Is 1727 PDF

IS : 1727 - 1967
( Reaffirmed 1999 )
Indian Standard
METHODS OF TEST FOR
POZZOLANIC MATERIALS
(First Revision)
Sixth Reprint OCTOBER 1996
UDC 666.95.014/.017 : 691.545
0 Copyright 1968
BUREAU OF INDIAN STANDARDS
MANAK BHAVAN, 9 BAHADUR SHAH ZAFAR MARG
NEW DELHI 110002
Gr 10 February 1968
Indian Standard
METHODS OF TEST FOR
(First Revision)
Pozzolanas Sectional Committee, BDC 16
Ctilmfln Represmting
Dn R. R. HA~IAN~~I The Associated Cement Companies Ltd, Bombay
DR IQBALAU Hyderabad Engineering Research Laboratory,

Hydcrabad
Sxm B. C. BANERJEB Directorate General of Technical Development
( Ministrv of Industrv I
SHRI M. J. BHATT Hindustan S&cl Ltd, Ranchi
SHIU S. N. BANERJEE ( Altematc j
SHRI K.V. CI~AUBAL Federation of Electricity Undertakings of India,
Bombay
Dn S. K. CHOPRA Central Buildinu Research Institute (. CSIR 1.
Roorkee -
SHRI A. K. CHAITERJEE ( Alternate )
I)r I. c. Des M. PAI8 CUDDOU Central W’ater & Power Commission, New Delhi
SHRI N. C. RAWAL ( Alkmalc )
SBllc.c.D~l National Test House; Calcutta
SHRI N. C. SENCUPI’A ( Al&mate )
DEPUTY DIRECTOR RESEARUI Railway Board
&$0; Irrigation & Power Research Institute, Amritur

WRI MOHINIXR SING~X( Altcrnatc )
I)IILECTOR Maharashtra Engineering Research Institute, Nasik
SHRI M.R. VINAYAKA (Alftmuk)
DXRECTOR, hsPEm0~ AND Bhakra Dam, Nangal Township
CONTROL
SHRI C. C. GIJ?TA U.P. PWD Research Institute, Lucknow
SHRI V.K.GUF+'TA Engineer-in-Chief’s Branch, Army Headquarters
Paor S. R. M~HRA CentraihZoad Research Institute ( CSIR), New
DR R. K. Grxosrs ( Afferna~ \
&RI K. K. NAYBL+R ’ ’ Concrete Association of India, Bombay
SHRI P. J. JAGIJIJ
( Abmatu )
SHRl \‘. N. PA1 The Associatrd Cement Companies Ltd. Bombay
fiI3sU RABINDER SINGH National Buildings Oraanizaiion I Minirtrv of Works.
Housing & Urb& Development ) .
Smu C. T. BODE ( AI&raak )
( Cbntinurd on pug8 2 )

MANAK BHAVAN, 9 BAHADUR SHAH ZAFAR MARG
NEW DELHI 110002
Isrl727-1967
( Gmtinued from
jmgc
1)
MrmbaJ RqWscnring
SHRIR. R. SUKHRANI Kaudla Port Project ( Ministry of Traqort )
SUPERINTENDING ENGINEERIrrigation Department, Govemmcut of Madras
(-ou)
SUPERXNTENDING GEOLOGIST
(EG Geological Survey of India, Calcutta
&GW)
SUPERINTENDING SURVEYOR OF Central Public Works Department
WORKS(I)
DR H. C. VIS~ESVARAYA Canent Rcaearch Institute of India, New D&i
SHRXR. NAGARAJAN, Director General, ISI ( Ex-oficcioMember)
Director ( Civ Engg )
SHRIY. R. TANEJA
Deputy Director ( Civ Engg ), IS1
SHRI DI&PAKBANDYOPADHYAY
Senior Technical Assistant ( Civ Engg ), IS1
Panel for Revision of IS : 1727-1960, BDC 16/Pl
Convener
DR H. C. VISYZSVARASA Cement Research Institute of India, New Delhi
Members
I.h IQBAS. ALI Hyderabad Engine,-ring Research Laboratory,
Hyderabad
DR S. K. C~OPRA CentR~or~e~lding Research Institute ( CSIR ),
SHRI C. A. TAN~JA( Alternate )

DR R. K. GAOSH Centbt,hZoad Research Institute ( CSIR), NCW
Sriar P. J. JAGUS Concrete Association of India, Bombay

SrrrtrM. R. VINAYAU Maharaahtra Engineering R-arch Institute, Nasih
2
Is:172711967
Indian Standard
METHODS OF TEST FOR
f First Revision)
0. FOREWORD
0.1 This Indian Standard ( First Revision ) was adopted by the Indian
Standards Institution on 24 July 1967, after the draft finalized by the
Pozzolanas Sectional Committee had been approved by the Civil Engineering
Division Council.
0.2 This standard was originally published in 1960. The various provisions
of the standard have been under the review of the Pozzolanas Sectional
Committee, for quite some time. Th e greater utilization of pozzolanic
materials in the country, the experience with the use of this standard and also
the latest developments in the field of pozzolanic materials has necessitated
a change in the approach to the testing of pozzolanas. In the light of these,
the Pozzolanas Sectional Committee has felt the need to issue this revision, to
incorporate the modification necessary to bring the standard in line with the
present thinking on the subject.
0.2.1 The revision incorporates a number of changes, the most important
of them being - the method of test for specific surface of pozzolana by Blaine
air permeability apparatus, the use of revised grading of standard sand for
various tests, introduction of ‘ absolute volume ’ concept for the test mixtures
for various pozzolanic activity tests, modified method of compaction of test
specimens and a test for specific gravity of pozzolanas.
0.2.2 The design of mix for various pozzolanic activity tests on absolute
volume basis was considered preferable as this would keep the binder plus
pozzolana volume same as that of binder paste volume in control mix. This
will control the workability, voids and yield of mortar which are affected by a
change in the specific gravity of pozzolanas. If the proportions are by
weight alone, any change in the specific gravity of pozzolana will alter
the water requirements for the mix and this will have a significant effect
on the strength with the result that a true assessment of the quality of
pozzolana would not be possible. Proportioning by weight will also not
give true comparison between the reactivity of two different pozzolanas
because even if they had equal efficiency in respect of their chemical reactiv-
ity, an artificial difference in the strength will be observed due to difTe-
rence in their specific gravities in case of proportioning by weight; on the
other hand, if the absolute volumes occupied by both pozzolanas were kept
r-------- ~
IS : 1727- 1967
constant ( by batching by absolute volume ) such an anomaly would not

occur.
0.2.3 Instead of equating workability on the basis of water requirements
in a cement pozzolana paste, a suitable method to judge the performance
of qualitative workability basis relative to the control mix has been intro-
duced both for lime reactivity test as well as compressive strength test of
cement pozzolana mortars. The Sectional Committee was of the view
that the determination of water requirements merely on cement paste as
specified earlier in the standard may not have sufficient bearing in reflecting
the true workability of mortar because the workability and water require-
ments in cement mortar may be effected by the finer fractions of pozzolana
reducing the particle friction in various sizes of sand grains.
0.3 There are different kinds of pozzolanas used for different purposes in
various construction works. In general, pozzolanas improve certain
properties of concrete, such as workability, cohesiveness, impermeability,
resistance to aggressive waters and also assist in the reduction of heat of
hydration and alkali-aggregate reactivity in hardened concrete. The relative
importance of each of these properties will naturally depend upon the type
and nature of construction. In mass concrete construction, for example,
improvement in workability, reduction of segregation and low heat of
hydration are relatively more important. In hydraulic structures imper-
viousness is of very great importance. Resistance to attack by acids and
sulphate waters is necessary in marine construction in sewage disposal w&s
and in laying roads over sulphate bearing soils.
0.4 While the only pozzolana which has been extensively used for centuries
in this country is SURKHI or burnt clay pozzolana; the rapid industrializa-
tion of the country is yielding large quantities of industrial wastes, like
fly ash, coal ash, etc, which form additional sources for pozzolanas. The
use of fly ash as a pozzolana is well established in a number of countries
abroad, but it has come in vogue in India only recently. Besides thefe,
there are a large number of pozzolanic clay deposits of stained and impure
kaolins, ferruginous or ocherous earths, altered laterites and bauxites, certain
shales, etc, available in different parts of the country, which yield highly
reactive pozzolanic materials. The Central Road Research Institute,
New Delhi have conducted an all India survey of pozzolanic clay deposits
through the length and breadth of the country and prepared detailed report
of such deposits in each State with suggestions for the mode of industrial
utilization of each of them. The Sectional Committee has already pub-
lished IS : 1344-1959*, IS : 3812 ( Part I )-19667, IS : 3812 ( Part II )-19662
and IS: 3812 ( Part III )-19665. This standard lays down the methods of
test for pozzolanic materials with a view to providing a uniform basis for the
*Specification for SURKHI for use in mortar and concrete. ( Since revised 1.
tbpccification for fly ash: Part 1 For use as pozzolana.
$Sperification for fly ash: Part 11 For use as admixture for concrete.
fSpcci6cation for fly ash: Part III For use as fine aggregate for mortar and concrete.
rS:1727-1967
assessment of the propert& and potentialities of the different poz~olani~

materials.
0.5 The tests to be performed on any particular pozzolanic material.would
depend on the purpose for which it is to be used and it is not necessary that
all the tests should be performed on every pozzolatia.
0.5.1 Though considered desirable, the test for mortar bar expansion to
indicate reduction of alkali-aggregate reactivity has been omitted from this
standard for two reasons; namely, there are very few localities in India
where alkali-reactive aggregates would be encountered and the problem is
not so serious as it is in some other countries, and the mortar bar test rep-
quires strictly controlled conditions whith are available only in a few labo-
ratorics, and any lack of control might easily give misleading results.
0.6 In the formulation of this standard due weightage has been given
to international co-ordination among the standards and practices prevaihng
in different countries in addition to relating it to the practices in the field
in this country.
0.7 This standard requires reference to the following Indian Standards:
IS : 196-1966 Specification for atmospheric conditions for testing
( reazsrd )
*IS : 269-1958 Specification for ordinary, rapid-hardening and low
hesqt Portland cement ( revised)
IS : 460- 1962 Spetification for test sieves ( revised)
IS : 516-1959 Methods of test for strength of concrete
IS : 650- 1966 Specification for standard sand for testing of cement
(Jirst revision )
*IS : 712-1964 Specification for building limes ( revised)
IS : 1199-1959 Methods of sampling and analysis of concrete
IS : 1607- 1960 Methods for dry sieving
0.8 For the purpose of deciding whether a particular requirement of thii
standard is complied with, the final value, observed or calculated, expressing
_the result of a test or analysis, shall be rounded off in accordance with
$IS : 2-1960*. The number of significant places retained in the rounded
off value should be the same as that of the specified value in this standard.
1. SCOPE
1.1 This standard covers the following tests for pozzolanic materials:
a) Chemical analysis,
b) Fineness,
c) Soundness,
- ~Sice revis&.
,tRula for roundirlg off numerical valua ( r&red).
5
rs : 1727 - 1967
d) Setting time,
e) Lime reactivity,
f) Compressive strength,
g) Transverse strength,
h) Drying shrinkage,
j) Permeability,
k) Reduction in alkalinity and silica release, and
m) Specific gravity.
2. TERMINOLOGY
2.1 For the purpose of this standard, the definition of terms given in
IS : 4305-1967* shall apply.
3. TEST MATERlALS
3.1 Hydrated Lime - Hydrated lime for use in the tests shall conform to
the requirements for hydrated fat lime ( Class C ) of IS : 712-1964t and also
to the following additional requirements:
a) The calcium compound present in lime calculated as calcium oxide
shall not be less than 90 percent by weight of the ignited sample.
b) The residue on 212-micron IS Sieve ( see IS : 460-1962$ ) shall not
be more than two percent by weight.
3.2 Cement -Cement for use in the tests shall be ordinary cement con-
forming to IS : 269-1958s.
3.3 Standard Sand - Standard sand for use in the tests shall conform to
IS : 650-196611.
4. TEST CONDITIONS
4.1 Temperature and Relative Humidity - Unless otherwise specified
the temperature range within which physical tests may be carried out should
be, as far as possible, 27 f 2°C and the relative humidity 65 f 5 percent
(see IS : 196-1966g ).
5. CHEMICAL ANALYSIS
5.1 Reagents
5.1.1 Quality of Reagents-Unless otherwise specified, pure chemicals
and distilled water (see IS : 1070-1960** ) shall be used in the test.
NOTE- Pure chemicals shall mean chemicals that do not contain impurities which
affect the results of the analysis.
*Glossary of terms relating to pozzolanas. ( Since revisc0
tSpecification for building likes ( revised ) .
SSpecification for test sieves ( rcuised ) .
&ecification for ordinary, rapid-hardening and low heat Portland cement ( & ).
Since revised ).
@pecification for standard sand for testing of cement (/;rst rwition ).
~Specification for atmospheric conditions for tekting ( retied).
l *Specification forwater, distilled quaUty ( tied ).
6
IS:1727-1963
,S.1.2The following reagents and special solutions are required:

a>Reagents
Hydrochloric acid -sp gr 1.16
Nitric acid -sp gr 1.42
Sulphuric acid -sp gr 1.84
Phosphoric acid, -sp gr 1.7
Hydrofluoric acid - 40 per cent
Ammonium hydroxide - sp gr 0.90
NOTE- The reagents shall be of the analytical reagent quality.
b) Dilute solutions of reagents - Prepare the following solutions by
diluting the reagent with distilled water:
Hydrochloric acid - 50 percent, 25 percent and one percent ( v/v)
Nitric acid - 3 percent ( v/v)
Ammonium hydroxide - 50 percent ( v/v)
4 Stannous chloride solution-Dissolve 50 g of stannous chloride
in 100 ml of hflrochloric &id and dilute to one litre. Keep a
few pieces of pure metallic tin in contact with the solution.
4 Mercuric chloride solution-Prepare a saturated solution by dissolving
5.6 g in 100 ml of water at room temperature.
4 Manganese sulphate solution - Dissolve 35 g of crystalline manganese
sulphate in 250 ml of distilled water. Add 70 ml of phosphoric
acid ( sp gr 1.7 ) and 65 ml of sulphuric acid ( sp gr 1.84 ). Dilute
to 500 ml.
f> Standurd potassium permanganate solution - Approximately 0.05 N.
Dissolve about l-5 g of potassium permanganate in one litre of
distilled water. Allow to stand for a week; filter through asbestos
mat and keep in a dark place after standardizing it with pure
sodium oxalate.
g) Ammonium nitrate solution - Dissolve 2 g of ammonium nitrate in
100 ml of water.
h) Ammonium oxalate solution - Dissolve 50 g of ammonium oxide in
one litre of water. Also prepare a dilute solution containing one
gram of salt per litre.
j> Ammonium hydrogen phosphate solution - Dissolve 250 g of ammonium
hydrogen phosphate in one litre of water.
4 Barium chloride solution - Dissolve 100 g of barium chloride in one
litre of water.
5.2 Preparation ofsamplefor Analysis- About 1OOg ofthe represen-
tative sample shall be air-dried and ground to pass 150-micron IS Sieve.
The material shall be stored in an air-tight bottle.
7
U[Ir1727-1967
53 LossonIgnition
5.3.1Ignite I.00 g of the air-dried, finely ground sample in a platinum
crucible of 20 to 25 ml capacity by placing it in a muffle furnace at
1000 f 25°C to constant weight ( for about 20 to 30 minutes ). Air should
have free access to the sample to maintain oxidizing conditions. Cool and
weigh the crucible to 0.1 mg and check the loss in weight by a second
heating for 5 minutes and reweighing after cooling.
5.3.2 The percentage loss on ignition nearest to 0.1 shall be calculated as
follows:
Loss on ignition, percent = +- x 100
where
A = loss in weight, and
B = weight of moisture free sample used.
Nol~ -The significance of the determination of loss on ignition will vary according
to the nawrc of the sample. The figure obtained may include loss due to the
oxidation of any carbonaceous matter and gain due to the oxidation of any fcrrour iron
present.
5.4Silica
5.4.1Fuse one gram of the air-dried, finely ground, sample with about
7 g of anhydrous sodium carbonate in a covered platinum crucible. Raise
the temperature slowly until frothing ceases, then complete the fusion at
1 000°C for 30 minutes, occasionally swirling the melt to ensure thorough
mixing. Quench the melt by immersing the bottom half of the hot crucible
in cold water, then place the crucible and lid in about 100 ml of hot water
contained in a platinum or porcelain evaporating basin. Cover the basin
with a clock glass and add a few drops of absolute alcohol. Then gradually
add 30 ml of hydrochloric acid ( sp gr I.16 ). Warm until the melt is com-
pletely disintegrated and remove the crucible and lid, washing them
thoroughly and scrubbing them with a rubber-tipped rod. Crush any lumps
remaining in the solution.
5.4.2 Evaporate the solution, obtained from the fusion, to dryness break-
ing up from time to time the crust that forms and hinder evaporation. When
the residue is completely dry, cover the basin with a clock glass and drench
the residue with about 20 ml of hydrochloric acid ( sp gr 1.16 ). Allow to
stand for a few minutes, then add about 75 ml of hot, water to dissolve the
salts. Digest on a steam-bath for 5 minutes, then filter through an ashless
filter paper ( No. 40 Whatman paper or equivalent ). Transfer the silica
to the filter with a jet of. hot water; it is necessary to scrub the basin. Wash
the residue five times with hot dilute hydrochloric acid ( one percent )
followed by hot water until it is free from chlorides. Reserve the residue
8
rsrl727-l!w
and paper for the subsequent ignition, and transfer the filtrate and washings
back to the evaporating basin.
5.43 Again evaporate completely to dryness, cover the basin with a
clock glass and bake in an air-oven for one hour at 11O’C. Allow to cool,
then drench the residue with about 20 ml of hydrochloric acid ( sp gr l-16).
Allow to stand for a few minutes, add about 75 ml of hot water and digest
for 5 minutes on a steam-bath. Filter through another ashless filter paper
( No. 40 Whatman paper or equivalent ) transferring the residue to the
filter with a jet of hot water and scrubbing the basin with a rubber-tipped
rod. Wash five times with hot dilute hydrochloric acid ( one percent ),
followed by hot water until the residue is free from chlorides. Reserve the
filtrate and washings for the determination of ferric oxide and alumina.
5.44 Place the two residues and papers, without drying, in a weighed
platinum crucible and heat cautiously to dry the residue and char the papers.
Then burn off the carbon and finally ignite at 1 100 to 1 200°C for 30
minutes and then to constant weight. Cool and weigh to obtain the weight
of impure silica.
5.4.5 Moisten the weighed residue with a few drops of dilute sulphuric
acid ( 50 percent ) and add about 10 ml of hydrofluoric acid. Evaporate
slowly to dryness on a sand-bath ( or under a suitable radiant heater ) in a
fume-hood. Ignite the dry residue at 1 050 to 1 100°C for five minutes, allow
the crucible to cool and weigh. Subtract the weight of this residue from the
weight of impure silica to obtain the amount of silica in the sample taken.
If the residue weighs more than 5 mg, repeat the treatment with hydrofluoric
and rulphuric acids to ensure that all the silica is removed.
NOTB - For routine analysis, treatment with hydrolluoric acid may be omitted.
5.4.5.1 To this amount of silica, add the amount of silica recovered

from the residue derived fom the combined precipitates of alumina and
faric oxide as indicated in 55.4 and 5.6.1.
5.4.6 Add O-5 g of sodium or potassium persulphate to the crucible and
treat below red heat until the small residue or impurities are dissolved in
the melt. Cool, dissolve the fused mass in water, add it to the filtrate and
washings reserved for the determination of the combined alumina and
ferric oxide.
5.5 Combined Ferric Oxide and Alumina
5.5.1 To the solution obtained in 5.4.6 ( approximately 300 ml ) add 2

