Introduction

Textile dyeing plant industries produce a significant amount of waste, 5% of which ends up in wastewater effluents of about 637.3 million cubic metres per year, which contributes significantly to the pollution of water bodies1. Wastewater from industries that make dyes and pigments, as well as many others, is typically rich in colour and organic material. The use of dyes is widespread in sectors like textiles, rubber, paper, plastic, and cosmetics. Textiles are the first among these several industries in the use of dyes to colour fibre. Dye discharge from textile industries causes severe air, water, and soil pollution and thus adversely impacts the environment. The textile industry has recently grown to be a significant problem that has an impact on both people and the environment2. Wastewater that contains dye is hazardous because it contains toxic substances, suspended solids, and other chemicals3,4. A chemical that results from their interaction is extremely dangerous for people, plants, and aquatic life. The result is waterborne diseases5. MB is the most common and popular dye in the textile industry, used to colour wool, silks, and cotton. MB is a positively charged anionic quinonoid structure and the chemical formula of MB is C16H18ClN3S. Methemoglobinemia, tissue necrosis, mental confusion, and vomiting are all possible side effects of MB toxicity6. Limiting oxygen transfer and preventing sunlight from reaching water bodies are two negative effects of dyes on the environment7.

Recently, several reports on dye removal methods have been released8. The three main treatment categories for the methods that were presented are chemical, biological, and physical treatments9,10. Some of the remarkable methods that are typically reported include adsorption, biological treatment, electrochemical treatment, advanced oxidation (AOP), and membrane filtration11,12. Pre-proofing is used to get rid of the dye. Each technique has advantages and disadvantages. The approach that is most frequently used is adsorption13. It enables the removal of pollutants at levels ranging from low to high. As a result, numerous studies have been carried out to create adsorbent materials that are efficient and affordable14. The most adaptable and widely used of these techniques is biosorption it is both affordable and user-friendly15,16. Numerous studies have supported and confirmed the use of a variety of materials for pollutant biosorption to remove contaminants17,18. Popular and highly effective biosorbents such as activated carbon are also more expensive19, which has led leading many researchers to search hunt for biosorbents that were inexpensive and easily accessible locally20,21. To remove the dye MB from textile wastewater, T. aestivum is used as a low-cost biosorbent in this study. It is a frequently discarded agricultural waste product that is readily accessible and can no longer be used for beneficial purposes22,23. Additionally, it is freely available or extremely inexpensive, making it a readily available and cost-effective biosorbent. The disadvantages of the synthesized adsorbents for the treatments of the dye wastewater are regeneration of the biosorbent is expensive and results in the loss of materials, require high dosage, and is economically non-viable for some industries like paper and pulp.

Numerous variables, including pH, the amount of biosorbent used, and dye concentration, can affect dye removal by biosorption24. The response surface method is a flexible computational method that can be used to optimise the biosorption process. It is beneficial for planning the modelling and enhancing the optimization of the experiments. It was formerly employed to simulate the biosorption procedure25,26. In this study, we use RSM’s central composite design (CCD) to optimise the biosorption of MB dye on T. aestivum. The proposed study aims to use T. aestivum as an economical and environmentally friendly biosorbent to remove the MB dye from the aqueous sample. The treatment of wastewater from the textile industry has been covered in a few research articles7,27, but most of them describe the current adsorbate in-depth and focus on metals or dyes. They talked about the many low-cost adsorbents available for treating wastewater from the textile industry.

Additionally, combining the RSM with machine learning (ANNs) could increase the reliability of the model. The emergence of better modelling methods with improved model performance, such as ANN, offers a substitute for polynomial regression. The output responses obtained by the CCD were compared to the predictions made by machine learning (ANN) using the MATLAB programme. A closer look at the literature, reveals several gaps and shortcomings. Previous research typically focussed on only investigated the thermodynamics, kinetics, and isotherms study of the biosorption process. These studies warrant a better understanding of biosorption, but there is still a great deal of work to be done along with designing of experiments (RSM) and machine modelling. This article provides a new novel approach to optimization modelling using RSM to investigate and examine how biosorbent dosage, initial dye pH, concentration, and temperature affect the critical behaviour of biosorption. The thermodynamic parameters, isotherms, biosorption kinetics and surface modification of T. aestivum were all determined by analysing the biosorption data using Fourier transform infrared spectroscopy. A schematic diagram of the biosorption study is shown in Fig. 1.

