US2617771A - Corrosion retarder - Google Patents
Corrosion retarder Download PDFInfo
- Publication number
- US2617771A US2617771A US41727A US4172748A US2617771A US 2617771 A US2617771 A US 2617771A US 41727 A US41727 A US 41727A US 4172748 A US4172748 A US 4172748A US 2617771 A US2617771 A US 2617771A
- Authority
- US
- United States
- Prior art keywords
- thio
- corrosion
- lauryl
- acid
- retarders
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 230000007797 corrosion Effects 0.000 title claims description 12
- 238000005260 corrosion Methods 0.000 title claims description 12
- 239000002253 acid Substances 0.000 claims description 15
- 239000002184 metal Substances 0.000 claims description 13
- 229910052751 metal Inorganic materials 0.000 claims description 13
- 150000002739 metals Chemical class 0.000 claims description 8
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims description 5
- QHTSJPCQUQAHSQ-UHFFFAOYSA-M 1-dodecylpyridin-1-ium thiocyanate Chemical compound [S-]C#N.C(CCCCCCCCCCC)[N+]1=CC=CC=C1 QHTSJPCQUQAHSQ-UHFFFAOYSA-M 0.000 claims description 4
- FYNVMNJSYWEFFH-UHFFFAOYSA-M benzyl-dodecyl-dimethylazanium;thiocyanate Chemical compound [S-]C#N.CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 FYNVMNJSYWEFFH-UHFFFAOYSA-M 0.000 claims description 3
- 239000011260 aqueous acid Substances 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- -1 aralkyl thio-cyanates Chemical class 0.000 description 10
- 238000005554 pickling Methods 0.000 description 7
- 150000007513 acids Chemical class 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- GKQHIYSTBXDYNQ-UHFFFAOYSA-M 1-dodecylpyridin-1-ium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+]1=CC=CC=C1 GKQHIYSTBXDYNQ-UHFFFAOYSA-M 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000010687 lubricating oil Substances 0.000 description 3
- 230000009972 noncorrosive effect Effects 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M thiocyanate group Chemical group [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 2
- 239000011149 active material Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- JBIROUFYLSSYDX-UHFFFAOYSA-M benzododecinium chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 JBIROUFYLSSYDX-UHFFFAOYSA-M 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- ABNDFSOIUFLJAH-UHFFFAOYSA-N benzyl thiocyanate Chemical compound N#CSCC1=CC=CC=C1 ABNDFSOIUFLJAH-UHFFFAOYSA-N 0.000 description 2
- 229930007927 cymene Natural products 0.000 description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003567 thiocyanates Chemical class 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- NDZFNTHGIIQMQI-UHFFFAOYSA-N 1-benzylpyridin-1-ium Chemical compound C=1C=CC=C[N+]=1CC1=CC=CC=C1 NDZFNTHGIIQMQI-UHFFFAOYSA-N 0.000 description 1
- INUMMPHTUPBOEU-UHFFFAOYSA-N 1-phenylacridine Chemical compound C1=CC=CC=C1C1=CC=CC2=NC3=CC=CC=C3C=C12 INUMMPHTUPBOEU-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000001996 bearing alloy Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 235000021384 green leafy vegetables Nutrition 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Chemical compound CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003129 oil well Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G1/00—Cleaning or pickling metallic material with solutions or molten salts
- C23G1/02—Cleaning or pickling metallic material with solutions or molten salts with acid solutions
- C23G1/04—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors
- C23G1/06—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors organic inhibitors
- C23G1/065—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors organic inhibitors sulfur-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-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
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/04—Inhibiting 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
Definitions
- My invention relates more particularly to retarders of corrosion of metals by acids.
- aralkyl thio-cyanates such as benzyl and cymene thio-cyanates. These are typical examples of aralkyl thio-cyanates, each having a methyl group, to which the thio-cyanate group is attached, and the cymene having, in addition, a propyl group.
- these compounds are of low solubility in acid pickling baths.
- benzyl thio-cyanate has not only an exceedingly disagreeable odor, but toxic and lachrymatory properties, the effects of which are aggravated by its low solubility and consequent tendency to collect at the surface of the bath and spatter into the atmosphere. For these reasons, these compounds have heretofore had little importance, except under conditions permitting of vigorous agitation.
- agents of the surface active category are the quaternary ammonium compounds, such as lauryl pyridinium chloride and lauryl dimethyl benzyl ammonium chloride. These are selected examples of quaternary ammonium compounds in which the nitrogen is in the ringand chain respectively. They are not only quite solubl in acid pickling baths, but also have the property of increasing the solubility of other organic compounds, including the thio-cyanates. When used in pickling baths, their saponaceous character causes them to form a foam layer upon the surface.
