US2986449A - Process for the production of alkali metal polyphosphates - Google Patents
Process for the production of alkali metal polyphosphates Download PDFInfo
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- US2986449A US2986449A US620820A US62082056A US2986449A US 2986449 A US2986449 A US 2986449A US 620820 A US620820 A US 620820A US 62082056 A US62082056 A US 62082056A US 2986449 A US2986449 A US 2986449A
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- alkali metal
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- orthophosphate
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- sodium
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- 229910052783 alkali metal Inorganic materials 0.000 title claims description 84
- 239000001205 polyphosphate Substances 0.000 title claims description 29
- 235000011176 polyphosphates Nutrition 0.000 title claims description 29
- 150000001340 alkali metals Chemical class 0.000 title claims description 24
- 238000000034 method Methods 0.000 title claims description 24
- 238000004519 manufacturing process Methods 0.000 title claims description 17
- 229920000388 Polyphosphate Polymers 0.000 title description 26
- -1 ALKALI METAL SALT Chemical class 0.000 claims description 43
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 16
- 239000011574 phosphorus Substances 0.000 claims description 16
- 229910052698 phosphorus Inorganic materials 0.000 claims description 16
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims description 16
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 claims description 15
- 239000002253 acid Substances 0.000 claims description 14
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 12
- 238000010438 heat treatment Methods 0.000 claims description 8
- 239000000243 solution Substances 0.000 description 26
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- 238000007792 addition Methods 0.000 description 15
- NCPXQVVMIXIKTN-UHFFFAOYSA-N trisodium;phosphite Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])[O-] NCPXQVVMIXIKTN-UHFFFAOYSA-N 0.000 description 12
- 235000019832 sodium triphosphate Nutrition 0.000 description 11
- 239000000203 mixture Substances 0.000 description 9
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 9
- KWSLGOVYXMQPPX-UHFFFAOYSA-N 5-[3-(trifluoromethyl)phenyl]-2h-tetrazole Chemical compound FC(F)(F)C1=CC=CC(C2=NNN=N2)=C1 KWSLGOVYXMQPPX-UHFFFAOYSA-N 0.000 description 8
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 6
- 230000001603 reducing effect Effects 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 229910019142 PO4 Inorganic materials 0.000 description 5
- HWGNBUXHKFFFIH-UHFFFAOYSA-I pentasodium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical class [Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O HWGNBUXHKFFFIH-UHFFFAOYSA-I 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 238000005507 spraying Methods 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 4
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 4
- 239000010452 phosphate Substances 0.000 description 4
- 235000011007 phosphoric acid Nutrition 0.000 description 4
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical class [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 4
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 4
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 4
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000001354 calcination Methods 0.000 description 3
- 235000011180 diphosphates Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229940048086 sodium pyrophosphate Drugs 0.000 description 3
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- ZJIPHXXDPROMEF-UHFFFAOYSA-N dihydroxyphosphanyl dihydrogen phosphite Chemical class OP(O)OP(O)O ZJIPHXXDPROMEF-UHFFFAOYSA-N 0.000 description 2
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 229940048084 pyrophosphate Drugs 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000001488 sodium phosphate Substances 0.000 description 2
- UGTZMIPZNRIWHX-UHFFFAOYSA-K sodium trimetaphosphate Chemical compound [Na+].[Na+].[Na+].[O-]P1(=O)OP([O-])(=O)OP([O-])(=O)O1 UGTZMIPZNRIWHX-UHFFFAOYSA-K 0.000 description 2
- 239000011343 solid material Substances 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000011008 sodium phosphates Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- OBSZRRSYVTXPNB-UHFFFAOYSA-N tetraphosphorus Chemical compound P12P3P1P32 OBSZRRSYVTXPNB-UHFFFAOYSA-N 0.000 description 1
- 235000011178 triphosphate Nutrition 0.000 description 1
- 239000001226 triphosphate Substances 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B25/00—Phosphorus; Compounds thereof
- C01B25/16—Oxyacids of phosphorus; Salts thereof
- C01B25/26—Phosphates
- C01B25/38—Condensed phosphates
- C01B25/40—Polyphosphates
- C01B25/41—Polyphosphates of alkali metals
- C01B25/412—Preparation from alkali metal orthophosphates
Definitions
- the present invention relates to a process for the production of alkali metal polyphosphates having a bulk weight lower than that of polyphosphates produced by a known process.
- alkali metal polyphosphates such as sodium pyrophosphates or sodium triphosphates
- alkali metal polyphosphates are prepared by mixing orthophosphates in an appropriate proportion and treating the resulting mixture by applying heat.
- products with considerably varying bulk weights are obtained.
- processes have been developed to enable the production of polyphosphates having a low bulk weight.
- the aqueous orthophosphate solution necessary for the production of polyphosphates be first spray-dried and then calcined to yield a voluminous pulverulent or granular product, whose bulk weight naturally depends severely on how the spraying operation and calcination have been performed.
- alkali metal polyphosphates having a bulk weight of between about 250 grams/liter and about 600 grams/liter are obtained by heating at least one mono or di-alkali metal orthophosphate to a temperature of between about 200 C. and about 500 C. in the presence of about 0.03 weight percent to about 5 weight percent of an alkali metal salt derived from acids of phosphorus in which the phosphorus has an electropositive valency of less than five.
