key: cord-0930531-esoemr8v authors: Harussani, M. M.; Sapuan, S. M.; Firdaus, A. H. M.; El-Badry, Yaser A.; Hussein, Enas E.; El-Bahy, Zeinhom M. title: Determination of the Tensile Properties and Biodegradability of Cornstarch-Based Biopolymers Plasticized with Sorbitol and Glycerol date: 2021-10-27 journal: Polymers (Basel) DOI: 10.3390/polym13213709 sha: 0c42d8ee0ccde20a148da3bf1dbf736bf05e3cb7 doc_id: 930531 cord_uid: esoemr8v In this study, the effects of various quantities of sorbitol and glycerol plasticizers (0%, 30%, 45%, and 60%) on cornstarch-based film were examined to develop a novel polymer for usage with biodegradable materials. The film was prepared using the casting process. According to the test findings, the application of the plasticizer concentrations affected the thickness, moisture content, and water absorption of the film. When plasticizer concentrations were increased to 60%, the tensile stress and Young’s modulus of plasticized films dropped regardless of plasticizer type. However, the thin film with addition of 30% sorbitol plasticizer demonstrated a steady value of Young’s modulus (60.17 MPa) with an increase in tensile strength (13.61 MPa) of 46%, while the lowest combination of tensile strength and Young’s modulus is the film that was plasticized with 60% glycerol, with 2.33 MPa and 16.23 MPa, respectively. In summary, the properties and performance of cornstarch-based film were greatly influenced by plasticizer types and concentrations. The finest set of features in this research appeared in the film plasticized with 30% sorbitol, which achieved the best mechanical properties for food packaging applications. In contrast to biodegradable material, natural chemicals in any accessible human ecosystem are unable to easily decompose. An outstanding example is synthetic plastics, used as the main material in various goods and equipment in engineering, automotive, packaging, and electrical applications [1, 2] . The most sophisticated plastics are designed to be resistant to natural decay, remaining on earth for thousands of years without any degradation [3] . The climate, aquatic or land-originated floras and faunas, and humans are all impacted by plastic pollution [4] . There are two methods of solving this problem: recycling and thermal decomposition, including the incineration and pyrolysis approach [5] . A recycling system is extremely costly since the staff and energy used require significant capital costs. Time and resources are needed for the finished product, including plant covering, washing, drying, grinding, and reprocessing as well as chemical disinfection due to the current COVID-19 pandemic [3, 6] , whereas plastic incineration creates exponentially Cornstarch has been excluded from the system of fresh ear granules [25, 26] . Cornstarch's chemical structure has been studied through recorded procedures [27] . Cornstarch has a fat content of 0.26%, lipid content of 7.13%, and essential protein content of 7.7%. The content of amylose and amylopectin in starch was calculated in the context of the domestic method (food analytical chemistry) of 24.64 g/100 g and 75.36 g/100 g of previous projects, respectively [28] . Cornstarch particles ranged from polyhedral to spherical and the size (89%) of the dispersed particles was less than 40 µm. The starch moisture content was 10.45 g/100 g, and the density was 1.4029 g/cm 3 . Evergreen Technology & Equipment Malaysia Sdn. Bhd. received plasticizers for sorbitol and glycerol. Virtually all plasticizers are compliant with polymers [29] . The shortcomings in plasticizer form and amount used in polymers are widely recognized in the industry. The available thermal and mechanical characteristics [30] , as well as the barrier and rheological properties required, are the selection parameters. Cornstarch films were made using traditional shooting techniques. Filtered 100 mL water containing 10 g pure cornstarch was heated to 85 ± 2 • C for 20 min with continuous thermal baths. This method should have a standardized suspension system. Recommendation research by Ibrahim et al. [31] on sorbitol plasticizer start from 25% to 55% to increase the content of plasticizer. The three forms of plasticizers were then applied to the shaping water individually at 30, 45, or 60% (w/w, dry starch base). The solvent was injected at the same temperature for another 20 min. The slurry will cool until it is poured into a thermal cup. The casting mixture was dehydrated for 15 h in an air circulation oven at 65 • C. The dehydrated film was obtained and stored a week until the characterization process was finished in plastic bags at room temperature. The film consisted of S30%, S45%, S60% for sorbitol; G30%, G45%, G60% for glycerol; SG30%, SG45%, and SG60% for mixture of sorbitol and glycerol; the control for cornstarch for non-plasticized cornstarch film is as described below in Table 1 . Cornstarch films are also made utilizing the same formulation process, in which the plasticizer needs to be injected into suspensions of polysaccharides through a certain amount of cornstarch [32, 33] . The solution is continuously mixed for a while with a magnetic agitator to achieve an acceptable dispersion. The ideal plasticizer is then poured into a polysaccharide blend with a specified weight/weight ratio. The suspension is then positioned in a water tank through a magnetic agitator at the appropriate temperature and period. The standard suspension is then filled in a petri dish as shown in Figure 1 . The dishes are first dried into the air circulation oven. The dry film is then separated into rectangular sections and treated before atmospheric characterization processes [2, 5, 26, [34] [35] [36] [37] . dishes are first dried into the air circulation oven. The dry film is then separated into rectangular sections and treated before atmospheric characterization processes [2, 5, 26, [34] [35] [36] [37] . The thickness of the film was evaluated with a ±0.001 inch precision electronic caliper (Mitutoyo-Co, Tokyo, Japan). The mean of five replicated measurements for each film was used to determine the precise thickness of the film. The film density was specifically determined by its volume (V) and mass (g). Where the diameter of each film is determined from the film tests, measurements indicated (10 mm × 30 mm) times the thickness obtained in the previous stage. A gas pycnometer machine was used to measure the density. Thus, density ( ) is defined as the ratio between the mass (g) and the volume of the specimen ( 3 ). Equation (1) is used to measure the density. (1) The moisture content is defined as the water volume derived from the substance without changing the chemical structure by weight [38] . MC of the film was identified using the method established by Shogren [39] . A common weight film was kept in the oven at 105 °C for 24 h. Shimadzu MOC63u was used to determine the moisture content. For growing specimens shown by percent, weight variations before (W1) and after (W2) heat have been added. Moisture content is measured using Equation (2) . A film sample (15 mm × 15 mm) was dried at a 105 °C temperature in a laboratory oven for 3 h and then the film sample was chilled and weighted right away (mi). The dried sample was submerged in 100 mL of distilled water at room temperature. The sample was immersed in distilled water for 60 min, during which the sample reached equilibrium after around 30 min in water. The sample was pulled from the water after a short immersion period, superficially thawed and weighted with smooth cloth. For the determination of WA, the mass difference between the dry and saturated states in each sample were measured. Equation (3) was used to compute the results of the research. The thickness of the film was evaluated with a ±0.001 inch precision electronic caliper (Mitutoyo-Co, Tokyo, Japan). The mean of five replicated measurements for each film was used to determine the precise thickness of the film. The film density was specifically determined by its volume (V) and mass (g). Where the diameter of each film is determined from the film tests, measurements indicated (10 mm × 30 mm) times the thickness obtained in the previous stage. A gas pycnometer machine was used to measure the density. Thus, density (ρ) is defined as the ratio between the mass (g) and the volume of the specimen (m 3 ). Equation (1) is used to measure the density. The moisture content is defined as the water volume derived from the substance without changing the chemical structure by weight [38] . MC of the film was identified using the method established by Shogren [39] . A common weight film was kept in the oven at 105 • C for 24 h. Shimadzu MOC63u was used to determine the moisture content. For growing specimens shown by percent, weight variations before (W 1 ) and after (W 2 ) heat have been added. Moisture content is measured using Equation (2). A film sample (15 mm × 15 mm) was dried at a 105 • C temperature in a laboratory oven for 3 h and then the film sample was chilled and