US20110006264A1 - Corrosion inhibitor - Google Patents

Corrosion inhibitor Download PDF

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Publication number
US20110006264A1
US20110006264A1 US12/677,467 US67746708A US2011006264A1 US 20110006264 A1 US20110006264 A1 US 20110006264A1 US 67746708 A US67746708 A US 67746708A US 2011006264 A1 US2011006264 A1 US 2011006264A1
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Prior art keywords
acid
glycerol
triol
diol
corrosion
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Abandoned
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US12/677,467
Inventor
Bernt O. Myrvold
Kristin Sandersen Gretland
Tom Stylo
Rune Buvarp
Bente Seljebakken Klausen
Guro Elise Fredheim
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Borregaard AS
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Borregaard Industries Ltd
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Assigned to BORREGAARD INDUSTRIES LIMITED NORGE reassignment BORREGAARD INDUSTRIES LIMITED NORGE ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KLAUSEN, BENTE SELJEBAKKEN, STYLO, TOM, GRETLAND, KRISTIN SANDERSEN, BUVARP, RUNE, FREDHEIM, GURO ELISE, MYRVOLD, BERNT O.
Publication of US20110006264A1 publication Critical patent/US20110006264A1/en
Assigned to BORREGAARD AS reassignment BORREGAARD AS ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BORREGAARD INDUSTRIES LIMITED NORGE
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    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/08Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
    • C23F11/10Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
    • C23F11/12Oxygen-containing compounds
    • C23F11/122Alcohols; Aldehydes; Ketones
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/68Treatment of water, waste water, or sewage by addition of specified substances, e.g. trace elements, for ameliorating potable water
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/04Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in markedly acid liquids
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/08Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
    • C23F11/10Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2103/00Nature of the water, waste water, sewage or sludge to be treated
    • C02F2103/16Nature of the water, waste water, sewage or sludge to be treated from metallurgical processes, i.e. from the production, refining or treatment of metals, e.g. galvanic wastes
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2103/00Nature of the water, waste water, sewage or sludge to be treated
    • C02F2103/20Nature of the water, waste water, sewage or sludge to be treated from animal husbandry
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2103/00Nature of the water, waste water, sewage or sludge to be treated
    • C02F2103/22Nature of the water, waste water, sewage or sludge to be treated from the processing of animals, e.g. poultry, fish, or parts thereof
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2103/00Nature of the water, waste water, sewage or sludge to be treated
    • C02F2103/22Nature of the water, waste water, sewage or sludge to be treated from the processing of animals, e.g. poultry, fish, or parts thereof
    • C02F2103/24Nature of the water, waste water, sewage or sludge to be treated from the processing of animals, e.g. poultry, fish, or parts thereof from tanneries
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2103/00Nature of the water, waste water, sewage or sludge to be treated
    • C02F2103/26Nature of the water, waste water, sewage or sludge to be treated from the processing of plants or parts thereof
    • C02F2103/28Nature of the water, waste water, sewage or sludge to be treated from the processing of plants or parts thereof from the paper or cellulose industry
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2103/00Nature of the water, waste water, sewage or sludge to be treated
    • C02F2103/32Nature of the water, waste water, sewage or sludge to be treated from the food or foodstuff industry, e.g. brewery waste waters
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2303/00Specific treatment goals
    • C02F2303/04Disinfection
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2303/00Specific treatment goals
    • C02F2303/08Corrosion inhibition

