几种聚酯超细纤维染色用分散染料染色性能的研究

选用4只分散染料对聚酯超细纤维进行染色,并对其移染性、皂洗牢度及染料的高温分散性进行了研究。结果表明:染料的移染性与染料分子结构有关,分子量小,移染性好;皂洗牢度与染浴浓度有关,在相同条件下,染色浓度为4%时比12%高1级。碱性染色结果表明:BlueUP—GF在碱性条件下酯基水解严重,不适合碱性染色。     

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.     

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     

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.     

Solubility of Two Disperse Dyes Derived from <Emphasis Type="Italic">N</Emphasis>-Alkyl and <Emphasis Type="Italic">N</Emphasis>-Carboxylic Acid Naphthalimides in the Presence of Gemini Cationic Surfactants

The solubility of naphthalimide-based monoazo dyes containing N-ethyl and N-ethanoic acid groups was investigated in the presence of a conventional monomeric counterpart (DTAB) and two cationic gemini surfactants (12-4-12 or 14-4-14) individually. The effective parameters on dye solubility such as temperature, time and concentration of surfactants were investigated by UV–Visible spectrophotometry. The results demonstrate that the solubility of both dyes was considerably increased at concentrations above the surfactant CMC. The wavelength for the maximum absorbance of dyes in the aqueous solution shifts toward longer wavelengths with changes in the concentration of the cationic surfactants. A kinetic study of solubilization of dyes in cationic surfactants solution showed that the rate of solubilization follows the pseudo-first-order reactions. Rates of solubilization were in the range of 0.5 × 10⁻³ to 6.8 × 10⁻³ min⁻¹ for both dyes. The disperse dye containing a carboxylic acid group (dye 2) has a higher solubility rate than the dye containing an alkyl group (dye 1). The type of surfactant has a very low effect on adsorption of dye 1 onto the polyester fibers, whereas changing the surfactant type from DTAB to 12-4-12 or 14-4-14 causes adsorption of dye 2 on polyester to decrease.     

Dyeing kinetics of methacrylic acid grafted polyester fabric with astrazonrot violet and rhodamine red basic dyes

The low‐temperature dyeing kinetics of radiation‐grafted poly(ethylene terephthalate) fabric were studied. The effects of the graft yield (GY), dye concentration, and dyeing temperature on the color difference (CD) of methacrylic acid grafted polyester fabric were studied for astrazonrot violet (AV) and rhodamine red (RR) basic dyes. CD increased sharply with an increase in GY and tended to level off at higher degrees of grafting. The best dyeing conditions were achieved for both dyes at pH 11.5. CD of the grafted fabric increased rapidly as the dyeing time increased; this was followed by a relatively slow dyeing rate within a few minutes, which depended on the concentration and temperature of the dye bath. The initial dyeing rates and rate constants for the AV dye were higher than those for the RR dye. The dyeing process followed 0.14‐order kinetics and was independent of the dyeing temperature or the type of dye. The dyeing rates and rate constants increased with an increase in the dyeing temperature. An Arrhenius‐type plot of the natural logarithm of the dyeing rate constant versus the inverse of the absolute temperature yielded apparent activation energies of 4.9 and 13.8 kJ/mol and pre‐exponential rate constants of 9.4 and 100.6 (CD/GY)s^?1 for the AV and RR dyes, respectively. The mechanism of the dyeing process for the two dyes was diffusion‐controlled, and their dyeing rates depended on the type of basic dye. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 1070–1076, 2004     

Grafting onto polyester fibers. III. Electrokinetic properties of acrylic acid and acrylonitrile-grafted polyester fibers in the presence of cationic dyes

The electrokinetic properties such as zeta potential, surface charge density, and surface conductivity of polyester fibers grafted with acrylic acid and acrylonitrile were measured when cationic dye solutions were streamed through. The presence of the cationic dyes on the surface of the fibers and their specific adsorption at the carboxylic groups in the acrylic acid graft copolymer produce lowering of zeta potential. The decrease in surface charge density as the percent graft increases is due to the decrease in surface area of the fibers due to the adsorption of the cationic dyes. The same trend is observed with acrylonitrile-grafted fibers. The surface conductivity of the acrylonitrile-grafted polyester fibers increases with increase in dye concentration of the streaming solution. The results for the 27.4% grafted sample differed from those of the 7.32% and 12.1% grafts, which is indicative of the formation of a three-dimensional network causing change in both the physical structure as well as the chemical nature of the surface of the substrate.     

