Atrazine, 6-chloro-N2-ethyl-N4-isopropyl-1,3,5-triazine-2,4-diamine, is a widely used triazine herbicide used for controlling annual grasses and broadleaf weeds (Solomon et al., 1996). Due to its persistence, moderate aqueous solubility (35 mg/L), high mobility, and long half-life, atrazine has a high detection rate in surface water, groundwater, and soil (Tappe et al., 2002; Qu et al., 2017; Zheng et al., 2019). In the Hubei Province of central China, atrazine was detected in the sediments of six eutrophic lakes, and the highest concentration of atrazine was found to be 0.171 mg/kg in Honghu Lake (Qu et al., 2017). Atrazine was also detected in two soils in Belgium and Germany (8.3 and 15.2 μg/kg, respectively), even in soils not treated with atrazine (Jablonowski et al., 2010). In addition, atrazine has been categorized as an endocrine disruptor and a probable human carcinogen, which may affect the central nervous system and immune systems and even affect human semen quality and fertility (Hayes et al., 2003; Swan et al., 2003; Chen et al., 2009). Atrazine has been banned in some European countries, but it is still widely used in China. Therefore, it is necessary to develop a reliable and effective treatment to remove or sequester atrazine from aquatic environment and farmland soil to reduce the environmental and health risk of atrazine.
Biochar, a carbon-rich solid material, is produced by pyrolysis of biomass with limited or without oxygen (Novak et al., 2009). As an excellent remediation agent, biochar has been widely used in wastewater and soil to immobilize or sequester pesticides, such as herbicides and insecticides, through sorption, partition, and pore diffusion (Zheng et al., 2010; Yu et al., 2011; Li et al., 2018). Liu et al. (2015) reported that soybean biochar has much higher atrazine removal ability in aqueous solution. Jin et al. (2016) indicated that biochar would be helpful to stabilize soil contaminated with imidacloprid, isoproturon, and atrazine. Our previous research found that peanut shell biochar also had a good sorption effect on atrazine (Wang et al., 2020). Therefore, biochar can effectively reduce the environmental risk of atrazine. Many studies have shown that the degradation degree of pesticides in soil is different after adding biochar. Generally, biochar-amended soil increases sorption of pesticides and reduces bioavailability of soil to microorganisms, which reduces the biodegradation of pesticides and prolongs the half-life of pesticides (Yang et al., 2010; Yu et al., 2011; Li et al., 2017b). However, some studies have found that the organic matter of biochar can enhance the biological activity of microorganisms by providing nutrients so as to accelerate the degradation of pesticides (Fang et al., 2016; Wu et al., 2019). Singh et al. (2022) found that the addition of biochar to the soils increased the half-life of atrazine and significantly improved the recovery process of soil biological activities under atrazine stress.
Recently, the combination of biochar and clay has been widely used for pollutant removal in order to improve the structure and sorption characteristics of biochar (Zhang and Gao, 2013; Yao et al., 2014; Tang et al., 2015). Clay minerals are abundant natural resources with inexpensive, high surface area, cation exchange capacity, and structural properties. Montmorillonite (MMT) is the most commonly studied clay material, which is an irregular lamellar crystal composed of layers of one octahedral and two tetrahedral sheets (Zhu et al., 2019). The fine particles of MMT are unsuitable for water treatment, but in a composite form, biochar has a good porous structure to support MMT (Chen et al., 2017). In addition, MMT could provide exogenous metal atoms (i.e., aluminum and magnesium), which may be embedded to react with biochar, forming a high-performance biochar complex (Song et al., 2020). The composite makes full use of the good sorption capacity of biochar and MMT to become a low-cost and effective sorbent. However, research on the effect of MMT/BC on sorption and degradation of contaminants, as well as on the removal of contamination from aqueous solution and soil, was scarce.
Therefore, the aims of this study were to (1) develop a low-cost and effective MMT–biochar composite by using a simple and low-cost method, (2) assess the ability and mechanisms of atrazine removal from aqueous solutions, and (3) evaluate the effects of MMT–biochar composite on the sorption and degradation of atrazine in different soil. This study provides useful information for better evaluation of the potential of biochar–clay composite in reducing pesticide residues.