- the percentage figures given for these alkali metal salts are calculated upon the quantity of the alkali metal orthophosphate used. It should be noted that the alkali metal polyphosphates produced according to this invention have a bulk weight which is considerably lower than that of a polyphosphate produced by a known process.
- alkali metal salts of phosphorous acid As appropriate salts derived from acids of phosphorus in which the phosphorus has an electro-positive valency of less than five, there may be used the alkali metal salts of phosphorous acid or the alkali metal salts of hypophosphorous acid.
- alkali metal salt of phosphorous acid it is advisable to use the sodium phosphite and as alkali metal salt of hypophosphorous acid the sodium hypophosphite.
- the potassium alkali metal salts of this definition are also appropriate salts.
- a mixture of alkali metal salts of phosphorous acid and hypophosphorous acid at a ratio of the first to the second component of between about 0% and about or, inversely, between about 100% and about 0%, the first component being represented by the alkali metal salts of phosphorous acid and the second component by the alkali metal salts of hypophosphorous acid.
- These salts may be present as .already mentioned above in a total amount of between about 0.03 weight percent and about 5 weight percent calculated upon the quantity of alkali metal orthophosphate.
- this mixture be composed of sodium phosphite and sodium hypophosphite as alkali metal salts of phosphorous acid or hypophosphorous acid, respectively.
- the process of this invention enables for the first time, for example pure sodium triphosphate with a low bulk weight of up to 250 grams/ liter to be produced which is used for the production of uniform washing agents not liable to disintegration, for example, by mixing the above substance in a dry state with a spray-dried surface-active substance, for example sulfonates having a similar bulk weight.
- the alkali metal orthophosphates may be used in solution and, more especially in an aqueous solution, i.e., in a saturated or dilute aqueous solution.
- an aqueous solution i.e., in a saturated or dilute aqueous solution.
- alkali metal salts of phosphorous acid and/or hypophosphorous acid has proved especially effective, if the polyphosphates are prepared in a device which gives rise to the formation of a less heavy substance, i.e. by spraying an aqueous solution of the starting material in the hot at a temperature between about 200 C. and about 500 C. and then calcining at that temperature the resulting solid and only incompletely anhydrous substance.
- the spraying operation yields a solid material with a maximum water content of about 20% which is calcined and then completely anhydrous.
- alkali metal phosphites or alkali metal hypophos phites are especially readily accessible.
- the same effect may, however, be brought about using alkali metal salts of an acid other than phosphorous acid or hypophos phorous acid, in which the phosphorus has an electropositive valency of less than five; in other words, in addition to the aforesaid alkali metal salts of phosphorous acid and hypophosphorous acid there may also be used the alkali metal salts of pyrophosphorous acid or diphosphorous acid.
- These latter acids appear, for example in the hydrolysates of phosphorus trihalides in addition to phosphorous acid and it has been found that all reducing phosphorus compounds present in such hydrolysates play an essential part in bringing about a bulk weight reducing effect.
- a suitable addition may be prepared in simple manner from a technical and economical point of view by reacting yellow phosphorus with a boiling solution of sodium hydroxide.
- concentration of this solution may vary within wide limits, a solution of about 30% strength being, however, preferred.
- sodium phosphite and sodium hypophosphite are formed side by side in the solution.
- gaseous phosphorus hydride is evolved.
- the reaction proceeds in an especially favorphorus with the sodium hydroxide solution, it is necessary to use the latter component in an excess quantity of at least 20%. The higher the excess quantity, the more rapidly proceeds the reaction.
- the sodium hydroxide solution in excess may be neutralized with the use of phosphoric acid after the reaction is complete.
- the mixture of sodium phosphite and, sodium hypophosphite optionally in admixture with the sodium phosphate obtained by neutralizing the sodium hydroxide solution in excess with phosphoric acid, is added in a desired proportion to the ortho-phosphates which serve to yield the polyphosphates. It is understood that a mixture of salts of reducing acids of phosphorus naturally has the same effect as a uniform addition, such as phosphite or hypophosphite.
- the process of this invention offers the particular advantage of enabling the same industrial apparatus and the same operating procedures to be applied in the production of polyphosphates whose bulk weights may vary within wide limits depending on the quantity of the substances added.
- Example 1 For the production of sodium trimetaphosphate 500 grams of pulverulent dry and mono sodium orthophosphate are slowly heated to 480 C. in a rotary drum and kept 'at that temperature for 7 hours. The reaction yields 420 grams of a loose agglomerate which consists of 95% of sodium trimetaphosphate and can be comminuted to give a powder with a bulk weight of about 57 grams. liter.
- Example 2 To produce sodium triphosphate, a solution-is prepared at 80-100 C. which contains per liter of water 600 grams of Na i-IP0 and 253.5 grams of Nali-I PO The solution so prepared is spray-dried at a rate of 200 liters/ hour; the dry powder is then calcined for 10 minutes at 350 C. in a rotary drum. Sodium tn'phosphate is obtained in a yield of 150-160 kg./hour with a relatively high bulk weight of 650-700 grams/liter. The yield is 99-l00%.
