Zhu2015.nonlinearity of One-Dimensional Creep of Soft Clays
Zhu2015.nonlinearity of One-Dimensional Creep of Soft Clays
DOI 10.1007/s11440-015-0411-y
RESEARCH PAPER
Abstract This study focuses on the quantitative used in the formulation are correlated with Atterberg lim-
description of the evolution of creep coefficient (Cae) with its, allowing us to suggest a relationship between Cae,
both soil density and soil structure under 1D compression. Atterberg limits and inter-particle bonding for a given soil.
Firstly, conventional consolidation test results on various Finally, the validity of the proposed formulation is exam-
reconstituted clays are selected in order to investigate the ined by comparing experimental and predicted Cae values
evolution of Cae with void ratio of soils, which can be for both reconstituted and intact samples of natural soft
described by a simple nonlinear creep formulation. Sec- clays. The proposed formulation is also validated by
ondly, the contributions of the inter-particle bonding and comparing the computed and measured void ratio with time
debonding for soft structured clays to Cae are analyzed on two intact clays.
based on test results on intact and reconstituted samples of
the same clay. A material constant q, function of the Keywords Atterberg limits Creep Density
bonding ratio v, is introduced in order to quantify the Destructuration Oedometer test Soft clays
contribution of the soil structure to Cae, and a nonlinear
creep formulation accounting for both soil density and soil
structure is finally proposed. Furthermore, the parameters 1 Introduction
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in a more precise way a linear decrease in Cae with the void correlations could be established in order to estimate the
ratio in a double logarithm plane based on results on var- value of Cae from Atterberg limits for a given natural soft
ious reconstituted clays. For intact natural soft clays, the clay. Then, the proposed function is validated by compar-
value of Cae depends highly on the destructuration, as ing the estimated and experimental Cae values.
demonstrated by Karstunen and Yin [10], Leroueil et al.
[15], Mesri and Godlewski [17] and Yin et al. [33], etc.
Therefore, Cae is generally not constant but dependent on 2 Nonlinear creep related to soil density
both the void ratio and the soil structure (or inter-particle
bonding and debonding) of soft soils. However, few studies 2.1 Experimental evidence
have been devoted to a quantitative description of the
nonlinear evolution of Cae due to changes of both soil Conventional consolidation tests on various soft clays with
density and soil structure in natural soft clays. Furthermore, different mineral contents and Atterberg limits were
for correlating Cae to clay physical properties (e.g., Atter- selected for this study. In this section, all the selected data
berg limits), an average value or the value of Cae corre- are based on reconstituted samples to eliminate the influ-
sponding to a final high stress level in conventional ence of soil structure. Some physical properties of the
oedometer tests has usually been adopted. Since Cae is not selected clays are summarized in Table 1. According to the
a constant, it is necessary to seek a reference value of Cae chart shown in Fig. 1, the selected soils consist of low
to re-establish the correlation. plastic clays, high plastic inorganic clays and high plastic
In this study, therefore, we focus on the quantitative silty clays. Since the void ratio (e) is a physical state of
description of the evolution of Cae with both void ratio and soils representing the soil density and the deformation
soil structure under the condition of applied stresses potential, the Cae values for all the selected clays are
exceeding the yield stress. For this purpose, available test individually plotted against the void ratio in a double
results on intact and reconstituted samples of natural soft logarithmic plane, presented in Fig. 2. All the results show
clays are selected for analyses. We also carry out con- that log(Cae) is linearly related to log(e).
ventional consolidation tests on reconstituted and intact
samples of several clays for expanding our data base. The 2.2 Nonlinear creep formulation accounting
values of Cae corresponding to liquid and plastic limits for void ratio
(CaeL, CaeP) are then estimated as reference values, based
on which Cae could be expressed as a function of one of the The consideration of the density and void ratio has been
reference values Caef (=CaeL or CaeP), the water content addressed by Yin [27] based on Hong Kong marine clay.