Figure 1
figure 1

A schematic diagram of biosorption study.

Materials and methods

Preparation of T. aestivum biosorbent T. aestivum is procured from neighbourhood vendors and employed in this investigation as a biosorbent

It is first divided into smaller pieces and repeatedly rinsed with water to remove residues any. The biosorbent is then placed and exposed to the sun to dry for one week. The dry biosorbent was then mortar-crushed. Using a sieve shaker, the ground biosorbent is sieved to keep uniform-sized particles, prior to being dried for 24 h in a hot air furnace at 70 °C, the particles that made it through a 250 µm sieve are used deionized water to rinse three times. Biosorption tests are conducted using the prepared biosorbent. The chemical composition of T. aestivum is listed in Table 1.

Table 1 The chemical composition of T. aestivum.

The biosorption procedure is created to recognise biomass activation by employing FTIR spectroscopy to assess the functional groups on the biosorbent surface. With an experimental range of 400–4000 cm−1, the spectra are obtained using a PerkinElmer FTIR instrument.

Preparation of stock solution of MB dye

In this investigation, experimental biosorption is conducted using MB (C16H18ClN3S xH2O) of analytical grade. The characteristic of MB is listed in Table 2.

Table 2 Characteristics of MB.

The requisite quantity of MB dye powder and deionized water are combined to produce the stock solution of MB (500 mg/L). The given concentration levels are produced from the stock MB solution. It was utilised to gather the experimental results.

Biosorption studies of MB on T. aestivum

The biosorption process parameters must be optimised according to variables including the biosorbent dosage, contact time, temperature, pH solution, and initial dye concentration to achieve maximal biosorption. Each experiment involved shaking Erlenmeyer flasks with 100 mL of MB dye solutions at 120 rpm for 60 min. When utilising a pH metre, 1 M NaOH or 1 M HCl solution was added to dye solutions to change the pH. The biosorbent was removed from the mixture using filter paper at intervals of 0.45 µm while stirring. An absorption spectrophotometer (Make: Labman Scientific Instruments Pvt. Ltd., Model: LMSP UV1900) is used to compare the dye concentrations before and after treatment. The means of each experiment's two runs were presented as concentrations. To examine the impact on biosorption kinetics, the test solutions' starting colour density and response time were changed. With the use of a pH metre (Make: HANNA instruments, USA, Model: HI 991001), the pH of the dye solution was changed. To determine how temperature affects different thermodynamic parameters, biosorption research was conducted using diluted HCl or NaOH solutions. Biosorption levels (qt) at time t (mg/g) were calculated using Eq. (1)31

$${q}_{t}= ({C}_{o} - {C}_{t}) V / (W )$$
(1)

Ct (mg/L) indicates the overall dye concentration, Co (mg/L) the initial dye concentration, V the solution volume (L), and W the dry biosorbent mass (g). In order to determine the amount of biosorption at equilibrium, qe(mg/g), was shown in Eq. (2)

$${q}_{e} = ({C}_{o} - {C}_{e}) V / (W)$$
(2)

In this equation, Ce is the equilibrium dye concentration (in mg/L). To respond to the RSM investigation, the dye removal percentage was calculated using Eq. (3)

$$Dye\,removal\,(\%) = ({C}_{o} - {C}_{e})\,/\,({C}_{o}) \times 100$$
(3)

Design of experiments using RSM

Because only one variable is changed while the other variables are kept constant in a standard experiment, the researcher ignores the synergistic effect of the components. A variety of optimization methodologies have been developed in operational analysis over the years, resulting in a long history of optimization studies32. RSM is a methodical statistical methodology that improves the agreement of the minimal test runs when evaluating the relationship between design responses and factors33. The quadrilateral design is provided because the CCD contains only a subset of the experiments required for the five-step factorial and provides schemes with the required statistical properties34,35.

