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EP0242495B1 - Stain-resistant nylon carpets - Google Patents

Stain-resistant nylon carpets Download PDF

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Publication number
EP0242495B1
EP0242495B1 EP86870055A EP86870055A EP0242495B1 EP 0242495 B1 EP0242495 B1 EP 0242495B1 EP 86870055 A EP86870055 A EP 86870055A EP 86870055 A EP86870055 A EP 86870055A EP 0242495 B1 EP0242495 B1 EP 0242495B1
Authority
EP
European Patent Office
Prior art keywords
carpet
units
nylon
condensation product
stain
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
EP86870055A
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German (de)
French (fr)
Other versions
EP0242495A1 (en
Inventor
Randolph Compton Blyth
Pompelio Angelo Ucci
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.)
Monsanto Co
Original Assignee
Monsanto Co
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 to US06/768,302 priority Critical patent/US4592940A/en
Application filed by Monsanto Co filed Critical Monsanto Co
Priority to DE8686870055T priority patent/DE3673008D1/en
Priority to EP86870055A priority patent/EP0242495B1/en
Priority claimed from US06/914,507 external-priority patent/US4680212A/en
Publication of EP0242495A1 publication Critical patent/EP0242495A1/en
Priority claimed from US07/370,099 external-priority patent/US4892558A/en
Priority to US07/457,201 priority patent/US5182154A/en
Priority claimed from US07/457,201 external-priority patent/US5182154A/en
Publication of EP0242495B1 publication Critical patent/EP0242495B1/en
Application granted granted Critical
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • D06M15/277Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof containing fluorine
    • 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
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39Aldehyde resins; Ketone resins; Polyacetals
    • D06M15/41Phenol-aldehyde or phenol-ketone resins
    • D06M15/412Phenol-aldehyde or phenol-ketone resins sulfonated
    • 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
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/63Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing sulfur in the main chain, e.g. polysulfones

