Next Article in Journal
Effect of Storage in Distilled Water for Three Months on the Antimicrobial Properties of Poly(methyl methacrylate) Denture Base Material Doped with Inorganic Filler
Previous Article in Journal
Stability and Hydrocarbon/Fluorocarbon Sorption of a Metal-Organic Framework with Fluorinated Channels
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Materials
Volume 9
Issue 5
10.3390/ma9050326
materials-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Facile Synthesis of CeO2-LaFeO3 Perovskite Composite and Its Application for 4-(Methylnitrosamino)-1-(3-Pyridyl)-1-Butanone (NNK) Degradation

by
Kaixuan Wang
1,
Helin Niu
1,*,
Jingshuai Chen
1,
Jiming Song
1,
Changjie Mao
1,
Shengyi Zhang
1,
Saijing Zheng
2,
Baizhan Liu
2 and
Changle Chen
3,*
1
Anhui Province Key Laboratory of Environment-Friendly Polymer Materials, School of Chemistry and Chemical Engineering, Anhui University, Hefei 230601, China
2
Key Laboratory of Cigarette Smoke Research of China National Tobacco Corporation, Shanghai 200082, China
3
CAS Key Laboratory of Soft Matter Chemistry, Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei 230026, China
*
Authors to whom correspondence should be addressed.
Materials 2016, 9(5), 326; https://doi.org/10.3390/ma9050326
Submission received: 23 February 2016 / Revised: 26 April 2016 / Accepted: 26 April 2016 / Published: 29 April 2016
Browse Figures
Versions Notes

Abstract

:
A facile and environmentally friendly surface-ion adsorption method using CeCO3OH@C as template was demonstrated to synthesize CeO2-LaFeO3 perovskite composite material. The obtained composite was characterized by X-ray diffraction (XRD), fourier transform infrared spectra (FT-IR), field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), thermo-gravimetric analysis and differential scanning calorimetry (TG-DSC), N2 adsorption/desorption isotherms and X-ray photoelectron spectra (XPS) measurements. The catalytic degradation of nitrosamine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) was tested to evaluate catalytic activity of the CeO2-LaFeO3 composite. Much better activity was observed for the CeO2-LaFeO3 composite comparing with CeO2 and LaFeO3. These results suggested that perovskite composite materials are a promising candidate for the degradation of tobacco-specific nitrosamines (TSNAs).

1. Introduction

Perovskite materials can be described as ABO3, with A and B being two cations and O being an oxygen anion. Perovskite materials are well known for their advantageous physical and chemical properties for various applications such as catalysts [1,2], multiferroic materials [3], energy conversion materials [4,5], and gas sensors [6]. Recently, LaFeO3 and related materials have received increasing attention [7,8]. CeO2 has been extensively studied as a catalyst to transform some environmentally harmful substances into environmentally friendly materials, such as oxidation CO [9], selective reduction of NO [10] and photocatalytic degradation of Rhodamine B [11]. Therefore, it is highly fascinating to combine the advantages of LaFeO3 and CeO2 materials [12,13]. A variety of techniques have been developed to fabricate the CeO2-LaFeO3 composite materials, such as the solid-state reaction method [14], solution combustion and co-precipitation method [15], low-temperature thermal decomposition method [16] and ethylene diamine tetraacetic acid-citrate method [17]. In this work, we reported a facile and environmentally friendly surface-ion adsorption method to prepare perovskite-type LaFeO3 and a CeO2-LaFeO3 composite. The formation mechanism was also investigated.
Tobacco smoke contains more than 5000 kinds of compounds. Among these chemicals, tobacco-specific nitrosamines (TSNAs) play a significant role in causing lung cancer and other diseases for people who either use tobacco products or are exposed to secondhand smoke [18]. There are mainly four kinds of tobacco-specific nitrosamines: 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), N’-nitrosonornicotine (NNN), N’-nitrosoanatabine (NAT) and N’-nitrosoanabasine (NAB) [19], of which NNK has been identified as the most potent lung carcinogen [20,21]. In order to protect public health, it is necessary to reduce the level of NNK in tobacco. Control of the storage environment, reduction of leaf nitrate contents, and the scavenging of gaseous nitrosating agents could be especially effective to reduce or inhibit NNK formation during the storage of cured tobacco [22]. Zeolites were successfully applied to capture and degrade NNK in gas or liquid phases [19,23]. Nanostructured titanates were also used as catalysts for selectively reducing NNK in mainstream cigarette smoke [24]. These results suggest that it is possible to efficiently degrade NNK contents with suitable catalysts. Since all TSNA materials contain N-NO group, it was hypothesized that the catalytic breaking of the chemical bond in the N-NO group by perovskite materials may be the key step for the decomposition of these carcinogens [19]. In this work, we preformed systematic studies on the properties of CeO2-LaFeO3 composite for the degradation of NNK.

