EP0808939A1 - Procédé pour rendre les textiles de tissus à base de cellulose non rétrécissable - Google Patents

Procédé pour rendre les textiles de tissus à base de cellulose non rétrécissable Download PDF

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Publication number
EP0808939A1
EP0808939A1 EP97108329A EP97108329A EP0808939A1 EP 0808939 A1 EP0808939 A1 EP 0808939A1 EP 97108329 A EP97108329 A EP 97108329A EP 97108329 A EP97108329 A EP 97108329A EP 0808939 A1 EP0808939 A1 EP 0808939A1
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EP
European Patent Office
Prior art keywords
treatment
fabric
hot water
caustic alkali
resin
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.)
Withdrawn
Application number
EP97108329A
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German (de)
English (en)
Inventor
Yuichi c/o Nisshinbo Ind. Inc. Miai Plant Yanai
Takayuki Nisshinbo Ind. Inc. Miai Plant Hirai
Masayoshi Nisshinbo Ind. Inc. Miai Plant Oba
Kiyoshi Nisshinbo Ind. Inc. Miai Plant Ikeda
Yasushi Nisshinbo Ind. Inc. Miai Plant Takagi
Takeo Nisshinbo Ind. Inc. Miai Plant Ishikawa
Kazuhiko Nisshinbo Ind. Inc. Miai Plant Harada
Hirotaka Nisshinbo Ind. Inc. Miai Plant Iida
Ryuichi Nisshinbo Ind. Inc. Miai Plant Ito
Osamu c/o Nisshinbo Ind. Inc. Hasegawa
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.)
Nisshinbo Holdings Inc
Original Assignee
Nisshinbo Industries Inc
Nisshin Spinning Co Ltd
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Filing date
Publication date
Priority claimed from JP26016996A external-priority patent/JP3073447B2/ja
Priority claimed from JP08260166A external-priority patent/JP3073446B2/ja
Priority claimed from JP26249096A external-priority patent/JP3154149B2/ja
Priority claimed from JP8298217A external-priority patent/JP3011112B2/ja
Application filed by Nisshinbo Industries Inc, Nisshin Spinning Co Ltd filed Critical Nisshinbo Industries Inc
Priority to EP02016577A priority Critical patent/EP1270797A2/fr
Publication of EP0808939A1 publication Critical patent/EP0808939A1/fr
Withdrawn legal-status Critical Current

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    • 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
    • D06M11/00—Treating 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
    • D06M11/58—Treating 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
    • D06M11/59—Treating 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
    • D06M11/61—Liquid ammonia
    • 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
    • D06M11/00—Treating 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
    • D06M11/01—Treating 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 hydrogen, water or heavy water; with hydrides of metals or complexes thereof; with boranes, diboranes, silanes, disilanes, phosphines, diphosphines, stibines, distibines, arsines, or diarsines or complexes thereof
    • 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
    • D06M11/00—Treating 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
    • D06M11/32—Treating 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 oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/36—Treating 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 oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/38—Oxides or hydroxides of elements of Groups 1 or 11 of the Periodic Table
    • 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
    • D06M11/00—Treating 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
    • D06M11/32—Treating 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 oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/36—Treating 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 oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/38—Oxides or hydroxides of elements of Groups 1 or 11 of the Periodic Table
    • D06M11/40—Oxides or hydroxides of elements of Groups 1 or 11 of the Periodic Table combined with, or in absence of, mechanical tension, e.g. slack mercerising
    • 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
    • D06M11/00—Treating 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
    • D06M11/84—Treating 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 combined with mechanical treatment
    • 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
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/11—Compounds containing epoxy groups or precursors thereof
    • 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
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/12—Aldehydes; Ketones
    • 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
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/12—Aldehydes; Ketones
    • D06M13/123—Polyaldehydes; Polyketones
    • 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
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/12—Aldehydes; Ketones
    • D06M13/127—Mono-aldehydes, e.g. formaldehyde; Monoketones
    • 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
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/184—Carboxylic acids; Anhydrides, halides or salts thereof
    • D06M13/192—Polycarboxylic acids; Anhydrides, halides or salts thereof
    • 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
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
    • D06M15/423—Amino-aldehyde resins
    • 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
    • D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/02—Natural fibres, other than mineral fibres
    • D06M2101/04—Vegetal fibres
    • D06M2101/06—Vegetal fibres cellulosic

Definitions

  • This invention relates to a method for the shrink-proof treatment of a cellulosic fiber textile. More particularly, it relates to a method for treating a cellulosic fiber textile to be fully shrink-proof without a substantial loss of strength so that it may experience minimal shrinkage after washing and minimal hand-and-feel hardening after repetitive washing.
  • cellulosic fiber textiles have been widely used as clothing materials since they have the advantages of moderate moisture absorption, good hand-and-feel textures, and ease of treatment. Such cellulosic fiber textiles, however, suffer from shrinkage after washing and hand-and-feel hardening after repetitive washing.
  • the cause of the shrinkage after washing is correlated to two phenomena.
  • One phenomenon is the deformation of woven and knitted goods by various forces applied during their manufacture and treatment. More particularly, as washing causes woven and knitted goods to be tossed and turned in a free state without the application of force, they tend to resume their original stable state, inviting shrinkage.
  • Such shrinkage can be prevented by mechanical methods such as is typified by sanforization.
  • the method using a sanforizing machine of the rubber belt or felt blanket type is to impart shrink-proofness by physically and continuously compressing the fabric for contraction to reduce the shrinkage potential of the fabric.
  • the method cannot achieve a full reduction of the shrinkage potential of thick fabric pieces or hard finished fabrics.
