Performance of Cement Paste with Denitrified Fly Ash Containing NH4HSO4

The denitrification process was completed in coal-fired power plants, resulting in the fly ash containing NH4HSO4. When this kind of fly ash with ammonia was applied to cement and concrete, there could be phenomena such as a retarded setting time, decreased compressive strength, and volume expansion. This paper mainly investigated the influence of fly ash containing NH4HSO4 on the properties of fly ash cement paste, and pastes with NaHSO4 were set as the control samples. The research on Na+ in cement hydration was studied. The influence of NH4HSO4 content in fly ash on the properties of fly ash cement paste was also investigated. It was found that NH4+ could greatly affect the properties of fly ash cement paste, such as significantly reducing the fluidity, prolonging the setting time, decreasing the compressive strength, increasing the drying shrinkage, decreasing the total heat released during the hydration, and affecting the content of calcium hydroxide hydrate. Increasing the ammonia content of the denitrified fly ash would reduce fluidity, retard its setting time, increase the porosity of the cement stone, and increase the number of pores with large sizes in the fly ash cement paste. The increase of porosity and pores with large sizes in cement decreases the compressive strength and increases the drying shrinkage of the fly ash cement paste.


Introduction
Coal produces large amounts of nitrogen oxides and CO 2 during combustion, resulting in a significant amount of environmental pollution [1,2]. Coal-fired power plants in China have completed the denitrification process, so the fly ash in China is denitrified fly ash containing ammonium salt. Ammonia slip is inevitable in the process of flue gas denitrification, and ammonium salt will be engendered and adsorbed on the fly ash particles due to the reaction of escaping NH 3 with the SO 3 of the flue gas. As a result, the problem of the utilization of denitrified fly ash is becoming more and more common in concrete. A large number of studies have shown that NH 4 HSO 4 is a by-product of denitrified fly ash [3][4][5][6][7][8][9].
Denitrified fly ash has many problems when used in building materials. Wu [10] found that the ready-mixed concrete with the denitrified fly ash caused uneven bubbles after the concrete was poured and bubble marks in concrete after the concrete hardened. Schert et al. [7] showed that the release rate of NH 3 gradually decreased to the level of undetectable in concrete with denitrified fly ash after three weeks of continuous release; however, a large amount of ammonia (20-70% relative to the initial level) remained in the concrete. He [11] showed that the ammonia of denitrified fly ash could influence the macroscopic properties of the fly ash cement paste, such as reduced rheological properties and decreased mechanical properties. Tan et al. [12] showed that denitrified fly ash can prolong the setting time and reduce the compressive and flexural strength of fly ash cement paste. Therefore, the application of denitrified fly ash in concrete will have many problems, such as prolonging the setting time [13], increasing the loss of fluidity [14], the appearance of a large number of bubbles and irritating odor on the surface of the concrete [15], leaving holes on the surface of the hardened concrete, causing the expansion of the concrete volume and decreasing the compressive strength [16], serious surface pulverization, etc. The problem of denitrified fly ash in the application of cementitious materials may be caused by the reaction between NH 4 + and OH − in the hydration process of cement to release ammonia and reduce the alkalinity of the cement paste. At present, there are few studies on the influence of NH 4 + on the properties of fly ash cement paste under the control of the anions (HSO 4 − ). The ammonia content in denitrified fly ash is also worthy of attention. According to the literature, the ratio of ammonia content adsorbed on fly ash (calculated from the mass fraction of NH 3 ) to ammonia concentration that escapes from the flue gas is around 50:1, and the ammonia content in denitrified fly ash ranges from 0-2500 ppm [7]. Zhang [17] collected and tested the nitrogen content of 30 fly ash samples from 15 power plants, and the results revealed that the ammonia content of most fly ash samples collected is less than 100 ppm. The ammonia content used in the study about denitrified fly ash was 0.1-6% [18,19], which differs greatly from the truly denitrified fly ash. In addition, the release of ammonia inevitably leads to changes in volume. However, there are few studies on the influence that ammonia content has on the volume of fly ash cement paste.
In this paper, the effect of Na + on cement hydration was widely investigated in the literature, so the effect of NH 4 + and Na + on the performance of fly ash cement paste was compared while the anions (HSO 4 − ) were held constant. In addition, the performance of cement paste was studied with the fly ash of different ammonia content, such as setting time, compressive strength, drying shrinkage, and pore structure. The ammonia content in fly ash was varied with the addition of NH 4 HSO 4 . These studies will provide a reference for the subsequent application of denitrified fly ash in cement.

