2.1. Sample Preparation and Experimental Design
The sample selected in this experiment is from an in-service cross-river tunnel segment, whose designed strength grade is C50, 28-day compressive strength is 61.6 MPa, and water–cement ratio is 0.4. The concrete is made of P.O 42.5 grade ordinary Portland cement with 28-day flexural strength of 7.5 MPa and compressive strength of 46.8 MPa. Fly ash for use in concrete application specification GB/T 1956-2017 was Class F-II fly ash, with fineness of 45 μm sieve and residue 15.2%. The specific mix ratio parameters are shown in
Table 1.
The steel bar was extracted after the segment was broken, and the cylinder sample of 50 mm × 100 mm was extracted and cut using the core drilling equipment. At the beginning of the test, the sample age was 1150 d, and the original compressive strength was 75 MPa.
Before the original tunnel segments were put into use, isooctyltrioxyethylsilane was used to spray protective coating on the surface of the segments, and the designed dosage on site was 450 g/m2.
In this paper, the samples were divided into protected group, exposed group and control group. Before the experiment, the protection group was coated with silane coating according to the designed dosage, and the amount of brushing for a single sample was 8.9 g. The surfaces of the exposed group and the control group were not treated.
The curing cycle of dry and wet cycle experiment consisted of a soaking stage (wet stage) and a drying stage (dry stage), and the curing starts from the soaking stage. The erosion process of tunnel segments was simulated by soaking the test blocks in the erosion solution of corresponding components during the experimental soaking period. At the soaking stage, the test blocks of the protection group and the exposure group were placed upright in a PVC box with a lid containing 10% sodium sulfate solution, and the control group was placed in a PVC box also containing water. The distance between the top of the test block and the liquid level in the box was no less than 3 cm, and the solution in the box was replaced every 30 cycles. PVC box was placed in constant temperature and humidity curing box, with setting curing temperature of 20 ± 0.5 °C and relative humidity of 95 ± 0.5%. After soaking the samples for the specified time, they entered the drying stage. The samples were removed from the erosive liquid tank, the residual liquid on the surface was wiped off, and then they were placed in the blast drying oven. After being dried at 60 °C for 6 h, the samples were taken out and cooled in a cool and ventilated place for 2 h and then put back into the original PVC box for the next wetting and drying cycle. Three groups of samples began a cycle at the same time, with each group of samples undergoing cycles 180 times. The sample preparation and curing process are shown in
Figure 1. The specific conservation environmental parameters of each group are shown in
Table 2.
2.3. Ultrasonic Velocity Test and Data Calculation
Starting with the dry and wet cyclic erosion experiment, ultrasonic velocity was tested once every 20 times after dry and wet cyclic curing. Before the test, it was necessary to arrange measuring points for the sample. Based on the base position of the sample, 4 acoustic measuring surfaces H1, H2, H3 and H4 were arranged at equal intervals of 2 cm upward. A position on the H1 interview sample was selected as the starting point M11 of H1 acoustic surface measurement, and the measurement points M12, M13, …, M118 were arranged in the side circumferential direction with equal intervals of 20° in a clockwise direction.
The measuring line with M
11 as the measuring point was denoted as L
1, and so on; nine measuring lines were arranged in a clockwise direction. The starting points M
21, M
31 and M
41 of other acoustic measuring surfaces were marked at the same vertical position as M
11, and the remaining measuring points H
2, H
3, and H
4 were arranged according to the same rules as H
1 and marked with oil pen. The arrangement of measuring points and the testing process are shown in
Figure 3.
After marking the test points of the samples, the initial sound velocity was tested one by one for each group of samples. During the test, H1, H2, H3 and H4 acoustic surfaces were used for sound velocity test layer by layer. Before testing the ultrasonic velocity of the measuring point, apply an appropriate amount of coupling agent on the surface of the measuring point of the sample and the surface of the measuring probe, and align the center of the transducer with the measuring point. Test from Mi1, and measure the waveform of sound wave passing through the sample in a clockwise direction. The transmitting transducer moves from Mi1 to Mi9 one by one in a clockwise direction, while the receiving transducer moves from Mi10 to Mi18 one by one in a clockwise direction. Each time the two transducers move, a test is conducted accordingly, and the test velocity is calculated. After the test is completed, the residual coupler on the surface should be cleaned with a wet towel, and the samples should be cleaned with the corresponding soaking solution of each group to restore the curing environment on the surface of the samples.
In this paper, the sound velocity test of test measuring line on measuring surface for the times is denoted as .
Then, the average sound velocity of surface
in
times test can be calculated according to Formula (1):
The average sound velocity of the first test sample
can be calculated according to Formula (2):
In order to analyze the change of velocity of the sample in the wet and dry cycle, the average ultrasonic velocity change rate
of the sample is defined according to Formula (3):
In order to analyze the fluctuation of ultrasonic velocity at each measuring point in the dry–wet cyclic erosion experiment, the change rate of ultrasonic velocity
at a single point is defined to be calculated according to Formula (4):
where
represents the change of the ultrasonic velocity relative to the original ultrasonic velocity of the sample located on the measuring line
of the measuring surface
after the first test.
In general, the dynamic elastic modulus
of materials can be calculated using Formula (5), where
is the longitudinal ultrasonic velocity of materials,
is the Poisson’s ratio of materials, and
is the density of materials:
If the coefficient
is:
then Formula (5) is:
According to Formula (7), the dynamic elastic modulus of materials can be changed by the longitudinal ultrasonic velocity of materials and specific material parameters.
When analyzing the overall dynamic elastic modulus of the sample, the average velocity
is used in this paper, so Formula (7) is:
Namely, is the dynamic elastic modulus of the sample under n times of loading.
In the process of erosion, due to the constant change of
of the sample, its
changes accordingly. For comparative analysis of its damage process, the damage metric of the dynamic elastic modulus
is defined as:
where
is the dynamic elastic modulus of the sample before the dry and wet cyclic erosion, i.e., the initial dynamic elastic modulus.
As can be seen from Formulas (8) and (9), although is a measure of the change of dynamic elastic modulus in the process of cyclic dry–wet erosion, its result is not affected by the material characteristics of the sample. When the sample is filled in the early stage of erosion, the dynamic elastic modulus increases, and is negative. When the sample deteriorates due to subsequent damage, the dynamic elastic modulus decreases, and is positive.