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Journal of Nanomaterials

Volume 2014 (2014), Article ID 702538, 9 pages

http://dx.doi.org/10.1155/2014/702538
Research Article

Isolation, Characterization, and Application of Nanocellulose from Oil Palm Empty Fruit Bunch Fiber as Nanocomposites

1Department of Chemical Engineering, Universiti Teknologi Malaysia, 81310 Skudai, Johor, Malaysia

2Institute of Hydrogen Economy, Faculty of Chemical Engineering, Universiti Teknologi Malaysia, 81310 Johor Bahru, Johor, Malaysia

Received 21 April 2014; Revised 3 June 2014; Accepted 3 June 2014; Published 8 July 2014

Academic Editor: Prashant Kumar

Copyright © 2014 N. S. Lani et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Nanocomposites, consisting of a polymeric matrix and nanosized elements as reinforcement, have attracted significant scientific attention because of their high mechanical performance. A large variety of nanocomposites have been prepared using bio-based materials as a matrix and nanoreinforcement, so that it can reduce the dependence on nondegradable products and move to a sustainable materials basis. The objective of this study was to isolate nanocellulose from empty fruit bunch (EFB) fiber and their reinforcing effect on polyvinyl alcohol (PVA)/starch blend films. A series of PVA/starch films with different content of nanocellulose were prepared by solution casting method. Nanocellulose fiber with diameters ranging from 4 to 15 nm has been successfully prepared. On the other hand, PVA/starch films reinforced with nanocellulose fiber possess significantly improved properties compared to unreinforced film. From the results, PVA/starch films with the addition of 5% (v/v) of nanocellulose exhibited best combination of properties. This nanocomposite was found to have tensile strength at about 5.694 MPa and elongation at break was 481.85%. In addition to good mechanical properties, this nanocomposite has good water resistance and biodegradability.

1. Introduction

Nowadays, the demands of plastics materials are increasing rapidly, especially in food packaging application. Packaging is used to keep the product from surrounding and to maintain the food product quality. The levels of chemical migration from the packaging have to be lower than control safe level [1], or otherwise the food might be contaminated and consequently risks the consumer safety. Moreover, another issue and consideration is the severe problems created by food packages to the environment since most of these products are not normally environmentally friendly and nonbiodegradable.

The use of polyvinyl alcohol (PVA) particularly in commercial industry has arisen worldwide. This is due to their unique chemical and physical properties, as well as being nontoxic, highly crystalline, and water-soluble polymer and having good film-forming and high hydrophilic properties. Furthermore, PVA is highly recognized as a biodegradable polymer. However, the main disadvantage of PVA is their price which is quite expensive. Therefore, PVA can be blended with other natural polymers in order to reduce the materials costs and thus make PVA more economical to use.

Starch is one of the most widely used in blends with PVA as PVA/starch blend would increase biodegradability of PVA. It has been scientifically proven through extensive worldwide studies by many researchers [24] and by Ishigaki et al. [5]. Tang and Alavi [6] mentioned that both starch and polyvinyl alcohol are polar substances that have hydroxyl groups in their chemical structure, which are able to form intermolecular and intramolecular hydrogen bond. However, the major disadvantages of these PVA/starch blends are particularly poor water barrier properties, generally attributed to the very large number of hydroxyl groups along with their intrinsic hydrophilicity. Therefore, several studies proposed the incorporation of fillers in a nanoscale size into PVA/starch blends in order to improve their water barrier properties.

Most of the previous studies have investigated the use of nanofillers such as nanosilicon dioxide [7, 8], montmorillonite clay [9, 10], sodium montmorillonite clay [11], and nanoparticles of poly(methyl methacrylate-co-acrylamide) [12]. However, these nanoparticles had no significant influence on biodegradability of films. For that reason, this research was conducted for the purpose of improvement in the properties of PVA and starch blend by using nanocellulose from EFB fiber as reinforcement. Furthermore, very limited studies have been reported concerning the nanocellulose reinforced PVA/starch blend films compared to other fillers.

Cellulose extracted from empty fruit bunch (EFB) fiber has attracted growing interest because of their unique characteristics, including low cost, lower density, high specific strength, good thermal properties, and biodegradable. Oil palm EFB fiber is a natural fiber which has great relevance to Malaysia, as a large quantity of the biomass is generated by oil palm industries. The total amount of EFB produced was estimated to be more than 10 million tons per year, whereby only 10% of the EFB is used and the rest are abundant [13].

Natural fibers are mainly composed of cellulose, hemicellulose, and lignin. Generally, the EFB fiber contains about 40–50% cellulose, 20–30% hemicellulose, and 20–30% lignin with moisture content of about 10–15%, which has highest composition of cellulose compared to coir, corn, bagasse, and kenaf fiber. Furthermore, a comprehensive research and review article dealing with isolation of cellulose fiber in nanoparticle size by sulfuric acid hydrolysis was published by many researchers [1422].

Besides food packaging applications, nanocomposites based on polymer matrix have a great potential for a broad range of application fields such as automotive, aerospace, optoelectronics, and biomedical industry. Owing to their nanoscale size features and high aspect ratio, they not only possess excellent mechanical properties comparable to composite reinforced with microsized fillers, but they also display outstanding combination of optical, electrical, thermal, magnetic, and other physic-chemical properties.

