Adsorptive removal of acid red 18 dye from aqueous solution using hexadecyl

Scientific Reports volume 13, Article number: 13833 (2023) Cite this article

136 Accesses

Metrics details

Discharging untreated dye-containing wastewater gives rise to environmental pollution. The present study investigated the removal efficiency and adsorption mechanism of Acid Red 18 (AR18) utilizing hexadecyl-trimethyl ammonium chloride (HDTMA.Cl) modified Nano-pumice (HMNP), which is a novel adsorbent for AR18 removal. The HDTMA.Cl is characterized by XRD, XRF, FESEM, TEM, BET and FTIR analysis. pH, contact time, initial concentration of dye and adsorbent dose were the four different parameters for investigating their effects on the adsorption process. Response surface methodology-central composite design was used to model and improve the study to reduce expenses and the number of experiments. According to the findings, at the ideal conditions (pH = 4.5, sorbent dosage = 2.375 g/l, AR18 concentration = 25 mg/l, and contact time = 70 min), the maximum removal effectiveness was 99%. The Langmuir (R2 = 0.996) and pseudo-second-order (R2 = 0.999) models were obeyed by the adsorption isotherm and kinetic, respectively. The nature of HMNP was discovered to be spontaneous, and thermodynamic investigations revealed that the AR18 adsorption process is endothermic. By tracking the adsorption capacity of the adsorbent for five cycles under ideal conditions, the reusability of HMNP was examined, which showed a reduction in HMNP's adsorption effectiveness from 99 to 85% after five consecutive recycles.

Today’s unstoppable industrial growth will inevitably lead to various environmental issues due to the chemical compounds they use1,2,3,4,5,6. Synthetic dyes are among these compounds, one of the most important industrial substances6,7. Azo dyes are regarded as the primary class of synthetic dyes (60–70%) and are extensively employed in a variety of industries, including textile, food, rubber, plastic, paper, and cosmetics Azo dyes are regarded as the primary class of synthetic dyes (60–70%) and are extensively employed in a variety of industries, including textile, food, rubber, plastic, paper, and cosmetics7,8,9. These dyes are formed by an azo group (–N=N–)8, low cost, highly stable and soluble9. Discharging untreated dye-containing wastewater gives rise to environmental pollution, leading to photosynthesis disturbance by preventing sunlight penetration10. Several biological processes can be easily stopped with the presence of dyes in water11. It is essential to highlight that ingesting these dyes results in cardiovascular shock, cancer, mutagenesis, teratogenesis, vomiting, gastrointestinal discomfort, diarrhoea, etc12.

From this fact, it can be apparent that dye-containing wastewater treatment is a major challenge. Many researchers have investigated several physical, chemical and biological methods for treating coloured wastewater, such as membrane filtration, advanced oxidation techniques, ion exchange, chemical precipitation, coagulation, and flotation13,14. However, many of these procedures are unreliable since they fail to remove the colour sufficiently. They are ineffective for dye removal due to their high investment costs, lack of selectivity, and difficulty in regeneration14,15.

Adsorption has proven to be an effective technique compared to other methods due to its simplicity of use, high efficiency, and low energy need technology16,17. Researchers have recently evaluated pumice stones as a cost-effective adsorbent in water and wastewater purification procedures17,18. Pumice is a volcanic, light, porous and nontoxic stone19. Open channels inside its structure permit ions and water to enter and exit the crystal lattice20. It is a valuable scouring, scrubbing, and polishing material in powdered form and as a pumice stone21. Different agents have been used to modify adsorbents to improve their adsorption capacity; various pumice modifications were tested in previous studies. Pumice modification effectively removes phosphate ions from water22. Iron-coated pumice was a promising adsorbent in removing NOM from water23. Magnesium chloride and hydrogen peroxide were used to modify the surface of natural pumice to increase the adsorbent's specific surface to remove fluoride24. Pumice modification by acid increased the adsorbent efficiency in humic acid removal from water25.

This study's major goal was to use a low-cost adsorbent for water purification using a locally plentiful adsorbent. Even though there has been earlier research on the removal of dye compounds using pumice stone, the present study stands out because it uses nanosized pumice to examine how the increased surface area of the pumice affects the adsorption process. Therefore, the use of a modified nano-scaled pumice as a novel adsorbent for dye compound treatment from water was studied in the present research. Response surface methodology (RSM) with central composite design (CCD) was also employed to ascertain the relationship between the effectiveness of dye removal and certain factors and optimize the adsorption process.

The use of HMNP as an adsorbent for removing AR18 from aqueous solutions was investigated. All tests were conducted on a lab scale, and the effect of different parameters such as pH, adsorbent dose, contact time and initial dye concentration were examined.

Alvan Sabet Company, Hamedan, Iran, provided AR18 dye. All other chemicals like hexadecyl trimethyl ammonium chloride, Sodium hydroxide (NaOH, 1N) and hydrochloric acid (HCl, 1N) were purchased from Merck (Darmstadt, Germany).

Experiments were carried out with 25 ml of dye solution at different concentrations. pH adjustment was done using NaOH and HCl 0.1 N. Samples were contacted with a desirable amount of adsorbent (0.5–3 g/l) on a shaker with 200 rpm at room temperature and a certain contact time. After adsorption, samples were centrifuged at 4500 rpm for 10 min. The studied variables in the present research were pH (3–9), adsorbent dosage (0.5–3 g/l), contact time (10–90 min) and initial dye concentration (10–70 mg/l). The amount of adsorbed dye was calculated by using the mass balance Eq. (1):

where C0 and Ce are the initial and final concentration of dye (mg/l), M represents the mass of adsorbents (g), and V is the volume of AR18 solution (L).