Raw Materials
The fly ash used in the experiment was obtained from a power plant in Chongqing. The content of the fly ash was 30% in the fly ash blended cements. The initial ammonia content of the fly ash was 105 mg/kg, as determined by the fly ash rapid ammonia analyzer. The specific surface area of the fly ash was 434 m 2 /kg. The cement used in the experiment was 42.5R ordinary Portland cement produced by the Chongqing Xiaonanhai Cement Plant. The specific surface area of the cement was measured as 375 m 2 /kg by Brunauer-Emmett-Teller surface area measurement. The chemical composition of the fly ash and cement is listed in Table 1. Standard sand produced by Xiamen Aisiou Standard Sand Co., Ltd. (Xiamen, China) was used in the experiments. The density of the sand was 1.610 g/cm 3 , and the content of SiO 2 was 98.5%, which meets the GB/T17671-1999 "Method of testing cements -Determination of strength". The chemicals used in the experiment were analytically pure, mainly ammonium bisulfate (NH 4 HSO 4 ), sodium bisulfate (NaHSO 4 ), and ethanol. Tap water was used for the preparation the samples for the experiment, which is in accordance with the standard for water in concrete (JGJ63-2006). Deionized water was used for chemical analysis. The detailed mix proportions to compare the effects of NH 4 HSO 4 and NaHSO 4 are presented in Table 2. The mixed proportions of ammonia content are presented in Table 3.

Methods
The preparation and testing of the fluidity conformed to GB/T8077-2012. As the sample did not use additives, the water-binder ratio was 0.5. The setting time was determined using the Vicat apparatus following the Chinese standard procedure GB/T1346-2011, and the water-binder ratio was 0.4. The compressive strength was measured in accordance with the standard GB/T17671-1999, and the water-binder ratio was 0.4. The pressure testing machine was the TYE-300B produced by Wuxi Jianyi Instrument Machinery Co., Ltd. (Wuxi City, China).
According to the drying shrinkage test reference standard JC/T603-2004, the waterbinder ratio was 0.4. The fresh paste was cast into 25 mm × 25 mm × 280 mm metal cube molds and vibrated for 2 min to remove large air bubbles. After 24 h, the specimens were removed from the molds and the initial length L 0 measured. The specimens were cured in a room at a temperature of 20 ± 2 • C with a relative humidity of 65 ± 5% until testing. The length (L t ) of the specimen at different times was measured using a micrometer, and the drying shrinkage at different times was calculated using Equation (1): where S t is the drying shrinkage rate of the cement specimen at t days, L 0 is the initial length of the specimen, L t is the length of the specimen after t days, and 250 is the effective length of the specimen. The hydration heat of the fly ash cement paste was tested using a TAM Air 8 channel microcalorimeter produced by TA Instruments. The water-binder ratio was 0.4; the temperature of the water was adjusted to 20 • C; the duration of the test was 3 days.
The specimens cured to ages were broken apart, and the center of the specimens was collected in the form of small pieces. The hydration of the crushed solid was terminated by immersion in absolute ethyl alcohol and further vacuum drying at 40 • C to remove the solvent. Then, the samples were ground and sieved to 75 µm before the X-ray diffraction (XRD) and TG-DTG measurements. During the XRD test, the step length was set to 0.02 • , and the scanning time was 10 min. TG-DTG was used to analyze the change in mass of the cement hydration products during heating. The samples were heated from 30-1000 • C in a nitrogen atmosphere at a rate of 10 • C/min. The pore structure of the fly ash cement paste was tested using the mercury intrusion method; measurements were conducted using an AutoPore IV 9500 high-performance automatic mercury intrusion instrument produced by Micromeritics. Fly ash contains spherical particles with smooth surfaces and are smaller than the cement particles; thus, fly ash has both a morphological effect and micro-aggregate filling effect, which improve the workability, reduce water demand, and improve the fluidity of the mixture when used as mineral admixtures in cement and concrete [20]. However, the presence of the denitrification by-product NH 4 HSO 4 may instead reduce both the fluidity and fluidity loss of the fly ash cement paste when denitrified fly ash is used as a mineral admixture.

Results and Discussion
The effect of NH 4 HSO 4 and NaHSO 4 on the initial fluidity and fluidity after 1 h of the fly ash cement paste is shown in Figure 1. Fly ash without the addition of NH 4 HSO 4 and NaHSO 4 can improve the fluidity of the fly ash cement paste. However, the initial fluidity of the fly ash cement paste was reduced by 17.0% and 2.7%, when 2% NH 4 HSO 4 and 2% NaHSO 4 were added to the fly ash, respectively. This suggests that the influence of NH 4 HSO 4 on the fluidity of the fly ash cement paste is relatively large and implies that NH 4 + may affect the fluidity of the fly ash cement paste. Possible reasons for these observations are: (1) NH 4 + reacts with OHin water to generate NH 3 ·H 2 O after ammonium bisulfate is dissolved in water, which consumes the water in the paste and, thus, reduces its fluidity; (2) NH 4 + in ammonium bisulfate reacts with the Ca(OH) 2 generated during the early hydration of the cement to generate NH 3 ·H 2 O, which results in the release of ammonia. Ammonia will dissolve in water to produce NH 3 ·H 2 O and consume part of the water, decreasing the amount of water in the paste and, consequently, decreasing its fluidity. In summary, NH 4 + mainly affects the fluidity of the paste when denitrified fly ash is used in the cement paste. the cement hydration products during heating. The samples were heated from 30-1000 °C in a nitrogen atmosphere at a rate of 10 °C/min. The pore structure of the fly ash cement paste was tested using the mercury intrusion method; measurements were conducted using an AutoPore IV 9500 high-performance automatic mercury intrusion instrument produced by Micromeritics.

