EP1100990B1 - Procede permettant de rendre un tissu infroissable et sans plis - Google Patents

Procede permettant de rendre un tissu infroissable et sans plis Download PDF

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Publication number
EP1100990B1
EP1100990B1 EP98921043A EP98921043A EP1100990B1 EP 1100990 B1 EP1100990 B1 EP 1100990B1 EP 98921043 A EP98921043 A EP 98921043A EP 98921043 A EP98921043 A EP 98921043A EP 1100990 B1 EP1100990 B1 EP 1100990B1
Authority
EP
European Patent Office
Prior art keywords
fabric
formaldehyde
cellulose
catalyst
heat curing
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
EP98921043A
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German (de)
English (en)
Other versions
EP1100990A4 (fr
EP1100990A1 (fr
Inventor
George L. Payet
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.)
Strike Investments LLC
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Strike Investments LLC
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
Priority claimed from US09/075,334 external-priority patent/US5885303A/en
Application filed by Strike Investments LLC filed Critical Strike Investments LLC
Publication of EP1100990A1 publication Critical patent/EP1100990A1/fr
Publication of EP1100990A4 publication Critical patent/EP1100990A4/fr
Application granted granted Critical
Publication of EP1100990B1 publication Critical patent/EP1100990B1/fr
Anticipated expiration legal-status Critical
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Classifications

    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • 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
    • 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
    • D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • D06M15/6436—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing amino groups
    • 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
    • D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • D06M15/657—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing fluorine
    • 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
    • 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
    • D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/20—Treatment influencing the crease behaviour, the wrinkle resistance, the crease recovery or the ironing ease

