Diffusion of dyes in polyester fibers. IV. Anomalous sorption of disperse dye synthene scarlet P3GL

The investigations on dyeing of poly(ethylene terephthalate) fibers with disperse dye Synthene Scarlet P3GL have revealed anomalous sorption of the dye in heat-treated samples. In the mathematical solution of the process it has been assumed that anomalous sorption can be treated as superposition in time of two stages of Fickian sorption. The contents of absorbed dye at quasiequilibrium C_I, at the final equilibrium C_II, and the apparent diffusion coefficients D_I, and D_II have been calculated using Hill's equation.     

Diffusion coefficients of direct dyes in chitosan

Diffusion coefficients for direct dyes (C. I. Direct Red 81, Green 26, Blue 75, and Black 22) in Chitosan films are determined to be 4.48 × 10^?11 to 4.54 × 10^?10 cm²/at 60°C and pH 9. A method for producing chitosan films is described.     

Diffusion of dyes in polyester fibers. III. Time delay in establishment of the equilibrium concentration of dye at fiber surface

In the dyeing process of the copolyester fiber Dilana with the disperse dye Synthene Scarlet P3GL, a deviation from the simple model of Fickian sorption occurs. It manifests itself as a time delay in establishment of the equilibrium dye concentration at the fiber surface. As has been stated, the variation of C_s (the surface dye concentration) with time of dyeing fits the equation; C_s = C_∞ (1? e^?βt). Regarding the relation of C_s to t, the diffusion coefficient of the dye in the studied fiber has been calculated by the theoretical equation reported in Crank's monograph. It has been proved that the experimental data on kinetics of dyeing the fiber Dilana with Synthene Scarlet P3GL fit considerably better the tested equation than the classical Hill's equation.     

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.     

Diffusion of disperse dyes into microfibres and conventional polyester fibres

The dyeing properties of polyester microfibres are quite different from those of conventional polyester fibres. In this paper, the sorption isotherms, the diffusion coefficients and the amount and rate of dye uptake into the fibres are compared for both conventional fibres and microfibres. Shibusawa's approximation of Hill's equation is used to compute the diffusion coefficient, which depends on the initial dye concentration, the time and the fibre count for a fixed temperature (130 °C). The kinetic properties are analysed only under infinite bath conditions. The sorption isotherms and diffusion coefficients as functions of time for conventional polyester fibres and microfibres are compared by considering the surface area and the diffusional boundary layer influence.     

Optothermal properties of fibers. II. Annealing effect on the birefringence variations of polyester fibers

The variation of refractive indices and birefringences of Egyptian-manufactured polyester fibers with different annealing times at constant temperature 160°C are studied by inter-ferometry. The polarizing interference microscope is used for determining the mean re-fractive indices and mean birefringence of these fibers. The results are used to calculate optical orientation function and the angle of orientation. Also, the acoustic method has been used for measuring the density and the mechanical loss factor of these fibers. Relations between the mean refractive indices, birefringence, polarizabilities, mechanical loss factors, and densities with annealing time are given for these fibers. Illustrations are given using graphs and microinterferograms. © 1996 John Wiley & Sons, Inc.     

聚酯超细纤维用分散染料染色性能的研究

该文通过对现有的分散染料染色性能测试,如,聚酯超细纤维的移染性、皂洗牢度及高温分散稳定性等,并进行了碱性染色实验,为选择适用于聚酯超细纤维染色的染料提供一定的参考依据.     

Study on the dyeing properties of hemicyanine dyes. II. Cationic dyeable polyester

The absorption spectra of two hemicyanine fluorescent dyes, namely, trans‐4‐[p‐(N,N‐di(2‐hydroxyethyl))‐amino‐styryl]‐N‐ethyl pyridinium bromide (DHEASPBr‐C₂) and trans‐4‐[p‐(N,N‐di(2‐hydroxyethyl))‐amino‐styryl]‐N‐octyl pyridinium bromide (DHEASPBr‐C₈), were studied at various levels of pH and high temperatures, and were then employed to dye cationic dyeable polyester. Their dyeing properties, fluorescent reflectance and colorimetric properties were explored. The novel fluorescent dyes existed in two forms of monocation and dication in solutions at low pH and high temperature. Overall, the influence of pH on colour depth and the maximum reflectance of dyed cationic dyeable polyester was extremely small. The adsorption mechanism of DHEASPBr‐C₂ and DHEASPBr‐C₈ on cationic dyeable polyester fibres was in good accord with the Langmuir type. Compared with DHEASPBr‐C₂, DHEASPBr‐C₈ exhibited comparatively faster adsorption rate, higher affinity and dye uptake, while its fluorescence shown by cationic dyeable polyester was slightly weak.     