Carrier Dyeing of Polyester Fibre Part II – The Influence of Carriers on the Diffusion of Disperse Dyes

The influence of carriers on the diffusion of disperse dyes in polyester fibre has been studied. The extent to which the diffusion rate of a dye is increased is independent of the chemical structure of the carrier but depends on the molar concentration of carrier in the fibre and on the chemical structure of the dye. The influence on the diffusion rate decreases with increase in temperature, and the rates of decrease increase with increase in the activation energies of diffusion of the dyes when no carrier is present. The presence of carrier reduces the activation energies of diffusion of the dyes, the reduction being related to the decrease in the entropies of activation of diffusion brought about by the plasticizing action of the carrier. This reduction in the activation energy of diffusion leads to the existence of a temperature at which the presence of carrier would have no effect on the diffusion coefficient of the dye, and above which the presence of carrier would actually reduce the diffusion coefficient. The value of this temperature depends upon the carrier concentration in the fibre and the specific dye.     

Studies in dyeing. II. Effect of crystal modification of disperse dyes on polyester dyeing at 130°C

Four commercial disperse dyes were purified and their different crystal forms were prepared by crystallizing from different solvents or precipitating from their solutions in glacial acetic acid by dilution with water. These forms were found to have different melting points. They were dyed on polyester fibers at 130°C to fiber saturation values by changing the dyebath every 15 min. The effect of pretreatment of the dyes in an aqueous environment at different temperatures (60°, 100°, and 130°C) for 15–60 min in the presence and absence of a dispersing agent on the dye uptake values was also studied. Such treatments are shown to reduce the dye uptake. The implication of these treatments in practical dyeing are pointed out.     

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.     

The effect of heat setting on the dyeability of differentially dyeable polyester fibres

Apparent diffusion coefficients of two disperse dyes for so-called easily dyeable/cationic-dyeable polyester (ED-CDPET) and cationic-dyeable polyester (CDPET) fibres of identical linear density and sulphonic acid group content have been calculated. It was found that the diffusion coefficients of dyes for ED-CDPET were far greater than those of dyes for CDPET. The dyeability at the boil without carrier, using disperse and cationic dyes on various ED-CDPET and CDPET fibres, has been studied. ED-CDPET was found to have higher dyeability at all levels of heat setting (irrespective of the dye used). The finest ED-CDPET fibres showed maximum dye uptake as a result of increased surface area. Heat setting in the taut condition reduced dye uptake.     

Disperse dyeing of polyester fibers: Kinetic and equilibrium study

The effect of temperature on the dyeing rate constant k, diffusion coefficient D, and time of half‐dyeing t_1/2 was evaluated for the dyeing of polyester fibers with two disperse dyes, an azo and an anthraquinone dye. Activation energies of diffusion E were calculated. The polyester dyeing equilibrium was also studied and the partition coefficient K and standard affinity Δμ° at various temperatures were determined for the anthraquinone dye. Standard enthalpy ΔH° and standard entropy ΔS° of dyeing were also obtained. The same equilibrium parameters were not obtained for the azo dye because of its dyeing behavior. A similar kinetic and equilibrium study was made for the pure azo and anthraquinone compounds free from the dispersing agents present in the commercial dyes and the results are discussed. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 123–128, 2002     

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.     

Flame retardant polyesters. III. Fibers

Most of the commercial flame retardant (FR) polyester fibers are produced using copolymerization with phosphorous FRs. We investigated the fiber properties, dyeing properties, and flame retardancy according to the phosphorous FR type. The physical properties of both the fibers are similar and suitable for textile application. But the dye adsorption rate is much faster in the case of main chain type. This is resulted from higher chain mobility analyzed by glass transition temperature. The main chain type FR polyester fiber adsorbed the dyestuff at lower temperature and reached exhaustion more quickly. And the resistance to chemicals such as acidic and alkaline solutions at high temperature have similar tendency with dye absorption. The migration of dyestuffs and chemicals into the polymer chain has good correlation with chain mobility of the polymers. The main chain type polyester fiber shows better flame retardancy than pendant type polyester, which might be brought about from more rapid degradation into polyphosphoric acid. The main chain type polyester fiber shows better flame retardancy than pendant type polyester. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

The effect of dyes and dyeing on the mechanical properties of polymeric materials

The effect of reactive and disperse dyes and dyeing on the mechanical properties of cotton and polyester fibers, respectively, has been studied. It is observed that reactive dye (Procion Brilliant Red MX-2B) and disperse dye (Dispersol Red B-2B) caused a decrease in the tensile strength of the fiber which was often accompained by a decrease in the extensibility and general improvement in the tensile stiffness of the fibers. A linear relationship exists between percent disperse dye on the fiber and the square root of time of dyeing for poly(ethylene terephthalate) fibers in the initial region of dye uptake.     

