Dye Mixture Research Articles

A green approach for dyeing cotton fabrics using synthesized reactive disperse dyes and their mixtures under supercritical CO2 medium.

Dyeing natural fabrics using supercritical carbon dioxide is challenging, especially without essential color hues. This work demonstrated that two newly developed reactive disperse dyes with distinct colors and shades were generated, one of which featured from the anthraquinone family and the other yellow, containing a pyrazole moiety. These new dyes and their combinations were used to dye cotton fabric using supercritical carbon dioxide and the highest K/S values were achieved at 8.73 for the mixture of (blue dye: yellow dye 80:20), however the lowest K/S was observed at 7.71 for (blue dye: yellow dye 20:80). The new dyes' chemical compositions were identified using elemental and spectroscopic analyses. The effectiveness of these dyes and their mixtures for cotton dyeing was discussed. The dyed samples were tested for color fastness, and the results indicated that they had excellent color retention and were highly durable in washing. The increasing patterns in both dyeing rate and build-up curves show good compatibility. Furthermore, desirable shades of green can be achieved by mixing blue and yellow dyes at various ratios in supercritical CO2. The compatibility test involves calculating color difference index values for dyed cotton fabrics by utilizing various ratios of a binary mixture of dyes. Furthermore, the dyes under study and dyed samples displayed superior antibacterial properties against gram-positive and gram-negative bacteria compared to certain antibiotics used as a control. These results aligned with the quality and eco-friendly standards required by the industry without the use of water.

Spectral and Linear Optical Properties for New Mixture of Nile Blue and Malachite Green Organic Laser Dyes

Spectral and Linear Optical Properties for New Mixture of Nile Blue and Malachite Green Organic Laser Dyes

Enhanced Efficiency of Dye-Sensitized Solar Cells Using Nitrogen-Titanium Dioxide Composites and Optimized Azo Dye Mixtures

In response to the increasing global energy demand, developing cost-effective and reliable renewable energy sources is crucial. Dye-Sensitized Solar Cells (DSSCs) have emerged as a promising alternative due to their low production cost, flexibility, and capability to operate under diffuse sunlight. This study aims to enhance the efficiency of DSSCs by incorporating Nitrogen-Titanium Dioxide (N-TiO2) composites synthesized via the Sol-Gel method [1]. The DSSCs were constructed using N-TiO2 composites in conjunction with VC, RP, and RM azo dyes. Nitrogen in the TiO2 matrix effectively reduced the band gap, leading to improved light absorption. The presence of Nitrogen dopants is expected to introduce additional energy levels within the TiO2 bandgap, enhancing light absorption and charge carrier separation, which are crucial factors for improved DSSC performance [2,3]. The current-voltage (I-V) characteristics of the DSSCs revealed significant variations in key performance metrics, including short circuit current (Isc), fill factor, and power conversion efficiency. Specifically, DSSCs utilizing N-TiO2 with VC-RP dye mixture achieved a higher efficiency of 0.349%, an Isc of 0.85 mA, and a fill factor of 44.59%, with Rs and Rsh values of 328.13Ω and 1637.18Ω, respectively [4]. These results underscore the potential of N-TiO2 composites, particularly when paired with optimized dye mixtures, to significantly enhance the electronic properties and overall efficiency of DSSCs.

Adsorption behavior of cationic dyes on starch nanocrystals: Kinetic, isotherm, and thermodynamic insights from single to multi-component systems

The adsorptive potential of starch nanocrystals (SNCs) was evaluated for the elimination of methylene blue (MB), crystal violet (CV), and malachite green (MG) from aqueous media in single, binary, and ternary dye systems using batch mode experiments. SNCs were extracted using mild acid hydrolysis to remove the amorphous parts of native granular starch, and they were characterized using different physicochemical methods, such as FESEM, XRD, FTIR, BET, TGA, and pHZPC. The results revealed that the optimal pH for dye removal in both single and mixed dye systems was found to be 9.0. The equilibrium time increased from 5 to 20 min when the system was changed from single to binary, and then further increased to 30 min when the system was changed to ternary. The equilibrium data for single-dye systems exhibited a good fit with the Langmuir isotherm model (R2 > 0.98, SEE <3.52 mg g−1), whereas for binary and ternary dye mixtures, the extended Langmuir model provided an accurate representation of the experimental data (R2 > 0.99, SEE <1.33 mg g−1). Among the single, binary, and ternary systems, the highest adsorption capacities were observed for MB, MB in the (MB + MG) binary system, and MB in the (MB + CV + MG) ternary system. The respective adsorption capacities were recorded as 79.55 mg g−1, 61.91 mg g−1, and 43.59 mg g−1. The adsorption of dyes onto the SNCs was inherently spontaneous and endothermic, and adhered to the pseudo-second-order kinetic model in single dye systems as well as mixed dye systems. It can be concluded that the SNCs are capable of being utilized for five consecutive cycles in the adsorption-desorption process for single dye systems and three consecutive cycles for mixed dye systems. This suggests that the SNCs have potential as a sustainable and efficient option for dye removal in mixture systems.

