Preparation, characterization and application of CS@PDA@Fe3O4 nanocomposite as a new magnetic nano-adsorber for the removal of metals and dyes in wastewater.

This study aimed to develop a novel magnetic chitosan/dopamine/Fe3O4 nano-adsorber (CS@PDA@Fe3O4) for the removal of heavy metal ions and organic dye molecules from aqueous solution. CS@PDA@Fe3O4 was prepared by surface modification of PDA/Fe3O4 nanoparticles with chitosan using IPTES as the cross-linker. The surface structure, composition, and properties of the CS@PDA@Fe3O4 nano-adsorber were characterized by elemental (EDS), spectroscopic (XRD, XPS, and FT-IR), magnetic intensity (VSM), surface and morphological (TEM and SEM) analyses. In order to study its adsorption behavior, equilibrium and kinetics studies were carried out through batch experiments. Additionally, the influences of the pH value, initial concentration, adsorbent dose, and contact time were also evaluated. The CS@PDA@Fe3O4 nano-adsorber exhibited high adsorption capacity especially for Cu(ii), with a maximum adsorption capacity of 419.6 mg g-1. The experimental data were well described by the Langmuir isotherm kinetic models. This journal is © The Royal Society of Chemistry.

Introduction

A growing social and economic concern is water contamination due to the discharge of many dyes and heavy metal ions into the environment, which causes a potential threat to human health and the environment.[1,2] As everyone knows, heavy metal ions and most of the dyes are very poisonous or strongly oncogenic, and may cause bad effects to people's brains, lungs, and kidneys.[3] Therefore, it is particularly important to treat wastewater with a feasible and appropriate method.[4] The traditional ways such as electrochemical precipitation,[5] sorption,[6] reduction,[7] advanced oxidation,[8]etc. have been used to remove pollutants from water. In all technologies, the adsorption method has the advantages of low cost, and being green and environmentally friendly for the elimination of pollutants in water.[9] Various adsorbents have been reported for the treatment of metal ions and dye-contaminated water: activated carbon, zeolites, and clay minerals, which have disadvantages such as low adsorption abilities, narrow application scope, and difficult recovery problem.[10] New materials modified by natural adsorbents for easy adsorbent recovery have received extensive attention in recent years.[11]

Chitosan (CS), as the second most abundant natural polysaccharide after cellulose, has a large number of hydroxyl and amino functional groups in its chain moiety and exerts outstanding ability to interact with a wide variety of molecules by physical and chemical forces.[12] Therefore, it can be used for wastewater treatment.[13-15] However, the solubility of chitosan in an acidic environment limits its further application.[16] Due to using glutaraldehyde as a crosslinking agent in the traditional method, the amino content of chitosan decreased sharply, which affected the adsorption property. Therefore, we introduce dopamine as a new cross-linking agent for surface modification or modification.[17,18]

Dopamine (DA), a protein-based biomaterial that is found in the tentacles of mussel sea creatures, has abundant functional groups such as catechol groups, amine groups, and aromatic moieties. Hence, it can easily adsorpt heavy metal ions and toxic organic pollutants through chelation and π–π stacking interactions.[19,20] Furthermore, it has some advantages of easy processing, in a one-pot preparation method and chemical versatility, which proved to be a powerful tool for the removal of environmental water pollutants.[21,22]

In this study, a new, low-cost, nano-adsorber with the increased number of adsorption sites was developed. This new biopolymer adsorbent is a chitosan derivative, CS@PDA@Fe3O4 which was synthesized by assembling biomimetic polymer (PDA) and chitosan onto magnetic nanoparticles based on esterification reaction. The structure and properties of nano-adsorber were investigated by means of FTIR, SEM, TEM, XRD, VSM, and elemental analysis. The various studies in terms of isotherms and kinetics of adsorption of heavy metal ions and organic dye molecules were carried out. The effects of solution pH, dosage, initial concentration, and contact time on the adsorption process were optimized.

