UV-absorbing cellulose nanocrystals as functional reinforcing ﬁ llers in polymer nanocomposite ﬁ lms

a Reinforcing, surface-functionalized cellulose nanocrystals (CNCs) with photoactive groups were obtained from wood cellulose ﬁ bers using sequential periodate oxidation and a “ click-type ” reaction between aldehyde groups and p -aminobenzoic acid in an aqueous environment, followed by mechanical disintegration. In the solution state, CNCs exhibited very high UV-absorption properties, especially in UVA and UVB regions (100% absorption was achieved with only 0.1% of CNCs) and high transparency in the visible light region (around 90% with 0.1% of CNCs). The fabricated CNCs functioned as lightweight-reinforcing ﬁ llers with high UV-absorption capability when incorporated into a poly(vinyl alcohol) (PVA) matrix. Complete UVA and UVB opacity of the nanocomposite was achieved using 10% of CNCs while simultaneously retaining over 80% transparency over the whole visible light spectrum. In addition, up to 33% and 77% higher tensile strength and modulus, respectively, were achieved using 10% of CNCs compared to pristine PVA. This result presented a unique way to produce multifunctional CNCs to be incorporated into nanocomposite structures instead of metal nanoparticles. These CNCs are supposed to be suitable for many applications requiring high visible light transparency and blocking of UV radiation.


Introduction
The addition of functional llers can signicantly improve the properties of organic transparent polymers, as they confer new features on the materials, including magnetoelasticity, 1 a high reectance index, and absorption of specic wavelengths of light (e.g., UV). 2 UV-absorption properties are important in many applications, as although the energy of UV light is too low to cause ionization, it can accelerate many chemical reactions, causing severe damage to animals, plants, 3 and materials. 4In particular longer wavelength UVB (280-315 nm) and UVA (315-400 nm) are important from a biological perspective, as they are not or only partially adsorbed by the ozone layer, whereas shorter wavelength UVC (100-280 nm) is completely eliminated at the stratosphere. 5To prevent UV light induced damage, highly transparent UV-absorption materials are required, for example, in health science, such as in ophthalmology. 6The high transparency of a polymer matrix can be retained by using nanoscale-sized llers, which do not absorb and scatter visible light.Most functional llers are composed of inorganic nanoparticles, such as ZnO or TiO 2 . 1 Although inorganic nanoparticles that block UV light have several advantages, including a long life cycle, there are health and environmental concerns surrounding their use.8][9] Inorganic nanoparticles may also induce photodegradation of polymers. 10In addition, some inorganic nanoparticles are produced using costly metals, which decrease their economic and ecological viability.
Nanocellulose, which can be isolated from numerous cellulosic sources, is a relatively novel class of biomaterials. 11Long cellulose nanobers (CNFs) are mostly obtained by mechanical disintegration of natural or chemically modied cellulose bers. 12Short and rod-like cellulose nanocrystals (CNCs) are produced by acid hydrolysis of amorphous parts of cellulose. 13][16][17] Both CNFs and CNCs are promising materials for many highend applications, as they are lightweight, biodegradable, have a large surface area, and are produced from cellulose, which is a renewable and abundant biopolymer. 18They are also relatively nontoxic, although their toxicity depends on the production method (i.e., the chemistry applied during the preparation). 19ue to the lightweight and high strength of CNFs and CNCs, they have been studied as organic ller materials for synthetic and natural nanocomposites. 20So far most of the research has concentrated on improving the mechanical properties of nanocomposites by exploiting the high reinforcing effect of nanocellulose.However, the potential of nanocellulose as a bifunctional UV-absorbing and reinforcing ller in composites has not been widely reported.UV-absorbing nanocomposites containing CNCs with lignin 21 and CNFs with ZnO nanoparticles 22 have been produced, but their UV absorption was based on the presence of lignin or ZnO nanoparticles.
Postchemical polymerization of CNCs with polyrhodanine was shown to alter visible light absorption properties of CNCs depending on the pH and polyrhodanine-functionalized CNCs were proposed as pH indicators. 23A CNF aerogel with photoswitchable water absorption properties was studied, but the photoactive properties of the gel were due to a TiO 2 coating. 24erein, we report the fabrication of photoactive CNCs based on a "click-type" reaction between p-aminobenzoic acid (PABA) and periodate-oxidized cellulose.CNCs were then used in nanocomposite lms together with poly(vinyl alcohol) (PVA) as the polymer matrix.The aim of the study was to investigate the properties of CNCs produced by this method and their use as a UV absorbing reinforcement agent for PVA.In particular, the effect of the amount of CNCs (0-10%) on the properties of PVA was investigated.