Definitions

  • the present invention concerns the discovery that a diol or triol or as mixture thereof provides a corrosion-reducing or inhibiting effect when added to acids or acid containing compositions used in metal or metallic equipment in production factories or plants for reducing or inhibiting microbial growth.
  • Such factories or plants may be factories or plants for silage of grass, ensilage of fish and/or fish products, continued treatment/ensilage of slaughterhouse waste and food waste or in drinking facilities for farm house animals such as poultry or pigs.
  • Tanneries, metallurgic industry and pulp mills are other examples of factories or plants where large amounts of acids are used.
  • Organic acids have many beneficial effects when it comes to controlling microbial growth. They are thus frequently used for the preservation of organic materials. Propionic acid is used as a grain preservative, for silage of grass and as a feed additive. Formic acid is used in ensilage of fish, slaughterhouse waste, food waste and grass, and also in pig and chicken feed. Acetic acid is used for conservation of fish. Benzoic acid is used for fish ensilage. Other acids, or mixture of acids, are also used. Organic acids are also used in the drinking water for pigs and poultry, among others. The addition of organic acids to compound feed for pigs, sheep, goats, poultry, cattle, horses, dogs, cats and fur-bearing animals has an efficacious effect on their growth and health. Further, the acid addition to compound feed reduces the amount of consumed compound feed per kg of growth without the increased growth affecting the quality of the meat. This reduces feed cost by reducing the feeding period and promoting better housing utilization.
  • Strong acids like sulfuric acid, sulfurous acid and hydrochloric acids are used in many processes. Tanning, metallurgy and pulping are just a few examples.
  • diol any organic compound with at two hydroxyl group, e.g. ethylene glycol or propylene glycol.
  • triol is meant any organic compound with three hydroxyl groups, e.g. glycerol.
  • Diols and triols can be produced by fermentation, by hydrolysis or by trans-esterification.
  • Glycerol is produced in large quantities from the saponification of fats and the trans-esterification of fats to fatty acid methyl esters during biodiesel production.
  • the diol or triol is added in quantities from 10 to 90% of the final mixture with the acids, preferably from 40 to 60%.
  • FR 2 391 261A
  • the advantages of simple diols and triols are several. They are cheaper. They are liquid at room temperature, and thus easier to use in any formulation. With the use of a diol like glycol or the triol glycerol we are not using scarce food resources as chemical raw materials.
  • Glycerol has been shown to reduce skin corrosion in a formic acid that has been partly neutralised with ammonia (NO 307 591 B). We here show that diols or triols also function as a corrosion inhibitor for metals without any neutralisation of the acids.
  • Carbon steel coupons C1018 were used for the corrosion tests.
  • the coupons were sonicated in acetone for 10 minutes, then dried in a heating cabinet, cooled in a desiccator and weighed. They were hung in polypropylene strips inside the test bottles filled with acid and the added corrosion inhibitor. The bottles were sealed with plastic film to prevent evaporation of the acid. The test bottles were placed on magnetic stirrers to prevent diffusion gradients within the solution. After 3 days the steel coupons were removed form the bottles and washed with warm water and acetone before they were dried in a heating cabinet, cooled in a desiccator and weighed. All experiments were done in duplicate and the average corrosion rates are given.
  • glycerol is at least as effective as the commercially used lignosulfonates.
  • glycerol is at least as effective as the commerically used lignosulfonates.
  • glycerol is effective for several mineral acids and organic acids.

Abstract

It has surprisingly been discovered that simple diols and triols work as corrosion inhibitors in concentrated organic and inorganic acids, e.g. used as additives in metallic equipment in factories and plants. These corrosion inhibitors are cheap and readily available in large quantities. The diol and triol also reduces evaporation of the acid, and thus improves the working environment.

