H. Kylin et al., DETERMINATION OF CHLORINATED PESTICIDES AND PCB IN PINE NEEDLES - IMPROVED METHOD FOR THE MONITORING OF AIRBORNE ORGANOCHLORINE POLLUTANTS, Fresenius' journal of analytical chemistry, 356(1), 1996, pp. 62-69
A method to determine organochlorine pollutants in pine needles is des
cribed. Fresh, whole needles have been extracted for 48 h in dichlorom
ethane to obtain the epicuticular wax fraction. The remainder has been
cut into small pieces and again extracted with dichloromethane to obt
ain the internal lipids. Prior to gas chromatography, both the wax and
the internal lipid extracts have been fractionated on two columns: fi
rst a silica gel/silica gel:sulphuric acid 2:1 column with dichloromet
hane as eluent and then a nitrophenyl silica column with hexane as elu
ent. Three fractions have been collected, fraction 1 containing hexach
lorobenzene (HCB), fraction 2 containing polychlorinated biphenyls (PC
B) and 1,1-dichloro-2,2-bis(4-chlorophenyl)ethene (DDE), and fraction
3 containing the remaining, more polar, organochlorine pesticides. For
some pine species, the nitrophenyl silica column has been combined wi
th a short aminopropyl silica column to obtain chromatograms of the PC
B fraction free from negative peaks. The precision is in the range of
4-12% relative standard deviation, and the overall recovery is around
65-90%.