Materials and Methods
Reagents and Chemicals
Standard atrazine (purity 99.2%) was obtained from Shenyang Research Institute of Chemical Industry (Shenyang, China). HPLC-grade acetonitrile, formic acid, and sodium azide (NaN3) were purchased from Sigma-Aldrich (Steinheim, Germany). All analytical reagents including calcium chloride (CaCl2), sodium chloride (NaCl), anhydrous magnesium sulfate (MgSO4), sodium hydroxide (NaOH), and hydrochloric acid (HCl) were obtained from Sinopharm Chemical Reagent Co., Ltd (Beijing, China). MMT was purchased from Shanghai Macklin Biochemical Co., Ltd (Shanghai, China). Ultrapure water was prepared using a Milli-Q reagent water system (Bedford, MA, United States).
Biochar and Soil Preparation and Characterization
Peanut shells were collected from the Shandong Province of China, washed with tap water to remove the surface dust and soil, dried at 70°C, and then crushed by using a high-speed pulverizer and passed through an 18-mesh sieve. A stable MMT suspension was prepared by adding MMT powder to 100 ml ultrapure water and mixed with ultrasound for 30 min. Then, 20 g peanut shells were immersed in MMT suspensions, stirred by magnetic stirrer for 2 h, and dried in oven at 105°C for 12 h. The impregnated samples were placed in a quartz boat of a tubular furnace (Zhonghuan Experimental Furnace Co., Ltd., Tianjin, China), pyrolyzed in a continuous flow of N2, heated at a rate of 5°C/min, and maintained for 1 h when the pyrolysis temperature reached 600°C. The produced biochar samples were crushed, passed through an 80-mesh sieve, stored in a brown ground glass bottle, and sealed in a dryer. In total, five types of MMT–biochar composites were prepared by changing the mass ratio of MMT to BC (i.e., 20, 25, 30, 40, and 50%), and the resulting products were designated as 20% MMT/BC, 25% MMT/BC, 30% MMT/BC, 40% MMT/BC, and 50% MMT/BC, respectively. At the same time, peanut shells were treated with the same method to prepare BC as control. Unless otherwise specified, the MMT/BC mentioned later is 25% MMT/BC. By changing the pyrolysis temperature, MMT/BC under different temperature conditions was prepared, and the pyrolysis temperature was set to 400, 500, and 600 °C, respectively.
Elemental analysis using surface structure, scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectrometer (XPS) was based on our previous analysis methods (Wang et al., 2020). Transmission electron microscopy (TEM) (FEI, Thermo Fisher Scientific, United States) was used to observe the microstructure of the biochar. Zeta potential of biochar was determined using a Zetasizer Nano ZS90 (Malvern Instruments, Malvern, United Kingdom). The pH value of the solution was measured by using a pH meter (FiveEasy Plus, Mettler Toledo, United States).
Two kinds of agricultural soil without detectable atrazine were collected from Jilin (44°23′52″N, 125°10′2″E) and Shandong provinces (36°12′43″N, 116°41′29″E) of China, denoted as S-DB and S-SD, respectively. The soils were taken at the top 10 cm and screened by using a 2 mm sieve for sorption and degradation experiments. The physicochemical properties of the S-DB showed it to be sandy loam (65.4% sand, 15.1% silt, and 19.5% clay) with pH 7.83, 41.0 g/kg organic matter, 1.15% organic carbon, and 17.2 cmol (+)/kg CEC. The S-SD also belonged to sandy loam (57.9% sand, 17.3% silt, and 24.8% clay) with pH 7.24, 29.2 g/kg organic matter, 0.39% organic carbon, and 21.4 cmol (+)/kg cation exchange capacity (CEC).
