Advanced technology in petrochemical-based polymer has brought many benefits to mankind. However, the use of nonbiodegradable plastics materials for disposable application such as food packaging and house whole appliances are significantly disturbing and damaging the earth ecosystem. Polylactic acid (PLA) is a biodegradable plastic that is brittle. Because of this nature, PLA has a limitation in its usage. The common way to improve the toughness of PLA is via adding plasticizer. This review will provide brief account on recent developments in the synthesis of lactic acid (monomer of PLA) through biological route, PLA synthesis, unique material properties of PLA and modification of those by making copolymers and composites PLA absorption and degradation
Covalently cross-linked nanogels were prepared via irradiation of inverse micelles that had been preparedfrom radiation crosslinkable polymer, water, oil and surfactant. A mixture of polymer, water, heptane andsodium dioctyl sulfosuccinate (AOT) at certain compositions forms inverse micelles with the size rangingfrom 2 to 8 nm. The hydrophilic head of the surfactant facilitates encapsulation of water soluble polymer.If the entrapped polymer is radiation crosslinkable, it is expected that upon irradiation, polymerizationshall take place in such small and confined space, leading to formation of nano-sized polymeric gel.Meanwhile, emulsion at 2 nm size was chosen for gamma irradiation process. The formation of thenano-sized discreet gel using irradiation of inverse micelles technique was proven at a dose as low as 5kGy to obtain nanogel sized ~ 95 nm.
Poly(hydroxamic acid) ion exchange resin was evaluated for speciation of iron(II) and iron(III) ions. Distribution coefficients indicate that the resin is more selective towards iron(III) ion. Column extractions show that iron(III) ion is quantatively extracted from sulfuric acid solutions at concentrations of between 0.01 to 0.00lM but only 2% or less of iron(II) ion is retained under these conditions. Further studies show that these two ions can be separated and their separations are not affected by the presence of nickel, zinc, copper, calcium, chloride, bromide, nitrate and sulphate.
Resin penukar ion poli(asid hidroksamik) telah dikaji untuk penspesiesan ion-ionferum. Pekali taburan menunjukkan resin ini mempunyai kepilihan yang tinggi terhadap ion ferik berbanding dengan ionferus. Pengekstrakan dengan kaedah turus mendapati ion ferik dari larutan asid sulfurik 0.01 dan 0.00lM boleh diesktrak secara kuantitatif manakala pengekstrakan ion ferus hanya 2% atau lebih kecil. Kajian lanjut menunjukkan resin ini boleh memisahkan ion ferik dari ion ferus dan pemisahan ini tidak diganggu oleh kehadiran ion-ion nikel, zink, kuprum, kalsium, klorida, bromida, nitrat dan sulfat.
This review summarizes the evolution that has been made for organophosphates (OPs) detection technique using conventional technique (lab-based) and compact technique (colorimetric and electrochemical). Right after introduction section, a first section covers the types, chemical structure and risks of OPs. Methods for detection using conventional and compact technique were discussed next. An additional section covers the limitation of conventional detection technique and advantages of compact detection technique are addressed. Several Tables are presented that give an overview on the OPs detection using conventional and compact detection technique. A concluding section addresses a brief idea on the detection method available nowadays.
Epoxidized fatty hydrazides (EFHs) which have amine, amide and epoxide functional groups in their molecules are a versatile starting material for synthesizing of many industrially important compounds. In this report we describe the results of our preliminary study of synthesizing these compounds using a chemical reaction of epoxidized palm olein (EPO) and hydrazine monohydrate. The products were characterized by using Fourier transform infrared (FTIR) spectroscopy, nuclear magnetic resonance (NMR) technique and CHN elemental analyser. The optimum reaction conditions for the hydrazide preparation were investigated by studying effect of each important reaction parameters on the product yields. The study shows that the optimum conditions to produce EFHs were using EPO to hydrazine monohydrate (mol ratio of 1 to 12), n-hexane as the solvent and at the temperature of 69 ̊C.
