ZA200106211B - Method for purification of phosphoric acid and high purity polyphosphoric acid. - Google Patents
Method for purification of phosphoric acid and high purity polyphosphoric acid. Download PDFInfo
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- ZA200106211B ZA200106211B ZA200106211A ZA200106211A ZA200106211B ZA 200106211 B ZA200106211 B ZA 200106211B ZA 200106211 A ZA200106211 A ZA 200106211A ZA 200106211 A ZA200106211 A ZA 200106211A ZA 200106211 B ZA200106211 B ZA 200106211B
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- phosphoric acid
- ppm
- content
- arsenic
- acid
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- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 title claims description 249
- 229910000147 aluminium phosphate Inorganic materials 0.000 title claims description 118
- 238000000034 method Methods 0.000 title claims description 93
- 229920000137 polyphosphoric acid Polymers 0.000 title claims description 64
- 238000000746 purification Methods 0.000 title claims description 21
- 229910052785 arsenic Inorganic materials 0.000 claims description 86
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 84
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 44
- 229910000039 hydrogen halide Inorganic materials 0.000 claims description 39
- 239000012433 hydrogen halide Substances 0.000 claims description 39
- 239000011734 sodium Substances 0.000 claims description 36
- 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 claims description 29
- 229910052708 sodium Inorganic materials 0.000 claims description 29
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical group Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 22
- 239000000377 silicon dioxide Substances 0.000 claims description 22
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 21
- 150000001875 compounds Chemical class 0.000 claims description 18
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims description 18
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims description 18
- 230000002378 acidificating effect Effects 0.000 claims description 14
- 239000011651 chromium Substances 0.000 claims description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 9
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 7
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 7
- 229910052804 chromium Inorganic materials 0.000 claims description 7
- 229910052750 molybdenum Inorganic materials 0.000 claims description 7
- 239000011733 molybdenum Substances 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 4
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims description 4
- IUTCEZPPWBHGIX-UHFFFAOYSA-N tin(2+) Chemical compound [Sn+2] IUTCEZPPWBHGIX-UHFFFAOYSA-N 0.000 claims description 4
- VMQMZMRVKUZKQL-UHFFFAOYSA-N Cu+ Chemical compound [Cu+] VMQMZMRVKUZKQL-UHFFFAOYSA-N 0.000 claims description 3
- 235000011007 phosphoric acid Nutrition 0.000 description 117
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 18
- 229910001385 heavy metal Inorganic materials 0.000 description 15
- 239000011521 glass Substances 0.000 description 12
- 239000007789 gas Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 9
- 238000004458 analytical method Methods 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 7
- 238000007664 blowing Methods 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 238000005345 coagulation Methods 0.000 description 7
- 230000015271 coagulation Effects 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 238000007796 conventional method Methods 0.000 description 6
- 238000001914 filtration Methods 0.000 description 6
- 238000005273 aeration Methods 0.000 description 5
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 5
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 150000001495 arsenic compounds Chemical class 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229910001507 metal halide Inorganic materials 0.000 description 4
- 150000005309 metal halides Chemical group 0.000 description 4
- -1 polyphosphoric acid Chemical compound 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 239000012776 electronic material Substances 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 238000009616 inductively coupled plasma Methods 0.000 description 3
- 238000006068 polycondensation reaction Methods 0.000 description 3
- 239000012488 sample solution Substances 0.000 description 3
- HYHCSLBZRBJJCH-UHFFFAOYSA-M sodium hydrosulfide Chemical compound [Na+].[SH-] HYHCSLBZRBJJCH-UHFFFAOYSA-M 0.000 description 3
- 229910052979 sodium sulfide Inorganic materials 0.000 description 3
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XPDICGYEJXYUDW-UHFFFAOYSA-N tetraarsenic tetrasulfide Chemical compound S1[As]2S[As]3[As]1S[As]2S3 XPDICGYEJXYUDW-UHFFFAOYSA-N 0.000 description 3
- GOLCXWYRSKYTSP-UHFFFAOYSA-N Arsenious Acid Chemical compound O1[As]2O[As]1O2 GOLCXWYRSKYTSP-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 2
- RBFQJDQYXXHULB-UHFFFAOYSA-N arsane Chemical compound [AsH3] RBFQJDQYXXHULB-UHFFFAOYSA-N 0.000 description 2
