Facile and Green Preparation of Pectin/Cellulose Composite Films with Enhanced Antibacterial and Antioxidant Behaviors

Novel bioactive films based on pectin and cellulose (PC) with different loadings of tea polyphenols and cinnamaldehyde were successfully prepared. A thermal stability was tested, and the results showed that the thermal stability decreased slightly after loading with cinnamaldehyde and tea polyphenols, compared to PC films. The antimicrobial and antioxidant capacities were also investigated. Results showed that PC composite films had good DPPH radical and hydroxyl radical scavenging activities and excellent antibacterial activities against Escherichia coli, Candida albicans and Staphylococcus aureus. Based on the results, the great antioxidant and antibacterial activities of the tea polyphenol and cinnamaldehyde loaded PC films make them suitable for food packaging and preservation.


Introduction
Food packaging materials need to possess good mechanical, air, and moisture barrier properties and be nontoxic. The food packages sold in the market nowadays are petroleum-based plastics, which are non-biodegradable, directly affecting the marine environment and physical security. Moreover, they do not supply any antibacterial or antioxidant performance [1]. Therefore, it is crucial to develop novel food packaging materials that are biodegradable with good antibacterial, antioxidant, and barrier properties, to extend shelf-life and improve food storage effects with environment-friendly activities [2]. Thus, novel films providing green and sustainable packaging activities are relatively attractive [3].
Pectin is a family of polysaccharides and oligosaccharides with diverse structures which is located in the cell wall of most plants, such as apple and citrus [4]. It has a linear structure that is rich in galacturonic acid. The molecular weight of pectin is in the range of 50,000-150,000 Da. Pectin has many different applications depending on its degree of esterification and polymerization [5]. Owing to its bioactivity, biocompatibility, biodegradability, renewability, low cost, and easy modification, pectin is becoming a potential candidate in many fields, such as medical products, cosmetics, bioimplants, drug delivery, tissue engineering, herbicides, and the textile and food industries. Pectin films used in the food industry exhibit good oxygen barrier properties with good hardness and adhesiveness. Despite their advantages, pectin films also present some limitations, such as rigidity and brittleness,

Characterization
A JSM-7600F Scanning Electron Microscope (SEM) operating at an accelerating voltage of 10-15 kV was used to investigate the surface morphologies of the PC and PC5 composite membranes. The samples were coated with a thin layer of platinum under high-vacuum conditions (20 mA, 100 s). FTIR spectra were recorded on a Spectrum Two Spectrometer (Perkin Elmer, Akron, OH, USA) with a wavenumber range of 4000-400 cm −1 at a resolution of 4 cm −1 . Thermogravimetric (TG) analysis was carried out by using a TA Instruments model Q5000 TGA. The samples were heated from 25 to 600 °C with a heating rate of 10 °C/min under nitrogen atmosphere.

Antibacterial and Antifungal Activities
The antibacterial and antifungal activities of the PC composite films were investigated by the disk diffusion method against E. coli, C. albicans, and S. aureus. PC and PC composite films were cut into round shapes with 10 mm diameters, and sterilized by an ultraviolet lamp for 60 min. Lawns of test bacteria (about 1 × 10 5 CFU/plate) were prepared on Tryptone Soya Agar plates. The sterilized films were then carefully placed upon the lawns and placed in a 37 °C incubator for 24 h. Then, the inhibitory action of the tested samples on the growth of the bacteria was determined by measuring the diameters of inhibition zones.

Characterization
A JSM-7600F Scanning Electron Microscope (SEM) operating at an accelerating voltage of 10-15 kV was used to investigate the surface morphologies of the PC and PC 5 composite membranes. The samples were coated with a thin layer of platinum under high-vacuum conditions (20 mA, 100 s). FTIR spectra were recorded on a Spectrum Two Spectrometer (Perkin Elmer, Akron, OH, USA) with a wavenumber range of 4000-400 cm −1 at a resolution of 4 cm −1 . Thermogravimetric (TG) analysis was carried out by using a TA Instruments model Q5000 TGA. The samples were heated from 25 to 600 • C with a heating rate of 10 • C/min under nitrogen atmosphere.