Definitions

  • nylon carpet means carpet in which the yarn used in making the pile fabric thereof consists essentially of nylon yarn
  • the term “yarn” means a continuous strand of fibers
  • the term “fibers” includes fibers of extreme or indefinite length (i.e. filaments) and fibers of short length (i.e., staple).
  • stain resistant when used herein with reference to carpet means carpet having the ability to resist staining when subjected to Food, Drug and Cosmetic Red Dye No. 40 (herein after referred to as Red Dye 40) under the conditions set forth in the Stain Resistance Test given hereinafter. Briefly, the test involves subjecting a test sample of carpet to two standard washing cycles in a conventional washing machine and then immersing the sample in a solution containing Red Dye No. 40. If the carpet is not visibly stained by the dye under the test conditions, the carpet is stain resistant within the meaning of the term as used herein. The purpose of the test is to identify carpets having durable and lasting resistance to staining normally caused by Red Dye 40.
  • Red Dye No. 40 is an acid dye having the following structure:
  • Nylon carpet is a popular floor covering for both residential and commercial applications. Such carpeting is relatively inexpensive and offers a desirable combination of qualities, such as aesthetics, comfort, safety, warmth and quietness. Also, it is available in a wide variety of attractive colors, patterns and textures. However, nylon carpet is permanently stained by most artificial colourants normally added to foods, berages, medicines, cosmetic, etc., the most common of which is Red Dye No. 40.
  • EP-A 235 989 (not published at the filling date of the present application) describes polyamide fibres made stain-resistant by treating them with a sulphonated naphtolor sulphonated phenol-formaldehyde condensation product.
  • US-A 4 501 591 describes imparting stain resistance to polyamide carpets during a continuous dyeing process, which involves adding to the dye liquor an alkali metal silicate and a sulphonated phenol-formaldehyde condensation product.
  • the present invention provides stain resistanc nylon carpet and a process for obtaining such carpet,
  • the process comprises immersing a carpet having a pile made from nylon yarn in an aqueous solution of a polymeric condensation product consisting essentially of repeating units of the formula where R is the same or different in each unit and is hydrogen or a radical selected from the group consisting of-SOaX, proviso that at least 40% of the total units contain an ⁇ SO ⁇ X radical and at least 40% of the total units contain the linkage, wherein X is H or a cation, e.g.
  • the weigth ratio of aqueous solution to nylon yarn is in the range of 20:1 to 40:1, the pH of the solution is no greater than 4.5, the temperature of the solution is at least 95 ° C and the amount of the condensation product in the solution is sufficient to provide a carpet coated with from 0.1 % to 1.0% of the condensation product based on the weight of nylon yarn.
  • the amount of the polymeric condensation product is preferably from 0.3% to 1.0% based on the weight of nylon fibre. At concentrations above about 1.0% on weight of fibre the fibres become stiff and impart a harsh and undesirable hand to the carpet.
  • carpet treated in accordance with the present invention can be sheared in a conventional manner (i.e., as the last step in the carpet making process) to provide a cut pile carpet in which the freshly exposed pile fibre ends are stain resistant without further treatment. This is important since further treatment of the carpet after the shearing step were required to achieve stain resistance of the exposed ends, such treatment would add significantly to the overall cost of the carpet and, therefore, be undesirable.
  • the aqueous solution should be maintained at a pH no greater than about 4.5 and at a temperature at least about 95 ° C, otherwise, the carpet does not pick up sufficient condensation product to impart stain resistance thereto.
  • the aqueous solution is maintained at a pH of 4.5 at the boil.
  • the ratio of aqueous solution to carpet fibre should be within the range of 20:1 to 40:1. It has been dicovered that in carrying out the process at a ratio of about 20:1 and with the slution at a pH of 4.5 and at the boil, about 40% to 50% of the condensation product is picked up by the immersed carpet in about 30 minutes.
  • the aqueous solution must contain 0.25 to 2.5%, based on the weight of carpet fiber, (a 100 to 150% excess) of the product in order to coat the carpet with a sufficient amount of the product (0.1 to 1.0% on weight of fiber) to impart stain resistance thereto.
  • the exact amount of the excess required in a given instance will depend on the particular processing conditions selected and can be easily determined by routine experimentation.
