US2215814A - Radiator cleaning composition and method - Google Patents
Radiator cleaning composition and method Download PDFInfo
- Publication number
- US2215814A US2215814A US182797A US18279737A US2215814A US 2215814 A US2215814 A US 2215814A US 182797 A US182797 A US 182797A US 18279737 A US18279737 A US 18279737A US 2215814 A US2215814 A US 2215814A
- Authority
- US
- United States
- Prior art keywords
- sodium
- alkali
- metal
- radiator
- hexametaphosphate
- 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
Classifications
-
- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/02—Inorganic compounds
- C11D7/04—Water-soluble compounds
- C11D7/10—Salts
- C11D7/16—Phosphates including polyphosphates
-
- 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0073—Anticorrosion compositions
-
- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/02—Inorganic compounds
- C11D7/04—Water-soluble compounds
- C11D7/10—Salts
-
- 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
- C23G1/14—Cleaning or pickling metallic material with solutions or molten salts with alkaline solutions
- C23G1/16—Cleaning or pickling metallic material with solutions or molten salts with alkaline solutions using inhibitors
- C23G1/18—Organic inhibitors
Definitions
- This invention relates to a radiator cleaning composition and method for preventing the formation of and removing the deposits in automobile radiators and the passages in the engine block. It relates more particularly to a radiator cleaning composition containing an alkalimetal hexametaphosphate such, for example, as sodium hexametaphosphate or an alkali-metal tripolyphosphate such, for example, as sodium tripolyphosphate as an essential ingredient.
- an alkalimetal hexametaphosphate such, for example, as sodium hexametaphosphate or an alkali-metal tripolyphosphate such, for example, as sodium tripolyphosphate as an essential ingredient.
- a temporarily hard water that is, a water containing calcium and/or magnesium bicarbonates
- the bicarbonates are converted, upon heating the water, into the corresponding carbonates which form deposits on the radiator and the cooling passages in the engine block.
- permanently hard water that is, water containing calcium and/ or magnesium sulphates in solution
- it will, upon heating, attack the iron or other metal forming oxidized products or iron rust.
- the deposits are likely to contain grease, core sand, dirt, deposits from the water and deposits resulting from the use of certain anti-freeze compounds. Some or all of these deposits may be present and hinder the proper functioning of the cooling system.
- My radiator cleaning composition contains as an essential ingredient an alkali-metal hexametaphosphate such, for example, as sodium hexample, as a tannin body, an alkali-metal sulphite,
- the alkali-metal hexametaphosphates or tripolyphosphates for example sodium hexametaphosphate or sodium tripolyphosphate, have the property, when added to water containing calcium and/or magnesium, of sequestering the calcium and magnesium and forming therewith very 5 slightly ionized soluble complexes, thereby preventing the precipitation of these metals.
- This property of alkali-metal hexametaphosphates and tripolyphosphates by which they can sequester the calcium in slightly ionized condition not only enables them to prevent the precipitation of calcium and magnesium, but imparts to water so treated the property of dissolving or peptizing any calcareous deposits which have al ready formed.
- the alkali-metal hexametaphosphates and tripolyphosphates have therefore a solvent effect on any deposits by virtue of their efiect in maintaining the water continuously unsaturated with respect to these deposits.
- This solvent efiect on the calcareous deposits loosens the deposits and any corrosion products intermixed therewith and enables the other ingredients of the radiator cleaning composition to more effectively attack other deposits such as dirt and grease which may be embedded in the calcareous deposits.
- My composition preferably contains a water soluble afil'al i in addition to the alkali-metal h'exa'rnetaphosphate o'r''tripolyphosphate.
- Any suftable alkali maybe employed, for example, among others, trisodium phosphate, sodium carbonate, borax, modified soda (a mixture of sodium carbonate and sodium bicarbonate or caustic soda), sodium silicate, sodium bicarbonate, sodium orthoand metasilicates, sodium metaborate, sodium normal pyrophosphate, and sodium hydroxide.
- the corresponding salts of other alkali-metals may be used in place of the sodium salts.
- the preferred alkalis are trisodium phosphate, sodium carbonate, sodium orthosilicate and sodium metasilicate.
- the silicates in addition to being good alkalis, exercise an inhibitive influence on corrosion of soft metals such as aluminum cylinder heads.
