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Efficient production of 5-hydroxymethylfurfural from fructose over CuAPO-5 molecular sieves synthesized using an ionothermal method

Yan Huang abc, Pilan Zhanga, Hualei Hu*a, Danxin Hua, Jie Yanga, Yexin Zhanga, Chunlin Chena, Yong Yanga, Jian Zhang*a and Lei Wang*a
aNingbo Institute of Materials Technology & Engineering, Chinese Academy of Sciences, 1219 Zhongguan West Road, Ningbo 315201, China. E-mail: huhualei@nimte.ac.cn; jzhang@nimte.ac.cn; wanglei@nimte.ac.cn
bShanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China
cUniversity of Chinese Academy of Sciences, Beijing 100049, China

Received 9th September 2019 , Accepted 11th October 2019

First published on 15th October 2019


Abstract

A group of CuAPO-5 molecular sieves with trace Cu were successfully synthesized via an ionothermal method and used for fructose dehydration to 5-hydroxymethylfurfural (HMF) in [BMIM]Br ionic liquid. The 0.06-CuAPO-5 sample displayed excellent performance and a HMF yield of 93.8% was obtained, which could be ascribed to the balance between acid strength and mass transfer efficiency. This work demonstrates that the ionothermal synthesized CuAPO-5 molecular sieve was also a good candidate for the efficient production of HMF.


1. Introduction

Renewable biomass conversion to useful chemicals has attracted rapidly increasing attention due to the gradual depletion of fossil energy resources.1 5-Hydroxymethylfurfural (HMF), one of the top platform chemicals based on green chemistry by USDOE in 2010, can be upgraded to produce a wide range of valuable derivatives such as 2,5-furandicarboxylic acid, 2,5-dimethylfuran, and 2,5-bis(hydroxymethyl)furan.2–4 Among the present synthesis routes to HMF, fructose dehydration is the most efficient and selective one to allow the large-scale production in the near future. Many efforts have been taken to develop a high-performance catalyst for this reaction, but the highly selective production of HMF is still a big challenge due to complicated side reactions.5,6

Solid acid catalysts (especially molecular sieves) offer many advantages including easy catalyst separation, less corrosion and controllable surface acidity.7–9 Recently, many aluminosilicate molecular sieves with different structures (MOR, BEA, LTL, etc.) have been used in the dehydration of fructose, exhibiting excellent catalytic performance (Fig. 1).10,11 As another important molecular sieves, metal substituted aluminophosphate molecular sieves (MAPO) have been broadly exploited in catalysis due to their good thermostability and modifiable acidity.12,13 However, only few works have been done on the use of MAPO in the HMF synthesis so far. For instance, several MeSAPO molecular sieves were produced via the hydrothermal method and catalyzed fructose dehydration in a biphasic system at 170 °C to obtain no more than 79% yield of HMF.14,15 This unsatisfied HMF yield was inconsistent with the excellent performance of MAPO catalysts in other acid-catalyzed dehydration reaction.16 Therefore, more fundamental researches should be conducted on the synthesis and catalytic role of MAPO to provide a new choice for HMF production.


image file: c9ra07217a-f1.tif
Fig. 1 Conversion of fructose over the solid acid catalysts.

Ionothermal method is a novel synthetic choice for the preparation of molecular sieves, where an ionic liquid can serve as the reaction solvent and also the structure directing agent (SDA) during the reaction process.17 The main advantage of ionothermal method is the removal of competition between the solvent and SDA for interaction with the growing crystal surface.18 In addition, the ionothermal reaction can take place at or near ambient pressure because of the negligible vapor pressure of ionic liquids.19 This eliminates the safety concerns associated with high pressures, which is a troublesome problem in the conventional hydrothermal process.20 Several types of MAPO materials (including SAPO, CoAPO, MgAPO, and FeAPO) have been successfully prepared via the ionothermal method.21–24

In this work, we report the synthesis of CuAPO-5 molecular sieves by ionothermal method and their utilization in the dehydration of fructose to HMF in ionic liquid. The 1-butyl-3-methylimidazolium bromide ([BMIM]Br) ionic liquid was chosen as the reaction media for both catalyst synthesis and the dehydration reaction. CuAPO-5 possesses an AFI structure and 12-membered ring pores (7.3 Å in size), while Cu atoms are quite difficult to incorporate into the AFI framework, resulting in much fewer successful examples than other MAPOs.25 CuAPO-5 was usually used to catalyze the selective reduction of NOx or oxidation of aromatic amines due to its redox property of Cu,26,27 and, to the best of our knowledge, there is no report on its application in the acid-catalyzed reactions.

