Hydrothermal synthesis of alkali-free chabazite zeolites
Source abstract
Abstract
Alkali-free siliceous CHA zeolites with a wide Si/Al ratio ranging from 11 to infinity have been synthesized in hydroxide and fluoride media using either N,N,N-Trimethyl-1-adamantammonium (TMAda), N,N,N-Dimethylethylcyclohexyl ammonium (DMECHA) cations, or a mixture thereof. TMAda, in combination with other low-cost organic templates, allowed the formation of pure silica CHA without any impurities in the synthesis gel with an H2O/SiO2 ratio of 3. Single-phase crystalline pure silica CHA was produced by DMECHA within a very narrow range of H2O/SiO2 ratio, and small deviations in the water content from this range led to the formation of a slightly less dense zeolite beta phase. Alkali-free siliceous CHA zeolites possessing a high crystallinity and a variety of particle sizes were successfully prepared for the first time using a low-cost DMECHA template, particularly by a direct interzeolite transformation of FAU zeolites having the same secondary building unit of double-6-rings (D6Rs). This makes DMECHA an attractive organic structure-directing agent (OSDA) for wide applications of CHA zeolites as catalysts and adsorbents.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Zeolite Catalysis and Synthesis · Mesoporous Materials and Catalysis · Covalent Organic Framework Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (50)
Show source-provided references
1. P. Tian, Y. Wei, M. Ye, Z. Liu, ACS Catal. 5(3), 1922–1938 (2015)10.1021/acscatal.5b00007 ↗
2. D. Chen, K. Moljord, A. Holmen, Microporous Mesoporous Mater. 164, 239–250 (2012)10.1016/j.micromeso.2012.06.046 ↗
3. Y. Bhawe, M. Moliner-Marin, J.D. Lunn, Y. Liu, A. Malek, M. Davis, ACS Catal. 2(12), 2490–2495 (2012)10.1021/cs300558x ↗
4. X. Li, J. Jiang, PCCP 20(21), 14322–14330 (2018)10.1039/C8CP00572A ↗
5. M.R. Gogate, Pet. Sci. Technol. 37(5), 559–565 (2019)10.1080/10916466.2018.1555589 ↗
6. F. Gao, J. Kwak, J. Szanyi, C.F. Peden, Top. Catal. 56(15–17), 1441–1459 (2013)10.1007/s11244-013-0145-8 ↗
7. S. Brandenberger, O. Kröcher, A. Tissler, R. Althoff, Catal. Rev. 50(4), 492–531 (2008)10.1080/01614940802480122 ↗
8. A.M. Beale, F. Gao, I. Lezcano-Gonzalez, C.H.F. Peden, J. Szanyi, Chem. Soc. Rev. 44(20), 7371–7405 (2015)10.1039/C5CS00108K ↗
9. C. Paolucci, J.R. Di Iorio, F.H. Ribeiro, R. Gounder, W.F. Schneider, Adv. Catal. 59, 1–107 (2016)10.1016/bs.acat.2016.10.002 ↗
10. B. Guan, R. Zhan, H. Lin, Z. Huang, Appl. Therm. Eng. 66(1), 395–414 (2014)10.1016/j.applthermaleng.2014.02.021 ↗
11. F. Gao, J. Szanyi, Appl. Catal. A 560, 185–194 (2018)10.1016/j.apcata.2018.04.040 ↗
