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.     

正交设计法优化大豆分离蛋白膜工艺参数

该文以大豆分离蛋白(SPI)为主要原料,添加甘油制成可食性膜,研究成膜介质和成膜方法对膜性能影响;并比较酸性和碱性条件下可食性膜性能,选择出最佳成膜工艺参数。酸性条件下为:蛋白质与甘油比例为2:1、pH为3、温度80℃、底物浓度8%;碱性条件下为:蛋白质与甘油比例为3:1、pH为10、温度90℃、底物浓度10%。     

Plasticized Whey Protein Edible Films: Water Vapor Permeability Properties

Heat treatment, protein concentration, and pH effects on water vapor permeability (WVP) of plasticized whey protein films were examined. The best film formation conditions were neutral pH, aqueous 10% (w/w) protein solutions heated for 30 min at 90°. Isoelectric point adjustment of whey protein with calcium ascorbate buffer increased WVP with increasing buffer concentration, The importance of vacuum application to minimize film pore size was identified using scanning electron microscopy. Polyethylene glycol, glycerol and sorbitol plasticizer concentration affected film WVP. Determining the effects of relative humidity on WVP for plasticized whey protein films enabled prediction of film behavior under any water vapor partial pressure gradient.     

甘油与甲基纤维素对高直链玉米淀粉- 壳聚糖复合膜性能的影响

以高直链玉米淀粉(HACS)和壳聚糖(CS)为基本材料,甘油为增塑剂,甲基纤维素(MC)为增强剂制备可食性复合膜,研究高直链玉米淀粉与壳聚糖的质量比,甘油的添加量以及甲基纤维素的添加量对复合膜物理性能的影响,包括抗拉强度(TS)、断裂伸长率(E)、水蒸气透过系数(WVP)和色度。结果表明,壳聚糖添加量的增大与甘油添加量的增加都使高直链玉米淀粉- 壳聚糖复合膜的抗拉强度降低,断裂伸长率和WVP 显著增大,膜颜色变黄;甲基纤维素的添加改善了复合膜的机械性能和WVP,随着甲基纤维素添加量的增加,复合膜的抗拉强度和断裂伸长率都随之增大,WVP 逐渐降低,且对膜的颜色没有显著影响。     

Water Vapor Permeability and Mechanical Properties of Soy Protein Isolate Edible Films Composed of Different Plasticizer Combinations

Water barrier and mechanical properties were measured for soy protein isolate (SPI) films plasticized with glycerol (GLY) and 1 of the plasticizers (propylene glycol [PG], polyethylene glycol [PEG], sorbitol [SOR], or sucrose [SUC]) at a ratio of 25:75, 50:50, 75:25, and 0:100. Plasticizer type as well as the plasticizer ratio in the GLY: plasticizer mixtures affected the film water barrier and mechanical properties. An addition of as little as 25% of a less hygroscopic plasticizer in the mixture induced significant reduction in water vapor permeability (WVP) of SPI films. However, at least 50% of the mixture needs to be GLY to show significant improvement in tensile strength (TS). From our experimental design, 50:50 GLY:SOR was the recommended combination because of its comparatively low WVP value and relatively high flexibility and strength. Incompatibility of GLY:PEG plasticizer mixture in SPI film was observed by surface migration of PEG from the film matrix.     

Macromolecular Changes in Extruded Starch‐Films Plasticized with Glycerol,Water and Stearic Acid

