Neutral dyeing of wool and wool/polyester blend fabrics using sulphatoethylsulphone reactive‐disperse dyes

Two models of temporarily anionic sulphatoethylsulphone reactive disperse dyes were applied to wool, polyester and wool/polyester blend fabrics at different dyeing pH. Maximum exhaustion values and colour yield were observed at pH 7. The results showed that reactive disperse dyes containing bis‐sulphatoethylsulphone reactive groups were more convenient for neutral dyeing of wool and wool/polyester blend fabrics if compared with a dye containing a mono‐sulphatoethylsulphone group. Excellent to very good wet fastness properties on all dyed fabrics were achieved.     

Effect of Sandospace R on the dyeability of gamma-irradiated wool,wool/polyester and polyester fabrics with some disperse dyes containing amino groups

The effect of Sandospace R on the dyeability of gamma-irradiated wool, wool/polyester and polyester fabrics towards disperse dyes has been investigated. The effects of the different factors that may affect the colour yield of the dyed samples (such as radiation dose, Sandospace R concentration, pH strength of the dye bath, dye concentration, dyeing temperature and time were studied. In general, and regardless of the studied factor, the irradiated fabric showed a significant dye affinity for the disperse dyes employed compared/to the unirradiated fabrics. However, the different fabrics irradiated to a dose of 2Mrad showed the highest colour strength with a high level of dyeing. Also, it was observed that a concentration of Sandospace R as low as 0·5% effectively enhances the dye affinity for the disperse dyes used here. Moreover, it was found that the pH of the dyeing bath at which the highest colour strength obtained was 3. Increasing the dye concentration up to 4% based on fabric weight, caused a significant enhancement in the colour strength, whilst raising/the dyeing bath temperature from 60°C to 100°C appreciably accelerated the rate of dye uptake. Complete exhaustion absorption of the disperse dye occurred over a period of 2h. © 1998 Society of Chemical Industry     

Application of sodium benzoyl thiosulphate from aqueous solution to wool and its effect on substantivity of disperse dyes. Part 1: synthesis and characterisation of sodium benzoyl thiosulphate

The introduction of bulky aryl residues into wool fibres not only enhances their disperse dyeability but also improves their settability, shrink resistance and imparts easy‐care properties. It would be highly desirable for colourists to achieve such effects when dyeing or printing wool from an aqueous solution as wool/polyester blend fabrics could be dyed and printed with the same dye; furthermore, in the case of an all‐wool fabric pretreated with such arylating systems, following dyeing or printing with disperse dyes, dye fixation can be achieved by dry heat procedures. A water‐soluble, fibre‐reactive arylating agent, sodium benzoyl thiosulphate, was therefore synthesised, characterised and its stability to hydrolysis in aqueous media was examined.     

One‐bath union dyeing of wool/polytrimethylene terephthalate blends†

The one‐bath dyeing of blends of polytrimethylene terephthalate (PTT) staple and wool has been investigated. The exhaustion of selected Terasil disperse dyes on PTT fibre and Lanasol reactive dyes on wool was measured as a function of temperature, together with the cross‐staining of the Terasil dyes on the wool component and the Lanasol dyes on PTT component. Most Terasil disperse dyes achieved satisfactory dye uptake on PTT at 110 °C, whereas on conventional polyester (polyethylene terephthalate) temperatures of up to 130 °C are required. An optimised union‐dyeing technique for wool/PTT blends was developed which minimised the staining of Terasil disperse dyes on wool and produced dyed goods with high levels of wet colour fastness. Carriers were not required to enhance the dyeability of PTT at low temperatures. The wool component appeared to be protected against damage at 110 °C by the reactive dyes. The results indicate the potential for blending PTT fibre and wool to produce fabrics that are easier to dye at lower temperatures than conventional wool/polyester blends.     

