Mohamad Zaki Ab. Rahman

Synthesis, surface modification and characterisation of biocompatible magnetic iron oxide nanoparticles for biomedical applications.

Superparamagnetic iron oxide nanoparticles (MNPs) with appropriate surface chemistry exhibit many interesting properties that can be exploited in a variety of biomedical applications such as magnetic resonance imaging contrast enhancement, tissue repair, hyperthermia, drug delivery and in cell separation. These applications required that the MNPs such as iron oxide Fe3O4 magnetic nanoparticles (Fe3O4 MNPs) having high magnetization values and particle size smaller than 100 nm. This paper reports the experimental detail for preparation of monodisperse oleic acid (OA)-coated Fe3O4 MNPs by chemical co-precipitation method to determine the optimum pH, initial temperature and stirring speed in order to obtain the MNPs with small particle size and size distribution that is needed for biomedical applications. The obtained nanoparticles were characterized by Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy dispersive X-ray fluorescence spectrometry (EDXRF), thermogravimetric analysis (TGA), X-ray powder diffraction (XRD), and vibrating sample magnetometer (VSM). The results show that the particle size as well as the magnetization of the MNPs was very much dependent on pH, initial temperature of Fe2+ and Fe3+ solutions and steering speed. The monodisperse Fe3O4 MNPs coated with oleic acid with size of 7.8 ± 1.9 nm were successfully prepared at optimum pH 11, initial temperature of 45 °C and at stirring rate of 800 rpm. FTIR and XRD data reveal that the oleic acid molecules were adsorbed on the magnetic nanoparticles by chemisorption. Analyses of TEM show the oleic acid provided the Fe3O4 particles with better dispersibility. The synthesized Fe3O4 nanoparticles exhibited superparamagnetic behavior and the saturation magnetization of the Fe3O4 nanoparticles increased with the particle size.

Sugar palm (Arenga pinnata): Its fibres, polymers and composites

Sugar palm (Arenga pinnata) is a multipurpose palm species from which a variety of foods and beverages, timber commodities, biofibres, biopolymers and biocomposites can be produced. Recently, it is being used as a source of renewable energy in the form of bio-ethanol via fermentation process of the sugar palm sap. Although numerous products can be produced from sugar palm, three products that are most prominent are palm sugar, fruits and fibres. This paper focuses mainly on the significance of fibres as they are highly durable, resistant to sea water and because they are available naturally in the form of woven fibre they are easy to process. Besides the recent advances in the research of sugar palm fibres and their composites, this paper also addresses the development of new biodegradable polymer derived from sugar palm starch, and presents reviews on fibre surface treatment, product development, and challenges and efforts on properties enhancement of sugar palm fibre composites.

Enhancement of Mechanical and Thermal Properties of Polycaprolactone/Chitosan Blend by Calcium Carbonate Nanoparticles

This study investigates the effects of calcium carbonate (CaCO3) nanoparticles on the mechanical and thermal properties and surface morphology of polycaprolactone (PCL)/chitosan nanocomposites. The nanocomposites of PCL/chitosan/CaCO3 were prepared using a melt blending technique. Transmission electron microscopy (TEM) results indicate the average size of nanoparticles to be approximately 62 nm. Tensile measurement results show an increase in the tensile modulus with CaCO3 nanoparticle loading. Tensile strength and elongation at break show gradual improvement with the addition of up to 1 wt% of nano-sized CaCO3. Decreasing performance of these properties is observed for loading of more than 1 wt% of nano-sized CaCO3. The thermal stability was best enhanced at 1 wt% of CaCO3 nanoparticle loading. The fractured surface morphology of the PCL/chitosan blend becomes more stretched and homogeneous in PCL/chitosan/CaCO3 nanocomposite. TEM micrograph displays good dispersion of CaCO3 at lower nanoparticle loading within the matrix.

