A sensitive gas chromatographic method was developed to monitor the reaction of lithium diisopropylamide (LDA) with dimethyl methylphosphonate (DMMP) to generate the phosphonate carbanion (DMMPA). Analysis of the DMMPA was complicated due to its thermal instability and lack of a chromophore. To overcome these problems, samples were derivatized with trimethylsilylchloride (TMSCI) to form DMMPA-TMS which was sufficiently volatile and thermally stable for GC analysis. Work-up of the derivatized solution with 10 vol.% 2-propanol in hexanes was necessary to quench residual TMSCI prior to GC analysis. The presence of DMMPA-TMS and other sample components was confirmed by GC-MS analysis. This method was utilized to profile the synthesis of DMMPA as DMMP was added to LDA and then aged at -78 degrees C. Method precision for DMMPA-TMS of less than 0.2% RSD was achieved for repeat injections after normalization of the response with n-dodecane contained in the sample. Due to the thermal instability of the DMMPA, subambient derivatization temperatures were essential to the stability, and consequently, accurate quantification. Under optimized conditions, this derivatization was successfully utilized as a process monitoring tool.
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http://dx.doi.org/10.1016/s0021-9673(02)01305-5 | DOI Listing |
Analyst
January 2025
School of Mechanical and Electrical Engineering, Soochow University, Suzhou, 215021, China.
A portable gas chromatograph-mass spectrometer (GC-MS) is an effective instrument for rapid on-site detection of volatile organic compounds (VOCs). Current instruments typically adsorb samples at ambient temperature, challenging the detection of low-boiling VOCs. In this study, a low-temperature adsorption thermal desorption method is proposed for sample enrichment in a portable GC-MS.
View Article and Find Full Text PDFJ Sep Sci
January 2025
Department of Analytical, Bioanalytical Sciences and Miniaturization (LSABM) Chemistry, Biology and Innovation (CBI), UMR CNRS-ESPCI Paris 8231, ESPCI Paris, PSL University, CNRS, Paris, France.
Adduction on protein nucleophile sites by mustard agents can be monitored to assess detection of retrospective exposure to these agents. Cysteine 34 (Cys34) on human serum albumin was selected as the target of choice. This work targets di- and tripeptides adducted on Cys34 by sulfur mustard, sesquimustard, and nitrogen mustards separated in hydrophilic liquid chromatography (HILIC) and Reversed-Phase (RP) mode.
View Article and Find Full Text PDFChemosphere
December 2024
Department of Civil, Urban, Earth, and Environmental Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan, 44919, Republic of Korea. Electronic address:
Pine needle, pine bark, and soil samples were collected from various regions in South Korea, considering the suitability of vegetation samples as passive samplers. A total of 27 organochlorine pesticides (OCPs) were analyzed using a gas chromatograph/high-resolution mass spectrometer (GC/HRMS). The total concentrations of OCPs ranged between 650 and 3652 pg/g dw in soil, 215 and 1384 pg/g ww in pine needles, and 456 and 1723 pg/g ww in pine bark.
View Article and Find Full Text PDFJ Chromatogr A
December 2024
School of Energy and Power Engineering, University of Shanghai for Science and Technology, Shanghai 200093, China. Electronic address:
The evolution of precursors to form secondary organic aerosol (SOA) is still a challenge in atmospheric chemistry. Chamber experiments were conducted to simulate the ambient OH oxidation of naphthalene and α-pinene, which are typical markers of anthropogenic and biogenic emissions. Particulate matters were sampled by quartz filters and were analyzed by comprehensive two-dimensional gas chromatography (GC×GC) coupled with a thermal desorption system (TD) and a mass spectrometer (MS).
View Article and Find Full Text PDFPDA J Pharm Sci Technol
December 2024
Nelson Labs, Romeinsestraat 12, 3001 Heverlee, Belgium.
Leachables in drug products and from medical devices can adversely affect patient health and thus must be identified and quantified. Accurate and protective quantitation in target analysis for leachables (and extractables as potential leachables) is accomplished via compound-specific calibration curves. Quantification in non-targeted analysis (NTA) is complicated by the variable relative response factors (RRFs) among and between individual leachables and the circumstance that the leachables are not known until the NTA is completed.
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