  • Water-soluble condensation products useful in practicing the process of the present invention may be prepared by the condensation of formaldehyde with one or more phenols selected from the group consisting of (i) diphenolsulfone, (ii) diphenolsulfone sulfonic acid or salt thereof and (iii) phenolsulfonic acid or salt thereof, with the phenols being selected so that at least 40% of the phenols contain the group consisting of (i) diphenolsulfone, (ii) diphenolsulfone sulfonic acid or salt thereof and (iii) phenolsulfonic acid or salt thereof, with the phenols being selected so that at least 40% of the phenols contain the group consisting of (i) diphenolsulfone, (ii) diphenolsulfone sulfonic acid or salt thereof and (iii) phenolsulfonic acid or salt thereof, with the phenols being selected so that at least 40% of the phenols contain the group consisting of (i) diphenolsul
  • sulfonic acid radical or salt thereof contain a sulfonic acid radical or salt thereof.
  • Representative salts of the sulfonic acids include the alkali metal salts, such as sodium and potassium, and the ammonium salt and may be obtained by neutralizing the sulfonic acid with a base such as sodium, potassium or ammonium hydroxide.
  • Condensation products prepared from monosulfonic acids have been found to impart better stain resistance to the carpet than corresponding products prepared from di-or trisulfonic acids and, therefore, are preferred with p-phenolsulfonic acid and 4,4-diphenolsulfone-2-sulfonic acid being particularly preferred.
  • Representative condensation products include the product having repeating units of the formulas where the product ratio of (A) to (B) is 60 to 40 and the product having repeating units of the formulas where the ratio of units (C) to (D) is at least 8:1 and preferable as high as possible with products in which all of units are units (C) being preferred.
  • the molecular weight and the monosulfonate content of the water-soluble condensation product preferably is as high as possible, for example, a molecular weight ranging from 400 to 800 with a monosulfonate content of 100% or as near 100% as possible.
  • the water solubility of the condensation product is influenced by the type of terminal groups present in its structure, for example, hydrophylic groups such as -CH 2 0H and -CH 2 S0 3 H render the product more water soluble than groups, such as methyl groups.
  • the condensation products may conveniently be prepared by methods known in the art, for example, by condensation of the phenols with formaldehyde in an acid or alkaline medium at elevated temperatures.
  • an acid medium from 0.3 to 0.5 mole of formaldehyde is used for each mole of phenol and, in a basic medium, from 0.9 to 1.5 moles of formaldehyde is used for each mole of phenol.
  • the basic condensation provides products having a greater proportion of terminal -CH 2 0H groups and, therefore, greater water-solubility.
  • the nylon carpet is treated during beck dyeing operations, by lowering the pH of the beck dye bath from its normal range of 6.5 to 8.0, to 4.5 or lower.
  • nylon carpets of major commercial importance are those having pile fibers shaped from nylon 66 which is polyhexamethylene adipamide and those shaped from nylon 6 which is polycaprolactam.
  • other nylons from which the pile fibers may be shaped include nylon 11 which is the polymer of 11-amino undecanoic acid, nylon 610 which is polyhexamethylene sebacamide; and copolymers of nylon 66 or nylon 6, for example, a nylon 66/6 copolymer or nylon 66/6TA copolymer where 6TA is hexamethylene terephthalamide.
  • a 5 cm x 5 cm sample of carpet is subjected to two wash cycles in a heavy-duty Sears and Roebuck electric washing machine Model No. 111.7114802.
  • Detergent 100-150 gms
  • ALL@ Lever Brothers Company under the tradename ALL@
  • the settings on the machine are as follows: the fabric setting is Cotton, Linen, Colored; the wash-rinse setting is Warm (48 ° C) Wash/Cold Rinse; the water level setting is Low; and the wash cycle setting is 14 Minute Wash Cycle.
  • washing machine and detergent specified, and equivalent washing machine and/or detergent may be used.
  • the sample is removed from the washing machine and immersed in an aqueous solution of cherry flavoured soft drink premex containing FDC Red Dye No. 40 in which the concentration of the dye is 0.054 gms/liter.
  • the carpet sample is left immersed in the solution for one hour.
  • the sample is then removed from the solution and washed with tap water. If the sample is not visibly stained by the dye, it is characterized as being stain resistant within the meaning of the expression as it is used herein.
  • cut pile tufted carpets were prepared from polyamide fibers and treated in accordance with the process of the present invention.
