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Catherine L. Arthur

Bio: Catherine L. Arthur is an academic researcher from University of Waterloo. The author has contributed to research in topics: Solid-phase microextraction & Sample preparation. The author has an hindex of 9, co-authored 9 publications receiving 5936 citations.

Papers
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Journal ArticleDOI
TL;DR: The solid phase microextraction (SPME) technique as mentioned in this paper involves exposing a fused silica fiber that has been coated with a stationary phase to and aqueous solution containing organic contaminants.
Abstract: The solid-phase microextraction (SPME) technique involves exposing a fused silica fiber that has been coated with a stationary phase to and aqueous solution containing organic contaminants. The analytes partition into the stationary phase until an equilibrium has been reached, after which the fiber is removed from the solution and the analytes are thermally desorbed in the injector of a gas chromatograph

598 citations

Journal ArticleDOI
TL;DR: In this paper, Solid Phase Microextraction (SPME) was applied to the analysis of benzene, toluene, ethyl benzene and xylenes in groundwater.
Abstract: rn Solid-phase microextraction (SPME) is applied to the analysis of benzene, toluene, ethyl benzene, and xylenes in groundwater. The inexpensive SPME method reduced the sample preparation time by 3-7-fold when compared to purge and trap methods. The relative standard deviation ranged from 3 to 5% for the single-operator relative standard deviation using a methyl silicone fiber. Limits of detection of 1-3 ppb (w/v) were obtained when using a fiber coated with 56-pm methyl silicone film and FID detection. The linear range extended from 15 to 3000 ppb (w/v). Solvents have been completely removed from the sample preparation step.

258 citations

Journal ArticleDOI
TL;DR: The objective of the current protocol is to provide a detailed sequence of S PME optimization steps that can be applied toward development of SPME methods for a wide range of analytical applications.
Abstract: Solid-phase microextraction (SPME) is a sample preparation method developed to solve some of the analytical challenges of sample preparation as well as sample introduction and integration of different analytical steps into one system. Since its development, the utilization of SPME has addressed the need to facilitate rapid sample preparation and integrate sampling, extraction, concentration and sample introduction to an analytical instrument into one solvent-free step. This achievement resulted in fast adoption of the technique in many fields of analytical chemistry and successful hyphenation to continuously developing sophisticated separation and detection systems. However, the facilitation of high-quality analytical methods in combination with SPME requires optimization of the parameters that affect the extraction efficiency of this sample preparation method. Therefore, the objective of the current protocol is to provide a detailed sequence of SPME optimization steps that can be applied toward development of SPME methods for a wide range of analytical applications.

251 citations

Journal ArticleDOI
TL;DR: The potential of the microextraction technique for the analysis of flavor and fragrance compounds in non-caffeinated beverages is demonstrated, and no solvents or class-fractionation steps are required and the method has good potential for automation.

186 citations


Cited by
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Journal ArticleDOI
TL;DR: The ability of DLLME technique in the extraction of other organic compounds such as organochlorine pesticides, organophosphorus pesticides and substituted benzene compounds were studied.

2,959 citations

Journal ArticleDOI
TL;DR: This work proposes to comprehensively review the recent advances in molecular imprinting including versatile perspectives and applications, concerning novel preparation technologies and strategies of MIT, and highlight the applications of MIPs.
Abstract: Molecular imprinting technology (MIT), often described as a method of making a molecular lock to match a molecular key, is a technique for the creation of molecularly imprinted polymers (MIPs) with tailor-made binding sites complementary to the template molecules in shape, size and functional groups. Owing to their unique features of structure predictability, recognition specificity and application universality, MIPs have found a wide range of applications in various fields. Herein, we propose to comprehensively review the recent advances in molecular imprinting including versatile perspectives and applications, concerning novel preparation technologies and strategies of MIT, and highlight the applications of MIPs. The fundamentals of MIPs involving essential elements, preparation procedures and characterization methods are briefly outlined. Smart MIT for MIPs is especially highlighted including ingenious MIT (surface imprinting, nanoimprinting, etc.), special strategies of MIT (dummy imprinting, segment imprinting, etc.) and stimuli-responsive MIT (single/dual/multi-responsive technology). By virtue of smart MIT, new formatted MIPs gain popularity for versatile applications, including sample pretreatment/chromatographic separation (solid phase extraction, monolithic column chromatography, etc.) and chemical/biological sensing (electrochemical sensing, fluorescence sensing, etc.). Finally, we propose the remaining challenges and future perspectives to accelerate the development of MIT, and to utilize it for further developing versatile MIPs with a wide range of applications (650 references).

