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Article history: A design method for an anti-ice and antiskid wear layer on pavement is presented in this paper. A kind of
Received 8 September 2020 bonding material with excellent properties has been developed that can maintain a good bonding ability
Received in revised form 28 December 2020 in high and low temperature environments and has good UV aging resistance. Porous high-strength shale
Accepted 12 February 2021
aggregates are used to replace portions of stone, and the functional characteristics of the ice inhibition of
Available online 24 February 2021
the wear layer are realized by soaking in saturated salt water. The results show that after adding ceram-
site, the freezing point of pavement can be reduced by approximately 5 °C at most and the ice melting
Keywords:
rate can be increased by approximately 30%. After continuous soaking for ten days, salt can still be pre-
Road engineering
Wear layer
cipitated from the aggregate, which can inhibit the formation of an ice film to a certain extent. As the pro-
Anti-ice portion of ceramsite increases, the polishing resistance of the pavement increases. Under conditions of
Antiskid flooding and freezing, the BPN of the aggregate mixed with ceramsite is approximately 50% higher than
Ceramsite that of andesite aggregate. The wear layer can provide a good anti-ice and antiskid performance, which is
Bonding material helpful for traffic safety under wintry conditions.
Ó 2021 Elsevier Ltd. All rights reserved.
1. Introduction tions are still among the main causes of traffic accidents [4–6].
Therefore, scholars have carried out systematic and extensive
Road transportation is a complex system that integrates research on ice and snow problems on roads.
humans, vehicles, roads, and the environment. With more in- At present, there are two kinds of technical methods to solve
depth research, people are paying more attention to travel quality the problem of ice and snow on the road surface, passive snow
and safety, especially travel under adverse conditions, such as ice, removal technology and active snow removal technology. Passive
snow, rain, and fog, and changeable extreme temperature condi- snow removal technology includes seeding snow melting agents
tions [1,2]. More than 80% of China is affected by freezing and snow and gravel and manual and mechanical snow removal [7,8]. Among
conditions. Ice on roads reduces the friction coefficient, which them, deicing agents are among the most commonly used snow
greatly increases the probability of traffic accidents [3]. Many removal methods because of their low price and convenience.
countries around the world invest significant manpower, material However, corrosion and pollution are big drawbacks of deicing
and financial resources every year to deal with the negative agents [9,10]. Seeding gravel not only improves the skid resistance
impacts of ice and snow hazards. However, ice and snow condi- of pavement but is also easy to clean; however, it seriously affects
driving comfort. Manual snow removal and mechanical snow
⇑ Corresponding authors. removal are very expensive, and ice in pavement gaps is not easy
E-mail addresses: yijunyan@hit.edu.cn (J. Yi), fengdecheng@hit.edu.cn (D. Feng).
to remove, which also causes safety hazards.
https://doi.org/10.1016/j.conbuildmat.2021.122734
0950-0618/Ó 2021 Elsevier Ltd. All rights reserved.
Z. Pei, J. Yi, Y. Li et al. Construction and Building Materials 282 (2021) 122734
Active snow removal technology is gradually developing. The which will allow it to withstand erosion due to the driving load and
use of heat pipe methods, microwave heating methods, infrared natural conditions on the surface of the road. Ceramsite material
heating methods, and conductive concrete methods can be used which can be prepared from shale or shale soil through the method
to eliminate ice and snow through energy transformation [11– of granulation meets the above requirements, so it is a good choice
13]. These technologies are mainly applied in airport pavements for the aggregate [23–25]. At present, the reserves of shale and
and have achieved good results. However, it is difficult to imple- shale soil are relatively rich, and with the upgrading of production
ment these methods because they require special construction, technology and equipment, the price of ceramsite is also decreas-
and is not suitable for large-scale use in highway engineering ing year by year, generally 400–550 RMB per ton. Besides, because
[14,15]. The coating method is to spread hydrophobic materials of the environmental policy, there are fewer and fewer high-
on the road surface to increase the contact angle between water quality stones available for roads in China, especially for the road
molecules and surface materials, which not only prevents water surface. In many areas, the price of stone for pavement has
from penetrating into pavement gaps but also prevents surface increased 3–5 times, reaching 300–500 RMB per ton. The price of
moisture from accumulating and condensing into ice [16,17]. How- ceramsite is close to the price of high-quality stone, and the use
ever, the coating method may affect the lateral friction coefficient of ceramsite in road engineering will not have a great impact on
of pavement under normal conditions. Self stress snow removal the project cost.
