GB466344A - Improvements in the manufacture and production of nitrogenous products - Google Patents
Improvements in the manufacture and production of nitrogenous productsInfo
- Publication number
- GB466344A GB466344A GB824937A GB824937A GB466344A GB 466344 A GB466344 A GB 466344A GB 824937 A GB824937 A GB 824937A GB 824937 A GB824937 A GB 824937A GB 466344 A GB466344 A GB 466344A
- Authority
- GB
- United Kingdom
- Prior art keywords
- treated
- products
- ethyleneimine
- product
- reacted
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/0206—Polyalkylene(poly)amines
- C08G73/0213—Preparatory process
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Assistants useful in the textile, leather, lacquer, rubber, pharmaceutical, and cosmetic industries are obtained when mono or polymeric 1 : 2-alkyleneimines are condensed with aliphatic alcohols or oxides or esters thereof, other than carboxylic acid esters. The treatment of monomeric ethyleneimine or N-methylethyleneimine with methyliodide is also excluded. The reaction may be combined with a condensation with (a) aldehydes and ketones, (cf. Specification 466,346); (b) halogenated aromatic compounds and aromatic sulphonic halides, (cf. Specification 466,345), or (c) other substances capable of condensation, e.g. urea or its substitution products such as dimethylolurea, thiourea, phenols, cetylamine, octodecylamine or other amine or styrene, synthetic rubber or synthetic resins. The condensation may be effected in the presence of solvents or diluents such as water, alcohol, ether, cyclohexanone, toluene, carbontetrachloride or chlorbenzene. Acyl, sulphonic, sulphuric ester, carboxylic or phosphoric acid groups may be introduced into the products or into the reacting components. The products may be added in dyeing, printing, dressing, stripping, fulling, levelling, tanning, washing, dispersing and wetting processes. They may also be used in softening and flotation agents and to increase the affinity of viscose or copper artificial silk for acid dyestuffs. They may be added to spinning solutions and the products obtained with the co-employment of aldehydes or ketones may be used for dressing textiles, leather, paper or straw and for rendering artificial silk crease and slide proof. Dispersing agents such as sulphuric esters of fatty alcohols and aliphatic sulphonic acids may be used with the products, which can also be employed in the form of salts with mineral or organic, e.g. fatty acids. In examples: (1) polymerized ethyleneimine is treated with the alkyl bromides corresponding to palm kernel fatty acids; the products may be treated with chlorsulphonic acid or phosphorus oxychloride to render them soluble; a textile fabric is treated with a solution of the product in a solvent and then passed into a bath of formaldehyde: a resin is produced by treating the product with excess formaldehyde; (2) polymerized ethyleneimine or its reaction product with b : b <1>-dichlordiethylether is reacted with stearylisocyanate; the reaction may be carried out on a textile fibre; the product may be treated with chlorethanesulphonic acid or chlorsulphonic acid; (3) ethyleneimine is reacted with benzylchloride or the alkylbromides derived from palm kernel oil and the product treated with ethyleneoxide; (4) propylethyleneimine is reacted with epichlorhydrin; the product is a preservative against moths; (5) polymerized ethyleneimine is treated with a chlorinated paraffin wax; the product may be reacted with benzylchloride, dimethylsulphate; or ethyleneoxide to obtain further products which may be added to viscose or copper artificial silk spinning solutions; (6) polymeric C-butyleneimine is treated with sodium chlorethanesulphonate; and the product condensed with butyl, hexyl, octodecenyl chloride or octodecyl bromide; (7) polymeric propyl or phenylethyleneimine is reacted with monoglycerol chlorhydrin; by introducing