Chemosphere, Vol.13, No.4, P r i n t e d in Great B r i t a i n
pp 521 - 525,
1984
0 0 4 5 - 6 5 3 5 / 8 4 $3.00 + .00 ©1984 P e r g a m o n Press Ltd.
S P E C I F I C I T Y OF A N A L Y T I C A L M E T H O D S USED TO D E T E R M I N E THE C O N C E N T R A T I O N OF F O R M A L D E H Y D E IN W O R K R O O M A I R Ilpo Ahonen*, Tampere
Eero Priha
and M a r j a - L i i s a
Aij~l~
Regional Institute of O c c u p a t i o n a l Health Box 486, SF-33101 T a m p e r e i0 F i n l a n d
ABSTRACT
I n t e r f e r e n c e s from 17 c o m m o n l y occurring o r g a n i c c o m p o u n d s to the d e t e r m i n a t i o n of f o r m a l d e h y d e have b e e n studied. The tested m e t h o d s were a c e t y l a c e t o n e ( c o l o r i m e t r i c and fluorometric) c h r o m o t r o p i c acid (with and w i t h o u t evaporation), MBTH, p a r a r o s a n i l i n e and 2 , 4 - d i n i t r o p h e n y l h y d r a t z i n e - H P L C methods.
INTRODUCTION
Several
analytical
formaldehyde published serious
methods
in w o r k r o o m
m a n y other
respect
used
air p o l l u t a n t s
Specificity
is p e r h a p s
chromotropic
occur
with
retained
according
to an a c e t y l a c e t o n e
may
interferences
•
cause
be more
specific
knowledge method
about
the
sample level
actual
method
specific
with
methods
ketones
can
sampling
9 .
other
The
no other
or p o t e n t i a l
interfere
methods.
from m a n y
to dryness
of f o r m a l d e h y d e
aldehydes,
amines,
is one way is d e t e r m i n e d
and k e t o c o m p o u n d s
p r o c e d u r e 5 has been but there
of total
limited
claimed
hydrazone
aliphatic
(MBTH)
a l d e h y d e s 6. When
can be used
information
to
is no systematic
about
to d e t e r m i n e the effects
i n t e r f e r e n c e s I'7. A 2,4-dinitrophenylhydroazine
f o r m a l d e h y d e 8'9. with
in w h i c h
a l d e h y d e s I, phenol I, ethanol 2,
the M B T H m e t h o d
is only
air,
to suffer
3-methyl-2-benzothiazolone
HPLC or GC a n a l y s i s
for
reported
acid method,
aldehydes,
There
is e s p e c i a l l y
in w o r k r o o m
solution
level
for d e t e r m i n a t i o n s
of f o r m a l d e h y d e .
of n u m e r o u s
method,
the c h r o m o t r o p i c
used
contains
the
. The p a r a r o s a n i l i n e
interferences.
is c o m m o n l y
the
(DNPH)
than
4
When
of
study has been
lack
the s p e c t r o p h o t o m e t r i c
has been
such as a l c o h o l s I, other
interferences.
concentration
formaldehyde.
problem with
and x y l e n e s 2. E v a p o r a t i o n 3 of the a b s o r p t i o n to expel
This
of f o r m a l d e h y d e
acid p r o c e d u r e
the
no systematic
compounds.
together
the g r e a t e s t
interferences
to d e t e r m i n e
but v i r t u a l l y
from o r g a n i c
to m e a s u r e m e n t s
The c l a s s i c negative
air,
on i n t e r f e r e n c e s
with
have been
the m e t h o d
is c o m m o n l y Only
large
if 2 , 4 - D N P H
521
considered
amounts coated
one of the most
of other XAD-2
aldehydes
resin
is used
or for
522
This paper
discusses
formaldehyde. occur
Most
together
clinical
the
specificity
of the
with
studied
formaldehyde
laboratories,
and
studied
acetylacetone
TABLE
i.
and
Methods
are
five
potential
commonly
used methods
interferences
in t h e w o o d w o r k i n g
were
to determine
solvents,
industry,
which
foundries,
elsewhere.