Sorption Experiments of Biochar in Aqueous Solution
To determine the effect of MMT dosage (0, 20, 25, 30, 40, and 50%) and pyrolysis temperature (400, 500, and 600°C) on the removal of atrazine, 100 mg biochar and 40 ml of 10 mg/L atrazine aqueous solution (contained 0.01 mol/L CaCl2 and 200 mg/L NaN3) were introduced into 50 ml brown sample bottles. The bottles were then sealed and shaken in the dark on a reciprocating shaker at 180 rpm and 25 ± 1°C for 72 h. The pH of the mixtures was adjusted to 7.0 ± 0.2 using 0.1 M HCl/NaOH and monitored during and after sorption. The same conditions were used to test the effects of initial pH in the range of 2–9 on MMT/BC sorption. After the experiments, the bottles were put to rest for 10 min to make the biochar samples sink into the bottom by gravity to achieve solid–liquid separation, and the supernatant was filtered using a 0.22 μm membrane filter. The filtered solutions were then stored at −20°C until analysis.
The sorption kinetic and isotherm of atrazine were carried out on BC and MMT/BC using the same conditions and procedures, as described before. The kinetic tests were conducted with an initial atrazine concentration of 10 mg/L, 150 mg of BC, or 50 mg of MMT/BC per 40 ml atrazine solution. Duplicate bottles were sampled at predetermined times (1, 2, 4, 6, 8, 10, 12, 24, 48, and 72 h) and analyzed for atrazine concentration in the solution. In the sorption isotherm experiment, 150 mg BC or 50 mg MMT/BC was mixed with 40 ml atrazine solution with the concentration of 0.25–30 mg/L for 72 h.
Under the same conditions, the solutions without biochar were set for the control test. The loss of atrazine was negligible, including hydrolysis and sorption on the bottle wall. Based on the initial and final concentration of atrazine in solution and the dosage of biochar, the sorption capacity of atrazine on biochar was calculated.
Sorption Experiments on Soil and Biochar–Soil Mixtures
The sorption isotherms of atrazine on biochar and biochar–soil mixtures were determined by three repeated batch sorption experiments under eight initial concentrations of atrazine (0.25–30 mg/L). A 5 g aliquot of soil with or without 50 mg BC or MMT/BC was weighed into a 50 ml centrifuge tube. Then, 25 ml of the background solution containing 0.01 M CaCl2 and 200 mg/L NaN3 was added. According to the initial concentration, a certain amount of atrazine stock solution was added to the centrifuge tube, the cover was tightened, and then shaken for 72 h at 180 rpm and 25 ± 1°C in the dark. At the end of the experiment, the tubes were centrifuged at 4,000 rpm for 10 min, and 1.5 ml of supernatant was filtered into the injection vial through 0.22 μm membrane filter. The filtered solutions were stored at −20°C until analysis.
Before the degradation experiments, a part of the collected soil was pre-cultured with a moisture content of 60% of the water holding capacity in the dark incubator (25 ± 1°C) for 2 weeks, and the other part was sterilized at 121°C for 30 min in an autoclave (Lead-Tech Scientific Instruments Co., Ltd, Shanghai, China). MMT/BC was chosen to investigate the impacts on atrazine degradation in the two soils. First, an aliquot of 20 g soil (dry weight) or the biochar–soil mixture (4 g of MMT/BC) was weighed into a 500 ml glass bottle, and then 100 μL of the atrazine acetone stock solution (10,000 mg/L) was added into the bottle. The soil samples were kept for 10 min until the acetone volatilized completely and then vortexed for 5 min. Next, another 180 g soil was weighed into the bottle, vortexed for 30 min, and mixed well with the spiked soil; the final concentration of atrazine in soil was 5 mg/kg (dry weight). After that, 15 g of spiked soil was weighted into 50 ml pre-cleaned glass bottle, and the soil moisture content was adjusted with ultrapure water to 60% of the saturated soil moisture content. In the same operation, the sterilized ultrapure water containing 200 mg/L NaN3 was added into the sterilized soil to inhibit the growth of microorganisms. The bottles were stoppered with cotton and cultured in the dark in an incubator under constant temperature (25 ± 1°C) and humidity (70%). The water content was monitored regularly during soil incubation to maintain the initial state of soil moisture. Triplicate sample bottles of each treatment were removed after predetermined incubation times (0, 1, 3, 5, 7, 14, 21, 30, 40, 60, 90, and 120 days), and the soil samples were freeze-dried and stored at −20°C until extraction. Details of the soil sample treatment are shown in Supplementary Text S1.
