Investigation of the Effect of Process Parameters on Fabrication of Nanocrystalline Cellulose from Crotalaria Juncea

ABSTRACT Crotalaria juncea bast fibers a novel cellulose rich material is valorized by producing cellulose nanocrystals (CNCs) which gained much attention due to its unique properties. CNCs obtained during this study consisted of two steps: pretreatment of C. juncea fibers to obtain chemically purified cellulose followed by sulfuric acid hydrolysis. Efficacy of two different pretreatment methods chlor-alkali method (pre-treatment-I) and ultra sound assisted chlorine free alkaline peroxide (pre-treatment-II) methods was examined for CNC preparation. Pre-treatment-I was found to be more effective yielding higher crystallinity and higher surface sulfate ester groups containing CNCs compared to CNCs obtained using pre-treatment-II. Moreover the cellulose structure was altered with more pure cellulose-I structure obtained from pre-treatment-I. The process conditions of pre-treatment – I was optimized for CNC preparation. The acid concentration of 80%(w/v) was found to be optimized to produce CNCs with~43% yield, 80.9% crystallinity index having a rod-like structure (Length −120 ± 26 nm and diameter − 25 ± 5.5 nm). The surface charge density of the optimized CNC was found to be 0.34 meqv/g and a zeta potential −27.7 mV was recorded emphasizing stable dispersion.


Introduction
In recent years nanocellulose has gained much attention due to ever increasing environmental regulations and shift from petroleum-based products toward green environment-friendly materials (Dhali et al. 2021). Valorization of lignocellulosic biomass waste has been center of research for past decade as an alternative source of energy, but preparation of high-valued products such as nanocellulose from waste lignocellulosic biomass could open new avenues of sustainable circular economy by waste reutilization and minimization (Hafemann et al. 2019;Dhali et al. 2021). fragment due to high tensile strength, were valorized for efficient production of chemically purified cellulose. Furthermore, acid hydrolysis conditions for chlor-alkali pretreated samples were optimized for fabrication of CNCs. The CNCs obtained by various hydrolysis conditions were characterized for their physico-chemical structure using DLS-Zeta, FT-IR, XRD, SEM, TEM, TGA and also the surface charge was determined using conductometric titrations.

Materials
Crotalaria juncea of K12 variety was collected from ICAR-CRIJAF, Pratapgarh, UP, India, washed, dried and size reduced to 40 mesh size screen before pretreatment using Willey mill. The ground fiber was dried in hot air oven for 6 h at 70°C for removal of remaining moisture. Other chemical reagents such as sodium chlorite, acetic acid, sodium sulfite, sodium hydroxide, acetone, dimethylsulfoxide and sulfuric acid were procured from Merck India.

Preparation of CNC
Preparation of cellulose nanocrystals (CNCs) from lignocellulosic biomass mainly consists of two steps: a) Pre-treatment and b) Hydrolysis.

Pre-treatment-I
Pre-treatment-I consisted of four steps as elaborated by Mandal and Chakrabarty (2011). In a typical experiment, 1 g of the as prepared fiber was treated with 50 ml of 0.7% (w/v) sodium chlorite solution at its boiling temperature for 5 h at pH4, adjusted by 5% acetic acid and maintained with buffer solution of pH4, residue obtained was washed with distilled water and oven-dried at 40°C for overnight (PM-1).
PM-1 was then boiled with 250 ml of 5% (w/v) sodium sulfite solution for 5 h. Then the residue was washed with adequate distilled water for complete removal of lignin and partial removal of hemicellulose followed by drying (PM-2).
PM-2 was further treated with 250 ml of 17.5% (w/v) NaOH solution for 5 h at the boiling condition to remove hemicelluloses. The insoluble residue (cellulose) was collected by filtration and washed thoroughly until neutralization and air-dried (PM-3). PM-3 was further treated with 50 ml dimethyl sulfoxide (DMSO) at 80°C in an oil bath for 3 hours to increase the porosity into the cellulose rich substrate. The product thus obtained was then filtered, washed with distilled water and air-dried . The schematic of pre-treatment-I is presented in Figure 1a.

