- 1College of Water Resources and Architecture Engineering, Tarim University, Xinjiang, China
- 2Key Laboratory of Tarim Oasis Agriculture (Tarim University), Ministry of Education, Alaer, China
Flue gas desulfurization gypsum (FGD) and biochar are considered effective amendments for alleviating soil salinity stress. However, the co-application of these amendments in practice requires further investigation. This study successfully prepared a superabsorbent carbon-based material (CB) via graft polymerization and applied it in combination with FGD to investigate their effects on leaching salt ions and improving saline-alkali soil. A laboratory soil column leaching experiment was conducted with six treatments: control (CK, no amendment), cotton straw biochar (BC), CB, FGD, BC+FGD, and CB+FGD. Field plot trials were further employed to evaluate the soil amendment efficacy. The results demonstrated that the co-application of the CB and FGD significantly alleviated salt stress by promoting Na+ leaching. During the P1 (sharp decrease) leaching phase, Na+ leaching concentrations under the sole FGD and CB+FGD treatments increased by 89.08% and 90.92%, respectively, compared to CK. Co-application with FGD significantly increased the content of Ca2+ and SO42- in the soil. The CB effectively retained soil K+, and the Cl- content after leaching was significantly lower than in CK. Field trials further confirmed that the co-application of the CB and FGD significantly reduced the contents of Na+, Cl-, and Mg2+ while increasing the contents of Ca2+, K+, and SO42-. The contents of Na+, Cl-, and K+ increased with soil depth, indicating the migration of major salt ions towards deeper soil layers with water movement. The CB+FGD treatment significantly reduced soil TSS, electrical conductivity (EC), and SAR. In conclusion, the co-application between the CB and FGD enhances salt leaching efficiency and soil water retention capacity, exerting a positive influence on the remediation of saline-alkali soils. This study provides a novel strategy for utilizing agricultural waste in saline soil management.
1 Introduction
Soil salinization has become a major factor in global soil degradation (1). Globally, salinized land covers approximately 1.7 × 109 hectares (2), with nearly 100 million hectares located in China, primarily distributed across arid and semi-arid regions (3). Soil salinization leads to poor soil nutrient availability and low utilization efficiency, thereby adversely affecting crop yields and posing a significant constraint to global agricultural production (4). Nevertheless, saline-alkali soils possess substantial potential for development and utilization, making their amelioration crucial for achieving sustainable agriculture. Traditional reclamation techniques, such as leaching and salt drainage, cultivating salt-tolerant crops, and applying soil amendments, suffer from limitations including high water dependency, susceptibility to amendment loss, and concurrent depletion of soil nutrients (3).
Biochar is a carbon-rich material produced through the pyrolysis of organic waste (3). It is recognized as an effective amendment for alleviating salt stress in soils and has been widely applied to improve soil properties (1, 5–7). Studies indicate that biochar can enhance soil nutrients, promote crop growth, and increase crop yield (8–10). However, the influence of biochar on soil water retention and salt suppression characteristics primarily depends on the feedstock (10), pyrolysis conditions (11), particle size (12, 13), application rate (10, 14), and soil type (13). Furthermore, its effectiveness is constrained by its internal pore structure, specific surface area, and the content of hydrophobic functional groups (10–14), resulting in inherently limited water retention and salt suppression potential. Its application in saline soils may even exacerbate the loss of soil moisture and nutrients. Therefore, our research team previously synthesized three types of superabsorbent carbon-based materials using biochar combined with chitosan and sodium alginate. These materials demonstrated excellent water absorption properties (15).
Superabsorbent carbon-based materials are a novel class of biochar-based soil amendments prepared through physical or chemical methods. Characterized by high water absorption capacity and unique pore structures, they are cross-linked hydrophilic polymers exhibiting superior water absorption and retention potential (14). Their key features include high water absorption and retention capacity (16), large specific surface area (3), abundant functional groups (e.g., hydroxyl, carboxyl) (17), as well as good biocompatibility and environmental friendliness. In soil remediation, these materials can absorb and retain water, thereby improving soil moisture status and aggregate structure, enhancing soil aeration and nutrient retention capacity, creating a favorable micro-environment for crop growth (18, 19), and promoting root development (7, 17).
Due to their rich functional groups and porous structure, superabsorbent carbon-based materials can adsorb soil salt ions (e.g., Na+, Cl-) or reduce soil salinity by enhancing pore water flow, mitigating salt stress on plants (14, 20). Gypsum, composed of fine particles with low water content, can reduce salinity and alkalinity in saline-alkali soils and improve soil structure and permeability (1). Additionally, gypsum supplies essential mineral nutrients like Ca, S, and Si, aiding plant growth and enhancing seedling emergence rates and yields in saline lands (21). Co-application of flue gas desulfurization gypsum (FGD) in saline-alkali soils can regulate soil pH, replenish mineral elements, decrease salinity, and improve fertility, thereby helping to mitigate soil salinization/alkalization and promoting crop growth (22, 23).