- the preferred alkalis as well as some of the othersmen tioned, act asfirfiering agents to prevent too great acidity or alkalinity in the water solution of the radiator cleaning composition, thereby maintainin g the solut i9 1' 1 a t a pl l value Wis most efiecfive for preventing corrosion or for preventing the formation of scale or for causing dissolutigj of scale which has already been formed.
- the alkali in my composition protects the metal against corrosion and acts as a saponifying, detergent and peptizing agent on any grease 252. cowosmows.
- Tannins may be used in my composition either in place of or in addition to the alkali.
- suitable tannins I mention quebracho extract, cutch and logwood, although other tannins or similar materials may be employed. These materials are referred to herein as tannin bodies, the term being intended to include not only the tannins, pseudo tannins or alginates, but also other compounds having similar properties.
- These tannin bodies like trisodium phosphate and sodium carbonate and other bufiering salts, act as buffering agents to prevent too great acidity or alkalinity in the water, and also act as dispersive agents on calcium precipitates such as calcium phosphate.
- the tannin bodies are capable of holding in colloidal solution a considerable amount of precipitated hardness.
- the tannin bodies absorb oxygen, thereby decreasing the tendency of the metal to corrode.
- Alkali-metal sulphites for example, sodium sulphite, also have the property of absorbing oxygen and may be used in place of or in addition to the tannin bodies.
- I may use 2 oz. of sodium hexametaphosphate or sodium tripolyphosphate or a mixture thereof, 1 oz. of trisodium phosphate, and /2 oz. of sodium sulphite.
- I may use 2 oz. of sodium hexametaphosphate or sodium tripolyphosphate, 1 oz. of sodium carbonate, and /2 oz. of sodium sulphite.
- I may use in place of the sodium sulphite in either of these examples the same amount, namely, oz., of a tannin body such as quebracho extract.
- a further example is 2 oz. sodium hexametaphosphate, 2% oz. sodium metasilicate, and 2 oz. of quebracho extract.
- the composition may contain an alkali, this may be omitted where the composition is to be used simply to fiush out the radiator and engine jacket so as to remove the scale. as contrasted with being kept in the radiator for long periods of time in order to prevent the formation of scale. Where the composition is to remain in the radiator for long periods of time, there is a tendency for the hexametaphosphate or tripolyphosphate to revert to the nr'rhnnhosphate. Enough algali may be used in the composition to offset any undesirableaci'd':
- the corrosion inhibitors may likewise be omitted where the composition is to be used merely for flushing out the radiator and will not remain in the system for a long period of time.
- alkali-metal chromates or bichromates such, for example, as sodium chromate or sodium bichromate. These materials act as b'ufiering agents to prevent too great acidity or alkalinity in the water and, in addition, have the property of forming films on iron which protect it against corrosion.
- Inhibitors such as quinoline and substituted quinolines, such as quinoline ethiodide, or other coal-tar derivatives and acid sludges from the washing of petroleum and coal-tar distillation products, such as are used in the pickling of iron and steel, may also be employed in my composition, these inhibitors having the property in case too great activity develops of preventing attack on the metal, but allowing the solution to i f- V06 attack and dissolve the rust.
- These materials are, in general, basic nitrogen compounds of high molecular weight.
- nitrogen base inhibitor to designate these inhibitors with the intent that it will include not only the aliphatic amines, such as n-tributyl, n-diamyl amine, n-triamyl amine, Wtnearomm amines, such as aniline, pyidi n e or guinoline, etc., but also the complex fitrogen base sludges formed in the acid washing oTfietroleum and coal-tar distillation products. "The proportions of the various ingredients may be varied widely according to the type of deposit which it is desired to dissolve or prevent. The quantities given in the examples are suitable for use in a radiator having a capacity of gal. where it is desired to simply maintain the radiator clean. If, however, it is desired to dissolve a deposit which has already formed, or if the radiator has a greater capacity than that given, the amount of composition should be increased.
- aliphatic amines such as n-tributyl, n-diamyl amine,
- the alkali-metal hexametaphosphate which I prefer to use is in the soluble sodium hexametaphosphate sometimes called Grahams salt.
- the sodium hexametaphosphate is assumed to be a complex of the general formula Naz(Na4PeOia), although some authorities believe that salts of the formulas Na5(NaPsO1a) and N8.4(N9.2P601s) may also be present.
- Sodium hexametaphosphate in readily soluble glassy form may be prepared by strongly heating monosodium dihydrogen orthophosphate and rapidly cooling the molten mass.