Definitions

  • This invention relates to a durable press/wrinkle-free process for cellulosic fiber-containing fabrics and more particularly to a process which permits high treatment level amounts of formaldehyde and catalysts to impart wrinkle resistance to the cellulosic fiber-containing fabrics while reducing the loss in both tensile and tear strength normally associated with such treatment processes.
  • the product may be isolated by washing and drying; preferably at a temperature of about 135.55°C (about 212°F).
  • the products obtained according to this process are said to show no increase in wet strength and possess a high water imbibition, an increased resistance to creasing and a slight increase in affinity to some direct dyes.
  • US 3,663,974 discloses a fabric comprising cellulose treated with aldehyde and optionally further agents, and as softeness.
  • US 3,420,696 discloses a process of treating cellulose with aldehyde and a carbonate.
  • GB 1,097,336 discloses a process for providing carpets with anti-soiling properties.
  • EP 0 360 248 A2 discloses a formaldehyde free process for treating textile fabrics.
  • This invention relates to a durable press/wrinkle-free process for cellulosic fiber containing fabrics and more particularly to a process which utilizes formaldehyde and catalysts with silicone elastomers to impart wrinkle resistance to the cellulosic fiber-containing fabrics while reducing loss in both tensile and tear strength. This process is particularly effective on 100% cotton fabric.
  • Such cellulosic fiber-containing fabrics include cloth made of cotton or cotton blends. There is a constant consumer demand for better treatment, that is, a more wrinkle-free product and for higher amounts of cotton in the blended fabric, or preferably, a 100% cotton fabric. There is a great demand for a wrinkle-free fabric made entirely of cotton and having good tensile and tear strength. This has been achieved and 100% cotton fabrics are treated today, but only in heavier weight pants or bottom weight fabrics. Unfortunately, the more wrinkle-free the cellulosic containing fabric is made by treatment in a formaldehyde system, the greater the loss in tear and tensile strength.
  • Polyester fibers are most often blended into the cotton to form a polyester cotton blend fabric to compensate for the loss in strength of the treated cotton. Polyester in amounts of up to 65% are commonly used. Because of the presence of polyester fibers or other synthetic fibers in the blend, these blended fabrics are sufficiently strong but do not have the comfort or feel of fabrics containing a higher amount of cotton, or most desirably, 100% cotton.
  • the process of the present invention overcomes the disadvantages of the prior art processes and permits the presence of higher percentages of cotton in the blend and even the treatment of lighter weight or shirting weight 100% cotton fabrics to a commercially acceptable wrinkle free standard while retaining adequate strength in the fabric to also make it commercially acceptable.
  • Commercial acceptability of the treated fabric is the ultimate goal of the process.
  • the durable press process of the present invention for treating cotton containing fabrics and 100% cotton fabric comprises treating a cellulosic fiber-containing fabric with aqueous formaldehyde and a catalyst capable of catalyzing the crosslinking reaction between formaldehyde and cellulose in the presence of a silicone elastomer, heat curing the treated cellulosic fiber-containing fabric, preferably having a moisture content of more than 20% by weight, under conditions at which formaldehyde reacts with the cellulose in the presence of a catalyst and without the substantial loss of formaldehyde before the reaction of formaldehyde with cellulose to improve the wrinkle resistance of the fabric while reducing the loss in both tensile and tear strength. It is preferable that the cellulose containing fabric is in the fully swollen state.
  • Silicone elastomers are known materials. Silicone elastomers have a backbone made of silicon and oxygen with organic substituents attached to silicon atoms comprising n repeating units of the general formula:
  • the groups R and R 1 may be the same or different and includes for example, lower alkyl, such as methyl, ethyl, propyl, phenyl or any of these groups substituted by hydroxy groups, fluoride atoms or amino groups; in other words, reactive groups to cellulose.
  • the silicones used to make the silicone elastomers in the present .invention are made by conventional processes which may include the condensation of hydroxy organosilicon compounds formed by hydrolysis of organosilicon halides.
  • the required halide can be prepared by a direct reaction between a silicon halide and a Grignard reagent . Alternate methods may be based on the reaction of a silane with unsatutrated compounds such as ethylene or acetylene. After separation of the reaction products by distillation, organosilicon halides may be polymerized by carefully controlled hydrolysis to provide the silicone polymers useful in the present invention.
  • elastomers may be made by polymerization of the purified tertramer using alkaline catalysts at 100 to 150°C (212-302 degrees F), the molecular weight being controled by using a monofuncfional silane. Curing characteristics and properties may be varied over a wide range by replacing some methyl groups by -H, -OH, fluoroalkly, alkoxy or vinyl groups and by compounding with flllers as would be appreciated by one of ordinary skill in the art.
  • Silicone elastomers used in the present invention are high weight materials, generally composed of dimethyl silicone units (monomers) linked together in a linear chain. These materials usually contain a peroxide type catalyst which causes a linking between adjacent methyl groups in the form of methylene bridges. The presence of crosslinking greatly improves the durability of the silicone elastomer on cellulose by producing larger molecules.