However, research on the mechanisms by which carbon-based materials and FGD suppress salinity and retain water in saline-alkali soils is scarce. The efficacy varies considerably among different types of carbon-based materials (1, 10, 24), and the key factors governing their interaction with saline soils—such as application rate, particle size, and types of functional groups—remain unclear.
Given that superabsorbent carbon-based materials and FGD individually reduce salinity (1, 25), alleviate salt stress (26, 27), and enhance soil water retention (17, 19), we hypothesize that their co-application will synergistically improve salt leaching efficiency and soil water retention capacity in saline soils, surpassing the effects of individual applications. The primary objectives of this study are as follows: (1) To investigate the dynamic effects of applying the superabsorbent carbon-based material alone and in combination with FGD on salinity in saline soil; (2) To determine the optimal treatment involving the co-application of the superabsorbent carbon-based material and FGD; (3) To establish the causal relationships between soil salt ions and key soil physicochemical properties following the application of the superabsorbent carbon-based material alone and in combination with FGD.
2 Materials and methods
2.1 Study area description
The experimental site is located at Tarim University (40°32’32”N, 81°17’11”E), Xinjiang Uygur Autonomous Region, situated in the hinterland of the Tarim Basin. The region experiences a typical warm-temperate continental climate characterized by extreme aridity, abundant sunshine, significant diurnal temperature variations, low precipitation, and high evaporation. The basin receives <100 mm average annual precipitation, while potential evaporation ranges from 1800–2900 mm (28). Mean annual temperature varies between 10.6–11.5°C, with recorded extremes of 43.6°C and -30.9°C (29). The predominant soils in the area are saline-alkali soils with an exchangeable sodium percentage (ESP) of 34.42%. Cotton is the main cultivated crop in this area.
2.2 Materials
The test soil was collected from saline-alkali soil within the experimental area. Soil samples were taken from the 0–20 cm depth profile, air-dried under natural conditions, sieved to remove impurities, and passed through a 2-mm sieve. The soil texture was classified as sandy loam (sand: 75.58%, silt: 24.03%, clay: 0.39%). The superabsorbent carbon-based material used in the experiments was synthesized through the following process: cotton straw was pyrolyzed under oxygen-limited conditions at 600°C to produce biochar (BC), which was subsequently crushed, sieved, and modified with chitosan to yield the chitosan-modified superabsorbent carbon-based material (CB) (15), facilitating the resource reuse of waste cotton stalks. Key material characterization data are provided in Supplementary Figures S1-S3. FGD was obtained from Alar Shengyuan Thermal Power Co., Ltd. The FGD material presented as an off-white powder (particle size: 30–60 µm) with calcium sulfate dihydrate (CaSO4·2H2O) comprising >90% of its mass. The basic physicochemical properties of the test soil are presented in Table 1.
2.3 Experimental design
2.3.1 Salt leaching experiment
A one-dimensional vertical infiltration method with constant water head was employed to investigate the effects of carbon-based materials and their co-application with flue FGD on soil salt leaching. The experiment utilized plexiglass soil columns (inner diameter: 10 cm, height: 35 cm) connected to a Mariotte bottle water supply system (Figure 1). Six treatments were established: CK (control, no amendment), BC (cotton straw biochar alone), CB (chitosan-modified superabsorbent carbon-based material alone), FGD (flue gas desulfurization gypsum alone), BC+FGD, and CB+FGD. Amendments were uniformly mixed into the 0–20 cm soil layer at an application rate of 0.5% (w/w). Each soil column was filled to a height of 30 cm. For co-application treatments (BC+FGD and CB+FGD), FGD was added simultaneously. Each treatment was replicated three times. The initial breakthrough time of leachate was recorded following the methodology described by Yue et al. (30). Changes in the electrical conductivity (EC) of the leachate were dynamically monitored. Based on the characteristics of the EC decline, the leaching process was divided into three distinct phases: a rapid decline phase (P1, EC ≈ 60% of initial value), a gradual decline phase (P2, EC ≈ 90% of initial value), and a stable phase (P3). The experiment was terminated when the EC of the leachate decreased to 5 mS·cm-¹ (corresponding to a total salt content of approximately 3 g·L-¹) and stabilized.
2.3.2 Field experiment
Field experiments were conducted from April to November 2023 at the Water-saving Irrigation Experimental Station of Tarim University. PVC cylinders (top diameter: 29 cm, bottom diameter: 26 cm, height: 36 cm) were used. Nine evenly spaced aeration holes (diameter = 5 mm) were drilled in the bottom. Each cylinder was filled with soil to a depth of 30 cm. Amendments (superabsorbent CB and/or FGD) were incorporated into the top 0–20 cm soil layer. Six treatments were established (identical to those described in Section 2.3.1 for the column leaching experiment). Cotton (Gossypium hirsutum L. cv. ‘Tahe No. 2’) was planted, with two seedlings per cylinder. During the entire cotton growth period, irrigation was applied 12 times (total irrigation amount: 3000 m3·ha-2; single application: 250 m3·ha-2; interval: 6–7 days). Compound fertilizer (15-15–15 N-P2O5-K2O) was applied as basal dressing at 5.4 g per column. Conventional topdressing (urea + compound fertilizer) was subsequently applied with irrigation at rates of 375 kg N ha-¹, 450 kg P2O5 ha-¹, and 150 kg K2O ha-¹. Fertilization and all other cultivation and management practices were consistent across all treatments and aligned with local field practices. Each treatment was replicated three times.
