AU6413200A - Method and composition for whitening textiles - Google Patents

Description

AUSTRALIA

PATENTS ACT 1990 COMPLETE SPECIFICATION NAME OF APPLICANT(S): Rohm and Haas Company ADDRESS FOR SERVICE: DAVIES COLLISON CAVE Patent Attorneys 1 Little Collins Street, Melbourne, 3000.

INVENTION TITLE: Method and composition for whitening textiles The following statement is a full description of this invention, including the best method of performing it known to me/us:- BACKGROUND OF THE INVENTION The present invention relates to a method and composition for whitening textiles. In particular, the present invention relates to a method and composition for whitening textiles where oxidative bleaching is not desirable.

Wet processing of fabrics is a multi-step process, generally including at least: scouring, bleaching and finishing. Where the fabric is a stretch or elastomeric fabric, the process also typically involves heat-setting prior to wet-processing. Selection of 10 the steps in processing a particular fabric depends upon several factors, including desired appearance and performance of the finished fabric.

Bleaching is a typical part of the wet-processing because traditional fabrics made with natural fibers are typically buff or off-white in color, not "blue-white" that is, white without a yellow cast. On the other hand, synthetic fibers developed 15 over the recent decades are typically white, either because the material itself is white, or because whitener is added to the fiber; however, during processing of fabric made from such fibers, yellowing may occur. This yellowing occurs during heat setting, a high temperature process wherein various properties such as resiliency, elasticity and wrinkle-resistance are imparted to the fabric. When yellowing occurs, such 20 fabrics may also be subjected to reductive bleaching.

For the majority of fabrics, bleaching is typically accomplished with strong oxidizing agents such as: hydrogen peroxide and other peroxide generators, or chlorine-containing bleaches including sodium hypochlorite, calcium hypochlorite or sodium chlorite. With certain fabrics, however, it is not desirable to use such strong bleaching agents, as such agents could degrade the fabric.

Where fabrics are not suitable to bleaching with an oxidizing agent, a reducing scour or reducing bleach (collectively, "reducing bath") can be used. The reducing agent in such reducing baths is generally sodium dithionite (usually referred to as sodium hydrosulfite or hydro) or thioureadioxide (also known as formamidinesulfinic acid or FAS). Sodium hydrosulfite is very unstable, especially DN 99-076 -2when it comes into contact with even small amounts of water, and often spontaneously combusts. Sodium hydrosulfite is typically provided as a powder containing 70-90 wt active hydro, sodium carbonate as a fire retardant, and a chelating or sequestering agent such as EDTA or STPP. Hydro is also now available as an aqueous solution; however, such solutions are prone to oxidation and must be stored under an inert atmosphere (and refrigerated for longer term storage).

Although hydro is widely used in the textile industry, there are severe limitations to the use of this reducing agent. The most severe limitations include: the high fail rate, even with multiple passes through the reducing bath; the low amount of S 10 resultant whitening; the strong sulfur smell (caused by emission of SO 2 and the high flammability of hydro powder.

oooo°: A typical conventional reducing bath contains sodium hydrosulfite, defoamer and wetting agents. Other chemicals useful in the reducing bath include, without limitation: other surfactants, sequestrants, caustic (usually soda ash or NaOH) and optical brighteners. The amount and type of chemicals used in the reducing baths will depend on the fabric being treated, method of treatment and end use of goods.

In general, about 3% hydro is added to the reducing bath at the beginning of the process, and then a second dose of about 3% is added about halfway through the treatment (over about 10 min), so that the typical residence time of fabric in a see.

20 conventional reducing bath is about I 1.5 hrs. Wet-processing of grey fabric

S

usually takes about 6-9 hrs, and multiple treatments may be used. Sometimes the reducing bath step is repeated in order to increase whitening. This can occur immediately after the first reducing bath step, or the whole wet-processing procedure can be repeated. Even after such treatments, the differences in whitening between the treated and untreated fabric will not be readily discernible to the naked eye, and can only be determined by spectral analysis.

There is therefore a need for a reducing bleach for fabrics which is safe, easy to use, cost-effective, and highly efficacious. As detailed below, the present invention accomplishes all of these objectives.

DN 99-076 -3- STATEMENT OF THE INVENTION The present invention is directed to a system for bleaching fabric comprising greige fabric to be treated, a two component reducing solution, and means for heating said reducing solution to 70 to 110 OC; wherein said first component of the reducing solution comprises between 0.1 and 0.6 owg borohydride and said second component of the reducing solution comprises bisulfite in water said bisulfite being present in a stoichiometric excess relative to the borohydride, and wherein the first component of the reducing solution is added to the second component just prior to treatment of the greige fabric.

