Advances in Polymer Technology

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Volume 2020 |Article ID 7890215 |

Huanlei Yang, Shuxin Zhang, Jinhua Yan, "Chitosan-Reinforced MFC/NFC Aerogel and Antibacterial Property", Advances in Polymer Technology, vol. 2020, Article ID 7890215, 9 pages, 2020.

Chitosan-Reinforced MFC/NFC Aerogel and Antibacterial Property

Academic Editor: Mingzhi Huang
Received31 May 2019
Revised18 Oct 2019
Accepted28 Oct 2019
Published26 Aug 2020


MFC/NFC aerogel has water sensitivity, and it should be improved in strength in water before application. Chitosan was investigated as a MFC/NFC aerogel reinforcing agent in this paper. The reinforced aerogel showed slightly tighter structure and very good water stability and mechanical strength. FTIR disclosed the chemical bonds formed between chitosan and cellulose. Nanoparticles of silver (Ag-NPs) were loaded using the reinforced aerogel. The excellent Ag-NP monodistribution on the aerogel was expressed by TEM. Both chitosan-reinforced Ag-NPs loaded MFC aerogel and NFC aerogel and expressed great antibacterial activity, though reinforced MFC aerogel exhibited better properties, like higher BET, lighter density, more Ag-NP loading, and better distribution, than NFC aerogel in this research. Chitosan-reinforced MFC aerogel is a good potential substrate for nanoparticle loading and biocomposite making.

1. Introduction

Aerogels are porous materials of interconnected nanostructures made from gels by replacing the liquid by gas, which exhibit unusual properties, such as high porosity and surface area, low density, and low heat conductivity [1]. A wide variety of aerogels have been reported in the literature. They can be produced from silica, alumina, tin oxide, chromia, and carbon, with silica being the most widely used one [2]. The unique properties associated with aerogels have led to their use in a wide range of applications such as catalysts [2], catalyst supports [3], superthermal and sound insulators [2, 4], electronics, particle filters, and as a storage media for gases in fuel cells [5, 6]. More recently, cellulose has gained interest as a source material for the production of aerogels due to its renewability and biodegradability [7]. Cellulose aerogels have proven particularly useful in applications where biocompatibility and biodegradability are needed, such as for medicinal, cosmetic, and pharmaceutical applications, opening up the application fields of aerogels even wider [8]. Micro/nanofibrillar cellulose (MFC/NFC) is isolated from natural cellulose fibers by basically mechanical action after enzyme or chemical pretreatment. Its higher aspect ratio made MFC/NFC an attractive application of providing a more beneficial template to accommodate nanoparticles, for example, NFC with silver nanoparticles using UV reduction [9], NFC with magnetic particles [10], and NFC with drug nanoparticles [11].

MFC/NFC aerogels generally can be prepared by two steps: one is the MFC/NFC suspension generated by a unique method of enzymatic/chemical pretreatment and mechanical fibrillation by a microfluidizer and the other is to produce aerogel by freezing the suspensions and dried in a special way [7, 1215]. Different cellulose sources and preparation processes make the MFC/NFC cellulose aerogels with totally different microstructures and properties [16, 17]. MFC/NFC has been widely investigated recently due to its sustainable, renewable, and biocompatible nontoxic properties for relatively high physical-chemical stability materials [18, 19]. The density and surface texture of the aerogels can be tuned by selecting the concentration of the MFC/NFC dispersion before freeze-drying. All of these aerogels are based on the hydrogen bond formation between MFC/NFCs [20]. Unfortunately, these hydrogen bonds can be easily destroyed by immersing the aerogels in water, which limited the application of the aerogels [20].

Chemical cross-linking affords a method for the preparation of MFC/NFC cellulose aerogels with high mechanical properties [2123]. Although these efforts have been carried out for the improvement of the mechanical properties of cellulose aerogels, the substances that can provide safe, renewable, and biocompatible nontoxic properties are more desirable. Chitosan from the natural polymer chitin has good biocompatibility, as well as extensive applications in pharmacology, biomedicine, agriculture, food, and waste treatment [24]. Regarding the chemical nature, chitosan and cellulose have similar structures, with the same β-glycosidic linkages, being the main difference as the presence of primary amino groups at most of the C-2 positions in chitasan, instead of the hydroxyl groups. Much work has been devoted to the study of chitosan blends with cellulose [2528], poly(vinyl alcohol) [2931], gelatin [32], collagen [33], and others [34]. The evidence of some chitosan–cellulose chemical interactions was proved [19]. Our group also reported that chitosan improved the nanopaper mechanical strength both in dry and wet states by cross-linking [35]. That is, chitosan can be used as a cross-linker of cellulose and nanofibrils.