Antibacterial and Antifungal Activities
The antibacterial and antifungal activities of the PC composite films were investigated by the disk diffusion method against E. coli, C. albicans, and S. aureus. PC and PC composite films were cut into round shapes with 10 mm diameters, and sterilized by an ultraviolet lamp for 60 min. Lawns of test bacteria (about 1 × 10 5 CFU/plate) were prepared on Tryptone Soya Agar plates. The sterilized films were then carefully placed upon the lawns and placed in a 37 • C incubator for 24 h. Then, the inhibitory action of the tested samples on the growth of the bacteria was determined by measuring the diameters of inhibition zones.

Antioxidant Activities
The DPPH (2,2 -diphenyl-1-picrylhydrazyl) radical scavenging activities were determined according to the method of Lee et al. [16]. DPPH was dissolved in ethanol to obtain a concentration of Polymers 2019, 11, 57 4 of 11 0.1 mM. PC and PC composite films with diameters of 10 mm were added to 3 mL of DPPH solution and kept in the dark for 30 min at room temperature. Then, the absorbance values of the solution before (A 0 ) and after (A 1 ) treatment with PC-based films were measured at λ = 517 nm. The absorbance of ethanol treated with PC based films (A 2 ) for 30 min at room temperature without any DPPH was also measured. The DPPH radical scavenging percentage was calculated as follows: The capacities of PC and PC composite films to scavenge hydroxyl radicals were measured [16]. Briefly, the reaction systems contained phosphate buffer (1.09 mL, 0.2 M, pH 7.4), 1,10-phenanthroline (0.82 mL, 0.5 mM), ferrous sulfate (0.54 mL, 0.75 mM), and PC-based films in a 10 mL beaker. Then, H 2 O 2 (0.54 mL, 0.01%, v/v) was added and incubated at 37 • C for 60 min. The absorbance values before (A 0 ) and after (A S ) treatment with PC films were measured at λ = 536 nm. De-ionized water was used as the blank, and the absorbance without PC-based films (A b ) was measured at λ = 536 nm. The scavenging percentage of hydroxyl radicals was calculated using the following formula:

Mechanical Properties
The tensile properties of PC and PC 5 films were measured by a dynamic mechanical analyzer (CMT4204, Shenzhen SANS Testing Machine Co., Ltd., Shenzhen, China). Samples were cut manually by a razor blade into strips (50 mm × 5 mm). The static tensile tests were conducted in a ramp displacement mode at an across-head speed of 1 mm/min. Each sample was measured at least five times. The average value and the error bars were calculated.

SEM Morphology
SEM images of PC and PC 5 films at a magnification of 10,000× are displayed in Figure 2. The surface morphology of PC film ( Figure 2A) exhibits a homogenous and smooth surface without any pores. In the case of PC 5 film, it exhibited a rough surface with the presence of some particles, which is shown in Figure 2B. Clearly, the incorporation of cinnamaldehyde and tea polyphenols to PC film did not significantly change the dense surface morphology except for the increase of roughness. Based on SEM analysis, it is apparent that both the surfaces of PC and PC 5 films display dense surface morphologies with no presence of pores.

Antioxidant Activities
The DPPH (2,2′-diphenyl-1-picrylhydrazyl) radical scavenging activities were determined according to the method of Lee et al. [16]. DPPH was dissolved in ethanol to obtain a concentration of 0.1 mM. PC and PC composite films with diameters of 10 mm were added to 3 mL of DPPH solution and kept in the dark for 30 min at room temperature. Then, the absorbance values of the solution before (A0) and after (A1) treatment with PC-based films were measured at λ = 517 nm. The absorbance of ethanol treated with PC based films (A2) for 30 min at room temperature without any DPPH was also measured. The DPPH radical scavenging percentage was calculated as follows: The capacities of PC and PC composite films to scavenge hydroxyl radicals were measured [16]. Briefly, the reaction systems contained phosphate buffer (1.09 mL, 0.2 M, pH 7.4), 1,10phenanthroline (0.82 mL, 0.5 mM), ferrous sulfate (0.54 mL, 0.75 mM), and PC-based films in a 10 mL beaker. Then, H2O2 (0.54 mL, 0.01%, v/v) was added and incubated at 37 °C for 60 min. The absorbance values before (A0) and after (AS) treatment with PC films were measured at λ = 536 nm. De-ionized water was used as the blank, and the absorbance without PC-based films (Ab) was measured at λ = 536 nm. The scavenging percentage of hydroxyl radicals was calculated using the following formula:

Mechanical Properties
The tensile properties of PC and PC5 films were measured by a dynamic mechanical analyzer (CMT4204, Shenzhen SANS Testing Machine Co., Ltd., Shenzhen, China). Samples were cut manually by a razor blade into strips (50 mm × 5 mm). The static tensile tests were conducted in a ramp displacement mode at an across-head speed of 1 mm/min. Each sample was measured at least five times. The average value and the error bars were calculated.

SEM Morphology
SEM images of PC and PC5 films at a magnification of 10,000× are displayed in Figure 2. The surface morphology of PC film ( Figure 2A) exhibits a homogenous and smooth surface without any pores. In the case of PC5 film, it exhibited a rough surface with the presence of some particles, which is shown in Figure 2B. Clearly, the incorporation of cinnamaldehyde and tea polyphenols to PC film did not significantly change the dense surface morphology except for the increase of roughness. Based on SEM analysis, it is apparent that both the surfaces of PC and PC5 films display dense surface morphologies with no presence of pores.

FTIR Characterization
The FTIR spectrum of cellulose is shown in Figure 3A (Curve a). A broad peak ranging from 3700 to 3200 cm −1 is corresponding to the hydroxyl groups and intramolecular hydrogen bond. The peak at 2900 cm −1 is attributed to the CH 2 groups [15]. For Curve b, TP showed typical bands at 1610 and 1510 cm −1 , which correspond to benzene skeleton C=C vibration. The peak at 1690 cm −1 is attributed to C=O stretching [17]. In the case of cinnamaldehyde (Curve c), three characteristic bands at 3027, 1669, and 1624 cm −1 are allocated to C-H, C=O, and the aromatic vibrations, respectively, which is in agreement with previous reports on cinnamaldehyde [18]. There are two bands at 1748 and 1626 cm −1 , attributed to the absorptions by esterified and free carboxyl groups of pectin (Curve d), respectively. For PC composite films ( Figure 3B), all the characteristic bands of cellulose, pectin, TP, and cinnamaldehyde can be found in the FTIR spectra of PC 1 (Curve a), PC 2 (Curve b), PC 3 (Curve c), PC 4 (Curve d), and PC 5 (Curve e). This confirmed the successful preparation of PC composite films.

FTIR Characterization
The FTIR spectrum of cellulose is shown in Figure 3A (Curve a). A broad peak ranging from 3700 to 3200 cm −1 is corresponding to the hydroxyl groups and intramolecular hydrogen bond. The peak at 2900 cm −1 is attributed to the CH2 groups [15]. For Curve b, TP showed typical bands at 1610 and 1510 cm −1 , which correspond to benzene skeleton C=C vibration. The peak at 1690 cm −1 is attributed to C=O stretching [17]. In the case of cinnamaldehyde (Curve c), three characteristic bands at 3027, 1669, and 1624 cm −1 are allocated to C-H, C=O, and the aromatic vibrations, respectively, which is in agreement with previous reports on cinnamaldehyde [18]. There are two bands at 1748 and 1626 cm −1 , attributed to the absorptions by esterified and free carboxyl groups of pectin (Curve d), respectively. For PC composite films ( Figure 3B