  • the other phenomenon is the shrinkage of woven and knitted goods as a result of individual fibers absorbing water to swell and to increase their cross-sectional area. This shrinkage occurs upon the absorption of water. After the fabric is dried to remove the water, the fabric tissue cannot recover its original size prior to swelling by itself. The fabric remains shrunk.
  • An object of the present invention is to provide a method for treating a cellulosic fiber textile to be fully shrink-proof without a substantial loss of strength so that it may experience minimal shrinkage after washing and minimal hand-and-feel hardening after repetitive washing.
  • the cellulosic fiber textile can be rendered fully shrink-proof so that it may experience minimal shrinkage after washing and minimal hand-and-feel hardening after repetitive washing. This is accomplished without a substantial loss of strength.
  • liquid ammonia penetrates into not only the amorphous regions, but also the crystalline regions of the cellulose to break down the hydrogen bonds so that the fibers in their entirety are swollen. Thereafter, heat treatment is carried out to evaporate the liquid ammonia whereupon hydrogen bonds are newly formed and a cellulose III crystalline structure is created at least partially in the crystalline region. The crystals are fixed in a swollen state. This results in a lower crystallinity. When such a fabric is given a resin finish, the crease and shrink-proof properties are improved with a slight loss of strength. This fact is well known in the art.
  • Subsequent resin treatment on the thus treated cellulosic fiber textile can impart improved crease or shrink-proof properties without a substantial loss of strength when compared with the prior art resin treatment.
  • the prior art resin treatment of a cellulosic fiber textile has the tendency that as the amount of resin added increases, the crease or shrink-proof properties are improved, but the tensile strength is reduced at the same time.
  • An improvement in the crease or shrink-proof properties is achieved by introducing crosslinks between the cellulosic fibers to stabilize the hydrogen bonds while a lowering of the tensile strength occurs because of the introduction of crosslinks which invite the likelihood of local brittle fracture. These are contradictory to each other. It is desired to find a compromise between the shrink-proof improvement and strength loss. Since cellulosic fibers have a heterogeneous structure including crystalline and amorphous portions or skin and interior portions, it is desired to achieve a uniform distribution of the crosslinking sites in order to prevent strength lowering.
  • the shrink-proof treatment method of the present invention is successful in producing a fully shrink-proof cellulosic fiber textile, without a substantial loss of strength, which experiences minimal shrinkage after washing and minimal hand-and-feel hardening after repetitive washing. Especially, improved crease or shrink-proof properties can be imparted to even such thin, low strength fabrics made of cotton, linen, rayon, etc. while maintaining a practically acceptable strength.
  • the present invention provides a method for the shrink-proof treatment of a cellulosic fiber textile, comprising the steps of treating the fiber textile with liquid ammonia, then treating the fiber textile under tension or under no tension with hot water or a caustic alkali, and optionally treating the fiber textile with a resin.
  • FIG. 1 is a graph showing the dry crease-proof property vs. the tensile strength of the fabric pieces treated in Example 18 and Comparative Example 15.
  • FIG. 2 is a graph showing the dry crease-proof property vs. the tensile strength of the fabric pieces treated in Example 19 and Comparative Example 16.
  • FIG. 3 is a graph showing the dry crease-proof property vs. the tensile strength of the fabric pieces treated in Example 20 and Comparative Example 17.
  • FIG. 4 is a graph showing the dry crease-proof property vs. the tensile strength of the fabric pieces treated in Example 21 and Comparative Example 18.
  • FIG. 5 is a graph showing the dry crease-proof property vs. the tensile strength of the fabric pieces treated in Example 22 and Comparative Example 19.
  • FIG. 6 is a graph showing the dry crease-proof property vs. the tensile strength of the fabric pieces treated in Example 23 and Comparative Example 20.
  • the shrink-proof treatment method of the invention involves the step (1) of treating a cellulosic fiber textile with liquid ammonia, and the step (2) of treating the fiber textile under tension or under no tension with hot water or a caustic alkali.
  • a cellulosic fiber textile which can be processed by the method of the invention is composed of cellulosic fibers including natural fibers and regenerated cellulose fibers, for example, cotton, hemp, rayon, polynosics, cuprammonium fibers, and high-strength regenerated cellulose fibers (available under the trade name of Tencel, for example).
  • These natural fibers and regenerated cellulose fibers may take the form of composite fibrous materials obtained by blending with other fibers such as synthetic fibers, typically polyesters and polyamides.
  • the composite fibrous materials should preferably have a greater content of cellulosic fibers, more preferably a cellulosic fiber content of at least 50% by weight.
  • the alkali treatment can be applied only to fibers which are insoluble in the alkali solution to be used.
  • the cellulosic fiber textile which can be used herein includes woven fabrics, knitted goods and non-woven fabrics. If desired, the textile may be subjected to pretreatment such as singeing, desizing, scouring, bleaching, and mercerizing. Also, the textile may have been dyed or printed.
  • the cellulosic fiber textile is treated with liquid ammonia, for example, by impregnating the textile with liquid ammonia kept at a temperature of -33°C or lower under atmospheric pressure.
  • the said impregnating means include dipping in liquid ammonia, spraying of liquid ammonia, and coating of liquid ammonia.
  • the said impregnating time may be properly selected in the range of about 5 to 40 seconds.
  • Liquid ammonia is most often used to induce a transition of cellulose I or II in the cellulosic fiber textile into cellulose III, although lower alkylamines such as methylamine and ethylamine may be used if desired.
  • the ammonia is removed from the liquid ammonia-treated cellulosic fiber textile by heating.
  • the liquid ammonia treatment causes the cellulose I or II crystalline structure to convert to the cellulose III crystalline structure in proportion to the impregnating time.
  • the content of cellulose III crystalline structure based on the entire crystals reaches about 10% at an impregnating time of 5 seconds, about 15% at 8 seconds, about 25% at 12 seconds, about 35% at 18 seconds, and about 40% at 20 seconds or longer.
