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Abstract Hydrogels present attractive opportunities as flexible sensors due to their soft nature and tunable physicochemical properties. Despite significant advances, practical application of hydrogel‐based sensor is limited by the lack of general routes to fabricate materials with combination of mechanical, conductive, and biological properties. Here, a multi‐functional hydrogel sensor is reported by in situ polymerizing of acrylamide (AM) with N,N′‐bis(acryloyl)cystamine (BA) dynamic crosslinked silver‐modified polydopamine (PDA) nanoparticles, namely PAM/BA‐Ag@PDA. Compared with traditional polyacrylamide (PAM) hydrogel, the BA‐Ag@PDA nanoparticles provide both high‐functionality crosslinks and multiple interactions within PAM networks, thereby endowing the optimized PAM/BA‐Ag@PDA hydrogel with significantly enhanced tensile/compressive strength (349.80 kPa at 383.57% tensile strain, 263.08 kPa at 90% compressive strain), lower hysteresis (5.2%), improved conductivity (2.51 S m−1) and excellent near‐infrared (NIR) light‐triggered self‐healing ability. As a strain sensor, the PAM/BA‐Ag@PDA hydrogel shows a good sensitivity (gauge factor of 1.86), rapid response time (138 ms), and high stability. Owing to abundant reactive groups in PDA, the PAM/BA‐Ag@PDA hydrogel exhibits inherent tissue adhesiveness and antioxidant, along with a synergistic antibacterial effect by PDA and Ag. Toward practical applications, the PAM/BA‐Ag@PDA hydrogel can conformally adhere to skin and monitor subtle activities and large‐scale movements with excellent reliability, demonstrating its promising applications as wearable sensors for healthcare.

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Citric acid-epoxidized soybean oil oligomers (CESO) were prepared and utilized to improve the properties of corn starch-based bioplastics. CESO were synthesized by controlling the stoichiometric ratio of acid equivalent weight and epoxy equivalent weight at 3:1. Starch-based bioplastics with satisfactory properties were fabricated through solution casting. Analysis including FTIR, molecular distribution, and polydispersity index validated the ring opening polymerization of ESO and CA. The hydrogen bond and crosslinking interactions between CESO and starch were evidenced by the FTIR. SEM micrographs suggested that CESO exhibited better compatibility with starch than ESO. X-ray diffraction patterns of the bioplastics were changed apparently by CESO due to the crosslinking interaction. Swelling degree and opacity of the bioplastics reduced significantly after the introduction of CESO, while tensile strength increased remarkably from 5.62 to 6.93 MPa (p

An environmentally friendly Pickering stabilizer was developed by upcycling sugarcane bagasse (SCB) into a cellulose nanocrystal (CNC), which was subjected to surface modification by using quaternary ammonium compound to enhance its amphiphilic characteristics. The changes in microstructural properties of modified cellulose nanocrystal (m-CNC), such as surface functional group, thermal stability, surface morphology, elemental composition, and particle size distribution were investigated. Results indicated the success of quaternary ammonium compound grafting with the presence of a trimethyl-alkyl chain on the cellulose structure, while the m-CNC preserves the needle-like nanoparticles in length of ~534 nm and width of ~20 nm. The colloidal profile of m-CNC-stabilized oil–water emulsion gels with different concentrations of m-CNC (1–5 wt%), and oil:water (O:W) ratios (3:7, 5:5, 7:3) were examined. The emulsion gel stability study indicated that the optimal concentration of m-CNC (3 wt%) was able to stabilize all the emulsion gels at different O:W ratios with an emulsion index of >80% for 3 months. It is the minimum concentration of m-CNC to form a robust colloidal network around the small oil droplets, leading to the formation of stable emulsion gels. The emulsion gel with O:W ratio (3:7) with 3 wt% of m-CNC rendered the best m-CNC–oil-droplets dispersion. The m-CNC effectively retained the size of oil droplets (

