Solar energy harvesting and self-cleaning of surfaces by an impacting water droplet

The self-cleaning of surfaces via impacting water droplets is examined pertinent to solar energy applications. The mechanism of spreading and retraction of the impacting droplet onto the dust and cleaned hydrophobic surfaces is considered in the analysis. The spreading factor of the impacting droplet is formulated incorporating the energy balance on the hydrophobic surface. High-speed photography is used to monitor the impacting droplet behavior. The functionalized silica particles coating is introduced towards generating hydrophobic wetting state on the glass surfaces. Environmental dust particles are characterized prior to self-cleaning impacting tests. It is found that spreading rate predicted for the impacting droplet agrees well with that obtained from the experiments. The droplet Weber number incorporated in the experiments does not result in droplet breaking on the surface upon impacting. The dusts are dissimilar in shapes and consist of several elements. Impacting droplet gives rise to cloaking of the dust on the surface during spreading and retraction. Almost all the dusts are removed from the surface through the impacting droplets; however, few dust residues are left on the impacting surface, which cover only 0.03% of the total surface area. Hence, we have demonstrated that self-cleaning of a surface can be achieved by an impacting droplet for renewable energy applications.     

Hydrolysis,polycondensation, and catalytic properties of Ru(II) complex of 3‐4,5‐dihydroimidazol‐1‐yl‐propyltriethoxysilane

The preparation and measurements of some properties of organic–inorganic hybrid materials derived from Ru(II)‐3‐4,5‐dihyroimidazol‐1‐yl‐propyltriethoxysilane inside a polysiloxane network have been achieved. The hydrolysis and polycondensation of Ru(II)‐3‐4,5‐dihyroimidazol‐1‐yl‐propyltriethoxysilane were performed in different experimental conditions, producing a new organic–inorganic silica. The alkoxysilyl groups available were used for the construction of inorganic backbone by the sol‐gel process, and the imidazole group was found suitable for incorporating Ru(II) by coordination. The coordination of metal complex is retained because there is no leaching from the metal complex containing gels. To ensure sufficient catalytic properties, a series of hybrid materials from tetraethoxysilane was prepared. These materials were identified and catalytic activities were tested for cyclization of (Z)‐3‐methylpent‐2‐en‐4‐yn‐1‐ol to 2,3‐dimethylfuran. Heterogeneous Ru(II) catalyst can also be recycled and reused without significant loss of selectivity or activity. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 1329–1334, 2001     

Polyindene/organo‐montmorillonite conducting nanocomposites. I. Synthesis,characterization, and electrokinetic properties

In this study, Na‐montmorillonite was organically modified with cetyltrimethylammoniumbromide (CTAB) and intercalated with in‐situ polymerized indene. Polyindene(PIn)/Organo‐MMT nanocomposites were obtained with three different compositions and coded as: K1: [PIn(94.5%)/O‐MMT(5.5%)], K2: [PIn(92.8%)/O‐MMT(7.2%)], and K3: [PIn(87.9%)/O‐MMT(12.1%)]. These nanocomposites were subjected to full characterization with various techniques. Electrokinetic studies were conducted to reveal the zeta (ζ)‐potential characteristics of the nanocomposites. ζ‐potentials of the materials were observed to decrease with increasing O‐MMT content. The cationic (CTAB) and anionic (sodium dodecylsulfate) surfactants were shifted the ζ‐potentials of the colloidal dispersions to more positive and more negative regions, respectively whereas nonionic surfactant (Triton X‐100) caused almost no change. The pH and temperature were observed to shift the ζ‐potential values of the nanocomposites to more negative and slightly more positive regions, respectively. With the addition of mono (NaCl), di (BaCl₂) and three (AlCl₃) valent salts, the ζ‐potential of the nanocomposites were shifted to more negative, more positive, and much more positive regions, respectively. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Congo red- and Zn(II)-derivatized monosize poly(MMA-HEMA) microspheres as specific sorbent in metal chelate affinity of albumin

