US3173875A - Acid bowl cleaner - Google Patents
Acid bowl cleaner Download PDFInfo
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- US3173875A US3173875A US152131A US15213161A US3173875A US 3173875 A US3173875 A US 3173875A US 152131 A US152131 A US 152131A US 15213161 A US15213161 A US 15213161A US 3173875 A US3173875 A US 3173875A
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- acid
- weight percent
- ferrous
- compositions
- chloride
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- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 title claims description 51
- 239000002253 acid Substances 0.000 title claims description 41
- 239000000203 mixture Substances 0.000 claims description 87
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 59
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 claims description 37
- 229960002089 ferrous chloride Drugs 0.000 claims description 33
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 claims description 32
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 29
- OBMBUODDCOAJQP-UHFFFAOYSA-N 2-chloro-4-phenylquinoline Chemical compound C=12C=CC=CC2=NC(Cl)=CC=1C1=CC=CC=C1 OBMBUODDCOAJQP-UHFFFAOYSA-N 0.000 claims description 19
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims description 18
- 239000011790 ferrous sulphate Substances 0.000 claims description 17
- 235000003891 ferrous sulphate Nutrition 0.000 claims description 17
- 229910000359 iron(II) sulfate Inorganic materials 0.000 claims description 17
- 229910002651 NO3 Inorganic materials 0.000 claims description 13
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 13
- 239000011260 aqueous acid Substances 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 35
- 235000011007 phosphoric acid Nutrition 0.000 description 30
- 235000011167 hydrochloric acid Nutrition 0.000 description 24
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 22
- 239000007864 aqueous solution Substances 0.000 description 17
- 238000000034 method Methods 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 229910052742 iron Inorganic materials 0.000 description 11
- 238000004140 cleaning Methods 0.000 description 10
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- 229910052573 porcelain Inorganic materials 0.000 description 8
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 7
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 7
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 6
- 230000002378 acidificating effect Effects 0.000 description 5
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 4
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 4
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 4
- 239000003945 anionic surfactant Substances 0.000 description 4
- 239000003599 detergent Substances 0.000 description 4
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000001119 stannous chloride Substances 0.000 description 4
- 235000011150 stannous chloride Nutrition 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 235000002906 tartaric acid Nutrition 0.000 description 4
- 239000011975 tartaric acid Substances 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 230000002238 attenuated effect Effects 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 238000010186 staining Methods 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 239000010408 film Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 231100001261 hazardous Toxicity 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 229910000619 316 stainless steel Inorganic materials 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
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 240000004922 Vigna radiata Species 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229940074323 antara Drugs 0.000 description 1
- 238000005284 basis set Methods 0.000 description 1
- MWOBKFYERIDQSZ-UHFFFAOYSA-N benzene;sodium Chemical compound [Na].C1=CC=CC=C1 MWOBKFYERIDQSZ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006196 drop Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- YMTINGFKWWXKFG-UHFFFAOYSA-N fenofibrate Chemical compound C1=CC(OC(C)(C)C(=O)OC(C)C)=CC=C1C(=O)C1=CC=C(Cl)C=C1 YMTINGFKWWXKFG-UHFFFAOYSA-N 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 159000000014 iron salts Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- -1 polyoxyethylene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- FBWNMEQMRUMQSO-UHFFFAOYSA-N tergitol NP-9 Chemical compound CCCCCCCCCC1=CC=C(OCCOCCOCCOCCOCCOCCOCCOCCOCCO)C=C1 FBWNMEQMRUMQSO-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
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
- C11D7/08—Acids
Definitions
- This invention relates, in general, to acid detergent compositions. More particularly, it pertains to attenuated acid compositions particularly adapted for removing stains from porcelain-type fixtures.
- Porcelain fixtures such as those customarily found in lavatories are readily susceptible to iron staining where the water conveyed to and drained from the fixture has an initial high iron content and where the water solubilizes iron in lower valence state from iron conduits leading into the fixtures.
- the problem of iron staining is particularly acute when, after draining the water, a thin film of water remains on the porcelain fixture. Upon evaporation of this film, iron salts remain which are readily converted to the higher valence state. It is this form of the iron which adheres so tenaciously to the fixture and which is, therefore, responsible for the unsightly and undesirable iron stains.
- cleaners containing sodium bisulfate as the active ingredient depend on the release of a strong acid for stain removal properties, there are, therefore, certain precautions and restrictions in their use. This type of cleaning compound should not be employed on metal or enamel fixtures. It should not be allowed to contact the skin and, in addition, inhalation of the cleaner dust should be avoided.
- Acidic cleaning compositions based on muriatic acid and particularly adapted for use at institutional-type facilities such as public carrier terminals and industrial plants generally contain about 20 to 23 weight percent of hydrogen chloride. These compositions are, in general, subject to the same precautions and restrictions as previously set forth for sodium bisulfate.
- acidic cleaning compositions based upon either hydrochloric acid or sodium bisulfate, at the concentrations noted above, are effective for removing stains from porcelain-type fixtures, they are, however, particularly hazardous to handle.