  • the treated carpets were then tested to evaluate their resistance to staining by various colorants presents in common household substances.
  • a 310 filament, 60 denier (6.7 Tex) per filament (dpf), undrawn nylon 66 yarn was prepared by conventional procedures. Fifty-four (54) such yarns were combined to form a tow having a total denier of about 1,000,000 (111111 Tex). The tow was drawn over rolls to provide nominal 18 dpf tow (20d Tex per filament), crimped in a conventional stuffer box and cut into 7 inch (19.05 cm) staple. The staple was carded, drafted and spun on a conventional ring spinning frame to provide a 2-4cofton count yarn having about 4.5 tpi (177 tpm) of twist in the Z-direction.
  • Two of these yarns were plied on a conventional ring twister to provide a plied yarn having a net twist of 0 tpi in the Z-direction and 3 tpi (118 tpm) in the S-direction.
  • the resulting plied yarn was then heatset.
  • Two cut pile tufted carpets were made from the heatset plied staple yarn and dyed to a light gold color in a conventional beck dyeing operation in which the carpet was immersed in an aqueous dye bath contained within a vessel. The bath was maintained at a pH of 6.5 and at the boiling temperature of the bath (liquor). The weight ratio of liquor to carpet fiber was 20:1.
  • Light gold was selected as being a color which contrasts well with most stains.
  • the liquor was then drained from the dye vessel and replaced with a corresponding amount of water.
  • a water-soluble product formed by the acid condensation of 4,4'-diphenolsulfone, p-phenolsulfonic acid and formaldehyde in which the mole ratio of sulfone to sulfonic acid is about 60:40 was added to the vessel and dissolved in the water in an amount sufficient to provide 0.4% by weight of condensation product on weight of carpet pile fabric.
  • the resulting solution was adjusted to a pH of 4.5 by the addition of an appropriate amount of acetic acid thereto.
  • the solution was then brought to the boil and one of the carpets was immersed (treated) therein for a period of 30 minutes.
  • the treated carpet (invention) and untreated carpet (control) were then sheared (i.e., defuzzed) and used in conducting the following tests.
  • Samples of the treated and untreated (control) carpets were subjected to the common household liquid substances listed in the table below to determine the resistance of the samples to staining by colorants present in these substances. Each substance was applied to the carpet sample, rubbed into the carpet, left on the sample overnight and, finally, the next day the sample was washed to remove the substance, first with a dilute water solution of a commercial detergent and then with water.
  • test B the substance which most severely and permanently stained the untreated carpet samples was the soft drink (cherry flavored) containing Red Dye 40 in a concentration of 0.054 gms/liter.
  • a separate test was conducted to determine the effect of a massive spill of the soft drink on a sample of the treated carpet.
  • one gallon (3785 ml) of the soft drink was poured onto an appropriate sized carpet sample from a gallon milk container, the container being held at a height of one meter above the face of the carpet sample. The soft drink was left on the carpet sample overnight. No steps were taken to clean the carpet or remove any of the soft drink until the next day. The next day the carpet sample was cleaned in the manner described above. Surprisingly, after being cleaned, no visual evidence of the soft drink (Red Dye 40) remained on the carpet sample.
  • Fiber samples taken from the treated and untreated carpets were tested to determine the ability of the fibers to resist staining by the above soft drink.
  • the optical density of a weighed amount of soft drink containing FD&C Red Dye No. 40 was measured on a Carey 15 Spectrophotometer using a cm cell with the light absorption being measured at 520 millimicrons. (Light absorption is a measure of dye concentration of the drink.)
  • the drink was prepared as before according to the instructions on the package containing the premix ingredients.
  • the drink was prepared as before according to the instructions on the package containing the premix ingredients.
  • the light absorption reading was recorded as To.
  • the soft drink was put into a stoppered container with a sufficient amount of fiber sample to provide a weight ratio of drink to fiber of 40:1.
  • the stoppered container of drink and fiber was then shaken on a motorized shaker for a period of two hours.
  • the fiber was then removed from the container and the optical density of the drink was determined as before. The reading this time was recorded as Ti.
  • test results were expressed as a change in light penetration, expressed as a percentage, calculated as follows:

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

Description

    BACKGROUND OF INVENTION 1. Field of the Invention
  • This invention relates to novel stain resistant nylon carpets and to a novel process for providing such carpets. As used herein, the term "nylon carpet" means carpet in which the yarn used in making the pile fabric thereof consists essentially of nylon yarn, the term "yarn" means a continuous strand of fibers and the term "fibers" includes fibers of extreme or indefinite length (i.e. filaments) and fibers of short length (i.e., staple).
  • The term "stain resistant" when used herein with reference to carpet means carpet having the ability to resist staining when subjected to Food, Drug and Cosmetic Red Dye No. 40 (herein after referred to as Red Dye 40) under the conditions set forth in the Stain Resistance Test given hereinafter. Briefly, the test involves subjecting a test sample of carpet to two standard washing cycles in a conventional washing machine and then immersing the sample in a solution containing Red Dye No. 40. If the carpet is not visibly stained by the dye under the test conditions, the carpet is stain resistant within the meaning of the term as used herein. The purpose of the test is to identify carpets having durable and lasting resistance to staining normally caused by Red Dye 40.
  • Red Dye No. 40 is an acid dye having the following structure:
  • Figure imgb0001
  • 2. Description of the Prior Art
  • Nylon carpet is a popular floor covering for both residential and commercial applications. Such carpeting is relatively inexpensive and offers a desirable combination of qualities, such as aesthetics, comfort, safety, warmth and quietness. Also, it is available in a wide variety of attractive colors, patterns and textures. However, nylon carpet is permanently stained by most artificial colourants normally added to foods, berages, medicines, cosmetic, etc., the most common of which is Red Dye No. 40.
  • It is a conventional practice to coat nylon carpet fibres with a fluorochemical to prevent wetting of the carpet surface and thus minimise contact between the carpet surface and foreign substance (e.g. soil). However, such an approach offers very little protection ot the carpet in instances where the foreign substance is a substance such as Red Dye 40 unless, of course, the substance is immediately removed from the carpet before it has a chance to stain the carpet. Survey of the carpet replacement market show that more carpets are replaced due to staining than due to wear. Therefore, there is a need in the art to develop stain resistant nylon carpet having the ability to retain its original appearance for an extended period of time.
  • EP-A 235 989 (not published at the filling date of the present application) describes polyamide fibres made stain-resistant by treating them with a sulphonated naphtolor sulphonated phenol-formaldehyde condensation product.
  • Applying the stain-resist compound at pH values of between 1.5 and 2.5 renders them stable upon exposure to agents in the environment such as N02.
  • US-A 4 501 591 describes imparting stain resistance to polyamide carpets during a continuous dyeing process, which involves adding to the dye liquor an alkali metal silicate and a sulphonated phenol-formaldehyde condensation product.
  • Summary of the invention
  • The present invention provides stain resistanc nylon carpet and a process for obtaining such carpet, The process comprises immersing a carpet having a pile made from nylon yarn in an aqueous solution of a polymeric condensation product consisting essentially of repeating units of the formula
    Figure imgb0002
    where R is the same or different in each unit and is hydrogen or a radical selected from the group consisting of-SOaX,
    Figure imgb0003
    proviso that at least 40% of the total units contain an ~SOεX radical and at least 40% of the total units contain the
    Figure imgb0004
    linkage, wherein X is H or a cation, e.g. NH3, Na, K, etc., and the weigth ratio of aqueous solution to nylon yarn is in the range of 20:1 to 40:1, the pH of the solution is no greater than 4.5, the temperature of the solution is at least 95°C and the amount of the condensation product in the solution is sufficient to provide a carpet coated with from 0.1 % to 1.0% of the condensation product based on the weight of nylon yarn. The amount of the polymeric condensation product is preferably from 0.3% to 1.0% based on the weight of nylon fibre. At concentrations above about 1.0% on weight of fibre the fibres become stiff and impart a harsh and undesirable hand to the carpet.
  • It has been discovered that carpet treated in accordance with the present invention can be sheared in a conventional manner (i.e., as the last step in the carpet making process) to provide a cut pile carpet in which the freshly exposed pile fibre ends are stain resistant without further treatment. This is important since further treatment of the carpet after the shearing step were required to achieve stain resistance of the exposed ends, such treatment would add significantly to the overall cost of the carpet and, therefore, be undesirable.
  • Preferred embodiment of the invention
  • In practising the process of the present invention the aqueous solution should be maintained at a pH no greater than about 4.5 and at a temperature at least about 95°C, otherwise, the carpet does not pick up sufficient condensation product to impart stain resistance thereto. Preferably, the aqueous solution is maintained at a pH of 4.5 at the boil. In order that the condensation product is transferred from the solution to the carpet within a reasonable time, the ratio of aqueous solution to carpet fibre should be within the range of 20:1 to 40:1. It has been dicovered that in carrying out the process at a ratio of about 20:1 and with the slution at a pH of 4.5 and at the boil, about 40% to 50% of the condensation product is picked up by the immersed carpet in about 30 minutes. Accordingly, under these conditions the aqueous solution must contain 0.25 to 2.5%, based on the weight of carpet fiber, (a 100 to 150% excess) of the product in order to coat the carpet with a sufficient amount of the product (0.1 to 1.0% on weight of fiber) to impart stain resistance thereto. Of course, the exact amount of the excess required in a given instance will depend on the particular processing conditions selected and can be easily determined by routine experimentation.
