The Thermal Performance Analysis of an Al2O3-Water Nanofluid Flow in a Composite Microchannel.

Partial filling of porous medium insert in a channel alleviates the tremendous pressure drop associated with a porous medium saturated channel, and enhances heat transfer at an optimum fraction of porous medium filling. This study pioneered an investigation into the viscous dissipative forced convective heat transfer in a parallel-plate channel, partially occupied with a porous medium at the core, under local thermal non-equilibrium condition. Solving the thermal energy equation along the Darcy-Brinkman equation, new exact temperature fields and Nusselt number are presented under symmetrical isoflux thermal boundary condition. Noteworthy is the heat flux bifurcation at the interface between the clear fluid and porous medium driven by viscous dissipation, in cases where the combined hydrodynamic resistance to fluid flow and thermal resistance to fluid conduction is considerable in low Darcy number porous medium insert. However, viscous dissipation does not affect the qualitative variation of the Nusselt number with the fraction of porous medium filling. By using Al2O3-Water nanofluid as the working fluid in a uniformly heated microchannel, partially filled with an optimum volume fraction of porous medium, the heat transfer coefficient improves as compared to utilizing water. The accompanied viscous dissipation however has a more adverse impact on the heat transfer coefficient of nanofluids with an increasing Reynolds number.

Removal of hexabromocyclododecane by carboxymethyl cellulose stabilized Fe and Ni/Fe bimetallic nanoparticles: The particle stability and reactivity in water.

Aggregation of nanoparticles (NPs) can hinder the degradative reactivity of particles towards organic pollutants as it reduces available surface area for reaction. This limitation may be circumvented by applying dispersant to improve colloidal stability of nanoparticle suspension. This study examined the removal of hexabromocyclododecane (HBCD), a recently listed persistent organic pollutant, by carboxymethylcellulose (CMC) stabilized nanoscale zerovalent iron (CMC-NZVI) and bimetallic Ni/Fe nanoparticles (CMC-Ni/Fe) under the influence of suspension chemistry. The mass-normalized removal rate constants of HBCD by CMC-Ni/Fe NPs increased with lower particle aggregation. However, the coating could introduce diffusion resistance as HBCD diffused through the CMC layer to the Fe surface. The activation energy was estimated to be 26.8 kJ mol-1, indicating the overall reaction process was neither surface-limited nor diffusion-controlled. The reactivity of CMC-Ni/Fe NPs toward HBCD was not affected by aqueous initial pH substantially. Common monoanions (Cl-, NO3-, and HCO3-) generally enhanced HBCD adsorption but diminished its debromination. The removal rate did not differ significantly among the studied monoanions over a concentration of 2.5-10 mM except HCO3-. Overall, CMC coating can stabilize Ni/Fe NPs, increase their adsorption of HBCD, provide buffer pH capacity, and overcome common inhibition effects of anions in water. These findings suggested the high potential of using CMC-Ni/Fe NPs for in-situ remediation.

Adaptive tuning piecewise cubic Hermite interpolation with Wiener filter in wavelet domain for scanning electron microscope images.

Image processing is introduced to remove or reduce the noise and unwanted signal that deteriorate the quality of an image. Here, a single level two-dimensional wavelet transform is applied to the image in order to obtain the wavelet transform sub-band signal of an image. An estimation technique to predict the noise variance in an image is proposed, which is then fed into a Wiener filter to filter away the noise from the sub-band of the image. The proposed filter is called adaptive tuning piecewise cubic Hermite interpolation with Wiener filter in the wavelet domain. The performance of this filter is compared with four existing filters: median filter, Gaussian smoothing filter, two level wavelet transform with Wiener filter and adaptive noise Wiener filter. Based on the results, the adaptive tuning piecewise cubic Hermite interpolation with Wiener filter in wavelet domain has better performance than the other four methods.

Effect of carboxylic acids on the properties of zerovalent iron toward adsorption and degradation of trichloroethylene.

Zerovalent iron (ZVI) based technology has been applied to remediate contaminated groundwater and has been paid great attention as an economic alternative. But it is still remains highly challenging to remove chlorinated pollutants such as trichloroethylene (TCE) with ZVI. Low molecular weight carboxylic ligands (formic acid (FA), oxalic acid (OA), and citric acid (CA)) were chosen to study the influence on the performance of ZVI in groundwater, including the morphology of Fe surface and the Fe dissolution. The removal rate of TCE with ZVI in the presence of 30 mM carboxylic groups followed an order of FA > OA > pure water ≅ CA. FA provides protons to promote the surface corrosion and generated more magnetite on the ZVI surface, which was further responsible for a high adsorption of TCE. With the strong complexing ability of OA and CA, passive layers could form dissoluble complexes via a ligand-promoted dissolution process. However, high concentration of OA resulted in Fe oxalate reprecipitated back onto the ZVI surface then inhibited the reactivity of ZVI. The Fe-ligand complexes also have ability to transform TCE depending on their redox properties. It is expected that effectiveness of carboxylic ligands on the ZVI: those low molecular weight carboxylic ligands in groundwater and soil may enhance the reaction efficiency of ZVI by altering the surface characteristics of ZVI. Therefore, the carboxylic ligands could increase the reactivity and the longevity of ZVI.