Thermogravimetric Analysis
The thermogravimetry was applied to study the weight changes of PC composite film in accordance with increasing temperature, in the form of programmed heating in the range of 25-600 °C under a nitrogen atmosphere. The TG and Differential Thermal Gravity (DTG) spectra of PC and PC5 films are shown in Figure 4A and B, respectively. For PC films (Curve a), they are subjected to a slight weight loss before 100 °C, and then a rapid one in the range of 250-400 °C. The first weight loss was mainly caused by the evaporation of physically adsorbed-and hydrogen bond-linked water molecules, and the second one was due to the thermal degradation and decomposition of cellulose and pectin with the generation of C, CO, CO2, and H2O. The residue of PC film is 4.35%. The maximal decomposition temperature (Tmax) of PC film (Curve a) is 370.8 °C, which can be found in Figure 4B. Two weight loss stages were also displayed in the TGA curve of PC5 films. The residue of PC5 film increased to 8.47% because of the existence of cinnamaldehyde and TP. This result was further confirmed by the shift of the DTG peak from 370.8 to 359.5 °C. Based on these results, the thermal stability slightly decreases after loading with cinnamaldehyde and TP.

Thermogravimetric Analysis
The thermogravimetry was applied to study the weight changes of PC composite film in accordance with increasing temperature, in the form of programmed heating in the range of 25-600 • C under a nitrogen atmosphere. The TG and Differential Thermal Gravity (DTG) spectra of PC and PC 5 films are shown in Figure 4A,B, respectively. For PC films (Curve a), they are subjected to a slight weight loss before 100 • C, and then a rapid one in the range of 250-400 • C. The first weight loss was mainly caused by the evaporation of physically adsorbed-and hydrogen bond-linked water molecules, and the second one was due to the thermal degradation and decomposition of cellulose and pectin with the generation of C, CO, CO 2 , and H 2 O. The residue of PC film is 4.35%. The maximal decomposition temperature (T max ) of PC film (Curve a) is 370.8 • C, which can be found in Figure 4B. Two weight loss stages were also displayed in the TGA curve of PC 5 films. The residue of PC 5 film increased to 8.47% because of the existence of cinnamaldehyde and TP. This result was further confirmed by the shift of the DTG peak from 370.8 to 359.5 • C. Based on these results, the thermal stability slightly decreases after loading with cinnamaldehyde and TP.

Bacterial Inhibition Zones
The disc diffusion method was used to evaluate the bacterial inhibition properties of PC composite films. The bacterial inhibition capacities were estimated by measuring the inhibition zone diameters around the samples after 24 h incubation. Figure 5 shows the inhibition zone pictures. For PC films (a), no inhibition zones were observed at all against E. coli, C. albicans, and S. aureus, indicating that PC films do not possess any bacterial or fungal inhibition abilities. However, after loadings of cinnamaldehyde and TP into PC films, they exhibit clear inhibition zones around E. coli, C. albicans, and S. aureus. Meanwhile, the inhibition ability increases with increasing loadings as well. Figure 6 lists the average inhibition zone diameters of PC composite films. PC1 films had the smallest diameters of inhibition zones of 24, 14, and 22 mm against E. coli, C. albicans, and, S. aureus, respectively. Meanwhile, PC5 films exhibited the best bacterial and fungal inhibition activities, with inhibition zone diameters of 45, 45, and 44 mm against E. coli, C. albicans, and, S. aureus, respectively. It can be clearly seen that the inhibition zone increases with the increase of cinnamaldehyde and TP loadings in the PC composite films. The present study clearly shows that the PC composite films show excellent bacterial and fungal inhibition activities.

Bacterial Inhibition Zones
The disc diffusion method was used to evaluate the bacterial inhibition properties of PC composite films. The bacterial inhibition capacities were estimated by measuring the inhibition zone diameters around the samples after 24 h incubation. Figure 5 shows the inhibition zone pictures. For PC films (a), no inhibition zones were observed at all against E. coli, C. albicans, and S. aureus, indicating that PC films do not possess any bacterial or fungal inhibition abilities. However, after loadings of cinnamaldehyde and TP into PC films, they exhibit clear inhibition zones around E. coli, C. albicans, and S. aureus. Meanwhile, the inhibition ability increases with increasing loadings as well. Figure 6 lists the average inhibition zone diameters of PC composite films. PC 1 films had the smallest diameters of inhibition zones of 24, 14, and 22 mm against E. coli, C. albicans, and, S. aureus, respectively. Meanwhile, PC 5 films exhibited the best bacterial and fungal inhibition activities, with inhibition zone diameters of 45, 45, and 44 mm against E. coli, C. albicans, and, S. aureus, respectively. It can be clearly seen that the inhibition zone increases with the increase of cinnamaldehyde and TP loadings in the PC composite films. The present study clearly shows that the PC composite films show excellent bacterial and fungal inhibition activities.