  • Water-soluble condensation products useful in practicing the process of the present invention may be prepared by the condensation of formaldehyde with one or more phenols selected from the group consisting of (i) diphenolsulfone, (ii) diphenolsulfone sulfonic acid or salt thereof and (iii) phenolsulfonic acid or salt thereof, with the phenols being selected so that at least 40% of the phenols contain the
  • Figure imgb0005
    linkage and at least 40% contain a sulfonic acid radical or salt thereof. Representative salts of the sulfonic acids include the alkali metal salts, such as sodium and potassium, and the ammonium salt and may be obtained by neutralizing the sulfonic acid with a base such as sodium, potassium or ammonium hydroxide.
  • Condensation products prepared from monosulfonic acids have been found to impart better stain resistance to the carpet than corresponding products prepared from di-or trisulfonic acids and, therefore, are preferred with p-phenolsulfonic acid and 4,4-diphenolsulfone-2-sulfonic acid being particularly preferred. Representative condensation products include the product having repeating units of the formulas
    Figure imgb0006
    where the product ratio of (A) to (B) is 60 to 40 and the product having repeating units of the formulas
    Figure imgb0007
    where the ratio of units (C) to (D) is at least 8:1 and preferable as high as possible with products in which all of units are units (C) being preferred.
  • The molecular weight and the monosulfonate content of the water-soluble condensation product preferably is as high as possible, for example, a molecular weight ranging from 400 to 800 with a monosulfonate content of 100% or as near 100% as possible.
  • The water solubility of the condensation product is influenced by the type of terminal groups present in its structure, for example, hydrophylic groups such as -CH20H and -CH2S03H render the product more water soluble than groups, such as methyl groups.
  • The condensation products may conveniently be prepared by methods known in the art, for example, by condensation of the phenols with formaldehyde in an acid or alkaline medium at elevated temperatures. In an acid medium, from 0.3 to 0.5 mole of formaldehyde is used for each mole of phenol and, in a basic medium, from 0.9 to 1.5 moles of formaldehyde is used for each mole of phenol. The basic condensation provides products having a greater proportion of terminal -CH20H groups and, therefore, greater water-solubility.
  • According to one aspect of the invention the nylon carpet is treated during beck dyeing operations, by lowering the pH of the beck dye bath from its normal range of 6.5 to 8.0, to 4.5 or lower.
  • Any nylon carpet may be treated in accordance with the process of the present invention. Nylon carpets of major commercial importance are those having pile fibers shaped from nylon 66 which is polyhexamethylene adipamide and those shaped from nylon 6 which is polycaprolactam. other nylons from which the pile fibers may be shaped include nylon 11 which is the polymer of 11-amino undecanoic acid, nylon 610 which is polyhexamethylene sebacamide; and copolymers of nylon 66 or nylon 6, for example, a nylon 66/6 copolymer or nylon 66/6TA copolymer where 6TA is hexamethylene terephthalamide.
  • Stain resistance test
  • The following test procedure is used to identify stain resistant carpet.
  • A 5 cm x 5 cm sample of carpet is subjected to two wash cycles in a heavy-duty Sears and Roebuck electric washing machine Model No. 111.7114802. Detergent (100-150 gms), sold by Lever Brothers Company under the tradename ALL@, is used in both cycles with the second cycle being started immediately after completion of the first cycle. For each cycle the settings on the machine are as follows: the fabric setting is Cotton, Linen, Colored; the wash-rinse setting is Warm (48°C) Wash/Cold Rinse; the water level setting is Low; and the wash cycle setting is 14 Minute Wash Cycle. (If desired, instead of using the washing machine and detergent specified, and equivalent washing machine and/or detergent may be used.) After the second cycle is completed, the sample is removed from the washing machine and immersed in an aqueous solution of cherry flavoured soft drink premex containing FDC Red Dye No. 40 in which the concentration of the dye is 0.054 gms/liter. The carpet sample is left immersed in the solution for one hour. The sample is then removed from the solution and washed with tap water. If the sample is not visibly stained by the dye, it is characterized as being stain resistant within the meaning of the expression as it is used herein.
  • The following example is given to further illustrate the invention.
  • Example
  • In this example cut pile tufted carpets were prepared from polyamide fibers and treated in accordance with the process of the present invention. The treated carpets were then tested to evaluate their resistance to staining by various colorants presents in common household substances.
