US20010022947A1

US20010022947A1 - Corrosion inhibition method suitable for use in potable water

Info

Publication number: US20010022947A1
Application number: US09/740,190
Authority: US
Inventors: Olen Riggs
Original assignee: A S Inc
Current assignee: GUARD PRODUCTS,LLC
Priority date: 1998-12-31
Filing date: 2000-12-19
Publication date: 2001-09-20
Anticipated expiration: 2019-07-26
Also published as: JP2004516387A; WO2002049966A3; CA2431455A1; WO2002049966A2; US6416712B2; AU2002231096A1; EP1343922A2

Abstract

Effective corrosion inhibitors having minimal organic content, particularly suitable for use in municipal drinking water systems, are described. The corrosion inhibiting additive is a stannous salt of a non-carbon acid.

Description

This application is a continuation-in-part of allowed U.S. application Ser. No. 09/360,768, filed Jul. 26, 1999, which claims priority to U.S. provisional application Ser. No. 60/114,551, filed Dec. 31, 1998, now abandoned, both of which are hereby incorporated by reference in their entirety.[0001]

FIELD OF THE INVENTION

The present invention relates to methods for inhibiting corrosion of corrodible metals present in contact with water in distributive water systems, particularly those associated with distribution of drinking water.

BACKGROUND OF THE INVENTION

In 1992, the United States Environmental Protection Agency adopted a standard for lead and copper in municipal drinking water. The standard sets action levels for lead and copper in standing samples collected from faucets with the highest risk for elevated lead and copper levels. The action level for lead is 15 μg/liter of water; the action level for copper is 1.3 mg/liter of water. The source of these and other metals in drinking water is primarily corrosion of plumbing system components, which include copper and lead-based solder as well as carbon steel and brass. Current anticorrosion additives, which include phosphate salts and/or zinc salts, have been in use for many years, but do not always provide adequate protection. There remains a need for improved corrosion inhibitors which are not themselves likely to present a health hazard when added to water.

Co-owned U.S. Pat. No. 5,202,028 and No. 5,510,057 describe the use of stannous salts, such as stannous octanoate or stannous chloride, typically in combination with other additives, in an alcoholic solvent medium, for reducing metal corrosion in, for example, cooling water tower systems. Additional solubilizing agents were also generally used. However, these additional components, including the alcoholic solvent, would be undesirable or even prohibited for use in drinking water supplies. Alcoholic solvents can provide a food source for the growth of bacteria and thus impact the sterility of drinking water supplies. Reduction in microbial growth would be beneficial in industrial water supplies as well. Accordingly, there is a need for effective corrosion inhibitors which minimize organic content.

SUMMARY OF THE INVENTION

The present invention includes, in one aspect, a method for inhibiting corrosion of corrodible metal in contact with water in a distributive water system. According to the method, a composition consisting essentially of a stannous (Sn ⁺²) salt of a non-carbon acid, or an aqueous solution thereof, is added to the water, and a concentration of the stannous salt corresponding to a tin level of about 0.01 to about 75 ppm, preferably about 0.05 to 25 ppm, is maintained in the water system.

The salt is preferably selected from stannous bromide, chloride, sulfate, nitrate, oxide, pyrophosphate, perchlorate, tetrafluoroborate, monofluorophosphate, ammonium fluoride, sodium fluoride, and fluorosilicate. Preferred salts include stannous bromide, chloride, sulfate, nitrate, and oxide. The stannous salt is preferably added in the form of an aqueous solution.

The corrodible metal is typically a ferrous metal, a brass metal, a copper-containing metal, or a lead-containing metal. In a preferred embodiment of the method, the distributive water system is a municipal drinking water system. Such a system may initially contain an alkali metal phosphate, such as a pyrophosphate, an orthophosphate, a hexametaphosphate, a hypophosphate, a polyphosphate, or a combination thereof, typically in an amount effective to provide a concentration of about 0.01 ppm to about 5 ppm of the alkali metal phosphate in the water system. The water system may also be treated to contain at least one component selected from a dispersing agent, a chelating agent, and a biocide.

