US2413495A - Phosphoric acid detergent - Google Patents
Phosphoric acid detergent Download PDFInfo
- Publication number
- US2413495A US2413495A US2413495DA US2413495A US 2413495 A US2413495 A US 2413495A US 2413495D A US2413495D A US 2413495DA US 2413495 A US2413495 A US 2413495A
- Authority
- US
- United States
- Prior art keywords
- phosphoric acid
- acid
- composition
- cleansers
- ether sulfonate
- 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
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 title description 86
- 229910000147 aluminium phosphate Inorganic materials 0.000 title description 36
- 239000003599 detergent Substances 0.000 title description 16
- 239000000203 mixture Substances 0.000 description 68
- 235000011007 phosphoric acid Nutrition 0.000 description 44
- RZXLPPRPEOUENN-UHFFFAOYSA-N Chlorfenson Chemical compound C1=CC(Cl)=CC=C1OS(=O)(=O)C1=CC=C(Cl)C=C1 RZXLPPRPEOUENN-UHFFFAOYSA-N 0.000 description 40
- 239000002253 acid Substances 0.000 description 24
- 238000005260 corrosion Methods 0.000 description 24
- 239000000839 emulsion Substances 0.000 description 24
- OOHAUGDGCWURIT-UHFFFAOYSA-N N,N-dipentylpentan-1-amine Chemical compound CCCCCN(CCCCC)CCCCC OOHAUGDGCWURIT-UHFFFAOYSA-N 0.000 description 22
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 18
- MUBZPKHOEPUJKR-UHFFFAOYSA-N oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 18
- 238000004140 cleaning Methods 0.000 description 16
- 239000002184 metal Substances 0.000 description 14
- 229910052751 metal Inorganic materials 0.000 description 14
- 239000000080 wetting agent Substances 0.000 description 14
- 239000003795 chemical substances by application Substances 0.000 description 12
- 230000002378 acidificating Effects 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 210000004080 Milk Anatomy 0.000 description 6
- 229910000831 Steel Inorganic materials 0.000 description 6
- LSNNMFCWUKXFEE-UHFFFAOYSA-L Sulphite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 6
- 125000005037 alkyl phenyl group Chemical group 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- 231100000078 corrosive Toxicity 0.000 description 6
- 231100001010 corrosive Toxicity 0.000 description 6
- -1 ether halide Chemical class 0.000 description 6
- 150000002739 metals Chemical class 0.000 description 6
- 239000008267 milk Substances 0.000 description 6
- 235000013336 milk Nutrition 0.000 description 6
- 235000006408 oxalic acid Nutrition 0.000 description 6
- 239000002689 soil Substances 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- WQZGKKKJIJFFOK-GASJEMHNSA-N D-Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 4
- 206010022114 Injury Diseases 0.000 description 4
- 125000004104 aryloxy group Chemical group 0.000 description 4
- 238000010790 dilution Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 230000001804 emulsifying Effects 0.000 description 4
- 150000002170 ethers Chemical class 0.000 description 4
- 239000008103 glucose Substances 0.000 description 4
- 239000003292 glue Substances 0.000 description 4
- 230000002401 inhibitory effect Effects 0.000 description 4
- 235000013379 molasses Nutrition 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 229920001281 polyalkylene Polymers 0.000 description 4
- 239000004575 stone Substances 0.000 description 4
- 230000002195 synergetic Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 238000009736 wetting Methods 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate dianion Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K [O-]P([O-])([O-])=O Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 230000002152 alkylating Effects 0.000 description 2
- 230000004075 alteration Effects 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000004432 carbon atoms Chemical group C* 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 2
- 238000005345 coagulation Methods 0.000 description 2
- 235000013365 dairy product Nutrition 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 239000008233 hard water Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 230000001737 promoting Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000007790 solid phase Substances 0.000 description 2
- 238000004642 transportation engineering Methods 0.000 description 2
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
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G1/00—Cleaning or pickling metallic material with solutions or molten salts
- C23G1/02—Cleaning or pickling metallic material with solutions or molten salts with acid solutions
- C23G1/04—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors
- C23G1/06—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors organic inhibitors
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/06—Phosphates, including polyphosphates
Definitions
- This invention pertains to compositions comprising phosphoric acid combined with agents to form improved acidic cleansers, and generally to improve uses of phosphoric acid for various cleansing purposes, particularly when metallic surfaces are involved, this application being a continuation-in-'part of my application Serial Number 343,494, led July 1, 1940.