- an object of the invention to provide acid detergent compositions which are relatively safe and easy to handle. Another object of the invention is to provide attenuated acid cleaners for removing stains from porcelain-type fixtures which are as effective as the hazardous-to-handle acid compositions of the prior art. A further object of the invention is to provide a process for removing stains from porcelain-type fixtures wherein the cleaning compositions employed in the process are as effective as the acid compositions of the prior art but are not as hazardous to handle.
- a sgluble ferrou s salt isaddedtoan acid selected from the group consisting of phosphorig cid, hydrochl o ric a c id and mixttge giereof, it surprisingly and unexpectedly incEases the rate atwhich the acid removes stains from porcelain-type fixtures.
- a mild acid such as phosphoric acid when employed in combination with a soluble ferrous salt will remove stains at a faster rate than, for example, a 20 weight percent aqueous solution of hydrochloric acid.
- less concentrated solutions of hydrochloric acid can be employed in combination with a soluble ferrous salt and these attenuated combinations remove stain at a faster rate than the 20 weight percent hydrochloric acid compositions of the prior art.
- composition disclosed by McGaughey for removing iron oxide deposits from glass molds was evaluated for its capacity to remove iron stains from porcelain fixtures.
- a comparative study was made in order to ascertain the effectiveness of certain of the compositions of the invention when employed at the concentration disclosed by McGaughey.
- the composition of the invention employed was an aqueous solution of phosphoric acid and ferrous chloride. Comparative studies were also carried out at 10 weight percent acid concentration and 2 and 32 weight percent reducing agent concentration, respectively.
- the procedure employed for evaluating stain removal properties was somewhat similar to that described in Federal Specification P-P-00586, Revision 1, August 24, 1 955. Briefly, the staining procedure consisted of applying a 5% ferric chloride solution on an unglazed porcelain plate and setting the stain by baking for two hours at C. The plate was cooled and a drop of the stain removal solution to be tested was applied thereto. The rate of stain removal was determined by measuring the time necessary to remove all of the stain in the area covered by the test drop.
- compositions are set forth in Table A below.
- M represents the composition disclosed by McGaughey and X represents the composition of the invention previously defined.
- X represents the composition of the invention previously defined.
- the compositions are compared on the preferred weight basis set forth in the McGaughey disclosure.
- weight percent of the acid has been employed and 2 and 32 weight percent of the reducing agent has been used, respectively.
- an aqueous solution of 10 weight percent phosphoric acid was employed as the stain removal agent. In each instance, the quantities are expressed on a weight percent basis.
- ferrous chloride ferrous sulfate, ferrous nitrate and mixtures thereof.
- the concentrations described above give good results, it is preferred, however, in order to obtain a better balance of properties to employ an acid detergent composition comprising about 5 to weight percent a 32 weight percent reducing agent concentration, the composition of the invention is more than 100 times as effective as the composition disclosed by McGaughey.
- the Me- Gaughey disclosure at the various concentrations set forth, does not remove stain as fast as an aqueous solution of 10 weight percent phosphoric acid.
- compositions of the invention comprise an aqueous solution of a water-soluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate, and mixtures thereof in combination with an acid selected from the group consisting of hydrochloric acid, phosphoric acid, and mixtures thereof.
- a water-soluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate, and mixtures thereof in combination with an acid selected from the group consisting of hydrochloric acid, phosphoric acid, and mixtures thereof.
- the ingredients of the composition can be varied over a wide range and still maintain the advantages of the invention.
- the acid detergent composition of this invention should contain at least about 0.2 weight percent of an acid selected from the group consisting of phosphoric acid, hydrochloric acid and mixtures thereof and at least about 0.5 weight percent of a water-soluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate and mixtures thereof. While any amounts of ferrous salt and of acid above the minimums recited are effective and produce the desired results of this invention, it is desirable, due to the cost of the acids and ferrous salts, to use the minimum amount necessary for the particular cleaning job. In this connection, consideration must be given to solubility limitations.
- the acid detergent composition of this invention generally comprises an aqueous solution of about 0.2 to 30 weight percent of an acid selected from the group consisting of phosphoric acid, hydrochloric acid and mixtures thereof and about 0.5 to 38 weight percent of a water-soluble ferrous salt se- Table A
- an acid selected from the group consisting of phosphoric acid, hydrochloric acid and mixtures thereof and about 0.5 to 38 weight percent of a water-soluble ferrous salt se- Table A
- a B o M X M X M x Tartarie Acid 0.2 10.0 10.0
- compositions of phosphoric acid and about 6 to 30 weight percent of of the invention are from about 8 to about times 25 the water-soluble ferrous salt or about 6 to 20 weight more effective for removing iron stains from a porcelain percent hydrochloric acid and about 1 to 24 weight perplate than a similar composition based on the Mccent of the water-soluble ferrous salt.
- the composition of the invention is about 8 improved properties.
- the compositions have the same proportions illustrated under heading C, when the compositions are as set forth above except that up to 75 weight percent compared at a 10 weight percent acid concentration and 35 of the acid can be phosphoric acid.