2. Results and Discussion

Figure 1A shows the X-ray powder diffraction (XRD) patterns of (a) CeO2; (b) LaFeO3; (c) CeO2-LaFeO3 precursor; and (d) CeO2-LaFeO3. The samples were scanned from 2θ degrees of 20° to 90°, using a Cu Kα radiation with a characteristic wavelength (λ) of 0.15405 nm. As shown in Figure 1A-a, the main characteristic peaks located at 2θ = 28.55°, 47.48°, 56.34° are corresponding to the (111), (220), (311) planes of CeO2, which are in good agreement with the reported XRD data (JCPDS Card No. 43-1002). All of these peaks are corresponding to a face-centered cubic (fcc) fluorite structure CeO2 [25]. Figure 1A-b can be assigned to the orthorhombic perovskite LaFeO3 structure with the Pbnm space group, and the diffraction peaks completely agree with those of JCPDS Card No. 37-1493. No obvious peak could be observed in the XRD pattern of CeO2-LaFeO3 precursor (Figure 1A-c), indicating that neither LaFeO3 nor CeO2 were formed after ultrasonic-assisted surface-ion adsorption treatment. In Figure 1A-d, the main diffraction peaks at 2θ = 22.61°, 32.19°, 39.67°, 46.14° and 57.39° belong to the LaFeO3 orthorhombic perovskite phase and the weak signals at 2θ = 28.55°, 47.48°, 56.34° correspond to the CeO2 phase concurrent with the major perovskite phase. These results indicate the formation of a CeO2-LaFeO3 composite. The main diffraction peak of the obtained CeO2-LaFeO3 was almost the same as that of LaFeO3. However, the peak slightly shifted to a lower angle (inset of Figure 1A), indicating an enlarged dimension of unit cell caused by the cerium substitution [26]. The crystallite size of the catalysts was estimated using Scherrer’s method as follows [27]:
D = Kλ/βcosθ
where D is the average diameter of the calculated particles; K is the shape factor of the average grain size (the expected shape factor is 0.89), λ is the wavelength characteristic in Å (in this particular case λ = 1.5405 Å); and β is the width of the X-ray peak at half height. The average crystallite size of CeO2, LaFeO3 and CeO2-LaFeO3 samples was found to be 12, 24 and 17 nm, respectively. In the CeO2-LaFeO3 composite, the diffraction peak for the CeO2 phase is extremely weak. Therefore, the average crystallite size in the CeO2-LaFeO3 composite was determined using the main reflections (2θ = 22.61°, 32.19°) corresponding to the LaFeO3 phase.
The FT-IR spectra of CeCO3OH@C, CeO2-LaFeO3 precursor and CeO2-LaFeO3 are shown in Figure 1B. The absorption peak centered at ca. 3410 cm−1 was attributed to the structural O-H stretching vibration modes of physically absorbed H2O on the samples or the surface O-H group in the materials, whereas the absorption peaks at ca. 2922 cm−1 and ca. 2852 cm−1 were attributed to C-H asymmetric and symmetric stretching vibrations. The absorption peaks at 1796 cm−1 were attributed to (COO−). The absorption peaks at ca. 1628 cm−1 (Figure 1B-a,b) were attributed to C=C vibrations [28,29], which became weaker after calcination (Figure 1B-c). The absorption peaks at ca. 1384 cm−1 were attributed to -CH3 symmetrical deformation vibration (Figure 1B-a,c). The peak being stronger (Figure 1B-b) was due to stretching vibration of nitrate anion adsorbed on the CeO2-LaFeO3 precursor surface, which overlapped with -CH3 symmetrical deformation vibration. The peak becoming weaker (Figure 1B-c versus Figure 1B-b) was ascribed to the decomposing of nitrate anions. The bands in the 504−730 cm−1 region (Figure 1B-c) were assigned to the stretching modes of the octahedral FeO6 groups in perovskite, which were the most important absorption bands of the perovskite structure [30]. The band located at ca. 453 cm−1 (Figure 1B-c) can be assigned to the deformation modes of the same polyhedra [31]. However, no peaks of CeO2 were detected. Based on the FT-IR analysis, it can be concluded that CeCO3OH@C possesses hydrophilic negatively charged groups such as -OH and -COO− on its carbonaceous shell, and these groups can cause adsorption metal cations in aqueous solution. Through the subsequent calcination process, the carbonaceous shell could be eliminated and the composite formed. Therefore, CeCO3OH@C can be used as a template to synthesize perovskite composites.
The TG-DSC curves of LaFeO3 precursor and CeO2-LaFeO3 precursor were shown in Figure 1C,D. The total weight loss of LaFeO3 precursor (Figure 1C) was 89.70%, indicating a 10.30% LaFeO3 product yield. The sharp exothermic peak at 298 °C in the DSC curve corresponds to the heat generated by the burning of the carbonaceous spheres’ template and decomposing of nitrate anions [32]. The broad exothermic peak at about 348 °C can be attributed to the crystallization process of LaFeO3 [33]. The total weight loss of the as-prepared CeO2-LaFeO3 precursor was 76.92%. The broad exothermic peak at about 320 °C and the sharp exothermic peak at about 487 °C correspond to the combustion of carbon-rich polysaccharide (GCP) and formation of CeO2-LaFeO3.
The representative SEM and TEM images of the carbonaceous spheres and CeCO3OH@C templates are shown in Figure 2. After hydrothermal treatment, carbonaceous spheres formed and displayed good monodispersed spherical morphology with an average diameter of 150 nm (Figure 2A,B). Figure 2C,D are the SEM and TEM images of CeCO3OH@C. The GCP-coated CeCO3OH nanospheres were well retained. Figure 3D shows that CeCO3OH@C has a CeCO3OH core; a GCP shell has been prepared by the hydrothermal method. To some degree, the structure of GCP-coated CeCO3OH nanospheres have overlapped with the shell, which is a similar result to our previous work [27].
The representative SEM and TEM images of LaFeO3, CeO2 and CeO2-LaFeO3 are shown in Figure 3. The SEM image of LaFeO3 (Figure 3A) obtained by calcining the LaFeO3 precursor possesses a small branch-shape structure which consists of many small nanorods. The TEM result also indicates that the LaFeO3 (Figure 3B) nanostructure was stacking by smaller LaFeO3 nanorods with an average diameter of 24 nm (calculated by using Scherrer equation). In the SEM image (Figure 3D), CeO2 nanoparticles exhibit uniform size distribution and spherical morphology. The TEM image (Figure 3D) indicated that the sample is composed of tiny nanocrystallites (about 12 nm, calculated by using the Scherrer equation). The SEM image of CeO2-LaFeO3 (Figure 3E) displays an irregular porous structure. The morphology of CeO2-LaFeO3 also displays an irregular porous structure in the TEM image (Figure 3F).
Brunauer-Emmett-Teller (BET) analysis was used to investigate the specific surface area of the samples. The specific surface areas of CeO2, LaFeO3 and CeO2-LaFeO3 are 47.3, 24.7 and 12.7 m2·g−1, respectively. The N2 isotherm of CeO2-LaFeO3 shown in Figure 4 is close to Type IV (according to International Union of Pure and Applied Chemistry classification) with a hysteresis loop observed in the range of 0.4–1.0 p/p0, indicating the mesoporous structure of the CeO2-LaFeO3 composite.
