterioration, disintegration or deliquescence. They do not disintegrate under normal condi- Also, since they can be produced without resort to high temperatures, various desirable addition agents unstable at higher temperatures may be incorporated therein to meet special water conditions or detergent requirements. Accordingly, objectionable precipitations of natural hardness of the water used may be inhibited or greatly reduced and the detergent action of the resulting washing solution materially improved. Further,
the congealing and hardening time of my briquettes during molding is sufficiently rapid to 1 permit their economical commercial production.
The detergent mixture of which my improved briquettes are composed consists essentially of trisodium phosphate, sodium silicate, sodium carbonate and water. Advantageously, it may also contain tetrasodlum pyrophosphate or a surface The presence of tetrasodium pyrophosphate is desirable .because of its water conditioning properties but also I have found the use of controlled proportions of this pyrophosphate in my briquettes to improve their physical structure. As previously stated, the proportions of the several constituents may be varied over a considerable range, hereinafter. specified, to meet specific detergent requirements without loss of the desirable physical or mechanical characteristios oi the resultant briquette.
In the preparation of my briquettes, the trisodium phosphate may be introduced in the form of the ordinary commercial hydrated product generally represented by the formula NaaPO4J2I-I2O. Theoretically, this material contains 56.8% water. However, repeated analyses indicate that the water content of the trisodium phosphate which tions of use and have a uniform solubility rate.
I have used in the development of my improved briquette is approximately 53%. Consequently, the proportions specified herein are based upon Trisodium phosphate, having a higher or lower water content, may be used, providing appropriate compensation be made for the difl'erent proportion of water contained therein. Also, materials which react under the process conditions to form tri'sodium phosphate, for instance disodium phosphate and caustic soda, may
be substituted for an equivalent proportion of trisodium phosphate, appropriateallowance being made for the water content of such reacting ma terials and water produced by the reaction.
The sodium silicate constituent of my briquettes should have an NaaozSioz ratio of not less than 1 nor greater than 2. I have obtained excellent results by supplying the sodium silicate in the form of water glass of 41 B. gravity and consisting of. 8.9% NazO, 28.7% .SiOz and 62.4% water, and reacting the water glass with caustic soda in suflicient proportion to produce a sodium silicate oi the desired NazOtSlO-r ratio. Other water glass or sodium silicate in solid form may be used in accordance with my invention by making appropriate allowance for diflerences in composition. For example, instead of the use of water glass and suflicient caustic soda to react therewith to form the metasilicate, sodium metasilicate as such may be substituted wholly or in part for the water glass and caustic soda equivalent. When such substitution is made, due allow ance should also be made for the amount of water which would otherwise be formed by the reaction between the water glass and caustic soda.
The caustic soda may be supplied in solid form such as the usual commercial grade of about 76% NazO. However, other forms of caustic soda, such as the commercially available 50% solution, may be substituted provided appropriate allowance is made for the difference in composition.
The sodium carbonate may conveniently be supplied as anhydrous soda ash and the proportions stated in the several formulae appearing herein are based upon the use thereof. However, it may be supplied in the form of hydrates such as mono or deca hydrates, appropriate allowance being made for differences in composition.
Similarly, the tetrasodium pyrophosphate may be supplied in the usual anhydrous form and proportions thereof appearing herein have reference to such material.
Before defining the range of proportions of the various ingredients incorporated in my improved briquettes, I shall describe my novel process of compounding and preparing the same.
The compounding of my improved detergent is advantageously carried out in a conventional steam-jacketed kettle equipped with a stirring device. I have obtained excellent results in preparing and in duplicating the composition and structure of the briquettes by adhering to the following procedure: The predetermined amounts of I water glass, trisodium phosphate, caustic soda and additional water, if any is required, are placed in the kettle and heated with constant agitation until the mass is fluid. The temperature is 'then maintained at a maxmum just beyond which substantial evolution of steam would occur with a resultant material loss in water content. Higher temperatures are to be avoided as it is desirable to reduce to a minimum the amount of water lost during the heating operation and to avoid decomposition 01 less stable ingredients. By minimizing the water loss the proportion of water in the product may be eflectively controlled by regulation of the total amount of water added tothe batch. The maximum temperature to which the material is heated, and at which it is held, depends primarily upon the concentration of the solution in the fluid mass and is usually found to be within the range of about -110 C. The fluid mass is held at this temperature until the mass clarifies,
advantageously until maximum clarity is ob-' tained. This usually requires from 10 to 20 minutes, depending upon the compo sition and amount of solute.