Optimizing the photocatalytic properties Er-doped bismuth ferrite for the degradation of mixed dyes under sunlight irradiation

In this study, the erbium (Er)-doped bismuth ferrite (BiFeO3/BFO) with the chemical formulation of Bi1-xErxFeO3 (x = 0, 5, 10, and 15 mol%) are synthesized using hydrothermal method. It is found that Er-doping induces structural distortions in BFO, leading to improved electronic and optical properties in BFO as confirmed by XRD, XPS, UV–visible absorption and PL spectral analysis. The particle size of BFO is found to be decreasing in the range of 60–30 nm with Er-doping, observed from their TEM images. Further, the photocatalytic efficiencies of the synthesized Bi1-xErxFeO3 nanoparticles are studied towards the degradation of methylene blue (MB), rhodamine B (RhB) dyes and their mixture under solar irradiation. While all the Er-BFO showed improved efficiency compare to pristine, the 10 mol% Er-doped BFO showed the highest degradation of ∼99 and 94 % for MB and RhB dyes, respectively in 180 min. More interestingly, while the pristine BFO selectively degraded only the MB dye in the MB-RhB mixture, the Er-BFO greatly degraded both the dyes in the mixture, which attributed to their improved electronic, electric field and optical band structure properties, especially to the 10 % Er-BFO degraded around 93 and 78 % of MB and RhB dye in the MB-RhB mixture. The cyclical use of 10 mol% Er-BFO is tested toward the degradation dye mixture, which showed a consistent photocatalytic performance up to 5 cycles, suggesting that the Er-doped BFO is photochemically stable and suitable for sustainable photocatalytic applications.

Tailored nano clay blends for enhanced dye mixture adsorption in wastewater treatment

Natural clays are eco-friendly, cost-effective, and industrially acceptable adsorbents employed in wastewater treatment. Textile effluents contains mixture of dyes where a single adsorbent often fails to treat completely. Herein, the simplest strategy for the efficient treatment of effluent with multicomponent pollutants using an tailored blend of two clay minerals has been presented. This strategy was studied using a binary blend of halloysite and montmorillonite clays (HAMT) to remove a mixture of industrial dyes, reactive Black-B (BB) and methyl red (MR) from the model effluent. Here, halloysite (HA) and montmorillonite (MT) selectively adorbs reactive black-B and methyl red respectively and could not completely treat model effluent individually whereas HAMT blend proved to be most effective. HAMT blend was prepared by convenient ultra-sonication assisted solution process and characterized using the various analytical techniques such as FT-IR, DR-UV spectra, XRD and SEM to determine structural, morphological features. Adsorption of model effluent studied as a function of pH, time, adsorbent loading and adsorbate concentration. The dye removal efficiency was remarkably enhanced when the HAMT blend was used according to the concentration of dyes present in the model effluent. The maximum dye removal efficiency was attained using HAMT (1:1) blend for effluent with an equimolar concentration of selected dyes. Similarly, HAMT (2:1) found suitable for the treatment of real textile effluent collected from local textile industries based on its assessment. This study aids in the development of a tailored adsorbent blend using conventional adsorbents for complex effluent treatment in a cost-effective way, eliminating the need for specialized materials.