The oxidation states of principal elements of LaFeO3 were analyzed by XPS. All the binding energy values obtained in the XPS analysis were calibrated using C 1s (284.8 eV) as the reference. Figure 5A–E display the XPS spectra of La 3d5/2, Fe 2p, Ce 3d and O 1s and C 1s core levels for the as-prepared CeO2, LaFeO3 and CeO2-LaFeO3. The peaks of La 3d5/2 and La 3d3/2 for LaFeO3 in Figure 5A are situated at 833.9 and 837.5 eV and at 851.1 and 854.6 eV, while the peaks of La 3d5/2 and La 3d3/2 for CeO2-LaFeO3 in Figure 5A are situated at 833.6 and 837.4 eV and at 850.42 and 854.5 eV. These results confirm the presence of La3+ ions [34]. In Figure 5B, the peaks at 710.8 and 724.1 eV of LaFeO3 are attributed to the binding energies of Fe 2p3/2 and 2p1/2, while the peaks at 710.6 and 724.2 eV of CeO2-LaFeO3 are attributed to the binding energies of Fe 2p3/2 and 2p1/2, respectively. No noticeable shoulder peaks are found in the Fe 2p XPS spectrum, indicating that Fe ions are in the Fe3+ oxidation state [35]. The Ce 3d transition peaks of CeO2 and CeO2-LaFeO3 composites are shown in Figure 5C. The v0, v’, u0, and u’ peaks are attributed to Ce3+, whereas v, v’’, v’’’, u, u’’, and u’’’ are attributed to Ce4+. The Ce4+/Ce3+ atomic ratio has been obtained from the area of the peaks obtained by the deconvolution procedure [36]. In this way, a Ce3+/(Ce4+ + Ce3+) ratio of 0.32 has been obtained on the CeO2 sample, while the amount of Ce3+ species increases on the CeO2-LaFeO3 composite (Ce3+/(Ce4+ + Ce3+) atomic ratio of 0.39). Especially the state of O 1s indicated that there are two sorts of oxygen on the surface, the lattice oxygen (OL) and the adsorbed oxygen (Oads). For O ions in LaFeO3, the broad and asymmetric O 1s XPS spectra correspond to two kinds of oxygen chemical states according to the binding energy range. The peak at approximately 529.0 eV is attributed to OL and the other broad peak at around 531.6 eV is attributed to Oads, indicating that it is attributed to the contribution of La-O and Fe-O in LaFeO3 crystal lattice for the OL signal [34]. For O ions in CeO2, Figure 5D shows that the O 1s spectra for the sample contain one band located at 529.1 eV and a shoulder at the higher binding energy of 531.5 eV. The former is originated from lattice oxygen (Ce-O) and the latter can be attributed to the adsorbed oxygen [25]. As for CeO2-LaFeO3, the O 1s spectra (Figure 5D) also shows a major peak at the 529.3 eV and a broad shoulder peak around 531.5 eV, attributed to the lattice oxygen O2− (La-O, Fe-O and Ce-O) and adsorbed oxygen species. The C1s peaks are presented in Figure 5E.
The atomic concentration ratios were also obtained by XPS. The different atomic concentration ratios on the surface of as-prepared catalysts were calculated and are listed in Table 1. In addition, the Fe/La ratio of LaFeO3 (1.2, see Table 1) and CeO2-LaFeO3 (1.35, see Table 1) are slightly higher than theoretical value indicating that excess amount of iron appears on the surface of LaFeO3, which is different from the results of Wei et al. [37]. The reason is not clear and needs to be examined further. We suspect that such a result is likely related to the different preparation methods employed compared to those of Wei et al.
The adsorption and catalytic degradation of nitrosamine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) were investigated to evaluate catalytic activity of CeO2-LaFeO3. Liquid adsorption results are listed in Figure 6A. Compared with the Blank experiment without any catalyst, the adsorption performance of the three catalysts followed the order of CeO2-LaFeO3 (33.85%) > CeO2 (28.85%) > LaFeO3 (23.35%). The degradation of NNK using different catalysts is displayed in Figure 6A. Compared to the blank experiment without any catalyst, the catalytic performance of the three catalysts followed a sequence of CeO2-LaFeO3 > LaFeO3 > CeO2. The degradation ratio of NNK is 76.78% for CeO2-LaFeO3, 58.09% for CeO2 and 64.12% for LaFeO3. In summary, CeO2-LaFeO3 composite trapped more NNK (33.85 μg·g−1) than CeO2 (22.85 μg·g−1) and LaFeO3 (23.35 μg·g−1), despite the former having the smallest specific surface area among the three catalysts. The catalytic activity per surface area of CeO2-LaFeO3, CeO2 and LaFeO3 to NNK were tested to be 6.05, 1.23, 2.60 μg·m−2, respectively. MCM-22 could adsorb 54% nitrosamines in solution [38], and SBA-15 could catalytically degrade 65% nitrosamines [39]. However, the specific surface of zeolites usually displays 1−2 orders of magnitude higher than perovskite materials. The actual adsorption ability of per m2 surface area of CeO2-LaFeO3 composite is superior to zeolites. What is more, the preparation processes for zeolites consume a large amount of strong acid or base, which is harmful to the environment. Additionally, the high cost of zeolites is a disadvantage for industry application. Conversely, the CeO2-LaFeO3 composite possesses the advantages of being environmentally friendly, easy to synthesize, inexpensive to prepare, thermally stable and potentially easy to industrialize.
The resonance structure of NNK is shown in Figure 6B and the possible adsorption and degradation mechanism is shown in Figure 6C. NNK possesses the N-N=O functional group, which could be adsorbed on CeO2-LaFeO3 surface through electrostatic interaction. The catalytic degradation of NNK probably starts from the rupture of the N-N bond in the N-N=O group [39]. Under the same conditions, the CeO2-LaFeO3 composite showed superior properties to the other two catalysts. This may originate from the synergistic effect of CeO2-LaFeO3 for degradation of NNK. In the nominal composite CeO2-LaFeO3 perovskite structure, some Ce3+ ions may substitute the La3+ ion in the A-site of the LaFeO3 perovskite structure. From the XPS result (the Ce3+/(Ce4+ + Ce3+) atomic ratio on the CeO2-LaFeO3 composite is higher than pure CeO2), it was confirmed that the Ce3+ ion exists in La1−xCexFeO3 crystal phases. Because of the introduction of the Ce3+ ion, stronger interactions occur between Fe ions and the adsorbed O2. Correspondingly, O2 is activated and may lead to higher oxidative reactivity than pure LaFeO3 [12], resulting in higher activity for the CeO2-LaFeO3 composite. Furthermore, CeO2 has high oxygen storage capacity, high oxygen mobility and facile reducibility [16]. The synergistic effect of the LaFeO3 perovskite structure and CeO2 redox property play a crucial role in enhancing the degradation efficiency of NNK. Consequently, the performance for degradation of NNK followed the order of CeO2-LaFeO3 > LaFeO3 > CeO2.

