GB815830A - Sizing nylon yarns - Google Patents
Sizing nylon yarnsInfo
- Publication number
- GB815830A GB815830A GB27140/56A GB2714056A GB815830A GB 815830 A GB815830 A GB 815830A GB 27140/56 A GB27140/56 A GB 27140/56A GB 2714056 A GB2714056 A GB 2714056A GB 815830 A GB815830 A GB 815830A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ethylene
- carbon atoms
- alcohols
- alkyl group
- maleic 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
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
- Y10T428/2967—Synthetic resin or polymer
- Y10T428/2969—Polyamide, polyimide or polyester
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Water-soluble sizes for application to nylon fibres are produced by interpolymerizing ethylene and maleic anhydride and hydrolysing the polymer to a free acid form or reacting it with an alcohol to form an acid ester, or by interpolymerizing ethylene with a maleic acid half ester, to which polymerization mix may be added maleic anhydride. The ester groups may be obtained from aliphatic saturated monohydric alcohols having up to 20 carbon atoms which may be primary, secondary or tertiary, straight or branched chain, chloro- or nitro-substituted or unsaturated alcohols or ether alcohols produced from ethylene oxide and low M.W. aliphatic alcohols. The polymerization may be effected at raised temperatures and under high pressures. An excess of ethylene above equimolecular proportions may be present in the reaction mixture and may be removed subsequently. The polymerization may be effected according to a batch process in which the ethylene is continuously or intermittently admitted to maintain the pressure in the vessel containing the maleic anhydride until the latter is all used up. The reaction components may be dissolved in benzene, toluene, xylene, n-hexane, mixed hexanes, octane or ethylene dichloride or mixtures thereof. The catalyst may be benzoyl peroxide, lauroyl peroxide, 2,4-dichloro-benzoyl peroxide, tertiary butyl peroxide, tertiary butyl hydroperoxide, diacetyl peroxide, diethyl peroxy-carbonate, dimethyl phenylhydroperoxy-methane, hydrogen peroxide, potassium persulphate, a ,a 1-azo diisobutyro-nitrile, azomethane and diazoamino benzene. The polymer is used in aqueous solution which may also contain glycerine, ethylene glycol, sorbitol, propylene glycol, a polyethylene glycol, polyglycerol or polypropylene oxide; a sulphonated animal, mineral or vegetable oil or mixture thereof; an emulsion of such sulphonated oils with animal, mineral or vegetable oils or Twitchell oil; an alkylbenzene sodium sulphonate in which the alkyl group contains from 10 to 20 carbon atoms, an alkali metal or ammonium mono-alkyl sulphosuccinate in which the alkyl group contains from 10 to 20 carbon atoms or a surface-active condensation product of ethylene oxide with an alkylated phenol having from 8 to 20 carbon atoms in the alkyl group or alkyl mercaptan having from 8 to 20 carbon atoms. Specifications 461,236 and 461,237, [both in Group IV], are referred to.ALSO:Nylon yarns are sized with an aqueous solution of an interpolymer of ethylene and maleic anhydride which has been converted to the free acid form or to an acid ester, and which, in the free acid form, has a specific viscosity of at least 0.1 when determined in a 1 per cent by weight solution in dimethyl formamide at 25 DEG C. The acid ester may be obtained by reacting the polymer with methanol, ethanol, iso-propanol, n-propanol, n-butanol, sec.-butanol, tert.