Studies on the thermal and mechanical behavior of PLA‐PET blends

The increasing use of bio‐sourced and biodegradable polymers such as poly(lactic acid) (PLA) in bottle packaging presents an increasing challenge to the polyethylene terephthalate (PET) recycling process. Despite advanced separation technologies to remove PLA from PET recyclate, PLA may still be found in rPET process streams. This study explores the effects of PLA on the mechanical properties and crystallization behavior of blends of PET containing 0.5–20% PLA produced by injection molding. SEM indicates an immiscible blend of the two polymers and TGA confirms the independent behavior of the two polymers under thermal degradation conditions. Temperature‐modulated DSC studies indicate that adding PLA to PET increases the rigid amorphous fraction of the PET moiety. Critical amounts of PLA induce stress oscillation behavior during mechanical testing. The mechanical behavior of the samples is explained by antagonistic interaction between increased rigid amorphous fraction and decreased fracture strength arising from an increased population of PLA microparticles. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44147.     

Combined effect of a plasticizer and carvacrol and thymol on the mechanical,thermal, morphological properties of poly(lactic acid)

In this study, the effects of the monotherpenic phenol concentration on the properties of biocomposites containing plasticized poly(lactic acid) (PLA) with acetyl tributyl citrate (ATBC) were investigated. The monotherpenic phenols carvacrol (C) and thymol (T) were added to PLA by a melt‐blending method. The prepared samples were characterized by means of tensile testing, Fourier transform infrared spectroscopy, thermogravimetric analysis, differential scanning calorimetry, scanning electron microscopy (SEM), and antibacterial activity tests. The addition of ATBC to PLA resulted in hydrogen bonding between ATBC and PLA. We observed that ATBC, C, and T reduced the glass‐transition temperature of PLA. The presence of C and T decreased the maximum degradation temperature slightly. Because of the plasticization effect of the additives, the tensile strength and Young's modulus of PLA decreased, whereas the extent of elongation they experienced before failure increased. This effect was also observed with SEM analysis in terms of plastic deformation at break. The antibacterial activity tests showed that samples containing high concentrations of C demonstrated an improved antibacterial activity against Staphylococcus aureus, Salmonella typhimurium, and Listeria monocytogenes bacteria. We observed that C exhibited a higher inhibition against bacterial strains than T. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45895.     

Synthesis,characterization, and polymerization of a novel benzoxazine based on diethyltoluenediamine

A novel aromatic diamine‐based benzoxazine monomer (PDETDA) was successfully prepared from diethyltoluenediamine (DETDA), phenol, and paraformaldehyde through a simple one‐step solvent‐less method. The structure of PDETDA was confirmed by FTIR, ¹H NMR, and ¹³C NMR. The curing behavior of PDETDA was studied by DSC, FTIR, and rheological measurement. The results showed that the alkyl substituents on the benzene ring in DETDA not only facilitated the synthesis of PDETDA by effectively hindering the formation of triazine network, but also endowed PDETDA with the advantage of low viscosity (1 Pa s at 90°C). However, steric hindrance of the substituents made PDETDA difficult to form a crosslinked network through ring‐opening polymerization, and therefore only oligomers and noncrosslinked polymers were obtained. The curing kinetics of PDETDA was studied by nonisothermal DSC, and the results revealed that the curing of PDETDA displayed autocatalytic characteristic. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41920.     

Synthesis,characterization, and properties of cashew gum graft poly(acrylamide)/magnetite nanocomposites

