Technical Field The present invention relates generally to textile dyeing and more particularly to the dyeing of hydrophobic textile fibers in supercritical fluid carbon dioxide (SCF-C02).

Background Art It will be appreciated by those having ordinary skill in the art that conventional aqueous dyeing processes for textile materials, particularly hydrophobic textile fibers, generally provide for effective dyeing, but possess many economic and environmental drawbacks. Particularly, aqueous dyebaths

which include organic dyes and dyeing assistants must be disposed of according to arduous environmental standards. Additionally, heat must be applied to dry the textile material after dyeing in an aqueous bath. Compliance with environmental regulations and process heating requirements thus increase the costs of aqueous textile dyeing to both industry and the consuming public alike. Accordingly, there is a long-felt need in the art for an alternative dyeing process wherein such problems are avoided.

One alternative to aqueous dyeing that has been proposed in the art is the dyeing of textile materials, including hydrophobic textile fibers like polyester, in a supercritical fluid. Particularly, textile dyeing methods using SCF-CO2 have been explored.

However, those in the art who have attempted to dye textile materials, including hydrophobic textile fibers, in SCF-C02 have encountered a variety of problems. These problems include, but are not limited to,"crocking" (i. e. tendency of the dye to rub off when the dyed article is touched) of the dyed textile article; unwanted deposition of the dye onto the article and/or onto the dyeing apparatus during process termination; difficulty in characterizing solubility of the dyes in SCF-C02; difficulty introducing the dyes into the SCF- CO2 flow; and difficulty in preparing the dyes for introduction into the dyeing process. These problems are exacerbated when attempts to extrapolate from a laboratory dyeing process to a commercial scale process are made.

There have been several attempts in the prior art to address the problems associated with dyeing of textile materials, particularly hydrophobic textile fibers, in SCF-C02. One such attempt is described in Patent Publication

No. WO 97/13915 published April 17,1997, inventors Eqaers et al., assignee Amann and Söhne GMBH & Co. This publication describes a process for dyeing a textile substrate, particularly polyester yarns, using SCF-CO2. The process includes a pressure and/or temperature decrease and/or volume enlargement as part of the termination of the process. The described process attempts to provide a dyed textile substrate having a high color-fastness level.

However, this goal is pursued by removal of dye material from the fluid so that in the final stage of the process a fluid largely free from residual dye flows against or through the dyed textile substrate. Thus, complex additional systems, such as a secondary circulation system, are required to provide dye- free fluid to the process.

Moreover, dye-free fluid can be supplied to the autoclave or first circulation system associated with the autoclave before or during execution of the pressure decrease, temperature decrease, and/or volume enlargement.

Thus, there is a lack of criticality associated with the timing of the incorporation of the dye-free fluid into the system, as well as a lack of criticality associated with whether a pressure decrease, temperature decrease, and/or volume enlargement is selected for process termination. Finally, the spent sorbent material requires disposal after process termination, which can create environmental concerns analogous to those encountered with the use of conventional aqueous dyeing processes.

Poulakis et al., ChemiefasernlTextilindustrie, Vol. 43-93, Feb. 1991, pages 142-147 discusses the phase dynamics of SCF-CO2. An experimental section describing an apparatus and method for dyeing polyester in SCF-C02

in a laboratory setting is also presented. This method is thus believed to be limited in practical application.

U. S. Patent No. 5,199,956 issued to Schlenker et al. on April 6,1993 describes a process for dyeing hydrophobic textile materials with disperse dyes by heating the disperse dyes and textile material in SCF-CO2 with azo dyes having a variety of chemical structures. The patent thus attempts to provide an improved SCF-CO2 dyeing process by providing a variety of dyes for use in such a process.

U. S. Patent No. 5,250,078 issued to Saus et al. on October 5,1993 describes a process for dyeing hydrophobic textile materials with disperse dyes by heating the disperse dyes and textile material in SCF-CO2 under a pressure <BR> <BR> of 73 to 400 bar at a temperature in the range from 80°C to 300°C. Thenfhe pressure and temperature are lowered to below the critical pressure and the critical temperature, wherein the pressure reduction is carried out in a plurality of steps.

U. S. Patent No. 5,578,088 issued to Schrell et al. on November 26, 1996 describes a process for dyeing cellulose fibers or a mixture of cellulose and polyester fibers, wherein the fiber material is first modified by reacting the fibers with one or more compounds containing amino groups, with a fiber- reactivedispersedyestuffin SCF-CO2atatemperature of 70-210°C and a CO2 pressure of 30-400 bar. Specific examples of the compounds containing amino groups are also disclosed. Thus, this patent attempts to provide level and deep dyeings having very good fastness properties by chemically altering the fibers prior to dyeing in SCF-CO2.

U. S. Patent No. 5,298,032 issued to Schlenker et al. on March 29,1994 describes a process for dyeing cellulosic textile material with disperse dyes, wherein the textile material is pretreated with an auxiliary that promotes dye uptake subsequent to dyeing under pressure and at a temperature of at least 90°C, with a disperse dye from SCF-CO2. The auxiliary is described as being preferably polyethylene glycol. Thus, this patent attempts to provide improved SCF-CO2 dyeing by pretreating the material to be dyed.

What is needed, then, is an improved method of dyeing hydrophobic textile fibers with colorant materials in SCF-CO2 which addresses the problems <BR> <BR> identified, yet heretofore unsolved ; by the art. An improved method of dyeing hydrophobic textile fibers with colorant materials in SCF-CO2 which resolves the"crocking"problem identified in the art is particularly desired.

Disclosure of the Invention A process for dyeing a hydrophobic textile fiber with a colorant material, such as a disperse dye, using a SCF-CO2 dyebath is described. The process comprises the steps of selecting a colorant material that is soluble in SCF-CO2 at a first temperature range and sparingly soluble in SCF-CO2 or near-critical fluid CO2 at a second temperature range, wherein the first temperature range is higher than the second temperature range; heating the hydrophobic textile fiber and the colorant material in SCF-CO2 under SCF pressure conditions to a temperature within the first temperature range to initiate dyeing ; continuing the dyeing of the hydrophobic textile fiber by cooling the process to a temperature within the second temperature range without venting the SCF-

CO2, whereby SCF-CO2 density remains constant; and terminating the process after a predetermined dyeing time.

Optionally, the process may comprise the steps of selecting a colorant material that is soluble in SCF-CO2 at a first density range and sparingly soluble in SCF-C02 or near-criticai fluid CO2 at a second density range, the second density range comprising a lower density range that the first density range; heating the hydrophobic textile fiber and the colorant material in SCF- CO2 under SCF pressure conditions to a predetermined dyeing temperature; adjusting the density of the SCF-CO2 under SCF pressure conditions to a density within the first density range by adding CO2 to initiate dyeing of the hydrophobic textile fiberwith the colorant material; continuing the dyeing of the hydrophobic textile fiber by reducing the density of the SCF-CO2 to a density within the second density range by venting CO2 from the process without reducing the temperature of the process; and terminating the process after a predetermined dyeing time.

Accordingly, it is an object of the present invention to provide an improved process for dyeing a hydrophobic textile fiber with a colorant material using a SCF-CO2 dyebath.

It is another object of the present invention to provide an improved process for dyeing a hydrophobic textile fiber with a colorant material using a SCF-CO2 dyebath wherein the dyed fiber resists crocking.

It is another object of the present invention to provide an improved process for dyeing a hydrophobic textile fiber with a colorant material using a

SCF-CO2 dyebath that is particularly suited for batch dyeing in a commercial setting.

