Layered doubled hydroxides (LDHs) are known to be an interesting class of 2D layered materials, with a wide range of possible composition and a flexible structure suitable for topochemical reactions. Thus, LDHs have been applying in different fields, such as catalysis, energy storage and all the applications in which a high exchange capability (of both cations and anions) is required. For remediation purpose, a MgFe-Cl LDH $${[({\mathrm{Mg}}_{0.66}^{2+}{\mathrm{Fe}}_{0.33}^{3+}{\left(\mathrm{OH}\right)}_{2}]}^{0.33+}{({\mathrm{Cl}}_{0.33}^{-})}^{0.33-}$$
[
(
Mg
0.66
2
+
Fe
0.33
3
+
OH
2
]
0.33
+
(
Cl
0.33
-
)
0.33
-
(MFC in the following) could be a promising candidate to capture the toxic CrO
4
2−
from water, in exchange with the Cl− in an efficient way. The synthesis of this compound might seem simple, consisting of a coprecipitation reaction, and actually, it is strongly affected by the environmental carbon dioxide able to replace the Cl− with the more stable CO
3
2−
. To avoid this problem, LDHs could be also prepared with a rehydration of their calcinated oxide (memory effect). In this work were prepared two samples of MFC: one via coprecipitation (MFC-1 in the following) and one via “memory effect” (MFC-mem in the following). Both the compounds were characterized by means of X-ray powder diffraction (PXRD), Fourier transform infrared spectroscopy (FT-IR) and differential thermal analysis-thermogravimetry (DTA-TG) coupled with evolved gas analysis. The results demonstrated that the synthesis of pure MFC is very difficult, and only a minimum contamination of carbon dioxide led to the formation of the carbonate LDH in a massive way. It was also demonstrated that Mg-Fe LDHs in the presence of carbonate could catalyse the formation of the formic acid (HCOOH) at low temperature (< 300 °C).