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Based on clarifying the structural difference between jade fibre and general polyester fibre, this paper aims to study the dyeing properties and dyeing adsorption mechanism of jade fibre with disperse dye and cationic dye.

The chemical structure and microstructure of jade fibre were briefly explained comparing with ordinary polyester fibre. The dyeing rate curve and dyeing adsorption isotherm of disperse dyes and cationic dyes on jade fibre were, respectively, studied. The dyeing uptake, dyeing absorption mechanism, and the main dyeing process parameters were proposed.

Jade fibre can be dyed with cationic dye and disperse dye. The suitable exhaust dyeing process is 110°C and 40 minutes for disperse dye, 100°C and 60 minutes for cationic dye. The dyeing uptake on jade fibre with both disperse dyes or cationic dyes is much higher than that on general polyester fibre and acrylic fibre, and the dyeing adsorption mechanism belongs to the combination of Langmuir and Nernst adsorption for disperse dyes and Langmuir adsorption for cationic dyes. Comparing with ordinary polyester fibre, jade fibre has the advantage of low temperature dyeing and reduced effluent, as is significant to energy-saving and emission reduction.

Jade fibre is a new type of modified polyester fibre with the function of health protection and energy conservation. There are little technical data in the literature at present about the dyeing property of jade fibre.

This study aims to demonstrate that orange-derived and lemon-derived systems can be used in continuous processes as efficient adsorbents to the entrapment of some anionic and cationic dyes in the textile dyeing wastewater effluents.

Physically and chemically modified orange and lemon mesocarps are used as natural adsorbents for the cationic dyes Basic Blue 3, Basic Yellow 21, Basic Red 18 and Basic Green 4 and the anionic dyes Acid Blue 264, Acid Yellow 49 and Acid Red 337, all commonly used in the textile dyeing industry. Adsorption capacities of the orange-derived and lemon-derived adsorbents on the dyes are studied simulating a batch and continuous industrial processes.

Results demonstrate that treated orange mesocarp (orange-derived adsorbent) can adsorb up to 97% of cationic Basic Green 4 in 30 min, whereas the lemon mesocarp (lemon-derived adsorbent) can retain up to 88% within the same time. In the case of anionic, 91% Acid Blue 264 is adsorbed by the orange mesocarp in 15 min, whereas 92% is adsorbed by the lemon homologue within the same time.

As far as the authors know, physically and chemically modified orange and lemon mesocarps have not been used on the removal of cationic (Basic Blue 3, Basic Yellow 21, Basic Red 18 and Basic Green 4) and anioinic (Acid Blue 264, Acid Yellow 49 and Acid Red 337) dyes of textile dyeing wastewater industry. It is a costless and efficient treatment that supposes, on the one hand, an eco-friendly and feasible process for discolouration of wastewater and, on the other, a valorisation (upcycling) of orange and lemon peels, which are not currently used.

The purpose of this paper was to study the dyeing properties of polysulphonamide (PSA)/aramid 1313 (MPIA) blended yarn by selecting suitable dyes and carriers required in the dyeing process.

Dyeing the blended yarn with cationic dyes, acid dyes, disperse dyes, reactive dyes and pigment, and comparing the shades, K/S values and fastness of the blended yarns.

The PSA/MPIA blended fibre is suitable for dyeing with the cationic dye at high temperature and pressure in the presence of carrier acetophenone, and good homochromatism is seen on the two fibres when using same type of dye.

PSA fibre is a thermo-resistant and flame-retardant product made in China in recent years. Blended with aramid 1313 fibre, it may acquire good spinnability. But there is little technical report about properties of the blended yarn in the literature at present. This paper reports the dyeing property of such fibres for the first time.

This study aims to evaluate the dyeing of the p-aramid fibre with cationic dyes and investigate the effect of dyeing in the protection of the fibre from ultraviolet (UV) light.