- 229910000070 arsenic hydride Inorganic materials 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 238000005342 ion exchange Methods 0.000 description 2
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 150000003388 sodium compounds Chemical class 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- OBSZRRSYVTXPNB-UHFFFAOYSA-N tetraphosphorus Chemical compound P12P3P1P32 OBSZRRSYVTXPNB-UHFFFAOYSA-N 0.000 description 2
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 2
- DJHGAFSJWGLOIV-UHFFFAOYSA-N Arsenic acid Chemical compound O[As](O)(O)=O DJHGAFSJWGLOIV-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 229940000488 arsenic acid Drugs 0.000 description 1
- COHDHYZHOPQOFD-UHFFFAOYSA-N arsenic pentoxide Chemical compound O=[As](=O)O[As](=O)=O COHDHYZHOPQOFD-UHFFFAOYSA-N 0.000 description 1
- 238000001479 atomic absorption spectroscopy Methods 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229920001429 chelating resin Polymers 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- KTTMEOWBIWLMSE-UHFFFAOYSA-N diarsenic trioxide Chemical compound O1[As](O2)O[As]3O[As]1O[As]2O3 KTTMEOWBIWLMSE-UHFFFAOYSA-N 0.000 description 1
- 150000004683 dihydrates Chemical class 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 230000000887 hydrating effect Effects 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000001603 reducing effect Effects 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
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- Silicon Compounds (AREA)
- Removal Of Specific Substances (AREA)
Description
SPECIFICATION
METHOD FOR PURIFICATION OF PHOSPHORIC ACID AND HIGH PURITY
POLYPHOSPHORIC ACID
The present invention relates to a method for purifying phosphoric acid, which can efficiently reduce the content of harmful heavy metal, particularly that of arsenic, and to high purity polyphosphoric acid obtained thereby, which is expected : to be applicable to a broader range of use in the fields of food, medicaments and electronic materials.
As a production method of phosphoric acid, there have been known a wet method and a dry method, and phosphoric acid is industrially produced by one of these methods. In the wet method, phosphorous ore is dissolved in sulfuric acid, a gypsum component is filtered off to produce dilute phosphoric acid having a low concentration, and the dilute phosphoric acid is concentrated to a desired level to give phosphoric acid. In the dry method, phosphorous ore is reduced in an electric furnace to give yellow phosphorus, which is burnt to give phosphoric anhydride, which is then hydrated to give phosphoric acid. In general, the wet method does not require reduction or combustion and is considered to be advantageous from the aspect of production cost. The dry method is considered to be advantageous from the aspect of quality, because the production via phosphoric anhydride reduces contamination of impurities derived from phosphorous ore. In any production method, however, the obtained phosphoric acid contains arsenic derived from phosphorous ore or phosphoric anhydride, which is harmful for oo human body, in generally about several dozen ppm, and the arsenic is removed by a sulfide coagulation method according to the use of the phosphoric acid. A conventional method for removing arsenic is applicable only to phosphoric acid having a
P,05 concentration of up to about 60%.
High concentration phosphoric acid, particularly
@ polyphosphoric acid (P,0s concentration of not less than 72.4%), is also produced by the aforementioned wet method or dry method, like phosphoric acid. Polyphosphoric acid produced by the dry method generally shows lower heavy metal, silica and sodium contents because the production goes through phosphoric anhydride. However, it contains arsenic derived from phosphoric anhydride in about 5-100 ppm, because a conventional method for removing arsenic cannot be applied to high concentration phosphoric acid. Polyphosphoric acid produced by the wet method shows a low arsenic content of less than 1 ppm because a conventional method for removing arsenic can be applied before concentration. On the other hand, it characteristically shows high contents of heavy metal, silica and sodium derived from phosphorous ore. High concentration phosphoric acid, particularly polyphosphoric acid, which characteristically shows a low arsenic content and low contents of heavy metal, silica and sodium, has not been obtained.
When phosphoric acid having a P,0s concentration of up to about 60%, which is obtained by a dry method, is subjected to a dearsenic treatment by a conventional sulfide coagulation method : and the like and concentrated, polyphosphoric acid having low contents of arsenic, heavy metal, silica and sodium is presumably obtained. However, such production method has not been put to practical use. This is because equipment for burning and hydrating yellow phosphorus and for highly concentrating the resulting phosphoric acid is required, which is extremely disadvantageous from the economical point of view, due to high facility costs and high operation costs.