3. Experimental Section

3.1. Materials

4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) were purchased from Toronto Research Chemical Inc. (Toronto, ON, Canada). La(NO3)3·6H2O, Ce(NO3)3·6H2O, glucose, urea, Fe(NO3)3·9H2O were purchased from Shanghai Chemical Reagent Company (Shanghai, China). All the chemicals were analytical pure grade and were used as received without further purification. Deionized water was used throughout the experiments.

3.2. Synthesis

Based on our previous experiments [40], a typical synthesis method was taken after minor changes: 0.5 M glucose was sealed in a Teflon-lined stainless steel autoclave with 100 mL capacity and maintained at 180 °C for 6 h. After cooling down naturally, the precipitate was harvested by centrifugation and washed thoroughly with deionized water and ethanol. After drying at 60 °C overnight, carbonaceous spheres were obtained. The amounts of 2.18 g La(NO3)3·6H2O and 2.02 g Fe(NO3)3·9H2O were dissolved in 20 mL water. After magnetic stirring for 10 min, 1.00 g carbonaceous spheres were added into the above solution. The solution was subsequently treated ultrasonically at 600 W for 45 min. The resulting solution was aged at room temperature overnight to achieve adsorption-desorption equilibrium between carbonaceous spheres with Fe3+ and La3+ ions and then centrifuged. After drying at 60 °C overnight, the obtained precursor was denoted as the LaFeO3 precursor. The LaFeO3 precursor was calcined at 700 °C for 2 h and the LaFeO3 was obtained.
Uniform-sized CeCO3OH@C nanospheres were synthesized by a hydrothermal method. In a typical synthesis, 0.63 g Ce(NO3)3·6H2O, 5.07 g glucose and 0.86 g urea were dissolved in 100 mL water with magnetic stirring. The solution was transferred into a 100 mL Teflon-lined stainless steel autoclave and hydrothermally treated at 180 °C for 2 h. After cooling down naturally, the precipitate was harvested by centrifugation and washed thoroughly with deionized water and ethanol. After drying at 60 °C overnight, CeCO3OH@C was obtained. A certain amount of CeCO3OH@C was calcined in a muffle furnace at 550 °C for 2 h to obtain CeO2 nanospheres.
In a typical process, 2.18 g La(NO3)3·6H2O and 2.02 g Fe(NO3)3·9H2O were dissolved in 20 mL water with magnetic stirring. Subsequently, 1.00 g CeCO3OH@C was added into the above solution and evenly dispersed with the assistance of magnetic stirring. The solution was treated ultrasonically at 600 W for 45 min. The resulting solution was aged at room temperature overnight to achieve adsorption-desorption equilibrium between CeCO3OH@C, Fe3+ and La3+ ions. The solution was centrifuged and washed thoroughly with deionized water and ethanol. The obtained precursor was dried in an oven at 60 °C overnight and denoted as the CeO2-LaFeO3 precursor. The precursor was calcined at 700 °C for 2 h to obtain CeO2-LaFeO3 composite. The formation process of CeO2-LaFeO3 composite is illustrated in Scheme 1. First, La3+ and Fe3+ are incorporated into CeCO3OH@C hydrophilic shell since the surface of CeCO3OH@C possesses hydrophilic groups. Second, after calcination, the hydrophilic shell was eliminated and CeO2-LaFeO3 composite formed. After calcination at 700 °C for 2 h, the spherical structure collapsed and a porous nanostructure formed.