Preparation and characterization of poly(2-acrylamido-2-methylpropane-sulfonic acid) grafted chitosan using potassium persulfate as redox initiator

A grafted material based on chitosan and 2-acrylamido-2-methylpropanesulfonic acid (AMPS) has been successfully prepared in homogenous solution using potassium persulfate as a redox initiator. The grafted copolymer was precipitated during the reaction polymerization. The effects of the reaction temperature and chitosan–potassium persulfate contact time as well as concentrations of AMPS, potassium persulfate, and acetic acid on grafting yield were investigated. The percentage of grafting is gradually increased with the increasing of the AMPS concentration. The extent of grafting can be controlled by setting the appropriate reaction conditions. The maximum percentage of grafting was about 180% under the optimum conditions (1% v/v acetic acid, 50°C reaction temperature, 10 min chitosan–potassium persulfate mixing period, 0.37 mmol of potassium persulfate, and 28.96 mmol AMPS). The grafted chitosan was insoluble in the acid of the grafting.

Synthesis and characterization of poly(hydroxamic acid) chelating resin from poly(methyl acrylate)-grafted sago starch

A new chelating ion-exchange resin containing the hydroxamic acid functional group was synthesized from poly(methyl acrylate) (PMA)-grafted sago starch. The PMA grafted copolymer was obtained by a free-radical initiating process in which ceric ammonium nitrate was used as an initiator. Conversion of the ester groups of the PMA-grafted copolymer into hydroxamic acid was carried out by treatment of an ester with hydroxylamine in an alkaline solution. The characterization of the poly(hydroxamic acid) chelating resin was performed by FTIR spectroscopy, TG, and DSC analyses. The hydroxamic acid functional group was identified by infrared spectroscopy. The chelating behavior of the prepared resin toward some metal ions was investigated using a batch technique. The binding capacities of copper, iron, chromium, and nickel were excellent and the copper capacity was maximum (3.46 mmol g−1) at pH 6. The rate of exchange of the copper ion was very fast that is, t1/2 Fe3+ > Cr3+ > Ni2+ > Co2+ > Zn2+ > Cd2+ > As3+ > Pb2+.

Comparative study of physical properties based on different parts of sugar palm fibre reinforced unsaturated polyester composites

This research was conducted to evaluate the potential of sugar palm residue as a raw material to produce the new green composites. The physical properties of sugar palm fibre reinforced unsaturated polyester composites from different part which are sugar palm frond (SPF/PE), sugar palm bunch (SPB/PE), sugar palm trunk (SPT/PE) and black sugar palm fibre (ijuk/PE) were studied. Samples were submerged in distilled water for 24 hours. The water absorption and thickness swelling were investigated in order to determine the dimensional stability of the composites. It is found that SPF/PE showed the higher value of water absorption and thickness swelling which are 1.57%, and 1.56% followed by SPB/PE (1.35%, 1.11%), ijuk/PE (0.65%, 0.76%) and SPT/PE (0.39%, 0.50%). Generally, this investigation is valuable for researchers in order to evaluate the potential and some possible application of sugar palm residues as a new natural composites product.

Enhancement of Mechanical and Thermal Properties of Oil Palm Empty Fruit Bunch Fiber Poly(butylene adipate-co-terephtalate) Biocomposites by Matrix Esterification Using Succinic Anhydride

