Synthesis and Structure Properties of Flame Retardant and Cationic Dyeable Polyamide 6 Modified with 5-sulfoisophthalic Acid Sodium and Melamine Cyanurate

Unmodified polyamide 6 commonly dyed with acid dyes, and has no flame-retarded properties. So they are flammable and can be easily stained by foods or drinks that contain acid dyes. However, the acid groups react with amino groups that existed at the end of PA6 chain while using cationic dyes. Thus, the acid dyes can be washed immediately. In this study, the flame retardant and cationic dyeable polyamide 6 (FRCD-PA6) modified with 5-sulfoisophthalic acid sodium (5-SSIPA) and melamine cyanurate (MCA) was successfully prepared by the two-step-melt polymerization method. Firstly, cationic dyeable polyamide 6 (CD-PA6) was prepared with sodium salt from 5-sulfoisphthalic acid. Secondly, melamine cyanurate, as an efficient flame retardant, was blended into the reaction. The chemical and crystalline structures of FRCDPA6 were characterized by the Fourier transform infrared spectroscopy (FT-IR) and wide angle X-ray diffraction (XRD). Their thermal properties were tested by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA), and morphology was analyzed by SEM, respectively. It had been measured to prove the dispersion of 5-SSIPA and MCA on polyamide 6 matrix. Incorporating with 5-SSIPA created more amorphous regions and rose up the dyeing rate easily, with a highest dyeing rate for about 96.79 %. The effect of varying MCA content on the composites showed more flame retardant and made better heat-resistance. Moreover, with the appropriate addition of MCA content, the limit oxygen index (LOI) reached up to 27, less smoking, no more black smoke, droplet phenomenon was slightly, and flame resistance had greatly improved. Because of the good synergy between 5-SSIPA and MCA, a kind of novel modified polyamide 6 which own both cationic dyeable and efficient flame retardant properties was born.     

Dyeing of synthetic fabrics in water using azoic dyes based on boronic acid derivatives

Development of water-soluble dyes for the dyeing of different textile fabrics is essential for the textile industry due to ecological and economical reasons. In this study, a series of new azoic dyes were prepared by diazotization reaction between the phenyl boronic acid and different aniline derivatives, and their dyeing capacity in aqueous solution was evaluated. The synthesized boronic azo dyes present good water solubility and can dye polyamide (nylon), wool, silk, and cellulose acetate fabrics. The effect of factors such as concentration of dye, dyeing temperature, and pH on the level of color strength (K/S) was studied. The dyeing results showed that higher color strength K/S (about 16) and fastness properties (about 4/5) with boronic acid dyes were achieved at higher temperatures avoiding the use of surface agents, mordants, and other polluting chemical additives.     

Design,characterization, dyeing properties,and application of acid-dyeable polyurethane in the manufacture of microfiber synthetic leather

The difficulty in dyeing microfiber synthetic leather filled with ordinary polyurethane presents a significant challenge in maintaining the uniformity and highly realistic appearance of the resulting products. In the present study, a type of acid-dyeable polyurethane (PU-MDEA; MDEA=N-methyldiethanolamine) was synthesized, and its chemical structure and dyeing properties were investigated. Nuclear magnetic resonance analysis indicated that cationic groups were successfully incorporated into the PU-MDEA backbone via chain extension using MDEA. The amorphous nature of PU-MDEA was determined by differential scanning calorimetry, X-ray diffraction, and polarizing optical microscopy. Owing to the strong binding between these cationic groups and acid dye, as well as the reduced resistance to dye penetration, PU-MDEA showed better dyeability toward the acid dyes studied herein when compared with the control sample (microfiber synthetic leather filled with ordinary polyurethane). The adsorption isotherm experiment revealed that the dyeing process conformed to the Langmuir model, thereby indicating that the acid dyes attached to PU-MDEA via strong ionic bonding rather than van der Waals forces or hydrogen bonding. Additionally, it was found that the wastewater resulting from the dyeing of the microfiber synthetic leather filled with PU-MDEA exhibited environmentally friendly characteristics when compared with that displayed by the control sample (microfiber synthetic leather filled with ordinary polyurethane). Thus, the current results show the potential of PU-MDEA, as a filler, in the manufacture of microfiber synthetic leather to achieve fast dyeing rate, high dye uptake, and good color fastness, thereby improving the uniformity and highly realistic appearance of the resulting products.     

