Effective Removal of Sulfonamides Using Recyclable MXene-Decorated Bismuth Ferrite Nanocomposites Prepared via Hydrothermal Method

Developing a simple and efficient method for removing organic micropollutants from aqueous systems is crucial. The present study describes the preparation and application, for the first time, of novel MXene-decorated bismuth ferrite nanocomposites (BiFeO3/MXene) for the removal of six sulfonamides including sulfadiazine (SDZ), sulfathiazole (STZ), sulfamerazine (SMZ), sulfamethazine (SMTZ), sulfamethoxazole (SMXZ) and sulfisoxazole (SXZ). The properties of BiFeO3/MXene are enhanced by the presence of BiFeO3 nanoparticles, which provide a large surface area to facilitate the removal of sulfonamides. More importantly, BiFeO3/MXene composites demonstrated remarkable sulfonamide adsorption capabilities compared to pristine MXene, which is due to the synergistic effect between BiFeO3 and MXene. The kinetics and isotherm models of sulfonamide adsorption on BiFeO3/MXene are consistent with a pseudo-second-order kinetics and Langmuir model. BiFeO3/MXene had appreciable reusability after five adsorption–desorption cycles. Furthermore, BiFeO3/MXene is stable and retains its original properties upon desorption. The present work provides an effective method for eliminating sulfonamides from water by exploiting the excellent texture properties of BiFeO3/MXene.


Introduction
Since the economy and industry have continued to grow, the environment has been severely destroyed, and water pollution has become a serious problem. Protecting water resources and preventing water pollution have become increasingly important in modern society. For example, the presence of organic pollutants in the aquatic environment, such as personal-care products, pharmaceuticals, steroid hormones, industrial chemicals, and pesticides, has caused great concern. It is known that sewage treatment plants, hospitals, and medical wastewater produce organic pollutants in aquatic environments when they are not properly treated [1][2][3][4]. Due to their toxicity to water ecosystems and human health, the presence of these pollutants in wastewater is considered an environmental threat [5]. Sulfonamides are synthetic medicines used to treat and prevent a variety of human and animal diseases [6,7]. Moreover, the use of sulfonamides over a prolonged period or in excess results in their widespread release into the environment, increasing aquatic microorganism resistance, which, in turn, will adversely affect human health through the food chain in future generations [8,9]. In severe cases, it may lead to an imbalance in the body's flora, a malfunction of the digestive system, and even death [10,11]. In addition to posing a serious threat to human health, the ecosystem, as well, is seriously threatened. Therefore, a simple, efficient, and stable method must be developed to remove