Pre-treatment-II
An alternate method was devised by us (Saha and Ghosh 2019) to pre-treat CJ to obtain CNC as represented in Figure 1b. In a typical experiment, 5 g of the milled C. juncea fiber was dispersed in 300 ml of distilled water using ultra-sonication (35 KHz Bio base Sonicator bath) at 50°C for about 30 min. The aqueous suspension was then filtered and residue was left for drying at hot air oven at 100°C for about 3 hours and then left under vacuum overnight. The dry residue was mixed with 200 ml 5 wt% NaOH. To the suspension 11 wt% H 2 O 2 was added drop-wise for about 5 minutes under continuous sonication. The experiment was carried out for 2 hours at 50°C. Then the residue was washed with distilled water and dried under hot air oven at 50°C for 6 hours followed by overnight vacuum drying (PM-5).

Acid-Hydrolysis
In the second step pre-treated dried residue (PM-4) was subjected to acid hydrolysis by heating with varying concentrations of sulfuric acid (fiber to liquor ratio of 1:20) at 50•C under strong agitation.
The hydrolysis was quenched by adding 5-fold excess water (100 ml) to the reaction mixture. The acid hydrolysis conditions of PM-4 were optimized by varying the acid concentration from 60% to 95% using 5 h till 80% and 1 h and 45 mins for 90% and 95% (w/v) respectively. The process conditions for different hydrolysis concentrations are summarized in Table 1.
The optimized sulfuric acid concentration of 80% (w/v) was employed to compare the efficacy of different pretreatment conditions. Consequently, both the pre-treated dried residues (PM-4 and PM-5) were subjected to acid hydrolysis by heating with 80% (w/v) sulfuric acid (fiber to liquor ratio of 1:20) for 1 h at 50•C under strong agitation yielding CNC-I and CNC-II.  The reaction mixture was cooled to room temperature and centrifuged for 10 min at 10,000 rpm. Supernatant was removed and the sediment was redispersed into distilled water and centrifuged for 3 to 4 times until it became turbid. To maintain exact ph 7 the turbid mixture was washed by distilled water using dialysis membrane. Then it was freeze dried (Labogene Coolsafe −110°C) to obtain powdered CNCs for further characterizations.

Yield determination
Yield of different pre-treated materials and CNCs after acid hydrolysis was determined gravimetrically based on chemically purified cellulose (PM-4) and raw material.

Structural and chemical characterizations
The structural variations of raw material, pre-treated materials and CNC were observed by FTIR spectroscopy using a JASCO FT/IR-4700 spectrophotometer. The FTIR spectrum of the samples was noted in the transmittance mode in the range of 4000-450 cm −1 .
X-ray diffraction data were collected using a Rigaku Miniflex X-ray diffractometer equipped with Cu Kα radiation at 30kV and 15 mA to investigate the XRD spectra of the cellulosic sample. Scattered radiation was detected in the range 2θ = 5-50°, at a speed of 3°/min. Crystallinity Index of all the samples was calculated using Equation 1 according to Segal's method (Segal et al. 1959) Scanning electron microscopy (SEM) photographs of raw material, pretreated material and CNC particles were captured using SEM JEOL JSM-6360 using a gold coating. A drop of dilute suspension of CNC was placed on a copper grid followed by drying it under table lamp followed by staining for 3 min with Ruthenium vapor. Transmission electron micrographs (TEM) photographs were taken using a TECNAIT12 FEI (Germany) transmission electron microscope with a voltage of 80 kV.
Particle Size was measured after equilibriating CNC suspension (0.1 wt. %) at room temperature for 1 hour, in a temperature regulated cell at 25°C, DLS/Zeta measurements were conducted by Malvern Zetasizer Nano-ZS instrument working at 173° scattering angle. Effective hydrodynamic diameters and size distributions were obtained using DLS.
Conductometric titration was used to quantify the sulfate half ester content CNC through the determination of surface charge density following the procedures of (Beck, Méthot, and Bouchard 2015) with some modification. A 150 mg of CNC sample was suspended into 50 ml of 0.001 M NaCl solution and stirred for 10 min and the resulting suspension was then titrated with 0.01 M NaOH solution. The sulfation value was then calculated using Equation 2 (Feng, Esker, and Roman 2010).
where μ=surface charge density (meqv/gm), C NaOH = Concentration of NaOH used for titration, V NaOH =Volume of NaOH required for Titration, C cnc =Concentration of CNC suspension, α cnc = amount of CNC suspension for titration.
Thermal stability of CNC was checked using Pyris Diamond TG/DTA, Perkin-Elmer, Singapore. Approximately 3 mg of each sample was heated from 30°C to 750°C at a heating rate of 15°C/min in a platinum crucible with alpha alumina powder as reference under N 2 flow of 150 ml/min.