2. Experimental

2.1. Materials

Tetraethylammonium hydroxide (TEAOH, 25%), aluminium isopropoxide (AIP, 99.99%), hydrofluoric acid (HF, 40%), fructose (99%) and 5-hydroxymethylfurfural (HMF, 99%) were purchased from Aladdin Industrial Inc. (Shanghai, China). Phosphoric acid (H3PO4, 85%) and cupric acetate (Cu(CH3OO)2·H2O, 98%) were obtained from Sinopharm Chemical Reagent Co. Ltd. (Shanghai, China). Ionic liquids 1-butyl-3-methyl imidazolium bromide ([BMIM]Br, 99%) was purchased from Lanzhou Zhong Kekaite Co. Ltd. (Lanzhou, China).

2.2. Catalyst synthesis

The synthesis experiment was carried out in a 100 mL round-bottom flask charged with [BMIM]Br as solvent. After adding the H3PO4, the round-bottom flask was heated to 80 °C under mechanical stirring (400 rpm). Then, TEAOH, Al[OCH(CH3)2]3, Cu(CH3OO)2·H2O, and HF were added in order under mechanical stirring to form a solution with a molar ratio of 20 [BMIM]Br[thin space (1/6-em)]:[thin space (1/6-em)]2.55 P2O5[thin space (1/6-em)]:[thin space (1/6-em)]1.5 TEAOH[thin space (1/6-em)]:[thin space (1/6-em)]1.0 Al2O3[thin space (1/6-em)]:[thin space (1/6-em)]xCuO[thin space (1/6-em)]:[thin space (1/6-em)]0.6 HF (where x = 0.006, 0.012, 0.018, 0.024). Subsequently, the solution was rapidly heated to 140 °C and then maintained at 140 °C for 1 h under mechanical stirring (70 rpm). After cooled down to room temperature, the product was filtered and washed with deionized water for several times. The solid product was dried at 120 °C overnight followed by calcined at 550 °C for 10 h to obtain CuAPO-5 sample.

2.3. Catalyst characterization

X-ray diffraction (XRD) was conducted on Bruker D8 Advance with Cu Kα radiation source at λ = 1.54056 nm. The N2 adsorption–desorption isotherms at 77 K were performed on a Quantachrome Autosorb-iQ-C instrument. Morphology of the synthesized CuAPO-5 samples was examined by a Verios G4 UC scanning electron microscope (SEM). The compositions of the sample were determined by the X-ray fluorescence technique (XRF). The XRF analysis was performed on a Rigaku ZSX Primus II XRF spectrometer. NH3 temperature-programmed desorption (NH3-TPD) of the catalyst was carried out on a Tianjin XQ TP-5076 instrument equipped with a mass spectrum detector. The sample (200 mg) was evacuated at 500 °C for 1 h in the flow of Ar and then cooled down to 100 °C. The adsorption of NH3 was performed with the flow of 5% (v/v) NH3/Ar at 100 °C. The NH3 desorption was carried out from 100 °C to 600 °C with a heating rate of 10 °C min−1. EPR spectra were recorded on a Bruker Elexsys E500 spectrometer.

2.4. Catalytic activity test

The catalytic performance in fructose dehydration to 5-hydroxymethylfurfural was determined in a 100 mL three-neck flask. In each experiment, 40 g of [BMIM]Br was loaded in flask under mechanical stirring (400 rpm) and then the flask was heated in the oil bath at 110 °C for 60 min. Subsequently, 0.40 g of catalyst was added into the reactor and then stirred at 110 °C for 5 min. The reaction time started to count as soon as the 4.0 g of fructose was put into the solution. The reaction mixture was collected from reactor using pipette. The obtained sample was filtered and diluted for further product analysis.

For catalyst recycling tests, the 0.06-CuAPO-5 catalyst was separated from the reaction mixture by filtration and washed with deionized water for several times. Subsequently, the recycled catalyst was dried in an oven at 120 °C for 2 h and then calcined in a muffle furnace at 550 °C for 3 h before using in the next reaction.