where qt and qe represent the amount of atrazine removed at time t and at equilibrium, respectively (mg/kg); k1 and k2 are the sorption rate constants (1/h); α represents the initial sorption rate (mg/kg); and β represents the desorption constant (kg/mg).
where qe represents the atrazine concentration on the solid-phase at equilibrium (mg/kg), Ce represents the solution concentration of atrazine at equilibrium (mg/L), Kf [(mg/kg)/(mg/L)n] and K (L/mg) represent affinity coefficient, n represents the Freundlich linearity constant, b represents the affinity constant (L/mg), KD represents the partition domain coefficient (L/kg), and qm and Q represents the maximum capacity (mg/kg).
The first-order reaction kinetic model was used to fit the data of atrazine degradation kinetics in soil and biochar–soil mixtures (Zhang et al., 2018):
where C0 is the initial concentration of atrazine (mg/kg), Ct is the concentration of atrazine (mg/kg) at sampling time t (d), k is the degradation rate constant (d−1), and the half-life (t1/2) was ln2/k.
The experimental data were fitted by Origin 9.1. The statistical analyses were analyzed by SPSS 25.0 one-way analysis of variance (ANOVA).
Results and Discussion
Characterization of Biochar
The properties of biochar varied greatly between BC and MMT/BC. The elemental composition (C, N, H, and O) of BC and MMT/BC, presented in Table 1, suggested that the addition of MMT reduced the content of C, N, H, and O, especially the carbon content, from 87.35% to 50.91%. The surface area of MMT/BC was slightly decreased from 262.86 to 233.16 m2/g, which may be related to the pore coating or plugging caused by the existence of MMT minerals (Yao et al., 2014). The total pore volume and the average pore diameter of the MMT/BC were increased from 0.014 to 0.066 cm3/g and 4.44–12.02 nm in comparison with BC. This is probably because MMT is layered silicate mineral, which contains mineral elements with small surface areas and abundant transitional pores (Li et al., 2015; Li et al., 2017a; Yao et al., 2014). The N2 adsorption–desorption isotherms and pore size distribution of MMT/BC and BC are shown in Supplementary Figure S1. As described by the International Union of Pure and Applied Chemistry (IUPAC), the isotherms of BC evolved to type I, which shows the characteristic of a microporous material (Jing et al., 2014). The N2 isotherms of MMT/BC resemble those of type Ⅱ, and the observed hysteresis curves of MMT/BC is of type H4, indicating the narrow cracks and pores in the sorbent materials (Jing et al., 2014). In the pore size distribution curve (Supplementary Figure S1B), BC and MMT/BC exhibited heterogenous pore structures, and mesopore (2–50 nm) was the main pore structure.
The SEM images of BC and MMT/BC are shown in Figures 1A,B. Surface and pore filling mechanisms may be responsible for the removal of atrazine as the pores were observed on biochar surfaces. The SEM images of MMT/BC clearly showed that MMT particles adhered to the biochar surface and completely coated the pure biochar, changing the surface morphologies and providing more sorption sites (Liang et al., 2019; Premarathna et al., 2019). Also, the MMT did not block the pores of biochar, which ensures the accessible to the adsorbate molecules (Premarathna et al., 2019). TEM imaging of the MMT/BC (Figure 1D) showed that the biochar surface was widely covered by the layered structures compared with BC (Figure 1C). In addition, it is reported that the structure is a common clay structural morphology (Tyagi et al., 2006; Zhou et al., 2009).
