Soil micro- and nanoplastic contamination is escalating globally, yet its potential to interfere with routine agrochemical analyses remains poorly quantified. Standard operating procedures (SOPs) were calibrated for natural soil matrices and may not account for synthetic, carbon-rich polymers. This controlled model study quantified the analytical sensitivity of FAO/GLOSOLAN/ISO standard procedures to polystyrene nanoparticle (50 nm) contamination across a 0–0.5% (w/w) gradient in a Luvic Chernozem. Key parameters—pH, soil carbon, total nitrogen (TN), cation exchange capacity (CEC), and clay fraction—were measured following standardized protocols. The Walkley–Black method exhibited a strong dose-dependent increase in measured SOC (r = 0.93), reflecting systematic overestimation due to dichromate co-oxidation of polymer matrix, likely facilitated by exothermic heating above polystyrene’s glass transition temperature. The Dumas method showed moderate correlation (r = 0.59) but higher replicate variability driven by small aliquot size and heterogeneous nanoparticle distribution. The pH measurements displayed non-linear responses and elevated variability at low doses, whereas TN, CEC, and clay content remained statistically stable. These findings demonstrate that nanoplastic contamination can introduce significant analytical artifacts in oxidation-based SOC determinations, potentially leading to misinterpretation of soil carbon trends. Given the single-soil, single-polymer design, results represent a system-specific proof of analytical vulnerability rather than a universally quantified bias. Laboratories analyzing potentially contaminated soils should exercise caution with wet-oxidation SOC data, and broader SOP revisions must await multi-soil, multi-polymer validation campaigns.
Nizamutdinov et al. (Thu,) studied this question.