RESULTS
The methods
of
shown
chromotropic
AND DISCUSSION
in t a b l e acid
i. T w o d i f f e r e n t
methods
were
modifications
of the
tested.
studied
Method
Absorption
Wavelength
solution
nm
Reference
or adsorbent
acetylacetone
i0 % m e t h a n o l
- colorimetric
(AAcolor.)
- fluorometric
(AAfluor.)
chromotropic - without (CTA - with (CTA
4,
in w a t e r
i0
415 410ex/510em
acid
1%
evaporation
sodium
580
ii
340
9,
610
13
570
5
bisulfite
)
no evap. evaporation evap.
)
2,4-dinitrophenylhydrazine-
XAD-2
HPLC
with
2,4-DNPH
0.05
% MBTH
(DNPH)
3-methyl-2-benzothiazolone hydrazone
coated
12
(MBTH)
pararosaniline
(PRA)
distilled water
As
can be
seen
from table
the d e t e r m i n a t i o n deviation
of
2,
several
formaldehyde.
of each method
are here
o f the
compounds
Only differences considered
studied
over
as a c t u a l
twice
interfered the
with
standard
interferences.
523
TABLE
2.
Effects
of
the
compounds
tested
on
the
results
of
formaldehyde
Relative
result I
(i p p m
HCHO
= i00)
Mole AA
ratio
CTA
DNPH
color
Compound
MBTH
PRA
fluor
no evap.
evap.
i00
i01
96*
102
i00
100
i00
n-propanol
99
98
96*
103
i00
i00
i00
i-propanol
ethanol
i00:i
i00
99
85*
102
i00
i01
99
n-butanol
99
I00
88*
103
i00
i00
i00
i-butanol
99
i00
67*
i01
i00
i01
i00
methyl
i-butylketone
i00
96
95*
109"
I00
103"
i01
113"
115"
117"
129"
114"
152"
119"
"
I00
98
98
106"
92
i01
i00
"
i01
98
92*
106"
92
103"
i01
"
99
103
26*
102
i00
I00
"
99
98
70*
104"
92
113"
i01
"
i00
99
35*
107"
92
112"
103"
i01
2-ethoxyethanol (cellosolve) ethyl
acetate
n-butyl
acetate
xylene white
spirit
aromatic
white
(Shellosol furfuryl
spirit
i00
A) 5:1
i01
93*
acetaldehyde
"
i01
95
acrolein
"
i01
102
"
i00
99
96*
104"
102
i00
i00
"
i00
i00
17"
109"
102
i00
99
formic
alcohol
acid
phenol
*
interference
i)
each
The
compounds
excess. pling and
is
way
procedure A)
Therefore
concluded
2 x relative the
tested
In t h i s
Shellsol
utions. be
>+
result
on
mean
were the
not
the the
standard three
injected
maximum
especially are
of
actual
basis
of
into
table
158"
103
>>150"
120"
98
103
102
>>150"
112"
of
absorption was
compounds
2.
102
104"
in
the
method
determinations
solutions obtained.
(such
quantitatively
interference
134"
88*
deviation
duplicate
interference
nonpolar
absorbed
i00
into
such
as
at
xylene,
aqueous
case
a certain
In n o r m a l white
air
spirit,
absorption
is m u c h
lower
molar sam-
sol-
than
can
524
It is o b v i o u s aldehyde results
Mole
compound
since
(Riedel
it c a u s e d
de H a e n
a positive
corresponding
that
to interference
an e r r o r
the
over
of
i0 % ( t a b l e
interference
3.
Interpolated
Compound
is
i0 % w e r e 3).
linearly
mole
ratios
Mole
(about
some
15 %)
The
calculated
calculation
correlated
that
ratio
caused
with
formin the
for e a c h
is b a s e d
the
i-propanol
67
n-butanol
83
i-butanol
30
xylene
14
white
spirit
aromatic
white
(Shellsoll furfuryl
spirit
33
77
15
83
A) 1,6
0,9
4,2
4,2
<
acrolein
2,5
<
phenol
0,6
acetylacetone
methods
(both colorimetric
2,4-dinitrophenylhydrazine Except
PRA
evap.
alcohol
acetaldehyde
studied.
HCHO)
MBTH
for
method
were
2-ethoxyethanol,
i0 % i n t e r f e r e n c e
with
these
and
the most
none
of the
fluorometric) specific
and
the
of the methods
compounds
tested
caused
two methods.