10 The present invention is also directed to a method for bleaching greige fabric, comprising the steps of contacting greige fabric with a two-part reducing solution for a time sufficient to cause bleaching of the greige fabric to occur, wherein: such o. two-part reducing solution comprises a first component comprising between 0.1 and 0.6 owg borohydride and a second component comprising bisulfite in water, said 15 bisulfite being present in a stoichiometric excess relative to the borohydride; and the first component of the reducing solution is added to the second component just prior to contacting the greige fabric with the reducing solution; and the two part reducing solution is maintained at a temperature between 70 and 110 °C during bleaching of the greige fabric.

20 DETAILED DESCRIPTION OF THE INVENTION As used in this specification, the following terms have the following definitions, unless the context clearly indicates otherwise. "Greige" or "grey" fabrics are those just off the loom or knitting machine and which have only been partially finished not yet dyed). "Fabric" or "textile" means, without limitation, yarns in skein or package form, and all woven, non-woven or knitted goods made from spun fibers, filamentary fibers or yarn and selected from natural and synthetic materials.

Such natural and synthetic materials include but are not limited to: cellulosic acetates such as cellulose acetate and cellulose triacetate; silk, wool, and other protein fibers, flax and other bast fibers; nylon and other polyamide fibers; elastomeric or rubber fibers; acrylics; polyethylene terephthalate; and cotton and DN 99-076 -4rayon fibers. "Spandex" fibers are elastomeric fibers in which the fiber forming substance is a long-chain synthetic polymer of at least 85% of a segmented polyurethane, and generically included both polyether- and polyester-segmented polyurethanes. "Yarn" means a continuous strand of fibers, filaments or other material in a form suitable for knitting weaving or otherwise intertwining to form a textile fabric. "Elastomeric" fibers or yarn are those which at room temperature can be stretched repeatedly to at least twice their original length, and which, upon immediate release of the stretch, will return with force to approximately the original length. "Elastomeric fabrics" are fabrics comprising some elastomeric yarn in either 10 the warp or weft (filling) orientation of the fabric. The following abbreviations are S used throughout the specification: min minutes; hr hours; owg percent of the textile weight (on the weight of the goods) owb percent on weight of bath; wt percent by weight; g grams; L liters; g/L grams per liter. Unless otherwise specified, temperatures are in degrees centigrade and ranges 15 specified are to be read as inclusive.

The reducing bleach solution of the present invention is a two-component solution, typically aqueous. The first component contains a borohydride, and the second component contains a bisulfite in aqueous medium. The first component is added to the second component just prior to fabric treatment. In general, the 20 reducing bath will also contain defoamer and wetting agent, usually added to the second component. Other chemicals useful in the reducing bath include, without limitation: other surfactants, sequestrants, caustic (usually soda ash) and optical brighteners. Such ingredients and their amounts are known to those skilled in the textile arts.

Borohydride and bisulfite react in water (at about pH 5-8) to produce hydrosulfite in situ according to the following equation 1:

BH

4 8 HSO 3 H 4 S204- 2

B(OH)

3 5 H 2 0 (Eq. 1) In addition, it has been suggested that the radical anion .S02-, also a strong reducing agent, is a possible intermediate in this reaction. See, for example, Cook, M. M. in Environmental Chemistry of Dyes and Pigments, pp 33-41 (Reife et al., ed; J. Wiley, DN 99-076 1996). Although the exact mechanism of this reaction has not been fully characterized and this invention is in no way limited by any particular theory or mechanism of action, it is believed that this radical anion also contributes to the reducing ability of the reducing bleach of the present invention.

The amount of borohydride useful in the system of the present invention is between 0.1 and 0.6 owg, preferably between 0.1 and 0.5 owg, and most preferably between 0.1 and 0.3 owg. Any borohydride may be used so long as the counterion does not interfere with fabric wet-processing. It is preferred to use a borohydride of formula T(BH 4 wherein T is an alkaline metal, alkali earth metal or 10 ammonium, and y is 1 or 2, depending on the valence of T. It is particularly preferred to use sodium or potassium borohydride. Borohydride is readily available o as an aqueous alkaline solution containing 12 wt sodium borohydride and wt sodium hydroxide. Such aqueous solution is available as COLORSTRIPT m 2000 from Rohm and Haas Company Andover, MA). If such an aqueous borohydride solution is used, the amount suitable for purposes of the present invention is between 10 to 30 wt preferably no more than about 25 wt of the amount of active anhydrous hydrosulfite recommended for conventional reducing bleaches, which will depend on the fabric to be treated.