(w) and the inter-particle bonding (v). Furthermore, Based on the results in Fig. 2, the nonlinear creep
Table 1 Summary of creep coefficient of reconstituted clays under normally consolidated state
Clay Depth/m Cae Applied stress corresponding m e0 Gs wL IP
to Cae/kPa
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150 Nanjing clay(1) schematic plot of the compression curves of intact and
CL: Low plastic inorganic clays, sandy and silty clays Wenzhou clay(1)
OL: Low plastic inorganic or organic silty clays
Lianyungang clay(1)
reconstituted clay samples. For a given inelastic strain level
CH: High plastic inorganic clays
OH: High plastic fine sandy and silty clays Haarajoki clay Dep, the bond degradation results in the current stress r0v
Suurpelto clay
100 *: Present study
Vanttila clay
reaching point A instead of point B (assuming no
CH Murro clay destructuring). Corresponding to stress r0v at DeP, we define
an intrinsic stress r0vi , which is the stress for a reconstituted
IP
HKMC
U-line: IP=0.9(wL-8)
Zhoushan clay*
50 Kaolin* sample at the same inelastic strain increment (point C).
OH Nanjing clay(2)
Based on this plot, a bonding ratio can be defined by v ¼
Wenzhou clay(2)
A-line: IP=0.73(wL-20)
CL
OL
Lianyungang clay(2)
r0v r0vi 1 with an initial bonding ratio of v0 ¼
Shanghai(1)
0 Shanghai(2)*
.
0 50
wL
100 150
Zhangzhou clay r0p0 r0pi0 1 (similar to Gens and Nova [8]; Yin et al. [33,
34]). When the strain increases, the inter-particle bonds are
Fig. 1 Classification of soils by liquid limit and plasticity index progressively broken and v decreases from its initial value
v0 toward zero, corresponding to a state where all the bonds
formulation based on Finnish clays proposed by Yin et al.
are completely destroyed, as shown in Fig. 3.
[34] can be adopted:
Adopting this concept, we consider that the difference
Cae =Caef ¼ ðe=ef Þm ð1Þ between the values of Cae at point A and point C is due to
the effect of soil structure. Defining the creep coefficients
where Caef and ef are reference values of Cae and e,
Cae(I) and Cae(R) at points A and C (Fig. 3), the additional
respectively (the initial in situ void ratio e0 was used as ef
creep induced by destructuration (or inter-particle
by Yin et al. [34]) and m is a material constant representing
debonding) can be written as:
the slope of the log(Cae)–log(e) curve which can be mea-
sured in a straightforward way (summarized in Table 1 for DCae ¼ Cae ðI Þ Cae ðRÞ ð3Þ
all clays). It is worth noting that Cae is conventionally
3.2 Nonlinear creep formulation accounting for soil
defined as the slope of the secondary compression line with
structure
the logarithm of time, which is reasonable for design
purpose in civil engineering, but resulting in a negative
To investigate the contribution of soil structure on Cae,
void ratio during creep under long periods of time, whereas
conventional consolidation tests on both intact and recon-
Eq. (1) imposes a value of e converging toward zero but
stituted clay samples of the same clay are necessary.
remaining always positive.
Table 2 summarizes the available results of 1D creep tests
The reference point (Caef, ef) can be arbitrary selected.
on both intact and reconstituted samples of ten different
However, it could be of interest to select specific values of
clays (corresponding to the first ten clays in Table 2,
the reference void ratio. The void ratio at the liquid or
including the tests on Shanghai clay performed in this
plastic limit (eL or eP) is usually adopted to establish the
study). The classification of these clays is shown in Fig. 1.
