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. 2020 Dec 23;6(1):845–856. doi: 10.1021/acsomega.0c05430

Instantaneous Adsorption of Synthetic Dyes from an Aqueous Environment Using Kaolinite Nanotubes: Equilibrium and Thermodynamic Studies

Mostafa R Abukhadra †,‡,*, Merna Mostafa †,‡, Ahmed M El-Sherbeeny §,*, Mohammed A El-Meligy ∥, Ahmed Nadeem ⊥
PMCID: PMC7808155  PMID: 33458535

Abstract

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Innovative kaolinite nanotubes (KNTs) are synthesized utilizing a simple technique involving a sonication-induced exfoliation process, followed by chemical scrolling reactions. The KNTs as a material have high reactivity and promising surface area to be used in the purification of water from cationic dyes (safranin (SF) and malachite green (MG)) and anionic dyes (methyl orange (MO) and Congo red (CR)). The kinetic studies of the four dyes SF, MG, CR, and MO show an equilibration time interval of 240 min. The SF, MG, CR, and MO dyes’ uptake reactions are in agreement with the kinetic behavior of the pseudo-first-order model and the equilibrium properties of the Langmuir model. Such modeling results, in addition to the Gaussian energies from the Dubinin–Radushkevich (D–R) model (SF (1.01 kJ/mol), MG (1.08 kJ/mol), CR (1.11 kJ/mol), and MO (1.65 kJ/mol)), hypothesize monolayer adsorption of the four dyes by physical reactions. The KNTs show theoretical qmax values of 431.6, 489.9, 626.2, and 675.5 (mg/g) for SF, MG, CR, and MO, respectively. The thermodynamic examination of SF, MG, CR, and MO adsorption reactions using KNTs verifies their adsorption by exothermic and spontaneous reactions. The KNT adsorbents achieve promising adsorption results in the presence of different coexisting ions and show significant recyclability properties. Therefore, the production of KNTs from kaolinite shows a strong effect on inducing the textural, physicochemical, and adsorption properties of clay layers as well as their affinity for different species of synthetic dyes.

1. Introduction

Extensive monitoring of various species of toxic inorganic, organic, suspended, and biological water pollutants is highly important for the safety of our contemporaneous world as they have direct negative and poisonous effects on freshwater resources, aquatic organisms, and plants.1−3 Synthetic dyes are identified as one of the extensively detected organic contaminants in different water supplies. About 90% of the known synthetic dyes are classified as toxic and hazardous compounds that can cause eutrophication, perturbation of the aquatic ecosystem, and esthetic pollution in addition to their threats to human health.4−6 Safranin (SF), malachite green (MG), methyl orange (MO), and Congo red (CR) dyes are very common types of dyes that are extensively used in several industrial and human activities.7−9

Safranin (SF) is a synthetic dye that is of basic type, and its existence in water supplies is recognized as the main reason for some negative health impacts such as respiratory tract irritation and skin irritation in addition to its role in causing injury to the conjunctiva as well as the cornea of the human eyes.10,11 Also, malachite green (MG) is a common type of highly toxic synthetic dye that is used extensively in aquaculture, medical, and food industries.4,12 Chromosomal fractures, mutagenesis, carcinogenesis, respiratory toxicity, and teratogenicity are the commonly detected health side effects of malachite green as water pollutants.13,14 Such hazardous impacts have also been reported for the acidic Congo red (CR) dye, which is a highly soluble synthetic dye and is applied widely in cosmetic, plastic, and textile industries.15,16 The presence of the Congo red dye in drinking water leads to significant toxic, carcinogenic, and mutagenic effects.2,16,17 Methyl orange (MO) is another type of acidic synthetic dye that has a vital role in the textile as well as the printing industries.5,18,19 The release of the MO dye at high concentrations has several dangerous effects as it is a toxic compound with carcinogenic and mutagenic properties.19,20

Development of promising decontamination techniques for such organic pollutants utilizing natural minerals and rocks was recommended as they are economic and easily available.21 Also, there have been continuous scientific efforts from the environmental authorities and innovative researchers to produce novel forms of adsorbents that achieved promising capacities within small time intervals.22 One-dimensional nanostructures like nanorods and nanotubes as well as clay-based nanomaterials were studied widely for the adsorption of different species of water contaminants because of their high surface area and high dispersion properties.23,24

Recently, synthetic kaolinite nanoscrolls or nanotubes (KNTs) were developed from natural kaolinite minerals and investigated as novel adsorbents for metal ions.25 Kaolinite is a clay mineral with a 1:1 sheet structure and a hydrated aluminum silicate chemical structure.14,26 It was reported that the chemical and morphological modifications of the kaolinite sheets have a strong influence on enhancing the surface reactivity, the adsorption capacity, and the surface area of kaolinite.15,28 The scrolling process of the well-developed kaolinite layered units into different types of nanotubes was observed as one of the best structural and morphological modification techniques, which results in a semicrystalline product having promising physicochemical properties and a porous structure.28 Therefore, the production of nanoscrolls or nanotubes from the kaolinite mineral will result in a promising adsorbent material with amazing adsorption properties, low production cost, simple preparation steps, and abundant natural resources for its precursor.