weighted right away (m i ). The dried sample was submerged in 100 mL of distilled water at room temperature. The sample was immersed in distilled water for 60 min, during which the sample reached equilibrium after around 30 min in water. The sample was pulled from the water after a short immersion period, superficially thawed and weighted with smooth cloth. For the determination of WA, the mass difference between the dry and saturated states in each sample were measured. Equation (3) was used to compute the results of the research. The universal tensile machine, the 5 kN Instron, was used to test the specimens' tensile characteristics. It has been used for the usage of the tensile system and camera tests [5, 30, 40, 41] . A 10 × 90 mm film strip was clamped between tensile handles with a 2 mm/min crosshead ratio and a 30 mm grip distance. Differences in the velocity of the crosshead between 0.5 and 10 mm per minute do not impact the composite's tensile properties. Five studies have been set up to detect tensile strength and elastic modulus. Figures 4-6 shows the 5 kN Instron Tensile Test Machine used in finding the tensile properties. In SPSS software, the acquired experimental findings of tensile strength were subjected to an analysis of variance (ANOVA). Duncan's test was used to do a mean comparison at a significance level of 0.05 (p ≤ 0.05). Figure 2a indicates that with the increase of plasticizer concentration, the thickness of cornstarch-based films dramatically increases. Thus, the films of 60% plasticizers were mostly thicker than the 30-45% plasticizer loading, except for films with sorbitol/glycerol plasticizers. These observations may be relevant in the reconstruction of the polymeric molecular film chain, and the plasticizer position of these findings is important where the higher plasticizer concentration results in a higher weight with the same space and resulted in increased film thickness [42] . In terms of film density, the kind and concentration of plasticizers appeared to have distinct effects. (%) = [ ( − ) ] × 100(3) The universal tensile machine, the 5kN Instron, was used to test the specimens' tensile characteristics. It has been used for the usage of the tensile system and camera tests [5, 30, 40, 41] . A 10 × 90 mm film strip was clamped between tensile handles with a 2 mm/min crosshead ratio and a 30 mm grip distance. Differences in the velocity of the crosshead between 0.5 and 10 mm per minute do not impact the composite's tensile properties. Five studies have been set up to detect tensile strength and elastic modulus. Figures 4-6 shows the 5 kN Instron Tensile Test Machine used in finding the tensile properties. In SPSS software, the acquired experimental findings of tensile strength were subjected to an analysis of variance (ANOVA). Duncan's test was used to do a mean comparison at a significance level of 0.05 (p ≤ 0.05). Figure 2a indicates that with the increase of plasticizer concentration, the thickness of cornstarch-based films dramatically increases. Thus, the films of 60% plasticizers were mostly thicker than the 30-45% plasticizer loading, except for films with sorbitol/glycerol plasticizers. These observations may be relevant in the reconstruction of the polymeric molecular film chain, and the plasticizer position of these findings is important where the higher plasticizer concentration results in a higher weight with the same space and resulted in increased film thickness [42] . In terms of film density, the kind and concentration of plasticizers appeared to have distinct effects. According to Figure 2b , the increase in sorbitol, glycerol, and mixture of sorbitol and glycerol plasticizer concentration in the cornstarch-based film decreased its density: sorbitol from 1.4460 to 1.4340 g/cm 3 , glycerol from 1.3916 to 1.3193 g/cm 3, and mixture of sorbitol and glycerol from 1.4060 to 1.3831 g/cm 3 . This is consistent with the results from previous works [28, 40] . According to Figure 2b , the increase in sorbitol, glycerol, and mixture of sorbitol and glycerol plasticizer concentration in the cornstarch-based film decreased its density: sorbitol from 1.4460 to 1.4340 g/cm 3 , glycerol from 1.3916 to 1.3193 g/cm 3, and mixture of sorbitol and glycerol from 1.4060 to 1.3831 g/cm 3 . This is consistent with the results from previous works [28, 40] . Regardless of the type of plasticizer, adding 30 to 45% plasticizers improved the moisture content of plasticized films due to their water-retaining capacity [43] . However, the