US3705786A - Corrosion inhibition with methylene bis-benzoic acid - Google Patents
Corrosion inhibition with methylene bis-benzoic acid Download PDFInfo
- Publication number
- US3705786A US3705786A US92174A US3705786DA US3705786A US 3705786 A US3705786 A US 3705786A US 92174 A US92174 A US 92174A US 3705786D A US3705786D A US 3705786DA US 3705786 A US3705786 A US 3705786A
- Authority
- US
- United States
- Prior art keywords
- benzoic acid
- methylene bis
- corrosion inhibition
- corrosion
- water
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 230000007797 corrosion Effects 0.000 title abstract description 19
- 238000005260 corrosion Methods 0.000 title abstract description 19
- 230000005764 inhibitory process Effects 0.000 title abstract description 5
- NKGDIYDBPVBXBW-UHFFFAOYSA-N 2-[(2-carboxyphenyl)methyl]benzoic acid Chemical compound OC(=O)C1=CC=CC=C1CC1=CC=CC=C1C(O)=O NKGDIYDBPVBXBW-UHFFFAOYSA-N 0.000 title description 3
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 abstract description 9
- -1 3,3''-METHYLENE Chemical class 0.000 abstract description 8
- 239000000463 material Substances 0.000 abstract description 8
- 239000005711 Benzoic acid Substances 0.000 abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 239000003112 inhibitor Substances 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- RBQRPOWGQURLEU-UHFFFAOYSA-N 3-[(3-carboxyphenyl)methyl]benzoic acid Chemical compound OC(=O)C1=CC=CC(CC=2C=C(C=CC=2)C(O)=O)=C1 RBQRPOWGQURLEU-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 5
- 229960004365 benzoic acid Drugs 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- WHRZCXAVMTUTDD-UHFFFAOYSA-N 1h-furo[2,3-d]pyrimidin-2-one Chemical compound N1C(=O)N=C2OC=CC2=C1 WHRZCXAVMTUTDD-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 235000006173 Larrea tridentata Nutrition 0.000 description 3
- 244000073231 Larrea tridentata Species 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229960002126 creosote Drugs 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000007769 metal material Substances 0.000 description 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000003134 recirculating effect Effects 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- FCSHMCFRCYZTRQ-UHFFFAOYSA-N N,N'-diphenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)NC1=CC=CC=C1 FCSHMCFRCYZTRQ-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- RTTYUVRWRMVNSA-UHFFFAOYSA-M [Cl-].C(CCCCCCCCCCC)[N+](C(C)C)(C)CC1=CC=CC=C1 Chemical compound [Cl-].C(CCCCCCCCCCC)[N+](C(C)C)(C)CC1=CC=CC=C1 RTTYUVRWRMVNSA-UHFFFAOYSA-M 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000010960 cold rolled steel Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013058 crude material Substances 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
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
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
- C23F11/12—Oxygen-containing compounds
- C23F11/124—Carboxylic acids
Definitions
- a number of materials are conventionally employed to inhibit corrosion particularly with respect to ferrous materials, e.g., steel.
- Such materials include inorganic compounds such as phosphates, chromates, nitrates, etc., organic compounds such as triethylamine, propylenediamine, picoline, tertiary butyl phenol, diphenylthiourea, lignin sulfonates, and surface active agents such as the anionic surfactants, e.g., alkyl aryl sulfonates, sodium N-methyl N-acyl taurates, etc., the anionic surfactants, e.g., fatty acid esters of higher polyglycols, ethylene oxide condensates, and the cationic surfactants, e.g., lauryl dimethylbenzyldimethyl ammonium chloride, etc.
- inhibitors are deficient in some respect, i.e., with regard to effectiveness, compatability with additives or other components of the system sustained effectiveness, and the like.
- a deficiency of particular importance is the effect on the ecology When such materials are discharged from the system in which they are functioning, particularly the accelerated growth of algae resulting from contact with phosphates.
- Chromates and phenols are also preferably avoided as corrosion inhibitors because of the undesirable effects on ecology.
- a corrosion inhibitor has now been found which is not susceptible to the deficiencies of the prior art.
- the indicated compound is employed in a recirculating water system, i.e., both heating and cooling systems.
- the above-indicated compound is preferably added to the system as an alkali metal or ammonium salt.
- 3,3'-methylene bis-benzoic acid is not detrimental to the ecology, i.e., will not deleteriously interfere with plant or animal life if discharged into streams.
