Mangrove Oyster (Crassostrea belcheri) as a Biomonitor Species for Bioavailability of Polycyclic Aromatic Hydrocarbons (PAHs) from Sediment of the West Coast of Peninsular Malaysia

ABSTRACT

Rapid industrialization and urbanization in the west coast of Peninsular Malaysia has caused increasing pollution particularly of petroleum and petroleum by-products. Surface sediment and mangrove oyster (Crassostrea belcheri) were collected from five mangrove ecosystems in the west coast of Peninsular Malaysia and investigated for bioavailability of polycyclic aromatic hydrocarbons (PAHs). Sampling locations were selected from both remote areas with few or no previous records of petroleum pollution such as Pulau Merambong and polluted areas that are under international attention such as Klang mangrove ecosystem. PAH fractions were obtained through soxhlet extraction and two-step column chromatography and the fractions were injected to gas chromatography-mass spectrometry (GC-MS) for analysis. The concentrations of PAHs ranged from 151 to 4973 ng g^?1 dw in the sediments, while from 309 to 2225 ng g^?1 dw in the oysters. When tested for diagnostic ratios, a predominance of pyrogenic source PAHs was detected in the sediments, whereas PAHs in the oysters had mixed petrogenic and pyrogenic sources. A significant correlation (p < 0.05) was found between high molecular weight (HMW) PAHs in the sediments and oysters and biota accumulation factors (BAFs) of PAHs were approaching or exceeding unity indicating the ability of mangrove oyster in bioaccumulation of PAHs. Overall, this study indicates that mangrove oyster (C. belcheri) can be used as a biomonitor species for PAHs in an aquatic environment.     

MODELING OF MEMBRANE FOULING AND FLUX DECLINE IN MICROFILTRATION OF OILY WASTEWATER USING CERAMIC MEMBRANES

One of the major problems in pressure-driven membrane processes is reduction of flux far below the theoretical capacity of the membrane. The results of an experimental study of fouling mechanisms of ceramic membranes in separation of oil from synthesized oily wastewaters are presented. Mullite microfiltration (MF) membranes were synthesized from kaolin clay as MF ceramic membranes. The rejection of total organic carbon (TOC) for the synthetic feeds was found to be more than 94% by these membranes. Hermia's models were used to investigate the fouling mechanisms of membranes. The effect of pressure, cross flow velocity (CFV), temperature, oil concentration, and salt concentration on flux decline were investigated. The results showed that the cake filtration model can well predict the flux decline of mullite ceramic membranes; average error of this model is less than 7%. The results show that by increasing pressure from 0.5 to 4 bar, porosity of the cake layer on the mullite membranes decreases from 25.68% to 14.98%. After the cake filtration model, the intermediate pore blocking model was found to well predict the experimental data with an average error less than 10.5%.     

Study of Some Variables Affecting Particle Size and Particle Size Distribution of Suspension Polymerization of Methyl Methacrylate

A laboratory reactor was designed and constructed to study the effect of both speed of agitation and a concentration of suspension stabilizer on particle size and particle size distribution during the suspension polymerization of methyl methacrylate. It was concluded that the average particle size of the prepared polymer powder is directly proportional to the speed of agitation and is inversely proportional to the stabilizer concentration. New empirical equations correlating the average particle size and the particle size distribution (PSD) were derived from the study.     

Distributed model predictive control of switched nonlinear systems with scheduled mode transitions

A method for the design of distributed model predictive control (DMPC) systems for a class of switched nonlinear systems for which the mode transitions take place according to a prescribed switching schedule is presented. Under appropriate stabilizability assumptions on the existence of a set of feedback controllers that can stabilize the closed‐loop switched, nonlinear system, a cooperative DMPC architecture using Lyapunov‐based model predictive control (MPC) in which the distributed controllers carry out their calculations in parallel and communicate in an iterative fashion to compute their control actions is designed. The proposed DMPC design is applied to a nonlinear chemical process network with scheduled mode transitions and its performance and computational efficiency properties in comparison to a centralized MPC architecture are evaluated through simulations. © 2013 American Institute of Chemical Engineers AIChE J, 59:860‐871, 2013     

The component miscibility evolution during polymerization of the polybutadiene containing styrene solutions

In situ graft copolymerization of polystyrene (PS) on polybutadiene (PB) during polymerization of PB solution in styrene monomer was investigated to determine the performance of grafting process, chain structure of generated copolymers, and their effectiveness as compatibilizing agents for incompatible PS-rich and PB-rich phases. The amount of copolymers and their chain structures at different stages of polymerization were determined by gel permeation chromatography (GPC) curves of the reactive blends (taken directly from the reaction) and physical blends (physically prepared based on total composition of reactive blends). It was demonstrated that copolymer formation started from the early stage of polymerization and continued up to the phase inversion stage. In addition, PS grafting on PB occurred initially via single-chain attachment and then converted to a double-chain scenario later on. Compatibilizing efficiency of the copolymers was evaluated by Huggins coefficient (k _H) obtained by performing dilute solution viscometry (DSV) on samples taken at different stages of conversions. The effect of molecular weight of PB on the grafting process and the effectiveness of copolymers generated were also studied. It was found that while compatibilizing role of the copolymers produced from high molecular weight PB (HPB) increases as conversion goes further, the compatibilizing efficiency of the copolymers produced from low molecular weight PB (LPB) shows a very sharp variation in a small range of conversion. Plotting k _H of physical blends against weight fraction of PB molecules in solid content of the solutions (w _PB) showed negative deviation from mixture law with a W-like pattern containing two minima with a maximum in between. While a negative deviation was assumed as indication of immiscibility of the components, upward deviation at middle values of w _PB was attributed to molecular segregations that reduce the interface between the incompatible PS-rich and PB-rich phases.     

