Studies on Mechanical, Thermal and Morphological Properties of Betel Nut Husk Nano Cellulose Reinforced Biodegradable Polymer Composites

: Nanocellulose has recently gained a signiﬁcant level of attention from academic and industrial researchers due to its non-toxic, biocompatible, bio-degradable, low-cost, and easy availability that connects many applications. In this research, cellulose extracted from betel nut husk ﬁber (BNHF) was converted to nanocellulose by chemical technique to examine their potential for use as reinforcement in bio-composite applications. The cellulose isolated from BNHF was subjected to acid hydrolysis using 62% sulfuric acid under ultrasonic treatment to convert cellulose into nanocellulose. The particle size of nanocellulose was determined by particle size analyzer. The morphology, structure and thermal properties of nanocellulose were also determined by scanning electron microscope (SEM) and Fourier-transform infrared (FTIR), thermogravimetric analysis (TGA), and di ﬀ erential scanning calorimetric (DSC) analysis. The bio-composites of nanocellulose–polyvinyl alcohol (PVA) and cellulose–PVA were prepared with di ﬀ erent weight percentages (1–5%) of nanocellulose and cellulose via casting methods. The tensile, thermal and morphological properties were characterized for all composites. Enhancement in the tensile, thermal, and morphological properties was found in the nanocellulose–PVA biocomposites. (wt%) up to 2% ﬁber for both cellulose and nanocellulose reinforced PVA composite then decreases. Nanocellulose reinforced PVA composite showed higher tensile strength than cellulose–PVA composite which indicate the good dispersion of nano ﬁber in PVA matrix and good interfacial adhesion between PVA and nanocellulose. Nanocellulose reinforcement in PVA composite enhanced the tensile strength of composites. 2% cellulose and nanocellulose reinforced PVA composite give the highest tensile strength. Elongation at break decreases when increasing the ﬁber loading of composite, but cellulose reinforced PVA composites showed higher elongation at break.


Introduction
Cellulose has attracted much attention from many researchers due its availability and excellent properties, including special morphology and geometrical dimensions, crystallinity, high specific surface area, rheological properties, liquid crystalline behavior, alignment and orientation, mechanical reinforcement, barrier properties, surface chemical reactivity, biocompatibility, biodegradability, lack of toxicity etc., especially in the form of nano-fibers [1]. Cellulose existing in natural fiber is one of the most abundant, renewable, and biodegradable polymer resources produced by nature on the earth. It has been used as a manufacturing material for several commodities in the food and pharmaceutical industries, as well as in paint, textiles etc. [2]. However, cellulose application in high value-added areas is still limited due to its hygroscopic nature and lack of melting properties. For the past few years, the preparation of cellulose nano-crystals (CNCs) and their application in nano composite materials have gained increasing attention because of their inherent properties like elastic modulus (130-150 GPa), high specific area (up to several hundreds of m 2 /g), high length to width ratio (up to several hundred) combined with low density (1.6 g/cm 2 ), low thermal expansion (0.1 ppm·K −1 ), biodegradability and renewability [3]. CNCs are mostly produced from various cellulosic materials,

Materials and Methods
Betel nut fruit husk fibers were used as reinforcing material in this research work. Betel nut is the fruit of Areca palm tree (Areca catechu). Matured betel nuts were collected from local betel nut plantation field, Barisal, Bangladesh. The BNHF is the fibrous part of the fruit. The analytical grade sodium hydroxide (Merck, Germany), sulfuric acid (Merck, India), polyvinyl alcohol (Mw approx. 60,000, Merck, Germany), 90% ethanol, purified benzene, glacial acetic acid, and reagent grade acetone were used in this study.

Analysis of the Constituent of Betel Nut Husk Fiber
The BNHF fibers were extracted from betel nut fruits manually by rejecting the hard portion of fruits. The fibers were washed with soap flake first and then with distilled water. Finally, the washed fibers were dried at 105 • C in an oven and stored. The chemical composition of BNHF samples in different processing stages were determined followed by Solvent Extractives of Wood and Pulp [TAPPI T204] standard method [14,15].