high molecular aliphatic radicles, e.g. by means of dodecyl bromide, products having a water repelling action are obtained; (8) polymeric butyl, hexyl or dodecylethyleneimine is treated with ethylene or propylene oxide, or glycide; (9) N-phenyl, benzyl or cyclohexylethyleneimine is treated with ethylene oxide to obtain a levelling agent having disinfecting action; (10) ethyl or butyl ethyleneimine is reacted with ethyleneoxide to obtain a product suitable for adding to viscose and copper artificial silk spinning baths; (11) polymeric ethyleneimine is treated first with ethylene oxide and then with sodium benzyl chloride sulphonate. Methylethyleneimine and o -chlor-a : b -butyleneimine are specified and the use of dichloroctodecane and butylene oxide is mentioned.ALSO:Products which may be added to preparations used as dispersing agents are obtained when mono or polymeric 1 : 2-alkyleneimines are condensed with aliphatic alcohols or oxides or esters thereof--other than carboxylic acid esters. The treatment of monomeric ethyleneimine of N-methylethyleneimine with methyliodide is also excluded. The reaction may be combined with a condensation with (a) aldehydes and ketones, cf. Specification 466,346, (b) halogenated aromatic compounds and aromatic sulphonic halides, cf. Specification 466,345, or (c) other substances capable of condensation, e.g. urea or its substitution products such as dimethylolurea, thiourea, phenols, cetylamine, octodecylamine or other amine or styrene, synthetic rubber or synthetic resins. Acyl, sulphonic, sulphuric ester, carboxylic, or phosphonic acid groups may be introduced into the products or into the reacting components. Dispersing agents such as sulphuric esters of fatty alcohols and aliphatic sulphonic acids may be used with the products, which can also be employed in the form of salts with mineral or organic, e.g. fatty acids. In examples: (1) polymerized ethyleneimine is treated with the alkyl bromides corresponding to palm kernel fatty acids; the products may be treated with chlorsulphonic acid or phosphorus oxychloride to render them soluble; a resin is produced by heating the product with excess formaldehyde; (2) polymerized ethyleneimine or its reaction product with b : b -dichlordiethylether is reacted with stearylisocyanate; the product may be treated with chlorethanesulphonic acid or chlorsulphonic acid; (3) ethyleneimine is reacted with benzylchloride or the alkylbromides derived from palm kernel oil and the product treated with ethyleneoxide; (4) propylethyleneimine is reacted with epichlorhydrin; (5) polymerized ethyleneimine is treated with a chlorinated paraffin wax; the product may be reacted with benzylchloride, dimethylsulphate or ethyleneoxide to obtain further products; (6) polymeric C-butyleneethyleneimine is treated with sodium chlorethanesulphonate; and the product condensed with butyl, hexyl or octodecenyl chloride or octodecyl bromide; (7) polymeric propyl or phenylethyleneimine is reacted with monoglycerol chlorhydrin; by introducing high molecular aliphatic radicles, e.g. by means of dodecyl bromide, further products are obtained; (8) polymeric butyl, hexyl or dodecyl ethyleneimine is treated with ethylene or propylene oxide or glycide; (9) N-phenyl, benzyl or cyclohexylethyleneimine is treated with ethylene oxide; (10) ethyl or butyl ethyleneimine is reacted with ethyleneoxide; (11) polymeric ethyleneimine is treated first with ethylene oxide and then with sodium benzyl chloride suphonate. Methylethyleneimine and o -chlor-a : b -butyleneimine are specified, and the use of dichloroctodecane and butylene oxide is mentioned.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB824937A GB466344A (en) | 1935-08-22 | 1935-08-22 | Improvements in the manufacture and production of nitrogenous products |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB824937A GB466344A (en) | 1935-08-22 | 1935-08-22 | Improvements in the manufacture and production of nitrogenous products |