Unfortunately, there are no previous research studies that investigated the adsorption affinities and capacities of the KNT structure for organic pollutants, especially synthetic dyes, as well as the predicted adsorption mechanism. Therefore, this study aims to investigate the adsorption properties of synthetic kaolinite nanotubes (KNTs) as an effective and new adsorbent for different types of basic synthetic dyes (safranin dye and malachite green dye) and acidic synthetic dyes (methyl orange and Congo red dyes) and a potential product for large-scale applications. The study involves evaluation of the adsorption properties of KNTs considering the main variables of pH, contact time, dye concentrations, dosage, coexisting ions, and temperature. Additionally, the addressed dye adsorption systems are explained based on the scientific significance of their thermodynamic, equilibrium, and kinetic properties.

2. Results and Discussion

2.1. Characterization of KNTs

The formation of KNTs was confirmed by both scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM) images (Figure 1). The pseudohexagonal flakes of the kaolinite mineral (Figure 1A) were converted strongly into scrolled or folded particles of tubular forms (Figure 1B). The deep investigation of the scrolled particles in the HRTEM images reflected their formation as nanotubes of cylindrical hollow forms with an internal diameter from 2 up to 20 nm (Figure 1C,D) as compared to the pure flaky nature of kaolinite (Figure S1). The length of produced KNTs ranged from nearly 50 to about 600 nm, and the outer diameters of these tubes were detected within a range from 10 up to 50 nm.

Figure 1.

Figure 1

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SEM images of the kaolinite mineral (A) and KNTs (B) and HRTEM images of the produced KNTs (C, D).

As we presented in our previous studies, the used kaolinite mineral was identified by its diffraction peaks at 12.33° (001), 20.8° (1̅10), 24.87° (002), and 26.6° (111) that were related to its triclinic crystal system (Figure 2A.A). Dimethyl sulfoxide (DMSO)-intercalated kaolinite layers showed a reduction for most of the kaolinite peaks except the main peaks ((001) and (002)) that were observed as broad and deviated peaks (Figure 2A.B). The same two peaks were observed for methoxy kaolinite but with lower intensities than the observed peaks for DMSO/kaolinite (Figure 2A.C). After the complete formation of KNTs, the obtained pattern displays only one peak at nearly 10.6° that signifies the (001) plane of kaolinite scrolls (Figure 2A.D).25

Figure 2.

Figure 2

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XRD patterns of the kaolinite mineral, DMSO/kaolinite, methoxy kaolinite, and KNTs (A) and the Fourier transform infrared (FT-IR) spectra of the kaolinite mineral and KNTs (B).

Comparing the FT-IR spectrum of kaolinite with the one obtained for KNTs reflected no obvious changes in the chemical composition (Figure 2B). The spectrum of the kaolinite mineral demonstrated the existence of Si–O, Si–O–Al groups, Si–O–Si, OH bending, Al–OH, and Si–OH groups considering their identification bands at 456, 680, 1020, 1641, 912, 3500.2, and 3689.4 cm–1, respectively (Figure 2B.A).15 The same bands were observed for KNTs but at shifted positions, which suggested distortion of the basic kaolinite units during the conversion processes (Figure 2B.B). Also, the expected binding of the intercalated organic compounds with the siloxane groups or the basal oxygen has substantial impact on the structural units of KNTs.28

As for the texture of KNTs, the change of the isotherm curve from type II for the kaolinite mineral to type IV with an H3 hysteresis loop for KNTs reflected changes in the morphology from macroporous plates to nanoporous materials in which the pores were of tubular or cylindrical forms25 (Figure S2). Therefore, the surface area increased from 10 m2/g for the kaolinite mineral to 105 m2/g for KNTs. Moreover, the total porosity increased significantly from 0.052 cm3/g for the kaolinite mineral to 0.51 cm3/g for KNTs. The average pore diameter of the produced KNTs was 12 nm, and hence they could be regarded as having a mesoporous structure. Also, the transformation of the flaky sheets of kaolinite into nanotubes had a slight effect on the ion-exchange properties. The ion-exchange capacity slightly increased from 3 mequiv/100 g to 5.2 mequiv/100 g after the production of KNTs. This is in agreement with the expected distortion in both the silicon tetrahedrons and the aluminum octahedrons of kaolinite.

2.2. Influence of Process Variables on Adsorption

2.2.1. Influence of pH on Adsorption

The pH value of the polluted water has a controlling effect on the ionization states of the dye molecules as well as the surficial charges of the solid adsorbents.29 The experiments considering the influence of pH as the essential variable were carried out for a wide range from highly acidic pH 2 to alkaline pH 10. Moreover, the other studied variables were considered at selected experimental values of 500 mL as the treated volume, 120 min as the tested contact time, 0.2 g/L as the KNT solid dosage, adjusted 100 mg/L as the tested concentration of the four dyes, and 25 °C as the operating temperature. However, the affinity of KNTs for SF and MG dyes significantly increased on performing the tests under alkaline conditions, and their uptake capacity for CR and MO dyes declined strongly under such basic environments (Figure 3). These different adsorption trends are related to the ionization properties of the dyes as the SF and MG dyes are of cationic type, while the CR and MO dyes are of anionic type. Therefore, the deprotonated sites of KNTs that are negatively charged receptors at such basic environments have highly attractive properties for cationic SF and MG dyes (positively charged molecules) and strong repulsive properties for anionic CR and MO dyes (negatively charged molecules).30 Moreover, the reported dipolar properties of CR as cationic molecules under acidic environments (pH < 5.5) and as anionic molecules at pH values higher than 5.5 greatly affected the adsorption behaviors of CR molecules.31 The greatest uptake capacities for SF (152.4 mg/g) and MG (173 mg/g) were achieved at pH 10. On the other hand, the highest uptake capacities of CR (184.3 mg/g) and MO (206.2 mg/g) dyes were observed at pH 2 (Figure 3). The previously mentioned results and the related explanation were supported by the detected pH value of zero point charge (pH(zpc)) considering the measured ζ potential values. The measured pH(zpc) value of KNTs is 6.73, and this value is close to that obtained for raw kaolinite (pH 6.54). The value of the pH(zpc) reflected the enrichment of the KNT surface with the negative charges during the adsorption of the four dyes at pH values higher than these values. This value is close to the obtained value for kaolinite (pH 6.54).