- the soluble ferrous salts which can be employed to accelerate the rate at which the mineral acids remove stain and deposit from porcelain-type fixtures consist of ferrous chloride, ferrous sulfate and ferrous nitrate. Mixtures of these ferrous salts are also suitable i the compositions of the invention. A mixture of soluble ferrous salts is particularly desirable, however, when the compositions of the invention are prepared in stainless steel equipment. Thus, it has been found that when the acid composition is formulated with ferrous chloride alone, the formulated composition has a tendency to corrode the steel equipment used for its preparation. However, when the acid composition is formulated with a mixture of ferrous chloride and ferrous sulfate, the corrosiveness of the composition towards stainless steel is significantly minimized or completely eliminated.
- a preferred composition for such application is an aqueous solution of about 18 to 22 weight percent of phosphoric acid, about 2 to 6 weight percent of ferrous chloride and about 6 to 10 weight percent of ferrous sulfate. No problem of corrosion is encountered, however, when rubher-lined equipment is employed to prepare the acid compositions of the invention.
- a preferred bowl cleaning composition which is particularly adapted for sale in the industrial and domestic market is an aqueous solution of about 5 to 25 Weight percent of phosphoric acid, about 6 to 30 weight percent of a water-soluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate and mixture thereof, about 10 weight percent of isopropanol and about 0.5 weight percent of an alkyl benzene sodium sulfonate wherein the alkyl group contains from about 10 to 15 carbon atoms.
- EXAMPLE I Table I 1101 9 2O 36 I1 0 91 90 8O 64 Destaining time, See 300 345 45 1 EXAMPLE II
- Ferrous chloride was added to aqueous solutions of hydrochloric acid and drops of the resulting compositions were applied to test plates stained in accordance with the procedure outlined above and the stain removal rates were determined.
- the concentrations of hydrogen chloride and ferrous chloride in each solution and stain removal rates are set forth in Table II below. It will be noted from the table that ferrous chloride significantly increases the rate at each aqueous solutions of hydrochloric acid remove stain from porcelain surfaces.
- This example is significant because it demonstrates that a mild acid, in this instance phosphoric acid, to which has been added ferrous chlo ride, is as effective as the more concentrated and hazardtent of the corrosion of these compositions was determined by immersing a 316 stainless steel panel in the stain removal solution for four hours at 95 F.
- the surfactant employed was a liquid nonionic dispersant marketed by the Antara Division of the General Aniline and Film Corporation under the trade designation Igepal CO-630.
- anionic type surfactants can also be employed with the compositions of the invention.
- the alkylarylsulfonates are illustrative of the anionic surfactants which can be used. Since the latter type surfactants tend to be incompatible with the acid system, a coupling agent such as isopropanol is employed to prevent phase separation of the anionic surfactant from the acidulous portion of the composition.
- EXAMPLE VI This example illustrates a preferred bowl cleaning composition particularly adaptcd for sale in the industrial and domestic market.
- the acid and soluble ferrous salts are formulated with an anionic surfactant, a non-ionic surfactant and perfume.
- the concentration of the components of this composition are set forth in Table VI.
- Nonyl plionoxy polyoxyothylene ethanol wherein the molecule contains, by weight. 65% polyoxyethylene and is prepared by condensing 9-10 mols of ethylene oxide with 1 mol of nonyl phenol.
- this composition In addition to having highly effective stain removal properties, this composition also has germicidal properties. Thus, this composition was tested using the AOAC Method against M.p.v. aureus at C. In th1s test the endpoint for phenol was at a dilution of 1 to 60, which is the most acceptable figure for this organism. The composition had a phenol coeflicient of 2.11.
- EXAMPLE VII Ferrous chloride is added to an aqueous solution of hydrochloric acid and phosphoric acid and drops of the resulting compositions are applied to plates stained in accordance with the procedure previously outlined. The concentration of the ingredients of each solution and the stain removal rates are set forth in Table VII below.
- An aqueous acid detergent solution of about 0.2 to 30 weight percent of an acid selected from the group consisting of phosphoric acid, hydrochloric acid and mixtures thereof and about 0.5 to 38 Weight percent of a watersoluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate and mixtures thereof.
- An aqueous acid detergent solution of about 6 to 20 weight percent of hydrochloric acid and about 1 to 24 weight percent of a water-soluble ferrous salt selected from the group consistingof ferrous chloride, ferrous sulfate, ferrous nitrate and mixtures thereof.
- An aqueous acid detergent solution of about 18 to 22 weight percent of phosphoric acid, about 2 to 6 weight percent of ferrous chloride and about 6 to 10 weight percent of ferrous sulfate.
- a process for removing iron stains from porcelaintype fixtures which comprises contacting said stains with an aqueous acid detergent solution, withdrawing said detergent solution and rinsing with water, said detergent solution comprising at least about 0.2% of an acid selected from the group consisting of phosphoric acid, hydrochloric acid and mixtures thereof and at least about 0.5 weight percent of a water-soluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate and mixtures thereof.
- a process for removing iron stains from porcelaintype fixtures which comprises contacting said stains with an aqueous acid detergent solution, withdrawing said detergent solution and rinsing with water, said detergent solution comprising about 0.2 to 30 Weight percent of an acid selected from the group consisting of phosphoric acid, hydrochloric acid and mixtures thereof and 0.5 to 38 weight percent of a water-soluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate and mixtures thereof.
