Solution Casting Research Articles

Edible Films from the Laboratory to Industry: A Review of the Different Production Methods

AbstractEdible films or coatings as potential replacements for traditional plastic food packaging are a popular subject for research. This article provides a narrative summary of the progress of research into edible food packaging and preparation methods at three different production scales over the past 5 years. First, at the laboratory research level, commonly used coating methods include dipping, vacuum dipping, and spraying. Films are mostly made by solution casting, while 3D printing film technology and electrospinning/electrostatic spraying are emerging technologies in the field. At the pilot level, panning coating, brush coating, and fluidized bed technologies give edible food packaging a more scalable and realistic approach. On an industrial manufacturing scale, in order to improve film formation efficiency, blowing, injection, calendering, etc. are generally based on the extrusion mode. Laboratory-scale research is critical for developing materials and exploring their properties. The technology used for industrial-scale production needs to consider factors such as cost and efficiency. Each technology for making food packaging needs to be selected according to the production purposes and the currently available packaging equipment. However, commonly used edible packaging source materials are generally derived from biological macromolecules such as proteins and polysaccharides. These materials are heated and extruded in industrial production, and their performance will be inferior to that of traditional plastic packaging. In addition, high cost is also a factor that must be considered.

Fabrication and characterization of extracted microsized chitosan embedded PVDF membrane for wastewater treatment

Abstract Critical water crisis due to overpopulation, industrialization and urbanization has resulted to the shortfall of providing safe drinking water to one billion people in the world. This work intends to fabricate modified hydrophobic polyvinylidene fluoride (PVDF) membrane by hydrophilic chitosan extracted from waste fish scales for wastewater treatment. Chitosan was blended with PVDF in N-methyl-2-pyrrolidone solution by solution casting method. Three different concentrations of 1, 3 and 5 wt% of chitosan were taken. The morphological, spectral and thermal analysis of the produced films were elaborately studied. The contact angle decreased with the increase of chitosan content from 82.64° to 60.97°. The tensile strength decreases from 1.11 to 0.38 MPa and Young’s modulus decreased from 12.08 to 7.4 MPa with increase in chitosan content in the film from 1 to 3 %. The performance of microparticle embedded membrane was compared with the pristine PVDF membrane, and it was affirmed that the microsized-chitosan embedded PVDF membrane manifests a broad promising application perspective towards wastewater treatment owing to its excellent water flux (76 L m−2 h−1) as well as antibacterial properties.

Investigation of the Effects of Different Phases of TiO2 Nanoparticles on PVA Membranes

Introduction: PVA/TiO2 nanocomposite membranes are prepared by solution casting technique where different phases of TiO2 nanoparticles like brookite, brookiterutile and rutile are dispersed in PVA matrix. Sol-gel method was employed to prepare TiO2 nanoparticles, while different phases of TiO2 have been obtained by controlling the calcination temperature. Methods: PVA/TiO2 nanocomposite membranes were characterized by XRD, FTIR, AFM, TEM, UV-visible and PL techniques. XRD results confirmed the presence of different phases of TiO2, exhibiting 3.3 nm, 8.4 nm, and 35.7 nm mean crystalline size. The XRD studies also confirmed that TiO2 nanoparticles became properly dispersed to the PVA matrix, leading to increased PVA crystallinity after doping of different phases of TiO2 nanoparticles. UV-visible analysis revealed an increase in absorption intensity and peak position shifts slightly towards longer wavelengths, which indicates that nanofillers tuned the band gap of PVA. The doping of the TiO2 (brookite) phase in the PVA matrix results in a decreased in PL intensity. Results: This suggests that the PVA/TiO2 (brookite) membrane exhibits a greater degree of photocatalytic activity in comparison to the other two composites. According to the FTIR investigation, the hydroxyl (OH) groups present in PVA interact with the dopants Ti+ ions via intra- and intermolecular hydrogen bonds to produce charge transfer complexes (CTC). The AFM study shows surface roughness details for PVA and PVA/TiO2 composite membranes. The average grain size of TiO2 nanoparticles calculated from TEM images is in good agreement with the grain size calculated by XRD. Conclusion: By adjusting the phase of TiO2 nanoparticles into PVA matrix, composites can be developed that are optimized for a variety of applications such as water purification, UV protection, self-cleaning surfaces, lithium-ion batteries, and optoelectronic devices.