3.3. Degradation of 4-(Methylnitrosamino)-1-(3-Pyridyl)-1-Butanone (NNK) by CeO2-LaFeO3

The catalytic activity for the degradation of NNK by CeO2-LaFeO3 was performed as follows: 50 mg catalyst was dispersed ultrasonically in 5 mL of 1 μg·mL−1 NNK/methanol solution. After that, all of the solutions were evenly dispersed on the same mass quantitative filter papers several times and dried at 30 °C. Quantitative filter papers were made into cigarette shapes and smoked by using a smoking machine. The smoke and the particles after ignition were thoroughly absorbed, extracted, purified, and then transferred to a 25 mL volumetric flask and diluted with methanol to volume. Finally, the diluted methanol solution was analyzed by Agilent 6460 Triple Quad Liquid chromatography-Mass Spectrum (LC/MS, Agilent Technologies, Santa Clara, CA, USA). LaFeO3 and CeO2 were also tested. As a control experiment, 5 mL of 1 μg·mL−1 NNK/methanol solution without catalyst was also tested.
Liquid adsorption of NNK was performed as follows: 20 mg LaFeO3, CeO2 and CeO2-LaFeO3 were added into 10 mL of 0.2 μg·mL−1 NNK/methanol solution, respectively. The solutions were treated ultrasonically for 1 h and centrifuged at 5000 rpm for 10 min. As a control, 10 mL of 0.2 μg·mL−1 NNK/methanol solution without catalyst was also tested. The residual quantity of NNK in absorbed methanol was carried out using Agilent 6460 Triple Quad LC/MS. The mass ratio of catalyst to NNK remained the same (catalyst: NNK = 10 mg:1 μg) in the catalytic and adsorption experiments.

3.4. Characterization

X-ray powder diffraction of the as-prepared materials were characterized by X-ray diffraction (XRD, Rigaku D/max-RA, Tokyo, Japan, graphite monochromatized Cu Kα radiation, λ = 1.5406 Å, at 36 kV). FT-IR spectra were recorded with a Nicolet MAGNA-IR 750 instrument (KBr disks, Nicolet Instrument, Madison, WI, USA) in the 4000–400 cm−1 regions. Morphologies of samples were examined by field-emission scanning electron microscopy (FE-SEM, Hitachi S4800, Hitachi, Hitachi, Japan). Transmission electron microscopy (TEM) was obtained by a JEM-2100 transmission electron microscope (JEOL, Tokyo, Japan). Thermo-gravimetric analysis and differential scanning calorimetry (TG-DSC) data was recorded with a thermal analysis instrument (WCT-1D, BOIF, Beijing, China) under an airflow atmosphere at the heating rate of 10 °C·min−1 from room temperature to 800 °C. Specific surface areas and sorption isotherms of the samples were measured via a nitrogen sorption system at 77 K on a Micromeritics ASAP 2020 analyzer (Norcross, Atlanta, GA, USA). The specific surface area was calculated by the Brunauer-Emmett-Teller (BET) method. The X-ray photoelectron spectra (XPS) were taken on an ESCALab MKII X-ray photoelectron spectrometer (Thermo VG Scientific, West Sussex, UK) to obtain further evidence for the purity and composition of the as-prepared products, using Al Ka radiation as the exciting source.

4. Conclusions

In summary, LaFeO3 and CeO2-LaFeO3 porous structured perovskite mixed oxides were successfully synthesized by a novel surface-ion adsorption method using carbonaceous microspheres and CeCO3OH@C as templates. The surface-ion adsorption method could be a promising method to synthesize various perovskite composite materials. The performance for degradation of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) followed a sequence of CeO2-LaFeO3 > LaFeO3 > CeO2. The CeO2-LaFeO3 composite exhibited excellent catalytic activity for NNK degradation, making it a promising candidate for environmentally friendly applications. Based on these results, other catalysts with structures similar to CeO2-LaFeO3 may also be used for the degradation of tobacco-specific nitrosamines (TSNAs) such as NNK in tobacco. Furthermore, the investigations of other Ce-doped perovskite materials, such as CeO2-LaCoO3 and CeO2-LaNiO3 for the degradation of NNK, are in progress.

Acknowledgments

This work was supported by the Key Laboratory of Cigarette Smoke Research of China National Tobacco Corporation (CF-ZJ2) and the National Natural Science Foundation of China (Grant Nos. 21471001, 21275006 and 21575001), Key Project of Anhui Provincial Education Department (KJ2013A029) and Natural Science Foundation of Anhui Province (1508085MB32).

