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[Display omitted] • UDB and DB at different pyrolysis temperatures played contrasting roles. • DB800-amended group displayed superior nitrogen removal performance. • DB at lower pyrolysis temperature imposed suppression. • Properties of dissolved organic matter released by DB were tracked at molecular level. Biochar has attracted increasingly attention in the biological wastewater treatment owing to its unique environmental behavior. However, the differential effects of undissolved and dissolved fractions of biochar (hereafter named as UDB and DB, respectively) on the anaerobic ammonium oxidation (anammox) process remain unclear. The study evaluated the nitrogen removal performance of anammox system in response to UDB and DB prepared at different pyrolysis temperatures (300 °C, 550 °C and 800 °C). The DB800-amended group displayed superior nitrogen removal performance with the total nitrogen removal efficiency (TNRE) of 92.8 ± 1.4 %. Compared with CK, TNRE was changed by +5.0 % (UDB300), +0.4 % (UDB550) and −22.3 % (UDB800) for UDB-amended groups, and by −16.0 % (DB300), −9.4 % (DB550), and +9.2 % (DB800) for DB-amended groups, respectively. The differences were closely related to the physicochemical properties of UDB and DB. Particularly, dissolved organic matter released by DB were tracked at molecular level, which revealed that CHO occupied the highest proportion of 70.3 % and lignin-like and carboxylic rich alicyclic molecules were dominant in DB800. This study would facilitate the understanding of the differences between the nitrogen removal performance of UDB and DB-amended anammox, thus providing deeper insights for the comprehensive assessment of the impacts of biochar on the anammox process. [ABSTRACT FROM AUTHOR]

[Display omitted] • Electro-oxidation of N-heterocycles produces N 2 , N H 3 / N H 4 + , N O 3 - , C O and C O 2. • N H 3 / N H 4 + and an apparent N 2 yield correlate linearly with carbon removal. • Both apparent N 2 and N O 3 - form directly from organic intermediates rather than N H 3 / N H 4 +. • Higher concentrations of parent compounds promote a higher apparent N 2 selectivity. • N O 3 - dominates when oxidation of carbon is mass transfer-limited or at basic pH. We report for the first time the carbon and nitrogen product distribution during the electrochemical oxidation (EO) of pyrazine and related N-heterocyclic compounds (NHCs) present in the hard-to-treat wastewater from a biofuel production process. The experimental study was carried out using a boron-doped diamond anode. Identified and quantified intermediate products included oxamic acid, formamide, oxalic acid, and formic acid. Analysis of the C and N yields as a function of the extent of carbon removal reveals the influence of the current- and mass transfer-control operating regimes on product distribution. Carbon monoxide, which was detected among the gaseous products, suggests a possible decarbonylation pathway in the current-controlled regime. An apparent nitrogen gas and ammonium yields correlated linearly with the carbon removal, while nitrate yields significantly increased in the mass transfer-controlled regime. Nitrate and apparent nitrogen gas appear to form directly from organic nitrogen intermediates, rather than from the ammonium that also forms in the process. The research gives new insights into the NHCs degradation pathways, product distribution, and final water composition as a function of operating regime in the EO of recalcitrant wastewater. [ABSTRACT FROM AUTHOR]