Some of the objects of the invention having been stated above, other objects will become evident as the description proceeds, when taken in connection with the accompanying drawings as best described hereinbelow.

Brief Description of the Drawinqs Figure 1 is a detailed schematic of a system suitable for use in the SCF- CO2 dyeing process of the present invention; Figure 2 is a detailed perspective view of a system suitable for use in the SCF-CO2 dyeing process of the present invention; Figure 3 is a schematic of an alternative embodiment of a system suitable for use in the SCF-CO2 dyeing process of the present invention; Figure 4 is a schematic of another alternative embodiment of a system suitable for use in the SCF-C02 dyeing process of the present invention; Figure 5 is a graph which shows qualitatively the dependence of dye solubility on SCF-C02 density and temperature; and Figure 6 is a graph which shows an exemplary temperature control profile for a dyeing run.

Detailed Description of the Invention Processes for dyeing a hydrophobic textile fiber with a colorant material using a SCF-CO2 dyebath are employed in accordance with the present invention to avoid crocking. One process employs cooling, without venting or

removing CO2 from the system, to a target CO2 temperature at or below the glass transition temperature of the hydrophobic fiber, followed by the venting of the dyeing system to atmospheric pressure. The other process employs venting, without cooling, to a target CO2 density where dye is no longer soluble in the SCF-CO2, followed by cooling to a target temperature and then venting to atmospheric pressure.

The process chosen depends on the solubility and affinity characteristics of the dye being used. The first process as described above is one of temperature reduction at constant density, while the second process as described above is one of density reduction at constant temperature. Thus, in accordance with the present invention, venting and not venting CO2 are density control steps which are used in the prevention of crocking. Alternatively, density reduction can also be achieved by expansion, that is, opening the system to additional volumes such as another vessel or more flow loop.

Thus, it is contemplated that a step in a dyeing process in accordance with the present invention that prevents crocking may be referred to as a depressurization step. This step occurs after the dyeing step and employs a path of either (1) cooling, without venting or expanding, to a target CO2 temperature followed by venting to atmospheric pressure; or (2) venting or expanding, without cooling, to a target CO2 density followed by complete venting to atmospheric pressure. The depressurization step is controlled via either process temperature or pressure. Pressure is regulated through venting or not venting CO2.

By way of further explanation, the depressurization steps used in accordance with the present invention fortemperature-controllable and density- controllable colorant material, one must consider the solubility behavior of the colorant materials (e. g. dyes) in SCF-CO,. Figure 5 shows qualitatively the dependence of dye solubility on SCF-CO2 density and temperature. In Figure <BR> <BR> 5, TH refers to the higher temperature and TL the lower temperature as discussed below in the Examples. Note that at some density the solubility curves for these two temperatures will cross each other. This temperature dependence is observed fordyes in SCF-CO2 as described herein, and indeed, <BR> <BR> for all solutes in supercritical fluids..--Examples of this behavior for naphthalene in supercritical ethylene and benzoic acid in SCF-CO2 are described in McHugh et al., Supercritical Fluid Extraction, 2d Ed., Butterworth-Heinemann, Boston, MA (1994), herein incorporated by reference.

The relative position of the crossover on the solubility plot and the actual usage level of the dye in a practical dyeing process varies, so that one dye may be used near point A, well above the crossover, and another dye may be used near point B, well below the crossover. The actual point on its solubility plot where any particular dye is used depends on its properties, such as molecular weight, heat of sublimation, melting point, and the like. Such information may be found in the Color Index.

If one is at point A on the curve for TH where the slope of solubility as a function of SCF-CO2 density is approximately zero, a decrease in SCF-C02 density at constant temperature (i. e., in the direction of the left-pointing arrow) gives little or no decrease in the solubility of the dye. On the other hand,

decrease in SCF-CO2 temperature (i. e., in the direction of the downward pointing arrow) results in decreased dye solubility. Temperature-controllable dyes are those for which the dyeing conditions (temperature, density of CO2- x-axis, and mole fraction of dye-y-axis) correspond to a relative point such as point A on the dye solubility plot. Cl Disperse Blue 77 is an example of such a dye. For dyes of this type, controlled reduction in temperature will result in controlled reduction of dye solubility, which causes the dye to partition favorably towards the textile fiber that is being dyed. It is noted that the temperature preferably remains above Tg, the fiber dyeing temperature, at all times. As the dye exhausts out of-solution, it is sorbed into the fiber because < the conditions are favorable to dye uptake.

Conversely, lowering density (e. g., by venting) at constant temperature will not result in significant reduction in solubility for a temperature-controlled dye until a point on the solubility curve is reached where the solubility versus density slope is positive. At this point the dye solubility drops rapidly with SCF-CO2 density reduction. Dye exhausts from the solution often at a rate that is greater than the rate that it can be taken up by the fiber. The dye may thus precipitate and crocking occurs. <BR> <BR> <BR> <P> If dye is used at a relative point B on the curve for TH where the slope<BR> <BR> <BR> is positive and the T, curve lies above the TH curve, a decrease in SCF-C02 temperature (i. e., in the direction of the upward pointing arrow) may result in an increase in dye solubility. Therefore, an associated"stripping"effect may occur whereby dye actually desorbs from the fiber into the solution. By contrast, decrease in SCF-CO2 density at constant temperature (i. e., in the direction of

the arrow that follows the TH curve) results in decrease in dye solubility.

Density-controllabie dyes are those forwhich the dyeing conditions correspond to a relative point such as point B on the dye solubility plot. Numerous dyes have been observed to exhibit this behavior; e. g., Cl Disperse Red 167, Cl Disperse Yellow 86, Cl Disperse Blue 60, and Cl Disperse Violet 91 (See Table 2). For dyes of this type, controlled reduction in density at constant temperature will result in controlled reduction in dye solubility, which causes the dye to partition favorably towards the textile fiberthat is being dyed. As the dye exhausts out of solution, it is sorbed into the fiber because the conditions are favorable to dye uptake; i. e., T > Tg.

On the other hand, lowering the temperature at constant density will result in significant increase in solubility for a density-controllable dye. If a path is followed where the dye bath is cooled then vented, crocking may occur because the dyeing rate will be too low as the dye exhausts out of solution, and thus, the dye will precipitate rather than be sorbed into the fiber.

Thus, the process whereby a dye partitions from the solution towards the fiber is complex, depending not only on its solubility in SCF-C02, but also on its affinity for the fiber, the fiber diffusion coefficient and time at each particular set of conditions; i. e., SCF-CO2 temperature and density. Therefore, it is further suggested that there are depressurization paths, other then the ones described above for points A and B, whereby crocking may be avoided. For example, from points A and B, paths are followed where both cooling and density reduction (venting) simultaneously are employed. Such paths may have certain advantages, such as from the standpoint of reducing process

time, as compared to the depressurization paths described above for temperature-controllable and density-controllable dyes. However, the processes described above and in Examples 1 and 2 produce high quality and improved dyeings of hydrophobic textile materials in SCF-C02 as compared to prior art processes and thus are believed to represent a significant advance in the art.

While the following terms are believed to have well defined meanings in the art, the following definitions are set forth to facilitate explanation of the invention.

The terms"supercritical fluid carbon dioxide"or"SCF-C02"mean CO2 < under conditions of pressure and temperature which are above the critical pressure (P = about 73 atm) and temperature (Tc = about 31 °C). In this state the CO2 has approximately the viscosity of the corresponding gas and a density which is intermediate between the density of the liquid and gas states.

