Investigation of Fuel Effects on In-Cylinder Reforming Chemistry using Gas Chromatography.
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Abstract. Aerosols are a source of great uncertainty in radiative forcing predictions and have poorly understood health impacts. Most aerosol mass is formed in the atmosphere from reactive gas-phase organic precursors, forming secondary organic aerosol (SOA). Semivolatile organic compounds (SVOCs) (effective saturation concentration, C*, of 10−1–103 µg m−3) comprise a large fraction of organic aerosol, while intermediate-volatility organic compounds (IVOCs) (C* of 103–106 µg m−3) and volatile organic compounds (VOCs) (C* ≥ 106 µg m−3) are gas-phase precursors to SOA and ozone. The Comprehensive Thermal Desorption Aerosol Gas Chromatograph (cTAG) is the first single instrument simultaneously quantitative for a broad range of compound-specific VOCs, IVOCs and SVOCs. cTAG is a two-channel instrument which measures concentrations of C5–C16 alkane-equivalent-volatility VOCs and IVOCs on one channel and C14–C32 SVOCs on the other coupled to a single high-resolution time-of-flight mass spectrometer, achieving consistent quantification across 15 orders of magnitude of vapor pressure. cTAG obtains concentrations hourly and gas–particle partitioning for SVOCs every other hour, enabling observation of the evolution of these species through oxidation and partitioning into the particle phase. Online derivatization for the SVOC channel enables detection of more polar and oxidized species. In this work we present design details and data evaluating key parameters of instrument performance such as I/VOC collector design optimization, linearity and reproducibility of calibration curves obtained using a custom liquid evaporation system for I/VOCs and the effect of an ozone removal filter on instrument performance. Example timelines of precursors with secondary products are shown, and analysis of a subset of compounds detectable by cTAG demonstrates some of the analytical possibilities with this instrument.
Five modified QuEChERS were tested for the multiresidue analysis of 31 pesticides in rice. Rice was spiked with mixture solution of pesticides at 10 ng/g. Method selection was based on the LODs (sensitivity) and recovery tests (accuracy) of the pesticides. Analysis was done in GC-tandem MS in multiple reaction monitoring mode with a total run time of approximately 37 min. The selected method was validated after spiking rice at 20 and 100 ng/g in rice. The performance characteristics of the method impacted for all selected pesticides were acceptable according to the guidelines for method validation (recovery of 70-120% with an RSD of <20% and r2value of ≥0.99). For rice, matrix effect on the signals of the compounds was corrected by using matrixmatched calibration standards. The LOQs met the requirements of the maximum residue limits for pesticides in rice. The developed method allowed for the simultaneous determination and confirmation of a large number of different groups of pesticides and was fast, simple, inexpensive, and useful for the routine analysis of rice.
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Mass spectrometer techniques for analyzing dilute constituents of mitochondrial suspension
Electronic circuit is used in a paper chromatograph instrument that has excellent sensitivity and furnishes a printed record of each test. The circuit measures and records changes in conductivity in a strip of chromatographic paper as different solutions are placed on it.
Trace amounts of hydrazines in aqueous solutions can be determined by using polythyleneimine /PEI/ in conjunction with the gas chromatographic column. The PEI specifically retains water without altering the separability or elution order of the hydrazine and associated constituents.
Operating parameters and separation of nucleotides on pellicular ion exchangers investigated by liquid chromatographic system
Photoelectric peak generator for repeated reproduction of gas chromatogram peaks while data recording and integration variables are systematically studied
Gas chromatographic resolution of racemic aspartic acid, tryptophan, hydroxy and sulfhydryl amino acids
Gas chromatographic resolution of racemic carbohydrate diastereomers by method used for amino acids
Escherichia coli detection and differentiation from other bacteria by direct gas chromatographic analysis of culture media
Dispersion in gel permeation chromatograph, noting contributions of injection and detection systems to peak broadening and retention time
Gas chromatograph-mass spectrometer combination for in situ analysis of lunar organic matter, describing instrument design and operation
Free stream dispersion without permeation using nonporous glass beads and solutes, examining flow rate, particle size distribution, solute diffusivity, etc
Developing gas-liquid chromatographic method for quantitative analysis of amino acids in blood plasma and urine
Gas-liquid chromatographic separation applied in derivatization chemistry of protein amino acids as N-trimethylsilyl /TMS/ esters
Butyl esters separation from protein amino acids, using acid washed Chromosorb W of various mesh sizes