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
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Description
a United States Patent Ofifice 3,173,875 Patented Mar. 16, 1965 Michigan No Drawing. Filed Nov. 9, 1961, Ser. No. 152,131
12 Claims. (Cl. 252--105) This invention relates, in general, to acid detergent compositions. More particularly, it pertains to attenuated acid compositions particularly adapted for removing stains from porcelain-type fixtures.
Porcelain fixtures such as those customarily found in lavatories are readily susceptible to iron staining where the water conveyed to and drained from the fixture has an initial high iron content and where the water solubilizes iron in lower valence state from iron conduits leading into the fixtures. The problem of iron staining is particularly acute when, after draining the water, a thin film of water remains on the porcelain fixture. Upon evaporation of this film, iron salts remain which are readily converted to the higher valence state. It is this form of the iron which adheres so tenaciously to the fixture and which is, therefore, responsible for the unsightly and undesirable iron stains.
It has been customary to employ acidic compositions to remove these stains. Thus, cleaning compositions based upon hydrochloric acid or sodium bisulfate are well known in the art. Sodium bisulfate, also known as niter cake, depends for its stain removal action on the formation of sulfuric acid on contact with water. The Federal specification for bowl cleaners issued by the General Services Administration, OC-42 6D, August 19, 1957, is based upon sodium hydrogen sulfate. This specification requires that, upon analysis by titration of a suitable solution, the material must have a sulfuric acid equivalent of not less than 30 weight percent.
Since cleaners containing sodium bisulfate as the active ingredient depend on the release of a strong acid for stain removal properties, there are, therefore, certain precautions and restrictions in their use. This type of cleaning compound should not be employed on metal or enamel fixtures. It should not be allowed to contact the skin and, in addition, inhalation of the cleaner dust should be avoided.
A review of bowl cleaning compositions based upon sodium hydrogen sulfate is set forth in an article by Milton A. Lesser entitled Washroom Sanitation Specialties, Soap and Sanitary Chemicals, page 139, October 1947.
Acidic cleaning compositions based on muriatic acid and particularly adapted for use at institutional-type facilities such as public carrier terminals and industrial plants generally contain about 20 to 23 weight percent of hydrogen chloride. These compositions are, in general, subject to the same precautions and restrictions as previously set forth for sodium bisulfate.
Although acidic cleaning compositions based upon either hydrochloric acid or sodium bisulfate, at the concentrations noted above, are effective for removing stains from porcelain-type fixtures, they are, however, particularly hazardous to handle.
Therefore, it is an object of the invention to provide acid detergent compositions which are relatively safe and easy to handle. Another object of the invention is to provide attenuated acid cleaners for removing stains from porcelain-type fixtures which are as effective as the hazardous-to-handle acid compositions of the prior art. A further object of the invention is to provide a process for removing stains from porcelain-type fixtures wherein the cleaning compositions employed in the process are as effective as the acid compositions of the prior art but are not as hazardous to handle.
In accordance with the invention, it has been discovered that when a sgluble ferrou s salt isaddedtoan acid selected from the group consisting of phosphorig cid, hydrochl o ric a c id and mixttge giereof, it surprisingly and unexpectedly incEases the rate atwhich the acid removes stains from porcelain-type fixtures. Thus, a mild acid such as phosphoric acid when employed in combination with a soluble ferrous salt will remove stains at a faster rate than, for example, a 20 weight percent aqueous solution of hydrochloric acid. In addition, and in accordance with the invention, less concentrated solutions of hydrochloric acid can be employed in combination with a soluble ferrous salt and these attenuated combinations remove stain at a faster rate than the 20 weight percent hydrochloric acid compositions of the prior art.
The prior art discloses that stannous chloride solutions acidulated with tartaric acid can be employed to remove iron oxide and carbonaceous deposits from the interior of glass molds. Thus, US. 2,116,034, McGaughey, discloses that five pounds of stannous chloride and one gallon of water, which water has been acidulated with ounce of tartaric acid, provides a composition for reducing the iron oxide deposits on the interior surface of such molds. McGaughey points out that only enough of the tartaric acid is used to give the water and acidic characteristic and that the tartaric acid is necessary for producing a suitable solvent for the stannous chloride.
The composition disclosed by McGaughey for removing iron oxide deposits from glass molds was evaluated for its capacity to remove iron stains from porcelain fixtures. In addition, a comparative study was made in order to ascertain the effectiveness of certain of the compositions of the invention when employed at the concentration disclosed by McGaughey. The composition of the invention employed was an aqueous solution of phosphoric acid and ferrous chloride. Comparative studies were also carried out at 10 weight percent acid concentration and 2 and 32 weight percent reducing agent concentration, respectively.
The procedure employed for evaluating stain removal properties was somewhat similar to that described in Federal Specification P-P-00586, Revision 1, August 24, 1 955. Briefly, the staining procedure consisted of applying a 5% ferric chloride solution on an unglazed porcelain plate and setting the stain by baking for two hours at C. The plate was cooled and a drop of the stain removal solution to be tested was applied thereto. The rate of stain removal was determined by measuring the time necessary to remove all of the stain in the area covered by the test drop.