The arsenic contained in phosphoric acid and polyphosphoric acid is particularly problematic for a use that requires high purity, in the fields of food, medicaments, electronic materials and the like. Given the high attention to the environmental problems in recent years, moreover, phosphoric acid and polyphosphoric acid having a low arsenic content are desired as industrial phosphoric acid to be used for metal
® surface treatment, dye processing and the like. Therefore, a method for removing arsenic, which affords efficient operation at lower costs, is demanded. :
Known methods for removing arsenic from phosphoric acid include (1) sulfide coagulation method, (2) solvent extraction method and (3) ion exchange method. Of these, the sulfide coagulation method is most popular because the required steps and equipment are rather simple and this method is operable at a low cost. This method includes bringing phosphoric acid into contact with hydrogen sulfide, or sodium sulfide, sodium hydrosulfide and the like, which produce hydrogen sulfide upon dissolution in phosphoric acid, to allow precipitation of arsenic as arsenic sulfide, which is followed by separation for removal. In contrast, the solvent extraction method and ion exchange method are less popular because of the complicated steps and complicated equipment, as well as higher costs. : | However, the sulfide coagulation method, too, requires filtration equipment, such as vacuum filter, press filter, centrifuge separator and the like. The precipitated arsenic sulfide tends to become a gel, which makes it difficult to separate and remove arsenic from phosphoric acid. For facilitated separation, a method (Japanese Unexamined
Publication No. 6-48712) comprising passage through an activated : carbon tower, and a method (Japanese Unexamined Publication No. 6-100307) comprising addition of a chelating resin are used. :
These methods are unpreferable because the facility and treatment costs become higher.
When hydrogen sulfide remains in phosphoric acid, moreover, corrosion of phosphoric acid is enhanced, thus necessitating deaeration of excess hydrogen sulfide with air or nitrogen, which in turn makes the step complicated. When compounds such as sodium sulfide, sodium hydrosulfide and the like are used, this method cannot be applied to a use where a sodium content matters, since sodium remains in a large amount in phosphoric acid. Co
In the case of the sulfide coagulation method, when the phosphoric acid concentration is high, particularly in the case : of polyphosphoric acid, phosphoric acid itself comes to have a higher viscosity, thereby making the separation for removal of arsenic sulfide more difficult. Therefore, this method is applicable to phosphoric acid having a P,05 concentration of about 60% at most. : The method for removing arsenic from phosphoric acid having a higher concentration is disclosed in Japanese Examined
Publication No. 53-128595 as the purification method of phosphoric acid by a wet method. According to this method, sodium chloride is added to phosphoric acid having a P,0s concentration of up to about 82% to allow reaction of arsenic in phosphoric acid with chlorine for separation and removal.
Because this method involves the use of sodium chloride in 1000- 2000 ppm, sodium remains in a great amount in phosphoric acid after removing arsenic. -
The conventional methods for removing arsenic require a filtration step and a deaeration step, both of which are costly, and sodium remains in a great amount in phosphoric acid. They cannot be applied to high concentration phosphoric acid having a
P,05 concentration of not less than 60%, particularly polyphosphoric acid. In addition, there has not been obtained high concentration phosphoric acid, particularly polyphosphoric acid, having lower contents of arsenic, heavy metal, silica and sodium, by a method operable at a low cost. Therefore, the : field of use of polyphosphoric acid has been limited to the field free of a high purity requirement.
The present invention provides a completely new method for removing arsenic from phosphoric acid, which is operable at a low cost, which requires no filtration step or deaeration step but is free of a large amount of residual sodium, unlike sulfide coagulation method, and which is applicable to high concentration phosphoric acid, particularly polyphosphoric acid.
In addition, the present invention aims at obtaining high purity polyphosphoric acid having low contents of arsenic, heavy .metal, silica and sodium, which has not been conventionally obtained.
The present inventors have conducted intensive studies in an attempt to solve the above-mentioned problems and found that the arsenic content of phosphoric acid drastically falls during an organic synthetic reaction accompanying production of hydrogen chloride in high concentration phosphoric acid.
