Decolorization of RhB dye by manganese oxides: effect of crystal type and solution pH
© Cui et al. 2015
Received: 1 December 2014
Accepted: 29 June 2015
Published: 25 July 2015
Organic dye pollution in water has become a major source of environmental pollution. Mn(III/IV) oxides have attracted a great deal of attention to remove organic dye pollutants due to their unique structures and physicochemical properties. Numerous studies have reported the removal of dye by various Mn(III/IV) oxides through catalytic degradation and adsorption. The crystalline structures of manganese oxides and solution pH may exert substantial impact on the removal of dyes. However, few studies have focused on the oxidative degradation of RhB dye using Mn(III/IV) oxides with different crystal structures during a spontaneous reaction. In the present study, three manganese oxides with different crystal type (α-MnO2, β-MnO2, and δ-MnO2) were prepared by refluxing process to decolorize RhB dye in various pH solutions.
The results showed that the decolorization efficiencies of RhB for the three manganese oxides all increase with decrease solution pH. α-MnO2 exhibited highest activity and could efficiently degrade RhB at pH 2–6. The degradation of RhB by β-MnO2 and δ-MnO2 could be observed at pH 2–3, and only little adsorption RhB on manganese oxides could be found at pH 4–6. The UPLC/MS analysis suggests that the decolorization of RhB by manganese oxides consists of three main stages: (1) cleavage of the ethyl groups from RhB molecular to form Rh; (2) further destruction of –COOH and –CNH2 from Rh to form the small molecular substances; (3) mineralization of the small molecular substances into CO2, H2O, NO3 − and NH4 +.
Overall, these results indicate that α-MnO2 may be envisaged as efficient oxidants for the treatment of organic dye-containing wastewater under acid conditions.
In the recent years, Mn(III/IV) oxides have attracted a great deal of attention to remove organic dye pollutants due to their unique structures and physicochemical properties [5–7]. The removal efficiencies of the dye pollutants by Mn(III/IV) oxides are dependent upon their crystallographic forms, which could display layered or tunnel structures through different arrangements of MnO6 octahedra [8, 9]. Up to now, numerous studies have reported the removal of dye by various Mn(III/IV) oxides through catalytic degradation and adsorption [5, 10–12]. Few studies have focused on the oxidative degradation of RhB using Mn(III/IV) oxides with different crystal structures during a spontaneous reaction. Moreover, as reported in the previous literatures, the Mn(III/IV) oxides were commonly prepared by different methods including refluxing process, hydrothermal method, and calcination method [12–14]. The Mn(III/IV) oxides prepared using different methods often display different reactivity.
In the present work, three Mn(III/IV) manganese oxides (α-MnO2, β-MnO2, and δ-MnO2) with different crystal structures were prepared by similar refluxing process, and the products were used to decolorize RhB in various pH solutions to investigate the effects of crystal type of manganese oxides and solution pH on the removal efficiencies and mechanisms of RhB dye from waters.
Results and discussion
Characterizations of the synthetic manganese oxides
Selected properties of the synthetic manganese oxides
BET surface area (m2/g)
Decolorization of RhB dye by the manganese oxides at various pH values
UV–vis absorption spectra of the RhB solution treated with the three manganese oxides are shown in Additional file 1: Figure S2. For α-MnO2, the intensity of the RhB peaks decreased sharply within 5–10 min, and the peak of 554 nm obviously shifted to 500 nm, which indicates that the decolorization of RhB by α-MnO2 is mainly attributed to the decomposition reaction at pH 2–6 [15, 16]. Meanwhile, the same blue shift of 554 nm peak was observed at low pHs for δ-MnO2 (pH 2 and 3) and β-MnO2 (pH 2). However, only a weak decrease of the intensity of the RhB peaks, and no peak shifts were found at pH 4 and pH 6. These results implied that the decomposition reaction only occurs at pH ≤ 3 and adsorption is responsible to the decolorization of the RhB at pH > 3. Therefore, the decolorization mechanism of RhB by manganese oxides depends on the crystal type of the oxides and the solution pH.