In the current work, we firstly reported chitosan-reinforced MFC/NFC aerogels and their application. The aerogels showed improved mechanical properties. Using the reinforced aerogel as a template, nanoparticles, silver as an example, were loaded uniformly.

2. Materials and Methods

2.1. MFC/NFC Preparation

Fully bleached eucalyptus pulp was passed through the microgrinder, 6 passes, at a concentration of 2.31%, to produce MFC suspension. Then some of the MFC suspension was treated by TEMPO before passing the microfluidizer 10 times to produce NFC. The TEMPO oxidation technique was performed as given in the literature with sodium hypochlorite as the terminal oxidant [36]. Dialysis was applied to remove extra salts in NFC using Nomial MWCO 3500 (Fisherbrand regenerated cellulose) for 48 h with Milli-Q water changing frequency every 5 h. The acidic group content of MFC and NFC was measured as 70 and 400 μmol/g, respectively, by titration as per the literature [37]. The titration steps were as follows: 0.01 M NaOH was added drop by drop till there was no further drop in system conductivity. Then the amount of NaOH was recorded till the conductivity increased. The consumed NaOH can be calculated to get the acidic group content. Both MFC and NFC ready-to-use slurries were kept in a refridgerator.

2.2. Chitosan Solution Preparation

Chitosan (MW 10253, viscosity 20 cP) was purchased from Aldrich (degree of deacetylation: ∼85%). Chitosan solutions were prepared by dissolving chitosan (2% by weight) in (1% by volume) aqueous acetic acid solution [38]. The solution was sonicated for 30 min before use.

2.3. MFC/NFC Aerogel Preparation

MFC/NFC dispersion with chitosan mixture at different ratios of 100/0, 90/10, 80/20, and 70/30 (MFC to chitosan weight) was mixed to 0.5% by adding DI water, by using a high-shear mixer for 5 min, followed by a magnetic bar stirring for 1 h, and then sonication for another 30 min. Then the mixture was centrifuged to remove water at a speed of 1.2 × 104 rpm for 1 h. A gel was formed. The gel was frozen by liquid nitrogen, then placed on a freeze dryer (Labconco) for at least 48 h. The properties of density, strength, and BET surface area were examined. The density was measured by the volume and weight of each aerogel. The strength was evaluated by its water stability which was conducted in water for stirring at a given time. After Ag-NPs loaded, both the MFC/CH aerogel and NFC/CH aerogel BET surface areas were measured after 4 h degassing at 105°C (Gemini VII Series surface area analyzer, Micromeritics Instrument Corporation).

2.4. Nanoparticle Loading

The in situ loading of silver nanoparticles (Ag-NPs) onto the aerogels was carried out through the reduction of 10 mM AgNO3 solution. Under ambient temperature (∼25°C), AgNO3 solution was absorbed by the porous matrix by soaking or dropwise addition, keeping totally wet for enough time till the aerogels are not absorbing solution anymore. After a certain time of air drying, a partially dehydrated matrix was obtained. It was then immersed in an aqueous solution of NaBH4 (50 mM) for 20 min. The color of the samples turned to yellow or dark brown due to the reduction of Ag + into silver nanoparticles. The composite was rinsed with Milli-Q water three times to remove water-soluble substances and unbound silver particles. Finally, the composite was freeze dried.

2.5. Aerogel Morphology

SEM sample preparation of the MFC/NFC slurry and aerogels with/without Ag-NPs : MFC/NFC (20 mL, 0.08%) was taken for magnetic stirring for 45 min, followed by 30 s sonication. A silicon plate was used as the MFC/NFC material support. Firstly, the plate was cut into small pieces, which were soaked in 10% NaOH solution for 30 s and then in Milli-Q water. These silicon pieces were dried by nitrogen blowing, followed by UV exposure for 20 min. A tiny drop of the abovementioned MFC/NFC slurry was placed on the surface of a cleaned silicon piece. Overnight air drying was needed before the SEM test. The samples were coated with gold before SEM operation. The porous structures of MFC/NFC aerogels were examined using a field emission scanning electron microscope (FESEM) at an accelerating voltage of 20 kV (a high resolution JEOL 6400F cold field emission SEM). The MFC/NFC aerogels with Ag-NPs were characterized using VPSEM (Variable Pressure Scanning Electron Microscope, Hitachi S3200N) with an energy dispersive X-ray spectrometer).