  • a reactive silicone elastomer which is one where reactive groups capable of reacting with the substrate have been added to the linear dimethyl silicone polymer.
  • These silicones are capable of reacting both with cellulose substrates as well as with most protein fibers, and are characterized by much greater durability of the silicone polymer on the substrate, even approaching the life of the substrate.
  • silicone elastomers which give off reaction gases or chemicals indicating chemical reaction with the substrate are much preferred over non reactive silicone elastomer, but this is not to say that non reactive silicone elastomers cannot be used in the process.
  • Different elastomers by different manufacturers have all shown increases in tensile as well as tear strength, as shown in Tables I and II included herein. Elastomeric silicone polymers have been found to increase strength whereas simple emulsified silicone oils (or lubricants) do not give increases in tensile strength.
  • the aqueous system containing formaldehyde, an acid catalyst, silicone elastomer and a wetting agent may be padded on the fabric to be treated, preferably to insure a moisture content of more than 20% by weight on the fabric, and then the fabric cured.
  • the padding technique is conventional to the art and generally comprises running the fabric through the aqueous solution which is then passed through squeezing rollers to provide a wet pick-up of about 66%.
  • the concentration of the reactants in the aqueous solution are adjusted to provide the desired amount of reactants on the weight of the fabric (OWF).
  • the padded fabric may be immediately plunged into a heating chamber at about 148,88°C to about 162,77°C (about 300 to about 325°F).
  • a heating chamber at about 148,88°C to about 162,77°C (about 300 to about 325°F).
  • This may also be accomplished by curing at a low temperature with an active catalyst. It is also possible to use any combination of techniques which prevent the substantial loss of formaldehyde during the curing. For example, a low temperature may be used in combination with an aqueous formaldehyde solution. It would also be possible to use a pressurized system wherein the pressure is greater than atmospheric, thereby preventing the substantial loss of formaldehyde before the formaldehyde crosslinks with the cellulosic fiber-containing fabric being treated.
  • the process of the present invention uses less formaldehyde than other known processes.
  • Shirting fabrics treated in accordance with the process of the present invention contain approximately 1000 ppm after treatment before steaming on a shirting fabric as compared to 3000 ppm+ by another crosslinking process on a similar shirting fabric.
  • Tests have shown that continuously running steaming chambers to which the treated fabric is exposed should effectively remove residual formaldehyde to concentrations as low as 200 ppm. This is also an important aspect of the present invention in view of consumers concern about the presence of formaldehyde in their purchased garments. It is also possible to wash fabrics either continuously or in batch washers. Both approaches remove essentially all of the formaldehyde.
  • additives may be a latex or fine aqueous dispersion of polyethylene, various alkyl acrylate polymers, acrytonitrile-butadiene copolymers, deacetylated ethylene-vinyl acetate copolymers, polyurethanes and the like.
  • Such additives are well known to the art and are generally commercially available in concentrated aqueous latex form.
  • Such a latex is diluted to provide about 1 to 3% polymer solids in the aqueous catalyst-containing padding bath before the fabric is treated therewith.
  • One known softener which was virtually the softener of choice in the durable press process using resin treatment or formaldehyde crosslinking was high density polyethylene, Mykon HD. It has been unexpectedly discovered that the substitution of a silicone elastomer for high density polyethylene significantly reduces the loss in tear strength of the treated fabric after washing as well as providing better control of the process as may be seen from the examples. The importance of good control of the process is essential to a commercially viable process to provide a consistent product from run to run which is not adversely affected by variations in atmospheric pressure, humidity and the like.
  • cellulosic fiber-containing fabric which may be treated by the present process there can be employed various natural cellulosic fibers and mixtures thereof, such as cotton and jute.
  • Other fibers which may be used in blends with one or more of the above-mentioned cellulosic fibers are, for example, polyamides (e.g., nylons), polyesters, acrylics (e.g., polyacrylonitrile), polyolefins, polyvinyl chloride, and polyvinylidene chloride.
  • Such blends preferably include at least 35 to 40% by weight, and most preferably at least 50 to 60% by weight, of cotton or natural cellulose fibers.
  • the fabric may be a resinated material but preferably it is unresinated; it may be knit, woven, non-woven, or otherwise constructed. After processing, the formed wrinkle resistant fabric will maintain the desired configuration substantially for the life of the fabric. In addition, the fabric will have an excellent wash appearance even after repeated washings.
  • This invention is not dependent upon the limited amounts of moisture to control the crosslinking reaction since the crosslinking reaction is most efficient in the most highly swollen state of the cellulose fiber. Lesser amounts of moisture may be used but are less preferred.
  • the silicone elastomer must be present in a sufficient amount to reduce the loss of tensile and tear strength in the fabric normally associated with the treatment of the same fabric in a prior art treatment process which may include the use of softeners such as Mykon HD.