- reaction conditions are the same with the exception, however, that per liter of the above orthophosphate solution 6 grams of sodium phosphite (Na -HPO 5H O) are added in accordance with this invention. The addition corresponds to about 0.7%. Triphcsphate is obtained in a quantity of 150-160 kg./hour with a bulk weight of only 450-500 grams/ liter. The triphosphate is free from reducing agents and obtained in a yield of 99-100%.
- Example 3 A solution of Na HPO saturated at 80 C. which contains per liter 690 grams of di-sodium phosphate is dehydrated at 350-400 C. at a rate of 145 liters/hour by hot-spraying in a spray-(tower to produce sodium pyrophosphate in the form of hollow balls. Spraying is effected using a pressure nozzle at a pressure of liquid of 6 atmospheres (gauge). The yield per hour is 94 kg. of
- the grain size of the individual particles is about 0.2-0.5 mm.
- the yield is 100% and the pyrophosphate obtained has a bulk weight of about 530 grams/liter.
- the disodium phosphate solution is mixed with 0.5% of sodium phosphite -(Na HPO accordingto this. invention; the pyrophosphate is obtained with thesame degree of purity and yield.
- the reduced bulk weight is only 400 grams/liter. If, however, 0.5% of sodium hypophosphite (NaH PO fio) is used instead of sodium phosphite, the sodium pyrophosphate is obtained in the form of hollow balls with the same degree of purity and in the same yield. The reduced bulk weight is in this case only-380 grams/liter.
- NaH PO fio sodium hypophosphite
- Example 4 For the production of sodium tripolyphosphate a solution is prepared at -100" C. which contains per liter 600 grams of Na HPO and 253.5 grams of Nail-1 1 0 Thissolution is sprayed in the hot at 400-450 C. at a rate of about 300 liters/hour to be converted into sodium tripolyphosphate which is obtained in a yield of about 230 kg. hour with a bulk weight of 600-620 grams/ liter.
- tripolyphosphate obtained has a bulk weight of 580-600 grams/ liter; in spite of. this minor addition the bulk weight is lower than that of a tripolyphosphate produced without such addition.
- thestarting ortho-i phosphate solution is mixed, per liter with 50.0 grams of Na HPO corresponding to an addition of about 6%.
- the tripolyphosphate obtained again has a bulk weight of 250-270 grams/ liter.
- Example 5 A solution of sodium phosphite (Na i-IP0 and-sodium hypophosphite suitable as addition may be prepared as follows:
- the water evaporating upon boiling is replaced.
- the reaction is complete within about 90 minutes.
- 7240 grams of sodium phosphite in addition to 795 grams of sodium hypophosphite and an excess quantity of sodium hydroxide solution.
- the reaction product obtained in the form of an aqueous solution has about the following composition after the sodium hydroxide solution present in excess has been neutralized with about 430 grams of a phosphoric acid: 7240 grams of Nat l-IP0 795 grams of NaH PO 510 grams of Na HPO and 10,055 grams of H 0.
- the solution so obtained is then added under the hollow balls of sodium pyrophosphate having a purity of :15 conditions described in Example 2 to 2400 liters of an orthophosphate solution and the whole is processed as described in that example.
- the sodium triphosphate is obtained in the same yield and has a reduced bulk weight of only 450-500 grams/liter.
- a process for the production of alkali metal polyphosphates having a bulk weight of between about 250 grams and about 600 grams per liter which comprises heating at least one alkali metal orthophosphate selected from the group consisting of mono-alkali metal orthophosphate and di-alkali metal orthophosphate to temperatures between about 200 C. and about 500 C. in the presence of about 0.03 to about 5 percent of an alkali metal salt of at least one acid of phosphorus selected from the group consisting of phosphorous acid and hypophosphorous acid, the percentage amount of alkali metal salt being calculated upon the quantity of alkali metal orthophosphate present, and recovering alkali metal polyphosphates having a bulk weight of between 250 and about 600 grams per liter.
- a process for the production of alkali metal polyphosphates having a bulk weight of between about 250 grams/liter and about 600 grams/liter which comprises heating at least one alkali metal orthophosphate selected from the group consisting of mono-alkali metal orthophosphate and di-alkali metal orthophosphate to a temperature of between about 200 C. and about 500 C. in the presence of about 0.03 to about 5 percent of sodium phosphite, the amount of alkali metal salt being calculated upon the quantity of the alkali metal orthophosphate present, and recovering alkali metal polyphosphates having a bulk weight of between 250-600 grams/ liter.
- a process for the production of alkali metal polyphosphates having a bulk weight of between about 250 grams/liter and about 600 grams/liter which comprises heating at least one alkali metal orthophosphate selected from the group consisting of mono-alkali metal orthophosphate and di-alkali metal orthophosphate to a temperature between about 200 C. and about 500 C. in the presence of about 0.03 to about 5 percent of sodium hypophosphite, the percentage amount of alkali metal salt being calculated upon the quantity of the alkali metal orthophosphate present, and recovering alkali metal polyphosphates having a bulk weight of between about 250- 600 grams/liter.
- a process for the production of alkali metal polyphosphates having a bulk weight of between about 250 grams/liter and about 600 grams/liter which comprises heating at least one alkali metal orthophosphate selected from the group consisting of mono-alkali metal orthophosphate and di-alkali metal orthophosphate to a temperature of between about 200 C. and about 500 C. in the presence of about 0.03 to about 5 percent of a mixture of sodium phosphite and sodium hypophosphite, the percentage amount of the mixture of alkali metal salts being calculated upon the quantity of alkali metal orthophosphate present, and recovering alkali metal polyphosphates having a bulk weight of between about 250-600 grams/liter.
