Bitterness reduction in grapefruit juice through active packaging

Naringin and limonin are the principle bitterness components of citrus juices. Our objective was to determine if the perceived bitterness in grapefruit juice could be reduced during storage through interaction with active packaging film. Storage of 10° Brix grapefruit juice at 7°C in contact with fungal-derived naringinase immobilized on cellulose acetate film reduced bitterness as perceived by a sensory panel. The films reduced naringin and limonin concentration by hydrolysis and adsorption respectively. Reduction in the naringin and limonin content of grapefruit juice by cellulose acetate films containing immobilized enzyme from 600–400 mg/l and 8.0–6.7 mg/l respectively could be detected as a reduction in bitterness by a sensory panel (p < 0.10). As the area of film (cm²)/volume of juice (ml) ratio increased from 1.1 to 3.6, the time to decrease the naringin level decreased. The reduction in naringin was not affected by agitation or holding the samples quiescently. The amount of enzyme desorbed from the film represented only 2% of the amount of enzyme immobilized in the film. The reduction in bitterness comes from direct interaction with the active packaging films. © 1998 John Wiley & Sons, Ltd.     

Development and evaluation of an edible antimicrobial film based on yam starch and chitosan

Edible antimicrobial films are an innovation within the biodegradable active packaging concept. They have been developed in order to reduce and/or inhibit the growth of microorganisms on the surface of foods. This study developed an edible antimicrobial film based on yam starch (Dioscorea alata) and chitosan and investigated its antimicrobial efficiency on Salmonella enteritidis. A solution of yam starch (4%) and glycerol (2%) was gelatinized in a viscoamilograph and chitosan added at concentrations of 1%, 3% and 5%. Films with and without chitosan were produced by the cast method. To evaluate the antimicrobial activity of the films, two suspensions of S. enteritidis were used in BHI medium, corresponding to counts of 2 × 10⁸ and 1.1 × 10⁶ CFU/ml. The suspensions (50 ml) were poured into flasks. The films were cut into 5 × 5 and 5 × 10 cm rectangles to be used at ratios of 1 : 1 (1 cm²/ml microorganism suspension) and 2 : 1 (2 cm²/ml). The film 30 µm thick on average. As a control, pure chitosan at an amount corresponding to that contained in the 3% and 5% films (5 × 10 cm) was added to flasks containing the microorganism suspension. Also, flasks containing only a suspension of S. enteritidis were used as control. The suspensions, in flasks, were kept at 37°C in a waterbath with agitation. Suspension aliquots were removed every hour for reading the optic density (OD₅₉₅) and plating onto PCA medium. The results showed that chitosan has a bactericidal effect upon S. enteritidis. Films treated with chitosan at different concentrations showed similar antimicrobial efficiency, in addition to being dependent on diffusion. The chitosan‐treated films caused a reduction of one to two log cycles in the number of microorganisms, whereas the pure chitosan presented a reduction of four to six log cycles compared with the control and starch film. The films showed good flexibility. Copyright © 2005 John Wiley & Sons, Ltd.     

Antimicrobial activity of glucose oxidase‐immobilized plasma‐activated polypropylene films

Antimicrobial enzyme, glucose oxidase (GOX), was covalently immobilized onto amino‐ and carboxyl‐plasma‐activated biorientated polypropylene films (BOPP) via glutaraldehyde and carbodiimide chemistries. N₂‐plasma + NH₃ and N₂‐plasma + CO₂ treatments were utilized to create amino (1.1 nmol/cm²) and carboxyl (0.9 nmol/cm²) groups densities onto the surface of BOPP films. GOX‐immobilized onto amino‐activated BOPP films using 2.5% glutaraldehyde produced higher enzymatic activities than GOX‐immobilized by 0.4% carbodiimide. Further immobilizations were carried out with glutaraldehyde as the coupling agent at temperatures of 4–75°C at pH 5.6 and 7.2. 10 s treatment was sufficient to immobilize GOX at high temperatures in both pH conditions, producing enzymatically active films which remained active over 30 days of storage. GOX covalently immobilized onto BOPP films completely inhibited the growth of Escherichia coli and substantially inhibited the growth of Bacillus subtilis; thus, they may have great potential to be exploited in various antimicrobial packaging film applications. Copyright © 2005 John Wiley & Sons, Ltd.     