Experimental

Instruments and materials

FeCl2·4H2O, FeCl3·6H2O, sodium hydroxide (NaOH) and dopamine (DA) were purchased from Kaixin Chemical Industry. Trometamol was purchased from Zhongqin Chemical Reagent (Shanghai, China). Chitosan and γ-isocyanatopropyltriethoxysilane (IPTES) were purchased from Odofuni Biological Technology (Nanjing, China). Hydrochloric acid (HCl) was purchased from Chemical Factory (Beijing, China). Methylene blue (MB), Fuchsin basic (FB), Rhodamine B (RhB) were cationic dyes gained from Damao Chemical Reagent Factory (Tianjin, China). All other reagents were analytical grade and were used without any extra purification. Aqueous solutions at various concentrations were prepared from HgCl2, were used as sources for Hg(ii), CuCl2, PbCl2 were used as sources for Cu(ii), Pb(ii), respectively. The morphology was analyzed by scanning electron microscopy (SEM) (MIRN3, TESCAN, China) and (TEM) (Philip Tecnai20, Netherlands). Infrared spectroscopy was recorded by a Fourier transform infrared spectrometer (FTIR) (Vector22, Bruker, Germany). Vibrating-sample magnetometry (VSM) (Lake Shore7410, America). The types and contents of the elements were analyzed by an energy dispersive spectrometer (EDS) (FE SEM-4100, Hitachi Limited, Japan).

Synthesis of magnetite Fe3O4 nanoparticles

Magnetite Fe3O4 nanoparticles were synthesized by the method of coprecipitation according to reported investigation.[23] Briefly, FeCl3 (8.15 g) and FeCl2 (3.98 g) were weighed and dissolved in 25 mL deionized water respectively, the obtained mixture was mixed further stirred for 30 min at 60 °C, followed by NaOH (100 mL, 2 mol L−1) for another 2 h. The produced mixture was washed in deionized water until neutral and dried at 70 °C for 12 h to obtain Fe3O4 nanoparticles.

Preparation of PDA@Fe3O4 nanocomposite

In a round-bottom flask, a solution of 300 mL of Tris–HCl buffer solution (pH = 8.5) was configured and then a certain amount of dopamine and magnetic Fe3O4 nanoparticles (1 g) was added. After sonication for 30 min, the reaction temperature was rose to 100 °C for 12 h to obtain the PDA@Fe3O4 nanocomposite.

Synthesis of CS@PDA@Fe3O4 nanocomposite

Chitosan (0.5 g) was added to anhydrous pyridine solution at 90 °C for 12 h. Add 0.5 mL IPTES in constant temperature stirring for 12 h. Then, PDA@Fe3O4 (0.5 g) was added, the stirring of mixture continued for 12 h. The black CS@PDA@Fe3O4 nanocomposite was separated using the magnetic decantation, washed with distilled water and alcohol thoroughly. The product was dried at 70 °C under the vacuum for 12 h.

Adsorption experiments

The adsorption was studied by batch methods that were carried out by placing CS@PDA@Fe3O4 (0.01 g) in series of flasks containing heavy metal ions or dyes in an aqueous solution (30 mL) with the desired initial concentration and pH. Then, the flasks were shaken in a thermostat oscillator at a certain temperature with the constant rate for a given time. The effects of operating variables such as pH value, contact time, initial concentration, and amount of adsorbent on the degree of adsorption were investigated. To investigate the effect of different solution pH on adsorption of heavy metal and dye, the desired pH range of the heavy metal and dye was adjusted from 1 to 7. The working concentration of heavy metal ions or dyes was 5.4 g L−1 for kinetic studies and 1.35–8.1 g L−1 for isotherm studies. Separate the magnetic microsphere CS@PDA@Fe3O4 from the solution and measure the absorbance of the solution before and after adsorption.

The amount of pollutant adsorbed per gram of the adsorber was calculated based on the following equation.[24]where η is the adsorption capacity (mg g−1); C0 and Ce are initial and equilibrium concentrations of the heavy metal ions or dyes (mg L−1) in the testing solution (mg L−1); V is the volume of the solution (L), and M is the weight of resin beads (g).

