Original Research ARTICLE
Preparation of Carboxymethyl Cellulose-Based Macroporous Adsorbent by Eco-Friendly Pickering-MIPEs Template for Fast Removal of Pb2+ and Cd2+
- 1Key Laboratory of Clay Mineral Applied Research of Gansu Province, Center of Eco-Material and Green Chemistry, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou, China
- 2College of Petroleum and Chemical Engineering, Beibu Gulf University, Qinzhou, China
- 3Department of Chemical Engineering, College of Petrochemical Engineering, Lanzhou University of Technology, Lanzhou, China
Recently, Pickering high internal phase emulsions (Pickering HIPEs) have been widely used to fabricate macroporous materials. However, the high usage of poisonous organic solvent in HIPEs not only greatly increases the cost but also is harmful to human health and environment, which leads to limited large-scale applications. In this study, we prepared a novel monolithic macroporous material of carboxymethyl cellulose-g-poly(acrylamide)/montmorillonite (CMC-g-PAM/MMT) by the free radical polymerization via oil-in-water Pickering medium internal phase emulsions (Pickering MIPEs), which used the non-toxic and eco-friendly flaxseed oil as continuous phase, MMT, and Tween-20 (T-20) as stabilizer. The pore structure of the resulting macroporous materials could be tuned easily by adjusting the content of MMT, co-surfactant T-20, and the oil phase volume fraction. The maximal adsorption capacities of the prepared macroporous material for Pb2+ and Cd2+ were 456.05 and 278.11 mg/g, respectively, and the adsorption equilibrium can be reached within 30 min. Otherwise, the macroporous monolith exhibited excellent reusability through five adsorption–desorption cycles. Thus, the eco-friendly Pickering-MIPEs is a potential alternative method to be used to fabricate multi-porous adsorption materials for environmental applications.
Graphical Abstract. Preparation of macroporous adsorbent from Pickering MIPEs for removal of heavy metal.
Recently, macroporous materials with high porosity and good interconnectivity have attracted much attention in many fields, such as catalysts (Pierre et al., 2006; Zhang et al., 2008; Chan-Thaw et al., 2010; Pulko et al., 2010; Kovačič et al., 2014; Wang et al., 2014), tissue engineering scaffolds (Busby et al., 2001; Zhang et al., 2005; Hu et al., 2014; Viswanathan et al., 2015), ion exchange columns (Zhao et al., 2007; Alexandratos, 2008), electrode materials for energy storage (Liu et al., 2008; Kou et al., 2011), and water purification (Yu et al., 2015; Zhu et al., 2016c; Wu et al., 2017). Thus, many methods have been used to prepare macroporous materials. Among these technologies, the emulsion template may be the most effective method to prepare the macroporous polymer with extraordinary advantages, including a well-defined pore structure, a controllable pore size, as well as inherent high porosity (Xu et al., 2015). The most well-known emulsion template technology is the high internal phase emulsions (HIPEs), which, with an internal phase volume of >74% and the prepared macroporous polymers, are also termed poly-HIPEs.
Conventional HIPEs are commonly stabilized with a large amount of surfactants (5–50 vol % with respect to the continuous phase) (Zheng et al., 2014). Inevitably, the heavy use of these surfactants significantly increases the high cost of materials (Wu et al., 2012). Thus, more and more studies involving HIPEs have focused on the Pickering HIPEs, which employ a small amount of solid particles substituting surfactants partially or totally to stabilize emulsions (Binks and Lumsdon, 1999). In addition, the macroporous poly-HIPEs created from Pickering HIPEs often have improved mechanical strength (Silverstein, 2014), additional features, and functions, due to the introduction of solid particles, such as magnetic property, photocatalytic performance, and so on (Vílchez et al., 2011).
Despite the fact that macroporous poly-HIPEs prepared from Pickering HIPEs have these excellent properties, some problems still need to be solved. Firstly, the macroporous poly-HIPEs prepared from Pickering-HIPEs, which are only stabilized by solid particles, often have closed-cell voids and super porous structures with void sizes of 200–700 μm (Ikem et al., 2010a,b, 2011). The weak permeability and the low surface area limit the application of the macroporous materials in many fields, especially in water treatment. Secondly, it also should be noted that oil/water (O/W) HIPEs often require more than 74% of organic solvent (such as toluene, n-hexane, p-xylene, liquid paraffin, and so on) in disperse phase. The wide use of these organic solvents greatly increases the cost as well as the threat to human health and environment. Thus, discovery of a new strategy, which can reduce the oil phase volume and replace the poisonous organic solvent with eco-friendly natural oil for preparation of the macroporous materials with interconnected pore structure via emulsion template is very meaningful.
Compared with HIPEs, medium internal phase emulsions (MIPEs, V < 74%) require less organic solvents and decrease the diameter of the emulsion droplet, which is beneficial in increasing material surface area. Ikem et al. (2010b, 2011) have reported that introducing a small amount of surfactant (~5% of the continuous phase volume) to stabilize Pickering HIPEs cooperatively with particles before polymerization will reduce the void sizes of the poly-Pickering HIPEs and results in materials with large pore throats and permeability. Otherwise, the permeability and connectivity of the poly-MIPEs can be adjusted by changing the content of nanoparticles or introducing an appropriate amount of surfactant (Wang et al., 2017a,b). According to the preceding discussion, in this study, we reported a new strategy for fabrication of macroporous material from Pickering-MIPEs, which is stabilized by montmorillonite (MMT) together with nonionic surfactant, and non-toxic low-cost flaxseed oil was used as emulsion in disperse phase. MMT, being a natural silicate clay mineral with abundant -OH groups and negatively charged, is highly hydrophilic; thus, MMT silicate clay can be used to stabilize O/W emulsion without any further modification to regulate its wettability (Shen et al., 2006; Dong et al., 2014). To the best of our knowledge, most of the present research on clay mineral-stabilized emulsion focus on the stability of emulsion or on the preparation of microspheres with Pickering emulsion polymerization. Studies involving preparation of highly macroporous polymer monoliths via clay mineral-stabilized Pickering emulsion template are rare. T-20 used in this study was a co-stabilizer emulsion and contributes to formation materials with connected pores. In this research, the pore structure of the prepared macroporous monolith was studied by tuning of MMT and Tween-20 (T-20) concentration and O/W ratio. The potential practical application of the macroporous polymer monoliths in the removal of heavy metal ions (Pb2+ and Cd2+) from aqueous solution was also explored (Graphical Abstract).