The installation of a corona ring on an insulator string on a transmission line is one of the solutions to reduce the electric field stress surrounding the energised end of the insulator string. However, installing a corona ring with an optimum design to reduce the electric field magnitude on an insulator string is a challenging task. Therefore, in this work, a method to achieve the optimum design of a corona ring for 132 kV composite non-ceramic insulator string was proposed using two optimisation methods: the Imperialist Competitive Algorithm (ICA) and Grey Wolf Optimisation (GWO). A composite non-ceramic insulator string geometry with and without a corona ring was modelled in finite element analysis and used to obtain the electric field distribution in the model geometry. The electric field distribution was evaluated using a variation in the corona ring’s dimensions, i.e., the ring diameter, the ring tube diameter and the vertical position of the ring along the insulator string. From the results achieved, a comparison of the minimum electric field magnitude along the insulator string with a corona ring design shows that the minimum electric field magnitude is found to be lower using optimisation techniques compared to without using optimisation techniques by between 3.724% and 3.827%. Hence, this indicates the capability and effectiveness of the proposed methods in achieving the optimum design of a corona ring on an insulator string.

Exploiting plant extracts to form metallic nanoparticles has been becoming the promising alternative routes of chemical and physical methods owing to environmentally friendly and abundantly renewable resources. In this study, Momordica charantia and Psidium guajava leaf extract (MC.broth and PG.broth) are exploited to fabricate two kinds of biogenic silver nanoparticles (MC.AgNPs and PG.AgNPs). Phytoconstituent screening is performed to identify the categories of natural compounds in MC.broth and PG.broth. Both extracts contain wealthy polyphenols which play a role of reducing agent to turn silver (I) ions into silver nuclei. Trace alkaloids, rich saponins and other oxygen-containing compounds creating the organic corona surrounding nanoparticles act as stabilizing agents. MC.AgNPs and PG.AgNPs are characterized by UV-vis and FTIR spectrophotometry, EDS and TEM techniques. FTIR spectra indicate the presence of O-H, C = O, C-O-C and C = C groups on the surface of silver nanoparticles which is corresponded with three elements of C, O and Ag found in EDS analysis. TEM micrographs show the spherical morphology of MC.AgNPs and PG.AgNPs. MC.AgNPs were 17.0 nm distributed in narrow range of 5-29 nm, while the average size of PG.AgNPs were 25.7 nm in the range of 5-53 nm. Further, MC.AgNPs and PG.AgNPs exhibit their effectively inhibitory ability against A. niger, A. flavus and F. oxysporum as dose-dependence. Altogether, MC.AgNPs and PG.AgNPs will have much potential in scaled up production and become the promising fungicides for agricultural applications.

This study examined the development of starch/oil palm empty fruit bunch-based bioplastic composites reinforced with either epoxidized palm oil (EPO) or epoxidized soybean oil (ESO), at various concentrations, in order to improve the mechanical and water-resistance properties of the bio-composites. The SEM micrographs showed that low content (0.75 wt%) of epoxidized oils (EOs), especially ESO, improved the compatibility of the composites, while high content (3 wt%) of EO induced many voids. The melting temperature of the composites was increased by the incorporation of both EOs. Thermal stability of the bioplastics was increased by the introduction of ESO. Low contents of EO led to a huge enhancement of tensile strength, while higher contents of EO showed a negative effect, due to the phase separation. The tensile strength increased from 0.83 MPa of the control sample to 3.92 and 5.42 MPa for the composites with 1.5 wt% EPO and 0.75 wt% ESO, respectively. EOs reduced the composites’ water uptake and solubility but increased the water vapor permeability. Overall, the reinforcing effect of ESO was better than EPO. These results suggested that both EOs can be utilized as modifiers to prepare starch/empty-fruit-bunch-based bioplastic composites with enhanced properties.