-butanol, isobutanol, the various amyl alcohols, chloro- or nitro-substituted or unsaturated alcohols, alcohols having from 8 to 20 carbon atoms per molecule or ether-alcohols produced from ethylene oxide and low M.W. aliphatic alcohols, e.g. the compound <FORM:0815830/IV (c)/1> where n is from 2 to 10. Alternatively, the water-soluble interpolymer may be produced by interpolymerizing ethylene with a maleic acid half ester or mixture thereof with maleic anhydride. The size may also contain glycerine, ethylene glycol, sorbitol, propylene glycol, a polyethylene glycol, polyglycerol or polypropylene oxide; a sulphonated animal, mineral or vegetable oil or mixture thereof; an emulsion of such sulphonated oils with animal, mineral or vegetable oils or Twitchell oil; an alkylbenzene sodium sulphonate in which the alkyl group contains from 10 to 20 carbon atoms, an alkali metal or ammonium mono-alkyl sulpho-succinate in which the alkyl group contains from 10 to 20 carbon atoms or a surface-active condensation product of ethylene oxide with an alkylated phenol having from 8 to 20 carbon atoms in the alkyl group or alkyl mercaptan having from 8 to 20 carbon atoms. The sized yarns may be air-dried at 65 DEG to 85 DEG F. or oven-dried at 140 DEG to 250 DEG F. The sized yarn may be after-waxed. Specifications 461,236 and 461,237, [both in Group IV], are referred to.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US53273955A | 1955-09-06 | 1955-09-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB815830A true GB815830A (en) | 1959-07-01 |
Family
ID=22165071
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB27140/56A Expired GB815830A (en) | 1955-09-06 | 1956-09-05 | Sizing nylon yarns |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US2854357A (en) |
| DE (2) | DE1016228B (en) |
| FR (2) | FR1171287A (en) |
| GB (1) | GB815830A (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL124073C (en) * | 1961-06-21 | 1900-01-01 | ||
| BE621846A (en) * | 1961-08-31 | 1900-01-01 | ||
| NL283588A (en) * | 1961-10-06 | 1900-01-01 | ||
| US3228791A (en) * | 1962-10-26 | 1966-01-11 | Nat Starch Chem Corp | Sized polyolefin yarn |
| GB1093794A (en) * | 1964-04-14 | 1967-12-06 | Montedison Spa | Bonding elastomeric copolymers on to articles |
| US4397995A (en) * | 1980-12-29 | 1983-08-09 | Monsanto Company | Polymeric anti-tumor agent and method of preparation |
| US4461804A (en) * | 1981-05-29 | 1984-07-24 | Ppg Industries, Inc. | Aqueous sizing composition for glass fibers for use in producing a mat |
| US20260028435A1 (en) * | 2023-05-29 | 2026-01-29 | Jiangsu Yangnong Chemical Group Co., Ltd. | Method of Synthesizing Olefin Functional Polymer in Continuous Feeding Manner and Use of the Olefin Functional Polymer |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE623404C (en) * | 1930-05-26 | |||
| US2289222A (en) * | 1941-02-14 | 1942-07-07 | Du Pont | Yarn preparation |
| US2378629A (en) * | 1941-09-10 | 1945-06-19 | Du Pont | Copolymers of maleic anhydride |
| US2609350A (en) * | 1946-12-21 | 1952-09-02 | Gen Aniline & Film Corp | Textile finishing agent |
| US2651587A (en) * | 1947-06-02 | 1953-09-08 | Monsanto Chemicals | Treatment of textile materials |
| US2576915A (en) * | 1948-04-29 | 1951-12-04 | Monsanto Chemicals | Method of sizing yarns and composition therefor |
| US2616867A (en) * | 1950-08-30 | 1952-11-04 | Monsanto Chemicals | Composition for and method of sizing yarns |
| US2686137A (en) * | 1951-11-26 | 1954-08-10 | Monsanto Chemicals | Sized yarn and process of sizing |
-
1956
- 1956-09-05 DE DEM31630A patent/DE1016228B/en active Pending
- 1956-09-05 FR FR1171287D patent/FR1171287A/en not_active Expired
- 1956-09-05 GB GB27140/56A patent/GB815830A/en not_active Expired
- 1956-10-05 US US614061A patent/US2854357A/en not_active Expired - Lifetime
-
1957
- 1957-10-04 DE DEM35507A patent/DE1110131B/en active Pending
- 1957-10-04 FR FR748781A patent/FR73361E/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR1171287A (en) | 1959-01-23 |
| DE1110131B (en) | 1961-07-06 |
| DE1016228B (en) | 1957-09-26 |
| FR73361E (en) | 1960-06-27 |
| US2854357A (en) | 1958-09-30 |
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