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fly Designation: C586 -19
Standard Test Method for
cordance wth intently scoped
veto rtermatol tanard ides sna Recommendations nse fy the Noid Trade OrsansatonTecnea Rarer Trade (11) Commie.
Potential Alkali Reactivity of Carbonate Rocks as Concrete
Aggregates (Rock-Cylinder Method)'
This standard sued unde he Hae! designation C586: the numer inmeatly following the designation inistes the year of
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1. Scope*
11 This test method covers the determination of the expan:
sion of a specimen of carbonate rock while immersed in a
solution of sodium hydroxide (NaOH) at room temperature.
‘The length changes occurring during such immersion indicate
the general level of reactivity of the rock and whether tests
should be made to determine the effect of aggregate prepared
from the rock upon the volume change in concrete
1.2 The values stated in SI units are to be regarded as
standard. No other units of measurement are included in this,
standard.
1.3 The text of this standard refers to notes and footnotes,
that provide explanatory material. These notes and footnotes,
(excluding those in tables and figures) shall not be considered
as requirements of this standard.
L4 This standard does not purport to address all of the
safety concerns, if any His the
responsibility of the user of this standard to establish appro-
priate safes, heaith, and environmental practices and deter
‘mine the applicability of regulatory limitations prior 10 use.
LS This international standard was developed in accor
dance with internationally recognized principles on standard:
ication established in she Decision on Principles for the
Development of International Standards, Guides and Recon:
‘mendations issued by the World Trade Organization Technical
Barriers to Trade (BT) Committe.
associated with its use
2. Referenced Documents
241 ASTM Standards:*
(€294 Descriptive Nomenclature for Constituents of Con-
crete Aggregates
"This to mth is ur the jruiction of ASTM Commitee CO on
Const sed Centee Aggro and ete dec posit of Sebcommiee
(COBO on Aspropate Reiter in Conte
ren edkionapprved Os. 1,209. Publis Noserber 2019, Originally
approved in 1066 Las! posi edion approved 2019 oe CS86-1(3019. BOI
oe eferoced ASTM staan, isthe ASTM wie, wasn oro
conact ASTM Comer Serice sect asm eg. Foe Anal Bon of AST
Stondants me craton flew th sans cent Say apo
(€205/C295M Guide for Petrographic Examination of Ag-
gregates for Conerete
CIOS Test Method for Length Change of Concrete Due to
Alkali-Carbonate Rock Reaction
D75/D75M Practice for Sampling Aggregates
1D1248 Specification for Polyethylene Plastics Extrusion
Materials for Wire and Cable
EI7T Practice for Use of the Terms Precision and Bias in
ASTM Test Methods.
3. Terminology
3.1 For definitions of terms relating to aggregates used in
this test method, refer to Descriptive Nomenclature C294,
4, Summary of Test Method
4.1 Small rock cylinders are immersed in 2 solution of
NaOH except when removed for determination of length
change. The length change of each specimen is periodically
determined,
5. Significance and Use
5.1 This test method is intended to give a relatively rapid
indication of the potential expansive reactivity of certain
carbonate rocks thal may be used as concrete aggregates. The
{est method has been successfully used in () research and (2)
preliminary screening of aggregate sources to indicate the
presence of material with a potential for deleterious expansion
when used in concrete
5.2 The test method is intended as a research and screening
‘method rather than as the basis fa specification requirement,
Iv is intended to supplement data from field service records,
petrographic examinations according to Guide C29S/C295M,
and tests of aggregate in concrete according to Test Method
cHios,
5.3 Alkalies participating in the expansive reactions with
aggregate constituents in concrete usually are derived from the
hydraulic cement; under certain circumstances they may be
derived from other constituents of concrete or from external
Two types of alkali reactivity of aggregates are
recognized: (/) alkalisilica reaction involving certain siliceous,
4 Summary of Changes section appears atthe end of this standardfly csa6 - 19
rocks, minerals, and anificial glasses, and (2) alkali carbonate
reaction involving dolomite in certain calcitic dolomites, do-
lomitic Timestones, and dolastones. This test method is not
suilable as 2 means to detect alkali-silica reaction.
6. Apparatus and Reagents
6.1 TN Sodium Hydroxide Solution—Dissolve 40 + | g of
reagent-grade sodium hydroxide (NaOH) in distilled water,
Uilue to | L and store in a polyethylene boule,
2 Sawing, Drilling, and Grinding Equipment, suitable for
preparing test specimens of the dimensions given in Section 8.
This will require one oF more rock saws, depending upon the
size of the original sample, a drill press equipped with a small
diamond core barrel for removing the cylindrical core, and a
lap, grinder, or suitable modified lathe for shaping the ends of
the specimens.
63 Storage Bottles, approximately 50 10 100-mL capacity
with caps and openings of sufficient size to facilitate removal
‘of specimens. The polyethylene bottle shall be selected to
ensue that the solution will not be modified by reaction with
the material composing the container, including pigments or
other additives or by transpiration of phases through the walls
‘of the container. Bottles with wall thickness not less than 0.50
‘mm and composed of high density polyethylene meeting the
requirements of Specification D1248 for materials of Type TI],
Class A. are suitable.
