US3414376A - Corrosion inhibitor for phosphoric acid - Google Patents
Corrosion inhibitor for phosphoric acid Download PDFInfo
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- US3414376A US3414376A US537751A US53775166A US3414376A US 3414376 A US3414376 A US 3414376A US 537751 A US537751 A US 537751A US 53775166 A US53775166 A US 53775166A US 3414376 A US3414376 A US 3414376A
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- Prior art keywords
- iodide
- phosphoric acid
- acid
- weight percent
- corrosion
- Prior art date
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- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 title description 72
- 229910000147 aluminium phosphate Inorganic materials 0.000 title description 36
- 238000005260 corrosion Methods 0.000 title description 19
- 230000007797 corrosion Effects 0.000 title description 19
- 239000003112 inhibitor Substances 0.000 title description 9
- 235000011007 phosphoric acid Nutrition 0.000 description 36
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 34
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 27
- 239000002253 acid Substances 0.000 description 22
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 21
- 238000000034 method Methods 0.000 description 19
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 16
- 239000000654 additive Substances 0.000 description 12
- 235000009518 sodium iodide Nutrition 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 229910000831 Steel Inorganic materials 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 150000004694 iodide salts Chemical class 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- UAYWVJHJZHQCIE-UHFFFAOYSA-L zinc iodide Chemical compound I[Zn]I UAYWVJHJZHQCIE-UHFFFAOYSA-L 0.000 description 4
- XZXYQEHISUMZAT-UHFFFAOYSA-N 2-[(2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound CC1=CC=C(O)C(CC=2C(=CC=C(C)C=2)O)=C1 XZXYQEHISUMZAT-UHFFFAOYSA-N 0.000 description 3
- 229940107816 ammonium iodide Drugs 0.000 description 3
- 229910000043 hydrogen iodide Inorganic materials 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 230000000670 limiting effect Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- UNMYWSMUMWPJLR-UHFFFAOYSA-L Calcium iodide Chemical compound [Ca+2].[I-].[I-] UNMYWSMUMWPJLR-UHFFFAOYSA-L 0.000 description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 2
- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 229940046413 calcium iodide Drugs 0.000 description 2
- 229910001640 calcium iodide Inorganic materials 0.000 description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 2
- 229940006461 iodide ion Drugs 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229960003671 mercuric iodide Drugs 0.000 description 2
- YFDLHELOZYVNJE-UHFFFAOYSA-L mercury diiodide Chemical compound I[Hg]I YFDLHELOZYVNJE-UHFFFAOYSA-L 0.000 description 2
- 238000000247 postprecipitation Methods 0.000 description 2
- 229910001414 potassium ion Inorganic materials 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000011253 protective coating Substances 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- RXMRGBVLCSYIBO-UHFFFAOYSA-M tetramethylazanium;iodide Chemical compound [I-].C[N+](C)(C)C RXMRGBVLCSYIBO-UHFFFAOYSA-M 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- 241000501754 Astronotus ocellatus Species 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- -1 ferrous metals Chemical class 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000003930 superacid Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/04—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in markedly acid liquids
Definitions
- This invention relates to inhibiting corrosion by phosphoric acid in contact with ferrous materials.
- the invention relates to a method for inhibiting corrosion by phosphoric acid comprising adding to the phosphoric acid a soluble ionizable iodide and sulfuric acid.
- the invention relates to an inhibited phosphoric acid composition comprising phosphoric acid with minor amounts of added sulfuric acid and a soluble ionizable iodide.
- Another object of this invention is to provide an improved corrosion inhibitor for phosphoric acid. Another object of the invention is to provide a phosphoric acid composition of reduced corrosivity.
- FIGURES 1 and 2 represent the effect of various additives on the corrosion rate of phosphoric acid in contact with mild steel.
- the phosphoric acid which is treated according to my invention can be that produced by various processes, and can be of a wide range of concentration.
- suitable types of phosphoric acid are the so-called furnace process acid and the so-called wet-process acid.
- suitable concentrations of acid for treatment according to my process are filter acid, which usually analyzes in the neighborhood of 30-35 weight percent P 0 merchant acid, which usually analyzes in the neighborhood of 50-55 weight percent P 0 and super acid, which usually analyzes 68 weight percent P 0 or more. Because of the nature of the impurities present, wet-process acid presents the most trouble in shipping, and also comprises the large bulk of the phosphoric acid production today. My invention is especially useful in treating wet-process phosphoric acid.