After clarification of the mass the predetermined amount of soda ash is then added and thor oughly mixed with the fluid mass. If the addition of soda ash results in a decrease in temperature to a point at which the mass is too viscous for final pouring, the temperature may be increased until adequate fluidity is obtained, care being taken to avoid temperatures which would result in the material loss of water. It tetrasodium pyrophosphate is to be incorporated in the briquettes, it may be added and thoroughly mixed into the mass in the kettle at this point, or it may be found advisable to incorporate the pyrophosphate into the mass prior to the addition of the soda ash, particularly if the pyrophosphate is in a slowly soluble form.
The mixture is then drawn oil? into suitable molds and allowed to congeal until the briquettes have developed sufficient mechanical strength to permit their removal from the mold. The neces- One of the advantages of my invention is that I such surface active agents may be incorporated sary molding time will generally vary from about 1 hour to several hours, depending upon the composition of the mixture. Where a sodium silicate other than water glass is used, it should be placed in the kettle at that stage of the operation where the water glass would have been introduced.
On cooling, detergent compositions of this type seem to expand somewhat and this, combined with their tendency to adhere to metal surfaces of the molds, has previously presented considerable difficulty in the molding of detergent materials. I have found that, by using flexible briquette molds, such as molds made of rubber or similar materials,
I these difllculties are eliminated.
Where it. is desirable to incorporate in the b'riquettes a so-called surface active agent, such material may be introduced into the mixture just prior to withdrawal from the kettle. However, where such addition agent is in solid form and has a relatively slow rate of solubility, I prefer to add it prior to the addition of the soda ash. Various surface active agents capable of withstanding the necessary processing temperatures in an alkaline environment may be so incorporated in my briquettes to meet special conditions encountered in specific detergent operations for which the briquettes are intended; for example, a product consisting principally of sodium lauryl sulfate, marketed under the trade-name Orvus orone consisting principally of sodium dodecyl benzene sulfonate, marketed under the tradename Nacconol, each of which I have used to advantage.
The addition of even a fraction of 1% of many of the so-called surface active agents or synthetic detergent or wetting agents has been found materially to reduce the dissolving rate of the resulting briquette. This effect has been found to increase generally as the amount of the agent is increased. Also, under similar conditions of preparation, the addition of many of these surface active agents somewhat increases the molding time. Though, for some purposes, a reduced dissolving rate is undesirable, the addition of a predetermined amount of a surface active agent is of value in controlling the dissolving rate to meet a Specific requirement in this respect. The primary purpose of the addition of these surface active agents is to increase the wetting power of the washing solution and so tend to improve the detergent and rinsing properties thereof. The addition of many of these materials in proportions as small as 0.1% has a noticeable eflect.
in my briquettes, if desirable, either for controlling the dissolving rate or for increasing the wetting power of the washing solution. However, under many conditions encountered, the detergent mixture need not be so supplemented.
While the proportions of the various ingredients used may be varied over a considerable range without destroying the desirable physical or mechanical properties of the resulting briquette, I have found the permissible range of variation to be rather sharply defined. An increase in the proportion of trisodium phosphate with a corresponding decrease in soda ash, other conditions being the same, tends to decrease the congealing or molding time of the resultant briquette. However, I have found that the proportion of anhydrous trisodium phosphate in the resulting briquette cannot much exceed 15% by weight without detrimentally affecting the structure of the briquette. This is first evidenced by I a tendency for the briquette to develop checks or cracks a day or so after the briquette has been molded. As the trisodium phosphate content is further increased, the congealed mass cracks and otherwise decrepitates to an extent that prevents removal of the briquette intact from the mold. Generally, when the proportion of trisodium phosphate approaches this upper limit of the range for that ingredient, i. e., about 15% by weight, the silicate content should approach its lower limit in order to obtain the most satisfactory conditions with respect to molding time and structure of the briquette.
Where the proportion of anhydrous trisodium phosphate in the finished product is less than about 1% by weight, I have found the briquettes to be so slow in congealing that the molding' time'is excessive. Further, the proportion of sodium silicate which can be employed without detrimentally affecting the physical structure of the briquette is limited where less than about 1% by weight of anhydrous trisodium phosphate is present.
