GB657419A - Improvements relating to the production of fatty polyamides - Google Patents
Improvements relating to the production of fatty polyamidesInfo
- Publication number
- GB657419A GB657419A GB6178/48A GB617848A GB657419A GB 657419 A GB657419 A GB 657419A GB 6178/48 A GB6178/48 A GB 6178/48A GB 617848 A GB617848 A GB 617848A GB 657419 A GB657419 A GB 657419A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- ethylene diamine
- oil
- acetic
- acetic anhydride
- 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
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
- D06M13/405—Acylated polyalkylene polyamines
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
- D01F2/06—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from viscose
- D01F2/08—Composition of the spinning solution or the bath
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/02—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/08—Amides
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/08—Amides
- C10M2215/082—Amides containing hydroxyl groups; Alkoxylated derivatives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/28—Amides; Imides
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/044—Polyamides
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/045—Polyureas; Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/46—Textile oils
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyamides (AREA)
Abstract
Mixed fatty polyamides derived from polyamines acylated with a carboxylic acid containing 8-22 carbon atoms and a carboxylic acid containing 2-5 carbon atoms (for preparation see Group IV (b)) may be added to viscose spinning baths to prevent clogging of the spinnerettes.ALSO:Mixed fatty polyamides are obtained by reacting a polyamine of formula <FORM:0657419/IV (b)/1> wherein n is a whole number, R3 is hydrogen or an alkylol radical and R4 and R5 is hydrogen or alkyl radicals with a fatty acid containing from 8 to 22, preferably 12 to 18, carbon atoms or an ester thereof and with a fatty acid containing from 2 to 5 carbon atoms or an ester, anhydride or acid halide thereof. Amines specified are ethylene diamine, diethylene triamine, triethylene tetramine, tetraethylene pentamine, and hydroxy ethyl ethylene diamine, diethylene triamine being preferred. It is preferred that the polyamide contains a secondary amino group for then solubility may be enhanced by treatment with weak acids, e.g. acetic and lactic acids, preferably by mixing a dilute aqueous solution of the acid with the molten polyamide, stirring until homogeneous, cooling and recovering the amide. When polyamines containing more than three nitrogen atoms are prepared it is preferred that sufficient amounts of short chain fatty acid are used to acylate all but one of the secondary amino groups. Long chain acids specified are caprylic, nonylic, capric, undecylic, lauric, myristic, palmitic, stearic, behenic, oleic and ricinoleic acids or mixtures thereof and as esters glycerides are mentioned and preferred to the free acid. Glycerides specified are teaseed, castor and hydrogenated castor oils. Short chain acids specified are acetic, glycollic, lactic, propionic, butyric or valeric acids. Acetic acid or anhydride is preferred. Preferably the long chain acid is first reacted with the polyamine although when using di- or triamines the short chain acid may be the first to be reacted. The long chain acid is reacted in equimolar proportions with the polyamine at approximately 120 DEG to 200 DEG C., preferably 150-170 DEG C. generally for about 8 hours. The pressure is preferably atmospheric although other pressures may be used. If a glyceride, e.g. coconut oil is used in place of the acid then approximately one-third mol. of the glyceride is used per mol. of polyamine. The monoamide is then mixed with the required amount of short chain acid or said derivative thereof and reaction effected at atmospheric or other pressure and at approximately 135 DEG C. for about 3 to 5 hours when the temperature is raised to 150 DEG to 170 DEG C. for about 5 to 8 additional hours. If desired, the free NH2 group may be completely acylated and the NH