  • A 310 filament, 60 denier (6.7 Tex) per filament (dpf), undrawn nylon 66 yarn was prepared by conventional procedures. Fifty-four (54) such yarns were combined to form a tow having a total denier of about 1,000,000 (111111 Tex). The tow was drawn over rolls to provide nominal 18 dpf tow (20d Tex per filament), crimped in a conventional stuffer box and cut into 7 inch (19.05 cm) staple. The staple was carded, drafted and spun on a conventional ring spinning frame to provide a 2-4cofton count yarn having about 4.5 tpi (177 tpm) of twist in the Z-direction. Two of these yarns were plied on a conventional ring twister to provide a plied yarn having a net twist of 0 tpi in the Z-direction and 3 tpi (118 tpm) in the S-direction. The resulting plied yarn was then heatset. Two cut pile tufted carpets were made from the heatset plied staple yarn and dyed to a light gold color in a conventional beck dyeing operation in which the carpet was immersed in an aqueous dye bath contained within a vessel. The bath was maintained at a pH of 6.5 and at the boiling temperature of the bath (liquor). The weight ratio of liquor to carpet fiber was 20:1. Light gold was selected as being a color which contrasts well with most stains. The liquor was then drained from the dye vessel and replaced with a corresponding amount of water. A water-soluble product formed by the acid condensation of 4,4'-diphenolsulfone, p-phenolsulfonic acid and formaldehyde in which the mole ratio of sulfone to sulfonic acid is about 60:40 was added to the vessel and dissolved in the water in an amount sufficient to provide 0.4% by weight of condensation product on weight of carpet pile fabric. The resulting solution was adjusted to a pH of 4.5 by the addition of an appropriate amount of acetic acid thereto. The solution was then brought to the boil and one of the carpets was immersed (treated) therein for a period of 30 minutes.
  • The treated carpet (invention) and untreated carpet (control) were then sheared (i.e., defuzzed) and used in conducting the following tests.
  • TEST A
  • Five samples of the treated carpet were subjected to the Stain Resistance Test, described previously herein, except in this instance the washing machine was operated through five wash cycles, detergent being added at the beginning of each cycle. At the completion of each cycle one of the carpet samples was removed from the washing machine. For purposes of comparison a sample of untreated carpet (control) was subjected to Red Dye 40 in accordance with the test. The results of the test are given below.
    Figure imgb0008
  • The results of this test clearly illustrate the stain resistant characteristics of polyamide carpets treated in accordance with the present invention.
  • In a related experiment, a polyamide carpet was treated with the above mentioned water-soluble product in the manner described above except in this instance the pH of the bath was adjusted to 6.5. The treated carpet was then subjected to Test A. The results of the test showed the carpet to be visibly stained after only one wash cycle. This experiment demonstrates the importance of carrying out the treating of the carpet at a low pH.
  • TEST B
  • Samples of the treated and untreated (control) carpets were subjected to the common household liquid substances listed in the table below to determine the resistance of the samples to staining by colorants present in these substances. Each substance was applied to the carpet sample, rubbed into the carpet, left on the sample overnight and, finally, the next day the sample was washed to remove the substance, first with a dilute water solution of a commercial detergent and then with water.
    Figure imgb0009
  • The results in the Table clearly show that carpet treated in accordance with the process of the invention has resistance to staining when compared to the corresponding untreated carpet.
  • TEST C
  • In test B, the substance which most severely and permanently stained the untreated carpet samples was the soft drink (cherry flavored) containing Red Dye 40 in a concentration of 0.054 gms/liter. A separate test was conducted to determine the effect of a massive spill of the soft drink on a sample of the treated carpet. In this test, one gallon (3785 ml) of the soft drink was poured onto an appropriate sized carpet sample from a gallon milk container, the container being held at a height of one meter above the face of the carpet sample. The soft drink was left on the carpet sample overnight. No steps were taken to clean the carpet or remove any of the soft drink until the next day. The next day the carpet sample was cleaned in the manner described above. Surprisingly, after being cleaned, no visual evidence of the soft drink (Red Dye 40) remained on the carpet sample.
  • TEST D
  • Fiber samples taken from the treated and untreated carpets were tested to determine the ability of the fibers to resist staining by the above soft drink. In these experiments, the optical density of a weighed amount of soft drink containing FD&C Red Dye No. 40 was measured on a Carey 15 Spectrophotometer using a cm cell with the light absorption being measured at 520 millimicrons. (Light absorption is a measure of dye concentration of the drink.) The drink was prepared as before according to the instructions on the package containing the premix ingredients. The drink was prepared as before according to the instructions on the package containing the premix ingredients. The light absorption reading was recorded as To. The soft drink was put into a stoppered container with a sufficient amount of fiber sample to provide a weight ratio of drink to fiber of 40:1. The stoppered container of drink and fiber was then shaken on a motorized shaker for a period of two hours. The fiber was then removed from the container and the optical density of the drink was determined as before. The reading this time was recorded as Ti. (If the fiber sample did not resist staining, i.e., took up dye from the drink, the Ti value was less than the To value; on the other hand, if the fiber sample resisted staining, i.e., took up no dye, the To and T1 were the same.) In order to compare samples the test results were expressed as a change in light penetration, expressed as a percentage, calculated as follows:
    Figure imgb0010
  • The lower the percentage, the more resistant the yarn was to staining. In these experiments, fiber samples taken from carpets treated in accordance with the process made of the present invention gave test values ranging from 0 to 1.0%, whereas fibers taken from untreated (control) carpets gave test values ranging from 30 to 35%.