The influence of carboxymethylcellulose (CMC) on the reactivity of Fe NPs toward decabrominated diphenyl ether: The Ni doping, temperature, pH, and anion effects.

Polybrominated diphenyl ethers (PBDEs) are commonly used brominated flame retardants in many products. They have accumulated in the environment and become widely dispersed. In this study, carboxymethylcellulose (CMC) was applied to modify nanoscale zerovalent iron (NZVI) and bimetallic Ni/Fe nanoparticles (NPs) to prevent NP aggregation. In this study the removal kinetics of the decabrominated diphenyl ethers (DBDE) with CMC-stabilized Fe NPs were evaluated. CMC-stabilized Ni/Fe NPs with an average size of 86.7nm contained metallic Fe0 and reduced Ni. The colloidal stability decreased with a decrease in pH, which was further accompanied by a change in the removal rate of DBDE. Our results showed that anions do not change the removal rates of DBDE, with the exception of 10mM NO3-, which induced the formation of Fe (hydro)oxides on the Fe NP surface, which could further coagulate with DBDE. This study provides important information for our understanding of the influence of CMC coatings on the reactivity of Fe NPs. Because CMC coatings prevent the passivation of Fe in the presence of anions, CMC-coated Fe NPs show potential for the in-situ remediation of PBDEs in the environment.

Concurrent oxidation and reduction of pentachlorophenol by bimetallic zerovalent Pd/Fe nanoparticles in an oxic water.

Under the oxic condition, the most effective removal of pentachlorophenol (PCP) with Pd/Fe nanoparticles (NPs) is demonstrated as compared to the anoxic condition. Concurrent oxidation and reduction of polychlorinated compounds such as PCP by zerovalent Pd/Fe were first observed. The optimal Pd content of the bimetallic NPs is only around 0.54 mg g(-1) Fe. Increases in both dosage of Pd/Fe NPs and temperature enhance degradation rates and efficiency. The activation energy of 29 kJ/mol indicates that the degradation is a surface-mediated mechanism. The removal mechanism also includes adsorption, which explains that the dechlorination of Cl on PCP molecules at ortho and meta positions is easier than that at para position. Overall, Pd/Fe NPs can apply directly to degrade polyhalogenated compounds in water without deaeration.

The effect of electrolytes on the aggregation kinetics of three different ZnO nanoparticles in water.

Nanoscale ZnO particles are receiving increasing attention because they are widely used in commercial products, but they do have potentially hazardous effects. The aggregation behavior of ZnO nanoparticles (NPs) in the environment contributes to the real risk assessment of nano-toxicity, and the real size of the nano-aggregates should be investigated. In this study, the influences of electrolytes on the stabilities of three ZnO NPs were compared: the commercial powder (NP1), the lab synthesized suspension (NP2) and the commercial suspension (NP3). The initial particle size of NP2 and NP3 in water was at a nanoscale whilst NP1 tended to form microscale aggregates. The capping reagents helped to retain their suspension. The stability of ZnO NPs depends on their zeta potential under specific pH value, ionic types and ionic strength. In general, neutralization plays a major role in aggregation. The effect of divalent counter-ions on ZnO NP aggregation was more than that of monovalent ones. The stabilities of NP2 and NP3 were confirmed by the large critical coagulation concentration (CCC) values of these particles. The experimental results also fit the Derjaguin-Landau-Verwey-Overbeek (DLVO) theory. The aggregation of different ZnO NPs is relevant to their basic properties and is influenced by electrolytes, which decreases the possibility of the penetration of NPs into cells to cause toxicity in the environment. An understanding of the basic properties of NPs is crucial for assessing their fate in the environment as well as for setting up usage regulation and treatment strategy.

The reactivity of well-dispersed zerovalent iron nanoparticles toward pentachlorophenol in water.