- the present invention is directed to the employment of 3,3-methylene bis-benzoic acid in an aqueous environment as a corrosion inhibitor.
- the compound is preferably added to the system as an alkali metal or ammonium salt.
- the level of inhibitor employed is not critical; the particular level employed is determined at the option of the operator depending upon the degree of protection desired, the severity of the operating conditions, etc. A range of 60 to 150 ppm. in water, preferably ppm. is generally employed. It should be understood, that if desired, levels ,in excess of ppm. or less than 60 p.p.m. may be utilized in a given system.
- Example I The compound was prepared by the method of Schopff (Berichte 27, II, pp. 2321-2326, May-July 1894). Two hundred and fifty grams (2 moles) of benzoic acid were dissolved in 1500 grams concentrated sulfuric acid contained in a 2 liter flask. The flask was set in an ice-bath and the temperature (which rose due to heat of solution) was allowed to drop to 20 C.; 110 ml. of 37% formaldehyde solution (1.2 moles HCHO) were introduced slowly with stirring and swirling. After the heat and fumes had dissipated, the flask was stoppered and allowed to stand for 5 days; at the end of this time, the liquid was brown and had no odor of formaldehyde.
- Schopff Berichte 27, II, pp. 2321-2326, May-July 1894.
- the flask contents were poured into a mixture of 1500 ml. water and 1500 grams of ice and the crude yellow product which precipitated was filtered off on a Buchner funnel. This crude material was washed several times with cold water, then 250 ml. ammonia and 1500 ml. of water were added to dissolve it. The resulting green solution was treated with 3 grams of activated carbon and filtered, then the acid reprecipitated with 50% sulfuric acid, and cooled. The precipitate was filtered on a Buchner funnel, washed with cold water, and then the mass was broken up in a large beaker and stirred thoroughly with hot (70 C.) water.
- the material was filtered again and further washed on the funnel with hot water (a total of 5 liters of hot water was used).
- the product was dried in a vacuum oven at 50 C. overnight. No sharp melting point was found; sintering occurred between and 200 C., melting from 220-230 C.
- Sheets of mild cold rolled steel 0.036 inch thick were cut into strips /2 inch wide and 2 inches long, and were wire-brushed, degreased, cleaned in 10% hydrochloric acid, rinsed with distilled water and then with acetone, dried, and stored in a dessicator until ready for use.
- test tubes 38 mm. in diameter and 200 mm. long which were held in a water bath maintained at 50 C.-* -l C.
- Each test tube contained a twoholed rubber stopper, one hole of which contained a glass tube 3 mm. in inside diameter, which reached to the bottom of the test tube.
- the narrow glass tubing was used to aerate the water; laboratory compressed air was passed through a flask containing water, for humidification, and thence through the test solutions. Test usually lasted 5 days, during which time the air passed through the test tubes for 16 hours of each 24; for the remaining 8 hours, no air was admitted.
- the novel inhibitor of the present invention may be employed in any aqueous environment where corrosion of ferrous metal in the system is a problem.
- Such systems include, but are not limited to, recirculating water systems, tanks, pipelines, radiators, and other aqueous based can be seen that virtually ferrous metal contacting systems.
- superior corrosion inhibitor characteristics can be achieved by adding to creosote compositions 3,3-methylene bis-benzoicacid at a level ranging from 0.05 to 1%, preferably 0.1% by weight, based on the weight of the creosote composition.
- the employment of such creosote compounds in the conventional manner results in minimization or elimination of corrosion generally encountered in such situations, when the creosote also contains pentachlorophenol as an adjuvant to its protective action.
- the method of inhibiting corrosion of ferrous metal materials which comprises contacting said metal in an aqueous environment with an effective amount of 3,3- methylene bis-benzoic acid.
- the method of inhibiting corrosion of ferrous metal materials which comprises contacting said metal with methylene bis-benzoic acid in an aqueous solution at a level ranging from to 150 ppm.
Landscapes
- 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)
Abstract
THIS APPLICATION IS DIRECTED TO CORROSION INHIBITION OF FERROUS MATERIALS IN AN AQUEOUS ENVIRONMENT BY EMPLOYING 3,3''-METHYLENE BIS-BENZOIC ACID.
Description
United States Patent O) CORROSION INHIBITION WITH METHYLENE BIS-BENZOIC ACID Saul Kaye, Evanston, Ill., assignor to Ventron Corporation, Beverly, Mass. No Drawing. Filed Nov. 23, 1970, Ser. No. 92,174 Int. Cl. C23f 11/12 U.S. Cl. 212.7 4 Claims ABSTRACT OF THE DISCLOSURE This application is directed to corrosion inhibition of ferrous materials in an aqueous environment by employing 3,3'-methylene bis-benzoic acid.
