Synthesis, characterization, and photocatalytic activity of MCM-41 and MCM-48 impregnated with CeO2 nanoparticles

Abstract

MCM-41/CeO 2 and MCM-48/CeO 2 were synthesized by direct and indirect methods in solvent media and by grinding method in a solvent-free media. The materials prepared by grinding method are characterized by X-ray diffraction, infrared spectrum analysis, and N 2 adsorption and desorption. Surface areas and pore size of MCM-48/CeO 2 were obtained with values of 680.9 m 2 ·g −1 and 1.64 nm, respectively, by BET method. The results showed that CeO 2 nanoparticles were introduced into MCM-41 and MCM-48, and there was formation of CeO 2 crystallites as secondary phase in the extra framework of MCM-41 and MCM-48. MCM-41/CeO 2 and MCM-48/CeO 2 materials are used as photocatalysts in degradation of Congo red as a dye pollutant. The MCM-41/CeO 2 and MCM-48/CeO 2 prepared by grinding method showed the higher photoreactivity with 97.6 % and 93.1 %, respectively, of degradation of Congo red. The higher photoreactivity is due to the complete incorporation of cerium ions in mesoporous material of MCMs in a solvent-free media.

Background

Ordered mesoporous materials such as MCM-41, MCM-48, and SBAs have been the subject of intensive research in the field of heterogeneous catalysis owing to their high surface area, uniform pores, and relatively high thermal stability [ 1 ]. These materials containing various transition metals are used as heterogeneous catalysts for many organic compound reactions [ 2 , 3 ]. Pure silica mesoporous material has only a few crystal defects and low reaction activity. Because of these disadvantages, researchers attempt to introduce some nanoparticles into this mesoporous material. The successful usages of the transition and rare earth metals in the catalysts are mainly the promoters; in oxides or in the microporous material, some attention have been paid to the combination of the transition and rare earth metals with the mesoporous materials in which the transition and rare earth metals are used as the active components of catalyst [ 2 – 4 ].

Cerium oxide is one of the most reactive rare earth metal oxides, which has been extensively studied and employed in various applications including fast ion conductors, oxygen storage capacitors, catalysts, UV blockers, polishing materials, and electrolytes for solid oxide fuel cells [ 5 ]. CeO 2 or CeO 2 -based materials have also been found to be very important in environmental protection. In particular, supported CeO 2 and CeO 2 -based mixed oxides are effective catalysts for the oxidation of different hydrocarbons and for the removal of organics from polluted water from different sources [ 6 ].

In this study, the impregnation synthesis of MCM-41/CeO 2 and MCM-48/CeO 2 was done using direct and indirect solvothermal and grinding (without solvent) methods. The mesoporous materials of MCM-41 and MCM-48 were synthesized hydrothermally at ambient temperature conditions. A comparative study in structural properties of MCM-41/CeO 2 and MCM-48/CeO 2 materials was evaluated. The performance of these substrates toward the photocatalytic degradation of Congo red in aqueous solution was studied.

Methods

Synthesis of MCM-41 and MCM-48

All of the materials purchased are of highest purity. All solutions were prepared with double distilled water. MCM-41 was synthesized by dispersion of sodium silicate (2.5 g) in deionized water (18.24 ml) [ 7 ]. The surfactant cetyltrimethylammonium bromide (CTAB) was added after stirring the components. The reaction mixture was stirred for 45 min at room temperature. During the vigorous stirring, an adequate amount of 25 % solution of tetramethylammonium hydroxide was added, and the pH was adjusted at 10 to 11. The mixture was stirred at room temperature for 24 h, then introduced into a Teflon-lined autoclave, and kept at a temperature of 100 °C for 3 days. The powder was recovered by filtration, was subsequently washed with acidic water-ethanol solution, and then dried in a vacuum oven. The obtained solid was calcined at 500 °C for 4 h.

Sodium hydroxide and tetraethyl orthosilicate (TEOS) were added to the CTAB solution in the synthesis of MCM-48. The molar composition of the obtained gel is 1 M TEOS:0.25 M Na 2 O:0.65 M CTAB:0.62 M H 2 O [ 8 ]. The solution was stirred for about 1 h, then transferred into a polypropylene bottle, and heated up to 100 °C for 3 days. The product was filtered, washed with water, and dried in air at ambient temperature. The dried product was finally calcined at 550 °C for 6 h.