I have found the desirable proportions of anhydrous sodium silicate in the finished product to be within the range of about 1% to about 22% by weight. As the proportion of anhydrous sodium silicate exceeds this maximum, the molding time increases toward an impracticable amount and above an anhydrous silicate content of about 25% briquetting difficulties are encountered. With less than about 1% anhydrous sodium silicate present, the physical characteristics of the briquette are impaired.
Where water glass, such as previously described, or other sodium silicates having a ratio of Nazozsioz less than 1 are used, I add caustic soda in proportions sufllcient to combine with the water glass to form the metasilicate, in which the ratio of Na2O:SiOz is unity, but not in excess of that required to form the orthosilicate in which the ratio of NazOISlOa is 2. In general, best results are obtained where the proportion of caustic soda so employed is withinthe range required to produce a mixture of metasilicate and orthosilicate in proportions of from 1 to 2 to 2 to 1. However, satisfactory results may be obtained with the proportion of anhydrous sodium silicate constituent within the range of about 1% to about 22%- whether it be the metasilicate, the orthosilicate or a combination of the two, including a. silicate having a molar NazO:SiO2 ratio of 1%:1 which may be desiging characteristics, and to some extent the structural characteristics, are frequently improved by adjusting the alkalinity of the sodium silicate constituents to approximate that of the sesquisilicate.
The amount of water present in the detergent composition is of major importance both with respect to molding time and mechanical structure of the resultant briquette and also its detergent content. It is essential that sufficient water be present during the processing to produce under processing conditions a mass sufliciently fluid to permit satisfactory mixing and pouring into the molds and have satisfactory molding characteristics. However, the addition of an excess of water is to be avoided since the processing preferably does not involve conditions under which excess waterwould be eliminated.
I have found the permissible range of proportions of 'water in my briquetted product to be from about 30% to about 40% by weight. It is necessary that the product contain sufficient water to permit satisfactory pouring and molding but an increased amount of water in the product results in a corresponding reduction in the alkali content of the briquette. The proportion of water present also has a distinct effect upon the physical characteristics of the briquette. Generally, proportions of water as high as 40% do not unduly prolong the congealing time or materially impair the physical structure of the briquette. However, proportions of water in excess of about 40% have been found to increase the molding time to impracticability and to affect adversely uniformity of structure of the resulting briquette. When the water content much exceeds this upper limit, there is a tendency toward segregation during the congealing period.
The optimum amount ofwater present in the finished product appears to depend to a considerable extent upon the proportion of other ingredients present. Usually more satisfactory results are obtained where the proportion of water is not much in excess of that required to give sufiicient fluidity for pouring.
In determining the quantity of water, if any, to be added as such in the compounding operation, due consideration must be given to the amount of water present in the various constituents either as water of crystallization or otherwise and of water formed by chemical reactions. A small amount of water may be vaporized or lost during the compounding of the detergent mixture, particularly if the higher temperature be used. The amount of water thus lost is usually of no particular consequence. However, if the amount of water thus lost is excessive, additiona water may be added to the batch.
Where tetrasodium pyrophosphate is to be incorporated in my briquettes, I have found proportions of about by weight usually to be sufficient for most water conditions. However, an amount in excess of 15% may be incorporated, if desirable, without destroying the physical structure of the resultant briquette.
When the proportions of anhydrous trisodium phosphate or of anhydrous sodium silicate are in the upper end of the respective ranges, the molding and structural characteristics of the briquettes are noticeably improved by the addition of tetrasodium pyrophosphate.
When the proportion of sodium silicate approaches the extreme upper limit, particularly 'when the alkalinity of the silicate approximates l the alkalinity of the silicate constituent approaches that of sodium sesquisiiicate, the proportion of tetrasodium pyrophosphate may be varied throughout the stated range without materially benefiting the physical structure of the resultant briquette. Where the proportion of the soda ash constituent approaches the upper limit of the prescribed range and the proportions of the trisodium phosphate and the sodium silicate constituents are each in the lower portion of their respective ranges, the molding and structural characteristics of the briquette are imp o e y the addition of tetrasodium pyrophosphate.
Where the addition of a water conditioner is required, a minimum proportion of about 2% to 3% is usually desirable. However, in accordance with this invention, any effective minimum may be used or, if desired, this material may be entirely omitted.
Though sodium carbonate is an essential constituent of my briquetted product, the proportions of sodium carbonate present do not appear to be particularly critical. The range of variation is usually from about 20% to about 50% by weight but, where the anhydrous sodium silicate content is at the extreme upper end of the range for that ingredient, and tetrasodium pyrophosphate is added in proportions in excess of 15% for improving the molding characteristics, it may be necessary to decrease the soda ash content to an amount even below 20%.