  • the content of cellulose III crystalline structure is less than 40%, more preferably 10 to 35% based on the entire crystals when hot water treatment is carried out subsequent to the liquid ammonia treatment. No satisfactory shrink-proofness would be expectable with a cellulose III content of less than 10% whereas hand-and-feel would become hard with a cellulose III content of 40% or more.
  • the cellulosic fiber textile having a cellulose III crystalline structure created by the liquid ammonia treatment is subjected to hot water treatment or a caustic alkali treatment while it is kept under tension or under no tension, thereby causing a transition of at least a part of the cellulose III crystalline structure in the cellulosic fiber textile into a cellulose I or II crystalline structure.
  • At least a part of the cellulose III crystalline structure is converted into a cellulose I or II crystalline structure by either of the following procedures of: (a) first converting the cellulose I crystalline structure of the native cellulose into cellulose III through liquid ammonia treatment and converting it back to cellulose I through hot water treatment; (b) first converting the cellulose II crystalline structure of regenerated cellulose into cellulose III through liquid ammonia treatment and converting it back to cellulose II through hot water treatment; (c) first converting the cellulose I crystalline structure of the native cellulose into cellulose II through mercerization, then converting it into cellulose III through liquid ammonia treatment and converting it back to cellulose II through hot water treatment; and (d) first converting the cellulose I or II crystalline structure of the native cellulose into cellulose III through liquid ammonia treatment and converting it to cellulose II through caustic alkali treatment.
  • the crystalline state of the final product is a mixture of the cellulose crystalline states created in the steps it has passed through.
  • Hot water treatment is carried out by dipping the cellulosic fiber textile in hot water at a temperature of 100 to 150°C, preferably 110 to 140°C. More particularly, an apparatus capable of hot water treatment under high pressure is used.
  • hot water treatment is carried out by high-pressure liquid flow dyeing machines, high-pressure paddle dyeing machines, high-pressure jigger dyeing machines, high-pressure drum dyeing machines, or high-pressure beam dyeing machines.
  • the time of such hot water treatment varies with the temperature of the hot water and the like although it is generally about 10 minutes to about 5 hours, preferably about 20 minutes to about 4 hours.
  • An appropriate time is at least 2 hours at 100°C, at least 1 hour at 110°C, at least 40 minutes at 120°C, and at least 20 minutes at 130°C.
  • the hot water treatment causes at least a portion, preferably at least 25%, more preferably at least 40% of the cellulose III crystalline structure in the fiber textile to convert back to the cellulose I or II crystalline structure. More particularly, when the crystalline structure is converted from cellulose I to cellulose III by the liquid ammonia treatment, it can be converted back to cellulose I by the hot water treatment. When started from cellulose II, the crystalline structure can be converted back to cellulose II by the hot water treatment.
  • the percent conversion of cellulose III to cellulose I or II is calculated according to ⁇ (a percent content of cellulose III in the entire crystals prior to hot water treatment) - (a percent content of cellulose III in the entire crystals subsequent to hot water treatment) ⁇ /(a percent content of cellulose III in the entire crystals prior to hot water treatment) x 100% .
  • Hot water treatment is carried out while the textile is kept either under tension or under no tension.
  • hot water treatment is carried out using a high-pressure liquid flow dyeing machine, a high-pressure drum dyeing machine or a high-pressure paddle dyeing machine while the textile is kept under no tension.
  • hot water treatment is carried out using a high-pressure beam dyeing machine or a high-pressure jigger dyeing machine while the textile is kept in a flat state (or under tension).
  • the hot water treatment is applicable to dyed and printed textiles.
  • the cellulosic fiber textile is dyed or printed prior to hot water treatment. Since hot water treatment need not use basic or acidic aids such as caustic soda and acetic acid, the hot water treatment of dyed and printed textiles does not detract from the color or dye fastness. Due to the eliminated need for a resin finish, little lowering of the strength occurs.
  • the hot water treatment of a cellulosic fiber textile at a zero tension, in a relaxed state yields shrink-proof natural cellulose fiber woven fabrics having a percent warp wash-shrinkage after 10 cycles of washing of up to 1.5% for cotton fabric, up to 2.0% for linen fabric, and up to 2.0% for ramie fabric.
  • shrink-proof natural cellulose fiber knitted goods such as single tuck cotton knitted goods having a total percent warp/weft wash-shrinkages after 10 cycles of washing of up to 15.0%.
  • shrink-proof regenerated cellulose fiber woven fabrics having a percent warp wash-shrinkage after 10 cycles of washing of up to 3.0% for rayon spun fabric, up to 3.5% for rayon filament x rayon spun fabric and up to 2.0% for cuprammonium rayon fabric. It is noted that the percent shrinkage is determined by washing a fabric according to the JIS L-217 103 method, followed by tumble drying.
  • the cellulosic fiber textile is subjected to caustic alkali treatment.
  • the caustic alkali treatment is done on the cellulosic fiber textile which is kept under tension or under no tension.
  • Caustic alkali treatment is carried out using well known apparatus such as mercerizing machines. More particularly, the cellulosic fiber textile is impregnated with an aqueous solution of a caustic alkali, thereby converting at least a part of the cellulose III crystalline structure into a cellulose II crystalline structure.
  • the caustic alkali used herein is typically sodium hydroxide (NaOH) or potassium hydroxide (KOH), with sodium hydroxide being preferred. Other alkaline chemicals may be used if necessary.
  • the textile is treated with an aqueous solution of caustic alkali having a caustic alkali concentration of 0.1 to 40% by weight at a temperature of -10°C to 150°C for about 20 seconds to about 24 hours.
