Pergamon
0043-1354(93)E0023-L
War. Res. Vol. 28, No. 7, pp. 1595-1600, 1994
Copyright © 1994 Elsevier Science Ltd
Printed in Great Britain. All rights reserved
0043-1354/94 $7.00 + 0.00
TASTE AND ODOUR DEVELOPMENT IN WATER IN
POLYETHYLENE CONTAINERS EXPOSED TO DIRECT
SUNLIGHT
LUCIA CALVOSA 1, GERMANA CHIODINI 2, WALTERCORETTI 3, PAOLODONAGGIO 1,
MARCO ORLANDI 2, VALERIOPARATICI 2 and BRUNORINDONE2*O
~Enichem, via Iannozzi 1, 1-20097 San Donato Milanese, Italy, 2Dipartimento di Chimica Organica e
Industriale, Universita' di Milano, via Venezian 21, 1-20133 Milano, Italy and 3Water Line S.A., CH
6805-Mezzovico, Lugano, Switzerland
(First received March 1992; accepted in revised form November 1993)
Abstract--Drinking water samples contained in Low Density Polyethylene(LDPE) and exposed to direct
sunlight for 2 weeks were analysed to identify substances responsible for taste and odour development.
Identical samples not exposed to direct sunlight and samples contained in glass bottles were used as
reference material.
The analyses were performed by passing water through a column of purified Amberlite XAD-2 resin
Coolystyrene-divinylbenzene), to concentrate trace compounds. Solvent eluates from the resin were
concentrated 50 times and analysed by gas chromatography and gas chromatography-mass spectrometry.
Butyl vinyl ketone, deriving from the photodecomposition of LDPE, together with benzophenone,
3.5-dimethoxybenzaldehyde, n-butylphthalate and i-butylphthalate, deriving from the ink, were found in
water exposed to direct sunlight.
The addition of horseradish peroxidase to water stored in PE containers resulted in lower taste and
odour development.
Key words---drinking water, taste and odour, irradiation, solid phase extraction, GC-MS, GC-FTIR,
horseradish peroxidase
INTRODUCTION
The increasing use of plastic films for the packaging
of food and drink calls for more information con-
cerning the interactions of such plastic packaging
materials with food and drinks (Halek et al., 1988).
During droughts it is a common practice to use
transportable plants to make local water potable and
to store it in LDPE bags. However, taste and odours
are known to develop in these containers, especially
after direct exposure to sunlight for long periods. The
primary reasons for these organoleptic changes have
been suggested (Flogstad, 1984):
(a) photooxidation of polyethylene (PE) and the
dissolution of the resulting compounds;
(b) photooxidation of secondary PE components,
such as residual solvents or ethylene oligomers;
(c) photooxidation of external inks and migration
of products through PE;
(d) migration of external contaminants through
PE.
In fact, it is often the transfer of material from or
through the packaging that is the origin of off-flavors
in food (Flogstad, 1984). Furthermore, plastic pack-
*Author to whom all correspondence should be addressed.
ing film is often printed with inks that release residual
solvents such as hydrocarbons, alcohols, ketones and
esters (Mehens et al., 1984) into the plastic. These
compounds then migrate to the packaged food (Kim
and Gilbert, 1989) and contribute sensory defects
because of their low flavor thresholds (Halek et al.,
1988).
This study reports on the concentration and
identification of compounds released into drinking
water samples from polymeric packaging, and print-
ing ink.
EXPERIMENTALSECTION
Local well water was used for this work unless otherwise
stated. Polyethylene (PE) was an Enichem product. HPLC-
grade water was a Merck product. Horseradish peroxidase
was a Sigma product. Samples were stored in a well aerated
dark room and were analysed after 15 days. The exposition
to direct sunlight occurred putting the samples on the roof
of the building for 15 days in June.
Extraction method
The use of XAD macroreticular resins for the recovery of
low concentrations of organic pollutants from water is well
documented (Halek and Levinson, 1989). In this study
XAD-2 resin (polystyrene~divinylbenzene) was used to ex-
tract organic compounds from drinking water. The organics
were then eluted with diethyl ether and the eluate was
concentrated by evaporation. The organic components were
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