group adjacent the long chain fatty group may also be acylated. Generally the number of mols. of short chain acid employed per mol. of polyamine will be equivalent to the number of groups to be acylated. In examples in which reactions are effected at preferred temperatures acetic anhydride is used in each case in the second stage, the first stage being reactions between diethylene triamine and (1) and (2) coconut oil, (6) teaseed oil, (7) oleic acid, (8) palmitic acid, (9) lauric acid, and (10) stearic acid, and coconut oil is reacted with (3) tetraethylene pentamine, (4) ethylene diamine, and (5) hydroxy ethyl ethylene diamine, the products of all but (1), (4) and (5) being further treated with 3 per cent acetic acid by the method described above so as to increase their solubility in water. In the Specification as open to inspection under Sect. 91 the amines to be used may contain ether, keto, imino, neutralized imino, hydroxyl and amide groups in the portion of the molecule between the amino groups and an acid chloride of the long chain acid may be used. Many other polyamines are specified, e.g. sym. diamino ethyl ether, 1,6-diamino hexane and particularly those containing hydroxy groups such as ethanol propylene diamine, 1-amino-3-methyl amino isopropanol and 1 - amino - dimethyl - 5 - methylaminodimethyl n-pentanol-3. In examples ethylene diamine is reacted with (11) hydrogenated tallow and glycollic acid, and (12) oleic acid and acetic anhydride, (13) sym. diethyl ethylene diamine is reacted with stearic acid and lactic acid, ethanol ethylene diamine is reacted with (14) hydrogenated soyabean oil and acetic acid, (15) stearic acid and acetic anhydride, (16) oleic acid and acetic anhydride, (17) refined corn oil and acetic anhydride, (18) lauric acid chloride and glyceric acid and (19) oleic acid and glycollic acid and in (20) 1,3-diamino isopropanol is reacted with stearic acid and acetic anhydride. This subject-matter does not appear in the Specification as accepted.ALSO:Textile softeners and wetting and dispersing agents comprise mixed fatty polyamides derived from polyamides acylated with a carboxylic acid containing 8-22 carbon atoms and a carboxylic acid containing 2-5 carbon atoms (for preparation see Group IV (b)). The polyamides are also stated to be of use in the preparation of detergents. They may be applied to the material in the form of dilute solutions. In the Specification as open to inspection under Sect. 91 an example (21) is given in which cotton sheeting is passed through a quetch containing a 1/4 per cent aqueous dispersion of a polyamide derived from ethanol ethylene diamine, coconut oil and acetic anhydride, the fabric having a smooth, soft and even handle when dried. This subject-matter does not appear in the Specification as accepted.ALSO:Mixed fatty polyamides derived from polyamines acylated with a carboxylic acid containing 8-22 carbon atoms and a carboxylic acid containing 2-5 carbon atoms (for preparation see Group IV (b)) are lubricants for textiles and other fibrous materials and are used as defoamers and in the preparation of emulsifying agents. In the Specification as open to inspection under Sect. 91, examples are given: (14) of an emulsifying agent obtained from hydrogenated soya bean oil, acetic acid and ethanol ethylene diamine; (17) of a water-in-oil emulsifying agent from refined corn oil, acetic anhydride and ethanol ethylene diamine; (22) an emulsion for waterproofing textiles is obtained by melting together paraffin wax and the amide of (14) and adding thereto aqueous aluminium acetate solution; (23) a condensation product derived from ethanol ethylene diamine, oleic acid and acetic anhydride is used to form a water-in-oil emulsion of mineral seal oil; (25) an emulsion is obtained from neats' foot oil, water and a hydroxy acetic acid solution of the product of (17); (18) the product of reaction between ethanol ethylene diamine, lauric acid chloride and glyceric acid is said to show excellent lubricating properties and that of (19) derived from the same amine, oleic acid and glycollic acid is said to have fibre lubricating properties. This subject-matter does not appear in the Specification as accepted.ALSO:The Specification as open to inspection under Sect. 91 contains an example (23) of a lubricant for use in the moulding of ceramic materials comprising a water-in-oil emulsion of mineral seal oil, the emulsifying agent being a mixed fatty polyamide derived from ethanol ethylene diamine (1 mol.), stearic acid (1 mol.) and acetic anhydride ( 1/2 mol.). For the preparation of this and similar amides (see Group IV (b)). This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US274808A US2345632A (en) | 1939-05-20 | 1939-05-20 | Polyamides |