- the alkali-metal tripolyphosphates are chemical compounds of the formula MsPaOm in their anhydrous form, in which M represents an alkalimetal.
- Sodium tripolyphosphate is the most common and important of the alkali-metal tripolyphosphates. Chemical and X-ray analyses show that sodium tripolyphosphate is a definite chemical compound which is distinct from both sodium hexametaphosphate and sodium pyrophosphate and that it is not a mixture of the two.
- Sodium tripolyphosphate is fusible and may be solidified by very rapidly cooling in a glassy amorphous form. Under slower coolingit solidifies in the form of crystals. The glass may be converted into crystal form by annealing. So-
- dium tripolyphosphate forms a crystalline hydrate of the general formula NaaPzomfiHzO.
- Sodium tripolyphosphate is colorless, appearing white in the granulated crystalline form. When crushed it forms a free-flowing granular mass. By suitable precautions it may be produced in a mass which readily disintegrates into its constituent fine crystals.
- Sodium tripolyphosphate is not deliquescent and particularly in its hydrated form may be preserved indefinitely in ordinary atmospheres without caking or picking up moisture.
- Sodium tripolyphosphate is readily water-soluble in both its glassy and crystalline forms.
- the alkali-metal metaphosphates and tripolyphosphates are molecularly dehydrated phosphates as such term is employed in Hall and Jackson Patent No. 1,903,041.
- sodium metaphosphate (NaPOa) may be considered as derived from monosodium dihydrogen orthophosphate by the removal of water of constitution.
- sodium tripolyphosphate may be similarly considered as derived by molecular dehydration of a mixture of orthophosphates which is intermediate in acidity between the monosodium dihydrogen orthophosphate and the disodium monohydrogen orthophosphate.
- the metaphosphates and tripolyphosphates may be regarded as salts of condensed or molecularly dehydrated phosphoric acids which have been molecularly dehydrated to a greater extent than pyrophosphoric acid.
- Sodium tripolyphosphate has several advantages over sodium hexamethaphosphate in a radiator cleaning composition.
- Sodium tripolyphosphate is not hygroscopic, as is sodium hexametaphosphate. Particularly in its hydrated form, sodium tripolyphosphate may be preserved indefinitely in ordinary atmospheres without caking or picking up moisture. Furthermore, it is much more stable in highly heated alkaline solutions than sodium hexametaphosphate and therefore does not revert to the orthophosphate form nearly as rapidly as the hexametaphosphate. Also, it is not necessary, in making sodium tripolyphosphate, to resort to the drastic chilling which is required in producing the glassy sodium hexametaphosphate.
- a radiator cleaning composition containing effective amounts of an alkali-metal hexametaphosphate and a water-soluble alkali.
- a radiator cleaning composition containing effective amounts of an alkali-metal hexametaphosphate, a water-soluble alkali, and a corrosion inhibitor of the group consisting of a tannin body, an alkali-metal sulphite, an alkali-metal chromate, and an alkali-metal bichromate.
- a method of cleaning automobile radiators which comprises treating the surfaces having ferruginous and calcareous deposits thereon with an aqueous solution containing effective amounts of an alkali-metal hexametaphosphate and a water-soluble alkali, whereby the deposits are dissolved without material injury to the treated surfaces.
- a method of cleaning automobile radiators which comprises treating the surfaces having ferruginous and calcareous deposits thereon with an aqueous solution containing an effective amount of an alkali-metal hexametaphosphate, a watersoluble alkali, and a corrosion inhibitor of the group consisting of a tannin body, an alkalimetal sulphite, an alkali-metal chromate, and an alkali-metal bichromate.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- Inorganic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Detergent Compositions (AREA)
Description
252. COWS Patented Sept. 24, 1940 UNITED STATES PATENT OFFICE RADIATOR CLEANING COMPOSITION AND METHOD Ralph E. Hall, Mount Lebanon, Pa., assignor to Hall Laboratories, Inc., Pittsburgh, Pa., a corporation of Pennsylvania No Drawing. Application December 31, 1937, Serial No. 182,797
4 Claims. (01. 252-439) This invention relates to a radiator cleaning composition and method for preventing the formation of and removing the deposits in automobile radiators and the passages in the engine block. It relates more particularly to a radiator cleaning composition containing an alkalimetal hexametaphosphate such, for example, as sodium hexametaphosphate or an alkali-metal tripolyphosphate such, for example, as sodium tripolyphosphate as an essential ingredient.