  • caustic alkali treatment is carried out using a caustic alkali aqueous solution at temperatures of 90°C or less, which treatment is referred to as low-temperature alkali treatment, hereinafter, the solution should preferably have a caustic alkali concentration of 10 to 40%, more preferably 15 to 40%, most preferably 15 to 30% by weight.
  • An appropriate treating temperature is -10°C to 90°C, more preferably 10°C to 40°C.
  • the time of caustic alkali treatment need not be specifically determined since it varies with the concentration and temperature of the caustic alkali solution. The treating time is typically about 20 seconds to 24 hours.
  • caustic alkali treatment is carried out using a caustic alkali aqueous solution at temperatures of higher than 90°C, which treatment is referred to as high-temperature alkali treatment, hereinafter, the solution should preferably have a caustic alkali concentration of 0.1 to 10%, more preferably 0.2 to 5% by weight.
  • An appropriate treating temperature is more than 90°C to 150°C, more preferably 100°C to 150°C, most preferably 110°C to 140°C.
  • the time of caustic alkali treatment need not be specifically determined since it varies with the concentration and temperature of the caustic alkali solution.
  • the treating time is typically about 1 minute to about 5 hours, preferably 10 minutes to 5 hours, more preferably 20 minutes to 3 hours.
  • the caustic alkali treatment would become ineffective if the caustic alkali concentration is too low. If the caustic alkali concentration is too high, no further improvement is recognized and there would result the drawback that a subsequent neutralizing step to remove the caustic alkali requires a more time and cost.
  • the above-mentioned low- and high-temperature alkali treatments can be done while the cellulosic fiber textile is kept under tension or under no tension.
  • the amount of caustic alkali aqueous solution applied to the cellulosic fiber textile is preferably at least 50% by weight of a portion of the cellulosic fiber textile to be impregnated.
  • a mangle padder may be used.
  • a printing machine as used in printing techniques may be used.
  • the cellulosic fiber textile can be dyed or printed prior to the application of the caustic alkali aqueous solution.
  • the caustic alkali treatment is carried out while the cellulosic fiber textile is kept under tension or under no tension.
  • the caustic alkali treatment is carried out using a liquid flow dyeing machine, a drum dyeing machine or a paddle dyeing machine while the textile is kept under no tension.
  • the caustic alkali treatment is carried out using a mercerizing machine, a high-pressure beam dyeing machine or a high-pressure jigger dyeing machine while the textile is kept under tension.
  • the caustic alkali treatment under no tension gives the same advantages as achieved with the hot water treatment.
  • the caustic alkali treatment under tension using a mercerizing machine has the advantages that no creases or irregularities are introduced into the textile and the selvage is not rolled since the textile is kept flat during the caustic alkali treatment, and treatment on a mass scale is possible.
  • the treating time is usually about 20 to 80 seconds.
  • the thus caustic alkali treated cellulosic fiber textile is then treated with an acid for neutralizing the alkali and washed with water.
  • the acid used herein includes inorganic acids such as sulfuric acid and hydrochloric acid and organic acids such as acetic acid and formic acid.
  • the above-mentioned method involving liquid ammonia treatment and subsequent hot water or caustic alkali treatment has several advantages. Since resin as typified by formaldehyde are not used at all, no formaldehyde is left in the textile. A fully shrink-proof cellulosic fiber textile which experiences minimal shrinkage after washing and minimal hand-and-feel hardening after repetitive washing is obtained without a substantial loss of strength.
  • the invention is effective for imparting good shrink-proofness to pieces of thick fabric or hard finished fabric as well as giving an improved luster and dyeing density.
  • the resin used herein is any of the compounds that react with a hydroxyl group of cellulose to form a crosslink, for example, aldehydes such as formaldehyde, glyoxal, and glutaraldehyde, epoxy compounds such as diglycidyl ether, polycarboxylic acids such as tetrabutane-carboxylic acid, and cellulose reactive N-methylol compounds such as dimethylol urea, trimethylol melamine, dimethylol ethylene urea, and dimethylol dihydroxy ethylene urea.
  • aldehydes such as formaldehyde, glyoxal, and glutaraldehyde
  • epoxy compounds such as diglycidyl ether
  • polycarboxylic acids such as tetrabutane-carboxylic acid
  • cellulose reactive N-methylol compounds such as dimethylol urea, trimethylol melamine, dimethylol ethylene urea, and dimethyl
  • An appropriate amount of such a resin added is 1 to 10% by weight, especially 2 to 6% by weight calculated as solids based on the weight of the cellulosic fiber textile to be treated therewith. Less than 1% of the resin would be less effective for a resin finish whereas more than 10% of the resin would induce a substantial loss in strength.
  • reaction of the cellulosic fiber textile with formaldehyde in the vapor phase which is known as the VP reaction
  • VP reaction reaction of the cellulosic fiber textile with formaldehyde in the vapor phase
  • the amount of formaldehyde added is preferably 0.1 to 3% by weight calculated as solids based on the weight of the cellulosic fiber textile. This is because if formaldehyde having a smaller molecular weight than the N-methylol compounds is added in the same amount as the N-methylol compounds, too much crosslinking is introduced and causes a drop in strength. Less than 0.1% of formaldehyde would be less effective for the resin finish whereas more than 3% of formaldehyde would induce a substantial drop in strength.
  • a catalyst may be added for increasing the reactivity of the resin with the cellulose to achieve rapid resin treatment.
  • the catalyst used herein is any of the catalysts commonly used for resin treatment, for example, borofluorides such as ammonium borofluoride, sodium borofluoride, potassium borofluoride, and zinc borofluoride, neutral metal salt catalysts such as magnesium chloride, magnesium sulfate and magnesium nitrate, and inorganic acids such as phosphoric acid, hydrochloric acid, sulfuric acid, sulfurous acid, hyposulfurous acid, and boric acid.