Where the presence of a surface active agent, such as the previously mentioned synthetic detergent and wetting agents, is desirable, a maximum of about 5% has been found sufilcient for most purposes where a detergent in briquetted form can advantageously be adopted. Usually smaller proportions are suflicient. When a proportion as high as 5% is employed, most satisfactory physical structure is obtained where the anhydrous sodium silicate content does not exceed about 15% by weight and the molar ratio of metasilicate to orthosilicate present approximates unity or, in otherwords, the alkalinity approaches'that of the sesquisilicate. E en when smaller proportions of such surface active agents are employed, briquettes of better physical structure are obtained when the sodium silicate constituent consists of the sesquisilicates or a mixture of the meta and ortho silicate.
The following formulae are presented as specific illustrations of proportions of the several constitutents which have been used with advantage in the preparation of my improved briquettes.
It will be understood, however, that my invention is not limited to a product prepared from the particular formulae shown. In each instance the proportions are by weight. For convenient reference to the compositions of the resultant briquette, which subsequently appear, the respective formulae have been consecutively numbered.
Batch No.
Trisodium phosphate ((iodccahydrate) 10 35 10 5 10 Water glass, 41 B6. 20 20 5 1.5 10 20 Faustic soda 8. 8 8.8 1.4 13. 2 .4 6.4 8. 8 'lctrasodium pyrophosphate. 10 15 10 10 10 10 Soda ash 45. 7 37 29. 6 28. 7 43. 7 44. G 33. 5 Surface active agent. 2. 5 Added water... l5 5 14.2 14 8 1 24.4 24.0 15.2
Batch No.
'lrisodium phosphate. 4. 7 4. 7 16.4 4.7 9. 4 2.4 4.7 Sodium silicate l4. 6 14.6 2. 9 22 0.9 3. 8 14.6 Tctrasodiurn pyrophosphate 10 15 10 10 10 10 Soda ash 45. 7 37 29. 6 28. 7 43. 7 44. 6 33. 5 Surface active agent. I 2. 5 Total water (apprnx.). 34 36 35 36. 0 34 35 In the product of the above specific Examples 1, 2, 4 and '7, the alkalinity of the sodium silicate constituent approximated that of the sesquisilicate. In the product of Examples 3.and 5, the alkalinity was that of the metasilicate and in Example 6 the alkalinity was that of the orthosilicate. In the specific Example '7 the particular surface active agent used was that previously referred to as being sold under the tradename florws'fl While my invention is not predicted upon any theory with respect to the reasons for the unique physical characteristics of my improved briquettes, my investigations indicate that their physical structure results, at least in part, from the formation of crystals of mixed salts oi the trisodium phosphate, the carbonate and the silicate with inclusions of greater or less amounts of other constituents present in the mixture. The crystals of mixed salts appear to be definite crystalline substances, though I am not prepared to state with certainty their composition. They appear to have approximately the following composition:
Percent Trisodium phosphateu 6 Sodium carbonate 4 Sodium silicate 40 Water 50 My investigations also indicated that these crystals contain inclusions of sodium carbonate monohydrate. Sodium silicate in various stages of hydration has also been found around the crystalline masses. I
Under some conditions, these crystals grow to considerable size, while under other conditions their presence is hardly visible. The size of the crystal growth appears to be influenced mainly by the sodium silicate content of the melt. In general, the crystal size increases with an increase in the percentage of sodium silicate. At the upper limit of the range of this ingredient, the crystals develop to a size that is visibly evident and, when excessive amounts of sodium silicate are used, the crystals are so large and loosely interlaced that the resulting briquette has impaired mechanical strength. This eifect is more evident where the alkalinity of the silicate approaches that of the orthosilicate.
My observations also appear to indicate that other conditions being the same, an increase in the trisodium phosphate content tends to reduce the size of these crystals. These two opposing influences on crystal growth suggest the possibility of relationship between crystal size and molding time and offer a possible explanation of the improved physical structure of my briquettes. I have observed that the molding time is noticeably increased when the sodium silicate content is near the upper limit of the range where the resulting crystal growth is noticeably, excessive in size and, aspreviously stated, there is a general tendency toward decreased molding time when the trisodium phosphate content is increased which increase I believe tends to decrease the size of the crystals.
