Abstract

Zinc hydroxide chloride particles of ZHC (simonkolleite, Zn 5(OH) 8Cl 2·H 2O) and layered double hydroxides (LDH, Zn–Al–Cl) were prepared by hydrolysis of ZnCl 2 solutions dissolving AlCl 3 at Al/Zn = 0.1 and 0.6 in atomic ratio, respectively. The anion-exchange and thermal change of ZHC and LDH were investigated by XRD, TEM, FTIR, analysis of Zn, Al, and Cl and gas adsorption of N 2, H 2O, and CCl 4. The formed ZHC and LDH particles were hexagonal thin plates and irregularly shaped thin plates, respectively. LDH was more easily ion-exchanged with CO 3 2− and SO 4 2− compared to ZHC. The layered structure of LDH was damaged by the ion-exchange with SO 4 2− but not CO 3 2−, whereas that of ZHC was kept after the ion-exchange with both the anions. The TEM observation of the ZHC and LDH particles outgassed at different temperatures of 75–400 °C revealed that exfoliation takes place on outgassing ZHC at 100–150 °C but not occurs in LDH. ZHC showed a high H 2O adsorption selectivity when outgassed below 100 °C, however the adsorption selectivity completely disappeared above 125 °C where the exfoliation took place. On the other hand, LDH exhibited less adsorption selectivity than ZHC though the selectivity was held after outgassed at 400 °C. The facilitated delamination of ZHC indicates that ZHC exhibits weaker interlalyer attractive force than LDH in vacuo.

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