In order to prevent the aggregation of nanoparticles (NPs), surface modification or the addition of a stabilizer are used for stabilization. However, the real reactivity of NPs is still unclear because of the surface coating. For different physical dispersion methods, the particle stabilization for nanoscale zerovalent iron (NZVI) particles and their reactivity are studied. The particle properties of different preparations and their reactivity toward one polychlorinated aromatic compound, pentachlorophenol (PCP), with different electrolytes are also evaluated. Ultrasonication (US) with magnetic stirring disperses NZVI and Pd/Fe NPs well in water and does not affect the surface redox property a lot under the operating conditions in this study. The well-suspended NZVI cannot dechlorinate PCP but adsorption removal is observed. Compared to shaking, which gives limited removal of PCP (about 43%), Pd/Fe NPs remove 81% and 93% of PCP from water in the US and the US/stirring systems, respectively, which demonstrates that a greater surface area is exposed because of effective dispersion of Pd/Fe NPs. As the Pd doping increases, the dechlorination kinetics of PCP is improved, which shows that a catalyst is needed. With US/stirring, chloride ions do not significantly affect the removal kinetics of PCP, but the removal efficiency increases in the presence of nitrate ions because PCP anions were adsorbed and coagulated by the greater amount of iron (hydro)oxides that are generated from the reduction of nitrate on Pd/Fe. However, bicarbonate ions significantly block the adsorption and reaction sites on the Pd/Fe NP surface with US/stirring. The US/stirring method can be used to evaluate the actual activity of NPs near the nanoscale. The use of Pd/Fe NPs with US/stirring removes PCP from water effectively, even in the presence of common anions expect a high concentration of bicarbonate.

Computerized database management system for breast cancer patients.

Data analysis based on breast cancer risk factors such as age, race, breastfeeding, hormone replacement therapy, family history, and obesity was conducted on breast cancer patients using a new enhanced computerized database management system. My Structural Query Language (MySQL) is selected as the application for database management system to store the patient data collected from hospitals in Malaysia. An automatic calculation tool is embedded in this system to assist the data analysis. The results are plotted automatically and a user-friendly graphical user interface is developed that can control the MySQL database. Case studies show breast cancer incidence rate is highest among Malay women, followed by Chinese and Indian. The peak age for breast cancer incidence is from 50 to 59 years old. Results suggest that the chance of developing breast cancer is increased in older women, and reduced with breastfeeding practice. The weight status might affect the breast cancer risk differently. Additional studies are needed to confirm these findings.

The transformation of hexabromocyclododecane using zerovalent iron nanoparticle aggregates.

Hexabromocyclododecane (HBCD), an emerging contaminant, is a brominated flame retardant that has been widely detected in the environment. In this study, nanoscale zerovalent iron (NZVI) aggregates are firstly used to treat HBCD and its removal under different geochemical conditions is evaluated. HBCD is almost removed from solutions by NZVI, with a kSA of 4.22×10(-3)Lm(-2)min(-1). An increase in the iron dosage and temperature increases the removal rate. The activation energy for the removal of HBCD by NZVI is 30.2kJmol(-1), which suggests that a surface-chemical reaction occurs on NZVI. HBCD is adsorbed on the NZVI surface, where electrons were transferred to HBCD, and consequently forms byproducts with less bromide. Three common groundwater anions decrease the reaction kinetics and efficiency of NZVI. The kobs of HBCD in the presence of anions is in the order: pure water >Cl(-)>NO3(-)≒HCO3(-). The inhibitory effect of these anions may be a result of the possible complexation of anions with the oxidized iron surface. The oxidized sites on NZVI and oxidized species of iron also contribute to the removal of HBCD by adsorption on NZVI from solutions.

Stability of metal oxide nanoparticles in aqueous solutions.

The application of nanoparticles in the processes of making commercial products has increased in recent years due to their unique physical and chemical properties. With increasing amount of commercial nanoparticles released into nature, their fate and effects on the ecosystem and human health are of growing concern. This study investigated the stability and morphology of three metal oxide nanoparticles in aqueous solutions. The commercially available nanoparticles, TiO(2), ZnO, SiO(2), aggregated quickly into micrometer-size particles in aqueous solutions, which may not threaten human health. Their changes in morphology and characteristics were further examined by dynamic light scattering (DLS) method and transmission electron microscopy (TEM). Among the several dispersion approaches, ultrasonication was found to be the most effective for disaggregating nanoparticles in water. For these three selected nanoparticles, ZnO could not remain stable in suspensions, presumably due to the dissolution of particles to form high concentration of ions, resulting in enhanced aggregation of particles. In addition, the existence of dissolved organic matters stabilized nanoparticles in lake water and wastewater for several hours in spite of the high concentration of cations in these real-water samples. The fate of metal oxide nanoparticles in natural water bodies would be determined by the type and concentration of cations and organic matters. Results obtained in this study revealed that the stability of nanoparticles changed under different aqueous conditions and so did their fate in the environment.