The quantitative analysis of fructose was performed by HPLC using an Bio-Rad aminex column HPX-87H column and RID detector. H2SO4 (5 mmol L−1) was used as the mobile phase at a flow rate of 0.4 mL min−1, and the column temperature was set at 30 °C. Quantitative analysis of HMF was performed using Agilent 1260 HPLC Infinity instrument equipped with a UV detector and Agilent ZORBAX Extend-C18 column. A mixture of water and methanol (95[thin space (1/6-em)]:[thin space (1/6-em)]5 (v/v)) was used as the mobile phase at a flow rate of 1.0 mL min−1, and the column temperature was maintained at 30 °C.

3. Results and discussion

3.1. Catalyst characterization

A series of CuAPO-5 molecular sieves with different Cu contents were ionothermally prepared. The X-ray diffraction (XRD) patterns of the CuAPO-5 samples exhibited similar characteristics of the AFI structure (Fig. 2a).28 The absence of any individual Cu-related phase indicates that the Cu component might be integrated into the lattice of the AFI structure or its content was too low to be detected even if agglomerated.25 The type-IV hysteresis loop can be seen in N2 adsorption–desorption isotherms (Fig. 2b), demonstrating the presence of mesopores.29 This was further confirmed by the pore size distribution in Fig. 2b.
image file: c9ra07217a-f2.tif
Fig. 2 XRD patterns (a), N2 adsorption–desorption isotherms and pore size distribution inserted (b) of the CuAPO-5 samples.

Table 1 summarizes the chemical compositions and textural properties of all CuAPO-5 samples. Although the actual Cu content in the catalysts gradually raised with the increasing feed amount of Cu in the gel, only trace Cu could be kept in the catalysts. This result is quite different from the hydrothermally synthesized CuAPO-5 catalysts with much higher Cu content,24 which could be related to the fact that the presence of the amine would go against the incorporation of heteroatoms element in our case.22 Nevertheless, these tiny amounts of Cu significantly altered the physicochemical property of CuAPO-5 samples. The BET surface area increased from 197.0 to 217.4 m2 g−1 and then declined to 162.9 m2 g−1 with the increasing Cu content. Fig. 3 depicts the morphologies of all CuAPO-5 samples that were agglomerated rod-like crystals, which is always observed on the ionothermally synthesized MAPO-5 molecular sieves.30 Many cavities could be created within the aggregates to form mesoscale porosity during the ionothermal synthesis.31 As the Cu content increased, the agglomerated species became more abundant and bigger, which would cause possible pore blocking and induce inferior BET surface area.

Table 1 Chemical compositions and physicochemical properties of the CuAPO-5 samples
Sample Content of Cu SBETb (m2 g−1) Vmicroc (cm3 g−1) Vmesod (cm3 g−1) Number of acid sitese (mmol of NH3 per g)
Gel Samplea Weak (<200 °C) Strong (200–300 °C) Total acid
a Determined by XRF.b Calculated by BET method.c Estimated by t-plot method.d Calculated by a subtraction of total pore volume at a relative pressure of P/P0 = 0.99 from the micropore pore volume obtained from the t-plot.e Determined by NH3 desorption (chemisorbed at 100 °C).
0.03-CuAPO-5 1.5% 23 ppm 197.0 0.06 0.13 0.08 0.12 0.20
0.06-CuAPO-5 3.0% 34 ppm 217.4 0.07 0.14 0.10 0.12 0.22
0.09-CuAPO-5 4.5% 52 ppm 193.1 0.06 0.13 0.11 0.12 0.23
0.12-CuAPO-5 6.0% 70 ppm 162.9 0.05 0.12 0.12 0.13 0.25



image file: c9ra07217a-f3.tif
Fig. 3 SEM images of the CuAPO-5 samples ((a): 0.03-CuAPO-5; (b): 0.06-CuAPO-5; (c): 0.09-CuAPO-5; (d): 0.12-CuAPO-5).