Result and discussions
C. juncea is a cellulose rich energy crop containing only 7.04% lignin, 3.06% hemicellulose and rest 89.9% cellulose (Baksi et al. 2019) abundantly available in subtropical countries.

Yield of pre-treated materials and CNCs
Sodium sulfite employed in pre-treatment-I solubilized lignin-chlorine complex obtained during digestion with sodium chlorite. To certain extent hemicellulose was also removed through solubilization with sodium sulfite. Further treatment with NaOH, intermolecular ester bonds between lignin and hemicellulose were saponified facilitating removal of lignin and dissolution of hemicellulose. DMSO treatment helped to swell the cellulose enabling easy transport of hydrolyst (sulfuric acid) into the fibers in the subsequent acid hydrolysis step. Treatment of the chemically purified cellulose (CPC) substrate with sulfuric acid leads to esterification of hydroxyl groups while removal of the amorphous part takes place keeping the crystalline part intact. Grafting of negatively charged sulfate groups during acid hydrolysis leads to formation of stable dispersion in water due to electrostatic repulsion of electrical double layer. However, upon freeze drying, the crystalline cellulose became rod-like and aggregated to some extent due to the formation of hydrogen bonds resulting high surface energy of the CNC (Mandal and Chakrabarty 2011).
The yield of various pre-treated materials during pre-treatment-I is presented in Table 2a. The major changes in yield results were observed for RM to PM-1 and PM-2 to PM-3. This was expected as most of the lignin was removed during pre-treatment of RM with sodium chlorite solution in the first step while hemicelluloses were removed during treatment of PM-2 with NaOH. The weight loss was lower in case of PM-1 to PM-2 as remaining lignin and partial depolymerization of hemicellulose occurred during this step while the lowest weight loss of PM-3 to PM-4 attributed toward incorporation of porosity to the cellulose structure.
Yields of CNCs after acid hydrolysis with various sulfuric acid concentrations from chemically pure cellulose (PM-4) and raw material are tabulated and presented in Table 2b. With increase in acid concentrations, CNC yield increased (81% from PM-4 and 50.2 ± 0.18% from RM) till 70% (w/v) sulfuric acid concentrations while a decrease in yield was observed with further increase in acid concentrations. The initial increase in yield was due to efficient hydrolysis of chemically purified cellulose with increase in acid concentrations. The decrease in yield thereafter was probably due to the combined effect of lower reaction time and dissolution of more amorphous regions along with degradation of some crystalline cellulose structure at higher acid concentrations (Hafemann et al. 2019;Kusmono, Waziz Wildan, and Noer Ilman 2020). High CNC yield from C. juncea (~50% from raw material and 81% from purified cellulose) was obtained in the present study compared to 50% from purified corncob , 15.61% from Zea mays (Smyth et al. 2017), 55% from treated pineapple leaves (Marcos et al. 2013), 30% cassava bagasse (Pasquini et al. 2010), 46.4% from waste cotton (Wang et al. 2017) etc.

