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Dive into the research topics where David J. Butcher is active.

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Featured researches published by David J. Butcher.


International Journal of Phytoremediation | 2003

Phytoremediation of arsenic and lead in contaminated soil using Chinese brake ferns (Pteris vittata) and Indian mustard (Brassica juncea).

Arthur L. Salido; Kelly L. Hasty; Jae-Min Lim; David J. Butcher

Field and greenhouse experiments were performed to assess the performance of phytoremediation of arsenic and lead from contaminated soil at an EPA Superfund site (Barber Orchard). Chinese Brake ferns (Pteris vittata) were used to extract arsenic. On average, fern shoot arsenic concentrations were as high as 20 times the soil arsenic concentrations under field conditions. It was estimated that 8 years would be required to reduce the acid-extractable portion of soil arsenic to safe levels (40 mg/kg). The effect of soil pH on arsenic extraction was also investigated. Results indicate that increasing soil pH may improve arsenic removal. Indian mustard plants (Brassica juncea) were used under greenhouse conditions to phytoextract soil lead. EDTA was applied to soil and was found to improve lead extraction. When the EDTA concentration was 10 mmol EDTA/kg soil in soil containing 338 mg Pb/kg soil, mustard plants extracted approximately 32 mg of lead. In conclusion, phytoremediation would be a suitable alternative to conventional remediation techniques, especially for soils that do not require immediate remediation.


Analytica Chimica Acta | 2013

Molecular absorption spectrometry in flames and furnaces: a review.

David J. Butcher

Molecular absorption spectrometry (MAS), originally developed in the 1970s, is a technique to determine non-metals in flames and graphite furnaces by monitoring the absorbance of diatomic molecules. Early studies employed low resolution instruments designed for line source atomic absorption, which provided a limited choice of analytical wavelengths, insufficient spectral resolution, and spectral interferences. However, the development of high-resolution continuum source atomic absorption spectrometry (HR-CS AAS) instrumentation has allowed the analysis of challenging samples for non-metals as well as some difficult elements to determine by AAS, such as aluminum and phosphorus. In this review, theory and analytical considerations for MAS are discussed. The principles and limitations of low resolution MAS are described, along with its applications. HR-CS AAS instrumentation is reviewed, emphasizing performance characteristics most relevant for MAS. Applications of flame and HR-CS GFMAS are reviewed, highlighting the most significant work to date. The paper concludes with an evaluation of the enhanced analytical capabilities provided by HR-CS MAS.


Applied Spectroscopy Reviews | 2009

Phytoremediation of Lead in Soil: Recent Applications and Future Prospects

David J. Butcher

Abstract Lead is a very serious contaminant in soil because of its widespread previous application in residential, agricultural, and industrial environments combined with its severe impacts upon human health, particularly upon children. Phytoremediation is a nontraditional approach to remediate contaminated soil involving the use of green plants. Phytostabilization involves the use of plants to stabilize contaminants to reduce human exposure. Phytoextraction involves the use of plants to accumulate contaminants in aboveground shoots, which can be harvested to recycle or discard. Recent phytomediation work has indicated the importance of determining the chemical forms of lead present at a site to develop the most appropriate remediation strategy. Lead phytoextraction typically involves the addition of a chelating agent in order to increase the bioavailability of this contaminant. Because concerns have been raised regarding the persistence of chelating agents in the environment, several research teams have investigated the use biodegradable compounds for this application. It is anticipated that phytoremediation will continue to be a low-cost approach for the remediation of lead in soil.


International Journal of Mass Spectrometry | 1999

Bath gas temperature and the appearance of ion trap tandem mass spectra of high-mass ions

Keiji G. Asano; Douglas E. Goeringer; David J. Butcher; Scott A. McLuckey

Abstract Bath gas temperature effects upon the appearance of ion trap tandem mass spectra of protonated leucine enkephalin have been studied under a variety of ion activation conditions and over a bath gas temperature range of 298–486 K. Bath gas temperature was found to have two possible effects upon the identities and abundances of product ions observed in tandem mass spectra. At high parent ion dissociation rates (>10 s−1) and short activation times ( 10 s−1), relatively long ion activation times (


Applied Spectroscopy Reviews | 2013

Review: Recent Advances in Optical Analytical Atomic Spectrometry

David J. Butcher

Abstract Optical analytical atomic spectrometry includes the techniques of atomic emission, atomic absorption, and atomic fluorescence. In this review, developments in these techniques are reviewed from January 2011 through June 2012, including a summary of applications in various areas of science. The goal is to summarize the most significant recent developments in optical atomic spectrometry.