- a process for the production of alkali metal polyphosphates having a bulk weight of between 380 grams/liter and about 400 grams/liter which comprises heating at least one alkali metal orthophosphate selected from the group consisting of mono-alkali metal orthophosphate and di-alkali metal orthophosphate to a temperature between about 200 C. and about 500 C. in the presence of about 0.5 percent of an alkali metal salt of at least one acid of phosphorus selected from the group consisting of phosphorous acid and hypophosphorous acid, the percentage amount of alkali metal salt being calculated upon the quantity of alkali metal orthophosphate present, and recovering alkali metal polyphosphates having a bulk weight between 380 and 400 grams/liter.
- a process for the production of alkali metal polyphosphates having a bulk weight of between about 380 grams/liter and about 400 grams/liter which comprises heating a solution containing at least one alkali metal orthophosphate selected from the group consisting of mono-alkali metal orthophosphate and di-alkali metal orthophosphate to a temperature between about 200 C. and about 500 C. in the presence of about 0.5 percent of a dissolved alkali metal salt of at least one acid of phosphorus selected from the group consisting of phosphorous acid and hypophosphorous acid, the percentage amount of alkali metal salt being calculated upon the quantity of the alkali metal orthophosphate present, atomizing resulting solution at a temperature of between about 200 C. and about 500 C., and calcining resulting solid material at a temperature of about 200 C. to about 500 C., and recovering alkali metal polyphosphates having a bulk weight of between about 280-400 grams/liter.
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Description
United States Patent PROCESS FOR THE PRODUCTION OF ALKALI lWETAL POLYPHOSPHATES Franz Rodis and Klaus Beltz, Knapsack, near Koln, Germany, assignors to Knapsack-Griesheim Aktiengesellschaft, Knapsack, near Koln, Germany, a corporation of Germany No Drawing. Filed Nov. 7, 1956, Ser. No. 620,820
Claims priority, application Germany Nov. 10, 1955 10 Claims. (Cl. 23-106) The present invention relates to a process for the production of alkali metal polyphosphates having a bulk weight lower than that of polyphosphates produced by a known process.
It is known that alkali metal polyphosphates, such as sodium pyrophosphates or sodium triphosphates, are prepared by mixing orthophosphates in an appropriate proportion and treating the resulting mixture by applying heat. Depending on the reaction conditions applied in each particular case, products with considerably varying bulk weights are obtained. Accordingly, processes have been developed to enable the production of polyphosphates having a low bulk weight. Thus, for example, it has been suggested that the aqueous orthophosphate solution necessary for the production of polyphosphates be first spray-dried and then calcined to yield a voluminous pulverulent or granular product, whose bulk weight naturally depends severely on how the spraying operation and calcination have been performed.
It has been found however that the bulk weights obtainable in the manner described above are not sufiiciently low to be satisfactory in certain application fields of the polyphosphates. It has also been found that it is extremely difiicult to produce a phosphate with a low bulk weight, especially in the case where the phosphate must be completely dehydrated. A sodium triphosphate containing residues of acid pyrophosphates or orthophosphates, for example, has a lower bulk weight than completely dehydrated Na P O of 98-l0 0% strength produced in the same manner.
Now we have found that alkali metal polyphosphates having a bulk weight of between about 250 grams/liter and about 600 grams/liter are obtained by heating at least one mono or di-alkali metal orthophosphate to a temperature of between about 200 C. and about 500 C. in the presence of about 0.03 weight percent to about 5 weight percent of an alkali metal salt derived from acids of phosphorus in which the phosphorus has an electropositive valency of less than five. The percentage figures given for these alkali metal salts are calculated upon the quantity of the alkali metal orthophosphate used. It should be noted that the alkali metal polyphosphates produced according to this invention have a bulk weight which is considerably lower than that of a polyphosphate produced by a known process.
In practising the process of this invention there may be used especially sodium orthophosphate and potassium orthophosphate and other alkali metal salts.
As appropriate salts derived from acids of phosphorus in which the phosphorus has an electro-positive valency of less than five, there may be used the alkali metal salts of phosphorous acid or the alkali metal salts of hypophosphorous acid. As alkali metal salt of phosphorous acid it is advisable to use the sodium phosphite and as alkali metal salt of hypophosphorous acid the sodium hypophosphite. The potassium alkali metal salts of this definition, however, are also appropriate salts.
ice
In the process of this invention there may also be used a mixture of alkali metal salts of phosphorous acid and hypophosphorous acid at a ratio of the first to the second component of between about 0% and about or, inversely, between about 100% and about 0%, the first component being represented by the alkali metal salts of phosphorous acid and the second component by the alkali metal salts of hypophosphorous acid.
These salts may be present as .already mentioned above in a total amount of between about 0.03 weight percent and about 5 weight percent calculated upon the quantity of alkali metal orthophosphate.
In carrying out the process of this invention on an industrial scale using a mixture of the above type it is advisable that this mixture be composed of sodium phosphite and sodium hypophosphite as alkali metal salts of phosphorous acid or hypophosphorous acid, respectively.