Sodium carboxymethylcellulose (CMC, chemical pure, with a viscosity of 300–800 mPa·s), ammonium persulfate (APS, analytical pure), and Tween-20 (T-20, analytical pure) were purchased from BASF Corporation. Na-MMT clay mineral with a cation exchange capacity (CEC) of 90 mEq/100 g was purchased from Southern Clay Products Inc. Flaxseed oil (FO, food grade) was purchased from the Lanzhou Yong Fan Shang Mao company (Lanzhou, China). Acrylamide (AM, chemical pure) was purchased from Shanpu Chemical Factory (Shanghai, China) and used without further treatment. N, N′-methylenebisacrylamide (MBA, chemical pure) was received from Yuan fan additives plant (Shanghai, China). Other reagents were all analytical pure and all solutions were prepared with distilled water.
Preparation of Pickering Emulsion
In order to guarantee that MMT dispersed completely in water, the MMT was initially prepared as a suspension with a certain concentration. Briefly, 10 or 15 g of MMT was added into 100 mL of deionized water and sonicated with BILON-650Y Sonifier for 30 min. In the preparation process of the Pickering emulsion, 10 mL of water containing a certain amount of MMT and an appropriate amount of T-20 was stirred at 300 rpm for 2 h in the boiling flask-3-neck in the continuous phase. Then, a determined volume of flaxseed oil was added into the continuous phase and emulsified with a GJD-B12K homogenizer at 11,000 rpm for 5 min.
Preparation of the Macroporous Monolith
The macroporous monolith was prepared via the free radical polymerization in the Pickering emulsion template. Firstly, a Pickering emulsion containing 0.05 g of CMC and 0.23 g of MBA was prepared according to the section Preparation of Pickering Emulsion. Subsequently, 2.13 g (30 mmol) of AM and 138 mg of APS were added into the as-prepared emulsion and rapidly stirred (11,000 rpm) for 1 min. Later, the emulsion was transferred into 10-mL centrifuge tubes and immersed in a 65°C water bath for 24 h to polymerize. After that, the obtained polymerization product was sectioned and washed with acetone by Soxhlet extraction for 12 h and then immersed into 0.5 mol/L NaOH aqueous alcohol solution (Vwater/Valcohol = 3/7) for 24 h to transfer the amide group to carboxyl. The redundant NaOH was washed with alcohol–water solution repetitively. Finally, the macroporous polymer was dried at 60°C for 4 h and named CMC-g-PAM/MMT. The feed compositions and the corresponding pore parameters of all the macroporous monoliths are listed in Table 1.
Table 1. Feed composition of the macroporous monolith and their corresponding average pore size (D) and surface area (A).
The droplet diameters were estimated by counting 200 droplets by using Image Pro Plus as a software tool. The morphologies of the samples were characterized by a field emission scanning electron microscope (SEM, JSM-6701F, JEOL) after coating the samples with gold film. Photographs of Pickering-MIPEs were recorded by iPhone. The infrared (IR) spectra were recorded on a Nicolet NEXUS FTIR spectrometer in the range of 4,000–400 cm−1 using KBr pellets.
Batch Adsorption Studies
The adsorption experiments were performed by immersing 20-mg macroporous monolith into 25 mL Pb2+ or Cd2+ solutions and shocking in a thermostatic shaker (THZ-98A) at 120 rpm at 30°C for a given time to reach adsorption equilibrium. After the adsorption, the concentrations of Pb2+ and Cd2+ solutions were analyzed by a UV–visible spectrophotometer (UV-3010, HITACHI). The adsorption capacity qe (mg/g) of the macroporous monolithic adsorbents was calculated according to the following equation:
where C0 and Ce are the initial and the final concentration of the Pb2+ and Cd2+, V is the volume of the Pb2+ and Cd2+ solution, and m is the adsorbent dosage.
The required pH of solution was adjusted by 0.1 mol/L HCl or NaOH solutions. The adsorption isotherms were conducted by adding adsorbents (Sample 6) into Pb2+ and Cd2+ solutions for 2 h with concentration in the 100–600 mg/L range, and the control factors of the adsorption process were evaluated with the Langmuir and the Freundlich isotherm model. The adsorption kinetics were determined with 400 mg/L Pb2+ and Cd2+ solutions by varying the adsorption time from 5 to 120 min, and the pseudo-first-order equation and pseudo-second-order equation were carried out to describe the adsorption process. All adsorption experiments were repeated thrice to guarantee the accuracy of the obtained data.
The desorption studies were performed to evaluate the recyclability of the macroporous adsorbent. After the adsorption process, the adsorbents were separated and immersed into 30 mL of HCl solution (0.5 mol/L) for 2 h to desorb and then activated with 0.5 mol/L NaOH solution for 2 h. After that, the adsorbents were washed with distilled water till neutral pH and used in the next adsorption process. The adsorption–desorption cycle was performed five times.
Results and Discussion
Preparation and Structure Characteristics of CMC-G-PAM/MMT
Formation of Pickering Emulsion and the CMC-G-PAM/MMT
As shown in Figure 1a, the paste-like concentrated Pickering emulsion (Figure 1a) was prepared by adding dropwise flaxseed oil into the aqueous phase, with MMT and T-20 as the stabilizer. Firstly, the MMT interacted with Tween-20 and formed the surfactant-coated MMT, and then the coated MMT clay particle combined with each other in the water phase to create a 3D network called the “cards house” aggregation model. Because the flaxseed oil is yellow, the Pickering MIPEs were canary yellow. The emulsions can stay in the reversed glass tube without any flow, suggesting that the formed emulsion is a typical gel emulsion and the oil drop is closely packed, which is verified by its optical micrograph as shown in Figure 1c. It can also be observed that the size of oil drops varies from around hundreds of nanometers to several micrometers. The type of emulsion was detected by the pendant-drop method; as presented in Figure 1b, the emulsion droplet dispersed into the distilled water but remained round in toluene, indicating that the emulsion is an O/W emulsion.
Figure 1. (a) Digital photographs of the prepared Pickering MIPEs (MMT, 5%;T-20, 4%; internal phase volume, 50%). (b) Testing the type of emulsion by dropwise adding the emulsion droplet into the distilled water (DI) or toluene. (c) Optical images of the Pickering MIPEs. (d) Digital photographs of CMC-g-PAM/MMT before Soxhlet extraction. (e) Digital photographs and (f) SEM of porous CMC-g-PAM/MMT.
