High speed polarity switching MS/MS applied to polymer additives analysis
Posters | 2011 | ShimadzuInstrumentation
Polymer additives are essential for tuning material performance, safety and cost across diverse applications such as plastics, fibers, elastomers and lubricants. As formulations grow more complex, rapid and reliable identification of additives becomes critical for quality control, competitive benchmarking and safety assessments.
This work presents a high-speed LC-MS/MS screening method for polymer additives leveraging ultra-fast polarity switching and synchronized survey scanning. The goal was to detect both molecular ions and characteristic fragments of multiple additives in a single run and to apply the method to real plastic laminate samples.
Standard mixtures containing 12 representative polymer additives were prepared in methanol. Plastic laminates were extracted with tetrahydrofuran under ultrasonication, diluted with ammonium acetate solution and filtered. Samples underwent UHPLC separation on a C18 column with a formic acid/methanol gradient, followed by MS/MS analysis using alternating positive/negative Q3 scans and product ion scans at low and high collision energies within a 400 ms cycle.
All twelve additives in the standard were detected in one acquisition, with clear Q3 full scans and MS/MS spectra at 20 V and 40 V collision energies in both polarities. In plastic laminate extracts, three additives (Tinuvin P, Irganox 245 and Cyanox 425) were unambiguously identified. Additional chromatographic peaks indicated the presence of unknown compounds, highlighting the screening method’s diagnostic power.
The ultra-fast polarity switching workflow delivers comprehensive qualitative data in a single run, greatly enhancing throughput for routine QA/QC, formulation development and competitive product analysis. The rich MS/MS information supports confident identification even in complex mixtures.
Integration with high-resolution mass spectrometry and advanced data analytics could enable trace-level identification and structural elucidation of novel additives and degradation products. Real-time monitoring during polymer processing and environmental screening of microplastic additives represent promising extensions.
The developed high-speed LC-MS/MS method with synchronized survey scanning provides a powerful, efficient platform for polymer additive analysis, combining rapid multi-polarity acquisition with detailed MS/MS profiling to support a wide range of research and industrial applications.
LC/MS, LC/MS/MS, LC/QQQ
IndustriesEnergy & Chemicals
ManufacturerShimadzu
Summary
Significance of the topic
Polymer additives are essential for tuning material performance, safety and cost across diverse applications such as plastics, fibers, elastomers and lubricants. As formulations grow more complex, rapid and reliable identification of additives becomes critical for quality control, competitive benchmarking and safety assessments.
Objectives and overview
This work presents a high-speed LC-MS/MS screening method for polymer additives leveraging ultra-fast polarity switching and synchronized survey scanning. The goal was to detect both molecular ions and characteristic fragments of multiple additives in a single run and to apply the method to real plastic laminate samples.
Methodology
Standard mixtures containing 12 representative polymer additives were prepared in methanol. Plastic laminates were extracted with tetrahydrofuran under ultrasonication, diluted with ammonium acetate solution and filtered. Samples underwent UHPLC separation on a C18 column with a formic acid/methanol gradient, followed by MS/MS analysis using alternating positive/negative Q3 scans and product ion scans at low and high collision energies within a 400 ms cycle.
Instrumentation used
- Shimadzu LCMS-8030 triple quadrupole mass spectrometer with 15 ms polarity switching and 15 000 u/sec scan speed
- Synchronized Survey Scan function triggering dependent product ion scans in multi-polarity
- Shimadzu Nexera UHPLC system with Shim-pack XR-ODS2 column (75 × 2.0 mm, 2.2 µm)
Main results and discussion
All twelve additives in the standard were detected in one acquisition, with clear Q3 full scans and MS/MS spectra at 20 V and 40 V collision energies in both polarities. In plastic laminate extracts, three additives (Tinuvin P, Irganox 245 and Cyanox 425) were unambiguously identified. Additional chromatographic peaks indicated the presence of unknown compounds, highlighting the screening method’s diagnostic power.
Benefits and practical applications
The ultra-fast polarity switching workflow delivers comprehensive qualitative data in a single run, greatly enhancing throughput for routine QA/QC, formulation development and competitive product analysis. The rich MS/MS information supports confident identification even in complex mixtures.
Future trends and potential applications
Integration with high-resolution mass spectrometry and advanced data analytics could enable trace-level identification and structural elucidation of novel additives and degradation products. Real-time monitoring during polymer processing and environmental screening of microplastic additives represent promising extensions.
Conclusion
The developed high-speed LC-MS/MS method with synchronized survey scanning provides a powerful, efficient platform for polymer additive analysis, combining rapid multi-polarity acquisition with detailed MS/MS profiling to support a wide range of research and industrial applications.
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