Acrylated palm oil nanoparticle synthesized by radiation-induced process as a controlled drug delivery system

The acrylated palm oil (APO) nanoparticle is a potential product that can be used as carriers in medical field. The main focus of the present study was to study the potential of the APO nanoparticles for used in a controlled drug delivery system. The microemulsion system is used as a medium to incorporate an active substance such as Thymoquinone (TQ) into the APO polymeric micelle and then the radiation technique is used as a tool for the synthesis of TQ-loaded APO nanoparticle. The nano-size TQ-loaded APO particles resulted the particle size of less than 150 nm with spherical in shape. The TQ release profile was carried out in potassium buffer saline (PBS) solutions (pH 7.4) at 37°C. And, the zero-order model has been used to determine the mechanism of the drug release from the corresponding nanoparticles, respectively. The TQ release was found to be sustained and controlled in pH 7.4. At pH 7.4, the release of TQ followed the zero-order model. The in-vitro drug release study showed a good prospect of the APO nanoparticle on being a potential drug carrier as there are toxic against colon cancer cells and not toxic towards normal cells. This suggested that the APO product produce using this radiation technique can be developed into different type of carrier systems for controlled drug release applications

Producing Jatropha oil-based polyol via epoxidation and ring opening

A low viscosity polyol has been functionalized from crude Jatropha oil via epoxidation and subsequent ring-opening. Starting with the crude Jatropha oil, the double bonds are functionalized by introducing epoxy groups and ring-opened to produce hydroxyl groups. The experiment employs more concentrated 50% hydrogen peroxide and effectively produce solvent-free epodixidized Jatropha oil within shorter reaction time of 5 h with maximum oxirane oxygen content of 4.30% and viscosity of 0.57–0.60 Pa.s. The epoxidized Jatropha oil is then transform into Jatropha-based polyol with hydroxyl number of 171–179 mg KOH/g, low viscosity of 0.92–0.98 Pa.s. and functionality of 5.1–5.3. The epoxidation and ring-opening process are monitored by viscometer and FTIR. The produced polyol permit more time for molding and additives addition during polyurethane due to its low viscosity

Radiation-induced formation of acrylated palm oil nanoparticle using pluronic F-127 microemulsion system

This study demonstrated the utilization of radiation-induced initiator methods for the formation of nanoparticles of Acrylated Palm Oil (APO) using aqueous Pluronic F-127 (PF-127) microemulsion system. This microemulsion system was subjected to gamma irradiation to form the crosslinked APO nanoparticles. Dynamic light scattering (DLS), Fourier Transform Infrared (FTIR) spectroscopy and Transmission Electron Microscopy (TEM) were used to characterize the size and the chemical structure of the nanoparticles. As a result, the size of the APO nanoparticle was decreased when the irradiation dose increased. The decrease in size might be due to the effects of intermolecular crosslinking and intramolecular crosslinking reactions of the APO nanoparticles during irradiation process. The size of the nanoparticle is in the range of 98 to 200 nanometer (nm) after irradiation using gamma irradiator. This radiation-induced method provides a free initiator induced and easy to control process as compared to the classical or chemical initiator process. The study has shown that radiation-induced initiator methods, namely, polymerization and crosslinking in the microemulsion, were promising for the synthesis of nanoparticles

Soil burial biodegradation studies of palm oil-based UV-curable films

The palm oil-based ultraviolet (uv)-curable films were subjected to an outdoor soil burial test to investigate the biodegradation under natural environment. The films were burial in the soil experiment plot at the Nuclear Malaysia’s Dengkil complex. The uv-curable films were synthesized from the epoxidized palm oil acrylated (EPOLA) resin and the polyurethane palm oil (POBUA) resin, respectively. Biodegradation tests are more specific to burial film in soil experiments for 12 months under natural conditions. The biodegradability of palm oil resin based uv-curable films were investigated and compared with the petrochemical resin based film. The films properties were compared with respect to properties of the thermal characteristic, the crystallinity, the morphology and the weight loss which are analyzed using the thermogravimetric analysis (TGA), the differential scanning calorimetry (DSC), the scanning electron microscope (SEM), an optical microscope and the weight loss of film calculation. These findings suggested that the palm oil-based uv-curable films show quite satisfactory biodegradation levels

