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Publication numberUS2480775 A
Publication typeGrant
Publication date30 Aug 1949
Filing date3 Jul 1948
Priority date3 Jul 1948
Publication numberUS 2480775 A, US 2480775A, US-A-2480775, US2480775 A, US2480775A
InventorsLawrence F Ryan
Original AssigneeDu Pont
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Dyeing nylon hosiery
US 2480775 A
Abstract  available in
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Claims  available in
Description  (OCR text may contain errors)

Patented Aug. 30, 1949 DYEING NYLONIHOSIERY Lawrence F. Ryan, Carneys Point,-N. J., assignor to E. I. du Pont de Nemours & Company, Wilmington, Del., a corporation of Delaware N Drawing. Application July s, 1948,

Serial No. 37,001 I j 2 Claims. (01., s- -55) This invention relates to the dyeing of nylon, and more particularly to an improvement in the process of dyeing nylon hosiery in which mono: filament and multifilament yarns of difierent denier are employed in their fabrication, such as in the manufacture of sheer nylon hosiery for ladies wear.

The term "nylon is used in this specification to designate the new synthetic, fiber-forming, linear polyamides generally referred to in the trade today as nylonand which are described in the patents of W. H. Carothers U. S. 2,071,250, 2,071,253, 2,130,523, 2,130,948, 2,174,527 and 2,195,166. The nylon to which the present invention relates more particularly is that synthetic, fiber-forming linear polyamide produced by the condensation of adipic acid and hexamethylene diamine, as described in the abovementioned patents.

The dyeing of nylon fibers with the various types of dyes was early considered in a paper by P. H. StOtt, published in American Dyestuif Reporter, vol. 28, No. 20, October 2, 1939. Up' to the present time it has been found that the acetate rayon colors, which are water-insoluble, dispersed dyes give the most satisfactory results in the dyeing of nylon fibers, particularly in the dyeing of nylon hosiery. Under ordinary conditions in the dyeing ofnylon multifilament yarns of varying denier, the same or closely similar tones are obtained as distinguished from the different shades or tones which are obtained when nylon yarn of varying denier is dyed with other types of dyes.

More recently, however, there has been intro duced in the hosiery trade new types of sheer nylon hosiery for ladies wear which are constructed of from to denier monofilament yarn in the leg or boot and of to 60 denier plied nylon multifilament yarn in the welt. In the initial attempts to dye this new type of hosiery the acetate colors were used, for experience over a number of years has shown that this type of dyestuff gives far superior results in the dyeing of nylon than any other type of dye. These waterinsoluble-cellulose acetate dispersed colors have been found to give good dye union at junctions etween nylon fibers having slightly different.

physical or chemical properties, such as draw ratio, acidic or basic end groups, etc., as well as junctions of nylon multifilament yarns of somewhat difierent deniers. I

It was found, however, that this type of dye, when employed on hose made from 10 to '20 denier monofilament in the leg and from 30 to 60 denier multifilament in the welt, did not give a satisfactory union. Various expedients were tried to improve theunion, such as by increasing the dyeing time or by increasing the dyeing temperature, but these expedients did not give the necessary improvement, or, if some improvement was obtained, other difliculties were experienced such as creasing of the hosiery, etc. The hosiery dyed with the acetate dispersed colors had more color in the leg of the hose than in the welt, and this elfect detracted from the salability of the product because of the-psychological block apparently set up in the minds of those persons who had not accepted'hosiery dyed in contrasting strength in their various portions. It was, therefore, necessary to find some method for dyeing such hosiery with a good color union between the monofilament and the multifilament of varying deniers.

'It is therefore an object of this invention to provide a process for dyeing nylon hosiery composed in part of monofilament and in part of multifilament, which filaments are of different denier, in substantially the same shade by a simple andeconomical procedure and one that can be satisfactorily employed in the dyeing of this fiber without producing other undesirable effects, A more specific object of this invention is to dye nylon hose, .constructed of from 10 to 20 denier nylon monofilaments in the leg and of 30to denier nylon multifilaments in the welt, with cellulose acetate colors by a method which will give goodcolor union between the welt and the leg.