To determine the pH point of zero charge (pHZPC) for HMNP, 0.2 g/L of the adsorbent in 30 ml of NaCl solution (0.01M) with different initial pHs (2–4–6–8–10–12) was shaken for 24 h. then the final pH of the solutions was measured and plotted versus initial pHs. The pH in which the curve crosses the line (final pH = initial pH) is taken as the pHzpc26.

To obtain demanded concentration of AR18 (10–70), the first stock solution was prepared by dissolving 0.5 of dye in 1 L distilled water and other desirable concentrations were prepared from the stock solution. Concentrations of dye solution were read at λ = 507 (nm) using a UV–visible spectrophotometer (Perkin Elmer Lambda 25) (Fig. 1).

AR18 Calibration Curve.

The pumice stone came from Iran's province of Azerbaijan. In the mineral processing lab at the mineral processing laboratory, school of mining engineering college, campus university of Tehran, Tehran, Iran, the raw pumice stone was crushed using a rad mill to a size of 100 mm. After that, a planetary ball mill transformed powdered pumice into Nano-pumice. At the central lab, Amirkabir University of Technology, Tehran, Iran. Nano-pumice was first thoroughly cleaned with distilled water; after that, the surface porosity was increased by contacting the adsorbent with a 1N HCL solution for 48 h at room temperature. The adsorbent was then fully washed with distilled water to achieve effluent turbidity of less than 1 NTU and a pH of 7, and the pumice was then dried in an oven at 105 °C for eight hours.

Nano-pumice was modified with a cationic surfactant hexadecyl-trimethyl ammonium-chloride (HDTMA. Cl) (2.5 mmol) solution. pH was adjusted to 10 by adding NaOH 1N, then shaken for 10 h. at room temperature at 220 rpm. After this time, filtered and dried at 120 °C for 2.5 h., then washed with distilled water and again dried at 120 °C for 6 hr27.

Field Emission Scanning Electron Microscope (FESEM) was used to assess the surface morphology of Nano-pumice. TEM photograph was applied to determine the particle size. The specific area and mean pore diameter were determined by BET, XRD, XRF, and FTIR were also used for more adsorbent analysis.

Isotherm studies were performed under optimum conditions with different dye concentrations (25–70mg); the added adsorbent to each sample was 2.375 g/l with solution pH = 4.2, and then samples were shaken at 200 rpm for 70 min. Kinetic studies with optimized parameters were conducted at contact time in the 10–70 min range. To determine dye adsorption on HMNP, three kinetics models and four isotherm models were examined.

The Thermodynamic of AR18 adsorption on HMNP was evaluated at optimum conditions (pH = 4.5, adsorbent dose = 2.375 g/l, contact time = 70 min, initial AR18 concentration = 25 mg/l) and different temperatures (15–55 °C) to find the performance of adsorption process. Thermodynamics parameters of adsorption were assessed by Gibbs free energy changes (ΔG0), enthalpy changes (ΔH0) and entropy changes (ΔS0) and sticking probability (SP*)[Eqs. 2–5]:

where Ea. is the activation energy (kJ/mol), T is the temperature (K), K is the sorption equilibrium constant, and β is surface coverage.

Experiments were designed using Design-Expert11 (Stat. Ease.Inc Minneapolis, USA) software with Response Surface Methodology (RSM). A central composite design was applied to evaluate the effect of 4 different variables on the adsorption process (pH, initial concentration, contact time, and adsorbent dosage). CCD requires centre points, axial points, and cube points. The total number of experiments can be determined by presented Eq.(6)

K represents the number of experimental variables, 2k is the cubic runs, 2k is the axial runs, and C0 is the centre point's runs. Table 1 presents independent variables and the levels of each variable, while CCD and coded factor values are shown in Table 2.

X-ray diffraction of pumice was analyzed in the range of 2θ = 5–80° and step size = 0.02; the result is shown in Fig. 2. Major constituents of Nano-pumice are Anorthite (CaAl2Si2O8), Quartz (SiO2), Hematite (Fe2O3) and Hornblende (Ca, Na)2(Mg, Fe, Al)5(Al, Si)8O22(OH)2). The main peaks were observed at 2θ = 10.60°, 22.06°, 23.78°, 24.48°, 26.51°, 28.10°, 30.33° and 35.64°28,29,30. A dome at 2θ = 20–40° can confirm the more amorphous phase of Nano-pumice31. The presence of Quartz in this analysis shows good agreement with the high percentage of SiO2 in the sorbent, as reported in Table 3.

XRD of Nano-pumice.

X-ray Fluorescence Analysis was done to determine the chemical composition of pumice (Oxford Instruments, ED2000). The results are given in Table 3. As can be seen from the results, SiO2 and Al2O3 are the two main compounds in the Nano-pumice sample.

While HMNP has become more agglomerated with a smooth surface and is extremely porous, showing more accessible sites for dye adsorption (Fig. 3b), NP exhibits sharp edges and a rough surface texture in FESEM images (Fig. 3a). The image taken following the adsorption procedure demonstrates how dye molecules filled the pores and surfaces of the HMNP. (Fig. 3c). Particle size can be understood from the TEM image of nano pumice in Fig. 4, and it is also clear that the particles are agglomerated and have a semi-polygonal form.

FESEM images of Nano-pumice [(a) (NP), (b) (HMNP), (c) (after adsorption HMNP)].

TEM of Nano-pumice.

Elemental constituent of HMNP material determined by Energy-dispersive X-ray spectroscopy (EDX). From the results in Fig. 5, it is obvious that the major contents are Si and oxygen, with 42.3% and 41.7%, respectively; other elements are Al, Fe, Ca, K, and Cl.