- Example I Metal, steel Acid, sulphuric, 15% Temperature, C. Corrosion retarder None Percent retarder by weight Weight loss per sq. c. in.
- Example II LPC LDBAC Metal, steel Acid, sulphuric, 15% Temperature, 75 C. Corrosion retarder None LDBATC ercent retarder by weight Weight loss per sq.
- lauryl dimethyl benzyl ammonium thio-cyanate and lauryl pyridinium thio-cyanate rank high among corrosion retarders, and when it is remembered that they, have the advantage over most of them of high water solubility, non-toxicity, and freedom from offensive odor, theirimportance as corrosion retarders will be manifest.
- Corrosion retarders are useful Wherever acids are handled in metal equipment, of which pickling of metal is only one of many illustrations, acid treatment of oil wells being another. Another use of such retarders is in lubricants, which are liable to develop acidity through oxidation, by contact with air. Organic acids developed in lubricating oils, such as those used in automotive crankcases, are mild compared with pickling acids, but the time factor is measured in months, instead of hours, and in the long run the corrosive effect of such acids may be very serious, especially upon bearing alloys such as those composed of lead, tin, copper and less common metals. It is difficult to give a quantitative measure of the effect of corrosion retarders in lubricating oils, as the matter is complicated by wear. Nevertheless,
- a composition substantially non-corrosive to metals comprising a dilute aqeous solution of an inorganic acid and 0.005 to 5 per cent by weight of a quaternary ammonium compound selected from the group consisting of lauryl pyridinium thiocyanate and lauryl dimethyl benzyl ammonium thiocyanate.
- a composition substantially non-corrosive to metals comprising a dilute aqueous solution of sulfuric acid and 0.005 to 5 per cent by weight of lauryl pyridinium thiocyanate.
- a composition substantially non-corrosive to metals comprising a dilute aqueous solution of sulfuric acid and 0.005 to 5' percent by weight of lauryl dimethyl benzyl amino'ni'num thiocyanate.
- the method of protecting metals against corrosion by dilute aqueous acids which comprises incorporating in the acid 0.005 to 5.0 per cent by weight of a quaternary ammonium compound selected from the group consisting of lauryl pyridinium thiocyanate and lauryl dimethyl benzyl ammonium thiocyanate.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
Description
Patented Nov. 11, 1952 UNITED STATES greens orrrcs? Hooker Electrochemical Company, Niagara Falls, N. Y., a corporation of New York No Drawing. Original application September 27,
1946, Serial No.
699,640, now Patent No.
2,459,119, dated January 11, 1949. Divided and this application July 30, 1948, Serial No. 41,727
4. Claims.
My invention relates more particularly to retarders of corrosion of metals by acids.
It is known that certain substances exert a protective eifect upon metals, against attack of acids thereon, by rendering the metal passive with respect to the acid, i. e., as anti-catalysts. I will refer to these hereinafter as inhibitors. It is also known that certain other substances exert a protective effect by interposing a film between the metal and the acid. These are of the nature of detergents, or dispersing or Wetting agents, characterized by low surface tension. I will refer to these hereinafter as surface active materials.
Among the agents of the inhibitor category are the aralkyl thio-cyanates, such as benzyl and cymene thio-cyanates. These are typical examples of aralkyl thio-cyanates, each having a methyl group, to which the thio-cyanate group is attached, and the cymene having, in addition, a propyl group. However, these compounds are of low solubility in acid pickling baths. Also, benzyl thio-cyanate has not only an exceedingly disagreeable odor, but toxic and lachrymatory properties, the effects of which are aggravated by its low solubility and consequent tendency to collect at the surface of the bath and spatter into the atmosphere. For these reasons, these compounds have heretofore had little importance, except under conditions permitting of vigorous agitation.
Among the agents of the surface active category are the quaternary ammonium compounds, such as lauryl pyridinium chloride and lauryl dimethyl benzyl ammonium chloride. These are selected examples of quaternary ammonium compounds in which the nitrogen is in the ringand chain respectively. They are not only quite solubl in acid pickling baths, but also have the property of increasing the solubility of other organic compounds, including the thio-cyanates. When used in pickling baths, their saponaceous character causes them to form a foam layer upon the surface.
Th eiiectiveness of these surface active materials is illustrated by the following examples, in which the abbreviations LPG and LDBAC stand for lauryl pyridinium chloride and lauryl dimethyl benzyl ammonium chloride respectively, and the expression protection per cent signifies the extent to which the agent is effective in eliminating corrosion altogether:
Example I Metal, steel Acid, sulphuric, 15% Temperature, C. Corrosion retarder None Percent retarder by weight Weight loss per sq. c. in.
per hour g .119 .048 .0076 Protection, percent 60.0 93.6
It will be seen from the above examples that the addition of minute quantities of these materials to acid pickling baths greatly diminishes the attack upon steel.
