GB985117A - Corrosion inhibitor - Google Patents
Corrosion inhibitorInfo
- Publication number
- GB985117A GB985117A GB30626/65A GB3062665A GB985117A GB 985117 A GB985117 A GB 985117A GB 30626/65 A GB30626/65 A GB 30626/65A GB 3062665 A GB3062665 A GB 3062665A GB 985117 A GB985117 A GB 985117A
- Authority
- GB
- United Kingdom
- Prior art keywords
- corrosion
- ferrous metals
- hydroxybenzoic acid
- alkylene
- denotes
- 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
Links
- 230000007797 corrosion Effects 0.000 title abstract 5
- 238000005260 corrosion Methods 0.000 title abstract 5
- 239000003112 inhibitor Substances 0.000 title abstract 4
- 239000002184 metal Substances 0.000 abstract 5
- 229910052751 metal Inorganic materials 0.000 abstract 5
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 abstract 5
- -1 ferrous metals Chemical class 0.000 abstract 4
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 abstract 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 3
- 239000005977 Ethylene Substances 0.000 abstract 3
- SKZKKFZAGNVIMN-UHFFFAOYSA-N Salicilamide Chemical class NC(=O)C1=CC=CC=C1O SKZKKFZAGNVIMN-UHFFFAOYSA-N 0.000 abstract 3
- 125000002947 alkylene group Chemical group 0.000 abstract 3
- 150000001408 amides Chemical class 0.000 abstract 3
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 abstract 3
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 abstract 3
- 229960004889 salicylic acid Drugs 0.000 abstract 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 abstract 1
- 238000007792 addition Methods 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 239000012267 brine Substances 0.000 abstract 1
- 238000004140 cleaning Methods 0.000 abstract 1
- 239000008199 coating composition Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000001816 cooling Methods 0.000 abstract 1
- 238000005553 drilling Methods 0.000 abstract 1
- 239000007789 gas Substances 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 238000010348 incorporation Methods 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 238000002347 injection Methods 0.000 abstract 1
- 239000007924 injection Substances 0.000 abstract 1
- 239000004922 lacquer Substances 0.000 abstract 1
- 239000003973 paint Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- 238000005406 washing Methods 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 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
- 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
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting 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
- C23F11/14—Nitrogen-containing compounds
- C23F11/145—Amides; N-substituted amides
-
- 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
- Y10S507/939—Corrosion inhibitor
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention relates to hydroxybenzoic acid amides of the formula <FORM:0985117/C2/1> in which "alkylene" denotes an ethylene or trimethylene group and X is 2-4. The compounds may be prepared by heating a hydroxybenzoic acid with an appropriate amine, preferably under conditions which permit the escape of water as an azeotropic distillate. A typical example describes the preparation of an amide from salicylic acid and tetraethylene pentamine. The products are useful as corrosion inhibitors for ferrous metals (see Divisions C4, C5 and C7).ALSO:As corrosion inhibitors for ferrous metals, suitable for incorporation into paints, coating compositions or lacquers containing alkanolamines, and as corrosion-inhibiting additions to aqueous alkanolamine solutions for washing refinery gases in apparatus constructed of ferrous metal, use is made of hydroxybenzoic acid amides of the formula <FORM:0985117/C4-C5/1> in which "alkylene" denotes an ethylene or trimethylene group and X is 2-4 (see Division C2). A typical product is an amide prepared from salicyclic acid and tetraethylene pentamine.ALSO:As corrosion-inhibitors for ferrous metals, particularly for ferrous metals which come into contact with alkanolamines, use is made of hydroxybenzoic acid amides of the formula: <FORM:0985117/C6-C7/1> in which "alkylene" denotes an ethylene or trimethylene group and X is 2-4 (see Division C2). A typical product is an amide prepared from salicylic acid and tetraethylene pentamine. The products may also be used to inhibit corrosion in cooling towers, air-drilling and aerated mud systems, brine injection for flooding and/or disposal purposes, ballast systems on sea-going vessels, and pipeline cleaning or weighting.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14432161A | 1961-10-11 | 1961-10-11 | |