In this investigation, the three crystallographic MnO2 showed different activities for RhB degradation, which can be related to the variation in crystalline structure, AOS, BET surface area and other physicochemical properties. At low pHs, the crystal stability of the layered structure of δ-MnO2 is weaker than that of the tunnel structures of α-MnO2 and β-MnO2, which is beneficial to the redox reaction between Mn(VI/III) and RhB. This may account for its faster oxidization of RhB at pH 2 than α-MnO2 and β-MnO2. With increasing solution pH to 4, the adsorption became fully responsive to the decolorization of RhB for δ-MnO2. However, the oxidation of RhB still could be found for α-MnO2 and β-MnO2 at pH 4. This may result in their higher decolorization rates. Compared with tunnel structure of α-MnO2 and β-MnO2, two-tunnel structured α-MnO2 showed higher activity than the single-tunnel structured β-MnO2 due to the more exposure of MnO6 edges , although the β-MnO2 has a higher AOS (3.96). Moreover, the BET surface area of β-MnO2 is much smaller than that of α-MnO2 and δ-MnO2, which means higher crystallization degree for β-MnO2. Thus, the activation energy to break the crystal structure is more than that of α-MnO2 and δ-MnO2 during redox reactions. This may explain the lower oxidation capability of β-MnO2 for RhB at low pH solution.
The variation of the solution pH influenced the surface charge properties of the dye and the manganese oxides as well as their interactions. As shown in Scheme 1, the molecular of RhB contains carboxylic group and amino group. The carboxylic group exists in the protonated state by decreasing the solution pH beyond the pKS2 value, which corresponds to 3.22, and the amino group is protonated only under very weakly basic conditions with the pKB value being 13.75 . At pH ≤ 3.22, the positively charged lead manganese oxides surface interacts more attractively with the uncharged carboxylic acid than with the positively charged amino group. At pH > PZCs of manganese oxides, the attractive interaction is established between the positively amino group and the negatively charged surface of manganese oxides. In our experiments, the decolorization efficiencies of RhB for the three manganese oxides all increased with decrease solution pH, which could be attributed to the increase of the redox potential, electron transfer, and the surface charge density of MnO2 at lower pH values. Thus, the oxidation rate of RhB by the manganese oxides is dependent upon their physicochemical parameters, crystal structures, and solution pHs.
Reduction and dissolution of the synthetic manganese oxides by RhB dye
Degradation mechanism of RhB by manganese oxides
To explore the mechanisms of the pH and crystal type on the RhB removal using manganese oxides, the intermediates of the reaction were analyzed using UPLC/MS technique. It is found that five peaks were observed at 3.05, 4.21, 4.70, 5.68, and 6.99 min in the UPLC/MS spectrum, which respectively correspond to the m/z = 331, 359, 387, 443, and 258. The signal at m/z = 443 could assign to the RhB parent ion . The peaks at m/z = 387, 359, and 331 could refer to the formation of N-ehyl-N′-ethyl-rhodamine 110 (MMRh), N-ethyl-rhodamine 110 (MRh) and rhodamine 110 (Rh) intermediates, which predicted by the cleavage of two, three, and four ethyl group from RhB molecule, respectively [21–24]. The appearance of a peak at m/z = 258 could be due to cleavage of –COOH and –CNH2 from Rh (m/z = 331). Additionally, the TOC concentration of the solution decreased from 18.2 mg/L of the initial solution to 2.3 mg/L of treatment for α-MnO2 at pH 2. Moreover, NO3 − and NH4 + could be detected in the treated solutions and the concentrations of them are 0.86 and 0.23 mg/L, respectively. These results indicated that most of the RhB could be degraded completely by manganese oxides. Based on the above experimental observations, a plausible degradation mechanism of RhB was proposed (Additional file 1: Figure S6). It is suggested that the decolorization of RhB by manganese oxides consists of three main stages: (1) cleavage of the ethyl groups from RhB molecular to form Rh; (2) further destruction of –COOH and –CNH2 from Rh to form the small molecular substances; (3) mineralization of the small molecular substances into CO2, H2O, NO3 − and NH4 +.
Three manganese oxides with different crystal type were prepared using reflux method to decolorize RhB in different pH solutions. The decolorization efficiencies of RhB for the three manganese oxides all increase with decrease solution pH. α-MnO2 presented in needles and showed the highest activity for RhB degradation at pH 2–6. δ-MnO2 and β-MnO2 had microsphere and rod-like form, respectively. These two manganese oxides showed activity to degrade RhB at pH 2–3 and only exhibited a very low adsorption rate and adsorption capacity at pH 4–6. The redox reaction between manganese oxides and RhB result in dissolution of manganese oxides and release of Mn(II). The degradation of RhB by manganese oxides consists of three main stages: (1) cleavage of the ethyl groups from RhB molecular to form Rh; (2) further destruction of –COOH and –CNH2 from Rh to form the small molecular substances; (3) mineralization of the small molecular substances into CO2, H2O, NO3 − and NH4 +. These results indicate that manganese oxides especially α-MnO2 may have potential applications in degradation of dye pollutants.
Preparation of the manganese oxides
Cryptomelane (α-MnO2) was prepared through oxidation of Mn(II) by permanganate under refluxing condition . Typically, 5.89 g of KMnO4 was dissolved in 100 mL of water and heated to boil, then a solution containing 8.8 g of MnSO4·H2O and 3 mL of concentrated HNO3 was added to the boiling solution. The mixture solution was refluxed for 24 h. The product was filtered, washed seven times with deionized water, and dried at 60°C for 24 h.
