US3511591A - Process and product of rendering cellulosic fabrics amenable to molding operations - Google Patents

Process and product of rendering cellulosic fabrics amenable to molding operations Download PDF

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Publication number
US3511591A
US3511591A US447098A US3511591DA US3511591A US 3511591 A US3511591 A US 3511591A US 447098 A US447098 A US 447098A US 3511591D A US3511591D A US 3511591DA US 3511591 A US3511591 A US 3511591A
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United States
Prior art keywords
fabric
liquid ammonia
cellulosic
bath
minutes
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US447098A
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English (en)
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Lester S Webb
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Deering Milliken Research Corp
Milliken Research Corp
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Milliken Research Corp
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    • 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
    • D06M11/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/58Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with nitrogen or compounds thereof, e.g. with nitrides
    • D06M11/59Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with nitrogen or compounds thereof, e.g. with nitrides with ammonia; with complexes of organic amines with inorganic substances
    • D06M11/61Liquid ammonia
    • 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
    • D06M2101/00Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/02Natural fibres, other than mineral fibres
    • D06M2101/04Vegetal fibres
    • D06M2101/06Vegetal fibres cellulosic

Definitions

  • This invention relates to presensitized cellulosic materials and more specifically to cellulosic materials which are rendered amendable to molding operations.
  • Cellulosic materials such as, for instance, paper, regenerated cellulosic films, and knitted and woven textile products composed wholly or partially of cellulosic fibers have been employed in operations which require the cellulosic materials to undergo a considerable degree of deformation.
  • the deforming operations are operations such as, for instance, laminating, packaging, and molding and the like.
  • cellulosic materials have a certain degree of flexibility, it is found that for certain applications the cellulosic materials have insuflicient strength and flexibility to undergo that degree of deformation which is a prerequisite to the utilization of cellulosic materials.
  • Laminates of cellulosic textile materials and vinyl films are to be preferred, for instance, over laminates of thermoplastic textile materials and vinyl films due to the fact that the fabric texture of a cellulosic material does not strike through the vinyl film and the cellulosic material has a high degree of adhesion to the vinyl film.
  • the inability of the cellulosic textile materials which have been heretofore known, however, to undergo deformations to which the laminates are subsequently subjected, has severely limited the use of cellulosic textile materials.
  • liquid ammonia is preferably maintained at a temperature of from about 60 C. to below about 32 C., the exposure time being for an interval of from about one second to about five minutes.
  • the liquid ammonia immersion operation is preferably followed by a 3,511,591 Patented May 12, 1970 drying operation wherein exposure to moisture is minimized.
  • the cellulosic material should be a cellulosic material which has been subjected to stresses in its manufacture.
  • a stressed cellulosic material may be considered as a material which when not subjected to external mechanical forces is capable of being reduced to a more relaxed state.
  • Materials which meet the definition of a stressed cellulosic material are drawn sheets and filaments of cellulosic materials, knitted and woven textile materials, tension calendered paper and the like.
  • the stressed cellulosic material should contain in excess of alpha cellulose.
  • the treatment converts substantial portions of the cellulosic molecule from a crystalline configuration to an amorphous configuration, the change being readily apparent from a viewing of the X-ray diffractogram before and after liquid ammonia treatment.
  • the amorphous structure of the cellulose molecule has been found to be more amenable to conforming to a tortuous configuration than the crystalline structure.
  • the amorphous structure is also a structure which may be readily reconverted to the initial crystalline structure.
  • a reversion of the cellulosic material from an amorphous structure to a crystalline structure results in the permanent setting of a cellulosic material to that tortuous configuration to which it has conformed itself while in the amorphous state.
  • the liquid ammonia treatments also result in a shrinkage of the cellulosic material and a substantial increase in strength.
  • the cellulosic material of this invention may be maintained in an amorphous structure for substantial periods of time at temperatures of 25 C. or less, it is preferred to increase the stability of the amorphous structure by impregnation with a bond inhibitor.
  • these bond inhibitors fall into two groups which are liquid ammonia compatable polymers and liquid ammonia compatable plasticizers.
  • the bond inhibitor may be employed by simply dissolving the inhibitor in the liquid ammonia treating bath.
  • Inhibitors which are effective in accordance with this invention are compounds capable of interfering with or substantially preventing the formation of hydrogen bonds between adjacent molecular chains of cellulose.
  • the polyhydric alcohols containing 2 to 6 carbon atoms or mixtures thereof have been found to be especially effective and preferably use is made of dihydric and trihydric alcohols exemplified by ethylene glycol, propylene glycol, glycerine, diethanolamine, triethanolamine, trimethylene glycol, butane dioles such as tetramethylene glycol, butane triol, pentane triol, diethylene glycol, dipropylene glycol and triethylene' glycol.
  • Polymeric materials which are suitable for use as inhibitors are any of the polymeric materials which are soluble in liquid ammonia as Well as any of the polymeric materials which are soluble in an organic solvent which is soluble in liquid ammonia.
  • the term polymeric material as employed herein includes monomeric materials which may be cured in situ to a polymer.
  • Polymeric materials which have been found to be especially suitable for purposes of this invention are phenol formaldehyde, melamine formaldehyde, urea formaldehyde, dimethylol ethyleneurea, dihydroxy dimethylol ethyleneurea, polyvinyl alcohol, polyethylene glycol, polyacrylic acid, polyvinl acetate, the sodium salt of styrene-maleic anhydride copolymer and end blocked isocyanate containing polymers.
  • the inhibitor is effective over a range of proportions extending from about 5 O to 150 parts by weight, preferably about per 100 parts by weight of cellulose.
  • EXAMPLE I A high stretch all cotton knit fabric having a weight of 4.55 yards per pound knitted from singles twenty yarn on an eighteen inch diameter Camber machine so as to have 26 plus or minus 2 wales per inch and 24 plus or minus 2 courses per inch is immersed in a liquid ammonia bath.
  • the liquid ammonia bath is maintained at approximately 33 C. and the fabric is subjected to an immersian time in this bath for about 2 minutes.