The term"hydrophobic textile fiber"is meant to refer to any textile fiber comprising a hydrophobic material. More particularly, it is meant to refer to hydrophobic polymers which are suitable for use in textile materials such as yarns, fibers, fabrics, or other textile material as would be appreciated by one having ordinary skill in the art. Preferred examples of hydrophobic polymers include linear aromatic polyesters made from terephathalic acid and glycols; from polycarbonates; and/or from fibers based on polyvinyl chloride, polypropylene or polyamide. A most preferred example comprises one hundred fifty denier/34 filamenttype 56 trilobal texturized yarn (polyesterfibers) such as that sold under the registered trademark DACRON@ (E. I. Du Pont De

Nemours and Co.). Glass transition temperatures of preferred hydrophobic polymers, such as the listed polyesters, typically fall over a range of about 55°C to about 65°C in SCF-CO2.

The term"colorant material"is meant to refer to sparingly water-soluble or substantially water-insoluble dyes. Examples include, but are not limited to, forms of matter identified in the Colour Index, an art-recognized reference manual, as disperse dyes. Additional examples are found Tables 1 through 3, as set forth hereinbelow. Preferably, the colorant material comprises press- cake solid particles which has no additives.

The term"sparingly soluble", ;. when used in referring to a dye, means that < the dye is not readily dissolved in a particular solvent at the temperature and pressure of the solvent. Thus, the dye tends to fail to dissolve in the solvent, or alternatively, to precipitate from the solvent, when the dye is"sparingly soluble"in the solvent at a particular temperature, density and/or pressure.

The term"crocking", when used to describe a dyed article, means that the dye exhibits a transfer from dyed material to other surfaces when rubbed or contacted by the other surfaces.

The term"fiber diffusion coefficient"is meant to refer to the flux of dye into a fiber and is analogous to a heat transfer coefficient.

Following long-standing patent law convention, the terms"a"and"an" mean"one or more"when used in this application, including the claims.

The following Examples have been included to illustrate preferred modes of the invention. Certain aspects of the following Examples are described in terms of techniques and procedures found or contemplated by the

present inventors to work well in the practice of the invention. These Examples are exemplified through the use of standard laboratory practices of the inventors. In light of the present disclosure and the general level of skill in the art, those of skill will appreciate that the following Examples are intended to be exemplary only and that numerous changes, modifications and alterations can be employed without departing from the spirit and scope of the invention.

Example 1-Temperature Controllable Dyes As disclosed in this Example, the novel dyeing process includes, first of all, the selection of a colorant material which is soluble in SCF-CO2 at a high temperature, and which is sparingly soluble in SCF-C02 or near-critical fluid CO2 at a lower temperature. A preferred high temperature range comprises about 60°C to about 200°C. A more preferred high temperature range comprises about 90°C to about 140°C. A most preferred high temperature range comprises about 100°C to about 130°C. Indeed, as described in Tables 1A through 1C below, the average high temperature is about 100°C. As will be observed in the Tables below, the high temperature is also referred to herein as the"dyeing temperature"or"Tdyeing"in that dyeing is initiated by heating the process to the high temperature and that dyeing continues for a predetermined time at this temperature. It should also be noted that the high temperature is preferably lower than the melting/degradation temperature of the dye itself, and is preferably lower than the melting temperature of the hydrophobic textile fiber, e. g. 252°C for polyester.

The preferred lower temperature range comprises about 30°C to about 80°C. Indeed, it is preferred that the lower temperature range falls within temperatures that maintain the SCF-CO2 in a SCF state and that the lower temperature range falls above the glass transition temperatures of the textile material being dyed. Thus, a more preferred range for the lower temperature range comprises about 70°C to about 75°C.

The pressure of the process is preferably at least high enough that the C02'S in the SCF state. Exemplary pressure ranges include from about 73 atm to about 400 atm. Preferred process parameters are set forth in the Tables 1A, 1 B and 1 C which follow.

Abbreviations used in Tables 1 A, 1 B and 1 C atm-Atmosphere. <BR> <BR> <BR> <BR> <BR> <P>Ppackage-Density of hydrophobic textile fiber package to be dyed in grams per cubic centimeter (g/cm3).

PCo2 Density of CO2 in grams per cubic centimeter (g/cm3).

I/O-Inside-to-outside circuit.

New-Taper of hydrophobic textile fiber package = 40% Outside-to-insidecircuit.O/I- Old-Taper of hydrophobic textile fiber package = 100% Packagewt-Weight of hydrophobic textile fiber package in grams (g). psi-Pounds per square inch.

Qco2-Flow rate of CO2 in gallons per minute (gpm).

ReverseCO2flowsintheexpansionvessel.(R)- res.-Residue.

Tdyeing(°C)-Temperature in highertemperature range atwhich dyeing is initiated. t-Time elapsed during dyeing process.

* - Fill with CO2 at T = 50°C -High density packages.

TABLE 1A<BR> AVERAGE EXPERIMENTAL CONDITIONS AND<BR> PACKAGES CHARCTERISTICS Disperse dye Blue 77 Pressure Tdyeing (°C) #CO2 #package Packagewt Dye holde Run (alm/psi) (g/cm3) Qco2 (gpm) (g/cm3) (g) device 001 306/4500 130-135 0.5297 4.87:I/O(t=80 min) 0.3990 515 One fiber b@ 002A 310/4550 110-115 0.6225 5.02:I/O(t=80 min) 0.3562 475 Screen co@ 002B 308/4525 125-130 0.5763 1.21/4.11(t=80 min) 0.3562 475 Bottom filte 003(R) 316/4650 105-110 0.6332 2.91/5.66(t=120 min) 0.3504 460 2 flat scree@ 004 313/4600 100-115 0.6118 3.30:I/O(t=60 min) 0.3555 475 Dosage-pur 005 320/4700 110-115 0.6373 3.09:I/O(t=60 min) 0.3763 515 Dosage-pur 006(R) 305/4475 110-115 0.6180 2.75:I/O(t=90 min) 0.3941 515 Fluidized b@ 007(R) 283/4163 115-125 0.6245 0.62/3.66(t=180 min) 0.3885 515 Fluidized b@ 008(R) 270/3970 60-110 0.692 4.78{1[30(I)x2(O)]} 0.4051 520 Fluidized b@ 009 292/4289 105-110 0.6439 3.20:I/O(t=300 min) 0.3950 390 Flat plate

TABLE 1A (continued) 010* 287/4220 92-100 0.6311 3.31:I/O(t=120 min) 0.4190 429 Flat plate 011* 299/4400 94-100 0.6511 4.75{6[6(I)x2(O)]} 0.4780 445 Flat plate 012 320/4706 97-98.1 06640 4.40{6[6(I)x3(O)]} 0.501 470 Cone-plate 013 313/4598 98.3-101 0.6936 0.84{8[6(I)x2(O)]} 0.595* 560 Fluidized b@ 014 297/4363 92.4-118 0.6308 5.01{12[6(I)x2(O)]} 0.610 575 Cone-plat@ 015 296/4355 105-110 0.6399 3.22{3[6(I)x2(O)]] 0.604 565 Cone-plat@