The composition, concentration and rate of stain removal are set forth in Table A below. In this table, M represents the composition disclosed by McGaughey and X represents the composition of the invention previously defined. Under the heading A, the compositions are compared on the preferred weight basis set forth in the McGaughey disclosure. Under the headings B and C,
weight percent of the acid has been employed and 2 and 32 weight percent of the reducing agent has been used, respectively. Under the heading D, an aqueous solution of 10 weight percent phosphoric acid was employed as the stain removal agent. In each instance, the quantities are expressed on a weight percent basis.
iected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate and mixtures thereof.
Although the concentrations described above give good results, it is preferred, however, in order to obtain a better balance of properties to employ an acid detergent composition comprising about 5 to weight percent a 32 weight percent reducing agent concentration, the composition of the invention is more than 100 times as effective as the composition disclosed by McGaughey. In addition, it will be noted from the table that the Me- Gaughey disclosure, at the various concentrations set forth, does not remove stain as fast as an aqueous solution of 10 weight percent phosphoric acid.
The compositions of the invention comprise an aqueous solution of a water-soluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate, and mixtures thereof in combination with an acid selected from the group consisting of hydrochloric acid, phosphoric acid, and mixtures thereof. The ingredients of the composition can be varied over a wide range and still maintain the advantages of the invention. However, the acid detergent composition of this invention should contain at least about 0.2 weight percent of an acid selected from the group consisting of phosphoric acid, hydrochloric acid and mixtures thereof and at least about 0.5 weight percent of a water-soluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate and mixtures thereof. While any amounts of ferrous salt and of acid above the minimums recited are effective and produce the desired results of this invention, it is desirable, due to the cost of the acids and ferrous salts, to use the minimum amount necessary for the particular cleaning job. In this connection, consideration must be given to solubility limitations. In general, amounts of acid in excess of 30 weight percent and amounts of ferrous salt in excess of 38 weight percent are insoluble in the aqueous solution and, thus, such excess amounts do nothing to increase the effectiveness of the solution. Accordingly, it is not desirable to use such excess amounts of acid and ferrous salt although solutions containing such excess amounts are effective. Thus, the acid detergent composition of this invention generally comprises an aqueous solution of about 0.2 to 30 weight percent of an acid selected from the group consisting of phosphoric acid, hydrochloric acid and mixtures thereof and about 0.5 to 38 weight percent of a water-soluble ferrous salt se- Table A A B o M X M X M x Tartarie Acid 0.2 10.0 10.0 Stannous Chloride 37.5 2.0 32.0 Phosphoric Acid 0. 2 10. 0 10. 0 10. 0 Ferrous Chloride 37. 2.0 32. Water 62.3 62.3 88.0 88.0 58.0 58.0 90.0
Stain removal rate, See 1,610 190 2,650 55 680 6 670 $402. 5lbs.
It will be noted from the table that the compositions of phosphoric acid and about 6 to 30 weight percent of of the invention are from about 8 to about times 25 the water-soluble ferrous salt or about 6 to 20 weight more effective for removing iron stains from a porcelain percent hydrochloric acid and about 1 to 24 weight perplate than a similar composition based on the Mccent of the water-soluble ferrous salt.
'Gaughey disclosure. Thus, as illustrated under head- Mixtures of hydrochloric acid and phosphoric acid can ing A, when the compositions are compared on the also be formulated with a soluble ferrous salt in order same weight basis as set forth in the McGaughey 30 to provide an acid cleaning composition of significantly disclosure, the composition of the invention is about 8 improved properties. When a mixture of the acids is times more effective for removing stain. However, as employed, the compositions have the same proportions illustrated under heading C, when the compositions are as set forth above except that up to 75 weight percent compared at a 10 weight percent acid concentration and 35 of the acid can be phosphoric acid.
The soluble ferrous salts which can be employed to accelerate the rate at which the mineral acids remove stain and deposit from porcelain-type fixtures consist of ferrous chloride, ferrous sulfate and ferrous nitrate. Mixtures of these ferrous salts are also suitable i the compositions of the invention. A mixture of soluble ferrous salts is particularly desirable, however, when the compositions of the invention are prepared in stainless steel equipment. Thus, it has been found that when the acid composition is formulated with ferrous chloride alone, the formulated composition has a tendency to corrode the steel equipment used for its preparation. However, when the acid composition is formulated with a mixture of ferrous chloride and ferrous sulfate, the corrosiveness of the composition towards stainless steel is significantly minimized or completely eliminated. A preferred composition for such application is an aqueous solution of about 18 to 22 weight percent of phosphoric acid, about 2 to 6 weight percent of ferrous chloride and about 6 to 10 weight percent of ferrous sulfate. No problem of corrosion is encountered, however, when rubher-lined equipment is employed to prepare the acid compositions of the invention.
A preferred bowl cleaning composition which is particularly adapted for sale in the industrial and domestic market is an aqueous solution of about 5 to 25 Weight percent of phosphoric acid, about 6 to 30 weight percent of a water-soluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate and mixture thereof, about 10 weight percent of isopropanol and about 0.5 weight percent of an alkyl benzene sodium sulfonate wherein the alkyl group contains from about 10 to 15 carbon atoms.
In order to further illustrate the invention and its accompanying advantages, the following specific examples are presented.