Estimation of Aqueous Extract
Dried fibers were heated with distilled water at 60 • C for 2 h and then the fibers were separated by filtration. Collected fibers were dried at 105 • C for constant weight. The calculated loss in weight gave the amount of aqueous extract in fiber.

Estimation of Fatty and Waxy Matters
Dried fibers were immersed in benzene-ethyl alcohol mixture (1 volume of ethanol and 2 volume of benzene) contained in a beaker in the ratio of 1 gm dried fiber per 100 mL of the mixture and then allowed to stand for 10 h then the fibers were washed several times with fresh benzene-ethyl alcohol mixture and finally with alcohol. Then, the fibers were dried at 105 • C for constant weight. The loss in weight on extraction with solvent mixture gives the amount of fatty and waxy matters present in betel nut fiber.

Estimation of Pectic Matters
The dried, de-waxed fibers were taken in a beaker and heated with 0.5% ammonium oxalate solution in the ratio of 1 g fiber per 100 mL of the solution at 70-80 • C for three days in a heating mantle. As evaporation went on the loss of water was compensated by adding hot distilled water to keep the level of the solution constant throughout the process. The fibers were then filtered, washed thoroughly with hot distilled water and then dried at 105 • C for constant weight. The loss in weight gave the amount of pectic matters in fiber.

Estimation of Lignin
De-waxed and de-pectinised fibers were dried at 105 • C and then treated with 72% H 2 SO 4 (15 mL for 1 gm of fiber) with frequently stirring at ordinary temperature. The mixture was allowed to keep for 2 h and then diluted to 3% acid concentration. The mixture was refluxed for 4 h. Then, it was allowed to stand over-night and filtered through a sintered funnel, before being dried at 105 • C for constant weight. The weight of the residue gave the amount of lignin content in betel nut fiber.

Estimation of α-Cellulose and Hemicellulose
A suitable amount of de-waxed and de-pectinised fibers were taken to dry at 105 • C. Dried fibers were then treated with sodium chlorite (0.7%) solution buffered at pH 4 in the ratio of 1 g fiber 80 mL liquor at 90-95 • C for 90 min; 1 mL buffer solution of sodium acetate and acetic acid of pH 4 is added for every 10 mL of chlorite solution to stabilize the constant pH. In this process, the chlorite holo-cellulose was collected in the sintered funnel and dried at 105 • C until constant weight was obtained. Chlorite hollo-cellulose was treated with 24% KOH solution for 4 h with occasional stirring (1 g fiber in 100 mL of the alkali solution). By this treatment hemicellulose went into solution and α-cellulose remains undissolved. The α-cellulose was separated by filtration, washed thoroughly with 2% acetic acid solution, finally, with distilled water and dried at 105 • C for constant weight. The obtained weight of α-cellulose was deducted from the weight of holocellulose to calculate the amount of hemicellulose present in fiber.

Extraction of Cellulose from Betel Nut Husk Fibers
To extract cellulose from betel nut fiber, the fibers were immersed in de-ionized water, boiled at 100 • C for three hours, and then washed with de-ionized water. The fiber was then dried in an oven. 5 g of oven dried fiber was placed into a 500 mL Erlenmyner flask, to which 200 mL of de-ionized water (having a temperature of 90 • C) was then added followed by 10 mL of acetic acid and 7.5 g of 80% (w/w) NaClO 2. for 60 min cycle which was repeated for up to 5 cycles. The reaction was stopped by adding cold water. The reaction mixture was then filtered, washed with cold water and acetone and dried at 105 • C in oven until the crucible weight was constant. The holo-cellulose content was calculated. The collected holo-cellulose was treated with 17.5% NaOH solution at room temperature for three hours with occasional stirring to obtain cellulose. The solution mixture was then filtered and washed several times with distilled water. Cellulose was then dried in open air and in oven at 80 • C for five hours.

