Effects of plasticizers, pH and heating of film-forming solution on the properties of pea protein isolate films

Effects of glycerol (3-7% w/w) and sorbitol (4-8% w/w) concentration, pH (7.0, 9.0, 11.0) and heating (90 °C, 20 min) of film-forming solution (FFS) on the water vapor permeability (WVP), moisture content (MC), solubility, light transmission and transparency of pea protein isolate (PPI) films were investigated. Films plasticized with sorbitol exhibited significantly lower WVP, lower MC and higher solubility, in comparison with glycerol-plasticized films. Increasing glycerol content of the films led to increases in WVP and MC but did not affect film solubility. In contrast, increase in sorbitol content had no effect on permeability and MC but resulted in increased film solubility. Moisture sorption isotherms of PPI films suggested that the difference in WVP observed among films plasticized with glycerol and sorbitol might be due to the different hygroscopicity of these plasticizers. The pH of FFS did not have a significant effect on WVP and MC. Solubility of PPI films formed from non-heated FFS was not affected by pH, whereas solubility of films formed from heat-treated FFS generally increased when pH was increased from 7.0 to 11.0. Heating of FFS resulted in improved film transparency. All tested films were characterized by excellent ability to absorb UV radiation. Microstructural observation by scanning electron microscopy did not show differences between sorbitol- and glycerol-plasticized films.     

Design and Characterization of Corn Starch Edible Films Including Beeswax and Natural Antimicrobials

The effectiveness of edible films (EFs) used as coatings to maintain the quality and safety of fresh produce for long time depends on their functional properties characterization. This study was aimed to design and evaluate physicochemical, barrier, mechanical, and antimicrobial properties of EFs based on corn starch (acetylated cross-linked (ACLS) or oxidized (OS)), micro-emulsified beeswax (BW, 0–1 % w/w), and two natural antimicrobials (lauric arginate (LAE, 400–4000 mg/L) and natamycin (NAT, 80–800 mg/L)). EFs based on ACLS or OS made with 1 % BW microemulsion produced homogeneous EFs surface and did not show changes in thickness or opacity. Water vapor permeability (WVP, 0.57 ± 0.04 g mm m^?2 h^?1 kPa^?1 for ACLS, and 0.56 ± 0.05 g mm m^?2 h^?1 kPa^?1 for OS) was reduced; tensile strength (TS, 51.48 ± 5.92 MPa for ACLS, and 40.96 ± 4.98 MPa for OS), and elastic modulus (EM, 211.30 ± 7.85 MPa for ACLS, and 203.50 ± 5.35 MPa for OS) were decreased, whereas elongation at break (E, 4.59 ± 1.11 % for ACLS, and 4.76 ± 4.98 % for OS) increased. The additive effect showed by the combination of natural antimicrobials (2000 mg/L of LAE plus 400 mg/L of NAT) incorporated into EFs with 1 % BW completely inhibited Rhizopus stolonifer, Colletotrichum gloeosporioides, Botrytis cinerea, and Salmonella Saintpaul. These properties of corn starch EFs used as coatings represent an excellent alternative to extend the shelf life of fresh produce.     

Barrier Properties and Surface Characteristics of Edible, Bilayer Films

Various formulations and methods of fabricating a film consisting of edible hydrocolloids and lipids were investigated. Two formulations consisting of a methylcellulose base layer and a beeswax layer, deposited either from a molten state (Wax-M film) or from an ethanolic solution (Wax-S film), were examined for water vapor permeability (WVP), oxygen permeability and other physical properties. WVP values (g-mil-m^?2-day^?1-mm Hg^?1) for the Wax-M and Wax-S films were 0.5 ± 0.05 and 1.6 ± 0.4, respectively. WVP of the two films did not change significantly after storage for 1 wk at -40°C. Oxygen permeability values (g-cm-cm^?2-sec^?1-mm Hg^?1× 10^?12) for the Wax-M and Wax-S films were 0.021 ± 0.002 and 0.007 ± 0.002, respectively. The Wax-M film had a more uniform surface topography than the Wax-S film.     

