Green Synthesis of Nanostructure CeO2 Using Tea Extract: Characterization and Adsorption of Dye from Aqueous Phase

Nanostructure CeO2 powders were synthesized using tea waste extract as gel precursor. The as-prepared samples were characterized by thermogravimetric analyzer (TGA), X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. Based on the TGA/DTG analysis, the intermediates of cerium chloride hydrates (CeCl3.4H2O and CeCl3.H2O) and cerium anhydrous (CeCl3) were produced, and the formation temperature of CeO2 was estimated to be 773 K. The cubic fluorite structure of CeO2 was detected to be the predominant species and was completely formed at the calcination temperature of 773K–1073 K with a crystal size between 8.8 and 11.4 nm based on the XRD measurement. Moreover, the main chemical state of ceria on the surface of the synthesized samples was confirmed to be tetravalent ceria by XPS. All samples show a strong Raman signal at a well-defined chemical shift of 463 cm−1 and a significant symmetry feature was observed, suggesting that the tetravalent ceria is the dominant species throughout the bulk sample. All the synthesized CeO2 calcined at different temperatures showed higher adsorption efficiency for Congo red (CR) compared with commercial CeO2. The adsorption efficiency maintained a steady state of more than 95% when the concentration of CR and adsorption temperature were varied in this study. The kinetic analysis showed that the second-order model was the appropriate model to interpret the adsorption behavior of synthesized CeO2. The calculated adsorption capacity derived from the second-order model is in good agreement with the experimental data. The isotherm analysis revealed that the Freundlich and D-R models fit well for the synthesized CeO2 and represent physisorption with a multilayer mechanism. The thermodynamic parameters, including the changes in Gibb's free energy, enthalpy, and entropy, suggested that the adsorption of CR on the synthesized CeO2 sample was a spontaneous and endothermic process.