Though I have herein described and claimed a process which I have found particularly advantageous in the preparation of my improved briquettes, it will be understood that my invention, with respect to the improved product, is not restricted to a product made by the particular process herein described. Likewise, though I have described my improved briquettes as adapted for use with mechanical washers, it will be understood that they are generally useful where a detergent in briquette form is desirable.
This application is in part a continuation of my co-pending application Serial No. 389,619, filed April 21, 1941. V
I claim:
1. A detergent briquette chemically and physically stable, hard, strong and non-deliquescent consisting of a dense crystalline aggregate consisting essentially of the following constituents in proportions by weight within the respective indicated ranges: trisodium phosphate about 1% to 15%, sodium silicate about 1% to 25%, sodium carbonate about 20% to 50%, tetrasodium pyrophosphate about 3% to 25% and water about 30% to 40%, the Na2O:SiOz ratio of the silicate being not less than 1:1 nor greater than 2:1.
2. A detergent briquette chemically and physically stable, hard, strong and non-deliquescent consisting of a dense crystalline aggregate consisting essentially of the following constituents in proportions by weight within the respective indicated ranges: trisodium phosphate about 1% to 15%, sodium silicate about 1% to 25%, sodium carbonate about 20% to 50%. tetrasodium pyrophosphate about 3% to 15%, an alkali-stable nonsaponaceous, synthetic, organic, surface active agent 0% to about 5%, and water about 30% to 40% the NazOzsioz ratio of the silicate being not less than 1:1 nor greater than 2:1.
3. A detergent briquette chemically and physically stable, hard, strong and non-deliquescent consisting of a dense crystalline aggregate consisting essentially of the following constituents in proportions by weight within the respective indicated ranges: trisodium phosphate about 1% to 15%, sodium v carbonate about 20% to 50% tetrasodium pyrophosphate about 3% to 25%, an amounttoi' an alkali-stable non-saponaceous, synthetic, organic, surface active agent effective substantially to reduce the dissolving rate of the briquette and not exceeding about 5% and water about 30% to 40% silicate about 1% to 25%, sodium,
to sodium carbonate about 20% to 50%, tetrasodium pyrophosphate about 3% to water about to and sodium silicate about 1% to 25%, the alkalinity of the latter approximating that of sodium sesquisilicate.
5. A detergent briquette chemically and physically stable, hard, strong and non-deliquescent consisting of a dense crystalline aggregate of approximately the following composition by weight: trisodium phosphate 4.7%, sodium carbonate 37%, tetrasodium pyrophosphate 10%, water 34% and sodium silicate 14.6%, the alkalinity oi the latter approximating that of sodium sesquisilicate.
6. A detergent briquette chemically and physically stable, hard, strong and non-deliquescent consisting of a dense crystalline aggregate of approximately the following composition by weight: trisodium phosphate 16.4%; sodium carbonate 29.6%, tetrasodium pyrophosphate 15%, water .0 36%, sodium silicate 2.9 %,the alkalinity of the latter approximating that or sodium metasilicate. JAMES; DOUGLAS MACMAHON.
