GB418919A - Improvement in pickling compounds - Google Patents

Improvement in pickling compounds

Info

Publication number
GB418919A
GB418919A GB16044/33A GB1604433A GB418919A GB 418919 A GB418919 A GB 418919A GB 16044/33 A GB16044/33 A GB 16044/33A GB 1604433 A GB1604433 A GB 1604433A GB 418919 A GB418919 A GB 418919A
Authority
GB
United Kingdom
Prior art keywords
chloride
bases
bromide
nitrogen
heterocyclic
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
Application number
GB16044/33A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Barrett Co Inc
Original Assignee
Barrett Co Inc
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 Barrett Co Inc filed Critical Barrett Co Inc
Publication of GB418919A publication Critical patent/GB418919A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C23GCLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
    • C23G1/00Cleaning or pickling metallic material with solutions or molten salts
    • C23G1/02Cleaning or pickling metallic material with solutions or molten salts with acid solutions
    • C23G1/04Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors
    • C23G1/06Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors organic inhibitors

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

The corrosion of a metal in an acid bath is inhibited by providing the bath with a corrosion inhibitor obtained by reacting a heterocyclic nitrogen base, the heterocyclic rings of which consist of carbon and nitrogen atoms with an organic sulphonic acid ester containing an aryl group or an organic halide containing an aryl group. 1 to 3 mols. of base may be reacted with one mol. of the halide or the sulphonic acid ester. The reaction probably produces a quaternary ammonium compound. The nitrogen bases referred to are polyatomic-carbon heterocyclic bases containing one or more trivalent nitrogen atoms in the heterocyclic nucleus, e.g. pyridines, quinolines, acridines, or their derivatives, or commercial materials containing such compounds such as denaturing or flotation pyridines, bone oils or the like. Crude pyridine consisting of a coal tar base distillate boiling between 217 and 346 DEG C. at atmospheric pressure may be employed or bases derived therefrom by fractional distillation under reduced pressure. Methyl-para-toluene sulphonate is given as a suitable sulphonic ester and benzyl chloride, benzal chloride, benzotrichloride, benzyl bromide, phenyl ethyl chloride, phenyl ethyl bromide, orthochlorbenzyl chloride, paranitrobenzyl bromide, benzoyl chloride, benzoyl bromide, m-nitrobenzoyl chloride, para-nitrobenzoyl chloride and chloroacetophenone are given as suitable halides. Any halide may be employed having an aromatic nucleus consisting of one or more carbocyclic or heterocyclic rings, with or without substituents such as --NH2, --NO2, --HSO3, --Cl, --Br, --I, --CN, or --OH and whose aliphatic side chain contains one or more carbon atoms to which one or more halogen atoms are attached, which aliphatic chains may be partially or completely saturated with hydrogen and oxygen atoms. According to an example, a mixture of benzyl chloride and high boiling pyridine bases is heated under a reflux condenser to 130 DEG C. the reaction subsequently raising the temperature to 160--170 DEG C. After cooling, the product or the other inhibitors according to the invention may be diluted with one of the following solvents, namely, denatured alcohol, high-boiling pyridine bases, aqueous hydrochloric acid, aqueous sulphuric acid, a mixture of alcohol and aqueous hydrochloric acid or a mixture of pyridine bases and aqueous hydrochloric acid. The resulting solutions may be diluted with water to precipitate tarry matter and then decanted. A pickling bath for iron and steel may contain 2--15 per cent mineral, e.g. sulphuric acid, and about 0,1 per cent of the above reaction product added either alone or in the form of one of the above solutions. A pickling temperature of 50--95 DEG C. may be employed. The Specification as open to inspection under Sect. 91 describes also the production of inhibitors by reacting organic nitrogen bases with alkyl halides or alkyl sulphonates. This subject-matter does not appear in the Specification as accepted.ALSO:Quaternary ammonium compounds, for use in reducing the corrosion of a metal in an acid bath, are obtained by reacting a heterocyclic nitrogen base with an organic sulphonic acid ester containing an aryl group or with an organic halide containing an aryl group. From 1 to 3 mols. of base may be reacted with one mol. of the halide or the sulphonic acid ester. The nitrogen bases specified are pyridines, quinolines, and acridines or their derivatives, or commercial materials containing such compounds such as denaturing or flotation pyridines or bone oils. Crude pyridine consisting of a coal tar base distillate boiling between 217 and 346 DEG C. at atmospheric pressure may be employed or bases derived therefrom by fractional distillation under reduced pressure. Methyl-p-toluene sulphonate is given as a suitable sulphonic ester and benzyl chloride, benzal chloride, benzotrichloride, benzyl bromide, phenyl ethyl chloride, phenyl ethyl bromide, o-chlorbenzyl chloride, p-nitrobenzyl bromide, benzoyl chloride, benzoyl bromide, m-nitrobenzoyl chloride, p-nitrobenzoyl chloride and chloracetophenone are given as suitable halides. Any halide may be employed having an aromatic nucleus consisting of one or more carbocyclic or heterocyclic rings, with or without substituents such as --NH2, --NO2, --HSO3, --C1, --Br, --I, --CN, or --OH, and an aliphatic side chain containing one or more carbon atoms to which one or more halogen atoms may be attached. In an example, a mixture of benzyl chloride and high boiling pyridine bases is heated under a reflux condenser to 130 DEG C. the reaction subsequently raising the temperature to 160--170 DEG C. The Specification as open to inspection under Sect. 91 describes p also the production of inhibitors by reacting organic nitrogen bases with alkyl halides or alkyl sulphonates. This subject-matter does not appear in the Specification as accepted.ALSO:The corrosion of a metal in an acid bath is inhibited by providing the bath with a corrosion inhibitor obtained by reacting a heterocyclic nitrogen base, the heterocyclic rings of which S consist of carbon and nitrogen atoms, with an organic sulphonic acid ester containing an aryl group or an organic halide containing an aryl group. 1 to 3 mols. of base may be reacted with one mol. of the halide or the sulphonic acid ester. The reaction probably produces a quaternary ammonium compound. The nitrogen bases referred to are polyatomic-carbon heterocyclic bases containing one or more tri-valent nitrogen atoms in the heterocyclic nucleus, e.g. pyridines, quinolines, acridines, or their derivatives, or commercial materials containing such compounds such as denaturing or flotation pyridines, bone oils or the like. Crude pyridine consisting of a coal tar base distillate boiling between 217 and 346 DEG C. at atmospheric pressure may be employed or bases derived therefrom by fractional distillation under reduced pressure. Methyl-paratoluene sulphonate is given as a suitable sulphonic ester and benzyl chloride, benzal chloride, benzotrichloride, benzyl bromide, phenyl ethyl chloride, phenyl ethyl bromide, orthochlorbenzyl chloride, para-nitrobenzyl bromide, benzoyl chloride, benzoyl bromide, m - nitrobenzoyl chloride, para - nitrobenzoyl chloride and chloroacetophenone are given as suitable halides. Any halide may be employed having an aromatic nucleus consisting of one or more carbocyclic or heterocyclic rings, with or without substituents such as -NH2, -NO2, -HSO3, -Cl, -Br, -I, -CN, or -OH and whose aliphatic side chain contains one or more carbon atoms to which one or more halogen atoms are attached, which aliphatic chains may be partially or completely saturated with hydrogen and oxygen atoms. According to an example, a mixture of benzyl chloride and high boiling pyridine bases is heated under a reflux condenser to 130 DEG C. the reaction subsequently raising the temperature to 160-170 DEG C. After cooling, the product or the other inhibitors according to the invention may be diluted with one of the following solvents, namely, denatured alcohol, high-boiling pyridine bases, aqueous hydrochloric acid, aqueous sulphuric acid, a mixture of alcohol and aqueous hydrochloric acid or a mixture of pyridine bases and aqueous hydrochloric acid. The resulting solutions may be diluted with water to precipitate tarry matter and then decanted. A pickling bath for iron and steel may contain 2-15 per cent mineral, e.g. sulphuric, acid and about 0,1 per cent of the above reaction product added either alone or in the form of the above solutions. A pickling temperature of 50-95 DEG C. may be employed. The Specification as open to inspection under Sect. 91 describes also the production of inhibitors by reacting organic nitrogen bases with alkyl halides or alkyl sulphonates. This subject-matter does not appear in the Specification as accepted.
GB16044/33A 1932-06-02 1933-06-02 Improvement in pickling compounds Expired GB418919A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US615024A US2037762A (en) 1932-06-02 1932-06-02 Pickling compound and method of making and using same

