US2473822A - Method of making same - Google Patents
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- US2473822A US2473822A US2473822DA US2473822A US 2473822 A US2473822 A US 2473822A US 2473822D A US2473822D A US 2473822DA US 2473822 A US2473822 A US 2473822A
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- Prior art keywords
- alkali metal
- sodium
- metasilicate
- polyphosphate
- coated
- Prior art date
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- 238000004519 manufacturing process Methods 0.000 title description 6
- 229910052783 alkali metal Inorganic materials 0.000 description 88
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 80
- 239000000203 mixture Substances 0.000 description 76
- 229920000388 Polyphosphate Polymers 0.000 description 74
- 239000001205 polyphosphate Substances 0.000 description 74
- 235000011176 polyphosphates Nutrition 0.000 description 74
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 68
- 150000001340 alkali metals Chemical class 0.000 description 66
- 239000000463 material Substances 0.000 description 66
- 235000021317 phosphate Nutrition 0.000 description 52
- 239000003599 detergent Substances 0.000 description 50
- NBIIXXVUZAFLBC-UHFFFAOYSA-K [O-]P([O-])([O-])=O Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 38
- 239000010452 phosphate Substances 0.000 description 38
- 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 32
- 238000002156 mixing Methods 0.000 description 32
- 229910000029 sodium carbonate Inorganic materials 0.000 description 32
- 235000017550 sodium carbonate Nutrition 0.000 description 32
- 239000004115 Sodium Silicate Substances 0.000 description 26
- NTHWMYGWWRZVTN-UHFFFAOYSA-N Sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 26
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 26
- 235000019795 sodium metasilicate Nutrition 0.000 description 26
- 229910052911 sodium silicate Inorganic materials 0.000 description 26
- 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 22
- -1 alkali metal metasilicate Chemical class 0.000 description 22
- 239000001187 sodium carbonate Substances 0.000 description 22
- 229940001593 sodium carbonate Drugs 0.000 description 22
- 239000011248 coating agent Substances 0.000 description 20
- 238000000576 coating method Methods 0.000 description 20
- 239000000047 product Substances 0.000 description 20
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 20
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 20
- QQGAZMXZCDSRGV-UHFFFAOYSA-A P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+] Chemical compound P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].P(=O)([O-])([O-])[O-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+] QQGAZMXZCDSRGV-UHFFFAOYSA-A 0.000 description 18
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 16
- YDHWWBZFRZWVHO-UHFFFAOYSA-H [oxido-[oxido(phosphonatooxy)phosphoryl]oxyphosphoryl] phosphate Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O YDHWWBZFRZWVHO-UHFFFAOYSA-H 0.000 description 14
- TVHALOSDPLTTSR-UHFFFAOYSA-H hexasodium;[oxido-[oxido(phosphonatooxy)phosphoryl]oxyphosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O TVHALOSDPLTTSR-UHFFFAOYSA-H 0.000 description 14
- 239000002245 particle Substances 0.000 description 14
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 14
- 238000003860 storage Methods 0.000 description 14
- 239000003513 alkali Substances 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 12
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 10
- 150000008041 alkali metal carbonates Chemical class 0.000 description 10
- 239000000377 silicon dioxide Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 8
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 8
- 229910052708 sodium Inorganic materials 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- 239000002253 acid Substances 0.000 description 6
- 238000004806 packaging method and process Methods 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 6
- GCLGEJMYGQKIIW-UHFFFAOYSA-H Sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 4
- 229910000318 alkali metal phosphate Inorganic materials 0.000 description 4
- 235000012970 cakes Nutrition 0.000 description 4
- 235000011180 diphosphates Nutrition 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 239000008233 hard water Substances 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- BPQQTUXANYXVAA-UHFFFAOYSA-N silicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 4
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 4
- 229910052718 tin Inorganic materials 0.000 description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N tin hydride Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- 108020000803 NANP Proteins 0.000 description 2
- XPPKVPWEQAFLFU-UHFFFAOYSA-J Pyrophosphate Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 2
- 229940048084 Pyrophosphate Drugs 0.000 description 2
- 229940076133 SODIUM CARBONATE MONOHYDRATE Drugs 0.000 description 2
- 206010044565 Tremor Diseases 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 235000012241 calcium silicate Nutrition 0.000 description 2