The procedure employed in each of the examples was, unless otherwise stated, to prepare a 5% solution of ferric chloride from anhydrous ferric chloride of A.C.S. grade. The ferric chloride solution was then applied to one side of an unglazed porcelain streak plate and the stain was.
set by baking the plate for two hours at 130 C. The plate was cooled and a drop of the solution being evaluated for stain removal properties was applied thereto. The rate of stain removal was determined by measuring the time necessary to remove all the stain in the area covered by the test drop. In each instance, the concentration is set forth in weight percent.
EXAMPLE I Table I 1101 9 2O 36 I1 0 91 90 8O 64 Destaining time, See 300 345 45 1 EXAMPLE II Ferrous chloride was added to aqueous solutions of hydrochloric acid and drops of the resulting compositions were applied to test plates stained in accordance with the procedure outlined above and the stain removal rates were determined. The concentrations of hydrogen chloride and ferrous chloride in each solution and stain removal rates are set forth in Table II below. It will be noted from the table that ferrous chloride significantly increases the rate at each aqueous solutions of hydrochloric acid remove stain from porcelain surfaces. Of most significance, however, is the discovery that an aqueous solution of 9 weight percent hydrogen chloride and 6.3 weight percent ferrous chloride (10 weight percent FeCl -4H O) is as etfective as a 20 weight percent solution of hydrochloric acid. Thus, a less concentrated acid can be used to achieve results which formerly required a more concentrated form of the acid.
A drop of each solution was ous-to-handle hydrochloric acid of the prior art for removing stains from porcelain surfaces.
Table III H3PO4..- 1 5 10 20 Calculated FeClg 38.0 25.4 25.4 25.4
Destaining time, See 12 90 50 20 EXAMPLE IV Aqueous solutions of ferrous chloride were applied to test plates stained in accordance with the procedure previously outlined in order to determine the effectiveness of ferrous chloride, per se. The concentration of the ferrous chloride solutions and the rate of stain removal are set forth in Table IV below. It will be noted from the table that at the end of one hour the stains had not been removed.
Table IV FeC-h-4H 0 15 30 11:0 85 40 Calculated FeCl 9. 5 19.0 38.0 Destuining time, See... 3, 600 3, 600 3, 600
EXAMPLE V Ferrous chloride, ferrous sulfate, a surfactant and perfume were added to aqueous solutions of phosphoric acid and drops of the resulting compositions were applied to plates stained in accordance with the procedure previously outlined, except that the test plates were baked for three hours instead of two hours. The concentration of the ingredients of each solution and the average stain removal rate for each composition are set forth in Table V below. This example illustrates stain removal compositions which can be prepared in stainless steel Table II Calculated FeCl 38.0 6.3 25.4 12.7 0.6 6.3 12.7 25.4 6.3 0.6
Dest-Jniuig time, Sec- 90 155 35 10 45 20 10 l 15 EXAMPLE HI equipment without corroding that equipment. The ex- Ferrous chloride was added to aqueous solutions of phosphoric acid and the resulting compositions were applied to test plates stained in accordance with the pro cedure previously described and the rates of stain removal were measured. The concentration of phosphoric acid and ferrous chloride in each solution and stain removal rates are set forth in Table III below. It will be noted from the table that an aqueous solution of 10 weight percent phosphoric acid to which has been added 25.4 weight percent ferrous chloride (40 weight percent FeCl -4H O) is about as effective as a 20 percent solution of hydrochloric acid. This example is significant because it demonstrates that a mild acid, in this instance phosphoric acid, to which has been added ferrous chlo ride, is as effective as the more concentrated and hazardtent of the corrosion of these compositions was determined by immersing a 316 stainless steel panel in the stain removal solution for four hours at 95 F. The surfactant employed was a liquid nonionic dispersant marketed by the Antara Division of the General Aniline and Film Corporation under the trade designation Igepal CO-630. In addition to the nonionic surfactants, anionic type surfactants can also be employed with the compositions of the invention. The alkylarylsulfonates are illustrative of the anionic surfactants which can be used. Since the latter type surfactants tend to be incompatible with the acid system, a coupling agent such as isopropanol is employed to prevent phase separation of the anionic surfactant from the acidulous portion of the composition.
EXAMPLE VI This example illustrates a preferred bowl cleaning composition particularly adaptcd for sale in the industrial and domestic market. In this composition, the acid and soluble ferrous salts are formulated with an anionic surfactant, a non-ionic surfactant and perfume. The concentration of the components of this composition are set forth in Table VI.
Table VI H PO (75%) 23.90 FeCl (34.5%) 10.40 FeSO -7H O 13.10 Nonionic surfactant 1 0.35
Perfume 0.05
Isopropanol 10.00 Anionic surfactant 2 0.50 H O 41.70
1 Nonyl plionoxy polyoxyothylene ethanol wherein the molecule contains, by weight. 65% polyoxyethylene and is prepared by condensing 9-10 mols of ethylene oxide with 1 mol of nonyl phenol.
-Alk vl benzene sodium sultonate wherein the alkyl group contains from 10-15 carbon atoms.