Native corn starch, plasticized with water, glycerol and stearic acid, was extruded in a conical twin‐screw extruder and sheeted into 0.4–0.6 mm thick films. The effects of extrusion and plasticizers on gelatinization, as well as the molecular and structural changes, in thermoplastic starch were analyzed. The onset and peak gelatinization temperatures of extruded starch varied from 42–46°C and 52.9–56.9°C, respectively, depending on the glycerol content. The enthalpy of gelatinization of extruded thermoplastic starch in excess water varied from 3.6–7.6 J/g, which also increased with plasticizer content. Amylose‐lipid complexes were formed during extrusion, and their enthalpies depended on the initial stearic acid and moisture contents. High‐performance size‐exclusion chromatography (HPSEC) data revealed that the starch underwent fragmentation during extrusion even under highly plasticized conditions, but the degradation was not severe as compared to previous findings. The relative percentages of amylopectin and amylose in native starch were 76.9 and 23.1%, respectively, which were changed to 71.3–76.6% and 23.4–28.7% in the extrudates. The average molecular weights of amylopectin and amylose in the extrudates ranged from 1.55×10⁷–2.07×10⁷ and 4.35×10⁵–7.39×10⁵, respectively. On the other hand, the molecular weights of amylopectin and amylose in native corn starch were observed as 2.27×10⁷ and 4.68×10⁵, respectively. Cross‐polarization magical angle spinning (CP/MAS) and high‐power decoupling (HP‐DEC) nuclear magnetic resonance (NMR) spectra of thermoplastic starch revealed the characteristics of amylomaize starch, confirming HPSEC results that the amylopectin macromolecules underwent fragmentation into amylose‐like fractions. In the extrudates, glycerol was found to be less mobile and entrained within the starch network.     

Mechanical and Thermal Characteristics of Pea Starch Films Plasticized with Monosaccharides and Polyols

Edible starch films were produced from pea starch and various plasticizers (mannose, glucose, fructose, and glycerol and sorbitol) at the ratio of 4.34, 6.50, 8.69, and 10.87 mmol plasticizer per gram of starch. After film specimens were conditioned at 50% relative humidity, mechanical properties (tensile strength, elongation, and modulus of elasticity), water vapor permeability (WVP), moisture content, and thermomechanical properties (G’ and tan8) were determined as a function of plasticizer concentration. At all concentration levels, monosaccharides (mannose, glucose, and fructose) made the starch films stronger (higher tensile strength) and more stretchable than polyols (glycerol and sorbitol), while WVP of monosaccharide‐plasticized starch films were lower than those of polyol‐plasticized starch films, especially at higher plasticizer concentration levels. Except for 4.34 mmol/g of mannose‐plasticized film, all the other films showed similar modulus of elasticity at the same plasticizer concentration. Polyol‐plasticized films had lower T than the monosaccharide‐plasticized films. Glucose‐ and sorbitol‐plasticized films needed more activation energy to go through glass transition than others. After all, research results showed that not only the polyols but also the monosaccharides were effective in plasticizing starch films. It is concluded that molecular size, configuration, total number of functional hydroxyl group of the plasticizer as well as its compatibility of the plasticizers with the polymer could affect the interactions between the plasticizers and starch molecules, and consequently the effectiveness of plasticization.     

Sensory Attributes of Whey Protein Isolate and Candelilla Wax Emulsion Edible Films

ABSTRACT: Whey protein isolate (5% w/v) films were plasticized with sorbitol or glycerol, and candelilla wax (0.8% w/ v) was added to produce whey protein isolate and candelilla wax emulsion edible films. The films were cut into 7.62 cm × 2.54 cm strips and evaluated by a 15-member trained sensory panel for milk odor, transparency/opaqueness, sweetness, and adhesiveness using a structured 9-point intensity scale. The films had no distinctive milk odor; however, they were perceived to be slightly sweet and adhesive by the trained sensory panel. Whey protein isolate films without candelilla wax were clear and transparent, whereas candelilla wax containing films were opaque.     

Polarity Homogeneity and Structure Affect Water Vapor Permeability of Model Edible Films

A continuous gravimetric measurement method was perfected to determine with accuracy the water vapor permeability of edible films. Two substances, methylcellulose and paraffin wax, with different physicochemical properties, were used as films. Factors affecting permeability included the polarity of film components, the homogeneity or dispersion of material in the film and the structure which depends on the distribution of paraffin wax in the composite films. The thickness and the Water Vapor Transmission Rate (WVTR) measurement methods resulted in different values for permeability. WVTR increased with hydrophilicity and heterogeneity. Modeling trials con-cerning water vapor transport indicated the major influence that structure had on permeability. Waxlaminated fiIms had a very high barrier efficiency, comparable with that of synthetic films.     