- JYYOBHFYCIDXHH-UHFFFAOYSA-N carbonic acid;hydrate Chemical class O.OC(O)=O JYYOBHFYCIDXHH-UHFFFAOYSA-N 0.000 description 2
- 238000007385 chemical modification Methods 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000005712 crystallization Effects 0.000 description 2
- 235000013365 dairy product Nutrition 0.000 description 2
- 230000002939 deleterious Effects 0.000 description 2
- 229910003460 diamond Inorganic materials 0.000 description 2
- 239000010432 diamond Substances 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
- 230000000694 effects Effects 0.000 description 2
- 244000144992 flock Species 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 235000012243 magnesium silicates Nutrition 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- TWHXWYVOWJCXSI-UHFFFAOYSA-N phosphoric acid;hydrate Chemical class O.OP(O)(O)=O TWHXWYVOWJCXSI-UHFFFAOYSA-N 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000001488 sodium phosphate Substances 0.000 description 2
- 229940048086 sodium pyrophosphate Drugs 0.000 description 2
- 239000008234 soft water Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 2
- 235000019801 trisodium phosphate Nutrition 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
Definitions
- This invention relates to water softenin detergent compositions and to methods for making the same. It more particularly relates to a combination of alkali metal metasilicate and alkali metal polyphosphate having enhanced properties of stability and improved action in either soft or hard water.
- silica deposits films on objects that are washed and scales upon washing equipment. Since the purpose of using polyphosphates is to prevent the formation of films and scales of magnesium and calcium silicates in hard water, the usefulness of the phosphates is substantially defeated by this undesired reaction between the phosphate and silicate prior to its use.
- the present invention provides a simple and inexpensive solution to the problem described above whereby detergent compositions comprising alkali metal phosphates of sufliciently low alkali metal oxide content to act as an acid when combined with metasilicate, such as those polyphosphates having Nazo'Pzos ratios of 3:2 or below, may suitably be compounded with alkali metal metasilicates to form a perfectly stable product which may be stored indefinitely without caking and without the production of free silica.
- detergent compositions comprising alkali metal phosphates of sufliciently low alkali metal oxide content to act as an acid when combined with metasilicate, such as those polyphosphates having Nazo'Pzos ratios of 3:2 or below, may suitably be compounded with alkali metal metasilicates to form a perfectly stable product which may be stored indefinitely without caking and without the production of free silica.
- the invention contemplates a product comprising alkali metal polyphosphate having a NaaO-PzOs ratio of 3:2 or below, the particles of the phosphate having adhered thereto a layer of alkaline material, and the coated phosphate being admixed with a suitable proportion of alkali metal metasilicate.
- the method oi this invention includes wetting such a phosphate with asmall percentage of water admixing the moistened phosphate with a quantity of alkaline material, which is preferably anhydrous or nearly so and of which anhydrous sodium carbonate is an example, whereby the particles are substantially covered and the free water is taken up to give a dry mix, and ther. combining the so coated phosphate with a dex sired quantity of alkali metal metasilicate.
- flakes or granules of a chosen alkali metal polyphosphate having an alkali metal oxide ratio lower thar 3:2, as stated above. are sprayed or otherwise suitably moistened with a small quantity of water,
- quantities of water up to 5% to be useful but amounts of the 011161 of 1 to 2% are usually most satisfactory and are preferred.
- the spraying may take place in any suitable mixing device, it being preferred to employ mixers which will give rapid mixing and prevent caking of the sprayed material.
- the water may suitably be added in any convenient manner but I have found that a combination of a fine spray with substantial agitation produces the optimum effect.
- the particles are suitably coated with a film of moisture.
- a quantity of powdered alkaline material for example light soda ash, sufficient to coat the phosphate particles substantially completely, is then added while continuing the agitation.
- the particles quickly become completely coated with a substantial layer of alkaline material.
- the stirring is preferably not continued in this part of the process for more than a few minutes to avoid a tendency on the part of the alkaline material layer to rub off under continued agitation.
- Products treated in this manner have been found to have a storage life of more than 6 months and even when exposed in open packages in the relatively humid atmosphere of domestic kitchens or of dairy bottle washing establishments and the like, remain perfectly dry and stable and give clear limpid solutions when ultimately dissolved in water for use.
