Sans 5839
Sans 5839
Sans 5839
This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
The standard must reside on an internal network or intranet and may only be used for reference purposes in compliance with SABS
copyright rules. The standard or parts thereof may not be distributed in any form without permission from the SABS.
ISBN 978-0-626-21776-1
SANS 5839:2008
Edition 2.2
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
The standard must reside on an internal network or intranet and may only be used for reference purposes in compliance with SABS
copyright rules. The standard or parts thereof may not be distributed in any form without permission from the SABS.
SANS 5839:2008
Edition 2.2
Table of changes
Change No. Date Scope
Amdt 1 2002 Amended to update normative references.
Amdt 2 2008 Amended to change the designation of SABS standards to SANS
standards, with no technical changes.
Foreword
This South African standard was approved by National Committee StanSA SC 5120.61A, Construction
standards – Cement, lime and concrete, in accordance with procedures of Standards South Africa, in
compliance with annex 3 of the WTO/TBT agreement.
This document was published in July 2008. This document supersedes SABS SM 839:2002
(edition 2.1).
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
The standard must reside on an internal network or intranet and may only be used for reference purposes in compliance with SABS
copyright rules. The standard or parts thereof may not be distributed in any form without permission from the SABS.
SANS 5839:2008
Edition 2.2
Contents
Page
Foreword
3 Reagents ................................................................................................................................ 3
4 Apparatus ............................................................................................................................... 4
6 Procedure ............................................................................................................................... 5
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
The standard must reside on an internal network or intranet and may only be used for reference purposes in compliance with SABS
copyright rules. The standard or parts thereof may not be distributed in any form without permission from the SABS.
SANS 5839:2008
Edition 2.2
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
The standard must reside on an internal network or intranet and may only be used for reference purposes in compliance with SABS
copyright rules. The standard or parts thereof may not be distributed in any form without permission from the SABS.
SANS 5839:2008
Edition 2.2
In the case of crushed aggregate, it is recommended that specimens prepared for testing (see 5.2) be
examined under magnification for cracks caused by stresses induced during crushing. Penetration of the
sulfate solution into such cracks could cause disruptive forces, resulting in a faulty impression of the
soundness or integrity of the aggregate.
2 Normative references
The following standards contain provisions which, through reference in this text, constitute provisions of
this standard. All standards are subject to revision and, since any reference to a standard is deemed to
be a reference to the latest edition of that standard, parties to agreements based on this standard are
encouraged to take steps to ensure the use of the most recent editions of the standards indicated below.
Information on currently valid national and international standards can be obtained from Standards
South Africa.
SANS 201, Sieves analysis fines, content and dust content of aggregates.
SANS 3310-1/ISO 3310-1, Test sieves – Technical requirements and testing – Part 1: Test sieves of
metal wire cloth. Amdt 1
SANS 3310-2/ISO 3310-2, Test sieves – Technical requirements and testing – Part 2: Test sieves of
perforated metal plate. Amdt 1
3 Reagents
3.1 Water
Distilled or deionized water.
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
The standard must reside on an internal network or intranet and may only be used for reference purposes in compliance with SABS
copyright rules. The standard or parts thereof may not be distributed in any form without permission from the SABS.
SANS 5839:2008
Edition 2.2
4 Apparatus
4.1 Test sieves, that comply with the requirements of SANS 3310-1 or SANS 3310-2. Amdt 1
4.2 Cloth, or wire mesh basket, of aperture size not exceeding 150 µm.
5.1.1 From a sieve analysis of the aggregate (conducted in accordance with SANS 201), determine
which of the size fractions given in table 1 each represents more than 5 % (by mass) of the aggregate.
From the test sample (see SANS 197), take a mass that is estimated to contain at least 100 g of each of
those fractions.
1 2
µm
Passing Retained
9 500 4 750
4 750 2 360
2 360 1 180
1 180 600
600 300
5.1.2 Remove all fine adhering material by washing the aggregate on a sieve of aperture size not
exceeding 300 µm. Dry the material retained on the sieve at a temperature of 100 °C to 110 °C until the
decrease in mass after two successive drying periods of 4 h does not exceed 0,1 % of the total mass.
Cool to room temperature in a desiccator.
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
The standard must reside on an internal network or intranet and may only be used for reference purposes in compliance with SABS
copyright rules. The standard or parts thereof may not be distributed in any form without permission from the SABS.
SANS 5839:2008
Edition 2.2
5.1.3 Isolate the relevant fractions by using the appropriate sieves and sieving until no more aggregate
passes each of these sieves. From each of these fractions (but excluding particles lodged in the
apertures of the sieves), take a test specimen of mass approximately 100 g and wrap each test
specimen (separately) in cloth or put it into a suitable wire mesh basket (see 4.2).