Water and Glycerol as Plasticizers Affect Mechanical and Water Vapor Barrier Properties of an Edible Wheat Gluten Film

Glycerol improved film extensibility but reduced film puncture strength, elasticity, and water vapor barrier properties. The plasticizing effect of water was highly temperature dependent. During hydration of gluten film, a sharp decrease in puncture strength, elasticity, and an increase of extensibility and water vapor transmission rate were observed at 5, 30 and 50°C for respective water contents of 30 (0,8 a_w,), 15 (0,7 a_w) and 5% (0,4 a_w). This was related to disruptive water-polymer hydrogen bonding and glass-to-rubber transition.     

蜂蜡和甘油含量对大豆蛋白膜机械性能和阻隔性能的影响

研究添加蜂蜡(质量分数分别为1%、2%、3%、4%、6%、8%和10%)和甘油(质量分数分别为40%和50%)交互作用对大豆蛋白膜机械性能和阻隔性能的影响。结果表明,蜂蜡以固体小颗粒的状态分散于大豆蛋白膜中,能够提高大豆蛋白膜的抗张强度、氧气透过率、阻水性能和表面接触角,降低水蒸气透过率以及断裂延伸率。甘油浓度升高有助于蜂蜡与大豆蛋白分子相结合,提高大豆蛋白膜的综合性能。     

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.     

肉桂醛-大豆分离蛋白可食膜的抑菌及其对冷鲜猪肉的保鲜

本文研究了添加0%,1%,2%,3%,4%,5%和6%肉桂醛含量的大豆分离蛋白膜的水溶性、水蒸气透过系数、抗拉强度和断裂伸长率的变化以及上述膜对大肠杆菌、金黄色葡萄球菌、气假单胞菌和酵母菌的抑菌活性。并研究了添加6%肉桂醛的大豆分离蛋白可食膜在冷藏温度为4℃时对冷鲜猪肉的保鲜效果。结果表明:肉桂醛含量对大豆分离蛋白膜的水溶性、水蒸气透过系数、抗拉强度和断裂伸长率均有一定影响;当大豆分离蛋白膜中肉桂醛含量为3%时能完全抑制大肠杆菌的生长,4%时能完全抑制金黄色葡萄球菌和气假单胞菌的生长,2%时即能抑制酵母菌的生长;且添加肉桂醛含量为6%的大豆分离蛋白可食膜能明显提高冷鲜猪肉的保鲜效果。     

阿魏酸对可食性大豆蛋白膜理化特性的影响

用大豆分离蛋白制备可食性包装膜时，在成膜溶液中添加阿魏酸能增加膜的抗拉强度和断裂伸长率，降低膜的水蒸气透性，并减少甘油用量、提高膜的抗氧化性能。阿魏酸的最适添加量为100mg／100g。其主要机理是阿魏酸与蛋白质的某些氨基酸反应而增加了蛋白质的交联度。由于阿魏酸与蛋白质反应后吸收峰红移，暗示阿魏酸的添加有利于膜防止短波辐射，延长食品保质期。     

Barrier and Tensile Properties of Transglutaminase Cross-linked Gelatin Films as Affected by Relative Humidity, Temperature, and Glycerol Content

Gelatin films were prepared by enzymatic cross-linking with transglutaminase, and their mechanical and barrier properties were evaluated as functions of relative humidity (RH, 30 to 75%), temperature (15 to 35°C) and glycerol content (15 to 31%). Water and glycerol plasticized the films synergistically, resulting in greater elongation but lower tensile strength values. Films with higher glycerol contents exhibited higher moisture contents, indicating higher hydrophilicity of the films. Permeabilities of oxygen and allyl isothiocyanate (an antimicrobial vapor from Cruciferae plants) were low when the films were dry, but increased considerably when RH>50%. Therefore, RH conditions during end-use applications must be considered to optimize the performance of these films.     