Application of triazole-containing gemini cationic darkening agent in cold pad batch dyeing for cotton knits

4-Amino-double(octadecyldimethyl ammonium chloride)-1,2,4-triazole (ADAC-TZ), a gemini cationic auxiliary with a heterocyclic triazole structure, was designed and synthesized by the method described here and characterized for use in the cold pad batch dyeing of cotton knits. The results show that, for ADAC-TZ, the critical micelle concentration (CMC) is 4.0×10^-4 mol/l, the Krafft point is 29.8 °C, the foam height is only 169 mm/5 min, and the solubilization for toluene is 6.67 ml/g, which means that ADAC-TZ exhibits excellent low-foaming, water solubility and solubilization properties. The present research also demonstrates that ADAC-TZ pretreatment can increase the K/S value, dye fixation, and color fastness to washing and rubbing of cotton knits dyed through BES reactive dye cold pad batch dyeing used in combination with the alkaline agent QF-4.     

High Light-Fastness Acid Dyes Synthesized from Corresponding Anthraquinone Chromophore Utilizing a Sulfonation Reaction. I. Dye Synthesis and Characterization

As the diameter of polyamide fibers decreased to finer denier, the dyeing fastness tends to be deteriorated due to the increase of their surface area, particularly both light fastness and wash fastness. In this study, three acid dyes were synthesized utilizing a sulfonation reaction starting from corresponding hydrophobic dye (for yellow and red dye) and dye intermediate containing a sulfonic acid group (for blue dye), those featured by high light fastness property. A Gaussian structural prediction model was used to determine the structure of the acid dyes prior to dye synthesis, and the optimal structures of three acid dyes were analyzed. Dye structures prepared were confirmed by ¹H-NMR, mass spectroscopy, and elemental analysis. By using a UV-vis spectrophotometer, the absorption maxima and molar extinction coefficient were also measured for three acid dyes comparing to that of the corresponding disperse dye or blue dye intermediate. Judging from spectroscopic data, the introduction of sulfonyl groups led to increase of molar extinction coefficient and a bathochromic shift.     

LED-UV grafting of vinylsulfone dyes onto photo-oxidized wool fabrics

Photografting coloration of wool was carried out under UV-LED irradiation at room temperature using aqueous vinylsulfone dye solution containing vinylsulfonic acid as a comonomer. UV-LED irradiation of the 395 nm emission is more energy efficient, less damaging to the dyes, and much safer to human eyes compared with polychromatic mercury UV lamps. However, in case of the UV-LED lamps, the wool needs to be photo-oxidized either by UV/ozone or polychromatic UV irradiation before the dye photografting. The surface treatments increased the sulfur and oxygen contents in the modified wool surfaces. While the optimally photografted wool fabrics under the UV-LED lamp yielded a K/S value of 9.9, the K/S of the grafted wool increased to 25.2 and 13.6 after the UV/Ozone or polychromatic UV preoxidation at UV energies of 10.6 J/cm² and 25 J/cm² respectively. The color fastness properties of the photografted fabrics were far better than with those of the conventionally reactive-dyed fabrics, implying that the high-molecular-weight photografted dyes seemed to be more durable than the low-molecular dyes.     