- Combinations of the phosphate here disclosed with metasilicate, lacking the treatment set forth herein, after having been stored for periods as short as l or 2 weeks cake badly and give definite silica flock precipitates when dissolved in water.
- Phosphate flakes which have been treated by the prior art spot-coating technique for a purpose not contemplated by this invention and then combined with a metasilicate are found to store reasonably well in substantially air and moisture tight containers.
- NaePqOn sodium tetraphosphate
- granules are placed in a ribbon mixer and sprayed with .9 lb. of water while mixing. After 2 minutes 12 lbs. of light soda ash (NazCOs), are added and the mixing is continued for 1 to 2 minutes. Then 227 lbs. of sodium metasilicate (NazSiOa), are added and the mixing is continued for 5 minutes.
- NazSiOa sodium metasilicate
- alkali metal polyphosphates generally where the ratio of alkali metal oxide to P105 is 3:2 or below. Included in this classification are alkali metal tetraphosphates, such as sodium tetraphosphate (NauPrOn).
- alkali metal septaphosphates such as sodium septaphosphate (NanP'iOez)
- alkali metal hexametaphosphates such as sodium hexametaphosphate (NaPOslc
- alkali metal hexapolyphosphates such as sodium hexapolyphosphate (NasPsOre)
- alkali metal decaphos phates such as sodium decaphosphate (NanPioOm
- Na20-P2O5 ratios poiyphosphates of other alkali metals are intended to be disclosed.
- any substantially anhydrous alkaline material compatible with the other two ingredients of the mixture and imparting no deleterious qualities to a detergent composition may be employed.
- substantially anhydrous alkaline materials is meant generally those materials within the general disclosure herein whose aflinity for water of crystallization is sufliciently unsatisfied so that they possess a substantial afflnity for further water.
- anhydrous alkali metal pyrophosphates such as sodium pyrophosphate
- anhydrous trialkali phosphates such as trisodium phosphate
- alkali carbonate monohydrates such as sodium carbonate monohydrate, trialkali phosphate monohydrates.
- I may use any alkali metal metasilicate for admixture with the thus coated phosphate.
- the metasilicate may be suitably employed in amounts varying between 50 and of the final detergent product, depending upon the ultimate use to which the detergent mixture is to be applied and the desired alkalinity of such mixture for such use.
- the method of producing stable water softening detergent compositions of alkali metal metasilicates and alkali metal polyphosphates having an alkali content suillciently low to render them acid to alkali metal metasilicates which includes the steps of substantially completely coating said alkali metal polyphosphate with a substantially anhydrous alkaline material chosen from the group of alkali metal carbonates and alkali metal non-polyphosphate phosphates, and combining said coated polyphosphate with alkali metal metasilicate.
- the method 01 producing a stable water softening detergent composition, which includes the steps of moistening sodium tetraphosphate with not more than 5% of water, substantially completely coating said tetraphosphate with between 10% and 25% of sodium carbonate, and combining said coated tetraphosphate with sodium metasilicate.
- the method of producing a stable water softening detergent composition which includes the steps of moistening sodium tetraphosphate with not more than 5% of water, substantially completely coating said moistened tetraphosphate with between 10% and 25% of tetrasodium pyrophosphate, and combining said coated tetraphosphate with sodium metasilicate.
- the method of producing .a stable water softening detergent materal which includes the steps of moistening sodium decaphosphate with not more than 5% of water, substantially completely coating said sodium decaphosphate with between 10% and 25% of sodium carbonate, and combining said coated decaphosphate with sodium metasilicate.
- the method of producing a stable water softening detergent material which includes the steps of moistening sodium decaphosphate with not more than 5% of water. substantially completely coating said sodium decaphosphate with between 10% and 25% of tetrasodium pyrophosphate, and combining said coated decaphosphate with sodium meta-silicate.
- a stable water softening detergent material consisting essentially of a mixture of an alkali metal polyphosphate in which the ratio of alkali metal oxide to phosphorus pentoxide is 3:2 or less, said polyphosphate being coated substantially entirely with a material chosen from the group of alkali metal carbonates and alkali 'rnetal non-polyphosphate phosphates. and alkali metal metasilicate. said polyphosphate and said metasilicate being maintained substantially out of contact with each other in said mixture by said material.