Recycling of CS@PDA@Fe3O4 nanocomposite

For the desorption experiment, the CS@PDA@Fe3O4 nanocomposite was separated, washed several times with absolute ethanol solution and distilled water, and used for the subsequent adsorption after drying at 70 °C under the vacuum for 12 h. In order to test the reusability of the CS@PDA@Fe3O4 nanocomposite, this adsorption–desorption cycle was repeated 6 times by using the same adsorbent.

Results and discussion

Characterization of CS@PDA@Fe3O4 biopolymer adsorbent

The nanoparticles of CS@PDA@Fe3O4 were synthesized in a three-step procedure. The CS@PDA@Fe3O4 was prepared using coating layer upon layer of Fe3O4, PDA and CS (Fig. 1). The adsorption principle of CS@PDA@Fe3O4 biopolymer adsorbent was that its chitosan layer molecule contains a large number of amino and hydroxyl groups, which formed mesh cage molecules by hydrogen bond, chelate many heavy metal ions and dye molecules. The prepared CS@PDA@Fe3O4 nanocomposite was characterized by various techniques such as FT-IR, vibration sample magnetometer (VSM), X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscope (SEM), energy dispersive X-ray spectrometer (EDS), and X-ray photoelectron spectroscopy (XPS) analyses.

Fig. 1

Synthesis of CS@PDA@Fe3O4 nanocomposite and heavy metal ion absorption.

TEM, SEM, VSM, FT-IR and XRD of CS@PDA@Fe3O4

The FT-IR spectra of Fe3O4, PDA@Fe3O4 and CS@PDA@Fe3O4 were shown in Fig. S1.† The peaks at 585 cm−1 and 623 cm−1 in these three spectra are attributed to the Fe3O4 characteristic absorption. In the spectrum of PDA@Fe3O4, the peaks at 1610 cm−1 could be attributed to the vibrations of the aromatic ring in PDA, which is consistent with the reference reported.[22] In CS@PDA@Fe3O4, the peaks absorption at 2914 cm−1 and 3453 cm−1 correspond to –OH stretching vibrations and –NH2 stretching vibrations, respectively. Compared with the pure Fe3O4, the new peak at 1097 cm−1 is attributed to Si–O stretching vibrations of the crosslinking agent IPTES, and all results indicate that CS@PDA@Fe3O4 nano-adsorber has been successfully synthesized.

The magnetic hysteresis loops of Fe3O4, PDA@Fe3O4 and CS@PDA@Fe3O4, at 300 K, are shown in Fig. 1b. The magnetization saturation (MS) value of the above materials was 80.5, 68.5 and 38.2 emu g−1, respectively. Although the magnetic intensity decreases obviously after the coating of dopamine and chitosan layer by layer, the CS@PDA@Fe3O4 nano-adsorber can still be easily separated by using magnetic field, and facilitated collection, regeneration, and reutilization (shown in the insets in Fig. S2†).[25]

The XRD patterns of Fe3O4, PDA@Fe3O4, CS@PDA@Fe3O4 are displayed in Fig. S3.† The six peaks of Fe3O4 at 2θ = 30.5°, 35.6°, 43.2°, 54°, 57.4°, and 62.9° highly match the characteristic peaks of magnetite (Fe3O4, PDF NO. 01-071-6336).[26] There is no obvious characteristic peak of dopamine in PDA@Fe3O4, indicating that the structure of dopamine coating Fe3O4 is amorphous. In the spectrum of CS@PDA@Fe3O4, an obvious crystal characteristic diffraction peaks at 2θ = 20.6°, which belongs to the characteristic crystal peak of chitosan, further proving the successful introduction with chitosan to the surface of Fe3O4 nanoparticle. Moreover, the diffraction peaks of Fe3O4 crystal are well consistent with the characteristic diffraction peaks of CS@PDA@Fe3O4. These results indicated the Fe3O4 was successfully introduced. The surface morphologies of the pure Fe3O4 and the CS@PDA@Fe3O4 were shown in Fig. S4.† By comparing Fig. S4d and e,† it could be clearly observed that the surfaces of the CS@PDA@Fe3O4 (Fig. S4e†) are smoother and the volume increased significantly than Fe3O4 (Fig. S4d†). They remained basically consistent, which were spherically granular and partially barreled. It can be seen from Fig. 1c and d that the agglomeration phenomenon of CS@PDA@Fe3O4 (Fig. S4g†) is much weaker than Fe3O4 (Fig. S4f†) due to the surface modification by coated of the chitosan. Thus, it proved that Fe3O4 as a magnetic core was coated.