Water Vapor Permeability of Caseinate-Based Edible Films as Affected by pH, Calcium Crosslinking and Lipid Content

Edible films were cast from solutions of sodium or calcium caseinate and from emulsions of these proteins with acetylated monoglyceride, beeswax, and stearic acid. The water vapor permeabilities of the films were evaluated at 25°C using the ASTM E96–80 method, modified to calculate the % relative humidity at the film underside. Adjustment to pH 4.6 (isoelectric point), calcium ion crosslinking and combined effects of calcium ascorbate buffer (pH 4.6) reduced water vapor permeability of sodium caseinate films by 36%, 42%, and 43%, respectively. Calcium caseinate-beeswax emulsion films had water vapor permeabilities up to 90% lower than pure sodium caseinate films. Water vapor permeability varied by a factor of two depending on emulsion film orientation, indicating nonisotropic structure.     

Development of Soybean Protein-Isolate Edible Films Incorporated with Beeswax,Span 20, and Glycerol

Abstract: The effect of the beeswax, Span 20, and glycerol content on qualities of soybean-protein-isolate edible films was evaluated. Beeswax and Span 20 were selected to improve qualities of soybean-protein-isolate films from 11 emulsifiers. The content of beeswax, Span 20, and glycerol was further optimized by response surface analysis. The optimal composite emulsifier was beeswax (1.87% of soybean protein-isolate), Span 20 (10.25% of soybean protein-isolate), and glycerol (29.12% of soybean protein-isolate) with tensile strength of 908 MPa, percentage elongation at break of 25.8%, water vapor permeability of 19.2 g/m·d·MPa, and oxygen permeability of 0 cm³/m·d·MPa. The quality of soybean-protein-isolate films incorporated with the optimal composite emulsifier was 2.34 times higher than that of the control. Furthermore, the disulfide bond content of soybean-protein-isolate films showed a positive correlation with their quality, which provided a simple and rapid way to rank quality of soybean-protein-isolate films. Therefore, our result will not only give an instruction to soybean-protein-isolate-film production, but also give a simple and rapid way to rank film qualities. Practical Application: Our results give the optimal composite emulsifiers for the soybean-protein-isolate-film production. The soybean-protein-isolate films based on the optimal composite emulsifiers show their tensile strength of 908 MPa, percentage elongation at break of 25.8%, water vapor permeability of 19.2 g/m·d·MPa, and oxygen permeability of 0 cm³/m·d·MPa, being stronger than the control. Moreover, our results give a simple and rapid way to rank film qualities, because the disulfide bond content of soybean-protein-isolate films showed a positive correlation with their quality. Hence, the disulfide bond content was an indicator to rank qualities of soybean-protein-isolate films.     

可食性魔芋葡甘聚糖成膜特性研究

以魔芋胶 (KG)为基材 ,研究KG的浓度、增塑剂的种类与浓度和干燥温度等因素对膜的抗张强度 (TS)、耐破度 (BS)、伸长率 (E)以及水蒸气透过系数 (WVP)的影响。结果表明 ,随KG浓度的增大 ,各指标均有所升高 ,但浓度太高 (>10 g/L) ,制膜困难 ,且表观性状不够理想。综合考虑 ,浓度以 8g/L为宜 ;随增塑剂浓度的增加 ,膜的TS下降 ,E增大 ,阻湿性能明显降低 ;3种增塑剂中 ,甘油的增塑效果最明显 ,聚乙二醇 4 0 0次之 ,乙二醇最差 ;随干燥温度的提高 ,膜的TS有所增加 ,E和WVP有所降低 ,但温度太高 ,膜显微黄色 ,脆性增大 ,一般 60℃较为理想     

Oil-in-Water Emulsions Stabilized by Sodium Caseinate or Whey Protein Isolate as influenced by Glycerol Monostearate

Competitive adsorption between glycerol monostearate (GMS) and whey protein isolate (WPI) or sodium caseinate was studied in oil-in-water emulsions (20 wt % soya oil, deionized water, pH 7). Addition of GMS resulted in partial displacement of WPI or sodium caseinate from the emulsion interface. SDS-PAGE showed that GMS altered the adsorbed layer composition in sodium caseinate stabilized emulsions containing < 1.0 wt % protein. Predominance of β-casein at the interface in the absence of surfactant was reduced in the presence of GMS. The distribution of α-lactalbumin and β-lactoglobulin between the aqueous bulk phase and the fat surface in emulsions stabilized with WPI was independent of the concentration of added protein or surfactant.