Bacterial Inhibition Zones
The disc diffusion method was used to evaluate the bacterial inhibition properties of PC composite films. The bacterial inhibition capacities were estimated by measuring the inhibition zone diameters around the samples after 24 h incubation. Figure 5 shows the inhibition zone pictures. For PC films (a), no inhibition zones were observed at all against E. coli, C. albicans, and S. aureus, indicating that PC films do not possess any bacterial or fungal inhibition abilities. However, after loadings of cinnamaldehyde and TP into PC films, they exhibit clear inhibition zones around E. coli, C. albicans, and S. aureus. Meanwhile, the inhibition ability increases with increasing loadings as well. Figure 6 lists the average inhibition zone diameters of PC composite films. PC1 films had the smallest diameters of inhibition zones of 24, 14, and 22 mm against E. coli, C. albicans, and, S. aureus, respectively. Meanwhile, PC5 films exhibited the best bacterial and fungal inhibition activities, with inhibition zone diameters of 45, 45, and 44 mm against E. coli, C. albicans, and, S. aureus, respectively. It can be clearly seen that the inhibition zone increases with the increase of cinnamaldehyde and TP loadings in the PC composite films. The present study clearly shows that the PC composite films show excellent bacterial and fungal inhibition activities.

Antioxidant Properties
DPPH is a stable free radical, and it is usually used for the identification of antioxidant properties [19]. In this study, DPPH radical scavenging assays were performed to evaluate the antioxidant activities of PC composite films. The solution color changes are presented in Figure 7. DPPH is a relatively stable radical which can be reduced to the corresponding hydrazine easily [20]. DPPH was dissolved in ethanol, and showed a deep purple solution. Sample a in Figure 7A is the color of the DPPH solution after treatment with PC films, which exhibits a deep purple. As shown in Figure 7A, the color of the DPPH solution (Sample b) became yellow after treatment with PC1 composite films, indicating that PC1 composite films exhibit some antioxidant properties. With the loading increase of TP in the PC composite films, the color of the DPPH solutions decreased. For PC5 composite films (Sample f), the DPPH solution became light yellow, indicating the good antioxidant ability of PC5 composite films. The DPPH free radical scavenging percentages are shown in Figure 8A. PC composite films without any TP loading have a DPPH free radical scavenging percentage of 33%. Meanwhile, PC1, PC2, PC3, PC4, and PC5 composite films exhibited enhanced DPPH free radical scavenging abilities. With the loading increase of TP in the PC composite films, the scavenging percentages of DPPH free radicals increased from 92% to 97%. This result is constant with the solution color changes shown in Figure 7A.