Fluidity
Fly ash contains spherical particles with smooth surfaces and are smaller than the cement particles; thus, fly ash has both a morphological effect and micro-aggregate filling effect, which improve the workability, reduce water demand, and improve the fluidity of the mixture when used as mineral admixtures in cement and concrete [20]. However, the presence of the denitrification by-product NH4HSO4 may instead reduce both the fluidity and fluidity loss of the fly ash cement paste when denitrified fly ash is used as a mineral admixture.
The effect of NH4HSO4 and NaHSO4 on the initial fluidity and fluidity after 1 h of the fly ash cement paste is shown in Figure 1. Fly ash without the addition of NH4HSO4 and NaHSO4 can improve the fluidity of the fly ash cement paste. However, the initial fluidity of the fly ash cement paste was reduced by 17.0% and 2.7%, when 2% NH4HSO4 and 2% NaHSO4 were added to the fly ash, respectively. This suggests that the influence of NH4HSO4 on the fluidity of the fly ash cement paste is relatively large and implies that NH4 + may affect the fluidity of the fly ash cement paste. Possible reasons for these observations are: (1) NH4 + reacts with OHin water to generate NH3·H2O after ammonium bisulfate is dissolved in water, which consumes the water in the paste and, thus, reduces its fluidity; (2) NH4 + in ammonium bisulfate reacts with the Ca(OH)2 generated during the early hydration of the cement to generate NH3·H2O, which results in the release of ammonia. Ammonia will dissolve in water to produce NH3·H2O and consume part of the water, decreasing the amount of water in the paste and, consequently, decreasing its fluidity. In summary, NH4 + mainly affects the fluidity of the paste when denitrified fly ash is used in the cement paste.

Setting Time
Fly ash can retard the setting time of the fly ash cement paste. The research on the influence of sulfate on cement hydration is as follows: gypsum (calcium sulfate) can adjust the setting time of cement paste; sodium sulfate is an early strength accelerator for cement

Setting Time
Fly ash can retard the setting time of the fly ash cement paste. The research on the influence of sulfate on cement hydration is as follows: gypsum (calcium sulfate) can adjust the setting time of cement paste; sodium sulfate is an early strength accelerator for cement that can promote early hydration. Alkali sulfates also have a significant influence on the setting time of cement. Hence, it is worth discussing the influence that NH 4 HSO 4 and NaHSO 4 have on the setting time of the fly ash cement paste.
Studies have shown that NH 4 HSO 4 in denitrified fly ash has a certain retarding effect [21,22]. This is possibly related to the higher concentration of sulfate ions introduced by NH 4 HSO 4 [19]. The influence of NH 4 HSO 4 and NaHSO 4 on the setting time of the fly ash cement paste is shown in Figure 2. Both NH 4 HSO 4 and NaHSO 4 retard the setting time, whereas the latter has a much smaller effect, which suggests that NH 4 + greatly slows down the hydration of the fly ash cement paste. that can promote early hydration. Alkali sulfates also have a significant influence on the setting time of cement. Hence, it is worth discussing the influence that NH4HSO4 and Na-HSO4 have on the setting time of the fly ash cement paste. Studies have shown that NH4HSO4 in denitrified fly ash has a certain retarding effect [21,22]. This is possibly related to the higher concentration of sulfate ions introduced by NH4HSO4 [19]. The influence of NH4HSO4 and NaHSO4 on the setting time of the fly ash cement paste is shown in Figure 2. Both NH4HSO4 and NaHSO4 retard the setting time, whereas the latter has a much smaller effect, which suggests that NH4 + greatly slows down the hydration of the fly ash cement paste.

Compressive Strength
When denitrified fly ash is used as a mineral admixture in cement and concrete engineering, different degrees of decline in compressive strength are observed. When NH4HSO4 in denitrified fly ash is used as a sulfate, it could excite the activity of the fly ash and improve the strength of the fly ash cement paste. However, the existence of NH4 + leads to the release of ammonia and affects the density of the cement stone, which may have a negative impact on the mechanical properties of the fly ash cement paste. Figure 3 shows the effect of NH4HSO4 and NaHSO4 on the compressive strength of the fly ash cement paste. The results showed that NH4HSO4 can reduce the compressive strength of the fly ash cement paste, and the compressive strength of 1 d was 22.8% lower than that of the fly ash cement paste without NH4HSO4. The compressive strength of the fly ash cement paste with NaHSO4 was 1.3% and 14.3% higher than the samples without NaHSO4 after 1 and 3 days, respectively, while the compressive strengths of the samples after 7 and 28 days were effectively identical. This suggests that NH4 + reduces the compressive strength of the fly ash cement paste.

Drying Shrinkage
The mixing of fly ash into cement paste will reduce its drying shrinkage [20]. However, NH4 + ions contained within NH4HSO4 present in denitrified fly ash may react with OHin both the water and calcium hydroxide generated by cement hydration to release ammonia, which can influence the drying shrinkage of the fly ash cement paste.