FT-IR analysis
Changes in the chemical structure of C. juncea during the course of pre-treatment-I and acid hydrolysis with varying sulfuric acid concentrations are depicted in Figures 2a and 2b respectively. Since major constituent of C. juncea is cellulose, the raw material exhibited almost all the characteristic groups of cellulose and thus very minute changes were observed during the course of pre-treatment. Broad peak around 3400 cm −1 assigned to -OH symmetric stretching, characteristic peaks of cellulose was present in all the spectra. A peak shift was observed from 2865 cm −1 for raw C. juncea attributed to -CH symmetrical stretching vibrations of polysaccharides to all the pre-treated materials and CNCs to 2966 cm −1 attributed to asymmetric -CH stretching of polysaccharides. The peak at 1720 cm −1 in the FTIR spectrum of ground C. juncea attributed to the C=O stretching vibration for the acetyl and uronic ester linkages in lignin, hemicellulose, pectin shifted to 1764 cm −1 after pretreatment with sodium chlorite (PM-1) due to formation of lignin chlorine complex and disappeared in the subsequent steps of pre-treatment indicating removal of lignin (Saha and Ghosh 2019). The spectral bands at 1514 cm −1 depict the aromatic ring present in lignin with C=C symmetrical stretching vibrations disappeared completely after first step of pre-treatment indicated efficient lignin removal in the very first step of pre-treatment-I. In addition, peak around 1660 cm −1 signifying O-H stretching of the absorbed water to cellulose become prominent with the course of pretreatment indicated increase in cellulose content with the advancement of pre-treatment. The peak at 1242 cm −1 present in the spectra of C. juncea ascribed to C-O stretching vibrations in aryl group of lignin tends to disappear after pre-treatment. While the bands at 1178 cm −1 and 1073 cm −1 were mainly due to asymmetric stretching vibrations of C-O-C bridge and also skeletal vibrations involving C-O stretching respectively assigned to polysaccharide structure became strong and prominent during the progression of pre-treatment. The band at 906 cm −1 ascribed to characteristic peak of glycosidic bond symmetric ring of polysaccharides became prominent with advancement of pre-treatment signifies increase in cellulose content and decrease in lignin (Hafemann et al. 2019). Peak around 670 cm −1 attributed to C-OH out of plane bending of cellulose became strong and prominent after pre-treatment.
There was no significant change in FTIR spectra observed between PM-4 and CNCs demonstrating main cellulose structure to be unaltered during acid hydrolysis as reported elsewhere (Shaheen and Emam 2017). Increase in acid concentrations did not show any significant alterations of cellulose backbone structure while exhibiting the characteristic peaks of cellulose (1370 cm −1 , 1335 cm −1 , 1162 cm −1 , 1070 cm −1 , 906 cm −1 , 677 cm −1 ). Nevertheless, with increase in acid concentrations the peak intensities at 906 cm −1 and 677 cm −1 increased till 80% w/v concentration. Minute changes in FTIR spectra were observed for CNC-90 and CNC-95 as peak shift from 906 cm −1 to 885 cm −1 occurred along with the appearance of a new satellite peak around 850 cm −1 . Also cellulose characteristic peak at 677 cm −1 got significantly reduced for CNC-90 and CNC-95 demonstrating initiation of cellulose degradation and or formation of cellulose-II structure.
The lateral order index (LOI) (1430 cm −1 /906 cm −1 ) and total crystallinity index (TCI) (1390 cm −1 / 2960 cm −1 ) were calculated according to Xu and Wang (Feng and Wang 2015) and were presented in Figure 2c. The total crystallinity index decreased significantly from RM to PM-1 while increased thereafter with the progression of pre-treatment and increase in acid concentrations during hydrolysis till 80% w/v exhibiting strong correlation with cellulose rich structure. Decrease in the same index with further increase in acid concentrations could be attributed to degradation of crystalline cellulose structure. On the contrary no strong correlation could be found for lateral order index with progression of pre-treatment or acid concentrations during hydrolysis. There was an initial increase in LOI from RM to PM-3 while a decrease in the same was observed for PM-4 and CNC-60. A further increase in the same index was observed with increase in acid concentrations till 80% (w/v) and decrease in the same with further increase in acid concentrations. Since 1430 cm −1 attributes contributions from all the constituents, an initial increase could probably due to abundance of hemicellulose and cellulose structure due to removal of lignin. LOI also showed similar trends as TCI with the increase in acid concentrations, initial increase till 80% (w/v) and decrease thereafter strengthening the hypothesis of degradation of crystalline structure of cellulose at higher acid concentration.