Publications (1)
Publication Number | Publication Date |
---|---|
US2382163A true US2382163A (en) | 1945-08-14 |
Family
ID=3434722
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US2382163D Expired - Lifetime US2382163A (en) | Detergent briquette |
Country Status (1)
Country | Link |
---|---|
US (1) | US2382163A (en) |
Cited By (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4139486A (en) * | 1977-03-22 | 1979-02-13 | The Procter & Gamble Company | Built detergent composition |
US4569780A (en) * | 1978-02-07 | 1986-02-11 | Economics Laboratory, Inc. | Cast detergent-containing article and method of making and using |
US4687121A (en) * | 1986-01-09 | 1987-08-18 | Ecolab Inc. | Solid block chemical dispenser for cleaning systems |
US4690305A (en) * | 1985-11-06 | 1987-09-01 | Ecolab Inc. | Solid block chemical dispenser for cleaning systems |
US4725376A (en) * | 1986-04-23 | 1988-02-16 | Ecolab Inc. | Method of making solid cast alkaline detergent composition |
USRE32763E (en) * | 1978-02-07 | 1988-10-11 | Ecolab Inc. | Cast detergent-containing article and method of making and using |
USRE32818E (en) * | 1978-02-07 | 1989-01-03 | Ecolab Inc. | Cast detergent-containing article and method of using |
US4846989A (en) * | 1988-02-12 | 1989-07-11 | Ecolab Inc. | Solid cast warewashing composition and process for preparing the same |
US4858449A (en) * | 1986-01-09 | 1989-08-22 | Ecolab Inc. | Chemical solution dispenser apparatus and method of using |
US4964185A (en) * | 1986-01-09 | 1990-10-23 | Ecolab Inc. | Chemical solution dispenser apparatus and method of using |
US5137694A (en) * | 1985-05-08 | 1992-08-11 | Ecolab Inc. | Industrial solid detergent dispenser and cleaning system |
US5209864A (en) * | 1991-07-03 | 1993-05-11 | Winbro Group, Ltd. | Cake-like detergent and method of manufacture |
US5318713A (en) * | 1992-06-08 | 1994-06-07 | Binter Randolph K | Solid detergent composition with multi-chambered container |
US5399297A (en) * | 1990-12-03 | 1995-03-21 | Henkel Kommanditgesellschaft Auf Aktien | Solid detergents |
US5505915A (en) * | 1993-10-05 | 1996-04-09 | Ecolab Inc. | Solid chemical dispenser with movable nozzle |
US5719111A (en) * | 1995-02-17 | 1998-02-17 | Lever Brothers Company, Division Of Conopco, Inc. | Process for preparing a solid detergent block |
US5759977A (en) * | 1995-11-13 | 1998-06-02 | Diversey Lever, Inc. | Solid detergent block |
US6060444A (en) * | 1993-12-30 | 2000-05-09 | Ecolab Inc. | Method of making non-caustic solid cleaning compositions |
US6164296A (en) * | 1993-12-30 | 2000-12-26 | Ecolab Inc. | Method of removing waxy/fatty soils from ware with a combination of a nonionic silicone surfactant and a nonionic surfactant |
US6369021B1 (en) | 1999-05-07 | 2002-04-09 | Ecolab Inc. | Detergent composition and method for removing soil |
US6673765B1 (en) | 1995-05-15 | 2004-01-06 | Ecolab Inc. | Method of making non-caustic solid cleaning compositions |
-
0
- US US2382163D patent/US2382163A/en not_active Expired - Lifetime
Cited By (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4139486A (en) * | 1977-03-22 | 1979-02-13 | The Procter & Gamble Company | Built detergent composition |
USRE32763E (en) * | 1978-02-07 | 1988-10-11 | Ecolab Inc. | Cast detergent-containing article and method of making and using |
US4569780A (en) * | 1978-02-07 | 1986-02-11 | Economics Laboratory, Inc. | Cast detergent-containing article and method of making and using |
USRE32818E (en) * | 1978-02-07 | 1989-01-03 | Ecolab Inc. | Cast detergent-containing article and method of using |
US5137694A (en) * | 1985-05-08 | 1992-08-11 | Ecolab Inc. | Industrial solid detergent dispenser and cleaning system |
US4690305A (en) * | 1985-11-06 | 1987-09-01 | Ecolab Inc. | Solid block chemical dispenser for cleaning systems |
US4858449A (en) * | 1986-01-09 | 1989-08-22 | Ecolab Inc. | Chemical solution dispenser apparatus and method of using |
US4964185A (en) * | 1986-01-09 | 1990-10-23 | Ecolab Inc. | Chemical solution dispenser apparatus and method of using |
US4687121A (en) * | 1986-01-09 | 1987-08-18 | Ecolab Inc. | Solid block chemical dispenser for cleaning systems |
US4725376A (en) * | 1986-04-23 | 1988-02-16 | Ecolab Inc. | Method of making solid cast alkaline detergent composition |
US4846989A (en) * | 1988-02-12 | 1989-07-11 | Ecolab Inc. | Solid cast warewashing composition and process for preparing the same |