  • the treated fabric is then removed from the bath and passed through a Fleissner drier at the rate of about 1 yard per minute, the rate subjecting the fabric to a total drying time of from about 4 /2 minutes to about minutes.
  • the improvement obtained by the liquid ammonia treatment was determined by evaluating an untreated section of the previously identified fabric by means of a Scott Grab Tensile test and then evaluating a treated section in swollen state (area shrinkage-25%) of the previously identified fabric by means of the same test. The results being as follows:
  • EXAMPLE III A high stretch jersey knit all rayon fabric having a weight of 4.05 ounces per square yard prepared from singles fifteen viscose rayon staple fiber yarn in a manner so as to have 16.4 wales per inch and 19.2 courses per inch is subjected to a liquid ammonia bath.
  • the liquid ammonia bath is maintained at a temperature of about 33 C., the fabric being immersed in the bath for about 2 minutes.
  • the fabric is then removed and passed through a Fleissner drier at the rate of about 1 yard per minute, the rate being such to subject the fabric to drying conditions for from about 4 /2 minutes to about 5 minutes.
  • the improvement obtained in treating the fabric with liquid ammonia is determined by testing an untreated sample of the previously identified fabric by means of a Scott Grab Tensile test and then repeating the test on a sample of the previously identified fabric which has undergone liquid ammonia treatment, the results being as follows:
  • a single jersey stitch paper fabric yarn prepared from paper yarn produced by slitting 10 pound per ream kraft paper to inch width and folding and crimping is subjected to the action of a liquid ammonia bath.
  • the paper fabric prior to the liquid ammonia bath treatment is found to have 6 courses per inch and about 4 wales per inch.
  • the liquid ammonia bath is maintained at a temperature of about 33 C., the fabric being immersed in a liquid ammonia bath for a period of about 2 minutes.
  • the fabric is then removed and passed through a Fleissner drier at a rate of about 1 yard per minute, the rate being suflicient to subject the paper fabric to a drying time for a period of from about 4 /2 minutes to about 5 minutes.
  • a sample section of the previously described paper fabric is then subjected to a Scott Grab Tensile test, the test being repeated on a sample section of the previously described paper fabric which has undergone liquid ammonia treatment.
  • a comparison of the test results of the Scott Grab Tensile test is found to show an improvement in percent elongation of the liquid ammonia treated fabric over the paper fabric which has not undergone liquid ammonia treatment.
  • EXAMPLE V A cotton print cloth having ends and 80 picks per inch prepared from singles forty yarn having a weight for a 39 inch width of 4 yards per pound is subjected to the action of a liquid ammonia bath, the liquid ammonia bath having glycerine dissolved therein in quantities of about 5% by Weight.
  • the liquid ammonia bath is maintained at a temperature of about -33 (3., the fabric being immersed in the liquid ammonia bath for a period of about 2 minutes.
  • the fabric is then removed and passed through a. Fleissner drier at a rate of about 1 yard per minute, the rate being sufficient to the subject the fabric Scott Grab Tensile Breaking Str. (lbs.)
  • EXAMPLE VI A 1 inch by 6 inch sample of untreated regenerated cellulose film having a thickness of .001 inch is immersed in a liquid ammonia bath containing 5% by weight diethylene glycol. The liquid ammonia bath is maintained at approximately 33 C. and the regenerated cellulose film is subjected to an immersion time of about 2 minutes. The ammonia treated film is then removed and allowed to dry at room temperatures under substantially moisture free conditions. The improvement obtained by the liquid ammonia treatment of film was determined by evaluating an untreated 1 inch by 3 inch sample of the previously identified film by placing the lengthwise end of the film in the jaws of an Instron machine. The test was then repeated by placing the ends of the short axis of the sample in the jaws of the Instron machine. Comparable tests were then run on the treated regenerated cellulose film sample with the overall result being as follows:
  • a cotton broadcloth of 136 x 64 construction prepared from single thirties fill yarns and single forties warp yarns is subjected to the action of a liquid ammonia bath, the liquid ammonia bath containing 5% based on the weight of the ammonia of dihydroxy dimethyl ethyleneurea.
  • the fabric is maintained in the bath for 4 minutes and then removed and immediately molded on a brassiere cup molding device, the mold being maintained at a temperature of 253 F.
  • the molded fabric was found to retain its dimensional stability and to be durable to washmg.
  • EXAMPLE VIII An all rayon challis fabric of 68 x 62 construction prepared from single thirties rayon staple yarn in both warp and fill directions is immersed for 4 minutes in a liquid ammonia treating bath containing 5% by weight based on the weight of the liquid ammonia of urea formaldehyde. The fabric is then removed and passed through a Fleissner drier at the rate of about 1 yard per minute, the rate being sufiicient to subject the fabric to a drying time for a period of from about 4 /2 minutes to about 5 minutes. The dried fabric is then placed in a brassiere cup mold, the mold being maintained at a temperature of about 253 F. The molded product is found to retain its dimensional stability and to be durable to washing.
  • the Scott Grab Tensile test which has been called for in the previous examples is a standard method of tests 6 for breaking load and elongation of textile fabrics and is set forth in ASTM designation D1682-64.
  • the Grab test is a test in which only part of the width of the specimen is gripped in the clamps of the testing equipment. For example, in the specimen which is 4 inches and the width of the gripping device 1 inch, the
  • the Grab method is applicable whenever it is desired to determine the effective strength of the fabric in use, that is the strength of the yarn in specific width together with the additional strength contributed by adjacent yarn.
  • the cellulosic materials of this invention lend themselves to molding operations and especially to the molding operations wherein the cellulosic material retains its dimensional stability by itself or as part of a laminate such as, for instance, a cellulosic fabric-vinyl film laminate. Where the cellulosic material is to retain its molded configuration without undergoing laminating operations, it is preferred that the cellulosic material be treated with a liquid ammonia bath containing a thermosetting resin.
  • the molding operations may be any of the molding operations well known to the art such as vacuum molding operations and pressure moldmg operations.
  • a process for rendering a stressed woven or knit cellulosic fabric amenable to molding operations which comprises immersing said fabric while in a relaxed state in a bath consisting essentially of a thermosetting resin and liquid ammonia maintained at a temperature from about 60 C. to about 30 C. for a period from about A minute to about 4 minutes and drying the ammonia treated fabric under conditions of minimal moisture exposure.
  • a stress relieved woven or knit cellulosic fabric prepared according to the process of claim 1.
  • a stress relieved woven or knit cellulosic fabric prepared according to the process of claim 3.