Publications (1)
Publication Number | Publication Date |
---|---|
GB657419A true GB657419A (en) | 1951-09-19 |
Family
ID=23049692
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB6178/48A Expired GB657419A (en) | 1939-05-20 | 1948-02-27 | Improvements relating to the production of fatty polyamides |
Country Status (2)
Country | Link |
---|---|
US (1) | US2345632A (en) |
GB (1) | GB657419A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2946746A (en) * | 1956-10-01 | 1960-07-26 | Union Oil Co | Oil-external emulsion drilling fluids |
US3122504A (en) * | 1956-04-18 | 1964-02-25 | Bohme Fellchemie G M B H | Condensation products of polyalkylenepolyamines and esters of high molecular carboxylic acids |
DE1201805B (en) * | 1959-06-16 | 1965-09-30 | Ciba Geigy | Process for softening textile materials |
GB2209533A (en) * | 1987-09-29 | 1989-05-17 | Shri Ram Fibres Ltd | Treating leather |
EP0911384A2 (en) * | 1997-10-22 | 1999-04-28 | Polygon Chemie AG | Conveyor lubricant |
Families Citing this family (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2425392A (en) * | 1939-05-20 | 1947-08-12 | Nopco Chem Co | Diamide textile lubricants |
US2425393A (en) * | 1939-05-20 | 1947-08-12 | Nopco Chem Co | Hydroxylated polyamide textile lubricants |
US2580880A (en) * | 1942-03-27 | 1952-01-01 | Nat Aluminate Corp | Prevention of foaming in steam generation |
US2580922A (en) * | 1942-09-19 | 1952-01-01 | Nat Aluminate Corp | Prevention of foaming in steam generation |
US2419404A (en) * | 1943-03-09 | 1947-04-22 | Nostrip Inc | Method for higher fatty acid polyamine soaps |
US2427481A (en) * | 1943-11-01 | 1947-09-16 | Lockheed Aircraft Corp | Water-thinned paints |
US2485378A (en) * | 1943-12-08 | 1949-10-18 | Dearborn Chemicals Co | Method of inhibiting foaming in steam boilers |
US2534441A (en) * | 1945-03-19 | 1950-12-19 | Dearborn Chemicals Co | Method of and composition for inhibiting foaming in steam boilers |
US2525770A (en) * | 1946-05-17 | 1950-10-17 | Arkansas Company Inc | Baths for stripping vat-dyed textile materials and agents useful therein |
US2462358A (en) * | 1946-06-21 | 1949-02-22 | Eastman Kodak Co | Amides of acetoacetic acid and process for their preparation |
US2496776A (en) * | 1946-06-21 | 1950-02-07 | Eastman Kodak Co | Textile yarns impregnated with lubricating compositions |
BE474161A (en) * | 1946-06-28 | |||
US2588343A (en) * | 1946-12-21 | 1952-03-11 | Nat Aluminate Corp | Inhibiting foaming in steam generators |
US2717881A (en) * | 1946-12-21 | 1955-09-13 | Nat Aluminate Corp | Inhibition of foaming in steam generators |
US2528274A (en) * | 1947-09-09 | 1950-10-31 | Dearborn Chemicals Co | Amide composition |
US2600361A (en) * | 1948-06-09 | 1952-06-10 | Dearborn Chemicals Co | Prevention of foaming in steam generation |
US2727836A (en) * | 1949-08-01 | 1955-12-20 | American Viscose Corp | Anti-sticking cellulose pellicles and method of making |
US2622018A (en) * | 1949-10-19 | 1952-12-16 | Socony Vacuum Oil Co Inc | Motor fuel |
US2638449A (en) * | 1949-12-30 | 1953-05-12 | Socony Vacuum Oil Co Inc | Reaction products of fatty acids, dialkanolamines, and alkenyl succinic acid anhydrides |
US2811495A (en) * | 1952-06-20 | 1957-10-29 | Gen Mills Inc | Mixed suspensoids of epoxy resins and polyamide resins |
US2811459A (en) * | 1953-10-16 | 1957-10-29 | Gen Mills Inc | Polyamide suspensoids forming continuous films |
US2805135A (en) * | 1954-08-25 | 1957-09-03 | Eastman Kodak Co | Stabilized hydrocarbon fuel oil compositions and stabilizaers therefor |
