Position-Specific Isotope Analysis of Propane by Mid-IR Laser Absorption Spectroscopy.

Intramolecular or position-specific carbon isotope analysis of propane (13CH3-12CH2-12CH3 and 12CH3-13CH2-12CH3) provides unique insights into its formation mechanism and temperature history. The unambiguous detection of such carbon isotopic distributions with currently established methods is challenging due to the complexity of the technique and the tedious sample preparation. We present a direct and nondestructive analytical technique to quantify the two singly substituted, terminal (13Ct) and central (13Cc), propane isotopomers, based on quantum cascade laser absorption spectroscopy. The required spectral information on the propane isotopomers was first obtained using a high-resolution Fourier-transform infrared (FTIR) spectrometer and then used to select suitable mid-infrared regions with minimal spectral interference to obtain the optimum sensitivity and selectivity. We then measured high-resolution spectra around 1384 cm-1 of both singly substituted isotopomers by mid-IR quantum cascade laser absorption spectroscopy using a Stirling-cooled segmented circular multipass cell (SC-MPC). The spectra of the pure propane isotopomers were acquired at both 300 and 155 K and served as spectral templates to quantify samples with different levels of 13C at the central (c) and terminal (t) positions. A prerequisite for the precision using this reference template fitting method is a good match of amount fraction and pressure between the sample and templates. For samples at natural abundance, we achieved a precision of 0.33 ‰ for δ13Ct and 0.73 ‰ for δ13Cc values within 100 s integration time. This is the first demonstration of site-specific high-precision measurements of isotopically substituted non-methane hydrocarbons using laser absorption spectroscopy. The versatility of this analytical approach may open up new opportunities for the study of isotopic distribution of other organic compounds.

Quantum cascade laser absorption spectrometer with a low temperature multipass cell for precision clumped CO2 measurement.

We present a quantum cascade laser-based absorption spectrometer deploying a compact (145 mL volume) segmented circular multipass cell (SC-MPC) with 6 m optical path length. This SC-MPC is embedded into an effective cooling system to facilitate operation at cryogenic temperatures. For CO2, the sample is cooled to 153 K, i.e. close to the sublimation point at 10 mbar. This enables efficient suppression of interfering hot-band transitions of the more abundant isotopic species and thereby enhances analytical precision. As a demonstration, the amount fractions of all three CO2 isotopologues involved in the kinetic isotope exchange reaction of 12C16O2 + 12C18O2⇌ 2·12C16O18O are measured. The precision in the ratios [12C18O2]/[12C16O2] and [12C16O18O]/[12C16O2] is 0.05 ‰ with 25 s integration time. In addition, we determine the variation of the equilibrium constant, K, of the above exchange reaction for carbon-dioxide samples equilibrated at 300 K and 1273 K, respectively.

High-resolution and gapless dual comb spectroscopy with current-tuned quantum cascade lasers.

We present gapless, high-resolution absorption and dispersion spectra obtained with quantum cascade laser frequency combs covering 55 cm-1. Using phase-sensitive dual comb design, the comb lines are gradually swept over 10 GHz, corresponding to the free spectral range of the laser devices, by applying a current modulation. We show that with interleaving the spectral point spacing is reduced by more than four orders of magnitude over the full spectral span of the frequency comb. The potential of this technique for high-precision gas sensing is illustrated by measuring the low pressure (107 hPa) absorption and dispersion spectra of methane spanning the range of 1170 cm-1 - 1225 cm-1 with a resolution of 0.001 cm-1.