Characterizations of Ti 3 C 2 T x MXene and BiFeO 3 /MXene
Ti 3 C 2 T x MXene sheet-like composites were prepared by selectively etching Al from the corresponding MAX phase (Ti 3 AlC 2 ) with hydrofluoric acid (HF), as illustrated in Scheme 1. The shift in the (002) peak to a lower angle and the disappearance of the highest diffraction peak of Ti 3 AlC 2 at 39 • (2Ө) in the X-ray diffraction (XRD) patterns suggest that the Ti 3 AlC 2 was successfully transformed into Ti 3 C 2 T X (Figure 1a). On the obtained Ti 3 C 2 T X was, further, grown BiFeO 3 , using a simple and one-step hydrothermal method. The XRD characterization of the prepared BiFeO 3 /MXene in Figure 1b indicates that the prepared hybrids displayed peaks from MXene and that of BiFeO 3 . In the BiFeO 3 /MXene composite, the characteristic XRD peaks for the BiFeO 3 phase (PDF number: JCPDS086-1518) can be observed, whereas other peaks of rutile-TiO 2 and anatase-TiO 2 were detected as a result of MXene heating above 180 • C [33]. In addition, the appearance of the peak at 10.7 • in both BiFeO 3 /MXene and MXene should be ascribed to the corresponding MAX stack structure remaining after the etching process [34].
Molecules 2023, 28, x FOR PEER REVIEW 3 of 17 observed, whereas other peaks of rutile-TiO2 and anatase-TiO2 were detected as a result of MXene heating above 180 °C [33]. In addition, the appearance of the peak at 10.7° in both BiFeO3/MXene and MXene should be ascribed to the corresponding MAX stack structure remaining after the etching process [34].   observed, whereas other peaks of rutile-TiO2 and anatase-TiO2 were detected as a result of MXene heating above 180 °C [33]. In addition, the appearance of the peak at 10.7° in both BiFeO3/MXene and MXene should be ascribed to the corresponding MAX stack structure remaining after the etching process [34].   Fourier transmission infrared (FTIR) spectroscopy was used to determine the chemical structure and functional groups of the prepared materials, as shown in Figure 1c. All spectra showed the peaks at 1724.3 and 1262 cm −1 assigned to C=O and C-O stretching vibrations, respectively [34]. The band around 3426.7 cm −1 corresponds to the stretching vibration mode of the hydroxyl group (-OH), thus confirming the presence of water molecules. The peaks at 3659.8, 3595.9, and 1632.2 cm −1 in Mxene are related to the -OH bending which had been allocated to adsorb H 2 O, confirming to MXene's hydrophilic character [35]. In addition, the peaks at 568.2 and 455.9 cm −1 are indicative of Fe-O stretching and the bending vibrations of octahedral FeO 6 , indicating the existence of the BiFeO 3 phase [36].
The Raman spectrum of MXene and BiFeO 3 /MXene are presented in the 50-1000 cm −1 region (Figure 1d). Raman spectroscopy provides information about structural phase transitions and lattice properties. As is well-known, there are 13 Raman active modes predicted for the space group R3c and rhombohedral distorted structure [37]. The obtained spectrum was characterized by 4A1 and 3E modes. The 4A1 modes are located at 88.4, 122.6, 241.2, and 458.7 cm −1 while the E modes are located at 305.8, 315.1, and 508.9 cm −1 . The lower frequency modes (<400 cm −1 ) are associated with the Bi-O covalent bond, whereas the higher frequency modes (>400 cm −1 ) are related to Fe-O bonds [38]. However, compared to the pure MXene phase, except for the presence of new apparent peaks from BiFeO 3 , the hybrid shows widening peaks, revealing the interaction between the two phases.
Next, the morphological structure and elemental composition of the prepared BiFeO 3 / MXene are shown in Figure 2. SEM images in Figure 2a,b, indicate the clear difference between the MAX phase and MXene as a result of Al etching from the MAX phase. In contrast to the BiFeO 3 /MXene composite, pure MXene exhibits the characteristic superposed ultrathin sheet structure (Figure 2b), while the latter is decorated with BiFeO 3 nanoparticles on both sides of the material's surface (Figure 2c). Figure 2d presents the typical TEM images of the BiFeO 3 /MXene hybrid; it is clear that BiFeO 3 nanoparticles firmly adhere to the surface of MXene, which is in agreement with the SEM results. The HR-TEM in Figure 2e confirms the crystalline structure of BiFeO 3 , with apparent lattice fringes and a spacing of 0.27 nm corresponding to the (110) plane of the BiFeO 3 phase [36]. Energy dispersive X-ray (EDX) analysis indicated the presence of Bi, Fe, O, Ti, and C ( Figure 2f). It can be seen that the BiFeO 3 nanoparticles disperse evenly on the MXene nanosheets, as shown in energy-dispersive X-ray spectroscopy (EDX) elemental maps ( Figure 2g).