Author Contributions

Kaixuan Wang, Jingshuai Chen, Jiming Song, Changjie Mao, Shengyi Zhang, Saijing Zheng, Baizhan Liu performed the preparation of the samples, the characterizations and the catalytic studies. Helin Niu and Changle Chen conceived and supervised the project. Helin Niu and Changle Chen wrote the manuscript with contributions from all authors.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Royer, S.; Duprez, D.; Can, F.; Courtois, X.; Batiot-Dupeyrat, C.; Laassiri, S.; Alamdari, H. Perovskites as Substitutes of Noble Metals for Heterogeneous Catalysis: Dream or Reality. Chem. Rev. 2014, 114, 10292–10368. [Google Scholar] [CrossRef] [PubMed]
  2. Zhu, J.J.; Li, H.L.; Zhong, L.Y.; Xiao, P.; Xu, X.L.; Yang, X.G.; Zhao, Z.; Li, J.L. Perovskite Oxides: Preparation, Characterizations, and Applications in Heterogeneous Catalysis. ACS Catal. 2014, 4, 2917–2940. [Google Scholar] [CrossRef]
  3. Shimakawa, Y.; Azuma, M.; Ichikawa, N. Multiferroic Compounds with Double-Perovskite Structures. Materials 2011, 4, 153–168. [Google Scholar] [CrossRef]
  4. Mefford, J.T.; Hardin, W.G.; Dai, S.; Johnston, K.P.; Stevenson, K.J. Anion charge storage through oxygen intercalation in LaMnO3 perovskite pseudocapacitor electrodes. Nat. Mater. 2014, 13, 726–732. [Google Scholar] [CrossRef] [PubMed]
  5. Xu, J.J.; Xu, D.; Wang, Z.L.; Wang, H.G.; Zhang, L.L.; Zhang, X.B. Synthesis of Perovskite-Based Porous La0.75Sr0.25MnO3 Nanotubes as a Highly Efficient Electrocatalyst for Rechargeable Lithium Oxygen Batteries. Angew. Chem. Int. Ed. 2013, 52, 3887–3890. [Google Scholar] [CrossRef] [PubMed]
  6. Artem, M.; Marina, R.; Alexander, B.; Alexander, G. Nanocrystalline BaSnO3 as an Alternative Gas Sensor Material: Surface Reactivity and High Sensitivity to SO2. Materials 2015, 8, 6437–6454. [Google Scholar]
  7. Yang, W.; Zhang, R.D.; Chen, B.H.; Bion, N.; Duprez, D.; Hou, L.W.; Zhang, H.; Royer, S. Design of nanocrystalline mixed oxides with improved oxygen mobility: A simple non-aqueous route to nano-LaFeO3 and the consequences on the catalytic oxidation performances. Chem. Commun. 2013, 49, 4923–4925. [Google Scholar] [CrossRef] [PubMed]
  8. Xu, J.J.; Wang, Z.L.; Xu, D.; Meng, F.Z.; Zhang, X.B. 3D ordered macroporous LaFeO3 as efficient electrocatalyst for Li-O2 batteries with enhanced rate capability and cyclic performance. Energy Environ. Sci. 2014, 7, 2213–2219. [Google Scholar] [CrossRef]
  9. Wu, Z.L.; Li, M.J.; Overbury, S.H. On the structure dependence of CO oxidation over CeO2 nanocrystals with well-defined surface planes. J. Catal. 2012, 285, 61–73. [Google Scholar] [CrossRef]
  10. Zhu, L.L.; Huang, B.C.; Wang, W.H.; Wei, Z.L.; Ye, D.Q. Low-temperature SCR of NO with NH3 over CeO2 supported on modified activated carbon fibers. Catal. Commun. 2011, 12, 394–398. [Google Scholar] [CrossRef]
  11. Deng, W.J.; Chen, D.H.; Chen, L. Synthesis of monodisperse CeO2 hollow spheres with enhanced photocatalytic activity. Ceram. Int. 2015, 41, 11570–11575. [Google Scholar] [CrossRef]
  12. Xiang, X.P.; Zhao, L.H.; Teng, B.T.; Lang, J.J.; Hu, X.; Li, T.; Fang, Y.A.; Luo, M.F.; Lin, J.J. Catalytic combustion of methane on La1−xCexFeO3 oxides. Appl. Surf. Sci. 2013, 276, 328–332. [Google Scholar] [CrossRef]
  13. Stathopoulos, V.N.; Belessi, V.C.; Bakas, T.V.; Neophytides, S.G.; Costa, C.N.; Pomonis, P.J.; Efstathiou, A.M. Comparative study of La-Sr-Fe-O perovskite-type oxides prepared by ceramic and surfactant methods over the CH4 and H2 lean-deNOx. Appl. Catal. B 2009, 93, 1–11. [Google Scholar] [CrossRef]
  14. Shin, T.H.; Ida, S.; Ishihara, T. Doped CeO2-LaFeO3 Composite Oxide as an Active Anode for Direct Hydrocarbon-Type Solid Oxide Fuel Cells. J. Am. Chem. Soc. 2011, 133, 19399–19407. [Google Scholar] [CrossRef] [PubMed]
  15. Shikha, P.; Kang, T.S.; Randhawa, B.S. Effect of different synthetic routes on the structural, morphological and magnetic properties of Ce doped LaFeO3 nanoparticles. J. Alloy. Compd. 2015, 625, 336–345. [Google Scholar] [CrossRef]
  16. Sun, Y.; Hla, S.S.; Duffy, G.J.; Cousins, A.J.; French, D.; Morpeth, L.D.; Edwards, J.H.; Roberts, D.G. Effect of Ce on the structural features and catalytic properties of La(0.9−x)CexFeO3 perovskite-like catalysts for the high temperature water-gas shift reaction. Int. J. Hydrogen Energy 2011, 36, 79–86. [Google Scholar] [CrossRef]
  17. Liu, L.M.; Sun, K.N.; Li, X.K.; Zhang, M.; Liu, Y.B.; Zhang, N.Q.; Zhou, X.L. A novel doped CeO2-LaFeO3 composite oxide as both anode and cathode for solid oxide fuel cells. Int. J. Hydrogen Energy 2012, 37, 12574–12579. [Google Scholar] [CrossRef]
  18. Xia, Y.; Bernert, J.T. Stability of the Tobacco-Specific Nitrosamine 4-(Methylnitrosamino)-1-(3-Pyridyl)-1-Butanol in Urine Samples Stored at Various Temperatures. J. Anal. Toxicol. 2010, 34, 411–415. [Google Scholar] [CrossRef] [PubMed]
  19. Lin, W.G.; Zhou, Y.; Gu, F.N.; Zhou, S.L.; Zhu, J.H. Catalytic degradation of tobacco-specific nitrosamines by ferric zeolite. Appl. Catal. B 2013, 129, 301–308. [Google Scholar] [CrossRef]
  20. Jin, Z.H.; Gao, F.Q.; Flagg, T.; Deng, X.M. Nicotine induces multi-site phosphorylation of bad in association with suppression of apoptosis. J. Biol. Chem. 2004, 279, 23837–23844. [Google Scholar] [CrossRef] [PubMed]
  21. Wu, J.J.; Yang, T.; Li, X.; Xia, Y.; Zhao, Y.; Zou, F.; Jiang, Y.G. 4-(Methylnitrosamino)-1-(3-Pyridyl)-1-Butanone Induces Circulating MicroRNA Deregulation in Early Lung Carcinogenesis. Biomed. Environ. Sci. 2014, 27, 10–16. [Google Scholar] [PubMed]
  22. Shi, H.Z.; Wang, R.Y.; Bush, L.P.; Zhou, J.; Yang, H.J.; Fannin, N.; Bai, R.S. Changes in TSNA Contents during Tobacco Storage and the Effect of Temperature and Nitrate Level on TSNA Formation. J. Agric. Food Chem. 2013, 6, 11588–11594. [Google Scholar] [CrossRef] [PubMed]
  23. Li, Y.Y.; Wan, M.M.; Zhu, J.H. Cleaning carcinogenic nitrosamines with zeolites. Environ. Chem. Lett. 2014, 12, 139–152. [Google Scholar] [CrossRef]
  24. Deng, Q.X.; Huang, C.Z.; Zhang, J.P.; Xie, W.; Xu, H.C.; Wei, M.D. Selectively reduction of tobacco specific nitrosamines in cigarette smoke by use of nanostructural titanates. Nanoscale 2013, 5, 5519–5523. [Google Scholar] [CrossRef] [PubMed]