Description

  • The present invention concerns the discovery that a diol or triol or as mixture thereof provides a corrosion-reducing or inhibiting effect when added to acids or acid containing compositions used in metal or metallic equipment in production factories or plants for reducing or inhibiting microbial growth. Such factories or plants may be factories or plants for silage of grass, ensilage of fish and/or fish products, continued treatment/ensilage of slaughterhouse waste and food waste or in drinking facilities for farm house animals such as poultry or pigs. Tanneries, metallurgic industry and pulp mills are other examples of factories or plants where large amounts of acids are used.
  • Organic acids have many beneficial effects when it comes to controlling microbial growth. They are thus frequently used for the preservation of organic materials. Propionic acid is used as a grain preservative, for silage of grass and as a feed additive. Formic acid is used in ensilage of fish, slaughterhouse waste, food waste and grass, and also in pig and chicken feed. Acetic acid is used for conservation of fish. Benzoic acid is used for fish ensilage. Other acids, or mixture of acids, are also used. Organic acids are also used in the drinking water for pigs and poultry, among others. The addition of organic acids to compound feed for pigs, sheep, goats, poultry, cattle, horses, dogs, cats and fur-bearing animals has an efficacious effect on their growth and health. Further, the acid addition to compound feed reduces the amount of consumed compound feed per kg of growth without the increased growth affecting the quality of the meat. This reduces feed cost by reducing the feeding period and promoting better housing utilization.
  • Strong acids like sulfuric acid, sulfurous acid and hydrochloric acids are used in many processes. Tanning, metallurgy and pulping are just a few examples.
  • There are a number of problems, however, with using acids, and in particular strong acids such as formic acid or mineral acids, including the corrosion of the equipment. Acids are corrosive and yearly corrosion from handling these acids costs millions of dollar. There is considerable corrosion on storage tanks, pipes, valves and the mixing equipment in the production line for pelleted feed in particular. This drives up the operating costs and leads to the added burden of increased maintenance and system monitoring.
  • There are also problems with using volatile for those handling the product. Formic acid is particularly corrosive to skin and can cause damage from etching, which is why it full body protection is needed. As an example during pelleting process the temperature rises to 80-95 ° C., and some of the acid will evaporate. This leads to evaporation of some of the acid, the vapours of which can be dangerous on inhalation. Loss of acid through evaporation will not only cause environmental problems, but also have an economic cost.
  • Previously some of the adverse effects have been relieved by adding a polymeric strong acid such as lignosulfonic acid or its salt (Patent WO 00/27220, PCT/NO99/00309).
  • In the present invention the above-mentioned problems associated with the use of acids have been reduced by adding a diol or triol, in particular glycerol. Surprisingly, it has been shown that the reduced corrosion rates goes far beyond that expected from a dilution of the acid.
  • By diol is meant any organic compound with at two hydroxyl group, e.g. ethylene glycol or propylene glycol. By triol is meant any organic compound with three hydroxyl groups, e.g. glycerol. Diols and triols can be produced by fermentation, by hydrolysis or by trans-esterification. Glycerol is produced in large quantities from the saponification of fats and the trans-esterification of fats to fatty acid methyl esters during biodiesel production.
  • The diol or triol is added in quantities from 10 to 90% of the final mixture with the acids, preferably from 40 to 60%.
  • Sugar and sugar alcohols have previously been described as corrosion inhibitors (FR is 2 391 261A). The advantages of simple diols and triols are several. They are cheaper. They are liquid at room temperature, and thus easier to use in any formulation. With the use of a diol like glycol or the triol glycerol we are not using scarce food resources as chemical raw materials.