pavement adds elastic materials, such as rubber particles, into However, only using ceramsite as the aggregate does not meet
pavement materials and makes use of the large deformation capac- the requirements of pavement performance, so it is necessary to
ity of these elastic materials to promote the impact of the traffic use a mixture of ceramsite and ordinary stone.
load to break ice and snow and to inhibit the formation of snow
and ice on the road surface [18]. The durability of this technology
requires further verification. Salt storage type pavement is a tech- 2.1.1. Ceramsite
nology that involves storing salt or anti-ice components in pave- The ceramsite used in this paper was produced in Henan Pro-
ment materials via special processing that is slowly released vince, China, and is a high strength shale gravel ceramsite. The
when encountering snow and ice water [19,20]. This technology technical indicators of the ceramsite were tested following a Chi-
has achieved good results and has good reference significance nese Specification-Lightweight aggregates and its test methods
and promotion prospects. (GB/T 17431.2-2010). The indicators are shown in Table 1.
On the other hand, with the increase of highway service life, an
increasingly number of highway surface functions are lost. Cracks
not only weaken driving comfort but also promote the entry of 2.1.2. Stone material
moisture into the pavement structure and aggravate pavement Commonly used andesite was used in conjunction with ceram-
damage. At the same time, a decrease in the skid resistance perfor- site. In the surface treatment and seal structure of the pavement,
mance of the road surface also seriously threatens driving safety stone with a diameter of 4.75–9.5 mm (S12) is the most widely
performance. Using a thin wearing layer can increase the friction used. Therefore, this paper chose 4.75–9.5 mm andesite rock mate-
force of pavement, improve the seepage condition of pavement rial to carry out the experiment. The properties of andesite are
and prolong the service life of pavement [21,22]. Therefore, the shown in Table 2.
thin wearing layer technology has become more widely used in
pavement maintenance engineering. In higher latitude areas, if
snow removal technology and a thin wearing layer can be com- 2.1.3. Design scheme of the aggregate
bined, a new anti-ice and antiskid wear layer structure can be The crushing value and abrasion value are the main technical
developed. At the same time, pavement maintenance can reduce indexes used to evaluate the performance of the aggregate. The
the effects of ice and snow on pavement performance to improve mass ratio of ceramsite and andesite was taken as a variable. The
road service life and traffic safety. crushing value and abrasion value were tested following a Chinese
In this context, a design method for the anti-icing and antiskid Specification (JTG E42-2005). The results are presented in Figs. 1
wear layer is proposed in this study. A kind of bonding material and 2. According to the Chinese Specification (JTG F40-2004), the
with excellent properties was prepared by a specific process. Light- aggregate crushing value and abrasion value of the surface of a
weight and high-strength ceramsite was used to replace a portion high-grade highway should not be <26% and 28%, and that of other
of stone, and the aggregate was soaked in saturated sodium chlo- grade highway should not be<30% and 35%. To ensure good perfor-
ride solution to store salt in the pores of the aggregate. Pull-off mance of the aggregate, according to the crushing value and abra-
tests, UV aging tests, wheel type polishing tests, indoor ice melting sion value, a preliminary formulation for the aggregate ratio is
tests, and salting-out tests were designed to evaluate the durabil- shown in Table 3.
ity, skid resistance and ice removal performance of the anti-ice and
antiskid wear layer. The purpose of this study is to put forward a
new type of antiskid and anti-ice pavement functional layer that
Table 1
is easy to build and maintain and provides a new idea for ice
Technical indexes of ceramsite.
removal and maintenance in pavement engineering.
Technical indexes Measured Criteria Testing method
value
Table 2 Table 3
Technical indexes of andesite. Ratio of the aggregates.