The porous monoliths of CMC-g-PAM/MMT were synthesized by free radical polymerization with APS as the initiator. The sulfate anion radicals formed from the decomposition of APS under 65°C, and the -OH groups of CMC were activated and formed the macro-radicals. Then, the macro-radicals triggered the double bonds of AM and in situ initiated the grafting reaction of the vinyl monomers onto the CMC in the presence of the cross-linker MBA. Once the polymerization reaction ended, the prepared wet monoliths were cut into pieces (Figure 1d) and Soxhlet extracted by acetone to remove off the oil phase, and the end product of white monoliths were finally obtained after drying (Figure 1e). The macroporous polymer monoliths will finally be used as adsorbent to remove heavy metal ions from water; thus, the amide group of the monoliths must be hydrolyzed with NaOH solution to generate -COO-, based on the fact that -COO- groups are easier to combine with heavy metal ions than the acylamino. Because of the hydrogen-bond interaction between polar groups (Zhu et al., 2016a), the prepared monoliths can swell rapidly in the water and shrink during the drying process. In order to avoid pore collapse, hydrolysis was conducted in a NaOH alcohol water mixture (Vethanol/Vwater = 7/3) (Zhu et al., 2016c). Then, the obtained CMC-g-PAM/MMT was dehydrated by Soxhlet extraction with acetone again and dried in an oven at 40°C. A photograph of the final resulting CMC-g-PAM/MMT was shown in Figure 1e. Figure 1f showed the CMC-g-PAM/MMT with a well-interconnected macroporous texture. It could be observed that both the macropores and highly interconnected small pores coexisted in the resulting material. The large cell pores were generated by removal of the oil droplets, and the pore throat derives from the thinnest points of the two neighboring oil drops attributed to the shrinkage during polymerization (Zhu et al., 2016c). The introduction of MMT not only stabilized the emulsion but also participated in polymerization to dramatically improve the performance and mechanical stability of the polymer-based composite (Schexnailder and Schmidt, 2009; Shibayama, 2012).
Effect of MMT Concentration on the Macroporous Structure
We prepared a series of macroporous monoliths from Pickering emulsion, which stabilized with different amounts of MMT particles from 3 to 9% according to the volume of disperse phase. As shown in Figure 2, the enrichment of macrospores can be observed in the matrix of the monoliths. Besides, the surface morphologies of the monolithic materials changed obviously with increasing MMT content from 3 to 9%. The average pore sizes of the prepared monoliths were 1.52, 3.37, 2.75, and 1.89 μm, respectively, corresponding to MMT content that varied from 3, 5, 7, and 9% (Table 1). In the case of 3% MMT, T-20 may play a dominant role for stabilizing the emulsion. When the content of MMT increased to 5%, most of the MMT may be coated with T-20 and then fixed at the O/W interface (Ye et al., 2018). The large size of the coated MMT can only stabilize the droplet larger than T-20; thus, the pore size of macroporous monoliths increased obviously. It was worthy to note that the pore throats existed obviously when 3% MMT was used, but disappeared while increasing the amount of MMT to 5%. This phenomenon has also been found in Pickering emulsions stabilized by other solid particles (Yi et al., 2016), indicating that the pore throats can only form at a moderate ratio of MMT and Tween-20. With an MMT content beyond 5%, the larger interfacial area of emulsion will be stabilized and thus the droplet size decreased. The macropore and pore throat void size distribution of the macroporous monolith with different MMT concentrations was shown in Figure S1.
Figure 2. SEM of macroporous CMC-g-PAM/MMT with different MMT. Three percentage (a, a1, Sample 1); 5% (b, b1, Sample 2); 7% (c, c1, Sample 3); 9% (d, d1, Sample 4).
In general, the increase in particle content will result in smaller droplet size and close packing of droplets, thus leading to more open pores during polymerization. However, as shown in Figure 2, the porous monoliths had a closed pore structure when the amount of the MMT increased from 5 to 9% (Samples 2, 3, and 4). The corresponding possible mechanism was presented in Figure 3. Once the content of MMT increased, the MMT particles packed on the O/W interface around the emulsions closely to form a solid barrier and prevent coalescence (Horozov, 2008). The increase in MMT will lead the aggregation of solid particles at the O/W interface to form a thicker particle layer, which results in a difficult fracture of polymerized film between two adjacent droplets. Thus, it is difficult to obtain monoliths with a desired interconnected structure when a high concentration of the stabilizer is used. These similar results have also been reported by Pickering emulsions stabilized by other solid particles (Wong et al., 2011; Zou et al., 2013b).
Figure 3. Mechanism for the formation of CMC-g-PAM/MMT with closed-cell structure or open-cell structure by adding the MMT and T-20.
Effect of Surfactant Concentration on the Macroporous Structure
Co-surfactant concentration is also an important parameter for tuning the porosity and interconnectivity of macroporous materials prepared from Pickering emulsion template (Zhang et al., 2009, 2011; Zhu et al., 2010). The increase in co-surfactant concentration will decrease the interfacial tension and contribute to form the interconnected pore's structure simultaneously (Viswanathan et al., 2014). We therefore explored the effect of T-20 content on the microstructure of the macroporous monolith with internal phase volumes at 50% for all the starting emulsions; the SEM images were shown in Figure 4. When T-20 increased from 2% (Sample 2) to 3% (Sample 5), the average diameter of the macropore decreased dramatically from 3.37 to 1.43 μm (Table 1). Further increasing T-20 content from 3% (Sample 5) to 6% (Sample 8), it could be observed that the size of the macropore decreased, the number of pore throats per pore structure increased, and the wall thickness of the polymer layer got thin. Moreover, the surface areas of macropores and the pore throats were all increased as the T-20 content increases (Table 1). When T-20 content increased to 6%, a thin-wall macroporous material with perfect porosity was obtained. It is because more surfactant micelles remained at the O/W interface as T-20 content increases, which contributed to reducing the droplet size of Pickering MIPEs and resulted in forming the interconnected pores (Zou et al., 2013a). The corresponding possible mechanism was shown in Figure 3. The macropore size and the pore throat void size distribution of the macroporous monolith with various T-20 contentions were presented in Figure S1.
Figure 4. SEM of the macroporous CMC-g-PAM/MMT monolith with different Tween-20. (a, a1) 2% (Sample 2); (b, b1) 3% (Sample 5); (c, c1) 4% (Sample 6); (d, d1) 5% (Sample 7); (e, e1) 6% (Sample 8).
Effect of Volume Fraction of Disperse Phase on the Macroporous Structure
The pore size and interconnectivity of the macroporous materials are influenced significantly by the internal phase fraction. The macroporous materials prepared from different oil phase fractions of 50, 40, 30, and 20 vol % are presented in Figure 5. With the oil phase volume fraction decreasing, the macropore size increased and the number of pore throat decreased. When the internal phase volume fraction was 20%, the number of macro- and interconnected pores decreased significantly, while the interconnected pore still existed. This phenomenon indicated that the closely packed pore was not the only reason for forming the interconnected pore. Actually, MMT particles and the surfactant will both absorb onto the O/W interface, and the interconnected pore can also be formed at the interface stabilized by the surfactant (Zhu et al., 2016b). The macropore size and pore throat void size distribution of the prepared macroporous monoliths with variation of oil phase volume fraction were shown in Figure S1.
