Katherine S. Lovejoy
Los Alamos National Laboratory
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Publication
Featured researches published by Katherine S. Lovejoy.
Journal of Applied Phycology | 2013
Katherine S. Lovejoy; Lauren E. Davis; Lisa M. McClellan; Antonietta M. Lillo; John D. Welsh; Emily N. Schmidt; Claire K. Sanders; Alexander J. Lou; David T. Fox; Andrew T. Koppisch; Rico E. Del Sesto
Multiple ionic liquids (ILs) were assessed for their ability to extract branched, unsaturated hydrocarbons from an aqueous medium. In addition, IL cytotoxicity studies were performed on two phototrophic microbes, Synechocystis sp. PCC6803 and Botryococcus braunii var Showa. The optimum IL for use in an isoprenoid hydrocarbon extraction may vary based on the biological source of the isoprenoids. Our results suggest that ionic liquids have the potential to serve as novel biocompatible milking agents for extracting high-value chemicals from the microbes, with toxicity to both species minimized by considerations of ionic liquid structure and hydrophobicity.
Analytical Chemistry | 2011
Katherine S. Lovejoy; Geraldine M Purdy; Srinivas Iyer; Timothy Sanchez; Al Robertson; Andrew T. Koppisch; Rico E. Del Sesto
Room temperature ionic liquids, or RTILs, based on tetraalkylphosphonium (PR(4)(+)) cations were used as the basis of a platform that enables separation of dyes from textiles, extraction of dyes from aqueous solution, and identification of the dyes by MALDI-MS in a single experimental step for forensic purposes. Ionic liquids were formed with PR(4)(+) cations and ferulate (FA), α-cyano-4-hydroxycinnamate (CHCA), and 2,5-dihydroxybenzoate (DHB) anions. The use of tetraalkylphosphonium-based ionic liquids in MALDI-MS allowed detection of small molecule dyes without addition of a traditional solid MALDI matrix.
Analytical Chemistry | 2012
Katherine S. Lovejoy; Alexander J. Lou; Lauren E. Davis; Timothy Sanchez; Srinivas Iyer; Cynthia A. Corley; John S. Wilkes; Russell K. Feller; David T. Fox; Andrew T. Koppisch; Rico E. Del Sesto
Analytical capabilities to identify dyes associated with structurally robust wool fibers would critically assist crime-scene and explosion-scene forensics. Nondestructive separation of dyes from wool, removal of contaminants, and dye analysis by MALDI- or ESI-MS, were achieved in a single-pot, ionic liquid-based method. Ionic liquids (ILs) that readily denature the wool α-keratin structure have been identified and are conducive to small volume, high-throughput analysis for accelerated threat-response times. Wool dyed with commercial or natural, plant-based dyes have unique signatures that allow classification and matching of samples and identification of dyestuffs. Wool released 0.005 mg of dye per mg of dyed wool into the IL, allowing for analysis of single-thread sample sizes. The IL + dye mixture promotes sufficient ionization in MALDI-MS: addition of common MALDI matrices does not improve analysis of anionic wool dyes. An inexpensive, commercially available tetrabutylphosponium chloride IL was discovered to be capable of denaturing wool and was determined to be the most effective for this readily fieldable method.
Angewandte Chemie | 2003
Stefan Schiller; Renate Naumann; Katherine S. Lovejoy; Horst Kunz; Wolfgang Knoll
Crystal Growth & Design | 2012
Katherine S. Lovejoy; Cynthia A. Corley; Emily K. Cope; Michael C. Valentine; Jeff G. Leid; Geraldine M Purdy; John S. Wilkes; Andrew T. Koppisch; Rico E. Del Sesto
Photochemical and Photobiological Sciences | 2006
Frederick D. Lewis; Paul C. Karagiannis; Meledathu C. Sajimon; Katherine S. Lovejoy; Xiaobing Zuo; Michael Rubin; Vladimir Gevorgyan
Archive | 2013
Katherine S. Lovejoy; Rico E. Del Sesto; Andrew T. Koppisch
Chemical Communications | 2017
Todd C. Monson; Tyler E. Stevens; Jean L. Leger; Jamie L. Manson; Katherine S. Lovejoy; Aimee L. Newsham; Rico E. Del Sesto
Archive | 2014
Rico E. Del Sesto; Andrew T. Koppisch; Katherine S. Lovejoy; Geraldine M Purdy
Archive | 2013
Katherine S. Lovejoy; Rico E. Del Sesto; Andrew T. Koppisch