Dyeing fine denier polypropylene fibers with phenylazo- &#946; -naphthol-containing sulfonamide disperse dyes

A series of phenylazo-β-naphthol-containing sulfonamide disperse dyes were prepared from C.I. Acid Orange 7 by successive reactions of chlorination and amination, and their chemical structures were characterized by FTIR, ¹H NMR, and mass spectrometry. The dyes were applied to coloring of knitted fabrics from fine denier polypropylene fibers by exhaust dyeing and their optimal dyeing conditions, such as dyebath pH, dyeing temperature, dyeing time, and dye concentration were investigated in detail. Then, dye exhaustion, color strength, and color fastnesses of the dyes on the fibers were assessed and summarized. In view of dye exhaustion and color strength of the sulfonamide dyes on fine denier PP fabrics, 90°C was selected as the best dyeing temperature at dye concentration below or equal to 3.0% owf. For achieving higher color strength, 130°C was the better choice when the dye concentration was above 3.0% owf. The sulfonamide dyes, especially secondary sulfonamide dyes, exhibited superior dye exhaustion and color fastnesses to washing, sublimation, and rubbing on fine denier PP fabrics in comparison to C.I. Solvent Yellow 14 bearing the same chromophore but without sulfonamide group.     

芳纶1313的超高温高压染色研究

本文采用超高温高压法对芳纶1313进行染色,分别研究了染料种类和染色温度对芳纶1313纱线染色日晒牢度、K/S值及染透性等方面影响,结果发现,分散染料所染纱线的各项染色性能都比阳离子染料和还原染料好;随染色温度升高,日晒牢度、纤维表面颜色深度及其纤维染透性都得到了不同程度的改善,而纱线的断裂强度随染色温度的升高变化不大。     

Disperse dyeing of polyester fibers: Kinetic and equilibrium study

The effect of temperature on the dyeing rate constant k, diffusion coefficient D, time of half‐dyeing t_1/2 was evaluated for the dyeing of polyester fibers with two disperse dyes, an azo and an anthraquinone dye. Activation energies of diffusion E were calculated. The polyester dyeing equilibrium was also studied and the partition coefficient K and standard affinity Δμ° at various temperatures were determined for the anthraquinone dye. Standard enthalpy ΔH° and standard entropy ΔS° of dyeing were also obtained. The same equilibrium parameters were not obtained for the azo dye because of its dyeing behavior. A similar kinetic and equilibrium study was made for the pure azo and anthraquinone compounds free from the dispersing agents present in the commercial dyes and the results are discussed. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2785–2790, 2002; DOI 10.1002/app.10254     

The carrier dyeing of synthetic fibers

The mode of action of carriers in augmenting the rate of dyeing of disperse dyes with acrylic and polyester fibers is discussed in terms of the plasticizing action of the carrier. It is shown that the effectiveness of a carrier is determined by its ability to reduce the glass transition temperature of the fiber and not by the fiber swelling. The rate of dyeing as measured by the diffusion coefficient of the dye is shown to be uniquely related to the difference between the dyeing temperature and the glass transition temperature (T – T_g). In the light of these results, some aspects of carrier action in dyeing from perchlorethylene are discussed. Treatment of polyester fibers with carrier also increases crystallinity. Changes in diffusion for a series of copolyesters have been correlated with the long spacing obtained from small angle X-ray scattering (SAXS).     

Dyeing fine denier polypropylene fibers with phenylazo-<Emphasis Type="Italic">β</Emphasis>-naphthol-containing sulfonamide disperse dyes

A series of phenylazo-β-naphthol-containing sulfonamide disperse dyes were prepared from C.I. Acid Orange 7 by successive reactions of chlorination and amination, and their chemical structures were characterized by FTIR, ¹H NMR, and mass spectrometry. The dyes were applied to coloring of knitted fabrics from fine denier polypropylene fibers by exhaust dyeing and their optimal dyeing conditions, such as dyebath pH, dyeing temperature, dyeing time, and dye concentration were investigated in detail. Then, dye exhaustion, color strength, and color fastnesses of the dyes on the fibers were assessed and summarized. In view of dye exhaustion and color strength of the sulfonamide dyes on fine denier PP fabrics, 90°C was selected as the best dyeing temperature at dye concentration below or equal to 3.0% owf. For achieving higher color strength, 130°C was the better choice when the dye concentration was above 3.0% owf. The sulfonamide dyes, especially secondary sulfonamide dyes, exhibited superior dye exhaustion and color fastnesses to washing, sublimation, and rubbing on fine denier PP fabrics in comparison to C.I. Solvent Yellow 14 bearing the same chromophore but without sulfonamide group.