US2914417A (en) * | 1956-08-07 | 1959-11-24 | Nat Aluminate Corp | Treatment of hydrocarbon liquids |
NL262139A (en) * | 1961-03-08 | 1900-01-01 | ||
US3169980A (en) * | 1961-03-31 | 1965-02-16 | California Research Corp | Fatty acid polyamide |
US3394799A (en) * | 1964-09-08 | 1968-07-30 | American Cyanamid Co | Adhesive tape carrying release coating |
US3387993A (en) * | 1964-10-16 | 1968-06-11 | Ampex | Magnetic tape with a lubricant containing mineral oil and fatty acid amide in the magnetic coating |
US4269606A (en) * | 1976-08-13 | 1981-05-26 | Phillips Petroleum Company | Fuel and lubricant additives from acid treated mixtures of vegetable oil derived amides and esters |
US4344771A (en) * | 1978-08-23 | 1982-08-17 | Phillips Petroleum Company | Fuel and lubricant additives from acid treated mixtures of vegetable oil derived amides and esters |
US4504280A (en) * | 1983-08-17 | 1985-03-12 | Phillips Petroleum Company | Fuel additives from SO2 treated mixtures of amides and esters derived from vegetable oil, tall oil acid, or aralkyl acid |
FR2772783A1 (en) * | 1997-12-24 | 1999-06-25 | Elf Antar France | New additives compositions for improving the lubricating power of low sulfur petrol, diesel and jet fuels |
FR2772784B1 (en) * | 1997-12-24 | 2004-09-10 | Elf Antar France | ONCTUOSITY ADDITIVE FOR FUEL |
US20050276960A1 (en) * | 2004-06-15 | 2005-12-15 | Lee Jerry H C | Fatty amide composition for wet use chopped strand glass fibers |
-
1939
- 1939-05-20 US US274808A patent/US2345632A/en not_active Expired - Lifetime
-
1948
- 1948-02-27 GB GB6178/48A patent/GB657419A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3122504A (en) * | 1956-04-18 | 1964-02-25 | Bohme Fellchemie G M B H | Condensation products of polyalkylenepolyamines and esters of high molecular carboxylic acids |
US2946746A (en) * | 1956-10-01 | 1960-07-26 | Union Oil Co | Oil-external emulsion drilling fluids |
DE1201805B (en) * | 1959-06-16 | 1965-09-30 | Ciba Geigy | Process for softening textile materials |
GB2209533A (en) * | 1987-09-29 | 1989-05-17 | Shri Ram Fibres Ltd | Treating leather |
EP0911384A2 (en) * | 1997-10-22 | 1999-04-28 | Polygon Chemie AG | Conveyor lubricant |
EP0911384A3 (en) * | 1997-10-22 | 1999-06-16 | Polygon Chemie AG | Conveyor lubricant |
Also Published As
Publication number | Publication date |
---|---|
US2345632A (en) | 1944-04-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB657419A (en) | Improvements relating to the production of fatty polyamides | |
US2103872A (en) | Higr molecular nitrogenous organic compounds containing carboxylic groups | |
US2993887A (en) | Anhydro amides | |
US2528378A (en) | Metal salts of substituted quaternary hydroxy cycloimidinic acid metal alcoholates and process for preparation of same | |
US2425392A (en) | Diamide textile lubricants | |
US2880219A (en) | Production of n-acyl taurides | |
US2176896A (en) | Quaternary ammonium derivatives of amides | |
US2187823A (en) | Condensation products of ethers of alkylol amines | |
US2206928A (en) | Production of condensation products | |
GB524847A (en) | Improvements in or relating to oil compositions | |
US2484146A (en) | Lubricating composition | |
JPS6323314B2 (en) | ||
US2372797A (en) | Condensation products | |
US2268395A (en) | Quaternary ammonium compounds | |
US1952008A (en) | Emulsifying detergent and wetting agent | |
US3389145A (en) | Fatty oxazoline surfactants and a process for their preparation | |
US1947951A (en) | Acidyl polyalkylene polyamines | |
US2525771A (en) | Fatty acid-aliphatic amine polyglycol combinations useful as textile assistants and process of producing the same | |
US2425393A (en) | Hydroxylated polyamide textile lubricants | |
US2338178A (en) | Condensation product | |
US2491478A (en) | Polyalcohol-fatty acid-aliphatic amine combinations useful as textile assistants andprocess of producing the same | |
US2190133A (en) | Quaternary ammonium derivatives of alcohol amine compounds | |
CH321110A (en) | Process for the production of nitrogen-containing condensation products | |
JPH07116675B2 (en) | Method for producing softener composition | |
US2765324A (en) | Surface active polycarbamates |