Materials
Bleached birch pulp (Betula pendula) was obtained as dry sheets and used as a cellulose material aer disintegration in deionized water.The p.a. grade chemicals used for the periodate oxidation (NaIO 4 ), the aldehyde content analyses (NH 2 OH$HCl) and the fabrication of nanocomposite lms (PVA (Mowiol 3-96, 96.8-97.6 mol% hydrolysis)) were obtained from Sigma-Aldrich (Germany).p-Aminobenzoic acid was obtained from TCI (Germany).All the chemicals were used as received, without further purication.Deionized water was used throughout the experiments.

Synthesis and fabrication of p-aminobenzoic acid modied cellulose nanocrystals
The pulp sample was oxidized with sodium metaperiodate by weighing 12.0 g (dry weight) of cellulose in a 2000 ml ask and adding 1200 ml of deionized water and 9.84 g of NaIO 4 .The reaction vessel was covered with aluminum foil to prevent photoinduced decomposition of periodate, and the mixture was stirred with a magnetic stirrer in a water bath at 75 C, together with 21.6 g of LiCl as an additive.Aer 3 h, the product was ltered and washed several times with deionized water to remove iodine-containing compounds.Undried periodateoxidized pulp was then allowed to react with sodium 4-aminobenzoate (10 times molar excess compared to the aldehyde groups) for 72 h at pH 5.8 using dilute HCl solution.Aer the reaction, the product was ltered and washed with deionized water.The washed pulp was diluted to 2% with water, and the pH was adjusted to 7 by adding a few drops of dilute NaOH solution, followed by further dilution to 1% using water.The sample was then disintegrated using a microuidizer (Micro-uidics M-110EH-30), with one pass through 400 and 200 mm chambers at a pressure of 1300 bar, then passed once through 400 and 100 mm chambers at a pressure of 2000 bar, and nally passed once through 200 and 87 mm chambers at a pressure of 2000 bar.Reference CNCs with carboxylic acids were prepared according to the reported methodologies based on our previous study. 25tical transmittance of cellulose nanocrystal solutions Diluted solutions (0.1-0.5%) were prepared using water and UV-Vis spectra (190-800 nm) were recorded with a UV-visible spectrometer (Shimadzu, Japan) using quartz cuvettes.

H NMR characterization of p-aminobenzoic acid modied cellulose nanocrystals
A sample of PABA modied CNCs (10 mg) was dissolved in d 6 -DMSO and placed in a 5 mm NMR tube.The 1 H NMR spectrum was recorded by using a Bruker Ascend 400 MHz spectrometer at ambient temperature.

Transmission electron microscopy
The morphology of the fabricated CNCs was analyzed using a Tecnai G2 Spirit (FEI Europe, Eindhoven, The Netherlands) transmission electron microscope.Samples were prepared by diluting each sample with Milli-Q water.A small droplet of the dilution was placed on top of a Butvar-coated copper grid.Any excess amount of the sample was removed from the grid by touching the droplet with a corner of lter paper.The samples were negatively stained by placing a droplet of uranyl acetate (2% w/v) on top of each specimen.Excess uranyl acetate was removed with lter paper, as described above.The grids were dried at room temperature and analyzed at 100 kV under standard conditions.Images were captured using a Quemesa CCD camera, and the width and length of the CNCs were measured using iTEM (Olympus So Imaging Solutions GMBH, Munster, Germany) image analysis soware.In total, 50 CNCs of each sample were measured.The nal results were averaged, and standard deviations were calculated.

X-ray diffraction
The crystalline structure of the PABA modied CNCs was investigated using wide-angle X-ray diffraction (WAXD).Measurements were conducted on a Rigaku SmartLab 9 kW rotating anode diffractometer (Japan) using a Co Ka radiation (40 kV, 135 mA) (l ¼ 1.79030 nm).Samples were prepared by pressing tablets of freeze-dried celluloses to a thickness of 1 mm.Scans were taken over a 2q (Bragg angle) range from 5 to 50 at a scanning speed of 10 s À1 , using a step of 0.5 .The degree of crystallinity in terms of the crystallinity index (CrI) was calculated from the peak intensity of the main crystalline plane (200) diffraction (I 200 ) at 26.2 and from the peak intensity at 22.0 associated with the amorphous fraction of cellulose (I am ), according to eqn (1): 26

CrI
It should be noted that due to the Co Ka radiation source, the cellulose peaks have different diffraction angles compared to results obtained with the Cu Ka radiation source.

