Conversion of Lignocellulosic Corn Agro-Waste into Cellulose Derivative and Its Potential Application as Pharmaceutical Excipient

: Lignocellulosic biomass is widely grown in many agricultural-based countries. These are typically incinerated or discarded in open spaces, which further may cause severe health and environmental problems. Hence, the proper utilization and conversion of different parts of lignocellulosic biomasses (e.g., corn wastes derived leave, cob, stalk, and husk) into value-added materials could be a promising way of protecting both health and environments. In addition, they have high-potential for myriads applications (e.g., pharmaceuticals, cosmetics, textiles, and so on). In this context, herein, we isolated holocellulose (a mixture of alpha α , beta β , and gamma γ cellulose) from corn waste, and then it was converted into carboxymethyl cellulose (CMC). Subsequently, the prepared CMC was evaluated successfully to be used as a pharmaceutical excipient. Di ﬀ erent characterization tools were employed for structural, morphological, and thermal properties of the extracted holocellulose and synthesized CMC. Results showed that the highest yield of CMC was obtained 187.5% along with the highest degree of substitution (DS i.e., 1.83) in a single stage (i.e., size reduction technique) with the lowest particle size of holocellulose (100 µ m). This happened due to the use of a single stage instead of multiple stages. Finally, extracted CMC was successfully used as a pharmaceutical excipient with promising results compared to commercially available pharmaceutical-grade CMC.


Introduction
Lignocellulosic biomass is the most abundant resource in nature with immense potential for numerous applications [1]. Among different lignocellulosic biomasses, agricultural waste-based biomass consists of cellulose (35-50%), hemicellulose (20-35%), and lignin (10-25%) [2]. Corn (Zea mays) is one of the abundant cereal crops that is cultivated extensively across the world, which produces huge lignocellulosic biomass. The world's total corn production was 985,889.6 (1000 MT) from 2012 to 2017. USA was the top country for producing corn in the period of 2012-2017 with the production capacity of 343,167.8 (1000 MT), followed by the China, Brazil, Argentina, and Ukraine which produced

Estimation of Fatty and Waxy Matters, Pectic Substances, and Lignin
The dried powder sample was immersed in n-hexane-ethanol mixture in the solid to liquor ratio of 2: 200 for 10 h. The suspension was then filtered and washed with the residue with the fresh n-hexane-ethanol mixture. After drying the residue, fatty and waxy matters were calculated using the following formula.
where y is the loss in weight and x is the initial weight of the sample. The dewaxed and defatted powder was then heated with an ammonium oxalate solution (0.5% w/v)) in a liquor ratio of 0.1:10 at 80 • C for 3 consecutive days in a heating mantle. The level of the solution kept constant by adding hot DI water simultaneously. Finally, the suspension was filtered and the residue was washed with DI water and dried at 105 • C for getting pectic matters percentages: % of pectic matters = y × 100 x . (2) The dewaxed and depectinized dried powder was then treated with 72% sulfuric acid with solid to acid ratio of 1:15 at ambient condition. The mixture was kept for 1.0 h and diluted by DI water up to 3% acid solution. Subsequently, the mixture was refluxed for 4.0 h and kept overnight. The mixture was filtered and washed thoroughly with hot DI water and the residue dried until reaching the constant weight at 105 • C. The residue was considered as lignin, and the powdered sample from the filtrate was the delignified sample [20].

Isolation of Holocellulose
Holocellulose was isolated with a slight modification of the previously reported method [20]. Briefly, a suitable amount of dewaxed and depectinized powder corn wastes were treated with a 0.7% NaClO 2 solution at pH 4, and at 90-95 • C for 90 min with a liquor ratio of 1:80 (w/v). After being washed with DI water, chlorite holocellulose was treated with a 0.2% Na 2 S 2 O 5 solution for 15 min. Subsequently, the holocellulose containing solution was again filtered and washed thoroughly with distilled water, and finally dried at 60 • C to get the holocellulose.