Preparation of Nanocellulose
Cellulose extracted from betel nut fruit husk fibers was converted to cellulose nano fiber ( Figure 1) by a chemical technique to examine their potential use as reinforcement in bio-composite applications. The cellulose isolated from betel nut fibers were subjected to acid hydrolysis using 62% (w/w) sulfuric acid. The ratio of fiber to acid was 1:8 (w/v) and hydrolysis proceeded under stirring (500 rpm) at 50 • C for 1 h. The reaction mixture was diluted ten times volume with de-ionized water to quench the reaction. The suspension was centrifuged at 8500 rpm for 21-23 min to remove excess acid and water. The precipitated was repeatedly rinsed and centrifuged with deionized water until the suspension remained at neutral pH. The suspension was then sonicated for three hours (optimized) to created cellulose crystals of colloidal dimensions. Cellulose nano fibers were characterized by FTIR, nano zeta seizer, and scanning electron microscopy.

Preparation of Nanocellulose
Cellulose extracted from betel nut fruit husk fibers was converted to cellulose nano fiber ( Figure  1) by a chemical technique to examine their potential use as reinforcement in bio-composite applications. The cellulose isolated from betel nut fibers were subjected to acid hydrolysis using 62% (w/w) sulfuric acid. The ratio of fiber to acid was 1:8 (w/v) and hydrolysis proceeded under stirring (500 rpm) at 50 °C for 1 h. The reaction mixture was diluted ten times volume with de-ionized water to quench the reaction. The suspension was centrifuged at 8500 rpm for 21-23 min to remove excess acid and water. The precipitated was repeatedly rinsed and centrifuged with deionized water until the suspension remained at neutral pH. The suspension was then sonicated for three hours (optimized) to created cellulose crystals of colloidal dimensions. Cellulose nano fibers were characterized by FTIR, nano zeta seizer, and scanning electron microscopy.

Preparation of Cellulose and Nanocellulose Reinforced Polyvinyle Alchohol Composites
Cellulose and nanocellulose of betel nut husk fiber were used to prepare PVA-cellulose and PVA-nanocellulose composites. 10 wt.% of PVA solution was prepared in hot water at 80 °C and the different weight fraction of cellulose and high dispersed nanocellulose suspension were mixed with this solution and stirred at 700 rpm for 30 min, then dispersed by using a homogenizer for 30 min. The mixtures were degassed by allowing them with caps at room temperature overnight. Subsequently, the mixtures were cast in petri dishes and dried at room temperature for several days.

Preparation of Cellulose and Nanocellulose Reinforced Polyvinyle Alchohol Composites
Cellulose and nanocellulose of betel nut husk fiber were used to prepare PVA-cellulose and PVA-nanocellulose composites. 10 wt.% of PVA solution was prepared in hot water at 80 • C and the different weight fraction of cellulose and high dispersed nanocellulose suspension were mixed with this solution and stirred at 700 rpm for 30 min, then dispersed by using a homogenizer for 30 min. The mixtures were degassed by allowing them with caps at room temperature overnight. Subsequently, the mixtures were cast in petri dishes and dried at room temperature for several days. The resulting films were characterized by FTIR and SEM analysis. The mechanical property of the prepared sample was studied by tensile testing and thermal properties were analyzed by TGA and DSC.

Particle Size and Zeta Potential Measurement
The particle size of prepared nano-cellulose was analyzed using Malvern Zeta sizer Nano ZS (Malvern Instruments, Malvern, UK). This equipment uses dynamic light scattering to measure the diffusion of particles moving under Brownian motion and convert this to size and size distribution. It also uses laser Doppler micro electrophoresis to apply an electric filed to the dispersion of particles which then move with a velocity related to their zeta potential.

FTIR Spectroscopy
The FTIR spectrum of cellulose, nanocellulose and their reinforced composites were taken by FTIR spectrometer. Cellulose, nanocellulose and betel nut husk microfibers were used to make pellet with potassium bromide to take FT-IR. On the other hand, FTIR spectra of cellulose, nanocellulose and their reinforced PVA composites were recorded over the frequency range 4000-700 cm −1 using an FTIR spectrometer (PerkinElmer, Boston, MA, USA, Model Forntier, serial no. 101393). FT-IR spectra were obtained in the printed form.