  • the formulation and process of the present invention may be adjusted to meet specific commercial requirements for the treated fabric. For example, formaldehyde and the catalyst concentration may be increased to provide better treatment; then the concentration of the softener is also increased to combat the loss of tear strength caused by the increased amount of catalyst used in the process. This lends itself to computerized control of the systems for treating various fabrics and allows variation in the treatment of different fabrics, which is another advantage of the process of the present invention.
  • silicone oils are known as silicone softeners and have found some use in fabric treatment, they suffer serious disadvantages in having a strong tendency to produce non-removable spots.
  • silicone elastomer used in the process of the present invention completely overcomes these problems.
  • Blended fabrics to be treated in accordance with the present invention are immersed in a solution to provide a pick up or on the weight of fabric (OWF) of about 3 % formaldehyde, 1 % of catalyst, 1% of the silicone elastomer.
  • OPF weight of fabric
  • the curing temperature may be about 148,88°C (about 300°F).
  • the padded fabric may be plunged into a oven or heating chamber at 148,88°C (300°F).
  • the formaldehyde concentration may be varied as would be appreciated by one of ordinary skill in the art.
  • the process inlcudes the use of formaldehyde in the form of an aqueous solution having a concentration of 0.5% to 10%, by weight.
  • the preferred formaldehyde concentration on the fabric is from 1.5% to 7% based on the weight of the fabric.
  • the catalyst used in the process includes fluorosilicic acid for mild reactions and is applicable to blend fabrics.
  • a catalyst such as magnesium chloride spiked with citric acid can be used, which is a commercially available catalyst Freecat No. 9, as is a similar catalyst which contains aluminum/magnesium chloride.
  • moisture is given up from a high level, that is, greater than 20%, preferably greater than 30%, e.g., from 60-100% or more, and the crosslinking is optimized.
  • Moisture which is so difficult to control, is not a problem in the present invention. Of course, water is not allowed to be present in so much of an excess as to cause the catalyst to migrate on the fabric.
  • a visual comparative test is performed under controlled lighting conditions in which the amount of wrinkles in the treated fabric is compared with the amount of wrinkles present on pre-wrinkled plastic replicas.
  • the plastic replicas have various degrees of wrinkles and range from a value of 1 DP for a very wrinkled fabric to 5.0 DP for a flat wrinkle free fabric. The higher the DP value, the better. For a commercially acceptable wrinkle free fabric, a DP value of 3.5 is desired but rarely achieved. As would be appreciated by one of ordinary skill in the art, the difference between a DP of 3.50 and 3.25 is significant. At DP 3.50 all .wrinkles are rounded and disappearing.
  • non-ionic wetting agent was used as is conventional to the art.
  • the wetting agent was used in an amount of about 0.1% by weight.
  • the wetting agent used in all of the examples was an alkyl aryl polyether alcohol such as Triton X-100.
  • the wetting agent is used to cause complete wetting by the aqueous treating solution of the fibers in the fabric.
  • the silicone elastomer was the commercially available softener Sedgefield Elastomer Softener ELS, which is added as an opaque white liquid which contains from 24-26% silicone, has a pH of from 5.0-7.0 and is readily dilutable with water.
  • this product produced DP values at catalyst concentrations of 0.8%, whereas with the Mykon HD, a catalyst concentration of 2.0% was required to give a DP value of 3.50 after 1 washing and 3.25 after 5 washings.
  • the tensile strength with a catalyst concentration of 0.8% and tear strength are significantly and unexpectedly higher than the 2.0% catalyst required with Mykon HD to give equal DP results.
  • Catalyst concentration of 1.0% ELS is recommended to ensure a margin of safety, such that any variation in treatment will be well within accepted specifications.
  • Example 2 Another sample of the same fabric as used in Example 1 was padded with a similar solution differing only in that the catalyst Accelerator #9 was 1.0% OWF. Otherwise the sample was treated precisely the same.
  • Example 2 Another sample of the same fabric as used in Example 1 was padded with a similar solution differing only in that the catalyst Accelerator #9 was 2.0% OWF. Otherwise the sample was treated precisely the same.
  • Example 2 Another sample of the same fabric as used in Example 1 was padded with a similar solution differing only in that the catalyst Accelerator #9 was 0.4°C OWF, and Mykon HD was substituted for the Sedgesoft ELS elastomeric Softener. Otherwise the sample was treated precisely the same.
  • Example 2 Another sample of the same fabric as used in Example 1 was padded with a similar solution differing only in that the catalyst Accelerator #9 was 0.8% OWF, and Mykon HD was substituted for the Sedgesoft ELS elastomeric Softener. Otherwise the sample was treated precisely the same.
  • Example 2 Another sample of the same fabric as used in Example 1 was padded with a similar solution differing only in that the catalyst Accelerator #9 was 1.0% OWF, and Mykon HD was substituted for the Sedgesoft ELS elastomeric Softener Otherwise the sample was treated precisely the same.
  • Example 2 Another sample of the same fabric as used in Example 1 was padded with a similar solution differing only in that the catalyst Accelerator #9 was 1.5% OWF, and Mykon HD was substituted for the Sedgesoft ELS elastomeric Softener. Otherwise the sample was treated precisely the same.
  • Example 2 Another sample of the same fabric as used in Example 1 was padded with a similar solution differing only in that the catalyst Accelerator #9 was 2.0% OWF, and Mykon HD was substituted for the Sedgesoft ELS elastomeric Softener Otherwise the sample was treated precisely the same.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Claims (11)