- a stable water softening detergent material consisting essentially of a mixture of an alkali metal polyphosphate in which the ratio of alkali metal oxide to phosphorus pentoxide is 3:2 or less, said polyphosphate being coated substantially entirely with sodium carbonate, and alkali metal metasilicate, said polyphosphate and said metasilicate being maintained substantially out of contact with each other in said mixture by said sodium carbonate.
- a stable water softening detergent material consisting essentially of a mixture of an alkali metal polyphosphate in which the ratio of alkali'metal oxide to phosphorus pentoxide is 3:2 or less, said polyphosphate being coated substantially entirely with tetrasodium pyrophosphate, and alkali metasilicate, said polyphosphate and said metasilicate being maintained substantially out of contact with each other in said mixture by said tetrasodium pyrophosphate.
- a stable water softening detergent composition consisting essentially of sodium tetraphosphate substantially completely coated with an alkaline material chosen from the group of alkali metal carbonates and alkali metal nonpolyphosphate phosphates, and sodium metasllicate, said tetraphosphate and said metasilicate being maintained substantially out of contact with each other in said mixture by said material.
- a stable water softening detergent composition consistingessentially of sodium tetraphosphate substantially completely coated with sodium carbonate. and sodium metasilicate, said tetraphosphate and said metasilicate being maintained substantially out of contact with each other in said mixture by said sodium carbonate.
- a stable water softening detergent composition consisting essentlally of sodium tetraphosphate substantially completely coated with tetrasodium pyrophosphate, and sodium metasilicate, said tetraphosphate and said metasilicate being maintained substantially out of contact with each other in said mixture by said tetrasodium pyrophosphate.
- a stable water softening detergent composition consisting essentially of sodium decaphosphate substantially completely coated with an alkaline material chosen from the group of alkali metal carbonates and alkali metal nonpolyphosphate phosphates, and sodium metasilicate, said decaphosphate and said metasiiicate being maintained substantially out of contact with each other in said mixture by said material.
- a stable water softening detergent composition consisting essentially of sodium decaphosphate substantially completely coated with sodium carbonate, and sodium metasilicate,
- said decaphosphate and said metasilicate being maintained substantially out of contact with each other in said mixture by said sodium carbonate.
- a stable water softening detergent composition consisting essentially of sodium decaphosphate substantially completely coated with tetrasodium pyrophosphate, and sodium metasilicate, said decaphosphate and said metasllicate being maintained substantially out of contact with each other in said mixture by said pyrophosphate.
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- Detergent Compositions (AREA)
Description
Patented June 21, 1949 WATER SOFTENING DETERGENT AND METHOD OF MAKING SAME Edward A. Robinson, Pittsburgh, Pa., assignor to Diamond Alkali Company, Cleveland, Ohio, a
corporation of Delaware Application November 13, 1948, Serial No. 109,439
No Drawing.
21 Claims.
This invention relates to water softenin detergent compositions and to methods for making the same. It more particularly relates to a combination of alkali metal metasilicate and alkali metal polyphosphate having enhanced properties of stability and improved action in either soft or hard water.
The use of combinations of alkali metal metasilicates and alkali metal polyphosphates has heretofore been proposed for various detergent purposes. Insofar as such compositions containing polyphosphates having a higher ratio of NazO to P205 than 3.2 are concerned, such products have been found to be satisfactory both from the standpoint of effectiveness for the purpose intended and stability for periods of normal storage. However, combinations of alkali metal metasilicates and polyphosphates having a NazO-PzOa ratio of 3:2 or below have not been as satisfactory principally because even after relatively short periods of storage, a reaction occurs between the somewhat acid polyphosphate and the alkaline silicate, which reaction results in the release of free silica. As a consequence of this reaction,.such products cake badly in storage. In addition, when such a composition is used as a detergent, the thus formed silica deposits films on objects that are washed and scales upon washing equipment. Since the purpose of using polyphosphates is to prevent the formation of films and scales of magnesium and calcium silicates in hard water, the usefulness of the phosphates is substantially defeated by this undesired reaction between the phosphate and silicate prior to its use.
While I have not observed that the art has attempted to solve this specific problem before, it has been proposed to spot-coat thin flakes of various alkali metal phosphates with alkaline materials in order to render the said prosphates compatible to soap in solution. Whatever may be the usefulness of this expedient, flakes so spotcoated have exposed uncoated surfaces and when such spot-coated materials are mixed with alkali metal metasilicates, the undesired reaction referred to above occurs with consequent caking on storage and cloudy solutions on use.