- the additives of this invention can be incorporated into the acid at any suitable point during the process of its manufacture. They are especially advantageously added to the newly-produced merchant acid just prior to or during its introduction into the acid storage tanks.
- the sulfuric acid additive can be of any concentration, but a highly concentrated sulfuric acid is preferred simply to reduce the dilution of the phosphoric acid product. Oleum is also suitable for this use.
- the amount of sulfuric acid to be added can vary over a wide range, but preferably will be between about 2 and about 35, more preferably between about 5 and about 35 weight percent based on the phosphoric acid.
- the soluble ionizable iodide additive can be any iodide which dissolves and ionizes, in the acid being treated, sufficiently to provide at least about 50 p.p.m. iodide ion.
- iodide ion iodide which dissolves and ionizes, in the acid being treated, sufficiently to provide at least about 50 p.p.m. iodide ion.
- hydrogen iodide sodium iodide
- ammonium iodide or mixtures of these.
- suitable soluble ionizable iodides include tetramethyl ammonium iodide, zinc iodide, and calcium iodide.
- potassium iodide has an excellent inhibiting effect when used in conjunction with sulfuric acid, the potassium ion causes a voluminous precipitation of sludge from wet-process acid. This may be desirable in some instances where it is desirable to remove this sludge and reduce post-precipitation, but other sources of potassium ion than the iodide are cheaper, and for this reason the potassium iodide is presently less preferred.
- the soluble ionizable iodide should be added in amount suflicient to obtain the synergistic reduction in corrosivity in conjunction with the sulfuric acid, which is usually a mini- 'mum of at least about 50 p.p.m. based on the weight of the phosphoric acid. Addition of more than about 2 weight percent serves little purpose, since additional amounts often seem to be decomposed or in some other manner rendered ineffective.
- ferrous alloys in general can be used to store phosphoric acid when treated according to this invention.
- a 76% phosphoric acid can be treated by this invention to have a corrosion rate of 1020 mild steel at F. of 2.5 m.p.y. (milli-inches per year) Or even less.
- FIGURE 1 illustrates the effect of sodium iodide alone, but it should be mentioned that severe pitting was observed on these coupons. Whenever pitting occurs, the practical elfect on, e.g., a steel pipe or vessel is worse than indicated by weight loss alone.
- the upper curve of FIGURE 2 illustrates the effect of sulfuric acid alone.
- the lower curve of FIGURE 2 illustrates the effect of the combined additives.
- the points on the lower curve were obtained by mixing 50, 200, 400 and 400 parts per million iodide by weight, as sodium iodide, to 5, 10, 22 and 35 weight percent sulfuric acid by weight, respectively, all based on the phosphoric acid weight.
- Corrosion rates were determined on 1020 mild steel coupons at 120 F., in a manner similar to Example 1, in 76% wet-process phosphoric acid with no additives and with 200 p.p.m. of various iodides, using no added sulfuric acid. Corrosion rates in m.p.y. were as follows: no iodide, 1910; KI, 151; Neil, 153; NH I, 154; and HI, 153.
- Corrosion rates were determined on 1020 mild steel coupons at 120 F., in a manner similar to Example I, in 76% wet-process phosphoric acid to which was added percent concentrated sulfuric acid and 200 p.p.m. of various soluble ionizable iodides. Corrosion rates in m.p.y. were as follows: no iodide, 59; sodium iodide, 10; tetramethyl ammonium iodide, zinc iodide, 21; mercuric iodide, 63; and calcium iodide, 10. Mercuric iodide, which is virtually insoluble, had no beneficial effect.
- the method of reducing corrosivity of merchant grade wet process phosphoric acid toward ferrous metal which comprises adding thereto at least about p.p.m. of a soluble ioniza-ble iodide and from about 2 to about 35 weight percent of sulfuric acid based on said phosphoric acid.
- said iodide is selected from the group consisting of sodium iodide, potassium iodide, ammonium iodide and hydrogen iodide.
- composition of claim 4 wherein said iodide is selected from the group consisting of sodium iodide, potassium iodide, ammonium iodide and hydrogen iodide.