Biosorbent dose (0.5–2.5 mg), initial metal ion concentration (10–50 mg/L), initial dye pH (4–8) and temperature (15–35 °C) make up the design criteria for the CCD of biosorption24. With two chosen as the axial levels, each variable had five levels: 1, 0, + 1, − α and + α. The study's selected independent variables are listed below, and their values and ranges are in Table 3.

Table 3 Codes and levels of independent variables used in the RSM model.

The number of experiments needed for CCD design can be determined by

$$N = 2n + 2n + nc$$
(4)

where c is the number of centre-point replicas, n is the number of numerical components, and N is the total number of experiments25. The graphical analysis, regression analysis, and experimental design were all carried out using software from Stat-Ease Inc. known as Design Expert. A total of 30 trials were designed, each containing six repetitions of the centre points, eight replications of the axial points, and sixteen replications of the cubical points, in accordance with Eq. (4). Regression equations were used to determine the variables' ideal circumstances. Using a four-point combination of four variables and three phases, the maximum organic sorbent dosage, pH, initial metal ion concentration, and temperature were all calculated35. This design was chosen because it met most of the criteria for optimizing bio-absorption studies26. Finding ideal process working conditions to meet performance standards is the primary goal of RSM.

Modelling of the biosorption isotherm

We used the biosorption facts of MB on T. aestivum to solve the isotherm equations. According to the Langmuir isotherm, neither the target molecules nor the adsorbent surface will ever interact. The model also includes a restricted number of energetic websites, which are typically organised in a monolayer36. Langmuir isotherms may be used to simulate the biosorption process.

$$qe= \frac{{q}_{max} bCe}{1 + bCe}$$
(5)

qe is the quantity of dye absorbed at equilibrium in mg and qmax is the maximum quantity of dye that can be absorbed via means of biomass in mg, Ce is the equilibrium MB awareness expressed in mg/L, whilst b is the Langmuir isotherm constant. Instead, the Langmuir equation's linearized form can be shown as follows.

$$\frac{1}{{q}_{e}} = \frac{1 }{{q}_{m}} + \frac{1}{{C}_{e}} {q}_{m}b$$
(6)

Ce denotes for equilibrium concentration of MB (mg/L), qe for the quantity of MB absorbed at equilibrium (mg/g), and qm for maximum/monolayer biosorption capacity (mg/g) respectively. The basic characteristics of the Langmuir isotherm are described by a non-dimensional dissociation constant, RL.

$${R}_{L} = \frac{1 }{(1+ b.{C}_{e})}$$
(7)

Biosorption kinetics modelling

The experimental data on biosorption in this study were optimised using pseudo-first-order. This kinetics study used different dye concentrations (Co = 10, 20, 30, 40, and 50 mg/L) to evaluate the kinetics for five to ninety minutes. The basic description of the biosorption rate determined by biosorption capacity is given below in accordance with Lagergren's first-order rate equation. Typically, a linear expression for this rate is used37.

$$ln \left({q}_{e}- { q}_{t}\right)= ln\,{q}_{e} - {K}_{1}t$$
(8)

The quantities of MB adsorbed on T. aestivum at equilibrium (qe) and at any time (qt), respectively; K1 (min−1) is the pseudo-first-order biosorption rate constant (qt). Ho suggested an expression-based rate-based kinetic model with quadratic coefficients has been put forth for the biosorption of dissociated metal ions (adsorbents) in coal particles. The adsorbent’s biosorption capacity is consistent with this model38. This model is consistent with the adsorbent's capacity for biosorption. The model presents a pseudo-quadratic rate equation and aims to separate the kinetics of the biomass concentration-based quadratic rate equation from the solvent concentration-based data. The pseudo-quadratic model's linear form is as follows in Eq. (9)

$$\frac{1 }{{q}_{t}} = \frac{1 }{{K}_{2}{q}_{e}^{2}}+ \frac{1 }{{q}_{e}}t$$
(9)