Biosorption of Reactive Yellow 145 and Direct Blue 86 binary dye mixture by Ulocladium chartarum

Biosorption of Reactive Yellow 145 and Direct Blue 86 binary dye mixture by Ulocladium chartarum

Purification of textile wastewater by collective degradation using nanorods of cesium titanium bromide (CsTiBr3) perovskite

The present work recommends a sustainable environmentally safe method for the removal of textile dyes in an economically viable way.The wastewater expelled from the textile dying units contains a mixture of dyes. Here we address the challenge of using a single catalyst for the collective photocatalytic degradation of mixture of six dyes and two samples of textile effluents collected from a local dying unit under direct sunlight. The lead-free perovskite of CsTiBr3 nanorods prepared via the solvothermal process is effective in the collective photocatalytic degradation of dye mixture containing toxic dyes like congo red, crystal violet, malachite green, methylene blue, rhodamine, and methyl orange. The six-dye mixture turned colorless within three hours of direct sunlight exposure. The collective photocatalytic degradation ability of CsTiBr3 perovskite nanorods is successfully exploited for the degradation of the textile effluents. The chemical oxygen demand (COD) analysis guarantees the degradation of dye into non-toxic components. The recycling of wastewater is made possible by the removal of CsTiBr3 catalysts through adsorption using biochar derived from invasive plants. The biochars are extracted from invasive plants such as Acrostichum Aureum, Alternanthera bettzickiana, cyclosorus interrupts, and Quisqualis indica in which Acrostichum Aureum showed maximum adsorption. The scavenger studies using isopropyl alcohol (IPA), ethylene diamine tetra acetic acid (EDTA), and silver nitrate (AgNO3) suggest that holes control the photocatalysis mechanism.

Tuning the optical and photophysical characteristics of DR1 through mixing with JGB

A dye mixture of Disperse red1 (DR1) and Janus green B (JGB) was prepared with different concentrations of the two dyes. The optical properties were studied for the two dyes and their mixtures in terms of the absorbance spectra. The direct optical energy gap in addition to the refractive index, extinction coefficient, dielectric constant and optical conductivity were estimated to the two dyes and their mixtures. The experimental energy gap was found to be 2.234 and 1.666 eV for DR1 and JGB respectively, while the values of the energy gaps for the mixtures were found to be ranging between these two values. On the other hand, the refractive index was found to be changed in a systematic way by changing the contents of the dye mixture. The same behavior was also observed for the dielectric constant and optical conductivity. The emission of the two dyes and their mixtures was studied in terms of fluorescence spectra using excitation wavelength of 300 nm where a change in the fluorescence intensity was observed by changing the contents of the mixture. Finally, TD-DFT simulations were performed for the two dyes and their mixture to study the electron density, electrostatic potential, energy gap and optical absorption spectrum and found to be compatible with the experimental measurements.

Application of cloud point extraction coupled with derivative spectrophotometry to remove binary mixture of Cresol Red and Methyl Orange dyes from aqueous solutions: Box–behnken design optimization

Cloud point extraction (CPE) was employed to eliminate Cresol Red (CR) and Methyl Orange (MO), as anionic dyes in a binary mixture from aqueous solutions. To remove these dyes Triton X-100 and NaCl at pH 5.7 were utilized. In this vein, wavelengths of 365 nm and 520 nm were respectively selected for CR and MO using the derivative spectrophotometer and first-order derivatives. According to based on the first-order derivative spectrophotometry, the recoveries rised from 94.3 to 99.5 % for CR and from 94.6 to 99.1 % for MO. In the following, the response surface methodology was administered to investigate the effect of surfactant concentration, temperature, and time on the dyes' elimination process. The quadratic mathematical model was obtained from the Box-Behnken design (BBD) matrix and developed to estimate the impact of each variable and its relationship with the elimination parameters. Later, coefficients of determination (R2) ≥0.97 were obtained using model equations and comparison between predicted and empirical values. Analysis of variance estimated the models’ significance and anticipation while processing the study variables. Based on the results, the model of pseudo-first-order in kinetic modelling can best describe dyes adsorption among the studied models. The analyzed dyes adhere to the Langmuir model with correlation values of 0.86 for CR and 0.87 for MO. The monolayer capacity (Qmax) was determined as 0.77 mol/mol for CR and 26.41 mol/mol for MO.