The present application is a continuation-inpart of my copending application Serial No. 721,314, filed April 19, 1934.
If a temporarily hard water is used in a radiator, that is, a water containing calcium and/or magnesium bicarbonates, the bicarbonates are converted, upon heating the water, into the corresponding carbonates which form deposits on the radiator and the cooling passages in the engine block. If permanently hard water, that is, water containing calcium and/ or magnesium sulphates in solution, is used, it will, upon heating, attack the iron or other metal forming oxidized products or iron rust.
The majority of natural waters contain both temporary hardness and permanent hardness and may therefore cause either scale or corrosion, or both. Even though the water contains permanent hardness only, scale may be deposited by the vaporization of water in the radiator and its continuous replenishment with more water. The water in the radiator will eventually become saturated with calcium sulphate and deposit scale, particularly on the heated surfaces of the cylinder block. Corrosion may also occur with a water containing no permanent hardness.
In addition to the deposits of calcium and/or magnesium, and the oxide of the metals, the deposits are likely to contain grease, core sand, dirt, deposits from the water and deposits resulting from the use of certain anti-freeze compounds. Some or all of these deposits may be present and hinder the proper functioning of the cooling system.
My radiator cleaning composition contains as an essential ingredient an alkali-metal hexametaphosphate such, for example, as sodium hexample, as a tannin body, an alkali-metal sulphite,
or an alkali-metal chromate or bichromate.
The alkali-metal hexametaphosphates or tripolyphosphates, for example sodium hexametaphosphate or sodium tripolyphosphate, have the property, when added to water containing calcium and/or magnesium, of sequestering the calcium and magnesium and forming therewith very 5 slightly ionized soluble complexes, thereby preventing the precipitation of these metals. This property of alkali-metal hexametaphosphates and tripolyphosphates by which they can sequester the calcium in slightly ionized condition not only enables them to prevent the precipitation of calcium and magnesium, but imparts to water so treated the property of dissolving or peptizing any calcareous deposits which have al ready formed. The alkali-metal hexametaphosphates and tripolyphosphates have therefore a solvent effect on any deposits by virtue of their efiect in maintaining the water continuously unsaturated with respect to these deposits. This solvent efiect on the calcareous deposits loosens the deposits and any corrosion products intermixed therewith and enables the other ingredients of the radiator cleaning composition to more effectively attack other deposits such as dirt and grease which may be embedded in the calcareous deposits.
My composition preferably contains a water soluble afil'al i in addition to the alkali-metal h'exa'rnetaphosphate o'r''tripolyphosphate. Any suftable alkali maybe employed, for example, among others, trisodium phosphate, sodium carbonate, borax, modified soda (a mixture of sodium carbonate and sodium bicarbonate or caustic soda), sodium silicate, sodium bicarbonate, sodium orthoand metasilicates, sodium metaborate, sodium normal pyrophosphate, and sodium hydroxide. The corresponding salts of other alkali-metals may be used in place of the sodium salts. The preferred alkalis are trisodium phosphate, sodium carbonate, sodium orthosilicate and sodium metasilicate. The silicates, in addition to being good alkalis, exercise an inhibitive influence on corrosion of soft metals such as aluminum cylinder heads. The preferred alkalis as well as some of the othersmen tioned, act asfirfiering agents to prevent too great acidity or alkalinity in the water solution of the radiator cleaning composition, thereby maintainin g the solut i9 1' 1 a t a pl l value Wis most efiecfive for preventing corrosion or for preventing the formation of scale or for causing dissolutigj of scale which has already been formed.
The alkali in my composition protects the metal against corrosion and acts as a saponifying, detergent and peptizing agent on any grease 252. cowosmows.
or oil which may be present. It also acts as a peptizing and detergent agent on iron rust and clay and other dirt which may form mud.
Tannins, pseudo tannin, alginates and similar compounds, may be used in my composition either in place of or in addition to the alkali. As suitable tannins, I mention quebracho extract, cutch and logwood, although other tannins or similar materials may be employed. These materials are referred to herein as tannin bodies, the term being intended to include not only the tannins, pseudo tannins or alginates, but also other compounds having similar properties. These tannin bodies, like trisodium phosphate and sodium carbonate and other bufiering salts, act as buffering agents to prevent too great acidity or alkalinity in the water, and also act as dispersive agents on calcium precipitates such as calcium phosphate. The tannin bodies are capable of holding in colloidal solution a considerable amount of precipitated hardness. In addition, the tannin bodies absorb oxygen, thereby decreasing the tendency of the metal to corrode. Alkali-metal sulphites, for example, sodium sulphite, also have the property of absorbing oxygen and may be used in place of or in addition to the tannin bodies.