Compressive Strength
When denitrified fly ash is used as a mineral admixture in cement and concrete engineering, different degrees of decline in compressive strength are observed. When NH 4 HSO 4 in denitrified fly ash is used as a sulfate, it could excite the activity of the fly ash and improve the strength of the fly ash cement paste. However, the existence of NH 4 + leads to the release of ammonia and affects the density of the cement stone, which may have a negative impact on the mechanical properties of the fly ash cement paste. Figure 3 shows the effect of NH 4 HSO 4 and NaHSO 4 on the compressive strength of the fly ash cement paste. The results showed that NH 4 HSO 4 can reduce the compressive strength of the fly ash cement paste, and the compressive strength of 1 d was 22.8% lower than that of the fly ash cement paste without NH 4 HSO 4 . The compressive strength of the fly ash cement paste with NaHSO 4 was 1.3% and 14.3% higher than the samples without NaHSO 4 after 1 and 3 days, respectively, while the compressive strengths of the samples after 7 and 28 days were effectively identical. This suggests that NH 4 + reduces the compressive strength of the fly ash cement paste. The effects of NH4HSO4 and NaHSO4 on the drying shrinkage of the fly ash cement paste are shown in Figure 4. Without the addition of sulfate, fly ash can reduce the drying shrinkage of the fly ash cement paste, while the addition of NH4HSO4 and NaHSO4 results in a clear increase in the drying shrinkage of the fly ash cement paste. In addition, the drying shrinkage of the fly ash cement paste containing NH4HSO4 was larger than that of The mixing of fly ash into cement paste will reduce its drying shrinkage [20]. However, NH 4 + ions contained within NH 4 HSO 4 present in denitrified fly ash may react with OHin both the water and calcium hydroxide generated by cement hydration to release ammonia, which can influence the drying shrinkage of the fly ash cement paste.
The effects of NH 4 HSO 4 and NaHSO 4 on the drying shrinkage of the fly ash cement paste are shown in Figure 4. Without the addition of sulfate, fly ash can reduce the drying shrinkage of the fly ash cement paste, while the addition of NH 4 HSO 4 and NaHSO 4 results in a clear increase in the drying shrinkage of the fly ash cement paste. In addition, the drying shrinkage of the fly ash cement paste containing NH 4 HSO 4 was larger than that of the samples that contained NaHSO 4 , indicating that NH 4 + has a greater influence on the drying shrinkage. One possibility is that NH 4 HSO 4 in denitrified fly ash reacts with water, and the volatilization of NH 3 ·H 2 O also removes the water, increasing the drying shrinkage. The volatilization of NH 3 itself also can cause the contraction of the paste. Another possibility is that the release of ammonia causes the opening porosity of the hardened fly ash cement paste to increase, which accelerates the loss of water and leads to drying shrinkage. Therefore, NH 4 + in denitrified fly ash will increase the drying shrinkage of the fly ash cement paste. The effects of NH4HSO4 and NaHSO4 on the drying shrinkage of the fly ash cement paste are shown in Figure 4. Without the addition of sulfate, fly ash can reduce the drying shrinkage of the fly ash cement paste, while the addition of NH4HSO4 and NaHSO4 results in a clear increase in the drying shrinkage of the fly ash cement paste. In addition, the drying shrinkage of the fly ash cement paste containing NH4HSO4 was larger than that of the samples that contained NaHSO4, indicating that NH4 + has a greater influence on the drying shrinkage. One possibility is that NH4HSO4 in denitrified fly ash reacts with water, and the volatilization of NH3·H2O also removes the water, increasing the drying shrinkage. The volatilization of NH3 itself also can cause the contraction of the paste. Another possibility is that the release of ammonia causes the opening porosity of the hardened fly ash cement paste to increase, which accelerates the loss of water and leads to drying shrinkage. Therefore, NH4 + in denitrified fly ash will increase the drying shrinkage of the fly ash cement paste.

Heat of Hydration
The addition of fly ash reduces the exothermic peak of cement hydration and delays the time at which this peak occurs. As a sulfate, NH 4 HSO 4 may also affect the hydration heat of the fly ash cement paste. Therefore, the effects of NH 4 HSO 4 and NaHSO 4 on the hydration heat of the fly ash cement paste were studied.
The effect of NH 4 HSO 4 and NaHSO 4 on the heat of hydration of the fly ash cement paste is shown in Figure 5. The hydration heat peak of the fly ash cement paste containing NH 4 HSO 4 and NaHSO 4 was observed to be lower than that of the samples without sulfate, and the peak of the hydration heat was delayed; notably, the peak hydration heat reached by samples containing NaHSO 4 was higher than that of those that contained NH 4 HSO 4 . This indicates that both NH 4 HSO 4 and NaHSO 4 slow down the process of cement hydration, but NH 4 HSO 4 results in longer delays. In terms of the total amount of heat released, the heat of hydration released by the fly ash cement paste containing NH 4 HSO 4 and NaHSO 4 was slightly lower than samples without sulfate in the first 30 h; however, the total heat release was greater after this time had elapsed. This suggests that NH 4 HSO 4 and NaHSO 4 reduce the total hydration heat of the fly ash cement paste in the first 30 h of hydration.
After 30 h, the sulfates may stimulate the activity of the fly ash, promoting the secondary hydration of the fly ash and increasing the total hydration heat of the fly ash cement paste.
This indicates that both NH4HSO4 and NaHSO4 slow down the process of cement hydration, but NH4HSO4 results in longer delays. In terms of the total amount of heat released, the heat of hydration released by the fly ash cement paste containing NH4HSO4 and Na-HSO4 was slightly lower than samples without sulfate in the first 30 h; however, the total heat release was greater after this time had elapsed. This suggests that NH4HSO4 and Na-HSO4 reduce the total hydration heat of the fly ash cement paste in the first 30 h of hydration. After 30 h, the sulfates may stimulate the activity of the fly ash, promoting the secondary hydration of the fly ash and increasing the total hydration heat of the fly ash cement paste.