As shown in FTIR (Figure 2), the spectrum at ∼3,400 cm−1 showed stretching vibrations of O-H, ∼1,580 cm−1 was related to stretching vibration of C=C of the aromatic ring (Chen et al., 2008; Keiluweit et al., 2010). The band observed around 1,050 cm−1 was related to the Si-O functional groups on the MMT/BC surface (Tyagi et al., 2006; Chen et al., 2017). The bands appearing below 800 cm−1 of MMT/BC could be attributed to Si-O stretching, Si-O-Mg bending, Si-O-Al bending, and Si-O-Si bending (Zhou et al., 2009; Chen et al., 2017).
Raman spectra (Supplementary Figure S2) showed two prominent peaks at ∼1,350 cm−1 and ∼1,600 cm−1, representing D-band originated from sp3 hybridization with disordered mode and G-band induced by crystalline graphitic/sp2 carbon stretching vibrations with the tangential mode, respectively (Ferrari and Robertson, 2000; Akhavan, 2010). The higher ratio of ID/IG peak intensity means higher defect concentration and increased functional groups on the sorbents surface. The ID/IG decrease from 1.04 for BC to 1.00 for MMT/BC, which was not a significant change.
Zeta potentials of MMT/BC are depicted in Supplementary Figure S3. In the pH range between 2 and 9, the MMT/BC resulted in a zeta potential drop of 35 mV. The MMT/BC surface was negatively charged at pH values greater than the point of zero charge pH (pHpzc, 2.7) and was positively charged at pH values lower than pHpzc (Nandi et al., 2009).
The full XPS spectra representing the chemical composition and crystalline states are displayed in Figures 3A,E. For MMT/BC, the six peaks at 285.0, 400.0, 532.6, 74.0, 103.2, and 1,304.3 eV were attributed to the element of C, N, O, Al, Si, and Mg on the surface, respectively, while there are no obvious peaks corresponds to Al, Si, and Mg on the surface of BC. The high-resolution C 1s spectra (Figures 3B,F) could be deconvoluted into four peaks: C-C/C-H (∼284.8 eV), C-O (∼286.4 eV), C=O (∼288.0 eV), and O-C=O (∼289.5 eV) (Gao et al., 2018; Liu et al., 2015). The O 1s spectra (Figures 3C,G) could be attributed into three groups: C=O (∼531.6 eV), -OH (∼532.5 eV), and C-O (∼534.1 eV) (Lyu et al., 2017b; Zhou et al., 2007). The N 1s spectra of BC (Figure 3D) can be deconvoluted into two peaks at 398.7 and 400.6 eV, which can be assigned to the pyridinic N (C-N=C) and pyrrolic N (C-N). A new peak corresponding to graphitic N can be found at 402.0 eV for MMT/BC (Figure 3H) (Jansen and Van Bekkum, 1995; Lyu et al., 2017a; Mueller et al., 2015). Supplementary Table S1 listed their relative percentages on BC and MMT/BC. For C 1s, the C-O ratio of biochar increased from 8.74% to 12.09% after MMT was added, and the C=O ratio increased from 4.52% to 4.98%, indicating the participation of oxygen-containing functional groups (Liang et al., 2019). For O 1s, the -OH ratio of biochar increased from 42.47% to 67.22% after MMT was added, and the effect of MMT/BC on atrazine had hydrogen bond involvement.
FIGURE 3. XPS spectra of BC (A–D) and MMT/BC (E–H). (A,E) Wide survey scan, (B,F) C 1s, (C,G) O 1s, (D,H) N 1s.
Sorption of Atrazine on Biochar
Effects of MMT Dosage
The effects of MMT rate during biochar preparation on the removal efficiency of atrazine were investigated. As shown in Figure 4A, the removal efficiency of atrazine significantly (p < 0.05) increased from 16.01% (BC) to 52.78% (25% MMT/BC) with an increase of the MMT contents from 0 to 25%, suggesting a 36.77% increase. However, relatively lower removal efficiencies were obtained by other dosage (20, 30, 40, and 50%), suggesting 29.89%–33.90% increase compared to the control (BC). The surface of BC coated with MMT led to its larger pore size and volume (Table 1), especially the reactive surface area and CEC (Yao et al., 2014; Chen et al., 2017); therefore, the combination of MMT and biochar is particularly effective in the removal of atrazine. However, the excessive clay particles could block the pores of biochar, resulting in the decrease of available sorption sites and sorption capacity of the composite (Yao et al., 2014; Fosso-Kankeu et al., 2015). Therefore, 25% MMT was the best ratio of composite materials, and 25% MMT/BC was selected for sorption experiment and identification of sorption mechanism in aqueous solution, as well as sorption and degradation experiments in soils.
