Comparative Study on the Microwave-Assisted and Conventional Dyeing of Polyamide Fabric with Acid Dyes

1. Introduction

Nylon is the one of the most important synthetic fibers in textile industry which is usually dyed with acid and metal complex dye. Nylon is well known for its durability, lightweightness, greater tensile strength, and damage resistance propoerties. Nylon has the advantages over cotton fiber in achieving high color strength. Polyamide fibers, particularly nylon 6 and nylon 6.6, represent a cornerstone of the contemporary textile industry. Their widespread application, ranging from high-performance apparel to advanced technical textiles, stems from their exceptional physiomechanical properties, including superior tensile strength, elasticity, and remarkable abrasion resistance. The coloration of these versatile materials is predominantly achieved through the use of acid dyes, which form robust ionic interactions with the protonated amino groups inherent in the polyamide fiber structure. This interaction ensures excellent dye affinity, colorfastness, and the production of vibrant, durable shades.[1,2,3,4,5,6,7,8,9,10,11]

Acid dyes represent the most commonly used class of dyes for polyamide fiber dyeing due to their excellent affinity and color fastness properties. The dyeing mechanism involves ionic interactions between the sulfonic acid groups of the dye molecules and the amino groups present in the polyamide fiber structure. The dyeing process is typically conducted under acidic conditions (pH 4-6) to protonate the amino groups in the fiber, thereby enhancing the electrostatic attraction between the dye and fiber [12,13,14,15,16].

Microwave treatment is one environmental friendly less time consuming conditions and the more energy saving phenomenon. Microwave radiation is presented as a substituted for conventional heating methods since it offers even, rapid and efficient heating by aiding all particles to heat up simultaneously. In response to the growing demand for sustainable and efficient manufacturing paradigms, microwave-assisted dyeing has emerged as a revolutionary alternative technology. Microwave tratment improves the fabric’s uptake ability and coloring characteristics. Microwave irradiation is part of th recent most simple, lower cost and valued technologies in textile dyeing [16,17]. The fundamental principle underpinning microwave heating is dielectric heating, whereby electromagnetic radiation, commonly at a frequency of 2.45 GHz, induces rapid molecular vibration and rotation of polar molecules, predominantly water, within the dyebath. This unique mechanism results in rapid, uniform, and volumetric heating throughout the entire dyeing system, a stark contrast to the slower, less uniform, and surface-to-core heat transfer characteristic of conventional heating methods. This internal generation of heat promises to dramatically curtail processing times, reduce energy consumption, and increase dye diffusion and fixation within the textile substrate.[18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45].

Recent scholarly investigations have increasingly underscored the transformative potential of microwave technology across diverse textile applications [18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45].

This study is designed to conduct a detailed comparative analysis of both conventional and microwave-assisted dyeing techniques for polyamide 6 fabric utilizing a model acid dye (Telon Blue M-2R). The research will systematically investigate the effects of key process parameters specifically temperature, dye concentration, dyeing time, and pH on the dyeing mechanism, ultimate dye uptake, and final color strength. The overarching goal is to furnish a robust scientific foundation that will facilitate the development of more efficient, economically viable dyeing protocols for polyamide textiles [44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65].

2. Materials and Methods

2.1. Materials

The substrate used for all dyeing experiments was a 100% polyamide 6 (PA6) fabric. The fabric was procured from Nurel Group (Turkey). Fabric contains different type polyamide yarn. %35 384T-70/24 Denier Polymaide FDY Semidull, %10 192T-40/13 Denier Poliamide FDY Semidull, %55 - 300 DN-70/24*4 Denier Texture Polyamide Semidull.

Polyamide 6 (PA6) is synthesized via the ring-opening polymerization of e-caprolactam. The resulting polymer chain contains repeating amide groups (CONH), which constitute the majority of the polar sites. The polymer chains are terminated by a small number of carboxylic end groups (COOH) and amino end groups (NH). Since the number of strongly hydrophilic end groups is low relative to the less-hydrophilic amide groups, the fiber exhibits low swelling in aqueous media, which in turn makes dye penetration difficult [1,2,3,4,5,6,7,8,9,10,11].