6A Lengsh Comparator for convenient and rapid measure
ment of lengths of specimens, the comparator shall be of such
design as to provide, permit, or include the following charac
terisies. One type of comparator which has been found
satisfactory is shown in Fig, 1
6.4.1 A positive means of contact with the conical ends of
the specimen to ensure reproducible measurement of length. A
variety of contact points have been used successfully, Care
should be exercised to ensure that when using specimens with
conical ends as described in 8.3. contact is made on the end
along a circle which is concentric about the long axis of the
specimen. If the measuring device is a barrel micrometer it
shall have a ratchet stop to produce a constant pressure on the
specimen,
6.4.2 A high-grade barrel or dial micrometer graduated to
read in 0.001 or 0.002-mm units, and accurate within 0.002
‘mm in any 0.020-mm range, and within 0.004 mm in any
0.200-mm range. The measuring device should be calibrated
‘throughout its range to determine both periodic and cumulative
errors for proper correction of observed data,
6.4.3 A sullicient range to allow for smal differences among
‘gage lengths of various specimens. If care is taken in the
fabrication of the specimens, a measuring device with a travel
(of not less than 7.5 mm provides ample range in the instrument,
and
(644 A standard or reference shall be used for checking the
measuring device at regular intervals, The bar that serves as a
reference for the length comparator shall have an over-all
length of 35 + 2 mm, The length of the bar shall be known to
fan accuracy of 0,002 mm, The bar shall be fused silica or a
steel alloy having a coefficient of thermal expansion not greater
than 1.0.x 10° °C. Each end shall be machined to the same
shape as that of the rock specimens. Ifa steel alloy is used, it
shall be polished (see Note 1). The reference bar shall be
placed in the insirument in the same position each time a length
‘measurement is made, The micrometer setting of the measur
ing device shall be checked by use of the reference bar at least
atthe beginning and end ofthe readings made within a half day
‘when the apparatus is kept in a room maintained at constant
temperature, It shall be checked more often when kept in a
room where temperature is not constant
Nore 1—Stet alloys wih low thermal expansion coeicient should not
be feu! weated because they Jose their low ‘coefficient of thermal
expansion when so treated
7. Sampling
7.1 Sample the rock in accordance with the applicable
requirements of Practice D75/D75M, except that the sample
‘mass of each discernable stratum shall be at least 1 kg, and
individual pieces shall be not less than 75 x 75 > 75 mm in
7.2 Sampling should be under the direction of an individual
capable of distinguishing differences in lithology. and the
sample of rock should be taken to represent only the particular
lithology under consideration bearing in mind the limitations
and significance of this method as stated in Section 5. Each
sample of rock should be in one piece of sullicient size for
preparing the necessary test specimens.
7.3 One test specimen will sufficiently represent the sample
of rock unless shale seams or other discontinuities are present
for the bedding is not discernible. In these cases, prepare and
test 3 mutually perpendicular specimens. OF these three
specimens. testing shall be continued on that one showing the
‘greatest calculated length change after 28 days of immersion in
alkali solution, Discard the remaining (wo,
8, Test Specimens
8.1 Test specimens shall be in the form of right circular
cylinders or square prisms with conical or plane parallel ends,
unless otherwise specified
8.2 The specimen shall have an over-all length of 35 * 5
mm and a diameter or sides of 9 1 mm for eylinders and
prisms respectively. Care shall be exercised in the preparation
Of the specimens to avoid alteration of the cylindrical surface
by polishing or with materials which will affect the rate of
cenity of alkali solution into the rock,
18.3 The included angle of the conical ends shall be approxi=
mately 120°,
‘844 Fabricate specimens having flat-end faces in such a
‘manner as 10 ensure thatthe faces are parallel 0 each other and
perpendicular to the major axis of the specimen (see Note 2),
Nowe faves parallel to each other and perpendicular 10 the
major axis ofthe specimen ean he made by turning the specimen na small
Tathe and using ool steel to cut the ends
9. Procedure
9.1 Place a position mark on the specimen to permit placing
the specimen in the comparator in the same position during
subsequent measurementslp ces - 19
Dil to press it
Imicrometer shaft
Specimen
Z Del and tap to
attach base plate
FIG. 1 A Typical Length Comparator
9.2 Measure the length of the test specimen.
9.3 Immerse the specimen in distilled water at a room
temperature in the range of 20 to 27.5°C.
94 At intervals, remove the specimen, blot 1 remove
excess surface water and measure until the change in length
uring a 24-h water immersion period does not exceed 0.02 4%
as calculated in 10.1. The length when in this condition is taken
ay the reference length. The reference length is usually
achieved alter 1 to 4 days oF immersion
9.5 Immerse the water-saturated specimens in a botle
containing a minimum of 35 mL of IN NaOH solution per
specimen at room temperature and seal. Immerse no more than
‘ovo specimens in a bottle,
9.6 Measure the length of the specimens afier 7, 14, 21, and
28 days of immersion in NaOH solution and at 4-wee
imervals thereafter. Ifthe tests continue beyond I year, make
intervals,fly c586- 19
9.7 When measurements are made, remove the specimen
from the bottle, rinse with distilled water, blot to remove
excess surface water and determine its length in the same
position as during the initial measurement
9.8 After measurement, immediately return the specimen to
the boitle and reseal
9.9 Replace the solution every 6 months during the testing
period
10, Calculation
10.1 Calculate the length change to the nearest 0.01 % of
the reference length as follows:
a= [th=
104} 100 a
4% length change at test age,
length in mm (in) at test age, and
y= reference length after equilibrium in water, as outlined
in 94.