The Brunauer-Emmett-Teller (BET) surface area of MXene was determined to be 3.93 m 2 /g, which increased to 36.24 m 2 /g for BiFeO 3 /MXene. According to the Barret-Joyner-Halenda (BJH) model, the total pore volume of MXene and BiFeO 3 /MXene was 0.021 cm 3 /g and 0.12 cm 3 /g, respectively ( Figure S2, see Supplementary Materials). As can be seen, the surface area of BiFeO 3 /MXene significantly increased, by more than ten times compared to pristine MXene. The hybrid sheet structure of BiFeO 3 /MXene presents an open structure that could make it easier for the adsorbate to reach the more active sites in the BiFeO 3 /MXene. Based on these results, it appears that BiFeO 3 nanoparticles can be grown on MXene using one-step and single-pot techniques, leading to the formation of a BiFeO 3 /MXene hybrid with improved surface area and crystallinity.
The elemental composition and bonding behavior of the BiFeO 3 /MXene were studied using XPS. Figure 3a shows several core peaks of Bi, Fe, O, Ti, and C, indicating that the material is not composed of a single phase. The high-resolution spectrum of Bi 4f (Figure 3b) shows two different characteristic peaks at 158.1 and 163.5 eV, which correspond to the spin-orbit components of Bi 4f 7/2 and Bi 4f 5/2, respectively. According to the literature, this means that bismuth has an oxidation state of 3+ [39,40]. The high-resolution XPS spectrum of Fe 2p (Figure 3c) displayed two main peaks, at 709.8 and 723.4 eV, corresponding to Fe 2p 3/2 and Fe 2p 1/2 , respectively. These two peaks are known to be associated with the ionic states of Fe. The deconvoluted Fe 2p XPS spectrum shows the appearance of peaks and satellite peaks corresponding to the existence of Fe 3+ and Fe 2+ states. The satellite peaks at 717.7 eV are very sensitive to the ionic states of Fe. Therefore, they can also be used to qualitatively determine the oxidation states of Fe. The coexistence of two oxidation states of Fe suggests the presence of oxygen vacancies in the BiFeO 3 /MXene composites, where electron exchange between Fe 3+ -O-Fe 2+ states may stabilize the charge imbalance in the system that emerged due to oxygen vacancies [41]. The XPS spectra of O 1s (Figure 3d) showed three peaks from the curve deconvolution at 528.8, 530.2, and 531.4 eV, which are ascribed to the lattice oxygen of anatase TiO 2 (O−Ti), hydroxyl oxygen(O−H), and surface-adsorbed oxygen species (O−Fe), respectively [42]. The high-resolution spectrum of Ti 2p represents three doublets (Ti 2p 3/2 and Ti 2p 1/2 ) (Figure 3e). The first, at 454.4 and 463.0 eV, the second, at 457.2 and 465.1 eV, and the third, at 460.3 and 470.2 eV, can be attributed to Ti-C, Ti(II), and Ti-O, respectively [43,44]. The XPS spectra of C 1s (Figure 3f) showed the peaks from the deconvolution located at 280.7, 283.8, 284.2, 285.2, 287.6, 291.8, and 294.7 eV which could be assigned to Ti−C, C=C, C−C, C−O, C=O, O=C−OH, and an interaction satellite, respectively [29,45]. In addition, using XPS elemental composition data (at. %), the ratio of BiFeO 3 : MXene was calculated to be 1:4.  The Brunauer-Emmett-Teller (BET) surface area of MXene was determined to be 3.93 m 2 /g, which increased to 36.24 m 2 /g for BiFeO3/MXene. According to the Barret-Joyner-Halenda (BJH) model, the total pore volume of MXene and BiFeO3/MXene was 0.021 cm 3 /g and 0.12 cm 3 /g, respectively ( Figure S2, see Supplementary Materials). As can be seen, the surface area of BiFeO3/MXene significantly increased, by more than ten times compared to pristine MXene. The hybrid sheet structure of BiFeO3/MXene presents an open structure that could make it easier for the adsorbate to reach the more active sites in the BiFeO3/MXene. Based on these results, it appears that BiFeO3 nanoparticles can be grown on MXene using one-step and single-pot techniques, leading to the formation of a BiFeO3/MXene hybrid with improved surface area and crystallinity.
The elemental composition and bonding behavior of the BiFeO3/MXene were studied the second, at 457.2 and 465.1 eV, and the third, at 460.3 and 470.2 eV, can be attributed to Ti-C, Ti(II), and Ti-O, respectively [43,44]. The XPS spectra of C 1s (Figure 3f) showed the peaks from the deconvolution located at 280.7, 283.8, 284.2, 285.2, 287.6, 291.8, and 294.7 eV which could be assigned to Ti−C, C=C, C−C, C−O, C=O, O=C−OH, and an interaction satellite, respectively [29,45]. In addition, using XPS elemental composition data (at. %), the ratio of BiFeO3: MXene was calculated to be 1:4.