In addition to having highly effective stain removal properties, this composition also has germicidal properties. Thus, this composition was tested using the AOAC Method against M.p.v. aureus at C. In th1s test the endpoint for phenol was at a dilution of 1 to 60, which is the most acceptable figure for this organism. The composition had a phenol coeflicient of 2.11.
EXAMPLE VII Ferrous chloride is added to an aqueous solution of hydrochloric acid and phosphoric acid and drops of the resulting compositions are applied to plates stained in accordance with the procedure previously outlined. The concentration of the ingredients of each solution and the stain removal rates are set forth in Table VII below.
Table VII Dcstaining time, See 20 1-5 minutes. The acid detergent composition is then withdrawn and the area is rinsed with water. When more persistent stains are encountered, it will be necessary, of course, to contact the stains with the acidic compositions of the invention for a longer period of time. The exact time will be readily apparent, however, to those having ordinary skill in this art.
This application is a continuation-in-part of our copending application Serial No. 731,192, filed April 28, 1958, now abandoned.
It will be understood that various changes, modifications and alterations may be made in the instant invention without departing from the spirit and scope thereof and as such the invention is not to be limited except by the appended claims.
We claim:
1. An aqueous acid detergent solution of at least about 0.2 weight percent of an acid selected from the group consisting of phosphoric acid. hydrochloric acid and mixtures thereof and at least about 0.5 weight percent of a water-soluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate and mixtures thereof.
2. The acid detergent solution of claim 1 wherein the acid is phosphoric acid.
3. The acid detergent solution of claim 1 wherein the acid is hydrochloric acid.
4. The acid detergent solution of claim 1 wherein the ferrous salt is ferrous chloride.
5. An aqueous acid detergent solution of about 0.2 to 30 weight percent of an acid selected from the group consisting of phosphoric acid, hydrochloric acid and mixtures thereof and about 0.5 to 38 Weight percent of a watersoluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate and mixtures thereof.
6. An acid detergent solution in accordance with claim 5 wherein said acid is a mixture of hydrochloric and phosphoric acids and up to about weight percent of said acid is phosphoric acid.
7. An aqueous acid detergent solution of about 5 to 25 weight percent of phosphoric acid and about 6 to 30 weight percent of a water-soluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate and mixtures thereof.
8. An aqueous acid detergent solution of about 6 to 20 weight percent of hydrochloric acid and about 1 to 24 weight percent of a water-soluble ferrous salt selected from the group consistingof ferrous chloride, ferrous sulfate, ferrous nitrate and mixtures thereof.
9. An aqueous acid detergent solution of about 18 to 22 weight percent of phosphoric acid, about 2 to 6 weight percent of ferrous chloride and about 6 to 10 weight percent of ferrous sulfate.
10. An aqueous acid detergent solution of about 5 to 25 weight percent of phosphoric acid, about 6 to 30 weight percent of a water-soluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate and mixtures thereof, about 10 weight percent of isopropanol and about 0.5 weight percent of an alkyl benzene sodium sulfonate wherein the alkyl group contains from about 10 to 15 carbon atoms.
11. A process for removing iron stains from porcelaintype fixtures which comprises contacting said stains with an aqueous acid detergent solution, withdrawing said detergent solution and rinsing with water, said detergent solution comprising at least about 0.2% of an acid selected from the group consisting of phosphoric acid, hydrochloric acid and mixtures thereof and at least about 0.5 weight percent of a water-soluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate and mixtures thereof.
12. A process for removing iron stains from porcelaintype fixtures which comprises contacting said stains with an aqueous acid detergent solution, withdrawing said detergent solution and rinsing with water, said detergent solution comprising about 0.2 to 30 Weight percent of an acid selected from the group consisting of phosphoric acid, hydrochloric acid and mixtures thereof and 0.5 to 38 weight percent of a water-soluble ferrous salt selected from the group consisting of ferrous chloride, ferrous sulfate, ferrous nitrate and mixtures thereof.
References Cited in the file of this patent UNITED STATES PATENTS 10 Phair Nov. 4, 1924 McGaughey May 3, 1938 Halpern Nov. 14, 1950 Chester et al. Oct. 2, 1951 McDonald et al. Apr. 6, 1954 FOREIGN PATENTS Australia Nov. 16, 1955 OTHER REFERENCES Uses and Applications of Chemicals and Related Materials" by Gregory, Reinhold Publ. Co. (1939), p. 288.
