Indiana University Bloomington
Department of Chemistry

Gary M. Hieftje

  • Distinguished Professor and Robert and Marjorie Mann Chair, Chemistry Department
  • Distinguished Professor, School of Public and Environmental Affairs

Education:

  • Ph.D. at University of Illinois at Urbana-Champaign, 1969
  • A.B. at Hope College, 1964

Contact Information:

(812) 855-2189
[send e-mail]
Room A150B

Background:

Research in our group generally involves the areas of spectrochemical analysis, chemical instrumentation, and information theory; with particular emphasis on mass spectrometry and optical techniques in the ultraviolet, visible, and infrared regions. Current projects include studies on basic atom formation, ionization, and excitation processes in flames and rare-gas plasmas, for use in atomic emission, absorption, mass, and fluorescence spectrometry; the development of new atomic methods of analysis; instrumental techniques to reduce the effects of background noise on measurements; computer-assisted chemical analysis; remote analysis based on fiber optics; near-infrared reflectance analysis; development of chromatographic detectors; plasma-source mass spectrometry; and picosecond time-resolved luminescence spectroscopy. Two of these projects are described briefly in the following paragraphs.

Flame and plasma atomic spectrometry are currently the most widely used techniques for elemental analysis. However, these methods are still impaired by interference among elements, limited sensitivity, and instrumental complexity. It is our firm belief that these limitations can be largely overcome by gaining a basic understanding of the underlying phenomena in each of the methods and then carefully designing improved instrumentation. To this end, we have a substantial ongoing effort to understand and mechanistically characterize the events leading to the formation, ionization, and excitation of atoms in flames and rare-gas plasmas. The efficiency with which atoms are formed, ionized, and excited governs both the sensitivity and the degree of elemental interference in such methods. Understanding the formation and excitation processes of atoms and ions will lead to a rational improvement in instrument performance.

In another area, novel mass spectrometers are being designed that are intended for use in the field of proteomics. A large fraction of known proteins contain metal atoms; in such situations, it is important to characterize not only the protein, but which metal atoms it contains, how many metal atoms there are, and if there is more than one kind of metal present. To address this problem, we have devised a novel time-of-flight mass spectrometer that accepts two ion sources simultaneously. When coupled to a separations device (LC or electrophoresis), this new tool is expected to be important in the characterization of proteins.


Selected Publications:

"Evolution and revolution in instrumentation for plasma-source mass spectrometry," with J. H. Barnes, et al. Pure Appl. Chem., 73, 1579 (2001).

Analytical capabilities of an inductively coupled plasma Mattauch-Herzog mass spectrometer," with D. A. Solyom, O. A. Grøn, and J. H. Barnes. Spectrochim. Acta, Part B, 56, 1717 (2001).

"Microwave plasma torch—atmospheric sampling glow discharge modulated tandem source for the sequential acquisition of molecular fragmentation and atomic mass spectra," with S. J. Ray. Anal. Chim. Acta, 445, 35 (2001).

"Standardless semiquantitative analysis of metals using single-shot laser ablation inductively coupled plasma time-of-flight mass spectrometry," with A. M. Leach. Anal. Chem., 73, 2959 (2001).

"Design and characterization of a radioluminescent temperature sensor," with A. M. Leach and R. A. Potyrailo. Anal. Chim. Acta, 412, 47 (2000).

"Use of the original silicone cladding of an optical fiber as a reagent-immobilization medium for intrinsic chemical sensors," with R. A. Potyrailo. Fres. J. Anal. Chem., 364, 32 (1999).

"Comparison of digital correlation techniques in time-resolved fluorometry using a radionuclide-scintillation excitation source," with D. L. Burden. Rev. Sci. Instru., 70, 50 (1999).

"Plasma-source sector mass spectrometry with array detection," with D. A. Solyom and T. W. Burgoyne. J. Anal. Atom. Spectrom., 14, 1101 (1999).

"Development of a direct current gas sampling glow discharge ionization source for the time-of-flight mass spectrometer," with J. P. Guzowski Jr., J. A. C. Broekaert, and S. J. Ray. J. Anal. Atom. Spectrom., 14, 1121 (1999).

"Preliminary investigations of electrothermal vaporization sample introduction for inductively coupled plasma time-of-flight mass spectrometry," with P. P. Mahoney, S. J. Ray, and G. Li. Anal. Chem., 71, 1378 (1999).

"Use of analyte-modulated modal power distribution in multimode optical fibers for simultaneous single-wavelength evanescent-wave refractometry and spectrometry," with R. A. Potyrailo and V. P. Ruddy. Anal. Chem., 71, 4956 (1999).

"Use of an air/argon microwave plasma torch for the detection of tetraethyllead," with B. W. Pack and Q. J. Jin. Anal. Chim. Acta, 383, 231 (1999).

"Characterization of 22-mm torch for ICP-AES," with J. A. Horner. Appl. Spectrosc., 53, 713 (1999).


Related News Stories

New technology may change the way common laboratory machine is made

Scientists at Indiana University and three other research centers have developed a more effective mass spectrometer, a device used by many scientists to find out what elements or compounds are in an unknown substance.   Full Story



Related Information:


Web Version:

http://Hieftje.chem.indiana.edu