Further investigation thereof has revealed that this organic synthetic reaction itself has nothing to do with an arsenic : removal effect but, by bringing phosphoric acid into contact with hydrogen halide, the arsenic content of phosphoric acid can be reduced to not more than about 1 ppm, that, when the contact is performed in the presence of a compound capable of generating _ hydrogen halide under acidic conditions, the arsenic removal effect is enhanced, and that this method is useful for removing arsenic particularly from polyphosphoric acid, which resulted in the completion of the present invention.
Accordingly, the present invention provides the following. (1) A method for purifying phosphoric acid, which comprises bringing phosphoric acid containing arsenic into contact with hydrogen halide, thereby to remove the arsenic from the phosphoric acid. . (2) The purification method of (1) above, wherein the phosphoric acid containing the arsenic is brought into contact with hydrogen halide in the presence of a compound capable of generating hydrogen halide under acidic conditions. (3) The purification method of (2) above, wherein the compound capable of generating hydrogen halide under acidic conditions is added in a proportion of less than 1 wt% of a weight of the phosphoric acid. (4) The purification method of (2) above, wherein the compound capable of generating hydrogen halide under acidic conditions is 35. a chloride of iron(II), copper(I) or tin(II).
(5) The purification method of (1) above, wherein the hydrogen halide is hydrogen chloride. (6) The purification method of (1) above, wherein the phosphoric acid has a P,05 concentration of not less than 72.4%. (7) A high purity polyphosphoric acid having an iron (Fe) content of not more than 20 ppm, a sodium (Na) content of not more than 100 ppm, a silica (SiO;) content of not more than 50 ppm and an arsenic (As) content of not more than 1 ppm. : (8) The high purity polyphosphoric acid of (7) above, wherein the iron (Fe) content is not more than 10 ppm, the sodium (Na) content is not more than 5 ppm, the silica (SiO,) content is not more than 5 ppm and the arsenic (As) content is not more than 1 oo ppm. (9) The high purity polyphosphoric acid of (7) above, which has a chromium (Cr) content of not more than 5 ppm, a nickel (Ni) content of not more than 5 ppm and a molybdenum (Mo) content of not more than 5 ppm. (10) The high purity polyphosphoric acid of (8) above, wherein the chromium (Cr) content is not more than 2 ppm, the nickel (Ni) content is not more than 2 ppm and the molybdenum (Mo) content is not more than 2 ppm.
Before explaining the present invention in detail, the indication of the phosphoric acid concentration is explained in the following.
In the present invention, phosphoric acid is a polycondensation product of orthophosphoric acid, and its concentration is generally expressed after orthophosphoric acid conversion or P,0s conversion. Phosphoric acid having an orthophosphoric acid concentration of 100% corresponds to phosphoric acid having a P,0s concentration of 72.4%, wherein the relationship between both concentrations is expressed by the following equation:
P,0s concentration (%) = orthophosphoric acid concentration (%) x 0.724
Phosphoric acid having a P,0s concentration of less than
72.4% is an aqueous phosphoric acid solution containing a : polycondensation product of orthophosphoric acid and water in an equilibrium state. Phosphoric acid having a P,0s concentration of not less than 72.4% consists solely of a polycondensation product of orthophosphoric acid and is called polyphosphoric acid, strong phosphoric acid or super phosphoric acid. In the present invention, any phosphoric acid concentration is expressed in P,05 concentration.
In a first embodiment of the method for purifying phosphoric acid according to the present invention, phosphoric acid containing arsenic is brought into contact with hydrogen halide alone and the arsenic is removed from the phosphoric acid.
The reason why an arsenic removal effect is expressed by this method is uncertain, but it is postulated that hydrogen halide causes arsenic in phosphoric acid to convert to an arsenic compound having a high volatility, such as arsenic halide and arsenic hydride, and the compound evaporates at a treatment temperature of the purification method of the present invention and is discharged from the system along with hydrogen halide.
It is also unknown as to the chemical state of arsenic in phosphoric acid, but the arsenic is considered to be in the state of arsenic acid, arsenious acid, diarsenic pentaoxide, diarsenic trioxide and the like.
While the phosphoric acid concentration applicable to the first embodiment is free of any particular limitation, when the method is applied to low concentration phosphoric acid, hydrogen halide is dissolved in water to enhance corrosion of phosphoric acid and to cause hydrogen halide to remain after treatment.