- Cleansing agents' generally are alkaline or basic in character. Such are ordinary soap, or various salts such as phosphate or carbonate cleansers. Many of these agents have good emulsifying effect and oftentimes are capable of cutting grease, but such alkaline reagents may be harmful to the materials being cleaned, and for certain types of cleaning and descaling operations are unsatisfactory or are less efcient than acidic cleansers.
- Acid cleansers have been the subject of numerous suggestions for improvement. Many materials used as acidic cleansers involve risk of corroding metals, and lack desirable properties such as wetting-out ability 'and emulsifying power. However, because of their ability to function in the removal of certain types of soil and scales better than alkaline cleansers, they are utilized in spite of these disadvantages. For example, oxalic acid has been used rto clean railway or street cars where traffic film or smoky grime are to be removed. But to giveadequate body to oxalic acid cleansers, it is extensive practice to add substances such as molasses or glue or glucose. Such solutions do not readily penetrate a grimy film such as on railway coaches, but require considerable rubbing; nor do they readily ow nor rinse quickly from surfaces being cleaned.
- An Object of this invention is to provide acid cleansers that are effective to remove various sorts of soil or scale with minimum of injury to exposed or underlying metal.
- a further object is to provide acid cleansers to remove oil, dirt and smoke from painted or lacquered surfaces such as railway coaches or automobiles, but without injury to the finish coat.
- Another object is to provide acid cleansers that rinse freely from the surface after cleansing.
- an object is to provide acid cleansers that do not require addition of such substances as glue, molasses or glucose.
- a specific Object is to increase the effectiveness and safety of phosphoric acid as a cleanser for various surfaces.
- a purpose of this invention is to improve the practicability of phosphoric acid forvarious cleansing uses where contact of the cleansers with metallic surfaces is involved, and more particularly to minimize corrosion of metals that may contact the acid.
- This invention provides unusually effective acid compositions comprising phosphoric acid in which is contained an aryloxy polyalkylene ether' sulfonate.
- This is an agent for lowering interfacial tension, promoting the wetting of the soil or scale by the acid solution, and contributing other desirable properties.
- wetting agents are known, many are not at all suitable for the purposes of this invention, lacking suitable stability in acid, or otherwise failing to provide the desirable properties of my invention.
- a sulfonated ether made, for example, by alkylating phenol with di-isobutylene; condensing the product with a dichloropolyalkvlene ether such as B-Bdichloroethyl ether to substitute only one of the halogen atoms by the alkylated phenol.
- This aryloxy polyalkylene ether halide is then sulfonated by reaction with suliite.
- Such a product is di-isobutyl phenyl diglycol ether sulfonate.
- this preferred cleanser is mentioned an aqueous composition containing about 2.5% orthophosphoric acid, 0.17% di-isobutyl, phenyl diglycol ether sulfonate. and 0.006%
- a suitable range of composition of this cleanser may be approximately 1% to 5% orthophosphoric acid, 0.03% to 1% alkyl phenyl glycol ether sulfonate emulsion, and 0.002% to 0.02% triamylamine.
- compositions of the preferred ether sulfonate wetting agent i. e. Triton-'120
- phosphoric acid i. e. Triton-'120
- Triton-720 is commonly available as a heavy aqueous emulsion having a density of about 1.06 relative to water, and containing about 30% sulfonate in about '70% water. Although it is characterized by unusually .good properties in acidic media, it will not form homogeneous compositions with phosphoric acid over all ranges of concentration. At certain concentrations the product separates into mutually insoluble liquid layers.
- composition containing '7.5% of the heavy, commercially obtainable, ether sulfonate emulsion should contain not more than 50% H3PO4 nor less than 25% HaP04.