Estimation of α-Cellulose and Hemicellulose (β and γ-Celluloses)
The α-cellulose and hemicellulose amount were determined to measure the total quantity in corn wastes [20]. Briefly, 1.0 g of the dried chlorite holocellulose was treated with an 18% NaOH (w/v) solution for 2 h in the ratio of 1:100 (w/v). The mixture was then filtered and washed thoroughly with 2% acetic acid solution, followed by hot water. The residue was dried at 105 • C until reaching constant weight. The dried residue (i.e., α-cellulose) was deducted from the weight of the holocellulose to estimate the amount of hemicellulose.
An equal volume of filtrate and 3N H 2 SO 4 was mixed and placed in a water bath for several minutes at 90 • C to coagulate the β-cellulose. The mixture was kept for 12 h to settle the precipitate. Afterward, the precipitate was separated and dried at 105 • C to obtain β-cellulose. Finally, the γ-cellulose was estimated by deducting the amount of α-cellulose and β-cellulose from the initial weight of the holocellulose. Here, diluted acids were used to extract as well as estimate the components of holocellulose from the lignocellulosic wastes due to its economic and environmental feasibility [21].

Conversion of Holocellulose into Carboxymethyl Cellulose
The general schematic diagram and synthesis route of CMC from the holocellulose of corn wastes is depicted in Figure 1. The synthesis of CMC includes two consecutive steps namely, alkalization and etherification. During alkalization, holocellulose was suspended in ethanol, and 30% (w/v) NaOH was added slowly for half an hour with vigorous stirring at room temperature, and the stirring was continued for an hour. In the etherification step, MCA (120%) was added gently to the slurry before placing into the water bath at 50 • C and heated for 3.6 h with intermittent stirring. The synthesized CMC was filtered and washed with 70% (v/v) alcohol to minimize the unwanted leftover and dried at 65 • C.
The outline of the mechanism for preparing CMC from holocellulose of corn wastes followed by two consecutive steps including basification as well as etherification are documented in Figure 1. 2% acetic acid solution, followed by hot water. The residue was dried at 105 °C until reaching constant weight. The dried residue (i.e., α-cellulose) was deducted from the weight of the holocellulose to estimate the amount of hemicellulose. An equal volume of filtrate and 3N H2SO4 was mixed and placed in a water bath for several minutes at 90 °C to coagulate the β-cellulose. The mixture was kept for 12 h to settle the precipitate. Afterward, the precipitate was separated and dried at 105 °C to obtain β-cellulose. Finally, the γcellulose was estimated by deducting the amount of α-cellulose and β-cellulose from the initial weight of the holocellulose. Here, diluted acids were used to extract as well as estimate the components of holocellulose from the lignocellulosic wastes due to its economic and environmental feasibility [21].

Conversion of Holocellulose into Carboxymethyl Cellulose
The general schematic diagram and synthesis route of CMC from the holocellulose of corn wastes is depicted in Figure 1. The synthesis of CMC includes two consecutive steps namely, alkalization and etherification. During alkalization, holocellulose was suspended in ethanol, and 30% (w/v) NaOH was added slowly for half an hour with vigorous stirring at room temperature, and the stirring was continued for an hour. In the etherification step, MCA (120%) was added gently to the slurry before placing into the water bath at 50 °C and heated for 3.6 h with intermittent stirring. The synthesized CMC was filtered and washed with 70% (v/v) alcohol to minimize the unwanted leftover and dried at 65 °C.
The outline of the mechanism for preparing CMC from holocellulose of corn wastes followed by two consecutive steps including basification as well as etherification are documented in Figure 1.

Estimation of Yield (%) of CMC
The yield of CMC was calculated based on a dry weight basis, where the weight of dried CMC was divided by the weight of holocellulose: where y and x is the weight of moisture-free CMC (g) and holocellulose (g), respectively.

Determination of Degree of Substitution (DS)
Before the determination of DS, the prepared CMC was acidified by using the modified protocols as described elsewhere [22,23]. Briefly, 2 g of CMC powder was placed in 100 mL of a beaker, and 40 mL of 95% ethanol was added, followed by 10 min agitation. Then, 2.5 mL of nitric acid was added and the solution was boiled in a hotplate. Subsequently, after removing the solution from the hotplate, it was stirred for 15 min. The liquid solution was decanted by using a vacuum pump and washed with 80% ethanol for several times. Then, the residue was washed with a small quantity of methanol and filtered. To analyze the DS, 1.0 g of dried CMC was added to 100 mL of distilled water, and 12.50 mL of 1 N NaOH was added with agitation. After completely dissolving the mixture, it was then titrated by 1 N HCl in the presence indicator phenolphthalein. The DS of CMC was calculated by the utilization of the following equations [23]: where O = milli-equivalents of used HCl per gram of specimen; P = volume of NaOH; Q = concentration in the normality of NaOH; R = volume of consumed HCl; S = concentration in normality of HCl; T = specimen grams; 162 is the molecular weight of the anhydrous glucose unit and 58 is the net increment in the anhydrous glucose unit for every substituted carboxymethyl group.