2.4 Measurements and methods
Salt ion concentrations (K+, Na+, Ca2+, Mg2+, HCO3-, SO42-, and Cl-) were determined in the leachate collected during each leaching phase and in the soil layers after leaching. For the field experiment, soil salt ion concentrations at depths of 0–20 cm and 20–30 cm within the cylinders were measured at seeding stage, bud stage, flowering and boll stage, boll-opening stage. Soil EC was measured at the boll-opening stage. K+ and Na+ were determined by flame photometry (AP-1200, Shanghai Precision Instrument Co., China). Ca2+ and Mg2+ were determined by EDTA complexometric titration (10). HCO3- was determined by acid-base titration (31). SO42- was determined by indirect EDTA titration (32). Cl- was determined by silver nitrate titration (31). Total soluble salts (TSS) were calculated as the sum of the concentrations of water-soluble anions and cations. The sodium adsorption ratio (SAR) was calculated using Equation 1 (33):
Where [Na+], [Ca2+] and [Mg2+] are the concentrations (mmol·L−1) of sodium, calcium, and magnesium ions in the soil solution.
2.5 Data processing and analysis
Experimental data are expressed as the mean ± standard deviation (SD) of three replicates. Statistical analyses were performed using SPSS 26.0 software. One-way analysis of variance (ANOVA) was employed to assess significant differences among treatments at the p < 0.05 significance level. Origin 2021 software was used for graphing and correlation analysis.
3 Results
3.1 Effects of different carbon-based materials on salt leaching in the column experiment
3.1.1 Dynamics of cation leaching
Figure 2 illustrates the effects of applying carbon-based materials alone or in combination with flue FGD on the leaching concentrations of major cations (Na+, K+, Mg2+, and Ca2+) in the leachate. Significant differences in the concentrations of Na+, K+, Ca2+, and Mg2+ were observed among all treatments (Figures 2a–d). Compared to the control (CK), both carbon-based materials and FGD significantly enhanced Na+ leaching, with the co-application treatments showing superior effects to single applications. The CB+FGD co-application demonstrated the greatest efficacy, driving peak increases in leachate Na+ concentration of 114.19% and 97.33% compared to CK and BC, respectively. Na+ leaching predominantly occurred during the P1 (rapid decline) phase. Here, FGD alone and CB+FGD exhibited the most pronounced enhancement, increasing Na+ leaching by 89.08% and 90.92%, respectively, relative to CK. During the P2 (gradual decline) phase, leaching amounts for all treatments were significantly higher than CK, with CB+FGD showing the largest increase (101.37%). In the P3 (stable) phase, treatment differences were distinct, and CB+FGD increased Na+ leaching concentration by 226.23%.

Figure 2. The effects of carbon-based materials and their combined application of FGD on the main cations, such as Na+ (a), K+ (b), Ca2+ (c), and Mg2+ (d) in the eluent during the rinsing stages P1, P2 and P3. The error bar represents ± standard deviation, and different lowercase letters indicate significant differences in different treatments at the same rinsing stage (p < 0.05).
Application of CB alone and CB+FGD promoted K+ leaching compared to CK, increasing concentrations by 25.24% and 12.19%, respectively. Conversely, other treatments suppressed K+ leaching, indicating that FGD co-application reduced K+ concentration in the leachate. K+ leaching followed the order P1 > P2 > P3 across all phases. Both carbon-based materials and FGD enhanced Ca2+ leaching (co-application > single application), with CB+FGD showing the greatest increase (44.65%). Similarly, carbon-based materials and FGD significantly improved Mg2+ leaching compared to CK (single application > co-application). BC and BC+FGD treatments were most effective for Mg2+ leaching, achieving increases of 121.16% and 111.11% versus CK, respectively. Compared to sole FGD, these treatments showed significantly higher Mg2+ leaching rates (+32.70% and +26.67%, respectively). Leaching of Mg2+ induced by carbon-based materials primarily occurred during the P2 and P3 phases. Co-application with FGD reduced the Mg2+ leaching effect of CB in the CB+FGD treatment.
In summary, both carbon-based materials and FGD promoted the leaching of Na+, Ca2+, and Mg2+. However, FGD co-application specifically enhanced Na+ leaching while simultaneously suppressing the leaching of Ca2+, Mg2+, and K+. A decreasing trend in cation concentrations from the P1 to P3 phase suggests that the amendments alleviated salt stress in the saline soil.