Palm kernel shell (PKS) core fibers, an agricultural waste, were chemically modified using N-(3-chloro-2-hydroxypropyl) trimethylammonium chloride (CHMAC) as a quaternizing agent. The potential of quaternized palm kernel shell (QPKS) as an adsorbent for fluoride in an aqueous solution was then studied. The quaternized palm kernel shell (QPKS) core fibers were characterized using Fourier transform infrared spectroscopy (FTIR) and a scanning electron microscope (SEM). The effect of various factors on the fluoride sequestration was also investigated. The results showed that with an increase in the adsorbent amount and contact time, the efficiency of fluoride removal was improved. The maximum fluoride uptake was obtained at pH 3 and a contact time of 4 h. The adsorption behavior was further investigated using equilibrium isotherms and kinetics studies. The results from these studies fit well into Freundlich, Redlich-Peterson, and Sips isotherm’s with a coefficient of determination (R2) of 0.9716. The maximum fluoride removal was 63%. For kinetics studies, the pseudo-second order was the best fit for fluoride, with an R2 of 0.999. These results suggest that QPKS has the potential to serve as a low-cost adsorbent for fluoride removal from aqueous solutions.

The properties of poly(lactic acid) (PLA) bio-composite films reinforced with oil palm empty fruit bunch (OPEFB) fiber and nanosilica were studied in this work. The composite films were prepared via the solvent casting method. The composites were characterized via Fourier transform infrared spectroscopy (FTIR), UV-visible spectroscopy, field-emission scanning electron microscopy (FESEM), tensile testing, and X-ray diffraction (XRD). Ultraviolet visible spectroscopy results revealed that the PLA-based composites and neat PLA had similar light transmittances of approximately 89%. The FTIR and FESEM results showed that OPEFB fibers and nanosilica were embedded into the PLA matrix. The tensile strength of the composites with addition of nanosilica increased with an increasing fiber load content. The XRD analysis showed that the addition of organic or inorganic silica reduced the crystallinity of the composites. The water vapor permeability test results indicated that the inorganic silica decreased the diffusion rate of water molecules through the polymer film. The OPEFB-reinforced PLA blend with additional organic silica exhibited a higher thermal stability than the composites reinforced with inorganic silica.

Low density polyethylene (LDPE), carbon black (CB), and oil palm empty fruit bunch (OPEFB) fiber composites were prepared by melt blending and compression molded into sheets. The effects of incorporated fibers on the electrical conductivity, thermal conductivity, tensile properties, and thermal degradation of the composites were investigated. FTIR results suggest that the OPEFB fibers interact poorly with the polymer matrix and lead to a decrease in mechanical properties. The electrical conductivity of the composites decreased with increasing OPEFB fiber content. Despite the slight decline in conductivity, the composites still were sufficiently conductive relative to applications such as sensors and electromagnetic shielding after the fiber addition. Reduction in thermal conductivity by as much as 10.9% was observed with the addition of 20% OPEFB fiber into LDPE/CB composites. The thermal stability of LDPE/CB/OPEFB fiber composites decreased with increasing fiber content because of the low thermal stability of the incorporated natural fiber.

This study describes an inexpensive, simple and green method to form silver nanoparticles from different leaf extracts of Achyranthes aspera and Scoparia dulcis plants. The silver nitrate is reduced by Achyranthes aspera and Scoparia dulcis leaf extracts respectively to generate two silver nanoparticle types symbolized as AA.AgNPs and SD.AgNPs. The optical absorption, size and morphology of silver nanoparticles are significantly impacted by extract types. The ultraviolet visible spectrum of AA.AgNPs shows a 433-nm peak being more broadened than that of SD.AgNPs. The Fourier infrared transform spectra of two of these silver nanoparticles revealed that their surface is modified by organic constituents from extracts, and thus they are stabilized in solution without any additional reaction. Images from transmission electron microscopy and scanning electron microscope indicate that AA.AgNPs are in clusters with the size of 8–52 nm almost possessing oval shape, while SD.AgNPs are smaller size of 5-45 nm separated well in diversified shapes (spherical, triangle, quadrilateral and hexagonal). Moreover, both AA.AgNPs and SD.AgNPs exhibit the highly antifungal effect against Aspergillus niger, Aspergillus flavus and the most strong impact on Fusarium oxysporum. For these obtained results, two new silver nanoparticles are promising fungicides for various applications of medical and agricultural fields.

