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Dive into the research topics where James H. Buchanan is active.

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Featured researches published by James H. Buchanan.


Chemistry: A European Journal | 2017

Postsynthetic Incorporation of a Singlet Oxygen Photosensitizer in a Metal-Organic Framework for Fast and Selective Oxidative Detoxification of Sulfur Mustard

Ashlee J. Howarth; Cassandra T. Buru; Yangyang Liu; Ann M. Ploskonka; Karel J. Hartlieb; Monica McEntee; John J. Mahle; James H. Buchanan; Erin M. Durke; Salih S. Al-Juaid; J. Fraser Stoddart; Jared B. DeCoste; Joseph T. Hupp; Omar K. Farha

A fullerene-based photosensitizer is incorporated postsynthetically into a Zr6 -based MOF, NU-1000, for enhanced singlet oxygen production. The structural organic linkers in the MOF platform also act as photosensitizers which contribute to the overall generation of singlet oxygen from the material under UV irradiation. The singlet oxygen generated by the MOF/fullerene material is shown to oxidize sulfur mustard selectively to the less toxic bis(2-chloroethyl)sulfoxide with a half-life of only 11 min.


Langmuir | 2013

Mass Transfer and Adsorption Equilibrium for Low Volatility Alkanes in BPL Activated Carbon

Yu Wang; John J. Mahle; Amanda M. B. Furtado; T. Grant Glover; James H. Buchanan; Gregory W. Peterson; M. Douglas LeVan

The structure of a molecule and its concentration can strongly influence diffusional properties for transport in nanoporous materials. We study mass transfer of alkanes in BPL activated carbon using the concentration-swing frequency response method, which can easily discriminate among mass transfer mechanisms. We measure concentration-dependent diffusion rates for n-hexane, n-octane, n-decane, 2,7-dimethyloctane, and cyclodecane, which have different carbon numbers and geometries: straight chain, branched chain, and cyclic. Micropore diffusion is determined to be the controlling mass transfer resistance except at low relative saturation for n-decane, where an external mass transfer resistance also becomes important, showing that the controlling mass transfer mechanism can change with system concentration. Micropore diffusion coefficients are found to be strongly concentration dependent. Adsorption isotherm slopes obtained from measured isotherms, the concentration-swing frequency response method, and a predictive method show reasonably good agreement.


ACS Applied Materials & Interfaces | 2018

Photocatalytic Oxidation of Sulfur Mustard and Its Simulant on BODIPY-Incorporated Polymer Coatings and Fabrics

Hui Wang; George W. Wagner; Annie Xi Lu; Dominique L. Nguyen; James H. Buchanan; Patrick M. McNutt; Christopher J. Karwacki

Sulfur mustard is one of the most toxic chemical warfare agents worldwide. We report the use of 4,4-difluoro-4-bora-3a,4a-diaza- s-indacene (BODIPY) photosensitizers as a fast and effective sulfur mustard decontaminant and their incorporation into various polymer coatings and fabrics, including army combat uniform. These BODIPY-embedded materials are capable of generating singlet oxygen under visible light irradiation and effectively detoxifying sulfur mustard by converting it into nontoxic sulfoxides as the major products. The rate of decontamination is found to be affected by the photosensitizer structure and concentration as well as the excitation wavelength. The most effective BODIPY-embedded self-decontamination material observed in this study shows a half-life of only 0.8 min. In comparison to the current methods, which use activated carbon as the adsorbent layer, these self-detoxifying coatings and fabrics provide constant destruction of and real-time protection against sulfur mustard.


Journal of Chemical & Engineering Data | 2009

Vapor Pressure of Organophosphorus Nerve Agent Simulant Compounds

Ann B. Butrow; James H. Buchanan; David E. Tevault


Langmuir | 1999

Effect of temperature on the desorption and decomposition of mustard from activated carbon

Christopher J. Karwacki; James H. Buchanan; John J. Mahle; Leonard C. Buettner; George W. Wagner


Journal of Materials Chemistry | 2016

Efficient and selective oxidation of sulfur mustard using singlet oxygen generated by a pyrene-based metal–organic framework

Yangyang Liu; Cassandra T. Buru; Ashlee J. Howarth; John J. Mahle; James H. Buchanan; Jared B. DeCoste; Joseph T. Hupp; Omar K. Farha


Langmuir | 1999

ADSORPTION EQUILIBRIA OF ISOPROPYL METHYLPHOSPHONOFLUORIDATE (GB) ON ACTIVATED CARBON AT ULTRALOW RELATIVE PRESSURES

Christopher J. Karwacki; David E. Tevault; John J. Mahle; James H. Buchanan; Leonard C. Buettner


International Journal of Thermophysics | 2006

Ambient Volatility of DMMP

D. E. Tevault; James H. Buchanan; Leonard C. Buettner


Journal of Chemical & Engineering Data | 2012

Thermophysical Properties of VX and RVX

David E. Tevault; Ann Brozena; James H. Buchanan; Patrice L Abercrombie-Thomas; Leonard C. Buettner


Journal of Chemical & Engineering Data | 2006

Vapor pressure of solid bis(2-chloroethyl) sulfide

James H. Buchanan; Leonard C. Buettner; David E. Tevault

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Leonard C. Buettner

Edgewood Chemical Biological Center

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John J. Mahle

Edgewood Chemical Biological Center

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Christopher J. Karwacki

Edgewood Chemical Biological Center

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George W. Wagner

Edgewood Chemical Biological Center

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Gregory W. Peterson

Edgewood Chemical Biological Center

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Jared B. DeCoste

Edgewood Chemical Biological Center

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