Energy-dispersive X-ray spectroscopy of HMNP.

BET (Microtrac Bel Corp, BElSORP Mini) analysis (N2 gas adsorption method) was used to calculate total pore volume, specific surface area and average pore diameter of NP and HMNP. The results of BET are shown in Table 4. The increased surface area by modification of Nano-pumice (from 1.49 to 10.27) is aligned with previous studies32,33. The pore size distribution calculated by the BJH method is displayed in Fig. 6. As it can be seen, HMNP pore size distribution is between 1 and 100 nm, and most of the particle's pore sizes are 2–50 nm which shows the mesoporous size of the sorbent.

HMNP pore size distribution.

To obtain the functional groups of the pumice sample, the Fourier transform infrared analysis was performed (PerkinElmer, Spectrum Two) while the analysis range was between 400 and 4000 cm−1. Figure 7 shows the FTIR spectra of NP, HMNP, and after adsorption, HMNP Peaks at 3415–3423 cm−1 were related to water molecules 18. 1049 cm−1 and 1060 cm−1 have appeared in NP, HMNP and after adsorption HMNP, which are related to Si–O and Si–Al stretching vibration 34. 1625–1641 cm-1 showing stretch vibration of band O–H. Si–O–Al band was located at 779–786 cm-1 while near 466 cm-1 bending vibration of the Si–O–Si band was identified23. The band around 587–621 cm-1 is associated with the bending vibration of Fe–O320. In HMNP and after adsorption HMNP, two new peaks were observed at 2928 and 1384 cm-1 related to C–H band and C=O, respectively35,36. The peak at 2033 cm-1 found after adsorption of HMNP may be due to the C–O bond.

FTIR of Nano-pumice.

The validity of linear, 2FI, Quadratic and Cubic models was assessed. The Quadratic model was selected with an insignificant lack of fit (0.6656), confirming that the model is valid with Adjusted R2 = 0.9898 and Predicted R2 = 0.9787. Data for all fitted models are shown in Table 5. As can be seen from Table 6, different variables have their effects on dye adsorption. In this study, initial dye concentration showed the most impact on dye adsorption efficiency with an F- value of 1354.54.

On the other hand, time had the lowest effect. Also, the interaction between A and C significantly affects adsorption due to its bigger F value among all other interaction variables. The quadratic function of D also showed the highest effect on dye adsorption compared with three others (A2, B2, and C).

Figure 8a displays predicted vs. actual efficiency in AR18 removal from solution by HMNP, which shows a good correlation between obtained experimental efficiency and predicted efficiency by software. In Fig. 8b, the residual amount of each run is shown, indicating a small difference between them (the highest and the lowest amounts were between 2 and − 2).

Predicted vs. actual value of AR18 removal (a) residual vs. the run (b).

According to Fig. 9a,c and the negative coefficient of pH, dye removal effectiveness declines as pH rises. AR18 adsorption increases dramatically at pH < 4.2 but gradually at pH > 4.2. The existence of more surface positive charges on the adsorbent at lower pHs and negative charges on the dye molecules, and the resultant electrostatic sorption between them, can be used to explain why AR18 removal is higher at acidic pHs37. The calculated pHZPC value for HMNP was 5.6. It implies that the sorbent's surface is positively charged when the pH of the solution is lower than pHZPC, and adsorbent surfaces become negatively charged at pH levels above pHZPC value, which causes dye ions to repel one another and reduce AR18 adsorption. Whereas at pH = 5.6, surface charges are zero38. As seen from Fig. 9a,c, increasing the adsorbent dosage increased the effectiveness of dye removal. On the other hand, adding more HMNP (0.5–3 g/l) increased the adsorption efficiency. It is most likely because more sites for dye adsorption can be provided with higher dosages. This outcome is consistent with earlier research39.

2D and 3D and contour plots showing the effect of pH and adsorbent dose (a, c), initial concentration of AR18 and time (b, d).

In Fig. 9b, d, The removal efficiency increases from 40 to about 100% as the initial concentration of AR18 decreases, particularly from 45 to 10 mg/l. It also increases when the sorbent has more time to contact the dye molecules, from 10 to 90 min. In the time range of 10–90 min, the impact of contact time was examined. It was discovered that as the contact time grew, more dye was absorbed. It makes sense that as the amount of time increases, more dye molecules have a chance to adsorb on the surface of the HMNP. This result is in agreement with other studies40. Initial dye concentration is the primary factor affecting the effectiveness of dye adsorption and significantly impacting the absorption rate. Initial dye concentration has a reverse effect on dye removal. While the initial concentration increases, dye removal decreases. A possible explanation is adsorbent's free sites are occupied when the concentration is high41.

CCD was used for the development of mathematical equations. The highest efficiency was 99%. The final equation shows the empirical relationship between dye removal (Y) based on pH (A), dosage (B), time (C) and initial dye concentration (D):

Insignificant terms (p values > N 0.05) were dismissed for the Development of the regression model equation:

Using the numerical optimization method from software, the maximum efficiency (Eff = 99%) was determined to occur at pH = 4.5, adsorbent dose = 2.375 g/l, contact time = 70 min and initial AR18 concentration = 25 mg/l. But the best AR18 removal efficiency was achieved at 98.8% in practice with the mentioned conditions.

