Laser desorption ionization and MALDI time-of-flight mass spectrometry for low molecular mass polyethylene analysis

被引:53
|
作者
Chen, R
Yalcin, T
Wallace, WE
Guttman, CM
Li, L
机构
[1] Univ Alberta, Dept Chem, Edmonton, AB T6G 2G2, Canada
[2] NIST, Div Polymers, Gaithersburg, MD 20899 USA
[3] Univ Alberta, Dept Chem, Edmonton, AB, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
D O I
10.1016/S1044-0305(01)00308-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Polyethylene's inert nature and difficulty to dissolve in conventional solvents at room temperature present special problems for sample preparation and ionization in mass spectrometric analysis. We present a study of ionization behavior of several polyethylene samples with molecular masses up to 4000 Da in laser desorption ionization (LDI) time-of-flight mass spectrometers equipped with a 337 nm laser beam. We demonstrate unequivocally that silver or copper ion attachment to saturated polyethylene can occur in the gas phase during the UV LDI process. In LDI spectra of polyethylene with molecular masses above similar to 1000 Da, low mass ions corresponding to metal-alkene structures are observed in addition to the principal distribution. By interrogating a well-characterized polyethylene sample and a long chain alkane, C94H190, these low mass ions are determined to be the fragmentation products of the intact metal-polyethylene adduct ions. It is further illustrated that fragmentation can be reduced by adding matrix molecules to the sample preparation. (C) 2001 American Society for Mass Spectrometry.
引用
收藏
页码:1186 / 1192
页数:7
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