In this work, the oil palm empty fruit bunch (EFB) fiber was used as a source of lignocellulosic filler to fabricate a novel type of cost effective biodegradable composite, based on the aliphatic aromatic co-polyester poly(butylene adipate-co-terephtalate) PBAT (EcoflexTM), as a fully biodegradable thermoplastic polymer matrix. The aim of this research was to improve the new biocomposites’ performance by chemical modification using succinic anhydride (SAH) as a coupling agent in the presence and absence of dicumyl peroxide (DCP) and benzoyl peroxide (BPO) as initiators. For the composite preparation, several blends were prepared with varying ratios of filler and matrix using the melt blending technique. The composites were prepared at various fiber contents of 10, 20, 30, 40 and 50 (wt %) and characterized. The effects of fiber loading and coupling agent loading on the thermal properties of biodegradable polymer composites were evaluated using thermal gravimetric analysis (TGA). Scanning Electron Microscopy (SEM) was used for morphological studies. The chemical structure of the new biocomposites was also analyzed using the Fourier Transform Infrared (FTIR) spectroscopy technique. The PBAT biocomposite reinforced with 40 (wt %) of EFB fiber showed the best mechanical properties compared to the other PBAT/EFB fiber biocomposites. Biocomposite treatment with 4 (wt %) succinic anhydride (SAH) and 1 (wt %) dicumyl peroxide (DCP) improved both tensile and flexural strength as well as tensile and flexural modulus. The FTIR analyses proved the mechanical test results by presenting the evidence of successful esterification using SAH/DCP in the biocomposites’ spectra. The SEM micrograph of the tensile fractured surfaces showed the improvement of fiber-matrix adhesion after using SAH. The TGA results showed that chemical modification using SAH/DCP improved the thermal stability of the PBAT/EFB biocomposite.

OPTICAL BAND GAP AND CONDUCTIVITY MEASUREMENTS OF POLYPYRROLE-CHITOSAN COMPOSITE THIN FILMS

Electrical conductivity and optical properties of polypyrrole-chitosan (PPy-CHI) conducting polymer composites have been investigated to determine the optical transition characteristics and energy band gap of composite films. The two electrode method and I–V characteristic technique were used to measure the conductivity of the PPy-CHI thin films, and the optical band gap was obtained from their ultraviolet absorption edges. Depending upon experimental parameter, the optical band gap (Eg) was found within 1.30–2.32 eV as estimated from optical absorption data. The band gap of the composite films decreased as the CHI content increased. The room temperature electrical conductivity of PPy-CHI thin films was found in the range of 5.84 × 10−7–15.25 × 10−7 S·cm−1 depending on the chitosan content. The thermogravimetry analysis (TGA) showed that the CHI can improve the thermal stability of PPy-CHI composite films.

Synthesis and mesomorphic properties of nonsymmetric liquid crystalline dimers containing azobenzene groups

Four novel nonsymmetric dimers containing azobenzene mesogenic groups were synthesized. The nonsymmetric dimers compounds namely, ethyl 4-[(4-{4-(4-((4-nitrophenyl)diazenyl)phenoxy)alkyloxy}phenyl)diazenyl]benzoate were obtained from the alkylation of ethyl 4-[(4-(4-bromoalkyloxy)phenyl)diazenyl]benzoate with 4-[(4-nitrophenyl)diazenyl]phenol. The mesomorphic properties of the compounds were determined by DSC and polarizing optical microscopy. The first member of the series was nonliquid crystalline while all other homologues display nematic and smectic A phases. The trans-azobenzene groups of the dimers display a high-intensity π–π* transition at about 365 nm and a low-intensity n–π* transition at around 465 nm, therefore, photochromism can be achieved by the introduction of the azo linkage to the dimeric liquid crystalline molecules.

Investigation on bending strength and stiffness of sugar palm fibre from different parts reinforced unsaturated polyester composites.

This investigation is done to select the best composite on bending strength and stiffness derived from different parts of sugar palm fibre reinforced unsaturated polyester composites. Sugar palm tree is one of the most popular natural fibres. The fibre was obtained from the sugar palm tree and mixed with unsaturated polyester (PE). All of the composites are labelled as SPF/PE for sugar palm frond composite, SPB/PE for sugar palm bunch composite, SPT/PE for sugar palm trunk composite and ijuk/PE for black sugar palm fibre composite. The bending strength and stiffness tests were done according to ASTM D 790-(2000). The higher value of bending strength and stiffness obtained by SPT/PE which is 41.906 MPa and 3.363 GPa respectively followed by SPF/PE (38.906 MPa and 3.001 GPa), SPB/PE (35.168 MPa and 2.749) and ijuk/PE (33.742 MPa and 2.424 GPa)