Claims (1)
- 5. AN AQUEOUS ACID DETERGENT SOLUTION OF ABOUT 0.2 TO 30 WEIGHT PERCENT OF AN ACID SELECTED FROM THE GROUP CONSISTING OF PHOSPHORIC ACID, HYDROCHLORIC ACID AND MIXTURES THEREOF AND ABOUT 0.5 TO 38 WEIGHT PERCENT OF A WATERSOLUBLE FEROUS SALT SELECTED FROM THE GROUP CONSISTING OF FERROUS CHLORIDE, FERROUS SULFATE, FERROUS NITRATE AND MIXTURES THEREOF.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US152131A US3173875A (en) | 1961-11-09 | 1961-11-09 | Acid bowl cleaner |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US152131A US3173875A (en) | 1961-11-09 | 1961-11-09 | Acid bowl cleaner |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3173875A true US3173875A (en) | 1965-03-16 |
Family
ID=22541635
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US152131A Expired - Lifetime US3173875A (en) | 1961-11-09 | 1961-11-09 | Acid bowl cleaner |
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| US (1) | US3173875A (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3538008A (en) * | 1968-09-13 | 1970-11-03 | Madison Chem Corp | Cleaning of sewers and drains |
| US3897357A (en) * | 1972-12-06 | 1975-07-29 | American Home Prod | Bacteriostatic toilet bowl cleaner compositions |
| US3969258A (en) * | 1974-10-10 | 1976-07-13 | Pennwalt Corporation | Low foaming acid-anionic surfactant sanitizer compositions |
| US4032466A (en) * | 1976-04-16 | 1977-06-28 | Basf Wyandotte Corporation | Acid cleaner and process for disposal thereof |
| FR2392106A1 (en) * | 1977-05-25 | 1978-12-22 | Basf Wyandotte Corp | THICK ACID CLEANING PRODUCT |
| US4324678A (en) * | 1979-11-23 | 1982-04-13 | Howson Barry R | Method of cleaning fibreglass |
| US4412932A (en) * | 1979-11-23 | 1983-11-01 | Howson Barry R | Method of cleaning fibreglass |
| US4666625A (en) * | 1984-11-27 | 1987-05-19 | The Drackett Company | Method of cleaning clogged drains |
| US4828743A (en) * | 1987-11-20 | 1989-05-09 | Boyle-Midway Household Products, Inc. | Composition for rust removal and method of use thereof |
| US20050196442A1 (en) * | 2004-03-05 | 2005-09-08 | Huang Hai Y. | Polymeric compositions and dosage forms comprising the same |
| US20080153734A1 (en) * | 2006-12-22 | 2008-06-26 | Shenzhen Futaihong Precision Industry Co., Ltd. | Metal surface cleaner and method for cleaning metal parts |
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| US1321182A (en) * | 1919-11-11 | Picklino-bath | ||
| US1503450A (en) * | 1923-09-07 | 1924-07-29 | Kuykendall William | Cleaning compound |
| US1514067A (en) * | 1923-06-16 | 1924-11-04 | Kohnstamm & Co Inc H | Souring composition and method |
| US2116634A (en) * | 1934-08-08 | 1938-05-10 | Lyons Delia | Process of making rolled oats cereal flakes |
| US2529549A (en) * | 1947-06-30 | 1950-11-14 | Irving A Halpern | Method of cleaning cement surfaces preparatory to painting |
| US2569453A (en) * | 1949-09-14 | 1951-10-02 | Poor & Co | Vitreous enamel base stock, vitreous enameled articles and method |
| US2674523A (en) * | 1953-04-24 | 1954-04-06 | Kelite Products Inc | Process and composition for treatment of magnesium prior to spot welding |
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| US1321182A (en) * | 1919-11-11 | Picklino-bath | ||
| US1514067A (en) * | 1923-06-16 | 1924-11-04 | Kohnstamm & Co Inc H | Souring composition and method |
| US1503450A (en) * | 1923-09-07 | 1924-07-29 | Kuykendall William | Cleaning compound |
| US2116634A (en) * | 1934-08-08 | 1938-05-10 | Lyons Delia | Process of making rolled oats cereal flakes |
| US2529549A (en) * | 1947-06-30 | 1950-11-14 | Irving A Halpern | Method of cleaning cement surfaces preparatory to painting |
| US2569453A (en) * | 1949-09-14 | 1951-10-02 | Poor & Co | Vitreous enamel base stock, vitreous enameled articles and method |
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Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3538008A (en) * | 1968-09-13 | 1970-11-03 | Madison Chem Corp | Cleaning of sewers and drains |
| US3897357A (en) * | 1972-12-06 | 1975-07-29 | American Home Prod | Bacteriostatic toilet bowl cleaner compositions |
| US3969258A (en) * | 1974-10-10 | 1976-07-13 | Pennwalt Corporation | Low foaming acid-anionic surfactant sanitizer compositions |
| US4032466A (en) * | 1976-04-16 | 1977-06-28 | Basf Wyandotte Corporation | Acid cleaner and process for disposal thereof |
| FR2392106A1 (en) * | 1977-05-25 | 1978-12-22 | Basf Wyandotte Corp | THICK ACID CLEANING PRODUCT |
| US4324678A (en) * | 1979-11-23 | 1982-04-13 | Howson Barry R | Method of cleaning fibreglass |
| US4412932A (en) * | 1979-11-23 | 1983-11-01 | Howson Barry R | Method of cleaning fibreglass |
| US4666625A (en) * | 1984-11-27 | 1987-05-19 | The Drackett Company | Method of cleaning clogged drains |
| US4828743A (en) * | 1987-11-20 | 1989-05-09 | Boyle-Midway Household Products, Inc. | Composition for rust removal and method of use thereof |
| US20050196442A1 (en) * | 2004-03-05 | 2005-09-08 | Huang Hai Y. | Polymeric compositions and dosage forms comprising the same |
| US20080153734A1 (en) * | 2006-12-22 | 2008-06-26 | Shenzhen Futaihong Precision Industry Co., Ltd. | Metal surface cleaner and method for cleaning metal parts |
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