Cellulose-type binder enabling CuCl2 supported on nanoporous bayerite to have high CO adsorption ability via reduction of Cu2+ to Cu
Previously, we developed a powder-form nanoporous CO-selective adsorbent synthesized via thermal monolayer dispersion of CuCl on bayerite, showing high CO adsorption capacity (48.5 cm 3 g −1 ) and a high CO/CO 2 selectivity (12.4). For its industrial applications, it is necessary to pelletize it, av...
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Veröffentlicht in: | The Korean journal of chemical engineering 2022, 39(3), 264, pp.684-694 |
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Sprache: | eng |
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Zusammenfassung: | Previously, we developed a powder-form nanoporous CO-selective adsorbent synthesized via thermal monolayer dispersion of CuCl on bayerite, showing high CO adsorption capacity (48.5 cm
3
g
−1
) and a high CO/CO
2
selectivity (12.4). For its industrial applications, it is necessary to pelletize it, avoiding pressure-drop problems. Here, we demonstrate a facile three-step method of pelletizing a CuCl/bayerite: 1) physical mixing of CuCl, methyl-cellulose, inorganic-binder, and bayerite, 2) pelletizing, and 3) thermal treatment at 573 K under vacuum. The pelletized adsorbent shows high CO adsorption capacity (42 cm
3
g
−1
), CO/CO
2
selectivity (12), and commercial-level mechanical strength (1.3 kg
f
). Notably, the added methyl-cellulose binder has reducing role that maintains the initial CO adsorption capacity for 100 days’ exposure to humid air-condition, although CuCl-based adsorbent easily lost CO adsorption ability owing to oxidation of Cu
+
to Cu
2+
. CuCl
2
, showing no specific interaction with CO, was converted to Cu
+
by the methyl-cellulose. Thus, adsorbent prepared using CuCl
2
instead of CuCl with the methyl-cellulose also showed high CO adsorption capacity (31.6 cm
3
g
−1
) and maintained the initial capacity after seven days’ exposure. The reducing role of the methyl-cellulose binder allows inexpensive and feasible synthesis of the CO-adsorbent using CuCl
2
that can be easily dispersed on bayerite, without additional reduction treatment. |
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ISSN: | 0256-1115 1975-7220 |
DOI: | 10.1007/s11814-021-0928-8 |