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Search Publications by: Walter Brent Wilson (Fed)

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Displaying 26 - 50 of 70

Characterization of triacontyl (C-30) liquid chromatographic columns

March 15, 2020
Author(s)
Lane C. Sander, Catherine A. Rimmer, Walter B. Wilson
Differences in the performance characteristics of seventeen commercial C30 liquid chromatographic columns were studied for the separation of carotenoid isomers. A mixture consisting of nine xanthophyll and hydrocarbon carotenoids were separated under

Low-temperature time-resolved phosphorescence excitation emission matrices for the analysis of phenanthro-thiophenes in chromatographic fractions of complex environmental extracts

February 6, 2020
Author(s)
Sadia Arif, Maha Al-Tameemi, Walter Brent Wilson, Stephen Wise, Fernando Barbosa Jr., Andres Campiglia
Polycyclic aromatic sulfur heterocycles (PASHs) are sulfur analogues of polycyclic aromatic hydrocarbons (PAHs) widely found in environmental samples exposed to oil contamination. Despite their potential carcinogenic and mutagenic properties, only few

Certification of Standard Reference Material 3389 Ginsenoside Calibration Solution

May 10, 2019
Author(s)
Walter B. Wilson, Lane C. Sander, Benjamin J. Place, James H. Yen
Standard Reference Material (SRM) 3389 is intended as a calibration solution for use for the determination of ginsenosides in natural matrix samples. A unit of SRM 3389 consists of two different ampule solutions: (1) four ampules of a six-component mixture

Development of a new reversed-phase liquid chromatography and fluorescence method with multichannel selective wavelength detection for the analysis of benzo[a]pyrene and six of its isomers

September 28, 2018
Author(s)
Walter B. Wilson, Stephen A. Wise, Lane C. Sander
The baseline separation of benzo[a]pyrene in complex samples via reversed-phase liquid chromatography (RPLC) is particularly challenging due to the potential for interferences from other molecular mass 252 (MM, g/mol) polycyclic aromatic hydrocarbons (PAHs

Determination of polycyclic aromatic hydrocarbons with molecular mass 302 in standard reference material 1597a by reversed-phase liquid chromatography and stop-flow fluorescence detection

June 21, 2018
Author(s)
Hugh Hayes, Walter Wilson, Lane Sander, Stephen Wise, Andres Campiglia
The identification of isomeric polycyclic aromatic hydrocarbons (PAHs) in complex samples via reversed-phase liquid chromatography (RPLC) with fluorescence detection (FL) is normally based on matching the chromatographic retention times of suspected peaks

Qualitative characterization of three combustion-related standard reference materials for polycyclic aromatic sulfur heterocycles and their alkyl-substituted derivatives via gas chromatography/mass spectrometry

May 7, 2018
Author(s)
Walter Wilson, Hugh Hayes, Andres Campiglia, Stephen Wise
This study represents the most comprehensive qualitative characterization of three combustion- related standard reference materials (SRMs) for polycyclic aromatic sulfur heterocycles (PASHs) and some alkyl-substituted (alkyl-) derivatives to date: SRM

The Influence of the Aromaticity in the Gas Chromatography Retention: The Case of Polycyclic Aromatic Sulfur Heterocycles

December 15, 2017
Author(s)
Jorge O. Ona-Ruales, Yosadara Ruiz-Morales, Fernando Alvarez-Ramirez, Walter Brent Wilson, Stephen A. Wise
The aromaticity has been used as a criterion to explain the GC retention of cata-condensed polycyclic aromatic sulfur heterocycles (PASHs) C12H8S, C16H10S, C20H12S; and peri-condensed PASHs C18H10S, in a GC column with 50% phenyl / 50% methyl silphenylene

Normal-phase liquid chromatography retention behavior of polycyclic aromatic sulfur heterocycles (PASHs) and alkyl-substituted PASH isomers on an aminopropyl stationary phase

December 14, 2017
Author(s)
Walter Wilson, Hugh Hayes, Lane Sander, Andres Campiglia, Stephen Wise
Retention indices for 67 polycyclic aromatic sulfur heterocycles (PASHs) and 80 alkyl- substituted PASHs were determined using normal-phase liquid chromatography (NPLC) on a aminopropyl (NH2) stationary phase. The retention behavior of PASH on the NH2