Atmospheric pressure photoionization mass spectrometry as a tool for the investigation of the hydrolysis reaction mechanisms of phosphite antioxidants


Autoria(s): PAPANASTASIOU, M.; MCMAHON, A. W.; ALLEN, N. S.; JOHNSON, B. W.; KECK-ANTOINE, K.; SANTOS, L.; NEUMANN, M. G.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2008

Resumo

The hydrolysis reaction mechanism of phosphite antioxidants is investigated by liquid chromatography-mass spectrometry (LC/MS). The phosphites were chosen because they differed in chemical structure and phosphorus content. Dopant assisted-atmospheric pressure photoionization (DA-APPI) is chosen as the ion source for (lie ionization of the compounds. [it our previous work, DA-APPI was shown to offer an attractive alternative to atmospheric pressure chemical ionization (APCI) since it provided background-ion free mass spectra and higher sensitivity [M. Papanastasiou, et al., Polymer Degradation and Stability 91 (11) (2006) 2675-2682]. In positive ion mode, the molecules are generally detected in their protonated form. In negative ion mode, the phosphites are unstable and only fragment ions are observed: these however, are characteristic of each phosphite and may be used for the identification of the analytes in complex mixtures. The analytes under investigation are exposed to accelerated humid ageing conditions and their hydrolytic pathway and stability is investigated. Different substituents around the phosphorus atom are shown to have a significant effect on the stability of the phosphites, with phenol substituents producing very hydrolytically stable structures. Alkanox P24 and PEP-36 follow a similar hydrolytic pathway via the scission of the first and then the second P-O-phenol bonds, eventually leading to the formation of phenol, Phosphorous acid and pentaerythritol as end products. HP-10 exhibits a rather different Structure and the products detected suggest scission of either the P-O-hydrocarbon or one of the P-O-phenol bonds. A phenomenon similar to that of autocatalysis is observed for all phosphites and is attributed to the formation of dialkyl phosphites as intermediate products. (C) 2008 Elsevier B.V. All rights reserved.

Applied Biosystems/MDS Sciex

Applied Biosystems/MDS Sciex

GlaxoSmithKline

GlaxoSmithKline

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fapesp[04/02112]

Capes[4491-05-0]

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Identificador

INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, v.275, n.1/Mar, p.45-54, 2008

1387-3806

http://producao.usp.br/handle/BDPI/31564

10.1016/j.ijms.2008.05.012

http://dx.doi.org/10.1016/j.ijms.2008.05.012

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE BV

Relação

International Journal of Mass Spectrometry

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE BV

Palavras-Chave #dopant assisted-atmospheric pressure photoionization #mass spectrometry #phosphite antioxidants #hydrolysis #LIQUID-CHROMATOGRAPHY #POLYMER STABILIZERS #FLAME RETARDANTS #POLYPROPYLENE #IONIZATION #PERFORMANCE #ADDITIVES #ACETONITRILE #DIPHOSPHITE #EXTRACTION #Physics, Atomic, Molecular & Chemical #Spectroscopy
Tipo

article

original article

publishedVersion