Improvement of physical properties of IGZO thin films prepared by excimer laser annealing of sol–gel derived precursor films

Indium gallium zinc oxide (IGZO) transparent semiconductor thin films were prepared by KrF excimer laser annealing of sol–gel derived precursor films. Each as-coated film was dried at 150 °C in air and then annealed using excimer laser irradiation. The influence of laser irradiation energy density on surface conditions, optical transmittances, and electrical properties of laser annealed IGZO thin films were investigated, and the physical properties of the excimer laser annealed (ELA) and the thermally annealed (TA) thin films were compared. Experimental results showed that two kinds of surface morphology resulted from excimer laser annealing. Irradiation with a lower energy density (≤250 mJ cm⁻²) produced wavy and irregular surfaces, while irradiation with a higher energy density (≥350 mJ cm⁻²) produced flat and dense surfaces consisting of uniform nano-sized amorphous particles. The explanation for the differences in surface features and film quality is that using laser irradiation energy to form IGZO thin films improves the film density and removes organic constituents. The dried IGZO sol–gel films irradiated with a laser energy density of 350 mJ/cm² had the best physical properties of all the ELA IGZO thin films. The mean resistivity of the ELA 350 thin films (4.48 × 10³ Ω cm) was lower than that of TA thin films (1.39 × 10⁴ Ω cm), and the average optical transmittance in the visible range (90.2%) of the ELA 350 thin films was slightly higher than that of TA thin films (89.7%).     

Rapid Thermal Annealing of ZnO Nanocrystalline Films for Dye-Sensitized Solar Cells

Nanocrystalline ZnO thin films were prepared by the sol–gel method and annealed at 600 °C by conventional (CTA) and rapid thermal annealing (RTA) processes on fluorine-doped tin oxide (FTO)-coated glass substrates for application as the work electrode for a dye-sensitized solar cell (DSSC). ZnO films were crystallized using a conventional furnace and the proposed RTA process at annealing rates of 5 °C/min and 600 °C/min, respectively. The ZnO thin films were characterized by X-ray diffraction (XRD) and atomic force microscopy (AFM) analyses. Based on the results, the ZnO thin films crystallized by the RTA process presented better crystallization than films crystallized in a conventional furnace. The ZnO films crystallized by RTA showed higher porosity and surface area than those prepared by CTA. The results show that the short-circuit photocurrent (J _sc) and open-circuit voltage (V _oc) values increased from 4.38 mA/cm² and 0.55 V for the DSSC with the CTA-derived ZnO films to 5.88 mA/cm² and 0.61 V, respectively, for the DSSC containing the RTA-derived ZnO films.     

Tuned photoluminescence from Si-implanted SiO2 films with rapid and conventional thermal annealing

In this study, by using a conventional thermal annealing (CTA), the obviously near-infrared shift and intensity amplification of room-temperature photoluminescence (PL) spectrum could be observed from the 3 × 10¹⁶ cm⁻² Si⁺-implanted 400-nm-thick SiO₂ films after rapid thermal annealing (RTA) at 1150 °C in dry nitrogen. For isothermal RTA durations ≥20 s at the heating rate of 100 °C/s, the PL peaks from the only RTA-treated films were detected around 1.7 eV and, for 1050 °C CTA durations between 1 and 3 h, no significant PL could be found from the only CTA-treated films. However, when annealing the RTA-treated films with the CTA for only 1 h, then, we varied the terminal PL-peak from 1.7 to 1.5 eV and obviously increased their respective intensities from the films. These results are attributed to the variation of silicon nano-crystals embedded in SiO₂ film.     