12. T. Ryu, Y. Kang, I.-S. Nam, S.B. Hong, React. Chem. Eng. 4(6), 1050–1058 (2019)10.1039/C9RE00007K ↗
13. HY Chen, Cu/Zeolite scr catalysts for automotive diesel nox emission control. In Urea-SCR Technology for deNOx After Treatment of Diesel Exhausts, eds I Nova, E Tronconi, Springer: New York, 2014, pp 123–14710.1007/978-1-4899-8071-7_5 ↗
14. F. Gao, J.H. Kwak, J. Szanyi, C.H.F. Peden, Top. Catal. 56(15), 1441–1459 (2013)10.1007/s11244-013-0145-8 ↗
15. Y. Shan, X. Shi, G. He, K. Liu, Z. Yan, Y. Yu, H. He, J. Phy Chem C 122(45), 25948–25953 (2018)10.1021/acs.jpcc.8b05930 ↗
16. M.J. Wulfers, S. Teketel, B. Ipek, R.F. Lobo, Chem. Commun. 51(21), 4447–4450 (2015)10.1039/C4CC09645B ↗
17. E.A. Eilertsen, S. Bordiga, C. Lamberti, A. Damin, F. Bonino, B. Arstad, S. Svelle, U. Olsbye, K.P. Lillerud, ChemCatChem 3(12), 1869–1871 (2011)10.1002/cctc.201100281 ↗
18. D.H. Olson, M.A. Camblor, L.A. Villaescusa, G.H. Kuehl, Microporous Mesoporous Mater. 67(1), 27–33 (2004)10.1016/j.micromeso.2003.09.025 ↗
19. T.D. Pham, M.R. Hudson, C.M. Brown, R.F. Lobo, Chemsuschem 7(11), 3031–3038 (2014)10.1002/cssc.201402555 ↗
20. T.D. Pham, Q. Liu, R.F. Lobo, Langmuir 29(2), 832–839 (2013)10.1021/la304138z ↗
21. T. Du, X. Fang, L. Liu, J. Shang, B. Zhang, Y. Wei, H. Gong, S. Rahman, E.F. May, P.A. Webley, G. Li, Chem. Commun. 54(25), 3134–3137 (2018)10.1039/C8CC00634B ↗
22. M. Lee, S. Hong, D. Kim, E. Kim, K. Lim, J.C. Jung, H. Richter, J.-H. Moon, N. Choi, J. Nam, J. Choi, ACS Appl. Mater. Interfaces 11(4), 3946–3960 (2019)10.1021/acsami.8b18854 ↗
23. J. Smith, Acta Crystallogr. 15(9), 835–845 (1962)10.1107/S0365110X62002236 ↗
24. R.M. Barrer, Zeolites 1(3), 130–140 (1981)10.1016/S0144-2449(81)80001-2 ↗
25. G.A. Nasser, O. Muraza, T. Nishitoba, Z. Malaibari, T.K. Al-Shammari, T. Yokoi, Microporous Mesoporous Mater. 274, 277–285 (2019)10.1016/j.micromeso.2018.07.020 ↗
26. S. Miyagawa, K. Miyake, Y. Hirota, N. Nishiyama, M. Miyamoto, Y. Oumi, S. Tanaka, Microporous Mesoporous Mater. 278, 219–224 (2019)10.1016/j.micromeso.2018.11.037 ↗
27. SI Zones, Zeolite SSZ-13 and its method of preparation. Google Patents, 1985
28. MJ.Diaz-Cabanas, A. Barrett, P. Chem. Commun. 1998, (17), 1881–188210.1039/a804800b ↗
29. SJ Miller, LT Yuen, Preparation of zeolites using novel structure directing agents. Google Patents, 200910.1016/S1351-4180(09)70487-8 ↗
30. M. Itakura, T. Inoue, A. Takahashi, T. Fujitani, Y. Oumi, T. Sano, Chem. Lett. 37(9), 908–909 (2008)10.1246/cl.2008.908 ↗
31. TM Davis, SA Elomari, SI Zones, Method for preparing cha-type molecular sieves using colloidal aluminosilicate. Google Patents, 2014.