Phytoconstituents presenting in herbal plant broths are the biocompatible, regenerative, and cost-effective sources that can be utilized for green synthesis of silver nanoparticles. Different plant extracts can form nanoparticles with specific sizes, shapes, and properties. In the study, we prepared silver nanoparticles (P.uri.AgNPs, P.zey.AgNPs, and S.dul.AgNPs) based on three kinds of leaf extracts (Phyllanthus urinaria, Pouzolzia zeylanica, and Scoparia dulcis, respectively) and demonstrated the antifungal capacity. The silver nanoparticles were simply formed by adding silver nitrate to leaf extracts without using any reducing agents or stabilizers. Formation and physicochemical properties of these silver nanoparticles were characterized by UV-vis, Fourier transforms infrared spectroscopy, scanning electron microscope, transmission electron microscope, and energy dispersive X-ray spectroscopy. P.uri.AgNPs were 28.3 nm and spherical. P.zey.AgNPs were 26.7 nm with hexagon or triangle morphologies. Spherical S.dul.AgNPs were formed and they were relatively smaller than others. P.uri.AgNPs, P.zey.AgNPs and S.dul.AgNPs exhibited the antifungal ability effective against Aspergillus niger, Aspergillus flavus, and Fusarium oxysporum, demonstrating their potentials as fungicides in the biomedical and agricultural applications.

Natural fibers are fine examples of renewable resources that play an important role in the composites industry, which produces superior strength comparable to synthetic fibers. Poly(vinyl alcohol) (PVA) composites in particular have attracted enormous interest in view of their satisfactory performance, properties and biodegradability. Their performance in many applications such as consumer, biomedical, and agriculture is well defined and promising. This paper reviews the utilization of natural fibers from macro to nanoscale as reinforcement in PVA composites. An overview on the properties, processing methods, biodegradability, and applications of these composites is presented. The advantages arising from chemical and physical modifications of fibers or composites are discussed in terms of improved properties and performance. In addition, proper arrangement of nanocellulose in composites helps to prevent agglomeration and results in a better dispersion. The limitations and challenges of the composites and future works of these bio-composites are also discussed. This review concludes that PVA composites have potential for use in numerous applications. However, issues on technological feasibility, environmental effectiveness, and economic affordability should be considered.

Flexible poly(vinyl chloride) (PVC) was fabricated using a palm oil-based alkyd as a co-plasticizer to di-octyl phthalate (DOP) and di-isononyl phthalate (DiNP). The effects of the incorporation of the palm oil-based alkyd on morphological, thermal and mechanical properties of PVC compounds were studied. Results showed the incorporation of the alkyd enhanced the mechanical and thermal properties of the PVC compounds. Fourier transform infrared spectroscopy (FTIR) results showed that the polar –OH and –C=O groups of alkyd have good interaction with the –C–Cl group in PVC via polar interaction. The morphological results showed good incorporation of the plasticizers with PVC. Improved tensile strength, elastic modulus, and elongation at break were observed with increasing amount of the alkyd, presumably due to chain entanglement of the alkyd with the PVC molecules. Thermogravimetric analysis results confirmed that the alkyd has improved the thermostability of the PVC compounds.

A photocatalytic fiber was prepared by modifying the surface of jute fiber with a Bi2O3/TiO2 composite. Maleic acid was used as an organic linker, and the coating process was conducted with heat-treatment at 240 °C. At first, the Bi2O3/TiO2 composite was synthesized by incorporating TiO2 nanoparticles onto a Bi2O3 phase. Subsequently, the photocatalytic fiber was prepared by incorporating the Bi2O3/TiO2 composite onto the surface of the fiber. The Bi2O3/TiO2 composite-modified fiber was characterized by field-emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and UV-visible spectroscopy. The synthesized composite exhibited notably high photocatalytic activity under visible light irradiation of λ up to 420 nm, whereby it could decompose organic pollutants in the aqueous and gaseous phases. Because of increasing environmental concerns, this photocatalytic system could be an important candidate for decomposing organic pollutants.