  • the catalyst is combined with a co-catalyst, for example, organic acids such as citric acid, tartaric acid, malic acid, and maleic acid.
  • an auxiliary agent is added to the resin for ensuring a smooth reaction of the resin with the cellulose. That is, the auxiliary agent functions to promote the reaction of the resin with the cellulose, to render the crosslinking reaction uniform as a reaction solvent, and to swell the cellulose.
  • auxiliary agents include polyhydric alcohols such as glycerin, ethylene glycol, polyethylene glycol, and polypropylene glycol; ether alcohols such as ethylene glycol monoethyl ether, diethylene glycol monoethyl ether, ethylene glycol monomethyl ether, diethylene glycol monomethyl ether, and diethylene glycol monobutyl ether; nitrogenous solvents such as dimethylformamide, morpholine, 2-pyrrolidone, dimethylacetamide, and N-methylpyrrolidone; and esters such as ethyl acetate, isopropyl acetate, butyl acetate, amyl acetate, ethylene glycol monomethyl ether acetate, ethylene glycol monoethyl ether acetate and ⁇ -butyrolactone.
  • polyhydric alcohols such as glycerin, ethylene glycol, polyethylene glycol, and polypropylene glycol
  • ether alcohols such as ethylene glycol monoeth
  • additives can be added to the resin if desired, for example, softeners for hand-and-feel adjustment and formaldehyde scavengers for reducing the concentration of free formaldehyde.
  • Any desired method may be used to apply the resin to the cellulosic fiber textile.
  • a choice may be made from among the well-known methods such as pad drying and the vapor phase (VP) reaction of formaldehyde.
  • the pad drying method involves dipping a piece of the fabric in a liquid preparation of the resin, squeezing the fabric at a squeeze rate of 50 to 120%, and drying the fabric at an ambient temperature of about 70 to 100°C to remove the water.
  • a long drying time is required at an ambient temperature below 70°C whereas at an ambient temperature above 100°C, migration of the resin can occur, resulting in a non-uniform distribution of the resin.
  • the cellulose together with the resin is heat treated at a temperature of 120 to 170°C, especially 130 to 160°C for 1 to 15 minutes, especially 2 to 10 minutes, to induce crosslinking.
  • the temperature and time of heat treatment vary with the type and amount of resin, the type and amount of catalyst, and the like. Reaction would be slow at a heat treating temperature of less than 120°C whereas a heat treating temperature of higher than 170°C would cause yellowing of the fabric.
  • the VP reaction method uses formaldehyde as the resin and applies formaldehyde in the vapor phase to the fabric.
  • a softener, polyethylene glycol, etc. are previously applied to the fabric by the pad drying method or the like.
  • the fabric is placed in a closed container, into which formaldehyde and an acidic gas such as sulfur dioxide are introduced whereby the fabric adsorbs the gaseous compounds.
  • the fabric is then heated to induce crosslinking.
  • the amount of formaldehyde bonded is about 0.1 to 3% by weight of the fabric, the temperature is 20 to 160°C and the treating time is about 1 to 60 minutes.
  • the amount of resin added can be extremely reduced as compared with the conventional resin treatment, which contributes to a reduced drop in the fabric strength.
  • a more crease or shrink-resistant cellulosic fiber textile is obtained. Even in the case of such thin, low strength fabrics as cotton, linen and rayon, a high degree of crease or shrink-proofing can be imparted while maintaining a practically acceptable strength.
  • the cellulosic fiber textile may be subjected to a final finishing treatment such as tentering and hand-and-feel adjustment.
  • a plain weave cotton 100% fabric of 50-count single yarn (warp density 148 yarns/inch, weft density 80 yarns/inch) was conventionally bleached, treated with liquid ammonia for 10 seconds, and heated to evaporate the ammonia.
  • the fabric was then treated with hot water under no tension at 130°C for 2 hours by means of a high-pressure liquid flow dyeing machine, followed by dewatering, drying, and tentering.
  • Example 1 Treatment as in Example 1 was done on a plain weave linen 100% fabric of 60-count single yarn (warp density 60 yarns/inch, weft density 52 yarns/inch).
  • Example 1 Treatment as in Example 1 was done on a plain weave ramie 100% fabric of 60-count single yarn (warp density 52 yarns/inch, weft density 56 yarns/inch).
  • Example 1 Treatment as in Example 1 was done on an ordinary single tuck cotton knit obtained by knitting 40-count two-folded yarns of cotton by a knitting machine with a cylinder diameter of 30 inches and a needle density of 18 needles/inch.
  • Example 1 The procedure of Example 1 was repeated except that the liquid ammonia treatment was omitted.
  • Example 2 The procedure of Example 2 was repeated except that the liquid ammonia treatment was omitted.
  • Example 3 The procedure of Example 3 was repeated except that the liquid ammonia treatment was omitted.
  • Example 4 The procedure of Example 4 was repeated except that the liquid ammonia treatment was omitted.
  • the woven and knitted fabrics of Examples 1 to 4 and Comparative Examples 1 to 4 were subjected to a washing test (JIS L-217 103 method) involving 1 cycle of washing or 10 cycles of washing, followed by tumble drying.
  • the woven fabric was measured for its warp shrinkage.
  • For the knit fabric the sum of the warp and weft shrinkages was determined. The results are shown in Table 1.
  • a plain weave spun rayon 100% fabric of 30-count single yarn (warp density 68 yarns/inch, weft density 60 yarns/inch) was conventionally bleached, treated with liquid ammonia for 10 seconds, and heated to evaporate the ammonia.
  • the fabric was then treated with hot water under no tension at 130°C for 2 hours by means of a high-pressure liquid flow dyeing machine, followed by dewatering, drying, and tentering.