Hydration Products
C-S-H, Ca(OH)2, and other hydration products are generated when cement reacts with water. The types of cement hydration products are closely related to their mechanical properties and volume stability. The addition of NH4HSO4 and NaHSO4 may affect the hydration products of the fly ash cement paste. The effects of NH4HSO4 and NaHSO4 on the hydration products of the fly ash cement paste at different ages were studied by XRD and TG.
The XRD patterns of the hydration products of the fly ash cement paste with NH4HSO4 and NaHSO4 after 1 day and after 28 days is shown in Figure 6. NH4HSO4 and NaHSO4 do not affect the types of hydration products of the fly ash cement paste at different ages, i.e., no new hydration products were generated, indicating that NH4HSO4 and NaHSO4 do not affect the hydration products generated in the fly ash cement paste. In addition, a semi-quantitative analysis of the hydration products was carried out according to the diffraction peaks. After one day, the diffraction peaks associated with calcium hydroxide in the samples containing NH4HSO4 and NaHSO4 were relatively low, which may be due to the consumption of calcium hydroxide by NH4 + and H + . There was no significant

Hydration Products
C-S-H, Ca(OH) 2 , and other hydration products are generated when cement reacts with water. The types of cement hydration products are closely related to their mechanical properties and volume stability. The addition of NH 4 HSO 4 and NaHSO 4 may affect the hydration products of the fly ash cement paste. The effects of NH 4 HSO 4 and NaHSO 4 on the hydration products of the fly ash cement paste at different ages were studied by XRD and TG.
The XRD patterns of the hydration products of the fly ash cement paste with NH 4 HSO 4 and NaHSO 4 after 1 day and after 28 days is shown in Figure 6. NH 4 HSO 4 and NaHSO 4 do not affect the types of hydration products of the fly ash cement paste at different ages, i.e., no new hydration products were generated, indicating that NH 4 HSO 4 and NaHSO 4 do not affect the hydration products generated in the fly ash cement paste. In addition, a semi-quantitative analysis of the hydration products was carried out according to the diffraction peaks. After one day, the diffraction peaks associated with calcium hydroxide in the samples containing NH 4 HSO 4 and NaHSO 4 were relatively low, which may be due to the consumption of calcium hydroxide by NH 4 + and H + . There was no significant difference in the amount of calcium hydroxide in the samples after 28 days, indicating that the NH 4 HSO 4 and NaHSO 4 mainly affect the concentration of calcium hydroxide in the early stages of hydration.
The TGA spectra that describes the influence of NH 4 HSO 4 and NaHSO 4 on the hydration products of the fly ash cement paste after 1 d and 28 d is shown in Figure 7. The decomposition peak of ettringite and C-S-H gel was at 70-100 • C, while the decomposition peak of calcium hydroxide occurred between 420 and 475 • C [23]. The calcium hydroxide production in the cement paste samples that contained NH 4 HSO 4 and NaHSO 4 was observed to be lower than that in samples without sulfate after one day, which is consistent with the XRD test results, supporting the theory that NH 4 + and H + consume a portion of the available calcium hydroxide. Furthermore, at 1 day, the reactivity of the cement was delayed in the presence of NH 4 HSO 4 , so less portlandite was produced. After 28 days, there was no difference in the amount of calcium hydroxide present in the samples containing NH 4 HSO 4 and the samples containing NaHSO 4 . difference in the amount of calcium hydroxide in the samples after 28 days, indicating that the NH4HSO4 and NaHSO4 mainly affect the concentration of calcium hydroxide in the early stages of hydration. The TGA spectra that describes the influence of NH4HSO4 and NaHSO4 on the hydration products of the fly ash cement paste after 1 d and 28 d is shown in Figure 7. The decomposition peak of ettringite and C-S-H gel was at 70-100 °C, while the decomposition peak of calcium hydroxide occurred between 420 and 475 °C [23]. The calcium hydroxide production in the cement paste samples that contained NH4HSO4 and NaHSO4 was observed to be lower than that in samples without sulfate after one day, which is consistent with the XRD test results, supporting the theory that NH4 + and H + consume a portion of the available calcium hydroxide. Furthermore, at 1 day, the reactivity of the cement was delayed in the presence of NH4HSO4, so less portlandite was produced. After 28 days, there was no difference in the amount of calcium hydroxide present in the samples containing NH4HSO4 and the samples containing NaHSO4.  The results obtained in Section 3.1 indicate that the NH 4 + in NH 4 HSO 4 reduces the fluidity of the fly ash cement paste, retards its setting time, decreases its compressive strength, and increases its drying shrinkage, but does not affect the hydration products produced. However, the ammonia content of 2% NH 4 HSO 4 and actual denitrified fly ash (0-2500 ppm) is quite different [16], and there have been few studies on the effects of ammonia content on the volume and pore structure of fly ash cement paste. Thus, the study of the effects of ammonia content on the volume change of cement-based materials is of practical significance.