To realize the nature of the interaction between dye molecules and HMNP adsorption isotherms is necessary42. In the present study to model the relationship between adsorbed dye on the adsorbent and remained dye in solution, Langmuir, Freundlich, Temkin and Dubinin-Radushkevich models were used (Their plots are shown in Fig. 10), obtained parameters and constants are shown in Table 7. Isotherm models give a better understanding of the adsorption mechanism. To carry out isotherm’s studies, all parameters were at their optimized conditions with pH = 4.5, adsorbent dose = 2.375 g/l, contact time = 70 min and initial AR18 concentration in the range of 10–70 mg/l at room temperature. To corroborate the fitted model, the correlation coefficients were used.

Isotherm models for AR18 adsorption: (a) Langmuir (b). Freundlich (c) Temkin (d) Dubinin-Radushkevich.

Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich are expressed by following equations (Eqs. 7–10) respectively in Table 8. Langmuir model is valid for the monolayer adsorption of a liquid on a homogenous adsorbent surface43. Where qmax (mg/g) is the maximum adsorption capacity of the adsorbent, Ce is defined as equilibrium concentrations, and b is the adsorption rate constant related to the energy of adsorption (l/mg), the larger b value depicts a larger affinity of adsorbent to the pollutant44. From obtained data, the maximum sorption capacity and adsorption energy for HMNP were 12.84 mg/g and 2.64 l/mg, respectively. Additionally, the high b value (2.64) points out the strong binding of AR18 on the HMNP surface.

Freundlich model uses for adsorption on heterogeneous surfaces with the interaction between adsorbed molecules and describes heterogeneous systems45. KF is the Freundlich constant (l/g) is the adsorption or distribution coefficient, and the 1/nF value indicates the degree of non-linearity between solution concentration and the adsorption process46. Furthermore, 1/nF > 1 demonstrates cooperative adsorption, while 1/nF < 1 implies a normal Langmuir adsorption47. The result of experimental data from the Freundlich model showed 1/nF > 1 (0.159), which reveals that the adsorption process of AR18 removal follows a normal L-type Langmuir adsorption. Besides, the coefficient 1/n (generally 0–1) indicates the favourable adsorption of the adsorbate to adsorbent42. Temkin isotherm model considers the effects of indirect adsorbent–adsorbate interaction on adsorption isotherms and heat of adsorption42. BT = (RT)/bT, T is the absolute temperature (Kelvin), R is the universal gas constant (8.314 J/mol K), b is the heat of adsorption constant, and AT (L/g) is the binding constant46.

The D–R isotherm model is used to identify the nature of the adsorption process as physical. Where ϵ is Polanyi potential, β is a constant for the free energy of adsorption48. The affinity between AR18 and HMNP can be estimated by the RL constant, which is dimensionless.

b (L/mg) is the Langmuir constant and C0 (mg/L) is the AR18 concentration. The value of RL shows the nature of adsorption as follows49:

0 < RL < 1 favorable, RL > 1 unfavorable, RL = 1 linear, RL = 0 irreversible.

The calculated RL value is between 0.003 and 0.03. As all of these values are 0 < RL < 1, it can be understood that pumice has favourable adsorption.

In this study, Langmuir had a greater R2 value than other models, and it was obtained at 0.9962; for D-R, this value was 0.85; for Temkin, it was 0.71, and for Freundlich, it was 0.64, which means that the adsorption isotherms are in good agreement with Langmuir model and AR18 sorption on HMNP is a monolayer. Table 7 displays isotherm model parameters and constants for AR18 removal by HMNP.

Kinetic studies were conducted to understand the adsorption mechanism and dye uptake rate. Pseudo-first-order, Pseudo-second-order, and Intra-particle diffusion models were used to analyze the adsorption kinetics and Eqs.11–13 present models, respectively (Table 8) in which qe (mg/g) is the amount of adsorbed dye on the adsorbent at equilibrium conditions, qt (mg/g) is the amount of adsorbed dye at any time. K1 (min−1), K2 (g/mg.min) and Kdif (mg/ g·min0.5) are the rate constants of pseudo-first-order, second-order and Intra-particle diffusion models, respectively. In this study, Pseudo-first-order describes the uptake rate based on adsorption capacity. The obtained data didn’t align with this model due to its low qe compared to the calculated qe and the low R2. The R2 value for the Pseudo-second order was obtained at 0.999, revealing that the adsorption process is best fitted into this model. Furthermore, the calculated qe value in the Pseudo-second-order model (qe cal = 10.834 mg/g) is closer to the experimental qe value (qe exp. = 10.36 mg/g). These results are in agreement with Gomez50 Kuczajowska-Zadrożna51 and Zhang52. The rate of adsorption site occupation is assumed to be proportional to the square of the number of empty sites by pseudo-second-order kinetic theory. Table 9 displays Kinetic model parameters and constants for AR18 removal by HMNP, and Fig. 11 represents kinetic model plots.

Kinetic Models for AR18 adsorption: (a). Pseudo-first order (b). Pseudo-second order (c) Intraparticle diffusion.

Temperature is an important parameter in the adsorption process. Thermodynamic studies were carried out at five different temperatures to understand the effect of temperature on dye removal efficiency. Table 10 indicates that increasing temperature increase k and qe, which suggests that AR18 removal by HMNP can have higher efficiency at a higher temperature. The obtained values of Gibbs free energy changes (ΔG0), enthalpy changes (ΔH ͦ) and entropy changes (ΔS ͦ ) are presented in Table 10. ΔH0 has a positive value (33.59 (kJ/mol)), meaning the adsorption process is endothermic. In other words, by increasing temperature, the removal efficiency increases since heating the active sites of adsorbents to high temperatures strengthens the bonds between the adsorbate molecules. Negative ΔG0 (between -1.978 and -6.938 kJ/mol) indicated the spontaneous nature of dye removal. The positive amount of ΔS° (0.117 kJ/mol) can ascertain the increased randomness at the solid/liquid interface53. These results are in agreement with previous studies54.