T. aestivum absorbs MB dye at equilibrium (mg/g) and at any time, which is designated as qe and qt, respectively. The equilibrium rate constant for pseudo-second-order biosorption is K2. To determine how they would affect Ho's proposed pseudo-second-order model of biosorption kinetics, the test solutions' initial colour density and reaction time were altered.

Biosorption thermodynamics studies

Thermodynamic parameters include entropy (\(\Delta\)S), changes in Gibb's free energy (\(\Delta\)G), and enthalpy (\(\Delta\)H), of biosorption at various temperatures for MB dye onto the T. aestivum29. Five different temperatures were used to investigate the impact of temperature on batch-by-batch tests of MB dye on T. aestivum. The following diagram iillustrate the thermodymanics parameters influences on \(\Delta\)G variation during the biosorption process39. The slope and intercept of the following function were used to calculate the change in entropy and enthalpy during the biosorption process.

$$\Delta G = \Delta H {-} T\Delta S$$
(10)

ANN-based predictive modelling

Few studies have previously used machine learning (ANN) modelling to forecast dye removal of MB performance40. The neurons that make up an ANN are highly coupled processing units that have summing junction and transfer functions. ANN modelling, in contrast to RSM, includes an input (factors), target (experimental response), and output (predicted response). The input layer (representing independent variables), output layer (representing dependent variables), and hidden layers that link inputs with outputs are the layers in which the artificial neurons are placed41. Figure 2 illustrates the pattern of neuronal.

Figure 2
figure 2

Structure of the ANN model for the dye removal % (MB) outputs.

Consent to participate

This research does not involve human participants and/or animals.

Results and discussion

Response surface methodology

The highest dye removal observed and anticipated MB biosorption values, and the matrix of experimental design are listed in Table 4. In 60 min, 30 tests in total were conducted. T. aestivum had the highest dye removal rate (96%) compared to other combinations with 1.5 mg of biosorbent, 10 mg/L dye solution, pH 6, and a temperature of 25 °C. The link between the independent variables chosen and the biosorption of the MB dye is described by regression equations, which are used to express RSM. For this investigation, the regression equation is expressed in terms of coded values is shown as Eq. (11).

$$\begin{gathered} {\text{Dye Removal}} \left( \% \right) = 84.778 + 3.026 * A + - 0.951042 * B + 0.74097 * C \hfill \\ + - 0.843281 * D + 0.150187 * AB + 0.0474576 * AC + - 0.732874 * AD \hfill \\ + - 0.0578228 * BC + - 0.164211 * BD + 0.340879 * CD + - 0.12876 * A^{2} \hfill \\ + 2.29724 * B^{2} + 0.286968 * C^{2} + 0.926208* D^{2} \hfill \\ \end{gathered}$$
(11)
Table 4 Actual value and projected MB removal are included in the experimental design matrix.

A, B, C, and D are the coded variables used in this RSM investigation. To forecast how each element will react to different phases, the equation can be utilised in conjunction with the coded variable. The standard notation for superior and subordinate status is + 1 and 1, respectively. Using this coding equation, the relative effects of the variables are ascertained after comparing the coefficients of the factors. Figure 3 illustrates that the predicted value of MB adsorption is plotted against the actual value from data, yielding an R2 value of 0.9945, which validates the models’ accuracy and can be used in the experiment.

Figure 3
figure 3

The expected values for MB biosorption are plotted against the experimental data.