TEM preparation of MFC/NFC aerogels with Ag-NPs: A JEOL 2000FX transmission electron microscope (TEM) operating at 20.0 kV was utilized to define the Ag-NPs in the MFC/NFC aerogels. A specimen can be prepared by cutting the sample into thin slices using a diamond saw, then cutting 3-mm-diameter disks from the slice, thinning the disk on a grinding wheel, dimpling the thinned disk, and then ion milling it to electron transparency.

2.6. FTIR Spectroscopy

FTIR spectroscopy was performed on a PerkinElmer Spectrum (Version 10.03.09). Spectra were obtained after the accumulation of 6 scans which had a resolution of 4 cm−1 over the range of 4,000–650 cm−1.

2.7. Thermal Gravimetric Analysis (TGA)

In order to determine the thermal decomposition temperature of composite aerogels, thermogravimetric analysis (TGA) was used. It was operated on Perkin Elmer TGA Q500 with a heating rate of 10°C/min to 500°C in a nitrogen atmosphere. In order to obtain the amount of Ag-NPs in aerogel, TGA under oxygen in the range of 500–575°C was continued. The isothermal time for 25 min at 575°C was utilized.

2.8. Antibacterial Activity Test

The antibacterial activity of the aerogels was tested against Escherichia coli (E. coli), Gram-negative bacteria, using the viable cell-counting method. Briefly, about 100 μL E. coli was cultivated in 100 mL of a nutrient broth solution to give a bacterial concentration of about 7 × 1011 CFU/mL. Then, 1 mL of the bacteria/nutrient solution was added to 9 mL of sterilized nutrient broth solution (0.8%). Several decimal dilutions were performed until the bacterial concentration increased from 7 × 103 to 7 × 107 CFU/mL. NFC, NFC/chitosan, and MFC/chitosan and their silver-loaded counterparts (NFC/chitosan/Ag-NPs and MFC/chitosan/Ag-NPs) were used in the antibacterial tests. Accurate weight of the aerogel samples (100 mg) was assigned to the experiment. To perform the antibacterial testing, aerogels of the respective samples were put into 10 mL of the bacteria/nutrient solution and incubated in a shaker at 37°C for 12 h. After the exposure of the bacteria to films, 100 μL of the bacterial solution was taken out and quickly spread on a plate containing nutrient agar. Plates containing bacteria were incubated at 37°C for 24 h, and then the numbers of the surviving colonies were observed. These results were compared to the number of bacterial colonies of the untreated control.

3. Results and Discussion

3.1. MFC/NFC Aerogel Physical Properties

MFC/NFC aerogels with chitosan addition were examined for their densities and strength. The dry aerogel-retained stability in water is shown in Figure 1. MFC aerogels with 0% chitosan (A), 10% chitosan (B), and 20% chitosan (C) were soaked into water and kept under magnetic stirring at 610 rpm for 4 h. MFC aerogel with 0% chitosan was totally dispersed into water again, chitosan-added MFC aerogels were kept intact. In addition, a 10% chitosan-added MFC aerogel compression test was conducted for mechanical strength property of 0.36 MPa. The dry aerogel density was tested by measuring the volume of the aerogel and its weight. Table 1 is the density calculation data of the produced aerogels under 2% concentration, which is in accordance with that of cellulose-based chitosan aerogel [25]. The data showed that, with increase in chitosan level, the aerogel density rose. It implied that chitosan can shrink the aerogel pores and tighten the MFC/NFC aerogel structure.

Aerogel density (g/cm3)CH0%CH10%CH20%CH30%


Note: pure MFC aerogel densities were obtained with 0.0258, 0.0505, and 0.0807 g/cm3 from 2%, 5%, and 8% MFC gel concentrations, respectively.