Claims (6)

1. A process for imparting stain resistance to a carpet having apile made from nylon yarn, comprising immersing said carpet in an aqueous solution of a polymeric condensation product consisting essentially of repeating units of the formula
Figure imgb0011
where R is the same or different in each unit and is hydrogen or a radical selected from the group consisting of -S03X,
Figure imgb0012
proviso that at least 40% of the units contain an -SOsX radical and at least 40% of the units contain the
Figure imgb0013
linkage, wherein X is H or a cation and the weight ratio of aqueous solution to nylon yarn is in the range of 20:1 to 40:1, the pH of the solution is no greater than 4.5, the temperature of the solution is at least 95°C and the amount of said condensation product in the solution is sufficient to provide a carpet coated with from 0.1 % to 1.0% of the condensation product based on the weight of nylon yarn.
2. A process of Claim 1, wherein the aqueous solution is maintained at the boil.
3. A process of Claim 1 or Claim 2, wherein said carpet is coated with from 0.3% to 1.0% of the condensation product based on the weight of nylon yarn.
4. A process of any of the preceding claims, wherein R in at least 40% of the units is
Figure imgb0014
and in the remainder of the units is -SO3H or a salt thereof.
5. A process of any of Claims 1 to 3 wherein R in at least 80% of the units is
Figure imgb0015
and in the remainder of the units R is
Figure imgb0016
6. A process of any of the preceding claims, wherein said weight ratio is about 20:1.
EP86870055A 1983-12-16 1986-04-25 Stain-resistant nylon carpets Expired - Lifetime EP0242495B1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US06/768,302 US4592940A (en) 1983-12-16 1985-08-22 Stain-resistant nylon carpets impregnated with condensation product of formaldehyde with mixture of diphenolsulfone and phenolsulfonic acid
DE8686870055T DE3673008D1 (en) 1983-12-16 1986-04-25 Stain-resistant NYLON CARPETS.
EP86870055A EP0242495B1 (en) 1983-12-16 1986-04-25 Stain-resistant nylon carpets
US07/457,201 US5182154A (en) 1983-12-16 1989-12-26 Stain resistant nylon carpets

Applications Claiming Priority (10)

Application Number Priority Date Filing Date Title
US56237083A 1983-12-16 1983-12-16
US64360684A 1984-08-23 1984-08-23
US83480486A 1986-03-06 1986-03-06
EP86870055A EP0242495B1 (en) 1983-12-16 1986-04-25 Stain-resistant nylon carpets
US06/914,507 US4680212A (en) 1986-03-06 1986-10-02 Stain resistant nylon fibers
US5971487A 1987-06-08 1987-06-08
US8477787A 1987-08-13 1987-08-13
US29630189A 1989-01-09 1989-01-09
US07/370,099 US4892558A (en) 1986-03-06 1989-06-21 Process for dyeing stain resistant nylon carpets
US07/457,201 US5182154A (en) 1983-12-16 1989-12-26 Stain resistant nylon carpets

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EP0242495A1 EP0242495A1 (en) 1987-10-28
EP0242495B1 true EP0242495B1 (en) 1990-07-25

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Publication number Priority date Publication date Assignee Title
WO1989007168A1 (en) * 1988-02-01 1989-08-10 Allied-Signal Inc. Application of stain blockers to installed carpet
JPH04240271A (en) * 1990-07-14 1992-08-27 Hoechst Ag Method for soilproofing treatment of nylon or woolen fiber material
DE4223830A1 (en) * 1992-07-20 1994-01-27 Sandoz Ag Dirt-repellent finishing agent

Citations (1)

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Publication number Priority date Publication date Assignee Title
EP0235989A1 (en) * 1986-02-14 1987-09-09 E.I. Du Pont De Nemours And Company Method for producing stain resistant polyamide fibers

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Publication number Priority date Publication date Assignee Title
FR1062949A (en) * 1952-09-13 1954-04-28 Composition for cleaning and regenerating superpolyamide yarns
CH464141A (en) * 1966-06-03 1968-07-15 Ciba Geigy Process for printing textile material made of synthetic polyamide fibers
US4501591A (en) * 1983-12-27 1985-02-26 Monsanto Company Process for conveniently providing stain-resistant polyamide carpets

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0235989A1 (en) * 1986-02-14 1987-09-09 E.I. Du Pont De Nemours And Company Method for producing stain resistant polyamide fibers

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