Synthesis of MCM-41/CeO2 and MCM-48/CeO2 by indirect method

Some polyethylene glycol as dispersant agent was added to the solution of (NH 4 ) 2 Ce(NO 3 ) 6 (0.2134 g), and then 0.1 g of synthesized MCM-41 and/or MCM-48 material was added into the cerium solution. After heating the solution till 40 °C under stirring and adjusting the pH to 7 to 8, ammonium nitrate solution was quickly added, and then the mixed solution was thoroughly stirred for 30 min. After aging for 12 h, the colloid was filtered, washed, and dried in a vacuum oven at 60 °C for 10 h. The synthesized sample was calcined at 600 °C for 5 h in air stream with a heating rate of 10 °C/min [ 9 ]. Cooling it naturally with ambient temperature, MCM-41/CeO 2 (40 wt.%) and MCM-48/CeO 2 (40 wt.%) were gained.

Synthesis of MCM-41/CeO2 and MCM-48/CeO2 by direct method

MCM-41/CeO 2 and MCM-48/CeO 2 were prepared using a modified Stöber's synthesis at room temperature. The weight percent of CeO 2 in prepared materials is 40 %. In a typical synthesis, 12.5 g of hexadecyltrimethylammonium bromide and the required amount (0.2134 g) of ammonium cerium nitrate are taken in a polypropylene bottle. Water and ethanol were added to the obtained mixture, which was stirred well until the dissolution of the metal precursor was completed. To this solution, NH 3 was added followed by 1.8 ml of TEOS. The precipitate obtained was filtered and washed with deionized water extensively. The solid was dried at 80 °C overnight in static air. The dried powder was ground finely and calcined in static air at 550 °C to remove the surfactant molecules for 6 h [ 10 ].

Synthesis of MCM-41/CeO2 and MCM-48/CeO2 by grinding method

In this method, 0.2134 g of (NH 4 ) 2 Ce(NO 3 ) 6 and 0.1 g of synthesized MCM-41 and/or MCM-48 were placed in a mortar and ground drastically at room temperature. The obtained solid was calcined at 550 °C in air for 3 to 4 h to remove the surfactant molecules [ 11 ]. MCM-41/CeO 2 (40 wt.%) and MCM-48/CeO 2 (40 wt.%) were obtained.

Photocatalytic activity of prepared photocatalysts

Photocatalytic degradation of Congo red (CR) was studied at 25 °C and pH = 7 to 8 in the presence of prepared catalysts. The degradation was carried out in a Pyrex photoreactor that has a high pressure mercury lamp of 70 W with maximum irradiation at a wavelength of 332 nm. The degradation was performed at suitable time intervals at room temperature while the samples were stirred continuously. The photoreactor was filled with 25 ml of 10 mg/l CR and 0.7 g/l catalysts. The degradation efficiency (%D) was calculated using initial concentration ( C o ) and residual concentration ( C t ) of CR by spectrophotometric method at λ of 510 nm (%D = [( C o  −  C t )/ C o  × 100). The kinetic rate constant of degradation ( k obs ) was calculated using the model of Langmuir-Hinshelwood's kinetic expression (ln ( C o / C t ) =  k obs t ) [ 12 ].

Results and discussion

Characterization of MCM-41/CeO2 and MCM-48/CeO2

The characterization of MCM-41, MCM-48, MCM-41/CeO 2 , and MCM-48/CeO 2 prepared by grinding method are performed using X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, and Brunauer, Emmett, and Teller (BET) N 2 adsorption-desorption isotherm. The XRD patterns of MCM-41 and MCM-41/CeO 2 samples and MCM-48 and MCM-48/CeO 2 samples are shown, respectively, in Figures 1 and 2 . The hexagonal and cubic ordered structured of MCM-41 and MCM-48, respectively, are confirmed by the XRD patterns [ 9 ].

Figure 1

Small-angle (a) and wide-angle (b) XRD patterns of samples (1) MCM-41 and (2) MCM-41/CeO 2.

Figure 2

Small-angle (a) and wide-angle (b) XRD patterns of samples (1) MCM-48 and (2) MCM-48/CeO 2.