  25. Liu, X.M.; Gao, W.L.; Zhang, J. Facile synthesis of monodispersed CeO2 nanostructures. J. Phys. Chem. Solids 2011, 72, 1472–1476. [Google Scholar] [CrossRef]
  26. Kuo, D.H.; Huang, K.C. Characterizations of Gd(Fe1−xInx)O3 films prepared by chemical solution deposition. Electrochem. Solid State Lett. 2007, 10, 47–50. [Google Scholar] [CrossRef]
  27. Cullity, B.D.; Stock, S.R. Elements of X-ray Diffraction; Prentice Hall: Upper Saddle River, NJ, USA, 2001; pp. 385–433. [Google Scholar]
  28. Sun, X.M.; Li, Y.D. Colloidal carbon spheres and their core/shell structures with noble-metal nanoparticles. Angew. Chem. Int. Ed. 2004, 43, 597–601. [Google Scholar] [CrossRef] [PubMed]
  29. Wu, X.Y.; Niu, H.L.; Fu, S.S.; Song, J.M.; Mao, C.J.; Zhang, S.Y.; Zhang, D.W.; Chen, C.L. Core-shell CeO2@C nanospheres as enhanced anode materials for lithium ion batteries. J. Mater. Chem. A 2014, 2, 6790–6795. [Google Scholar] [CrossRef]
  30. Gallego, G.S.; Alzate, N.M.; Arnache, O. A novel LaFeO3−XNX oxynitride. Synthesis and characterization. J. Alloy. Compd. 2013, 549, 163–169. [Google Scholar] [CrossRef]
  31. Noroozifar, M.; Khorasani-Motlagh, M.; Ekrami-Kakhki, M.S.; Khaleghian-Moghadam, R. Enhanced electrocatalytic properties of Pt-chitosan nanocomposite for direct methanol fuel cell by LaFeO3 and carbon nanotube. J. Power Sources 2014, 248, 130–139. [Google Scholar] [CrossRef]
  32. Wang, Y.; Gong, L.; Li, Y.B.; Wei, Z.X. Combustion synthesis of La0.8Sr0.2MnO3 and its effect on HMX thermal decomposition. Chin. J. Chem. Eng. 2010, 18, 397–401. [Google Scholar] [CrossRef]
  33. Pinaeva, L.G.; Isupova, L.A.; Prosvirin, I.P.; Sadovskaya, E.M.; Danilova, I.G.; Ivanov, D.V.; Gerasimov, E.Y. La-Fe-O/CeO2 Based Composites as the Catalysts for High Temperature N2O Decomposition and CH4 Combustion. Catal. Lett. 2013, 143, 1294–1303. [Google Scholar] [CrossRef]
  34. Phokha, S.; Pinitsoontorn, S.; Maensiri, S.; Rujirawat, S. Structure, optical and magnetic properties of LaFeO3 nanoparticles prepared by polymerized complex method. J. Sol Gel Sci. Technol. 2014, 71, 333–341. [Google Scholar] [CrossRef]
  35. Kumar, R.D.; Jayavel, R. Facile hydrothermal synthesis and characterization of LaFeO3 nanospheres for visible light photocatalytic applications. J. Mater. Sci. Mater. Electron. 2014, 25, 3953–3961. [Google Scholar] [CrossRef]
  36. Concepcion, P.; Corma, A.; Silvestre-Albero, J.; Franco, V.; Chane-Ching, J.Y. Chemoselective hydrogenation catalysts: Pt on mesostructured CeO2 nanoparticles embedded within ultrathin layers of SiO2 binder. J. Am. Chem. Soc. 2004, 126, 5523–5532. [Google Scholar] [CrossRef] [PubMed]
  37. Wei, Z.X.; Xu, Y.Q.; Liu, H.Y.; Hu, C.W. Preparation and catalytic activities of LaFeO3 and Fe2O3 for HMX thermal decomposition. J. Hazard. Mater. 2009, 165, 1056–1061. [Google Scholar] [CrossRef] [PubMed]
  38. Yang, J.; Yang, J.Y.; Zhou, Y.; Wei, F.; Lin, W.G.; Zhu, J.H. Hierarchical functionalized MCM-22 zeolite for trapping tobacco specific nitrosamines (TSNAs) in solution. J. Hazard. Mater. 2010, 179, 1031–1036. [Google Scholar] [CrossRef] [PubMed]
  39. Lin, W.G.; Zhou, Y.; Cao, Y.; Zhou, S.L.; Wan, M.M.; Wang, Y.; Zhu, J.H. Applying heterogeneous catalysis to health care: In situ elimination of tobacco-specific nitrosamines (TSNAs) in smoke by molecular sieves. Catal. Today 2013, 212, 52–61. [Google Scholar] [CrossRef]
  40. Fu, S.S.; Niu, H.L.; Tao, Z.Y.; Song, J.M.; Mao, C.J.; Zhang, S.Y.; Chen, C.L.; Wang, D. Low temperature synthesis and photocatalytic property of perovskite-type LaCoO3 hollow spheres. J. Alloy. Compd. 2013, 576, 5–12. [Google Scholar] [CrossRef]
Materials 09 00326 g001 1024
Figure 1. (A) XRD spectra of different samples: (a) CeO2; (b) LaFeO3; (c) CeO2-LaFeO3 precursor; and (d) CeO2-LaFeO3; Inset: X-ray diffraction peak around 32° of LaFeO3 and CeO2-LaFeO3; (B) FT-IR spectra of: (a) CeCO3OH@C; (b) CeO2-LaFeO3 precursor; and (c) CeO2-LaFeO3; TG-DSC curves of (C) LaFeO3 precursor; (D) CeO2-LaFeO3 precursor.
Figure 1. (A) XRD spectra of different samples: (a) CeO2; (b) LaFeO3; (c) CeO2-LaFeO3 precursor; and (d) CeO2-LaFeO3; Inset: X-ray diffraction peak around 32° of LaFeO3 and CeO2-LaFeO3; (B) FT-IR spectra of: (a) CeCO3OH@C; (b) CeO2-LaFeO3 precursor; and (c) CeO2-LaFeO3; TG-DSC curves of (C) LaFeO3 precursor; (D) CeO2-LaFeO3 precursor.
Materials 09 00326 g001
Materials 09 00326 g002 1024
Figure 2. SEM and TEM images of (A,B) carbonaceous spheres; (C,D) CeCO3OH@C.
Figure 2. SEM and TEM images of (A,B) carbonaceous spheres; (C,D) CeCO3OH@C.
Materials 09 00326 g002
Materials 09 00326 g003a 1024Materials 09 00326 g003b 1024
Figure 3. SEM and TEM images of (A,B) LaFeO3; (C,D) CeO2; (E,F) CeO2-LaFeO3.
Figure 3. SEM and TEM images of (A,B) LaFeO3; (C,D) CeO2; (E,F) CeO2-LaFeO3.
Materials 09 00326 g003aMaterials 09 00326 g003b
Materials 09 00326 g004 1024
Figure 4. N2 adsorption and desorption isotherms of LaFeO3, CeO2 and CeO2-LaFeO3 composite.
Figure 4. N2 adsorption and desorption isotherms of LaFeO3, CeO2 and CeO2-LaFeO3 composite.
Materials 09 00326 g004
Materials 09 00326 g005 1024
Figure 5. XPS spectra of (A) La 3d; (B) Fe 2p; (C) Ce 3d; (D) O 1s for LaFeO3, CeO2 and CeO2-LaFeO3; (E) C 1s.
Figure 5. XPS spectra of (A) La 3d; (B) Fe 2p; (C) Ce 3d; (D) O 1s for LaFeO3, CeO2 and CeO2-LaFeO3; (E) C 1s.
Materials 09 00326 g005
Materials 09 00326 g006 1024
Figure 6. (A) Adsorbed and degradation percentage of NNK by CeO2, LaFeO3 and CeO2-LaFeO3; (B) The resonance structure of NNK; (C) The possible adsorption and catalytic rupture manner of NNK on CeO2-LaFeO3.
Figure 6. (A) Adsorbed and degradation percentage of NNK by CeO2, LaFeO3 and CeO2-LaFeO3; (B) The resonance structure of NNK; (C) The possible adsorption and catalytic rupture manner of NNK on CeO2-LaFeO3.
Materials 09 00326 g006
Materials 09 00326 sch001 1024
Scheme 1. Synthetic route to the CeO2-LaFeO3 perovskite composite.
Scheme 1. Synthetic route to the CeO2-LaFeO3 perovskite composite.
Materials 09 00326 sch001
Table
Table 1. Surface elemental composition/at % of as-prepared catalysts obtained from XPS.
Table 1. Surface elemental composition/at % of as-prepared catalysts obtained from XPS.
SamplesFeCeLaOC
CeO2-22.14-52.0125.85
LaFeO317.01-14.1951.617.2
CeO2-LaFeO313.589.310.149.4717.55