Figure 5. Effect of oil phase volume fraction for the CMC-g-PAM/MMT (a, a1) 50% (Sample 6); (b, b1) 40% (Sample 9); (c, c1) 30% (Sample 10); (d, d1) 20% (Sample 11). All of the prepared samples prepared with 5% of MMT and 4% of T-20.
The macroporous monoliths were synthesized by free radical polymerization with APS as the initiator. The sulfate anion radicals formed from the decomposition of APS under 65°C, and the –OH groups of CMC was activated and formed the macro-radicals. Later, the macro-radicals triggered the double bonds of AM and in situ initiated the grafting reaction of the vinyl monomers onto the CMC in the presence of cross-linker MBA. Figure 6 showed the FTIR spectra of (a) AM, (b) CMC, and CMC-g-PAM/MMT (c) before and after hydrolysis reaction (d). As can be seen, the band at 3,433 cm−1 in Figures 6C, D was attributed to the characteristic absorption peak of O–H and intermolecular hydrogen bonds of the polysaccharide. The narrow band of C = C stretching vibration at 1,612 cm−1 in the AM spectrum disappeared after polymerization (Figure 6C). Besides, the band at 1,673 cm−1 in the AM spectrum that was ascribed to the vibration of C = O of amide was merged with the strong band (1,603 cm−1) of carboxylate asymmetric vibration in the CMC spectrum and formed a strong and broad absorption band at 1,666 cm−1 in Figure 6C. After the hydrolysis of macroporous monoliths in the alkaline solution (Figure 6D), the absorption peak at 1,666 cm−1 weakened, and the asymmetric stretching vibration (1,562 cm−1) and symmetrical stretching (1,407 cm−1) vibration of -COO− strengthened. All of these proved that AM had been grafted onto CMC and a majority of acid amide groups were transformed into carboxylate groups after the hydrolysis (Ghorai et al., 2014).
Figure 6. FTIR spectra of (A) AM, (B) CMC, CMC-g-PAM/MMT (C) before and (D) after hydrolysis reaction.
Figure 7. Effect of pH on the adsorption capacity of the macroporous monolith (Sample 6) for (A) Pb2+ and (B) Cd2+, respectively. Adsorption conditions: C0, 200 mg/L; dosage of adsorbent, 20 mg/25 mL.
Evaluation of Adsorption Properties
Effect of pH on Adsorption for Pb2+ and Cd2+
The adsorption property of adsorbents for metal ions depends on the charge of binding sites and the metal species present in the solution. Therefore, the pH values of the metal ion solution and isoelectric point (pH of zero point charge, pHIEP) of the prepared porous adsorbent (Sample 6) were determined to better understand the adsorption process. The pHIEP, which represents the net external charge on the surface of the adsorbent in solution (Chingombe et al., 2005), was found to be about 4.0 for Sample 6 (Figure 8A). The adsorption property of the macroporous monolithic adsorbent for the heavy metal ions was investigated in different pH solutions ranging from 1 to 6. As shown in Figure 7, it can be found that the adsorption of Pb2+ and Cd2+ increased quickly at pH 1–4 and then remained constant. Figure 8 showed that the surface of Sample 6 was positively charged at pH lower than pHIEP, while at pH > pHIEP, the surface of Sample 6 was negatively charged. Under acidic conditions, the adsorbents are usually protonized. When pH < 4.0, the protonation of the functional groups resulted in the adsorbent being positively charged and thus rejecting adsorption of Pb2+ and Cd2+, leading to lower adsorption capacity. As the pH increases, the protonation of the functional groups decreases, thus increasing the adsorption capacity. At pH > 4.0, the negatively charged adsorbent attracts the metal cations to increase adsorption capacity until all the active sites were occupied, and then the saturation adsorption was reached.
Figure 8. (A) Zeta potential of CMC-g-PAM/MMT at different pH values. Adsorption experiments: C0, 200 mg/L; t, 1 h; dosage of adsorbent, 50 mg/20 mL. (B) Initial and equilibrium pH of the solutions. Adsorption experiments: C0, 200 mg/L; t, 1 h; dosage of adsorbent, 20 mg/25 mL.
Here, it also should be noted that after the adsorption, the equilibrium pH values of the Pb2+ and Cd2+ solution were all higher than the initial pH (Figure 8B). Under acidic conditions, along with the adsorption process, the -COO− and -CONH2 groups were protonated and converted to -COOH and -, which consumes H+ of the solution, thus increasing the pH. The above discussion indicated that the electrostatic and complexation interactions mainly contribute to the adsorption process (Sitko et al., 2016). Taking into account that the adsorbent had high adsorption capacity for metal ions at high pH, but metal ions will precipitate at excessive high pH, the next adsorption experiments were performed at natural pH.
Effect of Initial Concentration on Adsorption for Pb2+ and Cd2+
The saturation adsorption capacities of the macroporous monoliths for Pb2+ and Cd2+ were evaluated, and the results were shown in Figure 9. The increase in initial metal ions concentrations led to a sharp increase in adsorption capacities, and then the increasing trend became flat until adsorption saturation was reached. The reason was that the driving force at the solid–liquid interface improved with an increase in the initial metal ion concentration, which accelerated the diffusion of metal ions in the matrix and adsorbents. The maximum adsorption capacities of the macroporous monoliths were 456.05 mg/g for Pb2+ and 278.11 mg/g for Cd2+.
Figure 9. Effect of the initial (A) Pb2+ and (B) Cd2+ concentration on the adsorption capacity of macroporous monolith (Sample 6). Adsorption conditions: dosage of adsorbent, 20 mg/25 mL; pH, natural.
The adsorption process was analyzed by the Langmuir (Equation 2) and Freundlich isotherm models (Equation 3) (Gan et al., 2018), and the equations are shown as follows:
where Ce (mg/L) represents the equilibrium concentration of metal ions, and qm and qe are the amounts of metal ions adsorbed per unit mass of adsorbent at equilibrium state at any time (mg/g), respectively. b (L/mg) is the Langmuir constant related to the affinity of binding sites, K is the Freundlich constant related to adsorption capacity, and n represents the index of adsorption intensity or surface heterogeneity.