The aims of this study were to isolate nanocellulose from EFB fiber via acid hydrolysis process. The properties of untreated and nanocellulose fiber were investigated using Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), and thermogravimetric (TG) analysis. The morphology of the isolated nanofibers was also characterized using transmission electron microscopy (TEM) analysis. The effect of nanocellulose content, isolated from EFB fiber, on the properties of PVA/starch films was also explored.

2. Experimental

2.1. Materials and Chemicals

Empty fruit bunch fibers were collected from Johor, Malaysia, and were used as raw material in this study. Sodium chlorite, acetic acid, sodium sulfite, sodium hydroxide, sulfuric acid, polyvinyl alcohol, starch, and glycerol meanwhile were purchased from Sigma-Aldrich. All the chemicals are reagent grade and were used as received.

2.2. Isolation of Nanocellulose

A 0.7% (w/v) sodium chlorite (NaClO2) solution was prepared and then acetic acid was added to acidify the NaClO2 solution until the pH reached 4. The fibers were boiled in NaClO2 solution for 2 hours at 70–80°C whereby the ratio of fiber to NaClO2 solution was set to 1 : 50. The bleaching process was repeated for four or five times until fiber became white and then filtered. After being filtered, the residue was washed for several times with distilled water and dried in air. The bleached cellulose obtained was heated to about 70 to 80°C in 5% (w/v) sodium sulfite solution for 2 hours. The fibers were filtered, washed, and dried in air. After being dried, the fibers were treated in 17.5% (w/v) sodium hydroxide (NaOH) solution for 2 hours. The residue was washed for several times with distilled water and dried in air.

After alkali treatment of fibers, the cellulose materials were hydrolyzed in 64 wt% sulfuric acid solution under strong agitation at 45°C for 45 minutes. Then, cold water was added to stop the reaction. The diluted suspension was then centrifuged at 11000 rpm for 10 minutes to obtain precipitate. This process was repeated until the pH of the suspension reach 5 then dialysis was carried out for 3 days.

2.3. Preparation of Nanocomposite

An aqueous solution containing PVA, starch, glycerol, and nanocellulose fiber were used to cast the film. The PVA and starch solution (70 : 30 wt%) were prepared by dissolving PVA powder in 100 mL distilled water at 97°C for 30 minutes, while being stirred with a mechanical stirrer until PVA particles were completely dissolved in water. After the PVA had fully dissolved, starch was then added and the mixture is again heated and stirred at 97°C for 30 minutes [23]. Glycerol was added to the mixed solution at a 30 wt% ratio based on total weight of starch and PVA [24]. Five sets of nanocomposites with a nanocellulose content of 5, 10, 15, and 20% (v/v) with respect to the volume of PVA and starch solution were prepared. A solution of 5 g mixed polymer was cast on Petri-dish plate and allow it to dry at room temperature for 2 days. After the film is completely dry, the film was peeled off from the plate.

2.4. Fourier Transform Infrared Spectroscopy

FTIR spectra of raw EFB and nanocellulose fibers were obtained by using Spectrum One-Perkin Elmer with software spectrum v5.02. The fibers were crushed into small particles and then blended with potassium bromide (KBr) followed by pressing the mixture into ultrathin pellets. In this analysis, ratio of fiber to KBr was approximately 1 : 99. A total of 100 scans were recorded in the range 370–4000 cm−1 with a resolution of 2 cm−1 for each sample.

2.5. X-Ray Diffraction

The XRD patterns for fibers and composite films were measured using Ni-filter Cu Kα radiation, with a wavelength of 0.1541 nm at 40 kV and 40 mA. Powder samples were scanned in 2θ range varying from 10° to 50°. Equation (1) was used to calculate the crystallinity index of the fibers: where is the height of the 200 peak, which represents both crystalline and amorphous material while is the lowest height between the 200 and 110 peaks, which represents amorphous material.

2.6. Scanning Electron Microscopy

The surface morphology of the film samples was investigated by using a JEOL JSM-6390LV scanning electron microscope, with the accelerating voltage of 50 kV. All specimens were coated with gold and then observed.

2.7. Transmission Electron Microscopy

TEM images were obtained using a JEM-2100 transmission electron microscope operated at 120 kV. For TEM sample preparation, the nanocellulose particles were deposited on a carbon-coated grid by placing a drop of a very dilute cellulose nanofiber suspension on the grid and then allowed to dry in order to evaporate the liquid.

2.8. Mechanical Properties

The tensile strength and elongation at break of the composite films were measured on the 2.5 kN Lloyd tensile tester according to the ASTM D882. Samples with rectangular shape were cut into 60 mm × 13 mm strips from the films. The cut films were conditioned at the temperature and relative humidity of 23 ± 2°C and 50 ± 10%, respectively, for more than 40 hours prior to measurement of mechanical properties. Tensile testing was conducted at a cross-head speed of 10 mm/minute and a gauge length of 40 mm. Six samples were tested for each set and averaged.