Fabrication of the nanocomposite lms
First, 0.88 g of PVA was dissolved in deionized water at 90 C in a round-bottomed ask.Aer allowing the solution to cool, the cellulose nanocrystals were added (0.1-10%, depending on the amount of PVA).The solution was degassed under vacuum suction, followed by casting on a polystyrene tray.The lms were allowed to dry at room temperature for ve days.

Optical transmittance of the nanocomposite lms
The transmittance (190-800 nm) of the nanocomposites was measured with a UV-Vis-NIR spectrophotometer (Carry 500 Scan, Varian Inc., USA), with a step size of 1 nm.

Mechanical properties of the nanocomposites
Tensile tests were performed with a universal material testing machine (Instron 5544, USA), equipped with a 100 N load cell.The PVA-RCNC lms were cut into thin strips, with each specimen having a width of 5 mm.For the tensile testing, a 40 mm gauge length was used at a strain rate of 4 mm min À1 , and six specimens were tested.Using a Hanatek Precision Thickness Gauge Model FT3 (Rhopoint Instruments, UK) thickness tester, the thickness of each specimen was determined as the average of three random locations on the specimen.The lm thicknesses ranged from 14-44 mm.The tests were conducted under 50% relative humidity at a temperature of 23 C and under a prestrain of 0.05-0.1 N. The specimens were conditioned for one day in the measurement environment before testing.Young's modulus was calculated from the initial linear portion of the stress-strain curve, and the ultimate tensile strength was dened as the stress under which the specimen broke.