Introduction
In recent decades, rare earth oxides have attracted the most attention because of their unfilled 4f electron structure, leading to extensive use in many fields. Among the rare earth oxides mentioned in industrial applications, cerium dioxide has received enormous attention because it can be used as luminescent materials [1], solid oxide fuel cells [2], and catalyst [3] and amperometric oxygen monitors [4]. It is undeniable that the synthesis, preparation, and application of CeO 2 will continue to be a popular topic in the future. Current methods for the synthesis of CeO 2 include chemical precipitation [4][5][6], hydrothermal process [7], sol-gel process [8], spray pyrolysis [9], microemulsion method [10], and electrochemical process [11]. Although these techniques are widely used for the synthesis of CeO 2 , they are complex, time-consuming, and involve a larger amount of hazardous chemicals, which drive up production costs and pose a serious threat to the environment and ecosystem. Moreover, they are inefficient due to higher cost, tedious downstream processing, lower biocompatibility, instability, and low yield [12][13][14]. erefore, it is necessary to develop a rapid, simple, inexpensive, and environmentally friendly synthesis method for CeO 2 . Currently, many efforts are being made to develop green synthesis by plants, microbes, and other biological derivatives. e use of plants or plant extracts as reducing and capping or stabilizing agents in the synthesis of nanostructured metals is more useful than other biosynthesis procedures [15]. In addition, cell culture and cell maintenance are not required during the process and the synthesized nanostructure products are more stable, have different shapes and sizes for specific applications, and are inexpensive [16][17][18]. In recent years, more than thirty plant species have been used for the synthesis of nanostructured CeO 2 , including orange peel, walnut shell, olive leaf, aloe vera leaf, Prosopis juliflora, Jatropha curcas, and Elaeagnus angustifolia [19][20][21][22][23][24][25]. ese reports suggest that the synthesis of nanostructured CeO 2 is still a hot topic.
Congo red (CR) is a benzidine-based anionic diazo dye and is widely used in the textile, paper, and plastic industries. It is reported that the theoretical size of CR is 2.29 nm * 0.82 nm * 0.60 nm based on the Gaussian calculation, which is larger than methylene blue and methylene orange [26]. Another feature of CR is that the size of CR aggregates is up to 40 nm when the concentration is 1 mmol/ L [27]. ese characteristics make Congo red more difficult to remove compared with other dyes. Table 1 shows the common technologies used to remove CR such as adsorption, photocatalytic degradation, Fenton-like reaction, and sonocatalytic degradation. Although most of them achieve superior removal efficiency, there are some drawbacks such as high energy requirement and cost for photocatalytic and sonocatalytic degradation and additional chemical reagent requirement for Fenton-like reaction, which lead to a development limitation for the removal of CR. erefore, adsorption treatment is considered one of the most efficient and convenient methods for removing CR from aqueous solutions.
Tea is one of the most important agricultural products in China and a popular staple food in many Asian countries. Unlike other beverages, most tea is discarded after brewing, causing tea waste to become a serious environmental problem if not treated properly. To solve this problem, many technologies have been developed to reuse tea waste. e most popular use of tea waste is as an adsorbent to remove heavy metals and dyes from aqueous systems. Celesi et al. studied the removal of heavy metal ions (Pb, Cd, Ni, and Zn) using brewed tea waste. e highest efficiency was in the order of Pb (98%)> Cd (85%)>Ni (82%)>Zn (76%) [38]. Nigam et al. showed that the tea waste can remove 71% of total solids, 55% of TDS, and 74.8% of COD from tannery industry wastewater besides significantly high removal of Cr, and the tea waste can be reused up to 5 cycles [39]. In addition to the raw material, the modified tea waste is also widely used. Wen et al. prepared a composite with iron oxide nanoparticle from tea waste for the removal of Cu and Zn, and achieved high adsorption capacities of 95.44 and 68.78 mg/g, respectively [40]. Our studies have shown that the tea waste stem, oolong tea, and black tea have high adsorption capacity of 103.09, 302.63, and 312.50 mg/g for methylene blue, respectively [41][42][43].
is interpretation suggests that the tea waste and tea-based adsorbents are quite effective in removing pollutants from aqueous systems.
It is well known that tea wastes contain considerable reductive chemical substances such as polyphenols, thearubigins, theaflavins, and theabrownins. ese reductive chemical substances are potential candidates for chelation with metals to form a gel-metal precursor, and nanoscale metal oxides are synthesized after the calcination process. From this viewpoint, the reductive chemical substances can be extracted from the tea wastes to be used for the synthesis of nanometals and the remaining tea wastes are further used as adsorbents for the removal of pollutants from the aqueous or gaseous state. is indeed represents a new aspect of tea waste reuse and is an acceptable treatment to create value for tea waste.
As far as we know, the use of the extract obtained from tea waste for the synthesis of nano-CeO 2 has not been addressed in previous reports. erefore, the main objective of this study was to prove the feasibility of synthesizing nano-CeO 2 and evaluate its properties by TGA, XRD, XPS, SEM, and Raman spectroscopy. Moreover, the synthesized CeO 2 is used to test its ability to adsorb Congo red from aqueous solution and a series of kinetic models, isotherm equations, and thermodynamics are carried out to understand the nature of adsorption. e purpose of this study was to gain a better understanding of the new synthetic method for the preparation of nano-CeO 2 and its application.

Preparation of Tea Waste and Synthesis
Procedure for CeO 2 . Tea waste was collected from the local tea market, Anxi County, Fujian Province. e tea waste samples were pretreated with distilled water to remove unwanted and uncleaned materials present on the surface of the tea waste. e tea waste samples were dried at room temperature for 24 hours and stored in a thermostat. To obtain the extract of tea waste, five grams of tea waste was weighed and mixed with 100 mL of distilled water in a 250 mL beaker. e mixed solution was treated with a 100 rpm for 60 min at 353 K. After cooling, the extract solution was centrifuged at 5000 rpm for 5 min and filtered using a Hirsch funnel to obtain a pure extract of tea waste. To prepare the cerium precursor, 0.05 mol cerium chloride was added to a 20 mL of extract solution and continuously stirred for 12 hours using a magnetic stirrer. After stirring, the gel-cerium precursor was formed and dried at 393 K for 24 hours in an oven. e dried gel-cerium samples were calcined at different temperatures under air atmosphere.

Characteristic of Synthesized CeO2
2.2.1. TGA/DTG Analysis for Weight Loss. Weight loss as a function of temperature for gel-cerium precursor was performed by a thermogravimetric analysis equipped with differential thermal analysis (TGA/DTG, Perkin Elmer Pyris Diamond Model). An amount of 50 mg of gel-cerium precursor was heated in dry air atmosphere to 1073 K with a heating rate of 10°C/min.

