US3315329A - Process for the manufacture of chemical lace - Google Patents

Process for the manufacture of chemical lace Download PDF

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Publication number
US3315329A
US3315329A US404483A US40448364A US3315329A US 3315329 A US3315329 A US 3315329A US 404483 A US404483 A US 404483A US 40448364 A US40448364 A US 40448364A US 3315329 A US3315329 A US 3315329A
Authority
US
United States
Prior art keywords
cellulose
base cloth
water
alkali
acrylonitrile
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 - Lifetime
Application number
US404483A
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English (en)
Inventor
Yoshioka Yoshihide
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.)
Kurashiki Rayon Co Ltd
Original Assignee
Kurashiki Rayon Co Ltd
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 Kurashiki Rayon Co Ltd filed Critical Kurashiki Rayon Co Ltd
Application granted granted Critical
Publication of US3315329A publication Critical patent/US3315329A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06QDECORATING TEXTILES
    • D06Q1/00Decorating textiles
    • D06Q1/02Producing patterns by locally destroying or modifying the fibres of a web by chemical actions, e.g. making translucent
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B13/00Preparation of cellulose ether-esters
    • C08B13/02Cellulose ether xanthates
    • 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
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04CBRAIDING OR MANUFACTURE OF LACE, INCLUDING BOBBIN-NET OR CARBONISED LACE; BRAIDING MACHINES; BRAID; LACE
    • D04C1/00Braid or lace, e.g. pillow-lace; Processes for the manufacture thereof
    • D04C1/02Braid or lace, e.g. pillow-lace; Processes for the manufacture thereof made from particular materials
    • D04C1/04Carbonised or like lace
    • DTEXTILES; PAPER
    • D05SEWING; EMBROIDERING; TUFTING
    • D05CEMBROIDERING; TUFTING
    • D05C17/00Embroidered or tufted products; Base fabrics specially adapted for embroidered work; Inserts for producing surface irregularities in embroidered products
    • 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S8/00Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
    • Y10S8/13Cyanoethylation of fibers