After Ag-NPs loaded, both MFC/CH aerogel and NFC/CH aerogel surface areas were measured after 4 h degassing at 105°C. The results are listed in Table 2. In Table 2, NFC/CH aerogel has lower BET data than MFC/CH after Ag loaded. Due oxidation, the NFC possessed the acidic group content up to 400 μmol/g, while MFC possessed the acidic group content of 70 μmol/g. As a result, NFC was more active with chitosan and formed a tighter aerogel structure [25]. Accordingly, its BET is smaller than that of MFC/CH aerogel. The higher BET data also imply that the aerogel has more space exposure to which gives pores benefit particles/solution filling. As a result, we found that the MFC/CH aerogel loaded more nanoparticles than the NFC/CH aerogel (see Table 3).

Aerogel BET m2/gCH10% Ag loadedCH20% Ag loadedCH30% Ag loadedCH0% Ag loadedCH30% with no Ag


Ag-NPs %CH 0%CH 10%CH 20%CH 30%

MFC aerogel2.
NFC aerogel3.233

3.2. MFC/NFC Aerogel Microscopy

MFC/NFC aerogels with different chitosan addition levels were conducted and scanned using a SEM. Generally, chitosan can cause the aerogel dense structure with the increase in addition level (see Figure 1). The structural change is clear also in these SEM images. When MFC aerogel contains 0% chitosan, its structure is open and the pores are easily seen (Figure 1(a)). When a small amount of chitosan solution added (Figure 1(b)), we can see the light “films” formed among pores like fogs. With increasing chitosan content to 20% (Figure 1(c)), these light “films” became thicker. After 30% chitosan added (Figure 1(d)), these films were so dense that the aerogel structure had less existing pores. This is because of the characteristic properties of chitosan, natively containing the high content of primary amino groups. Cellulose with several compounds which having primary amino groups, such as polyethylenimines, ethylenediamine, and benzyl amine, revealed the formation of new chemical bonds in the materials processed even at room temperature [20]. Here aerogel making employed the main reaction between amino and carbonyl groups, besides hydrogen bonds of cellulose and chitosan groups, to improve its mechanical strength [20, 25]. Since NFC has much more exposed carboxyl/carbonyl groups than MFC, theoretically NFC/CH aerogel would result in more reaction between NFC and chitosan. In Figure 1, we did observe the tighter structure of NFC/CH aerogels (pictures E, F, and G in Figure 1) than that of MFC/CH (pictures A, B, C, and D in Figure 1). Fewer pores but more “films” were formed in NFC/CH aerogel. The data presented in Tables 13 are additional evidences to confirm this observation.

After Ag-NPs loaded, these aerogels exhibited similar SEM morphology to that of Ag-NPs unloaded, in which structures are denser with the increase in chitosan. This denser structure caused the nanoparticles to fill differently. Denser aerogel has relatively tight structure and fewer capillaries, which penetrates less Ag+ and reducing solution, resulting in fewer Ag-NPs generated. Table 3 shows the amount of Ag-NPs in MFC/NFC aerogels after 575°C oxygen for 25 min isothermal time under TGA. It disclosed that NFC aerogel has loaded fewer Ag-NPs than MFC aerogels.

In order to investigate how the nanoparticles are located in these aerogels, the MFC/CH and NFC/CH aerogels with Ag-NPs were scanned by using SEM in high magnification. The images are shown in Figure 2. Since nanoparticles are expected to locate evenly in smaller size on the composite, any aggregates should be avoided. All NFC aerogels showed particle aggregates (pictures D, E, and Figure 2), but only MFC-30% CH aerogel showed Ag-NP aggregates (picture C in Figure 2). The formation of Ag-NP aggregates may be from the rich hydroxyl and carboxyl groups which absorb much Ag+ solution. But there are less free hydroxyl and carboxyl groups in denser aerogel after drying. While ‘films’ are formed, the Ag+ concentrate was forced to sit in pores and then enwrapped as aggregates. These free groups present negative charge, providing the anchor sites for Ag + uniformly in loose aerogels of MFC/CH with 10% and 20% chitosan. They are better aerogels for nanoparticle loading.