TABLE 1B<BR> AVERAGE EXPERIMENTAL CONDITIONS AND<BR> PACKAGES CHARACTERISTICS Disperse dye Red 167 Pressure #CO2 #package Packagewt. Run (atm/psi) Tdyeing (°C) (g/cm3) Qco2 (gpm) (g/cm3) (g) Dye hold device 016 309/4539 125-130 0.5939 2.87{3[6(I)x2(O)]} 0.604 565 Plate/Filt 017 316/4645 125-130 0.5858 4.56{4[6(I)x2(O)]} 0.570 535 Plate/Filt 018A/B 2572/3376 105-110 0.43/0.51 4.20{4[6(I)x2(O)]} 0.511 480 Plate/Filt 019 212/3120 100 0.49 4.21{4[6(I)x3(O)]} 0.560 525 Plate/Filt 020 245/3594 100-110 0.53-0.54 5.10{6[6(I)x2(O)]} 0.590 555 plate/Filt 021 226/3325 100 0.5111 5.26{6[6(I)x2(O)]} 0.588 550 Plate/Filt

TABLE 1C<BR> AVERAGE EXPERIMENTAL CONDITIONS<BR> AND PACKAGES CHARACTERISTICS Disperse dye Violet 91 Pressure Tdyeing #CO2 #package Packagewt. Remarks Run (atm/psi) (°C) (g/cm3) Qco2 (gpm) (g/cm3) (g) DV-2 317/4665 100-102 0.6430 7.24:I/O (t=16 min) 0.592 540 (old) Small dye @ DV-3 313/4595 100-101 0.6395 6.71:I/O (t=16 min) 0.649 570 (new) Small dye @ DV-4 292/4293 90-92 0.6599 6.51:I/O (t=16 min) 0.660 500 (new) Dye resid@ DV-5 316/4648 110-111 0.6239 7.58:I/O (t=16 min) 0.508 390 (new) No dye re DV-6 316/4640 106-110 0.6220 6.20:I/O (t=16 min) 0.657 590 (old) No dye re DV-7 243/3578 80-82 0.6257 6.14:I/O (t=16 min) 0.635 570 (new) Large dye @ DV-8 292/4285 95-96 0.6392 6.22:I/O (t=16 min) 0.635 570 (new) Large dye @ Average cycle dyeing time = 16 minutes<BR> Average dyeing temperature = 100°C<BR> Average CO2 density (#) - 0.62 g/cm3<BR> Average pressure = 4300 psi = 306 atm = 310 bar<BR> Average CO2 flow rate = 6 - 10 gal/min

After a suitable colorant material is selected, the hydrophobic textile fiber and the colorant material are each placed in a suitable containment vessel in the dyeing system and are heated in SCF-CO2 under SCF pressure conditions to a temperature within the higher temperature range. The amount of CO2 added will be sufficient to achieve the desired operating density, typically a value in the range of about 0.6 g/cm3 to about 0.65 g/cm3. The amount of colorant material added, and thus, the dye concentration used in the process, will vary depending on the desired shade and is based on the limits of solubility of dye in both the SCF-CO2 and the fiber. Additionally, and preferably, the colorant material is readily or highly soluble in the SCF-CO2 at the high temperature. Stated differently, within the higher temperature range, the colorant material has a high affinity for the SCF-CO2 solvent.

Dyeing of the polyester initiates once the SCF-CO2 flow reaches a temperature sufficient to: (1) dissolve the colorant material, typically at or above 50°C, and (2) cause the hydrophobic polymers of the hydrophobic textile fiber to be receptive to diffusion of colorant material into their interior, typically at or above 80°C. Stated differently, the hydrophobic polymers are receptive to the diffusion of colorant material into their interior at temperatures above their glass transition temperatures. The glass transition temperatures of preferred hydrophobic polymers, such those listed above, typically fall over a range of about 55°C to about 65°C in SCF-CO2. The temperature of the process is maintained at the temperature within the higher temperature range for a predetermined period of time, such as 0 to about 45 minutes, or 0 to about 30 minutes.

The dyeing of the hydrophobic textile fiber continues by isolating the vessel containing the colorant material and cooling the process to a temperature within the lower temperature range before anyventing ofthe SCF- CO2 occurs. The term"venting"refers to the removal of CO2 from the dyeing system. Thus, because the process represents a closed system, the density of the SCF-CO2 is maintained at a constant level. As noted above, the colorant material is sparingly soluble in the SCF-CO2 or the near-critical fluid CO2 at the lower temperature. But, the dyeing rate is still high because the decrease in solubility of the dye produced by the cooling step causes the dye to partition much more in favor of the textile fiber that is being dyed. Indeed, the decreased solubility causes the dye to partition toward the textile fiber until the dye is in essence completely exhausted from the SCF-CO2 dyebath. Stated differently, within the lower temperature range, the colorant material has a higher affinity for the hydrophobic textile fiber to be dyed as compared to the SCF-CO2 solvent. The insolubilization of the dye and partitioning of the dye towards the hydrophobic textile fiber thus results in complete dyebath exhaustion. Additionally, isolation of the vessel containing the colorant material from the remainder of the dyeing process will prevent any residual colorant material in this vessel from entering the SCF-CO2 as the dyebath is exhausted.

Once there is no dye in the bath, there is no fouling of the equipment or substrate by unwanted dye precipitation, thus reducing the crocking potential for the dyed textile fiber. There is no need for a scouring or after-clearing step for the dyed textile fiber or the dyeing equipment. Overall dye cycle time is therefore reduced.

The cooling step occurs without removal of C02 from the system by venting or expanding the SCF-CO2. In sharp contrast, prior art processes are depressurized by venting CO at elevated temperatures while there is still residual dye in the SCF-C02 dyebath. This can lead to equipment fouling and crocking of the dyed article, a common problem seen in other attempts to dye from SCF-CO2.

The process of the present invention can further comprise depressurizing the process by venting after a predetermined time. Preferably, the predetermined time comprises a time after which complete exhaustion of the colorant material from the SCF ;-CO2 dyebath is attained, for example, by \ cooling. More preferably, the venting of the process is carried out gradually in a series of steps or in a continuous pressure ramp. For example, the pressure in each step is preferably reduced by steps of density, (p), i. e., the removal of <BR> <BR> <BR> CO2 at Ap of 0.05 g/cm3 every 5 minutes; or by pressure drop between 15 atm to 30 atm every 5 minutes.

Crocking in polyester textile materials dyed with colorant materials in SCF-CO2 is therefore avoided by cooling, without venting or expanding, the SCF-CO2 dyebath to a temperature within the lower temperature range at which the dye has a very low solubility. Yet, the temperature remains above the dyeing temperature (glass transition temperature of the hydrophobic textile substrate in SCF-CO2), so that the insolubilization of the dye results in complete dyebath exhaustion. Additionally, within the lower temperature range, a suitable colorant material has a higher affinity for the hydrophobic textile fiber to be dyed as compared to the SCF-CO2 solvent. This process

works particularly well for dyes such as Cl Disperse Blue 77 (B77) of Table 2.

Table 2 presents a list of several disperse dyes that were selected based on equilibrium solubility of the disperse dyes in CO2. Dye B77 in Table 2 may be characterized as a"temperature controllable dye"as described above and in Figure 5; and is particularly suitable for use in the process of the present invention, as described in this Example.

Abbreviations used in Table 2 B-Blue (color of dye) p dye dissolve-Density'of SCF-CO2 in grams per cubic centimeter (g/cm3) at which dye dissolves. p dyeing-Density of SCF-CO2 in grams per cubic centimeter (g/cm3) at which dyeing is initiated.

EST. STR. DYE-Estimated strength of dye.

I/0-Inside-to-outside circuit.

NC-No crocking observed.

0/1-Outside-to-inside circuit.

Qco2-Flow rate of CO2 in gallons per minute (gpm).