2.9. Water Absorption Properties

The water absorption capacity of the composite films was measured by drying the film in a vacuum oven at 50°C for 24 hours. Then, the film was cooled in desiccator and immediately weighted. The conditioned film was fully immersed in distilled water for 5 minutes. Subsequently, the remaining water on the surface of film was removed by using filter paper and immediately weighted. All measurements were performed for four specimens and averaged. The water absorption capacity was calculated using the following: where is the weight of film after being immersed in distilled water and is the initial dry weight of the film.

2.10. Soil Burial Degradation Properties

The films were cut into 50 mm × 50 mm strips and then were weighted. The degradation test was carried out by burying the films in the soil placed in a flower pot at the depth of 5 cm. The humidity, temperature, and moisture values were negligible and do not require any adjustment in order to provide a realistic environment, where soil humidity, temperature, and type and amount of microorganisms are in less control and change with weather. At a 15-day interval, the films were taken out carefully from the soil. The remaining soil on the surface of the film was removed and then weighted. The degradation rate in the soil burial test was determined by calculating the weight loss of the films with time using the following: where is the dry weight of the specimen after being buried in the soil and is the initial dry weight of the specimen.

3. Results and Discussion

3.1. Fourier Transform Infrared Spectroscopy

The FTIR spectra spectroscopy is an indispensable technique for tracking changes in the chemical structures of the fibers after the various treatments which they received. The FTIR spectra of the raw EFB fiber and nanocellulose fibers are shown in Figure 1.

702538.fig.001
Figure 1: FTIR spectra of (a) untreated fiber and (b) nanocellulose fiber.

As shown in Figure 1, untreated and treated fibers presented two main regions of absorbance; the first one at low wavelengths (500–1750 cm−1) and the second one at higher wavelengths (2800–3500 cm−1). This observation is in agreement with the study done by Morán et al. [15]. The absorption peaks located in the ranges 3300–3450 cm−1 and 2890–2900 cm−1 in both samples are attributed to the hydroxyl group and aliphatic saturated C–H stretching vibration, respectively [15, 25, 26]. The peaks appearing from 1330 to 1360 cm−1 are due to the bending vibration of the C–H and C–O groups in the polysaccharide aromatic rings in cellulose, hemicelluloses, and lignin [27]. Meanwhile, stretching of C–O and O–H was reflected by peaks appearing in the region 1050–1070 cm−1 [28] and the peak at 1055 cm−1 is due to the bending vibration of the C–O–C pyranose ring [14].

Stretching vibrations of C=C bonds in the lignin are found in the 1608–1623 cm−1, whereby the peak at 1623 cm−1 is caused by vibrations of C=C bonds in the benzene stretching ring. Meanwhile, the vibration of the aromatic rings can be seen at 1608 cm−1 in the spectra of the untreated fiber, which is attributed to the C=C stretching of the carboxyl groups [28]. In addition, lignin presented characteristic peak at 1432 cm−1 was due to the presence of methoxy-O-CH3, while the vibration peak at 1259 cm−1 has been related to the C–O–C stretching of the aryl-alkyl ether [29]. Disappearance of all these peaks from the spectra of the treated fibers can be ascribed to treatment of the EFB fibers with sodium hydroxide followed by acid hydrolysis as these treatments are known to remove most of the lignin from the EFB fibers.

Furthermore, the most noticeable difference between spectra of the untreated fiber and those of the chemically treated ones is disappearance of the vibration peak observed at 1736 cm−1 from the spectra of the alkali treated fibers. This peak is also absent in the sulfuric acid hydrolysed cellulose. The peak observed at 1736 cm−1 in the spectra of the untreated fibers is likely to be associated with the C=O stretching in the acetyl and uronic ester groups of hemicelluloses or the ester carbonyl groups in the p-coumaric units of the lignin. Another possibility is that carboxyl or aldehyde absorption could be arising from the opened terminal glucopyranose rings or oxidation of the C–OH groups [30, 31]. This peak has disappeared from the spectra of cellulose fibers and it is believed to be due to removal of hemicellulose by alkali treatment.

By comparing the spectra of the untreated and treated EFB fibers, the peak presents at 1646 cm−1 corresponding to the treated fibers is related to the absorption of water by cellulose. Appearance of this peak in the spectra of the cellulose fibers is probably due to reaction of sodium hydroxide with the hydroxyl groups of celluloses and subsequent formation of water molecules [27]. As pointed out by Abraham et al. [32], even though the treated fibers were subjected to the drying process, the water adsorbed in the cellulose molecules is very difficult to be extracted due to the cellulose-water interaction.

From the FTIR analysis, it has been concluded that almost all the lignin and hemicelluloses were removed after chemical treatment. This arises from the absence of the absorption bands in-between 1500 and 1600 cm−1 and 1730 and 1740 cm−1, which relates to the lignin and hemicelluloses components, respectively. Therefore, it can be stated that the nanocellulose obtained in this study was almost pure, which contains a very small amounts of lignin and other noncellulosic substances.

3.2. X-Ray Diffraction

The X-ray diffraction patterns of the untreated and treated EFB fiber are shown in Figure 2 meanwhile the diffraction patterns of PVA/starch film and PVA/starch reinforced with nanocellulose composite film are shown in Figure 3.