Technical indexes Measured value Criteria (High- Testing Test groups Mass ratio (ceramsite: andesite)
(4.75–9.5 mm) grade highway) method
A 100% ceramsite
Surface layer
B 1:0.5
Apparent relative 2.783 2.60 JTG E42- C 1:1
density (kg/m3) 2005-T 0304 D 1:2
Water absorption 1.30 2.0 JTG E42- E 1:3
(%) 2005-T 0304 F 100% andesite
Crushing value (%) 12.56 26 JTG E42-
2005-T 0316
Los Angeles 15.3 28 JTG E42-
abrasion value 2005-T 0317 only maintain a good bonding performance in a low temperature
(%) environment but should also have good high temperature resis-
tance. Therefore, a material that can ensure a good bonding perfor-
mance in high and low temperature environments is needed to
50 bond the aggregate firmly to the road surface. The resin asphalt
seems to have a good bonding performance and is widely used in
bridge deck pavement engineering [26,27]. However, it has not
40.51
been widely used in road engineering. One of the main reasons is
40
that the cost of resin asphalt is high. Besides, the quality of resin
asphalt materials available on the market is uneven. Considering
Crushing Value (%)
30.61 the cost and technical requirements of the wearing layer, a kind
30 of bonding material suitable for wear layers was developed in this
23.85 paper.
20.99
20 18.01
2.2.1. Asphalt
12.56 Base asphalt (90#) is used as the basic material, and its techni-
10 cal indicators are shown in Table 4.
30
2.2.4. Maleic anhydride
24.1 In previous studies on the chemical modification of asphalt,
Abrasion Value (%)
25
maleic anhydride has attracted much attention as an important
20.6 reagent. Maleic anhydride can react with asphalt and directly
20 improve the compatibility between asphalt and resin. Maleic anhy-
15.3 dride contains a carbon–carbon double bond that can participate in
15 free radical reactions. Carbon-carbon double bonds can be added to
asphalt molecules at high temperature, allowing maleic anhydride
10 to be grafted to one end of asphalt molecules. As for the reaction
mechanism, the industry agrees that the Dies-Alder reaction is
5 involved [28]. In the follow-up reaction, asphalt is not only filled
with epoxy resin as a filler but is also involved in the curing process
of epoxy resin as a reactant, which helps to improve the compati-
0
1:0 1:1 1:2 0:1 bility of post-reaction resin asphalt systems. At the same, the addi-
Ceramsite:Andesite (Mass Ratio) tion of maleic anhydride to asphalt reduces the elongation at break
of the material, so the amount of maleic anhydride used should not
Fig. 2. Abrasion value of the aggregate. be excessively high.
Previous studies have shown that the conversion rate between
asphalt and maleic anhydride for 200 min can reach about 60% at
2.2. Bonding material 160 °C [29]. Therefore, there is a part of the residual maleic anhy-
dride in asphalt. After the full reaction of maleic anhydride with
Modified asphalt is generally used as a bonding material in asphalt, the sample was found to have a large number of white par-
wear layers and sealing layers of pavement. However, the anti- ticles uniformly distributed in asphalt from the SEM image, as
ice and antiskid wear layer studied in this paper is generally used shown in Fig. 3. According to existing research results, the white
in middle and high latitudes, and the bonding material should not particles are free maleic anhydride postreaction [30].
3
Z. Pei, J. Yi, Y. Li et al. Construction and Building Materials 282 (2021) 122734
Table 4
Technical indexes of base asphalt.
Maleic Anhydride
Maleic Anhydride
(a) SEM image of 800 times (b) SEM image of 2400 times (c) SEM image of 8000 times
Fig. 3. SEM images of maleated asphalt.
Table 5
Technical Indexes of SBS-modified Asphalt.
(a) Drawing instrument (b) Test base (c) Drawing anchor head
bonding material was tested after curing at 100 °C for 0.5 h. The 3.2. Ice inhibition tests of the wear layer
temperatures of the drawing test were set to 15 °C, 20 °C, and
60 °C. 90# base asphalt and SBS-modified asphalt were used as 3.2.1. Analysis of the ice inhibition mechanism
the contrast test group. Salt precipitation can reduce the freezing point of a solution,
and colligative properties of solution is the quantitative law
describing this phenomenon. For a dilute solution of nonelec-
trolytes, the freezing point decreases with the increasing molar
3.1.2. Ultraviolet aging test
concentration of the solution, and there is a good positive correla-
The surface of the road is directly exposed to the natural
tion between the decreasing value of the freezing point and the
environment and is most vulnerable to solar radiation. However,
molar concentration of the solution. Ionization of the electrolyte
polymeric materials can easily undergo photochemical reactions
leads to a deviation in the dependence on the concentration of
under UV irradiation, which can significant affect material per-
the solution and does not satisfy the corresponding quantitative
formance. Therefore, the aging resistance of the adhesive mate-
relationship. In this case, the isotonic coefficient is generally intro-
rials was evaluated by using indoor ultraviolet accelerated aging
duced to reflect this deviation [32,33]. The specific calculation
equipment. The instrument was a self-developed ultraviolet
method is shown in formula (1).