Preparation and characterization of agar/clay nanocomposite films: the effect of clay type

Abstract: Agar‐based nanocomposite films with different types of nanoclays, such as Cloisite Na⁺, Cloisite 30B, and Cloisite 20A, were prepared using a solvent casting method, and their tensile, water vapor barrier, and antimicrobial properties were tested. Tensile strength (TS), elongation at break (E), and water vapor permeability (WVP) of control agar film were 29.7 ± 1.7 MPa, 45.3 ± 9.6%, and (2.22 ± 0.19) × 10^?9 g·m/m²·s·Pa, respectively. All the film properties tested, including transmittance, tensile properties, WVP, and X‐ray diffraction patterns, indicated that Cloisite Na⁺ was the most compatible with agar matrix. TS of the nanocomposite films prepared with 5% Cloisite Na⁺ increased by 18%, while WVP of the nanocomposite films decreased by 24% through nanoclay compounding. Among the agar/clay nanocomposite films tested, only agar/Cloisite 30B nanocomposite film showed a bacteriostatic function against Listeria monocytogenes.     

冻融处理对淀粉膜结构、热稳定性、机械性能及物理性质的影响

本实验分别以天然马铃薯淀粉（potato starch,PS）、改性马铃薯淀粉（包括羟丙基二淀粉磷酸酯（hydroxypropyl distarch phosphate,HDP）、醋酸淀粉（acetate starch,AS）和氧化淀粉（oxidized starch,OS））为基材,通过流延法制备可食用淀粉膜,考察冻融处理对膜物理性质、机械性能、阻隔性能、微观结构和热稳定性的影响。X射线衍射结果表明,马铃薯来源的淀粉颗粒具有典型的B型晶体结构,在成膜过程中淀粉结晶度降低,冻融处理后淀粉膜晶体峰强度明显减弱。扫描电子显微镜观察结果显示,冻融处理破坏了淀粉膜的微观结构,其中PS膜上出现明显裂纹,AS膜上出现蜂窝和层状结构,而HDP和OS淀粉膜具有更完整的形态。热重分析结果表明,随着温度的升高,淀粉膜的热重曲线出现4 个质量损失阶段,分别对应水分散失、甘油挥发、淀粉解聚及淀粉分解,而冻融处理对膜热稳定性影响较小。常温条件下,PS膜具有最佳的机械性能,其拉伸强度为2.29 MPa,断裂伸长率为68.82%。在3 个冻融循环后,淀粉膜的拉伸强度至少增加了2 倍,断裂伸长率普遍降低,而溶解度和水蒸气透过率仅有轻微变化。综合考虑不同淀粉膜微观结构、机械性能、水蒸气透过率及水溶性,HDP膜表现出更好的冻融稳定性,可应用于冷冻低水分食品的保藏。     

Development of oxidised and heat-moisture treated potato starch film

This study investigated the effects of sodium hypochlorite oxidation and a heat-moisture treatment of potato starch on the physicochemical, pasting and textural properties of potato starches in addition to the water vapour permeability (WVP) and mechanical properties of potato starch films produced from these starches. The carbonyl contents, carboxyl contents, swelling power, solubility, pasting properties and gel texture of the native, oxidised and heat-moisture treated (HMT) starches were evaluated. The films made of native, oxidised and HMT starches were characterised by thickness, water solubility, colour, opacity, mechanical properties and WVP. The oxidised and HMT starches had lower viscosity and swelling power compared to the native starch. The films produced from oxidised potato starch had decreased solubility, elongation and WVP values in addition to increased tensile strength compared to the native starch films. The HMT starch increased the tensile strength and WVP of the starch films compared to the native starch.     