Adsorption Kinetics
A study of the adsorption kinetics of BiFeO3/MXene was conducted to predict their adsorption mechanism toward sulfonamides. The adsorption-kinetic data were investigated using pseudo-first-order and pseudo-second-order models, and intraparticle diffusion models. Pseudo-first-order kinetics describes rate-determining processes such as chemical reactions and mass transport. The pseudo-second-order model assumes that the overall adsorption rate of the adsorbate by the adsorbent is chemisorption, while an intraparticle diffusion model illustrates the adsorption mechanism [46][47][48]. Adsorption kinetics were fitted using the following Equations (1)-(3).

Adsorption Kinetics
A study of the adsorption kinetics of BiFeO 3 /MXene was conducted to predict their adsorption mechanism toward sulfonamides. The adsorption-kinetic data were investigated using pseudo-first-order and pseudo-second-order models, and intraparticle diffusion models. Pseudo-first-order kinetics describes rate-determining processes such as chemical reactions and mass transport. The pseudo-second-order model assumes that the overall adsorption rate of the adsorbate by the adsorbent is chemisorption, while an intraparticle diffusion model illustrates the adsorption mechanism [46][47][48]. Adsorption kinetics were fitted using the following Equations (1)- (3).
where q e (mg g −1 ) and q t (mg g −1 ) are the adsorption capacity at equilibrium time and time t (min), respectively; k 1 (g mg −1 min −1 ) is the pseudo-first-order rate constant; k 2 (g mg −1 min −1 ) represents the second-order rate constant; k id (mg g −1 ·min 1/2 ) is the intraparticle diffusion rate constant; and c (mg g −1 ) is the constant that represents the thickness of the boundary layer.
The results of the adsorption kinetics of sulfonamides on BiFeO 3 /MXene are presented in Figure 4 and the related parameters for the fitted models are listed in Table 1. As shown in Figure 4a, the adsorption for the six sulfonamides was very fast during the first 10 min and then became slow, and, finally, reached the equilibrium in 30 min due to the large specific surface area of BiFeO 3 /MXene. Fast adsorption within 10 min was primarily the result of a greater number of active adsorption sites on the surface BiFeO 3 /MXene, while the slowly adsorbed phase was primarily the result of decreasing adsorption sites and electrostatic repulsion between sulfonamides already adsorbed and those in solution. Nevertheless, to ensure equilibrium, the experiment lasted for 240 min. Figure 4b,c presents the pseudo-firstorder and pseudo-second-order models. It can be seen that the pseudo-second-order model fitted much better than the pseudo-first-order model due to their values of R 2 . In addition, the theoretical q e value (11.5, 5.6, 10.9, 13.1, 20.1, and 5.2 mg g −1 for SDZ, STZ, SMZ, SMTZ, SMXZ, and SXZ, respectively) was the closest to the experimental data (10.29, 3.82, 10.01, 11.01, 18.99 and 4.84 mg g −1 for SDZ, STZ, SMZ, SMTZ, SMXZ, and SXZ, respectively) ( Table 1). According to these results, this adsorption is chemisorption rather than mass transport. To investigate the diffusion mechanisms, the experimental data were fitted with the intra-particle diffusion model. The curves in Figure 4d are composed of three linear stages, the presence of multilinearity confirms that intraparticle diffusion is not the only rate-determining step [49]. The first stage involves the rapid diffusion of sulfonamides on the surface of BiFeO 3 /MXene; the second is the diffusion process of sulfonamides molecules into the pore of BiFeO 3 /MXene; the final stage is the chemical bonding which eventually resulted in adsorption equilibrium [50].
As shown in Figure 4a, the adsorption for the six sulfonamides was very fast during the first 10 min and then became slow, and, finally, reached the equilibrium in 30 min due to the large specific surface area of BiFeO3/MXene. Fast adsorption within 10 min was primarily the result of a greater number of active adsorption sites on the surface BiFeO3/MXene, while the slowly adsorbed phase was primarily the result of decreasing adsorption sites and electrostatic repulsion between sulfonamides already adsorbed and those in solution. Nevertheless, to ensure equilibrium, the experiment lasted for 240 min. Figure 4b,c presents the pseudo-first-order and pseudo-second-order models. It can be seen that the pseudo-second-order model fitted much better than the pseudo-first-order model due to their values of R 2 . In addition, the theoretical qe value (11.5, 5.6, 10.9, 13.1, 20.1, and 5.2 mg g −1 for SDZ, STZ, SMZ, SMTZ, SMXZ, and SXZ, respectively) was the closest to the experimental data (10.29, 3.82, 10.01, 11.01, 18.99 and 4.84 mg g −1 for SDZ, STZ, SMZ, SMTZ, SMXZ, and SXZ, respectively) ( Table 1). According to these results, this adsorption is chemisorption rather than mass transport. To investigate the diffusion mechanisms, the experimental data were fitted with the intra-particle diffusion model. The curves in Figure 4d are composed of three linear stages, the presence of multilinearity confirms that intraparticle diffusion is not the only rate-determining step [49]. The first stage involves the rapid diffusion of sulfonamides on the surface of BiFeO3/MXene; the second is the diffusion process of sulfonamides molecules into the pore of BiFeO3/MXene; the final stage is the chemical bonding which eventually resulted in adsorption equilibrium [50].