Thus, this method is advantageously applied to phosphoric acid having relatively lower water content (high phosphoric acid : concentration). Particularly, when it is applied to polyphosphoric acid, which is completely anhydrous, hydrogen halide does not remain in polyphosphoric acid, thus enabling elimination of corrosion. When the phosphoric acid to be used is polyphosphoric acid, a concentration range free of freezing
) point, namely, a P,0s concentration of 75-77% or not less than 80% is preferable. In consideration of handling property, the upper limit of P,0s concentration is preferably 90%. : In a second embodiment of the method for purifying phosphoric acid of the present invention, phosphoric acid containing arsenic is brought into contact with hydrogen halide in the presence of a compound capable of generating hydrogen halide under acidic conditions, and the arsenic is removed from the phosphoric acid. In this embodiment, arsenic can be removed highly efficiently. The compound capable of generating hydrogen ~ halide under acidic conditions may be an organic or inorganic compound. Particularly, it is preferably metal halide having a ‘reducing action, more preferably halide of iron(II), copper(I) or tin(II), most preferably chloride of these metals, particularly preferably chloride of iron(II) or tin(II).
When phosphoric acid containing arsenic is brought into contact with hydrogen halide in the presence of a compound capable of generating hydrogen halide under acidic conditions, the arsenic removal effect is promoted for unknown reasons, but : 20 it is postulated that arsenic itself becomes easily reducible and easily becomes a volatile arsenic compound, such as arsenic halide and arsenic hydride, which is easily evaporated at the treatment temperature of the purification method of the present invention, because the effect is particularly striking when metal halide acting as a reducing agent is added. : The compound capable of generating hydrogen halide under acidic conditions in the second embodiment is added in a trace amount, which is preferably less than 1 wt%, more preferably less than 0.5 wt%, of a weight of phosphoric acid. When it is used in a greater amount, an arsenic removal effect is assumed to be enhanced more. Particularly when this compound is metal halide, however, an impurity derived from a metal in the metal halide unpreferably remains. When the residual impurity is to be avoided, or when high purity phosphoric acid, particularly high purity polyphosphoric acid is desired, the first embodiment wherein phosphoric acid containing arsenic is brought into contact with hydrogen halide alone is preferable rather than the second embodiment.
In the first and the second embodiments, phosphoric acid is brought into contact with hydrogen halide in any typical gas- liquid mixing apparatus, which may be of a batch type or a continuous type. For example, a method wherein a batch reaction vessel is used and phosphoric acid is vigorously stirred with direct blowing of hydrogen halide therein, a method wherein a © 10 static mixer or ejector is used and phosphoric acid and hydrogen halide are continuously mixed, a method wherein the both methods are combined, and the like can be employed. The hydrogen halide : to be used in the present invention may be hydrogen chloride, hydrogen bromide and the like, with preference given to hydrogen chloride because it is obtained most easily and economically.
In the first and the second embodiments, the necessary amount of hydrogen halide relative to phosphoric acid depends greatly on the gas-liquid mixing efficiency of the apparatus used, and the range of the amount is difficult to specify.
Because arsenic in phosphoric acid is considered to be trivalent or pentavalent, at least not less than 3 to 5 molar equivalents of hydrogen halide relative to the arsenic content is considered to be necessary. In the case of the easiest method wherein a : batch reaction vessel is used and phosphoric acid is vigorously stirred with direct blowing of hydrogen halide therein, for example, hydrogen chloride is blown into 500 ml of polyphosphoric acid (P,0s concentration 85%) having an arsenic content of 50 ppm preferably at a rate of 1-100 ml/min, more preferably 10-80 ml/min, for preferably not less than 30 min, more preferably not less than 60 min.
In the first and the second embodiments, the treatment temperature varies depending on the phosphoric acid concentration and the material of the reactor, but may be any within the range of from about 50°C to 200°C. In consideration of the corrosion of a stainless material industrially used for a reactor and the like by phosphoric acid, it is desirably not more than 150°C. For promotion of evaporation of the generated arsenic compound, it is desirably at least 50°C, more preferably not less than 100°C. The pressure is free of any particular limitation and can be set optionally, wherein a sufficient dearsenic effect can be achieved under an atmospheric pressure. : In the first and the second embodiments, moreover, the arsenic compound is discharged from the system together with hydrogen halide. These compounds may be preferably absorbed by water and neutralized, or absorbed by an aqueous alkaline solution of sodium hydroxide, potassium hydroxide and the like.