Figure 3.

Figure 3

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Effect of solution pH values on the uptake capacities of KNTs for SF, MG, CR, and MO dyes.

2.2.2. Influence of Contact Time on Adsorption

The uptake behaviors for SF, MG, CR, and MO dyes by KNTs were followed from 30 up to 600 min. The other inspected variables were considered at selected experimental values of 500 mL as the treated volume, 0.2 g/L as the KNT solid dosage, 100 mg/L as the tested concentration of the four dyes, and 25 °C as the operating temperature. The adsorption pH values were selected to be 10 for SF and MG cationic dyes and 2 for CR and MO anionic dyes.

The observed SF, MG, CR, and MO adsorption curves are of segmental shapes and different slopes, which suggested strong variations in the dye uptake rates (Figure 4). The observed segments during the initial stages of the curves for both the cationic and anionic dyes are of steep slopes (Figure 4). This proves an immediate increase in the adsorbed dye molecules with the initiation of the KNT-based adsorption reactions. This is followed by noticeable segments of small slopes or nearly plateau forms, signifying limited or nearly fixed variations in the dye adsorption rates. These segments are commonly identified as the saturation or the equilibration segments (Figure 4). The reported decrease in the KNT uptake rates for the dyes on increasing the studied contact time depends on the availability of the effective uptake sites.30 The receptor sites of KNTs were highly available during the initiation of the reaction, which caused abrupt capturing of the dye molecules. After a certain time, the receptors became mostly occupied by the dye molecules, making the KNTs’ capacity restricted to the remaining sites on the surface of KNTs.22 The equilibrium time was identified as 240 min for SF, MG, CR, and MO dyes with equilibration capacities of 197, 209, 243.4, and 283 mg/g, respectively (Figure 4).

Figure 4.

Figure 4

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Uptake behaviors of SF, MG, CR, and MO dyes as a function of the contact time using KNTs.

2.2.3. Influence of Dye Concentrations on Adsorption

Evaluation of the behavior of KNTs during the uptake of different concentrations of SF, MG, CR, and MO dyes (50–400 mg/L) is essential to determine its maximum capacity and its equilibrium properties.32 The other studied variables were considered at selected experimental values of 500 mL as the treated volume, 0.2 g/L as the KNT solid dosage, 480 min as the reported equilibrium time, and 25 °C as the operating temperature. The adsorption pH was selected to be 10 for SF and MG cationic dyes and 2 for CR and MO anionic dyes. The quantities of the adsorbed anionic as well as cationic dyes by KNTs increased strongly on testing high concentrations of the four dyes (Figure S3). The intensification of the driving forces of the dye molecules at the highest concentrations supports the extensive interactions between their ions and the effective receptors of KNTs.28,33 This can be detected for SF, MG, CR, and MO until tested concentrations of 300, 250, 300, and 200 mg/L, respectively, which are the equilibrium concentrations of the studied systems (Figure S3). Such concentrations resulted in complete or partial saturation of the sites of KNTs by the dye molecules, at which the material could attain its maximum capacity. The experimentally detected maximum capacities for SF, MG, CR, and MO dyes are 427.6, 464.4, 586.5, and 639.2 mg/g, respectively (Figure S3).

2.2.4. Influence of KNT Dosages on Adsorption

The predicted influence of KNT quantities on the removal of SF, MG, CR, and MO dyes was studied experimentally from about 0.2 to 1 g/L. The other studied variables were considered at selected experimental values of 500 mL as the treated volume, 480 min as the reported equilibrium time, 100 mg/L as the tested concentration of the four dyes, and 25 °C as the operating temperature. The adsorption pH was selected to be 10 for SF and MG cationic dyes and 2 for CR and MO anionic dyes. Figure 5 verifies significant and positive effects of KNT dosage on increasing the removal efficiency of SF, MG, CR, and MO dyes. This was explained to be associated with the enrichment of the dye solutions in the active sites of KNTs.4 The adsorption percentage of the SF dye was enhanced from 39.5 up to 100% with the increase of the KNT dosage from 0.2 up to 1 g/L. For the MG cationic dye, the attained percentage using 0.2 g/L KNTs (41.8%) was augmented to 100% after using 1 g/L (Figure 5). Also, the removal of CR and MO anionic dyes significantly increased by the used KNT dosage as the examined concentrations (100 mg/L) were totally removed using about 0.8 g/L KNTs (Figure 5).

Figure 5.

Figure 5

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Removal percentages of SF, MG, CR, and MO dyes using different dosages of KNTs.

