GB657419A - Improvements relating to the production of fatty polyamides - Google Patents

Improvements relating to the production of fatty polyamides

Info

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
Application number
GB6178/48A
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.)
Nopco Chemical Co
Original Assignee
Nopco Chemical Co
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 Nopco Chemical Co filed Critical Nopco Chemical Co
Publication of GB657419A publication Critical patent/GB657419A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating 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
    • D06M13/402Amides imides, sulfamic acids
    • D06M13/405Acylated polyalkylene polyamines
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F2/00Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
    • D01F2/06Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from viscose
    • D01F2/08Composition of the spinning solution or the bath
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/02Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/08Amides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/08Amides
    • C10M2215/082Amides containing hydroxyl groups; Alkoxylated derivatives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/28Amides; Imides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/04Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/044Polyamides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/04Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/045Polyureas; Polyurethanes
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/46Textile 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.
GB6178/48A 1939-05-20 1948-02-27 Improvements relating to the production of fatty polyamides Expired GB657419A (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Cited By (6)

* Cited by examiner, † Cited by third party
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

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