Results and discussions
In this study, pre-chemical modication of wood cellulose followed by mechanical disintegration was used to fabricate CNCs with UV absorption properties.First, the cellulose was oxidized to dialdehyde cellulose (DAC) with an aldehyde content of 3.85 mmol g À1 (ref.27) prior to the cellulose modication with an amine.In the second step, DAC was then reacted with a sodium salt of PABA in a slightly acidic (pH 5.8) aqueous environment to attach the photoactive groups to the cellulose.PABA was chosen because it exhibits low toxicity and an absorption maximum of 290-320 nm in the UVB region (absorption is due to the aromatic benzene group with amine and carboxylic acid functionalities 28 ).The amino group of PABA is attached to an aromatic ring, which allows the formation of a conjugated imine group by the reaction with aldehyde.Conjugated imine groups are more stable in an aqueous environment than their nonconjugated counterparts, with conjugation also potentially enhancing the light absorption properties. 29Consequently, no reducing agent was required to attach PABA to DAC.The formation of PABA-cellulose (PABAC) can be considered as a "click-type" reaction, as demonstrated in the synthesis route shown in Fig. 1a.The reaction needs only an acid catalyst (water is produced as a by-product), thus increasing the atom economy of the synthesis of photoactive CNCs.
According to the elemental analysis of nitrogen, the PABA group content of PABAC was 0.43 mmol g À1 , indicating that around 12% of the aldehyde groups reacted with PABA.The aldehyde-modication degree was similar to previously reported values for alkylamine-modied 30 and bisphosphonate-modied CNCs 31 obtained by reductive amination of DAC.However, unlike CNCs obtained by reductive amination, the residual aldehydes are not converted to hydroxyl groups but instead appear as free aldehydes or bound to water or hydroxyl groups of cellulose in hydrate or hemiacetal functionality, respectively. 32The residual aldehydes can be utilized in further surface modication (attachment of other chemical groups, such as cross-linking with diamine, 33 or as reducing groups in nanoparticle synthesis 34 ).In addition, aldehydes might also serve as reactive groups for cross-linking with the polymer matrix (amine 35 or hydroxyl groups 25 containing polymers, see the results of the tensile strength measurements below).It should be noted that the residual aldehydes may decrease the stability of cellulosic materials as aldehydes containing cellulose is alkaline labile; 36 however, no signicant effect on the thermal stability has been observed for DAC. 37hemical modication of cellulose with PABA was studied using diffusion reectance infrared Fourier transform spectroscopy (DRIFT).Aer periodate oxidation, a typical C]O stretching vibration band of aldehyde was observed at a wavenumber of 1730 cm À1 (Fig. 1b). 32This band disappeared aer modication with PABA, indicating that the aldehydes reacted with amines to form imines.As shown by an elemental analysis, the aldehydes were only partly modied by PABA, and the remaining aldehydes were masked by the formation of hemiacetals or hydrates aer the reaction with hydroxyl groups of cellulose or water, respectively. 32Aromatic in-ring C-C stretching vibration was seen at 1606 cm À1 , whereas asymmetric vibration of deprotonated carboxylic acid was observed at a wavenumber of 1547 cm À1 .Characteristic aromatic imine bond vibration was observed as a shoulder around 1640 cm À1 . 38his is also the wavenumber of the typical water band observed in cellulose-based materials, which most likely caused the poor separation of the imine band.The shoulder might also be superimposed on the remaining aldehyde and imine bands.
PABA modied CNCs were also studied using 1 H NMR spectroscopy.The local zoom of the 1 H NMR spectrum (4.00-9.00ppm) is presented in Fig. 1c.Typical obscure cellulose proton signals are observed at d H 4.31, 4.70 and 5.44 ppm. 16The aryl proton signals of the PABA substituent can be observed as two clear doublets at d H 6.50 and 7.58 ppm.Moreover, the sharp singlet at d H 8.54 ppm is assigned to the imine proton [39][40][41] which conrms the presence of a covalent bond between the PABA substituent and cellulose backbone.
Aer chemical modications, a 1% PABAC suspension was prepared, and the pH was adjusted to 7 prior to liberation of the CNCs through mechanical disintegration of the modied cellulose.Due to the presence of ionized carboxylic acid groups, the PABAC disintegrated easily to CNCs.The ionized carboxylic acid groups created repulsion between the cellulose bers, improving the disintegration efficiency.The TEM images presented in Fig. 2 conrm the formation of CNCs aer the This journal is © The Royal Society of Chemistry 2016 mechanical disintegration of the PABA-modied cellulose.The width and length of PABAC nanocrystals (PABA-CNCs) were 14.07 AE 6.09 and 177.98 AE 53.31 nm, respectively.The formation of short CNCs instead of CNFs has previously been reported to occur aer the disintegration of chemically modied DAC with an initial aldehyde content higher than 2 mmol g À1 . 31ndividualization of CNCs is thought to be due to the erosion and dissolution of amorphous regions of cellulose bers during chemical modication (during both periodate oxidation and reaction with PABA).This leads to the formation of short CNCs aer mechanical disintegration. 31ased on the WAXD measurements, CrI of the PABA-CNCs was 56% (CrI of the original pulp was 57% 42 ).CrI of PABA-CNCs was similar to the results obtained previously with amino-modied CNCs (53-57%) 16 and slightly higher compared to that of bisphosphonated CNCs (42%). 31This indicates that PABA modication has a similar effect on the crystallinity of cellulose bers compared with reductive amination, which has been used previously to attach functional groups to CNCs.
In the literature, functional nanocelluloses are oen obtained by postchemical treatment.Such treatment may involve solvent exchange and cumbersome and energy-demanding purication of nanosized cellulose entities.The nanocellulose functionalization approach proposed herein uses only water as the solvent, and the desired functional groups can be attached to cellulose prior to its disintegration.Thus, the approach has a number of advantages compared to existing nanocellulose functionalization methods.
The optical properties of the PABA-CNCs dispersed in water (0.1-0.5%) were studied using a UV-Vis spectrometer (Fig. 3a).In the visible light range (380-800 nm), the transmittance of the PABA-CNC suspension (0.1%) surpassed 85%, which is similar to that of CNCs obtained by sequential periodate and chlorite oxidation 25 and signicantly higher than that of alkylaminated CNCs 16 obtained aer reductive amination of DAC.At different concentrations of PABA-CNCs (0.1-0.5%), the transmittance decreased, but it still exceeded 63%, even at a concentration of 0.5% and a wavelength of 380 nm.The results demonstrate the good uniformity and homogeneous nature of the suspensions of PABA-CNCs.The visual appearance of the CNC solutions at different PABA-CNC concentrations is presented in Fig. 3c.