X-Ray Diffraction Analysis for Crystalline Structure.
e crystalline structures of the synthesized CeO 2 samples after different calcination processes were determined by X-ray powder diffraction (RIGAKU Model D/MAX III-V) with CuKα radiation. e applied current and voltage were 30 mA and 40 kV, respectively. Diffraction patterns were recorded in the angle range 2θ � 10-65°at a scan rate of 3°/min.

BET Surface Evaluation.
e surface area was measured by adsorption of nitrogen at 77 K using a Micromeritics ASAP 2010 Instrument. Prior to the adsorption measurements, the samples were degassed under vacuum conditions (5 μm Hg) at 373 K for 2 hours. e surface area was calculated by the BET equation.

X-Ray Photoelectron Spectroscopy (XPS).
e surface composition of the synthesized CeO 2 sample was measured using a VG Micro Lab. MKIII XPS analyzing instrument with an Mg Kα X-ray radiation source (1253.6 eV). e pressure in the vacuum chamber was maintained at 1.33 × 10 −10 kPa using an ion pump. e analysis condition was a resolution of 0.1 eV; the number of scans was 100. e binding energy spectra were obtained under the abovementioned conditions and a predetermined scan range.

Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM).
e morphology of the synthesized CeO 2 samples was observed by scanning electron microscopy (Philips XL40 FE-SEM). e transmission electron microscopy (TEM) images were performed with a Hitachi 800 with an accelerating voltage of 200 kV.
2.2.6. Raman Spectroscopy. Raman spectra were recorded at room temperature in a wavelength range of 200-1200 cm −1 with the spectral resolution of 10 cm −1 using a LabRam type Raman spectrometer (Jobin Yvon). A He-Ne laser was used as the exciting source.

Batch Experiment for CR Adsorption.
e adsorption activity of the synthesized CeO 2 for Congo red (CR) was determined in a batch experiment. For comparison, a commercial pure CeO 2 was experimentally evaluated under identical conditions. All adsorption experiments were carried in a conical flask with a concentration of 100 mg/L and 25 mL of the CR solution. A certain weight of 0.25 g sample and CR solution was placed on a thermal-controlled shaker for 60 min at a sharking rate of 200 rpm. After the adsorption experiment, the solution was centrifuged at 5000 rpm for 10 minutes and the supernatant solution was analyzed to determine the concentration of CR by UV-visible spectrophotometer at 496 nm.

Isotherm and Kinetic Investigations.
e Langmuir model is widely used to represent the adsorption of a monolayer that has reacted on the surface of CeO 2 . e Langmuir model can be expressed as follows: where C e and C 0 (mg/L) are the concentration of CR at the equilibrium and initial phases, respectively. Q m (mg/g) is the maximum adsorption capacity, and Q e (mg/g) is the adsorption capacity of the equilibrium phase. e dimensionless equilibrium parameter R L estimates whether the Langmuir isotherm is favorable. When 0 < R L < 1, the adsorption process is generally considered favorable, while unfavorable is when R L > 1, as well as R L � 1 means that the adsorption process is linear; when R L � 0, the adsorption is irreversible.
e Freundlich model is used to describe the multilayer adsorption of CR molecules on the heterogeneous surface of cerium materials. e equation can be represented as follows: where K F is the Freundlich constant and n is the heterogeneity factor. e value of 1/n less than 1 indicates that the interaction between CR molecules and CeO 2 is favorable.  [37] e Dubinin-Radushkevich model (D-R) is applicable to the adsorption of CR on both homogeneous and heterogeneous surfaces. e linear equation can be represented as follows: where Q e and Q D-R are the amount of CR adsorbed at equilibrium (mg/g) and the theoretical capacity of CeO 2 (mg/g). ε is the Polanyi potential. β is related to the mean free energy (E) (kJ/mol) of adsorption per mole of CR. e Temkin model assumes that the heat of adsorption of the molecules in the layer decreases linearly with coverage due to adsorbent-adsorbate interactions and mainly describes the chemisorption process dominated by electrostatic adsorption. e linear form is expressed as follows: where B T (J/mol) is the Temkin constant and A T (L/mg) denotes the equilibrium binding constant of the Temkin isotherm.
In this study, the first-order and second-order kinetic models were applied to investigate the adsorption process. e first-order kinetic model was proposed by Lagergren, and it was based on physical adsorption. It is assumed that the adsorption rate is proportional to the change in saturation concentration and adsorption capacities. is linear form of the model can be expressed as follows: where Q e and Q t are the adsorption capacities (mg/g) at the equilibrium phase and at any time t, respectively. K 1 (1/min) is the constant rate. e second-order kinetic model is widely used to illustrate the limiting rate chemical adsorption process. e model is expressed as follows: where Q e and Q t are the amounts of CR concentration and K 2 (g/mg/min) is the constant rate of the second-order kinetic model.