Definitions

  • a general process for manufacturing chemical lace includes embroidering a base cloth which dissolves in a certain solvent, preferably in water or diluted alkali solution, with a fiber which does not dissolve in said solvent and thereafter dissolving the base cloth with said solvent.
  • a base cloth of fiber for chemical lace has been prepared hitherto as follows:
  • the object of the invention is to provide a process for manufacturing chemical lace by using a base cloth prepared by a new method.
  • an excellent base cloth for chemical lace may be manufactured by a method comprising dissolving the reaction product which is obtained by reacting alkali cellulose simultaneously with carbon disulfide and acrylonitrile in diluted alkali solution to form viscose, spinning said viscose into fiber, and fabricating woven or non-woven fabric containing said fiber.
  • a chemical lace may be manufactured by embroidering the base cloth obtained in the manner described above with a diluted alkalior water-insoluble fiber, winding the resulting cloth on a frame, dipping it in a diluted alkali solution or water and, while Winding the cloth on the frame, moving the liquid, and dissolving off the base cloth.
  • alkali cellulose contains no compound which wastes acrylonitrile such as Na S and Na CS 98 100% of the acrylonitrile may be utilized advantageously for the reaction with the cellulose, the utilization ratio of acrylonitrile being very high.
  • the rate of said reaction is the highest.
  • the degration of alkali cellulose is restricted by simultaneously reacting carbon disulfide and acrylonitrile with said alkali cellulose as compared to carbon disulfide alone in xanthation.
  • the amount of carbon disulfide is more than 10%. Since carbon disulfide and acrylonitrile are reacted with alkali cellulose simultaneously, the xanthogenation and cyanoethylation of the cellulose occur at the same time, both of the reactions serving to make the cellulose soluble, so the carbon disulfide in such a small amount as 10% based on the weight of cellulose has a sufficient effect. With an amount of carbon disulfide less than 10%, a fiber for base cloth desired for the object of the invention can not be obtained even by increasing the amount of acrylonitrile. The optimum amount of carbon disulfide is 20-50%.
  • the amount of acrylonitrile is more than 20% based on the weight of cellulose.
  • An amount less than 20% is unsuitable for the invention, because the fiber prepared under such conditions swells and does not dissolve in diluted alkali solution.
  • the amount of acrylonitrile used in the process for cyanoethylating alkali cellulose must be more than 20% based on the weight of cellulose, more preferably more than 30%.
  • the amount of acrylonitrile is preferably rnore than 60%, more preferably and more than may be added.
  • a woven fabric consisting alone or mainly of said diluted alkalior water-soluble cyanoethyl cellulose or dry or wet unwoven fabric thereof may be used.
  • a chemical lace in which the insoluble fiber remains as a net can be obtained by dissolving off the soluble fiber of the base cloth with diluted alkali solution or water.
  • a diluted alkali-insoluble fiber such as polyamide synthetic fiber may be used and when using water, not only polyvinyl alcohol synthetic fiber but also other all artificial and natural fibers having water resisting property may be used, although a water-soluble fiber such as alginate fiber, non-acetalized polyvinyl alcohol synthetic fiber etc. is unsuitable.
  • an aged alkali cellulose prepared according to the conventional method is added a mixture of carbon disulfide in an amount of more than 10 'by Weight based on the cellulose and acrylonitrile in an amount of more than 20% by weight based on the cellulose, and the mixture is reacted at 25 C. for 60-120 minutes. After the reaction is complete, the product is dissolved in diluted alkali solution to form a viscose containing 4-10% of cellulose and 38% of total alkali. The resulting viscose is spun in a spinning bath containing 5-15% of H 80 10-30% of Na SO and 0.55% of ZnSO to yield a rayon of -150 deniers.
  • the rayon yarn is neutralized with alkali in a concentrated Glaubers salt or alcohol, washed then with diluted alcohol to remove the salt and dried.
  • the yarn is woven to plain weave as base cloth.
  • the base cloth is embroidered with a diluted alkalior waterinsoluble fiber, after which the resulting cloth is wound on a frame, which is dipped in diluted alkali solution or water and the liquid is moved while winding the cloth on the frame to dissolve off the base cloth.
  • a chemical lace may be manufactured.
  • the hank When dissolving the cloth, the hank may be rotated or vibrated or travelled. In such a case, however, the base cloth should be moved together with the frame while it is wound on the frame. If the base cloth is moved indifferently from the frame, the embroidered part is damaged. However, if the dissolving liquid is moved and also the base cloth together with the frame is moved as one body, not only may this disadvantage be eliminated but also the time for dissolution may be decreased.