In contrast to nanocellulose produced by periodate oxidation, a sharp decrease in the transmittance (i.e., strong absorption) of the PABA-CNCs was observed below a wavelength of around 340 nm at a concentration of 0.1% (Fig. 2a).A small increase in the transmittance was observed around 280 nm (UVC region).This phenomenon was more visible in the absorption spectra, as shown in Fig. 3b (logarithmic scale).The absorption gradually increased in the UVC region in accordance with an increase in the PABA-CNC concentration, reaching a maximum at a concentration of 0.4%.
The transparency and absorption of the PABA-CNCs were compared to those of reference CNCs (Ref-CNCs), which were fabricated via chlorite oxidation of DAC. 25 The transmittance of the reference CNCs was more than 80% (Fig. 2a), even at the lower end of the spectrum (240 nm).The results clearly show that the incorporation of PABA groups into the cellulose results in the formation of CNCs with strong UV-absorption properties.The visual appearance of the 0.5, 0.4, 0.3, 0.2, and 0.1% PABA-CNCs and 0.1% reference CNC solutions is presented in Fig. 3c.
The feasibility of PABA-CNCs as lightweight bifunctional UVactive reinforcing agents for polymeric materials was studied using poly(vinyl alcohol) (PVA).Different amounts of PABA-CNCs (0.5-10% with respect to the mass of PVA) were dispersed in PVA solutions, followed by solvent casting and drying to obtain self-standing nanocomposite lms.The transmittance of the lms containing the different amounts of PABA-CNCs is presented in Fig. 4a.At the high end of the visible light region (600-800 nm), the addition of the PABA-CNCs to PVA had only a minor effect on the transmittance.For example, the transmittance of the lm containing 0.5% of ller was identical to that of the pure PVA lm.At the low end of the visible light spectrum (380 nm), the transmittance of the lm with 10% of PABA-CNCs was around 80%, indicating that a minimal amount of visible-light absorption or scattering occurred due to the presence of the PABA-CNC llers.The visual appearance of the pure PVA lm and PVA lm with 5% of PABA-CNC is presented in Fig. 4b.
Similar to the PABA-CNC solution spectra, a sharp decrease in transmittance was observed in the UVA region (Fig. 4a).The lowest transmission of the PABA-CNC-containing lms was at 280 nm.At this wavelength, the transmittance of pure PVA was 70%, whereas the transmittance of the PABA-CNCs varied from 43-0%, depending on the concentration of the CNCs.The transmittance of the PABA-CNC-containing lm increased in the UVC region, with the maximum transmission observed at around 240 nm, but it was still signicantly lower than that of the pure PVA lm.For example, the transmission of the lms containing 0.5% and 10% of PABA-CNCs was 54% and 12%, respectively, vs. 70% for pure PVA lm.Consequently, the PABA-CNCs functioned as efficient llers for UV absorption when incorporated into the PVA lms, particularly in the UVA and UVB regions.The latter is important because UVA wavelengths are not absorbed by the ozone layer.The increase in the transmittance in the UVC region strongly indicates that the UV absorption was due to the incorporation of the PABA groups into the cellulose and not light absorption or light scattering by aggregation of CNCs that may have formed during the lm preparation.UV absorption properties of PABA-CNC reinforced PVA lms were similar to those of ZnO-nanoparticle-CNF 22 and lignin-CNC 21 composites.However, with PABA-CNCs, slightly higher UV light selectivity over visible light was observed.
The mechanical properties of the PVA lms improved when the PABA-CNCs were used as llers.The tensile strength is shown in Fig. 5a.There was no signicant difference in the tensile strength when 0.5% and 1% of PABA-CNCs were used, but the tensile strength gradually increased when the amount of PABA-CNCs was increased from 1% to 10%.Compared to pristine PVA, 33% higher tensile strength was obtained using 10% PABA-CNCs.The tensile strengths were only slightly lower  than those reported previously using reactive CNCs (RCNCs) from partially carboxylated DAC containing residual aldehydes (46 MPa vs. 50 MPa). 25The results indicate that the residual unreacted aldehydes of PABA-CNCs functioned as cross-linking agents, resulting in improved mechanical properties.The reinforcing effect of the PABA-CNCs was similar or even higher than that reported for other nanocelluloses. 43he modulus of the PABA-CNC-reinforced PVA increased as a function of the amount ller added (Fig. 5b), with up to a 77% higher modulus achieved using 10% of PABA-CNCs, although some variation occurred.The increase in the modulus was slightly lower than that reported previously for RCNCs, 25 possibly due to the bulky PABA groups vs. the small carboxylic acid groups, but it was well in line with that found in the literature. 43The tensile testing demonstrated that in addition to the novel UV-absorption properties, PABA-CNCs provided a good reinforcing effect to the PVA-lms.
Fig. 5c presents a scheme depicting the action of the reinforced composites containing the UV-absorbing PABA-CNCs.The UV-absorption properties of materials, such as those studied in the present work, are important in several areas, such as when good UV blocking and mechanical strength are required, for example, in contact lenses and sunglasses.Although the utilization of cellulose-based materials under high moisture conditions is limited, the PABA-CNCs described in the present work could be used, for example, as a ller in laminated materials.The incorporation of photoactive CNCs into naturalbased and/or biodegradable polymers could enhance the transparency and UV-absorption properties of materials, whereas a thin-layer hydrophobic laminate could improve the moisture resistance.Surface hydrophobization of photoactive CNC-containing composites with a thin layer of hydrophobic monomers could also be used to improve the moisture resistance of PABA-CNC containing materials.In addition to healthcare applications, photoactive CNCs could function in the preservation of plants as the decrease of the ozone layer and therefore the increase in passing of UV waves, especially UVB, might affect the gene stability of plants. 44Incorporating photoactive CNCs into composites and laminated materials used in greenhouses could help to protect UV-induced plant damage.The excellent mechanical properties of the photoactive CNCs developed in the present work illustrate the feasibility of PABA-CNCs as a ller, especially in load-bearing structures in greenhouses or in everyday wearables, such as sunglasses.