XRD analysis
Adjacent cellulose molecules are linked together by the interaction of hydrogen bonds and van der Waals forces ensuing crystalline structure of cellulose (Gabriel et al. 2021). Figure 3a shows the XRD patterns of all the pre-treated materials and CNCs obtained using various acid concentrations, all of which demonstrated peaks corresponding to crystalline cellulose structure. PM-1 and PM-2 exhibited cellulose-I structure with characteristic peaks around 2θ = 22.5, 14.8, 16.05, 35.5 corresponding to (2 0 0), (−1 1 0), (1 1 0) and (4 0 0) lattice planes respectively (Orrabalis et al. 2019;Yu et al., 2014). A change was observed from cellulose-I structure to cellulose-II for PM-2 to PM-3, PM-4 could be attributed to alkaline treatment of PM-2 by directly interacting with cellulose. PM-3, PM-4 exhibited three main characteristic peaks of cellulose-II structure at around 2θ = 12.01, 19.85 and 21.85 (Gabriel et al. 2021;Yu et al. 2014). Although there was a structural change in cellulose, the crystallinity index remained almost constant during the advancement of pre-treatment as depicted in Figure 3b. CNC-60, CNC-65, and CNC-70 also demonstrated similar cellulose-II structure as PM-3 and PM-4 but there was an increase in intensity after acid hydrolysis owing to dissolution of amorphous regions of cellulose which was further supported by the increase in crystallinity after acid hydrolysis as illustrated in Figure 3b. While increasing the acid concentrations from 60% to 70% (w/v) although no structural changes took place, intensities of all the peaks became diminished. This can directly be correlated to lower crystallite size with increase in acid concentrations while no significant change in crystallinity index was observed (Figure 3b). Further increase in acid concentrations not only altered the cellulose-II to cellulose-I structure but the peaks become narrower and intense (Yu et al., 2014) while the crystallinity index remained similar for CNC-80. Small decrease in crystallinity index was observed for CNC-90 while significant decrease in the same was observed for further increase in acid concentrations (CNC-95) confirming degradation in crystalline structure of cellulose. High crystallinity index for various acid concentrations (~81%) obtained during present study was higher or comparable with reported values for CNCs from different sources (