1,647 citations

Journal ArticleDOI
TL;DR: The theory and practice of a novel approach for sample enrichment, namely the application of stir bars coated with the sorbent polydimethylsiloxane (PDMS) and referred to as stir bar sorptive extraction (SBSE) are presented in this paper.
Abstract: The theory and practice of a novel approach for sample enrichment, namely the application of stir bars coated with the sorbent polydimethylsiloxane (PDMS) and referred to as stir bar sorptive extraction (SBSE) are presented. Stir bars with a length of 10 and 40 mm coated with 55 and 219 μL of PDMS liquid phase, respectively were applied. The 10-mm stir bars are best suited for stirring sample volumes from 10 up to 50 mL whereas 40-mm stir bars are more ideal for sample volumes up to 250 mL. Depending on sample volume and the stirring speed, typical stirring times for equilibration are between 30 and 60 min. The performance of SBSE is illustrated with the analysis of volatile and semivolatile micropollutants from aqueous samples. Detection limits using mass selective detection are in the low ng/L range for a wide selection of analytes from the EPA priority pollutant lists including analytes ranging in volatility from 1,1,1-trichloroethane to chrysene. For the extraction of selected compounds from 200-mL samples, detection limits below 0.1 ng/L are reached in the selected ion monitoring mode. A comparison between SBSE and solid-phase microextraction is made. ©1999 John Wiley & Sons, Inc. J Micro Sep 11: 737–747, 1999

1,362 citations

Journal ArticleDOI
TL;DR: An analytical technique is described which combines solvent extraction with gas chromatographic (GC) analysis in a simple and inexpensive apparatus involving very little solvent consumption and is in good agreement with a convective-diffusive kinetic model.
Abstract: An analytical technique is described which combines solvent extraction with gas chromatographic (GC) analysis in a simple and inexpensive apparatus involving very little solvent consumption. A small drop (8 μL) of a water-immiscible organic solvent, containing an internal standard, is located at the end of a Teflon rod which is immersed in a stirred aqueous sample solution. After the solution has been stirred for a prescribed period of time, the probe is withdrawn from the aqueous solution, and the organic phase is sampled with a microsyringe and injected into the GC for quantification. The observed rate of solvent extraction is in good agreement with a convective−diffusive kinetic model. Analytically, the relative standard deviation of the method is 1.7% for a 5.00-min extraction of the analyte 4-methylacetophenone into n-octane.

1,191 citations

Journal ArticleDOI
TL;DR: In this article, a modification of the solid-phase microextraction method (SPME) is proposed to shortens the time of extraction and facilitates the application of this method to analysis of solid samples.
Abstract: Headspace solid-phase microextraction is a solvent-free sample preparation technique in which a fused silica fiber coated with polymeric organic liquid is introduced into the headspace above the sample. The volatilized organic analytes are extracted and concentrated in the coating and then transferred to the analytical instrument for desorption and analysis. This modification of the solid-phase microextraction method (SPME) shortens the time of extraction and facilitates the application of this method to analysis of solid samples. The detection limits of the headspace SPME technique are at ppt level when ion trap mass spectrometry is used as the detector and are very similar to that of the direct SPME technique

1,157 citations