Ion exchange, physisorption, and chemisorption are the three main divisions of the adsorption mechanism. The term "physisorption mechanism" refers to surface adsorption that doesn't interfere with the adsorbent's electronic orbitals or the adsorbate. Van der Waals interactions, electrostatic interactions, hydrogen bonds, diffusion, and hydrophobic interactions could all be involved. The opposite scenario is the chemisorption mechanism which involves valence and electronic orbital forces between the absorbent and adsorbate. It produces an irreversible chemical connection to the adsorbent's surface. Complex formation, chelation, covalent bonding, redox reaction, and proton displacement can all be part of the mechanism behind the chemisorption process53,54,55. The ΔH0 value can be used to determine the physicochemical characteristics of adsorption; when it is between 0 and 20 kJ/mol, adsorption is physisorption; between 20 and 80 kJ/ mol, both physisorption and chemisorption occur; and between 80 and 400 kJ/mol, the adsorption is followed by chemisorption56,57,58. According to the calculated ΔH0 (Table 10), the adsorption type for HMNP is physical–chemical adsorption. Due to the positively charged surface of HMNP in low-pH solutions, AR18 removal increases. The opposing charges on the molecules of AR18 and AR18 bring about electrostatic attraction between HMNP and dye. However, the outcome indicates that the AR18 and HMNP have no attraction for one other at high pH. As a result, at high pH, the elimination of AR18 molecules is reduced. The findings thus imply that chemisorption may be the mechanism of AR18 elimination in a low-pH solution. The elimination process may involve physisorption at high pH levels. Alternatively, surfactants can be utilized to improve the adsorption capacity of mineral adsorbents. HDTMA is one of the most often utilized surfactants for modification. The interaction of mineral absorbents with the hydrophobic tails of HDTMA ions, which replaces the Na+ cation on the surface of the absorbent and causes the adsorbent’s surfaces to be positively charged, causes the increase in adsorption capabilities. Because of the electrostatic interaction between the adsorbate and the surfactant-modified adsorbent, anionic dyes could be adsorbed59,60.

For economic reasons, the reusability of the chosen adsorbent plays an important role in studies. By tracking the adsorption capacity of the adsorbent for five cycles under ideal conditions, the reusability of HMNP was examined. Desorption was carried out by eluting the AR18 adsorbed on HMNP with a 0.5 M NaOH solution following each run of adsorption. The modified pumices’ good recyclability for AR18 adsorption is demonstrated in Fig. 12, which depicts a reduction in HMNP’s adsorption effectiveness from 99 to 85% after five consecutive recycles. The reusability test results revealed that the prepared HMNP sorbent shows no considerable loss in its efficiency even after five cycles. Some previous studies on different contaminants like Antimony and phosphate prove this 61,62.

Reusability of HMNP for ten successive cycles (condition: pH = 4.5, sorbent dosage = 2.375 g/l, AR18 concentration = 25 mg/l, and contact time = 70 min).

The adsorption capacity of this study was compared with other pumice adsorbents reported by other researchers. Other studies have investigated the removal of different pollutants by pumice, and their maximum adsorption capacities (Qmax) are listed in Table 11. In most studies, the maximum adsorption capacity has occurred at acidic.

In the present study, HMNP adsorbent has been synthesized for the adsorption of dye-containing industrial wastewater. CCD did prediction and optimization of the AR18 removal process with RSM. From obtained ANOVA results, it was understood that the AR18 initial concentration has the highest effect on the adsorption process while contact time has the lowest. The maximum adsorption capacity of HMNP was 12.84 mg/g with C0 = 25 mg/l, adsorbent dosage 2.375 g/l and pH = 4.5. The Langmuir isotherm equilibrium model was found best fitted in this study, and adsorption kinetic data showed a good agreement with the pseudo-second-order. The adsorption process is defined to be endothermic and random due to the Positive ΔHo and ΔS o values. Moreover, negative ΔG can be considered evidence for the spontaneous nature of HMNP. In comparison to other adsorbents, HMNP has a low maximum adsorption capacity. Due to its easy accessibility, abundance, non-toxicity, and eco-friendliness, HMNP can be considered a useful adsorbent for low concentrations of AR18 despite its low adsorption capability. Nonetheless, it might be able to adsorb other pollutants more effectively.

All data generated or analyzed during this study are available from the corresponding author upon reasonable request.

Dehghani, M. H., Najafpoor, A. A. & Azam, K. Using sonochemical reactor for degradation of LAS from effluent of wastewater treatment plant. Desalination 250, 82–86 (2010).

Article CAS Google Scholar

Dehghani, M. H., Azam, K., Changani, F. & Dehghani Fard, E. Assessment of medical waste management in educational hospitals of Tehran University medical sciences. J. Environ. Health Sci. Eng. 5, 131–136 (2008).

CAS Google Scholar

Dehghani, M. H. et al. Process optimization and enhancement of pesticide adsorption by porous adsorbents by regression analysis and parametric modelling. Sci. Rep. 11, 11719 (2021).

Article ADS CAS PubMed PubMed Central Google Scholar

Shabanloo, A. et al. Heterogeneous persulfate activation by nano-sized Mn3O4 to degrade furfural from wastewater. J. Mol. Liq. 298, 112088 (2020).

Article CAS Google Scholar

Dehghani, M. H. et al. Insights into endocrine-disrupting Bisphenol-A adsorption from pharmaceutical effluent by chitosan immobilized nanoscale zero-valent iron nanoparticles. J. Mol. Liq. 311, 113317 (2020).