NH3-TPD is an effective tool to verify the incorporation of heteroatoms into the AlPO framework.33 As seen in Fig. 4a, all samples exhibited two desorption peaks, which could be ascribed to the ammonia adsorbing onto the weak and relatively stronger acid sites, respectively. With the increase in the copper content, both the total amount of acid sites and acid strength gradually increased (Table 1). The strong acid sites should be attributed to the substitution of heteroatoms for Al3+ in the framework.32 In addition, the signals of G = 2.054 assigned to the isolated Cu2+ species locating in the framework as tetrahedrally coordinated Cu could be observed in the EPR spectrum of the samples (Fig. 4b).25 Furthermore, its intensity enhanced with the increasing Cu content, suggesting more copper atoms located in the framework. Based on the above results, it is reasonable to conclude that copper was successfully incorporated into the AFI framework.


image file: c9ra07217a-f4.tif
Fig. 4 NH3-TPD profiles (a) and EPR spectrum (b) of the CuAPO-5 samples.

3.2. Catalytic performance

The catalytic performance of CuAPO-5 catalysts in fructose dehydration to HMF was evaluated in [BMIM]Br at 110 °C (Fig. 5). In the blank test without catalyst, the conversion of fructose was lower than 10% during the first 30 min and approached to 31.7% after the reaction for 60 min, yielding less than 7% HMF. This result suggested that the [BMIM]Br could catalyze the dehydration reaction,33 but its activity was rather low under the present reaction conditions. With the presence of CuAPO-5 catalysts, both fructose conversion and HMF yield sharply increased. For 0.03-CuAPO-5, 98.3% conversion and 88.7% yield were achieved after 30 min of reaction. The fructose conversion and HMF yield finally reached 99.1% and 92.0%, respectively. 0.06-CuAPO-5 as the most active sample gave an almost complete conversion of fructose and 90.6% yield of HMF within 8 min. After the reaction for 15 min, the HMF yield increased to 93.8%. However, for 0.09-CuAPO-5 and 0.12-CuAPO-5 samples with higher Cu content, both reaction activity and HMF yield declined to some extent. It should be noted that the HMF yield on these CuAPO-5 catalysts was higher than most of the reported zeolitic catalysts (Table 2), suggesting that the ionothermally prepared CuAPO-5 was also a good candidate for the efficient production of HMF.
image file: c9ra07217a-f5.tif
Fig. 5 The catalytic performances of the samples in dehydration of fructose to HMF. Reaction conditions: 40 g [BMIM]Br, 4.0 g fructose, 0.4 g catalyst, 110 °C.
Table 2 Catalytic performances of the different zeolitic catalysts in dehydration of fructose to HMF
Catalyst Solvent HMF yield (%) Reference
MeSAPO-5 Aqueous/organic phase 73.9 14
MeSAPO-11 H2O, DMSO, MIBK and SBA 78.2 15
H-mordenite H2O/MIBK 74.0 10
ZSM-5 H2O/MIBK 75.1 36
MCM-22 H2O/MIBK 70.3 36
KIT-6 DMSO 84.1 9
KL [BMIM]Br 99.1 11
HY Water/GBL 69.2 37
0.06-CuAPO-5 [BMIM]Br 93.8 This work
0.12-CuAPO-5 [BMIM]Br 85.5 This work


Compared with 0.03-CuAPO-5, 0.06-CuAPO-5 exhibited higher surface area, pore volume, and stronger acidity, which were believed to be the positive factors for dehydrating fructose. Thus, the improved performance on the 0.06-CuAPO-5 sample is reasonable. Further increase in the Cu content raised the acidity but dropped the BET surface area and pore volume, resulting in the inferior performance of 0.09-CuAPO-5 and 0.12-CuAPO-5. Therefore, for the acid-catalyzed reaction like fructose dehydration, the acidity was not the only determining factor and the effect of porosity on mass transfer efficiency should be highlighted.34 According to the literature, the diffusion limitation in pore channels of molecular sieves would greatly restrict the conversion of furanic compounds.35 Catalyst reusability is also a required property and we tested the catalytic performance of the recovered 0.06-CuAPO-5 sample under the same reaction conditions. As shown in Fig. 6, the sample maintained its high activity even after five recycles, indicating a promising future of CuAPO-5 catalysts. In addition, the chemical compositions and physicochemical properties of the 0.06-CuAPO-5 catalyst recovered after the fifth cycle were also characterized. The Cu content increased to 40 ppm, which might be due to the losing of a small amount of Al or P in the regeneration process. Moreover, the BET surface area (207.2 m2 g−1) and acid amount (0.21 mmol g−1) decreased only slightly compared with the corresponding values of the fresh 0.06-CuAPO-5 sample, which well explained the superior recyclability and reusability of CuAPO-5 catalysts.


image file: c9ra07217a-f6.tif
Fig. 6 The reusability of 0.06-CuAPO-5 sample in dehydration of fructose to HMF. Reaction conditions: 40 g [BMIM]Br, 4.0 g fructose, 0.4 g catalyst, 110 °C (3 min for cycle usage test).

