Effect of Plasticizers on Mechanical and Barrier Properties of Rice Starch Film

The effect of plasticizers, glycerol, sorbitol and poly(ethylene glycol) 400 (PEG 400), on mechanical and barrier properties of rice starch film has been investigated. Sorbitol‐ and glycerol‐plasticized starch films appeared homogeneous, clear, smooth, and contained less insoluble particles compared to unplasticized rice starch films. PEG 400 did not form plasticized films of suitable characteristics. The softness and stickiness of films improved with increasing concentrations of glycerol and sorbitol. In general, films plasticized with glycerol and sorbitol displayed a better solubility in water than unplasticized films, i.e. 35% (w/w) glycerol and 45% w/w (sorbitol) (optimum solubility). The tensile strength of films decreased especially in the high concentration regime of plasticizers, between 20–45% (w/w) of plasticizer/rice starch film. Through the entire concentration regime, the tensile strength of glycerol‐plasticized films was significantly lower than that of sorbitol‐plasticized films, but their elongation was larger. The water vapor transmission rate (WVTR) through plasticized films and the oxygen transmission rate (OTR) increased with glycerol and sorbitol concentrations, however, glycerol was revealed to be significantly more effective in reducing the tensile strength as well as increasing the WVTR and the OTR compared to sorbitol. With the higher tensile strength and the smaller OTR and WVTR, the 30% sorbitol‐plasticized film reveals an improved coating performance in terms of a reduction of coating failures.     

Alginate-calcium films: Water vapor permeability and mechanical properties as affected by plasticizer and relative humidity

Alginate films containing dissimilar amounts of guluronate (G) and mannuronate (M): M/G∼0.45 and M/G∼1.5, soaked in a calcium chloride solution up to 20 min were evaluated for water vapor permeability (WVP). M/G∼0.45 films proved to be better moisture barriers at all calcium immersion times compared to M/G∼1.5. WVP of M/G∼0.45 and M/G∼1.5 films decreased as time of immersion in calcium increased; after 3 min, a decrease in WVP was observed. M/G∼0.45 films soaked for 1 min in calcium were further analyzed to determine the effect of plasticizer and relative humidity (RH) on their mechanical properties and WVP, using fructose, glycerol, sorbitol, and polyethylene glycol (PEG-8000). Films without plasticizer showed a lower capacity to adsorb water compared to those with plasticizer. As RH increased, tensile strength (TS) decreased and elongation (E) increased for all films. This effect was more pronounced on films containing plasticizer, which had lower TS at all RHs. Plasticizer did not increase E at 58% RH. At 78% and 98% RH, glycerol, sorbitol and fructose showed a significant increase in E compared to PEG-8000 and no-plasticizer. PEG-8000 provided lower TS and E, while glycerol showed the highest among all plasticizers. There was no difference on WVP between no-plasticizer and glycerol. Fructose and sorbitol showed the lowest WVP while PEG-8000 showed the highest.     

Effects of plasticizers on the properties of edible films from skin gelatin of bigeye snapper and brownstripe red snapper

The effects of type and concentration of plasticizers on the mechanical properties (tensile strength, TS and elongation at break, EAB), water vapor permeability, light transmission, transparency and color of fish skin gelatin edible films from bigeye snapper (Priacanthus marcracanthus) and brownstripe red snapper (Lutjanus vitta) were investigated. At the same plasticizer concentration, fish skin gelatin films from both species plasticized with glycerol (Gly) showed the greatest EAB (P<0.05), whereas ethylene glycol (EG) plasticized films showed the highest TS (P<0.05). Films prepared from brownstripe red snapper skin gelatin exhibited slightly greater TS than those of bigeye snapper skin gelatin (P<0.05) when Gly and sorbitol (Sor) were used. EG, polyethylene glycol 200 (PEG 200) and polyethylene glycol 400 (PEG 400) affected the mechanical properties of both films differently. Films generally became more transparent and EAB, water vapor permeability (WVP), as well as light transmission of films increased, but TS and yellowness decreased with increasing plasticizer concentrations.     