3.1.2 Dynamics of anion leaching
Figure 3 shows the effects of different carbon-based materials and FGD co-application on the leaching concentrations of major anions (HCO3-, Cl-, and SO42-) in the leachate. Compared to CK, BC, FGD, and BC+FGD had no significant effect on HCO3- leaching. Sole CB application was most effective for HCO3- leaching, increasing leachate concentration by 144.81% and 98.85% compared to CK and BC. Conversely, FGD co-application reduced HCO3- concentration in the leachate, with CB+FGD showing the largest decrease (74.06%). HCO3- leaching was primarily concentrated in the P1 phase.

Figure 3. The effects of different carbon-based materials and their combined application of FGD on the main anions, such as HCO3- (a), Cl- (b), and SO42- (c) in the eluent during the rinsing stages P1, P2 and P3. The error bar represents ± standard deviation, and different lowercase letters indicate significant differences in different treatments at the same rinsing stage (p < 0.05).
All treatments significantly promoted the leaching of Cl- and SO42- compared to CK across all leaching phases (co-application > single application). CB+FGD was the most effective treatment, increasing Cl- and SO42- concentrations by 105.29% and 155.42%, respectively. Compared with CB, the increases of Cl- and SO42- reached 14.78% and 11.73%. These results indicate that the treatments facilitated anion leaching to varying degrees, thereby reducing the accumulation of harmful ions in the saline soil.
3.1.3 Post-leaching cation distribution in soil profile
Figure 4 depicts the effects of carbon-based materials and FGD co-application on the distribution of major cations (Na+, K+, Mg2+, Ca2+) within the soil profile after leaching. Application of carbon-based materials and FGD significantly reduced Na+ content in all soil layers (co-application > single application), with CB+FGD showing the maximum reduction (40.43%). Na+ content generally increased with soil depth, except in the BC treatment. Compared to CK, single application of carbon-based materials and FGD co-application significantly reduced K+ content in the 0–20 cm layer, with CB alone causing the largest decrease (38.81%). Single FGD application increased K+ content. BC and BC+FGD treatments resulted in significantly higher K+ content in the 20–30 cm layer compared to other treatments.

Figure 4. The effects of different carbon-based materials and their combined application of FGD on the main cations, such as Na+ (a), K+ (b), Ca2+ (c), and Mg2+ (d) in different soil layer profiles. The error bar represents ± standard deviation, and different lowercase letters indicate significant differences in different treatments at the same rinsing stage (p < 0.05).
Carbon-based materials and FGD significantly enhanced the retention of Ca2+ in the soil. Increases were particularly notable for FGD, BC+FGD, and CB+FGD treatments, and Ca2+ content generally increased with soil depth. Treatments other than CB and FGD alone reduced soil Mg2+ content compared to CK. FGD co-application had no significant impact on Mg2+ leaching. The highest Mg2+ content in the 0–20 cm and 20–30 cm layers was observed in the CB and FGD treatments, respectively.
3.1.4 Post-leaching anion distribution in soil profile
Figure 5 shows the effects of carbon-based materials and FGD co-application on the distribution of major anions (HCO3-, Cl-, SO42-) within the soil profile after leaching. FGD co-application significantly reduced soil HCO3- concentration. In the 0–20 cm layer, BC+FGD and CB+FGD treatments showed significant decreases (41.67% and 40.28%, respectively). In the 20–30 cm layer, CB+FGD caused the most significant reduction (13.16%). Carbon-based materials and FGD significantly decreased soil Cl- concentration compared to CK (co-application > single application), with CB+FGD being the most effective. Cl- content was markedly reduced in the 0–20 cm layer across treatments, while BC and FGD significantly increased Cl- in the 20–30 cm layer.

Figure 5. The effects of different carbon-based materials and their combined application of FGD on the main anions, such as HCO3- (a), Cl- (b), and SO42- (c) in different soil layer profiles. The error bar represents ± standard deviation, and different lowercase letters indicate significant differences among different treatments in the same soil layer (p< 0.05).
Both carbon-based materials and FGD reduced soil SO42- concentration (single application > co-application), with CB showing the largest decrease (30.33%). Single application of carbon-based materials had no significant effect on SO42- in the 0–20 cm layer, but significantly lowered its content compared to CK in the 20–30 cm layer.
3.2 Dynamics of salt ions in field soil
3.2.1 Dynamics of cations in field soil
Figure 6 illustrates the changes in major cations (Na+, K+, Mg2+, Ca2+) across different soil layers in saline soil treated with carbon-based materials and FGD co-application during various cotton growth stages. Compared to CK, the addition of carbon-based materials and FGD reduced Na+ and Mg2+ contents to varying degrees, while Ca2+ exhibited an opposite trend. K+ content in BC, CB, and CB+FGD treatments showed an increasing trend at different stages. With the exception of Na+, co-application with FGD generally led to increasing cation concentrations with soil depth. Na+ content in the 0–20 cm layer decreased significantly as the cotton growth progressed. FGD co-application significantly reduced Na+ content in all layers, with CB+FGD showing the largest reduction (37.90%). K+ content in all layers initially increased and then decreased during the cotton growth period. Adding CB (except at the seedling stage) resulted in higher K+ content than CK throughout the growth stages. FGD and BC+FGD treatments consistently had significantly lower K+ content than CK across all growth stages. Carbon-based materials and FGD significantly increased Ca2+ content in all soil layers during all growth stages (co-application > single application), with CB+FGD showing the maximum increase. Carbon-based materials maintained Mg2+ content below CK levels throughout the growth period, reaching its minimum at the boll-opening stage. Both FGD and CB+FGD reduced Mg2+ content by 11.77% compared to CK.