702538.fig.002
Figure 2: X-ray diffraction patterns for (a) untreated fiber and (b) nanocellulose fiber.
702538.fig.003
Figure 3: X-ray diffraction patterns for (a) PVA/starch blend film and (b) PVA/starch reinforced with 5% (v/v) nanocellulose composite film.

As can be seen in Figure 2, both fibers had diffraction peaks at around and , representing the presence of crystalline and amorphous cellulose structure, respectively. The crystallinity index of untreated EFB fiber (calculated by Segal formula) was approximately 38% while that of nanocellulose fiber was estimated 73%. By comparing the results, nanocellulose from EFB fiber obtained in this study exhibited higher crystallinity than those produced by Fahma et al. [33] and Jonoobi et al. [31], which is around 59 and 69%, respectively. According to Jonoobi et al. [31], the higher crystallinity of nanofiber was due to the peeling reactions that take place in the amorphous areas during the hydrolysis process. Because of the ability of sulfuric acid to penetrate into the amorphous region, the glycosidic bonds were cleaved under hydrolytic conditions and finally releasing individual crystallites [34, 35].

Generally, cellulose in natural fibers comes in four types of cellulose that are classified as types I, II, III, and IV. It is interesting to note that the untreated EFB fiber shows typical cellulose I structure, based on the fact that there is no doublet in the main peak at [36, 37]. After treating the EFB fiber with sodium hydroxide and sulfuric acid, the crystalline peak appears as a doublet at and , representing transformation of native cellulose from cellulose I to cellulose II. A significant variation in the diffraction pattern of untreated and cellulose fibers can be explained by the replacement of OH groups by ONa groups during alkaline treatment. Subsequent rinsing with water will remove the linked Na-ions and thus causing the cellulose to be converted to a new crystalline structure, which is cellulose II [38].

Meanwhile, based on the XRD diffractogram shown in Figure 3, the crystallinity indexes of PVA/starch blend films and PVA/starch reinforced with nanocellulose composite film were found to be 30.77 and 50.38%, respectively. It has been shown that the presence of nanocellulose fibers in the blend film essentially increased the crystallinity of the composite film. The reason of the increment of crystallinity was due to the nucleation effects, whereby the nanocelluloses were acted as an agent of nucleation for the crystal growth [39]. The crystalline regions of the composites behave as barriers and any change in crystallinity may affect the final properties of the composite. Since PVA/starch nanocomposite film has a higher degree of crystallinity than blend film, a higher water resistance would be expected, as water absorption occurs almost entirely in the amorphous region of a polymeric system [40].

3.3. Transmission Electron Microscopy

Figure 4 shows the TEM micrograph of a dilute suspension of nanocellulose from EFB fiber prepared by acid hydrolysis.

702538.fig.004
Figure 4: TEM image of nanocellulose from EFB fiber.

The analysis of the TEM micrograph revealed that the aqueous suspension of nanocellulose fiber consist of rod-like nanoparticles, whereby there were some nanoparticles agglomerated in the forms of bundles while some of them were well separated. According to Othman et al. [41], agglomeration is generally due to the Van der Waals attraction forces between nanoparticles. Moreover, it can be seen that the diameter of the nanocellulose fiber was found to be in the range of 4–15 nm. Interestingly, the diameter of the nanocellulose obtained in this study was smaller than those produced by an acid hydrolysis from different sources such as cotton linter (14.6 ± 3.9 nm) by Roohani et al. [42], microcrystalline cellulose (28 ± 9 nm) by Bilbao-Sainz et al. [43], and sisal fiber (30.9 ± 12.5 nm) by Morán et al. [15] as well as those produced by mechanical treatment originating from rutabaga fiber [36], bamboo fiber [44], and rubberwood [31], for which the range of diameter has been reported as 5–20 nm, 30–80 nm, and 10–90 nm, respectively.

3.4. Scanning Electron Microscopy

The surface morphology of the composite film was also studied by SEM analysis. Figure 5 shows the electron micrograph for the surface of PVA/starch composite film with 5% and 20% (v/v) nanocellulose content. It can be seen that the nanocellulose fibers at low content were better dispersed in the PVA/starch matrix, as there is no rough surface or large agglomerates (Figure 5(a)). Meanwhile, agglomeration of nanocellulose was observed at PVA/starch composite film with 20% (v/v) nanocellulose content, which contributes to poor final properties of composite films.

fig5
Figure 5: SEM image of PVA/starch composite film with (a) 5% (v/v) and (b) 20% (v/v) nanocellulose content.
3.5. Mechanical Properties

Figure 6 indicates the effect of nanocellulose content on tensile strength and elongation at break of the nanocomposite films.

702538.fig.006
Figure 6: The dependence of the tensile strength and elongation at break on the nanocellulose content.

From Figure 6, it is observed that the tensile strength of the PVA/starch blend film was 3.830 MPa. When nanocellulose fiber was added into the PVA and starch solution, the tensile strength was increased along with an increase in nanocellulose content, and the highest tensile strength occurred at 10% (v/v), which was around 7.094 MPa. When the nanocellulose content exceeded 10% (v/v), the tensile strength of the blend film decreased along with an increase in nanocellulose content, but it was still much higher than that of the unreinforced film.