In Figure 1 a, in the small-angle XRD patterns of the prepared material MCM-41, an intense diffraction peak (100), together with an additional peak (110), and a very weak peak (200) were observed. It can be seen that peak (200) is not strong enough and also that the diffraction peaks move to the high angle, and the peaks become weaker when the CeO 2 particles are doped into MCM-41. The increase of CeO 2 particles in the framework of MCM-41 is due to reduction of the tunnel size of the substrate [ 9 – 11 ]. The XRD patterns of MCM-41 and MCM-41/CeO 2 (wide angle) are shown in Figure 1 b. The main substance of MCM-41 is amorphous silica as evident in one diffusion peak observed in the pattern of MCM-41. However, the peak of amorphous silica became weaker, and the peaks of CeO 2 appeared when the CeO 2 nanoparticles are introduced into MCM-41 [ 9 ]. The peaks with 2 θ values of 28.3, 33.2, 47.5 and 56.4 correspond to the (111), (200), (220), and (311) planes [ 13 ].

In the small-angle XRD patterns of MCM-48, the most intense diffraction peak (211) appears at 2 θ  = 2.9° (Figure 2 a), while low intense diffraction peaks are seen at 2 θ  = 3° to 6°. With cerium doping and a gradual loss of long-range ordering of MCM-48, the intensity of the diffraction peak of MCM-48/CeO 2 decreases at a small angle. The diffraction peaks of CeO 2 in the wide-angle XRD pattern have appeared obviously which show the content of CeO 2 in the channel (or in the extra framework) of the sample [ 14 ].

The FT-IR spectra of MCM-41 and MCM-41/CeO 2 are shown in Figure 3 . In the spectra of MCM-41, the stretching vibrating absorption peaks of the O-H band in the surfaced hydroxyl and in the planar water is seen at 3,440 cm −1 . The symmetry and asymmetry flexural vibrating peaks of Si-O-Si at 1,080, 812, and 464 cm −1 , respectively, are related to the framework of silicon [ 9 ]. As seen, there are some differences of the intensities of the peaks in the FT-IR spectra of MCM-41 and MCM-41/CeO 2 , which resulted from the doping of CeO 2 . A strong absorption peak at 1,632 cm −1 is observed in the spectra of MCM-41/CeO 2 , and it indicates the formation of Ce-O-Ce [ 9 ].

Figure 3

FT-IR spectra of (a) MCM-41 and (b) MCM-41/CeO 2 .

Figure 4 shows the FT-IR absorption spectra of the MCM-48 and MCM-48/CeO 2 samples. The absorption bands of asymmetric vibration of Si-O-Si of the silica framework appear at 1,200 and 1,080 cm −1 . The stretching vibration peak of silica is at 815 cm −1 . The vibration band at 1,080 cm −1 are shifted 4 to 9 cm −1 for the MCM-48/CeO 2 sample compared with the spectrum of MCM-48. This shift is due to the incorporation of Ce into the framework of MCM-48 [ 14 ].

Figure 4

FT-IR spectra of (a) MCM-48 and (b) MCM-48/CeO 2 .

The N 2 adsorption and desorption isotherms of the MCM-48/CeO 2 sample is shown in Figure 5 , and the corresponding pore size distribution curve is shown in Figure 6 . It is shown that these isotherms have the typical characteristics of the mesoporous material isotherm and are of the type IV according to the IUPAC classification [ 14 ]. The BET surface areas, average pore size calculated by the BJH model, and the pore volume of MCM-48 [ 14 ] and MCM-48/CeO 2 samples are presented in Table 1 .

Figure 5

Nitrogen adsorption and desorption isotherms of MCM-48/CeO 2.

Figure 6

Pore size distribution curves of MCM-48/CeO 2.

Table 1

Textural properties of MCM-48 and MCM-48/CeO 2 samples

Sample

Surface area (m2·g−1)

Pore volume (cm3·g−1)

Pore size (nm)

MCM-48

895.0

0.850

2.23

MCM-48/CeO2

680.9

0.398

1.64

Photocatalytic degradation of Congo red

The control experiment indicates that CR was not degraded completely when irradiated with UV in the absence of a catalyst; only 24.7 % was degraded after 120 min. The primary factor of photocatalytic degradation is the adsorption of CR onto the catalyst surface via the interaction of surface hydroxyl groups, particularly onto high-surface area support, i.e., MCM-41 and MCM-48 [ 15 ]. In other words, the adsorption of anionic dye on oxide surface is favored, leading to an increase of the dye concentration on the surface and the facilitation of photocatalytic degradation of the dye being investigated [ 16 , 17 ]. The presence of transition metal cations such as cerium doped on the mesoporous materials, such as MCM-41 and MCM-48, may prevent the recombination between the photogenerated holes and electrons or elongate the time of charge separation because it acts as an electron acceptor center [ 18 , 19 ]. One can assumed that the hydroxyl groups on the surface of prepared catalysts act as an electron donor for photogenerated H + , forming active hydroxyl radicals (OH˙ + ) which attack the CR.