2.3. Kinetic and Equilibrium Studies

2.3.1. Kinetic Modeling

The kinetic study of SF, MG, CR, and MO uptake reactions by KNTs was accomplished by the mathematical fitting process of the experimental results with the formula of the intraparticle-diffusion model. Additionally, the pseudo-first-order, the pseudo-second-order, and the Elovich models were adopted in this study. The descriptive equations of these models, which were used in the fitting of SF, MG, CR, and MO data, are listed in Table S1. The SF, MG, CR, and MO intraparticle-diffusion curves have three obvious segments without intersection with the source points (Figure 6A). These segments verified the existence of different types of dye adsorption mechanisms that were not restricted only to the diffusion reaction of the dye molecules toward the receptors of KNTs.21 The first segment was the dominant one in the four curves and hypothesized uptake of SF, MG, CR, and MO dyes essentially by the exterior receptors of KNTs27 (Figure 6A). This showed the uptake of most of the dissolved dye molecules (SF, MG, CR, and MO) by this mechanism.

Figure 6.

Figure 6

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Fitting of the dye adsorption data with (I) intraparticle diffusion model, (B) pseudo-first-order kinetic model, (C) pseudo-second-order kinetic model, (D) Langmuir isotherm model, (E) Freundlich isotherm model, and (F) Dubinin–Radushkevich isotherm model.

This was followed by another segment that covered a significant period during the uptake of SF, MG, CR, and MO dyes (Figure 6A). This segment emphasized diminution of the external adsorption mechanism as all of the external receptors of KNTs were consumed by the molecules of the four dyes. Additionally, this segment verified the dominance of the layered adsorption processes as the essential mechanism and their considerable role during the uptake of SF, MG, CR, and MO dyes by KNTs at the intermediate stages of the reactions.25,34 By the end of this segment, another new segment was detected in the curves of SF, MG, CR, and MO dyes that appeared to be of negligible effect (Figure 6A). This segment was detected basically after the saturation of all of the external and internal receptors of KNTs by the dye molecules. The observation of this segment establishes the uptake of SF, MG, CR, and MO as thick coating layers for the KNT fractions and might be formed by inter-ionic attraction or by different types of molecular association processes.34

The χ2 values as well as the values of correlation coefficient (R2) were used to study the fitting degree of adsorption data of SF, MG, CR, and MO dyes with the other three kinetic models (Figure 6B,C). Although two models (pseudo-first- and pseudo-second-order models (Figure 6B,C)) had high correlation coefficients for the four dyes, the χ2 values suggested better agreement with the first-order supposition than the second-order supposition (Table 1). Such fitting results declared the adsorption of the dyes by physical processes which will be supported by further equilibrium studies.35 The estimated values of the experimental SF (197 mg/g), MG (209 mg/g), CR (243.4 mg/g), and MO (283 mg/g) uptake capacities (qe) close to the theoretical values from the pseud-first-order model (202 mg/g (SF), 217 mg/g (MG), 251.7 mg/g (CR), and 294.3 mg/g (MO)) support the fitting results (Table 1).

Table 1. Theoretical Parameters for the Investigated Kinetic and Equilibrium models.
kinetic models
model parameters SF MG CR MO
pseudo-first-order K1 (min–1) 4.9 × 10–7 7.47 × 10–5 2.72 × 10–6 4.49 × 10–6
qe(Cal) (mg/g) 202 217 251.7 294.3
R2 0.98 0.98 0.99 0.99
χ2 2.12 1.86 1.12 0.87
pseudo-second-order k2 (g/(mg min)) 2.49 1.95 2.26 2.09
qe(Cal) (mg/g) 207 221.4 254.2 297
R2 0.98 0.98 0.98 0.98
χ2 2.7 2.54 1.45 1.22
Elovich β (g/mg) 0.013 0.014 0.011 0.01
α (mg/(g min)) 3.23 4.49 4.2 4.72
R2 0.88 0.86 0.89 0.91
χ2 5.8 6.6 5.3 4.2
isotherm models
model parameters SF MG CR MO
Langmuir qmax (mg/g) 431.6 489.9 626.2 675.5
b (L/mg) 3.7 × 10–6 4.07 × 10–5 1.02 × 10–4 9.3 × 10–4
R2 0.99 0.98 0.98 0.90
χ2 0.87 2.14 2.23 3.6
RL 0.99–0.998 0.98–0.997 0.96–0.99 0.73–0.95
Freundlich 1/n 0.45 0.57 0.63 0.71
kF (mg/g) 182 234.5 128.8 30.7
R2 0.99 0.97 0.97 0.87
χ2 2.3 4.7 4.36 5.7
D–R model β (mol2/kJ2) 0.496 0.43 0.403 0.183
qm (mg/g) 446 486.9 607.4 667.8
R2 0.99 0.96 0.95 0.84
χ2 4.6 6.23 6.8 7.3
E (kJ/mol) 1.01 1.08 1.11 1.65
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The significant fitness of the adsorption data of the four dyes with the second-order supposition demonstrated the existence of some supporting mechanisms that have more chemical characteristics such as the surface complexation reactions, electron sharing reactions, and electron exchange reactions.36 This was confirmed by the considerable agreement between the dye adsorption data and the Elovich kinetic model, which also reflected the energetic heterogeneous surface of KNTs during the uptake of SF, MG, CR, and MO dyes37 (Figure S4).