FIGURE 4. Effects of MMT dosage during biochar preparation (A) and pyrolysis temperature of MMT/BC (B) on atrazine removal efficiency. Values with lowercase letters are different from each other (p < 0.05), and values with capital letters are significantly different from each other (p < 0.01).
Effects of Pyrolysis Temperature
As shown in Figure 4B, with the increase of pyrolysis temperature, the removal efficiency of atrazine by MMT–biochar composites increased from 44.72% (400°C) to 53.71% (500°C) and 78.50% (600°C). Our previous study (Wang et al., 2020) found that in the low concentration (about <15 mg/L) the sorption capacity of peanut shell biochar for atrazine increased with the increase of pyrolysis temperature. The results showed that biochar composites are also affected by pyrolysis temperature, 600°C was taken as the pyrolysis temperature of MMT/BC. This temperature was also used to prepare clay–biochar composite materials by Yao et al. (2014).
Sorption Kinetics of Atrazine on Biochar
Sorption kinetics of atrazine on BC and MMT/BC are shown in Figures 5A,B. The kinetics experiment data showed that the uptake of atrazine by BC and MMT/BC increased rapidly from 0 to 496.00 and 1,353.49 mg/kg in the first half hour, respectively, and increased steadily after 12 h (620.75 mg/kg for BC and 1819.39 mg/kg for MMT/BC). In order to determine the atrazine sorption equilibrium, the next experiment time was determined as 72 h.
FIGURE 5. Sorption kinetics (A,B) and sorption isotherms (C,D) of atrazine on BC and MMT/BC. Kinetic data were fitted to first-order, second-order, and Elovich models. Isotherm data were fitted to Freundlich, Langmuir, and dual-mode models. Error bars indicate SD.
The corresponding fitting parameters and the coefficient of determination (R2) values are shown in Table 2. Compared with the first-order and second-order sorption kinetic models, the Elovich models fit the experimental data better with R2 > 0.97 (0.974 for BC and 0.988 for MMT/BC); the second was second-order (0.909 for BC and 0.914 for MMT/BC), and the worst was first-order (0.836 for BC and 0.848 for MMT/BC). The results revealed that atrazine sorption to the BC and MMT/BC was controlled by multiple mechanisms (Yao et al., 2014).
TABLE 2. Fitting parameters of sorption kinetics and sorption isotherms of atrazine on BC and MMT/BC.
Sorption Isotherms of Atrazine on Biochar
Sorption isotherms of atrazine on BC and MMT/BC are shown in Figures 5C,D. All three isotherm models fit the data well, and the parameters are shown in Table 2. The dual-mode model has better fitting performance than Freundlich and Langmuir, with R2 of 0.992 for BC and 0.996 for MMT/BC. The results revealed that sorption of atrazine on BC and MMT/BC was mainly partition and surface adsorption (Tang et al., 2015). Compared to BC, the Q value of atrazine on MMT/BC was increased from 592.99 to 1920.18 mg/kg. Therefore, the maximum capacity of MMT/BC on atrazine was about 3.2 times greater than that of BC. Hence, the modification method of MMT in this study could effectively improve the performance of biochar.
