INTERNATIONAL
STANDARD 749
INTERNATIONAL ORGANIZATION FOR STANDARDIZATION l
FOREWORD
IS0 (the International Organization for Standardization) is a worldwide federation
of national standards institutes (IS0 member bodies). The work of developing
International Standards is carried out through IS0 technical committees. Every
member body interested in a subject for which a technical committee has been set
up has the right to be represented on that committee. International organizations,
governmental and non-governmental, in liaison with ISO, also take part in the work.
) EW
b-
Draft International Standards adopted by the technical committees are circulated
ea
.ai VI
to the member bodies for approval before their acceptance as International
77 2a
teh RE
Standards by the IS0 Council.
19 a
9- / 9d
s.i P
74 st
o- /si
rd D
International Standard IS0 749 was developed by Technical Committee
/ i s ds
da AR
ISO/TC 34, Agricultural food products.
d0 a r
99 /st :
a d
22 og r d
an D
0a an
a
(st AN
7 2 ta l d
It was submitted directly to the IS0 Council, in accordance with clause 6.12.1 of
-b c a a n
ST
the Directives for the technical work of ISO. It cancels and replaces IS0
dc ai/ l st
9 b h. ul
Recommendation R 749-1968, which had been approved by the member bodies of
eh
1 - i te F
the following countries :
iT
5d s.
Australia India Romania
-4 r d
Brazil Iran South Africa, Rep. of
e c da
73 an
Bulgaria Ireland Thailand
/st
Chile Israel Turkey
s:/
Colombia Italy United Kingdom
tp
ht
Czechoslovakia Korea, Rep. of U.S.S.R.
France Netherlands Yugoslavia
Germany Poland
Hungary Portugal
The member body of the following country had expressed disapproval of the
document on technical grounds :
Canada
0 International Organization for Standardization, 1977 l
Printed in Switzerland
INTERNATIONAL STANDARD IS0 749-1977 (E)
Oilseed residues - Determination of total ash
1 SCOPE AND FIELD OF APPLICATION 5.5 Electrically I
heated muffle furnace, with air circulation
and capable of being controlled at 650 ? I5 “C.
This International Standard specifies a method for the
determination of the total ash from residues (excluding
compounded products) obtained by the extraction of oil
5.6 Desiccator, containing an efficient desiccant.
from oilseeds by pressure or solvent.
6 PROCEDURE
2 REFERENCES ) EW
Make all weighings to the nearest 0,001 g.
b-
ea
.ai VI
I SO 735, Oilseed residues - Determination of ash insoluble
77 2a
6.1 Preparation of the test sample
teh RE
19 a
in hydrochloric acid.
9- / 9d
6.1.1
s.i P
Take the
74 st contract sample obtained in accordance
IS0 771, Oilseed residues - Determination of moisture
o- /si
rd D
with IS0 5500.
/ i s ds
and volatile matter con tent.
da AR
d0 a r
99 /st :
a d
22 og ar d
an D
IS0 5500, Oilseed residues - Sampling. 1) 6.1.2
0a an
Grind the contract sample, if necessary, in the
(st AN
7 2 ta l d
previously well cleaned mechanical mill (5.2). First, use
-b c a a n
ST
dc i/ st
about one-twentieth of the sample to complete the cleaning
l
3 DEFINITION
9 b h. ul
of the mill, and reject these grindings; then grind the rest,
eh
1 - i te F
collect the grindings, mix carefully and carry out the
a
iT
total ash : The residue obtained after incineration at
analysis without delay.
550 + I5 “C under the operating conditions specified
5d s.
-4 r d
below.
e c da
6.2 Test portion
73 an
/st
6.2.1 Weigh the incineration dish (5.4), previously heated
4 PRINCIPLE
s:/
for I5 min in the furnace (5.5) at 550 + I5 ‘C, and allowed
tp
ht
Incineration of a test portion at 550 + 15 “C in an to cool in the desiccator (5.6) to laboratory temperature.
electrically heated muffle furnace, until practically constant
mass is reached. 6.2.2 Weigh into the incineration dish about 5 g of the
test sample (6.1.2), spread this uniformly over the whole
base of the dish and re-weigh.