  • Example 5 Treatment as in Example 5 was done on a plain weave warp rayon filament fabric of 120-denier rayon filaments as the warp (warp density 120/inch) and 30-count single yarn rayon staples as the weft (weft density 60/inch).
  • Example 5 Treatment as in Example 5 was done on a plain weave cuprammonium rayon 100% fabric of 75-denier cuprammonium rayon filaments as the warp (warp density 144/inch) and 120-denier cuprammonium rayon filaments as the weft (weft density 87/inch).
  • Example 5 The procedure of Example 5 was repeated except that the liquid ammonia treatment was omitted.
  • Example 6 The procedure of Example 6 was repeated except that the liquid ammonia treatment was omitted.
  • Example 7 The procedure of Example 7 was repeated except that the liquid ammonia treatment was omitted.
  • the woven fabrics of Examples 5 to 7 and Comparative Examples 5 to 7 were subjected to a washing test (JIS L-217 103 method) involving 1 cycle of washing or 10 cycles of washing, followed by tumble drying.
  • the woven fabric was measured for its warp shrinkage.
  • Table 2 Rayon spun woven fabric Rayon filament x rayon spun woven fabric Cuprammonium rayon woven fabric E5 CE5 E6 CE6 E7 CE7 Warp shrinkage (%) 1 cycle of washing 1.4 5.8 2.5 23.0 1.0 6.5 10 cycles of washing 2.0 7.3 3.0 25.0 1.5 9.5
  • a 7-count cotton denim 100% woven fabric (warp density 65 yarns/inch, weft density 43 yarns/inch) was impregnated with liquid ammonia at -34°C for 10 seconds, heated to evaporate the ammonia, desized conventionally, and then treated with hot water in a flat state at 130°C for 2 hours by means of a high-pressure beam dyeing machine, followed by tentering.
  • Example 8 Treatment as in Example 8 was done on an 8-count cotton/rayon (40/60) mix denim 100% woven fabric (warp density 69 yarns/inch, weft density 43 yarns/inch).
  • Example 8 Treatment as in Example 8 was done on a Tencel denim 100% woven fabric of 21-count warp yarn (warp density 115 yarns/inch) and 10-count weft yarn (weft density 54 yarns/inch).
  • Example 8 The procedure of Example 8 was repeated except that the hot water treatment was omitted.
  • Example 9 The procedure of Example 9 was repeated except that the hot water treatment was omitted.
  • Example 10 The procedure of Example 10 was repeated except that the hot water treatment was omitted.
  • the fabric was washed 1, 5 and 10 cycles according to JIS L-1096 F-2 method, followed by tumble drying. The fabric was measured for its warp and weft shrinkage.
  • the weft tensile strength was measured according to JIS L-1096.
  • a cotton 100% woven fabric of 80-count two-folded yarn plain weave (warp density 149 yarns/inch, weft density 62 yarns/inch) was conventionally bleached, impregnated with liquid ammonia at -34°C for 10 seconds, and heated to evaporate the ammonia.
  • the fabric was then impregnated under tension with a 20 wt% caustic alkali at 25°C for 60 seconds, neutralized, and washed with water, followed by dewatering, drying and tentering.
  • Example 11 The procedure of Example 11 was repeated except that the liquid ammonia treatment was omitted.
  • Example 11 The procedure of Example 11 was repeated except that the caustic alkali treatment was omitted.
  • Example 11 The woven fabrics of Example 11 and Comparative Examples 11 and 12 were examined for their shrinkage and tensile strength as in Example 8. The results are shown in Table 4.
  • Table 4 E11 CE11 CE12 Warp Weft Warp Weft Warp Weft Shrinkage (%) 1 cycle of washing 0.7 1.5 1.3 2.2 1.1 2.7 5 cycles of washing 0.7 1.8 2.0 2.2 1.6 3.1 10 cycles of washing 1.1 1.8 2.4 2.5 1.8 3.3 Weft tensile strength (kgf) 42.3 39.0 39.4
  • a 40-count two-folded yarn single tuck (30 inches x 18 gauge) cotton 100% knit was conventionally bleached and mercerized, impregnated with liquid ammonia at -34°C for 10 seconds, and heated to evaporate the ammonia.
  • the fabric was then impregnated with a 16 wt% caustic alkali at 25°C for 50 seconds, neutralized, and washed with water, followed by dewatering, drying and tentering.
  • Example 12 The procedure of Example 12 was repeated except that the mercerizing treatment was omitted.
  • Example 12 The procedure of Example 12 was repeated except that the caustic alkali treatment was omitted.
  • Example 13 The procedure of Example 13 was repeated except that the caustic alkali treatment was omitted.
  • a plain weave cotton 100% fabric of 40-count single yarn (warp density 132 yarns/inch, weft density 71 yarns/inch) was conventionally bleached, impregnated with liquid ammonia at -34°C for 10 seconds, and heated to evaporate the ammonia.
  • the fabric was then impregnated under no tension with a caustic alkali solution having an alkali concentration and a temperature as shown in Table 6 for a time as shown in Table 6, neutralized, and washed with water, followed by dewatering, drying and tentering.
  • Example 14 to 17 were examined for shrinkage and tensile strength as in Example 1. The results are shown in Table 6. Table 6 E14 E15 E16 E17 Caustic treatment 130°Cx2hr. 130°Cx2hr. 130°Cx2hr. 130°Cx2hr. 130°Cx2hr.
  • a cotton 100% plain weave fabric (warp: 50 count, density 148 yarns/inch, weft: 50 count, density 80 yarns/inch) was impregnated with liquid ammonia at -34°C for 20 seconds, heated to evaporate the ammonia, and then treated with hot water at 130°C for 1 hour in a flat state by means of a high-pressure beam dyeing machine.