Ag-NP size and distribution for aerogel are very important. Based on good particle distribution in SEM images shown in Figure 2, MFC aerogel with 20% CH was chosen and TEM observation was conducted (see Figure 3). From the TEM image, we can see that the particles are monodispersed and have very small size. Using ImageJ software, the TEM image shown in Figure 3(a) was analyzed for particle size distribution automatically with every size scale bar (0.72 nm) starting at 4.13 nm. Most particles are in the range of 4–9 nm with a mean diameter of 7.08 nm. This is because the aerogel was treated by very dilute AgNO3 solution (10 mM) and there were less Ag + surrounding nanofibrils, typically at negative charged groups, which are the anchors to be the nucleus of particle growth. Nanofibrils played an important role to physically stop the Ag + free movement, and then monodispersed small particles were formed. With more chitosan in aerogels, since chitosan amino groups consumed some carbonyl groups on MFC/NFC, and most possibly chitosan molecules have strong hydrogen bonds with MFC/NFC (it is to observe “films” in SEM images), and these aerogels lost many uniform places to accommodate Ag+, resulting in particle aggregates, as we can see in C, D, E, and F of Figure 2.

3.3. FTIR Spectroscopy

The spectra of MFC aerogel with 20% chitosan is shown in Figure 4, along with MFC aerogel blank and NFC/CH areogel (marked as B, A, and C respectively, in Figure 4). The peaks at 3330–3340 cm−1 corresponded to the stretching vibration of hydroxyl groups. These peak intensities reinforced for MFC/NFC aerogel blended chitosan due to the N–H groups involvment [39]. The main change observed in the spectra is no sharp peaks at 1650 cm−1 which corresponded to the carbonyl stretch and 1560 cm−1 to the amino groups of chitosan in B and C of Figure 4, implying the chemical reaction between chitosan and cellulose [20]. This also explained why we observed the aerogel tight structure with chitosan under SEM.

3.4. Thermal Gravimetric Analysis (TGA)

In view of the importance of thermal stability in many applications of MFC/NFC aerogels, we examined thermal decomposition of composite-loaded Ag-NPs by thermogravimetry (TGA, Perkin Elmer Q500, and heating rate of 10°C/min) in a nitrogen atmosphere under 500°C, as shown in Figure 5. In all TGA curves, the small weight losses below 150°C apparently resulted from evaporation of adsorbed moisture. Under nitrogen, the decomposition behavior of the MFC-Ag aerogel was nearly the same with different levels of chitosan, the most weight loss taking place at 280°C; meanwhile, NFC-Ag aerogels have lower decomposition temperature of around 250°C. Chitosan did not change both MFC and NFC aerogel thermal stability. In order to obtain the Ag-NP amount in aerogel, TGA under oxygen in the range of 500–575°C was continued. The isothermal time for 25 min at 575°C was set up. The results are listed in Table 3. The Ag-NPs in MFC/CH aerogel has slightly higher amount than that in NFC/CH aerogel, but the former has more uniform particle distribution.

3.5. Antibacterial Activity Testing

The antibacterial activity of these four samples MFC80/CH20, NFC80/CH20, MFC80/CH20/Ag-NPs, and NFC80/CH20/Ag-NPs was tested against E. coli by using the viable cell-counting method. NFC aerogel without chitosan was compared. The effects of aerogels on the growth of the recombinant bacteria E. coli are shown in Figure 6. “Blank” in Figure 6 means a plate which was produced from untreated bacterial solution. As shown in the plates, no bacterial colonies were observed at concentrations of 7 × 107 CFU/mL for both MFC/CH-Ag-NPs and NFC/CH-Ag-NPs which represent the highest antibacterial activity. On the other hand, many bacterial colonies were observed for MFC-CH, NFC-CH, and NFC aerogels which implied poor antibacterial activity. Though chitosan is considered as a good natural polymer for medical application due to its antibacterial property, Ag-NPs in these aerogels imported much better inhibition of bacteria than chitosan. MFC/CH-Ag-NPs may have better antibacterial property than NFC/CH-Ag-NPs since the former has excellent nanoparticle distribution. This should be further examined.

4. Conclusions

In the current work, we successfully utilized chitosan as MFC/NFC aerogel reinforcement biopolymer. The reinforced aerogels have overcome the water unstability. With more chitosan addition, MFC/NFC aerogels became denser which have tighter structures that are observed in SEM. Chemical reaction occured between chitosan and MFC/NFC. Comparing both MFC/CH and NFC/CH aerogels, MFC/CH aerogel has higher BET surface area and lower density than NFC/CH aerogel. Ag-NPs were in site loaded to chitosan-added MFC/NFC aerogel. The MFC/CH aerogel performed much better than the NFC/CH aerogel, which obtained monodispersed nanoparticles of Ag-NPs. Finally, both MFC/CH-Ag-NP and NFC/CH-Ag-NP aerogels exhibited excellent antibacterial activity. But the better antibacterial performance of both aerogels should be further examined.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare no conflicts of interest.