I have now found that the analogous quaternary ammonium thio-cyanates, i. e., lauryl pyridinium thio-cyanate and lauryl dimethyl benzyl ammonium thio-cyanate, are very soluble in acid pickling baths, for practical purposes odorless and non-toxic and very efiective as corrosion retarders.
This is illustrated by the following example, to which I have also added benzyl pyridinium thicyanate for comparison, and in which these compounds are denoted by the abbreviations LDBATC, LPTC and BPTC respectively:
Example II LPC LDBAC Metal, steel Acid, sulphuric, 15% Temperature, 75 C. Corrosion retarder None LDBATC ercent retarder by weight Weight loss per sq.
c. m. per hr. g .119 .0047 .0021 Protection, percent 96.0 98.2
It will be seen by comparison Examples I and II that these alkyl quaternary ammonium thiocyanates are much more effective as retarders of corros1on than the corresponding chlorides. It W111 also be seen that these alkyl quaternary am- LPTC BPTC
monium thio-cyanates are much superior to the Protection, Wt. Percent Percent Triethylamine 0. 15 10. Aniline 0. 09 14. 5 Pyridine 0. 08 19.0 Quinoline- 0. 13 49. 4 Acridine. 0. 18 82. 4 2-me-quinol1ne 0. 53. 0 me-acridine 0. 20 81.8 Phenyl acridine 0. 29 90. 2 Nitrogen bases 0.1 88. Lauryl pyridinium chloride 0. 1 85. Lauryl dimcthyl benzyl ammo um thio-cyanate 1 0. 02 96, Lauryl pyridinium thio-cyanate 0.02 98. 2 Lauryl pyridinium thio-cyanate 0.01 90. 4
t will be seen from the above that lauryl dimethyl benzyl ammonium thio-cyanate and lauryl pyridinium thio-cyanate rank high among corrosion retarders, and when it is remembered that they, have the advantage over most of them of high water solubility, non-toxicity, and freedom from offensive odor, theirimportance as corrosion retarders will be manifest.
Corrosion retarders are useful Wherever acids are handled in metal equipment, of which pickling of metal is only one of many illustrations, acid treatment of oil wells being another. Another use of such retarders is in lubricants, which are liable to develop acidity through oxidation, by contact with air. Organic acids developed in lubricating oils, such as those used in automotive crankcases, are mild compared with pickling acids, but the time factor is measured in months, instead of hours, and in the long run the corrosive effect of such acids may be very serious, especially upon bearing alloys such as those composed of lead, tin, copper and less common metals. It is difficult to give a quantitative measure of the effect of corrosion retarders in lubricating oils, as the matter is complicated by wear. Nevertheless,
visual comparison of the effects of lubricating oils upon bearings, with and without my retarders, indicates that my retarders have a useful effect in such oils.
While I have given examples of the results obtained with my compositions only in proportions ranging from 0.02 to 0.1 per cent by weight, I do not wish to be held to these limits, as my retarders are useful in proportions as low as .005 per cent, and there is no objection to using up to 5 per cent of the retarder.
This application is a division of my co-pending application, Serial Number 699,640 filed September 27, 1946, now Patent No. 2,459,119 issued January 11, 1949.
I claim as my invention:
1. A composition substantially non-corrosive to metals comprising a dilute aqeous solution of an inorganic acid and 0.005 to 5 per cent by weight of a quaternary ammonium compound selected from the group consisting of lauryl pyridinium thiocyanate and lauryl dimethyl benzyl ammonium thiocyanate.
2. A composition substantially non-corrosive to metals comprising a dilute aqueous solution of sulfuric acid and 0.005 to 5 per cent by weight of lauryl pyridinium thiocyanate.
3. A composition substantially non-corrosive to metals comprising a dilute aqueous solution of sulfuric acid and 0.005 to 5' percent by weight of lauryl dimethyl benzyl amino'ni'num thiocyanate.
4. The method of protecting metals against corrosion by dilute aqueous acids which comprises incorporating in the acid 0.005 to 5.0 per cent by weight of a quaternary ammonium compound selected from the group consisting of lauryl pyridinium thiocyanate and lauryl dimethyl benzyl ammonium thiocyanate.