US5399297A (en) * | 1990-12-03 | 1995-03-21 | Henkel Kommanditgesellschaft Auf Aktien | Solid detergents |
US5209864A (en) * | 1991-07-03 | 1993-05-11 | Winbro Group, Ltd. | Cake-like detergent and method of manufacture |
US5318713A (en) * | 1992-06-08 | 1994-06-07 | Binter Randolph K | Solid detergent composition with multi-chambered container |
US5505915A (en) * | 1993-10-05 | 1996-04-09 | Ecolab Inc. | Solid chemical dispenser with movable nozzle |
US6767884B2 (en) | 1993-12-30 | 2004-07-27 | Ecolab Inc. | Combination of a nonionic silicone surfactant and a nonionic surfactant in a solid block detergent |
US7199095B2 (en) | 1993-12-30 | 2007-04-03 | Ecolab Inc. | Combination of a nonionic silicone surfactant and a nonionic surfactant in a solid block detergent |
US6060444A (en) * | 1993-12-30 | 2000-05-09 | Ecolab Inc. | Method of making non-caustic solid cleaning compositions |
US6164296A (en) * | 1993-12-30 | 2000-12-26 | Ecolab Inc. | Method of removing waxy/fatty soils from ware with a combination of a nonionic silicone surfactant and a nonionic surfactant |
US20060040841A1 (en) * | 1993-12-30 | 2006-02-23 | Ecolab Inc. | Combination of a nonionic silicone surfactant and a nonionic surfactant in a solid block detergent |
US6489278B1 (en) | 1993-12-30 | 2002-12-03 | Ecolab Inc. | Combination of a nonionic silicone surfactant and a nonionic surfactant in a solid block detergent |
US6956019B2 (en) | 1993-12-30 | 2005-10-18 | Ecolab Inc. | Combination of a nonionic silicone surfactant and a nonionic surfactant in a solid block detergent |
US6664219B1 (en) | 1993-12-30 | 2003-12-16 | Ecolab Inc. | Combination of a nonionic silicone surfactant and a nonionic surfactant in a solid block detergent |
US20040254090A1 (en) * | 1993-12-30 | 2004-12-16 | Ecolab Inc. | Combination of a nonionic silicone surfactant and a nonionic surfactant in a solid block detergent |
US5719111A (en) * | 1995-02-17 | 1998-02-17 | Lever Brothers Company, Division Of Conopco, Inc. | Process for preparing a solid detergent block |
US6673765B1 (en) | 1995-05-15 | 2004-01-06 | Ecolab Inc. | Method of making non-caustic solid cleaning compositions |
US5759977A (en) * | 1995-11-13 | 1998-06-02 | Diversey Lever, Inc. | Solid detergent block |
US6812202B2 (en) | 1999-05-07 | 2004-11-02 | Ecolab Inc. | Detergent composition and method for removing soil |
US20040077516A1 (en) * | 1999-05-07 | 2004-04-22 | Ecolab Inc. | Detergent composition and method for removing soil |
US6649586B2 (en) | 1999-05-07 | 2003-11-18 | Ecolab Inc. | Detergent composition and method for removing soil |
US6369021B1 (en) | 1999-05-07 | 2002-04-09 | Ecolab Inc. | Detergent composition and method for removing soil |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2412819A (en) | Detergent briquette | |
US2382163A (en) | Detergent briquette | |
US2382165A (en) | Detergent briquette | |
US2382164A (en) | Detergent briquette | |
US5665694A (en) | Block detergent containing nitrilotriacetic acid | |
JPH041800B2 (en) | ||
CA1148437A (en) | Method for retarding gelation of bicarbonate-carbonate-silicate crutcher slurries | |
US4690770A (en) | Block-form detergent free from alkali hydroxides for use in dishwashing machines and a process for its production | |
US3441511A (en) | Alkali metal hydroxide-containing agglomerates | |
US4294718A (en) | Non-gelling inorganic salt crutcher slurries | |
US2374100A (en) | Water treatment | |
US4869844A (en) | High solids liquid alkaline cleaners | |
US2333443A (en) | Method of preparing detergent | |
US5064554A (en) | Process for the production of detergents in the form of fused blocks containing alkali hydroxides and, optionally, active chlorine for use in dishwashing machines | |
US5419850A (en) | Block detergent containing nitrilotriacetic acid | |
US2282018A (en) | Manufacture of alkali metal silicate detergents | |
US4228025A (en) | Agglomeration process for making granular detergents | |
GB1119380A (en) | Process for preparing a crystalline uniformly sized granular detergent composition | |
US2435453A (en) | Detergent briquette | |
US3285859A (en) | Alkali metal silicates and method for producing the same | |
US3271317A (en) | Silicated sodium hydroxide | |
US3764356A (en) | Hydrated alkali metal silicate glass particles with sequestering agents | |
US2444837A (en) | Detergent briquette | |
US2153872A (en) | Method of making alkali metal silicates | |
EP0804538A1 (en) | Block detergent containing nitrilotriacetic acid |