Fluidity
The results presented in Section 3.1.1 showed that NH 4 + reduces the initial fluidity of the fly ash cement paste and increases the fluidity loss. The change in the fluidity of the fly ash cement paste in the samples with varying ammonia contents is shown in Figure 8. It can be seen that the fluidity of the fly ash cement paste increases with the increase of ammonia content. When no ammonia was added to the fly ash, the initial fluidity of the fly ash cement paste was 5.3% higher than that of the cement paste. However, as the additional ammonia content increased, the fluidity of the fly ash cement paste decreased significantly. When the additional ammonia content was 200 mg/kg, the initial fluidity of the fly ash cement paste was still 2% greater than that of cement paste. However, when the additional ammonia content in the fly ash was 400 mg/kg, the initial fluidity of the fly ash cement paste was equivalent to that of the cement paste. Finally, when the additional ammonia content of the denitrified fly ash exceeded 400 mg/kg, the fluidity of cement paste was reduced rather than increased.

Setting time
The results presented in Section 3.1.2 showed that denitrified fly ash retarded the setting time of the fly ash cement paste. The effect of increasing ammonium content on the setting time of the fly ash cement paste is shown in Figure 9. It was observed that when the additional ammonia content was less than 1000 mg/kg, there was no obvious trend that governed the initial setting time of the samples as the ammonia content increased. When more than 1000 mg/kg of ammonia was added, the initial setting time of the fly ash cement paste was increased as the amount of additional ammonia increased. In addition, when the additional ammonia content was greater than 400 mg/kg, the final setting time of the fly ash cement paste was increasingly prolonged with the additional ammonia content of the fly ash. Overall, increasing the ammonia content of the denitrified fly ash would prolong the cement paste's initial and final setting times. This was related to the consumption of OH − by NH4 + and H + from NH4HSO4, which decreased the alkalinity of the paste.  In addition, the fluidity loss of the samples after the first hour decreased and then increased. When the additional ammonia content was less than 1000 mg/kg, the fluidity loss after the first hour exhibited a decreasing trend. Notably, the fluidity loss after the first hour of the fly ash cement paste when 1000 mg/kg ammonia was added was 52.5% lower than that of the sample without any added ammonia. One possibility was that the release of ammonia led to the emergence of small bubbles in the fly ash cement paste, which potentially lubricated the paste. When the additional ammonia content exceeded 1000 mg/kg, the fluidity loss increased over time; specifically, the one-hour fluidity loss in the sample with 5000 mg/kg of additional ammonia was 79% greater than in the sample where only 1000 mg/kg ammonia was added. This could be because ammonia was very soluble in water when the paste was saturated with ammonia, and it will form NH 3 ·H 2 O with the water in the paste. In addition, the volatilization of NH 3 ·H 2 O will also consume some of the water in the system. This negative effect of the loss of water on the fluidity of the fly ash cement paste is greater than the increase in fluidity provided by the bubbles generated by this process, resulting in the overall fluidity loss of the fly ash cement paste over time.

Setting time
The results presented in Section 3.1.2 showed that denitrified fly ash retarded the setting time of the fly ash cement paste. The effect of increasing ammonium content on the setting time of the fly ash cement paste is shown in Figure 9. It was observed that when the additional ammonia content was less than 1000 mg/kg, there was no obvious trend that governed the initial setting time of the samples as the ammonia content increased. When more than 1000 mg/kg of ammonia was added, the initial setting time of the fly ash cement paste was increased as the amount of additional ammonia increased. In addition, when the additional ammonia content was greater than 400 mg/kg, the final setting time of the fly ash cement paste was increasingly prolonged with the additional ammonia content of the fly ash. Overall, increasing the ammonia content of the denitrified fly ash would prolong the cement paste's initial and final setting times. This was related to the consumption of OH − by NH 4 + and H + from NH 4 HSO 4 , which decreased the alkalinity of the paste.

