A novel thermochemical
process based on a single step was optimized
to obtain magnetic activated carbons from an industrial biomass waste.
Anhydrous iron chloride was used as an activating agent and mixed
directly with the chestnut shell waste. The effect of the activation
temperature (220–800 °C) on the chemical, morphological,
textural, and magnetic properties of the materials was studied. The
results demonstrated the presence of different iron compounds depending
on the activation temperature set as well as their influence on morphological
and textural development of the magnetic activated carbons (BET specific
surface area, S
BET, up to 568 m2 g–1, total pore volume, V
TOT, up to 0.294 cm3 g–1 vs 1
m2 g–1 and 0.007 cm3 g–1, respectively, for the raw biomass waste). The techniques
employed, especially Mössbauer spectroscopy, showed relative
contributions of the different iron compounds (magnetite, maghemite,
metallic iron, and so on) in the materials. The higher activation
temperature (800 °C) favored the formation of metal Fe and iron
carbide. Additionally, the magnetic properties measured by vibrating
sample magnetometry confirmed the coexistence of different ferromagnetic
phases with the remanent magnetization, M
R, (up to 3.88 emu/g) and coercivity, H
c, (up to 140 Oe), being larger as the activation temperature increases.
A higher activation temperature favored the development and evolution
toward other iron compounds, while at low temperature, 220 °C,
the presence of these compounds were null, and their behavior resembled
the results obtained for the original biomass waste.