effects of sorbitol and glycerol plasticizers decreased moisture content when it reached 60% loading as shown in Figure 3a . Given the glucose unit similarity of the plasticizer's molecular structure, the lack of a molecular connection between the plasticizer and the intermolecular biopolymer chains was caused by differences in the moisture content of plasticized films [44] . As a result, the the likelihood of plasticizers interacting with water molecules has increased [45] . When using natural fiber as an advanced fabric for creating modern product materials, the moisture content is a vital consideration. Low moisture content is required because high water levels adversely affect the composite material's dimensional stability, particularly with regard to mechanical strength, porosity, and waterholding capacity [46] . Polymers 2021, 13, x FOR PEER REVIEW 6 of 12 Regardless of the type of plasticizer, adding 30 to 45% plasticizers improved the moisture content of plasticized films due to their water-retaining capacity [43] . However, the effects of sorbitol and glycerol plasticizers decreased moisture content when it reached 60% loading as shown in Figure 3a . Given the glucose unit similarity of the plasticizer's molecular structure, the lack of a molecular connection between the plasticizer and the intermolecular biopolymer chains was caused by differences in the moisture content of plasticized films [44] . As a result, the the likelihood of plasticizers interacting with water molecules has increased [45] . When using natural fiber as an advanced fabric for creating modern product materials, the moisture content is a vital consideration. Low moisture content is required because high water levels adversely affect the composite material's dimensional stability, particularly with regard to mechanical strength, porosity, and water-holding capacity [46] . One of the most significant constraints of bio-based materials is water absorption. Afterward, the impact of the water absorption rate on the cornstarch-based film was investigated, which was then recorded (Figure 3b ). The physical characteristics of bio-based materials, especially water absorption, are noticeable for their effects on tensile strength, porosity forming, dimensional stability, and the final product swelling [46] . In this study, however, measurements of the water absorption rate 30 min and 60 min after samples' immersion in distilled water were obtained. The cornstarch-based film, using sorbitolplasticized films, showed a strong tendency to absorb water by 176.80% and decrease from 128.18 to 93.34% in water absorption for 45 and 60% plasticizer content. Related testing showed that the glycerol and mixture of sorbitol and glycerol reduced water absorption, from 103.05 to 64.1% for 30-60% glycerol plasticizer and 123.19 to 68.47% for 30-60% sorbitol/glycerol mixture. The decrease in sorbitol and glycerol absorption rates may be due to the role of plasticizing in the development of heavy interfacial bonds within the system to prevent water entry into the matrix [47] . Table 1 describes the results. Control S30% S45% S60% G30% G45% G60% SG30%SG45%SG60% One of the most significant constraints of bio-based materials is water absorption. Afterward, the impact of the water absorption rate on the cornstarch-based film was investigated, which was then recorded (Figure 3b) . The physical characteristics of biobased materials, especially water absorption, are noticeable for their effects on tensile strength, porosity forming, dimensional stability, and the final product swelling [46] . In this study, however, measurements of the water absorption rate 30 min and 60 min after samples' immersion in distilled water were obtained. The cornstarch-based film, using sorbitol-plasticized films, showed a strong tendency to absorb water by 176.80% and decrease from 128.18 to 93.34% in water absorption for 45 and 60% plasticizer content. Related testing showed that the glycerol and mixture of sorbitol and glycerol reduced water absorption, from 103.05 to 64.1% for 30-60% glycerol plasticizer and 123.19 to 68.47% for 30-60% sorbitol/glycerol mixture. The decrease in sorbitol and glycerol absorption rates may be due to the role of plasticizing in the development of heavy interfacial bonds within the system to prevent water entry into the matrix [47] . Table 1 describes the results. In particular, on cornstarch-based films, the tensile strength (TS), Young's modulus (YM), and elongation at break (EB) were assessed