The present invention provides a simple and inexpensive solution to the problem described above whereby detergent compositions comprising alkali metal phosphates of sufliciently low alkali metal oxide content to act as an acid when combined with metasilicate, such as those polyphosphates having Nazo'Pzos ratios of 3:2 or below, may suitably be compounded with alkali metal metasilicates to form a perfectly stable product which may be stored indefinitely without caking and without the production of free silica.
In general, the invention contemplates a product comprising alkali metal polyphosphate having a NaaO-PzOs ratio of 3:2 or below, the particles of the phosphate having adhered thereto a layer of alkaline material, and the coated phosphate being admixed with a suitable proportion of alkali metal metasilicate. The method oi this invention, in general, includes wetting such a phosphate with asmall percentage of water admixing the moistened phosphate with a quantity of alkaline material, which is preferably anhydrous or nearly so and of which anhydrous sodium carbonate is an example, whereby the particles are substantially covered and the free water is taken up to give a dry mix, and ther. combining the so coated phosphate with a dex sired quantity of alkali metal metasilicate.
In the practice of this invention, flakes or granules of a chosen alkali metal polyphosphate having an alkali metal oxide ratio lower thar 3:2, as stated above. are sprayed or otherwise suitably moistened with a small quantity of water, For this purpose I have found quantities of water up to 5% to be useful but amounts of the 011161 of 1 to 2% are usually most satisfactory and are preferred. The spraying may take place in any suitable mixing device, it being preferred to employ mixers which will give rapid mixing and prevent caking of the sprayed material. The water may suitably be added in any convenient manner but I have found that a combination of a fine spray with substantial agitation produces the optimum effect. After about a minute or so of mixing with the water, the particles are suitably coated with a film of moisture. A quantity of powdered alkaline material, for example light soda ash, sufficient to coat the phosphate particles substantially completely, is then added while continuing the agitation. The particles quickly become completely coated with a substantial layer of alkaline material. The stirring is preferably not continued in this part of the process for more than a few minutes to avoid a tendency on the part of the alkaline material layer to rub off under continued agitation. Ac-
cordingly, after preferably not more than 5 minutes of agitation of the alkaline material coated phosphate, a suitable amount of alkali metal metasilicate is added while continuing agitation. After about 5 minutes more of mixing, the prodnot is dry, free-flowing and granular and ready to be packed into shipping containers.
Products treated in this manner have been found to have a storage life of more than 6 months and even when exposed in open packages in the relatively humid atmosphere of domestic kitchens or of dairy bottle washing establishments and the like, remain perfectly dry and stable and give clear limpid solutions when ultimately dissolved in water for use. Combinations of the phosphate here disclosed with metasilicate, lacking the treatment set forth herein, after having been stored for periods as short as l or 2 weeks cake badly and give definite silica flock precipitates when dissolved in water. Phosphate flakes which have been treated by the prior art spot-coating technique for a purpose not contemplated by this invention and then combined with a metasilicate are found to store reasonably well in substantially air and moisture tight containers. However, immediately upon the package being broken the exposure to the relatively humid air of the normal place of use of such materials results in substantial immediate reaction between the unprotected phosphate and the metasilicate whereby caking occurs particularly in materials not immediately used and subsequent use yields the characteristic silica precipitate in water solutions.
For a further understanding of the invention and further to teach those skilled in the art of the manner in which this invention may be practiced, the following specific examples of its practice are ofiered:
l. 60 lbs. of sodium tetraphosphate (NaePqOn). granules are placed in a ribbon mixer and sprayed with .9 lb. of water while mixing. After 2 minutes 12 lbs. of light soda ash (NazCOs), are added and the mixing is continued for 1 to 2 minutes. Then 227 lbs. of sodium metasilicate (NazSiOa), are added and the mixing is continued for 5 minutes. The resulting product, which is dry, free-flowing, granular, and substantially free from dusty particles. is then ready for packaging and is round to be stable to storage for indefinite periods.