Antioxidant Properties
DPPH is a stable free radical, and it is usually used for the identification of antioxidant properties [19]. In this study, DPPH radical scavenging assays were performed to evaluate the antioxidant activities of PC composite films. The solution color changes are presented in Figure 7. DPPH is a relatively stable radical which can be reduced to the corresponding hydrazine easily [20]. DPPH was dissolved in ethanol, and showed a deep purple solution. Sample a in Figure 7A is the color of the DPPH solution after treatment with PC films, which exhibits a deep purple. As shown in Figure 7A, the color of the DPPH solution (Sample b) became yellow after treatment with PC 1 composite films, indicating that PC 1 composite films exhibit some antioxidant properties. With the loading increase of TP in the PC composite films, the color of the DPPH solutions decreased. For PC 5 composite films (Sample f), the DPPH solution became light yellow, indicating the good antioxidant ability of PC 5 composite films. The DPPH free radical scavenging percentages are shown in Figure 8A. PC composite films without any TP loading have a DPPH free radical scavenging percentage of 33%. Meanwhile, PC 1 , PC 2 , PC 3 , PC 4 , and PC 5 composite films exhibited enhanced DPPH free radical scavenging abilities. With the loading increase of TP in the PC composite films, the scavenging percentages of DPPH free radicals increased from 92% to 97%. This result is constant with the solution color changes shown in Figure 7A.  Figure 7B shows the solution colors of the tested system after treatment with PC, PC1, PC2, PC3, PC4, and PC5 composite films. The 1,10-phenanthroline-FeSO4-H2O2 system exhibits an orange color. For PC films (Sample a), the solution still shows an orange color. However, the solution color changed to grey after being treated with PC1 composite films (Sample b). The color became dark grey with the increasing TP loadings in the PC composite films (Samples c-f). The scavenging abilities of PC composite films for hydroxyl free radicals are shown Figure 8B. The scavenging abilities of PC composite films for hydroxyl radicals increase significantly as the TP loading increases. Meanwhile, the antioxidant capacities of PC composite films exhibited a TP dose-dependent scavenging activity. The scavenging effect of PC composite films with any TP loading in the PC composite film for hydroxyl radicals is 21%. Whereas, the hydroxyl free radical scavenging percentage for the solution treated with PC1 composite film is 40%. This indicates that PC1 composite films have an increased scavenging ability for free radicals. Moreover, the scavenging activity for hydroxyl radicals increased with increasing TP loadings in the PC composite films. For PC5 composite films, the scavenging percentage for hydroxyl free radicals reached 93%.
Above all, PC films exhibit some DPPH radical and hydroxyl radical scavenging activity. This slight antioxidant activity may be due to the supply of hydrogen by polysaccharides including cellulose and pectin [21]. PC5 composite films have the best scavenging ability against both DPPH free radicals and hydroxyl radicals. The great antioxidant performance is due to the existence of TP in the PC composite films, which can interrupt the chain oxidation reactions by donating a hydrogen atom, acting as an acceptor of free radicals, or by chelating metals [22].  Figure 7B shows the solution colors of the tested system after treatment with PC, PC1, PC2, PC3, PC4, and PC5 composite films. The 1,10-phenanthroline-FeSO4-H2O2 system exhibits an orange color. For PC films (Sample a), the solution still shows an orange color. However, the solution color changed to grey after being treated with PC1 composite films (Sample b). The color became dark grey with the increasing TP loadings in the PC composite films (Samples c-f). The scavenging abilities of PC composite films for hydroxyl free radicals are shown Figure 8B. The scavenging abilities of PC composite films for hydroxyl radicals increase significantly as the TP loading increases. Meanwhile, the antioxidant capacities of PC composite films exhibited a TP dose-dependent scavenging activity. The scavenging effect of PC composite films with any TP loading in the PC composite film for hydroxyl radicals is 21%. Whereas, the hydroxyl free radical scavenging percentage for the solution treated with PC1 composite film is 40%. This indicates that PC1 composite films have an increased scavenging ability for free radicals. Moreover, the scavenging activity for hydroxyl radicals increased with increasing TP loadings in the PC composite films. For PC5 composite films, the scavenging percentage for hydroxyl free radicals reached 93%.
Above all, PC films exhibit some DPPH radical and hydroxyl radical scavenging activity. This slight antioxidant activity may be due to the supply of hydrogen by polysaccharides including cellulose and pectin [21]. PC5 composite films have the best scavenging ability against both DPPH free radicals and hydroxyl radicals. The great antioxidant performance is due to the existence of TP in the PC composite films, which can interrupt the chain oxidation reactions by donating a hydrogen atom, acting as an acceptor of free radicals, or by chelating metals [22].  Figure 7B shows the solution colors of the tested system after treatment with PC, PC 1 , PC 2 , PC 3 , PC 4 , and PC 5 composite films. The 1,10-phenanthroline-FeSO 4 -H 2 O 2 system exhibits an orange color. For PC films (Sample a), the solution still shows an orange color. However, the solution color changed to grey after being treated with PC 1 composite films (Sample b). The color became dark grey with the increasing TP loadings in the PC composite films (Samples c-f). The scavenging abilities of PC composite films for hydroxyl free radicals are shown Figure 8B. The scavenging abilities of PC composite films for hydroxyl radicals increase significantly as the TP loading increases. Meanwhile, the antioxidant capacities of PC composite films exhibited a TP dose-dependent scavenging activity. The scavenging effect of PC composite films with any TP loading in the PC composite film for hydroxyl radicals is 21%. Whereas, the hydroxyl free radical scavenging percentage for the solution treated with PC 1 composite film is 40%. This indicates that PC 1 composite films have an increased scavenging ability for free radicals. Moreover, the scavenging activity for hydroxyl radicals increased with increasing TP loadings in the PC composite films. For PC 5 composite films, the scavenging percentage for hydroxyl free radicals reached 93%.
Above all, PC films exhibit some DPPH radical and hydroxyl radical scavenging activity. This slight antioxidant activity may be due to the supply of hydrogen by polysaccharides including cellulose and pectin [21]. PC 5 composite films have the best scavenging ability against both DPPH free radicals and hydroxyl radicals. The great antioxidant performance is due to the existence of TP in the PC composite films, which can interrupt the chain oxidation reactions by donating a hydrogen atom, acting as an acceptor of free radicals, or by chelating metals [22].