Article CAS Google Scholar

Karimifard, S. & Alavi Moghaddam, M. R. Application of response surface methodology in physicochemical removal of dyes from wastewater: A critical review. Sci. Total Environ. 640–641, 772–797 (2018).

Article ADS PubMed Google Scholar

Hosseini Koupaie, E., Alavi Moghaddam, M. R. & Hashemi, S. H. Post-treatment of anaerobically degraded azo dye Acid Red 18 using aerobic moving bed biofilm process: Enhanced removal of aromatic amines. J. Hazard Mater. 195, 147–154 (2011).

Article CAS PubMed Google Scholar

Zhao, T., Li, P., Tai, C., She, J. & Yin, Y. Efficient decolorization of typical azo dyes using low-frequency ultrasound in presence of carbonate and hydrogen peroxide. J. Hazard Mater. 346, 42–51 (2018).

Article CAS PubMed Google Scholar

Oros, G., Forgacs, E. & Cserha, T. Removal of synthetic dyes from wastewaters: A review. J. Environ. Int. 30, 953–971 (2004).

Article Google Scholar

Koupaie, E. H., Moghaddam, M. R. A. & Hashemi, S. H. Bioresource technology evaluation of integrated anaerobic/aerobic fixed-bed sequencing batch biofilm reactor for decolorization and biodegradation of azo dye Acid Red 18: Comparison of using two types of packing media. Bioresour. Technol. 127, 415–421 (2013).

Article Google Scholar

Khomri, M. E. et al. Modification of low-cost adsorbent prepared from agricultural solid waste for the adsorption and desorption of cationic dye. Emergent Mater. 5, 1679–1688 (2022).

Article CAS Google Scholar

El Messaoudi, N. et al. Regeneration and reusability of non-conventional low-cost adsorbents to remove dyes from wastewaters in multiple consecutive adsorption–desorption cycles: A review. Biomass Convers. Biorefinery https://doi.org/10.1007/s13399-022-03604-9 (2022).

Article Google Scholar

Srivastava, P., Goyal, S. & Patnala, P. K. Ultrasonics Sonochemistry Degradation of reactive, acid and basic textile dyes in the presence of ultrasound and rare earths [Lanthanum and Praseodymium ]. Ultrason. Sonochem. 21, 1994–2009 (2014).

Article CAS PubMed Google Scholar

El Messaoudi, N. et al. Experimental study and theoretical statistical modeling of acid blue 25 remediation using activated carbon from Citrus sinensis leaf. Fluid Phase Equilib. 563, (2022).

El Khomri, M. et al. Optimization based on response surface methodology of anionic dye desorption from two agricultural solid wastes. Chem. Africa 5, 1083–1095 (2022).

Article Google Scholar

Shokoohi, R. et al. Adsorption of acid red 18 (AR18) by activated carbon from poplar wood–a kinetic and equilibrium study. Chemistry 7, 65–72 (2010).

CAS Google Scholar

El Khomri, M. et al. Regeneration of argan nutshell and almond shell using HNO3 for their reusability to remove cationic dye from aqueous solution. Chem. Eng. Commun. 209, 1304–1315 (2022).

Article Google Scholar

Taktak, F. & Lbay, Z. Synthesis of novel poly[2-(dimethylamino) ethyl methacrylate]/Pumice stone hydrogel composite for the rapid adsorption of humic acid in aqueous solution. J. Macromol. Sci., Part A Pure Appl. Chem. 52, 307–315 (2015).

Article CAS Google Scholar

Dehghani, M. H., Faraji, M., Mohammadi, A. & Kamani, H. Optimization of fluoride adsorption onto natural and modified pumice using response surface methodology: Isotherm, kinetic and thermodynamic studies. 34, 454–462 (2017).

Yavuz, M., Gode, F., Pehlivan, E., Ozmert, S. & Sharma, Y. C. An economic removal of Cu2+ and Cr3+ on the new adsorbents: Pumice and polyacrylonitrile/pumice composite. Chem. Eng. J. 137, 453–461 (2008).

Article CAS Google Scholar

Oztürk Akbal, F., Akdemir, N. & Nur Onar, A. FT-IR spectroscopic detection of pesticide after sorption onto modified pumice. Talanta 53, 131–135 (2000).

Article PubMed Google Scholar

Onar, A. N., Balkaya, N. & Akyüz, T. Phosphate removal by adsorption. Environ. Technol. (U. K.) 17, 207–213 (1996).

Article CAS Google Scholar

Kitis, M., Kaplan, S. S., Karakaya, E., Yigit, N. O. & Civelekoglu, G. Adsorption of natural organic matter from waters by iron coated pumice. Chemosphere 66, 130–138 (2007).

Article ADS CAS PubMed Google Scholar

Sepehr, M. N., Sivasankar, V., Zarrabi, M. & Senthil Kumar, M. Surface modification of pumice enhancing its fluoride adsorption capacity: An insight into kinetic and thermodynamic studies. Chem. Eng. J. 228, 192–204 (2013).

Article CAS Google Scholar

Soleimani, H. et al. Effect of modification by five different acids on pumice stone as natural and low-cost adsorbent for removal of humic acid from aqueous solutions–application of response surface methodology. J. Mol. Liq. 290, 111181 (2019).

Article CAS Google Scholar

Rahmani, A. R. et al. A comparative study on the removal of pentachlorophenol using copper-impregnated pumice and zeolite. J. Environ. Chem. Eng. 6, 3342–3348 (2018).

Article CAS Google Scholar

Li, Z. & Bowman, R. S. Counterion effects on the sorption of cationic surfactant and chromate on natural clinoptilolite. Environ. Sci. Technol. 31, 2407–2412 (1997).