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Artificial Filaments (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
US447098A 1965-04-09 1965-04-09 Process and product of rendering cellulosic fabrics amenable to molding operations Expired - Lifetime US3511591A (en)

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Application Number Priority Date Filing Date Title
US44709865A 1965-04-09 1965-04-09

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US3511591A true US3511591A (en) 1970-05-12

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US (1) US3511591A (en, 2012)
BE (1) BE679303A (en, 2012)
CH (1) CH474602A (en, 2012)
DE (1) DE1594989A1 (en, 2012)
ES (1) ES325235A1 (en, 2012)
GB (1) GB1141016A (en, 2012)
LU (1) LU50857A1 (en, 2012)
NL (1) NL6604641A (en, 2012)
SE (1) SE335846B (en, 2012)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3905763A (en) * 1972-03-14 1975-09-16 Omnium De Prospective Ind Sa Processes for treating polyamides
US4425131A (en) 1979-03-05 1984-01-10 Cluett, Peabody & Co., Inc. Method of improved pile appearance in liquid ammonia treated fabric; pretreatment with crease resistant resin
US4475917A (en) * 1981-09-24 1984-10-09 Asahi Kasei Kogyo Kabushiki Kaisha Process for modifying regenerated cellulose fiber
US5910279A (en) * 1996-04-12 1999-06-08 Nisshinbo Industries, Inc. Method for forming durable creases in cellulosic fiber textile