ANOVA analysis

ANOVA analysis used all the experimental findings for the full factorial response variable that was duplicated at the central and axial points (Table 5). A significant quadratic model contribution is shown in the ANOVA findings in Table 5 with a p-value of less than 0.01. The significant model in the current investigation is shown by the sample F-value of 193.32. This huge F-value may be caused by noise with a mere 0.01% probability. The values obtained using R2 = 0.9945 show a strong correlation between the experimental data currently available and the predicted values of the model put forth to describe the property of the polynomial model. This correlation is described by the calculation of the coefficient, the mean deviation across the model described, and the values themselves. The results with R2 = 0.9945 show that there is a strong correlation between the experimental data that is currently available and the predicted values of the model that is suggested to reflect the property of the polynomial model. The determination of the coefficient, the mean deviation throughout the described model, and the value all demonstrate this link. The value of F is 4.54 shows that there may be a 5.43% risk that the considerable prevalence of Fit F-value deficiency is because of noise, and the absence of Fit is not statistically significant.

Table 5 ANOVA for biosorption of MB removal.

Response surface plots show the MB biosorption efficiency (%) response to common parameters based on most values of alternative parameters for a certain set of components is shown in Fig. 4a–f. These 3D plots' curves demonstrate how the process variables interact. The optimum scenario and interacting outcomes of the four evaluated factors are shown in the 3D aspect plots in Fig. 4a–f.

Figure 4
figure 4

MB biosorption by T. aestivum biomass in a three-dimensional surface plot, illustrating the interactive effects of the four factors under test.

Effect of biosorbent dose

The availability and cost of biomass are the main deciding considerations when adopting it for large-scale industrial purposes. Biomass is one of the most exciting categories of biosorbents39. In terms of getting rid of heavy metals from wastewater, agricultural biomass has a whole lot of benefits, which include being a cost-powerful renewable natural biomass, having an excessive metal elimination efficiency, having an excessive ability for absorption, and being capable of regenerating and reusing the biomass42. Figure 4d demonstrates that the removal effectiveness of MB increases with increasing biosorbent dose and declines with decreasing dye concentrations. The primary cause for the simultaneous rise in MB's biosorption capability and an increase in biosorbent concentration is the availability of many more open active sites on the surface of the biosorbent43. On the other hand, Vijayaraghavan et al. discovered that the concentration of T. aestivum biomass increased together with the rate of MB biosorption from an aqueous solution44. The reality that the dye's biosorption per cent decreases as biomass attention increases demonstrates that the wide variety of dye molecules required to absolutely cowl all the lively adsorption sites in the biomass at excessive sorbent doses is insufficient1.

Effect of MB concentrations

The relationship between the biosorbent dose and the concentration of MB dye is shown in Fig. 4a. The MB removal percentages increase with the increase of biosorbent dose and dye concentration. The biosorption process is also influenced by the initial MB concentrations. Growing the preliminary dye concentrations usually causes growth within the elimination percentage. The biosorption quantity of dye on the surface of adsorbents increases as the initial concentration of MB increases45.

Effect of initial pH

The biosorption procedure may be motivated with the aid of using numerous variables, along with pH, preliminary concentration, and biosorbent dosage. Figure 4c describes the association between the pH and the temperature. While the initial pH level, MB concentration, and contact duration were retained at their zero levels, the three-dimensional surface plots (3D) in Fig. 4c show the simultaneous effects of pH and temperature on MB removal (%), respectively. The process of contaminant biosorption has been discovered to be most affected, among other things, by the initial pH level. pH levels influence a variety of processes, including the chemistry of metal solutions, the activity of functional groups in biomass, and the net charge on the surface of sorbent cells. Heavy metal ions and H+ may compete with one another for cellular active sites on the surface of biosorbent cells since the biosorption method for significant metals is usually potential of hydrogen ion concentration dependent46. According to the study of experimental findings, the T. aestivum biomass can more efficaciously soak up the MB dye because the pH rises, with maximum biosorption happening at approximately pH 8. The T. aestivum surface appearing as a biosorbent and the protonation and deprotonation of the MB dye can each be used to provide an explanation for the outcome.