Article ADS CAS Google Scholar

Yuan, L., Shen, J., Chen, Z. & Guan, X. Role of Fe/pumice composition and structure in promoting ozonation reactions. Appl. Catal. B 180, 707–714 (2016).

Article CAS Google Scholar

Liu, K. et al. Effects of pumice-based porous material on hydration characteristics and persistent shrinkage of Ultra-High Performance Concrete (UHPC). Materials 12, (2018).

Komur, B. et al. Fabrication of naturel pumice/hydroxyapatite composite for biomedical engineering. Biomed. Eng. Online 15, 1–20 (2016).

Article Google Scholar

Safari, G. H. et al. Trends of natural and acid-engineered pumice onto phosphorus ions in aquatic environment: Adsorbent preparation, characterization, and kinetic and equilibrium modeling. Desalin. Water Treat. 54, 3031–3043 (2015).

Article CAS Google Scholar

Alver, A. & Kılıç, A. Catalytic ozonation by iron coated pumice for the degradation of natural organic matters. Catalysts 8, (2018).

Öztel, M. D., Akbal, F. & Altaş, L. Arsenite removal by adsorption onto iron oxide-coated pumice and sepiolite. Environ. Earth Sci. 73, 4461–4471 (2015).

Article ADS Google Scholar

Depci, T. et al. Chemical characterization of Patnos scoria (Aǧri, Turkey) and its usability for production of blended cement. Physicochem. Probl. Miner. Process. 48, 303–315 (2012).

ADS CAS Google Scholar

Guang-She, L., Li-Ping, L., Smith, R. L. & Inomata, H. Characterization of the dispersion process for NiFe2O4 nanocrystals in a silica matrix with infrared spectroscopy and electron paramagnetic resonance. J. Mol. Struct. 560, 87–93 (2001).

Article ADS CAS Google Scholar

Fan, Q. H. et al. Adsorption of humic acid and Eu (III) to multi-walled carbon nanotubes: EFFECT of pH, ionic strength and counterion effect. Radiochim. Acta 97, 141–148 (2009).

Article CAS Google Scholar

Najafi Chaleshtori, A. A. et al. Removal of acid red 18 (Azo-dye) from aqueous solution by adsorption onto activated charcoal prepared from almond shell. J. Environ. Sci. Manag. 20, 9–16 (2017).

Article Google Scholar

Ravulapalli, S. & Kunta, R. Effective removal of methylene blue, a hazardous dye from industrial effluents using active carbon of F. infectoria plant. Int. J. Environ. Sci. Technol. 16, 7837–7848 (2019).

Article CAS Google Scholar

Gnanasundaram, N., Loganathan, M. & Singh, A. Optimization and Performance parameters for adsorption of Cr6+ by microwave assisted carbon from Sterculia foetida shells. IOP Conf. Ser. Mater. Sci. Eng. 206, (2017).

Chueachot, R. et al. Adsorption efficiency of methylene blue from aqueous solution with amine-functionalized mesoporous silica nanospheres by co-condensation biphasic synthesis: Adsorption condition and equilibrium studie. Mater. Today Proc. 5, 14079–14085 (2018).

Article CAS Google Scholar

Ahmadi, S. & Igwegbe, C. A. Adsorptive removal of phenol and aniline by modified bentonite: Adsorption isotherm and kinetics study. Appl. Water Sci. 8, 1–8 (2018).

Article ADS Google Scholar

Derakhshan, Z., Baghapour, M. A., Ranjbar, M. & Faramarzian, M. Adsorption of methylene blue dye from aqueous solutions by modified pumice stone: kinetics and equilibrium studies. Health Scope 2, 136–144 (2013).

Article Google Scholar

Armbruster, M. H. & Austin, J. B. The adsorption of gases on plane surfaces of mica. J. Am. Chem. Soc. 60, 467–475 (1938).

Article CAS Google Scholar

Heibati, B. et al. Removal of noxious dye-Acid Orange 7 from aqueous solution using natural pumice and Fe-coated pumice stone. J. Ind. Eng. Chem. 31, 124–131 (2015).

Article CAS Google Scholar

Crini, G., Peindy, H. N., Gimbert, F. & Robert, C. Removal of C.I. Basic Green 4 (Malachite Green) from aqueous solutions by adsorption using cyclodextrin-based adsorbent: Kinetic and equilibrium studies. Sep. Purif. Technol. 53, 97–110 (2007).

Article CAS Google Scholar

Khaled, A., El Nemr, A., El-Sikaily, A. & Abdelwahab, O. Treatment of artificial textile dye effluent containing Direct Yellow 12 by orange peel carbon. Desalination 238, 210–232 (2009).

Article CAS Google Scholar

Helard, D., Indah, S., Sari, C. M. & Mariesta, H. The adsorption and regeneration of natural pumice as low-cost adsorbent for nitrate removal from water. J. Geosci., Eng,, Environ. Technol. 3, 86 (2018).

Article Google Scholar

Bayu, S. Intercomparability of isotropic and anisotropic solar radiation models for different climatic zones of India. Environ. Prog. 30, 925–932 (2011).

Google Scholar

Azari, A. et al. Experimental design, modeling and mechanism of cationic dyes biosorption on to magnetic chitosan-lutaraldehyde composite. Int. J. Biol. Macromol. 131, 633–645 (2019).

Article CAS PubMed Google Scholar

Gómez, V., Larrechi, M. S. & Callao, M. P. Kinetic and adsorption study of acid dye removal using activated carbon. Chemosphere 69, 1151–1158 (2007).