  • the frame to be used in the invention includes a frame consisting of polygonal prism structure, or a cylindrical frame consisting of a perforated wall etc. It is no matter that the base cloth is moved slightly by moving the liquid.
  • a vibration method in which steam is blown into the liquid bath a mechanical agitation method, a vibration method by ultra sonic waves, a movement method in which the liquid in the bath is circulated by a pump and the like, etc.
  • the diluted alkali solution in the invention means the solution at room temperature or heated solution having an alkali concentration of 1-5%, and water includes cold, warm and hot water and hot water under pressure. In particular, diluted alkali solution or water at room temperatures are most suitable for use.
  • Example 1 To an alkali cellulose obtained by the conventional method which is aged up to a degree of polymerization of 310 are added carbon disulfide in an amount of 40% by Weight based on the cellulose and acrylonitrile in an amount of 40% by weight based on the cellulose, and the mixture is reacted at 25 C. for 2 hours. The resulting product is dissolved in diluted alkali solution to yield a viscose containing 8.5% of cellulose and 5.5% of total alkali.
  • the viscose is spun in a spinning bath containing of H SO of Na SO and 2% of ZnSO to yield a rayon having single filaments and a total denier of 150.
  • the rayon yarn is neutralized with sodium carbonate in a saturated bath of Glaubers salt, washed then with diluted methanol and dried.
  • the resulting rayon yarn is woven into a plain weave which, as base cloth, is embroidered with a water resisting polyvinyl alcohol synthetic fiber.
  • the fabric embroidered on the base cloth is wound on a frame consisting of a polygonal prism structure, which is dipped in 3.5% caustic soda solution at room temperature to dissolve off the base cloth by stirring the liquid.
  • the fabric obtained is neutralized with diluted sulfuric acid solution, washed with water and dried to yield a chemical lace consisting of water resistant polyvinyl alcohol synthetic fiber.
  • Example 2 To an alkali cellulose obtained by the conventional method which is aged up to a degree of polymerization of 300 are mixed carbon disulfide in an amount of 40% by weight based on cellulose and acrylonitrile in an amount of 80% by weight based on the cellulose simultaneously and the mixture is reacted at 25 C. for 2.5 hours.
  • a base cloth of plain weave is woven in the same manner as described in Example 1.
  • a fabric embroidered with viscose rayon on the base cloth is wound on a frame which is dipped in water at about 50 C. to dissolve and remove oil the base cloth while circulating water by means of a pump.
  • chemical lace consisting of viscose rayon yarn may be obtained.
  • Example 3 To an alkali cellulose obtained by the conventional method which is aged up to a degree of polymerization of 300 are added carbon disulfide in an amount of 50% by weight based on the cellulose and acrylonitrile in an amount of by weight based on the cellulose simultaneously and the mixture is reacted at 25 C. for 2 hours. The product is dissolved in diluted alkali solution, and spun in a spinning bath having the same composition as in Example 1. The resulting fiber is neutralized, washed and then dried.
  • the resulting rayon yarn is woven into a base cloth which is embroidered with cotton yarn.
  • the fabric obtained is wound on a frame, which is dipped in water at ordinary temperature to dissolve off the base cloth (the dissolving liquid being circulated by means of a pump).
  • a chemical lace is obtained in which only the portion embroidered with cotton yarn remains.
  • a process for the manufacture of chemical lace which comprises reacting alkali cellulose simultaneously wth more than 10% by weight based on the cellulose of carbon disulfide and more than 20% by weight based on the cellulose of acrylonitrile, dissolving the resulting reaction product in dilute alkali solution to form a viscose, spinning fibers therefrom, manufacturing from said fibers a base cloth, embroidering the base cloth with a different fiber insoluble in a solvent selected from the group consisting of dilute alkali and water to form an embroidered fabric, and dipping the embroidered fabric in a solvent selected from the group consisting of dilute alkali and water to dissolve the base cloth.
  • a process for the manufacture of chemical lace which comprises dissolving a reaction product obtained by reacting alkali cellulose simultaneously with more than 10% by weight based on the cellulose of carbon disulfide and more than 20% by weight based on the cellulose of acrylonitrile to form a viscose, spinning the viscose into fibers, manufacturing from said fibers a base cloth, embroidering the base cloth with another fiber insoluble in a solvent selected from the group consisting of dilute alkali and water to form an embroidered fabric, and dipping the embroidered fabric in a solvent selected from the group consisting of dilute alkali and water to dissolve the 'base cloth.