Figure 6. Effects of different carbon-based materials and their combined application of FGD on cations, such as Na+ (a), K+ (b), Ca2+ (c), and Mg2+ (d) in different soil layers. The error bar represents ± standard deviation, and different lowercase letters indicate significant differences in different treatments at the same rinsing stage (p < 0.05).
3.2.2 Dynamics of anions in field soil
Figure 7 shows the changes in major anions (HCO3-, Cl-, SO42-) across different soil layers in saline soil treated with carbon-based materials and FGD co-application during various cotton growth stages. Compared to CK, the amendments decreased HCO3- and Cl- contents to varying degrees, while SO42- showed an opposite trend. Except for SO42-- content decreased significantly as the cotton growth progressed, reaching its lowest level at the boll-opening stage. FGD co-application significantly reduced HCO3- content in the 0–20 cm layer, with CB+FGD showing the largest decrease. Cl- content in all layers showed an increasing trend during the growth period and increased significantly with soil depth. FGD co-application significantly reduced Cl- content in all layers of the saline soil, with CB+FGD again showing the largest reduction. Carbon-based materials and FGD significantly increased SO42- content in the saline soil (co-application > single application), with CB+FGD exhibiting the greatest increase. SO42- content decreased significantly as the cotton growth progressed but showed no clear trend with increasing soil depth.

Figure 7. Effects of different carbon-based materials and their combined application of FGD on anions, such as HCO3- (a), Cl- (b), and SO42- (c) in different soil layers. The error bar represents ± standard deviation, and different lowercase letters indicate significant differences in different treatments at the same rinsing stage (p < 0.05).
3.2.3 Dynamics of soil physicochemical properties
Application of carbon-based materials and FGD significantly improved soil properties in the 0–20 cm layer (Figure 8). These treatments significantly reduced TSS at the seedling stage, although the effect was less pronounced or non-significant in the subsequent three growth stages (Figure 8a). Single amendments generally led to larger TSS reductions than co-application treatments, with CB showing the highest decrease (14.15%), possibly due to the introduction of ions like Mg2+ and Ca2+ from FGD. TSS gradually decreased throughout the cotton growth period across all treatments. Soil EC, which was positively correlated with TSS, exhibited a similar decreasing trend over the growth period (Figure 8b). Compared to CK, carbon-based materials and FGD significantly reduced soil EC. However, EC values in FGD co-application treatments were consistently higher than those with single carbon-based material applications, and single FGD application resulted in the smallest EC reduction. The SAR, reflecting the soil’s capacity to counteract Na+ alkalinity with Ca2+ and Mg2+, was significantly lower in amended soils compared to CK (Figure 8c). Co-application effects were markedly superior to single applications. CB+FGD showed the largest SAR reduction, decreasing it by 34.74%, 31.61%, 38.15%, and 41.02% at the seedling, Bud, flowering and boll, and boll-opening stages, respectively.

Figure 8. Total dissolved salts (a), The electrical conductivity (EC) (b), sodium adsorption ratio (SAR) (c) and their correlation analysis in saline soil at different growth stages of cotton (d). The error bar represents ± standard deviation, and different lowercase letters indicate significant differences in different treatments at the same rinsing stage (p < 0.05).
Figure 8 also reflects the correlations between soil physicochemical indicators and salt ions. A highly significant positive correlation (R2 = 0.52, p < 0.01) was observed between EC and TSS, confirming EC as an indirect measure of soil salinity. Na+, Ca2+, Cl-, and SO42- showed highly significant positive correlations (p < 0.001) with TSS, identifying them as major contributors to salinity. SAR exhibited a strong positive correlation with Na+ (R2 = 0.98, p < 0.001) and significant negative correlations with Ca2+ (R2=-0.69, p < 0.01) and Mg2+ (R2=-0.58, p < 0.01). These results demonstrate the antagonistic role of Ca2+ and Mg2+ in countering Na+ toxicity. Reducing exchangeable Na+ while applying calcium-based amendments represents an effective saline-alkali soil reclamation strategy. HCO3- showed a weak negative correlation with SAR (p < 0.05), potentially due to reduced dissolved salt content from carbonate precipitation under alkaline conditions. K+ showed no significant correlation with salinity indicators, reflecting its tendency for adsorption or plant uptake and its low contribution to salt stress.