Water Vapor Permeability of Edible Bilayer Films

Edible films composed of a water soluble, carbohydrate layer (hydroxypropyl methylcellulose) and various kinds of lipid layers were tested for resistance to water vapor permeability. Films were tested at 25°C and a relative humidity differential of 85%. Films containing solid lipids, such as beeswax, paraffin, hydrogenated palm oil or stearic acid yielded permeabilities of 0.2 g · mil · day⁻¹· mmHg⁻¹ or less which is a smaller value than that for low density polyethylene.     

Effects of nisin concentration on properties of gelatin film-forming solutions and their films

The addition of nisin into a gelatin matrix can change properties of the film. The aim of this work was to develop gelatin-based films containing different nisin concentrations in order to study their influence on the film's antimicrobial and physical properties and their rheological properties as a film-forming solution (FFS). The FFS was characterised by rheological assays, and the gelatin-based active films were characterised and assessed by the effects of nisin concentrations on their various properties, including antimicrobial activity. Nisin's concentration affected not only its viscoelastic properties of FFS but also its film solubility in water, film surface roughness and light barrier. The addition of nisin also slightly modified the water contact angle and the mechanical properties of the gelatin films. Finally, the films demonstrated activity against Staphylococcus aureus and Listeria monocytogenes at concentrations above 56 mg of nisin g⁻¹ of gelatin.     

Physicochemical Properties of Pin Oak (Quercus palustris Muenchh.) Acorn Starch

Physicochemical properties of acorn (Quercus palustris) starch were studied. Acorn starch granules were spherical or ovoid, with diameters ranging from 3–17 μm. Acorn starch exhibited A‐type X‐ray diffraction pattern, an apparent amylose content of 43.4% and absolute amylose content of 31.4%. Relative to other A‐type starches, acorn amylopectin had a comparable weight‐average molar mass (3.9×10⁸ g/mol), gyration radius (288 nm) and density (16.3 g mol⁻¹nm⁻³). Average amylopectin branch chain‐length corresponded to DP 25.5. Onset gelatinization temperature was 65.0°C and peak gelatinization temperature was considerably higher (73.7°C). The enthalpy change of gelatinization was very high compared to non‐mutant starches (20.8 J/g). An amylose‐lipid thermal transition was not observed. Starch retrograded for 7 d at 4°C had very high peak melting temperature (54.2°C) relative to other A‐type starches. Final (260 RVU) and setback (138 RVU) viscosity of an 8% acorn starch paste was high relative to other starches and pasting temperature was 71.5°C.     

Effects of pH and Salts on Physical and Mechanical Properties of Pea Starch Films

To identify the significant contribution of intermolecular hydrogen bonds of starch molecules to the film structure formation, pH of film‐forming solutions was adjusted and also various salts (NaCl, CaCl₂, CaSO₄, and K₂SO₄) were mixed into the glycerol‐plasticized pea starch film. The film made from pH 7 possessed the highest tensile strength‐at‐break (2 times) and elastic modulus (4 to 15 times) and the lowest elongation‐at‐break compared with those of the films made from acid and alkali environments. The pH 7 film also has the highest film density and the lowest total soluble matter. At the level of 0.01 to 0.1 M of CaSO₄ and 0.1 M of K₂SO₄ in a kilogram of starch, the water solubility of the film increased, while chloride salts slightly lowered the solubility. NaCl and CaSO₄ reduced water vapor permeability (WVP), while CaCl₂ slightly increased WVP at 0.01 and 0.06 M concentrations, and K₂SO₄ significantly increased WVP at 0.03 and 0.15 M. Presence of salts increased tensile strength (5 to 14 times than the control films) and elastic modulus (35 to 180 times) of starch film at 0.01 to 0.03 M of CaSO₄ and K₂SO₄. Elongation‐at‐break increased significantly as salt concentration increases to an optimal level. However, when the concentration exceeded above the optimal level, the E of starch films decreased and showed no significant difference from the control film. Overall, the addition of salts modified physical and mechanical properties of pea starch films more than pH adjustment without any salt addition.     