aging acceleration device, as shown in Fig. 7 [31]. The ultravio-
let light source used a UVA–340 lamp tube, and the radiation
intensity was 60–70 W/m2, which is approximately three times DT fp ¼ kfp m i ð1Þ
the maximum daily radiation intensity in Harbin. The test tem-
perature was controlled at 60–65 °C, which is equivalent to the
where 4Tfp is the decreasing value of the freezing point; kfp is the
highest temperature of the road surface in summer. 90# base
freezing point decrease constant, which is 1.853 for water; m is
asphalt and SBS-modified asphalt were used as the contrast test
the molar concentration of the solution; and i is the iso-osmotic
group.
coefficient, which is 2 for a sodium chloride solution.
According to the formula, the concentration of sodium chloride
solution needed to reduce the solution of the road surface to the
3.1.3. Fourier transform infrared spectroscopy experiment (FTIR) corresponding freezing point is calculated, and then, the amount
Fourier transform infrared spectroscopy (FTIR) was used to ana- of precipitated salt needed to achieve this effect is calculated.
lyze the microscopic changes of the bonding materials before and Table 6 shows the concentration of the chloride solution required
after UV aging to evaluate the aging resistance of the materials. when the freezing point of the road surface decreases by 5 °C.
5
Z. Pei, J. Yi, Y. Li et al. Construction and Building Materials 282 (2021) 122734
Table 6 (2) The specimen was prepared by the above method and then
Mass concentration of the NaCl solution corresponding to the decrease of the freezing frozen at 10 °C for more than 6 h, allowing it to be com-
point.
pletely frozen. The sample is shown in Fig. 9. The sample
4Tfp (℃) Molar concentration of the Mass concentration of was then placed at 25 °C ± 1 °C around the water-
NaCl solution (molkg1) the NaCl solution (%) absorbing material, allowing the water-absorbing material
0.5 0.130 0.786 to absorb the melted ice water in time. Using five-minute
1 0.270 1.573 time intervals, the sample mass was measured by a high pre-
1.5 0.400 2.359
cision electronic balance, and the ice melting mass at each
2 0.540 3.145
2.5 0.670 3.391 time interval was determined. Then, the cumulative ice
3 0.810 4.718 melting mass percentage was obtained. Based on the cumu-
3.5 0.940 5.504 lative ice melting mass percentage, the ice melting rates of
4 1.080 6.290 the specimens with different aggregate ratios were deter-
4.5 1.210 7.077
5 1.340 7.863
mined. When the first melting cycle was complete, the spec-
imen was dried in an oven, and the second melting cycle test
was carried out according to the above steps. The continuous
ice melting effect of different specimens was evaluated by
3.2.2. Indoor freezing test
the above tests.
To analyze the ice melting performance of the wear layer, a lab-
oratory test was designed to determine the ice inhibition perfor-
mance. To facilitate the smooth progress of the experiment, a 3.2.3. Salt precipitation testing
self-made 10 cm 10 cm pedestal was made, and an wear layer Considering that the wear layer is soaked by ice water and rain
was laid on the pedestal plate. According to the technical standards water during its use, salt will be lost quickly. To determine the salt
of a gravel seal, the amount of cementing material needed was loss of the wear layer under wetting conditions, a salt precipitation
determined to be 1.2–1.3 kg/m2. The aggregate was soaked in a sat- test was designed. The specimen was prepared similar to the spec-
urated sodium chloride solution for 24 h before use and dried. The imen preparation described Section 3.2.2 and was placed in a metal
aggregate was fully mixed according to different mass ratios and vessel of a certain size and completely submerged in 250 mL of dis-
evenly laid on the substrate, and a roller was used to roll the aggre- tilled water. The content of chloride ions in the solution was peri-
gate evenly. Then, the sample was kept at 100 °C for 0.5 h, and the odically monitored using a NCL-AL rapid determination
wear layer was fabricated. instrument, and the quality of sodium chloride that precipitated
from the solution was obtained (the ambient temperature was
(1) First, the specimens were surrounded with custom-made 25 °C ± 1 °C). The test process is shown in Fig. 10.
