Effect of Experimental Parameters on the ESI FT-ICR Mass Spectrum of Fulvic Acid

Teresa L. Brown and James A. Rice*
Department of Chemistry and Biochemistry, South Dakota State University, Brookings, South Dakota 57007-0896
Anal. Chem., 2000, 72 (2), pp 384–390
DOI: 10.1021/ac9902087
Publication Date (Web): December 8, 1999
Copyright © 2000 American Chemical Society
*

 Corresponding author. Phone:  (605) 688-4252. Fax:  (605) 688-6364. E-mail:  James_Rice@sdstate.edu.

Abstract

Fulvic acid (FA) is a heterogeneous mixture of organic macromolecules found in the waters, soils, and sediments of the earth's surface. The ability of electrospray ionization (ESI) to effectively transfer large ions from the solution phase to the gas phase and the coupling of ESI to the high-mass-resolution capabilities of Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) provide a potential method for the mass spectrometric analysis of FA. Positive- and negative-ion ESI FT-ICR MS analyses of four reference International Humic Substances Society FAs were performed. The spray solution composition was found to have a dramatic effect on the ion distributions, with high-mass aggregates (m/z 2000−4000) being formed in less polar spray solutions. Positive-ion spectra for each FA obtained under optimum conditions resulted in number-average molecular weights ranging from 1700 to 1900. The mass spectra were extremely complex, with ion distributions on the order of m/z 500−3000. The presence of more than one ion at each nominal mass was routinely observed. Negative-ion ESI analysis of the FA samples resulted in the observation of multiply charged ions whose distributions could be affected by the acidification of the spray solution. Solution parameters which have been reported to affect molecular weight distributions of FA such as pH, ionic strength, and concentration of multivalent cations were found to have little or no effect on the observed m/z distributions.

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History

  • Published In Issue January 15, 2000
  • Received for review February 23, 1999. Accepted October 22, 1999.

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