Morphological analysis
The morphology of the raw material, pre-treated materials (PM-3 and PM-4) and CNCs (CNC-60 and CNC-80) were recorded using SEM images whereas single cellulose nanocrystal rod like morphology was observed by TEM analysis. The RM showed smooth cylindrical structure as presented in Figure 4a while disintegrated fibrillar cellulosic structure was observed for PM-3 ( Figure 4b). The diameter of the original plant fiber was larger compared to the diameter of pre-treated materials. Moreover, they appear as a composite form of several microfibrils Figure 4a. The fiber surface of the raw material shown in the images found to be smooth due to the presence of waxes and oil. At first sodium chlorite was used for removal of lignin through depolymerization. On subsequent alkali treatments removes hemicellulose from the rest of fiber and make the cellulose water soluble. These processes destroy the composite form of microfibrils and result in micrograph in Figure 4b whereas the diameter of the fibrils was also reduced to a great extent, as the consequence of removal of non-cellulosic constituents from the fiber (Cherian et al. 2010). PM-4 showed fibrous structure with higher porosity induced by DMSO as illustrated in Figure 4c. CNC-60 exhibited disintegrated cylindrical structure (Figure 4d) while rod shaped structure was evident for CNC-80 (Figure 4e). Although the EDS spectra of CNC-60 did not show any sulfate group due to low degree of sulfation, CNC-80 exhibited sulfate group of approximately 0.32 which was a close approximation of the calculated degree of sulfation (0.34) for CNC-80 as discussed in next section. Single crystal TEM micrographs of CNC-60 and CNC-80 are compared in Figure 4f. It is evident from the figure that the diameter and length of CNCs decrease with increasing acid concentrations. The length and diameter of CNC-60 were 500 ± 34 nm and 80 ± 6 nm respectively while length and diameter of CNC-80 reduced to 120 ± 26 nm and 25 ± 5.5 nm respectively. From this figure it can also be concluded that due to presence of surface half ester groups, individual particles repel each other and with highly dilute dispersion it is possible to obtain single crystal micrograph.  Figure 5 represents changes in degree of sulfation with the variation in sulfuric acid concentrations. With increase in sulfuric acid concentration there was an increase in degree of sulfation from 0.04 ± 0.0032 meqv/g for CNC-60 to 0.43 ± 0.0083 meqv/g for CNC-90 while a decrease to 0.31 ± 0.0035 meqv/g was observed for CNC-95. This was due to the fact that increase in acid concentration increased available half-sulfate ester group to react to cellulose thus increasing the degree of sulfation. Decrease in the same could be attributed to the fact that some crystalline structure degraded at this very high sulfuric acid concentration resulting desulfation and drastic decrease in crystallinity of CNC.

Diffractive Light Scattering (DLS) and zeta potential
DLS experiment was carried out to obtain a rough estimate of hydrodynamic diameter of the cellulose nano materials, widely accepted technique for size determination.
The particle size analysis results depicted in Figure 6 illustrated initial decrease in hydrodynamic diameter with increase in acid concentrations till 80% (w/v) while an increase with further increase in acid concentrations could be attributed to incomplete reactions and degradation of cellulose nanocrystals. Initial decrease in diameter was due to dissolution of higher amount of amorphous regions leading to smaller sizes of cellulose nanocrystals.
The zeta potentials, the most important parameter for determination of the stability of CNC in aqueous media, of a series of samples prepared under various hydrolysis conditions (sulfuric acid percentage) were measured and presented in Figure 6. CNC-60, CNC-65, CNC-70 exhibited almost similar around −24 mV zeta potential although a decrease in trend was observed with increase in acid concentrations. The sample prepared using 80% sulfuric acid showed lower negative value (−27.7 mV)  and this was found to decrease further with increase in percentage of sulfuric acid. This was mainly due to the presence of a larger amount of negatively charged sulfate groups on the surface of the CNCs leading to repulsive forces and thus producing stable dispersions. The colloidal system becomes unstable between Zeta Potential values of+20 mV to −20 mV. It can be concluded from the above results that the CNCs fabricated by varying acid concentrations during this study produced stable dispersions in water owing to their small size and high half sulfate surface ester groups.