5 APPARATUS
Carry out these operations as quickly as possible, in order
to avoid any appreciable change in moisture content.
5.1 Analytical balance.
NOTE - If the total ash is not
used subsequently for the determi-
5.2 Mechanical mill,
easy to clean and allowing the nation of the residue insoluble in hydrochloric acid (see IS0 735),
the test portion may be reduced to 2 g.
residues to be ground, without heating and without appreci-
able change in the moisture, volatile matter and oil content,
to particles passing completely through the sieve (5.3). 6.3 Determination
Place the dish containing the test portion on an electric
5.3 Sieve, with apertures of diameter I mm. hot-plate or over a gas flame, and heat progressively until
the test portion carbonizes, then place in the furnace (5.5),
5.4 Flat-bottomed incineration dish, of diameter about controlled at 550 + I5 “C. Continue heating until a white,
60 mm and height not exceeding 25 mm, of platinum, light grey or reddish ash is obtained, visibly free from
platinum-plated gold, silica or, if not available, porcelain. carbon particles (generally at least 2 to 3 h).
1) In preparation.
IS0 749-1977 (E)
Allow the d ish to cool in the desiccat or and weigh when it Take as the result the arithmetic mean of the two determi-
has reached labora tory temper nations, provided that the requirement concerning
repeatability (see 7.2) is satisfied. Otherwise, repeat the
Replace the dish in the furnace and continue heating for determination on two other test portions. If this time the
1 h at 550 + 15 “C. Allow the dish to cool and re-weigh, as difference again exceeds 0,2 g per 100 g of sample, take as
before. the result the arithmetic mean of the four determinations
carried out, provided that the maximum difference between
If the difference between the two weighings is less than or
the individual results does not exceed 0,5 g per 100 g of
equal to 0,002 g, regard the determination as finished. If
sample.
not, continue with 1 h periods in the furnace until the
difference between two successive weighings is less than or Report the result to one decimal place.
equal to 0,002 g.
If the ash is rather blackish after the first incineration of 2 9.1.2 If requested, the total ash may be expressed in
or 3 h, it may be moistened with a few drops of a 200 g/l relation to the dry matter by multiplying the result
solution of ammonium nitrate (not in excess so as to avoid obtained in accordance with 7.1 .I by
dispersion and sticking together of the ash). After drying in
100
an oven, resume the calcination. If necessary, repeat the
operation until incineration is complete. 100-u
Carry out two determinations on the same test sample. where U is the percentage by mass of moisture and volatile
matter determined as specified in IS0 771.
) EW
b-
ea
.ai VI
7.2 Repeatability
77 2a
teh RE
19 a
9- / 9d
7 EXPRESSION OF RESULTS The difference between the results of two determinations
s.i P
carried out simultaneously
74 st
or in rapid succession by the
o- /si
rd D
/ i s ds
da AR
7.1 Method of cakulation and formulae same analyst should not exceed 0,2 g of total ash per 100 g
d0 a r
99 /st :
of sample.
a d
22 og ar d
an D
0a an
7.1.1 The total ash yielded by the sample as received,
(st AN
7 2 ta l d
-b c a a n
expressed as a percentage by mass, is equal to
ST
dc i/ st
8 TEST REPORT
l
9 b h. ul
eh
1 - i te F
m2 -Iy)o The test report shall show the method used and the result
a
iT
x100 obtained, indicating clearly whether the result is expressed
“I -mQ
in relation to the product as received or in relation to the
5d s.
-4 r d
dry matter. It shall also mention any operating conditions
e c da
not specified in this International Standard, or regarded as
73 an
/st
m. is the mass, in grams, of the dish; optional, as well as any circumstances that may have
s:/
influenced the result.
tp
is the mass, in grams, of the dish and test portion;
ht
ml
The report shall include all details required for complete
m2 is the mass, in grams, of the dish and ash. iden tif icatio n of the samp le.