The process of this invention enables for the first time, for example pure sodium triphosphate with a low bulk weight of up to 250 grams/ liter to be produced which is used for the production of uniform washing agents not liable to disintegration, for example, by mixing the above substance in a dry state with a spray-dried surface-active substance, for example sulfonates having a similar bulk weight.
According to another feature of this invention, the alkali metal orthophosphates may be used in solution and, more especially in an aqueous solution, i.e., in a saturated or dilute aqueous solution. For economical reasons, however, it is advisable to use a fairly concentrated solution.
The addition of alkali metal salts of phosphorous acid and/or hypophosphorous acid has proved especially effective, if the polyphosphates are prepared in a device which gives rise to the formation of a less heavy substance, i.e. by spraying an aqueous solution of the starting material in the hot at a temperature between about 200 C. and about 500 C. and then calcining at that temperature the resulting solid and only incompletely anhydrous substance.
The spraying operation yields a solid material with a maximum water content of about 20% which is calcined and then completely anhydrous.
Especially suitable additions as already described above are alkali metal phosphites or alkali metal hypophos phites, for they are most readily accessible. The same effect may, however, be brought about using alkali metal salts of an acid other than phosphorous acid or hypophos phorous acid, in which the phosphorus has an electropositive valency of less than five; in other words, in addition to the aforesaid alkali metal salts of phosphorous acid and hypophosphorous acid there may also be used the alkali metal salts of pyrophosphorous acid or diphosphorous acid. These latter acids appear, for example in the hydrolysates of phosphorus trihalides in addition to phosphorous acid and it has been found that all reducing phosphorus compounds present in such hydrolysates play an essential part in bringing about a bulk weight reducing effect.
A suitable addition may be prepared in simple manner from a technical and economical point of view by reacting yellow phosphorus with a boiling solution of sodium hydroxide. The concentration of this solution may vary within wide limits, a solution of about 30% strength being, however, preferred. During this reaction, sodium phosphite and sodium hypophosphite are formed side by side in the solution. In addition, gaseous phosphorus hydride is evolved. The reaction proceeds in an especially favorphorus with the sodium hydroxide solution, it is necessary to use the latter component in an excess quantity of at least 20%. The higher the excess quantity, the more rapidly proceeds the reaction. The sodium hydroxide solution in excess may be neutralized with the use of phosphoric acid after the reaction is complete.
The mixture of sodium phosphite and, sodium hypophosphite optionally in admixture with the sodium phosphate obtained by neutralizing the sodium hydroxide solution in excess with phosphoric acid, is added in a desired proportion to the ortho-phosphates which serve to yield the polyphosphates. It is understood that a mixture of salts of reducing acids of phosphorus naturally has the same effect as a uniform addition, such as phosphite or hypophosphite.
All these compounds which serve to reduce the bulk weight according to this invention are heated together with the acid orthophosphates to form salts of pentavalent phosphorus. The polyphosphate obtained as end product is free from reducing ingredients.
The process of this invention offers the particular advantage of enabling the same industrial apparatus and the same operating procedures to be applied in the production of polyphosphates whose bulk weights may vary within wide limits depending on the quantity of the substances added.
It has been found that already theraddition of the above substances in an amount of 0.03% to the orthophosphates may involve a minor reducing efiect on the bulk weight. Larger amounts than 0.03% reduce the bulk weight further; an amount exceeding 5% involves however no further noteworthy effect.
The following examples serve to illustrate the invention but they are not intended to limit it thereto. These examples clearly evidence the advance achieved in the art by this new process especially with reference to the conventional working method.
Example 1 For the production of sodium trimetaphosphate 500 grams of pulverulent dry and mono sodium orthophosphate are slowly heated to 480 C. in a rotary drum and kept 'at that temperature for 7 hours. The reaction yields 420 grams of a loose agglomerate which consists of 95% of sodium trimetaphosphate and can be comminuted to give a powder with a bulk weight of about 57 grams. liter.
When the same reaction is carried out according to this invention, i.e. with the addition of 1% of sodium phosphite, the bulk weight is considerably reduced to about 460- grams/liter. The yield is about 99%.
Example 2 To produce sodium triphosphate, a solution-is prepared at 80-100 C. which contains per liter of water 600 grams of Na i-IP0 and 253.5 grams of Nali-I PO The solution so prepared is spray-dried at a rate of 200 liters/ hour; the dry powder is then calcined for 10 minutes at 350 C. in a rotary drum. Sodium tn'phosphate is obtained in a yield of 150-160 kg./hour with a relatively high bulk weight of 650-700 grams/liter. The yield is 99-l00%.
The reaction conditions are the same with the exception, however, that per liter of the above orthophosphate solution 6 grams of sodium phosphite (Na -HPO 5H O) are added in accordance with this invention. The addition corresponds to about 0.7%. Triphcsphate is obtained in a quantity of 150-160 kg./hour with a bulk weight of only 450-500 grams/ liter. The triphosphate is free from reducing agents and obtained in a yield of 99-100%.
Example 3 A solution of Na HPO saturated at 80 C. which contains per liter 690 grams of di-sodium phosphate is dehydrated at 350-400 C. at a rate of 145 liters/hour by hot-spraying in a spray-(tower to produce sodium pyrophosphate in the form of hollow balls. Spraying is effected using a pressure nozzle at a pressure of liquid of 6 atmospheres (gauge). The yield per hour is 94 kg. of
4 98-100%. The grain size of the individual particles is about 0.2-0.5 mm. The yield is 100% and the pyrophosphate obtained has a bulk weight of about 530 grams/liter.