US218815A US3272861A (en) | 1961-10-11 | 1962-08-23 | Polyalkylene polyamine derivatives of hydroxybenzoic acid |
Publications (1)
Publication Number | Publication Date |
---|---|
GB985117A true GB985117A (en) | 1965-03-03 |
Family
ID=26841900
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB30626/65A Expired GB985117A (en) | 1961-10-11 | 1962-09-26 | Corrosion inhibitor |
Country Status (2)
Country | Link |
---|---|
US (1) | US3272861A (en) |
GB (1) | GB985117A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2222402A (en) * | 1988-08-30 | 1990-03-07 | Nat Res Dev | Biocidal polyamine-amides |
GB2222590A (en) * | 1988-08-30 | 1990-03-14 | Nat Reasearch Dev Corp | Therapeutic polyamine- amides |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3866603A (en) * | 1973-12-21 | 1975-02-18 | Shell Oil Co | Method of quench hardening with oil comprising mono (polyisobutenyl) succinimide |
US3925113A (en) * | 1973-12-21 | 1975-12-09 | Shell Oil Co | Quenching oil composition |
US4093557A (en) * | 1976-09-16 | 1978-06-06 | Hercules Incorporated | Process for inhibiting corrosion of metals in aqueous systems |
US4701224A (en) * | 1986-04-21 | 1987-10-20 | American Telephone And Telegraph Company, At&T Bell Laboratories | Water soluble condensation soldering flux |
US4990511A (en) * | 1988-08-03 | 1991-02-05 | Takeda Chemical Industries, Ltd. | Amide compounds, their production and use |
WO2011141341A1 (en) * | 2010-05-14 | 2011-11-17 | Iberhospitex, S.A. | Compounds for the synthesis of biostable polyurethane, polyurea or polyurea urethane polymers |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2400394A (en) * | 1944-12-14 | 1946-05-14 | Petrolite Corp | Process for breaking petroleum emulsions |
US2484146A (en) * | 1945-04-07 | 1949-10-11 | Houghton & Co E F | Lubricating composition |
US2636900A (en) * | 1949-06-20 | 1953-04-28 | Aschaffenburger Zellstoffwerke | Process for the purification of ortho-hydroxybenzamide |
US2695884A (en) * | 1952-04-10 | 1954-11-30 | Petrolite Corp | Process for breaking petroleum emulsions |
US2854323A (en) * | 1955-11-09 | 1958-09-30 | Petrolite Corp | Fuel oil composition |
US2935474A (en) * | 1955-11-28 | 1960-05-03 | Visco Products Co | Process of inhibiting corrosion and corrosion inhibiting compositions |
GB874206A (en) * | 1956-09-05 | 1961-08-02 | Knoll Ag | Basic derivatives of salicylamide |
US2993007A (en) * | 1957-03-08 | 1961-07-18 | Gen Mills Inc | Nu-alkylheterocyclic nitroge-containing derivatives as corrosion-inhibitors |
GB862721A (en) * | 1958-06-23 | 1961-03-15 | Miles Lab | Dialkylaminoethyl derivatives of salicylamides |
US3019196A (en) * | 1958-10-06 | 1962-01-30 | Gen Mills Inc | Process for inhibiting corrosion |
US3036128A (en) * | 1961-07-31 | 1962-05-22 | Upjohn Co | N-alkenyl-trialkoxybenzamides |
-
1962
- 1962-08-23 US US218815A patent/US3272861A/en not_active Expired - Lifetime
- 1962-09-26 GB GB30626/65A patent/GB985117A/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2222402A (en) * | 1988-08-30 | 1990-03-07 | Nat Res Dev | Biocidal polyamine-amides |
GB2222590A (en) * | 1988-08-30 | 1990-03-14 | Nat Reasearch Dev Corp | Therapeutic polyamine- amides |
GB2222402B (en) * | 1988-08-30 | 1992-01-22 | Nat Res Dev | Biocidal polyamine-amides |
GB2222590B (en) * | 1988-08-30 | 1992-07-22 | Nat Reasearch Dev Corp | Therapeutic polyamine-amides |
US5218000A (en) * | 1988-08-30 | 1993-06-08 | National Research Development Corporation | Therapeutic polyamine-amides |
Also Published As
Publication number | Publication date |
---|---|
US3272861A (en) | 1966-09-13 |
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