The temperature dependence of stresses in aluminum films on oxidized silicon substrates

In situ measurements were carried out of stress at the AlSiO₂ interface at various temperatures (25–500 °C) and for various film thicknesses (0.2–1.6 microm). These data are complemented with microstructural studies by transmission electron microscopy.For the aluminum films studied, the intrinsic structural component was very small (less than 2 × 10⁸ dyn cm^?2). On heating, thermal mismatch led to a compressive stress, with dσ/dT ≈ ?2 × 10⁷ dyn cm^?2 °C; these films yielded at 6σ6 ; ? 5 × 10⁸ dyn cm^?2, primarily through diffusion creep and grain growth. On cooling from about 450–500 °C, thermal mismatch led to a tensile stress which was limited mainly by dislocation slip. The final room temperature value after thermal cycling ranged from 0.5 × 10⁹ dyn cm^?2 for a 1.5 microm film to 8 × 10⁹ dyn cm^?2 for a 0.2 microm film; these values are believed to represent the critical stress for the generation of dislocation loops within the grains.The grain size of cold-deposited aluminum films ranged from about 0.2 microm for films 0.45 microm thick to about 2 microm for films 1.5 microm thick. Thermal cycling led to an order-of-magnitude increase in the grain size together with the formation of dislocation networks within the grains.     

Stress cracking of nylon polymers in aqueous salt solutions

Craze-growth kinetics were measured for nylon 6 and nylon 6,6 immersed in aqueous salt solutions. Under all conditions of stress level, temperature, and salt type examined, the craze growth data exhibited a steady state growth rate which was linear with time. Comparison of these results with available mechanistic models for craze growth suggests that salt-induced crazing of nylon polymers is an example of relaxation-controlled craze growth. Activation energies for crazing are 2.1 × 105 J mol^–1 for nylon 6 and 3.9 x 10^–5 J mol^–1 for nylon 6,6. These values are similar to the activation energies for the alpha relaxation (glass transition) of the nylons. Although the activation energies depend to some extent on the initial stress intensity factor level and salt type, the results indicate that the polymer type is the primary factor determining the temperature dependence of craze growth. The effect of salt type on cracking was shown to correlate with the charge density ratio of the salt cation, namelyQ/R, whereQ is the oxidation number andR is the ionic radius. These results indicate that the stress cracking susceptibility of nylon polymers can be predicted based upon the polymer chemical structure, glass transition temperature, degree of crystallinity, and theQ/R ratio of the specific salt in question.     

Effect of ovenproof plastic films on the quality of spotted rose snapper (lutjanus guttatus) fillets during frozen storage

Spotted rose snapper (Lutjanus guttatus) fillets packed in two polymer films, polyamide 6,6 (PA66) and polyethylene terephthalate (PET), were stored at ?20°C for a period of 120 days. Films were tested for melting temperature (PA66 253–257°C and PET 252–255°C), oxygen transmission rate [PA66 51.8 ± 12.9cm³/(m²·24h·atm) and PET 152.7 ± 0.2cm³/(m²·24h·atm)] and water vapor transmission rate [PA66 17.8 ± 1.7g/(m²·24h) and PET 6.5 ± 0.2g/(m²·24h)]. Sensory analyses (firmness, flavour and appearance) were performed at 0, 30, 60, 90 and 120 days of storage after baking the fillets in the same storage bags. For raw fillets, their water‐holding capacity (WHC), total aerobic counts (TAC), pH, trimethylamine (TMA) and shear‐force resistance were measured at the same periods. Sensory analyses after baking showed no differences between the fillets packaged in the two films. The WHC, TAC, pH and TMA values in both products were kept within accepted limits. The fillets packed in PET showed a significant increase in firmness (shear‐force resistance) during the first 60 days of storage and then a decrease at 90 days due to dehydration through the film seals. Over the same period, the fillets packed in PA66 showed no significant changes in firmness. In this study, it was demonstrated that it is possible to develop a ready‐to‐bake fish fillet product by using ovenproof films for packaging during storage. Copyright © 2006 John Wiley & Sons, Ltd.     