This paper describes the preparation of poly(vinyl alcohol)/kenaf fiber (PVOH/KF) composites with entrapped urea. The major FTIR peaks of these composites could be identified. These composites are intended for agricultural applications as biodegradable mulches and could be potential carrier materials for fertilizer. The water solubility, release behavior, chemical properties, and thermal stability of the composites were evaluated. The composites lost 25% of their weight after 7 days in water. In a wet environment, urea was released from the composites through its dissolution in water, and around 57% of the urea was released from the composites in 24 h; Thermagravimetric analysis showed that these composites were stable up 150 C. These composites would be able to withstand rain and protect seedlings from the sun when applied in the field as mulches. For around three to four weeks, these biobased mulches could slowly disintegrate as the PVOH binder was gradually dissolved by moisture, releasing the kenaf fibers to serve as soil fertilizer without leaving any undegradable waste for disposal. Hence, they would not pose any risks to the land or biological systems.

This work reported the thermomechanical and morphological properties of polyvinyl alcohol (PVA) nanocomposites reinforced with nanosilica and oil palm empty fruit bunches derived nanocellulose. The nanocomposites were characterized by mechanical, thermal, XRD, optical, and morphological studies. Uniformity dispersion of the nanofillers at a 3 wt% concentration has been shown by scanning electron microscopy, whereas the changes in crystallinity were demonstrated by X-ray diffraction analysis. Addition of nanosilica resulted in increased thermal stability of PVA/nanocellulose composites due to the reduction in mobility of the matrix molecules. Visible light transmission showed that the addition of 0.5 wt% nanosilica only slightly reduced the light transmission of PVA/nanocellulose composites with 3 wt% nanocellulose. The addition of a small concentration of nanosilica successfully improved the tensile and modulus properties of PVA/nanocellulose composite films. The increases in tensile strength and thermal stability were evidence of a nanosilica contribution in PVA/nanocellulose composites, inducing reinforcement, as detected by the thermomechanical properties.

The increase of environmental awareness has led to interest in the use of materials with eco-friendly attributes. In this study, a sandwich composite was developed from polyester and kenaf fiber with various orientation arrangements. Polyester/kenaf sandwich composite was fabricated through the combination of a hand lay-up process and cold compression. The tensile, flexural, and Izod impact tests of the sandwich composites were evaluated by using a universal tensile tester and an impact tester. The thermal stability of polyester/kenaf sandwich composite and plywood were investigated by using a thermogravimetric analyser. Results showed that the polyester/kenaf sandwich composite with kenaf fiber in anisotropy orientation achieved the highest mechanical properties. The kenaf fiber in anisotropic orientation could absorb the impact energy and allow the sandwich composite to withstand greater impact forces compared to composite with fiber in perpendicular or isotropic orientations. The polyester/kenaf sandwich composite also showed higher thermal stability compared to a conventional plywood sheet. Thus, the fabrication of polyester/kenaf sandwich composite with kenaf fiber in an anisotropic orientation design has great potential to replace plywood sheets for beam construction applications.