The amount of bisulfite used in the present invention will depend in part on 20 the amount of borohydride. As shown above in Eq. 1, 8 moles of bisulfite are required for each mole of borohydride; however, it is desired to use a stoichiometric excess, particularly a molar excess of at least 10 In general, the bisulfite will be of formula M(HSO 3 wherein M is an alkaline metal, alkali earth metal or ammonium, and x is 1 or 2, depending on the valence of M. It is preferred to use sodium or potassium bisulfite. Where the borohydride is used in the form of an aqueous alkaline solution, a greater amount of bisulfite is needed. For example, such a borohydride solution containing 40 wt caustic such as sodium hydroxide requires an additional 3.2 mole of bisulfite; thus in this case it is preferable to use up to about 12 moles of bisulfite per mole of borohydride. If the borohydride solution includes caustic, up to 40 wt of caustic can be used. Such caustic is generally selected from DN 99-076 -6- Q(OH)z, wherein Q is an alkaline metal, alkali earth metal or ammonium, and z is 1 or 2, depending on the valence of Q. It is preferred to use sodium hydroxide.

A typical wet-processing of elastomeric fabric using the system of the present invention includes the steps of: scouring, reducing bleach, whitening (optical brightening), dyeing, and acid washes. A typical amount and type of fabric used in such processing is as follows: Weight of Goods 275 kg of 80% nylon/20% Lycra® warp knit fabric.

The initial step consists of contacting the fabric with a scouring bath (scouring agent and wetting agent) for about 1 to 2.5 hrs.

The second step consists of contacting the fabric with the reducing bath such *o o as detailed in Table 1 below for about 30 to 90 min at a temperature between 70 and 110 oC.

9 a 9 9 Table 1: Sample Reducing Bath Ingredient Amount in bath Defoamer 0.4 %owb Surfactant/Scouring Agent 1.0 owg Optical Brightener 1.5 owg Bisulfite 16 owg 12% Liquid Borohydride 4.0 owg The third step consists of contacting the fabric with the whitening bath such as detailed below in Table 2 for about an hour at about 70 110 °C.

Table 2: Whitening Bath Ingredient Amount in bath Citric Acid 0.35 owb Leveling Agent* 1.0 owg Ammonium Sulfate 1.0 owb Acetic Acid 0.25 owb Optical Brightener 0.5 owg Violet Acid Dye 0.001 owg Dye Auxiliary DN 99-076 -7- This step may be followed by at least one dyeing step, followed by several washing baths, the first of which contains 0.35% owb citric acid (or any mild acid).

After the last such bath, the fabric is checked for shade.

The method of contacting the fabric with the baths in the above steps can be done at any point during wet processing of the grey fabric, using any of a number of methods known to those skilled in the art. Such methods include, without limitation: producer dyeing; stock dyeing; yarn dyeing; and piece or garment dyeing such as by pad baths, jigs, becks (pressurized and non) and jets. It is not required that the same method be used for each such bath.

.10 The following examples are presented to illustrate further various aspects of the present invention, but are not intended to limit the scope of the invention in any respect. In the examples, the color evaluation readings are abbreviated as follows.

Color value Scale SL Lightness (greyscale) white 100; black 0 a red/green values are red; values are green b yellow/blue values are yellow; values are blue W1 whiteness index 100 most white (natural); 0 least white; >100 optical brightener added 00.* AE (total color difference) Square root of (L 2 a 2 b 2 The a and b values determine hue, and shifts of either of these values impact on the chroma (depth of hue). For purposes of the present invention, changes in L and WI are most significant in determining whitening of the treated fabric. Shifts in the value of b are also important, however, as white is often translated to mean a bluewhite.

DN 99-076 -8- Example 1 The following example demonstrates the bleaching capability of a reducing solution of the present invention.

Warp knit fabric (21.5 g of 80% nylon and 20% Lycra fabric) was added to about 500 mL of water in a bath vessel. To this bath was added 1% owg of surfactant, with stirring. The bath was heated to boiling (about 95 with stirring.

In a separate container, 0.67 g (3.11% owg) of sodium metabisulfite was mixed with about 10 g of water, and 0.18 g (0.83% owg) of 12% liquid sodium borohydride added to the mixture. Immediately upon addition of the borohydride to the S 10 bisulfite, that mixture was added to the fabric bath containing surfactant. The fabric was treated in this reducing bleach for up to about a half hour. Results are detailed in Table 3, below.