Characterization Bio-Based Edible Film from Mango Seed Starch and Semi-Refined Carrageenan (Euchema cottonii) Using Sorbitol Plasticizer for Potential Food Contact Materials

Meanwhile, Semi-Refined Carrageenan (SRC) could be combined with starch as the base material for edible film fabrication to increase its tensile strength. This study aimed to identify edible film by synthesizing SRC and mango seed starch with plasticizer sorbitol, which could be safe for consumption in food packaging. The process of making edible film consists of three steps: extracting Eucheuma cottonii seaweed, making starch from mango seeds, and making edible film. The method used was the solution casting method, with a ratio of SRC: starch of mango seeds, namely 1: 0; 0.7: 0.3; and 0: 1 (w / w) and sorbitol concentrations of 20, 30, 40, 50, and 60% (w/w). This research shows that increasing sorbitol could decrease the tensile strength but increase the elongation and solubility of the edible film. As well as the combination of SRC and mango seed starch can produce edible films with higher characteristics than edible films based only on SRC or mango seed starch. The results of selecting the best conditions for an edible film based on the Japanese Industrial Standard (JIS) are the concentration ratio of SRC: mango seed starch (0.7: 0.3) and 30% sorbitol concentration with a thickness value of 0.22 mm, tensile strength 4.81 MPa, 28.50% elongation and 68.44% solubility

Investigation of Optical and Dielectric properties of Mg(ClO4)2 based PVC+ZnO Nanocomposite Polymer Electrolytes

Nanocompistie polymer electrolytes of PVC+ZnO+Mg(ClO4)2 were synthesized by solution casting and studied using UV-visible spectroscopy and AC conductivity. The electrolytes had varying amounts of Mg(ClO4)2. Based on the findings of the UV visible spectroscopy, the sample with x=50 wt.% Mg(ClO4)2 had the best direct and indirect band gap values, suggesting that the interaction between the polymer, ZnO nanofiller, and Mg(ClO4)2 salt improved its optical properties. In terms of dielectric constant and ion dissociation, the sample with x=75 wt.% Mg(ClO4)2 performed the best out of all of the samples tested. polymer electrolyte with frequency- dependently high dielectric constant values is perfect for cutting-edge applications. Key words: polymer electrolyte, solution casting, UV -visible spectroscopy, AC conductivity, dielectric constant.

Modification of opto‐electrical behavior of polyvinyl chloride by infusion of SrTiO3 nanofiller synthesized via green route

AbstractEnhancing the opto‐electrical properties of polymer is crucial for optoelectronic devices. This study emphasis the synthesis of strontium titanate (SrTiO3) nanoparticles using a green sol–gel method and incorporates them into polyvinyl chloride (PVC) to create nanocomposite films via solution casting. The structural, optical, thermal, and electrical properties of PVC with SrTiO3 at concentrations of 1, 3, and 5 wt.% were examined. Better crystallinity was obtained with filler incorporation. Fourier transform infrared shows the physical interaction between nanofiller and the matrix. SEM results suggested that SrTiO3 nanofiller are well distributed in PVC surface. UV–Vis spectroscopy was used to study optical behavior of the nanocomposites. Optical bandgap energy decreased from 3.2 to 2.5 eV with increased concentration of SrTiO3 in PVC matrix. Photoluminescence results show the reduction of electron hole recombination rate. The integration of SrTiO3 nanofiller into the PVC matrix improved the thermal stability, dielectric constant, and the overall performance of the prepared nanocomposite films, making them suitable for high‐temperature optoelectronic and energy storage applications. The green synthesis of SrTiO3 nanofiller also ensures the environmental benefits, high purity, and homogeneity, leading to consistent enhancements in the PVC/SrTiO3 composites. These improvements highlight their potential for advanced optoelectronic devices requiring efficient and durable materials.