Scanning Electron Microscopy (SEM)
The surface of cellulose, nanocellulose and fracture surface of tensile test sample of cellulose and nanocellulose reinforced PVA composites samples were observed under the field emission scanning electron microscope (JEOL JSM-7600F). The samples were mounted on the carbon tape, which were taped into aluminum plates and coated with ultrathin film of gold with a sputter coater. The images were taken to observe the morphology of cellulose, nano-cellulose and fracture surface of tensile test sample of cellulose and nanocellulose reinforced PVA composites. The photographs are presented in the result and discussion section.

Tensile Properties of the Composites
The tensile test of all prepared cellulose and nanocellulose reinforced PVA composites were measured using a universal tensile testing machine, model: 1410 Titans, England. Tensile tests were conducted following ASTM D 3039/D 3039M-00 (2002) standard method and the cross-head speed of the test was 10 mm/min and gauge length was 50 mm. Each test of the specimen was performed until tensile failure occurred. Six to ten specimens of each composition were tested, and the average values were reported by calculating the maximum five values. The load versus elongation curves were obtained by the instrument. The maximum load values were also recorded by the instrument which can be recalled after the completion of the test. The highest load in the tensile test gave the ultimate strength.

Thermal Properties of Composites
The thermal properties of optimized tensile tested sample were analyzed by Simultaneous 206 Thermal Analyzer (STA), Model No F3 Jupiter serial no STA 449 F-3A-1311-M NETZSCH, Sleb, Germany. The thermo gravimetric analysis and differential scanning calorimetric analysis of the cellulose, nanocellulose and betel nut husk micro fiber reinforced PVA composites were recorded on a STA 449F3 NETZSCH thermal analysis instrument in the temperature range of 30-950 • C and the heating rate was set as 30 • C/10 (K/min)/950 • C in a nitrogen atmosphere. Subsequently, 10 mg of the sample was heated in the aluminum sample pan.

Chemical Constituent of Betel Nut Husk Fiber
Betel nut husk fibers (BNHF) contain cellulose, hemicellulose, lignin and others constituent in small amount. BNHF was extracted and analyzed. The ingredients found in BNHF are presented in Table 1.

FTIR Analysis
Fourier transform infrared (FTIR) analysis is an advanced technique to obtain the structure of a sample. Figure 2 shows the comparative spectra of betel nut husk fiber, cellulose and nanocellulose. As depicted in Figure 2, the broad peak at 3330 cm −1 which appears in al spectra are attributed to the O-H frequency, whereas the peaks at 2893 cm −1 , 2892 cm −1 and 2919 cm −1 predominantly arise from C-H stretching [16,17]. After chemical and ultrasonic treatment, the prominent peak of betel nut husk fiber at 1731 cm −1 corresponds to ester carbonyl vibrations from the acetyl, ferulic and pcoumeric acids of lignin or hemicellulose. Reducing the peaks at 3330 cm −1 and 1731 cm −1 indicates that most of the lignin has been removed from BNHF during the chemical treatment. A stretching peak detected at 1609 cm −1 for unbleached fiber is attributed to the carbonyl group of the acetyl ester in hemicellulose and the carbonyl aldehyde in lignin. The absence of this peak in cellulose and nanocellulose may be due to the removal of lignin and hemicellulose. The 1513 cm −1 and 1428 cm −1 peaks in the BNHF represent aromatic ring vibration and C-H deformation of lignin, respectively. The disappearance of this peak in cellulose indicates the removal of lignin. Peak at 1027 cm −1 , 895 cm −1 in cellulose and 1024 cm −1 , 894 cm −1 in nanocellulose are associated with the C-O stretching and C 1 -H deformation vibration of cellulose [18].

Chemical Constituent of Betel Nut Husk Fiber
Betel nut husk fibers (BNHF) contain cellulose, hemicellulose, lignin and others constituent in small amount. BNHF was extracted and analyzed. The ingredients found in BNHF are presented in Table 1.