Use of a novel water-soluble arylating agent to dye wool and wool blends with disperse dyes

A series of water-soluble fibre-reactive arylating agents were synthesised and evaluated from the stand-point of improving fibre coloration with disperse dyes. In particular, the compound, sodio-2,4-dianilino-6-[4'- β -sulphatoethylsulphonylanilino]- s -triazine (FAA 200) was found to be promising; this compound could be applied in the same bath as a disperse dye at pH 5–6. Under the latter conditions this compound showed high substantivity to wool and at the boil readily underwent β -elimination of the sulphate ester residue to give the vinyl sulphone reactive group which adds on to nucleophilic sites in the fibre to form a covalent bond. Coapplication with commercially available disperse dyes gave bright, level dyeings that exhibited promising wet fastness. FAA 200 was used as an auxiliary to dye disperse dyes on both fibre components of a wool–polyester blend fabric; it was found that addition of hydrogen peroxide or sodium thiocyanate was necessary to obviate reduction of certain disperse dyes when dyeing at 120 °C.     

Enhancing the wash fastness of disperse dyes on wool with oxidants

Disperse dyes are not currently applied to wool commercially, in large part because of inadequate wash fastness, but they do have potential, especially for wool‐polyester blends. In this study, for the first time hydrogen peroxide was investigated to increase the wash fastness of disperse dyes on wool. In the absence of oxidants, 10 disperse dyes from seven classes imparted colours with a range of depths (K/S 2‐26) with wash fastness (grey scale ratings for colour change) grades of 3 to 4‐5. Hydrogen peroxide had only small effects on colours and gave only small enhancements to wash fastness, which were limited to anthraquinone, nitrodiphenylamine, disazo and coumarin dyes. The bleach activators Prestogen W and citric acid enhanced the bleaching effect of hydrogen peroxide but did not assist with raising wash fastness. Hydrogen peroxide in post‐dyeing scouring made the dyeings brighter but did not significantly enhance wash fastness. Ammonium persulphate, which was included for benchmarking with earlier studies, yellowed the wool and decomposed some dyes. This study extends the range of dye classes whose wash fastness on wool can be improved by ammonium persulphate to now include diazo, coumarin and methine, and confirms that oxidants/free radical initiators have potential for enabling the disperse dyeing of wool.     

Alkaline dyeing of polyester and polyester/cotton blend fabrics using sodium edetate

An alkaline dyeing of polyester with an alkali‐stable disperse dye, Dianix® Scarlet AD‐RG, was developed using sodium edetate as an alkaline buffering agent. The results obtained indicate the suitability of using sodium edetate for alkaline dyeing of polyester when compared with the control alkaline dyeing using Dianix AD system. Selected mono and bifunctional reactive dyes were used in combination with the alkali‐stable disperse dye for dyeing of polyester/cotton blend. Different dyeing methods for cotton and polyester/cotton blend fabrics using sodium edetate were evaluated in comparison with their respective control alkaline dyeing methods. The results of using sodium edetate in one‐bath two‐stage and two‐bath dyeing of polyester/cotton blend were comparable with that of the control dyeing method. Particularly, no change in the leveling and fastness properties was evaluated for all samples irrespective of the dyeing method. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Application of phthalimide-based alkali-clearable azo disperse dyes on polyester and polyester/cotton blends

Phthalimide-based alkali-clearable azo disperse dyes were synthesised and applied to polyester and polyester/cotton blends. These dyes have an alkali-clearable property that enables alkaline treatment to be substituted for conventional reduction clearing. Therefore, by using these dyes, it is possible to avoid generating dyehouse effluents with high BOD values and carcinogenic aromatic amines that may, in some cases, be liberated by reduction clearing. In addition, polyester/cotton blends can be dyed by a one-bath, two-step dyeing method, as alkali clearability enables the disperse and reactive dyes to be used in the same bath. The dyeing behaviour and fastness properties of these dyes have been investigated. In particular, the cross-staining of cotton was studied to estimate the suitability of the dyes synthesised for dyeing polyester/cotton blends.     

Phospholipid bilayers as vehicles of anthraquinone disperse dyes in wool dyeing

The use of multilamellar lipid vesicles as carriers of disperse dyes on wool fibres has been studied. Liposomes made from egg phosphatidylcholine containing the anthraquinone dye CI Disperse Violet 1 at different phospholipid/dye concentrations were used. The physical stability of these systems was assessed by measuring the mean vesicle size distribution of lipid vesicle suspensions after preparation and during dyeing. Kinetic aspects involving dye adsorption and bonding on untreated and chlorinated wool samples by means of the liposomes at different dye/lipid ratios were also investigated. This process led to the controlled dye exhaustion on wool, directly dependent on the relationship between the dye and lipid components, with a clear improvement in the dye-fibre bonding forces and in the dispersing efficiency, compared with conventional dispersing agents. The optimum dye exhaustion was reached for the dye/phospholipid concentrations 0.53 and 1.0 mmol/l respectively. The maximum amounts of dye bonded on untreated wool fibre were obtained for the same dye/lipid molar ratio. However, chlorinated wool samples showed a slight decrease in the total bonded dye as the chlorination level increased.     

