Quantitative real-time in situ measurement of gaseous K, KOH and KCl in a 140 kW entrained-flow biomass gasifier

Abstract

Photofragmentation tunable diode laser absorption spectroscopy (PF-TDLAS) was used to simultaneously measure the concentrations of gas phase atomic potassium (K), potassium hydroxide (KOH) and potassium chloride (KCl) in the reactor core of a 140 kWth atmospheric entrained-flow gasifier (EFG). In two gasification experiments at air-to-fuel equivalence ratio of 0.5, the EFG was first run on forest residues (FR) and then on an 80/20 mixture of FR and wheat straw (FR/WS). Combustion at air-to-fuel equivalence ratio of 1.3 was investigated for comparison. A high K(g) absorbance was observed in gasification, requiring the photofragmentation signals from KOH(g) and KCl(g) to be recorded at a fixed detuning of 7.3 cm−1 from the center of the K(g) absorption profile. In combustion, the fragments recombined instantly after the UV pulse within around 10 µs, whereas in gasification, the K(g) fragment concentration first increased further for 30 µs after the UV pulse, before slowly decaying for up to hundreds of µs. According to 0D reaction kinetics simulations, this could be explained by a difference in recombination kinetics, which is dominated by oxygen reactions in combustion and by hydrogen reactions in gasification. The K species concentrations in the EFG were stable on average, but periodic short-term variations due to fuel feeding were observed, as well as a gradual increase in KOH(g) over the day as the reactor approached global equilibrium. A comparison of the average K species concentrations towards the end of each experiment showed a higher total K in the gas phase for FR/WS, with higher K(g) and KCl(g), but lower KOH(g), compared to the FR fuel. The measured values were in reasonable agreement with predictions by thermodynamic equilibrium calculations.