FTIR Analysis
Fourier transform infrared (FTIR) analysis is an advanced technique to obtain the structure of a sample. Figure 2 shows the comparative spectra of betel nut husk fiber, cellulose and nanocellulose. As depicted in Figure 2, the broad peak at 3330 cm −1 which appears in al spectra are attributed to the O-H frequency, whereas the peaks at 2893 cm −1 , 2892 cm −1 and 2919 cm −1 predominantly arise from C-H stretching [16,17]. After chemical and ultrasonic treatment, the prominent peak of betel nut husk fiber at 1731 cm −1 corresponds to ester carbonyl vibrations from the acetyl, ferulic and pcoumeric acids of lignin or hemicellulose. Reducing the peaks at 3330 cm −1 and 1731 cm −1 indicates that most of the lignin has been removed from BNHF during the chemical treatment. A stretching peak detected at 1609 cm −1 for unbleached fiber is attributed to the carbonyl group of the acetyl ester in hemicellulose and the carbonyl aldehyde in lignin. The absence of this peak in cellulose and nanocellulose may be due to the removal of lignin and hemicellulose. The 1513 cm −1 and 1428 cm −1 peaks in the BNHF represent aromatic ring vibration and C-H deformation of lignin, respectively. The disappearance of this peak in cellulose indicates the removal of lignin. Peak at 1027 cm −1 , 895 cm −1 in cellulose and 1024 cm −1 , 894 cm −1 in nanocellulose are associated with the C-O stretching and C1-H deformation vibration of cellulose [18].

Scanning Electron Microscopy Analysis (SEM)
The surface of cellulose, nanocellulose and fracture surface of tensile test sample of cellulose and nanocellulose reinforced PVA composites samples were observed under the field emission scanning electron microscope (JEOL JSM-7600F). The SEM images of cellulose, nanocellulose shown in Figure 3 and fracture surface of tensile test sample of cellulose and nanocellulose reinforced PVA composites are shown in Figure 4. The microfibers of cellulose were found as disordered agglomeration position but nanofibers of nanocellulose were found as highly ordered and smooth disagglomeration position in the Figure 3. Disagglomeration of nanofibers makes uniform dispersion of nanofiber and matrix in the nanocomposites. Uniform and good interfacial bonding of fiber and matrix was observed in the nanocellulose-PVA composite in the The surface of cellulose, nanocellulose and fracture surface of tensile test sample of cellulose and nanocellulose reinforced PVA composites samples were observed under the field emission scanning electron microscope (JEOL JSM-7600F). The SEM images of cellulose, nanocellulose shown in Figure  3 and fracture surface of tensile test sample of cellulose and nanocellulose reinforced PVA composites are shown in Figure 4. The microfibers of cellulose were found as disordered agglomeration position but nanofibers of nanocellulose were found as highly ordered and smooth disagglomeration position in the Figure 3. Disagglomeration of nanofibers makes uniform dispersion of nanofiber and matrix in the nanocomposites. Uniform and good interfacial bonding of fiber and matrix was observed in the nanocellulose-PVA composite in the Figure 4.

Measurement of Particle Size and Zeta Potential of Nanocellulose
The particle size of prepared nanocellulose and BNHF nano-fiber were analyzed using Malvern Zeta sizer Nano ZS (Malvern Instruments, UK). The particle size and zeta potential of prepared nano cellulose were measured by the instrument and the results were taken in printed form ( Figures A1-A6 in appendix). The time of acid hydrolysis and effect of sonication on particle size was studied. In optimized acid concentration was 62% (w/w), reaction time one hour at 50 °C temperature. The reaction temperature, acid concentration and reaction time were optimized by conducting a series of reactions. If the reaction temperature is low (25 °C), then the reaction process toke place over a long time, and the particle size distribution report showed that without sonication the average particle size after hydrolysis was 117.6 nm. After three hours sonication, the average size was found 68.27 nm. The zeta potential of prepared nano cellulose was −39.1 mV and the colloidal nano suspension was very stable. The sonication time decreased the zeta potential and it was −19.7. Analytical reports of prepared nano cellulose are presented in appendix section (Figures A1-A6).