Synthesis and Characterization UV-Curable Waterborne Polyurethane Acrylate/Al₂O₃ Nanocomposite Coatings Derived from Jatropha Oil Polyol

A new UV-curable waterborne polyurethane acrylate/alumina (UV-WPUA/Al₂O₃) coatings were successfully developed. The waterborne polyurethane acrylate (WPUA) dispersion was synthesized by reacting jatropha oil polyol (JOL) with isochrone diisocyanate (IPDI), 2,2-dimethylol propionic acid (DMPA), and 2-hydroxyethyl methacrylate (HEMA) via in-situ and anionic self-emulsifying methods. The WPUA/Al₂O₃ dispersion was formulated by various sonicating concentrations of alumina nanoparticles (0.3, 0.6, 0.9, and 1.2 wt%) into WPUA dispersion. The UVWPUA/Al₂O₃ coatings were obtained with 75 wt% oligomers, 25 wt% monomer trimethylolpropane triacrylate (TMPTA), and 3 wt% of a commercial photo initiator (benzhophenol) for UV-curing were used. The effect of Al₂O₃ nanoparticles on WPUA coatings was analyzed by FTIR, surface morphology, and coating performance properties such as pendulum hardness, pencil hardness, scratch resistance, and adhesion test. FTIR revealed the formation of JOL, neat UV-WPUA, and UV-WPUA/Al₂O₃ coatings, respectively. FESEM/EDX demonstrated that Al₂O₃ nanoparticles at the lower loading (up to 0.6 wt%) were well-dispersed correlated with contact angle (CA). The hardness property can reach 63.4% at the lower concentration of the Al₂O₃ addition 0.6 wt%. The adhesive strength, scratch hardness, and scratch resistance were greatly improved to 5B, 5H, and 2N, respectively. The preparation method offered in this study is an effective and convenient approach to producing UV-WPUA/Al₂O₃ coatings. The enhancement of the properties with the lesser concentration of Al₂O3 nanoparticles (≤ 0.6 wt%) addition in this study shows a new promising potential as surface coating application for several major industrial areas, such as marine, transportation, and biomedical field with major economic and environmental benefits

Colloidal stability and rheology of jatropha oil-based waterborne polyurethane (JPU) dispersion

Jatropha oil-based waterborne polyurethane (JPU) dispersions were produced by polymerising the jatropha oil-based polyols (JOLs) with isophrene diisocyanate (IPDI) and dimethylol propionic acid (DMPA). The colloidal stability of the resulting JPU dispersions were studied by particle size analysis and rheology measurements. Inclusion of up to 5.4 wt.% of DMPA as an internal emulsifier produced a wide range of particle sizes from 84 nm to 825 nm. The dispersions have a solid content of 24.2–26.9 wt.% with a relatively low viscosity in the range 6.2–60.2 mPa s. The JPU dispersions exhibited the typical flow behaviour of the commercial polyurethane dispersions, ranging from almost Newtonian to a shear thinning fluid, and the experimental data correlated well with the Cross model. The samples were stable after 18 months of storage under room conditions

Physico-chemical characterisation of epoxy acrylate resin from jatropha seed oil

Purpose: This paper aims to demonstrate the synthesis of polyesterification reaction of non-edible jatropha seed oil (JO) and acrylic acid, which leads to the production of acrylated epoxidised-based resin. To understand the physico-chemical characteristics when synthesis the JO-based epoxy acrylate, the effect of temperature on the reaction, concentration of acrylic acid and role of catalyst on reaction time and acid value were studied. Design/methodology/approach: First, the double bond in JO was functionalised by epoxidation using the solvent-free performic method. The subsequent process was acrylation with acrylic acid using the base catalyst triethylamine and 4-methoxyphenol as an inhibitor respectively. The physico-chemical characteristics during the synthesis of the epoxy acrylate such as acid value was monitored and analysed. The formation of the epoxy and acrylate group was confirmed by a Fourier transform infrared spectroscopy spectra analysis and nuclear magnetic resonance analysis. Findings: The optimum reaction condition was achieved at a ratio of epoxidised JO to acrylic acid of 1:1.5 and the reaction temperature of 110°C. This was indicated by the acid value reduction from 86 to 15 mg KOH/g sample at 6 hours. Practical implications: The JO-based epoxy acrylate synthesised has a potential to be used in formulations the prepolymer resin for UV curable coating applications. The JO which is from natural resources and is sustainable raw materials that possible reduce the dependency on petroleum-based coating. Originality/value: The epoxidised jatropha seed oil epoxy acrylate was synthesised, as a new type of oligomer resin that contains a reactive acrylate group, which can be alternative to petroleum-based coating and can used further in the formulation of the radiation curable coating