Journal of Mass Spectrometry | 1999

Effective ion internal temperatures achieved via boundary activation in the quadrupole ion trap: protonated leucine enkephalin

Keiji G. Asano; David J. Butcher; Douglas E. Goeringer; Scott A. McLuckey

The dissociation rate of protonated leucine enkephalin in a quadrupole ion trap was measured as a function of the proximity to which the ions are brought to a stability boundary. A bath gas temperature of 480 K was used so that a dissociation rate could be readily measured even when the parent ions were remote from a stability boundary. Changes in the dissociation rate as a function of d.c. potential applied to the ring electrode of the ion trap, used to bring ions close to a stability boundary, could then be attributed to the ‘boundary activation’ process. A relationship between dissociation rate and parent ion effective internal temperature, derived from a study involving conventional ion trap resonance excitation, was used to estimate effective ion internal temperatures achieved under the boundary activation conditions used here. Effective ion internal temperatures 170 K above the bath gas temperature could readily be achieved using boundary activation. However, the efficiency of the overall boundary activation experiment was compromised by an initial rapid parent ion loss that occurred upon application of the d.c. potential. After correction for this initial ion loss, dissociation rates and relatively low ion ejection rates could be measured. Effective ion internal temperatures achieved with boundary activation are similar to those observed previously using conventional resonance excitation. However, the generally poorer efficiencies associated with boundary activation that are observed with resonance excitation at high dissociation rates suggests that higher ion internal temperatures can be achieved with conventional resonance excitation. Copyright


Applied Spectroscopy Reviews | 2006

Advances in Electrothermal Atomization Atomic Absorption Spectrometry: Instrumentation, Methods, and Applications

David J. Butcher

Abstract Electrothermal atomization (ETA) atomic absorption spectrometry (AAS) offers high sensitivity quantitative analysis of a wide variety of samples for metals. Following an introduction to this instrumental method, recent developments in instrumentation, methods of sample preparation, and significant applications are reviewed, illustrating significant developments. The focus of this review is on the practical application of ETA‐AAS for real sample analysis.


Microchemical Journal | 2000

Solid phase microextraction for the determination of volatile organics in the foliage of Fraser fir (Abies fraseri)

Delton A Vereen; J.Paul McCall; David J. Butcher

Solid phase micro extraction (SPME) was investigated for the determination of volatile chemicals in the foliage of Fraser fir (Abies fraseri). Advantages of SPME include its speed, sensitivity, and ability to determine volatiles without chemical solvents. In this study, qualitative comparisons were performed of the volatiles emitted from living foliage (in situ), damaged living foliage (in situ damaged), and severed foliage (ex situ). These studies suggest that β-phellandrene and γ-terpinene may be emitted as a response to foliar injury. Comparisons were made of the volatiles collected by SPME with ex situ sampling to previous studies in our laboratory using methylene chloride extraction. Similar results were obtained by the two extraction methods.


Microchemical Journal | 2000

The real-time analysis of gases by direct sampling-mass spectrometry : elemental and molecular applications

David J. Butcher

Real-time analysis of gases for volatile organic compounds or elements is required for a number of applications. Direct sampling-mass spectrometry (DS-MS) is one approach to solve these analytical problems. This article reviews various instrumental configurations and applications of DS-MS. Inlet systems employed for DS-MS include membranes, microtrap interfaces, atmospheric sampling glow discharge ionization, atmospheric pressure ionization, microwave plasma ionization, and capillary restrictors. The use of laser-based ionization methods for DS-MS is described, including resonance-enhanced multiphoton ionization and single photon ionization.


Instrumentation Science & Technology | 2010

ADVANCES IN INDUCTIVELY COUPLED PLASMA OPTICAL EMISSION SPECTROMETRY FOR ENVIRONMENTAL ANALYSIS

David J. Butcher

Inductively coupled plasma optical emission spectrometry (ICP-OES) is a widely used method of elemental analysis because of its excellent analytical figures of merit and relative freedom from interferences. This review considers recent relative reviews, fundamental studies of the inductively coupled plasma, advances in other atom cells for atomic emission, and preconcentration methods. The focus of the article is on recent applications, illustrating the versatility of the instrumentation for practical analysis.

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Royce S. Woosley

Western Carolina University

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K.G. Vandervoort

Argonne National Laboratory

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Douglas E. Goeringer

Oak Ridge National Laboratory

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Keiji G. Asano

Oak Ridge National Laboratory

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Arthur L. Salido

Western Carolina University

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Michael R. Shepard

Western Carolina University

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Alisha Pendergrass

Western Carolina University

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Jae-Min Lim

Western Carolina University

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A.Jason Fowlkes

Western Carolina University

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