Setting time
The results presented in Section 3.1.2 showed that denitrified fly ash retarded the setting time of the fly ash cement paste. The effect of increasing ammonium content on the setting time of the fly ash cement paste is shown in Figure 9. It was observed that when the additional ammonia content was less than 1000 mg/kg, there was no obvious trend that governed the initial setting time of the samples as the ammonia content increased. When more than 1000 mg/kg of ammonia was added, the initial setting time of the fly ash cement paste was increased as the amount of additional ammonia increased. In addition, when the additional ammonia content was greater than 400 mg/kg, the final setting time of the fly ash cement paste was increasingly prolonged with the additional ammonia content of the fly ash. Overall, increasing the ammonia content of the denitrified fly ash would prolong the cement paste's initial and final setting times. This was related to the consumption of OH − by NH4 + and H + from NH4HSO4, which decreased the alkalinity of the paste.

Compressive Strength
The results presented in Section 3.1.3 showed that NH 4 HSO 4 reduced the compressive strength of the fly ash cement paste. The effect of increasing ammonia content in denitrified fly ash on the compressive strength of the fly ash cement paste is shown in Figure 10. It could be seen that the compressive strength of the fly ash cement paste after 1, 3, 7, and 28 days exhibited a downward trend as the ammonia content of the denitrified fly ash increased. When the additional ammonia content of the fly ash was more than 1000 mg/kg, the compressive strength decreased significantly. When the additional ammonia content was 5000 mg/kg, the compressive strength of fly ash cement paste after three days was 28.75% lower than the same value recorded when only 1000 mg/kg of additional ammonia was added. This suggests that the compressive strength of the fly ash cement paste decreased as the ammonia content of the denitrified fly ash increased. and 28 days exhibited a downward trend as the ammonia content of the denitrified fly ash increased. When the additional ammonia content of the fly ash was more than 1000 mg/kg, the compressive strength decreased significantly. When the additional ammonia content was 5000 mg/kg, the compressive strength of fly ash cement paste after three days was 28.75% lower than the same value recorded when only 1000 mg/kg of additional ammonia was added. This suggests that the compressive strength of the fly ash cement paste decreased as the ammonia content of the denitrified fly ash increased.

Drying Shrinkage
According to Section 3.1.4, NH4HSO4 increases the drying shrinkage of the fly ash cement paste. The drying shrinkage of the fly ash cement paste with low ammonia content is unknown. The effect of increasing ammonia content on the drying shrinkage of the fly ash cement paste is shown in Figure 11. Compared to pure cement paste, the fly ash with no additional ammonia content can reduce the drying shrinkage experienced by the fly ash cement paste in the early stages. As the ammonia content of denitrified fly ash increased, the drying shrinkage of the cement paste also increased. When the amount of ammonia added was less than or equal to 800 mg/kg, the fly ash still reduced the drying shrinkage of the cement paste compared to pure cement paste. However, when more than 800 mg/kg of ammonia was added, the dry shrinkage of the fly ash cement paste was increased compared to pure cement paste; above these values, the dry shrinkage of the fly ash cement paste increased as the ammonia content increased. In addition, after 56 days, the drying shrinkage of samples with an additional ammonia content of 5000 mg/kg was 62.4% greater compared to the fly ash cement paste without any additional ammonia and 5.8% greater compared to pure cement paste. These observations could be explained by the fact that during the reaction of NH4HSO4 with cement and water, the release of ammonia removed a portion of the available water while also increasing the opening porosity

Drying Shrinkage
According to Section 3.1.4, NH 4 HSO 4 increases the drying shrinkage of the fly ash cement paste. The drying shrinkage of the fly ash cement paste with low ammonia content is unknown. The effect of increasing ammonia content on the drying shrinkage of the fly ash cement paste is shown in Figure 11. Compared to pure cement paste, the fly ash with no additional ammonia content can reduce the drying shrinkage experienced by the fly ash cement paste in the early stages. As the ammonia content of denitrified fly ash increased, the drying shrinkage of the cement paste also increased. When the amount of ammonia added was less than or equal to 800 mg/kg, the fly ash still reduced the drying shrinkage of the cement paste compared to pure cement paste. However, when more than 800 mg/kg of ammonia was added, the dry shrinkage of the fly ash cement paste was increased compared to pure cement paste; above these values, the dry shrinkage of the fly ash cement paste increased as the ammonia content increased. In addition, after 56 days, the drying shrinkage of samples with an additional ammonia content of 5000 mg/kg was 62.4% greater compared to the fly ash cement paste without any additional ammonia and 5.8% greater compared to pure cement paste. These observations could be explained by the fact that during the reaction of NH 4 HSO 4 with cement and water, the release of ammonia removed a portion of the available water while also increasing the opening porosity of the hardened fly ash cement paste; this increased the contact area between the specimen and the external environment, which accelerated the loss of water and increased drying shrinkage. Furthermore, the volume expansion experienced by the one-day-old fly ash cement paste with an additional ammonia content of 5000 mg/kg could be explained by the high ammonia content, which accelerated the early release of ammonia and resulted in volume expansion.
of the hardened fly ash cement paste; this increased the contact area between the specimen and the external environment, which accelerated the loss of water and increased drying shrinkage. Furthermore, the volume expansion experienced by the one-day-old fly ash cement paste with an additional ammonia content of 5000 mg/kg could be explained by the high ammonia content, which accelerated the early release of ammonia and resulted in volume expansion.  Figure 11. The effect of increasing fly ash ammonia content on the drying shrinkage of cement paste.