Novel magnetic metal ferrite-mango starch composite for the removal of dyes in single and ternary dye mixtures from aqueous solutions: kinetic and thermodynamic studies

ABSTRACT Magnetic metal ferrites attached to biowastes are proven to be promising adsorbents for the removal of dyes from water. Magnetic composites with biopolymers are gaining interest in the field of treatment of wastewater because of their selective nature, recyclability, low cost and environmental compatibility. In this work, Zinc ferrite composite with starch, extracted from mango seed kernel (ZFNMS) was synthesised. Characterisation techniques, such as FTIR, XRD, FESEM, BET, TGA and pHzpc, were used for the structural analysis of ZFNMS. ZFNMS was used to remove Methylene blue, Crystal violet and Brilliant green dyes in single and multiple (ternary) dye systems. The kinetics of adsorption by ZFNMS revealed that pseudo-second-order of kinetics was most appropriate for this study. Maximum adsorption capacities using ZFNMS for CV, BG and MB dyes were 142.9, 101.2 and 105.8 mg/g, respectively. The values of adsorption energies using ZFNMS were 200.5, 494.3 and 183.6 KJ/mol for CV, BG and MB dyes, respectively. Thermodynamic data revealed the spontaneous nature of the adsorption of dyes by ZFNMS and it was found that chemical adsorption was taking place in the present study. Regeneration of the adsorbent was done for successive five cycles and showed significant results. Thus ZFNMS is an ideal adsorbent for cationic dyes removal from water.

Purification of a reactive dyes mixture solution by means of pre-hydrolysed coagulants in the standard tests and coagulating flow system

Reactive dyes, widely used in textiles, often leach into sewage due to incomplete bonding with fibers. Coagulation offers an effective solution, yet standard lab tests for coagulation efficiency lack realism and are significantly labour and time-consuming. To address this, a novel approach is proposed: optimizing coagulation through a prototype lab flow. This system automates solution flow, reagent dosing, coagulation, and sludge separation via sedimentation and filtration. Tests reveal effective coagulation of various reactive dyes with pre-polymerized Al coagulants, but limited efficacy with Fe(III) coagulant. The flow system demonstrates mostly better purification results than jar tests, achieving around 95% colour removal with Al coagulants. This study highlights the efficacy of coagulation and filtration in jar tests, offering a simplified yet efficient method for assessing coagulation performance.

Highly energy-efficient degradation of simulated dye wastewater by array type underwater bubble discharge plasma: Key factors identification and degradation pathways

The extensive use of dyes presents a significant safety concern for the reuse of water resources, highlighting the critical need for a rapid and efficient degradation method for dye mixtures in wastewater. This study introduces a degradation system based on an array type underwater bubble discharge plasma specifically designed to treat a dye mixture wastewater containing methylene blue (MB) and methyl violet 2B (MV2B). Analysis of the optical and electrical characteristics reveals that the device experiences minimal temperature increase, with the highest intensity of the band associated with N2 in the emission spectra, and discharges occurring predominantly during the rising and falling edges of a pulse cycle. Experimental results demonstrate that the most effective degradation efficiencies (MB = 94.83%, MV2B = 93.48%) are achieved at an initial dye concentration of 50 mg/L, a power supply frequency of 6 kHz, an air flow rate of 2.5 SLM and an initial electrical conductivity of 50 μS/cm. The degradation of dyes is primarily attributed to the demethylation process of O3(aq) and other species. Toxicity analysis indicates that the plasma degradation process significantly reduces the toxicity of the intermediate products of dyes. This study not only presents a novel approach for treating high concentration mixed dye wastewater, but also provides valuable insights for future research in this area.

Biodecolorization of Azo Dye by Bacteria Alcaligenes faecalis Sub Sp. Phenolicus Isolated from a Bark-Beetle Tunnel Developed in Peltophorum Pterocarpum Plant

This study assessed the decolorization of reactive red 120 (RR120) by Alcaligenes faecalis subsp. phenolicus strain isolated from the bark borer insect (Indarbela tetraonis) tunnel developed in Peltophorum pterocarpum. The optimal parameters for the dye of decolorization 0.1 mg/L of dye were pH 7, temperature 35°C, fructose (0.4% w/v) as the carbon supply (0.4% w/v), peptone (0.2% w/v) as the nitrogen source (0.4% w/v), 12 hours of static conditions, and 0.3 ml of inoculums. Cell suspension, sodium alginate (3%, w/v), and PVA (5%, w/v) immobilized cell beads (10 beads 0.5 mm in size) were used in the batch continuous reactor for complete bio-decolorization of RR120. The batch reactor was subjected to 5 cycles of batches for 3 days of constant use. Under optimal conditions, the batch mode achieved more than 99% dye decolorization and fabric color removal in less than 48 hours of contact. When the control and dye-decolorized media were analyzed using UV spectroscopy, the absorbance of the control medium was higher than that of the decolorized media. GC-MS and FTIR analysis revealed the basic compounds and functional groups of the parent RR120 dye. This strain decolored 76.51% of AB 113, 96.8% of orange II, 98.47% of congo red, 98.3% of RR120, 97.92% of phenol red individual dyes, and 94.72% of the dye mixture at 12 hours. A. faecalis subsp. Phenolicus strains produced positive results in the qualitative analytical test of exopolysaccharides (EPS) and plant growth-promoting rhizobacteria (PGPR) production. The RR120 was decolorized in the presence of heavy metal ions by A. faecalis sub-sp. Phenolicus bacteria.