BACKGROUND OF THE INVENTION A number of materials are conventionally employed to inhibit corrosion particularly with respect to ferrous materials, e.g., steel. Such materials include inorganic compounds such as phosphates, chromates, nitrates, etc., organic compounds such as triethylamine, propylenediamine, picoline, tertiary butyl phenol, diphenylthiourea, lignin sulfonates, and surface active agents such as the anionic surfactants, e.g., alkyl aryl sulfonates, sodium N-methyl N-acyl taurates, etc., the anionic surfactants, e.g., fatty acid esters of higher polyglycols, ethylene oxide condensates, and the cationic surfactants, e.g., lauryl dimethylbenzyldimethyl ammonium chloride, etc.
However, such inhibitors are deficient in some respect, i.e., with regard to effectiveness, compatability with additives or other components of the system sustained effectiveness, and the like. A deficiency of particular importance is the effect on the ecology When such materials are discharged from the system in which they are functioning, particularly the accelerated growth of algae resulting from contact with phosphates. Chromates and phenols are also preferably avoided as corrosion inhibitors because of the undesirable effects on ecology.
A corrosion inhibitor has now been found which is not susceptible to the deficiencies of the prior art.
SUMMARY OF THE INVENTION The present invention is directed to the employment of the compound:
COOH COOH 3,3'-methylene bis-benzoic acid in an aqueous environment in contact with ferrous materials. In a particularly preferred embodiment, the indicated compound is employed in a recirculating water system, i.e., both heating and cooling systems. The above-indicated compound is preferably added to the system as an alkali metal or ammonium salt.
In addition to being a highly efficient corrosion inhibitor, thus significantly lengthening the life of the equipment, 3,3'-methylene bis-benzoic acid is not detrimental to the ecology, i.e., will not deleteriously interfere with plant or animal life if discharged into streams.
DETAILED DESCRIPTION OF THE INVENTION The present invention is directed to the employment of 3,3-methylene bis-benzoic acid in an aqueous environment as a corrosion inhibitor. As stated above, the compound is preferably added to the system as an alkali metal or ammonium salt.
The level of inhibitor employed is not critical; the particular level employed is determined at the option of the operator depending upon the degree of protection desired, the severity of the operating conditions, etc. A range of 60 to 150 ppm. in water, preferably ppm. is generally employed. It should be understood, that if desired, levels ,in excess of ppm. or less than 60 p.p.m. may be utilized in a given system.
The preparation of 3,3'-methylene bis-benzoic acid is known to the art. For example, the method set forth in U.S. Pat. No. 3,113,148 or Berichte 27, II, pp. 2321-2326, may be employed.
The following nonlimiting example illustrates the prep aration of 3,3'-methylene bis-benzoic acid.
Example I The compound was prepared by the method of Schopff (Berichte 27, II, pp. 2321-2326, May-July 1894). Two hundred and fifty grams (2 moles) of benzoic acid were dissolved in 1500 grams concentrated sulfuric acid contained in a 2 liter flask. The flask was set in an ice-bath and the temperature (which rose due to heat of solution) was allowed to drop to 20 C.; 110 ml. of 37% formaldehyde solution (1.2 moles HCHO) were introduced slowly with stirring and swirling. After the heat and fumes had dissipated, the flask was stoppered and allowed to stand for 5 days; at the end of this time, the liquid was brown and had no odor of formaldehyde. The flask contents were poured into a mixture of 1500 ml. water and 1500 grams of ice and the crude yellow product which precipitated was filtered off on a Buchner funnel. This crude material was washed several times with cold water, then 250 ml. ammonia and 1500 ml. of water were added to dissolve it. The resulting green solution was treated with 3 grams of activated carbon and filtered, then the acid reprecipitated with 50% sulfuric acid, and cooled. The precipitate was filtered on a Buchner funnel, washed with cold water, and then the mass was broken up in a large beaker and stirred thoroughly with hot (70 C.) water. The material was filtered again and further washed on the funnel with hot water (a total of 5 liters of hot water was used). The product was dried in a vacuum oven at 50 C. overnight. No sharp melting point was found; sintering occurred between and 200 C., melting from 220-230 C.
The effectiveness of 3,3'-methylene bis-benzoic acid as a corrosion inhibitor was determined by the following procedure.