Improvement of toughness for the hyaluronic acid and adipic acid dihydrazide hydrogel by PEG

New applications call for many new requirements. In order to improve the toughness of aldehyde hyaluronic acid (A-HA) and adipic acid dihydrazide (ADH) hydrogel, the poly(ethylene glycol) (PEG) was added. PEG content and molecular weight have little effect on the gelation time, and the composite hydrogels can form in situ within 20 seconds at room temperature. The press test showed that the hydrogels containing PEG possessed a better compression resistance, after pressed more than five times, the composite hydrogels could restore. Rheological properties were measured to evaluate the working ability and the effect of PEG on hydrogels. By analyzing the shear viscosity (η _γ=0.01), yield stress (σ ₀) and threshold shear stress (σ _c ), the addition of PEG can make the structure of composite hydrogels get loose and improve the shear resistance. Especially, PEG800 can enhance the antishear ability obviously. The amplitude sweep tests showed a broad linear viscoelastic region, indicating a wide processing range. In the meanwhile, we also found that PEG can improve the optical transmittance of xerogel evidently.     

Functionalization of the aquatic weed water hyacinth <Emphasis Type="Italic">Eichhornia crassipes</Emphasis> by using zinc oxide nanoparticles for removal of organic dyes effluent

In this study, purified Eichhornia crassipes dead biomass, coated biomass with ZnO nanoparticles (NPs) and one coated with both ZnO NPs and polyethylenimine (PEI) were successfully fabricated as a bioadsorbent and biodegradent of organic dyes from the textile dye effluent. These ZnO NPs are capable of enhancing the dispersability and adsorption capacity of PEI and the anionic dyes. The surface analyses of Eichhornia crassipes, Eichhornia crassipes/ZnO NPs and Eichhornia crassipes/ZnO NPs/ PEI were characterized by SEM, specific surface area and micropore volume. The effect of three parameters including Eichhornia crassipes concentration, dye concentration and contact time on the color removal percent and degradation percent were evaluated. The results showed that the bleached Eichhornia crassipes was an efficient adsorbent for cationic dyes. Also, the effectiveness of Eichhornia crassipes/ZnO NPs was employed as photocatalytic agent for the degradation of C.I. Direct Red 23 in the presence and absence of UV irradiation. Moreover, Eichhornia crassipes/ZnO NPs/PEI shows a high adsorption capacity toward the anionic dyes C.I. Acid Red 40 and C.I. Reactive Orange 91. It was found that, Eichhornia crassipes/ZnO NPs was completely degraded C.I. Direct Red 23 by >90 % within 90 min of UV irradiation time, whereas in the absence of UV irradiation it required a substantially longer time (120 min) to achieve a similar degradation percent. In addition, Eichhornia crassipes/ZnO NPs/PEI was most effective and show the maximum adsorption capacity for C.I. Reactive Orange 91 and C.I. Acid Red 40 and its efficiency for the color removal percent was 100 % for C.I. Reactive Orange 91 and 95 % for C.I. Acid Red 40 in less than 60 min processing time.     

Dyeing behavior of chemically modified poly(1,4-phenylene sulfide) fiber towards disperse,anionic, and cationic dyes

Poly(1,4-phenylene sulfide) (PPS) exhibits good dimensional stability and flame retardant characteristics but its commercial development as fibers is highly limited due to lesser dyeing and finishing characteristics. Hence in the present study, we focused on the anionic and cationic modifications of PPS to enhance its dyeing ability towards disperse, cationic, and anionic dyes. Novel sulfonation and chloromethylation-quaternization of PPS fiber were carried out to achieve an industrially viable dyeing process methodology. The chemically modified PPS fiber is dyed with disperse, cationic, and anionic dyes, and the dyeing adsorption efficiency is quantitatively studied using a dye-o-meter equipped with UV-visible absorption spectroscope. The ideal parameters for dye adsorption were determined as a function of dyeing time, material-toliquor ratio, dyeing temperature, carrier concentration, sulfonation, and chloromethylation. The fastness properties of the dyed fabrics were also studied. Overall, with a maximum dye uptake of 99 % and 90 % achieved for sulfonated PPS and quaternized PPS respectively, the optimized conditions can be readily scaled-up to the commercial dyeing of PPS fiber with disperse, anionic, and cationic dyes.     