While the conditions are otherwise identical, the disodium phosphate solution is mixed with 0.5% of sodium phosphite -(Na HPO accordingto this. invention; the pyrophosphate is obtained with thesame degree of purity and yield.
The reduced bulk weight is only 400 grams/liter. If, however, 0.5% of sodium hypophosphite (NaH PO fio) is used instead of sodium phosphite, the sodium pyrophosphate is obtained in the form of hollow balls with the same degree of purity and in the same yield. The reduced bulk weight is in this case only-380 grams/liter.
Example 4 For the production of sodium tripolyphosphate a solution is prepared at -100" C. which contains per liter 600 grams of Na HPO and 253.5 grams of Nail-1 1 0 Thissolution is sprayed in the hot at 400-450 C. at a rate of about 300 liters/hour to be converted into sodium tripolyphosphate which is obtained in a yield of about 230 kg. hour with a bulk weight of 600-620 grams/ liter. The
yield is 99-100% While the conditions are identical, 0.25 gram of Na 'HPO is added per liter of the orthophosphate solution; the addition corresponds to 0.03%. The tripolyphosphate obtained has a bulk weight of 580-600 grams/ liter; in spite of. this minor addition the bulk weight is lower than that of a tripolyphosphate produced without such addition.
While the conditions are identical, the starting solution of orthophosphates is mixed per liter with 42.7 grams of Na HPO correspondingto an addition of 5%. :The tripolyphosphate obtained has a bulk weight of only 250- 270 grams/ liter.
While the conditions are the same, thestarting ortho-i phosphate solution is mixed, per liter with 50.0 grams of Na HPO corresponding to an addition of about 6%. The tripolyphosphate obtained again has a bulk weight of 250-270 grams/ liter.
The above example clearly evidences that already a very small addition of Na HPO reduces the bulk weight, while the upper limit of such additions is about 5% outside which no further reduction of the bulk weight which is as low as 250 grams/liter can be achieved, so thatan addition of more than 5% of substances reducing the bulk weight is useless.
Example 5 A solution of sodium phosphite (Na i-IP0 and-sodium hypophosphite suitable as addition may be prepared as follows:
3 kg. of yellow phosphors are introduced into 17.5 kg.-
of a boiling 30% sodium hydroxide solution. A vigorous reaction sets in with evolution of phosphorus hydride which is calcined with air to form phosphorus pentoxide; the phosphorus pentoxide is then introduced into anapparatus suitable for use in the production of ortho-phosphoric acid.
The water evaporating upon boiling is replaced. The reaction is complete within about 90 minutes. In the aqueous phase there are obtained 7240 grams of sodium phosphite in addition to 795 grams of sodium hypophosphite and an excess quantity of sodium hydroxide solution. The reaction product obtained in the form of an aqueous solution has about the following composition after the sodium hydroxide solution present in excess has been neutralized with about 430 grams of a phosphoric acid: 7240 grams of Nat l-IP0 795 grams of NaH PO 510 grams of Na HPO and 10,055 grams of H 0. The solution so obtained is then added under the hollow balls of sodium pyrophosphate having a purity of :15 conditions described in Example 2 to 2400 liters of an orthophosphate solution and the whole is processed as described in that example. The sodium triphosphate is obtained in the same yield and has a reduced bulk weight of only 450-500 grams/liter.
We claim:
1. A process for the production of alkali metal polyphosphates having a bulk weight of between about 250 grams and about 600 grams per liter, which comprises heating at least one alkali metal orthophosphate selected from the group consisting of mono-alkali metal orthophosphate and di-alkali metal orthophosphate to temperatures between about 200 C. and about 500 C. in the presence of about 0.03 to about 5 percent of an alkali metal salt of at least one acid of phosphorus selected from the group consisting of phosphorous acid and hypophosphorous acid, the percentage amount of alkali metal salt being calculated upon the quantity of alkali metal orthophosphate present, and recovering alkali metal polyphosphates having a bulk weight of between 250 and about 600 grams per liter.
2. The process of claim 1 wherein sodium orthophosphate and a sodium salt of at least one acid of phosphorus selected from the group consisting of phosphorous acid and hypophosphorous acid are heated.
3. The process of claim 1 wherein potassium orthophosphate and a potassium salt of at least one acid of phosphorus selected from the group consisting of phosphorous acid and hypophosphorous acid are heated.
4. The process of claim 1 wherein an aqueous solution of at least one alkali metal orthophosphate selected from the group consisting of mono-alkali metal orthophosphate and di-alkali metal orthophosphate and about 0.03 to about 5 percent of a dissolved alkali metal salt of at least one acid of phosphorus selected from the group consisting of phosphorous acid and hypophosphorous acid are heated.
5. The process of claim 4 wherein the aqueous solution is atomized at a temperature between about 200 C. and about 500 C. and the resulting solid product is calcined at a temperature between about 200 C. and about 500 C.
