Rapid High-Sensitivity
Analysis of Methane Clumped
Isotopes (Δ<sup>13</sup>CH<sub>3</sub>D and Δ<sup>12</sup>CH<sub>2</sub>D<sub>2</sub>) Using Mid-Infrared Laser Spectroscopy
posted on 2025-01-09, 04:29authored byNaizhong Zhang, Ivan Prokhorov, Nico Kueter, Gang Li, Béla Tuzson, Paul M. Magyar, Volker Ebert, Malavika Sivan, Mayuko Nakagawa, Alexis Gilbert, Yuichiro Ueno, Naohiro Yoshida, Thomas Röckmann, Stefano M. Bernasconi, Lukas Emmenegger, Joachim Mohn
Mid-infrared laser absorption spectroscopy enables rapid
and nondestructive
analysis of methane clumped isotopes. However, current analytical
methods require a sample size of 20 mL STP (0.82 mmol) of pure CH<sub>4</sub> gas, which significantly limits its application to natural
samples. To enhance the performance of spectroscopic measurement of
methane clumped isotopes, we established a laser spectroscopic platform
with newly selected spectral windows for clumped isotope analysis:
1076.97 cm<sup>–1</sup> for <sup>12</sup>CH<sub>2</sub>D<sub>2</sub> and 1163.47 cm<sup>–1</sup> for <sup>13</sup>CH<sub>3</sub>D, and a custom-built gas inlet system. These spectral windows
were identified through an extensive spectral survey on newly recorded
high-resolution Fourier transform infrared (FTIR) spectra across the
wavelength range of 870–3220 cm<sup>–1</sup>, thereby
addressing gaps for <sup>12</sup>CH<sub>2</sub>D<sub>2</sub> in existing
spectral databases. In addition, we implemented several key technological
advances, which result in superior control and performance of sample
injection and analysis. We demonstrate that for small samples ranging
from 3 to 10 mL (0.12–0.41 mmol) of CH<sub>4</sub> gas, a measurement
precision comparable to high-resolution isotope ratio mass spectrometry
for Δ<sup>12</sup>CH<sub>2</sub>D<sub>2</sub> (∼1.5‰)
can be achieved through 3 to 8 repetitive measurements using a recycle-refilling
system within a few hours. Samples larger than 10 mL can be quantified
in under 20 min. At the same time, for Δ<sup>13</sup>CH<sub>3</sub>D analysis a repeatability of 0.05‰, superior to mass
spectrometry, was realized. These advancements in reducing sample
size and shortening analysis time significantly improve the practicality
of the spectroscopic technique for determining the clumped isotope
signatures of natural methane samples, particularly for applications
involving low CH<sub>4</sub> concentrations or requiring consecutive
analyses, which are feasible in conjunction with an automated preconcentration
system.