The isotherm parameters and linear correlation coefficients (R2) for the two models were calculated and summarized in Table S1. The adsorption capacities calculated by the Langmuir model for Pb2+ and Cd2+ were 464.91 and 315.82 mg/g, respectively. The calculated results were closer to the experiment value. Otherwise, all the adsorption isotherm data were better fitted to the Langmuir isotherm model (R2 > 0.99) than the Freundlich model. Thus, the Langmuir model was suitable to describe the adsorption process, which means that the binding sites distributed over the adsorbent surface was homogeneous and these binding sites had the same affinity for adsorption of a single molecular layer (Wen et al., 2012; Wang et al., 2013).
Effect of Contact Time on Adsorption for Pb2+ and Cd2+
The adsorption rate is a key parameter for practical applications. Thus, the effect of contact time on the adsorption behavior was investigated. Figure 10 showed the kinetic adsorption curves of the macroporous monoliths with different oil phase volume fraction for Pb2+ and Cd2+. The adsorption rate of the macroporous monoliths for the metal ions increased remarkably in the first 30 min for Pb2+ and Cd2+. In particular, Sample 6 and Sample 9 with well-interconnected pore structure showed fast adsorption rate. This was because the interconnected pores reduced the mass transfer resistance efficiently and exposed more carboxyl groups (as the binding sites for metal ions), which facilitate the accessibility of metal ions to the adsorbent. However, a large decrease in the adsorption rate was observed when the adsorbent with a relatively small number of macro- and interconnected pores and Sample 11 (prepared with 20% of internal phase volume) reached the equilibrium more than 1 h. The above facts proven that the structure of the adsorbents dramatically affected the adsorption kinetics of the macroporous monoliths for the metal ions. The high porosity and permeability of the adsorbent can improve the adsorption rate.
Figure 10. Adsorption kinetic curves of the macroporous monolith with various oil phase volume fraction for (A) Pb2+ and (B) Cd2+. Adsorption conditions: C0, 400 mg/L; dosage of adsorbent, 20 mg/25 mL; pH, natural.
In order to examine the dynamic adsorption process, the adsorption data were fitted by pseudo-first-order (Equation 4) and pseudo-second-order (Equation 5) (Wu et al., 2018) kinetic models. The kinetic models' equations are expressed as follows:
Here, qt is the amount adsorbed for Pb2+ and Cd2+ at time t and qe is the amount of metal ions by unit mass of adsorbents at equilibrium state. k1 (min−1) and k2 [g/(mg min)] are the adsorption rate constants of the pseudo-first-order and pseudo-second-order models, respectively. The corresponding adsorption kinetic parameters are listed in Tables S2, S3. As shown in Tables S2, S3, the linear correlation coefficients (R2) for the pseudo-second-order kinetic model were much higher than those for the pseudo-first-order kinetic model. Otherwise, the adsorption capacities calculated with the pseudo-second-order kinetic model (qe,cal) were much closer to the experiment values (qe,exp). Thus, the pseudo-second-order kinetic model fit the dynamic adsorption process well and it was controlled mainly by a chemical adsorption process (Zhou et al., 2014).
Regeneration and Reusability
The reusability of the as-prepared macroporous monolith was tested by repeating the adsorption–desorption cycle using 0.5 mol/L HCl as the desorbing agent and 0.5 mol/L NaOH as regeneration solution. As shown in Figure 11, the adsorption capacity had no obvious decrease with increasing the adsorption–desorption cycle. The regenerated monolith still showed high adsorption capabilities for Pb2+ and Cd2+ after being reused five times. Moreover, it should be noted that, after metal adsorption, the adsorbent still maintained a well-porous structure (Figure 12), and it also can be seen from Table 2 that the qm values of the macroporous monolith prepared in this study were much higher than those of the adsorbents reported previously. All the adsorption dates indicated that the as-prepared macroporous monolith materials were an efficient adsorbent for heavy metal ions and had potential application in purification of wastewater.
Figure 11. Adsorption capacity of the macroporous monolith (Sample 6) for (A) Pb2+ and (B) Cd2+ after regenerated five times. Adsorption conditions: C0, 400 mg/L; adsorbent dosage: 20 mg/25 mL; pH, natural.
FTIR and XPS of CMC-g-PAM before and after adsorption of Pb2+ and Cd2+ would provide powerful evidence to clarify the adsorption mechanism of metal ions onto the functional groups of the as-prepared adsorbent. As can be seen from the FTIR spectra in Figure 13, after adsorption of Pb2+ or Cd2+, the strong absorption band at 3,434 cm−1 assigned to the O–H stretching vibration shifted to 3,411 cm−1, indicating the electrostatic interaction and H-bonding between -OH and Pb2+ or Cd2+. Besides, the band at 1,674 cm−1 ascribed to the vibration of C = O of carboxyl, and the asymmetric stretching vibration of -COO− at 1,562 cm−1 shifted to 1,663 and 1,535 cm−1 after adsorption, which proved that the combination of carboxyl and metal ions reduced electron cloud density of oxygen atoms on carboxyl. According to the above, it can be confirmed that the carboxyl group and the hydroxyl group are the main force of the adsorbent to adsorb metal ions.
The XPS spectra of CMC-g-PAM/MMT before and after adsorption were depicted in Figure 14, and the corresponding parameters were listed in Table 3. As the survey spectrum in Figures 14B,C showed, the appearance of Pb 4f and Cd 3d at 139.48 and 412.38 eV after adsorption revealed that the Pb2+ and Cd2+ were specifically adsorbed onto the prepared porous adsorbent. In the high-resolution XPS spectra of C 1s, there were also obvious changes in integral area ratio and binding energy after adsorbing Pb2+ and Cd2+. As listed in Table 3, the integral area ratios of C = O and C–O were both increased, while the integral area ratio of C–C decreased. The shift of binding energy can also be observed in the spectra, especially for the binding energy of C = O and C–O, which can be attributed to the decreased electron density of the adjacent O atoms, and thus the binding energy of the C atoms increased (Ma et al., 2019). The high-resolution O 1s spectra before adsorption presented three peaks at a binding energy of 532.83, 532.05, and 531.24 eV, which are assigned to the C–O, O–H, and C = O groups, respectively. After the adsorption of heavy metal ions, the binding energy increased; meanwhile, the integral area ratio of C = O and C–O decreased, and the integral area ratio of O–H increased. The shift of binding energy was attributed to the complexation between metal and -OH and -COO−, in which O atoms donate electrons to metal ions and the electron density toward O atoms in these groups decrease, thus increasing the binding energy of O 1s peaks. The above results demonstrate that the -COO− and -OH groups in porous adsorbent participate in the adsorption of heavy metal ions, but in different ways (Luo et al., 2014). Otherwise, the weak signal peak of N 1s in the XPS spectra showed that there was only a slight amount of acylamino existing in the materials after hydrolysis. As the high-resolution XPS spectra of N 1s shown, the binding energy of -NH2 and -NHCO- increased slightly, while their integral area ratio decreased after the adsorption of heavy metal ions, demonstrating that the acylamino groups participated in the adsorption process. These results revealed the electrostatic attraction or coordination interaction between the functional groups and heavy metal ions, and the COO− and -OH groups provide the main adsorption sites. The acylamino groups assisted in the adsorption process.