2.3.2. Isotherm Modeling

The equilibrium behaviors of SF, MG, CR, and MO adsorption reactions using KNT adsorbents were followed considering the extent of agreement with the hypothesis of the theoretical Langmuir and Freundlich models in addition to the Dubinin–Radushkevich (D–R) model (Table S1). The correlation coefficients (R2), as well as the χ2 parameters of the fitting processes, are presented in Table 1. The uptake of the cationic dyes (SF and MG) and the anionic dyes (CR and MO) followed the presumption of the Langmuir (Figure 6D) rather than the Freundlich model (Figure 6E). This hypothesized the existence of the adsorbed SF, MG, CR, and MO dyes in monolayer forms and verified their uptake by different types of homogeneous active sites on the reactive surface of KNTs.25 Moreover, the adsorption of SF, MG, CR, and MO dyes occurred by favorable reactions as estimated from their RL parameters (Table 1). The predicted qmax values of SF, MG, CR, and MO dyes were calculated from the Langmuir fitting process and were 431.6, 489.9, 626.2, and 675.5 mg/g, respectively.

The assessment of the D–R isotherm model was performed using values of its theoretical parameters for understanding the nature of SF, MG, CR, and MO adsorption reactions as well as their maximum adsorption capacities (Figure 6F). The Gaussian energies (SF-1.01, MG-1.08, CR-1.11, and MO-1.65 (kJ/mol)) were calculated from the excellent fitting with the D–R model, and the reported values were related essentially to physical adsorption reactions (less than 8 kJ/mol)21 (Figure 6F and Table 1). Additionally, the expected qmax values of SF, MG, CR, and MO as fitting parameters for the model were 446, 486.9, 607.4, and 667.8 mg/g, respectively.

2.4. Thermodynamics

The thermodynamics of SF, MG, CR, and MO adsorption reactions using the prepared KNT adsorbent were followed within an experimentally studied temperature range from 25 °C as the starting value to 45 °C as the upper value. The other studied variables were considered at selected experimental values of 500 mL as the treated volume, 0.2 g/L as the KNT solid dosage, 100 mg/L as the tested concentration of the four dyes, and 480 min as the contact time. The adsorption pH was selected to be 10 for SF and MG cationic dyes and 2 for CR and MO anionic dyes. The essential descriptive parameters of the thermodynamic properties (ΔH° (enthalpy), ΔS° (entropy), and ΔG° (Gibbs free energy)) are presented in Table 2. Both ΔH° and ΔS° values were determined based on the commonly used linear fitting process between the experimental data and van’t Hoff equation (eq 1) (Figure S5). The value of the incorporated Langmuir constant (Kc) in eq 1 was determined from eq 2 where the Kd constant is the ratio of the dye uptake capacities to their equilibrium concentrations.38 The ΔG° values as theoretical parameters were calculated from eq 3 directly.25

2.4. 1
2.4. 2
2.4. 3

The negative signs that were reported for the enthalpy values of the cationic dyes (SF (−16.15 kJ/mol) and MG (−12.73 kJ/mol)) as well as the anionic dyes (CR (−7.45 kJ/mol) and MO (−10.09 kJ/mol)) verified their exothermic adsorption by KNTs (Table 2). Moreover, the calculated entropy values with a negative sign for the SF dye and with positive signs for MG, CR, and MO dyes verified changes in randomness properties at the interface between KNTs and the tested dyes (Table 2). While the randomness properties of SF uptake reaction decreased with the temperature, the randomness of MG, CR, and MO uptake reactions increased observably with the temperature (Table 2).21 The calculated free energies of SF, MG, CR, and MO adsorption reactions were negative values at all of the studied temperatures (Table 2). These negative values revealed spontaneous, feasible, and favorable dye uptake reactions in the presence of KNTs as the adsorbent.21 The entropy and free energy values for the SF, MG, CR, and MO adsorption reactions were within the suggested range for the physisorption reactions, which strongly matched the results of the previously investigated kinetic and isotherm models.29

Table 2. Thermodynamic Parameters for the Uptake of SF, MG, CR, and MO Dyes by KNTs.

parameters temperature SF MG CR MO
ΔGo (kJ/mol) 298.15 –12.88 –13.12 –13.81 –14.60
303.15 –12.95 –13.19 –13.92 –14.65
308.15 –12.95 –13.25 –14.00 –14.67
313.15 –12.88 –13.23 –14.12 –14.75
318.15 –12.73 –13.18 –14.23 –14.87
323.15 –12.64 –13.19 –14.36 –14.99
ΔH° (kJ/mol) –16.15 –12.73 –7.45 –10.09  
ΔS° (J/(K mol)) –10.67 1.48 21.33 14.99  
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2.5. Recyclability

The suitability of KNTs to be recycled several times for the adsorption of the cationic and anionic dyes was assessed for five runs as a vital factor deciding the commercial value of the product. The regeneration of the KNT particles involved washing of KNTs with NaOH aqueous solution (0.2 M) at an adjusted temperature of 50 °C under continuous shaking for 3 h using an orbital shaker in a hot water bath for the samples that were used in the uptake of anionic dyes. The samples that were applied in the adsorption of cationic dyes were washed with dilute HCl acid (10%) for 60 min. Then, the solid KNT particles were isolated and washed again extensively using distilled water, and this was repeated for three cycles and each cycle was for 10 min. Finally, the washed KNT fractions were dried at 85 °C for 12 h and used in the next recyclability cycle. The accomplished adsorption recyclability experiments were conducted at the pre-identified best uptake conditions (500 mL as the treated volume, 480 min as the reported equilibrium time, 100 mg/L as the tested concentration of the four dyes, 1 g/L as the incorporated KNT solid dosage, and 25 °C as the operating temperature). The adsorption pH was selected to be 10 for SF and MG cationic dyes and 2 for CR and MO anionic dyes.