Thermogravimetric (TGA) analysis
TGA/DTG curves of Crotalaria juncea (RM), pure cellulose (PM-4) and the acid hydrolyzed nanocelluloses (CNC-80 and CNC-90) are shown in Figure 7. A single degradation peak around 380°C was observed for both RM and PM-4. High thermal stability of RM and PM-4 can be attributed to very high cellulose content (90%) of C. juncea fibers (Baksi et al. 2019) having highly crystalline structure (Hafemann et al. 2019). PM-4, more thermally stable compared to RM (degradation peak shifted from 380°C to 390°C), was due to removal lignin and hemicelluloses which has low decomposition temperature during alkaline pre-treatment of C. juncea. Owing to amorphous nature, hemicellulose containing acetyl group and lignin having complex aromatic ring structure are less thermally stable compared to cellulose (Kusmono, Waziz Wildan, and Noer Ilman 2020;K. Song et al. 2019). The initial weight losses started at ∼33°C for both untreated Crotalaria juncea (RM) and PM-4 while CNCs showed higher initial weight loss temperature (∼35°C). High solvation capacity with water molecule was responsible for higher weight loss temperature of CNCs (35°C). Water was evaporated near about 110°C for all samples. Higher weight loss around 100°C for CNCs compared to RM and PM-4 was attributed to moisture absorption by isolated CNCs. The highest weight loss for CNC-80 for this region attributed to higher moisture absorption (Gabriel et al. 2021;Kusmono, Waziz Wildan, and Noer Ilman 2020;K. Song et al. 2019;Hafemann et al. 2019) and less dehydration at lower acid concentration during hydrolysis. The degradation of raw Crotalaria juncea started at 310°C and the rate of degradation continued up to 400°C whereas PM-4 degradation began at 300°C and the rate of degradation was maximum at 370°C. The degradation of CNC-90 and CNC-80 took place around 260°C and 310°C leading to lower thermal stability because of their nano-sizes, greater number of free ends in the chain of CNCs, and presence of highly sulfated amorphous regions. In general, thermal degradation of pure cellulose involves some major steps including dehydration, depolymerization and decomposition of glycosyl followed by formation of residue. A second peak of weight loss around 600°C observed for CNC-90, was due to the formation of lower molecular weight gaseous products from charred residues (K. Song et al. 2019). Presence of sulfate groups lower the activation energy, resulting lower thermal stability of CNCs (Hafemann et al. 2019). Higher sulfate content in CNC-90 was responsible for lower thermal stability. In addition, formation of cellulose-II structure might also lowered the thermal stability of CNC-90 in comparison with CNC-80 as cellulose-II has lower degradation temperature than cellulose-I (Xing et al. 2018). This could also be the reason for higher weight loss for CNC-90 compared with that of CNC-80.