TGA/DTG Measurement.
To understand the formation temperature of nanostructure CeO 2 synthesized from tea extract and cerium precursor, the synthesized sol-gel-cerium sample was measured by TGA/DTG in the airflow and the profile is shown in Figure 1. Four stages of weight loss are observed in Figure 1. e profile of DTG agreed with the result reported by Xue et al. in which their research showed the identical trend and proposed a stepwise dehydration mechanism of CeCl 3 .7H 2 O [44]. ey proposed that the dehydration mechanism of CeCl 3 .7H 2 O followed the reaction of CeCl 3 .7H 2 O to CeCl 3 .4H 2 O, and to CeCl 3 .H 2 O and CeCl 3 . e final product was CeO 2 at a temperature of 863 K. As shown in Figure 1, a large weight loss was found at 773 K, which was attributed to the formation of CeO 2 through the oxidation reaction of CeCl 3 . Note that the formation temperature of CeO 2 in this study is much lower than that of Xue et al. [44]. e redox potential of cerium decreases with pH value, which causes the Ce(III) to be easily oxidized to Ce(IV) at the weaker acidity. e pH value of the tea extract used in this study is determined to be ±6.5 providing another favorable driving force for the oxidation of Ce(III) to Ce(IV). In particular, the formation temperature of CeO 2 can be reached at about 773 K, which reduces the energy consumption and the use of chemical reagents for the synthesis of metal oxides.

XRD Analysis.
XRD identification was evaluated to verify the finding and decomposition behavior of gel-cerium from the TGA. Figure 2 shows the phase transformation of dried gel-cerium sample in the temperature range of 298 K-1073 K. e dried gel-cerium sample shows disordered crystal phases, mainly consisting of CeCl 3 .7H 2 O, CeCl 3 .4H 2 O, and CeCl 3 .3H 2 O, accompanied by unidentified crystal phases. e unidentified crystal phases probably originate chelation and complexation between tea polyphenols and other organic matters during the sol-gel process.
e unidentified crystal phases disappear with temperature, and the CeCl 3 is the main species at 573 K. All the crystal water is decomposed at this stage. It is noteworthy that the tiny crystal peak of CeO 2 is first detected at 673 K and the well-crystalline CeO 2 phase is observed at 773 K-1073 K. e 2θ values were located at 28.5, 33.1, 47.5, is result is corresponding with the TGA measurement, and it is concluded that the formation temperature of CeO 2 in this study is approximately 773 K. e crystalline size of CeO 2 at different heat treatments was estimated using the Scherrer equation: where λ is the X-ray wavelength (0.154 nm), β is the full width of the diffraction line at half of the maximum intensity, and θ is the half diffraction angle. e calculated results are summarized in Table 2. e crystalline size of CeO 2 increased with temperature. e crystalline size synthesized in this study ranged from 8.8 to 11.4 nm, which is similar to some synthesis reports [45][46][47][48]. Table 3 shows the comparison of CeO 2 crystal size calculated using the Scherrer equation. As shown, the crystal size of 8.8-11.4 nm is relatively small for all samples, indicating that the tea extract is an acceptable and potential substrate to synthesize the nanostructure CeO 2 . e difference in particle size could be due to the difference in the relaxation of particle surface. In this study, tea polyphenol and large amounts of other substances such as amino acid, theaflavin, and thearubigin are important components of tea extract. During the experimental procedure, the cream-like gel can be easily  Bioinorganic Chemistry and Applications formed due to the interaction between tea polyphenol, amino acid, theaflavin, and thearubigin. It is believed that the formation of the cream-like gel stabilizes the small particles and reduces the surface relaxation of the forming nanoparticles resulting in smaller lattice parameters. Moreover, note that the lattice parameter decreases with crystalline size and is lower than that reported for CeO 2 in the standard data JCPDS 34-0349. is result is also in agreement with those of Leoni and Maensiri et al., in which their investigations demonstrated that the lattice parameter of nanocrystalline CeO 2 is a function of calcination temperature [55,56]. For nanocrystalline particles, the lattice parameter is found to vary with particle size and can be explained by the relaxation of the grain surface. It is supported that the nanocrystalline particles have a core-shell structure and the core structure is very close to that of bulk monocrystalline cerium oxide. e lattice parameter increases locally at the surface due to the surface trends to relax. In addition, the grain surface relaxation was found to contribute to the line broadening and thus tends to reduce the measured value of dislocation density [57]. Figure 3 shows SEM and TEM images of the synthesized samples obtained at different heat treatments in air atmosphere. A smooth and flat surface of the gel-Ce sample is obviously observed, and the formation of a prism-like shape seems to have been observed at 723 K. Meanwhile, the distinct hexahedral shape of CeO 2 is formed, which is accompanied by irregular shape and agglomeration. In particular, at 1073 K, a larger amount of homogeneous structure of CeO 2 with spherical shape and hexahedral trace shape is obtained. It is reported that the morphology, such as crystal size and physiochemical properties of cerium oxide, can be easily controlled using hydroxycarbonates as precursors. e change in shape from prismatic to spherical is attributed to the high content of hydroxycarbonates in tea extract. At high temperatures, CO 3 2combined with the positively charged groups to form the solid CeCO 3 OH at supersaturation and the phase transformation of CeCO 3 OH to CeO 2 after heat treatment [58,59].