to 3 g of solid ammonium chloride, warm the solution to about 80% and
add diluted ammonia solution ( 50 percent ) with stirring until preci-
pitation appears to be complete. Render the solution just alkaline to
methyl red. Roil the alkaline solution for two minutes, allow to stand for
9
five minutes for the precipitate to settle and filter through an ashlesa filter
paper ( No. 41 Whatman paper or equivalent ). Transfer the precipitate
to the filter and wash five times with hot faintly ammoniacal ammonium
nitrate solution ( one percent ). Reserve the i&ate and washings and
transfer the precipitate back to the precipitation beaker. Moisten the
paper with hot dilute hydrochloric acid ( 50 percent ) and wash thoroughly
with water adding these washings to the precipitation beaker. Reserve
the paper for ignition. Dissolve the residue in a slight excess of hydrochlo-
ric acid, add one gram solid ammonium chloride and dilute the solution
to about 300 ml with water. Repeat the precipitation as before and when
the precipitation is complete add some macerated filter-paper pulp or filter
accelerator and stir vigorously. Filter through another ashless filter paper
( No. 41 Whatman paper or equivalent ) and wash the precipitate free
from chlorides with hot faintly ammoniacal ammonium nitrate solution and
reserve the precipitate and paper for ignition.
5.5.2 Acidify the combined reserved filtrate with hydrochloric acid and
evaporate to about 150 ml. Make it just alkaline to methyl red with dilute
ammonia solution ( 50 percent ). Any precipitate should be filtered off,
reprecipitated, washed as before and reserved for ignition. Acidify the
solution or the filtrate’ and washings with hydrochloric acid and reserve for
the determination of lime and magnesia.
5.53 Place the precipitates and papers reserved for ignition in a weighed
platinum crucible and heat, slowly at first, to dry the precipitates and char
the papers. Burn off the carbon and finally ignite the residue at 1050 to
1 100°C to constant weight taking care to prevent reduction. The weight
of combined ferric oxide, alumina and titanium oxide ( together represented
as RsO, ) is thus obtained.
55.4 If silica is suspected to be carried into the filtrate used for this esti-
mation, proceed as follows:
Treat the residue in the crucible with a drop of water, about 5 ml
of hydrofluoric acid and a drop of sulphuric acid and evaporate
cautiously to dryness. Finally heat the crucible to 1 050 to 1 100%
for one or two minutes, cool and weigh. The difference between
this weight and the weight previously obtained represents the
amount of residue silica. Subtract this amount from the weight
of combined ferric oxide and alumina found in 5.5.3. Add the same
amount to the silica already determined in 5.4.5.
5.6 FerricOxide
5.6.1 A separate de termination of the f&c oxide is often not required
but where called for shall be done as follows:
I-&at the precipitate ( see Note below ) obtained in 5.551 with
fused potassium or sodium pyrosulphate until solution is complete.
10
Dissolve the fused materials in 50 ml of sulphuric acid ( 10 percent )
and evaporate to fumes. Cool, dilute with water, and filter off the
silica washing with hot water. Reserve the filtrate for the deter-
mination of ferric and titanium oxides. Ignite the silica in a
platinum crucible and weigh. Treat to precipitate with 5 ml of
hydrofluoric acid and 2 to 3 drops of sulphuric acid. Evaporate
to dryness, ignite and weigh. The loss in weight represents extra
silica which should be added to that determined previously in
5.4.5 and also deducted from the weight of the combined oxides,
R,O,, obtained in 5.5.3.
Ncrra - Instead of ‘&sing directly in the platinum crucible in which the RIO,, was
ignited, the precipitate may be brushed into a porcelain crucible and then fused with
potasaium or sodium pyrcsulphate. This avoids loss of platinum by the action of the
pyrcsulphate, and nq platinum ia present in the filtrate to interfere with the iron deter.
mination.
5.6.2 Evaporate the filtrate obtained in 5.6.1 to about 75 ml. Cool and
dilute to 100 ml in a volumetric flask. Add 25 ml of dilute hydrochloric
acid ( 50 percent ) and heat to boiling. Reduce the iron by adding stannous
chloride solution drop by drop from a pipette with constant swirling of the
beaker until the solution is colourless. Then add one drop in excess.
Cool quickly in running water, then add at one stroke 15 ml of saturated
mercuric chloride solution. Allow to stand for 3 minutes and then transfer
with the washing to a 1 000-ml beaker containing 300 ml of cold distilled
water and 25 ml of manganese sulphate solution. Titrate with standard
004 N potassium permaganate solution, added very slowly while stirring
constantly, until a permanent pink end point is obtained, and calculate the
amount of ferric oxide present.
5.7 Uunina - Subtract the weight of ferric oxide calculated as in 5.6.2
and the small amount of silica found in 5.6.1 from the total weight of oxides
found under 5.55. The remainder is the weight of alumina and of small
amounts of other oxides which may also be reported as alumina for purpose
of this analysis.
5.8 CaIeisun Osidt- To the filtrate from 5.5.1 reserved after determina-
tion of the combined ferric oxide and alumina, add one gram of ammonium
oxalate. Roil the solution, then add, with stirring, dilute ammonia solution
( 50 percent ) until the solution is alkaline, followed by an excess of 10 ml
ofdilute ammonia solution ( 50 percent 1. Cover the beaker with a clock
glass and digest on a water-bath for two hours. Allow to cool and stand,
preferably overnight, then filter through a filter paper ( No. 42 Whatman
paper or equivalent ) and wash the precipitate four times with cold
ammotium oxalate solution ( one percent ). Reserve the filtrate and wash-
ings for the dete rmination of magnesia.. Wash the precipitate back into the
precipitation beaker. Moisten the filter paper with hot dilute nitric acid
( 50 percent ) and dilute the solution to about 80 ml. Add about Q2 of
solid ammonium oxalate, boil the solution and precipitate the calcium oxa& te
11
IS : 1727 - 1967
as before. Allow to cool and stand for at least three hours. Filter through
a filter paper ( No. 42 Whatman paper or equivalent ) and wash the preci-
pitate thoroughly with cold ammonium oxalate solution ( one percent ).
Combine the filtrate and washing with the solution reserved for the magnesia
determination and acidify with hydrochloric acid.
5.8.1 Carefully ignite the precipitate and papers in a weighed platinum
crucible slowly at first, to burn off the carbon and finally at 1 100°C for
15 minutes. Allow to cool over a good desiccant as the ignited precipitate
is very hygroscopic. Weigh rapidly to obtain the weight of calcium oxide.
5.9 Magnesia - Acidify the filtrate set aside in 5.8 with hydrochloric acid
and concentrate to about 150 ml. Add to this solution about 10 ml of
ammonium hydrogen phosphate ( 150 g/l ) and cool the solution by placing
in a beaker of ice water. After cooling, add ammonium hydroxide drop by
drop while stirring constantly until the crystalline magnesium ammonium
phosphate begins to form, and then add the reagent in moderate excess
( 5 to 10 percent of the volume of the solution ), the stirring being continued
for several minutes. Set the solution aside for at least 16 hours in a cool
atmosphere and then filter using filter paper ( No. 42 Whatman paper or
equivalent ). Wash with ammonium nitrate wash solution. Place in a
weighed platinum crucible, slowly char the paper and carefully burn off the
resulting carbon. Ignite the precipitate at 1 lOO”C, to constant weight,
taking care to avoid bringing the pyrophosphate to melting. From the
weight of the magnesium pyrophosphate obtained, calculate the magnesia
content of the material taken for test.
5.10 Sulpharic Anhydride - To one gram of the sample add 25 ml of
cold water and, while the mixture is being stirred vigorously, add 5 ml of
hydrochloric acid. If necessary, beat the solution and grind the material
with the flattened end of a glass rod until it is evident that the decomposition
of the pozzolana is complete. Dilute the solution to 50 ml and digest for
15 minutes. Filter and wash the residue thoroughly with hot water. Set
aside the filter paper with the residue. Dilute the filtrate to 250 ml and heat
to boiling. Add slowly, drop by drop, 10 ml of hot barium chloride solution
and continue the boiling until the precipitate is well formed. Digest the
solution on a stcambath for four hours or preferably overnight. Filter the
precipitate with filter paper ( No. 42 Whatman paper or equivalent ), wash,
place the paper and contents in a weighed platinum or porcelain crucible,
and slowly incinerate the paper without inflaming. Then ignite at 800 to
909X, cool in a desiccator and weigh the barium sulphate. From the
weight of the barium sulphate obtained, calculate the sulphuric anhydride
content of the material taken for test.
.
5.11 Dete rmination of Soluble Salts - Weigh 25 g of the sample and
transfer to a 500~ml beaker. Add 100 ml of cold distilled water and stir the
contents frequently for three hours. Decant through a filter paper ( No. 42
Whatman paper or quivalent ) into a 500-ml graduated Ilask. Refilter the
12
Isrrm-l!m
filtrate, if necessary, Return the tilter paper to the beaker. Add 250 ml
of distilled water and continue the extraction for another 90 minutes. Filter
and wash the material on the filter paper three times with cold distilled water.
Add the filtrate and washings to the first filtrate in the 500-ml. flask and
make up to the mark using distilled water. Shake the flask well and pipette
out 200 ml to a weighed platinum dish ( or porcelain dish, glazed inside and
outside). Evaporate to dryness, and heat to constant weight at 105 to
110°C.
Calculate the percentage weight of the soluble salts as below:
Soluble salts, percent = 10 w
where
w = weight in grams of the dried material.
5.11.1 If the soluble salt content is more than 0.2 percent, analyse it further
for sulphates, chlorides and nitrate in accordance with the relevant standard
methods of chemical analysis.
5.12 Reproducibility of Resalts - Make blank determinations on the
reagents for each constituent of the pozzolana and apply corrections, where
necessary. In all cases, n&&e check determinations and repeat if satis-
factory checks are not obtained. The difference between check determina-
tions shall not exceed O-5 percent for silica and alumina and 0.2 percent
for the other constituents.
6. DETERMINATION OF FINENESS
6.0 The fineness of pozzolana shall be determined by the procedure given

in 6.1 or 6.2 or by both depending upon the requirements of the specification.
6.1 Determination of Sped& Sdace of Pozzolana

6.1.1 Stops - This method of test covers the procedure for determining
by Blaine air permeability apparatus, the fineness of pozzolana as represented
by the specific surface expressed as total surface area in square ccntimetres
per gram of material.
6.1s Applrratus
6.13.1 No&# of a@mttu -The Blaine air permeability apparatus
consists essentially of a means of drawing a definite quantity of air through a
prepared bed of definite porosity. The number and size of the pores in a
prepared bed of cement of definite porosity is a function of the size of the
particles and determines the rate of air flow through the bed. The apparatus,
E;traa$ in Fig. 1, shall consist specifically of the parts described in 6.14.2
. .
6.1.2.2 Permeabili&cdl - The permeability cell shall consist of a rigid
cylinder 12.7 f 1 mm in inside diameter, constructed of glass or non-corroding
13
IS t 1727- 1967
COUPLING TO FIT
BOTTOM OF CELL
FLAT 3mm WIDE
FILTER P*PER
COUPLING TO FIT
----
TOP OF MANOMGTER ) FE&>j m
PERFORATED METAL DISC

WITH 30 To 60.1 mm d
HOLES EQUALLY DiSTRltiTE
MANOMETER ENLARGED DETAIL OF CELL AND PLUNGER

All dimensions in millimctrcs.
FIG. 1 BWNE AIR PERMEABILITYAPPARATUS
metal. The top of the cell shall be at right angles to the principal axis of
the cell. The bottom of the cell shall form an airtight connection with the
top ofjhe manometer. A ledge 0.5 to 1 mm in width shall be an integral part
tif the cell or iirmly fixed in the cell 50 f 15 mm from the top of the cell for
support of the perforated metal disk.
6.1.2.3 Disk - The disk shall be constructed of non-corroding metal
and shall be 0.9 f 0.1 mm in tlpickness,perforated with 30 to 40 holes 1 mm
in diameter equally distributed over its area. The disk shall fit the inside
of the cell snugly.
14
Is:17279l!J67
6.1.2.4 Plungtr - The plunger shall fit into the cell with a clearance of
not more than 01 mm. The bottom of the plunger shall have sharp square
edges and shall be at right angles to the principal axis. An air vent shall
be provided either in the centre or on one side of the plunger. The top of
the plunger shall be provided with ‘a collar such that when the plunger is
placed in the cell and the collar brought in contact with the top of the cell,
the distance between the bottom of the plunger and the top of the perforated
disk shall be 15-O f 1.0 mm.
6.1.2.5 Filter jm@r - The filter paper shall be medium retentive
( corresponding to No. 40 Whatman ). The filter paper disks shall be
circular, with smooth edges, and shah have the same diameter as the inside
of the wall. (Filter paper disks that are too small may leave part of the sample
adhering to the inner wall of the cell above the top disk. When too large in
diameter, the disks have tendency to buckle and cause erratic results. )
6.11.6 iM,,r+& - The U-tube manometer shall be ,constructed
according to the design indicated in Fig. 1, using nominal 9 mm outside
diameter, standard-wall glass tubing. The top of one arm of the manometer
shall fbrm an airtight connection with the permeability cell. The mano-
meter arm connected to the permeability cell shall have a line etched around
the tube at 125 to 145 mm below the top of the side outlet and also others
at distances of 15, 70 and 110 mm above that line. A side outlet shall be
provided at 250 to 305 mm above the bottom of the manometer for use in
the evacuation of the manometer arm connected to the permeability cell.
A positive airtight valve or clamp shall be provided on the side outlet not
more than 50 mm Tom the manometer arm. The manometer shall be
mounted fumly and in such a manner that the arms are vertical.
6.1.2.7 Marwmcter liquid-The manometer shall be filled to the mid-
point with a nonvolatile, nonhygroscopic liquid of low viscosity and density,
such as dibutylphthalate ( dibutyl 1, 2benzenedicarboxylate ) or a light
grade of mineral oil.
6.1.2.8 Timer - The timer shall have a positive starting and stopping
echamsm and shall be capable of being read to the nearest 0.5 second or
%. The timer shall be accurate to @5 second or less for time intervals up to
60 seconds and to one percent or less for time intervals of 60 to 300 seconds.
6.19 CaMrarion of Appororur
6.1.3.1 Sam#~%-The calibration of the air permeability apparatus
shall be made using National Bureau of Standards Standard Sample
No. 114 or any other cement sample having specific surface equal to the
appropriate certificate value of NBS Standard Sample No. 114. The sample
shall be at room temperature when tested.
.
NOTE- In the hence of NE3 Standard Sample No. 114, sampler of Indian cementa
b8viq rpecificsurfice cquivdmt to NB!3 Standard SaunpleNo. 1i4 may be uaal; mxh
nmpla ma be obtainal from the ACC Central Rcaearcb station, Bamhy-m
Rad, P.O. Lgk IadustrialEstate, ( Tbuu ).
15
m11727-1967
6.1.3.2 Bulk volumeof compactedbed of powder - The bulk volume of the

compacted bed of powder shall be determined by the mercury displacement
method as follows:
Place two filter paper disks in the permeability cell, pressing
down the edges with a rod slightly smaller than the cell diameter
until the filter disks are flat on the perforated metal disk; then
fill tha cell with mercury, removing any air bubbles adhering to
the wall of the cell. Use tongs when handling the cell. If the
cell is made of material that will amalgamate with mercury, the
interior of the cell shall be protected by a very thin film of oil
just prior to adding the mercury. Level the mercury with the
top of the cell by pressing a small glass plate against the mercury
surface until the glass is flush with the surface of the mercury.
Check that no void or bubble exists between the mercury surface
and the glass plate.
Remove the mercury from the cell, weigh and record the
weight of mercury. Remove one of the filter disks from the cell.
Using a trial quantity of 2.80 g of cement ( seeNote 1 ) compress
the cement ( see Note 2 ) in accordance with 6.1.3.5, with one
filter disk above and one below the sample. Fill the space
remaining in the top of the cell with mercury, remove
entrapped air, and level off the top as before. Remove the
mercury from the cell, weigh aud record the weight of
mercury.
The bulk volume occupied by the cement shall be calculated
to the nearest 0905 cm” as follows:
yL= Wll- W&
. ..*...........(I)
I)
where
V = bulk volume of cement in cm’;
W* = grams of mercury required to fill cell, no cement being in
cell;
wb = grams of mercury required to fill the portion of the cell
not occupied by the prepared bed of cement in the cell;
and
D LI density of mercury at temperature of test in g/cm*
( see Table 1 ).
At least two determinations of bulk volume of cement shall be
made, using separate compactions for each determination. The
bulk volume value used for subsequent calculations shall be the
average of two values agreeing within plus or minus 0’005 ems.
The temperature in the vicinity of the cell shall be noted and
recorded at the beginning and end of determination.
16
IS8172711967
Non I- It ir not nccusary to use the standard sample for the bulk volume
determination.
NWX 2 -The prepared bed of cement shall be firm. If too loose or if the cement
cannot be compressed to the d&red volume, adjust the trial quantity of cement used.
TABLE 1 DENSFlY OF MERCURY, VlSCOSlTY OF AlR (IS) AND 4;