Effect of temperature

The biosorption process sensitivity to temperature can be used to determine a biosorbent sorption capacity. The impact of temperature on the removal of Basic Blue 41(BB41) through effective microorganism-primarily based total leaf compost was assessed at various temperatures between 25 and 45 °C47. The outcomes of the experiment showed that a rise in temperature would result in a greater capacity for dye sorption (Fig. 4b). Figure 3e demonstrates that the slightly increasing the concentration at lower temperature the efficiency of dye removal also increases. Researchers have found that increasing temperatures increase the rate of solute diffusion, which has a significant impact on the sorbent's ability to absorb solutes48. However, the impact of temperature on biosorption is quite delicate and might be slightly increased at lower temperatures. The ability of the dye molecules to sustain contact with the biosorbent surface sites and the expansion of pore size with rising temperature were cited as the causes of this outcome. In general, a rise in temperature accelerates the rate of solute diffusion, which has a significant impact on the ability of biosorbents to bind to solutes48.

Isotherms model for biosorption

A fitting result of a linear line with a (Ce/q) intercept to the Langmuir equation is displayed as (Ce/q) versus (Ce) shown in Fig. 5A. According to Table 6, The Langmuir isotherm's determined correlation coefficients were 0.9381. The biosorption's deviation from linearity is considered when calculating the second Langmuir constant, RL. In the current investigation, the equilibrium value of the dimensionless factor value, RL, which ranges from 0 to 1, was 0.062 (Table 6), indicating favourable biosorption. That confirmed that T. aestivum and MB had favourable biosorption (Fig. 5A).

Figure 5
figure 5

(A) Langmuir isotherm model and (B) Freundlich isotherm in linear form.

Table 6 Parameters of Isotherm models of MB onto T. aestivum.

Figure 5B illustrates the values of 1/n and Kf determined from the intercept and slope of the linear plot of ln qe versus ln Ce49. The desired constants are provided with the regression equation as shown in Table 6. The favourable nature of biosorption was proved by the fact that n is between 0 and 150. The Langmuir and Freundlich biosorption isotherms best explain the equilibrium results, demonstrating that monolayer formation mediates biosorption on a homogeneous surface. Figure 5B shows a linear fit of the Freundlich equation using a line with an intercept of ln Kf and a slope of n49.

Kinetic studies

The first-order kinetics' calculated K1, qe, and R2 values are shown in Table 7. As shown in Fig. 6, pseudo-second-order graphs were made by plotting t/qt vs. time. The second-order rate constants have been calculated using the charts. The second order's calculated K2, qe, and R2 are supported by Table 7.

Table 7 Kinetic models of pseudo first and second order.
Figure 6
figure 6

Pseudo second order kinetic curve for MB elimination% by T. aestivum.

Pseudo-second-order kinetics' correlation coefficients are becoming close to unity in contrast to pseudo-first-order kinetics. Therefore, it is evident that the pseudo-second-order model represents a biosorption that is more successful.

Thermodynamics study

As expected, the biosorption capacity of MB onto T. aestivum increases substantially while the temperature rises from 20 to 40 °C. The biosorption capability of T. aestivum is boosted through the biosorbent’s expanded pore length and the warming of the sorbent's surface. Raising the temperature causes the big dye molecule to penetrate more deeply, which also enhanced the large dye ion's potency, which lessens the impact of swelling16,51. As a result, MB was able to absorb the T. aestivum more quickly at high temperatures. Gibbs free energy (\(\Delta\)G), enthalpy (\(\Delta\)H), and entropy (\(\Delta\)S), among other thermodynamic characteristics, have all been calculated for the extrusion28. Furthermore, Table 8 also provides \(\Delta\)H, \(\Delta\)G, and \(\Delta\)S values for 20 mg/L preliminary MB dye concentrations.

Table 8 Parameters for the thermodynamic removal of MB from T. aestivum.