EXPERIMENTAL
Reagents:
All
or a n a l y t i c a l made
according
the
reagents
grade.
The
were
commercially
chemosorbent
to Andersson
et al 9.
tubes
available for t h e
pro-analytical
2,4-DNPH
on
concentration
i0 % i n t e r f e r e n c e
(interferent:
CTA n o evap.
over
contains
error
compound.
TABLE
The
24206)
the methods.
that had
assumption
2-ethoxyethanol
impurity,
o f all
ratios
of t h e
that
as a n
method
were
525
Instruments:
The c o l o r i m e t r i c
spectrophotometer fluorometer
determinations (water
syringe
were
formaldehyde) diluted
Three
sample,
were
duplicate
performed
been
determinations
according
to the
5000 HPLC with
was
to w h i c h
(corresponding
spectro-
measurements. a isocratic
HPLC
eluation
injected a known
by m i c r o l i t e r
concentration
to 1 p p m HCHO in the air
The mole
Some c o m p o u n d s
Bowman
1800
4020 UV-detector.
compounds
3 liter).
with
An A m i n c o
fluorometric
solutions
added
or 5:1.
(acrolein
done b y a Pye U n i c a m
a Pye U n i c a m
of o r g a n i c
DNPH w i t h
I00:i
with water
Model
with
amount
for the
or d e s o r p t i o n
had a l r e a d y
a 15 liter
used
done by a V a r i a n
A certain
were
a i0 m m autocell.
70) e q u i p p e d
into a b s o r p t i o n
formaldehyde
with
with
i0 m m cells was
30/methanol
Test p r o c e d u r e :
of
equipped
with
measurements
ratios
(test compound:
(added in ratio
5:1)
were
first
ethanol).
were made
instructions
in each
case.
specified
The a n a l y t i c a l
in the r e f e r e n c e s
stage was (Table
I).
REFERENCES
i. J. Skare,
B. Dahlner,
2. C. W. Lee, 3. C.E.
Y.S.
Bricker,
4. P. Bisgaard, dehyddampe
Arbete
Fung,
W.V.
och H~isa,
1973:6.
K.W.
Fung,
Analyst
Aubrey,
Anal.
Chem.
L. M~lhave,
i arbejds-
B. Rictz,
(In Swedish)
107:30
22:720
(1982).
(1950).
P. Wildharclt,
og opholdsrum,
M~ling
af formal-
Arbejdsmilj~fondet,
Copenhagen
1982.
(In Danish). 5. R.R.
Miksch,
D.W.
J. Glanville, 6. R.R. 7. E.
Miksch,
Sawicki,
Academic 8. C.A.
Anal. D.W.
C.R.
press,
Nilsson,
i0. L i n s t e d t
Chem.
Sawicki, London
et al,
Unders~kningsrapport ii.
Standard
SFS 3862
12. V a r i a n 13. A P H A ed,
Intersociety
(Received
K. Revzan,
Hyg.
Assoc.
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(1982).
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Vol.
i.,
1975. Chemosphere J.O.
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Levin,
C.A.
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Scand.
J. Work
(1981). Best~mning 1981:16.
(Ty6paikan
av f o r m a l d e h y d
i hudreng6rningsmedel.
Arbetarskyddsstyrelsen ilman
1981.
formaldehydipitoisuuden
Finnish
Standardisation
(In Swedish). m~ritys
Association.
1978.
Instruments
APHA
Hollowell,
(1981).
Ind.
kromotrooppihappomenetelm~ll~). Helsinki
G.D.
Aldehydes-Photometric
Levin,
7:282
Fanning,
53:2118 Am.
C. Hallgren,
Health G.,
L.Z.
Anthon,
J-O.
9. K. Andersson, Environ.
Anthon,
at Work, Commitee,
Interdisplinary
in The N e t h e r l a n d s
Number
LC 132.
Methods
Books
for Air
Varian
Sampling
& Periodicals,
14 F e b r u a r y
1984;
Associates
and A n a l y s i s
Washington
accepted
Inc.
1977,
20 F e b r u a r y
1981. 2 nd
308. 1984)