US3630932A - Corrosion-inhibited mineral acids - Google Patents
Corrosion-inhibited mineral acids Download PDFInfo
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- US3630932A US3630932A US789019A US3630932DA US3630932A US 3630932 A US3630932 A US 3630932A US 789019 A US789019 A US 789019A US 3630932D A US3630932D A US 3630932DA US 3630932 A US3630932 A US 3630932A
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- United States
- Prior art keywords
- corrosion
- acid
- inhibiting
- tetradecyn
- octyn
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- 238000005260 corrosion Methods 0.000 title abstract description 44
- 230000007797 corrosion Effects 0.000 title abstract description 44
- 239000002253 acid Substances 0.000 title description 28
- 229910052500 inorganic mineral Inorganic materials 0.000 title description 13
- 239000011707 mineral Substances 0.000 title description 13
- 150000007513 acids Chemical class 0.000 title description 2
- 229910052751 metal Inorganic materials 0.000 abstract description 24
- 239000002184 metal Substances 0.000 abstract description 24
- -1 FERROUS METALS Chemical class 0.000 abstract description 16
- CUUQUEAUUPYEKK-UHFFFAOYSA-N 4-ethyloct-1-yn-3-ol Chemical compound CCCCC(CC)C(O)C#C CUUQUEAUUPYEKK-UHFFFAOYSA-N 0.000 abstract description 9
- 150000002739 metals Chemical class 0.000 abstract description 9
- 239000011260 aqueous acid Substances 0.000 abstract description 4
- 238000010348 incorporation Methods 0.000 abstract description 2
- 230000002401 inhibitory effect Effects 0.000 description 26
- 239000003112 inhibitor Substances 0.000 description 24
- 235000010755 mineral Nutrition 0.000 description 12
- 239000000203 mixture Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- 230000005764 inhibitory process Effects 0.000 description 10
- 239000003929 acidic solution Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000003129 oil well Substances 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000005554 pickling Methods 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 2
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- JUWXVJKQNKKRLD-UHFFFAOYSA-N dec-3-yne Chemical compound CCCCCCC#CCC JUWXVJKQNKKRLD-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- 241000687607 Natalis Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- DQSGVVGOPRWTKI-QVFAWCHISA-N atazanavir sulfate Chemical compound [H+].[H+].[O-]S([O-])(=O)=O.C([C@H](NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1N=CC=CC=1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C1=CC=CC=C1 DQSGVVGOPRWTKI-QVFAWCHISA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229940000425 combination drug Drugs 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 238000012956 testing procedure Methods 0.000 description 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/164—Organic compounds containing a carbon-carbon triple bond
-
- 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
- C23G1/068—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors organic inhibitors compounds containing a C=C bond
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S507/00—Earth boring, well treating, and oil field chemistry
- Y10S507/933—Acidizing or formation destroying
- Y10S507/934—Acidizing or formation destroying with inhibitor
Definitions
- Aqueous acid solutions are inhibited against corrosion of metals, especially ferrous metals, by incorporation of a corrosion-inhibiting system composed of a combination of 4-ethyl-1-octyn-3-ol and 1,10-diethyl-7-tetradecyn-6,9- diol.
- This invention relates to the inhibition of metal corrosion in acidic solutions and is more particularly concerned with inhibited aqueous acid solutions suitable for the treatment of metals.
- Metal cleaning baths and pickling baths generally comprise aqueous solutions of inorganic acids such as sulfuric acid, hydrochloric acid, and phosphoric acid, and are useful in the cleaning and treatment of iron, zinc, ferrous alloys, and the like.
- inorganic acids such as sulfuric acid, hydrochloric acid, and phosphoric acid
- aqueous acidic baths In the use of aqueous acidic baths to treat metals, additives or inhibitors in the baths are desirable to prevent or inhibit corrosion or erosion of the metal surfaces. Similarly, in the field of oil-well acidizing, it is necessary to use inhibitors in order to prevent corrosion of the oilwell equipment by the aqueous acid solutions employed. Various other industrial operations also involve contact between an aqueous acidic solution and a metal, and an inhibitor must be used in order to minimize corrosion and/or consumption of the metal by such contact.
- a corrosion-inhibiting system comprising a plurality of components wherein relatively inexpensive compounds of poor corrosion-inhibiting action can be catalyzed or potentiated by the other component or components of the system so that the combination has a high corrosion-inhibiting activity even at elevated temperatures.
