BS598 Part 101
BS598 Part 101
BS598 Part 101
Sampling and
examination of
bituminous mixtures
for roads and other
paved areas —
Part 101: Methods for preparatory
treatment of samples for analysis
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BS 598-101:2004
Contents
Page
Committees responsible Inside front cover
Foreword ii
1 Scope 1
2 Definitions 1
3 Preparatory treatment of samples of bituminous mixtures 1
Table 1 — Temperature of the oven for reheating samples prior to sample
reduction 2
Table 2 — Mass of material for each determination 3
Publications referred to 5
Foreword
Summary of pages
This document comprises a front cover, an inside front cover, pages i and ii
pages 1 to 5 and a back cover.
The BSI copyright notice displayed in this document indicates when the
document was last issued.
1 Scope
This part of BS 598 describes the methods for preparatory treatment necessary to provide test samples of
bituminous mixtures and coated chippings, but excluding mastics and slurry seal, that have been delivered
in bulk to the testing laboratory for analysis.
NOTE The titles of the publications referred to in this standard are listed on the inside back cover.
2 Definitions
For the purposes of this part of BS 598, the definitions given in BS 598-100 apply.
3.3.3 Surface dressings. Remove any surface dressing if possible. Report the presence of any visible
penetration of the surface dressing binder into the sample.
3.3.4 Tack coat or blinding grit. Report the presence of any tack coat or blinding grit.
3.3.5 Fractured aggregate. Report the presence of any fractured aggregate caused by sampling but do not
remove such aggregate.
3.3.6 Multicourse sample. If possible, use a circular stone cutting saw to separate courses, particularly
within core samples. In situations where this approach and other physical methods of cold separation are
impractical, adopt the following procedure.
Lay the sample upside down on a clean sheet metal tray and warm sufficiently in a conventional oven just
to soften the material so that the courses may be separated.
NOTE 1 In some cases insertion at the interface of the courses of a paint stripping knife with a wide blade, or similar tool, will assist
in the separation.
NOTE 2 Only in cases of extreme necessity should the separation of the courses of a sample that has broken be attempted. In such
cases if separation by hand picking is attempted, test results will be unreliable and this should be clearly stated in the test report.
3.3.7 Free water. If free water is visible on the sample, or if the sample feels wet to the touch or if there is
any reason to suppose that the sample may contain water that is unevenly dispersed, break the sample into
pieces, by warming if necessary, of such a size that the water can readily evaporate. Leave the broken
sample exposed in a thin layer on a clean, hard surface, in a warm laboratory for at least 24 h. Then treat
the sample as described in 3.4 or 3.5, as appropriate.
NOTE This process is not suitable if the determination of water content is required (see 3.2).
3.3.8 Binder drainage. Report if any binder drainage has occurred and collect and weigh the drained
material. When the sample has been reduced to a suitable size for testing (see 3.4), add a proportionate
representative weighed fraction of the drained material to the portion to be tested. Record if the drained
material cannot be collected.
3.4 Heat treatment before sample reduction
3.4.1 Heat samples that cannot be remixed by hand in accordance with 3.4.2 or 3.4.3.
3.4.2 Heat the entire sample or separated course in a suitable conventional oven at a temperature not
exceeding the appropriate value given in Table 1 until it is just sufficiently soft to be readily mixed and
divided. Do not leave the sample in the oven for more than 4 h.
NOTE The temperature constraint is to minimize loss of the volatile constituents of the binder.
3.4.3 Heat the sample in increments in a suitable microwave oven and at no time allow the temperature of
the oven to exceed the appropriate value given in Table 1.
WARNING. Do not place any metal objects, e.g. containers or trays, in a microwave oven.
Keep the heating time to a minimum (5 min is usually sufficient).
NOTE 1 Care should be exercised when using this microwave method as large aggregate particles may split.
NOTE 2 After heating in the microwave oven the increments awaiting bulking may be held in a conventional oven, subject to the
time and temperature constraints given in 3.4.2.
NOTE 3 This microwave method is not suitable if the determination of water content is required (see 3.2).
Table 1 — Temperature of the oven for reheating samples prior to sample reduction
Type of binder in sample Nominal characteristic of binder in sample Maximum temperature of oven
°C
Bitumen and Less than 200 s at 40 °C 60
cut-back bitumena 200 s to 500 s at 40 °C 70
Greater than 250 penetration at 25 °C 80
160-220 penetration at 25 °C 100
70 to 150 penetration at 25 °C 120
30 to 70 penetration at 25 °C 140
Less than 30 penetration at 25 °C 160
NOTE If modified binders are used the temperatures for reheating samples should be in accordance with supplier’s
recommendations.
a See BS EN 12597 for explanation of terms.