Publications (1)

Publication Number Publication Date
GB418919A true GB418919A (en) 1934-11-02

Family

ID=24463694

Family Applications (1)

Application Number Title Priority Date Filing Date
GB16044/33A Expired GB418919A (en) 1932-06-02 1933-06-02 Improvement in pickling compounds

Country Status (3)

Country Link
US (1) US2037762A (en)
FR (1) FR756425A (en)
GB (1) GB418919A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2955087A (en) * 1957-04-08 1960-10-04 Arthur D Berryman Compositions and methods for treating metal surfaces

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2814593A (en) * 1953-12-18 1957-11-26 Gen Aniline & Film Corp Corrosion inhibition
US3135632A (en) * 1957-05-24 1964-06-02 William R Lucas Method of protecting ferrous metal surfaces from rerusting
US3249548A (en) * 1958-10-31 1966-05-03 Cumberland Chemical Corp Corrosion inhibiting composition comprising 4-ethyl-1-octyn-3-ol
US3111492A (en) * 1958-11-06 1963-11-19 Onyx Chemical Corp Chemical treatment of flood waters used in secondary oil recovery
US3019081A (en) * 1959-07-17 1962-01-30 Phillips Petroleum Co Stabilized nitric acid
US3096341A (en) * 1960-04-25 1963-07-02 United States Steel Corp 9-cyanoethyl dodecahydrocarbazole
AT325373B (en) * 1973-02-07 1975-10-27 Boehm Franz Chem Prod METHOD FOR PREVENTING THE ZINC ATTACK OF A CALCULATING ACID ON GALVANIZED IRON
US4028268A (en) * 1975-12-03 1977-06-07 Exxon Research And Engineering Company High temperature corrosion inhibitor
US5009799A (en) * 1988-02-16 1991-04-23 Nalco Chemical Company Inorganic acid solution viscosifier and corrosion inhibitor and method
USH751H (en) 1988-06-10 1990-03-06 Sullivan Daniel S Method of inhibiting acid corrosion of ferrous metals

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2955087A (en) * 1957-04-08 1960-10-04 Arthur D Berryman Compositions and methods for treating metal surfaces

Also Published As

Publication number Publication date
US2037762A (en) 1936-04-21
FR756425A (en) 1933-12-09

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