Synthesis of hydrophilic copolyesters and the characterization of their moisture-related cooling properties

A series of copolyesters (Co-PETs) containing poly(ethylene glycol) (PEG), 5-sodiumsulfodimethyl isophthalate (DMS), and dimethyl isophthalate (DMI) were synthesized via the conventional two-step melt-polycondensation method. The synthesized Co-PETs were characterized by ¹H-NMR spectroscopy, FT-IR spectroscopy, differential scanning calorimeter (DSC), and thermogravimetric analyzer (TGA). The DSC results showed that the melting temperature (T _m) and the heats of fusion (ΔH _m) of Co-PETs decreased with increasing the DMS content in Co-PET, while the inclusion of PEG did not affect their thermal properties significantly. The water absorption and the water contact angle of the Co-PET films were found to be significantly affected by the DMS content rather than PEG content. The moisture-related cooling properties of the fabric samples made of Co-PET 5 as well as PET were evaluated by using liquid moisture management tester (MMT) and Q _max measurements. The MMT and Q _max results indicated that Co-PET 5 fabric containing DMS 1.0 mol% and PEG 10.0 wt% in Co-PET seemed to be a good candidate for the fabric having durable cooling effects.     

Dyeing properties of mixture of ultrafine nylon and polyurethane with different types of dye

The dyeing and color fastness properties of levelling type acid dye, milling type acid dye, metal complex dye and reactive dye on ultrafine nylon, polyurethane fiber/film and their mixtures were investigated. Ultrafine nylon was dyed well with four types of dye at pH 3-6, but levelling type acid dye showed low washing fastness. Amine-rich polyurethane fiber exhibited enhanced dyeability due to amino groups which acted as dyeing sites, compared to regular polyurethane fiber. In simultaneous dyeing with milling type acid dye and metal complex dye, amine-rich polyurethane fiber absorbed more dye molecules than ultrafine nylon, the color difference between two fibers were apparent. Polyurethane-impregnated ultrafine nylon was also prepared and its build-up properties were determined. It was found that polyurethane whose soft segment was composed of polytetramethylene glycol (PTMG) and polypropylene glycol (PPG) showed improved dyeing property and subsequently high color strength.     

Extraction,Dyeing, and Antibacterial Properties of <Emphasis Type="Italic">Crataegus Elbursensis</Emphasis> Fruit Natural Dye on Wool Yarn

Fruits obtained from shrubs of the Crataegus elbursensis (C. elbursensis) plant demonstrate significant antioxidant and antibacterial properties. In this study, natural dye was sono-extracted from fresh and dried fruits and applied in dyeing and antibacterial finishing of wool. The maximum sono-extraction yield was obtained when optimal conditions of ethanol/ water (4/1 v/v) as extracting solvent, time 30 min, pH 4, temperature 50 oC, and C. elbursensis concentration 10 g/l were used. When wool yarns were dyed with the extracted natural dye, the maximum dye uptake was achieved using dye concentration 75 % owf, and dyeing condition of 100 oC, 60 min, pH 4, and LR 100:1. Different metal salts like aluminum sulfate, copper sulfate, and tin chloride were applied on wool by pre-mordanting method and their effects on dye uptake, color variation, and color fastness were examined. Results showed that the natural dye itself had relatively high uptake and good color fastness on un-mordanted wool. Further, each mordant had different effect on dye uptake, color variation, and color fastness properties depending on its coordination ability with dye molecules and wool chains. Moreover, dyed yarns showed good antibacterial activity against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) bacteria.     

A study on combining natural dyes and environmentally-friendly mordant to improve color strength and ultraviolet protection of textiles