As a specific example of my composition, I may use 2 oz. of sodium hexametaphosphate or sodium tripolyphosphate or a mixture thereof, 1 oz. of trisodium phosphate, and /2 oz. of sodium sulphite. As another example, I may use 2 oz. of sodium hexametaphosphate or sodium tripolyphosphate, 1 oz. of sodium carbonate, and /2 oz. of sodium sulphite. I may use in place of the sodium sulphite in either of these examples the same amount, namely, oz., of a tannin body such as quebracho extract. A further example is 2 oz. sodium hexametaphosphate, 2% oz. sodium metasilicate, and 2 oz. of quebracho extract.
Although it is preferred that the composition contain an alkali, this may be omitted where the composition is to be used simply to fiush out the radiator and engine jacket so as to remove the scale. as contrasted with being kept in the radiator for long periods of time in order to prevent the formation of scale. Where the composition is to remain in the radiator for long periods of time, there is a tendency for the hexametaphosphate or tripolyphosphate to revert to the nr'rhnnhosphate. Enough algali may be used in the composition to offset any undesirableaci'd':
ity developed by the reversion of the hexametaphosphate or tripolyphosphate. The corrosion inhibitors may likewise be omitted where the composition is to be used merely for flushing out the radiator and will not remain in the system for a long period of time.
I may also use in my composition alkali-metal chromates or bichromates such, for example, as sodium chromate or sodium bichromate. These materials act as b'ufiering agents to prevent too great acidity or alkalinity in the water and, in addition, have the property of forming films on iron which protect it against corrosion.
Inhibitors such as quinoline and substituted quinolines, such as quinoline ethiodide, or other coal-tar derivatives and acid sludges from the washing of petroleum and coal-tar distillation products, such as are used in the pickling of iron and steel, may also be employed in my composition, these inhibitors having the property in case too great activity develops of preventing attack on the metal, but allowing the solution to i f- V06 attack and dissolve the rust. These materials are, in general, basic nitrogen compounds of high molecular weight. For simplicity, I shall use the term nitrogen base inhibitor to designate these inhibitors with the intent that it will include not only the aliphatic amines, such as n-tributyl, n-diamyl amine, n-triamyl amine, Wtnearomm amines, such as aniline, pyidi n e or guinoline, etc., but also the complex fitrogen base sludges formed in the acid washing oTfietroleum and coal-tar distillation products. "The proportions of the various ingredients may be varied widely according to the type of deposit which it is desired to dissolve or prevent. The quantities given in the examples are suitable for use in a radiator having a capacity of gal. where it is desired to simply maintain the radiator clean. If, however, it is desired to dissolve a deposit which has already formed, or if the radiator has a greater capacity than that given, the amount of composition should be increased.
The alkali-metal hexametaphosphate which I prefer to use is in the soluble sodium hexametaphosphate sometimes called Grahams salt. The sodium hexametaphosphate is assumed to be a complex of the general formula Naz(Na4PeOia), although some authorities believe that salts of the formulas Na5(NaPsO1a) and N8.4(N9.2P601s) may also be present. Sodium hexametaphosphate in readily soluble glassy form may be prepared by strongly heating monosodium dihydrogen orthophosphate and rapidly cooling the molten mass.
The alkali-metal tripolyphosphates are chemical compounds of the formula MsPaOm in their anhydrous form, in which M represents an alkalimetal. Sodium tripolyphosphate is the most common and important of the alkali-metal tripolyphosphates. Chemical and X-ray analyses show that sodium tripolyphosphate is a definite chemical compound which is distinct from both sodium hexametaphosphate and sodium pyrophosphate and that it is not a mixture of the two. Sodium tripolyphosphate is fusible and may be solidified by very rapidly cooling in a glassy amorphous form. Under slower coolingit solidifies in the form of crystals. The glass may be converted into crystal form by annealing. So-
dium tripolyphosphate forms a crystalline hydrate of the general formula NaaPzomfiHzO. Sodium tripolyphosphate is colorless, appearing white in the granulated crystalline form. When crushed it forms a free-flowing granular mass. By suitable precautions it may be produced in a mass which readily disintegrates into its constituent fine crystals. Sodium tripolyphosphate is not deliquescent and particularly in its hydrated form may be preserved indefinitely in ordinary atmospheres without caking or picking up moisture. Sodium tripolyphosphate is readily water-soluble in both its glassy and crystalline forms.