Publications (1)
Publication Number | Publication Date |
---|---|
GB466344A true GB466344A (en) | 1937-05-24 |
Family
ID=9848869
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB824937A Expired GB466344A (en) | 1935-08-22 | 1935-08-22 | Improvements in the manufacture and production of nitrogenous products |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB466344A (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2475068A (en) * | 1944-03-25 | 1949-07-05 | Carbide & Carbon Chem Corp | Hydroxyalkyl alkylenimines and method of making same |
US2479480A (en) * | 1946-04-18 | 1949-08-16 | American Cyanamid Co | Fatty acid condensation products of water-soluble thermoplastic amine resins |
US2626931A (en) * | 1948-10-01 | 1953-01-27 | Hoechst Ag | Polymerization products and process of preparing them |
DE1004614B (en) * | 1954-06-26 | 1957-03-21 | Basf Ag | Process for the production of nitrogenous addition compounds |
US3224940A (en) * | 1961-12-18 | 1965-12-21 | Lilly Co Eli | Antacid compositions and method of using same |
US3240720A (en) * | 1960-04-22 | 1966-03-15 | Minnesota Mining & Mfg | Bifunctional monomers and process for their production |
US3247185A (en) * | 1963-03-20 | 1966-04-19 | Dow Chemical Co | Certain alkenylaziridines and their preparation |
US3257249A (en) * | 1963-06-06 | 1966-06-21 | Thiokol Chemical Corp | Method of making acetylenic epoxy amino compounds |
US3310460A (en) * | 1963-12-31 | 1967-03-21 | Chemirad Corp | Sizing composition of starch and a reaction product of an isocyanate with an alkylene imine and process of sizing paper therewith |
US3332841A (en) * | 1961-10-04 | 1967-07-25 | Lilly Co Eli | Method of treating hyperacidity |
US3354103A (en) * | 1964-04-06 | 1967-11-21 | Le Roy A White | Sequestering ion exchange resins which are polyimine reaction products |
US4032480A (en) * | 1975-07-11 | 1977-06-28 | David Solomonovich Zhuk | Method of producing linear polyethylenimine |
GB2180249A (en) * | 1982-12-23 | 1987-03-25 | Procter & Gamble | Ethoxylated polyamino compounds |
-
1935
- 1935-08-22 GB GB824937A patent/GB466344A/en not_active Expired
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2475068A (en) * | 1944-03-25 | 1949-07-05 | Carbide & Carbon Chem Corp | Hydroxyalkyl alkylenimines and method of making same |
US2479480A (en) * | 1946-04-18 | 1949-08-16 | American Cyanamid Co | Fatty acid condensation products of water-soluble thermoplastic amine resins |
US2626931A (en) * | 1948-10-01 | 1953-01-27 | Hoechst Ag | Polymerization products and process of preparing them |
DE1004614B (en) * | 1954-06-26 | 1957-03-21 | Basf Ag | Process for the production of nitrogenous addition compounds |
US3240720A (en) * | 1960-04-22 | 1966-03-15 | Minnesota Mining & Mfg | Bifunctional monomers and process for their production |
US3332841A (en) * | 1961-10-04 | 1967-07-25 | Lilly Co Eli | Method of treating hyperacidity |
US3224940A (en) * | 1961-12-18 | 1965-12-21 | Lilly Co Eli | Antacid compositions and method of using same |
US3247185A (en) * | 1963-03-20 | 1966-04-19 | Dow Chemical Co | Certain alkenylaziridines and their preparation |
US3257249A (en) * | 1963-06-06 | 1966-06-21 | Thiokol Chemical Corp | Method of making acetylenic epoxy amino compounds |
US3310460A (en) * | 1963-12-31 | 1967-03-21 | Chemirad Corp | Sizing composition of starch and a reaction product of an isocyanate with an alkylene imine and process of sizing paper therewith |
US3354103A (en) * | 1964-04-06 | 1967-11-21 | Le Roy A White | Sequestering ion exchange resins which are polyimine reaction products |
US4032480A (en) * | 1975-07-11 | 1977-06-28 | David Solomonovich Zhuk | Method of producing linear polyethylenimine |
GB2180249A (en) * | 1982-12-23 | 1987-03-25 | Procter & Gamble | Ethoxylated polyamino compounds |
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