Determination of Molecular Weight
CMC powder was dissolved in 0.8 M NaOH aqueous solution to measure the molecular weight by using an Ostwald viscometer. From the value of intrinsic viscosity, the molecular weight of the CMC was calculated by using the Mark-Houwink-Sakurada equation i.e., [η] = K × M × a [19]. Where K, a, [η], and M are the constant for solvent, polymer shape factor, intrinsic viscosity, and molecular weight of CMC, respectively.

Structural Morphological and Thermal Study
FTIR spectrum analysis of the extracted holocellulose and synthesized CMC were performed by Fourier transform infrared (FTIR) spectroscopy (Perkin-Elmer 240C, Waltham, MA 02451, USA) in between 400 and 4000 cm −1 . For surface morphology of the dried samples, they were sputter-coated with gold for 10 min and then analyzed by using a scanning electron microscope (SEM) (Model-S 3400 N, VP SEM, Hitachi, Japan) using 20 kV accelerating voltage. The thermogravimetric analyses (TGA) of the samples were carried out using a Shimadzu TGA-50 system (Kyoto 604-8511, Japan) under a nitrogen atmosphere. The heating rate was 20 • C/min, and the temperature range was 25 to 600 • C. The prepared CMC was dried in an oven at 105 • for 120 min. Following this, the dried CMC was cooled in a desiccator until the ambient temperature was reached, and the final weight was taken. The moisture content was determined by this following equation [23]: where y and x is the final and initial weight of CMC (g), respectively.

Flow Properties of CMC
Flow properties of CMC were measured by performing several tests such as bulk and tap densities, true density, porosity, angle of repose, Carr's index, and Hausner's ratio. Detailed descriptions of these tests are given below.

Bulk and Tap Densities
A suitable amount of CMC powder (g) was poured in a 100 mL calibrated graduate cylinder and placed in a bulk density apparatus (LOGAN TAP-2S, New Jersey 08873 USA). After lightly tapping the cylinder, the occupied volume V 0 was estimated. After, that the cylinder was tapped 500 times for measuring the tap density and calculated by using the following relationship, respectively [24][25][26]: Tap density (TD) = w V 500 , where w is the weight of CMC powder, V 0 is volume before tapping, and V 500 is the volume of CMC powder after 500 times tapping.

True Density
The true density of the CMC powder was calculated by using a calibrated Quantachrome pycnometer (Quantachrome Corporation, FL, USA). CMC powder was dried at ambient temperature overnight under reduced pressure before analysis. True density was estimated by using the following formula [25,26]: True where w is the weight of the CMC powder and v is true volume of the CMC powder.

Porosity
The porosity of the CMC powder was determined according to the following equation [25,26]: 2.11.6. Angle of Repose The angle of repose of the CMC powder was measured by using a funnel and a Petri dish. At first, the funnel was fixed with a funnel holder. For making a cone, the CMC powder was allowed to emanate freely through the funnel. The height and diameter of the cone were recorded by a measuring scale and determined by using the following formula [25,26]: where D is diameter of the cone and h is the height of the cone.

Carr's Index and Hausner's Ratio
The Carr's index (CI) [25] and the Hausner ratio (HR) [26] were estimated by using the value tap and bulk density:

Chemical Composition, DS, Yield, and Molecular Weight of CMC
The chemical composition of corn waste residue including holocellulose (i.e., α, β, and γcellulose), lignin, pectic matter, fatty and waxy matter were estimated, and their results are shown in Table 1. From Table, it can be observed that the α-cellulose contents (i.e., 41.2%) were dominant among all other constituents, followed by β-cellulose and γ-cellulose contents. The amount of lignin, fatty and waxy matter, and pectic matters were 19.4%, 2.6%, and 3.6%, respectively. However, all types of holocellulose (i.e., α, β, and γ-cellulose) were converted into CMC through carboxymethylation. The synthetic route and reaction mechanism of synthesizing CMC from holocellulose is depicted in Figure 1. Corn wastes were converted into CMC depending on different particle sizes. The values of DS, yield (wt%), and molecular weight of the obtained CMC are illustrated in Figures 2-4 respectively. From Figure 2, it can be seen that the DS of the prepared CMC was greatly dependent on the particle size of the starting material (holocellulose). Therefore, it shows a trade-off relationship with the particle size of the holocellulose i.e., the values of DS gradually increased with the decreasing size of the holocellulose. The highest DS value of 1.83 was obtained from the lowest particle size of 100 µm.
The highest yield (i.e., 182.55%) of CMC was found with the lowest particle size of holocellulose i.e., 100 µm, whereas the yield declined with increasing particle size of holocellulose ( Figure 3). One might postulate that we have reported a higher yield of CMC in this study. This was highly desirable as the anhydrous glucose unit (molecular weight 162 g/moL) substituted into the sodium carboxymethyl groups (molecular weight 80 g/moL) based on the DS value. Therefore, the higher yield was highly desirable. However, we did a theoretical calculation and compared the data with the experimental findings. We found that theoretical yield was slightly higher (i.e., 7.0-8.6%) for theoretical mass yield, which indicated that successful substitution of the hydroxyl groups occurred by the sodium carboxymethyl groups. This result shows the resemblance with the principle that the reduced particle generates a larger surface area, which increases the chance of collisions between reactants and holocellulose. Therefore, the yield of CMC was increased by decreasing the holocellulose particle sizes [27].
From Figure 4, it can be noticed that the molecular weight of the prepared CMCs was significantly increased with the increasing DS value. From Figure 2, it was mentioned that the DS value was increased with the decreasing of holocellulose particle size. Since the smaller holocellulose particle size has a greater surface area, the excessive amount of reactants can infiltrate into the holocellulose at a time. In addition, Wang et al. mentioned that the etherification process significantly relies on the availability of the activated hydroxyl groups of AGU as well as the approachability of reactants [28]. Thus, higher DS, as well as molecular weight, were obtained due to the increasing number of -OH groups substituted by the sodium carboxymethyl group. The highest molecular weight of 457,910 Da was obtained with DS value of 1.83, whereas the lowest molecular weight of 100,388 Da was yielded with DS value of 0.34, as depicted in Figure 4. The molecular weight of the AGU was 162 g/mol, and the net gain in the AGU for every substituted sodium carboxymethyl group was 80 g/mol. Likewise, the carboxymethyl group is weightier than the -OH group, hence, the molecular weight of the CMC increased [23].
fatty and waxy matter, and pectic matters were 19.4%, 2.6%, and 3.6%, respectively. However, all types of holocellulose (i.e., α, β, and γ-cellulose) were converted into CMC through carboxymethylation. The synthetic route and reaction mechanism of synthesizing CMC from holocellulose is depicted in Figure 1. Corn wastes were converted into CMC depending on different particle sizes. The values of DS, yield (wt%), and molecular weight of the obtained CMC are illustrated in Figures 2-4 respectively. From Figure 2, it can be seen that the DS of the prepared CMC was greatly dependent on the particle size of the starting material (holocellulose). Therefore, it shows a trade-off relationship with the particle size of the holocellulose i.e., the values of DS gradually increased with the decreasing size of the holocellulose. The highest DS value of 1.83 was obtained from the lowest particle size of 100 µm. The highest yield (i.e., 182.55%) of CMC was found with the lowest particle size of holocellulose i.e., 100 µm, whereas the yield declined with increasing particle size of holocellulose ( Figure 3). One might postulate that we have reported a higher yield of CMC in this study. This was highly desirable as the anhydrous glucose unit (molecular weight 162 g/mol) substituted into the sodium carboxymethyl groups (molecular weight 80 g/mol) based on the DS value. Therefore, the higher yield was highly desirable. However, we did a theoretical calculation and compared the data with the experimental findings. We found that theoretical yield was slightly higher (i.e., 7.0-8.6%) for theoretical mass yield, which indicated that successful substitution of the hydroxyl groups occurred by the sodium carboxymethyl groups. This result shows the resemblance with the principle that the reduced particle generates a larger surface area, which increases the chance of collisions between reactants and holocellulose. Therefore, the yield of CMC was increased by decreasing the holocellulose particle sizes [27].
From Figure 4, it can be noticed that the molecular weight of the prepared CMCs was significantly increased with the increasing DS value. From Figure 2, it was mentioned that the DS value was increased with the decreasing of holocellulose particle size. Since the smaller holocellulose particle size has a greater surface area, the excessive amount of reactants can infiltrate into the holocellulose at a time. In addition, Wang et al. mentioned that the etherification process significantly relies on the availability of the activated hydroxyl groups of AGU as well as the approachability of

