Polylactic acid and its blends with petroleum‐based resins: Effects of reprocessing and recycling on properties

Environmental and economic reasons make the use of bioplastics and biocomposites increasingly coveted in sectors other than packaging. Recycling of all wasted or rejected durable plastics is highly desired and biobased plastics are no exception. Therefore, the investigation of pre‐ and post‐consumer recycling of products made from biobased plastics is of great interest. Polylactic acid (PLA) and its blends have been chosen for this study because it is an excellent representative of mass‐produced bioplastics for industrial applications. As part of the “Sustainable Recycling of ‘Green’ Plastics” project, the current study addresses the durability issues related to the reprocessing and post‐consumer recycling of a PLA virgin resin and two commercially available blends of PLA namely one with polycarbonate (PC) and one with polyethylene (PE). The materials were investigated using methods that simulate post‐processing and post‐consumer recycling. Accelerated ageing was performed at elevated temperature and humidity to simulate the usage period of the materials. The materials were analyzed using differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), and their mechanical strength was evaluated by tensile and impact testing. The flow properties of the materials were characterized by the melt flow index (MFI). Multiple processing of pure PLA did not affect the impact strength or the glass transition temperature (T_g), but caused crystallization and increase in the MFI, indicating that degradation occurred during processing. DSC thermograms of the blends revealed that the components in the blends were not miscible. Multiple processing of the blends did not significantly affect the elastic modulus of the materials, but affected the elongation at break. The results indicated that multiple processing of the PLA/HDPE blend caused increased dispersion and thus increased elongation at break, while the dominating mechanism in the PLA/PC blend was degradation that caused a decrease in elongation at break. Post‐consumer recycling of the PLA/PC blend was simulated and the results clearly showed that ageing corresponding to one year of use caused a significant degradation of PLA. Pure PLA was severely degraded after only one ageing cycle. Although the PLA/PC blend showed some improved mechanical properties and resistance to degradation compared with pure PLA, one ageing cycle still caused a severe degradation of the PLA and even the PC was degraded as indicated by the formation of small amounts of bisphenol A. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43916.     

Bio‐inspired “green” nanocomposite using hydroxyapatite synthesized from eggshell waste and soy protein

Eco‐friendly and inexpensive “ green” nanocomposites with enhanced functional performances were developed by combining nanoscale hydroxyapatite (HA) synthesized from eggshell waste (nEHA) and protein‐based polymer extracted from defatted soybean residues. nEHA was synthesized from chicken eggshells using an energy efficient microwave‐assisted wet chemical precipitation method. Transmission electron microscopy, X‐ray diffraction, and energy‐dispersive X‐ray spectroscopy studies confirmed the nanometer scale (diameter: 4–14 nm and length: 5–100 nm) of calcium‐deficient (Ca/P ratio ～1.53) needle‐like HA. Uniform dispersion of nEHA in soy protein isolate (SPI) solution was obtained by modifying nEHA surface using a polyelectrolyte (sodium polyacrylate) dispersant via irreversible adsorption. Green nanocomposite films were prepared from SPI and surface‐modified nEHA with the help of a natural plasticizer “glycerol” by solution casting. Significant improvements in tensile modulus and strength were achieved owing to the inclusion of uniformly dispersed nEHA in SPI sheets. Overall, this work provides a green pathway of fabricating nanocomposites using naturally occurring renewable polymer and inorganic moieties from eggshell waste that emphasizes the possibilities for replacing some petroleum‐based polymers in packaging and other applications. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43477.     

Study on the preparation and mechanical properties of injection‐moulded wood‐based plastics