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2824420B2 (de) * 1978-06-03 1981-05-07 Ivanovskij naučno-issledovatel'skij institut chlopčatobumažnoj promyšlennosti, Ivanovo Verfahren zur Mercerisierung von Baumwollgarn
DE4312219C2 (de) * 1993-04-14 2002-05-08 Thueringisches Inst Textil Verfahren zur Reduzierung der Fibrillierbarkeit von lösungsgesponnenen Cellulosefasern
JP3743790B2 (ja) * 1995-08-18 2006-02-08 シキボウ株式会社 改質されたセルロース繊維、その製造方法及び繊維製品
DE19639141C1 (de) * 1996-09-24 1998-03-05 Hans Celler Verfahren zur Behandlung von Textilgut mit flüssigem Ammoniak sowie Vorrichtung zur Durchführung dieses Verfahrens
DE19742692A1 (de) * 1997-09-26 1999-04-01 Rhodia Acetow Ag Verfahren zur Aktivierung von Polysacchariden

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE630310A (en, 2012) * 1962-04-03
US1989098A (en) * 1925-06-20 1935-01-29 Lilienfeld Leon Manufacture of artificial threads
US1998551A (en) * 1931-04-01 1935-04-23 Ig Farbenindustrie Ag Mercerizing process
US2211872A (en) * 1937-09-09 1940-08-20 Celanese Corp Treatment of textile materials
US2462927A (en) * 1943-11-06 1949-03-01 Du Pont Artificial filaments and yarn
US2528793A (en) * 1946-01-26 1950-11-07 Kendall & Co Cotton felt and method of making the same
GB841401A (en) * 1957-01-29 1960-07-13 Spinnfaser Ag A process for improving the utility and crimping intensity of regenerated cellulose textile fibres
US2955014A (en) * 1955-03-04 1960-10-04 Segal Leon Process of treating native cellulose with a liquid alkylenepolyamine and a textile resin
US3005728A (en) * 1956-10-19 1961-10-24 Tee Pak Inc Cellulosic laminates
US3145132A (en) * 1961-08-02 1964-08-18 Kendall & Co Woven stretchable fabrics
US3347963A (en) * 1964-12-28 1967-10-17 Little Inc A Method of stretch forming rayons

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1989098A (en) * 1925-06-20 1935-01-29 Lilienfeld Leon Manufacture of artificial threads
US1998551A (en) * 1931-04-01 1935-04-23 Ig Farbenindustrie Ag Mercerizing process
US2211872A (en) * 1937-09-09 1940-08-20 Celanese Corp Treatment of textile materials
US2462927A (en) * 1943-11-06 1949-03-01 Du Pont Artificial filaments and yarn
US2528793A (en) * 1946-01-26 1950-11-07 Kendall & Co Cotton felt and method of making the same
US2955014A (en) * 1955-03-04 1960-10-04 Segal Leon Process of treating native cellulose with a liquid alkylenepolyamine and a textile resin
US3005728A (en) * 1956-10-19 1961-10-24 Tee Pak Inc Cellulosic laminates
GB841401A (en) * 1957-01-29 1960-07-13 Spinnfaser Ag A process for improving the utility and crimping intensity of regenerated cellulose textile fibres
US3145132A (en) * 1961-08-02 1964-08-18 Kendall & Co Woven stretchable fabrics
BE630310A (en, 2012) * 1962-04-03
US3347963A (en) * 1964-12-28 1967-10-17 Little Inc A Method of stretch forming rayons

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3905763A (en) * 1972-03-14 1975-09-16 Omnium De Prospective Ind Sa Processes for treating polyamides
US4425131A (en) 1979-03-05 1984-01-10 Cluett, Peabody & Co., Inc. Method of improved pile appearance in liquid ammonia treated fabric; pretreatment with crease resistant resin
US4475917A (en) * 1981-09-24 1984-10-09 Asahi Kasei Kogyo Kabushiki Kaisha Process for modifying regenerated cellulose fiber
US5910279A (en) * 1996-04-12 1999-06-08 Nisshinbo Industries, Inc. Method for forming durable creases in cellulosic fiber textile

Also Published As

Publication number Publication date
CH474602A (fr) 1969-03-14
LU50857A1 (en, 2012) 1966-06-07
DE1594989A1 (de) 1971-05-27
SE335846B (en, 2012) 1971-06-14
ES325235A1 (es) 1967-01-01
GB1141016A (en) 1969-01-22
NL6604641A (en, 2012) 1966-10-10
BE679303A (en, 2012) 1966-09-16

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