using several types of plasticizers. Figures 4-6 illustrate the effect of specific plasticizers on the tensile properties of cornstarchbased film. From the findings, the incorporation of cornstarch and the plasticizer of sorbitol resulted in a significant increase in S30% but then a slight decrease for S45% to S60% in TS and YM but increases in EB were showed along the increase in sorbitol addition. From the findings also, the incorporation of cornstarch and glycerol plasticizer resulted in a slight decrease in TS, YM, and EB compared to the control one. Apart from that, the addition of both plasticizers of sorbitol and glycerol resulted in lower TS and YM than the control sample and continued to decrease but increased in elongation at break for SG30%, SG45%, and SG60%. Note that, as for the statistical analysis, a, b, c and d values with different letters in the same column are significantly different (p < 0.05), as stated in Figures 4-6 . In particular, on cornstarch-based films, the tensile strength (TS), Young's modulus (YM), and elongation at break (EB) were assessed using several types of plasticizers. Figures 4-6 illustrate the effect of specific plasticizers on the tensile properties of cornstarchbased film. From the findings, the incorporation of cornstarch and the plasticizer of sorbitol resulted in a significant increase in S30% but then a slight decrease for S45% to S60% in TS and YM but increases in EB were showed along the increase in sorbitol addition. From the findings also, the incorporation of cornstarch and glycerol plasticizer resulted in a slight decrease in TS, YM, and EB compared to the control one. Apart from that, the addition of both plasticizers of sorbitol and glycerol resulted in lower TS and YM than the control sample and continued to decrease but increased in elongation at break for SG30%, SG45%, and SG60%. Note that, as for the statistical analysis The results show that the maximum tensile strength is S30% with 13.61 MPa, larger than G30% with 2.53 MPa and SG30% with 5.74 MPa. The predicted concept of low plastic strain is related to hydrogen interactions between starch and plasticizer molecules, which are tightly controlled and decrease in quality by decreasing plasticizers [48] . Therefore, the tensile strength for sorbitol-plasticized film then decreased from 13.61 to 4.49 MPa and the mixture of sorbitol and glycerol-plasticized film decreased from 5.74 to 2.26 MPa as plasticizer concentration increased to 45% and 60%. While the plastic films registered the lowest stress levels, they decreased the plasticizer from 2.53 to 2.33 MPa as shown in Figure 4 . Many researchers have shown that the tensile strength of starch films declines due to the enhanced plasticizer concentration. Young's modulus helps determine the stiffness of materials. The optimal tensile strength of a material is indicated by a greater Young's modulus value. The figure shows the impact of the cornstarch-based film on the corresponding tensile strength and Young's modulus for different plasticizers with different concentrations (30-60%) . The rise in plasticizer concentrations, from 30 to 60%, shows substantial reductions in Young's modulus: 60. 17-15.35 MPa for sorbitol-plasticized films; 47.17-11.88 MPa for sorbitol/glycerolplasticized films; and 19. 43-16.23 MPa for glycerol-plasticized films. These plasticizers are incorporated into starch chains, promoting the formation of hydrogen bonds between molecules while decreasing the starch matrix's strong intramolecular attraction. The Young's modulus for cornstarch-based film is thus smaller and less rigid [29, 49] . The results show that the maximum tensile strength is S30% with 13.61 MPa, larger than G30% with 2.53 MPa and SG30% with 5.74 MPa. The predicted concept of low plastic strain is related to hydrogen interactions between starch and plasticizer molecules, which are tightly controlled and decrease in quality by decreasing plasticizers [48] . Therefore, Control S30% S45% S60% G30% G45% G60% SG30%SG45%SG60% The results show that the maximum tensile strength is S30% with 13.61 MPa, larger than G30% with 2.53 MPa and SG30% with 5.74 MPa. The predicted concept of low plastic strain is related to hydrogen interactions between starch and plasticizer molecules, which are tightly controlled and decrease in quality by decreasing plasticizers [48] . Therefore, Control S30% S45% S60% G30% G45% G60% SG30%SG45%SG60% Based on the elongation at break value of the cornstarch-based film with a plasticizer of