EDS of CS@PDA@Fe3O4

We also compared the proportion of N, C, H, Fe, Si in Fe3O4, PDA@Fe3O4 and CS@PDA@Fe3O4 performed with EDS data, the results were listed in Table S1.† The significant improvement of N and C element content about PDA@Fe3O4 strongly demonstrated the successful introduction of dopamine, formed a coating layer on Fe3O4. The Si content in CS@PDA@Fe3O4 was provided by linker IPTES in the synthesis process, thus it can be seen that CS@PDA@Fe3O4 nano-adsorber was successfully synthesized.

Adsorption mechanism of the CS@PDA@Fe3O4 nano-adsorber

The XPS analysis was further carried out to study the chemical elements on the surface of the nano-adsorber and the adsorption mechanism of nano-adsorber on heavy metal ions and dye molecules. Taking the adsorption of Cu(ii) as an example, virgin and Cu(ii)-loaded CS@PDA@Fe3O4 was performed. The wide scan spectra of the CS@PDA@Fe3O4 before and after Cu(ii) adsorption showed the same peak components of C, N, O, Fe, and Si elements (Fig. S5a†). After adsorption, new peaks appear at 931 and 74 eV, which can be attributed to Cu 2p and Cu 3p, the peak of Cl 3p at 200 eV. Based on the comparison and analysis, it is reasonable to believe that the Cu(ii) was loaded onto the nano-adsorber.

By comprising the N 1s spectrum of the virgin and Cu(ii)-loaded CS@PDA@Fe3O4 in Fig. S5b,† the peak for the species of –NH2 (396.6 eV) was increased to 396.8 eV and the peak of –NH– (397.1 eV) increased to 398.1 eV after Cu(ii) adsorption.[27] Fig. S5c† shows the O 1s spectrum of PDA/CS/Fe3O4 before and after adsorption. After Cu(ii) adsorption, the peak for the species of –OH (527.1 eV) was increased to 527.3 eV and the peak of C–O (397.1 eV) increased to 529.5 eV after Cu(ii) adsorption. It is further demonstrated that the amino group and hydroxyl group play an important role in the adsorption process of CS@PDA@Fe3O4.[28]

Effect of contact time, pH, adsorbent dose and initial concentration on properties of the CS@PDA@Fe3O4 nano-adsorber

The effect of contact time for the adsorption of heavy metals ions and organic dyes molecules by CS@PDA@Fe3O4 nano-adsorber at various intervals of time ranging from 10 to 120 min was investigated in the ambient experimental background. The results obtained were presented in Fig. 2a. The results confirmed that adsorption of metal ions and dyes has a consistent change rule: the initial stage of the rate of adsorption was faster and then gradually reduced and reached saturation.[13] Thus, 30 min, 70 min, 80 min, 100 min, 60 min, 60 min of contact time were respectively optimized for the adsorptive removal of Cu(ii), Hg(ii), Pb(ii), MB, FB and RhB.

Fig. 2

Effect of (a) shacking time; (b) initial pH and (c) adsorbent dosage on the adsorption with the pH value of the solution was 7 at ambient experimental conditions.