In another aspect, the invention provides a related method for inhibiting corrosion of corrodible metal in contact with water in a distributive water system. In this method, a composition consisting essentially of a stannous (Sn ⁺²) salt of a non-carbon acid, or an aqueous solution thereof, is added to the water system, in combination with an alkali metal phosphate selected from a pyrophosphate, an orthophosphate, a hexametaphosphate, a hypophosphate, and a polyphosphate. A concentration of the stannous halide corresponding to a tin level of about 0.01 to about 75 ppm is maintained in the water system. Again, the salt is preferably selected from stannous bromide, chloride, sulfate, nitrate, oxide, pyrophosphate, perchlorate, tetrafluoroborate, monofluorophosphate, ammonium fluoride, sodium fluoride, and fluorosilicate, and more preferably selected from stannous bromide, chloride, sulfate, nitrate, and oxide. The alkali metal phosphate, e.g. sodium hexametaphosphate or sodium orthophosphate, is typically present in an amount effective to provide a concentration of about 0.01 ppm to about 5 ppm in the water system.

In a further aspect, the invention provides a metal corrosion inhibiting composition, consisting essentially of (i) a stannous salt of a non-carbon acid, or an aqueous solution thereof, and (ii) an alkali metal phosphate selected from a pyrophosphate, an orthophosphate, a hexametaphosphate, a hypophosphate, and a polyphosphate. In preferred embodiments, the stannous salt is selected from stannous bromide, chloride, sulfate, nitrate, oxide, pyrophosphate, perchlorate, tetrafluoroborate, monofluorophosphate, ammonium fluoride, sodium fluoride, and fluorosilicate, and more preferably from stannous bromide, chloride, sulfate, nitrate, and oxide. The stannous salt and alkali metal phosphate are present in relative amounts effective to produce concentrations of about 0.01 to about 75 ppm tin and about 0.01 ppm to about 5 ppm alkali metal phosphate, respectively, in a distributive water system.

The composition may also include one or more substances typically added to a distributive water stream for purposes other than inhibition of corrosion, such as a dispersing agent, chelating agent, or biocide. In one embodiment, the composition includes an acrylate copolymer, e.g. an acrylate/sulfonate copolymer.

These and other objects and features of the invention will become more fully apparent when the following detailed description of the invention is read in conjunction with the accompanying drawings.

DETAILED DESCRIPTION OF THE INVENTION

I. Definitions [0012]
“Corrosion” of a metal in contact with water, as used herein, refers to degradation of the metal due to chemical reaction with its environment, in this case, water and substances present in the water, including air. Such corrosion ultimately leads to dissolution or dispersion of the metal or metal compound in the water, observed as a loss of mass of the metal. [0013]
A “non-carbon” acid is an acid containing no carbon atoms, e.g. hydrochloric, sulfuric, phosphoric, or nitric acid. [0014]
As used herein, an “aqueous solution” of a stannous salt of a non-carbon acid refers to a composition of the salt in water, preferably in fairly high concentration, i.e., about 30 weight percent or greater, if the salt is of sufficient solubility in water to achieve this concentration. The composition may include an acid, e.g. HCl, H[0015] ₂SO₄, or HNO₃, to promote dissolution of the stannous salt. There are no other components in any appreciable concentration.
A “composition consisting essentially of” a stannous salt of a non-carbon acid (or aqueous solution) refers to the stannous salt, or aqueous solution, in combination with one or more optional components which do not materially affect the metal corrosion inhibiting characteristic(s) of the composition. Such components would typically be substances added to a distributive water stream for purposes other than inhibition of corrosion, as defined above. For example, dispersing or chelating agents, such as soluble anionic polymers (e.g. polyacrylates or acrylate copolymers), may be employed to reduce scale formation on solid surfaces; biocides may be added to reduce microbial growth. [0016]
A similar definition applies to compositions “consisting essentially of” a stannous salt of a non-carbon acid (or aqueous solution) and an alkali metal phosphate. Such compositions may also include components present for purposes other than inhibition of corrosion. [0017]

A “concentration of stannous salt which corresponds to a concentration of tin” in a given concentration range is determined from the relative molecular weights of the components, for example:



0.010	ppm tin corresponds to approx.	0.018	ppm SnSO₄,	0.016	ppm SnCl₂, or	0.023	ppm SnBr₂;
0.150	″	0.27	″	0.24	″	0.35	″
1.0	″	1.81	″	1.60	″	2.34	″
10	″	18.1	″	16.0	″	23.4	″
75	″	136	″	120	″	176	″