- It is a further object of this invention to provide a novel corrosion-inhibiting system comprising a combination of agents wherein one agent has a strong potentiating or catalyzing action upon the other agent so that the corrosion-inhibiting effectiveness of the combination is greater than the additive action of the components of the combination,
- a corrosion-inhibiting system comprising a combination of 4-ethyl-1-octyn-3-ol and 1,10-diethyl-7 tetradecyn-6,9-diol.
- the ratio between these two components of the corrosion-inhibiting system may vary, but the best results are obtained with weight ratios ranging between 1:10 and 10:1, preferably between 1:5 and 5:1 and most suitably between 1:2 and 2: 1.
- the acetylenic alcohol-acetylenic glycol inhibitor system of this invention is useful, in general, in the inhibition of corrosion of metal surfaces in contact with aqueous mineral acid solutions, such as hydrochloric acid, ulfuric acid, and phosphoric acid, for example in the acidizing of oil Wells, in electrolytic cleaning baths, and electrolytic refining of metals, as well as in metal cleaning and pickling baths.
- aqueous mineral acid solutions such as hydrochloric acid, ulfuric acid, and phosphoric acid
- the use of the above-described ethyl octynoldiethyl tetradecynol inhibitor system of this invention for corrosion inhibition of metals in aqueous mineral acid solutions is advantageous in that this corrosion inhibitor system can be employed in such acid solutions over a wide and useful concentration range.
- a further advantage of this inhibitor system is that it may be used at elevated temperatures to provide satisfactory corrosion inhibition, even when in relatively low concentration.
- the most effective amount of the corrosion-inhibiting system to be used in accordance with this invention can vary, depending upon local operation conditions.
- the temperature and other characteristics of the acid corrosive system may have a bearing upon the amount of inhibitor to be used.
- a concentration of the corrosion-inhibiting system of the invention between 0.01 and 2%, preferably between 0.01% to 1.2%, by weight of the aqueous acidic solution is an effective corrosion-inhibiting concentration, although higher concentrations can be used when conditions make them desirable, with a concentration between 0.05% to 0.75% by weight being of most general use, at elevated temperatures, e.g.
- the acidic solution can be dilute or concentrated and can be of any of the concentrations used in treating metals, e.g. ferrous metals, or for operations involving contact of acidic solutions with such metals, e.g. oil-well acidizing,
- the method used to determine the inhibiting properties of the system of the invention employs test specimens or coupons. To prepare the coupons, they are wiped with acetone to remove any residual oils or grease, and pickled for one minute in 10% hydrochloric acid to eliminate any scale and surface film. After pickling, the coupons are dipped in sodium bicarbonate solution, rinsed well in tap water, rinsed in distilled water, and finally dried with acetone. The clean and dry specimens are then weighed to the nearest 0.1 mg. In carrying out the evaluation, hydrochloroic acid of by weight concentration is used in order to duplicate oil-well acidizing conditions. The inhibitor system is added to 4 oz. test bottles, 100 ml.
- Inhibitor Percent inhibition 16 hrs. 4 ethyl 1 octyn 3 01 plus 1,10 diethyl- 7 tetradecyn 6,9 diol 99+ None These tests show the positive action of the combination of 4 ethyl 1 octyn 3 01 and 1.10 diethyl-7- tetradecyn 6,9 diol in accordance with this invention in inhibiting metal corrosion in an acid solution of high concentration at an elevated temperature only slightly below the boiling point of water, over a prolonged period of time, the components of the system being relatively inexpensive chemicals in the corrosion-inhibiting field.
- the inhibitor system of this invention can be prepared from individual quantities of 4-ethyl-l-octyn-3-ol and 1,10 diethyl 7 tetradecyn 6,9 diol
- a particularly advantageous source of these two chemicals is the reaction mixture obtained by the ethynylation of butyraldehyde with acetylene, using the well-known reaction wherein Z-ethylhexaldehyde and acetylene are reacted in the presence of a catalyst in an inert solvent medium, most commonly an ether, the reaction being carried out at various temperatures but which generally lie in the range of 0 to 50 C.
- the thus-produced mixture of 4 ethyl l octyn 3 01 and 1,10 diethyl 7 tetradecyn 6,9 diol will vary in composition somewhat, depending upon the specific reaction conditions, but the ratio of 4-ethyl 1 octyn-3-ol to LID-diethyl 7 tetradecyn 6,9 diol usually lies within the range of 5:1 to 1:4, and most commonly is about 1:1 to 2:1.