5.2.1 From a sieve analysis of the aggregate (conducted in accordance with SANS 201), determine
which of the size fractions given in table 2 each represents more than 5 % (by mass) of the aggregate.
From the test sample (see SANS 197) take a mass that is estimated to contain at least the appropriate
minimum quantities given in column 3 of table 2 of each of these fractions.
1 2 3
5.2.2 Remove all fine adhering material by washing the aggregate on a sieve of aperture size not
exceeding 4 750 µm. Dry the material retained on the sieve at a temperature of 100 °C to 110 °C until
the decrease in mass after two successive drying periods of 4 h does not exceed 0,1 % of the total
mass. Cool the sample to room temperature in a desiccator.
5.2.3 Isolate the relevant fractions by using the appropriate sieves and sieving until no more aggregate
passes each of these sieves. (Fit particles larger than 9,5 mm individually through the sieve apertures by
hand but do not use excessive pressure to force aggregate through.) From each of these fractions (but
excluding particles lodged in the apertures of the sieves), take a test sample of the appropriate mass
(see table 2) and wrap each test specimen (separately) in cloth or put it into a suitable wire mesh basket
(see 4.2).
6 Procedure
NOTE Carry out steps 6.1 to 6.3 without removing the specimens from their cloth wrapper or wire mesh basket.
6.1 Place each test specimen in a separate container, add enough of the magnesium sulfate solution to
cover the specimen and leave it immersed for at least 16 h, maintaining the temperature of the solution
at 22 °C to 24 °C. Remove the test specimens from the solution and allow them to drain for
approximately 10 min and, in the case of a specimen that is wrapped in cloth, place the wrapped
specimen on a wire mesh tray, open the cloth, and spread the material out on the cloth, taking care that
no material is lost.
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
The standard must reside on an internal network or intranet and may only be used for reference purposes in compliance with SABS
copyright rules. The standard or parts thereof may not be distributed in any form without permission from the SABS.
SANS 5839:2008
Edition 2.2
6.2 Dry the specimens for at least 8 h in a well ventilated oven maintained at a temperature of
100 °C to 110 °C. Remove the specimens from the oven at the end of the drying period, and allow them
to cool to room temperature. This process of immersion in magnesium sulfate solution followed by drying
and cooling constitutes one cycle of the soundness test.
6.3 Repeat the procedures described in 6.1 and 6.2 for the number of cycles considered necessary.
6.4 After completion of the final cycle, transfer each specimen from its wrapper to a beaker and wash
the specimen until the washings are free from magnesium sulfate (as proved by the washings' no longer
causing barium sulfate to be precipitated from an aqueous solution of barium chloride). Dry each
specimen until the decrease in mass after two successive drying periods of 4 h does not exceed 0,1 %
of the total mass. Cool the specimens to room temperature in a desiccator.
6.5 In the case of fine aggregate, sieve each specimen on the same sieve as that on which it was
retained in its preparation and continue sieving until no more material passes the sieve. In the case of
coarse aggregate, sieve each specimen as described in 5.2.3 but use a sieve of the appropriate
aperture size given in column 3 of table 3.
Dimensions in millimetres
1 2 3
6.6 Determine the mass of the material retained on each sieve and calculate the percentage loss for
each fraction tested.
7.1 Calculate the percentage representative loss RL for each fraction tested as follows:
A×B
RL =
100
where
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.
The standard must reside on an internal network or intranet and may only be used for reference purposes in compliance with SABS
copyright rules. The standard or parts thereof may not be distributed in any form without permission from the SABS.
SANS 5839:2008
Edition 2.2
B is the percentage representation of the fraction tested as determined in 5.1.1 or 5.2.1, as relevant,
(but, in the case of a fine aggregate in which the fractions larger than 4 750 µm represented more
than 10 % (by mass) of the aggregate, use 10 % as the value of B).
7.2 For each fraction that had a representation not exceeding 5 % (and that was, therefore, not tested),
use the average of the values of RL for the next smaller and next larger fractions tested and in the case
of the coarsest or finest fraction, use the value for the next smaller or next larger fraction, as relevant
(except that, in the case of fine aggregate, it is impracticable to test sizes finer than 300 µm, since these
are considered to have no loss).
7.3 Record and report the percentage loss of the test sample, and the sum of individual values of RL to
the nearest 1 %, calculated as described in 7.1 and 7.2.
© SABS. This non-printable standard is exclusively for approved users of the SABS’ Complete Collection of Standards and Related Documents.