AT GWEN TEMPERKMJRE
( C&IUS6.1.3.2 )
ROOM DXNSITYOF v- OF
‘MXRCURY Am, PoLwd
=-T?- Ill=”
It,
16 13.56 0.000 178 8 0*013 37

18 13.55 OX@01798 0.013 41
20 13.55 OWI 180 8 0.013 44
22 13.54 OGOO1818 0.013 48
24 13.54 0.000 182 8 0.0 13 52
26 13.53 0.000 183 7 0.013 55
28 13.53 o*ooo 184 7 0.013 59
30 13.52 O.@O 185 7 0.013 62
32 13.52 o*OOo186 7 0.01366
34 13.51 OTJOO 187 6 0.013 69
*The density of the mercury shall be determined separately.
6.1.3.3 Prejaration of sample -The contents of a vial of the standard

cement sample shall he enclosed in a 125 gram jar and shaken vigorously for
2 minutes to fluff the cement and break up lumps or agglimerates.
6.1.3.4 Weight of sample -The weight of the standard sample used for
the calibration test shall be that required to produce a bed of cement having
a porosity of O-500 f 0905 and shall be calculated as follows:
W=pV(l-c) ................................................... ( 2 )
where
W = sample required in grams;
p = specific gravity of test sample ( for Portland cement, a
value of 3.15 shall be used ) ;
Y = bulk v&me of bed of cement in ems, as determined in
accordance with 6.1.3.2; and
e = desired porosity of bed of cement ( 0.500 f 0905 ).
6.135 Preparation of bed of ccmcnt - The perforated diik shall be seated
on the ledge in the permeability cell. A filter paper disk shall be placed on
the metal disk and the edges pressed down with a rod slightly smaller than the
17
Is:1727-1967
cell diameter. A quantity of cement determined in accordance with 6.1.3.4

and weighed to the nearest 0’001 g shall be placed in the cell. The side of the
cell shall be tapped lightly in order to level the bed of cement. A filter paper
disk shall be placed on top of the cement and the cement compressed with the
plunger until the plunger collar is in contact with the top of the cell. The
plunger,shall then be removed slowly. Use of fresh disks is required for each
determination.
6.1.3.6 Permeabili~ test - The permeability cell shall be attached to
the manometer tube, making certain that an airtight connection is obtained
( seeNote 1 ) and taking care not to jar or disturb the prepared bed of cement.
The air in the one arm of the manometer U-tube shall be slowly
evacuated until the liquid reaches the top mark, and the valve shall then be
closed tightly. The timer shall be started as the bottom of the meniscus of
the manometer liquid reaches the second ( next to the top ) mark and shall
be stopped as the bottom of meniscus of liquid reaches the third ( next
to the bottom ) mark. The time interval measured shall be noted and
recorded in seconds. The temperature of test shall be noted and recorded
in degrees centigrade.
In the calibration of the instrument, at least three determinations of
the time of flow shall be made on each of three separately prepared beds of
the standard sample ( see Note 2 ). The calibration shall be made by
the same operator who makes the fineness determination.
Non 1 - If a rubber stopper is used for the connection, it should be moistened with
water; if a standard-taper joint is used, a little stopcock grease should be applied. The
efficiency of the connection may be determined by inserting stopper at the top of the
cell attached to the manometer and then partially evacuating the one arm of the mano-
meter; then closing the valve. Any continuous drop in pressure indicatm a leak in the
system.
NOTE 2 - Tbc sample may be refluffed and reuxxl for preparation of the teat bed,
provided that it is kept dry and all tests are made within 4 hours of the opening
of the sample.
6.1.3.7 Re-calibration - The apparatus shall be re-calibrated ( SCG
Note )
at periodic intervals to check:
a) for possible wear on plunger or permeability cell,
b) if any loss in manometer fluid occtus, and
c) if a change is made in the type or quality of the filter paper used for
the test.
NoTE -It is suggested that a secondary sample be prepared and umd as a linenas
standard for the check determinations of the instrument between regular calibrations
with the standard cement sample.
6.1 A Procedure
6.1.4.1 Tempraturt of tht test sample - The pozzolana sample shall be at
room temperature when tested.
18
ISr1727-1967
6.1.41 S&e of test sam&?e- The weight of the pozzolana sample used for
the test shall be adjusted so that a firm, hard bed is produced in the cell by
compaction process.
6.1.4.3 Preparation of the bed of test sample - The test bed of pozzolana
sample shahbe prepared in accordance with the method described in 6.1.3.5.
6.1.4.4 Permeability test -The permeability test shall be made in
accordance with the method described in 6.1.3.6 except that only one time of
flow determination need be made on one prepared bed of pozzolana.
6.1.5 Cakulations - Calculation of specific surface values shall be made

according to the following formulae:
8s ............ ... .............. ...... (a)
P(l --4dqwT8
8 PI ( 1 --G,) l/&d&d/ .....
S= ..I......................
(4)
P (1 -8) dqdZd/,
where
S = specifk surface in cm2/g of the test sample;
s, = specific surface in cm’/g of the standard sample used in
calibration of the apparatus;
PI = specific gravity of standard sample used in calibration of
apparatus ( assumed to be 3.15 ) ;
e, = porosity of prepared bed of standard sample used in
calibration of apparatus;
e = porosity of prepared bed of test sample;
7 = measured time interval, in seconds, of manometer drop
for test sample;
P = specific gravity of test sample ( for Portland cement value
of 3.15 shall be used );
T, = measured time interval in seconds of -nometer drop for
standard sample used in calibration of the apparatus;
*, = viscosity of air in poises at the temperature of test of the
standard sample used in calibration of the apparatus; and
u k viscosity of air in poises at the temperature of test of the
test sample.
NATE 1 -Values for t/7;- aud t/T may be taken from Tables I aud 2
respectively.
NATE 2 -F+ation 3 shall. be used when tbe temperature of test and of the test
sample is within *3X of the temperature of calibration teat of the standard fineness
sample, and quation 4 shall be used if the temperature of tats is outside this range.
19
Istl727-1%7
TABLE 2 VALUES FOR POROSITY OF CEMENT BED

(C&u 6.1.5)
o-495 O-348
0.496 o-349
o-497 od50
O-498 Oa52
0.499 O-353
0400 0354
O?iOl 0-w
o-502 O-356
o-503 o-357
O-504 O-358
O-505 0459
O-506 O-360
O-507 o-361
0.508 O-362
o-509 OS3
o-510 O-364
O-525 0*380
O-526 O-381
O-527 O-383
O-528 o-384
o-529 O-385
0.530 o-386
o-531 o-387
o-532 o-388
O-533 &389
o-534 oa90
o-535 O-391
20
6.1.6 R&sts - A retest shall consist of two determinations made as
prescribed in 6.1.4 and 6.1.5, using a freshly prepared test bed of the sample
for each detqmination. Care shall be exercised in the preparation of the
test beds, and precautions shall be taken to ensure an airtight connection
between the permeability cell and the manometer arm. The fineness value
reported shall be the average of the values calculated from retest determi-
nations agreeing within 2 percent of each other.
NOTK-If tats are done at 8 other than @5, the actual rosity value shall be
reported a&n with finenas value, since it is known that the in xated value for fineness
ehangw with ht e decrease or increase ot’ the value of e.
6.2 Determhudon of Fineness by Sieving

62.1 Sco#c- This method of test covers the procedure for determining
the fineness of particles by a sieve analysis.
62.2 Ap~amtus- Following sieves conforming to IS : 460-1962* shall be
used:
3OOmicron IS Sieve For dry sieving
15O-micron IS Sieve For dry sieving
limicron IS Sieve For wet sieving
45micron IS Sieve For wet sieving
NOTE- Where the requirements in the individual specification for a pouolanic
material d&r from the proviaionr of this clauac, the former shall prevail.
6.2.3 P@amtion of Saqlu - A representative sample shall be taken iu

accordance with the sampling procedure given in the respective specilication
for the material, and shall be thoroughly mixed. The weight of the
representative sample shall not be less than 200 g. The sample for sieving
shall be prepared from the laboratory samples as described in IS : 1607-196Ot.
6.2.4 Drying Stig -The sample shall be passed successively through
3@0-micron IS Sieve and GO-micron IS Sieve, starting with the largest.
Sieving shall be done and the results reported in accordance with IS : X07-
196ot.
6.223 Wet Sting - Separate determinations’shall be made for the percent-
age of material passing 75micron IS Sieve and 45-micron IS Sieve by wet
sieving.
6.2.5.1 Place 100 g of the material over each of the two sieves. Wash
the material with a jet of water and keep it well agitated. The washing shall
continue till the washings appear no more turbid. Dry the sieve and the
residue in an oven. Brush the residue Corn the sieve after drying, and weigh
on a balance sensitiveto 01 percent of the weight of’the test sample. The
21
Is:1727-1987
percentage of mai;erial passing each sieve on wet sieving shal1 be reported to

the nearest 0.1 percent by weight of the test sample.
7. DETERMINATION OF SOUNDNESS
7.0 Either of the methods given in 7.1 and 7.2 may be used for determining
soundness of pozzolanic test mixtures.
7.1 6 Le Chatelier ’ Method- The test shall be done as specified in
IS : 4031-1968* Methcds of Physical Tests for HydraulicCement ’ except
that in place of cement, a mixture of pozzolana and cement in the propor-
tion 0.2 Jv: O-8 by weight, blended intimately shall be used:
where
Jv _ Specific gravity of pozzolana
- Specific gravity of cement
7.2 Autoclave Test -The test shall be done as specified inIS : 4031-
1968* except that a mixture of pozzolana and cement in the proportion as
indicated in 7.1 shall be used in place of cement.
7.2.1 When determining soundness by this method, not less than six
specimens shall be tested at a time for arriving at an average result.
8. DETERMINATION OF INITIAL AND FINAL SETTING TIME
8.1 The test for initial and final setting time of pozzolana with lime and
cement shall be done in accordance with the requirements of IS : 4031-
1968* except that a mixture of pozzolana and cement in the proportion as
indicated in 7.1 shall be used in place of cement for making the paste. The
determination of standard consistency shall also be carried out in
accordance with IS : 4031-1968* using the mixture of pozzolana and
cements in the proportion as indicated in 7.1 instead of cement for making
the paste.
9. DETERMINATION OF LIMEREACTIVITY
9.1 Scope - This method of test covers the procedure for determining the
reactivity of the pozzolanic material with hydrated lime, as represented by
compressive strength of standard mortar test cubes prepared and tested
under specific conditions.
9.2 Size and Number of Test Specimens
9.2.1 The tests specimen shall be 50-mm cubes.

*Methods of physical tests for hydraulic cement.
22
IS : 1727- 1967
9.2.2 Unless otherwise specified in the relevant specification for the

pozzolana, three or more specimens shall be made for each period of test
specified.
9.3 Apparatus
93.1 Cube Moulds - Moulds for the 50-mm cube specimens shall be of
metal not attacked by cement-pozzolana or lime-pozzolana mortar and there
shall be sufficient strength and stifbness to prevent spreadin.g and wrapping.
The moulds shall be rigidly constructed in such a manner as to facilitate the
removal of the moulded specimen without damage. The moulds shall be
machined so that when assembled ready for use the dimensions and internal
faces shall be accurate to the following limits:
The height of the moulds and the distance between the opposite
faces shall be 50 & O-1 mm for new moulds, and 50 f O-5 m for
moulds in use. The angle between adjacent interior faces an Anbet-
ween interior faces and top and bottom planes of the mould shall
be 90 & O-5, degrees. The interior faces of the moulds shall be
plane surfaces with a permissible variation of 0.02 mm for new
moulds and 0.05 mm for moulds in use. Each mould shall be
provided with a base plate having a plane surface machined to a
tolerance of O-1 mm and made of non-absorbent and non-corrodable
material. The base plate shall be of such dimensions as to support
the mould during the filling without leakage.
9.3.2 Mix&g Apparatus - This shall have components and accessories as
described in 9.3.2.1 to 9.3.2.4.
9.3.2.1 Mixer - The mixer shall be an electrically driven mechanical
mixer of the epicyclic type, which imparts both a planetary and a revolving
motion to the mixer paddle. The mixer shall have at least two speeds,
controlled by definite mechanical means. ( Rheostat adjustment of speed
shall not be acceptable. ) The first or slow speed shall revolve the paddle at
a rate of 140 f 5 rev/min, with a planetary motion of approximately 62
rcv/min. The second speed shall revolve the paddle at a rate of 285 f 10
rev/min, with a planetary motion of approximately 125 rev/min. The
electric motor shall have a power of about 150 W. The mixer shall be
capable of adjustment so that when the bowl is in the mixing position the
clearance between the lower end of the paddle and the bottom of the bowl
shall be approximately 2.5 mm but not less than the approximate diameter
of a grain of the standard sand ( see 3.3 ).
9.3.2.2 Paddle - The paddle shall be readily removable, made of stain-
less steel, and shall conform to the basic design shown in Fig. 2. The
dimensions of the paddle shall be such that when it is in the mixing position
the paddle outline conforms to the contour of the bowl used with the mixer,
and the clearance between corresponding points on the edge of the paddle
23
IS t 1727- 1967
All dimsions in milljmetre.

FIG. 2 PADDLE
and the side of the bowl in the position of closest approach shall be
approximately 4 mm but not less than O-85 mm.
$31.3 Mixing bowl - The mixing bowl shall be removable and shall
have.a nominal capacity of about six litres. It shall be of the general shape
24
Ist1727-1967
shown in Fig. 3. It shall comply with the limiting dimensions shown in

Fig. 2 and shall be made of stainless steel. The bowl shall be so equipped
that it will be positively held in the mixing apparatus in a fixed position
during the mixi?g procedure. It shall be provided with a lid made of non-
absorbing mate4 and not attacked by the pozzolanic mixture.
200 DIA 4
3% I
1
__ __ ____ -_____
I
----------------
t
E -SACK BOWL
PIN ASSV
&+_-d
All dimenaiona in millimctres.
FIG. 3 MIXING BOWL
9.3.2.4 Scrapn - The scraper shall consist of a semi-rigid rubber blade

attached to a handle about 150 mm long. The blade shall be about 75 mm
long, 50 mm wide, and tapered to a thin edge about 1.5 mm thick.
93.3 FLOW Tab& and Acce.wric~ - The flow table and accessories shall
conform to the requirements given in IS : 5512-1969*.
*Flow table for use in tests of hydraulic cement and pozzolanic materials.
25
Is:1727-1967
93.4 Tamping Rod - The tamping rod shall be made of a non-absorptive,

non-abrasive, non-brittle material, such as a rubber compound having a
Shore A durometer hardness of 80 f 10 or seasoned teak wood rendered
non-absorptive by immersion for 15 minutes in paraffin at approximately
2OO”C, and shall have a cross-section of 12 x 25 mm and a convenient
length ( 125 x 150 mm ). The tamping face shall be flat and at right
angles to the length of the tamping rod.
9.3.5 Troroel- This shall have a steel blade 100 to 150 mm in length
with straight edge.
9.4 Preparation of MouIds - The interior faces of the specimen moulds
shall be thinly covered with mineral oil or light cup grease. After assembling
the moulds, excessive oil or grease shall be removed from the interior faces
and the top and bottom surfaces of each mould. Moulds shall then be set
on plane, non-absorbent base plates that have been thinly coated with mineral
oil, or light cup grease.
9.5 Preparation of Mortar

9.5.1 Clean appliances shall be used for mixing. The temperature of the
water and that of the test room at the time when the mixing operation is
being performed shall be from 27 f 2°C ( see IS : 196-1966: ).
9.5.2 The dry materials of the standard test mortar shall be lime:
pozzolana : standard sand in proportion 1: 2iU: 9 by weight blended
intimately:
where
Specific gravity of pozzolana
M=
Specific gravity of lime
The amount of water for gauging shall be equal to that required
to give a flow of 70 f 5 percent with 10 drops in 6 seconds as
determined in 9.5.3.
9.5.2.1 The following quantities of materials are suggested for prepa-
ration of mortar:
150 g Hydrated lime
300 x Mg Pozzolana
1350 g Standard sand
These quantities will suffice for preparing six test specimens
according to 9.6.
9.5.3 Determination of Flow

9.5.3.1 Trial mixing - With dry material as specified in 9.5.2 make
trial mortars with different percentages of water until specified flow is
*Specification for atmospheric conditiotu for testing ( f&d).
26
IS : 1727- 1967
obtained. Make each trial with fresh mortar. The mixing shall be done
mechanically by means of mixing apparatus as’ described in 9.9.2. Place the
dry paddle and the dry bowl in the mixing position in the mixer. Then
introduce the materials for batch into the bowl and mix in the following.
manner:
a) Place all the mixing water in the bowi.
b) Add the pozzolanic mixture to the water, then start the mixer and
mix at the slow speed ( 149 f 5 rev/min ) for 30 seconds.
c) Add the entire quantity of sand slowly over a period of 30 seconds,
while mixing at slow speed.
d) Stop the mixer, change to medium speed ( 285 f 10 rev/min ),
and mix for 30 seconds.
e) Stop the mixer, and let the mortar stand for one and a half minutes.
During the first 15 seconds of this interval, quickly scrape down into
the batch any mortar that may have collected on the side of the bowl,
then for the remainder of this iuterval, cover the bowl with the lid.
f) Finish by mixing for one minute at medium speed ( 285 f 10
rev jmin ) .
g) In any case requiring a remixing interval, any mortar adhering to
the side of the bowl shall be quickly scraped down into a batch with
the scraper prior to remixing.
Upon the completion of mixing the mixing paddle shall be
shaken to remove excess mortar into the mixing bowl.
9.5.3.2 Carefully wipe the flow-table top clean and dry and place the
mould at the centre. Place a layer of mortar mixed in accordance
with 9.5.3.1 about 25 mm in thickness in the mould and tamp 20 times with
the tamping rod. The tamping pressure shall be first sufficient to ensure
uniform filling of the mould. Then fill the mould with mortar and tamp as
specified for the first layer. Cut off the mortar to a plane surface flush with
the top of the mould by drawing the straight edge of a trowel ( held nearly
perpendicular to the mould ) with a sawing motion across the top of the
mould. Wipe the table top clean and dry, particularly taking care to remove
any water from around the edge of the flow mould. Lift the mould away
from the mortar one minute after completing the mixing operation. Im-
mediately drop the table through a height of 12.5 mm, ten times in six
seconds.
The flow is the resulting increase in average base diameter of the
mortar mass, measured on at least four diameters at approximately equi-
spaced intervals expressed as a percentage of the original base diameter.
9.5.4 The materials for each batch of moulds shall be mixed separately
using the quantities of dry materials, conforming to the proportions specified
in 9.!%2 and the quantity of water as determined in 9.5.3. Mixing of mortar
shall be done mechanically as described in 933.1.
27
ISr1727-1967
9.6 MonIding Test Specimens - Immediately following the preparation

of the mortar in accordance with 9.5.4 place the mortar in a 50-mm cube
mould in a layer of about 25 mm thickness and tamp 25 times with the
tamping rod. The tamping shall be just sufficient to ensure uniform filling
of the mould. Then fill the mould to overflow and tamp as specified for the
first layer. On the completion of the tamping, the tops of all cubes shall
extend slightly above the tops of the moulds. Cut off thc.mortar to a plane
surface flush with the top of the mould by drawing the straight edge
of a trowel ( held nearly perpendicular to the mould ) with a sawing motion
across the top of the mould.
9.7 Storage and Curing of Specimens - Cover the surface of the spe-
cimen in the mould with a smooth and greased glass plate. Keep the spe-
cimens with the moulds along with the cover plates under wet gunny bags
for 48 hours. Then remove the specimens from the moulds and cure at
90 to 100 percent relative humidity at 50 f2”C for a period of eight days.
Samples shall not be cured under water.
NOTE-This may be achieved by keeping the specimens in a one litrc capacity wide
mouth jar with screwed lid over a galvanized iron sheet platform placed at the bottom
of the jar. The platform is covered with a piece of paper. Water is kept to a depth of
about IO mm at the bottom? below the level of the platform. After placing the spcci-
men and fitting the lid, thc~ar is scaled with insulation tape and kept in an incubt~
adjusted for 50 f PC for eight days.
9.8 Procedure of Test -Remove the specimens after curing for eight
days in the incubator as described above and test for compressive strength
after they reach the room temperature. Test not less than three cubes.
The cubes shall be tested on their sides without any packing between the
cube and steel platens on the testing machine. One of the platens-shall be
carried on a hall and shall be self-adjusting, and the load shall be steadily
and uniformly applied, starting from zero and at a rate of 35 kgfcma/min.
9.9 GaIeuIation -Calculate the compressive strength from the crushing
load and the average area over which the load is applied. Express the result
nearest to 1 kg/cm*.
9.10 FauIty Cubes and Retests - Cubes that are manifestly faulty or
that give strengths differing by more than 15 percent from the average value
of all’test specimens, made from the same sample and tested at the same
period, shall not be considered in determining the compressive strength.
After discarding such cubes, if less than two strength test values are left for
determining the compressive stength at any given period, a retest shall be
made.
10. DETZRMINATION OF COMPRZSSIVE STRZNGTH OF

PO Z ZOLANA-CEMENT .MORTAR
10.1 Scope- Thii method of test covers the procedure for determining the
compressive strength of pozzolana mortar as obtained in standard mortar
test cubes prepared and tested under specified conditions.
28
Isr1727-1967
102 size of spedmens -The test specimens shall be 50 mm cubes.

10.3 Apparatus-The cube moulds, mixing apparatus, flow table, tamping
rod and trowel shall be the same as specified in 9.9.
10.4 Preparation of Moulds - The moulds shall be prepared in the same
manner as described in 9.4.
105 Preparation of Mortar

103.1 Clean appliances shall be used for mixing and the temperature
of the water and that of the test room at the time when the mixing operation
is being performed shall be 27 f 2°C ( see IS : 196-1966* ).
105.2 The dry materials for the standard test mortar shall be pozzolana :
cement : standard sand in proportion @2 N: O-8 : 3 by weight, blended
intimately,
where
.N=
Specific gravity of cement
The amount of water for gauging shall be equal to that required to
give a flow of 105 f 5 percent with 25 drops in 15 seconds as determined
in 9LL3.
105.2.1 The following quantities of materials are suggested for prepara-
tion of the mortar:
1OOxJvg Pozzolana
4QOg Cement
1500 g Standard sand
These quantities will suffice for preparing six test specimens accord-
ing to 10.6.
105.3 The materials for each batch of mot&b shall be mixed separately
using the quantities of dry materials, conforming to the proportions given
in 103.2 and the quantity of water as determined in accordance with the
procedure given in 9.!53 to give a %ow of 105 f 5 percent with 25 drops in
15 seconds. Mixing of mortar shall be done mechanically as described
in 953.1.
10.6 Moalding Test Spedmens - Immediately after mixing the mortar
in accordance with 9J.9, place the mortar in 50-mm cube moulds and
prepare test cubes in accordance with the method as given under 9.6.
10.7 Storage and Curing of S~acimena - Keep the cubes at a tempera-
ture of 27 f 2°C in an atmosphere of at least 90 percent relative humidity
rspccz~tion for rtnlorpheric coaditionrfor tatiag ( fa/f#$).
29
I8 : 1727- 1967
for 24 hours after completion of compaction. At the end of that period,

remove them from the moulds and immediately submerge in clean fresh
water and keep there until taken out just prior to breaking. The water
in which the cubes are submerged shall be renewed every seventh
day and shall be maintained at a temperature of 27 & 2°C. After they
have been taken out and until they are broken, the cubes shall not be allowed
to become dry.
10.8 Procedure of Test
10.8.1 Test not less than three cubes for compressive strength for each
of the periods of 7, 28 and 90 days, the periods being reckoned from the
completion of compaction. The compressive strength shall be the average
of the strengths of the three cubes for each period respectively.
10.8.2 The cubes shall be tested on their sides without any packing
between the cube and the steel platens of the testing machine. One of the
platens shall be carried on a base and shall be self-adjusting, and the load shall
be steadily and uniformly applied, starting from zero at a rate of
140 kg/cms/min.
10.9 Calculation - Calculate the compressive strength from the crushing
load and the average area over which the load is applied. Express the
result nearest to 1 kgjcms.
10.10 Faulty Cubes and Retests - Cubes that are manifestly faulty or
that give strengths difTermg by more than 15 percent from the average value
of all test specimens, made from the same sample and tested at the same
period, shall not be considered in determining the compressive strength.
After discarding such cubes, if less than two strength test values are left for
determining the compressive strength at any given period, a retest shall
be made.
10.11 CorresFonding Test on Plain CementsIurd Mortar Cubes -
For the purpose of comparison, similar tests with cubes from mortar con-
taining no pozzolana shall be carried out as follows:
Not less than three mortar cubes shall be prepared out of a mix
with one part of ordinary Portland cement used in this test and three
parts of standard sand, stored and tested in the same manner. as
described in 10.5 to 10.9 and their average strength calculated.
11. DETERMINATION OF TRANSVER!3E STRENGTH OF THE

PO Z ZOLANA-CEMFNr MORTAR
11.1 8cope -This method of test covers the procedure for determining
the transverse strength of the pozzolana mortars as obtained on standard
rectangular specimens prqared and tested under ape&led conditions.
IS : 1727- 1967
11.2 Apparatus
11.2.1 Miring Apflaratus - The mixing apparatus shall be same as
specified in 9.3.2.
11.2.2 Joltang A@aratus -A typical design of the jolting apparatus is
shown in Fig. 4. The apparatus shall consist essentially of a rectangular
table rigidly connected by two light arms to a spindle at a horizontal distance
of 800 mm from the centre of the table. The table shall incorporate on its
lower face a projecting lug with a plane face, beneath which is a small stop
with a rounded upper surface. When the projecting lug rests on the stop,
its plane face and that of the table shall be horizontal. There shall be pro-
vided a cam made of hard or case-hardened steel, by means of which the
table can be raised and then allowed to fall freely from a height of 15 mm
before the lug strikes the stop.
11.2.2.1 The cam shall be driven by means of an electric motor of about
250 W and a reduction gear at a speed of one revolution per second. It is
recommended that the motor be provided with a device which automatically
stops it after 60 jolts.
11.2.2.2 There shall be arrangements to place the mould shell on the
table,in such a way that the length of the three compartments is perpendicular
to the axis of rotation of the cam. The mould shall be located on the table
with the aid of suitable reference marks, so that the centre of the central
compartment is directly above the point of percussion. The mould sur-
mounted by its hopper shall be clamped rigidly to the table, for example, by
means of wing nuts.
11.2.2.3 The combined weight of the table, mould, hopper and clamps
shall be 20 f 1 kg.
11.2.2.4 The apparatus shall be fixed on a concrete base 1 000 x 300
mm and 800 mm high. The base plates of the two frames carrying the cam
and the spindle about which the table rotates shall each be fixed to the
concrete base by means of four anchor bolts, and when fixing them,
a thin layer of rich mortar shall be placed between the base plates
and the concrete base in order to ensure perfect contact.
11.2.2.5 To reduce noise, the concrete base shall be placed on four-
rubber pads of suitable size. The table shall be horizontal when at rest,
and the common normal through the point of contact of the lug and stop
shall be vertical. The lug striking face and the stop shall be replaced as
soon as the above condition is no longer met. Ball bearings shall be em-
ployed for the spindles about which the table and the cam rotate. If plain
bearings are used, the play of the spindles in them shall not exceed 0.1 mm.
11.2.3 Moda3 - The moulds shall be made of hard steel not readily
attacked by the pozzolana mortar and shall embody three compartments
31
. 800 - &-IO04
AU dimensiona in miUimetra,
FIG. 4 JOLTING APPNUTUS
IS : 1727 - 1967
permitting the preparation of three specimens at a time. The internal

dimension of each compartment, when assembled ready for use, shall be:
Length 160 f O-4 mm
Width 40 f O-1 mm
Height 40 f O-1 mm
11.2.3.1 The mould walls shall be at least 10 mm thick, the internal
opposite faces of 40 x 160 mm shall be plane to within 0.02 mm and the
angle between the base and the mould shall be 90 f WY.
11.2.3.2 The mould shall rest on a machined steel base plate to which it
shall be securely clamped. The mould shall be rigidly constructed but in
such a manner as to facilitate the removal of the moulded specimen
without damage. The base plate shall accurately fit the mould to prevent
any leakage during filling and the parts of the mould when assembled
shall be ensured by suitable methods to be positively held together both
during the filling and subsequent removal of the filled mould from the jolting
apparatus, in order to prevent any damage to the moulded specimen.
11.233 Each compartment shall, in turn, be surmounted by a hopper
made of steel or non-ferrous metal, with vertical walls 20 to 40 mm in height.
During filling, the interior vertical surfaces of the hopper shall be within
those of the compartment by a distance not exceeding 0.4 mm.
11.2.4 Apparatus of Transverse Test - The apparatus for testing transverse
strength shall consist of two supports in the form of rollers 10 mm in diameter
and spaced 100 mm apart, where the test prism is placed centrally with one
of its faces resting on them, and of a third roller of the same diameter equi-
distant from the first two and transmitting the applied load to the opposite
face of the prism. One of the supporting rollers shall be self-aligning. The
apparatus shall be fixed on to a testing machine which is capable of applying
and measuring small loads ( less than 1.00 kg ) with an accuracy of one per-
cent in the upper four-fifths of its range.

11.3.1 The specimens shall be in the form of a rectangular bar of dimen-
sions 160 x 40 x 40 mm.
11.3.2 Unless otherwise specified in the relevant specification for the
specified.
11.4 Preparation of Moulds - In assembling the moulds ready for use,
cover the joints between the parts of the mould with a thin film of petroleum
jelly and apply a similar coating of petroleum jelly between the contact
surfaces of the bottom of the mould and its base plate in order to ensure that
no water escapes during vibration. Treat the interior faces of the mould
with a thin coating of mould oil.
33
11.4.1 The mould and its hopper shall be fixed securely on the table of
the jolting apparatus by means of the clamp.
11.5 Prepmration of Mortar
11.5.1 Clean appliances shall be used for mixing and the temperature of
the water and that of the test room at the time when the mixing operation
is being performed shall be 27 f 2°C.
11.5.2 The dry materials of the standard test mortar shall be pozzolana,:
cement: standard sand in proportion 0.2 IV: 0.8: 3 by weight, blended
intimately:
where
N = Specific gravity of pozzolana
The weight of water shall be equal to half the weight of pozzolana
plus cement in the above mixture.
using the quantities of materials, conforming to the proportions given
in 11.55. Mixing of mortar shall be done mechanically as described
in 953.1.
11.6 Moulding Test Specimens - After Iixing the mould and its hopper
on the jolting table, introduce directly from the mixer the first layer of mortar
of about 320 g into each of the moulding compartment ( for example, by
using a spoon of known capacity). Spread this layer by means of a steel
plate levelling tool which is to be drawn twice forward and backward along
the mould while pressing its flanges against the top of the hopper. Give
66 jolts to the frrst mortar layer in 60 seconds. Then introduce a second
identical layer of mortar, level and compact as before. Lift the mould from
the jolting table and remove its hopper. Strike off the excessive mortar
with a metal straight edge held nearly vertical and moved slowly along the
length of the mould with a transverse sawing motion. Then smooth lightly
the surface, using the straight edge held almost flat.
11.7 Storage and Curing of Specimens -After completion of the jolt-
ing, cover the specimens in the mould by steel or rubber sheet and keep them
at a temperature of 27 f 2°C in an atmosphere of at least 90 percent rela-
tive humidity for 24 hours. At the end of that period, remove them from the
mould with due precautions, preferably with the apparatus shown in
Fig. 5. Immediately keep them submerged, preferably standing on end, in
saturated still water until the time for testing. The specimens shall be kept
apat from each other allowing free access of water to all their faces.
11.7.1 The volume of curing water shall be at least four times that of the
test specimens. Half the curing water shall be replaced every lifteenth day.
34
I+
421
6--(
All dimcnsiau in miuilnetra.

FIO. 5 &‘PAIuTUS FOR I)EMOULDmO
35
Is : 1727 - 1967
The temperature of curing water shall be maintained at 27 f 2%. The

specimens shall be taken from the water only less than 15 minutes before test.
In order to satisfy this condition, they shall be transported to the test machine
in a container full of water. They shall then be wiped with a clean cloth SO
that any deposit that might have accumulated on them is removed. The
specimens shall not be allowed to become dry until they are tested.
11.8 Procedure of Test -Test not less than three specimens for trans-
verse strength in the apparatus described in 11.2.4 for each of the periods of
7,28 and 90 days, the period being reckoned from the completion of jolting.
The load shall be progressively increased during application at the rate of
5 f 1 kg/set. The transverse strength shall be the average of the strengths
of the three specimens for each period respectively.
11.9 Calcalation - The transverse strength of the specimen ‘I, shall be
calculated by the formula:
T = 0.234 P
where
P = applied load in kg at the time of breaking.
The value of T shall be expressed nearest to 1 kg/cm2.
11.10 Faulty Specimens and Retests -Specimens that are manifestly
faulty or that give strengths differing by more than 15 percent from the
average value of all test specimens, made from the same sample and tested
at the same period shall not be considered in determining the transverse
strength. After so discarding, if less than three values are left for deter-
mining the transverse strength at any given period, a retest shall be made.
12. DETERMINATION OF DRYING SHRINKAGE IN

PO Z ZOLANA-CEMENT MORTAR
12.1 Scope - This method of test covers the procedure for determining the
drying shrinkage of pozzolana-cement mortar as obtained on rectangular
specimens prepared and tested under specified conditions.
12.2 Apparatis
12.2.1 &&-The scales shall conform to the following requirements:
On scales in use the permissible variation at a load of 1 000 g shall be
f 1.0 g. The permissible variation on new scales shall be one-half of thii
value. The sensibility reciprocal shall be not greater than twice the
permissible variation.
12.2.2 Weights - The permissible variations on weights in use in weighing
the cement shall be as prescribed in Table 3.
36
ISt1727-1967
TABUS -IS VARIATIONS ON WE3GElTS

( CCCRW
12.2.2 )
WBlOIiP PgRYIgllBLE WRfOHT PaRxrnIllLN
VARlATlON ON vNUAT3ONON
WlUOEiT!J IN USE, wEmiTs IN USE,
PLUS OR MINUS PLUS OR &iIRUS
8 g
500 0.35
300 0.30
250 0.25
200 o-20
100 o-15
50 0.10
123.3 Trowel- This shall have a steel blade 100 to 150 mm in length
with straight edges.
12.2.4 Length Comparator - Changes 3 length of the test specimen shall be
measured by a dial gauge or micrometer comparator having a range of at
least 7.6 mm. The instrument shall be graduated to at least O-025 mm and,
when tested at any point throughout its range, the error shall be not greater
than fO*050 mm. The difference between repeated measurements shall be
not greater than O-025 mm. The comparator shall be equipped with a steel
reference bar having an insulating grip and shall be frequently checked with
this reference bar.
12.2.5 Flow Table - Components, accessories ( including mould ),
mounting and lubrication of flow table shall conform to IS : 5512-1969*