- composition of claim -5 wherein said iodide is present in an amount between about 50 ppm. and about 2 weight percent, and said sulfuric acid is present in an amount between about 5 and about 35 weight percent.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Description
Dec. 3, 1968 w. P. BANKS CORROSION INHIBITOR FOR PHOSPHORIC ACID 2 Sheets-Sheet 1 Filed March 28. 1966 CORROSION RATE ON 1020 MILD STEEL AT |20 F 76 WET PROCESS PHOSPHORIC ACID WITH ADDED SODIUM IODIDE O O O O 2 m m mwm mmxozTIdE mham 2059200 mm zm 05G] 0.030 0040 Y WEIGHT PERCENT ADDED IODIDE (AS IODIDE ION) as U m m w w m a L m A TTOR/VEY LIQUID PHASE CORROSION RATE, MlLLl-INCHES PER YEAR Dec. 3, 1968 w. P. BANKS 3,414,376
CORROSION INHIBITOR FOR PHOSPHORIC ACID Filed March 28. 1966 2 Sheets-Sheet 2 AT I20 F IC ACID ACID PLUS SODIUM IODIDE WEIGHT PERCENT ADDITIVE 2 INVENTOR.
WILLIAM R BANKS id-2211M (Z, 4 gv 4 ATTORNE United States Patent 3 414,376 CORROSION INHIBITOR FOR PHOSPHORIC ACID William P. Banks, Ponca City, Okla, assignor t0 Continental Oil Company, Ponca City, Okla., a corporation of Delaware Filed Mar. 28, 1966, Ser. No. 537,751 6 Claims. (Cl. 23165) ABSTRACT OF THE DISCLOSURE Corrosivity of merchant grade wet process phosphoric acid toward ferrous metals is greatly reduced by addition of at least about 50 ppm. iodide ion and about 2-35 weight percent sulfuric acid.
This invention relates to inhibiting corrosion by phosphoric acid in contact with ferrous materials. In one aspect, the invention relates to a method for inhibiting corrosion by phosphoric acid comprising adding to the phosphoric acid a soluble ionizable iodide and sulfuric acid. In another aspect, the invention relates to an inhibited phosphoric acid composition comprising phosphoric acid with minor amounts of added sulfuric acid and a soluble ionizable iodide.
One of the handicaps which has resisted the widespread use of phosphoric acid is the difficulty of Shipping this material in ferrous containers. While it is possible to employ glass carboys to hold phosphoric acid, it has not been possible heretofore to ship strong phosphoric acids in iron and steel shipping containers, nor to store such acid in other than chemically resistant and consequently expensive materials.
It has been proposed to prevent the corrosion and dissolution of steel or iron drums or containers used for the storage and transportation of phosphoric acid by dissolving in the acid a material capable of precipitating a protective coating on the steel. This precipitation may be accomplished in the presence or absence of an acid regulator. The precipitated protective coating is usually a metal below iron and above mercury in the electromotive series, such as arsenic, while the acid regulator is usually an organic substance such as pyridine bases, crude anthracene, sulfite, lye, resins, wash acids from refining hydrocarbons, etc., many of which are highly colored. In previous proposals it has been necessary to decolorize the inhibited acid, in order to obtain a water-white product. By this means appreciable amounts of the inhibitor were removed from the acid.
Other inhibitors for phosphoric acid have been proposed in the art. For instance, US. Patent 1,809,041 discloses the use of various iodides, and US. Patent 3,119,662 discloses the use of sulfuric acid as a corrosion inhibitor for phosphoric acid. However, these various inhibitors have not been as effective as might be desired.
Accordingly, it is an object of this invention to provide an improved corrosion inhibitor for phosphoric acid. Another object of the invention is to provide a phosphoric acid composition of reduced corrosivity.
Other aspects, objects and the various advantages of this invention will be gained from study of this specification, the claims, and the drawing, in which:
FIGURES 1 and 2 represent the effect of various additives on the corrosion rate of phosphoric acid in contact with mild steel.
I have discovered that addition of a soluble ionizable iodide and sulfuric acid to phosphoric acid results in an acid of much lower corrosivity than when equivalent amounts of either additive are used alone. I have further found that when, according to a presently-preferred em- 3,414,376 Patented Dec. 3, 1968 bodiment of my invention, the soluble ionizable iodide is one other than potassium iodide, the common phenomenon of post-precipitation in wet-process phosphoric acid is substantially reduced.
