In situ Raman spectroscopy analysis of local structure in dry gel for zeolite beta synthesis
Source abstract
Abstract
Abstract To investigate faster crystallization of zeolite beta by the dry‐gel conversion method, the local structure of the dry gel before synthesis was quantitatively evaluated using in situ Raman spectroscopy during the drying process. The dry gel prepared from Si and Al sources, and tetraethylammonium hydroxide solution was crystallized after several hours by the dry‐gel conversion method. The conformational change of TEA + cations was observed during the drying process by the deconvolution of the spectrum, and the conformational change was larger than that during the synthesis process. The rate of conformational change was increased with the drying temperature, and the apparent activation energy was estimated to be 68.2 kJ/mol. The generation and transformation of double three‐membered silicate rings (D3Rs) and 4‐2 type secondary building units (SBUs), which are essential for the crystallization of zeolite beta, were observed during the drying process. The transformation from D3R to 4‐2 SBU in the dry gel during drying process could be confirmed quantitatively by the difference of the time variation for the amounts of these silicate building units estimated by in situ observation.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Zeolite Catalysis and Synthesis · Mesoporous Materials and Catalysis · Glass properties and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Life Science and Applied Chemistry Graduate School of Engineering, Nagoya Institute of Technology Nagoya Aichi Japan
Funding
Japan Science and Technology Agency
References (29)
Show source-provided references
1. 10.1021/jacs.5b1104610.1021/jacs.5b11046 ↗
2. 10.1016/0144-2449(94)90099-X10.1016/0144-2449(94)90099-X ↗
3. 10.1021/ie030035i10.1021/ie030035i ↗
4. 10.3131/jvsj.49.20510.3131/jvsj.49.205 ↗
5. 10.1016/j.micromeso.2008.04.00110.1016/j.micromeso.2008.04.001 ↗
6. 10.1021/cm302099510.1021/cm3020995 ↗
7. 10.1002/chem.20160051110.1002/chem.201600511 ↗
8. 10.1016/0144-2449(92)90071-V10.1016/0144-2449(92)90071-V ↗
9. 10.1002/adma.1996008091310.1002/adma.19960080913 ↗
10. 10.1023/A:101910642118310.1023/A:1019106421183 ↗
11. 10.1016/S1387-1811(02)00412-210.1016/S1387-1811(02)00412-2 ↗
12. 10.1021/jp066804410.1021/jp0668044 ↗
13. 10.1016/j.micromeso.2013.08.02610.1016/j.micromeso.2013.08.026 ↗
14. 10.1016/j.matchemphys.2013.05.05310.1016/j.matchemphys.2013.05.053 ↗
15. 10.1002/anie.20160905310.1002/anie.201609053 ↗
16. 10.1111/jace.1753910.1111/jace.17539 ↗
17. 10.1039/a909867d10.1039/a909867d ↗
18. 10.1002/asia.20100023410.1002/asia.201000234 ↗
19. 10.1021/jp109897510.1021/jp1098975 ↗
20. 10.1021/cm801167e10.1021/cm801167e ↗
21. 10.1021/cm900462u10.1021/cm900462u ↗
22. 10.1039/c3ce40784e10.1039/c3ce40784e ↗
23. 10.1021/ja302233510.1021/ja3022335 ↗
24. 10.1016/j.micromeso.2013.08.00810.1016/j.micromeso.2013.08.008 ↗
25. 10.1002/1097-4555(200011)31:11<979::AID-JRS629>3.0.CO;2-Y10.1002/1097-4555(200011)31:11<979::AID-JRS629>3.0.CO;2-Y ↗
26. 10.1021/jp062911m10.1021/jp062911m ↗
27. 10.1007/BF0020297510.1007/BF00202975 ↗
28. Three‐dimensional network structure of quenched melts (glass) in the systems SiO2‐NaAlO2, SiO2‐CaAl2O4 and SiO2‐MgAl2O4
29. 10.1021/la00038a06810.1021/la00038a068 ↗