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M

ASTOVSKA

ET AL

.:

J

OURNAL OF

AOAC I

NTERNATIONAL

V

OL

.

98, N

O

. 2, 2015

483

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and fat, which are dependent on the silica deactivation. The

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2014.08A

for

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B. Apparatus

(

a

)

Homogenizer

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%/

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(

b

)

Solvent evaporator

.—Any suitable solvent evaporator,

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in both evaporation steps).

(

c

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Centrifuge

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(

d

)

Furnace/oven

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.

(

e

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Balance(s)

.—Analytical,

capable

of

accurately

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(

f

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Gas chromatograph-mass spectrometer

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requirements (to provide reliable results for the calibration

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2014.08A

).

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GC column

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other column that enables adequate separation of PAHs as

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see

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C. Reagents and Materials

(

a

)

Hexane.—

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(

b

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Isooctane.—

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(

c

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Ethyl acetate.—

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(

d

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Dichloromethane.—

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(

e

)

Toluene.—

•

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(

f

)

Water.—

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(

g

)

Anhydrous sodium sulfate (Na

2

SO

4

).—

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62

4

prepared and stored as indicated can be used for

1 month from preparation).

(

h

)

Silica gel SPE column.—

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naphthalene in the sample) are still acceptable if the source of

contamination could not be eliminated.

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2

62

4

.

(

i

)

Anhydrous magnesium sulfate (MgSO

4

).—

•

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prepared and stored as indicated

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Note

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can be used.

(

j

)

Sodium chloride (NaCl).—

•

(

k

)

Helium 5.0 or better, nitrogen 4.0 or better.

(

l

)

Polypropylene centrifuge tubes.—

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(

m

)

Glass Pasteur pipet.—

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(

n

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Syringes/pipets.—

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and transfer of appropriate volumes for standard solution

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(

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± P/

(

p

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Glassware for evaporation steps

.

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Table 2014.08B. (

continued

)

PAH

1R RI

laboratories

1R RI

replicates

Mean

concn, μg/kg

Mean

recovery, % s

r

, μg/kg s

R

, μg/kg RSD

r

, % RSD

R

, % HorRat

9

18

Naph

8

16

9

18

8

16

Phe

8

16

9

18

9

18

Pyr

9

18

9

18

8

16