2. 90 lbs. of sodium decaphosphate (NauPloOai) is placed in a ribbon mixer and sprayed with 1.35 lbs. of water while mixing. After 2 minutes 22.5 lbs. of light soda ash are added and the mixing is continued for 1 to 2 minutes.
Then 186 lbs. of sodium metasilicate are added and the mixing is concluded at the end of 5 minutes. The product is comparable to that obtained in the process of that of Example 1 and is found to have indefinite storage life without chemical modification.
3. 24 lbs. of sodium hexametaphosphate (Nail-03M. are placed in a ribbon mixer and sprayed with .35 lb. of water while mixing. After 2 minutes, 6 lbs. of light soda ash are added and the mixing is continued for 1-2 minutes. Then 2'70 lbs. of sodium metasilicate are added and the mixing continued for 5 minutes. The product is then ready. for packaging.
4. 120 lbs. of sodium septaphosphate (NaaPrOzz are placed in a ribbon mixer and sprayed with 1.8 lbs. of water while mixing. After 2 minutes 30 lbs. of powdered anhydrous tetrasodium pyrophosphate are added and the mixing continued for 1 -2 minutes. Then 150 lbs. of sodium metasilicate are added and the mixing is continued for 5 minutes. The product is then ready for packaging.
The present process is applicable to alkali metal polyphosphates generally where the ratio of alkali metal oxide to P105 is 3:2 or below. Included in this classification are alkali metal tetraphosphates, such as sodium tetraphosphate (NauPrOn). alkali metal septaphosphates, such as sodium septaphosphate (NanP'iOez), alkali metal hexametaphosphates, such as sodium hexametaphosphate (NaPOslc, alkali metal hexapolyphosphates, such as sodium hexapolyphosphate (NasPsOre), and alkali metal decaphos phates, such as sodium decaphosphate (NanPioOm Where reference is made herein to Na20-P2O5 ratios, poiyphosphates of other alkali metals are intended to be disclosed. While it has been found preferable to employ anhydrous sodium carbonate suitably in the form of light soda ash as the alkaline material for coating the phosphate particles, any substantially anhydrous alkaline material compatible with the other two ingredients of the mixture and imparting no deleterious qualities to a detergent composition may be employed. By substantially anhydrous alkaline materials is meant generally those materials within the general disclosure herein whose aflinity for water of crystallization is sufliciently unsatisfied so that they possess a substantial afflnity for further water. Examples of materials in addition to that mentioned above which have been found useful in this connection are anhydrous alkali metal pyrophosphates, such as sodium pyrophosphate, anhydrous trialkali phosphates, such as trisodium phosphate, alkali carbonate monohydrates, such as sodium carbonate monohydrate, trialkali phosphate monohydrates. and the like. These materials may be used in quantities varying between about 10 and 25% of the weight of the dry phosphate. In addition, I may use any alkali metal metasilicate for admixture with the thus coated phosphate. The metasilicate may be suitably employed in amounts varying between 50 and of the final detergent product, depending upon the ultimate use to which the detergent mixture is to be applied and the desired alkalinity of such mixture for such use.
While I have described in detail certain forms of my invention and certain specific examples of its practice, I do not wish to be understood as limiting myself to the use of such examples as I realize that changes within the scope of the invention are possible, and I further intend each step in the following claims to refer to all equivalent steps for accomplishing the same result in substantially the same or equivalent manner, it being my purpose to cover my invention broadly in whatever form its principle may be utilized.
What is claimed is:
1. The method of producing stable water softening detergent compositions of alkali metal metasilicate and alkali metal polyphosphate, wherein such polyphosphate has an alkali metal oxide content with relation to P205 of 3:2 or less, which includes the steps of molstening said polyphosphate, substantially completely coating said polyphosphate with a substantially anhydrous alkaline material chosen from the group of alkali metal carbonates and alkali metal non-polyphosphate phosphates, and combining said coated polyphosphate with alkali metal metasilicate.
2. The method of claim 1 wherein the substantially anhydrous alkaline material is sodium carbonate.
3. The method of claim 1 wherein the substantially anhydrous alkaline material is tetrasodium pyrophosphate.
4. The method of producing stable water softening detergent compositions of alkali metal metasilicates and alkali metal polyphosphates having an alkali content suillciently low to render them acid to alkali metal metasilicates, which includes the steps of substantially completely coating said alkali metal polyphosphate with a substantially anhydrous alkaline material chosen from the group of alkali metal carbonates and alkali metal non-polyphosphate phosphates, and combining said coated polyphosphate with alkali metal metasilicate.