The phosphoric acid which is treated according to my invention can be that produced by various processes, and can be of a wide range of concentration. Illustrative but not limiting of suitable types of phosphoric acid are the so-called furnace process acid and the so-called wet-process acid. Illustrative but not limiting of suitable concentrations of acid for treatment according to my process are filter acid, which usually analyzes in the neighborhood of 30-35 weight percent P 0 merchant acid, which usually analyzes in the neighborhood of 50-55 weight percent P 0 and super acid, which usually analyzes 68 weight percent P 0 or more. Because of the nature of the impurities present, wet-process acid presents the most trouble in shipping, and also comprises the large bulk of the phosphoric acid production today. My invention is especially useful in treating wet-process phosphoric acid.
The additives of this invention can be incorporated into the acid at any suitable point during the process of its manufacture. They are especially advantageously added to the newly-produced merchant acid just prior to or during its introduction into the acid storage tanks.
The sulfuric acid additive can be of any concentration, but a highly concentrated sulfuric acid is preferred simply to reduce the dilution of the phosphoric acid product. Oleum is also suitable for this use. The amount of sulfuric acid to be added can vary over a wide range, but preferably will be between about 2 and about 35, more preferably between about 5 and about 35 weight percent based on the phosphoric acid.
The soluble ionizable iodide additive can be any iodide which dissolves and ionizes, in the acid being treated, sufficiently to provide at least about 50 p.p.m. iodide ion. Presently preferred are hydrogen iodide, sodium iodide, ammonium iodide, or mixtures of these. Other examples of suitable soluble ionizable iodides include tetramethyl ammonium iodide, zinc iodide, and calcium iodide. It has been discovered that, although potassium iodide has an excellent inhibiting effect when used in conjunction with sulfuric acid, the potassium ion causes a voluminous precipitation of sludge from wet-process acid. This may be desirable in some instances where it is desirable to remove this sludge and reduce post-precipitation, but other sources of potassium ion than the iodide are cheaper, and for this reason the potassium iodide is presently less preferred. The soluble ionizable iodide should be added in amount suflicient to obtain the synergistic reduction in corrosivity in conjunction with the sulfuric acid, which is usually a mini- 'mum of at least about 50 p.p.m. based on the weight of the phosphoric acid. Addition of more than about 2 weight percent serves little purpose, since additional amounts often seem to be decomposed or in some other manner rendered ineffective.
The corrosion-inhibiting effect of these additives is sufficient that ferrous alloys in general can be used to store phosphoric acid when treated according to this invention. For instance, a 76% phosphoric acid can be treated by this invention to have a corrosion rate of 1020 mild steel at F. of 2.5 m.p.y. (milli-inches per year) Or even less.
Further understanding of this invention will be gained by study of the following example, which is intended to be illustrative and not limiting.
EXAMPLE I Coupons of 1020 mild steel were prepared and immersed in 76% wet-process phosphoric acid alone, and in admixture with varying amounts of sodium iodide, 96.5% sulfuric acid, and mixtures of the two inhibitors. Corrosion rates were determined by weight loss of the cou- 3 pons after a measured time interval. All samples were held at 120 F. during the tests. FIGURE 1 illustrates the effect of sodium iodide alone, but it should be mentioned that severe pitting was observed on these coupons. Whenever pitting occurs, the practical elfect on, e.g., a steel pipe or vessel is worse than indicated by weight loss alone. The upper curve of FIGURE 2 illustrates the effect of sulfuric acid alone. The lower curve of FIGURE 2 illustrates the effect of the combined additives. The points on the lower curve were obtained by mixing 50, 200, 400 and 400 parts per million iodide by weight, as sodium iodide, to 5, 10, 22 and 35 weight percent sulfuric acid by weight, respectively, all based on the phosphoric acid weight. One point, not shown, comprised 35 weight percent of each additive, and the resulting corrosion rate was 17 m.p.y.
EXAMPLE II Corrosion rates were determined on 1020 mild steel coupons at 120 F., in a manner similar to Example 1, in 76% wet-process phosphoric acid with no additives and with 200 p.p.m. of various iodides, using no added sulfuric acid. Corrosion rates in m.p.y. were as follows: no iodide, 1910; KI, 151; Neil, 153; NH I, 154; and HI, 153.
EXAMPLE III Corrosion rates were determined on 1020 mild steel coupons at 120 F., in a manner similar to Example I, in 76% wet-process phosphoric acid to which was added percent concentrated sulfuric acid and 200 p.p.m. of various soluble ionizable iodides. Corrosion rates in m.p.y. were as follows: no iodide, 59; sodium iodide, 10; tetramethyl ammonium iodide, zinc iodide, 21; mercuric iodide, 63; and calcium iodide, 10. Mercuric iodide, which is virtually insoluble, had no beneficial effect.
