GB615254A - Improvements relating to the reclaiming of waste wax paper - Google Patents

Improvements relating to the reclaiming of waste wax paper

Info

Publication number
GB615254A
GB615254A GB1302146A GB1302146A GB615254A GB 615254 A GB615254 A GB 615254A GB 1302146 A GB1302146 A GB 1302146A GB 1302146 A GB1302146 A GB 1302146A GB 615254 A GB615254 A GB 615254A
Authority
GB
United Kingdom
Prior art keywords
acid
amino
wax
alkylol
glyoxalidines
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
GB1302146A
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.)
National Oil Products Co
Original Assignee
National Oil Products 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 National Oil Products Co filed Critical National Oil Products Co
Publication of GB615254A publication Critical patent/GB615254A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21CPRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C5/00Other processes for obtaining cellulose, e.g. cooking cotton linters ; Processes characterised by the choice of cellulose-containing starting materials
    • D21C5/02Working-up waste paper
    • D21C5/022Chemicals therefor
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/64Paper recycling

Abstract

Amino-amides having the general formula <FORM:0615254/IV(b)/1> where R1 represents an aliphatic chain containing at least 7 carbon atoms, R2 represents hydrogen or a 1 to 3 carbon atom alkylol group and n is 2 or 3 when R2 represents a hydrogen atom and is 1, 2 or 3 when R2 represents an alkylol group are prepared by reacting a suitable fat or fatty acid with a polyalkylene polyamine or with an alkylene or polyalkylene alkylol polyamine, generally at a temperature of from 150 DEG to 210 DEG C. The resulting amino-amides may be converted into glyoxalidines by heating at elevated temperature, e.g. about 300 DEG C., to drive off a molecule of water. The amino-amides and the glyoxalidines may be solubilized by treatment with an aliphatic monocarboxylic acid of 1 to 3 carbons, e.g. acetic, formic or glycollic acid or with a suitable ester of a mineral acid such as diethyl sulphate, triethyl phosphate or ethyl iodide forming soluble acid salts or alkylated derivatives respectively. The amino amides and glyoxalidines and the solubilized derivatives are utilized in the reclaiming of waste wax paper (see Group VIII). In examples: (1) hydrogenated soyabean oil and ethanol ethylene diamine are condensed in a closed vessel at 150 DEG C. for 6-8 hours and the product, believed to be an amino-amide, is solubilized by treatment with aqueous acetic acid; (2) peanut oil and diethylene triamine are similarly condensed to form an amino-amide; (3) the reactants of (2) are heated at between 180 DEG -190 DEG C. for 20 minutes and then the temperature is rapidly raised to 300 DEG C. to form the glyoxalidine. Other reagents mentioned are ethanol diethylene triamine and triethylene tetramine and generally any fatty acid or fatty acid glyceride having from 8 to 24 carbon atoms in the chain, e.g. oleic acid, ricinoleic acid, lauric acid, stearic acid and palmitic acid. Specification 524,847 is referred to.ALSO:Amino-amides having the general formula <FORM:0615254/IV (c)/1> where R1 represents an aliphatic chain containing at least 7 carbon atoms, R2 represents hydrogen or a 1-3 carbon atom alkylol group and n is 2 or 3 when R2 represents hydrogen and is 1, 2 or 3 when R2 represents an alkylol group, the glyoxalidines cyclized therefrom or solubilized derivatives, specifically, soluble acid salts or alkylated derivatives, of either are utilized in a process for reclaiming wax paper broke which comprises disintegrating the broke in water heated to a temperature sufficiently high to meet the wax constituent and adding one of the above mentioned compounds to the fibre and wax suspension to fix the wax on the fibre (see Group VIII). The preparation of the compounds is described (see Group IV (b)). Typical compounds are the amino amide obtained by reacting hydrogenated soyabean oil with ethanol ethylene diamine and the amino-amide and corresponding glyoxalidine obtained from peanut oil and diethylene triamine. Specification 524,847 is referred to.ALSO:Paper fibres, obtained by disintegrating waste wax-paper in water at a temperature sufficient to melt the wax, are wax-sized by adding a cationic surface active fixing agent which is an aminoamide having the general formula R1 CO (NH CH2 CH2) nNHR2, or the corresponding glyoxalidine or a solubilized quaternary derivative of either having additional radicals R2 and Z: R1 being an aliphatic chain with at least 7 C atoms; R2 being H or a 1 - 3C alkylol group; n being 2 or 3 when R2 is H or 1, 2 or 3 when R2 is alkylol; R3 being H or a 1 - 3C alkyl group, and Z the anion of a 1-3C aliphatic monocarboxylic or mineral acid. A cationic agent having the formula C17H35CONHC2H4NHC2H4OH, made by condensing hydrogenated soya bean oil with ethanol ethylene diamine may be used and an aliphatic monocarboxylic acid having 1-3C atoms, e.g. acetic acid may be added to attain pH.6. In the case of the glyoxalidines R1 may be a mixture of the alkyl radicals from peanut oil. Specification 524,847 and U.S.A. Specification 2,183,259 are referred to.
GB1302146A 1945-05-10 1946-04-30 Improvements relating to the reclaiming of waste wax paper Expired GB615254A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US59310445 US2488515A (en) 1945-05-10 1945-05-10 Utilization of waste wax paper

