GB500515A - A process for manufacturing films, ribbons, foils, threads and fibres - Google Patents

A process for manufacturing films, ribbons, foils, threads and fibres

Info

Publication number
GB500515A
GB500515A GB13675/38A GB1367538A GB500515A GB 500515 A GB500515 A GB 500515A GB 13675/38 A GB13675/38 A GB 13675/38A GB 1367538 A GB1367538 A GB 1367538A GB 500515 A GB500515 A GB 500515A
Authority
GB
United Kingdom
Prior art keywords
threads
liquid
sulphur
butadiene
coagulating
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
GB13675/38A
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.)
Bataafsche Petroleum Maatschappij NV
Original Assignee
Bataafsche Petroleum Maatschappij NV
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 Bataafsche Petroleum Maatschappij NV filed Critical Bataafsche Petroleum Maatschappij NV
Publication of GB500515A publication Critical patent/GB500515A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29DPRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
    • B29D99/00Subject matter not provided for in other groups of this subclass
    • B29D99/0078Producing filamentary materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2021/00Use of unspecified rubbers as moulding material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29LINDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2031/00Other particular articles
    • B29L2031/731Filamentary material, i.e. comprised of a single element, e.g. filaments, strands, threads, fibres

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Artificial Filaments (AREA)

Abstract

500,515. Artificial rubber threads and sheets. NAAMLOOZE VENNOOTSCHAP DE BATAAFSCHE PETROLEUM MAATSCHAPPIJ. May 7, 1938, Nos. 13675, 13676, 13677, 13678, 13679, and 13680. Convention dates, May 8, 1937, May 8, 1937, July 3, 1937, Dec. 22, 1937, April 7, 1938, and April 7, 1938. [Class 70] [Also in Group IV] Threads, fibres, foils, ribbons, and films, are obtained by extruding a solution of a polymerization product of butadiene into a congulation bath consisting of a liquid which does not dissolve the polymerization product but which is preferably readily miscible with the solvent used. The threads or other articles obtained may subsequently be hardened further by a thermal treatment. As solvent for the butadiene polymer there may be used benzene or other aromatic hydrocarbon, or piperylene, cyclohexene, cyclohexane, chloroform, carbon tetrachloride, other chlorinated saturated or unsaturated hydrocarbons, diethyl ether, dioxane, morpholine, ethyl acetate, vinyl acetate, quinoline, or carbon disulphide. The coagulating agent may be methyl, ethyl, or benzyl alcohol, acetone, acetophenone, benzaldehyde, butyraldehyde, water, aniline, triethanolamines, acetic acid, nitrobenzene, phenyl hydrazine, methyl aniline, diethylamine, phenylene diamines, or benzene sulphonic acid. The coagulating liquid may contain additions such as glycerol, soaps, salts, acids or bases. The temperature of the bath may be lower or higher than room temperature. The threads after leaving the first coagulation bath may be passed through another liquid which is miscible with the residual solvent. Coagulation may be carried out at elevated pressure. Spinning may be effected in a V-shaped tube containing the coagulating liquid. The threads may be stretched during the spinning operation. Stickiness may be avoided by passing the threads through a hot liquid, if desired at raised pressure. Hexyl, heptyl, or octyl alcohols, glycols, glycerol, ketones, or esters, may be -used for the hot liquid treatment. Stickiness may also be avoided by using a coagulating bath at a temperature above 100‹ C., or by coating the threads with a substance which reduces the surface tension and preferably has a hydrophobic character, e.g. sulphur in colloidal form, or colloidal sulphides. The threads still containing coagulating liquid may be contacted with a sulphur compound which is decomposed by the coagulation liquid with separation of sulphur. Sulphur chloride may be used, and it may if desired be added to the spinning solution. Substances may be added to the spinning solution or the coagulating bath which react with each other and precipitate sulphur or sulphides in the threads. Instead of sulphur, selenium may be deposited. Hydrogen sulphide may be caused to react with selenous acid so as to form colloidal sulphur and selenium. Stickiness may also be removed by coating the threads with a thin layer of talc, or clay. If the threads are passed through a bath of sulphur chloride under little or no tension, a strong and permanent crimping is obtained. The threads may be subjected to a thermal hardening treatment whereby the tensile strength is increased and the extensibility reduced. Hardening is preferably carried out at a temperature of 120-150‹ C. in the presence of a volatile halogen compound as catalyst, e.g. chlor-benzene, a halogen compound of toluene or xylene, ethyl chloride, ethyl bromide, propyl chloride, cyclohexyl chloride, or halogen ethers. The pressure may be at or below or above atmospheric. The butadiene polymer may be obtained from butadiene itself or from a mixture of butadiene and other diene hydrocarbons, or with polymers of a different character. Co-polymers of butadiene with vinyl compounds may be used. Dyes, plasticizers, fillers, and fire-proofing substances may be added to the spinning solution. In an example, a polymer of butadiene, obtained at room temperature in the presence of sodium as catalyst, is dissolved in benzene and the solution is extruded into methyl or ethyl alcohol. The thread obtained is wound on to a drum which dips into alcohol. The thread is then hardened by heating it in an atmosphere of carbon dioxide containing mono-chlorbenzene. In another example, a solution of butadiene polymer in dioxane is spun into a spinning funnel, the lower part of which passes into a narrow tube dipping into a tank of water. Liquid from the tank is pumped into the top of the funnel so as to maintain a constant level. The funnel is provided with an internal tube which surrounds the spinning nozzle and secludes it from the main stream of coagulating liquid. A small amount of fresh coagulating liquid may be introduced into the inner tube. The thread formed is stretched by the flowing liquid.
GB13675/38A 1937-05-08 1938-05-07 A process for manufacturing films, ribbons, foils, threads and fibres Expired GB500515A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
NL500515X 1937-05-08
NL837392X 1937-05-08

Publications (1)

Publication Number Publication Date
GB500515A true GB500515A (en) 1939-02-10

Family

ID=26643691

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13675/38A Expired GB500515A (en) 1937-05-08 1938-05-07 A process for manufacturing films, ribbons, foils, threads and fibres

Country Status (2)

Country Link
FR (1) FR837392A (en)
GB (1) GB500515A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2426719A (en) * 1943-07-28 1947-09-02 Du Pont Wet spinning of acrylonitrile polymers
DE903261C (en) * 1951-10-18 1954-02-04 Basf Ag Process for the production of artificial structures from solutions of organic, thread-forming substances in water-soluble, organic solvents
DE945720C (en) * 1951-11-29 1956-07-12 Rottweiler Kunstseidefabrik Ag Process for dissolving or gelatinizing polyacrylonitrile

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2426719A (en) * 1943-07-28 1947-09-02 Du Pont Wet spinning of acrylonitrile polymers
DE903261C (en) * 1951-10-18 1954-02-04 Basf Ag Process for the production of artificial structures from solutions of organic, thread-forming substances in water-soluble, organic solvents
DE945720C (en) * 1951-11-29 1956-07-12 Rottweiler Kunstseidefabrik Ag Process for dissolving or gelatinizing polyacrylonitrile

Also Published As

Publication number Publication date
FR837392A (en) 1939-02-08

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