The alkali-metal metaphosphates and tripolyphosphates are molecularly dehydrated phosphates as such term is employed in Hall and Jackson Patent No. 1,903,041. For example, sodium metaphosphate (NaPOa) may be considered as derived from monosodium dihydrogen orthophosphate by the removal of water of constitution. Likewise, sodium tripolyphosphate may be similarly considered as derived by molecular dehydration of a mixture of orthophosphates which is intermediate in acidity between the monosodium dihydrogen orthophosphate and the disodium monohydrogen orthophosphate. The metaphosphates and tripolyphosphates may be regarded as salts of condensed or molecularly dehydrated phosphoric acids which have been molecularly dehydrated to a greater extent than pyrophosphoric acid.
Sodium tripolyphosphate has several advantages over sodium hexamethaphosphate in a radiator cleaning composition. Sodium tripolyphosphate is not hygroscopic, as is sodium hexametaphosphate. Particularly in its hydrated form, sodium tripolyphosphate may be preserved indefinitely in ordinary atmospheres without caking or picking up moisture. Furthermore, it is much more stable in highly heated alkaline solutions than sodium hexametaphosphate and therefore does not revert to the orthophosphate form nearly as rapidly as the hexametaphosphate. Also, it is not necessary, in making sodium tripolyphosphate, to resort to the drastic chilling which is required in producing the glassy sodium hexametaphosphate.
While I prefer to use sodium hexametaphosphate or tripolyphosphate, the corresponding salts of the other alkali-metals such as those of potassium, lithium and ammonium may be used.
I have specifically described certain preferred embodiments of my invention. It is to be understood, however, that the invention is not limited to the preferred examples which have been given by way of illustration only, but that the invention may be otherwise embodied or practiced within the scope of the following claims.
I claim:
1. A radiator cleaning composition containing effective amounts of an alkali-metal hexametaphosphate and a water-soluble alkali.
2. A radiator cleaning composition containing effective amounts of an alkali-metal hexametaphosphate, a water-soluble alkali, and a corrosion inhibitor of the group consisting of a tannin body, an alkali-metal sulphite, an alkali-metal chromate, and an alkali-metal bichromate.
3. A method of cleaning automobile radiators which comprises treating the surfaces having ferruginous and calcareous deposits thereon with an aqueous solution containing effective amounts of an alkali-metal hexametaphosphate and a water-soluble alkali, whereby the deposits are dissolved without material injury to the treated surfaces.
4. A method of cleaning automobile radiators which comprises treating the surfaces having ferruginous and calcareous deposits thereon with an aqueous solution containing an effective amount of an alkali-metal hexametaphosphate, a watersoluble alkali, and a corrosion inhibitor of the group consisting of a tannin body, an alkalimetal sulphite, an alkali-metal chromate, and an alkali-metal bichromate.
' RALPH E. HALL.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US182797A US2215814A (en) | 1937-12-31 | 1937-12-31 | Radiator cleaning composition and method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US182797A US2215814A (en) | 1937-12-31 | 1937-12-31 | Radiator cleaning composition and method |
Publications (1)
Publication Number | Publication Date |
---|---|
US2215814A true US2215814A (en) | 1940-09-24 |
Family
ID=22670080
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US182797A Expired - Lifetime US2215814A (en) | 1937-12-31 | 1937-12-31 | Radiator cleaning composition and method |
Country Status (1)
Country | Link |
---|---|
US (1) | US2215814A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2458292A (en) * | 1945-01-02 | 1949-01-04 | Hall Lab Inc | Method of retarding the reversion of alkali-metal phosphate glass in aqueous solutions and a composition of matter thereof |
US2503381A (en) * | 1948-11-26 | 1950-04-11 | Arrow Lab Inc | Detergent composition |
US2509440A (en) * | 1950-05-30 | Caustic alkali detergent | ||
US2673144A (en) * | 1950-06-10 | 1954-03-23 | Standard Oil Co | Auxiliary alcohol-water fuel |