  1. Procédé pour conférer une résistance durable au froissement à des tissus contenant des fibres cellulosiques, comprenant le traitement d'un tissu contenant des fibres cellulosiques par du formaldéhyde, un catalyseur apte à catalyser la réaction de réticulation entre le formaldéhyde et la cellulose, et une quantité efficace d'élastomère de silicone, le durcissement à chaud dudit tissu traité contenant des fibres cellulosiques dans des conditions dans lesquelles le formaldéhyde réagit avec la cellulose en présence du catalyseur et de l'élastomère de silicone, sans perte substantielle de formaldéhyde avant la réaction du formaldéhyde avec la cellulose, afin d'améliorer la résistance au froissement du tissu tout en réduisant la perte de résistance à la traction et à la déchirure.
  2. Procédé selon la revendication 1, dans lequel le durcissement à chaud est effectué à une température qui empêche la perte substantielle de formaldéhyde pendant le durcissement.
  3. Procédé selon la revendication 1, dans lequel l'étape de durcissement à chaud est effectuée à une température suffisamment élevée pour permettre le déroulement de l'étape de réticulation avant qu'une quantité suffisante de formaldéhyde quitte le tissu et affecte le procédé.
  4. Procédé selon la revendication 1, dans lequel le tissu en cours de durcissement a une teneur en humidité supérieure à 20 % en poids.
  5. Procédé selon la revendication 2, dans lequel le durcissement à chaud est réalisé à une température de 37,77 °C à 176,66 °C (100 °F à 350 °F).
  6. Procédé selon la revendication 2, dans lequel le durcissement à chaud est effectué dans la plage préférée de 121,11 °C à 162,77 °C (250 °F à 325 °F).
  7. Procédé selon la revendication 1, dans lequel ledit tissu est durci à chaud en augmentant graduellement la température.
  8. Procédé selon la revendication 5, dans lequel le durcissement à chaud est réalisé à une température de 37,77 °C à 148,88 °C (100 °F à 300 °F).
  9. Procédé selon la revendication 1, dans lequel le formaldéhyde se présente sous la forme d'une solution aqueuse de formaldéhyde, ayant une concentration de 0,5 % à 10 %.
  10. Procédé selon la revendication 1, dans lequel la plage préférée de la concentration de formaldéhyde est de 1,5 % à 7 % du poids du tissu.
  11. Procédé selon la revendication 1, dans lequel le tissu est une toile pour chemises 100 % coton.
EP98921043A 1998-05-11 1998-05-12 Procede permettant de rendre un tissu infroissable et sans plis Expired - Lifetime EP1100990B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US09/075,334 US5885303A (en) 1997-05-13 1998-05-11 Durable press/wrinkle-free process
US75334 1998-05-11
PCT/US1998/009367 WO1999058758A1 (fr) 1998-05-11 1998-05-12 Procede permettant de rendre un tissu infroissable et sans plis