Tamarind gum based magnesium ion conducting polymer membrane for energy storage applications

A solid bio polymer electrolyte (SPE) based on tamarind gum (TG) and magnesium nitrate was synthesized by a solution casting technique. The amorphous behavior is observed by X-ray diffraction (XRD) analysis, and the degree of crystallinity is calculated from the XRD deconvolution spectra. The interaction between the polymer and the salt was confirmed by Fourier transform infrared (FTIR) analysis. Using FTIR deconvolution spectra, the percentage of free ions can be calculated. The glass transition temperature (Tg) was determined via differential scanning calorimetry (DSC). A higher ionic conductivity (σ) of 1.97 × 10−4 S/cm is observed for the sample with 1 g of tamarind gum and 0.5 g of magnesium nitrate (4 TMN). The conduction mechanism shows that sample 4 TMN obeys the quantum mechanical tunneling model (QMT) at low frequency. The prepared SPEs follow the Arrhenius behavior, and the minimum activation energy (Ea) of 0.207 eV is observed for sample 4 TMN. The lowest relaxation time (τ) was 3.46 × 10−7 s for 4-TMN according to the tangent spectra. The transference number of ions (tion) is calculated by Wagner’s polarization method. The electrochemical stability window observed by linear sweep voltammetry (LSV) is 2.25 V. The primary battery is fabricated by using sample 4TMN, and an open circuit voltage (OCV) of 2.01 V is observed.

Investigation of Structural and Thermal Properties of Mg(ClO4)2 Based PVC + ZnO Nanocomposite Polymer Electrolytes

PVC+ZnO+Mg(ClO4)2 nanocompistie polymer electrolyte of differnet concentrations of Mg(ClO4)2 electrolytes were prepared using solution casting technique and further characterized using XRD, FTIR and TGA & DTA. The results of XRD suggests that the high amorphous of the PVC/ZnO nanocomposite with x=50 wt.% Mg(ClO4)2. As it due to high amorphous nature it can show a good ionic conductivity. The FTIR peaks shifting may also representing change of bond length and attaining good amorphous nature. The high heat resistance for all the sample can notice for DGA-DTA. Key word: polymer electrolyte, XRD, FTIR, TGA & DTA, Nanofiller

Na3Zr2Si2PO12-Polymer Composite Electrolyte for Solid State Sodium Batteries.

The integration of the flexibility of organic polymer electrolyte and high ionic conductivity of the ceramic electrolyte is attempted in search of efficient and safer battery. Composite solid polymer electrolyte (CSPE) provides high ionic conductivity with a sustainable thin film of electrolyte having the synergistic effect of ionic liquid and active inorganic filler. The CSPE is synthesized by the solution cast technique using Na3Zr2Si2PO12 (NZSP) as ceramic and poly(vinylidene fluoride-hexafluoropropylene) with Salt-Ionic liquid as polymer electrolyte. X-ray diffraction (XRD) of CSPE includes amorphous nature due to the polymer part as well as crystalline peaks of ceramic NZSP, simultaneously. The prepared CSPE sample shows homogeneous and interconnected surface morphology is observed by Scanning electron microscopy (SEM) image. Thermogravimetric analysis (TGA) shows electrolyte is thermally stable up to 200 °C and differential scanning calorimetry (DSC) reveals decrease in degree of crystallinity due to NZSP addition in the CSPE. By complex impedance spectroscopy (CIS), room temperature ionic conductivity of the prepared CSPE is found ~1.03 mS/cm. The dielectric behaviour of the prepared electrolyte is also studied to investigate the ion dynamics within the sample. The cationic transference number is 0.53 and the electrochemical stability window (ESW) of the CSPE is 4.9 V which is suitable for sodium solid-state batteries applications.