PVC plastic. Then, 80 mL of distilled water was spread on The NCL-AL chloride ion content analyzer back-calculates the
the surface of each specimen to seal it to prevent leakage, ion concentration according to the potential difference in the solu-
as shown in Fig. 8. The specimens were frozen at 1 °C, tion. NaCl solutions of 0.001 mol/L, 0.01 mol/L, and 0.1 mol/L were
5 °C and 10 °C for 4 h, and the surface freezing of the prepared as calibration solutions, and the calibration solutions
specimens with different aggregate ratios was observed. with different concentrations and corresponding potential differ-
6
Z. Pei, J. Yi, Y. Li et al. Construction and Building Materials 282 (2021) 122734
ences were used to fit the linear relationship between the loga- 3.3.2. Anti sliding performance test
rithm of the concentration and potential difference. Then, the dif- The British Pendulum tester is easy to debug and operate, and
ferent solution concentrations were calculated according to the often used to measure the BPN of the road surface to characterize
potential difference obtained by the test so that the quality of its antisliding performance, as shown in Fig. 12. In this study, the
the sodium chloride precipitated by the test piece during that time sliding resistance of the specimen surface under different condi-
period could be obtained. tions was measured by a British Pendulum tester.
To evaluate the precipitation and change law of the ice-
suppressing salt in the sample, the abovementioned sample was
continuously observed for many days. Two hundred-fifty milliliters 4. Results and discussion
of distilled water was injected every day, the potential difference of
the solution was measured after 24 h of soaking, the chloride ion 4.1. Pull-off test results of bonding materials
concentration of the solution was obtained, and the mass of salt
that precipitated on the test piece that day was calculated. Thus, To verify the bond strength of the homemade material, 90#
the salt change of the wear layer under a continuous immersion base asphalt and SBS-modified asphalt were selected for compar-
environment was obtained. ison, and their pull-off strengths at different temperatures (60 °C,
20 °C and 15 °C) were measured. The results are shown in Fig. 13.
The test data show that 90# base asphalt has the lowest pull-off
3.3. Test of the skid resistance of the wear layer
strength, the SBS-modified asphalt has a good effect, and the
homemade bonding material has the highest pull-off strength.
The antiskid performance of the wear layer in different environ-
The pull-off strength of the homemade bonding material is about
ments is also particularly important to its application. The British
six times higher than that of base asphalt and three times higher
Pendulum Number (BPN) is typically used to characterize the skid
than that of modified asphalt. This results show that the home-
resistance of pavement and can be measured by a British Pendu-
made bonding material has a better bonding performance than
lum tester. In general, newly built pavement can meet the require-
the SBS-modified asphalt in high and low temperature environ-
ments of antiskid technical standards. However, under the
ments, indicating that the aggregate adheres to pavement better
repeated action of a vehicular load, the texture of the road surface
using the homemade bonding material.
aggregate is gradually polished, and the skid resistance of the road
surface decreases. At the same time, in rainy and snowy weather,
the road surface is covered with water film or ice film, which 4.2. UV aging resistance of bonding materials
reduces the skid resistance, threatening traffic safety. In this study,
the antiskid performance of the wear layer was characterized by In the process of using the asphalt mixture, it is affected by
the BPN. ultraviolet aging. Ultraviolet aging not only makes asphalt hard
and brittle but also makes the adhesion between asphalt and the
3.3.1. Wheel polishing test aggregate worse, resulting in the aggregate gradually falling off
The experiment was carried out using the accelerated polishing the road surface. In this paper, the samples to be tested were
system made by the research group. The system was composed of a placed in an accelerated UV aging chamber for 15 consecutive
tire grinder, temperature control device, pressure measurement days. FTIR was used to analyze the materials before and after aging.
and speed regulation device [34]. The polishing instrument and 90# base asphalt and SBS-modified asphalt were selected for com-
test process are shown in Fig. 11. According to the research results parison. The infrared spectral data of the materials before and after
of Xie, under different tire pressures, the long-term antiskid perfor- the aging test are shown in Figs. 14–16.