5. The method of claim 4 wherein the substantially anhydrous alkaline material is sodium carbonate.
6. The method of claim 4 wherein the substantially anhydrous alkaline material is tetrasodium DYrophosphate.
7. The method of producing a stable water softening detergent composition of alkali metal metasilicate and alkali metal polyphosphate, wherein said phosphate has a ratio of alkali metal oxide to phosphorus pentoxide of 3:2 or less, which includes the steps of moistening said phosphate with less than 5% of water while stirring, substantially completely coating said phosphate with between and 25% of powdered sodium carbonate based on the weight of the dry phosphate, and combining said coated phosphate with alkali metal metasilicate.
8. The method of producing a stable water softening detergent composition of alkali metal metasilicate and alkali metal polyphosphate, wherein said polyphosphate has a ratio of alkali metal oxide to phosphorus pentoxide of 3:2 or less, which includes the steps of moistening said polyphosphate with less than 5% of water while stirring, substantially completely coating said polyphosphate with between 10% and 25% of powdered tetrasodium pyrophosphate based on the weight of the dry polyphosphate. and combining said coated polyphosphate with alkali metal metasilicate.
9. The method 01 producing a stable water softening detergent composition, which includes the steps of moistening sodium tetraphosphate with not more than 5% of water, substantially completely coating said tetraphosphate with between 10% and 25% of sodium carbonate, and combining said coated tetraphosphate with sodium metasilicate.
10. The method of producing a stable water softening detergent composition, which includes the steps of moistening sodium tetraphosphate with not more than 5% of water, substantially completely coating said moistened tetraphosphate with between 10% and 25% of tetrasodium pyrophosphate, and combining said coated tetraphosphate with sodium metasilicate.
11. The method of producing .a stable water softening detergent materal, which includes the steps of moistening sodium decaphosphate with not more than 5% of water, substantially completely coating said sodium decaphosphate with between 10% and 25% of sodium carbonate, and combining said coated decaphosphate with sodium metasilicate.
12. The method of producing a stable water softening detergent material, which includes the steps of moistening sodium decaphosphate with not more than 5% of water. substantially completely coating said sodium decaphosphate with between 10% and 25% of tetrasodium pyrophosphate, and combining said coated decaphosphate with sodium meta-silicate.
13,. A stable water softening detergent material consisting essentially of a mixture of an alkali metal polyphosphate in which the ratio of alkali metal oxide to phosphorus pentoxide is 3:2 or less, said polyphosphate being coated substantially entirely with a material chosen from the group of alkali metal carbonates and alkali 'rnetal non-polyphosphate phosphates. and alkali metal metasilicate. said polyphosphate and said metasilicate being maintained substantially out of contact with each other in said mixture by said material.
14. A stable water softening detergent material consisting essentially of a mixture of an alkali metal polyphosphate in which the ratio of alkali metal oxide to phosphorus pentoxide is 3:2 or less, said polyphosphate being coated substantially entirely with sodium carbonate, and alkali metal metasilicate, said polyphosphate and said metasilicate being maintained substantially out of contact with each other in said mixture by said sodium carbonate.
15. A stable water softening detergent material consisting essentially of a mixture of an alkali metal polyphosphate in which the ratio of alkali'metal oxide to phosphorus pentoxide is 3:2 or less, said polyphosphate being coated substantially entirely with tetrasodium pyrophosphate, and alkali metasilicate, said polyphosphate and said metasilicate being maintained substantially out of contact with each other in said mixture by said tetrasodium pyrophosphate.
16. A stable water softening detergent composition consisting essentially of sodium tetraphosphate substantially completely coated with an alkaline material chosen from the group of alkali metal carbonates and alkali metal nonpolyphosphate phosphates, and sodium metasllicate, said tetraphosphate and said metasilicate being maintained substantially out of contact with each other in said mixture by said material.
17. A stable water softening detergent composition consistingessentially of sodium tetraphosphate substantially completely coated with sodium carbonate. and sodium metasilicate, said tetraphosphate and said metasilicate being maintained substantially out of contact with each other in said mixture by said sodium carbonate.