6. A process for the production of alkali metal polyphosphates having a bulk weight of between about 250 grams/liter and about 600 grams/liter which comprises heating at least one alkali metal orthophosphate selected from the group consisting of mono-alkali metal orthophosphate and di-alkali metal orthophosphate to a temperature of between about 200 C. and about 500 C. in the presence of about 0.03 to about 5 percent of sodium phosphite, the amount of alkali metal salt being calculated upon the quantity of the alkali metal orthophosphate present, and recovering alkali metal polyphosphates having a bulk weight of between 250-600 grams/ liter.
7. A process for the production of alkali metal polyphosphates having a bulk weight of between about 250 grams/liter and about 600 grams/liter which comprises heating at least one alkali metal orthophosphate selected from the group consisting of mono-alkali metal orthophosphate and di-alkali metal orthophosphate to a temperature between about 200 C. and about 500 C. in the presence of about 0.03 to about 5 percent of sodium hypophosphite, the percentage amount of alkali metal salt being calculated upon the quantity of the alkali metal orthophosphate present, and recovering alkali metal polyphosphates having a bulk weight of between about 250- 600 grams/liter.
8. A process for the production of alkali metal polyphosphates having a bulk weight of between about 250 grams/liter and about 600 grams/liter which comprises heating at least one alkali metal orthophosphate selected from the group consisting of mono-alkali metal orthophosphate and di-alkali metal orthophosphate to a temperature of between about 200 C. and about 500 C. in the presence of about 0.03 to about 5 percent of a mixture of sodium phosphite and sodium hypophosphite, the percentage amount of the mixture of alkali metal salts being calculated upon the quantity of alkali metal orthophosphate present, and recovering alkali metal polyphosphates having a bulk weight of between about 250-600 grams/liter.
9. A process for the production of alkali metal polyphosphates having a bulk weight of between 380 grams/liter and about 400 grams/liter which comprises heating at least one alkali metal orthophosphate selected from the group consisting of mono-alkali metal orthophosphate and di-alkali metal orthophosphate to a temperature between about 200 C. and about 500 C. in the presence of about 0.5 percent of an alkali metal salt of at least one acid of phosphorus selected from the group consisting of phosphorous acid and hypophosphorous acid, the percentage amount of alkali metal salt being calculated upon the quantity of alkali metal orthophosphate present, and recovering alkali metal polyphosphates having a bulk weight between 380 and 400 grams/liter.
10. A process for the production of alkali metal polyphosphates having a bulk weight of between about 380 grams/liter and about 400 grams/liter which comprises heating a solution containing at least one alkali metal orthophosphate selected from the group consisting of mono-alkali metal orthophosphate and di-alkali metal orthophosphate to a temperature between about 200 C. and about 500 C. in the presence of about 0.5 percent of a dissolved alkali metal salt of at least one acid of phosphorus selected from the group consisting of phosphorous acid and hypophosphorous acid, the percentage amount of alkali metal salt being calculated upon the quantity of the alkali metal orthophosphate present, atomizing resulting solution at a temperature of between about 200 C. and about 500 C., and calcining resulting solid material at a temperature of about 200 C. to about 500 C., and recovering alkali metal polyphosphates having a bulk weight of between about 280-400 grams/liter.
References Cited in the file of this patent UNITED STATES PATENTS 2,174,614 Bornemann et a1. Oct. 3, 1939 2,182,357 Schwartz Dec. 5, 1939 2,776,187 Pfrengle Jan. 1, 1957 FOREIGN PATENTS 441,474 Great Britain Jan. 20, 1936 495,192 Great Britain Nov. 8, 1938 OTHER REFERENCES Van Wazer: Phosphorus and Its Compounds, vol. 1, Chemistry, Inter-Science, 1958, page 569.
Zeitschrift fiir Anorganische Chemie, Rosenheim et al., vol. 129 (1 923), pages 196-206.
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 2,986,449 May 30, 1961 Franz Rodis et al.
It is hereby certified -that error appears in the above numbered patent requiring correction and that the said Letters Patent. should read as "corrected below.