R-Red (color of dye) REV. FLOW-Reverse CO2 flows in the expansion vessel. <BR> <P> Tcool (°C)-Temperatureinlowertemperaturerangeatwhich dyeing is continued. <BR> <P> Tdyemg(°C)-Temperature in highertemperature range at which dyeing is initiated.

Time (min) Dye-Time elapsed during dyeing process in minutes (min).

V - Violet (color of dye) Y-Yellow (color of dye) TABLE 2 Disperse Run # # dye # T(°C) Time Depress- T Qco2 REV. EST. R? Dye dissolve dyeing dyeing (min) urizaiton (°C) (gpm) FLOW STR. C? (g/cm3) (g/cm3) dye step cool I/O-O/I DYE down B77 15 0.39 0.60 110 16 Cool 75 6.95 Yes 2:1 N? without Venting or Expanding R167 20 0.30 0.54 106 48 Vent or 50 5.10 Yes 4:1 N? Expand without Cooling Y86 25 0.49 0.60 102 8 Vent or 75 5.09 Yes 1.8:1 N? Expand without Cooling B60 28 0.42 0.63 108 16 Vent or 75 4.97 No 2.8:1 N? Expand without Colling V91 30 0.40 0.62 106 8 Vent or 65 5.35 Yes 1.6:1 N? Expand without Cooling

R324 34 0.35 0.66 110 16 Vent or 80 5.5 No 1.1:1 N? Expand without Cooling B102 36 0.35 0.67 110 16 Vent or no 5.0 No N? Expand without Cooling B165:1 35 0.39 0.66 110 8 Vent or 80 4.9 Yes 2.8:1 N? Expand without Cooling B118 32 0.33 0.66 110 24 Vent or 90 4.5 No 2:1 N? Expand without Cooling Y42 39 0.37 0.66 106 16 Vent or 90 5.6 No N? Expand without Cooling Burgundy 38 0.40 0.68 100 16 Vent or 79 5.0 No N? Expand without Cooling

Referring now to the drawings, wherein like reference numerals referto like parts throughout, a system suitable for carrying out the process of the instant invention is referred to generally at 10. In the following detailed description, the parts of system 10 that are primarily involved in the process of the present invention are described. Additionally, a legend describing other parts of system 10 is provided below.

Referring particularly to Figures 1 and 2, operation and control of heating/cooling of the SCF-CO2 dyeing system 10 preferably encompasses three distinct equipment subsystems. The subsystems include filling and pressurization subsystem A, dyeing subsystem B, and venting subsystem C.

< Carbon dioxide is introduced into system 10 via CO2 supply cylinder 12.

Preferably, supply cylinder 12 contains liquid carbon dioxide. Thus, liquide02 enters the filling and pressurization subsystem A from the supply cylinder 12 through line section 14 and regulating valve 16 and is cooled in condenser 26 by a water/glycol solution supplied by chiller 28. The CO2 is cooled to assure that it remains in a liquid state and at a pressure sufficiently low to prevent cavitation of system pressurization pump 34.

Continuing with Figures 1 and 2, turbine flow meter 30 measures the amount of liquid CO2 charged to dyeing system 10. Pump 34 increases the pressure of the liquid CO to a value above the critical pressure of COZ but less than the operating pressure for the dyeing system, typically about 4500 psig.

A side-stream of water/glycol solution from chiller 28 provides cooling for pump 34. Control valve 36 allows pump 34 to run continuously by opening to bypass liquid CO2 back to the suction side of pump 34 once the system pressure set

point has been reached. This valve closes if the system pressure falls below the set point that causes additional liquid CO to enter the dyeing subsystem B. If co-solvent is potentially used, it is injected into the liquid C02 stream by pump 50 at the discharge of pump 34 and mixed in by static mixer 38. All of the process steps described herein remain unchanged by the introduction of a co-solvent.

Continuing with Figures 1 and 2, liquid C02 leaving mixer 38 enters electrical pre-heater 40 where its temperature is increased. Heated and pressurized CO2 may enter the dyeing subsystem B through needle valve 66 and into dye-add vessel 70; through needle valve 64 and into dyeing vessel 106; orthrough both of these paths. Typically, dyeing subsystem B is filled and pressurized simultaneously through both the dye-add and dyeing vessels 70 and 106, respectively.

Once a sufficient quantity of liquid CO2 has been charged to dyeing subsystem B to achieve the operating density, typically a value in the range of 0.6 to 0.65 g/cm3, circulation pump 98 is activated. Pump 98 circulates liquid CO2 through dye-add vessel 70, which contains a weighed amount of colorant material, and then through dyeing vessel 106, which contains the package of yarn to be dyed. Once circulation is started, heating of subsystem B is initiated by opening control valves 78 and 84 to supply steam to and remove condensate, respectively, from the heating/cooling jacket 71 on dye-add vessel 70. Similarly, control valves 132 and 136 are opened to supply steam to and remove condensate from, respectively, the heating/cooling jacket 107 on dyeing vessel 106. Commercial practice would utilize a heat exchanger in the

circulation loop to provide for heating of the SCF-CO2 rather than relying on heating through the vessel jackets 71 and 107. Heating is continued until the system passes the critical temperature of CO2 and reaches the operating, or dyeing, temperature, typically about 100°C to about 130°C.

SCF-CO2 leaving circulation pump 98 passes through sight glass 96 and is diverted, by closing ball valve 94 and opening ball valve 93, through dye-add vessel 70 where dye is dissolved. Dye-laden SCF-CO2 passes out of the dye- add vessel 70 through ball valve 92 and flow meter 118 to ball valve 120. Ball valve 120 is a three-way valve that diverts the SCF-CO2 flow to the inside or outside of the package loaded in dyeing vessel 106 depending on the direction in which it is set. lf ball valve 120 is set to divert flow in the direction of ball valve 104, and ball valve 104 is open and ball valve 102 is closed, then all of the SCF-CO2 flow proceeds to the inside of the dye spindle (not shown in Figs.

1 and 2). The flow continues from the inside to the outside of the dye spindle, from the inside to the outside of the dye tube (not shown in Figs. 1 and 2) on which the polyester yarn package is wound and out through the polyester yarn package to the interior of dyeing vessel 106. The SCF-CO2 flow passes out of dyeing vessel 106, through open ball valves 114 and 116 to the suction of pump 98, completing a circuit for inside-to-outside dyeing of the polyester yarn package.

If ball valve 120 is set to divert flow in the direction of ball valve 114, and ball valve 114 is open and ball valve 116 is closed, then all of the SCF-C02 flow proceeds to the interior of dyeing vessel 106 and the outside of the polyester yarn package. The flow passes through the polyester yarn package,

continues from the outside to the inside of the dye tube on which the yarn is wound and then passes from the outside to the inside of the dye spindle. The SCF-CO2 flow exits the interior of the dye spindle and passes through open ball valves 104 and 102 to the suction of pump 98, which completes a circuit for outside-to-inside dyeing of the polyester yarn package.

Dyeing of the polyester initiates once the SCF-CO2 flow passing the dye- add vessel 70 reaches a temperature sufficient to: (1) dissolve colorant material, typically at or above 50 °C, and (2) cause the polyester to be receptive to diffusion of colorant material into its interior, typically at or above 80°C. The dye-laden SCF-C02 flow is held at ; values ranging from values of 1 gallon per minute (GPM)/lb of polyester or less, to values greater than 15 GPM/lb of polyester. As described in Tables 1 A, 1 B and 1 C above, the dye-laden SCF- CO2 flow is periodically switched between the inside-to-outside (I/O) circuit and the outside-to-inside (O/l) circuit to promote uniformity of dyeing of the polyester yarn; e. g., 6 min./2 min. I/O, 6 min./4 min. I/O, 5 min./5 min. I/O, etc.