In this study, natural dyes were extracted from five plants, namely diospyros kaki, dioscorea cirrhosa, millettia (jixueteng), ecliptae, and macrocarpa nucuma, using environmentally-friendly solvents, including ethanol and deionized (DI) water. A plant mordant, tannin extracted from Emblica officinalis G., and a metal mordant, copper sulfate, were used in the pre-dyeing process. Cotton and silk fabric samples were treated using the five natural dyes without and with mordanting for comparison on their color strength and characteristics as well as protection against ultraviolet radiation (UVR). Results revealed that Emblica officinalis G. had the highest total phenol content, followed by dioscorea cirrhosa. The presence of abundant phenolic groups in the natural dyes and mordant makes them effective coloration agents for fabrics. Cotton and silk fabrics dyed using ecliptae without pre-mordanting had the highest K/S values. Silk fabrics had higher K/S values than cotton fabrics, indicating greater color strength in pre-mordanted silk treated with DI water-extracted dyes. Natural mordant used before treatment with natural dyes contribute to significant enhancement in color strength, and Emblica officinalis G. alone could darken the color of cotton and silk fabrics dyed with plant pigment. Moreover, treatment with natural dyes after mordanting can increase ultraviolet protection factor (UPF) and the enhancement in UVR protection is greater and more significant in cotton fabrics than in silk fabrics, and in fabrics treated with DI water-extracted natural dyes than in those treated with ethanol-extracted ones. In conclusion, pre-dyeing with natural mordant followed by treatment with natural dyes extracted using environmentally-friendly solvents can enhance significantly K/S and UPF, offering directions for manufacturing textiles without environmental hazards but with good appearance and health benefits.     

Synthesis and spectral characterization of novel azomethine disperse dyes derived from pyrazolone moiety and their dyeing performance on polyester fabrics

A series of new azomethine dyes based on pyrazolone system have been synthesized via different routes. The solvatochromism for the dyes was evaluated with respect to spectroscopic properties in various solvents. The dyes were applied as disperse dyes on polyester fabrics and gave shade poor to excellent light fastness, washing, perspiration, sublimation, and rubbing fastness properties. Also the position of color in CIELAB coordinates (L*, a*, b*) and K/S value were investigated.     

Synthesis,Characterization, and Dyeing Performance of Thiadiazole Derivatives

N⁴-(5-methyl-1,3,4-thiadiazol-2-yl)thiazole-2,4-diamine derivatives have been synthesized by the reaction of 2-amino-5-methyl-1,3,4-thiadiazole and chloroaecetylchloride with suitable solvent, then cyclized with thiourea at reflux temperature in methanol to yield N⁴-(5-methyl-1,3,4-thiadiazol-2-yl)thiazole-2,4-diamine which was diazotized and coupled with various naphthalene acid couplers to give new series of acid dyes (AD₁-AD₁₃). All the compounds were characterized by their percentage yield, melting point, elemental analysis, UV spectra, IR spectra, and NMR spectra and dyeing performance on nylon fabric has been assessed.     

Adsorption of Graphene Oxide onto Synthetic Fibers: Experimental Conditions

Comparative studies on the adsorption capacity of two synthetic fibers, polyamide (PA 66) and polyester (PET) pre-treated with N-cetylpyridinium chloride (PET-NCPCl), towards graphene oxide (GO) have been carried out. The fiber samples were characterized by scanning electron microscopy (FE-SEM) and Raman spectroscopy. The results of adsorption isotherms, kinetics, and zeta potential determinations as a function of the GO concentration, pH, and temperature show that at a low pH of 2.5 and a high temperature of 323 K, almost 99 % of the 75 mg/l GO solution is adsorbed onto PA 66 and 70 % onto the PET-NCPCl fibers. The interaction should be first attributed to electrostatic forces, also the adsorption data exhibited a good fit to the Freundlich isotherm model and the free energy value of 10 kJ/mol was in the range of physical adsorption, which could suggest that the interaction is driven mainly by physical forces. Due to the increasing development of wastewater treatments based on the GO reactivity with metals and cationic contaminants, synthetic fibers coated with GO could be considered an adsorbent for environmental applications.     