Structural Characterization
Different characterization techniques were used to characterize the synthesized CMC and holocellulose extracted from corn waste. For example, FTIR spectroscopy was used to analyze the surface functional groups present in the extracted holocellulose and synthesized CMC ( Figure 5). From the FTIR spectra of the corn wastes powder and holocellulose, a distinct difference was noticed. Significant differences were observed in the wavenumber in between 1800 and 1000 cm −1 . Several peaks such as at wavenumber 1741 cm −1 (due to C=O stretching), 1637 cm −1 (due to carbonyl stretching conjugate with aromatic rings), and 1513 cm −1 (due aromatic C=C stretch) were not found in the extracted holocellulose [29]. Most specifically, peak at wavenumber 1250 cm −1 (due to C-O stretching vibration) was significantly reduced, and peak at wavenumber 1513 cm −1 (due to aromatic C=C stretch) was absent in the holocellulose. This phenomenon indicated that the lignin was removed during the extract process [30]. On the other hand, the wavenumbers at around 1423 and 1640 cm −1 were due to -CH2 bending and O-H bending vibration of the absorbed water, respectively [31].
From the spectra of CMC, a broad absorption band at 3436 cm −1 was found, which indicated the presence of -OH group, and a band at 2928 cm −1 was attributed to the C-H stretching vibration [10,32]. In addition, a new and strong wavenumber at 1620 cm −1 was found, which confirmed the stretching vibration of carboxyl groups (COO − ), and a peak at 1424 cm −1 assigned to the salts of carboxyl groups [22]. The peaks at around 1327 and 1116 cm −1 can be assigned to -OH bending vibration and -C-O-C stretching, respectively. A wavelength of 898 cm −1 was found, which was due to 1 and 4-β glycosides of cellulose [11].