The authors would like to thank Prof. Orlando J. Rojas and his group for their help during this research and in editing the manuscript. The Special Support Plan for Xijiang Innovation Team Plan 2016, High-Level Talent Cultivation of Guangdong Industry Polytechnic (No. KYRC2018-020), and Guangdong University Youth Innovation Fund Project (No. 2018GKQNCX032) are greatly acknowledged for the support.

Supplementary Materials

The SEM images showing the surface of MFC aerogel with 10% chitosan addition and 20% chitosan addition. (Supplementary Materials)


  1. A. C. Pierre and G. M. Pajonk, “Chemistry of aerogels and their applications,” Chemical Reviews, vol. 102, no. 11, pp. 4243–4266, 2002. View at: Publisher Site | Google Scholar
  2. U. Schubert, “Silica-based and transition metal-based inorganic-organic hybrid materials—a comparison,” Journal of Sol-Gel Science and Technology, vol. 26, no. 1–3, pp. 47–55, 2003. View at: Google Scholar
  3. E. Guilminot, F. Fischer, M. Chatenet et al., “Use of cellulose-based carbon aerogels as catalyst support for PEM fuel cell electrodes: electrochemical characterization,” Journal of Power Sources, vol. 166, no. 1, pp. 104–111, 2007. View at: Publisher Site | Google Scholar
  4. R. Baetens, B. P. Jelle, and A. Gustavsen, “Aerogel insulation for building applications: a state-of-the-art review,” Energy and Buildings, vol. 43, no. 4, pp. 761–769, 2011. View at: Publisher Site | Google Scholar
  5. J. Biener, M. Stadermann, M. Suss et al., “Advanced carbon aerogels for energy applications,” Energy & Environmental Science, vol. 4, no. 3, pp. 656–667, 2011. View at: Publisher Site | Google Scholar
  6. G. Nyström, A. Marais, E. Karabulut, L. Wågberg, Yi Cui, and M. M. Mahiar, “Self-assembled three-dimensional and compressible interdigitated thin-film supercapacitors and batteries,” Nature Communications, vol. 6, no. 1, p. 7259, 2015. View at: Publisher Site | Google Scholar
  7. R. Gavillon and T. Budtova, “Aerocellulose: new highly porous cellulose prepared from cellulose−NaOH aqueous solutions,” Biomacromolecules, vol. 9, no. 1, pp. 269–277, 2008. View at: Publisher Site | Google Scholar
  8. S. R. Ma, Q. Mi, J. Yu, J. He, and J. Zhang, “Aerogel materials based on cellulose,” Progress in Chemistry, vol. 26, no. 5, pp. 796–809, 2014. View at: Google Scholar
  9. H. Dong, J. F. Snyder, D. T. Tran, and J. L. Leadore, “Hydrogel, aerogel and film of cellulose nanofibrils functionalized with silver nanoparticles,” Carbohydrate Polymers, vol. 95, no. 2, pp. 760–767, 2013. View at: Publisher Site | Google Scholar
  10. T. Nypelö, H. Pynnönen, M. Österberg, J. J. Paltakari, and J. Laine, “Interactions between inorganic nanoparticles and cellulose nanofibrils,” Cellulose, vol. 19, no. 3, pp. 779–792, 2012. View at: Publisher Site | Google Scholar
  11. H. Valo, S. Arola, P. Laaksonen et al., “Drug release from nanoparticles embedded in four different nanofibrillar cellulose aerogels,” European Journal of Pharmaceutical Sciences, vol. 50, no. 1, pp. 69–77, 2013. View at: Publisher Site | Google Scholar
  12. K. J. De France, T. Hoare, and E. D. Cranston, “Review of hydrogels and aerogels containing nanocellulose,” Chemistry of Materials, vol. 29, no. 11, pp. 4609–4631, 2017. View at: Publisher Site | Google Scholar
  13. J. T. Korhonen, M. Kettunen, R. H. A. Ras, and O. Ikkala, “Hydrophobic nanocellulose aerogels as floating, sustainable, reusable, and recyclable oil absorbents,” ACS Applied Materials & Interfaces, vol. 3, no. 6, pp. 1813–1816, 2011. View at: Publisher Site | Google Scholar