Table 3: Color Evaluation of warp knit fabric Color Standard 15 Minute 22 Minute Value (pretreatment) Reduction Reduction L 94.48 94.80 94.46 AL 0.32 -0.02 a -1.78 -1.82 -1.60 Aa -0.04 0.17 b 8.27 6.76 6.36 Ab -1.50 -1.92 WI 44.03 52.27 53.72 AWI 8.25 9.69 AE 1.54 1.93 The results demonstrate that the reducing bleach of the present invention significantly whitens fabric subjected to such treatment. In fact, there is a difference in whiteness between the untreated and treated fabric can be seen by the naked eye when the reducing bleach of the present invention is used, whereas use of conventional reducing bleaches results in such slight differences in whiteness that no noticeable difference can be observed unaided.

DN 99-076 -9- Example 2 The following example further illustrates the whitening ability of the reducing bleach of the present invention.

The procedure of Example 1 was followed, except that the reducing bath contained a total of 1.0% surfactant, 1.0% owg 12% liquid sodium borohydride and 3.66% owg of sodium metabisulfite. In addition, the fabric was treated for up to about 1 hour in the reducing bath.

Table 4: Color Evaluation of Warp Knit Fabric Color Standard 30 Minute 60 Minute Value (pretreatment) Reduction Reduction L 94.48 94.94 94.59 AL 0.46 0.11 a -1.78 -1.74 -1.61 Aa 0.04 0.17 b 8.27 7.01 6.81 Ab -1.26 -1.46 WI 44.03 51.20 51.58 A. sWI 7.18 7.55 E 1.34 1.48 The results further demonstrate the whitening ability of the reducing bleach :10 of the present invention.

Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.

The reference to any prior art in this specification is not, and should not be taken as, an acknowledgment or any form of suggestion that that prior art forms part of the common general knowledge in Australia.

Claims (10)

1. A system for bleaching fabric comprising greige fabric to be treated, a two component reducing solution, and means for heating said reducing solution to 70 to 110 wherein said first component of the reducing solution comprises between 0.1 and 0.6 owg borohydride and said second component of the reducing solution comprises bisulfite in water said bisulfite being present in a stoichiometric excess relative to the borohydride, and wherein the first component of the reducing solution is added to the second component just prior to treatment of the greige fabric.

2. The system of claim 1, wherein the bisulfite is of formula M(HSO3)x, wherein M is an alkaline metal, alkali earth metal or ammonium, and x is 1 or 2, depending on the valence of M.

3. The system of claim 1, wherein the first component of the reducing solution o comprises between 0.1 and 0.5 owg borohydride.

4. The system of claim 1, wherein the first component of the reducing solution comprises between 0.1 and 0.3 owg borohydride. The system of claim 1, wherein the borohydride is of formula T(BH 4 )y, wherein T is an alkaline metal, alkali earth inetal or ammonium, and y is 1 or 2, depending on the valence of T.

6. The system of claim 1, wherein the reducing solution is maintained at a temperature between 70 and 110 °C while said reducing solution is in contact with the fabric to be treated. DN 99-076 -11-

7. A method for bleaching greige fabric, comprising the steps of contacting greige fabric with a two-part reducing solution for a time sufficient to cause bleaching of the greige fabric to occur, wherein: such two-part reducing solution comprises a first component comprising between 0.1 and 0.6 owg borohydride and a second component comprising bisulfite in water, said bisulfite being present in a stoichiometric excess relative to the borohydride; and the first component of the reducing solution is added to the second component just prior to contacting the greige fabric with the reducing solution; and the two part reducing solution is maintained at a temperature between 70 and 110 °C during bleaching of the greige fabric.

8. The method of claim 7, wherein the first component of the reducing solution comprises between 0.1 and 0.5 owg borohydride.

9. The method of claim 7, wherein the bisulfite is of formula M(HSO 3 wherein M is an alkaline metal, alkali earth metal or ammonium, and x is 1 or 2, depending **on the valence of M. The method of claim 7, wherein the borohydride is of formula T(BH 4 )y, wherein T is an alkaline metal, alkali earth metal or ammonium, and y is 1 or 2, depending on the valence of T. -12- see* *of. 0.64 04 0 .0 C 0000 0.00 C SASS S 555e See.

11. A system and/or method substantially as hereinbefore described with reference to the Examples.

12. The steps, features, compositions and compounds disclosed herein or referred to or indicated in the specification and/or claims of this application, individually or collectively, and any and all combinations of any two or more of said steps or features. DATED this TENTH day of OCTOBER 2000 Rohm and Haas Company by DAVIES COLLISON CAVE Patent Attorneys for the applicant(s)