This dyeing process is continued with system 10 held at the dyeing temperature, typically about 100°C to about 130°C, until the colorant material is exhausted onto the polyester yarn to produce an even distribution of the desired shade, typically around 30 minutes.

Once the colorant material is exhausted onto the polyester yarn, as dictated by its solubility and affinity characteristics, the dyeing system is cooled without venting. This depressurization step causes the dye remaining in solution in the SCF-CO2 to exhaust into the polyester fiber.

Before initiation of cooling of the dyeing process, dye-add vessel 70 is isolated for the remainder of the dyeing process by closing ball valves 92 and 93 while opening ball valve 94. This action allows the SCF-CO2 to maintain a circulation loop through dyeing vessel 106, but not through dye-add vessel 70.

This will prevent any additional dye remaining in dye-add vessel 70 from going into solution in the SCF-CO2 and will prevent the introduction of any residual dye that might remain in dye-add vessel 70 into the SCF-CO2 during the cooling and/or venting steps.

Cooling is initiated by continuing the SCF-CO2 circulation while cooling dyeing vessel 106. Thus, the action of circulation pump 98 maintains system flow during cooling. Additionally, because system 10 is a closed system, the density of the SCF-C02 remains constant during the cooling step. Cooling of dyeing vessel 106 is accomplished by closing control valves 132 and 136 to shut off the steam supply and condensate removal, respectively, to jacket 107.

Control valves 134 and 138 are opened to inject into and remove cooling water from, respectively, jacket 107. Cooling of dye-add vessel 70 is accomplished by closing control valves 78 and 84 to shut off the steam supply and condensate removal, respectively, to jacket 71. Control valves 80 and 82 are opened to inject into and remove cooling water from, respectively, jacket 71.

Commercial practice would utilize a heat exchanger in the circulation loop to provide for cooling of the SCF-CO2 rather than relying on cooling through the vessel jackets 71 and 107. To minimize heat up time between subsequent dyeings, the dyeing and dye-add vessels would not be cooled in commercial

practice so that the walls and lids of these vessels would retain as much heat as possible.

Once the system is cooled to the target temperature in the lower temperature range, preferably 70-75°C, and substantially complete dye exhaustion is attained, venting is initiated. Venting is accomplished by opening needle valve 109 to provide a flow path from the dyeing vessel 106 to control valve 154. Control valve 154 is opened to set the pressure in dyeing subsystem B and control valve 166 is opened to set the pressure in separator vessel 156. By adjusting control valves 154 and 166 appropriately, the pressure in the dyeing vessel 106 is reduced at a controlled rate, typically with 4 average values in the range of 0.01 to 1.0 Ib/min. Dye-add vessel 70 is isolated during venting to prevent any additional dye remaining in dye-add vessel 70 from going into solution in the SCF-CO2. Isolation of dye-add vessel 70 is accomplished by closing ball valves 92 and 93 while opening ball valve 94 to maintain a circulation loop for the dyeing vessel.

During venting SCF-CO2 flows from dyeing subsystem B through control valve 154 and into separator vessel 156 of venting subsystem C. In separator vessel 156 the pressure is sufficiently low so that the CO2 is in the gaseous phase and any remaining colorant material will no longer be soluble in it The <BR> <BR> colorant material solids collect in separator vessel 156 and gaseous CO2 exits through control valve 166. Once the gaseous CO2 passes through control valve 156 it may vented to atmosphere by opening needle valve 168. The gaseous CO2 may also be recycled to filling and pressurization subsystem A by keeping needle valve 168 closed so that the gaseous CO passes through

filters 172 and 174. Filters 172 and 174 collect any minute amounts of solids <BR> <BR> <BR> that may have escaped separator vessel 156 with the gaseous CO2 flow. The<BR> <BR> <BR> gaseous CO2 exiting filters 172 and 174 passes through check valve 178 and enters filling and pressurization subsystem A for re-use in system 10.

Referring now to Figure 3, an alternative system 10'for use in the SCF- CO2 dyeing process of the present invention is depicted schematically.

Generally, however, system 10'works in a similar manner as system 10 described above and as depicted in Figures 1 and 2. System 10'includes a CO2 cylinder 12', from which CO2 flows through check valve 16'to a cooling unit 26'. CO2 is cooled and pressurized within cooler 26'and then is pumped, using positive displacement pump 34', into dye injection vessel 70'. Prior to introduction of CO2 into vessel 70', a dyestuff is placed within vessel 70'. Thus, when CO2 is introduced into vessel 70'the dyestuff is suspended and/or dissolved within the carbon dioxide. The action of pump 34'drives the carbon dioxide/dye solution or suspension out of dye injection vessel 70'through a hand valve 64'and a check valve 182'into a dyeing vessel 106'which contains the textile fibers to be dyed. Dyeing vessel 106'is pressurized and heated to SCF dyeing conditions prior to the introduction of the carbon dioxide/dye solution or suspension. Thus, when the carbon dioxide/dye solution or suspension enters dyeing vessel 106', the dye either remains in solution or dissolves in the SCF-CO2, as the case may be. Steam and/or cooling water are introduced to jacket 107'of dyeing vessel 106'via valves 132'and 134', respectively. Thus, appropriate temperatures for dye dissolution and dyeing are achieved in vessel 106'. Particularly, cooling water is introduced via valve

134'to provide a lower temperature at which the dye is sparingly soluble in SCF-C02 or near-critical fluid CO2. At this temperature, dye partitions toward the textile fibers within dyeing vessel to be dyed. During and after dyeing, any condensate resulting from the introduction of steam through valve 132'is exported through vent 136'and any water introduced via valve 134'is exported through drain 138'.

Continuing with particular reference to Figure 3, during dyeing, the SCF- CO2/dye solution is circulated into and out of vessel 106'via circulation pump 98', valves 104'and 114', and 3-way valve 120'in a manner analogous to that described above for system 10, valves 104 and 114, and 3-way valve 120. i Flow meter 118'is placed in system 10'between circulation pump 98'and 3- way valve 120'so that the flow rate of SCF-CO2/dye solution can be monitored.

Dyeing is thus facilitated by circulation subsystem. Further, the action of circulation pump 98'maintains system flow during cooling.

Continuing with particular reference to Figure 3, after a predetermined time, preferably when complete dyebath exhaustion is observed, SCF-CO2 is removed from dyeing vessel 106'and flows through back pressure regulator <BR> <BR> 154'. At this point, the pressure of the process is reduced and CO2 within the system is introduced into separator vessel 156'. Any residual dye, likely a small amount, is removed from the CO2 in separator vessel 156'. CO2 then may be vented through vent 170'. Alternatively, CO may be recycled back into system 10'via check valve 178'.

Referring now to Figure 4, another alternative embodiment of a suitable system for use in the process of the instant invention is described. System 10"

includes CO2 cylinder 12". CO2 flows from cylinder 12"through check valve 16"into subcooler 26". The temperature of the CO2 is reduced within subcooler 26"to assure that is remains in a liquid state and at a pressure sufficiently low to prevent cavitation of positive displacement pump 34". The positive displacement pump 34"then drives the C02 through hand valve 64", then through a check valve 182", into dyeing vessel 106". Dyeing vessel 106" includes the textile fibers to be dyed.