Adsorption Isotherms
The adsorption isotherm experiments were conducted to predict the adsorption mechanisms and determine the maximum sulfonamide adsorption capacities of MXene and BiFeO 3 /MXene. To simulate the adsorption isotherms, Langmuir and Freundlich isotherm models were used, and the maximum adsorption capacities were calculated based on the constants obtained from these isotherms. The Langmuir isotherm model represents monolayer adsorption, which implies homogeneous surfaces assuming that all absorption sites possess the same affinity for solutes, whereas the Freundlich isotherm model suggests multilayer adsorption based on the adsorption on heterogeneous sites of adsorbents with varying adsorption energies and affinity [42,47]. Adsorption isotherms were fitted using the Langmuir model and Freundlich model using the following, Equations (4) and (5).
where q e (mg g −1 ) and q max (mg g −1 ) represent the equilibrium and maximum adsorption capacity, respectively; KL is the Langmuir constant; KF is the Freundlich constant; and n is the adsorption strength index. The isotherm for the adsorption of sulfonamides on BiFeO 3 /MXene compared to MXene and BiFeO 3 are shown in Figure 5 and the parameters fitted by the Langmuir and Freundlich models are presented in Table 2. These results show that the Langmuir model fits the experimental data well compared to the Freundlich model due to the relatively high values of the correlation coefficient (R 2 ). This implies the monolayer adsorption of these sulfonamides onto BiFeO 3 /MXene, and MXene, due to the presence of a surface-terminated functional groups such as -OH, -H, -O and -F. Additionally, according to Freundlich constants (greater than 1), sulfonamides were favorably adsorbed onto BiFeO 3 /MXene, MXene and BiFeO 3 . The calculated values of maximum adsorption capacities (q max ) in a mixed system show that the BiFeO 3 /MXene composite exhibits a higher adsorption capacity (11.6, 5.6, 10.9, 13.1, 20.1, and 5.2 mg g −1 for SDZ, STZ, SMZ, SMTZ, SMXZ, and SXZ, respectively) than MXene (4.9, 3, 4.3, 6.9, 7.1 and 1.5 mg g −1 for SDZ, STZ, SMZ, SMTZ, SMXZ, and SXZ, respectively) and BiFeO 3 (4.9, 2.8, 3.8, 5.2, 5.7, and 1.3 mg g −1 for SDZ, STZ, SMZ, SMTZ, SMXZ, and SXZ, respectively) under the same experimental conditions. This may be due to the synergistic effect between BiFeO 3 and MXene. In addition, the adsorption capacity of BiFeO 3 /MXene on the six sulfonamides was investigated in a single system and the isotherms are shown in Figure S3. The results show that the maximum adsorption capacity was 32.7, 54.4, 41.3, 37.8, 29.9, and 24.8 mg g −1 for SDZ, STZ, SMZ, SMTZ, SMXZ, and SXZ, respectively ( Table 2). These values are higher than those of mixed-system adsorption due to the competition between different analytes in mixed-system adsorption. Furthermore, Table 3 shows the adsorption capacities reported in the literature using different adsorbent materials. It is seen that BiFeO 3 /MXene had the highest adsorption capacity as a result of its higher surface area as well as higher mesoporous volumes, which may facilitate the adsorption of sulfonamides. of mixed-system adsorption due to the competition between different analytes in mixedsystem adsorption. Furthermore, Table 3 shows the adsorption capacities reported in the literature using different adsorbent materials. It is seen that BiFeO3/MXene had the highest adsorption capacity as a result of its higher surface area as well as higher mesoporous volumes, which may facilitate the adsorption of sulfonamides.