- compositions within the scope of my invention there should be a sufficient amount of the ether sulfonate wetting agent to be effective under the conditions of use in adequately lowering the surface tension and wetting out time, and in promating the detergent action of the composition- 4 4 and its free rinsing qualities. It is undesirable to have more than this amount of ether sulfonate wetting agent relative to phosphoric acid, because such additional amounts do not further increase the desirable properties of the composition, but may add undesirably to the expense.
- compositions lying toward the apex of the area of stable compositions, as shown in the figure, provide adequate concentrations of ether sulfonate under many conditions of use.
- compositions which are homogeneous and stable, containing from about 20% to 53% of HaPO4 and from about 4% to 15% of ether sulfonate in the form of its heavy,
- the triamylamine in this composition is commercial. normal triamylamine, which contains some isomeric isotriamylamine. 'Ihe composition Concentration Reduction of Triton-7m in rate of in composition corrosion Per cent Per cent Similarly, the reduction in rate of corrosion of steel specimens during a 24- hour test, by the presence of triamylamine alone in phosphoric acid solutions containing 50.6% of HJPO; was as follows:
- This application is directed broadly to phosphoric acid combinations with alkylaryloxyalkylol and more particularly with alkyl phenyl glycol ether sulfonate.
- a detergent composition comprising an aqueous solution of phosphoric acid containing an aqueous emulsion of di-isobutyl phenyl diglycol ether sulfonate, and triamylamine, characterized by high non-corrosive property towards metals due to the synergistic corrosion inhibiting property of the ether sulfonate and triamylamine, one hundred percent by weight of the composition comprising from 4% to 15% of the ether sulfonate emulsion, from 20% to 53% of H3PO4, and from about 0.1% to 0.3% of triamylamine, the ether suifonate emulsion containing of the ether sulfonate.
Description
Dec. 31, 1946.
c. P. GIVEN 2,413,495
PHOSPHORIC ACID DETERGENT COMPOSITION Filed March 30, 1943 IOOX Uns a bZe 60% l SabZe 40% Q Composz'l'z'ons 20% Uns'a b2 e Commercial Ezer Sulfonae Emulsion (Conainer 50% aci'z've z'nyredz'em) Patented Dec. 31, 1946 PHOSPHORIC Acm mi''rxfzncflcrz'rv COMPOSITION Charles P. Given, Washington, D. C., assigner to Virginia-Carolina Chemical Corporation, Richmond, Va., a corporation of Virginia Application March 30, 1943, Serial No. 481,123
1 Claim. 1
This invention pertains to compositions comprising phosphoric acid combined with agents to form improved acidic cleansers, and generally to improve uses of phosphoric acid for various cleansing purposes, particularly when metallic surfaces are involved, this application being a continuation-in-'part of my application Serial Number 343,494, led July 1, 1940.
Cleansing agents', for illustration, generally are alkaline or basic in character. Such are ordinary soap, or various salts such as phosphate or carbonate cleansers. Many of these agents have good emulsifying effect and oftentimes are capable of cutting grease, but such alkaline reagents may be harmful to the materials being cleaned, and for certain types of cleaning and descaling operations are unsatisfactory or are less efcient than acidic cleansers.
Acid cleansers have been the subject of numerous suggestions for improvement. Many materials used as acidic cleansers involve risk of corroding metals, and lack desirable properties such as wetting-out ability 'and emulsifying power. However, because of their ability to function in the removal of certain types of soil and scales better than alkaline cleansers, they are utilized in spite of these disadvantages. For example, oxalic acid has been used rto clean railway or street cars where traffic film or smoky grime are to be removed. But to giveadequate body to oxalic acid cleansers, it is extensive practice to add substances such as molasses or glue or glucose. Such solutions do not readily penetrate a grimy film such as on railway coaches, but require considerable rubbing; nor do they readily ow nor rinse quickly from surfaces being cleaned.