Characterization of anti bacterial biocomposite films based on poly lactic acid and prosopis juliflora bark powder

Biocomposites can be a solution for environmental pollution and sustainability by acting as an alternative to petroleum-based products used in the field of packaging and biomedical applications. Herein, an attempt to valorize the potential of Prosopis juliflora plant to fabricate Polylactic acid (PLA) based biocomposites. The biocomposites comprised of Prosopis juliflora bark powder (PJBP) and PLA were fabricated by solution casting method with various weight percentages (Wt%) of PJBP. PJBP/PLA films show uniform functional group interactions through FTIR analysis. The 25 % PJBP/ PLA biocomposite shows the highest crystalline size of 8.9 nm. The 25 wt% included PJBP increases the thermal stability by 6.9 %, surface roughness by 212 %, and tensile strength by 45.5 % compared to PLA film. The 25 % PJBP film shows increment in the water absorption and water vapor permeability test. In addition, the antibacterial behavior of 25 % PJBP bio composite shows higher inhibition zones against the gram-positive and gram-negative pathogens. Biocomposite films with PJBP content show 40 % degradation in soil for degradation analysis. This PLA/25 % PJBP biodegradable film can be used as an alternative for petroleum-based products in the field of packaging as well as the biomedical field.

Chemoselective modification of chitosan with arginine and hydroxyproline: Development of antibacterial composite films for wound healing applications

This study explored the enhancement of chitosan for wound dressing applications through selective functionalization with arginine and hydroxyproline amino acids, combined with polyvinyl pyrrolidone (PVP) and polyvinyl alcohol (PVA) in composite films. The research employed chemoselective amino acid grafting followed by solution casting to fabricate the composite materials. Fourier transform infrared (FTIR) analysis verified successful chitosan modification through the presence of a carbamate bond at 1719 cm−1 and an amide bond shift from 1660 to 1680 cm−1, with nuclear magnetic resonance (NMR) analysis providing additional confirmation. The composite films demonstrated exceptional properties, achieving maximum tensile strength of approximately 55 MPa and swelling ratio of about 400 %. Statistical analysis revealed significant variations in mechanical and swelling properties across formulations (p < 0.05), with analysis of variance (ANOVA) showing a between-group sum of squares of 122,980.519 for tensile strength and 352,306.333 for swelling. Duncan's multiple range test identified distinct groupings for tensile strength (5.67–119.67 MPa) and swelling ratios (320.33–565.33 %), demonstrating the impact of composition on material properties. Thermal stability analysis (25–600 °C) revealed a multi-step degradation process, confirming successful modification and composite formation. The amino acid-modified chitosan composites showed remarkable antibacterial enhancement, exhibiting 60 % greater activity against both Gram-positive and Gram-negative bacteria compared to unmodified chitosan. These findings demonstrate the potential of selectively functionalized chitosan composite films for advanced wound dressing applications, combining enhanced antibacterial efficacy with robust mechanical and thermal properties. Future research directions include formulation optimization and in vivo validation of clinical efficacy.

Induced Electron Traps via the PCBM in P(VDF-HFP) Composites to Enhance Dielectric and Energy Storage Performance

Polymer-based composites with excellent dielectric properties are essential for advanced energy storage applications. In this work, the [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) as a filler was incorporated into the poly(vinylidene fluoride-co-hexafluoropropylene) (P(VDF-HFP)) composite to improve its dielectric performance. P(VDF-HFP) composite films with varying PCBM concentrations were prepared via solution casting and their dielectric, energy storage, and charge–discharge properties were characterized. It was found that the doped PCBM could introduce new charge traps with an energy level of 1.25 eV that modulate charge transport and energy storage characteristics of the polymer matrix. The dielectric constant of the composites was enhanced to the maximum of 10.87 as 0.2 vol% PCBM was added, while the breakdown strength reached 455 MV/m, achieving an energy density of 7.38 J/cm3, which is 33% higher than the pristine P(VDF-HFP) film. Furthermore, the charge–discharge efficiency of the composites was enhanced 66% under the electric field of 300 MV/m. These results demonstrate that PCBM significantly improves the dielectric and energy storage properties of P(VDF-HFP) composites, providing a promising approach for the development of high-performance dielectric materials in flexible energy storage devices.