Langmuir Model Freundlich Model
Adsorbents System Analyte q max (mg g −1 )

Effect of Initial pH on the Adsorption Performance
The pH of the solution can have a significant impact on the chemical characteristics and structure of the adsorbent, as well as on the adsorbate itself, during the adsorption process. Additionally, as sulfonamides are amphoteric compounds, their adsorption process is greatly influenced by pH [57]. Therefore, as the pH deviates from its pKa, the sulfonamide's current form will alter and have an impact on the effectiveness of adsorption. The pka of the six sulfonamides are shown in Table S1. When pH < pKa, sulfonamides mainly exist in the form of cations while when pH > pKa, sulfonamides exist in the form of anions. To study the effect of pH on sulfonamides adsorption, experiments were conducted at pH values ranging from 2 to 10. As shown in Figure 6a, the adsorption capacity of BiFeO 3 /MXene increased with the increase in pH and reached the maximum when the pH was 6 for SDZ, STZ, SMZ, and SMTZ and 5 for SMXZ and SXZ. To further understand the effect of pH on the adsorption of the six sulfonamides, the zeta potential of BiFeO 3 /MXene was investigated, as shown in Figure 6b. It can be seen that BiFeO 3 /MXene reached the isoelectric point (PZC) at a pH of about 2.2. Therefore, BiFeO 3 /MXene was positively charged when the pH was less than 2.2 due to the protonation of surface functional groups, and became negatively charged when the pH was greater than 2.2 due to deprotonation. Due to the existence of oxygen-containing functional groups, with the increase in the pH value, the surface of BiFeO 3 /MXene became deprotonated, and the negative charge on its surface enhanced the electrostatic attraction between the material and positively charged sulfonamides, thereby increasing the adsorption capacity. The pH of the solution can have a significant impact on the chemical characteristics and structure of the adsorbent, as well as on the adsorbate itself, during the adsorption process. Additionally, as sulfonamides are amphoteric compounds, their adsorption process is greatly influenced by pH [57]. Therefore, as the pH deviates from its pKa, the sulfonamide's current form will alter and have an impact on the effectiveness of adsorption. The pka of the six sulfonamides are shown in Table S1. When pH < pKa, sulfonamides mainly exist in the form of cations while when pH > pKa, sulfonamides exist in the form of anions. To study the effect of pH on sulfonamides adsorption, experiments were conducted at pH values ranging from 2 to 10. As shown in Figure 6a, the adsorption capacity of BiFeO3/MXene increased with the increase in pH and reached the maximum when the pH was 6 for SDZ, STZ, SMZ, and SMTZ and 5 for SMXZ and SXZ. To further understand the effect of pH on the adsorption of the six sulfonamides, the zeta potential of BiFeO3/MXene was investigated, as shown in Figure 6b. It can be seen that BiFeO3/MXene reached the isoelectric point (PZC) at a pH of about 2.2. Therefore, BiFeO3/MXene was positively charged when the pH was less than 2.2 due to the protonation of surface functional groups, and became negatively charged when the pH was greater than 2.2 due to deprotonation. Due to the existence of oxygen-containing functional groups, with the increase in the pH value, the surface of BiFeO3/MXene became deprotonated, and the negative charge on its surface enhanced the electrostatic attraction between the material and positively charged sulfonamides, thereby increasing the adsorption capacity.