In the appended claims, water contained in a distributive water system to which a corrosion inhibitor is added is referred to as the “water system”, rather than simply “water”, to avoid confusion with the concentrated aqueous stannous halide solutions. [0019]
II. Preparation of Aqueous Stannous Salt Solutions and Use in Corrosion Inhibition [0020]
To form the minimal organic content corrosion inhibitors of the invention, any stannous salt of a non-carbon acid having sufficient aqueous solubility to be maintained in a water system at a concentration corresponding to a selected tin level in the range of about 0.01 to about 75 ppm may be used. As noted above, preferred salts include stannous bromide, chloride, sulfate, nitrate, oxide, pyrophosphate, perchlorate, tetrafluoroborate, monofluorophosphate, ammonium fluoride, sodium fluoride, and fluorosilicate, and particularly preferred salts include stannous bromide, chloride, sulfate, nitrate, and oxide. [0021]
In some cases, stable aqueous solutions are more readily prepared by adding water to the salt, rather than the reverse order of addition. For example, it was determined in the course of work in support of the invention that highly concentrated aqueous stannous chloride solutions, i.e. up to 90 weight percent SnCl[0022] ₂, can be conveniently prepared by adding water to stannous chloride in the desired weight ratio and stirring for a brief period of time. Dissolution was enhanced by using slighly acidified water.
The salt or aqueous solution is added to a distributive water system in an amount needed to produce a desired concentration of tin, as described above, in the water system. The concentration of Sn[0023] ⁺²in the water system may then be monitored, by techniques known in the art, and adjusted as necessary to maintain the desired concentration.
Aqueous stannous chloride solutions containing 50 weight percent SnCl[0024] ₂were prepared by adding water to the solid, in the manner described above. In the following experiments, samples of these solutions were added to samples of municipal drinking water effective to provide final concentrations of 0.15 to 1.0 ppm stannous chloride in the water, as shown.
To produce the data shown in Table 1, samples of the metals shown were immersed in samples of municipal drinking water, containing about 3 ppm of the conventional corrosion inhibitor sodium hexametaphosphate (HMP), from a system located in the upper midwestern region of the U.S. The test was carried out according to the procedure described in Materials and Methods, below. Corrosion rates, expressed in mils per year, were determined after 7 days at 120° F. in aerated water samples with and without 0.25 ppm added SnCl[0025] ₂. As shown in the Table, significant decreases in corrosion were observed in the SnCl₂-treated samples, especially with respect to carbon steel, copper and lead corrosion.

TABLE 1

No added SnCl₂ 0.25 ppm SnCl₂

Metal Rate, MPY Rate, MPY

Carbon Steel 40.2 2.1

Brass (CDA-443) 0.43 0.15

Copper 0.71 0.00

Lead 1.80 0.09
To obtain the data shown in Table 2, a specimen of each metal was suspended in a sample of municipal drinking water from Oklahoma (designated OKC) in a one-liter flask equipped with a condenser, gas delivery inlet, and thermometer. The contents of each flask were heated to 120° F. under a continuous air flow (1.5 cu ft/min) for seven days. Corrosion rates are again expressed as mils per year; nd=not determined. Various concentrations of SnCl[0026] ₂were used, as shown. As the data show, very low concentrations of SnCl₂were effective in reducing corrosion.

TABLE 2

Treated (SnCl₂) Rates, MPY

No added SnCl₂* 0.15 0.25 0.50 1.0

Metal Rate, MPY ppm ppm ppm ppm

Lead 1.2 nd 0.13 0.06 0.00

CDA-443 Brass 0.43 0.23 nd 0.02 nd

CDA-120 Copper 0.71 nd 0.00 nd nd
II. Corrosion Inhibition by Stannous Chloride in the Presence of Phosphate Additives [0027]
Currently, municipal water supplies frequently contain, as corrosion inhibiting additives, phosphates and/or zinc salts. For example, samples of OKC drinking water used in the experiments described herein contain, unless otherwise indicated, 3 ppm sodium hexametaphosphate. Therefore, experiments were carried out to examine the comparative and additive effects of aqueous stannous chloride and the phosphate additives already in use. [0028]
Table 3 shows corrosion rates in MPY for various metals in OKC water (aerated at 120° F., as described for Table 2) containing 3 ppm hexametaphosphate (as received) with and without other additives. The results show that increasing the amount of phosphate had variable results, depending on the metal tested; in some cases corrosion increased (e.g. for lead). Addition of zinc chloride gave moderate improvements, except in the case of lead. Addition of stannous chloride, however, reduced corrosion significantly, as is most apparent from a comparison of the 3[0029] ^rdand 5^thdata columns.

