GB692413A - Improvements in or relating to methods of cleaning ferrous metal surfaces and to baths for use therein - Google Patents
Improvements in or relating to methods of cleaning ferrous metal surfaces and to baths for use thereinInfo
- Publication number
- GB692413A GB692413A GB17426/48A GB1742648A GB692413A GB 692413 A GB692413 A GB 692413A GB 17426/48 A GB17426/48 A GB 17426/48A GB 1742648 A GB1742648 A GB 1742648A GB 692413 A GB692413 A GB 692413A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- mercaptobenzothiazole
- compounds
- ethylene oxide
- integer
- 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
- 229910052751 metal Inorganic materials 0.000 title abstract 2
- 239000002184 metal Substances 0.000 title abstract 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 title 1
- 238000004140 cleaning Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 abstract 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 abstract 5
- 150000001875 compounds Chemical class 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 3
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 abstract 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- GBDZXPJXOMHESU-UHFFFAOYSA-N 1,2,3,4-tetrachlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1Cl GBDZXPJXOMHESU-UHFFFAOYSA-N 0.000 abstract 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- MRORKWHSOOKUDV-UHFFFAOYSA-N 1h-benzo[e][1,3]benzothiazole-2-thione Chemical compound C1=CC=C2C(NC(S3)=S)=C3C=CC2=C1 MRORKWHSOOKUDV-UHFFFAOYSA-N 0.000 abstract 1
- PRCSESBJUUBNDJ-UHFFFAOYSA-N 2-methyl-6-(1,3-thiazol-2-yl)benzenethiol Chemical compound SC1=C(C=CC=C1C=1SC=CN1)C PRCSESBJUUBNDJ-UHFFFAOYSA-N 0.000 abstract 1
- MYBFPRUVQGKNIV-UHFFFAOYSA-N 4-chloro-3h-1,3-benzothiazole-2-thione Chemical compound C1=CC=C2SC(S)=NC2=C1Cl MYBFPRUVQGKNIV-UHFFFAOYSA-N 0.000 abstract 1
- GUISIVZZEFLXQH-UHFFFAOYSA-N 4-phenyl-3h-1,3-benzothiazole-2-thione Chemical compound C1=CC=C2SC(=S)NC2=C1C1=CC=CC=C1 GUISIVZZEFLXQH-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 1
- -1 Ferrous metals Chemical class 0.000 abstract 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 abstract 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000000732 arylene group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- 235000011187 glycerol Nutrition 0.000 abstract 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 239000002198 insoluble material Substances 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 235000010755 mineral Nutrition 0.000 abstract 1
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 abstract 1
- 238000005554 pickling Methods 0.000 abstract 1
- 235000011118 potassium hydroxide Nutrition 0.000 abstract 1
- 238000002360 preparation method Methods 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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Compounds of the general formula <FORM:0692413/IV (b)/1> where Ar is an ortho arylene radical, R is an alkylene group and n is an integer, for use as pickling inhibitors, are prepared by introducing into 2-mercaptoarylenethiazoles one or more hydroxyalkyl radicals. The former may be 2-mercaptobenzothiazole, 2 - mercaptonaphthothiazole, 2 - mercapto - 4 - phenylbenzothiazole, 2 - mercaptochlorobenzothiazole or 2 - mercaptotolylthiazole and condensation may be effected with ethylene oxide, propylene oxide, glycide, epichlorhydrin, glycol, glycerine or polyglyamine or two such compounds may be caused to react consecutively. Alkaline reacting agents or nickel sulphate may be employed as catalysts. In an example, 2-mercaptobenzothiazole is dissolved in dioxane, absorptive carbon added and ethylene oxide passed into the solution at 96-105 DEG C.; insoluble material is, when reaction ceases, filtered from the hot solution, solvent removed and the residue heated to 90 DEG C. under 5 mm. pressure. The product is then recrystallized from benzene. Alternatively, monochlorobenzene, orthodichlorobenzene, tetrachlorobenzene or the diethyl ether of diethylene glycol may be used as solvent. The reaction of mercaptobenzothiazole with ethylene oxide in varying ratios in the presence of caustic potash is also described to yield products in which n varies from 1-15. Products may also be prepared as described in Specification 692,414.ALSO:Ferrous metals are pickled in a mineral acid solution containing a small proportion of a compound of the formula <FORM:0692413/II/1> where Ar is an ortho arylene group, R is an alkyline radical and n is an integer: R may be an ethylene group and n may be between 5 and 31. The preparation of these compounds is described, (see Group IV(b)), and Specification 692,414, [Group IV(b)], is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US758729A US2518109A (en) | 1947-07-02 | 1947-07-02 | Pickling of metals |