Reusability Study
Reusability is one of the most crucial factors in the development of an advanced and efficient adsorbent. Ideally, a promising adsorbent should have a high adsorption capacity and high desorption efficiency, which will lower its overall cost. In this study, after adsorption, the BiFeO3/MXene powder was removed from the solution by centrifugation. Then, 1 M NaOH solution was used to desorb the sulfonamides from BiFeO3/MXene. To investigate the stability of BiFeO3/MXene, SEM, XRD, XPS and FT-IR, characterizations after desorption were performed. The results indicated that there are no diffraction peaks change. In addition, XPS and FT-IR spectra remain unchanged, highlighting the stability of BiFeO3/MXene ( Figure S4). The recyclability of BiFeO3/MXene up to the fifth cycle is shown in Figure S5; it is observed that the adsorption capacity of BiFeO3/MXene after 5 regenerations at pH 6 was 7.01, 2.07, 7.18, 7.41, 14.07 and 2.06 mg g −1 for SDZ, STZ, SMZ, SMTZ, SMXZ, and SXZ, respectively, and regeneration efficiency of 66.3, 39.2, 70.1, 67.9,

Reusability Study
Reusability is one of the most crucial factors in the development of an advanced and efficient adsorbent. Ideally, a promising adsorbent should have a high adsorption capacity and high desorption efficiency, which will lower its overall cost. In this study, after adsorption, the BiFeO 3 /MXene powder was removed from the solution by centrifugation. Then, 1 M NaOH solution was used to desorb the sulfonamides from BiFeO 3 /MXene. To investigate the stability of BiFeO 3 /MXene, SEM, XRD, XPS and FT-IR, characterizations after desorption were performed. The results indicated that there are no diffraction peaks change. In addition, XPS and FT-IR spectra remain unchanged, highlighting the stability of BiFeO 3 /MXene ( Figure S4). The recyclability of BiFeO 3 /MXene up to the fifth cycle is shown in Figure S5; it is observed that the adsorption capacity of BiFeO 3 /MXene after 5 regenerations at pH 6 was 7.01, 2.07, 7.18, 7.41, 14.07 and 2.06 mg g −1 for SDZ, STZ, SMZ, SMTZ, SMXZ, and SXZ, respectively, and regeneration efficiency of 66.3, 39.2, 70.1, 67.9, 76.8 and 39.6% were achieved for SDZ, STZ, SMZ, SMTZ, SMXZ, and SXZ, respectively, indicating that this adsorbent possesses the capacity of regeneration. However, the decrease in adsorption capacity was due to a reduction in the BiFeO 3 /MXene during the recovery. Therefore, it can be assumed that BiFeO 3 /MXene can be reused for the adsorption of sulfonamides several times with good performance. Moreover, the performance of BiFeO 3 /MXene even after recycling was greater than that of pristine MXene.

Selectivity
BiFeO 3 /MXene was used to remove sulfonamides from actual water samples to test the feasibility of the proposed method. The removal rate of sulfonamides in ultrapure water, tap water, and Yellow-River water by BiFeO 3 /MXene are shown in Figure S6. The results show that removal rates of sulfonamides were in ultrapure water 61.6, 43.9, 72.8, 59.43, 82.5, and 43 .5% for SDZ, STZ, SMZ, SMTZ, SMXZ, and SXZ, respectively, were obtained at the concentration of 10 mg L −1 . This implies a good removal effect on sulfonamides in all samples. In addition, the removal rate follows the order of ultrapure water > tap water > Yellow River water. This may be due to the high level of pollutants competing with sulfonamides for the active sites on the adsorbent in the river water, thus causing a decrease in the sulfonamide removal rate.

Preparation of Ti 3 C 2 T x MXene
A total of 5.0 g of Ti 3 AlC 2 powder was dissolved in an 80 mL aqueous solution of hydrofluoric acid (HF, 4%) under vigorous stirring for 24 h at room temperature. This was performed to selectively etch aluminium. Afterward, the obtained product was centrifuged for 10 min at 3500 rpm, and the supernatant was washed with distilled water many times, each time at 3500 rpm for 5 min, to remove the residual HF and impurities until the pH was close to 6. The obtained precipitate (dark green) was dried in an oven at 70 • C for 12 h to obtain the Ti 3 C 2 T x MXene powder.