Effect of glycerol on the physicochemical properties of films based on legume protein concentrates: A comparative study

The overall goal of this research was to examine the mechanical, water vapor barrier properties and opacity of films prepared using legume protein concentrates (faba bean, pea, lupin, lentil, and soy) as a function of glycerol concentration (50, 75, or 100% [wt/wt]—relative to the protein weight). Overall, tensile strength (TS) decreased with increasing glycerol concentration, whereas tensile elongation (TE) and water vapor permeability (WVP) increased with increasing glycerol concentration. Film opacity was independent of glycerol concentration. The effect of protein‐type varied considerably depending on the functional property of the film being measured; TS was greatest with faba bean and lowest with lupin, whereas TE was highest for pea, and lowest for soy. Lentil protein films had considerably higher WVP, at the 100% glycerol concentration, as compared to the other protein concentrates. Findings from this study indicate that legume protein concentrates are capable of forming biodegradable, edible films. Overall, pea protein concentrate films showed the most promise for application in terms of strength, elongation, and moisture barrier properties.     

Mechanical and Barrier Properties of Egg Albumen Films

Films were cast and dried from heated, alkaline aqueous egg albumen solutions containing glycerin (GLY) at 30, 40, or 50% w/w of protein, polyethylene glycol (PEG) at 50 or 60%, or sorbitol (S) at 50 or 60% as plasticizers. PEG-plasticized (60%) films also were prepared by substituting 10, 30, 50, or 70% of albumen with yolk solids. Film tensile strength (TS), elongation at break (E), water vapor permeability (WVP), and Hunter color values were measured. At a plasticizer content of 50%, films with S had the lowest WVP while films with PEG had the greatest E. S- and PEG-plasticized films had greater TS than GLY-plasticized films. Yolk solids decreased film TS, E, and WVP while increasing film yellowness.     

Mechanical and water vapor barrier properties of extruded and heat-pressed gelatin films

Gelatin-based edible films were produced by extruding hot melt of gelatin-based resins through a die with slot orifice and followed by heat-pressed method. The resins were plasticized with glycerol, sorbitol and the mixture of glycerol and sorbitol (MGS). The effect of type of plasticizer on extruded and heat-pressed (EHP) film-forming capacity was studied, and the mechanical and water barrier properties of resulting EHP gelatin films were compared with those of gelatin films prepared by solution casting method. Stretchable films were formed when glycerol or MGS were used as plasticizer, whereas resins plasticized with sorbitol were extruded in non-stretchable sheets. Glycerol plasticized gelatin film showed the highest flexibility and transparency among the EHP films tested. Tensile strength (TS), elongation (E) and water vapor permeability (WVP) of glycerol plasticized EHP gelatin films were 17.3 MPa, 215.9% and 2.46 ng m/m² s Pa, respectively, and EHP gelatin films had higher E values, lower TS values and higher WVP values compared to the glycerol plasticized cast gelatin films.     

Effects of various plasticizers and nanoclays on the mechanical properties of red algae film

To manufacture red algae (RA) film, we used various plasticizers such as glycerol, sorbitol, sucrose, fructose, and polypropylene glycol (PPG), and then determined the mechanical properties of the RA films. The tensile strength (TS), elongation at break (E), and water vapor permeability (WVP) of the films containing various plasticizers ranged between 0.43 to 9.10 MPa, 10.93% to 47.17%, and 1.28 to 1.42 ng m/m2sPa, respectively. RA films containing fructose as a plasticizer had the best mechanical properties of all the films evaluated. Incorporation of nanoclay (Cloisite Na+ and 30B) improved the mechanical properties of the films. RA film with 3% Cloisite Na+ had a TS of 10.89, while RA film with 30B had a TS of 10.85 MPa; these films also had better E and WVP values than the other RA films evaluated. These results suggest that RA/nanoclay composite films are suitable for use as food packaging materials. PRACTICAL APPLICATION: Edible RE/nanoclay composite films prepared in the present investigation can be applied in food packaging.     