The physico-mechanical properties of lignocellulosic kenaf fiber reinforced polyvinyl alcohol (PVA) biocomposite films were investigated. To improve the properties of the biocomposite, kenaf fibers were chemically treated separately in a single stage (with Cr2(SO4)312(H2O)) and double stages (with CrSO4 and NaHCO3) to improve the adhesion and compatibility between the kenaf fiber and PVA matrix. PVA was reinforced with various compositions of chemically treated kenaf fiber by using a solution casting technique. Microstructural analyses and mechanical tests were subsequently conducted. Scanning electron microscopic analysis indicated that chemical treatment improved the uniformity distribution of kenaf fiber within the PVA matrix. FTIR and XRD analyses confirmed the presence of chromium on the fiber surface. The tensile strength of PVA reinforced with chemical treated kenaf fiber was found to be higher than those reinforced with untreated kenaf. The Young’s modulus, flexural strength, and flexural modulus increased with fiber loading for both untreated and treated kenaf fiber reinforced PVA films. The double stage treated kenaf fiber showed better mechanical properties and lower moisture uptake than the single stage treated kenaf fiber.

The effects of chlorite bleaching on the properties of cellulose derived from oil palm empty fruit bunch (OPEFB) fiber were investigated in this work. Cellulose was extracted from oil palm empty fruit bunch fiber via chlorite bleaching, alkali treatment, and acid hydrolysis. Cellulose was extracted by varying the bleaching duration, which corresponded to 4, 8, or 12 h. Fourier transform infrared (FTIR) analysis showed that the lignin and hemicellulose were significant removed after the bleaching process, whereas no spectral differences were observed in the samples with the increase of bleaching durations. The main removal of the lignin and hemicellulose components had occurred during the bleaching process. There was only slight additional removal of lignin and hemicellulose during the further extraction process with alkali and acid hydrolysis. The peaks at 1740 cm-1 and 1246 cm-1 which represent hemicellulose and lignin, respectively, were not present in the final extracted cellulose.The cellulose yield contents did not increase with the increasing of bleaching duration from 4 h to 12 h. X-ray diffraction (XRD) analysis revealed that the crystallinity and the 200 peak of OPEFB had increased after the bleaching process. Analysis of the visible light transmittance of cellulose, after a bleaching duration of 12 h, demonstrated the highest transmittance due to the disintegration of the fibers. By increasing the bleaching duration, the temperature at 50% weight loss of OPEFB increased, suggesting that the thermal stability of cellulose had improved.

Lignocellulosic fibers and lignin are two of the most important natural bioresources in the world. They show tremendous potential to decrease energy utilization/pollution and improve biodegradability by replacing synthetic fibers in bioplastics. The compatibility between the fiber-matrix plays an important part in the properties of the bioplastics. The improvement of lignocellulosic fiber properties by most surface treatments generally removes lignin. Due to the environmental pollution and high cost of cellulose modification, focus has been directed toward the use of lignocellulosic fibers in bioplastics. In addition, lignin-reinforced bioplastics are fabricated with varying success. These applications confirm there is no need to remove lignin from lignocellulosic fibers when preparing the bioplastics from a technical point of view. In this review, characterizations of lignocellulosic fibers and lignin related to their applications in bioplastics are covered. Then, we generalize the developments and problems of lignin-reinforced bioplastics and modification of lignin to improve the interaction of lignin-matrix. As for lignocellulosic fiber-reinforced bioplastics, we place importance on the low compatibility of the lignocellulosic fiber−matrix. The applications of lignin-containing cellulose and lignocellulosic fibers without delignification in the bioplastics are reviewed. A comparison between lignocellulosic fibers and lignin in the bioplastics is given.

Reinforcing polyoxymethylene (POM) with glass fibers (GF) enhances its mechanical properties, but at the expense of tribological performance. Formation of a transfer film to facilitate tribo-contact is compromised due to the abrasiveness of GF. As a solid lubricant, for example, polytetrafluoroethylene (PTFE) significantly improves friction and wear resistance. The effects of chemically etched PTFE micro-particles on the fiber-matrix interface of POM/GF/PTFE composites have not been systematically characterized. The aim of this study is to investigate their tribological performance as a function of micro-PTFE blended by weight percentage. Samples were prepared by different compositions of PTFE (0, 1.7, 4.0, 9.5, 15.0 and 17.3 wt.%). The surface energy of PTFE micro-particles was increased by etching for 10 min using sodium naphthalene salt in tetrahydrofuran. Tribological performance was characterized through simultaneous acquisition of the coefficient of friction and wear loss on a reciprocating test rig in accordance to Procedure A of ASTM G133-95. Friction and wear resistance improved as the micro-PTFE weight ratio was increased. Morphology analysis of worn surfaces showed transfer film formation, encapsulating the abrasive GF. Energy dispersive X-ray spectroscopy (EDS) revealed increasing PTFE concentration from the GF surface interface region (0.5, 1.0, 1.5, 2.0, 2.5 µm).