Continuing with particular reference to Figure 4, dyeing vessel 106"is pressurized and heated to produce CO2 at SCF temperature and pressure.

SCF-CO2 is then exported from vessel 106"using circulation pump 98"and valves 104"and 114"in a manner analogous to that described above for system 10 and valves 104 and 114. SCF-CO2 is introduced via valve 92"into a dye injection vessel 70"containing a suitable dye. The dye is then dissolved in SCF-CO2. Circulation pump 98"drives the SCF-CO2 dye solution from vessel 70"through flow meter 118"and 3-way valve 120"back into dyeing vessel 106"wherein dyeing of the textile fibers is accomplished. During dyeing, steam and/or cooling water are introduced to jacket 107"of dyeing vessel 106"via valves 132"and 134", respectively. Thus, appropriate temperatures for dye dissolution and dyeing are achieved in vessel 106".

Particularly, cooling water is introduced via valve 134"to provide a dyebath at a lower temperature at which the dye is sparingly soluble in the resulting SCF- CO2 or near-critical fluid CO2 dyebath. At this temperature, dye partitions toward the textile fibers that is being dyed within dyeing vessel 106". During and after dyeing, any condensate resulting from the introduction of steam

through valve 132"is exported through vent 136"and any water introduced via valve 134"is exported through drain 138".

After a predetermined time, preferably when complete exhaustion of the SCF-CO2 dyebath is observed, the SCF-CO2 dyebath is removed from vessel 106"to back pressure regulator 154". The pressure of the process is then reduced using regulator 154"and the resulting CO2 phase is then introduced into separator vessel 156". In separator vessel 156"the pressure is further reduced so that any residual dye, likely a small amount, is deposited within separator vessel 156"and the resulting dye-free CO2 gas is removed from separator vessel 156". Particularly.; the dye-free CO2 gas may be vented using < vent 170"or may be recycled back into system 10"via check valve 178". The efficiency of the process of this invention is thus demonstrated.

Example 2-Density Controllable Dyes As disclosed in Example 1, crocking in hydrophobic textile fibers, such as polyester fibers, dyed with colorant materials in SCF-C02 is avoided by cooling, without venting, the SCF-CO2 dyebath to a temperature at which the dye has a very low solubility where the temperature remains above the dyeing temperature (glass transition temperature of the hydrophobic textile fiber in SCF-CO2) so that the insolubilization of the dye results in complete dyebath exhaustion. Such dyes are characterized above as"temperature controllable dyes".

However, there are other dyes, such as Cl Disperse Yellow 86, which remain somewhat soluble even at a low temperature, such as 40°C. There are

also dyes, such as Cl Disperse Red 167, which contain component isomers which remain soluble even at low temperature, such as 40°C. Additional examples are set forth in Table 2 above. In accordance an alternative embodiment of the present invention as disclosed in this Example, crocking problems associated with utilizing such dyes in SCF-CO2 dyeing may be avoided by controlling the density of the SCF-CO2 dyebath. Such dyes may be characterized as"density-controllable dyes", as described above and in Figure 5.

The preferred steps of this alternate embodiment of the present invention comprise placing the substrate or textile fiber to be dyed and the colorant material each in suitable containment vessels in dyeing system or apparatus, such as system 10 disclosed in Example 1 above. The dyeing system is then filled with CO2 to a density of about 0.1 g/cm3 and to a dyeing temperature of, for example, about 100°C. Bath circulation is then begun at the desired flow rate, which typically ranges, for example, from about 6 to about 20 gallons per minute (GPM).

The density of the SCF-CO2 is then raised to a final desired dyeing density by adding CO2 to the dyeing system. Preferably, the desired density falls with in a density range of about 0.4 g/cm3 to about 0.7 g/cm3. More preferably, the desired density comprises about 0.62 g/cm3. As the SCF-CO2 density increases, the colorant material begins to dissolve in the SCF-CO2.

Once the desired density is attained, the dyeing cycle begins and is continued for 30 to 45 minutes to achieve equilibrium or near equilibrium in the fiber and dyebath.

The density is then reduced slowly over time (e. g., 10 minutes) to a lower density, such as a density falling within a density range comprising about 0.3 g/cm3 to about 0.5 g/cm3, while holding temperature at or near the dyeing temperature. Preferably, the density within the lower density range comprises about 0.45 g/cm3. The dyeing temperature corresponds to a temperature within the high temperature range set forth in the embodiment of the invention described in Example 1 above. Optionally, the alternative embodiment of the process of this invention is then run until exhaustion, which preferably occurs in 0 to about 8 to 10 minutes, but may also occur from 0 to about 30 to about 45 minutes, as described in Table 3. i The reduction in the density of the SCF-CO2 is preferably accomplished by venting or expanding the process gradually in a series of steps or in a continuous pressure reduction ramp without reducing the process temperature.

For example, the venting is preferably accomplished by removal of CO2 by steps of density, (p), i. e., Ap of 0.05 g/cm3 every 5 minutes, or by pressure drop between 15 atm to 30 atm every 5 minutes. Table 3 further characterizes depressurization by venting or expansion of the alternative process of the present invention.

TABLE 3<BR> ALTERNATIVE EMBODIMENT OF SCF-CO2 DYEING PROCESS<BR> Process Venting<BR> System Volume: 10 liters (approx.) Time (min) Pressure Temperature Density System System Change in Flow Rat (psig) (approx.) (g/cm3) Mass (kg) Mass (lb) Mass (lb) (lb/min) (°C) 0 4500 110 0.62 6.2 13.64 - - 5 4265 110 0.58 5.8 12.76 0.88 0.176 10 3962 112 0.55 5.5 12.10 0.66 0.132 15 3720 113 0.50 5.0 11.00 1.10 0.22 20 3198 113 0.45 4.5 9.90 1.10 0.22 25 3061 114 0.40 4.0 8.80 1.10 0.22 30 2776 114 0.35 3.5 7.70 1.10 0.22 35 2242 114 0.30 3.0 6.60 1.10 0.22

The temperature of the alternative embodiment of the process of the present invention may then optionally be reduced to clear the bath according to the temperature reduction step described above in Example 1 to a temperature that is still within the dyeing range, i. e., remains above the dyeing temperature (glass transition temperature of the hydrophobic textile fiber in SCF-CO2). Insolubilization of the colorant material, and subsequent precipitation of the dye onto the article to be dyed, is thereby accomplished.

Thus, in accordance with the present invention, depending on the solubility and affinity characteristics of the colorant material, the dyeing process may either be cooled without venting and then vented to atmospheric pressure or vented without cooling and then cooled and vented to atmospheric pressure.

The cooling/venting step or venting/cooling step causes most of the dye remaining in solution in the SCF-CO2 to exhaust into the polyester fiber. In the case that the venting/cooling process is required rather than the cooling/venting process, the operations are the same as for the cooling/venting process set forth in Example 1 above with respect to the preferred embodiment, but are simply reversed.

Example 3-Temperature Control Profile The solubility behavior of dyes in SCF-CO2 is a factor in the levelness of dyed textile materials. To date, prior art SCF-CO2 dyeing processes have sought to maximize the amount of dye in solution at all times. Such an approach is not necessarily the optimum in terms of achieving a level dyeing in the minimum time. Indeed, another approach involves careful control of

SCF-C02 density and temperature or use of a dye specific dosing strategy so that dye concentration at all times is favorable to rapid equilibrium for dye uptake by the fiber. Under these circumstances, unlevel dyeing problems, such as shading and streaking, are minimized. Additionally, less time at dyeing temperatures will be required to correct such problems. Such an approach is described herein.