I have found that nylon hosiery constructed of monofilaments and multifilaments of varying denier can be dyed with dispersed cellulose acetate dyes in much more uniform shades where the dyeing is carried out in the presence of from 2% to 10% of tannicacid, based on the weight of the nylon being dyed. The dyeing, in the presence of the tannic, acid ispreferably carried out in the presence of a weak organic acid, such as acetic acid or formic acid, although the use of the auxiliary acid may be omitted, where desired. Wetting and dispersing agents, such as the higher fatty alcohol sulfates, may also be employed in treating the nylon material with the tannic acid solution. In carrying out the dye process; the hose are preferably scoured in the usual manner, rinsed free from the scouring assistants and then treated at temperatures of from to F. with a solution of tannic acid and acetic acid, with or without the addition in that solution of a higher fatty alcohol sulfate. The

fiber so treated may then be dyed in the usual" manner with the cellulose acetate dyes at the temperatures ordinarily employed. Where it is found to be desired, the dispersed cellulose acetate dyes may be added directly to the tannic acid treating bath after the textile has been thoroughly wetted with the acid solution.

The tannic acid-acetic acidcombination has been found-to give best results when used 'to pretreat the hose before dyeing. However, improved results can be obtained when the tannic acid acetic acid combination is added simultaneously with the acetate color at the start of the'dyeing operation. In general, the-dyeing of the "nylon with the cellulose acetate oolorsisparried out under conditions normally used mnyeing nylon with this type of dye. The preferred temperature for the dye operation is within the range of 155 to 165 F., for below 155 F. the dye absorption is too slow and above 165 F. the tendency toward the formation of creases in the nylon hose g is increased sothat highertemperaturesare preferably avoided. Thetime' required in carrying out the'dyeing process is'substantially that'employed in conventional nylon" hosiery dyeing The following examples are given to illustrate theinvention. The partsused are by weight, unless'otherwise specified. Where percentages are employed, they arebasedon the weight of the nylon being treated, unless otherwise designated.

Example 1.-'-'A lb.'capacity drum rotary dyeing -1iiachine was charged with 19 gallons parts based on the weight of the -hose) of softened'waterand 4' lbs: (dryweight) of scoured and rinsed womens" nylon hosiery with a 15 denier 'xn'onofi'lament b'ootand'a40 denier multifllament twisted welt. There was added 0.193 lb. of tannic 'acidand 0.11 lb; 'of acetic acid (28% strength) with continuous'agtltationof the hose at 90 l. The temperaturewas raised to 125 130 F. and agitation continued for 15 minutes. Thereafter; a" mixture of th'efollowing acetate rayon colors, which hadheen'previously dispersed in water-with 0.05 lb "of along chain aliphatic alcohol sulfate (such as prepared'from 'com mercial alcohols of from 10"to"18' carbonatonrs, s'uch'as cetyl'j'lauryl,"oleyl; .etc;', and which will bereferred' to' hereinafter generally as Du p'onol); was added. 'The'colors'usedin this'ex ainple are dye powders prepared in' readily' disp'ersible form suitable for the dyeing-of cellulose acetate rayon and-which containtherusuai dispersing agents.

0.0252 lb.--Yellow azo dye, containing 40% color solids, which dye was prepared front r-piloteaniline and" p chlorophenol' according to the process of Example Iof'U. SQP. 2,366,034 0.0198 IbL- Acetamine scarlet 3 (containing 30% color-solids)(prototype 100.244) 0.0170lb.-'+Celanthrene brilliant blue FFS, con- 'taining 36% colq'r's'olids (prototyp'eNo.'-228)" The temperature was raised to 160 F. and held for two hours wan the dyeing proceeded. The dye bath was then drained and the hose given a rinse, followed by drying in the normal manner. Bythis method the hose was 'dye d a shade similar to the Bronze'skin shade given in 1947 Fall Season Hosiery Color'C ard of America. An excellent'color balance between the'boot and the welt resulted. This balance was much superior to that obtained when the hose was dye'd'with theabove dye formula by theusual hosiery dyeing. method in which the acetate colors are'ap' Pounds .fDuponol, 0.48 Soap 1.9 ir sod umiphosp at The scour .bath was dropped and the hose rinsed We wi h wat r TTher'e was then charged into the rotary dyeing machine, at F.:

softened water gallons 200 Tannic acid pounds 4.0 Acetic acid (56%) do 3.0 Duponol do' 075 The temperature was raised to -l 30 I. and heldfor 15 m nutes.

The same colors employed in Example 1, and which were dispersed in water with 0.25 lbl of 191229 9 w e addem 0.171 1b.--Yellow azo dye (40% color solids) 0.171 'lb.-Acetamine scar1et'B"(30%color solids) 0.235 'lb.'-Celanthrene brilliant blue FFS (36% "ch1or"so1ids) 1' The temperature was raised to F. and the dyeing'run for one hour at this temperature.

T b t was dr ed. he o e We'll rinsed with'wa'ter. andfinally dried. By the above process, a Mistique shade (1947 Fall Season Hosiery 'Color Card'of America) was obtained with an excellent color unionbetween the boot and the welt.

"To'demonstrate the wash fastness of the nylon hosiery 'dyed'by the above'ijnethod a series of twenty-five wash tests, with drying of thehose between each test, was run. .The wash tests were run tor "one-half hour each at 105 F. with a 30:1 yolu'rne (based on the'weight of the hose) or a 0.5% Soap solution. The averageloss in tinotorial'st fength'over the entire'ser'ies of tests was about 20% in the 'boot and 40% m the welt. Hence. the tannic acid method of dyeing yields improved color balance or uniformity between the yen and the leg; and at the same time the hostess dyed have'wash'fastnes's equal or superior to that dyed by conventional methods.

Eromple 3.-A 15 lb. drumrotary dyeing maehi'newas charged with:' Soft water gallons 18 Womens'nylon hose as described in Ex. 1

pounds 1.5

With agitation, there was added:

Pounds Tannie acid 0.157 Acetic acid (56% 0.110

The temperature was raised to l25-130 E. and a tat on continued f s minutes. Thereafter; adi r s n Qs" i Pounds Tannic acid 0.3 Formic acid (87%) 0.15 Zinc chloride 0.15

in about 30 gallons of soft water, by warming from 80-90 F. to 160 F. and holding with continual agitation at 160 F. for one-quarter hour. The bath was then discharged and the rotary dyeing machine was partially filled with cold water again and agitated while adding:

0.24 lb. trisodium phosphate and the following colors:

0.0193 lb.-Yellow azo dye used in Ex. 1 (40% color solids) 0.0186 lb.Acetamine scarlet B (30% color solids) 0.0265 lb.-Celanthrene brilliant blue FFS (36% color solids) dispersed in one gallon of warm water containing:

Pounds Soap 0.06 Duponol 0.015

The temperature was gradually raised over 15 minutes to 160 F. and held for three-quarters of an hour. The hose were dyed a dark brown shade with good union between the leg and the welt.

For light hosiery shades, it is recommended that a combination of 5% of tannic acid and 3% of acetic acid (28% strength) be used. For dark hosiery shades, of tannic acid and 5% of acetic acid (28% strength) has been found suitable. For very light shades, as little as 2% of tannic acid will be sufi'icient, and even less acetic acid. As stated above, when desired the acetic acid may be omitted, but in general it is found advantageous to use at least small amounts. The percentage figures represent the percentage based on the dry weight of the hose.

The tannic acid in which the nylon hosiery is to be treated may be of any desired volume, preferably from 20 to 40 parts of water per part of nylon to be treated, which volumes are similar to those normally employed in the dyeing of the nylon with water insoluble dispersed cellulose acetate dyes.