- the inert reaction medium is readily separated by distillation, but minor amounts of the solvent, e.g. up to 10% by weight or more, may be present and such presence does not interfere with the activity of the acetylenic hydroxy compounds.
- the mixture may also contain minor amounts of by-products produced by condensation, aldolization, or other reactions and are also unobjectionable. Such .byproducts may range up to 10% by weight but are usually less than about 5% by weight.
- reaction mixture of the character indicated is particularly attractive from a commercial standpoint since purification of the product of the ethynylation reaction is not required, yet the important benefits of the combination of 4-ethyl-1-octyn-3- 01 with 1,10-diethyl-7-tetradecyn-6,9-diol in the system of this invention are realized in the critical area of corrosion inhibition, i.e. high acid concentrations and high temperatures.
- the results shown in the foregoing test data are obtained when such a reaction mixture is employed in providing the corrosion-inhibiting system of this invention.
- the coupons used in the foregoing experiments were cut from a i in. sheet of a mild steel having the following typical analysis: 0.15% max. carbon, 0.300.60% manganese, 0.04% phosphorous, 0.05% sulfur, the balance iron.
- a corrosion-inhibited mineral acid comprising an aqueous solution of the mineral acid and a small, effective amount of a corrosion inhibiting mixture consisting essentially of 4-ethyl-1-octyn-3-ol and 1,10-diethyl-7- tetradecyn-6,9-diol wherein 4-cthyl-1-octyn-3-ol and 1,10- diethyl-7-tetradecyn'69-tliol are present in the relative weight ratios of 1:10 to 10:1.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Abstract
AQUEOUS ACID SOLUTIONS ARE INHIBITED AGAINST CORROSION OF METALS, ESPECIALLY FERROUS METALS, BY INCORPORATION OF A CORROSION-INHIBITING SYSTEM COMPOSED OF A COMBINATION OF 4-ETHYL-1-OCTYN-3-OL AND 1,10-DIETHYL-7-TETRADECYN-6,9DIOL.
Description
United States Patent 3,630,932 CORROSION-INHIBITED MINERAL ACIDS Robert J. Tedeschi, Whitehouse Station, and Paul W.
Natali, Middletown, N.J., assignors to Air Products and Chemicals, Inc., Allentown, Pa. No Drawing. Filed Dec. 31, 1968, Ser. No. 789,019 Int. Cl. Clld 7/26; C23g N06 US. Cl. 252-146 9 Claims ABSTRACT OF THE DISCLOSURE Aqueous acid solutions are inhibited against corrosion of metals, especially ferrous metals, by incorporation of a corrosion-inhibiting system composed of a combination of 4-ethyl-1-octyn-3-ol and 1,10-diethyl-7-tetradecyn-6,9- diol.
This invention relates to the inhibition of metal corrosion in acidic solutions and is more particularly concerned with inhibited aqueous acid solutions suitable for the treatment of metals.
Metal cleaning baths and pickling baths generally comprise aqueous solutions of inorganic acids such as sulfuric acid, hydrochloric acid, and phosphoric acid, and are useful in the cleaning and treatment of iron, zinc, ferrous alloys, and the like.
In the use of aqueous acidic baths to treat metals, additives or inhibitors in the baths are desirable to prevent or inhibit corrosion or erosion of the metal surfaces. Similarly, in the field of oil-well acidizing, it is necessary to use inhibitors in order to prevent corrosion of the oilwell equipment by the aqueous acid solutions employed. Various other industrial operations also involve contact between an aqueous acidic solution and a metal, and an inhibitor must be used in order to minimize corrosion and/or consumption of the metal by such contact.
If no corrosion inhibitor is present when the aqueous acidic solution comes into contact with the metal, excessive metal loss, production of undesirable metal surface properties, excessive consumption or loss of acid, and like adverse results will be experienced. Many different types of inhibitors have been proposed, but there has been a continuing search for corrosion inhibitors which can be used effectively in small concentrations, and which are economical to produce, since the use of inhibitors is a necessary expense and it is economically prudent to keep this expense at a minimum while, at the same time, realizing the desired inhibition of metallic corrosion or consumption. The need is also for corrosion inhibitors which are effective at high temperatures, e.g. 200 F. and above. such as are encountered in various operations involving acidic solutions, particularly oil-well acidizing where higher and higher temperatures are encountered as the well extends further into the earth.