.Moreover, their tendency to be sluggish in action and to be sluggish in removal, augments a fault of acids to corrode metal parts of surfaces being cleaned. This tendency to corrode metal parts is a serious problem in cleaning utensils used in the dairy industry. Such utensils become incrusted by deposits from milk, known as milk stone. Milk stone must be removed without impairment of the metal surface. After cleaning, the surfaces should be capable of being quickly rinsed, or at least be rapidly self-draining. The removal of certain types of hard-water scales from the surfaces of heat exchange equipment is another example where avoidance or reduction of corrosion is a factor of major im portance in practical use of acidic cleansers.
An Object of this invention is to provide acid cleansers that are effective to remove various sorts of soil or scale with minimum of injury to exposed or underlying metal. A further object is to provide acid cleansers to remove oil, dirt and smoke from painted or lacquered surfaces such as railway coaches or automobiles, but without injury to the finish coat. Another object is to provide acid cleansers that rinse freely from the surface after cleansing. Also, an object is to provide acid cleansers that do not require addition of such substances as glue, molasses or glucose. A specific Object is to increase the effectiveness and safety of phosphoric acid as a cleanser for various surfaces.
More broadly with respect to phosphoric acid, a purpose of this invention is to improve the practicability of phosphoric acid forvarious cleansing uses where contact of the cleansers with metallic surfaces is involved, and more particularly to minimize corrosion of metals that may contact the acid.
This invention provides unusually effective acid compositions comprising phosphoric acid in which is contained an aryloxy polyalkylene ether' sulfonate. This is an agent for lowering interfacial tension, promoting the wetting of the soil or scale by the acid solution, and contributing other desirable properties. Although numerous such agents, often termed wetting agents," are known, many are not at all suitable for the purposes of this invention, lacking suitable stability in acid, or otherwise failing to provide the desirable properties of my invention.
I prefer to utilize a sulfonated ether made, for example, by alkylating phenol with di-isobutylene; condensing the product with a dichloropolyalkvlene ether such as B-Bdichloroethyl ether to substitute only one of the halogen atoms by the alkylated phenol. This aryloxy polyalkylene ether halide is then sulfonated by reaction with suliite. Such a product is di-isobutyl phenyl diglycol ether sulfonate.
Specifically, I have used a material of this type, believed to be di-sobutyl phenyl diglycol ether sulfonate made in accordance with U. S. Patent No. 2,115,192, Bruson; and available under the trade name of Triton-720.
While addition of this material to phosphoric acid in accordance with my invention, as set forth below, has desirable effects not only from the point of view of detergent action, but also with respect to reducing the corrosive tendency the aliphatic groups contain fromV four to six carbon atoms. There is a synergistic action of this combination of agents with phosphoric acid according to my invention which was not known and which is an important part of my invention.
As an example of this preferred cleanser is mentioned an aqueous composition containing about 2.5% orthophosphoric acid, 0.17% di-isobutyl, phenyl diglycol ether sulfonate. and 0.006%
ltriamylamine. This composition has been found superior both to alkaline cleansers and to oxalic acid cleansers when used for the cleansing of street cars; its action being without the harmful effects of the former on enameled and vamished surfaces and metallic surfaces, and superior in its detergent and free rinsing qualities to the latter. Furthermore, operators prefer this compo sition as being easier to handle and less irritating to the hands.
A suitable range of composition of this cleanser may be approximately 1% to 5% orthophosphoric acid, 0.03% to 1% alkyl phenyl glycol ether sulfonate emulsion, and 0.002% to 0.02% triamylamine.
While such compositions are satisfactory for use in actual detergent or cleaning operations, it is desirable for economic reasons, including transportation, to market a product of much higher concentration which can be diluted as desired at the point of use. In this resides an additional element of my invention. While the marketing of concentrated products for dilution at point of use has long been known and practiced with respect to many products, mixtures of wetting agents in strong concentrations of acid are not generally adapted to such practice because o f the instability of organic wetting agents in strong acid solutions.