US2802788A (en) * | 1957-08-13 | Cleaning composition for automotive | ||
DE967894C (en) * | 1942-11-01 | 1957-12-27 | Benckiser Gmbh Joh A | Detergents and detergents for automatic dishwashers |
US2901437A (en) * | 1955-05-03 | 1959-08-25 | Wright Chem Corp | Corrosion inhibiting composition |
US3375200A (en) * | 1965-08-17 | 1968-03-26 | Nalco Chemical Co | Cooling water treatment and compositions useful therein |
US3652422A (en) * | 1970-08-05 | 1972-03-28 | Agnes M Hughes | Cleaner for wigs |
US4094701A (en) * | 1976-03-18 | 1978-06-13 | Oxy Metal Industries Corporation | Method for cleaning tin surfaces |
FR2501357A1 (en) * | 1981-03-04 | 1982-09-10 | Permo | Water treatment to de-foul heat exchanger - involves using additives to remove deposits, suspend particles, inhibit corrosion and/or improve filterability |
-
1937
- 1937-12-31 US US182797A patent/US2215814A/en not_active Expired - Lifetime
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2509440A (en) * | 1950-05-30 | Caustic alkali detergent | ||
US2802788A (en) * | 1957-08-13 | Cleaning composition for automotive | ||
DE967894C (en) * | 1942-11-01 | 1957-12-27 | Benckiser Gmbh Joh A | Detergents and detergents for automatic dishwashers |
US2458292A (en) * | 1945-01-02 | 1949-01-04 | Hall Lab Inc | Method of retarding the reversion of alkali-metal phosphate glass in aqueous solutions and a composition of matter thereof |
US2503381A (en) * | 1948-11-26 | 1950-04-11 | Arrow Lab Inc | Detergent composition |
US2673144A (en) * | 1950-06-10 | 1954-03-23 | Standard Oil Co | Auxiliary alcohol-water fuel |
US2901437A (en) * | 1955-05-03 | 1959-08-25 | Wright Chem Corp | Corrosion inhibiting composition |
US3375200A (en) * | 1965-08-17 | 1968-03-26 | Nalco Chemical Co | Cooling water treatment and compositions useful therein |
US3652422A (en) * | 1970-08-05 | 1972-03-28 | Agnes M Hughes | Cleaner for wigs |
US4094701A (en) * | 1976-03-18 | 1978-06-13 | Oxy Metal Industries Corporation | Method for cleaning tin surfaces |
FR2501357A1 (en) * | 1981-03-04 | 1982-09-10 | Permo | Water treatment to de-foul heat exchanger - involves using additives to remove deposits, suspend particles, inhibit corrosion and/or improve filterability |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2215814A (en) | Radiator cleaning composition and method | |
US2191199A (en) | Abrasive detergent composition | |
US4606890A (en) | Process for conditioning metal surfaces | |
US2980620A (en) | Method of inhibiting ice melting salts and products for use in ice melting | |
US5183590A (en) | Corrosion inhibitors | |
US4202796A (en) | Anti-corrosion composition | |
US3959167A (en) | Method and composition of inhibiting scale | |
JPS58177479A (en) | Method of controlling corrosion and sedimentation in aqueous system and composition therefor | |
US2802788A (en) | Cleaning composition for automotive | |
JPS6039171A (en) | Metal pretreatment composition | |
JPS58199878A (en) | Method and composition for inhibiting corrosion and sedimentation in aqueous system | |
CA2884086C (en) | Methods and compositions to prevent caking of sodium chloride and prevent transition metal stains | |
US3099521A (en) | Water treatment | |
US2374100A (en) | Water treatment | |
NZ242457A (en) | Carbon steel corrosion inhibiting compositions for use in potable water systems; method of reducing the solubilisation of soluble lead from lead-containing components of potable water systems | |
AU667310B2 (en) | Naphthylamine polycarboxylic acids | |
US5171477A (en) | Corrosion inhibition in chelant solutions | |
JPS5891174A (en) | Rust preventive material for brine of inorganic salt | |
US3589858A (en) | Inhibiting the corrosion of metals in a water system | |
US3518203A (en) | Corrosion and scale inhibitor compositions and processes therefor | |
US3451939A (en) | Threshold compositions and methods | |
US3910854A (en) | Combustion chamber cleaning and corrosion preventing agent | |
US5401311A (en) | Method for removing deposits from cooling water systems | |
JPS5925977A (en) | Composition for metal surface corrosion prevention | |
US4229409A (en) | Method of inhibiting corrosion of aluminum with 2-phosphono-butane-1,2,4-tricarboxylic acid |