A series of novel macroporous monolithic adsorbents had been successfully prepared by polymerization of Pickering MIPEs with natural MMT and T-20 as the stabilizer and the non-toxic and eco-friendly flaxseed oil used in disperse phase. The structure of the macroporous monolith can be adjusted by changing the volume of oil phase and the content of MMT and T-20. The synergistic effects of MMT and T-20 were favorable to create the macroporous monolith materials with a closed-cell or highly interconnected macroporous structure. The prepared macroporous monoliths showed fast adsorption kinetics for Pb2+ and Cd2+, and the adsorption equilibrium can be reached as fast as 30 min. Otherwise, the adsorption rate of the adsorbent can be improved by increasing the connectivity and porosity of the monolith. The adsorption capacities of the adsorbent for Pb2+ and Cd2+ were 456.05 and 278.11 mg/g, respectively. In addition, the macroporous monolith exhibited excellent reusability. After five adsorption–desorption cycles, the regenerated monolith still had good absorbability and maintained a well-porous structure. As a whole, we provided a new approach to fabricating macroporous monoliths that are highly efficient and recyclable using a type of eco-friendly Pickering MIPE. The prepared monoliths can be used as efficient adsorbent for the removal of heavy metals from wastewater.
The datasets generated for this study are available on request to the corresponding author.
FW and YZ contributed to the experiment process and data analysis, wrote the paper, and created all the figures. HX contributed to the design of the experiment, data analysis, and revision of the paper. AW contributed to the experiment design, data analysis, and revision of the paper.
The authors are grateful for the financial support from the National Natural Science Foundation of China (21706267), the Major Projects of the National Natural Science Foundation of Gansu, China (18JR4RA001), the Funds for Creative Research Groups of Gansu, China (17JR5RA306), and the Scientific Research Project of Beibu Gulf University, China (17KYQD57).
Conflict of Interest Statement
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.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fchem.2019.00603/full#supplementary-material
Ahmad, M., Manzoor, K., Chaudhuri, R. R., and Ikram, S. (2017). Thiocarbohydrazide cross-linked oxidized chitosan and poly(vinyl alcohol): a green framework as efficient Cu(II), Pb(II), and Hg(II) adsorbent. J. Chem. Eng. Data 62, 2044–2055. doi: 10.1021/acs.jced.7b00088
Busby, W., Cameron, N. R., and Jahoda, C. A. (2001). Emulsion-derived foams (PolyHIPEs) containing poly (ε-caprolactone) as matrixes for tissue engineering. Biomacromolecules 2, 154–164. doi: 10.1021/bm0000889
Chan-Thaw, C. E., Villa, A., Katekomol, P., Su, D., Thomas, A., and Prati, L. (2010). Covalent triazine framework as catalytic support for liquid phase reaction. Nano Lett. 10, 537–541. doi: 10.1021/nl904082k
Chu, L., Liu, C., and Zhou, G. (2015). A double network gel as low cost and easy recycle adsorbent: highly efficient removal of Cd(II) and Pb(II) pollutants from wastewater. J. Hazard. Mater. 300, 153–160. doi: 10.1016/j.jhazmat.2015.06.070
Copello, G. J., Diaz, L. E., and Orto, V. C. D. (2012). Adsorption of Cd(II) and Pb(II) onto a one step-synthesized polyampholyte: kinetics and equilibrium studies. J. Hazard. Mater. 217–218, 374–381. doi: 10.1016/j.jhazmat.2012.03.045
Dong, J., Worthen, A. J., Foster, L. M., Chen, Y., Cornell, K. A., Bryant, S. L., et al. (2014). Modified montmorillonite clay microparticles for stable oil-in-seawater emulsions. ACS Appl. Mater. Interfaces 6, 11502–11513. doi: 10.1021/am502187t
Efome, J. E., Rana, D., Matsuura, T., and Lan, C. Q. (2018). Insight studies on metal-organic framework nanofibrous membrane adsorption and activation for heavy metal ions removal from aqueous solution. ACS Appl. Mater. Interfaces 10, 18619–18629. doi: 10.1021/acsami.8b01454
El-Bahy, S. M. (2018). New iminodiacetate chelating resin-functionalized Fe3O4 nanoparticles: synthesis, characterization, and application for the removal of some noxious metal ions from wastewater. J. Chem. Eng. Data 63, 2299–2313. doi: 10.1021/acs.jced.8b00241
Gan, Q., Shi, W., Xing, Y., and Hou, Y. (2018). A polyoxoniobate/g-C3N4 nanoporous material with high adsorption capacity of methylene blue from aqueous solution. Front. Chem. 6:7. doi: 10.3389/fchem.2018.00007
Ghorai, S., Sarkar, A., Raoufi, M., Panda, A. B., Schönherr, H., and Pal, S. (2014). Enhanced removal of methylene blue and methyl violet dyes from aqueous solution using a nanocomposite of hydrolyzed polyacrylamide grafted xanthan gum and incorporated nanosilica. ACS Appl. Mater. Interfaces 6, 4766–4777. doi: 10.1021/am4055657
Hu, Y., Gu, X., Yang, Y., Huang, J., Hu, M., Chen, W., et al. (2014). Facile fabrication of poly (l-lactic acid)-grafted hydroxyapatite/poly (lactic-co-glycolic acid) scaffolds by pickering high internal phase emulsion templates. ACS Appl. Mater. Interfaces 6, 17166–17175. doi: 10.1021/am504877h
Ikem, V. O., Menner, A., and Bismarck, A. (2010a). High-porosity macroporous polymers sythesized from titania-particle-stabilized medium and high internal phase emulsions. Langmuir 26, 8836–8841. doi: 10.1021/la9046066
Ikem, V. O., Menner, A., and Bismarck, A. (2011). Tailoring the mechanical performance of highly permeable macroporous polymers synthesized via Pickering emulsion templating. Soft Matter 7, 6571–6577. doi: 10.1039/c1sm05272a