The solution pH, as a critical operational variable, has a significant effect on the surface charge of the adsorption and the metal ion chemistry. For that, we investigated different processes when the pH ranged from 1 to 12 for heavy metal ions and dyes. The Cu(ii) cations tend to precipitate in the form of hydroxyl salts of Cu(ii) ions and FB has a large color change in alkaline solution, which has a detrimental effect on adsorption research. Therefore, the pH range of both of them was adjusted to 1–7. It can be seen from Fig. 2b that the removal rate of adsorbent on metal ions and dye molecules increases gradually with the increasing pH of the solution under acidic conditions. When the solution was neutral, the adsorption reaches saturation. The strongly acidic and alkaline conditions are not conducive to the effect of metal ions and dyes. The strong acidic solution containing a large number of H+ will form a competitive relationship with metal ions for adsorption reduce the active sites, and there will be the partial dissolution of chitosan, thus reducing the adsorption performance. Besides, metal ions may be partially precipitated under basic conditions. In consequence, the optimum pH of heavy metal ions and dye molecules adsorption onto CS@PDA@Fe3O4 nano-adsorber was 7.

The adsorbent dosage is a key parameter for the sorption capacity of adsorbents. The dosage of CS@PDA@Fe3O4 nano-adsorber was varied in the range of 40–240 mg, in a fixed initial dyes and heavy metal ions concentration of 50 mg L−1, the pH value of the solution was 7, at ambient experimental conditions. The effect of the adsorbent dosage on the adsorption of heavy metal ions and dye molecules were investigated, and the results were shown in Fig. 2c. With the increase of adsorption dose, the adsorption efficiency of heavy metal ions and dye molecules increased, which could be described based on the availability of active binding sites for the adsorbates on the surface of the adsorbent. When the amount of adsorbent increases to a certain value, the removal rate decreases after it remains stable. The reason could be that after the adsorption reaches equilibrium, part of the adsorbent will fall off from the adsorbent. Therefore, 100 mg of the CS@PDA@Fe3O4 nano-adsorber was chosen as the ideal dose for the following adsorption experiment.

The effects of different initial concentrations of dye molecules and heavy metal ions on their adsorption at optimal contact time and pH were investigated. The relationship between adsorption amount and initial concentration was presented in Fig. 3. The adsorption of heavy metal ions and dye molecules showed a common change rule. As the initial concentration increases, the collision probability between the magnetic microspheres and the adsorbent increases, but when the initial concentration is large enough, the adsorption sites of the nano-adsorber are filled and saturated, and the removal rate reaches equilibrium or even decreases.

Fig. 3

Effect of initial concentration on adsorption at 30 °C.

Adsorption kinetics

The adsorption kinetics are the crucial factors for determining the rate of the adsorption process, which provides essential data about the mechanism and rate of removal. Table 1 shows the kinetic profiles of heavy metals ions and organic dyes adsorption operation using CS@PDA@Fe3O4 as adsorbents, with time increasing. In order to investigate the removal mechanism of the adsorption of Cu(ii), Hg(ii), Pb(ii) heavy metal ions and MB, FB, RhB dye molecules on CS@PDA@Fe3O4 nano-adsorber, the pseudo-first-order (3), pseudo-second-order (4) and intraparticle diffusion kinetic models (5) were employed to explore the experimental data.[29]where K1, K2 and Kint are pseudo-first-order rate constant (min−1), pseudo-second-order rate constant (g mg−1 min−1) and intraparticle diffusion rate constant (mg g−1 min−1/2) of adsorption, respectively. Q and Q are the adsorption capacity (mg g−1) at equilibrium time and at time t (min), respectively. C (mg g−1) is a constant of the intra-particle diffusion model.

Parameters of kinetics model for adsorption of pollutants on CS@PDA@Fe3O4

Pollutants	Pseudo-first-order			Pseudo-second-order			Intraparticle diffusion
	Q	K 1	R 2	Q	K 2	R 2	K int	R 2
Cu2+	784.15	0.145	0.8746	416.67	0.0032	0.9999	57.404	0.9255
Hg2+	9.16	0.032	0.9622	42.90	0.0035	1.0000	0.2349	0.9758
Pb2+	2.63	0.048	0.8657	12.48	0.0400	0.9999	0.1563	0.9909
MB	2.07	0.061	0.6893	2.99	0.1020	0.9993	0.0464	0.986
FB	1.24	0.043	0.9626	2.48	0.0550	0.9974	0.0789	0.9091
RhB	0.58	0.055	0.9130	3.08	0.1500	0.9997	0.0149	0.9531

The non-linear form of the reaction and diffusion-based kinetic parameters and their results were summarized in Table 1. Through the comparison and analysis of R2 values in the table, the kinetic model. With the higher R2 values of the pseudo-second-order kinetics model, the conclusion is drawn that the pseudo-second-order kinetics model was well simulated, which signifying that chemisorption dominated the adsorption process.