According to the method for purifying phosphoric acid of the present invention, phosphoric acid having a low arsenic content of not more than about 1 ppm can be obtained by an easy method. Particularly, when the method is applied in the presence of a compound capable of generating hydrogen halide under acidic conditions, phosphoric acid having a low arsenic content of not more than about 0.1 ppm can be obtained.
Inasmuch as the method does not require an equipment cost for a filtration step or a deaeration step or the use of a sodium compound, such as sodium sulfide, sodium hydrosulfide and the like, unlike the conventional method, it does not happen that sodium remains in a large amount in phosphoric acid. By the application of the purification method of the present invention : 25 to phosphoric acid having low contents of heavy metal, sodium : and silica, which is obtained by the dry method, phosphoric acid having a low arsenic content and low contents of heavy metal, silica and sodium can be obtained.
The method for purifying phosphoric acid of the present invention does not require conventional filtration steps.
Therefore, the method is applicable to high concentration phosphoric acid, particularly polyphosphoric acid. By the application of the purification method of the present invention to polyphosphoric acid having low contents of heavy metal, silica and sodium but a high arsenic content, which is obtained
. by the dry method, high purity polyphosphoric acid having a low ’ arsenic content and low contents of heavy metal, silica and sodium, which has not been obtained heretofore, can be afforded.
To be specific, by the application of the purification © 5 method of the present invention to polyphosphoric acid prepared by adding phosphoric anhydride to industrial phosphoric acid and dissolving therein, polyphosphoric acid having an iron (Fe) content of not more than 20 ppm, a sodium (Na) content of not more than 100 ppm, a silica (Si0,) content of not more than 50 ppm, and an arsenic (As) content of not more than 1 ppm, and further, a chromium (Cr) content of not more than 5 ppm, a nickel (Ni) content of not more than 5 ppm, and a molybdenum (Mo) content of not more than 5 ppm can be obtained.
By the application of the purification method of the present invention to polyphosphoric acid prepared by adding phosphoric anhydride to phosphoric acid as a reagent or phosphoric acid as a food additive and dissolving therein, polyphosphoric acid having an iron (Fe) content of not more than ~ 10 ppm, a sodium (Na) content of not more than 5 ppm, a silica (Si0,) content of not more than 5 ppm, and an arsenic (As) content of not more than 1 ppm, and further, a chromium (Cr) content of not more than 2 ppm, a nickel (Ni) content of not more than 2 ppm, and a molybdenum (Mo) content of not more than 2 ppm can be obtained.
The content of each element of the polyphosphoric acid in the present invention was measured by the following methods.
Arsenic was measured according to JIS-K 0102 (1993).
Inasmuch as an organic substance is considered to be absent from a polyphosphoric acid sample, an organic substance decomposition step with sulfuric acid/nitric acid as described in the JIS was omitted. Iron, chromium, nickel, molybdenum and silica were quantitatively determined by an inductively coupled plasma (ICP) analysis. The ICP sample solution was prepared by adding hydrochloric acid to polyphosphoric acid to give 1.2 M hydrochloric acid solution. A calibration curve of the phosphoric acid solution was adjusted to achieve the same concentration as the sample solution. Sodium was quantitatively determined by atomic absorption spectrometry. The atomic absorption sample solution was the same as it was for ICP. The
P,0s concentration of polyphosphoric acid was determined by titration using 1 M sodium hydroxide solution.
The present invention is explained in more detail in the following by referring to Examples. The present invention is not limited by these examples.
Example 1
Commercially available polyphosphoric acid obtained by a dry method (500 ml, P,0s concentration 84.9%) having an arsenic content of 58 ppm was stirred with heating at 130°C, during which a glass tube having a glass bowl filter was inserted and hydrogen chloride gas was blown in at an aeration rate of 20 : ml/min for about 2 hours to give high purity polyphosphoric acid.
The discharged hydrogen chloride gas was trapped in an aqueous sodium hydroxide solution. The analysis results of the obtained high purity polyphosphoric acid are shown in Table 1.