Effects of Solution pH
The effects of pH on atrazine sorption by MMT/BC are presented in Supplementary Figure S4. The sorption capacity was strongly affected by the initial pH of the aqueous solution. In brief, the uptake of atrazine decreased from 2,337.98 (pH = 2) to 1,292.89 mg/kg (pH = 9), with the increase of the pH value. It has been reported that the solution pH may change the degree of ionization of pesticide molecule, surface charge, and extent of dissociation of functional groups on the active sites of the biochar (Nandi et al., 2009). Atrazine is a weak alkaline pesticide with pKa value of 1.7, mainly exists as neutral molecule in the environment of pH 5–9, and promotes the formation of triazine cation at very low pH (Zheng et al., 2010). The MMT/BC surface was negatively charged at pH > 2.7, and it was combined with the triazine cations of atrazine by electrostatic interaction. Moreover, triazine cation could be exchanged with interlayer hydrated cations (Na+ and Ca2+) to enter the interlayer space of MMT (Premarathna et al., 2019). Therefore, the sorption capacity of MMT/BC to atrazine under low pH was high. At high pH, sorption was barely influenced by pH; this was similar to the result of Tan et al. (2016). Although, physisorption dominated, chemical sorption by chemical bonding and the increase of effective binding area caused by MMT deposition on the surface of biochar also promoted the sorption (Premarathna et al., 2019).
Sorption Mechanism Analysis
For both the BC and MMT/BC, the aromatic carbon on the surface of biochar can used as both an electron acceptor and an electron donor. The heterocyclic ring in atrazine is a π electron donor, so atrazine can interact with biochar through π-π electron donor–acceptor interactions (Sun et al., 2010; Zhao et al., 2013). Atrazine could also be used as hydrogen donors and acceptors to form hydrogen bonds with H, N, or O on the surface of biochar, further enhancing the sorption affinity of biochar. For both BC and MMT/BC, the sorption of atrazine is mainly chemical interactions, such as π–π interaction, hydrogen bonding, ion exchange, and electrostatic interactions. Due to the porosity of biochar, physical sorption may also be carried out via pore filling mechanism. In addition, the high surface activity and interlayer spaces of MMT improved the sorption capacity of MMT/BC for atrazine through both surface sorption and intercalation interactions. So, MMT/BC was an effective adsorbent to remove atrazine from aqueous solution compared with BC.
Sorption of Atrazine on Soils and Biochar–Soil Mixtures
The sorption isotherms (Figure 6) were fitted using the Freundlich model (Eq. 4), and the parameters of the atrazine in two agricultural soils and biochar–soil mixtures are shown in Table 3. The Freundlich model can well describe the sorption data of atrazine (R2 > 0.98). It was well documented that organic matter affects the sorption potential of soils, and higher organic matter content leads to more contaminants sorption (Fenoll et al., 2011). The organic matter contents of S-DB and S-SD were 41.0 and 29.2 g/kg, respectively, so the Kf of S-DB [19.01 (mg/kg)/(mg/L)n] was higher than that of S-SD [16.71 (mg/kg)/(mg/L)n]. The addition of biochar increased the sorption affinity of atrazine in soil, and the effect of MMT/BC is more obvious. For S-DB, the addition of BC increased Kf to 31.08 (mg/kg)/(mg/L)n and the addition of MMT/BC increased to 57.35 (mg/kg)/(mg/L)n; for S-SD, the addition of BC increased Kf to 36.32 (mg/kg)/(mg/L)n and the addition of MMT/BC increased to 60.48 (mg/kg)/(mg/L)n. The n values for biochar-amended soils were less than that of unamended soils, which indicated that the degree of isotherm non-linearity increased after biochar amendment, especially MMT/BC. Due to the non-linearity of the isotherms, the distribution coefficients (Kd) of three equilibrium concentrations (Ce = 0.05, 0.5, and 5 mg/L) were calculated (Table 3). Similar to Kf, the Kd of the soil was also increased with biochar amendment, and the Kd values of all the soils and biochar–soil mixtures decreased with increasing atrazine concentration. Previous studies have shown that water-soluble organic matters could be sorbed by biochar and compete with the added organic matter for limited sorption site or pores of biochar, thus reducing the sorption capacity of biochar (Cornelissen et al., 2005; Koelmans et al., 2009). However, organic substances may diffuse through the humic layer into biochar micropores overtime (Pignatello et al., 2006). Obviously, in the current research, atrazine may reach the micropores of biochar through the humic layer, thus improving the sorption capacity of atrazine.