Immobilization of laccase onto poly(glycidylmethacrylate) brush grafted poly(hydroxyethylmethacrylate) films: Enzymatic oxidation of phenolic compounds

Poly(hydroxyethylmethacrylate), p(HEMA) films were prepared via UV-initiated photo-polymerization. After activation of the hydroxyl groups of p(HEMA) by bromination, surface-initiated atom transfer radical polymerization (ATRP) of glycidylmethacrylate was conducted in dioxane/bipyridine mixture with CuBr as catalyst at 65 °C. The epoxy groups of the poly(glycidylmethacrylate) brushes were converted into amino groups with the reaction of ammonia. The modified p(HEMA-g-GMA)-NH₂ films were used as an ion-exchange support for the immobilization of laccase. The influence of pH and initial laccase concentration on the immobilization capacity of the p(HEMA-g-GMA)-NH₂ films has been investigated. The amount of immobilized laccase on the p(HEMA-g-GMA)-NH₂ films was determined as 139 μg/cm² films. The recovered activity of the immobilized laccase on the fibrous polymer grafted films was about 71% compared to free enzyme. The maximum activity (V_max) and Michealis constant (K_m) of laccase immobilized on the films, were found to be 15.4 U/mg and 23 mM, respectively. Finally, the immobilized laccase was operated in a batch system for enzymatic oxidation of phenol, p-chlorophenol and aniline.     

Electrical properties of thin PbTe films on Si substrates

An attempt was made to reduce the carrier concentration in thin PbTe films on Si substrates by optimizing deposition conditions. A modified hot-wall method was used for reproducible growth ofp-type films with 5 × 10¹⁵ < p(77 K) < 5 × 10¹⁷ cm^-3 andn-type films with 3 × 10¹⁵ < n(77 K) < 5 × 10¹⁶ cm^-3. The IR irradiation was found to have a significant effect on the temperature variation of film resistance. The activation energy of the IR-sensitivity centers was determined to be 0.11 ± 0.005 eV at room temperature and 0.18 ± 0.005 eV between 150 and 180 K.     

Structure and ferroelectric properties of stoichiometric and Sr-deficient–SrBi<Subscript>4</Subscript>Ti<Subscript>4</Subscript>O<Subscript>15</Subscript> thin films

SrBi₄Ti₄O₁₅ (SBTi) and Bi-excess and Sr-deficient SBTi (Sr-deficient SBTi, Sr_0.8Bi_4.13Ti₄O₁₅) thin films were deposited on Pt/Ti/SiO₂/Si (100) substrates using a sol–gel method. Structure and electric properties were investigated systematically. These films were random oriented. The remnant polarization (2P _r) of SBTi film was about 25.3 μC/cm², which was larger than the reported value of SBTi thin film. The film with Sr-deficient and Bi-excess composition showed a very large remnant polarization of 36.6 μC/cm². The capacitance–voltage (C–V) characteristics of both the films showed normal ferroelectric behavior. The Curie temperatures of the same Sr-deficient and Bi-excess component ceramics sample increased slightly in comparison with that of SBTi. More importantly, the Sr-deficient and Bi-excess SBTi thin film showed high fatigue resistance against continuous switching up to 4.4 × 10¹⁰ cycles.     