Aftertreatment of polyester fabric dyed with temporarily solubilised disperse dyes

Temporarily solubilised disperse dyes derived from aminophenyl-4-(β-sulphatoethylsulphone) are exhausted on the polyester fibre mostly in the vinylsulphone form and to a lesser extent as their hydroxyethylsulphone analogues. After dyeing, to remove the unexhausted dyes on the polyester fibre, sulphite anions were added to the dyebath. The vinylsulphone residue of the dye was attacked by the sulphite anion via an addition reaction converting the dye into a soluble derivative, which then had little affinity for the polyester fibre. The effect of sodium sulphite on the conversion of the dye was investigated using HPLC. The wash and rub fastness properties of the dyed fabric aftertreated with sodium sulphite were similar to those obtained with reduction clearing.     

Dyeing of wool with temporarily solubilised disperse dyes

Temporarily solubilised disperse dyes derived from aminophenyl-4-(β-sulphatoethylsulphone) have been applied to wool fabric without the use of a levelling agent. By virtue of their characteristic dye structure, excellent levelling properties were observed on wool fabric. Good exhaustion, fixation and fastness test values were also obtained.     

Dispersant-free dyeing of polyester with temporarily solubilised disperse dyes

In an effort to overcome some of the environmental problems associated with the use of dispersing agents, four temporarily solubilised disperse dyes had previously been synthesised and characterised for use in dispersant-free polyester dyeing. In this paper the dyeing and fastness characteristics of these dyes on polyester fabrics have been examined. It was found that the optimum pH to guarantee a moderate rate of hydrolysis was 5, which allowed temporarily solubilised disperse dyes to be successfully applied to polyester without the use of dispersants. The dyebath remained stable during the dyeing procedure. The dyes exhibited good levelling and fastness properties on polyester.     

Dyeing of natural and synthetic textiles in supercritical carbon dioxide with disperse reactive dyes

Polyester, nylon, silk and wool were dyed with disperse reactive dyes in supercritical carbon dioxide (scCO₂). The dyes were substituted with either vinylsulphone or dichlorotriazine reactive groups. Since earlier research showed that water, distributed over the scCO₂ and the textile, increased the colouration, experiments were done with the vinylsulphone dye with varying amounts of water in the dyeing vessel, to investigate if there is an optimum water concentration. The amounts were such, that no liquid water was present. The maximum colouration was obtained when both the scCO₂ and the textiles were saturated with water. At the saturation point, deep colours were obtained with the vinylsulphone dye for polyester, nylon, silk and wool, with fixation percentages between 70 and 92% when the dyeing time was 2 h. The positive effect of water was due to its ability to swell fibres or due to an effect of water on the reactivity of the dye–fibre system. Also the dichlorotriazine dye showed more colouration when the scCO₂ was moist. With this dye, experiments were conducted in water-saturated scCO₂, varying the pressure from 225 to 278 bar and the temperature from 100 to 116 °C. The colouration of polyester increased with pressure, the results for silk and wool were not sensitive to pressure. Increasing the temperature had no influence on the dyeing of polyester, silk and wool. The fixations on polyester, silk and wool, being between 71 and 97%, were also independent of pressure and temperature.     

Improved mechanism of polyester dyeing with disperse dyes in finite dyebath

A new sorption mechanism of polyester dyeing with disperse dyes in water is proposed. It is considered dye aggregates could not be sorbed unless they turn into single molecules. However, this theory could not explain numerous sorption phenomena: sorption continues when equilibrium dye concentration exceeds its solubility; dyeing at long liquor ratio, using microencapsulated or crystal‐modified dyes do not change concentration of single dye molecules or dye solubility, but increase sorption rate and quantity in a fixed time. We demonstrate that both single and aggregated dye molecules could be sorbed using CI Disperse Blue 56. Because of the large size and low diffusion rate, dye aggregates could temporarily block sorption channel and prevent entry of other dyes. Therefore, only using extra more dyes could get a dark colour. Series of approaches could be proposed to reduce or eliminate the sorption problems caused by aggregates using the new sorption mechanism.     