Copper Acetate Monohydrate/Nickel Chloride Impregnated PVDF Ultrafiltration Membrane: An Antifouling Membrane for Peat Water Treatment

AbstractThis study examines the polyvinylidene fluoride (PVDF) ultrafiltration membrane impregnated with the copper acetate monohydrate/nickel chloride/thiourea (CuNit) nanoparticle through its physical properties, chemical properties, water flux, humic rejection, and antifouling properties against peat water. The ultrafiltration membrane was fabricated via phase inversion by blending CuNit nanoparticles (1, 3, and 5 wt/wt PVDF %) and PVDF (16 wt %) in N‐Methyl‐2‐pyrrolidone (NMP, 42 wt %) as the solvent. The humic rejection and fouling test are conducted using peat water collected from the Beladin water treatment plant. As a result, M03, which has 1 wt/wt PVDF % of CuNit nanoparticle, gives a better result of pure water flux, humic rejection, and fouling recovery rate with a value of 82 L/m2 h, 93 %, and 40 % compared to pristine PVDF membrane. The fouling of M03 recorded a low total rate of fouling (76 %) that is caused by high reversible fouling and low irreversible fouling with a value of 0.16 and 0.59, respectively, compared to the pristine PVDF membrane. In conclusion, due to the agglomeration that occurs in the further addition of CuNit nanoparticles, coating or encapsulation must be done to improve the stability of nanoparticles and reduce the leach‐out problem as well as provide a good distribution between the nanoparticle and casting solution during the membrane fabrication.

Novel visible-light-driven antibacterial film grafted with 3,3,4,4-benzophenone tetracarboxylic acid (BPTCA) for chilled meats preservation

To improve long-term stability and low-toxicity active packaging systems, three visible-light-driven antibacterial packaging films from chitosan (CS), silk fibroin (SF), polyvinyl alcohol (PVA) and 3,3,4,4-benzophenone tetracarboxylic acid (BPTCA) were fabricated in this study. First, CS/PVA, SF/PVA and CS/SF/PVA films by solution casting method, and enhance their water solubility by glutaraldehyde (GA) cross-linking to obtain CS/PVA-G, SF/PVA-G and CS/SF/PVA-G. Then, BPTCA was covalently immobilized onto CS/PVA-G, SF/PVA-G and CS/SF/PVA-G through the esterification to obtain CS/PVA-B, SF/PVA-B and CS/SF/PVA-B, respectively. The chemical structure, photophysical properties, and antibacterial capacities are characterized. The FTIR revealed that BPTCA is covalently grafted with the polymer matrix via ester bond. Furthermore, grafting of BPTCA enhanced the film's UV-blocking, decreased water contact angle, water vapor permeability, and possessed moderate mechanical properties. Meanwhile, CS/SF/PVA-B has the best reactive oxygen species generation ability and antibacterial activity (against Escherichia coli, Staphylococcus aureus, Salmonella enteritidis), and can recycle four times, overall migration value of BPTCA was within the limits of 10 mg/dm2. We apply CS/SF/PVA-B films combined with palletized packaging to different chilled-meat preservation applications, and measure physicochemical changes and microbial counts. Shelf lives of chilled mutton are extended by 3 d and chicken by 6 d, compared with controls without CS/SF/PVA-B film. A covalent immobilized visible-light-driven antibacterial packaging may improve the long-term quality of chilled meats.