This paper investigated the effects of polytetrafluoroethylene (PTFE) micro-particles on mechanical properties of polyoxymethylene (POM) composites. Since PTFE is immiscible with most polymers, the surface was etched using sodium naphthalene salt in tetrahydrofuran to increase its surface energy. The effects of two variables, namely PTFE content and PTFE etch time, on the mechanical properties of the composite were studied. Experiments were designed in accordance to response surface methodology (RSM) using central composite design (CCD). Samples were prepared with different compositions of PTFE (1.7, 4.0, 9.5, 15.0, or 17.3 wt %) at different PTFE etch times (2.9, 5.0, 10.0, 15.0, or 17.1 min). Four mechanical properties of the POM/GF/PTFE composites, that is, strength, stiffness, toughness, and hardness, were characterized as a function of two studied variables. The dependency of these mechanical properties on the PTFE etch conditions was analyzed using analysis of variance (ANOVA). Overall desirability, D global index, was computed based on the combination of these mechanical properties for POM/GF/PTFE composites. The D global index was found to be 87.5%, when PTFE content and PTFE etch time were 6.5% and 10 min, respectively. Good correlation between experimental and RSM models was obtained using normal probability plots.

Non-isocyanate polyurethane (NIPU) was prepared from Jatropha curcas oil (JCO) and its alkyd resin via curing with different diamines. The isocyanate-free approach is a green chemistry route, wherein carbon dioxide conversion plays a major role in NIPU preparation. Catalytic carbon dioxide fixation can be achieved through carbonation of epoxidized derivatives of JCO. In this study, 1,3-diaminopropane (DM) and isophorone diamine (IPDA) were used as curing agents separately. Cyclic carbonate conversion was catalyzed by tetrabutylammonium bromide. After epoxy conversion, carbonated JCO (CJCO) and carbonated alkyd resin (CC-AR) with carbonate contents of 24.9 and 20.2 wt %, respectively, were obtained. The molecular weight of CJCO and CC-AR were determined by gel permeation chromatography. JCO carbonates were cured with different amine contents. CJCO was blended with different weight ratios of CC-AR to improve its characteristics. The cured NIPU film was characterized by spectroscopic techniques, differential scanning calorimetry, and a universal testing machine. Field emission scanning electron microscopy was used to analyze the morphology of the NIPU film before and after solvent treatment. The solvent effects on the NIPU film interfacial surface were investigated with water, 30% ethanol, methyl ethyl ketone, 10% HCl, 10% NaCl, and 5% NaOH. NIPU based on CCJO and CC-AR (ratio of 1:3) with IPDA crosslink exhibits high glass transition temperature (44 °C), better solvent and chemical resistance, and Young’s modulus (680 MPa) compared with the blend crosslinked with DM. Thus, this study showed that the presence of CC-AR in CJCO-based NIPU can improve the thermomechanical and chemical resistance performance of the NIPU film via a green technology approach.