I have found that compositions of the preferred ether sulfonate wetting agent (i. e. Triton-'120), and phosphoric acid, are not stable in all proportions. The preferred ether sulfonate wetting agent (Triton-720) is commonly available as a heavy aqueous emulsion having a density of about 1.06 relative to water, and containing about 30% sulfonate in about '70% water. Although it is characterized by unusually .good properties in acidic media, it will not form homogeneous compositions with phosphoric acid over all ranges of concentration. At certain concentrations the product separates into mutually insoluble liquid layers. At others, there appears to be a coagulation of the dispersed solid phase which tends to collect at the surface of a liquid phase. Such instability is not desirable in a commercial product. I have found, however, that in certain concentrations a stable homogeneous emulsion may be formed, which is far superior, and is a preferred composition. Generally in the concentrated form preferred in my invention, the concentrations of phosphoric acid and ether sulfonate should be related as shown in the drawing, the sole figure of which is a graph defining limits within which desirably homogeneous compositions are obtained and outside of which there is a tendency for the composition to break down as described above.
For example, a composition containing '7.5% of the heavy, commercially obtainable, ether sulfonate emulsion, should contain not more than 50% H3PO4 nor less than 25% HaP04.
In compositions within the scope of my invention there should be a sufficient amount of the ether sulfonate wetting agent to be effective under the conditions of use in adequately lowering the surface tension and wetting out time, and in promating the detergent action of the composition- 4 4 and its free rinsing qualities. It is undesirable to have more than this amount of ether sulfonate wetting agent relative to phosphoric acid, because such additional amounts do not further increase the desirable properties of the composition, but may add undesirably to the expense.
Compositions lying toward the apex of the area of stable compositions, as shown in the figure, provide adequate concentrations of ether sulfonate under many conditions of use.
For example, I have used compositions which are homogeneous and stable, containing from about 20% to 53% of HaPO4 and from about 4% to 15% of ether sulfonate in the form of its heavy,
commercially available emulsion, or approximately 1.3% to 5% of the sulfonate itself/ More specifically, I find that homogeneous compositions within the range of 22% to 45% HaPOa and containing 4% to '1.5% of ether sulfonate emulsion have excellent properties and are preferred for many uses.
The triamylamine in this composition is commercial. normal triamylamine, which contains some isomeric isotriamylamine. 'Ihe composition Concentration Reduction of Triton-7m in rate of in composition corrosion Per cent Per cent Similarly, the reduction in rate of corrosion of steel specimens during a 24- hour test, by the presence of triamylamine alone in phosphoric acid solutions containing 50.6% of HJPO; was as follows:
Concentration of mamyb Reduction amine in 1n fate of composition wrrosion P" um Per cent 97.9 14 97' 4 The reduction in rate of corrosion of steel specimens during a 24-hour test, by compositions containing both the sulfonated ether emulsion and the triamylamine was determined to be as follows:
Concentrations in compositions of- Reduction in rate oi HgPO Triton-720 Triamylamine corrosion Per cent Per cent Per ccnl Per cen! 5i). li 7. 0. 20 99. 6 50. (l 7. 5 0. i4 99. fi 42. 2 25 0. ll 99. 5
These iigures show the unusual and beneiicial result obtained by the presence of both the triamylamine and the alkyl phenyl polyglycol ether sulfonate in reducing the corrosive properties of the composition. The rate of corrosion, reduced to slightly over 2% by the presence of the amine, is further cut to a fraction of one percent in the presence of both substances.
It should be pointed out at this point that as the emciency of the process approaches 100%, further increases in eiliciency are attained only with increasing diiliculty. Thus the importance of the result obtained by the combined presence oi' both agents with the phosphoric acid must be recognized.
Reducing the rate of corrosion from about 2.5% as obtained with the addition of amine alone, to about 0.5% in the presence of the combination constitutes a iive fold gain in the eirectiveness of the corrosion reduction. Moreover, upon dilution such Vcompositions maintain their high inhibition of corrosion. Thus in a dilute solution containing 5% H3PO4, with only 0.74% ether sulfonate emulsion and 0.012% triamylamine, reduction of the rate of corrosion of steel was still 95%.
This application is directed broadly to phosphoric acid combinations with alkylaryloxyalkylol and more particularly with alkyl phenyl glycol ether sulfonate.
While in accordance with the patent statutes I have described a preferred embodiment of this invention, it will now be apparent to those skilled in the art that modieations and alterations may be made within the scope of the appended claim.