TABLE 3

Additive^a

3 ppm HMP

3 ppm HMP 3 ppm HMP 3 ppm OP 6 ppm HMP 6 ppm HMP

Metal (as received) 3 ppm OP 6 ppm HMP 0.5 ppm SnCl₂ 0.5 ppm SnCl₂ 0.1 ppm Zn⁺²

1018 41.3 25.7 29.5 18.6 11.4 24.3

Carbon

Steel

CDA-443 0.49 0.28 1.40 0.19 0.02 0.98

Brass

CDA-120 0.72 0.28 0.90 0.00 0.00 0.28

Copper

Lead 1.21 2.19 1.10 0.90 0.00 1.13
Table 4 gives further data for carbon steel corrosion (aerated at 120° F., as described above), showing combinations of SnCl[0030] ₂with varying amounts of phosphate. As shown in the Table, addition of SnCl₂reduced corrosion in all cases, although it appeared to be more effective at lower levels (3 ppm vs. 6 ppm) of phosphate.

TABLE 4

(Carbon Steel)

ppm HMP ppm SnCl₂ Corrosion, MPY

3 (as received) 0 41.3

3 0.25 6.8

3 0.50 7.6

6 (3 ppm added) 0 29.5

6 0.25 13.3

6 0.50 11.4

3 (as received, plus 0.25 11.1

3 ppm OP added)
To produce the data in Table 5, a sample of OKC water was obtained which had been filtered and disinfected but not treated with phosphate. Corrosion rates were determined for carbon steel in heated, aerated water as described above. [0031]

TABLE 5

(Carbon Steel)

ppm HMP ppm SnCl₂ Corrosion, MPY

0 0 49.3

3 0 21.1

3 0.25 13.3

0 0.25 2.1
III. Copper Corrosion Inhibition by SnCl[0032] ₂in the Presence of a Polymeric Dispersant or Metal Chelator
As noted above, the present anticorrosive stannous salt compositions may be used in combination with components which do not materially affect the metal corrosion inhibiting characteristic(s) of the composition. Such components would typically be substances added to a distributive water stream for purposes other than inhibition of corrosion. For example, dispersing or chelating agents, such as soluble anionic polymers (e.g. polyacrylates or acrylate copolymers), may be employed to reduce scale formation on solid surfaces. One such polymer, Acumer® 2100 (Rohm & Haas), an acrylate/sulfonate copolymer, was added to test systems such as described above. In these tests, the metal coupons were copper (CDA-110), and the water was municipal drinking water from LaSalle, Ill., which contained no phosphate additives. Test conditions were as described in Materials and Methods, below (120° F., aerated water, 7 days duration). [0033]
As shown below, the copolymer had no adverse properties on the corrosion inhibiting properties of SnCl[0034] ₂. Although larger concentrations of the copolymer alone appeared to increase corrosion, this effect was very effectively counteracted by the presence of SnCl₂.

Also shown in Table 6 is a combination of SnCl ₂with AMP (aminotris(methylenephosphonic acid); Mayoquest® 1320), which is useful in scale control by sequestering calcium and magnesium as well as ferrous ion. Again, the metal coupon showed very low corrosion in the presence of this additive and low concentrations of SnCl₂.

TABLE 6


(Copper)

		Corrosion
Additive	SnCl₂, ppm	Rate, MPY

Acumer ® 2100, 0.25 ppm	0	1.80
Acumer ® 2100, 0.25 ppm	0.25	0.0
Acumer ® 2100, 3 ppm	0	29.3
Acumer ® 2100, 3 ppm	0.50	0.0
AMP, 0.25 ppm	0	1.80
AMP, 0.25 ppm	0.25	0.08

IV. Lead Corrosion Inhibition at Varying pH [0036]

A series of tests was run to determine the effectiveness of conventional corrosion inhibitors and SnCl ₂on lead coupons at varying pH. Drinking water from Fall River, Mass., having no phosphate additives as received, was used for the tests, using the methods described above. pH was determined using EM Reagents ColorpHast® indicator strips.

TABLE 7


(Lead)

		Corrosion
pH	Treatment	Rate, MPY

5.3	None	0.64
5.3^(a)	3 ppm OP	3.43
5.3	3 ppm HMP	4.60
7.2	None	2.00
7.2	3 ppm OP	3.39
7.2	3 ppm HMP	2.10
7.2	0.25 ppm SnCl₂	0.03

As shown in Table 7, corrosion was greater in untreated water at higher pH, which may be partially due to the somewhat higher solubility of lead oxide under these conditions. Both sodium orthophosphate (OP) and sodium hexametaphosphate (HMP) increased the corrosion, particularly under acidic conditions, producing a reddish-yellow corrosion product (lead oxides) on the metal. However, corrosion was minimal in the sample containing 0.25 ppm SnCl[0038] ₂.
While the invention has been described with reference to specific methods and embodiments, it will be appreciated that various modifications may be made without departing from the invention. [0039]