Poly(lactic acid) (PLA)-based nanocomposites filled with graphene nanoplatelets (xGnP) that contains epoxidized palm oil (EPO) as plasticizer were prepared by melt blending method. PLA was first plasticized by EPO to improve its flexibility and thereby overcome its problem of brittleness. Then, xGnP was incoporated into plasticized PLA to enhance its mechanical properties. Plasticized and nanofilled PLA nanocomposites (PLA/EPO/xGnP) showed improvement in the elongation at break by 3322% and 61% compared to pristine PLA and PLA/EPO, respectively. The use of EPO and xGnP increases the mobility of the polymeric chains, thereby improving the flexibility and plastic deformation of PLA. The nanocomposites also resulted in an increase of up to 26.5% in the tensile strength compared with PLA/EPO blend. XRD pattern showed the presence of peak around 26.5° in PLA/EPO/xGnP nanocomposites which corresponds to characteristic peak of graphene nanoplatelets. Plasticized PLA reinforced with xGnP showed that increasing the xGnP content triggers a substantial increase in thermal stability. Crystallinity of the nanocomposites as well as cold crystallization and melting temperature did not show any significant changes upon addition of xGnP. However, there was a significant decrease of glass transition temperature up to 0.3wt% of xGnP incorporation. The TEM micrograph of PLA/EPO/xGnP shows that the xGnP was uniformly dispersed in the PLA matrix and no obvious aggregation was observed.
An artificial neural network (ANN) was applied for the determination of V(V) based on immobilized fatty hydroxamic acid (FHA) in poly(methyl methacrylate) (PMMA). Spectra obtained from the V(V)-FHA complex at single wavelengths was used as the input data for the ANN. The V(V)-FHA complex shows a limited linear dynamic range of V(V) concentration of 10 - 100 mg/ L. After training with ANN, the linear dynamic range was extended with low calibration error. A three layer feed forward neural network using backpropagation (BP) algorithm was employed in this study. The input layer consisted of single neurons, 30 neurons in hidden a layer and one output neuron was found appropriate for the multivariate calibration used. The network were trained up to 10000 epochs with 0.003 % learning rate. This reagent also provided a good analytical pedormance with reproducibility characters of the method yielding relative standard deviation (RSD) of 9.29% and 7.09% for V(V) at concentrations of 50 mg/ L and 200 mg/ L, respectively. The limit of detection of the method was 8.4 mg/ L.
Synthesis of palm oil based-urethane acrylate (POBUA) resins was carried out by acrylation of epoxidizedpalm oil (EPOP) using acrylic acid in the presence of a catalyst and followed by isocyanation to obtainthe POBUA. Using the monomer as a diluent in the formulation, 4% of photoinitiator and incorporationof organoclay (1-5% wt), nanocomposites were obtained upon UV irradiation. The X-ray DiffractoryXRD study revealed that the nanocomposites obtained were of the exfoliation type. The presence ofthe clay improved the hardness and did not affect the thermal stability. Similarly, it increased the glasstransition temperature Tg but reduced the modulus as the clay content was increased. The improvementof the tensile strength was only obtained when the clay concentration was 5 phr.
Effects of organoclay concentration on the properties of radiation crosslinked natural rubber (NR)/ ethylene vinyl acetate (EVA)/clay nanocomposites were investigated. The NR/EVA blend with a ratio of 40/60 was melt blended with different concentration of either dodecyl ammonium montmorillonite (DDA-MMT) or dimethyl dihydrogenated tallow quarternary ammonium montmorillonite (C20A). Composite of NR/EVA blend with unmodified clay (Na-MMT) was also prepared for comparison purposes. The composites were irradiated with electron beam (EB) at an optimum irradiation dose. The formation of radiation-induced crosslinking depends on the type and concentration of the organoclay used in the preparation of nanocomposites as measured by gel content. Changes in the interlayer distance of the silicate layers with the increase of organoclay concentration were shown by the XRD results. Variation in the tensile properties of the nanocomposites with the increase of organoclay concentration depends on the formation of crosslinking as well as reinforcement effect of the organoclay. Improvement in thermal stability of the NR/EVA blend was also observed with the presence of organoclay.
The use of microemulsion in the development of nanoparticle based on acrylated palm oil product is demonstrated. Acr ylated palm oil microemulsions were prepared using ionic surfactant. Combination methods of emulsion polymerization and radiation crosslinking were applied to the microemulsion system for synthesizing nanoparticle. The ionizing radiat ion technique was introduced to generate a crosslinking reaction in the development of nanoparticle. The nanoparticle was evaluated in terms of particle diameter, surface charge, pH and conductance. Their image was captured using Tra nsmission electron microscopy (TEM). Results show that the size, charge and shape of the particles are influenced by c oncentration of surfactants, monomer concentration, radiation dose and time of storage. The study showed a promising method to produced nanoparticle. This nano-sized product has the potential to be utilized as controlled-drug-release-carrier.