The obtained data for the KNT recyclability tests proved the high efficiency of KNTs in the adsorption of the four dyes for the addressed five runs considering the studied concentration (100 mg/L) (Figure S6). The KNTs as the adsorbent showed removal percentages for the SF dye higher than 97.5% for three recyclability cycles, higher than 94.4% for four recyclability cycles, and higher than 91% for the addressed five recyclability cycles (Figure S6). Also, MG removal percentages higher than 99% for two cycles, higher than 98.3% for four cycles, and higher than 93.5% for five cycles were obtained (Figure S6). For the CR dye, the recyclability studies emphasized removal percentages higher than 98.6% for three cycles and higher than 95% for five cycles (Figure S6). For the MO dye, removal percentages higher than 99% for three cycles, higher than 98.4% for four cycles, and higher than 96.5% for all of the studied five cycles were documented (Figure S6). The efficiency of KNTs for the adsorption of SF, MG, CR, and MO dyes showed a decrease with increasing number of recyclability tests. The continuous occupation of the main receptors by the dyes molecules and the expected binding between the siloxane groups and the dyes molecules caused a reduction in the availability of such sites and in turn the efficiency of KNTs.

2.6. Influence of Coexisting Ions

The role of coexisting anions together with their activity as competitive ions for SF, MG, CR, and MO dye molecules during their uptake by KNTs was studied using four types of commonly detected water pollutants (PO43–, NH4+, Pb2+, and Zn2+). The performed experiments were assessed at the pre-identified best uptake conditions (500 mL as the treated volume, 480 min as the reported equilibrium time, 100 mg/L as the tested concentration of the four dyes, 1 g/L as the incorporated KNT solid dosage, and 25 °C as the operating temperature).

For the SF dye, the adsorption percentages dropped to 78.3, 86.4, 42.6, and 44.7% in the presence of PO43–, NH4+, Pb2+, and Zn2+ as coexisting ions, respectively (Figure 7). For the MG dye, the incorporation of PO43–, NH4+, Pb2+, and Zn2+ as competitive ions reduced the adsorption percentages to 82.6, 89.4, 47.2, and 53.6%, respectively (Figure 7). For the CR dye, its removal efficiency was also affected significantly by the existence of the selected competitive ions. The CR removal values reduced to 61.7, 90.4, 57, and 51.2% by the coexistence of PO43–, NH4+, Zn2+, and Pb2+, respectively (Figure 7). Even for the removal of the anionic MO dye, the values reduced to 83.5, 92.6, 70.3, and 65.6% for the same coexisting ions of PO43–, NH4+, Zn2+, and Pb2+, respectively (Figure 7). Generally, the presented results reflected a strong negative effect of the heavy metal ions on the affinity of KNTs for the SF and Mg dyes. Also, the chemical ions of phosphate and ammonium show considerable effect on the adsorption of these basic dyes. For the anionic dyes (CR and MO), the studied coexisting ions have significant impact on the affinity of KNTs for their molecules, but KNTs show a higher affinity for them in the presence of all of the studied competitive ions. The decrease in the affinity of KNTs for the dyes in the presence of coexisting ions was previously related to their competitive effect with dye molecules on the free active sites in addition to the predicted compensation of the solid charge by the ions.39 Based on previously reported results, the KNT particles exhibit higher efficiency in the purification of water from the cationic and anionic dyes even in the presence of other species of water pollutants. This qualifies KNTs to be incorporated effectively in remediation techniques.

Figure 7.

Figure 7

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Effect of different coexisting (phosphate (PO), ammonium (NH), Pb2+ ions (Pb), and Zn2+ ions (Zn)) ions on the uptake of SF (A), MG (B), CR (C), and MO (D) dyes using KNTs.

2.7. Adsorption Mechanism

KNTs as a modified clay nanostructure are a highly active scrolled tetrahedron and octahedron sheets of kaolinite mineral. Such scrolled layered units are characterized by highly exposed and dominant siloxane groups (Al–OH and Si–OH).40 The siloxane groups were reported as very active groups that have strong reactivity to form a complex with different species of dissolved chemical ions in addition to their role in the capturing of such ions by different types of electrostatic interactions.40 The obtained FT-IR spectra of the incorporated KNTs for the adsorption of SF, MG, CR, and MO showed a strong reduction for the well-known bands of Al–OH and Si–OH (Figure S7). Such observations might be related to their predicted consumption during the adsorption of the four dye molecules. This emphasizes their role as essential sites during the electrostatic attraction of the charged dye molecules. The observation of several bands related to the chemical groups of the studied dyes indicated their effective role in the complexation processes during the capturing of SF, MG, CR, and MO molecules by KNTs (Figure S7). The reported groups of SF molecules are −NH (3460 cm–1) and aromatic-N groups (1334 cm–1), C=C (1603 cm–1), and C–H (1422 cm–1).41 The reported chemical groups of MG are C–H (2960 cm–1), C=C (1573.4 cm–1), and C–N (1324 cm–1).42 The identified groups of CR are −CH2 (2934 cm–1), N=N (1580 cm–1), and C–N (1410 cm–1). The identified groups of the MO dye are C–H (stretching, 2973 cm–1), C=C (vibration, 1584 cm–1), and N=N (1534 cm–1).43 Previous results verified the occurrence of a strong interaction between the siloxane groups (OH-bearing groups) and the ions of the four dyes forming new hydrogen bonds.41,44