MgO nanofiller reinforced biodegradable, flexible, tunable energy gap HPMC polymer composites for eco-friendly electronic applications

This study explores the development and characterization of eco-friendly Magnesium Oxide (MgO) nanofiller reinforced hydroxypropyl methylcellulose (HPMC) polymer composites for eco-friendly electronic applications. The prepared nanocomposites are biodegradable and flexible without any additional plasticizer. MgO nanoparticles were synthesized using the solution combustion method and incorporated into HPMC matrix through solution casting method. The structural, mechanical, optical, AC and DC electrical, and degradation properties of the prepared nanocomposites were systematically investigated. X-ray diffraction (XRD) confirmed the successful integration of MgO nanoparticles into the HPMC matrix, with noticeable interactions affecting the crystallinity. Mechanical testing revealed an optimal MgO concentration of 0.2 g, which provided the best balance of strength and ductility, while higher concentrations led to increased brittleness. UV–Vis spectroscopy results evident that the energy gap of nanocomposites can be tuneable with MgO incorporation. The photoresponsivity study indicated that higher MgO content reduce the photocurrent due to agglomeration and defect states. Dielectric studies showed a typical frequency-dependent behaviour, with enhanced dielectric constants at lower frequencies attributed to interfacial polarization. However, increasing MgO content decreased the dielectric constant and loss due to reduced polymer chain mobility and increased resistive pathways. Current-Voltage (I-V) characteristics demonstrated a non-ohmic conduction behaviour with Poole-Frenkel emission identified as the predominant conduction mechanism. Degradation tests in both tap water and soil, demonstrated that the MgO incorporation significantly slowed the degradation rate of the composites, enhancing their durability. These findings suggest that MgO-HPMC nanocomposites hold promise for sustainable and flexible eco-friendly electronic applications.

Synthesis of a gallic acid-based self-healing waterborne polyurethane with a thermo-responsive dynamic phenol-carbamate network for enhanced mechanical strength, antimicrobial activity, and shape memory properties

To expedite the advancement of multifunctional next-generation smart materials, it is imperative to create polymers derived from renewable, green bio-based resources. This paper presents a direct synthesis of thermo-responsive aqueous polyurethanes by combining gallic acid (GA) with isocyanate groups to form a dynamic phenol-carbamate crosslinked network and the incorporation of the metal-organic framework Cu-MOF-2 for synergistic effects. The resulting GA-based polyurethane (MOF-GWPU) exhibits excellent thermal stability and mechanical properties, achieving an ideal balance between mechanical strength and self-healing efficiency. The MOF-GWPU film demonstrates strong antimicrobial efficacy against Escherichia coli and Staphylococcus aureus, highlighting its exceptional antibacterial performance. The thermo-responsive dynamic covalent bonds enable the MOF-GWPU film to rapidly revert from a temporary shape back to its original form. Post-processing experiments further indicate that the crosslinked GA-PU polymer can be efficiently recycled through solution casting and hot-pressing techniques. This design offers a novel approach and valuable insights for advancing the development of multifunctional smart polymers derived from bio-based resources.

Ionic liquid/polybenzimidazole/SiO2 composite membranes for medium temperature operating

Fuel cells (FC) with proton exchange membranes (PEMs) are seen as an alternative energy source due to their efficiency, power density, low emissions, and reliable energy supply. Proton exchange membranes based on polybenzimidazole have shown potential for operating at high and medium temperatures to enhance FCs performance. New composite membranes made from m-PBI and diethylammonium mesylate [DEAH/MsO] ionic liquid were prepared trough a solution casting method. Silica nanopowder (SiO2) was used as an inorganic filler at varying concentrations (0.5–20 wt%). The ionic liquid content in the membranes ranged from 1 to 2.5 mol per mole of PBI monomer units. Our study is focused on the thermal properties, such as thermal stability and phase transition temperatures, morphology, conductivity, and electrochemical stability of the membranes. The influence of the inorganic filler on these properties was also discussed.