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Textile Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Biochemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • Artificial Filaments (AREA)
US404483A 1963-10-21 1964-10-16 Process for the manufacture of chemical lace Expired - Lifetime US3315329A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5649863 1963-10-21

Publications (1)

Publication Number Publication Date
US3315329A true US3315329A (en) 1967-04-25

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Family Applications (1)

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Country Status (3)

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US (1) US3315329A (de)
CH (1) CH425426A (de)
DE (1) DE1519534A1 (de)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3377678A (en) * 1965-12-27 1968-04-16 Nihon Vinylon Co Ltd Half-soluble special fabric and a method of manufacturing embroidery lace thereon
US3521638A (en) * 1969-02-10 1970-07-28 Du Pont Fabrics having water soluble discrete areas and methods of making
US3658023A (en) * 1969-07-15 1972-04-25 Alfred G Rossi Fabric and method for making the fabric
US4570311A (en) * 1981-12-07 1986-02-18 Firma Carl Freudenberg Method for manufacturing water soluble fabric for chemical laces
US5111760A (en) * 1989-06-22 1992-05-12 Garzone Jr Raymond G Double-embroidered lace
EP0823502A3 (de) * 1996-08-08 1998-04-22 Madeira Asia Pte. Ltd. Maschinenstickverfahren

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB320528A (en) * 1928-10-18 1929-10-17 Eugen Baer Process for the production of a ground fabric for embroidery purposes
GB525038A (en) * 1938-02-14 1940-08-20 Wacker Chemie Gmbh Improvements in the manufacture of ornamental materials such as lace, embroidery andthe like
US2439865A (en) * 1944-03-01 1948-04-20 Celanese Corp Manufacture of water-soluble textile materials
US2499501A (en) * 1945-10-05 1950-03-07 American Viscose Corp Cellulose derivatives
GB636295A (en) * 1948-02-18 1950-04-26 Courtaulds Ltd Improvements in and relating to the production of water-soluble mixed cellulose ethers
US2724632A (en) * 1954-08-09 1955-11-22 Londat Aetz Fabric Co Cyanoethylated cellulose textiles modified with chromic and periodic acids and process of making same
US3052511A (en) * 1960-02-23 1962-09-04 Robert M Reinhardt Process for the production of alkalisoluble cellulosic textile materials by etherifying the cellulose with specific ether groups and oxidizing with nitrogen dioxide
US3097956A (en) * 1960-11-07 1963-07-16 American Cyanamid Co Cyanoethylated cellulose solutions

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB320528A (en) * 1928-10-18 1929-10-17 Eugen Baer Process for the production of a ground fabric for embroidery purposes
GB525038A (en) * 1938-02-14 1940-08-20 Wacker Chemie Gmbh Improvements in the manufacture of ornamental materials such as lace, embroidery andthe like
US2439865A (en) * 1944-03-01 1948-04-20 Celanese Corp Manufacture of water-soluble textile materials
US2499501A (en) * 1945-10-05 1950-03-07 American Viscose Corp Cellulose derivatives
GB636295A (en) * 1948-02-18 1950-04-26 Courtaulds Ltd Improvements in and relating to the production of water-soluble mixed cellulose ethers
US2724632A (en) * 1954-08-09 1955-11-22 Londat Aetz Fabric Co Cyanoethylated cellulose textiles modified with chromic and periodic acids and process of making same
US3052511A (en) * 1960-02-23 1962-09-04 Robert M Reinhardt Process for the production of alkalisoluble cellulosic textile materials by etherifying the cellulose with specific ether groups and oxidizing with nitrogen dioxide
US3097956A (en) * 1960-11-07 1963-07-16 American Cyanamid Co Cyanoethylated cellulose solutions

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3377678A (en) * 1965-12-27 1968-04-16 Nihon Vinylon Co Ltd Half-soluble special fabric and a method of manufacturing embroidery lace thereon
US3521638A (en) * 1969-02-10 1970-07-28 Du Pont Fabrics having water soluble discrete areas and methods of making
US3658023A (en) * 1969-07-15 1972-04-25 Alfred G Rossi Fabric and method for making the fabric
US4570311A (en) * 1981-12-07 1986-02-18 Firma Carl Freudenberg Method for manufacturing water soluble fabric for chemical laces
US5111760A (en) * 1989-06-22 1992-05-12 Garzone Jr Raymond G Double-embroidered lace
EP0823502A3 (de) * 1996-08-08 1998-04-22 Madeira Asia Pte. Ltd. Maschinenstickverfahren
CN1069938C (zh) * 1996-08-08 2001-08-22 马德拉亚洲有限公司 用于提供一种带有一凸出机织刺绣图案的物品的方法

Also Published As

Publication number Publication date
CH1361264A4 (de) 1966-08-15
CH425426A (de) 1967-05-31
DE1519534A1 (de) 1970-03-12

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