4 Discussion
4.1 Dynamics of salt ions in leachate
This study primarily investigated the effects of carbon-based materials and FGD on salt dynamics within the 0–30 cm profile of saline soil. The dominant ions contributing to salinity in the study area were Na+, Ca2+, Mg2+, SO42-, and Cl- (Table 1, Figure 8d). The application of carbon-based materials and FGD significantly enhanced the leaching of these salt ions (Figures 2, 3), consistent with findings from previous studies (25, 34). Co-application of carbon-based materials with flue FGD generally outperformed single applications in promoting ion leaching, resulting in higher cumulative amounts of dissolved Na+, Ca2+, SO42-, and Cl- in the leachate. The chitosan-modified superabsorbent carbon-based material co-applied with FGD (CB+FGD) exhibited the most pronounced effect, significantly enhancing the leaching of Na+, Ca2+, SO42-, and Cl- compared to other treatments. The overall leaching efficacy followed the order: co-application > single application > control (CK).
The porous structure and high specific surface area (SSA) of carbon-based materials facilitate the adsorption of salt ions within their pores, thereby reducing total soil salinity and promoting ion elution (35). Furthermore, they enhance soil aggregate formation and increase total porosity (18, 22, 36), improving the physical structure of saline-alkali soil. This modification increases the viscosity coefficient of the soil solution, retards water movement, and ultimately enhances salt leaching efficiency (30). The superabsorbent carbon-based material (CB), possessing a larger SSA and superior water absorption and retention capabilities (15), demonstrated more significant leaching effects (18, 19). Concurrently, Ca2+ and Mg2+ introduced by the carbon-based materials can displace exchangeable Na+ from soil colloids via cation exchange, further improving leaching efficiency (37).
Co-application with FGD augmented the leaching of Na+, Ca2+, and SO42- by the carbon-based materials. This co-application effect likely stems from the primary component of FGD, CaSO4·2H2O, which significantly increases soil Ca2+ and SO42- concentrations. Consequently, the leaching amounts of Ca2+ and SO42- in the leachate rise substantially. The additional Ca2+ also displaces exchangeable Na+ adsorbed onto soil colloids, further promoting Na+ leaching (38).
4.2 Distribution of salt ions in soil profile post-leaching
Removing major salt ions like Na+ and Cl- is crucial for ameliorating soil salinity. Both single and co-applications of carbon-based materials and FGD effectively reduced Na+ content in the saline soil, with co-application proving superior. The CB+FGD treatment exhibited the strongest Na+ suppression effect (Figure 4). This can be attributed to the porous structure and high SSA of carbon-based materials enabling effective adsorption of Na+ (31). The CB, while retaining the inherent porous structure, significantly increases SSA (15), thereby enhancing Na+ adsorption. Its improved water retention capacity also accelerates salt leaching (35). FGD provides supplemental Ca2+ to displace Na+ from soil exchange sites (38).
FGD application significantly increased soil Ca2+ concentration. However, BC+FGD and CB+FGD co-applications showed no significant difference in Ca2+ and Mg2+ content compared to FGD alone, suggesting that Ca2+ and Mg2+ dynamics are primarily governed by FGD application (39, 40). Biochar and FGD supply polyvalent cations (e.g., Ca2+ and Mg2+) and anions (e.g., SO42) (1, 2), which promote soil aggregate formation and soluble MgSO4 generation (34). This enhances soil permeability and Mg2+ mobility, ultimately increasing leaching losses (21, 22). However, when co-applied with biochar, FGD’s Mg2+-mobilizing effect is significantly attenuated (30). Biochar achieves this by adsorbing/immobilizing Mg2+ ions and inducing precipitation through pH modification (23, 35). BC and BC+FGD treatments resulted in higher soil K+ levels than others, likely due to the inherent K+ content of the biochar feedstock. Nevertheless, the porous structure of biochar can promote K+ leaching, explaining the significantly higher K+ content observed in the 20–30 cm layer compared to 0–20 cm. While Na+ concentration decreased and Ca2+ and K+ concentrations increased overall, all three ions generally exhibited higher concentrations with increasing soil depth. This indicates that the amendments effectively modulated salt distribution within the profile. Irrigation during the crop growth period aids in leaching salts from the soil surface, representing a primary desalination phase in arid farmland (41). Our findings align with studies showing biochar enhances water retention and reduces salinity in the 0–40 cm layer (27), and that straw interlayers improve leaching efficiency by reducing infiltration rates (42).
The test soil was classified as chloride-sulfate saline soil (43). After leaching, Cl- content was significantly reduced in the 0–20 cm layer, with CB+FGD showing the largest decrease. Conversely, FGD, BC+FGD, and CB+FGD treatments increased SO42- content, potentially transforming the topsoil (0–20 cm) towards sulfate dominance. This demonstrates that both amendments promote Cl- leaching (25, 44). The significant increase in Cl- within the 20–30 cm layer (Figure 5) indicates downward migration of surface Cl- with percolating water, increasing salinity in the subsoil (27). Extensive research confirms that carbon-based materials possess lower bulk density and more developed pore structures than saline soils. By enhancing soil water content and infiltration capacity, they accelerate desalination (7, 35, 45). The chitosan-modified CB, containing more hydrophilic functional groups and exhibiting better hydrophilicity and polarity, increased soil water retention capacity by 23% compared to BC (15), contributing to its higher desalination efficiency.