Development and Characterization of Edible Films from Cranberry Pomace Extracts

The feasibility of using cranberry pomace extract as a new film‐forming material was studied. Cranberry pomaces were extracted using hot water. Low methoxyl pectin (LMP) or high methoxyl pectin (HMP) at a concentration of 0.50% or 0.75% (w/w) and 0.25% (w/w) sorbitol or glycerol was incorporated into film‐forming solutions (FFSs) for improving film functionality. Proximate compositions of cranberry pomace and its extract were determined. The pH and total soluble solid content (SSC) of FFSs, physical and mechanical properties, water vapor permeability, and microstructure of dried films were analyzed. About 1.4% (w/w) of solids was obtained from cranberry pomace water extracts, of which about 93% was carbohydrate. Dried films had bright red color and strong cranberry flavor. Films plasticized with sorbitol were denser in matrix structure and had higher color intensity than those of glycerol plasticized films. In general, LMP and sorbitol incorporated films had higher tensile strength and lower elongation at break and lower water vapor permeability than other films. The higher (0.75%) pectin concentration resulted in increased tensile strength, but decreased elongation at break. Scanning electron microscopy images revealed that sorbitol added films had more regular and compact cross‐section structure than those of glycerol added films. This study demonstrated that it is feasible to create natural colorful and fruit flavor edible films from fruit pomace water extracts. Depending on specific applications of the films, targeted film functionality can be achieved by incorporating proper pectin type and concentration and plasticizer into pomace extracts.     

Mechanical and Barrier Properties of Lactic Acid and Rennet Precipitated Casein-Based Edible Films

Tensile strength (TS), percent elongation (%E), oxygen permeability (OP), and water vapor permeability (WVP) of lactic acid and rennet precipitated casein-based edible films were studied to determine the effect of protein to plasticizer ratio (0.6:1, 1:1, 1.4:1) and plasticizer type (sorbitol, glycerol) on these properties. TS increased (p<0.05) with increase in protein to plasticizer ratio. Sorbitol plasticized films were stronger (p<0.05) than glycerol plasticized films. However, films plasticized with glycerol were more extensible (p<0.05). Film %E decreased with increase in protein/plasticizer ratio for lactic acid casein films, whereas it increased for rennet casein films. Films plasticized with sorbitol were more effective (p<0.05) moisture and oxygen barriers than glycerol plasticized films. Overall, lactic acid casein films plasticized with sorbitol had the most effective mechanical and barrier properties.     

Physical Properties of Gelatin Films Plasticized by Blends of Glycerol and Sorbitol

ABSTRACT: The addition of plasticizers increases the flexibility and workability of films based on biopolymers. However, the use of some plasticizers cause undesirable results, such as the migration of these additives out the film or crystallization during shelf life. Thus, the aim of this study was to evaluate the effect of blends with different ratios of sorbitol and glycerol, at 2 plasticizer concentrations, on mechanical, viscoelastic, and water vapor barrier properties of films based on gelatin. The films were prepared with 2 g gelatin/100 mL of water and with 25 or 55 g plasticizer/100 g gelatin. The ratio, glycerol to sorbitol, was studied as 0:100, 20:80, 40:60, 60:40, 80:20, and 100:0. The increase of plasticizer concentration from 25 to 55 g plasticizer/100 g gelatin caused an increase of flexibility and reduction of resistance and water vapor barrier as expected. In relation to the effect of the mixture, the increase in the proportion of glycerol caused a reduction of the puncture force, tensile strength, modulus of elasticity, and an increase of the puncture deformation, elongation at break, and water vapor permeability due to the higher plasticizing effect of glycerol. This behavior was explained in terms of molecular weight of the plasticizers, which demonstrated that the studied properties could be considered as functions of the number of molecules of plasticizers in the films.     