Publications (1)

Publication Number Publication Date
GB615254A true GB615254A (en) 1949-01-04

Family

ID=24373399

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1302146A Expired GB615254A (en) 1945-05-10 1946-04-30 Improvements relating to the reclaiming of waste wax paper

Country Status (4)

Country Link
US (1) US2488515A (en)
BE (2) BE478756A (en)
FR (1) FR926742A (en)
GB (1) GB615254A (en)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE466221A (en) * 1945-07-13
US2601671A (en) * 1946-10-23 1952-06-24 American Cyanamid Co Resin-impregnated leather board
US2686121A (en) * 1948-07-07 1954-08-10 Morton Chemical Co Process of loading cellulosic fibers
US2694633A (en) * 1950-02-23 1954-11-16 Talbott Dev Associates Affixing organic and inorganic additaments to cellulosic materials
US2745744A (en) * 1951-02-09 1956-05-15 Permacel Tape Corp Treating agents incorporation
US3021252A (en) * 1960-03-31 1962-02-13 Lawrence Paper Co Process of making wax-containing paper using waste wax paper
US3819470A (en) * 1971-06-18 1974-06-25 Scott Paper Co Modified cellulosic fibers and method for preparation thereof
DK150210C (en) * 1984-10-01 1987-06-22 Peter Dalkiaer PROCEDURE FOR THE PREPARATION OF A LIQUID-ABSORBING CUSHION, SPECIAL USE IN BLOOD HYGIENE ARTICLES AND SANITARY PRODUCTS
US4735682A (en) * 1985-02-21 1988-04-05 James River-Norwalk, Inc. Method for recovery of cellulosic fibers containing latex solids from latex bonded broke
US4997523A (en) * 1990-06-20 1991-03-05 Betz Panerchem, Inc. Method for effectively breaking up latex-coated paper during pulping to decrease the potential for white pitch deposition

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1793839A (en) * 1928-09-27 1931-02-24 Albert L Clapp Manufacture of waterproof fibrous products
US1970426A (en) * 1930-01-22 1934-08-14 Paten And Licensing Corp Paper making process
US1992589A (en) * 1931-04-17 1935-02-26 Dewey And Almy Chem Comp Organic fiber and method of preparing same
US2096129A (en) * 1936-02-24 1937-10-19 Bennett Inc Manufacture of sized papers
US2183259A (en) * 1937-03-03 1939-12-12 Nat Oil Prod Co Process for recovering and reusing constituents of waxed paper
US2186609A (en) * 1937-05-05 1940-01-09 Paper Chemistry Inst Method of removing wax from waxed paper stock
US2206090A (en) * 1937-05-17 1940-07-02 Warwick Chemical Co Waterproofing composition and similar emulsion
US2268273A (en) * 1939-05-27 1941-12-30 Carbide & Carbon Chem Corp Textile finishing
US2343090A (en) * 1940-08-03 1944-02-29 Du Pont Treatment of textiles and composition useful therefor
US2277788A (en) * 1940-08-03 1942-03-31 Du Pont Treatment of textiles and composition useful therefor
US2343095A (en) * 1940-08-03 1944-02-29 Du Pont Resin dispersion useful in the textile and paper industries
US2442972A (en) * 1941-01-23 1948-06-08 Sidney M Edelstein Aqueous dispersions of electropositive materials
US2347178A (en) * 1942-01-07 1944-04-25 Nat Oil Prod Co Reversible emulsion and application therefor
US2401027A (en) * 1942-10-21 1946-05-28 American Anode Inc Deposition of rubber from aqueous dispersions of rubber

Also Published As

Publication number Publication date
BE478756A (en) 1900-01-01
BE464980A (en) 1900-01-01
US2488515A (en) 1949-11-15
FR926742A (en) 1947-10-09

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