Monosize poly(methylmethacrylate-hydroxyethylmethacrylate) [poly(MMA-HEMA)] microspheres (4 μm in diameter) were produced by dispersion copolymerization of MMA and HEMA in an ethanol-water medium. Congo Red was attached to the poly(MMA-HEMA) microspheres, covalently. These Congo Red-derivatized microspheres were characterized by optical microscopy, Fourier transform infrared spectroscopy, and elemental analysis. Then, Zn(II) ions were incorporated by chelating with the immobilized Congo Red molecules. Different amounts of Zn(II) ions [1.2–17.6 mg of Zn(II)/g of polymer] were conjugated on the microspheres by changing the initial concentration of Zn(II) ions and pH. Bovine serum albumin (BSA) adsorption on these microspheres from aqueous solutions containing different amounts of BSA at different pH and ionic strengths was investigated in batch reactors. The nonspecific BSA adsorption on the plain poly(MMA-HEMA) microspheres was very low (0.7 mg of BSA/g of polymer). Congo Red derivatization significantly increased the BSA adsorption (up to 35.8 mg of BSA/g of polymer). A further increase in the adsorption capacity (up to 61.0 mg of BSA/g of polymer) was observed when Zn(II) ions were incorporated. More than 90% of the adsorbed BSA was desorbed in 1 h in the desorption medium containing 1.0M NaSCN at pH 8.0. © 1997 John Wiley & Sons, Inc.     

Fine aggregate and curing temperature effect on concrete maturity

Removal of formwork can be made in a short time by early-strength gain of concrete with heat treatment. The effects of accelerated curing temperature and fine aggregate on early strength as well as the relationships between early strength-28-day strength and strength maturity have been examined. Cube concrete specimens produced with a 10-cm constant slump value, 0.59 w/c ratio, and with two different types of fine aggregate were subjected to three-phase cure processes. These cure processes include a 1-h preheating process after having replaced concrete in the mould, the cure application process, and finally the last waiting period for 2 h that is aimed at minimizing the effects of thermal stresses. Each of the specimen groups was cured at different temperatures for different periods (6 or 18 h). At the end of curing and on the 28th day, cube compressive strengths were determined. Therefore, it was seen that it is possible to estimate 28-day strength beforehand with reasonable accuracy.     

Estimation of the vapour pressure deficit using NOAA-AVHRR data

In this study, the calculation of vapour pressure deficit (VPD) using the National Oceanic and Atmospheric Administration Advanced Very High Resolution Radiometer (NOAA/AVHRR) satellite data set is shown. Twenty-four NOAA/AVHRR data images were arranged and turned to account for both VPD and land surface temperature (LST), which was necessary to calculate the VPD. The most accurate LST values were obtained from the Ulivieri et al. split-window algorithm with a root mean square error (RMSE) of 2.7 K, whereas the VPD values were retrieved with an RMSE of 6 mb. Furthermore, the VPD value was calculated on an average monthly basis and its correlation coefficient was found to be 0.991, while the RMSE value was calculated to be 2.67 mb. As a result, VPD can be used in studies that examine plants (germination, growth, and harvest), controlling illness outbreak, drought determination, and evapotranspiration.     

The Effect of Gd Concentration on the Physical and Magnetic Properties of Bi1.7Pb0.3-xGdxSr2Ca3Cu4O12+y Superconductors

Bi–Pb–Gd–Sr–Ca–Cu–O bulk samples with nominal composition Bi_1.7Pb _0.3-xGd_xSr₂Ca₃Cu₄O_12+y (x=0.01, 0.05, 0.075, 0.10) were prepared by the melt-quenching method. The effects of different Gd doping on the structure have been investigated by electrical resistance, scanning electron micrographs, XRD, magnetization and magnetic hysteresis loop measurements. The magnetization measurements have been carried out as a function of magnetic field for fields up to 5 kOe at temperatures well below the zero resistance temperatures of the annealed samples. It has been found that the high-T_c superconducting phase, (2 2 2 3), is formed in the sample A with concentration x = 0.01, annealed at 840°C for 120 h. However, with increasing Gd³⁺ doping for Pb²⁺ the (2 2 2 3) phase gradually transforms into the (2 2 1 2) phase. The magnitudes of magnetization and initial susceptibility, | M | and | dM/dH|, and the hysteresis loop areas decrease with increasing Gd concentration x and/or temperature T. The fast decreases in | M|, | dM/dH |, and the hysteresis loop areas related to the superconducting volume, with increasing x and/or T seem to imply an existence of flux pinning centres in our samples. In order to support this implication the critical current densities J_c, of the samples, have been estimated at two fixed temperatures, 9 and 30 K. Our data have indicated that J_c decreases with increasing temperature and/or Gd concentration, as expected.     