  • the fabric was subjected to resin treatment by preparing a resin solution according to the formulation shown in Tables 7 and 8 and applying it by a pad drying method.
  • the resin treatment included the application of the resin solution by a mangle with a squeeze rate set at 60%, pre-drying at 85°C for 15 minutes, and heat treatment under the conditions as shown in Tables 7 and 8.
  • the thus obtained fabrics of Examples 18 and 19 were examined for their dry crease-proof property and tensile strength.
  • the results are shown in Tables 7 and 8.
  • the relationship of the tensile strength to the dry crease-proof property is shown in FIGS. 1 and 2. It is noted that the fabric was measured for its tensile strength and dry crease-proof property according to JIS L-1096.
  • Zinc borofluoride Aqueous solution of 45% zinc borofluoride by Morita Chemical K.K. *4 Sumitex buffer FW: Formaldehyde scavenger by Sumitomo Chemical K.K. *5 Meikatex PE-140: Polyethylene softener by Meisei Chemical K.K. *6 PEG200: Polyethylene glycol by Sanyo Chemicals K.K.
  • the resin solution was prepared by adding water to the chemicals of the formulation shown in Tables 7 and 8 to a total volume of 100 ml.
  • Example 18 A cotton 100% plain weave fabric as used in Example 18 was impregnated with liquid ammonia at -34°C for 10 seconds, heated to evaporate the ammonia, treated under no tension with hot water at 130°C for 1 hour by means of a high-pressure liquid flow dyeing machine, and finally resin finished using the resin formulation and conditions shown in Table 9.
  • the thus treated fabric of Example 20 was measured for its physical properties as in Example 18. The results are shown in Table 9 and FIG. 3.
  • Zinc borofluoride Aqueous solution of 45% zinc borofluoride by Morita Chemical K.K. *4 Sumitex buffer FW: Formaldehyde scavenger by Sumitomo Chemical K.K. *5 Meikatex PE-140: Polyethylene softener by Meisei Chemical K.K. *6 PEG200: Polyethylene glycol by Sanyo Chemicals K.K.
  • Example 18 A cotton 100% plain weave fabric as used in Example 18 was impregnated with liquid ammonia at -34°C for 20 seconds, heated to evaporate the ammonia, treated under tension with 20 wt% caustic soda at 25°C for 60 seconds by means of a conventional mercerizing machine, and finally resin finished using the resin formulation and conditions shown in Table 10.
  • the thus treated fabric of Example 21 was measured for its physical properties as in Example 18. The results are shown in Table 10 and FIG. 4.
  • Zinc borofluoride Aqueous solution of 45% zinc borofluoride by Morita Chemical K.K. *4 Sumitex buffer FW: Formaldehyde scavenger by Sumitomo Chemical K.K. *5 Meikatex PE-140: Polyethylene softener by Meisei Chemical K.K. *6 PEG200: Polyethylene glycol by Sanyo Chemicals K.K.
  • a linen 100% plain weave fabric (warp: hemp, 60 count, density 60 yarns/inch, weft: hemp, 60 count, density 52 yarns/inch) was impregnated with liquid ammonia at -34°C for 10 seconds, heated to evaporate the ammonia, treated under no tension with hot water at 130°C for 1 hour by means of a high-pressure liquid flow dyeing machine, and finally resin finished using the resin formulation and conditions shown in Table 11.
  • the thus treated fabric of Example 22 was measured for its physical properties as in Example 18. The results are shown in Table 11 and FIG. 5.
  • Zinc borofluoride Aqueous solution of 45% zinc borofluoride by Morita Chemical K.K. *4 Sumitex buffer FW: Formaldehyde scavenger by Sumitomo Chemical K.K. *5 Meikatex PE-140: Polyethylene softener by Meisei Chemical K.K. *6 PEG200: Polyethylene glycol by Sanyo Chemicals K.K.
  • a rayon 100% plain weave fabric (warp: 30 count, density 68 yarns/inch, weft: 30 count, density 60 yarns/inch) was impregnated with liquid ammonia at -34°C for 10 seconds, and heated to evaporate the ammonia, treated under no tension with hot water at 130°C for 1 hour by means of a high-pressure liquid flow dyeing machine, and finally resin finished using the resin formulation and conditions shown in Table 12.
  • the thus treated fabric of Example 23 was measured for its physical properties as in Example 18. The results are shown in Table 12 and FIG. 6.
  • Comparative Example 20 was the same as Example 23 except that the hot water treatment was omitted.
  • Zinc borofluoride Aqueous solution of 45% zinc borofluoride by Morita Chemical K.K. *4 Sumitex buffer FW: Formaldehyde scavenger by Sumitomo Chemical K.K. *5 Meikatex PE-140: Polyethylene softener by Meisei Chemical K.K. *6 PEG200: Polyethylene glycol by Sanyo Chemicals K.K.
  • a cotton 100% plain weave fabric as used in Example 18 was impregnated with liquid ammonia at -34°C for 20 seconds, heated to evaporate the ammonia, and treated under no tension with hot water at 130°C for 1 hour by means of a high-pressure liquid flow dyeing machine.
  • a softener and polyethylene glycol as shown in Table 13 were previously applied to the fabric by a pad drying method, and a crosslinking reaction (VP reaction) was carried out in formaldehyde and sulfur dioxide gas at 50 to 120°C for 10 minutes. The amount of formaldehyde bonded was 0.3% by weight.
  • Example 24 The thus treated fabric of Example 24 was measured for its physical properties as in Example 18. The results are shown in Table 13.
  • Comparative Example 21 was the same as Example 24 except that the hot water treatment was omitted.