The same trend from addition of nanocellulose fiber content can also be found for the elongation at break. It was found that the elongation at break had the highest value when 5% (v/v) nanocellulose was used during the nanocomposite preparation, whereby the elongation at break of the nanocomposite film increased by 30.54% in comparison to the unreinforced film. An addition of 10% (v/v) nanocellulose content however had deterioration effect for elongation at break as a sharp decrease was observed from 481.85% to 312.18%. Then, the elongation at break of the nanocomposite film decreased slowly from 312.18% to 288% along with an increase in nanocellulose content from 10% to 20% (v/v).

The enhancement in tensile strength and elongation at break at low content of fillers was due to very fine nature of nanocellulose fiber and well dispersion of nanocellulose through the PVA/starch matrix. Meanwhile, according to Das et al. [24], the remarkable increase in the mechanical properties indicated the presence of intermolecular interactions between nanocellulose and PVA or nanocellulose and starch, which disturbs the interchain force of attraction of the PVA/starch. On the other hand, the reason of the reduction of tensile strength and elongation at break was the fact that the excess amount of nanocellulose fiber leads to an increase in intermolecular interaction that might compete with interactions between PVA, starch, and nanocellulose fiber. Therefore, the miscibility and compatibility of PVA, starch, and nanocellulose were reduced, which decreased the tensile strength and elongation at break of nanocomposite films.

3.6. Water Absorption Properties

Figure 7 shows that the water absorption capacity of PVA/starch/nanocellulose composite films depended on the amount of nanocellulose loading.

702538.fig.007
Figure 7: Percentage of water absorption capacity for PVA/starch reinforced with nanocellulose fiber at different amount.

Comparing the water absorption capacity of PVA/starch blend film and nanocellulose fiber reinforced PVA/starch composite, it is noted that the percentage of water absorption of all nanocellulose fiber reinforced films was lower, indicating that films that contain nanocellulose have a good preventive ability against water. This result illustrates that the water absorption properties were improved by the presence of nanocellulose fiber in the blend films. The possible reason for this kind of behavior was related to the formation of the network structure between the nanocellulose particles and PVA/starch components, which prevented the water molecules from dissolving and improved the water resistance of the film. The presence of the nanocellulose fibers means that the pathway for water molecules to diffuse into the composites is altered from the direct diffusion to a tortuous path, which leads to the improvement in water barrier properties. Meanwhile, Alhuthali et al. [45] in their study stated that the high aspect ratio of nanocellulose may have also contributed to a reduction in absorbed water.

Some differences are observed by increasing nanocellulose content in PVA/starch blend films during water absorption tests. By comparison, an increment of water absorption capacity was observed with increasing nanocellulose content, which is possibly due to the poor dispersion of the nanocellulose fiber (Figure 5). It can be observed that the water absorption of PVA/starch/nanocellulose films increased from 19.71 to 31.06% with cellulose content from 5% to 20% (v/v). It can be explained by the formation of some large accumulated particles, whereby the large accumulation of nanocellulose particles can generate voids which can absorb water molecules and therefore increase the percentage of water absorption [46].

3.7. Soil Burial Degradation Properties

Degradability of composites is important when a polymeric system is applied in daily lives as its weight loss degree has a direct influence on the environment. In this study, the effect of different amount of nanocellulose fiber on film weight loss rate was conducted via soil burial test and the results were presented in Figure 8.

702538.fig.008
Figure 8: Degradability of PVA/starch nanocomposite films in the soil burial test.

Results showed that the degradation rate of PVA/starch blend film was higher than PVA/starch films that contained nanocellulose fiber, whereby the PVA/starch blend films without the addition of nanocellulose were able to lose its weight up to 59.39% after being buried for 90 days. It is believed that the faster disintegration of PVA/starch blend films can be explained by the ability of composite film to absorb higher amount of water. This is because the water absorbed by the films caused the microorganisms such as algae, bacteria, and fungi to attach and grow, since the films have become the main energy sources of the microbial growth. This result is consistent with the result from water absorption test of PVA/starch nanocomposite films reflected in Figure 8 and thus illustrates that the addition of nanocellulose fiber prevented water to be diffused into the films and the growth of microorganism occurred slowly. Furthermore, the study also found that the degradation rate of PVA/starch nanocomposite after being buried for 90 days is slightly lower than that of the PVA/starch blend film.

4. Conclusion

In this study, cellulose and nanocellulose were successfully extracted from palm oil EFB fiber. It has been proved that alkali treatment seems to be effective in the removal of lignin and hemicelluloses components. In addition, the chemical treatment used in this study was able to achieve improvement in the properties of cellulose and nanocellulose, compared to that observed in previous studies. Evidence of noncellulosic components loss can be observed in the FTIR spectra, whereby there is no main absorption band of lignin and hemicelluloses at 1500–1600 cm−1 and 1730–1740 cm−1 after treating with NaOH. On the other hand, the crystallinity index of the fiber increases after each treatment. Higher crystallinity value of the fiber is expected to provide better reinforcement and therefore better properties of the composite films. TEM observation revealed that acid hydrolysis was able to produce nanocellulose from EFB fiber with a diameter in the range of 4–15 nm.

