Laser desorption
ionization (LDI) mass spectrometry has been widely
applied for the analysis of pitch-related materials. LDI is particularly
useful when samples have very low solubility. However, LDI conditions,
such as laser power output, can have significant impact on the resulting
mass spectra. In this work, we examined the LDI of coronene and two
petroleum pitch samples, a M-50 isotropic pitch and a thermally treated
M-50 pitch that contained a mesophase. LDI at varying laser power
is coupled to ultrahigh-resolution Fourier transform ion cyclotron
resonance mass spectrometry (FT-ICR MS) to determine the impact of
laser power on the elemental compositions of the pitch samples. Coronene
is shown to form large polycyclic aromatic hydrocarbon (PAH) oligomers
at high laser powers. Variations in laser power clearly affect mass
distributions and compound-type distributions of the pitch samples.
The impact of laser power is more significant and visible for the
thermally treated pitch sample, where increased laser power generated
high levels of fully dealkylated (or denuded) polycyclic aromatic
hydrocarbons (dPAHs) and fullerenes. The presence of two types of
PAH ions containing even and odd numbers of hydrogen atoms were observed.
Even-hydrogen-number PAHs are molecular ions produced by direct laser
ionization. The origins of odd-hydrogen-number PAHs are more complicated.
They can result from dealkylation of larger PAHs, protonation of the
parent molecule, and/or ionization of neutral PAH radicals. The latter
can be a significant contributor to the odd-hydrogen-number PAHs.
For analytical applications, a balance in laser power is needed to
vaporize the non-volatile pitch molecules while also minimizing potential
secondary thermal reactions during the LDI process. When laser power
is controlled at a similar level, LDI–MS provides useful information
to understand pitch compositional change from thermal treatment.