11, Report
11.1. Report the following:
H1.ALL Identification number,
11.1.2 Type and source of rock.
11.1.3 Specimen shape and dimensions if other than right
circular eylinder,
11.1.4 Length change in percent to the nearest 0.01 % at
each time of measurement. Where no times of measurement are
specifically requested, data should be presented for at least the
following ages: I, 4, 8, and [6 weeks and the age at the final
‘measurement
1.1.5 Significant features revealed by examination of
specimen during and after storage in alkali solution, such as
cracking, warping, splitting, etc., and
11.1.6 Other significant information as deemed necessary,
such as petrographic and chemical analyses.
12, Preci
12.1 Precision:
12.1.1 IF the results of replicate specimens measured by the
same operator and which presumably represent the same
n and Bias
material, differ by more than 0.10 percentage point for expan-
sions less than 1.0 %, it is highly probable that the specimens
represent rocks that’ are significantly different in chemical
composition, texture, or both
12.1.2 The single-operator. single-comparator, single-
specimen precision has been found to be 0.02 perceniage
point (38) as defined in Practice E177.
12.1.3 The multi-operator, single-comparator, single-
specimen precision has een found 10 be 0.03 perceniage
point (35) as defined in Practice E177.
12.1.4 The multi-operator, multi-comparator, single-
specimen precision has been found to be +0.05 perceniage
point (3S) as defined in Practice E177.
12.15 Ina single laboratory, single operator study of the
range of expansion of pairs of rock cylinders from 29 samples
of rock from a single quarry (each pair of cylinders cut from a
different sample block approximately 75 x 75 x 50mm in
size), the following data were found:
12.1.5.1. For pairs of specimens giving average expansion of
less than 0.50 %, the average standard deviation was found 0
be 0.0255 %'; therefore, the difference in expansion between
pairs of cylinders cut from a single block should only exceed
0.072%" one time in twenty when the average expansion is
less than 0.50 %:
12.1.5. For pairs of specimens giving average expansion of
‘more than 0.50 “, the average standard deviation was found to
be 0.095 %*; therefore, the difference in expansion between
pairs of cylinders cut from a single block should only exceed
0.269 4" one time in twenty when the average expansion is
‘more than 0.50 %
12.2. Bias—The procedure in this test method for measuring
expansion has no bias because the expansion can he defined
only in terms of this test method.
13, Keywords
13.1 aggregate; alkali reactivity: carbonate rocks; conerete:
deleterious expansion
Pracice CD, i
APPENDIX
(Nonmandatory Information)
xt
XI. Since the expansion caused by reactions between
cement alkalies and carbonate aggregates is sensitive to subtle
changes in aggregate lithology. the results of measurements
should be interpreted with full recognition of the variables
‘which would affect the results obtained. The acceptance or
rejection of aggregate sources based solely on the results of this
test is not recommended since, in commercial production,
expansive and nonexpansive materials may occur in close
INTERPRETATION OF RESULTS
proximity and the securing of samples adequately representa-
tive of the variability of the production of the source is a
difficult task and requites the efforts of an individual trained to
istinguish differences in lithology.
X1.2 The relationship of the test results to the behavior of
large quantities of rock from a given source will depend upon
the degree to which the petrographic and chemical properties
of the rock vary within the source.Aly csas - 19
X1.3 Research results have indicated that the expansive
behavior of agaregate in concrete is qualitatively predicted by
the resulis of the rock eylinder test. Quantitative prediction of
the expansion of concrete containing reactive aggregate de-
pends upon (J) the degree of aggregate reactivity, (2) the
mount of reactive constituent, (3) the alkali content of the
cement, and (4) the environment. Appreciate expansion
should indieate the need for further testing. In the light of
current knowledge. it appears that expansions in excess of
0.10 % are indicative of chemical reaction and should warrant
additional testing preferably in concrete using Test Method
C1105. Usually expansive tendencies are evident afier 28 days,
of immersion in alkali, however, exceptions to this have been
noted. Deleterious expansion of conerete appears to depend
tupon the magnitude and rate of aggregate expansion and the
time at which it begins: however, quantitative predictions of
concrete expansion in service solely from results of this test
method are not possible,
SUMMARY OF CHANGES
Committee CO9 has identified the location of selected changes to this standard since the last issue
(C586-11(2019)) that may impact the use of this standard, (Approved Oct. 1, 2019.)
(1) Section 1.3 was added to notify users that notes and
footnotes are non-mandatory.
ASTI ntorationsl takes no poston respecting the vlc cf any patent hs asserted in connecon wih any em mentioned
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