Pore Structure
Previous studies have suggested that the pore structure of cement concrete can be improved and that the volume of large pores in the paste decreases when fly ash is added into cement concrete as the mineral admixture; this is beneficial to the late strength of the fly ash cement paste [20,24]. The results described in Sections 3.1.4 and 3.2.4 indicate that the NH4HSO4 in denitrified fly ash led to the release of ammonia, increased the drying shrinkage of the fly ash cement paste, and led to volume expansion, which may affect the internal structure of the cement after hardening, as well as affect the pore structure of the fly ash cement paste. Thus, mercury injection was used to study the effect of increasing ammonia content in denitrified fly ash on the pore structure of the resultant cement paste.
The changes in the porosity and pore size distribution of the fly ash cement paste with increasing ammonia content is shown in Figure 12. As the ammonia content increased, the number of large pores in the cement paste increased while the number of small pores decreased. This was especially significant in the number of pores with sizes greater than 200 nm; the number of pores larger than 200 nm after 7 and 28 days in samples with 1000 mg/kg of additional ammonia content increased by 5.9% and 0.6%, respectively, compared to samples without any additional ammonia. Considering that NH4HSO4 in denitrified fly ash led to the release of ammonia gas, as the ammonia content increased, the porosity and the number of large pores in the fly ash cement paste also increased, which adversely affected the strength and volume shrinkage of the cement paste. The results of the pore structure experiments were consistent with the previous results obtained regarding the compressive strength and drying shrinkage of the cement pastes.

Pore Structure
Previous studies have suggested that the pore structure of cement concrete can be improved and that the volume of large pores in the paste decreases when fly ash is added into cement concrete as the mineral admixture; this is beneficial to the late strength of the fly ash cement paste [20,24]. The results described in Sections 3.1.4 and 3.2.4 indicate that the NH 4 HSO 4 in denitrified fly ash led to the release of ammonia, increased the drying shrinkage of the fly ash cement paste, and led to volume expansion, which may affect the internal structure of the cement after hardening, as well as affect the pore structure of the fly ash cement paste. Thus, mercury injection was used to study the effect of increasing ammonia content in denitrified fly ash on the pore structure of the resultant cement paste.
The changes in the porosity and pore size distribution of the fly ash cement paste with increasing ammonia content is shown in Figure 12. As the ammonia content increased, the number of large pores in the cement paste increased while the number of small pores decreased. This was especially significant in the number of pores with sizes greater than 200 nm; the number of pores larger than 200 nm after 7 and 28 days in samples with 1000 mg/kg of additional ammonia content increased by 5.9% and 0.6%, respectively, compared to samples without any additional ammonia. Considering that NH 4 HSO 4 in denitrified fly ash led to the release of ammonia gas, as the ammonia content increased, the porosity and the number of large pores in the fly ash cement paste also increased, which adversely affected the strength and volume shrinkage of the cement paste. The results of the pore structure experiments were consistent with the previous results obtained regarding the compressive strength and drying shrinkage of the cement pastes.

Conclusions
(1) Compared with cement slurry without NH4HSO4, when the NH4HSO4 content was 2%, the fluidity of the paste decreased by 17.0%, the initial setting time lengthened

Conclusions
(1) Compared with cement slurry without NH 4 HSO 4 , when the NH 4 HSO 4 content was 2%, the fluidity of the paste decreased by 17.0%, the initial setting time lengthened by 12.8%, and the compressive strength of 1 d decreased by 22.8%. When the NaHSO 4 content was 2%, the fluidity of the paste decreased by 2.7% and initial setting time lengthened by 8.5%. The 1 d's compressive strength increased by 1.3%, and it was found that the NH 4+ in the by-product of denitrified fly ash was the main reason that affected the performance of the fly ash cement paste, while NH 4+ obviously reduced the fluidity of the fly ash cement paste and retarded the setting time of the fly ash cement paste. (2) Through hydration heat and TG analysis, NH 4+ will reduce the peak and total heat release of the fly ash cement paste during hydration and affect the calcium hydroxide hydrate content. (3) When the content of NH 4 HSO 4 was 1000 mg/kg, the number of large pores in the net paste of the fly ash cement increased by 5.9% and 0.6% at 7d and 28d, respectively, compared with that of the net paste of the fly ash cement with the content of NH 4 HSO 4 being 0 mg/kg. Therefore, NH 4+ will increase the porosity of the cement stone and the number of macropores in the fly ash cement paste, thereby reducing the strength of the fly ash cement paste and increasing the drying shrinkage of the fly ash cement paste. In practical engineering, ammonia content in denitrified fly ash should be strictly controlled. Institutional Review Board Statement: Not applicable.

Informed Consent Statement: Not applicable.
Data Availability Statement: Not applicable.

Conflicts of Interest:
The authors declare that they have no known competing financial interest or personal relationships that could have appeared to influence the work reported in this paper.