Graft copolymer nanocomposites based on cashew gum and poly(acrylamide) with different concentrations of nano‐iron‐oxide particles (Fe₃O₄) have been prepared by an in situ polymerization method. The characterization of graft copolymer composite was carried out by FTIR, UV, XRD, SEM, DSC, and TGA, electrical conductivity, and magnetic property [vibrational sample magnetometer (VSM)] measurements. The shift in the spectrum of UV and FTIR peaks shows the intermolecular interaction between metal oxide nanoparticles and the graft copolymer system. The spherically shaped particles observed from the SEM images clearly indicating the uniform dispersion of nanoparticles within the graft copolymer chain. The XRD studies revealed that the amorphous nature of the graft copolymer decreases by the addition of Fe₃O₄ nanoparticles. The glass transition temperature studied from DSC increases with increase in concentration of metal oxide nanoparticles. Thermal stability of composite was higher than the pure graft copolymer and thermal stability increases with increase in content of nanoparticles. Electrical properties such as AC conductivity and dielectric properties of the composites increased with increase in concentration of metal oxide nanoparticles. The magnetic property of graft copolymer nanocomposites shows ferromagnetic and supermagnetism and the saturation of magnetism linearly increased with increasing the Fe₃O₄ content in the polymer composite. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43496.     

Thermally activated polymerization behavior of bisphenol‐S/methylamine‐based benzoxazine

A bifunctional benzoxazine monomer, 6,6′‐bis(3‐methyl‐3,4‐dihydro‐2H‐benzo[e] [1,3]oxazinyl) sulfone (BS‐m), was synthesized from bisphenol‐S, methylamine, and formaldehyde via a solution method. The chemical structure of BS‐m was characterized with ¹H and ¹³C‐nuclear magnetic resonance (NMR) spectroscopy, Fourier transform infrared (FTIR) spectroscopy, and elemental analysis. The ring‐opening polymerization reaction of BS‐m monomer was studied by FTIR, ¹³C solid‐state NMR, and differential scanning calorimetry. With the polymerization reaction proceeding, the intensities of the FTIR absorption peaks of CH₂, C? O? C, and C? N? C of the oxazine ring decreased gradually, and some of these absorption peaks disappeared. The shapes and intensities of the absorption peaks associated with benzene ring, sulfone group, and aromatic C? S bond changed in various ways. The changes in the solid‐state ¹³C‐NMR pattern, including chemical shifts, intensity of resonances, and line‐width, were observed from the spectra of BS‐m and the corresponding polybenzoxazine. The melting process of BS‐m overlapped with the beginning of the ring‐opening polymerization reaction. The polymerization kinetic parameters were evaluated for nonisothermal and isothermal polymerization of BS‐m. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Thermal properties of nanocellulose-reinforced composites: A review

Nanocellulose has received increasing attention in science and industry in recent years as a nanoscale material for the reinforcement of polymer matrix composites due to its superior mechanical properties, renewability, and biodegradability. New nanocellulose sources, modifications, and treatments are under development to reduce the high energy required during production and to create a more suitable industrial-scale production process. Thus, this paper reviews plant-based nanocellulose composites and their properties, with a focus on their thermal-related characteristics. The purpose of this review is to establish for readers the impact of the incorporation of nanocellulose on the thermal and dynamic mechanical properties of nanocellulose composites. Understanding of the thermal properties is important for researchers to assess the suitability of the nanocomposites for a variety of applications in response to new and evolving societal requirements. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48544.     

Synthesis and characterization of PLA nanocomposites containing nanosilica modified with different organosilanes II: Effect of the organosilanes on the properties of nanocomposites: Thermal characterization

Thermal behavior of polylactic acid (PLA)/nanosilica nanocomposites prepared via bulk ring opening polymerization from lactide was investigated by differential scanning calorimetry and thermogravimetric analysis (TGA). Both unmodified nanosilica and modified by surface treatments with different amounts of two distinct silanes were used. Samples containing pure silica show enhanced crystallization processes; with silane‐modified silica this effect is magnified, especially in the case of materials with high loadings of epoxy silane. Nonisothermal crystallization temperatures become higher and isothermal crystallization kinetics show a marked increase of Kinetic constant (K_c). TGA analyses show that, when pure nanosilica is present, nanocomposites have a thermal stability far greater than the one of standard PLA, starting their degradation at temperatures up to 70°C higher than the ones of pure PLA. When silanes are present, thermal stability lowers as silane content increases, but it is anyway higher than the one of the pure polymer. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Preparation and performance analysis of barium titanate incorporated in corn starch‐based polymer electrolytes for electric double layer capacitor application