3.5 Sample reduction for the determination of water content, binder content and grading
3.5.1 Weigh the whole of the sample, or each portion representing the separate courses, and place on a clean
hard surface, e.g. a sheet metal tray. Mix the sample thoroughly and reduce it to the quantity required for
test, as given in Table 2, either by using a riffle box, which may be heated or slightly oiled, in accordance
with 9.2 of BS EN 932-1:1997 or by quartering as described in 3.5.2, 3.5.3 and 3.5.4.
NOTE 1 The use of a riffle box for mixtures with D of 20 mm and larger is likely to be quicker and will provide a sample of accuracy
equal to or greater than that obtained by quartering.
NOTE 2 By assuming equal subdivision of the sample after each quartering process it is possible, by weighing the original sample,
to estimate whether the mass remaining after quartering will be within the appropriate range given in Table 2. If the estimated mass
is above the upper limit of the appropriate range given in Table 2 the mass of the original sample may be reduced by one quarter. This
should be done by quartering twice, rejecting two opposite quarters from the second quartering process, combining the remainder from
the second quartering process with the material put aside from the first quartering process and then carrying out the procedure
described in 3.5.2 to 3.5.3.
3.5.2 Mix the sample thoroughly by heaping it into a cone and turning it over to form a new cone three times
as described as follows.
Form a conical heap by depositing each shovelful of the material on the apex of the cone. Distribute any
material that rolls down the sides as evenly as possible, so that the centre of the cone is not displaced. Push
back to the edge of the heap any larger pieces of aggregate that may scatter round the base.
Table 2 — Mass of material for each determination
Type of material D Mass of sample for each determination
mm g
Bituminous mixture >32 3 000 to 5 000
32 2 500 to 3 500
20 1 000 to 2 000
14 800 to 1 600
10 500 to 1 000
6 300 to 600
k4 250 to 500
Coated chippings All sizes 2 000 to 3 000
3.5.3 Flatten the third cone formed from the mixed sample by repeated vertical insertions of the edge of a
shovel or board, commencing about the centre and working progressively round the cone, lifting the shovel
or board clear of the material after each insertion.
Ensure that the heap thus formed is reasonably uniform in thickness and diameter and that its centre
coincides with the centre of the cone from which it was produced.
3.5.4 Quarter the heap along two diameters that intersect at right angles. Combine one pair of diagonally
opposite quarters and discard the remainder.
3.5.5 Repeat 3.5.2, 3.5.3 and 3.5.4 until the mass remaining is about four times the mass of the sample
required for the test. Then, repeat 3.5.2, 3.5.3 and 3.5.4 once more and set aside for the estimations of
water content the quarters that would otherwise be discarded. However, if the water content is to be
calculated using the hot extractor method discard these quarters.
NOTE 1 The use of a quartering cross of wood or sheet metal, which can be forced through the heap, often facilitates quartering in
cases where the material tends to segregate.
NOTE 2 If drained binder was collected during the earlier treatment of the sample (see 3.3.8), a proportionate amount of binder
should be added to the samples taken for test.
Publications referred to
Standards publications
BS 598-100:2004, Sampling and examination of bituminous mixtures for roads and other paved areas —
Methods for sampling for analysis.
BS 5284:1993, Methods — Sampling and testing mastic asphalt and pitchmastic used in building.
BS EN 932-1:1997, Tests for general properties of aggregates, Part 1 — Methods of sampling.
BS EN 12597:2000, Bitumen and bituminous binders — Terminology.
PD 6682-2:2003, Aggregates — Part 2: Aggregates for bituminous mixtures and surface treatments for
roads, airfields and other trafficked areas — Guidance on the use of BS EN 13043.
PD 6682-9:2003, Aggregates — Part 9: Guidance on the use of European test method standards.
Other documents
[1] GREAT BRITAIN. Health and Safety at Work etc. Act 1974. London: The Stationery Office.
[2] GREAT BRITAIN. The Factories Act 1961. London: The Stationery Office.
[3] GREAT BRITAIN. The Construction Regulations Act 1961. London: The Stationery Office.
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