Quantitative analysis of an oligomeric hindered amine light stabilizer in polypropylene by matrix-assisted laser desorption/ionization mass spectrometry using a solid sampling technique

被引:10
作者
Taguchi, Y
Ishida, Y
Matsubara, H
Ohtani, H [1 ]
机构
[1] Nagoya Inst Technol, Dept Mat Sci & Engn, Grad Sch Engn, Nagoya, Aichi 4668555, Japan
[2] Toray Res Ctr Ltd, Organ Anal Labs, Otsu, Shiga 5208567, Japan
[3] Nagoya Univ, Eco Topia Sci Inst, Nagoya, Aichi 4648603, Japan
[4] Aichi Ind Technol Inst, Kariya, Aichi 4480003, Japan
关键词
D O I
10.1002/rcm.2452
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A small amount of an oligomeric hindered amine light stabilizer (HALS) (Adekastab LA-68LD) in polypropylene (PP) materials was directly determined by solid sampling matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) using an internal standard method. First the matrix reagent (dithranol), 20 mg, and the empirically selected internal standard, angiotensin I (MW = 1296.5), 5 mu g, were premixed in the solid state. The matrix mixture was then co-ground with the PP sample containing the HALS in liquid nitrogen using a freezer mill. The powdered sample mixture was spotted on the sample plate, suspended in ion-exchanged water, dried to adhere on the plate, and subjected to MALDI-MS. Three series of the HALS components accompanied by the oxidized species were clearly observed as their molecular ions (M.+) along with that of the internal standard in the mass spectra. A fairly good linear relationship (R-2 = 0.9991) with a relative standard deviation of ca. 11% was observed between the relative peak intensities of the HALS components and the HALS contents ranging from 0.1-2.5 wt%, which could be used as the calibration line to determine the HALS content in PP composites directly by MALDI-MS. The UV-exposed PP composite samples were evaluated by this method to interpret the photostabilizing action of HALS in the PP materials based on the observed change in the relative abundances of the original and oxidized HALS components as a function of UV-exposure time. Copyright (c) 2006 John Wiley & Sons, Ltd.
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页码:1345 / 1350
页数:6
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