The preliminary preparation of the fabrics was conducted at Nurel Tekstil. The greige fabrics were initially processed through a Binaco Happy Scour continuous washing machine using Bianco HS New detergent at 85 °C and a speed of 30 m/min. Subsequently, the fabrics were passed through a stenter at 195 °C and 30 m/min. to ensure dimensional stability. Chemical agents were employed in the dyebath to achieve a more uniform dyeing process. Specifically, a biodegradable detergent, Bianco HS New, which is compatible with the dyebath and effectively removes impurities from the fabric, was utilized in conjunction with a levelling agent.

Our dyed lace fabric contains four different polyamide yarns. It is more important for us to observe that all fibers are dyed uniformly and closely together, rather than focusing solely on the dye uptake of a single fiber. Our spectrophotometric readings, from which we obtained the K/S (Kind/S) values, were taken from three different points, and the average values were used. It was observed that the deviations were not significant.

Conventional dyeing experiments were conducted in a laboratory-scale, using Rapid Eco-Dyer Laboratory Machine.

The acid dye selected for this investigation was C.I. Acid Blue 324, commercially known as Telon Blue M-2R, supplied by DyStar (Germany). This dye possesses a molecular weight of 766.53 g/mol and was used as received with a purification. The chemical structure of the dye is depicted in Figure 1 [12,13,14,15,16].

For pH control and adjustment of the dyebaths, analytical grade acetic acid (glacial, 99.8%) was used to prepare appropriate buffer solutions.

2.2. Dyeing Procedures

2.2.1. Conventional Dyeing Methodology

Conventional dyeing experiments were conducted in a laboratory-scale. The dyebath was prepared with a liquor ratio of 1:50. The dyeing process was initiated at a starting temperature of 30 °C. The temperature was then uniformly raised to the target dyeing temperature (50, 60, 70, 80, or 95 °C) at a controlled rate of 1 ⁰C/min. The dyeing was maintained at the final temperature for a duration of target reaction time (5-10-15-20-25-30 minutes) for comparative studies. Upon completion of the dyeing duration, the fabric samples were immediately removed, thoroughly rinsed with cold deionized water to remove any unfixed surface dye, and subsequently air-dried [44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65].

In addition, the effects of other reaction parameters such as pH (3, 3.5, 4, 4.5, 5, 6) and dye concentrations (0.1%, 0.25%, 0.5%, 0.75%, 1%, 1.5%) on dyeing were investigated at a different reaction times and conditions which are detailed in related sections [44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65].

2.2.2. Microwave-Assisted Dyeing Methodology

Dyeing experiments were conducted using a modified microwave oven (Milestone Start D Microwave Digestion System). Dyeing baths were prepared in microwave-transparent 100 ml capacity tubes to ensure uniform microwave energy absorption.

The dyebath was prepared using the same liquor ratio (1:50) and dye concentrations as in the conventional dyeing protocol [44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65]. The microwave power was systematically varied and set to 160 W. The dyeing duration was varied from 30 to 270 seconds (0,5 – 4,5 minutes), depending on the specific experimental conditions. Post-dyeing, the fabric samples were treated in the same manner as the conventionally dyed samples, involving a thorough rinsing and air-drying process [16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45].

Additional experiments were conducted to observe the effects of reaction time and reaction temperature at a different conditions which are detailed in related sections [16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45].

2.3. Analytical Procedures

2.3.2. Colorimetric Measurement

Dye uptake was determined by measuring the color strength in the fabric at predetermined time intervals using a Data Color SF 600 spectrophotometer at the maximum absorption wavelength of Telon Blue M2R (λ_max = 630 nm). A calibration curve was established using known concentrations of the dye.

Color strength (K/S value) of the dyed fabric samples was measured using a reflectance spectrophotometer (Data Color 1000 spectrophotometer.) according to the Kubelka-Munk equation:

$${\displaystyle \frac{K}{S}}={\displaystyle \frac{\left(1-R\right)²}{2R}}$$

(1)

where R is the reflectance value at the maximum absorption wavelength [44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65].