Structural Characterization
Different characterization techniques were used to characterize the synthesized CMC and holocellulose extracted from corn waste. For example, FTIR spectroscopy was used to analyze the surface functional groups present in the extracted holocellulose and synthesized CMC ( Figure 5). From the FTIR spectra of the corn wastes powder and holocellulose, a distinct difference was noticed. Significant differences were observed in the wavenumber in between 1800 and 1000 cm −1 . Several peaks such as at wavenumber 1741 cm −1 (due to C=O stretching), 1637 cm −1 (due to carbonyl stretching conjugate with aromatic rings), and 1513 cm −1 (due aromatic C=C stretch) were not found in the extracted holocellulose [29]. Most specifically, peak at wavenumber 1250 cm −1 (due to C-O stretching vibration) was significantly reduced, and peak at wavenumber 1513 cm −1 (due to aromatic C=C stretch) was absent in the holocellulose. This phenomenon indicated that the lignin was removed during the extract process [30]. On the other hand, the wavenumbers at around 1423 and 1640 cm −1 were due to -CH 2 bending and O-H bending vibration of the absorbed water, respectively [31].
From the spectra of CMC, a broad absorption band at 3436 cm −1 was found, which indicated the presence of -OH group, and a band at 2928 cm −1 was attributed to the C-H stretching vibration [10,32]. In addition, a new and strong wavenumber at 1620 cm −1 was found, which confirmed the stretching vibration of carboxyl groups (COO − ), and a peak at 1424 cm −1 assigned to the salts of carboxyl groups [22]. The peaks at around 1327 and 1116 cm −1 can be assigned to -OH bending vibration and -C-O-C stretching, respectively. A wavelength of 898 cm −1 was found, which was due to 1 and 4-β glycosides of cellulose [11].
For the characterization of cellulose-based materials, SEM is one of the general techniques for imaging the microstructure and morphology of the materials. The morphologies of isolated holocellulose and synthesized CMC were also observed using an optical microscope, depicted in Figure 6. Ribbon shaped or rod-like morphology was found for the synthesized CMC, which is similar with the reported literature [33]. Furthermore, from Figure 6, it can also be observed that the surface morphology of extracted holocellulose is smoother with very low damage. In contrast, the morphology of the prepared CMC was more extended, rough, and collapsed [34]. In addition, the isolated holocellulose was further treated with sodium hydroxide during carboxymethylation, thus the ruptured surface was obtained from the synthesized CMC [35]. From Figure 6, it can be found that the size of the particles of holocellulose and CMC were in the range of 1.0-3.5 and 1.5-3.5 µm (approximately), respectively. Processes 2020, 8, x FOR PEER REVIEW 10 of 16 For the characterization of cellulose-based materials, SEM is one of the general techniques for imaging the microstructure and morphology of the materials. The morphologies of isolated holocellulose and synthesized CMC were also observed using an optical microscope, depicted in Figure 6. Ribbon shaped or rod-like morphology was found for the synthesized CMC, which is similar with the reported literature [33]. Furthermore, from Figure 6, it can also be observed that the surface morphology of extracted holocellulose is smoother with very low damage. In contrast, the morphology of the prepared CMC was more extended, rough, and collapsed [34]. In addition, the isolated holocellulose was further treated with sodium hydroxide during carboxymethylation, thus the ruptured surface was obtained from the synthesized CMC [35]. From Figure 6, it can be found that the size of the particles of holocellulose and CMC were in the range of 1.0-3.5 and 1.5-3.5 µm (approximately), respectively. XRD analysis is one of the prime methods of physical research. This technique was employed to investigate the degree of crystallinity before and after the carboxymethylation of cellulose [36]. XRD  For the characterization of cellulose-based materials, SEM is one of the general techniques for imaging the microstructure and morphology of the materials. The morphologies of isolated holocellulose and synthesized CMC were also observed using an optical microscope, depicted in Figure 6. Ribbon shaped or rod-like morphology was found for the synthesized CMC, which is similar with the reported literature [33]. Furthermore, from Figure 6, it can also be observed that the surface morphology of extracted holocellulose is smoother with very low damage. In contrast, the morphology of the prepared CMC was more extended, rough, and collapsed [34]. In addition, the isolated holocellulose was further treated with sodium hydroxide during carboxymethylation, thus the ruptured surface was obtained from the synthesized CMC [35]. From Figure 6, it can be found that the size of the particles of holocellulose and CMC were in the range of 1.0-3.5 and 1.5-3.5 µm (approximately), respectively. XRD analysis is one of the prime methods of physical research. This technique was employed to investigate the degree of crystallinity before and after the carboxymethylation of cellulose [36]. XRD XRD analysis is one of the prime methods of physical research. This technique was employed to investigate the degree of crystallinity before and after the carboxymethylation of cellulose [36]. XRD analysis of the samples is presented in the Figure 7. The obtained peaks of the samples were analogous to both crystalline and amorphous phases [37]. From the figure, it can be inferred that that holocellulose is more crystalline than CMC. More clearly, holocellulose gave five peaks at 2θ = 14.2 • , 22.1 • , 27.4 • , 31.6 • , and 45.4 • and the peaks were sharp, which indicated the presence of more crystalline phases on its core structure. On the other hand, in the CMC diffractogram, less number of peaks were found after carboxymethylation in comparison with the diffractogram of holocellulose in Figure 7. Therefore, the presence of more amorphous structures in the CMC compared to holocellulose can be seen since the characteristic peaks at 2θ = 14.2 • , 22.1 • , and 27.4 • became broader and intensity was reduced significantly. In addition, it can be observed that the typical peak at 2θ = 31.6 • for extracted holocellulose disappeared in CMC [9]. On the contrary, the peak at 2θ = 45.4 • reduced dramatically for CMC. This was due to