  14. R. Sescousse, A. Smacchia, and T. Budtova, “Influence of lignin on cellulose-NaOH-water mixtures properties and on aerocellulose morphology,” Cellulose, vol. 17, no. 6, pp. 1137–1146, 2010. View at: Publisher Site | Google Scholar
  15. R. Sescousse, R. Gavillon, and T. Budtova, “Aerocellulose from cellulose-ionic liquid solutions: preparation, properties and comparison with cellulose-NaOH and cellulose-NMMO routes,” Carbohydrate Polymers, vol. 83, no. 4, pp. 1766–1774, 2011. View at: Publisher Site | Google Scholar
  16. C. Aulin, J. Netrval, L. Wågberg, and T. Lindström, “Aerogels from nanofibrillated cellulose with tunable oleophobicity,” Soft Matter, vol. 6, no. 14, pp. 3298–3305, 2010. View at: Publisher Site | Google Scholar
  17. H. Sehaqui, M. Salajková, Q. Zhou, and L. A. Berglund, “Mechanical performance tailoring of tough ultra-high porosity foams prepared from cellulose I nanofiber suspensions,” Soft Matter, vol. 6, no. 8, pp. 1824–1832, 2010. View at: Publisher Site | Google Scholar
  18. R. J. Moon, A. Martini, J. Nairn, J. Simonsen, and J. Youngblood, “Cellulose nanomaterials review: structure, properties and nanocomposites,” Chemical Society Reviews, vol. 40, no. 7, pp. 3941–3994, 2011. View at: Publisher Site | Google Scholar
  19. J. M. Urreaga and M. U. de la Orden, “Chemical interactions and yellowing in chitosan-treated cellulose,” European Polymer Journal, vol. 42, no. 10, pp. 2606–2616, 2006. View at: Publisher Site | Google Scholar
  20. W. Zhang, Y. Zhang, C. Lu, and Y. Deng, “Aerogels from crosslinked cellulose nano/micro-fibrils and their fast shape recovery property in water,” Journal of Materials Chemistry, vol. 22, no. 23, pp. 11642–11650, 2012. View at: Publisher Site | Google Scholar
  21. L. Guo, Z. Chen, S. Lyu, F. Fu, and S. Wang, “Highly flexible cross-linked cellulose nanofibril sponge-like aerogels with improved mechanical property and enhanced flame retardancy,” Carbohydrate Polymers, vol. 179, pp. 333–340, 2018. View at: Publisher Site | Google Scholar
  22. A. Kumar, Y. Lee, D. Kim et al., “Effect of crosslinking functionality on microstructure, mechanical properties, and in vitro cytocompatibility of cellulose nanocrystals reinforced poly (vinyl alcohol)/sodium alginate hybrid scaffolds,” International Journal of Biological Macromolecules, vol. 95, pp. 962–973, 2017. View at: Publisher Site | Google Scholar
  23. T. Nissilä, S. S. Karhula, S. Saarakkala, and K. Oksman, “Cellulose nanofiber aerogels impregnated with bio-based epoxy using vacuum infusion: structure, orientation and mechanical properties,” Composites Science and Technology, vol. 155, pp. 64–71, 2018. View at: Publisher Site | Google Scholar
  24. G. Skjak-Brack, T. Anthonsen, P. Sandford et al., Chitin and Chitosan: Sources Chemistry, Biochemistry, Physical Properties, and Applications, Elsevier Applied Science, London, UK, 1989.
  25. Z. Li, L. Shao, W. Hu et al., “Excellent reusable chitosan/cellulose aerogel as an oil and organic solvent absorbent,” Carbohydrate Polymers, vol. 191, pp. 183–190, 2018. View at: Publisher Site | Google Scholar
  26. H. Yang, A. Sheikhi, and T. G. M. van de Ven, “Reusable green aerogels from cross-linked hairy nanocrystalline cellulose and modified chitosan for dye removal,” Langmuir, vol. 32, no. 45, pp. 11771–11779, 2016. View at: Publisher Site | Google Scholar