Tensile Properties of Composites
The effect of fiber loading (wt%) on tensile strength and elongation at break of cellulose and nanocellulose reinforced polyvinyle alcohol composites along with their error bars are given in Figures 5 and 6. From these figure the increases of tensile strength with increasing the fiber loading (wt%) up to 2% fiber for both cellulose and nanocellulose reinforced PVA composite then decreases. Nanocellulose reinforced PVA composite showed higher tensile strength than cellulose-PVA

Measurement of Particle Size and Zeta Potential of Nanocellulose
The particle size of prepared nanocellulose and BNHF nano-fiber were analyzed using Malvern Zeta sizer Nano ZS (Malvern Instruments, UK). The particle size and zeta potential of prepared nano cellulose were measured by the instrument and the results were taken in printed form ( Figures A1-A6 in Appendix A). The time of acid hydrolysis and effect of sonication on particle size was studied. In optimized acid concentration was 62% (w/w), reaction time one hour at 50 • C temperature. The reaction temperature, acid concentration and reaction time were optimized by conducting a series of reactions. If the reaction temperature is low (25 • C), then the reaction process toke place over a long time, and the particle size distribution report showed that without sonication the average particle size after hydrolysis was 117.6 nm. After three hours sonication, the average size was found 68.27 nm. The zeta potential of prepared nano cellulose was −39.1 mV and the colloidal nano suspension was very stable. The sonication time decreased the zeta potential and it was −19.7. Analytical reports of prepared nano cellulose are presented in appendix section (Figures 1 and A2-A6).

Tensile Properties of Composites
The effect of fiber loading (wt%) on tensile strength and elongation at break of cellulose and nanocellulose reinforced polyvinyle alcohol composites along with their error bars are given in Figures 5 and 6. From these figure the increases of tensile strength with increasing the fiber loading (wt%) up to 2% fiber for both cellulose and nanocellulose reinforced PVA composite then decreases. Nanocellulose reinforced PVA composite showed higher tensile strength than cellulose-PVA composite which indicate the good dispersion of nano fiber in PVA matrix and good interfacial adhesion between PVA and nanocellulose. Nanocellulose reinforcement in PVA composite enhanced the tensile strength of composites. 2% cellulose and nanocellulose reinforced PVA composite give the highest tensile strength. Elongation at break decreases when increasing the fiber loading of composite, but cellulose reinforced PVA composites showed higher elongation at break. composite which indicate the good dispersion of nano fiber in PVA matrix and good interfacial adhesion between PVA and nanocellulose. Nanocellulose reinforcement in PVA composite enhanced the tensile strength of composites. 2% cellulose and nanocellulose reinforced PVA composite give the highest tensile strength. Elongation at break decreases when increasing the fiber loading of composite, but cellulose reinforced PVA composites showed higher elongation at break.

Thermal Properties of Composites
In order to understand the thermal stability of cellulose, nanocellulose, PVA, and its cellulose and nano-composites, TGA measurements were carried out. Both TGA thermographs of all PVA and their nano-composites show similar patterns, i.e., three main weight loss regions. The first region (75-160 °C) is due to the evaporation of water, and the weight loss of the film in these ranges is about 5-10 wt.%. The second transition region (260-390 °C) is due to the structural degradation of PVA nanocomposite films and the total of weight loss in this range was approximately 74 wt.%. The third region occurred above 390 °C due to the cleavage backbone of PVA bio composite films or the decomposition of carbonaceous matter. The total weight loss in this range was more than 95 wt.% at composite which indicate the good dispersion of nano fiber in PVA matrix and good interfacial adhesion between PVA and nanocellulose. Nanocellulose reinforcement in PVA composite enhanced the tensile strength of composites. 2% cellulose and nanocellulose reinforced PVA composite give the highest tensile strength. Elongation at break decreases when increasing the fiber loading of composite, but cellulose reinforced PVA composites showed higher elongation at break.

