Preparation and properties of hydrogel based on sawdust cellulose for environmentally friendly slow release fertilizers

Abstract A novel hydrogel slow-release nitrogen fertilizer based on sawdust with water absorbency was prepared using grafting copolymerization. Urea was incorporated as nitrogen source in a hydrogel fertilizer. Potassium persulfate (KPS) and N,N᾽-methylenebis acrylamide (MBA) were used as the initiator and cross-linker, respectively. The structure and properties of the samples were characterized by XPS, EDS, SEM, XRD and FTIR. The effects of various salt solutions, ionic strength and pH on swelling behavior were discussed. The results showed that the largest water absorbency of the sample reached 210 g/g in distilled water. In addition, the sample had the good nitrogen release property. Thus, the novel environmentally friendly hydrogel fertilizer may be widely applied to agricultural and horticultural fields.


Introduction
Let F denote a eld and let V denote a vector space over F with nite positive dim pair A, A * of diagonalizable F-linear maps on V, each of which acts on an eigenbasis irreducible tridiagonal fashion. Such a pair is called a Leonard pair (see [13, De nition A, A * is said to be self-dual whenever there exists an automorphism of the endomorp swaps A and A * . In this case such an automorphism is unique, and called the duality The literature contains many examples of self-dual Leonard pairs. For instance (i) th ated with an irreducible module for the Terwilliger algebra of the hypercube (see [4, Cor Leonard pair of Krawtchouk type (see [10, De nition 6.1]); (iii) the Leonard pair associa module for the Terwilliger algebra of a distance-regular graph that has a spin model in bra (see [1,Theorem], [3,Theorems 4.1,5.5]); (iv) an appropriately normalized totally (see [11,Lemma 14.8]); (v) the Leonard pair consisting of any two of a modular Leonar De nition 1.4]); (vi) the Leonard pair consisting of a pair of opposite generators for t bra, acting on an evaluation module (see [5,Proposition 9.2]). The example (i) is a spec examples (iii), (iv) are special cases of (v).
Let A, A * denote a Leonard pair on V. We can determine whether A, A * is self-dua By [ Then A, A * is self-du is a standard ordering of the eigenvalues of A * (see [7,Proposition 8.7]). factors affecting agricultural production, so it is very important to improve utilization of fertilizer nutrient and water resources [2][3][4]. Urea is the most widely used nitrogen fertilizer which has a high nitrogen content and low production cost. However, urea released rapidly in a short time in soil [5][6][7]. Volatilization, leaching, and runoff of nutrients caused waste of fertilizers and contamination of water [8]. With the reduction of freshwater resources, irrigation water sources also are deficient. Therefore, it was very important to establish a reasonable water and fertilizer system.
The hydrogel is a superabsorbent polymer with a three-dimensional network structure. Hydrogel can absorb large amounts of liquids, which can weigh dozens or even hundreds of times their own weight [9]. Because of the strong water absorbency of hydrogel, it have been widely used to be water-retaining materials [10,11]. The hydrogel slow-release fertilizer (HSRF) is a multifunctional fertilizer, which can not only improve the utilization rate of fertilizer, and reduce the harm to the environment, but also maintain the soil moisture [12]. HSRF has excellent water retention, and effectively reduces irrigation frequency and production costs. At the same time, based on the slow release characteristics of HSRF, the mortality of plants reduced and the utilization rate of fertilizer was improved [13,14]. Fertilizer can be loaded into the hydrogel by many techniques, two methods were most commonly used: one is that the fertilizers are directly grafted on the hydrogel polymer chains, and the other one is that the hydrogel is first synthesized, and then the hydrogel is immersed in the fertilizers solution until it is saturated [14]. However, the application of hydrogel has encountered some problems in agricultural fields. Traditional hydrogel was synthesized from acrylic acid (AA) and acrylamide (AM). AA and AM were expensive and had poor degradation performance, which was not suitable for the sustainable development of green agriculture [15]. Therefore, some researchers have proposed to use bio-materials to synthesize hydrogel, such as starch [16,17], wheat straw [13,17,18], pineapple peel [19], leftover rice [20], corncob [8], flax yarn waste [9], chicken gelatin [21], yeast [22], methyl chitosan [23], cotton stalk [4,8], mulberry branch [24], cellulose acetate [25] and so on. Sawdust is a renewable and environmentally friendly biomass resource, which contain 61.2% cellulose [26][27][28]. However, most of sawdust was burnt, and the residual value of sawdust cannot be fully utilized [29]. As far as we know, there were no reports with the application of sawdust in hydrogel fertilizers fields. Therefore, we tried to use sawdust to prepare HSRF, thereby improving water absorption and fertilizer utilization to develop the environment-friendly agriculture.
The aim of this work is to synthesize a HSRF based on sawdust, AA, AM, and urea. The structure and properties of HSRF were characterized by using FTIR, XRD, SEM, XPS, EDS and TGA. In addition, water holding capacity, water absorbency capacity, nitrogen release behavior, swelling kinetics and release kinetics of the sample were also investigated systematically.

Materials
Sawdust was provided by Sanyou Furniture Factory. Sodium hydroxide, N,N᾽-methylenebis acrylamide (MBA), potassium persulfate (KPS), hydrochloric acid and ethyl alcohol were obtained from Kaitong Chemical Reagent Co., Ltd. (Tianjin, China). Acrylic acid monomer (AA) and acrylamide (AM) were purchased from Macklin Chemical Reagents Co., Ltd. (Shanghai, China). Urea particles were obtained from Lanhua Coal Mining Group Co., Ltd. (Shanxi, China). Deionized water was used throughout the experiment. All reagents were of analytical reagent grade or commercial purity and were easily obtained from commercial sources.

Preparation of sawdust cellulose (SC)
First of all, the sawdust was washed and dried, then crushed and sieved (100 mesh). The sawdust powder was immersed in 10 wt% ammonia solution for 48 h and the mass ratio of sawdust powder to 10 wt% ammonia solution was 1:12, then the sawdust powder was filtered and washed with deionized water until the washing water was clean. Then, the sawdust powder was dried at 70°C in a drying oven. Next, the sawdust powder was put in 1 mol/L nitric acid and boiled for 45 min, and the mass ratio of sawdust to nitric acid was 1:12. And the sawdust powder was filtered and washed by using the same method until the pH of washing water was 7. After the samples were dried, the sawdust cellulose were obtained [17].

Preparation of HSRF
2 g sodium hydroxide was dissolved in 30 mL deionized water and the mixed solution was added to a 250 mL flask equipped with a mechanical stirrer. The flask was put in a water bath to make sure constant condition of 70°C. Then, 6 g AA, 3 g AM, 2 g urea and 0.07 g MBA were added to the flask. Next, flask was purged with nitrogen until the reaction completed. After stirring for 15 min, the mixed solutions (30 mL deionized water, 1 g sawdust cellulose and 0.15 g KPS) were added into the above-mentioned flask. The water bath was kept at 70°C and stirred continuously for 4 h to complete the polymerization process. After the polymerization reaction completed, the sample was washed with ethanol to remove unreacted parts. At last, the HSRF was cut into small pieces (2 × 2 mm) and placed in a drying oven at 70°C to constant weight and stored for future use. The mechanism of the polymerization is shown in Scheme 1. The preparation process of SC-g-PAA/ PAM/Urea is shown in Scheme 2.

Characterization
The FTIR spectra of samples were analyzed by singusing a Nicolet 380 FTIR spectrometer. The samples were subjected to wave numbers within the range of 500 to 4000 cm −1 at a resolution of 4 cm −1 . The thermal stability of the various samples were evaluated under N 2 circumstance by thermo-gravimetric analysis (TGA, DTG60A, Japan), the temperature was heated from 20°C to 800°C at a rate of 10°C/min. The morphologies of samples were analyzed by scanning electron microscopy (SEM, JSM-5800, Japan). The surface elemental composition and distribution of the samples were observed by X-ray photoelectron spectrometer (XPS, Escalab 250Xi, America) and Energy dispersive spectrometer (EDS). The X-ray diffracion(XRD) measurements were couducted by an X-ray diffractometer (XRD, D8 Advance, Germany).

Swelling capacity and kinetics
0.2 g of the dried sample was immersed in 150 mL of deionized water and NaCl solution (1.0 wt%), respectively, which were allowed to absorb solution until swelling equilibrium was obtained. Then, the swollen samples were quickly separated from the solution and measured the weight of the HSRF. The equilibrium water absorbency Q eq (g/g) was calculated using Eq. 1: where W 1 (g) and W 0 (g) represented the weight of swollen and dried samples, respectively. Q eq (g/g) indicated the weight of absorbed solution.
In order to study the effect of pH on the water absorbency of samples, the different pH solutions were used as soaking media. Various pH solutions were prepared by NaOH (0.1 mol/L) and HCl (0.1 mol/L) aqueous solutions. The Q eq of samples in different pH solutions was determined by the same method.
To study the swelling kinetics of samples in various saline solutions, 10 mmol/L NaCl, CaCl 2 , KCl, MgCl 2 , and NH 4 Cl solutions were prepared, respectively. Specific steps were as follows: 0.5 g of dried samples were put in nylon bags, which were immersed in the different salt solutions.
In order to further study the swelling kinetics of samples in water, schott's second-order swelling kinetics model can be indicated by the following equation: where Q t (g/g) was the water absorbency at any time t; Q m (g/g) was the theoretical equilibrium water absorbency; K is was the swelling rate constant.

Measurement of the water-holding of SC-g-PAA/PAM/Urea in soil
1, 2, 3, 4 g SC-g-PAA/PAM/Urea were mixed with 200 g of dry soil (20 mesh, the ratio of soil to sand was approximately 9:1) and placed in a 4.5 cm diameter polyvinyl chloride (PVC) tube, respectively. The bottom of the tube was sealed with nylon mesh and weighed (W 0 ). The tap water was poured slowly into the soil from the top of the tube until the water seeped out from the bottom and weighed (W 1 ). A control experiment without the SC-g-PAA/PAM/Urea was prepared by the same method. The water holding (WH%) in the soil was calculated using the following equation:

Release behavior and kinetics of SC-g-PAA/PAM/Urea in water
1 g of SC-g-PAA/PAM/Urea was placed in a nylon mesh bag and immersed in 200 mL of deionized water. The bags were removed from the glass bottle within the specified time intervals (1, 3, 5, 10, 15, 20, 30, 45, 60, 90, 120, 180, 240, 360, and 480 min). Approximately 2 mL of solution was drawn out from the glass bottle to detect the nutrient release of nitrogen using a UV-2450 spectrophotometer. All samples were measured in triplicate, and the results were the average value for each sample. The N contentration was calculated using the paradimethyl-amino-benzaldehyde colorimetry. First, 2 mL fertilizer extract solution was placed in a 25 mL colorimetric tube. Then, 20 mL of the 20 g/L para-dimethyl-aminobenzaldehyde solution and 2 mL of the 2 mol/L H 2 SO 4 solution were added. At last, 1 mL deionized water was added into the solution. The colorimetric tube was shaken to make solution even, and allow to stand for 15 min using the spectrophotometer at 422 nm wavelength to determine N contentration [18].
In order to further study the release kinetics and mechanism of HSRF in water, Ritger-Peppas release model was employed.
where M t and M ∞ were the cumulative fertilizer nutrients release at time t and infinite time, K was the release rate constant, t was the release time and n was the diffusional exponent. When n ≤ 0.45, the release mechanism belongs to Fick diffusion; when 0.45 < n < 0.89, for anomalous transport; when n ≥ 0.89, it indicates the Case II release mechanism, erosion mechanism for the skeleton [8,30,31].
The equation is suitable for the first 60% of the fractional nutrient release curves [32].

FTIR spectra
The FTIR spectra of the SC, AA, AM, urea and SC-g-PAA/ PAM/Urea were displayed in Figure 1. For the spectrum of SC, the characteristic peaks at 3426 and 2923 cm −1 were contributed to the -OH and C-H stretching vibration, respectively. And the peaks at 1386 and 1039 cm −1 were attributed to C-C and C-O-C stretching vibration. For the spectrum of AA, the intense bands were observed at 1715 and 1627 cm −1 , corresponding to the C=O stretching of -COOH and C=C groups, respectively. And there was a peak at 1434 cm −1 , which was assigned to symmetric stretching vibration of -COO − groups [33,34].  AM at 1678 cm −1 and the C=O stretching of -COOH groups of AA at 1715 cm −1 shifted to 1683 cm −1 in the FTIR spectrum of SC-g-PAA/PAM/Urea, signifying that intermolecular hydrogen-bonding interactions were created between -COOH and C=O groups during the polymerization process [8,23,35]. In addition, the characteristic urea bands at 3180 cm −1 with slight shifts, which is the stretching vibration of −NH 2 in −CONH 2 , and 570 cm −1 (bending vibration of N-CO-N) were visible, suggesting the involvement of urea in the SC-g-PAA/PAM/Urea [20,24,36]. The above analysis of FTIR information concluded that SC-g-PAA/PAM/Urea hydrogel fertilizer was successfully synthesized by using simple reactive methods.

X-ray diffraction analysis
X-ray diffraction analysis was intensively applied as a technique for quantifying the crystalline structure of polymer. Figure 2 exhibits the XRD patterns of SC-g-PAA/ PAM/Urea, SC and urea. For the SC, the peaks at 2θ = 15.8°, 22.3° and 2θ = 34.6°, corresponded to the characteristic crystalline peaks of cellulose I in nature [19]. The urea XRD patterns showed many characteristic reflections at 2θ = 22.3°, 24.6°, 29.4°, 31.7°, 35.5°, and 2θ = 37.1°, indicating that urea had a crystalline structure [20]. However, unlike urea and SC, SC-g-PAA/PAM/Urea exhibits a broader and larger peak. The absence of characteristic peaks of urea and SC for the SC-g-PAA/PAM/Urea, indicated that urea and SC had a amorphous structure in the hydrogel fertilizer [20,37] Additionally, the hydrogel fertilizer formed a amorphous structure by crosslinking of SC and urea. Therefore, SC and urea were successfully incorporated in the hydrogel fertilizer. Similar phenomena have been observed by wen et al. that reported the corncob-based hydrogel fertilizers [8].

XPS analysis
The chemical environment of carbon, nitrogen and oxygen atoms in urea and SC-g-PAA/PAM/Urea were studied by XPS. The O 1s (532.71 eV), N 1s (397.93 eV) and C 1s (284.65 eV) on the XPS spectrum of SC-g-PAA/PAM/Urea can be observed in subfigures A1-A3 of Figure 3. The O 1s (529.78 eV), N 1s (399.83 eV) and C 1s (286.89 eV) on the XPS spectrum of urea can be observed in subfigures B1-B3 of Figure 3. The C1s spectra can be fitted with four peaks at banding energies of 284.72, 286.14, 287.91 and 288.83 eV. The four peaks originated from C-C, C-N, C=O and O-C=O groups, respectively. Compared with the XPS spectrum of SC-g-PAA/PAM/Urea, the C1s of urea can be fitted to three peaks (subfigure B2 of Figure 3). The peaks at 284.73, 286.66 and 288.78 eV were attributed to C-C, C-N and C=O, respectively. The binding energy and atomic percentage were depicted in Table 1. Notably, the carbon atomic concentration and oxygen atomic concentration was increased significantly in the SC-g-PAA/PAM/Urea compared with urea. This change was attributed to the large amount of oxygen atoms and carbon atoms in the sawdust cellulose, and sawdust cellulose was successfully incorporated into the SC-g-PAA/PAM/Urea system.

Micro-morphology
The surface elemental composition and distribution of SC-g-PAA/PAM/Urea were displayed in the EDS spectra ( Figure 4a) and map (Figure 4c). Table 2 displays the quantitative analysis of the elements present in the EDS map. For the surfaces of SC-g-PAA/PAM/Urea, the uniform distributions of C, N, O, Na, K and P elements can be clearly observed. Furthermore, the abundant elements included by the SC-g-PAA/PAM/Urea could be applied to soil and then promoted to improve soil fertility and plant growth [8].
The surface microscopic morphology of SC and SC-g-PAA/PAM/Urea were observed in Figure 5. The SC exhibits block or rod-like morphology. Compared with that of SC, the coarse and fluffy surface was observed in the micrograph of SC-g-PAA/PAM/Urea. Additionally, few urea crystals (white spot) were dispersed on the surface of SC-g-PAA/PAM/Urea in Figure 5b. Similar phenomena have been reported by other researchers [20,34].

TGA analysis
TGA was conducted in order to evaluate the thermal stability property of different hydrogel fertilizers in Figure 6. TGA curves of different hydrogel fertilizers exhibit the obvious differences at elevated temperature. The TGA curves of SC-g-PAA/PAM/Urea shows three main thermal degradation stages. The first stage from 200°C to 320°C, it corresponded to the disintegration of branches or side chain groups of the polymer [36,38,39]. The second weight loss occurred within 320-520°C, it could be attributed to the decomposition of main chains of graft copolymer. Finally, the weight loss took place in the range of 520-800°C, it may be the further decomposition of residual organic matter [38,39]. SC-g-PAA/PAM, SC-g-PAA/Urea and PAA/PAM/Urea shows four main thermal degradation stages, respectively. Notably, the SC-g-PAA/PAM/Urea  had higher thermal stability than SC-g-PAA/PAM, SC-g-PAA/Urea and PAA/PAM/Urea. When the temperature was 550°C, the mass ratios of PAA/PAM/Urea, SC-g-PAA/Urea, SC-g-PAA/PAM and SC-g-PAA/PAM/Urea were 10.3%, 26.7%, 37.7%, 41.2%, respectively. Similar phenomena have been reported by Wen et al. [8]. Table 3 exhibits the main thermal properties for SC-g-PAA/PAM/ Urea and SC-g-PAA/PAM, SC-g-PAA/Urea and PAA/PAM/ Urea. It was noted that the 5% weight loss temperature (T 5% ), T 20% and T 50% in the SC-g-PAA/PAM/Urea had higher values than those of SC-g-PAA/PAM, SC-g-PAA/ Urea and PAA/PAM/Urea. Due to the introducing of SC, AA, urea, and AM in hydrogel system, chemical reactions among the molecular chains leaded to the formation of the highly dense network structure in hydrogel, then improving the thermal property of SC-g-PAA/PAM/Urea.

Water-holding capacity of soil with SC-g-PAA/PAM/Urea
The water-holding capacity of soil with SC-g-PAA/PAM/ Urea was displayed in Figure 7. For the soils mixed with different contents SC-g-PAA/PAM/Urea, soil mixed with 4 g samples had the largest water-holding ratios (161.2%), which was higher 122.5% than that of the soil without hydrogel sample (38.7%). It indicated that SC-g-PAA/PAM/Urea had excellent water-holding capacity.
The reason can be that the SC, AA and AM formed skeleton structure by polymerization [40,41]. And the introduction of the SC added the reactive molecular chains length, then increasing water absorption. Simultaneously, the incorporation of SC increased reactive nodes, easily forming skeleton structure. Therefore, the addition of SC can improve water-holding capacity of sample. Furthermore, It was observed that the maximum water-holding capacity would increase with the increase of SC-g-PAA/PAM/Urea dosage in the soil. The higher water-holding capacity can be attributed to the presence of a lot of hydrophilic groups in SC-g-PAA/PAM/Urea [8,41]. Therefore, the SC-g-PAA/ PAM/Urea was applied to the soil, the soil can hold a lot of water during irrigation or rain periods [40]. As a result, application of SC-g-PAA/PAM/Urea fertilizer can effectively reduce irrigation times and improve soil moisture. Additionally, SC-g-PAA/PAM/Urea also releases nutrients and increases crop yields.

Effect of salt solution on water absorbency of SC-g-PAA/PAM/Urea
The swelling curves of SC-g-PAA/PAM/Urea was displayed Figure 8. As can be seen from the figure, the water absorbency of SC-g-PAA/PAM/Urea in 0.01 mol/L NaCl was 108 g/g. However, the water absorbency of the SC-g-PAA/PAM/Urea in 0.50 mol/L NaCl was only 19.4 g/g.  As evident, the water absorbency of the SC-g-PAA/PAM/ Urea was inversely proportional to the concentration of the sodium chloride solution. This result was attributed to the decreased osmotic pressure difference with increasing saline solution concentration [8,38,42]. The osmotic pressure difference acted as a driving force at water absorbency stage of SC-g-PAA/PAM/Urea [42]. The higher concentration of solution would lead to a lower water absorbency driving force [38]. Therefore, SC-g-PAA/PAM/ Urea has strong water absorbency in low concentration NaCl solution.

Swelling capacity and kinetics
The effects of different saline solutions on the water absorbency of the SC-g-PAA/PAM/Urea were illustrated in Figure 9a. As shown in Figure 9a, the SC-g-PAA/PAM/ Urea had the highest water absorbency in NaCl solution and the lowest water absorbency in CaCl 2 solution. As evident, in the same concentration of salt solution, the water absorbency of the SC-g-PAA/PAM/Urea decreased with the increase of cationic charges. The result was similar to that of LR-PAA/MMT/Urea reported by Zhou et al. [20]. The water absorbency of the SC-g-PAA/PAM/ Urea in 0.01 mol/L saline solutions was in the order of Na + > K + > NH 4 + > Mg 2+ > Ca 2+ . This result was attributed to the formation of complexs by the -COO − groups with multivalent cations, which increased the crosslink density of the hydrogel network [20]. In addition, multivalent cations have higher ionic strength than monovalent cations, so hydrogels had low water absorbency in multivalent cations solutions. Moreover, the smaller radius of the cations were corresponded to the stronger water absorbency capacity of the hydrogel (Na + > K + > Mg 2+ > Ca 2+ ). Figure 9b shows the swelling kinetics of the sample. The Q m and K is , and the correlation coefficients (R 2 ) were listed in Table 4. The plots revealed lines with good linear correlation coefficient, the Q m of the swelling kinetics model was close to the experimental value, it was indicated that the Schott's second-orderkinetic model can be applied for the swelling process of the SC-g-PAA/PAM/Urea [17,20,32]. It can be seen from the figure that the less the water absorbency, the less the Q m value. The swelling rate of the sample was mainly related to the osmotic pressure of the immersed medium and the relaxation rate of the chain segments in the network.

Effect of pH on water absorbency of SC-g-PAA/PAM/Urea
The swelling behavior of the SC-g-PAA/PAM/Urea was investigated in various solutions with different pH   values ranging from 2 to 12. Figure 10 shows the effect of pH on water absorbency of SC-g-PAA/PAM/Urea. The water absorbency of SC-g-PAA/PAM/Urea increased with the pH from 2 to 7. In the case of a solution with a strong acidity most -COO − was protonated and converted to -COOH. In addition, the hydrogen bonds between -COOH was strengthened by the protonation of -COO − . These results restrained the anion-anion electrostatic repulsion, so decreased the swelling capacity of SC-g-PAA/PAM/Urea at the acidic pH [8,17,33]. With the pH of the solution increased, some -COOH groups were ionized and converted to -COO − [8]. At the same time, the hydrogen bonds between -COOH was weakened, the electrostatic repulsion between -COO − was enhanced, and the water absorbency was increased. At a pH of 7, the water absorbency reached a maximum [8,17,33]. The water absorbency of the SC-g-PAA/PAM/Urea decreased with the pH from 8 to 12. This result was attributed to the Na + screening effect. The anion-anion electrostatic repulsion was decreased with the alkalinity of the solution increase and the concentration increase of Na + [43,44]. Therefore, the water absorbency of the SC-g-PAA/PAM/ Urea was reduced.     Figure 11a indicates nutrient release ability of SC-g-PAA/ PAM/Urea at 25°C in water. The cumulative nutrient release of SC-g-PAA/PAM/Urea was 2.6%, 8.6%, and 82.4% within 10, 30, and 480 min, respectively. It could be found that the initial release rate of nitrogen was slow, and then gradually increased. Finally, the nutrient release rate tends to be gentle. This phenomenon could be related with the gel strength of hydrogel network. With the decrease of gel strength, the nutrient release rate gradually increased. Figure 11b shows the release kinetics of SC-g-PAA/PAM/ Urea in water. As can be seen from Table 5, the n value in the release model was 1.3214, indicating the Case II release, erosion mechanism for the skeleton. In addition, the curve has a high goodness of fit, indicating that the Ritger-Peppas release model was applicable to explain the diffusional process [8,30,31]. The release mechanism was characterized by slow release in the early stage, fast release in the middle stage and slow release in the late stag, which was in line with the growth requirements of the crop.

Conclusions
Through the method of grafting copolymerization, a novel slow-release hydrogel fertilizer based on sawdust cellulose was successfully prepared. The AA, AM and sawdust cellulose participated in the formation of hydrogel networks in this process, significantly improved the mechanical strength of the hydrogel networks. The effect of reaction variables on the swelling behavior was analyzed. The reaction conditions were optimized to obtain the maximum water absorbency of 210 g/g in deionized water. In addition, the influences of salt solutions, ionic strength and solution pH on the swelling of the SC-g-PAA/PAM/Urea were investigated. SC-g-PAA/ PAM/Urea can absorb more water in the pH range 7-10. Compared to other salt solutions, SC-g-PAA/PAM/Urea was able to absorb more water in NaCl solution. The release behavior of fertilizer was analyzed using the Ritger-Peppas release model. The addition of SC-g-PAA/ PAM/Urea into soil could improve the water-retaining ability and reduce nutrient release ability. Therefore, the fertilizer has broad application prospects in agricultural production.