While Duponol has been employed in illustrating the invention, any detergent, wetting and dispersing agent (preferably one that is insensitive to calcareous water) which operates in acid solutions, may be employed. The present invention is not dependent upon any specific detergent or wetting agent.

I claim:

1. A process of dyeing nylon hosiery composed in part of monofilament and in part of multifilament yarns of different denier with water insoluble dispersed cellulose acetate dyes, which comprises treating the nylon in an aqueous bath containing from 5% to 10% of tannic acid and from 3% to 5% of an acid of the group consisting of acetic and formic acids, both percentages being based on the weight of the nylon, and applying the water insoluble dispersed dyes by heating the nylon in the aqueous dispersion thereof.

2. A process of dyeing nylon hosiery composed in part of monofilament and in part of multifilament yarns of different denier with water insoluble dispersed cellulose acetate dyes, which comprises treating the nylon in an aqueous bath containing from 5% to 10% of tannic acid based on the weight of the nylon, and thereafter applying to the nylon containing the tannic acid the water insoluble dispersed dyes by heating the nylon in the aqueous dispersion of the dye.


REFERENCES CITED The following references are of record in the file of this patent:

Nylon Dyeing, by Clapham, article in American Dyestuff Reporter for May 3, 1948, pages P299, P300. I

Non-Patent Citations
1 *None
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US2921945 *17 May 195419 Jan 1960Celanese CorpYellow diphenylamine dyes
US2938762 *15 Nov 195531 May 1960American Cyanamid CoDiazotization in presence of developer
US3012842 *12 Nov 195712 Dec 1961Sandoz AgProcess for the level dyeing of textile materials composed of polyamide fibers which possess irregular affinity for dyestuffs
US3060550 *27 Mar 195930 Oct 1962American Enka CorpTreatment of polyamides
US3118723 *8 Feb 196121 Jan 1964Arthur J I HardingProcess for dyeing nylon to produce multi-colored dyeings
US3179483 *14 Feb 196220 Apr 1965American Cyanamid CoMixtures of cationic and non-ionic surfactants, chlorinated triphenylmethanes and tanning agents and union dyeing therewith
US3467484 *7 Mar 196616 Sep 1969Martin Processing Co IncPatterned application of benzyl alcohol with or without a resist on nylon fabrics and dyeing the patterned fabric
US6024770 *28 Sep 199415 Feb 2000N.V. Denderland-MartinProcess to improve resistance to stains on yarns and derived products
US6507980 *21 Aug 200121 Jan 2003Abus August Bremicker Sohne KgHolder
US72760858 Dec 20042 Oct 2007Shaw Industries Group, Inc.Methods of treating and cleaning fibers, carpet yarns and carpets
US748835121 Aug 200710 Feb 2009Columbia Insurance CompanyMethods of treating and cleaning fibers, carpet yarns and carpets
US778537424 Jan 200531 Aug 2010Columbia Insurance Co.Methods and compositions for imparting stain resistance to nylon materials
US20050015886 *24 Jul 200327 Jan 2005Shaw Industries Group, Inc.Methods of treating and cleaning fibers, carpet yarns and carpets
US20080047077 *21 Aug 200728 Feb 2008Jones Dennis J JrMethods of treating and cleaning fibers, carpet yarns and carpets
DE958466C *29 Nov 195121 Feb 1957RhodiacetaVerfahren zum Faerben von Textilien aus Acetylcellulose oder aus vollsynthetischen Faeden
DE1032211B *7 May 195219 Jun 1958Raduner & Co AgVerfahren zum Faerben von Polyamidfasermaterial
U.S. Classification8/531, 8/483, 8/596, 8/924, 8/DIG.210, 8/908, 8/931
International ClassificationD06P3/24, D06P3/26, D06P1/653
Cooperative ClassificationD06P3/26, Y10S8/21, D06P1/6536, Y10S8/931, D06P3/854, Y10S8/924, Y10S8/908
European ClassificationD06P1/653D, D06P3/26, D06P3/854