Robust self-healing capacity and high mechanical properties of castor oil-based waterborne polyurethane based on “kill two birds with one stone” strategy

Achieving ideal combination of high self-healing efficiency and good mechanical properties is of significance for the breakthrough in the application of self-healing materials. Herein, the functionalized castor oil-based waterborne polyurethane (DA-CWPU) was constructed based on “killing two birds with one stone” molecular design strategy with the addition of self-healing monomer D-A adduct. Firstly, D-A adduct containing flexible D-A bonds and rigid ring structure was prepared by D-A reaction with furfuryl alcohol (FA) and bismaleimide (BMI) as raw materials, which could not only effectively enhanced the self-healing ability of the material, but also ensured the strong mechanical properties. Then, DA-CWPU emulsion with favourable self-healing and mechanical properties was synthesized by the polymerization of castor oil (CO), isophorone diisocyanate (IPDI) and D-A adduct. The DA-CWPU film has preferable self-healing efficiency (93 % at 100 °C for 50 min), unique shape memory effect (rehabilitate after heating at 100 °C for 45 s), good toughness (485 MJ/m3), strong tensile strength (5.96 MPa) and sufficient elongation (115 %). At the same time, the self-healing DA-CWPU film can be recycled through solution casting. The sustainable castor oil-based waterborne polyurethane can be used as finishing agents for leather products, which realizes repeatedly self-healing in case of surface damage, greatly increasing the service life of the material and mechanical properties, providing a new approach for the development of mechanically robust self-healing materials.

Physicochemical and biological evaluation of ‘click’ synthesized vinyl epoxide-chitosan film for active food packaging

Chitosan (Cs) being a natural biopolymer serves as an excellent template to construct active packaging materials for achieving sustainable development. In this study, Cs was chemically modified via epoxide ring opening click reaction using vinyl epoxide to obtain a novel chitosan vinyl epoxide (Cs-VE) derivative with hydroxyl and olefinic functional groups. The Cs-VE transparent film was fabricated through the eco-friendly solution casting technique. A meticulous investigation into the chemical structure and physicochemical properties of the synthesized films was conducted using FT-IR, 1H NMR and XRD analyses. The thermal stability and homogeneity of the film were verified by thermogram and FE-SEM images respectively. Improved mechanical properties (tensile strength of 24.64 MPa and 12.08 % elongation at break) and excellent UV-light blocking ability (9.3 % transmittance at 350 nm and 22.15 % transparency at 600 nm) were observed. Also, important parameters such as water vapor permeability (WVP), swelling degree, water solubility and UV-barrier properties were found to be adequate for food packaging application. Similarly, enhanced antioxidant activity with 27.2 % and 73.6 % radical scavenging against DPPH and ABTS radicals respectively was observed for the synthesized Cs-VE film. The film showed antimicrobial activity against both bacteria and fungi. These results along with food packaging studies on Grewia asiatica fruit established the developed Cs-VE film as a suitable candidate for active food packaging application.

Preparation and Characterization of Tensile Properties of PMMA/SiC Nanowhiskers Nanocomposite Films: Effect of Filler Loading and Silane Treatment

The preparation of nanocomposites through melt mixing was challenging as the nanofillers tend to form agglomeration. The silicon carbide nanowhiskers (SiCNWs) filled poly (methyl methacrylate) (PMMA) thin film in this study was prepared by means of solution casting. Acetone with low toxicity was used as solvent to dissolve the PMMA pellets. A coupling agent, silane was used to enhance the properties of composite films. Besides, the untreated and treated SiCNWs were filled into PMMA matrix, respectively with the filler loading varied from 0.2 to 0.8 wt%. The universal testing machine was used to investigate the tensile properties of composites. It was found out that the tensile strength of the PMMA was reduced in the presence of SiCNWs. However, the tensile strength had increased with the rise of filler loading. At 0.8 wt% of SiCNWs, the composites’ tensile strength was comparable to virgin PMMA. Meanwhile, the SiCNWs had reduced the elongation at break but increased the elastic modulus of PMMA/SiCNWs nanocomposite films. In addition, silane surface treatment on SiCNWs had improved the tensile strength and ductility but lowered the elastic modulus of the nanocomposites. The improvement was due to the enhancement of interfacial adhesion between SiCNWs and PMMA.