MATERIALS & METHODS

A typical corrosion test was carried out in the following manner. The test sample of municipal drinking water was placed in a one liter resin kettle equipped to hold (1) a jacketed water cooled condenser, (2) a mounted air-injection gas tube, and (3) a holder from which the test specimen was suspended and totally immersed in the test water. The complete assembly was placed in a constant temperature oil bath. The test water was agitated by compressed air at a flow rate of 1.5 ft[0040] ³/min. The temperature was maintained at 120° F. for seven days.
Test coupons were generally 1″×2″×{fraction (1/16)}″ in size, with a ¼″ mounting hold centered ¼″ from one end. The test coupons were weighed before and after testing, and weight loss in milligrams was converted to a corrosion rate of milliinches per year (mpy). [0041]

Claims

It is claimed:

1. A method for inhibiting corrosion of corrodible metal in contact with water in a distributive water system, comprising

(a) adding to said water system, a composition consisting essentially of a stannous salt of a non-carbon acid, or an aqueous solution thereof,

and (b) maintaining in said water system a concentration of said stannous salt which corresponds to a concentration of tin between about 0.01 ppm and about 75 ppm.

2. The method of

claim 1

, wherein the stannous salt is selected from the group consisting of stannous bromide, chloride, sulfate, nitrate, oxide, pyrophosphate, perchlorate, tetrafluoroborate, monofluorophosphate, ammonium fluoride, sodium fluoride, and fluorosilicate.

3. The method of

claim 2

, wherein the stannous salt is selected from the group consisting of stannous bromide, chloride, sulfate, nitrate, and oxide.

4. The method of

claim 1

, wherein the concentration of stannous salt is maintained in the water system at a concentration which corresponds to a concentration of tin between about 0.05 ppm and about 25 ppm.

5. The method of

claim 1

, wherein in step (i) the stannous salt is added in the form of an aqueous solution.

6. The method of

claim 1

, wherein the corrodible metal is selected from the group consisting of a ferrous metal, a brass metal, a copper-containing metal, and a lead-containing metal.

7. The method of

claim 1

, wherein the distributive water system is a municipal drinking water system.

8. The method of

claim 1

, wherein the water system contains an alkali metal phosphate selected from a pyrophosphate, an orthophosphate, a hexametaphosphate, a hypophosphate, and a polyphosphate.

9. The method of

claim 8

, wherein the alkali metal phosphate is present in an amount effective to provide a concentration of about 0.01 ppm to about 5 ppm in the water system.

10. The method of

claim 1

, wherein the water system is treated to contain at least one component selected from a dispersing agent, a chelating agent, and a biocide.

11. A method for inhibiting corrosion of corrodible metal in contact with water in a distributive water system, comprising

(a) adding to said water system, a composition consisting essentially of (i) a stannous salt of a non-carbon acid, or an aqueous solution thereof, abd (ii) an alkali metal phosphate selected from a pyrophosphate, an orthophosphate, a hexametaphosphate, a hypophosphate, and a polyphosphate,

12. The method of

claim 11

, wherein the stannous salt is selected from the group consisting of tannous bromide, chloride, sulfate, nitrate, oxide, pyrophosphate, perchlorate, tetrafluoroborate, monofluorophosphate, ammonium fluoride, sodium fluoride, and fluorosilicate.

13. The method of

claim 12

14. The method of

claim 11

15. The method of

claim 1

16. The method of

claim 11

, wherein the alkali metal phosphate is added in an amount effective to provide a concentration of about 0.01 ppm to about 5 ppm in said water system.

17. The method of

claim 11

, wherein the alkali metal phosphate is sodium hexametaphosphate or sodium orthophosphate.

18. A metal corrosion inhibiting composition for use in a distributive water system, consisting essentially of (i) a stannous salt of a non-carbon acid or an aqueous solution thereof, and (ii) an alkali metal phosphate selected from a pyrophosphate, an orthophosphate, a hexametaphosphate, a hypophosphate, and a polyphosphate.

19. The composition of

claim 18

20. The composition of

claim 19

21. The composition of

claim 20

, wherein the stannous salt is stannous sulfate.

22. The composition of

claim 18

, wherein the stannous salt and the alkali metal phosphate are present in relative amounts effective to produce concentrations of about 0.01 to about 75 ppm tin and about 0.01 ppm to about 5 ppm alkali metal phosphate, respectively, in a distributive water system.

23. The composition of

claim 18

, further comprising at least one component selected from a dispersing agent, a chelating agent, and a biocide.

24. The composition of

claim 23

, wherein said component is an acrylate copolymer.