FIGURE 6. Sorption isotherms of atrazine onto soil, BC-soil mixtures, and MMT/BC-soil mixtures [(A): S-DB; (B): S-SD). Isotherm data were fitted to Freundlich model.
Degradation of Atrazine in Soil and Biochar–Soil Mixtures
The degradation parameters of atrazine in soils and biochar–soil mixtures for 120 days under sterilized and non-sterilized conditions are shown in Table 4. The degradation curves of atrazine in non-sterilized S-DB and S-SD were fitted well with the first-order reaction kinetics model (R2 > 0.96), and the half-lives were 29.1 and 40.5 days, respectively. The degradation of atrazine in S-DB was faster than that in S-SD; the main reason could be the high content of organic matter in S-DB, which can serve as an energy source to stimulate microbial activities and accelerate the degradation of pesticides (Gavrilescu, 2005; Briceño et al., 2007). However, in sterilized soils, the half-lives increased to 341.5 and 521.2 days, indicating that soil microbial was the main reason for atrazine degradation. After MMT/BC addition, the half-lives of atrazine in the non-sterilized soils increased (from 29.1 to 97.8 days for S-DB and 40.5 days to 126.7 for S-SD) and the degradation amount decreased (from 89.39% to 60.54% for S-DB and 81.69%–59.13% for S-SD). Previous studies have shown that biochar application in soil could reduce the biodegradation of pesticides (such as atrazine, acetochlor, diuron, and acetamiprid) by enhancing its sorption to the soil (Yang et al., 2006; Loganathan et al., 2009; Yu et al., 2011; Li et al., 2018) because the sorbed pesticides can only be biodegraded after being desorbed by the soil and diffused into the soil solution (Yu et al., 2011). The strong sorption of atrazine by MMT/BC made atrazine difficult to desorb, and atrazine was not easy to be degraded by microorganism; therefore, the degradation of atrazine was delayed. For sterilization treatment, the addition of MMT/BC accelerated the degradation of atrazine, indicating that biochar promoted the chemical degradation. It has been proved that biochar can also affect the chemical degradation of pesticides; Zhang et al. (2018) reported that the active groups on the biochar mineral surface played an important role in the chemical degradation of thiacloprid in biochar–soil mixtures. However, the mechanism of atrazine chemical degradation by MMT/BC remains to be further studied.
In this study, a montmorillonite–biochar composite (MMT/BC) was prepared via slow pyrolysis of MMT pretreated peanut shells for atrazine remediation. Structure and morphology analysis of raw biochar (BC) and MMT/BC showed that MMT particles have been successfully coated on the surface of biochar. However, excessive MMT particles will reduce the sorption capacity of biochar; 25% MMT was the best ratio of composite materials. MMT/BC was also affected by pyrolysis temperature; the higher the temperature (600°C), the better the sorption effect. Sorption experiments indicated that MMT/BC has higher removal capacity of atrazine than that of BC. The sorption of atrazine to MMT/BC was depended on pore-filling, π–π interaction, hydrogen bonding, ion exchange, and electrostatic interactions, and the high surface activity and interlayer spaces of MMT also improved the sorption capacity of MMT/BC through both surface sorption and intercalation interactions. In addition, the amendment of MMT/BC in soil improved the sorption capacity and delayed the degradation of atrazine. The results showed that MMT-modified biochar was a promising soil amendment to control atrazine contamination. According to the sorption and degradation mechanism of biochar and soil properties, it provided a basis for the selection of an effective biochar sorbent.
Data Availability Statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
PW: conceptualization, methodology, data curation, formal analysis, investigation, validation, and writing—original draft. MS, LW, SY, LM, LZZ, LZ, YZ, and HJ: supervision. YZ: conceptualization, resources, supervision, and project administration. XL: supervision. resources, project administration, writing—review and editing, and funding acquisition.
This work was supported by the National Natural Science Foundation of China (32102269 and 31861133021).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors, and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fenvs.2022.888252/full#supplementary-material
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