Abstract:
:Oxidative coupling reactions take place during the passage of xylenols through a laboratory-scale helophyte-based constructed wetland system. Typical coupling product groups including tetramethyl-[1,1'-biphenyl] diols and tetramethyl diphenylether monools as stable organic intermediates could be identified by a combination of pre-chromatographic derivatization and GC/MS analysis. Structural assignment of individual analytes was performed by an increment system developed by Zenkevich to pre-calculate retention sequences. The most abundant analyte turned out to be 3,3',5,5'-tetramethyl-[1,1'-biphenyl]-4,4'-diol, which can be formed by a combination of radicals based on 2,6-xylenol or by an attack of a 2,6-xylenol-based radical on 2,6-xylenol. Organic intermediates originating from oxidative coupling could also be identified in anaerobic constructed wetland systems. This finding suggested the presence of (at least partly) oxic conditions in the rhizosphere.
journal_name
Chemospherejournal_title
Chemosphereauthors
Poerschmann J,Schultze-Nobre L,Ebert RU,Górecki Tdoi
10.1016/j.chemosphere.2014.06.004subject
Has Abstractpub_date
2015-01-01 00:00:00pages
184-189eissn
0045-6535issn
1879-1298pii
S0045-6535(14)00736-Xjournal_volume
119pub_type
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