While various corrosion-inhibiting agents have been proposed, all of such agents are not of equal effectiveness and of the many hundreds of agents which have been contemplated, only a few are sufficiently active to be commercially attractive. This is particularly true in the case of high-temperature operations. Some inhibitors which have been proposed are reasonably effective at low and moderate temperatures, but fail completely when high temperatures are encountered.
There has, therefore, been a continuing search for more effective inhibitors, or for ways of making a given inhibitor more effective. This search has involved the discovery of combinations of inhibitors which act together to provide an inhibitor system. However, many of these systems involve relatively expensive components so that, while they may be relatively effective in their corrosioninhibiting activity, there are disadvantages from an "ice economic standpoint, particularly if they have to be used in substantial quantities in order to bring about the desired corrosion-inhibiting activity. Similarly, many of these systems are ineffective at elevated temperatures. In particular, there is a need for a corrosion-inhibiting system comprising a plurality of components wherein relatively inexpensive compounds of poor corrosion-inhibiting action can be catalyzed or potentiated by the other component or components of the system so that the combination has a high corrosion-inhibiting activity even at elevated temperatures.
It is accordingly an object of this invention to provide a novel corrosion-inhibiting system involving a com bination of agents which is highly effective from the standpoint of corrosion-inhibiting activity and which is, at the same time, commercially attractive.
It is a further object of this invention to provide a novel corrosion-inhibiting system comprising a combination of agents wherein one agent has a strong potentiating or catalyzing action upon the other agent so that the corrosion-inhibiting effectiveness of the combination is greater than the additive action of the components of the combination,
It is another object of the invention to provide a corrosion-inhibiting system of the character indicated which is effective at high temperatures.
In accordance with this invention, it has been discovered that the above and other objects can be achieved by the provision of a corrosion-inhibiting system comprising a combination of 4-ethyl-1-octyn-3-ol and 1,10-diethyl-7 tetradecyn-6,9-diol. The ratio between these two components of the corrosion-inhibiting system may vary, but the best results are obtained with weight ratios ranging between 1:10 and 10:1, preferably between 1:5 and 5:1 and most suitably between 1:2 and 2: 1.
The acetylenic alcohol-acetylenic glycol inhibitor system of this invention is useful, in general, in the inhibition of corrosion of metal surfaces in contact with aqueous mineral acid solutions, such as hydrochloric acid, ulfuric acid, and phosphoric acid, for example in the acidizing of oil Wells, in electrolytic cleaning baths, and electrolytic refining of metals, as well as in metal cleaning and pickling baths. The use of the above-described ethyl octynoldiethyl tetradecynol inhibitor system of this invention for corrosion inhibition of metals in aqueous mineral acid solutions is advantageous in that this corrosion inhibitor system can be employed in such acid solutions over a wide and useful concentration range. A further advantage of this inhibitor system is that it may be used at elevated temperatures to provide satisfactory corrosion inhibition, even when in relatively low concentration.
The most effective amount of the corrosion-inhibiting system to be used in accordance with this invention can vary, depending upon local operation conditions. Thus, the temperature and other characteristics of the acid corrosive system may have a bearing upon the amount of inhibitor to be used. The higher the temperature and/ or the higher the acid concentration, the greater is the amount of corrosion inhibitor required to give optimum results. In general, however, it has been found that a concentration of the corrosion-inhibiting system of the invention between 0.01 and 2%, preferably between 0.01% to 1.2%, by weight of the aqueous acidic solution is an effective corrosion-inhibiting concentration, although higher concentrations can be used when conditions make them desirable, with a concentration between 0.05% to 0.75% by weight being of most general use, at elevated temperatures, e.g. in the neighborhood of 200 F. The acidic solution can be dilute or concentrated and can be of any of the concentrations used in treating metals, e.g. ferrous metals, or for operations involving contact of acidic solutions with such metals, e.g. oil-well acidizing,
3 and the like, for example to 80%. In most operations of the character indicated, acid concentrations of -15% by weight are employed, and nonoxidizing inorganic acids are used. However it is not intended to limit the invention to any specific use of acidic solutions or with respect to any specific metal or acid.