Successful improvements of nanocellulose reinforced PVA/starch film can be seen in terms of mechanical and water absorption properties due to the good compatibility between the nanocellulose and the polymer matrix. Furthermore, the properties of nanocomposite films were also affected by different nanocellulose content. The reinforcement effect at low nanocellulose content in the PVA/starch matrix is much stronger because the excess nanocellulose tended to agglomerate. The PVA/starch reinforced with nanocellulose fiber had a tensile strength, elongation at break, and water absorption capacity of approximately 5.694 MPa, 481.85%, and 19.71% at an addition of 5% (v/v) nanocellulose content.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

References

  1. K. A. Barnes, R. Sinclair, and D. Watson, Chemical Migration and Food Contact Materials, Elsevier B.V., Woodhead, UK, 1st edition, 2007.
  2. M. A. L. Russo, R. Truss, and P. J. Halley, “The enzymatic hydrolysis of starch-based PVOH and polyol plasticised blends,” Carbohydrate Polymers, vol. 77, no. 3, pp. 442–448, 2009. View at Publisher · View at Google Scholar · View at Scopus
  3. N. Tudorachi, C. N. Cascaval, M. Rusu, and M. Pruteanu, “Testing of polyvinyl alcohol and starch mixtures as biodegradable polymeric materials,” Polymer Testing, vol. 19, no. 7, pp. 785–799, 2000. View at Publisher · View at Google Scholar · View at Scopus
  4. Y. Yun, Y. J. Wee, H. S. Byun, and S. D. Yoon, “Biodegradability of chemically modified starch (RS4)/PVA blend films: part 2,” Journal of Polymers and the Environment, vol. 16, no. 1, pp. 12–18, 2008. View at Publisher · View at Google Scholar · View at Scopus
  5. T. Ishigaki, Y. Kawagoshi, M. Ike, and M. Fujita, “Biodegradation of a polyvinyl alcohol-starch blend plastic film,” Journal of Microbiology and Biotechnology, vol. 15, no. 3, pp. 321–327, 1999.
  6. X. Tang and S. Alavi, “Recent advances in starch, polyvinyl alcohol based polymer blends, nanocomposites and their biodegradability,” Carbohydrate Polymers, vol. 85, no. 1, pp. 7–16, 2011. View at Publisher · View at Google Scholar · View at Scopus
  7. S. Tang, P. Zou, H. Xiong, and H. Tang, “Effect of nano-SiO2 on the performance of starch/polyvinyl alcohol blend films,” Carbohydrate Polymers, vol. 72, no. 3, pp. 521–526, 2008. View at Publisher · View at Google Scholar · View at Scopus
  8. Z. Abbasi, “Water resistance, weight loss and enzymatic degradation of blends starch/polyvinyl alcohol containing SiO2 nanoparticle,” Journal of the Taiwan Institute of Chemical Engineers, vol. 43, no. 2, pp. 264–268, 2012. View at Publisher · View at Google Scholar · View at Scopus
  9. K. Majdzadeh-Ardakani and B. Nazari, “Improving the mechanical properties of thermoplastic starch/poly(vinyl alcohol)/clay nanocomposites,” Composites Science and Technology, vol. 70, no. 10, pp. 1557–1563, 2010. View at Publisher · View at Google Scholar · View at Scopus
  10. I. Spiridon, M. C. Popescu, R. Bodârlǎu, and C. Vasile, “Enzymatic degradation of some nanocomposites of poly(vinyl alcohol) with starch,” Polymer Degradation and Stability, vol. 93, no. 10, pp. 1884–1890, 2008. View at Publisher · View at Google Scholar · View at Scopus
  11. M. T. Taghizadeh, Z. Abbasi, and Z. Nasrollahzade, “Study of enzymatic degradation and water absorption of nanocomposites starch/polyvinyl alcohol and sodium montmorillonite clay,” Journal of the Taiwan Institute of Chemical Engineers, vol. 43, no. 1, pp. 120–124, 2012. View at Publisher · View at Google Scholar · View at Scopus
  12. S. D. Yoon, M. H. Park, and H. S. Byun, “Mechanical and water barrier properties of starch/PVA composite films by adding nano-sized poly(methyl methacrylate-co-acrylamide) particles,” Carbohydrate Polymers, vol. 87, no. 1, pp. 676–686, 2012. View at Publisher · View at Google Scholar · View at Scopus
  13. A. B. A. Hariharan and H. P. S. Abdul-Khalil, “Lignocellulose-based hybrid bilayer laminate composite: part I—studies on tensile and impact behavior of oil palm fiber-glass fiber-reinforced epoxy resin,” Journal of Composite Materials, vol. 39, no. 8, pp. 663–684, 2005. View at Publisher · View at Google Scholar · View at Scopus
  14. A. Mandal and D. Chakrabarty, “Isolation of nanocellulose from waste sugarcane bagasse (SCB) and its characterization,” Carbohydrate Polymers, vol. 86, no. 3, pp. 1291–1299, 2011. View at Publisher · View at Google Scholar · View at Scopus