Genipin交联明胶/溶菌酶缓释抗菌膜材料的微结构与性能研究

针对亲水明胶膜材料对抗菌剂缓释能力较差的问题,采用生物交联剂(genipin)调节膜材料微结构,制备出新型控释明胶/溶菌酶复合膜材料。系统研究了复合膜材料的力学性能、水汽阻隔性能、膨胀性和热性质等物理性能,并用AFM研究了膜材料的表面微结构,探讨了其结构-性能之间的关系。结果表明:genipin交联显著改善复合膜材料的力学性能,TS值从9.72 MPa逐渐增加至18.80 MPa;复合膜材料的膨胀度(swelling)随genipin浓度增加急剧下降,从1316%降至~200%;genipin交联提升复合膜材料的热稳定性。复合膜材的表面粗糙度依赖于genipin浓度,在低浓度段(0~1.0%),膜材料呈现平整表面微结构;高浓度(2.0%)时,膜表面出现不规则的突起,变得粗糙。适度的genipin交联有助于形成有序的三维网络结构,改善复合膜材料的物理性能;高浓度的genipin过度交联明胶基质,形成团聚状聚集物,及弱化明胶分子间相互作用,进而弱化膜材料的水汽阻隔能力。     

Antibacterial activity and mechanical properties of partially hydrolyzed sago starch-alginate edible film containing lemongrass oil

ABSTRACT:  Edible films were prepared from a mixture of partially hydrolyzed sago starch and alginate (SA). Lemongrass oil (0.1% to 0.4%, v/w) and glycerol (0% and 20%, w/w) were incorporated in the films to act as natural antimicrobial agent and plasticizer, respectively. The films were characterized for antimicrobial activity, water vapor permeability (WVP), tensile strength (TS), percent elongation at break (%E), and water solubility (WS). Fourier transform infrared (FTIR) spectroscopy was conducted to determine functional group interactions between the matrix and lemongrass oil. The zone of inhibition was increased significantly ( P < 0.05) by addition of lemongrass oil at all levels in the presence and the absence of glycerol. This indicates that the film containing lemongrass oil was effective against Escherichia coli O157:H7 at all levels. In the absence of glycerol, the tensile strength of film decreased as the oil content increased, but there was no significant ( P > 0.05) difference in percent elongation. The percent elongation at break and WVP values for film with 20% glycerol was found to be increased significantly ( P < 0.05) with an increase in lemongrass oil content. Addition of lemongrass oil did not have any interaction with the functional groups of films as measured by FTIR.     

Mechanical and water vapor barrier properties of tapioca starch/decolorized hsian-tsao leaf gum films in the presence of plasticizer

The objectives of this research were to examine the mechanical and water vapor barrier properties of the starch/decolorized hsian-tsao leaf gum (dHG) films as a function of dHG and glycerol concentration. Edible film-forming solutions were prepared by mixing tapioca starch with dHG at different starch/dHG ratios to make a total solid content of 2%. In total, 15–40% glycerol was then added based on the dry film matter. Starch/dHG films were obtained by casting. It was found that the puncture strength, tensile strength, and modulus as well as the inverse of relaxation coefficient of starch/dHG films pronouncedly increased with increasing dHG, accompanied with a decreasing tendency in puncture deformation and tensile strain at break. Such results implied that starch interacted with dHG synergistically, resulting in the formation of a new network to improve the mechanical properties of tapioca starch/dHG films. Mechanical strengths of starch/dHG films decreased and water vapor permeability (WVP) at 75% RH increased with increasing glycerol concentration. However, the plasticizing effect of glycerol became less significant at high dHG concentration, particularly for the puncture deformation and tensile strain at break of the films. Water sorption isotherm results indicated that significant water sorption would only occur at high water activity (about 0.75), and generally became more pronounced with increasing glycerol and dHG concentration, but to a lesser extent for the latter. Dynamic mechanical analysis revealed that the major glass transition of starch/dHG films occurred at about −50 °C.     