JOHN T. RUCKER.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,006,216 MacArthur et a1. June 25, 1 935 2,203,649 Felkers June 4, 1940 2,254,940 Endres Sept. 2, 1941 2,321,517 Rosen June 8, 1943 2,340,996 Smyers Feb. 8, 1944 2,402,526 Pikl -1 June 18, 1946
Claims (1)
- 4. THE METHOD OF PROTECTING METALS AGAINST CORROSION BY DILUTE AQUEOUS ACIDS WHICH COMPRISES INCORPORATING IN THE ACID 0.005 TO 5.0 PER CENT BY WEIGHT OF A QUATERNARY AMMONIUM COMPOUND SELECTED FROM THE GROUP CONSISTING OF LAURYL PYRIDINIUM THIOCYANATE AND LAURYL DIMETHYL BENZYL AMMONIUM THIOCYANATE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41727A US2617771A (en) | 1946-09-27 | 1948-07-30 | Corrosion retarder |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US699640A US2459119A (en) | 1946-09-27 | 1946-09-27 | Corrosion retarder |
| US41727A US2617771A (en) | 1946-09-27 | 1948-07-30 | Corrosion retarder |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2617771A true US2617771A (en) | 1952-11-11 |
Family
ID=26718460
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US41727A Expired - Lifetime US2617771A (en) | 1946-09-27 | 1948-07-30 | Corrosion retarder |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2617771A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2959555A (en) * | 1956-09-28 | 1960-11-08 | Dow Chemical Co | Copper and iron containing scale removal from ferrous metal |
| US3047510A (en) * | 1957-06-05 | 1962-07-31 | Armour & Co | Corrosion inhibiting compositions and process |
| US3124534A (en) * | 1964-03-10 | Moocxch | ||
| US3133028A (en) * | 1960-02-18 | 1964-05-12 | Wright Chem Corp | Corrosion inhibition |
| EP0519594A1 (en) * | 1991-05-29 | 1992-12-23 | Petrolite Corporation | Corrosion inhibition in highly acidic environments by use of pyridine salts in combination with certain cationic surfactants |
| WO2017112721A1 (en) * | 2015-12-22 | 2017-06-29 | Albemarle Corporation | Corrosion inhibitors and related processes for their production and use |
| CN107973719A (en) * | 2016-10-24 | 2018-05-01 | 中国石油化工股份有限公司 | A kind of preparation method of inhibition component and products thereof and application |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2006216A (en) * | 1932-02-26 | 1935-06-25 | Ici Ltd | Inhibitor |
| US2203649A (en) * | 1937-07-28 | 1940-06-04 | Stikstofbindingsindustrie Nede | Acid solution |
| US2254940A (en) * | 1937-09-09 | 1941-09-02 | Endres Gunther | Rust prevention |
| US2321517A (en) * | 1941-01-02 | 1943-06-08 | Standard Oil Dev Co | Lubricant composition |
| US2340996A (en) * | 1944-02-08 | Coating composition | ||
| US2402526A (en) * | 1941-04-04 | 1946-06-18 | Du Pont | Thiocyanate quaternary compounds and method of preparing the same |
-
1948
- 1948-07-30 US US41727A patent/US2617771A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2340996A (en) * | 1944-02-08 | Coating composition | ||
| US2006216A (en) * | 1932-02-26 | 1935-06-25 | Ici Ltd | Inhibitor |
| US2203649A (en) * | 1937-07-28 | 1940-06-04 | Stikstofbindingsindustrie Nede | Acid solution |
| US2254940A (en) * | 1937-09-09 | 1941-09-02 | Endres Gunther | Rust prevention |
| US2321517A (en) * | 1941-01-02 | 1943-06-08 | Standard Oil Dev Co | Lubricant composition |
| US2402526A (en) * | 1941-04-04 | 1946-06-18 | Du Pont | Thiocyanate quaternary compounds and method of preparing the same |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3124534A (en) * | 1964-03-10 | Moocxch | ||
| US2959555A (en) * | 1956-09-28 | 1960-11-08 | Dow Chemical Co | Copper and iron containing scale removal from ferrous metal |
| US3047510A (en) * | 1957-06-05 | 1962-07-31 | Armour & Co | Corrosion inhibiting compositions and process |
| US3133028A (en) * | 1960-02-18 | 1964-05-12 | Wright Chem Corp | Corrosion inhibition |
| EP0519594A1 (en) * | 1991-05-29 | 1992-12-23 | Petrolite Corporation | Corrosion inhibition in highly acidic environments by use of pyridine salts in combination with certain cationic surfactants |
| US5336441A (en) * | 1991-05-29 | 1994-08-09 | Petrolite Corporation | Corrosion inhibition in highly acidic environments by use of pyridine salts in combination with certain cationic surfactants |
| WO2017112721A1 (en) * | 2015-12-22 | 2017-06-29 | Albemarle Corporation | Corrosion inhibitors and related processes for their production and use |
| CN107973719A (en) * | 2016-10-24 | 2018-05-01 | 中国石油化工股份有限公司 | A kind of preparation method of inhibition component and products thereof and application |
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