equations for compressibility [20, 21]. These two values
Figure 4 presents the plots of Cae(I) with the bonding
can be easily determined from the liquid or plastic limits
ratio v, where Cae(I) in these graphs was directly measured
wL and wP which are usually available physical properties
from tests on intact clays. Note that Cae(R) was estimated
of clayey soils. Along these lines, two representative points
by Eq. (1) from experimental data on reconstituted clays at
(corresponding to eL and eP) on the log(Cae)–log(e) curve
the corresponding void ratio (point C in Fig. 3) and served
can be alternatively used as reference points. Based on
as the reference for the effect of destructuration. It can be
Fig. 2, both CaeL and CaeP corresponding to the void ratios
seen that Cae(I) decreases linearly with the decreasing of v
eL and eP can be obtained and Eq. (1) can be rewritten as
in a logarithmic scale. Based on the concept used to define
Cae ¼ CaeL ðe=wL Gs Þm or Cae ¼ CaeP ðe=wP Gs Þm ð2Þ v (Fig. 3), we can express the contribution of the soil
structure to the creep coefficient by the index q:
3 Nonlinear creep related to soil structure q ¼ Cae ðI Þ=Cae ðRÞ 1 or q ¼ DCae =Cae ðRÞ ð4Þ
where q is always positive. In order to investigate the
3.1 Experimental evidence relation between q and v, values of q for all the selected
clays were estimated by Eq. (4) and plotted versus v in
During conventional consolidation tests on intact samples Fig. 5. It can be observed that q presents a linear
of natural soft clays, the shape of the post-yield compres- relationship with log(v), which can be expressed as:
sion curve is significantly influenced by the debonding
process during straining [10, 13, 23]. Figure 3 shows the q ¼ n logðv=v0 Þ þ q0 ð5Þ
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Fig. 2 Creep coefficient versus void ratio in double logarithmic scale for different reconstituted clays
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Intact clay
Intact clay Intact clay
Reconstituted clay
0.06 Reconstituted clay 0.03 Reconstituted clay
0.04
0.04 0.02
0.02
0.02 0.01
0 0 0
1 10 0.01 0.1 1 10 0.1 1 10
0 0 0
0.1 1 10 0.1 1 10 0.1 1 10
Lianyungang
0.04 clay (1) 0.02
0.02
0.02 0.01
Lianyungang
clay (2)
0 0 0
0.1 1 10 0.1 1 10 0.1 1 10
Fig. 4 Creep coefficient of intact and reconstituted clays versus bonding ratio
were selected. Figure 6a, b presents the plots of CaeL with CaeP ¼ 0:0013wL 0:0013Ip 0:0209 ð8Þ
Atterberg limits, from which the following relation could
be obtained with a correlation coefficient R2 = 0.9336: From these correlations, it appears that the choice of
CaeL as the reference value for Cae in Eqs. (2) and (6) is
CaeL ¼ 0:0007wL 0:0223 ð7Þ preferable given the higher correlation coefficient. Thus,
Similarly, Fig. 6c, d shows the correlations for CaeP the CaeL with wL can be used as reference in Eq. (6), and
indicating that the optimized correlation is obtained by the Eq. (6) is rewritten as,
using both the liquid limit and the plasticity index with a Cae ¼ ðn logðv=v0 Þ þ q0 þ 1ÞCaeL ðw=wL Þm ð9Þ
correlation coefficient R2 = 0.6913:
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Based on all the estimated values of m shown in Eq. (6) 4.3 Correlation of n with Atterberg Limits
for 15 reconstituted clays, the correlations between m and
Atterberg limits were fitted. Figure 7 shows that the Figure 8 presents the correlations between the material
optimized correlation is obtained by using both liquid constant n shown in Eq. (6) and Atterberg limits based on
limit and plasticity index with a correlation coefficient test results on both intact and reconstituted samples of ten
R2 = 0.5217: clays. It can be observed that the magnitude of n decreases
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(a) (b)
0.06 C eL = -0.0274 +0.0011wL -0.00048IP
R2 = 0.9247
0.04
y = 0.0007x - 0.0223 0.05
0.05
eL
R² = 0.9336 0.04
0.04
0.03
eL
0.03
eL
0.02 0.02
0.02
0.01
0.01
0
0 80
60 70
0
0 50 100 50 60
40 50
Liquid limit, wL 30 4 Liquid limit, wL
Plasticity index, IP 20 0
(c) (d)
0.03 C eP = -0.0209 + 0.0013wL 0.0013IP
R2 = 0.6913
y = 0.0012x - 0.0218
0.02 R² = 0.6453 0.03
0.03
eP
eP
0.02
0.02
eP
0.01 0.01
0.01
0
0 80
60 70
0 50 60
40
0 10 20 30 40
50 Liquid limit, wL
0
Plastic limit, wP Plasticity index, IP 3 4
20 0
2
2
m
m
1 1
1
1
0.5 0.5 0
0 80
70
60
50 60
0 0
0 50 100 0 20 40 60 80
40 50
Liquid limit, wL Plasticity index, IP 30 40 Liquid limit, wL
Plasticity index, IP 20
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1.5