Ikem, V. O., Menner, A., Horozov, T. S., and Bismarck, A. (2010b). Highly permeable macroporous polymers synthesized from pickering medium and high internal phase emulsion templates. Adv. Mater. 22, 3588–3592. doi: 10.1002/adma.201000729
Kou, Y., Xu, Y., Guo, Z., and Jiang, D. (2011). Supercapacitive energy storage and electric power supply using an aza-fused π-conjugated microporous framework. Angew Chem. 123, 8912–8916. doi: 10.1002/ange.201103493
Kovačič, S., AnŽlovar, A., Erjavec, B., Kapun, G., Matsko, N. B., Žigon, M., et al. (2014). Macroporous ZnO foams by high internal phase emulsion technique: synthesis and catalytic activity. ACS Appl. Mater. Interfaces 6, 19075–19081. doi: 10.1021/am5050482
Li, M., Zhang, Z., Li, R., Wang, J. J., and Ali, A. (2016). Removal of Pb(II) and Cd(II) ions from aqueous solution by thiosemicarbazide modified chitosan. Int. J. Biol. Macromol. 86, 876–884. doi: 10.1016/j.ijbiomac.2016.02.027
Liang, J., Li, X., Yu, Z., Zeng, G., Luo, Y., Jiang, L., et al. (2017). Amorphous MnO2 modified biochar derived from aerobically composted swine manure for adsorption of Pb (II) and Cd (II). ACS Sustain. Chem. Eng. 5, 5049–5058. doi: 10.1021/acssuschemeng.7b00434
Liu, R., Cho, S. I., and Lee, S. B. (2008). Poly (3, 4-ethylenedioxythiophene) nanotubes as electrode materials for a high-powered supercapacitor. Nanotechnology 19:215710. doi: 10.1088/0957-4484/19/21/215710
Luo, S., Li, X., Chen, L., Wan, Y., and Liu, C. (2014). Layer-by-layer strategy for adsorption capacity fattening of endophytic bacterial biomass for highly effective removal of heavy metals. Chem. Eng. J. 239, 312–321. doi: 10.1016/j.cej.2013.11.029
Ma, J., Li, T., Liu, Y., Cai, T., Wei, Y., Dong, W., et al. (2019). Rice husk derived double network hydrogel as efficient adsorbent for Pb(II), Cu(II) and Cd(II) removal in individual and multicomponent systems. Bioresour. Technol. 290:121793. doi: 10.1016/j.biortech.2019.121793
Madadrang, C. J., Kim, H. Y., Gao, G., Wang, N., Zhu, J., Feng, H., et al. (2012). Adsorption behavior of EDTA–graphene oxide for Pb(II) removal. ACS Appl. Mater. Interfaces 4, 1186–1193. doi: 10.1021/am201645g
Özdemir, S., Kilinç, E., Poli, V., Okumuş, V., Poli, A., Nicolaus, B., et al. (2016). Thermophilic Geobacillus galactosidasius sp. nov. loaded γ-Fe2O3 magnetic nanoparticle for the preconcentrations of Pb and Cd. Bioresour. Technol. 201, 269–275. doi: 10.1016/j.biortech.2015.11.052
Pierre, S. J., Thies, J. C., Dureault, A., Cameron, N. R., van Hest, J. C. M., Carette, N., et al. (2006). Covalent enzyme immobilization onto photopolymerized highly porous monoliths. Adv. Mater. 18, 1822–1826. doi: 10.1002/adma.200600293
Pulko, I., Wall, J., Krajnc, P., and Cameron, N. R. (2010). Ultra-high surface area functional porous polymers by emulsion templating and hypercrosslinking: efficient nucleophilic catalyst supports. Chemistry 16, 2350–2354. doi: 10.1002/chem.200903043
Venkateswarlu, S., and Yoon, M. (2015). Core–shell ferromagnetic nanorod based on amine polymer composite (Fe3O4@DAPF) for fast removal of Pb(II) from aqueous solutions. ACS Appl. Mater. Interfaces 7, 25362–25372. doi: 10.1021/acsami.5b07723
Vílchez, A., Rodríguez-Abreu, C., Esquena, J., Menner, A., and Bismarck, A. (2011). Macroporous polymers obtained in highly concentrated emulsions stabilized solely with magnetic nanoparticles. Langmuir 27, 13342–13352. doi: 10.1021/la2032576
Viswanathan, P., Johnson, D. W., Hurley, C., Cameron, N. R., and Battaglia, G. (2014). 3D surface functionalization of emulsion-templated polymeric foams. Macromolecules 47, 7091–7098. doi: 10.1021/ma500968q
Viswanathan, P., Ondeck, M. G., Chirasatitsin, S., Ngamkham, K., and Reilly, G. C. (2015). 3D surface topology guides stem cell adhesion and differentiation. Biomaterials 52, 140–147. doi: 10.1016/j.biomaterials.2015.01.034
Wang, C. P., Wu, J. Z., Sun, H. W., Wang, T., Liu, H. B., and Chang, Y. (2011). Adsorption of Pb(II) ion from aqueous solutions by tourmaline as a novel adsorbent. Ind. Eng. Chem. Res. 50, 8515–8523. doi: 10.1021/ie102520w
Wang, F., Zhu, Y., Wang, W., Zong, L., Lu, T., and Wang, A. (2017a). Fabrication of CMC-g-PAM superporous polymer monoliths via eco-friendly Pickering-MIPEs for superior adsorption of methyl violet and methylene blue. Front. Chem. 5:33. doi: 10.3389/fchem.2017.00033
Wang, J., Wei, L., Ma, Y., Li, K., Li, M., Yu, Y., et al. (2013). Collagen/cellulose hydrogel beads reconstituted from ionic liquid solution for Cu(II) adsorption. Carbohydr. Polym. 98, 736–743. doi: 10.1016/j.carbpol.2013.06.001
Wang, N., Ouyang, X. K., Yang, L. Y., and Omer, A. M. (2017b). Fabrication of a magnetic cellulose nanocrystal/metal-organic framework composite for removal of Pb(II) from water. ACS Sustain. Chem. Eng. 5, 10447–10458. doi: 10.1021/acssuschemeng.7b02472
Wang, Z. J., Ghasimi, S., Landfester, K., and Zhang, K. A. (2014). Highly porous conjugated polymers for selective oxidation of organic sulfides under visible light. Chem. Commun. 50, 8177–8180. doi: 10.1039/C4CC02861A
Wen, P., Xue, M., Ishikawa, Y., Itoh, H., and Feng, Q. (2012). Relationships between cell parameters of dye-sensitized solar cells and dye-adsorption parameters. ACS Appl. Mater. Interfaces 4, 1928–1934. doi: 10.1021/am3001693