Structural and Magnetic Properties of Cobalt(II) Complexes of Triphenylphosphine

This work is related to the structural and magnetic properties of the Co(PPh₃)Cl₂ metal complex for different sintering times. The structural and physical properties of the complex have been studied by using SEM, EDX, and magnetization techniques. SEM results clearly demonstrate that the grains of the complex are very well connected to each other and tightly packed. Magnetization measurements with respect to magnetic field and temperature show a paramagnetic behavior above 20 K for the all samples. Furthermore, the susceptibility (χ) as a function of temperature indicates a paramagnetic-antiferromagnetic phase transition with a negative value of the Curie–Weiss temperature, θ. In addition, increasing sintering time appears to also enhance the effective magnetic moment, μ _eff.     

Commercial test kits and the determination of histamine in traditional (ethnic) fish products-evaluation against an EU accepted HPLC method

Although commercial test kits are generally used and/or evaluated for determining histamine in fresh and canned fish, and fish meal, there is little information on their performance and the application for traditional fish products (TFPs), which generally differ in product properties. In this study, three quantitative (Food EIA, Veratox, Histaquant) and four qualitative (Histasure, Histameter, Transia qualitative and semi-quantitative) commercial histamine test kits were evaluated against HPLC method for detecting histamine in several traditional fish products. Among the quantitative kits, Histamine Food EIA showed the best correlation with HPLC method for TFPs (R² = 0.9132) as well as good recoveries ranging between 89 (±4.11)% and 117 (±1.50)%. Although good recoveries were also observed with Veratox kit, poor correlation was found with HPLC. Poor correlation and low recoveries were also observed with Histaquant. Histasure and Transia tube histamine kits showed good agreement with HPLC results. However, the detection limit for Transia qualitative kit is 100 ppm, and for Histasure and Transia semi-quantitative kits can be set to 50 ppm. Therefore, Histasure and Transia semi-quantitative kits are found more suitable for either HACCP monitoring histamine in seafood processing plants or regulatory purposes according to Food Drug and Administration (FDA) legislation for TFPs. However, Transia semi-quantitative kit should be used in caution for histamine cut off values <50 ppm. This study shows that each test kit can represent different performance for determining histamine in TFPs according to product type, and therefore new commercial test kits should be evaluated against an approved analytical method before applications in future for these types of products.     

Changes during fishing season in the fat content and fatty acid profile of edible muscle,liver and gonads of anchovy (Engraulis encrasicolus) caught in the Turkish Black Sea

This study aimed to determine the fat content and fatty acid (FA) composition of anchovy (Engraulis encrasicolus, Linnaeus, 1758) in their edible muscle, liver and gonad during the catching season (between September 2008 and April 2009) in The Black Sea Region, Turkey. The most abundant FAs in all samples were palmitic acid (ranged as 15.93–27.34%) amongst saturated fatty acids (SFAs), oleic acid (10.72–21.37%) amongst monounsaturated fatty acids, eicosapentaenoic acid (EPA) (5.28–14.11%) and docosahexaenoic acid (DHA) (9.83–22.34%) amongst polyunsaturated fatty acids (PUFAs). At the beginning of winter, significant increase in edible muscle and liver’s PUFAs and ∑n3/∑n6 were observed (P < 0.05). The highest contents of ∑PUFAs for muscle and liver were observed in January as 38.52% and 38.82%, respectively, while highest n3/n6 ratios were found in April as 10.13% for muscle and in January for liver samples as 9.15%. This study indicates that anchovy is a good nutritional source for human consumption with high contents of omega 3 fatty acids, particularly during winter. In November, about 130 g of anchovy edible meat is found to be in the satisfactory level for EPA + DHA according to the recommended weekly requirement.