The objectives of this study were to prepare injection‐moulded wood‐based plastics and to characterize their mechanical properties. Injection‐moulded wood‐based plastics with satisfactory flexural (65.7 MPa) and tensile strengths (30.1 MPa) were successfully obtained through a simple reaction of mulberry branch meal with phthalic anhydride (PA) in 1‐methylimidazole under mild condition. The X‐ ray diffraction results indicated complete disruption of the crystallinity of cellulose because the pattern obtained for esterified fiber was almost a straight line without any peaks. The peaks in the Fourier transform infrared spectroscopy spectra (1738 and 748 cm^?1) and NMR spectra (173.3 and 133.5 ppm) indicated the attachment of 0‐carboxybenzoyl groups onto the wood fibers via ester bonds. The differential scanning calorimetry curves showed that the glass transition temperature decreased with increasing weight percentage gain (WPG). The derivative thermogravimetric analysis curves indicated that esterified wood fiber was less thermally stable than the untreated fiber and that the component tends to be homogeneous with increasing WPG. Scanning electron microscope revealed that the fractured surfaces of most samples were smooth and uniform but that high temperature and less PA dosage could lead to the appearance of holes and cracks. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41376.     

Keratin–polyhydroxyalkanoate melt‐compounded composites with improved barrier properties of interest in food packaging applications

Sustainable biocomposite materials based on the combination of polyhydroxyalkanoates with a keratin additive derived from poultry feathers were successfully developed via melt compounding. Suitable dispersions for low loadings of the additive in the biopolymeric matrix were achieved by the melt‐mixing technique. A good physical interaction between the polymeric matrix and the additive was observed by scanning electron microscopy (SEM). Reductions in water, limonene, and oxygen permeability of the pure polymer to less than a half of its initial value for the composite containing 1 wt % of keratin additive were achieved. This composition was also found to exhibit optimum mechanical performance. As a result, these materials offer significant potential in fully renewable packaging applications based on polyhydroxyalkanoates with enhanced barrier performance. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39947.     

Improvement of the thermal properties of poly(3‐hydroxybutyrate) (PHB) by low molecular weight polypropylene glycol (LMWPPG) addition

In this work, blends of poly(3‐hydroxybutyrate) (PHB) with 5, 10, 15, and 20 wt % low molecular weight poly(propylene glycol) (LMWPPG) have been prepared and characterized by scanning electron microscopy (SEM), Fourier transform infrared (FTIR) with attenuated total reflectance (ATR) accessory and simultaneous thermal analysis (TG/DTA). FTIR and thermal analyses suggested that the presence of LMWPPG led to a maximum crystallinity for the blend PHB/PPG (90/10) blend. The presence of LMWPPG also caused a significant increase of the PHB processability window, i.e., the difference of the melting and degradation temperature, of PHB from 105 to 134°C, which is extremely important for the industrial uses of PHB. This PHB stabilization effect is discussed in terms of an intermolecular interaction of the PHB carbonyl with LMWPPG methyl groups which probably hinders the classical radon β‐scission PHB intramolecular decomposition mechanism. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Fully bio‐based polyesters derived from 2,5‐furandicarboxylic acid (2,5‐FDCA) and dodecanedioic acid (DDCA): From semicrystalline thermoplastic to amorphous elastomer

A serials of fully bio‐based poly(ethylene dodecanedioate‐2,5‐furandicarboxylate) (PEDF) were synthesized from Dodecanedioic acid (DDCA), 2,5‐Furandicarboxylic acid (2,5‐FDCA), and ethylene glycol through a two‐step procedure consisted of transesterification and polycondensation. After their chemical structures were confirmed by Nuclear Magnetic Resonance and Fourier Transform Infrared Spectroscopy, their thermal, mechanical, and biodegradation properties were investigated in detail. Results showed that the chemical composition of PEDFs could be easily controlled by the feeding mole ratio of DDCA to FDCA and they possessed the characteristic of random copolyester with the intrinsic viscosity ranged from 0.82 to 1.2 dL/g. With the varied mole ratio of DDCA to FDCA, PEDFs could be changed from semicrystalline thermoplastic to the completely amorphous elastomer, indicated by the elongation at break ranged from 4 for poly(ethylene 2,5‐furandicarboxylate) to 1500% for amorphous PEDF‐40. The amorphous PEDF‐30 and PEDF‐40 showed satisfactory shape recovery after cyclic tensile test, which was the typical behavior for elastomer. Enzymatic degradation test indicated that all the PEDFs were biodegradable and the degradation rate was heavily affected by their chemical compositions. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46076.     