Cotton Dyeing and Antibacterial Finishing Using Agricultural Waste by an Eco-friendly Process Optimized by Response Surface Methodology

In this study, Berberis vulgaris L. wood as an agricultural waste was used for dyeing and functional finishing of cotton. To facilitate the attachment of natural dye, citric acid was used to create carboxylic acid functional groups on cotton fibers. The process of crosslinking of cotton fabric with citric acid was optimized in order to obtain the maximum dyeability with the cationic natural dye. The effects of three important factors including citric acid concentration, sodium hypophosphite concentration and curing temperature on the color strength of the dyed samples with woods of barberry tree were analyzed by response surface methodology and the optimum conditions for obtaining the highest color strength was obtained. The crosslinking of citric acid on cotton fibers was confirmed by FTIR spectroscopy. The dyed sample prepared under the optimum conditions of crosslinking showed good wash and light fastness properties besides very good antibacterial activity against gram-negative and gram-positive bacteria.     

Extraction of natural dye from <Emphasis Type="Italic">Coreopsis tinctoria</Emphasis> flower petals for leather dyeing − An eco-friendly approach

This study evaluated the extraction of two colors of dye (yellow and brown) from Coreopsis tinctoria flower petals using ultrasound and the dyeing of leather with the extracted dyes as a source of nontoxic and eco-friendly dye. The results showed an increase in the dye extraction values with increasing time at 100 W ultrasonic power at 80 °C for 1 h. Leather dyeing was optimized with the aid of ultrasound and magnetic stirring. The optimum leather dyeing conditions, with respect to the dye uptake, dye penetration and intensity of the color, were determined to be 12 % dye concentration, 100 W power, 1,000 rpm, and pH 7.0 for 60 min at 80 °C. It was shown that sonication improves dye exhaustion from a 90 % to 60 % rating for 1 h of dyeing time. The dyed leather was assessed by reflectance measurements and compared with visual assessment data. The fastness properties of dyed leather samples showed good fastness against washing, light, and dry and wet rubbing. The strength properties were not significantly altered and the bulk properties, such as softness, were found to be improved by the use of Coreopsis tinctoria yellow and brown dyes using an ultrasonic and magnetic stirring dyeing process.     

Combined use of cationization and mercerization as pretreatment for the deep dyeing of ramie fibre

In order to produce deep shades of colour, ramie fibre was subjected to pretreatment by cationization, caustic mercerization (slack and tension condition), and liquid ammonia mercerization. The untreated and pretreated samples were dyed with 0.5 to 7 % concentrations (on mass of fiber (o.m.f)) of Liyuansol Red FL-2BL reactive dye. The dyeing properties of dye exhaustion, fixation, colour uniformity, wash fastness, and rubbing fastness were investigated. The results indicated that these pretreatments improved dye exhaustion and fixation on ramie fibre, with no loss of fastness. For the untreated and treated substance, the amount of dye mass absorption increased linearly with increased dye o.m.f. Cationic treatment improved performance, with 89 % and 98 % for exhaustion and fixation, respectively, and the maximum K/S values of all fibers receiving pretreatment. The colour uniformity was acceptable and similar for the untreated and treated ramie fibers, with the exception of cationic-treated fabric dyed at 7 % dye o.m.f that showed a high standard deviation value of colour uniformity. The Freundlich and Langmuir adsorption isotherm models were also used to study the adsorption of dye on ramie fibre; all of the adsorption processes fit the Freundlich model.     

Coating superfine down powder on polypropylene for the production of dyeable fibers

To develop dyeable isotactic polypropylene (iPP) fibers, superfine down powder (SDP) was coated on the surface of iPP fibers post melt-spinning. Optical micrographs showed that the surface of powder-coated iPP fibers was roughness, and the amount and dispersion of coated SDP were found entirely dependent on melt-spinning temperature. With the increase in coated SDP content, the moisture and water absorption of powder-coated iPP fibers increased. Powder-coated iPP fibers could be, respectively, dyed by reactive red dye and acid red dye, and the observed enhancement of color strength (K/S) and red value (a*) of powder-coated iPP fibers could be attributed to SDP coated on iPP fibers. It was worth noting that the removal of coated SDP affected the wet-washing fastness of powder-coated iPP fibers largely. In addition, the powder-coated iPP fibers were produced in a few minutes with lower cost and could have potential applications in textile industry.