Share and Cite

MDPI and ACS Style

Wang, K.; Niu, H.; Chen, J.; Song, J.; Mao, C.; Zhang, S.; Zheng, S.; Liu, B.; Chen, C. Facile Synthesis of CeO2-LaFeO3 Perovskite Composite and Its Application for 4-(Methylnitrosamino)-1-(3-Pyridyl)-1-Butanone (NNK) Degradation. Materials 2016, 9, 326. https://doi.org/10.3390/ma9050326

AMA Style

Wang K, Niu H, Chen J, Song J, Mao C, Zhang S, Zheng S, Liu B, Chen C. Facile Synthesis of CeO2-LaFeO3 Perovskite Composite and Its Application for 4-(Methylnitrosamino)-1-(3-Pyridyl)-1-Butanone (NNK) Degradation. Materials. 2016; 9(5):326. https://doi.org/10.3390/ma9050326

Chicago/Turabian Style

Wang, Kaixuan, Helin Niu, Jingshuai Chen, Jiming Song, Changjie Mao, Shengyi Zhang, Saijing Zheng, Baizhan Liu, and Changle Chen. 2016. "Facile Synthesis of CeO2-LaFeO3 Perovskite Composite and Its Application for 4-(Methylnitrosamino)-1-(3-Pyridyl)-1-Butanone (NNK) Degradation" Materials 9, no. 5: 326. https://doi.org/10.3390/ma9050326

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop