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Sorptivity of Mortar
Sorptivity of Mortar
Sorptivity of Mortar
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Hull
However, it is a fact that in construction engineer- As noted elsewhere,14this theory marks significant
a
ing our materials are rarely saturated in use and the advance in the analysis of water movement in building
permeability is the wrong parameter for modelling of materials in several respects. First, the theory(as
capillary flowsin building structures. The reason is equations (1)-(3) show) firmly unites the concepts of
clear. At complete saturation, the suction exerted by a suction and permeability. Second, the dependence of
material is reduced to zero; andthe(saturated) both permeability and suction on water content 8 is
permeability tells us nothing about the driving force made explicit. Third, the very extensive work done in
for capillary flows. Recognition of this has motivated soil physics provides a well-developed mathematical
work over many years on the capillary suction proper- structure based on the general theory of non-linear
ties of building materials.** Unfortunately, the suction diffusion processes for the analysis of water flow in
property is much more difficult to measure than the building elements.
permeability; and like the permeability it also tells an
incomplete story. Sorptivity
What is required is a physical theory of capillary
flow in unsaturated materialswhich embodies the idea Thesorptivity S is obtained by consideringthe
of Darcianflow in a porous materialin response to the application of equation (4) tothe one-dimensional
capillary force arising from its own pore structure, at case of water absorption into an initially dry porous
all fractional saturations. Unsaturatedflow theory (as solid (see Fig. l ) . Theboundaryconditionatthe
developed for water transportin soils23) doesprecisely wettedsurface is 8 = 8,. The initial condition is
this. The physicsof the flowis expressed in the 8 = Bo, where, for a dry material, 8, is close to or
extended Darcy equation equal to zero. The cumulative water absorption (per
unitarea of theinflow surface) i increases as the
4 = K(8) (1) square root of the elapsed time t
in which q is the vector flow velocity, K the hydraulic
conductivity and F, the capillary force. Both K and F,
depend on the water content8. The hydraulic conduc- S is related mathematically to D (or K , Y) because
tivity atsaturation is theconventionalsaturated solving equation (3) or (4), for example by the method
permeability. In addition the capillary force is ident- of Philip,*'gives 8(x, t ) , the watercontent distri-
ified with the gradient of the capillary potential (or butions at all times and positions. It is found, for this
suction) Y one-dimensional case only, that 8 is a function of the
single variable d, = xtr'"*, so thatthe cumulative
absorption at any time t is given by
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Water sorptivity of mortars and concretes
Water
reservoir
235 mm
x=o
I.Oy x 38min
o 57min
x + m 97min
m + + 208min
0.8 X
o
.
m
+ + o
271 rnin
o m
m + o
6
o‘6 t x 0
x
0
0
m
m
+
+
+
+
o
+
0
0
-1
0.0
I
0.2
I
0.4
0,
I
0.6
I
0.8
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Hall
1sr
tl/':minl/2
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Water sorptivity of mortars and concretes
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Hall
m
between 6 and 8, varyinglittle between materials.
m 0 O While further experimental confirmation is necessary,
0
it appears probable that for engineering calculations,
A
we may regard equation (IO) as universal. If so, the
A A
A 'A
functional dependence of sorptivity on initial water
A content is also universal (and asgiven in reference IO).
For practical purposes (assumingB = 7), this may be
0.0 U I I I written as
2000 2100 2200 2300 2400
Density: kg/m3 S,/So = (1 - 1.088i,)1'2 (1 1 )
(a)
where S, is the sorptivity measured on a dry sample
Mixes
2.0 Cernentilimeisand (8, = 0) and S, the sorptivity measured on the same
m Masonry cementisand samplewith an initial,uniformnormalizedwater
A Vinsol resin Dlasticized OPCisand
content 8, = &.
\ 0
Dependence of sorptivity on temperature
The sorptivity rises slowly with increasing tempera-
ture. It has been shown4 that the sorptivity at any
temperature is proportional to quantity(o/q)"*,where
a is the surface tension andq is the viscosity of water.
This is exactly as predictedtheoretically: (o/q)'!'
A
A A
increasesfrom about7m"2/s1'2at 5°C toabout
I I I l J
0.0
1600 1700 1800 1900 2000 2100
10m"2/sl'2at 35°C.
Density kgirn'
(b)
Sorptivity measured with dzfferent fluids
Fig. 6 . Sorptivity variation in morrurs and concretes: ( a ) A sorptivity measurement can be made with any wet-
concrete sample^;'^ (6) mortar sampIes,13 increasingly rich ting fluid. The sorptivity as conventionally measured
in cement,frorn left t o right
is the water sorptivity (or hydraulic sorptivity),using
pure water as the absorbed fluid. For other wetting
usually dry(although they are rarelycompletely fluids, themeasuredsorptivityagain varies4 asthe
saturated). It follows that a key question is: 'Given quantity (aiq)". The small variation in water absorp-
thatthesorptivityofamaterialmeasuredunder tion ratewith different salt solutions notedby MacInnis
laboratoryconditions is known,what willbe its andNathawad2'probablyarosefrom the
small
sorptivity in situ at other initial water contents?' changes in viscosity and surfacetensionrelative to
For a material of knownD ( 8 ) ,the cumulative water pure water.I4
absorptioncan be foundasafunction oftime by
Philip's method25 for any uniform initial water content Relation between sorptivity and other
8,. Consequentlythesorptivitycanbefoundasa
function of 8,. Hall et al. reported" a study of the
measures of water absorption
dependence of the sorptivity of brick on the initial There has been muchdiscussion35 recently about
water content. This showed excellent agreement with thestrengthsandshortcomingsofanumberof
the predictions of unsaturated flow theory. A number proposed test methods for estimating water absorp-
of approximate expressions are known which relate tionandtransmissionproperties.Much of thedif-
the sorptivity to the diff~sivity~',~* and which would ficulty stemsfromthefactthat these methodsare
allow corrections for different initial water contents to treatedempirically andarenotsupported by any
be made. It should be emphasized that initial the water underlying physical theory of capillary flow. In fact,
content must be uniform; if it is not, the initial con- given suchatheory (even if incomplete)a variety
dition for equation (6) is not met and t"' absorption of methodsshouldprovide estimatesofthesame
behaviour will not be observed.Thecorrectionfor materialproperty.It is interesting,
therefore, to
initial watercontent canonly bemade if the functional analyse the proposed test methodsin terms of unsatu-
dependence of the diffusivity on water content 8 is rated flow theory. From such analyses, data from any
known. While our knowledgeof D forbuilding method can in principle be used to obtain anestimate
materials remains quite limited, there is e ~ i d e n c e ~ , ' ~ofthesorptivity.InfactonlytheISAThas been
56 Magazine of Concrete Research, 1989, 41, No. 147
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Water sorptivity of mortars and concretes
1Omin ISAwaterabsorptionrate(ISA,,) by the Fig. 9. Comparison of ISAT and sorptivity test data f o r
formula concrete (1 :2 :4 OPClsandlgravel aggregate; water :cement
ratio 0.7; sorptivity 0.115 mm/min"2); the extremely small
total absorption compared with Fig. 8 should be noted
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Hall
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Water sorptivity of mortars and concretes
Conclusions
Thetheory of unsaturated flow asdeveloped in
soil-water physics offers agooddescription of the
processesofcapillary flowin porouscementitious
materials.Thefundamentalmaterialpropertiesare
the hydraulic diffusivity D,the moisture potential Y
andthehydraulicconductivity K . Of thesethree
quantities, only two are independent. The hydraulic
sorptivity S is a derived quantity of the theory which
(W
may easily be determined in a simplecapillary absorp-
Fig. 12. Surface absorption test arrangements in which tion test in the laboratory. The sorptivityis mathemat-
lateral spreading from the source is minimised: ( a ) measure-
ically related to the hydraulic diffusivity. All simple
ment on an attached core; ( b ) source with guard ring in
which the absorption from the central compartment only is water absorption test procedures in principle provide
measured data fromwhich the sorptivity canbe estimated. How-
ever, the geometrical arrangements in the currentfield
methods are not ideal for this purpose. Furthermore,
teristic of capillary d r ~ i n g ' ~ that
. ~ ' steep gradients of the difficulty of bringing the sample to a satisfactory
water content develop near the surface of the material initial state of dryness presents a major difficulty for
(say the top 10-20mm). all field methods.
The ISAT could beimproved in some respects.8 For concretes and mortars, sorptivity data obtained
Prescribing a circular source of standard radiuswould in the laboratory showreasonablysystematic vari-
eliminate some variability, bearing in mind that the ation with mix andcuringhistory. A casecan be
characteristic time for absorption from the circular made for including a measurement of the sorptivity
source is ri f ' / S 2 .Again, the slope of the cumulative parameter routinely in researchwork onconcrete
absorption i against t'" is a bettermeasureofthe materials.
sorptivity than the single point measurement.
There are also two simple ways of eliminating (or
greatly reducing) the lateral spreading from theTSAT Acknowledgements
source. One (Fig. 12(a)) is to drill into the test surface The Author gratefully acknowledges the support of
with a core bit of the same diameter as the source to the UK Science and Engineering Research Council,
isolate a cylindrical prism of material (but without and the contributions of W. D. Hoff, R. J. Gummer-
detaching it). The secondis to use a guard ring on the son, A. N. Kalimeris, M. Skeldon, T. K. M. Tse and
source (Fig. 12(b)), measuring water absorption only M. R. Yau to the work described.
from the central circular compartment.
Methods involving water absorption from cylindri-
cal drill holeshave several practicalattractions. Appendix
Procedure for measuring the hydraulic sorptivity4."
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Hall
measured at intervals by weighing thespecimen. A water absorption rate per unit source area eventually
top-pan balance weighing to 0.1 g is suitable, but a reaches a steady finite value U, = 2S2/(nfr0).How-
balance weighing to 1 g is adequateunder some ever, no results appear tobe available for intermediate
circumstances (for example for whole bricks or other times, althoughthethree-dimensionalunsaturated
large specimens). Surfacewater on the specimen flowcould be modelled numerically, using the full
should be mopped off with a dampened tissue. Each three-dimensionalunsaturated flow equation which
weighing operation should be completed as quickly as can be developed from equation (3).
possible (within 30 S ) . The clock should notbe stopped
during weighing. A minimum of five points is necess- Absorption from a cylindrical source
ary to define a good sorptivity plot and a somewhat Two-dimensional radial capillary absorption from
largernumber is desirable. The dimensions of the a cylindrical source, radius r,, has been analysed by
specimen and the temperature should be noted. Philip." Usingthe sharp wet-frontapproximation
Analysis of results. S is defined as the slope of the i gives expressions for the absorptionrate U" and
against t'" line, where i = Aw/AQ*(in which Aw is the cumulative absorption i (per unit area of cylindrical
increase in weight, A the cross-sectional area and e* supply surface) at all times t . Defining dimensionless
the density of water). If the i against t"' data are well variables
represented by a straight line, S should be determined
by a least-squares fit of i on t112.The origin should not
be included as a datum point because an intercept at
t = 0 is frequently found on extrapolation of the best and
line to the remaining points. If the i against t"* plot is
not linear but shows some systematic curvature, no
sorptivity can be derived in this simple way (but see
Hall and Tse13 for the use of the equation i = A +
St1'2 - C t ) . gives
The sorptivity is proportional to (o/r])"',where o is
the surface tension and r] the viscosity of the absorbed T = [($ - l ) exp (4/7cU) + l] (14)
fluid. The sorptivity rises with temperature. Data on
the sorptivityobtainedin thelaboratorywithout and
deliberate temperature control can be normalized to a
standard reference temperature of 2OoC by applying a
multiplying factor to the measured sorptivity value.
Fullest details of the test material should be noted, For small T, U = (zT)-',", sothat U, = ST-1'2/2,
including the direction of flow in the sorptivity test in and, at large T, U = 2(ln T)-I
relation, for example, to the brick face or the bedding
plane of a building stone. Useful supplementary data
includethedry bulk density and the vacuumsatu- References
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Millimetres/(minutes)'/' are convenientunitsfor algebraic infiltration equations. Soil Sci., 1957, 84, 257-264.
2. HALL c. Water movement in porous building materials-l.
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10-~m/sl.~. 12, 117-125.
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Water sorptivity of mortars and concretes
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