Green synthesis of a multifunctional β-cyclodextrin modified polymer sorbent using agrarian wastes of Nelumbo nucifera for the efficient sequestration of toxic dyes from polluted water

This study explores an eco-friendly strategy for the effective removal of toxic dyes Malachite Green, Methylene Blue, and Basic Magenta Dye, from water bodies, utilizing a novel β-Cyclodextrin modified Nelumbo nucifera (β-CDNN) sorbent. The sorbent was characterized using different analytical techniques, to assess its dye sorption capability. The analysis of sorption isotherm data revealed that the Freundlich model most accurately represented the equilibrium data. Kinetic studies indicated that the sorption process followed a pseudo-second-order model. At pH 5–8, the sorbent achieved maximum removal efficiencies of 96.7 %, 94.2 %, and 96.3 % for Malachite Green (402.7 mg/g), Methylene Blue (385.6 mg/g), and Basic Magenta Dye (401.03 mg/g), respectively, at equilibrium time 60 mins for MAG & MEB and 80 mins for MAD. The maximum swelling capacity of β-CDNN was recorded at 180.4 % and selectivity assay was performed via a MAG-AO7 dye mixture. The sorbent reusability was recorded for six consecutive cycles without much loss in efficiency. Additionally, β-CDNN exhibited a removal efficiency of 91.3 % in real dye samples. The findings highlight the rapid dye adsorption capabilities of β-CDNN, establishing it as a versatile, cost-effective, and environmentally friendly solution for water remediation, while also underscoring the beneficial use of bio-waste materials.

Multi-color emission composites of white carbon dots and dyes through inner filter effect

A series of multi-color carbon dot composites were obtained by transforming white carbon dots (WCDs) into three primary colors using the dyes' inner filter effect (IFE). WCDs were combined with three distinct dyes (methyl red, bromocresol green, and methylene blue), and three fluorescence colors (red, yellow, and blue) were obtained. The colors of the emitting light excited by the same UV light were similar to the colors of the respective dyes, and have a large Stokes shift. The presence of the IFE between WCDs and dyes was proved through a variety of methods, the analysis of the relationship between the UV of dyes and fluorescence spectra of WCDs, the excitation-emission matrix, as well as the comparison PL decay profiles of WCDs before and after dye addition. The Stern-Volmer quenching constant KSV exhibited no temperature dependence during the IFE process with increasing concentrations of dyes. The UV spectra of the mixture of WCDs and dyes were simply the sum of two individual components, which implies that there is no chemical interaction between WCDs and dyes. Since methyl red and bromocresol green are acid-base indicators, the fluorescence color of the carbon dot composite also changed continuously during the dilute NaOH solution titration process. In furtherment, distributing the binary system of “WCDs + dye” within poly (vinyl alcohol) (PVA), three colors fluorescent composite films of “WCDs / Dye / PVA” were produced successfully.

Novel Type of Non‐Toxic, Degradable, Luminescent Ratiometric Thermometers Based on Dyes Embedded in Disulfide‐Bridged Periodic Mesoporous Organosilica Particles

AbstractDespite the excellent thermometric performance of many developed luminescent nanomaterials, their use has not gone beyond proof‐of‐concept in vivo experiments to date. An important issue that needs to be resolved before moving toward true biomedical applications of engineered nanothermometers is their potential toxicity and bioaccumulation in the human body considering the ultimate objective of clinical applications. Since most reported nanothermometers currently are not degradable materials and are mainly based on the incorporation of heavy metal ions, these aspects remain of genuine concern in the fields of nanomedicine, nanobiotechnology, nanotoxicology, and nanopharmacology. This work explores the possibility of designing visible, as well as near‐infrared, emitting luminescent ratiometric nanothermometers based on appropriate organic dye mixtures embedded in hollow disulfide‐bridged periodic mesoporous organosilica (PMO) particles. Such hybrid particles show excellent thermometric performance in the physiological temperature range (20–50 °C), favorable degradability in simulated physiological conditions, as well as no toxicity to healthy normal human dermal fibroblast (NHDF) cells in a wide concentration range. Considering the simplicity of the approach from the synthetic point of view, and the large available library of known fluorescent dyes emitting in various regions of the electromagnetic range, this motif renders a very promising approach to designing novel non‐toxic, decomposable, luminescent ratiometric thermometers.