32. B. Chen, R. Xu, R. Zhang, N. Liu, Environ. Sci. Technol. 48(23), 13909–13916 (2014)10.1021/es503707c ↗
33. R. Xu, R. Zhang, N. Liu, B. Chen, S. Zhang Qiao, ChemCatChem 7(23), 3842–3847 (2015)10.1002/cctc.201500771 ↗
34. L. Ren, L. Zhu, C. Yang, Y. Chen, Q. Sun, H. Zhang, C. Li, F. Nawaz, X. Meng, F.-S. Xiao, Chem. Commun. 47(35), 9789–9791 (2011)10.1039/c1cc12469b ↗
35. N. Martin, M. Moliner, A. Corma, Chem. Commun. 51(49), 9965–9968 (2015)10.1039/C5CC02670A ↗
36. BN Bhadra, PW Seo, NA Khan, JW Jun, TW Kim, C.-U Kim, SH Jhung, Catal. Today 2017
37. G Cao, JF Brody, MJ Shah, Light olefin selective oxygenate conversion process using CHA framework type aluminosilicate. Google Patents, 2010
38. MM Mertens, SN Vaughn, G Cao, LRM Martens, M Afeworki, Synthesis of chabazite-containing molecular sieves and their use in the conversion of oxygenates to olefins. Google Patents, 2012
39. X. Wang, Q. Wu, C. Chen, S. Pan, W. Zhang, X. Meng, S. Maurer, M. Feyen, U. Muller, F.-S. Xiao, Chem. Commun. 51(95), 16920–16923 (2015)10.1039/C5CC05980A ↗
40. T.D. Pham, R. Xiong, S.I. Sandler, R.F. Lobo, Microporous Mesoporous Mater. 185, 157–166 (2014)10.1016/j.micromeso.2013.10.030 ↗
41. J.R. Di Iorio, R. Gounder, Chem. Mater. 28(7), 2236–2247 (2016)10.1021/acs.chemmater.6b00181 ↗
42. E.A. Eilertsen, B. Arstad, S. Svelle, K.P. Lillerud, Microporous Mesoporous Mater. 153, 94–99 (2012)10.1016/j.micromeso.2011.12.026 ↗
43. L.A. Villaescusa, I. Bull, P.S. Wheatley, P. Lightfoot, R.E. Morris, J. Mater. Chem. 13(8), 1978–1982 (2003)10.1039/B300728F ↗
44. H. Al Jabri, K. Miyake, K. Ono, M. Nakai, Y. Hirota, Y. Uchida, M. Miyamoto, N. Nishiyama, Microporous Mesoporous Mater. 278, 322–326 (2019)10.1016/j.micromeso.2019.01.006 ↗
45. A.W. Burton, G.S. Lee, S.I. Zones, Microporous Mesoporous Mater. 90(1–3), 129–144 (2006)10.1016/j.micromeso.2005.11.022 ↗
46. AW Burton, SI Zones, Chapter 5 Organic molecules in zeolite synthesis: Their preparation and structure-directing effects. In Stud. Surf. Sci. Catal., Eds. HVBAC Jiří Čejka, S Ferdi, Elsevier, 2007, 168, pp 137–17910.1016/S0167-2991(07)80793-2 ↗
47. M.A. Camblor, L.A. Villaescusa, M.J. Díaz-Cabañas, Top. Catal. 9(1–2), 59–76 (1999)10.1023/A:1019154304344 ↗
48. J. Dědeček, S. Sklenak, C. Li, F. Gao, J. Brus, Q. Zhu, T. Tatsumi, J. Phys. Chem. C 113(32), 14454–14466 (2009)10.1021/jp9042232 ↗
49. Q. Zhu, J.N. Kondo, R. Ohnuma, Y. Kubota, M. Yamaguchi, T. Tatsumi, Microporous Mesoporous Mater. 112(1–3), 153–161 (2008)10.1016/j.micromeso.2007.09.026 ↗
50. A.V. Goretsky, L.W. Beck, S.I. Zones, M.E. Davis, Microporous Mesoporous Mater. 28(3), 387–393 (1999)10.1016/S1387-1811(98)00307-2 ↗