P-aramid fabric has been dyed with cationic dyes using benzyl alcohol as swelling agent to promote the penetration of dye molecules into the fibre. The fabrics were evaluated against colour strength (K/S) value and colour fastness properties after dyed with cationic dyes using full factorial design. This design was used to study the effect of factors that affect the response variables as well as to study the interactions among the factors on response variable. The bursting strength, scanning electron microscopy analysis and X-ray diffraction analysis of undyed and dyed p-aramid fabric were performed before and after exposure to UV light to investigate the changes in mechanical behaviour.

The results show that the p-aramid fabric dyed with cationic dyes has good K/S values and good fastness properties. The exposure of undyed p-aramid fabric to UV light causes serious loss in strength over short duration i.e. 40 h. Dyeing of p-aramid fabric enhances the resistance to UV light which reduces the loss in strength.

Most of the work is patented and no one has done the process optimization for the industry, so this study offers promising outcomes concerning the dyeing of p-aramid fabric with enhanced shade depth and good colour fastness characteristics.

The purpose of this study is to undertake surface graft copolymerization of viscose fabric via altering its fibrous properties by using acrylic acid (AA) as a carboxyl-containing monomer and peroxydisulfate (PDS) in presence of ferrous sulfate as a novel redox pair for initiating grafting. The latter process acted as an energy-saving process with respect to the reduction in polymerization temperature and maximizing the graft yield %, in addition to rendering the grafted viscose fabrics dye-able with cationic dye (crystal violet), which has frequently no direct affinity to fix on fabric.

To make graft copolymerization more efficient and economic, the optimum conditions for graft copolymerization were established. The graft yield % was determined as a function of initiator, catalyst and monomer concentrations and the material to liquor ratio, in addition to polymerization time and temperatures. Metrological characterizations via Fourier transform infrared spectroscopy and scanning electron microscopy of topographic morphological surface change have also been established in comparison with the ungrafted samples.

The maximum graft yield of 70.6% is obtained at the following optimum conditions: monomer (150 % based on the weight of fabric), PDS (50 m mole), ferrous sulfate (80 m mole) and sulfuric acid (30 m mole) at 40° C for 1.5 h using a liquor ratio of 30. Remarkably, grafting with AA enabled a multifold upsurge in color strength, with improvements in the fastness properties of cationically dyed grafted viscose fabric measured on the blue scale in comparison with untreated viscose fabric.

The novelty addressed here is undertaken with studying the effect of altering the extent of grafting of poly (AA)-viscose graft copolymers expressed as graft yield % in addition to carboxyl contents on cationic dyeing of viscose fabric for the first time in the literature. Moreover, rendering the viscose fabrics after grafting is dye-able with cationic dye with high brilliance of shades, which has regularly no direct affinity to fix on this type of fabrics.

Sulphur dyes are the most highly consumed colourants for cellulosic substrates owing to their reasonable cost and acceptable fastness. However, the use of noxious conventional reducing agent, sodium sulphide and impaired wash fastness against oxidative bleaching is gradually decreasing the market of these dyes. As the need for “Green” goods and services is raising public awareness, this paper aims to use a glucose-based biodegradable reducing agent in place of sodium sulphide to dye cotton fabrics with a range of commercial sulphur dyes. The study also proposes an aftertreatment method to improve the fastness properties of the dyeing.

The paper investigated the impact of a newly developed aftertreatment method on the fastness properties of dyeing. This involved the sequential application of a cationic fixing agent (Tinofix ECO) and tannin (Bayprotect CL) on the coloured fabrics and subsequent evaluation of colour strength, washing, light and rubbing fastness.

The effect of aftertreating the dyed cotton was found to significantly improve the light and wet rub fastness. The surface morphology of the dyeing remained unaffected as depicted by the absence of any finish residues.

The protective effect of the cation–tannin aftertreatments was examined with a view to providing the necessary commercial performance; however, it was established that the dry rub fastness was either reduced or remained unaffected and the wash fastness to International Organization for Standardization 105 C09 was also marginal.