Synthesis and Dye Adsorption Dynamics of Chitosan-Polyvinylpolypyrrolidone (PVPP) Composite.

One major environmental issue responsible for water pollution is the presence of dyes in the aquatic environment as a result of human activity, particularly the textile industry. Chitosan-Polyvinylpolypyrrolidone (PVPP) polymer composite beads were synthesized and explored for the adsorption of dyes (Bismarck brown (BB), orange G (OG), brilliant blue G (BBG), and indigo carmine (IC)) from dye solution. The CS-PVPP beads demonstrated high removal efficiency of BB (87%), OG (58%), BBG (42%), and IC (49%). The beads demonstrated a reasonable surface area of 2.203 m2/g and were negatively charged in the applicable operating pH ranges. TGA analysis showed that the polymer composite can withstand decomposition up to 400 °C, proving high stability in harsh conditions. FTIR analysis highlighted the presence of N-H amine, O-H alcohol, and S=O sulfo groups responsible for electrostatic interaction and hydrogen bonding with the dye molecules. A shift in the FTIR bands was observed on N-H and C-N stretching for the beads after dye adsorption, implying that adsorption was facilitated by hydrogen bonding and Van der Waals forces of attraction between the hydroxyl, amine, and carbonyl groups on the surface of the beads and the dye molecules. An increase in pH increased the adsorption capacity of the beads for BB while decreasing OG, BBG, and IC due to their cationic and anionic nature, respectively. While an increase in temperature did not affect the adsorption capacity of OG and BBG, it significantly improved the removal of BB and IC from the dye solution and the adsorption was thermodynamically favoured, as demonstrated by the negative Gibbs free energy at all temperatures. Adsorption of dye mixtures followed the characteristic adsorption nature of the individual dyes. The beads show great potential for applications in the treatment of dye wastewater.

Removal of Congo red and tartrazine binary mixture using Leucaena leucocephala seed’s extract as natural coagulant

Abstract The textile industry is one of the industries that produces wastewater with complex contents and has the potential to pollute the environment. Consequently, wastewater treatment is required to prevent this problem. The utilization of natural coagulants to treat dye wastewater has been carried out by various researchers. However, most of the research only uses a single dye as the wastewater model, despite the complex nature of the real wastewater. Therefore, in this study crude extract of Leucaena leucocephala seed was used to coagulate single and binary dye mixtures with Congo red and Tartrazine as the model substance. The coagulation was carried out by varying the initial pH (3−9), dose of coagulant (50−1150 mg eq BSA/L) and the initial dye concentration (50−100 mg/L). It was found that Leucaena crude extract has successfully removed 99.54% of the Congo red (pH 3; dose 650 mg eq BSA/L) and 53.2% (pH 3; dose 1150 mg eq BSA/L) of Tartrazine at 50 mg/L single dye wastewater. The removal of 50 mg/L binary mixture was 94.4 and 54.6% for Congo red and Tartrazine, respectively, at pH 3 and coagulant dose 1050 mg eq BSA/L.

Textile color formulation methods: A literature review

AbstractColor has become an essential element in our communication and our judgment on products. In textile, the formulation of any color is an essential process to ensure color continuity from the master standard to all subsequent production batches. Indeed, the objective is to normalize its reproduction all along the color reproduction procedure. In the literature, researches concerning textile color formulation are important, so this review focuses on these different techniques and methods of color matching for dye mixtures and precolored fiber blends. This step involves determining the dyes or fibers to use (alone or in mixtures) and their appropriate proportions to reproduce the wanted colors. The main techniques used for dye mixtures are based on colorimetric, spectrophotometric, and artificial intelligence techniques. While for precolored fiber mixtures the used techniques are dived into theoretical and experimental models. In addition to the review of these different techniques, a quantitative analysis was carried out.