Thermal Properties of Composites
In order to understand the thermal stability of cellulose, nanocellulose, PVA, and its cellulose and nano-composites, TGA measurements were carried out. Both TGA thermographs of all PVA and their nano-composites show similar patterns, i.e., three main weight loss regions. The first region (75-160 °C) is due to the evaporation of water, and the weight loss of the film in these ranges is about 5-10 wt.%. The second transition region (260-390 °C) is due to the structural degradation of PVA nanocomposite films and the total of weight loss in this range was approximately 74 wt.%. The third region occurred above 390 °C due to the cleavage backbone of PVA bio composite films or the decomposition of carbonaceous matter. The total weight loss in this range was more than 95 wt.% at 500 °C. Figures 7-10 shows that all PVA-cellulose and PVA-nanocellulose composites start to

Thermal Properties of Composites
In order to understand the thermal stability of cellulose, nanocellulose, PVA, and its cellulose and nano-composites, TGA measurements were carried out. Both TGA thermographs of all PVA and their nano-composites show similar patterns, i.e., three main weight loss regions. The first region (75-160 • C) is due to the evaporation of water, and the weight loss of the film in these ranges is about 5-10 wt.%. The second transition region (260-390 • C) is due to the structural degradation of PVA nanocomposite films and the total of weight loss in this range was approximately 74 wt.%. The third region occurred above 390 • C due to the cleavage backbone of PVA bio composite films or the decomposition of carbonaceous matter. The total weight loss in this range was more than 95 wt.% at 500 • C. Figures 7-10 shows that all PVA-cellulose and PVA-nanocellulose composites start to degrade at higher temperatures than those of PVA. This indicates that the addition of cellulose and nanocellulose fiber can improve thermal stability of PVA, thus confirming the enhanced thermal stability due to a strong hydrogen bonding between the hydroxyl groups of nanocellulose and the PVA matrix.

Conclusions
The optimized parameters of the extraction and synthesis of nanocellulose from BNHF have been developed. Nanocellulose having a diameter of 68-117 nm were obtained from macroscopic and microscopic forms of cellulose following strong acid hydrolysis and a sonication method. This was proven by particle size analyses, FTIR, SEM, and thermal characterization. The effects of cellulose and nanocellulose reinforcing in PVA matrix have been investigated. Two series of bio composites of cellulose-PVA and nanocellulose-PVA were prepared and characterized. The tensile, thermal, and morphological properties of nanocellulose-PVA nanocomposites showed higher values than cellulose-PVA composites. These materials can be used for biomedical applications and provide an opportunity for the efficient utilization of waste betel nut husk fiber.

Conclusions
The optimized parameters of the extraction and synthesis of nanocellulose from BNHF have been developed. Nanocellulose having a diameter of 68-117 nm were obtained from macroscopic and microscopic forms of cellulose following strong acid hydrolysis and a sonication method. This was proven by particle size analyses, FTIR, SEM, and thermal characterization. The effects of cellulose and nanocellulose reinforcing in PVA matrix have been investigated. Two series of bio composites of cellulose-PVA and nanocellulose-PVA were prepared and characterized. The tensile, thermal, and morphological properties of nanocellulose-PVA nanocomposites showed higher values than cellulose-PVA composites. These materials can be used for biomedical applications and provide an opportunity for the efficient utilization of waste betel nut husk fiber.

Conclusions
The optimized parameters of the extraction and synthesis of nanocellulose from BNHF have been developed. Nanocellulose having a diameter of 68-117 nm were obtained from macroscopic and microscopic forms of cellulose following strong acid hydrolysis and a sonication method. This was proven by particle size analyses, FTIR, SEM, and thermal characterization. The effects of cellulose and nanocellulose reinforcing in PVA matrix have been investigated. Two series of bio composites of cellulose-PVA and nanocellulose-PVA were prepared and characterized. The tensile, thermal, and morphological properties of nanocellulose-PVA nanocomposites showed higher values than cellulose-PVA composites. These materials can be used for biomedical applications and provide an opportunity for the efficient utilization of waste betel nut husk fiber.
Author Contributions: T.S. contributed on the experimental works. T.S. and S.S. contributed on the analytical works. H.P.N. and M.W.K. supervised the research works and discussed the data. T.S. wrote the paper discussing with all authors. All authors have read and agreed to the published version of the manuscript.
Funding: This research received no external funding.
Author Contributions: T.S. contributed on the experimental works. T.S. and S.S. contributed on the analytical works. H.P.N. and W.K. supervised the research works and discussed the data. T.S. wrote the paper discussing with all authors. All authors have read and agreed to the published version of the manuscript.