What I claim as my invention is:
A detergent composition comprising an aqueous solution of phosphoric acid containing an aqueous emulsion of di-isobutyl phenyl diglycol ether sulfonate, and triamylamine, characterized by high non-corrosive property towards metals due to the synergistic corrosion inhibiting property of the ether sulfonate and triamylamine, one hundred percent by weight of the composition comprising from 4% to 15% of the ether sulfonate emulsion, from 20% to 53% of H3PO4, and from about 0.1% to 0.3% of triamylamine, the ether suifonate emulsion containing of the ether sulfonate.
CHARLES P. GIVEN.
Publications (1)
Publication Number | Publication Date |
---|---|
US2413495A true US2413495A (en) | 1946-12-31 |
Family
ID=3435337
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US2413495D Expired - Lifetime US2413495A (en) | Phosphoric acid detergent |
Country Status (1)
Country | Link |
---|---|
US (1) | US2413495A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2505785A (en) * | 1945-09-17 | 1950-05-02 | Howard R Moore | Method of producing a corrosion inhibitive coating on ferrous metals |
US2525178A (en) * | 1947-01-18 | 1950-10-10 | Turco Products Inc | Removing silver films from mirrors with phosphoric acid |
DE1074357B (en) * | 1960-01-28 | Mctallgesellschaft Aktiengesellschaft, Frankfurt/M | Alkaline, degreasing cleaner for metals | |
US2977315A (en) * | 1956-09-12 | 1961-03-28 | Lazarus Lab Inc | Water soluble iodine-phosphoric-acidsynthetic detergent composition |
-
0
- US US2413495D patent/US2413495A/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1074357B (en) * | 1960-01-28 | Mctallgesellschaft Aktiengesellschaft, Frankfurt/M | Alkaline, degreasing cleaner for metals | |
US2505785A (en) * | 1945-09-17 | 1950-05-02 | Howard R Moore | Method of producing a corrosion inhibitive coating on ferrous metals |
US2525178A (en) * | 1947-01-18 | 1950-10-10 | Turco Products Inc | Removing silver films from mirrors with phosphoric acid |
US2977315A (en) * | 1956-09-12 | 1961-03-28 | Lazarus Lab Inc | Water soluble iodine-phosphoric-acidsynthetic detergent composition |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0643127B1 (en) | Processes and compositions for improving the mobility of aluminium cans when conveyed by automatic conveying equipment | |
US2814593A (en) | Corrosion inhibition | |
US5705472A (en) | Neutral aqueous cleaning composition | |
US3960742A (en) | Water-dispersable solvent emulsion type cleaner concentrate | |
JPH0418000B2 (en) | ||
JPS6017829B2 (en) | Corrosion inhibitor for metal surfaces | |
US2802788A (en) | Cleaning composition for automotive | |
CA2177278A1 (en) | Wheel cleaning composition containing acid fluoride salts | |
US2741599A (en) | Composition for cleaning and stripping paint from aluminum | |
JPS63165496A (en) | Short chain alkanesulfonic acid-containing detergent and disinfectant | |
JPH10511123A (en) | Aqueous cleaning compositions based on maleic acid and uses thereof | |
US5196146A (en) | Aqueous cleaning formulation containing a 2-piperazinone, method of using the same and concentrate for preparing the same | |
US4772415A (en) | Heavy duty degreaser composition and method of use | |
US4174289A (en) | Liquid detergent-bleach concentrates having high alkalinity | |
US2413495A (en) | Phosphoric acid detergent | |
CN107574445A (en) | A kind of environment-friendly type copper material cleaning agent | |
US5286403A (en) | Concentrated cleaning compositions | |
US3626559A (en) | Process of shaping metal surfaces and cleaning the same | |
US5250230A (en) | Composition and process for cleaning metals | |
US3010907A (en) | Alkaline cleaning compositions | |
US4029607A (en) | Drain cleaning compositions | |
PT715646E (en) | TENSOTIVE | |
US2593259A (en) | Acid cleaner and detergent | |
US2155046A (en) | Inhibited detergent composition | |
US4087387A (en) | Foam cleaning composition |