Pyrolusite (β-MnO2) was synthesized by refluxing process as reported in our previous work . In a typical procedure, a mixture of 135 mL MnSO4 solution (1.75 mol/L) and 13.6 mL concentrated HNO3 (16 mol/L) was added quickly to 450 mL of boiled KMnO4 solution (0.04 mol/L). The resultant dark brown slurry was refluxed for 36 h, then filtered and washed with deionized water several times until the pH reached ~7.0. The final products were dried in an oven at 60°C for 24 h.
Birnessite (δ-MnO2) was prepared by refluxing treatment of KMnO4 and HCl mixture solution . In a typical synthesis, 45 mL of 6 mol/L HCl was added to 400 mL of boiled KMnO4 solution (0.4 mol/L) at the rate of 0.7 L/min. The resultant dark brown slurry was refluxed for further 30 min. After being aged at 60°C for 12 h, the product was filtered, washed seven times with deionized water, and dried at 60°C for 24 h.
Characterization of the prepared manganese oxides
X-ray powder diffraction (XRD) was carried out using a Bruker D8 ADVANCE X-ray diffractometer equipped with monochromated Cu Kα radiation (λ = 0.1541 nm) at a tube voltage of 40 kV and a tube current of 40 mA. Scanning electron microscopy (SEM) images were obtained with a Hitachi S-4800 emission scanning electron microscope. ASAP 2020 M+C instrument was used to measure the superficial area and micropore size distributions of the materials. Samples were degassed in a vacuum at 250°C for about 10 h to remove water and other physically adsorbed species. The N2 isothermal adsorption and desorption experiments were performed at relative pressures (P/P0) from 10−6 to 0.9916 and from 0.9916 to 0.047, respectively. The ζ-potential of manganese oxides were measured with an MALVERN ZEN 3600 electrophoretic light scattering spectrophotometer. The three manganese oxides dispersed into deionized water to form 0.5 g/L suspension solution and then treat it with ultrasonic for 60 min. Three suspension solutions were prefiltered through a 0.45 μm pore mill filter. The values of ζ-potential under different pH were measured.
The AOS of the three manganese oxide were measured by the oxalic acid-permanganate back-titration method. Briefly, 0.1 g of the samples were completely dissolved in 10 mL of 0.5 M H2C2O4 and 10 mL of 0.5 M H2SO4 to reduce all of the manganese to Mn2+. The extra C2O4 2− was determined by back-titration at 60°C with standardized 0.02 M KMnO4 solution. The AOS was calculated on the basis of both the titration result and the total amount of Mn determined by atomic absorption spectrophotometer (AAS) .
Decolorization of RhB dye by the manganese oxides at various pH
The concentration of RhB solution was 10 mg/L, and the dosage of manganese oxides is 0.5 g/L. The solution pH was adjusted to set value by HCl and NaOH. The mixture was allowed to react in room temperature with continuous stirring. At given time intervals, an appropriate amount of suspension was taken out and quickly diluted the density to the point with distilled water. For optical absorption measurements, the diluted solution was immediately centrifuged at 12,000 rpm for 10 min to remove the manganese oxide particles. The changes of absorptions at 554 nm were applied to identify the concentrations of RhB, using a Shimadzu UV-2450 UV–vis spectrophotometer. The released of Mn(II) in the solutions were analyzed by AAS.
RhB and the intermediates generated in the degradation process were analyzed with ultra performance liquid chromatography (UPLC) triple quadrupole mass spectrometry (TQMS). Chromatographic separation was performed on a Waters Acquity UPLC system with a Crestpak C18S column that was placed at 40°C. The mobile phase was methanol/ultra pure water (1:1, v/v) at a flow rate of 0.5 mL/min. The sample injection volume was 10 μL. Mass spectrometry analysis was conducted on a Waters Aquity TQ Detector with electro spray ionization (ESI). The total organic carbon concentration in solution was analyzed using TOC analyzer (Shimadzu, TOC-vwp).
HJC and HZH carried out most of the analyses, interpreted the results and drafted the manuscript. BY and MLF designed the experiments and helped interpret and draft the manuscript. All authors read and approved the final manuscript.
This work was financially supported by National Natural Science Foundation of China (Nos. 41371244, and 51278481), Xiamen Science & Technology Major Program (No. 3502Z20131018), and the National High Technology Research and Development Program (“863” Program) of China (No. 2012AA062606).
Compliance with ethical guidelines
Competing interests The authors declare that they have no competing interests.
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