The percentage dye exhaustion (Dye Exhaustion is proportional with K/S) was calculated using the following equations:

$$\mathrm{\%}\mathrm{E}\mathrm{x}\mathrm{h}\mathrm{a}\mathrm{u}\mathrm{s}\mathrm{t}\mathrm{i}\mathrm{o}\mathrm{n}={\displaystyle \frac{\left({\mathrm{C}}_0-\mathrm{C}\mathrm{ₜ}\right)}{{\mathrm{C}}_0}}\mathrm{x}100$$

(2)

$$\mathrm{K}/\mathrm{S}\propto {\displaystyle \frac{\left({\mathrm{C}}_0-\mathrm{C}\mathrm{ₜ}\right)}{{\mathrm{C}}_0}}\mathrm{x}100$$

(3)

$${\displaystyle \frac{\mathrm{K}}{\mathrm{S}}}={\displaystyle \frac{\left({\mathrm{C}}_0-\mathrm{C}\mathrm{ₜ}\right)}{{\mathrm{C}}_0}}\mathrm{x}\mathrm{A}$$

(4)

where C₀ is the initial dye concentration and Cₜ is the dye concentration in the bath at time t [44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65].

The time-dependent calculation of dye concentration (C_t) in water was determined by using spectrophotometric measurements of the dye-water mixture and the proportionality of the K/S value to dye consumption.The difference between the initial concentration and the dye concentration remaining in the bath at time (t) gives the dye concentration absorbed by the fabric [44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65]. Additionally, a linear regression was performed between this value and the K/S value read by the spectrophotometer to confirm the relationship of K/S value with the concentration. This conversion coefficient (A) was determined to be approximately 15. This coefficient depends on the type of dye and the initial dye concentration.

3. Results and Discussions

3.1. Conventional Dyeing

3.1.1. Effect of PH

Figure 2 and Table 1 show the relationship between the initial pH of the dye bath and the resulting color strength (K/S) of the dyed material. The experiment was conducted under constant conditions of time (20 minutes) and temperature (80 °C), with a dye concentration of 1% in conventional media. The results, presented in Figure 2 and Table 1 clearly demonstrate a strong inverse correlation between the initial dye bath pH and the resulting K/S value.

The data in Figure 2 and Table 1 show that the highest color strength was achieved at the lowest initial pH of 3.0, while the lowest color strength was recorded at the highest initial pH of 6.0. This represents a significant decrease of approximately 47.5% in color strength as the initial pH is increased from 3.0 to 6.0.

The plot of K/S versus pH exhibits a distinct negative exponential relationship. As the pH increases, the K/S value decreases sharply, particularly in the highly acidic range pH 3.0 to 4.0, before the rate of decrease moderates at higher pH values (above 4.5).

The data shows a progressive decrease in K/S as pH increases, with the steepest decline occurring between pH 3.0 and 4.0 (13.9% decrease per 0.5 pH unit). This indicates that the pH range 3.0–4.0 is critical for maximizing dye fixation on polyamide fibers. Poliamide fibers can be easily degraded if exposed to lower pH for a long time. At the same time, the exhaustion of dye molecules only triggers when kept at acidic pH [10].

3.1.2. Effect of Time andTemperature

The K/S value is a measure that indicates the color depth or dye uptake of a material The Kubelka-Munk function is widely used in color science to quantify the color yield of a dye on a substrate, where a higher K/S value indicates greater color depth or strength. [44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65].

The analysis were conducted to understand the effects of the different dyeing times and the different temperatures at a pH 6-7 (without acid donor) and a dye concentration of 1%. The dye samples at 1% concentration were heated to target temperatures (50 °C, 60 °C, 70 °C, 80 °C, and 95 °C). Figure 3 and Figure 4 show the change in K/S values and dye concentration over time (minutes) for five different temperatures. K/S values at 0, 5, 10, 15, 20, 25, and 30 minutes were measured for each temperature. Generally, K/S values show an increase over time at all temperatures. As the temperature increases, both the final level of K/S values and the rate of reaching saturation increase. Analysis of conventional dyeing curves and dyeing data in Figure 3 and Figure 4 and Table 2 and Table 3 clearly demonstrates that temperature and time play critical roles in K/S values and dyeing mechanism. At the highest temperature of 95 °C, the fastest dye uptake and the highest final K/S values were obtained.