Polymer electrolyte membranes composing of corn starch as host polymer, lithium perchlorate (LiClO₄) as salt, and barium titanate (BaTiO₃) as composite filler are prepared using solution casting technique. Ionic conductivity is enhanced on addition of BaTiO₃ by reducing the crystallinity and increasing the amorphous phase content of the polymer electrolyte. The highest ionic conductivity of 1.28 × 10^?2 S cm^?1 is obtained for 10 wt % BaTiO₃ filler in corn starch‐LiClO₄ polymer electrolytes at 75°C. Glass transition temperature (T_g) of polymer electrolytes decreases as the amount of BaTiO₃ filler is increased, as observed in differential scanning calorimetry analysis. Scanning electron microscopy and thermogravimetric analysis are employed to characterize surface morphological and thermal properties of BaTiO₃‐based composite polymer electrolytes. The electrochemical properties of the electric double‐layer capacitor fabricating using the highest ionic conductivity polymer electrolytes is investigated using cyclic voltammetry and charge‐discharge analysis. The discharge capacitance obtained is 16.22 F g^?1. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43275.     

Cross-linked poly(benzoxazole-co-siloxane) networks with high thermal stability and low dielectric constant based on a new ortho-amide functional benzoxazine

In this study, an amide functionalized bis-benzoxazine (AI-al) has been synthesized using allylamine, ortho-amide functional bis-phenol and paraformaldehyde as raw materials via Mannich condensation. This newly obtained benzoxazine has been used to react with polydimethylsiloxane (PDMS) through hydrosilylation to form poly(benzoxazine-co-amide-co-siloxane) (AI-al-PDMS) featuring siloxane, amide and benzoxazine as repeating units. The chemical structures of both oxazine ring-containing monomer and copolymer are confirmed by NMR and FT-IR spectroscopies. Besides, the thermally activated polymerization behaviors of AI-al and AI-al-PDMS are investigated by DSC, and the subsequent conversion of benzoxazole formation is studied by in situ FT-IR. Moreover, dynamic mechanical analysis and thermogravimetric analysis are used to determine the thermal properties of the cross-linked polymers. The resulting cross-linked poly(benzoxazole-co-siloxane) derived from AI-al-PDMS shows excellent thermal stability (no T_g can be observed before 400°C; Td5 of 393°C) and low dielectric constants (2.52–2.13 in the frequency range of 1 Hz to 1 MHz), evidencing its great potential applications in electronic packing, aerospace, and other high-performance fields.     

Degradation of PLA and PLA in composites with triacetin and buriti fiber after 600 days in a simulated marine environment

Poly(lactic acid) (PLA), the polymer object of this study, degrades by a biotic process after an abiotic hydrolysis process. Its degradation was evaluated after 600 days of exposure in a simulated marine environment (SME), as buriti fiber‐reinforced composites having triacetin as coupling agent. Composites were obtained by extrusion and films were produced by compression molding. After between 60 and 600 days of exposure, PLA had a weight loss of 2.5%, PLA/T of 1.5%, and 10–12% of weight loss for PLA/B and PLA/B/T, respectively. PLA intercalates reduction, increase, and decrease of its crystallinity attributed to hydrolysis (up to 15 days), impairment of amorphous segments (45 days), and loss of integrity of the matrix (100–600 days), respectively. In the PLA/T composites, triacetin inhibited the diatom colonization process, having its crystallinity values increased after nearly 100 days of exposure with subsequent reduction. For samples with buriti fiber, changes in crystallinity were attributed to absorption of water and exposure of matrix amorphous segments. PLA degradation in a SME is evidently favored by the use of natural fibers since they make easier water access to the matrix and colonization by the protists group, diatoms, showing that the polymer can have reduced post‐use shelf life as composites, with benefits while in use and at the same time post‐use environmental benefits. Triacetin inhibits PLA colonization and degradation up to 45 days after exposure, after which it no longer influences the degradation process. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43290.     