mance of road surfaces first decreases and then tends to gradually For 90# base asphalt, after UV aging, a carbonyl group (C@O)
stabilize, and the stable final value has little difference. According was produced at 1703 cm1 and the aromatic ring (C@C) vibration
to past experience using the instrument, the tire ground pressure was enhanced at 1602 cm1. The absorption peak of ACH2-O-CH2-
was 0.2 MPa, the amount of spraying water was 35 ± 5 mL/min, was observed at 1150–1060 cm1, which tended to increase after
and the dosage of carborundum was 8 ± 2 g/min. The size of the aging. The hydrogen bond absorption band also increased at
specimen was 30 cm 30 cm, and the specimen was prepared 3200–3500 cm1. The CAH stretching vibration at 2922 cm1
according to the abovementioned method. The experiment was and 2856 cm1 decreased after asphalt aging.
carried out at 20 °C ± 1 °C, and the specimen was polished at a For SBS-modified asphalt, after UV aging, the carbonyl group
speed of 60 times/min. The pendulum value of the specimen was (C@O) increased at 1700 cm1, the aromatic ring (C@C) vibration
regularly measured to analyze the attenuation of the surface skid increased at 1601 cm1, and the hydrogen bond absorption band
resistance of the specimen. at 3200–3500 cm1 also increased, which were similar to that of
7
Z. Pei, J. Yi, Y. Li et al. Construction and Building Materials 282 (2021) 122734
than the other materials, and its UV aging resistance was relatively
more stable.
15
11.65 4.3.2. Results of ice melting test
80 mL of distilled water was evenly spread on the surface of the
10 specimen, and then, the specimen was frozen at 10 °C for more
6.91 than 6 h and was taken out after being completely frozen. The
5.92 specimen was melted at 25 °C ± 1 °C, placed around the absorbent
4.75 material, and weighed in five-minute intervals, and the amount of
5
2.73 melted ice was calculated.
1.91 During the first ice melting cycle, the cumulative ice melting
0.71 mass percentage of the specimen is shown in Fig. 17. The ice melt-
0 ing rate of the specimen with ceramsite was faster than the spec-
Homemade Material SBS 90 # imens without ceramsite. It took approximately 70 min to
complete the first cycle of ice melting for the F group (andesites).
Fig. 13. Pull off test results at different temperatures.
However, in group A (ceramsite), the melting time was approxi-
mately 45 min, and the ice melting rate of group A was 33% higher
than that of group F. With decreasing ceramsite content, the ice
90# asphalt. In addition, the sulfoxide group (S@O) significantly melting rate decreased. The ice melting effect of groups with cer-
increased at 1030 cm1. amsite was better than that of group F.
For the homemade bonding material, the carbonyl group (C@O) At the end of the first cycle, the specimen was dried and the sec-
increased at 1698 cm1 after UV aging, and the CAH stretching ond ice melting cycle was tested according to the same procedure.
vibrations at 2922 cm1 and 2856 cm1 decreased after aging. The test results are shown in Fig. 18. The ice melting data of each
The vibration absorption peak of a methyl group at 1454 cm1 group in the second cycle were similar to those in the first cycle.
was weakened, and the aromatic ring at 722 cm1 was decreased. Comparing the two groups of ice melting data (seen in Fig. 19),
However, these trends were relatively weak. the ice melting rate in the second ice melting cycle slightly
The infrared spectra of the homemade bonding material and decreased, and the ice melting time of group A was extended to
SBS-modified asphalt had specific peaks. Before and after UV aging, 50 min. The ice melting rates of the other groups slightly
the three kinds of bonding materials had similar trends and unique decreased, and the total ice melting time was not extended. The
characteristics [35,36]. In general, after UV aging, the spectrum of ice melting rate of group A was 28% higher than that of group F.
the homemade bonding material had a smaller changing trend And the ice melting effect of other groups was better than that of
8
Z. Pei, J. Yi, Y. Li et al. Construction and Building Materials 282 (2021) 122734
105
100
3335
Transmittance (%) 95
1069
718
747
869
1703
812
1602
90
1377
85
1455
80
2855
75
70
65 Virgin
2922
60 Aged
4000 3500 3000 2500 2000 1500 1000 500
-1
Wave Number (cm )
Fig. 14. Infrared spectra of 90# base asphalt before and after UV aging.
