Abstract

Closing the carbon (C) and nitrogen (N) balance has yet to be achieved in aerobic bioprocess due to current methodological drawbacks in the frequency of sampling and detection and the challenge in direct measurement of instantaneous N2 emission. To address this issue, a novel system was developed enabling simultaneous and online determination of gaseous C and N species (N2, N2O, NO, NH3, CO2 and CH4) from aerobic composting at a high frequency of 120 times·d−1. A helium‑oxygen gas mixture was used to replace the air in the system to enable direct measurement of N2 emission, and three different gas exchange methods were assessed in their ability to minimize atmospheric background N2: 1) the N2-free gas purging method; 2) one cycle of the evacuation-refilling procedure; 3) one cycle of evacuating and refilling followed by N2-free gas purging. Method 3 was demonstrated as an optimum N2-removal method, and background N2 concentrations decreased to ~66 μmol·mol−1 within 11.6 h. During the N2-free gas purging period, low temperature incubation at 15 °C reduced CO2, CH4, NO, N2O and NH3 losses by 80.5 %, 41-fold, 10-fold, 11,403-fold and 61.4 %, respectively, compared with incubation at 30 °C. Therefore, a fast and low-perturbation N2 removal method was developed, namely the evacuating/refilling-low temperature purging method. Notably, all C and N gases exhibited large within-day variations during the peak emission period, which can be addressed by high-frequency measurement. Based on the developed method, up to 97.8 % of gaseous C and 95.6 % of gaseous N losses were quantified over a 43-day compost incubation, with N2 emission accounting (on average) for 5.8 % of the initial total N. This system for high frequency measurement of multiple gases (including N2) provides a novel tool for obtaining a deeper understanding of C and N turnover and more accurate estimation of reactive N and greenhouse gas emissions during composting.

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