Thermoplastic elastomers derived from bio‐based monomers

Series of copolyesters based on poly(propylene succinate) (PPS) and poly(butylene succinate) (PBS), which can be produced from biological feedstock, and postconsumer poly(ethylene terephthalate) (PET) were synthesized with the aim of developing sustainable materials, which combine the mechanical properties of high performance elastomers with those of flexible plastics. The aliphatic polyesters were synthesized by the catalyzed two‐step transesterification reaction of dimethyl succinate, 1,3‐propanediol, and 1,4‐butanediol followed by melt reaction with PET in bulk. The content of PET segments in the polymer chains was varied from about 10 to 100 wt % per 100 wt % PPS or PBS. The effect of the introduction of the PET segments on the structure, thermal, physical, and mechanical properties was investigated. The composition and structure of these aliphatic/aromatic copolyesters were determined by NMR spectroscopy. The thermal properties were investigated using differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The level of crystallinity was studied by means of DSC and wide‐angle X‐ray scattering. A depression of melting temperature and a reduction of crystallinity of copolyesters with increasing content of PET segments were observed. Consequently, the tensile modulus and strength of copolyesters decreased, and the elongation at break increased with PET content in the range of 10?50 wt %. Thus, depending on PET content, the properties of copolyesters can be tuned ranging from semicrystalline polymers possessing good tensile modulus (380 MPa) and strength (24 MPa) to nearly amorphous polymer of high elongation (～800%), and therefore they may find applications in thermoplastics as well as elastomers or impact modifiers. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39815.     

Effect of freeze‐thaw pretreatment on thermal drying process and physicochemical properties of chitosan

The effect of freeze‐thaw pretreatment on the thermal drying process and physicochemical properties of chitosan was investigated in this study. Results showed that the freeze‐thaw treatment changed the form of chitosan paste and reduced 75.6–77.7% of the water content. The freeze‐thaw treatment decreased the drying time of chitosan from 16–19 h to 2.75–4 h and the dried product was loosely packed powder. After freeze‐thaw treatment, the molecular weight of chitosan was unchanged during the thermal drying. The heat‐induced browning effect of chitosan during drying was greatly alleviated by the pretreatment. Furthermore, the pretreatment increased the 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH) radical‐scavenging activity of dried product by 40.4–59.8%. The molecular weight, color, and DPPH radical‐scavenging activity of the pretreated dried chitosan product were close to those of freeze‐dried product. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41017.     

Potato protein isolate‐based biopolymers

Thermal processing of two potato protein isolates (PPIs) with glycerol as a plasticizer was explored in this study. The PPIs were pretreated by alkali or alkali under reducing conditions. The PPIs before and after pretreatment were analyzed by sodium dodecyl sulfate polyacrylamide gel electrophoresis, differential scanning calorimetry, and Fourier transform infrared spectroscopy. The effects of plasticizer content and pretreatment on mechanical and thermo‐mechanical properties of the compression‐molded biopolymers were studied. The highest tensile strengths obtained were 20–25 MPa and the biopolymer can be brittle or ductile depending on the plasticizer contents. The molecular weight and protein structure of the PPIs markedly affected the resultant biopolymers’ static and dynamic mechanical properties. The pretreatment of PPIs caused distinctly different changes in the mechanical properties of the two PPIs. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42723.     

Synthesis,characterization, and properties of acrylate‐modified tung‐oil waterborne insulation varnish

An acrylate‐modified tung‐oil waterborne insulation varnish was synthesized from tung oil, maleic anhydride, and acrylates via a Diels–Alder reaction and free‐radical polymerization, and the varnish could be solidified at a relatively low temperature with blocked hexamethylene diisocyanate as a curing agent. The resulting films were characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, and differential scanning calorimetry. The insulation properties (electrical insulation strength, volume resistivity, and surface resistivity) of the varnish films were tested, and the resistances of films to salted water were evaluated. With an increase in the maleic anhydride content, the thermal stability of the film was improved, whereas the electrical insulation strength, volume resistivity, and surface resistivity decreased. The electrical insulation strength of the film after it was immersed in the NaCl solution was lower than that in dry state, and it decreased as the immersed time was prolonged. In particular, the electrical insulation strength loss of the film increased significantly at maleic anhydride contents beyond 25 wt %. Furthermore, the hardness of the film increased with increasing methyl methacrylate/N‐butyl acrylate ratio, whereas the flexibility and adhesion of film decreased to a certain degree at the same time. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41608.     