SEM and TEM Observation.
e TEM image of synthesized CeO 2 shows that the sphere has a diameter of about 190 nm. is result is similar to the research report by Zhou et al., in which spherical CeO 2 crystallites composed of nanoparticles were synthesized by hydrothermal treatment because small CeO 2 nanoparticles aggregated and gradually evolved into a spherical structure with a low surface energy [60]. As can be seen in Figure 3(f ), the value of d-space is about 0.31 nm, which corresponds to the (111) lattice plane of CeO 2 . is is in good agreement with the results obtained from XRD and standard data (JCPDS 34-0394). From the SEM observation, the presence of particles is well-defined and the agglomeration property between the particles was also found at the temperature range of 723K-1073 K. Agglomeration is a commonly occurring feature because particles tend to decrease the exposed surface area to lower the surface energy. When two particles are in contact, due to the existence of mismatch between the lattices, the two crystals tend to rotate with each other to minimize the interfacial strain energy. erefore, the same types of crystal planes tend to align with each other, forming a coherent interface to reduce the interfacial energy [60][61][62].

XPS Determination.
To examine the chemical state and valence of cerium, the XPS was used to survey the surface composition of the test samples and the spectra of Ce 3d are shown in Figure 4. Typically, the Ce 3d XPS core-level spectra exhibit three spin-orbit doublet features (around 879-890 eV, 895-910 eV, and around 916 eV). In general, it consists of six peaks, corresponding to the pairs of spin-orbit doublets, which can be attributed to the presence of Ce 3d 5/2 and Ce 3d 3/2 . As depicted in Figure 4, the labeled v and u correspond to the structure of Ce 3d 5/2 and Ce 3d 3/2 , respectively [63,64]. e highest binding energy peaks, v′′′ and u′′′, result from a Ce 3 d 9 O 2p 6 Ce 4f 0 final states. e lowest binding energy peaks, v′, v′′, u′, and u′′, are contributed by CeO 2 and result from a mixture of Ce 3 d 9 O 2p 5   [65]. Note that the satellite peak u′′′ associated with the Ce 3d 3/2 is characteristic of the presence of tetravalent Ce (Ce 4+ ions) in Ce compounds [63]. For all samples shown in Figure 4, the presence of three spin-orbit doublets (six peaks with satellite peak at 916.5 eV) demonstrated that the Ce (IV) is the predominant species. Figure 5 shows the Raman spectra of commercial CeO 2 and synthesized CeO 2 samples calcined at different temperatures. For all samples, a strong peak located at about 463 cm −1 is assigned to the F 2g Raman active mode of the cubic fluorite structure of CeO 2 , which is attributed to a symmetric stretching mode of the Ce-O 8 vibrational unit and the molecule maintains its tetrahedral symmetry throughout [66,67]. erefore, this mode should be very sensitive to any disorder in the oxygen sub-lattice resulting from thermal, doping, or grain size-induced effects. Apart from the sharp peak, no other peaks were detected in the Raman spectra. According to the previous investigations, the detectable Raman peaks were measured at about 260 cm −1 , 570 cm −1 , 1047 cm −1 , and 1170 cm −1 , respectively. e presence of 260 cm −1 represents the disorder in the system, while the peak at 570 cm −1 is assigned to the defect spaces containing oxygen vacancies [68,69]. Moreover, the peak centered 570 cm −1 can also be probably attributed to the presence of Ce 3+ [69]. e symmetric characteristic for the synthesized CeO 2 prepared by calcination at different temperatures appeared to have the same property. No asymmetric characteristic is observed for all samples. It is proposed that, when there is disorder in the oxygen sublattice, the Raman active mode is affected by a broadening of the line and an increase in its asymmetry, which is attributed to a decrease in phonon lifetime in the nanocrystalline regime [70,71]. Based on the XPS and Raman spectroscopic study, it is concluded that the synthesized CeO 2 derived from the tea extract is more stable and has a relatively ordered structure due to the presence of Ce 4+ .