Article ADS PubMed Google Scholar

Kuczajowska-Zadrożna, M., Filipkowska, U., Jóźwiak, T. & Szymczyk, P. The use of polysaccharides for acid red 18 anionic dye removal from aqueous solutions. Prog. Chem. Appl. Chitin. Deriv. 22, 106–117 (2017).

Google Scholar

Zhang, J., Liu, F., Gao, J., Chen, Y. & Hao, X. Ordered mesoporous TiO 2/activated carbon for adsorption and photocatalysis of acid red 18 solution. BioResources 12, 9086–9102 (2017).

Article CAS Google Scholar

Asgari, G., Roshani, B. & Ghanizadeh, G. The investigation of kinetic and isotherm of fluoride adsorption onto functionalize pumice stone. J. Hazard Mater. 217–218, 123–132 (2012).

Article PubMed Google Scholar

Mourabet, M. et al. Removal of fluoride from aqueous solution by adsorption on hydroxyapatite (HAp) using response surface methodology. J. Saudi Chem. Soc. 19, 603–615 (2015).

Article Google Scholar

Márquez, C. O., García, V. J., Guaypatin, J. R., Fernández-Martínez, F. & Ríos, A. C. Cationic and anionic dye adsorption on a natural clayey composite. Appl. Sci. (Switzerland) 11, (2021).

Xu, J. et al. Dechlorination mechanism of 2,4-dichlorophenol by magnetic MWCNTs supported Pd/Fe nanohybrids: rapid adsorption, gradual dechlorination, and desorption of phenol. ACS Appl. Mater. Interfaces 8, 7333–7342 (2016).

Article CAS PubMed Google Scholar

Zhu, D. et al. Simultaneous removal of multiple heavy metals from wastewater by novel plateau laterite ceramic in batch and fixed-bed studies. J. Environ. Chem. Eng. 9, (2021).

Wang, T. et al. Enhanced ammonium removal on biochar from a new forestry waste by ultrasonic activation: Characteristics, mechanisms and evaluation. Sci. Total Environ. 778, (2021).

Bushra, R., Mohamad, S., Alias, Y., Jin, Y. & Ahmad, M. Current approaches and methodologies to explore the perceptive adsorption mechanism of dyes on low-cost agricultural waste: A review. Microporous Mesoporous Mater. vol. 319 Preprint at https://doi.org/10.1016/j.micromeso.2021.111040 (2021).

Tan, K. B. et al. Adsorption of dyes by nanomaterials: Recent developments and adsorption mechanisms. Sep. Purif Technol., vol. 150 229–242 Preprint at https://doi.org/10.1016/j.seppur.2015.07.009 (2015).

Sari, A., Tuzen, M. & Kocal, İ. Application of chitosan-modified pumice for antimony adsorption from aqueous solution. Environ. Prog. Sustain. Energy 36, 1587–1596 (2017).

Article CAS Google Scholar

Fetene, Y. & Addis, T. Adsorptive removal of phosphate from wastewater using Ethiopian rift pumice: batch experiment. Air, Soil and Water Res. 13, (2020).

Yousefi, M. et al. Modification of pumice with HCl and NaOH enhancing its fluoride adsorption capacity: Kinetic and isotherm studies. Hum. Ecol. Risk Assess. 25, 1508–1520 (2019).

Article CAS Google Scholar

Öztürk, D. & Şahan, T. Design and optimization of Cu(II) adsorption conditions from aqueous solutions by low-cost adsorbent pumice with response surface methodology. Pol. J. Environ. Stud. 24, 1749–1756 (2015).

Article Google Scholar

Kasraee, M. et al. Adsorptive removal of humic substances using cationic surfactant-modified nano pumice from water environment: Optimization, isotherm, kinetic and thermodynamic studies. Chemosphere 307, (2022).

Download references

This research has been supported by the Tehran University of Medical Science.

Department of Environmental Health Engineering, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran

Mahboobeh Kasraee, Mohammad Hadi Dehghani & Farshad Hamidi

Center for Solid Waste Research, Institute for Environmental Research, Tehran University of Medical Sciences, Tehran, Iran

Mohammad Hadi Dehghani

Petroleum and Chemical Engineering, Faculty of Engineering, Universiti Teknologi Brunei, Bandar Seri Begawan, BE1410, Brunei Darussalam

Nabisab Mujawar Mubarak & Rama Rao Karri

Department of Biosciences, Saveetha School of Engineering, Saveetha Institute of Medical and Technical Sciences, Chennai, India

Nabisab Mujawar Mubarak

Chemical Engineering Section, Sohar University, Sohar, Oman

Natarajan Rajamohan

Department of Chemical Engineering, Dawood University of Engineering and Technology, Karachi, 74800, Pakistan

Nadeem Hussain Solangi

You can also search for this author in PubMed Google Scholar

Supervision, Conceptualization, Methodology: M.H.D., M.K. Software, Visualization, Investigation: M.H.D., F.H., R.R.K., R.N., N.H.S. Writing—review & editing: M.H.D., N.M.M.

Correspondence to Mohammad Hadi Dehghani.

The authors declare no competing interests.

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

Kasraee, M., Dehghani, M.H., Hamidi, F. et al. Adsorptive removal of acid red 18 dye from aqueous solution using hexadecyl-trimethyl ammonium chloride modified nano-pumice. Sci Rep 13, 13833 (2023). https://doi.org/10.1038/s41598-023-41100-w

Download citation

Received: 17 June 2023

Accepted: 22 August 2023

Published: 24 August 2023

DOI: https://doi.org/10.1038/s41598-023-41100-w

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.