JTSR-2015v5n9 - page 8

Journal of Tea Science Research. 2015, Vol. 5, No. 9, 1-7
6
4.4.2 Clean up
The extract was evaporated to dryness on a rotary
vacuum evaporator and the residue was dissolved in
10 ml hexane and again transferred to 125 ml
separating funnel. The round bottom flask was
rinsed with 5 ml portions of hexane and the rinses
were added to the separating funnel. About 30 ml
acetonitrile–saturated with hexane was added to it
and the acetonitrile layer was drained into a 250 ml
round bottom flask containing anhydrous sodium
sulphate. The acetonitrile extract was evaporated to
dryness at 60°C. The concentrated residue was
dissolved in 5 ml hexane and cleaned up by
adsorption column chromatography using
10 g of 5% deactivated florisil and 150 ml of 6%
diethyl ether in hexane as eluting solvent. Prior
to elution, the column was washed with 50 ml of
hexane to remove the co-extractives. The collected
elution was concentrated at about 60°C to dryness
and dissolved with 10 ml of hexane and injected into
GLC as per the standard operating conditions
(AOAC, 2005).
4.4.3 Preparation of acetonitrile saturated with
hexane
Three portions of acetonitrile were combined
with one portion of hexane in a 125 ml separating
funnel, gently shaken and then the lower part of
acetonitrile layer was collected. This is called
acetonitrile saturated with hexane.
4.4.4 Bifenthrin residues in tea brew
2 g of made tea was infused in 100 ml of boiling
water (ISO 3103 -1990). After 6 minutes of brewing,
the water extract was filtered, cooled and partitioned
with 100 ml of hexane. The organic phase was
passed through anhydrous sodium sulfate. The
extract was concentrated by evaporating in a rotary
vacuum evaporator and dissolved with 10 ml hexane
and analysed for the residues of bifenthrin. The
spent leaves were dried between the folds of
filter paper and residues were extracted following
the method described above for black tea.
Authors Contributions
SS conducted the field trials, sample preparation,
residue analysis and interpreted the results. NM
approved the protocol and drafted the manuscript.
Acknowledgements
The authors are grateful to the National Tea
Research Foundation (NTRF), C/o. Tea Board, Govt.
of India for the financial assistance for this work.
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