Table 2 shows the performances of MCM-41/CeO 2 and MCM-48/CeO 2 (prepared by different methods) and nanoparticles of CeO 2 as photocatalysts for the photocatalytic degradation of CR in 120 min. The k obs values are also collected in Table 2 . Among the prepared catalysts, the mesoporous MCM-41/CeO 2 and MCM-48/CeO 2 that were synthesized by grinding method show the most photocatalytic activity with 97.6 % and 91.3 % photodegradation of CR, respectively. Apparently, the most cerium ions are doped in mesoporous materials by grinding method, and the weight percentage of CeO 2 in MCM/CeO 2 is near 40 % which is in accordance to what was mentioned in the ‘Methods’ section. However, a lot of cerium ions have been lost in the preparation of MCM/CeO 2 by direct and indirect methods in a solvent medium.

Table 2

CR degradation in 120 min and k obs of photocatalytic process over CeO 2 , MCM-41/CeO 2 , and MCM-48/CeO 2

Catalysts

%D

kobs × 10−3(min−1)

Without photocatalyst

24.7

1.9

CeO2

51.9

6.0

MCM-41/CeO2, direct method

44.2

5.0

MCM-48/CeO2, direct method

37.6

3.7

MCM-41/CeO2, indirect method

52.7

6.0

MCM-48/CeO2, indirect method

46.7

5.4

MCM-41/CeO2, grinding method

97.6

36.0

MCM-48/CeO2, grinding method

91.3

22.7

The amount of CR degraded on the surface of the different catalysts showed the order of sequence: MCM-41/CeO 2  > MCM-48/CeO 2  > CeO 2 , which can be directly related to the surface area that is available for adsorption. As for CeO 2 nanoparticles, they show 51.9 % of degradation. However, good photodegradation is obtained over the MCMs/CeO 2 catalyst. The enhanced photocatalytic activity over the composite MCMs/CeO 2 is reflecting the beneficial adsorption properties of MCM-41 and MCM-48. Thus, it is clear that the presence of cerium in MCM-41/CeO 2 and MCM-48/CeO 2 plays a role in the catalytic reaction, that is to say, the Ce ions that dispersed highly in MCM/CeO 2 are the active sites. The enhancements of CR degradation may be due to the high dispersion of CeO 2 in the amorphous wall of MCM-41 and MCM-48 and the increase of the bandgap between the conduction band and valance band of CeO 2 in MCMs. In addition, due to the wide bandgap of MCM-41/CeO 2 and MCM-48/CeO 2 , the lifetime of photogenerated holes and electrons of the MCMs/CeO 2 is longer than that of CeO 2 nanoparticles [ 20 – 22 ].

The higher activity of MCM-41/CeO 2 may be due to the hexagonal ordered structured compared to MCM-48 with cubic ordered structured [ 21 , 22 ]. The hexagonal ordered structured of MCM-41 due to the higher dispersion of cerium on this sample.

Conclusions

The grinding method can be used to prepare cerium-doped MCM-41 and MCM-48 mesoporous materials. Using this method, certain cerium cations can be incorporated into the framework of MCM-41 and MCM-48. After CeO 2 particles are being doped into substrates of MCM-41 and MCM-48, the surface area of the material was reduced, and the pore volume also decreased. The prepared MCM-41/CeO 2 and MCM-48/CeO 2 show the photoreactivity in CR degradation. The hexagonal structure of MCM-41 has a larger surface area and has active sites. Also, there are CeO 2 nanoparticles in the secondary phase in the extra framework of mesoporous materials. Thus, the MCM-41/CeO 2 catalyst exhibits the higher reactivity in comparison with MCM-48/CeO 2 .

Authors' information

HRP is an associate professor of Chemistry, and MA is an M.Sc. student of Chemistry.

Acknowledgments

The authors are grateful to the Malek-Ashtar University of Technology and Islamic Azad University, Shahreza Branch for the financial support of this work.

Competing interests

The authors declare that they have no competing interest.

Authors' contribution

Both authors participated in the experiments, read and approved the final manuscript.