Preparation and properties of dopamine reduced graphene oxide and its composites of epoxy

To improve the thermal and mechanical properties and further to expand its applications of epoxy in electronic packaging, reduced graphene oxide/epoxy composites have been successfully prepared, in which dopamine (DA) was used as reducing agent and modifier for graphene oxide (GO) to avoid the environmentally harmful reducing agents and address the problem of aggregation of graphene in composites. Further studies revealed that DA could effectively eliminate the labile oxygen functionality of GO and generate polydopamine functionalized graphene oxide (PDA‐GO) because DA would be oxidated and undergo the rearrangement and intermolecular cross‐linking reaction to produce polydopamine (PDA), which would improve the interfacial adhesion between GO and epoxy, and further be beneficial for the homogenous dispersion of GO in epoxy matrix. The effect of PDA‐GO on the thermal and mechanical properties of PDA‐GO/epoxy composites was also investigated, and the incorporation of PDA‐GO could increase the thermal conductivity, storage modulus, glass transition (T_g), and dielectric constant of epoxy. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39754.     

Photocrosslinked biobased phase change material for thermal energy storage

A series of novel photocrosslinked biobased shape‐stabilized phase change materials (PCMs) based on octadecanol, eicosanol and docosanol have been prepared by UV technique for the purpose of thermal energy storage applications. Epoxidized soybean oil was reacted with acrylic acid to form acrylated soybean oil (ASO). The structure and composition, cross‐section morphology, thermal stability performances and phase change behaviors of ASO and UV‐cured PCMs were examined by using Attenuated total reflection fourier transform infrared spectroscopy, thermogravimetric analysis system (TGA), scanning electron microscopy, and differential scanning calorimetry. The results indicate that the UV‐cured biobased PCMs possess perfect phase change properties and a suitable working temperature range. The heating process phase change enthalpy is measured between 30 and 68 J/g, and the freezing process phase change enthalpy is found between 18 and 70 J/g. The decomposition of UV‐cured PCMs started at 260 °C and reached a maximum of 430 °C. All the biobased UV‐cured PCMs improved latent heat storage capacity in comparison with the pristine ASO sample. With the obtained results we conclude that, these materials promise a great potential in thermal energy storage applications. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43757.     

Preparation of alginate flame retardant containing P and Si and its flame retardancy in epoxy resin

In the present paper, a novel biomass flame retardant based on alginic acid was synthesized through chemical combination with a reactive P–Si compound. Compared with alginates, the modified alginate showed obviously increased thermal stability and water resisting property, as well as better compatibility with epoxy resin, which can satisfy the requirements of a flame‐retardant additive in the polymer. The flame‐retardant properties were evaluated by vertical burning tests, limiting oxygen index, and microscale combustion calorimetry. Due to the self‐charring capacity of alginate combined with the charring catalyst from P and the charring reinforcer from Si, the modified alginate exhibited much better flame retardancy, taking advantage of the formation of a more continuous, denser, and strengthened char layer than either individual alginate or P–Si flame retardant. The corresponding flame‐retardant mechanisms were investigated and discussed. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45552.     

Preparation and properties of novel hybrid resins based on acetylene‐functional benzoxazine and polyvinylsilazane

A serial of addition‐curable hybrid resins for resin matrix of advanced composites are prepared by thermal prepolymerization between acetylene‐functional benzoxazine(BZ) and polyvinylsilazane(PSN) with various weight ratios. Processing capability of BZ‐PSN resin is investigated by measuring viscosity. Cure behavior is investigated by differential scanning calorimetry (DSC) and Fourier transform infrared (FT‐IR) spectra. Thermal property of cured BZ‐PSN resin is investigated by Thermogravimetric analysis (TGA) and Dynamic mechanical analysis (DMA). BZ‐PSN resin shows a low viscosity of 40–180 mPa·s between 60 and 90°C, and maintains the low viscosity for 6 h, indicating that the resin is suitable for resin transfer molding (RTM) process to fabricate composites. DSC results show that BZ‐PSN resin can be cured completely at about 250°C without adding any other curing additives. FT‐IR shows the reaction between BZ and PSN take place. TGA shows that thermal stability of cured BZ‐PSN resin is increased with the content of polyvinylsilazane increasing both in nitrogen and in air. DMA shows cured hybrid resins have excellent thermal properties. The excellent processability and thermal properties suggest that BZ‐PSN resin is a promising candidate for resin matrix of advanced composites. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 3794–3799, 2013     