Therefore, the adsorption mechanism of SF, MG, CR, and MO molecules by KNTs involved two essential mechanisms. The first mechanism was related to the chemical complexation of the exposed Al–OH and Si–OH groups or the basal oxygen of the structural units of KNTs and the ions of the studied dyes by different types of hydrogen bonding.45 The second mechanism was related to different types of electrostatic attraction between the charged dye ions and the charged structural units of KNTs.45 Other studies verified the effective role in the predicted intercalation of the layered units by the organic pollutants, which was supported by the presence of KNTs as multilayer scrolls of kaolinite.44

2.8. Comparison Study

The achieved SF, MG, CR, and MO uptake capacities by KNTs compared well with other highly effective adsorbents reported in the literature (Table 3). The synthetic KNTs as an adsorbent for both the cationic and anionic dyes show higher efficiency than most of the listed adsorbents in the table. The KNTs as a modified form of kaolinite appears to be more promising than several types of clay minerals such as kaolinite, bentonite, serpentinite, and halloysite either in their pure phase or their modified forms. The presented results reflected obvious enhancement in the affinity of the kaolinite layers after their scrolling process into nanotubes as compared to the normal flaky layers. This is related mainly to the increase in the reactivity and the surface area of KNTs as compared to raw kaolinite. Also, it showed higher capacities than several synthetic adsorbents including CNT-based adsorbents, LDH-based adsorbents, some biogenic adsorbents, some polymers, and some metal oxide-based adsorbents (Table 3).

Table 3. Comparison between the Adsorption Capacities of KNTs and Other Natural and Synthetic Adsorbents for SF, MG, CR, and MO Dyes.

cationic dyes
 anionic dyes
adsorbent qmax (mg/g) reference adsorbent qmax (mg/g) reference
Safranin Dye Congo Red Dye
Ppy NF/Zn–Fe LDH 63.4 (22) serpentine 93.45 (33)
glass-MCM-48 62.5 (46) phosphate/kaolinite 149.25 (14)
activated carbon 576 (47) chitosan/montmorillonite 290 (16)
MCM-41 68.8 (48) willow leaf AlOOH 420 (64)
MgO-FLG-FE 201.1 (49) Na montmorillonite 58.21 (15)
araphene oxide/chitosan 425 (50) HDTMA/clinoptilolite 200 (65)
N/porous graphite 20.66 (30) ZnO–AlOOH 524 (64)
fume-MCM-48 57.47 (46) Mg–Al LDH 584.6 (66)
clinoptilolite 42.9 (10) Ni/Co-LDH 909.2 (67)
ferruginous kaolinite 59.3 (51) CTAB–H2SO4/celery residue 526 (68)
magnetic clay 18.48 (52) hierarchical ZnO 334 (64)
raw kaolinite 14.37 this study NiO–Al2O3 357 (69)
KNTs 431.6 this study γ-Al2O3 416 (70)
Malachite Green Dye bentonite/zeolite-NaP 46.29 (71)
Pinus roxburghii cone 250 (13) NiCo2O4 366 (72)
activated carbon 395 (5) NiO 534 (73)
MBCNF/GOPA 270.27 (53) Raw kaolinite 40.6 this study
chitosan/polyacrylic acid/bentonite 454.55 (54) KNTs 626.2 this study
Artocarpus odoratissimus leaves 422 (55) Methyl Orange Dye
CMC-g-P(AAm) 158.1 (56) chitosan/bentonite 136.8 (74)
CMC-g-P(AAm)/MMT 172.4 (56) CH/poly(vinyl alcohol)/zeolite 153 (75)
nanochitosan-STP 317 (57) pHEMA-chitosan-MWCNTs 306 (76)
graphene oxide/lignin aerogels 113.5 (11) functionalized CNTs/TiO2 42.85 (77)
Fe3O4/PT/GO 560.58 (58) functionalized CNTs 310 (78)
biochar/nZVI 515.77 (59) zeolite NaA/CuO 79.42 (79)
mesoporous carbon 476.1 (60) NiFe-LDH 169 (80)
reduced graphene oxide 576.2 (61) acid-salt/CoAl LDH 827.4 (81)
activated carbon 210.1 (62) h-MoS2 41.5 (19)
carbon/Zn–Al-LDH 126.58 (63) 3D l PbS/ZnO 159 (17)
raw kaolinite 63.4 this study raw kaolinite 11.5 this study
KNTs 489.9 this study KNTs 675.5 this study
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3. Conclusions

Kaolinite nanotubes (KNTs) were produced and used in the purification of water from cationic dyes (safranin dye (SF) and malachite green dye (MG)) and anionic dyes (methyl orange dye (MO) and Congo red dye (CR)). The product exhibited theoretical qmax values of 431.6, 489.9, 626.2, and 675.5 mg/g for SF, MG, CR, and MO, respectively. The SF, MG, CR, and MO dye uptake reactions fitted excellently with the kinetic behavior of the pseudo-first-order (R2 > 0.9) model and equilibrium behavior of the Langmuir model (R2 > 0.9). The equilibrium results, the thermodynamic parameters, and the values of Gaussian energies for the four dyes (less than 8 kJ/mol) suggested monolayer adsorption by exothermic, spontaneous, and physical reactions. The product demonstrated promising adsorption results even in the presence of other coexisting ions and showed significant recyclability properties.

