Skip to main content
U.S. flag

An official website of the United States government

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry of Covalently-Cationized Polyethylene as a Function of Sample Temperature

Published

Author(s)

William E. Wallace, William R. Blair

Abstract

A pre charged, low mass, low polydispersity linear polyethylene was analyzed with matrix assisted laser desorption/ionization (MALDI) mass spectrometry as a function of sample temperature between 25 C and 150 C. This temperature range crosses the polyethylene melting temperature. Buckminsterfullerene (C60) was used as MALDI matrix due to the high volatility of typical MALDI matrices making them unsuitable for heating in vacuum. Starting at 90 C there is an increase in ion intensity at fixed laser energy. By 150 C the integrated total ion intensity had grown by six fold indicating that melting did indeed increase ion yield. At 150 C the threshold laser intensity to produce intact polyethylene ions decreased by about 25%. Nevertheless, significant fragmentation accompanied the intact polyethylene ions even at the highest temperatures and the lowest laser energies.
Citation
International Journal of Mass Spectrometry
Volume
263

Keywords

mass spectrometry, matrix-assisted laser desorption ionizat, polyethylene

Citation

Wallace, W. and Blair, W. (2007), Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry of Covalently-Cationized Polyethylene as a Function of Sample Temperature, International Journal of Mass Spectrometry, [online], https://tsapps.nist.gov/publication/get_pdf.cfm?pub_id=852704 (Accessed December 4, 2024)

Issues

If you have any questions about this publication or are having problems accessing it, please contact reflib@nist.gov.

Created January 1, 2007, Updated February 19, 2017