The negative values of ΔG demonstrated the spontaneity and viability of the adsorption process for MB sorption on T. aestivum. Because there is less unpredictability at the solid/liquid interface when MB is adsorbing to T. aestivum, the value of entropy ΔS (− 10.11 kJ/mol K) is negative. The negative value of ΔH (− 12,300.04 kJ/mol for MB) supports the exothermic character of the reaction. Good interaction between T. aestivum and MB is indicated by high levels of ΔH. This led us to the conclusion that the sorption of the dye in T. aestivum is a process of chemical biosorption.

Sticking probability

The sticking probability (S*) is a function of the adsorbate/biosorbent system under discussion, but it is temperature dependent and needs to fulfil the criterion 1 < S* < 1 for optimum biosorption. The value of sticking probability was calculated from experimental data. It was calculated using a modified Arrhenius- type equation.

$$S^{*} = \left( {1 - \theta } \right)e_{ RT}^{ - Ea}$$
(12)

The parameter S* represents the measure of an adsorbate’s capability to persist on the adsorbent indefinitely. The surface coverage (\(\theta\)) at different temperatures was calculated to assess the effects of temperature on the sticking probability over the temperature range from 288 to 308 K. The slope and intercept of the ln (1 − ϴ) against 1/T plot can be used to determine the value of Ea and S*. The negative value of Ea shows that methylene blue dye removal by adsorption onto Triticum aestivum is favoured by a lower solution temperature, and the biosorption process is exothermic in nature. This biosorbent has affinity for methylene blue, indicating that it is a superior biosorbent for removal of methylene blue, as shown by MB sticking probability of S* < 1 on the surface of biomass is presented in Table 8.

Artificial neural networks (ANNs) modelling

ANNs are used to generate new processes, analyse existing ones, and anticipate the result and performance of systems26. The feed-forward neural network's optimal topology consists of an output layer, a hidden layer, and four neurons each in the input and hidden layers (including one neuron).

The experiments designed by the CCD provided the input and output for training. After training, a neural network’s weights and biases are displayed in Table 9. The model’s logsig (log-sigmoid) transfer function provides the necessary information for anticipating the outcomes. Figure 7 displays the expected values of the ANN model. In terms of the number of learning epochs, Fig. 8 analyses the ANN model's training, validation, and tests.

Table 9 Network weights and biases using the optimal parameters for the ANN model.
Figure 7
figure 7

Regression plot for ANN of MB on T. aestivum training, validation, and prediction test.

Figure 8
figure 8

Performance of training, validation, and test error for ANN of MB on T. aestivum.

The RSM- predicted improved process conditions are also assessed using an ANN model. Biosorbent dose (2 mg), dye concentration (20 mg/l), dye solution pH (7) and temperature (20 °C) are used as input parameters for the ANN model. When the test error is lowest and the mean squared error has not changed for at least 1000 iterations, the training is terminated. The network is trained in this analysis for a total of 6 epochs. When the anticipated values from the ANN and RSM models are compared, it becomes evident that the values predicted by both models are considerably closer to the experimental results (Table 9).

Multiple response optimization

The experimental findings were optimised using Design-Expert software35. The 93.51% biosorption efficiency was attained under the ideal conditions shown in Table 1025 and conducted a special batch experiment to demonstrate optimization under ideal circumstances for comparison under suitable circumstances between projected and actual results. The difference between the projected value and the actual value is 93.90% or 93.51% confirming that the anticipated and actual values are the same, yielding verified model results. According to the requirements listed in Table 10, model equation is developed to maximise MB removal efficiency. Predicted numerical optimization was obtained 2 mg biosorbent dose, 20 mg/L concentration, 7 pH and at 20 °C temperature with 93.90% MB dye removal efficiency. The percentage error between RSM prediction and optimized condition is 0.41% and error between RSM and ANN is 2.17%. Validation experiment conducted as same input value gave 93.51% MB removal efficiency & projected reactions are consistent with model predictions validated under these ideal process condition (Table 10).