y = -0.0149x + 1.5914 1.5
1 R² = 0.5937
1 1
n
n
n
cae
0.5
n
0.5
0.5 0.5
0
0
80
70
0 50
0 60
0 50 100 0 10 20 30 40 40 50
30 Liquid limit, wL
Liquid limit, wL Plasticity index, IP 40
Plasticity index, IP 20
1
0.6 0.6 1
0.8
y = 2.34e-0.047x y = 0.8403e-0.056x 0.8
0.6
R² = 0.7641 R² = 0.714 0.6
0.4 0.4 0.4
0.4
0.2
0.2
0.2 0.2 0
0 80
70
50 60
0
0 50 100
0
10 30 50 70 40 50
30 40 Liquid limit, wL
Liquid limit, wL Plasticity index, IP Plasticity index, IP 20
80
n ¼ 2:4630 0:0585wL þ 0:0532IP : ð11Þ
This study
60 y = 0.8381x - 16.438 4.4 Correlation of q0 with Atterberg Limits
R² = 0.9587
IP = 0.73(wL-13)
As mentioned above, q0 is the initial value of q corre-
IP
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5 Discussions selected in this study together with the two lines repre-
senting the above correlations. The differences between
5.1 Correlation between IP with wL these two lines and the experimental points are rather
small, and we could consider one or the other correlation
A certain relationship between IP and wL is apparent. In the for our own materials. In order to remain as close as pos-
past, several expressions have been proposed such as the sible to our set of data, we chose to adopt the following
ones by Burland [4] with IP = 0.73(wL - 20) and Biarez best correlation represented in Fig. 10 by the bold line with
and Hicher [5] with IP = 0.73(wL - 13). Figure 10 pre- a correlation coefficient R2 = 0.9587:
sents the plots of these two parameters for the clays IP ¼ 0:8381wL 16:438 ð13Þ
Cαe
Cαe
0.02 0.02 0.04
0 0 0
0 10 20 30 40 50 0 20 40 60 0 20 40 60 80 100
w (%) w (%) w (%)
Cαe
Cαe
0 0 0
0 10 20 30 40 50 0 50 100 0 20 40 60 80
w (%) w (%) w (%)
(g) (h) (i)
0.04 Vanttila clay 0.04 Murro clay
0.04
Experimental Experimental
Experimental
0.03 Theoretical 0.03 Theoretical HKMC
0.03 Theoretical
Experimental
Zhoushan clay
Theoretical
Cαe
Cαe
0.02 0.02
Cαe
0.02 Experimental
Kaolin
Theoretical
0 0 0
0 20 40 60 80 100 0 20 40 60 80 0 20 40 60
w (%) w (%) w (%)
Fig. 11 Comparison of measured and estimated values of Cae for reconstituted clays
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0.05
Cae ¼ ð0:0007wL 0:0223Þðw=wL Þ0:014978wL 0:23031 ð14Þ
wL = 90% Figure 11 shows the comparison between experimental
0.04 and predicted results estimated by Eq. (14) for all the
selected clays. Despite there are some discrepancies
0.03
between measured and estimated values, Eq. (14)
generally describes the evolution of Cae for reconstituted
Cαe
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Fig. 13 Comparison of measured and estimated values of Cae for intact clays
(a) (b)
2
3 Wenzhou clay (2) Experiment
Vanttila clay Experiment
Predicted Predicted
Cαe=CαeL=0.043 Cαe=CαeL=0.026
2.5
1.5
Void ratio, e
Void ratio, e
1 0.5
1 10 100 1000 10000 1 10 100 1000
Time (h) Time (h)
Fig. 14 Comparison of measured and computed void ratio versus time on two intact clays
increases. Based on these results, a simple nonlinear creep the bonding ratio with an additional parameter n, leading to
formulation was adopted with an additional parameter of a nonlinear creep formulation accounting for soil structure.
nonlinearity m. For simplification and practical use, CaeL The proposed formulation of Cae for intact clays con-
(corresponding to the liquid limit) and CaeP (corresponding tains five material constants CaeL, CaeP, m, n and q0, which
to the plastic limit) were suggested as the reference Cae. can be determined in a straightforward way from conven-
The bond degradation process during straining exerts a tional oedometer testing. Furthermore, correlations
significant influence on the values of Cae. The significant between these material parameters and Atterberg limits
difference of Cae between intact and reconstituted clays were proposed based on available data. By expressing the
was analyzed. The ratio of Cae between intact clay and the material constants as functions of the liquid limit and the
corresponding value for reconstituted clay was related to plasticity index, we are able to suggest a practical
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Acknowledgments We acknowledge with gratitude the financial pression and consolidation of clayey soils is–Hiroshima, Japan,
support provided by the National Natural Science Foundation of pp 537–542
China (Grant No. 41372285), the Fundamental Research Funds for 22. Nash DFT, Sills GC, Davison LR (1992) One-dimensional con-
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