Water Solubility, Mechanical, Barrier, and Thermal Properties of Cross-linked Whey Protein Isolate-based Films

Water solubility, hermal properties, tensile strength, percent elongation, oxygen permeability (OP), water‐vapor permeability (WVP) of cross‐linked glycerol plasticized whey protein isolate films were studied to determine the effect of cross‐linkers (glutaraldehyde, formaldehyde, dialdehyde starch, carbonyldiimidazole, and UV irradiation) on film properties. With the exception of UV treatment, solubility of the films decreased (P>0.05) upon treatment of the film‐forming solutions with chemical cross‐linkers. Tensile strength increased (P>0.05), whereas percent elongation was not affected by cross‐linking. Chemical cross‐linking increased (P>0.05) WVP and decreased (P>0.05) OP of the films. UV treatment had no effect on WVP and O P. With the exception of UV‐treated films, both onset temperature and degradation temperatures, as determined by differential scanning calorimetry, were increased upon cross‐linking.     

Development and characterization of cassava starch and soy protein concentrate based edible films

The sensory attributes, mechanical, water vapour permeability (WVP) and solubility properties of cassava starch and soy protein concentrate (SPC)‐based edible films of varying levels of glycerol were studied. Addition of SPC and glycerol up to 30% and 20%, respectively, reduced stickiness and improved colour and appearance of the films. Tensile strength (TS), elastic modulus (EM) and elongation at break (EAB) of films increased, while film solubility (FS) and WVP decreased with SPC and glycerol up to 50% and 20% level, respectively, ranging from 20.33 to 26.94 MPa (TS), 41.33 to 72.76 MPa (EM), 7.90 to 12.28 MPa (EAB), 15.07 to 31.90% (FS) and 2.62 to 4.13 g H₂O mm m^?2 day kPa (WVP). The TS, EAB and WVP were higher for the biofilms than for low‐density polyethylene and cellophane films.     

Influence of Water on Molecular and Morphological Structure of Various Starches and Starch Derivatives

In this study the influence of water on untreated, pregelatinised, and chemical modified starches was investigated. Because of their different botanical source, the starch products contain various quantities of amylose and amylopectin. The water vapour absorption capacity of the starches was studied by sorption/desorption and thermogravimetrical measurements. Higher absorption capacities were found for potato starch and for starches containing carboxymethyl and hydroxyethyl groups. Characteristic molecular differences found by Raman spectroscopy were evaluated for untreated and modified starches. To this end, the starch raw materials were classified into groups with similar pretreatments and properties based on cluster analysis. Additionally, the gelatinisation of starch‐water mixtures (gels, powders, and films) was continuously studied using temperature‐dependent Raman spectroscopy. In comparison with powder spectra, the Raman spectra of the starch films showed shifts in band positions in the range of the CH deformation and CH stretching modes. With the exceptions of high‐amylose maize starch and carboxymethylated starch, all starches form films. Starch films differ in their surface structures, water contact angles, and rates of water drop absorption, which might be caused by the different retrogradation properties. The swelling and shrinking behaviour of starch films was investigated at the morphological level by in situ environmental scanning electron microscopy (ESEM) experiments and evaluated by grey value analysis. Films of untreated starch show stronger swelling and shrinking than films of pregelatinised products.     

Solubility Behavior of Granular Corn Starches in Methyl Sulfoxide (DMSO) as Measured by High Performance Size Exclusion Chromatography