References

  1. Kresge et al. (1992) Ordered mesoporous molecular sieves synthesized by a liquid-crystal template mechanism (pp. 710-712) 10.1038/359710a0
  2. Kawabata et al. (2005) Iron-containing MCM-41 catalysts for Baeyer–Villiger oxidation of ketones using molecular oxygen and benzaldehyde (pp. 99-106) 10.1016/j.molcata.2005.03.027
  3. Koo et al. (2005) WO3 nanoparticles on MCM-48 as a highly selective and versatile heterogeneous catalyst for the oxidation of olefins, sulfides, and cyclic ketones (pp. 5015-5018) 10.1021/ol052019i
  4. Moller and Bein (1998) Inclusion chemistry in periodic mesoporous hosts (pp. 2950-2963) 10.1021/cm980243e
  5. Wang and Feng (2003) Polyhedral shapes of CeO2 nanoparticles (pp. 13563-13566) 10.1021/jp036815m
  6. Monteiro et al. (2001) The role of Pd precursors in the oxidation of carbon monoxide over Pd/Al2O3 and Pd/CeO2/Al2O3 catalysts (pp. 77-89) 10.1016/S0920-5861(00)00547-2
  7. Nazari et al. (2005) Iron(III)protoporphyrin/MCM41 catalyst as a peroxidase enzyme model: preparation and typical test reactions (pp. 1-9) 10.1016/j.molcata.2005.05.010
  8. Kumar et al. (2001) MCM-41, MCM-48 and related mesoporous adsorbents: their synthesis and characterization (pp. 109-116) 10.1016/S0927-7757(01)00638-0
  9. Song et al. (2008) Synthesis and characterization of MCM-41 materials assembled with CeO2 nanoparticles (pp. 193-196) 10.1016/j.colsurfa.2007.05.040
  10. Subramanian et al. (2010) Baeyer–Villiger oxidation of cyclic ketones using Fe containing MCM-48 cubic mesoporous materials (pp. 66-72) 10.1016/j.molcata.2010.07.003
  11. Li and Yan (2010) Functionalized mesoporous SBA-15 with CeF3: Eu3+ nanoparticle by three different methods: synthesis, characterization, and photoluminescence (pp. 701-708) 10.1007/s11671-010-9534-0
  12. Al-Ekabi and Serpone (1988) Kinetic studies in heterogeneous photocatalysis (pp. 5726-5731) 10.1021/j100331a036
  13. Pouretedal and Kadkhodaie (2010) Synthetic CeO2 nanoparticle catalysis of methylene blue photodegradation: kinetics and mechanism (pp. 1328-1334) 10.1016/S1872-2067(10)60121-0
  14. Wangcheng et al. (2008) Synthesis of cerium-doped MCM-48 molecular sieves and its catalytic performance for selective oxidation of cyclohexane (pp. 515-522) 10.1016/S1002-0721(08)60129-5
  15. Wang and Li (2004) Structure directed reversible adsorption of organic dye on mesoporous silica in aqueous solution (pp. 21-26) 10.1016/j.micromeso.2006.08.005
  16. Fu et al. (2004) Preparation of activated carbon fibers supported TiO2 photocatalyst and evaluation of its photocatalytic reactivity (pp. 81-88) 10.1016/j.molcata.2004.06.018
  17. El-Sheikh et al. (2004) Deposition of anatase on the surface of activated carbon (pp. 284-292) 10.1016/j.surfcoat.2004.03.012
  18. Mohamed and Al-Esaimi (2006) Characterization, adsorption and photocatalytic activity of vanadium-doped TiO2 and sulfated TiO2 (rutile) catalysts: degradation of methylene blue dye (pp. 5361-5367) 10.1016/j.molcata.2006.03.071
  19. Chu et al. (2004) Design and elaboration of new solid acids for the synthesis of butylacetate (pp. 349-353) 10.1016/j.cattod.2004.04.046
  20. Ji et al. (2008) Ordered mesoporous CeO2 synthesized by nanocasting from cubic Ia3d mesoporous MCM-48 silica: formation, characterization and photocatalytic activity (pp. 17809-17813) 10.1021/jp8054087
  21. Hadjiivanov et al. (2003) Characterization of Cu/MCM-41 and Cu/MCM-48 mesoporous catalysts by FTIR spectroscopy of adsorbed CO (pp. 331-340) 10.1016/S0926-860X(02)00510-0
  22. Sakthivel et al. (2001) Mesoporous (Cr)MCM-41 and (Cr)MCM-48 molecular sieves: promising heterogeneous catalysts for liquid phase oxidation reactions (pp. 155-158) 10.1023/A:1012711801043