4. Conclusions

In this work, the trace Cu substituted aluminophosphate molecular sieves were successfully synthesized via an ionothermal method. The characterization results indicated that the Cu substitution could significantly change the physicochemical properties of the catalysts. The 0.06-CuAPO-5 sample displayed the best performance for fructose dehydration to HMF in [BMIM]Br ionic liquid and obtained a high yield of HMF (93.8%), which could be explained by its suitable acidity and better mass transfer efficiency.

Conflicts of interest

The authors declare no conflict of interest.

Acknowledgements

This work was financially supported by the Key Research Program of Frontier Sciences of CAS (No. QYZDB-SSW-JSC037), Key Research Program of Chinese Academy of Sciences (ZDRW-CN-2016-1), Zhejiang Provincial Natural Science Foundation of China (LR16B030001, LQ19B060002, and LY19B030003), K. C. Wong Education Foundation (rczx0800), Fujian Institute of Innovation of Chinese Academy of Sciences (FJCXY18020202).

References

  1. Z. R. Zhang, J. L. Song and B. X. Han, Chem. Rev., 2017, 117, 6834–6880 CrossRef CAS.
  2. J. J. Bozell and G. R. Petersen, Green Chem., 2010, 12, 539–554 RSC.
  3. M. Balakrishnan, E. R. Sacia and A. T. Bell, Green Chem., 2012, 14, 1626–1634 RSC.
  4. X. Y. Wan, C. M. Zhou, J. S. Chen, W. P. Deng, Q. H. Zhang, Y. H. Yang and Y. Wang, ACS Catal., 2014, 4, 2175–2185 CrossRef CAS.
  5. H. B. Zhao, J. E. Holladay, H. Brown and Z. C. Zhang, Science, 2007, 316, 1597–1600 CrossRef CAS.
  6. B. Agarwal, K. Kailasam, R. S. Sangwan and S. Elumalai, Renewable Sustainable Energy Rev., 2018, 82, 2408–2425 CrossRef CAS.
  7. R. A. Sheldon and R. S. Downing, Appl. Catal., A, 1999, 189, 163–183 CrossRef CAS.
  8. Y. Li, H. Liu, C. H. Song, X. M. Gu, H. M. Li, W. S. Zhu and S. Yin, Bioresour. Technol., 2013, 133, 347–353 CrossRef CAS.
  9. H. Hafizi, A. N. Chermahini, M. Saraji and G. Mohammadnezhad, Chem. Eng. J., 2016, 294, 380–388 CrossRef CAS.
  10. C. Moreau, R. Durand, S. Razigade, J. Duhamet, P. Faugeras, P. Rivalier, P. Ros and G. Avignon, Appl. Catal., A, 1996, 145, 211–224 CrossRef CAS.
  11. Z. S. Ma, H. L. Hu, Z. Q. Sun, W. T. Fang, J. Zhang, L. F. Yang, Y. J. Zhang and L. Wang, ChemSusChem, 2017, 10, 1669–1674 CrossRef CAS.
  12. M. Hartmann and L. Kevan, Chem. Rev., 1999, 99, 635–663 CrossRef CAS.
  13. J. H. Yu and R. R. Xu, Chem. Soc. Rev., 2006, 35, 593–604 RSC.
  14. H. Shao, J. J. Chen, J. Zhong, Y. X. Leng and J. Wang, Ind. Eng. Chem. Res., 2015, 54, 1470–1477 CrossRef CAS.
  15. J. J. Zheng, J. J. Chen, H. Shao, J. Wang and X. N. Sun, J. Renewable Sustainable Energy, 2017, 9, 063103 CrossRef.
  16. L. X. Zhang, G. Y. Xi, Z. Chen, Z. Y. Qi and X. C. Wang, Chem. Eng. J., 2017, 307, 877–883 CrossRef CAS.