the decrease in crystallinity in CMC as holocellulose was transformed from the crystalline to highly amorphous phase after carboxymethylation [38]. Furthermore, the peak at 2θ = 14.2 • still appeared in CMC, which indicated the presence of some sort of crystallinity, although the peak intensity was not sharp enough as holocellulose. Even though the percentage of crystallinity of synthesized CMC was not quantitatively determined, it can be supposed that the CMC adopted a disordered arrangement as compared to isolated holocellulose. This characteristic can be attributed to the presence of the carboxymethyl moieties which substituted the hydrogen atoms of the hydroxyl groups of cellulose [39]. Finally, holocellulose was treated with the alkaline solution during the carboxymethylation process, and as a result they swelled and showed tension with neighboring crystallites of cellulose molecules [40]. crystalline phases on its core structure. On the other hand, in the CMC diffractogram, less number of peaks were found after carboxymethylation in comparison with the diffractogram of holocellulose in Figure 7. Therefore, the presence of more amorphous structures in the CMC compared to holocellulose can be seen since the characteristic peaks at 2θ = 14.2°, 22.1°, and 27.4° became broader and intensity was reduced significantly. In addition, it can be observed that the typical peak at 2θ = 31.6° for extracted holocellulose disappeared in CMC [9]. On the contrary, the peak at 2θ = 45.4° reduced dramatically for CMC. This was due to the decrease in crystallinity in CMC as holocellulose was transformed from the crystalline to highly amorphous phase after carboxymethylation [38]. Furthermore, the peak at 2θ = 14.2° still appeared in CMC, which indicated the presence of some sort of crystallinity, although the peak intensity was not sharp enough as holocellulose. Even though the percentage of crystallinity of synthesized CMC was not quantitatively determined, it can be supposed that the CMC adopted a disordered arrangement as compared to isolated holocellulose. This characteristic can be attributed to the presence of the carboxymethyl moieties which substituted the hydrogen atoms of the hydroxyl groups of cellulose [39]. Finally, holocellulose was treated with the alkaline solution during the carboxymethylation process, and as a result they swelled and showed tension with neighboring crystallites of cellulose molecules [40]. TGA is a technique by which the thermal stability of a material can be analyzed, where the material is decomposed by the heat, and bonds are broken within the molecule [41]. During the test, when the maximum degradation occurs at a certain temperate, it is considered as an indicator of the stability of the material. The TGA graph of holocellulose and CMC is shown in Figure 8. From the TGA is a technique by which the thermal stability of a material can be analyzed, where the material is decomposed by the heat, and bonds are broken within the molecule [41]. During the test, when the maximum degradation occurs at a certain temperate, it is considered as an indicator of the stability of the material. The TGA graph of holocellulose and CMC is shown in Figure 8. From the figure, the weight loss of moisture, volatile compounds, and carbohydrate polymers during the carbonization phase can be observed.
According to the figure, 2.3% weight loss was observed in the case of holocellulose. This was due to evaporation of absorbed water. Lin et al. [42] reported that the decomposition temperatures of hemicellulose and cellulose were in the ranges of 200-315 • C and 360-400 • C, respectively. In our case, we observed the degradation stage of hemicellulose and cellulose in the ranges of~300 • C and 380-400 • C, respectively. The weight loss of holocellulose was around 79% in the temperature range of 340 to 387 • C, but holocellulose started to degrade at around 300 • C, which was due to the thermal decomposition of glycoside linkages of cellulose (i.e., hemicellulose). In addition, the final change was observed after 380 • C, which was due to the decomposition of α-cellulose [43,44].
This unit was quite tough to break down at the referred temperature. Therefore, we assume that CMC should have higher stability than holocellulose (mass basis). This was mainly due to the presence of sodium ions in the residual mass, the degradation is quite tough. Henceforth, the mass residual mass (in the form of char) was expected to increase significantly, together with higher degradation temperature [46,47]. Therefore, in our case, we found that around 42.2% residual mass was even at a higher temperature compared to the holocellulose residual mass (i.e., ~21%).  On the other hand, CMC contained about 11.0% moisture. This primarily indicates that the CMC was more hygroscopic, and this is basically due to the presence of the carboxyl groups. The main decomposition of synthesized CMC was initiated at above 100 • C. This was due to the release of moisture from the CMC by the breaking of the hydrogen bond. Subsequently, the second and third stages decomposition was held between 283 and 318 • C. Finally, the weight loss was about 40%, which was probably due to the depolymerization of CMC by forming H 2 O, CO, CO 2 , and CH 4 [45]. In the temperature of 283 and 318 • C, CMC was decarboxylated as it contained COO − groups in their structure. In addition, as shown in Figure 8, the thermal decomposition temperature further occurred from about 318 to 377 • C, which indicated a further loss of the mass up to 42.2%. The rate of weight loss gradually enhanced with the increase in temperature. This indicated the presence of more non-volatile fraction in CMC. More clearly, from the previous discussion, we confirmed that CMC had more irregular fractions of the amorphous structure, together with the sodium carboxymethyl unit. This unit was quite tough to break down at the referred temperature. Therefore, we assume that CMC should have higher stability than holocellulose (mass basis). This was mainly due to the presence of sodium ions in the residual mass, the degradation is quite tough. Henceforth, the mass residual mass (in the form of char) was expected to increase significantly, together with higher degradation temperature [46,47]. Therefore, in our case, we found that around 42.2% residual mass was even at a higher temperature compared to the holocellulose residual mass (i.e.,~21%).