Molecular imprinted particles for lysozyme purification

Molecular recognition-based separation techniques have received much attention in chemistry and biology because of their high selectivity for target molecules. The aim of this study is to prepare lysozyme-imprinted polymers which can be used for the purification of lysozyme from aqueous solutions and egg white. N-methacryloyl-(l)-histidinemethylester (MAH) was chosen as the metal-complexing monomer. In the first step, Cu²⁺ was complexed with MAH and the lysozyme-imprinted poly(HEMA–MAH) [Lys-MIP] particles were synthesized by UV-initiated bulk polymerization. After that, the template (i.e., lysozyme) were removed using 0.1 M NaCl solution. The specific surface area of the Lys-MIP particles was found to be 22.9 m²/g with a size range of 20–63 μm in diameter and the swelling ratio was 57%. According to the elemental analysis results, the particles contained 421 μmol MAH/g polymer. The maximum lysozyme adsorption capacity was 12.1 mg/g polymer. The relative selectivity coefficients of imprinted particles for lysozyme/human serum albumin and lysozyme/cytochrome c were 3.6 and 4.1 times greater than NIP particles, respectively. Purification of lysozyme from egg-white was also monitored by determining the lysozyme activity using Micrococcus lysodeikticus as substrate. The purity of the desorbed lysozyme was about 89% with recovery about 84%. The Lys-MIP particles could be used many times without decreasing their adsorption capacities significantly.     

Preparation of ferroelectric PZT films by thermal decomposition of organometallic compounds

Transparent PZT thin films with perovskite structure were successfully obtained by thermal decomposition of organometallic compounds at the temperatures of 500 to 700° C. The films deposited on platinum substrates were smooth and uniform, but microcrackings were observed in the films deposited on fused silica substrates. The ratio of metal composition in the PZT film agreed with that in the mixture of starting materials. Films obtained at 700° C on platinum substrate showed a hysteresis loop. A spontaneous polarization was 35.65μC cm⁻², a saturation remanent polarization was 30.56μC cm⁻² and a coercive field was 45 kV cm⁻¹. Dielectric constant and dielectric loss angle were about 300 and 0.05, respectively.     

Yttrium-substituted bismuth titanate (Bi4−x Y x Ti3O12) thin film for use in non-volatile memories

Fatigue-free Bi_3.2Y_0.8Ti₃O₁₂ (BYT) thin films were grown on Pt/TiO₂/SiO₂/Si substrates using direct liquid injection–metal organic chemical vapor deposition. The BYT film capacitor with top Au electrode showed higher remanent polarization (2P _r) and lower leakage current density compared with Bi_3.2La_0.8Ti₃O₁₂ (BLT) film capacitors. BYT films showed strong (1 1 7) orientation with smaller grain size, while BLT films showed strong c-axis orientation. The 2P _r value of the BYT capacitor was 15 C cm^–2 and remained essentially constant up to 1×10¹⁰ read/write switching cycles at a frequency of 1 MHz. The leakage current of the BYT film was 3.5×10^–7 A cm^–2 at an applied voltage of 2 V, which is about three orders lower than that of the BLT film.     

An Improved Procedure for Preparing Epitaxial Tl–2201 Films on Single Crystal LaAlO3 and SrTiO3

Epitaxial Tl-2201 films are prepared on single crystal LaAlO ₃ and SrTiO ₃ by thallization of thallium-free precursor films made by laser ablation. Thallization is carried out in two consecutive steps. In the first step, at 720 °C, a smooth and epitaxial film is produced. The second thallization, at 820 °C, improved film crystallinity and the T _c . The films were characterized by X-ray diffraction and by resistance and susceptibility measurements. For a film on single crystal LaAlO ₃ , the FWHM of the scan (0,0,10) was 0.27°. T _c was 84K while J _c , reached 1.6×10 ⁶ A/ cm ² at 77K. A film on single crystal SrTiO ₃ exhibited somewhat lower T _c (78 K) while J _c was much smaller (9.5×10 ³ A/cm ² at 70.4K).     