  17. E. R. Cooper, C. D. Andrews, P. S. Wheatley, P. B. Webb, P. Wormald and R. E. Morris, Nature, 2004, 430, 1012–1016 CrossRef CAS.
  18. L. Wang, Y. P. Xu, Y. Wei, J. C. Duan, A. B. Chen, B. C. Wang, H. J. Ma, Z. J. Tian and L. W. Lin, J. Am. Chem. Soc., 2006, 128, 7432–7433 CrossRef CAS PubMed.
  19. P. Wasserscheid and W. Keim, Angew. Chem., Int. Ed., 2000, 39, 3772–3789 CrossRef CAS.
  20. E. R. Parnham and R. E. Morris, Chem. Mater., 2006, 18, 4882–4887 CrossRef CAS.
  21. M. Sánchez-Sánchez, Á. A. Romero, I. Pinilla-Herrero and E. Sastre, Catal. Today, 2017, 296, 239–246 CrossRef.
  22. L. Wang, Y. P. Xu, B. C. Wang, S. J. Wang, J. Y. Yu, Z. J. Tian and L. W. Lin, Chem.–Eur. J., 2008, 14, 10551–10555 CrossRef CAS PubMed.
  23. Y. P. Xu, Z. J. Tian, Z. S. Xu, B. C. Wang, P. Li, S. J. Wang, Y. Hu, Y. C. Ma, K. L. Li, Y. J. Liu, J. Y. Yu and L. W. Lin, Chin. J. Catal., 2005, 26, 446–448 CAS.
  24. X. H Zhao, X. X. Zhao, Z. X. Hao, X. P. Gao and L. Zhong, J. Porous Mater., 2018, 25, 1007–1016 CrossRef.
  25. Q. P. Ke, M. Z. Wu, H. Z. Yu and G. Z. Lu, ChemCatChem, 2017, 9, 733–737 CrossRef CAS.
  26. D. G. Nicholson and M. H. Nilsen, J. Mater. Chem., 2000, 10, 1965–1971 RSC.
  27. S. K. Saha, S. B. Waghmode, H. Maekawa, K. Komura, Y. Kubota, Y. Sugi, Y. Oumi and T. Sano, Microporous Mesoporous Mater., 2005, 81, 289–303 CrossRef CAS.
  28. S. C. Xu, Z. C. Zhao, M. Y. Hu, X. W. Han, J. Z. Hu and X. H. Bao, Microporous Mesoporous Mater., 2016, 223, 241–246 CrossRef CAS.
  29. H. L. Hu, J. H. Lyu, J. Y. Rui, J. Cen, Q. F. Zhang, Q. T. Wang, W. W. Han and X. N. Li, Catal. Sci. Technol., 2016, 6, 2647–2652 RSC.
  30. Y. P. Xu, Z. J. Tian, S. J. Wang, Y. Hu, L. Wang, B. C. Wang, Y. C. Ma, L. Hou, J. Y. Yu and L. W. Lin, Angew. Chem., Int. Ed., 2006, 45, 3965–3970 CrossRef CAS.
  31. K. Zhu, J. M. Sun, J. Liu, L. Q. Wang, H. Y. Wan, J. Z. Hu, Y. Wang, C. H. F. Peden and Z. M. Nie, ACS Catal., 2011, 1, 682–690 CrossRef CAS.
  32. M. da S. Machado, J. Pérez-Pariente, E. Sastre, D. Cardoso, M. V. Giotto, J. L. García-Fierro and V. Fornész, J. Catal., 2002, 205, 299–308 CrossRef CAS.
  33. Y. N. Li, J. Q. Wang, L. N. He, Z. Z. Yang, A. H. Liu, B. Yu and C. R. Luan, Green Chem., 2012, 14, 2752–2758 RSC.
  34. M. Ruby and F. Schüth, Green Chem., 2016, 18, 3422–3429 RSC.
  35. S. Alipour, H. Omidvarborna and D. Kim, Renewable Sustainable Energy Rev., 2017, 71, 908–926 CrossRef CAS.
  36. T. Y. Cheng, P. Y. Chao, Y. H. Huang, C. C. Li, H. Y. Hsu, Y. S. Chao and T. C. Tsai, Microporous Mesoporous Mater., 2016, 233, 148–153 CrossRef CAS.
  37. L. Q. Wang, H. Q. Guo, Q. L. Xie, J. G. Wang, B. Hou, L. T. Jia, J. L. Cui and D. B. Li, Appl. Catal., A, 2019, 572, 51–60 CrossRef CAS.

Footnote

The first two authors contributed equally to this work.

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