Development and characterization of green composites from bio‐based polyethylene and peanut shell

In the present work, different compatibilizers, namely polyethylene‐graft‐maleic anhydride (PE‐g‐MA), polypropylene‐graft‐maleic anhydride (PP‐g‐MA), and polystyrene‐block‐poly(ethylene‐ran‐butylene)‐block‐polystyrene‐graft‐maleic anhydride (SEBS‐g‐MA) were used on green composites derived from biobased polyethylene and peanut shell (PNS) flour to improve particle–polymer interaction. Composites of high‐density polyethylene/peanut shell powder (HDPE/PNS) with 10 wt % PNS flour were compatibilized with 3 wt % of the abovementioned compatibilizers. As per the results, PP‐g‐MA copolymer lead to best optimized properties as evidenced by mechanical characterization. In addition, best particle–matrix interface interactions with PP‐g‐MA were observed by scanning electron microscopy (SEM). Subsequently HDPE/PNS composites with varying PNS flour content in the 5–30 wt % range with PP‐g‐MA compatibilizer were obtained by melt extrusion and compounding followed by injection molding and were characterized by mechanical, thermal, and morphological techniques. The results showed that PNS powder, leads to an increase in mechanical resistant properties (mainly, flexural modulus, and strength) while a decrease in mechanical ductile properties, that is, elongation at break and impact absorbed energy is observed with increasing PNS flour content. Furthermore, PNS flour provides an increase in thermal stability due to the natural antioxidant properties of PNS. In particular, composites containing 30 wt % PNS powder present a flexural strength 24% and a flexural modulus 72% higher than the unfilled polyethylene and the thermo‐oxidative onset degradation temperature is increased from 232 °C up to 254 °C thus indicating a marked thermal stabilization effect. Resultant composites can show a great deal of potential as base materials for wood plastic composites. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43940.     

Evaluation of 1‐ethyl‐3‐methylimidazolium acetate based ionic liquid systems as a suitable solvent for collagen

Collagen, a prominent biopolymer, which is famous for its excellent biological activity, has been used extensively for tissue engineering applications. In this study, a novel solvent system for collagen was developed with an ionic liquid, 1‐ethyl‐3‐methylimidazolium acetate ([EMIM][Ac]), solvent system. A series of sodium salts were introduced into this solvent system to enhance collagen's dissolution procedure. The results show that the solubility of collagen was significantly influenced by the temperature and sodium salts. The solubility reached up to approximately 11% in the [EMIM][Ac]/Na₂HPO₄ system at 45°C. However, the structure of the regenerated collagen (Col‐regenerated) may have been damaged. Hence, we focused on the structural integrity of the collagen regenerated from the [EMIM][Ac] solvent system by the methods of sodium dodecyl sulfate–polyacrylamide gel electrophoresis, Fourier transform infrared spectroscopy, ultrasensitive differential scanning calorimetry, atomic force microscopy, X‐ray diffraction, and circular dichroism because its signature biological and physicochemical properties were based on its structural integrity. Meanwhile, a possible dissolution mechanism was proposed. The results show that the triple‐helical structure of collagen regenerated from the [EMIM][Ac] solvent system below 35°C was retained to a large extent. The biocompatibility of Col‐regenerated was first characterized with a fibroblast adhesion and proliferation model. It showed that the Col‐regenerated had almost the same good biological activity as nature collagen, and this indicated the potential application of [EMIM][Ac] in tissue engineering. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 2245–2256, 2013     

Synthesis and properties of cross‐linked polymers from epoxidized rubber seed oil and triethylenetetramine