Chemical and Thermo-Mechanical Properties of Waterborne Polyurethane Dispersion Derived from Jatropha Oil

Nowadays, there is a significant trend away from solvent-based polyurethane systems towards waterborne polyurethane dispersions due to government regulations requiring manufacturers to lower total volatile organic compounds, as well as consumer preference for more environmentally friendly products. In this work, a renewable vegetable oil-based polyol derived from jatropha oil was polymerized with isophorone diisocyanate and dimethylol propionic acid to produce anionic waterborne polyurethane dispersion. Free standing films with up to 62 wt.% bio-based content were successfully produced after evaporation of water from the jatropha oil-based waterborne polyurethane (JPU) dispersion, which indicated good film formation. The chemical and thermomechanical properties of the JPU films were characterized. By increasing the OH numbers of polyol from 161 mgKOH/g to 217 mgKOH/g, the crosslinking density of the JPU was significantly increased, which lead to a better storage modulus and improved hydrophobicity. Overall, JPU produced from polyol having OH number of 217 mgKOH/g appears to be a promising product for application as a binder for wood and decorative coatings

Understanding intrinsic plasticizer in vegetable oil-based polyurethane elastomer as enhanced biomaterial

Renewable polyol is of increasing interest as a building block in biomedical elastomer for bearing biodegradable ester group and immaculate functionality. Derived from non-edible vegetable oil, a new class of elastomer was successfully functionalized with MDI and TDI. Crosslink densities were varied by regulating ratio of hydroxyl to diisocyanate (r) at 1/1.0, 1/1.1, and 1/1.2. Produced elastomers were examined by crosslink density, attenuated total reflectance Fourier transform infrared spectroscopy, differential scanning calorimetry, thermogravimetric analysis, dynamic mechanical analysis, tensile testing, and scanning electron microscopy. The obtained elastomers had subambient glass transition temperature (T g) suggested majority soft segment that acted as a continuous phase with intermediate phase separation. Medium conversion at gel point had enhanced physical properties. Highly elastic mechanical behavior was afforded from combination of side chains and high molecular weight polyol. At r = 1/1.2, MDI-based elastomer showed twofold improvement in Young modulus at slight expense of elongation. TDI-based elastomer accomplished elongation beyond 162%. Branching allophanate and biuret resisted early thermal breakdown by elevating activation energy. Frequency response and kinetic of thermal degradation provided beneficial perspective for elastomer characterization. The vegetable oil-based polyurethane was found able to resemble most of the physical properties of polycaprolactone (PCL)-derived polyurethane

Assessment of corrosion protection and performance of bio-based polyurethane acrylate incorporated with nano zinc oxide coating

In this study, a series of UV-curable anticorrosive PUA coatings embedded with varying concentrations of inorganic ZnO fillers have been successfully prepared from jatropha-based polyol. The electrochemical impedance spectroscopy (EIS) and Tafel polarisation analysis revealed that increasing fillers composition lead to the improvement of the anticorrosive property of the hybrid coatings. Meanwhile, the salt spray test results were found to correlate with the EIS of Cc (F cm−2) was 2.71 × 10−9, Bode plot - 106 Ω cm2 and Tafel polarisation results 7.56 × 10−6 MPY at 3 wt% of ZnO. Physical properties of 3 wt% loading of ZnO fillers in hardness test obtained 6H which was strongly attributed to the low interfacial interaction and poor dispersion of the fillers within the polymer matrix