The extent of corn starch dispersibility and the relative molecular solubility of amylose and amylopectin in methyl sulfoxide (DMSO) were determined. Granular corn starches with <l, 25, 53, and 70% amylose were dispersed in 0–100% DMSO (in water) solutions at 30°C for 30 min. Maximum dispersibility for all starches (98%) was obtained when 90% DMSO/10% water was used; regular (normal) dent corn starch was equally dispersed in solutions with 88–94% DMSO. Molecular solubility, the presence of individual molecules of amylose and amylopectin, of starches was also measured (after centrifugation and filtration) by high performance size-exclusion chromatography (HPSEC). Starches were dispersed in 90% DMSO and heated for 10 min at temperatures of 35–120ºC. At low temperatures, high coefficients of variation resulted from additional DMSO solubilization after treatment. At 120ºC, 70% amylose starch was >90% solubilized, while waxy starch was only 47% solubilized. When starches were treated for 18–89 h in 90ºC DMSO, solubility stopped increasing after 67 h. High amylose starch (70%) was mostly solubilized, but 53% amylose, waxy and regular starches could only be fully solubilized after exposure to shear. Amylopectin molecules appeared more susceptible to shear induced depolymerization than amylose. The percent amylopectin in the high amylose starches reflected that as determined by iodine binding analysis and the manufacturer; while the percent amylopectin in regular starch was too low (manufacturers: 75%, HPSEC: 65%). Undispersed components were mostly amylopectin. Since amylose is fully solubilized, however, the HPSEC can be used to quickly determine percent amylose in starch.     

Physicochemical,Water Vapor Barrier and Mechanical Properties of Corn Starch and Chitosan Composite Films

Biodegradable flexible films were developed from corn starch (CS) and chitosan (CH); their microstructure, mechanical and barrier properties were evaluated. Chitosan and starch blend filmogenic suspensions showed a pseudoplastic behavior, similar to that of chitosan solutions. Smooth surfaces, homogeneous and compact film structures were observed from microstructure studies using scanning electron microscopy (SEM). The addition of glycerol reduced film opacity and increased film solubility of both CS and composite CS‐CH films. Water vapor permeability values of composite CS‐CH films plasticized with glycerol ranged between 3.76 and 4.54× 10⁻¹¹ g s⁻¹ m⁻¹ Pa⁻¹, lower than those of the single component films. CS‐CH films were resistant and their flexibility increased with glycerol addition. Tensile strength values of CS‐CH films were comparable to those of low‐density and high‐density polyethylenes but lower than that obtained for cellophane, however, composite biodegradable films showed lower elongation at break values than the synthetic commercial ones. In conclusion, CS‐CH films can be described as biofilms with a homogeneous matrix, stable structure and interesting water barrier and mechanical properties, with great possibilities of utilization, and with the advantage of biodegradability.     

Acetylated and native corn starch blend films produced by blown extrusion

Thermoplastic starch (TPS) materials were developed from mixtures of native and acetylated corn starches with glycerol. To optimize the formulations an experimental design for multicomponent mixtures was used and the assayed formulations were determined by statistical software. Blends and pellets humidity content increased with glycerol concentration. Starch destructuration during the extrusion process was studied by thermal analysis. Films presented homogenous structure, rough surfaces and certain stickiness. They presented different properties, related mainly to the differential characteristics of native and acetylated starches and to hydrophilic character of glycerol. Their mechanical behavior indicated that they are a good option as a food packaging materials since TPS films resulted enough resistant to protect the product and flexible to resist moderate deformations. Besides, the use of acetylated starch in the formulations enhanced film resistance and reduced their WVP, despite of its low modification degree. The storage of the films under controlled conditions increased their stiffness, while their flexibility and WVP were reduced. Plasticizer migration towards the matrix surface was observed in stored films. Films resulted stable till a_w = 0.7 and due to their selective gaseous permeability they are useful to package products susceptible to oxidation or to control vegetable respiration and senescence.     