A series of epoxidized oils were prepared from rubber seed, soybean, jatropha, palm, and coconut oils. The epoxy content varied from 0.03 to 7.4 wt %, in accordance with the degree of unsaturation of the oils (lowest for coconut, highest for rubber seed oil). Bulk polymerization/curing of the epoxidized oils with triethylenetetramine (in the absence of a catalyst) was carried out in a batch setup (1 : 1 molar ratio of epoxide to primary amine groups, 100°C, 100 rpm, 30 min) followed by casting of the mixture in a steel mold (180°C, 200 bar, 21 h) and this resulted in cross‐linked resins. The effect of relevant pressing conditions such as time, temperature, pressure, and molar ratio of the epoxide and primary amine groups was investigated and modeled using multivariable nonlinear regression. Good agreement between experimental data and model were obtained. The rubber seed oil‐derived polymer has a T_g of 11.1°C, a tensile strength of 1.72 MPa, and strain at break of 182%. These values are slightly higher than for commercial epoxidized soybean oil (T_g of 6.9°C, tensile strength of 1.11 MPa, and strain at break of 145.7%). However, the comparison highlights the potential for these novel resins to be used at industrial/commercial level. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42591.     

Effect of two different plasticizers on the properties of poly(3‐hydroxybutyrate) binary and ternary blends

Plasticized poly(3‐hydroxybutyrate) (PHB) films were obtained by solvent casting. The effects of two different additives on several properties of PHB have been examined, utilizing tributyrin and poly[di(ethyleneglycol) adipate] (A). Based on changes in the glass transition temperature (T_g) and cold crystallization temperature of host PHB, the two components are miscible with PHB and they can act as plasticizers. Binary and ternary blends were obtained by adding both plasticizers separately or together, respectively. The effect of plasticizer addition on the optical transparency, water vapor permeability, and tensile properties of the films was studied. It was found that the blends remain transparent and water vapor permeability was maintained constant until a 20 wt % of plasticizer content. Plasticizing effect was corroborated and it depended on the plasticizer percentage. Binary blends had an increased plasticity, in concordance with T_g diminution of PHB. Although ternary blends presented T_g diminution, mechanical properties were not improved probaby due to strong interactions between plasticizers. Finally, binary and ternary blends presented enhanced properties, causing an increment on processability. A correct knowledge between the formulation of the film and the role played by each component could allow getting custom films. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46016.     

Antibacterial polymer composites based on low‐density polyethylene and essential oils immobilized on various solid carriers

In this study, we investigated the antibacterial modification of polymers with biologically active substances in essential oils [EOs; linalool, 4‐allylanisole (ALY), and trans‐anethole]. These compounds were thermoplastically incorporated into a low‐density polyethylene matrix via solid inert carriers [wood flour (WF) and talc and molecular sieves] with physically immobilized EOs. The concentrations of the antibacterial modifiers on the carriers and in the resulting composites were determined with three chromatographic techniques (gas chromatography with mass spectrometry, pyrolysis and gas chromatography with mass spectrometry, and high‐performance liquid chromatography). The effects of such modifications to the mechanical properties of the prepared composites were studied by stress–strain analysis. Interactions on the polymer matrix carriers were observed by scanning electron microscopy. The prepared composites were also tested for antibacterial activity against both Gram‐negative and Gram‐positive bacterial strains. The highest efficiency of isothermal immobilization was found for systems consisting of ALY and WF. This finding was in accordance with microbiological studies. The phase of immobilizing the EOs did not influence the mechanical properties of the studied composites. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42816.     

Polypropylene composites obtained from self‐reinforced hybrid fiber system

The purpose of the study was to obtain a composite material with the self‐reinforced structure, which processing provide increased mechanical properties. The composites used in presented work were prepared from the two types of fiber mixtures, both were based on polypropylene fibers, the difference was in used cellulose or wood flour filler. Composites were prepared using the hot compaction method. The presented research describes the effect of the composite composition and processing conditions. The results include the static tension measurements, tensile impact tests and thermal analysis, including: DSC and DMTA. The structure has been studies using the SEM observations. Results of presented studies confirm the self‐reinforcing effect in obtained hybrid composites. It provides in the comparison to the standard wood polymer composites to the higher level of material reinforcement with lower amount of natural filler. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43283.     