12.3.1 The test specimens shall be in the form of rectangular bars
25 x 25 mm in section and 250 mm long.
123.2 Unless otherwise specified in the relevant specification for the
specified.
12.4 Preparation of Moulds -The moulds shall be thinly covered with
mineral oil; after this operation the stainless steel or non-corroding metal
reference points shall be set, care being taken to keep them clean and free of
oil.
12b5 Preparation of Mortar
12.5.1 Clean appliances shall be used for mixing, and the temperature of
the water and that of the test room at the time when the mixing operations
is being performed shall be 27 &2X,
*Flow table for use in tati of hydraulic cement and pozzolanic mate&&
37
fs:l727-1967
1252 The dry materials for the standard test mortar shall be pozzolana :
cement : standard sand in proportion 0*2N: O-8 : 3 by weight, blended
intimately:
where
N=
The amount of water for gauging shall be equal to that required to
give a flow between 100 and 115 percent with 25 drops in 15 seconds, as
determined in 9.53.
12.5.2.1 The following quantities of materials are suggested for pre-
paration of the mortar:
6OxNg Pozzolana
24Og Cement
9OOg Standard sand
in 12.5.2 and the quantity of water as determined in accordance with the
Procedure given in 9.5.3 to give a flow of 100 to 115 percent with 25 drops
m 15 seconds. Mixing shall be done mechanically as described in 96.3.1.
12.6 Moulding Specimens - Immediately following the completion of
mixing, the test specimen shall be moulded in two layers, each layer being
compacted with the thumbs and forefingers by pressing the mortar into the
comers, around the reference inserts and along the surfaces of the moulds
until a homogeneous specimen is obtained. After the top layer has been
compacted, the mortar shall be levelled off flush with the top of the mould
and the surface smoothed with a few strokes of the trowel. During the
operations of mixing and moulding, the hands shall be protected by rubber
gloves.
12.7 Roetdura of Test

12.7.1 After filling the moulds, place them immediately in a moist room or
moist closet for 24 f 2 hours. Then remove the specimens from the moulds
and immediately immerse in water at 27 f 2°C and allow @em to remain
there for six days.
12.7.2 Remove the specimens from the water and measure for length
using a length comparator. Protect specimens against loss of moisture prior
to reading for initial length. The temperature of the test specimens at
the time of initial measurement shall be 27 f,2“C. Store the specimens
in a closet or room maintained at 27 f 2°C and 50 f 5 percent rclatk
humidity. Measure the length of the specimens again 28 days after the
initial measurement. Place the specimens in the comparator with the same
38
ls,17!27-I%7
end uppermost with respect to the position of the specimens as when the
initial measurement was made. When making the measurements, the
specimens, comparator, and the reference bar shall be at a temperature
of 27 f 2°C.
12.3 C&ulatios~ ‘- After the specimens are measured as in 12.7.2 at the

age of 7 and 35 days, calculate the average di&rence in length of the three
specimens to the nearest O-01 percent of the efktive gauge length, and
report this difference as the drying shrinkage.
13. DETRRMINATION OF THE PRRMRARILITYOFTHE

POZZOLANA-CEMENT MORTAR
13.1 - This method of test covers the procedure for determining khe
3Yo ‘ty to water of the pozzolana mortar prepared and cured under
permeab
specified conditions, by measuring the percolation of water through standard
cylindrical specimens.
13.2.1 Pcrmcability Unit - The permeability unit S&II consist of a speci-

men container ring of 100 mm diameter and 50 mm high, held between a
bottom plate and a water cell. The hydraulic head for testing shall be
obtained by connecting the unit to a compressor through a water pressure
vessel. A pressure regalator and pressure gauge shall be included between
the compressor and the water pressure vessel to indicate the test pressure.
Water percolating through the specimen shah be collected in a container.
Typical details of an individual unit are given in Fig. 6 and 7. The water
cell shall be 100 mm diameter brass cylinder and the top and bottom plates
shall be either of brass or any other non-corroding metal. The connecting
pipeline from the water cell to the water pressure vessel shall also be of non-
corroding metal or of hard board polythene. This requirement is necesssary
since the tests last over a number of days in which mild steel or simiIar ma-
terials will get corroded and the rust formed will coat the top of the speci-
mens and affect the permeability. The connection of units to the air cylinder
shall be done with armoured healy-duty rubber hose.
13.2.2 Rammer-A rammer of the type shown in Fig. 8 shall be used to

compact the mortar. The rammer shall consist of a plunger weighing
500 f5 g which shall fall freely through a height of 150 f 1 mm in a tubular
guide. The base of the plunger shall have a diameter of 50 f 1 mm.
133 l@tasi&
133.1 The dry materials for the standard test mortar shall be pozzolona :
39
CONNECTION TO
WASHER I AIR CYLINDER
z- z
T-L/
120
RUBBER
WASHER
-&0r,
t
-
,
I
100 g-
11:
#-
2Bp
‘\
1 LWATER
WATER
INLET
CELL
t- I
RUBBEi
WASHER
I
SO
3 SPECIMEN CAST
IN THE CYLINDER
BOTTOM PLATE
% ‘p
LWATER OUTLET
SECTION XX
All dimensions in mihnetres.
FIG. 6 DETAILS OF PERMEABILITYUNIT
40
BBER PIPE
ASS OR POLVTIENE PIPE
4rs STAN0 FORAPmRAllls

CONTAINER
wml? PRESSURE VESSEL
SECTION xx
MAX PRESSURE ‘III+
FIG. 7 GENERAL
&mANQEMENT OF PERMRABILJTY TESTUNIT
AMMER
TUBULAR GUIDE
RUBBER GASKET
All cliaumiona in miuimetm.

Fro. 8 SPECIMENCOMPACTINGAPPARATUS
cement : sand in proportion 0*2X: 0.8 : 5 by weight, blended intimately,

where
Specific .gravity of pozzolana
N=
133.2 The amount of water for gauging shall be qual to that required to
give a flow of 105 f 5 percent with 25 drc~psin 15 seconds as determined
in 95.3.
13.33 sarnd - The sand to bc used in the preparation of mortar for this
test shall be natural, rounded siliceous sand with a maximum possible amouht
of quartz, The sand shall preferably be -obtained Corn EnnoPe. The
42
IStl727-1%;
particle size di&ibution, &tmmined by sieving, shall be between the linn~

given below:
SiCZht Cumulative Ibtaitwd ( Percent )
290-mm IS Sieve 0
1.7~mm IS Sieve 5f5
190-mm IS Sieve 33 f 5
500 micron IS Sieve 67 f 5
150micron IS Sieve 88 f 5
75 micron IS Sieve 98 & 2
13.4 Preparation of Mortar

13.4.1 Cltan appliances shall be used for mixing, and the temperature
of the water and that of the test room at the time when the mixing operation
is being performed shall be 27 f 2°C.
in 13.3.1 and the quantity of water as determined in accordance with the
procedure given in 9.5.3 to give a flow of 105 f 5 percent with 25 drops in
15 seconds. Mixing shall be done mechanically as described in 9.5.3.1.
13.5 Preparation of Speiimens -The container ring shall be given a

thin coating of neat cement slurry and the mortar shall be placed in it in
two layers. Each layer shall be compacted with 10 blows of the rammer
described in 13.2.2, falling freely through a height of 150 f 1 mm in its
tubular guide. During compaction the guide of the rammer shall remain
in contact with the wall of the container ring. It shall ‘be moved through a
uniform distance after each blow so as to cover the entire periphery of the
container ring after 10 blows. After compaction the top of the specimen
shall be levelled off with a 12 mm diameter rod slowly and firmly moved over
the surface. No trowel@ or other type of surface finiih shall be allowed
13.6 Cssring pnd srrSpoB6pr&mens - Keep the container ring with

the specimens at a tern- of 27 f 2°C in an atmo@here of at least
90 percent relative huoridity for 24 hours. At the end of that period, sub-
merge the specimens in clean fresh water and keep there for 27 days, and
take it out just prior to testing. The water in which the specimens are sub-
merged shall be renewed every seventh day and shall be maintained at a
temperature of 27 f 2%.
13.7 Roc&sre at Teat-The spccimcnsshall then be fitted into the

testing apparatus as shown in Fig. 6. Water shall be poured into the water
cell till it is nearly filled. The water inlet shall than be closed with the lid
screwed tight.
43
lstl727-1967
An initial pressure of about @5 kg/cm’ shall be applied to the

water and from time to time the collecting container shall be taken out and
weighed to determine the rate of percolation. The rate of percolation will
be comparatively high in the initial stages and will then become stabilised.
At this stage the pressure shall be increased again by 0.5 kg/ems and this
procedure repeated until a final pressure of 2 kg/cm’ is reached. When a
stable flow has been reached at this pressure readings of the percolation shall
be taken at fixed intervals of time for 8 hours.
The test shall bc carried out at a temperature of 27 f 2°C. For each
test three specimens shall be tested at a time.
131 c8lculation -The coefficient of permeability shall be calculated
from the formulaz
where
K = coefficient of permeability in cm/xc/unit gradient,
Q = quantity of water collected in g,
J= thickness of the specimens, in cm,
w= density of water in g/cm* normally equal to one,
a= area of cross-section of the specimen in cm*,
T = time of collection in seconds, and
h = net pressure head on the specimen in cm of water.
The average for three specimens shall be reported as the permeability
oftheprorb=
l&9 Fdty SpedlwM ad Retests -Specimens that are manifatly
faulty or that give permeability values differing by more than 15 percent
from the average shall not be considered. In such cases, a retest shall be
made.
14. REDucTloIu IN BANDSILICARELEASEEY

POZZOLANA
14.1 Sup- These tests will help to find out the efhxtiveness of a few
pozzolanas in reducing the harmful effects of alkali-aggregate reaction in
concrete. However, the tests are not applicable to all types of pozzolana.
141 A-
143.1 Rhn&on conta&s - These shall be of 50 to 75 ml capacity, made
of stainless steel or other corrosion-resistant material and fitted with
air-tight covers.
IS: 172711967
14.3 Reagents
a) Unless otherwise indicated, all reagents used shall be analytical
reagents. Water used shall be distilled water, unless otherwise
stated.
b) Standard sodium hydroxide - Prepare a 1900 f PO10 N sodium
hydroxide. solution and standardize to f OS001 JV. Use water
that has been boiled until free of carbon dioxide for preparing the
solution.
c) Hydrochloric acid - sp gr l-16.
d) Standard hydrochloric acid - Prepare approximately 0.05 X hy-
drochloric acid and standardize to f O*OOO1 JV. Standardize
the hydrochloric acid, for each day’s tests, against an approximately
@05 N standardized sodium hydroxide solution.
e) Phenoi~hthalein indicatory solution - Dissolve one gram of phenol-
phthalein in 100 ml of ethanol ( 1 : 1 ).
14.4 Initial Preparation