The rate of dye exhaustion is profoundly influenced by temperature. As the temperature increases from 50 °C to 95 °C, the initial rate of dye uptake increases significantly. More importantly, the time required to reach equilibrium is drastically reduced. For instance, the 95 °C curve shows a near-complete exhaustion (minimal change in concentration) within the first 10–15 minutes, whereas the 50 °C curve continues to show a measurable, albeit slow, decrease in concentration even after 30 minutes (Figure 4 and Table 3).

3.1.3. Effect of Dye Concentration According to Different Temperatures

The dyeing process was initiated at a starting temperature of 30 °C to examine the effects of dye concentration on the reaction. The temperature was then uniformly raised to the target dyeing temperature (50, 60, 70, 80, 90 or 95 °C) at a controlled rate of 1 °C/min. Experiments were proceeded in the pH 6-7 (without acid donor) and a reaction time of 10 minutes to investigate the effects of different dye concentrations and temperature. Figure 5 and Figure 6 and Table 4 illustrates the relationship between color strength, dye concentration, and dyeing temperature for a conventional dyeing process.

For any given dye concentration from Figure 5 and Table 4, an increase in temperature from 50 °C to 95 °C results in a substantial increase in the K/S value. These data shows that the dyeing process has a critical temperature zone where the mechanism of dyeing are dramatically accelerated.

The K/S value under these conditions is approximately 3.5 times greater than the value achieved at the same concentration but at 50 °C. This underscores the synergistic effect where a high dye concentration and high thermal energy (temperature) work in concert to maximize dye adsorption and fixation.

The Conventional Dyeing Curve presented in Figure 6 illustrates the relationship between temperature and color strength (expressed as K/S values) for varying dye concentrations ranging from 0.1% to 1,5%.

At all temperatures, higher dye concentrations result in higher K/S values, confirming that color strength is concentration-dependent. However, the relationship is non-linear, especially at elevated temperatures:

• At lower concentrations (0.1%), K/S values remain relatively low even at high temperatures, indicating limited availability of dye molecules.
• At higher concentrations (0.75% and 1,5%), K/S increases sharply up to 80–90 °C, after which the rate of increase diminishes. This behavior suggests site saturation within the fiber, where additional dye molecules contribute less effectively to color strength.

Notably, the 1,5% dye concentration exhibits the highest K/S values across all temperatures, reaching a maximum of approximately 15,91 at 95 °C, confirming superior dye loading under these conditions.

As observed, K/S values increase with rising temperature across all dye concentrations, indicating enhanced dye uptake and fixation at elevated temperatures.

For all dye concentrations, an overall increase in K/S is observed as the temperature increases from 50 to 95 °C. This trend can be attributed to several temperature-dependent phenomena:

Increased molecular mobility of dye molecules, which enhances diffusion from the dye bath into the fiber structure. Fiber swelling at elevated temperatures, leading to greater accessibility of internal dye-binding sites. The most pronounced increase in K/S occurs between 70 and 90 °C, particularly for dye concentrations of 0.5%, 0.75%, 1% , % 1.5, suggesting that this temperature range represents a critical transition where dye diffusion becomes significantly more efficient. Beyond 90 °C, the increase in K/S becomes marginal, indicating an approach to dye saturation or equilibrium uptake.

3.2. Microwave Dyeing

3.2.1. Effect of PH

Table 5 and Figure 7 shows the relationship between the initial pH of the dye bath and the resulting color strength (K/S) of the dyed material in microwave media. The experiment was conducted under constant conditions of time (4 minutes) and temperature (80 °C), with a dye concentration of 1% in microwave media. The primary objective is to identify the optimal pH range for maximizing color yield in microwave media.