Publications (1)
Publication Number | Publication Date |
---|---|
GB692413A true GB692413A (en) | 1953-06-03 |
Family
ID=25052860
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB17426/48A Expired GB692413A (en) | 1947-07-02 | 1948-06-29 | Improvements in or relating to methods of cleaning ferrous metal surfaces and to baths for use therein |
Country Status (2)
Country | Link |
---|---|
US (1) | US2518109A (en) |
GB (1) | GB692413A (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1565349A (en) * | 1975-10-20 | 1980-04-16 | Albright & Wilson | Aluminium polishing compositions |
US4329475A (en) * | 1980-11-10 | 1982-05-11 | Olin Corporation | Selected poly(oxyalkylated) 1,3,4-thiadiazoles and their use as corrosion inhibitors |
US4306988A (en) * | 1980-11-10 | 1981-12-22 | Olin Corporation | Selected poly(oxyalkylated) 1,3,4-thiadiazoles and their use as corrosion inhibitors |
US4349458A (en) * | 1980-11-10 | 1982-09-14 | Olin Corporation | Selected poly(oxyalkylated) 1,3,4-thiadiazoles in acid baths and their use as corrosion inhibitors |
DE10123210C1 (en) * | 2001-05-12 | 2002-10-02 | Clariant Gmbh | New ether carboxylic acids and salts derived from alkoxylated mercaptobenzothiazoles are used as corrosion inhibitors in metal working and petroleum and natural gas recovery and processing |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1990963A (en) * | 1934-07-07 | 1935-02-12 | Wingfoot Corp | Pickling inhibitor |
US2383681A (en) * | 1942-09-11 | 1945-08-28 | Du Pont | Composition and process for cleaning and pickling ferrous metals |
-
1947
- 1947-07-02 US US758729A patent/US2518109A/en not_active Expired - Lifetime
-
1948
- 1948-06-29 GB GB17426/48A patent/GB692413A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
US2518109A (en) | 1950-08-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1005872A (en) | Process for the manufacture of sulphonated organosilicon products | |
GB930296A (en) | The preparation of acylamino compounds | |
GB692413A (en) | Improvements in or relating to methods of cleaning ferrous metal surfaces and to baths for use therein | |
GB1094205A (en) | Process for the preparation of amino-acid surface active agents | |
Mariella | Condensations of unsymmetrical ketones. I. condensations with ethyl formate | |
GB823191A (en) | New phenthiazine derivatives and processes for their preparation | |
US2642430A (en) | Hydroxy substituted aliphatic ether derivatives of nitrogen heterocyclics | |
US2382433A (en) | Is bej x | |
US2857392A (en) | Certificate of correction | |
GB1047061A (en) | Polymers and a process for the preparation thereof | |
GB754679A (en) | Improvements in or relating to polyoxyalkylated tert.-carbinamines | |
GB926898A (en) | New polyether carboxylic acids and process for their manufacture | |
US2025876A (en) | Preparation of aryl-amines | |
GB1123762A (en) | Improved process for the production of 5-cyano-uracil compounds and new intermediate products that can be formed thereby | |
US2804459A (en) | Preparation of 4-aminouracil | |
US2050169A (en) | High-molecular sulphur compounds and process of manufacturing the same | |
US2327213A (en) | Chemical compounds and process of preparing the same | |
GB1062563A (en) | Process for preparing 1-substiuted cycloheptimidazol-2(1h)-one compounds | |
US2344784A (en) | Method of preparing guanamines | |
US3127442A (en) | Method for preparing alkali salts of beta-alkylvinylsulfonates | |
GB985604A (en) | New compounds containing ethionylamino groups and process for preparing them | |
US3239526A (en) | 3-phenyl-4-aminocinnolines | |
GB735899A (en) | Manufacture of hydrazine compounds | |
SE304005B (en) | ||
US2359912A (en) | Sulphanilamide derivatives |