Detection of trace chlorine pollutants in recycled pulp using gas chromatography–tandem mass spectrometry with response surface–optimized carbon structure online catalysis.

Rationale: Chlorinated aromatics and alkanes are widely used for their flame retardancy, but they need to be monitored when used in recycled pulp. This paper reports the use of palladium acetate/activated carbon (Pa/Ac) activated by nitric acid as an online catalyst to determine chlorinated aromatics and chlorinated alkanes in recycled paper products using gas chromatography–tandem mass spectrometry (GC–MS/MS), which significantly improves the sensitivity of the method and remarkably lowers the detection limits. Methods: The Pa/Ac catalyst was prepared using a self‐made catalytic device and used as key to the online catalytic conversion of target chlorinated aromatic hydrocarbons and chlorinated alkanes for GC–MS/MS analysis. The response surface model was used to optimize catalytic conditions. Then GC–MS/MS in the multireaction monitoring mode with online catalysis was applied for the analysis of polychlorinated biphenyls, polychlorinated terphenyls, polychlorinated naphthalene, and chlorinated paraffins (CP) in recycled paper products. Results: Compared with traditional methods, the Pa/Ac catalyst can transform chlorinated aromatic hydrocarbons into aromatic hydrocarbons through dechlorination hydrogenation, thus lowering the detection limit of the GC–MS/MS method significantly. It can transform paraffin chloride into the corresponding alkane to better distinguish short‐chain, medium‐chain, or long‐chain CPs. Online catalytic conversion significantly improved the sensitivity and reproducibility (88.7%–113.1%) of the method. Tissue samples with various concentration levels of chlorinated aromatics and chlorinated alkanes were tested. The linearity range of the reduced target compounds in the reduction product solution was 0.02–1.00 μg/ml (R2 > 0.995). The quantitative detection limit was 0.03–0.05 μg/kg, and relative standard deviation was less than 6.9%. Conclusion: This study was the first to introduce the Pa/Ac catalytic device as an online catalytic unit in the determination of chlorinated aromatics and chlorinated alkanes using the GC–MS/MS method. The target compounds were converted into alkanes and aromatic hydrocarbons with unchanged carbon structures, and the method could achieve a low detection limit with no need for high‐end methods such as GC‐chemical ionization ion source (CI)‐MS or high‐resolution mass spectrometry. These methods are suitable for the determination of chlorine pollutants in recycled paper and its raw materials. [ABSTRACT FROM AUTHOR]