Effects of the matrix crystallinity,dispersed phase,and processing type on the morphological,thermal, and mechanical properties of polylactide-based binary blends with poly[(butylene adipate)-co-terephthalate] and poly[(butylene succinate)-co-adipate]

In this study, we prepared immiscible blends of 75 wt % polylactide (PLA) with 25 wt % poly[(butylene adipate)-co-terephthalate] (PBAT) through an injection-molding (IM) process and a twin-screw extruder (TSE) followed by IM. An amorphous polylactide (A-PLA) and a semicrystalline polylactide (SC-PLA) were used as the matrixes to investigate the matrix crystallization effect on the morphology and property development of the blends with only IM. A blend of A-PLA with 25 wt % poly[(butylene succinate)-co-adipate] (PBSA) was also prepared through IM to compare its properties with those of the A-PLA–PBAT blends. The morphological, thermal, solid viscoelastic, tensile, and flexural properties of the blends were compared, and their dependency on the evolution of the blend morphology was analyzed. The tensile results show that when IM was used as the sole processing technique, the ductility and toughness were significantly improved only when SC-PLA was used as the matrix. Preprocessing through TSE also resulted in the enhancement of the blend ductility. In A-PLA–PBSA, the vitrification of PLA hindered the crystallization of PBSA to very low temperatures (<0°C) and resulted in a very nonuniform structure with weak intermolecular bonding between phases. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47636.     

Thermophysical properties of bacterial poly(3‐hydroxybutyrate): Characterized by TMA,DSC, and TMDSC

The melting, isothermal and nonisothermal crystallization behaviors of poly(3‐hydroxybutyrate) (PHB) have been studied by means of temperature modulated differential scanning calorimetry (TMDSC) and conventional DSC. Various experimental conditions including isothermal/annealing temperatures (80, 90, 100, 105, 110, 120, 130, and 140°C), cooling rates (2, 5, 10, 20, and 50°C/min) and heating rates (5, 10, 20, 30, 40, and 50°C/min) have been investigated. The lower endothermic peak (T_m1) representing the original crystals prior to DSC scan, while the higher one (T_m2) is attributed to the melting of the crystals formed by recrystallization. Thermomechanical analysis (TMA) was used to evaluate the original melting temperature (T_melt) and glass transition temperature (T_g) as comparison to DSC analysis. The multiple melting phenomenon was ascribed to the melting‐recrystallization‐remelting mechanism of the crystallites with lower thermal stability showing at T_m1. Different models (Avrami, Jeziorny‐modified‐Avrami, Liu and Mo, and Ozawa model) were utilized to describe the crystallization kinetics. It was found that Liu and Mo's analysis and Jeziorny‐modified‐Avrami model were successful to explain the nonisothermal crystallization kinetic of PHB. The activation energies were estimated in both isothermal and nonisothermal crystallization process, which were 102 and 116 kJ/mol in respective condition. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42412.     

Ecofriendly modification of acetosolv lignin from oil palm biomass for improvement of PMMA thermo‐oxidative properties

