WO2009035341A1 - Corrosion inhibitor - Google Patents

Corrosion inhibitor Download PDF

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Publication number
WO2009035341A1
WO2009035341A1 PCT/NO2008/000329 NO2008000329W WO2009035341A1 WO 2009035341 A1 WO2009035341 A1 WO 2009035341A1 NO 2008000329 W NO2008000329 W NO 2008000329W WO 2009035341 A1 WO2009035341 A1 WO 2009035341A1
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WO
WIPO (PCT)
Prior art keywords
acid
acids
triol
diol
corrosion
Prior art date
Application number
PCT/NO2008/000329
Other languages
French (fr)
Inventor
Bernt O. Myrvold
Kristin Sandersen Gretland
Tom Stylo
Rune Buvarp
Bente Seljebakken Klausen
Guro Elise Fredheim
Original Assignee
Borregaard Industries Limited Norge
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Borregaard Industries Limited Norge filed Critical Borregaard Industries Limited Norge
Priority to US12/677,467 priority Critical patent/US20110006264A1/en
Priority to CN200880112431XA priority patent/CN101878326A/en
Priority to EP08830690A priority patent/EP2205776A4/en
Priority to BRPI0816974A priority patent/BRPI0816974A8/en
Priority to JP2010524807A priority patent/JP2010539329A/en
Priority to AU2008297654A priority patent/AU2008297654A1/en
Publication of WO2009035341A1 publication Critical patent/WO2009035341A1/en

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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 offish, slaughterhouse waste, food waste and grass, and also in pig and chicken feed. Acetic acid is used for conservation offish. 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%.
  • Carbon steel coupons ClOl 8 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. AU experiments were done in duplicate and the average corrosion rates are given.
  • Table 1 The effect of glycerol concentration for a strong organic acid.
  • glycerol is at least as effective as the commercially used lignosulfonates.
  • glycerol is at least as effective as the commerically used lignosulfonates.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Hydrology & Water Resources (AREA)
  • Environmental & Geological Engineering (AREA)
  • Water Supply & Treatment (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

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

CORROSION INHIBITOR
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 offish, slaughterhouse waste, food waste and grass, and also in pig and chicken feed. Acetic acid is used for conservation offish. 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 0C, 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 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 ClOl 8 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. AU 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/vear * 10 mm/cm p Steel (g/cm3) * Surface area(cm2) * d /OStBeI = 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.
Figure imgf000004_0001
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.
Figure imgf000004_0002
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.
Figure imgf000004_0003
We see that glycerol is effective for several mineral acids and organic acids. Table 4. The effect of various alcohols.
Figure imgf000005_0001
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, waterformic 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 figure 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

1. The use of a diol or triol or a mixture of diols and/or triols as a corrosion inhibitor for organic or inorganic acids, or a mixture of acids.
2. The use according to claim 1 where the diol or triol or their mixture comprises 10- 90% of the total mixture.
3. The use according to claim 1 and 2 where the triol is glycerol and the diol is glycol.
4. The use according to claim 1 to 3 where the mixture contains further corrosion inhibitors.
PCT/NO2008/000329 2007-09-13 2008-09-15 Corrosion inhibitor WO2009035341A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
US12/677,467 US20110006264A1 (en) 2007-09-13 2008-09-15 Corrosion inhibitor
CN200880112431XA CN101878326A (en) 2007-09-13 2008-09-15 Inhibiter
EP08830690A EP2205776A4 (en) 2007-09-13 2008-09-15 Corrosion inhibitor
BRPI0816974A BRPI0816974A8 (en) 2007-09-13 2008-09-15 CORROSION INHIBITOR
JP2010524807A JP2010539329A (en) 2007-09-13 2008-09-15 Corrosion inhibitor
AU2008297654A AU2008297654A1 (en) 2007-09-13 2008-09-15 Corrosion inhibitor

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
NO20074660 2007-09-13
NO20074660 2007-09-13

Publications (1)

Publication Number Publication Date
WO2009035341A1 true WO2009035341A1 (en) 2009-03-19

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

Country Status (7)

Country Link
US (1) US20110006264A1 (en)
EP (1) EP2205776A4 (en)
JP (1) JP2010539329A (en)
CN (1) CN101878326A (en)
AU (1) AU2008297654A1 (en)
BR (1) BRPI0816974A8 (en)
WO (1) WO2009035341A1 (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
US3772208A (en) * 1971-08-31 1973-11-13 Air Prod & Chem Corrosion inhibitor containing the ethynylation reaction product of butyraldehyde with acetylene
EP0192130A2 (en) * 1985-02-11 1986-08-27 HENKEL CORPORATION (a Delaware corp.) Corrosion inhibitor composition
US20030103865A1 (en) * 2001-10-29 2003-06-05 Libutti Bruce L. Corrosion inhibiting composition
JP2006348324A (en) * 2005-06-14 2006-12-28 Sugimura Kagaku Kogyo Kk Corrosion inhibitor composition, acid purification solution, and acid purification method for metal

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US180795A (en) * 1876-08-08 Improvement in music-stands
US1533622A (en) * 1921-12-28 1925-04-14 Buhler John J Varn Rust-removing compound
GB683638A (en) * 1949-05-26 1952-12-03 Ethicon Suture Lab Inc Improvements in pickling bath
US3349043A (en) * 1966-01-19 1967-10-24 Manning Dev Corp Methods and compositions for controlling oxidation of metal surfaces
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
US5983756A (en) * 1997-11-19 1999-11-16 Warner-Lambert Company Aperture razor system and method of manufacture
NO307591B1 (en) * 1998-08-14 2000-05-02 Norsk Hydro As Aqueous preservative
AU2003225178A1 (en) * 2002-04-24 2003-11-10 Ekc Technology, Inc. Oxalic acid as a cleaning product for aluminium, copper and dielectric surfaces
US20060180795A1 (en) * 2005-02-17 2006-08-17 Mccormick David R Stable acid inhibitor formulations with improved performance, lower toxicity and minimal environmental issues

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
US3772208A (en) * 1971-08-31 1973-11-13 Air Prod & Chem Corrosion inhibitor containing the ethynylation reaction product of butyraldehyde with acetylene
EP0192130A2 (en) * 1985-02-11 1986-08-27 HENKEL CORPORATION (a Delaware corp.) Corrosion inhibitor composition
US20030103865A1 (en) * 2001-10-29 2003-06-05 Libutti Bruce L. Corrosion inhibiting composition
JP2006348324A (en) * 2005-06-14 2006-12-28 Sugimura Kagaku Kogyo Kk Corrosion inhibitor composition, acid purification solution, and acid purification method for metal

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP2205776A4 *

Also Published As

Publication number Publication date
BRPI0816974A8 (en) 2016-01-19
EP2205776A4 (en) 2012-02-29
JP2010539329A (en) 2010-12-16
US20110006264A1 (en) 2011-01-13
AU2008297654A1 (en) 2009-03-19
BRPI0816974A2 (en) 2015-03-24
CN101878326A (en) 2010-11-03
EP2205776A1 (en) 2010-07-14

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