  27. G. Meng, H. Peng, J. Wu et al., “Fabrication of superhydrophobic cellulose/chitosan composite aerogel for oil/water separation,” Fibers and Polymers, vol. 18, no. 4, pp. 706–712, 2017. View at: Publisher Site | Google Scholar
  28. Z. Liu, H. Wang, C. Liu et al., “Magnetic cellulose-chitosan hydrogels prepared from ionic liquids as reusable adsorbent for removal of heavy metal ions,” Chemical Communications, vol. 48, no. 59, pp. 7350–7352, 2012. View at: Publisher Site | Google Scholar
  29. T. Zhai, Q. Zheng, Z. Cai, L.-S. Turng, H. Xia, and S. Gong, “Poly (vinyl alcohol)/cellulose nanofibril hybrid aerogels with an aligned microtubular porous structure and their composites with polydimethylsiloxane,” ACS Applied Materials & Interfaces, vol. 7, no. 13, pp. 7436–7444, 2015. View at: Publisher Site | Google Scholar
  30. L. Wei, Q. Wu, Z Xin et al., “Enhanced thermal and mechanical properties of PVA composites formed with filamentous nanocellulose fibrils,” Carbohydrate Polymers, vol. 113, pp. 403–410, 2014. View at: Publisher Site | Google Scholar
  31. Q. Zheng, Z. Cai, and S. Gong, “Green synthesis of polyvinyl alcohol (PVA)-cellulose nanofibril (CNF) hybrid aerogels and their use as superabsorbents,” Journal of Materials Chemistry A, vol. 2, no. 9, pp. 3110–3118, 2014. View at: Publisher Site | Google Scholar
  32. I. S. Arvanitoyannis, A. Nakayama, and S.-I. Aiba, “Chitosan and gelatin based edible films: state diagrams, mechanical and permeation properties,” Carbohydrate Polymers, vol. 37, no. 4, pp. 371–382, 1998. View at: Publisher Site | Google Scholar
  33. A. Sionkowska, M. Wisniewski, J. Skopinska, C. J. Kennedy, and T. J. Wess, “Molecular interactions in collagen and chitosan blends,” Biomaterials, vol. 25, no. 5, pp. 795–801, 2004. View at: Publisher Site | Google Scholar
  34. Y. Zhou, S. Fu, L. Zhang, H. Zhan, and M. V. Levit, “Use of carboxylated cellulose nanofibrils-filled magnetic chitosan hydrogel beads as adsorbents for Pb(II),” Carbohydrate Polymers, vol. 101, pp. 75–82, 2014. View at: Publisher Site | Google Scholar
  35. M. S. Toivonen, S. Kurki-Suonio, F. H. Schacher, S. Rojas, O. J. Rojas, and O. Ikkala, “Water-resistant, transparent hybrid nanopaper by physical cross-linking with chitosan,” Biomacromolecules, vol. 16, no. 3, pp. 1062–1071, 2015. View at: Publisher Site | Google Scholar
  36. T. Saito, S. Kimura, Y. Nishiyama, and A. Isogai, “Cellulose nanofibers prepared by TEMPO-mediated oxidation of native cellulose,” Biomacromolecules, vol. 8, no. 8, pp. 2485–2491, 2007. View at: Publisher Site | Google Scholar
  37. A. E. Horvath and T. Lindström, “Indirect polyelectrolyte titration of cellulosic fibers—surface and bulk charges of cellulosic fibers,” Nordic Pulp & Paper Research Journal, vol. 22, no. 1, pp. 87–92, 2007. View at: Publisher Site | Google Scholar
  38. S. C. M. Fernandes, L. Oliveira, C. S. R. Freire et al., “Novel transparent nanocomposite films based on chitosan and bacterial cellulose,” Green Chemistry, vol. 11, no. 12, pp. 2023–2029, 2009. View at: Publisher Site | Google Scholar
  39. S. Peng, Y. Liu, Z. Xue et al., “Modified nanoporous magnetic cellulose-chitosan microspheres for efficient removal of Pb(II) and methylene blue from aqueous solution,” Cellulose, vol. 24, no. 11, pp. 4793–4806, 2017. View at: Publisher Site | Google Scholar

Copyright © 2020 Huanlei Yang 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.

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