While co-application increased SO42- leaching, it also elevated SO42- content in the post-leaching soil. This shift from potentially harmful carbonates and bicarbonates to less detrimental sulfates can be beneficial (39). FGD co-application significantly reduced HCO3- in the 0–20 cm layer but led to its accumulation in the 20–30 cm layer. This phenomenon may relate to the precipitation-dissolution equilibrium of CaCO3, soil ion adsorption, exchange equilibria, and the decomposition of carbonate minerals to maintain electrostatic equilibrium (40). In summary, the application of carbon-based materials, particularly the chitosan-modified CB, significantly improved the physicochemical properties of the topsoil. By reducing harmful ions (Na+, Cl-) and increasing beneficial ions for plant growth (K+, Ca2+, SO42-), it mitigated salt accumulation in the surface layer.
4.3 Dynamics of salt ions in field soil
Soil salinity is a major environmental factor influencing crop growth, directly impacting seedling emergence, plant development, and ultimately yield (7). Field trial results showed that Na+ content decreased progressively during the cotton growth period but increased with soil depth. Ca2+ content also decreased over time, potentially linked to cotton root uptake for cell wall synthesis and osmotic regulation (46). Co-application outperformed single applications in maintaining Ca2+ availability; FGD provides a sustained Ca2+ release, while surface functional groups (e.g., carboxyl, hydroxyl) on the carbon-based materials reduce Ca2+ leaching to deeper layers via electrostatic adsorption, preserving its effectiveness in the topsoil (1). HCO3- content reached its minimum at the boll-opening stage, possibly due to reduced evaporation shifting the carbonate system equilibrium towards CO2 release (47). Cl- content in the 0–20 cm layer increased during the growth period and rose significantly with depth. Both amendments significantly increased SO42- content, with CB+FGD showing the largest increase, consistent with the leaching experiment results. This pattern confirms that irrigation inputs during cotton growth drive the downward migration of surface salts with percolating water (41).
Co-application treatments consistently maintained lower Na+ and Cl- content across all soil layers and growth stages compared to single applications. Ca2+ supplied by FGD displaces Na+ from soil colloids via ion exchange (38), reducing soil sodium saturation and enhancing permeability. This facilitates the leaching of ions with water towards deeper soil layers (41). The co-application effect of carbon-based materials and FGD was particularly pronounced in the topsoil (0–20 cm), potentially linked to biochemical processes in the root-dense zone, such as root exudates activating functional groups on the carbon materials (26). The CB, functioning as a soil amendment, contains a higher density of hydrophilic and cation-binding groups (e.g., carbonyl, hydroxyl, quaternary ammonium) (19) and exhibits exceptional water absorption and retention properties (15). These characteristics synergistically enhance salt ion leaching efficiency.
As the cotton grew and fertilization proceeded, soil K+ content increased notably. The abundant hydroxyl groups on the polymer network of the superabsorbent CB can release H+ (15), displacing and adsorbing K+ from the soil solution. This sequesters K+ within the material’s surface and internal structure, reducing its loss and promoting retention. Concurrently, the improved soil moisture environment fostered by CB application enhanced cotton growth and root development. Increasing root exudates likely stimulated the release of slow-release or insoluble potassium into the soil solution, contributing to the rise in K+ (19). Furthermore, most Na+ and K+ in the soil exist in free ionic forms (45), and an antagonistic relationship exists between them (48). Their absolute and relative quantities exhibited opposing trends over time, persisting until the end of the cotton growth period. The superabsorbent CB can reduce pore water salinity by binding salt ions within its polymeric chain structure, thereby mitigating salt ion accumulation and their detrimental effects on crops. Additionally, sole reliance on FGD for reclamation can lead to seasonal fluctuations in salinity. During high-temperature periods with low soil moisture, weak leaching, and strong evaporation, salt ions migrate upwards with evaporating water, causing surface salt accumulation. The superabsorbent CB counters this by enhancing soil water retention, improving water use efficiency, and suppressing evaporation. This effectively inhibits seasonal salt resurfacing and reduces harmful ion concentrations in the topsoil. Therefore, the co-application of superabsorbent carbon-based material and FGD is advantageous for reclaiming saline cotton fields and promoting sustainable agriculture in arid and semi-arid regions.