18. A stable water softening detergent composition consisting essentlally of sodium tetraphosphate substantially completely coated with tetrasodium pyrophosphate, and sodium metasilicate, said tetraphosphate and said metasilicate being maintained substantially out of contact with each other in said mixture by said tetrasodium pyrophosphate.
19. A stable water softening detergent composition consisting essentially of sodium decaphosphate substantially completely coated with an alkaline material chosen from the group of alkali metal carbonates and alkali metal nonpolyphosphate phosphates, and sodium metasilicate, said decaphosphate and said metasiiicate being maintained substantially out of contact with each other in said mixture by said material.
20. A stable water softening detergent composition consisting essentially of sodium decaphosphate substantially completely coated with sodium carbonate, and sodium metasilicate,
said decaphosphate and said metasilicate being maintained substantially out of contact with each other in said mixture by said sodium carbonate.
21. A stable water softening detergent composition consisting essentially of sodium decaphosphate substantially completely coated with tetrasodium pyrophosphate, and sodium metasilicate, said decaphosphate and said metasllicate being maintained substantially out of contact with each other in said mixture by said pyrophosphate.
EDWARD A. ROBINSON.
8 summons 0mm The following references are of record in the tile of this patent:
UNITED STATES PATENTS Number Name Date 1,979,926 Zinn Nov. 6, 1934 08,651 Zinn July 16, 1935 .559 Tremor June 13, 1944 64 MacMahon Aux. 14, 1945 2. 465 MacMahon Aug. 14, 1945 2,396,918. Hubbard et al Mar. 19, 1946
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2473822A true US2473822A (en) | 1949-06-21 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US2473822D Expired - Lifetime US2473822A (en) | Method of making same |
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| Country | Link |
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| US (1) | US2473822A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2712529A (en) * | 1948-10-21 | 1955-07-05 | Procter & Gamble | Detergent composition |
| US2807807A (en) * | 1955-04-11 | 1957-10-01 | Hargivys Inc | Sediment prevention means |
| US2895916A (en) * | 1956-05-15 | 1959-07-21 | Procter & Gamble | Method for preparing detergent compositions |
| US3231561A (en) * | 1962-01-03 | 1966-01-25 | Economics Lab | Fatty acid sugar esters and fatty acid sugar-boron esters |
| US4113644A (en) * | 1975-02-20 | 1978-09-12 | Ashcraft William R | Protected glassy phosphate detergent additive |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1979926A (en) * | 1933-09-05 | 1934-11-06 | Victor Chemical Works | Water softener |
| US2008651A (en) * | 1933-09-05 | 1935-07-16 | Victor Chemical Works | Method of coating flakes |
| US2351559A (en) * | 1944-06-13 | Process for the preparation of | ||
| US2382165A (en) * | 1945-08-14 | Detergent briquette | ||
| US2382164A (en) * | 1945-08-14 | Detergent briquette | ||
| US2396918A (en) * | 1938-11-04 | 1946-03-19 | Monsanto Chemicals | Water-treating composition |
-
0
- US US2473822D patent/US2473822A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2351559A (en) * | 1944-06-13 | Process for the preparation of | ||
| US2382165A (en) * | 1945-08-14 | Detergent briquette | ||
| US2382164A (en) * | 1945-08-14 | Detergent briquette | ||
| US1979926A (en) * | 1933-09-05 | 1934-11-06 | Victor Chemical Works | Water softener |
| US2008651A (en) * | 1933-09-05 | 1935-07-16 | Victor Chemical Works | Method of coating flakes |
| US2396918A (en) * | 1938-11-04 | 1946-03-19 | Monsanto Chemicals | Water-treating composition |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2712529A (en) * | 1948-10-21 | 1955-07-05 | Procter & Gamble | Detergent composition |
| US2807807A (en) * | 1955-04-11 | 1957-10-01 | Hargivys Inc | Sediment prevention means |
| US2895916A (en) * | 1956-05-15 | 1959-07-21 | Procter & Gamble | Method for preparing detergent compositions |
| US3231561A (en) * | 1962-01-03 | 1966-01-25 | Economics Lab | Fatty acid sugar esters and fatty acid sugar-boron esters |
| US4113644A (en) * | 1975-02-20 | 1978-09-12 | Ashcraft William R | Protected glassy phosphate detergent additive |
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