  15. J. I. Morán, V. A. Alvarez, V. P. Cyras, and A. Vázquez, “Extraction of cellulose and preparation of nanocellulose from sisal fibers,” Cellulose, vol. 15, no. 1, pp. 149–159, 2008. View at Publisher · View at Google Scholar · View at Scopus
  16. J. Araki, M. Wada, S. Kuga, and T. Okano, “Flow properties of microcrystalline cellulose suspension prepared by acid treatment of native cellulose,” Colloids and Surfaces A: Physiochemical and Engineering Aspects, vol. 142, no. 1, pp. 75–82, 1998. View at Publisher · View at Google Scholar · View at Scopus
  17. M. J. Cho and B. D. Park, “Tensile and thermal properties of nanocellulose-reinforced poly(vinyl alcohol) nanocomposites,” Journal of Industrial and Engineering Chemistry, vol. 17, no. 1, pp. 36–40, 2011. View at Publisher · View at Google Scholar · View at Scopus
  18. F. Fahma, S. Iwamoto, N. Hori, T. Iwata, and A. Takemura, “Effect of pre-acid-hydrolysis treatment on morphology and properties of cellulose nanowhiskers from coconut husk,” Cellulose, vol. 18, no. 2, pp. 443–450, 2011. View at Publisher · View at Google Scholar · View at Scopus
  19. L. N. Ludueña, A. Vecchio, P. M. Stefani, and V. A. Alvarez, “Extraction of cellulose nanowhiskers from natural fibers and agricultural byproducts,” Fibers and Polymers, vol. 14, no. 7, pp. 1118–1127, 2013. View at Publisher · View at Google Scholar · View at Scopus
  20. J. P. S. Morais, M. F. Rosa, M. M. S. De Souza Filho, L. D. Nascimento, D. M. Do Nascimento, and A. R. Cassales, “Extraction and characterization of nanocellulose structures from raw cotton linter,” Carbohydrate Polymers, vol. 91, no. 1, pp. 229–235, 2013. View at Publisher · View at Google Scholar · View at Scopus
  21. J. F. Revol, H. Bradford, J. Giasson, R. H. Marchessault, and D. G. Gray, “Helicoidal self-ordering of cellulose microfibrils in aqueous suspension,” International Journal of Biological Macromolecules, vol. 14, no. 3, pp. 170–172, 1992. View at Publisher · View at Google Scholar · View at Scopus
  22. S. M. L. Rosa, N. Rehman, M. I. G. De Miranda, S. M. B. Nachtigall, and C. I. D. Bica, “Chlorine-free extraction of cellulose form rice husk and whisker isolation,” Carbohydrate Polymers, vol. 87, no. 2, pp. 1131–1138, 2012. View at Publisher · View at Google Scholar · View at Scopus
  23. W. A. W. A. Rahman, L. T. Sin, A. R. Rahmat, and A. A. Samad, “Thermal behaviour and interactions of cassava starch filled with glycerol plasticized polyvinyl alcohol blends,” Carbohydrate Polymers, vol. 81, no. 4, pp. 805–810, 2010. View at Publisher · View at Google Scholar · View at Scopus
  24. K. Das, D. Ray, N. R. Bandyopadhyay, S. Sahoo, A. K. Mohanty, and M. Misra, “Physico-mechanical properties of the jute micro/nanofibril reinforced starch/polyvinyl alcohol biocomposite films,” Composites Part B: Engineering, vol. 42, no. 3, pp. 376–381, 2011. View at Publisher · View at Google Scholar · View at Scopus
  25. B. M. Cherian, A. L. Leão, S. F. de Souza et al., “Cellulose nanocomposites with nanofibres isolated from pineapple leaf fibers for medical applications,” Carbohydrate Polymers, vol. 86, no. 4, pp. 1790–1798, 2011. View at Publisher · View at Google Scholar · View at Scopus
  26. H. P. S. A. Khalil, H. Ismail, H. D. Rozman, and M. N. Ahmad, “Effect of acetylation on interfacial shear strength between plant fibres and various matrices,” European Polymer Journal, vol. 37, no. 5, pp. 1037–1045, 2001. View at Publisher · View at Google Scholar · View at Scopus
  27. M. Le Troedec, D. Sedan, C. Peyratout et al., “Influence of various chemical treatments on the composition and structure of hemp fibres,” Composites A: Applied Science and Manufacturing, vol. 39, no. 3, pp. 514–522, 2008. View at Publisher · View at Google Scholar · View at Scopus
  28. M. K. Nacos, P. Katapodis, C. Pappas et al., “Kenaf xylan—a source of biologically active acidic oligosaccharides,” Carbohydrate Polymers, vol. 66, no. 1, pp. 126–134, 2006. View at Publisher · View at Google Scholar · View at Scopus
  29. H. Yang, R. Yan, H. Chen, D. H. Lee, and C. Zheng, “Characteristics of hemicellulose, cellulose and lignin pyrolysis,” Fuel, vol. 86, no. 12-13, pp. 1781–1788, 2007. View at Publisher · View at Google Scholar · View at Scopus