Mechanical Properties
In order to ensure that the PC-based films have good mechanical properties which can be applied for food packaging, tensile stress tests were carried out. The tensile stress, elongation at break, and thickness of PC and PC 5 films are summarized in Table 2. The stress-strain curves are shown in Figure 9, and the inset image is the enlarged curve of PC film. As shown in Table 2, the tensile strengths of PC and PC 5 films were 0.31 and 5.18 MPa, respectively. The tensile strength was highly improved with the incorporation of cinnamaldehyde and TP, which could act as cross-linkers of PC films. Additionally, the elongation at the break decreased from 28.1% for PC films to 7.4% for PC 5 films. Therefore, loading cinnamaldehyde and TP into PC films enhances their mechanical properties, making them more suitable for the application of food packaging.

Mechanical Properties
In order to ensure that the PC-based films have good mechanical properties which can be applied for food packaging, tensile stress tests were carried out. The tensile stress, elongation at break, and thickness of PC and PC5 films are summarized in Table 2. The stress-strain curves are shown in Figure 9, and the inset image is the enlarged curve of PC film. As shown in Table 2, the tensile strengths of PC and PC5 films were 0.31 and 5.18 MPa, respectively. The tensile strength was highly improved with the incorporation of cinnamaldehyde and TP, which could act as cross-linkers of PC films. Additionally, the elongation at the break decreased from 28.1% for PC films to 7.4% for PC5 films. Therefore, loading cinnamaldehyde and TP into PC films enhances their mechanical properties, making them more suitable for the application of food packaging.

Conclusions
The study explored the effects of integration of TP and cinnamaldehyde on the antibacterial and antioxidant properties of biodegradable PC composite films. TG curves showed that the whole thermal stability of PC composite film was slightly decreased with the loading of TP and cinnamaldehyde. The prepared PC composite films displayed a significant inhibitory effect against E. coli, C. albicans, and S. aureus. Meanwhile, they also exhibited good scavenging effects on DPPH and hydroxyl free radicals. Based on the obtained results, the prepared PC composite films could be considered as a potential candidate in the food packaging and preservation field.

Conclusions
The study explored the effects of integration of TP and cinnamaldehyde on the antibacterial and antioxidant properties of biodegradable PC composite films. TG curves showed that the whole thermal stability of PC composite film was slightly decreased with the loading of TP and cinnamaldehyde. The prepared PC composite films displayed a significant inhibitory effect against E. coli, C. albicans, and S. aureus. Meanwhile, they also exhibited good scavenging effects on DPPH and hydroxyl free radicals. Based on the obtained results, the prepared PC composite films could be considered as a potential candidate in the food packaging and preservation field.