The environmentally friendly esterification of acetosolv lignin (AL), obtained from pressed oil palm mesocarp fibers, is described, for the improvement of thermo‐oxidative properties of poly(methyl methacrylate) (PMMA) films. Acetylation of AL was performed in ecofriendly conditions using acetic anhydride in the absence of catalysts. Acetylated acetosolv lignin (AAL) was successfully obtained in only 12 min with a solvent‐free and catalyst‐free microwave‐assisted procedure. Lignins were characterized by Fourier transform infrared spectroscopy, size exclusion chromatography, thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC), confirming the efficacy of the methodology employed. AL and AAL as fillers in different concentrations (1% and 5%) were added to PMMA films. The thermal and mechanical properties of the lignin‐incorporated films were analyzed by TGA, DSC, and dynamic mechanical analysis (DMA). The films incorporated with lignin and acetylated lignin presented initial degradation temperature (T_onset) and onset oxidative temperature (OOT) values higher than pure PMMA films, contributing thus to an enhancement of thermo‐oxidative stability of PMMA. The DMA analyses showed that incorporation of AL or AAL increased the storage modulus (E′) of PMMA films, but did not affect their glass‐transition temperatures (T_g). The results indicate the potential use of oil palm mesocarp lignin to enhance the thermo‐oxidative properties of PMMA without compromising its mechanical response. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45498.     

Synthesis of a novel benzoxazine precursor containing phenol hydroxyl groups and its polymer

A novel benzoxazine precursor containing phenol hydroxyl groups was synthesized from bisphenol A, 4,4′‐diaminodiphenyl methane, and formaldehyde with a molar ratio of 2:1:4. The benzoxazine precursor was characterized with Fourier transform infrared, proton nuclear magnetic resonance, and size exclusion chromatography. The curing reaction was monitored by the gel time, differential scanning calorimetry, and Fourier transform infrared. The obtained polybenzoxazine showed high thermal stability and a high glass‐transition temperature. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Super‐tough biodegradable poly(vinyl alcohol)/poly(vinyl pyrrolidone) blends plasticized by glycerol and sorbitol

Tough biodegradable films were prepared using a poly(vinyl alcohol) (PVA)/poly(vinyl pyrrolidone) (PVP) (1:1) blend with plasticizers of glycerol (GLY), sorbitol (SOR), and their (one to one) mixture. We studied the effect of plasticization on the structural, thermal, and mechanical properties of the PVA/PVP blend films. Fourier transform infrared spectra indicated good miscibility of the two components due to the H‐bonding between the PVA and PVP molecules. The addition of plasticizers reduced the interaction between PVA and PVP, evidenced by an increase in the intensity of PVA diffraction peaks observed in the X‐ray diffraction (XRD) characterization. Thermal degradation of the blends increased as a function of the plasticizer used. GLY affected thermal degradation more than SOR and the mixtures. The incorporation of the plasticizers promoted the growth of PVA crystals as evidenced by XRD patterns and the enthalpy of fusion (ΔH_f) obtained by differential scanning calorimetry measurements. The introduction of SOR to the binary blend increased toughness seven times and imparted simultaneous and pronounced improvements to maximum tensile stress and elongation at break. This behavior holds out great promise for the development of a new generation of mechanically robust, yet thoroughly biodegradable materials that could effectively supplant conventional polymers in demanding applications. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46406.     

Biodegradable polyester‐based heat management materials of interest in refrigeration and smart packaging coatings

In this study, two biodegradable matrices, polycaprolactone (PCL) and polylactide (PLA) were used to encapsulate for the first time a phase changing material (PCM), specifically dodecane (a paraffin which has a transition temperature at ?10°C), through the use of the electrospinning technique with the aim of developing coating materials with energy storage capacity for thermal insulation applications. The encapsulation efficiency obtained using both matrices has been studied and the different morphology, thermal properties, and molecular structure of the materials developed were characterized. Results showed that dodecane can be properly encapsulated inside both biopolymers with a submicron drop size, albeit PCL provides better encapsulation performance. A temperature mismatch between melting and crystallization phenomena (the so‐called supercooling effect) was observed in the encapsulated paraffin, mainly ascribed to the reduced PCM drop size inside the fibers. Addition of dodecanol was seen to best act as a nucleating agent for the PCL/PCM and PLA/PCM structures, allowing a significant amount of heat storage capacity for these systems without supercooling. These innovative ultrathin structured biomaterials are of interest as energy storage systems to advantageously coat or wrap temperature sensitive products in refrigeration equipment and constitute smart food or medical/pharmaceutical packaging. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 3251–3262, 2013