One-bath dyeing of polyester/cotton with disperse and bis-3-carboxypyridinium-s-triazine reactive dyes. Part 1: Factors limiting production of heavy shades

Over the last 20 years, selected disperse dyes and bis-3-carboxypyridinium- s -triazine reactive dyes have been widely promoted for the exhaust dyeing of polyester/cotton blends in a one-bath-one-stage ('all-in') process under neutral conditions. However, despite the time and energy savings afforded by this elegant dyeing process, there is a belief in the dyeing industry that economical production is limited to pale and medium depths of shade. In this paper, the two dye classes (disperse dyes on polyester and bis-3-carboxypyridinium- s -triazine reactive dyes on cotton) have been investigated to understand why heavy depths of shade cannot readily be obtained economically using this process.     

Studies in dyeing. I. Effect of crystal modification of disperse dyes on their dyeing behavior

Three commerical disperse dyes and a laboratory-synthesized disperse azo dye were converted to different crystal forms. These were characterized by melting point, x-ray diffractograms, and their dyeing behavior on polyester fibers. The different crystal modifications of the same dye were shown to dye polyester fibers (but not polyamide fibers) at different rates and to different fiber saturation values. An attempt has been made to explain these differences based on a thermodynamic approach. An attempt is made to apply the concept of crystal modification of disperse dyes to some of the earlier studies done on dyeing and printing of disperse dyes on polyester and secondary cellulose acetate substrates reported in the literature.     

One-bath dyeing of a polyester/cotton blend with reactive disperse dyes from 2-hydroxypyrid-6-one derivatives

A series of temporarily solubilised reactive disperse dyes based on 1-substituted derivatives of 2-hydroxypyrid-6-one were applied to a 65;35 polyester/cotton blend using a one-bath dyeing method without dispersing agent. The dyeing behaviour of these dyes on polyester and cotton fabrics, and polyester/cotton blend fabric, were studied. The colour yields of the dyes on the polyester/cotton blend were found to be highly dependent on the initial pH, optimum results being obtained at pH 5. Good levelling and good to excellent fastness properties were obtained on the blend, with the exception of lightfastness, which was moderate.     

Dyeing of polyester using micro-encapsulated disperse dyes in the absence of auxiliaries

Polyurea microcapsules were prepared in this study, using disperse dye as the core material and diphenylmethane-4,4'-diisocyanate as the wall-former. Microencapsulated disperse dyes have been characterised in terms of their thermal properties, average particle size and size distribution, morphological structure and composition. Polyester fabric was dyed with microencapsulated CI Disperse Blue 56 using a high temperature dyeing process without dispersing agents, penetrating agents, levelling agents or other auxiliaries. The quality of the polyester fabric dyed in this manner – without reduction clearing – was at least as good as that dyed traditionally after washing and reduction clearing. After separating off the polyurea microcapsules, the dyebath was virtually colourless and was shown to be suitable for reuse.     

Dyeing of Wool–Polyester Blends with Reactive Disperse Dyes: Variation of Dye Distribution and Reactivity for Wool

The dyeing behaviour of structural analogs of some commercial reactive disperse dyes on a simulated 70:30 wool–polyester blend has been studied. By varying the hydrophi/ic– hydrophobic balance of the dye molecule major changes in the distribution of dye between wool and polyester were observed. The reactivity of the γ–halo–β–hydroxypropyl group was found to be dependent on the halogen atom, while the reactivity of the N–bromoalkylsulphonamide group was found to be dependent on the position of the bromine atom.     

Diffusion of disperse dyes into super-microfibres

The disperse dyeing process for polyester fibres is complex. It is characterised by the diffusion-controlled sorption of dyes and depends on dye concentration, dyebath temperature, dye liquor flow rate and fibre count. Moreover, the dyeing properties of super-microfibres are also quite different from those of microfibres or conventional polyester fibres. In this paper the influence of dyebath temperature, initial dye concentration and fibre count on the diffusion coefficient and the sorption isotherms has been studied. The analysis of kinetic properties has been restricted to infinite dyebath conditions. All experimental results have been compared terms of fibre count and dyebath temperature.