sorbitol, glycerol, and a mixture of sorbitol/glycerol, the thin film resulted in a different effect, as can be seen when compared with the tensile strength and Young's modulus values ( Figure 6 ). As the pressure increases, the elongation at break of the cornstarch-based film with sorbitol and sorbitol/glycerol plasticizer increases. However, the cornstarch-based film with only glycerol plasticizer shows a decrease in elongation at break. This shows the sorbitol plasticizers will produce higher elongation at break while glycerol plasticizer will produce lower elongation at break [33] . The extendibility of the material is calculated from the original length before the breakpoint. With the reconstruction of the composite structure, by strengthening intermolecular links between cornstarch and plasticizer, the film elongation is decreased as the fiber loading is increased. This redesign increases rigidity and durability and reduces chain instability [50] . To solve persistent environmental issues caused by the manufacturing of non-biodegradable polymers, the creation of completely biodegradable films is necessary. Cornstarch is taken from corn plant components, and the properties of cornstarch-based film have also been found to be influenced by different plasticizers that are effectively defined. Furthermore, the intrinsic disadvantages of cornstarch-based films, such as brittleness, inferior mechanical properties, as well as weak water barrier resistance, have restricted their use as a biomaterial. This research intended to improve the functional characteristics of cornstarch. The cornstarch material has also been tested for mechanical and physical properties. Tensile strength, Young's modulus, elongation at break, density, moisture content, and water absorption of the cornstarch-based film have all been researched to reduce the disadvantages and maximize the efficiency of cornstarch-based film. The key aim was to determine the effect of various concentrations of sorbitol, glycerol and a sorbitol/glycerol in plasticizers to develop specific polymers for use in biodegradable goods. The solution casting technique was used for the creation of films in this study. Based on the results, the addition of the plasticizers changed the thickness, moisture content, and water absorption. Tensile strength and Young's modulus dropped when the plasticizer concentration was above 30%, regardless of the plasticizer type. In conclusion, the characteristics and performance of the cornstarch-based film have a considerable impact on the plasticizer kinds and concentrations. The maximum level of mechanical efficiency was reached with film plasticized with 30% sorbitol, with tensile strength and Young's modulus of 13.61 MPa and 60.17 MPa, respectively. The biopolymer films revealed a novel cornstarch waste resource that is both environmentally beneficial and simple to produce. It also generated new data on the interactions of various plasticizer types and how their concentration affects film capabilities, which might benefit the development of biodegradable materials. For future endeavors, there are several improvements and research that should be worked on: 1. The analysis of hybrid corn compounds should be regarded using certain processing methods for different forms of goods such as extrusion or injection. The research will be carried out to further increase the efficiency through different surface treatment methods of hybrid corn plant composites. Experiments in synthetic polymer films on the potency of natural antimicrobial compounds should be regarded to develop their performance. Experiments should often be taken into consideration to validate the effects of current research using finite element methods. 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Cassava starch-green coir fibers from Brazil Comparative study of film forming behaviour of low and high amylose starches using glycerol and xylitol as plasticizers Tensile, barrier, dynamic mechanical, and biodegradation properties of cassava/sugar palm fiber reinforced cassava starch hybrid composites Development of oxidised and heat-moisture treated potato starch film The authors would like to acknowledge the financial support from Taif University Researchers Supporting Project Number (TURSP-2020/106), Taif University, Saudi Arabia and Geran Putra Berimpak (GPB), UPM/800-3/3/1/GPB/2019/9679800. Next, special thanks to Universiti Putra Malaysia for providing us research facilities. The authors declare no conflict of interest.