Biochar Grafted on CMC-Terpolymer by Green Microwave Route for Sustainable Agriculture

The deficiency of water sources and the environmental disposal of large amounts of biomass waste (orange peels) produces economic and environmental problems, though its conversion into biochar by a pyrolysis procedure might be used to improve soil productivity. In the current study, we investigated the performance of superabsorbent biochar composite grafted on CMC as a low-cost, alternative, and biodegradable terpolymer composite (IPNCB) for soil water retention capacity. The IPNCB composite was synthesized by both microwave and conventional routes. The optimal reaction parameters proved that the microwave route has a high grafting percentage (%G) and short reaction time compared to the conventional route. The superabsorbent composite was characterized using different methods: FTIR, TGA, and SEM. The results show that the equilibrium water swelling (EW) of the IPNCB composite was improved at a 2% biochar concentration. The incorporation of biochar (BC) into the polymer network improved the water holding capacity (WHC) to 57.6% and water retention (WR) to 9.1% after 30 days. The degradation test indicates the IPNCB composite has a good degradability rate. Mixing soil with the prepared IPNCB composite can improve plant growth and reduce water consumption through the irrigation of arid lands. The IPNCB composite is a candidate in sustainable agriculture applications.


Introduction
Water scarcity is a serious problem in various regions around the world, especially due to climate change. Water is the main factor for crop production and cultured zones [1]. The development of agriculture depends on solving these problems, and a potential method is using materials with high water absorption called superabsorbent hydrogels.
Superabsorbent hydrogels (SAPs), which can be used as water management resources for agricultural development, have recently attracted attention for their increased water holding capacity, decreased irrigation rate, and ability to enhance growth of plants and save water consumption [2]. These materials consist of three-dimensional networks and are mainly divided into chemical and physical crosslinking according to the material used. Chemical crosslinking can form hydrogels rapidly under mild condition with addition of crosslinker. Physically crosslinked hydrogels have electrostatic interaction, hydrogen bonds, hydrophobic interaction, and van der Waals force between the polymers without the addition of ionic crosslinking agents.

Biochar Production
Orange peel waste was collected, dried at 70 • C, and pyrolyzed in an oven under N2 at 350 • C for 3 h [26]. The produced biochar was ground, washed with 0.1 M HCl for 5 h, washed with distilled water to remove any impurities, and then dried in an oven at 70 • C for 24 h. Table 1 shows the estimated elemental composition of biochar.

Sandy Soil
The sandy soil sample was collected from the El-Hamoul area (31-07 N Latitude, 30-57 E Longitude, with an elevation of about 6 m above mean sea level), Kafr El-Sheikh Governorate, Egypt. Physical and chemical properties of the studied soil samples, which were determined using the appropriate methods as described by Kim et al. [27], are presented in Table 2.

Preparation of CMC-g-(TerPols)/BC by Conventional Method
The synthesis of CMC-g-TerPols superabsorbent hydrogel was achieved using a free radical polymerization technique. CMC is soluble in a specific quantity of d-water. At that point, two different weight ratios (1% and 2%) of biochar (BC) were added and sonicated for 20 min to form homogeneous dispersed solution. Added NaOH with a concentration 4 mol/L solution was utilized to neutralize the solution, and AA, Am, and AMPS were added consistently. When the temperature reached 70 • C, the amount of KPS in d-water was added to the mixture. After mixing for 15 min and decreasing the temperature to 40 • C, MBA in d-water was added to all the mixture with a purge of N2. The water bath Agriculture 2021, 11, 350 4 of 16 was kept at 70 • C to complete the polymerization reaction for 3 h [28] to get CMC-g-(TerPols)/biochar (IPNBC). This gel was cut into little pieces and washed by a suitable ratio of distilled water and ethanol to remove the unreacted monomers and other chemicals. The IPNBC was formed and dried overnight in an oven at 60 • C. The graft yield or percentage grafting (G) was calculated using Equation (1): where WO and W1 denote the weight of CMC and graft copolymer, respectively. The composition of CMC superabsorbent hydrogels is illustrated in Table 3.

Preparation of CMC-g-(TerPols)/BC by Microwave Method
CMC is soluble in a specific quantity of d-water. At that point, two different weight ratios (1% and 2%) of biochar (BC) were added and sonicated for 20 min to form homogeneous dispersed solution. NaOH with a concentration 4 mol/L solution was utilized to neutralize the solution, and AA, Am, and AMPS were added consistently. Then KPS and MBA in d-water were added to the mixture with a purge of N2. The solution was kept in the microwave reactor at 800 W, and the temperature was set to 70 • C for diverse timing. After the completion of reaction time the gel obtained was cut into little pieces and washed using a suitable ratio of distilled water and ethanol to remove the unreacted monomers and other chemicals. The IPNBC was formed and dried overnight in an oven at 60 • C. The graft yield or (%) grafting was calculated using Equation (1).

Swelling Behavior in Different Media and Equilibrium Water Absorbance of (CMC-TerPols)/BC Superabsorbent Composite
The equilibrium water absorbance and swelling of synthesized hydrogel were measured by immersing 0.5 g of dried IPNBC composite in d-water (200 mL) to reach swelling equilibrium state (Qeq) [29]. The swollen gel was filtered from the solution and dried. The swollen gel was then weighed, and the Equilibrium water absorbance was calculated with Equation (2): where Qeq is the equilibrium water absorbance (g/g) (EW) at time t (min), Ws is swollen hydrogel (g), and Wd is dried hydrogel (g). Swelling behavior of the CMC-g-(TerPols) superabsorbent in saline water (s-water) 0.9 wt% NaCl solution and several buffer mediums was measured as follows: 0.5 g of the superabsorbent was placed in 500 mL beakers into which 100 mL of saline or buffer solution was then poured. The swollen gels were then filtered, and the swelling behavior of IPNBC was calculated according to the above Equation (2).

Water Retention (WR) and Water Holding Capacity (WHC) of Soil with IPNCB Composite
The WHC% and WR% of soil with IPNCB are the main properties used to investigate the capacity of IPNBC composite to hold and retain the water inside its network matrix [30]. They were measured by taking 100 g of dry soil only (A), 100 g of dry soil mixed with 1.0 g of IPNCB (B), and 100 g of dry soil mixed with 2.0 g of IPNCB (C). Each sample was placed in a sealed tube with 200-mesh nylon fabric and weighed (WO). The (A), (B), and (C) samples were slowly soaked with d-water until saturation, and then the samples were weighed again (W1). The WHC % of the soil was calculated using Equation (3). The degradation rate of the IPNCB composite was determined by measuring the weight loss of the IPNCB composite with the incubation time in soil. The IPNCB composite (0.1 g) was stored in a nylon bag and then placed 5 cm under the surface of the soil and incubated for up to 30 days. The bags of IPNCB were then picked out at various times (5,10,15,20,25, and 30 days), washed and dried until constant weight, and then the IPNCB composite was weighed to calculate the weight loss with Equation (5).
where Wo and Wi are the weights of the IPNCB before and after degradation (g), respectively.

Characterization of IPNBC Superabsorbent Composite
The chemical structures were confirmed using Fourier transform infrared spectroscopy (ATI Matson Genesis Series FTIR™). The thermal properties of the prepared hydrogels were measured by using samples that were thermogravimetrically analyzed using a TGA 55 (Meslo, Sante Fe Springs, CA, USA). Film samples were placed in a pan of platinum and heated in the range of 300 to 800 • C under N2 atmosphere at a heating rate of 10 • C per minute, and weight loss was plotted versus temperature.
The morphology of the gel (freeze-dried for 24 h) was observed by using scanning electron microscopy (SEM). The surface images of hydrogels were recorded using a Quanta FEG 250 scanning electron microscope (FEI Company, Hillsboro, OR, USA) available from EDRC, DRC, and Cairo. Samples were mounted onto SEM stubs. Applied SEM conditions were a 10.1 mm working distance, with an in-lens detector with an excitation voltage of 20 kV. Figure 1 verifies the predicted mechanism of graft polymerization. The crosslinking procedure of AA, AMPS, and Am onto CMC chains was achieved both by conventional and microwave methods. This was carried out by using APS as a radical initiator and MBA as a crosslinking agent. APS was decomposed by heating to give sulfate radicals, which pull hydrogen atoms from the -OH groups of the CMC matrix to create macroradicals. AA, Am, and AMPS monomers can be grafted onto these active macroradicals and MBA in this stage to crosslink monomers with radicals on the CMC matrix to form a three-dimensional interpenetrating network-IPN structure. Through the formation of a 3D IPN network, BC was dispersed and bounded in a superabsorbent interpenetrating network.

Synthesis of CMC-g-(TerPols)/BC Composite and Spectral Analysis
The grafting and BC incorporation into the superabsorbent IPN were confirmed by comparing the FTIR spectra of CMC, BC, and IPNBC composite.
The FTIR spectra Figure 2a-c of the CMC-g-(TerPolys)/BC superabsorbent composite were compared. As shown in Figure 2a, of the biochar spectrum, the absorption bands at 805 and 915 cm −1 are related to the aromatic C-H out-of-plane bending vibration, the band at 1701 cm −1 is assigned to the C=O group, and the band at 1066 cm −1 is assigned to stretching C-N and C-O. The grafting and BC incorporation into the superabsorbent IPN were confirmed by comparing the FTIR spectra of CMC, BC, and IPNBC composite.
The FTIR spectra Figure 2a-c of the CMC-g-(TerPolys)/BC superabsorbent composite were compared. As shown in Figure 2a, of the biochar spectrum, the absorption bands at 805 and 915 cm −1 are related to the aromatic C-H out-of-plane bending vibration, the band at 1701 cm −1 is assigned to the C=O group, and the band at 1066 cm −1 is assigned to stretching C-N and C-O.
The shifting of the peak at 3437.7 cm −1 is attributed to -OH stretching of CMC, and the band of CMC at 1000-1166 cm −1 is reduced due to the contribution of -OH of CMC in reaction (Figure 2b,c).
The characteristic band at 1548, 1670, and 1040 cm −1 is due to carboxylate anions, carboxamide, and sulfonate groups, respectively. The introduction of COO-, -CONH, and -SO3 − was therefore helpful for the water absorbency of the composite because of their hydrophilic nature. Moreover, the presence of the hydrophilic functional groups and BC in the polymeric matrix were also beneficial to the water absorbency [31].

Optimization Time
Improving the optimization of the time of the reaction is crucial to improving graft yield (G%). The optimized time for the conventional method was 70 min, while in microwave synthesis, it was nearly 12 min. The graft yield (G%) of the two techniques is 7.8, which was reached at the termination stage. Any increase in the reaction time decreased The shifting of the peak at 3437.7 cm −1 is attributed to -OH stretching of CMC, and the band of CMC at 1000-1166 cm −1 is reduced due to the contribution of -OH of CMC in reaction (Figure 2b,c).
The characteristic band at 1548, 1670, and 1040 cm −1 is due to carboxylate anions, carboxamide, and sulfonate groups, respectively. The introduction of COO-, -CONH, and -SO 3 − was therefore helpful for the water absorbency of the composite because of their hydrophilic nature. Moreover, the presence of the hydrophilic functional groups and BC in the polymeric matrix were also beneficial to the water absorbency [31].

Optimization Time
Improving the optimization of the time of the reaction is crucial to improving graft yield (G%). The optimized time for the conventional method was 70 min, while in microwave synthesis, it was nearly 12 min. The graft yield (G%) of the two techniques is 7.8, which was reached at the termination stage. Any increase in the reaction time decreased the G% due to the reduction of active groups and predictable homopolymer creation [32]. The microwave method is therefore faster and more promising when compared to the conventional method, and the improved G% was achieved with minimal reaction time (12 min). The swelling behavior was also improved.
Our aim was to prepare a green superabsorbent composite with a 12 min reaction time and high swelling. WHC and WR performance was considered suitable for other studies. We studied the different optimization parameters (initiator, monomer, and crosslinker concentration) that affect graft yield using the microwave technique. Figure 3 shows the optimization ratio of initiator required to reach the high %G of IPNBC composite using the microwave technique. The maximum and optimal ratio of initiator was 0.7 g. Any excess of initiator concentration is damaged graft yield (G%); this may be due to the creation of many free radicals and homopolymers, which leads to smaller chains of the polymer matrix [33]. The findings outlined in Figure 4 show that 3 g of monomer reached the optimum %G, increasing grafting values continuously, and then decreased along with the monomer concentration mentioned above, so the %G decreased. This may be because any increase of monomer leads to the creation of homopolymers and a reduction of active sites on the CMC matrix through polymerization, which decreases graft yield (%G) [34].

Optimum Crosslinker Ratio
The effect of crosslinker ratio on the swelling performance was studied by taking 0.3 g of the IPNBC composite produced with different ratios of crosslinker (0.02-0.5 g), which was added to small beakers with distilled water. The samples were kept until swelling of the IPNCB composite, and the EW was calculated as given in Equation (2). From Table 4 it can be seen that the maximum swelling was recorded at 0.5 g of crosslinker ratio, then decreased with further addition. This may be attributed to Flory's theory; the swelling behavior of any polymeric matrix is related to the crosslinked density [35]. In radical polymerization, a high crosslinker ratio will provide many crosslinking sites and raise the crosslinked density. Therefore, the network space for holding water was lessened, i.e., the water absorbance capacity decreased [36].

Optimum Crosslinker Ratio
The effect of crosslinker ratio on the swelling performance was studied by taking 0.3 g of the IPNBC composite produced with different ratios of crosslinker (0.02-0.5 g), which was added to small beakers with distilled water. The samples were kept until swelling of the IPNCB composite, and the EW was calculated as given in Equation (2). From Table 4 it can be seen that the maximum swelling was recorded at 0.5 g of crosslinker ratio, then decreased with further addition. This may be attributed to Flory's theory; the swelling behavior of any polymeric matrix is related to the crosslinked density [35]. In radical polymerization, a high crosslinker ratio will provide many crosslinking sites and raise the crosslinked density. Therefore, the network space for holding water was lessened, i.e., the water absorbance capacity decreased [36].

Morphological Analysis SEM
Two of the most significant properties of superabsorbent hydrogels are porosity and pore size. SEM morphologies of the CMC-g-(TerPolys)/BC, and biochar (BC) are shown in Figure 5a,b, respectively. The BC in Figure 5a shows pores and high surface area that lead to a high number of adsorption sites over a short time, allowing much more water to be held in pores during irrigation [37]. Figure 5b shows that in IPNBC, the pore size is smaller and the compositive has a rough surface, which was due to the formation of crosslinked network, which was enhanced due to the diffusion of water into the IPN composite and increased swelling rate. These SEM results established that the BC was finely spread in the composite to form a homogeneous composition.
in Figure 5a,b, respectively. The BC in Figure 5a shows pores and high surface area that lead to a high number of adsorption sites over a short time, allowing much more water to be held in pores during irrigation [37]. Figure 5b shows that in IPNBC, the pore size is smaller and the compositive has a rough surface, which was due to the formation of crosslinked network, which was enhanced due to the diffusion of water into the IPN composite and increased swelling rate. These SEM results established that the BC was finely spread in the composite to form a homogeneous composition.

Thermogravimetric Analysis (TGA)
The effect of the grafting and crosslinking of monomer chains onto CMC and interpenetration of biochar within the CMC matrix on the thermal stability was studied. The thermal stability of the CMC, BC, and IPNBC were evaluated by comparing the weight loss (%) in the temperature range of 100 to 600 °C as shown in Figure 6. A three-stage decomposition mechanism was found, and maximum weight loss was observed after the first stage decomposition of crosslinked samples, indicating the chemical modification of CMC. In all cases initial decomposition temperature (IDT) was 100-200 °C, which is due to the loss of moisture or volatile compounds. The second stage was observed in the temperature range of 300 to 500 °C due to the elimination of side chains. Finally, third-stage decomposition was observed at 600 °C due to the breakdown of the crosslinked structure. In comparison, the rate of decomposition was lower in the case of IPNBC than CMC or CB, which indicates the more condensed and stable crosslinked polymeric network in IPNBC. This may be due to the incorporation of biochar into the polymeric network, which provides a protective barrier to both mass and energy transport in the hydrogel composite interpenetrating network.
An increase in hydrothermal severity leads to the generation of hydrochar with higher condensed carbon through the removal of H and O in a coalification-like process. The components of raw biomass go through various degradation processes. The major

Thermogravimetric Analysis (TGA)
The effect of the grafting and crosslinking of monomer chains onto CMC and interpenetration of biochar within the CMC matrix on the thermal stability was studied. The thermal stability of the CMC, BC, and IPNBC were evaluated by comparing the weight loss (%) in the temperature range of 100 to 600 • C as shown in Figure 6. A three-stage decomposition mechanism was found, and maximum weight loss was observed after the first stage decomposition of crosslinked samples, indicating the chemical modification of CMC. In all cases initial decomposition temperature (IDT) was 100-200 • C, which is due to the loss of moisture or volatile compounds. The second stage was observed in the temperature range of 300 to 500 • C due to the elimination of side chains. Finally, third-stage decomposition was observed at 600 • C due to the breakdown of the crosslinked structure. In comparison, the rate of decomposition was lower in the case of IPNBC than CMC or CB, which indicates the more condensed and stable crosslinked polymeric network in IPNBC. This may be due to the incorporation of biochar into the polymeric network, which provides a protective barrier to both mass and energy transport in the hydrogel composite interpenetrating network.

Equilibrium Water Absorbency and Swelling Behavior of IPNCB Composite in Different Media
The incorporation of BC into polymer matrix affects EW. The highest equilibrium water swelling, EW value was found to be at the weight ratio of 2% BC. It is clear that in Table 5, maximum equilibrium swelling is about 1900 g/g with microwave synthesis. This may be due to the presence of hydrophilic groups in the matrix structure and the porous property of biochar with high surface area, which enhances and increases water absorb- An increase in hydrothermal severity leads to the generation of hydrochar with higher condensed carbon through the removal of H and O in a coalification-like process. The components of raw biomass go through various degradation processes. The major components of waste biomass were highlighted for a better understanding of the underlying reactions and the interactions of the components in real biomass conversion during the degradation process [38,39].

Equilibrium Water Absorbency and Swelling Behavior of IPNCB Composite in Different Media
The incorporation of BC into polymer matrix affects EW. The highest equilibrium water swelling, EW value was found to be at the weight ratio of 2% BC. It is clear that in Table 5, maximum equilibrium swelling is about 1900 g/g with microwave synthesis. This may be due to the presence of hydrophilic groups in the matrix structure and the porous property of biochar with high surface area, which enhances and increases water absorbance capacity, and retention of water in the 3D interpenetrating network. On the contrary, when the concentration of BC increases, the water absorbance capacity decreases, which may be due to the superiority of the hydrophobic properties over the hydrophilicity of the IPNCB composite with an increase in biochar [40].
The water absorbance of IPNBC composite in s-water 0.9 wt% NaCl solution, as can be seen in Figure 7, shows that the decrease in swelling behavior is relative to the values in d-water. This action is attributed to a charge screening effect of ionic hydrogels [41], producing an imperfect anion-anion repulsion, led to a reduced ionic pressure between the SAP hydrogels and the water molecules, thereby decreasing water absorption capacity. D-water displays good results, as it has lower ionic concentration, which aids in better water intake by osmotic pressure.  Figure 8 shows the equilibrium swelling (EW) of IPNBC composite at different pH values. The IPNBC composite displayed a low EW in acidic media and maximum value in neutral medium. This phenomenon refers to the increase in pH value; carboxyl groups in the CMC are converted to carboxylate ions, which leads to repulsion and forms space between chains, allowing water particles to enter the IPNBC composite and enhancing water absorption [42]. However, as pH increases above pH 7, absorption capacity is reduced. This is possibly due to the existence of Na + cations in basic solutions, which avoid  Figure 8 shows the equilibrium swelling (EW) of IPNBC composite at different pH values. The IPNBC composite displayed a low EW in acidic media and maximum value in neutral medium. This phenomenon refers to the increase in pH value; carboxyl groups in the CMC are converted to carboxylate ions, which leads to repulsion and forms space between chains, allowing water particles to enter the IPNBC composite and enhancing water absorption [42]. However, as pH increases above pH 7, absorption capacity is reduced. This is possibly due to the existence of Na + cations in basic solutions, which avoid anion-anion repulsion and decrease space between chains, thereby decreasing water absorption capacity [42,43]. Table 6 summarizes the values of EW in different media.  Figure 8 shows the equilibrium swelling (EW) of IPNBC composite at different pH values. The IPNBC composite displayed a low EW in acidic media and maximum value in neutral medium. This phenomenon refers to the increase in pH value; carboxyl groups in the CMC are converted to carboxylate ions, which leads to repulsion and forms space between chains, allowing water particles to enter the IPNBC composite and enhancing water absorption [42]. However, as pH increases above pH 7, absorption capacity is reduced. This is possibly due to the existence of Na + cations in basic solutions, which avoid anion-anion repulsion and decrease space between chains, thereby decreasing water absorption capacity [42,43]. Table 6 summarizes the values of EW in different media.  Table 6. Swelling behavior of CMC-g-(TerPolys)/CB in various buffer media.

CB (%) EW (g/g)
D-water 2 1900 S-water 2 1600 Acidic 2 1190 Neutral 2 1455 Alkaline 2 1260 3.6. Physical Properties of the Soil with IPNCB Composite 3.6.1. Water Holding Capacity (WHC) The WHC% and WR% of soil with various amounts of the IPNCB composite (1% and 2%) are represented in Figures 9 and 10, respectively. The WHC% of soil without composite (0%) was 26%, whereas the WHC% of the treated soil was 41.8% and 57.6% for IPNCB of 1% and 2% (Figure 9). It can be clearly seen that CMC-g-(TerPolys)/BC had an outstanding result on the WHC% of soil, which enhanced with increasing concentration ratio of the IPNCB composite. The higher swelling absorbance (EW) due to existing hydrophilic function groups in polymer composite CMC-g-(AA-Am-AMPS) and BC was proved by the FTIR spectrum [44]. The incorporation of BC in the IPNCB composite enhances water holding due to its highly porous structure, which was confirmed by SEM morphology [45]. The WHC% of soil was 57.6% and 41.8% for CMC-g-(TerPolys)/BC of 1% and 2%. The soil can hold and store a significant amount of water when mixed with a larger ratio of 2% IPNCB composite concentration. As a result, soil wetness is improved, and water consumption is decreased. the FTIR spectrum [44]. The incorporation of BC in the IPNCB composite enhances water holding due to its highly porous structure, which was confirmed by SEM morphology [45]. The WHC% of soil was 57.6% and 41.8% for CMC-g-(TerPolys)/BC of 1% and 2%. The soil can hold and store a significant amount of water when mixed with a larger ratio of 2% IPNCB composite concentration. As a result, soil wetness is improved, and water consumption is decreased.

Water Retention (WR)
As seen in Figure 10, the water retention of the soil without the IPNCB composite decreases, with all the irrigated water lost over 12 days, while the WR% of the soil mixed with (1% and 2%) of the IPNCB composite was depleted after 24 and 30 days. Therefore, the water retention rate of the soil was increased by adding 2% of the IPNCB composite. This action may be due to the IPNCB composite having many hydrophilic groups and the highly porous structure of BC, which enhances the soil's physical properties and increases water absorption. The prepared IPNCB composite (2%) enhances the WR% of the soil to 9.1% after 30 days. Soil mixed with the prepared IPNCB composite can accordingly improve plant growth and reduce water consumption through irrigation of arid lands. The IPNCB composite is therefore a candidate in agriculture applications.  Figure 11 shows that the degradation rate of the IPNCB composite in soil after 30 days was calculated to be 23%. Soil is a complex system, including bacteria and enzymes. When the IPNCB composite was buried in the soil, swelling commenced after irrigation of soil, which allowed the interaction of the IPNCB composite with soil containing bacteria and enzymes [46]. IPNCB then started to decompose into small pieces through the hy-

Water Retention (WR)
As seen in Figure 10, the water retention of the soil without the IPNCB composite decreases, with all the irrigated water lost over 12 days, while the WR% of the soil mixed with (1% and 2%) of the IPNCB composite was depleted after 24 and 30 days. Therefore, the water retention rate of the soil was increased by adding 2% of the IPNCB composite. This action may be due to the IPNCB composite having many hydrophilic groups and the highly porous structure of BC, which enhances the soil's physical properties and increases water absorption. The prepared IPNCB composite (2%) enhances the WR% of the soil to 9.1% after 30 days. Soil mixed with the prepared IPNCB composite can accordingly improve plant growth and reduce water consumption through irrigation of arid lands. The IPNCB composite is therefore a candidate in agriculture applications. Figure 11 shows that the degradation rate of the IPNCB composite in soil after 30 days was calculated to be 23%. Soil is a complex system, including bacteria and enzymes. When the IPNCB composite was buried in the soil, swelling commenced after irrigation of soil, which allowed the interaction of the IPNCB composite with soil containing bacteria and enzymes [46]. IPNCB then started to decompose into small pieces through the hydrolysis of ether bonds (-O-). Figure 11 shows that the degradation rate of the IPNCB composite in soil after 30 days was calculated to be 23%. Soil is a complex system, including bacteria and enzymes. When the IPNCB composite was buried in the soil, swelling commenced after irrigation of soil, which allowed the interaction of the IPNCB composite with soil containing bacteria and enzymes [46]. IPNCB then started to decompose into small pieces through the hydrolysis of ether bonds (-O-). The degradation of TerPolys (AA-co-Am-co-AMPS) and bonds in CMC structure [47] causes a decrease of crosslink density of the IPNCB composite, enabling breakdown of the composite with bacteria and enzymes in the soil. The degradation rate in the present work is in agreement with other studies that found comparable values for similar evaluation times [48], indicating that the IPNCB superabsorbent composite is degradable and could be applied in arid land and various agricultural applications.

DR (%)
Time (day) Figure 11. Degradation rate of IPNCB in the soil.
The degradation of TerPolys (AA-co-Am-co-AMPS) and bonds in CMC structure [47] causes a decrease of crosslink density of the IPNCB composite, enabling breakdown of the composite with bacteria and enzymes in the soil. The degradation rate in the present work is in agreement with other studies that found comparable values for similar evaluation times [48], indicating that the IPNCB superabsorbent composite is degradable and could be applied in arid land and various agricultural applications.

Effect of IPNCB Composite on Plant Growth
Further confirming the efficiency of the prepared IPNCB composite on plant growth, as shown in Figure 12, the wheat seedling height and strength of leaves were increased, and leaves were greener in the case of 2% IPNCB than for 1% and 0% IPNCB. It was evident that the addition of IPNCB composite to the soil helped plant growth more than without it. Germination rate was 90.12 ± 2.44% in 2% IPNCB as compared to 1% IPNCB (88.34 ± 2.44%) and 0% IPNCB (70.33 ± 2.44%). The plant height and root length were increased by addition of IPNCB composite, and all data are summarized in Table 7. This may be attributed to biochar (BC) incorporated into the IPN matrix, which provides nutrients for plants and assists wheat growth.

Effect of IPNCB Composite on Plant Growth
Further confirming the efficiency of the prepared IPNCB composite on plant growth, as shown in Figure 12, the wheat seedling height and strength of leaves were increased, and leaves were greener in the case of 2% IPNCB than for 1% and 0% IPNCB. It was evident that the addition of IPNCB composite to the soil helped plant growth more than without it. Germination rate was 90.12 ± 2.44% in 2% IPNCB as compared to 1% IPNCB (88.34 ± 2.44%) and 0% IPNCB (70.33 ± 2.44%). The plant height and root length were increased by addition of IPNCB composite, and all data are summarized in Table 7. This may be attributed to biochar (BC) incorporated into the IPN matrix, which provides nutrients for plants and assists wheat growth.

Conclusions
An innovative superabsorbent composite based on biochar grafted on CMC-terpolymers was fabricated (IPNCB) through conventional and microwave methods. The micro-

Conclusions
An innovative superabsorbent composite based on biochar grafted on CMC-terpolymers was fabricated (IPNCB) through conventional and microwave methods. The microwave route improved the time of the polymerization reaction and shows high swelling behavior when compared with the conventional technique with optimized monomer, crosslinker, and initiator concentration. The addition of the 2% CB to the polymer matrix results in an improvement in swelling behavior in different media. TGA showed better thermal stability of the IPNCB composite as compared to the blank CMC. The porous structure of the IPNCB shown by SEM proves the incorporation of biochar and CB into the polymer network. In addition, the mixing of the INPCB composite into the studied soil can improve the WHC% and WR% rate of the soil and wheat plant growth. IPNCB shows good degradation rate in the soil, which helps to decrease environmental contamination. The prepared IPNCB composite therefore shows promise in sustainable agriculture irrigation.