  • Table 13 E24 CE21 Hot water treatment High-pressure beam dyeing machine None Treating agent (g/100 ml) PE-140* 5 1 1 PEG200* 6 3 3 Fabric properties Tensile strength (kgf) 43.0 40.3 Dry crease-proof property (°) 258 246 *5 Meikatex PE-140: Polyethylene softener by Meisei Chemical K.K. *6 PEG200: Polyethylene glycol by Sanyo Chemicals K.K.
  • a 40-count two-folded yarn single tuck (30 inches x 18 gauge) cotton 100% knit was conventionally bleached, impregnated with liquid ammonia at -34°C for 20 seconds, heated to evaporate the ammonia, treated under no tension with hot water at 130°C for 1 hour by means of a high-pressure liquid flow dyeing machine, spin dried and heat dried. Resin treatment was then carried out by means of a tenter.
  • the treating resin formulation and conditions were the same as in Example 18.
  • the fabric was examined for the shrinkage (warp + weft) after washing and tumble drying according to JIS L-217 103 method and for its burst strength according to JIS L-1018 Mullen method. The results are shown in Table 14.
  • Comparative Example 22 was the same as Example 25 except that the fabric was washed under no tension with warm water at 60°C for 1 hour instead of the hot water treatment.
  • Table 14 Resin concentration 5% 10% 15% 20% E25 CE22 E25 CE22 E25 CE22 E25 CE22 Warp + weft shrinkage (%) 1 cycle of washing 10.3 13.5 6.8 9.8 4.3 7.3 2.5 4.1 5 cycles of washing 11.3 15.8 7.9 11.3 6.3 8.7 3.4 6.2 10 cycles of washing 11.5 16.4 8.0 12.4 6.7 9.5 4.5 7.3 Burst strength (kg/cm 2 ) 7.0 7.2 5.1 5.2 4.4 4.2 4.4 4.1
  • Example 25 The procedure of Example 25 was repeated except that the same knit fabric as in Example 21 was treated under tension with 16 wt% caustic soda at 25°C for an impregnating time of 50 seconds by means of a conventional mercerizing machine prior to the liquid ammonia treatment. The fabric was examined for its washing shrinkage (warp + weft) and its burst strength as in Example 25. The results are shown in Table 15.
  • Comparative Example 23 was the same as Example 26 except that the fabric was washed under no tension with warm water at 60°C for 1 hour instead of the hot water treatment.
  • Table 15 Resin concentration 5% 10% 15% 20% E26 CE23 E26 CE23 E26 CE23 E26 CE23 Warp + weft shrinkage (%) 1 cycle of washing 9.2 12.8 5.7 8.8 3.7 6.2 2.4 3.7 5 cycles of washing 10.4 14.9 6.7 10.1 5.7 7.6 3.3 5.5 10 cycles of washing 10.6 15.5 7.5 11.7 5.9 8.7 4.4 6.7 Burst strength (kg/cm 2 ) 8.3 8.3 6.2 6.1 5.2 5.2 5.1 4.8
  • Example 25 The procedure of Example 25 was repeated except that the same knit fabric as in Example 25 was treated under tension with 16 wt% caustic soda at 25°C for an impregnating time of 50 seconds by means of a conventional mercerizing machine instead of the hot water treatment. The fabric was examined for its washing shrinkage (warp + weft) and its burst strength as in Example 25. The results are shown in Table 16.
  • Comparative Example 24 was the same as Example 27 except that the mercerizing treatment was omitted.
  • Table 16 Resin concentration 5% 10% 15% 20% E27 CE24 E27 CE24 E27 CE24 E27 CE24 Warp + weft shrinkage (%) 1 cycle of washing 8.3 13.5 5.2 9.9 4.0 6.8 2.8 4.8 5 cycles of washing 9.2 15.1 6.5 11.2 5.5 7.5 3.5 6.2 10 cycles of washing 9.8 15.9 7.3 11.9 5.7 8.2 3.9 6.9 Burst strength (kg/cm 2 ) 8.3 6.5 7.4 5.8 6.2 4.7 5.5 4.3
  • improved crease or shrink-proof properties can be imparted to a cellulosic fiber-containing a structure without a substantial loss of fabric strength.
  • improved crease or shrink-proof properties can be imparted to even thin, low strength fabrics while maintaining a practically acceptable strength.
  • the balance of the fabric strength and the crease or shrink-proof properties are further improved so that improved shrink-proof properties can be imparted while minimizing the loss in fabric strength.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
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CN102517772A (zh) * 2011-12-30 2012-06-27 无锡市纳溪迩服饰有限公司 一种双面多彩针织面料的加工方法
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KARL BREDERECK: "Fixierung von Baumwollgewebe durch NaOH-Mercerisation und Flüssigammoniak-Behandlung", MELLIAND TEXTILBERICHTE, vol. 59, no. 8, August 1978 (1978-08-01), HEIDELBERG, pages 648 - 652, XP002039577 *
ZERONIAN S H ET AL: "THE EFFECT OF CROSS-LINKING WITH DIMETHYLOLDIHYDROXYETHYLENEUREA ON THE MECHANICAL PROPERTIES OF LIQUID-AMMONIA-TREATED COTTON FIBRES", JOURNAL OF THE TEXTILE INSTITUTE, vol. 81, no. 3, 1 January 1990 (1990-01-01), pages 310 - 318, XP000173579 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6203577B1 (en) * 1996-05-23 2001-03-20 Nisshinbo Industries, Inc. Shrink-proof treatment of cellulosic fiber textile
CN113152085A (zh) * 2021-05-21 2021-07-23 安徽弋尚纺织科技有限公司 一种抗皱效果好的复合面料的加工工艺

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CN1106477C (zh) 2003-04-23
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NO311676B1 (no) 2002-01-02
NO972309D0 (no) 1997-05-21

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