Structural and optical properties of sulfurized Cu2ZnSnS4 thin films from Cu–Zn–Sn alloy precursors

This study reports the preparation of Cu₂ZnSnS₄ (CZTS) thin films by magnetron sputtering deposition with a Cu–Zn–Sn ternary alloy target and sequential sulfurization. The effects of substrate temperatures on the structural, morphological, compositional as well as optical and electrical properties were characterized. The results showed the CZTS thin films prepared by sulfurization at substrate temperature of 570 °C yielded secondary phases along with CZTS compound. The relatively good properties of CZTS thin film were obtained after sulfurization at substrate temperature of 550 °C. This CZTS film showed compact structure with large grain size of 900 nm, direct optical band gap of 1.47 eV, optical absorption coefficient over 10⁴ cm^?1, resistivity of 4.05 Ω cm, carrier concentration of 8.22 × 10¹⁸ cm^?3, and mobility of 43.38 cm² V^?1 S^?1.     

Fracture behavior of nylon hybrid composites

Hybrid composite systems consisting of liquid crystalline polymer (LCP), short glass fibers and toughened nylon in varied ratios were studied. Dynamic mechanical results indicated that, elastomeric phase in toughened nylon 6,6 promoted a better compatibilization between nylon 6,6 and LCP in a hybrid system containing short glass fibers in comparison with one without glass fibers. Improved compatibility facilitated fibrillation of LCP phase in the skin region of the hybrid composite, thereby providing superior tensile strength. Without the presence of LCP, glass fiber reinforced toughened nylon 6,6 exhibited the least tensile strength. J-integral analysis and essential work of fracture (EWF) method were used to compare the fracture behavior of composites. Results showed that specific essential work of fracture were consistent with the critical J-integral. Matrices reinforced by LCP alone showed the best crack initiation and propagation toughnesses, followed by glass fiber reinforced and hybrid composites. The better compatibility between nylon 6,6 and LCP appeared to inhibit the interfacial debonding process, resulting in brittle fracture.     

Porous Ultrahigh Gas‐Permeable Polypropylene Film and Application in Controlling In‐pack Atmosphere for Asparagus

Porous polypropylene (PP) films with greater gas permeability and lower permeability ratios (β) than existing commercial films were developed for fresh produce packaging. PP containing high content of beta‐form crystal was biaxially stretched under controlled conditions. Resulting porous films with uniquely high oxygen transmission rate (OTR) of 2 659 000 cm³?m^?2?d^?1, water vapor transmission rate of 67 g?m^?2?d^?1, and β value of 0.76 was used as a “breathable window” attached to the less permeable commercial BOPP (biaxially oriented PP) lidding film. Various sizes/areas of the breathable windows were designed and tested on packaging asparagus of 400 g, at 5°C. Results demonstrated that in‐pack O₂ and CO₂ concentrations could be practically controlled and modified by changing areas of the breathable windows. Altered porous high OTR area directly affected total gas permeation of the package. Optimum gas composition of Ο₂ and CΟ₂ within the recommended controlled atmosphere for asparagus, stored at 5°C, was effectively created and maintained in the package containing 25 cm² breathable window (15% of total film lid's area). The shelf life of asparagus under optimum modified atmosphere was extended to 29 days, as compared with <3 days in the normal, low OTR tray sealed with BOPP lidding film. Clearly, these developed porous ultrahigh permeable PP films can be useful materials in designing high OTR package with desirable in‐pack O₂ and CO₂ concentrations. Copyright © 2013 John Wiley & Sons, Ltd.     

Ferroelectric polymeric PVDF films prepared by ultrasonic atomization method

Ferroelectric poly (vinylidene fluoride) (PVDF) films were prepared by ultrasonic atomization. Various thickness and surface morphology of PVDF films were obtained by changing the frequency of an ultrasonic atomizer. The films were characterized by atomic force microscope (AFM) and ferroelectric tester. The results showed that there were some improvements in the thickness control and surface smoothness of polymeric PVDF films, which are critical problems for film deposition such as solution casting method. Ferroelectric properties measurement indicated that the films after corona charging displayed typical ferroelectric P–E hysteresis loops, giving a remanent polarization, P _r, of 5 μC/cm² and coercive field, E _c, of 150 MV/m. The maximum film deposition rate was 85 nm/min at the frequency of 6 MHz.