Interaction of dyes used for foods with food packaging polyester fibers

The effect of pH, temperature, dye concentration, and additives on the absorption of the dyes FD & C (Food, Drugs and Cosmetics) Blue 1 and Blue 2 upon poly(ethylene terephalate) (PET) and poly(butylene terephthalate) (PBT) subjected to different draw ratios (and, thus, resulting in different percentage crystallinities determined with DSC and wide-angle X-ray diffraction patterns) was investigated and a correlation between these parameters and the dye uptake was suggested. The absorption kinetics of the dyes on the polyesters were studied and a mechanism based upon the development of hydrogen bonds between the dyes and the end groups (? COOH,? OH) of the polyesters and the swelling of the network was proposed. Finally, an indirect measurement of the T_g values of the polyesters was suggested based upon the different dyeing diffusion rates. © 1994 John Wiley & Sons, Inc.     

Grafting onto polyester fibers. II. Kinetics of grafting of acrylic acid,acrylonitrile, and vinyl acetate onto polyester fibers

The kinetics of grafting of acrylonitrile, acrylic acid, and vinyl acetate onto polyester fiber by catalytic initiation and radiation were studied. The energy of activation determined for acrylic acid grafting by the catalytic method was 10.7 kcal/mole and that for vinyl acetate grafting by the radiation method, 11.7 kcal/mole. In the case of acrylonitrile grafting by the catalytic method, the rate of grafting decreased with increase in temperature of grafting, showing the differential behavior of the precipitating type of polymer from that of homogeneous polymerization.     

Thermotropic polyester carbonates. II. Polyester carbonates as high performance fibers

The fiber spinning and heat treatments of spun fibers from thermotropic polyester carbonates are described. Thermotropic polyester carbonates derived from t-butylhydroquinone, methylhy-droquinone, diphenyl terephthalate, and diphenyl carbonate in the molar ratios of 50 : 50 : 55 : 45; 50 : 50 : 57.5 : 42.5; can be spun successfully, and after proper heat treatment, yield fibers with tenacity as high as 20 g/denier. Normally the best spinning temperature is 10–20°C above melting.     

Diffusion with simultaneous reaction of reactive dyes in cellulose. II. Effect of hydrolysis

Theoretical equations that describe the concentration profiles of immobilized and active species for reactive dyes were derived from the diffusion equation accompanied by the reaction with cellulose and water in the substrate. The diffusion coefficient D and the rate constant of the reaction with cellulose, k_cell, and that with water in cellulose, k_w, were estimated by using the theoretical equations and the cylindrical film roll method. The theory predicted that the apparent diffusion coefficients decreased with the hydrolysis of active species in cellulose. Results from diffusion experiments with C.I. Reactive Yellow 4 and Orange 1 show that the ratio P of k_w to k_cell for Orange 1 increased with increase in pH to about pH 13 and that the P for Yellow 4 was smaller than unity. Using an alternative experiment to diffusion, P of Orange 1 was measured to be 1.0–1.5, and that of Yellow 4 was smaller than unity at pH 11.6 at 30°C. It was therefore concluded that the D of active species was constant to a highly alkaline region and that the decrease in the apparent diffusion coefficient of Orange 1 was mainly due to the hydrolysis of active species in cellulose.     