Adsorption Evaluation for Congo Red (CR).
For a better understanding of the activity and performance on the adsorption of dye from aqueous solution, a series of synthesized CeO 2 and a commercial sample were considered for the adsorption of CR due to its carcinogenicity. Figure 6 shows the adsorption efficiency of CR by a commercial and synthesized CeO 2 sample calcined at different temperatures. A rapid increase in adsorption efficiency can be found within 5 minutes for all synthesized CeO 2 , implying the excellent reactivity between synthesized CeO 2 and CR. On the other hand, the adsorption efficiency seems to increase gradually and maintains a steady state for around 30 minutes. is is probably due to the presence of stronger mass transfer resistance between the commercial CeO 2 and the aqueous CR solution. Note that the color change for all CeO 2 samples after 1 min treatment shows an extreme difference in Figure 6(b). As shown, the color of CR solution adsorbed by all synthesized CeO 2 samples derived from tea extract shows a much distinct feature than the commercial CeO 2 , indicating that the adsorption reaction is exactly rapid for the synthesized CeO 2 samples. e adsorption efficiency is more than 95% for all synthesized CeO 2 samples, while it is only 41% for a commercial sample when the contact time was set to 1 min. e adsorption efficiency of the synthesized CeO 2 is more than two times higher than that of the commercial sample. e plausible reasons are (i) the greater surface area of synthesized CeO 2 . e surface area of synthesized CeO 2 and commercial CeO 2 is 33.66 m 2 /g and 6.23 m 2 /g, respectively. It is expected that the larger surface area favors the adsorption process and leads to the better adsorption efficiency of CR for synthesized CeO 2 . (ii) e better dispersion of CeO 2 for the synthesized sample: to understand the dispersion of CeO 2 on the surface, the CO 2 temperature-programmed desorption (CO 2 -TPD) was employed. e desorbed amount of CO 2 at 400°C for synthesized CeO 2 was estimated to be 61.6 μmol-CO 2 /g, while it was 12.5μmol-CO 2 /g for  commercial CeO 2 . is result is an important finding that supports the adsorption experiment for the removal of CR. e larger desorbed amount of CO 2 indicates a better dispersion of CeO 2 on the surface. From the above results, it can be concluded that the synthesized CeO 2 from tea waste has better adsorption behavior, which can be contributed to the better dispersion of CeO 2 on the surface compared with the commercial CeO 2 .