Example 2
Commercially available polyphosphoric acid obtained by a dry method (500 ml, P,0s concentration 84.2%) having an arsenic content of 8 ppm was cast in a 1l(one) liter three-necked glass flask and stirred with heating at 150°C, during which a glass tube having a glass bowl filter was inserted and hydrogen chloride gas was blown in at an aeration rate of 50 ml/min for about 2 hours to give high purity polyphosphoric acid. The discharged hydrogen chloride gas was trapped in an aqueous sodium hydroxide solution. The analysis results of the obtained high purity polyphosphoric acid are shown in Table 1.
Example 3
Phosphoric anhydride (200 g) having an arsenic content of 25 ppm was added to phosphoric acid as a reagent (422 g, P,0s concentration 61.5%) having an arsenic content of 0.1 ppm. The mixture was stirred with heating at 120°C to give a homogeneous liquid, whereby polyphosphoric acid (P,0s concentration 84.0%) having an arsenic content of 8 ppm was prepared. While stirring under heating at 150°C, a glass tube with a glass bowl filter was inserted and hydrogen chloride gas was blown in at an aeration rate of 20 ml/min for about 3 hours to give high purity polyphosphoric acid. The discharged hydrogen chloride gas was trapped in an aqueous sodium hydroxide solution. The analysis results of the obtained high purity polyphosphoric acid are shown in Table 1.
Example 4
Phosphoric anhydride (170 g) having an arsenic content of 25 ppm was added to commercially available polyphosphoric acid obtained by a dry method (330 g, P,05 concentration 76.0%) having an arsenic content of 5 ppm. The mixture was stirred - 15 under heating at 120°C to give a homogeneous liquid, whereby polyphosphoric acid (P,0s concentration 84.2%) having an arsenic content of 11 ppm was prepared. While stirring under heating at 150°C, a glass tube with a glass bowl filter was inserted and hydrogen chloride gas was blown in at an aeration rate of 20 ml/min for about 3 hours to give high purity polyphosphoric acid.
The discharged hydrogen chloride gas was trapped in an aqueous sodium hydroxide solution. The analysis results of the obtained ~ high purity polyphosphoric acid are shown in Table 1.
Example 5
Industrial phosphoric acid (500 ml, P,0s concentration 65%) having an arsenic content of 15 ppm was cast in a 1(one) liter three-necked glass flask and stirred with heating at 130°C, during which a glass tube having a glass bowl filter was inserted and hydrogen chloride gas was blown in at an aeration rate of 50 ml/min. The discharged hydrogen chloride gas was trapped in an aqueous sodium hydroxide solution. As a result, the concentration of arsenic in phosphoric acid at 180 minutes after the start of blowing was 0.8 ppm.
Example 6 :
The same treatment as in Example 5 was applied except that iron chloride(II) (0.1 g) was added before blowing in hydrogen chloride. As a result, the concentration of arsenic in phosphoric acid at 120 minutes after the start of blowing was 0.07 ppm.
Example 7
The same treatment as in Example 5 was applied except that tin chloride(II) dihydrate (0.5 g) was added before blowing in hydrogen chloride. As a result, the concentration of arsenic ‘in phosphoric acid at 120 minutes after the start of blowing was 0.08 ppm.
The analysis results of each element contained in the high purity polyphosphoric acids obtained in Examples 1-4 are shown in Table 1. For comparison, the analysis results of commercially available product A, which is polyphosphoric acid obtained by a dry method, and commercially available product B, which is polyphosphoric acid obtained by a wet method, are also shown in Table 1.
Table 1 : Analysis |Example [Example [Example [Example | Commer- Commer- item 1 2 3 4 cially | cially available |available product A |product B centra- 84.9 84.2 84.0 84.2 85.0 84.3 tion (%)
Fe cr content 0.1 0.1 0.7 6.3
Ni content 0.3 0.1
Mo )
Na content 0.1 0.1 0.1 0.1 0.2 250
Co sio, : lcontent | <> = 1 = : = — = 20
AS
In Table 1, respective contents are in the unit of ppm.
As is evident from Table 1, the commercially available product A (polyphosphoric acid obtained by a dry method) showed low contents of heavy metal, silica and sodium but a high arsenic content, and the commercially available product B (polyphosphoric acid obtained by a wet method) showed a low arsenic content but high contents of heavy metal, sodium and silica. In contrast, the high purity polyphosphoric acids of
Examples 1-4 showed low arsenic contents, and low contents of heavy metal, sodium and silica. From Examples 6 and 7, it is evident that, when phosphoric acid containing arsenic is brought into contact with hydrogen halide in the presence of a compound capable of generating hydrogen halide under acidic conditions, such as iron chloride(II), tin chloride(II) and the like, an effect of removing arsenic in phosphoric acid can be enhanced.
As is evident from the following explanation, the method for purifying phosphoric acid of the present invention can effectively remove arsenic in phosphoric acid, which is harmful for human being, by a simple manipulation wherein phosphoric acid is brought into contact with hydrogen halide. To be : specific, the arsenic content of several dozen ppm of general industrial phosphoric acid can be reduced to not more than about 1 ppm. When the above-mentioned step is applied in the presence of a compound capable of generating hydrogen halide under acidic conditions, the removal to the level of not more than about 0.1 ppm is possible.
This method includes a simple treatment step and requires no special apparatus. As a result, the total cost for the treatment is low, and since a sodium compound is not used, unlike the conventional method, sodium does not remain in a large amount in phosphoric acid.
Moreover, since the method for purifying phosphoric acid of the present invention does not require a filtration step, unlike a conventional purification method, it can be applied to high concentration phosphoric acid, particularly polyphosphoric
. acid. Particularly, when polyphosphoric acid obtained by a dry method and having low contents of heavy metal, sodium and silica but a high arsenic content is subjected to the purification method of the present invention, high purity polyphosphoric acid having a low arsenic content and low contents of heavy metal, silica and sodium can be afforded, which has not been obtained heretofore. Such high purity polyphosphoric acid is highly safe and can reduce the environmental burden. Therefore, it is applicable to a broader range of use in the fields of food, medicaments and electronic materials.
This application is based on patent application Nos. 373696/1998 and 230628/1999 filed in Japan, the contents of which are hereby incorporated by reference.
Claims (10)
1. A method for purifying phosphoric acid, which comprises bringing phosphoric acid containing arsenic into contact with hydrogen halide, thereby to remove the arsenic from the phosphoric acid.
2. The purification method of claim 1, wherein the phosphoric acid containing the arsenic is brought into contact with hydrogen halide in the presence of a compound capable of generating hydrogen halide under acidic conditions.
3. The purification method of claim 2, wherein the compound capable of generating hydrogen halide under acidic conditions is added in a proportion of less than 1 wt% of a weight of the phosphoric acid.
4. The purification method of claim 2, wherein the compound capable of generating hydrogen halide under acidic conditions is a chloride of iron(II), copper(I) or tin(II). : 20
5. The purification method of claim 1, wherein the hydrogen halide is hydrogen chloride.
6.: The purification method of claim 1, wherein the phosphoric acid has a P,0s concentration of not less than 72.4%.
7. A high purity polyphosphoric acid having an iron (Fe) content of not more than 20 ppm, a sodium (Na) content of not more than 100 ppm, a silica (SiO,) content of not more than 50 ppm and an arsenic (As) content of not more than 1 ppm.
8. The high purity polyphosphoric acid of claim 7, wherein the iron (Fe) content is not more than 10 ppm, the sodium (Na) : content is not more than 5 ppm, the silica (SiO,) content is not more than 5 ppm and the arsenic (As) content is not more than 1
EJ = p
. . ppm.
9. The high purity polyphosphoric acid of claim 7, which has a chromium (Cr) content of not more than 5 ppm, a nickel (Ni) content of not more than 5 ppm and a molybdenum (Mo) content of not more than 5 ppm.
10. The high purity polyphosphoric acid of claim 8, wherein the chromium (Cr) content is not more than 2 ppm, the nickel (Ni). content is not more than 2 ppm and the molybdenum (Mo) content is not more than 2 ppm.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP37369698 | 1998-12-28 |
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| Publication Number | Publication Date |
|---|---|
| ZA200106211B true ZA200106211B (en) | 2002-07-29 |
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| ZA200106211A ZA200106211B (en) | 1998-12-28 | 2001-07-27 | Method for purification of phosphoric acid and high purity polyphosphoric acid. |
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| JPS5297394A (en) * | 1976-02-13 | 1977-08-16 | Toyo Soda Mfg Co Ltd | Removal of organic matter in phosphoric acid |
| IT1251686B (en) * | 1991-10-11 | 1995-05-19 | Agrimont Spa | PROCESS FOR THE REMOVAL OF CADMIUM FROM PHOSPHORIC ACID SOLUTIONS. |
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