Antioxidant and physicochemical properties of blended films based on gelatin‐sodium caseinate activated with natural extracts

Blend films of pigskin gelatin (GEL) and sodium caseinate (SCas) with boldo (B), guarana (G), cinnamon (C), or rosemary (R) extracts added were studied. SCas and extracts addition in blend films significantly increased the gloss and better UV barrier of GEL100 films. Extracts incorporation significantly decreased the rigidity and elongation of GEL100 films, which were significantly improved in GEL75:SCas25 blend films with extracts (EM = 295.69 ± 21.75 MPa and EB = 11.60 ± 3.43%). SCas addition not affected the TS parameter. The water vapor permeability of GEL100 films was reduced in blended films with extracts, showing the lowest value for GEL75:SCas25 + R (0.99 ± 0.07 × 10¹⁰ g s^?1 m^?1 Pa^?1). FTIR and microstructure analyses showed good compatibility for all components. The antioxidant activity of GEL100 was significantly increased with SCas and extracts addition (GEL50:SCas50 + R = 4.31 ± 0.11 mM ), suggesting the application of these films as an active food packaging material. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44467.     

Approach in Macadamia integrifolia residue based low-density polyethylene composites on mechanical and thermal performance

Macadamia nutshell residues are generated in large quantities, around 70%–77% for each ton produced, and it is a waste material with high techno-economic potential. This work purpose a sustainable alternative to valorize macadamia nutshell residues (MN) as reinforcing in low-density polyethylene (LDPE) composites through melt mixing, using different fiber contents (0, 5, 10, and 20 wt%), and investigate the influence of fibers (residues) in composites by mechanical tests and thermal analysis. The fibers addition has significantly increased the composites' stiffness compared with neat LDPE, causing a reduction of toughness and resilience, leading to lower impact energy absorption. The LPDE/MN20% composite obtained the best tensile and flexural mechanical performance, resulting in a maximum modulus, which implies an increase of 36.9% and 77.6% compared with the neat LDPE. The addition of macadamia fibers on the composites acted as nucleation points of spherulites, which promoted an increase in the crystallization degree. Consequently, better performance of mechanical properties was observed in the green composites. Thus, the macadamia nutshell residues present a promising future as filler in LDPE for enhancing composites' thermal and mechanical properties.     

Characterization of polyhydroxybutyrate biosynthesized from crude glycerol waste using mixed microbial consortia

This study focused on the characterization of polyhydroxybutyrate (PHB) produced from crude glycerol (CG) using mixed microbial consortia (MMC). PHB recovered from two biomass drying treatments (65°C oven drying and lyophilization) was characterized comparatively along with a commercially sourced PHB (PHB‐C). Characterization results showed that oven‐drying method caused PHB partial hydrolysis, as indicated by its lower molecular weight (M_w) (PHB‐O, 144,000 g mol^?1), which further affected its physical and chemical properties. Lyophilization helped alleviate PHB hydrolysis during drying process, leading to PHB (PHB‐L) of higher M_w (309,000 g mol^?1) and material properties comparable with commercial PHB. Furthermore, crystallization and morphological studies showed that PHB‐L featured faster crystallization rates and smaller spherulites as compared with PHB‐C, probably due to its lower M_w. In general, the results from this study suggested that CG‐MMC‐derived PHB‐L possessed material properties comparable with those of pure substrate/culture produced PHB. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Polyurethane coatings from liquefied wood containing remains of a copper‐, chromium‐, and boron‐based wood preservative

Preparation of polyurethane wood coatings based on copper‐, chromium‐, and boron (CCB) containing liquefied wood was performed, as an alternative way to manage postconsumed preservative‐contaminated wood. Additionally, we examined the possibility of improvement of selected properties of the liquefied wood‐based coatings by an addition of silica nanoparticles. The constituents of the CCB wood preservative do not exhibit an influence on a liquefaction process and on composition of the liquefied mixture. CCB also does not affect curing of the formulations containing liquefied wood and an isocyanate‐type hardener. Furthermore, influence of CCB on adhesion strength of liquefied wood‐based coatings on a wooden substrate, their hardness, and resistance to scratching and to water, acetone, and alcohol, is not exhibited. However, apart from these, from the applicative point of view, positive results, any improvement of the coating properties by the addition of silica nanoparticles is not shown. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40865.