Molecular structure and rheological character of high-amylose water caltrop (Trapa bispinosa Roxb.) starch

The molecular structure and rheological properties of high-amylose water caltrop (Trapa bispinosa Roxb.) starch cultivated in Vietnam were investigated. The water caltrop starch had 47.1% amylose and its molecular weight (Mw) was (4.77±0.27)×10⁶ g/mol, whereas the Mw was (2.07±0.10)×10⁷ g/mol for amylopectin. The average chain length of amylopectin was DP_n=19.0 and the proportions of A, B₁, B₂, and B₃ chains were 28.2, 50.3, 13.1, and 8.5%, respectively. The DSC thermogram of the water caltrop starch was broadly endothermic, with 2 distinct endothermic peaks at 73.6 and 80.7°C. Gel formation of water caltrop starch occurred rapidly, with an extremely high storage modulus up to approximately 1,200 Pa. High-amylose water caltrop starch paste had an extremely high final viscosity compared to that of other cereal starches. These rheological behaviors may have been due to the extremely high amylose content.     

Preparation and characterization of kafirin‐quercetin film for packaging cod during cold storage

This study mainly evaluated the physical properties of kafirin‐quercetin (KQ) edible films and their application on the quality of cod fillets during cold storage. The results showed that the addition of quercetin significantly increased mechanical properties of KQ films, while decreased water vapor permeability, water solubility, and transparency. As quercetin was 0.4% (wt/vol), the film had the highest tensile strength (4.96 ± 1.23 MPa), the lowest water vapor permeability (1.08 ± 0.09 g·mm·m^?2·h·KPa^?1) and water solubility (22.02 ± 0.45%). Moreover, compared with the pure kafirin and polythylene films, KQ films could effectively inhibit the cod meat deterioration by restraining the growth of microorganisms and decreasing TVB‐N and TBARs. The KQ_0.4% film was the best to prolong the shelf life of cod fillets during cold storage. Therefore, KQ edible films could be used as a potential food packaging material to protect and retain the quality of aquatic products.     

Modification of granular corn starch with 4-alpha-glucanotransferase from Thermotoga maritima: effects on structural and physical properties

ABSTRACT:  Corn starch was converted using α-1,4-glucanotransferase from Thermotoga maritima (TmαGT), a hyperthermophilic bacterium, without inducing gelatinization, and the structural changes and physical properties of the modified starches were investigated. Enzyme modification was induced at 65 °C for 8, 16, or 24 h, and the morphology of the modified starches was observed with light and scanning electron microscopy. Granule integrity was mostly maintained after enzyme treatment, although some granules were partially fragmented as evidenced by enlarged surface pores and some cracks. The modified starches had lower apparent amylose levels than raw starch. The molecular weights of amylose and amylopectin molecules in the treated starches were lower than those of raw starch, and the amount of branched molecules, which had much lower molecular weights, also increased in the treated starches. The chain-length distribution of amylopectin showed an increased number of shorter branched chains. The modified starches showed a wider melting temperature range and a lower melting enthalpy than that of raw starch. The X-ray diffraction pattern of the modified starches showed typical A-type starch peaks, but the relative crystallinities were lower than that of raw starch. The solubility and paste clarity of the modified starches were much higher than those of raw starch. The modified starch gels maintained their rigidity over the whole frequency range tested and showed thermoreversibility between 4 and 75 °C. These results suggest that TmαGT can be used to produce granular corn starch, which contains amylose and amylopectin having lower molecular weights and a thermoreversible gelation property.     

Physical properties of cassava starch–carnauba wax emulsion films as affected by component proportions

Properties of glycerol‐plasticised cassava starch–carnauba wax emulsion films were studied as functions of carnauba wax/starch (CW/S) ratios. Increases in CW concentrations improved elongation, but impaired tensile strength and elastic modulus, suggesting a plasticising effect by CW and/or the emulsifier. CW reduced water solubility of the films and decreased their water vapour permeability (WVP) up to CW/S ratios of 0.15–0.20, probably because of the decreased water solubility. Higher CW concentrations resulted in increased WVP, possibly due to starch matrix loosening. The opacity imparted by high CW concentrations in films could compromise some applications. The T_g of starch and the expected CW effects on it were not evidenced by DSC thermograms, but CW seems to have affected starch crystallisation, maybe by forming complexes with amylose and/or amylopectin.