This finishing technique is novel and can be found useful for manufacturing sulphur-dyed products with the improved light and wet rub fastness.

Nylon 6 fabric is pretreated with tannic acid and subsequently dyed with a cationic dye, Rhodamine B, from an aqueous dye solution and emulsion phase. The emulsion phase of n-hexadecane is emulsified by isopropyl alcohol and stabilized by Rhodamine B/tannic acid complex. Different factors affecting pretreatment and dyeing process have been studied. Changes of moisture regain, tensile strength, elongation and binding stiffness of the pretreated fabric are investigated.

The FTIR spectra of tannic acid pretreatment of nylon are also examined. The pretreated fabric with 10% owf tannic acid shows a slight increase in the tensile strength and elongation percentage. A higher moisture regain and binding stiffness are observed with increases in the amount of tannic acid. The results also indicate that the pretreatment for cationic dyed nylon 6 fabrics with tannic acid promote a higher dye uptake and cationic dye-based emulsion system with better fastness properties relative to those of the dye solution based system. A further improvement in wet fastness is secured by an aftertreatment of all dyed fabrics with a commercial anionic fluorescent whitening agent, Uvitex^® RSB 150%.

This study’s aim is to introduce a high-performance sorbent for the removal of both anionic (Congo red; CR) and cationic (methylene blue; MB) dyes from aqueous solutions.

Sodium silicate is adopted as a substrate for GO and AgNPs with positive charge are used as modifiers. The synthesized nanocomposite is characterized by FTIR, FESEM, EDS, BET and XRD techniques. Then, some of the most effective parameters on the removal of CR and MB dyes such as solution pH, sorbent dose, adsorption equilibrium time, primary dye concentration and salt effect are optimized using the spectrophotometry technique.

The authors successfully achieved notable maximum adsorption capacities (Qmax) of CR and MB, which were 41.15 and 37.04 mg g⁻¹, respectively. The required equilibrium times for maximum efficiency of the developed sorbent were 10 and 15 min for CR and MB dyes, respectively. Adsorption equilibrium data present a good correlation with Langmuir isotherm, with a correlation coefficient of R2 = 0.9924 for CR and R2 = 0.9904 for MB, and kinetic studies prove that the dye adsorption process follows pseudo second-order models (CR R2 = 0.9986 and MB R2 = 0.9967).

The results showed that the proposed mechanism for the function of the developed sorbent in dye adsorption was based on physical and multilayer adsorption for both dyes onto the active sites of non-homogeneous sorbent.

The as-prepared nano-adsorbent has a high ability to remove both cationic and anionic dyes; moreover, to the high efficiency of the adsorbent, it has been tried to make its synthesis steps as simple as possible using inexpensive and available materials.

In this study, polyvinyl alcohol (PVA)/poly[acrylic acid (AAc)-co-acrylamide (AM)] composite hydrogel was prepared by radical copolymerization in the presence of Fe³⁺ freezing-thawing method. The swelling behavior of the hydrogel was investigated. The novel synthesized hydrogel was used as an adsorbent for the removal of dyes from aqueous solutions. In this paper, methylene blue and maxilon blue 5G were selected as representative cationic dyes. In addition, adsorption isotherm models were used to describe the dye adsorption process.

The prepared composite hydrogel was characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, field emission scanning electron microscopy and UV–visible.

The prepared hydrogel exhibited excellent adsorption ability for both dyes. Various experimental conditions affecting the dye adsorption were explored to achieve maximum removal of both dyes. In addition, adsorption isotherm models were used to describe the dye adsorption process.

To the best of the author’s knowledge, synthesis of PVA/poly(AAc-co-AM) composite hydrogel in the presence of Fe³⁺ and investigation of the removal of methylene blue and maxilon blue 5G dyes is done for the first time successfully.