  • Glycerol has been shown to reduce skin corrosion in a formic acid that has been partly neutralised with ammonia (NO 307 591 B). We here show that diols or triols also function as a corrosion inhibitor for metals without any neutralisation of the acids.
  • The following examples are meant to illustrate the invention without limiting its scope in any way.
  • EXAMPLES Corrosion Tests
  • Carbon steel coupons C1018 were used for the corrosion tests. The coupons were sonicated in acetone for 10 minutes, then dried in a heating cabinet, cooled in a desiccator and weighed. They were hung in polypropylene strips inside the test bottles filled with acid and the added corrosion inhibitor. The bottles were sealed with plastic film to prevent evaporation of the acid. The test bottles were placed on magnetic stirrers to prevent diffusion gradients within the solution. After 3 days the steel coupons were removed form the bottles and washed with warm water and acetone before they were dried in a heating cabinet, cooled in a desiccator and weighed. All experiments were done in duplicate and the average corrosion rates are given.
  • Corrosion rates, CR (mm/year), were determined from the weight loss of the steel coupons using this equation:
  • CR = Weight loss ( g ) * 365 d / year * 10 mm / cm ρ Steel ( g / cm 3 ) * Surface area ( cm 2 ) * d
      • ρSteel =7,718 g/cm3
      • Surface area =27, 2 cm2
  • The results from the different tests are shown in the tables below.
  • TABLE 1
    The effect of glycerol concentration for a strong organic acid.
    Corrosion Improve-
    Composition rate/mm/year ment/%
    10% water - 90% formic acid 6.7
    10% glycerol - 90% formic acid 4.1 38.8
    25% water - 75% formic acid 5.0
    25% glycerol - 75% formic acid 3.2 36.0
    50% water - 50% formic acid 7.5
    50% lignosulfonate solution - 50% formic acid 2.8 62.7
    50% glycerol - 50% formic acid 1.3 82.7
  • We see that at all concentrations glycerol is at least as effective as the commercially used lignosulfonates.
  • TABLE 2
    The effect of glycerol concentration for a weak organic acid.
    Corrosion Improve-
    Composition rate/mm/year ment/%
    10% water - 90% propionic acid 4.52
    10% glycerol - 90% propionic acid 0.70 84.5
    25% water - 75% propionic acid 5.57
    25% lignosulfonate solution - 75% 0.55 90.1
    propionic acid
    25% glycerol - 75% propionic acid 0.06 99.0
    50% water - 50% propionic acid 2.80
    50% lignosulfonate solution - 50% 1.15 58.9
    propionic acid
    50% glycerol - 50% propionic acid 0.031 98.9
  • We see that at all concentrations glycerol is at least as effective as the commerically used lignosulfonates.
  • TABLE 3
    The effect for various acids in a 50:50 wt % mixing ratio.
    Corrosion Improve-
    Composition rate/mm/year ment/%
    50% water - 50% concentrated 114.8
    hydrochloric acid
    50% glycerol - 50% concentrated 83.8 27.0
    hydrochloric acid
    50% water - 50% sulfuric acid (30%) 181
    50% glycerol - 50% sulfuric acid (30%) 25.9 85.7
    50% water - 50% propionic acid 2.8
    50% glycerol - 50% propionic acid 1.2 58.9
    50% water - 50% formic acid 7.5
    50% glycerol - 50% formic acid 1.3 82.7
  • We see that glycerol is effective for several mineral acids and organic acids.
  • TABLE 4
    The effect of various alcohols.
    Corrosion Improve-
    Composition rate/mm/year ment/%
    50% water - 50% formic acid 7.5
    50% glycerol - 50% formic acid 1.3 82.7
    50% glycol - 50% formic acid 2.9 61.7
    50% ethanol - 50% formic acid 9.8 −31.1
  • We see that the diol and triol shows good corrosion inhibition, while the simple alcohol does not.
  • Evaporation Tests
  • 500 ml of 50:50 wt % glycerol:formic acid, lignosulfonate:formic acid, water:formic acid solutions were made. Pure formic acid was included as a reference. Exactly 100 g of each solution was placed in 2 different beakers.
  • The samples were kept at room temperature with and without stirring. The weight was recorded at 4 hours, 26 hours, 58 hours and 89 hours. The results are presented in FIGS. 1 and 2. We see that all additives reduce the weight loss at room temperature, but the triol is much more effective than the other additives.

