The consumption of dodecane, a critical flotation collector,
in
the flotation of low-rank coal is particularly high; however, the
adsorption mechanism of dodecane on coal still remains unclear. To
shed light on this issue, the molecular-scale adsorption structure
of dodecane on a lignite surface was investigated in situ by frequency
modulation atomic force microscopy (FM-AFM) for the first time. The
adsorption structure of dodecane on highly oriented pyrolytic graphite
(HOPG) and mica has been detected in advance. Meanwhile, molecular
dynamics (MD) simulations are utilized to elucidate and illustrate
the adsorption structure on HOPG, mica, and lignite. Experimental
results from FM-AFM show that a layered structure of dodecane molecules
is formed on HOPG, while there is no stable adsorption structure on
mica. Meanwhile, a few local monolayer structures of dodecane molecules
are observed on the surface of lignite, and their thickness is approximately
1 nm, which is less than the molecular chain length of dodecane. It
is speculated that the dodecane molecules are adsorbed on lignite
selectively, with the capacity to form a stable adsorption structure.
As indicated by MD simulations, the interaction energy between dodecane
and the mentioned surfaces is in the order HOPG > lignite >
mica.
And the MD simulation results show a desirable match with direct observation
by FM-AFM. In accordance with the characterization of the lignite
sample surface, large amounts of polar oxygen-containing functional
groups may hinder dodecane adsorption behavior. Through in situ molecular
resolution imaging of the interface structure between dodecane and
a raw lignite surface, we provide a new perspective for exploring
the interaction mechanism between nonpolar collectors and a lignite
surface.