Thus, the supercritical fluid SCF-CO2 dyeing processes of the present invention can further comprise initiating the respective dyeing processes according to a predetermined temperature control profile. While the processes described in Examples 1 and 2 above produce high quality and improved dyeings of hydrophobic textile materials as compared to prior art processes, initiating the dyeing process according to a selected temperature profile improves levelness of the dyeings and contributes significantly to a reduction in the costs associated with the production of commercial scale dyeing systems.

According to an exemplary predetermined temperature control profile, the dyeing system is set to a temperature which is below the T9 of the hydrophobic textile fiber to be dyed. For example, the temperature can be set to about 40°C. Then, the temperature is raised at a controlled rate from about 40°C to about 130°C or higher. Figure 6 provides a typical temperature control profile for a dyeing run using the exemplary dye Cl Disperse Blue 77 in SCF- CO2. The rate of temperature rise on the y-axis plot is about 1°C/minute to about 1.5°C/minute. During this time the pressure rises from about 2700 pounds per square inch (PSI) to about 4500 PSI, during which the CO2 density

is held constant. For example, CO, density is held constant at about 0.55 g/cm3, and the solublization of the disperse dye in SCF-CO2 increases as temperature increases.

Although applicants do not wish to be bound to any particular theory of the invention, it is believed that this profile promotes initial level sorption and leads to a more level dye for two reasons. Firstly, the dye is less soluble at low temperature and therefore the initial dyeing strike rate (kinetic mass transfer velocity) is slower, which avoids concentration gradients in the hydrophobic textile fiber package to be dyed. Secondly, the polyester T9 is not exceeded, which reduces the kinetic absorption rate constant and thus limits the rate of dye uptake.

By way of elaboration, introduction of the dye at lower process temperature substantially reduces both the strike rate and affinity of the dye for the fiber and typically results in lower dye concentration in the CO2. These conditions cause the colorant material to go on the fiber more slowly and to reach an equilibrium value for concentration in the fiber that is lower than that which results when the dye is introduced to the fiber at a high process temperature, such as 110°C. Moreover, since dye introduction continues with progressive increase in process temperature, conditions remain favorable during the process to maximize dye equilibrium throughout the fiber package to be dyed. Levelness is thus enhanced, and any risk of shading or streaking is minimized.

Further, with the increase in process temperature, the desorption ra' constant will increase relative to the absorption rate constant.

characteristic favors increased removal of dye from sites within the fiber package with darker shade and transport to sites within the fiber package with lighter shade, thereby leveling the package. Additionally, introduction of the dye at a lower process temperature increases the amount of time that the fiber encounters dye within the process (i. e. dyeing time), which also improves package levelness.

Thus, the slower exhaust of the SCF-CO2 dye bath results in better levelness. The complete dyeing cycle achieves a dye uptake of about 99%, and takes the heat-up time plus 30 minutes (running at 130°C) with reverse flows, 2 (I) times 2.5 (O), at 1 to 6 gpm per lb of yarn. Although applicants do not wish to be bound by any particular theory of operation, it appears that the ratio of temperature rise and dyeing temperature affect the levelness of dyeing.

A lower rate of temperature rise (start from about 40°C to about 130°C) favors more even uptake of dye before sorption equilibrium is set up.

As a consequence of the extended heating time, the dyeing cycle time increases as compared to the embodiment presented above, which also benefits levelness. Furthermore, a higher temperature of dyeing (e. g. 130°C or higher) increases migration/diffusion of dye from inside and outside to the middle of the hydrophobic textile fiber package to be dyed. Dyeing will also be level either in terms of rate of uptake or in terms of extent of uptake, i. e."kinetic or thermodynamic"terms.

Deeper dyeing and less dye shading and streaking at a dyeing temperature of t=130°C, which is far above the Tg for hydrophobic textile fiber in SCF-CO2, have been observed. Further, when using the temperature profile

according to the present invention, the dyeing machine is almost completely clean, i. e. there is little dye residue remaining in the machine after the dyeing process is completed. The increase in levelness of the dyed package may allow for the use of lower flow rates (e. g. 1 to 6 GPM per Ib. of yarn as opposed to 20 GPM per Ib. as described above) with associated economic benefits in the cost of machinery. Thus, through the use of a temperature profile as described herein, costs associated with the production of a commercial scale SCF-CO2 dye machine may be substantially reduced.

TABLE 4-LEGEND FOR FIGURES 1 AND 2 Item No. Name 10 Supercritical CO2 Dyeing System 12 C02 Supply Cylinder 14 Line Section 16 Pressure Regulating Valve 18 Pressure Indicator 20 Pressure Alarm 22 Pressure Relief Valve 24Needle Valve 26 Condenser (Shell-in-Tube Heat Exchanger) 28 Chiller 30 Turbine Flow Meter 32 Temperature Element (Indicator) 34 System Pressurization Pump (Positive Displacement) 36 Pressure Control Valve 38 Static Mixer 40 Electric Preheater __

42 Temperature Alarm 44 Over-Temperature Switch 46 Needle Valve 50 Co-Solvent Pump (Positive Displacement) 52 Needle Valve 54 Needle Valve 56 Check Valve 58 Rupture Disk 60 Temperature Element (Indicator) 62 Temperature Controller 64 Needle Valve 66 Needle Valve 68 Check Valve 70Dye-Add Vessel 71 Dye-Add Vessel Jacket 72 Temperature Element (Indicator) 74 Temperature Alarm 76 Temperature Controller 78 Control Valve (Temperature-Controlled) 80 Control Valve (Temperature-Controlled) 82 Control Valve (Temperature-Controlled) 84 Control Valve (Temperature-Controlled) 86 Rupture Disk 88 Pressure Indicator 90 Pressure Alarm 91 Line Section 92 Ball Valve (2-Way) 93 Ball Valve 9494Ball Valve (2-Way)

96 Sight Glass 98 Circulation Pump (Centrifugai) 100 Rupture Disk 102 Ball Valve (2-Way) 104 Ball Valve (2-Way) 106 Dyeing Vessel 107 Dyeing Vessel Jacket 108 Line Section 109 Needle Valve 110 Pressure Indicator 114 Ball Valve (2-Way) 116 Ball Valve (2-Way) ; 118 Coriolis Flow Meter 120120Ball Valve (3-Way) 122 Temperature Eiement (Indicator) 124 Temperature Alarm 126 Temperature Controller 128 Pressure Indicator 130 Pressure Alarm 132 Control Valve (Temperature-Controlled) 134 Control Valve (Temperature-Controlled) 136 Control Valve (Temperature-Controlled) 138 Control Valve (Temperature-Controlled) 140 Rupture Disk 142Needle Valve 144 Needle Valve 146 Line Section 148 Needle Valve 150150Temperature Element (Indicator)

152 Needle Valve 154 Pressure Control Valve 156 Separator Vessel 158 Pressure Indicator 160 Pressure Alarm 162 Temperature Element (Indicator) 164 Rupture Disk 166 Pressure Control Valve 168 Needle Valve 170 Needle Valve 172 Filter 174 Filter 176 Pressure Relief Valve 178 Check Valve 180 Line Section 182 Check Valve 184Line Section It will be understood that various details of the invention may be changed without departing from the scope of the invention. Furthermore, the foregoing description is for the purpose of illustration only, and not for the purpose of limitation--the invention being defined by the claims.