14.4.1Weigh out three representative portions of the pozzolana, each
of 12.50 f 0.05 g. Place one portion in each of the three reaction con-
tainers and add 25 ml of the O+Ol X sodium hydroxide solution. To a
fourth reaction container, add 25 ml of the standard sodium hydroxide solu-
tion to serve as a blank. Seal the four containers and gently swirl them to
liberate trapped air.
14.4.2 Immediately after the containers have been sealed, place them in
a liquid bath maintained at 80.0 f 1.0%. After 24 f 4 h, remove the
containers from the bath and cool them under running water for 15 -b 2
minutes to below 3O’C.
14.4.3 Immediately after the containers have been cooled, open them
and filter the solution from the total residue. Use a porcelain Gooch cruci-
ble fitted with a disk of rapid low-ash filter paper, setting the crucible in a
rubber holder in a funnel. Place a dry test tube of 35 to 50 ml capacity in
the filter flask to collect the filtrate and seal the funnel in the neck of the
filter flask. With the aspirator in operation or the vacuum line open, decant
a small quantity of the solution into the filter paper so that it will seat properly
in the crucible. Without stirring the contents of the container, decant the
remaining free’liquid into the crucible. When the decantation of the liquid
has been completed, discontinue the vacuum and transfer the solids remain-
ing in the container to the crucible and pack in place with the aid of a
stainless steel spatula. Then apply and adjust the vacuum to approximately
380 mm of mercury. Continue the filtration until further filtration yields
filtrate at the approximate rate of one drop every 10 seconds. Reserve the
filtrate for further tests. Record the total time for which the vacuum is
45
Isr1727-1967
applied as the filtration time. Every effort shall be made to achieve an equal
filtration time for all samples in a set, by uniformity of procedure in the
assembly of the filtration apparatus and the packing of the solids in* the
crucible.
14.4.4 Filter the blank according to the procedure described in 14.43
Apply the vacuum for the same length of time as the average filtration time
for the three specimens.
14.4.5 Immediately following the completion of filtration, stir the filtrate
to assure homogeneity. Then take an aliquot of 10 ml of the filtrate and
dilute with water to 200 ml in a volumetric flask. Reserve this diluted solu-
tion for the determination of dissolved silica and reduction in alkalinity.
NOTE-In some cases, it may become necessary to add more than 25 ml of sodium
hydroxide solution either due to the solution becoming viscous or to the formation of a
gel. In such cases, the quantity of sodium hydroxide may be increased.
14.5 Silica Release Test
14.5.1 Transfer 100 ml of the dilute solution to an evaporating dish,

preferably of platinum. For the sake of celerity in evaporation, add 5
to 10 ml of hydrochloric acid and evaporate to dryness on a steam-bath.
Without heating the residue any further, treat it with 5 to 10 ml of hydro-
chloric acid, and then an equal amount of water, or at once pour 10 to 20 ml
of hydrochloric acid ( 50 percent ) upon the residue. Cover the dish and
digest for 10 minutes on the bath or a hot-plate. Dilute the solution
with an equal volume of hot water ( see Note ) and reserve the residue.
NolZ -The washing of silica precipitates can be made more effectively by using hot
hydrochloric acid ( one percent ) and then completing the washing with hot water.
14.5.2 Again evaporate the filtrate to dryness, baking the residue in an

oven for one hour a 105°C to 110°C. Take up the residue with 10 to
15 ml of hydrochloric acid ( 50 percent ) and heat on the bath or hot-plate.
14.55 Dilute the solution with an equal volume of hot water and obtain
and wash the small amount of silica it contains on another filter paper.
14.5.4 Transfer the papers containing the residue on to a platinum cruci-
ble ( see Note ). Dry and ignite the papers, first at a low heat until the car-
bon of the filter paper is completely consumed without inSaming, and finally
at 1 100°C to 1200°C until a constant weight is reached.
Norm-Thecmptycruciblemaybc weighed if one wishen to know for his own
information, the magnitude of impurities in the residue of silica
14.5.5 Treat the silica thus obtained, which wilI contain small amounts
of impurities, in the crucible with a few drops of water, about 10 ml of
hydrofluoric acid, and one drop of sulphuric acid, and Mporatc cautiously
to dryness. Finally heat the residue at 1050°C to 1100°C f& 1 to 2 minufu
46
xsrl727-1961
cool and weigh. The difference between this weight and the weight previ-
ously obtained represents the amount of silica.
145.6 Make a blank determina tion, following the same procedure as
dexribed in 14.5.1 to 14.5.4 using the same amount of dilute solution from
the blank and the same amounts of reagents.
14.5.7 Calculate the silica concentration in the solution originahy filtered
( su 14.4s ) as follows:
sc=(Wr-- W, j x 3 330 ( see Note )
where
SC = ;zoFtration of silica in milliioles/litre in the original
w, = grams bf silica found in 100 ml of the dilute solution, and

w, = grams of silica found in the blank.
NOTE-The dilute solution analyscd is equivalent to 5 ml of the original or
( Wl - W,) x 1000
millimolcs ofsilica conscqucntly one litre of the original filtrate
60.06
Would cpntain ‘y X b+g x ( WI - WE ) or 3 330 ( WI - IV, )millimola of r&x.
14.6 Reductionin AUulinity

14.6.1 Transfer a 20 ml aliquot of the dilute solution obtained as in 14.4
to a 125 ml Erlenmeyer flask. Add 2 or 3 drops of phenolphthalein solution,
uad titrate with 0.05 N hydrochloric acid to the phenolphthalein end point.
14.63 Calculate the reduction in alkalinity as follows:
Re= 2y(y,- V,) x IO00

where
R, = the re&ction in alkahnity, millimoles/litre;
N- normality of the hydrochloric acid used for titration;
v. = volume of dilute solution used in ml;
v, = volume of hydrochloric acid used in ml to attain the
phenolphthalein end point in the blank; and
VS w volume of hydrochloric acid used in ml to attain the
phenolphthalein end point in the test sample.
w.1 Appmtum
l5.1.1 The standard ‘Le chatelier’ flask confoaming to the dimenrionr
showBitlFii..shallbeused.
47
EWLA
TWO 0.1ml GRADUA 7 ml CAPACITY

EXTENDING ABOVE
BELOW 0 MAR
AudimeAmsinmillimetrts.
FIG. 9 ‘ LE CHATBLIER’FLASK FOR SPECIFIC GRAVITY T~sr
48
--
15.11 Warn Bath -A suitable water bath to accommodate the ‘h
l+~ttlitr’fli%SkShall&wed.
1542 MateAl - Kerosine f%eeof water or naptha having a spcdk gravity
notlessthan@7313shallbeused.
15.5 Procedure
153.1 Specific gravity of pozzolana shall be determined on the material
as received, unless otherwise speciiied.
153.2 Fill the Baskwith kerosine or naptha to a point on the stem between
the zero and the 1 ml mark and replace the stopper. Then immerse the
flask in a constant temperature water bath, maintained at about room
temperature, for sufficient interval to avoid variations greater than f 02%
in the temperature of the liquid in the flask. Take the reading of the liquid
intheflask.
15.53 Introduce a weighed quantity of pozzolana into the flask, taking
care that no portion of it adhere to the inside of the flask above the liquid,
by slightly vibrating the flask. Replace the stopper and roll the flask in an
inclined position to expel any air bubble in the pozzolana. The level of the
liquid will be in its final position at some point of the upper series of gradua-
tions. The reading shall be taken after the flasksimmersed in the water bath.
NOTE l-A~b~pPdonthe~blemrrykuwdwhcn~~m~tbcBuL.
Nur~ 2--e&rlrnuybeheldin8vatiulpaitioninthcmtahthby~ob
a burette clamp.
15.4 Meuladon-The difference between the first and final e

reprtse@s the volume of liquid displaced by <theweight of cement used in
the test. SpecXc gravity shall be calculated as follows:
Weight of pozzolana in g
SpecXc gravity q
Displaced volume in ml
15.5 B-Duplicate determination of ape&fic gravity by
this method shall agree within @Ol.
49
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Telephones: 323 0131,323 8375,323 9402
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Cenfral Uborato& : -%. L..z&.+_fl., Telephone
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“ha*,.
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inspection OftIces (With Sale Point) :
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Printed at Simco Printing Press, Delhi, India

AMENDMENT
NO. 1 OCTOBER 1991
TO
IS 1727: 1967 METHODS OF TEST FOR POZZOLANIC
MATERIALS
( ~~~ Revision j
( Page 6, chse 3.1 ) -Substitute the following for the existing clause :
‘3.1 Hydrated Lime - Standard hydrated lime supplied by National Gnmcii for
Cement and Building Materials, New Delhi shall be used in the tests. The
standard hydrated lime shall have the following composition :
CaO - 96 f 0.5 percent
MgO - 1 f 0.5 percent
SiO2, Max - 1.0 percent
Insoluble residue, Mar - 1.0 percent
(Page 6, clause 3.2 ) - Substitute the following for the existing clause:
‘32 Cement - Cement for use in the tests shall be 33 grade ordinary Portland
cement conforming to IS 269 : 1989.’
(Puge 6, clause 5.1.1) - Substitute ‘IS 1070 : 1977’for ‘IS 1070 : 1960’.
(Page 6, foot-notes ) - Delete foot-notes No. 2 and 3, and substitute

‘Spccificafion for 33 grade ordinary portland cement (/o(lA rev&ion) ’ for ‘Specifiatioo lot
o&nary. rapid-hardenrng and low heat Portland cement (rev&J)‘; and ‘Spccifiation for
water for general lahoralory use (second ~evi.&m~ / or ‘Specification for water, distilled quality
(rcvi.wd).’
(Page 28, cluuse 9.7, Note) -Substitute the following for the existing note:
‘NOTE - For curing the s cimen at the specified relative humidity and tern nturc as giverr
above, it is recommended I%at the controlled humidity and temperature cham c r developed by
National Council for Cement and Building Malcrials may be used for proper pctformaaa.’
(CED2)
Printed at Simco Printing Press, Delhi, India

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IS : 1727 - 1967

UDC 666.95.014/.017 : 691.545

DR IQBALAU Hyderabad Engineering Research Laboratory,

&$0; Irrigation & Power Research Institute, Amritur

BUREAU OF INDIAN STANDARDS

Panel for Revision of IS : 1727-1960, BDC 16/Pl

SHRI C. A. TAN~JA( Alternate )

Sriar P. J. JAGUS Concrete Association of India, Bombay

constant ( by batching by absolute volume ) such an anomaly would not

assessment of the propert& and potentialities of the different poz~olani~

,S.1.2The following reagents and special solutions are required:

Loss on ignition, percent = +- x 100

5.4.5.1 To this amount of silica, add the amount of silica recovered

5.5 Combined Ferric Oxide and Alumina

5.5.1 To the solution obtained in 5.4.6 ( approximately 300 ml ) add 2

6.0 The fineness of pozzolana shall be determined by the procedure given

6.1 Determination of Sped& Sdace of Pozzolana

FLAT 3mm WIDE

PERFORATED METAL DISC

MANOMETER ENLARGED DETAIL OF CELL AND PLUNGER

FIG. 1 BWNE AIR PERMEABILITYAPPARATUS

6.1.3.2 Bulk volumeof compactedbed of powder - The bulk volume of the

TABLE 1 DENSFlY OF MERCURY, VlSCOSlTY OF AlR (IS) AND 4;

16 13.56 0.000 178 8 0*013 37

6.1.3.3 Prejaration of sample -The contents of a vial of the standard

cell diameter. A quantity of cement determined in accordance with 6.1.3.4

6.1.5 Cakulations - Calculation of specific surface values shall be made

8s ............ ... .............. ...... (a)

TABLE 2 VALUES FOR POROSITY OF CEMENT BED

6.2 Determhudon of Fineness by Sieving

6.2.3 P@amtion of Saqlu - A representative sample shall be taken iu

percentage of mai;erial passing each sieve on wet sieving shal1 be reported to

8. DETERMINATION OF INITIAL AND FINAL SETTING TIME

9.2 Size and Number of Test Specimens

9.2.1 The tests specimen shall be 50-mm cubes.

9.2.2 Unless otherwise specified in the relevant specification for the

All dimsions in milljmetre.

shown in Fig. 3. It shall comply with the limiting dimensions shown in

All dimenaiona in millimctres.

FIG. 3 MIXING BOWL

9.3.2.4 Scrapn - The scraper shall consist of a semi-rigid rubber blade

93.4 Tamping Rod - The tamping rod shall be made of a non-absorptive,

9.5 Preparation of Mortar

9.5.3 Determination of Flow

9.6 MonIding Test Specimens - Immediately following the preparation

10. DETZRMINATION OF COMPRZSSIVE STRZNGTH OF

102 size of spedmens -The test specimens shall be 50 mm cubes.

105 Preparation of Mortar

for 24 hours after completion of compaction. At the end of that period,

11. DETERMINATION OF TRANSVER!3E STRENGTH OF THE

permitting the preparation of three specimens at a time. The internal

11.3 Size and Number of Test Specimens

11.5 Prepmration of Mortar

All dimcnsiau in miuilnetra.

The temperature of curing water shall be maintained at 27 f 2%. The

12. DETERMINATION OF DRYING SHRINKAGE IN

TABUS -IS VARIATIONS ON WE3GElTS

12.3 Size and Number of Test Specimens

12.7 Roetdura of Test