The method used to determine the inhibiting properties of the system of the invention employs test specimens or coupons. To prepare the coupons, they are wiped with acetone to remove any residual oils or grease, and pickled for one minute in 10% hydrochloric acid to eliminate any scale and surface film. After pickling, the coupons are dipped in sodium bicarbonate solution, rinsed well in tap water, rinsed in distilled water, and finally dried with acetone. The clean and dry specimens are then weighed to the nearest 0.1 mg. In carrying out the evaluation, hydrochloroic acid of by weight concentration is used in order to duplicate oil-well acidizing conditions. The inhibitor system is added to 4 oz. test bottles, 100 ml.
of the acid then added to each bottle; and the mixture shaken vigorously. The bottles are suspended in a constant-temperature bath consisting of a bell jar filled with ethylene glycol and equipped with a stirrer. The temperature is regulated to maintain the samples at 200:L-2 F. The bottles are placed in the bath /2 hour Percent inhibition \Vt loss of blank-wt. loss of test coupon wt. loss of blank When the acid concentration and temperature are such that the blank would be completely consumed by the acid in the absence of an inhibitor, the foregoing formula can he expressed as:
Percent inhibition original wt. test coupon\\'t. loss of test coupon original wt. test coupon EXAMPLE Using the testing procedure described above, and employing test coupons of mild steel 1 in. x 2 in. x in. in size, a mixture comprising 3 parts by weight of 4- ethyl-1-octyn-3-ol and 1 part by weight of 1,10-diethyl- 7-tetradecyn-6,9-diol was added to 15% hydrochloric acid, the mixture being added in the amount of 0.5% by weight of the acid, and the mixture evaluated for corrosion-inhibiting activity. At the same time a blank test, using the same acid but without any inhibitor, was made. Using the data obtained from these tests and applying the data in the formula set forth above for calculating percent inhibition, the following results were obtained:
Inhibitor: Percent inhibition 16 hrs. 4 ethyl 1 octyn 3 01 plus 1,10 diethyl- 7 tetradecyn 6,9 diol 99+ None These tests show the positive action of the combination of 4 ethyl 1 octyn 3 01 and 1.10 diethyl-7- tetradecyn 6,9 diol in accordance with this invention in inhibiting metal corrosion in an acid solution of high concentration at an elevated temperature only slightly below the boiling point of water, over a prolonged period of time, the components of the system being relatively inexpensive chemicals in the corrosion-inhibiting field.
While the inhibitor system of this invention can be prepared from individual quantities of 4-ethyl-l-octyn-3-ol and 1,10 diethyl 7 tetradecyn 6,9 diol, a particularly advantageous source of these two chemicals is the reaction mixture obtained by the ethynylation of butyraldehyde with acetylene, using the well-known reaction wherein Z-ethylhexaldehyde and acetylene are reacted in the presence of a catalyst in an inert solvent medium, most commonly an ether, the reaction being carried out at various temperatures but which generally lie in the range of 0 to 50 C. This reaction, which was originally proposed by Favorskii, and has been improved upon by several other workers, is well-described in the literature, and reference is made, for example, to the book Acetylenic Compounds by Thomas F. Rutledge (Reinhold Book Corp., 1968), especially pages 146 to 149, and to the footnotes referred to therein. In a typical operation the aldehyde and the acetylene are reacted in an acetal or an ether as the reaction medium at substantially atmospheric pressure at a temperature of 20'to 30 C., using solid KOH as catalyst in amounts which are substantially stoichiometric (usually slightly in excess) with respect to the aldehyde, the acetylene being in excess of the stoichiometric quantity. The thus-produced mixture of 4 ethyl l octyn 3 01 and 1,10 diethyl 7 tetradecyn 6,9 diol will vary in composition somewhat, depending upon the specific reaction conditions, but the ratio of 4-ethyl 1 octyn-3-ol to LID-diethyl 7 tetradecyn 6,9 diol usually lies within the range of 5:1 to 1:4, and most commonly is about 1:1 to 2:1. The inert reaction medium is readily separated by distillation, but minor amounts of the solvent, e.g. up to 10% by weight or more, may be present and such presence does not interfere with the activity of the acetylenic hydroxy compounds. The mixture may also contain minor amounts of by-products produced by condensation, aldolization, or other reactions and are also unobjectionable. Such .byproducts may range up to 10% by weight but are usually less than about 5% by weight.