4.4 Dynamics of soil physicochemical properties
Salinity directly affects soil nutrient availability and crop growth (14). The highly significant positive correlation (p < 0.01) between TSS and EC confirms their mutual utility in characterizing soil salinity, with EC serving as a reliable rapid indicator (7). The significant reduction in TSS at the seedling stage by carbon-based materials and FGD is closely linked to the strong adsorption capacity and ion exchange functionality of the carbon materials (15). The single CB application showed the largest TSS decrease. In co-application treatments, the carbon material may buffer the rapid dissolution of FGD, delaying salt release and resulting in a relatively smaller TSS reduction (25). The TSS reduction from single FGD application was lower than from single carbon material application, likely because Ca2+ and Mg2+ released from dissolving FGD displace adsorbed Na+ but simultaneously increase SO42- content (38). The decrease in TSS and EC over the growth period is likely attributable to salt leaching induced by irrigation or precipitation (30). Other studies also report negative correlations between soil TSS/EC and biochar application (10, 25).
The significant reduction in SAR observed in the co-application treatment (CB+FGD) provides key evidence for the reduced effect of sodicity risk by carbon-based materials and FGD. The strong positive correlations (p < 0.001) of Na+, Ca2+, Cl-, and SO42- with TSS identify them as the primary contributors to salinity. The strong positive correlation between SAR and Na+, coupled with negative correlations with Ca2+ and Mg2+, confirms the antagonistic role of Ca2+ and Mg2+ in counteracting Na+ toxicity. The lack of significant correlation between K+ and salinity indicators suggests that K+ is primarily adsorbed or preferentially taken up by plants, contributing to osmotic adjustment rather than exacerbating soil salt stress (10). This study elucidates the mechanisms by which carbon-based materials and FGD achieve efficient amelioration of the 0–20 cm soil layer through regulating key ion balances and soil solution chemistry. Future research should investigate the long-term effects of these amendments on soil microbial communities, nutrient cycling, and plant physiology to refine the theoretical framework for saline soil ecological restoration.
5 Conclusion
This study investigated the ameliorative effects of co-applying a superabsorbent carbon-based material with FGD on saline-alkali soil. The results demonstrate that the application of carbon-based materials and FGD significantly enhanced salt ion leaching, effectively mitigating salt stress in saline soils of arid and semi-arid regions. The CB+FGD co-application treatment proved most effective, significantly reducing Na+ and Cl- content, increasing concentrations of K+, Ca2+, and SO42-, and reducing salt accumulation in the topsoil.
1. Co-application of the superabsorbent carbon-based material and FGD significantly alleviated salt stress by promoting Na+ leaching (co-application > single application). During the P1 (rapid decline) leaching phase, FGD alone and CB+FGD increased Na+ leaching concentration by 89.08% and 90.92%, respectively. FGD co-application significantly increased soil Ca2+ and SO42- content. The superabsorbent carbon-based material effectively retained soil K+, and post-leaching Cl- content was significantly lower than in the CK.
2. Field trials further confirmed that co-application of the superabsorbent carbon-based material and FGD significantly reduced Na+, Cl-, and Mg2+ content while increasing Ca2+, K+, and SO42- content. The increasing concentrations of Na+, Cl-, and K+ with soil depth indicate the migration of salts towards deeper soil layers with water movement.
3. The CB+FGD treatment significantly reduced TSS, EC, and SAR, thereby improving key physicochemical properties of the saline soil.
These results provide a scientific basis for optimizing the application of CB and FGD in saline-alkali soil remediation. Future studies should integrate long-term monitoring of multi-dimensional soil indicators (physical, chemical, and biological), coupled with plant physiological responses, to comprehensively elucidate the mechanisms and sustainability of CB-FGD co-application under field conditions.
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding author.
Author contributions
SZ: Writing – original draft, Methodology, Conceptualization. YY: Writing – original draft. JZ: Formal Analysis, Visualization, Writing – review & editing, Funding acquisition. XQ: Writing – review & editing, Data curation.
Funding
The author(s) declare that financial support was received for the research and/or publication of this article. This work was supported by the National Natural Science Foundation of China (42275014; 51569030), Bingtuan Guiding Science and Technology Plan Program (2024ZD098), President’s foundation of Tarim University (TDZKCX202404, TDZKSS202156), and Bingtuan Science and Technology Program (2021DB019; 2022CB001-01; 20240231).
Acknowledgments
We gratefully acknowledge the support of the Instrumental Analysis Center in Tarim University.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Generative AI statement
The author(s) declare that no Generative AI was used in the creation of this manuscript.
Publisher’s note
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Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fsoil.2025.1639967/full#supplementary-material
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Keywords: saline-alkali soil, superabsorbent carbon-based material, flue gas desulfurization gypsum (FGD), salt suppression, leaching efficiency
Citation: Zhang S, Yang Y, Zhang J and Qian X (2025) Mitigating salt stress in saline-alkali soils through co-application of superabsorbent carbon-based material and flue gas desulfurization gypsum. Front. Soil Sci. 5:1639967. doi: 10.3389/fsoil.2025.1639967
Received: 03 June 2025; Accepted: 23 June 2025;
Published: 10 July 2025.
Edited by:
Xinqiang Liang, Zhejiang University, ChinaCopyright © 2025 Zhang, Yang, Zhang and Qian. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Xiaoyan Qian, MTc2MTIyNDc0ODRAMTYzLmNvbQ==