Comparison of pre-treatment-I and pre-treatment-II on preparation of CNCs
In this section CNCs obtained by acid hydrolysis using different pre-treatment methods have been compared to comprehend the efficacy of two different pre-treatment methods on the formation and properties of CNCs. Since previous results of pre-treatment-I revealed 80% (w/v) sulfuric acid concentration to be the optimum for preparation of CNC (CNC-I), this acid concentration was further employed for pre-treatment-II (CNC-II) for comparison purposes.
FTIR analysis of the prepared CNCs (CNC-I and CNC-II) revealed crystalline chemical structure of cellulose associated with these samples (Figure 8a). The peak at 3411 cm −1 signifies the presence of -OH group, as the peak is bulgy. The most prominent band in alcohols is due to the O-H bond, and it appeared as a strong, broad band covering the range of about 3000 -3700 cm −1 for both CNC-I and CNC-II. A carboxylic acid functional group combines the features of alcohols and ketones because it has both the O-H bond and the C=O bond. Therefore, carboxylic acids showed a very strong and broad band covering a wide range between 2800 and 3500 cm −1 for the O-H stretch. At the same time they also show the stake-shaped band in the middle of the spectrum around 1710 cm −1 corresponding to the C=O stretch which was absent for both CNC-I and CNC-II (Mandal and Chakrabarty 2011). But a peak around 1760 cm −1 was evident for CNC-II which can be ascribed to presence of carbonyl groups generated due to oxidation during pre-treatment-II with high amount of hydrogen peroxide, a strong oxidizing agent. While the bands at 1178 cm −1 and 1073 cm −1 were mainly due to antisymmetric stretching vibrations of C-O-C bridge and also skeletal vibrations involving C-O stretching which contributes to the cellulose backbone were observed for both CNC-I and CNC-II. The band at 906 cm −1 , the characteristic peak of glyosidic bonds present in the cellulose was evident in both CNC-I and CNC-II. But this characteristic peak was sharper in CNC-I compared to that of CNC-II confirming higher amount of ordered cellulose structure. Another cellulose characteristic peak around 677 cm −1 showed differences in shape for CNC-I and CNC-II was probably due to formation of cellulose-II structure for CNC-II as observed during XRD characterization.
XRD characterizations were performed to analyze the crystallinity of CNC extracted from Crotalaria juncea using conventional pre-treatment method (CNC-I) as well as that of CNC obtained after pre-treatment using sonication method (CNC-II). Structural differences were observed between CNC-I and CNC-II structure as evident from XRD data (Figure 8b). Cellulose-I structure was conformed for CNC-I while CNC-II exhibited presence of cellulose-II structure confirming the fact that not only acid concentrations during hydrolysis reaction but pre-treatment method also play an important role in formation of different cellulose structure. The acid hydrolysis treatment of CNC is expected to better dissolve amorphous zones under the specified conditions used in this study. This process shows hydronium ions can penetrate into amorphous regions of cellulose, promoting the hydrolytic cleavage of glycosidic bonds and the release of individual crystallites. The crystallinity index of CNC-I (80.9), higher than that of CNC-II (77.39) was due to transformation of cellulose-I to cellulose-II structure and also due to sharper diffraction peak at 2θ = 22.5°. These results are in accordance with FTIR findings.
CNC obtained by H 2 SO 4 hydrolysis often possesses a negatively charged surface, which help uniform dispersion in water due to electrostatic repulsion. The calculated value of degree of sulfation for CNC-I was found to be 0.34 meqv/g, which confirmed higher degree of sulfation compared to CNC-II (0.067 meqv/g). This was probably due to the difference in pre-treatment which directly affected the formation and structural differences in naocrystalline cellulose structure.
The physico-chemical properties of CNCs obtained in this study could effectively be used as a reinforcing agent for cement paste for building materials, nanocomposites, coating additives, hydrogel for controlled drug release, etc., as similar properties of CNCs obtained from various source materials are reported elsewhere (Molnes et al. 2018;Szyma 2019;Mendoza et al. 2021;Mekonnen, Haile, and Ly 2021;Sengupta and Debnath 2018;Zhang et al. 2019;Li et al. 2013;Yin et al. 2016) as depicted in Table 3.

Conclusions
C. juncea proved to be an excellent source for crystalline nanocellulose (CNC) preparation with yield as high as~43% from raw material having crystallinity index of~80.9. 80% H 2 SO 4 concentration proved to be the optimized acid concentration for this present study as highest yield of CNCs (~43%) with highest crystallinity index (~80.9) was observed for CNC-80. The FTIR results also revealed similar trend and highest LOI and TCI was observed for CNC-80 confirming higher crystallinity. Although highest degree of sulfation was observed for CNC-90, it was less thermally stable compared to CNC-80 as demonstrated by TGA analysis. The DLS-Zeta results confirmed lowest hydrodynamic diameter for CNC-80 having a zeta potential value of −27.7 mV confirming formation of stable dispersion in water. Conventional and ultrasound assisted pre-treatment was further compared for 80% acid hydrolysis condition and conventional pre-treatment proved to be more effective compared to that of ultrasound assisted pre-treatment. CNC-I (produced by conventional pretreatment) exhibited higher degree of sulfation and higher crystallinity compared to CNC-II (produced by ultrasound assisted pre-treatment). In the present study transformation of cellulose-I to cellulose-II structure was observed for conventional pre-treatment to ultrasound assisted pretreatment.
• Highest degree of sulfation was observed for CNC-90 but was less thermally stable compared to CNC-80.
• The DLS-Zeta results confirmed lowest hydrodynamic diameter for CNC-80 having a zeta potential value of −27.7Wang, ZhanhongmV confirming formation of stable dispersion in water. • Transformation of cellulose-I to cellulose-II structure was observed for conventional pre-treatment to ultrasound assisted pre-treatment

Disclosure statement
No potential conflict of interest was reported by the authors.