Preparation of BiFeO 3 /MXene
The BiFeO 3 /MXene was synthesized by a single-step hydrothermal process as shown in Scheme 1. First, 0.01 mol Bi(NO 3 ) 3 ·5H 2 O and Fe(NO 3 ) 3 ·9H 2 O were dissolved in 40 mL KOH (10 M) as a mineralizer with a stirring process for 30 min. A total of 0.6 g of MXene were added and continually stirred for 1h. Then, the solution was transferred to a sealed Teflon-lined autoclave and heated at 200 • C for 6 h. The reacted sample was washed 5 times with ethanol and distilled water sequentially, and dried in an oven at 70 • C for 8 h to obtain BiFeO 3 /MXene powder.

Characterizations
The crystal structure was examined using X-ray diffraction diffractometer (X'pert PRO, PANalytical, Almelo, The Netherlands). The BET-specific surface area, pore diameter, and pore size were determined via the N 2 adsorption-desorption isotherms at 77 K with a surface area (ASAP 2010, Micromeritics, Norcross, Georgia, USA). The morphologies were studied by field emission scanning electron microscope (FESEM) (JSM-6701F scanning elec-tron microscope, JEOL, Tokio, Japan) and transmission electron microscope (TEM) (Tecnai G2TF20, FEI, Hillsboro, Oregon, USA). The functional groups were characterized using Fourier transmission infrared spectroscopy (FTIR) (model IFS120HR, Bruker, Karlsruhe, Germany) equipped with a DTGS detector, collecting 32 scans per sample at a resolution of 4 cm −1 and Raman spectroscopy (model IFS120HR, Bruker, Germany). Zeta potential was determined using a Zeta sizer Nano-ZS90 dynamic light scattering instrument (Malvern, Britain). X-ray photoelectron spectroscopy (XPS, ESCALAB 250Xi, Thermo Fisher Scientific, Waltham, Massachusetts, USA) was used to identify the electronic state and chemical bonding at the surface of the synthesized samples. The concentration of sulfonamides was measured by high-performance liquid chromatography (HPLC, 1260 Infinity series, Agilent Technologies, Santa Clara, California, USA).

Adsorption Experiments
The adsorption of sulfonamides on BiFeO 3 /MXene was carried out using a batch experimental process. As a typical adsorption experiment, 20 mg of BiFeO 3 /MXene was suspended in a centrifuge tube containing 10 mL of sulfonamides at pH 6 and was continuously shaken at room temperature for 24 h using a rotary shaker. The samples were then filtered through a 0.22 µm filter and HPLC analysis was performed. The obtained chromatogram is shown in Figure S1. For the isotherm study, the initial concentration of sulfonamides varied from 0 to 100 mg L −1 while for the kinetic study, the contact time varied from 0 to 240 min. The adsorbed amounts of sulfonamides were calculated as follows (Equation (6)) where q e (mg g −1 ) is the adsorption capacity at equilibrium time, C 0 (mg L −1 ) is the concentration of sulfonamides in solution before adsorption, C e (mg L −1 ) is the concentration of sulfonamides in solution after adsorption, V (L) is the volume of sulfonamides solution.

Conclusions
A BiFeO 3 /MXene composite was synthesized using a single-step hydrothermal method and was used for the adsorption of sulfonamides from an aqueous solution. The batch adsorption experiments were carried out to study the adsorption of BiFeO 3 /MXene towards sulfonamides and the data were systematically evaluated using kinetic models and isotherm models. The pseudo-second-order model fits the experimental data well, according to kinetic models. In addition, BiFeO 3 /MXene showed the rapid adsorption of sulfonamides and attained equilibrium within 10 min, while the Langmuir model was well-fitted using isotherm models. BiFeO 3 /MXene exhibited an adsorption capacity of 32.7, 54.4, 41.3, 37.8, 29.9, and 24.8 mg g −1 for SDZ, STZ, SMZ, SMTZ, SMXZ, and SXZ, respectively, which is higher compared to pristine MXene, BiFeO 3 , and previously reported adsorbent materials. This may be due to the synergistic effect of BiFeO 3 /MXene and MXene. Furthermore, the adsorption behavior was explained mainly by electrostatic attraction between the surface functional groups of BiFeO 3 /MXene and the sulfonamides molecules. The BiFeO 3 /MXene composite had excellent reusability and remarkable selectivity in actual water samples. This research should shed new light on how to design adsorbents that effectively remove sulfonamides from environmental water.