Conclusion
In this study, CNCs with excellent UV absorption properties were successfully fabricated by sequential periodate and "clicktype" imination of wood cellulose bers.The method presented here is straightforward as the chemical modication is performed prior to the liberation of CNCs, eliminating the post-purication steps.PABA-CNCs could then be used as efficient reinforcement and UV absorbing agents for the PVA matrix.Complete elimination of UVA and UVB light was observed by addition of PABA-CNCs to PVA and even in the UVC region the transmittance of the lms with added PABA-CNCs was lower than that of pure PVA.Regardless of the excellent UV absorption, the addition of PABA-CNCs exhibited only a minor effect on the transparency of the PVA lms in the visible-light region.In addition, the PABA-CNCs showed a good reinforcing effect when incorporated into the PVA lms.The results thus far are amongst the rst ones to show simultaneous reinforcing and UV-absorbing effects of CNCs in polymeric nanocomposites.The above-mentioned features of PABA-CNCs could be exploited in numerous applications, which stipulate UV-protection qualities.

Fig. 1
Fig. 1 (a) Schematic illustration of the synthesis of para-aminobenzoic acid-modified cellulose (PABAC) using dialdehyde cellulose (DAC) and a "click-type" reaction (for the sake of clarity, the second aldehyde is drawn in a free form; however, most likely, it forms bonds with the water or hydroxyl groups of cellulose in the hydrates or hemiacetals, respectively).(b) DRIFT spectra of cellulose, DAC, and PABAC.The most distinguishable bands of the chemically modified cellulose are numbered: (1) C]O of aldehyde, (2) COO-of deprotonated carboxylic acid, (3) C-C of an aromatic ring, and (4) C]N of imine, and (c) 1 H NMR spectrum of PABA modified CNCs in d 6 -DMSO.

Fig. 3
Fig. 3 (a) UV-Vis transmittance and (b) absorption spectra of the paraaminobenzoic acid-modified cellulose nanocrystal (PABA-CNC) solutions at different concentrations.The reference CNC was a 0.1% solution of CNCs obtained by the periodate oxidation-based method, without UV absorption groups (see the Experimental section).(c) The visual appearance of the CNC solutions: from right to left 0.5, 0.4, 0.3, 0.2, and 0.1% PABA-CNC and 0.1% Ref-CNC solutions.

Fig. 4
Fig. 4 (a) Transmittance of the pure PVA film and PVA films containing PABA-CNC fillers (0.5-10%), with the dashed line indicating the minimum in the UVB region, and (b) the visual appearance of the pure PVA film (top) and PVA film with 5% of PABA-CNCs.

Fig. 5
Fig. 5 (a) Tensile strength, (b) modulus of the reinforced PVA films as a function of PABA-CNCs and (c) schematic describing the UV-filtering and reinforcing action of the PABA-CNC-containing nanocomposite.