From the preceding examples, it can be seen that the combined additives result in a substantially lower rate of corrosion than when an equivalent amount of either additive is used alone.
Having thus described the invention by providing specific examples thereof, it is to be understood that no undue limitations or restrictions are to be drawn by reason thereof and that many variations and modifications are within the scope of the invention.
What is claimed is:
1. The method of reducing corrosivity of merchant grade wet process phosphoric acid toward ferrous metal which comprises adding thereto at least about p.p.m. of a soluble ioniza-ble iodide and from about 2 to about 35 weight percent of sulfuric acid based on said phosphoric acid.
2. The method of claim 1 wherein said iodide is selected from the group consisting of sodium iodide, potassium iodide, ammonium iodide and hydrogen iodide.
3. The method of claim 2 wherein said iodide is added in an amount between about 50 p.p.m. and about 2 weight percent, and said sulfuric acid is added in an amount between about 5 and about 35 weight percent based on said phosphoric acid.
4. Merchant grade wet process phosphoric acid of reduced corrosivity toward ferrous metals comprising said acid containing at least about 50 p.p.m. of a soluble ionizable iodide and from about 2 to about 35 weight percent of sulfuric acid based on said phosphoric acid.
5. The composition of claim 4 wherein said iodide is selected from the group consisting of sodium iodide, potassium iodide, ammonium iodide and hydrogen iodide.
6. The composition of claim -5 wherein said iodide is present in an amount between about 50 ppm. and about 2 weight percent, and said sulfuric acid is present in an amount between about 5 and about 35 weight percent.
References Cited UNITED STATES PATENTS 1,809,041 6/1931 Jenkins et a1. 23-165 2,567,156 9/1951 Malowan 23-165 3,044,854 7/1962 Young 23-165 3,119,662 1/1964 Viventi et al. 23-165 1,951,077 3/1934 Woodstock 23-165 OSCAR R. VERTIZ, Primary Examiner.
A. I. GREIF, Assistant Examiner.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US537751A US3414376A (en) | 1966-03-28 | 1966-03-28 | Corrosion inhibitor for phosphoric acid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US537751A US3414376A (en) | 1966-03-28 | 1966-03-28 | Corrosion inhibitor for phosphoric acid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3414376A true US3414376A (en) | 1968-12-03 |
Family
ID=24143955
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US537751A Expired - Lifetime US3414376A (en) | 1966-03-28 | 1966-03-28 | Corrosion inhibitor for phosphoric acid |
Country Status (1)
| Country | Link |
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| US (1) | US3414376A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4228140A (en) * | 1977-06-13 | 1980-10-14 | The Nash Engineering Company | Production of phosphates |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1809041A (en) * | 1930-02-03 | 1931-06-09 | Swann Res Inc | Inhibitor |
| US1951077A (en) * | 1933-05-04 | 1934-03-13 | Victor Chemical Works | Purification of phosphoric acid |
| US2567156A (en) * | 1947-12-31 | 1951-09-04 | Monsanto Chemicals | Corrosion inhibitor for concentrated phosphoric acid |
| US3044854A (en) * | 1960-01-11 | 1962-07-17 | Collier Carbon & Chemical Co | Phosphoric acid |
| US3119662A (en) * | 1961-09-01 | 1964-01-28 | Nat Distillers Chem Corp | Stabilization of phosphoric acid |
-
1966
- 1966-03-28 US US537751A patent/US3414376A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1809041A (en) * | 1930-02-03 | 1931-06-09 | Swann Res Inc | Inhibitor |
| US1951077A (en) * | 1933-05-04 | 1934-03-13 | Victor Chemical Works | Purification of phosphoric acid |
| US2567156A (en) * | 1947-12-31 | 1951-09-04 | Monsanto Chemicals | Corrosion inhibitor for concentrated phosphoric acid |
| US3044854A (en) * | 1960-01-11 | 1962-07-17 | Collier Carbon & Chemical Co | Phosphoric acid |
| US3119662A (en) * | 1961-09-01 | 1964-01-28 | Nat Distillers Chem Corp | Stabilization of phosphoric acid |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4228140A (en) * | 1977-06-13 | 1980-10-14 | The Nash Engineering Company | Production of phosphates |
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