Adsorption isotherms

The adsorption isotherms are the crucial factors for optimizing the application of absorbent, which explain the interaction between adsorbate molecules and adsorbent.

For the adsorption isotherm studies, the adsorption data of heavy metal ions and dye molecules were fitted to Langmuir (6) and Freundlich (7) equations, respectively.[30] The results were shown in Table 2.where Ce is the equilibrium concentration of metal ions in solution (mg L−1), and Q is the equilibrium adsorption capacity (mg g−1), Qmax (mg g−1) and KL (L mg−1) are the Langmuir constant which is related to the adsorption capacity and energy of adsorption, respectively. Kf is the Freundlich constant related to adsorption capacity.

Parameters of isotherm model for adsorption of pollutants on CS@PDA@Fe3O4

Pollutants	Langmuir parameters			Freundlich parameters
	K L	Q max	R 2	ln Kf	N	R 2
Cu(ii)	22.0	909.0	0.9759	9.2199	1.015	0.9713
Hg(ii)	35.4	94.0	0.9868	5.246	2.70	0.9883
Pb(ii)	165.0	20.2	0.9955	3.4434	5.50	0.9490
MB	0.4	3.6	0.9833	0.0565	2.416	0.9267
FB	12.3	2.4	0.9905	0.3238	5.214	0.9501
RhB	13.1	2.9	0.9287	0.4508	3.948	0.9465

The R2 of both fitting models is relatively high, and the R2 of the Langmuir model is generally higher than that of the Freundlich model. This result indicates that the adsorption of pollutants on PDA/CS/Fe3O4 nano-sorbents occurred as a single monolayer, and the interaction force between metal ions can be ignored. Based on the theoretical analysis of the obtained data, the theoretical Qmax value of the nano adsorbent for Cu(ii), Hg(ii), Pb(ii), MB, FB and RhB were respectively 909.0 mg g−1, 94.0 mg g−1, 20.2 mg g−1, 3.6 mg g−1, 2.4 mg g−1, 2.9 mg g−1, which was very close to the experimental data.

Desorption and reusability

Considering the cost in practical applications, it is necessary to study the analysis and regeneration of nano-adsorber. Desorption tests were studied to assess the regeneration and recycling of the CS@PDA@Fe3O4 nanocomposite regarding removing heavy metal ions and dye molecules via performing six adsorption/desorption cycles. It can be seen from Fig. 4 that the removal rate of nano-adsorber decreased slightly after the analysis operation with an ethanol solution, but it still has high removal efficiency.

Fig. 4

Desorption and reusability of CS@PDA@Fe3O4.

Conclusions

In this paper, a simple method is used to synthesize chitosan-grafted CS@PDA@Fe3O4 magnetic nano-adsorber with Fe3O4 as the magnetic core and PDA as the intermediate layer. These nano-adsorber membranes were utilized to eliminate the heavy metal ions (Cu(ii), Hg(ii), Pb(ii)) and dye molecules (MB, FB, RhB) from aqueous solutions. The effects of static adsorption parameters such as pH, adsorbent concentration, metal initial concentration and time on adsorption performance were investigated. The results showed that the magnetic nano-adsorber had good adsorption performance and magnetic responsiveness. Besides, the experiment of desorption and regeneration proves that CS@PDA@Fe3O4 magnetic nano-adsorber can be recycled. This study has practical guiding significance for the treatment of pollutants in adsorbed water.

Conflicts of interest

There are no conflicts to declare.