4. Experimental Work

4.1. Materials

The kaolinite mineral that was used in the scrolling process was obtained from CMRDI Institute, Egypt. The used chemicals are NaOH pellets (Sigma-Aldrich; 97% purity; CAS: 1310-73-2), dimethyl sulfoxide (DMSO) (Sigma-Aldrich; >99.5% purity; CAS: 67-68-5), methanol (Sigma-Aldrich; >99.9% purity; CAS: 67-56-1), and cetyltrimethylammonium bromide (CTAB) (Sigma-Aldrich; >98% purity; CAS: 57-09-0). The chemicals are of analytical grade and incorporated directly in the reactions without any purification processes. The safranin-O dye (C20H19ClN4) (≥85% dye content, Sigma-Aldrich; CAS: 477-73-6), malachite green dye (C23H25N2) (90% dye content, Sigma-Aldrich; CAS: 18015-76-4), Congo red dye (C32H22N6Na2O6S2) (34% dye content, Sigma-Aldrich; CAS: 573-58-0), and methyl orange dye (C14H14N3NaO3S) (85% dye content, Sigma-Aldrich; CAS: 547-58-0) powders were obtained from Sigma-Aldrich, Egypt, as the sources of the synthetic dye contaminants.

4.2. Synthesis Steps of KNTs

The production of KNTs was completed considering the three main steps reported by Abukhadra et al.25 This involved breaking of the hydrogen bonds, exfoliation of the kaolinite layers, and scrolling of the exfoliated layers. About 15 g of the kaolinite powder was mixed with DMSO (50 mL; 80%), and the resulting mixture was stirred for about 24 h as an essential step to confirm the destruction of the hydrogen bonds and the intercalation of the kaolinite layers with the DMSO molecules. Afterward, the resulting particles from this stage were washed five times with methanol for nearly 20 min for developing hybrid materials of methanol-intercalated kaolinite known as methoxy kaolinite. This hybrid product was treated with the surfactant solution (500 mL of CTAB (1 mol/L)), and this continued for 2 days to verify effective expansion and exfoliation of the kaolinite layers from each other. The expansion step was continued effectively using sonication waves (80%) for another 48 h, which resulted finally in scrolled layers of kaolinite in the form of nanotubes. This was followed by separation of the product from the solution, which was washed with both methanol and distilled water and dried at 65 °C for 10 h.

4.3. Characterization Techniques

The crystal structure of KNTs was identified by a PANalytical X-ray diffractometer (Empyrean). The XRD results were obtained within a selected range from 5 to 70° and a scanning speed of 5°/min at 40 kV. A scanning electron microscope (Gemini, Zeiss-Ultra 55) was employed for determining the surficial morphology. The microscopic investigation was performed after coating the material using thin gold layers and at a certain voltage of 30 kV as an accelerating voltage. A transmission electron microscope (JEOL-JEM2100) was used for studying the internal structures of KNTs at 200 kV as an acceleration voltage. A Fourier transform infrared spectrometer (Shimadzu) was used to follow the expected changes in the chemical groups of KNTs. The spectrum of the material was determined at scans of 37°, adjusted resolution of about 4 cm–1, and selected frequency from 400 cm–1 as the starting point to 4000 cm–1 as the upper limit. The porosity and the surface area of KNTs were measured based on its N2 adsorption/desorption isotherm curve that was treated by BJH and Brunauer–Emmett–Teller (BET) methods. This was conducted using a surface area analyzer after a preprocessing step that involved degassing of the material for 5 h at 300 °C under vacuum, and the estimation temperature was adjusted to be 77 K. ζ potential values of the synthetic KNTs were determined at different pH values using a zetasizer with a disposable ζ cell (Malvern, version 7.11) to detect pH(zpc).

4.4. Adsorption System

The tested samples were prepared by directly dissolving certain quantities of the dye powder in distilled water (1000 mg/L in 1000 mL). The affinity of KNTs for SF, MG, CR, and MO dyes was evaluated by batch uptake experiments considering the main variables (pH, time (min), KNT dosage (g/L), tested dye concentration (mg/L), and temperature (°C)). All of the accomplished experiments for each variable were repeated as three runs, and the determined results were presented as average values during the evaluation of the uptake behavior. The principal procedures involved a homogeneous dispersion of the KNTs at a certain dosage (0.2–1 g/L) in 500 mL of dye aqueous solutions (50–400 mg/L) for certain intervals (30–480 min). As an initial stage, the influence of pH was examined from pH 2 as the starting point to pH 10 as the upper experimental limit. By the end of the experiments, the purified samples were analyzed directly by a UV–vis spectrophotometer to measure the residuals considering λmax values of the dyes (521 nm for SF, 617 nm for MG, 497 nm for CR, and 460 nm for MO).

Acknowledgments

The authors extend their appreciation to the Deputyship for Research & Innovation, “Ministry of Education” in Saudi Arabia, for funding this research work through project number IFKSURG-1440-047.

Supporting Information Available

The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acsomega.0c05430.

  • Theoretical equations of the kinetic and isotherm models (Table S1); TEM image of kaolinite (Figure S1); N2 adsorption/desorption isotherm curve of KNTs (Figure S2); uptake capacity of KNTs at different concentrations of the dyes (Figure S3); Elovich kinetic model (Figure S4); fitting of the results with the van’t Hoff equation (Figure S5); recyclability results of KNTs (Figure S6); and FT-IR spectra of KNTs after the adsorption tests (Figure S7) (PDF)

Author Contributions

This article was written through the contributions of all authors. All authors have given approval to the final version of the manuscript

The authors declare no competing financial interest.

Supplementary Material

ao0c05430_si_001.pdf (469.9KB, pdf)

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