Column 6, line 47 for "280-400" read 380-400 Signed and sealed this 14th day of November 1961 a (SEAL) Attest:
ERNEST W. SWIDER DAVID L. LADD Attesting Officer Commissioner of Patents USCOMM-DC-
Claims (1)
1. A PROCESS FOR THE PRODUCTION OF ALKALI METAL POLYPHOSPHATES HAVING A BULK WEIGHT OF BETWEEN ABOUT 250 GRAMS AND ABOUT 600 GRAMS PER LITER, WHICH COMPRISES HEATING AT LEAST ONE ALKALI METAL ORTHOPHOSPHATE SELECTED FROM THE GROUP CONSISTING OF MONO-ALKALI METAL ORTHOPHOSPHATE AND DI-ALKALI METAL ORTHOPHOSPHATE TO TEMPERATURES BETWEEN ABOUT 200*C. AND ABOUT 500*C. IN THE PRESENCE OF ABOUT 0.03 TO ABOUT 5 PERCENT OF AN ALKALI METAL SALT OF AT LEAST ONE ACID OF PHOSPHORUS SELECTED FROM THE GROUP CONSISTING OF PHOSPHOROUS ACID AND HYPOPHOSPHOROUS ACID, THE PERCENTAGE AMOUNT OF ALKALI METAL SALT BEING CALCUALTED UPON THE QUANTITY OF ALKALI METAL ORHOPHOSPHATE PRESENT, AND RECOVERING ALKALI METAL POLYPHOSPHATES HAVING A BULK WEIGHT OF BETWEEN 250 AND ABOUT 600 GRAMS PER LITER.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2986449X | 1955-11-10 |
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| Application Number | Title | Priority Date | Filing Date |
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| US620820A Expired - Lifetime US2986449A (en) | 1955-11-10 | 1956-11-07 | Process for the production of alkali metal polyphosphates |
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Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3210154A (en) * | 1962-03-07 | 1965-10-05 | Stauffer Chemical Co | Molecularly dehydrated phosphates |
| US3230039A (en) * | 1962-01-02 | 1966-01-18 | Monsanto Co | Process for manufacturing sodium trimetaphosphate products |
| US3230041A (en) * | 1962-11-29 | 1966-01-18 | Monsanto Co | Method for making tetra-alkali metal pyrophosphate |
| US3278328A (en) * | 1963-09-16 | 1966-10-11 | Exxon Research Engineering Co | Method of coating substrates with inorganic polyphosphates |
| US3378341A (en) * | 1962-11-27 | 1968-04-16 | Knapsack Ag | Process for the manufacture of polyphosphates of low bulk density |
| US3449068A (en) * | 1966-02-09 | 1969-06-10 | Knapsack Ag | Process for the manufacture of polyphosphates |
| US3869317A (en) * | 1971-12-08 | 1975-03-04 | Joachim Marx | Producing protective coatings on metal |
| EP0199139A2 (en) * | 1985-04-17 | 1986-10-29 | Hoechst Aktiengesellschaft | Process ad apparatus for the manufacture of alkali metalpolyphosphates in the form of hollow spheres having a low apparent density |
| EP0199140A2 (en) * | 1985-04-17 | 1986-10-29 | Hoechst Aktiengesellschaft | Hollow ball shaped alkaline polyphosphate with a low apparent density, method and installation for its preparation |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB441474A (en) * | 1934-06-19 | 1936-01-20 | Henkel & Cie Gmbh | Improved manufacture of polyphosphates |
| GB495192A (en) * | 1936-04-11 | 1938-11-08 | Huels Chemische Werke Ag | Process for the manufacture of polyphosphates |
| US2174614A (en) * | 1936-04-09 | 1939-10-03 | Bornemann Ferdinand | Method of producing polyphosphates and polyphosphate mixtures |
| US2182357A (en) * | 1937-06-17 | 1939-12-05 | Hall Lab Inc | Manufacture of casein products |
| US2776187A (en) * | 1950-09-08 | 1957-01-01 | Chem Fab Budenheim Ag | Production of tripolyphosphates |
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1956
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Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB441474A (en) * | 1934-06-19 | 1936-01-20 | Henkel & Cie Gmbh | Improved manufacture of polyphosphates |
| US2174614A (en) * | 1936-04-09 | 1939-10-03 | Bornemann Ferdinand | Method of producing polyphosphates and polyphosphate mixtures |
| GB495192A (en) * | 1936-04-11 | 1938-11-08 | Huels Chemische Werke Ag | Process for the manufacture of polyphosphates |
| US2182357A (en) * | 1937-06-17 | 1939-12-05 | Hall Lab Inc | Manufacture of casein products |
| US2776187A (en) * | 1950-09-08 | 1957-01-01 | Chem Fab Budenheim Ag | Production of tripolyphosphates |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3230039A (en) * | 1962-01-02 | 1966-01-18 | Monsanto Co | Process for manufacturing sodium trimetaphosphate products |
| US3210154A (en) * | 1962-03-07 | 1965-10-05 | Stauffer Chemical Co | Molecularly dehydrated phosphates |
| US3378341A (en) * | 1962-11-27 | 1968-04-16 | Knapsack Ag | Process for the manufacture of polyphosphates of low bulk density |
| US3230041A (en) * | 1962-11-29 | 1966-01-18 | Monsanto Co | Method for making tetra-alkali metal pyrophosphate |
| US3278328A (en) * | 1963-09-16 | 1966-10-11 | Exxon Research Engineering Co | Method of coating substrates with inorganic polyphosphates |
| US3449068A (en) * | 1966-02-09 | 1969-06-10 | Knapsack Ag | Process for the manufacture of polyphosphates |
| US3869317A (en) * | 1971-12-08 | 1975-03-04 | Joachim Marx | Producing protective coatings on metal |
| EP0199139A2 (en) * | 1985-04-17 | 1986-10-29 | Hoechst Aktiengesellschaft | Process ad apparatus for the manufacture of alkali metalpolyphosphates in the form of hollow spheres having a low apparent density |
| EP0199140A2 (en) * | 1985-04-17 | 1986-10-29 | Hoechst Aktiengesellschaft | Hollow ball shaped alkaline polyphosphate with a low apparent density, method and installation for its preparation |
| EP0199139A3 (en) * | 1985-04-17 | 1988-03-02 | Hoechst Aktiengesellschaft | Alkali metal polyphosphates in the form of hollow spheres having a low apparent density, and process and apparatus for their manufacture |
| EP0199140A3 (en) * | 1985-04-17 | 1989-02-01 | Hoechst Aktiengesellschaft | Hollow ball shaped alkaline polyphosphate with a low apparent density, method and installation for its preparation |
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