100
3261
Transmittance (%)
80
1700
1601
60
1030
1304
965
698
860
812
722
747
1373
40
Virgin
1455
2922
2855
20 Aged
Fig. 15. Infrared spectra of SBS-modified asphalt before and after UV aging.
100
1698
Transmittance (%)
90
1605
694
1374
80
722
1207
1180
2855
1454
1505
1243
70
825
2922
60
Virgin
Aged
4000 3500 3000 2500 2000 1500 1000 500
-1
Wave Number (cm )
Fig. 16. Infrared spectra of the homemade bonding material before and after UV aging.
Table 7
Results of the freezing test.
9
Z. Pei, J. Yi, Y. Li et al. Construction and Building Materials 282 (2021) 122734
100
A on ice melting.
B Then, five ice melting tests were carried out on groups A and F.
80
C It was found that the complete ice melting time of group A was
70 min
D approximately 50 min and the complete ice melting time of group
E F was approximately 70 min, and the ice melting capacity did not
60 F
significantly decrease. As the function of ice suppression mainly
comes from the salt stored in the aggregate, to further analyze
45 min
the attenuation of the ice suppression performance of wearing
40
with time, salt precipitation test analysis of wear layer is carried
out in next section.
20
4.4. Test results of salt precipitation
100
A cipitation also increased. Group A had the largest amount of
B sodium chloride. In all groups, the salting out amount was most
80 C significant in the first hour and then tended to stabilize. According
70 min
milliliters of distilled water was injected every day, and the chlo-
40
ride ion concentration of the solution was measured after soaking
for 24 h. The mass of salt that precipitated out of the test piece was
obtained, and the results are shown in Fig. 21.
20
It can be seen from the figure that the salt loss of the test groups
mixed with ceramsite was large during the first two days of
0 immersion, but from the third day on, the quality of salt precipi-
tated daily gradually reached a stable level. From the eighth day
0 10 20 30 40 50 60 70
on, the quality of daily salt precipitation was basically stable,
Time (min)
approximately 0.05–0.06 g. Considering the size effect of the spec-
Fig. 18. Change in the ice melting mass with time in the second cycle. imen, in this case, approximately 5–6 g of salt will be precipitated
every day when converted into 1 m2 specimens. It is assumed that
the thickness of the ice film is 0.1 mm at the beginning of ice for-
mation [37,38]. Referring to the mass concentration in Table 6, the
salt that precipitated from the specimen can reduce the ice film
Cumulative mass percentage of ice melting (%)
100
A1 formation temperature on the aggregate surface to approximately
A2 4 °C. In this case, It is suitable for the area where the road surface
C1 is easy to produce thin ice and dark ice.
80
70 min
C2
F1 4.5. Analysis of the antisliding performance of the wear layer
50 min
60 F2
4.5.1. Results of the antisliding performance after polishing
45 min
10
Z. Pei, J. Yi, Y. Li et al. Construction and Building Materials 282 (2021) 122734
0.9
0.4
0.3
0.2
0.1
0.0
-0.1
0 1 2 3 4 5 6
Time (h)
Fig. 20. Accumulated salting out quality on the first day.
Mass of accumulated precipitated salt (g)
0.8 A
0.7 B
C
0.6 D
0.5 E
F
0.4
0.3
0.2
0.1
0.0
1 2 3 4 5 6 7 8 9 10
Day
Fig. 21. Daily salt precipitation.
Table 8
The BPN under different polishing times.
Times (min) Polishing times A (100% ceramsite) C (1:1) D (1:2) E (1:3) F (100% andesite)
0 0 67 69 63 65 68
10 600 66 66 62 64 66
20 1200 65 65 61 62 64
30 1800 65 64 61 59 63
40 2400 64 62 60 58 61
50 3000 63 61 59 57 60
60 3600 63 60 59 55 58
80 4800 62 60 58 56 56
100 6000 62 59 58 56 55
120 7200 62 59 57 56 54
y ¼ A eBx þ C ð2Þ F showed a downward trend. During the test, the inner pores of
ceramsite were gradually exposed after wear, which improved
It can be seen from the chart that the BPN decay of group A was
the antisliding performance. Therefore, after adding ceramsite,
the slowest. Group F had a higher BPN when it was not polished,
the wheel burnishing resistance of the specimen was improved,
but the BPN decayed fastest in the test process. Among them, the
which helped improve the antisliding performance of the test piece
BPN of groups A and C were always larger than that of group F.
in the middle and later periods.