The results from Figure 7 and Table 5 demonstrate a strong inverse correlation between the initial pH of the dye bath and the color strength. The highest K/S value was achieved at the most acidic condition tested pH 3.0 as in conventional media.

The K/S value decreases sharply from a maximum of approximately 25.0 at pH 3.0 to 12.5 at pH 6.5. This reduction of nearly 50% in color strength highlights the paramount importance of pH control in the dyeing of polyamide fibers, particularly when using acid or metal-complex dyes [12,13,14,15,16].

The high K/S values achieved (up to 25.0) are indicative of a highly efficient dyeing process, which is likely enhanced by the microwave environment.

• Accelerated Diffusion: Microwave heating provides rapid, volumetric heating, which can significantly increase the molecular mobility of the dye and the segmental motion of the polymer chains. This effectively lowers the energy barrier for the internal diffusion of the dye into the fiber matrix, accelerating the overall dyeing rate and allowing for a higher equilibrium dye uptake in a shorter time [16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45].
• Synergistic Effect: The microwave energy acts synergistically with the optimal chemical conditions (pH: 3- 6). While the acidic condition provides the necessary thermodynamic driving force (electrostatic attraction), the microwave energy provides acceleration (enhanced diffusion), resulting in the superior color strength observed[16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45].

Both conventional and microwave-assisted dyeing show a clear, inverse relationship between pH and color strength. The K/S value is maximized at the lowest tested pH (pH 3.0) and decreases sharply as the dyebath becomes less acidic. The optimal pH for maximum dye uptake remains consistently at pH 3.0 for both conventional and microwave-assisted dyeing [10].

3.2.2. Effect of Time and Temperature

The analysis were conducted to understand the effects of the different dyeing times and the different temperatures at a pH 6-7 (without acid donor) and a dye concentration of 1%.

Figure 8 and Figure 9 and Table 6 and Table 7 show the effect of temperature (50– 95 °C) on the measured parameter over a 10 minute heating period. At all tested temperatures, the parameter increased continuously with time, indicating a temperature-dependent process. However, the rate of increase varied considerably with temperature.

Microwave-assisted dyeing is an advanced technique that utilizes electromagnetic radiation to rapidly heat the dye bath and the substrate, leading to faster diffusion and reduced processing times compared to conventional methods. The color strength, quantified by the Kubelka-Munk function (K/S), is a critical parameter for evaluating the efficiency of the dyeing process.

Temperature Dependence: For any given time point, the K/S value is directly proportional to the temperature. The 95 °C curve consistently yields the highest color strength, while the 50 °C curve yields the lowest.

The initial rate of dyeing (the slope of the curve at t=0) is significantly higher at elevated temperatures, particularly at 80 °C and 95 °C. The 95 °C curve exhibits a near-vertical rise in the first minute, achieving a K/S of 11.530, which is approximately 8.2 times the value achieved at 50 °C (K/S = 1.399) in the same period.

Equilibrium/Saturation: All curves exhibit a characteristic trend of rapid initial uptake followed by a gradual leveling off, suggesting that the dyeing process is approaching equilibrium exhaustion. The saturation point is reached fastest and at the highest K/S value for the 95 °C process.

Dye exhaustion, the percentage of dye transferred from the bath to the textile substrate, is a critical parameter in industrial dyeing, directly impacting color yield, process economics, and environmental sustainability. Monitoring the dye concentration in the bath over time is the standard method for determining the exhaustion rate. This analysis interprets the provided concentration data to quantify the effect of temperature on the rate and extent of dye uptake in a microwave-assisted system [44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65].

The data in Figure 9 and Table 7 clearly demonstrate the exponential relationship between temperature and dye exhaustion. The analysis of the dye bath concentration data confirms the superior efficiency of high-temperature microwave-assisted dyeing. The process at 95 °C achieves an exceptionally high dye exhaustion of 95.2% in just 10 minutes, which is indicative of a highly accelerated mass transfer process. This rapid and near-complete exhaustion is a direct result of the thermal energy provided by the microwave, which enhances the diffusion coefficient of the dye molecules and the swelling of the fiber structure. These findings underscore the potential of microwave technology for developing fast, high-yield, and environmentally conscious dyeing protocols.