Wong, L. L. C., Ikem, V. O., Menner, A., and Bismarck, A. (2011). Macroporous polymers with hierarchical pore structure from emulsion templates stabilised by both particles and surfactants. Macromol. Rapid Commun. 32, 1563–1568. doi: 10.1002/marc.201100382
Wu, Y., Ma, Y., Pan, J., Gu, R., and Luo, J. (2017). Porous and magnetic molecularly imprinted polymers via Pickering high internal phase emulsions polymerization for selective adsorption of λ-cyhalothrin. Front. Chem. 5:18. doi: 10.3389/fchem.2017.00018
Wu, Y., Tang, Y., Li, L., Liu, P., Li, X., Chen, W., et al. (2018). The correlation of adsorption behavior between ciprofloxacin hydrochloride and the active sites of Fe-doped MCM-41. Front. Chem. 6:17. doi: 10.3389/fchem.2018.00017
Xu, H., Zheng, X., Huang, Y., Wang, H., and Du, Q. (2015). Interconnected porous polymers with tunable pore throat size prepared via Pickering high internal phase emulsions. Langmuir 32, 38–45. doi: 10.1021/acs.langmuir.5b03037
Yang, J., Wu, J. X., Lü, Q. F., and Lin, T. T. (2014). Facile preparation of lignosulfonate–graphene oxide–polyaniline ternary nanocomposite as an effective adsorbent for Pb(II) ions. ACS Sustain. Chem. Eng. 2, 1203–1211. doi: 10.1021/sc500030v
Ye, S., Yu, H. Y., Wang, D., Zhu, J., and Gu, J. (2018). Green acid-free one-step hydrothermal ammonium persulfate oxidation of viscose fiber wastes to obtain carboxylated spherical cellulose nanocrystals for oil/water Pickering emulsion. Cellulose 25, 1–17. doi: 10.1007/s10570-018-1917-x
Yi, W., Wu, H., Wang, H., and Du, Q. (2016). Interconnectivity of macroporous hydrogels prepared via graphene oxide-stabilized pickering high internal phase emulsions. Langmuir 32, 982–990. doi: 10.1021/acs.langmuir.5b04477
Yu, S., Tan, H., Wang, J., Liu, X., and Zhou, K. (2015). High porosity supermacroporous polystyrene materials with excellent oil–water separation and gas permeability properties. ACS Appl. Mater. Interfaces 7, 6745–6753. doi: 10.1021/acsami.5b00196
Zhang, S., Chen, J., and Perchyonok, V. T. (2009). Stability of high internal phase emulsions with sole cationic surfactant and its tailoring morphology of porous polymers based on the emulsions. Polymer 50, 1723–1731. doi: 10.1016/j.polymer.2008.11.004
Zhang, S., Zhu, Y., Hua, Y., Jegat, C., Chen, J., and Taha, M. (2011). Stability of surfactant-free high internal phase emulsions and its tailoring morphology of porous polymers based on the emulsions. Polymer 52, 4881–4890. doi: 10.1016/j.polymer.2011.08.022
Zhang, Y., Wang, S., Eghtedari, M., Motamedi, M., and Kotov, N. A. (2005). Inverted-colloidal-crystal hydrogel matrices as three-dimensional cell scaffolds. Adv. Funct. Mater. 15, 725–731. doi: 10.1002/adfm.200400325
Zhang, Y., Zhao, L., Patra, P. K., and Ying, J. Y. (2008). Synthesis and catalytic applications of mesoporous polymer colloids in olefin hydrosilylation. Adv. Synth. Catal. 350, 662–666. doi: 10.1002/adsc.200700619
Zhao, C., Danish, E., Cameron, N. R., and Kataky, R. (2007). Emulsion-templated porous materials (PolyHIPEs) for selective ion and molecular recognition and transport: applications in electrochemical sensing. J. Mater. Chem. 17, 2446–2453. doi: 10.1039/b700929a
Zheng, X., Zhang, Y., Wang, H., and Du, Q. (2014). Interconnected macroporous polymers synthesized from silica particle stabilized high internal phase emulsions. Macromolecules 47, 6847–6855. doi: 10.1021/ma501253u
Zhou, Y., Fu, S., Zhang, L., Zhan, H., and Levit, M. V. (2014). Use of carboxylated cellulose nanofibrils-filled magnetic chitosan hydrogel beads as adsorbents for Pb(II). Carbohydr. Polym. 101, 75–82. doi: 10.1016/j.carbpol.2013.08.055
Zhu, Y., Wang, W., Zheng, Y., Wang, F., and Wang, A. (2016a). Rapid enrichment of rare-earth metals by carboxymethyl cellulose-based open-cellular hydrogel adsorbent from HIPEs template. Carbohydr. Polym. 140, 51–58. doi: 10.1016/j.carbpol.2015.12.003
Zhu, Y., Zhang, S., Hua, Y., Chen, J., and Hu, C. P. (2010). Hydrophilic porous polymers based on high internal phase emulsions solely stabilized by poly (urethane urea) nanoparticles. Polymer 51, 3612–3617. doi: 10.1016/j.polymer.2010.06.008
Zhu, Y., Zheng, Y., Wang, F., and Wang, A. (2016b). Fabrication of magnetic macroporous chitosan-g-poly (acrylic acid) hydrogel for removal of Cd2+ and Pb2+. Int. J. Biol. Macromol. 93(Pt A), 483–492. doi: 10.1016/j.ijbiomac.2016.09.005
Zhu, Y., Zheng, Y., Wang, F., and Wang, A. (2016c). Monolithic supermacroporous hydrogel prepared from high internal phase emulsions (HIPEs) for fast removal of Cu2+ and Pb2+. Chem. Eng. J. 284, 422–430. doi: 10.1016/j.cej.2015.08.157
Zou, S., Liu, H., Yang, Y., Wei, Z., and Wang, C. (2013a). Multihollow nanocomposite microspheres with tunable pore structures by templating Pickering double emulsions. React. Funct. Polym. 73, 1231–1241. doi: 10.1016/j.reactfunctpolym.2013.06.006
Keywords: macroporous materials, Pickering emulsions, montmorillonite, adsorption, heavy metal
Citation: Wang F, Zhu Y, Xu H and Wang A (2019) Preparation of Carboxymethyl Cellulose-Based Macroporous Adsorbent by Eco-Friendly Pickering-MIPEs Template for Fast Removal of Pb2+ and Cd2+. Front. Chem. 7:603. doi: 10.3389/fchem.2019.00603
Received: 30 May 2019; Accepted: 16 August 2019;
Published: 10 September 2019.
Edited by:Maria Graca Rasteiro, University of Coimbra, Portugal
Reviewed by:Tianyi Ma, University of Newcastle, Australia
Federica Valentini, University of Rome Tor Vergata, Italy
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*Correspondence: Aiqin Wang, email@example.com