Claims (9)

1. A method of inhibiting corrosion of a metal that is in contact with an organic or inorganic acid comprising mixing with said organic or inorganic acid an amount of a diol or a triol sufficient to inhibit corrosion of said metal.
2. The method according to claim 1, wherein the diol or triol comprises 10-90% of the total mixture.
3. The method according to claim 1, a triol is mixed with said organic or inorganic acid and said triol is glycerol.
4. The method according to claim 1 further comprising mixing an additional corrosion inhibitor.
5. The method according to claim 1, wherein a diol is mixed with said organic or inorganic acid and said diol is glycol.
6. A composition comprising sulfuric acid, sulfurous acid, hydrochloric acid, or formic acid and a diol.
7. The composition according to claim 6, wherein said diol is glycol.
8. A composition comprising sulfuric acid, sulfurous acid, hydrochloric acid, or formic acid and a triol.
9. The composition according to claim 8, wherein said triol is glycerol.
US12/677,467 2007-09-13 2008-09-15 Corrosion inhibitor Abandoned US20110006264A1 (en)

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NO20074660 2007-09-13
NO20074660 2007-09-13
PCT/NO2008/000329 WO2009035341A1 (en) 2007-09-13 2008-09-15 Corrosion inhibitor

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JP (1) JP2010539329A (en)
CN (1) CN101878326A (en)
AU (1) AU2008297654A1 (en)
BR (1) BRPI0816974A8 (en)
WO (1) WO2009035341A1 (en)

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US180795A (en) * 1876-08-08 Improvement in music-stands
US1533622A (en) * 1921-12-28 1925-04-14 Buhler John J Varn Rust-removing compound
US2603622A (en) * 1948-10-01 1952-07-15 Berger Heinrich Halogen containing resin stabilized with an acetylene alcohol
US3004925A (en) * 1959-03-18 1961-10-17 Air Reduction Corrosion inhibition
US3349043A (en) * 1966-01-19 1967-10-24 Manning Dev Corp Methods and compositions for controlling oxidation of metal surfaces
US3772208A (en) * 1971-08-31 1973-11-13 Air Prod & Chem Corrosion inhibitor containing the ethynylation reaction product of butyraldehyde with acetylene
US5983756A (en) * 1997-11-19 1999-11-16 Warner-Lambert Company Aperture razor system and method of manufacture
US20030103865A1 (en) * 2001-10-29 2003-06-05 Libutti Bruce L. Corrosion inhibiting composition
US20040038840A1 (en) * 2002-04-24 2004-02-26 Shihying Lee Oxalic acid as a semiaqueous cleaning product for copper and dielectrics

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Publication number Priority date Publication date Assignee Title
GB683638A (en) * 1949-05-26 1952-12-03 Ethicon Suture Lab Inc Improvements in pickling bath
IN166983B (en) * 1985-02-11 1990-08-18 Henkel Corp
US5893756A (en) * 1997-08-26 1999-04-13 Lsi Logic Corporation Use of ethylene glycol as a corrosion inhibitor during cleaning after metal chemical mechanical polishing
NO305301B1 (en) * 1997-09-11 1999-05-10 Norsk Hydro As Aqueous preservative
NO307591B1 (en) * 1998-08-14 2000-05-02 Norsk Hydro As Aqueous preservative
US20060180795A1 (en) * 2005-02-17 2006-08-17 Mccormick David R Stable acid inhibitor formulations with improved performance, lower toxicity and minimal environmental issues
JP2006348324A (en) * 2005-06-14 2006-12-28 Sugimura Kagaku Kogyo Kk Corrosion inhibitor composition, acid purification solution, and acid purification method for metal

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US180795A (en) * 1876-08-08 Improvement in music-stands
US1533622A (en) * 1921-12-28 1925-04-14 Buhler John J Varn Rust-removing compound
US2603622A (en) * 1948-10-01 1952-07-15 Berger Heinrich Halogen containing resin stabilized with an acetylene alcohol
US3004925A (en) * 1959-03-18 1961-10-17 Air Reduction Corrosion inhibition
US3349043A (en) * 1966-01-19 1967-10-24 Manning Dev Corp Methods and compositions for controlling oxidation of metal surfaces
US3772208A (en) * 1971-08-31 1973-11-13 Air Prod & Chem Corrosion inhibitor containing the ethynylation reaction product of butyraldehyde with acetylene
US5983756A (en) * 1997-11-19 1999-11-16 Warner-Lambert Company Aperture razor system and method of manufacture
US20030103865A1 (en) * 2001-10-29 2003-06-05 Libutti Bruce L. Corrosion inhibiting composition
US20040038840A1 (en) * 2002-04-24 2004-02-26 Shihying Lee Oxalic acid as a semiaqueous cleaning product for copper and dielectrics

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EP2205776A1 (en) 2010-07-14
CN101878326A (en) 2010-11-03
JP2010539329A (en) 2010-12-16
BRPI0816974A2 (en) 2015-03-24
WO2009035341A1 (en) 2009-03-19
EP2205776A4 (en) 2012-02-29
AU2008297654A1 (en) 2009-03-19
BRPI0816974A8 (en) 2016-01-19

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