TY - JOUR
T1 - Pyrolysis study of halogen-containing aromatics reflecting reactions with polypropylene in a posttreatment decontamination process
AU - Balabanovich, Aliaksandr I.
AU - Hornung, Andreas
AU - Luda, Maria P.
AU - Koch, Wolfgang
AU - Tumiatti, Vander
N1 - MEDLINE® is the source for the MeSH terms of this document.
PY - 2005/7/15
Y1 - 2005/7/15
N2 - Halogen-containing aromatics, mainly bromine-containing phenols, are harmful compounds contaminating pyrolysis oil from electronic boards containing halogenated flame retardants. In addition, theirformation increases the potential for evolution of polybrominated dibenzo-p-dioxins (PBDDs) and dibenzofurans (PBDFs) at relatively low temperature (up to 500 °C). As a model compound, 2,4-dibromophenol (DBP) was pyrolyzed at 290-450 °C. While its pyrolysis in a nitrogen flow reactor or in encapsulated ampules yields bromine-containing phenols, phenoxyphenols, PBDDs, and PBDFs, pyrolysis of DBP in a hydrogen-donating medium of polypropylene (PP) at 290-350 °C mainly results in the formation of phenol and HBr, indicating the occurrence of a facile hydrodebromination of DBP. The hydrodebromination efficiency depends on temperature, pressure, and the ratio of the initial components. This thermal behavior of DBP is compared to that of 2,4-dichlorophenol and decabromodiphenyl ether. A treatment of halogen-containing aromatics with PP offers a new perspective on the development of low-environmental-impact disposal processes for electronic scrap.
AB - Halogen-containing aromatics, mainly bromine-containing phenols, are harmful compounds contaminating pyrolysis oil from electronic boards containing halogenated flame retardants. In addition, theirformation increases the potential for evolution of polybrominated dibenzo-p-dioxins (PBDDs) and dibenzofurans (PBDFs) at relatively low temperature (up to 500 °C). As a model compound, 2,4-dibromophenol (DBP) was pyrolyzed at 290-450 °C. While its pyrolysis in a nitrogen flow reactor or in encapsulated ampules yields bromine-containing phenols, phenoxyphenols, PBDDs, and PBDFs, pyrolysis of DBP in a hydrogen-donating medium of polypropylene (PP) at 290-350 °C mainly results in the formation of phenol and HBr, indicating the occurrence of a facile hydrodebromination of DBP. The hydrodebromination efficiency depends on temperature, pressure, and the ratio of the initial components. This thermal behavior of DBP is compared to that of 2,4-dichlorophenol and decabromodiphenyl ether. A treatment of halogen-containing aromatics with PP offers a new perspective on the development of low-environmental-impact disposal processes for electronic scrap.
KW - bromine
KW - environmental impact
KW - halogen compounds
KW - phenols
KW - atomatic hydrocarbons
UR - http://www.scopus.com/inward/record.url?scp=22344453955&partnerID=8YFLogxK
UR - http://pubs.acs.org/doi/abs/10.1021/es0500106
U2 - 10.1021/es0500106
DO - 10.1021/es0500106
M3 - Article
AN - SCOPUS:22344453955
SN - 0013-936X
VL - 39
SP - 5469
EP - 5474
JO - Environmental Science and Technology
JF - Environmental Science and Technology
IS - 14
ER -