The comparative analysis unequivocally demonstrates that microwave-assisted dyeing is superior to the conventional method. The microwave process significantly accelerates the rate of dye uptake, leading to substantially higher dye exhaustion in a fraction of the time required by the conventional method. This efficiency is particularly pronounced at 95 °C, where the microwave method achieves near-complete exhaustion 95.2% in just 10 minutes. The enhanced performance is attributed to the rapid, volumetric heating characteristic of microwave energy, which facilitates faster dye diffusion and fixation. These findings support the adoption of microwave technology as a more time-efficient and environmentally favorable alternative for industrial dyeing applications.

3.2.3. Effect of Dye Concentration According to Different Times

The analysis were conducted to understand the effects of the different dyeing times and the different concentrations at a pH 6-7 (without acid donor) and average temperature of 80 °C.

Table 8 and Figure 10 and Figure 11 illustrate the relationship between dye concentration (% mg/100 ml) and color strength (K/S) for samples treated under microwave irradiation at different dyeing times (0–4.5 minutes).

Overall, the results demonstrate that both dye concentration and microwave dyeing time have a significant positive effect on color strength. For all microwave exposure times, the K/S values increase with increasing dye concentration. This trend indicates that higher dye availability in the dye bath leads to greater dye uptake by the material, resulting in enhanced color strength. However, the increase is non-linear, suggesting a gradual approach toward saturation at higher concentrations.

At a fixed dye concentration, increasing the microwave treatment time markedly increases the K/S values. Short dyeing times (0–1.5 minutes) result in relatively low color strength, while longer times (3–4.5 minutes) produce substantially higher K/S values. This behavior can be attributed to the enhanced molecular mobility and diffusion of dye molecules under microwave heating, which promotes more efficient dye–fiber interactions.

The highest color strength is observed at the combined condition of high dye concentration and prolonged microwave exposure (4–4.5 minutes). This indicates a synergistic effect, where microwave energy accelerates dye penetration and fixation, particularly at higher dye concentrations.

The data suggest that microwave-assisted dyeing is an effective method for achieving high color strength in relatively short processing times. Optimizing microwave exposure time can reduce energy consumption while maintaining or enhancing dyeing efficiency.

The results in Figure 10 and Figure 11 and Table 8 clearly demonstrate that both dye concentration and microwave exposure time have a pronounced effect on dye uptake. For all dye concentrations studied (0.1–1.5%), the K/S values increase monotonically with dyeing time, indicating progressive adsorption and fixation of dye molecules onto the substrate. A rapid increase in K/S is observed at the early stages (0–2.5 min), followed by a more gradual rise at longer times.

At any given dyeing time, K/S values increase systematically with increasing dye concentration:

${\mathrm{K}/\mathrm{S}}_{1.5\mathrm{\%}}>{\mathrm{K}/\mathrm{S}}_{1.00\mathrm{\%}}>{\mathrm{K}/\mathrm{S}}_{0.75\mathrm{\%}}>{\mathrm{K}/\mathrm{S}}_{0.5\mathrm{\%}}>{\mathrm{K}/\mathrm{S}}_{0.25\mathrm{\%}}>{\mathrm{K}/\mathrm{S}}_{0.1\mathrm{\%}}$

This trend confirms that higher initial dye concentrations provide a greater driving force for mass transfer, leading to enhanced dye uptake. The effect is particularly pronounced under microwave conditions, where volumetric heating promotes:

• Faster dye diffusion
• Improved fiber swelling
• Increased accessibility of internal binding sites

At higher concentrations (≥0.75%), the K/S values increase sharply after 3 minutes, suggesting that microwave irradiation effectively overcomes diffusion limitations that are typically observed in conventional dyeing processes.