Publications (3)

Publication Number Publication Date
EP1100990A1 EP1100990A1 (fr) 2001-05-23
EP1100990A4 EP1100990A4 (fr) 2002-08-07
EP1100990B1 true EP1100990B1 (fr) 2009-07-15

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Application Number Title Priority Date Filing Date
EP98921043A Expired - Lifetime EP1100990B1 (fr) 1998-05-11 1998-05-12 Procede permettant de rendre un tissu infroissable et sans plis

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EP (1) EP1100990B1 (fr)
JP (1) JP4162856B2 (fr)
AU (1) AU7373398A (fr)
CA (1) CA2331646A1 (fr)
DE (1) DE69840983D1 (fr)
ES (1) ES2330978T3 (fr)
WO (1) WO1999058758A1 (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6511928B2 (en) * 1998-09-30 2003-01-28 The Procter & Gamble Company Rayon fabric with substantial shrink-resistant properties
US6375685B2 (en) 1997-05-13 2002-04-23 The Procter & Gamble Company Textile finishing process
US6565612B2 (en) 1998-09-30 2003-05-20 The Procter & Gamble Company Shrink resistant rayon fabrics
US6544296B2 (en) 2000-02-07 2003-04-08 The Proctor & Gamble Company Enhanced fabric comprising substrates and process to provide same
CN1398310A (zh) 2000-02-07 2003-02-19 宝洁公司 增强的含织物的底物及其制造方法
JP4562341B2 (ja) * 2000-02-15 2010-10-13 ストライク、インベストメンツ、リミテッド、ライアビリティ、カンパニー 疎水性漂白剤の使用による織物へのパーマネントプレス加工適用方法
WO2001073185A2 (fr) * 2000-03-29 2001-10-04 The Procter & Gamble Company Procedes servant a ameliorer la brillance de tissus et tissus presentant une brillance amelioree
WO2001073184A2 (fr) * 2000-03-29 2001-10-04 The Procter & Gamble Company Procedes d'amelioration de la capacite d'absorption d'eau des tissus et tissus presentant des proprietes ameliorees
AU2001251127A1 (en) * 2000-03-29 2001-10-08 The Procter And Gamble Company Methods for improving fibrillation or pill resistance of fabrics and fabrics with improved properties

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE438631A (fr) * 1939-04-04
NL286002A (fr) * 1961-11-28
US3420696A (en) * 1964-06-02 1969-01-07 West Point Pepperell Inc Aldehyde fixation on polymeric material
US3812201A (en) * 1972-02-25 1974-05-21 Corning Corp Textile finishing composition and process
US4108598A (en) * 1976-12-02 1978-08-22 The Strike Corporation Durable press process
US4269603A (en) * 1979-05-04 1981-05-26 Riegel Textile Corporation Non-formaldehyde durable press textile treatment
US4369390A (en) * 1981-01-30 1983-01-18 Texas Instruments Incorporated Symmetric beam width compression multistrip coupler

Also Published As

Publication number Publication date
DE69840983D1 (de) 2009-08-27
EP1100990A4 (fr) 2002-08-07
JP4162856B2 (ja) 2008-10-08
EP1100990A1 (fr) 2001-05-23
ES2330978T3 (es) 2009-12-17
JP2003526741A (ja) 2003-09-09
CA2331646A1 (fr) 1999-11-18
AU7373398A (en) 1999-11-29
WO1999058758A1 (fr) 1999-11-18

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