Table 10 RSM and ANN predictions optimization conditions for multiple responses.

Characterization of biosorbent

Surface modification analysis by FTIR

Using FTIR spectroscopy, surface alteration may be found, allowing the biosorption mechanism to be examined. Using the Perkin Elmer FTIR system, the FTIR spectrum data was Gathered. The surface of the biosorbent is visible with functional groups such as nitro, hydroxyl, carbonyl, carboxylic, phenol, and phenol groups in Fig. 9. FTIR spectra can be used to distinguish between the many functional groups that are present in biosorbent formations52. Two distinct peaks at 1372 and 1371 cm−1 and 1512 and 1511 cm−1, respectively, indicate the stretching vibration of the nitro-N–O groups, which were discovered to have been extended due to biosorption on biosorbent. The 1634 and 1632 cm−1 peaks are the stretches of C=C. The C–O stretch of various moieties and the carboxylic group have been implicated as the cause of the numerous strong, sharp peaks that were observed between the levels of 1100 and 1330 cm−124. The hydroxyl functional group's O–H stretching vibration and the band at 3200–3600 cm−1 had previously been linked (Fig. 9). The stretching of the carboxyl groups in C=O is responsible for the peak around 1700–1800 cm−1. The surface charge differential may change due to positive or negative surface charges depending on the pH of the solution2,6,53. In a solution with a lower pH value, the system will operate more frequently and develop a positive surface charge. The hydroxyl group is indicated by the height increase at 3340 cm−1 caused by the MB absorbed on T. aestivum, as well as by the prolonged robust sharp top at 1034 cm−1. Peaks in the range of 1327–1372 cm−1 were caused by the interaction of MB and Nitro companies in T. aestivum54,55,56.

Figure 9
figure 9

FTIR spectroscopy for T. aestivum biosorption of MB.

SEM evaluation

The surface topography and properties of T. aestivum can be directly scanned using a scanning electron microscope (SEM) examination. SEM images are displayed Before and after MB biosorption, the biomass of T. aestivum (Fig. 10A,B). The biomass made of untreated T. aestivum had a rough and irregular surface, as seen in Fig. 10A. The look of fresh, shining particles absorbed on the surface of T. aestivum was depicted in Fig. 10B. Another distinguishing quality had been demonstrated (Fig. 10B). The surface area of polymeric T. aestivum has been reduced due to possible cross-linking between positively charged ions and negatively charged chemical functional groups in the cell wall. The surface of T. aestivum is rough and undulated, which increases the surface area exposure of the active biosorption sites and leads to MB's enhanced bio-absorption efficacy.

Figure 10
figure 10

SEM images illustrated T. aestivum biomass: (A) before and (B) after MB biosorption.

Conclusion

The biosorption of MB dye onto T. aestivum was demonstrated in this work using the experimental variables of biosorbent quantity, dye pH, temperature, and concentration. The experimental result of the biosorption performance of MB was examined and found to be superior to the use of the CCD-primarily based RSM optimization technique and ANN. Using isotherms, kinetics, and thermodynamics studies, the best RSM results were examined. This study assessed T. aestivum ability to remove MB dye from wastewater. The experimental results were demonstrated to be closely related to the Langmuir isotherm model, which has a maximum biosorption capacity of 0.36 mg/g. Additionally, MB sorption on T. aestivum was studied using pseudo-second-order kinetics at a rate constant of (2.56 gmg−1 min−1). Thermodynamic analysis shows that the adsorption process is exothermic and spontaneous. After characterising the biosorbent by evaluation of the T. aestivum FTIR spectra, it was determined that the change of dye ions with counterions, which are typically attached to the surface through carboxyl, hydroxyl, and nitro groups, is the mechanism behind the metal binding. T. aestivum is a more affordable alternative adsorbent even if compared to commercial activated carbon, it has a higher capacity for biosorption. The use of T. aestivum as an adsorbent to take the colour out of water could be inexpensive and efficient.