The effects of thermal boundary layers on tunable diode laser absorption spectroscopy (TDLAS) measurement results must be quantified when using the line-of-sight (LOS) TDLAS under conditions with spatial temperature gradient. In this paper, a new methodology based on spectral simulation is presented quantifying the LOS TDLAS measurement deviation under conditions with thermal boundary layers. The effects of different temperature gradients and thermal boundary layer thickness on spectral collisional widths and gas concentration measurements are quantified. A CO ₂ TDLAS spectrometer, which has two gas cells to generate the spatial temperature gradients, was employed to validate the simulation results. The measured deviations and LOS averaged collisional widths are in very good agreement with the simulated results for conditions with different temperature gradients. We demonstrate quantification of thermal boundary layers’ thickness with proposed method by exploitation of the LOS averaged the collisional width of the path-integrated spectrum.

This work presents a mid-IR direct tunable diode laser absorption spectroscopy (dTDLAS)-based HCl spectrometer, which is specially designed and optimized to measure HCl concentration in combustion exhaust gas matrices (i.e. elevated gas temperatures, high water vapour and CO₂ contents). The work is motivated by (legal) requirements for monitoring combustion emissions from large-scale power stations or biomass burning domestic boilers. In our novel dTDLAS HCl spectrometer we use a low power room temperature mid-IR ICL diode laser to access the HCl P5 line at 2775.76 cm⁻¹ in the 1-0 vibrational band which was especially selected for gas matrixes with high CO₂ and H₂O admixtures. With this set-up we demonstrate at 77 cm path length, total pressure from 320 hPa to 954 hPa, room temperature and at 110 s of signal averaging an optimal precision of 0.17 µmol/mol (ppm). Gas monitoring in combustion applications and elevated gas temperatures are prone to systematic errors caused by spectroscopic falsifications in colder gas boundary layers (BL) unavoidable in the high temperature gas ducts. These BL lead, e.g. to temperature, matrix composition or target gas concentration gradients near walls, which also influence the spectroscopic raw signal via their temperature and collision partner dependence. Depending on the chosen spectral line these can cause significant systematic deviations in in-situ, line-of-sight (LOS) laser spectrometers. For an improved understanding of the quantitative effects of thermal BL on our LOS HCl dTDLAS spectrometer and better representing real BL, we expanded our spectroscopic BL simulation model to allow for continuous (linear) instead of the previous stepwise changes. From the new simulation results, we deduce systematic relative deviations in the extracted HCl-concentration to be up to 10% depending on the magnitude of the BL changes and the choice of the “representative” single temperature measurement. With this simulation model, a user can now derive the system’s systematic deviation based on assumptions on the present temperature gradients. The model also helps the user to choose the gas temperature measurement location in his process, in order to minimize the spatial heterogeneity effects.

Potassium (K) is one of the main and most hazardous trace species released to the gas-phase during thermochemical conversion of biomass. Accurate experimental data and models of K release are needed to better understand the chemistry involved. Tunable diode laser absorption spectroscopy (TDLAS) is used for simultaneous real-time in situ measurements of gas-phase atomic K, water (H₂O) and gas temperature in the vicinity (boundary layer) of biomass particles during combustion in a laboratory single-particle reactor. Atomic K is detected in a wide dynamic range, including optically thick conditions, using direct absorption spectroscopy at the wavelength of 770 nm, while H₂O and temperature are determined by calibration-free scanned wavelength modulation spectroscopy at 1398 nm. The high accuracy and repeatability of the setup allows to distinguish measurements with varying initial particle mass, laser beam height above the particle and fuel type. Four types of biomass with different ash composition are investigated: softwood, Salix, Miscanthus and wheat straw. For Salix and wheat straw, the K release behaviour is, for the first time, compared to a detailed numerical particle model taking into account the interaction between K/S/Cl composition in the particle ash. A good agreement is achieved between the measured and calculated time-resolved atomic K concentrations for the devolatilization phase of the biomass particles.