  30. A. Alemdar and M. Sain, “Isolation and characterization of nanofibers from agricultural residues—wheat straw and soy hulls,” Bioresource Technology, vol. 99, no. 6, pp. 1664–1671, 2008. View at Publisher · View at Google Scholar · View at Scopus
  31. M. Jonoobi, A. Khazaeian, P. M. Tahir, S. S. Azry, and K. Oksman, “Characteristics of cellulose nanofibers isolated from rubberwood and empty fruit bunches of oil palm using chemo-mechanical process,” Cellulose, vol. 18, no. 4, pp. 1085–1095, 2011. View at Publisher · View at Google Scholar · View at Scopus
  32. E. Abraham, B. Deepa, L. A. Pothan et al., “Extraction of nanocellulose fibrils from lignocellulosic fibres: a novel approach,” Carbohydrate Polymers, vol. 86, no. 4, pp. 1468–1475, 2011. View at Publisher · View at Google Scholar · View at Scopus
  33. F. Fahma, S. Iwamoto, N. Hori, T. Iwata, and A. Takemura, “Isolation, preparation, and characterization of nanofibers from oil palm empty-fruit-bunch (OPEFB),” Cellulose, vol. 17, no. 5, pp. 977–985, 2010. View at Publisher · View at Google Scholar · View at Scopus
  34. A. Dufresne, Nanocellulose: From Nature to High Performance Tailored Materials, Walter de Gruyter, Berlin, Germany, 1st edition, 2012.
  35. R. Li, J. Fei, Y. Cai, Y. Li, J. Feng, and J. Yao, “Cellulose whiskers extracted from mulberry: a novel biomass production,” Carbohydrate Polymers, vol. 76, no. 1, pp. 94–99, 2009. View at Publisher · View at Google Scholar · View at Scopus
  36. A. Bhatnagar and M. Sain, “Processing of cellulose nanofiber-reinforced composites,” Journal of Reinforced Plastics and Composites, vol. 24, no. 12, pp. 1259–1268, 2005. View at Publisher · View at Google Scholar · View at Scopus
  37. D. Klemm, B. Heublein, H. P. Fink, and A. Bohn, “Cellulose: fascinating biopolymer and sustainable raw material,” Angewandte Chemie, vol. 44, no. 22, pp. 3358–3393, 2005. View at Publisher · View at Google Scholar · View at Scopus
  38. M. J. John and R. D. Anandjiwala, “Recent developments in chemical modification and characterization of natural fiber-reinforced composites,” Polymer Composites, vol. 29, no. 2, pp. 187–207, 2008. View at Publisher · View at Google Scholar · View at Scopus
  39. B. Alexandre, D. Langevin, P. Médéric et al., “Water barrier properties of polyamide 12/montmorillonite nanocomposite membranes: structure and volume fraction effects,” Journal of Membrane Science, vol. 328, no. 1-2, pp. 186–204, 2009. View at Publisher · View at Google Scholar · View at Scopus
  40. M. Mucha, S. Ludwiczak, and M. Kawinska, “Kinetics of water sorption by chitosan and its blends with poly(vinyl alcohol),” Carbohydrate Polymers, vol. 62, no. 1, pp. 42–49, 2005. View at Publisher · View at Google Scholar · View at Scopus
  41. S. H. Othman, S. Abdul Rashid, T. I. Mohd Ghazi, and N. Abdullah, “Dispersion and stabilization of photocatalytic TiO2 nanoparticles in aqueous suspension for coatings applications,” Journal of Nanomaterials, vol. 2012, Article ID 718214, 10 pages, 2012. View at Publisher · View at Google Scholar · View at Scopus
  42. M. Roohani, Y. Habibi, N. M. Belgacem, G. Ebrahim, A. N. Karimi, and A. Dufresne, “Cellulose whiskers reinforced polyvinyl alcohol copolymers nanocomposites,” European Polymer Journal, vol. 44, no. 8, pp. 2489–2498, 2008. View at Publisher · View at Google Scholar · View at Scopus
  43. C. Bilbao-Sainz, J. Bras, T. Williams, T. Sénechal, and W. Orts, “HPMC reinforced with different cellulose nano-particles,” Carbohydrate Polymers, vol. 86, no. 4, pp. 1549–1557, 2011. View at Publisher · View at Google Scholar · View at Scopus
  44. W. Chen, H. Yu, and Y. Liu, “Preparation of millimeter-long cellulose I nanofibers with diameters of 30–80 nm from bamboo fibers,” Carbohydrate Polymers, vol. 86, no. 2, pp. 453–461, 2011. View at Publisher · View at Google Scholar · View at Scopus
  45. A. Alhuthali, I. M. Low, and C. Dong, “Characterisation of the water absorption, mechanical and thermal properties of recycled cellulose fibre reinforced vinyl-ester eco-nanocomposites,” Composites Part B: Engineering, vol. 43, no. 7, pp. 2772–2781, 2012. View at Publisher · View at Google Scholar · View at Scopus
  46. W. Zou, J. Peng, Y. Yang, L. Zhang, B. Liao, and F. Xiao, “Effect of nano-SiO2 on the performance of poly(MMA/BA/MAA)/EP,” Materials Letters, vol. 61, no. 3, pp. 725–729, 2007. View at Publisher · View at Google Scholar · View at Scopus