However, in groups D and E, the BPN were less than that in group
F at the initial stage. With increasing polishing time, the amplitude
of the BPN attenuation was less than that of group F, and after 4.5.2. Results of antisliding performance under different environmental
reaching a certain number of polishings, the BPN exceeded that conditions
of group F. In general, after 7200 polishing tests, the BPN of groups Due to the effects of rain, ice and snow during use, the road sur-
A, C, D, and E gradually tended to be stable, while the BPN of group face will become increasingly wet and slippery, and its antisliding
11
Z. Pei, J. Yi, Y. Li et al. Construction and Building Materials 282 (2021) 122734
70
A: y=5.89×e-3.30x+61.18, R2=0.9674
68 C: y=10.62×e-4.24x+58.30, R2=0.9803
D: y=7.13×e-2.32x+55.84, R2=0.9749
66 E: y=10.85×e-5.23x+55.06, R2=0.9234
Pendulum Value (BPN) F: y=18.97×e-1.98x+49.17, R2=0.9936
64
62
60
58
56
54
performance will decline, which will lead to potential safety haz- is approximately 40% higher than that of group F. This finding
ards. Therefore, four groups of antisliding tests under different shows that the antisliding performance of the road surface can
influencing factors were designed. Due to the small amount of cer- be improved by adding ceramsite in bad environments.
amsite in Group E, its anti-ice performance was not as obvious as
that of Groups C and D. Group A, C, D, and F specimens were 5. Analysis and recommendations on the field applications of
selected for subsequent tests. First, 30 cm 30 cm specimens were the wear layer
prepared. Then, a specimens was immersed in a water tank and
removed immediately after wetting as the specimen under the 5.1. Construction time
normal temperature wetting condition. The specimens were
soaked in the pool for 1 h and then removed as the specimens For the homemade bonding material, there is curing reaction in
under the normal temperature immersion condition. After soaking the use process, so the main index to be investigated is its dry time.
in the water tank for 1 h, the specimens were placed into refriger- Dry time refers to the initial solidification of the bonding material,
ators at 5 °C and 10 °C for more than 4 h and removed as the loss of fluidity and initial solidification of the surface. Table 10
specimens under freezing conditions. The specimens under the dif- shows the drying time of the homemade bonding material. It is
ferent conditions were tested at 20 ± 1 °C to analyze the skid resis- suggested that the temperature should not be lower than 20 °C
tance of pavement. The test results are shown in Table 9. when using the bonding material. If the temperature is too high,
It can be seen from the table that the BPN of every group were it is necessary to strictly control the construction time and reason-
similar under the different wetting conditions. With the gradual ably arrange the construction process. The construction of the wear
deterioration of the environment, the BPN undergo different layer mainly refers to the requirements of the sealing coat. The
degrees of decline, and the reduction of the BPN of F group is the method of on-site rapid construction is mainly adopted, using ded-
largest. Under immersion, the BPN of group A almost did not icated synchronous gravel sealers, road rollers, and loaders. After
decrease, while that of group F decreased significantly. The reason spreading the asphalt binder and crushed stone, road rollers are
is that there are many pores in ceramsite and some water is used to stabilize the pressure in time, which not only ensures that
absorbed into the pores, so the influence of water on the antisliding there is enough time for on-site construction but also enables the
performance is weakened in group A. At 5 °C, the BPN of group A wear layer to achieve better performance effects.
is approximately 50% higher than that of group F. Because the spec-
imens of group A are not frozen, B and C are partially frozen, and 5.2. Aggregate ratio
group F is completely frozen, there are significant difference of
the BPN among the groups. Additionally, at 10 °C, the surfaces According to the analysis of performance of the wear layer, it is
of the four groups of specimens are completely frozen, so the suggested that the mass ratio of ceramsite to andesite should be
BPN are greatly reduced. However, the specimen with ceramsite set between 1:1 and 1:2. The stone is not limited to andesite,
is still much higher than that of group F, and the BPN of group A and limestone, basalt and so on can be used. If the stone have high
Table 9
BPN under different conditions.
12
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Z. Pei, J. Yi, Y. Li et al. Construction and Building Materials 282 (2021) 122734
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