It will be understood that a reaction mixture of the character indicated is particularly attractive from a commercial standpoint since purification of the product of the ethynylation reaction is not required, yet the important benefits of the combination of 4-ethyl-1-octyn-3- 01 with 1,10-diethyl-7-tetradecyn-6,9-diol in the system of this invention are realized in the critical area of corrosion inhibition, i.e. high acid concentrations and high temperatures. The results shown in the foregoing test data are obtained when such a reaction mixture is employed in providing the corrosion-inhibiting system of this invention.
The coupons used in the foregoing experiments were cut from a i in. sheet of a mild steel having the following typical analysis: 0.15% max. carbon, 0.300.60% manganese, 0.04% phosphorous, 0.05% sulfur, the balance iron.
It will be understood that various changes and modifications may be made in the operations described in the foregoing without departing from the scope of the invention as defined in the appended claims. It is intended, therefore, that all matter contained in the above descrip tion of the invention shall be interpreted as illustrative only and not as limitative.
We claim:
1. A corrosion-inhibited mineral acid comprising an aqueous solution of the mineral acid and a small, effective amount of a corrosion inhibiting mixture consisting essentially of 4-ethyl-1-octyn-3-ol and 1,10-diethyl-7- tetradecyn-6,9-diol wherein 4-cthyl-1-octyn-3-ol and 1,10- diethyl-7-tetradecyn'69-tliol are present in the relative weight ratios of 1:10 to 10:1.
2. A corrosion-inhibited acid as defined in claim 1 wherein the corrosion-inhibiting mixture is present in the amount of 0.01% to 2% by weight.
3. An inhibited mineral acid as defined in claim 4 wherein 4-ethy1-1-octyn-3-ol and 1,10-diethy1-7-tetradecyn-6,9-diol are present in the relative weight ratios of 1:4 to 5:1.
4. An inhibited mineral acid as defined in claim 2 wherein 4-ethyl-1-octyn-3-ol and 1,10-diethyl-7-tetradecyn-6,9-di0l are present in the relative weight ratio of 1:2 to 2: 1.
S. An inhibited mineral acid as defined in claim 2 wherein the mineral acid is hydrochloric acid.
6. A method of inhibiting corrosion of metals in a. mineral acid wherein the mineral acid contains a small, effective amount of a corrosion-inhibiting mixture con sisting essentially of 4-ethyl-1-octyn-3-ol and 1,10-diethy1- 7-tetradecyn-6,9-diol wherein 4-ethyl-1-0ctyn-3-ol and l,10-diethyl-7-tetradecyn-6,9-diol are present in the relative weight ratios of 1:10 to 10:1.
7. A method as defined in claim 6 wherein the corrosion-inhibiting mixture is present in the mineral acid in the amount of 0.01% to 2% by weight.
References Cited UNITED STATES PATENTS 3,125,475 3/1964 Livington et a1 134 41 X 10 3,231,507 1/1966 Beale, et a1 252-146 3,249,548 5/1966 Herman et al. 252 14s X 3,382,179 5/1968 Kenney et a1. 252-448 OTHER REFERENCES Rutledge, T. F., Acetylenic Compounds, Rheinhold Book Corp., 1968, pp. 146-9.
LEON D. ROSDOL, Primary Examiner 20 A. I. RADY, Assistant Examiner U.S. Cl. X.R.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US78901968A | 1968-12-31 | 1968-12-31 |
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| Publication Number | Publication Date |
|---|---|
| US3630932A true US3630932A (en) | 1971-12-28 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US789019A Expired - Lifetime US3630932A (en) | 1968-12-31 | 1968-12-31 | Corrosion-inhibited mineral acids |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5090013A (en) * | 1986-08-05 | 1992-02-18 | Ncr Corporation | Time slot protocol in the transmission of data in a data processing network |
| US5554320A (en) * | 1993-11-22 | 1996-09-10 | Yianakopoulos; Georges | Liquid cleaning compositions |
| US11034921B2 (en) | 2018-05-16 | 2021-06-15 | Adam Mason PRINCE | Method, kit, and composition for corrosion removal |
-
1968
- 1968-12-31 US US789019A patent/US3630932A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5090013A (en) * | 1986-08-05 | 1992-02-18 | Ncr Corporation | Time slot protocol in the transmission of data in a data processing network |
| US5554320A (en) * | 1993-11-22 | 1996-09-10 | Yianakopoulos; Georges | Liquid cleaning compositions |
| US11034921B2 (en) | 2018-05-16 | 2021-06-15 | Adam Mason PRINCE | Method, kit, and composition for corrosion removal |
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