3.3. Fastness Properties

Color fastness tests were performed according to ISO standards for fabrics dyed with Telon Blue M2R at a 1% dyeing concentration using the conventional method (95 °C, 30 min) and microwave-assisted method (10 min). Washing fastness tests were performed according to ISO 105 C06 B1S method, acidic and alkaline perspiration fastness tests were performed according to ISO 105 E04 method and water fastness tests were made according to ISO 105 E01. Dry/Wet Rubbing Fastness tests were made according to ISO105X12. Fastness properties were evaluated according to ISO 105 A02 and ISO 105 A03 method with grey scale in light cabinet.

Table 9. Fastness Properties (1% Conventional and Microwave Methods).

Dyeing Method	Washing Fastness [ISO105C06 B1S]	Acidic Persp. [ISO 105 E04]	Alkaline Persp. [ISO 105 E04]	Water Fastness [ISO 105 E01]	Dry/Wet Rubbing Fastness [ISO105X12]
Conventional	3/4	4	3/4	4	4/5 - 4
Microwave	3/4	4	3/4	4	4/5 - 4

Table 9. Fastness Properties (1% Conventional and Microwave Methods).

Dyeing Method	Washing Fastness [ISO105C06 B1S]	Acidic Persp. [ISO 105 E04]	Alkaline Persp. [ISO 105 E04]	Water Fastness [ISO 105 E01]	Dry/Wet Rubbing Fastness [ISO105X12]
Conventional	3/4	4	3/4	4	4/5 - 4
Microwave	3/4	4	3/4	4	4/5 - 4

Similar test results were observed in the washing, acidic and alkaline perspiration, water and rubbing fastnesses applied according to ISO standards to fabrics dyed by conventional and microwave methods.

3.4. Role of Microwave Irradiation

Compared to conventional thermal dyeing reported in the literature, the observed dye uptake occurs within remarkably short dyeing times (≤4.5 min). This enhancement can be attributed to the specific effects of microwave irradiation, including:

• Rapid and uniform heating of the dye bath and substrate
• Dipole rotation and ionic conduction effects
• Reduced thermal gradients within the fiber matrix

These factors collectively accelerate dye–fiber interactions and improve fixation efficiency. The experimental results demonstrate that microwave-assisted dyeing enables:

• Fast color development
• High color strength at short processing times
• Efficient utilization of higher dye concentrations

Such characteristics make microwave-assisted dyeing a promising approach for energy-efficient and time-saving textile coloration processes.

4. Conclusions

Comprehensive comparative study was conducted on the acid dyeing of PA-6 fabric, systematically evaluating the performance of conventional heating against the innovative microwave-assisted technique using C.I. Acid Blue 324. This investigated the mechanism of acid dyeing of water 6 (PA6) fabrics, providing a detailed comparison between microwave-assisted heating and conventional dyeing methodologies. The investigation analyzed the influence of key parameters pH, temperature, dyeing time, and dye concentration on the resulting color strength (K/S).

The study confirmed that the conventional dyeing process adheres to established principles, with the highest dye uptake achieved at the most acidic condition (pH 3.0) and the highest temperature tested (95 °C). However, the process is inherently time consuming, requiring a duration of 30 minutes to achieve maximum color yield, which is a significant factor in industrial throughput and energy consumption.

The findings clearly demonstrate that the microwave-assisted method provides a robust scientific basis for developing faster, more energy-efficient, and more sustainable dyeing protocols in the textile industry.

Key Findings are as below.

Effect of pH: In both dyeing methods, the optimum pH value for maximum dye uptake (K/S value) was determined to be 3.0. This confirms the critical importance of an acidic environment to maximize the ionic interaction between the protonated amino groups in the PA6 fiber and the dye molecules.

Conventional Dyeing: In the conventional method, dye uptake increased proportionally with time and temperature, with the highest K/S values obtained after 30 minutes of dyeing at 95 °C. This indicates that the rate-determining step of dye diffusion and fixation is dependent on thermal energy.

Microwave-Assisted Dyeing: The microwave-assisted dyeing method provided a remarkable acceleration in the dyeing time. Thanks to the dielectric heating mechanism (160 W), the time required for dye uptake was drastically reduced compared to the conventional method (seconds instead of minutes).