Fabrication and modification of polyvinylchloride based heterogeneous cation exchange membranes by simultaneously using Fe-Ni oxide nanoparticles and Ag nanolayer: Physico-chemical and antibacterial characteristics

Polyvinylchloride-blend-styrene butadiene rubber based nanocomposite cation exchange membranes were prepared by solution casting technique. Iron-oxide nanoparticles and Ag-nanolayer were simultaneously utilized as filler and surface modifier in membrane fabrication. The effects of Ag-nanolayer film thickness on membrane physicochemical and antibacterial characteristics of nanocomposite PVC-blend-SBR/Iron-oxide nanoparticles were studied. SEM images showed membrane roughness decreasing by Ag nanolayer thickness increasing. Membrane charge density and selectivity declined by Ag nanolayer coating up to 5 nm in membranes and then showed increasing trend by more nanolayer thickness. Ionic flux also showed increasing trend. Membranes showed good ability in E-Coli removal. 20 nm Ag-nanolayer coated membrane showed better performance compared to others.     

Nanostructure silver-doped zinc oxide films coating on glass prepared by sol–gel and photochemical deposition process: Application for removal of mercaptan

Silver-doped zinc oxide (SDZO) films have been grown on glass substrate by a novel combination of sol–gel and photochemical deposition processes (SGPD). The effect of sintering on structural, electrical and optical properties was investigated. The films were characterized by UV–vis absorption spectroscopy (UV–vis), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The result of X-ray photoelectron spectroscopy (XPS) revealed that the binding energy of Ag 3d_5/2 for SDZO shifts remarkably to the lower binding energy compared to the pure metallic Ag due to the interaction between silver and zinc oxide. The XRD spectra of the SDZO films indicate that silver was incorporated in the hexagonal crystal structure of zinc oxide. SEM micrographs show the uniform distribution of spherical grains of about 73 nm grain size for the pure zinc oxide thin films. The results indicated that silver doping photochemical deposition was a feasible method to tune the optical properties of zinc oxide nanostructures. SDZO films coated on glass were applied for the photodegradation of mercaptan in water. SDZO films were applied for degradation of mercaptobenzoxazole which reduced the mercaptan concentration to more than 98%.     

Experimental investigation of particle contact time at the wall of gas fluidized beds

The contact time of particles at the walls of gas fluidized beds has been studied using a radioactive particle tracking technique to monitor the position of a radioactive tracer. The solids used were sand or FCC particles fluidized by air at room temperature and atmospheric pressure at various superficial velocities, covering both bubbling and turbulent regimes of fluidization. Based on the analysis of tracer positions, the motion of individual particles near the walls of the fluidized bed was studied. The contact time, contact distance and contact frequency of the particles at the wall were evaluated from these experimental data. It was found that in a bed of sand particles, the mean wall contact time of the fluidized bed of sand particles decreases by increasing the gas velocity in the bubbling and increases in the turbulent fluidization. In other words, the particle-wall contact time is minimum at the onset of turbulent fluidization in the bed of sand particles. However, the mean wall contact time is almost constant in both regimes of fluidization in the bed of FCC particles. All the existing models in the literature predict a decreasing contact time when the gas velocity in the bed is increased. It was also shown that the contact distance increases monotonously by increasing the gas velocity in the bed of sand particles, while it is almost constant for the bed of FCC particles. Contact frequency has a trend similar to that of the contact time for both sand and FCC particles.     

Synergistic effect of salt ions and water-soluble amphiphilic compounds of acidic crude oil on surface and interfacial tension

This study investigated the effect of solubility of amphiphilic compounds of acidic crude oil in water on the surface and interfacial tension (IFT) with NaCl, MgCl₂, CaCl₂, and Na₂SO₄ salts. Accordingly, distilled water, along with the salts mentioned in zero ionic strength up to 2 mol were put in contact with crude oil to become saturated with amphiphilic compounds. The effects of these compounds were investigated on the properties of contact water by pH, total organic carbon (TOC), FTIR (Fourier transform infrared spectroscopy), water-air surface tension (ST), and water-n-decane IFT tests. The results showed that some of the organic components of crude oil, especially acidic and basic compounds, are present or soluble in water, which have a significant effect on reducing the surface and IFT. The IFT reduction of water-n-decane was greater than the water-air ST system. Also, the observations showed that for both NaCl and Na₂SO₄ salt water, with increasing ionic strength of water, there was an optimum salinity within the range of 0.1-0.25 mol/L for both salts with the amount of surface and IFT minimized at this point. In the other two salts, this point was delayed upon elevation of ionic strength and was observed at high salinity. In this case, divalent cations reduce tension rate compared to monovalent cations. Due to solubility of acidic and basic groups in water, pH of salt water illustrates an acidic trend. Results of the FTIR test confirmed solubility of these compounds as well.