Effect of Initial CR Concentration.
e effect of the initial CR concentration on the adsorption of CR at 298 K with a dosage of 10 g/L and a contact time of 60 min was investigated. As can be seen in Figure 7, the adsorption efficiency of all synthesized CeO 2 samples maintains a steady state in the range of 96%-98% and no deactivation feature is observed within the experimental conditions. e adsorption efficiency is as high as approximately 98% even at 800 mg/L. For a commercial CeO 2 , the adsorption efficiency is more than 85% when the CR concentration is between 100 and 300 mg/L and decreases to 70% at 600 mg/L, while the worst performance is observed at 800 mg/L. Based on the experimental results, it is suggested that the synthesized CeO 2 has a greater chemical affinity with CR than the commercial sample and is likely associated with multilayer adsorption mechanism with CR. Moreover, the synthesized CeO 2 samples showed better adsorption efficiency, which is attributed to the uniform dispersion of CeO 2 active sites throughout the bulk sample, thus promoting the overall adsorption efficiency even when the CR concentration was set to 800 mg/L. e ANOVA shows that the p value is much smaller than 0.01 (p value is 5.21 * 10 −8 ) for the concentration of CR, implying very significant differences between the adsorption efficiency and the concentration of CR.

Effect of Reaction
Temperature. e effect of temperature in the range of 278 K-318 K on the adsorption of CR with a dosage of 10 g/L and a contact time of 60 min was investigated. As shown in Figure 8, it was found that the adsorption efficiency maintains about 97% and does not change significantly in the range of 278 K-318 K for all synthesized CeO 2 , which can be explained by the fact that temperature is not a key factor to govern the overall reaction. e heat of reaction between the synthesized CeO 2 and CR would reach the steady state under the experimental conditions. Unlike synthesized CeO 2 , the adsorption efficiency of commercial CeO 2 decreased gradually with temperature, which can be explained by the fact that higher temperature may cause the desorption rate to be more favorable than that of adsorption, resulting in the release of part of the adsorbed CR from the solid phase to the liquid phase, thus decreasing the adsorption efficiency. Based on the experimental results, it is believed that the synthesized CeO 2 can be used in the temperature range of 278 K-318 K under the experimental conditions in this study. e ANOVA shows that the p value is much smaller than 0.01 (p value is 7.54 * 10 −11 ) for the reaction temperature, implying very significant differences between the adsorption efficiency and the reaction temperature in this study.

Study of Adsorption Kinetic.
Adsorption kinetics provides valuable information on the adsorption rate and relevant coefficients for pilot scale and engineering design. e first-order and second-order kinetic models were applied to fit the adsorption reaction and to investigate the nature of the process. e fitting results of the two models are summarized in Table 4. e correlation coefficient values (R 2 ) of the second-order model for synthesized and commercial CeO 2 are much better than those of the first-order model. Meanwhile, the fitted adsorption capacities (Q fit ) of synthesized and commercial CeO 2 derived from the secondorder model are estimated to be 9.5 mg/g and 4.07 mg/g, which is close to the experimental result (Q exp ) in this study.
ese results support that the second-order kinetic model is more suitable for understanding the adsorption process between CeO 2 and CR. e well-fitting result for secondorder model demonstrates that the rate-limiting step is not the resistance of the boundary layer [72]. e adsorption process is controlled by chemisorption, which involves valence forces due to the sharing or exchange of electrons between the adsorbent and the adsorbate [73,74]. e second-order model includes the external liquid film diffusion, intraparticle diffusion, and adsorption on the surface of the adsorbent; this model provides a more comprehensive and accurate description of the adsorption mechanism between powder CeO 2 and CR [75,76].

Adsorption Isotherm Models.
e fitting results and parameters of four isotherm models are listed in Table 5. For the synthesized CeO 2 , with the exception of the Langmuir model, the higher R 2 values were found in the range of 0.93-0.97 for other models. is suggested that the Langmuir model is not suitable to describe the interaction between synthesized CeO 2 and CR. e Freundlich model shows the best fitting result among all the models, indicating that the multilayer adsorption is the main mechanism, leading to rapid reaction and greater adsorption efficiency within the short contact time. However, the high value of R 2 derived from the Langmuir model for the commercial CeO 2 indicated that the interaction between the commercial CeO 2 and CR may be attributed to the monolayer adsorption, thus leading to the gradual increase in adsorption efficiency with contact time. In addition, the D-R model shows the superior R 2 values for both synthesized CeO 2 and commercial CeO 2 . e mean free energy (E) derived from D-R model was 0.32 kJ/mol and 0.11 kJ/mol for the synthesized and commercial CeO 2 , respectively, which is classified as the physisorption interaction. Moreover, the Temkin model also shows the high R 2 value for both synthesized CeO 2 and commercial CeO 2 , which implies that the electrostatic interaction probably is one of the mechanisms between CeO 2 and CR. By comparing the values of R 2 of the examined four isotherm models, it is concluded that the D-R and Temkin models fit well for both synthesized CeO 2 and commercial CeO 2 , and the Langmuir model is suitable for commercial CeO 2 , while the Freundlich model is the best model for the synthesized CeO 2 in this study.

