Test Materials and Protocol
- (1)
Test Materials
The high-water-content dredged sludge used in this study was collected from the dredging project site at Jingyue Lake, Zhongxiang City, and Hubei Province, China, exhibiting a grayish black appearance. After retrieval, the fundamental physical property indices of the sludge were determined in accordance with the “Standard for Soil Test Methods” (GB/T 50123-2019) [
17], with the specific measurement results presented in
Table 1. The analysis of the test results identified the Zhongxiang sludge as high-liquid-limit clay (CH). Furthermore, particle size analysis of the Zhongxiang sludge samples was conducted using a laser particle size analyzer reveals that the Zhongxiang sludge samples contain clay particles (diameter < 0.005 mm): 44.88%, silt particles (diameter 0.005–0.075 mm): 54.80%, and sand particles (diameter > 0.075 mm): 0.32%.
The composite curing agent is uniformly mixed and prepared at a mass ratio of 1:1 using ordinary Portland cement (OPC) and ground granulated blast furnace slag (GGBS) as shown in
Table 2. The composite flocculant used consists of the inorganic flocculant quicklime (CaO) and the organic polymer flocculant anionic polyacrylamide (APAM).
- (2)
Sample Preparation Method
To ensure the quality control of the specimens, the following sample preparation procedures shall be strictly followed, where the materials and apparatus used are shown in
Figure 1:
a. Preparation of fluid mud slurry: Based on the measured natural water content of the fluid mud, calculate the required water content of the fluid mud slurry for specimens with the specified equivalent water content using Equation (1) below. Then, determine the additional amount of water to be added to the original mud accordingly. Subsequently, process the mixture using a specific mixing procedure (1 min manual stirring + 5 min mechanical stirring at 120 r/min) to obtain the fluid mud slurry meeting the required water content (as
Figure 2a shows).
In the equation,
m is the mass of water to be added for preparing the fluid mud slurry (g), and
mM is the mass of the fluid mud (g), which can be weighed according to the following experimental requirements:
w is the water content of the fluid mud (%), measured as 110%;
W is the equivalent initial water content (%);
mwAPAM is the mass of water required for preparing the APAM solution (g), with its specific value given in Equation (2).
b. Incorporation of Cement-GGBS Composite Binder: First, accurately weigh ground granulated blast furnace slag (GGBS) and ordinary Portland cement (OPC) according to the predetermined binder dosage. Subsequently, rapidly transfer both materials into a beaker and homogenize using glass rod manual mixing to obtain a uniform cement-GGBS composite binder. Add the composite binder into the fluid mud slurry prepared in Step a, then execute a specified mixing sequence (1 min mechanical mixing at 120 rpm + 1 min manual mixing + 5 min mechanical mixing at 120 rpm) to produce a homogeneous binder–mud slurry mixture (as
Figure 2b shows).
c. Flocculant Addition: Prepare a 0.2% anionic polyacrylamide (APAM) solution by dissolving APAM powder completely using a 2.5 L mini mixer at 120 rpm for 30–60 min. Precisely weigh the required masses of CaO particles and APAM solution, then gradually introduce them into the binder–mud slurry mixture from Step 5. Employ the 2.5 L mini mixer (60 rpm) for 3–4 min until clearly visible macro-flocs form, at which point mixing is immediately terminated. The resulting product constitutes a homogenized flocculant-binder–mud slurry system (as
Figure 2c,d shows).
In the equation,
mwAPAM is the mass of water required for preparing the anionic polyacrylamide (APAM) solution (g);
mM is the mass of the fluid mud (g);
w is the water content of the fluid mud (%), taken as 110%;
WF is the dosage of APAM (%), taken as 0.125%.
d. Using a sample preparation method similar to consolidation testing, the mixed slurry is slowly poured into the cutting ring of the low-pressure consolidometer while being vibrated. It is then placed into a laboratory-customized low-pressure consolidometer for stepwise preloading and curing to obtain the specimen required for permeability testing.
e. Finally, the constant-head permeability test is conducted using the TKA-STC series fully automatic permeameter–consolidometer (as shown in
Figure 3), which consists of a confining pressure permeation line, back-pressure seepage line, permeameter cell, base plate, loading rod, confining pressure valve, and back-pressure valve, to determine the permeability coefficient of the specimen.
During the permeability test, the pressure difference between the permeation pressure and back pressure was set at 20 kPa, thus yielding the calculation formula for the specimen’s permeability coefficient:
In the formula,
k= permeability coefficient (m/s);
Q = seepage flow volume during time t (m3);
L = seepage path length (i.e., specimen height) (m);
t = seepage duration (s).
Three experimental groups (A, B, and C) were established, comprising a total of 36 test conditions. The specific parameters are summarized in
Table 3:
Group A: Binder dosage levels of 7.5%, 10%, 12.5%, and 15%;
Group B: Equivalent initial water content values of 120%, 150%, 180%, and 210%;
Group C: Preconsolidation pressure settings of 30 kPa, 60 kPa, and 90 kPa.
All three groups shared the same curing time conditions (6 h, 24 h, 48 h, and 72 h) as the common controlled variable.