Grafting onto polyester fibers. IV. Synergism during graft copolymerization of binary mixtures of vinyl monomers onto polyester fibers

Graft-copolymerization reactions of binary mixtures of vinyl monomers (acrylamide–acrylic acid and acrylonitrile–acrylic acid) with polyester fibers have been studied by chemical initiation technique using benzoyl peroxide as an initiator. The total graft add-on was determined gravimetrically, while the modified Kjeldahl's method for N-estimation was employed to determine acrylamide and acrylonitrile grafts in their mixtures with acrylic acid grafts. Synergism of very high order was noticed during the graft-copolymerization reactions. In the case of the acrylamide–acrylic acid system a very high order of synergism (129.15%) was noticed at equimolar proportions of the monomers in the grafting bath. Both acrylamide and acrylic acid showed synergistic influence over each other during graft-copolymerization reactions. In the case of the acrylonitrile–acrylic acid system, however, the presence of acrylonitrile reduced the graft yield of the acrylic acid component showing a negative synergism; but acrylic acid enhanced the acrylonitrile graft yield to a considerable extent. The results have been explained in terms of reactivity ratios of the monomers. The conductivity results of the monomer mixtures also supported the experimental results.     

Diffusion of dyes in natural fibres

This review provides a summary of research on the penetration of dyes into natural fibres. Emphasis is placed on the relationship between diffusion and the structural morphology of the fibres. The types of commonly dyed natural fibres, the methods of measurement of diffusion and the data that have been collected by the use of each method are reviewed. The applicability of general theories of dyeing to natural fibres is also examined. Recent developments that have led to the direct observation of penetration pathways in wool fibres are described, together with the insights obtained into diffusion phenomena. Areas for future work are briefly indicated.     

Diffusion of dyes in adsorptive dyeing

The concentration dependence derived from both steady-state permeation and unsteady-state dyeing runs for a system of acid dye C. I. Acid Blue 182-nylon 6 film was analyzed in terms of parallel diffusion with simultaneous multimodal adsorption proposed in the previous paper. The present dyeing process was governed by the surface diffusion incorporating three kinds of Langmuirean adsorption modes. The concentration dependence of the diffusion coefficient of the cationic dye C. I. Basic Red 22 in the anionically modified polyester fiber Dilana measured by Ostrowska et al. [B. Ostrowska, A. Narebska, and H. Krzystek, J. Appl. Polym. Sci., 26 , 463 (1981)] was satisfactorily interpreted by the parallel diffusion incorporating two kinds of Langmuirean adsorption modes.     

Optothermal properties of fibers. VIII. Structure orientation study of annealed Egyptian polyester fibers

A two-beam interferometric method is used to study the change of optical orientation functions and the molecular structure of annealed Egyptian poly(ethylene terephthalate) (PET) fibers. The acoustic method was used for measuring the density. The density results were used to calculate the degree of crystallinity of PET. It was found that annealing causes alignment to the fiber chains in the directions of the fiber axis. This alignment gives an increase in the optical orientation function and decrease in orientation angle. The value of Δα/3α₀, which depends upon the molecular structure of the polymer, remains constant. The obtained results of the optical and the density clarify that new reorientations occurred due to annealing at different conditions. The changes of the refractive index profile of annealed PET fibers are given. Microinterferograms and curves are given for illustration. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 65: 2031–2050, 1997     

Cure of polyester resins. II

The copolymerization reaction between unsaturated polyesters and styrene has been studied by a torsional pendulum. The accuracy of the dynamic-mechanical measurements obtained is discussed briefly, and the results are compared with those of previous work on the change of hardness during cure.     

One-bath dyeing of wool/polyester blends with acid and disperse dyes. Part 2 — disperse dye distribution on polyester and wool

Disperse dye distribution on polyester and wool during one-bath dyeing of wool/polyester blends is discussed. The addition of carriers increases the wool's intrinsic saturation value for disperse dye, thus raising the degree of staining on the wool component at the low dye uptakes. However, staining can be minimised if the dyeing is close to or attains equilibrium conditions. Sequestering agents can accelerate the disperse dye diffusion out of the wool fibre, further reducing staining on wool and transferring more disperse dyes from wool to polyester. Citric acid can be used as a sequestering agent as well as a pH adjusting agent.     

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.     

The accessibility of sulphonic acid groups in basic dyeable polyester fibers. II. The influence of plasticization on the ion exchange process

The exchange of the sodium ions of the sodium sulphonate group in anionically modified polyester fibers has been measured. The accessibility of the sulphonate groups in the polymer is greatly improved by plasticization and is independent of the size of the exchanging ion.