3.11.
ermodynamics Investigation. To determine the thermodynamic parameters for the adsorption of CR by synthesized CeO 2 , experiments were conducted at 278 K, 288 K, 298 K, 303 K, and 318 K using a 100 mg/L of CR solution. e Gibbs free energy, ΔH 0 , and ΔS 0 were calculated, and the expression is as follows: where k is the rate constant related to the equilibrium phase. ΔH 0 and ΔS 0 are the enthalpy and entropy, respectively. T (K) is the absolute temperature, and R (8.314 J/mol/K) is the gas constant. e calculated parameters are shown in Table 6. e ΔG values are −7.49, −7.68, −8.31, −7.93, and −8.83, respectively, indicating that the adsorption of CR by synthesized CeO 2 is a spontaneous reaction. e values of ΔH 0 and ΔS 0 are 0.002 kJ/mol and 0.032 kJ/mol/K, respectively. erefore, the adsorption process can be assumed to be an endothermic reaction with the increase in the degree of disorder. e analysis of thermodynamics is similar to the fitting results of kinetic model.

Comparison of Other Adsorbents for CR Removal.
e comparison of the maximum adsorption capacity of CeO 2 for CR with that of other adsorbents in the literature is shown in Table 7.
e CeO 2 samples show comparable adsorption capacity for CR as compared to the adsorbents.

Conclusion
is study reported the synthesis of nanostructure CeO 2 powder using extract obtained from tea waste. e synthesized CeO 2 samples were characterized by thermogravimetric analyzer (TGA), X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy.
From the TGA/DTG analysis, the intermediate of cerium chloride hydrates such as CeCl 3 .4H 2 O and CeCl 3 .H 2 O and CeCl 3 was produced and it was proposed that the formation temperature of CeO 2 was estimated to be 773−K. e cubic fluorite structure of CeO 2 was detected to be the predominant species and was completely formed at the calcination temperature of 773 K-1073 K with a crystal size between 8.8 and 11.4 nm based on the XRD measurement. Moreover, the main chemical state of ceria on the surface of the synthesized samples was confirmed to be tetravalent ceria by XPS. All the samples show a strong Raman signal at a well-defined chemical shift at about 463 cm −1 and a significant symmetry feature was observed, inferring that the tetravalent ceria is the dominant species throughout the bulk sample. Except for commercial CeO 2 , a rapid increase in adsorption efficiency for all synthesized samples indicated better reactivity between synthesized CeO 2 and CR. e larger surface area and uniform dispersion of CeO 2 on the surface could be the main reason for the difference in adsorption efficiency of synthesized and commercial samples. For all synthesized CeO 2 samples, there is no difference in adsorption efficiency even when the concentration of CR was controlled to 800 mg/L. e adsorption efficiency was still more than 95%, while a distinct decrease was observed in the commercial sample. e same trend is reflected in the effect of reaction temperature. From the kinetic analysis and isothermal fitting, the second-order model was found to be the appropriate model to interpret the adsorption behavior of synthesized CeO 2 . e calculated adsorption capacity derived from the second-order model agreed well with the experimental data. e isothermal fitting results indicated that the Langmuir model is suitable for commercial CeO 2 , where the adsorption mechanism is dominated by a monolayer, while the Freundlich model is the best model for the synthesized CeO 2 in this study.
is also provided a useful explanation that the synthesized CeO 2 is better than the commercial sample as multiple layer adsorption of CR is possible for synthesized CeO 2 . ermodynamic investigation indicated that the adsorption mechanism between synthesized CeO 2 and CR was a spontaneous and endothermic process with the increase in the degree of disorder. In conclusion, the extract of tea waste is a readily available and environmentally friendly raw material for the synthesis of nanostructure CeO 2 .
Data Availability e data generated and analyzed in this manuscript are available from the corresponding author on reasonable request.

Conflicts of Interest
e authors declare that there are no conflicts of interest regarding the publication of this study.