Feasibility as Pharmaceuticals Excipient
Generally, microcrystalline cellulose is being used as excipient, which is extracted from hardwood and also from purified cotton. This process is considered an expensive process. Therefore, investigations are going on to find out the cheaper resources like CMC [19]. In general, the excipient has no medicinal functions. Excipients are being utilized in many ways in the pharmaceutical industries. They can be used as a binder, disintegrator, coating material, diluent, lubricant, and so on [19]. Especially, during the manufacturing of tablets, physical parameters of the excipient plays a crucial role. Herein, we compared the physicochemical characteristics of synthesized CMC with commercial CMC (as excipient). The physicochemical characteristics of synthesized CMC powder and commercial CMC are shown in Table 2. Moisture content plays a crucial role in the case of flow properties of the powder. The effect of moisture on powder flowability depends on the amount of water and its distribution. It is quite common that the flowability of the powder often decreases with the increase of moisture content. Because a higher amount of water will increase the thickness of the adsorbed liquid layer, it increases the strength of liquid bridges. As a result, the powder becomes more cohesive and tends to form agglomerates [48]. It is clear from the table that the physicochemical properties of synthesized CMC power remained within acceptable limits with not more than 10% variations [49]. However, the bulk density rendered an estimate of the ability of a material to flow, which is related to compressibility. Each test was performed at least three times and average and standard deviation were considered. On the other hand, the tap density is a measure of the property of any sample of how well a powder can be packed in a confined space on recurring tapping. Bulk and tap density values of synthesized CMC showed almost similar behavior with the commercial CMC, as depicted in Table 2. It is generally considered that the better the potential for a material to flow and to re-arrange under compression, the higher the bulk and tapped densities [50]. In general, the higher true density of a powder reflects the better compressibility. The true density of synthesized CMC powder was approximately the same compared with commercial CMC. The total porosity or void fraction of a powder is the measurement of the void or empty space between the particles as well as pores within the particles of a material. In addition, it is a fraction of the volume of the void over the total volume, between 0-1 or as a percentage between 0-100%. The porosity value of the synthesized CMC was similar to the commercial CMC, which reveals the presence of poly-sized particles. Hence, synthesized CMC can easily be compressed during tablet making. The angle of repose of powder is another important criterion that gives a qualitative assessment of its internal and cohesive frictions. Angles of up to 40 • show reasonable flow potential of the solid powders. On the other hand, samples with angles greater than 50 • exhibit poor or absent flow [51]. In this study, the angle of repose of the synthesized CMC was found to be 38.5, which indicates there was no significant difference when compared with commercial CMC. To evaluate the flow properties of the powder, the Carr index and Hausner ratio have been commonly used. Carr's compressibility index exerts a clue of how much powder can be compressed, whereas Hausner index measures the cohesion between particles and the particle flows inversely with the values of the Carr index and Hausner ratio [50,52]. In the case of Carr's index, values ranged between 5 to 10, 12 to 16, 18 to 21, and 23 to 28, indicating excellent, good, fair and poor flow properties of the material, respectively [50]. The Carr's index of the synthesized CMC powder lies in the range of 5 to 10, which indicates its excellent flow properties. By contrast, the Hausner ratio (<1.20) often indicates good flowability of material, whereas a value of 1.5 or higher suggests a poor flow display by the material [52]. The Hausner ratio of the synthesized CMC showed a good flow property with value at around 1.3 in comparison with commercial CMC. Finally, it can be inferred from the discussion that the newly synthesized CMC from the agro waste can be a great source of commercial excipient.

Conclusions
CMC was successfully synthesized from extracted holocellulose. The highest yield of 182.55% was obtained with lower particle size (100 µm) of the holocellulose. The higher yield was reported due to the smaller particle sizes with DS of 1.83, which significantly contributed to incorporate more carboxylic groups in the CMC. Hence, it was used as a starting material for CMC synthesis. Different characterization analyses showed that CMC was successfully synthesized with ideal structural, morphological, as well as thermal properties. It was also found that the synthesized CMC had a good pharmaceutical excipient compatibility with a commercial excipient. The synthesized CMC with DS value of 1.83 can be a promising pharmaceutical excipient than other CMC bases excipients. Hence, this study has shown an efficient way of converting corn waste (lignocellulosic biomass) into value-added material, which can be a great aspect to be used as a pharmaceutical excipient, together with further applicability in real industrial application such as tablet making and other fields.