BACKGROUND OF INVENTION
1. Field of the Invention
[0001] 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).
[0002] 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.
[0003] Red Dye No. 40 is an acid dye having the following structure:
[0004]

2. Description of the Prior Art
[0005] 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.
[0006] 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.
[0007] 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.
[0008] 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 N0
2.
[0009] 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
[0010] 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
~SOεX radical and at least 40% of the total units contain the

linkage, wherein X is H or a cation, e.g. NH
3, 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.
[0011] 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
[0012] 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.
[0013] 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
[0014]

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.
[0015] 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.
[0016] 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.
[0017] 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
20H and -CH
2S0
3H render the product more water soluble than groups, such as methyl groups.
[0018] 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 -CH
20H groups and, therefore, greater water-solubility.
[0019] 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.
[0020] 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
[0021] The following test procedure is used to identify stain resistant carpet.
[0022] 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.
[0023] The following example is given to further illustrate the invention.
Example
[0024] 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.
[0025] 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.
[0026] The treated carpet (invention) and untreated carpet (control) were then sheared (i.e.,
defuzzed) and used in conducting the following tests.
TEST A
[0027] 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.

[0028] The results of this test clearly illustrate the stain resistant characteristics of
polyamide carpets treated in accordance with the present invention.
[0029] 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
[0030] 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.

[0031] 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
[0032] 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
[0033] 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 T
i 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 T
1 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:

[0034] 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%.
1. Verfahren zur Erzeugung von Fleckenunempfindlichkeit bei einem Teppich mit einem
aus Nylongarn hergestellten Flor, dadurch gekennzeichnet, daß man den Teppich in eine
wäßrige Lösung aus einem Polymerkondensationsprodukt aus im wesentlichen sich wiederholenden
Einheiten der Formel

worin R gleich oder verschieden in jeder Einheit ein Wasserstoffatom oder eine Gruppe
der Gruppe mit den Formeln -S0
3X,

mit der Maßgabe bedeutet, daß mindestens 40% der Einheiten eine Gruppe der Formel
-S0
3X und mindestens 40% der Einheiten die Verknüpfung der Formel

enthalten, worin X ein H-Atom oder ein Kation bedeuten, eintaucht und das Gewichtsverhältnis
von wäßriger Lösung zu Nylongarn im Bereich von 20:1 bis 40:1 liegt, der pH-Wert der
Lösung nicht größer als 4,5 ist, die Temperatur der Lösung mindestens 95
°C beträgt und die Menge des Kondensationsprodukts in der Lösung zur Herstellung eines
mit 0,1 bis 1,0% des Kondensationsprodukts, bezogen auf das Gewicht des Nylongarns,
beschichteten Teppichs ausreicht.
2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß man die wäßrige Lösung auf
dem Siedepunkt hält.
3. Verfahren nach Anspruch 1 oder Anspruch 2, dadurch gekennzeichnet, daß man den
Teppich mit 0,3 bis 1,0% des Kondensationsprodukts, bezogen auf das Gewicht des Nylongarns,
beschichtet.
4. Verfahren nach einem der vorangegangenen Ansprüche, dadurch gekennzeichnet, daß
R in mindestens 40% der Einheiten als Gruppe der Formel

vorliegt und in den restlichen Einheiten als Gruppe der Formel -SOsH oder Salz davon
vorliegt.
5. Verfahren nach einem der Ansprüche 1 bis 3, dadurch gekennzeichnet, daß R in mindestens
80% der Einheiten als Gruppe der Formel

vorliegt und in den restlichen Einheiten R als Gruppe der Formel

voliegt.
6. Verfahren nach einem der vorangegangenen Ansprüche, dadurch gekennzeichent, daß
das Gewichtsverhältnis 20:1 beträgt.
1. Procédé pour communiquer une résistance au tâchage à un tapis dont le poil est
constitué d'un fil de nylon, comprent l'immersion de ce tapis dans une solution aqueuse
d'un produit de condensation polymère essentiellement constitué de motifs répondant
à la formule:

dans laquelle R est identique ou différent dans chaque motif et est un atome d'hydrogène
ou un radical choisi dans le groupe constitué de -SO
3X,

sous réserve qu'au moins 40% des motifs contiennent un radical -S0
3X et qu'au moins 40% des motifs contiennent la

dans laquelle X est H ou un cation, et le rapport pondéral de la solution aqueuse
au fil de nylon est dans l'intervalle de 20 : 1 à 40 : 1, que le pH de la solution
n'est pas supérieur à 4,5, que la température de la solution est d'au moins 95°C et
que la quantité de ce produit de condensation dans la solution est suffisante pour
donner un tapis revêtu de 0,1% à 1,0% du produit de condensation par rapport au poids
du fil de nylon.
2. Procédé selon la revendication 1, dans lequel la solution aqueuse est maintenue
à l'ébullition.
3. Procédé selon les revendications 1 ou 2, dans lequel ce tapis est revêtu de 0,3%
à 1,0% du produit de condensation par rapport au poids du fil de nylon.
4. Procédé selon l'une quelconque des revendications précédentes, dans lequel R, dans
au moins 40% des motifs, est

et dans les autres motifs, -SO
sH ou un de ses sels.
5. Procédé selon l'une quelconque des revendications 1 à 3, dans lequel R, dans au
moins 80% des motifs, est:

et dans les autres motifs R est
6. Procédé selon l'une quelconque des revendications précédentes, dans lequel ce rapport
pondéral est de 20 : 1.