Extensive employment of biomaterials in the areas of biomedical and microbiological applications is considered to be of prime importance. As expected, oil based polymer materials were gradually replaced by natural or synthetic biopolymers due to their well-known intrinsic characteristics such as biodegradability, non-toxicity and biocompatibility. Literature on this subject was found to be expanding, especially in the areas of biomedical and microbiological applications. Introduction of porosity into a biomaterial broadens the scope of applications. In addition, increased porosity can have a beneficial effect for the applications which exploit their exceptional ability of loading, retaining and releasing of fluids. Different applications require a unique set of pore characteristics in the biopolymer matrix. Various pore morphologies have different characteristics and contribute different performances to the biopolymer matrix. Fabrication methods for bio-based porous materials more related to the choice of material. By choosing the appropriate combination of fabrication technique and biomaterial employment, one can obtain tunable pore characteristic to fulfill the requirements of desired application. In our previous review, we described the literature related to biopolymers and fabrication techniques of porous materials. This paper we will focus on the biomedical and microbiological applications of bio-based porous materials.

A unique biodegradable, superporous, swellable and pH sensitive nanocellulose reinforced chitosan hydrogel with dynamic mechanical properties was prepared for oral administration of curcumin. Curcumin, a less water-soluble drug was used due to the fact that the fast swellable, superporous hydrogel could release a water-insoluble drug to a great extent. CO2 gas foaming was used to fabricate hydrogel as it eradicates using organic solvents. Field emission scanning electron microscope images revealed that the pore size significantly increased with the formation of widely interconnected porous structure in gas foamed hydrogels. The maximum compression of pure chitosan hydrogel was 25.9 ± 1 kPa and it increased to 38.4 ± 1 kPa with the introduction of 0.5% cellulose nanocrystals. In vitro degradation of hydrogels was found dependent on the swelling ratio and the amount of CNC of the hydrogel. All the hydrogels showed maximum swelling ratios greater than 300%. The 0.5% CNC-chitosan hydrogel showed the highest swelling ratio of 438% ± 11%. FTIR spectrum indicated that there is no interaction between drug and ingredients present in hydrogels. The drug release occurred in non-Fickian (anomalous) manner in simulated gastric medium. The drug release profiles of hydrogels are consistent with the data obtained from the swelling studies. After gas foaming of the hydrogel, the drug loading efficiency increased from 41% ± 2.4% to 50% ± 2.0% and release increased from 0.74 to 1.06 mg/L. The drug release data showed good fitting to Ritger-Peppas model. Moreover, the results revealed that the drug maintained its chemical activity after in vitro release. According to the results of this study, CNC reinforced chitosan hydrogel can be suggested to improve the bioavailability of curcumin for the absorption from stomach and upper intestinal tract.

Biopolymers and their applications have been widely studied in recent years. Replacing the oil based polymer materials with biopolymers in a sustainable manner might give not only a competitive advantage but, in addition, they possess unique properties which cannot be emulated by conventional polymers. This review covers the fabrication of porous materials from natural biopolymers (cellulose, chitosan, collagen), synthetic biopolymers (poly(lactic acid), poly(lactic-co-glycolic acid)) and their composite materials. Properties of biopolymers strongly depend on the polymer structure and are of great importance when fabricating the polymer into intended applications. Biopolymers find a large spectrum of application in the medical field. Other fields such as packaging, technical, environmental, agricultural and food are also gaining importance. The introduction of porosity into a biomaterial broadens the scope of applications. There are many techniques used to fabricate porous polymers. Fabrication methods, including the basic and conventional techniques to the more recent ones, are reviewed. Advantages and limitations of each method are discussed in detail. Special emphasis is placed on the pore characteristics of biomaterials used for various applications. This review can aid in furthering our understanding of the fabrication methods and about controlling the porosity and microarchitecture of porous biopolymer materials.

The properties of a composite material depend on its constituent materials such as natural biopolymers or synthetic biodegradable polymers and inorganic or organic nanomaterials or nano-scale minerals. The significance of bio-based and synthetic polymers and their drawbacks on coating film application is currently being discussed in research papers and articles. Properties and applications vary for each novel synthetic bio-based material, and a number of such materials have been fabricated in recent years. This review provides an in-depth discussion on the properties and applications of biopolymer-based nanocomposite coating films. Recent works and articles are cited in this paper. These citations are ubiquitous in the development of novel bionanocomposites and their applications.