Mechanical,Physical, Antioxidant,and Antimicrobial Properties of Gelatin Films Incorporated with Thymol for Potential Use as Nano Wound Dressing

The aim of this study was to determine the properties of gelatin films incorporated with thymol. Gelatin films were prepared from gelatin solutions (10% w/v) containing thymol (1, 2, 4, and 8% w/w), glycerol (25% w/w) as plasticizer, and glutaraldehyde (2% w/w) as cross‐linker. Cross‐likened films showed higher tensile strength, higher elongation at break, lower Young's modulus, lower water solubility, lower swelling, lower water uptake, and lower water vapor permeability. Incorporation of thymol caused a significant decrease in tensile strength, increase in elongation at break, decrease in Young's modulus, increase in water solubility, decrease in swelling and water uptake, and increase in water vapor permeability slightly. The films incorporated with thymol exhibited excellent antioxidant and antibacterial properties. The antibacterial activity of the films containing thymol was greatest against Staphylucoccus aureus followed by Bacillus subtilis followed by Escherichia coli and then by Pseudomonas aeruginosa. Thus, gelatin films‐containing thymol can be used as safe and effective source of natural antioxidant and antimicrobial agents with the purpose of evaluating their potential use as modern nano wound dressing. Practical Application : This study clearly demonstrates the potential of gelatin films incorporated with thymol as natural antioxidant and antimicrobial nano film. Such antimicrobial films exhibited excellent mechanical, physical, and water activities and could be used as antibacterial nano wound dressing against wounds burn pathogens.     

Mechanical properties of pea starch films associated with xanthan gum and glycerol

The aim of this study was to evaluate the effect of the addition of xanthan gum and glycerol to the starch of green pea with high content of AM (cv. Utrillo) in the preparation of films and their physical characteristics. Filmogenic solution (FS) with different levels of pea starch (3, 4, and 5%), xanthan gum (0, 0.05, and 0.1%), and glycerol (glycerol–starch ratio of 1:5 w/w) were studied. The FS was obtained by boiling (5 min), followed by autoclaving for 1 h at 120°C. The films were prepared by casting. Films prepared only with pea starch were mechanically resistant when compared to other films, prepared with corn, cassava, rice, and even other pea cultivars (yellow, commercial). The tensile strength of these films is comparable to synthetic films prepared with high‐density polyethylene and linear low‐density polyethylene. However, they are films of low elasticity when compared to other films, such as rice starch films, and especially when compared to polyethylene films. The increased concentration of starch in the solution increased the puncture force. The increased concentration of glycerol slightly decreased the film crystallinity and interfered in the mechanical properties of the films, causing reduction of the maximum values of tensile strength, strain at break, and puncture force. The plasticizer also caused an increase of elongation at break. Xanthan gum was important to formation of films; however, it did not affect their mechanical properties.     

Physical Properties of WPI Films Plasticized with Glycerol, Xylitol, or Sorbitol

ABSTRACT: Effects of glycerol, xylitol, and sorbitol on selected physical properties of whey protein isolate (WPI) films were examined. Increasing glycerol or sorbitol content led to increases in moisture content, water vapor permeability, and % elongation; and decreases in tensile strength, elastic modulus, and glass transition temperatures of the films. Increasing levels of xylitol had no effect on permeability, moisture content, or glass transition temperature of the films, but decreased % elongation, tensile strength, and elastic modulus. Moisture content of the films correlated well with glass transition temperatures. Differences in measured physical properties of films with plasticizer type and concentration may be attributed to differences in the hygroscopic and crystalline properties of the plasticizers.     