Sheets of mild cold rolled steel 0.036 inch thick were cut into strips /2 inch wide and 2 inches long, and were wire-brushed, degreased, cleaned in 10% hydrochloric acid, rinsed with distilled water and then with acetone, dried, and stored in a dessicator until ready for use.
Two such coupons were immersed in 100 ml. of tap water containing the corrosion inhibitor in dissolved form, Whose pH had been adjusted to 6-8. The test solutions were contained in test tubes 38 mm. in diameter and 200 mm. long which were held in a water bath maintained at 50 C.-* -l C. Each test tube contained a twoholed rubber stopper, one hole of which contained a glass tube 3 mm. in inside diameter, which reached to the bottom of the test tube. The narrow glass tubing was used to aerate the water; laboratory compressed air was passed through a flask containing water, for humidification, and thence through the test solutions. Test usually lasted 5 days, during which time the air passed through the test tubes for 16 hours of each 24; for the remaining 8 hours, no air was admitted.
At the end of the exposure period, coupons were removed, rubbed free of deposit, cleaned by exposure to 10% HCl for 30 seconds, rinsed, scrubbed with a nylon brush, wiped dry, wiped with acetone, dried, and weighed. In every test all coupons were the same size, and control. solutions containing only tap water were used as un- 75 TABLE Corrosion, as percent of unprotected coupon 3,3-methyl- P.p.m. of compound Benzoic ene bis-benin solution 1 acid zolc acid From the above table, it complete corrosion inhibition is achieved at a relatively low level with the corrosion inhibitor of the present invention. That relatively large quantities of a related compound are required to even approach the effectiveness achieved by the compound of the present invention at a low level, indicates the unobviousness of the present invention.
The novel inhibitor of the present invention may be employed in any aqueous environment where corrosion of ferrous metal in the system is a problem. Such systems include, but are not limited to, recirculating water systems, tanks, pipelines, radiators, and other aqueous based can be seen that virtually ferrous metal contacting systems. It has also been found unexpectedly that superior corrosion inhibitor characteristics can be achieved by adding to creosote compositions 3,3-methylene bis-benzoicacid at a level ranging from 0.05 to 1%, preferably 0.1% by weight, based on the weight of the creosote composition. The employment of such creosote compounds in the conventional manner results in minimization or elimination of corrosion generally encountered in such situations, when the creosote also contains pentachlorophenol as an adjuvant to its protective action.
I claim:
1. The method of inhibiting corrosion of ferrous metal materials which comprises contacting said metal in an aqueous environment with an effective amount of 3,3- methylene bis-benzoic acid.
2. The method as defined in claim 1 wherein said ferrous metal is steel.
3. The method of inhibiting corrosion of ferrous metal materials which comprises contacting said metal with methylene bis-benzoic acid in an aqueous solution at a level ranging from to 150 ppm.
4. The method as defined in claim 3 wherein said 3,3- methylene bis-benzoic acid is employed at a level of ppm.
References Cited UNITED STATES PATENTS 3,113,14'8 12/1963 Le Blane et a1. 260-515 P LEON D. ROSDOL, Primary Examiner I. GLUCK, Assistant Examiner US. Cl. X.R.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9217470A | 1970-11-23 | 1970-11-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3705786A true US3705786A (en) | 1972-12-12 |
Family
ID=22232001
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US92174A Expired - Lifetime US3705786A (en) | 1970-11-23 | 1970-11-23 | Corrosion inhibition with methylene bis-benzoic acid |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3705786A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3928430A (en) * | 1974-07-19 | 1975-12-23 | Koppers Co Inc | Method for the preparation of 3,3-methylenebis (benzoic acid) |
| US4093557A (en) * | 1976-09-16 | 1978-06-06 | Hercules Incorporated | Process for inhibiting corrosion of metals in aqueous systems |
| US4263167A (en) * | 1979-06-29 | 1981-04-21 | Union Carbide Corporation | Poly(alkylene oxide) compositions |
-
1970
- 1970-11-23 US US92174A patent/US3705786A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3928430A (en) * | 1974-07-19 | 1975-12-23 | Koppers Co Inc | Method for the preparation of 3,3-methylenebis (benzoic acid) |
| US4093557A (en) * | 1976-09-16 | 1978-06-06 | Hercules Incorporated | Process for inhibiting corrosion of metals in aqueous systems |
| US4263167A (en) * | 1979-06-29 | 1981-04-21 | Union Carbide Corporation | Poly(alkylene oxide) compositions |
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