Mechanical Properties, Water Vapor Permeabilities and Solubilities of Highly Carboxymethylated Starch-Based Edible Films

ABSTRACT: Tensile strength (TS), elongation (E), water vapor permeabilities (WVP) and solubilities were determined for highly carboxymethylated starch (HCMS)-based edible films plasticized with sorbitol (S), xylitol (X), mannitol (M) and glycerol (G). TS and E of HCMS-based film increased as the concentration of plasticizer S, M or × increased. TS of the HCMS-based film containing combined plasticizers were higher than those of films containing single plasticizer. The WVP of HCMS-based films seemed to decreased as the concentration of M, X or G plasticizer increased. Increasing plasticizer concentrations in HCMS-based film resulted in decreasing solubility of the films.     

Physico-mechanical and microstructural properties of semolina flour films as influenced by different sorbitol/glycerol concentrations

This study aimed at investigating the physico-mechanical and microstructural properties of a novel edible film based on plasticized semolina flour with different plasticizer (sorbitol/glycerol, 3:1) contents (30, 40, and 50%, w/w). As plasticizer content increased, water vapor and oxygen permeability, tensile strength, and the elastic modulus of the semolina films decreased, while their water solubility, moisture content, and elongation-at-break increased significantly (p < 0.05). Semolina-based films exhibited excellent absorption of ultraviolet light, and the addition of plasticizers improved the optical properties of the resultant films. Fourier-transform infrared spectroscopy showed no significant effect on the structure of the protein. Thermogravimetric analysis also revealed that increasing plasticizer concentration has no remarkable influence on the magnitude of weight loss. Atomic force microscopy images showed that the surface roughness of the films was influenced by plasticizer concentrations. This study demonstrated that semolina flour protein has the potential to prepare edible films.     

Sorption Characteristics of Soy Protein Films and their Relation to Mechanical Properties

Effects of plasticizers (glycerol, sorbitol, and 1:1 mixture of glycerol and sorbitol) on moisture sorption characteristics of hydrophilic soy protein isolate (SPI) films were investigated at three levels of plasticizer concentration (0.3, 0.5, and 0.7 g plasticizer/g SPI). The combined effects of relative humidity and plasticizer on mechanical properties of soy protein films were also examined. Moisture affinities of soy protein films were affected by hydrophilicity of plasticizer and its concentration. Under given RH conditions, films with higher glycerol ratio absorbed more moisture with higher initial adsorption rate, and films with higher plasticizer contents exhibited higher equilibrium moisture contents. Monolayer moisture contents of SPI films increased as glycerol ratio in a plasticizer mixture and plasticizer concentration increased. Plasticizer and absorbed water loosened the film synergistically, resulting in higher elongation but lower tensile strength. RH effects on mechanical properties of SPI films were varied with plasticizers and their concentration. Films of lower glycerol contents were more sensitive to RH variation as compared to the higher glycerol samples, whereas sorbitol concentration affected the RH region where a sharp decrease in TS value occurred.     

Sorption isotherm and plasticization effect of moisture and plasticizers in pea starch film

Pea starch films were produced with various plasticizers (glucose, fructose, mannose, sorbitol, and glycerol). Effects of plasticizer content (4.34 to 10.87 mmol/g of dry starch) and storage relative humidity (RH) (11.3% to 75.4%) on moisture content (MC), tensile strength (TS), elongation (E), modulus of elasticity (EM), and water vapor permeability (WVP) were evaluated using response surface methodology. MC was influenced strongly by RH. Glycerol-plasticized films had the highest MC, indicating that water molecules played a more important role in plasticizing starch films. Monosaccharide-plasticized films and polyol-plasticized films had similar TS values. However, monosaccharide-plasticized films had higher E values and lower EM values than polyol-plasticized films, meaning monosaccharides had better efficiency in plasticizing starch films. Recrystallization happened in glucose- and sorbitol-plasticized films when they were stored in high RH. Sorption isotherm studies showed the similar adsorption and desorption profiles for all 3 monosaccharide-plasticized films and a hysteresis. The Flory-Huggius model fitted experimental data best for starch films, while the BET model fitted the data marginally.